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Koutstaal, Wilma.
The agile mind / Wilma Koutstaal.
p. cm.
Includes bibliographical references and index.
ISBN 978-0-19-536718-8 (hbk. : alk. paper) 1. Thought and thinking. 2. Creative thinking.
3. Divergent thinking. 4. Adaptability (Psychology) I. Title.
BF441.K586 2011
155.2’4—dc23
2011030843
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Contents
Preface xvii
Acknowledgments xix
v
vi CONTENTS
Notes 613
References 639
Index 739
Detailed Contents
Preface xvii
Acknowledgments xix
vii
viii D E TA I L E D C O N T E N T S
I N C R E A S E D FAC IL I T Y AT F L E X I B LY R E M E M B E R I N G R E C E N T E V E N T S AT
DI F F E R I N G L E V E L S OF S PE C I F IC I T Y P O S I T I V E LY C OR R E L AT E S W I T H
FL EXIBL E T HINK ING A ND FLUID R E A S ONING 75
R E T R I E V I N G R E C E N T LY E X PE R I E N C E D E V E N T S AT A S PE C I F IC
V E R S U S A B S T R AC T L EV E L H A S C A R RYOV E R C ON S E Q U E N C E S
F OR L AT E R R E C OL L E C T ION — A N D F OR T H I N K I N G 98
A NA L O G I E S , S I M I L A R I T I E S , A N D S UC H : N O T S O C ON T R OL L E D
(OR AU TOM AT IC) CON T R IBU TOR S TO A DA P T I V E LY CR E AT I V E
A NA L O G IC A L A N D C AT E G OR IC A L PROBL E M S OLV I N G 112
L O OK I N G B AC K 122
E X C U R S ION 2 : L EV E L S OF S PE C I F IC I T Y I N D OU G L A S HOF S TA D T E R ’S
S U B C O G N I T I V E M E C H A N I S M S OF F L U I D T HO U G H T 123
T H E C E N T R A L I T Y OF PE R C E P T UA L A N D AC T ION - R E L AT E D
INF OR M AT ION IN T HINK ING 127
L O OK I N G B AC K 173
E X C U R S ION 3 : A H Y P O T H E T IC A L T R A I N OF T HO U G H T:
PE R C E P T UA L S I M U L AT ION I N A RT H U R C ON A N D OY L E ’S
T H E HO U N D OF T H E B A S K E RV I L L E S 174
E X C U R S ION 4 : S PE C U L AT I N G F R E E LY : G E RT RU DE S T E I N
A N D T H E L E T T E R “ M ” 175
L O OK I N G B AC K 233
EXCUR SION 5: A N EXA MPL E OF DUA L MOT I VAT ION GONE AW RY ? 234
P O S I T I V E E MO T ION S 239
OPE N N E S S T O E X PE R I E N C E , C R E AT I V I T Y, A N D A DA P TA B I L I T Y 269
Openness to Experience, Creativity, Divergent Thinking,
and Orienting Sensitivity 270
Openness to Experience and Adaptive Learning 275
I N T E R E S T, C U R IO S I T Y, A N D VA R IE T Y S E E K I N G 278
L O OK I N G B AC K 280
OP T I M I S M V E R S U S PE S S I M I S M , OV E R C ON F I DE NC E
V E R S U S U N DE R C ON F I DE NC E 291
T RY I N G N O T: I N T E N T IONA L F OR G E T T I N G ,
DE L IBER AT E T HOUGHT S UPPR E S SION , A ND FL EXIBL E
T HINK ING 298
A B S OR P T ION , F L O W, A N D “ H Y P O E G O IC ” S E L F - R E G U L AT ION:
T H E C ON T R OL L E D L O S I N G OF C ON T R OL A N D T H E M E L DI N G
OF T HO U G H T - E M O T ION - AC T ION 307
WOR K I N G W E L L W I T H T H E U N C ON S C IO U S :
INCUB AT ION A ND COMPL EX MULT ICOMPONE N T I A L
DE C I SION M AK ING 313
M OV E M E N T S B E T W E E N H IG H E R L EV E L A N D L O W E R
L EV E L GOA L S: OPPORTUNI S T IC DE SIGN 323
E NC O U N T E R I N G DI V E R SI T Y I N T H E T HO U G H T S A ND
V I E W S OF O T H E R S 327
L O OK I N G B AC K 329
xii D E TA I L E D C O N T E N T S
G OA L N E G L E C T, F L U I D I N T E L L IG E NC E , A N D WOR K I N G
ME MORY: BEYOND PR EF RON TA L CORT EX TO DY NA MIC A N T E R IOR-
P O S T E R IOR A N D ACR O S S - S Y S T E M I N T E R AC T ION S 374
A NA L O G IC A L A N D R E L AT IONA L T HO U G H T: B R A I N C OR R E L AT E S
OF FLUID R E A S ONING 410
I N T U I T I V E PRO C E S S I N G : PA RT I A L LY I N F OR M E D G U E S S I N G ,
PR E DICT ION , A N D G I S T 417
B E T W E E N TA S K S : T H I N K I N G A B O U T T H E PA S T, I M AG I N I N G
T H E F U T U R E , A N D O U R E V E R - AC T I V E , S A L IE NC E - DE T E C T I N G
A N D N E T WOR K - C H A N G I N G M I N D S 428
De t ail e d C on t e n t s xiii
N OV E LT Y, R EWA R D, A N D E X P L OR AT ION : T H E L O C U S
C O E RU L E U S – N OR EP I N E P H R I N E S Y S T E M A N D A DA P T I V E
R E SPONDING TO NOV E LT Y 445
L O OK I N G B AC K 460
S E C ON D - OR M U LT IP L E - L A N G UAG E U S E ( B I L I N G UA L I S M
A ND MULT IL INGUA L I SM) 507
S O C IO E C ON O M IC S TATU S , S T R E S S , A N D B R A I N PAT HS
TO AGIL E T HINK ING 513
E X PE R I M E N TA L I N T E R V E N T ION S A N D M E N TA L AG I L I T Y
IN HUM A N S 539
Notes 613
References 639
Index 739
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Preface
Minds do not exist in a vacuum, nor do brains. We know this, but we as often forget it.
Or it becomes lost in the keenness of our pursuit of more focused questions.
This book attempts to keep mind, brain, body, and environment together.
Listing four things is easy. Consistently respecting their pair-wise and higher order
interrelations is not so easy. But here I have tried, because we must.
We must if we are to fully scientifically understand how agility of mind is possible
and thereby protect and promote the conditions that enable it.
My own aspirations toward such an understanding, as expressed here, have diverse
origins. There are many individuals, some known, others anonymous, including
reviewers of earlier drafts of portions of the manuscript, who have provided encour-
agement, suggestions, and resilient optimism about the worth of the endeavor.
Thanking everyone, colleagues, family, and friends, individually here is not possible.
But there are a few who cannot go unnamed. At Oxford University Press, my original
editor, Catharine Carlin, who from the first recognized the conceptual scope that was
needed and saw how to quietly but surely enable it; also Joan Bossert and Tracy O’Hara
at Oxford University Press, for their help in shepherding through the transition to the
production phase, and Leslie Anglin, Kavitha Ashok, and Emily Perry for their deft attun-
ement to both the small details and the bigger picture in the many stages en route from
an initial manuscript to a printed book. There are also those who indirectly, rather than
directly, helped to make this possible, through their example and support. I am grateful
to my earlier mentors and colleagues at Harvard for uniquely exemplifying grounded pio-
neering intellectual reach: Roger Brown, Randy Buckner, Brendan Maher, Hilary Putnam,
Don Rubin, Dan Schacter, and Anthony Wagner, and to more recent exemplars of intel-
lectual generosity: Steve Engel, Jan Estep, Sheng He, Yuhong Jiang, and Dan Kersten.
I also must thank the students, both undergraduate and graduate, in my classes
and my labs, and my postdoctoral fellows, for their probing questions, their relentless-
ness, and their abiding commitment to inquiry, learning, and teaching. Universities,
research universities in particular, are very special places, and saying so is something
that we need to do more often, lest they become taken for granted and no longer be
environments that allow us all to grow, share, learn, and make “fruitful” (useful,
beneficial, or grounding) newness in the world.
But it is to Jonathan Binks—my lifelong creative partner—that I dedicate this
work. Without his faith, it would not be.
xvii
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Acknowledgments
Selections from “Notes Toward a Supreme Fiction,” (p. 387) and from “Thirteen Ways
of Looking at a Blackbird” (p. 573) reprinted from The Collected Poems of Wallace
Stevens by Wallace Stevens, copyright 1954 by Wallace Stevens and renewed 1982
by Holly Stevens. Used by permission of Alfred A. Knopf, a division of Random
House, Inc.
xix
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The Agile Mind
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1
Agility of Mind and the Integrated
Controlled-Automatic, Specific-Abstract
(iCASA) Framework
In the end I abandoned any attempt at forward planning,
deciding that the best way to operate was to go into the
studio with no preconceived ideas and to take each session
as it came, as freely and spontaneously as possible.
—Oscar Peterson (2002, p. 264)
This is a book about bridges—bridges within, and to, thinking. The material for
the bridges is experimental and observational evidence, from psychology, cognitive
neuroscience, and allied disciplines, regarding the factors that are most likely to foster
what I shall call agility of mind, agile thinking, or mental agility.
Physical agility is characterized by nimbleness, flexibility, and a capacity to rapidly
and aptly alter the position or directional movement of one’s body without losing
one’s balance. Similarly, mental agility entails a readiness and capacity to change our
manner of thinking, or of approaching a situation, endeavor, or problem, without
losing our “balance” in terms of our broader goals and aims. Agility in the physical
sense is especially called upon in circumstances involving unexpected obstacles or
dynamically changing situations. Yet agility is only one of several essential compo-
nents in physical fitness. One also needs endurance and aerobic capacity, and many
factors such as strength, coordination, and learning contribute to physical agility.
All this is also true of mental agility.
Agile thinking involves ways of representing and processing (using) information
and knowledge that is flexibly, creatively, and adaptively attuned to changing circum-
stances and goals. It is thinking that is able to promote and sustain both long-term
and provisional plans and projects in the face of dynamic and more stable environ-
ments, in the midst of uncertainty and ambiguity, and for real-life risks and rewards.
3
4 THE AGILE MIND
Although agility of mind involves many different contributors both internal and
external to the individual, which operate at multiple levels of analysis and multiple
time scales, it can be broadly and fundamentally characterized as reflecting appropri-
ate and adaptive variability of responding on two dimensions. One dimension
corresponds to the processes involved in thought, that is, the “how” of thought, the
ways in which thinking occurs or proceeds. This is the dimension of levels of cognitive
control. The second dimension corresponds to the content of thought, or the “what” of
thought, the “that” to which thinking is directed toward or is about. This is the dimen-
sion of levels of representational specificity.
When we are mentally agile, we are able to draw upon, and to “aptly use,” the full
continuum of cognitive control—ranging from highly deliberate and controlled respond-
ing, thinking, and judgment, on one side, to spontaneous or improvisational, to
automatic or habitual responding, on the other side. Across the many dynamically
changing tasks, situations, and problem spaces that we confront, no one place on the
continuum of cognitive control is invariably ideal: the “right” (optimal, best, most
appropriate) level of control, from highly deliberate and controlled to rapidly inter-
mixed spontaneity and improvisation, to automatic or habitual responding, will
depend on the (unfolding) specifics of the situation. Equally important, when we are
mentally agile we are also able to draw upon, and to “aptly use,” the full continuum of
levels of specificity of mental representations—ranging from the highly abstract (e.g.,
categorical, gist-like, schematic, superordinate) to the exceedingly specific (e.g., item
specific, concrete, episodic, subordinate), as well as any of the numerous “basic-level”
midpoints in between. Inducements and impediments to variation on both of these
dimensions, and how such variation may be realized in the brain, are thus recurrent
themes of the following chapters. Notably, as we will see, apt and wide variation across
these two dimensions is not confined to strictly conceptual content but may apply to
multiple domains of experience: Concepts and memories, yes, but also to diverse aspects
of emotion, perception, motivation, and action.
We already have several concepts in cognitive neuroscience and psychology that
refer to various aspects of flexibly adaptive thinking. Prominent examples here include
executive function, self-regulatory capacity, fluid intelligence, creativity, and resil-
ience. Why propose yet another concept: Do we need another construct? To what end?
As will be developed more fully in the section “Distinguishing Mental Agility,” each of
these example concepts, and associated treatments of thinking, reasoning, and judg-
ment, predominantly emphasizes particularly one side of the representational
content or representational process pairings, and frequently focuses on the benefits
of one of the pair (usually abstraction in the case of representational content, and
controlled processing in the case of representational process). This book attempts to
take a more even-handed and democratic approach, equally often stressing the bene-
fits and the potential hazards and costs of reliance on either controlled or automatic
processing, and either abstract or specific representations. It also centrally draws
attention to the factors that enable—versus impede—our appropriate and adaptive
movement between varying levels of cognitive control and varying levels of specificity
across different domains of experience.
So one answer to the question of why we need another construct is that mental
agility is a broader, more encompassing construct that emphasizes the important but less
Ag il ity of Mind and t h e iC ASA F ram e w ork 5
Self-
Executive regulatory
function capacity
Mental agility
Fluid
Creativity intelligence
Resilience
examined questions of how, when, and why we move between different levels of cognitive
control and between differing levels of representational specificity. Figure 1.1 provides a
simple schematic of this way of “distinguishing mental agility”; a more formal treat-
ment of these related but narrower concepts is provided later in this chapter.
A second answer to the question of why we need a construct of mental agility might
itself be couched in examples, illustrating the referential domain of the more abstract
concept with particular instances. Let’s here bring to mind some examples—examples
that are exaggerated and rather simplified for the sake of demonstrative clarity, but
not nonsensical. Imagine a person who is inveterately creative—someone who is
always generating novel ideas and new possible approaches to situations, seeing
alternative ways to construe a situation; she is an endless source of innovations in
thought and action. Would such endlessly creative cognitive processes prove uniformly
beneficial? What if the old, conventional or habitual method of approach in a given
context was, all things considered, the best approach, even though it had been used on
numerous occasions previously? We have likely encountered individuals who are
somewhat like this—or persons of the opposing predisposition: those who ever stick
closely to the “tried and true,” varying little, relying on habitual or proceduralized
approaches to most of the projects they pursue, and who are distinctly uncomfortable
with variations or change. This “habit-bound” person may well demonstrate judg-
ments and behaviors in some situations that we evaluate as more appropriate (more
fitting) than those shown by the inveterately creative individual. Nonetheless, we also
would recognize that the habit-bound person (perhaps of the “good fences make good
neighbors” sort, gently or perhaps not-so-gently critiqued by the poet Robert Frost in
the poem, “Mending Wall”) is neither fully realizing his possible potential for experi-
ential growth and learning nor approaching even mundane and apparently inconse-
quential activities in ways that are optimal.
Now imagine three other persons: One person can never “let go” but must
always be “in control,” explicitly aware of all the plans for the day and for the next five
minutes as well as all the steps to be taken to get there, and who is decidedly uncom-
fortable with spontaneity or experiment; a second person, who never seems to really
get the “big picture” but is always lost in a dense tangle of details and specifics and
6 THE AGILE MIND
questions of how, precisely, to do this and how to do that, never stopping to articulate
what the larger goal is; last, a third person of the opposite tenor—one who
never seems to attend to anything but the “big picture,” who seems to entirely miss the
concrete and detailed goings-on and “hands-on how-to” that surround him, perhaps
modeled on the chronic worrier who continually ruminates about such abstract and
underspecified questions as “What if I fail?”
Clearly, each of these persons is a caricature, but the caricatures point to different
predominant predispositions that we can have both for adopting particular levels of
cognitive control (e.g., highly deliberate and planned vs. spontaneous and improvisa-
tional vs. habit-bound and automatic) and also for adopting particular levels of
representational focus, construal, or specificity (e.g., detailed and specific vs. basic
level vs. general and abstract). The caricatures also emphasize that getting stuck at any
one of the points of either the level of control or the level of specificity continuum can
prove problematic, interfering with flexibly adaptive thinking and judgment.
There is no existing concept that captures such a capability for flexibly adaptive
thinking and responding, involving the ability to adeptly move across both varying
levels of specificity and varying levels of control as circumstances require; as devel-
oped later, even comparatively broad concepts such as that of resilience, or executive
function, denote narrower aspects or subsets of this broader more encompassing sort
of “adroitly adaptive” flexibility. A person who is mentally agile is one who is able to
avoid the hazards and costs of each of these caricatures: He or she is able to draw on
habitual or repeated responses when this is appropriate, and to move up, or down, in
level of action identification (e.g., focusing on how vs. why) as external circumstances
demand. He or she is also able to move into states of defocused receptive attention
and cognitive/perceptual processing that allow mainly associative, intuitive connec-
tions and pattern recognition to emerge, either when “stuck” due to having reached an
impasse when using deliberately controlled processes, or when broader associative
search in a problem space is needed, yet can also resume deliberate and/or analytical,
feature-based problem-solving efforts at multiple points. In brief, he or she is neither
excessively or too unremittingly overcontrolled nor unremittingly undercontrolled; he
or she is neither an unrelenting skeptic of intuition and spontaneous judgments nor
an uncritical acceptor of its products or process.
Although representational content and representational processes may be
construed and categorized in different ways, as noted, they have very often been
characterized in terms of the extremes of the abstract versus the specific in the case of
representational content, and of controlled versus automatic in the case of representa-
tional process. Many other pairs of terms also have been used, with differing connota-
tions and purposes, but broadly mapping to generally similar territory. In the case of
representational content, other terms include category versus exemplar, gist versus
verbatim, and structural versus surface; in the case of representational process, other
terms are analytic versus experiential, reasoning versus intuitive, and System 2 versus
System 1. These terms and distinctions among them, and also the manner in which
they tend to explicitly or implicitly conflate levels of control and levels of specificity, are
more formally considered in later sections of this chapter.
Thus, one way that this is a book about bridges in, and to, thinking is that it brings
together, in one conceptual space, several more discrete and narrower concepts, each
Ag il ity of Mind and t h e iC ASA F ram e w ork 7
of which treats aspects of adaptively creative thought and judgment, but that
are typically considered separately or singly (e.g., creativity and resilience, or creativity
and executive function). Notably, however, this is undertaken in an emergent or
bottom-up manner. The chapters typically begin not with constructs but with
concrete examples of conditions under which agile thinking is, or is not, observed in
relation to each of the four interpenetrating domains of representations: memory
and concepts, perception, action and motivation, and emotion. This rich and varied
database, gathered and probed in Parts I and II of the book, then provides grounding
for the four chapters of Part III, which focus on the multiple contributing brain
systems and possible mechanisms within the brain that contribute to our capacity
for mental agility. The possible substrates and correlates of mental agility in the brain
are explored in a more focused, “paradigm-specific” manner in the initial half of
Part III (Chapters 8 and 9); these chapters concentrate on controlled experimental
findings from neurophysiology (e.g., single-cell recordings), brain imaging (e.g., func-
tional magnetic resonance imaging), neuropsychology (e.g., findings from patients
with semantic dementia, and patients with lesions to distinct areas of prefrontal
cortex), and some related neurochemical explorations that have informed our under-
standing of the brain bases of levels of control, levels of specificity, and adaptive
modulation of both levels of control and levels of specificity. The ways in which our
broader (often messier, more complex, multimodal, and dynamic) experiential
environment modifies the function, structure, and connectivity networks of the brain
across time is taken up in the latter half of Part III. In these later chapters, we first
concentrate on evidence from indirect observational and longitudinal studies (Chapter
10) and then turn to consider direct experimental investigations (Chapter 11) that
illuminate how the environments we create, choose, or find ourselves within, can
either make, and sometimes also unmake, “brain paths” to agile thinking.
A second, related way that this is a book about bridges, then, is in terms of the
domains of evidence taken into its purview: Some of the bridges are across scientific
and academic content areas, particularly across the many varied specializations and
subspecializations of psychology, cognitive neuroscience, and allied disciplines that
systematically explore cognition and behavior, with corresponding differences in
methodologies and conceptual approaches. These “data-rich” bridges also substan-
tially connect the more narrowly construed cognitive and conceptual aspects of think-
ing, such as might be emphasized in a typical research treatment of thinking and
problem solving, to the much broader aspects of ourselves as situated “minded” beings,
temporally, materially, and motivationally interfacing with the world around us. On
the relatively “interior side” those aspects include not only domains of what we may
prototypically think of as involving thinking or mental representations and mental
processes—particularly memory, categorization, and concepts—but also perception,
emotion, and motivation, as well as several interrelated dimensions of personality or
temperament. On the relatively “exterior side,” those broader aspects also include
actions, which emerge at the immediate interface between our mental and motiva-
tional world and the physical world, and a vast and continually changing array of
environmental contexts, not only physical but also symbolic, social, and cultural,
which may either encourage and support, or block and undermine, creatively adaptive
thinking. And in the middle of all this—neither entirely on the interior nor on the
8 THE AGILE MIND
exterior side but itself the substrate and “home” of thought and the self—is that
biologically complex, amazingly powerful, tremendously versatile computational and
representational processing entity that we know as “the brain.”
Given that we, and our brains, are “home” to both varying levels of specificity of
representational content, and varying levels of control with regard to representational
process, we need to find ways to pragmatically, conceptually, and empirically integrate
them in our treatments of cognition so as to maximize our potential capacity for agile
thinking. As developed later, the framework proposed here seeks to begin to do just
that. Drawing on the Spanish and Italian word casa, meaning variously house or home,
mansion, cottage, or dwelling, it is called the integrated Controlled-Automatic,
Specific-Abstract framework, or “iCASA” framework.
◊ Our environment can both externally support, and internally enter into, our
representational interface with objects, events, and ideas so that portions of think-
ing are situated “in the world” as well as “in the head.” Our environment, broadly
construed, including the activities and interests that we pursue on a day-to-day
basis and across our lifetimes, continuously and reciprocally influences the
representational processing/representational content space that we are in, and the
representational and processing networks and interconnectivities of our brain.
Environmental enrichment and diversity provide both impetus and essential
matter (grounds or substance) for agile mind/brains and agile thinking.
Content (LoS)
Abstract
Emotion
Perceiving
Process
(LoC) Controlled Automatic
Concepts Acting
Representational
Specific
accessibility
Brain substrates
Experiential environment
between. Levels of control (LoC) can vary from the extremely controlled (deliberate,
systematic, intentional, conscious) to the automatic (nondeliberate, habit-based,
nonintentional, nonconscious, or preconscious), with an intermediate zone that might
be designated as the spontaneous, and involving receptively attuned, diffuse attention
that may nonetheless be broadly constrained by one’s goals and aims.
An essential clarification: Although, in Figure 1.2, there is one axis for LoS and one
axis for LoC, bounded at the extremes by “abstract” versus “specific” and “controlled”
versus “automatic,” this is a conceptual simplification in two important respects. First,
the neurobiological and cognitive processes that support automatic versus controlled
processing are not “one and the same” and so aspects of both automatic and controlled
cognitive-computational functions can occur in parallel, or simultaneously (though
what is within conscious awareness at a given moment may predominantly reflect
controlled or automatic/spontaneous “outputs” into thought). Second, and relatedly,
both differing levels of control and differing levels of specificity may be present simul-
taneously, or in parallel, particularly with respect to the different “domains” of memory
and concepts, perception, action and motivation, and emotion. Figure 1.2 attempts to
convey this possibility through the only partially overlapping spheres for these
various domains, with the dashed or broken lines in the spheres also denoting
the somewhat permeable and indistinct boundaries of the domains. Additionally,
as schematized in Figure 1.3, both our predominant processing approach (controlled
vs. automatic) and our predominant level of representational specificity (specific vs.
abstract) in each of the domains may dynamically change across time.
Acting
LoS Emotion
Perceiving
Concepts
Concepts
Acting
LoC
Perceiving
Emotion
Emotion
Perceiving
e
Tim
Concepts Acting
matter is treated, despite the absence of any clear and direct cross-referential
identities at the “literal” level of objects or forms.
Within the realm of motivation and action, more specific representational content
might involve greater emphasis on the mechanics or implementation of our goals or
intended actions (the “how”), whereas more abstract content stresses our purpose, the
implications, or the consequences of the action (the “why”) (e.g., Freitas, Gollwitzer, &
Trope, 2004; Vallacher & Wegner, 1987, 1989). Specific representational content might
also be more perceptually immediate, temporally and spatially near or present rather
than distant in time or space (e.g., Liberman & Trope, 2008; Trope & Liberman, 2003,
2010). In contrast, abstract representations in action and motivation might involve
temporally and spatially distal content, cross-situational relevance, longer term and
less immediately “salient” interests or values. Similarly, representational content of
emotions might vary between very impressionistic/global assessments of value or
potency—good/bad, to-be-approached/to-be-avoided, strong/weak (e.g., Barrett et al.,
2001; Feldman, 1995)—to highly differentiated and subtle characterizations involv-
ing multiple layers of complex intimations of responsibility and desire and fear and
hope (e.g., the emotions of Maggie Verver in Henry James’ novel, The Golden Bowl).
The notion of representational specificity can be alternatively construed through
what Mercado (2008) has termed “representational resolving power.” In a proposed
broad account of neural and cognitive plasticity, Mercado assumes that “neural plastic-
ity contributes to cognitive plasticity and intelligence but only to the extent that reorga-
nization increases the brain’s capacity to resolve stimulus representations.” More specifically,
developing both the notion of what comprises a stimulus representation and why
representational resolution is so critical, he states that:
The term stimulus representation is used here to refer to neural activity evoked
either by sensory receptors or by the initiation of movements and thoughts.
Stimulus representations indicate that particular environmental and inter-
nal states have occurred (or are about to occur), and they thus represent
those states. […] an organism’s representational resolving power constrains
what that organism can learn about events. In particular, an individual that
cannot distinguish two stimulus representations cannot learn to respond
differentially to the events that are associated with those representations.
Consequently, an organism’s cognitive plasticity is limited by the capacity of
its brain to resolve stimulus representations […] referred to as representa-
tional resolution. (Mercado, 2008, p. 111)
Evidence to be reviewed here will suggest that individuals may possess multiple
coexisting (often partial) representations of a given stimulus or relation that may
complement but also sometimes compete with one another. Although not necessarily
endorsing all of the assumptions of the position known as “neuroconstructionism,”
the argument made from that position regarding the developmentally unfolding,
successively constructed and continually modified, and context-dependent nature of our
mental representations is very much in line with, and broadly meshes with, the views
developed here. A central tenet of that perspective is the context dependence of the
emergence of representations.
14 THE AGILE MIND
likewise assume that we can flexibly and adaptively adjust the extent to which we rely
on fuller, versus more partial, internal representations for thought and action.
overall or global similarity” such that, for example, a symbolic rule might “single out
one or two specific features of an object to be used in categorization, based on concep-
tual knowledge of the category,” whereas associative processing “categorizes objects
nonanalytically, on the basis of their overall similarity to category prototypes or
known exemplars” (E. R. Smith & DeCoster, 2000, p. 112).
From this overview of dual-process accounts, it is clear that dual-process accounts
frequently have not differentiated between levels of control and levels of specificity
and, instead, implicitly or explicitly couple or “pair” a given level of control (e.g., auto-
matic or habitual responding) with reliance on a particular level of representational
specificity (e.g., gist-based or heuristic processing). This is problematic in that it does
not accommodate perhaps less salient but still often observed alternative “pairings”
such as automatic responding that is based on highly specific exemplars, instances, or
episodes. An excellent example here involves intuitive processing. (Another example
is provided by the notion of “event files” proposed by Hommel, 1998, 2004, 2009, and
recent findings—such as those reported by Horner and Henson, 2009; Race, Badre,
and Wagner, 2010; Waszak, Hommel, and Allport, 2003—demonstrating that the
perceptual, conceptual, and/or response features present during any given moment
of task performance may automatically be integrated into “event files” and that,
depending on circumstances, matches or “partial matches” of such specific episodic
features may either facilitate, or impede, performance. Event files are considered in
the later section of this chapter on “Convergent Theoretical Perspectives on
Automaticity and Multiple Gradations of Levels of Specificity”).
Although intuition is frequently grouped with reliance on general simplifying
heuristics or rules of thumb (such as “take the best,” e.g., Gigerenzer & Goldstein,
1996), not all intuitive judgments rely on such broad heuristics: Intuitive processing
may also draw upon particular (specific) exemplars or instances from memory and be
based on extensive learning or expertise. The distinction between intuition that is
grounded in “simplifying” heuristics, versus intuition grounded in the memory-based
retrieval of similar individual cases derived from extensive experience, is proposed by
Daniel Kahneman and Gary Klein (2009) as an important factor differentiating two
contrasting approaches to intuition. On the one hand, and perhaps most well known,
there is the “heuristics and biases” approach to judgment and decision making, with
its corresponding emphasis on the many errors to which intuitive or automatic
judgments are prone (e.g., Kahneman, 2003; Kahneman, Slovic, & Tversky, 1982). On
the other hand, there is the expertise-based approach to intuition, typified by the
naturalistic decision-making approach of Klein and colleagues (e.g., G. A. Klein, 1993,
2008; Kaempf, Klein, Thordsen, & Wolf, 1996). The latter more often emphasizes,
instead, the highly skilled intuitive accuracy of trained professionals in certain com-
plex domains such as firefighter commanders in the field or experienced nurses in a
neonatal intensive care unit.
The exemplar-based approach to skilled intuition is close to that described by
Herbert A. Simon (1992, p. 155), according to which intuition commonly describes a
problem-solving or question-answering performance that is rapid and for which “the
expert is unable to describe in detail the reasoning or other process that produced the
answer.” Simon describes this process as essentially one of pattern-based recognition:
“The situation has provided a cue; this cue has given the expert access to information
18 THE AGILE MIND
stored in memory, and the information provides the answer. Intuition is nothing more
and nothing less than recognition.” As stated by Kahneman and Klein, the naturalistic
decision making and heuristics and biases approaches:
… share the assumption that intuitive judgments and preferences have the
characteristics of System 1 activity: They are automatic, arise effortlessly,
and often come to mind without immediate justification. However, the two
approaches focus on different classes of intuition. Intuitive judgments that
arise from experience and manifest skill are the province of [naturalistic
decision making], which explores the cues that guided such judgments and
the conditions for the acquisition of skill. In contrast, [heuristics and biases]
researchers have been mainly concerned with intuitive judgments that arise
from simplifying heuristics, not from specific experience. These intuitive judg-
ments are less likely to be accurate and are prone to systematic biases.
(Kahneman & Klein, 2009, p. 519, emphasis added)
These approaches further agree that genuinely skilled intuitive judgments (rather
than, for example, simply “lucky” intuitive judgments that turn out to be correct) rely
on a number of essential preconditions. Most notably, genuinely skilled intuitive judg-
ments require, first, the presence of an environment with sufficient regularity that it pro-
vides “adequately valid cues to the nature of the situation”—that is, cues to the causal and
statistical structure of the relevant environment, even if the individual cannot explic-
itly articulate those cues or their interrelations. Second, genuinely skilled intuitive
judgment also requires extensive practice, and multiple related factors, such as adequate
opportunities for feedback and for learning from mistakes (see Fadde, 2009, for applica-
tions to the domain of education and sports training, such as rapidly recognizing base-
ball pitches). According to the recognition-primed decision model, people use their
experience in the form of a “repertoire of patterns” to select a specific possible course
of action, that they also then mentally simulate to see how that particular action would
play out in their current specific situation (modifying or revising it only as necessary):
These patterns describe the primary causal factors operating in the situation.
The patterns highlight the most relevant cues, provide expectancies, identify
plausible goals, and suggest typical types of reactions in that type of situa-
tion. When people need to make a decision they can quickly match the situ-
ation to the patterns they have learned. If they find a clear match, they can
carry out the most typical course of action. In that way, people can success-
fully make extremely rapid decisions. The [recognition-primed decision-
making] model explains how people can make good decisions without
comparing options. (G. A. Klein, 2008, p. 457)
Behaviors
e
tiv
ec
Aff
Cognitive
Brain
areas A1 A2 A3 A4
Network 1 Network 2 Network 3
affect or emotion may play as an input and/or output to the process (Glöckner &
Witteman, 2010). The proposed classification includes associative intuition, which is
based on simple learning-retrieval processes, such as classical conditioning, social
learning, or implicit recording of frequencies and values; matching intuition, which
is based on comparisons with prototypes/exemplars; accumulative intuition, which is
based on automatic evidence accumulation in which an overall cognitive and affective
evaluation is compared with a threshold; and constructive intuition, which is based on
the construction of consistent mental representations, and involving processes such
as accentuation of evidence, and coherence shifts (see Glöckner & Witteman, 2010,
for additional discussion especially with respect to dual-process accounts of cognition
and the contributions of affect to intuition).
Ag il ity of Mind and t h e iC ASA F ram e w ork 21
Three-year-olds know the first pair of rules, and they know the second pair of
rules, but they have difficulty “stepping back” from their knowledge and
reflecting on the rule pairs and their relation. […] As a result, the pair that
they select is determined by relatively narrow considerations, such as the
way in which the question is asked or the way in they have approached the
situation in the past. […] What these children fail to do is distance them-
selves sufficiently from a particular way of conceptualizing a card so that
they can select the right conceptualization when the time comes. […] Just as
physical distance provides a panorama, psychological distance allows
children to put each perspective into a larger context. (Zelazo & Frye, 1998,
pp. 123–125)
This position suggests that greater (deliberate, explicit) cognitive control may be
achieved through the development of an abstraction over the lower level rules that
the individual knows and understands. However, as also in the case of flexible rule use
in adults, there are also additional factors that may be at play in determining when,
and if, a child may flexibly change between different categorization rules in response to
changed instructions or goals, such as the comparative strength (vs. weakness) of the
representations that are called upon by the task (e.g., Munakata, 2001; cf. Cleeremans
& Jiménez, 2002; Farah et al., 1993; Kinsbourne, 1988), and the ease with which nec-
essary representations can be activated. For example, using a newly developed switch-
ing task, Chevalier and Blaye (2008) showed that at least some of the preschooler’s
errors that appear to be “perseverative errors” may instead reflect a difficulty in activat-
ing a representation that was previously ignored. If the stimuli have multiple dimen-
sions, to effectively sort by one dimension, such as color, then the not-currently-relevant
shape-sorting rule must be suppressed or inhibited. However, this suppression may
later need to be “undone” if the rule again changes to “shape,” and reactivation of the
shape rule may not succeed. This is consistent with a revised version of the Cognitive
Complexity and Control Theory (CCC-r; Zelazo et al., 2003) that proposes that
“children experience switching difficulties both because they ‘are unable to unselect
the previously relevant rules’ and because they are unable to ‘redirect their attention to
the rules that they previously ignored’” (Chevalier & Blaye, 2008, p. 351).
Additional contributors to whether children will demonstrate cognitive flexibility
in a context requiring contextually determined access to different rules also must be
taken into account—for instance, broader social-interactional factors, including social
support, such as reminders to “think about” the current rule before responding in
cases where the rule has switched. Intriguingly such reminding was not helpful, and
indeed detrimental to children’s performance in cases where the rule did not switch.
It is as though reminders to follow a rule when one is already doing so comprises a sort
Ag il ity of Mind and t h e iC ASA F ram e w ork 25
of “reminder overkill” (Deák, Ray, & Pick, 2004, p. 398) that can detract from one’s
performance—perhaps because such reminders normally signal that one should
increase one’s vigilance or attention to the situation at hand, when doing so in this
case is not necessary and may, paradoxically, lead to second guessing and changing
one’s initially correct response to an incorrect response.
Oscillatory Range
A fundamental feature that enables agile thinking is our “oscillatory range” on the two
dimensions of representational specificity (abstract-specific) and representational
processing (controlled-spontaneous-automatic). Oscillatory range clearly involves a
quantitative aspect—we can move between highly specific to highly abstract modes of
thinking and reasoning, and various intermediate levels of abstraction in between.
Yet, under certain conditions, such as in the cases of clinical depression or chronic
worry, individuals may become “stuck” at a relatively abstract and predominantly
verbal level of processing. There are also important learning-related, emotional, and
individual differences factors, for example, that may make adoption of a given level of
abstraction more likely.
Equally important is that oscillatory range essentially involves a temporal compo-
nent. Oscillation implies movement in time. Our “placement” on the two dimensions
of representational specificity and representational processing is not fixed or static:
We are continuously moving on both of these dimensions, increasing or relaxing
effortful control, increasing or decreasing the level of detail or abstraction with which
we represent (re-present) our thoughts and actions. Oscillation may occur both at a
relatively momentary or transient temporal scale (e.g., briefly looking up from a
demanding period of writing to look out of the window) and in relatively more
prolonged extensions of time (e.g., phases of half an hour or more, when one takes a
walk, gardens, or engages in routine activities such as taking a shower or meeting
one’s household responsibilities). These might be referred to as micro- and macro-
oscillations, respectively. As characterized later in the chapter, especially with respect
to Figure 1.6 in the introductory overview section on functional and connectivity
mapping of the brain, and as further outlined in Chapter 9, these oscillations may
both reflect, and be based upon, corresponding changes in the predominant brain
networks that are active at varying times—reflecting dynamic interactions between
central executive or “task-active” networks, and what have been termed the “default
mode” and “salience-detecting” networks of the brain.
A perhaps less immediately obvious but also equally important component of
oscillatory range involves the domains in which it operates. Although our movements
between varying levels of representational specificity (abstract-specific) and of repre-
sentational process (controlled-spontaneous-automatic) clearly involve movements
in the realms of concepts, ideas, and memory, both of these dimensions of represen-
tational process and of representational control also apply to the domains or modali-
ties of perception, action and motivation, and emotion. We can categorize perceived
objects and events at many different levels of specificity and in highly automatic or
much more attention-demanding and effortful ways. Likewise, we can construe our
26 THE AGILE MIND
actions or “what we are doing” in very concrete, “how”-oriented terms (e.g., I am now
pressing keys on the keyboard) or very abstract, “why”-oriented terms (e.g., I am now
attempting to extend your notions of the ways in which abstraction-specificity play
out, not just in the realm of thinking and reflection, but in experienced realms of
action-motivation, emotion, and perception).
There is growing convergent evidence, several key portions of which are examined
in the following chapters, that our movements along the dimensions of representa-
tional specificity (abstract-specific) and of representational process (controlled-spon-
taneous-automatic) in any one of these domains—memory and categorization,
perception, motivation and action, or emotion—may have clear and significant influ-
ences on our performance in other domains. The domains themselves are conceptually
distinct but, in practice, highly interconnected (cf. Figure 1.4). For instance, we will
see that mild increases in positive affect can lead individuals to adopt broader, more
inclusive, conceptual categorizations, and that movement from a deliberative state
regarding whether or not to perform a given action to an implementation state leads
to increased focus on detailed, specific aspects relating to the to-be-implemented
action. And the level of specificity with which we identify “what we are doing”
(concrete vs. abstract) may alter the degree to which we are likely to be distracted by
intervening events or stimuli, and the likelihood that we will return to an activity after
a disruption or upon encountering obstacles.
Other investigators, such as Shimamura (2000) and Miyake et al. (2000) focus on
similar functional components of executive capacity and executive control. In his
dynamic filtering model, Shimamura (2000) proposes that four executive control
processes support the self-regulation of behavior: selecting—that is, focusing
attention on particular aspects of the mental or physical environment; maintaining—
that is, sustaining goals or other relevant information in an activated state; updating
involving the manipulation of information in working memory, and rerouting
28 THE AGILE MIND
involving switching from one task or mental set to another. The factor analytic
work by Miyake et al. (2000) supports three moderately distinct executive control
functions: inhibiting prepotent responses, updating working memory, and set shifting or
rerouting (cf. note 5).
The notion of self-regulatory capacity has some overlap with that of executive
capacity and executive control, particularly the aspect relating to the suppression of
inappropriate responding. Self-regulatory capacity denotes the ability to override and
alter undesirable responses (e.g., Baumeister et al., 1998; Muraven, Tice, & Baumeister,
1998) across a broad range of behavioral and interaction contexts, ranging from
regulating one’s diet or drinking, or one’s study and writing behaviors, to engaging in
regular exercise, showing financial prudence, and appropriately restraining sexual or
other impulses. More formally, in their review of different ways of subdividing atten-
tional processes, Raz and Buhle (2006) defined self-regulation as “the ability to manip-
ulate one’s own emotions, thoughts or actions on direction from the self or another
person” and the more specific process of emotional regulation as “the reduction,
increase or maintenance of an emotional response (for example, fear, anger, or plea-
sure) on the basis of the actions of the self or others” (Raz & Buhle, 2006, p. 368).
In each of these characterizations, there is a strong emphasis on the “top-down”
application of strategies and processes to work toward and define specific
aims—where top-down effects themselves are defined as “controlling, regulating, or
overriding a stimulus-driven or other bottom-up process by such factors as attention
or expectation” (Raz & Buhle, 2006, p. 369). In contrast, there is relatively less room
for, and little explicit consideration of, modes of processing that are more “broadly
receptive” and open to information and input that is not directly relevant to such
“top-down” goals. Yet, in the longer term, and from a broad perspective, individuals
who are not able to also at times adopt modes of processing that are less controlled
and less deliberate, will not maximally capitalize on cognitive and neural-network
resources. There is no agreed-upon term in common use that encompasses the notion
that we need a facility in both controlled and less controlled modes of processing,
and the capability to move between these in response to changing contexts and
constraints.
As developed particularly in Chapter 5, perhaps one of the closest concepts to
mental agility is the developmental construct of resilience or ego-resilience. For exam-
ple, according to J. Block and Kremen:
In the memorable phrasing of J. Block and Kremen (1996, p. 351): “It can be said
that the human goal is to be as under-controlled as possible and as over-controlled as
necessary. When one is more under-controlled than is adaptively effective or
more over-controlled than is adaptively required, one is not resilient.” Likewise,
earlier J. H. Block and J. Block (1980, p. 44) observed that, “extreme placement at either
end of the ego-control continuum implies a constancy in mode of behavior that, given
a varying world, can be expected to be adaptively dysfunctional.” However, this framing of
resilience focuses exclusively on levels of control, whereas agility of mind also entails
the adaptive traversing of varying levels of specificity of mental representations, as
needed. As will be argued throughout this book, to fully understand creatively
adaptive thinking we need to consider the continual interplay between both levels of
representational control and levels of representational specificity.
Another closely related construct is that of “creativity.” Creativity often has
been broadly defined as “the ability to produce original and appropriate problem
solutions,” but in the problem-solving domain, it has been conceptualized particularly
as involving “cognitive flexibility”:
Surely artists cannot predict the full form that their works will take anymore
than competent speakers can control all the implications and meanings of
their words; any process of representation will hold surprises. But to glorify
the degree of surprise and unconsciousness within an act of signification, at
the expense of the element of control and deliberation, seems somewhat
perverse. (Shiff, 1986, p. 219)
A further broad concept that is closely related to agile thinking is “fluid intelli-
gence.” Fluid intelligence specifically refers to the ability to reason about and to solve
particularly new problems independently of previously acquired knowledge. Cattell
defined it as the ability to discriminate relations, and it is often seen as influencing
novel problem solving and adaptation to novel situations, or so-called on-the-spot
reasoning (J. R. Gray & Thompson, 2004, p. 471). Thus, the Cattell Culture Fair test
was developed to measure “individual intelligence in a manner designed to reduce, as
much as possible, the influence of verbal fluency, cultural climate and educational level”
(R. B. Cattell & Cattell, 1960, p. 5). In contrast, “agile thinking” might apply both to
highly familiar, well-learned, and even mundane contents and contexts (both verbal and
nonverbal) as well as novel never-before-experienced elements of situations. Additionally,
fluid intelligence is often strongly positively correlated with several measures of
controlled processing, particularly working memory and executive processing,7 whereas
the term “agile thinking” is intended to capture not only controlled but also adaptive
movements between varying levels of control—and noncontrol—in our thought.
There also is a more communicatively or socially responsive reason to focus on
“agile thinking” rather than “fluid intelligence.” The term “intelligence” for many
people likely immediately evokes notions of “testing” in a fairly narrow or literal
(school-related) sense, and it also may be associatively linked to possibly negative
and/or emotionally volatile issues of inherited ability, and so on. By contrast, the
concept of “agile thinking” is less likely to be prejudged as uninteresting or unhelpful;
it may be more widely appealing and seems more broadly applicable than does “fluid
intelligence” or “executive function.” Indeed, this book will aim to make the case that
we do need a new, more integrative and overarching term to help us think in novel
ways about what may enable us to—more often and more successfully—engage in
creative (innovative, adaptive, flexible) thinking.
Because the new stimuli revive old networks and become associated with
them, the new cognits become the extension of old ones. Thus, there is no
such thing as the genesis of a completely new percept or memory, either in
the brain or in the phenomenic world of consciousness. In their formation,
Executive memory Perceptual memory
Conceptual Conceptual
Plans Semantic
Programs Episodic
Acts Polysensory
Phyletic Phyletic
motor sensory
Sm
Tas
Tou
Aud
Visi
Actions
ell
te
ch
on
ition
(behavior, language)
RF
31
2
6
5
8
9 7
4
9
46 40
39
10 6
45 44
43 19
41 18
42
11 47 22
37 17
38 21
20
32
Ag il ity of Mind and t h e iC ASA F ram e w ork 33
new cognits retrieve old ones and become part of them, in a continuous
dynamic process of interaction between history and new experience that
takes place in the neuronal networks of the posterior cortex of association as
in the course of life the organism interacts with its environment. (Fuster,
2006, p. 129)
Precisely where, and how widely distributed in the brain, a newly formed cognit
will be depends on many factors, including the sensory qualities involved in the expe-
rience (e.g., visual vs. auditory information), and also the complexity and generality of
the experience and the associations it evokes. Whereas more concrete sensory cognits
will predominantly reside in sensory and parasensory association areas (e.g., inferior
temporal cortex in the case of vision, superior temporal cortex for audition, and
anterior parietal cortex for touch), polysensory and more complex cognits will be
distributed more broadly, in higher association cortical regions.
At the highest level, in the upper reaches of the posterior cortex, that is, in
the broad confluence of the occipital, parietal, and temporal regions, lie dis-
tributed the most general and abstract cognits, the semantic memories and
knowledge of facts and concepts that derive from sensory experience.
Because such memories and knowledge derive from multiple experiences,
and are largely generalizations of those experiences, their networks are the
most widely distributed, with multiple associative anchors in cognits below.
In global functional terms, therefore, cognits of ever-higher rank and gener-
ality develop from the bottom up mainly in divergent—though also to some
extent convergent—fashion. (Fuster, 2006, p. 129)
VMPFC AI DLPFC
Notably, there is recent evidence suggesting that the “instances” or “event files”
themselves may involve representations at multiple levels of specificity, not only for
stimuli, or responses, but for their associations with one another, and that matches
or “partial matches” of stimuli, responses, or of stimulus-response relations may
both facilitate, or impede, performance depending on circumstances (e.g., Horner &
Henson, 2009; Waszak, Hommel, & Allport, 2003; Race, Badre, & Wagner, 2010). For
example, responses may be transferred at the level of the motor output (e.g., the
specific finger used, such as a left key press), or the comparatively abstract meaning
of the key press (e.g., an affirmative or “yes” response vs. a negative or “no” response),
or at the level of the particular semantic or other classification judgment involved
(e.g., “larger” vs. “smaller”). Additionally, in work from our lab (Denkinger & Koutstaal,
2009) we have shown that the binding of responses (e.g., “yes”) to stimuli may trans-
fer both across different exemplars of an object (e.g., different pictures of umbrellas
or cats), suggesting some degree of abstraction with regard to the stimulus represen-
tation, and also across different and uncorrelated semantic judgments (e.g., deciding
if the object contains metal, and then, later, in a different block of trials, if the same
object, or a categorically related object, is associated with a particular sound). After
only one exposure to a stimulus, we observed significant positive facilitation
(positive priming) across a change in exemplar and a change in task—provided that
the same response (e.g., “yes”) was required for both presentations. In contrast, this
facilitation was eliminated when the response differed (“yes,” then “no,” or vice versa),
again even though the semantic classifications were not related to one another, and
occurred in separate blocks of trials. In broad terms, these and related findings
(e.g., Waszak et al., 2003) suggest that there is parallel encoding of details of stimuli,
responses, and their associations, at multiple levels of representational specificity,
and across multiple domains of perception, cognition, and action. (The event-file
account is briefly discussed in Chapter 8, at the beginning of the section on “Task
Switching.”)
In the ACT-R account, there are two sorts of long-term memory: declarative
memory, which stores facts and experiences, and is basically passive, and procedural
memory or skilled knowledge. Procedural or skilled knowledge is represented in the
form of productions—that is, knowledge structures involving “if-then” or “condition-
action” pairs that map goals, the results of memory retrieval, and perceptual input
onto actions. Productions can also combine, such that any two productions that are
used in sequence may themselves be conjoined (compiled) into a new production.
Although ACT-R was initially developed to account for “higher level cognition,” an
exclusive focus on cognition without also considering action and perception has been
increasingly recognized as both detrimental and undesirable. As stated succinctly by
Anderson and colleagues, such a “division of labor”
stimulate a code for an action directly (e.g., responding by moving the hand to the
left), without the need for memory retrieval.8
Each of these accounts thus attempts to accommodate aspects of detailed ongoing
perceptual input from the world and aspects of motor processing, and incorporates
multiple changing levels of specificity and multiple levels of control. Fuzzy trace theory
similarly emphasizes our ongoing reliance on varying levels of mental representa-
tions—and particularly underscores our predilection to use representations that are
less specific.
Fuzzy trace theory is a dual-process account of cognition that was initially largely
developed in response to puzzling observations in several related domains of investi-
gation—each of which involved considerations of the level of specificity of the repre-
sentations that individuals appeared to use in different sorts of reasoning and memory
tasks. One such observation concerned the performance of children on various rea-
soning tasks, including transitive inference, class inclusion, and probability judgment,
in relation to the children’s memory for the information presented in the problems.
The surprising outcome was that there was essentially no benefit from knowing
whether the children were able to accurately remember the details of the problem (say,
for a transitive inference problem, to remember that the “red stick is longer than the
white stick” and “the white stick is longer than the blue stick”) and being able to pre-
dict whether they answered the reasoning problem correctly (i.e., correctly inferring
the relation between two nonadjacent items, such as whether the red or blue stick is
longer). In what has come to be termed the “memory-independence effect,” it was
found that the conditional probability that a child would answer the reasoning
problem correctly, given that he or she had remembered the problem details correctly,
was essentially no different than the unconditional probability (with memory
accuracy never taken into account). To account for this surprising finding, which was
subsequently replicated in several studies, Brainerd and Kingma (1984, p. 334) pro-
posed that the children encoded “degraded, schematic representations about the
series as a whole as well as precise representations of particular relationships.”9 These
“fuzzy traces” were proposed to “contain simplified information about the overall ‘pat-
tern’ of the series rather than precise information about specific relationships,” such
as, for the sticks problem presented earlier, “things get bigger to the right.”
Additional research suggested that similar processes might also explain the perfor-
mance of adults on various reasoning tasks. Reyna and Brainerd (1991) proposed that
apparently paradoxical effects in probability judgments, such as the failure to take
into account the ratio between targets and nontargets, could likewise be explained by
individuals’ reliance on different sorts of representations, of differing levels of speci-
ficity, regarding the problem at hand, and by assuming that processing was (in some
cases) nonquantitative. They proposed not only that “reasoners encode representa-
tions at varying levels of precision” and that “those representations can be ordered
with respect to precision” but also that “reasoning gravitates to the lowest, least
precise, level in this ‘hierarchy of gist’ ” (Reyna & Brainerd, 1995, p. 10) that the
response requirements of the task will allow. In the case of numerical problems, for
example, the most precise representations might involve “ratio” representations,
whereas less precise representations might involve only “ordinal” information that
captures relative magnitude, and even less precise representations might capture only
40 THE AGILE MIND
Given that we encode both verbatim and gist information, we can, if circumstances
require, focus on either or both. For example, when looking at a line graph showing a
clear upward trend with time, we can extract the gist that “X is increasing.” However,
we can also compensate for this impression if, when we direct our attention to the
values shown on the Y-axis, we see that the actual numerical increases are very small
(and perhaps, depending on the measure involved, not at all “meaningful”), leading to
a “bottom-line” conclusion that the variable is remaining largely constant across the
time period considered. On the other hand, if circumstances are such that they require
verbatim and precise calculation, such that the solution is valid only if the correct
operations are performed, in the correct order, and the precise values of the problem
are accurately combined (for example, in mathematical calculations) then that also is
often (within capacity and other limits) possible. As suggested by the iCASA frame-
work, the “optimal” level of specificity for viewing and construing a problem or situa-
tion cannot be unilaterally dictated in advance, but rather depends on the particular
problem and the problem constraints at hand. “Optimal” performance will sometimes
require reliance on representations at greater or lesser degrees of abstraction and
precision, and often making progress in difficult multidimensional problems may
require multiple levels of representational specificity at different times.
the wide range of territory considered, the number of cases with just cause for offense
is likely to be high. In general, consistent with the broadly integrative aims of the
iCASA framework, I have chosen to highlight wider and more diverse forms of
evidence relating to agile thinking than would typically be considered under the vari-
ous related but generally more specific concepts differentiated earlier (e.g., executive
or self-regulatory control, or creativity), on the basis that readers could refer to
extended treatments of those topics elsewhere. With regard to types of sources of
evidence, I have in the majority of cases, though not always, opted to emphasize
empirical research articles, rather than monographs, or book chapters, assuming that
journal articles are also likely to be more broadly and easily accessed by others.
Three further points. First, there is no individual chapter explicitly devoted to the
topic of “attention,” because attention is an integral part of movements between both
levels of control and levels of specificity, and thus considerations of attention are
relevant throughout the chapters. Second, there are few explicit references to genetic or
behavioral genetic contributions, in part because relevant research in these areas
remains in a state of dynamic flux, but more directly due to my lack of expertise in this
domain. Third, although the notion of “mental representations” itself has invited
extensive critical dialog both within cognitive science and philosophy, the grounds for
assuming mental representations are not explicitly defended here, though in several
places our ongoing reliance on objects and also actions in the world to support
knowledge, memory, and thinking (epistemic objects and actions) are underscored.
particulars, and the second relating to something that the American writer Sherwood
Anderson said with respect to the writing of Gertrude Stein, who had earlier been at
the Psychological Laboratory at Harvard University, and, together with Leon Solomons,
had completed experiments on “automatic writing.”11
PA R T I I
The chapters in Part II—Chapters 5, 6, and 7—all broaden our scope to explore more
fully additional aspects of the “entire person” as potential sources of both flexibility
and rigidity of thinking. The focus of these three chapters is, respectively, action
and motivation, emotion and aspects of the self and personality, and “higher order”
Ag il ity of Mind and t h e iC ASA F ram e w ork 45
flexible thinking is both directly and indirectly underscored. Several different domains
are considered beginning, for example, with the effects of our beliefs about knowledge,
learning, and memory on thinking, and also including aspects relating to temperament
and emotion (e.g., intolerance of uncertainty; optimism vs. pessimism); and motiva-
tion. We here also focus on those desirable forms of spontaneity and comparatively
“effortless attention” that we experience during states of absorption and flow, and the
nature of the conditions—including a more concrete rather than abstract focus—
that are conducive to what has been dubbed as “hypoegoic self-regulation.” Evidence
relating to some of the potential beneficial contributions of unconscious processing to
agile thinking is then critically assessed, focusing on theoretical and methodological
factors relevant to evaluating the effects of “unconscious processing” on the quality of
decisions and judgments. This section is followed by a depiction of some of the con-
crete dynamic interactions between person and environment in shaping and pursuing
higher versus lower level goals or subgoals, and “opportunistic divergences” that may
occur during a complex multistep reasoning task. The chapter closes with a brief
consideration of the complex roles of diversity of membership in the groups and
organizations to which we belong in shaping creatively adaptive thinking and problem
solving.
PA R T I I I
The third and final part of the book focuses on the brain bases of agile thinking.
The first two of the four chapters in Part III (Chapters 8 and 9) are paired in that they
consider neuroimaging, neuropsychological, neurophysiological, and neurochemical
sources of evidence regarding the conditions that foster or impede agility of mind,
both in terms of changing or sustaining levels of representational control and chang-
ing or sustaining levels of representational specificity. Similarly, Chapters 10 and 11
are paired, but in this case on the basis of the nature of the evidence reviewed. Chapter
10 focuses first on indirect (longitudinal, epidemiological) evidence for the role of
environmental stimulation in fostering and maintaining cognitive function, whereas
Chapter 11 turns to the relatively smaller but nonetheless increasingly persuasive
body of direct (experimental) evidence for a functional relation between diverse forms
of cognitive and sensory-motor stimulation and agile thinking.
Chapter 8 begins with an overview of the ways in which the frontal cortex is
uniquely situated to enable both abstraction and flexibility, and adaptability and con-
trol. The central role of neurons in prefrontal cortex in enabling the flexible and
abstract representation of categories and rules is then underscored by first, evidence
from single-cell recordings in the awake behaving (classifying and thinking!) monkey,
and second, two analytical neuroimaging studies examining the hierarchical ordering
of control processes and/or representations within the frontal cortex. Two subsequent
sections consider the neurochemical and neuroanatomical contributions to three
different forms of cognitive flexibility, including set shifting, reversal learning, and
task switching, and neuropsychological and lesion evidence regarding forms of spon-
taneous flexibility, such as fluency and divergent thinking. Lesion and neuroimaging
studies, psychopharmacological manipulations (e.g., effects on reversal learning
through manipulation of the neurotransmitter serotonin through dietary tryptophan
Ag il ity of Mind and t h e iC ASA F ram e w ork 47
depletion), and behavioral manipulations are among the sources of evidence consid-
ered. However, the necessity to go beyond an overly narrow, and too exclusive, focus
on frontal function, to consider dynamic anterior-to-posterior and across-system
interactions is then demonstrated by an in-depth treatment of two related topics.
First, our consideration of the neural correlates of fluid intelligence highlights the
central role of frontal-parietal interactions in providing the essential capability for
integration and control that is necessary for optimally recruiting internal resources in
the pursuit of goal-directed behavior in dynamically changing environments. Second,
our consideration of the multiple neural systems that enable working memory, includ-
ing not only prefrontal control systems but also parietal attentional systems, poste-
rior high-level and low-level perceptual systems, and medial-temporal binding
systems, further underscores the highly dynamic anterior-to-posterior and across-
system interactions that together subserve our ability to actively hold, manipulate,
and update the information we “have in mind” as we seek to accomplish our goals and
concurrently continuously encounter new information.
Chapter 9 turns to look at the brain bases of our knowledge about concepts
(semantic cognition) and of more intuitive forms of processing such as insight
and accessing remote alternatives, as well as intersections between cognition and
emotion and motivation. The first section is closely linked to the earlier chapter,
Chapter 4, entitled “Thinking with Our Senses,” and outlines evidence relating to both
concrete and multimodal representation, and also abstract and amodal, representa-
tion in the brain. The neural bases of relational and analogical processing, and of intu-
itive processing, including partially informed guessing, gist-based predictions, and
insight are then considered. These topics lead into a section that explores the continu-
ally changing dynamic interrelations between networks and subnetworks of the brain
that are most active when we are performing a specific structured and cognitively
demanding task versus when either we do not have an explicit task to perform, or we
are performing a less-than-fully-demanding task during which various sorts of spon-
taneous cognitions emerge. This section also highlights the potential “network-
switching” role assumed by “salience” networks, briefly introduced earlier and in
Figure 1.6, with particular attention on the possible role of the anterior insula.
Explored here is the proposal that the extremely diverse and virtually omnipresent
role of the anterior insula in a very wide range of conditions involving awareness may
be based on the combination and integration of multiple forms of “saliency” maps,
such that this region may comprise a representation of the “now” that further
centrally contributes to a “sentient self.” The chapter ends with a brief treatment of
the possible neurobiological contributors to resilience in the face of stress and trauma,
followed by sections on the bases of reactive control in the behavioral activation and
behavioral inhibition systems, and functional neuroimaging evidence for not only
separate but also integrated effects of emotion and cognition on working memory and
cognitive control tasks.
Chapter 10 begins by considering demonstrations of cortical plasticity in the
face of changing sensory-motor stimulation, and evidence specifically addressed
toward establishing the functional relevance of such changes. We then consider
evidence for such plasticity provided by studies on the acquisition of specialized skills
such as spatial-navigational learning. A conceptual and empirical orientation to three
48 THE AGILE MIND
key concepts relating to brain plasticity in aging and across the life span—involving
the ideas of brain or cerebral reserve, of cognitive reserve, and of compensation—
then provides background for a consideration of longitudinal and epidemiologic
research on the longer term benefits of various sorts of environmental stimulation.
Research on environmental stimulation is somewhat artificially separated into treat-
ments relating to the effects of education, social interactions, occupational factors,
and leisure activities. Additional sections consider longitudinal evidence relating to
the potential benefits for longer term cognitive capabilities derived from second- or
multiple-language use, and physical exercise and cardiovascular fitness. A separate—
less positively focused but crucial section—then documents some of the evidence
on the substantial adverse consequences of chronic or acute stress on adaptive cogni-
tion, including the multiple forms of stress associated with poverty and deprivation.
The final section turns our attention to initial promising outcomes derived from
multidimensional interventions in the community to foster greater cognitive and
socioemotional involvement that may promote or help to preserve mental agility and
provides a bridge to the next chapter on direct experimental interventions.
Chapter 11 first explores the extensive experimental work on “environmental
enrichment” with nonhuman animals, which has been fundamental in establishing
causal connections between stimulating environments, behavioral flexibility, and
corresponding brain changes. The chapter then turns to the multiple, often highly
innovative and creative, approaches that have been adopted in the effort to examine
plasticity of brain function in humans, in relation to experimentally assigned
sensory-motor and cognitive interventions. Included here are physical and cardiovas-
cular fitness interventions, training in deliberate recollection in older individuals
and of working memory in younger and older adults, and training of attention in
young children. Two additional sections consider the benefits for flexible cognition
that may be derived from, on the one hand, playing certain forms of real-time
video games and, on the other hand, certain forms of experiences with the
natural environment. An experimental intervention with older individuals based
on multimodal engagement in novel activities designed to invite playful and imagina-
tive participation points toward further promising approaches. This chapter also
considers a recent speculative theoretical proposal regarding the linkages between
stimulating physical activity and the generation of new neurons (neurogenesis),
particularly in the hippocampal dentate gyrus. Here I also suggest that, broadly speak-
ing, diverse forms of cognitive and other stimulation may be seen as extending
our “exemplar space” of objects, events, people, qualities, and so on, thereby increas-
ing the range of instances and sets of instances that we can draw upon in thinking,
reasoning, and acting.
Chapter 12 is the final chapter and is organized in the form of broad questions that
are then expanded by selected reminders of key findings, additional evidence regard-
ing possible applications or implications, and more specific questions and research
directions. The questions are very broadly grouped into four sections, concerning
(a) oscillatory range in levels of specificity and levels of control, (b) environmental
enrichment and stimulation, (c) the interpenetration of concepts with perception,
action/motivation, and emotion, and (d) broader educational, policy, and ethical
implications.
Ag il ity of Mind and t h e iC ASA F ram e w ork 49
In this passage, William James offers us a powerful image of the twin necessity of
“abstract concepts” and “perceptual particulars” in flexibly adaptive thought. Lacking
abstract concepts, we could, nonetheless, move about in the world, but our movement
would be that of the slightly awkward, tentative, and never entirely stable hopping of
a person newly restricted to the use of one leg. Or (shamelessly changing metaphors),
we would be like slow waders, moving laboriously against the heavy deeps of an
endless sea and downpour of particulars that assail us from all sides. Elsewhere James
elaborated on the advantages of concepts in dealing with the endless flux and variety
of particulars:
With the help of both abstraction and particularity—using concepts along with the
particulars—we have the wherewithal to move with greater power and also wider
vision, in an iterative bootstrapping (a recurrent anchoring and forward motion) of
concept to percept, percept to concept, concept to percept. With our concepts, formed
from and based upon our past experiences with other instances of a given sort, we
anticipate (predict) what is most likely to ensue from our actions and choices. Then we
50 THE AGILE MIND
take note of (observe, evaluate) the particular consequences that did, in fact, arise in
the world as a result of that action or choice, reimmersing ourselves in the particular
particulars of the world. But we do not remain there. Instead, newly versed in
particulars, we move back again to our concepts, and to new anticipations and new
predictions, the actual outcomes of which are in turn again evaluated as particulars, in
an ever-interchanging movement, up-down, up-down, flexibly and fluidly across
and within the thick of experience.
In agreement with William James, a prominent and recurrent theme of this
book is that the movement between levels of specificity—abstract to particular—
is a crucial contributor to flexibly adaptive thought, and to agile minds. But the
abstract-specific dimension concerns the “what” of thought—the representational
content of thought, rather than the processes by which thought occurs. What about the
manner of thinking—the way of thinking, rather than the what?
The processes of agile thought also involve an ever-interchanging movement,
but with extremes or end points of a different sort. Adaptive thought requires move-
ment between highly controlled (deliberate, intentional, goal-guided, systematic)
thinking, and less controlled or automatic (nondeliberate, nonintentional, habit-
guided, intuitive) thinking, and often occurs in a broad, not sufficiently understood
intermediate zone, near and straddling the center point, that involves spontaneous
fluidity, improvisation, and creative “practice beyond the rules.” This intermediate zone,
and movements within and across it, from relatively more controlled to relatively
more automatic phases, of sometimes longer, sometimes shorter durations, is
succinctly and powerfully pointed to by the second quotation, offered by Sherwood
Anderson in his defense of Gertrude Stein:
It is, and it isn’t. All good writing (and also other good kinds of thinking and
making) is neither exclusively automatic, nor exclusively nonautomatic.
This is the second prominent theme of this book that closely intersects with the
first theme. We frequently have the capacity to respond to situations and information
in different ways: highly controlled, intentional, effortful, and deliberate on the one
side, versus less controlled, more automatic, with little effort or explicit deliberation
on the other side. These two functional-behavioral extremes—together with an inter-
mediate zone characterized by relatively greater spontaneity and improvisation and
increased receptive attention—provide complementary advantages and disadvan-
tages, and so they may supplement and compensate for specific weaknesses in either
extreme alone.
Part One
MEMORY, CATEGORIZATION,
AND CONCEPTS
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2
Flexibly Using Memory and
Categorical Knowledge, Part 1
Levels of Representational Specificity and Thinking
53
54 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
us to transfer what we have learned to new contexts that “echo” or “mirror” the past
only partially and in some rather than all respects. More abstract, categorical,
or gist-based retention also is crucial to many complex and adaptively significant
forms of thought such as creating and understanding analogies and metaphors, and
drawing inferences based on the classification of events and objects.
Thus, this chapter argues that agile thinking requires the retention and use of
both specific and abstract memory and knowledge—and the ability to flexibly and
adaptively move between them as needed. The research evidence leading to this
conclusion is diverse, and it includes empirical findings from a number of areas of
psychology that are not “standard fare” in treatments of creativity or thinking and
problem solving, such as case studies of superior memory, and theoretical consider-
ations of the nature of the cognitive and affective information processes that contri-
bute to impaired thinking and problem solving in conditions such as clinical depression
and chronic worry. Rather than beginning with a consideration of the results from
prototypical cognitive psychology experiments, this chapter will begin with these
more “peripheral” findings, moving toward central studies. We will first consider the
hazards of an overly extreme form of memory at either end of the specific-to-abstract
continuum—either predominantly, and too consistently, specific or predominantly
too categorical and abstract. Then we will consider several converging sources of
evidence supporting the importance of movement between levels of specificity in
enabling adaptive thinking.
As will be seen, particular conditions that involve changes in an individual’s
capacity to flexibly access mental representations at differing levels of specificity,
such as memory and information processing in clinical depression or normal
aging, frequently also involve disruptions in aspects of intentional control (control vs.
automaticity). Nonetheless, conceptual and empirical clarity will be enhanced
if we initially consider these two dimensions and their relation to the iCASA
(integrated Controlled-Automatic, Specific-Abstract) framework separately. This
chapter focuses on factors that shape flexible thinking that predominantly involve
the content of representations, relating to where representations fall on the level of
specificity continuum from abstract to specific. The following (companion) chapter
focuses on levels of representation as contributing to flexible thinking predominantly
from the perspective of representational process with regard to the controlled-automatic
distinction.
in an e-mail to memory researchers James McGaugh and Larry Cahill. In that e-mail
she wrote:
… since I was eleven I have had this unbelievable ability to recall my past.
[…] Whenever I see a date flash on the television (or anywhere else for that
matter) I automatically go back to that day and remember where I was, what
I was doing, what day it fell on, and on and on and on. It is non-stop, uncon-
trollable and totally exhausting. […] Most have called it a gift, but I call it a
burden. (Parker et al., 2006, p. 35)
Extensive testing demonstrated that what AJ then first reported of her own
memory abilities is, indeed, true. She has remarkably detailed and specific memory for
her own personal experiences, particularly those after the age of 13 and also for world
events that have become associated with her experiences. She has extremely vivid
autobiographical memories, filled with emotion, that come to her automatically,
without her conscious control. When, without warning, she was given a date such as
“July 1, 1986” or “April 3, 1980,” AJ promptly and with little effort, related where she
was that day, the day of the week it was, what she was doing, and the people she was
with. She also remembers world events that occurred on the day, such as political
events, and natural or human disasters. Her recollections are very reliable. Asked on
different occasions about a given date, her answers are highly consistent with one
another, and cross-checking between the diary entries that she has made and her
reported recollections likewise reveal incredible accuracy. Not surprisingly, AJ spends
a great deal of her time remembering and talking about her memories, and, as we saw,
describes her memory as “nonstop, uncontrollable, and automatic.”
But, despite her vivid and detailed autobiographical memory, AJ does not perform
well on all tests of recently learned material. For instance, although she performed
perfectly, or almost perfectly, not only on tests of autobiographical memory but also
on tests of word recognition and a test of memory for new associations (visual paired
associates between shapes and colors), her recall of semantically related lists of words
(16 words belonging to the four semantic categories of fruits, tools, spices, and clothing)
was significantly below normal, as also was her ability to recall a complex novel visual
figure after a delay. The latter two memory tasks rely heavily on a person’s ability to
organize material, by grouping items together based on their categorical similarity
(e.g., grouping together all of the clothing items on the to-be-remembered word list)
or by identifying more global versus local structural patterns in a complex line draw-
ing. AJ’s difficulties in performing these tasks suggest that she may have difficulties in
abstracting out commonalities or overall structure in newly learned information.
Consistent with this possibility, AJ showed marked deficits on tasks requiring the
abstraction of rules or principles. For instance, she was impaired at attempts to flexi-
bly determine the categorical basis or “rule” that another person was using to sort
stimuli that differed on a number of dimensions (e.g., in color, shape, and number).
She showed a high level of repetitive (perseverative) errors on this task—the Wisconsin
Card Sorting Task—reflecting a tendency to “get stuck” in using a category rule that,
although once correct, was no longer correct (38 perseverative responses, correspond-
ing to an error rate that was nearly 2 standard deviations higher than average).
56 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
She also had considerable difficulty performing another widely used neuropsycho-
logical test of abstraction and concept formation (the Halstead Category Test) that
similarly requires both concept formation and the ability to flexibly shift one’s mental
set. She made 78 errors on this test, obtaining a total correct score that was 2.3
standard deviations below the average for the test—a remarkably low score particu-
larly in the context of her intact, or even superior, scores on several other tests.
Tasks involving analogical reasoning likewise posed a challenge for AJ. Her score on
the Similarities subtest from the Wechsler Adult Intelligence Scale-Revised, in which a
person is shown pairs of apparently dissimilar words and asked to say how the words
in each pair are related, was more than 1.5 standard deviations below average
(Z = –1.67). AJ’s answers to the similarities problems also showed a strong tendency
toward concrete rather than abstract answers.
These patterns of deficits, involving weaknesses in analogical reasoning and
a tendency toward excessive concreteness, are surprisingly consistent with deficits
that have been noted in some other individuals with “super-normal” memory. For
instance, in his descriptions of case “S,” another individual with superior memory, the
neuropsychologist Alexander Luria (1968) observed that, despite his outstanding
ability to remember recently encountered materials, S was viewed by others as disor-
ganized and not very bright, and he often had trouble with abstraction. S himself was
acutely aware of his proclivity for becoming side-tracked in detailed sensory associa-
tions and memories. Such side-tracking arose both as a consequence of his vivid imag-
ery abilities and as a result of S’s synaesthesia: that is, an involuntary conjoining of
information from one physically experienced sense modality (e.g., color) with infor-
mation in another sensory modality that is subjectively experienced as also real
(e.g., sound), but that emerges from within the individual’s own sensory-perceptual
mental representations (e.g., Ramachandran & Hubbard, 2001; J. Ward et al., 2008;
see also A. L. Murray, 2010 and Simner et al., 2009). S’s synaesthesia often involved
colors and tastes, as well as sounds. In combination, the imagery and synaesthesia
made it difficult for him to extract and follow the gist of a story or explanation:
All this makes it impossible for me to stick to the subject we’re discussing.
[…] Say you ask me about a horse. There’s also its color and taste I have to
consider. And this produces such a mass of impressions that if ‘I’ don’t get
the situation in hand, we won’t get anywhere with the discussion. […] I have
to deal not only with the word horse but with its taste, the yard it’s penned
in—which I can’t seem to get away from myself. (Luria, 1968, p. 156)
Who would expect that VP [another individual with superior memory], who
could play seven simultaneous chess games blindfolded, and had an estimated
IQ of 136, would be employed as a store clerk? […] How paradoxical that
Luria’s case S, who could recall seemingly unlimited amounts of materials for
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 57
years, had trouble capturing the meaning of what he read and moved from
one job to another, eventually becoming a professional mnemonist. (Parker
et al., 2006, p. 48)
Other individuals with superior memory similarly have been reported to have
difficulty with forms of abstraction. TM, a man with a remarkable memory studied by
Wilding and Valentine, showed pronounced difficulty recalling a complex story that
required “constant inference and interpretation” (Wilding & Valentine, 1994, p. 508).
Anecdotal comments from TM’s friends suggested that “he sometimes had problems
understanding social conventions which are transparently obvious to most adults, due
to his tendency to concentrate on physical aspects of events rather than meanings”
(p. 508).1 Similarly, the savant Kim Peek has an astonishing ability to remember text
(and also music) verbatim; to date, he has learned approximately 9,000 books “by heart”
on a diverse range of topics. In contrast with many savants, he does understand much
of what he remembers, and he has also increasingly moved from rote memory into a
form of associative, and sometimes creative, thought. Nonetheless, he has a limited
capacity for abstract, conceptual thinking. For instance, he cannot explain the meaning
of many commonplace proverbs, and sometimes he responds to questions in a very
concrete and literal manner (Treffert & Christensen, 2005; see also A. Snyder, 2009).
Jerome Bruner, in his foreword to the first edition of Luria’s book about S,
The Mind of a Mnemonist: A Little Book about a Vast Memory, wrote:
For the mnemonist, S, whose case is studied in such exquisite detail in these
pages, is a man whose memory is a memory of particulars, particulars that are
rich in imagery, thematic elaboration, and affect. But it is a memory that is
peculiarly lacking in one important feature: the capacity to convert encounters
with the particular into instances of the general, enabling one to form general
concepts even though the particulars are lost. (Bruner, in Luria, 1968, p. xxii)
The strikingly simple but important message is clear enough. Although highly
specific memory is critical in many contexts in which the precise retention and retrieval
of information is essential, on its own, and when present to the exclusion of more
abstract or gist-based memory and categorization, it can impede the flexible adaptive
use of information in less literal, less narrowly reduplicative ways.2 Beyond remember-
ing the details, we also need to understand the general gist of our experiences, and we
need to be able to identify patterns and parallels between different events or ideas at
the level of general principles and deeper, more abstract similarities.
Possible Mechanisms
Here we will focus on the more recent and, to date, apparently unique case of AJ,
involving AJ’s supra-normal retention and recall of information from her personal
past. Parker and colleagues (2006) suggested that this condition might be termed
“hyperthymestic syndrome” involving two defining features. First, the individual
devotes an unusually large proportion of time to thinking about his or her personal
58 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
past, and second, the individual has “an extraordinary capacity” to recall specific
events from his or her personal past. Based on the neuropsychological findings pre-
sented earlier, a clear candidate cognitive mechanism that may contribute to this
syndrome includes deficits in executive functions, particularly those involving
abstraction, self-generated organization, and mental control. However, besides impair-
ments in abstraction, AJ also showed a pattern of problems in naming objects that
might reflect deficits in anterior left hemisphere function. On the Boston Naming
Test (Lezak, 1995), a test that requires the individual to name pictures (line drawings)
of objects, AJ demonstrated a tendency to provide incorrect names, such as calling
dominoes “dice,” a palette “paint,” and an abacus, “Chinese checkers,” leading her to
obtain a naming score that was 2.7 standard deviations below average. AJ also some-
times shows difficulty producing appropriately precise terms in spontaneous speech.
The full neuropsychological assessment also yielded some evidence of atypical brain
lateralization. Although a standard questionnaire measure of handedness indicated
that she is entirely right-handed or “right dominant,” a photograph of her at 35
months of age showed her using her left hand, and she worked right to left on several
different tasks, such as the complex figure task. Her “mental calendars” also go from
the right to the left. Additionally, AJ showed impairments in face recognition (with
intact face perception), and a self-reported long-standing abnormal insistence on
order in her external environment: She refers to herself as a “neat freak” and, as a
child, would keep her toys in a “very precise and complicated order” becoming
distraught if things were moved—reflecting obsessive-compulsive tendencies.
On the basis of these combined neuropsychological and cognitive performance
assessments, Parker and colleagues (2006) propose that AJ may have a variant of a
neurodevelopmental frontostriatal disorder. (See Simner et al., 2009, for an alterna-
tive account, emphasizing that the combination of AJ’s time-space synaesthesia and
her obsessive tendencies may have led to her savant-like autobiographical memory
abilities.)3 This complex group of neurodevelopmental disorders also includes condi-
tions such as autism, obsessive-compulsive disorder, attention-deficit/hyperactivity
disorder, Tourette’s syndrome, depression, and schizophrenia. A commonality across
these disorders is that they all involve impairments in executive functioning as
a consequence of impairments to the frontostriatal system. This system includes
regions of the frontal cortex (dorsolateral prefrontal and lateral orbitofrontal cortex),
anterior cingulate, the supplementary motor area, and associated deep brain basal-
ganglia structures, including the caudate, putamen, and globus pallidus (Bradshaw &
Sheppard, 2000; Chudasama & Robbins, 2006). Stated both broadly and succinctly,
the frontostriatal system is “responsible for our adaptive responses (initiation,
execution, or withholding) to environmental situations” (Bradshaw & Sheppard, 2000,
p. 297; for recent review, see Kehagia, Murray & Robbins, 2010).
A schematic diagram, illustrating the role of the prefrontal cortex—with connec-
tions to the basal ganglia,4 and also sensory cortex and motor cortex—in flexibly
adaptive cognitive control is provided in Figure 2.1. In the figure, interactions between
the prefrontal cortex (PFC) and the basal ganglia are shown as basal ganglia loops
(BG loops), that are influenced by reward signals involving dopamine (DA), particu-
larly with respect to learned associations between various possible contextual and
other “cues” to behavior (here designated as C1, C2, C3), such as sensory cues, current
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 59
DA reward
BG loops PFC
“Context”
C1
C2
R1
C3
“Cue” Sensory
cortex Motor R2
cortex
Active
motivational states, and memories, and also possible voluntary responses (here
designated as R1 and R2). Also shown are internal, or “hidden,” units that represent
more central stages of processing. The dark (solid) circles in the figure indicate active
units or pathways, and thick lines indicate well-established pathways that mediate
well-established (habitual or prepotent) responses.
The PFC is not heavily connected with primary sensory or motor cortices, but
instead is connected with higher-level “association” and premotor cortices.
Via interactions with the basal ganglia […], dopaminergic (DA) reward
signals foster the formation of a task model, a neural representation that
reflects the learned associations between task-relevant information (as shown
by the recursive arrow). A subset of the information (e.g., C1 and C2) can then
evoke the entire model, including information about the appropriate response
(e.g., R1). Thus, the PFC can coordinate processing throughout the brain and
steer processing away from a prepotent (reflexive) response (C3 to R2) toward
a weakly established, but more goal-relevant, response (C3 to R1). Excitatory
signals from the PFC feed back to other brain systems to enable task-relevant
neural pathways. (E. K. Miller & Buschman, 2008, p. 423)
Once a particular complex rule or task mapping between cues to responses has
been learned, the rule or “task model” may later be elicited in response to only a subset
60 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
of the original cues (e.g., here, the cues of only C1 and C3 may elicit the appropriate
response of R1). Frontal-striatal interactions of this form may thereby “coordinate
processing throughout the brain and steer processing away from a prepotent (reflex-
ive) response [. . .] toward a more weakly established but more goal-relevant, response”
(E. K. Miller & Buschman, 2008, p. 423). This is here illustrated in the strong connec-
tions (dark thick lines) between C3 and R2, yet, despite this prepotent response,
this strong response is not made: Note that R2 is not indicated as active, whereas
R1 is, together with the connections between R1 and sensory and motor association
cortex and representations in prefrontal cortex. The frontostriatal system is, there-
fore, a central contributor to adaptive and flexible thinking.
O V E R R E L I A N C E O N A B S T R A C T C AT E G O R Y I N F O R M AT I O N
IN CLINICAL DEPRESSION
Some individuals with depression show a marked increase in the recall of very general
memories concerning their personal past and a decrease in more specific autobio-
graphical memories. These reductions in the specificity of memory retrieval for
personal events are, in turn, associated with reduced effectiveness and flexibility in
problem solving. When asked to recall events from their life in response to particular
cue words or probes (e.g., surprised, happy, sorry, angry), individuals who are depressed
often provide categorical memories such as (in response to the cue “happy”), “when I
go dancing” or (in response to the cue, “leisure”), “playing squash on Mondays.” These
are memories that refer to a repeated class or general type of event, and to something
that has happened several or many times, rather than to a single specific event that
occurred in a particular place and time.5
Memories of this sort fall at an intermediate level of specificity in a hierarchical
structure of autobiographical memory that has been proposed and developed by
Martin Conway (1996, 2005, Conway & Pleydell-Pearce, 2000; see also Conway, 2009).
The model is schematically shown in Figure 2.2. As can be seen in the figure, according
to this hierarchical view of our self-related memories, there are several broad types
of memories, at differing levels of abstraction versus specificity. At the top of the
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 61
Life story
Themes
Relationship
Work theme
theme
Lifetime
periods
The Working at Friends with
conceptual University X: ‘Y’
self
Others Others
Activities Activities
Locations Locations
Projects Projects
General Goals Goals
events
Prof.
Smith
Psych.
Dept. Dept.
talks
Grant
‘Z’
Promotion
Episodic
memories
hierarchy are very broad and abstract or overarching themes, such as our overall “life
story,” or themes relating to our work and relationships. Connected to these themes
are somewhat more specific groups of memories, concerning phases of our lives or
lifetime periods and also general events. Each of these general events is, in turn, con-
nected to several more specific occurrences or episodes (“episodic memories”),
62 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
involving knowledge about particular events that we have experienced, with such
details as exactly where and when and how something happened, or how we felt, or
particular sensory-perceptual details, and so on.
The categories of repeated life events that individuals with depression tend to recall
are of the “general event” sort. These memories are less closely anchored to concrete
sensory-perceptual and other details than are memories of individual, temporally and
spatially unique events (episodic memories or “event-specific knowledge”). Such
memories are, however, more specific than knowledge about extended “lifetime
periods” that involve longer phases of an individual’s life history.
Evidence that individuals experiencing a major depressive episode show an
enhanced rate of overgeneral (categorical) autobiographical memory retrieval has
been provided by a large number of studies. A meta-analysis by J. M. G. Williams and
colleagues (2007; also see van Vreeswijk & de Wilde, 2004) reported an average
effect size (Cohen’s d) of 1.12 across 11 studies of depressed patients versus controls;
that is, on average, the mean level of overgeneral categorical memories in depressed
individuals was 1.12 standard deviations higher than that provided by individuals in
the control conditions. Besides major depression, overgeneral autobiographical
memory retrieval has been observed in several other related affective disorders, such
as postnatal depression, manic-depressive disorder, and in individuals who are
dysphoric but who do not meet clinical criteria for major depression (average effect
size d of 0.94 across a total of 28 studies; Williams et al., 2007). Two other, often
related, conditions that have been associated with overgeneral memory are a history
of trauma or abuse, and suicidality. Indeed, the first instances of reported overgeneral
memory arose in the context of studying suicidal patients (J. M. G. Williams &
Broadbent, 1986), and several subsequent studies have likewise reported increased
overgenerality of autobiographical memory in suicidal compared with nonsuicidal
individuals (J. Evans et al., 1992; Pollock & Williams, 2001; J. M. G. Williams &
Dritschel, 1988; J. M. G. Williams, Ellis, et al., 1996).
The observation of overly general autobiographical memory retrieval in these con-
ditions shows some generality across different methods that can be used to prompt, or
cue, the retrieval of self-related memories. Although autobiographical memory over-
generality is most frequently reported for memory prompts involving single words,
and typically emotion words, such as “happy” or “angry,” overgeneral memory also has
been found when the recall prompts were brief descriptions of scenarios that were
emotionally positive or emotionally negative. When the cues concerned the provision
of reassurance or help, or the occurrence of criticism or difficulties, in relation to a
partner, friend, sibling, or neighbor (e.g., “Recall a time when a neighbor helped you
with a practical problem,” R. G. Moore et al., 1988), depressed individuals produced
twice as many categorical memories in response to these sentence cue prompts than
did nondepressed age-matched controls. Consistent with both earlier and subsequent
studies, these findings suggest that “the cognition of depressed people is likely to be
dominated by relatively abstract representations of the past rather than specific
instances” (R. G. Moore et al., 1988, p. 276). Increased overgeneral memory also has
been observed in individuals with posttraumatic stress disorder (PTSD; relative to
trauma survivors without PTSD) in response to emotional pictorial stimuli that were
thematically unrelated to the traumatic events (Schönfeld & Ehlers, 2006).
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 63
Dickson & Bates, 2006; J. M. G., Williams et al., 1996; cf. Suddendorf & Corballis,
1997, 2007). As will be seen in Chapter 9, there is considerable commonality in the
brain regions that are activated during thinking of (“re-experiencing”) the past and
imagining (“pre-experiencing”) the future (e.g., Addis, Wong, & Schacter, 2007;
Schacter & Addis, 2007a); furthermore, in various populations, deficits in the retrieval
of specific details from the past have been found to be associated with a similar
sparseness of detail in relation to the hypothetical construction of future events
(see Rosenbaum et al., 2009, and Buckner, 2010, for recent review and discussion).
One proposed explanation of the observed impairments in problem solving is that
depressed individuals are drawing on a reduced fund of particular world experiences due
to impairments in autobiographical memory. The ability to recall related past events
that are highly detailed and elaborated might provide a strong “case-based” database
that could aid in cuing new ideas or alternative approaches that could be used to
address the current difficulty: “In a problem-solving situation specific memories can
function as a rich and detailed database offering a large number of cues from which to
develop potential solutions” (Pollock & Williams, 2001, p. 387). However, given that
depression also is associated with an increased likelihood of engaging in rumination,
involving repetitive, largely linguistic, passive thinking about one’s symptoms of
depression, and the possible causes and consequences of those symptoms (Nolen-
Hoeksema, 1991; Nolen-Hoeksema et al., 2008), an alternative account is that the
impairments in problem solving arise because of increased rumination.
As will be seen later, rumination does seem to play an important role in maintain-
ing and exacerbating impaired problem solving of depressed individuals (e.g., Watkins
& Baracaia, 2002; see Watkins, 2008, for broad conceptual review). Yet it does not
appear that this factor, on its own, provides an entirely sufficient account. Raes and
colleagues (2005) found that overgeneral memory was itself an important contributor
to the deficits in problem solving, rather than only a covarying factor of rumination.
More cogently, experimental manipulations of the level of retrieval specificity
suggest that overgeneral memory retrieval is an important determinant of the
decrements in problem-solving performance. In one experiment (J. M. G. Williams
et al., 2006, Expt. 5), nondepressed students were assigned to one of two groups,
in which they were directly encouraged to retrieve either specific events (that is,
“an event that lasted less than a day and occurred at a particular time and place”) or
categorical events (here, participants were asked to write a description of the type of
event that the cue reminded them of, that is, “the sort of event that happens or
has happened in the past”). As expected, the two randomly assigned groups of nonde-
pressed students did not differ in problem-solving performance on an initial
pretest measure. However, individuals who received the generic memory induction
instructions showed a significant decline in performance from pre- to posttest,
whereas those completing the specific induction showed no change in problem-
solving performance (Williams et al., 2006, Expt. 5).
Another experiment used a more indirect method to elicit either specific event or
categorical event retrieval, and likewise demonstrated beneficial effects on problem
solving arising from more specific retrieval. This experiment (Williams et al., 2006,
Expt. 4) involved a manipulation of the imageability of the retrieval cue words, using
either words that were associated with low levels of imagery, and are known to elicit
primarily more general memories (J. M. G. Williams, Healy, & Ellis, 1999), or words
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 65
that evoked high levels of imagery. Mirroring the effects obtained with the more direct
manipulation of participants’ level of specificity of event retrieval, cue words that were
low in imageability led to reductions in successful problem solving compared with cue
words that were high in imageability. Although the two groups did not differ in the
number of relevant methods (means) that they suggested to the problems, the indi-
viduals given the high imageable cues provided significantly more specific solutions than
were provided by participants given the low imageable cues. Additionally, the proposed
solutions offered by the high imageability group were independently rated as signifi-
cantly more effective than those proposed by individuals given the low imagery cues.
Further experimental evidence directly pointing to the causal role of the level of
specificity of memory retrieval in the deficits in problem solving that are shown by
individuals with depression is provided by a study that explicitly manipulated whether
depressed and nondepressed control participants engaged in an “abstract self-focus”
versus “concrete self-focus” before they were asked to engage in a problem-solving
task. Adopting a manipulation involving ruminative focus that had been used in
earlier research (Nolen-Hoeksema & Morrow, 1993; Watkins & Teasdale, 2001, 2004),
Watkins and Moulds (2005) asked participants to work at their own pace through a list
of 28 items, each of which focused the individual’s attention on her or his self and
depressive symptoms, such as “the physical sensations in your body.” However, whereas
participants in the concrete self-focus condition were asked to use their imagination
and concentration to focus their mind on how each symptom was actually experienced,
participants in the abstract self-focus condition were encouraged to think more
abstractly about the causes, meanings, and consequences of the symptoms.
For individuals who were depressed, the concrete self-focus led to significantly more
concrete problem descriptions on the Means-Ends problem-solving task than did the
abstract self-focus. Compared with the abstract self-focus, the concrete self-focus also
led to significantly improved social problem solving, both as assessed by the number of
means provided and by ratings of the effectiveness of those suggested means. In con-
trast, looking at measures of mood, compared to initial measures, the self-focus manip-
ulation led to an increase in negative mood for both depressed patient groups (thus
replicating known detrimental effects of self-focus on mood in depressed persons);
equally important, this increase in negative mood was equivalent for the two depressed
groups. For control participants who were not depressed, the self-focus manipulation
had no effects on either their mood or their problem-solving performance.
These outcomes argue that it is not symptom-focus per se, but rather the tendency
to maintain an overly abstract conceptual manner of thinking and recollection that
impedes problem solving in depression. This conclusion was further strongly sup-
ported through a formal statistical mediational analysis, using the criteria proposed
by R. M. Baron and Kenny (1986) to establish mediation effects.6 Change in the level
of concreteness of problem descriptions was a significant mediator of the effect of
mode of ruminative self-focus on problem solving. More recently, Raes, Williams, and
Hermans (2009) reported promising results in a preliminary investigation of a memory
specificity training intervention in inpatients with depression. Likewise, Watkins,
Baeyens, and Read (2009) found decreases in depressive symptoms, and increases in
concrete thinking, following a “concreteness training” intervention in individuals
with dysphoria compared to both a waiting list control group and another closely
matched control group.
66 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
Taken together, these and similar findings strongly argue, as J. M. G. Williams et al.
(2007, p. 142) conclude, that “lack of specificity in memory, however it comes about,
can play a causal role in reducing problem-solving capacity”—particularly for the
forms of complex and ill-structured problem-solving tasks such as the MEPS included
in these studies, and that are also likely to be encountered in an individual’s daily
interactions and endeavors. Notably, recent work has further shown that decreased
specificity of autobiographical memory retrieval predicted the generation of fewer
relevant means on this complex social task also for older and younger adults who
were not depressed (Beaman et al., 2007).
Nonetheless, while the evidence does argue for a causal role of overgeneral,
categorical memory retrieval in the thinking deficits that are observed, as noted
earlier, such overgeneral retrieval is not necessarily the only contributor. Other
factors, such as increased rumination and decreased cognitive executive resources,
might also play an important role in leading to both the increased likelihood of
overgeneral memories and reduced problem-solving capacity in depression. On the
whole, the evidence also points to these factors as assuming a contributory role in the
complex interactions that lead to the deficits. Based on their extensive review of find-
ings, J. M. G. Williams et al. (2007) propose that the diverse aspects and correlates of
overly general autobiographical memory retrieval might be best accounted for by a
combination of three factors: the “capture” of retrieval by abstract-conceptual (rumina-
tive) structures, reduced cognitive executive resources, and functional avoidance.
Functional avoidance is particularly important for the initial instigation of overly
general autobiographical memory retrieval. Simply stated, functional avoidance refers
to the idea that memory retrieval becomes more general because more specific retrieval
is associated with the recollection of painful and traumatic events which, in turn, leads
individuals to try to avoid such recollection both because it is painful and because it is
potentially highly disruptive to their ongoing pursuits and goals. However, the pro-
cesses involved in functional avoidance may not themselves be simple, and (though
still not well understood) they likely involve an interactive interchange between
relatively more highly controlled versus more automatic processes. On the one hand,
it has been argued that controlled processes are invoked in an individual’s efforts to
suppress or to curtail memory retrieval of traumatic events. On the other hand,
automatic processes, particularly the highly associative (and not always highly con-
trollable or predictable) nature of human memory may be partially responsible for the
need for a global curtailment rather than selective curtailment of more richly specific
memory retrieval (e.g., Brewin, 2006; Dalgleish, 2004). The associative nature of
memory is such that even initially very positive cues might become associatively
linked (at the time of retrieval) to traumatic events. Thus, to avoid unwanted retrieval
of such events, all retrieval searches may be truncated at a more abstract “intermedi-
ate” level of specificity.
The second, and for our purposes, especially important aspect of the model
proposed by Williams and colleagues, involves “capture” of retrieval by abstract-
conceptual (ruminative) structures. As noted, rumination has been defined as
passively focusing one’s attention on a negative emotional state, its symptoms, and
thinking repetitively about the causes, meanings, and consequences of that state
(Nolen-Hoeksema, 1991; Nolen-Hoeksema et al., 2008). With frequent retrieval and
elaboration, these particular modes of thinking (chronic themes or concerns) become
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 67
highly dominant and associatively linked to many other concepts. Once activated,
then, the themes tend to rapidly capture attention, inviting continued activation and
rumination in a self-perpetuating circle. This, in turn, makes it increasingly difficult to
move beyond intermediate, categorical memory descriptions of events—a state called
“mnemonic-interlock” by J. M. G. Williams (1996) or “dysfacilitation of the retrieval
process” by M. A. Conway and Pleydell-Pearce (2000).
The third and last factor in the model of Williams et al. is a deficit in cognitive
executive processes. (Note that a deficit in executive processes was also proposed in
the case of AJ, but here, rather than overly specific retrieval, it is overly abstract or
categorical memory retrieval that ensues.) Executive processes are central to all
aspects of generative memory retrieval, beginning with the initial processes of inter-
preting information or cues with regard to a retrieval goal, and continuing through the
phases of monitoring and checking any associations and memories that emerge and,
if necessary, inhibiting irrelevant associations, to finally organizing and expressing
the outcome of the search (e.g., M. A. Conway & Pleydell-Pearce, 2000; Whitten &
Leonard, 1981; D. M. Williams & Hollan, 1981).7 For example, reduced executive con-
trol was shown to be linked to overgeneral memory retrieval in an extensive series of
studies reported by Dalgleish et al. (2007), with reduced specificity in autobiographi-
cal memory associated with several tasks requiring executive control, such as verbal
fluency, block design, and fluid intelligence, and also linked with increased errors on
tasks such as design fluency and the Alternative Uses Task. The proposed interactions
between these three mechanisms—capture and rumination, functional avoidance,
and reduced executive processes—are diagrammed in Figure 2.3.
Capture &
rumination
Executive
capacity
and control
R E D U C E D C O N C R E T E N E S S O F R E P R E S E N TAT I O N S
IN CHRONIC WORRY
Although less extensively researched than is overgeneral memory in clinical
depression, there is increasing evidence that broadly similar processes may be at work
in the maintenance of chronic worry. Excessive reliance on overly abstract and verbal
representations during worrying may substantially interfere with more adaptive
problem solving with respect to precisely those issues and possibilities that are the
target of the worry.
According to the avoidance theory of worry (Borkovec, Ray, & Stöber, 1998;
see Behar et al., 2009, for conceptual overview), worry acts as a cognitive avoidance
strategy, enabling the individual to avoid confrontation with, and emotional and
cognitive processing of, a threatening situation or stimulus. This theory is grounded
in the conjunction of several findings. First, there is evidence that worry predomi-
nantly entails verbal thought, or conceptual verbal linguistic activity, unlike obsessive
intrusive thoughts, which tend to be experienced more as images. Individuals’ self-
reports suggest that worrying is composed predominantly of thoughts rather than
images (e.g., Freeston, Dugas, & Ladouceur, 1996; Langlois, Freeston, & Ladouceur,
2000). More persuasively, based on experimental interventions designed to engage
different aspects of working memory, Rapee (1993) concluded that worry is basically
a verbal process. Worry was attenuated only on tasks that engaged the phonological or
articulatory loop (important in processing and storing verbal information), together
with the component of central executive control concerned with the phonological
loop8 (cf. Baddeley, 1990). Second, physiological findings suggest that verbal thought,
in turn, is associated with an attenuated cardiovascular fear response compared with
that evoked if individuals instead engage in imagery-related thinking involving the
same stimuli (Roemer & Borkovec, 1993; Vrana, Cuthbert, & Lang, 1986). Compared
with “ordinary” worriers, “excessive” worriers show both a greater predominance of
thoughts rather than images, and significantly attenuated autonomic hyperactivity
symptoms, including cardiovascular symptoms (Freeston et al., 1996). Third, there is
evidence that people may use verbalization as a way to functionally modulate and
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 69
reduce affect- or worry-related arousal (D. M. Tucker & Newman, 1981; see also
Mathews, 2004). That is, “people spontaneously use verbalization as a strategy for
abstraction, disengagement, and inhibition of emotional arousal associated with
arousing stimulus material” (Stöber & Borkovec, 2002, p. 89; see Holmes & Mathews,
2010, for review).
Consistent with this avoidance account of worry, in studies in which individuals
were instructed to either worry, or to relax, the instruction to worry was associated
with reduced mental imagery (e.g., Borkovec & Inz, 1990). In addition, individuals
with generalized anxiety disorder, who showed high levels of worry, also demonstrated
reduced levels of imagery overall (and also when instructed to relax), but this
difference was reduced following successful therapy.
One account of the mechanisms that lead to these reductions in mental imagery is
provided by the reduced concreteness theory of worry (Stöber, 1998). According to
this account, the verbal processing characteristic of worrying involves highly abstract
concerns, words and sentences, that act to prevent or minimize imagery, which is
much more readily, and more vividly elicited through concrete words and expressions
(e.g., Paivio, 1991; Rubin, 1995). Worry then leads to self-perpetuating, highly abstract
processing. Although processing of the relevant threat (both cognitively and emotion-
ally) is thereby minimized, like many avoidance responses, this offers little opportu-
nity for more focused problem solving. Continued avoidance also prevents the
individual from experiencing any corrective learning because he or she is unlikely to
encounter any counterevidence regarding the appropriateness of the worry.
Evidence in line with this reduced concreteness account is provided by qualitative
evaluations of the descriptions that people provide of their worries and the possible
origins and consequences of the problems about which they worry. Independent
raters were asked to evaluate the problem descriptions provided by participants for
how “concrete” they were, that is, “distinct, situationally specific, unequivocal, clear,
singular,” and how abstract, that is, “indistinct, cross-situational, equivocal, unclear,
aggregated.” There was an inverse relation between the degree to which healthy young
adults worried about a given topic and the concreteness of their problem elaborations:
The more they worried about something, the less concrete was the content of their
elaborations concerning it (Stöber, Tepperwien, & Staak, 2000). Individuals who
worried a lot about a given topic (e.g., running out of money; losing close friends)
provided possible antecedents and possible negative consequences of those problems
that were rated (by three raters, blind to condition) as less concrete and more abstract
than were the descriptions provided by individuals who did not often worry about the
topic. Similar outcomes were observed when individuals were asked to successively
state what it was that worried them the most about a given problem, in what is termed
a “catastrophizing interview” rather than providing problem elaborations.
The importance of reduced concreteness in the maintenance of worry and
rumination also was supported by a study that examined the nature and level of
specificity of individuals’ responses to a low-mood eliciting video (Cribb, Moulds, &
Carter, 2006). Participants first watched a brief sad film that depicted the release
of an elderly man from jail, followed by his failure to reintegrate with society and his
eventual suicide. They were then were asked to provide descriptions of the video. The
less concrete the participants’ description of the film, the greater was their tendency
70 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
toward ruminative thinking and toward what has been termed “experiential
avoidance”—involving a tendency to resist remaining in contact with particular
private experiences such as bodily sensations, emotions, thoughts, memories,
and images.9 In addition, there were significant correlations between rumination
and several forms of avoidance (cognitive, behavioral, and experiential).
More recently, C. Stokes and Hirsch (2010) adopted the novel intervention of first
training individuals who were high worriers to use detailed concrete sensory imagery
when thinking about neutral topics, and then asking them to worry about one of their
recurrent everyday worries using imagery (versus verbally). For participants in the
imagery condition, imagery was defined as “generating an image of the situation and
tuning in to what you can see, feel, smell, hear and taste in the image as though you
are actually there right now.” Participants were also helped through a particular exam-
ple in which they were asked to imagine that they were cutting a lemon (cf. Holmes &
Mathews, 2005). Compared with individuals who were first encouraged to think about
neutral topics and then one of their everyday worries in a highly verbal manner (i.e.,
“in words, sentences, and questions, as though you are talking to yourself”), those
who adopted an imagery-based approach to their worry showed significantly fewer
negative cognitive intrusions during a later baseline breathing focus task. (Notably,
consistent with the notion that engaging in imagery about a worry topic is a difficult
and unpracticed task for habitual worriers, several of the high worriers reported that
they were unable to follow the imagery instructions, whereas few reported that they
were unable to follow the instructions to worry verbally.)
The finding that worrying in images, rather than words, led to a decrease in nega-
tive cognitive intrusions is consistent with the notion that the verbal nature of worry
may, in part, be responsible for its maintenance and perhaps also its uncontrollability.
Considering the possible reasons why inducing worrying with imagery was associated
with a decrease in negative intrusions of the thoughts, the investigators point not
only to the highly abstract content of verbal worry but also to the frequently frag-
mented nature of worry, with the worry topics remaining largely unintegrated with
the individual’s broader knowledge and emotions:
Many worrisome thoughts are of the ‘‘what if…?’’ type, relating to uncertain
outcomes […] and thus it is plausible that they lack a specific context as
well as being rather fragmented. The abstract and fragmented nature of the
worrisome thoughts may allow the worrier to jump from one topic to another,
and reach catastrophic outcomes [that] exacerbate further worry intrusions.
In contrast, generating imagery may be a more helpful process. Imagery
appears to have strong links with memory; for example, Dewhurst and
Conway (1994) suggest that knowledge stored in long-term memory needs
to be accessed and searched in order to generate images. Thus generating
imagery may draw on autobiographical memories and the individual’s
knowledge of the world, facilitating a more specific and concrete mental
representation of the worry topic. (C. Stokes & Hirsch, 2010, p. 422)
The intervention may have been one of the first times that participants had
considered their worry topics using imagery, and the imagery that they evoked “may
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 71
have acted as an on-line test of their negative catastrophic ideas, leading to changes in
appraisals of the situation, either because the image did not correspond with their
previous catastrophic ideas, or because the catastrophic image generated seemed
unrealistic in light of their knowledge of the real world” (C. Stokes & Hirsch, 2010,
p. 422). Exposure to the feared topic in the presence of corrective information may
also have promoted the extinction of fear (Foa & Kozak, 1986).
Taken together, the evidence suggests that chronic worry or rumination, like
depression, may impede flexibly adaptive problem solving because it gives rise to an
excessive reliance on overly verbal and abstract thinking. Such thinking is too
extremely divorced from particular events and contexts, in all their sensory, motor,
cognitive, and emotional richness. Given that concrete problem elaborations are
important in enabling us to counteract or prevent perceived risks to our well-being,
then worry, like the overgenerality of memory in depression, may substantially impede
effective problem solving, and thereby perpetuate the worrisome problem focus
itself.10 From the point of view of the iCASA framework, both worry and depression
appear to limit an individual’s “oscillatory range” with respect to levels of representa-
tional specificity. Mental agility is impaired by being constrained to either end of the
levels of representational specificity continuum. Becoming caught up in abstract
and categorical thinking, as in chronic worry and depressive rumination, or, to the
contrary, being too closely wedded to concrete particulars, as we saw earlier in the case
of individuals with superior memory, are similarly detrimental to creatively adaptive
thought and problem solving.
again with no direct instructions to participants that the preinsight task might be
relevant to their problem-solving endeavors.
Thus, engagement in the Alternative Uses Task did not seem to fall prey to the
“inert knowledge” problem (e.g., Gentner et al., 2003; discussed later in this
chapter) that has often been reported in studies of transfer of problem solving, in
which individuals have knowledge but do not access or retrieve that information when
needed, and so fail to apply it to the problem at hand. Rather, training in the Alternative
Uses Task here facilitated later problem-solving performance even without the
provision of any overt guidance or hints that the cognitive processes used during the
initial task might be helpful in solving the new problems. In addition, the training
benefits were not confined to only those items that were used during training but
appeared to occur for objects that were not themselves directly involved in the train-
ing procedure.
Although the results of Chrysikou (2006) are consistent with an account according
to which the Alternative Uses Task intervention leads to greater adeptness at “goal-
derived categorization,” that then procedurally transfers to the subsequent ill-defined
insight problems, four other observations concerning the tasks and the comparison
groups, and also additional data from our own lab, point to plausible alternative,
although not necessarily mutually exclusive, interpretations. First, performance of
the Alternative Uses Task also involves training in variability of responding: Participants
were required to provide multiple, different, nonstandard uses for each object. This is
important in that the two comparison conditions (Simple Word Association and the
Embedded Figures Task) did not require such variability and, instead, participants
were asked only for a single response (the first word associate that came to mind, or
the one matching instance of an embedded figure). As argued in Chapter 5, there
is strong evidence that training in variability may itself be an important factor in
encouraging a more adaptively flexible problem-solving approach (e.g., Neuringer,
2002, 2004). Indeed, based on several early explorations of “training in originality,”
requiring participants to give new word associations to repeatedly presented items,
Maltzman (1960) concluded that there was a puzzling (but important) general
transfer of training effect from one task to another. That is, training in variability
generalized to different contexts.11
Second, the word association comparison task may have encouraged reliance on
readily available or highly accessible information, perhaps inducing a more automatic,
habit-based mode of processing or cognitive orientation. Continued adherence to this
“automatic” cognitive processing orientation would then be disadvantageous on
the insight problem-solving tasks, where the first or most readily accessible alterna-
tives are unlikely to be fruitful for reaching a solution to the problem. The initial
encouragement of reliance on readily accessible associations may have worked to
impede appropriate editing and persistent search in the insight problem-solving tasks,
where following such an automatic “path of least resistance” approach (T. B. Ward
et al., 2002) would preclude the discovery of precisely those solution alternatives
that do not readily come to mind. In contrast, the Alternative Uses Task may itself
have indirectly primed a broader “think different” mindset that might also “operate by
reducing the automatic activation of associations” (Sassenberg & Moskovitz, 2005,
p. 508). Indirect inducement of an increased (detrimental) reliance on automatic
74 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
Uses Task for a brief period of only 10 minutes not only lead to significantly enhanced
insight problem solving compared to that observed in control conditions but that this
intervention also significantly enhanced performance on a well-accepted measure of
fluid, visual-spatial analogical reasoning—the Cattell Culture Fair test (Cattell &
Cattell, 1960). In this test, for example, participants are shown incomplete progres-
sive series of abstract shapes and are asked to select the alternative, out of several
options, that best completes the series, or to select which, of several abstract figures,
does not belong with the others.
Whereas improved goal-derived categorization might be particularly important for
ill-defined problems, such as the insight problems, it is less clear that this process is
essential for approaching visual-spatial analogical problems in which the stated goals
and aims are clear. Thus, it appears that the Alternative Uses Task intervention may be
increasing cognitive flexibility more generally, and that an account strictly in terms of
facilitated “goal-derived categorization” may be too narrow. These findings are consis-
tent with the iCASA framework in that they suggest that interventions, such as the
Alternative Uses Task, that encourage movements between specific and abstract
processing, and/or between different levels of cognitive control, may enable more flex-
ibly adaptive problem solving, not only for insight problems that are often peculiarly
difficult and resistant to ready solution (e.g., Kershaw & Ohlsson, 2004; MacGregor,
Ormerod, & Chronicle, 2001) but also multicomponent tasks requiring novel, on-
the-spot relational reasoning.
1997a; Tun et al., 1998) and may “overweight” semantic information in making
memory decisions (e.g., K. J. Mitchell, Johnson, & Mather, 2003). Yet, notably, not all
older adults show this pattern. For instance, K. M. Butler and colleagues (2004) found
that it was particularly older adults who also showed comparatively lower scores across
several different measures of frontal lobe functioning and executive processes that
demonstrated higher rates of errors related to gist-based memory processing. In their
study, older individuals with higher frontal lobe function showed levels of false recall
that were very similar to those of younger adults.
In work in our lab, we attempted to evaluate the extent to which both older and
younger adults can intentionally alter the level of specificity with which they recog-
nize recently encountered objects and words (Koutstaal, 2006). To evaluate such
intentional control of retrieval specificity, we first presented older and younger adults
with a large number of pictures of common objects (e.g., an umbrella or a house key).
To help ensure attentive processing of the pictures, participants were asked to
perform a simple size judgment on each of the objects; participants were not told
that we would later probe their memory for the objects (that is, encoding was inciden-
tal). After this task, and a brief intervening task interposed as a short memory delay,
participants were given a test of their ability to recognize the objects that they had
been shown during the size judgment task.
Like many such recognition tests, the test consisted of three sorts of items: objects
that were exactly like those shown in the size judgment task (called “same” exem-
plars), objects that were not shown in the size judgment task but that were categori-
cally similar to one of those items (e.g., a different umbrella than the one shown in the
size judgment task, called “different exemplars”), and objects that were unrelated to
the objects shown in the size judgment task (e.g., a giraffe, called “novel” or unrelated
items; items in these three conditions were counterbalanced). However, rather than
asking participants to make simple yes/no decisions regarding whether the objects
were old (shown during the size judgment task) or new (not shown in the size
judgment task), we asked participants to make one of two different sorts of recognition
judgments for a given item. In one judgment, the “identical” or “item-specific”
judgment, participants were told to call an item old only if it was identical to one they
had seen during the size judgment task. In another judgment, the “conceptual” or
“category-based” judgment, participants were instructed to call an item old both if it
was identical to one that they had encountered earlier and if it was similar to, or
categorically related to, an item they had been shown. (See, for example, L. M. Reder,
Wible, & Martin, 1986, and Reyna & Kiernan, 1994, for other work using variants of
the identical vs. meaning-based recognition instructions.)
There were two further important aspects of the procedure. First, each participant
was asked to make some recognition judgments that were “identical” and some that
were “category based.” Second, and most important, we provided the instructions as
to which of the two types of memory judgments they were to make immediately before
each test item—and these instruction cues to participants to query their memory in
an item-specific manner or, instead, in a category-based manner themselves changed
in an unpredictable and intermixed way. Thus, for some objects participants needed to
query their memory for detailed item-specific knowledge to make the item-specific
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 77
recognition judgment, and for others they needed to make only a more general
category-based recognition decision.
We found that, overall, both younger and older adults were able—to some degree—
to flexibly and appropriately move between making the item-specific versus category-
based recognition judgments (Koutstaal, 2006; cf. Ecker & Zimmer, 2009). In addi-
tion, older adults showed no deficits in the ability to make the category-based
recognition judgments: They performed on this task as well as the younger adults (see
L. M. Reder et al., 1986, and Koutstaal, 2003, for similar evidence of age equivalence
on tests of category-based recognition). However, overall, older adults showed a sig-
nificantly reduced ability to rapidly and appropriately change the extent to which they
responded on the basis of category information versus item-specific information in
response to instructions that required them to make either category-based or
item-specific memory decisions. That is, compared with younger adults, older adults
were less able to appropriately modulate the extent to which they relied on category
information, more often continuing to rely on categorical information when the
judgment required retrieval of highly detailed item-specific memory. Nonetheless,
conceptually consistent with the outcomes of K. M. Butler and colleagues (2004) that
had shown that not all older adults were equally susceptible to false recall, some older
adults demonstrated levels of “specificity modulation” that were equivalent to those
shown by younger adults.
Equally important, in further analyses, we found that specificity modulation in
episodic recognition in older adults was significantly positively correlated with other
measures of the ability to access and use other types of knowledge in flexible ways. For
instance, one common but quite straightforward measure to evaluate the efficiency
and flexibility with which a person can retrieve well-known information is to give him
or her a verbal fluency task. In the letter fluency task, participants are asked to state
as many words as they can that begin within a given letter (e.g., the letter “F” or “S”)
within a specified period of time (e.g., 1 minute). Similarly, in the category fluency
task, participants are asked to name as many different objects or items of a given sort
(e.g., “fruits” or “animals”) as they can within the allotted time period. Often, partici-
pants also are asked to avoid giving words of a particular sort (e.g., words that have
fewer than three letters, and proper names). Performance on both the letter fluency
and category fluency tasks has been found to be impaired by damage to the frontal
lobes (e.g., Troyer et al., 1998), and it is believed to rely on executive function
processes such as strategic search, and flexible thinking or “set shifting.” For instance,
in order to continue to generate new examples of animals on the category fluency
task, one might switch from giving instances of domestic animals to thinking of dif-
ferent instances of wild animals, or of animals typically found in a different country.
We found that there was a significant positive correlation between older adults’
ability to appropriately and flexibly use, or to avoid using, gist information in response
to changing recognition instructions (“specificity modulation” of episodic memory)
and how many words that older adults were able to provide on the letter fluency task
(Koutstaal, 2006). There was also a significant positive correlation between specificity
modulation and the number of words that older adults provided during a semantic
category fluency task.
78 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
These findings show that the ability to alternate between item-specific detailed
memory and category-based abstract memory for recently experienced events
is significantly and positively related to the ability to adaptively and flexibly access
information from semantic memory—and potentially also with frontal or executive
function. This points to a possible connection between “flexible remembering” of
recent episodes and some forms of agile thinking.
A further recent study from our lab (Aizpurua & Koutstaal, 2010), likewise
using the flexible remembering task in older and younger adults but now also incorpo-
rating measures of novel, on-the-spot thinking, together with a more extensive set of
measures of frontal function and also a measure of semantic short-term memory,
provided additional support for such a connection. In this study, replicating the earlier
result, we again found that younger adults showed significantly greater appropriate
specificity modulation on the flexible remembering task than did older adults. In this
work, we used as our measure of specificity modulation, a measure based on fuzzy
trace theory known as “recollection rejection” (e.g., Brainerd & Reyna, 2002), which
provides an estimate of the likelihood that individuals will retrieve verbatim informa-
tion about the studied items (e.g., “sofa”) when presented categorically or semanti-
cally related lure items (e.g., “couch”). The mean recollection rejection score of
older adults (M = 0.38, SD = 0.18) was significantly lower than that of younger adults
(M = 0.58, SD = 0.16). This measure of specificity modulation was significantly
positively correlated (r(69) = .66) with a combined measure of fluid thinking, includ-
ing the Cattell Culture Fair test of fluid intelligence (Cattell & Cattell, 1960) and the
Block Design subtest of the Wechsler Adult Intelligence Scale–Revised (Wechsler,
1981), and also with a measure of semantic short-term memory or “conceptual span,”
r(69) = .47. Verbatim recollection was also modestly but significantly correlated with
a composite measure of frontal functioning, r(69) = .30. However, when we included
each of these factors (age, conceptual span, fluid intelligence, and frontal function) in
a simultaneous multiple regression, we found that the strongest and only significant
predictor of specificity modulation on the flexible remembering task was fluid
intelligence. After accounting for the effects of fluid intelligence on specificity modula-
tion, there was no longer a significant effect of age, suggesting that the age effect on
the ability to appropriately and adeptly move between different levels of grain (item
specific vs. categorical) in episodic memory retrieval was largely due to the strong
association of age with fluid intelligence, r(69) =–.40.
Based on these findings, two further questions naturally arise: First, is it possible
to somehow enable older adults to reduce their task-inappropriate reliance on cate-
gory-based memory through training in the more flexible use of memory, and particu-
larly in specific memory retrieval? Second, especially in view of the theoretical account
of overly categorical memory retrieval in depression, are there conditions under
which healthy young adults also may show similar overreliance on category-based
memory—especially through manipulations that (like aging or clinical depression)
might lead to sustained changes in their “default” level of retrieval specificity?
The answer to both of these questions is yes. However, because evidence relating to
each of these questions also is very closely related to the important issues of the
representational processes of automaticity versus control, discussion of these findings
is deferred until Chapter 3.
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 79
to the effective transfer of knowledge to new situations. These studies have used a
diverse array of stimulus materials, populations, and types of thinking ranging from
analogies (e.g., Gick & Holyoak, 1980; 1983) to simple and complex forms of arithme-
tic and algebra problems (e.g., Bassok, Ling-Ling, & Olseth, 1995), to statistics and
physics problems (e.g., Bassok & Holyoak, 1989; Chi, Feltovich, & Glaser, 1981; B. H.
Ross, 1987), to various more applied topics, such as learning computer programming
languages (e.g., Adelson, 1981). Such inappropriate sensitivity to the surface details of
information in learning situations is assumed to play a prominent role in generating
what has been called the “inert knowledge problem.” As the term suggests, this expres-
sion refers to situations in which a learner has acquired and retained relevant knowl-
edge, but nonetheless this knowledge remains “inert”—not activated or successfully
accessed—under conditions where it is needed or would enable the solution of a prob-
lem (see, e.g., S. M. Barnett & Ceci, 2002; Bransford & Schwartz, 1999; Reeves &
Weisberg, 1994; for reviews). Such inappropriate reliance on surface information also
is difficult to circumvent: It is often only modestly overcome even by very direct and
deliberate means, such as explicit instructions to the learner to compare across differ-
ent examples or cases that they encounter, or direct reminders to the learner, before
the presentation of a new problem, that thinking about an earlier related problem may
prove useful for solving the current one.
But—granted the pervasiveness of the apparently “misguided” sensitivity of non-
experts to surface information—might there not be something positive and beneficial
in this proclivity? Is the retention of such details perhaps sometimes adaptive? And is
the apparent constriction and inflexibility of retention of surface details really as
broadly encompassing as it appears?
Here we will consider four points that strongly argue against an overly simplistic
view of impediments to flexible problem solving as arising from an excessive reliance
on surface details in learning situations. As developed later, the divide between rela-
tively more surface aspects and more abstract, structural aspects is neither as clear,
nor as sharp, as it has sometimes been characterized to be. First, such a divide largely
ignores the key role of physical embodiment (e.g., in language and other symbols) in
enabling and supporting abstract thinking. Abstract thinking does not occur in an
ethereal immaterial realm that is divorced from our sensory-motor and perceptual
functions, but in conjunction with (and often based on) specific material objects and
contexts. Second, claims regarding learners’ excessive reliance on surface details them-
selves need to be appropriately contextualized. Stated too broadly they represent an
overgeneralization on the basis of experimental work with particular sorts of materi-
als, especially ones that are relatively unfamiliar to participants; for more complex and
familiar materials there are many cases where individuals do spontaneously draw upon
more abstract knowledge and inferences, and abstract relational reasoning. Third, a
simple dichotomy of “surface” versus “abstract” (structural) features does not fully
accommodate the observation that even experts sometimes appropriately rely on
surface details because surface details often correlate with deeper structural patterns.
Such a divide also does not allow for learning-related shifts in the relative degree of
emphasis on different forms of representations, the concurrent presence of multiple
levels of representations of a given problem or problem domain, and the “bootstrap-
ping” from more specific to more abstract representations. Fourth, any simple divide
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 81
does not readily account for findings showing that there are substantial individual
differences in the extent to which persons benefit from abstract (rule-based) versus
specific (example-based) approaches, and also differences in the optimal timing of
these approaches (e.g., earlier vs. later in learning).
I N D I V I D UA L S D O O F T E N S P O N TA N E O U S LY R E A S O N U S I N G
A B S T R A C T R E L AT I O N S A N D C O N C E P T S
A further objection to the suggestion that we have an inveterate proclivity to attend to
only “surface-based” or superficial information is that such a characterization appears
to be inconsistent with a broader view of how individuals generally and most often
seek to understand and interact with the world and others. Rather, the evidence for
such an orientation (which is not being questioned) is more likely to itself reflect a
form of contextually dependent behavior.
Focusing particularly on the example of problem solving in physics, J. P. Smith
and colleagues explicitly argue for such a contextually dependent interpretation. They
propose that, although not necessarily “abstract” in the same manner as construed by
experts, individuals with less experience in this domain nonetheless bring to bear
other sorts of more experientially based abstract representations:
This argument in some ways closely parallels that made more generally by
Nisbett and colleagues (1987) with regard to the feasibility of the very broad goal of
“teaching reasoning.” Countering a pessimistic view about the possibilities of teaching
reasoning in a way that can yield generalization from one domain to other domains,
these researchers provide evidence for generalized learning of inferential rules but
also demonstrate that both the extent and form of generalization depend on the
underlying abstraction that is required.
To consider one example, these researchers found that there was initially consi-
derable domain specificity (that is, limited generalization) in the extent to which
individuals applied the law of large numbers. Whereas individuals were very likely
to appropriately use the law of large numbers when reasoning about the behavior or
outcomes of various types of randomizing devices (e.g., slot machines), they were
much less likely to use it in other situations where it might also apply (e.g., when
considering a small sample of an athlete’s behavior, or a single instance of a person’s
social behavior, such as whether they acted in a friendly or unfriendly fashion on a
given occasion). Yet when the wording of the problems was altered to make it more
apparent that the problem might be construed as a sampling scenario to which the law
of large numbers was relevant, then more participants correctly used the law in their
reasoning. Furthermore, both the frequency and quality of individuals’ reasoning
involving the law of large numbers was enhanced if participants were explicitly
trained in applying the law through any one of three methods: rule training, involving
abstract instruction in concepts relating to the law (e.g., defining such notions as
sample, population, and parameter, and showing that as sample size increases, the
sample usually more closely resembles the population); examples training, involving
the provision of particular examples (e.g., ability testing in a ballet company via
auditions; assessing someone’s sense of humor based on a first impression); or both
rule and example training. Although abstract rule training improved performance
across all domains, training on examples also led to learning that readily generalized
to new domains. These outcomes argue that people do possess an abstract law of large
numbers—and that many failures to apply it may arise not from not knowing the rule,
but rather from not noticing that a given situation is one where it might apply.
There is also evidence that, at least under some conditions, individuals do show a
clear ability to access more remote abstract relations across different situations
(e.g., Bearman, Ball, & Ormerod, 2007). One investigation examined retrieval of social
and interpersonal analogies that shared similar abstract themes (e.g., taking appropri-
ate action too late; reconciliation and learning from experience) but none of which
shared any explicit surface overlap (that is, no similar objects, characters, or event
descriptions). Wharton and colleagues (1996) found that although participants were
considerably more likely to retrieve close analogs that were high in both situational
and thematic similarity than remote analogs that were low in situational similarity
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 83
but high in thematic similarity, nonetheless they were more likely to be reminded
of remote analogs that shared a theme than of remote “disanalogs” that involved
moderate situational similarity such as a failure by both characters to obtain a goal,
but that differed in their theme. This pattern was observed even under conditions
involving incidental encoding (imageability ratings) and even with as long as a 1-week
delay, at least for these sorts of materials that were highly familiar to the partici-
pants.14 These findings argue that individuals can be reminded of abstract relational
parallels between quite dissimilar situations, at least in domains for which they have
substantial background knowledge, and under conditions that directly encourage
them to notice such parallels (also see Blanchette & Dunbar, 2001; Dunbar, 1995).
In summary, then, despite the evidence for what Gentner et al. (1993) termed the
“primacy of the mundane”—that is, the observation that most retrievals are literally
similar to the probe, in that they share both surface and structural characteristics
(very often, retrieval of “chair-1” leads to retrieval of “chair-2” and “chair-3” rather
than anything more exotic or esoteric)—and also for the presence of a “surface supe-
riority effect” (the observation that many retrievals involve only surface similarity
without structural similarity), neither of these comprise the entire story of what
sorts of information we are likely to bring to mind during everyday or naturalistic
problem solving. Rather, more abstract instances of retrieval involving only structural
similarity can, and do, also occur, though relatively rarely.
S U R F A C E I N F O R M AT I O N I S O F T E N “ VA L I D LY I N F O R M AT I V E ”
A N D M AY H E L P TO “ B O OT S T R A P ” A B S T R A C T I O N ; E X P E R T S
A L S O M AY R E LY O N S U R F A C E I N F O R M AT I O N
A further reason to wonder if the retention of apparently “superficial” details might be
adaptive is that the divide between experts and novices in terms of their degree of
reliance on surface details is not entirely sharp and clear. For instance, Hinsley and
colleagues (1997) and Blessing and Ross (1996) provided evidence of sensitivity to
superficial features even in nonnovice problem solvers. More broadly, and also more
encouragingly, considerable evidence suggests that—if selectively used—surface details
may enhance problem-solving performance, even in individuals with high levels of
expertise. In part, this is because even if “remindings” (Ross, 1984, 1987) of earlier
similar problem instances are based on superficial similarities, such similarities in
many domains are themselves positively correlated with structural features (e.g.,
Bassok, Ling-Ling, & Olseth, 1995; M. W. Lewis & Anderson, 1985) and thus may
enable useful comparisons to be made. “People know that very often content and
structure are not merely correlated by chance and that such correlations might be well
justified” (Bassok et al., 1995, p. 365). As observed by Medin and Ortony (1989,
p. 182), this link “enables surface similarity to serve as a good heuristic for where to
look for deeper properties” and, may, indeed, function as a not-too-tight “constraint on
the predicates that compose our mental representations”—helping to support “a notion
of similarity that is flexible without being vacuous.” These researchers argue that:
… organisms have evolved in such a way that their perceptual (and concep-
tual) systems are sensitive to just those kinds of similarity that lead them
84 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
Simply stated: “Quick access on the basis of surface content, even if it is not
guaranteed to be correct, may be an attractive initial hypothesis given the longer time
required for determining the deep structure. [. . .] It would be a strange expert who
could not take advantage of the strong predictive relationship between content and
deep structure” (Blessing & Ross, 1996, p. 806).
Furthermore, as also observed by Medin and Ortony (1989, p. 182), “perceptual
similarity based on representations of what appear to be more accessible surface
properties provides an initial conceptual structure that will be integrated with and
differentiated into the deeper conceptual structure that is acquired later.” What
begins with surface similarity need not remain there.
Such superficial or surface-based remindings may lead to the abstraction of
problem-schemata in indirect ways. That is, repeatedly using earlier problems to solve
current problems may lead to incremental refinements in the earlier reminding-based
generalizations (Ross & Kennedy, 1990; Ross, Perkins, & Tenpenny, 1990), so that the
recognition of superficial similarities between two situations or instances helps to
“bootstrap the formation of more abstract similarities between them” (Goldstone &
Sakamoto, 2003, p. 455). For instance, 4-year-old children could more readily perceive
an abstract symmetry relation shared between two situations if they were first
given practice with literal similarity comparisons in which the situations shared both
superficial and abstract similarities (Kotovsky & Gentner, 1996). Even a concrete
comparison may promote the alignment of common relational structures; further-
more, this process of comparison may itself invite additional adjustments to promote
better alignments, making possible, in turn “even more abstract, or analogical, com-
parisons.” Thus, “this cycle can be seen as a kind of disembedding or decontextualizing
of relations from initially situated representations to representations that can be
matched across domains” (Kotovsky & Gentner, 1996, p. 2814).
More broadly, even if the ultimate objective is to convey abstract principles in a
given domain, it need not follow that the most effective means for conveying or for
instilling those abstract principles requires its presentation in a correspondingly
“abstract” form (e.g., via verbal propositions or mathematical statements). As will be
further developed in Chapter 4, there are many important advantages to presenting
information in a concrete, perceptually rich manner that enables sensory-perceptual
and perceptual-motor simulations (e.g., Barsalou, 2003) or that supports true infer-
ences from perceptual representations to abstract principles (e.g., Bassok, 1996).
Several important advantages of using relatively more concrete elements during learn-
ing are succinctly summarized in Table 2.1, reprinted from Goldstone and Son
(2005)—together with contrasting advantages that may result from the converse
approach, of using more idealized or abstract elements.
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 85
Although different in many ways, this approach is also reminiscent of what has
been termed a “recognition-primed” decision-making approach (briefly introduced
earlier in Chapter 1), which strongly emphasizes that expert decision makers in natu-
ral settings “use situated content-driven cognitive processes to solve domain-specific
problems by taking concrete actions” (Lipshitz, Klein, Orasanu, & Salas, 2001; Klein,
2008; see also Fadde, 2009, and Salas et al., 2010). Cognitive task analyses of the deci-
sions made by experts, such as firefighter commanders, under high time pressure and
in very challenging incidents, showed that the decision makers did very little compar-
ing of options, and often seemed to consider only one option. Most often, they carried
out the very first action that they had identified as possible. Several factors may con-
tribute to such “single-option” decision making. However, one central proposal is that,
based on their extensive experience with multiple incidents, these highly experienced
decision makers very rapidly categorize the new situation on the basis of prototypical
or functional categories, based on particular salient features of the situation, thereby
enabling them to determine which goals make sense, which cues are relevant, what to
expect, and which actions typically work. Although this categorization may involve
aspects of analogical reasoning, it is not, in essence, the same as retrieving an analog.
Across a wide range of naturalistic decision-making contexts, considering highly
experienced military commanders, design engineers, offshore oil installation manag-
ers, and commercial aviation pilots, the recognition primed decision-making strategy
has been found to be used in as many as 80% to 95% of instances, with reliance on the
strategy decreasing for much less experienced decision makers.15 For instance, in one
study, of how experienced naval officers made decisions in a complex, time-pressured
command and control setting, a recognition strategy was used to identify 95% of the
actions taken. The recognition strategies predominantly involved feature matching,
involving familiarity with a typical class of situation; for example, to judge the threat
potential of an unknown aircraft, decision makers relied on salient features such as
country of origin, type of aircraft, flight profile (altitude, speed, bearing) and so on
(Kaempf, Klein, Thordsen, & Wolf, 1996). More broadly, Rothrock and Kirlik (2006)
propose that such strategies can be described as relying on “a disjunctive collection of
conjunctive rules.” On the basis of their analyses, they propose that candidate rule
sets are evaluated on three dimensions, including completeness—“the inferred rule
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 87
base is consistent with all operator judgments,” specificity—“the rule base is maximally
concrete,” and parsimony—the rule base contains no unnecessary rules” (Rothrock &
Kirlik, 2006, p. 145). Such characterizations provide increasingly specific and princi-
pled guidance regarding the conditions under which reliance on concrete details is
likely to enhance problem-solving performance at varying levels of expertise.
I N D I V I D UA L D I F F E R E N C E S I N E M P H A S I S O N A B S T R A C T V E R S U S
S P E C I F I C I N F O R M AT I O N
Fourth, and finally, there may be substantial individual differences in the extent to
which persons benefit from abstract (rule-based) versus specific (example-based)
approaches, or differences in the optimal timing of these approaches (e.g., earlier vs.
later in learning). Although for some persons, at some times, superficial similarities
may help to emphasize abstract commonalities, for other persons, or at other times,
the superficial similarities may prove distracting, decreasing the salience of deeper
commonalities.
Two investigations by Goldstone and colleagues powerfully illustrate the impor-
tance of such individual differences. Using a complex dynamically adaptive computer
program, Goldstone and Sakamoto (2003) examined how perceptual similarities and
idealization influenced students’ transfer of an abstract scientific principle from one
domain to another. The students interacted with two computer simulations that were
governed by the same principle but that differed in the way in which the principle was
instantiated. For instance, students learned about an algorithm (simulated annealing)
for determining a good approximation to the global optimum for a given function in a
large search space, either in the context of balls falling on a hilly landscape or of finding
a route around several obstacles. Goldstone and Sakamoto (2003) found that students
who initially performed well on the computer simulation task (high-starters) were little
affected by the perceptual similarity of the analogous elements in the initial task versus
a transfer task using a similar principle: High-starters performed equally well under
the similar and dissimilar transfer conditions. In contrast, those who performed less
well initially (low-starters) showed far more accurate performance on a transfer quiz if
the analogous elements in the two simulations were dissimilar rather than similar.
This outcome was observed in three experiments, involving different measures and
manipulations of superficial similarity, and was further bolstered in a fourth experi-
ment, using a new task (competitive specialization), in which the initial simulation
contained either relatively concrete, or relatively idealized and abstract, elements.
Individuals who initially performed well on the simulation (high-starters) generally
showed a significant performance advantage with the concrete graphics during train-
ing, and they showed a higher percentage correct on a transfer quiz in the concrete
graphics condition than in the idealized condition. In contrast, persons who initially
performed less well were adversely affected by the additional detail; indeed, among
these students, only those in the idealized graphics condition showed significant
positive transfer.
In these experiments, participants themselves were often spontaneously
reminded of the relation between the earlier and the later simulations, so that super-
ficial-element “reminding” may not have been needed—and instead yielded costs,
88 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
particularly for those individuals for whom extracting the more abstract principles
was more difficult. This raises the possibility that, in some situations, concrete con-
struals may compete with abstract construals, and that individuals who are prone to
concrete construals may be particularly disadvantaged when concrete properties are
salient, or numerous, thereby “outweighing” abstract commonalities (Goldstone &
Sakamoto, 2003).
More recent work by Goldstone and Son (2005; see also Reisslein et al., 2010)
manipulated both the amount and the timing of the introduction of relatively more
abstract versus concrete elements as participants used computer simulations to learn
the algorithmic principle of “competitive specialization.” Notably, in this study the
researchers found clear learning benefits if the simulation was, at first, anchored in
concrete elements (e.g., the principle of competitive specialization was represented by
black ants competing for particular food sources such as an orange peach and red
apple) rather than more abstract idealized elements (e.g., less concrete depictions of
black dots and green patches that were, however, still explicitly described to the par-
ticipants as representing ants and food, respectively). Performance on a different
transfer task (involving pattern learning, but likewise using the competitive special-
ization algorithm) was greatest in what was termed a “concreteness fading” condition.
In this condition, participants were first introduced to the simulation with concrete
elements, but then these were replaced with more idealized elements halfway through
the first training phase. Transfer in this condition was higher than in any other condi-
tion, including conditions in which the elements were consistently concrete, consis-
tently idealized, or idealized and then concrete (termed the “concreteness introduction”
condition). Participants in the concreteness fading condition both made fewer errors
on a quiz querying their knowledge of the initial and transfer tasks (Experiment 1)
and showed faster solution times (Experiment 2) than in the other conditions. Also,
there was a significant interaction, such that although concrete elements in a simula-
tion produced better performance on the simulation itself compared to simulations
with idealized elements, the opposite occurred for the transfer simulation.
Concrete elements may be particularly useful early in learning because they reduce
the demands of mapping between different elements. Relatedly, as Schwartz and Black
have suggested (D. L. Schwartz, 1995; D. L. Schwartz & Black, 1996), concrete
elements may be beneficial because concreteness encourages people to reason about
the referent itself, and thus to use solution processes that have real-world analogs,
enabling what they term “strategic shuttling” between depictive models and abstract
rules. However, if only the concrete elements are used, then the individual’s construal
is likely to remain too contextually tied, with representations that cannot readily be
transferred from one situation (e.g., foraging ants competing for food sources) to a
superficially very different but abstractly analogous situation (e.g., pattern learning).
Other recent work, contrasting the use of more concrete (“grounded”) versus
abstract printed representations in the domain of early algebra in college students
showed that, for simple problems, there was a “verbal advantage.” However, for more
complex problems, a “symbolic advantage” emerged, such that for the complex
problems, the students performed better when solving equations than when given
the analogous problem in a story format (Koedinger, Alibali, & Nathan, 2008).
These researchers proposed that there are important tradeoffs in the computational
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 1 89
90
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 2 91
responding, and these studies have provided some initial intriguing outcomes
regarding whether certain aspects of our cognitive behavior are necessarily, or invari-
ably, automatic, or if they may, under the right conditions, be again brought under
intentional control. We then consider the effects of instructional sets that directly
encourage individuals to retrieve recently experienced events at a given level of
specificity on their ability to subsequently retrieve other events from the same time
and place, either at the same level of specificity or at a different (either more specific
or more abstract) level than they had initially adopted. Thereafter, we turn to several
further factors that may subtly alter, or shift, the level of representational specificity
that we use, potentially without our awareness of their doing so. Unconscious, unre-
flective, and automatic alterations in the ease with which objects and events are con-
strued at different levels of specificity are considered under three broad headings,
including environmental or contextual determinants of the level of specificity at which
we construe our own actions (“action identification”), psychological and temporal
distance effects on the “construal level” that we assume, and the effects of particularly
mild positive emotional or affective states on categorization and classification. Later
sections of the chapter consider, first, evidence that explicit instructions to use both
controlled analytical responding and also more automatic and familiarity-based
responding may improve performance on certain sorts of tasks, and then the possible
contributions of more automatic processes to adaptively creative analogical and
categorical problem solving. The penultimate section takes up the topic of the role of
unfocused attention and what has been termed “mind popping” in promoting agile
thinking. The chapter concludes with a broadly integrative overview of this and the
earlier companion chapter.
In conjunction, these findings suggest that this form of attentional and cognitive
training is particularly effective for individuals with a strongly reinforced (often
repeated) pattern of ruminative and depressogenic thought. Consistent with this
suggestion, other aspects of the clinical histories seemed to differentiate the groups
who had experienced three or more, versus two or fewer, previous episodes. The first
depressive incident in the “three-plus” group occurred significantly earlier in the
individual’s life, and these individuals reported greater childhood adversity than did
the two-or-fewer group, for whom the first depressive episode occurred later in life,
and who reported less childhood adversity. In addition, the therapy was most success-
ful in reducing the likelihood of relapse in individuals who had a clear history of recur-
rent depression, but who also had not experienced a significant adverse life event
immediately before the current episode. This suggests that the treatment was particu-
larly effective at intervening in overlearned cognitive patterns that were internally
generated, and that, once activated, might otherwise “recapture” the patient in
the rumination-avoidance-reduced executive processing cycle that was proposed by
J. M. G. Williams et al. (2007; see Fig. 2.3 in Chapter 2). In contrast, the intervention
was not necessarily effective in reducing the likelihood of depression in response
to painful significant life events that were of an external origin, rather than arising
predominantly from the individual’s internally generated maladaptive cognitive
responses to mildly stressful events.
Recent work also has examined mindfulness training in healthy individuals
(e.g., Chambers, Lo, & Allen, 2008; Zeidan et al., 2010) and has shown alterations in
attentional processes, particularly differential effects on what have been described as
“concentrative” versus “receptive” attention. In the characterization provided by
Jha and colleagues (2007), in the concentrative mode, “attention is restricted to a
specific focus”—such as one’s breathing. In contrast, receptive attention:
… is instead “objectless” and the goal is simply to keep attention fully “read-
ied” in the present moment of experience without orienting, directing, or
limiting it in any way. That is, attention is receptive to the whole field of
awareness and remains in an open state so that it can be directed to currently
experienced sensations, thoughts, emotions, and memories. Whereas extra-
neous stimuli are considered distractors in concentrative attention, in recep-
tive attention no stimuli are extraneous because attention is open to the
entire field of experience. (Jha, Krompinger, & Baime, 2007, p. 110)
These two forms of attention correspond to two commonly focused styles of medi-
tation, one of which, focused attention meditation, involves the voluntary focusing of
attention on a chosen object or thought, and the other, open monitoring meditation,
that involves “non-reactive monitoring of the content of experience from moment to
moment” (Lutz et al., 2008, p. 163). Nonetheless, some researchers suggest that, as
actually applied, most meditation techniques incorporate aspects of both types and
thus fall “somewhere along a continuum of mindfulness-concentration practice”
(Ivanovski & Malhi, 2007, p. 77).
In two experiments using a pretest/posttest design with undergraduates,
Wenk-Sormaz (2005) found that meditation participants showed significantly less
94 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
habitual responding than did the other groups. In one study, participants were
randomly assigned to one of three 20-minute conditions: a meditation condition, in
which participants followed audio-taped instructions for predominantly concentra-
tive meditation involving a breathing-focused stress-reduction technique, or to one of
two control conditions, including a rest condition, or a cognitive control condition.
On a color/word Stroop task, in which the names of colors or strings of Xs were
presented in different colors of ink, and participants were asked to name the ink
color, the meditation group showed significantly less interference from the conflicting
word (e.g., compared with the neutral X condition, meditation participants were
faster than were control participants to correctly say “red” in response to the word
“blue” printed in red ink). These outcomes suggest that there was a reduction in the
“automatic” reading of the conflicting words by the meditation participants compared
with the other groups. Stated differently, participants in the meditation condition
showed greater adaptive flexibility in how they processed the stimulus materials on
the Stroop task, in that they were more able to selectively focus on one particular
perceptual aspect of the stimuli as required by the task (the color of the ink), and less
likely to be “captured” by a currently irrelevant but highly practiced response to the
stimuli (reading the word).3 Although a psychophysiological measure of arousal (using
participants’ galvanic skin responses) further showed, consistent with other research,
that the participants in the meditation condition also had a significantly larger reduc-
tion in arousal from pre to post testing than did the resting and control conditions,
the beneficial effects of meditation in reducing interference on the Stroop task
remained even when including change in arousal (arousal percent difference) as a
covariate.
In a second study, meditation group participants also produced more atypical items
than did controls (Study 2) on a generation task that required them to attempt to
produce atypical exemplars within a given category (e.g., a sport, a kind of money, a
vehicle) but not when, instead, typical items were explicitly or implicitly requested.
Additional analyses showed that high scores on a questionnaire measure of absorp-
tion, assessed with the Tellegen Absorption Scale and reflecting a “disposition for
having episodes of ‘total’ attention that fully engage one’s representational (i.e., per-
ceptual, enactive, imaginative, and ideational) resources” (Tellegen & Atkinson, 1974,
p. 268), also were related to the generation of atypical exemplars; however, the effects
of meditation remained significant even after taking into account the individual’s
ability to become absorbed in tasks by including absorption scores as a covariate.
Wenk-Sormaz (2005) concluded that, “across cognitive tasks, when participants
understood that the goal was to respond non-habitually, meditation reduced habitual
responding,” and that “meditation may result in honing the general skill of refocusing
attention on actions and cognitions that were previously habitual”:
It is likely that when this skill is used, the alteration of attention leads to
more flexible use of information through the encoding or retrieval of
information not typically used in that situation. This renewed information
availability supports less habitual responding by increasing the number of
response alternatives, thereby reducing the prominence of a habitual
response. (Wenk-Sormaz, 2005, p. 53)
F lexi bl y U sing Memor y and Categ or ic al K n owl e dg e, Part 2 95
Broadly consistent with this approach, S. L. Shapiro and colleagues (2006, 2008;
S. R. Bishop et al., 2004) have proposed that mindfulness practice leads to what they
call a “meta-mechanism” of “reperceiving,” and also four additional mechanisms
involving self-regulation, values clarification, cognitive, emotional, and behavioral
96 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
By developing the capacity to stand back and witness emotional states such
as anxiety, we increase our “degrees of freedom” in response to such states,
effectively freeing ourselves from automatic behavioral patterns. Through
re-perceiving, we are no longer controlled by states such as anxiety or fear
but are instead able to use them as information. We are able to attend to the
emotion, and choose to self-regulate in ways that foster greater health and
well-being. Through consciously (intention) bringing awareness (attention)
and acceptance (attitude) to experience in the present moment, we will be
better able to use a wider, more adaptive range of coping skills. (S. L. Shapiro
et al., 2006, p. 380)
found that two of these variables (values and flexibility) were significant predictors of
a composite measure of mindfulness and reperceiving or “decentering.” Yet these
variables did not explain all of the relationship between mindfulness/reperceiving
and symptoms/stress, suggesting that there is also a direct relationship between these
factors that is not accounted for by values and flexibility.
Taken together, Carmody and colleagues (2009, p. 622) suggested that the most
plausible interpretation of these findings is that “mindfulness and reperceiving
(decentering) are highly overlapping constructs and that both of these variables
change” as a result of mindfulness-based stress reduction interventions. More pro-
grammatically, they suggested (Carmody et al., 2009, pp. 623–624) that, from
a clinical perspective, it is important to continue research efforts to delineate “the
qualities of attending to experience that lead to well-being,” as shown by individuals
who take part in mindfulness training procedures, and to find “the most accessible
ways of cultivating those qualities, while at the same time keeping in view the possibil-
ity of more penetrating investigation into the underlying processes in consciousness.”
Equally important, but from the point of view of basic research, there is a real need for
additional studies involving fully randomized assignment to the meditation or mindful-
ness intervention versus the comparison or control conditions, and also for the inclu-
sion of comparison conditions that take into account the effects of motivational and
individual difference factors that may otherwise also differentiate the groups.
Notably, the final brief intervention study that we will consider in this section used
both randomized assignment and a more active comparison condition. Tang et al.
(2007; see also Tang et al., 2009) contrasted an integrative body-mind training inter-
vention given to undergraduate students with a body relaxation training control
group. Each group received 20 minutes of training for 5 days. The integrative body-
mind training intervention was distinguished by the effort to diminish the require-
ment for individuals to directly control their thoughts, and it combined several aspects
of body and mind techniques with features of meditation and mindfulness traditions.
As described by Tang and colleagues, the approach:
Furthermore, in another experiment with younger adults, but using related word
pairs (synonyms or near-synonyms) rather than common objects, we found a signifi-
cant and task-inappropriate increase in sensitivity to gist information on the final
item-specific test in the CCI group relative to the III group. This suggests that initial
category-based retrieval elicited a cognitive set toward accessing gist-based informa-
tion that was difficult to reverse or “undo” when the task situation and task goals
changed, and retrieval of item-specific information was required instead. Notably,
these effects were all found on measures of sensitivity, rather than response bias; no
significant effects on response bias were observed.4
The conclusion to be drawn is simple, but it potentially has broad implications:
Once more abstract, categorical retrieval is initiated, it may be difficult to return to a
more specific, more perceptually grounded, or exemplar-based level of retrieval from
memory, at least for events encoded in a particular spatiotemporal context. This con-
clusion is particularly noteworthy in that several aspects of the recognition procedure
strongly reduce the likelihood of observing such effects, because they act to support
high levels of item-specific or verbatim memory (and the category-based retrieval cost
effect reflects an attenuation of item-specific memory). For instance: The tests involved
healthy young adults, a minimal retention interval between encoding and testing
(all phases occurred within a single experimental session of approximately 1 hour),
the stimuli were detailed color pictures (for which memory is typically very good), and
substantial cues to memory were provided during testing (that is, the tests involved
recognition rather than free or cued recall, and one-third of the items presented during
testing were exact re-presentations of items that were encountered at encoding). Thus,
the level of representational specificity intentionally adopted in an earlier cognitive
state may subtly shift the ease with which we can thereafter access even extremely
recent episodic memories.
The shifts in level of specificity in these experiments occurred as a consequence of
intentional episodic memory retrieval. Yet other evidence suggests both that engag-
ing in a different task before memory retrieval may help to offset the costs associated
with a category-based orientation (Shwer & Koutstaal, in preparation), and that
processing shifts in level of specificity may be induced in multiple ways that do not
necessarily call upon explicit memory retrieval. Processing shifts in level of specificity
have been observed after such diverse tasks as: describing photographs at a more
categorical versus detailed level (e.g., Rudoy, Weintraub, & Paller, 2009), placing items
into a few (broad) categories rather than many (differentiated) categories (Ülkümen,
Chakravarti, & Morwitz, 2010), focusing one’s attention on the global or overall shape
of stimuli rather than their individual features or parts (e.g., Macrae & Lewis, 2002),
engaging in a perceptual task (Finger, 2002), or even imagining oneself in the near
versus distant future (e.g., Hunt & Carroll, 2008). Collectively, these findings are con-
sistent with the proposal that tasks may induce either “transfer appropriate process-
ing” or “transfer inappropriate processing” (J. W. Schooler, 2002; Chin & Schooler,
2008) with regard to the predominant level of specificity they encourage. Such modes
of processing may then carry over to other stimuli and tasks that may be quite
unrelated to the initial impetus for such processing (e.g., C. Brown & Lloyd-Jones,
2003; Dodson, Johnson, & Schooler, 1997; Perfect, Dennis, & Snell, 2007; Westerman
& Larsen, 1997), facilitating—or impeding—performance on the subsequent tasks
F lexi b l y U sing Memor y and Categ or ica l K n owl e dg e, Part 2 101
depending on the “match” in the level of specificity of the processing demands for the
two tasks.
E N V I R O N M E N TA L A N D C O N T E X T UA L D E T E R M I N A N T S
O F A C T I O N I D E N T I F I C AT I O N
Any action can be identified in many different ways. Representations of actions range
from more low-level characterizations that concern how the action is performed (its
details or mechanics), to higher level construals that focus on the meaning or outcome
of the action, that is, why it is performed or with what effect (its consequences and
implications). Research suggests that individuals most often attempt to develop
higher level representations of their actions, but this propensity toward higher level
identification may prove problematic if the attempted actions cannot be enacted
automatically (Vallacher & Wegner, 1987, 1989).
In one study aimed to more systematically evaluate the simple but important
question, “What do people think they are doing?” Wegner and colleagues (1984,
Experiment 2) offered coffee drinkers coffee in one of two cups. One cup was a typical
cup; the other cup was unusually heavy and weighed approximately one and a half
102 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
pounds. Whereas those who drank coffee from a typical cup chose descriptions of
what they had done that were quite abstract, such as “promoting my caffeine habit” or
“getting energized,” this was not true for those who drank from the peculiarly heavy
cup. Participants who had attempted to drink from the heavy, unwieldy cup chose to
describe their activity in much lower level, less abstract, terms. They described what
they were doing as “drinking a liquid,” “lifting a cup to my lips,” and “swallowing.”
Note that all of these descriptions are accurate characterizations of the activity
that the participants had engaged in. Yet what might seem to be irrelevant or merely
contingent circumstances regarding that activity—arising from a simple difference in
the weight of the cup used—substantially and significantly altered the descriptive
terms that the participants used to characterize their behavior and actions.
How do individuals choose the level of representational specificity at which they
describe what they are doing? Vallacher and Wegner (1987) propose three principles
that guide such “action identification.” The principles are stated in terms of the pre-
dominant or default level at which an action is typically identified, termed its “prepo-
tent identity.” The first principle is that an action is “maintained with respect to its
prepotent identity”—such that this is the level of abstraction that is most readily and
most often adopted. Second, “when both a lower and higher level act identity are avail-
able, there is a tendency for the higher level identity to become prepotent.” Third, “when
an action cannot be maintained in terms of its prepotent identity, there is a tendency
for a lower level identity to become prepotent” (Vallacher & Wegner, 1987, pp. 4–5).
The tendency to identify actions at relatively high (abstract) levels of representa-
tional grain derives from an individual’s attempts to achieve comprehensive under-
standing—leading to an emphasis on the causal and other effects of his or her
activities, such as socially conveyed meanings and self-evaluative implications
(Vallacher & Wegner, 1989)5. However, such high-level identifications may be quite
remote from the mechanics of action, and so, under some circumstances, may prove
inadequate guides to action performance.
Research has shown that individuals are likely to move down from a higher to lower
level construal of an action under conditions in which the action is difficult, unfamil-
iar, or complex. Individuals also are likely to move down in their construals of an
action when their performance of the act is disrupted, or when they are given negative
feedback regarding their performance (see Vallacher & Wegner, 1989, for review).
Notably, each of these conditions—when performing an activity is difficult or unfa-
miliar, or when it is subjected to interruption or direct or indirect indications that an
error has occurred—also comprise conditions that tend to evoke more controlled forms
of processing (W. Schneider & Chein, 2003).
The interplay and operation of all three principles of action identification theory
might be illustrated by considering a simple activity such as returning home from
school or the office. Often, a fairly high-level representation of “what we are doing,”
such as “returning home,” is adequate and meets with no contrary resistance from the
world or our own actions in the world. Now, however, imagine that you are returning
home (perhaps driving) in the midst of a torrential downpour. Under these conditions,
one’s attention is likely to focus on smaller subcomponents of one’s behavior, such as
ensuring that one is staying in one’s own lane, allowing enough space between the car
ahead and one’s own to stop quickly, and so on. Yet, should the downpour suddenly
stop, we would tend to soon “move up again” in the hierarchy. Over time, we are
F lexi b l y U sing Memor y and Categ or ica l K n owl e dg e, Part 2 103
P S Y C H O L O G I C A L O R T E M P O R A L D I S TA N C E
E F F E C T S O N “ C O N S T R UA L L E V E L ”
Construal theory (Trope & Liberman, 2003, 2010), like action identification theory,
proposes that the same event or object can be represented (that is, construed and
interpreted) at multiple levels. According to this approach, high-level construal entails
the construction of abstract conceptualizations of information about objects and
events. High-level construals “apply to a broad array of examples and selectively
include relevant and exclude irrelevant features of those objects and events.” Thus,
high-level construals “capture the superordinate, central features of an object or
event,” and abstraction of these “high-level immutable features conveys the general
meaning of the event.” By contrast, low-level construals involve the opposites of
each of these: According to this account, low-level construals consist of “subordinate,
incidental features;” at this level, “events and objects are unique and specific” (Fujita,
Trope, Liberman, & Levin-Sagi, 2006, p. 352).6
There are multiple, and pervasive, effects of the activation of high-level, versus low-
level, construals on a wide range of cognitive and motivational behaviors. The key role
of level of construal in motivational regulation and self-regulation will be considered
in Chapter 5, which focuses on motivational contributors to flexible (and inflexible)
thinking. Here, however, it is important to note that alterations in an individual’s level
of construal—including alterations achieved quite indirectly, through a manipulation
of an individual’s believed psychological and/or temporal distance from a particular
event, or from directing an individual’s attention to the overarching goals of actions
(the “why” of an activity) rather than the methods used for implementing actions
(the “how” of an activity)—may have clear cognitive effects, influencing the breadth
of categories used in classification tasks.
For instance, whereas the activation of a high-level construal leads to categorization
in fewer, broader, and more abstract units, activation of a low-level construal has the
converse effect: Categorization in more numerous, narrower, and more concrete units.
Participants asked to imagine that they would engage in several activities in either the
near future or the more distant future (e.g., having a yard sale this upcoming weekend
vs. sometime next summer), categorized and grouped objects related to these potential
scenarios differently depending on the nearness of the event (Liberman, Sagristano, &
Trope, 2002, Study 1). When imagining temporally near events, individuals classified
objects (e.g., 38 items that might be included in a yard sale, such as chairs, sweaters, a
crib, a candy dish, a fish tank, board games, a blender, bikes, coats, etc.) into significantly
104 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
more categories (M = 7.06 across four different classification scenario tasks) than when
imaging temporally more distant events (M = 5.90 for the four scenarios).
At a motivational level, the activation of different levels of construal also may affect
the relative weightings that individuals place on more central, primary features of a
situation compared with relatively more peripheral, incidental, or secondary features.
More generally, aspects relating to the physical or psychological distance of an indi-
vidual from an event or object may affect level of construal: Events that are imagined
in the distant future are conceived in more abstract and generic terms than are events
that are imagined in the near future, and the level of construal induced through such
imagining of the future may itself influence current cognitive processing (Förster,
Friedman, & Liberman, 2004).
In a series of experiments, Förster and colleagues (2004) found that participants
who were asked to envision themselves engaging in a task 1 year later (distant future
perspective) subsequently showed more effective problem solving on certain types of
tasks than did participants who were asked to envision themselves engaging in the
task only 1 day later (near future perspective) or participants who were administered
no temporal perspective instructions. These researchers postulated that imagining
oneself 1 year later would induce a more abstract mental construal set than imagining
oneself only 1 day later, and that this more abstract construal should yield a “transfer
appropriate processing shift” that would facilitate problem solving on tasks that required
an ability to move beyond contextually salient interpretations or ideas to a more
abstract or noncontextually embedded perspective. In line with this prediction, com-
pared with individuals in the “1-day-later” condition, participants in the “1-year-later”
condition were found to more often correctly solve both classic verbal insight prob-
lems (e.g., the prisoner and rope problem, Experiment 1), and also two types of picto-
rial puzzles, including the snowy pictures task, requiring the identification of a
particular form from among a great deal of visual noise or “snow,” and the gestalt com-
pletion task, requiring the perceptual restructuring of a stimulus so as to identify
a given form from a highly fragmented depiction (Experiments 2 and 3, respectively).
In contrast, consistent with the notion that a higher level of abstraction is not
always beneficial for problem solving, but that the “best” level of specificity depends
on the task demands, the relatively distant future time perspective not only did not
help, but significantly impeded, performance on a task requiring analytical reasoning
(Förster et al., 2004, Experiment 6; see also the “missing element” picture completion
findings of Wakslak et al., 2006, for a similar outcome). Participants in the distant
future condition solved significantly fewer problems from the analytical reasoning
portion of the Graduate Record Examination than did individuals who adopted
a perspective focused on 1 day later, or a control condition given no temporal distance
manipulation. Analytical reasoning tasks may require comparatively greater emphasis
on feature-based, concrete, and systematic processing rather than more holistic or
integrative processing. Analyses of additional measures of the participants’ transient
mood, of how much they liked the tasks, and of their expectancies regarding their
performance suggested that these factors did not mediate the beneficial effects of the
distant temporal perspective on the nonanalytical problems. Rather, the results were
consistent with an interpretation in which “thinking about the distant future elicits a
processing shift [. . .] toward abstract mental representation that is transferred to
F lexi b l y U sing Memor y and Categ or ica l K n owl e dg e, Part 2 105
subsequent tasks, thereby facilitating performance on [at least some] creativity tasks,
which require abstract thought, and undermining performance on analytical tasks,
which require relatively concrete processing” (Förster et al., 2004, p. 185).
Notably, and in marked alignment with the arguments to be made in the next
chapter, regarding the degree to which we “think with our senses,” a growing body of
evidence suggests that the underlying bases for these associations of greater temporal
and psychological distance with relatively abstract thought and processing, and the
association of nearer temporal and psychological distance with relatively concrete and
analytic thought, may, in part, derive from our actual physical experiences with objects
and events that are near versus distant in space and time (e.g., what we can see of
objects from a distance versus when we are close-up to them). These implicitly and
unintentionally elicited effects of psychological distance on our cognitive and percep-
tual processing may involve an automatic “overextended” association of different
sorts of psychological distance with one another (see especially, Liberman & Förster,
2009, for findings and discussion; also cf. Förster, Liberman, & Shapira, 2009; Förster
& Dannenberg, 2010). Greater psychological distance, whether that distance relates
to time, space, social relations, or possibility, may induce more abstract construals of
objects and actions, whereas psychological closeness or nearness on each of these
dimensions may encourage more concrete or analytical construals, in part because of
how physical distance actually changes our perception. What we can “see” and “know”
when physically near to, versus far from, objects or events, differs, and this learned
experiential knowledge, based on our physical senses and ways of acting in the world,
may be “mirrored” or analogically extended into our mental and conceptual world.
As stated by Liberman and colleagues:
Without denying the uniqueness of each distinction, we propose that they all
constitute dimensions of psychological distance. Their point of origin is one’s
direct experience of the “here and now.” Transcending this point entails con-
structing mental models of what is not directly experienced, and the farther
removed an object is from direct experience, the higher (more abstract) the
level of construal of that object. Lower-level construals enable people to be
immersed in the rich details of the immediate situation, whereas higher-
level construals enable appraisal of the general meaning that might apply
across a wide range of alternatives. Consistent with this proposal, […
research] suggests that different distance dimensions are mentally associ-
ated, that distancing on any of these dimensions is associated with higher
levels of construal, and that they have similar effects on prediction, evalua-
tion, and behavior. (Liberman et al., 2008, p. 1205)
T H E E F F E C T S O F E M OT I O N , E S P E C I A L LY M I L D
P O S I T I V E A F F E C T, O N C AT E G O R I Z AT I O N
Experimental research has shown that mild positive emotions often produce patterns
of thought that are especially creative, flexible, unusual, integrative, open to informa-
tion, and efficient (e.g., Isen, 1987, 1999; for review of the possible importance of the
“approach intensity” of positive emotions, see P. Gable & Harmon-Jones, 2010).
106 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
In one early series of studies (Isen & Daubman, 1984) it was found that persons who
had been exposed to experimental conditions intended to induce mild positive affect
categorized stimuli differently than did persons in control conditions. Individuals
recently exposed to one of a number of different minor forms of positive affect
“boosters” (e.g., the provision of refreshments during the experimental session, being
given a small present, or watching a few minutes of a comedy film) categorized stimuli
(common objects, such as clothing) in a more inclusive manner than did control
participants. When asked to sort stimuli into categories, individuals in the positive
affect conditions placed more stimuli together in a category group than did the control
individuals—indicating that they perceived more of the items as related to one another
than did the control participants.
A similar pattern was found when, rather than sorting the stimuli into the catego-
ries, the participants were asked to provide ratings of how typical each stimulus was
of the category. On this task, participants in the positive affect condition tended to
rate stimuli that were nontypical instances of the category as clearer members of the
category than did control participants. Notably, this difference in ratings was obtained
for what are well-known and well-understood semantic categories. For instance,
individuals in the positive affect condition judged that such items as “camel,” “eleva-
tor,” and “feet” were more clearly members of the category “vehicle” than did the
control participants, and likewise were more willing than control participants to count
items such as a “purse” and “cane” as members of the category “clothing”—suggesting
that the increase in positive affect enabled participants to see aspects of the exemplars
and the category that the control participants found more difficult to discern or failed
to see. (For evidence that positive affect also increases the likelihood that participants
will spontaneously generate such atypical category members, see Hirt, Levine,
McDonald, & Melton, 1997.)
Similarly, Kahn and Isen (1993) found that the inducement of modest positive
affect led individuals to categorize nontypical food category items (crackers, soup, and
snack foods) as belonging to a predefined product category. A mildly positive affective
state also led to greater variety in choices among potentially pleasant items, perhaps
because the affective state gave rise to “a greater recognition of the differences among
brands in a set or the unique features various brands offer” (Kahn & Isen, 1993,
p. 258). N. Murray et al. (1990) also found that a positive affective state led individu-
als to show more flexible categorizations than did participants not in a positive affective
state. Induction of a positive affective state led participants to form broader and thus
fewer categories when asked to focus on the similarities among exemplars, and to
form narrower and thus a greater number of categories when instead asked to focus
on differences among exemplars. (The first section of Chapter 6 provides a more
general consideration of the effects of positive affect on thinking and reasoning, and
notes that effects of positive affect are not always beneficial, but depend on such
factors as the “fit” between the forms of cognitive processing that are facilitated
through positive affect and the particular contextual and task demands at hand.)
Each of the three conditions considered in this section—(1) environmental or
contextual determinants of action identification, (2) psychological or temporal
distance effects on construal level, and (3) the effects of emotional state, particularly
mild positive affect, on categorization and classification—can significantly alter the
F lexi b l y U sing Memor y and Categ or ica l K n owl e dg e, Part 2 107
level of representational specificity with which we engage with, and seek to under-
stand, the world and our situation within it. All three can exert largely automatic,
implicit effects on representational specificity, such that we have little or no awareness
that they have done so. However, and equally important, it is also possible to at least
sometimes make each of those conditions an explicit deliberate object of attention and
to use knowledge gained from that deliberate conscious review to enable more flexible,
contextually appropriate, thinking and categorization.7 In the next section, we take up
the question of how explicit instructions to deliberately adopt a particular level of
specificity and/or level of control may influence categorization and problem solving.
normal, and the likely sources of abnormal patterns. The participants were taught
each of 10 diagnostic categories using a list of key features for each diagnosis; partici-
pants then also identified key features in four example cases from each diagnostic
category. The critical manipulation concerned what happened thereafter: Participants
were assigned to one of four instructional conditions: (1) an explicit “feature first”
condition, in which they were instructed to carefully identify all features present
before assigning a diagnosis; (2) a condition similar to the explicit feature first condi-
tion, but with an additional indirect or implicit instruction suggesting that some of
the cases presented during the test phase would also have been presented during the
training phase. This condition was termed “implicit combined” because it indirectly
hinted that the use of a more automatic familiarity-based approach might also be
useful, for instance, in deciding the diagnosis of cases that seemed similar to previ-
ously encountered cases; (3) a “similarity-based” condition, in which participants were
instructed to trust familiarity and to diagnose based on their first impressions, and
(4) an “explicit combined” condition, in which participants were instructed to use both
a feature-based and similarity-based approach. Participants initially worked through
10 ECG cases using these instructions, with support and feedback provided as needed.
Finally, they were given a further 20 ECG cases to read, 10 of which were novel and
10 of which had been presented during the training phase; in this test phase no feed-
back or training was provided. The key outcomes were the levels of diagnostic
classification accuracy achieved in the four conditions on this final test. The results
showed that the diagnostic accuracy of the two groups given either the feature first
(42%) or first impression (41%) instructions did not differ from one another.
Importantly, the groups instructed to use both strategies, either directly (56%) or
indirectly (53%), significantly outperformed the single-strategy groups.
These results support an “additive model” of clinical reasoning, at least for
novices to a diagnosis task: Using both a feature-oriented and a similarity-based
approach yielded higher accuracy than did adopting either approach on its own.
Notably, the overall levels of diagnostic accuracy achieved in all of these initially naïve
groups with limited task experience were equivalent to those achieved by second-year
medical students, but those who received the combined instructions demonstrated
diagnostic accuracy equivalent to that shown by second-year residents. The equivalent
performance of participants in the two single strategy conditions, that is, those given
only feature-oriented or only similarity-based instructions, is also evidence that it “is
inappropriate and unnecessary to caution students to avoid using pattern recogni-
tion” (Ark et al., 2006, p. 408), because predominant reliance on pattern recognition
yielded accuracy levels equivalent to that achieved by mainly using an analytical
approach. Furthermore, analysis of the features that participants listed in support of
their diagnoses showed no differences in the likelihood with which participants in any
condition identified features that were consistent with the correct diagnosis, though
individuals in the feature-first condition identified more features that were indicative
of incorrect diagnoses, and they also made more false alarms than did any of the other
conditions. These outcomes argue that “various reasoning/teaching strategies need
not be mutually exclusive and, in contrast, can complement one another, leading
to greater diagnostic accuracy when used together than when either an analytic or
non-analytic strategy is used in isolation” (Ark et al., 2006, p. 409).
F lexi b l y U sing Memor y and Categ or ica l K n owl e dg e, Part 2 109
This important conclusion was both bolstered and extended in a follow-up study by
these investigators (Ark et al., 2007) that used largely similar materials. In this follow-
up study, the diagnostic accuracy achieved by four groups was compared, including
groups that (a) were either explicitly encouraged, or not encouraged, to use a contras-
tive learning strategy (further characterized later), and (b) were also either explicitly
instructed to trust any sense of familiarity they might have when diagnosing test
cases, while also closely considering relevant features—that is, directly encouraged to
use a combined reasoning approach—or were given no instructions as to whether or
how to rely on familiarity versus feature analysis. The latter group allowed examina-
tion of the performance of individuals using a “spontaneous” or self-guided approach
to reasoning. Participants in the contrastive learning strategy conditions were encour-
aged to deliberately search for similarities and differences between the cases they were
learning, comparing diagnostic categories that were similar on the basis of their
having features in common, and categories that were known to be easily confusable.
Importantly, the second variable (explicit instructions to use a combined reasoning
approach vs. the “spontaneous” or self-guided approach) allowed examination of
whether individuals spontaneously use both more generic (automatic) familiarity-
based processes and more analytic (controlled) feature-based processes.
In line with several previous studies that have demonstrated benefits from
a contrastive learning approach (e.g., Catrambone & Holyoak, 1989; Gentner,
Loewenstein, & Thompson, 2003), diagnostic accuracy was significantly higher for the
groups that used the contrastive strategy. Particularly noteworthy here, however, was
the further finding that diagnostic accuracy was also significantly higher for the groups
that were explicitly instructed to use the combined feature-based and familiarity-based
strategies, compared to those not given such instructions. There was no interaction of
these variables (contrastive vs. noncontrastive, and combined vs. spontaneous,
instructions). Furthermore, a delayed test showed that the benefits of contrastive
learning, and of the explicit instructions to use both feature- and familiarity-guided
approaches, were still present on a delayed test that was given 1 week later.
The inference to be drawn is simple, but theoretically and pragmatically important:
Although people might naturally or spontaneously use combined reasoning strategies
to some extent, explicit direct instructions to use both automatic similarity-based
processes and controlled feature-based search appear to lead them to use combined
strategies more consistently—and leads to significant gains in accuracy—at least on
some forms of perceptual classification tasks. A key question for future research is
whether instructional interventions to use combined processing modes may also
prove beneficial on other types of reasoning and problem-solving tasks. As further
developed in Chapter 12 on some of the implications and applications of the iCASA
framework, it is important to determine whether similar benefits arising from a “dual
dialogue” between relatively more automatic and relatively more controlled process-
ing are found in other applied domains, including domains involving stimuli that do
not require mainly perceptually based judgments.
Such findings may also cohere well with increasing evidence that a comprehensive
account of human categorization performance will need to accommodate both “rule
induction” and “exemplar encoding,” and mechanisms that enable shifts of attentional
focus in each of these. A prominent example of such a model is the ATRIUM model of
110 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
relations” (A. C. Olsson, Enkvist, & Juslin, 2006, p. 1371). Only when participants
were explicitly asked to learn by memorizing the instances did performance accuracy
improve (under these conditions, judgment accuracy was well modeled by an exemplar
model).
These outcomes suggest that, as noted by A. C. Olsson and colleagues (2006),
“there may be nontrivial constraints on people’s ability to shift to the process that is
appropriate to the task” (p. 1381). Although sometimes such shifts do occur sponta-
neously, at other times they do not. Research by Ashby and Crossley (2010) using a
classification task that required trial-by-trial switching between declarative/
rule-based and nondeclarative/procedural categorizations similarly led the authors to
conclude that, although “trial-by-trial switching between declarative and procedural
category-learning systems is possible if enough cues are provided to signal the par-
ticipant which system should be used on each trial”—as was the case in an earlier
study by M. A. Erickson (2008)—“in the absence of such unambiguous cues [. . .]
switching does not occur automatically. Instead, participants perseverate with one
system” (Ashby & Crossley, 2010, p. 9). These authors speculate that, in the absence of
salient cues regarding which learning system should be used, there may be changes in
the interactions between the frontal cortex and basal ganglia, such that, although
simultaneous striatal-mediated procedural learning is not prevented, such procedural
learning is denied access to cortical motor output systems. This suggestion would also
account for an asymmetry in the pattern of results that they observed, such that use
of an explicit strategy impeded access to procedural knowledge, but not the reverse.
Specifically, they found that whereas separate pretraining on the rule-based compo-
nent of the final task led to perseveration in 10 of the 15 participants, when pretrained
on the procedural information-integration component 10 out of 16 participants
switched to rules during the final task.
Another possible contributor to the ease and/or likelihood with which shifts might
occur, as suggested by A. C. Olsson and colleagues (2006), is the relative success rate of
an individual’s early attempts during a task at using rule or cue abstraction versus
inferences based on similarity. If, in nonlinear tasks, early attempts at similarity-based
responding are successful, then participants may shift to using exemplar memory. If,
however, “both cue abstraction and similarity to stored exemplars yield poor judgment
accuracy early in training, it is possible that the participants return to their initial
default mode of cue abstraction, investing their energy in continued, and in these
tasks futile, attempts at ‘cracking the code’” (A. C. Olsson et al., 2006, p. 1381).
Thus, both too rigidly exemplar-based, and too rigidly rule-abstraction-based,
approaches to problems are possible, with detrimental effects on flexible, adaptive
performance in each case. Furthermore, this raises the possibility of “a more strategic
use of exemplar memory than traditionally assumed, in these cases perhaps better
aligned with explicit semantic inference (Juslin & Persson, 2002) rather than percep-
tual categorization (Nosofsky, 1984)” (p. 1381):
One logical critique of this view is that an unsolved target problem must be
matched to a base analogue on the basis of structural features, which may
not be known in sufficient detail for the target problem (if the structural
details of the target were known, presumably it could be solved without
resort to the analogue) (Reeves & Weisberg, 1994, p. 385).
If base-target matches are to be made at a level of abstraction above that of
surface elements (i.e., either at the level of goals or deep structure), subjects
must induce the causal elements from a target analogue to accomplish a
match, thereby achieving at least a partial solution and rendering less need
for a base analogue (Reeves & Weisberg, 1994, p. 386).
GUN BOW
BULLET ARROW
In the semantic task, participants were instructed to judge whether the four-word
set contained two conventional semantic relations, that is, whether there is “a common
sense way in which two things often do, or easily could, have to do with each other”—
with one relation in the left pair and one in the right pair (e.g., gun-bullet, bow-arrow).
In the category task, participants were asked to decide if the top and bottom word
pairs were “both members of a common category”—for instance, both gun and bow
are weapons, and both bullet and arrow are projectiles. Last, in the analogy task, par-
ticipants were asked to determine whether the four words constituted a valid or mean-
ingful analogy, for instance, since a gun shoots a bullet and a bow shoots an arrow, the
two pairs represent the same abstract relation and so comprise a meaningful analogy.
Participants answered each four word pair as “true” or “false,” with true trials inter-
mixed with false trials (e.g., rose-thorn, beach-wafer). Immediately after the four-
word trial, a single target word appeared, and participants were asked to name this
word out loud, as quickly and accurately as possible. In some instances the target word
was related to the analogy and also to the conventional semantic relation (e.g., “shoot”
following gun-bullet, bow-arrow); in some instances the target word was related to the
category relation (e.g., “beverage” following can-soda; bottle-beer), and in others the
target was unrelated, with unrelated targets occurring for both true and false trials
114 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
On the one hand, this suggests important to-be-explored avenues for potentially
increasing the likelihood that individuals will notice and use analogical relations in
ongoing processing, through appropriate (other- or self-initiated) guidance to develop
and set up a facilitative general attentional strategy—including a focus on relational
processing. On the other hand, and particularly in combination with other findings
pointing to many impediments to more abstract relational analogical processing,
these findings prompt recognition of the considerable complexity of the cognitive pro-
cesses that support analogical reasoning. “Analogical priming involves not just using
the relations between pairs of objects, but also using a higher order relation (i.e.,
sameness of relation) that holds between the two similarly related pairs of objects”
(Spellman et al., 2001, p. 391).
Nonetheless, additional findings showing that similarity of internal relations
between one item, or situation, enhances retrieval of a second (similarly related) item
or situation (Estes & Jones, 2006) argue that the human ability to, in William James’s
phrase, quoted at the beginning of Chapter 2, “intend the Same” clearly extends to
relational properties—and, under some conditions, may be relatively automatic (see
also Estes & Jones, 2009). For instance, under certain conditions, reading a prime
phrase “glass eye” may facilitate comprehension of a subsequent target phrase, such as
“copper horse,” because both phrases involve the relation “composed of.” Such facilita-
tion has also been found between relationally similar primes (“steel scissors”) and
lexically dissimilar targets (“straw hat”), suggesting that it is the similarity of the rela-
tion between the targets that leads to the processing advantage, rather than lexical
priming; that is, it is not necessary that the initial terms (steel-straw) be similar to one
another (as perhaps might be argued for glass-copper).
Relational priming of this form has also been forwarded as a possible account for
the use of analogies even in quite young children. Based on a diverse set of observa-
tions from developmental psychology, such as evidence that young children may solve
some forms of analogies and may use analogies spontaneously (e.g., Singer-Freeman
& Bauer, 2008; Tunteler & Resing, 2002; cf. Goswami, 1991), relational priming has
been suggested as a “choice candidate mechanism for a developmental account of
analogy, emerging from simple memory processes” (Leech et al., 2008, p. 363). Leech
et al. (2008) present a computational account of analogy, in which initial exposure to
a situation is taken to prime a relation that can then be applied to a novel situation to
make an analogy, and where “relations” are represented as transformations between
states. These researchers (2008, p. 372) propose that “complex analogies involving
systems of relations and simple analogies involving relational priming may use similar
underlying memory processes (e.g., pattern completion and relational priming)”—but
“in considerably different ways.”
Such an account also may provide a potential way to begin to address the “access
paradox” insofar as, first, complex analogies are not assumed to emerge in a single
step and, second, explicit structure mapping is not viewed as (invariably) necessary
for analogy to occur. Instead, explicit structure mapping is thought to hold for only
one subset of analogies. According to this account, “explicit structure mapping is a
meta-cognitive skill: a relational priming mechanism reveals a relational similarity
between two domains, but the reasoner can iteratively unfold this by repeatedly
applying the simpler mechanism over and over again to components of a domain in
116 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
order to extend the analogy or to discover where the analogy breaks down”
(Leech et al., 2008, p. 377).
On the one hand, it is clear that analogy can take many different forms, and situa-
tions can be such as to either bring the necessary “relations” readily to mind, as in
some simple analogies, or may make identifying such relations particularly difficult—
thus likely drawing more extensively on meta-cognitive and deliberate control
processes. On the other hand, the possibility that relational priming may be one
elementary process in this form of reasoning equally clearly merits further exploration.
The evidence for relational priming raises the possibility that the relations involved in
analogies may (at least sometimes) not be explicitly accessed or known. This, in turn,
may contribute toward a better understanding of both the ability to use and to match
“relations between relations” across human development, and to the growing evidence
for some sorts of “analogical thought” in nonhuman primates (e.g., Fagot & Parron,
2010; Flemming et al., 2008; Haun & Call, 2009; Thompson & Oden, 2000; for discus-
sion, see Wasserman, 2008, Premack, 2010; see also Engle Richland et al., 2010 for
evidence that cultural differences in attending to, and using, relational information
may influence the analogical performance of young children).
If priming of relations occurs, this also raises the question of the specificity of rela-
tional priming, with such questions as: Is there is a “hierarchy” of relations—more
general to more specific—with priming occurring at some levels but not others? Are
particular instantiations of some relations more representative or prototypical of a
given relation than others? With regard to the second of these questions, at least in
the case of one form of relation (that of part-whole) it has been shown that more pro-
totypical instances of the relation are more readily judged to be instances than are less
prototypical cases (Chaffin & Herrmann, 1988). It also has been argued that priming
may not occur for some extremely abstract relations and that some relations may be
more “transparent” than others. To take a specific example, according to one posited
taxonomic classification of general relations (Levi, 1978, cited in Estes & Jones, 2006),
nut bread, vegetable soup, and fruit tree are all classed together as instantiating a gen-
eral “have” relation. However, it is possible that whereas nut bread and vegetable soup
both instantiate the same relation of something like “contain,” fruit tree might instead
be an instance of a relation such as “produce.” Similarly, although both tire rim and
family cow might be construed as instantiating the general “of” relation (rim of a tire,
cow of a family) they might instead differ in their relational instantiations with the
former involving a part-whole relation and the latter a relation of possession (Estes &
Jones, 2006). Empirical examination of the levels of abstraction at which relational
priming may most often occur, and of further questions such as the consistency and
contextual modulation of such priming, is needed and will help to constrain accounts
of the roles that relational priming may assume in both analogical thought and
problem solving.
Other memory mechanisms, such as the priming of individual concepts, also might
automatically or implicitly facilitate problem solving. For instance, Schunn and
Dunbar (1996) demonstrated that participants who performed two unrelated
problems on successive days (a virus problem and a genetics problem) in which the
solution to the first problem involved a particular concept (inhibition) that was also
involved in the second problem achieved higher solutions on the second problem than
F lexi b l y U sing Memor y and Categ or ica l K n owl e dg e, Part 2 117
did participants in either of two control conditions. This was so even though neither
the participants’ on-line verbal protocols collected during the problem-solving task
nor postexperimental questioning suggested that the participants had any conscious
awareness that their experience with the earlier problem had helped them to solve the
second problem. Notably, the problems involved were ones known to elicit a bias
toward hypotheses involving the concept of activation (rather than inhibition); thus,
these outcomes suggest that recently primed concepts may become sufficiently readily
available to overcome biases toward different hypotheses.
This meshes well with other evidence that sometimes participants’ performance is
affected by exposure to a source problem, yet participants remain unaware of the
source problem even while applying it to the new problem. Such unwitting use of pre-
viously presented information has been demonstrated both by retrospective reports
of reminding (J. M. Mandler & Orlich, 1993) and, more persuasively, by the verbal
“talk aloud” protocols of participants elicited during problem solving (Lovett &
Anderson, 1994). The important role of unconscious priming of concepts in facilitat-
ing complex and novel problem solving also coheres well with ecologically derived
evidence that experts, such as scientists, are often unaware of the origins of their
hypotheses (e.g., Dunbar & Baker, 1994).8
found that performance on the Alternative Uses Task (and also on measures of
story creativity and a composite creativity score) was significantly correlated with
measures of “primary process content” in participant’s generations of a story in
response to a simple story topic about a man and a woman. Primary process content
typically included concrete references to sensations and perceptual disinhibition
(e.g., references to disorder in the external world), whereas secondary process content
predominantly involved more abstract categories and words (e.g., temporal references,
moral imperatives, instrumental behavior, abstraction, and references to restraint and
order).
Movements—or oscillations—between phases of highly focused versus defocused
attention may allow wider and deeper access to associations that are only remotely
or weakly associated with the problem at hand or with what is at the forefront of
conscious awareness (e.g., Martindale & Dailey, 1996; see Zabelina & Robinson, 2010
for a recent defense of “creativity as flexible cognitive control”). As remarked by
Mendelsohn (1976, p. 366), “relationships between sequences of thought (or ideas
and images, etc.) can be better formulated or detected when they can be attended to
and manipulated simultaneously” and—consequently—“the greater the internal
attentional capacity, the more likely is the combinatorial leap which is generally
described as the hallmark of creativity.” If one has become mentally “stuck” on an
approach that will not work, defocusing attention (or shifting attention elsewhere)
also can facilitate a shift toward other ideas or avenues, including what S. M. Smith
(1995) has described as “dissipation of fixation.”
One broad type of fixation—deriving from an overly abstract approach to objects,
and particularly arising from an abstract conception of the purpose for which objects
are designed—is “functional fixedness.” Because it seems to involve a peculiar insensi-
tivity to perceptual features of objects that might “afford” desired actions (J. J. Gibson,
1979; Vaina, 1983) or enable sought-for ends, this form of fixation will be considered
in the next chapter on “thinking with our senses.” Other instances of fixation may,
however, involve excessive specificity. Prominent here are limitations on imaginative
thought arising from an unintended reliance on recently encountered examples, or
individual features of such examples (e.g., Jansson & Smith, 1991; Marsh, Landau, &
Hicks, 1996; Marsh, Ward, & Landau, 1999; Smith, Ward, & Schumacher, 1993; see
also Kalogerakis et al., 2010, for evidence that design and engineering consultants fre-
quently spontaneously use analogies but also that project teams tend to mainly draw
upon a limited set of familiar knowledge sources, particularly from other product cat-
egories, that may constrain the possibility for more highly creative recombination).
“Exemplar-based” fixation occurs both for experts and nonexperts. In the case of
experts, Jansson and Smith (1991) found that design engineers showed “design fixa-
tion,” defined as “a counterproductive effect of prior experience on the generation of
creative designs aimed at solving a realistic problem.” In their study, all of the
engineers were given the same problem to work on, with one key difference: half of
the engineers were given a sample design, whereas the remaining half were given no
illustration. The designs generated by the engineers who were shown a sample
design embodied many of the characteristics of the sample design, and many more
such characteristics than did the designs proposed by engineers who were not pro-
vided an example beforehand. On its own, this mimicking of example features is not
F lexi b l y U sing Memor y and Categ or ica l K n owl e dg e, Part 2 119
necessarily problematic: if, for example, the characteristics that were carried over
from the example were especially functional, or met some constraint in a particularly
elegant manner. However, it was further observed that even negative features of the
examples were carried over into the proposed designs. This then seems to be a clear
example of an automatic reliance on specific instances that was detrimental to
creatively adaptive problem solving. Nonetheless, this does not imply that examples
are necessarily detrimental: Rather, specific examples are, under some circumstances,
constraining on creative thought.
One reason that the effects of examples may be detrimental is that designers or
research participants often are not consciously aware that they are “fixated.” This is
shown, for instance, by little difference in the outputs of participants explicitly asked
to avoid the generation of solutions that are similar to the examples (e.g., Marsh et al.,
1999) and by the observation that designers—even those that study and teach design
on a regular basis—either do not appear to be aware of their “inadvertent” copying of
features of examples, or believe that the effect of the example solution on their
performance is positive, even though, in reality, they generate fewer ideas than con-
trols not exposed to examples, and also tend to reuse features from the example
(Linsey et al., 2010). Attempting to counteract the detrimental effects of examples
through providing designers with analogies and re-representations of the problem
through alternative categories was found to reduce fixation on some measures, but it
did not entirely eliminate it (Linsey et al., 2010). Presenting common examples rather
than unusual ones may lead to stronger links between the examples and generated
concepts, suggesting that common examples may lead to greater fixation than novel
ones (Perttula & Sipilä, 2007).
Notably, one’s own creative processes may also be the source of “examples,” and
thus it is important to evaluate if, and when, self-generated examples might help to
promote, or instead act to constrain, innovative thinking. Inspired by the creative
practices of many actual designers, recent work by Dow et al. (2010) demonstrated
that the serial (one-by-one) development of creative ideas, with feedback given after
the generation of each idea was linked with reduced creativity compared to a process
involving “parallel prototyping” (with several ideas considered concurrently). In the
parallel condition, novice designers developed three prototypes for a graphic Web
advertisement and then received feedback on all three prototypes; they then made
two more prototypes, received feedback on those two prototypes, and then made a
final version. In the serial condition, participants also created five prototypes and
then made a final version, but they received feedback after each prototype. Analyses of
the results showed that the advertisements generated by the parallel prototyping par-
ticipants obtained higher “click through” rates when posted on the web and experts
(editorial staff and ad professionals) rated the parallel ads to be of higher overall qual-
ity (across a set of five rating scales such as creativity/originality, tastefulness, and
adherence to graphic design principles). Independent raters also rated the parallel ads
as more diverse than the serial ads, and the parallel participants themselves reported
a larger increase in their level of self-efficacy related to their design abilities.
Several factors may have contributed to the higher innovativeness and diversity
in the parallel than the serial prototyping condition. Especially relevant here is
the way in which the critique of multiple ideas side-by-side may have both facilitated
120 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
comparison, and helped to prevent an excessive and too early or too exclusive focus on
refining a single idea:
directed thought were evaluated as, overall, more creative (though the pair-wise
difference between the groups was only marginally significant). The broader question
of when reliance on unconscious processes may, or may not, facilitate complex
decision making is taken up in greater depth in Chapter 7.
G. Mandler (1994; Kvavilashvili & Mandler, 2004) refers to ideas that may occur to
us in moments of nonfocused attention as “mind popping.” This phenomenon involves
the sudden emergence of ideas or semantic knowledge into awareness where the “idea”
was not intentionally sought. Often this occurs while individuals are engaged in rela-
tively automatic activities, with their attention in a diffuse (unfocused) rather than
concentrated mode (compare with the description of Jha and colleagues, 2007, given
in the first section of this chapter, of “receptive” versus “concentrative” attention):
In […] mind popping, a similar state of affairs occurs. The target is not
intentionally sought out; it is preconscious and thus has the characteristic of
fanning out, of engaging wider spreading of activation and more extensive
elaboration and activation. Thus, “thinking” about something else makes
it possible for the actual targets to become available for conscious construc-
tion. (G. Mandler, 1994, p. 24)
One should not dismiss the possibility that some states of passive thought
approach the sleeping state described by Hobson (1988), where quasi-ran-
dom neuronal activity significantly increases. If that can happen in some
awake states of passivity, then new elaborations (novel solutions) are more
likely to be generated. Such a state of affairs would be close to the ‘blind
variation and selective retention’ approach to problem solving advocated by
[D. T.] Campbell (1960). (G. Mandler, 1994, p. 25)
Possible trade-offs between more directed (focused) versus more open (broader)
receptivity to our own associative and other “thought connections” are further consid-
ered in Chapter 7. That chapter also considers the possible roles of both conscious and
unconscious thought during an intervening period of “incubation” in promoting new
approaches to a previously attempted but unsolved problem, and more controversial
claims that unconscious thought may increase “normatively correct” forms of complex
decision making above that found during deliberate thought. Trade-offs between
more focused versus broader receptivity to our own associative and other thought
connections are also addressed in the chapter that considers personality contributors
to flexible thinking (Chapter 6), including particularly the personality dimension of
openness to experience/intellect (Digman, 1990; L. R. Goldberg, 1993; R. R. McCrae,
1987, 1994), and the automatic attentional phenomenon of latent inhibition. The
phenomenon of latent inhibition, involving the ability to screen from conscious
awareness stimuli that have previously been found to be irrelevant, is itself a form of
cognitive control that may “cut both ways”—leading to more efficient processing if a
once irrelevant stimulus remains irrelevant, but impeding learning if contingencies
change such that what formerly was not relevant becomes predictive (e.g., Lubow &
Gewirtz, 1995; J. B. Peterson, Smith, & Carson, 2002). This possible trade-off—at
multiple levels—is also implicit in several of the “subcognitive” mechanisms of ana-
logical thought that Douglas Hofstadter (1995) has proposed and which may also sub-
stantially contribute to the astonishing “fluidity” of human concepts. Several of those
subcognitive mechanisms are explored in “Excursion 2” at the end of this chapter.
Looking Back
We began, at the outset of Chapter 2, and before embarking on these two companion
chapters, with William James’s affirmation, from his chapter on “Conception” in the
Principles of Psychology, that “The mind can always intend, and know when it intends,
to think of the Same.” The questions of how “sameness,” in the sense of categorical
knowledge of things, events, qualities, and relations might be represented and main-
tained in the mind and brain, are still centrally with us: They are an intensively active
focus of debate, analysis, and experimentation, and of healthy to and fro between
them. Yet we also have seen that individuals may find themselves in the tenacious grip
of a particular sort or “level” of sameness (either too specific or too abstract), as an
outcome of diverse cognitive-neuropsychological factors ranging from the automatic
recollection of highly detailed, vivid memories, involving an extraordinarily retentive
memory for particular sorts of events (instances of superior memory such as shown
by AJ), to prolonged and repetitive retrieval of experiences at an overly categorical
or general level, that too seldom reach into the richer, more specific recollection of
particular, singular events (clinical depression, healthy aging).
Although we can rely on both the retrieval of individual instances or exemplars, and
of abstracted rules or principles in ongoing thinking, classification, and decision
making—and both have advantages and disadvantages for the likely accuracy of our
performance—we do not always adroitly and aptly choose the best strategy for the
situation at hand. We sometimes rigidly persist in using a strategy that leads to
F lexi b l y U sing Memor y and Categ or ica l K n owl e dg e, Part 2 123
increased probability of error and slower or blocked learning and that may further
result in diminished creativity.
Collectively, the findings of Chapters 2 and 3 suggest that we also need to be
cognizant of a significant caveat to James’s claim: Our intentions to “think the same”
or “not to think the same” may not always yield the outcomes we hope for, and
sometimes the forms of “thinking the same” that we engage in are neither as fruitful,
nor as freely initiated (taken up) or forgone (stopped) as we might wish or intend.
Equally important, these and other findings on how we use memory and conceptual
knowledge have provided strong presumptive initial evidence for the claim that agile
thinking is optimally facilitated through dual dialogue between both levels of represen-
tational specificity (abstract-specific) and modes of control (controlled-spontaneous-
automatic), with no one place on these continua uniformly or always ideal. In the next
chapter, we further explore evidence for this claim. In Chapter 4 we turn to focus on
the many ways in which thinking, including highly abstract thought, is deeply and
pervasively interpenetrated and intermeshed with the concrete particulars of sensa-
tion, perception, and also action—bringing both the external world and our bodies in
relation to it, into mind.
mechanisms directly and explicitly refer to levels of specificity such as the “desire” to
build chunks based on samenesses or other types of connections perceived; the
relative levels of abstractness assigned to concepts; the degree of preference for
abstract descriptions over concrete ones; and differential rates of perceptual pro-
cesses—for example, spotting sameness versus relatedness. Other subcognitive
mechanisms proposed by Hofstadter less directly, but implicitly and partially concern
levels of specificity such as one’s willingness to adjust or destroy already-solidified
perceptual chunks; the degree to which activated concepts bias ongoing perceptual
search; the ease with which default perceptions can be overridden by a drive for
perceptual uniformity; and the degree of attraction to symmetry. Additional posited
subcognitive mechanisms concern potentially more enduring or transient characteris-
tics of an individual’s “semantic nets” or conceptual representations and their inter-
relations: the propensity for a dormant concept to “wake up” when lightly activated;
differential rates of spreading of activation from a concept to various semantic neigh-
bors; differential rates of decay of activation of various concepts; size of conceptual
halos of concepts; the manner in which perceptions affect interconcept distances; and
the probability of making a slippage between two concepts at a specific distance.
Finally, yet another cluster of proposed subcognitive mechanisms might contribute to
aspects of openness to experience and willingness to experience ambiguity or uncer-
tainty (to be developed in Chapter 5). Notable here are the following: a willingness to
let a “slippage” carry related “slippages” along on its coattails; willingness to accept
fragmentary mappings; willingness to consider alternatives even when there is no one
clear leading viewpoint; intensity of dislike of trivial or boring answers; and degree of
resistance to blending rival views, rival rules, rival answers, and so on—though this
last might, again, partially reflect the rigidity of one’s category boundaries or relative
category permeability.
Developing a detailed understanding of the nature of, and the contribution of, such
subcognitive mechanisms to the flexible use of categorical knowledge is essential.
Equally essential is the need to arrive at an integrated understanding of if, how, and
when subcognitive mechanisms are successfully and adaptively recruited during more
automatic versus more controlled modes of processing, and as we deliberately or
spontaneously move between different levels of representational specificity versus
abstraction at a more macro, overt, and conscious level.
4
Thinking with Our Senses
I am a noticer.
—Brenda Milner (in Csikszentmihalyi, 1996, p. 158)
Thinking seems to be a highly internal activity, a process that occurs inside our
mind, largely independent of the physical environment. Auguste Rodin’s famous
statue “The Thinker” conforms well to this view. The thinker leans over, resting his
chin on his hand, eyes staring unseeingly forward, all attention firmly focused inward.
But is this prototypical picture of the process of thinking accurate? Is this how “good
thinking”—and particularly flexibly adaptive thinking—most often or most
effectively occurs?
Insofar as our thoughts occur within minds that are not directly open to external
observation, the picture of thinking as an internal activity is, of course, correct. But
this is only a partial and limited construal of what is often a dynamic, deep, and
sometimes remarkably subtle interplay between internal “thoughts” and external
“nonthoughts” (processes, objects). Thoughts are also almost continuously guided and
shaped by external supports and influences.
Concretely embodied symbols, such as words and numbers are prominent
examples of such physical guides to thought. Although we often seem to simply “see
through” words to their meaning, words are also essentially physical: particular lines,
shapes, and forms on the page or computer screen in the case of visual text, sound
waves in the air for spoken speech, or particular patterns of movements in space and
time for sign language. These concrete physical aspects of written, spoken, or signed
language may subtly but significantly influence the directions of our thinking. Other
important and common physical guides to thinking and reasoning (sometimes termed
epistemic objects) include maps, graphs, diagrams, models, and so on.
Even thinking that appears to proceed without any overt reliance on such external
aids—such as thinking that is highly abstract—nonetheless builds on foundations of
mental concepts that are, at least in part, forged through an individual’s interactions
with the concrete world of sights and sounds, and embedded actions within it. Mental
representations are themselves grounded in perception, action, and feeling, and so,
too, therefore, is thinking—and creatively adaptive thinking.
125
126 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
The evidence in support of these broad claims, and for the critical role of “thinking
with our senses” in enabling adaptively flexible, creative thought, is vast and diverse.
It includes both a wide array of cognitive-behavioral findings and an equally wide and
growing number of observations from neuroimaging and neuropsychology, demon-
strating the essential role of brain regions that are involved in sensory and motor
processing in representing mental concepts. The latter encompasses not only direct
explorations of the role of sensory-motor cortices in the representation of concepts
(e.g., Chao, Haxby, & Martin, 1999; R. F. Goldberg, Perfetti, & Schneider, 2006; Kiefer
et al., 2008; Martin, 2007; Tranel et al., 2003) but also evidence for the recruitment of
sensory-perceptual processing regions during the recollection of earlier encountered
events (e.g., Polyn et al., 2005; M. E. Wheeler, Petersen, & Buckner, 2000), and
neuroimaging findings on the partial, but clear, overlap between brain regions that are
activated during mental imagery, when no external stimulus is present, and during
actual perception of a stimulus (e.g., Djordjevic et al., 2005; Grèzes & Decety, 2001;
Kosslyn et al., 1999; Kosslyn, Thompson, & Alpert, 1997; O’Craven & Kanwisher,
2000). The first section of Chapter 9 outlines several of these and further findings
that, together, demonstrate the concrete and multimodal—and abstract and
amodal—brain bases of conceptual representation.
In this chapter, the key role of “thinking with our senses” in enabling agile minds is
demonstrated through a consideration of four broad interrelated ways in which
thought and perception deeply and complexly intersect with, and influence, one
another. These include:
(a) Links between perception and conception within thinking, reflecting the
integral contribution of perceptual and action-related information to mental
concepts
(b) Demonstrations of how current perception (e.g., looking patterns) and
actions (e.g., gestures) may both guide, and sometimes precede, thought or
insight
(c) Contributions of perception and action to the flexible and generative use of
concepts or to innovatively “making new concepts”
(d) Links between perception and conception deriving from the embedding of
thinking in a particular concrete physical context, focusing on epistemic objects
and actions, and the role of the specific physical (sensory-perceptual) aspects of
language in shaping thought
The case to be made in this chapter is neither that we always think with our senses,
nor that we only think with them, but that we do so more often and in more ways than
we may realize.1 Furthermore, it will be argued that a failure to “think with our senses”
is at least sometimes the source of impediments to our thinking, and of the stultifying
and sorry character of some of our attempted forays into new avenues of thought and
action. The ways in which we do, and should, “think with our senses” are not limited
to simple or obvious physical actions or to our actual interactions with objects. They
are equally often important to complex modes of thought, such as hypothesis genera-
tion and testing, the formation and differentiation of complex abstract concepts, and
analogical problem solving.
Thinkin g wit h Ou r S e n s e s 127
Observation 1
Children aged 5, 6, and 7 years were presented with a task in which they were to help
“Bobo the Bear” reach a toy on a high shelf (German & Defeyter, 2000). The children
were presented a number of objects, including a box, several bricks, and various items
that were irrelevant to the problem solution (a coin, a pencil eraser, and a toy car). The
height of the shelf was such that a tower constructed from the bricks alone would not
allow Bobo to reach the shelf. To help Bobo achieve his lofty goal, it was necessary for
the tower of bricks to be mounted on top of the box.
If the box was presented separately from the bricks and the other items, with the
various items arrayed beside one another, then all children rapidly and easily solved
the problem. If, however, the bricks and other items were presented nestled inside the
box (emphasizing the function of the box as a “container”), then the older children—
very much like adults attempting to solve the analogous candle problem—were slower
in reaching the solution. That is, the older children showed clear functional fixedness.
This apparently slight rearrangement of the items made solving Bobo’s dilemma much
more difficult for the 6- and 7-year-olds. But this was not so for the 5-year-olds. The
youngest group of children showed no evidence of functional fixedness and solved the
problem equally quickly in the two conditions—and more than twice as quickly as did
the 6- and 7-year-olds when the containment function of the box was primed.
This age difference in performance, with the youngest children outperforming their
elder peers in the function-primed condition, did not reflect differences in knowledge
of the function of the box. The same outcome was obtained when all of the children
were first required to demonstrate the standard function of the box before being pre-
sented the problem (cf. Gauvain & Greene, 1994). For some reason, the youngest chil-
dren were immune to the harmful effects that the function-primed arrangement of
the objects produced for their older peers even though they, like the older children, did
know and understand the usual function of boxes.
Observation 2
Although younger children showed that they knew the usual function of a box, it
might be argued that, simply by virtue of their younger age, they had a reduced
knowledge store of specific experiences with boxes, and so might be less susceptible to
Thinkin g wit h Ou r S e n s e s 129
habit-based “blocking.” One way to test this account of the greater problem-solving
flexibility of the younger children would be to use objects that all of the children were
equally unfamiliar with before the experiment—that is, novel objects for which the
function was newly demonstrated for the first time in the experiment itself. If the
immunity to functional fixedness shown by the younger children results from fewer
encounters with the objects, then, once novel objects are used instead, this “naivety
advantage” for the youngest group should be eliminated, and all of the age groups
should show similar patterns of performance in the function-primed condition.
To test this account of the age differences, Defeyter and German (2003) developed
novel objects that none of the children would have previously experienced. One of the
novel objects was a “light stick,” used for causing red, yellow, and green light-emitting
diodes (LEDs) in a glass holder to light up. The other novel object was a “music stick,”
used to set off one of four buzzers in a gray plastic music box. The children first were
introduced to the novel objects and were shown their light-making and music-making
functions. They were then presented a problem in which the novel objects might be used
in a different way. They were told that a puppet named Zig was about to set out on a long
journey in a spaceship. However, Zig had encountered a difficulty: his pet dog, Tog, has
been naughty and has run away and become stuck in a long narrow tube. The children
were asked to show how Zig might help Tog out of the tube, using any of the objects.
As in other experiments exploring functional fixedness, the objects were presented
in one of two different configurations. In the baseline condition, all of the objects were
presented separately. In the function demonstration condition, the light stick and
LED glass holder were presented together as a functional unit (light stick + light
source), as were the music stick and music box (music stick + music source). One
further experimental manipulation concerned the shape of the light and music sticks.
Specifically, the length of the light and music sticks was varied, such that for one half
of the children the light stick was sufficiently long that it could be used to rescue Tog,
and for the other half it was the music stick that could be used to achieve this goal.
In the baseline condition, in which all of the objects were presented separately,
most of the children rapidly solved the problem. The solution rates were 75%, 95%,
and 80% for the 5-, 6-, and 7-year-olds, respectively. However, contrary to the “naivety
advantage” account, in the function demonstration condition, the solution rates of
the older children were again substantially lower, showing clear functional fixedness.
By contrast, the solution rate of the youngest group was entirely unaffected by the
function demonstration, again showing immunity to functional fixedness. In the
function demonstration condition the 5-year-olds achieved a solution rate of 75%,
clearly outperforming their older peers who had success rates of only 35% (the 6-year-
olds) and 40% (the 7-year-olds).
These outcomes demonstrate that functional fixedness cannot simply arise from
an accumulation of knowledge of the functions of real-world objects. Here, functional
fixedness was shown in the older children for novel objects that they had never previ-
ously encountered before the experiment itself. So what might lead to the older chil-
dren’s marked difficulties in the function-demonstration condition—making it so
difficult for them to see what the youngest children could see very rapidly, and what
other children in their own age group also could easily see under only a modestly
different perceptual arrangement of the objects? Why should older children perform
130 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
more poorly than did younger children specifically in the condition in which the novel
objects were grouped according to their (newly learned) functions?
Observation 3
Defeyter and German (2003) argue that the difference between the youngest and
oldest groups does not simply arise from differences in either the type or amount of
experience the different aged children have had with objects in the world, and the
findings with the novel objects support this proposal. The difference, instead, seems to
arise from a more fundamental and pervasive difference in how the older versus the
younger children think about human-made objects or artifacts.
Several lines of evidence suggest that, when adults reason about artifacts, they
take what the philosopher Daniel Dennett (1987) has called the “design stance.” The
design stance involves thinking about objects from the point of view of the creator,
maker, or designer of the object and the purpose for which the object was designed.
The design stance is an explanatory structure that explains why an artifact exists: its
function, its properties (e.g., its material, shape, and activities), and its kind (the type
of thing it is). Take the simple idea of a coffee mug. “A coffee mug is capable of contain-
ing liquids because that is what its designer intended. This intended function in turn
constrains its form (it must be closed at the bottom, open at the top, graspable when
filled with hot liquids, and so on) and also constrains the material from which it can be
made (e.g., not ice)” (Matan & Carey, 2001, p. 2). Although the properties that enable
a coffee mug to serve its intended function also, incidentally, enable it to perform
many other functions, such as holding pens or a houseplant, these are not the reason
the mug came into existence.
Adults often privilege the original intended function of objects in various tasks.
For example, if adults are asked to assign objects into different categories or classes,
they tend to categorize objects on the basis of their intended function rather than
either the object’s appearance or its current use. Similarly, they evaluate an object’s
function in relation to the original intentions of the designer rather than other
intentional or accidental uses to which the object might be put (e.g., H. C. Barrett,
Laurence, & Margolis, 2008; German & Johnson, 2002).
Evidence suggests that very young children do not necessarily adopt the design
stance. Rather, the predisposition to taking this viewpoint is something that develops
as children age, and it is consistently first shown by children sometime around 6 years
of age (though children do know the functions of objects much earlier, and sensitivity
to the intended function of objects can, under some circumstances, be shown as early
as 3 or 4 years of age; cf. Kelemen, 2004). For instance, 5-year-old children did not
prefer to classify a newly made object on the basis of what it was made for (e.g., catch-
ing rain water), over what it was currently being used for (e.g., trapping bugs), and did
not find the original function to be more important than the current one. Even if
4-year-old children themselves had made an object for a particular purpose (e.g., to
help pour lentils into a jar), and then later used it in a different incidental way (e.g., for
covering only the yellow parts of a yellow and blue picture), when asked what
they made the object for, these younger children found both the originally intended
function and the later serendipitous function equally good answers (Matan, cited in
Matan & Carey, 2001; see also German & Johnson, 2002).
Thinkin g wit h Ou r S e n s e s 131
It seems, then, that younger children have a less rigid or “more fluid” (German &
Defeyter, 2000, p. 708) idea of what can count as an object’s function than do older
children, or adults. Additional supporting evidence for this possibility has been
obtained by comparing the responses of children of different ages on a different type
of task. In the “Alternative Uses Task” (also previously considered in Chapters 2 and
3), the participant is given the name of a common object (e.g., a brick, a chair) and is
asked to suggest as many novel uses for the object as possible. The standard use of the
object is stated (e.g., a chair is usually used for sitting), and participants are asked to
give other possible uses (e.g., a chair might be used as a doorstop, as a hurdle, to break
a window in case of a fire, etc.). Although the Alternative Uses Task has often been
used to examine the ability of individuals to generate diverse or creative ideas, Defeyter
and German (2001; cited in Defeyter & German, 2003) were particularly interested
in contrasting the patterns of responses that were given by younger children, of about
5 years of age, compared to those given by slightly older children.
When 7-year-old children were given this task, the possible uses that they provided
tended to be minor variants on the standard function of the object (e.g., for brick,
“to build a house” might be followed by “build a wall, build a school, build a castle”).
But this pattern was much less noticeable in the uses suggested by 5-year-old children.
Responses of the younger children were likely to include other plausible uses of the
objects, beyond those congruent with the standard function (e.g., for a brick, “to stop
a door from blowing shut in the wind”).
Based on these and related findings, it seems that an important way in which the
younger children differ from the older children is that they place less emphasis on
what something is intentionally made for. For these children, other aspects of the
object, such as what it looks like, or what it is currently being used for, are just as
important as the object’s originally intended function. On these arguments, functional
fixedness does not arise from specific pairings of objects with their typical uses (a form
of experience-based habitual association), but rather from the way in which the
intended purpose for which objects are designed (in an abstract schematic sense) is
given priority over other possible considerations and features in our cognitive repre-
sentation—and our perception—of artifacts. That is, in many cases, functional fixed-
ness may arise from excessive abstraction and insufficient “thinking with our senses.”
S U P P L E M E N T I N G A N D C O M P L I C AT I N G T H E D E S I G N
S TA N C E A C C O U N T
There does, then, seem to be something special about original intentions—at least for
older children and adults. Nonetheless, an exclusive appeal to the “blinding force” of
the design stance is not fully satisfying. This account, too, is incomplete and raises
many questions. For instance: If objects are, by default, viewed from a design stance,
then why are the problems so straightforward to solve, by adults and older children
who have reached the “design stance” stage, in the baseline condition, in which the
object’s function is not specifically primed? Shouldn’t the object’s function also be
salient and prominent even in the baseline condition? Yet under the baseline condi-
tions, individuals do often flexibly see alternative functions of the objects, beyond
their most common, design-intended uses.
132 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
The design-stance account also does not seem to provide an entirely adequate
account of the findings from one of the earliest experiments on functional fixedness
(Birch & Rabinowitz, 1951), conducted with adults. This study showed a very strong
experience-linked disinclination to use one of two objects (an electrical switch or an
electrical relay) for a nonstandard function (as a pendulum weight so as to enable two
widely separated hanging ropes to be tied together) that depended on whether the
participant had earlier encountered the object while it served its designated function
(electrical switch vs. electrical relay). If participants were not given prior experience
with either the switch or the relay operating in its usual manner—but nonetheless
were highly familiar with such general sorts of objects through their electrical
training—then they were equally likely to use either the switch or the relay as a
pendulum weight to solve the two rope problem. This indicates that the physical
nature of these two objects was such that each could be adopted to serve this unusual
function. However, if participants had earlier used one of the objects in the standard
way, then they were significantly less likely to use that object for the pendulum. Both
those who had earlier been given experience with the electrical switch, and those
earlier given experience with the relay, gave plausible perceptually based reasons for
the superiority of the nonpreutilized object as a pendulum, relative to that of the
preutilized one (even though the control data argued that neither object was superior
to the other in this regard).
Birch and Rabinowitz (1951, pp. 124–125) suggested that these results pointed to
two different sorts of learning that may be important in problem solving, but that
differ in their degree of abstraction. The first sort involves the acquisition of “certain
broad, nonspecific, general notions about the properties of the object or method expe-
rienced.” They proposed that this type of learning might be typified by that shown by
chimpanzees in situations where, although they were initially unable to use a stick to
bring distant food within reach, they learned how to do so after a brief period of play
with sticks. “It is this general, broad, nonspecific experience which seems to provide
the repertoire of experience essential for productive thinking.” In contrast, the second
sort of learning acts to “convert the initial perception of broad general properties of an
object into perceptions of specific limited functional characteristics.” This narrow,
fixed learning “limits the range of perceptual organizations capable of being devel-
oped” by the individual, and thus interferes with problem solving.
These suggestions, and the earlier findings, prompt the question of whether there
are ways in which greater sensitivity or “attunement” to the sensory-perceptual prop-
erties of objects could be regularly achieved. One possible approach is that we might
physically or imaginatively rearrange the environment (physical or virtual) in which
we are attempting to move more flexibly. Arrangements of objects themselves “afford”
(E. J. Gibson, 2003; J. J. Gibson, 1979; Vaina, 1983) or offer to us certain uses. For
example, if we wish to reach a highly placed object, some elevated surfaces afford sup-
porting our weight (most chairs, step-ladders, rocks, tables) but others do not, per-
haps because they are insufficiently strong (a fragile child’s chair, perhaps) or
insufficiently stable (a rocking chair). The physical properties of objects constrain the
ways in which we can use them (e.g., whether we can grasp them) and how they can
interact with other objects (e.g., whether an object could bear the weight of a second
object). Altering the placement or relations between objects, either physically or
Thinkin g wit h Ou r S e n s e s 133
T H E S E N S O R Y - P E R C E P T UA L G R O U N D I N G O F C O N C E P T S :
C O G N I T I V E - B E H AV I O R A L E V I D E N C E
Imagine the following sequence of events (Case 1). You are sitting at a computer. First,
you are asked to read a sentence, shown on the monitor, such as “John hammered the
nail into the floor.” Immediately afterward, you are shown a line drawing of a nail.
Your task is to press the space bar on the computer keyboard as quickly and accurately
as possible if the object shown in the picture was mentioned in the sentence. In the
picture, the nail is shown as in Figure 4.1.
Now imagine the following sequence of events, with the same task requirements
(Case 2). First, you are asked to read a sentence such as “John hammered the nail into
the wall.” Immediately afterward, you are shown a line drawing of a nail. In the picture,
the nail is shown as in Figure 4.1.
In which of these two cases will you answer (press the space bar) most quickly?
Participants who were asked to do this task for a large number of different sentences
and objects were reliably faster in answering the questions when the orientation of
the picture matched the orientation that was implied by the sentence (here Case 2,
where the pictured nail is in a horizontal position congruent with that which would be
adopted when a nail is to be hammered into a wall) than when it was in a nonmatched
orientation (Stanfield & Zwaan, 2001). Across participants, this was true for both pos-
sible ways that the sentence could match the relevant object’s orientation, compared
to either of the nonmatching sentence-picture pairs.
Now imagine three other sequences of events:
(Case 3): First, you are asked to read a sentence such as “The ranger saw the
eagle in its nest.” Immediately afterward, you are shown a line drawing
If you now were asked simply to name the object shown in the line drawing, as quickly
and accurately as possible, would you be fastest in Case 3, Case 4, or Case 5? Or equally
fast in all instances?
Researchers (Zwaan, Stanfield, & Yaxley, 2002) found that participants were faster
to name the object in the picture if the shape matched that implied by the text (Case
4) than if it mismatched (Case 3). These outcomes are what would be expected if, when
they were reading the sentences, readers mentally generated or “simulated” the
implied shape of the object when reading and comprehending the sentence. Then,
when the shape that they had imagined matched the one shown in the picture they
could name the object more quickly than when the shape did not match the picture.
This result is remarkable given that naming and identifying common objects seems to
be such a simple, well-practiced, and largely “automatic” activity—but nonetheless
was influenced by the specific sensory-perceptual features that were recently mentally
activated, through visual imagery or something akin to a perceptual simulation, in
relation to the to-be-named object.3
Naming response times when the sentence was neutral, neither matching nor mis-
matching the picture (Case 5), fell in between the other two conditions. That is, the
naming response times were ordered as matching < neutral < mismatching. Although
it is not entirely certain why naming times in the neutral condition would fall in
between the response times for the matched and nonmatched conditions, one possi-
bility is that, when the sentences did not strongly bias any one shape of the object,
participants sometimes imagined a shape that matched the shape shown in the pic-
ture, and sometimes imagined a shape that did not match. If, by chance, they imag-
ined a matching shape for about one-half of the neutral sentences, but a nonmatching
shape for the other half, then the average of their naming response times would fall
about midway between the matched and mismatched conditions.
Additional evidence for the important role of something like perceptual simulation
in conceptual tasks derives from property generation tasks, in which participants are
asked to list the characteristics or properties of different nouns. If asked to provide
characteristics of “half a watermelon,” participants provided more features relating to
the interior of the object (e.g., black pips, white band of rind) than if they were just
given the word “watermelon.” It was as if participants had imagined the half melon in
the former case, and so observed more properties relevant to the interior of the
object that otherwise would have been occluded. Consistent with this suggestion, the
object properties that were generated when people were given specific instructions to
visually imagine the objects were very similar to the types of properties that were
generated by people who were given no specific instructions (neutral instructions) as
136 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
to how to perform the property generation task (Wu & Barsalou, 2004, cited in
Barsalou, 2003).
Based on these findings, it seems that, in order to think of the properties of an
object, individuals may spontaneously do something very much like imagining the
object. Features of objects may be brought to mind and identified using what Barsalou
(2003) calls a “perceptual simulation” of the relevant concept, as if, to use the concept,
we needed to imaginatively be there, perceptually or behaviorally, rather than remain-
ing an abstract, uninvolved, and disembodied (mental) user of a database. Concepts
thus are dynamic and active mental constructions rather than passive objects or data
points in our minds.
There were two important differences, however, between the properties given by
people with instructions to visually imagine the objects versus those given only the
neutral instructions. First, the participants who were specifically asked to imagine the
objects produced more properties than did those given the neutral instructions. This
observation suggests that the simulations performed by the participants in the neu-
tral condition were less detailed or less extensive than those who were given explicit
imagery instructions. Second, participants in the neutral condition did not always
respond in the same manner as those in the imagery condition. If the task conditions
were easy, such that participants did not need to rely on visual imagery to perform the
task, then there was less similarity between the responses of individuals given direct
instructions to use imagery and those who were given neutral instructions.
This last point is particularly important. For example, in one experiment (Solomon
& Barsalou, 2004), individuals were asked to indicate, as quickly as possible, whether
a given property (e.g., sleeve) was a “physical part” of the concept object (e.g., BLOUSE).
In the easy condition, the false property (e.g., chin) was unassociated with the concept
(e.g., BICYCLE). By contrast, in the difficult condition, the false property (e.g., tree)
was linguistically associated with the concept, but not actually a part of the concept
(e.g., OWL). The difficult condition discouraged people from simply relying on verbal
associations and, instead, required detailed perceptual “look-up” of the information.
In this condition, people who had been given neutral instructions performed very
similarly to people who had been given imagery instructions. Under these conditions,
perceptual qualities of the objects (e.g., the size of the to-be-determined property,
and the ease of finding the property in an image of the concept) predicted how quickly
and accurately the participants could perform the property verification task, both
for people given imagery instructions and for people given neutral instructions.
In contrast, under the easy conditions, the imagery and neutral conditions differed
from one another. Whereas perceptual qualities again predicted the property verifica-
tion performance of the imagery group, linguistic qualities, such as the associative
strength from the concept word to the property, best predicted the verification
performance of the neutral group.
Under easier conditions, participants appeared to rely on the verbal associations
of the properties with the objects, rather than perceptual simulation. Under these
conditions, they could just pay attention to whether the words seemed to be verbally
associated with one another (e.g., chin and BICYCLE are not associated) and base
their answer on this, saying yes if the things were associated and no otherwise.
But this strategy would not work when all of the word pairs were verbally associated
Thinkin g wit h Ou r S e n s e s 137
(e.g., tree-OWL; sleeve-BLOUSE), but only some were related in the required way, such
that the first concept was a part of the second concept. These outcomes suggest
that we often may fall back on using a simple word-association strategy in tasks
or problem-solving conditions where this is not explicitly discouraged or does not
interfere with successful performance of the task.
There is an expression used particularly in social psychology that characterizes
people as “cognitive misers” (Fiske & Taylor, 1984, p. 12). This expression is based on
the observation that people often tend to take shortcuts in thinking, using rules of
thumb (heuristics) and other strategies such as relying on general schemas or stereo-
types, so as to best use limited cognitive resources. Perhaps, though, we are sometimes
sensory-perceptual (and emotional) misers too. We may sometimes be overly ready to
respond entirely on the basis of comparatively abstract and sparse lexical or verbal
information, rather than on the basis of richer more fully embedded meanings that
also connect objects to the world of the senses—how something looks, sounds, feels,
tastes, and smells, and the ways in which we interact with it.
Our concept of a chair, for example, is not just an abstract list of features, but it
depends on a rich sensory-perceptual and sensory-motor understanding of chairs,
and particular chairs, including information from vision (what chairs look like),
from action (how hard or soft a given chair is or whether it is stationary or moving,
such as an office chair), touch (perhaps the coolness of leather or the grainy texture of
a fabric), and also emotion and motivation (e.g., a particular chair may be associated
with settling down to study intensively or with relaxation and listening to music).
Although we have such richly linked sensory-perceptual and sensory-motor networks of
meaning about simple objects such as chairs and watermelons, sometimes we bring to
mind only very small and restricted subsets of what is there. Sometimes we make little
connection to the sensory-perceptual features, traversing the deep world of meanings
largely through a suspended “surface net” of words and associations between words.
The perceptual simulation account thus suggests another way of conceiving
the processes that contribute to functional fixedness and other instances where we
simply fail to see what is there, getting stuck in one way of looking at a problem or
problematic situation. From the perceptual simulation perspective, functional
fixedness might be seen as the result of either a form of perceptual simulation that
fails or as the result of excessive reliance on verbal associative information rather than
perceptual information.
Would it help not to think about the objects as they are verbally labeled and
construed (“a candle, a box of tacks, a screen”) but more perceptually, and in relation
to motor imagery and sought-for goals: “what’s needed is a surface for mounting, and
a method of mounting”? Notice that, although such an attempted simulation is more
perceptual than is the verbally based labels description, it still is not extremely
specific, or object bound and context embedded (and so is more abstract, like the first
of the two types of learning described earlier by Birch and Rabinowitz, 1951). For
instance, consider a person who wishes to change the overhead light bulb in
Figure 4.2. The characterization, “what’s needed is a surface that will support one’s
weight and increase one’s reach” does not, in this case, call to mind only one specific
object, or set of objects, but instead allows for multiple instantiations. Simulations
may embrace the essential requirements to perform a given action, such as providing
138 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
a surface that will support one’s weight and increase one’s reach, without specifying
precisely the sort of object needed for that action.
In the illustration, the necessary surface might equally well be provided using
the chair, the stool, or the table. Any one of these meets the broad but perceptually
grounded characterization of “a surface for supporting one’s weight and increasing
one’s reach.” Thus, there are degrees of abstraction at the perceptual level as well—
and perceptual simulations need to be at the right level of abstraction to open up
Thinkin g wit h Ou r S e n s e s 139
the differing “instantiations” of the necessary parameters that are possible. At the
least, it appears likely that we might show greater flexibility in thinking if we
deliberately attempted to use alternative modes of conceiving a problem—relying
not just on the verbal construal or associations but also attempting to bring to mind
sensory-perceptual images, including a mental simulation of what’s needed for the
problem.
T H E S E N S O R Y - P E R C E P T UA L G R O U N D I N G O F C O N C E P T S :
FURTHER EVIDENCE AND THE ISSUE OF CONTROLLED
V E R S U S A U TO M AT I C A C C E S S
The findings from the easier property verification task used by Solomon and Barsalou
(2004), discussed earlier, suggest that, as also found in the case of functional fixed-
ness, sometimes we may excessively rely on verbal associative properties of objects.
However, whether we are likely to depend on predominantly perceptual versus more
abstract (e.g., functional) information concerning objects or concepts does not neces-
sarily involve a deliberate conscious choice, and there is evidence that sensory-percep-
tual contributors to concept “use” also may exert effects in more indirect, and largely
automatic ways.
One source of evidence for this derives from investigations of the ease with which
individuals can determine whether a given property is characteristic of an object—
and how the speed and accuracy of verification is affected by prior verification within
the same or a different perceptual modality, either across different but successively
presented concepts or for the same concept, presented at different times. In one study
(Pecher et al., 2003), participants were shown the names of different objects (e.g.,
LEAVES) and were then asked to indicate whether a given property applied to those
objects (e.g., rustling). The types of properties that were presented were drawn from
six different modalities, including vision, audition, taste, smell, touch, and action.
Sometimes the property that was given for one trial (e.g., LEAVES-rustling) was from
the same modality as that on the immediately previous trial (e.g., BLENDER-loud); at
other times the modality changed from one trial to the next (e.g., CRANBERRIES-
sour). The nouns that were used differed on every trial.
Participants were faster if the two successive trials involved properties in the same
modality than if they were from different modalities. This result would make sense if,
in order to verify whether, for example, a BLENDER is loud, we perceptually simulate
the sound of a BLENDER, but, in order to determine if, for instance, an APPLE is
shiny, we perceptually simulate the visual appearance of the APPLE—and these differ-
ent modality simulations take place using different brain regions or networks of brain
regions, rather than the same network for both. The brain might be more “efficient” in
using the same neural system and pathways that it had just used than if it had to
switch to a different (or mostly different) system.
These findings for the property verification task are also entirely congruent with
other results that have looked at the speed with which we can actually physically
perceive stimuli in the same perceptual modality or in different modalities. It has been
found that there is a “switch cost” associated with switching our attention between
different perceptual systems, that is, from vision to touch, or from vision to sound, and
140 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
so on, rather than attending to successively presented signals within the same modal-
ity. Participants were faster to discriminate whether a signal occurred on the left or the
right if the signal on one trial and the immediately following trial were both in the
same modality, allowing processing within the same sensory system (vision, signaled
by a light; touch, signaled by a touch on a finger; or audition, signaled by a tone) than
when the consecutive signals occurred in different modalities, requiring cognitive and
brain processing to switch between systems (Spence, Nicholls, & Driver, 2000).
More recently, it was shown that there is also a longer-lasting benefit linked to the
specific sensory modality in which we have recently considered a concept that can
remain even when we have been thinking about other concepts in between (Pecher,
Zeelenberg, & Barsalou, 2004). As in the earlier study, participants were presented the
names of objects, and then they were asked to decide whether a given property applied
to the object. However, now the name of each object was presented once, and then a
second time, sometime later in the experiment. The properties that were presented,
and that the participant was asked to evaluate, were either within the same sensory
modality (e.g., APPLE-green; APPLE-shiny; both visual) or in a different modality
(e.g., APPLE-green; APPLE-sour; involving a switch from vision to taste). There was a
significant response time advantage for the same-modality properties even when as
many as 12 or 18 different objects intervened between the two presentations of a
concept (mean median reaction time advantage of 34 ms and 41 ms for the 12 and 18
item lags, respectively). Participants also made fewer errors when the sensory modal-
ity for the first and second presentation was the same than when it changed. Only
when as many as 24 or 100 items were interposed between the first and the second
occurrence of a concept did the same-modality advantage disappear.
In the preceding investigations, changes in participants’ perceptual simulations
were instigated through changing versus holding constant the sensory modality that
was involved. Similarly strong evidence for the rapid and largely automatic effects of
perceptual simulation on individuals’ ability to access specific features of objects has
been provided by a rather different approach, involving manipulating the spatial per-
spective that participants adopt during sentence processing. In one study (Borghi,
Glenberg, & Kaschak, 2004), participants were given context sentences such as “You
are driving a car” versus “You are washing a car” and then were asked to answer verifi-
cation questions such as “Can you touch the headlights?” and “Can you touch the
wheels?” If the sentence context was such that it placed the individual on the inside of
the object (e.g., inside of the car) and the to-be-verified part also was located inside
(e.g., steering wheel, horn, fuel gauge, gas pedal), then these parts were verified more
quickly than if the parts (e.g., trunk, tires, antenna, door handle) were outside. The
reverse was true if the participant was imaginatively on the outside of the object; they
then verified outside parts more quickly than inside ones. In addition, for a given per-
spective, such as the inside perspective, objects that would, in actuality, be physically
nearer to the person from that same perspective were responded to more quickly than
were other objects that, although also potentially touched from that perspective,
would be farther away from the person. In contrast, objects external to the current
perspective were responded to more slowly, and similarly slowly regardless of their
distance. That is, if one could not touch the object from one’s current location, then
the magnitude of the part’s distance from one had no effect.
Thinkin g wit h Ou r S e n s e s 141
Additional analyses suggested that these perspective effects did not arise from dif-
ferences in semantic or associative relatedness; furthermore, the stimuli were designed
to make it very difficult for participants to rely on quick associative checks because the
nontarget probes were all associatively related to the target. For example, for the car
target, on the distracter trials participants were asked to indicate whether they could
touch the garage, road, taxi, and street—all requiring a “no” answer because none
are parts of a car, even though all are associatively related to the concept of car
(cf. the findings of Solomon and Barsalou, 2004, discussed earlier). These changes in
the accessibility of relevant (spatially proximate) information occurred largely auto-
matically or implicitly, as a consequence or by-product of mental simulation
(MacWhinney, 2005a, 2005b, Zwaan & Madden, 2005). These results seem to point to
what Borghi and colleagues called “an exquisite type of flexibility” (Borghi, Glenberg, &
Kaschak, 2004, p. 865), wherein alterations in perspective alter not only the readiness
with which individuals can gain access to information about particular object parts but
also to information about the spatial and functional relations among the parts.
Taken together, these and many related findings, clearly suggest that we do, indeed,
“think with our senses,” and that the effects of such thinking can be shown even on
simple tasks that appear to draw upon long-known simple facts about objects, such as
the color and taste of apples or the location of the horn or the steering wheel of an
automobile. Paying attention to perceptual details sometimes involves noticing fea-
tures and relations that are actually present “out there” in the world. But paying atten-
tion to perceptual details also sometimes involves noticing features and relations that
are only potentially available for us to retrieve from our “inside world” of stored knowl-
edge, memory, and experiences. It may also require abstention from a too ready reli-
ance on simple verbal-associative knowledge, and engagement in more imaginative
perceptual and sensory-motor simulations. Both forms of noticing are a key part of
what enables more flexible and more adept thinking. A further example of the central
role of such noticing in problem solving is taken up at the end of this chapter, in
Excursion 3, entitled, A Hypothetical Train of Thought: Perceptual Simulation in
Arthur Conan Doyle’s The Hound of the Baskervilles.
P E R C E P T I O N , P E R C E P T UA L S I M U L AT I O N ,
A N D H Y P OT H E S I S G E N E R AT I O N
If one has had a brief and introductory exposure to elementary distinctions in logic
and has discussed the differences between deduction and induction, one may well
have wondered: Is this really all there is? Are there not many situations where reason-
ing—and agile thinking—seem to depend on processes that are neither strictly deduc-
tive nor inductive? What about the processes involved when we are attempting to
solve a “mystery” or a puzzling set of circumstances, such as might confront a detec-
tive, or a scientist, with several disconnected pieces of evidence that appear to point in
quite different directions? Situations such as these, in which we are attempting to find
a promising direction of search—to decide which of many possible leads to follow and
which to reject as a probable dead end, so as to get closer to identifying the perpetrator
of the crime or the likely causes of an anomalous event or finding—certainly seem to
involve something like reasoning. But the form of reasoning involved is neither strictly
142 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
abductive inference shades into perceptual judgment without any sharp line
of demarcation between them […] the perceptive judgment is the result of a
process, although of a process not sufficiently conscious to be controlled, or
to state it more truly, not controllable and therefore not fully conscious. If
we were to subject this subconscious process to logical analysis, we should
find that it terminated in what that analysis would represent as an abductive
inference. (Peirce, 1901/1935, 5.181, p. 113)
should be looking may prove tremendously helpful. As Kaplan and Simon (1990,
p. 413) note: “The essence of discovery [. . .] is that you do not know beforehand where
the solution may lie. If noticing invariants, and in particular perceptual invariants,
provided even a little search constraint for the ill-defined task of discovery, then we
have a cause for celebration.” Perceptually grounded attentive thinking and “flexibility
in noticing” may allow us to bootstrap closer to an understanding of what really
happened or is happening in a mysterious series of events—whether those events
involve a dark and sordid crime, a deceptively simple brain teaser, or the real life but
often strange and unexpected mysteries that make a scientist’s world.4
In this connection, it is noteworthy that a recent attempt to develop a measure
of adult temperament, and to relate measures of temperament to well-established
personality dimensions, reported a very substantial correlation of r = .65 between the
Big Five personality dimension of “intellect/openness to experience”—related to
receptivity to new ideas and experiences and curiosity—and a measure of “orienting
sensitivity.” The latter measure might broadly be seen as an index of “noticing” and
included items assessing three forms of sensitivity: perceptual sensitivity, involving
awareness of slight, low-intensity stimulation arising from either the external or
internal environment; associative sensitivity, related to one’s noticing of automatic
cognitive activity, and affective perceptual sensitivity, concerned with one’s awareness
of affect associated with low intensity stimuli. The researchers comment that it was
surprising that, despite the large differences in the content of the items measuring
orienting sensitivity and openness to experience, these scales showed such a substan-
tial correlation. “It was surprising to note that orienting sensitivity, including
awareness of low-intensity stimuli, was related to much more complex personality
constructs like self-reported insight, reflection and imagination as measured in the
Big Five/[Five Factor Model]. In the past, the origins of openness have been much less
clear than for the other factors. Replication of this finding in the future and its
inclusion in developmental studies will be of great interest” (D. E. Evans & Rothbart,
2007, p. 882). The important contribution of openness to experience to agile thinking
is considered in Chapter 6.
problem was—as shown by the further finding that neither the number of features
recalled, nor the quality of recall, of the original General problem differed between the
three groups.
Rather, the physical enactment, particularly the process of showing, using the rect-
angular blocks, how the rebel’s forces might collide at the center (on the fortress),
seemed to increase the likelihood that the participants activated a “convergent force”
schema during the recall phase that could then be called upon again and successfully
accessed when confronting the radiation problem. Catrambone and colleagues argued
that, although a kinesthetic schema might encode structure, it is the fact that it was
possible to directly “read off ” the salient kinesthetic and spatial attributes (e.g., strong
at the center, weak at the periphery) that makes such a schema especially useful. More
broadly, they concluded that, “current models of analogical reasoning might be
improved by including perceptual information as part of their representational
schemes” (Catrambone et al., 2006, p. 1126).
These findings are congruent with two earlier demonstrations, by Beveridge and
Parkins (1987) and Pedone et al. (2001), showing the importance of animation and
perhaps implicit perceptual-spatial action in increasing the accessibility of the source
analog. Beveridge and Parkins (1987) found that the spontaneous generation of the
convergence solution among university students was increased to an astonishing 95%
when the “lines of force” in the source problem were first illustrated using six trans-
parent blue plastic strips that were hinged together at one end that was fastened to a
white sheet. The strips then were gradually “fanned out”—simultaneously showing
both a dispersion in intensity of the many “rays” as the color of the strips changed
from a darker to lighter blue and the summation of intensities at the center, where the
strips all overlapped and met one another, and so remained a darker blue. This highly
visual method of depicting both the summation and dispersion components of the
problem also yielded successful transfer in nearly a third of children, aged 10 to 11
years, who were tested.
Similarly, Pedone et al. (2001) showed that presenting participants with a diagram
of the source problem, particularly an animated (rather than static) converging arrow
diagram indicating motion toward the central point, markedly increased participants’
success on the subsequently presented target problem. Although these researchers
suggested that the representations underlying analogical inference might still be
largely amodal abstract schemas for convergence, they also considered that, either
instead, or in addition, the dynamic displays yield a “representation of moving forces
that is more purely perceptual than the kind of representation generated by reading
text” (p. 220). They argued that the solution to these problems depends “in a deep
sense, on understanding the perceptual and physical reality of how converging forces
interact with each other and with other objects that they contact along their
paths” and, further, that “this type of understanding may be best conveyed by
animated displays that generate rich perceptual representations” (p. 220).5
In conjunction, these outcomes strongly argue that the importance of “thinking
with our senses” extends also to the often creatively central process of analogical
reasoning, including beneficial effects of convergent support from visual, motor, and
kinesthetic representational processes. Yet neither the story, nor the case for “think-
ing with our senses,” ends here. The case is further bolstered by direct measurements
Thinkin g wit h Ou r S e n s e s 147
of individuals’ perceptual and motor activity itself during thought, for example, their
eye movements and gestures. Movements of our eyes or hands may not only support
analogical and other forms of problem solving but may in some instances reliably pre-
cede and perhaps provoke insight. It is to these ways in which our current perception
and physical actions can both support and advance agile thinking that we now turn.
on the tumor. The rays then will meet with sufficient combined intensity to
destroy the tumor but, because they pass through the healthy tissue in distributed low
intensities, they leave the healthy tissue unharmed.
What would happen if the perceptual attention of participants who were trying to
solve the problem were indirectly and surreptitiously drawn to the skin area? To test
this, Grant and Spivey (2003) performed another experiment, in which they again
presented participants with a verbal statement of the problem, together with a dia-
gram of the problem. However, in the experimental condition the circle that repre-
sented the skin area pulsed at a slow rate, thereby subtly “animating” the relevant
information. In the control condition, the diagram was either presented in a static
form, or a noncritical aspect of the diagram (the tumor itself) was subtly animated.
When the skin area was animated, twice as many participants reached the solution
than in either of the control conditions. Increasing the perceptual salience of the crit-
ical feature through the subtle animation effect in the skin region helped participants
to solve the problem.
These results suggest an interesting possibility. Although we generally assume that
where we look and attend is, if not irrelevant to how we think, then at least guided by
it, it may sometimes be the reverse—how we think may be informed by where it is we
look and attend. This possibility would cohere with the perceptual simulation account
that, in thinking about events or situations, we engage in “perceptual simulations” in
which we imaginatively act out interactions with objects and problem situations (see
Barsalou, 2003). From this viewpoint it is possible that participants’ “in-and-out eye
movements” themselves acted to initiate, or to “jump-start,”6 a perceptual simulation
of the multiple converging rays that, together, would allow destruction of the tumor.
How participants looked may have helped them to think more flexibly, so as to reach
this solution, or their looking may have been “ahead of” their conscious, explicitly
articulated problem solving.
Eye movements may also presage, or anticipate, explicit conscious steps in think-
ing in a quite different sort of task (Knoblich et al., 1999). “Matchstick arithmetic
problems” are arithmetic problems expressed in Roman numerals that are constructed
out of simple “matchsticks” (i.e., elongated narrow rectangles or matchstick shapes).
When first presented to the participant, each problem is incorrect. For example, the
expression
IV = III + III
is incorrect. The aim of the task is to change the problem so as to make the arithmetic
correct, producing a true arithmetic statement. However, according to the rules, you
must do this by moving a single matchstick from one position in the statement to
another. Furthermore, matchsticks may not be discarded, but can only be moved
within the problem. How can you solve this problem, moving just one matchstick?
The problem can be solved by moving the very first matchstick from in front of the
V and placing it after it instead, yielding VI = III + III. This is now a valid statement,
and it was achieved by changing the location of only one “matchstick.”
Participants who are shown problems of this general sort (Problem Type A) tend to
solve these problems quite quickly. However, they take much longer to solve another
Thinkin g wit h Ou r S e n s e s 149
sort of problem (Problem Type B), and sometimes simply cannot solve them, even
after a prolonged time period of attempting to do so:
When participants did solve problems of this sort, they often changed where they
tended to look when scanning the problems. The places they looked for relatively
longer durations, particularly during long visual fixations, were especially likely
to change from their earlier patterns of looking. Participants who were successful
at solving Problem B began to spend longer periods looking at the “plus sign” or the
operator in the problem. This change in where they looked both preceded and accom-
panied their insight into the problem. They thus were looking precisely where the
solution was, even before they had consciously become aware of how to solve the prob-
lem: Problem B is solved by changing the plus sign into an equal sign (III = III = III),
producing a true statement by, again, moving only one matchstick.
Successful resolution of Problem B, or other problems like it, requires that we
overcome an initial assumption about the nature of arithmetic problems. We assume
that the values in the equations are the variable elements, and so might be changed
to make the equation valid, but that the operators are constants. Participants’ realiza-
tion that the operators, too, might be changed was preceded by greater visual
attention allocated to the operators. Another constraint that may have made
solving Problem B particularly difficult is that the solution involves the creation of a
tautology—a statement that is true by virtue of its logical form alone. We know that
III = III = III, but it’s obvious that that is true, so we may be resistant to saying (or even
thinking?) so.
Are the processes involved in reaching a solution to this type of problem voluntary
or involuntary, controlled or automatic? After our initial explorations of various
unfruitful options, none of which yields a solution, we frequently experience a sense
of almost giving up or of not knowing where to turn—an impasse. At this point, we
know that we need to try something new or different, but not yet what.
One account of what happens at this point is that we “relax constraints” that were
implicitly or automatically adopted during our first attempts. For example, in Problem
B, the assumption that the changes must be in the values of the equation, rather than
in the operators, was relaxed, and this, for those who successfully solved the problem,
was reflected in the changed distribution of where they looked.
But where do these constraints themselves come from? A key contributor to how
we initially represent the problem involves past experience with similar kinds of prob-
lems (e.g., solving equations). When we first encounter a problem, we rely on past
general rules or ways of segmenting and understanding information (schemas, chunks,
procedures, rules) that we have used in similar situations, often successfully, in the
past. But—unlike past successes—the representation is in some manner inappro-
priate to the current problem.
Now try yet another problem (Problem Type C), again using the same rules:
Make the statement true, by moving only one matchstick.
XI = III + III
150 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
Participants who solved this problem began, toward the end of their solution attempts,
to look longer at the result (XI). Problem C can be solved by changing the result from
XI to VI, but now by decomposing the “X” itself, and rearranging it into a “V.” Problem
C requires us to overcome a different tendency—that of treating the multielement
Roman numerals (e.g., X, V) as wholes or integrated units that cannot be further
decomposed or rearranged. Again, increased perceptual attention was devoted to
the aspects that led to the solution of the problem (here the result), even before
individuals consciously were aware that this comprised the way to a solution.
The impasse in the case of Problem C arises from a different kind of nonhelpful
reliance on past experience. In this case, the solution was difficult to see because of our
tendency to treat certain well-learned or meaningful forms (e.g., X, V) in a holistic
integrated manner. This holistic processing bias makes it more difficult to think of the
possibility of breaking up or disassembling a given form into smaller component
pieces.
The processes that lead us to treat complex and well-learned objects, such as the
Roman numerals X or V, as unified “chunks” are largely automatic. Findings from
perceptual learning show that, with repetition, what was initially perceived and treated
as a complex stimulus of many individual parts (e.g., words) becomes grouped,
chunked, or “unitized” into a single complex functional unit (e.g., Goldstone, 1998).
This unit then can be perceived and rapidly acted upon, even if only a part of the
stimulus is presented.
The chunking of the multielement Roman numerals appears to be a largely auto-
matic process that occurs without much effort and without our intending to make it
happen. But what about the process of decomposing chunks when the chunks are not
necessary or when they interfere with what we need to do? Is this decomposing or
deconstruction under conscious control, or not? What is it that leads us to give up or
to relax perceptual or other assumptions that we are making that are inappropriate
and that block us from seeing the solution to a problem?
In considering their eye movement findings with the matchstick arithmetic prob-
lems, Knoblich and colleagues (1999) were reluctant to take a clear stance on this ques-
tion. For instance, in the case of the unitized Roman numerals, they suggest that,
“moving to a more fine-grained perceptual representation by breaking up familiar per-
ceptual patterns (chunks) is one of the mind’s responses to persistent failure” (Knoblich
et al., 1999, p. 1536). Yet stating that this process occurs as part of “the mind’s response
to persistent failure” describes when the constraints are changed, not how.
However, recent research provides some hints on how appropriate—but also some-
times inappropriate—constraints may exert their effects in the first place. Some
insight into the factors that lead to the adoption of what may be too narrow or other-
wise inappropriate constraints, and the factors that enable subsequent revision or
“relaxation” of those constraints, is provided by examination of how patients with
brain lesions approach the matchstick arithmetic problems. There is evidence that,
counterintuitively, individuals with lateral frontal lesions were able to solve Type C
problems not less often but more often than did normal controls. Both the patient and
control groups showed high and nearly identical levels of performance on the easier,
Type A problems. In contrast, whereas only 43% of 23 controls solved the Type C
problems, 82% of the 17 patients with lateral frontal cortical lesions did so (Reverberi,
Thinkin g wit h Ou r S e n s e s 151
Toraldo, D’Agnostini, & Skrap, 2005). Furthermore, the patients with lateral frontal
lesions solved Type A and Type C problems with equal ease.
What explanation can be given for this highly counterintuitive result? Why might
the performance of patients with brain lesions exceed that of individuals with intact
brain function on these difficult problems? Although a definitive answer to this ques-
tion is not yet possible, it is known that lateral frontal cortex is involved in a very wide
range of memory and thinking processes. The types of cognitive processes that call
on this brain region range from retrieving memory for recent events to accessing
general knowledge or semantic information, and from engaging in planning ahead
and reasoning to switching attention between tasks or stimuli. One account of what
the dorsolateral region of prefrontal cortex does in all of these quite different sorts of
tasks is to help define and select a set of possible responses that is appropriate for a
particular task and to bias responses in favor of that set.
The surprisingly good performance of the patients with lateral frontal lesions on
the Type C matchstick problems, particularly their ability to outperform the normal
controls, thus raises the possibility that our overly constrained construal of the task
may be mediated by the frontal lobes. Our too narrow interpretation may arise from
the imposition of “top-down” selection processes on perceptual and cognitive func-
tions (cf. Desimone & Duncan, 1995; Nathaniel-James & Frith, 2002).
The process of defining and selecting a possible set of responses in a given situation
has been incisively described as “sculpting the response space” by the proponents of
this account (e.g., Nathaniel-James & Frith, 2002). Damage to the lateral prefrontal
cortex is proposed to interfere with this biasing process. Paradoxically, then, the
reduced constraints on the set of possible responses in the patients with lesions to
lateral frontal cortex allowed them to solve the difficult Type C matchstick problems
more readily than did the normal controls.
Does this mean, as the authors ask in the title of the paper reporting these find-
ings, that we might be “better without (lateral) frontal cortex”? The answer clearly is
“no.” In other circumstances, and more frequently, the absence of frontally mediated
task-related constraints leads the patients to perform less well, and the absence of
such constraints may make the task more difficult. For example, although the patients
solved Type C problems more readily than did the controls, this was not true for Type
B problems, where the patients performed slightly more poorly than did the controls.
Another important measure of performance showed that there was also something
further amiss with the performance of the patients with frontal damage for the
Type B problems. This measure involved looking at the individual’s success rates not
for the first problem that was presented, but for further problems of that sort that
were presented after the first problem had been correctly solved. After a person solves
a problem of a given sort (e.g., Type B) for the first time, he or she should become
aware of the inappropriate constraint he or she had been working within and realize
that it was not appropriate. The constraint is then “relaxed.”
The researchers calculated a measure of “accuracy after relaxation” by calculating
the proportion of times a participant was able to find the solution, without cues, after
he or she had correctly solved one problem of that type before. Whereas the relax
scores for the patients and controls did not differ from one another for either the
Type A or for the Type C problems, they did differ for Type B problems. For these
152 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
problems, the controls showed significantly higher “relax scores” than did the patients.
For these problems, then, the (frontally mediated) failure to impose constraints was
clearly detrimental to the patients and they did not seem to be able to efficiently
use their prior experience with the general type of problem to help answer future
problems of a similar kind to the one they had just solved.
Adoption of excessively narrow or inappropriate constraints, and the subsequent
successful revision or “relaxation” of those constraints, may also critically involve
changes in attention and, especially, our attention to perceptual information. As
further developed in the next section, there are multiple factors that may assume part
of the blame, or a good portion of the blame, for our less than fully flexible “essays” in
approaching problems or, more broadly, intellectual and scientific puzzles of various
forms.
M A N Y PAT H WAY S TO R I G I D T H I N K I N G : N OT O N E B U T S E V E R A L
C U E S M AY L E A D U S A S T R AY
The pattern of findings with the matchstick problems seems to highlight cases where
our past learning and habits lead us to interpret and see a problem or problematic
situation in a nonhelpful way, which then leads to biased or blunted perception—a
failure to “think with our senses” (cf. Bilalic et al., 2008, 2010). Nonetheless, it is
unlikely that all of our cases of getting stuck in our thinking arise from such mis-
guided top-down (higher level) interpretations. Bottom-up processes, involving more
basic or low-level aspects of how we perceive events and objects, may also play a role.
For instance, whereas the tendency to focus on the variables of an arithmetic equation
may reflect our prior experience with mathematics, the tendency to treat individual
numerals and arithmetic operators as units rather than simply collections of straight
lines is based on our extensive experience with text and written symbols, and such
unitization may involve lower level perceptual grouping factors (e.g., Wu, Knoblich,
Wei, & Luo, 2009).
It is, then, too simplistic to assume that only one sort of factor contributes to our
impasses in attempting to solve insight problems or in our efforts to see what we
might do in other sorts of problematic situations. Although knowledge factors often
play a role, when knowledge or experiences are brought to bear on the problem that
may be inappropriate, misleading perceptual factors involving such aspects as percep-
tual integrity (e.g., unitization in the matchstick problems) and figure-ground rela-
tionships, and other Gestalt laws may conspire to make solving a problem difficult.
Such perceptually based factors may act to make us less likely to see ways that we could
get a handle on the problem, such that “crucial affordances” (Kershaw & Ohlsson,
2004, p. 4), or important entryways into handling the problem, are overlooked. Other
difficulties arise from process factors, such as how many different options can be con-
sidered and explored (e.g. Ash & Wiley, 2006; Fleck, 2008). The more possibilities
there are, the more difficult it is to be exhaustive in trying them all and to accurately
keep track of the ones we have tried. The number of steps into the future that must be
foreseen (the amount of “look ahead”) and how clearly we understand what the solu-
tion would look like, even if we should “happen upon” it (the specificity of the goal
state), are other important process factors that may cause difficulties.
Thinkin g wit h Ou r S e n s e s 153
Clear support for the idea that it may be a “conspiracy” of multiple kinds of
factors that renders some problems particularly difficult to solve was provided in an
experiment that used a different, seemingly straightforward but rarely solved, task.
Consider a simple square, comprised of nine black dots, as shown in Figure 4.4. The
problem is apparently equally straightforward: How could you connect all of the dots,
with exactly four straight lines, without lifting the pen from the paper, and without
retracing?
This apparently simple task is surprisingly difficult, such that it has an expected
average solution rate of close to 0% when presented under standard laboratory condi-
tions that allow only a few minutes for the task (Kershaw & Ohlsson, 2004; Maier,
1930). Solution rates have only rarely been raised above 50%, and this has usually
been done only by substantially changing the nature of the problem, as in simplifying
the problem by giving away the first one or two lines of the solution, by adding more
dots to the problem, or by providing extensive strategy training and practice.
Nonetheless, individual hints can boost performance to some extent. Thus, rather
than near zero, the solution rate increases to nearly 20% or 25% when participants
are given the hint that going outside the dots is permitted, and the solution rate is also
increased by placing the square on a background surface that has unfilled or shaded
circles rather than a pure white background.
Combining several hints, some of which help to “undo” perceptually based
constraints, and others that help to undo constraints based on the inappropriate
application of prior knowledge, may additively boost performance (Kershaw & Ohlsson,
2004). Participants achieved higher solution success rates if there was a background
grid that encouraged them to see that turns might be made not only on dots but also
on the surrounding background space (so-called non-dot turns) than if there was no
such grid. This change in the background helps to combat the strong figural quality of
the square formed by the dots and the mistaken assumption that the lines must be
within the figure, rather than also reaching beyond the square and changing direction
on the surrounding background. Participants also achieved higher solution success
rates if they had prior training that gave them a more specific idea of what the solution
might look like (i.e., the goal configuration). Yet neither of these types of hints led
to anything like stellar levels of performance. With a single helpful hint the highest
solution rate was only 17.5%. But combining the hints, so that a perceptual factor, a
knowledge factor, and a process factor were all simultaneously addressed, raised the
solution rate to 40%. . . . The solution is given in Figure 4.5.
154 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
This outcome, while also hardly stellar, is noticeably better than the rate obtained
with no hints or with only one type of hint. This outcome also suggests that what “it”
is that causes our failure to see (or otherwise “sense”) what’s there—or what could be
there in our endeavors at creative or insightful problem solving—is not likely to be
any one thing. Rather, “it” may most often be the convergence or unhelpful collusion
of several factors that, together, lead us into a wrong-headed and rigid approach to a
problem or situation. The rigidity of our thinking in these instances may be psycho-
logically overdetermined: an outcome of several factors, including a combination of
one or more ingredients of misleading or inappropriate knowledge application, fail-
ures to perceive, and/or factors relating to how we set about thinking about and
approaching the problem, such as a too narrowly or incorrectly defined problem.7
N OT A N E P I P H E N O M E N O N : G E S T U R E S A S R E P R E S E N TAT I O N A L
A C TO R S W I T H I N — A N D S O M E T I M E S P R E S C I E N T
P R E C U R S O R S TO — T H I N K I N G
During face-to-face conversation, individuals often spontaneously use their hands as
they talk. These “co-speech gestures,” or hand movements made concurrently during
speaking, take many different forms, but they have been broadly classified into several
types. Most prominently, such gestures include: iconic or representational gestures, in
which individuals represent action or object-related semantic content, such as bring-
ing a cupped hand to the mouth to represent “drinking”; deictic gestures, in which the
speaker indicates an object, person, or other referent that is referred to, such as point-
ing toward a building or gesturing toward a chair when inviting someone to take a
seat; and emblematic or conventional gestures, involving culturally agreed-upon signs,
such as the “thumbs-up” or “thumbs-down” signs, or raising the index finger to the
lips to indicate the need for quietness.8 Gestures may also occur during an individual’s
efforts to understand and solve problems, such as algebra or physics problems in the
case of adults, or Piagetian problems regarding the conservation of mass or liquid
(e.g., Piaget & Inhelder, 1974) in the case of children. Here gestures may be used to
represent particular aspects of the problems (such as force or diameter) or to point to
specific features of a representation or object (e.g., the origin of a graph).
Although the gestures made during attempted problem solving or the explanation
of a problem are often consistent with what an individual is saying, in some cases
an individual’s words may say one thing (e.g., suggesting that she is focused on
one aspect), whereas her gestures suggest another (e.g., suggesting awareness of
Thinkin g wit h Ou r S e n s e s 155
awareness” of the correct procedures during the pretest. Although not every child
showed the transitional pattern and not every child spontaneously used gestures,
gesture discordance was significantly predictive of concept mastery.
In addition, gesturing itself seemed to help thinking. Children who did not gesture at
all performed less well on the posttraining assessments than did children who
gestured during the task. In a further study, children who expressed a correct prob-
lem-solving strategy in both gesture and speech during instruction were significantly
more likely to correctly later solve the math problems given on a posttest than were
children who expressed the correct strategy in speech alone (Cook & Goldin-Meadow,
2006).
Although the role of gesture in thinking and problem solving has frequently been
explored in children, similar findings with adults point to instances of concordance
between the problem representations that individuals have extracted as shown in
gestures and verbal accounts, and also instances of discordance—similarly suggesting
the concurrent presence of “competing approaches” to a problem space (Alibali et al.,
1999). Undergraduates were asked to solve structurally analogous word problems in
which the problems contained entities that changed discretely, entities that changed
continuously, or included entities with both discrete and continuous changes. All of
the problems could be correctly solved using either a summing strategy, involving a
conceptualization of change as a series of discrete steps (calculating the change per
unit and then summing these amounts), or an averaging strategy, involving a concep-
tualization of change as one continuous process (finding the average rate of change
and then multiplying by the number of units). The gestures made by participants as
they worked through the problems were also classified as continuous (involving a
smooth, continuous motion such as sweeping, arcing, or dragging), discrete (involving
a set of discrete movements such as a sequence of three or more taps or points), both
continuous and discrete (e.g., a series of short sweeping motions), or neither (e.g.,
gestures that represented aspects of the problem other than manner of change).
Participants who verbally adopted a summing approach to the problem—which
involves treating change as a series of discrete events—were likely to use discrete ges-
tures; in contrast, participants who adopted an averaging approach, in which they
found an average rate of change and then multiplied it by the number of units were
more likely to use gestures that matched this construal of change as a single (continu-
ous) event. When the strategy described by the participants matched their gestures
(gesture reinforced speech), then approximately 65% of the problems were solved with
that strategy. Nonetheless, in a number of instances the aspects of the problems repre-
sented by participants by their words differed from those represented by their gestures.
It is not clear if, as in the case of children’s incipient understanding of conservation
problems or of the mathematical notion of equivalence, the presence of such speech-
gesture discordance also reflects a “transitional state” of knowledge (e.g., whether it
suggests that the individual is likely to change his or her modal problem-solving strat-
egy on subsequent problems), or perhaps whether these aspects may be more likely to
be drawn upon in future problem-solving efforts that require the generation of new
strategies (Alibali et al., 1999).9
The types and functions of gestures that occur during learning also may vary
depending on the learner’s orientation to the subject matter, particularly whether she
Thinkin g wit h Ou r S e n s e s 157
is actively “in the moment” and attempting to work through a still-not-fully under-
stood explanation, or whether she is restating an explanation that she herself has
previously worked through, or that she has been given by another. Based on a detailed
examination of the use of gestures by sixth-grade science learners, Crowder (1996)
found it necessary to differentiate between two types of gesturing, depending on the
“discourse mode” that the student was in. When the child was describing a memorized
or previously thought-out model, his gestures tended to be redundant with his speech,
and to be closely timed with it, for example, to emphasize stressed words. In this
mode, the child often looked at the listener rather than at his hands. This might be
termed a “demonstration” or “narrative description” mode. In contrast, when a child
was primarily involved in on-line thinking, actively reasoning or “running a model” in
her head, and attempting to explain “in the moment,” then her gestures were used in
a more active, integrated way, to help predict outcomes, revise explanations, and coor-
dinate components and mechanisms. In this mode, the gestures often preceded related
verbal content, foreshadowing the words rather than merely accompanying or empha-
sizing them, and often were iconic in nature to enhance meaning or elaborate upon
the spoken message. These gestures also seemed more private, rather than intended
for an audience. Crowder proposed that gestures of this active sort, during “in-the-
moment” explanation also might be internalized as mental imagery. For individuals in
the on-line thinking mode, gestures were sometimes at the forefront of thought; they
appeared to “do the work of leading the thinker toward a new level of understanding
and new ways of problem solving” (Crowder, 1996, p. 203).
How might gesture be helpful to, and in some cases be predictive of, new insights
or understanding? One proposal focuses on the visual-spatial nature of gestures, and
the better fit between expressions possible in this modality and the required under-
standing.
The visual-spatial aspect of gestures is, however, also closely interconnected with the
ability of gestures to assume a deictic or indexing function that serves to anchor the
spoken words. Gestures can help to point to relevant information, such as the objects,
spaces, and actions to which spoken language refers, and can thereby provide contex-
tual support to the spoken words.
Gesture constitutes a support system for making salient those aspects that
the talk is about, but it also is an expressive medium that enacts (in iconic
158 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
Such support includes making more salient the affordances (possibilities for action and
interaction) that objects offer. Understanding a sentence in context requires that the
listener correctly map to or “index” the referents in the sentence, either to actual objects
or events, or to perceptual or analogical symbols of those referents, and perceptual
indexing may therefore facilitate comprehension. A study by Glenberg and Robertson
(1999) provides an excellent example of the key role of perceptual indexing in promot-
ing deeper understanding. These researchers found that participants who learned about
using a compass while listening and at the same time viewing images of a compass
(termed the listen and index group) considerably outperformed a group who learned
about a compass through listening and reading (listen and read group). Even though
the two groups acquired similar levels of abstract knowledge, the listen and index group
significantly outperformed the listen and read group in actual compass reading tasks.
They read and followed new directions more quickly, they less frequently needed to
stop to refer to background information, and they used the compass and map more
accurately. To the extent that gestures serve a similar indexing function, both compre-
hension and transfer performance may be facilitated. (The indexical hypothesis is
discussed again later in this chapter in the context of “making new concepts.”)
It is also possible that, in the case of children learning the concept of mathematical
equivalence, the similarity of the gestures used to indicate equivalence across different
problems (always a sweep under one side of the equation followed by the same sweep
under the other side of the equation), helped children to focus on what was constant,
and important, across the different problems: That there were two sides to the equa-
tion, and that those two sides should be treated in the same way (Cook & Goldin-
Meadow, 2006)—setting aside the details of the individual problems.
Intriguingly, however, under some conditions, children may benefit from the
teacher’s presentation of discordant information in speech versus gesture, for example,
if the speech of a teacher focuses on one strategy, whereas his gestures highlight
a different strategy (M. A. Singer & Goldin-Meadow, 2005). Children answered more
problems correctly at posttest if the teacher, in speaking, emphasized the equalizer
aspect but, in gesture, showed how a particular type of problem might be solved
(e.g., in problems with identical addends, such as 3 + 4 + 5 = _ + 5, pointing first at the
3 and 4 together, and then the blank, while verbally emphasizing that the two sides
of the equation needed to be made equal). This observation suggests that it may be
possible to provide less obtrusive specific guidance in one representational format
(e.g., through gesture, demonstrating the grouping method for solving equality prob-
lems with identical addends) concurrently with more salient abstract guidance in
another format (e.g., through speech, emphasizing the equalizer principle). Subtly
Thinkin g wit h Ou r S e n s e s 159
gesturing toward, but not explicitly drawing attention to, a specific but not always
applicable approach to solving a problem, such as using grouping, might help a child to
discover alternative approaches without distracting from her comprehension of the
more generic principle. Thus, the potential salutary effects of gesture may in some
cases arise precisely because gesture may elude conscious monitoring:
than that found for words (e.g., Ganis, Kutas, & Sereno, 1996); this was so even in the
condition in which gesture was present but the mismatch occurred verbally.
Özyürek et al. (2007) conclude that “when understanding an utterance, the brain
does not restrict itself to language information alone, but also integrates semantic
information conveyed through other modalities, such as co-speech gestures” (p. 614),
and, similarly, “neural processing in language comprehension involves the simultane-
ous incorporation of information coming from a broader domain of cognition than
only verbal semantics” (p. 605). These findings again argue that we “think with our
senses”—in this case encompassing both the performance of manual actions and the
perception and interpretation of them.10
The different ways and contexts in which individuals may actively facilitate—and
iteratively guide, shape, and support—thinking through changing the environment
are innumerable (see, for example, Ewenstein & Whyte, 2009, and M. Wilson, 2010).
We will here consider four examples, two from the domains of leisure and sport, and
two from professional contexts, chosen to encompass multiple levels of complexity,
and differing goals and internal and external constraints.
First, what seems to be an anecdotal example but that also is supported with
experimental evidence: In the board game Scrabble, each player must generate
words containing as many letters as possible from the particular set of seven letters
that he or she has randomly drawn. The generated word must also appropriately
intersect with one or more of the words that are already placed on the board.
Experienced Scrabble players rarely simply array their set of letter tiles in a single fixed
order, and then attempt to find potential words from the one display. Instead, they
often deliberately move the letters around into different subgroups and groupings,
first creating this combination and now that combination. These movements do not
seem to be an accidental or tangential aspect of their thinking: rather, the shuffling
and shifting of letters often is undertaken precisely as a hoped-for means to stimulat-
ing new directions of thought and new possibilities, as the letters themselves associa-
tively cue candidate solutions. Players may thus be taking advantage of the physical
embodiment of the letters, knowing that they are more likely to arrive at a closer
164 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
to optimal candidate if they let the physical letters themselves do some of the
initial “work.”
Consistent with this supposition, using an experimental analog of the game,
Maglio et al. (1999) found that participants who were asked to generate as many
English words as possible (at least two letters in length, and excluding proper nouns
and acronyms) from a set of seven letters generated significantly more words when
they were allowed to use their hands to move the letter tiles than when not allowed to
do so. However, there was also a significant interaction between the hands/no hands
manipulation and letter set. Physical movement of the letter tiles was beneficial
only for one of two letter combinations that were tested (EMTGPEA), for which the
potential solutions were primarily of low written and spoken word frequency and
were relatively few in number (53 words possible); there was not a significant advan-
tage for a letter combination (RDLOSNA) for which there were more potential solu-
tions (92 words possible), and where those solutions tended to be of higher word
frequency. Thus, the benefits accrued from physically altering the order of the letters
(or more generally, objects in the environment) may be most pronounced when one
has drawn a more difficult set of letters or is encountering a more challenging task.
A somewhat more complex example of how individuals manipulate and use
epistemic objects to facilitate thinking is provided from the realm of sport psychol-
ogy—focusing on the role of physical cues in enabling effective thought in the sport of
orienteering (Eccles, 2006). In orienteering, the individual must navigate through
wild terrain as rapidly as possible, being sure to visit, in a specific order, each of many
“control points” that are indicated on a map, and that must be found and identified
through a careful reading of the map’s elevations, landmarks, and so on. Individuals
who are skilled at orienteering adopt a number of strategies to manage the multiple
challenges posed by the requirements to swiftly read the map, interpret it with regard
to their current location, while (as far as possible) continuing to run across terrain that
itself may demand considerable attention just to maintain footing and avoid hazards.
One approach is to fold the map to show only the currently relevant section of
the terrain, thereby reducing the visual search time necessary to locate the relevant
information. The map then is refolded regularly so as to maintain updated informa-
tion that is readily consulted without prolonged search for the currently relevant data.
Eccles (2006) found that all 15 of the 15 skilled participants he surveyed used this
approach; and all 6 of the 6 coaches explicitly taught this method. Map folding is
nearly always combined with “thumbing,” in which the map is carried with the thumb
indicating the individual’s current location, thereby substantially reducing the costs of
“task switching” between looking at the map and looking where one is going (14/15
participants, 6/6 coaches). Thumbing and map folding are also used together with a
continual reorienting (setting and resetting) of the map physically, so that the world
that the map represents is aligned with the actual world, thereby circumventing the
need for cognitively demanding mental rotation (15/15 participants, 6/6 coaches).
Likewise, all of the participants and coaches found a way of attaching the control card,
providing the list of “control points” that must be reached, onto the sleeve of their
arm—thereby allowing them to more readily consult it while they were running, and
facilitating rapid comparisons between the list of control points and the map. Each of
these actions: folding, thumbing, rotating, and the fixed placement of the control
Thinkin g wit h Ou r S e n s e s 165
card serves to structure the individual’s physical context to substantially aid thinking.
Other sports and leisure activities that involve multiple forms of equipment and
ongoing monitoring (e.g., sailing, mountaineering, scuba diving) may similarly benefit
from epistemic actions.
Our third example involves the ways in which (at least historically) the airline crew
of a commercial airplane determines the appropriate, and extremely critical, landing
speed for the plane (Hutchins, 1995; J. Zhang & Norman, 1994). Based on analyses of
how the cockpit crew use spoken confirmations and cross-checks, instruments, calcu-
lations, and the placement of physical objects that are also symbols (so-called speed
bugs), Hutchins (1995) argued that the memory for the speed of the airplane, includ-
ing its to-be-achieved landing speed, and needed and timely adjustments associated
with the wing configurations is not in any one individual’s consciousness. Rather, the
memory resides “in the cockpit”—as a distributed interlinked network of physical
objects and socially and cognitively interacting embodied persons. The picture of
objects as external peripheral aids to cognition that primarily proceeds “in the head”
is too simple; much thinking and much intelligent behavior arises from an interwoven
processing of internal and external information.
Let us look at one final example, one that is central to the world of intellectual, schol-
arly, and scientific pursuits, and that provides a substantive bridge to the
final section of this chapter that will focus on “words as things.” Consider the process
of writing a scholarly article. This seems to be a process that is highly (perhaps
quintessentially) dependent on processes involving internally driven thinking and
reflection—a minded gathering and spelling out and developing of arguments. But is
the thinking that leads to the final paper really quite so exclusively or predominantly
an “internal” activity? Or is the “internal” aspect only one part of a much more
complex, interactive, and iterative (“meshed”) immersion in multiple worlds? True,
there is, in the central nexus point, the internal world of the mind with its concepts
and relations between concepts, but that “mind” also is continually in intersecting
communication with external supports and guides: printed and electronic sources,
summaries, penciled notes in margins, and so on.
Taking this too exclusively internal, and too mind-and-brain-focused, construal of
the process of writing thoroughly to task, Andy Clark (2001) points to a much more
166 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
embodied and complex reality that acknowledges the heavy dependence of the
final product on “the complex ways the brain cooperates with, and leans upon, various
special features of the media and technologies with which it continually interacts.”
He continues:
We tend to think of our biological brains as the point source of the whole
final content. But if we look a little more closely what we may often find is
that the biological brain participated in some potent and iterated loops
through the cognitive technological environment. We began, perhaps, by
looking over some old notes, then turned to some original sources. As we
read, our brain generated a few fragmentary, on-the-spot responses, which
were duly stored as marks on the page, or in the margins. This cycle repeats,
pausing to loop back to the original plans and sketches, amending them in
the same fragmentary, on-the-spot fashion. This whole process of critiquing,
rearranging, streamlining and linking is deeply informed by quite specific proper-
ties of the external media, which allow the sequence of simple reactions to
become organized and grow (hopefully) into something like an argument.
The brain’s role is crucial and special. But it is not the whole story. In fact, the
true (fast and frugal!) power and beauty of the brain’s role is that it acts as a
mediating factor in a variety of complex and iterated processes which continually
loop between brain, body and technological environment. And it is this larger
system which solves the problem. […] The intelligent process just is the
spatially and temporally extended one which zig-zags between brain, body
and world. (A. Clark, 2001, p. 132)
It is not simply that we can incorporate aspects of the external world (and our own
actions) into a representational processing economy—but that we can do this quite
readily, and naturally, and are amazingly adept and amorphously versatile in the
ways that we do so, “zig-zagging” fluidly and naturally between brain, body, and world.
We are remarkably good at relying on many sorts of nonbiological epistemic devices
(pen, paper, sketchbooks, laptops, etc.) to sustain and to bolster “our prowess at
thought and reason” (A. Clark, 2005, p. 9).11
W O R D S , TO O, A R E P H Y S I C A L T H I N G S — A N D S O A R E P H Y S I C A L
A N D N OT O N LY S Y M B O L I C S H A P E R S O F T H O U G H T
Although we predominantly tend to think of words as pointers toward meanings, the
things that do the pointing are themselves physical things: Printed letters and words
are themselves objects in the world, with a particular visual shape, form, and size.
Spoken speech involves a particular series of sounds, of greater or lesser volume,
clarity, “projection,” and distinctness. Likewise, the hand, finger, and arm movements
of sign language have particular patterns and speeds of motion and direction and, for
some words, particular accompanying movements of the eyes (e.g., “sleep,” “awake”)
or facial expression (e.g., “anger,” “sad”). Words in each of these forms (printed,
spoken, signed) also necessarily inhabit a temporal space: The time between the
auditory onset of a spoken word, phrase, or sentence and its conclusion, the time
Thinkin g wit h Ou r S e n s e s 167
but also phonological neighbors of the target items—items that were not themselves
presented but that, according to the cohort activation account, may have been implic-
itly activated during the perception of the target words (Wallace, Stewart, & Malone,
1995). The prediction here is straightforward: If phonological neighbors are made
comparatively more active than are nonneighbors during speech perception, then the
earlier activation may lead participants to perceive items that are, in fact, new (not
previously presented in the experimental setting) as familiar (or more familiar than
items for which such implicit activation did not occur), in turn leading to a higher rate
of false recognition or misidentification of these items. This should be particularly
true for phonologically related words that have a relatively large window of opportu-
nity to become and remain activated, because they are consistent with the actually
presented word for a relatively long period of time. To take an example, if the target
word was domineer, a late-disqualified neighbor might be dominoes (here the phono-
logical form of the two words diverges only late in the temporal processing stream, at
the third syllable); by contrast, an early-disqualified neighbor for this same target
might be pioneer (here, the phonological form of the words diverges at the first
syllable, or very early in the temporal processing stream).
Entirely consistent with these predictions, words that were disqualified only late in
presentation as the possible word were more often falsely claimed to be recognized
than were early-disqualified lures or control words; the latter two conditions did not
differ from one another (Wallace et al., 1995). This outcome was observed using audi-
tory (rather than visual) study and test presentations of the items, perhaps arguing
for a close tie to temporal processing in inducing the effect. However, a further exper-
iment showed a similar effect even for visually presented items—though only when
each of the items was presented three times. For these repeated items, both visual and
auditory presentation elicited higher levels of false recognition for late-disqualified
items than for either early-disqualified items or control items. This led Wallace et al.
(1995) to suggest that the similarity of effects across auditory and visual presenta-
tions may have derived from recoding of the visual representations into phonological
representations, or possibly may have involved orthographic to lexical translation
(N. F. Johnson & Pugh, 1994).
Additional evidence for the initial and rapid activation of phonologically similar
words is provided by eye-tracking data. Participants who were asked to look at a dis-
play of various objects on a table (e.g., a pencil, a spoon, a bag of candy, a candle) and
were instructed to perform simple actions with them (e.g., “to pick up the candy”)
often fixated on the object that had the same initial phonemes (in this instance,
candle) before they looked at the actually designated object. Thus, their eye move-
ments showed that they were anticipating the referent of the upcoming word, and
their early predictions included objects that were phonologically congruent with the
thus-far-spoken information (Spivey-Knowlton, Tanenhaus, Eberhard, & Sedivy,
1998, cited in Spivey et al., 2005).
The phenomenon of cohort activation raises several questions: Does this occur for
all words or are there exceptions—words that have unique beginnings from the very
outset? Are there such words? How might “early unique” words differ from other
words that (as it were) announce themselves as themselves only rather less immedi-
ately and directly? To what extent do poets and other writers perhaps unwittingly,
Thinkin g wit h Ou r S e n s e s 169
N400 component, such that between 250 and 450 msec post stimulus onset,
ERPs were significantly less negative for alliterating than for nonalliterating
targets.
Although alternative interpretations of these findings are possible (for example,
they may reflect facilitated postlexical integrative processing or increased activation
for phonologically related words), Praamstra et al. (1994, p. 215) concluded that the
modulations that they observed for rhyming and alliterative words were modulations
of the same underlying component, a negativity that they deemed “similar enough to
the ‘classical’ N400 to be provisionally placed in the same category.” Furthermore, the
observation of these effects across different tasks, including those focused on the
sounds of words, as in rhyming or alliteration judgment tasks, but also under condi-
tions where participants’ goals and focus of attention were not directed toward the
sounds of the words, as in the lexical decision task requiring a judgment of whether
the stimulus is or is not a word, argues for the generality of these effects and points to
possible commonalities in how apparently formal aspects and semantic aspects of
words are processed.
More generally, these outcomes are consistent with the view that, particularly the
earlier portion of the N400 or N400m—between 200 ms and 300 ms, is “crucial for
cognitive processes at the interface of phonological and lexical-semantic analysis”
(Bonte et al., 2006, p. 121; Hagoort & Brown, 2000; also see Khateb et al., 2007).
Further elucidation of the nature of these convergences remains a promising area for
empirical and theoretical endeavors (e.g., Colombo, 1986; FitzPatrick & Indefrey,
2010; Praamstra et al., 1994) with many questions remaining. For example, do the
often facilitative effects of formal similarity sometimes, instead, lead to the opposite
outcome, with too many or too strongly activated competitors leading to decreased
rather than increased accessibility?
More broadly, heightened perceptual fluency has been found to affect several forms
of judgments (see Alter et al., 2007, for review, and for evidence that engagement in
deliberate analytical processing may be promoted by meta-cognitive experiences of
the converse subjective states of difficulty or disfluency). Fluency may affect judg-
ments of how much we like objects or words, and our preferences for one stimulus
over another. Repeatedly presented objects, which are presumably processed more
fluently, tend to be liked more and to be preferred relative to nonrepeated ones
(e.g., S. T. Murphy, Monahan, & Zajonc, 1995; Zajonc, 1968, 2001).13 Fluency also has
been shown to affect evaluations of familiarity (e.g., Whittlesea & Williams, 1998),
fame (Jacoby, Kelly, Brown, & Jascheko, 1989), and even assessments of a writer’s
intelligence (Oppenheimer, 2006). For example, participants believed the author of a
scientific abstract to be more intelligent if the abstract was written using simplified
vocabulary—and thus was more fluently read—than if the same abstract was written
using more complex vocabulary. A similar effect was found when the ease of physically
reading the words was manipulated: Participants judged the author of an essay typed
in a font that was difficult to read (italicized “Juice ITC” font) as less intelligent than
an essay typed in a more conventional font (Times New Roman).
The latter examples suggest that the illicit effects of perceptual fluency may some-
times have significant consequences and may induce biases that, if we were aware of
them, we might clearly seek to avoid. Consistent with this suggestion, if individuals
are alerted to the potential biasing effects of fluency (or of impediments to fluency),
then they may seek to counteract the effects of this factor on their judgment. However,
this is not an easy task, as calibrating the level of adjustment needed may prove diffi-
cult, so that individuals may either undercorrect for the bias or overcorrect for it (see
T. D. Wilson & Brekke, 1994). For instance, in a further experiment, Oppenheimer
(2006) found that participants’ ratings of the intelligence of a graduate school appli-
cant, and their decisions as to whether they would or would not recommend accepting
the applicant, were positively biased if the page on which the applicant’s statement
appeared was difficult to read because it was printed using a laser printer with a low
toner cartridge. Here, participants were likely to be very aware of the difficulty they
were experiencing in attempting to read the text. However, because they were both
aware of the impediment to fluent reading, and could identify a salient cause (low
toner) for that lack of fluency, they did not “penalize” the applicant for that lack of
fluency. Indeed, participants who read the application in low toner font overcompen-
sated for this perceptual effect: They rated the applicant as significantly more intelli-
gent than did participants who read the same application printed in normal font
(Cohen’s effect size d = 1.09), and they were significantly more likely to recommend
acceptance than were the normal font readers (Cohen’s effect size d = 0.86).
Enhanced fluency also may arise from only partial repetition, as in rhymes, or
alliteration. A particularly clear demonstration of the inadvertent “leaky” effects of
fluent perceptual processing on higher level judgments, in this case arising from the
poetic features of language, is provided by a study by McGlone and Tofighbakhsh
(2000; see also Häfner & Stapel, 2010). Participants were asked to evaluate unfamiliar
aphorisms for how accurately they described human behavior. Their evaluations were
contrasted for aphorisms that rhymed (e.g., Woes unite foes; What sobriety conceals,
alcohol reveals) versus nonrhyming paraphrases of the rhymes (e.g., Woes unite enemies;
172 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
What sobriety conceals, alcohol unmasks). Each aphorism was presented in one form
only for a given participant, but both forms were given across participants. If partici-
pants were not explicitly cautioned as to the need to distinguish between the contents
of the aphorism and its poetic qualities, then they gave significantly higher accuracy
ratings to the original (rhyming) aphorisms than to the modified (nonrhyming)
aphorisms. However, if explicitly cautioned to base their accuracy judgments “only on
the claim that the statement makes about behavior, not the poetic quality of the state-
ment’s wording,” then participant’s evaluations of the rhyming aphorisms were
significantly lower in the warned than in the nonwarned (control) condition, and,
also, in the warned condition, there was no difference in the accuracy judgments for
rhyming versus nonrhyming statements.
Providing individuals with a warning enabled them to circumvent the tendency,
shown by the control participants, to “conflate fluency with perceived accuracy”
(McGlone & Tofighbakhsh, 2000, p. 426). Yet this difference in susceptibility to the
differential effects of rhyming versus nonrhyming prose did not arise from differences
in individuals’ explicit beliefs about the relevance of literary form to truth content.
When asked at the end of the experiment, “In your opinion, do aphorisms that rhyme
describe human behavior more accurately than those that do not rhyme?” all of the
participants, regardless of condition, appropriately and unsurprisingly enough,
answered “no.”
These outcomes thus show that the physical character of text or words (here rhym-
ing phrases that were read silently by participants) can exert a substantial and in some
cases unintended and unwanted effect on higher level evaluative processes. These
findings further show, however, that under some circumstances, paying more explicit
attention to words as physical objects, and the distinction between words as concrete
objects in the world and their referents, can bolster resistance to illicit effects of words
as things on our further cognitive and evaluative processes.
Additional evidence suggests that the unintended “overreaching” effects of fluent
processing may not be limited to the easily identified, salient aspects of words, such as
rhyme—and also may extend to other sorts of evaluations, including assessments of
the importance of medical research or other findings (Labroo et al., 2009), and finan-
cial decisions (e.g., Alter & Oppenheimer, 2006). In both a laboratory simulation and
in two analyses of naturalistic real-world stock market data, Alter and Oppenheimer
(2006) found that fluently named stocks robustly outperformed stocks that were
relatively more difficult to name. In the laboratory study, fabricated stocks were
independently rated for the ease with which their names could be pronounced by one
group of participants and another group estimated the performance of those stocks.
Fluently named stocks were rated as likely to increase in value over a year of trading
(mean expected value significantly above zero, showing appreciation), whereas
nonfluently named items were expected to show devaluation (mean expected value
significantly below zero).
Two naturalistic real-world studies, using stocks that were newly released on to
the market, and for which, therefore, individuals were unlikely to have a great
deal of diagnostic information concerning the likely performance of the company,
showed a similar outcome. In one study, newly entering companies on the New York
Stock Exchange that were rated as having highly pronounceable names showed
Thinkin g wit h Ou r S e n s e s 173
a significantly larger percentage change in share price on the first day and the first
week of trading than did newly entering companies with less pronounceable names.
This effect persisted, in nonsignificant attenuated form, at 6 months and 1 year. This
“fluency effect” was further supported and extended in a second study, involving both
the New York Stock Exchange and the American Stock Exchange, that examined the
effects of the company’s three-letter stock ticker identification code as a predictor of
performance. Companies that had a pronounceable ticker code (e.g., KAR) outper-
formed those with a nonpronounceable code (e.g., RDO) on the first day of trading;
this effect became attenuated and was not significant beyond the first day.
These studies convincingly demonstrate that there are many, often uninvited and
unlooked for, effects of the physical features of words and phrases on higher level
judgment. These instances, here taking a nondesirable rather than desirable form,
nonetheless also demonstrate the degree to which we do, indeed, “think with our
senses.” Not only our cognitive and evaluative judgments but also our actions may be
partially guided by inferences driven by “sensory-perceptual fluency.” Very concrete
(low-level) changes in the ease with which we identify and perceive words and text are
not to be ignored, and they may have considerable (sometimes unwelcome) conse-
quences.
Looking Back
This chapter has marshaled together, and asked us to reflect on, the many—
sometimes hidden or overlooked—roles of sensory-perceptual and motor informa-
tion in enabling complex thought and reasoning. Particular (specific) sensory-perceptual
and motor information has been shown to play an essential part in several forms
of complex thought. Among the complex modes of thought that we have considered,
each of which we found recruited (or was subserved by) the representation of
particular sensory, motor, and kinesthetic properties of objects are: The generation
of new hypotheses and the ampliative form of reasoning known as abduction; the
apt and ready access to a solution to a problem in one situation based on the
earlier use of an analogically similar solution in a very different context; the incipient
and later consummate mastery of abstract concepts such as the mathematical
notion of equivalence; and the innovative creation and rapid understanding of
entirely new uses of language in our “on-the-fly” context-appropriate “making of new
concepts”.
From the perspective of the iCASA framework, this chapter primarily provides
evidence for the importance of multiple levels of specificity in agile thinking. It is from
within the richly intertwined and intermixed use of representations at multiple
levels of specificity that innovative and generative thinking occurs. However, notable
support for the dual role of both controlled and automatic processes in adaptively
flexible thinking also emerged.
Support for the latter was found, for example, in the notions that gesture and
perhaps also eye movements may provide an implicit source of support for our
reasoning and thought processes through their deictic or indexing function. We saw
that our own gestures, or the gestures of others, may be rapidly and seamlessly
174 M E M O R Y , C AT E G O R I Z AT I O N , A N D C O N C E P T S
integrated with more purely “linguistic” meaning in a single unification space, and
that such gestures can presage conceptualizations that have not yet been fully spelled
out in an explicit, conscious, and controlled way. Additional support derived from
observations of the ways in which gesture may increase working memory capacity:
“embodied” physical actions such as pointing or gesturing may supplement and extend
cognitive resources. Given the central role of cognitive capacity (e.g., working memory
capacity) in enabling fluid, on-the-spot reasoning, and in such ubiquitous cognitive
processes as managing interference and keeping track of goals and subgoals, gesturing
thus comprises an important avenue for the influx from perception and action into
the “heart of thinking”.
Similarly, with regard to the external world of physical objects, we saw that multi-
ple large and small physical adjustments of the spaces in which we work and play, such
as how we carry and fold and hold a map, may help us to meet at least some task
demands “in the world,” rather than only “in our heads.” What we might characterize
as a “thoughtful external world,” or one that is aptly arranged to most readily meet our
goals, can set free more of our internal mental and self-regulatory resources for those
challenges that are less amenable to direct action, either immediate or further in the
future. Aptly arranging the external world can enable us to more adeptly continue on
our way, zigzagging between mind, body, and world, in an interlinked intermeshed
representational space that continues to grow and change with our aims and our
progress toward them.
The many sorts of impetus and motivations for such progress in enabling agility
of mind are the topic of our next chapter. The next chapter also brings us from
Part I, where we have focused on memory, categorization, and concepts, to Part II,
focused on motivation and emotion. Like Part I, Part II is comprised of three chapters:
Chapter 5 focuses on action and motivation, and Chapter 6 on emotion, self, and
personality. The last chapter of Part II (Chapter 7), entitled “Thoughts about Thoughts:
The Control versus Noncontrol of Thinking,” revisits and extends several themes we
will have explored in all of the chapters until then, particularly focusing on the ways in
which our thinking is a function of complex conjoined cognitive, motivational, and
emotional factors, such as our beliefs about the nature of learning and our tolerance
for uncertainty versus ambiguity.
We might begin thus: Why would someone want and take a single boot, rather than
a pair of boots? Why might one not be contented with a single new boot and return to
fetch an old one? Unless (an unlikely starting point) the person had only one foot or
the use of one foot, it is unlikely that a single boot would be taken to wear and, ordi-
narily, a new boot would be preferred to an old one (of the same size). Ordinarily,
unless there is something distinctive about an old one that is untrue of a new one.
They differ in their visual appearance, and their texture, and . . . ah, yes, an old boot
will be securely inhabited by the familiar smell of its longtime owner, whereas this
would not be so of a very new one. But why would the smell of a boot matter? What if
the boot was taken precisely for its smell? To allow a dog—a real dog, a real hound, to
get the scent of its owner? But there it is! What we have to deal with may not be
a long-known, often-told ghostly and ghastly legend of a dog, a dog that is no more,
but rather an all too real and still living one!
lines, each terminating in a sudden (sharp and jagged) point, whereas the letter
m moves flowingly forward, returning to anchor itself, to be sure, on the solid founda-
tion of the line, but then moving ahead, as though tracing the graceful arc of a
bridge—and itself forming a bridge, a bridge to effortless, pleasant, productive
thought and writing.
Simulating not the sensory-motor movements of writing, but the sounds
associated with the letter m, hearing oneself say, mm, or feeling oneself saying it: this
is likewise a soft flowing easy humming. Sometimes we hum to signal a beginning—to
begin a beginning. Prolonging or extending the sound, making it last and spanning
moments, or pausing and then repeating it, bespeaks something that is pleasurable, to
be delighted in: mmm mmmmm mmmmmm. . .
Part Two
It would become me
As well as it does you, and I should do it
With much more ease, for my good will is to it,
And yours it is against.
—William Shakespeare (1623/2006, The Tempest III.i.28–31)
In this chapter, we further broaden the scope of our window into agile thinking beyond
that of the representational world of memory, categorization, and concepts (the focus
of Chapters 2 and 3), and beyond that of sensory-perceptual and motor inputs and
guides to representations and thinking (the topic of Chapter 4), to encompass action
and motivation, or the impetus for, and enactment of, agile thinking. The chapter consists
of four main sections, each of which, in turn, is comprised of several subsections. The
four sections focus on, respectively: (a) hierarchical models of action control and
motivation, particularly in relation to higher level versus lower level construals of our
actions, and the interactions between controlled and automatic processing in forming
and implementing intentions; (b) the need for moderate and changing levels of
control, emphasizing the correlation of moderate levels of control with increased
resiliency and the growing evidence that executive control or self-regulatory processes
may, under some conditions, become depleted if the need for high levels of self-
regulatory control is sustained for prolonged periods; (c) forms of motivation and
incentives, especially evidence that contests the often proposed conflict between
intrinsic and extrinsic motivation, and that underscores the important synergistic
effects that may be obtained by a combination of intrinsic and extrinsic motivational
orientation; and (d) the potential powerful role of reinforcement in encouraging
organisms not only to repeat but also to vary, including in innovatively creative ways.
Thus, further developing the iCASA framework, we here focus on alterations in our
level of representational specificity, and our level of control, with regard to actions and
our motivation for action, in enabling mental agility.
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180 M O T I VAT I O N A N D E M O T I O N
of the groups were told that it was quite likely that the signal light would blink at
various times during their speech, and that therefore they should try to remain mind-
ful of their voice throughout the speech (low-level action identification manipulation).
The other half were told that it was unlikely that the signal light would blink during
their speech and that they should concentrate on being persuasive in delivering the
speech (high-level action identification). Whereas the light did blink 10 times during
the speech for those in the former group, it never blinked during the speech of the
latter group.
Although one might think that the blinking light would disrupt performance for
everyone, the actual effects depended on whether the participants were in the “easy”
task (addressing a purported audience that would be easy to persuade) or the
“difficult” task (addressing a skeptical, difficult-to-persuade audience). Speech dysflu-
encies (e.g., “ums,” stuttering, and long pauses, as evaluated by independent raters of
the videotapes) were highest in the two conditions in which there was a mismatch
between the perceived task difficulty and the level of action identification: that is, the
easy task together with a low level of identification, or the difficult task together
with a high level of action identification. Speech errors were less frequent in the two
conditions in which there was a match between difficulty and level of identification
(easy task + high level identification, or difficult task + low level identification). Similar
crossover effects—such that conceiving their actions at a low level of action identity
boosted participants’ performance on the more difficult task but impeded it on the
easier task—also were observed on the participants’ self-ratings of their performance.
For instance, compared to the other conditions, participants were less anxious and
less dissatisfied with their performance in the matching conditions (easy task + high
level identification, difficult task + low level identification).
These outcomes are a strong example of the need for an optimal match between the
level of specificity at which we construe our activities and the difficulty of the task:
More abstract identifications may be most beneficial for tasks that do not require
step-by-step careful monitoring of the specifics of our activity (or do not require it
under a given set of conditions), whereas more concrete identifications are most
helpful for difficult tasks. Using terms that were suggested by Vallacher and colleagues
(1989), a mismatch may involve either “identity inflation” (the activity is personally
difficult but one is thinking of it, nonoptimally, in overly broad terms that cannot
guide the action) or “identity fragmentation” (the activity is personally easy or
well practiced but one is thinking of it, nonoptimally, in overly concrete low level
terms).
Our optimal and most agile and adaptive functioning may occur when we fall victim
to neither identity inflation nor to identity fragmentation. Nonetheless, the content
of our action identifications is also important, and “higher level” identifications may
lead to difficulties if they make undesired habitual actions more resistant to change.
Thus, differing levels of action identification also may play a role in problematic habit-
ual behaviors, such as alcoholism. For instance, whereas “having a drink” is a particu-
lar short segment of action, more abstract construals of drinking such as “relieving
tension” or “rewarding myself” may take longer to achieve, and so may result in longer
stretches of behavior that are resistant to interruption or alteration. “Identifying
the action at high levels, then, may make the action more stable, precluding for the
182 M O T I VAT I O N A N D E M O T I O N
duration of the action any attempts to regulate its performance” (Wegner et al.,
1989, p. 201).
To examine whether how individuals identified their behavior did tend to change
to higher levels as behaviors became more habitual, Wegner et al. (1989) asked four
groups of individuals to rate how well various descriptions fit the act of “drinking
alcoholic beverages.” The groups included students who reported low, moderate, or
heavy alcohol use, and clients who were in an alcohol treatment center. Individuals in
the alcohol treatment center and heavy alcohol use students endorsed significantly
fewer low-level descriptors of the act of drinking alcoholic beverages than did either
low-use or moderate-use students. The heavy-use and alcohol treatment clients also
endorsed more high level descriptors, though the particular descriptors endorsed
sometimes differed. For example, both heavy-use students and alcohol treatment
clients characterized drinking as “relieving tension” significantly more often than did
low-use students. However, the alcohol treatment clients endorsed “hurting myself”
more often than did any of the other groups, including the heavy-use students, and
they significantly less often characterized drinking as “rewarding myself” than did the
heavy-use students. These findings show both differences in the predominant level of
action identification as a function of experience in a domain (more frequent drinkers
endorsed more high-level characterizations of their drinking behavior), and that such
high-level characterizations, although they have the potential to be adaptively useful,
also may (under some circumstances) lead to obdurate resistance to behavioral change
that is detrimental to an individual’s well-being.
More recently, level of action identification also was implicated in the severity of a
quite different form of habitual action: that of obsessive-compulsive hand washing
(Dar & Katz, 2005). Obsessive-compulsive disorder patients who engaged in compul-
sive hand washing were asked to rate their degree of agreement with several descrip-
tors of hand washing that reflected either a low level of identification, relating to its
technical and concrete aspects (e.g., “I soap my hands,” “I turn on the faucet”) or a com-
paratively higher level of identification, concerning its purpose or meaning (e.g., “I feel
cleansed,” “I am doing the right thing”). Obsessive-compulsive patients agreed more
with high level descriptors and less with low-level descriptors than did matched control
participants. Furthermore, the endorsement of high level rather than low-level descrip-
tors of the action of hand washing was strongly related to the severity of the disorder.
On the one hand, the latter findings appear to contradict a salient characteristic of
obsessive-compulsive behaviors. Obsessive-compulsive patients often are extremely
and minutely focused on the details of their compulsive behavior yet, particularly for
individuals experiencing a severe disorder, they seldom endorsed items that described
the concrete technical aspects of the behavior. On the other hand, this apparent para-
dox may arise from the aims with which the obsessive-compulsive individual engages
in detailed and careful instantiation of hand washing. Rather than “ends in them-
selves” the detailed and careful steps are a means to achieving certain emotional and
internal states, such as “calming myself” and “overcoming nagging thoughts”:
The details of the act are not dictated by the need to achieve a normal level of
cleanliness, but rather by the desire to achieve a specific internal state, such
as a feeling of confidence or comfort or an alleviation of anxiety or disgust.
Act ion an d M ot iv at ion 183
The increased stability of actions arising from comparatively higher level action
identification is, in these two examples, detrimental, because it is helping to maintain
habitual behavior that is ultimately undesired. Yet the flip side of this is that, in
situations in which a behavior is desired, higher level identifications of “what we are
doing” may help to preserve action in the face of obstacles—and to make us resistant to
the intrusion or “infiltration” of goals from other sources:
C O N S T R UA L T H E O R Y, M OT I VAT I O N , A N D S E L F - R E G U L AT I O N
In Chapter 3, we considered evidence that the level of construal that an individual
adopts may affect the basic cognitive process of categorization. For instance, we saw
that individuals who were asked to imagine a temporally near event, associated with a
more concrete construal level, grouped and classified objects relating to that event
into significantly more categories (i.e., more numerous, narrower, and concrete units)
than did individuals asked to imagine a temporally distant event, who used fewer,
broader, and more abstract units (Liberman, Sagristano, & Trope, 2002; for a replica-
tion and extension see also Wyer, Perfect, & Pahl, 2010, Study 2).
Construal level may also be altered by differentially focusing attention on the
methods to be used in accomplishing a goal (how), rather than the reasons for the goal
(why). These changes in construal level may then alter further motivational aspects,
such as the saliency or accessibility of different goals, both for oneself and for others.
In one study, participants who were repeatedly asked to consider why they should
improve their health or their academic performance (a task orientation that focuses on
increasingly abstract, longer range, and more encompassing goals, values, and aspira-
tions) expected that others would, and recommended that others should, seek to obtain
more accurate but potentially self-threatening weakness-focused feedback regarding
their social intelligence or career selections than did participants who were repeatedly
asked to consider how they should improve in these domains (Freitas, Gollwitzer, &
Trope, 2004). The latter task orientation led to a focus on specific, concrete actions and
stimuli and this focus, in turn, increased the relative weighting participants appeared
to give to considerations of the immediate present. These participants thus expected
(and recommended) that others should avoid the discomfort that is likely to be
provoked by receiving self-threatening weakness-focused feedback.
In contrast, the abstract-mindset group judged that others’ long-range goals would
be more salient and more strongly affected by the feedback than did the concrete-
mindset group. The abstract-mindset group also more often referred to goals relating
to self-knowledge than did the concrete-mindset group. This study has several striking
parallels to the process of “self-affirmation” that is discussed in the second section
of Chapter 6; as noted there, it has been found that self-affirmation leads participants
to prefer, on average, a higher level of action identification for several everyday
behaviors, such as “making a list” or “reading.”
In the preceding studies, participants were encouraged to either think about
how, or why, they accomplish certain goals, and this led to changes in the relative
accessibility of different types of motivational considerations. Largely parallel shifts
in the relative accessibility of information may occur when we move from a more
Act ion an d M ot iv at ion 185
deliberative mindset before making a decision to act or not to act in a certain way,
when we are still in the midst of weighing the pros and cons and other considerations,
to the state of having already made a decision (e.g., Gollwitzer, 1999; Gollwitzer et al.,
1990). Individuals who have already decided upon a goal or intention become focused
on how to accomplish the goal. Once in this implementation (rather than deliberative)
mindset, we may become especially attuned to the factors that are relevant to the
action, and we may adopt a positively biased view of the “situational affordances” for
accomplishing the hoped-for goal (Gollwitzer & Kinney, 1989; S. E. Taylor & Gollwitzer,
1995). A further important difference between deliberative versus implementation
intentions concerns the extent to which the two types of intentions can draw upon
more automatic processes. As will be seen in the following section, forming highly
specific implementation intentions for future intended actions can substantially
increase the likelihood that a given intention will be actually carried out, in part
by transferring the cuing of action initiation to less demanding automatic cognitive
processes.
As with levels of action identification, where it is neither uniformly beneficial to
adopt a high-level construal or a low-level construal, there are both benefits and
costs associated with deliberative versus implemental mindsets. Awareness of the
differential manner in which these mindsets may filter our thinking and our aware-
ness of problem-relevant information, and bias us toward focusing on relatively
lower level (more concrete) versus higher level (more abstract) factors, may help to
attenuate an excessive movement in either of these directions and thereby increase
agile thinking. Consideration of these very broad effects of mindsets on our thinking
also suggests that it may be beneficial to deliberately plan for (or even require) periods
of deliberative reevaluation during the course of larger scale projects, perhaps at more
natural “choice points” in the development of a project, at which the explicit aim is not
to implement further steps, but to reevaluate and if necessary reorient and rethink
planned directions. Stepping out of our action-oriented implementation mode during
such reevaluation phases of a project may enable shifts in mental construal level that,
in turn, allow the timely identification of newly emergent “bigger picture” threats, or
opportunities.
F L E X I B LY P O S T P O N I N G A N D R E S U M I N G I N T E N T I O N S :
LEVELS OF SPECIFICITY IN REMEMBERING
AND ACTING ON INTENTIONS
Many of our intentions or goals cannot be acted upon immediately but, instead,
require that certain conditions that are not currently in place first be met (e.g.,
particular materials or persons must be available or, often, a complex conjunction of
time, place, and persons or objects must occur). Adaptive thinking and action thus
often turns on our ability to recognize that an opportunity to fulfill an “open goal”
exists and is now at hand.
When a goal needs to be postponed, it may be particularly useful to explicitly bring
to mind specific aspects or features of the sort of situation that would, in the future,
provide a good opportunity for the realization or resumption of the goal. To take a
commonplace example: If you need to purchase olive oil, but satisfactory olive oil is
186 M O T I VAT I O N A N D E M O T I O N
not available in the grocery shop where you usually go, you might make a mental
note that the next time you purchase cheese or olives at the delicatessen, you also
should look for olive oil there (a highly specific feature-based and location-based cue).
This strategy, which Seifert and Patalano (2001) have described as “predictive encod-
ing of pending goals,”2 may enable us to better recognize opportunities for goal
completion when they arise.
Specific cues, rather than more general ones, have been shown to increase the
likelihood that we will successfully identify opportunities for the realization of
pending goals (a form of prospective memory for intentions). For example, in a brief
opinion survey, participants who were asked to perform a particular task after com-
pleting the survey were more likely to remember to do the task if they were asked to
do so after they had finished a specific sort of question (“the Black Panthers question”)
than after they had finished a more abstractly described behavior (“the last survey
question”) (Loftus, 1971). Similarly, other research has shown that participants were
more likely to successfully remember their intention to perform a given task when
they have been prompted to take note of and remember each of the particular instances
when the task should be performed. Intention completion was greater if participants
mentally prepared themselves to perform the intention in response to the occurrence
of any one of the specific words, “lion,” “leopard,” or “tiger,” that might appear on the
computer screen during another task that they were doing than when they were asked
to remember to perform the intended task whenever they encountered any instance
of the more general category “animals” (Einstein, McDaniel, Richardson, Guynn, &
Cunfer, 1995; also see Ellis & Milne, 1996). Both younger and older adults showed
enhanced recognition of the opportunities for goal fulfillment when given specific
prospective memory cues compared to more general cues, and the magnitude of the
enhancement was similar for the two age groups.
One of the reasons for this pattern of outcomes may be that a highly general
or “superordinate” category term such as “food” tends to spontaneously lead one
to think of many different sorts of items that might be described by that category
(e.g., meats, vegetables, fruits, cereals). However, if the potential occasions for
performing the intended task are drawn from a more limited range of events, then
one’s attention and memory would not be ideally focused to identify opportunities
for completion of the pending goals. Findings from a research study by Ellis and Milne
(1996), in which they used a third, and intermediate level of specificity as the cue,
supported this possibility. They found, as in other research, that there was a strong
advantage for highly specific prospective cues (e.g., “bananas,” “pears,” “apples,”
“oranges”) compared to the very general or abstract superordinate category cue (“food
items”). However, there was only a weak advantage for participants who were given
the highly specific cues compared to a group who were told to remember to perform
a given action whenever they encountered any “fruits” (a narrower subordinate
category than “food items” but not as highly specific as actually listing all possible
exemplars of that subcategory).
This latter finding is important because often we may not be able to anticipate
exactly which situations might arise that will give us the opportunity to fulfill an
intention or an open goal. Nonetheless, we should attempt to deliberately bring
to mind possible kinds of opportunities that may arise. Flexible resumption of
Act ion an d M ot iv at ion 187
increased emphasis on the need for performing the prospective task shifted
participants away from reliance on spontaneous reminding to deliberately controlled
monitoring, even though this did not always enhance performance on the prospective
task. Costs to the ongoing task were also observed when there were several possible
cues that needed to be responded to, rather than only one, and when the cues for the
prospective task were likely not in “focal” awareness (e.g., rather than a word, the cue
was comprised of only one syllable, such as “tor,” when the ongoing task required
monitoring of the semantic content of words to make classification judgments).
Additional evidence for automatically cued reminding was provided by a condition
in which an earlier prospective memory cue was made irrelevant by suspending
the requirement to perform the prospective memory task. Nonetheless, presentation
of the no-longer-relevant cue during the task resulted in a trial-specific slowdown on
a different (lexical decision) task. This suggests that automatic and “obligatory” recog-
nition of the cue’s prior relevance sometimes occurred even when the cue was
irrelevant to (and here was detrimental to) the performance of the task that was now
at hand.
Anticipating potential contexts in which we might act to fulfill open goals by imag-
ining and linking an intended action with a specific environmental situation (“when
situation x arises, I will perform y”) may enable us to switch from relying on effortful
and demanding conscious and deliberate attempts at remembering to allowing our
memory to be automatically cued by the eliciting events (Gollwitzer, 1999; Gollwitzer
& Brandstätter, 1997). Forming a detailed implementation intention, with informa-
tion about how, when, and where one will complete a desired action (e.g., a deadline
for completing a given project), and then imaginatively rehearsing this particular situ-
ation, may later enable the automatic triggering of the desired action, without the
need for further rehearsal or demanding cognitive control strategies (Gollwitzer,
1999; Gollwitzer & Brandstätter, 1997; Gollwitzer & Schaal, 1998). Very aptly, this
process has been termed “strategic automatization” by Gollwitzer and Schaal (1998;
see also I. S. Gallo et al., 2009).
Notably, there is evidence that forming implementation intentions (essentially
prospective if-then rules) increases an individual’s perceptual sensitivity to cues
relevant to the intention even for highly habitual stimuli and for which detection of
the relevant cue is difficult (T. L. Webb & Sheeran, 2004—detecting occurrences of the
letter f in a passage, when this is difficult to do for “function” words such as “of”).
Furthermore, this enhanced sensitivity does not appear to lead to an increased number
of false alarms (mistakenly classifying situations or stimuli as intention-relevant
when they are not), and it also does not lead to slower responding to ambiguous
stimuli (T. L. Webb & Sheeran, 2004). Forming specific implementation intentions
has been found to effectively promote intended actions in a wide variety of contexts,
both for actions that occur only once and for actions that need to be performed repeat-
edly such as health- and safety-related behaviors (Sheeran & Orbell, 2000; Sheeran &
Silverman, 2003; also see Koestner, Lekes, Powers, & Chicoine, 2002).
Developing specific implementation intentions may be a powerful means to coun-
teract the pull of a well-established habit, placing a different mode of “automaticity”
against a habitually cued goal or behavior, to decrease the likelihood that the new
intention is derailed by the older habitual response. This approach may also lead to
Act ion an d M ot iv at ion 189
improved memory for intentions in individuals who may experience difficulties with
deliberate conscious remembering, but not with relatively automatic forms of
processing, such as some older adults (e.g., Chasteen, Park, & Schwartz, 2001; Jacoby,
Jennings, & Hay, 1996). Older individuals who were given guidance in how to use such
“implementation intentions” showed improved prospective memory in a realistic
glucose monitoring task relative to controls who merely repeatedly rehearsed the times
that they were to take the glucose readings, or individuals who were asked to deliberate
concerning the pros and cons of testing their sugar level (Liu & Park, 2004).
The potential interplay between automatically cued and strategic monitoring for
opportunities to fulfill open goals or intentions is also clearly demonstrated by the
finding that individuals with brain lesions to the frontal lobe—who often experience
clear difficulties in appropriately executing effortful, deliberate, and strategically
demanding tasks—can nonetheless benefit from such an approach of detailed
implementation intention formation (Lengfelder & Gollwitzer, 2001). Patients with
frontal lobe lesions, patients with nonfrontal lesions, and two nonclinical control
groups were asked to track a moving circle across a computer screen and also, at the
same time, to monitor for any appearance of a number in the center of the moving
circle. They were asked to press a mouse button as quickly as possible to any numbers
that appeared, but to try to respond especially quickly to any occurrences of the
number 3. If, however, any letters appeared, they were to withhold responding. This
created a go/no-go situation, with critical targets (the number 3), noncritical targets
(the numbers 1, 5, 7, and 9) and distractor items to which the individual was not to
respond (the letters a, e, n, v, and x). Although patients with frontal and nonfrontal
lesions were slower in responding overall, all groups responded significantly more
rapidly to appearances of the critical target if they had formed an implementation
intention beforehand. That is, participants who explicitly thought, “If the number 3
appears, I will press the button particularly fast!” responded more quickly to critical
targets than did participants who took part in a familiarization phase that controlled
for experimenter expectancy and the repeated presentation of the target item but did
not encourage the formation of a detailed implementation intention. The advantage
for the implementation intention was similar in the frontal lesion group compared
with the control groups and the nonfrontal lesion group.
Furthermore, when all of the patients were separated into two groups, based on
their performance on a difficult deliberate planning task (the Tower of Hanoi task,
requiring the movement of disks across a number of pegs in accordance with several
rules, such as that no disk may be placed on another disk that is smaller than itself), it
was found that those patients who showed relatively more impaired performance on
this controlled planning task benefited the most from forming the implementation
intention. That is, these patients showed the greatest speedup for the critical target
trials. Notably, the patients with lower deliberate planning scores also outperformed
university students for these conditions.
A clear implication of these findings is that the tendency of individuals with frontal
lobe lesions, and also of other patients such as some persons with traumatic brain
injury, to be overly guided by habitual or automatic responses to environmental
cues—under the right conditions—may actually be used to help them. Specific condi-
tion-to-action cues could, for instance, be used to help individuals to improve their
190 M O T I VAT I O N A N D E M O T I O N
daily planning abilities and initiation (cf. Cicerone, Levine, Malec, Stuss, & Whyte,
2006). Additionally, these findings suggest that, in healthy individuals, even under
conditions designed to encourage the operation of automatic responding, intact reflec-
tive and deliberative monitoring abilities may to some extent continue to modulate
and partially dampen such responding. Nonetheless, forming more specific imple-
mentation intentions may increase the likelihood of successful goal completion.
One final study investigating the effectiveness of implementation intentions also
provides a clear cross-connection to the next section concerning broader motivational
aspects of self-control. Consistent with the construal of implementation intentions as
a form of “strategic automatization,” Webb and Sheeran (2003) found that the forma-
tion of implementation intentions helped to attenuate the detrimental “depleting
effects” on self-control capacity that can arise from a prior effortful attempt at
self-regulation. Stated differently, implementation intentions seemed to “conserve”
effortful processing capacity. In one study, all participants first were given the Stroop
color-words task, which requires individuals to name the ink color of printed words
and to ignore the referents of the words that also comprise the names of colors. After
finishing the Stroop task, they were asked to attempt to solve a difficult (impossible)
puzzle task. However, participants in the “implementation intention” condition were
asked to tell themselves how they would respond to the words on the Stroop test, such
as “as soon as I see a word I will ignore its meaning.” This implementation intention
group persisted significantly longer in trying to solve the puzzle task than did partici-
pants who did not form implementation intentions. A further study showed that
even if participants had already completed a demanding self-control task, forming
implementation intentions for how to perform the Stroop task “protected” perfor-
mance on that task. Those who performed the Stroop task following the demanding
self-control task but under implementation intentions made significantly fewer
errors, and also named the ink colors significantly more rapidly, than did those who
performed the task without such intentions.
The ego-resilient individual could shift behaviors, had available a versatile set
of cognitive and social procedures in the search for adaptation, could both
assimilate and accommodate, was deliberative but not ruminative, was quick
192 M O T I VAT I O N A N D E M O T I O N
to adapt, was able to plan and work for a distant goal, and was also able
to relax and relish enjoyment when circumstances suggested and permitted.
The relatively unresilient or vulnerable individual displayed little adaptive
flexibility, was disquieted by the new and altered, was perseverative or diffuse
in responding to the changed or strange, was made anxious by competing
demands, and had difficulty in recouping from the traumatic. (J. Block &
J. H. Block, 2006, p. 318)
intelligent females. Letzring and colleagues (2005) note that, although this seems to
be opposed to the notion that higher levels of control are associated with greater
cognitive skill and are therefore always advantageous (i.e., the notion that greater con-
trol is “monotonically advantageous,” discussed at length later), this apparent discrep-
ancy may reflect differences in the level of control that is typically assessed. In
particular, whereas many investigators focus on the range between too little control
and appropriate control, fewer investigators focus on the range between appropriate
control and too much (over) control. However, in this context it is also noteworthy
that J. Block and J. H. Block (2006) found that whereas for the boys and young men
that they studied, there was almost no correlation between ego control and ego resil-
iency over time, for girls the pattern changed with time. In early to mid-childhood in
girls, as for boys, there was no relation, but beginning at age 11 and continuing until
about age 20, there was a negative correlation between ego control and ego resiliency,
such that for girls during this phase, ego resiliency was correlated with lessening of
overcontrol. After age 20, there was, again, little correlation between ego control and
ego resiliency. These possible developmental differences in factors contributing to ego
resiliency at different ages are intriguing, and they suggest that the relation between
resiliency and appropriately titrated or moderated levels of control may itself be influ-
enced by biological and social forces—some of which we consider in the next section.
to extremely inhibited and rigid behaviors that “appear to be so automatic that they
often are not under voluntary control” (Valiente et al., 2003, p. 1174), whereas
extremely low levels lead to distractibility and impulsiveness.
As developed further in Chapters 8 and 9 (see for example, the last section of
Chapter 9 on “Approach versus Avoidance: Control, Controlling Control, and the
Dynamic Interplay of Cognition and Emotion”), the brain systems contributing to
effortful control and executive functions predominantly involve the frontal-striatal
and anterior attention system (especially the anterior cingulate gyrus and prefrontal
cortex, with projections to the basal ganglia and thalamus; e.g., E. K. Miller & Cohen,
2001; Rothbart & Bates, 1998). By contrast, reactive control is more strongly associ-
ated with frontal-limbic circuits, involving reactive responses to both negative and
positive incentives, such as the amygdala to fear, and the nucleus accumbens to reward
(Martel et al., 2007).
The potential benefits to be derived from possessing a high degree of effortful
control (and the closely related construct of self-control) are readily identified and
well documented. For instance, in seminal work on delay of gratification in children,
involving such simple tasks as not eating a physically present marshmallow or a cookie
so as to earn a second one at a later time, Mischel and colleagues (e.g., Mischel, Shoda,
& Peake, 1988; Shoda, Mischel, & Peake, 1990) found that a greater capacity of young
preschool children to delay immediate gratification was correlated with a wide range
of later cognitive and social competencies during adolescence. Children who showed a
greater capacity for delay of gratification in the preschool test were later reported,
by their parents, to be more socially and academically competent; they were also
characterized as more verbally fluent, rational, attentive, planful, and as having the
capacity to deal well with frustration and stress.
More cogently, preschool delay of gratification performance was related to
objective measures of cognitive control on a demanding task administered more than
10 years later. Individuals who, as preschoolers, successfully intentionally directed
their attention away from temptation (in order to delay gratification, low temptation
focus) showed faster responses to a challenging go/no-go task, without making more
errors, than did peers who were less successful in directing their attention away from
temptation (high temptation focus). Furthermore, the difference between these two
groups was especially prominent in conditions that required higher levels of control
(trials that followed many preceding trials involving a go response). Other benefits of
higher levels of self-control include improved social adjustment and fewer disorders
that centrally involve a failure to curtail or restrain impulses, such as explosive anger,
substance abuse, or criminal behavior (e.g., Caspi, 2000; DeWall et al., 2007).
Many of the benefits of high levels of self-control were succinctly and clearly sum-
marized in the title of a paper by Tangney and colleagues (2004), “High Self-Control
Predicts Good Adjustment, Less Pathology, Better Grades, and Interpersonal Success.”
The paper developed a new questionnaire measure of individual differences in self-
control, designed to broadly assess self-control in relation to controlling one’s
thoughts, emotions, impulses, and performance. Their findings, from two large sam-
ples of undergraduate students, were that, for example, higher scores on the question-
naire correlated with higher grade point average, better relationships, and interpersonal
skills, and less binge eating and alcohol abuse.
196 M O T I VAT I O N A N D E M O T I O N
But is it possible to have too much effortful control? Is more always better, or is
there some point at which very high levels of effortful control become problematic?
This apparently simple but very important question is difficult to answer for
several reasons. One reason centers on definitions of “overcontrol.” Some investiga-
tors argue that what appear to be cases of “too much” control, such as anorexia
nervosa or some obsessive-compulsive disorders, are, instead, cases of misregulated
control. On this view, “the putative category of over-control is simply a misuse of a
desirable capacity rather than an indication that too much self-control is bad” (Tangney
et al., 2004, p. 278). The question also is difficult to answer for the closely related
reason that sometimes what appears to be “too much effortful control” might be over-
control of a reactive sort (that is, not voluntary control but automatically elicited
responses).
Both issues are well illustrated by additional results from the study by Tangney
et al. (2004), relating to other personality correlates of self-control. These investiga-
tors argued that their results yielded no evidence for psychological problems linked to
high self-control. Adding a term to their regression analyses to test for any adverse
effects arising from high levels of control showed no significant increases in predictive
power resulting from the inclusion of a quadratic factor, leading them to conclude that
“self-control is beneficial and adaptive in a linear fashion” (p. 296). Additionally, these
researchers found positive correlations between their measure of self-control and the
“Big Five” measures of conscientiousness and emotional stability, both before and
after controlling for social desirability. (The self-control scale was quite strongly posi-
tively correlated with two measures of social desirability of responding, and all analy-
ses were therefore reported both with and without social desirability as a covariate.)
However, there was a “hint” of a possible form of overcontrol cost related to
a different measure: that of perfectionism. Perfectionism is a mode of responding char-
acterized by the tendency to adhere rigidly to unrealistically high standards and expec-
tations, and it was measured by the Multidimensional Perfectionism Scale (Hewitt &
Flett, 1991, both studies) and a second brief unpublished perfectionism scale (Study 2
only). These measures showed only modest correlations with the self-control measure
(though the “self-oriented perfectionism” subscale of the Multidimensional Scale
showed a significant correlation with the full Self Control scale in both studies, even
after controlling for Marlowe-Crowne Social Desirability). Given these results, Tangney
et al. (2004) proposed that rather than representing a form of overcontrol, perfection-
ism may comprise an example of loss of control—a form of compulsive persistence and
inability to relax that is a form of rigid and nonvoluntary overcontrol (e.g., persistently
working when one should take a break or an inability to relax excessively high standards
when one would like to do so, or it would be adaptive to do so). Whereas rigidly “over-
controlled” individuals (e.g., those with obsessive-compulsive disorder or anorexia)
have difficulties in regulating their capacity for self-control or “lack the ability to con-
trol their self-control,” in contrast, “individuals genuinely high in self-control have the
ability to exert self-control when it is required [. . .] and to suspend self-control when it
is not” (Tangney et al., 2004, p. 314)—as in the notion of the ego-resilient individual.
This in some respects parallels arguments made by Valiente and colleagues (2003)
that, although correlated with one another, overcontrol and effortful control comprise
different constructs. These researchers found that at an initial assessment (Time 1) of
Act ion an d M ot iv at ion 197
Nonetheless, there is some tentative developmental evidence that very high levels
of effortful control may not be adaptive. K. T. Murray and Kochanska (2002) assessed
83 children at each of three ages (normally developing toddlers, an additional
20 children were initially tested but were not available for all three tests): toddler
(approximately 2.5 years), preschool (approximately 4 years), and early school age
(5.5 years). Problem behaviors were assessed with the standardized Child Behavior
Checklist at preschool age. There was a quadratic relation between level of effortful
control and problem behaviors, such that problem behaviors were more frequently
found for children who demonstrated both especially low, and especially high, levels
of effortful control. Follow-up analyses showed that children with higher levels of
effortful control showed more internalizing behaviors than did those children with
moderate levels of control, whereas, compared to this group, children with lower levels
of effortful control showed more attention problems. However, it is possible that the
measure of effortful control also tapped some forms of reactive control (e.g., reactive
inhibition due to punishment; Eisenberg & Morris, 2002).
From a more general perspective, there are also both broader conceptual consider-
ations and specific empirical findings that argue that, as with many good things, too
much effortful control can become problematic (when exercised too relentlessly and
unremittingly). Exceedingly high levels of effortful control may sometimes reduce
flexibly adaptive processing and spontaneity, and also may potentially unduly
constrain an individual’s emotional experiences. There is also considerable empirical
evidence that effortful control may be a “limited resource,” so that at least under some
conditions, effortful exertion that is too continuously prolonged may bring costs to
198 M O T I VAT I O N A N D E M O T I O N
L E V E L S O F C O N T R O L , S P O N TA N E I T Y, A N D O P E N N E S S
TO E X P E R I E N C E
The potential costs of overcontrol—even if never identified as such from a societal
perspective—have been repeatedly emphasized by the initial proponents of the dis-
tinction between ego control and ego resiliency: Jean and Jack Block. These researchers
argue that overcontrol may lead to a “categorical delaying of gratifications or reflexive
rejection of interferences regarding matters both relevant and importunate” (J. Block
& J. H. Block, 2006, p. 318). Stated differently, the habits of control may become overly
generalized and be too readily and peremptorily exercised, so that the highly controlled
individual may sometimes turn away promising opportunities without due consider-
ation or ignore overtures for help or advice that should not be ignored (e.g., because he
or she is highly focused on a given task). Overcontrol might also, in some contexts,
contribute to behavior that is “rigid, unexpressive, routinized, and flattened in affect”
(p. 318). Conversely, although the hazards of undercontrol are real, what might be
considered “insufficient” self-control may also be “the basis for openness to experience,
for flexibility, for expressions of interpersonal warmth, and for creative perceptions or
recognitions” (p. 318). Spontaneity rather than a high level of effortful control may be
important to the expressiveness and receptive savoring of unexpected and unlooked-
for moments of joy that brighten our lives and sustain our hopes and relationships
with one another and with the natural and cultural world. Spontaneity may also be
essential to the open-ended curiosity, exploration, and tolerance of ambiguity that
enable us to expand our behavioral repertoires and knowledge.
Empirical support for this conceptually based proposal that high levels of control
may interfere with spontaneity and emotional expressiveness is provided by an inves-
tigation conducted by Zabelina and colleagues (Zabelina, Robinson, & Anicha, 2007).
This study used the multiple-component self-control scale that had been developed by
Tangney et al. (2004), measuring control of one’s thoughts, emotions, impulses, and
performance, together with several direct and indirect assessments of personality and
emotion. Participants (students) performed modified personality Q-sorts on them-
selves (involving 23 personality terms) as the target, and then also with regard to
themselves in several specific role relations (e.g., describing themselves when they
were with close friends, with strangers, or with their parents). Also, to obtain a more
open-ended assessment of each individual’s characteristic modes of thinking,
participants were asked, for each of seven successive days, to write a passage of
between 300 and 320 words about “What are you thinking?” These passages then were
analyzed using an automated linguistic coding procedure (Pennebaker et al., 2001)
that provides percentage frequencies for particular word categories.
The analyses of the open-ended text passages showed that higher levels of self-
control were significantly negatively correlated with the occurrence of words relating
to emotion or affect (r = –.41); this was equally true for both positive affect (r = –.26)
Act ion an d M ot iv at ion 199
and for negative affect (r = –.32). Likewise, there was a significant negative correlation
between self-control and the occurrence of words that referred to physiological
states (e.g., eat, r = –.30) or to the body (e.g., tired, r = –.35). Thus, higher levels of
self-control appeared to be associated with more abstract modes of thinking, with
fewer connections to emotional and “embodied” aspects of experience. Although not
necessarily detrimental, and sometimes advantageous, such patterns of subjective
experiencing, involving reduced access to specific affective and physiological informa-
tion might also (if too extremely manifested) bear the risks of, for example, decreased
empathy or decreased self-understanding.
A further finding related to the consistency of self-descriptions, as determined
by the Q-sorts, and characterizations of the participants by others who knew
them well. Those higher in self-control showed greater consistency in their behavior
and personality expression across different role contexts, both as assessed by their
own Q-sorts for different roles, and as assessed by the Q-sorts provided by three indi-
viduals who knew them well. These informant ratings also pointed to greater shyness
and less spontaneity in individuals with high self-reported self-control, and to greater
extraversion and spontaneity in individuals with relatively lower self-reported
self-control.
These outcomes comprise what Zabelina and colleagues (2007) refer to as potential
“psychological tradeoffs” of self-control, and they offer some support for the long-held
position of the Blocks outlined earlier. From another (albeit related) viewpoint, these
findings are also broadly consistent with conclusions reached by Zimbardo and
colleagues, based on a series of studies evaluating individual differences in perspec-
tives on “psychological time.” Zimbardo and Boyd (1999) contrast individuals who are
highly and consistently oriented toward the future (strongly emphasizing future goals
and plans, resistance to temptation, and thus both high self-control and likely also a
high level of abstraction) versus individuals who have one of several other predomi-
nant orientations toward time. Other time perspectives differentiated by these
researchers include “past-negative,” characterized by a largely aversive orientation to
the past; “present-hedonistic,” featuring high levels of impulsiveness and orientation
to present pleasures with little concern for future consequences, and correlated with
both ego undercontrol and sensation seeking; “past-positive,” characterized by a
warm, sentimental attitude toward the past; and “present-fatalistic,” entailing a fatal-
istic, helpless, and hopeless attitude toward the future and life.
A too-extreme immersion in any one of these time perspectives has undeniable
drawbacks, yet the clear and many benefits that can be gained from a future time
perspective may lead individuals to adopt it too continuously and too uniformly. Thus,
Zimbardo and Boyd (1999, p. 1285) express concern for “those excessively future-
oriented people who cannot ‘waste’ time relating to family or friends, in community
activities, or enjoying any personal indulgence” and who, though successful in their
careers, are unsuccessful in life, because they lack “a broader temporal perspective in
which to integrate work, play, and social responsibility.” These investigators specifi-
cally argue that an adaptively changing “balanced time perspective” is the most healthy
both psychologically and physically, and optimal for societal function:
In line with these arguments that an ever-faithful and ever-strong adherence to the
demands of the far future may not always be beneficial is evidence that individuals
may come to regret their past choices of high levels of self-control. In contrast to the
“myopia” that has been the predominant focus of concern in the classical literature on
self-control, there is evidence that people “sometimes suffer from excessive farsight-
edness and future-biased preferences, consistently delaying pleasure and overweight-
ing necessity and virtue in local decisions”—a form of excessive restraint termed
“hyperopia” (Kivetz & Keinan, 2006). For instance, students in their second year of
university who were asked to evaluate any regrets that they had about how they had
spent their winter break not infrequently endorsed regrets at having too much
self-control. The degree to which they endorsed such regrets (e.g., “I should have
enjoyed myself more,” “I should have traveled more”) was greater for their winter
break 1 year ago than 1 week ago. Although for the winter break that had just passed,
participants more strongly endorsed regrets about not studying and not working more
often (so-called virtue regrets) than about not enjoying themselves and not traveling
(“indulgence regrets”), these patterns reversed when they reflected on the winter
break of the year before.
Taking part in such activities as leisure travel is sometimes construed in negatively
value-laden terms (e.g., as being wasteful or irresponsible). Yet unduly weighting this
viewpoint may lead some people to repeatedly forfeit precisely those activities that
they enjoy the most, and also to forgo important new opportunities for learning and
exploration.6 Thus although many of us clearly do experience significant problems
deriving from a too-ready acquiescence to “indulge” (very broadly construed), others
may experience a too-ready and too-persistent “weakness for necessity.” In the long
term, the latter individuals may more often and more completely abstain from pur-
suits that they really wish they would undertake, even though, at the time, the strong
voice of necessity would always trump those pursuits. People in the latter category
may sometimes adopt deliberate strategies aimed to overcome their “weakness for
necessity”—for instance, by precommitting to indulgence in the form of prebooked
holidays or choosing specific “luxury prizes” over their cash equivalents (Kivetz &
Simonson, 2002). Individuals may also opt for this approach on behalf of friends and
loved ones, choosing a particular product or outcome over more fungible cash rewards
precisely so as to “force” their loved ones to “indulge” rather than to save or spend on
necessities.
In summary, there are both positive and negative implications that arise from too
uniformly and consistently high levels of control; equally, both positive and negative
implications arise from relatively lower levels of control. Within a fairly broad range of
possible degrees of control, it might be argued that the level of control one exerts is,
on its own, “neutral” and that the adaptive value of a given degree of control is
determined by contextual and individually modulated factors. Ego resilience is an
important construct in relation to agile thinking because it directly and explicitly
recognizes the need for variable and modulated control, and the complex relations
of levels of control to exploration, positive affect, and the development of new
Act ion an d M ot iv at ion 201
“ S E L F - R E G U L ATO R Y D E P L E T I O N ” — I S E F F O R T F U L
SELF-CONTROL A LIMITED RESOURCE?
Another important reason to question whether exercising more effortful self-control
is invariably beneficial derives from arguments and evidence that the capacity for
effortful self-control is a limited resource—not only in the sense that we have limited
attentional or central executive and working memory capacity at any one moment in
time, but that we have limited executive control resources over time. It has been
argued that expenditure of this resource, through acts requiring effortful self-regula-
tory control, will lead to fewer available resources if a further situation requiring self
control is encountered, before this capacity has had an opportunity to be “replen-
ished.” This is a central claim of the “ego depletion” or “self-regulatory depletion”
account of self-regulation and of failures in self-regulatory behavior that has been pro-
posed by Baumeister and colleagues (e.g., Baumeister, 2003; Baumeister, Bratslavsky,
Muraven, & Tice, 1998; Baumeister, Muraven, & Tice, 2000; Vohs & Heatherton,
2000; for recent meta-analysis, see Hagger et al., 2010. See also the “Attention
Restoration Theory” proposed by S. Kaplan, 1995, 2001, that similarly emphasizes the
fragility and vulnerability to fatigue of voluntary “directed attention” and that, as
developed in Chapter 11, provides a conceptual analysis and evidence regarding the
types of experiences that are likely to lead to recovery from such fatigue).
Stated simply, Baumeister and colleagues suggest that, “controlling oneself—
especially when this involves overriding one’s own impulses, habits, or established
tendencies—consumes some limited resource.” Further, they suggest that, “This
resource resembles an energy or strength. When it is depleted, people become less
able to control themselves” (Baumeister et al., 2000, p. 131). To the extent that this is
true (and we will consider and evaluate some of the evidence for this view later)
it might also suggest that individuals characterized by a moderate modal level of
control will be more resilient and adaptively flexible because more often they
will move between periods of highly effortful control and less controlled/more
automatic/more spontaneous processing modes, during which control resources may
be “replenished.”
According to Baumeister and colleagues, diverse sorts of self-control activities
depend upon the same (single form) resource, such that one and the same resource is
called upon if the individual is attempting to regulate his or her emotions, to control
impulses, to suppress thoughts, to initiate actions, to deliberately enhance perfor-
mance, or to make responsible choices or decisions. The posited scarcity of the self-
regulatory resource is based, in part, on evidence that self-control failures occur quite
frequently and are more likely at particular times (e.g., late rather than early in the
day, and when under stress), suggesting, at least on the face of it, that ego depletion
202 M O T I VAT I O N A N D E M O T I O N
itself may be a quite common occurrence (e.g., Baumeister, Vohs, & Tice, 2007;
Vohs & Faber, 2007; Vohs & Heatherton, 2000). Notably, self-regulatory depletion is
proposed to occur specifically after engaging in activities that demand any of several
forms of self-control, not simply the concentrated expenditure of energy in a more
generic manner. For example, whereas avoiding thinking of a forbidden topic
(intentional thought suppression) led to reduced self-regulatory capacity on a subse-
quent task, solving difficult multiplication problems did not (e.g., Muraven et al.,
1998). It is further argued that:
were not asked to refrain from eating any of them (Baumeister et al., 1998,
Experiment 1).
(iv) Attention control: Undergraduate participants who were asked to perform a
demanding letter cancellation task (involving multiple rules for the letter
cancellations and difficult-to-read text) and who were then requested to watch
a tedious video in order to be able to correctly answer questions concerning it,
showed greater passive than active choosing than did participants who had
performed an easy letter cancellation task. Those in the demanding letter
cancellation condition watched more of the movie when the method that they
needed to use in order to indicate that they wanted to discontinue watching
required that they make an active response (pressing a signal button) than
when they could indicate that they wanted to discontinue watching the film by
making only a passive response (releasing the signal button from a “default”
pressed position). In contrast, those who had earlier performed the easy letter
cancellation task were equally likely to indicate that they wanted to stop
watching the movie by actively pressing or passively releasing the signal
button.
(v) Thought suppression: Under the guise of a marketing study for the university
bookstore, undergraduate participants who had earlier been asked to suppress
thoughts concerning a particular topic when later offered the opportunity to
spend money on various products chose to spend significantly more money
than did individuals not asked to suppress (actual dollars spent). This effect
was especially pronounced for persons with a stronger general predisposition
to impulsive spending (Vohs & Faber, 2007, Experiment 2), and it was
observed both for the purchase of products that would be considered healthy
and for purchases of products likely deemed unhealthy (Experiment 3).
The latter outcomes, in which persons who had engaged in an earlier task that
demanded effortful self-regulation then spent more of their own money on available
products than did individuals in the control condition, suggest that the potential
effects of self-regulatory depletion may not be confined to behavioral indices of par-
ticipation in what might be construed as essentially “inconsequential” laboratory
tasks, and also are not confined to tasks that may be impossible to solve (as in cases ii
and iii described earlier). Several further studies have strongly supported the potential
“real world”7 and more complex cognitive effects of self-regulatory depletion, includ-
ing on measures that directly involve flexible, on-the-spot thinking and judgment.
For instance, using initial depletion tasks that required individuals to either actively
regulate their attention or to suppress emotion, Schmeichel, Vohs, and Baumeister
(2003) found that individuals who had performed these demanding self-regulatory
tasks showed impaired performance on several complex judgment and reasoning
tasks. The tasks included measures of logic and reasoning (Graduate Record
Examination tests of analytical reasoning), a measure of complex reading comprehen-
sion (GRE reading comprehension), and a measure of fluid intellectual reasoning
(the Cognitive Estimates Test, requiring the flexible on-the-spot use of prior knowl-
edge to answer questions for which the answers are not known, but that can be
approximated using reasoning and related knowledge, such as “How many seeds are
204 M O T I VAT I O N A N D E M O T I O N
to subsequent tasks that may continue to exert demands on such control, precisely
how best to construe the “self” in “self-regulatory control” remains unclear. It has
been proposed that self-regulatory control and associated decreases in glucose might
lead to increased reliance on heuristic-based “System 1” cognitive processes at the cost
of effortful “System 2” reasoning (e.g., Masicampo & Baumeister, 2008; see Chapter 1
discussion of dual-process accounts of cognition). However, recent findings pointing
to apparently similar depletion effects in domesticated dogs suggest that care must be
taken not to “overfit” an account to humans and human cognition. H. C. Miller and
colleagues (2010) found that dogs demonstrated both decreases in “self-control” (per-
sistence at an unsolvable task) as a consequence of earlier self-control exertion and
increased persistence after being provided with a glucose drink (compared with a sug-
ar-free control drink). Specifically, dogs that were required to sit and stay in
solitude for 10 minutes showed less persistence in attempting to obtain food from a
“puzzle-toy” than did dogs left in their cages for a corresponding amount of time;
furthermore, providing the dogs with a glucose drink eliminated the detrimental
effects of the earlier demanding “sit-and-stay” control task on the animal’s
persistence. As suggested by H. C. Miller and colleagues (2010, p. 537), “The ability to
coordinate rule-based memories and current behavior in a goal-directed way is perva-
sive across species.” The parallel findings in humans and dogs argue that there
are potentially important biological commonalities between human and nonhuman
“self-control” or “executive-control” processes. These simultaneously suggest that we
should take care not to tailor self-regulatory accounts to human cognition too
narrowly, and they provide exciting new research avenues for exploring basic similari-
ties and articulation of differences in executive-control processes across species.
Beyond the psychobiological intervention of increasing available glucose, many
further cognitive and motivational factors may modulate the occurrence of self-
regulatory depletion in humans. One key factor is how one thinks of the action of
self-regulation, and also one’s manner of responding. Changing the construal of a
given task, and how and to what one allocates one’s attention, may change the degree
of difficulty it poses. For instance, preschool children who thought of marshmallows
as “clouds” or pictures showed greater resistance to temptation and longer delay of
gratification than did children who focused on the soft texture and taste of the
marshmallows (e.g., Mischel & Moore, 1980; B. Moore, Mischel, & Zeiss, 1976).
Implicit assumptions and priming effects may also moderate how individuals
respond to self-regulatory challenges. Questionnaire data (Martijn et al., 2002,
Experiment 2) indicate that individuals explicitly endorse a view of self-control as
energy (e.g., “After completing an exacting task, I take some time to relax,” “Controlling
intense emotions wears me out”). However, the alternative view—that self-control
involves a “state of mind,” such that if you want to and try hard you can always control
yourself—was also endorsed, though somewhat less strongly (e.g., “I perform better
when I am under pressure,” “Sometimes when I feel that I am finished, I can do a lot
more than I thought”).
Martijn et al. (2002) found that presenting information that challenged assump-
tions about the general resource and use of “energy” for self-control tasks significantly
changed the patterns of outcomes that were observed. Participants first watched a
highly aversive video (that evoked disgust) either with instructions to suppress their
208 M O T I VAT I O N A N D E M O T I O N
Consistent with this proposal, participants who were implicitly primed with the
ideas of persistence and perseverance in a scrambled sentence task showed no
decrement in hand-grip duration following a challenging labyrinths task, whereas
participants in a neutral priming condition who performed this difficult task showed
the typical self-regulation-related decrement (Alberts et al., 2007). This pattern was
Act ion an d M ot iv at ion 209
replicated in a further study using difficult versus easy calculations as the initial task,
and a different implicit prime manipulation. In a meta-analysis of the moderation of
the self-regulatory depletion effect by motivational strategies, Hagger et al. (2010)
found a large effect size; additionally, congruent with a conception according to which
self-regulation is likely influenced by multiple psychological and contextual factors,
there was also significant heterogeneity of effect sizes across studies.
Further evidence suggests that the inducement of mild positive affect also may
attenuate or eliminate the effects of self-regulatory depletion. Following an initial act
of self-regulation, individuals who were given a small surprise gift or who watched a
comedy film subsequently performed as well as did control participants, who had not
been challenged to self-regulate, on new tasks that required effortful self-regulatory
control—and outperformed individuals who instead were exposed to an emotionally
neutral or sad stimulus, or were given a brief rest break (Tice, Baumeister, Shmueli, &
Muraven, 2007).
Thus, a construal of self-control as a matter of a limited and fixed amount of energy
alone is far too simple: Self-regulatory behavior also is strongly modulated by both
conscious and implicit expectancies. In addition, as noted earlier, and shown by the
results of Webb and Sheeran (2003), we can use implementation intentions (a form of
“strategic automatization”) to proactively reduce demands on self-regulatory control.
Individuals who formed implementation intentions relating to when and how to act
during a depletion task later performed better on a self-regulatory task than did indi-
viduals who did not form such intentions—suggesting that automatic processes could
be proactively brought to bear to conserve effortful controlled processing resources.
An overly simplified construal of self-control as a highly limited and fixed quantity
resource also fails to accommodate evidence that forms of executive capacity such as
working memory and attention control may be enhanced through training or regular
practice. In one prominent example, healthy adults who engaged in several weeks of
training on three visual-spatial working memory tasks in which the difficulty level was
systematically incremented across sessions showed continuous improvements on
each of the three tasks (Olesen, Westerberg, & Klingberg, 2004). Similarly, 3- and
4-year-old children repeatedly given tasks that required inhibitory control and the
flexible modulation of their behavior in response to changing rules, together with
explicit feedback on their performance, later showed improved response control
and executive functions on a different go/no-go discrimination learning task than did
children simply given intervening practice (with no explicit feedback) on the go/no-go
task (Dowsett & Livesey, 2000; also see Kramer, Larish, & Strayer, 1995). These and
other important intervention procedures shown to enhance the capacity for forms of
flexible thinking that require executive control are discussed further in Chapter 11.
Here, however, it is noteworthy that there is also some evidence that individuals
can increase self-regulatory strength through regularly engaging in tasks that require
effortful control (Gailliot, Plant, Butz, & Baumeister, 2007; see also Muraven, 2010;
Oaten & Cheng, 2007). In a series of studies, healthy young adult participants were
asked, over a period of 2 weeks, to either write with their nondominant hand or to
change how they normally spoke, for example, avoiding slang, swear words, and col-
loquialisms for the words “yes” or “no,” and speaking in full sentences (self-regulatory
training manipulation). They then took part in a “stereotype suppression task” in
210 M O T I VAT I O N A N D E M O T I O N
which they were asked to either describe a particular type of person without making
any references to stereotypes or to take part in a brief social interaction with a person
who was a member of the often-stereotyped category. This was the self-regulatory
control challenge. Participants were also preexperimentally tested for internal and
external motivation to avoid using stereotypes. Specifically, participants were selected
to be either low in both forms of motivation (and so were likely relatively unpracticed
at engaging in stereotype suppression) or high in either internal or external motiva-
tion (and so were likely comparatively more practiced at engaging in stereotype sup-
pression). The self-regulatory control challenge was both preceded by and followed by
(across the different studies) a further assessment of self-regulatory performance,
including either a difficult anagram task or a Stroop color-word interference task.
It was predicted that, relative to the individual’s original anagram or Stroop perfor-
mance, the stereotype suppression task would lead to a decrease in self-regulatory
control on the second anagram or Stroop interference task, but only for individuals
who were low in motivation to avoid stereotyping, and so comparatively unpracticed
at doing so (thus requiring more effortful control during the stereotype suppression
phase). It was further predicted that the longitudinal self-regulatory training manipu-
lation would attenuate or eliminate the adverse effects of the stereotype suppression
task on the subsequent anagram or Stroop interference tasks, but particularly so in
the low motivation group—because only they were expected to show decrements in
self-regulatory control as a function of the relatively unfamiliar and thus effortful
requirement to suppress the use of stereotypes.
The results were in line with both of these predictions. In each of three longitudinal
experiments, the regular exercise of self-regulatory control over the preceding 2 weeks
acted to alleviate the behavioral costs that were associated with the effortful suppres-
sion of stereotypes, with this benefit largely confined to those participants who were
assumed to have had the least prior practice at inhibiting stereotypes because they
reported low motivation to do so. Beneficial effects of prior training in self-regulatory
control, with training leading to improved performance on self-control tasks and
attenuated self-regulatory depletion, also were found in Hagger et al.’s (2010) meta-
analysis of self-regulatory training studies; again, however, the significant positive
effect size was accompanied by considerable heterogeneity of effect sizes across the
nine tests that were included. This effect size heterogeneity suggests that, like self-
regulatory depletion, the success of efforts to increase self-regulatory control through
systematic exercise or “training” is likely modulated by a number of factors.
Three final points relating to self-regulatory control, and its relation to the iCASA
framework, need to be emphasized. First, Baumeister et al.’s (1998) characterization
of what the “resource” is that is depleted by the exercise of volition/control explicitly
links self-regulatory control to levels of representation, particularly the capacity for
accessing and acting upon more abstract goals even under conditions that render this
more difficult. They suggest that it is a “resource that functions to connect abstract
principles, standards, and intentions to overt behavior” (Baumeister, Bratslavsky,
Muraven, & Tice, 1998, p. 1263; also cf. Magen & Gross, 2007). The further statement
that “Even a small amount of this resource would be extremely adaptive in enabling
human behavior to become flexible, varied, and able to transcend the pattern of simply
responding to immediate stimuli” (p. 1263) again links control to the capacity for
Act ion an d M ot iv at ion 211
The fundamental concept that alternating between time periods involving highly
controlled and highly complex forms of thinking versus periods involving relatively
familiar, mildly emotionally positive, and predominantly automatically completed
activities has also recently been explicitly forwarded as a strategy for fostering
creativity in the workplace, particularly among “chronically overworked profession-
als.” Elsbach and Hargadon (2006) proposed that interspersing phases of what they
termed “mindless” work (that is, work that is low in both cognitive difficulty and pres-
sures relating to performance) with phases of much more cognitively challenging and
high-pressure work should lead to enhanced creative productivity. Although such
work might be better described by their alternative expressions of “recharge time” or
perhaps (depending on the context) “hands-on time,” their proposal (further discussed
in Chapter 12, together with recent related empirical findings) coheres well with the
evidence reviewed in this section.
All of these possibilities clearly merit further research and conceptual clarification.
Research incorporating a consideration of individual differences in how we respond to
situations that may be resource depleting (or replenishing) is also essential. For
instance, Shamosh and Gray (2007) found that individuals who scored high on a
measure of fluid intelligence (Raven’s Advanced Progressive Matrices) were more
susceptible to resource depletion than were individuals who scored lower on this mea-
sure, even though this difference was not associated with differences in performance
on the resource-demanding task that they used (an emotion suppression task). Stated
differently, it appeared that the high fluid intelligence participants experienced a
greater cost to regulatory resources, with no corresponding increment in performance.
Although this finding is consistent with evidence linking fluid intelligence with
executive control and working memory functions, it raises important questions about
longer term patterns of resource depletion versus replenishment that might help to
offset greater costs. Indeed, Shamosh and Gray (2007, p. 1841) suggest that it is
plausible that “long-term optimization of resource allocation profits from a greater
initial investment of resources during relatively novel self-regulatory challenges.”
Third, and finally, many of the experimental tests of self-regulatory depletion
have involved an externally determined, and in some respects essentially arbitrary,
imposition of demanding tasks on individuals (e.g., watching an emotional film while
suppressing emotional expressions of responses to the film; here the participants have
no strong internally driven reason for such suppression, as might arise if one is
suppressing emotional responses in order to avoid distressing a child or a loved one).
Yet many of the highly demanding self-regulatory activities that we regularly engage
in are self-determined rather than directly determined by others. This raises the
important question of whether the degree to which self-regulatory depletion arises
from performing a given self-regulatory task, or making particular decisions, also is
moderated by whether the task or decisions are self-determined.
According to a theory of self-determination proposed by Deci and Ryan (e.g., 1987),
the forms of regulation that we undertake differ, depending on what we perceive as
the origins of the regulation and the degree of autonomy and volition versus control
and pressure that we exercise in so acting. As used by these theorists, autonomous
regulation refers to regulation that is “initiated and sustained by one’s integrated, or
true, self.” In contrast, controlled regulation “encompasses regulation by aspects of
Act ion an d M ot iv at ion 213
the person that are less well integrated with the self.” More specifically, “controlled
regulation involves feeling pressured, coerced, or seduced into action, whereas auton-
omous regulation involves doing what one finds interesting or important and would
be inclined to do more freely” (Moller, Deci, & Ryan, 2006, p. 1025).
To examine the effects of controlled versus autonomous choices on regulatory
depletion, Moller and colleagues (2006) modified a paradigm used by Baumeister et al.
(1998). In that paradigm, undergraduate participants allegedly taking part in a study
on responses to persuasion who had chosen to give a speech that either agreed
with their own attitudes or disagreed with their attitudes toward a tuition increase
(but had not actually made the speech) subsequently showed reduced persistence on a
difficult (impossible) figure-tracing task compared with individuals who were not
asked to make a choice about giving a speech. Decreased persistence was shown both
by less time spent on the figure-tracing task and a decreased number of attempts to
solve it (Baumeister et al., 1998, Experiment 2). Baumeister and colleagues inter-
preted these outcomes as suggesting that not only resisting temptation but also
making responsible choices may decrease the availability of “self-control” resources.
However, Moller et al. (2006) observed that, in the earlier study, what appeared to be
a free choice by the participant actually comprised a controlled choice in that the exper-
imenter strongly encouraged the participant to opt for making the speech with regard
to one rather than another position. Participants were given the cover story that
because there were already enough participants who had chosen one of the speech
topics, it would help the study a great deal if they chose the other topic. In fact, all
participants then chose the topic that the experimenter said would substantially help
the study, suggesting that participants may have felt pressured to comply with the
experimenter’s request.
Moller and colleagues (2006) modified the paradigm so that three choice condi-
tions were included: no choice, controlled choice (with a cover story very similar to
that used by Baumeister et al., 1998), and free choice (no constraints on the speech
topic to be given). Comparisons of these conditions showed that persistence on the
figure-tracing task (both number of attempts and time on task) was significantly
greater in the free choice condition than in the controlled choice condition (Moller
et al., 2006). A similar outcome was obtained in two further experiments using
different choice tasks and also different tasks on which to measure subsequent persis-
tence. Additional manipulation checks confirmed, as expected, that participants did
experience their choices as more self-determined in the free choice than in the forced
choice conditions. Furthermore, a mediation analysis following the guidelines devel-
oped by Baron and Kenny (1986) demonstrated that perceived self-determination
mediated the persistence effect. In contrast, the differences in persistence did not
appear to be related to participants’ evaluations of how interesting or intrinsically
rewarding they found the tasks to be.
Thus, not all sorts of choices place similar demands on us, or equally consume self-
regulatory resources. Additional research has further established the important
contribution of an individual’s level of experienced autonomy in mediating the extent
to which particular tasks prove to be depleting of self-regulatory resources (see
Muraven, Gagné, & Rosman, 2008), suggesting that it is not only what the task
requirements are but also the reasons behind an activity, and the broader context in
214 M O T I VAT I O N A N D E M O T I O N
which a given activity is pursued, that determine the degree to which it draws
upon self-regulatory capacity. It is to these questions of the varying degrees of self-
determination that we may experience in embarking on, and persisting with, a given
course of action that we now turn.
Forms of Motivation
I N T R I N S I C A N D E X T R I N S I C M OT I VAT I O N A R E O F T E N
C O N J O I N E D — R AT H E R T H A N O P P O S E D — A I D S TO
AGILE THINKING
When we say of someone that he or she is “intrinsically motivated,” we are describing
several interrelated aspects of how and why the person approaches an activity or
pursuit. We are noting that the person engages in the activity predominantly for its
own inherent interest, for the joy and love of the activity, including the process of
discovery and creation itself, rather than for the sake of the “extrinsic” rewards,
incentives, or disincentives associated with it. Thus, intrinsic motivation involves
elements such as curiosity, enjoyment, and interest as well as aspects of self-
determination, task absorption, and a healthy relishing of the various sorts of
challenges and opportunities for mastery that a given pursuit offers. In contrast, the
elements most associated with extrinsic motivation involve a focus on financial or
other tangible incentives related to a pursuit, and concerns with competition, evalua-
tion or recognition by others, as well as “other-imposed” (rather than self-determined)
constraints (Amabile et al., 1994).
The central relevance of this distinction to flexibly adaptive thinking lies in the
assumption that intrinsic motivation itself is conducive to such modes of thinking.
As succinctly summarized by Shalley, Zhou, and Oldham (2004), “Scholars have long
argued that individuals are likely to be most creative when they experience high levels
of intrinsic motivation [. . .] since such motivation increases their tendency to be
curious, cognitively flexible, risk taking, and persistent in the face of barriers [. . .] all
of which should facilitate the development of creative ideas” (p. 935).
Research has largely supported this viewpoint (e.g., Hirt, Levine, McDonald, &
Melton, 1997; Koestner, Ryan, Bernieri, & Holt, 1984; Kruglanski, Friedman, & Zeevi,
1971). However, there is a second and different claim that, although also supported to
some extent (e.g., Amabile, 1985), receives much more qualified and limited support.
This second claim, which merits close critical examination, is that there is a negative
or “adversarial” relation between intrinsic and extrinsic motivation. In particular, it
has been found that providing individuals with extrinsic rewards for performing an
activity that they already “intrinsically enjoy” and would pursue in the absence of the
rewards undermines or diminishes the intrinsic motivation they experience (see Deci,
Koestner, & Ryan, 1999, for review). Thus, once the reward is removed or no longer
forthcoming, these individuals are less motivated to engage in the activity than they
would have been had no extrinsic rewards earlier been forthcoming. Extrinsic rewards
also may have other effects, such as decreasing the amount of incidental learning that
individuals show—that is, learning that occurs without a specific motive or formal
Act ion an d M ot iv at ion 215
B E Y O N D A B I P O L A R C O N T R A S T, A N D D I F F E R E N T I AT I O N S
W I T H I N E X T R I N S I C M OT I VAT I O N
The differentiation between intrinsic and extrinsic motivation does not necessarily
imply that these reside on a single underlying dimension. Extensive data collected
from several adult samples (Amabile et al., 1994) have shown that the two forms of
motivation are largely independent of one another, and so may be best conceived as
two unipolar constructs rather than a single bipolar one. Thus, an individual may be
high on one form of motivation (e.g., intrinsic) and low on the other (extrinsic),
but each of the other combinations are equally possible: individuals may be high
on extrinsic but low on intrinsic motivation, low on both intrinsic and extrinsic
motivation, or high on both.
In a large-scale investigation with data collected over a period of several years and
from several samples of college students and working adults, Amabile et al. (1994)
reported a correlation of –.08 between the Intrinsic and Extrinsic Motivation scales of
their Work Preference Inventory for adults (total sample of 1,055 individuals) and a
correlation of –.21 for students (total sample of 1,363 undergraduates). Using
the Academic Motivation Scale (Vallerand & Bissonnette, 1992) with a sample of
171 university students, Walker et al. (2006) reported essentially no correlation
between the intrinsic and extrinsic measures (Pearson r = .02). Analyses of the number
of individuals who scored high on both scales likewise pointed to the relative indepen-
dence of the Intrinsic and Extrinsic Motivation scales. Similarly, Amabile et al. (1994)
216 M O T I VAT I O N A N D E M O T I O N
R E WA R D I N G C R E AT I V I T Y
The evidence that extrinsic rewards may decrease creativity is mixed and not entirely
clear. One contributor to the lack of clarity derives from the fact that the procedures
and instructions adopted did not always clearly indicate to the participants that
creativity—rather than various other possible dimensions of performance, such as
organization or efficiency or conventionality—was desirable, or to be rewarded
(e.g., Eisenberger & Rhoades, 2001). If the conditions that need to be met to receive
rewards are left vague or underspecified, then individuals may default to assuming
that what is to be rewarded is conventional or standard behaviors. (The final section of
this chapter will consider evidence for the marked effectiveness of explicit contingen-
cies that reinforce the generation of novel rather than repeated behaviors.)
Eisenberger and Selbst (1994) showed that rewarding fifth- and sixth-grade
children for divergent thought on one task (constructing six new words from the
letters of given words, such as “instrument” or “brontosaurus”) was associated with
increased originality on a subsequent task (picture drawing incorporating predrawn
circles, such that the circle was a main part of the picture). In contrast, rewarding low
levels of divergent thinking (asking for only one new word to be generated) decreased
originality on the second task. Two independent raters assessed originality, with
Act ion an d M ot iv at ion 219
pictorial subjects that were rarely produced by the children assigned higher originality
scores. However, these results were found only for a small reward; when a large reward
was used, this outcome was not found. Under these large reward conditions, individu-
als in both the high and low divergent training conditions looked similar to the
no-reward condition.
In a further series of experiments (Eisenberger & Armeli, 1997), fifth- and
sixth-grade children were first asked to provide, and were rewarded for providing,
either usual or novel uses of common objects. Those children given a large reward for
producing novel (rather than usual) uses of objects generated pictures that were
judged to be more original (rarer among the topics produced overall) than did children
in any of the remaining conditions (no reward/usual uses, no reward/novel uses, or
small reward for either task). They also more often chose to try to produce novel
drawings rather than to copy a familiar drawing than did children who received
a large reward for generating usual uses.
Although the reasons for differential effects of small versus large rewards on
creative behavior remain unclear, the findings do not support the view that rewarding
divergent or creative thinking necessarily undermines such activities—and provide
some (albeit not complete) support for the view that reward may increase originality
or divergence of thought. Additional studies (Eisenberger & Rhoades, 2001) using
different dependent measures (e.g., the creativity of titles offered for a movie or a
story) and populations (e.g., undergraduates, organizational employees) were similarly
consistent with this conclusion, though other factors, such as precisely how the poten-
tial for reward is construed or “framed,” may also be important (Friedman, 2009).
In an attempt to evaluate creativity in relation to the expectancy of reward in more
everyday contexts, Eisenberger and Rhoades (2001) assessed the creativity of ideas
that employees generated in response to a questionnaire that asked for suggestions
concerning how the organization might either reduce costs or increase profits (Study
5), and also supervisor’s evaluations of the creativity level of the employees (Study 4).
Measures were also included to assess the degree to which employees perceived a rela-
tion between job performance and reward (e.g., “Good performance in my job leads to
higher pay”) and either employees’ self-reported intrinsic task interest in their work
(e.g., “My job is interesting,” “My job is enjoyable,” Study 4) or their perceived self-
determination at work (e.g., “I have the freedom to adopt my own approach to the job,”
“My job allows me opportunity for independent thought and action”). In both studies,
structural equation models showed a significant positive relation (standardized path
coefficient) between the measures of performance-reward expectancy and intrinsic
interest/perceived self-determination; there was also a significant positive relation
between intrinsic interest/perceived self-determination and creativity, but no signifi-
cant direct relation between performance-reward expectancy and creativity. Thus,
performance-reward expectancy exerted effects on the aspects of intrinsic interest or
perceived self-determination, and these, in turn, were related to the two different
measures of creativity.
The following section further examines the effects of reward on behavior, focusing
particularly on behavioral variability. Here, however, a final point might be made
concerning an important implication of the construal of intrinsic and extrinsic
motivation as two unipolar constructs—rather than a single bipolar one. Given that
220 M O T I VAT I O N A N D E M O T I O N
that were produced. These examples will then be followed by demonstrations of how
training in variability may have important adaptive consequences for thinking and
problem solving beyond the trained-on behavior itself. Thereafter, broader theoretical
considerations relating to the origins of variability and connections to other principles
of behavioral modification, including important caveats on the conditions under
which variability is likely to be elicited, will be outlined. Finally, we will consider
the role of variability in individuals’ strategic approaches to problem solving and
important proposals that such variability may both reflect, and build upon, aspects of
both highly practiced, often repeated, and familiar procedures that may be automatic,
and more controlled meta-cognitive evaluations, revisions, and extensions of current
and ongoing problem-solving efforts.
T R A I N I N G I N VA R I A B I L I T Y : E M P I R I C A L D E M O N S T R AT I O N S
An early study of the “training of variability” involved the block building of preschool
children (Goetz & Baer, 1973). The participants were three 4-year-old girls from
a university preschool classroom, selected because, based on the informal reports of
classroom staff, they showed little sophistication in block building, tending either to
simply lay the blocks out in different flat shapes (without construction) or to repeat
the same few simple constructed forms on each occasion (e.g., the same “castle”).
Goetz and Baer (1973) first included several baseline sessions to assess the types of
block constructions the children made and also derived a list of some 20 different
basic types or forms of block constructions that were commonly observed in other
children’s block constructions (e.g., ramp, tower, arch, storied arch, and balance).
Using an “ABA” experimental design, in which they first reinforced one behavior
(Phase A), then reinforced another behavior (Phase B), and then returned to reinforc-
ing the initial behavior (the second Phase A), the researchers systematically altered
the contingencies of social reinforcement (a teacher’s responses to the block construc-
tions that the child produced). Each phase was comprised of several individual one-on-
one block-building sessions during which the child was either consistently reinforced
for making forms that were different from ones she had made previously during the
session (e.g., “Oh, that’s very nice—that’s different!”), or for repeating forms she had
already made within the same session (e.g., “How nice, another arch!”). Each child was
first reinforced (in several sessions) for varied and novel responses (Phase A), then
reinforced for repetitions of same responses (Phase B), and then once again reinforced
for varied and novel responses (return to Phase A).
All three children showed a clear and steady increase in the diversity of forms
created during the phases in which only different forms were followed by reinforce-
ment. This pattern of increasing form diversity was reversed and began to decline in
Phase B when reinforcement was, instead, given only for repeated forms, but again
increased when reinforcement for different forms was reintroduced. By the end of
training, all three children also showed markedly higher diversity in their block
constructions. Whereas during the baseline sessions, each child produced only between
one and four different forms, by the end of the training, the children were producing
between 11 and 18 different forms—even though, at no point, were the children
provided instructions as to how to make different block forms.
222 M O T I VAT I O N A N D E M O T I O N
In this study, the criterion for “not repeating” was relative, in that reinforcement
was provided for block constructions that had not previously been produced within
the given experimental session, rather than ones that were necessarily unique (though
the different “forms” were themselves actually classes or types, and so, at a more
specific level, some of the children’s constructions may have been unique). A relative
criterion may be more pragmatically tractable than a criterion that requires “absolute”
novelty. It is very difficult (sometimes impossible) to accurately assess absolute
novelty (an evaluation that requires knowledge of the entire history of the individual),
particularly when such assessment needs to occur very rapidly, so that reinforcement
of the novel behavior can be either given immediately, or be withheld, as appropriate.
Our second example, from a rather different domain, used a criterion closer to the
latter sort. The initial motivation for the study by Pryor, Haag, and O’Reilly (1969)
was simple, if unusual: One of the authors was working at Sea Life Park in Oahu,
Hawaii, and introduced into the five public daily performances at the Ocean Science
Theater, a demonstration of reinforcement of previously unconditioned behavior.
The subject was a female rough-toothed porpoise, named Malia. Here—because
the demonstration was designed to show the effects of reinforcement on previously
unconditioned behavior—the criterion for reinforcement was (as far as possible)
absolute novelty. As the authors describe, in the face of this requirement to find a new
behavior that would be reinforced in each of five brief daily sessions, the behavior of
Malia changed remarkably:
responses, she had never been reinforced for showing “spontaneous activity.” Indeed,
other Sea Life trainers characterized her as “a docile, timid individual with little
initiative” (Pryor et al., 1969, p. 654). Nonetheless, as in the case of Malia, when
exposed to a similar regime of two to four brief (5–20 min) daily sessions all requiring
the performance of a novel behavior, Hou progressively showed more and more
complex behaviors. However, unlike for Malia, some behavioral shaping sessions were
needed in intervening sessions. In particular, in the initial sessions, any given behav-
ior that was reinforced was offered repeatedly by Hou; each session began with the
behavior that had been reinforced in the previous session, but, when that was consis-
tently not reinforced, Hou often fell back into a highly repetitive pattern of leaping in
and out of the water (porpoising), circling, and inverting. To interrupt this repetitive
fall-back pattern, Hou was shaped and reinforced to show a “tail walk” and, in later
sessions, to show a “tail wave.” Thereafter, Hou began to show increasing variety in the
number of behaviors shown per session, including also the number of novel behaviors
she demonstrated. Whereas before Session 16, Hou never emitted more than one new
behavior per session, in Session 16 four completely new behaviors were shown.
In addition, although some sessions occurred with no judged new responses11 (and
thus also no reinforcement), by Sessions 31 and 32, Hou gave entirely novel responses
at the beginning of each of six of seven consecutive sessions and showed no unrein-
forceable responses once that novel response was provided.
This “establishment of a series of new types of responses,” each newly produced at
the beginning of the sessions, was considered to be the end of the experiment:
It appears to demonstrate that the animal had established a class of responses charac-
terized by the description “only new kinds of responses will be reinforced.” After 32
training sessions, the topography of Hou’s aerial responses “became so complex that,
while undoubtedly novel, the behaviors exceeded the powers of the observers to dis-
criminate and describe them” (Pryor et al., 1969, p. 654). Some of the behaviors were
ones that have been found to occur spontaneously in many species (breaching, inverted
swimming, tail slap, sideswipe); others are rarely if ever shown spontaneously, though
they can be shaped (beaching, inverted tail slap, spitting); and still others have never
been observed to occur spontaneously (corkscrew, back flip, inverted leap).
Although these two sets of studies, exploring the effects of reinforcing variability
of behavior in young children and a nonhuman animal species, are different from one
another in many ways, they are similar in that, in both studies, providing positive
reinforcement for generating new and different rather than repeated actions led to a
marked increase in the variability of the behaviors observed. This outcome is both
theoretically and practically important, in that it shows a clear positive or beneficial
effect of reinforcement that is often overlooked.
The effectiveness of reinforcement of variability has been demonstrated in several
other studies, often using highly controlled and precisely measured dimensions of
behavior, such as the interresponse interval between pecks in pigeons (e.g., Blough,
1966; Machado, 1989, 1992), or the sequence of right versus left key pecks (e.g., Page
& Neuringer, 1985; Shimp, 1967),12 and the duration of lever presses in rats (Roberts
& Gharib, 2006). These animal studies have further shown that the level of variable
responding, just as is true for repeated responding, can be brought under discrimina-
tive stimulus control, such that the animal demonstrates variable responding in the
224 M O T I VAT I O N A N D E M O T I O N
presence of one stimulus, but repeated responses in the presence of a different stimu-
lus (Page & Neuringer, 1985). For example, Mercado and colleagues (1998) report on
two bottle-nosed dolphins who were trained to self-select behaviors in response to a
gestured “be creative” command; the animals were permitted to perform any behavior
in response to the “be creative” command, except for behaviors that they had recently
generated in response to the command. One of the animals generated as many as 61
different behaviors in response to the command; the other varied across a range of 88
different behaviors. Investigations have also shown that the degree of variation can
itself be modulated with reinforcement, such that the more variability required to
obtain a reinforcer, the more variable the responding shown (e.g., Machado, 1989;
Page & Neuringer, 1985; K. Wagner & Neuringer, 2006). More recently, reinforcement
of novel behaviors was shown to elicit a wide range of novel vocalized sounds, both
under water and in air, by two captive walruses (Schusterman & Reichmuth, 2008).
B E Y O N D T H E T R A I N E D B E H AV I O R : I M P L I C AT I O N S
F O R P R O B L E M S O LV I N G
These and other studies that have extended the investigation of the effects of rein-
forcement of variable behaviors to additional human populations, such as adolescents
or children with autism (e.g., R. Lee, McComas, & Jawor, 2002; N. Miller & Neuringer,
2000) or individuals with mild depression (Hopkinson & Neuringer, 2003), also raise
hopes for increased modifiability of behaviors that extend beyond the behaviors that
are themselves trained. Such generalized variability is important because it may facili-
tate the acquisition of new behaviors and behavior sequences (Hopkinson & Neuringer,
2003). Indeed, at a broader, more encompassing level, “learning to vary” is, in part,
what is meant by engagement in diverse activities, in that an “enriched” cognitive and
physical environment both enables and requires varied modes of responding and
behavior. From this perspective, training in variability, like enriched environments,
should lead to improved and more flexible problem-solving performance.
Support for such a connection between behavioral variability and improvements in
problem solving is provided by a study that directly contrasted the problem-solving
abilities of animals that were reinforced for variable responding versus animals that
were not (Neuringer, 2004). One group of laboratory rats (the experimental group)
was introduced to different objects each day and the animals were reinforced for
varying how they interacted with each object. By contrast, a control group of rats
(the yoked group) simply received reinforcement at the same times as rats in the
experimental group, entirely independently of how they behaved. This group thus
received the same number of reinforcements as did the experimental group, but in a
random manner that was not correlated with their activity. A second control group
was simply handled each day and did not receive reinforcement.
After this training period, the rats were individually placed in a room in which there
were 30 different objects—all different from the objects that they had encountered in
the training phase. Hidden within each of the objects was a small pellet of food. The
rats were allowed to freely explore the objects for 20 minutes and to consume any of
the food pellets that they discovered. The key finding was that rats in the experimental
group discovered significantly more of the pellets than did rats in either of the control
Act ion an d M ot iv at ion 225
groups (which did not differ from one another). In addition, the rats in the experimen-
tal group appeared to be bolder, and more willing to explore, than were the rats in
the control groups. Thus, directly reinforcing variable behavior, rather than habitual
or repetitive actions, enhanced the problem-solving skills of the animals in new
situations.
This conclusion was further supported by another study that examined the ability
of animals to learn a complex and difficult sequence of right-left lever presses. Only
animals that had received periodic reinforcement for variable responding concurrently
with the learning of shorter sequences of left-right lever press sequences later learned
the more complex and difficult sequence. Neither control animals given no intermit-
tent reinforcement, nor animals given random intermittent reinforcement, did so
(Neuringer, Deiss, & Olson, 2000). Similarly, in research related to that taken up in
Chapter 11, Luchins and Forgus (1955) found that laboratory animals raised in a
broader, more varied environment, when placed in a new context, showed more
variability in their choices and exploratory behavior than did control animals. When
given the opportunity to explore a new multipath maze, in which all of the paths led
to food, animals that were from an enriched environment took more varied routes
than did those from the control environment. Such increments in varied responding,
if manifested in the real world, also would offer the animals many new opportunities
to learn and find resources, thereby further increasing their cognitive and behavioral
repertoires and enabling more adaptive problem solving in future situations.
From the perspective of instrumental learning, where the aim often is to eventu-
ally elicit and then reinforce a particular complex behavior or sequence of behaviors,
variation in the organism’s responding must be neither too little nor too great. If vari-
ation is extremely high, then an animal might never re-produce or repeat the required
(to-be-rewarded) response. But if variation is too low, then, again, the animal might
never produce the required response. Yet in situations where some behaviors have
been frequently rewarded, variation may be too costly.
When some responses are paying off, an increase in the variability of [the]
form [of the response] will decrease the frequency of reward, because some
responses will be outside the criteria for reward (e.g., in the case of duration,
too short or too long). As the likelihood of reward goes down, there is less to
lose, so the cost of variability goes down. If the cost of variability goes down,
the optimum amount of variability should rise. (Gharib, Derby, & Roberts,
2001, p. 177)
Variable responding is often crucial to the discovery of new modes of thinking and
acting (e.g., D. T. Campbell, 1960). Exploration and “foraging behaviors,” such as those
undertaken by animals in the search for new, more palatable, or more plentiful food
sources, lead to greater variability in the types of responses shown. In contrast, highly
stereotyped responding is elicited most markedly under conditions in which continu-
ous reinforcement is offered and so little exploration or foraging behavior is needed
(Lopatto & Brown, 1994; Lopatto et al., 1998). Correspondingly, it is well documented
that response variability increases under conditions where reinforcement is rare or
absent—including periods of behavioral extinction, in which a previously reinforced
226 M O T I VAT I O N A N D E M O T I O N
behavior is no longer rewarded (e.g., Antonitis, 1951; Neuringer, Kornell, & Olufs,
2001). At such times, when reinforcement occurs only rarely or not at all, previously
learned responses still continue to be made but they are intermixed with a higher
number of novel and more varied responses.
At a more cognitive level, under task conditions that are somewhat unclear or
ambiguous to the participant, the discovery of a response that leads to reinforcement
may elicit a type of confirmation bias (e.g., B. Schwartz, 1982) in which a known
“successful response” (one that is reinforced) is simply repeated, without attempts to
explore if it is necessarily the only possible successful response. Learning to repeat,
including repeating a behavior or sequence of behaviors in a very stereotyped manner,
may be adaptive—at least in the short term—when the contingencies reinforce such
repetition: “Doing precisely what has worked in the past seems like a quite sensible
adaptation to most contingencies in the environment. To the extent that such
actions become automatic, time, effort and attention can be devoted to other things”
(B. Schwartz, 1982, p. 26). Reinforcement can give rise to highly stereotyped func-
tional behavioral units that are also highly efficient, provided that the circumstances
are such that mere repetition of past behavior remains effective. In contrast, under
different circumstances—in which reinforcement is made contingent not on repeated
or stereotyped responses but on novel, not previously produced, or only rarely emitted
responses—then reinforcement can also lead to the emergence and strengthening of
varied and divergent, even entirely unique, responses (Goetz & Baer, 1973; Harding
et al., 2004; Maltzman, 1960).
Thus, a highly relevant analogy can be made between “variability” in the context of
instrumental learning and variability in natural selection. In a detailed consideration
of this analogy, Staddon and Simmelhag (1971; also see D. T. Campbell, 1960)
suggested that the term “principles of behavioral variation” could be used to designate
the diverse set of factors that lead to new, “originating behavior” in situations before
any reinforcement occurs. Included among such factors are past experience in similar
situations (transfer), motivation, stimulus factors (e.g., novel stimuli), and so on.
Staddon and Simmelhag suggested that these “principles of behavioral variation” were
directly comparable to Darwin’s laws of variation; they were “intended to denote not
mere variability, but the organized production of novelty, in the Darwinian sense”
(Staddon & Simmelhag, 1971, p. 17). Yet whereas evolutionary theory has empha-
sized both variation (important to the generation of new genotypes) and selection
(important to choosing among genotypes), research on instrumental learning has
been more “one sided:”
too high, it may never make the right response twice (Gharib, Derby, &
Roberts, 2001, p. 165).
C O N T R O L L I N G ( A N D N OT C O N T R O L L I N G ) B E H AV I O R A L
VA R I AT I O N : E X T I N C T I O N A N D T H E I M M I N E N T
P R E S E N C E O F R E WA R D
As noted, variability of responding typically increases under behavioral extinction,
when reinforcement is withheld, and, more generally, when humans or other animals
experience a “downshift” in the reward value of current reinforcement or options com-
pared to a previously experienced value (Balsam, Deich, Ohyama, & Stokes, 1998).
Under these conditions, both the variety of forms of behaviors that are shown, and
the number of environmental stimuli that are interacted with, increase, as shown, for
instance, in the sequences of responses that are made by laboratory rats, or the hori-
zontal placement of their “nose pokes” into a response slot, and the location of pecks
made by pigeons (e.g., Antonitis, 1951; Carlton, 1962; Eckerman & Lanson, 1969).
Reinforcement withdrawal in the form of extinction has been shown to lead to
increased variation in the duration of responses, the latency and force of responses,
and also the nature of displacement responses that occur (Gharib et al., 2001).
Downshifts in reward also have been shown to lead to increased variability of respond-
ing in humans. Participants who first had been trained to type sequences to earn
points were then allocated to one of three groups: one group experienced a decrease in
reward value, another a complete loss of reward, and a third an increase in reward.
Although all three groups experienced surprising changes in reward, only the first
two, for whom the rewards had been reduced or eliminated (downshifted), showed an
increase in behavioral variability as a result of the shift (Balsam et al., 1998).13
Thus far, we have primarily considered the effects of reinforcement on the
frequency of the given behavior. However, it is well known that other dimensions of
behavior, apart from frequency, also are influenced by reinforcement and by specific
contingencies or patterns of reinforcement. Particularly when reinforcement for a
behavior is made available after a given time interval, or after a given number of
responses (e.g., under what are called fixed-interval or fixed-ratio training schedules),
reinforcement often also changes the energy and speed with which a response is given.
When a possible reinforcer is near, or will be given soon, animals and people respond
more quickly, with more energy, and often also more accurately. It is as though the
reinforcer has an extra “attractive pull” when it is nearer in time—and as we or other
animals “anticipate” its arrival. This anticipation of the reinforcement often leads to a
characteristically shaped sequence of responding, with “dips” and “peaks” in response
frequency that look like a repeated scalloped pattern, such that responses are the most
rapid, the most intense, and the most accurate just before reinforcement is given.
But this then raises an important question. If reinforcement can act to increase
the variability of behavior, making it less stereotyped or predictable—does reinforced
variation of behavior also show this temporally related pattern, such that there is more
accurate and speedier variability of responses just before reinforcement occurs?
Cherot, Jones, and Neuringer (1996) considered a number of factors that
might lead to differential effects of the nearness in time of reinforcement on repeated
228 M O T I VAT I O N A N D E M O T I O N
Notably, it is possible that one of the mechanisms by which extrinsic rewards may
undermine intrinsic motivation is precisely through the reduction of variability in
responding. As B. Schwartz (1982, p. 51) observed, one of the properties that is held
in common by many (highly diverse) intrinsically motivated activities is that activities
of this sort, “as a class, permit novel response properties from occasion to occasion,
and result in novel outcomes.” If, in part, it is precisely such variation that sustains the
performance of these activities, then, if particular sorts of contingent reinforcement
eliminate variation, then reinforcement has undermined a key impetus to the (once
intrinsically rewarding) activity.
I N T E G R AT I N G VA R I A B I L I T Y A N D S TA B I L I T Y :
TO WA R D A G R O U N D E D A G I L I T Y
Two final important caveats: First, the previous sections have emphasized the benefits
that can be derived from the reinforcement of, and increases in, variable responding.
However, it is important not to exclusively emphasize the value of variation in acting,
and to appropriately contextualize claims for the benefits of “learning to vary.” Clearly,
reliance on either repeated responses or variable responses can both be adaptive, depend-
ing on circumstance. This point was also stressed by Wong and Peacock, who similarly
highlighted the importance of allowing stereotypy to develop under conditions where
the high level of efficiency that such stereotypy yields will itself be advantageous:
Given the adaptive value of stereotypy, one need not be overly concerned
with the development of stereotypy in educational settings where efficiency
230 M O T I VAT I O N A N D E M O T I O N
Second, and equally important, within any one complex set of conditions, elements
of both highly overlearned and stereotyped and of more innovative, newly generated,
or constructed behaviors may assume complementary and synergistic roles in contri-
buting to flexibly adaptive behavior and thought. The task-guided and condition-
guided intermixing or interdigitization of automatized components of a task (e.g.,
typing text, spelling, computing simple arithmetic sums) and nonautomatized com-
ponents (e.g., strategic, controlled search and evaluation of responses) may ultimately
lead to the greatest flexibility and potential for creative and innovative response.
In some respects, this proposal is analogous to the proposal of R. Epstein (1991,
1985) that the generativity of behavior, including behavior that is novel, continuous,
and probabilistic, is enhanced by the co-presence of multiple competing repertoires of
behavior: Such repertoires compete with one another and interact over time, with
“new sequences and new topographies” that then can be recombined. In a provoca-
tively titled article, “’Insight in the Pigeon: Antecedents and Determinants of an
Intelligent Performance,” Epstein and colleagues (R. Epstein, Kirshnit, Lanza, &
Rubin, 1984) reported that pigeons which had been trained in the essential subcom-
ponents of a complex task (e.g., to climb and peck at a facsimile of a banana; to push a
box toward a green spot placed at random positions within the experimental cham-
ber) later spontaneously solved a new problem that had never been presented. In the
new task, the pigeons needed to push the box underneath the banana, in order to peck
at it. In each case, the solution was attained rapidly, in the space of about 1–2 minutes.
Pigeons that did not earlier acquire the key components (e.g., they had been trained to
push the box, but not toward a specific location) did not solve the novel problem.
Epstein (1987) reported similar outcomes for a more complex behavior, requiring the
novel interconnection of four components rather than three.
These experiments provide support for the adaptive emergence of novelty from
individual behavior repertoires. Epstein (1987; see also R. Epstein et al., 2008, and
Hixson, 2004) argues that, for this reason, conditions that lead to the activation of
multiple competing repertoires—such as multiple controlling stimuli and, also,
intriguingly, failure, because failure may allow the resurgence of previously dominant
responses—are important to enabling creativity.14 Based on these factors, this
researcher also offered explicit practical advice with regard to how to enhance
creativity, several aspects of which, again, involve immersion in relatively “enriched”
environments, together with conditions that allow for the emergence of variability,
rather than repetition.
Most important “is to capture some of the new that is being generated all the time”
(R. Epstein, 1991, p. 368). Artists and writers carry sketchpads and notebooks for
precisely this purpose. The poet Wallace Stevens, for instance, was always at the ready
Act ion an d M ot iv at ion 231
to capture lines and phrases that might suddenly emerge in his mind, sometimes when
he was at work,15 and more often, when he was walking, at lunchtime, and to and from
his home to the office, a distance of about 2.5 miles. “[Stevens] most always had some
envelopes stuffed in his pocket, and he’d just pull them out and write on the back.
Just walking, he’d say, ‘Wait just a minute, please.’ He’d pull out an envelope. He always
had about a half-dozen in his pocket” (Brazeau, 1983, p. 38).
Additional practical advice offered by Epstein concerns creating the conditions for
the emergence of multiple and competing response repertoires:
Finding conditions under which one can take the time to pay attention to
competing repertoires is also important, and one can enhance the competi-
tion by acquiring new skills and knowledge (thus increasing the number of
repertoires available to compete), by exposing oneself to diverse and chang-
ing situations (roughly, multiple controlling stimuli), and by exposing
oneself to new challenges (and the possibility of extinction-induced resur-
gence). (R. Epstein, 1991, p. 368)
Although Epstein’s experiments with the pigeons still involved relatively simple
behaviors, these demonstrations nonetheless forcefully argue that highly overlearned
and stereotyped behaviors may be recombined to enable innovative, newly generated
flexibly adaptive behavior. M. J. Marr also argued for this essential point:
Marr points to particular examples, such as what he dubs the “compulsive and
complete immersion in numbers and equations of the physicist Richard P. Feynman
and the mathematician Srinivasa Ramanujan” and “the endless practices of the
musician” and asks, “What are the consequences of such persistent, relentless,
compulsive play?” He answers: “the result is a huge behavioral repertoire with complex
units, associative links, and relational frames, all in a rich and deep dynamic blend”
(Marr, 2003, p. 23). Proposing an analogy of a dynamical web of interconnectivity of
skills and knowledge and rules and heuristics, Marr continues:
A largely similar emphasis on the generative and creative potential of multiple com-
ponents of behavior has been proposed, again from a rather different direction, in
developmental psychology, and the emergence of new strategic approaches that
children find in problem-solving situations, such as arithmetic. In this case, however,
the components also have the potential to be subjected to higher order evaluations or
metacognitive assessments, as the child reflects on and becomes aware of his or her
own behaviors and the subcomponents that contribute to that behavior. According to
the “competitive negotiation” account of strategy development proposed by Siegler
(2007), the high levels of variability in strategy use shown by children and others may
itself be adaptive because new strategies in problem solving are often constructed from
subroutines of existing approaches. Further, the likelihood and ease of such cross-
fertilization, of the reconjoining of subroutines from different strategies, is increased
if a number of different strategies have been used recently and thus are relatively active
(Siegler, 2007, p. 108). On this latter interpretation, adaptive choices among strategies
and the discovery of new strategies “are fundamentally interwoven processes”:
These authors argue that strategy discovery arises from what they describe as a
“competitive negotiation between meta-cognitive and associative mechanisms”
(Crowley, Shrager, & Siegler, 1997, p. 462). This is a negotiation between associative
mechanisms, involving largely implicit learned associations or correlations among
tasks, actions, and outcomes and metacognitive knowledge that is potentially verbal-
izable and thus potentially accessible for flexible use in planning, monitoring, and
adjusting behavior. For instance, nearly all first-grade children who first discovered a
new method of addition termed the “min strategy” showed variability in how often
they applied the strategy on later problems. In the min strategy, rather than counting
out both numbers to be added, one counts up only from the larger of the two addends
(as in 2 + 3: counted out as “3, 4, 5” or “4, 5” rather than “1, 2 . . . 3, 4, 5”). The children
who discovered this strategy did not generalize its use perfectly to all later problems.
However, those children who were comparatively better able to explicitly state what
they had done showed more consistent application of the strategy to later problems
(they used it on more than 40% of subsequent counting problems) than did children
who showed little explicit insight into their use of the min strategy (these children
used the approach on fewer than 10% of subsequent problems). Yet the complete set
of behavioral observations was not well accounted for by either metacognitive or
associative mechanisms alone: Both were needed.
Act ion an d M ot iv at ion 233
Crowley and colleagues (1997) propose that the dominance of one system over the
other is largely determined by the extent of experience that the associative system
has. If the problem solver is working in a highly familiar context, then the fast associa-
tive system may dominate, and the metacognitive system may focus, instead, on mon-
itoring progress of the associative system, or notice and encode “interesting aspects or
concomitants of strategies that are not necessarily related to the immediate goal of
solving the problem” (Crowley et al., 1997, p. 480). However, in novel situations, the
metacognitive system may assume a larger role. The metacognitive system may also
intervene at other points, for a variety of reasons, such as “noticing something inter-
esting about prior solutions, becoming tired of using the same approach, perceiving a
time-saving shortcut, or encountering explicit instructions (e.g., from a teacher) about
how to solve a problem” (Crowley et al., 1997, p. 481). Thus, the discovery of new
strategies will not always occur during an impasse, but may occur during the perfor-
mance of quite familiar tasks that allow sufficient leeway for such metacognitive notic-
ing and observation. These conditions may also encourage resistance to acting on
whatever strategy is proposed by the associative system, in deference to a more novel
or stimulating approach. The “negotiation” between the two systems allows for many
degrees of explicit knowledge concerning how and why discoveries occurred. For
example, “Sometimes, a weak bid from the meta-cognitive system will be enough to
nudge the associative system to select a new path” (Crowley et al., 1997, p. 483)—but
the reasons for the resulting strategic change might not be readily verbalized and be
accompanied with little explicit insight.16
Taken together, then, the evidence for our joint ability to learn to vary and to learn
to repeat, and the potential role of metacognitive reflection, affirms the need for mul-
tiple and varied levels of control—as proposed by the iCASA framework. There are
potential benefits and potential drawbacks from both varying our actions and from
repeating our actions; both are necessary, and together they can often compensate for
the shortcomings of the other. Both, together, form a particularly powerful alliance
for creatively adaptive behavior and agility of mind.
Looking Back
In this chapter, we have focused on the diverse ways in which aspects of motivation
and action intersect with cognition to either shape or obstruct agility of mind. We
began by canvassing the benefits and costs of adopting a higher level, more abstract
versus lower level, more concrete construal of “what we are doing” and the relations
between our level of construal and self-regulation. We then turned our attention to
the intersections between automatic and controlled processes in influencing our
ability to both appropriately postpone, and to opportunely resume, our intentions
to undertake particular actions, in accordance with changing contextual circum-
stances, and also as a function of the level of representational specificity at which we
had anticipated possible opportune moments or contexts.
Intersections of motivation and action with several developmental and personality
factors, such as openness to experience, were then emphasized. We considered
questions such as whether it is possible to be too controlled or overly controlled and also
234 M O T I VAT I O N A N D E M O T I O N
the evidence that our capacity for self-regulatory control may be a “limited resource”—
albeit also a capacity that may be extended through exercise. We noted how the
demands on self-regulatory resources may be modified by such factors as whether we
experience what we are doing as predominantly externally imposed or as more freely
chosen or self-determined. This then led us to a consideration of the unipolar rather
than bipolar nature of motivation—such that, for a given behavior or domain,
individuals may be high or low on both intrinsic and extrinsic motivation. Here we also
encountered the important notion that extrinsic motivation, too, comes in different
guises, varying in the level of experienced autonomy (from external regulation,
characterized by the lowest level of autonomy to integrated regulation, characterized
by the most autonomy), with markedly differing consequences for the ways we are
likely to pursue a given action.
In the final several subsections of the chapter we considered especially the effects
of reinforcement on creative and adaptive behavior, such as the question of what types
of rewards can be beneficial for creativity, and the key notion that not only repetitions
of behaviors but also variations of behaviors—including novel and innovative actions—
can be fostered and encouraged through reinforcement. The potential benefits of
variation, and the possible “leaps” in learning that might occur through having a wider
repertoire of subcomponents of behaviors that can be called upon, and recombined,
were highlighted. The chapter closed with theoretical considerations of the roles of
both response variability and response stability in enabling innovative advances in
thought and action.
production, generous access to many excellent dancers, dedicated rehearsal times for
those dancers, and (topping off the list) the vast musical potential provided by an
entire and talented orchestra.
All this, though, Tharp underscores is something she immediately should
have identified as a source of imminent danger, and that should have quickly placed
her on “red alert.” In her wonderfully designed book, the message that she should
have heeded appears in large red font, blazoning forth from the surrounding land-
scape of smaller black text: “Whom the gods wish to destroy, they give unlimited
resources” (p. 129).
Why the red alert—and that in the face of such a windfall of good things?
Because, because: creativity rarely occurs in an unconstrained and entirely
open-ended unbounded universe—or, if it does, the creator’s first act may be to inten-
tionally and freely impose constraints where none necessarily existed. Think of Piet
Mondrian’s later palette of “primary” colors and his exclusive use of straight lines and
planes. Think of Agnes Martin’s resolute sparseness: “My paintings have neither
objects, nor space, nor time, not anything—no forms” (Cooke, 2005, p. 27); or of
Barnett Newman’s recurrent (but never the same) upward reaching “zips,” simultane-
ously spanning, defining, and defying the canvas. Each of these artists both found and
made a more limited “micro-world”—or micro-language—with its own syntax, and its
own vocabulary. . . to allow vast generative (and regenerative) creativity.
Unlimited resources are, from this perspective, somewhat akin to a universe with
no known vocabulary, no known means of expression. Unlimited resources may
remove the very constraints that provide an important channeling, directing, and
guiding force for creative energy—constraints that free and unleash creativity rather
than hamper it by providing initial boundaries and limits to work within and around
and against. It is notable that the artist Jeff Wall spoke of “renunciation,” such as the
renunciation of color as an “originary gesture” (Wall, 2005a)—to be creative means to
forgo some options or courses for others.
The cognitive psychologist Thomas Ward (1994) has described what may occur in
situations where there are few constraints operating as taking the “path-of-least-resis-
tance.” Unfortunately, taking this path often will lead us to simply implement the first
solution that comes to mind. Yet that solution is itself likely to be based on a solution
that worked in the past, or on largely habit-bound semantic memory processes, such
as category generation, and thus is unlikely to be either particularly innovative or
uniquely tailored to the specific circumstances at hand.
The conditions that foster agile thought arise from the dynamic interaction between
automatic processes, such as reminding and semantic association, and nonautomatic
processes, such as deliberate search, a willingness to tolerate and “enjoy” uncertainty
or ambiguity, where the materials or situation at hand preclude the simple application
of a simple “straight out of the box”—or “out of the past”—solution. Agile thought
also often may depend on the self-generation of constraints and constraints that vary: a
self-imposed demand for variable responding (for experimental and theoretical review,
see, for example, Moreau and Dahl, 2005, and P. D. Stokes, 2001).
Further, it seemed that, in Tharp’s (richly illustrative!) case, circumstances
conspired not only to remove or make it more difficult to either make or choose this
would-be source of intrinsic motivation consisting of the challenge of meeting known
236 M O T I VAT I O N A N D E M O T I O N
238
E motio n , S e l f, Pe rs on al it y 239
Positive Emotions
W H AT I S T H E F U N C T I O N A L R O L E O F P O S I T I V E E M OT I O N S ?
Positive emotions can play an important role in promoting agile thinking. However,
not all positive emotions are of the “same ilk” but may differ substantially depending
on the type of action situation from which they emerge (e.g., Carver & Scheier, 1990;
Higgins, 1997). One broad group of positive emotions may arise from the successful
avoidance of negative outcomes or events—these might be emotions such as relief, or
calmness, or tranquility (rather than the contrary states of fear, tension, anxiety, and
so on). These are positive emotions that often arise in the context of the actions of
escaping from, eluding, or avoiding threats. In contrast, another broad group of posi-
tive emotions may arise in the context of pursuing incentives: typical positive emo-
tions in this approach context are eagerness, excitement, or joy.
Carver (2003, 2004, 2006) has argued that affect often provides a source of feed-
back regarding whether our activities are leading us closer to our goals. Positive affect
indicates good, or better-than-expected progress toward the goal, whereas negative
affect points to poor, or worse-than-expected goal-related progress. Thus, if our activ-
ities are going well, then we are likely to experience pleasure, but the type of pleasure
will vary depending on whether the action we are engaging in is one of avoidance or
approach. Both types of action can lead to positive affects, to neutral affect, or to
negative affect, but on different continuums, ranging from fear and anxiety (negative
pole) to relief and calmness (positive pole) for actions aimed at avoidance, but sadness
and depression (negative pole) versus elation and eagerness (positive pole) for
approach actions.
In Carver’s model, it is comparatively easy to understand the role of negative affect.
Negative feelings indicate that something is not going well, and so we (typically) will
try harder or undertake a different approach to the matter at hand. What is counter-
intuitive, in the model, is what happens when positive feelings occur, because things
are going “better than they need to.” In this case, individuals may begin to “coast” a
bit—letting up on their efforts with regard to the particular activity.
This seems paradoxical, and even contrary, to claims that pleasure in an activity
should lead to an intensification of engagement in the activity. Yet the latter
proposal (pleasure intensifies engagement) itself raises a problem: If pleasure leads to
240 M O T I VAT I O N A N D E M O T I O N
Doing Openness to
other goals
well Elation
Coasting,
Positive
conserving
energy
Activation,
Eagerness
Criterion to sustain
velocity
Frustration
Activation,
Anger to regain
Negative
velocity
Sadness
Depression Deactivation,
Doing in service of
poorly Dejection disengagement,
conservation
Despondency of energy
Engagement
track training in the prior weeks (associated with nearness of the goal of qualifying for
the event) or had been doing consistently poorly (associated with distance from the
qualifying goal). They were then also asked to imagine that they had just been to a
further training session in which they achieved either a winning time in all 12 trials or
had obtained a bad time in all 12 trials. This further manipulation was intended to
influence positive versus negative emotion, and it was crossed with the manipulation
of goal distance, so that four goal distance by emotion conditions were created:
near–positive, near–negative, distant–positive, and distant–negative.
The results showed that, when the goal was near, positive emotions increased the
extent to which participants were likely to “choose” to decrease—not increase—their
training efforts in order to meet the additional financial goal. In contrast, negative
emotions under these conditions instead increased the effort devoted to the focal goal
242 M O T I VAT I O N A N D E M O T I O N
and participants chose to exert less effort toward earning extra money. Additional
findings from these investigators likewise supported the notion that when “focal goal
attainment is imminent and goal-related emotions signal progress” individuals
with multiple goals tend to reduce their efforts toward the goal and also then begin to
“prioritize competing goals” (Louro et al., 2007, p. 191).
More generally, positive affect may encourage us to deepen and broaden how we
interact with the world and with other people so that we engage in additional explora-
tion and attempts to understand social and physical events, rather than simply auto-
matically or habitually reacting to those events. Positive affect may encourage social
interactions (e.g., Cunningham, 1988; Vittengl & Holt, 1998; D. Watson et al., 1992)
and may help to foster cooperative or helping behavior (e.g., George & Brief, 1992;
Isen, 1987). Diary studies show that high levels of positive affect, as reported in daily
or weekly logs, are associated both with higher levels of social activity (e.g., time with
friends, family, or partners) and an increased frequency of engaging in a variety of
leisure and other activities (e.g., going to a museum, arts or hobbies, weekend trips,
etc., e.g., D. Watson et al., 1992). Further, individuals who are happy are more likely to
actually enjoy themselves when engaging in such leisure activities than are less happy
individuals (e.g., L. Lu & Argyle, 1991), and they have a greater likelihood of experi-
encing intrinsically rewarding states (Graef, Csikszentmihalyi, & Gianinno, 1983).
These findings suggest that there may be incremental longer term consequences of
more often experiencing states of high positive affect. Individuals who tend to experi-
ence positive affect across many situations over an extended period of time or who are
high scorers on positive affect as a personality trait may engage in activities and affili-
ations that themselves further foster positive affect. In turn, such engagement may
increase both the positive nature of their experience and the breadth of their cognitive
horizons in ways that further enable creative approaches to problems and problematic
situations (e.g., Fredrickson & Joiner, 2002; Tugade & Fredrickson, 2004).
This self-reinforcing process, whereby positive emotional experiences give
rise to “reachings-out” into the world and toward others in ways that then supplement
and extend our knowledge has been termed the “broaden and build theory.” According
to broaden and build theory (Fredrickson, 1998, 2001, 2004), the exploration,
modification, and extension of our understanding and skills is most likely to occur
when we are in a positive emotional state, such as interest, or contentment. That is, it
is especially such positive emotions that “appear to broaden peoples’ momentary
thought-action repertoires and build their enduring personal resources” (Fredrickson,
2004, p. 1369).
In brief, according to the broaden and build account, “over time and as a product of
recurrent play, exploration, and integration, positive emotions have the incidental
effect of building a person’s social, physical, and personal resources (e.g., recurrent
exploration increases a person’s knowledge base)” (Kunzmann, Stange, & Jordan,
2005, p. 575). Other researchers have made similar claims. For example, Lyubomirsky,
King, and Diener (2005, pp. 803–804) point to research that “positively valenced
moods and emotions lead people to think, feel, and act in ways that promote
both resource building and involvement with approach goals” (e.g., Carver, 2003;
Elliot & Thrash, 2002; Lyubomirsky, 2001). These views are also at least broadly
consistent with the “feelings-as-information” model (e.g., N. Schwartz, 1990, 2001)
E motio n , S e l f, Pe rs on al it y 243
and its construal of the “signal” that is provided by positive affective states versus
negative affective states. According to this view, whereas negative affective states
signal that the current state may be problematic, and are associated with increased
aversion to risk and the inhibition of the use of novel alternatives, positive affective
states signal safety. On the “feelings-as-information” model, situations invoking
positive affect suggest that cognitive effort is unnecessary unless required by other
ongoing goals or aims. Such positive affective states also tend to be associated with an
increased tendency toward risk taking and the exploration and use of novel or creative
alternatives.
such nontypical items during a category generation task (Hirt, Levine, McDonald, &
Melton, 1997).
Positive affect has also been associated with enhanced fluency on the Alternative
Uses Task, requiring the generation of nonstandard uses of common objects (Phillips,
Bull, Adams, & Fraser, 2002), as well as with facilitated performance on more complex
measures of divergent thinking (Vosburg, 1998). In other research, the induction of
positive affect led to the formation of both broader and thus fewer categories when
individuals were encouraged to focus on the similarities among exemplars, but
narrower and more numerous categories when they were encouraged to attend to
differences among exemplars (N. Murray et al., 1990).
The latter outcomes suggest that positive affect might enhance an individual’s
ability to perceive less salient or less common characteristics or relations. This sugges-
tion is consistent with a further demonstration by Isen and colleagues (Isen, Daubman,
& Nowicki, 1987) of the effects of positive affect on thinking. In this case, however,
what was measured following the induction of a positive affective state, or in several
control conditions, was the participant’s ability to solve Duncker’s “candle problem.”
As discussed in Chapter 4, in relation to issues of perceptual attunement and the
influence of the “design stance” on categorization and problem solving, Duncker’s
candle problem involves the presentation of several objects, including some tacks, a
box, a candle, and (in some versions of the task) a vertical screen. Participants are
asked to use these materials to affix the candle to the vertical screen, so that it can
burn upright. This proves to be a difficult task because, in the standard condition, it
requires changing how one sees the box: When it is currently being used as a container
of the tacks, the solution to the problem requires emptying the box of the tacks and
using the box to support the candle.
Isen et al. (1987) found that only 3 out 15 control participants who watched a neu-
tral film prior to being given the candle problem managed to solve the problem within
the 10 minutes allotted to do so; this performance level was similar to that shown by
participants in a no manipulation control condition, where 2 out 15 participants
solved the problem. In marked contrast, for participants shown a positive (comedy)
film, 9 out of 12 solved the problem. Indeed, the participants in the positive film
condition demonstrated a solution rate that was nearly as high as that of participants
who were presented the problem with a visually facilitative display, such that all of the
objects were separated from one another, with the tacks beside the box rather than
inside the box. (See also the discussion in Chapter 4, of the differential effects of
“preutilization” or function priming on the performance of younger vs. older children,
with younger children tending to be less adversely affected by the current usage of the
objects than are older children.)
Positive affect arising from watching a comedy film also has been shown to facili-
tate conceptual-associative problem solving (Estrada et al., 1994; Isen et al., 1987;
Subramaniam, Kounios, et al., 2009) on the “remote associates task” (Mednick, 1962).
In the remote associates task, three different words, each of which is associatively
related to a further word, are presented. The participant’s task is to identify the word
that connects all three presented words. For example, the three stimulus words, age,
mile, and sand, are all related to the target word, stone. Enhanced semantic associative
search on the remote associates task for individuals given a positive compared with a
E motio n , S e l f, Pe rs on al it y 245
negative mood induction was also found using a music induction procedure, in which
individuals initially listened to either 10 minutes of music that had previously been
shown to induce a more positive mood, or to 10 minutes of music known to induce a
more sad mood, and then continued to be softly exposed to the happy or sad music
throughout the remainder of the test period (G. Rowe, Hirsh, & Anderson, 2007;
Chapter 9 considers some of the possible neural factors that may facilitate perfor-
mance on this task).
Individuals in a positive mood may also provide more unusual word associations
than do persons in neutral or negative affect conditions. This pattern held for each of
three different definitions of “unusualness,” including a measure comparing the
responses to those given in a normative sample of 1,000 respondents (Isen, Johnson,
Mertz, & Robinson, 1985). These experimental results also are in line with psycho-
metric findings concerning the cognitive characteristics that are associated with
elevated positive mood, and also with findings relating to the cognitive effects of mild
hypomanic states, in which individuals may show symptoms similar to those found in
mania, but less severe. In addition to elevated mood, such individuals may, for exam-
ple, show decreased need for sleep and high levels of energy but also tendencies toward
overinclusiveness of thinking and a loosening of conceptual boundaries (C. L. Bowden,
1994; Richards, 1994).
Mild hypomania may be associated with higher levels of fluency of ideas or diver-
gent thinking (Furnham et al., 2008) and associative and combinatorial thinking,
including the intrusion of irrelevant ideas or incongruent combinations (Jamison
et al., 1980; Schuldberg, 2000-2001). Several researchers have pointed to the similar-
ity between episodes involving mild hypomania and intense phases of creative
endeavor. Richards (1994, pp. 56–57) observed that the cognitive style in mild hypo-
mania is one of “integrative complexity” (cf. Barron, 1963), and that a “preference for
the complex integration of material is an important associate of creative thought
across different fields of endeavor.” She further identified three specific effects of
mood, and of mood swings, that might “raise the odds for the emergence of creative
thoughts.” These are, first, “the number of available elements or classes” available to
awareness; second, “the richness and sophistication of their structural intercombina-
tions”; and, third, “the flexibility of their dynamic patterns of access and use (at least,
if central cognitive control is retained and not abandoned for a psychotic process).”
In a study using a university-wide behavior inventory to identify students who
might be at high risk for bipolar syndromes, P. J. Shapiro and Weisberg (1999) found
that symptoms relating to hypomania or euphoria were significantly positively
correlated with scores on the adjective checklist creative personality scale (ACL-CPS,
Gough, 1979). Persons who displayed a “hyperthymic” pattern involving high levels of
(subsyndromal) mildly elevated mood with few or no symptoms of depression scored
significantly higher on the creativity measure than did individuals showing either
depression or a cycling pattern (cyclothymia). Using multiple regression analyses,
hypomania symptoms were again related to creativity; although depressive symptoms
alone were not predictive of creativity, the combination of hypomania and depression
dimensions accounted for the largest proportion of variance in the adjective checklist
measure of creativity, leading the authors to suggest that “depressive symptomato-
logy has a suppressive effect on creativity” (P. J. Shapiro & Weisberg, 1999, p. 757).
246 M O T I VAT I O N A N D E M O T I O N
Similarly, in earlier work, Schuldberg (1990) found that hypomanic personality traits,
measured by a scale concerning experiences of being “up” or “hyper,” were positively
correlated with the adjective checklist measure of creativity and with creative scores
on the Alternative Uses Task, as well as with a questionnaire of beliefs, attitudes,
traits, and behaviors associated with creativity. As observed by Kaufmann (2003,
p. 132), “in a positive sense, this cluster of cognitive characteristics may tend to
facilitate originality and creativity in problem solving.”
A further demonstration of the beneficial effects of mild positive affect for agile
thinking— in this case involving decision making and reasoning in physicians—is that
provided by Estrada, Isen, and Young (1997). In this study, internists were randomly
assigned to one of three groups: a mild positive affect group (given a small gift of
candy), a control group, or a further comparison condition. The physicians were asked
to read a summary of a case of a patient, and then to “think aloud” while they attempted
to determine a diagnosis. During their attempted diagnosis, they could choose to read
different sorts of information about the patient, and they also could request the results
of various lab tests. The physicians’ think-aloud protocols were tape-recorded and then
later transcribed and scored for several features. The researchers focused particularly
on evidence pertaining to the point in time at which the correct diagnosis was
first suggested, evidence for engaging in a process of hypothesis confirmation, and
indicators of “anchoring,” here defined as involving an overly strong and continued
adherence to an early hypothesis rather than considering alternative hypotheses.
The mild positive affect and control groups established a final diagnosis at a similar
point in the protocol (hypothesis confirmation), and all physicians did so only with
sufficient evidence; that is, no physicians decided on a diagnosis prematurely. However,
physicians in the mild positive affect condition generated the correct hypothesis
(hypothesis generation) and began to consider the correct diagnosis significantly
earlier in the protocol than did those in the control group. The positive affect group
also showed less “anchoring” on an initial hypothesis than did the control group. Thus,
the earlier generation of the correct hypothesis in the positive affect group did not
reflect hasty or closed responding, but points to relatively enhanced “efficiency,
improved integration of material and improved correct hypothesis generation”
(Estrada et al., 1997, p. 131).
The beneficial effects of positive affect on problem solving may not be confined to
situations where individuals face problems on their own—some findings suggest that
positive affect also enhances interpersonal problem solving. Using an interpersonal
bargaining task, Carnevale and Isen (1986) found that individuals in a positive affect
exposure condition negotiated more effectively and achieved solutions that had higher
joint benefits than did control participants. There is also evidence that, compared with
a relatively negative naturally occurring affective state, positive mood may be related
to increased fluency of ideas both with regard to proposing possible approaches or
solutions to everyday problem scenarios, and for the process of envisioning possible
productive questions to pursue, or “problem finding” (Okuda, Runco, & Berger, 1991)
requiring the identification of problems of a given broad type (Vosburg, 1998).
Isen and her colleagues suggest that the beneficial effects of positive affect on
creative problem solving arise from alternations in an individual’s attentional focus
that accompany the changes in affective state:
E motio n , S e l f, Pe rs on al it y 247
The interpretation that we have suggested for the impact of positive affect
on creative problem solving is that good feelings increase the tendency to
combine material in new ways and to see relatedness between divergent
stimuli. We hypothesize that this occurs because the large amount of cogni-
tive material cued by the positive affective state results in defocused atten-
tion, and the more complex cognitive context thus experienced by persons
who are feeling happy allows them a greater number and range of interpreta-
tions. This increased range of interpretations results in awareness of more
aspects of stimuli and more possible ways of relating and combining them.
(Isen, Daubman, & Nowicki, 1987, p. 1130)
However, as also noted by these authors, the directionality of some of the effects
remains unclear. For example, do individuals in a more positive affective state notice
more features because they are aware of more alternative interpretations, or are they
more aware of alternative interpretations because they notice more features?
Nonetheless, a somewhat similar account, emphasizing the increased “breadth” of
activation of cognitive and memory-based associations during positive affective
states, has been proposed by other researchers. For instance, according to what has
been termed the “personality systems interaction theory,” proposed by Kuhl and asso-
ciates (Kuhl & Kazén, 1999), affective states influence (modulate) the ease and type of
associations that individuals make. This account proposes that positive affect sup-
ports a holistic processing mode, associated with the “activation of wide semantic
fields” in memory and thus encompassing weak or remote associates, whereas nega-
tive affect supports analytic processing and is characterized by a “more restricted
spread of activation to close associates and dominant word meanings” (Bolte, Goschke,
& Kuhl, 2003, p. 416; see also the section on “Brain Correlates of Insight Problem
Solving” in Chapter 9, including Figure 9.6).
According to this account, although mild positive affect may be associated with a
preference for global processing, this does not entail a reduced ability to flexibly switch
to more local strategies if conditions so require. The personality systems interaction
theory proposes that positive affect enhances “open, flexible and efficient processing.”
More specifically, this theory postulates that positive affect increases the accessibility
of a high-level intuitive form of memory, termed “extension memory.” As summarized
by Baumann and Kuhl (2005):
Evidence in line with this flexibility hypothesis was provided by an initial experiment
that manipulated mood via a trial-by-trial priming manipulation (Baumann & Kuhl,
2005). The experiment used a perceptual identification task where the stimuli were
larger geometrical objects composed of smaller geometrical objects. Participants were
required to detect a given target shape (e.g., a triangle) that could be present in either
the global form or the local form (e.g., a large circle constituted by many smaller trian-
gles). Each trial was preceded by a priming word that, for the individual participant, was
associated with neutral, positive, or negative affect. Based on participants’ responses
following the neutral word primes, individuals were classified as either showing a global
processing default bias (about two-thirds of the participants) or a local processing
default bias (one-third of the participants). The results showed that, for the “global
default group,” positive primes reduced latencies to nondominant local targets. However,
the reverse occurred for the “local default group”—that is, for this group, positive affect
facilitated processing of global targets. In contrast, negative affect primes did not influ-
ence processing of global targets and slowed responding to local targets. These outcomes
suggest that positive affect may enhance not only the processing of global information
but also (at least under some conditions) the processing of local information if situa-
tional demands require a focus on such detailed information. They are, then, conceptu-
ally consistent with the results reported by N. Murray et al. (1990), and considered both
earlier in this section and in Chapter 3, that a positive affective state led individuals to
show more flexible categorizations than did participants not in a positive affective state,
not only forming broader and thus fewer categories when asked to focus on the simi-
larities among exemplars but also forming narrower and thus a greater number of cat-
egories when instead asked to focus on differences among exemplars.
positive mood supports the creative function of active generation, or enriching the
stimulus input with inferences based on prior knowledge.” Similarly, Clore and Palmer
(2009, p. 26) proposed that affect is one factor governing the “tipping point” between
perceptually focused bottom-up processing versus cognitively focused top-down
processing, with positive affective cues promoting cognitive, relational processing and
negative affect encouraging a more perceptual, stimulus-bound focus. It also has been
suggested that negative affective states may signal that one’s dominant response
should not be given (that is, one should avoid the use of accessible cognitions and
responses), whereas positive affective states encourage the provision of dominant
responses (Clore & Huntsinger, 2007). In a similar vein, Bless (2000, p. 213) suggested
that it may be “highly adaptive for individuals to rely on their general knowledge
structures differentially as a function of the current psychological situation”—such
that individuals “in benign situations may rely on their general knowledge structures,
which usually serve them well,” whereas in problematic situations, which are usually
deviations from normal or routine circumstances, individuals “would be poorly advised
to rely on the knowledge they usually apply.”
Evidence that is apparently consistent with the latter suggestions has been
reported. For instance, persons in a positive mood who were asked to make “first
impression” judgments of others were more strongly influenced by irrelevant “primes”
than were the judgments given by persons in a negative mood (Fiedler et al., 1991).
Similarly, positive mood participants were more prone to the effects of “misleading
postevent questioning” than were persons in either a neutral or negative mood
(Forgas, Laham, & Vargas, 2005). They were also more prone to incorrectly recall asso-
ciatively related words in a word-learning task (Storbeck & Clore, 2005), possibly
because positive mood increased a tendency to accept information in an uncritical,
accepting manner (e.g., Bless, 2000) or increased reliance on relational rather than
item-specific processing (e.g., Storbeck & Clore, 2005).
Other studies have shown that participants in positive moods may be less influ-
enced by argument strength than by peripheral cues (e.g., Bless, Mackie, & Schwarz,
1992), and they also show greater reliance on stereotypes in their judgments (e.g.,
Bodenhausen, 1993; Stroessner & Mackie, 1992). Also, for individuals in a negative
mood, task instructions that directly and explicitly encourage them to provide
responses freely have been shown to lead to greater fluency, particularly for new
responses (Gasper, 2004). This outcome suggests that the diminished fluency of new
ideas observed in individuals with negative affect may at least partially be attributable
to their adoption of a more stringent criterion for “outputting” a response that then
leads to the “editing out” or suppression of generated ideas rather than the failure to
have such ideas at all.
Further findings pointing to rather less than universally positive benefits from
positive mood also have been reported. Two studies by Kaufmann and Vosburg (1997,
2002) failed to show benefits of positive mood on insight problems, and indeed,
showed that positive mood impeded performance. The second of these investigations
provided evidence that the beneficial effects of positive mood on the fluency of idea
generation may be predominantly found early on in the phase of generating ideas but
that, over time, idea production by individuals in a neutral or negative mood exceeded
that of individuals in a positive mood. It also has been suggested (Vosburg, 1998) that
250 M O T I VAT I O N A N D E M O T I O N
these conflicting findings may be related to the types of task constraints that are
present, specifically whether successful task performance requires systematic search
and “optimizing” versus heuristic search and “satisficing.” In the insight problem task
of Kaufmann and Vosburg (1997), participants were not provided feedback as to the
adequacy of their solutions, and it is possible that a positive mood led individuals to
stop sooner with a solution that they believed to be sufficient, but not the one deemed
“correct.”
Yet from this perspective, according to which positive moods lead to processing
that is more reliant on heuristics and prior knowledge, it is difficult to understand
the bidirectional facilitative categorization effects that have been reported by
N. Murray et al. (1990; also compare with the findings regarding the local/global task
of Baumann & Kuhl, 2005, discussed in the previous section). As noted earlier,
N. Murray et al. (1990) found that a positive affective state led individuals both to
form broader categories when asked to focus on the similarities among exemplars and
to form narrower categories when instead asked to focus on differences among
exemplars. It seems unclear why greater reliance on preexisting general knowledge
structures would not instead have led to stereotyped or habitual responses. Likewise,
the findings from Estrada, Isen, and Young (1997), showing that physicians in a posi-
tive mood manifested comparatively less anchoring on an initial hypothesis than did
those in a control group, also do not seem to cohere well with the proposal that posi-
tive moods necessarily lead to more heuristically or schematically driven processing.
Taken as a whole, whereas there is a good deal of evidence supporting the potential
facilitative effects of positive moods on creatively adaptive thinking, there are also a
number of empirical findings that clearly raise the need for caution in making overly
encompassing and unilaterally enthusiastic statements regarding the effects of posi-
tive affect on cognition (see also Hennessey & Amabile, 2010). Furthermore, the
observation of beneficial effects for modest positive affect on creatively adaptive think-
ing should not be taken to indicate an exclusivity claim—other forms of affect, such as
emotional ambivalence, might also sometimes prove beneficial (e.g., Fong, 2006). A
fuller understanding of the contributions of positive affect to mental agility will need
to take into account several factors. Prominent among these are the questions of how
well the cognitive effects of mild positive affect “match” the predominant demands of
a given problem situation—such as predominantly favoring local versus global pro-
cessing, or maintaining goals versus flexibly switching goals—and whether an increased
openness or orientation to novelty may, under a given set of task or situational circum-
stances, be beneficial or harmful (e.g., Dreisbach, 2006; Dreisbach & Goschke, 2004;
Phillips et al., 2002; see also Förster & Dannenberg, 2010, for extended discussion).
Nonetheless, and also taken as a whole, the majority of the research to date indi-
cates that, at least under a number of task conditions, positive affect plays an impor-
tant facilitative role in flexible thinking. This facilitation arises, in the first instance,
through comparatively immediate short-term effects on cognitive processing (e.g., in
altering the ease with which categories are extended to include atypical members).
More speculatively, in a longer term manner, such facilitation may emerge because
positive affect helps to “broaden and build” (e.g., Fredrickson, 1998, 2001) an
individual’s repertoire of problem-related skills and knowledge that, in turn, enhance
creatively adaptive thought. As we will see in the next section, there is also evidence
E motio n , S e l f, Pe rs on al it y 251
P O S I T I V E E M OT I O N , P S Y C H O L O G I C A L R E S I L I E N C E ,
A N D T H E “ G R A N U L A R I T Y ” O F E M OT I O N S
Broadly stated, psychological resilience involves an ability to “bounce back” from nega-
tive emotional experiences and to flexibly adapt to the changing demands imposed by
stressful situations or events. Resilience is demonstrated by the effective coping and
adaptation of an individual, even though he or she is confronted with varying degrees
of stress, including loss, hardship, or adversity (also see the second section of Chapter
5, particularly the subsections on “Ego Control and Ego Resiliency” and “Effortful
Control and Reactive Control”). Research has shown that “trait-resilient” individuals
tend to share many characteristics: They are generally optimistic and full of energy,
curious and open to new experiences, and—most relevant here—tend to show high
levels of positive emotionality (e.g., J. Block & Kremen, 1996; Klohnen, 1996).
Positive emotions may help to bolster and sustain psychological resilience by
“undoing” the lingering aftereffects of negative emotions and helping to restore an
individual to physiological (e.g., cardiovascular) and psychological equilibrium. In one
study (Fredrickson & Levenson, 1998) participants were first asked to watch a fear-
eliciting film, and then were asked to watch one of four further films intended to elicit
contentment, amusement, or sadness, or to be emotionally neutral. Individuals who
watched either the contentment or amusement films showed faster recovery to base-
line cardiovascular reactivity after the fear-eliciting film than did individuals who
watched the sad or neutral film. Fredrickson and Levenson (1998) further found that
those participants who spontaneously smiled while they were watching a sad film
showed a more rapid return to baseline levels of cardiovascular activity than did
participants who did not smile—suggesting a possible buffering effect of spontaneous
positive emotion.
In other work, Ulrich et al. (1991) likewise found evidence for more rapid physio-
logical recovery, and also recuperation of self-rated affect, from a laboratory-induced
stressor after exposure to (pleasant) nature scenes than to (less pleasant) urban
scenes. Partly based in psycho-evolutionary theory (e.g., Parsons et al., 1998; Ulrich,
1993; Ulrich et al., 1991, 2008) and E. O. Wilson’s (1984) concept of “biophilia” (a love
of living things), Ulrich proposes that exposure to particular sorts of natural scenes
may both counteract negative affect and foster positive affect. According to this
account, often beginning with “immediate, unconsciously triggered and initiated
emotional responses” (1991, p. 207), natural settings favorable to ongoing well-being
and survival (e.g., a savannah-like area or a setting with water), rapidly help to offset
or counter stressors. Such settings may shift us toward a more positively toned
emotional state, counteract stress-induced mobilization of the sympathetic nervous
system (e.g., elevated blood pressure and electrodermal activity) and influence
attention, subsequent conscious processing, and behavior. (Chapter 11 will consider
additional experimental research documenting the beneficial effects of exposure to
nature on directed attention capacity.)
252 M O T I VAT I O N A N D E M O T I O N
Links between positive affect and psychological resilience have also been reported
when using questionnaire measures to assess more stable “trait” resilience. Using
J. Block and Kremen’s (1996) Ego-Resiliency Scale, consisting of 14 self-reported items
such as “I quickly get over and recover from being startled” and “I enjoy dealing with
new and unusual situations,” Tugade, Fredrickson, and Barrett (2004; Tugade &
Fredrickson, 2004) found that psychological trait resilience was positively associated
with positive mood but was not associated with negative mood. They also showed that
resilient individuals recovered from the cardiovascular effects of anxiety (experimen-
tally induced through telling participants that they would be given 60 seconds to
prepare a 3-minute speech on a still-to-be-determined topic) more quickly than did
less resilient individuals. Furthermore, using R. M. Baron and Kenny’s (1986) criteria
for establishing statistical mediation, these researchers found that the relation
between the duration of cardiovascular reactivity and resilience was mediated by
positive emotion: The relation between physiological reactivity and resilience was no
longer significant when controlling for positive emotionality.
Nonetheless, it is also important to note that it does not appear to be the case that
resilient individuals are simply unrealistically optimistic or are unaware of adverse
conditions. Rather, individuals high in trait resilience are often able to experience
positive emotions even when also fully recognizing the negative aspects of the event
or situation with which they must deal, and experiencing the negative affect (e.g.,
anxiety, frustration) associated with the event. It seems as though positive emotions
serve as a “psychological breather” (Ong et al., 2006, p. 743) in the midst of distress.
Lazarus, Kanner, and Folkman (1980) hypothesized that under stressful conditions,
when negative emotions tend to predominate, “positive emotions may provide a psy-
chological break or respite, support continued coping efforts, and replenish resources
that have been depleted by the stress” (Folkman & Moskowitz, 2000, p. 649).
These characterizations of resilience, and also our earlier considerations of the
effects of affect on cognition and mental agility, seem to treat positive and negative
emotions as largely separate, although sometimes “interspersed” affective conditions.
Yet is such separation of positive and negative emotions invariably present, across time
and circumstances within an individual, or across different individuals? Or might the
degree of independence between the positive and the negative emotions that we expe-
rience itself change in the face of adversity? And might individuals differ both in the
extent to which their positive and negative emotions appear to covary with one another,
and in how finely differentiated their responses are within those broad categories?
The ways in which the relations between positive and negative affect may dynami-
cally change, particularly during times of coping with stress, are the central focus of a
model proposed by Zautra and colleagues (2001). The model predicts that under
normal conditions positive and negative emotion are (as implied earlier) relatively
independent of one another. However, under conditions of stress, affective states may
become less differentiated from one another.
More specifically, according to the dynamic affect model, under ordinary circum-
stances it is beneficial to have distinct positive and negative emotions, or “separate
accounts” for positive and negative affect. When emotions remain distinct, they pro-
vide the individual with the maximum amount of independent information regarding
his or her affective responses because “the scope of their experience with one emotion
E motio n , S e l f, Pe rs on al it y 253
is not determined by the presence or absence of the other” (Zautra et al., 2001,
p. 787). Under these conditions, however, the amount of “uncertainty” that is present
is also greatest, because one’s knowledge concerning the type and degree of affective
experience one has with regard to a given aspect of one’s situation provides minimal
information (and so cannot reduce uncertainty) about one’s feelings with regard to
other aspects.
An implication of this is that a situation involving a high degree of affective differ-
entiation and affective complexity is likely to be more cognitively demanding—
because it involves a greater amount of uncertainty—than is a situation involving less
affective differentiation. Yet we also know that the experience of pain or high levels of
stress itself draws on cognitive resources as one attempts to cope with the stress and
the uncertainty surrounding it. According to the dynamic affect model, this competi-
tion for limited cognitive resources may lead to less differentiation of our affective
judgments during times of pain and stress. During such times, rather than little or no
relation, there may be an inverse correlation between positive and negative affective
states, with increases in negative affect accompanied by marked decreases in positive
affect. Whereas, during periods of low stress, positive and negative moods appear to
fluctuate independently, during times of high stress “positive affect becomes con-
strained by negative affect” and instead of involving independent dimensions, “the
structure of affective space approaches unidimensionality” (N. A. Hamilton, Karoly, &
Kitzman, 2004, p. 567). Nonetheless, such differentiation may also be influenced by
more stable individual differences. As will be further developed later in this section,
the differentiation between emotions may vary with differences in an individual’s
ability to understand one’s own emotions (termed “mood clarity” by Salovey & Mayer,
1990), with one’s relative emphasis on the valence (hedonic) versus arousal aspects of
emotion (Barrett, Gross, Christensen, & Benvenuto, 2001; Feldman, 1995), and with
differences in cognitive-affective complexity (Labouvie-Vief & Medler, 2002), as well
as with trait resilience.
Individuals characterized as resilient have been found to engage in several
strategies that strengthen positive emotions. Among these strategies are engaging in
positive reappraisal and “benefit finding” in the face of adversity, and using humor
(see, for example, Folkman & Moskowitz, 2004). Ongoing day-to-day monitoring of
positive emotions and stressful circumstances in older adults showed that positive
emotions could help to foster well-being both by interrupting the ongoing experience
of stress (providing a temporary respite) and by increasing the speed of adaptation to
subsequent stressors. Whereas relatively more resilient individuals could use momen-
tary interludes of positive emotion to alleviate stress, for individuals who were less
resilient, “the unpleasant experience of one daily stressful event tends to follow on the
heels of another, thereby ratcheting up subsequent stress levels even higher” (Ong
et al., 2006 p. 743). Thus, both between-person differences in psychological resilience
and within-person differences in the operation of positive emotion contribute to
whether and how flexible adaptation to adversity is observed (e.g., Bonanno, 2004,
2005; Bonanno et al., 2004).
The personality trait of “hardiness” also may help to buffer individuals against
extreme forms of stress. Hardiness involves three central components: first, a com-
mitment to finding meaningful purpose in life, involving oneself in, rather than
254 M O T I VAT I O N A N D E M O T I O N
alienating oneself from, whatever one is doing or encounters; second, the belief that
one can influence one’s surroundings and the course and outcome of events, or the
“perception of oneself as having a definite influence through the exercise of imagina-
tion, knowledge, skill, and choice” (Kobasa, Maddi, & Kahn, 1982, p. 169); and third,
the belief that one can learn and grow from both positive and negative life experi-
ences, or the “belief that change rather than stability is normal in life and that the
anticipation of changes [provides] interesting incentives to growth rather than threats
to security” (Kobasa et al., 1982, p. 170; see also Aspinwall & Taylor, 1997; Bonnano,
2004; Florian, Mikulincer, & Taubman, 1995; Kravetz, Drory, & Florian, 1993). In a
prospective study of middle- and upper-level managers over a period of 5 years, Kobasa
et al. (1982) showed that although stressful life events were associated with increases
in illness symptoms, hardiness decreased the likelihood of symptoms occurring,
particularly under circumstances involving extremely stressful life events.
Researchers have also begun to identify coping strategies that do not only mini-
mize the negative aspects of stress, but that are associated with increased positive
well-being, including feelings of energy, strength, engagement, and enjoyment (Shiota,
2006; Tugade & Fredrickson, 2004; Tugade, Fredrickson, & Barrett, 2004). Some of
these strategies overlap with those for hardiness, including positive reappraisal
(emphasizing the positive aspects to be gained from a negative event or situation),
and problem-focused coping (directing efforts toward constructively responding to
the negative event or situation). Other coping strategies that may help to increase
positive well-being include eliciting social support and creating positive events for
oneself and others (e.g., taking a few moments to appreciate natural beauty; see the
section on “Attention Restoration Theory and Experiences of the Natural Environment”
in Chapter 11). In a study of the effects of bereavement, Ong and colleagues (2006,
p. 743) found that widows characterized by high trait resilience were more likely to
“selectively mobilize positive emotions to recover and bounce back from daily stress.”
Maintaining or increasing emotional complexity—so as to preserve at least partial
separation between positive and negative emotional states and differentiating between
emotions of a similar affective valence—also may be an important aspect of resilience
(Ong et al., 2006; also see Labouvie-Vief & Medler, 2002). Whereas individuals with
high emotional granularity differentiate between related positive emotions, thus
representing positive emotional experience precisely (e.g., distinguishing between the
experience of joy vs. contentment vs. interest), individuals with low emotional granu-
larity tend to group similar emotional states together, representing emotions more
globally or generally (e.g., using all three of the former descriptors for a given state,
thereby referring to a general feeling of pleasantness). Additionally, persons with low
emotional granularity often characterize their emotions predominantly only by their
core affect, most often “valence” (Barrett et al., 2001; Feldman, 1995).
One study (Zautra et al., 2001) examined the characteristic of “mood clarity” in
individuals suffering from pain due to arthritis, or fibromyalgia involving widespread
muscular and joint pain and fatigue. Mood clarity was defined using a 10-item ques-
tionnaire measure developed by Salovey et al. (1995), on which participants indicated
their agreement versus disagreement with statements such as “I am rarely confused
about how I feel,” “I am often aware of my feelings on a matter,” and “I can’t make
sense out of my feelings” (reverse coded). It was found that, for individuals high in
E motio n , S e l f, Pe rs on al it y 255
mood clarity, changes in negative affect were not associated with changes in positive
affect. In contrast, for persons low in mood clarity, there was a strong inverse relation
between changes in negative affect and the level of positive affect experienced (Study
1). Positive affect also reduced the magnitude of the relationship between pain and
negative affect, even after accounting for the main effects of positive affect on nega-
tive affect (Study 1 and 2). In their earlier work, Salovey et al. (1995) also found that
greater mood clarity predicted recovery of positive mood following a stressful event.
Comparatively more complex representations of one’s self may exert a similar buff-
ering effect during times of stress. Linville (1985, 1987) construes greater self-com-
plexity as entailing a cognitive organization of self-knowledge or self-representation
using a greater number of cognitive self-aspects, and maintaining greater distinctions
among self-aspects. She defines a “self-aspect” as a “self-relevant cognitive category,
concept, or schema” (Linville, 1985, p. 97), with the number of self-aspects generally
increasing as an individual gains increasing experience in different roles, relation-
ships, behaviors, or situations. (Compare this account with the hierarchical model of
autobiographical memory, proposed by Martin Conway, and schematically rendered in
Fig. 2.2 in Chapter 2.) For instance, one undergraduate participant tested by Linville
(1985) provided the following trait groupings for self-characteristics: creative, alone,
with friends, real-world survival, and bad traits, placing a number of specific traits
under each of these groupings (e.g., imaginative and individualistic under “creative”).
Linville (1987) proposes that greater complexity or differentiation of the self may
help to minimize global “spillover” of negative affect associated with one domain to
other (differentiated rather than undifferentiated) aspects.
One important route may be that greater self-complexity, such as that resulting
from more extensive and varied roles and interests, could influence automatic associa-
tive processes, providing more numerous and diverse potential trains of thought and
problem solving, and also influence attention through, for instance, the activation of
different goals (e.g., Rothermund, Wentura, & Bak, 2001). Such processes might
operate at a largely subconscious level. However, it might also be noted that some
individuals in the face of high levels of stress or pain may intentionally remind them-
selves of positive benefits. The processes involved in benefit-finding in adversity might
differ from those that contribute to what Affleck and Tennen (1996) refer to as
“benefit-reminding,” involving deliberate and strategic self-reminders of the benefits,
gains, or advantages that have been obtained through the adversity (e.g., illness, pain)
that one or one’s loved one is enduring. The relative contributions of more automatic
versus more strategic processes in the emergence of the buffering effects of relatively
greater self-complexity remain to be fully determined.
It is also not known if, perhaps, individuals who are more resilient to stress and
adversity, and who also have greater self-complexity, might more often deliberately
engage in a process of thinking about what they find highly valuable and important, so
as to intentionally counteract pain or negative affect in one domain, by affirming or
reaffirming positive engagement and enduring commitments in another domain. As
will be developed in the next section, mentally stepping “upward” in one’s inner cog-
nitive-emotional world, to focus on what one most highly values, may be a surpris-
ingly potent act, with clear consequences for mental agility. Notably, findings from
two different laboratories (Schmeichel & Vohs, 2009; Wakslak & Trope, 2009) have
associated the beneficial effects arising from such inner evaluative redirection—often
termed “self-affirmation”—with a shift in one’s level of representational specificity.
Reflection on one’s values and one’s most important aspirations may induce a more
abstract level of action identification; this, in turn, may partially underpin the benefi-
cial effects on cognitive flexibility and enhanced self-regulatory capacity that have
been associated with this intervention.
first part of the study all participants were asked to consider a list of values and
characteristics such as artistic skills, creativity, relations with friends/family, and
spontaneity, and to rank order these values and characteristics in terms of their
personal importance. Thereafter, each participant was given an envelope that described
the writing assignment for the next part of the study and that comprised the
experimental manipulation (but to which the experimenter thus was blind).
In the self-affirmation condition, participants were asked to indicate their most
important value and to write an essay describing why the value was important to them
and a time when it had been especially important. In contrast, participants in the
control (no-affirmation) condition first indicated their ninth most important value
and then wrote an essay describing why this value might be important to the average
student. All participants then viewed a 12-minute educational video about AIDS that
showed six people who had contracted AIDS, each telling how they had contracted the
disease and relating their life course after learning they had the disease. Afterward,
participants were asked to rate the video with regard to several questions and to
indicate their personal risk for contracting AIDS on a 9-point scale. They were also
given the opportunity to take some educational AIDS brochures (on three different
topics) and to purchase condoms at the same price as at the student health center.
The key finding was that, after viewing the video, participants in the self-affirmed
condition perceived themselves as at greater personal risk from HIV compared
with how they had rated their perception of risk at pretest; in contrast, participants in
the nonaffirmed condition showed no significant change in their perceived risk as a
function of watching the video. Furthermore, whereas 50% of the self-affirmed
participants purchased condoms, only 25% of the nonaffirmed participants did so;
affirmed participants also were more likely to take one or more educational brochures
than were nonaffirmed participants (78% vs. 54%). These outcomes suggest that self-
affirmation both increased processing of the threatening information in the video and
heightened the intention to minimize risk in the future.
More recently, P. R. Harris, Mayle, Mabbott, and Napper (2007) examined the
responses of young cigarette smokers to graphic labels designed to warn of the haz-
ards of smoking either following a self-affirmation manipulation (requiring partici-
pants to recall as many of their desirable characteristics as they could think of) or
following a control manipulation (requiring participants to recall recent events).
Participants were shown four images that were being considered for use on cigarette
packages in the European Union, and that were designed to shock and induce strong
negative affect in smokers or potential smokers (e.g., a close-up of an open thorax
during a heart operation, with accompanying text such as “smokers die younger”).
Similar to the study on AIDS, self-affirmed participants rated these images as signifi-
cantly more personally relevant and as more threatening than did control participants;
they also reported higher intentions to quit than did the controls. In addition, the
increase in rated personal relevance was greater for those who smoked more, such that
self-affirmation moderated the personal relevance ratings and intentions of partici-
pants at high or moderate risk but did not affect the ratings or intentions of individu-
als at low risk.
A study in which young women read leaflets on the link between alcohol consump-
tion and breast cancer yielded similar outcomes (P. R. Harris & Napper, 2005).
260 M O T I VAT I O N A N D E M O T I O N
that deviated from the particular challenged identity made salient in the situation.”
More broadly:
situation involving impression formation. After this, participants were given either
self-affirming or neutral feedback.
As expected, and in line with previous findings on thought suppression, partici-
pants who had been asked to suppress the stereotype and who were given neutral
feedback showed a “rebound” of thoughts related to the suppressed stereotype—they
showed an increased likelihood of completing word fragments with stereotypic words.
Notably, however, this rebound was not observed in individuals given the thought
suppression instructions in combination with self-affirming feedback: These partici-
pants did not produce more stereotype-related word fragments than did the groups
that were never asked to suppress thoughts about the stereotype. These outcomes
imply that rebound effects may be circumvented through indirect means, “by affirm-
ing people’s positive conceptions of themselves in a domain that is completely
unrelated to the suppression task”—thereby potentially further suggesting that
“people have considerable flexibility in preventing rebound effects after thought sup-
pression” and may rely on self-affirmation resources to “effectively enhance their
capacity for mental control and reduce interference from unwanted thoughts” (Koole
& van Knippenberg, 2007, p. 675).
The results of the latter two studies raise the intriguing possibility that self-
affirmation may also prove beneficial for improving flexible thinking under conditions
where other types of unwanted thoughts repeatedly intrude on an individual’s
awareness. One such context may involve situations requiring creative or innovative
problem solving. Often, in such situations, the most easily accessed associations or
ideas do not lead to the solution but act to preclude more imaginative or novel possi-
bilities from emerging into awareness (e.g., Jansson & Smith, 1991; Marsh, Landau, &
Hicks, 1996; Marsh, Ward, & Landau, 1999; Smith, Ward, & Schumacher, 1993; see
also the discussion of “design fixation” in the first two subsections of Chapter 4). It is
an important question then, whether, given an appropriate context and framing, self-
affirmation might help to increase innovative flexibility of thinking in creatively
demanding problem-solving and problem-finding contexts that are not directly
self-relevant.2 Notably, recent findings from our lab (Wen, Butler, & Koutstaal, in prepa-
ration) have demonstrated that, compared both to a control condition involving simple
word association, and to a no-task neutral baseline control, a self-affirmation inter-
vention led to improved performance on two different problem-solving tasks: An
insight problem-solving task, and a task requiring novel on-line visual-spatial analogi-
cal reasoning and problem solving (the Cattell Culture Fair fluid intelligence test).
Participants who were presented with 12 pairs of values (e.g., thrifty and generous) and
were asked to write about personally significant experiences for one or both values in
each pair significantly outperformed participants in the word association and baseline
control conditions on a subsequent insight problem-solving task (Cohen’s d = 1.03 and
0.85, respectively) and a fluid-reasoning task (Cohen’s d = 0.65 and 0.63, respectively).
A further significant context in which the potential beneficial role of self-affirmation
in enabling suppression of unwanted thoughts might be manifested involves the
social-psychological effect known as “stereotype threat” (e.g., Aronson, Fried, & Good,
2002; Steele & Aronson, 1995). Potentially applicable to any group that may be viewed
as inferior in ability or performance in some domain, stereotype threat involves the
idea that in situations where a stereotype about a group’s abilities is relevant, the
E motio n , S e l f, Pe rs on al it y 265
1.0
European Americans - Control & affirmation
African Americans - Control
African Americans - Affirmation
0.9
Average assignment performance
(proportion of total points earned)
0.8
0.7
0.6
1 2 3 4 5 6 7 8 9 10
Performance block
Intervention
measure, Koole et al. (1999) found initial evidence to suggest that more indirectly
assessed forms of affect might mediate the effects of affirmation. They used an indirect
test of mood in which participants were very briefly shown nonsense words (e.g.,
LOWN) followed by a mask, and then were asked to indicate, from four options, which
word might have been shown. The four-word array included an affect-related word
(e.g., DOWN) and several neutral words (e.g., GOWN, TOWN). This test (with 10
positive, 10 negative, and 5 filler items) was administered, under a cover story about
subliminal perception, both before and after the affirmation manipulation. Whereas
participants in the affirmation and no affirmation conditions did not differ in implicit
affect before the manipulation, afterward those in the affirmation condition showed
an increase in positive affect with no difference in negative affect. Thus, these outcomes
268 M O T I VAT I O N A N D E M O T I O N
at least raise the possibility that, in addition to reducing the relative accessibility of
recurrent or intrusive thoughts relating, for instance, to a failure experience or stereo-
type threat, self-affirmation may help to reduce defensive processing and increase
openness to information through subtle and perhaps unconscious enhancements of
positive affect.
Notably, recent evidence suggests that an important further potential mechanism
invoked by self-affirmation involves a change in an individual’s construal level,
particularly level of specificity of action identification (discussed in the first section of
Chapter 5). In a series of experiments, Schmeichel and Vohs (2009) found that
self-affirmation helped to counteract executive resource depletion (also discussed in
Chapter 5), such that it eliminated the detrimental effect of an earlier effortful
self-control task on subsequent attempted self-control tasks. They hypothesized that
self-affirmation facilitated self-control because it helped to move the individual’s level
of mental construal to a relatively higher and more abstract level. In line with this
hypothesis, these researchers found that participants who were administered a ques-
tionnaire assessing their preferred levels of construal for various behaviors directly
after engaging in a self-affirmation exercise demonstrated higher levels of construal
than did individuals in a control condition who did not engage in self-affirmation.
Self-affirmed participants scored significantly higher on the Behavioral Identification
Form of Vallacher and Wegner (1989) than did nonaffirmed participants.
In a further experiment, Schmeichel and Vohs (2009) also found that, among
participants in a resource-depleted condition, affirming the self at a high level of action
identification, by asking participants to consider why they pursued an important value,
led to significantly greater subsequent self-control (delay of gratification) than did
affirming the self at a relatively low level of action identification, induced by asking
participants to consider how they pursued an important value. Additionally, among
participants in the resource-depleted condition, level of mental construal was signifi-
cantly predictive of subsequent delay-of-gratification performance. Other recent work
(Wakslak & Trope, 2009) has replicated and extended these findings. These investiga-
tors found that, compared with a control condition, self-affirmation led participants to
choose more abstract, higher level action identifications over lower level identifica-
tions and also to perform more accurately on a fragmented picture task requiring
global holistic processing. In contrast self-affirmation did not enhance performance on
a task that drew on more detail-oriented analytical attention, requiring participants to
identify parts that were missing from a picture (also cf. Schmeichel et al., 2011).
On the one hand, it does not seem warranted to conclude, in line with the strong
claim offered by Koole and van Knippenberg, that “an educational style that promotes
self-affirmation may inoculate individuals against the development of mental fixations
and obsessive thought patterns” (2007, p. 676). On the other hand, we have seen that
there are multiple converging sources of evidence that self-affirmation can, under some
conditions, increase flexibility of thought, and also evidence that it may help to foster
a more abstract level of construal. The consequences of self-affirmation do not appear
to be invariably beneficial, but are modified by such contextual factors as the particular
identity and goals that are salient in the situation. Nonetheless, at least under some
conditions self-affirmation may help to reduce defensiveness and to enhance receptiv-
ity to information that runs counter to or otherwise challenges an individual’s beliefs
E motio n , S e l f, Pe rs on al it y 269
different facets: Ideas, Fantasy, Aesthetics, Feelings, Actions, and Values. High scorers
on each of these facets, respectively, demonstrate open-mindedness and a willingness
to consider new ideas and to pursue intellectual interests (Ideas); both possess, and
value, a vivid imagination and fantasy life (Fantasy); highly esteem and can be moved
by art, music, poetry, and beauty (Aesthetics); are receptive to inner feelings, deeply
experience their emotions, and see them as important (Feelings); are willing to experi-
ence new activities, foods, and places, and prefer novelty to routine (Actions); and are
willing to reexamine social, political, and religious values (Values) (B. Griffin &
Hesketh, 2004).
Perhaps not surprisingly, given these characteristics, openness to experience
is the dimension of personality that has most consistently been linked to creativity
and associated aspects of creativity such as divergent thinking and increased sensitiv-
ity to perceptual, associative, and other aspects of experience. Also perhaps not
surprising, but less well known, openness to experience—perhaps due to its associa-
tion with attributes involving positive attitudes toward learning experiences, such as
curiosity—has also been found to be related to increased adaptability and proficiency
in broader contexts such as job performance. We will consider each of these aspects in
turn.
O P E N N E S S TO E X P E R I E N C E , C R E AT I V I T Y, D I V E R G E N T
THINKING, AND ORIENTING SENSITIVITY
As noted, openness to experience is the component of the five-factor model of
personality that has been most consistently linked to creativity (Carson, Peterson, &
Higgins, 2005; Dollinger, Urban, & James, 2004; L. A. King, Walker, & Broyles, 1996;
R. R. McCrae, 1987; G. F. Miller & Tal, 2007; Wolfradt & Pretz, 2001). Summarizing
evidence from a large number of studies concerning the personality characteristics
that tend to differentiate creative individuals, Feist (1998, Table 4) pointed to the two
cognitive traits “open and imaginative,” as distinguishing artists from nonartists and
“open and flexible” as distinguishing scientists from nonscientists. Commenting on
these characteristics, he explicitly and repeatedly remarked on the links between
openness and flexible thinking:
Although the causal bases of the association between openness to experience and
creativity are not known, R. R. McCrae (1987) speculated that three factors might
contribute. First, persons higher in openness to experience might simply be more
interested in and engaged by tasks that require open-ended, creative problem solving,
and so may tend to excel at such tasks. This possibility suggests that “open and
closed individuals may differ not in true divergent thinking ability but merely in test
performance” (R. R. McCrae, 1987, p. 1264). Second, individuals high in openness to
experience may, over time, have developed (or discovered) cognitive skills and strate-
gies that are associated with creative and divergent thinking, in particular flexibility
and fluidity of thought. Given that individuals higher in openness to experience
actively seek out more varied experiences and sensations, drawing on this broader
experiential “database” also then might enable more flexibility and fluency of thought.
This alternative suggests that the correlation between openness to experience and
divergent thinking should be less strong in younger than in older individuals, though,
to date, this possibility has not been supported (R. R. McCrae, 1987). Third, it may be
that individuals who have a preexisting ability to think in flexible ways actively seek
out novelty and varied experiences. That is, “individuals who easily generate new ideas,
whose cognitive processes are flexible, may develop an interest in varied experience,
just as individuals with particular competencies develop corresponding vocational
interests” (R. R. McCrae, 1987, p. 1264).
Other findings show that a broad cluster of behavioral-temperamental characteris-
tics relating to the types of stimuli that individuals are likely to notice is also corre-
lated with openness to experience. This cluster of characteristics is referred to as
“orienting sensitivity” (D. E. Evans & Rothbart, 2007, 2008; see also the discussion of
orienting sensitivity in Chapter 4, at the end of the subsection on “Perception,
Perceptual Simulation, and Hypothesis Generation”). Orienting sensitivity is con-
ceived of as a broad attentional construct that consists of three components: percep-
tual sensitivity, associative sensitivity, and affective perceptual sensitivity.
The first of these, perceptual sensitivity, relates to an individual’s awareness of
slight, low-intensity stimulation arising from either the external or internal environ-
ment. Questions such as “I often notice visual details in the environment” are designed
to tap this general aspect of attentional processing (item examples taken from the
orienting sensitivity scales of D. E. Evans & Rothbart, 2007). Associative sensitivity
refers to the frequency and remoteness of automatic cognitive activity, or spontane-
ous cognitive content that is not related to standard associations with the environ-
ment. It is measured by responses to statements such as “When I am resting with my
eyes closed, I sometimes see visual images.” Finally, affective perceptual sensitivity
relates to a person’s awareness of affect associated with low-intensity stimuli. An
example questionnaire item for this construct is, “I am often consciously aware of how
the weather seems to affect my mood.” Orienting sensitivity was most strongly related
to the intellect/openness factor (D. E. Evans & Rothbart, 2007, Table 4; Rothbart,
Ahadi, & Evans, 2000); however, consistent with relations between positive emotion
and associative processes (discussed earlier in this chapter) there was also a modestly
positive loading of orienting sensitivity on extraversion (e.g., a loading of .29 in Table 8
of D. E. Evans & Rothbart, 2007).
E motio n , S e l f, Pe rs on al it y 273
The shared variance of Extraversion and Openness […] appears to reflect the
tendency to explore or to engage voluntarily with novelty and may, in conse-
quence, be associated with plasticity or flexibility in behavior and cognition.
Extraversion classically brings to mind sociability […], but it has been more
broadly linked with positive affectivity, incentive reward sensitivity, approach
behavior and novelty/excitement seeking […]. The alternate label Surgency
[proposed by Goldberg, 1992, 1993] is intended to capture the active, explor-
atory sense of this factor more strongly. (DeYoung et al., 2002, pp. 535–536)
master knowledge and skills that are needed to overcome obstacles or problems.
Openness to experience may also be accompanied by a greater capacity for tolerance of
ambiguity (e.g., Sun, DeYoung, & Koutstaal, 2010) or for uncertainty that, as devel-
oped in the next section, and in Chapter 7, set conditions that allow for the innovative
generation of new interpretations and approaches.7 Likewise, openness to experience
may help to counteract tendencies toward confirming preestablished or prejudicial
views by encouraging greater receptivity to new or conflicting information (e.g.,
F. J. Flynn, 2005), and it may also encourage flexibility in one’s perspectives regarding
oneself and one’s possible roles in life (e.g., Whitbourne, 1986).
O P E N N E S S TO E X P E R I E N C E A N D A D A P T I V E L E A R N I N G
Considering the likely relations between the Big Five personality traits and measures
of occupational performance, Barrick and Mount (1991) predicted that whereas
conscientiousness would be a predictor of overall occupational performance, open-
ness to experience, due to its association with attributes involving positive attitudes
toward learning experiences, such as curiosity, broad mindedness, and intelligence,
would be a valid predictor of a particular aspect of occupational performance involving
training proficiency. In a large-scale meta-analysis of personnel studies across several
different occupational groups (professionals, police, managers, salespersons, skilled/
semi-skilled workers), these researchers found, as predicted, that conscientiousness
was a valid predictor of each of three aspects of occupational performance that were
considered: job proficiency, training proficiency, and personnel indices such as salary
and tenure. In contrast, openness to experience specifically predicted training profi-
ciency (e.g., training performance ratings, and productivity data; also see Salgado,
1997 for meta-analytic results showing a similar relation between training proficiency
and openness).
The findings concerning conscientiousness are consistent with similar findings
with regard to educational achievement (e.g., Chamorro-Premuzic & Furnham, 2003;
Wolfe & Johnson, 1995). The more specific correlation between openness to experi-
ence and training proficiency may relate either to attitudes toward learning or to the
ability to benefit from training, in that, unlike the other personality dimensions,
openness to experience also is moderately but consistently positively correlated with
measures of intelligence (e.g., Ashton, Lee, Vernon, & Jang, 2000; see note 5 at the
end of this volume).
The factors of conscientiousness and openness to experience have also been shown
to differentially contribute to school or academic performance (Blickle, 1996). Factor
analysis of a questionnaire that assessed the learning strategies of junior college
students yielded two factors, one that seemed to correspond to “learning discipline”
(with scales relating to aspects such as effort, meta-cognition, management of time
and learning environments, attention, and organization) and a second factor that
Blickle (1996) termed “elaboration,” which included scales relating to critical evalua-
tion, noting relationships, and searching literature. Whereas the “learning discipline”
factor was strongly correlated with conscientiousness (r = .57), the “elaboration” factor
was strongly correlated with openness to experience (r = .49). Each of the six facets of
the openness to experience factor (fantasy, aesthetics, feelings, actions, ideas, and
276 M O T I VAT I O N A N D E M O T I O N
values) was significantly positively correlated with the “elaboration” factor, but that
for Ideas (r = .59) was especially strong. A similar two-factor structure, again showing
that “elaboration” correlated with openness to experience, was obtained in a further
study with senior college students. In conceptually related work, Busato and colleagues
(1999) found that, compared with the other personality dimensions, openness to
experience was particularly strongly correlated with a meaning-directed learning style
(involving efforts to understand material precisely and critically, and to interrelate it
with other already-learned information), perhaps reflecting such characteristics as the
need for variety and cognition, and motivation.
A more direct experimental test of the relation between openness to experience
and adaptive learning is that of LePine and colleagues (2000). Although openness to
experience has not been found to be a strong predictor of overall performance in most
task contexts, LePine et al. (2000) specifically sought to evaluate whether it might
better predict performance in changing contexts. This research thus focused not only
on the learning of a task that was novel and complex, but particularly on the “unlearn-
ing” of how to perform a task in view of changed contingencies or rules, by contrasting
predictors of decision-making accuracy before a change (stable task context) versus
after an unforeseen change. As these researchers noted:
for differences in decision-making accuracy over and above the effects accounted for
by a measure of general intelligence and also beyond that accounted for by the mea-
sure of conscientiousness. Figure 6.3 shows the effects of high versus low openness to
experience on decision-making accuracy (lower values indicate greater accuracy)
during the initial phase of the experiment (prechange performance) and after the first
and second surreptitious changes in the rules.
These findings support the general claim made by these authors that “change places
demands on people that are quite distinct from demands existing during initial task
activity”—possibly because, when the environmental contingencies remain constant,
“a more automatic mode of information processing” may be used and “information
concerning correct behavior is less ambiguous” (LePine et al., 2000, p. 586).
Subsequent studies have likewise provided converging support for the specific rela-
tion between openness to experience and adaptation to occupational change or transi-
tions. In a field setting examining managerial success, Judge, Thoresen, Pucik, and
Welbourne (1999) found that managers’ ability to adaptively respond to various types
of organizational change, such as those resulting from business mergers, acquisitions,
or downsizing, was positively related to their level of openness to experience. Both
self-reports of an individual’s ability to cope with change, and independent ratings of
10
9
(lower scores reflect greater accuracy)
Decision-making performance
8
Prechange
7 performance
6 Performance after
first change
5
Performance after
4 second change
0
Low High
Openness to experience
coping with change, were positively correlated with a composite “risk tolerance”
measure comprised of measures of openness to experience, tolerance for ambiguity,
and low-risk aversion. In another study, Thoresen, Bradley, Bliese, and Thoresen
(2004) found that openness to experience predicted overall performance and perfor-
mance increases for employees engaged in a transitional phase of an organization
(a large pharmaceutical company in which employees were launching a new medica-
tion, therefore requiring them to learn new information and to seek out a new client
base) but not for those in a “maintenance” phase (that did not involve the launching
of a new product). These outcomes are consistent with the notion that transitional
phases may particularly bring to the foreground individual differences associated with
openness to experience, such as creativity, intellectual flexibility, problem solving, and
adaptability (Thoresen et al., 2004)8
Thus, curiosity may exert multiple conjoined effects that help to promote learning,
such as increasing attention, and actions undertaken in the pursuit of, or linked with,
the satisfaction of curiosity may be highly rewarding (e.g., Biederman & Vessel, 2006).
Similarly, the conceptually related construct of “need for cognition,” involving a stable
individual difference tendency to engage in, and enjoy, effortful cognitive endeavors
(Cacioppo & Petty, 1982; Cacioppo, Petty, Feinstein, & Jarvis, 1996), has been
found to be associated not only with openness to experience but also with “a general
tendency to actively invest cognitive resources independent of context” (Fleischhauer
et al., 2010, p. 90). Notably, one’s predispositional tendencies toward creative and
meaningful engagement with the world—as shown by openness to experience, need
for cognition, and also mindfulness (discussed in Chapter 3)—may itself be a modest
but independent predictor of levels of fluid reasoning ability across adults from
a variety of walks of life (Fleischhauer et al., 2010) and likewise in older adulthood
(Parisi et al., 2009). It is not only whether, or how frequently, we perform a variety
of cognitive and leisure activities that is important. Our level of thoughtful and
committed integrative engagement with those activities is likewise significant. In the
beginning of the next chapter we will continue to examine this question of how we
approach learning, but from the perspective of the beliefs that we have about the
nature of learning, and of how we respond to setbacks or failures during our attempts
to master new skills or to acquire new knowledge.
Looking Back
In this chapter, we have explored both possible short-term and longer term effects of
the experience of positive affect. We have treated such questions as the functional role
of positive emotions with respect to our goals, to our level of engagement in different
projects, and to goal prioritization, and how positive affect might influence cognitive
flexibility. Also identified were the potential long-term incremental effects of
frequently experiencing positive affect if such experiences are accompanied by an
increased tendency to explore and to embark upon varied behavioral, cognitive, and
social “essays” into different domains, succinctly characterized as the “broaden and
build” function of positive emotions. We have also turned our attention toward a
number of intersections between flexibility of mind and personality, such as the
personality trait of “openness to experience/intellect,” the pairing of this trait with
that of extraversion in a higher order personality construct involving “plasticity”
(compared with “stability”), and the effects of interventions that appear to “affirm the
self,” particularly with regard to broader, more encompassing, and more abstract
values and ideals.
Several of the emotion and personality factors that we have focused on, such as the
“granularity” with which individuals classify their emotions, and the tendency to
adopt higher level construals of one’s actions following self-affirmation interventions,
clearly involve constraints upon, or modifications of, levels of representational
specificity. This also applies to the positive correlation between openness to experi-
ence and perceptual orienting sensitivity, involving awareness of subtle differences in
one’s concrete sensory-perceptual and immediate experience. Other factors, such as
E motio n , S e l f, Pe rs on al it y 281
the tendency of individuals who are both higher in openness to experience and higher
in creativity to show attenuated “latent inhibition”—reflecting a reduced tendency to
screen from conscious awareness stimuli that have earlier proved to be inconsequen-
tial or uninformative—involve differences in levels of control (here, reduced auto-
matic or preattentive exclusion of stimuli from awareness). We also have briefly
considered the contributions of the “epistemic” emotions of interest and curiosity in
fostering agility of mind, with cross-connections not only to the “broaden-and-build”
account of positive emotions but also to our earlier explorations of the importance of
“learning to vary” (as well as to repeat) in setting the preconditions for the adaptive
generativity of behavior and thought.
7
Thoughts about Thoughts
The Control versus Noncontrol of Thinking
No matter what theories one may have, I doubt very much that
they are in one’s mind at the moment of writing a poem….
—Elizabeth Bishop (1950/2008, p. 687)
As suggested by the title, this chapter focuses on levels of cognitive control versus
noncontrol (e.g., spontaneity, automaticity) with respect to a person’s “thoughts about
thoughts,” involving higher level beliefs about cognition and oneself. We also focus on
the intersections of metacognition with more affectively and motivationally related
states such as absorption and “flow,” and intolerance of ambiguity or uncertainty.
These are considered particularly with respect to how these states may affect an
individual’s predominant level of representational specificity or level of control and, in
turn, how these can bolster, or impede, agile thinking. Each of the sections in this
chapter testifies, in different ways, to the complex “whole person” nature of mental
agility and further illustrates how thinking is neither entirely generated by nor conclu-
sively and concisely guided by that “small voice in the head” that we may associate
with explicit, deliberate, directed thinking. There is a much wider and markedly more
diverse and less docile array of contributors to our thinking. Not all of them are within
our immediate control, and not all of them are at a similar or parallel level of abstrac-
tion or level of reach to our explicit consciousness and awareness.
The eight sections in this chapter, although not exhaustive, are representative
of that range: (a) epistemological beliefs, learning to learn, and flexible thinking;
(b) jumping to conclusions and intolerance of uncertainty versus intolerance of
ambiguity; (c) optimism versus pessimism; overconfidence versus underconfidence;
(d) trying not: intentional forgetting, deliberate thought suppression, and flexible
thinking; (e) absorption, flow, and “hypoegoic” self-regulation: the controlled losing of
282
Thoug h t s abou t T h ou g h t s 283
control and the melding of thought-emotion-action; (f) working well with the uncon-
scious: incubation and complex multicomponential decision making; (g) movements
between higher and lower level goals: opportunistic design, and (h) encountering
diversity in the thoughts and views of others. As will become clear, the topics in each
of these several sections cannot be readily circumscribed to any one domain—
concepts, perception, emotion, or motivation and action—but involve complex inter-
penetrations of those domains. We begin with our beliefs about the nature of learning
and knowledge, and the related notions of how we construe “intelligence,” and how
those beliefs may, for good or for ill, recursively influence the very “subjects” or
“processes” to which they themselves refer.
A further, perhaps less obvious, but equally important, consideration concerns the
implications of an overt and explicit focus on “intelligence” as a reason for offering
praise to students or children by teachers, parents, and others. Although it may seem
beneficial to praise a child’s intelligence or ability when he or she shows high levels of
performance on a challenging task (“You must be smart at these problems!”), in a
series of studies C. M. Mueller and Dweck (1998) showed that such praise encouraged
children to focus on performance goals and implicitly promoted an interpretation of
intelligence as a fixed, internal entity. In contrast, praising a child’s efforts, or hard
work (“You must have worked hard at these problems!”), led children to focus on the
more malleable motivational aspects of intelligence. Of particular significance, praise
concerning the child’s effort rather than ability increased the likelihood that the child
later would choose challenging problems that provided opportunities to increase their
learning and skills, rather than “safe” problems that they would answer correctly.
Praise for effort rather than ability also changed what type of information children
most often requested. If given a choice between learning how others had scored on the
task, or learning about strategies that could help them to improve their own perfor-
mance, children praised for their ability more often chose to learn about how other
children had scored on the task. In contrast, children praised for their efforts were
more likely to choose to be given strategy information that could help expand their
mastery of the task. The attributions that the children made after a failure on the task
also diverged. In the face of failure, children earlier praised for their intelligence
showed lower levels of persistence and effort, more negative affect and decreases in
task enjoyment, and decreased performance compared to those earlier praised for
their efforts. These effects were found to be independent of children’s actual perfor-
mance levels. Children who received positive feedback without an explicit attribution
to either their ability or their effort (e.g., “That’s a really high score!” or “Good job!”)
showed patterns of performance and responses that were intermediate between the
ability- versus effort-attribution groups.
Stated briefly, unlike praise for appropriate task engagement, praise for intelligence
tends to encourage a focus on performance rather than learning, and on trait informa-
tion, rather than contextually variable effort, task attentiveness or involvement, and
so on. Thus, in offering praise, just as in giving criticism, it may be helpful to “separate
the deed from the doer” (C. M. Mueller & Dweck, 1998, p. 50). Nonetheless, caution is
needed in advocating overly simplistic approaches, or an absolute abstention from
trait ascriptions, regardless of circumstances. Additionally, it is important to recog-
nize that, depending on the precise phrasing that one uses, even attributions to effort
may become “trait-like” (e.g., “You’re a hard worker!”), and fostering a very strong
learning orientation might itself become detrimental if individuals too exclusively and
too exhaustively focus on mastery as an end in itself.
the situation. How does one go about gathering additional information, or deciding
what information to consider and how much, or in what order, or how to weight
varying sorts of evidence, or how to integrate sometimes apparently conflicting or
outright contradictory evidence or arguments? In such situations, personality and
emotional and motivational influences on data gathering and inference making, such
as state and trait anxiety, or one’s tolerance of uncertainty and need for cognitive
closure, emerge as important.
Individuals who have a general predisposition or tendency to respond to different
situations with high levels of anxiety, for example, show several cognitive biases
regarding information that could be perceived as signaling potential dangers or
problems (e.g., physical symptoms such as a sore throat, or aches and pains). These
biases can lead to a misinterpretation (exaggeration) of the degree of threat that is
present both externally and also internally. Persons who are high compared with low
in “trait” anxiety demonstrate increased attention to threat-relevant information
(e.g., Mathews & MacLeod, 1994), tend to interpret ambiguous stimuli as more threat-
ening (e.g., Byrne & Eysenck, 1993), and may be “on the watch” for danger, jumping to
the most threatening conclusion (Mathews & Mackintosh, 1998). They may also
be likely to overestimate the likelihood that negative events will happen to them
(e.g., G. Butler & Mathews, 1987).
A simple task designed to evaluate how personality and other factors might affect
data-gathering styles under uncertainty is the “beads task.” In this task, participants
are told that there are two jars, and that each jar has a different proportion of beads of
two colors. For example, participants may be told that one jar has 85% blue and 15%
yellow beads, and the other jar has 85% yellow and 15% blue beads. The participant
will then successively be shown beads one at a time that the experimenter draws from
one of the jars hidden from the view of the participant, and the participant’s task is to
judge from which of the two jars the experimenter is drawing. A key measure of inter-
est is the number of draws that are needed before the participant is willing to reach a
judgment concerning the jars. The task also allows examination of how participants’
judgments are influenced by the designated proportions of beads in the two jars
(e.g., when the proportions are 85:15 vs. 60:40) and by the specific order in which
beads of particular colors are drawn.
Individuals who were high compared with low in trait anxiety (as determined by a
median split of the sample) were found to request fewer beads before reaching a deci-
sion (Bensi & Giusberti, 2007) for each of three different bead ratios (85:15, 70:30,
and 60:40).2 High trait anxiety individuals also consistently tended to reach a conclu-
sion more quickly in response to other probabilistic scenarios presented via computer
(e.g., trying to decide which of two game-show contestants was the stronger player,
based on question-by-question information about whether each of the contestants
answered correctly to a series of questions).
High trait anxiety compared with low trait anxiety participants also were found to
be significantly more often incorrect in their inductions in a card selection task that
required individuals to form and test several successive hypotheses regarding which of
several cards had been covertly selected by the experimenter (Bensi & Giusberti,
2007). The task was designed so that it was not possible to conclusively rule out
each of the competing possibilities before the fifth trial of feedback was provided.
Thoug h t s abou t T h ou g h t s 287
High anxious individuals, on average, reached a decision by about the fourth trial and
were correct on only about one-third of the trials, compared with about 70% correct
responses by the low trait anxious group, who tended to wait about one card longer
before making their judgments.
Notably, however, group differences as a function of trait anxiety were not always
observed, but depended on the particular structuring of the process of data gathering
and testing. When all of the information relevant to reaching a decision was provided
together at the outset, so that there was no intervening period of uncertainty and no
further information had to be requested, then the groups who were high versus low in
trait anxiety performed similarly. These findings support the possibility that high trait
anxious individuals were likely to “jump to conclusions” under conditions in which
they were facing uncertainty and where reaching a decision more quickly would itself
terminate the uncertainty more quickly. As suggested by Bensi and Giusberti (2007),
individuals prone to anxiety may come to perceive the state of being uncertain as itself
stressful and upsetting, regardless of the objective likelihood of a positive or negative
outcome. Given that persons prone to anxiety often experience anxiety in situations
of uncertainty, they may come to have an implicit goal of uncertainty reduction, thereby
hoping to lower anxiety and discomfort, even in situations of low actual threat or
danger. Indeed, Dugas, Buhr, and Ladouceur (2004) argue that individuals who are
high in intolerance of uncertainty find uncertain situations inherently distressing—
so much so, in fact, that they may even prefer a certain but negative outcome over an
uncertain outcome.
Intolerance of uncertainty, defined as “a dispositional characteristic that arises
from a set of negative beliefs about uncertainty and its connotations and conse-
quences” (Koerner & Dugas, 2008, p. 631), also has been shown to play an important
causal and maintenance role in excessive worry, and in generalized anxiety, both in
clinical and nonclinical samples (e.g., Dugas et al., 1997; Koerner & Dugas, 2008;
Ladouceur, Gosselin, & Dugas, 2000). Intolerance of uncertainty has been measured
by a questionnaire (Freeston et al., 1994), including items relating to several different
dimensions. Among the dimensions are an individual’s behavioral attempts to control
the future and to avoid uncertainty (e.g., “I should be able to organize everything in
advance”); inhibition of action (e.g., “The smallest doubt can stop me from acting”);
emotional reactions such as frustration and stress (e.g., “The ambiguities in life stress
me”); and cognitive interpretations that imply that being uncertain reflects badly on
oneself (e.g., “Being uncertain means that a person is disorganized”). Intolerance of
uncertainty was found by Freeston et al. (1994) to predict which individuals would be
likely to meet criteria for generalized anxiety disorder, a condition in which patho-
logical worry is a hallmark symptom; importantly, the predictive value of intolerance
of uncertainty was not accounted for by shared variance with negative affect. Similarly,
Dugas et al. (2001) showed that intolerance of uncertainty in a large nonclinical
undergraduate sample explained a high proportion of the variance in the tendency to
worry, over and above that explained by related variables such as anxiety sensitivity.
Intolerance of uncertainty thus might interfere with agile thinking, both directly
and indirectly. To the degree that such intolerance leads to worry—for example, if
individuals believe that worrying increases their control over uncertain events or their
consequences—detrimental effects on problem solving would emerge if individuals
288 M O T I VAT I O N A N D E M O T I O N
interpersonal conflict? Dugas et al. (1997) suggested several steps, each of which
aims at increasing the ability of the individual to connect with the actual (concrete)
problem and his or her own experiences:
In contrast, for worries that concern highly improbable future events, these
investigators recommended cognitive exposure. Such exposure should particularly
aim at encouraging individuals to fully experience their most fearful images and the
aversive somatic/physiological activation that those images invoke—rather than the
verbal content of the worry—so as to allow them to develop a better understanding of
their own ability to tolerate emotional arousal and uncertainty.
Although intolerance of uncertainty has been found to be partially associated with
the concept of intolerance of ambiguity, and some investigations have used them inter-
changeably, they are not the same construct. (See also Excursion 6: Uncertainty versus
Equivocality.) Historically, the concept of tolerance or intolerance of ambiguity has
been associated with the way in which individuals (or groups/organizations) perceive
and process information in situations that involve unfamiliar, complex, or incongru-
ent/apparently conflicting or contradictory cues or elements (Budner, 1962; Frenkel-
Brunswik, 1948; Furnham, 1994), and it has been linked particularly to ambiguity
relating to novelty, complexity, and/or insolubility (Budner, 1962). Furnham (1994)
clearly summarized the many emotional and perceptual behavioral correlates of intol-
erance of ambiguity that were initially articulated by Frenkel-Brunswik, including:
Furnham (1994) found that the different questionnaire measures were all modestly
correlated with one another (pairwise correlations between .44 and .82). Factor analy-
ses on the questionnaires suggested several different factors. For example, one of the
scales yielded six different factors related to such aspects as problem solving
(e.g., “Nothing gets accomplished in this world unless you stick to some basic rules”),
anxiety induced by ambiguous stimuli (e.g., “I get pretty anxious when I’m in a social
situation over which I have no control”), desire to complete or finish problems (e.g.,
“If I were a scientist, I might become frustrated because my work would never be com-
pleted—science will always make new discoveries”), and adventurousness (e.g., “I like
to fool around with new ideas, even if they turn out later to be a total waste of time”);
another questionnaire yielded factors related to predictability, variety and originality,
clarity, and regularity. Thus, issues relating to uncertainty appeared to be only one
aspect of these conceptualizations of ambiguity tolerance/intolerance, which itself
appears to be a multidimensional construct involving aspects related to preferences,
anxieties, and also epistemological or philosophical preferences. Consistent with this
suggestion, based on cluster analyses of several different tasks and questionnaires,
Kreitler and colleagues (1975) concluded that ambiguity intolerance involved three
different clusters of behaviors relating to, first, intolerance of situations admitting of
multiple interpretations, second, intolerance of situations that are difficult to catego-
rize, and, third, intolerance of situations with contradictions or conflict.
There is also evidence that intolerance of uncertainty versus intolerance of ambigu-
ity may be differently related to conditions such as worry. Buhr and Dugas (2006)
empirically examined the relations between the constructs of intolerance of uncer-
tainty versus intolerance of ambiguity, and additional constructs such as perfection-
ism and sense of control, to worry in a large undergraduate sample. Although scores
on the Intolerance of Uncertainty Scale (Freeston et al., 1994) correlated significantly
and positively with scores on the Scale of Tolerance-Intolerance of Ambiguity (Budner,
1962), the correlation was only modest: r = .42. In addition, regression analyses
revealed that intolerance of uncertainty was uniquely related to worry; the relation-
ship between this measure and worry remained significant even when shared variance
associated with intolerance of ambiguity, perfectionism, and perceived control was
statistically removed.
Like intolerance of uncertainty, ambiguity intolerance may have cognitive, emo-
tional, and behavioral components. However, Grenier and colleagues (2005) suggested
that an important conceptual difference between them is that whereas ambiguity intol-
erance “refers to a static component embedded in the present,” uncertainty intolerance
has a different temporal focus on the future. Individuals who are intolerant of ambigu-
ity are “unable to tolerate a ‘here and now’ situation characterized by equivocal or
ambiguous features [. . .] these individuals interpret the present situation as a source of
threat” (Grenier et al., 2005, p. 596). In contrast, intolerance of uncertainty is orien-
tated toward the future, such that individuals high in intolerance of uncertainty “will
consider it unacceptable that a future and negative event may occur, however small the
probability of its occurrence” (Grenier et al., 2005, p. 596; see also Dugas et al., 2001).
Although, according to Krohne’s (1989) model of coping modes, ambiguity appears
to precede uncertainty, with respect to empirical evidence on the development of
anxiety and worry, it remains unclear whether intolerance of ambiguity might foster
Thoug h t s abou t T h ou g h t s 291
intolerance of uncertainty, and vice versa. In addition, the distinction between the
predominant temporal foci of intolerance of uncertainty (focused on the future)
versus intolerance of ambiguity (focused on the present) merits exploration in
relation to evidence concerning the apparent automatic processing of future event
information in clinical depression. There is evidence to suggest that depressed indi-
viduals may automatically characterize the future in negative terms (e.g., S. M. Andersen
& Limpert, 2001; S. M. Andersen et al., 1992), and also the converse of what has been
termed “automatic optimism” (Lench & Ditto, 2008) in which healthy “normal”
individuals show biased use of base rate information for positive and negative events.
Biases toward excessive pessimism or excessive optimism, in normal individuals and in
depression, are considered in the next section. Intriguingly, although both sets of
biases may arise from relatively automatic modes of processing, the precise mecha-
nisms that have been theorized to underpin these biases are quite different.
hand). However, the incentives had little effect on the predictions that the partici-
pants made. In all cases, although participants did appropriately change their predic-
tions in accord with the stated odds, they nonetheless consistently were more likely to
predict that they had winning cards than losing cards (odds ratio of 3.67, confidence
interval of 2.56–5.26). Greater optimism bias was also observed when participants
were required to respond quickly in predicting whether they would or would not
experience positive and negative future events. These findings support the notion
that, in part, optimistic bias may arise from our tendency to rely on an “affect heuris-
tic” that does not necessarily relate to extreme states of emotion, but to what Slovic
and Peters (2006) characterized as the “faint whisper of emotion,” called affect:
We use the term affect to mean the specific quality of “goodness” or “badness”
(a) experienced as a feeling state (with or without consciousness) and
(b) demarcating a positive and negative quality of a stimulus. We have used
the term “the affect heuristic” to characterize reliance on such feelings […]
the experienced feelings are used as information to guide judgment and
decision making […]. One of the main characteristics of the intuitive, expe-
riential system is its affective basis. Although analysis is certainly important
in some decision-making circumstances, reliance on affect is generally a
quicker, easier, and more efficient way to navigate in a complex, uncertain,
and sometimes dangerous world. (Slovic & Peters, 2006, p. 322)
Other findings suggest that optimism may “give way,” potentially to especially
extreme despair, under severe and sustained stressors. Hirsch and colleagues (2007)
found that, in an undergraduate sample, individuals who scored relatively high in level
of optimism continued to fend well when confronted with a number of negative life
events, including events that were potentially traumatic, suggesting that optimism
and a future-oriented perspective helped to offset stressors. However, for very large
numbers of negative life events, those high in optimism were at significantly greater
risk for experiencing ideas and imagery relating to suicide, and also for suicide
attempts, than were persons of more moderate or low optimism.
Not only have people been found to be generally overoptimistic: It appears that
they may also believe that it is best to be overly optimistic—that is, that others ought
to be optimistic (Armor et al., 2008). When asked to provide prescriptions about the
level of optimism that individuals in different realistic scenarios should display,
ranging from –4 (extremely pessimistic) through 0 (accurate) through +4 (extremely
optimistic), participants consistently prescribed a moderate level of optimism. Across
four different scenarios, including decisions about a financial investment, an academic
award application, a surgical procedure, and a dinner party, the modal prescribed level
of optimism was +2; this response was endorsed by just over 30% of the participants,
compared with only 18% who endorsed the “accurate” option. Although participants
who were asked to describe how optimistic people actually were also described people
as optimistic (mean of 0.82), participants on average recommended even greater
optimism (mean of 1.12).
The level of optimism that was recommended varied with several aspects of the
situation. Participants recommended greater optimism if the individual had already
committed himself or herself to the action (mean of 1.24) than if commitment to the
action had not yet been taken (mean of 0.61); if the decision to commit was the pro-
tagonist’s to make (mean of 1.04) than if it was not (mean of 0.80); and if the protago-
nist’s control over the outcome was high (mean of 1.34) rather than low (mean of
0.51). Intriguingly, even individuals who were themselves comparatively pessimistic,
in that they obtained trait optimism scores below the midpoint on the Life Orientation
Test-Revised (Scheier et al., 1994), also prescribed optimism for others (mean of 0.87).
These outcomes suggest that people may not always endorse a view that it is “best” or
“ideal” to be accurate in one’s predictions. Rather, they may sometimes see optimism
as both desired and desirable, and not, for example, just an unwanted or unintended
effect of motivated reasoning, or of cognitive or information-processing limitations.
Additional findings clearly point to variation in the circumstances under which
individuals tend to be optimistic versus shifting toward pessimism. Sweeny and
colleagues (2006) propose that both optimism and shifts away from optimism serve a
similar goal, namely “the need for preparedness”:
undertake challenges with the confidence that one can succeed. However, in
other circumstances, a shift from optimism best serves the goal of prepared-
ness by directing thoughts and actions toward assessing and responding to
changes in the local environment. Of course, when danger has passed or
worst-case scenarios become less dire, shifts toward optimism can also serve
the need for preparedness by directing energy toward goal attainment.
Finally, a pessimistic outlook can facilitate preparation for possible unde-
sired outcomes. As the moment of truth draws near, pessimism directs
cognitions and activity toward avoiding undesired outcomes and minimizing
their consequences. (Sweeny et al., 2006, pp. 302–303)
Adjustment of expectations downward may occur for many reasons, such as the
gathering or noticing of new information (e.g., because of greater scrutiny or anxiety,
or both) or because individuals change their level of representational specificity or con-
strual level. As events become closer in time, more concrete rather than abstract con-
struals may sharpen an individual’s focus on events that are more likely to happen
(compare with the discussion of temporal effects on construal level in the third section
of Chapter 3). In an especially illustrative study, Shepperd and colleagues (1996) found
that whereas 4 months prior to graduation college seniors were optimistic about their
salary predictions for their first position after graduation, at 2 weeks prior to gradua-
tion they were realistic. Shifts in predictions have also been found with respect to test
performance scores, with the overly optimistic predictions of performance a few weeks
before the examination decreasing immediately after the exam (to approximately the
objective level of performance), and also again slightly decreasing immediately before
feedback (to somewhat below objective levels of performance). The magnitude of the
downward shift from optimism also has been found to be greater if the outcome is
personally consequential or important compared with if it is of less importance.
In a recent brain imaging study, Sharot and colleagues (2007) found that individu-
als higher in trait optimism as measured by the Life Orientation Test-Revised (Scheier
et al., 1994) tended to more strongly expect positive events to happen closer in the
future than negative events, and they tended to experience them with a greater sense
of preexperiencing. These researchers also found that the imagination of negative
future events was associated with reduced brain activity in the amygdala and rostral
anterior cingulate cortex compared with that observed during imagination of positive
future events and all past events. These findings raise the possibility that “the optimism
bias may be related to a reduction in negative future thought,” and that “expecting
positive events, and generating compelling mental images of such events, may serve
an adaptive function by motivating behaviour in the present towards the future”
(Sharot et al., 2007, p. 104). However, as noted by Schacter and Addis (2007b), in a
commentary on these intriguing behavioral and neuroimaging findings, an important
remaining question for future work concerns how the reduction of activity in the
amygdala and anterior cingulate when thinking of future negative events might be
influenced by changes in the likelihood or imminence of a negative event. As demon-
strated by Shepperd and colleagues (1996), overoptimism may become tempered as
the “moment of truth” nears, and it will be important to examine whether both
subjective and neurophysiological indices of emotional responsiveness and vivid
296 M O T I VAT I O N A N D E M O T I O N
imagining of possible future events show changes in parallel with the temporal
modulation of overoptimism.
Mirroring the findings with respect to a general sense of optimism toward the
future, research has shown that individuals are frequently also overconfident in
particular decisions or judgments that they make (e.g., Fischhoff, Slovic, & Lichtenstein,
1977; Lichtenstein, Fischoff, & Phillips, 1982; Stankov, 1998; see Keren, 1991, 1997,
for review). Overconfidence occurs when, on average, the amount of confidence
expressed in relation to a group of decisions (as indicated as a percentage) is higher
than the accuracy of those decisions (as a percentage). In addition, individuals tend to
show modestly similar patterns of overconfidence or underconfidence across different
sorts of judgments. For example, in research in our lab, participants showed corre-
lated patterns of overconfidence in a novel paradigm that used the same stimuli to
elicit both conceptually based general-knowledge decisions (e.g., Which is larger, India
or China?) and sensory-perceptual decisions (Which physically manipulated word
appeared larger on the computer screen?). Across three experiments we found an
average across decision-task correlation of .62 for ratings of confidence, and .53 for
participants’ level of over/underconfidence (Kvidera & Koutstaal, 2008). Other
investigators have likewise reported significant positive across-task correlations using
tasks such as Raven’s Progressive matrices, vocabulary, and line-length judgment
(e.g., Stankov, 1998; Stankov & Crawford, 1996). These outcomes suggest that some
of the determinants of confidence ratings relate to relatively stable within-individual
differences that are independent of the particular decision domain.
Aspects of the particular task context may also modulate whether over- or under-
confidence is observed. For example, the magnitude of the over- or underconfidence
shown by individuals often varies with their level of decision or performance accuracy
on a task, or task difficulty. If the task is relatively difficult (individuals achieve scores
below about 65% or so), then participants tend to be more overconfident. However, if
the task is quite easy (individuals achieve scores above about 78%), then underconfi-
dence rather than overconfidence may be observed (e.g., Brenner et al., 1996). This
pattern is called the “hard-easy” effect.
Some researchers also have proposed that the processes contributing to confidence
judgments may differ for different sorts of tasks (e.g., Bjorkman, Juslin, & Winman,
1993; Runeson, Juslin, & Olsson, 2000). Specifically, tasks that are highly sensory-
perceptual in nature are thought to more frequently elicit either underconfidence or
good accuracy-confidence correspondence, whereas conceptual tasks that depend on
higher order processing more often lead to overconfidence. However, the evidence for
such a “dual-process account” is countered by other findings suggesting that confi-
dence in perceptual and conceptual decisions may reflect similar underlying processes.
For instance, using the paradigm described earlier that allowed us to use the same
stimuli to elicit both conceptual and perceptual decisions, we observed the hard-easy
effect for both sorts of decisions (Kvidera & Koutstaal, 2008; see also Andersson,
2009). In addition, after matching for levels of performance across the decision types,
we found overconfidence for perceptual decisions together with neither over- nor
underconfidence in conceptual decisions.
The magnitude of overconfidence in judgments that is observed also varies depend-
ing on the point in time at which confidence judgments are elicited, specifically whether
Thoug h t s abou t T h ou g h t s 297
confidence judgments are assessed immediately after each decision, or, instead, for a
larger number of previous decisions, such that one retrospectively estimates one’s
overall or aggregate level of performance. Whereas overconfidence is frequently
observed when individuals are asked to give their confidence ratings in their decisions
on a case-by-case or item-by-item basis, immediately after each decision, overconfi-
dence is typically less pronounced (and sometimes absent) when individuals are asked
to provide judgments regarding how well they had performed on a larger set or series
of items (e.g., Gigerenzer et al., 1991; Griffin & Tversky, 1992; May, 1986, 1987, cited
in Brenner et al., 1996).
We recently demonstrated this differential pattern of overconfidence for one or a
few, but not for many, immediately prior decisions, using a within-subject design, in
which we asked for participants’ confidence ratings after they had answered varying
numbers of two-alternative, forced-choice, general-knowledge questions (Bjornberg &
Koutstaal, in preparation). Whereas participants demonstrated significant overconfi-
dence if we asked for their confidence ratings immediately after they had answered
only one or two of the general-knowledge questions, they did not show overconfi-
dence when they were asked to make their confidence ratings for larger numbers of
prior decisions. Furthermore, overconfidence significantly linearly decreased across
the number of prior decisions (1–2, 3–4, 5–6, or 7-plus) for which confidence ratings
were required. There was also a tendency for the decrease to occur earlier for individu-
als with comparatively lower semantic short-term memory (conceptual span) scores
than for individuals with relatively higher conceptual span scores.
The latter finding is consistent with the hypothesis that one contributor to the dif-
ference in overconfidence for one or a few, versus many, prior decisions involves differ-
ent sources of evidence—and different levels of specificity—on which the two sorts of
judgments are based. Confidence ratings regarding one or a few immediately prior
decisions might be based on what Kahneman and Tversky (1977/1979) termed the
“inside view.” When decisions are made using the inside view, individuals focus on the
case at hand or the uniqueness of the current decision for coming to a conclusion. The
informational source accessed during item-by-item or “local” confidence judgments is
likely an individual’s short-term or working memory, and participants may focus pri-
marily on the specific decision they have just made. In contrast, persons taking an
“outside view” utilize distributional data when making a decision, while to a great
degree ignoring the unique details or specifics of the case at hand. This view is more
likely to be adopted when participants rate their confidence in a large number of prior
decisions (“global” confidence judgments). In this case, the informational source
accessed might include an individual’s longer term memory, such as her knowledge of
how she generally performs on similar tasks or her general sense of her level of knowl-
edge in the task domain.
The distinction between the inside versus outside views is best illustrated by an
example given by Griffin and Tversky (1992) involving an individual’s predictions
concerning one specific outcome versus the estimated frequency with which one is
likely to be correct in the long term:
A sportscaster, for example, can be asked to assess his confidence in the pre-
diction of each game as well as the number of games he expects to predict
298 M O T I VAT I O N A N D E M O T I O N
correctly. According to the present account, these judgments are not expected
to coincide because they are based on different evidence. A judgment of
confidence in a particular case, we propose, depends primarily on the balance
of arguments for and against a specific hypothesis, e.g., the relative strength
of two opposing teams. Estimated frequency of correct prediction, on the
other hand, is likely to be based on a general evaluation of the difficulty of
the task, the knowledge of the judge, or past experience with similar prob-
lems. Thus, the overconfidence observed in average judgments of confidence
need not apply to global judgments of expected accuracy. […] Evidently,
people can maintain a high degree of confidence in the validity of specific
answers even when they know that their overall hit rate is not very high.
(Griffin & Tversky, 1992, p. 431)
rather than minimizing the intrusiveness of the thoughts or images and their
unwelcome hold on our consciousness?
Intriguingly, there is strong evidence to support both the idea that intentional
thought suppression and intentional forgetting indeed may be possible, and there is
evidence to suggest that sometimes our efforts in this direction bring about the pre-
cise opposite of the hoped-for outcome. Understanding and articulating the circum-
stances under which each outcome is likely to be observed has important implications
for cognitive functioning and our ability to adaptively shape and focus our thinking.
We will first consider experimental paradigms that have provided strong evidence for
the successful deliberate exclusion of unwanted thoughts and images from thinking
and memory. Thereafter, we will turn to consider when and why such efforts may,
instead, yield paradoxical effects of increasing rather than decreasing the accessibility
of the would-be banished thoughts.
A highly informative paradigm that has been used to experimentally examine
the ability to intentionally suppress a habitual or predominant action or motor
response—rather than an internal thought—is the so-called go/no-go task. In this
task, participants typically are presented with two types of stimuli, including one set
of stimuli (e.g., the letters A, Y, L, P) to which the participant is to respond, or “go.”
These “go” stimuli usually occur quite frequently. There is also a second stimulus
(e.g., the letter X) that occurs relatively rarely to which the participant is to withhold
responding or “not go.” This paradigm has provided insights into the psychological
and neural processes that are affected in individuals with impairments in cognitive
control, such as persons with frontal lobe lesions and persons with attention-deficit/
hyperactivity disorder (e.g., A. A. Aron & Poldrack, 2005). To examine whether similar
cognitive control and suppression techniques could be applied internally to
one’s memories and thoughts, as well as to external stimuli and motor responses,
M. C. Anderson and Green (2001; cf. M. C. Anderson, 2003) modified the go/no-go
paradigm to examine go/no-go processes in thinking—thus the “think/no-think
paradigm.”
The first phase of the think/no-think paradigm is designed to initially ensure that
individuals have formed specific memories that, later, can either be accessed and
thought about, or blocked from access and suppressed. In this phase, participants are
presented with pairs of associates (cue-target pairs), such as word-word pairs or word-
picture pairs, and are asked to memorize them until they can accurately generate each
of the targets in response to the corresponding cues. Then, in the next phase, the
think/no-think manipulation is applied. In this phase, only the cues from the previ-
ously learned paired associates, and no targets, are presented. For some of the cues
the participants are instructed to try to think of and remember the target and to say
the target out loud; for other cues, they are instructed not to think of the correspond-
ing target. Specifically, they are asked to not allow the associated memory to enter
consciousness at all, even though the potent reminder cue remains clearly visible for a
number of seconds (e.g., 4 seconds). Some of the cues are presented only once and
others are presented multiple times. Importantly, not all of the previously memorized
cue-target pairs are presented in this phase: The cues for some of the previously
learned items are never presented in this second phase, thereby later providing a
“baseline” measure against which either the benefits of the “think” manipulation or
300 M O T I VAT I O N A N D E M O T I O N
this thought-suppression research with a statement that appears directly at odds with
that reached from the think/no-think paradigm. They remark:
What has compelled the interest of the scientific and clinical communities is
that suppression is not simply an ineffective tactic of mental control; it is
counterproductive, helping assure the very state of mind one had hoped to
avoid. The problem of thought suppression is aggravated by its intuitive
appeal and apparent simplicity, which help mask its false promises. (Wenzlaff
& Wegner, 2000, p. 83)
How can these conflicting outcomes with the think/no-think versus thought
suppression paradigm be understood, and what are the implications of these diver-
gent findings? Considering the think/no-think paradigm versus the typical thought
suppression paradigm, there are several differences in the situational and cognitive
task structure that may be central in accounting for the widely differing outcomes.
First, in the think/no-think paradigm, there are many discrete items, or pairs of items,
and, during the critical think/no-think phase, the experimentally provided instruc-
tions continually direct the individual to actively attempt to retrieve and think about
some of these items, and not to retrieve others. Thus the task itself requires ongoing
cognitive control and engagement, as the person responds to now this particular
presented cue and accompanying instruction (either thinking or not thinking about
the corresponding target as indicated), and then the next cue, in an ongoing, changing
but guided interaction. Second, each instance of attempted suppression of the no-
think items is relatively time limited (on the order of a few seconds) before the next
item is presented.
In contrast, the usual thought suppression paradigm involves instructions to sup-
press only one concept (e.g., Don’t think about a white bear), or one interlinked epi-
sode (e.g., Don’t think about a videotaped car accident that you just watched). The
instructions also pertain to a more prolonged period of time, usually several minutes
rather than merely seconds, and—with one exception, noted later—there are often
very few ongoing changing environmental demands beyond the instruction to try to
suppress all thoughts of the to-be-suppressed topic. The exception concerns the
instructions as to what one is to do if, despite one’s best efforts, the to-be-banished
thought nonetheless stealthily makes it way back into awareness. To measure the
degree to which individuals are able to abide by the thought suppression instructions,
there is often (though not always) a requirement to indicate in some manner (e.g., by
ringing a bell) each time that the to-be-suppressed thought nonetheless intrudes into
consciousness.3 This then sets up a paradoxical requirement: To diligently and consci-
entiously fulfill the requirement to report (and also immediately expel) each intrusion
of the thought, one needs to remember to “be alert for” any occurrences of the
thought—which will heighten its accessibility and increase the likelihood that,
eventually, the thought recurs.
Thus, the “theory of ironic processes” (e.g., Wegner, 1992) postulates that the
process of thought suppression involves two mechanisms: First, an intentional oper-
ating process that seeks thoughts and associations that will promote the desired state
(that is, thinking about anything other than the unwanted thought), and second, a
304 M O T I VAT I O N A N D E M O T I O N
more subterranean and shadowy “ironic monitoring process” that remains in the
background rather than foreground of awareness and that explicitly searches for
mental contents that might signal a failure (or imminent failure) of the intended
suppression.
However, the intricate and intimate relation between the to-be-avoided topic and
goals is not so “straightforward,” as further articulated by Navon:
Of course, with some effort, the to-be-avoided object can be kept away
from focal attention. Its mandatory activation, or its presence in peripheral
attention, however, hampers the ability to meet the goal of banning that
object from focal attention. The spread of activation […] to related concepts
Thoug h t s abou t T h ou g h t s 305
Earlier, in Chapter 2, we saw just such a self-sustaining feedback loop in the model
proposed by J. M. G. Williams and colleagues (Fig. 2.3) in explaining the links between
abstract rumination, and other factors both directly and indirectly leading to overly
general autobiographical memory retrieval and impaired problem solving in clinical
depression.
Finally, an important question concerns the neuropsychological or other individual
difference factors that may contribute to effective suppression in the think/no-think
paradigm or related paradigms, and also in real-world circumstances that might be
broadly similar to it in terms of their cognitive demands and structure. The neuroim-
aging results alluded to earlier and also other findings (e.g., M. C. Anderson, Ochsner
et al., 2004) suggest that memory suppression is supported by a network of executive
306 M O T I VAT I O N A N D E M O T I O N
refer to the so-called putting “yips,” or to the “bricks” in basketball free throw shooting
(Beilock & Carr, 2001). Substantial disruption of the skilled performance of complex
tasks may be instigated by a number of factors that increase self-conscious attention
to the task at hand—such as, paradoxically enough, supportive audiences (J. L. Butler
& Baumeister, 1998) or instructions. Wegner and colleagues (Wegner, Ansfield, &
Pilloff, 1998) found that participants who were instructed not to overshoot a golf putt
became more inclined to do just that.
Other examples include test anxiety, stuttering, depressive rumination, and some
forms of insomnia. For instance, Harvey (2003) found that instructing participants to
deliberately suppress thoughts about a particular (self-selected) topic prior to going to
sleep led participants to report that they took longer to fall asleep and experienced
more restless sleep than if participants were instructed not to try to control their
thoughts but simply to relax and let thoughts come and go. Notably, this effect was
observed not only among insomniacs but also among normally good sleepers.4 In this
and similar situations (e.g., Ansfield, Wegner, & Bowser, 1996), heightening the
amount of attention focused on controlling our thoughts and behaviors may exacer-
bate rather than alleviate the problem, undermining instead of facilitating our efforts
at self-control.
Under these and other conditions that can result in paradoxical effects of self-
control, individuals may attempt to deliberately forego efforts at deliberate conscious
control so as to respond more spontaneously, naturally, or automatically. Leary,
Adams, and Tate (2006) use the term “hypoegoic self-regulation” to designate such
cases in which people attempt to self-regulate precisely by abandoning direct efforts to
control their behavior.
One creative approach, designed to minimize an individual’s detrimental attempts
to exercise excessive control in one particular context—the game of golf—involves
what is known as “speed golf.” This is meant to deliberately change the conditions of
the game, so that thinking too much and trying too hard is not possible because of the
necessity to respond rapidly. Christopher Smith, who set a world speed-golf record,
observed, “In speed golf the subconscious takes over.” “It knows how to do every-
thing—at least in an experienced golfer it does, because it’s done it thousands of
times.” The difficulties arise when the conscious mind tries to take over too much,
particularly after an especially poor shot.
We hit bad shots because we’re human. Even Tiger Woods hits terrible shots
sometimes. But most players, instead of chalking that up to being human
and trusting the mind-body system to do it better the next time, allow the
conscious to step in and try to fix things, by telling us to take the club back
this way or move the body that way. But the moment you start thinking con-
sciously about how to do things, that destroys your ability to perform.
(Newport, 2008, Wall Street Journal, p. W4)
may seem less paradoxical if one thinks of the initial intentional act as one that sets the
conditions for later spontaneity. An analogy with some forms of prospective remember-
ing, discussed earlier (see the first section of Chapter 5), may be helpful here.
Sometimes an individual’s initial deliberate control in forming an implementation
intention sets up the conditions for the later “automatic” triggering of the desired
behavior through the form of an “if, then” conditional rule. Similarly, when the
achievement of a hypoegoic state is desired, it is possible that one takes deliberate
steps to set the later conditions for less controlled processing.
Paradoxical tactics
Increased frequency of
hypoegoic states
As posited by both action identification and construal level theory (cf. Chapter 3
and Chapter 5), more concrete mindsets can be encouraged through focusing our
attention on precisely how actions are to be performed—the immediate mechanics
and specifics of doing—rather than why the action is important, or the broad objec-
tives or implications of the action. Yet this focus also needs to be at the right level for
one’s degree of skill and expertise, and for the complexity of the task at hand. If one
becomes too explicitly involved in the steps of a highly learned, well practiced, and
now “largely automatic” complex proceduralized behavior, such as playing the piano,
this frequently interferes with, rather than improves, performance. For complex pro-
cedures that are very well learned, neither a focus that is extremely general (related to
312 M O T I VAT I O N A N D E M O T I O N
direction. Yet the success of such controlled operations will depend on the overall level
of capacity in the system, including the presence of other stressors and so on. If too
few resources are available, then the to-be-excluded thought will emerge and remain
within awareness, “capturing” thinking. It is further suggested that, in individuals
with fear of fear, a considerable amount of their attentional and control efforts are
directed inward, toward trying to control their inner emotional and physiological
state, so as to prevent the catastrophic loss of control that they fear, rather than
outward, toward understanding, mastering, and responding to the external situational
demands they are facing (e.g., delivering a public talk). The additional demands on
their attention and the efforts focused on controlling their inner state results in a
depletion of control resources that, in turn, makes the intrusion of, and capture by,
further unwanted thoughts more likely.
In persons with fear of fear, paradoxical instructions may help to reverse this
negative spiral, because now—given the explicit instructions and intentions to delib-
erately enhance and fully experience the most uncomfortable symptoms—the auto-
matic monitoring will focus on thoughts that are inconsistent with this new goal,
including thoughts that are calming or that are neutral and would enable distraction
from the discomfort. Thus, these thoughts may have an increased likelihood of enter-
ing awareness under the paradoxical instructions, so they may ultimately lead to a
more positive experience for the person. Although speculative, these and other benefi-
cial outcomes from the use of paradoxical intentions argue that the best way to “control
control” or “thoughts about thoughts” is not always direct. Sometimes we must let go
of control to gain (renewed) control. We need oscillatory range in the level of process-
ing control that we exert, not only to gain the unique benefits derived from less directly
controlled, more spontaneous or automatic cognition but also in order to gain the
most from controlled cognition itself.
The Incubation stage covers two different things, of which the first is the
negative fact that during Incubation we do not voluntarily or consciously
think of a particular problem, and the second is the positive fact that a series
of unconscious and involuntary (or foreconscious and forevoluntary) mental
events may take place during that period. (Wallas, 1926, p. 86)
problem during the intervening period significantly more often in the relaxation
condition than in the demanding intervening task condition. More recently, Sio and
Ormerod (2009) interpreted their meta-analytical finding that incubation effects for
linguistic problems were increased when the intervening tasks imposed a light cogni-
tive load, compared to either a heavy cognitive load or rest, in terms of the greater
opportunities a light cognitive load might afford for unfocused or diffuse attention
(e.g., Mendelsohn, 1976; G. Mandler, 1994; Martindale & Dailey, 1996; see also the
earlier discussion of unfocused attention in the final section of Chapter 3).
During an incubation period, low demand tasks may occupy part of the
problem solver’s attention, preventing the focused concentration that yields
strong associates. Resting during an incubation period may allow individuals
to continuously work on the problem, whereas performing high demand tasks
may shift attention entirely to that interpolated task, leading to a narrow
rather than diffused attentional focus. (Sio & Ormerod, 2009, pp. 107–108)
The relation between an intervening task and the possible beneficial effects of
forgetting or deactivation of misleading approaches or cues has also received support.
One study (S. M. Smith & Blankenship, 1989) used an ingenious method of both
increasing the likelihood of observing initial impasses in problem solving and system-
atically probing the forgetting of misleading cues. The researchers presented word-
picture puzzles to participants, with many of the puzzles accompanied by a valid and
helpful clue, but a few (critical) items accompanied by a misleading cue. The mislead-
ing cue increased the number of unsolved critical items. It was then possible to exam-
ine performance on the puzzles when they were initially unsolved and after varying
delays that were either filled or unfilled with other activities. It was also possible to
probe memory for the misleading cue.
According to the “forgetting fixation” hypothesis (S. M. Smith & Blankenship,
1989), incubation is often helpful because it enables individuals to forget problem
approaches that are incorrect, but that individuals may have become “fixated” on
during their initial problem-solving attempts. This hypothesis predicts that obtaining
the solution of a problem that was earlier accompanied with a misleading cue is most
likely to be accompanied by forgetting of the earlier misleading cue. An example
problem is “timing tim ing” for which the solution is “split second timing.” The critical
item, for which a misleading cue was provided, was “you just me” accompanied by the
clue, “besides,” whereas the correct answer was “just between you and me.” After the
participants attempted to solve each of the problems, they were unexpectedly given
the problems a second time. However, for some participants the second encounter
with the problem occurred immediately, whereas for others it occurred after a 5-minute
or 15-minute delay (either filled with a different task or unfilled).
The key findings were that participants in the delay groups showed a greater
increase in problem solving for the critical item than did participants in the immedi-
ate testing condition, and that these groups also showed a higher level of forgetting of
the misleading clue than did the control group. Several further experiments likewise
demonstrated greater improvements in solving previously unsolved problems if
participants were precluded from working continuously on the problem and instead,
316 M O T I VAT I O N A N D E M O T I O N
were asked to perform some other task in between, or simply rested, before returning
to the problems. Furthermore, these increases in solution rates for the problems were
accompanied by decreased recall of the misleading clues.
A more recent large-scale Internet-based investigation of problem solving
(Vul & Pashler, 2007) similarly concluded that interpolated time between problem-
solving attempts primarily helps individuals to reach the solutions to unsolved prob-
lems by reducing memory for incorrect problem approaches—especially incorrect
paths that are suggested via misleading clues. Indeed, this investigation found
evidence only in support of incubation as a source of forgetting of misleading
approaches, with no evidence of beneficial effects of interposed time between solution
efforts for unsolved problems if misleading clues had not been presented.
Other demonstrations of incubation similarly suggest that it may, at least in part,
be attributable to the dissipation of forms of fixation, sometimes generated spontane-
ously or naturally. For instance, tip-of-the-tongue states (TOTs; e.g., R. Brown &
McNeill, 1966; James, 1890/1981; Maril, Wagner, & Schacter, 2001) occur when
individuals are temporarily unable to retrieve knowledge (e.g., items of general
knowledge or rare words in response to a brief definition) that they subjectively feel
they do possess. In an early diary study, Reason and Lucas (1984) found that 59% of
the naturally occurring TOTs that they observed involved the intrusion of at least
one “blocking” word that was provokingly similar to the correct word, but that was
incorrect. A subsequent laboratory study suggested that such TOTs may be more likely
to be spontaneously resolved—through the individual successfully retrieving the
heretofore elusive information—after there is an interposed interval during which
the individual is presented with other unrelated questions than if probed again
immediately (H. Choi & Smith, 2005). This likewise appears to support the impor-
tance of dissipating inappropriate retrieval strategies or diminishing the accessibility
of “blocking” interlopers as contributors to incubation.
However, it could be argued that the comparatively simple types of problem-
solving tasks that Vul and Pashler (2007) investigated—namely anagrams and remote
associate problems—and similarly also TOTs, are perhaps not ideally suited to reveal-
ing the beneficial effects of less deliberate, more unconscious interposed processing
on highly complex multicomponent or ill-defined problems that may allow for
multiple solutions (cf. Penney et al., 2004). In future research, it will be important to
use similarly high-powered studies to examine whether there are benefits of inter-
posed rests between solution attempts for other, more complex types of unsolved
problems. Furthermore, although incubation-like phenomena for some problems may
predominantly reflect one mechanism (e.g., forgetting of misleading problem
approaches), other instances involving incubation-like phenomena may arise mainly
from somewhat different mechanisms.
One such mechanism involves incidental encounters with new problem-relevant
information. Whereas many laboratory tests of incubation preclude the possibility of
exposure to new problem-relevant information, incubation for “real-life” problems
may often involve the surreptitious recognition of possible solution paths to ongoing
problems that emerges when we are exposed to potentially problem-relevant informa-
tion. Real-life problems frequently involve the setting of goals for which the associ-
ated task has not yet been completed. Such “open goals” may be highly relevant to
complex forms of incubation.
Thoug h t s abou t T h ou g h t s 317
experiments have been reported that have been interpreted as evidence for the
counterintuitive conclusion that unconscious thought leads to normatively better
decision-making performance for complex problems than does conscious thought.
However, the most parsimonious and satisfactory interpretation of these findings
continues to be a matter of considerable debate.
In one series of experiments, Dijksterhuis (2004) systematically manipulated
the amount of time that participants were allowed to reflect on complex decisions,
such as choosing an apartment. Participants were presented with a description of four
hypothetical apartments, each characterized by 12 or 15 different attributes, some
positive, some negative, and were asked to form an impression of the apartments so
as to be able to choose between them at a later time. The primary manipulation
concerned what happened after the description of the hypothetical apartments. One
group of participants, the immediate decision group, was asked to make their choices
immediately, with essentially no time for either deliberate or nondeliberate thinking.
Another group of participants, the conscious deliberation group, was given 3 minutes
to deliberately evaluate the options before deciding which of the apartments was best.
Yet a third group—the key comparison group, the “unconscious” deliberation group—
was told that they needed to make a choice, but was then immediately given an atten-
tion-demanding working-memory task for an interim 3 minutes, before being asked
to directly make the choice. In contrast to the immediate decision group that was
given no deliberation time at all, and also to the second group given the opportunity
to attentively deliberate, the last group of participants was given an opportunity to
think only “without deliberate attention.”
The surprising outcome was that participants in the “unconscious” deliberation
group apparently made better choices than did either the immediate choosers or the
intentional deliberators. The unconscious deliberation group showed a greater differ-
ence in their attitudes toward the best apartment (defined as the apartment possess-
ing the most positive features and the fewest negative features) and the worst
apartment than did participants in either of the other two groups. Additionally, only
in the unconscious deliberation group was the difference in attitudes toward the best
compared with the worst apartment significantly greater than zero. Similar outcomes
were obtained in two follow-up experiments that modified the way the descriptions of
the hypothetical apartments were presented (e.g., grouped together by apartment
rather than intermixed), and that involved choosing a hypothetical roommate rather
than an apartment.
In attempting to understand these outcomes, and, more generally, the circum-
stances under which unconscious or at least minimally controlled or only intermit-
tently controlled thinking might prove superior to deliberately controlled cognitive
processing, several considerations are important. One of these is the relatively low
capacity of conscious awareness or working memory. The average capacity of working
memory is currently estimated to be approximately four items, or fewer, if unassisted
by semantic long-term memory and other forms of support.5 In some decision-mak-
ing contexts these capacity limits might lead individuals to consider only a subset of
relevant information before making decisions.
When the choices are relatively simple, involving few attributes, then deliberative
reasoning may surpass nondeliberative choice. Further work by Dijksterhuis et al.
Thoug h t s abou t T h ou g h t s 319
(2006) contrasted participants’ choices of a car, from a set of four hypothetical cars,
when each car was characterized by only 4 aspects or by 12 aspects, and again follow-
ing deliberation either with, or without, conscious attention. When the cars were each
characterized by only 4 aspects, then participants in the deliberation-with-attention
condition more often chose the most desirable car (defined as the one characterized by
the largest percentage of positive attributes). In contrast, when each of the cars was
characterized on 12 different aspects, the deliberation-with-attention group proved
significantly less likely to choose the most desirable car. Congruent with the capacity
interpretation, there also was a significant complexity by deliberation condition
interaction, such that “unconscious” deliberation yielded more optimal decisions for
the complex stimuli, whereas “conscious” deliberation had a slight (nonsignificant)
advantage for decisions regarding the simple stimuli. A similar interaction was
observed in a further study, using the same conditions, but with the difference in
attitudes toward the best and worst car as the dependent measure.
The moderating influence of stimulus complexity on the outcomes of deliberative
versus nondeliberative choice has also been demonstrated on other, more naturalistic
measures of decision satisfaction. One study (Dijksterhuis et al., 2006, Study 3) found
that correlations between the amount of thought that students reported engaging in
concerning purchased products and their degree of satisfaction with the product
differed depending on the complexity of the product. Whereas there was no correla-
tion between post-choice satisfaction and amount of thought for products of medium
complexity, r(18) = –.03, for simple products, there was a significant positive correla-
tion, r(15) = .56, p < .03, but for complex products, there was a significant negative
correlation, r(16) = –.56, p < .03.
Another important factor that may contribute to whether there are benefits of
deliberate versus less deliberate decision-making concerns the appropriate weighting
of different features or attributes of a given choice. In most decision-making contexts,
some characteristics of an object, person, or service are more important than are others,
and so should be counted more strongly than other characteristics in deciding for a
choice (if the feature is a positive characteristic) or against it (if the feature is a negative
characteristic). However, there is evidence that, under some conditions, deliberate and
conscious considerations of information may less than optimally weight information,
unduly weighting some considerations (either positively or negatively) relative to other
considerations. (See note 10 in Chapter 1, at the end of this volume, for a characteriza-
tion of heuristics as designed to reduce one or more of the effortful steps involved in
applying the “weighted additive rule” and its variants in reaching a decision.)
Seminal experiments by T. D. Wilson and Schooler (1991) showed that explicit and
analytical consideration of one’s reasons for a choice does not necessarily enhance the
quality of one’s decisions. Rather, in two quite different domains, in one case taste rat-
ings of five different strawberry jams, in the other, the selection of college courses,
these researchers found that encouraging individuals to explicitly think about the rea-
sons for their choices led to less optimal choices. In both cases, explicit encouragement
to consider the reasons for their choices resulted in a decreased correspondence between
the ratings of experts and those made by the intentionally and explicitly deliberative
choosers. For instance, the five brands of strawberry jams or preserves were selected
based on Consumer Reports magazine rankings from seven expert sensory panelists,
320 M O T I VAT I O N A N D E M O T I O N
from long-term memory. Lassiter and colleagues (2009) explain how this distinction
could account for the (apparent) advantage of the unconscious deliberation condition,
focusing on the encoding instructions given to participants:
In other recent work, Thorsteinson and Withrow (2009) provide evidence that
encouraging note-taking during the acquisition phase might modestly help to boost
choice performance, and LeRouge (2009) found evidence suggesting that distraction
before a decision may be especially beneficial to individuals who adopt a holistic or
configural processing orientation rather than a feature-based processing orientation.
More recently, Strick, Dijksterhuis, and van Baaren (2010) countered with other
evidence supporting the notion that unconscious thought effects do take place
“off-line,” not “on-line”—with the further suggestion that the extent to which benefits
of unconscious thought are observed depends on the extent to which the encoding
conditions promote thorough and organized information encoding.
Three additional remarks might be made regarding unconscious thought effects on
complex decision making. First, a recent meta-analysis of 17 experiments, including a
total of 888 participants, has suggested that, overall, there is little evidence for an
advantage to normative decision making deriving from unconscious thought, but
that, “the true effect in the population may be anything between a moderate benefit
after unconscious thought to a slight advantage following conscious thought” (Acker,
2008, p. 301; also see Waroquier et al., 2009). Second, as noted earlier, the question of
the role of unconscious thought in paradigms, such as that used by Dijksterhuis and
colleagues, can be distinguished from the question of whether time away from a previ-
ously fully attempted, but still unsolved, complex problem, might be beneficial to
problem-solving performance. As we have seen, the meta-analysis of Sio and Ormerod
(2009) showed that “incubation time” is generally indeed helpful, although, depend-
ing on circumstances, these benefits may arise through one or more of several distinct
mechanisms.
Third, Halberstadt and Catty (2008, p. 756) have suggested that a key feature
of the cognitions that are most susceptible to detrimental “reasons analysis” effects is
their experiential nature: “Subjective feelings states, including both emotional
responses and pseudo-affective reactions such as familiarity and cognitive fluency, are
not only useful decision making tools, but are also likely to be underweighted under
analytic conditions.” These investigators suggested that reasons analysis will tend to
impair judgments specifically under three conditions. Those three circumstances are:
(1) if there is a subjective cue (e.g., familiarity) that is correlated with high-quality
judgments, (2) if the decision maker normally uses the cue as a basis of his or her
judgment (regardless of whether he or she is aware of doing so, or of the predictive
validity of the cue), and (3) if the cue is underused or underweighted under analytic
conditions.
It is instructive to keep these three conditions in mind when evaluating if a given
problem-solving situation might benefit from additional emphasis on controlled pro-
cessing, or instead, from a greater stress on spontaneous or automatic forms of pro-
cessing. Also, given that, in many situations, both controlled and more spontaneous or
automatic processing may yield helpful guidance, we may want to explicitly remind
ourselves of the availability of multiple strategies. As we saw in the work of Ark and
colleagues (2006, 2007), discussed in Chapter 3, for the perceptual diagnosis task that
they examined, explicit direct instructions to use both automatic similarity-based pro-
cesses and controlled feature-based search led to more effective use of combined strat-
egies and yielded significant gains in classification accuracy.
Thoug h t s abou t T h ou g h t s 323
Lift scenario
+ + + + + ++ + + ++
Requirement
Design activities
Solution high
Solution medium
Solution low
R
15 30 45 60 75 90
Time (minutes)
Lift scenario
++ +
+ + + + +
Requirement
Design activities
Solution high
Solution medium
Solution low
R
15 30 45 60 75 90
Time (minutes)
types of activities include scenarios relating to the main problem, understanding and
elaboration of the requirements, and development of the design solution at high,
medium, or low levels of abstraction. In the figures, “light bulbs” indicate sudden
insights experienced during the task.
As noted by Guindon, both designers:
plasticity in their aims and goals as they interact with the material world, flexibly
shifting between “making” versus “finding.” In this approach, and depending on
context and other demands, aims become something that have multiple origins, in
our selves and in what the world offers.
provide reliable evidence for links between a given type of diversity and either positive
or negative diversity effects. Rather, these investigators propose that all dimensions
of diversity may “in principle elicit social categorization processes as well as informa-
tion/decision-making processes, because all dimensions of diversity in principle pro-
vide a basis for differentiation and may be associated with differences in task-relevant
information and perspectives” (Van Knippenberg & Schippers, 2007, p. 521). Similarly,
in an earlier review, K. Y. Williams and O’Reilly (1998, p. 81) emphasized the natural
tendency of individuals to use categories to simplify the world of experience, and thus
took the position that “for our purposes, the effects of diversity can result from any
attribute people use to tell themselves that another person is different.”
Adopting an alternative approach, D. A. Harrison and Klein (2007, p. 1200) have
argued that an undifferentiated notion of “diversity” itself may be a source of the con-
ceptual and empirical inconclusiveness. They suggest that “diversity is not one thing
but three things”—and that the “substance, pattern, operationalization, and likely
consequences of those three things differ markedly.” One sense of diversity is that of
separation, involving differences in position or opinion among the members of the
group on a given continuum, and reflecting disagreement or opposition. A second
sense (perhaps that often assumed in using the term diversity) is that of variety,
involving differences in the kinds or categories of information, knowledge, or experi-
ence that the group members possess. Third, diversity may also involve disparity—as
in differences in status or pay or access to valued social and other resources that the
group members may have.
D. A. Harrison and Klein (2007) propose that different theoretical perspectives,
and quite different predicted outcomes, might best fit instances of diversity in these
different cases. Informational processing accounts emphasizing the importance of
variety and selection in thinking and problem solving may most readily be applied to
“variety,” with predicted outcomes of higher levels of variety leading to “greater
creativity, innovation, higher decision quality, more task conflict, and increased unit
flexibility.” Notions of attraction based on similarity and social categorization might
more closely apply to that of separation, with predicted outcomes of “reduced
cohesiveness, more interpersonal conflict, distrust, and decreased task performance.”
The third sense of diversity, that of “disparity” might be better accounted for by yet
another theoretical perspective relating to distributive justice and equity (or injustice
and inequity), with high within-group or within-team disparity anticipated to lead to
“more within-unit competition, resentful deviance, reduced member input, and
withdrawal” (D. A. Harrison & Klein, 2007, p. 1203).
Taken together, it is clear that simple unconditional conclusions regarding the
benefits or drawbacks of diversity in team and group membership thus are not possi-
ble. The theoretical and intuitive case for the benefits of variation in perspective and
problem-solving approaches is strong (e.g., Simonton, 2003; see also the discussion
of “learning to vary” in the final section of Chapter 5), and positive effects on
performance outcomes such as decision comprehensiveness have been documented
(e.g., T. Simons, Pelled, & Smith, 1999). Nonetheless, numerous conditions may work
against the emergence of such potential benefits, leading to weak or detrimental
effects (see the references and reviews cited earlier, and also Herring, 2009; Horwitz
& Horwitz, 2007, for representative findings and further discussion).
Thoug h t s abou t T h ou g h t s 329
Looking Back
The current chapter might be seen as a hinge between the first and second parts
of the book that concentrated on concepts and categorization versus motivation
and emotion, respectively. In the initial sections of this chapter we explored the
surprisingly powerful influences of our “metacognitive” assumptions regarding the
nature of thinking, knowledge, and intelligence on how we respond to challenges and
to the experiences of failure or success—and whether and how we are likely to under-
take remedial efforts that will both overcome immediate shortcomings and also help
to build longer term competencies. Although “beliefs about beliefs” may appear to be
highly abstract and conceptual, we saw that epistemological beliefs are closely
intertwined with motivational and emotional processes. Such intertwining was also
demonstrated in the factors, such as anxiety and intolerance of uncertainty or of
ambiguity, that contribute to the quality and extent of our “data gathering” and
evidence assessment (for example, “jumping to conclusions”).
We also considered factors relating to our ability to accurately assess the outcomes
of our own behaviors, and our level of confidence in our decisions. Here, for example,
we focused on the likelihood of our accuracy in such metacognitive assessment for
immediately prior individual decisions (when much of the relevant information
contributing to the decision is likely still available within working memory, and we
may be inclined to adopt an “inside view” that focuses on the specific case at hand)
330 M O T I VAT I O N A N D E M O T I O N
I never know whether I’m going to work in color or in black and white in
advance. It’s the subject, the occasion, the place, the circumstances that lead
me to decide and I try to decide as late as possible. (Jeff Wall, 2005, np)
Thoug h t s abou t T h ou g h t s 333
Sometimes you have a very clear idea from the very beginning but very often,
and I think this is even the better situation where, the idea of the project
grows over the time and becomes more visible like a photographic paper—
where the image reveals itself over the time. (Jacques Herzog, 2005, np)
I would like that when I go back to work not to know what the end is going
to be. (Eva Hesse, 2006, p. 304)
You explore each project, and you don’t know what’s going to come out at the
end, and so it’s like an adventure. (Alison Brooks, 2005, np)
I was lucky on those islands […]; sometimes poems do not get written so
easily. Inner recesses of the mind are not at your beck and call. Perhaps there
are small elves in the head, privileged guests living there and continually busy
with their own affairs. The only connection the conscious mind has with
them is when they permit a collaboration, which perhaps neither the con-
scious nor the unconscious was capable of alone. (Al Purdy, 2000, p. 595)
Over the years, one of the hardest lessons I’ve learned is that my work
is much smarter than I am. Although I think I know what I’m working on,
the work is silently, persistently, trying to tell me what it’s truly
about—which is often more complicated and contradictory and chaotic than
I first saw or thought or intended. At this point, I often feel somewhat
uncomfortable and confused and frustrated, which I’ve also learned over
the years, probably means I’m on the right path. The key, for me at least,
is to listen deeply to what the work is trying to tell me without trying to
smooth out its paradoxes or rough edges. Often these contradictions contain
the true energy of the work, its necessary tensions, what I’d even go so far as
to call its “life.” So, by looking intently and listening long and hard to the
work—as I continue to photograph and weave in new work—eventually
the work lets me know when it’s done, or perhaps a better way of saying it:
the work lets me know when it’s done with me. (Rebecca Norris Webb,
2009, np)
… art happens. It happens when you have the craft and the vocation and are
waiting for something else, something extra, or maybe not waiting; in any
case it happens. It’s the extra rabbit coming out of the hat, the one you didn’t
put there. (Margaret Atwood, 1982, p. 347)
over time, as individuals acted, evaluated the consequences of their actions, acted
again in accord with the new information in hand, and so on.
For instance, in an extensive analysis of the planning practices of 656 firms,
researchers (Brews & Hunt, 1999) found that effective strategic planning involved
both formal planning (which might be seen as akin to the artist’s “making”) and what
is known as “incrementalism” (akin to the artist’s “finding”). Formal planning involves
a deliberate, rational and linear process in which the ends to be achieved are specified
first, and the means to attain them second. In contrast, in incrementalism, either the
ends and means are specified simultaneously, or they are intertwined. Furthermore,
the ends are seldom stated in formal documents or announced and, if they are, they
are stated in broad, general, and nonquantified terms. Means are allowed to develop
and evolve over time, in response to “learning” by the organization and individuals
within it.
Brews and Hunt (1999) argue that good planning encompasses both formal plan-
ning and incrementalism: “specific plans may represent the ‘intended’ strategy while
the inevitable incremental changes that follow as intentions become reality represent
the emergent, or ‘realized’ part of the firm’s ‘deliberate’ strategy. Both are necessary
and neither is sufficient” (p. 903). Similarly, other research suggests that, particularly
in highly dynamic complex industries, such as the computer products industry,
both strategic planning and “autonomous decisions”—made by managers in response
to changing environmental conditions without appeal to higher approval—jointly
contribute to strong financial performance (T. J. Andersen, 2000; see also Langley
et al., 1995).
Thus both at the individual level and that of groups, teams, or organizations, dis-
covering and realizing the best balance between “making” and “finding” with regard to
our aims is a delicate ever-renewed (and renewing) dance. Extremes towards either
side may lead to less than ideal outcomes. Too much emphasis on making may lead us
to insularity and rigidity, arising from our imperviousness to changing circumstances
and new opportunities; too much emphasis on finding may leave us flitting here,
there, and now there, subject to the vagaries of chance and contingencies over which
we exert too little control.
Part Three
Each of the following four chapters focuses on how the brain—through and during
our ongoing interactions with our mental, physical, and social environments—enables
and supports flexibly adaptive thinking. The current chapter and the next one
(Chapters 8 and 9) are paired or “companion” chapters that consider experimental
research, mainly from cognitive neuroscience and neuropsychology, on the neural
contributors to levels of specificity, levels of control, and their interrelations in
enabling agility of mind. The subsequent two chapters (Chapters 10 and 11) are also
paired, and they survey a wider range of evidence (longitudinal, epidemiological, and
observational as well as experimental) concerning the crucial and continual interfaces
with our broader environment that create “brain paths to agile thinking.” From the
perspective of the iCASA framework, as conceptually summarized in Figure 1.2 in
Chapter 1, together these four chapters shift our focus to the two outermost dimen-
sions—brain substrates and our wider experiential environment—within which our
mental representational landscape is always situated. We now turn to focus on how
both brain and environment contribute to both representational accessibility across
the various domains (concepts, perception, action, and emotion) and our movements
across both levels of control and levels of specificity.
337
338 BRAIN AND ENVIRONMENT
sorting on the basis of color, while ignoring the other two dimensions of shape and
number) are shown by individuals with prefrontal damage even when they can readily
state the possible categories for sorting. Despite knowing and being able to state what
the possible bases for sorting the stimuli are, the patients get “stuck” in using one
sorting rule, perseveratively continuing to respond on the basis of a categorization
rule that was previously relevant but is no longer correct.
In contrast, other findings from individuals with damage to the frontal cortex have
demonstrated a phenomenon that seems to be the opposite of such perseverative and
inflexible persistence: Such patients may also show what Duncan and colleagues
termed “goal neglect.” In goal neglect, individuals “can say exactly what it is that they
should do, yet show no apparent attempt to do it” (J. Duncan et al., 1996; J. Duncan
et al., 2008, p. 131). Although the patients can state and remember what they are to
do, it is as though those requirements just “slip from their mind” and they fail to act
in accordance with what they know.
Thus, under some conditions, it seems that prefrontal lesions make the individual
too inflexible—so that he or she does not adapt to changing circumstances and contin-
ues to adhere to rules that are no longer appropriate. Yet, under other conditions, such
individuals seem to be too readily distracted, without sustained guidance by the rules
and goals of the task. Duncan et al. (1996) summarize the multiple forms of disrup-
tion to action and decision that may emerge as a consequence of lesions to frontal
cortex, noting that deficits are frequently observed in the organization of many differ-
ent kinds of behavior:
top-down manner. Key functions of the frontal lobes are the “shaping of behavior
by activation of action requirements or goals specified at multiple levels of abstraction”
(J. Duncan et al., 1996, p. 293, emphasis added) and guiding or enabling appropriate
alternations between “active,” “controlled,” or “voluntary” modes of control, and forms
of responding that are more “passive,” “automatic,” or “stimulus-driven” (p. 263).
These basic notions of levels of specificity and levels of control are common to
many different proposals of action and self-regulation, such as the early Test-Operate-
Test-Exit model proposed by G. A. Miller, Galanter, and Pribram (1960), the self-regu-
lation model of Carver and Scheier (e.g., 1990, 2003), and the models of the
hierarchical control of particular actions described by Vallacher and Wegner’s (1987,
1989) action identification theory (considered in Chapter 3 and also in Chapter 5).
Similarly, in the “supervisory attentional system” proposed by Shallice and Burgess
(1996; R. Cooper & Shallice, 2000) there is a distinction between a “high-level” system
that is particularly called upon in situations that involve novelty or the nonroutine:
This system is “concerned with the development of strategies for tackling novel tasks
using processes of abstraction and generalisation, monitoring implementation of the
strategy, and correcting errors” (G. Cohen, 2000, p. 7). In the model proposed by
Shallice, Burgess, and colleagues, whereas the supervisory attentional system is
thought to provide top-down control mechanisms of action processing, a second
“lower” level, involving “contention scheduling” of a hierarchy of schemas, is called
upon in routine situations, allowing for more automatic activation of the needed sche-
mas for well-learned and well-practiced actions.
There are several important functional-anatomical characteristics of the prefrontal
cortex, and also several characteristics of individual neurons within prefrontal cortex,
that could enable an inherently flexibly adaptive—and abstract—representational
role. At the functional-anatomical level, the prefrontal cortex receives and sends pro-
jections to most of the cerebral cortex and also to the major subcortical systems,
including the hippocampus, amygdala, cerebellum, and the basal ganglia. The connec-
tivity and integrative capacity of this region is immense, characterized by E. K. Miller
and Buschman (2008) as a “hub of cortical processing, able to synthesize a wide range
of external and internal information and also exert control over much of the cortex.”
Furthermore, although different subdivisions of the prefrontal cortex have distinct
patterns of connectivity (for example, orbital prefrontal cortex is extensively inter-
connected with limbic regions that are particularly involved in emotion and memory,
whereas lateral prefrontal cortex is extensively connected with sensory and motor
cortex), nonetheless, there are:
At the level of single cells, recordings from prefrontal neurons in monkeys have
shown that such neurons have the ability to sustain their activity across delays of
multiple seconds, thereby providing the opportunity to encode and maintain goal-
related information across time. Munakata and O’Reilly (2003) propose that a general
principle for why the prefrontal cortex should develop more abstract representations
than posterior cortex—and thus “facilitate flexible generalization to novel environ-
ments” is because “abstraction derives from the maintenance of stable representa-
tions over time, interacting with learning mechanisms that extract commonalities
over varying inputs” (p. 10). Neurons in prefrontal cortex also can represent an
extremely wide range of types of information, from different modalities, and demon-
strate remarkable plasticity, and they can, with training, come to represent multiple—
and often abstract—rules or contingencies. Prefrontal neurons have been shown to
support same/different rule learning (Wallis, Anderson, & Miller, 2001; Wallis &
Miller, 2003; further considered in the next section) and to encode other forms of
abstract information, such as perceptual categories (Freedman, Riesenhuber, Poggio,
& Miller, 2002, also considered in the next section), numbers (e.g., Nieder, Freedman,
& Miller, 2002), the value of choice outcomes (e.g., Montague & Berns, 2002),1 behav-
ioral strategies (Genovesio et al., 2005), and intentional sets (Mansouri et al., 2006).
As we will see, the relation between levels of control and levels of specificity in
prefrontal cortex has been an intense focus of research in recent years, and several
different accounts of the structuring principles of the frontal cortex in relation to dif-
fering forms of “abstraction” have been offered. Although they differ in multiple
respects, an important divergence between the proposed accounts involves whether
they emphasize regional differences in the forms of processing operations that are per-
formed, or the type of mental representations that are present in the different regions.
On the one hand, accounts that posit processing hierarchies “require that superor-
dinate levels, operating over longer time scales, asymmetrically modulate subordinate
processing.” On the other hand, accounts that posit representational hierarchies
“require that superordinate representations form abstractions over subordinate
representations favoring generality over detail and allowing information to be
inherited asymmetrically from higher to lower levels” (Badre, 2008, p. 193). Processing
approaches take the view that cognition in prefrontal cortex “can be described in
terms of performance without specifying the representation that underlies these
‘processes’” (J. N. Wood & Grafman, 2003, p. 140). In contrast, representational
approaches—similar to the approach that has been adopted for trying to understand
the functions in posterior cortical regions, such as the representation of words, faces,
and objects in occipital and temporal cortex (considered in Chapter 9)—posit that
there are representations in prefrontal cortex that store elements of knowledge:
From the point of view of representational accounts, there is not a sharp divide
between representations and processes, insofar as the sustained activation of sets of
representations is what “processes” are. For example, the success of goal maintenance,
or its failure, involves patterns of activation in sets of representations that are either
maintained as needed, or not.
In an analytical review of different perspectives on human prefrontal cortex,
J. N. Wood and Grafman (2003) systematically evaluated several prominent theories
of frontal function and classified them as taking mainly a processing versus represen-
tational perspective, or as “hybrid” accounts encompassing both processing and
representational aspects. They grouped two theories as processing accounts: the
adaptive coding model proposed by J. Duncan (2001) and the model of attentional
control proposed by D. A. Norman and Shallice (1986) and Shallice and Burgess (e.g.,
1996). Three were hybrids of processing and representational views: the somatic
marker hypothesis of Damasio and colleagues (e.g., Bechara, Damasio, Tranel, &
Damasio, 1997), Fuster’s temporal organization account (1997, 2001), and the work-
ing memory model of Goldman-Rakic (1987, 1995). Three were grouped as represen-
tational: a connectionist model of cerebral cortical function more generally (not only
prefrontal function) proposed by Burnod (1991), E. K. Miller and Cohen’s (2001)
guided activation theory, and their own structured event complex theory (Grafman,
2002; J. N. Wood & Grafman, 2003; also see J. N. Wood & Grafman, 2003, for
additional discussion).
Several further distinctions, apart from that between processing operations versus
representations, also become relevant when one attempts to understand the relations
between levels of abstraction and control within the prefrontal cortex. One concerns
the question of what it is, more precisely, that the “abstraction” is an abstraction of.
Many forms of action control involve temporal abstraction: “the use of a single repre-
sentation to span and unite a sequence of events” (Botvinick, 2008, pp. 201–202).
Also often involved is what has been termed policy abstraction—“the use of a single
representation to cover an entire mapping from stimuli to responses” (Botvinick,
2008, p. 202), such as “turning off the light” regardless of whether that end is accom-
plished by flicking a switch, pulling a chain, or turning a dimmer knob.2 Both temporal
abstraction and policy abstraction also are related to the further notion of state
abstraction, or the “treatment of nonidentical stimuli or situations as equivalent”
(Botvinick, 2008, p. 207), as, for example, when we ignore whether words are printed
in uppercase or lowercase letters because this is not relevant to our purposes—and
thus is also related to category representations.
Another relevant distinction derives from the functional or behavioral origins
of particular associations or subgroupings of lower level with higher-level goals. It is
possible to differentiate between an instrumental structure of multicomponent behav-
iors, defined by means-ends relations, involving goals and subgoals in a part-whole
structure, versus a correlational structure, focusing on the statistical co-occurrence of
particular subunits. Using an example provided by Botvinick (2008), the action of
placing money into a safety deposit box can be decomposed into several goal and
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 1 343
subgoal portions (e.g., get the key, unlock the door, deposit money, lock the door).
However, some of these relations are common across different instrumental goals. For
example, the sequence of “get the key, unlock the door, and open the door” occurs not
only in the context of placing money in a safety deposit box but across a range of other
circumstances such as removing money from the box, checking the contents of the
safe, or securing or removing other valuables such as documents or jewelry.
Thus, particular sequences of behavior may become associated with one another
not only through their connections to a particular instrumental goal but also through
frequent co-occurrence across differing instrumental goals. Although there is a close
relationship between correlational and instrumental organization, these two forms of
organization can be differentiated from one another and may have differing effects on,
for example, the nature of the associations that we learn, and our memory for events
(e.g., Saffran & Wilson, 2003; Zacks et al., 2007). Botvinick (2008) suggests that
whereas goal-directed behavior may rely on instrumental structure, habit-based
behavior may rely on correlational structure, as when, for example, behaviors may be
triggered directly by particular environmental contexts or sequences without media-
tion of goal representations (e.g., Botvinick & Plaut, 2006; W. Wood & Neal, 2007).
Lastly, there is a strong relation between the requirements for effectively instanti-
ating action control in the right order and at the right times and working memory
capacity. O’Reilly and Frank (2006; Botvinick, 2008) enumerated three properties that
are essential to the effective control of hierarchically structured action: (1) the ability
for higher level representations to remain relatively stable in their level of activity
across varying lower level or fine-grained events, involving “robust maintenance”;
(2) the ability to rapidly and effectively select and then deselect subactions as required,
involving “rapid updating”; and (3) the ability to selectively update representations
depending on the relevant steps in the sequence of unfolding actions and their
success/failure, or “selective updating.” More generally, E. K. Miller and Cohen (2001)
propose that a key function of prefrontal cortex is “to acquire and actively maintain
patterns of activity that represent goals and the means to achieve them (‘rules’)
and the cortical pathways needed to perform the task (‘maps’—together ‘rule maps’)”
(E. K. Miller & Buschman, 2008, p. 422, emphasis in original).
We will here look at levels of control and specificity in the prefrontal cortex at
several converging levels of analysis. Based on neurophysiological recordings in the
awake behaving monkey, the crucial role of individual neurons in prefrontal cortex in
coding and maintaining a representation of rules will be demonstrated. At the systems
level, we will focus on recent functional magnetic resonance imaging (fMRI) studies
that have sought to characterize regional differences in levels of abstraction and con-
trol functions in frontal cortex in humans. We will also consider neuropsychological
and individual differences analyses, using combined behavioral, lesion and neuroim-
aging methods to map the relations between maintaining and updating goals, and
measures of fluid thinking requiring the flexible coordination and updating of multi-
ple goals and subgoals. Our consideration of the relations between updating goals,
working memory, and fluid thinking will also point to the necessity for considering
the dynamic reciprocal interactions between frontal cortex and posterior regions,
including parietal cortex and the sensory-associative cortical regions that represent
the multiple forms of information on which working memory can operate.
344 BRAIN AND ENVIRONMENT
(a) C2
C1 C3
“cats”
2-category boundary
“dogs”
D1 D3
D2
3-category boundaries
(b)
without either the head or the tail shown (mean accuracy of approximately 80%),
suggesting that the monkeys had learned to classify the stimuli not on the basis of an
individual feature but rather on the basis of a combination of features.
Many individual neurons in the lateral prefrontal cortex of the monkeys showed
activity that seemed to reflect the monkey’s decision as to whether the—sometimes
ambiguous and difficult to classify—stimulus they were seeing was a “cat,” according
to the rules, or a “dog.” That is, single neurons in prefrontal cortex coded the classifica-
tion outcome of whether the stimulus was a cat or a dog, and typically showed relatively
346 BRAIN AND ENVIRONMENT
similar patterns regardless of whether the stimulus was a “pure” instance of the
category (e.g., 100% cat) or a less pure instance (e.g., only 60% cat).
Figure 8.2 graphically presents the firing activity of two of the neurons that
showed a classification-related role. One of these neurons (shown in the upper panel)
was especially responsive to stimuli in the dog category—regardless of whether the
stimulus was 100% dog or also included an admixture of some features that were
cat-like. With regard to when it tended to be most active, this neuron showed promi-
nent activity during the delay period between the initial presentation of the sample
and also before the required choice. The second neuron (shown in the lower panel) was
especially responsive to stimuli in the cat category. This neuron showed heightened
activity in the latter portion of the sample period (when the first stimulus was still
displayed), continuing into the early portion of the delay phase. Approximately one-
quarter of some 400 randomly selected neurons were found to show such stimulus
selective effects, and of these nearly three-quarters showed main effects of category,
preferentially responding to either cats or dogs.
It is important to note that this learned categorization by individual neurons in
prefrontal cortex was not an inevitable or necessary occurrence for the animals
to learn to classify the stimuli. In principle, it might have been the case that, rather
than single neurons coding the to-be-learned categories, this information was only
(or predominantly) coded across a large set or ensemble of neurons—and it is known
that the encoding of stimuli in other areas of the brain, such as that for faces in
temporal cortex, may involve a more broadly distributed coding approach (e.g., Rolls,
2007; see also Kriegeskorte et al., 2008). However, classification at the level of the
single neuron, and classification that is not highly responsive to stimulus similarity
per se, may substantially contribute to the rapid—and ultimately highly flexible—
categorization of unfamiliar stimuli or stimuli that must be classified on the basis of
newly learned or rapidly changing contingencies.
Additional evidence in favor of such adaptively flexible categorization was provided
by efforts to train one of the monkeys who had learned the cat–dog categorization
task on a new and different three-category classification rule for the same set of stimuli
(the three-category stimulus classification is shown with the vertical bars in Fig. 8.1).
After the monkey had been trained on this new unrelated three-category classification
task, about 65% of the 103 neurons that were recorded from were found to be visually
responsive, and of these approximately 25% were stimulus selective. For example, the
neuron depicted in Figure 8.3 was differentially responsive to the new category “C”
compared with either category “A” or category “B” (upper panel), particularly increas-
ing responding to stimuli from category C toward the end of delay period and into the
early portion of the choice phase. Notably, this neuron did not differentiate between
the—now irrelevant—categories of dogs versus cats (see Fig. 8.3, lower panel). This
same pattern of “updated classification behavior” was found across all 103 neurons,
such that whereas now information about the three-category scheme was coded by all
of the neurons, there was no longer detectable information about the previously
learned, but now irrelevant, distinction between the categories of dogs versus cats.
However, not all neurons responded only to the two- or the three-category differ-
entiation: Some neurons responded to more abstract aspects of the classification tasks.
In particular, one set of neurons was observed that responded on the basis of whether
A Fixation Sample Delay Choice
13
Dog 100%
Dog 80%
Dog 60%
Fining rate (Hz) 10
4
Cat 100%
Cat 80%
Cat 60%
1
−500 0 500 1000 1500 2000
Time from sample stimulus onset (ms)
70 Cat 100%
Cat 80%
Cat 60%
60 Dog 100%
Fining rate (Hz)
Dog 80%
Dog 60%
50
40
30
20
−500 0 500 1000 1500 2000
Time from sample stimulus onset (ms)
347
A Fixation Sample Delay Choice
10
Category A
Category B
Fining rate (Hz) 8 Category C
0
−500 0 500 1000 1500 2000
Time from sample stimulus onset (ms)
0
−500 0 500 1000 1500 2000
Time from sample stimulus onset (ms)
348
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 1 349
the presented choice stimulus matched (or did not match) the sample stimulus.
Whereas approximately 9% of all of the 395 prefrontal neurons that were recorded
from in the two-classification task responded to the category of the choice stimulus
(dog vs. cat), some 11% of the neurons responded to the match/nonmatch status of the
stimulus. Some of these neurons responded predominantly to match trials, regardless
of whether it was a “dog/dog” or “cat/cat” trial, and others predominantly fired on
nonmatch trials (“dog/cat” or “cat/dog” trials). Stated differently, these neurons were
signaling information about the relation between the sample and the choice stimulus,
not about the individual identity or classification of the stimuli.
These neurons that coded the relational (match/nonmatch) status of the sample
and choice stimuli were observed in the context of a relatively concrete, albeit difficult,
visual classification task, in which the monkeys were required to differentiate between
cats (or, often, only predominantly “cat-like” stimuli) and dogs or dog-like creatures.
An important question, however, is whether such an abstract classification rule as the
match/nonmatch rule could be learned more directly by the monkeys, and whether
neurons in the prefrontal cortex would represent this abstract rule across a wider
range of stimuli, that varied across time.
In other work that aimed to address this question, Wallis, Anderson, and Miller
(2001) attempted to directly train two monkeys to flexibly switch between using the
matching rule versus nonmatching rule on a trial-by-trial basis. The trial was a match
trial if the stimulus shown on the sample and the test display was exactly the same
(identity match), whereas a mismatch trial occurred if the sample and test display dif-
fered. The experimenters provided cues as to whether the rule for the upcoming trial
was to respond on the basis of a match or, instead, on the basis of a mismatch, between
the two stimuli. The rule that was to be used on each trial was signaled to the monkeys
by one of two cues (e.g., for Monkey A, either a drop of juice or a blue background
indicated that the match rule should be used, whereas no juice or a green background
indicated that the nonmatch rule should be used; for Monkey B, a high vs. low audi-
tory tone and juice vs. no juice cues indicated the match vs. nonmatch rules, respec-
tively). The rule instruction cue for each trial was briefly presented (for 100 ms)
concurrently with the sample stimulus.
In addition, four different objects were used on each day of training and testing.
Changing the objects every day required the monkeys to learn the rules separately
from (abstracted from) the particular stimuli that they were shown. Furthermore, the
use of four different objects on each day made it impossible for the animal to accurately
predict the upcoming stimulus that would follow the presentation of the sample stimu-
lus (nonmatches could be any one of the three other stimuli that were operative that
day), and also necessitated that the animal remember both the current sample stimu-
lus and the current rule (matching rule or nonmatching rule) in order to perform well.
Activity was recorded from a total of 492 neurons, located in the dorsolateral,
ventrolateral, and orbitofrontal prefrontal cortex. Nearly 40% of the neurons showed
activity that reflected the currently operative rule (match/nonmatch) for the trial,
showing very similar levels of activity regardless of the specific sample that was
presented. Furthermore, a subset of 69 neurons showed an especially high level of
abstraction, responding only on the basis of whether the rule indicated for a given trial
was match or nonmatch, without regard to the modality of the instructional cue (e.g.,
a visual cue vs. a gustatory/taste cue), thus suggesting supramodal coding of the rules.
350 BRAIN AND ENVIRONMENT
These findings were replicated and extended in another study (Wallis & Miller,
2003), in which the monkeys were asked to apply the match/nonmatch rules to
stimuli that differed on every trial. The observation of similar findings under these
varying conditions further supports the notion that the monkeys had learned general,
abstract rules, and that their successful application of the rules was not constrained
to the sensory details of either the stimuli or the instruction cues that were used to
indicate which rule was currently in place. Thus, the animals could flexibly, adaptively,
and highly efficiently apply the match/nonmatch rule to novel cases. The researchers
concluded:
In line with these and other findings, Duncan (2001) proposed an “adaptive coding
model” of prefrontal cortex, central to which is the idea that:
Building on this notion, Duncan (2001) argued that adaptive coding implies both
selective attention or a selective emphasis on currently relevant inputs and a deem-
phasis on nonrelevant inputs, and further implies that adaptive coding assumes a key
role in the control of processing:
Nonetheless, there was one unexpected outcome from the follow-up study of Wallis
and Miller (2003) and also of a further study from this group (Muhammad, Wallis, &
Miller, 2006). This unanticipated outcome concerned the predominant location of the
neurons that responded earliest to the match/mismatch rules. Based on the findings
of the effects of prefrontal cortical lesions on categorization performance in human
patients, it was anticipated that, in the monkeys, the neurons that coded the match/
mismatch rule would predominantly be found in prefrontal cortex rather than in the
more posterior region of frontal cortex comprising the premotor cortex. However, this
was not the pattern that was observed in either study. In both studies (Muhammad,
Wallis, & Miller, 2006; Wallis & Miller, 2003), although there certainly were neurons
in prefrontal cortex that coded the match/mismatch rules, there were relatively
stronger match/mismatch rule effects in premotor cortex than in prefrontal regions.
Given the abstract nature of the represented rule, this outcome also is apparently
contrary to many recent neuroimaging findings with humans—to be considered in
the following section—that strongly suggest that comparatively abstract rules are
represented in relatively anterior regions of the prefrontal cortex, whereas specific
rules (e.g., concrete stimulus-response associations) are represented in the more
posterior regions of frontal cortex, including premotor cortex.
The likely explanation for this outcome is important, and it very clearly shows the
necessity of considering not only the level of specificity of the representations involved
(abstract vs. specific) but also the level of practice or experience that has been acquired
with respect to the relevant task (level of control). In these studies, the monkeys were
highly familiar with the rules and had performed the tasks for many months. In con-
trast, the difficulties that animals show (Dias, Robbins, & Roberts, 1997) and that
people with prefrontal lesions show in adaptively learning and using abstract rules or
categorizations are most clearly observed for tasks which are novel and are not highly
practiced or familiar (Shallice, 1982; Shallice & Burgess, 1996; however, see also Allain
et al., 1999; Zanini, 2008).
Additionally, there is neuroimaging and neurophysiological evidence that the
relative importance of prefrontal cortex in sustaining task performance may change as
a function of increasing practice on a task. For example, neurons in prefrontal cortex
respond more vigorously when an animal is initially learning a novel and reversing cue
association in which it must first learn to associate a given stimulus with a response
(e.g., to look toward the right in response to instruction cue A) but then, later, to do
the reverse (e.g., to now look toward the left in response to cue A), than when it is
responding on the basis of an already-learned, nonreversing cue-response association
that the animal has known for days or weeks (Asaad, Rainer, & Miller, 1998).
In humans, positron emission tomography (PET) and fMRI studies have shown
that prolonged performance of tasks such as repeatedly generating verbs in response
to nouns may lead to decreases in brain activation in the prefrontal cortex as the task
352 BRAIN AND ENVIRONMENT
becomes increasingly familiar and “automatic,” and the responses increasingly stereo-
typed and habitual (e.g., Buckner, Koutstaal et al., 2000; Raichle et al., 1994). Changes
in the relative amount of activity in prefrontal cortex, with a comparative increase in
premotor cortex activity (dorsal premotor cortex, BA8B) for well-learned compared
with novel task rules, also have been shown (Boettiger & D’Esposito, 2005). Thus, it
may be the case that, as suggested by Wallis and Miller (2003, p. 1804), prefrontal
cortex “plays a greater role in rule acquisition but then, with increasing practice, the
task becomes more strongly encoded in ‘downstream’ motor system structures.” This
interpretation is, then, consistent with the multilevel perception-action hierarchy that
has been proposed by Fuster (e.g., 2004, 2006, 2009; see also Chapter 1 and Fig. 1.5),
in which although prefrontal cortex is “at the apex” of the hierarchy, nonetheless, for
relatively simple or for highly familiar, well-learned behaviors, sensory-to-motor trans-
formations can occur at relatively lower levels, including the premotor cortex.
slightly more advanced level, but still involving stimulus control, participants were
shown squares that were green, red, or white, and they needed to make a left button
key-press response for green squares, a right button response for red squares, and to
ignore white (distractor) squares.
In contrast, at the second level, involving contextual control, selection of an appro-
priate stimulus-response association depended on an external contextual signal. For
example, here participants were shown letters in one of two different colors (white or
green). If the letter was green, then participants were to respond by deciding whether
the letter was a vowel or a consonant.
In the third condition, involving temporal or episodic control, control depended on the
temporal episode in which the stimuli occurred; this condition required the monitoring
of ongoing events and ongoing internal goals. For example, here participants were
shown letters in one of three colors (yellow, blue, or cyan), and the color of the letters
signaled which tasks they were to perform: cyan signaled that they were to ignore the
letters, yellow indicated that they were to perform the consonant/vowel judgment
task, and blue indicated that they were to perform an uppercase/lowercase judgment.
These researchers predicted that the three levels of control—episodic, contextual,
and sensory control—would make cumulative contributions to cognitive control, such
that brain activity during tasks requiring these levels of control would gradually sum
354 BRAIN AND ENVIRONMENT
up from anterior lateral prefrontal cortical regions to more posterior and premotor
frontal regions. Consistent with this broad framework, using motor and cognitive
tasks designed to tap these three levels (including those described earlier, and con-
ceptual replication conditions of each), Koechlin et al. (2003) found that the
most posterior region of frontal cortex, that is, premotor cortex, was activated
for all three manipulations. In contrast, lateral prefrontal cortex/anterior premotor
cortex was activated for the sensory and context levels, and the most anterior
region of anterior lateral prefrontal cortex was activated for the episodic level only.
These three regions of frontal cortex are schematically shown in the lower panel of
Figure 8.6.
The theoretical account proposed by Koechlin et al. (2003) focuses on levels of
control (rather than representation). In contrast, according to the account proposed
by Badre and D’Esposito (2007), the anterior to posterior axis of the prefrontal cortex
“comprises a representational hierarchy, in that the character of processing at all levels
of the hierarchy is the same (i.e., computationally uniform)” (p. 2083); more specifi-
cally, “the functional gradient along the anterior-to-posterior axis of the PFC derives
from a representational hierarchy ranked by the abstractness of the representation to
be selected, rather than by the control signal” (p. 2084).3
In an extensive and analytically powerful fMRI experiment involving four “mini-
experiments,” Badre and D’Esposito (2007) used a classing rule to define four levels of
competition between the representations to be selected, from more concrete to increas-
ingly abstract. These four levels, further characterized later, involved competition
among (1) manual responses (e.g., the motor aspects of a key-press response), (2) sets
of perceptual feature-to-response mappings, (3) perceptual dimensions that comprise
a set of relevant perceptual features, and (4) sets of contextual cue-to-dimension map-
pings. They predicted that, as the competing representations became more abstract,
activation would systematically progress along the anterior-to-posterior axis, starting
from the premotor cortex (for manual responses) up to the most anterior regions of the
prefrontal cortex (for the contextual cue-to-dimension mappings).
Importantly, in addition to the manipulation of these four levels of representa-
tional competition, there was a further parametric manipulation of the degree of control
(that is, how much control) that was needed to achieve accurate performance. The
number of possible competing responses was parametrically varied from a single
potential response (one relevant response, involving no competition), to an intermedi-
ate amount of competition (two possible responses), to a high level of competition
(four possible responses). This allowed analysis of the amount of competition present
within each level of abstraction. Thus, whereas the hierarchical level of control was
assessed by the locus of the activation along the anterior-to-posterior axis, the amount
of competition between responses was assessed by the level of activation within a given
locus (i.e., point along the axis). Stated differently, as the number of possible competing
responses increases, there should be an increasing need for control to “decide” or
“adjudicate” among the alternatives, leading to increased activation. However, accord-
ing to the proposed account, the location of this activity will differ depending on the
level of abstraction involved. For tasks involving purely manual responses, activity
should be located in premotor cortex, whereas for tasks requiring contextual cue-to-
dimension mappings activity should be found in anterior prefrontal cortex.
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 1 355
For the most concrete level of the hierarchy, involving manual responses, during
fMRI scanning, participants were shown colored squares one at a time, and all four
colors mapped to one response (no competition), or two colors mapped to one response
whereas two other colors mapped to another response (some competition), or each of
four colors mapped to a different response (maximum competition). The task demands
in this experiment were quite concrete (nonabstract) inasmuch as there was only one
cue dimension that was relevant throughout (color) and the cue features (individual
colors) were always relevant to the response that was to be given. Thus, there was very
little competition at higher levels of the hierarchy concerning the task (e.g., partici-
pants did not need to consider which dimension was relevant, or whether the dimen-
sion was relevant in one context but not in another).
For the second level of the hierarchy, correct responses were conditionalized on the
presence of a second feature. As in the manual response level, participants were shown
colored squares one at time and were required to make responses to each stimulus.
However, now each colored square also contained a difficult-to-name object, and the
rules mapping to the responses depended on a further dimension of the objects (either
texture or orientation, in a between subjects manipulation) that could take one of four
values. For example, for the orientation dimension, the feature could be up, down,
left, or right. On each trial, one particular feature (e.g., “up”) was relevant. If the
relevant feature was presented, then participants were to make a positive response,
pressing a particular key. If, however, the relevant feature was not presented, then
participants were to make a negative response. In addition, the cuing as to which
feature was relevant depended on the color of the square that surrounded the object.
Therefore, in order to determine how to respond, the participant needed to consider
both the color of the square and the particular feature of the object, considering these
two factors in conjunction in order to make a response. As in the response experi-
ment, four color-to-feature mappings were relevant to each block of trials, but now
rather than the colors mapping directly to the correct responses, they now mapped to
relevant object (orientation or texture) features that then cued the correct response.
Also, as in the response experiment, the amount of competition was systematically
manipulated by varying the number of feature-to-response sets that were relevant:
one, two, or four feature-to-response sets were relevant.
In the experiment just described, the required correct responses were conditional
on the particular conjunction of color and feature (orientation or texture) that was
present; however, these dimensions (either color and orientation, or color and
texture) were always relevant, and no additional higher order constraints or rules
needed to be taken into account. This differed in the next level of the hierarchy, in
which participants were again shown colored squares one at a time. Now, however,
each square contained two objects, and participants were required to compare the two
objects along one of four possible dimensions—texture, orientation, shape, or size—
and to indicate with a key-press whether the two objects matched or did not match
along this particular dimension. The color of the square surrounding the objects cued
participants as to which dimension was relevant for that trial. In some blocks only one
dimension was potentially relevant, in other blocks two dimensions, and in others all
four dimensions were potentially relevant. The color-to-dimension mapping remained
the same across all conditions.
356 BRAIN AND ENVIRONMENT
These results provide strong empirical support for the hypothesis that cogni-
tive control is organized in a representational hierarchy along the rostro-
caudal [anterior-posterior] axis of the frontal lobes. Furthermore, these
results suggest that levels of the representational hierarchy, and so subre-
gions of the PFC [prefrontal cortex], may be differentiated by the level of
abstraction at which the representations that guide action must be selected
over competition. Abstraction is defined based on a classing rule whereby
more abstract representations generalize across a class or set of representa-
tions at subordinate levels. (Badre & D’Esposito, 2007, p. 2094)
Abstract plan/schema
/internal monitoring Branching
control
(b) (d)
RRRRRRRR RRRRRRRR
Concrete features
(F1 and F2) Response conflict
F F F F F FF F
Dimension conflict
Second-order relationships C C
(F1 = F1) ~= (F1~= F2) Context conflict
To directly contrast the outcomes of the experiments by Koechlin et al. (2003) and
those of Badre and D’Esposito (2007), Badre (2008) superimposed graphic depictions
of the peak locations of brain activation on an inflated brain surface in a common
coordinate space (Talairach space). These peak locations are shown in Figure 8.6b.
In the figure, activations are shown as 8 mm spheres (this level of smoothing or spatial
averaging was within the spatial smoothing kernel used in each of the experiments).
Also shown in this composite rendition are the different levels of abstraction of the
experimental manipulations from first-order abstraction (closest to motor cortex) to
fourth-order abstraction (anterior prefrontal cortex).
The remarkable convergence of the two studies is clear. The actual extent of the
activations, from the whole-brain analyses of the Badre and D’Esposito (2007) study
are shown in Figure 8.6a. Shown at the right of Figure 8.6 are the activation time
courses (percent signal change in the fMRI BOLD response), in the three regions
corresponding to the first-order (response), second-order (feature), and third-order
(dimension) manipulations in the 2007 study. The three time courses within each
region correspond to the parametric manipulation of the level of response conflict or
competition within the task (low, medium, high conflict). As can be seen, in each of
the three regions, activation was greatest when response competition within the task
was greatest. The final bar graph, at the lower right, presents the average percent
358 BRAIN AND ENVIRONMENT
(a)
(i) (ii) PMd
% Signal change
0.4
0.2
PMd −0.2
1 2 3 4 5 6 7 8 9 10 11 12
TR (sec)
prePMd
prePMd 0.2
% Signal change
0.1
IFS
FPC 0
−0.1
1 2 3 4 5 6 7 8 9 10 11 12
IFS TR (sec)
0.6
% Signal change
0.4
0.2
(b) 0
1st order
2nd order abstraction −0.2
1 2 3 4 5 6 7 8 9 10 11 12
abstraction a b TR (sec)
3rd order
FPC
abstraction
Mean epoch % SC
0.1
4th order c
abstraction
f
e d
0
g
Episodic
control Low Medium High
Contextual
control Conflict: High
Badre and Desposito Medium
(2007)
Koechlin et al. (2003)
Low
signal change in the most anterior prefrontal region of the brain, for the fourth-order
(context) manipulation, averaged across each of the epochs or sessions in which the
three levels of conflict (low, medium, high) were present.
These findings very clearly demonstrate the intersection of representational levels
of specificity and levels of control at multiple levels of specificity and multiple levels of
control (low to high response conflict) in frontal cortex. Whereas the predominant
location of the frontal brain activity evoked by a given task changed depending on the
level of abstraction that was needed to encode and apply the task rules appropriately,
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 1 359
the level of activation in a given region depended on the extent to which applying the
rule (at whatever level of abstraction) occurred in the face of many competing alterna-
tives, with greater (higher amplitude) activation in the face of many than in the face of
few competing possibilities. Notably, although in the studies we have considered, the
evidence for an anterior-to-posterior gradient in the representation of increasingly
abstract rules involved explicit experimenter-provided instructions concerning the
rules, a similar pattern has been observed when participants were asked to learn
task rules at differing levels of abstractness through feedback, rather than explicit
instructions (Badre, Kayser, & D’Esposito, 2010). Participants were given trial-by-
trial feedback to learn a task that had only first-order policy rules (i.e., only one-to-one
mappings) and a task that was, in addition, governed by a second-order policy rule
(i.e., there was also a rule about the one-to-one mappings that could be inferred or
learned). Whereas the task with only a first-order policy rule recruited a more
posterior frontal region (dorsal premotor cortex), the task with a “rule about rules”
additionally recruited a more anterior region (pre-premotor cortex). Examination of
participants’ performance across the task further indicated that early activation in the
pre-premotor cortex, but not in the dorsal premotor cortex, was positively correlated
with the acquisition of the second-order rule and that activity in pre-premotor cortex
for the first-order only rules task may have decreased when the higher-level search for
rules yielded no such rules.
We next turn to consider the neural correlates in humans of switching between
rules in response to external cues (during set shifting, reversal learning, and task
switching), and of the spontaneous (rather than reactive) changes in our task sets that
often enable agility of mind. Here, findings from neuropsychology, and also neuro-
chemical investigations especially focusing on the role of the neurotransmitters
serotonin and dopamine, will prove especially informative.
multidimensional stimuli)” (Swainson et al., 2000, p. 597). Often tests of set shifting
involve following a new rule that is the opposite of a previously followed rule, such
that “attend to A, ignore B” becomes “attend to B, ignore A.” Set shifting in this sense
is a central aspect of the Wisconsin Card Sorting Task (see, for example, the first
section of Chapter 2, with regard to AJ’s high level of perseverative errors on this task)
and other sorting tasks (e.g., the color/shape game conducted with preschoolers,
discussed in the fourth section of Chapter 1). It also is a key component of several
other tasks, such as the intradimensional/extradimensional attentional set-shifting
task from the Cambridge Neuropsychological Test Automated Battery (CANTAB). This
task requires the test-taker to shift responding within a stimulus dimension (e.g.,
from one color to another color) versus between stimulus dimensions (e.g., from color
to shape) as a function of changing patterns of reinforcement (e.g., Purcell et al., 1997;
Robbins et al., 1998).
Reversal learning at a conceptual level seems broadly similar to set shifting. However,
rather than involving a reversal of the individual or organism’s attentional set, rever-
sal learning involves a reversal of stimulus-reinforcement associations, such that the
learned reinforcement contingency “choose A, not B,” must become “choose B, not A.”
Reversal learning has been characterized as a form of “affective shifting” in which the
person or organism must update associations between stimulus and reinforcement to
accord with changing contingencies (e.g., Fellows & Farah, 2003, 2005).
Set shifting may occur within an already relevant stimulus dimension, called an
intradimensional shift (e.g., from yellow to red, in the case of color, or vice versa), or
between stimulus dimensions, including to a previously irrelevant dimension, an
extradimensional shift (e.g., from yellow to circles, involving a shift between the stim-
ulus dimensions of color vs. shape). An important difference between extradimen-
sional set shifting and reversal learning is that whereas reversal learning involves only
a change in exemplar, not in category, extradimensional set shifting requires a change
in category: “The extra-dimensional shift is representative of higher-order processing
because it requires taking a fundamentally new approach to solving a task that entails
a new strategy” (Ragozzino, 2007, p. 356).
Patients with prefrontal lesions may show selective disruptions of shifts that are
extradimensional but not intradimensional (Owen et al, 1991; 1993), suggesting that
they may have difficulties in rejecting higher order but not lower order rules (Wise
et al., 1996). Compared with healthy young adults, healthy older adults may also show
impairments in extradimensional but not intradimensional set shifting (Owen et al.,
1991).
Reversal learning appears to depend on the integrity of ventromedial regions of
the prefrontal cortex. Using a simple computerized card game with “play money”
stakes, Fellows and Farah (2003) compared the performance of individuals with
predominantly dorsolateral versus ventromedial prefrontal lesions to that of controls.
Participants were dealt two cards at a time from packs of different colors and were
asked to choose one of the two cards. One of the packs consistently yielded a win of
$50, whereas the other consistently yielded a loss of $50, and feedback was given after
each trial. If participants correctly chose the winning pack for eight consecutive trials,
then the payoff reinforcement contingencies were switched; this procedure occurred
for a total of 50 trials, allowing for up to five reversals of the payoff relation.
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 1 361
Whereas the patients with frontal lesions and the controls did not differ in the aver-
age number of errors that they made on the first associative learning block, the groups
clearly diverged after the reversal of the rewards, with patients with ventromedial pre-
frontal lesions making significantly more errors. In addition, the extent (volume) of
lesion damage in ventromedial regions was positively correlated with the number of
reversal errors, but errors did not correlate with lesion volume overall (total lesion
volume). Across groups, there also was a significant negative correlation between the
frequency of reversal errors on this task and the day-to-day functional abilities of the
patients, suggesting that impairments in the ability to learn new evaluative or affec-
tive contingencies might be related to flexible adaptability in everyday behavior.
A subsequent study (Fellows & Farah, 2005) extended these findings, using two
versions of a gambling task. One of these versions required reversal learning and was
similar to what has become known as the Iowa Gambling Task, in which decks that are
initially highly rewarding are in the long-term highly punitive. The second version,
however, did not require reversal learning. It was a shuffled version of the Iowa
Gambling Task, in which participants experienced the losses associated with each deck
in the first few choices, thereby preventing the formation of an initial preference for
the deck that was, in the long-term, more risky and costly. The results showed that the
degree of impairment on the simple reversal-learning task was significantly positively
correlated with improved performance on the “less beguiling” shuffled variant of the
gambling task. Thus, those individuals who had performed most poorly on the simple
reversal task benefited the most from being presented the version of the gambling
task that did not require them to “unlearn” the proclivity to choose the deck that,
though initially highly rewarding, was most disadvantageous in the longer term.
Lesions to ventromedial cortex also may influence other forms of decision process-
ing, beyond those involved in reversal learning. For example, in an ingenious study in
which participants were asked to choose one apartment from a number of alternatives,
Fellows (2006) found clear evidence for a different approach to information gathering
in the ventromedial lesion group compared with either controls or individuals with
dorsolateral frontal lesions. Using a computerized interface to present a “decision board,”
participants were asked to successively query for information about the apartment
options. They could ask for information either by comparing the different apartments
on the basis of a given attribute (e.g., noise level) or by considering several attributes for
each apartment individually (e.g., various aspects of Apartment A). Whereas both con-
trols and patients with lesions to dorsolateral frontal cortex predominantly requested
information on an attribute basis (e.g., comparing several apartments on the attribute
of their size), the ventromedial lesion patients mainly requested information for
a given alternative, that is, one apartment at a time, rather than across attributes.
The latter decision strategy of considering one alternative at a time may reflect a
tendency toward “satisficing” (seeking an acceptable or “good enough” alternative that
meets the minimal requirements necessary to achieve a goal) rather than “maximiz-
ing” (seeking the best alternative). The tendency to engage in maximizing in normal
individuals has been associated with the desire to avoid regret—leading people to con-
tinue to search even after a satisfactory alternative has been identified, so as to
decrease the likelihood of later regret should they have failed to identify and consider
a more appealing alternative (B. Schwartz et al., 2002).
362 BRAIN AND ENVIRONMENT
Notably, the different groups did not differ in the total amount of information they
requested, before reaching a choice, or in the amount of time that they spent before
their choice. Given the complex nature of the alternatives, there was no single “right”
or “wrong” answer. However, the “modal” choices for the ventromedial lesion group
did differ from the modal choices for the other two groups, and significantly differed
for multidimensional choices involving four apartments and six attributes per apart-
ment. In addition, although the overall total amount of information considered did
not differ between the groups, there was a large amount of variability in the amount
of information considered. Whereas for the simplest choices (involving two apart-
ments, characterized on four attributes) the other groups considered almost all of the
information available this was not true for nearly half of the ventromedial patients.
Indeed, nearly one-third of the ventromedial patients only examined information
about one of the alternatives before choosing it. Although additional research is
needed to determine the reasons for the different pattern of choices in the individuals
with ventromedial lesions, these findings converge with other evidence that damage
to ventromedial cortex is associated with impairments in the ability to evaluate
options (e.g., Bechara et al., 1997; 2005) and with impairments in “flexibly represent-
ing the context-specific value of stimuli more generally” (Fellows, 2006, p. 950).
Deficits in reversal learning—a task that requires the flexible updating of stimulus-
reinforcement associations—are one clear instance of such impairments in flexible
context-specific representation.
At the neurochemical level, the neurotransmitters serotonin and dopamine are
strongly implicated in enabling flexible and context-appropriate cognitive control.
First considering serotonin, dysregulation in serotonergic function has been found to
contribute to several disorders in which cognitive inflexibility is often a prominent
characteristic, including depression, schizophrenia, and obsessive-compulsive disor-
der (OCD). For example, patients with OCD have been found to show response time
(but not accuracy) deficits in reversal learning and these deficits positively correlated
with the severity of OCD (Valerius et al., 2008). Acute depletion of tryptophan—
which is an essential amino acid precursor to serotonin—in humans may impair
performance on visual discrimination reversal tasks, on which orbitofrontal cortical
lesions also disrupt performance (Fellows & Farah, 2003).
Acute tryptophan depletion also has been found to adversely affect performance on
a probabilistic task of reversal learning (Evers et al., 2005). In this modified version of
the reversal-learning task, participants were asked to choose between the same two
abstract patterns on each trial, trying to infer the current rule on the basis of feedback
given after each trial. However, the feedback was also occasionally misleading so that
correct responses were sometimes responded to as though they were incorrect, and the
participant had to infer the current rule in the face of such probabilistic feedback.4
Growing evidence suggests that serotonin is particularly involved in modulating the
processing of aversive signals, consistent with its implicated role in anxiety and mood
disorders, such as OCD and depression, that involve heightened sensitivity to threat-
related stimuli, punishment, or negative feedback. In healthy volunteers, dietary deple-
tion of tryptophan has been found to decrease the effects of positively valenced words,
for example, slowing responding to words such as “joyful” and “success” (F. C. Murphy
et al., 2002). Daw and colleagues (2002) proposed that whereas rapid phasic modulation
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 1 363
loop in Parkinson’s disease patients more vulnerable to possible “overdosing” than the
dorsolateral loop.
Similar differential effects on behavioral performance also have been reported in
healthy normal individuals, with pharmacologically increased availability of dopamine
(through administration of the D2 dopamine receptor agonist bromocriptine) leading
to improvements on a spatial working memory span task, but impairing certain aspects
of reversal learning (Mehta et al., 2001). These impairments in reversal learning were
particularly prominent when the task was novel, perhaps because dopamine turnover is
already increased in novel situations (Feenstra et al., 1995). Mehta and colleagues
concluded that regions of the cortex thought to be critical for reversal learning—
including the ventromedial/orbital prefrontal cortex (e.g., Dias et al., 1996) and the
inferotemporal cortex (Swainson et al., 2000)—“are also ‘overdosed’ in normal volun-
teers when the situation and tasks are novel to them” (Mehta et al., 2001, p. 19).
Likewise, in a review of a variety of drugs that can enhance cognition, de Jongh and
colleagues (2008) similarly noted the potentially facilitatory—or detrimental—effects
of dopaminergic promoting substances, including bromocriptine, d-amphetamine, and
pergolide, on cognitive function. Although each of these dopaminergic agonists has
been found to improve cognition in healthy volunteers, particularly working memory
and executive function, a number of studies have also indicated that the beneficial
effects may be restricted to individuals with a low baseline working-memory capacity,
whereas high-span individuals may show no improvement, or even get worse.
These studies thus provide convergent support for an earlier proposal, forwarded
by G. V. Williams and Goldman-Rakic (1995), that the relation between levels of
dopamine in prefrontal cortex and working memory performance may follow an
“inverted U” function: neither too much, nor too little, is ideal. These researchers
developed an innovative approach in which they combined single-cell recordings in
the monkey with the focal application of D1 antagonists to neurons in prefrontal
cortex that appeared to act as “memory fields” during a working memory task. These
“memory field” neurons have been found to increase firing when the monkeys must
retain the location of a target during a delay period between the presentation of the
target and the response. In addition, different neurons have been shown to encode
different target locations, and, notably, failures of the neurons to maintain their
activity during the delay period are robustly associated with errors on the behavioral
task—suggesting that these neurons provide the cellular basis for working memory.
When applying selective D1 receptor antagonists on to these neurons, G. V. Williams
and Goldman-Rakic (1995) found that, below a certain dosage level, the antagonists
enhanced the delay period activity of the cells whereas high dosage levels essentially
abolished activity in those neurons. These enhancement effects were highly specific to
the precise target position information that the neuron encoded and also included
selective facilitation of inhibitory processing in two inhibitory memory cells.
G. V. Williams and Goldman-Rakic (1995) concluded that these findings provided
“evidence of a unique dopaminergic modulation” that can be “extraordinarily precise,
affecting a specific component of the neuron’s afferent (excitatory and inhibitory)
input without affecting its general excitability.” More broadly, they concluded that
these outcomes argue that “there is an optimal level of D1 receptor occupancy for
the generation of memory fields.” Under task conditions that require a high level of
366 BRAIN AND ENVIRONMENT
motivation, cortical dopamine levels may already be elevated toward the high end of
the normal range. If so, then blocking a portion of D1 receptors may prevent their
supraoptimal (excessive) activation. Collectively, these findings “emphasize how finely
tuned is the dopaminergic regulation of cortical processing, and may help to explain
the vulnerability of these processes to dopamine dysfunction in conditions of stress,
ageing, drug use and disease” (G. V. Williams & Goldman-Rakic, 1995, p. 575). Perhaps
also, given the acute sensitivity of dopaminergic regulation to the combination of
task, motivational, and physiological factors, it may be less surprising to us that a
diverse range of conditions can exert marked effects on tasks that place high demands
on an individual’s cognitive flexibility.
Intriguingly, a third neuromodulatory input to the prefrontal cortex and basal
ganglia—that of noradrenaline (also called norepinephrine)—likewise plays a key role
in cognitive flexibility. For example, Kehagia et al. (2010, p. 202) recently proposed
that “task switching may exhibit distinct neurochemical profiles depending on the
abstraction of the rule that governs a task set, similarly to those during attentional
set-shifting.” Whereas switching between simple stimulus-response mappings
“governed by lower order rules” may rely on dopamine, similarly to reversal learning
and intradimensional set shifting, switching between higher order rules “pertaining
to categories of stimuli” may have a noradrenergic substrate, similarly to extradimen-
sional set shifting. The role of norephinephrine, particularly in relation to adaptive
responding to novelty, will be considered in a later part of Chapter 9.
TA S K S W I TC H I N G
Although set shifting and reversal learning provide highly informative and useful
measures of cognitive flexibility, in order to obtain a more direct measure of flexible
intentional cognitive control, many researchers have adopted task-switching para-
digms (e.g., Monsell, 2003). In these paradigms, participants typically are asked to
perform one of two different tasks, in response to instructional cues that either cue
them to switch from the current task to the second, not currently performed, task
(“switch” trials), or to continue (“stay”) with the task they are currently performing.
This basic paradigm can allow examination of a surprisingly large number of questions
relating to the relative “costs” to response time or accuracy that ensue from the neces-
sity to switch tasks, and a systematic characterization of when, how, and if individuals
are able to prepare, in advance, for an upcoming change in tasks (often referred to as
“task set reconfiguration”).
In general, findings have shown that performance is slower and less accurate on
trials that require a switch than on trials where the same task is repeated from an
earlier trial (e.g., Allport & Wylie, 2000; R. D. Rogers & Monsell, 1995). Nonetheless,
the magnitude of the “switch costs” that are observed can be altered by a large number
of factors, such as the amount of time between the instructional cue to switch tasks
and the presentation of the stimulus requiring a response, and whether the stimulus
that is presented has previously or recently been associated with the “old” (potentially
interfering) task or the “new” (currently relevant) task.
There is growing evidence that responses to a particular stimulus may be modu-
lated by multiple aspects of the “history” of one’s experiences with that stimulus
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 1 367
(see also the discussion of theoretical perspectives on automaticity in Chapter 1). For
example, a stimulus may elicit an inappropriate “task set” or a stimulus may be responded
to more slowly if the current decision regarding the stimulus (e.g., “yes” to a given
semantic classification task) differs from that made on a previous occasion (e.g., “no” to
the same semantic classification question or a slightly different question; e.g., Race,
Badre, & Wagner, 2010). Although this sort of stimulus-to-decision binding (Dobbins
et al., 2004) was initially proposed to be highly specific to a particular stimulus (Schnyer
et al., 2007), other evidence suggests that such rapid binding of a stimulus with a deci-
sion, perhaps into an “event file” (Hommel, 1998, 2004) or “integrated stimulus-response
episode” (Waszak, Hommel, & Allport, 2003), can generalize to other semantically or
categorically related items, facilitating subsequent processing if the decision is the same
across the tasks, but leading to no facilitation or even detracting from performance if
the decision differs (Denkinger & Koutstaal, 2009; Waszak et al., 2004).
These and related findings (e.g., Horner & Henson, 2009) suggest that largely
automatic associative linkages between cognitive events may arise at multiple levels
of abstraction, not only with respect to the particular stimuli that we encounter
(e.g., different exemplars of an object, such as different benches, or different umbrel-
las) but also at the level of the decisions we make, such that an affirmative response
“yes” to one question in regards to a stimulus subsequently might automatically
influence our speed and accuracy of responding to another (even quite unrelated)
question concerning that same or a similar stimulus that likewise requires either an
affirmative “yes” or a negative “no” response. That is, learning including automatic
learning or associative binding is continuously occurring at multiple levels of abstrac-
tion and at multiple levels of our ways of interacting with the world, including not
only stimulus processing but also our decisions and the particular ways in which we
express our decisions via concrete motor responses in the world (e.g., by pressing one
key, rather than another key). Such continuous learning, at multiple levels of an
experienced event (stimulus, cognitive decision, motor response) and at multiple
levels of abstraction, may then influence the ease with which, and the accuracy with
which, we will be able to “switch” between different tasks, with differing or partially
overlapping task requirements and stimuli (see also Coane & Balota, 2010, for discus-
sion and application to our experiential encounters with words in differing contexts).
Automatic associative learning is thus one factor that clearly may influence task
switching. Here, however, we will focus on two quite different examples of compara-
tively transient or immediate term influences on task switching performance. We first
consider the effects of momentary inductions of positive affect, which also has been
linked with alterations in dopaminergic levels, on task-switching indices of cognitive
flexibility. Next, we will consider a recent study that sought to examine the behavioral
and neural correlates of spontaneous, rather than experimentally manipulated,
moment-to-moment changes in cognitive flexibility and to assess how such changes
might impact the ease with which participants responded to instructional cues to
either maintain the current task or to switch to a new task.
The frequently beneficial effects of mild positive affect on tasks tapping cognitive
flexibility, such as verbal fluency, categorization, and various forms of problem solving
were considered in Chapter 6. According to a neuropsychological theory of positive
affect that has been developed by Ashby, Isen, and colleagues (1999), the cognitive
368 BRAIN AND ENVIRONMENT
and behavioral effects of positive affect are mediated by changes in dopamine func-
tion. For example, these researchers propose that positive affect influences creative
problem solving, in part, through increased dopamine release in the prefrontal cortex
and anterior cingulate cortex that then improves cognitive flexibility through enhanc-
ing the ability to overcome dominant responses. Nonetheless, not all studies have
found that the inducement of positive affect leads to behavioral benefits, and some
studies have reported the opposite pattern, with positive mood impairing perfor-
mance on tasks such as the Stroop color-word task, in which participants must switch
between reading color words and naming the color of the ink in which the words are
printed (Phillips et al., 2002; see R. L. C. Mitchell & Phillips, 2007, for integrative
review and discussion, and for additional evidence that, perhaps due to the “inverted
U” function relating dopamine to optimal functioning, mild positive mood may impair
not only switching but also updating and planning).
To examine the relation between positive mood and cognitive control more
analytically, Dreisbach and Goschke (2004; see also Dreisbach et al., 2005; Dreisbach,
2006) developed a task that would permit separate assessments of the effects of posi-
tive mood on the maintenance versus switching of cognitive sets. They hypothesized
that whereas positive affect would bolster the ability to switch between cognitive sets,
if needed, and thus reduce perseverative behavior, at the same time this increased
flexibility would be accompanied by an increase in distractibility, such that the
attention of individuals in a positive mood might be more likely to be “captured” by
irrelevant (to-be-ignored) novel stimuli. The participants’ momentary mood was
manipulated by the presentation of emotional pictures that were positive, neutral, or
(in a follow-up experiment) negative. Notably, the presentation of the pictures was
relatively brief, and directly preceded each of the task trials.
The task involved several phases. First, participants were presented a series of
stimuli (pairs of letters or pairs of digits) on the computer screen, with instructions to
respond to target stimuli that appeared in one color (e.g., black letters) while ignoring
distracter stimuli that simultaneously appeared in the other color (e.g., white letters).
Then participants were assigned to one of two switched task conditions, with all par-
ticipants tested in each condition. In one of the conditions, the participants were
asked to respond to stimuli in a new color while ignoring distracters that appeared in
the previous target color. In this condition, the researchers hypothesized that the
increased cognitive flexibility arising from a positive mood should facilitate the disen-
gagement from the previous task rules by inducing a bias toward novel stimuli, thereby
leading to a decrease in switch costs. In contrast, in a second condition, for the new
task that the participants were asked to perform, the targets were presented in the
previously to-be-ignored color, whereas the distracters appeared in the new color.
Here, increased cognitive flexibility should again bias attention toward novelty but
now that bias would have the effect of making the task more difficult—because the
novel stimuli are in this condition irrelevant to the new task.
The results strongly supported their predictions. In the condition that required
responding to the new color, the positive affect manipulation reduced the response
time costs of responding to incompatible stimuli compared with the costs shown by
participants in a neutral mood. However, contrariwise, in the condition where the
targets were in a previously familiarized color, positive mood increased the costs of
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 1 369
cortex before one receives an instruction cue to either switch or stay—that is, before
one knows what the immediately upcoming task requirements will be—systematically
relate to, or predict, one’s performance on that task?
Leber and colleagues (2008) found that the answer was clearly “yes.” A pattern of
decreasing switch costs with increasing neural activity during the brief (precue)
window was observed in a number of brain regions, including medial and lateral
prefrontal cortex, posterior parietal cortex, anterior cingulate cortex, and right
anterior insula—all regions that previously have been reported as involved in task
switching and the maintenance of task sets (Dosenbach et al., 2006; see also the
discussion in the “Between Tasks” section of Chapter 9 on the causal role of right
insular cortex and anterior cingulate in triggering hierarchical control). Subcortical
structures, including the basal ganglia and superior colliculus, also showed this
pattern, with increasing pretrial neural activity systematically related to enhanced
task performance on the switch trials, suggesting improved task set reconfiguration
on the trials demanding a switch in task. Equally notably, however, there was evidence
that this increased activity in some regions was associated with slower (not faster!)
responses on trials that then required staying with the current task, rather than
switching. These findings again suggest, consistent with proposals by several theo-
rists, that there is a trade-off between cognitive flexibility and cognitive stability: Here,
the increased ability to respond quickly and accurately to a trial requiring a switch in
one’s current task set was accompanied by a moderate (though in some instances,
statistically significant) decrease in the effectiveness (speed) with which one responded
to a task that was the same (repeated) from a previous trial.
result of a single cerebral vascular accident. They placed participants into one of three
groups based on the predominant location of their lesion: frontal lesion, basal ganglia
lesion (i.e., caudate nucleus, putamen, and anterior limb of the internal capsule), or
posterior lesion. They found that the frontal lesion and basal ganglia lesion groups
showed marked and comparatively similar impairments in flexibility on the Wisconsin
Card Sorting Test. On this “reactive flexibility” task both patients with frontal lesions
and those with lesions in the basal ganglia showed a large number of perseverative
errors and difficulty in shifting set in response to the changing externally provided
feedback cues that followed changes in the (currently operative) categorization rules.
In contrast, the two lesion groups differed on the “spontaneous flexibility” measure
provided by the Alternative Uses Task. On this measure, the frontal lesion group was
severely impaired, but the basal ganglia lesion group was only moderately impaired
(performing similarly to the posterior lesion group) at generating alternative uses.
On the Alternative Uses Task, the frontal lesion patients provided many
responses, but these were of low accuracy. Frontal patients had difficulty in suppress-
ing responses that were salient but conventional uses of the objects. All of the basal
ganglia lesion patients that were tested had focal structural damage to the dorsolat-
eral head of the caudate, to the anterior limb of the internal capsule, and to the rostral
portion of the putamen; however, selective damage to the putamen alone did not
impede set shifting in one patient. Given these findings, Eslinger and Grattan (1993)
argued that “it is the region of the head of the caudate and anterior limb of the
internal capsule, together with their major projection site in the globus pallidus, that
provide the subcortical neural architecture for reactive flexibility” (p. 25) and that
“abnormal activation in bilateral frontal-basal ganglia circuits may underlie some of
the extreme forms of inflexible or rigid cognition” (p. 26).
Eslinger and Grattan (1993) suggested that the reason that the frontal lesion
patients were particularly impaired on the measure of spontaneous flexibility
(accuracy rate of 12% compared with 60%–89% accuracy in the other groups) was
that the Alternative Uses Task required the individual to “access various classes and
categories of knowledge in novel ways, bypassing more automatic or conventional
strategies.” In particular, the Alternative Uses Task appeared to be mediated by
frontal-cortical interactions rather than frontal-striatal interactions, and it draws on
multiple processes:
The conventional uses of objects are obviously of higher salience than more
remotely associated and less common alternate uses. Successful spontane-
ous flexibility, therefore, may require several elements. Objects need to be
represented as ideas rather than concrete stimuli, and strategic transforma-
tions of knowledge must be formulated to supersede the most prominent
semantic linkages and re-define the possible functions of an object. (Eslinger
& Grattan, 1993, p. 25)
Further evidence for the importance of the distinction between reactive versus
spontaneous flexibility—and the key role of dopaminergic modulation in both—was
provided by an imaginative approach adopted by Tomer and colleagues (2007). These
researchers sought to evaluate effects of dopamine on spontaneous flexibility (assessed
372 BRAIN AND ENVIRONMENT
by the Alternative Uses Task) versus reactive flexibility (assessed by the intra/extradi-
mensional set-shifting task from the Cambridge Neuropsychological Test Automated
Battery, Robbins et al., 1998) in individuals with Parkinson’s disease. However, these
researchers also capitalized on the observation that, in many individuals with
Parkinson’s disease, the onset of their illness is asymmetric. Often the disease first
more severely affects motor functions on either the left side of the body (reflecting
greater loss of dopamine in the right cerebral hemisphere) or the right side of the body
(reflecting greater loss of dopamine in the left hemisphere).
Consistent with previous studies, Tomer et al. (2007) found that, relative to
controls, individuals with Parkinson’s disease were impaired on both the spontaneous
and reactive flexibility tasks. However, asymmetric onset of the disease modulated the
effects on spontaneous flexibility. The left-onset group, who thus had greater loss of
dopamine in the right hemisphere, showed greater impairment on the spontaneous
flexibility measure, generating fewer correct responses and also making significantly
more errors on the Alternative Uses task than did the other groups. These results are
consistent with neuroimaging findings (Vandenberghe et al., 1999) that this or
similar tasks may be more strongly mediated by the right than the left hemisphere
(see also the section on “Brain Correlates of Insight Problem Solving” in Chapter 9).
In addition, medicated patients with right-sided onset (reflecting greater dopamine
loss in the left hemisphere) showed more errors on the reactive flexibility task, par-
ticularly more reversal errors. Thus, both medicated patients with right-sided onset
and medicated patients with left-sided onset showed more errors, but on different
tasks. Given the evidence for the acute sensitivity of cortical regions to an optimal
level of dopamine (reviewed earlier in this chapter), Tomer and colleagues (2007) pro-
posed that, for patients with asymmetric symptoms: “relatively early in the disease
process when dopamine deficit in the less-affected hemisphere is mild [. . .], optimal
dopaminergic medication (as determined by improved motor function) may involve
over-medication of the less-affected hemisphere.” On this interpretation, for example,
the errors on the Alternative Uses task in the left-onset group may have resulted from
a “hyper-dopaminergic state” in the left hemisphere, perhaps reflecting the patient’s
difficulties in maintaining and imposing the appropriate task set.
Other tasks of verbal fluency—such as letter and category fluency in which
participants are asked to generate words that, for example, begin with particular
letters (e.g., F, A, S) or belong to specific categories (e.g., animals, fruits, different types
of weather)—have been argued to draw on both automatic processes and strategic,
controlled processes. Automatic retrieval processes are proposed to be comparatively
more important in the production of words “within clusters,” that is, groups of words
that share semantic or other features. For example, the production rate of words
within a category or cluster tends to be quite constant, “consistent with the view that
the retrieval of words within semantic or phonological fields (or clusters) proceeds
relatively automatically [. . .] without much central executive involvement” (Rende
et al., 2002, p. 311). In contrast, controlled central-executive dependent processes
are proposed to be more important during strategic search for words that meet the
specified constraints (e.g., the instructions for the letter fluency task often state
that the words should not be proper nouns such as the names of cities or places) and
when attempting to identify new subcategories of potential candidate words and in
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 1 373
Yet goal neglect is not unique to individuals with brain damage: It can sometimes
be observed in everyone, and in some situations can occur quite frequently. In the
Multiple Errands task, for example, all of the patients, but also 5 out of the 9 control
participants failed to follow one of the task rules by neglecting on at least one occasion
to tell the experimenter when they had purchased an item in a shop. Failures to
consistently abide by all of the “rules” for a given context were also apparent in
the average number of errors on the Multiple Errands task made by the control
participants.
Recent work suggests that goal neglect is more likely to be observed if the activity
that we are currently attempting to perform differs in some respects from one that we
had performed in the same situation earlier, so that there are competing alternatives
for guiding what we might do (J. Duncan et al., 2008), particularly if the situation is
such that one of the responses we need to make is much more frequent than another
response (Kane & Engle, 2002). Another key determinant of whether goal neglect
occurs is the level of complexity of the task, including all of the facts, rules, and
requirements involved (J. Duncan et al., 2008; J. Duncan, 2010). As the complexity of
the overall “task model” incorporating these components increases, it becomes
increasingly likely that one of the task components will be “lost” from consideration—
and thus that one’s further actions will be based on this more simplified model that
lacks an important constraint for correct task performance.
The likelihood that individuals will show goal neglect on an experimental task is
strongly positively correlated with their performance on novel abstract reasoning
tasks that provide measures of “fluid intelligence,” such as series completion or
progressive matrices in the Cattell Culture Fair test (J. Duncan et al., 1996; J. Duncan
et al., 2008). Using a relatively simple task in which individuals were required to switch
between one rule and another rule, Duncan et al. (1996) found that goal neglect was
quite common in individuals who scored more than one standard deviation below the
mean on the Culture Fair Test, but it was absent in those scoring more than one
standard deviation above the mean. Tasks such as progressive matrices and series
completion themselves represent problems in which a number of different situational
constraints or rules must first be identified (based on the particular problem pre-
sented), and then must be “kept in mind” in working memory as one evaluates what
the next item in the series might be that would appropriately conform to all of those
constraints (Carpenter, Just, & Shell, 1990; Kane & Engle, 2002; see Fig. 9.4 for a
related example and the section on “Analogical and Relational Thought” in Chapter 9
for additional discussion).
This ability to keep multiple aims and constraints in mind has been termed “execu-
tive attention” by Kane and Engle (2002, p. 638), and it has been characterized by
these authors as the “psychological core of the statistical construct of fluid intelli-
gence, or psychometric Gf.” More specifically, they define “executive attention” as “a
capability whereby memory representations are maintained in a highly active state in
the presence of interference” where these representations “may reflect action plans,
goal states, or task-relevant stimuli in the environment.” This capability is especially
critical under conditions of interference or response competition that could yield
incorrect retrieval, and that therefore “set the occasion for relying on active mainte-
nance of information” (p. 638).
376 BRAIN AND ENVIRONMENT
In this study, not only prefrontal cortex but also bilateral parietal cortex played an
important role in mediating task performance on the difficult (high interference)
working memory trials, and bilateral parietal cortex was likewise a strong predictor of
the relation between fluid intelligence and behavioral performance on those trials.
A recent large-scale investigation of both structural and functional activity correlates
of this same fluid intelligence task (Raven’s Advanced Progressive Matrices), versus a
crystallized intelligence measure that draws on longer term knowledge (the Wechsler
Adult Intelligence Scale-Revised), likewise demonstrated that the frontal-parietal
network assumes a particularly important role in novel on-the-spot problem solving
(Y. Y. Choi et al., 2008; K. H. Lee et al., 2006). These researchers found that functional
activity differences, particularly in the frontal-parietal network, were correlated with
performance on the fluid-reasoning task. In contrast, structural differences (cortical
gray matter thickness), particularly in left temporal cortex, in regions that may be
involved in processing semantic information (to be discussed in Chapter 9), were
especially strongly correlated with the measure of crystallized intelligence. Multiple
linear regression analyses showed that whereas the overall amount of variance
explained by the structural brain correlates was greater for the crystallized measure
(37%) than for the fluid measure (22%), the reverse was true for the measure of fluid
intelligence. Functional correlates explained more of the variance in fluid on-the-spot
reasoning (31%) but less of the variance in crystallized (20%) intelligence.
In each of these studies, and in several further investigations (e.g., Colom et al.,
2007; Geake & Hansen, 2005; Prabhakaran et al., 1997), not only prefrontal cortex
but also bilateral parietal cortex played a significant role in mediating task perfor-
mance on working memory and fluid intelligence tasks. Although, thus far in this
chapter, we have predominantly focused on the key role of the prefrontal cortex in
enabling flexible cognitive control, the prefrontal cortex clearly does not operate
alone. There is very strong evidence for the important interactive relations between
prefrontal regions and parietal cortex (the frontal-parietal network) in sustaining
flexible online manipulation and updating of information, and also, more broadly, for
interactions between prefrontal regions and other posterior regions such as occipital-
temporal cortex, involved in representing diverse forms of stimuli such as objects,
words, faces, and scenes.
Interactions between frontal and parietal cortex during tasks requiring working
memory and reasoning have long been noted. Based on a review of 37 neuroimaging
studies using tasks probing fluid and crystallized intelligence, reasoning, and games
such as chess, Jung and Haier (2007, p. 138) proposed a “parieto-frontal integration
theory.” In this theory, they suggest that interactions between association areas within
parietal and frontal cortex—“when effectively linked by white matter structures”—
such as the arcuate fasciculus (a white matter tract that connects the temporal and
frontal language zones)—“underpins individual differences in reasoning competence
in humans, and perhaps in other mammalian species as well.”
A graphic summary of the key brain regions that their review identified as
implicated in reasoning tasks is presented in Figure 8.7. The dark circles represent
predominantly left hemisphere associations and the light circles represent predomi-
nantly bilateral associations; the white arrow represents the white matter fiber tract
of the arcuate fasciculus.
378 BRAIN AND ENVIRONMENT
More recently, J. Duncan (2010) has similarly proposed that the “multiple-demand”
pattern of frontal and parietal activity is observed across a variety of tasks in which
the task goal is achieved by a series of focused stages or subtasks. Including particu-
larly cortex in and around the posterior part of the inferior frontal sulcus, the anterior
insula and adjacent frontal operculum, the presupplementary motor area and adjacent
dorsal anterior cingulate, and regions in and around the intraparietal sulcus, this
network is recruited to enable “focus on the specific content of a current cognitive
operation, rapid reorganization with changing context, and robust separation of
successive task stages” (J. Duncan, 2010, p. 177). Findings from single-cell data,
reviewed by Duncan, increasingly point to such reorganization arising from transi-
tions between changing coalitions of active neurons during different task epochs, such
that “in complex behaviour, transitions from one step to the next are managed by
corresponding transitions among widely distributed, largely independent patterns of
prefrontal activity” (Duncan, 2010, p. 174). Much of the single-cell data have come
from recordings in the posterior part of the lateral prefrontal cortex of the monkey;
similar data from possible homologs of other “multiple-demand” regions, such as the
intraparietal sulcus, are greatly needed.
In line with this emphasis on the important contribution of the functional
connectivity between frontal and posterior cortices, a recent study has also docu-
mented differences in functional connectivity that correlate with general measures of
intelligence—even under conditions when no specific task is being performed (see also
the section on “Between Tasks” in Chapter 9). Song and colleagues (2008) examined
spontaneous brain activity during a resting state in 59 healthy adult individuals, in
relation to their scores on the Wechsler Adult Intelligence Scale. They found that the
strength of the functional connectivity between the frontal, parietal, occipital, and
limbic lobes was significantly correlated with intelligence scores. In addition, stepwise
380 BRAIN AND ENVIRONMENT
This is important, since efficient hub nodes are more likely to have a stronger
effect on global network efficiency than less connected peripheral nodes.
Interestingly, these frontal and parietal regions overlap the often reported
functional default mode network, a dynamic resting-state network that is
suggested to play a key role in processes of human cognition, like the inte-
gration of cognitive and emotional processes […] monitoring the world
around us […] and mind wandering […]. Furthermore, also the structural
dynamics of these parietal and frontal brain regions have been previously
linked to intelligence. (Van den Heuvel et al., 2009, p. 7621)
association to the cue that they had learned earlier) or incorrect (the probe did not
match what they had associated earlier).
If the computer network pattern classifier—trained only on brain activity data
gathered during the long-term memory task—nonetheless was able to successfully
differentiate between the categories of stimuli (i.e., famous people vs. famous
locations vs. common objects) in brain activity data gathered during the short-term
memory task, this would provide strong evidence that the delay-period activity in the
short-term task was substantially similar to that from the long-term task. This out-
come would then persuasively make the case that the working memory task produced
the temporary reinstatement of long-term memory activity. And this is exactly what
was observed.5
An integrative but somewhat speculative overview of the complex dynamic interac-
tions between cortical regions in supporting short-term memory (and the many
potential sources of memory failures) is provided in Figure 8.8. Taken from a recent
review of short-term memory by Jonides and colleagues (2008), the diagram is multi-
faceted and complex, but it depicts very well the dynamically integrative cognitive and
neural processes involved in the processing and neural representation of an item in
memory over the course of a few seconds, during which the individual must keep track
of additional new incoming information. Figure 8.8 also helps to integrate findings
relating to sustained activity-related representation, such as the single-cell recordings
in the studies of visual categorization in the monkey discussed earlier in this chapter,
and more durable “long-term” representations of objects and knowledge located in
posterior association regions of cerebral cortex (to be discussed in Chapter 9).
In Figure 8.8, the cognitive events occurring across time are represented at the
top of the figure. The bottom of the figure delineates the task events (e.g., when each
stimulus is presented, and the delays between them). The middle region of the figure
depicts the corresponding neural events. The y-axis (discussed more fully later) broadly
represents the “extent and basis of neural representation.” In the cognitive task that is
here illustrated, three stimulus items, such as novel shapes, are presented, one after
the other, and the participant’s task is to remember the first shape. An initial novel
shape is presented for 700 milliseconds, followed by a 2-second delay, then the second
stimulus appears, followed by a delay, and then likewise the third stimulus, also
followed by a delay. Last, a probe appears, during which memory for the first item
must be accessed and evaluated.
The colored layers in the middle of the figure indicate the extent to which different
brain areas contribute to the representation of the item over time, including: prefron-
tal control systems (shown as dark gray), parietal attentional systems (light gray),
posterior high-level perceptual systems (dark purple), posterior low-level perceptual
systems (light purple), and medial-temporal binding systems (pink). The changing
depth of the layers represents the changing extents to which the ongoing represen-
tational processes draw upon a given cortical region. Additionally, the diagram differ-
entiates between representations sustained by active neuronal firing, such as single
cells in prefrontal cortex (shown by solid layers), and memory supported by short-
term synaptic changes (shown by hashed layers). According to this proposal, whereas
neuronal firing supports the perceptual encoding and active maintenance of a stimu-
lus representation that is within the focus of attention, short-term synaptic plasticity,
Prefrontal control systems Posterior high-level perceptual systems Representation by active neuronal firing
Parietal attentional systems Posterior low-level perceptual systems Representation by synaptic changes
Medial-temporal binding systems
5 Iconic memory
at stimulus offset 6 Active maintenance mediated
by frontal-parietal systems;
decay caused by stochastic drift
12 Cue-based parallel retrieval,
3 Speed-accuracy trade-off subject to proactive interference
in perceptual encoding
9 Focus shifts to second
stimulus; first stimulus 13 Frontal-parietal mediated
8
4
TASK
Stimulus Delay Second stimulus and delay Third stimulus and delay Probe
EVENTS
Figure 8.8. The Neural Bases of Short-Term Memory. Schematic overview of the complex and dynamic interactions between multiple
brain regions involved in supporting short-term memory for the first of three visually presented stimuli in a short-term memory probe paradigm,
and involving both representation by active neuronal firing, and representation by synaptic change. See text for detailed explanation. Reprinted
from Jonides, J., Lewis, R. L., Nee, D. E., Lustig, C. A., Berman, M. G., & Moore, K. S. (2008, p. C-1), The mind and brain of short-term memory,
Annual Review of Psychology, 59, 193–224, with permission from Annual Reviews. Copyright 2008, Annual Reviews. Note: See the insert for a
full-color version of this image.
384 BRAIN AND ENVIRONMENT
this phase, (8) contributions from short-term synaptic potentiation, reflecting the
changing connection weights between brain regions, also occur in parallel, helping to
sustain both the representation of the item, and the item-context association.
When the second of the three stimuli is presented (9), the focus of attention rapidly
shifts to the new stimulus, and the active firing of the neural pattern of the first target
stimulus ceases. At this point, (10) the memory for the first stimulus is entirely reliant
on the changed synaptic connection weights and is vulnerable to disruption from the
active neural patterns relating to the second and third stimuli that are presented.
Additionally, as the first item remains outside of attentional focus, (11) other biochem-
ical processes may contribute to the decay of short-term synaptic enhancement.
Presentation of the probe, signaling to the participant that his or her memory for
the first item must now be accessed and evaluated, initiates (12)—a cue-based retrieval
of the target. This entails both strategic processes relying on active firing in frontal
and parietal regions and also a reinstantiation of representations of the target in
higher and lower order posterior perceptual regions and of the item-context associa-
tions in medial-temporal regions.
In this complex and interactively dynamic portrayal of the many cognitive and
neural processes that contribute to ongoing thinking (see Jonides et al., 2008, for
additional elaboration), “working memory” is not viewed as a specialized system or
set of subsystems, each involving different sorts of content (e.g., spatial information
or verbal or phonological information). In this view, working memory involves the
flexible directing of attention to different sorts of information that can be stored in
multiple areas of posterior cortex. According to a similar account of working memory,
proposed by Postle (2006):
and so on. Furthermore, the number of different ways in which information is repre-
sented may influence the different types of operations and sorts of problem-solving
activities that we can apply, so that “the ability to represent an item (or a piece of
information) in multiple codes, despite the unimodal channel by which it may have
been perceived, should facilitate one’s ability to manipulate or transform the repre-
sentation of this information” (Postle, 2006, p. 31). Thus, “thinking with our senses”—
involving our efforts to imaginatively link and richly interconnect stimuli and events
in multiple modalities—may be an essential contributor to working memory capacity,
and thereby to fluid and flexible thinking more generally.
The contributors to an “agile mind” potentially involve all areas of the brain that
contribute to representational, sensory, or action-related functions. This perspective
also suggests that the functional connectivity between prefrontal cortex and posterior
regions should be an important determinant of working memory performance
(Sakai et al., 2002) and that how effectively we encode information may play a central
role in boosting flexible thinking (e.g., Bor et al., 2003; Rypma & D’Esposito, 1999).
In addition, this view is entirely consistent with recent evidence reported by Jaeggi
and colleagues (2008) showing that training individuals in tasks that challenge their
current level of working memory capacity—through multimodal training that is
systematically titrated to the individual’s current capacity—significantly bolstered
their performance on a standardized measure of fluid intelligence. That research,
together with several other studies documenting the benefits of attentional and
working memory training on flexible thinking, is highlighted in Chapter 11. Now,
however, we turn, in the next “companion” chapter, to also explore some of the neural
bases that enable comparatively more spontaneous (rather than controlled) and more
specific (rather than abstract) modes of thinking that are equally fundamental to our
“agile minds.”
9
Brain Bases of Levels of Specificity
and Levels of Control, Part 2
Concepts and Intuition, Resilience, Novelty,
and Exploration
Perhaps
The truth depends on a walk around a lake,
A composing as the body tires, a stop
To see hepatica, a stop to watch
A definition growing certain and
A wait within that certainty, a rest
In the swags of pine-trees bordering the lake.
—Wallace Stevens (“Notes Toward a Supreme Fiction,”
1954/1990, p. 386)
387
388 BRAIN AND ENVIRONMENT
semantic knowledge and concepts in the brain. Although much remains unknown,
conjunctive findings from neuropsychological, neuroimaging, and cognitive-behav-
ioral studies have provided crucial insights into the nature of concrete (and multi-
modal) representations of concepts, and abstract (and amodal) representational
networks and their interrelations in our brain. Subsequent sections focus on the
networks involved in enabling analogical and relational thought, and in intuition and
insight. Turning to broader cognitive effects that arise from fluctuations in our level
of current arousal, or stress, the contributions of noradrenaline/norepinephrine in
the process of accessing semantic knowledge that is only remotely or more distantly
related to a problem or task at hand are highlighted.
These sections are followed by a consideration of the importance of the nature of
brain activity and the patterns of brain connectivity that are present during times of
“nondirected” and “spontaneous” thinking. Activity in what has come to be termed
the “default network” is increasingly recognized as an important player in adaptively
creative cognition and imagination. Research focused on the functional roles of this
network is providing an essential corrective to a too unilateral emphasis on directed
and intentional processing in enabling optimal mental agility. This section, together
with the previous sections of the chapter, explicitly aims to counter the heavier
weighting on deliberate and controlled processing that was true of Chapter 8. Titled
“Between Tasks: Thinking about the Past, Imagining the Future, and our Ever-Active,
Salience-Detecting and Network-Changing Minds,” the section also explores recent
proposals regarding what brain regions or network(s) of brain regions might assume a
role in switching between the central executive versus default networks. It highlights
accounts that right frontoinsular cortex and dorsal anterior cingulate cortex may be
part of a salience-detecting network that “unites conflict monitoring, interoceptive-
autonomic, and reward-processing centers” (Seeley et al., 2007, p. 2352)—and so may
be optimally situated to orchestrate such switching.
The last three sections of this chapter bridge forward, to the continual interactive
influences of our broader environment in shaping our minds and brains that are the
topic of Chapters 10 and 11, and also backward to earlier chapters on motivation and
emotion. Two sections explore the brain bases of “bouncing back” or resilience, and of
adaptive responding to novelty, respectively. The section on resilience draws attention
to the top-down influence of ventral medial prefrontal cortex, the role of serotonergic
function, and the mechanisms by which physical exercise and certain early experi-
ences may promote resilience to stress; the section on adaptive responding to novelty
focuses especially on the role of the locus coeruleus–norephinephrine system in
novelty, reward, and exploration. The final section turns our attention to the dynamic
interplay of cognition, emotion, and motivation that determine behavioral approach
versus behavioral avoidance. The sorts of stimuli and the types of situations that a
person chooses to approach and what, instead, he or she seeks to avoid, is multiply
determined: by temperament, and learning, and environmental opportunity, as well
as by his or her sensitivity to differing sorts of rewards and risks. This then, provides
an especially fitting jumping-off point for Chapters 10 and 11 that focus on how
our day-to-day and our longer term (monthly, yearly, lifelong) choices of social,
cognitive, educational, and leisure pursuits either promote, or diminish, “brain paths”
to mental agility.
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 389
there is, before us, no pictorial information but only a word that is the referent of a
previously seen picture (e.g., Polyn et al., 2005; M. E. Wheeler, Petersen, & Buckner,
2000). Neuroimaging findings have also shown that the brain regions that are acti-
vated during visual mental imagery partially overlap with those that are activated
during actual perception (e.g., Grèzes & Decety, 2001; Kosslyn et al., 1999; Kosslyn,
Thompson, & Alpert, 1997; Mechelli, Price, Friston, & Ishai, 2004; O’Craven &
Kanwisher, 2000), suggesting that both mental imagery and vivid recollection of past
experiences may involve a form of “mental simulation” or “mental reenactment”
(see Gallese & Lakoff, 2005 and Kent & Lamberts, 2008, for review and discussion).
Direct explorations of the role of sensory-motor cortices in the representation of
concepts also support the view that concepts are, at least in part, represented in brain
regions that overlap with the regions that support perceiving and acting (e.g., Chao,
Haxby, & Martin, 1999; R. F. Goldberg, Perfetti, & Schneider, 2006; Martin, 2007;
Martin et al., 1995; Simmons, Martin, & Barsalou, 2005; Tranel et al., 2003;
see Thompson-Schill, 2003, for review). When we access and use concepts, neural
networks that code salient sensory-perceptual properties of the relevant objects, such
as an object’s color (Martin et al., 1995) or taste (e.g., Simmons, Martin, & Barsalou,
2005) are activated. For example, R. F. Goldberg et al. (2006) showed that when
participants were asked to determine whether concrete words possessed a given prop-
erty for each of four modalities, including color (Was it green?), sound (Was it loud?),
touch (Was it soft?), or taste (Was it sweet?), different brain regions were activated in
each case. Compared with a control task, in which participants were shown nonwords
(pseudowords) and asked to determine whether they contained a specific letter, during
the retrieval and verification of tactile knowledge (touch) a region in somatosensory
cortex (postcentral gyrus) was activated whereas during attempted retrieval of
information about the taste of objects a region in orbitofrontal cortex, known to be
involved in representing special aspects of taste and smell, such as flavor identity, was
activated. Similarly, different regions were activated for the verification of whether
the object was associated with a loud sound (auditory association cortex in the left
superior temporal sulcus, just inferior and posterior to primary auditory cortex) and
whether it was green (left middle temporal cortex, Brodmann area 37). Brain regions
involved in enabling our physical and motor interactions with objects, such as grasp-
ing, also are activated when we access concepts of tools or artifacts such as “hammer”
(e.g., Beauchamp & Martin, 2007; Martin, 2007; Moro et al., 2008; but see also Bedny
et al., 2008, discussed later), or our mental notions of everyday objects such as light
bulbs, globes, and buttons (Yee, Drucker, & Thompson-Schill, 2010).
Depending on the particular task paradigm, some of these findings might reflect
postconceptual processing such as strategic imagery. However, combined functional
magnetic resonance imaging (fMRI) and electroencephalogram (EEG) findings
reported by Kiefer and colleagues (2008) suggest that related perceptual information
also may be activated quite early in the process of conceptual access, and perhaps
largely automatically at least in some cases. They found that words that had been inde-
pendently rated as clearly possessing sound- or acoustic-related features (e.g., tele-
phone) elicited more activity in the auditory association areas of the left posterior
superior/middle temporal gyrus than did words that were not rated as having promi-
nent acoustic-related features. The amount of activity increased linearly as a function
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 391
of the rated relevance of the acoustic features to the words and was shown to partially
overlap with the regions of brain activity found when participants actually heard
both real sounds and acoustic noise. Notably, this differential activity in auditory
processing regions was found for visually presented words, during a word/nonword
lexical decision task that did not direct the participant’s attention to auditory
features, and the event-related potential (ERP) recordings showed that activity in
auditory-association cortex emerged quite early—beginning at about 150 ms after
word onset. The regions that showed differential activation by the conceptually related
acoustic features were in higher order auditory association cortex (not primary or
secondary auditory cortex), leading Kiefer and colleagues (2008) to emphasize that
this form of implicit and perhaps automatic activation of acoustic conceptual knowl-
edge seems to involve a partial reinstatement of brain activity from early perceptual
experience. Such partial reinstatement differs from actual perception or highly vivid
imagery, which is accompanied by a clear subjective phenomenal experience and
involves activation in primary and secondary auditory cortex.
To assess whether a given word or concept is associated with particular sensory
properties, such as sound or color, most experiments have relied on subjective ratings
provided by persons during a stimulus norms collection phase (either conducted by
the experimenters themselves or in large-scale normative work published by other
investigators), or on lists of the sensory-perceptual and other properties that people
generate in response to particular words or concepts (e.g., Cree & McRae, 2003;
K. McRae, Cree, Seidenberg, & McNorgan, 2005). Notably, however, there is at least
initial evidence to suggest that modality-specific activations in brain regions might
also emerge when, rather than using subjective ratings from participants concerning
the types of perceptual-motor features that are associated with a given noun, extremely
large sets of text are used, in combination with computational modeling techniques,
to extract more abstract intermediate semantic features. Textual analyses might be
used to determine, for example, how often a given word, such as “celery,” occurs within
about five words of the word “taste” or variants such as “tastes” and “tasting” in a
trillion-word text corpus. In a pioneering exploration by T. M. Mitchell, Just, and
colleagues (2008) such intermediate semantic features, computationally derived from
text alone, were found to predict that a verb such as “eat” would be associated with
neural activity in gustatory cortex, whereas a verb such as “run” would be associated
with activity in cortical regions related to body motion.
A further and related important point of generally broad agreement regarding the
complex question of “where” conceptual knowledge is “found” in the brain is that—for
at least a comparatively small number of concept or object categories, predominantly
involving concepts or objects that, from an evolutionary standpoint, may have high
levels of importance to our adaptive functioning—processing is preferentially special-
ized in particular brain regions. Although the precise characterizations of why, and
how, such specialization develops are less well agreed, several classes of objects appear
to have specialized processing regions. There is extensive evidence relating to the
specificity of visual object representation in posterior cortex, including particularly
regions that are specialized for the representation and processing of the categories of
faces (the fusiform face area; e.g., Kanwisher, McDermott, & Chun, 1997; Kanwisher,
2000; Rhodes, Byatt, Michie, & Puce, 2004), parts of the body (the extrastriate body
392 BRAIN AND ENVIRONMENT
area; e.g., Downing, Jiang, Shuman, & Kanwisher, 2001; Spiridon, Fischl, & Kanwisher,
2006), places (the parahippocampal place area; e.g., R. Epstein, Harris, Stanley, &
Kanwisher, 1999; R. Epstein & Kanwisher, 1998), and, somewhat more controver-
sially, visual word forms (e.g., L. Cohen et al., 2000; L. Cohen & Dehaene, 2004; Yarkoni
et al., 2008; but see also Price & Devlin, 2003, 2004). Neuropsychological evidence has
also repeatedly shown that lesions to the brain may give rise to disproportionate
impairments that concern either a particular modality or type of knowledge (e.g.,
visual or perceptual knowledge or function-related knowledge about how objects are
used and manipulated) or to category-specific semantic deficits (see Devlin et al.,
1998; Mahon & Caramazza, 2009, for review). In the latter case, patients show dispro-
portionate impairments in the ability to access and use conceptual knowledge relating
to one or more broad categories of concepts, most often the categories of animals,
fruits/vegetables, nonliving things, or other people (conspecifics), but this impair-
ment is then general, rather than modality specific. For instance, a patient may be
generally impaired in naming and answering questions about living animate things,
but not for nonanimals (e.g., artifacts, such as furniture or tools).
Innovative research on the ways in which nonhuman primates may represent
semantic knowledge has further pointed to across-species similarities in certain
higher order categorical differentiations between broad classes of concepts.
Comparisons of visual object category selectivity in the human versus monkey
(macque) inferior temporal cortex (Kiani et al., 2007; Kriegeskorte et al., 2008), using
analyses of representational dissimilarity based on fMRI in humans and single-cell
recordings in the monkey, suggest that at least broad categorical divisions between
animate and nonanimate things, and between bodies and faces, are also found in these
primates (raised in human houses, and then in zoos, before being brought to the labo-
ratory). Kriegeskorte et al. (2008, p. 1138) suggest that these behaviorally important
categorical distinctions “are so basic that their conservation across species appears
plausible,” such that evolution and individual development lead to a “common code”
of representational features in primate inferior temporal cortex. This common code
appears to involve both distinctions between key categories, and more continuous
similarity-based distinctions of individual exemplars within category clusters.
Thus, that particular cortical regions are differentially involved in the representa-
tion and processing of certain classes of stimuli, such as faces, is broadly accepted.
Nonetheless, ongoing points of debate and investigative effort concern both the
number and types (or origins) of the constraints that lead to these forms of represen-
tational specialization (e.g., Cree & McRae, 2003) and the precise role of learning or
expertise in such specialization (e.g., McKone, Kanwisher, & Duchaine, 2007). At least
partially overlapping regions in the fusiform face area may, for example, be recruited
during other tasks that require fine-grained within-category perceptual discrimina-
tions, as might be demonstrated by expert birders or car buffs—or even experts in
differentiating between entirely novel and newly learned individual entities and fami-
lies of creatures, such as so-called greebles (e.g., Gauthier et al., 1999; Gauthier et al.,
2000; Tarr & Gauthier, 2000. However, see Behrmann et al., 2005, for a surprising
finding showing that training a man with impairments in face and object recognition
to discriminate between greebles led to improvements in his recognition of greebles
but substantially increased his response times for recognizing individual faces of
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 393
differing outcomes (e.g., Pexman et al., 2007, found a large number of widely distrib-
uted regions in temporal, parietal, occipital, and frontal cortex, as well as precuneus
and posterior cingulate, to be more active for abstract than for concrete concepts, with
no regions more highly activated for concrete than for abstract concepts).
Many neuroimaging studies have shown that comprehension of verbs denoting
actions, such as “kick,” leads to increased activity in several regions of the posterior
lateral temporal cortex, including in, or near, a region of the brain that processes visual
motion (MT+), and the right superior temporal sulcus, important for the perception
of biological motion. On the one hand, these findings suggest that understanding
action verbs may activate visual-motion representations (e.g., H. Damasio et al., 2001;
Martin et al., 1995). On the other hand when Bedny and colleagues (2008) attempted
to test this account directly, they found that, although several regions of posterior
lateral temporal cortex showed greater activation to words that described actions than
to words that described objects, these regions did not overlap with visual-motion
regions. Additionally, activity was not greater for verbs that were independently rated
as having high levels of visual motion features (e.g., “to run”) than for verbs referring
to mental actions (e.g., “to think”), and it was equally low for nouns denoting animate
animals (e.g., “the cat”) that typically move and inanimate natural objects (e.g., “the
rock”) that do not.
A possible account of these findings is that developed by Kable, Chatterjee,
and colleagues (Kable, Kan, Wilson, Thompson-Schill, & Chatterjee, 2005; Kable,
Lease-Spellmeyer, & Chatterjee, 2002). These investigators have proposed that there
may be a concrete to abstract organizational gradient in motion representations.
According to this account, comparatively more concrete representations of visual
motion are represented in relatively more posterior occipitotemporal cortex, close to
human motion processing areas (MT/MST), whereas more abstract propositional
action information may be represented closer to the middle temporal gyrus. Using a
semantic judgment task in which participants were asked to choose which of two
presented action concepts (e.g., “shoveling” or “listening”) was most similar to a target
concept (e.g., “digging”), Kable et al. (2002) found there was greater activity for
judgments that involved action concepts, than for judgments that involved objects,
bilaterally in human motion areas (MT/MST) and in nearby areas of the middle tempo-
ral gyrus. However, this was found only when the task was performed using pictures
that depicted the relevant actions, and not for words that referred to actions. In addi-
tion, the neural activations in occipitotemporal cortex were found to be comparatively
more posterior when the task was relatively more difficult and likely required detailed
visual processing of the alternatives (Kable et al., 2005) but were more anterior (com-
pared to the human MT/MST homolog) when comparing activation for predicate meta-
phors that do not literally imply motion, such as “The man fell under her spell,” than for
literal motion sentences, such as “The child fell under the table” (Chen et al., 2008).
These and related findings suggest that both aspects of the way that conceptual
knowledge is probed (e.g., through pictures vs. words) and the specificity of the concep-
tual knowledge that is needed in order to meet task requirements (e.g., relatively effort-
less coarse-grained vs. more difficult detailed discriminations, or more metaphorical
vs. more literal interpretations) may modulate the extent to which comparatively more
abstract versus more perceptually anchored associative brain regions are recruited for
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 395
conceptual knowledge retrieval and judgments. These findings also fit well with other
cognitive-behavioral evidence relating to the sensory-perceptual grounding of concepts
(e.g., Solomon & Barsalou, 2004)—discussed previously in Chapter 4— showing that
the precise nature of a task (e.g., whether unrelated vs. semantically associated lures
are used) can influence whether the task is performed primarily through sensory-per-
ceptual simulation or predominantly on the basis of lexical-associative knowledge.
Returning to emphasize a point made in Chapter 4: “Although we have such richly
linked sensory-perceptual and sensory-motor networks of meaning, about simple
objects such as chairs and watermelons, sometimes we bring to mind only very small
and restricted subsets of what is there. Sometimes we make little connection to the
sensory-perceptual features, traversing the deep world of meanings largely through a
suspended ‘surface-net’ of words and associations between words.”
Another important ongoing point of debate concerns the question of whether our
knowledge of concepts is then entirely distributed, such that these distributed brain
regions, and their interconnections, comprise the entire neural basis of semantic
memory. Whereas according to some views, these modality-specific regions and their
various interconnections comprise the entire semantic network, other views argue
that there are both modality-specific and “amodal” regions that integrate and/or point
to or “index” conceptual features from across the various modalities. In the conceptual
topography theory proposed by Simmons and Barsalou (2003), for example, although
modality-specific knowledge is represented in sensory-motor areas, there are also
across-modality “convergence zones,” for example, in the anterior ventromedial tem-
poral lobe (in particular, in perirhinal cortex). As in the convergence zones earlier sug-
gested by A. Damasio (1989; see also Meyer & Damasio, 2009), these cross-modality
convergence zones are thought to integrate and bind complex combinations of con-
ceptual features.1
Similarly, and in contrast to the “distributed-only view,” in the “distributed-plus-
hub” view proposed by Patterson and colleagues (2007), the sensory, motor, and lan-
guage-specific aspects of conceptual knowledge are necessary, but not sufficient. This
account proposes that, in addition to the various modality specific regions and their
interconnections, there also is a further amodal region, or “hub,” located in the ante-
rior temporal lobes. According to the distributed-plus-hub view, “in addition to direct
neuroanatomical pathways between different sensory, motor and linguistic regions,
the neural network for semantic memory requires a single convergence zone or hub
that supports the interactive activation of representations in all modalities, for all
semantic categories” (Patterson et al., 2007, p. 977).
A schematic depiction of the “distributed-only” and “distributed-plus-hub” views is
provided in Figure 9.1. Whereas on both views, the cortical semantic network is
broadly distributed, and partly organized in accordance with the neuroanatomy of
sensory, motor, and linguistic systems, the views differ in the forms of connectivity
they propose. As characterized by Patterson and colleagues, the distributed-only view
(panel a) involves connections between modality-specific cortical regions (shown in
green) that can be “gated” by the current task demands. For example, if the partici-
pant’s task were to name a visually presented line drawing of a familiar object, then
activation would flow from a representation of the object’s shape to its name (right-
side panel). In the distributed-only view, the associations between different pairs of
396 BRAIN AND ENVIRONMENT
Task
Task-
dependent
representation
Task-
independent
representation
Task
Shape
attributes (e.g., sound and action) are encoded in multiple different neuroanatomical
pathways. In contrast, in the distributed-plus-hub view (panel b), each of the modal-
ity-specific regions also is connected to a shared, amodal “hub” in the anterior tempo-
ral lobes (shown in red in panel b, with connections from this region to each of the
modality-specific regions shown in red). In addition, at this “hub stage,” it is proposed
that the associations between different pairs of attributes, such as shape and name,
shape and action, or shape and color, “are all processed by a common set of neurons
and synapses, regardless of the task” (Patterson et al., 2007, p. 977). This network is
thus a “convergent network” rather than a “gating network.”
The single most important source of evidence in support of the distributed-plus-
hub view comes from neuropsychology—and involves the nature of the impairments
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 397
type of object that the participant was asked to name. In contrast, stimulation to left
inferior parietal lobule—known to be involved in representing information about
human-made objects and tools that can be manipulated—elicited a category-specific
naming impairment. Stimulation to the left inferior parietal lobule led to significantly
slower naming times for objects that were highly manipulable, but it did not signifi-
cantly slow the naming of objects that were low on this “manipulability” dimension.
As observed by Pobric et al. (2010, p. 967), these results, “fit squarely with the hub-
and-spoke model of semantic memory” and provide support for the conclusion that
both the amodal hub of the anterior temporal lobe and modality-specific association
“spokes” contribute to semantic representations:
Because the ATL hub is involved in the translation and deeper encoding of
pan-modal information sources, the representations become modality
invariant […] and thus they are involved in conceptualization for all types of
category. In contrast, modality specific information contributes only to the
subset of concepts that are experienced in that modality. Unlike other modal-
ity specific areas, [the inferior parietal lobule] is an ideal test region given
that there is an almost binary division of praxis experience between manipu-
lable objects and other concepts. (Pobric et al., 2010, p. 967)
(e.g., a robin and a kingfisher) because these objects are represented with quite similar
patterns of activity in the anterior temporal lobe. In contrast, there would be less
disruption for discriminating between conceptually unrelated items (e.g., a robin and
a yacht) because these are represented with dissimilar patterns of activity.
According to the distributed-plus-hub view (e.g., T. Rogers & Patterson, 2007),
whereas the neural representations in modality-specific regions of the brain capture
similarity based on relevant surface or sensory-perceptual features (e.g., similar visual
shapes), neural representations in the anterior temporal cortex instead capture simi-
larity based on conceptual features, even if the conceptually similar items do not share
many similar surface features (e.g., a flamingo and a hummingbird). On this account,
items that are “the same kind of thing” are represented as similar—even if they differ
greatly in visual appearance, and so on. Given that conceptually similar things are
represented by very similar patterns of activity across distributed neurons, naming a
particular bird as a “robin” requires the anterior temporal lobe hub to:
… instantiate the robin representation almost exactly, as the name does not
apply to other kinds of birds, many of which nevertheless have representa-
tions that are very similar to the robin. To name the same item “bird,” how-
ever, the robin pattern need not be instantiated exactly. Because the name
applies to all birds and all birds share similar representations, it is only neces-
sary for the hub to find a representation that is sufficiently “bird-like” to acti-
vate the name. Thus, small distortions of the “robin” representation—perhaps
resulting from anterior temporal lobe atrophy—will prevent the network
from retrieving the robin’s specific name (and other properties that differenti-
ate it from other birds) without disrupting the retrieval of properties that are
common to birds. A similar explanation extends to the interpretation of the
functional imaging results, if one assumes that a stronger metabolic response
in the anterior temporal lobe occurs in tasks that require the differentiation of
highly overlapping representations. (Patterson et al., 2007, p. 984)
Stated differently, the overlapping manner in which similar concepts are repre-
sented in the semantic system, leads to a greater likelihood that, following disruption
of the system through disease or other means, highly specific conceptual discrimina-
tions will be impaired, even though more general (less specific) discriminations can
still occur. Whereas under normal conditions, the conceptual similarity structure
“promotes semantic generalization and induction,” when anterior temporal regions
are damaged, then “the same principle of semantic organization militates against
retrieval of properties idiosyncratic to a specific concept”:
Because such properties are not shared by closely neighboring concepts, the
intermediating representations in the anterior temporal cortex must be spec-
ified with great precision in order to generate the correct response elsewhere
in the cortical network. As these representations degrade in semantic demen-
tia, it becomes increasingly difficult to settle upon precisely the right pattern,
and hence, to retrieve detailed semantic information. For more general infor-
mation, the anterior temporal lobe system can yield the correct response, so
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 401
long as it finds itself in the right representational ballpark, because all neigh-
boring representations will tend to produce the same correct response in the
rest of the network. (T. Rogers et al., 2006, pp. 209–210)
The computational model developed by T. Rogers and colleagues also led to a pre-
diction that, while contrary to what would be expected on many models of semantic
memory organization, is consistent with the pattern of changes in representational
level of specificity found in semantic dementia. In healthy adults—and also in chil-
dren—a “basic-level” advantage is very often observed, such that we can more rapidly
and more accurately identify objects at a “basic” level (e.g., as a dog, or a cat) than at
either a superordinate level (e.g., as an animal) or at a subordinate level (e.g., as a
golden retriever). Although many different theoretical accounts have been forwarded
for this pervasive and highly reliable effect (e.g., Jolicoeur, Gluck, & Kosslyn, 1984;
G. L. Murphy & Smith, 1982; Rosch et al., 1976), it appears to be at odds with the
findings from semantic dementia patients, who do not consistently show a basic-level
advantage but may name and classify items at a superordinate level (e.g., animal).
T. Rogers and Patterson (2007) predicted that, in healthy adults, the basic-level
advantage could be eliminated if conditions were such that they needed to respond
on the basis of a poorly specified semantic representation—such as might be true of
individuals in the relatively more advanced stages of semantic dementia.
In line with this prediction, when healthy adults were required to make semantic
classification decisions exceedingly rapidly, using what is known as a response dead-
line procedure, this was just the outcome that was observed. Participants first were
shown a name of an object, with the name at a subordinate, basic, or general category
level, and then were shown a matching or nonmatching color photograph and were
asked to decide whether the photograph matched the name. A series of regularly
spaced beeps presented after the name, at one of three tempos, prompted participants
to respond at one of three different deadlines (individually titrated to their perfor-
mance rate in an earlier control task): slow, medium, or fast. When participants were
required to respond very quickly, then—as predicted, and consistent with the findings
from patients with semantic dementia—participants were the most accurate for the
general category decisions, and least accurate for the specific decisions, with accuracy
for the basic-level decisions intermediate between these superordinate and subordi-
nate levels. These results are shown in Figure 9.2, separately for the three deadline
speeds (slow, medium, and fast). In contrast, when no deadline was imposed (shown as
“Exp. 1” in Fig. 9.2), then the usual “basic level” advantage in accuracy was observed.
A schematic depiction of why the connectionist model predicted these outcomes is
shown in Figure 9.3. In the diagram, each point indicates the representation of
a particular item (which, in the parallel distributed model, is itself a “point” in a mul-
tidimensional space of multiple neuron-like processing units). The proximity between
the points indicates the degree of conceptual similarity between the corresponding
representations: thus, a canary is close to other instances of birds but less close to
other sorts of animals. Because it applies across a very broad range of semantically
related items, the superordinate name (e.g., “animal”) normally begins to activate
earlier than the basic-level name. However, the broadly spaced representations for
animal (shown within the larger area designated by the broken line in the left-hand
402 BRAIN AND ENVIRONMENT
RTs for all trials meeting deadline Accuracy for all trials meeting deadline
1100
General 2.90 General
1000 Basic Basic
Specific
2.70 Specific
900
2.50
RT (ms)
800 2.30
d’
700 2.10
600 1.90
500 1.70
400 1.50
Exp 1 Slow Med Fast Exp 1 Slow Med Fast
RTs for trials consistently meeting deadline Accuracy for trials consistently meeting deadline
1100 2.90
General General
1000 Basic 2.70 Basic
Specific Specific
900 2.50
RT (ms)
800 2.30
d’
700 2.10
600 1.90
500 1.70
400 1.50
Exp 1 Slow Med Fast Exp 1 Slow Med Fast
panel of Fig. 9.3) do not foster a lot of generalization across one another. Therefore,
the name “animal,” although it begins to be activated first, also activates quite slowly.
In contrast, the basic-level name (e.g., “bird”) does not begin to activate quite as early.
Yet it lives in a “neighborhood” with many other nearby conceptually similar instances
(that is, many other types or instances of birds). Therefore, although activation of the
name “bird” begins a bit later than activation of “animal,” it accelerates more rapidly
and reaches full activation sooner than does the superordinate name (see right panel
of Fig. 9.3). A highly specific subordinate name, such as “canary,” does not begin to be
activated until the internal representational state is quite close to the correct repre-
sentation, leading to the most slowly activated response.
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 403
Threshold
Canary
Bird
Animal
Canary
Bird
Animal Time
Collectively, these findings argue that, despite the frequent absence of activation
differences in the anterior temporal lobes during semantic memory tasks when using
404 BRAIN AND ENVIRONMENT
fMRI, there is very strong convergent evidence from other brain imaging methods and
from neuropsychological investigations (e.g., see also Lambon Ralph et al., 2010) that
these regions play a critical role in semantic memory—most likely involving amodal
or more abstract multimodal associative connections of concepts. Nonetheless, the
precise nature of these relatively abstract associative knowledge connections remains
to be more fully explored, and the full empirical picture is not as entirely unmixed as
thus far portrayed. Three interrelated questions, in particular, need to be addressed, to
more fully integrate the distributed-plus-hub view with additional neuropsychologi-
cal, neuroimaging, and other findings that, at least on the surface, seem not fully con-
gruent with the account.
First, as elaborated in the following paragraphs, additional work is needed to exam-
ine possible subclassifications within more abstract concepts or socially relevant con-
cepts that might differentially call upon some subregions of the anterior temporal
lobes. Second, additional work is needed to articulate the relations between anterior
temporal lobe amodal semantic representations and the considerable evidence, from
neuroimaging, neuropsychology, and comparative neuroanatomy, for the involvement
of these regions in socioemotional processing (Olson et al., 2007; L. A. Ross & Olson,
2010). Third, these regions are also implicated in the processing of “unique” entity
information, such as that required in identifying and recognizing individual people
and landmarks (e.g., H. Damasio et al., 1996; Gorno-Tempini & Price, 2001; Tranel,
2006; Tsukiura et al., 2008). For instance, patients with semantic dementia that has
predominantly affected the left versus right temporal cortex also frequently show
deficits in recalling people’s names versus faces, respectively (e.g., Snowden et al.,
2004; Gainotti, 2007), and anterior temporal lobe resection surgery may lead to simi-
lar effects (Gloser et al., 2003; Tippett et al., 2000).
Simmons and colleagues (Simmons et al., 2010; Simmons & Martin, 2009) have
presented evidence that the anterior temporal lobes are particularly involved in the
representation of social knowledge. Based on findings from a neuroimaging study in
which individuals learned facts about people, buildings, or hammers (Simmons et al.,
2010), these investigators argue that, rather than acting as a domain-general hub, the
anterior temporal lobes work together with other regions frequently implicated in
social cognition, such as the medial prefrontal cortex, the posterior superior temporal
sulcus, the amygdala, and the precuneus/posterior cingulate, to support learning of
facts about others. Other researchers (e.g., Zahn et al., 2007) have provided neuroim-
aging evidence that the right superior anterior temporal lobe is involved in the repre-
sentation of abstract concepts that have social conceptual content (e.g., concepts such
as honor-brave) compared with concepts describing general animal functions (e.g.,
nutritious-useful); activity in this region further correlated with the richness of the
detail with which social concepts describe social behavior (Zahn, Moll, Paiva et al.,
2009; see also S. Green et al., 2010).
Activation in the anterior temporal lobes also has been frequently reported under
conditions in which individuals seek to infer the mental states or emotions of others
(see Olson et al., 2007, Table 3, for neuroimaging studies showing temporal pole acti-
vation in tasks involving mentalizing or theory of mind), or, indeed, when they engage
in inference processes relating to the animacy and intentionality of movements
depicted by abstract geometric shapes (e.g., Castelli et al., 2000; L. A. Ross & Olson,
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 405
2010). Furthermore, lesions to the anterior temporal lobe do not only lead to concep-
tual impairments but also to marked changes in social behavior (Zahn, Moll, Iyengar,
et al., 2009). Based on an extensive review of both nonhuman primate and human
findings, Olson and colleagues (2007, p. 1718) argue that the temporal pole has a role
in both social and emotional processing, including theory of mind and face recogni-
tion, “that goes beyond semantic memory” and propose that “the temporal pole binds
complex, highly perceptual inputs to visceral emotional responses.”
In line with these arguments, it might be noted that one of the few fMRI studies
that reported greater activation in the left anterior temporal pole for abstract words
than for concrete words (Noppeney & Price, 2004) involved a contrast between seman-
tic judgments for groups of abstract words that were arguably predominantly socioe-
motional in content (e.g., “conceit,” “arrogance,” “pride”; “wicked,” “evil,” “wrong”) and
concrete words with largely single-modality referents (e.g., “silver,” “gray,” “gold”; “par-
allel,” “cube,” “oval”). The comparative importance of the referential content of the
abstract words (denoting objects, events, or characteristics with high vs. with low
socioemotional relevance) versus the concrete words (denoting predominantly single
modality vs. more complex multimodality objects or actions) in these results is not
known, and it is one of the questions currently being explored in our lab using fMRI in
combination with multivoxel pattern analyses (Hoversten et al., in progress) that may
prove less susceptible to signal dropout than are more traditional fMRI analysis
approaches.
On the one hand, it is possible that, from a broader, more encompassing perspec-
tive, the unique entities, socioemotional processing, and amodal hub accounts are in
agreement. Amodal integration across modalities may also plausibly include integra-
tion of highly perceptual inputs with visceral emotional responses, and the processes
leading to identification of unique identities, such as a particular person, also involve
integration of input from multiple modalities—such as auditory or vocal expression—
that, likewise, is represented across several neural regions (e.g., Haxby et al., 2000).
Furthermore, the failure to experience expected socioemotional and visceral emo-
tional responses when seeing a highly familiar person, such as one’s spouse or parent,
may be associated with experiences of empathic disconnection and have been linked
to syndromes such as Capgras, in which the affected individuals believe that a seem-
ingly familiar person has been “replaced” by a look-alike imposter (Hirstein &
Ramachandran, 1997). Consistent with their subjective reports, despite conscious
recognition, individuals with this syndrome may show no autonomic response (change
in skin conductance response) to familiar compared with nonfamiliar faces (H. D. Ellis
et al., 1997; Hirstein & Ramachandran, 1997). Such disturbances in experienced
emotional connectedness to highly familiar faces, and related feelings of emotional
disconnection, have been associated with lesions or metabolic changes in the tempo-
ral lobe (e.g., Hudson & Grace, 2000; Lipson, Sacks, & Devinsky, 2003).
On the other hand, it is possible that more finely differentiated analyses, using
techniques such as single-cell recordings and fMRI adaptation paradigms that can, in
principle, uncover the neural composition of individual voxels (Bartels et al., 2008;
Goebel & van Atteveldt, 2009) will reveal interspersed but still spatially organized
subsets of neurons within the anterior temporal lobe relating to different combina-
tions of across-modality information. Neurons that prefer particular modalities, or
406 BRAIN AND ENVIRONMENT
The semantic impairments in stroke aphasia patients also were correlated with the
degree of executive dysfunction they demonstrated (for example, as shown by perfor-
mance on a complex visuospatial reasoning task), whereas semantic impairment and
executive dysfunction were not strongly associated in semantic dementia.
These differing patterns of impairment led Jefferies and Lambdon Ralph (2006) to
propose that “semantic cognition”—involving “our ability to use semantic knowledge
efficiently and accurately in all situations (i.e., all verbal and non-verbal receptive and
expressive activities)—requires two interacting elements.”
The first is a set of amodal semantic representations that are formed through
the distillation of information arising in various association areas specific to
particular input or output modalities […]. The anterior lobes are strongly
connected to all the cortical association areas […] and are thus a prime loca-
tion for this type of amodal data reduction. (Jefferies & Lambdon Ralph,
2006, p. 2143)
Although we know many different things about objects, the aspects that are
relevant for a particular task or context vary. Therefore there has to be flexi-
bility in the information being activated by the underlying amodal concept
to produce task-appropriate behaviour. (Jefferies & Lambdon Ralph, 2006,
p. 2144)
One final and related question of debate and continuing investigation concerns
the consistency in our concepts and associated neural representations across tasks,
across time, and across persons (e.g., Hoenig et al., 2008; Tranel, 2006 4). As noted in
Chapter 4, and also earlier in this section in the discussion of the representation of
concepts involving action (E. Chen et al., 2008; Kable et al., 2002; Kable et al., 2005),
the exact requirements of the task may modify the extent to which perceptually salient
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 409
properties are used or accessed. Recent work, for example, has shown that the extent
to which motor-related regions related to the mental representation of arm and leg
movements are recruited during the processing of action verbs depends on the context
(Raposo, Moss, Stamatakis, & Tyler, 2009). Greater activation in the relevant (arm vs.
leg) motor regions was observed when words were presented alone (e.g., “kick”) than
when the same words were presented embedded within brief literal sentences (e.g.,
“kick the ball”). However, activation was found, instead, in frontotemporal language
processing regions, and not in motor or premotor cortices, when nonliteral idiomatic
sentences (e.g., “he kicked the bucket”) were presented. This suggests that motor/pre-
motor related activation, in part, depends on factors such as how much emphasis is
placed on the relevant actions. More broadly, these and related findings suggest that
“access and integration of meaning is a flexible process, which depends on the senten-
tial context and [. . .] on the information that one needs to extract from the represen-
tations as a function of the cognitive task at hand” (Raposo et al., 2009, p. 395).
More enduring, cross-situational individual differences in how concepts are pre-
dominantly accessed, such as with accompanying perceptual information or primarily
in abstract lexical or verbal format, also need to be taken into account (cf. the discus-
sion in Chapter 2 and Chapter 3 of overly abstract or lexical processing in individuals
with clinical depression and excessive worry or rumination). For example, Kraemer,
Rosenberg, and Thompson-Schill (2009) found that individuals with self-reported
visual versus verbal styles of processing showed correspondingly correlated differ-
ences in activity in modality-specific processing regions of the brain during a task that
presented information in the “nonpreferred” modality. Individuals who scored rela-
tively higher on a tendency toward verbalization showed increased activity in a region
involved in phonological processing (left supramarginal gyrus) during trials in which
they needed to decide which of two pictured shapes (e.g., a picture of a green dotted
triangle or a picture of a red striped circle) was more similar to an earlier presented
shape (e.g., a picture of a red striped triangle); this pattern of brain activity in indi-
viduals prone to using a verbal processing style was not observed on trials in which
lists of words denoting the relevant features of the target (e.g., the words “orange,
circle, dots”) and the two alternatives (e.g., the words “circle, plaid, orange” versus
“dots, green, square”) were presented.
One interpretation of these findings is that those individuals with a verbal process-
ing style may have “recoded” the pictorially presented information into a verbal
format. Consistent with this interpretation, a contrasting pattern was found in indi-
viduals who scored relatively higher on a tendency toward using a visualization pro-
cessing style. These individuals showed increased activity in a visual processing region
of occipitotemporal cortex (right fusiform) during the verbal (word list) trials, but not
during the trials involving pictures—suggesting that these participants were recoding
the words into pictorial format.
Collectively, these and the other findings reviewed in this section emphasize that
the instantiation of semantic concepts in the brain is dynamically sculpted by multiple
factors, including not only the nature of the concept that is to be brought to mind, or
the particular task demands at hand, but also by more enduring predispositions in
how an individual spontaneously or most frequently processes meaningful informa-
tion. The findings have underscored the many levels of representational specificity
410 BRAIN AND ENVIRONMENT
In contrast, situations that require the integration of two or more relations that are
presented in a nonordered fashion cannot be readily understood in this way and
appear to require higher order reasoning. To infer the heights of the three respective
individuals from the statements, “Jane is taller than Mary,” and “April is taller than
Jane,” we need to keep in mind the relations of both Jane to Mary, and of April to
Jane, at the same time.
In an important neuropsychological assessment of relational reasoning, Waltz,
Knowlton, Holyoak, and colleagues (1999) contrasted the performance of patients
with the frontal variant of frontotemporal dementia with that of patients with the
temporal variant (i.e., semantic dementia patients), and matched control participants,
on several reasoning tasks. They used both a measure of deductive reasoning and a
measure of inductive reasoning that placed varying demands on the need to integrate
relational information. The measure of deductive reasoning involved a set of transi-
tive-inference problems, such as the height problems given earlier, that required par-
ticipants to evaluate either ordered (Level 1) or scrambled/nonordered (Level 2)
transitive inference problems involving three, four, or five people. The measure of
inductive reasoning was a visuospatial progressive matrices or pattern completion
task that similarly manipulated the number of relations that the participant needed to
simultaneously consider in order to select the appropriate alternative from six choices
(see Fig. 9.4 for an example). The simplest problems involved no relations and could be
solved by simple visual pattern matching (Fig. 9.4A), whereas one-relation problems
(Fig. 9.4B) required the test-taker to take into account a change in one stimulus dimen-
sion (e.g., spatial orientation, here involving reflection along the x-axis). Two-relation
problems (Fig. 9.4C) required that the problem solver take into account changes in
two dimensions (e.g., both the texture-pattern of the stimulus, here involving a solid
A B C
1 2 3 1 2 3 1 2 3
4 5 6 4 5 6 4 5 6
or checked pattern, and the shape of the stimulus, here involving the removal or
nonremoval of the upper-right quadrant from the depicted shape).
The results for both the transitive inference and the visuospatial pattern reasoning
tasks showed a markedly different pattern of performance in the three groups
(those with the frontal vs. temporal variants of frontotemporal dementia vs. normal
controls). On the one hand, the individuals with frontal damage performed quite
similarly to both the temporal lobe patients and to the normal controls when either
the transitive inference items were systematically ordered (Level 1) or the matrices
problem required consideration of only a single relation, or no relations. On the other
hand, the performance of the frontal damage patients was markedly impaired relative
to both the temporal lobe patients and the controls on the trials where multiple
(binary) relations needed to be simultaneously integrated, and it was not possible to
solve the task by processing one relation at a time. The frontal patient group was
unable to solve the two-relation transitive inference problems at a rate better than
chance performance. In contrast, the individuals with temporal damage were able to
solve these multirelational problems—even though, as expected, they showed signifi-
cant deficits on tests of semantic knowledge. Together, these dissociations, and other
findings, led Waltz and colleagues (1999, p. 123) to hypothesize that “the integration
of relations is a specific source of cognitive complexity for which an intact prefrontal
cortex is essential.”
Further neuropsychological and computational findings (e.g., R. G. Morrison et al.,
2004) and several neuroimaging studies (e.g., Kroger et al., 2002; Wharton et al.,
2000, discussed later) have provided strong convergent support for the central impor-
tance of prefrontal cortex—especially rostrolateral prefrontal cortex or lateral
Brodmann area 10, also known as the frontal pole—in relational integration. More
broadly, this region appears to be important in a wide variety of types of tasks in
which “the application of one cognitive operation (such as a rule) on its own is not
sufficient to solve the problem as a whole, and the integration of the results of two or
more separate cognitive operations is required to fulfill the higher behavioural goal”
(Ramnani & Owen, 2004, p. 190. See also Gilbert et al., 2006a, 2006b; Halford et al.,
1998, for review, and the section on “Neuroimaging Evidence for Hierarchical and
Functional Distinctions within Frontal and Prefrontal Cortex” in Chapter 8.)
To take one specific example, Christoff and colleagues (2001) found that, in healthy
adults, the rostrolateral prefrontal cortex was differentially activated when partici-
pants attempted to solve visuospatial progressive matrices problems involving two
relations compared with only one or no relations. Greater activity in this region was
not simply a matter of greater difficulty for the former problems. Christoff et al. (2001)
found that even after using a within-subject matching procedure to equate the three
different conditions on approximate response times and accuracy rates, activation in
left rostrolateral prefrontal cortex was specific to the 2- versus 1-relational compari-
son, and it was not found in the comparison of 1- versus 0-relational problems.
Studies by Kroger et al. (2002) and Bunge et al. (2009) pointed to similar conclu-
sions. Using a parametric manipulation of relational complexity, in which participants
needed to consider 0, 1, 2, 3, or 4 relations in a given matrix problem, Kroger and
colleagues (2002) demonstrated that, although regions in parietal and dorsolateral
prefrontal cortex showed increased activity both as a function of increasing relational
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 413
complexity and added distractors, a region in anterior left prefrontal cortex that
extended into BA 10 was selectively responsive to increasing relational complexity.
This more anterior left frontal region was particularly activated for the highest levels
of relational complexity and was insensitive to the number of distractors that were
present. More recently, using an analytically powerful paradigm involving identical
stimulus displays across conditions and a judgment task that always required a deci-
sion regarding the presence versus absence of a match, Bunge, Helskog, and Wendelken
(2009) likewise provided evidence that left rostrolateral prefrontal cortex assumes a
fundamental role in the integration of disparate visuospatial relations.
Each of these studies involved visuospatial stimuli. However, another important
form of relational reasoning is verbal analogical reasoning. In analogical problems, we
must find (or “abstract”) a higher order relation between a given (often familiar) rep-
resentation and another (sometimes novel) representation, finding a way in which the
two representations correspond to one another (Gentner, 1983; Holyoak & Thagard,
1989. See also the section on “Analogies, Similarities, and Such” in Chapter 3, as well
as Excursion 2, which considers the role of subcognitive mechanisms in analogical
thinking.) Bunge and colleagues (2005) contrasted the brain regions that were
recruited when participants decided whether two successive pairs of words were
semantically analogous to one another (e.g., “bouquet–flower” and “chain–link”)
versus a control task in which they decided if the two words in the second pair were
semantically associated with one another (e.g., “note–scale,” followed by “rain–
drought”). An instruction cue presented after the first pair of words and before the
second pair directed participants as to which task they should perform.
In agreement with the findings using visuospatial analogical materials, a region in
left frontal polar cortex (BA 10/11) was particularly responsive to the task manipula-
tion. This region demonstrated greater activity during the analogy task that required
relational integration than during the semantic association task that did not require
relational integration (see also Green et al., 2010). In contrast, a region in anterior left
inferior prefrontal cortex was more responsive to the degree to which the words within
a pair were strongly semantically associated with one another. This left anterior pre-
frontal region showed greater activity during trials involving words that were compara-
tively weakly associated with one another—and so were more difficult to retrieve. These
latter findings are consistent with the proposal, outlined in the previous section, that
anterior left inferior prefrontal cortex assumes an important role in retrieving relevant
semantic knowledge about and associations between stimuli. The pattern in frontal
polar cortex coheres with an interpretation in which an essential role of this region is to
help to integrate multiple retrieved relations (subsequent to their retrieval).
In the foregoing study by Bunge and colleagues (2005) the two pairs of words were
presented successively in time. Thus, in order to perform the analogical reasoning
task, the participants needed to keep the first word pair in working memory while
comparing it with the second word pair. A subsequent study (Wendelken et al., 2008),
in which all of the relevant terms that needed to be relationally integrated were pre-
sented together, extended and replicated these findings. Regions in bilateral (ventral)
rostrolateral prefrontal cortex were more active during a task in which participants
were asked to compare the two relations (e.g., Is shoe to foot as glove is to hand?–
“yes”) than in a task in which they were asked to complete a relation (e.g., Shoe is to
414 BRAIN AND ENVIRONMENT
foot as glove is to WHAT?”–“hand”). In the first task, one must retrieve the semantic
relationship that links each pair of terms, and then compare, map, or integrate those
relationships. In contrast, one can complete the second task by first retrieving the
relation between the first two items, and then using this retrieved relation to com-
plete the second word pair. Greater rostrolateral prefrontal cortical activation in the
former task than the latter is thus strong support for this region being particularly
important for the comparison of relations.
Together, these findings, and additional neuroimaging findings from developmen-
tal comparisons in humans (e.g., Wright et al., 2008) support the important role of
rostrolateral prefrontal cortex in comparing or evaluating relational information.
Such a role is consistent with neuroanatomical connectivity evidence that this most
anterior region of prefrontal cortex primarily interacts with other prefrontal cortical
regions, rather than with the posterior cortical regions that support conceptual knowl-
edge, and also with evidence relating to the cellular and dendritic properties of this
region. As underscored by Ramnani and Owen:
We may use this concept [of association horizon] to formally categorize our
notion of relevance. Relevance is differentially defined for each person, under
each set of circumstances, in terms of his or her event horizon. A person with
a wide horizon will consider some words, concepts, memories, or whatever
to be relevant, but a person with a narrow horizon might consider the same
items irrelevant, and the relative position of that person’s horizon may be
measured in terms of the commonness or remoteness of his or her associa-
tions. A creative person will have a wide horizon, an uncreative person a
narrow one. The horizon will determine the search process, in the sense that
no one will go outside his or her horizon because what is outside is not con-
sidered relevant. (H. J. Eysenck, 1993, pp. 151–152)
Tasks such as solving anagrams and compound remote associates may require a
broad search throughout the lexical/semantic network (Mednick, 1962) and thus have
416 BRAIN AND ENVIRONMENT
been used as measures of both insight and cognitive flexibility. Beversdorf and
colleagues showed that administering the drug propranolol—a central and peripheral
beta-adrenergic antagonist often used to counteract test or performance anxiety
(e.g., J. R. T. Davidson, 2006; Drew et al., 1985)—significantly facilitated anagram
performance latencies compared with when adrenergic agonists were administered
(Beversdorf et al., 1999), and also compared with when a beta-adrenergic antagonist
that has only peripheral nervous system effects (nadolol) was given (Beversdorf et al.,
2002). However, in neither of these experiments were the beneficial effects of propra-
nolol significantly greater than those observed for placebo.
Further research revealed that beneficial effects particularly emerged under condi-
tions of a stressor (J. K. Alexander et al., 2007). Individuals were asked to solve ana-
grams and compound remote associates either under conditions of stress (involving
public speaking and arithmetic tasks) or without stress (performing reading and
counting tasks) and either with placebo or propranolol. Stress impaired performance
on the measures of cognitive flexibility (compound remote associates and anagrams),
but cognitive flexibility was significantly improved under propranolol relative to pla-
cebo. Physiologic measures (e.g., heart rate) confirmed that the stress-inducing tasks
were associated with increased heart rate and that as expected propranolol reduced
heart rate in both the control and stress conditions. In contrast, neither a measure of
visuospatial memory (a complex figure task) nor a task assessing visual-motor coordi-
nation and processing speed (a grooved pegboard test) was affected either by stress or
by propranolol. Given this apparent specificity to measures of cognitive flexibility,
these researchers propose that their findings suggest that the noradrenergic system
may serve to modulate “the neural circuitry that may play a role in [. . .] creativity and
insight.” (J. K. Alexander et al., 2007, p. 475)
A double-blind within-subject study by H. L. Campbell et al. (2008) further under-
scores the moderating role of stress in determining the relation between beta-
adrenergic blockade and cognitive flexibility. These researchers found that a moderate
(40 mg) beta-adrenergic blockade was beneficial for particularly difficult anagram
tasks (defined as items that showed the lowest third of performance in the placebo
condition) and also for participants who, overall, found the tasks more difficult
(those who scored in the slowest third overall in response times). Neither weaker nor
stronger beta-adrenergic blockades (20 mg and 60 mg, respectively) yielded benefits
and, indeed, acted to impede performance on easy problems and for participants who
were already able to solve the problems. A broadly similar pattern of outcomes was
obtained for compound remote associate problems, and, intriguingly, for verbal
fluency tasks (letter fluency and category fluency) and also for visuospatial analogical
reasoning as assessed by Raven’s Progressive Matrices. In contrast, no effects were
found on a measure of set shifting, assessed with the Wisconsin Card Sorting Test
(WCST).
As suggested by H. L. Campbell and colleagues (2008) this difference in how the
different tasks were affected by beta-adrenergic blockade might reflect a difference
between “constrained flexibility,” involving shifting between a limited number of
options, as required by the WCST, and “unconstrained flexibility,” involving a search
through many different options, as required for the anagram, fluency, and remote
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 417
associates problems. However, it is also possible that the failure to observe effects on
the WCST reflected decreased power to detect effects because, given concerns about
test-retest effects, the WCST, unlike the other tasks, was administered on a between-
subjects rather than a within-subjects basis. In addition, and perhaps more impor-
tant, as we saw in Chapter 8, whereas the card-sorting task provides a measure
of reactive flexibility, requiring adaptability to changing external cues, the other
measures more strongly tap spontaneous flexibility.
Beversdorf et al. (1999, p. 2767) speculated that findings on the beneficial effects
of propranolol might also help to explain some instances of everyday insight.
Sometimes we repeatedly approach a difficult problem without success, but then the
solution arises as a sudden insight at a moment of rest, such as just before falling
asleep. These researchers speculate that “these moments of insight would therefore
occur when arousal and noradrenergic activation are known to be at their nadir.”
Indeed, postural effects—lying down rather than standing—themselves affect the
activity of the locus coeruleus-noradrenergic system, with decreased arousal levels
when lying down (Cole, 1989; Svensson, 1987). In line with the findings from studies
using pharmacological interventions described earlier, in an experimental explora-
tion, Lipnicki and Byrne (2005) found that healthy young adult participants solved
anagrams significantly more rapidly when they were supine than when they were
standing; in contrast, mental arithmetic solution rates were unaffected by posture.
The broad role of the noradrenergic system in enabling flexible adaptation to novel
circumstances will be further considered in the penultimate section of this chapter.
Volz and von Cramon (2006) attempted to differentiate intuition from both implicit
learning and insight. With regard to implicit learning, they noted,
Dane and Pratt (2007; also see Hodgkinson, Langan-Fox, & Sadler-Smith, 2008)
also argue for a distinction between insight and intuition, pointing to the further
difference that, in insight, one often becomes aware of the logical connections sup-
porting a particular solution or answer, whereas in intuition “one is unable to con-
sciously account for the rationale underlying the judgment that has arisen” (p. 40).
In seeking to delineate the possible brain correlates of intuitive processing, a
number of investigators have focused on the medial orbital frontal cortex as a possible
candidate. The medial orbital frontal cortex is crucial in enabling everyday decision
making and in guiding sound life judgments (e.g., Eslinger & Damasio, 1985) and has
also been found to be activated during hypothesis testing and guessing (Elliott, Dolan,
& Frith, 2000; Petrides et al., 2002). It is also a brain region that receives inputs from
all sensory modalities.
Bar et al. (2006) reported activity in medial orbital frontal cortex when partici-
pants initially guessed whether degraded visual stimuli (masked, or spatially filtered
grayscale photographs) that they were shown were common everyday objects or
abstract sculptures. Using the high temporal resolution provided through magnetoen-
cephalography (MEG), it was found that, in a comparison of successfully identified
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 419
50
40
30
20
10 lvf-RH
rvf-LH
0
1 2 7 15
Solving time
Together, these outcomes suggest that the right hemisphere advantage in solution-
related activation emerges over time, during a sustained effort to solve the problem.
These findings are in line with broader evidence that there are hemispheric differences
in the degree of focus or specificity of semantic activation. In particular, based on a
range of evidence involving hemispheric differences in language processing, research-
ers (e.g., Beeman, 1998; Beeman et al., 1994; Stringaris et al., 2006; see also Ben-Artzi,
Faust, & Moeller, 2009; Coulson & Wu, 2005) have proposed that the right hemi-
sphere engages in coarse semantic coding, such that it weakly and diffusely activates
large semantic fields representing various alternative meanings and more remote or
distant associations. In contrast, the left hemisphere is thought to engage in relatively
fine semantic coding, strongly focusing activation on small semantic fields represent-
ing either a single interpretation or on a few close and contextually appropriate
associations.
Although in many circumstances, the ability of the left hemisphere to quickly
narrow the focus of activation is advantageous—honing in on the correct interpreta-
tion and decreasing the accessibility of incorrect alternatives—there are times when
this narrowing may be disadvantageous, as when the solution that is focused on is
misleading, an unusual meaning is intended, or the intended meaning is less direct, as
in metaphors, or jokes, or inferences. In these circumstances, the diffuse activation
maintained in the right hemisphere could enable access to alternative interpretations
and thereby also facilitate reinterpretation of the linguistic discourse. The larger
422 BRAIN AND ENVIRONMENT
semantic fields of the right hemisphere might increase sensitivity to the overlap of
peripheral semantic features activated by various words in the language (or problem)
context, thereby helping to integrate and connect elements of the discourse (or
problem situation), and potentially helping with structure building, maintaining
coherence, and deriving the main themes or gist of the situation.
An important situation where the coarse coding of the right hemisphere might
prove helpful is in generating inferences. To take an example from Beeman et al.
(1994): If you hear that John walked near glass, you may recognize that glass can cut.
According to coarse semantic coding theory, this sort of information is more likely to
be activated, although only weakly, in the right than in the left hemisphere. If, later,
you also hear that John called out to the lifeguard for help then you might also
activate the information that one can call out for help for many different reasons, one
of which may be that one has injured oneself—including by being cut. This informa-
tion is, again, more likely to be activated in the right than in the left hemisphere. The
combined activation of foot, glass, and cry may summate to produce “cut.” Figure 9.6
schematically summarizes the proposed differences in the processing of the right
versus left hemispheres with regard to this example.
Extended to problem solving and insight problem solving in particular, the right
hemisphere coarse semantic coding theory:
predicts that, because insight problems misdirect solvers, the left hemi-
sphere will focus on interpretations that do not lead to solution, whereas the
right hemisphere maintains solution-related (as well as misdirected) activa-
tion. Coarse semantic coding also predicts that, because right hemisphere
solution activation is diffuse, it may be overshadowed by stronger more
focused activation in the left hemisphere, or may be too weak to be gener-
ated as a solution. However, when solution candidates are presented to prob-
lem solvers the right hemisphere activation can help in judging whether
those candidates are indeed solutions. […] That is, at the very least, right
hemisphere activation can be used to help recognize the solution if or when
it is encountered. It is also possible that, at some point, problem solvers
could use this activation to help generate solutions. (Beeman & Bowden,
2000, pp. 1238–1239)
12 inches 12 inches
heel
toes sock heel
toes sock
foot foot
CUT CUT
Figure 9.6. Coarse Versus Focal Semantic Coding. Illustration of coarse
versus focal semantic coding (upper row) and the effects of such coding on the
activation of distantly related words (lower row). According to coarse semantic coding
theory, encountering a word such as “foot” leads to differing patterns of activation in
the left versus the right cerebral hemispheres. The left hemisphere strongly activates a
smaller focal semantic field (upper row, on the left), whereas the right hemisphere
weakly activates a larger more extended semantic field (upper row, on the right). Thus,
in the situational inference context described in the text, whereas encountering the
word “foot” might not lead to the activation of the secondary meaning “12 inches” in
the left hemisphere, this secondary meaning might be activated in the right
hemisphere (upper row). In addition, the more focal semantic fields in the left
hemisphere do not overlap with the concept “cut,” whereas the larger semantic fields in
the right hemisphere do (lower row). If the weak but overlapping activations from
multiple sources summate, then an inferred concept that connects distantly related
words will be activated in the right hemisphere. Reprinted from Beeman, M. J.,
Friedman, R. B., Grafman, J., Perez, E., Diamond, S., & Lindsay, M. B. (1994, p. 29),
Summation priming and coarse semantic coding in the right hemisphere, Journal of
Cognitive Neuroscience, 6, 26–45, with permission from Copyright 1994, MIT.
right hemisphere. This region is recruited during language tasks that require the use
of distant semantic relations between words (Chiarello et al., 1990; Jung-Beeman,
2005), and both right and left anterior superior temporal gyri are involved in
language tasks such as understanding figurative language (e.g., Mashal et al., 2007),
extracting themes (St George et al., 1999), and generating the most appropriate
424 BRAIN AND ENVIRONMENT
endings to sentences (Kircher et al., 2001). Using fMRI, Jung-Beeman, Bowden, and
colleagues (2004) found that this region was more active during insight than for non-
insight solutions. In a converging study, using electrophysiological (EEG) recordings,
these investigators also found increased high-frequency (gamma-band) neural activity
in this same region directly before participants consciously realized the solutions to
compound remote associates problems—but only for those problems that were
self-reported as having been solved via insight, and not for problems reported to have
been solved via noninsight means.
These results suggest that the representation of the correct solution may be
activated at a subconscious level in the right hemisphere before insight actually occurs,
and, as suggested by Kounios and colleagues, raise the possibility that “analytic and
insight processing can occur in parallel” (Kounios et al., 2008; p. 282; also see Kounios,
1993). A more recent investigation of insight processing, using a series of different
riddles as the stimuli, also reported systematic insight-related changes in EEG activity
well before the moment of self-reported insight (Sheth, Sandkühler, & Bhattacharya,
2009). These researchers observed high-frequency (gamma) band activity for correct
responses (hits) compared to false-positive responses in right frontocentral brain
regions from between 8 and 1 seconds prior to participants’ reports of insight.
Additional findings suggest that our brain state immediately before we encounter
a particular problem may influence whether we are likely to solve the—not yet speci-
fied—upcoming problem using insight or by noninsight methods (compare with our
earlier discussion, in Chapter 8, in the section on “Task Switching,” of spontaneous
fluctuations in neural processing that were systematically related to subsequent mea-
sures of cognitive flexibility). Kounios and colleagues (2006) presented participants
the compound remote-associate problems during fMRI scanning under conditions
where there was a variable and unpredictable rest period prior to the presentation of
the problems (either 2, 4, 6, or 8 seconds). When they examined brain activity during
this preparatory interval (at which point the problem had not yet been presented),
they found that although many brain areas showed declining activity across the inter-
val (consistent with a return to baseline levels of activity), some regions consistently
showed increases in activity. Furthermore, this activity systematically varied accord-
ing to whether the upcoming problem was one that the participants self-reported as
having been solved by insight, or by noninsight methods.
One of the clearest increases of this form was shown in the anterior cingulate
cortex. Increased activity in the anterior cingulate during the preparatory interval was
associated with a significant increase in the likelihood that the following problem
would be solved by insight. The anterior cingulate cortex has repeatedly been associ-
ated with conflict monitoring, and it perhaps provides a signal regarding the need to
exert greater top-down cognitive control such as maintaining or switching one’s atten-
tion, or selecting a response from competing responses (e.g., Botvinick, Cohen, &
Carter, 2004; E. K. Miller & Cohen, 2001). But this poses a puzzle inasmuch as the
increased activity occurred when there was not yet a stimulus to which to respond or
indeed any apparent competing alternatives to adjudicate between.
Attempting to grapple with this puzzling pattern, Kounios et al. (2006) speculate
that the increased activity may have reflected the attempt to suppress irrelevant
thoughts (such as daydreaming or continued processing of the previous target) thereby
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 425
enabling the participant to approach the to-be-presented problem with a “clean slate.”
On this account, it might be proposed that insight problem solving, compared with
noninsight problem solving, is particularly vulnerable to interference from internally
generated, not immediately relevant thoughts. However, other accounts of the
increased brain activity in anterior cingulate are also possible. For example, as we saw
earlier in Chapter 8, in the section on “Task Switching,” Leber, Turk-Browne, and Chun
(2008) also found that the activity in anterior cingulate during a preparatory interval
was predictive of performance on the upcoming trial—but in this case the increased
activity was associated with increased flexibility in a task-switching paradigm, reflect-
ing improved task set reconfiguration on switch trials. These researchers further sug-
gested that such flexibility likely does not arise in response to the individual’s
evaluations of the recent task demands, and it may be something that individuals
cannot directly control, given that participants “largely are unable to adjust their
flexibility willfully, despite detailed feedback and motivational payoff schemes” (Leber,
Turk-Browne, & Chun, 2008, p. 13595).
A further possibility is suggested by a more recent fMRI study. Subramaniam,
Kounios, and colleagues (2009) found evidence that increased preparatory activity in
a more posterior and dorsal region of the anterior cingulate cortex prior to insight
solutions was reliably associated with increases in positive mood. These investigators
concluded that “positive mood is one factor that enhances activity” in this region and
that “this mediates the shift toward insight solutions” (Subramaniam et al., 2009,
p. 427). They further proposed that “positive mood enhances insight, at least in part,
by modulating attention and cognitive control mechanisms via the [anterior cingulate
cortex], perhaps enhancing sensitivity to detect non-prepotent solution candidates”
(Subramaniam et al., 2009, p. 415). Thus, the precise role of anterior cingulate activity
before trials that are associated with successful task reconfiguration and before
problems that are associated with successful insight-based problem solving remains
unclear. We return to this question in the subsequent section.
Additionally, it is important to keep in mind the particular types of problems that
were used in the study by Kounios and colleagues (2006), namely problems with which
the participants had no prior familiarity, with each remote associate problem being
discrete and unrelated to the others, and no clear way in which one could prepare
beforehand for the upcoming problem perhaps beyond being as “open” and attentively
focused as possible. The patterns of brain activity observed before successful “insight”
under these conditions might be quite different from those found for other sorts of
insight problems, particularly more complex and extended problems, to which an
individual might devote numerous hours of consciously directed, and also less deliber-
ate but still “goal-guided” thinking. For the latter sorts of problems, “preparatory
activity” in the form of attempted mastery and integration of related and background
material is essential; additionally, for these sorts of problems, at least sometimes, “not
immediately relevant” internally generated thoughts might instead comprise still-to-
be-articulated associative connections that would lead to solving the problem.
Nonetheless, recent findings examining electrophysiological measures recorded
during a different sort of more complex and sustained creative task have further
pointed to the importance of “screening out” irrelevant information during successful
divergent thinking. Grabner and colleagues (2007) examined event-related EEG
426 BRAIN AND ENVIRONMENT
were more likely to use incidentally presented peripheral cues to help them solve the
problems than were persons who were less proficient at this task. They attributed
these differences to “greater responsiveness to priming,” “a wider deployment of
attention” (Mendelsohn & Griswold, 1966, p. 430), and “less screening out of
‘irrelevant’ past experiences” (Mendelsohn & Griswold, 1964, p. 431) by individuals
who are highly creative during problem solving. Do such between person differences
in levels of creativity and the typical breadth of deployment of attention lead
to characteristic differences in brain activity, even during “unstructured” situations
in which there is no particular task to be undertaken? More specifically, does the
“neural context” of someone nominally at rest, or at least with no particular (exter-
nally determined) task at hand, systematically correlate with subsequent (not yet
encountered) problem solving approaches in ways that differ for, on the one hand,
someone who is prone to adopt an insightful, intuitive strategy towards problems
versus, on the other hand, someone who is inclined to take a systematic, analytically
based approach?
To examine whether brain activity during a resting phase might differentiate
between individuals who would tend to solve problems via insight versus more sys-
tematic search, Kounios et al. (2008) used high-density EEGs to record participants’
resting brain states. They recorded EEGs under two resting conditions (first with eyes
closed and then with eyes open) and then gave participants a series of anagrams to
solve. Crucially, participants were not aware at the time of the resting state measure-
ment that they later would be asked to solve problems. Additionally, and using a pro-
cedure also successfully adopted in previous work, during the subsequent
anagram-solving phase, participants were asked to indicate, for each anagram, how
they had solved each problem. They indicated whether they had solved each of the
anagrams through insight, involving an abrupt emergence of the solution into con-
sciousness, or through systematic search, involving a “methodical, conscious, search
of problem-state transformations” (Kounios et al., 2008, p. 281).
Overall about 70% of the anagrams were solved within the allotted time period (16
seconds), and slightly more than one-half (56%) of the problems were reported as
having been solved through insight. The ratio of problems that participants reported
as having solved by insight versus through systematic search was used to define two
groups (via a median-split procedure) with one group composed of participants who
predominantly solved the problems using insight (high insight group; insight to non-
insight ratio = 3.5) and the other composed of participants who used insight less fre-
quently (low insight group; ratio = 0.8). Importantly, the two groups did not differ in
their overall rate of anagram solutions, or their overall response times. However, con-
sistent with participants’ self-reported strategies, an analysis of the anagram error
rates revealed that there was a significant correlation between the tendency to solve
problems systematically and errors of commission, or the forwarding of proposed
solutions to the anagrams that were incorrect—perhaps reflecting guessing based on
partial information just before the allotted time per problem ran out. In contrast, the
tendency to report solving by insight was correlated with timeouts or errors of omis-
sion—perhaps reflecting a reluctance or inability to guess, even when time was run-
ning out, because partial information was not available or was not available to
conscious awareness (R. W. Smith & Kounios, 1996).
428 BRAIN AND ENVIRONMENT
in such undirected states will vary from moment to moment, and from individual to
individual, it has been broadly characterized as involving several forms of “spontane-
ous cognition,” including recollections of past events and anticipations and planning
for future events (e.g., Andreasen et al., 1995; Binder et al., 1999). Thoughts that are
about something other than the current task and the current environmental stimuli
(e.g., Singer & Antrobus, 1963; Singer & Schonbar, 1961), variously termed “stimulus
independent thoughts,” “task-unrelated thoughts,” “task-unrelated imagery and
thought” (e.g., Antrobus, 1968; Antrobus et al., 1966; Giambra, 1995), or “mind wan-
dering” (e.g., Smallwood & Schooler, 2006; Smallwood et al., 2009), tend to occur
during periods of low task demands, such as when performing a task that is highly
familiar and well practiced, or simple sensory tasks in which little attention is needed
for adequate performance (e.g., Greicius & Menon, 2004; McKiernan et al., 2003). Less
frequently, task-unrelated thoughts also emerge in high-demand contexts, such as
during a novel complex task requiring careful attention to the sequencing of steps (e.g.,
M. F. Mason et al., 2007; see also Antrobus, 1968; Killingsworth & Gilbert, 2010).
The default network that tends to be active during these undirected task states has
been characterized as “a brain system much like the motor system or the visual system”
that encompasses “a set of interacting brain areas that are tightly functionally
connected and distinct from other systems within the brain” (Buckner et al., 2008,
pp. 4–5). Very similar regions have been observed as showing greater activity in the
periods in between directed tasks in neuroimaging paradigms that involve compara-
tively longer phases of undirected activity on the order of minutes (“block” design
studies) and when the between-task phases are considerably briefer, on the order of
seconds and typically as little as 2–10 seconds (“event-related” studies). Across differ-
ent methodologies—including both block- and event-related task designs, as well as
functional connectivity analysis—a distributed set of regions has been found to be
more active in the between-task condition (e.g., Buckner et al., 2008; Greicius et al.,
2003. See also K. J. Miller, Weaver, & Ojemann, 2009 for recent support using direct
electrophysiological measurements and Greicius et al., 2009 for evidence from diffu-
sion tensor analyses.) These regions are in association cortex (not sensory or motor
cortex) and very consistently include medial prefrontal cortex, posterior cingulate
cortex/retrosplenial cortex, and the inferior parietal lobule. Additionally, each of the
methods has revealed activity in the hippocampal formation, and in lateral temporal
cortex, extending into the temporal pole, though these hippocampal and lateral
temporal cortical activations are comparatively more strongly apparent in the func-
tional connectivity analysis approach. Anatomical evidence suggests that these regions
comprise a series of subsystems, interconnected via both direct and indirect anatomic
projections, that converge on key “hubs” particularly in posterior cingulate cortex,
and that are connected with the medial temporal lobe memory system.
Several studies have shown that there are systematic relations between the control
of attention and activity in the default network. For instance, Weissman et al. (2006)
observed that on trials in which participants responded comparatively more slowly
during a demanding global/local selective-attention task—suggesting a lapse of atten-
tion to the task—activity in brain regions involved in regulating attention decreased
(e.g., in dorsal anterior cingulate and prefrontal cortex), but activity in regions of the
default network (e.g., posterior cingulate) increased.6 Another study (C. S. Li et al.,
430 BRAIN AND ENVIRONMENT
2007) that required speeded responding together with the inhibition of a strong
prepotent tendency to respond (on trials with a “stop signal” during a go/no-go task)
yielded a similar outcome. Trials on which participants failed to inhibit responding
(that is, stop errors) were preceded by increased default network activity (e.g., in bilat-
eral posterior cingulate). Stated differently, greater activity in these regions predicted
that a “stop error” would occur on the immediately upcoming trial.
In other work, increased activity in posterior cingulate cortex during an incidental
encoding task was found to predict that stimuli that were presented at that point
would subsequently prove to have been forgotten (Otten & Rugg, 2001). That is, in
contrast to increased brain activity in other regions such as left prefrontal and tempo-
ral cortices that have been shown to predict that particular stimuli would subsequently
be remembered (e.g., A. D. Wagner et al., 1998; see Paller & Wagner, 2002; A. D. Wagner,
Koutstaal, & Schacter, 1999, for review), greater activity in the default network was
predictive of which items would be forgotten (see Uncapher & Wagner, 2009, for review
and discussion). Using a different approach, Christoff and colleagues (2009) sporadi-
cally presented probes that asked participants to report, directly, if their mind had
“wandered” from the performance of a difficult but tedious sustained attention task.
Both participants’ reports of mind wandering and performance errors on the atten-
tion-demanding task were preceded (in the 10 seconds prior to the probe) by greater
activation in the default network, for example, in medial frontal and posterior cingu-
late cortex.
What functional roles does the default network play in human cognition? Several
differing accounts have been suggested. One account proposes that the default net-
work, or portions thereof such as posterior cingulate cortex (e.g., Gusnard & Raichle,
2001), is associated with an “exploratory state” (Shulman et al, 1997, p. 661), or of
“watchfulness” regarding the external environment (Gilbert, Simons et al., 2006,
p. 56; Gilbert et al., 2007). When in this externally watchful state, the individual is
thought to broadly, globally, and spontaneously scan the environment, such as in task
situations that do not require extensive processing of presented stimuli, or where
it is unclear where targets or relevant information may appear (e.g., Hahn et al., 2007).
A related account, forwarded particularly with regard to the role of medial rostral pre-
frontal cortex in this network, is the “gateway hypothesis” (e.g., Burgess, Dumontheil,
& Gilbert, 2007). According to the gateway hypothesis, activity in medial rostral pre-
frontal cortex is associated with situations that require the deliberate tuning of the
individual’s attentional bias: either toward current sensory input or toward internally
generated thought. It has been suggested that a process of deliberate biasing toward
external information would be especially beneficial for tasks associated with a high
level of automaticity, or very monotonous tasks that tend to be associated with
substantial numbers of stimulus-independent or task-unrelated thoughts yet also
require ongoing monitoring of the current environment. Support for the inter-
pretation that activity in medial prefrontal cortex might reflect such biased or prefer-
ential orienting toward the external environment has been provided by analyses of
participants’ response times. Greater activity in this region, on a trial-by-trial basis,
was associated with faster response times—not slower responses, as might be antici-
pated if participants were engaging in task-unrelated thoughts (e.g., Gilbert, Simons,
et al., 2006).
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 431
Another account focuses on the role of the default network in particularly self-
relevant cognition. This hypothesis has been concisely summarized by Buckner and
colleagues, who propose that “the fundamental function of the default network is to
facilitate flexible self-relevant mental explorations—simulations—that provide a
means to anticipate and evaluate upcoming events before they happen” (Buckner
et al., 2008, p. 2; Buckner & Carroll, 2007). Multiple sources of evidence, showing that
several apparently different sorts of activities often elicit activity in the default
network, have led to this account. Meta-analyses of the brain regions activated during
autobiographical memory retrieval have shown a marked correspondence between
those regions that are recruited during the recollection of self-related memories from
one’s past, and the regions that comprise the default network (e.g., Maguire, 2001;
Svoboda, McKinnon, & Levine, 2006). In addition, engaging in other complex tasks,
such as imagining events that may occur in the future (Addis & Schacter, 2008; Addis,
Wong, & Schacter, 2007; Suddendorf & Corballis, 1997, 2007), thinking about the
thoughts of others (Saxe & Kanwisher, 2003; Saxe & Powell, 2006), and reaching
decisions about how one should act in complex moral situations or dilemmas (e.g.,
J. D. Greene et al., 2001; B. J. Harrison et al., 2008) all also have been associated with
activity in this interconnected network. The largely common recruitment of the
default network across these surprisingly diverse tasks prompted the suggestion that
the default network is specifically involved in the simulation of perspectives that are
different from the present (e.g., Buckner & Carroll, 2007).
A recent quantitative meta-analysis, using activation likelihood estimation (ALE)
analyses to determine statistically significant concordance of activated voxels across
more than 75 studies, has similarly provided support for the proposal that there is a
common neural basis for a number of different processes, including autobiographical
memory, navigation, theory of mind (e.g., understanding the thoughts of other
people), and the “default mode” (Spreng, Mar, & Kim, 2009). These four domains
showed closely overlapping recruitment of medial parietal regions (posterior cingu-
late, precuneus, and retrosplenial cortex), medial prefrontal cortex/anterior cingulate
(including BA 10 and BA 32), left parahippocampus/hippocampus, as well as in left
lateral prefrontal cortex (inferior frontal gyrus, BA 47), and in the temporo-parietal
junction, extending posteriorly into a region in left occipital cortex.
Subdivisions of the default network, and predominant functions associated with
those subdivisions, have also been suggested. One subdivision may particularly draw
on contents from episodic memory. Based on a marked convergence of regions involved
in the default network and those recruited during successful episodic memory retrieval,
it has been proposed that a subsystem, involving the hippocampal formation, and also
the posterior cingulate cortex, inferior parietal lobe, and portions of the medial pre-
frontal cortex, may be especially involved in providing associations and relational
information from memory, and may perhaps be modulated in accordance with the
extent to which past episodic memory is relevant or useful to the task at hand.
For example, this subsystem may particularly contribute to the processes of “scene
construction.” As described by Maguire and colleagues, in scene construction, we
mentally generate and maintain complex and coherent scenes or events by retrieving
and integrating relevant information from modality-specific regions into a spatial
context that can then be manipulated and visualized (Hassabis, Kumaran, & Maguire,
432 BRAIN AND ENVIRONMENT
2007; Hassabis & Maguire, 2007). These investigators found that a core network of
regions was activated across several sorts of memory and imagination tasks. A similar
core network of regions was activated when individuals constructed new fictitious
scenes for the first time in the scanner (e.g., “lying on a sandy beach in a tropical bay”),
when they remembered recently imagined experiences from a prescan interview, and
when they remembered their own (“real”) personal experiences that had also recently
been recalled during a prescan interview. An extended network of brain regions,
involving left and right hippocampus, parahippocampal gyrus, retrosplenial cortex,
posterior parietal cortex, and ventromedial prefrontal cortex showed increased activ-
ity across these different sorts of tasks compared to control tasks involving similar
operations but with respect to isolated, acontextual objects (e.g., recalling an object
that was visually presented during the prescan interview).
A second subsystem involving particularly dorsal ventromedial prefrontal cortex
may be involved in self-relevant mental simulations or, more generally, in forms of
thinking that require one to conceive of others or other things or beings “as being
social, interactive, and emotive like oneself” (Buckner et al., 2008, p. 24; see also
Legrand & Ruby, 2009). To take one example, greater activity in dorsal ventromedial
prefrontal cortex was observed when participants were asked to make judgments
about fictitious people who were characterized as being similar to themselves than
when the people they were asked to imagine were painted as quite different from
themselves (J. P. Mitchell, Macrae, & Banaji, 2006). Increased activity was also
observed when participants made judgments regarding whether presented words
could describe the psychological state (e.g., curious, frightened) of a target entity
(either a person or a dog) than when they decided if the words could describe a physi-
cal part (e.g., artery, liver) of the target (J. P. Mitchell, Banaji, & Macrae, 2005; see J. P.
Mitchell, 2009, for review).
Considering findings from neuropsychology, Shamay-Tsoory and colleagues (2009)
have presented evidence suggesting that lesions to ventromedial prefrontal cortex
(BA 11 and BA 10) impair “cognitive empathy,” involving the tendency to spontane-
ously adopt the psychological point of view of others, and to imaginatively transpose
oneself into fictional situations. In contrast, lesions to the inferior frontal gyrus (BA
44) tended to impair “emotional empathy,” involving the individual’s feelings of
warmth, compassion, and concern for others, and a tendency to experience self-ori-
ented feelings of anxiety and discomfort in tense interpersonal situations. The latter
observations are perhaps consistent with the role of this or of nearby dorsal premotor
regions (see Cattaneo & Rizzolatti, 2009; Molenberghs, Cunnington, & Mattingley,
2009) in imitation, emotion recognition, and the early emotional matching/mirroring
of what has been termed the mirror neuron system (e.g., Rizzolatti, Fogassi, & Gallese,
2001; Zaki, Weber, Bolger, & Ochsner, 2009; however, see also Hickok, 2008, and
Mahon & Caramazza, 2005 for critical evaluation).
More generally, evidence from several apparently disparate forms of psychopathol-
ogy and mental disorders, including autism, schizophrenia, and also depression,
obsessional disorders, and other conditions, such as Alzheimer’s disease, has provided
further support for the notion that the default network is crucial to our ability to
engage in cognitive-perceptual-emotional simulations. These studies also underscore
the central functional importance of the interrelations between activity in the default
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 433
not aware (rather than aware) that their thoughts had strayed from the task at hand
suggests that the executive involvement might be in the service of the thoughts to
which they had wandered (e.g., current personal concerns and unresolved matters).
Although this activation pattern differs from the pattern of results observed
during many tasks and baseline conditions […], it is reminiscent of the
neural recruitment observed during creative thinking […], where executive
regions such as the dorsal [anterior cingulate cortex] and default network
regions such as the [posterior cingulate cortex] are activated before solving
problems with insight. Also, a similar parallel recruitment of executive
and default regions has also been observed during naturalistic film viewing
[…], which is related to immersive mental experience. […] Thus, mind
wandering may be part of a larger class of mental phenomena that
enable executive processes to occur without diminishing the potential
contribution of the default network for creative thought […] and mental
simulation […]. Although it may undermine our immediate goals, mind
wandering may enable the parallel operation of diverse brain areas in the
service of distal goals that extend beyond the current task. (Christoff et al.,
2009, p. 8723)
These results suggest that a simple dichotomy between activation of the default
network versus the executive control network will not adequately account for some of
the more intermediate and transitional modes involving both aspects of control (e.g.,
a focus on particular goals or problems) and aspects of noncontrol (e.g., spontaneous
thinking). Additionally, these findings raise the fundamental question of what brain
regions or network(s) of brain regions might assume a role in switching between the
central executive versus default networks.
Important recent work by Sridharan, Levitin, and Menon (2008) has begun to
address this question. Using several chronometric analyses techniques and causal con-
nectivity analyses to directly assess the temporal dynamics and causal interactions of
specific nodes within the central executive and default networks, these researchers
pointed to right frontoinsular cortex and dorsal anterior cingulate cortex as assuming
a key role in such switching. Although these two regions are often activated during
tasks that draw on central executive control, such as attention, working memory, and
response selection tasks, they also activate under a large number of other conditions,
such as in response to pain and uncertainty, and have been repeatedly implicated in
successful self-regulation in tasks involving meditation (see Tang et al., 2009, for
review and discussion).
Right frontoinsular and dorsal anterior cingulate cortex also appear to show
divergent patterns of intrinsic connectivity during resting states. Connectivity analy-
ses performed by Seeley and colleagues (2007) found different patterns of intrinsic
connectivity between these regions and other regions that are prominently activated
in central executive control tasks, such as bilateral dorsolateral prefrontal cortex and
lateral parietal cortices. In particular, right frontoinsular and dorsal anterior cingulate
cortex showed prominent intrinsic connectivity with other paralimbic regions, with
the limbic system, and with subcortical and brainstem structures, including regions
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 435
Additionally, VENs develop late both in ontogeny—in humans, they first appear in
very small numbers in the 35th week of gestation, and the newborn has only about
15% of the number of VENs found in the 4-year-old (Allman et al., 2005)—and also in
phylogeny, having been found only in humans, great apes, cetaceans, such as the
bottlenose dolphin and the beluga whale (Butti et al., 2009), and elephants (Hakeem
et al., 2009).
Intriguingly, the insula’s extremely diverse and virtually omnipresent role in a very
wide range of conditions involving awareness, has recently led to the proposal that
this region, based on the combination and integration of multiple forms of “saliency”
maps, is involved in the representation of the “now” that crucially contributes to a
sentient self. The insula is active not only in tasks requiring attention, cognitive
choices, and intentions but also in tasks involving “music, time perception and, unmis-
takably, awareness of sensations and movements, of visual and auditory percepts, of
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 437
the visual image of the self, of the reliability of sensory images and subjective expecta-
tions, and of the trustworthiness of other individuals” (Craig, 2009a, p. 65). Given
this ubiquitous involvement, Craig (2009a, p. 67) has proposed that representations
in the insula provide “a substrate for the sequential integration of homeostatic condi-
tions with the sensory environment and with motivational, hedonic and social condi-
tions represented in other parts of the brain,” and that “this substrate is constructed
on the foundation provided by the feelings from the body.”
In line with the general posterior-to-anterior processing gradient for increasing
abstraction in the frontal cortex (e.g., Amodio & Frith, 2006; Christoff, Keramatian
et al., 2009; see also Chapter 8), there is a posterior-to-anterior progression of repre-
sentations of saliency from the posterior to the anterior portions of insular cortex
(see the schematic diagram in Fig. 9.7). Whereas posterior insula represents more pri-
mary interoceptive states, intermediate (and incrementally more anterior) represen-
tations integrate successively “homeostatic, environmental, hedonic, motivational,
social and cognitive activity to produce a ‘global emotional moment’” that “represents
the sentient self at one moment of time.”
More speculatively, this framework can also be extended to account for the sense of
our selves in time (see Fig. 9.7, lower panel). As characterized by Craig (2009a, p. 67;
see also Craig, 2009b), anatomically “repeating” the fundamental unit of the represen-
tation of “the material me”—that is, the self at one moment in time—and somehow
indexing this to an endogenous time-base, could allow the generation of “a set of
repeated meta-representations of global emotional moments that extends across a
finite period of time.” Additionally, this “anatomical structure (a ‘meta-memory’)”
could provide “the basis for the continuity of subjective emotional awareness in a finite
present”—with additional storage buffers or “workspace” (e.g., Kranczioch et al., 2005)
for the individual global emotional moments allowing the process of comparing past,
present, and future feelings, and enabling the instantiation of a “reflexive observer.”
Other investigators, for example, Allman and colleagues (2005) have suggested
that “VENs may relay a fast intuitive assessment of complex social situations to allow
the rapid adjustment of behavior in quickly changing social situations” (Watson et al.,
2006, p. 1112. See also W. J. Kuo et al., 2009, for evidence of selective recruitment of
the insula and anterior cingulate cortex in a co-ordination game eliciting rapid intui-
tive assessments of what is likely to be salient to another person.) Similarly, it has
been suggested that “the VENs and related insular circuitry may be involved in moni-
toring changes in the physiological network of the individual’s own body and that
individual’s social network” and may assume an important role in “initiating homeo-
static corrections to changes in network states” (Hakeem et al., 2009, p. 247). These
approaches7 thus share a common emphasis on how ongoing representations of our
current internal and external state in the frontal insular cortex and anterior cingulate
(a) Posterior insula Anterior insula
Present
Past
438
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 439
the sentient self at one moment of time.” The upper portion of (b) illustrates how “a
series of global emotional moments can produce a cinemascopic ‘image’ of the sentient
self across time,” whereas the bottom portion illustrates how “the proposed model can
produce a subjective dilation of time during a period of high emotional salience, when
global emotional moments are rapidly ‘filled up’”. ACC, anterior cingulate cortex;
DLPFC, dorsolateral prefrontal cortex; VMPFC, ventromedial prefrontal cortex.
Reprinted from Craig, A. D. (2009a, p. 67), How do you feel—now? The anterior insula
and human awareness, Nature Reviews Neuroscience, 10, 59–70, with permission from
Macmillan Publishers Ltd. Copyright 2009, Macmillan Publishers Ltd.
440 BRAIN AND ENVIRONMENT
cortex activity were inversely coupled during the successful intentional regulation of
negative affect in response to the stimuli.
Investigations with depressed individuals also have shown that depressed persons
demonstrate greater sensitivity to misleading negative feedback than do controls. It
has been proposed that disrupted top-down control by the prefrontal cortex of the
amygdala may underlie this hypersensitivity to negative feedback (Tavares et al.,
2008). Recent work has also shown that individuals who were formerly depressed, but
who are fully recovered, demonstrate greater activation in the amygdala and less acti-
vation in the dorsolateral prefrontal cortex and in the anterior cingulate cortex than
do controls when they are presented with critical comments from a family member.
These observations suggest that “vulnerability to depression may be characterized by
abnormalities in nodes along cortico-limbic pathways that can be revealed by certain
types of affective challenges” (Hooley et al., 2009, p. 117; also cf. Way et al., 2010).
There is considerable and growing evidence that the neurotransmitter serotonin
may be involved in enabling resilience to aversive events, and also in the failure of
resilience that can lead to clinically severe states of depression in the face of adverse
life events (Deakin, 1991; see also the discussion of the possible contribution of sero-
tonergic dysfunction to the lack of cognitive flexibility observed in conditions such as
depression in the section on “Set Shifting and Reversal Learning” of the previous
chapter). Individuals who are depressed show reduced circulating plasma tryptophan,
an essential amino acid that is a precursor of serotonin. Depressed individuals who are
taking medications that are selective serotonin reuptake inhibitors and who are then
challenged with dietary tryptophan depletion have been found to show a depressive
relapse that then again resolves after replenishment of tryptophan levels through a
return to regular food intake (e.g., P. L. Delgado, 2006; P. L. Delgado et al., 1990). It has
been proposed that the serotonergic system that originates in the median raphe
nucleus in the brain stem and projects to the hippocampus and associated areas of the
cortex, functions as an adaptive system during times of chronic stress (Deakin, 1991;
Deakin & Graeff, 1991; Graeff et al., 1996). When this system breaks down, tolerance
to chronic stress is impaired and leads to depression in humans and symptoms of
learned helplessness in animal models.
Most studies using the technique of dietary tryptophan depletion have not found
that healthy controls respond to the depletion with depressive mood changes. However,
such changes have been reported in individuals who are vulnerable to depression,
including those with a family history of depression and those with genetic markers of
vulnerability (Neumeister et al., 2002). Based on theoretical notions of the role of
“learned helplessness” (e.g., Seligman, 1972) and of uncontrollable adverse events in
contributing to the onset of depression, Richell et al. (2005) combined dietary trypto-
phan depletion with manipulations of uncontrollable noise stress (possibly inducing a
situational sort of learned helplessness) or controllable noise stress (not likely to lead
to learned helplessness). Normal individuals who were jointly challenged with trypto-
phan depletion and uncontrollable noise showed a significant increase in negative
mood compared with when they were exposed to controllable noise stress. These
researchers found significant or near-significant interactions of type of stress (control-
lable vs. uncontrollable) on mood analog scales tapping depression-dejection and help-
lessness; the depletion manipulation combined with uncontrollable noise also led to a
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 441
significant and selective increase in reported sadness. Together, these results are con-
sistent with an important role of the serotonergic system in mediating resilient
responses to stress but also highlight the importance of the nature of the stressors
(controllable vs. uncontrollable).
Two important contributors to resilience may be positive affectivity (the “trait of
being joyful, interested, and contented in life,” Yehuda et al., 2006, p. 384) and opti-
mism (which also contributes to positive affect). For example, as we saw earlier in
Chapter 7, optimism is positively related to successful adaptive coping (Linley &
Joseph, 2004) and to psychological adjustment during life transitions and medical
challenges such as coronary artery bypass surgery (Brissette, Scheier, & Carver, 2002;
Scheier et al., 1999). People in general tend to show a modestly overpositive or slightly
“too optimistic” view of their likely experiences, overestimating the likelihood or
nature of positive future events in regard to themselves, and underestimating nega-
tive characteristics or events (e.g., Lench & Ditto, 2008; S. E. Taylor & Brown, 1988;
Weinstein, 1980).
In a double-blind placebo-controlled study comparing the effects of acute trypto-
phan depletion and acute stress exposure on individuals with, versus without, a family
history of depression, Firk and Markus (2008) found that stress led to less positive
affective bias. These effects tended to be stronger in those with a family history of
depression. Cools and colleagues (2008) suggested that the typical observation that
healthy individuals show greater accuracy in predicting rewards than in predicting pun-
ishments or aversive events may reflect resilience to aversive signals: “Resilience pro-
tects subjects from the detrimental consequences of exposure to adversity and enables
them to quickly recover from negative experiences” (Cools et al., 2008, p. 2297).
Using a rat model to investigate the effects of a controllable stressor versus an
uncontrollable stressor on behavior and neurochemical function, Amat and colleagues
(2005) presented evidence to suggest that medial prefrontal cortex may be particu-
larly important in learning the contingencies that are operative in a given situation—that
is, precisely what the animal can do to control the stressor or to avoid it. Aversive and
stressful events elicit quite different behavioral, emotional-motivational, and other
consequences depending on whether the source of the stress is under behavioral con-
trol, such that the animal or person has the ability to alter the onset, offset, duration,
or intensity of the adverse conditions through behavioral actions. Uncontrollable
stressors lead to changes in behavior that resemble depression and anxiety and acti-
vate serotonergic neurons in the dorsal raphe nucleus much more strongly than do
controllable stressors, leading to sensitization of these neurons.
Amat et al. (2005) examined learning and behavior in rats that could terminate
painful shocks (through wheel-turning) or could not do so (uncontrollable condition).
In the uncontrollable condition, the duration of the shocks was determined by a
“yoked” animal in the controllable condition, thereby equating the duration and
timing of the shocks the two groups received. (Yoking is a procedure whereby the
reinforcement events, such as shocks or food pellets, administered to one animal in an
experimental condition are also given, in the same frequency and order, to an animal
in the “yoked” control condition. However, whereas the reinforcement events in the
experimental condition are consequences of the animal’s own behavior, for the yoked
control they are given entirely independently of the animal’s behavior.) In addition,
442 BRAIN AND ENVIRONMENT
for each group of animals, the researchers either injected an inert vehicle into the
medial prefrontal cortex or injected the drug muscimol that would interfere with
medial prefrontal function. They found that inactivation of ventral medial prefrontal
cortex eliminated the stressor resistance that is usually observed when animals have
behavioral control, such that the controllable stressor now elicited outcomes as though
it was uncontrollable (e.g., exaggerated fear, failure to learn, and activation of the
serotonergic dorsal raphe nucleus).
These results suggest that, if a stressor is controllable, then the ventral medial
prefrontal cortex inhibits the stress-induced activation of the dorsal raphe nucleus, so
that the behavioral consequences of uncontrollable stress are not observed. Stated
differently, these findings suggest that “the presence of control inhibits stress-induced
neural activity in brainstem nuclei, in contrast to the prevalent view that such activity
is induced by a lack of control” (Amat et al., 2005, p. 365). More broadly, these out-
comes imply that:
Highly aversive events are likely to drive limbic and brainstem structures that
induce negative affective and motivational experiences; control, perceived con-
trol, or more generally, the ability to cope may activate [ventral medial prefron-
tal] inhibition of these limbic and brainstem processes. From an evolutionary
perspective, it may be sensible that activation of “lower” centers by strongly
aversive events came first, and that as species developed the ability to cope
with such events by behavioral means, inhibition from “higher” centers under
conditions of behavioral coping then developed. (Amat et al., 2005, p. 369)
the stressor” (Amat et al., 2008, p. 1184). Allowing an animal to have behavioral control
can reduce the consequences of exposure to significant stress but other factors—such
as the provision of “safety signals” indicating when the stressors will end—also can
have beneficial effects on subsequent learning and adaptive responding.
Ongoing current experiences and activities, such as regular physical exercise, may
also bolster resilience and resistance to learned helplessness (e.g., Greenwood & Fleshner,
2008; also see Chapters 10 and 11). In humans, regular physical activity, including either
aerobic exercise or resistance training, is well documented to reduce the incidence of
stress-related mood disorders, such as depression and anxiety (e.g., Stathopoulou et al.,
2006; Wipfli et al., 2008). Beneficial effects of voluntary exercise (wheel running) have
also been shown in rats. For example, four or more weeks of voluntary wheel running
reduced animal behaviors that may reflect anhedonia, or diminished experience of plea-
sure, elicited in response to chronic unpredictable stress, such as reduced preference for
sweetness (Zheng et al., 2006). Rats that were allowed to engage in voluntary wheel run-
ning for a period of 6 weeks before being exposed to a learned helplessness manipula-
tion (exposure to a series of uncontrollable tail shocks) were resistant to the behavioral
deficits that uncontrollability usually elicits, such as deficits in escape learning and exag-
gerated fear. These “protective effects” of voluntary exercise depended on the duration
of the prior regular exercise—if less than 3 weeks they were not observed, but they were
apparent after 6 weeks (Greenwood et al., 2005). Notably, these duration differences
also correspond with the timeframe in which attenuation of stress-induced activity of
dorsal raphe nucleus serotonergic neurons is observed, with such attenuation observed
after 6 weeks but not after only 3 weeks of wheel running.
Other work from this lab (Greenwood & Fleshner, 2008) demonstrates that volun-
tary exercise was especially protective against stress-induced deficits in escape learn-
ing only when the stressor and the testing environments differed from one another.
This suggests that exercise reduced the extent to which “learned helplessness” general-
ized to other contexts, but it did not disrupt context-relevant conditioned fear learning.
Indeed, in the original context, exercised rats actually showed more freezing than did
sedentary animals, but this difference disappeared if there was no reexposure to the
stressor, and the animals were allowed to continue voluntary exercise for several
weeks. In combination, these findings indicate increased flexibly adaptive responding
in the exercised rats: They demonstrated strong fear-relevant behavior when the
specific testing environment warranted such behavior, but did not excessively general-
ize that learning to other contexts, and also adaptively “unlearned” the fear-relevant
behavior in the testing environment when conditions changed.
The beneficial effects of exercise in reducing responses to uncontrollable stressors
also are likely to be mediated through the effects of exercise on the serotonergic
system and on norephinephrine. For instance, several weeks of voluntary wheel run-
ning led to decreased elevations of a serotonin metabolite in the hippocampus and
amygdala following uncontrollable foot shock (Dishman et al., 1997), pointing to
decreased serotonergic activity and reduced release of serotonin during exposure to
the stressor in the regularly exercising animals. In contrast, compared to sedentary
rats, the shortened escape latency for rats that were allowed to engage in wheel run-
ning was associated with increased concentrations of norephinephrine in the locus
coeruleus and the dorsal raphe nucleus.
444 BRAIN AND ENVIRONMENT
Ongoing research that is seeking to determine the sites of the neuroplasticity that
leads to these beneficial exercise-induced effects on resilience to stress is focused on
three possible mechanisms: the dorsal raphe nucleus (through a gradual increase in an
inhibitory serotonin autoreceptor, 5-HTIA, over a period of 6 weeks or so), the locus
coeruleus (through constrained activation of norepinephrine neurons during uncon-
trollable stressors, reducing the drive from the locus coeruleus to the dorsal raphe
nucleus), and the ventral medial prefrontal cortex (through facilitated inhibition of
serotonergic neurons in the dorsal raphe nucleus). Although, to date, there is little
direct evidence for a role of exercise in facilitating medial prefrontal cortical function
specifically, several converging findings are broadly consistent with this as a possible
mechanism. For instance, as further developed in Chapters 10 and 11, there is consid-
erable empirical support for the view that, in humans, exercise improves executive
control functions involving the prefrontal cortex (e.g., Colcombe & Kramer, 2003),
and exercise has been shown to lead to increased volume in prefrontal regions
(Colcombe et al., 2006).
Evidence from animal research work also suggests that the ability of medial
prefrontal cortex to modulate responding to stressors may be substantially shaped by
early life experiences, such as maternal separation. Whereas repeatedly separating rat
pups from their mother for prolonged periods during the postnatal period increases
their vulnerability to stressors later in life, brief separations combined with human
handling appear to make the animals later more resilient to stressors than are pups
that are left undisturbed. These conditions are also associated with behavioral differ-
ences (e.g., the handled rats may show less anxiety) and neurochemical differences in
the stress responses shown by the animals. For instance, relative to early experiences
with brief handling, early maternal separation leads to enhanced hypothalamic corti-
cotropin-releasing factor expression and increased release of adrenocorticotropin and
corticosterone in response to stressors (Francis et al., 2002; Plotsky et al., 2005).
These effects may be partially compensated for (but not entirely reversed) through
enriched environmental stimulation at the time of weaning (Francis et al., 2002).
Using in vivo electrophysiology to record unit and local field potentials in bilateral
medial prefrontal cortex in response to a pharmacological stressor, Stevenson et al.
(2008) found that rats that had been exposed to maternal separation showed attenu-
ated basal unit activity in this region, particularly in the right medial prefrontal cortex.
In contrast, the pharmacological stressor selectively activated right medial prefrontal
cortex neurons in the handled animals. Early maternal separation also altered the
functional relations between left versus right medial prefrontal cortex, such that
hemispheric coupling was attenuated by early maternal separation but was increased
by early handling.
Although these results are still preliminary, and await replication and extension,
they clearly converge with other evidence, reviewed earlier, concerning the important
role of medial prefrontal cortex in resilient responding to stress. Additionally, the dif-
ferences in hemispheric lateralization and synchronization of medial prefrontal cortex
in this animal model are consistent with other evidence from both animal studies
and studies with humans suggesting that the right hemisphere plays a preferential
role in mediating adaptive coping responses to stressors (e.g., Sullivan & Gratton,
1999; Thiel & Schwarting, 2001; Tomarken, Davidson, & Henriques, 1990).
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 445
CS– and vice versa), then these cells rapidly altered their responding to reflect the new
contingencies, thus tracking their activity with the current target “meaning” rather
than the target’s stimulus properties (Aston-Jones et al., 1994; see also the section on
“Reversal Learning” in Chapter 8).
A further source of evidence for the important role of locus coeruleus neurons in
within-task changes that require rapid behavioral adjustment by the organism is
provided by the results of a rather different experimental paradigm that involved
odor discrimination in rats. In the experiment, the presentation of a stimulus (a light)
signaled the beginning of an experimental odor discrimination trial and thereby also
signaled an opportunity to gain reward. If the signal occurred at a point in time when
the animals were disengaged from the experimental paradigm, the signal elicited rapid
and consistent responding of locus coeruleus neurons (shown in 46 out of 49 record-
ings, with an average latency of 155 ms, and SD of 1.8 ms), concurrent with the
animals’ reengagement on the task as shown by the animals orienting to the light, and
then moving to and actively sniffing the odor port at which the discrimination trials
were presented (Bouret & Sara, 2004). If there was no longer any reward for the
task (extinction trials) then the animals no longer oriented to the light, and the locus
coeruleus neuron activity also was not observed; however, such activity again reemerged
if the contingencies changed and trials were again reinforced. Activity of single units in
the locus coeruleus also rapidly changes as a function of the novelty of a stimulus in
freely moving rats as they explore an environment (Vankov et al., 1995).
Taking into consideration the anatomical distribution of noradrenergic terminals,
and these diverse forms of rapidly adaptive responding by locus coeruleus neurons,
Bouret and Sara (2005) proposed that the noradrenaline signal has a general “reset
function” and can facilitate changes in widespread networks in the forebrain that are
involved in specific cognitive functions:
A schematic depiction of the way in which functional brain networks might be rap-
idly modulated by locus coeruleus activation and noradrenaline release, thereby facili-
tating cognitive and behavioral flexibility, suggested by these authors is presented in
Figure 9.8. An initial behavioral state might be represented in a particular pattern of
neurons such as that shown in Phase 1 of the figure, with some neurons active (shown
in black) and part of the current network, and others not active (shown in gray) and
not part of the network. It is proposed that when a stimulus is presented that induces
a cognitive shift, then activation of the locus coeruleus occurs directly before the
behavioral shift; the widespread activation of the locus coeruleus allows it to simulta-
neously influence multiple target structures, and so promote widespread modification
of the networks and their interactions. As shown in Figure 9.8, these modifications in
the networks may include both the new engagement of some cells (symbolized by
arrows) and new disengagement (symbolized by crosses or x’s) of other cells. Expanding
on some of these notions, Doya (2008) observed that “The optimal setting of the
448 BRAIN AND ENVIRONMENT
LC activation
Noradrenaline
release
Shifting
stimulus
learning rate depends on how quickly the world is changing. [. . .] After an abrupt
change of the environment, it is more appropriate to totally reset what has been
learned (or switch to another learning module) and start over. Norephinephrine is
implicated in such ‘resets’ of ongoing activities” (Doya, 2008, p. 414).
In their early demonstration of locus coeruleus responses during a continuous
vigilance task in the monkey, Aston-Jones et al. (1994, p. 4477) suggested that the
timing of the impulses recorded in the locus coeruleus (about 200 ms) was such that
the impulses evoked by target cues “would be expected to reach the cerebral cortex at
about the time that certain cortical slow-wave activity is generated, in particular, P3
(similar to P300) waves.” This suggestion presages several more recent studies explor-
ing the relation between this electrophysiological component and various forms of
novelty detection versus responsiveness to task-related rule changes in humans.
One such study contrasted the effects on the P3a component elicited by feedback
during a modified version of the Wisconsin Card Sorting Task, and that elicited
by truly novel events in an “oddball” task (the P3a is an anteriorly oriented P3
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 449
component). Barceló et al. (2002) found that feedback signaling that the current
sorting rule for the card sorting task had changed, and that thus directed the partici-
pant’s mental set to new task rules, elicited P3a responses that were similar to those
elicited by nontarget novel events in an oddball task in their amplitude, latency, and
scalp topography. Even though the feedback used to signal that a new sorting rule was
now in effect (a tone) was not itself novel, and even though participants had both
learned that the tone denoted a rule shift, and had been exposed to the tone on a
number of earlier rule shift occasions, nonetheless it elicited a P3a response. Given
that “the ‘shift’ tone prompted the subject to think differently, and to flexibly adopt a
new solution (i.e., a new task set) for the same card sorting problem” these outcomes
argue that “a common brain response system may be responsible for processing
both stimulus and task novelty” (Barceló et al., 2002, p. 1890).
In subsequent work, Barceló et al. (2006) reported a similar outcome. In this study,
it was additionally found that the amplitude of novelty P3 activity that was elicited
varied with the amount of informational uncertainty arising with the switch signal.
There was a larger P3 response when the task required switching from one rule to one
of two other rules (three-task condition) than when the task required switching
from one rule to another rule (two-task condition). Thus, these investigators argued
that the P3a response should be “understood more broadly as signaling the call of an
executive control system to ‘think differently’ (i.e., to shift mental set)” (Chong et al.,
2008, p. 121).
Electrophysiological findings on the effects of frontal lobe lesions on responses to
novelty are likewise in line with this account. Comparing patients with frontal lobe
lesions to controls who were matched on age, education, estimated intelligence quo-
tient, and mood, Daffner and colleagues (2000) found that the individuals with fron-
tal lobe damage showed a markedly reduced amplitude in the P3 response to novel
stimuli, and also showed reduced duration of viewing novel stimuli. In contrast, there
was little difference in P3 amplitude between the frontal lesion and control group for
target stimuli. Furthermore, the magnitude of the P3 amplitude attenuation effect to
the novel stimuli in the individuals with frontal lesions was correlated with measures
of apathy and with viewing duration in response to the novel stimuli but not to target
stimuli. These authors argued that these results suggest that:
Finally, there is recent evidence suggesting that the P3/P3a response may be
modulated by contextual factors that shape how individuals will interpret novel or
potentially deviant or unusual stimuli. Based on the results of what, as we will see, was
450 BRAIN AND ENVIRONMENT
itself a novel approach to the study of novelty, Chong and colleagues were led to
conclude that the P3a may “index decisions about the extent to which potentially
significant or deviant events merit the allocation of additional processing resources”
(Chong et al., 2008, p. 121).
Although under many conditions, the processing of novelty can be detrimental—if
it distracts from ongoing task performance—under other circumstances, positive
engagement with novelty may be beneficial, stimulating cognitive-emotional process-
ing and interest and (as will be clearly developed in the next two chapters) helping to
sustain and extend one’s cognitive capabilities and mental agility. Yet much of the
evidence relating to the role of the P3 in the processing of novelty has been obtained
under conditions in which individuals had little control over the presentation of the stim-
uli, and where the interpretation of novel (“oddball”) events was that of distracters
from the experimentally designated “target task.”
To examine the effects of how participants were likely to interpret novel stimuli—
as unwelcome potential distracters versus inviting inducements to exploration—on
the physiological correlates of novelty responding, Chong et al. (2008) manipulated
the task instructions that they gave to participants during a picture-viewing task.
Whereas participants in the target-focused condition were informed that the purpose
of the experiment was to see how well people respond to targets when they are exposed
to a variety of distracter images, those in the curiosity-focused condition were told that
the purpose of the experiment was to learn how curious people are about things in
their environment. Participants were also told that they could view each picture for as
long as they liked, advancing to the next stimulus by pressing a key. The stimuli shown
to participants were of three types: a repetitive standard stimulus (a right-side-up
triangle, shown on 70% of the trials), a target stimulus (an upside-down triangle,
shown on 15% of the trials, to which participants were asked to make a foot-press
response), and unusual and unfamiliar line drawings, such as impossible or frag-
mented objects (shown on 15% of the trials).
The viewing time data showed that the two groups did not differ in how long they
spent viewing the repetitive standard stimulus, with both groups looking at it only
briefly (approximately 1 second). In contrast, the two groups markedly diverged in
how long they looked at the novel stimuli. On average, the curiosity-focused group
looked at the novel stimuli for over 10 seconds, whereas the target-focused group
accorded them only about 1 second.
Surprisingly, in the target-focused condition, there also was no difference in the
magnitude of the P3 response to novel stimuli versus to the standards (or in viewing
duration or a later positive slow wave component)—apparently contrary to well-
established novelty “oddball” paradigm results, which regularly demonstrate a greater
P3 response to novel trials. Critically, such paradigms typically provide participants
with little direct control of the onset of the trials. In the current “subject-controlled”
paradigm, participants were able to determine the onset of trials. As suggested by
Chong et al. (2008), this increase in control may have facilitated greater top-down
modulation of the responses to novel stimuli, enabling individuals to allocate their
attention more closely in correspondence with the experimental context and enabling
stronger modulation of how novelty is processed. “Although novelty detection was
automatic under both conditions, additional processing was strongly modulated by
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 451
the experimental context established by the task instructions” (p. 131). Participants
in the target-oriented condition, in which novel events served as distracters, limited
the degree of processing allocated to those events, but participants in the curiosity-
focused condition extended the time and resources allocated to those events. (Note
that these outcomes pertain particularly to the P3 component; in contrast, in both the
study of Chong et al., 2008, and in more recent work by Tarbi et al., 2011, using a
modified version of the ignore vs. explore paradigm, an earlier and more perceptually-
based component, the anterior N2, that appears to be largely automatic, was not influ-
enced by task relevance, and still signaled perceptual novelty regardless of whether
novelty was to be attended or to be ignored; see Tarbi et al., 2011, for discussion.)
These results, based on adopting a methodology that places more of the situational
task context within the control of the participant, demonstrate the close intersections
of individually initiated goal-related deliberate processing and more automatic stimu-
lus-driven processes. The more abstract global orientation that participants adopted
regarding novel stimuli either substantially extended—or truncated—the amount of
processing allocated to novel events, and also altered whether those events were very
rapidly classified as “odd” enough to elicit the P3 electrophysiological signature of an
“attention-evoking” event. “Novelty,” then, is not a dimension that can be defined
entirely without reference to the mental set that an individual has adopted toward
events that are new, and whether situational constraints are such as to encourage,
versus to discourage, our self-initiated deeper exploration of what is new.
analyses demonstrated that whereas neither the BAS nor frontal asymmetry
predicted BIS, BIS scores were significantly predicted by the magnitude of the No-Go
N2 effect and by ERN amplitude; in addition, BAS scores were predicted only by fron-
tal asymmetry. Thus, whereas higher BIS was uniquely associated with larger No-Go
N2 and ERN amplitudes that are linked with conflict-related processing in the anterior
cingulate cortex, higher BAS was uniquely associated with greater left-sided frontal
cortical asymmetry, consistently associated with approach orientation (e.g., Pizzagalli
et al., 2005).
Interpreting the association of higher BIS scores with the two ERP components,
Amodio and colleagues (2008) note that the “inhibition” indexed by these components
is likely a form of “bottom-up” inhibition. They propose that the N2 and ERN compo-
nents likely reflect “an initial bottom-up alerting to a response-relevant cue that is
associated with a slowing or stopping of ongoing action” (p. 17) that may, however, be
followed by an intentional, and top-down controlled withholding of a response, per-
haps relying on the BAS. These results thus converge with the concepts of undercon-
trol versus overcontrol, discussed in Chapter 5, particularly the question of whether
and when individuals might be, or seem to be, “too controlled”—showing what J. H.
Block and Block (1980, p. 43) characterized as an excessive “containment of impulses,
delay of gratification, inhibition of action and affect, and insulation from environmen-
tal distractors” that might then impede spontaneous adaptability. Carver (2005) sug-
gested that excessive BIS activity might itself comprise an automatic reactive form of
inhibition, rather than deliberate and top-down regulation of behavior:
C. Effortful control
[cortical, executive]
(inhibits an emerging impulse, and/or
fosters a nonemergent action)
Even if that does not happen, the emergent impulses may (or may not) be
restrained by an effortful (cortical) system that deliberates and chooses
among actions [shown in C]. The effortful system can also foster the emer-
gence of an action that is not strongly motivated at the reactive, impulse level.
The gray arrow indicates the possibility […] that avoidance impulses can also
emerge directly from the threat-sensitive subcortical system, which may (or
may not) be restrained by the effortful system. (Carver, 2005, p. 320)
Other research has attempted to relate either an individual’s BIS/BAS scores, or the
degree of electrophysiological frontal asymmetry that they demonstrate, to differences
in their responsiveness to particular sorts of rewards (Locke & Braver, 2008; Pizzagalli
et al., 2005). For example, testing healthy adults, Pizzagalli and colleagues (2005) found
that higher left-frontal baseline activity recorded in one experimental session was asso-
ciated with greater responsiveness to a reward condition in a later experimental ses-
sion. In the second session, participants were given different payoffs for accurately
performing a verbal recognition task. In some blocks of trials the contingencies were
neutral (feedback was provided, but correct and incorrect responses had no monetary
consequences), in others they were rewarding ($0.10 awarded for each correctly identi-
fied target), and in still others they were punishing ($0.10 lost, from an initial credit of
$2.50, for each missed target). Using a distributed source-localization technique to
examine the electrophysiological data, these researchers were able to demonstrate that
higher left-lateralized baseline activity, associated with a stronger reward bias, was
associated with distinct regions in the dorsolateral and in ventromedial prefrontal
456 BRAIN AND ENVIRONMENT
cortex. In addition, this baseline asymmetry was reliably predictive of the extent to
which participants were differentially responsive to the reward contingencies (com-
pared to the neutral contingencies), and it remained uniquely predictive of reward
responsiveness even after controlling for momentary (state) and longer term (trait)
differences in positive affect. These findings suggest that individual differences in pre-
frontal cortical resting asymmetry are associated “with a propensity to show approach-
related behavioral tendencies in response to specific cues” (Pizzagalli et al., 2005,
p. 811), perhaps also reflecting “stronger reinforcement representations” (p. 812).
Similar reward responsiveness and a positive correlation with higher BAS scores have
been found in a task involving a direct measure of cognitive control. Locke and Braver
(2008) found that, compared with a baseline condition, reward incentive (25 cents for
each trial faster than the participant’s median RT for responding during the baseline
blocks) led to reliably faster responses during a demanding cognitive control task: the
AX continuous performance task. In this task, participants are instructed to respond to
some trials (AX trials, in which the letter “A” is shown as a context cue at the beginning
of the delay period, and the letter “X” is shown later in the same trial, comprising
approximately 70% of all trials) but not to other trials (AY, BX, or BY trials, each occur-
ring on about 10% of the trials). The speed-up in response time in the reward blocks
(participants responded about 25% faster than they did without the reward incentive)
was not accompanied by a greater number of errors—except for to the AY trials.
The selective increase in error rates to the latter type of trials likely reflects
an increased use of a “proactive control strategy” in which participants proactively
maintained the context cue in mind to help them choose the right response when the
probe was presented. Given the probabilities of trials, such proactive control typically
leads to high levels of accuracy on the BX trials (the cue letter, B, predicts the correct
response of “nontarget” 100% of the time), and also on the AX trials (the cue letter, A,
predicts the correct response of “target” 87.5% of the time). However, proactively
maintaining the context cue leads to an increased likelihood of errors on the AY trials
because these are comparatively infrequent trials, and the context cue for these trials
is misleading (most often “A” is followed by X, requiring a “target” response, but in this
case it is followed by Y, and so requires a nontarget response).
Notably, when Locke and Braver (2008) examined regions that were positively
correlated with the rate of rewards that participants were able to earn during the
reward block, they found that reward rate significantly correlated with sustained
activity in frontopolar cortex. In addition, scores on the Behavioral Activating System
subscale from the BIS/BAS (Carver & White, 1994), designed to evaluate an individu-
al’s reactivity to cues related to reward, correlated with activity in right frontopolar
cortex (as well as with other reward-related processing regions, such as the orbital
frontal cortex, and the caudate nucleus). The posited bases of this positive correlation
between frontopolar cortical activity and increased motivation-induced performance
enhancement are somewhat speculative. However, one possibility is that the correla-
tion derives from individual differences in goal-related processing, perhaps reflecting
the comparatively more successful participants’ increased attention to relevant sub-
goals within the task or to the overall (relatively abstract) goal of maximizing the
amount of rewards earned.
These findings thus return us, conceptually, to the critical role of prefrontal cortical
regions in representing goals—where we began at the outset of Chapter 8—but
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 457
further provide the promise of jointly taking into account diverse contributions to
behavioral control, including also motivational and emotional contributors. Indeed,
although cognitive control and emotional/motivational states most often have been
considered separately, there is growing evidence that, at least under some conditions,
cognitive control and emotional/motivational states (such as approach/avoidance)
may form an “integrated” cognitive-emotional system. For instance, working memory
may be especially central for maintaining active goals, but emotion/motivation may
help to modulate those goals depending on changing circumstances, giving priority to
either approach or avoidance goals in a context-appropriate manner. According to
this account, formulated by J. R. Gray, Braver, and Raichle (2002), approach- versus
withdrawal-related motivational states are associated with different modes of infor-
mation processing, which then can alter the efficiency of specific cognitive functions:
Gray, Braver, and Raichle (2002) argued that a formal test for the integration of
emotion and cognition (or of any two psychological processes) requires “evidence that
neural activity in a single brain region is influenced by two processes (e.g., by emotion
and by cognitive control) but the influence of one process is ambiguous unless the other
is taken into account” (J. R. Gray, 2004, p. 46). Elaborating on this idea, Gray notes:
Initial behavioral evidence for such integration was provided by three experiments
(J. R. Gray, 2001) in which individuals were encouraged to be either in an approach-
related state (amusement) via watching comedy videos (e.g., excerpts from Candid
Camera) or a withdrawal-related state (anxiety) through watching horror videos
458 BRAIN AND ENVIRONMENT
(e.g., excerpt from the film Scream). After this emotion induction, participants were
asked to perform a working-memory task (a two-back task) involving either verbal
stimuli (requiring them to remember individual letters shown in a box on the screen)
or spatial stimuli (requiring that they remember the location of the boxes on the
screen). The rationale for considering working-memory for these two types of content
derived from known lateralization differences, with left frontal cortex particularly
involved in the active maintenance of verbal information but right frontal regions
especially important in the maintenance of spatial information (e.g., D’Esposito et al.,
1998; E. E. Smith & Jonides, 1999). If emotion influences cognitive control, then the
induction of an approach-related state, associated with left-lateralized frontal activity,
would be expected to facilitate performance on the left-lateralized verbal working
memory task, whereas induction of an avoidance-related state might adversely affect
this same task. In contrast, induction of a withdrawal-related state, associated with
relatively greater right-lateralized activity, might facilitate spatial working memory
performance but not verbal working memory performance.
Precisely this general pattern was found, particularly for participants who made
more errors than average across conditions: Whereas the approach-related state
enhanced verbal working memory, it impaired spatial working memory and whereas
the avoidance-related state enhanced spatial working memory performance, it inter-
fered with verbal working memory. In addition, this interaction was further associated
with individual’s self-reported approach versus withdrawal dispositions, as assessed by
the BIS/BAS questionnaire. Individuals who scored high on BIS (and low on BAS)
showed the interaction most strongly when exposed to the withdrawal/horror movie
manipulation, but those who scored high on BAS (and low on BIS) showed the interac-
tion most strongly when exposed to the approach/comedy show manipulation.
These initial behavioral findings guided the development of an fMRI study to exam-
ine whether, as predicted, both lateralized effects of emotion and cognition separately,
and also emotion-cognition integration, would be found within lateral prefrontal cortex.
Rather than a two-back working memory task, the researchers used a more demand-
ing three-back task, and rather than contrasting performance for letter versus spatial
content, they contrasted working memory performance for words (nouns) versus
faces (unfamiliar people). In addition, they included a neutral emotion condition
(watching a documentary) as well as the approach-related (comedy) and avoidance-
related (horror film) inductions.
The results showed that, as hypothesized, there was a bilateral region in lateral
prefrontal cortex (BA 9) that showed a crossover pattern of activation depending on
both the content of the working memory task and the emotion induction condition.
Although the direction of the modulation was such that there was less activity for
words in left lateral prefrontal cortex in the pleasant induction, and more for faces
(and the reverse for right lateral prefrontal cortex), a systematic crossover indicated
integrated processing, with the “match” between emotional state and task (e.g.,
approach-related induction + verbal content for the left; avoidance-related induction
+ visual content for the right) perhaps leading to a lower “load” and thus reduced
activity compared with the “mismatching” emotional state and task conditions.
A more extensive investigation, combining measures of personality, fluid intelligence,
and brain activation patterns during a working memory task (J. R. Gray, Burgess,
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 459
et al., 2005) provided further evidence for the conjoint influences of motivational and
cognitive contributors to working memory performance.
One final example—chosen as providing strong evidence that the influence of
personality-motivational factors on cognitive responding may further be modulated
by the degree of attentional specificity with which individuals can approach a task
(Most et al., 2006). In this fMRI study, participants were asked to examine a rapidly
presented series of pictures, in order to identify a target. The target was either
described in specific terms (e.g., look for a building rotated 90 degrees to the right or
left) or in nonspecific terms (e.g., look for a building or a landscape that is rotated 90
degrees). Participants sometimes searched for a specific target, and at other times for
a nonspecific target, and the series of pictures included both neutral distractor images
and emotionally negative distractors (e.g., a man about to stab a woman). Participants
also completed a personality subscale that evaluated their harm avoidance tendencies.
Individuals who score low on this subscale tend to demonstrate relatively confident
temperaments; they also tend to engage in risk-taking behavior and to quickly recover
from stress. In contrast, high scorers on the measure tend to have anxious and tense
temperaments, to show risk avoidance, and to show slower recovery from stress.
Several brain regions were more active when participants maintained a specific
rather than a nonspecific attentional set, including bilateral middle frontal gyri, left
inferior frontal gyrus, and the left inferior parietal lobule. More important, the extent
of activation observed in the amygdala in response to the emotion-related stimuli
depended on the combination of the attentional set instructions and the participant’s
harm avoidance score. Whereas under the nonspecific attentional set, individuals with
high harm avoidance scores showed greater amygdala activity than did those with low
harm avoidance scores, when participants had a more specific target to look for, then
there was no significant difference in amygdala activity in relation to harm avoidance.
Stated differently, both high- and low-harm avoidant individuals were able to effec-
tively ignore emotional distractors when they could adopt a specific instructional set,
but high harm-avoidant individuals were unable to “screen out” the distractors when
they had only the nonspecific attentional guidance.
Furthermore, the increased “screening out” by the high harm-avoidant individuals
was correlated with increased activity in the anterior portion of anterior cingulate
cortex—such that participants who were high in harm avoidance showed increased
activity in this region to emotion-related stimuli only under the specific instructions.
Thus, the more focused instructions appeared to particularly bolster the cognitive- or
affective- monitoring capability of the harm-avoidant participants, and this was
shown both by less “automatic” responsiveness to the negative emotional stimuli,
manifested in reduced amygdala activity under the specific attentional set, and by
increased “controlled” responsiveness during the presentation of those otherwise
attention-grabbing emotional stimuli, as shown by increased anterior cingulate
cortical activity under the specific attentional set.
This study, then, like the investigations by J. R. Gray (2001) and J. R. Gray, Burgess,
and colleagues (2005), clearly demonstrates the “intimate interaction” that may
emerge between cognitive control and emotion. It thus provides further support for
the characterization of the domains of emotion and cognition (as well as motivation/
action and perception) as somewhat discrete, but also to some extent overlapping,
460 BRAIN AND ENVIRONMENT
with boundaries that, under particular task and other situational contexts, are perme-
able to one another. The schematic characterization of the iCASA framework, pre-
sented in Figure 1.2 in Chapter 1, reflects these and other findings (see also Barrett,
2009; Pessoa & Adolphs, 2010).
Looking Back
We have now concluded our “paired chapter” overview of some of the key findings—
from cognitive neuroscience and neuropsychology—relating to how “mental agility,”
in its many diverse forms, may be realized in the brain. We have considered the
possible brain bases of forms of reactive flexibility, such as set shifting and reversal
learning, and of spontaneous flexibility, essential to promoting effective and creative
responding in many fluency and divergent thinking tasks. We have also considered
neural contributors to several tasks that require adaptive movements between levels
of representational specificity and levels of control, ranging from visuospatial and
verbal analogies, to gist-based intuitive processing, to how we may access remote
associates to enable appropriate inferences and “insightful” restructuring of problem
contexts. The often critical role of emotion, and of motivation and goals, has been
underscored, as well as sometimes surprising intersections between these. To take
one example, we considered evidence that one’s orientation to stimuli, emphasizing
exploratory curiosity toward novel pictures or treating them as potential distractors
from the “main task” at hand, may either lead to the elicitation of the P3—one of the
electrophysiological “signatures” of novelty—or essentially eradicate that signature;
in contrast, such changes in task set left untouched an earlier and more perceptually-
based and bottom-up automatic signature of novelty, the N2.
Findings relating to cognitive flexibility not only from investigations at the brain
systems level but also at the level of single neurons and the neurochemical level have
received some attention, together with several findings from neuropsychology.
Prominent here is the pivotal evidence provided by the temporal variant of frontotem-
poral dementia (semantic dementia) in helping to establish “where” concepts are rep-
resented in the brain, and of the frontal variant of this same progressive disorder in
pointing to the central role of prefrontal cortex in evaluating and integrating multiple
relations in analogical and other forms of complex reasoning.
We have seen that even a comparatively simple task, such as remembering the first
of three presented stimuli for a short time, involves the dynamic coordination of
widely distributed brain regions in frontal, parietal, medial-temporal, and occipital
lobes. Representation of a stimulus across a brief temporal period and intervening
stimuli is reliant on both active neuronal firing in regions such as prefrontal cortex
and memory supported by short-term synaptic changes. Additionally, we have seen
that, although many investigative efforts have examined the brain systems and neural
connectivity that enables appropriate and flexible responding to experimentally and
externally determined stimuli and task contexts, a full understanding of how we
adeptly (or not so adeptly) respond to such tasks must take into account the activity
and connectivity of the mind/brain when there are few external demands—and our
thoughts are guided by internally generated goals and preoccupations, spontaneous
B ra i n B a s es of Level s of S pecificity and Lev e l s of C on t rol , Part 2 461
memories, and imaginative and deliberatively planful forays into the future. The grow-
ing evidence for the diverse contributions of the “default mode” network to multiple
forms of cognition may provide a healthy corrective to an overly narrow concentration
on experimentally and externally determined task conditions, encouraging investiga-
tive efforts to more fully recognize the cognitive, behavioral, and neural significance of
more spontaneous and internally generated activity, both during task performance
itself (for instance, in mind wandering, or other forms of concurrent task unrelated
thinking), and as a potentially potent sculptor of the “representational and processing
landscape” into which as yet not presented tasks and stimuli will need to make their
way. From the perspective of the iCASA framework, this bodes well for arriving at an
increasingly deep and connected understanding of both varying levels of representa-
tional specificity and varying levels of representational control—including not only
extremely controlled and highly automatic modes of processing but also more sponta-
neous and impromptu and intermixed modes.
10
Making Brain Paths to Agile
Thinking, Part 1
Correlational and Longitudinal Evidence
462
Making Br ain Paths to Agil e T h in k in g , Part 1 463
P L A S T I C I T Y O F C O R T I C A L M A P S I N R E S P O N S E TO
A LT E R AT I O N S I N S E N S O R Y - M OTO R I N P U T: B R A I N
C H A N G E S L I N K E D TO F U N C T I O N A L B E H AV I O R A L C H A N G E S
Changes in human brain activity arising as a consequence of changes in sensory-motor
input have been demonstrated using multiple methods. Clear alterations in the
cortical maps, relating to the cortical regions that “code for” or represent sensory
and motor information of an arm or hand, have been observed in persons who have
experienced restricted sensory-motor input to a limb following amputation of the
limb (e.g., Flor et al., 1995; Ramachandran & Hirstein, 1998). In normal individuals,
464 BRAIN AND ENVIRONMENT
the representation of the hand in the sensory cortical map of the body (sometimes
referred to as the Penfield map or sensory homunculus) is flanked on one side by the
sensory cortical representation of the face and on the other side by the upper arm,
chest, and shoulders. Using the functional brain imaging technique of magnetoen-
cephalography (MEG), Flor and colleagues (1995) showed that amputation of an upper
limb was associated with significant alterations in the somatosensory maps of the
persons affected. Specifically, sensory input from the face and from the upper arm had
“invaded” the somatosensory cortical region that previously—before the amputa-
tion—had represented the hand.
This suggests that nearby representations had “claimed” the region that otherwise
(before amputation) would have coded for sensory inputs from the hand
(Ramachandran, Stewart, & Rogers-Ramachandran, 1992a, 1992b). As Ramachandran
and Hirstein (1998, p. 1609) note, these early findings demonstrated that “the famous
Penfield map in [primary sensory cortex] that every medical student and psychology
undergraduate learns about, can be reorganized over a distance of at least 2 or 3 cm
even in the adult brain.”
Other researchers studying human sensory-motor representations, using brain-
imaging techniques such as functional magnetic resonance imaging (fMRI), have dem-
onstrated that there is increased cortical representation associated with the acquisition
of special motor skills. For instance, blind individuals who read Braille show an
increased cortical representation of the reading finger (Sterr et al., 1998). These indi-
viduals also may show recruitment of formerly “visual” areas of the occipital cortex
(V1 and V2) for tactile information processing (R. H. Hamilton & Pascual-Leone,
1998; see Driver & Noesselt, 2008, for broader discussion of causal interplay between
different senses). Similarly, in musicians who are string players compared to nonmusi-
cian controls, neuroimaging has shown an enlargement of the cortical somatosensory
representation of the digits of the left hand, used for the dexterity-demanding finger-
ing of the strings (Elbert, Pantev, Wienbruch, Rockstroh, & Taub, 1995).
Nonetheless, fascinating though they seem, such changes in the brain and neural
representations do not, on their own, tell us about the functional or cognitive-behavioral
significance (if any) of the changes. We might well ask, “What does a larger cortical
somatosensory representation of the digits on one’s hand really mean, functionally?”
In isolation from attempts to systematically relate apparent plasticity of neural
representations and of neural systems to relevant changes in actual behaviors and/or
sensory-cognitive function, these various forms of evidence are suggestive only.
However, a number of studies also have started to provide a more detailed picture of
the functional importance of such changes.
These studies suggest that there may be rapid, task-specific dynamic changes in the
cortical organization of several prestabilized maps that depend on experience in a
given domain. For example, Braun, Schweizer, et al. (2000) trained participants, over
a 4-week period, in 1-hour sessions each day, in a simultaneous sensory stimulation
task involving the thumb and little finger of one hand They also recorded high-resolu-
tion electroencephalographic (EEG) activity in participants at pretraining, during the
initial week of training, and post training. After training, there was greater segrega-
tion of the primary somatosensory cortical representation of these two digits than
before training—but this separation was apparent only when stimulus discrimination
Making Br ain Paths to Agil e T h in k in g , Part 1 465
was required, and not during passive stimulus perception for which stimulus discrim-
ination was not required. These results suggest that “different task-specific maps
evolve during the training period, which may then be activated selectively and dynam-
ically on demand” (Braun et al., 2001, p. 2260).
Braun and colleagues (2001) also have shown that the cortical representations of
the thumb and little finger show changes during a highly learned habitual movement—
that of handwriting. The cortical representations of these two digits were more distant
from one another during writing (with either hand) than during rest. Given these find-
ings with a well-learned task, the authors propose that “somatosensory cortex switches
between different, concurrently pre-existing maps depending on actual requirements”
and that such task-dependent activation of preexisting maps “might be a powerful
mechanism to optimize stimulus processing” (Braun et al., 2001, p. 2259).
Using fMRI in conjunction with psychophysical testing, Pleger and colleagues (2003)
demonstrated that tactile coactivation of adjacent receptive fields of the right index
finger led to increased spatial discrimination in the coactivated region. Stimulation was
applied to the finger using a small (8 mm) electromechanical device, called a solenoid,
for a period of 3 hours. This coactivation of the receptive fields representing the skin
portion underneath the solenoid led to an enhanced ability of participants to differenti-
ate between pairs of tactile stimuli that were applied to nearby locations on the finger.
These researchers further showed that enlargement of cortical territory in primary
somatosensory cortex (S1), assessed by fMRI, was linearly correlated with a lowering of
spatial two-point discrimination thresholds of the participants in the coactivated
region, such that participants were better able to differentiate between two nearby
points of stimulation following the period of tactile coactivation. Discrimination sensi-
tivity was not increased in a control condition involving much more focal stimulation
(single-site stimulation of only 0.5 mm on the left index finger) that did not lead to
coactivation of adjacent receptive fields. In addition, the increased two-point discrimi-
nation sensitivity in the coactivated region (mean = 1.28 mm, SD = 0.25 mm) resulting
from this brief intervention was temporary: After 24 hours, discrimination between
two points in the previously coactivated region (mean = 1.55 mm, SD = 0.26 mm) was
equivalent to that prior to the intervention (mean = 1.58, SD = 0.20).
Figure 10.1 shows, for an individual participant, the change in the cortical repre-
sentation of the right index finger that was observed, and also the corresponding psy-
chophysical changes in the same participant’s ability to differentiate between any two
points applied to the finger. Comparison of the pre- versus poststimulation brain
images shows an increased extent of activation in the somatosensory cortex; the pre-
versus poststimulation psychophysical curves show a shift of 0.14 mm in the separa-
tion distance needed for the participant to detect separate points of stimulation.
There is also increasing evidence that the recruitment of formerly “visual” areas of
cortex during tactile (Braille) reading in persons who are blind plays an important
functional role in Braille reading. These sources of evidence include (a) findings show-
ing that temporarily disrupting cortical function in occipital cortex—through the use
of transcranial magnetic stimulation (TMS)—disrupts Braille reading in early blind
subjects (L. G. Cohen et al., 1997, 1999); (b) neuropsychological evidence, involving
an early blind individual who experienced a bilateral occipital ischemic stroke, after
which she was no longer able to read Braille, yet other forms of tactile processing were
A B 120
Figure 10.1. Single subject Illustration of Changes in Functional Brain Activity and Psychophysical Sensitivity Arising
from the Coactivation of Adjacent Receptive Fields of the Right Index Finger. Panel (A) shows functional magnetic resonance
imaging (fMRI) BOLD signal detected in primary (S1) and secondary (S2) somatosensory cortex during the preexperimental phase, immediately
after the coactivation experimental phase, and 24 hours later, with activations projected on an axial (left), sagital (middle), and coronal (right)
T1-weighted, normalized MRI slice. Compared with the preexperimental assessment, following the stimulation phase, there was increased
contralateral activation in both primary and secondary somatosensory cortex; this increase in activation was no longer apparent 24 hours later. This
participant, and several others, also demonstrated slight increases in the ipsilateral secondary somatosensory cortex, but these ipsilateral
activations did not reach significance in the group-level analysis. Panel (B) shows the two-point discrimination threshold for the same subject
shown in (A), for the corresponding phases (preexperimental, immediately after the coactivation phase, and 24 hours later). Correct responses in
percent (red squares) are plotted as a function of the separation distance between the two stimulating tip points, together with the results of a
logistic regression line (blue with blue diamonds); the horizontal line indicates the 50% level of correct responses. After coactivation the
psychometric function showed a shift (by 0.14 mm) toward lower separation distances (compare the downward arrows for the upper and middle
graphs); this change in discrimination threshold also was no longer observed 24 hours later (compare the downward arrows across the three
graphs). Reprinted from Pleger, B., Foerster, A. F., Ragert, P., Dinse, H. R., Schwenkreis, P., Malin, J. P., Nicolas, V., & Tegenthoff, M. (2003, p. 647),
Functional imaging of perceptual learning in human primary and secondary somatosensory cortex, Neuron, 40, 643–653, with permission from
Elsevier. Copyright 2003, Elsevier. Note: See the insert for a full-color version of this image.
468 BRAIN AND ENVIRONMENT
unchanged (R. Hamilton et al., 2000); and (c) neuroimaging findings indicating
that neural activity in visual cortex (pericalcarine cortex) during Braille reading shows
laterality effects, differing for left- versus right-hand Braille readers, implying “specific
early processing of tactile information from the reading hand” (H. Burton et al., 2002,
p. 600). Other findings showing that, within individual Braille readers, the patterns of
activation in visual cortex are highly localized, also are congruent with a functionally
significant role. As argued by Burton and colleagues:
B R A I N C H A N G E S W I T H OT H E R F O R M S O F
LONG-TERM COMPLEX EXPERIENTIAL INPUT
Other brain imaging findings have pointed to additional plastic changes in the brain
in relation to experience. For example, it is known from research on food-storing bird
species that the size of the brain structures needed for spatial memory and navigation
(especially the hippocampus) can be influenced by behavioral demands. Food-storing
bird species, such as the black-capped chickadee, create food caches in diverse places
in the environment and then rely on an accurate and detailed spatial memory in order
to later recover their caches. In the black-capped chickadee, variations in the intensity
of food-storing activity are correlated with the size of the hippocampus (e.g., Smulders,
Sasson, & DeVoogd, 1995). Might a similar modification in the demands placed on
human brains for navigation lead to structural changes in the hippocampus—likewise
known to be critical for spatial memory and spatial navigation?
To address this question, researchers turned to a group of professionals who
regularly demonstrate high levels of complex spatial navigation: London taxi drivers
(Maguire et al., 2000). Taxi drivers in London must undertake extensive training,
typically lasting 2 years, to learn how to navigate between thousands of places in the
Making Br ain Paths to Agil e T h in k in g , Part 1 469
city, including the layout of 25,000 streets; they also must pass stringent examina-
tions by the Public Carriage Office before they can be licensed to operate (Woollett,
Spiers, & Maguire, 2009). Maguire and colleagues recruited 16 licensed London taxi
drivers, all of who had been taxi drivers for more than 1.5 years (mean time as taxi
driver = 14.3 years, range = 1.5 to 42 years). The drivers ranged in age between 32 and
62 years (mean = 44 years), and all took part in MRI scanning that allowed detailed
imaging of the structure of their brain.
Analyses of the brain images were then performed using the technique of voxel-
based morphometry. This is a method for comprehensively examining the whole brain
for changes in anatomical structure across groups of participants (e.g., Ashburner &
Friston, 2000). The technique was used to identify regions of brain gray matter con-
centration that differed significantly between the taxi drivers and a group of 50 healthy
males of approximately the same ages who did not drive taxis.
The analyses showed that, compared to the control participants, the taxi drivers
had significantly increased gray matter volume in the posterior hippocampus, on both
the right and the left. By contrast, the control participants showed greater volume in
the anterior hippocampus. In addition, the amount of time that the drivers had spent
driving taxis—both during training and after becoming qualified—was significantly
correlated with the volume of the right posterior hippocampus; right posterior gray
matter volume increased and anterior volume decreased with more navigation experi-
ence (Maguire et al., 2006). Greater volume in the midposterior hippocampus of taxi
drivers was also observed when taxi drivers were compared to a control group of
London bus drivers. The latter group likewise regularly navigated the city, but along a
constrained and much more limited set of routes. The finding that bus drivers did not
show similar changes in midposterior hippocampal volume helps to rule out several
other possible factors that might be postulated as contributing to the observed
plasticity, such as high levels of self-motion or increased stress, which may have char-
acterized both the bus drivers and the taxi drivers (Maguire et al., 2006).
Maguire and colleagues concluded from these findings that “the professional depen-
dence on navigational skills in licensed London taxi drivers is associated with a relative
redistribution of gray matter in the hippocampus” (Maguire et al., 2000, p. 4402). They
further argued that the significant positive correlation between right posterior
hippocampal volume and years of taxi-driving experience strongly suggests that the
differences were acquired through the greater demands on, and use of, navigational
knowledge, rather than preceding that experience. These results thus pointed to the pos-
sibility that there is “local plasticity in the structure of the healthy adult human brain as
a function of increasing exposure to an environmental stimulus” (Maguire et al., 2000,
p. 4402; see also Maguire, Spiers, Good, Hartley, Frackowiak, & Burgess, 2003).
The exact nature of the changes induced through such extensive development and
use of navigational knowledge, at a microscopic rather than macroscopic level, remains
unknown. Although the differential changes in the posterior versus anterior
hippocampus may reflect different mechanisms, it is possible that the changes are
interconnected, perhaps reflecting an “overall internal reorganization of hippocampal
circuitry” (Maguire et al., 2000, p. 4402). Research with aging rats has demonstrated
morphological alterations in the hippocampus that were correlated with the magni-
tude of spatial impairment shown by individual animals. Age-related decreases in the
470 BRAIN AND ENVIRONMENT
conceptual pause to delineate three key concepts that have emerged from research on
the effects of cognitive, social, and physical lifestyles on cognitive and brain function.
The three interrelated concepts are the notions of brain or cerebral reserve (sometimes
referred to as “passive” reserve), cognitive reserve (also sometimes referred to as
“active” reserve), and compensation.
the initial emergence of functional impairment, and, second, that less brain reserve
capacity acts as a vulnerability factor, such that a person with less brain reserve
capacity is at greater risk for functional impairment should a brain lesion occur.4
More recently, Y. Stern (2002) differentiated between passive models of reserve,
involving brain or neuronal reserve, versus active models involving, instead, cognitive
reserve capacity. In passive models, reserve is defined in terms of “the amount of
damage that can be sustained before reaching a threshold for clinical expression,”
whereas in active models, the focus is on “differences in how the task is processed.”
Although the distinction between passive and active models is not a strict dichotomy,
and the models are not mutually exclusive, passive models can be distinguished in
that they assume that there is some fixed cutoff or threshold (e.g., for Alzheimer’s
disease, something akin to the number of synapses available), after which functional
impairments will emerge for everyone. In addition passive models are essentially
quantitative models:
They assume that a specific type of brain damage will have the same effect in
each person, and that repeated instances of brain damage sum together.
Individuals differ only in their overall brain capacity, and brain damage is
either sufficient or insufficient to deplete [brain reserve capacity] to some
critical level. The model does not account for individual differences in how
the brain processes cognitive or functional tasks in the face of the disruption
caused by brain damage. It also does not address potential qualitative differ-
ences between different types of brain damage. (Y. Stern, 2002, p. 450)
There is considerable evidence to support the threshold model, yet, taken on its
own, it is not sufficient to account for all of the findings that have been reported (e.g.,
Staff et al., 2004). Most notably, qualitative differences in cognitive or active reserve,
involving an “ability to optimize or maximize performance through differential recruit-
ment of brain networks” (Y. Stern, 2002, p. 451) and perhaps reflecting the use of alter-
nate cognitive strategies may also be important. Thus, on the cognitive reserve account,
whereas one individual with Alzheimer’s disease may begin to express clinical features
of the disease after (for example) the loss of a given number of synapses, another
person who has greater cognitive reserve may still be able to function effectively with
the same number of synapses. This account argues that at least some of the effects of
education and occupational attainment do not necessarily reflect changes in gross brain
neuroanatomy linked to such attainments but may arise because individuals have
learned to process information in a more efficient manner. In the apt contrast proposed
by Stern (2002, p. 451), “The threshold approach supposes that the person with more
[brain reserve capacity] has more to lose before they reach some clinical cut-point. The
cognitive reserve hypothesis focuses less on what is lost and more on what is left.”
From this conceptualization, an important implication of the cognitive reserve
concept is that it should also apply to healthy individuals:
Since the changes in brain recruitment associated with reserve are a normal
response to increased task demands, this definition suggests that cognitive
reserve is present in both healthy individuals and those with brain damage,
and is reflected in the modulation of the same brain networks. In essence, an
Making Br ain Paths to Agil e T h in k in g , Part 1 473
Some initial support for this proposal was provided by Stern, Hilton, and colleagues
(2003) and also by Stern, Zarahn, et al. (2008), using fMRI with healthy individuals to
examine correlations between measures of cognitive reserve (e.g., Vocabulary) and
patterns of brain activity during different tasks that varied both in content and level
of difficulty. For example, Stern, Zarahn, et al. (2008) using a technique known as
canonical variates analysis, found that in younger but not older participants there was
a spatial pattern or brain network that modulated activity as a function of task load.
As task load increased—during both a verbal and an object working memory task—
this network became increasingly correlated with measures of cognitive reserve
(assessed both by Vocabulary and an estimate of intelligence based on the National
Adult Reading Test, or NART). The researchers speculated that “this spatial pattern
could represent a general neural instantiation of [cognitive reserve] that is affected by
the aging process” (Y. Stern, Zarahn, et al., 2008, p. 959).
Although emphasizing that functional interpretation of the brain areas of the gen-
eral network must be made cautiously—because the relation of cognitive reserve per-
tains to the entire spatial pattern—these researchers nonetheless remarked that many
of the regions that emerged have previously been observed in studies of controlled
processing, such as task switching and working memory (e.g., Braver et al., 2003;
Wager et al., 2004), and also that similar regions emerged in their earlier (Y. Stern
et al., 2003) study. Thus, “these consistent findings across studies and tasks provide a
preliminary suggestion that control processes may be an important component of
some aspects of [cognitive reserve]” (Y. Stern, Zarahn, et al., 2008, p. 966). Additional
support for these postulates could be provided by examining yet a still larger set of
tasks to determine whether a similar pattern emerges across additional task and stim-
ulus variations or, more ambitiously, by prospective studies. In the latter case, expres-
sion of the network would be first assessed in younger participants who then would be
followed across time, with the prediction that “higher expression will predict slower
progression of age-related cognitive changes” (Y. Stern, Zarahn, et al., 2008, p. 966).
On the one hand, given that all cognitive functions must also be realized by physi-
cal brain processes, the distinction between cognitive and brain reserve is not entirely
precise, and, if taken too literally, might be misleading. On the other hand, the con-
cepts of cognitive versus brain reserve nonetheless appear to depend on different
levels of analyses. Whereas brain reserve involves, as noted, particularly differences in
the quantity of the available neural substrate (e.g., brain size; number of synapses),
cognitive reserve especially involves between-individual and between-group differ-
ences in the organization and relative use of particular brain regions, such as sug-
gested by increased or decreased connectivity in brain networks, or the availability of
alternative networks to accomplish a given task. Another, more descriptively helpful,
term is that of “neurocomputational flexibility”:
This idea suggests that individuals who have developed a range of cognitive
strategies for solving complex problems, such as navigating around the neigh-
bourhood or performing well on neuropsychological tests, are more likely to
474 BRAIN AND ENVIRONMENT
remain within normal limits for longer despite the parallel progression of
underlying disease. Alternatively, high brain reserve individuals may not only
have a wider repertoire of conscious and preconscious cognitive strategies at
their disposal, but also a greater number of potential neural pathways for
execution of these same cognitive processes, thus allowing maintenance of
function despite neurological insult. (Valenzuela, 2008, p. 297)
As a concrete example, Scarmeas and Stern (2003) suggest that whereas a trained
mathematician or someone with lifelong engagement in mathematical training might
be able to solve a mathematics problem many different ways and so have more flexibil-
ity in solving the problem if any one strategy was precluded, someone with less train-
ing might have less “built in redundancy” and thus might demonstrate less resilience
in the face of brain damage. From this perspective, one might more accurately speak
of “brain reserves” or “cognitive reserves”—acknowledging that there are multiple
interacting mechanisms, operating at different spatial and temporal scales, and requir-
ing the assessment of both earlier and ongoing levels of complex mental stimulation.
This perspective is graphically summarized by the diagram in Figure 10.2, reprinted
from Valenzuela’s (2008) paper.
The latter ideas are closely linked conceptually to the further concept of compensa-
tion. The notion of compensation came to the fore after several early functional
neuroimaging studies found that there were clear differences in the patterns of neural
activation shown by healthy younger versus older adults performing the same cogni-
tive tasks. Often the difference could be characterized as involving more focal or local-
ized activations in the younger group, in contrast with more widespread and less focal
activations in the older group (e.g., Cabeza, 2002; Gutchess et al., 2005; J. M. Logan
Complex mental
activities
Brain
reserves
Neural and
Neurocomputational synaptic numbers
flexibility
et al., 2002; D. C. Park et al., 2003), with the results sometimes including both increases
in activation in the older relative to the younger group in some regions but also
decreases in other regions.
One pattern that has been frequently reported involves an increase in bilateral
brain activity in older persons compared with more unilateral activity in younger
adults during the performance of particular tasks. In healthy young adults, many
cognitive tasks, due to stimulus differences (e.g., words vs. pictures) or other cognitive
processing demands (e.g., involving the initial encoding vs. the retrieval of informa-
tion from memory), tend to predominantly recruit regions in either the left or right
cerebral hemisphere. For example, initially encoding to-be-remembered information
often elicits left-lateralized frontal activity, whereas right-lateralized activity may be
more often observed during retrieval, a pattern summarized by the Hemispherical
Encoding Retrieval Asymmetry (HERA) theory forwarded by Tulving and colleagues
(1994). Several studies have reported that such asymmetric activity is attenuated
in older adults, especially in prefrontal cortex. Older adults frequently show more
bilateral or “even-handed” involvement of both cerebral hemispheres in such tasks
(e.g., Rosen et al., 2002; also see Springer et al., 2005).
Cabeza (2002; see Dennis & Cabeza, 2008, for review) summarized this age-related
difference with the phrase “Hemispheric Asymmetry Reduction in OLDer adults,”
abbreviated as “HAROLD.” To illustrate, Cabeza, Grady and colleagues (1997) found
that whereas younger adults showed right lateralized prefrontal cortical activity
during the recall of word associate pairs, older adults showed bilateral prefrontal activ-
ity during recall. Other investigators have reported similar outcomes, using recogni-
tion tests rather than recall (e.g., Madden et al., 1999) and pictures rather than words
(e.g., Grady, Bernstein, Beig, & Siegenthaler, 2002). Age-related changes in the degree
of asymmetry also have been reported in more posterior brain regions, with both left
and right temporoparietal and frontal regions showing positive correlations with
accurate recognition of faces in older adults, whereas these effects were more lateral-
ized to the left hemisphere in younger adults (Grady et al., 2002). More purely percep-
tual decisions, such as required during a face-matching task, also have been found to
lead to greater bilateral prefrontal cortical activity in older than in younger adults
(e.g., Grady, McIntosh, et al., 2000).
One account of these patterns focuses on the notion of “dedifferentiation”—a
reduction in cerebral specialization accompanying the aging process, involving reduced
efficiency of specialized regional brain functioning, and perhaps arising from impair-
ments in inhibitory mechanisms across the corpus callosum,5 or for other reasons. The
dedifferentiation hypothesis is partially supported by neuropsychological data that
show that the correlations across different cognitive tasks tend to increase with aging,
suggesting decreasing specialization of function. For example, in a large-scale study,
Baltes and Lindenberger (1997) found that whereas in younger adults the median cor-
relation between five different composite ability measures tapping perceptual speed,
reasoning, memory, knowledge, and fluency was .38, the corresponding value for older
adults was markedly higher at .71, with corresponding differences in the amount of
explained variation of only 14% versus 50%.
The dedifferentiation hypothesis is also supported at quite a different level of
analysis: by neuroimaging findings showing that, compared with younger adults, older
476 BRAIN AND ENVIRONMENT
adults show reduced neural specialization in the ventral visual cortex (D. C. Park et al.,
2004). Although, like their younger counterparts, older adults showed some brain
regions that were particularly responsive to faces, and others that were particularly
responsive to other categories of stimuli, such as places, chairs, and pseudo-words,
across several different measures older adults had more shared voxels across catego-
ries than did young adults. This finding is important in that visual cortex is relatively
less affected by age than is frontal cortex, and it suggests that dedifferentiation may
be a pervasive aspect of aging (but see also Voss et al., 2008, for evidence that reduced
neural specialization may be particularly prominent for face and place stimuli, in con-
trast to color or word stimuli). More recently, J. Park and colleagues (2010) demon-
strated that such dedifferentiation at the level of neural representations was predictive
of flexibility in cognitive-behavioral performance. These researchers used a measure of
“neural specificity,” derived using the technique of multivariate pattern analysis of
fMRI activations. The measure of neural specificity significantly predicted the perfor-
mance of older adults on a number of different behavioral tasks requiring fluid, on-
the-spot processing, such as a task switching sequencing task and a verbal fluency
measure. Furthermore, whereas the neural specificity measure did not correlate with
a measure of longer term “crystallized” knowledge (vocabulary), it accounted for 30%
of the variance in a composite measure of fluid processing ability. These authors con-
cluded that “neural specificity may be a fundamental neural measure associated with
performance on complex cognitive tasks” (J. Park et al., 2010, p. 9258) and that
declines in neural specificity may be one of the neural factors that contribute to
age-related deficits in behavioral performance.
An alternative, but not necessarily entirely mutually exclusive, account to the
proposal that more diffuse or distributed activity arises from dedifferentiation posits
that the activity is in some way compensatory. According to a compensatory account,
the more diffuse or distributed brain activity in older individuals offsets age-related
deficits through a strategic recruitment of alternative regions, or involves changes in
the supporting cognitive processes. This model is also motivated by a broad range of
evidence from studies showing that recovery of language and motor functions after
unilateral brain damage often involves the recruitment of the unaffected cerebral
hemisphere such that, following recovery, the functions become comparatively more
bilateral (for review, see Cabeza et al. 2002; T. A. Jones, Hawrylak, Klintsova, &
Greenough, 1998).
In an attempt to directly contrast the dedifferentiation and compensatory accounts,
Cabeza et al. (2002) compared the brain activity shown by two groups of older adults
to that of younger adults. One group of adults (“old-high”) was selected to take part
because, during a preexperimental screening session, they performed at a level similar
to that of younger adults on a battery of four memory tests, known to distinguish
older adults with low versus high memory functioning. In contrast, the second older
adult group (“old-low”) was selected because they performed at a level below that
shown by younger adults on the screening battery. Importantly, however, these two
older groups did not differ from one another on measures of executive function
and general intellectual function, including the Wisconsin Card Sorting Task, letter
fluency (FAS), mental arithmetic, and mental control. Both older groups and a group
of younger adults then took part in a positron emission tomography (PET) scanning
Making Br ain Paths to Agil e T h in k in g , Part 1 477
(2007, p. 566) suggest that it may be possible for rTMS to “interact with the normal
processes of brain plasticity that accompany damage or chronic disease” so as to
increase “the ability of the brain to undergo compensatory changes” that improve
behavioral function.
In addition to suggesting a pattern of hemispheric asymmetry reduction in older
adults, many neuroimaging studies point to a second consistent pattern that involves
a posterior-to-anterior shift in aging, recently termed “PASA” (S. W. Davis, Dennis,
Daselaar, Fleck, & Cabeza, 2008). Reduced brain activity in posterior cortical regions
together with increased activity in frontal regions in older compared with younger
adults was initially reported by Grady and colleagues (1994). In two PET studies these
investigators found that, in comparison with a younger group, older adults showed
reduced occipital activity but increased prefrontal and also relatively more anterior
activity (including in occipitotemporal and parietal regions) during a perceptual
face-matching task and also during a location-matching task. In their report, Grady
et al. (1994) suggested a compensatory account of these findings:
The regions of cortex more activated in young subjects were early in the
visual pathway (prestriate), possibly before the ventral-dorsal dissociation,
and those more activated in the old subjects were in occipitotemporal, pre-
frontal, and parietal cortex. These results suggest that the neurobiological
changes that underlie the performance decrements of old subjects on these
visual tasks are a reduction in the processing efficiency of prestriate occipital
cortex, increased utilization of one or more cortical networks to compensate
for this inefficiency, and a concomitant slowing of reaction time, reflecting
the increased time for information processing by these recruited areas.
(Grady et al., 1994, p. 1461)
Although not invariably observed, subsequent studies, using tasks involving atten-
tion, perception, and episodic and working memory, have likewise reported a relative
shift from posterior toward comparatively more anterior activations in older adults
(e.g., Daselaar et al., 2003; Levine et al., 2000; see Dennis & Cabeza, 2008; D. C. Park
& Reuter-Lorenz, 2009, for review). However, interpretation of many studies may be
complicated by the potential contributions of age-related differences in task difficulty.
If a given task is more difficult for older persons, or is perceived to be more difficult,
this might well lead to increased anterior and especially prefrontal cortical involve-
ments, similar to those found with increasing task difficulty in younger adults
(e.g., Konishi et al., 1998). Additionally, strong claims about the functional relevance of
the age-related posterior to anterior shift require a conjunction of observations
regarding the relationship between prefrontal versus occipitotemporal activations,
such that age-related increases in prefrontal activation are shown to correlate posi-
tively with performance, and also that the prefrontal and occipitotemporal activations
are themselves negatively correlated with one another—as would be expected if
decreases in the latter are being compensated for by increases in the former.
In a recent fMRI study that included both an episodic recognition task and
a visual perception task, S. W. Davis et al. (2008) attempted to stringently evaluate the
posterior-to-anterior shift in aging hypothesis. These researchers further sought to
480 BRAIN AND ENVIRONMENT
examine the feasibility of applying the hypothesis to the patterns of age-related brain
deactivation (rather than activation) that were observed during task performance
(see the discussion of the “default mode” network in the “Between Tasks” section of
Chapter 9). To address the task difficulty issue, these researchers used a combination
of several steps. The steps included repeated encoding presentations compared with a
single presentation of the to-be-remembered words for the older versus the younger
group and a pair-wise accuracy matching procedure, such that even though both
groups showed a range of performance accuracies, pairs of older and younger adults
were selected who were matched very closely on their accuracy level.6 In addition, par-
ticipants were asked to give confidence ratings, both for the recognition memory task
(old/new judgments) and the visual perception task (judgments concerning which of
two colors extended over a larger area), thereby enabling examination of outcomes for
both low- and high-confidence responses.
Consistent with the posterior-to-anterior shift account, combining across the two
tasks, younger adults showed significantly greater activation in midline occipital
cortex (BA 17/18) than did older adults, whereas older adults showed greater activa-
tion in more anterior regions, including left middle frontal gyrus (BA 45) and also a
parietal region (supramarginal gyrus, BA 39). This pattern was observed both for
responses made with low confidence and responses made with high confidence, and
for both the memory task and the perception task. In addition, in older adults, there
was a negative correlation between the level of activation in occipital cortex and the
middle frontal activation. That is, older adults with lower levels of activity in the pos-
terior visual processing region showed greater frontal activation; furthermore, in
older adults, the frontal activity significantly correlated with task performance. In
contrast, neither of these correlations was significant in the younger group. Notably,
the age-related patterns of task-related deactivation—at least partially reflecting, as
we saw in Chapter 9, activity levels in the default mode network—followed a broadly
similar pattern. Specifically, deactivation in the older compared with younger partici-
pants was less pronounced in a more posterior region (precuneus) of the default mode
network, but older participants showed comparably greater deactivation in a more
anterior region (medial prefrontal cortex) of this network.
The evidence reviewed thus far clearly suggests that at least some (even if not all)
instances of reduced lateralization and/or the posterior-to-anterior shift in older com-
pared with younger adults reflect a process of compensation. Nonetheless, these find-
ings still leave unanswered an important question regarding the functional-behavioral
origins of that compensatory activity, and the extent to which such changes are inten-
tionally versus more automatically or unintentionally elicited. Does the additional
recruitment of brain areas arise because of deliberate or conscious efforts by individuals
to engage in different task strategies to boost their performance? Or does the additional
recruitment occur without any conscious awareness of the changes and without higher
order intentions? Stated differently (and not in an entirely parallel manner), is compen-
sation best construed as a psychological or as a brain-based phenomenon? Cabeza
(2002) dubbed these two possibilities as the “psychogenic” view, according to which
age-related changes in brain activity arise from age-related changes in cognitive struc-
tures or processes (such as semantic memory networks, or semantic elaboration during
encoding respectively) versus the “neurogenic” view, according to which age-related
Making Br ain Paths to Agil e T h in k in g , Part 1 481
brain activity changes reflect a change in neural architecture, including changes in the
functions of different brain regions, their connections, or both.
Definitively deciding between the psychogenic versus neurogenic accounts
“in general” is not possible, in part because it would require a highly detailed, veridical
mapping of the exact cognitive operations and processes that are used to complete a
given task by different groups—and then showing whether those operations are, or
are not, equivalent across the groups. It is also very likely that the particular contribu-
tors, at both the brain systems and cognitive-behavioral levels, to the several different
patterns of compensation that have been observed differ somewhat from task to task
and depending on context and other factors. Nonetheless, some broad forms of evi-
dence may weigh on one side or the other. To the extent that the task being examined
is very simple—allowing comparatively little leeway for between-person or between-
group strategy differences—finding age-related differences even on such tasks would
argue against the psychogenic and perhaps for the neurogenic perspective. Likewise,
to the extent that brain activity differences are observed regardless of overt or
instructed cognitive strategy manipulations, this also would support the neurogenic
perspective.
Relevant observations with respect to the latter possibility are provided by J. M.
Logan and colleagues (2002), who examined recognition memory in older versus
younger adults under different encoding conditions. These researchers found that pro-
viding older adults with additional encoding support—through encouraging deep
semantic elaboration of words by requiring participants to provide abstract/concrete
judgments—improved older adults’ recognition memory performance and also mark-
edly decreased the extent to which older adults showed less frontal activity than did
younger adults in left BA 6/44. Nonetheless, the more distributed bilateral activations
that they observed in older compared with younger adults remained, with older adults
in this condition still showing greater activation in right BA 6/44. This result thus
appears at least partially consistent with a neurogenic story.
A further finding that might weigh on the side of the neurogenic account comes
from a comparison of older and younger adults on a probabilistic category-learning
paradigm (the so-called weather prediction task), known to elicit activity in a neural
network involving the dorsolateral prefrontal cortex, caudate nucleus, and posterior
parietal cortex (e.g., Poldrack et al., 2001). On this task, older adults showed longer
response times overall, but measures of accuracy and of strategy use, based on block-
by-block analyses of participants’ response patterns, did not differ between the older
and younger groups (Fera et al., 2005). Yet whereas younger adults showed greater
prefrontal and caudate activation, older adults showed significantly greater parietal
activity than shown by younger adults, and, furthermore, this activity was positively
correlated with their performance. Age-equivalent performance on the task thus
appeared to be mediated by differential recruitment of regions within the same neural
circuitry without observable changes in accuracy or strategy application.
The latter findings suggest that the bases of at least some age-related differences in
activation patterns do not derive from relatively coarse-grained or obvious differences
in cognitive-perceptual processing. Nonetheless, it remains possible that more subtle
differences might be present and might be detected with measures with greater sensi-
tivity to detect strategy differences or other factors relating to the precise timing,
482 BRAIN AND ENVIRONMENT
EXPENDED RESOURCES
A
YOUNG CONSTRAINED
ADULT CUE REPRESENTATION
EARLY LATE
B
OLDER ADULT UNCONSTRAINED
VIA EXECUTIVE CUE REPRESENTATION
COMPROMISE
EARLY LATE
EMERGENT
LOAD-SHIFT EDITED
CUE REPRESENTATION
COMPENSATORY
STRATEGY
EARLY LATE
Under- Over-
recruitment recruitment
(decline) (compensation)
Aging Aging Aging
The figure also depicts two alternative accounts of the relations between age-related
declines in perception and cognition, including the “cascade” and the “common-cause”
views, that attribute age-related declines to decreased sensory processing versus
common brain-related changes, respectively.
In summary, although substantial initial steps have been taken, the exact origins
and timing of compensatory brain activity remain incompletely understood. An impor-
tant means to illuminating these issues may involve interventions aimed at stimulating
and training the use of broader networks. As observed by Reuter-Lorenz and Cappell
(2008, p. 181), “The brain is exceedingly clever, not only in the social, affective, and
cognitive states it supports, but in the neural strategies it invokes to develop and main-
tain these states effectively over the lifespan.” A key question thus becomes whether
and how we can “foster cognitive success and resilience in later life by discovering ways
to forestall or reverse declines, and otherwise optimize the brain’s response to its own
aging.” The next several sections evaluate what we know about some possible routes to
that goal. In addition, a broader conceptual overview of both the multiple sources of
functional and neural challenges during aging, and the multiple potential routes for
adapting to those challenges, is provided in Figure 10.5, which presents the “scaffolding
theory of aging and cognition” proposed by D. C. Park and Reuter-Lorenz (2009).
Crucially, as depicted in this model, the forms of compensatory scaffolding that we
have been considering in this section, including greater frontal cortical recruitment,
more distributed processing, and enhanced bilateral brain activity, are not the only
ways to combat the functional deterioration and neural challenges that aging so often
• Shrinkage
• Frontal recruitment
• White matter • Neurogenesis
changes • Distributed processing
• Cortical thinning Neural • Bilaterality
challenges
• Dopamine
depletion
Compensatory
scaffolding
Aging Level of
cognitive
function
Scaffolding
enhancement
• Dedifferentiation of
ventral visual area Functional
deterioration • New learning
• Decreased medial
temporal recruitment • Engagement
• Exercise
• Increased default
activity • Cognitive training
brings in its wake. Within the reach of many older persons are several additional forms
of scaffolding enhancement that can help to bolster the level of cognitive function
that is attained. Prominent in that set of options are new learning, cognitive training,
exercise, and engagement. The following sections consider indirect longitudinal and
epidemiologic research that has examined the potential ability of these options to
counteract aging-related cognitive decline and to sustain mental agility despite
advancing years. Direct experimental interventions exploring the question of how to
behaviorally bolster mental agility—at all ages—are also rapidly growing in number,
and these will be taken up in Chapter 11.
E D U C AT I O N
Precise evaluation of the potential effects of education on the maintenance of cogni-
tive functioning across age, and on the risks for dementia, has proven particularly
elusive. Despite early influential studies that provided a strong impetus for the notion
of education as a source of reserve (e.g., Albert et al., 1995; S. M. Butler, Ashford, &
Snowdon, 1996; Farmer, Kittner, Rae, Bartko, & Regier, 1995; Shimamura et al.,
1995), and an early and important proposal by Katzman (1993) that education
increases synaptic density in neocortical association cortex, thereby increasing brain
reserve, subsequent evidence has proven to be more mixed. As noted by J. W. King and
Suzman (2008, p. ii), “remarkably, the dose-response curve for education predicting
most outcomes is very poorly known, and just what the active ingredient is remains
unclear.” For example, in a meta-analysis of over 15 population-based studies,
Valenzuela and Sachdev (2006a, 2006b) found—consistent with the notion of educa-
tion providing a protective effect—that the overall odds ratio for developing dementia
related to higher education alone was 0.53 (95% confidence interval: 0.45–0.62).
However, of the 15 studies, whereas 10 studies showed a significant protective effect,
5 did not, and there was significant heterogeneity in the effects. Similarly, McDowell
and colleagues (2007, p. 127) remark on the “widespread, although interestingly not
universal” evidence that points to a link between level of education and the incidence
of dementia, particularly Alzheimer’s disease. These authors list outcomes from stud-
ies in seven different countries that have supported the link, but that are countered by
four studies from several different populations that did not support the link. Likewise,
Van Dijk and colleagues (2008) note that although “the most frequently mentioned
and well-established proxy measure of reserve capacity in the aging brain is educa-
tional attainment [. . .] it is noteworthy that recent articles based on longitudinal data
report conflicting results with respect to the relationship between educational level
and normal age-associated cognitive decline” (p. 119).
As noted, a wide array of correlated and potentially contributory factors make a
definitive determination of the magnitude and ultimate source of these across-study
488 BRAIN AND ENVIRONMENT
differences very difficult to assess. Although many factors may be important, one par-
ticularly important consideration with respect to evaluations of dementia is whether
diagnoses are determined based on psychometric test performance or on clinical
grounds: A relationship between education and psychometric test performance may
be observed that is not observed when the diagnosis is made on clinical grounds
(Gilleard, 1997). For instance, in a review of 34 studies, Anstey and Christensen (2000)
found that all seven studies that used mental status measures reported a protective
effect of education—an outcome that is important in that “mental status measures
are notoriously poor at reflecting change at the upper end of the score distribution”
(p. 167). In contrast, although protective effects of education were also found on mea-
sures of memory and on crystallized measures of intelligence, the effects were more
mixed (5/7 and 3/4 studies reported protective effects, respectively), and for the two
studies that measured fluid intelligence no beneficial effects were found. Thus, the
presence of protective effects of education may, in part, depend on the nature of the
outcome measure.
Another important consideration is the number of measurements used. Although
numerous studies examine only two test occasions, as noted by Van Dijk et al. (2008,
p. 120), “the use of three or more assessments of longitudinal cognitive aging reduces
measurement error and is the method of choice, especially when nonlinear effects are
expected.” Also important are health, stress-related, and lifestyle factors, and how and
if these are taken into account in analyses. Lower education or lower socioeconomic
status may be associated with higher levels of stress, in some cases for prolonged
periods of time (e.g., Seeman & Crimmins, 2001; see also the later section in this
chapter on “Socioeconomic Status, Stress, and Brain Paths to Agile Thinking”). These
increased levels of stress may be associated with increased glucocorticoids that—in
turn—may be linked to memory impairments and reductions in hippocampal volume
(e.g., Lupien et al., 2005). Proneness to psychological stress has also more specifically
been linked with an increased risk of Alzheimer’s disease (R. S. Wilson et al., 2003).
It is further worth noting that educational levels may themselves be determined by
varying individual, familial, and environmental factors; that education is many decades
removed from the time of cognitive or clinical evaluation; and that there is sometimes
ambiguity as to what comprises “lower” versus “higher” levels of education. Education
is most often based on self-report and dichotomized into levels involving less versus
more education. For example, the studies reviewed by Valenzuela and Sachdev (2006a,
2006b) most often separated groups into those with more, versus less, than 7 or 8
years of formal education. However, in a two-phase community study of nearly 500
older adults with middle- to high-socioeconomic status conducted in Ravenna, Italy,
DeRonchi et al. (1998) found that whereas the prevalence of dementia and Alzheimer’s
disease was higher among those with no formal education, there was no significant
difference in the prevalence of dementia for those who had at least 3 years, versus
more than 3 years, of formal schooling. In contrast, other studies have focused on
comparisons of the cognitive test performance of groups with much more extensive
formal education—contrasting groups with as many as 21 or 22 years of education
with those with 14 or 16 years (e.g., Shimamura et al., 1995) or less than versus more
than 16 years (e.g., Mortimer et al., 2003). Others have argued that, rather than years
of education, where the quality of educational experience might still vary considerably
Making Br ain Paths to Agil e T h in k in g , Part 1 489
even if correctly quantified, tests of literacy or reading level might constitute a better
predictor of cognitive decline than does education (Katzman, 1993; Manly et al.,
2005).
Nonetheless, recent outcomes also suggest that there is a real (albeit complex and
multifactor) association between education and dementia. McDowell et al. (2007)
using data from the Canadian Study of Health and Aging, with an initial sample of
6,646 persons, systematically evaluated possible artefactual contributors to the asso-
ciation between education and dementia. Participants living in the community were
screened at three time-points with 5-year intervals for mental status using the
Modified Mini-Mental State test (Teng & Chui, 1987), which has greater accuracy
(both sensitivity and specificity) than does the Mini-Mental State Examination
(MMSE; McDowell, Kristijansson, Hill, & Hébert, 1997). Individuals who scored
less than 78 on the screening test were given detailed clinical and neuropsychological
evaluations, with diagnoses based on a consensus between physicians and neuropsy-
chologists; in addition, clinical assessments of random samples of 983 persons who
screened negative were given.
The results, summarized in Figure 10.6, showed that there was a strong association
of education with the risk of dementia. For Alzheimer’s dementia, part of the asso-
ciation reflected other factors related to occupation, lifestyle behaviors, and socio-
economic status in general, but these factors alone did not entirely account for the
association. In addition, although the random sample of negative cases did show a
clear tendency to underidentify individuals with more education (of 16 cases of false
Incidence of demenita (per 1,000 person-years)
60
50
40
All dementias,
survivors + decedents
30
All dementias,
20 survivors only
Figure 10.6. Incidence of Dementia and Education Level. Data from the
Canadian Study of Health and Aging showing age- and sex-standardized 10-year
cumulative incidence of dementia per 1,000 persons as a function of educational level.
Cumulative incidence is shown separately for all types of dementia, Alzheimer’s disease
(AD), and vascular dementia (VaD). Reprinted from McDowell, I., Xi, G., Lindsay, J., &
Tierney, M. (2007, p. 132), Mapping the connections between education and dementia,
Journal of Clinical and Experimental Neuropsychology, 29, 127–141, with permission
from Taylor & Francis. Copyright 2007, Taylor & Francis.
490 BRAIN AND ENVIRONMENT
negatives, 7 at the first assessment and 9 at the second assessment, only 1 had less
than 8 years of education, whereas 15 had more than 8 years of education), the number
of missed cases was too small to offset the overall educational association. Based on
their systematic consideration of alternative accounts, the authors concluded that their
analyses “support the notion that educational attainment does influence risk of demen-
tia, both directly and through a number of intermediate pathways”—yet “more detailed
questions remain to be addressed.” For example, does education lower the likelihood of
cognitive decline or reduce the seriousness of the decline—or delay its onset? Also, “if
the effect lies chiefly for those with very little formal education, what accounts for this
non-linearity in the educational effect?” (McDowell et al., 2007, p. 139)
An association between education and dementia risk was also found in a recent
follow-up of 1,449 individuals between the ages of 65 and 79 years from four separate
independent population-based randomly selected samples in the Finnish Cardio-
vascular Risk Factors, Aging and Dementia (CAIDE) study. Ngandu et al. (2007) used
a three-step protocol, in which persons who scored 24 or less on the MMSE were then
clinically evaluated for dementia (according to the DSM-IV criteria) and then probable
and possible AD. Compared to persons with 5 years of formal education or less, those
with 6 to 8 years of education had a 40% lower risk of developing dementia; for per-
sons with 9 years of education or more the risk was 80% lower. These associations
remained unchanged after adjustment for several demographic, socioeconomic, vas-
cular, and lifestyle characteristics, such as smoking, physical activity, and occupational
characteristics; furthermore, a similar pattern (though slightly attenuated) was found
when analyses considered the entire sample (rather than only those available to the
follow-up), suggesting that although differential loss to follow-up might reduce the
magnitude of the association, it nonetheless remains significant.
Other forms of evidence such as twin studies, also point to the protective role of
education.9 Analyses of the association between education and risk of dementia in the
HARMONY study of the Swedish Twin Registry (Gatz et al., 2007) found that lower
education was associated with an increased risk of dementia in both a co-twin control
analysis and a case control analysis. In the co-twin analysis involving 33 monozygotic
pairs, the nondemented twin had, on average, 0.85 more years of education than his
or her demented twin partner, and the odds ratio was 3.17 (95% confidence interval
1.26 to 7.93); for the case control analysis the odds ratio was 1.77 (95% confidence
interval 1.38 to 2.28). Although, as shown in Figure 10.7, there was a marked overall
pattern for the average number of years of education to increase across birth years,
nonetheless in all birth years spanning from before 1909 to past 1929 the nonde-
mented members of the study population had more years of formal education than
did the demented members. Analyses using genotype data for the apolipoprotein
E genotype showed that the relation between education and dementia was not medi-
ated by genetics, but by shared environmental influences that were related to both
dementia and to education, potentially involving, for example, childhood factors, such
as nutrition or intellectual pursuits, or midlife factors, such as occupation.
It is possible that, at least in some cases, higher education (and other protective
factors, such as challenging occupations) may act to postpone the time at which
clinical symptoms of dementia become apparent. Stated differently, for a comparable
initial clinical symptom picture the degree of underlying brain pathology may be
Making Br ain Paths to Agil e T h in k in g , Part 1 491
10
6
19 09
19 10
19 12
19 14
19 16
19 18
19 20
19 –22
19 24
19 26
+
–2
29
9
–
<1
09
11
13
15
17
19
21
23
25
27
19
Birth year
Not demented Demented
Figure 10.7. Twin Study of Education Level and Dementia. Average years of
education for dementia cases, and nondemented members, by birth year, in the
HARMONY study of the Swedish Twin Registry. Reprinted from Gatz, M., Mortimer, J.
A., Fratiglioni, L., Johansson, B., Berg, S., Andel, R., Crowe, M., Fiske, A., Reynolds, C.
A., & Pedersen, N. L. (2007, p. 234), Accounting for the relationship between low
education and dementia: A twin study, Physiology and Behavior, 92, 232–237, with
permission from Elsevier. Copyright 2007, Elsevier.
greater in those with “protective” factors (Y. Stern, 2006). To the extent that this is
true, and there is more underlying brain pathology present, it might be expected that
once symptoms do appear such individuals would show more rapid progression of the
disease—leading to more rapid decline in cognitive function and earlier death than
seen in those without the “protective” factors.
Stern et al. (1999; see also Scarmeas et al., 2003; Seeman et al., 2005) presented
cognitive evidence supportive of this view, with greater (more rapid) yearly declines in
memory performance on a memory task (the Selective Reminding Test) observed for
those with more years of education (greater than 8 years vs. less than 8 years). Similar
results have been found for those with higher versus lower occupational attainment, and
higher versus lower levels of earlier leisure activity, though the time scale here was only
an average of 4 years before diagnosis (Helzner et al., 2007). Teri et al. (1995) also found
that for Alzheimer’s dementia patients, higher education was associated with more rapid
declines on the Mini-Mental State Examination and other dementia rating scales.
In an extensive study designed to examine the relations between education, the
neuropathology of Alzheimer’s disease (AD), and cognitive performance, Koepsell
et al. (2008) studied 2,051 participants, aged 65 years and older, from 27 different
Alzheimer’s Disease Centers who died and underwent autopsy, and all of whom had
taken the MMSE within 2 years of death. The severity of neuropathology was quanti-
fied with several measures, including the extent and distribution of neurofibrillary
492 BRAIN AND ENVIRONMENT
tangles (Braak and Braak stage), neuritic plaque density, and the Consortium to
Establish a Registry for Alzheimer’s Disease and National Institute on Aging/Reagan
diagnostic classifications. Consistent with the notion of a protective effect, higher
education (beyond high school compared with less than high school education) was
associated with higher final MMSE scores—but only when AD neuropathology was
absent or mild. For more advanced levels of AD neuropathology, there was little differ-
ence in the MMSE scores as a function of educational group, suggesting that the
advantages from higher education may not withstand the onslaught of more severe
neuropathology:
Considering four different potential mechanisms that might underpin the modu-
lating role of education on the association between Alzheimer’s disease and neuropa-
thology, Koepsell et al. (2008) concluded that the observed pattern might most likely
arise from both the effects of enhanced test-taking abilities in persons with more
education (“testmanship”) and greater cognitive reserve. As schematized in
Figure 10.8, Koepsell et al. (2008) suggest that, if the effects of differences in educa-
tion on test scores were entirely a result of education being confounded with some
other factor (or set of factors) that was, in fact, the “real” explanatory mechanism,
then, after identifying and controlling for that factor, there should be no relation
between education, severity of pathology, and test scores (Fig. 10.8A). If, instead, the
effects reflect factors related to test-taking ability, such as better test-taking skills,
more extensive knowledge, or greater abilities for abstraction, then the pattern to be
expected would involve an “across-the-board” advantage for the higher educated group,
regardless of level of pathology (Fig. 10.8B). The pattern that would reflect greater
cognitive reserve might look quite similar to that of better testmanship (Fig. 10.8C).
Greater neuroplasticity, if it takes the form that “attenuates the rate of decline in
cognitive performance over time, not just the timing of the first deficits,” (p. 1738)
might be expected to show the pattern depicted in the fourth case (Fig. 10.8D).
However, the actual results appear to reflect a composite outcome (Fig. 10.8E), sug-
gesting contributions from both enhanced test-taking abilities and from cognitive reserve.
Finally, and from a different perspective, we might also point to findings from
research that has sought to more directly examine the relationship between neuronal
structure and education, including ongoing involvement in learning opportunities. In
important early work, Scheibel and colleagues (Jacobs & Scheibel, 1993; Jacobs,
Scholl, & Scheibel, 1993) found a positive relation between dendrite size and educa-
tion in a cortical language area (Wernicke’s area). Postmortem analyses further showed
that deceased persons with a college education had more dendritic branches than did
those with only a high school education. However, as noted by Satz (1993, p. 282),
Making Br ain Paths to Agil e T h in k in g , Part 1 493
Cognitive performance
Cognitive performance
More educated More educated
Cognitive performance
More educated More educated
More educated
Less educated
Minimal Advanced
Severity of AD neuropathology
despite the “importance of these findings and the fact that they represent the
first evidence in humans linking concepts of educational experience and cognitive
reserve with dendritic regional arborization,” caution is clearly necessary in inter-
preting these outcomes given the relatively small sample size (20 neurologically
normal right-handers, 10 male and 10 female), marked intersubject variability, and
494 BRAIN AND ENVIRONMENT
the number of variables that were examined. Equally important, intriguing and
suggestive as these findings are, they are susceptible to differing causal interpreta-
tions10—Were individuals who had more dendritic branching more likely to complete
further years of formal education, or did more years of education lead to greater
dendritic branching?
SOCIAL INTERACTIONS
Beneficial effects on cognitive function also have been reported to be linked with
continued engagement in social activities, such as social interaction of various
sorts—with a spouse, contacts with relatives or friends (visiting, telephone, writing,
e-mail), and activity in social groups. In an early large-scale longitudinal study (Bassuk,
Glass, & Berkman, 1999), pronounced withdrawal or disengagement from social
activities was associated with increased risk of cognitive decline in a group of 2,812
community-dwelling older individuals (65 years of age or older) who were followed
over a period of 12 years. After statistically controlling for age and for initial levels of
cognitive function, initial levels of social disengagement were significantly associated
with the probability of cognitive decline (measured using the 10-item Short Portable
Mental Status Questionnaire) at follow-ups of 3, 6, and 12 years. In any given interval
tested, older individuals who reported fewer types of social contacts were more likely
to show cognitive decline, and were at increased risk of death, than were persons with
more social ties.
This association remained significant even after controlling for other sociodemo-
graphic and health characteristics, such as education, income, housing type, physical
disability, sensory impairment, and level of physical activity. Furthermore, social
disengagement still predicted cognitive decline even when the analyses were restricted
to those individuals who had shown a 6-year history of consistently high levels of
cognitive performance before the interval over which cognitive change was evaluated,
so as to minimize the effects of undetected or early dementia on the outcomes. The
odds of experiencing cognitive decline were nearly twice as great in the least socially
engaged individuals (those reporting no social ties) compared with those who were
the most socially engaged (those who reported five or more ties).
Similar outcomes were reported by Fratiglioni et al. (2000), based on a 3-year
follow-up of 1,203 individuals, living in the community, and using information regard-
ing social networks obtained by trained nurses at the outset of the study (at which
time all participants were dementia free). Clinical evaluations established 176
incident dementia cases (126 Alzheimer’s disease and 32 vascular dementia). Analyses
showed that there was a significant and systematically increasing risk of dementia as
the individual’s social network quality decreased, as assessed by a composite measure
of living arrangements and the frequency and judged quality of contacts (satisfying or
unsatisfying) with family and friends. After adjusting for age, sex, education, baseline
cognition, and depression, the relative risk associated with a poor or limited social
network compared with an extensive or moderate social network was 1.6 (95% confi-
dence interval 1.2–2.1): that is, a poor or limited social network increased the risk of
dementia by 60%. Similar findings were apparent for individual measures of social
connectedness. For example, individuals living alone, and those without any close
Making Br ain Paths to Agil e T h in k in g , Part 1 495
social ties, both had an adjusted related risk for developing dementia of 1.5 (95%
confidence interval of 1.0–2.1 and 1.0–2.4, respectively).
Using a case-control method in Japan, with 60 individuals with Alzheimer’s
dementia each matched on a pair-wise basis to two controls, Kondo et al. (1994) found
broadly similar outcomes, with a significantly greater odds ratio associated with
surrogate-reported low frequencies of psychosocial behaviors such as letter-writing or
telephoning and visiting friends or relatives. Analyses of several other community-
based prospective studies have also consistently pointed to the protective effects of
social integration on longevity and cognitive function (Seeman & Crimmins, 2001;
also see Fratiglioni et al., 2004; House, Landis, & Umberson, 1988; Lövdén, Ghisletta,
& Lindenberger, 2005; Menec, 2003). In a further study, Seeman et al. (2001) found
that, in an older adult sample that was initially selected for relatively high levels of
physical and cognitive function at baseline (the MacArthur cohort on successful aging)
a measure of the frequency of all social contacts did not predict performance on a
more detailed cognitive assessment battery. However, the frequency of specifically
emotionally supportive interactions with spouse, children, and close friends and
relatives was predictive (Seeman et al., 2001).
Other research, involving up to four annual assessments of some 800 individuals
in senior citizen facilities in and around Chicago, Illinois, revealed that the experience
of feeling lonely was related to clearly increased incidence of dementia, even after
statistically taking into account such factors as the frequency of social, cognitive, and
physical activity (R. S. Wilson, Krueger, et al., 2007). Loneliness, as assessed by five
5-point Likert-scale items, such as “I miss having people around,” and “I feel like
I don’t have enough friends,” also was associated with lower levels of cognitive func-
tion at initial assessment and with more rapid cognitive decline during follow-up.
One possible interpretation of these findings is that “loneliness is a consequence
of dementia, perhaps as a behavioral reaction to diminished cognition or as
a direct result of the pathology contributing to dementia” (R. S. Wilson, Krueger et al.,
2007, p. 238). However, various considerations argue against this interpretation;
for example, loneliness was unrelated to several indices of neural pathology, including
beta-amyloid plaques, neurofibrillary tangles, or cerebral infarctions. An alternative
explanation focuses on the possibility that loneliness might somehow compromise
the neural systems that subserve cognition and memory, “thereby making lonely
individuals more vulnerable to the deleterious effects of age-related neuropathology”—
that is, decreasing neural reserve (R. S. Wilson, Krueger, et al., 2007, p. 239).
Social interactions have the potential to yield both many emotional and many cogni-
tive benefits that may amplify and augment one another. Social activities offer indi-
viduals opportunities for a healthy commitment to broader aims and concerns, with
avenues for the expression of their own views and contributions. Participation in social
activities also may provide emotional support and resources for decision making and
problem solving. Finally, taking part in social interactions is itself frequently a challeng-
ing and dynamic cognitive activity that may draw on several cognitive and emotional
processes, such as attentional and inhibitory control, memory updating and monitor-
ing, and understanding of others’ perspectives and feelings (e.g., Adolphs, 2001).
From a biological perspective, several of the brain regions in the extensive system
of limbic and associational cortical and subcortical networks that are important to
496 BRAIN AND ENVIRONMENT
social cognition also support episodic and semantic memory, as well as other cognitive
functions. Thus, “it is possible that aspects of cognitive processing that allow people to
develop and maintain large social networks might also provide a reserve against the
development of cognitive impairment despite the accumulation of Alzheimer’s pathol-
ogy, or otherwise compensate for the effects of degeneration of non-social cognitive
systems” (D. A. Bennett et al., 2006, p. 411; also see Bickart et al., 2011; Kanai & Rees,
2011). Animal research has uncovered several detrimental effects of social isolation
on the brain, including decreased density of dendritic spines (dendrite branching) in
the hippocampus and the prefrontal cortex (Silva-Gómez et al., 2003) and down-
regulation of brain-derived neurotrophic factor—essential to synaptic plasticity—in
the dentate gyrus and CA3 regions of the hippocampus (Barrientos et al., 2003; see
especially the first section of Chapter 11); accompanying impairments in reversal
learning (Schrijver et al., 2004) have also been documented.
Recent analyses by Ybarra and colleagues (2008) of data from the Survey of
Americans’ Changing Lives (House, 1986, cited in Ybarra et al., 2008) demonstrated
that social interaction was a significant predictor of a measure of cognitive perfor-
mance, as measured by the MMSE, not only in older adults (aged 65–96 years) but also
in younger adults (aged 24–41 and 42–64 years). Notably, using an experimental
manipulation, these researchers also demonstrated that even a brief (10-minute)
experimental assignment to either a social interaction condition, involving discussion
of a social issue, or to a cognitively stimulating condition, involving a reading compre-
hension task, a crossword puzzle, and a mental rotation task, could boost cognitive
performance in healthy young adults (Ybarra et al., 2008, Study 2). Compared with
control participants who were assigned to watch 10 minutes of a situation comedy,
participants in both the social interaction and cognitive stimulation conditions
showed significantly higher speed of processing on a visual same/different judgment
task and achieved higher reading span scores on a working memory task. In the next
chapter we will consider several further cognitive experimental interventions that
may similarly enhance the cognitive performance of healthy young adults.
O C C U PAT I O N A L F A C TO R S
Other research points to the significant beneficial effects of engaging in forms of paid
employment that place high demands upon on-the-spot thinking and problem solv-
ing. An influential early series of studies (Kohn & Schooler, 1978) examined the effects
of complex work on cognition, using a combined set of measures that were designed
to tap—though clearly only partially and not entirely objectively—“flexible think-
ing.”11 Based on statistical analyses, using structural equation modeling, of longitudi-
nal data collected from a representative sample of American men across a decade
(1964 and 1974), Kohn and Schooler (1978) concluded that “job conditions offering a
challenge and the opportunity to do self-directed, substantively complex work increase
intellectual flexibility.” On the other hand, “work conditions that limit intellectual
challenge and self-direction on the job decrease intellectual flexibility” (Schooler et al.,
1999, p. 483). Findings based on a third testing of the original sample, collected in
1994 to 1995, pointed to a similar conclusion, even after the original sample had aged
a further 20 years.
Making Br ain Paths to Agil e T h in k in g , Part 1 497
More recent results from the Maastricht longitudinal study on aging, conducted in
the Netherlands and using independently assessed mental work demands for different
job categories (Bosma et al., 2003), provide stronger support for the possible protec-
tive effects of complex work on cognitive performance (see also Forstmeier & Maercker,
2008). Information on the mental work demands of various occupations was obtained
from an independent survey, in which 44,486 employees answered four questions on
the nature of their work. The questions were as follows: (1) Is your work mentally
demanding? (2) Do you have to concentrate strongly during work? (3) Does your work
require great precision? (4) Do you regularly work under time pressure? The average
percentage of “yes” responses to these questions was computed and then matched to
the job titles of 708 participants who had been professionally active outside of the
home and had a job title code (women who worked at home were excluded).
As expected, mental work demands and educational level were significantly posi-
tively correlated (r = .60). Comparisons of the cognitive performance for participants
with the greatest versus fewest mental demands at work (highest third vs. lowest
third) showed that, over the 3-year follow-up, those with the fewest mental demands
at work showed significantly greater declines in information processing speed,
memory, and general cognitive status as assessed by the MMSE. Although lower
educational levels also were associated with relatively greater declines in cognitive
functioning, these effects were markedly attenuated and, indeed, no longer signifi-
cant, after controlling for the effects of mental workload and, importantly, greater
mental workload had similar effects in the lower versus higher educated participants.
Three years after baseline, at which time none of the participants (aged 50–80) had
shown cognitive impairment, 4% of those with comparatively less cognitively demand-
ing employment developed some cognitive impairment compared with 1.5% of those
with mentally demanding jobs.
The outcomes of a study by Staff and colleagues (2004) that attempted to evaluate
both passive versus active reserve components as contributors to cognitive function
in older adulthood via brain imaging similarly underscore the importance of occupa-
tional attainment and challenges. (The distinction between passive and active reserve
was discussed earlier in this chapter in the section on “Brain Reserve, Cognitive
Reserve, and ‘Compensation.’”) The participants were 92 older volunteers, aged
79 years at the time of testing. They were a subsample of a 1932 Scottish Mental
Survey study (the 1921 Aberdeen birth cohort study) and included all those from the
cohort study who could be successfully imaged using MRI by Staff and colleagues. This
study contrasted the contributions of total intracranial volume, as a measure of
passive reserve, and education and occupational attainment, as measures of active
reserve, to memory performance (assessed using the auditory verbal learning test),
and nonverbal fluid reasoning (assessed by Raven’s Progressive Matrices). The analy-
ses also included measures of childhood intelligence (assessed at age 11) and age-
related pathology as measured by MRI. Total intracranial volume was not predictive of
either memory or fluid reasoning performance, but education was significantly predic-
tive of older adults’ memory performance, accounting for between 5% and 6% of the
variance. Occupational attainment was also predictive of memory performance,
explaining about 5% of the variance. In contrast to education, which did not predict
older adults’ reasoning abilities, occupational attainment also predicted nonverbal
498 BRAIN AND ENVIRONMENT
reasoning ability (between 5% and 8% of the variance). This study thus points to the
important potential reserve effects of both education and occupational attainment,
such that “more education and a more cognitively complex occupation predict higher
cognitive ability in old age than would be expected for a person’s childhood ability and
accumulated brain burden” (Staff et al., 2004, pp. 1196–1197).
Outcomes from another longitudinal study, the Canadian Study of Health
and Aging, generally concur with the earlier findings but also point to the potential
importance of the duration of complex work and the possibility that complexity of
work with people and things may differ from complexity of work predominantly
involving data (E. Kröger et al., 2008). After adjusting for work-related physical
activity and education, it was found that high complexity of work with people or things
was associated with a reduced risk of dementia or Alzheimer’s disease, but only for
individuals who held their principal occupation for more than 23 years (reductions of
64% and 55% for dementia, and 69% and 52% for Alzheimer’s disease for high
complexity work with people and things, respectively). In contrast, and surprisingly,
prolonged high complexity of work with data was associated with an increased risk of
dementia or Alzheimer’s disease, possibly reflecting elevated stress in these cases or
the absence of beneficial effects arising from social interactions.
Other researchers have suggested that the interpersonal aspects involved in higher
level occupations may play a particularly important role in the maintenance or buildup
of protective effects from sustained intellectually and interpersonally demanding
employment. In particular, Y. Stern et al. (1995) found that, among Alzheimer’s
disease patients who were matched on the severity of clinical expression of the
disease, those who had had occupations that involved more substantive complexity
and more interpersonal skills or had high physical demands (e.g., jobs requiring
eye-hand-foot coordination, climbing, balancing) showed greater deficits of parietal
blood flow—suggesting that the underlying disease process was more advanced
in these individuals before a comparative level of clinical deficits was apparent.
In addition, even after controlling for age, level of education, and disease severity,
both the interpersonal demands and physical demands of the previous occupation12
still accounted for unique variance in the measure of parietal function.
Protective effects against dementia of occupations involving higher complexity,
particularly occupations requiring the supervision of subordinates in the workplace,
were also found in a longitudinal study of the elderly conducted in Amsterdam
(Schmand et al., 1997)13. Similarly, benefits of intellectually demanding work and
higher levels of work-related human interaction and communication were shown in a
National Academy of Sciences study of World War II veterans (Potter et al., 2008).
This study involved a sample of 1,036 individuals who, in early adulthood, had been
given an assessment of intelligence through the Armed Services. These individuals
were then also tested, in late adulthood, via telephone as part of an epidemiologic
study of aging and dementia, during which they provided their occupational history
and completed the modified Telephone Interview for Cognitive Status (similar to the
MMSE, but including additional content, such as immediate and delayed recall of a
10-item word list). Multivariate regression models revealed that both intellectually
demanding work and higher levels of human interaction and communication at
work were each significantly associated with higher scores on the cognitive status test.
Making Br ain Paths to Agil e T h in k in g , Part 1 499
This study also reported an interaction between the general intellectual demands of
the participant’s work and intelligence, such that persons who had obtained relatively
lower intelligence scores in the early adulthood assessment achieved greater cognitive
benefits from an intellectually demanding occupation. The authors concluded that
these findings “support the notion that intellectually demanding work is more than a
proxy for education or intellect, and that it produces an independent association with
cognitive performance in later life” (Potter et al., 2008, p. 1806; see also Rohwedder &
Willis, 2010).
Taken together, these findings are consistent with an “environmental complexity”
hypothesis that was first forwarded by C. Schooler in the early 1980s (Schooler, 1984,
1998; Schooler & Mulatu, 2001; Schooler, Mulatu, & Oates, 1999). According to this
hypothesis, complex environments are those that:
Such environments will both invite and require high levels of cognitive effort,
integrative thinking, and planning and coordination. They also are likely to motivate
individuals to develop their intellectual capacity and skills in ways that could be
generalized to other situations. They are, then, environments that will ask for, and
continuously encourage, agile thinking.
L E I S U R E A C T I V I T I E S A N D A G E - R E L AT E D C O G N I T I V E D E C L I N E
In an extensive review of cohort studies that examined the effects of education,
occupation, premorbid intelligence, and mental activities on the risk of dementia,
Valenzuela and Sachdev concluded that, of all these indices, the forms of leisure
activities individuals engaged upon most consistently emerged as highly important.
“It is evident that mentally stimulating leisure activity is the most robust brain-reserve
measure, since all these studies showed a significant protective effect even after
controlling for age, education, occupation and other confounds” (Valenzuela &
Sachdev, 2006a, p. 447). Several of the studies included in their review will be consid-
ered here. Nonetheless, there are also both less strongly supportive findings and a few
instances of negative findings with regard to the benefits of leisure activities particu-
larly with respect to reducing age-related cognitive decline—rather than dementia
risk, for which the evidence is much stronger. Negative and comparatively less strongly
supportive findings with regard to age-related cognitive decline will be considered
first, followed by more positive findings, and thereafter by a separate consideration of
the effects of cognitively stimulating leisure-time activities on dementia risk.
Newson and Kemps (2005) used a composite measure of current activities, includ-
ing items related to household maintenance, domestic chores, social activities, and
service to others in both cross-sectional and longitudinal analyses of a subset of data
(N = 755) from a population-based study of older adults in Australia. The cross-
sectional analyses showed that, after controlling for the effects of sensory functioning
(visual and auditory acuity), a generally active lifestyle was associated with higher
levels of current cognitive function, though the effects were not large (increases of
between 3% and 5% in total variance explained on measures of speed of processing,
picture naming, incidental recall, and verbal fluency). A commonality analysis,
performed to partition the variance into unique and shared proportions, including
age, sensory function, and activity, showed that the total variance accounted for by
activity ranged from 5% to 14%. Similar modest beneficial effects of engagement were
observed in the longitudinal analyses from data collected across a 6-year interval.
After controlling for effects of sensory functioning, general lifestyle activity level pre-
dicted change scores on measures of processing speed (1%), picture naming (3%), and
incidental recall (3%).
In the United Kingdom, Gilhooly and colleagues (2007) conducted an examination
of the relations between mental activities and fluid reasoning in a sample of 145 older
participants, aged 70 to 91 years. These researchers reported a significant positive cor-
relation (r = .26, p < .01) between a composite score of mental activities and a fluid
intelligence factor score derived from several cognitive tests. In addition, simultaneous
multiple regression showed that mental activity levels made a separate contribution to
predicting current fluid functioning, in addition to contributions from other factors
(age, National Adult Reading Test score, and a measure related to socioeconomic status).
Notably, during an interview with the participants, the researchers also asked most of
the participants the question “Is there anything you deliberately do to maintain your
mental functioning?” There was evidence that individuals who reported that they delib-
erately engaged in mental activities showed a reduced negative effect of age on both
abstract fluid reasoning tasks and a measure of real-world problem solving—even
though this group did not differ from nondeliberate engagers in the sheer volume of
mental activities reported. The researchers speculate that perhaps “deliberate engagers
undertook more meta-cognitive processing and monitored and reflected more on their
own performance in order to identify useful strategies for solving problems, making
decisions and storing and retrieving information” (Gilhooly et al., 2007, p. 276).
Other studies suggest that it may be that some subgroups of older adults especially
benefit from increased cognitively stimulating leisure activities. For example,
Christensen et al. (1996) found greater activity-related benefits for participants with
low educational attainments. Similarly, Gilhooly et al. (2007) found that the beneficial
effects of leisure-time involvement were stronger for those participants who were
from the relatively most economically deprived areas (based on their postal codes)
compared to those from relatively affluent areas. Leisure activity was significantly
positively related to fluid intelligence measures for both groups, but to real-world
problem solving only for the less advantaged group.
Other efforts have focused on obtaining more precisely scaled measures of cogni-
tive activity and also on trying to include lifetime, rather than only cross-sectional,
measures of cognitive and other activities. R. S. Wilson et al. (2003) developed
Making Br ain Paths to Agil e T h in k in g , Part 1 503
In this same spirit, it is essential to keep in mind that there are multiple metrics on
which the value of an activity may be assessed. Additionally, for reasons that remain
504 BRAIN AND ENVIRONMENT
to be fully elucidated, some metrics, such as age-related cognitive decline, may prove
less uniformly sensitive to the differential effects of cognitively stimulating leisure
activities than are other metrics, such as dementia risk. It is to this latter outcome
measure that we next turn and where we find more robust support for the benefits of
ongoing involvement in a diversity of cognitively and socioemotionally challenging
pursuits.
dementia decreased by 33% for each 1-point increase in the composite cognitive
activity measure. For example, for a person reporting a high level of cognitive activity
at baseline (scoring at the 90th percentile for cognitive activity) the relative risk of
developing Alzheimer’s was 47% less than for a person who reported infrequent
cognitive activity at baseline (scoring at the 10th percentile). Similar outcomes
were obtained when excluding participants with especially low levels of episodic
memory at baseline (a possible very early sign of disease), and when including a
variable coding for the possession of one or more genetic risk factors potentially
related to Alzheimer’s disease, as well as when adding additional terms for depression
and other illnesses.
Higher cognitive activity levels also were associated with significantly attenuated
declines in cognitive function. For example, whereas, on average, the global cognitive
function score decreased by 0.043 units per year, the decrement was about 0.046 units
per year for someone in the 10th percentile of cognitive activity but only 0.026 for
someone in the 90th percentile of cognitive activity. More frequent cognitive activity
was associated with higher baseline function for each of several cognitive domains
examined, and it was associated with lower rates of decline for working memory,
perceptual speed, and (less strongly) episodic memory, but not for semantic memory
or visual-spatial ability. Although there are multiple possible interpretations, Wilson
et al. (2002) suggest that one possible interpretation of the latter findings is
that strengthening working memory and/or perceptual speed may help to offset or
compensate for age-related decline in other functions.
In their meta-analysis of some 22 studies, involving combined results for more
than 29,000 persons, Valenzuela and Sachdev (2006a) found that high levels of mental
activity, as determined by educational level, occupational complexity, or cognitive
lifestyle activities, resulted in an overall relative risk reduction of incident dementia of
46%. The odds ratios for these three different indices were quite similar to one another
(0.53 for years of education, 0.56 for occupational complexity, and 0.50 for cognitive
lifestyle). Very similar patterns were found when, rather than dementia incidence, the
outcome variable was cognitive decline. More recent studies reviewed by Valenzuela
et al. (2007) have concurred in the estimates of a protective effect for incident demen-
tia associated with cognitive activity especially later in life. Protective effects of
between 40% and 50% were observed after simultaneously controlling for other risk
factors, such as age, and earlier life experiences (e.g., level of education). Across six
studies with individual sample sizes between 469 and 2,040, and a combined N of
7,061, increased cognitive activity in later life was associated with an adjusted risk of
dementia between 0.41 and 0.67.
Further bolstering the inference that it was mentally stimulating activities, in par-
ticular, that were beneficial, in several of these studies (Fratiglioni et al., 2000;
Fabrigoule et al., 1995; Karp et al., 2006; Verghese et al., 2003) cognitive lifestyle
activities were related to incident dementia in a dose-dependent manner, such that
the higher the level of stimulating activities (e.g., the cognitively challenging leisure
pursuits were undertaken frequently rather than rarely), the greater the reduction in
risk. In their 21-year prospective study as part of the Bronx Aging Study, Verghese
et al. (2003) found, for example, that a one-point increase in the cognitive-activity
506 BRAIN AND ENVIRONMENT
Later, in Chapter 11, we will explore the beneficial effects of several direct, experi-
mental interventions that aim to increase attention and control processes on cogni-
tive and self-regulatory performance—including not only in older adults but also in
preschool children and in healthy young adults.
Making Br ain Paths to Agil e T h in k in g , Part 1 507
If this model is correct, then bilinguals have had massive practice in exercis-
ing inhibitory control, an experience that may then generalize across cogni-
tive domains. If the boost given by childhood bilingualism is sufficiently
strong, bilingualism may continue to influence certain control processes
throughout the life span. (p. 291)
WM cost (ms)
1050 1050
900 900
750 750
600 600
450 450
300 300
150 150
0 0
30–39 40–49 50–59 60–69 70–79 30–39 40–49 50–59 60–69 70–79
Age Age
(c) 1500
Simon effect (Inhibition)
1350 Monolingual
1200 Bilingual
1050
900
750
600
450
300
150
0
30–39 40–49 50–59 60–69 70–79
Age
and the Simon effect (third panel) were more pronounced for persons in the older age
brackets (60–69 and 70–79 years).
Two other studies reported by Bialystok et al. (2004) replicated the central finding
of an increased resistance to interference (a smaller Simon effect) in bilingual com-
pared with monolingual participants even though, as in the study just reviewed, the
two groups were otherwise comparable on background measures and experience.
These outcomes—together with the unexpected observation that bilingual language
use also was beneficial more generally for the four-color condition that placed especial
demands on working memory—suggest that the executive processes that are called
upon to successfully and fluently manage two languages are also called upon in the
Simon task. The researchers speculate that:
These executive processes may not be neatly partitioned into parts that
deal with inhibitory control and others that are concerned with working
memory—it may be a more generalized set of control processes that manages
510 BRAIN AND ENVIRONMENT
significant, when confining the analyses to only those participants who had immi-
grated (average onset of 63.8 years for monolinguals vs. average onset of 75.3 years
for bilinguals). Finally, unlike the findings suggesting a faster rate of cognitive decline
(especially in executive speed and memory) in those with more versus fewer years of
formal education that were reported by Scarmeas and colleagues (2006), follow-up
analyses of the patients’ MMSE scores across the 5 years following the diagnosis
provided no evidence that there was a faster rate of cognitive decline in the bilingual
than in the monolingual group.
There are several reasons to be cautious in interpreting these outcomes—especially
given that, like many of the studies considered in the current chapter focusing on
indirect evidence, the study is correlational rather than experimental. Nonetheless,
Bialystok et al. (2007) rightly note that the factors that led participants to be bilingual
rather than monolingual predominantly occurred quite early in life, and this differs
from other factors, such as reduced midlife activity, that might more directly influence
subsequent cognitive function or potentially contribute to dementia (as in the research
reported by Friedland et al., 2001). Broadly in line with the views taken by many of the
researchers reviewed throughout this chapter, Bialystok et al. (2007, p. 463) reach
the speculative conclusion that “bilingualism does not affect the accumulation of
pathological factors associated with dementia, but rather enables the brain to better
tolerate the accumulated pathologies.”
Further support for the potentially beneficial effects of lifelong use of more than
one language is provided by a large-scale epidemiological study of older adults in Israel
that used representative sampling procedures and cognitive-screening measures
across three testing occasions over a period of 12 years (Kavé et al., 2008). These
researchers found that, on each of the three testing occasions, the number of lan-
guages that were spoken significantly contributed to measures of cognitive status,
above and beyond what could be predicted on the basis of other demographic factors
such as age, education, or age at immigration. Speaking multiple languages was also a
predictor of cognitive status in persons who had had no formal education.
The mechanisms that contribute to such protective effects remain to be fully deter-
mined, and only some of several possibilities have been considered here (e.g., func-
tional reorganization of brain networks; see Valenzuela & Sachdev, 2006a, and
Mercado, 2008 for a review of additional possibilities). Nonetheless, there is growing
evidence that the use of more than one language may require individuals to continu-
ously practice using inhibitory and other control processes that, in turn, may help
counteract the deleterious effects of cognitive aging. (See Kroll et al., 2008 for recent
review of neuroimaging and neurophysiological evidence relating to language selec-
tion; also see Emmorey, Luk, Pyers, & Bialystok, 2008, for evidence that, unlike two
languages within a single modality, two languages in different modalities, with one of
the languages involving spoken language but the other the motor-system signs of
American Sign Language that do not compete for “articulation” in the same manner,
is not associated with a corresponding enhancement of executive control function.)
More generally, Bialystok et al. (2007, p. 463) conclude that “it is increasingly clear
that biological factors interact with environmental experiences to determine cogni-
tive outcomes; the present findings suggest that bilingualism is one experiential factor
that can provide a positive benefit in this respect.”
512 BRAIN AND ENVIRONMENT
Protective effects from physical activity for the risk of dementia also have been
shown. Data from a randomly selected community sample of men and women aged
65 years or older, collected as part of the Canadian Study of Health and Aging,
a prospective study on dementia, showed that, compared with no exercise, physical
activity was associated with lower risks of cognitive impairment, Alzheimer’s disease,
and dementia of any type; after adjusting for age, sex, and education the odds ratios
were 0.58, 0.50, and 0.63, respectively (Laurin et al., 2001). Likewise, in a randomly
selected subsample of a larger population-based cohort in Finland (the CAIDE or
Cardiovascular risk factors, Aging, and Incidence of Dementia study), Rovio et al.
(2005) found that participating in strenuous leisure-time physical activity at least twice
a week in midlife was associated with significantly reduced risk of both dementia and
Alzheimer’s dementia at follow-up—even after adjustments were made for age, sex,
and education, and a number of health and lifestyle factors (smoking, alcohol drinking)
and also for APOE genotype (odds ratio for dementia of 0.48, 95% confidence interval
of 0.25–0.91; odds ratio for Alzheimer’s dementia of 0.38, 95% confidence interval of
0.17–0.85). Reduced risk for incident dementia in those who self-reported exercising
three or more times a week compared to fewer than three times a week also was found
in a large 6-year prospective cohort study by Larson and colleagues (2006).
Nonetheless, as for each of the other potentially protective factors that we have
considered in this chapter, there are also some negative findings. For example, in their
prospective study of Catholic clergy that demonstrated clear protective effects of
greater cognitive activity on dementia risk, R. S. Wilson et al. (2002) found no
evidence for protective effects of physical activity for either incidence of Alzheimer’s
disease or for cognitive decline. Similarly, although, in a Japanese study, Yoshitake
and colleagues (1995) found that physical activity was related to somewhat decreased
risk of Alzheimer’s disease, they did not find a reduction of risk for vascular dementia.
Relatively small sample sizes, and consequently comparatively low incidence rates of
dementia, may contribute to some reported negative findings. However, as also for
the other factors that we have considered, experimental interventions—to be taken
up in our next chapter—will substantially strengthen the evidence base supporting
the roles of physical exercise and cardiovascular fitness in sustaining and promoting
mental agility in persons of all ages.
Similar findings emerge with respect to school achievement. Analyses combining data
across several large-scale nationally representative cross-sectional surveys showed
that, compared to nonpoor children, poor children between the ages of 5 and 17 years
were twice as likely to repeat a grade, and twice as likely to be expelled or suspended
from school; they were also 2.2 times as likely to not finish high school (Brooks-Gunn
& Duncan, 1997).
Multiple interrelated factors are associated with differences in socioeconomic
status and income (cf. McEwen & Gianaros, 2010). Clearly, poverty may lead to funda-
mental physical deprivation if families possess insufficient resources to meet their
basic needs for food, clothing, and shelter. Poverty also leads to increased exposure to
stress, and decreased access to diverse forms of cognitive stimulation. The confluence
of multiple adverse conditions—physical, socioemotional, and cognitive—may be “a
key, unique feature of childhood poverty” (G. W. Evans, 2004, p. 86; G. W. Evans &
English, 2002). Low-income compared with middle-income children are exposed to
greater levels of violence, and of family disruption, and they experience more numer-
ous and higher levels of many forms of adverse physical conditions in their homes and
neighborhoods (Aneshensel & Sucoff, 1996). Such adverse conditions range from
increased exposure to air, water, and noise pollution, to inadequate heating in the
winter, to more frequent safety hazards within and outside the home, such as greater
traffic volume, more crime, and less playground safety, with fewer elements of nature
(G. W. Evans, 2004; Strife & Downey, 2009). Notably, as we will see in Chapter 11, in
the section on “Attention Restoration Theory and Experiences of the Natural
Environment,” even relatively brief exposure to natural elements, such as trees or
parks, may help to buffer individuals against the detrimental physiological and cogni-
tive effects of stress; the experience of natural elements may also specifically help to
restore capacity for directed attention, which might have additional carryover effects
on further activities, such as classroom learning and engagement.
The amount and forms of the cognitive stimulation that children receive, both
through speech and interactions with their parents and through the availability and
diversity of books, toys, activities, and experiences such as travel and cultural events,
differ considerably with socioeconomic level (Bradley et al., 2001). Children from poor
families have been found to have less access to a wide range of different recreational
and learning materials, beginning in infancy and continuing through adolescence. At
all ages (infancy, early childhood, middle childhood, and adolescence) children from
poor families are far less likely to have three or more children’s books (Bradley et al.,
2001); they are less likely to go on trips or to visit a library or museum, and they are
less likely to be given lessons to enhance their skills in domains such as music or
sports.
Thus, poverty limits children’s access to developmental stimulation and heightens
their exposure to stress—both physically and psychosocially (Dearing, 2008). As fur-
ther developed later in this section, such stress is shown biologically: Children from
lower socioeconomic (SES) levels tend to show higher levels of the steroid hormone
cortisol, which in humans is associated with the action of the hypothalamic-pituitary-
adrenal axis stress response system (G. W. Evans & English, 2002; Lupien et al., 2001).
Poverty also leads to heightened parental stress, associated with parental factors such
as depressive symptoms that, in turn, lead to changes in parenting behaviors that may
Making Br ain Paths to Agil e T h in k in g , Part 1 515
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These outcomes are consistent with the possibility that the environmental
deprivation and stress associated with the life experiences of low SES children may
particularly adversely affect prefrontal cortex development. Both the attenuated early
attention-sensitive components and the reduced ERP novelty response parallel those
found in patients with lateral prefrontal lesions (Barceló et al., 2000; Yago et al., 2004).
On neuropsychological testing, children from lower SES also showed reduced working
memory span as assessed by digit span (with the scaled performance of the higher
SES children exceeding norms by more than one standard deviation, but that of lower
SES children near the mean) and reduced flexibility on the alternating portion of the
Trail Making test. The latter task, in which the test-taker must alternate between
marking sequentially increasing numbers versus letters, requires both set shifting and
inhibition. In contrast, no impairments in the performance of the lower SES children
were observed on the simpler noninhibitory portion of the Trail Making test that
required attention to numbers only, rather than intermixed numbers and letters.
The relation between childhood poverty, chronic stress, and cognitive function,
specifically working memory, in young adults has also more explicitly been demon-
strated in a recent investigation that used a biological measure of chronic physiologi-
cal stress. Drawing on results from a longitudinal study on rural poverty, G. W. Evans
and Schamberg (2009) were able to obtain data for 195 young Caucasian adults on the
duration of childhood poverty exposure, their working memory, and a measure of
“allostatic load”—“an index of cumulative wear and tear on the body caused by
repeated mobilizations of multiple physiological systems over time in response to
environmental demands” (p. 6545). As noted by McEwen (2008, p. 175), the term
“allostatis” refers to the “active process by which the body responds to daily events
and maintains homeostasis” or is able to achieve “stability through change.” Adaptive
responses to sudden unexpected or stressful events, such as increased catecholamines
(e.g., norephinephrine) that increase heart rate and blood pressure, if chronically
increased or dysregulated, may lead to disease. The notion of “allostatic load,” or “over-
load,” was introduced by McEwen and colleagues to refer to “the wear and tear that
results from either too much stress or from inefficient management of allostatis,” such
as not turning off the response when it is no longer needed or not habituating
to a recurrent stressor and so not attenuating the allostatic response (McEwen, 2008,
p. 175; see also Ganzel, Morris, & Wethington, 2010).
Allostatic load thus reflects an organism’s attempt to maintain bodily equilibrium
in multiple response systems (e.g., cardiovascular, endocrine, neuronal), and it was
assessed by G. W. Evans and Schamberg (2009) as the sum of six risk factors on which
the participant scored above the median, including resting diastolic and systolic blood
pressure, overnight cortisol, overnight epinephrine and norepinephrine, and body
mass index. Each of these physiological measures, and the summary measure of allo-
static load, were assessed at age 9 years, and again at age 13 years, with chronic allo-
static load computed as the average across the two assessments. Working memory was
assessed at age 17 years, and it was computed as the maximum number of visually
spatially presented stimuli that the participants could recall in correct sequential
order, averaged across two assessments (separated by 1 hour).
Results showed that, the greater the proportion of a child’s life growing up in
poverty (measured at birth, 9, 13, and 17 years), the higher the degree of cumulative
wear and tear on his or her body. In addition, there was a significant negative relation
520 BRAIN AND ENVIRONMENT
between the proportion of life in childhood poverty and working memory scores in
young adulthood. This relation between poverty and working memory was signifi-
cantly attenuated when childhood allostatic load was added to the regression equa-
tion. Furthermore, allostatic load during childhood significantly predicted working
memory in young adulthood.
Although these studies all provide evidence that is correlational, and so interpreta-
tive caution is clearly necessary, findings from other sources and using other techniques
broadly support proposals that “family income per se influences family investments in
children, family stress processes, and, in turn, children’s psychological development”
(Dearing, 2008, p. 328). For example, in a number of U.S. states in the late 1960s to
early 1970s, randomly selected families who fell below prespecified income levels were
“negatively taxed”—that is, given an income allowance. In addition to more direct
health benefits (e.g., improved nutritional adequacy in rural sites in Iowa and North
Carolina, and fewer children with low birth weight in the Gary, Indiana site), compared
with children in control group families, children in the experimental group showed
improved school attendance (rural and Seattle/Denver sites), improved academic grades
(Gary site, grades 7 to 10), and higher achievement test scores (rural and Gary sites);
they also completed more years of schooling (New Jersey site) (Salkind & Haskins,
1982). Other research that has followed children through “naturally occurring” changes
in family resources also has demonstrated within-child associations between family
income and behavioral problems. Children showed fewer externalizing problems such
as physical or verbal aggression during times when their families’ income was relatively
high compared to when it was relatively low, and this effect was particularly pronounced
for chronically poor families (Dearing, McCartney, & Taylor, 2006).
From another perspective, it might be noted that one recurrent and pervasive
socioemotional aspect of poverty—involving relatively lower “power,” in the broad
senses of “empowerment,” across a range of socioeconomic and other circumstances—
may itself detrimentally impact executive function. Such impairments associated with
lower social/interactional power have been found even when induced via relatively
transient and modest experimental manipulations in university students (Guinote,
2007; P. K. Smith et al., 2008). In university students (who otherwise might be gener-
ally characterized as a relatively “advantaged” group), across three different manipula-
tions of power, P. K. Smith and colleagues (2008) found impairments of executive
functioning in those with lower power, including impairments in processes of inhibit-
ing and updating, as well as planning. Performance deficits associated with lower
power emerged under quite different experimental manipulations, including semantic
priming of concepts of relative dominance versus subordination, assignment to an
evaluator versus evaluated role, and autobiographical recollection of situations involv-
ing power versus powerlessness. Furthermore, the impairments did not appear to
reflect differences in motivation. The groups reported putting similar amounts of
effort into the tasks and, more persuasively, performed similarly on a task that largely
continuously, rather than only intermittently, demanded inhibiting prepotent
responses, suggesting an increased likelihood of disruption of more difficult goal
maintenance under conditions of low power.
These findings also prompt the question of how much of the SES differences that
are observed relate to long-term versus immediately proximate effects in the testing
Making Br ain Paths to Agil e T h in k in g , Part 1 521
situations. Here we might recall the work of G. L. Cohen and colleagues (2006,
2009) on self-affirmation interventions to counteract the detrimental effects of
stereotype threat that demonstrated clear beneficial effects on the academic perfor-
mance of African American school children. (See the section on “Self-Affirmation and
Flexible Thinking” in Chapter 6; also compare with evidence reported by Sherman
et al., 2009, that self-affirmation reduced stress-related increases in epinephrine in
college students taking an important examination, with this effect most pronounced
in students who were most concerned about negative college evaluation; compare,
too, with the recent “social belongingness” intervention adopted by Walton & Cohen,
2011). Similarly, objective and immediately proximate effects of a given environment on
test performance might encompass aspects of natural versus urban environments.
Both actual walks and viewing pictures of natural scenes were found to improve
measures of working memory and attention compared to walking in, or viewing
pictures of, typical urban contexts (Berman et al., 2009; see the section on “Attention
Restoration Theory and Experiences of the Natural Environment” in the following
chapter).
Thus, although no one investigation or methodological approach can support
specific causal claims of a relation between the adverse physical and socioemotional
environmental conditions that characterize the lives of children, youth, and adults of
lower SES, and their tendency to obtain lower scores on assessments of executive,
memory, and attention function, the evidence to date clearly indicates that there are
multiple contributors. Furthermore, those contributors encompass factors beyond
SES disparities in any one domain such as health or nutrition alone (e.g., Farah et al.,
2008). Both the absence of multiple forms of positive environmental stimulation, and
the unfortunate and far too-frequent presence of stressful and harmful stimuli, add to
the burden and to the substantial human costs of poverty, and they contribute to
income and SES-related discrepancies in neurocognitive function and achievement.
Deep economic disparities may progressively undermine the capacity for creatively,
adaptively, and resiliently overcoming adversity, diminishing the mental agility of
those who, sadly, may need it most given the many sources of stress that poverty brings
in its wake.
Multidimensional Interventions in
the Community: Promising Beginnings
In this, the final section of this chapter, we will return to the other end of the develop-
mental spectrum and briefly consider innovative broadly based or “multimodal” inter-
ventions that have been undertaken to promote more extensive and more diverse
cognitive, social, and physical engagement in particularly older adults, and that have
evaluated how these interventions affect measures of health and cognitive function.
Two prominent examples of such interventions are the Experience Corps program and
the Senior Odyssey program, developed as a parallel to the “Odyssey of the Mind” pro-
gram aimed at younger age groups. (A third and highly innovative intervention, in
which older adults in a retirement home engaged in extensive theatrical training,
requiring a complex integration of multimodal, social, and emotional information, as
522 BRAIN AND ENVIRONMENT
well as a wide range of novel mental and physical activities, is reported by Noice &
Noice, 2009).
The first of these interventions, the Experience Corps program, is a volunteer
service in which older adults learn to help young elementary school children in school
settings to improve the child’s educational, social, and other capacities (Fried et al.,
2004; Glass et al., 2004). The program was established with four interlinked goals,
intended to increase the ongoing motivational, cognitive, physical, and social engage-
ment of older adults (see also E. C. Schneider et al., 2007). Specifically, the program
aimed to create a context in which older adults could become:
The initial trial of the Baltimore program involved 149 older adults, including many
individuals who were in a sociodemographically high-risk sample for cognitive decline
(for example, the mean age of the participants was nearly 70, and participants had an
average of more than two health conditions diagnosed by a physician, with about 70%
diagnosed with high blood pressure and some 25% with diabetes). A total of 21 per-
sons withdrew following the randomization, leaving 70 in the intervention group and
58 in the wait-list control group. Individuals in the intervention condition first
received training to enable them to engage in roles such as helping to build literacy
skills; they also took part in teams that met regularly for engaging in problem solving
and planning, and socializing. They then, over the course of many months, for an aver-
age of about 15 hours a week, helped children in the grades kindergarten to third
grade with their reading, and with their play and cooperative social interaction skills.
For the older adults, participation in the program, as assessed at 4- to 8-month
follow-up (Fried et al., 2004), was associated with increases in physical activity and
physical strength and decreases in the time spent watching television. Additionally,
consistent with other research showing that volunteering is associated with greater
social integration and increased social connections (e.g., A. H. S. Harris & Thoresen,
2005), the program led to improvements on measures of perceived social support.
Those in the intervention condition also showed improvements on two more formal
assessments of cognitive function (M. C. Carlson et al., 2008), including the inhibitory
control portion of the Trail Making Test (Part B, that requires alternation between
numbers vs. letters) and delayed memory recall of a complex abstract line drawing
that they had earlier copied (the Rey-Osterreith Complex Figure Test; Lezak, 1995).
These improvements were especially marked in the participants who were in the
lowest third of the distribution on the Trail Making Test at the outset of the study,
with baseline performance that was suggestive of cognitive impairment.
These promising findings suggest that multicomponential and “real-life” interven-
tions may be successful by “integrating the individual effects of increased cognitive,
social, and physical activity into daily life, thus allowing for large daily doses of
Making Br ain Paths to Agil e T h in k in g , Part 1 523
stimulating activity” (M. C. Carlson et al., 2008, p. 799; cf. Kramer et al., 2004).
A key aspect of the Experience Corps program entails potential conjoint effects on
motivation. Carlson and colleagues note:
Physical
Activity
Social
Activity
Figure 10.11. Hypothesized Causal Pathways of the Multimodality Experience Corps Program: Effects on Cognitive Health
and Functioning in Older Adults. Hypothesized causal pathways of the multimodality Experience Corps: Baltimore program effects on
cognitive health and functioning in older adults. IADL, instrumental activity of daily living. Reprinted from Carlson, M. C., Saczynski, J. S., Rebok,
G. W., Seeman, T., Glass, T. A., McGill, S., Tielsch, J., Frick, K. D., Hill, J., & Fried, L. P. (2008, p. 795), Exploring the effects of an “everyday” activity
program on executive function and memory in older adults: Experience Corps, The Gerontologist, 48, 793–801, with permission from Oxford
University Press. Copyright 2008, Oxford University Press.
Making Br ain Paths to Agil e T h in k in g , Part 1 525
Although the design and execution of this naturalistic experiment were not entirely
“tidy” (e.g., assignment was not completely random in that individuals in a retirement
community and couples were assigned to the same condition, and there was attrition
of nearly 25% from the experimental group), nonetheless, it is an important initial
step toward increasingly analytical assessment of the effects of multimodality and
non-laboratory-based interventions on cognition. As noted by one investigator:
The finding that neural stem cells […] persist in the adult brain
and give rise to new neurons throughout life has […] added a
completely new level of complexity to adult brain function.
—S. Jessberger & F. H. Gage (2008, p. 684)
The previous chapter has marshaled several sources of evidence that, taken together,
make a strong case for the key formative role of diverse types of cognitive, sensory-
motor, and social-cultural stimulation in preserving and enhancing mental flexibility.
Yet important limitations to the conclusions that can be drawn from such indirect
correlational and longitudinal studies also were noted. For instance, did individuals
who became taxi drivers in the London taxi driver study (Maguire et al., 2000)
preselect themselves—on the basis of their aptitude for navigation and ready acquisi-
tion of spatial maps—into this highly demanding spatial-navigational world? If so,
what factors, including the relative size or distribution of brain regions involved in
spatial navigation and memory, also correlated with such preselection? Although
additional observations, such as the correlation between the number of years of
taxi-driving experience and volume in the right posterior hippocampus, suggested
that it was the additional driving experience itself that led to a relative redistribution
of hippocampal gray matter in these individuals, an inferentially stronger foundation
for this causal conclusion would be obtained if the same or similar results were
526
Making Br ain Paths to Agil e T h in k in g , Part 2 527
(e.g., Joseph & Gallagher, 1980; Kempermann, Kuhn, & Gage, 1997; Kobayashi,
Ohashi, & Ando, 2002). Animals exposed to enriched compared to impoverished
environments also are quicker to learn tasks that require a reversal of a response that
was learned previously in a visual discrimination task (e.g., Doty, 1972; Krech et al.,
1962; compare with the earlier discussion of “Set Shifting and Reversal Learning” in
Chapter 8). For example, Milgram et al. (2005) found that aged beagle dogs given
behavioral enrichment demonstrated both improved discrimination learning and
reversal learning compared to controls that were not given enrichment (e.g., a novel
set of toys each week). Similarly, animals from enriched environments show an
advantage in other forms of response flexibility, such as that required for alternation
learning (Nyman, 1967).
Animals from enriched environments also demonstrate greater ability to transfer
their learning to new situations—likewise an important aspect of agile thinking.
One study (Morgan, 1973) found that although rats from enriched and impoverished
conditions did not differ in the rate at which they first learned to remove an obstacle
so as to be able to enter a food compartment, the enriched rats were more adept at
learning how to remove the obstacle in a different way from that learned initially. The
impoverished animals showed marked slowness in abandoning a strategy that was at
first successful (pulling a ball in a narrow alleyway toward the start box, so as to clear
a path to the goal box and to reward), but that was subsequently rendered no longer
effective by a change in the experimental apparatus (when, instead, the obstructing
ball could be removed only by pushing it toward the goal box).
Another study (Luchins & Forgus, 1955) found that animals from enriched environ-
ments were quicker than those from impoverished environments to abandon a longer
indirect path through a maze (and to food rewards) that, though previously forced, was
no longer necessary because the conditions necessitating the indirect path were
removed. Indeed, a number of animals from the impoverished environments contin-
ued to use the indirect route, which was nearly twice the distance as the direct route,
even after being forcibly shown that the direct path was now possible. These outcomes
again demonstrate an enhanced ability to adaptively alter behavior and previously
learned habits in animals from enriched compared with impoverished environments.2
These and other changes in adept problem-solving ability are paralleled by, and may
themselves partially reflect, many changes in brain function (e.g., M. C. Diamond,
Lindner, & Raymond, 1967). Sirevaag and Greenough (1987; 1991; A. M. Turner &
Greenough, 1985) conducted a comprehensive series of studies to analyze a wide
range of possible cortical synaptic, cellular, and vascular changes in rats raised in
enriched compared with control environments. Using light- and electron-microscope
techniques, these researchers demonstrated that enrichment experiences were associ-
ated with several significant and interrelated brain changes. Animals from enriched
environments showed a greater number of synapses per neuron (more than 20%
increase), enhanced dendrite length (approximately 10% increase), and greater vascu-
lar volume (approximately 50% increase) than did control animals. They also had
enhanced neuronal support and greater metabolic activity as indicated by higher
mitrochondrial volume, and by more astrocyte processes, especially after about
30 days of enrichment, with more prolonged enrichment perhaps also leading to an
increased number of astrocytes (Sirevaag & Greenough, 1991).
Making Br ain Paths to Agil e T h in k in g , Part 2 529
supragranular neurons of the occipital cortex was better preserved in the social condi-
tion, but that “exposure to isolation expedites segment shortening, segment loss, and
shifts in the basal dendritic tree that may occur in aging animals.” Mohammed and
colleagues (2002) placed rats that were 22 months of age into an enriched versus
standard environment. Enrichment was associated with increased dendritic spine
densities in each of three areas that were examined: the visual cortex, the hippocam-
pal formation (dentate gyrus), and the entorhinal cortex.
In other work, Kempermann and colleagues (2002) showed that, compared to older
mice housed under standard conditions, older mice housed under enriched conditions
for a sustained period of time showed enhanced performance on a Morris water maze.
Although the two groups did not differ on the very first trial, animals from enriched
environments found the submerged platform more quickly than did the control
animals on each of the subsequent trials, suggesting that they were more adaptive in
their exploration of the environment. The older animals from an enriched environ-
ment also were able to remain balanced on a rotating rod for almost twice as long as
the control animals.
Investigations that have sought to chart the occurrence of the generation of new
neurons (neurogenesis), particularly in the hippocampal dentate gyrus, as a result of
environmental enrichment have shown that, in older age, the baseline rate of adult
hippocampal neurogenesis is very low. However, changes in environmental stimula-
tion may—in relative terms—lead to a much more marked up-regulation of neurogen-
esis (Kempermann, Kuhn, & Gage, 1998; Segovia et al., 2006; see Fig. 11.1 for a
A B
Young adult Aged Experience-enriched aged
schematic depiction of the number of newborn granule cells in the young adult versus
aged adults, and experience-enriched aged adults). Kempermann, Gast, and Gage
(2002; see also Kempermann et al., 2004) found that mice exposed to environmen-
tally enriched living conditions beginning at “midlife” (between 10 months and 20
months of age) showed hippocampal neurogenesis that was nearly five times greater
than that shown by controls. Additional analyses suggested that this neurogenesis
reflected a shift in the distribution of newly formed cells, such that the number of
newly generated glial cells was reduced in the enriched animals. There was also some
evidence that enrichment decreased nonspecific age-dependent degeneration in the
dentate gyrus in that enriched animals showed reduced lipofuscin deposits, which are
a prominent sign of aging in the brain.
The precise function of the new (adult-generated) neurons is a topic of ongoing
debate (e.g., Lledo & Saghatelyan, 2005) though there are several features of the
neurogenesis that must be explained by any account. Prominent among these is the
observation that hippocampal neurogenesis appears to be found only in a quite specific
region—in the granule cell layer of the dentate gyrus, the quite narrow input struc-
ture to the hippocampus—where it is also known that representations and activity
patterns are extremely sparse. Therefore, as Kempermann observes, “adding new
neurons to this reduced network with its sparsely firing neurons might be a way to
economically optimize the projection into the hippocampus proper.” In addition
“adding neurons here might be a way to solve the so-called stability-plasticity dilemma,
which is particularly pressing at a network position where constantly new information
is flooding in and endangers the proper consolidation of the previously learned
contents” (Kempermann, 2008, p. 164).
The latter possibility also was considered by Bischofberger (2007), particularly in
relation to important evidence that the young granule cells show a temporally
restricted period of enhanced excitability compared to old granule cells. Using immu-
nohistochemical methods to visualize the recruitment of new neurons into the neural
circuits that support water maze learning in mice, Kee et al. (2007) found that as the
adult-generated cells became mature, it became increasingly likely that they would be
incorporated into circuits supporting spatial memory for the task. New neurons were
recruited into spatial memory networks by about 4 weeks, and by about 6–8 weeks
they were as much as twice as likely as were mature neurons to be recruited. This pref-
erential recruitment was most pronounced in the innermost portion of the dentate
gyrus. Figure 11.2 summarizes the time course of development of newly generated
granule cells in the adult hippocampus, from the initial stem cell, through neural
progenitors, to newly generated immature and finally mature neurons (see Kee et al.,
2007 and Bischofberger, 2007 for additional details).
Although there also is evidence that the new neurons are not essential to the
learning of all hippocampus-dependent tasks, including the water maze (e.g., Meshi
et al., 2006; Wojtowicz et al., 2008), reduced neurogenesis may be highly detrimental
to other tasks (e.g., contextual fear conditioning; Wojtowicz et al., 2008). Additionally,
Kee and colleagues suggest that already-existing granule cells might be sufficient to
support learning, though these memories might be less temporally specific (Aimone,
Wiles, & Gage, 2006) or more prone to interference (e.g., Becker, 2005; Wiskott,
Rasch, & Kempermann, 2006). As proposed by one researcher:
532 BRAIN AND ENVIRONMENT
Glutamate
Glutamate Glutamate
GABA GABA
GABA
GFAP
The enhanced plasticity of newly generated young granule cells might facili-
tate feature learning during exploration. As old granule cells show a higher
threshold for synaptic plasticity, the connectivity might become relatively
stable later on. As a consequence, mature neurons would be most sensitive to
features they learned when they were young. Adding new neurons could help
the network to achieve both stable analysis of “old” features as well as adap-
tation to new environments, finally supporting precise and distinct repre-
sentations of new memories throughout life. (Bischofberger, 2007, p. 275)
Making Br ain Paths to Agil e T h in k in g , Part 2 533
According to this account, the relevant mechanisms operate on both short- and
long-term time scales such that a very nonspecific broadly activated system (related to
physical activity) “sets the stage on which the particular cognitive stimuli that recruit
individual neurons might act” (Kempermann, 2008, p. 165). Thus, activity helps to
preserve the capability for long-term levels of cell-based plasticity by maintaining
adult neurogenesis in an activated state.
Figure 11.3 graphically illustrates these proposed interactions between environ-
mental stimulation, continued neurogenesis in the hippocampus during adulthood,
and adaptive responding to novelty and challenge—or the “neurogenic reserve
hypothesis.” The uppermost panels of the figure show the contrasting effects of high
versus low levels of adult hippocampal neurogenesis on how an organism responds to
novel information. The animal with a high level of adult neurogenesis, shown in Panel
(A), can readily “adapt to the new situation and learn the distinguishing differences,
thereby expanding its cognitive map (i.e., the representation of the environment)
without catastrophic interference between novel and previously learned information.”
In contrast, the animal with low adult hippocampal neurogenesis, shown in Panel (B),
is unable to realize such “adjustment and optimization of the mossy fiber connection”
and the novel information leads to interference with previously learned information.
The middle and lowermost panels contrast the longer term effects of an organism that
has comparatively few experiences of novelty, shown in Panel (C), with an organism
that very frequently encounters novelty, shown in Panel (D). As characterized by
Kempermann:
(a) Adult neurogenesis (b) Lack of adult neurogenesis
allows adaptation to new experiences results in reduced functional plasticity
Young-adult High levels Young-adult Low levels
of adult of adult
neurogenesis neurogenesis
(c) Lack of exposure and training in younger age leads to reduced cellular
and functional plasticity with increasing age
High levels Strong Old Low levels
Young-adult of adult age-related of adult
neurogenesis decrease neurogenesis
No
reserve
(d) Exposure and training in younger age builds a neurogenic reserve for cellular
and functional plasticity in the aging hippocampus
High levels Reduced Old High levels
Young-adult of adult age-related of adult
neurogenesis decrease neurogenesis
Neuro-
genic
reserve
534
Making Br ain Paths to Agil e T h in k in g , Part 2 535
On longer timescales, the fact comes into play that the learning experience
itself (as well as locomotion) as the means of navigation in the physical (and
thus cognitive) space affects the regulation of adult neurogenesis. If there is a
lack of stimuli, represented by the prolonged exposure to the same environ-
ment, adult neurogenesis decreases and the potential for recruiting the nec-
essary new neurons in times of computational need is reduced. No reserve
has been built. […] By contrast, if the individual experiences a high level of
complexity and novelty (i.e. has to physically navigate in a complex and chang-
ing world), precursor cell activity remains high, a neurogenic reserve is built
and the hippocampus can still plastically adopt to very novel situations that
are experienced for the first time in older age. (Kempermann, 2008, p. 166)
Critically, from this perspective, and in terms of the iCASA framework, increasing
environmental complexity can be seen as increased understanding of and differentia-
tion between multiple different “exemplars” of a given sort of stimulus, or experience.
Exposure to many different contexts or instances—of objects, events, ideas, places,
and so on—allows both maintenance of earlier information and accommodation of
(learning of) new information. In contrast, exposure to only one or a few contexts or
instances leads to decreased adaptability, and potentially substantial interference
(failure to learn, or forgetting).
An interesting prediction that follows from this account relates to the relative ini-
tial amounts of exposure to different contexts or instances that an organism has expe-
rienced. In particular, if an animal has experienced a wide variety of different contexts
or instances across a period of time, then exposure to yet another context or instance
from the same broad class or classes might be less “novel” than it would be to a more
naïve animal—with consequent differences in the implications for neurogenesis:
If the neurogenic reserve hypothesis is true, one will, for example, also find
that in an old animal that has seen very many environments, the regulatory
effect of yet another new environment on adult neurogenesis will be lower
than in a naïve animal. The relationship between adult neurogenesis and
levels of adult neurogenesis might consequently become complicated: it is
conceivable that despite a positive correlation between adult neurogenesis
and cognitive performance on certain hippocampus-dependent functional
domains, exceptionally well adapted animals might even have less adult
neurogenesis than those for which there are still challenges. (Kempermann,
2008, p. 167)
that very frequently encounters novelty, shown in Panel D, and that consequently has
both neurogenic reserve and adaptive flexibility in accommodating further new
experiences. See text for additional details. Figure adapted from G. Kempermann
(2008, p. 166), The neurogenic reserve hypothesis: What is adult hippocampal
neurogenesis good for? Trends in Neurosciences, 31, 163–169, with permission from Elsevier.
Copyright 2008, Elsevier. Note: See the insert for a full-color version of this image.
536 BRAIN AND ENVIRONMENT
Less speculatively, other evidence clearly suggests that there are some limitations
on plasticity in older animals. For instance, the longer term enhancement from
enrichment (increased population spiking over baseline values in hippocampal
dentate gyrus cells) was found to decay more rapidly in older rats compared to younger
animals (Sharp, Barnes, & McNaughten, 1987). Furthermore, there may be important
differences in the speed with which brain changes occur. Periadolescent rats, for exam-
ple, appear to have both particularly plastic brains, and to be especially likely to show
rapid brain changes, in part because they exhibit high levels of play and exploration
(Ferchmin & Eterovic, 1986).
The precise way that the brain changes in response to enriched experience also
depends on the age at which enrichment occurs. One study contrasted brain changes
shown in rats that were placed into enriched “condominiums” in young adulthood, as
juveniles (directly after weaning), or in old age (senescence). Both the young adult
and older animals showed brain changes similar to those that have been reported
previously, including a large increase in dendritic length and increased dendritic
spine density compared to that shown by age-matched control rats housed in regular
cages. In contrast, this was not observed in the juvenile animals. Juveniles showed
only an increase in dendritic length or branching—and a decrease (rather than
increase) in dendritic spine density (Kolb, Forgie, Gibb, Gorny, & Rowntree, 1998).3
Thus, although animals at all ages showed changes in dendritic structure as a conse-
quence of environmental enrichment, enrichment may have qualitatively (and not
only quantitatively) different effects depending on the age at which the increased
stimulation occurs.
Age differences also often alter the ways in which the animals actively explore their
environment and interact with objects. Kolb et al. (1998) report that whereas the
young and middle-aged rats in their experiments explored the entire complex of their
enriched condominiums, some of the older rats mostly confined themselves to the
ground level. These older animals essentially ignored the upper levels of the structure,
either because of reduced motoric abilities or because of reduced motivation to explore.
Interestingly, however, even within the older group of animals, animals that did more
extensively explore all levels (“climbers”) had larger brains than did the animals that
explored less extensively (“nonclimbers”).
Enriched environments also may be seen as providing opportunities for variable or
novel behavior. As we saw in Chapter 5 (throughout the section on “Learning to
Vary versus Learning to Repeat”), directly reinforcing variable behavior, rather than
habitual or repetitive actions, often enhances problem solving in new situations.
For instance, rats that were earlier directly reinforced for interacting with various new
objects in many different ways, subsequently, in a novel context involving never-
before presented objects, showed significantly greater problem-solving skills. The ani-
mals previously reinforced for varying their behavior were significantly more efficient
in retrieving hidden morsels of food in the new objects and new environment than
were control animals that were reinforced equally often, but in a manner that was
unconnected to their activity (“yoked controls,” Neuringer, 2004).4
A question that one might ask is whether physical interaction with the novel
objects and environment is critical for the beneficial effects to be observed. Is direct
Making Br ain Paths to Agil e T h in k in g , Part 2 537
to their water stations. In contrast, rats in the impoverished condition merely needed
to travel across an empty box between the food and water stations. Even under these
tightly controlled conditions, beneficial brain effects similar to those found in many
other studies of environmental enrichment were observed.
Other research has examined the effects of specific forms of sensory or motor
training on the brain processes of animals. In a classic study, Chang and Greenough
(1982) restricted the visual input of rats during maze training to only one cerebral
hemisphere by using an eye patch and severing the rats’ corpus callosum so as to
largely preclude communication of visual information between the cerebral hemi-
spheres. They found that the trained cerebral hemisphere had more extensive dendrite
branching than did the nontrained hemisphere, showing that “the brain effects are
localized in a region involved in sensory aspects of the training experience” (p. 289).
In other research, it has been shown that environmental enrichment can counteract
the detrimental effects of a previous lack of visually driven activity, and enable the
development of normal visual acuity maturation in dark-reared rodents (Bartoletti
et al., 2004). Monocular deprivation in 50-day-old rats resulted in a significant
shift in the fraction of cells in the visual cortex that responded to the deprived eye for
animals that were dark-reared under standard conditions, but no such shift in the
ocular dominance distribution was found for dark-reared animals given environmen-
tal enrichment.
This finding was further supported by evidence that for the environmentally
enriched animals, but not the standard-reared animals, there was largely normal devel-
opment of visual connections and therefore also resistance to reorganization via mon-
ocular deprivation (the density of neurons in the visual cortex that were surrounded
by perineuronal nets was normal in layer 4, and nearly normal in layers 2/3 and 5/6).
In addition, electrophysiological estimates of visual acuity using visual evoked poten-
tials demonstrated impaired visual acuity in dark-reared standard-housed animals
(at postnatal day 60) but normal visual acuity in the dark-reared animals raised under
environmentally enriched conditions. Thus, environmental enrichment promoted the
development of visual connections and enabled normal neuronal development for
these dark-reared animals (see also Cancedda et al., 2004, and Sale et al., 2009).
Changes in specific behavioral patterns, such as the use of a particular forelimb for
a reaching task, also have been found to selectively alter the density of synaptic
branching in only one brain region of an individual animal. This points to quite
specific, experientially related alterations in the pattern of brain connectivity even
within a single animal (e.g., Greenough, Larson, & Withers, 1985; Kolb et al., 1998).
Together, these studies also demonstrate that it is not only extreme variations in envi-
ronmental complexity and stimulation that are important: Relatively more subtle and
narrow changes in daily learning and stimulation likewise appear to have significant
effects on both the brain and adaptive (flexible) behavior.
In summary, there is convincing evidence that enriched environments lead animals
to show more flexibly adaptive thinking and that these changes are accompanied by
diverse and pervasive brain changes. Facilitated learning and problem-solving in new
situations, enhanced learning of “reversals,” and a readier transfer of learned skills to
novel situations are among the adaptive behaviors and cognitions shown by animals
from enriched compared to impoverished environments.
Making Br ain Paths to Agil e T h in k in g , Part 2 539
This was essentially the pattern of outcomes that was observed. For both groups,
brain regions that were activated during the initial learning of the task (e.g., bilateral
primary sensorimotor cortex, basal ganglia, and parietal regions) showed decreased
activity as the sequences became increasingly well learned by pianists and the non-
pianists alike. However, several brain regions showed increased activity (in both
magnitude and extent) for only the group with expertise. These latter regions were
primarily in a right-lateralized network of prefrontal, motor, and cingulate regions,
suggesting that prior motor-related training led to the involvement of a broader set of
regions for task performance.
This study does not allow a definitive determination of the mechanisms leading to
these different effects. Nonetheless, Landau and D’Esposito (2006) argue that, given
that the observed decreases in brain activation common to the two groups were shown
rapidly, within a single experimental session and within a matter of only minutes or
hours, they likely reflect either changes in synaptic efficiency, or recruitment of
existing networks. In contrast, the slow changes typical of the acquisition of longer
term expertise, most often occurring over weeks or years, might arise through synap-
togenesis—that is, modifications in axonal and dendritic structure—involving
reward-motivated learning and neurochemical interactions (e.g., release of acetyl-
choline, noradrenaline, and dopamine) between basal ganglia/midbrain regions and
somatosensory cortex. Notably, Landau and D’Esposito also explicitly point to the
relevance of these findings to interpretive issues relating to “neural efficiency,” setting
the evidence for both experience-related reductions and experience-related increases
in brain activation that were shown by the pianists against an overly simplistic view
according to which optimized neural processing is necessarily reflected in reduced
activity. Rather, they propose that “an optimized motor system is capable of greater
flexibility and adaptability, depending on the demands of the task. This may mean
reduced activity in the case of simple and repetitive motor tasks, or it may mean
recruiting an extensive network of primary and multimodal regions during perfor-
mance of complex tasks” (Landau & D’Esposito, 2006, p. 257).
These findings point to the interlinked roles of behavioral and neural plasticity in
the learning of serial reaction time sequences, acquired within a single session. What
about more complex visual-spatial-motor tasks, learned over additional sessions, or
periods of weeks or months, or tasks directly involving more cognitive or representa-
tional functions?
Learning-induced cortical plasticity, even at the structural level of the brain, was
recently demonstrated in humans by examining the effects of first acquiring and then
no longer maintaining a skill that relatively few of us likely possess: that of juggling
(Draganski, Gaser, Busch, Schuierer, Bogdahn, & May, 2004). Participants were first
given a brain scan when all of them were naïve to juggling. This brain scan focused not
on the areas of the brain that were activated by performing a task (functional MRI) but,
instead, was a very high-quality scan of the anatomical structure of the brain (MRI).
After this initial brain scan, one-half of the participants were given 3 months to
practice juggling. They were asked to practice until they became proficient at a classic
three-ball cascade juggling routine. When they had become skilled at this routine—as
evidenced by the ability to sustain juggling with three balls for at least 60 seconds—
they were given a second MRI brain scan. This scan provided a second high-quality
Making Br ain Paths to Agil e T h in k in g , Part 2 541
image of the anatomical structure of their brains that could be compared to the
first scan.
To compare the first versus second scans, and to examine the whole brain for
changes in anatomical structure in the jugglers versus nonjugglers, the researchers
used the technique of voxel-based morphometry (e.g., Ashburner & Friston, 2000).
This method, which was also used in the study of London taxi drivers, discussed in
the previous chapter, allowed the researchers to identify regions of brain gray matter
concentration that differed significantly between the newly proficient jugglers versus
the naïve juggler groups.
These analyses revealed that individuals who had newly acquired the skill of
juggling showed a significantly increased concentration of gray matter in a motion-
sensitive area of midtemporal cortex (hMT/V5) in both the right and left cerebral
hemisphere, and also an increase of gray matter concentration in the left posterior
intraparietal sulcus. The latter region is involved in visual-spatial attention and spatial
transformation. It has been associated with attentional modulation of visual search
(Donner, Kettermann, Diesch, Ostendorf, Villringer, & Brandt, 2000) and with smooth
eye movement pursuit of target objects in situations where the object can no longer be
seen (Lencer et al., 2004). There were no changes in gray matter of the nonjugglers
over the same period, demonstrating that the changes were specific to the engage-
ment in training of this complex skill.
These findings both further support, and significantly extend, the conclusions
based on the London taxi driver study. A key strength of this study is the experimental
assignment of participants to the practiced versus naïve juggling conditions.
Experimental assignment to the experimental versus control conditions substantially
undermines the feasibility of an alternative account that would attribute the findings
to a form of “self-selection” into a profession or area of expertise for which (possibly
because of the structure of one’s brain) one already has a special aptitude. The study
also demonstrates that even relatively short-term alterations in our experience—
experiential changes undertaken over the course of months—can lead not only to
alterations in the way that the brain processes information but also may change brain
structure (the distribution of gray matter concentration).
The juggling study involved a further manipulation that provides additional evi-
dential support for the ongoing causal role of experiential input in the brain changes
observed. The now proficient jugglers were asked to abstain from juggling for a further
3 months and were then given yet another detailed structural brain scan. At the time
of this third scan most of the participants in the juggling condition were no longer
proficient in the three-ball cascade routine—and the previously identified region-spe-
cific gray matter concentration changes in motion-sensitive areas of the brain were
significantly attenuated. Thus, as the participants progressively lost facility in their
new skill of juggling through lack of practice, the specific brain changes that emerged
during the learning of that skill likewise were progressively lost.
A more recent investigation using an experimental design paralleling that used in
Draganski et al. (2004) replicated and extended these findings but with juggling-naïve
healthy older adults (Boyke, Driemeyer, Gaser, Büchel, & May, 2008). Although
older adults did not reach the same level of juggling proficiency as shown by younger
adults, those older adults that were able to learn the three-ball cascade, like their
542 BRAIN AND ENVIRONMENT
examined the effects of prolonged practice on tasks that require working memory—
that is, our ability to keep in mind, and consciously use and manipulate, several differ-
ent pieces of information at a time.
Working memory is an important building block that we rely on in solving
problems and engaging in creative reasoning of all forms (e.g., Carpenter, Just, &
Shell, 1990). Larger working memory capacity is important in being able to keep track
of “where we are” as we work through a problem, particularly as we iteratively gener-
ate subgoals, mentally take note of what we find as we accomplish them, and then set
new subgoals. Working memory capacity positively correlates with performance on
multistage puzzles (e.g., a complex planning task known as the Tower of Hanoi) and
on tasks such as the completion of novel visual-spatial series (e.g., progressive matri-
ces). It has been argued that positive correlations between working memory and rea-
soning derive from a similar capacity limit relating to the ability to form and preserve
bindings between elements in memory, with working memory limited to approxi-
mately three to four chunks (e.g., Olsson & Poom, 2005) and reasoning similarly lim-
ited to relations between up to four variables (Halford, Cowan, & Andrews, 2007).
Although an individual’s working memory capacity traditionally has been viewed
as constant, Olesen et al. (2004) demonstrated that individuals can, through training,
extend their working memory capacity (see also note 4). In their study, healthy adults
practiced three visual-spatial working memory tasks each day for 5 weeks. They were
presented several successive target items displayed in a particular location of a grid
(Grid, Grid rotation, and 3D Grid) and then required to recall each of the target
locations shown, in the correct sequence.
Working memory training began on the first day at a fixed level (level 2, a sequence
of two cues) for all tasks, with difficulty adjusted to performance. Then, on each
successive training day, the starting level of difficulty corresponded to the level that
had been achieved on the preceding day. To examine the effects of this extensive train-
ing on brain activity, the participants were given brain scans while performing a simi-
lar working memory task (functional MRI), and a control task, on five different
occasions: day 1, and then days 2, 4, 8, and 23 of the working memory training.
The results showed that the training sessions led to continuous improvements in
working memory on each of the three tasks. Across the five scanning days, the level of
accuracy, combining across both easier sequences with few items and more difficult
sequences with many items, significantly increased from nearly 30% to nearly 45%.
Furthermore, these increases in accuracy were accompanied by a significant decrease
in the amount of time required for responding.
Training also was associated with improvements on several neuropsychological
tests that were not directly trained. The tests included a different measure of visual-
spatial working memory (a Span board task), a measure of verbal working memory
(digit span), and a measure of response inhibition (the Stroop color-word task, mea-
suring the individual’s time to name the ink color of words that themselves designated
conflicting color names, such as the word “red” printed in green ink). However, com-
pared with the test-retest improvement shown by a control group, only the improve-
ment in the latter task reached statistical significance.
Several other studies, however, have more strongly supported the generalization of
the benefits of working memory training to at least some nontrained tasks (Buschkuehl
544 BRAIN AND ENVIRONMENT
et al., 2008; Klingberg, Forssberg, & Westerberg, 2002; Klingberg et al., 2005; S.-C.
Li et al., 2008), particularly in young adults (Dahlin et al., 2008) including, most nota-
bly, a measure of fluid intelligence (Jaeggi, Buschkuehl, Jonides, & Perrig, 2008).
In the latter study, younger adults were trained on a combined auditory and spatial
working memory task for up to 19 days, with the level of difficulty of the task
(the n-back task) successively adapted to their level of performance across the training
sessions. The trained group demonstrated an average performance increase of 0.65
standard deviations on a visual-spatial fluid reasoning task and this gain significantly
exceeded that found for a control group simply tested at the beginning and again at
the end of the experiment.5
Analyses of the brain imaging data collected by Olesen et al. (2004) showed that the
working memory training benefits that they observed were accompanied by two dis-
tinct changes in patterns of brain activity across the 5 weeks. On the one hand, one set
of brain regions showed increases in activity as a result of training. Increased brain
activity was shown in superior and inferior parietal cortex and middle frontal cortex, as
well as regions deep inside the brain in the nuclei in the basal ganglia (caudate nucleus)
and thalamus (pulvinar). On the other hand, another set of regions showed decreased
activity with training. Regions that showed training-related decreases in activity
included the anterior cingulate sulcus, postcentral gyrus, and inferior frontal sulcus.
Many studies have shown decreases in activation with repeated practice of a task or
with repeated presentations of stimuli such as words or objects (see, for example,
Grill-Spector, Henson, & Martin, 2006; Henson, 2003, for review). This suggests that
processing has somehow become more efficient with practice. However, the working
memory trials differed in an important way from many earlier studies involving
repeated presentations of stimuli.
Training or repetition in the earlier studies allowed, and probably even encouraged,
automatization of responding because the items were repeated multiple times. Indeed,
such automatization was shown in measures of stereotyped responding or stereotypy.
For example, in a “verb generation” task that required participants to provide verbs
that might go with presented nouns (e.g., dog–bark), participants repeatedly provided
the same verbs each time a given noun was presented (e.g., dog–bark) even though a
large number of alternative responses were possible (e.g., dog–walk, dog–wag,
dog–swim, dog–sleep). Across several experiments, involving both verb generation and
a similar type of word generation task, and using both visual and auditory presenta-
tion of stimuli, we found average rates of response stereotypy between 75% and 87%.
Indeed, individual participants sometimes gave stereotyped responses for more than
95% of the items (Buckner, Koutstaal, Schacter, & Rosen, 2000). By contrast, in the
working memory task used by Olesen et al. (2004), the stimuli were unique to each
trial, and the ongoing demand to keep new information “on line,” involving the active
maintenance of the current to-be-remembered set of target locations and sequence,
would act to prevent automatization.
Previous research has shown that the amplitude of the activation in a network of
regions in frontal and parietal cortex correlates with success on working memory
tasks. For example, successful recall of the to-be-remembered targets on any given
working memory trial was associated with greater activity in the frontal-parietal
cortex during the delay interval between the presentation of the to-be-remembered
Making Br ain Paths to Agil e T h in k in g , Part 2 545
sequence and the signal to recall the sequence (Pessoa, Gutierrez, Bandettini, &
Ungerleider, 2002). These findings also are consistent with research in primates, using
recording from single cells during working memory tasks, which have demonstrated
that there are neurons that show a sustained and stimulus-specific response during
the delay period, between presentation of the target and the cue to recall. As we saw in
Chapter 10, such neurons are found in prefrontal cortex but they may also, depending
on the task, be observed in inferior temporal cortex (for visual patterns or color
stimuli), the parietal cortex (for visual-spatial stimuli), and the premotor cortex
(for specific motor responses; see Pessoa et al., 2002 for review).
Nonetheless, there was also suggestive evidence, in the study by Olesen and
colleagues (2004) that, even with stimuli that were unique on each trial and that
required constant online maintenance and updating, decreases in the brain activity
involved in working memory might occur in some brain regions, particularly if the
training was extended across an even longer period of time. In the middle frontal gyrus
and superior parietal cortex the initial increases in brain activity shown in the first 4
weeks appeared likely to be followed by decreases or perhaps asymptotic levels of activ-
ity if training were continued beyond the fifth week (Olesen et al., 2004, Figure 3).
These latter findings are consistent with recent reviews arguing that there are multiple
ways in which brain activation might be affected by repeated performance of an activity
(Jonides, 2004; Kelly & Garavan, 2005; see also Dahlin et al., 2009). More specifically,
as noted earlier in connection with the findings for pianists versus nonpianists learning
serial response time sequences, it may be that comparatively fast learning, involving a
high level of repetition and automatization of performance, is associated with decreases
in activity within a given network of regions (e.g., Floyer-Lea & Matthews, 2004),
whereas slow learning, involving less repetition and the development of strategies for
task performance, is (also) associated with recruitment of additional regions as the task
is learned (e.g., Landau & D’Esposito, 2006; Olesen et al., 2004).
The key point from our current perspective, however, is that both behavioral
improvements, and systematically correlated changes in brain activity, were demon-
strated in conjunction with increased practice at a highly complex, not readily auto-
mated, working memory task. The task demanded flexible, ongoing updating and
revision of the individual’s goals and the mental representations that they were main-
taining in mind across time. The results thus provided clear initial evidence of train-
ing-induced plasticity in both brain and behavior for a complex cognitive task closely
associated with mental agility.
A more recent investigation, similarly involving multimodal working memory
training over a 5-week period in young adults, but using combined behavioral train-
ing, fMRI, and positron emission tomography, has begun to illuminate the biochemi-
cal bases of these effects (McNab et al., 2009). Using a paradigm based on the earlier
work of both Klingberg et al. (2002) and Olesen et al. (2004), McNab and colleagues
(2009) showed that training-induced improvements in working memory capacity
were significantly correlated with changes in the density of cortical dopamine (D1)
receptors. Although the relation between working memory performance and
dopamine binding potential also involved a curvilinear (inverted-U) component,
within the ranges investigated, there was a significant negative correlation between
D1 binding potential and working memory performance. Reductions in D1 binding
546 BRAIN AND ENVIRONMENT
potential were associated with increased working memory capacity in four out
of five independently determined regions of interest: right and left posterior regions
of parietal, temporal, and occipital cortices, a right dorsolateral prefrontal region,
including the right middle frontal gyrus and right superior frontal gyrus, and a right
ventrolateral prefrontal region, including the right inferior frontal gyrus. The findings
were specific in that no corresponding changes as a function of changes in working
memory capacity were found for the D2 dopamine receptor system. Together, these
outcomes attest to the “high level of plasticity of the neuronal system defined by
cortical D1 receptors” in healthy adult volunteers and “the reciprocal interplay between
behavior and the underlying brain biochemistry” (McNab et al., 2009, p. 802).
Other recent work has further begun to illuminate the effects of training in
working memory on white matter connectivity. Conceptually mirroring the findings
that Scholz et al. (2009) obtained for the juggling training task, using the technique of
diffusion tensor imaging, Takeuchi et al. (2010), demonstrated changes in white
matter microstructure in regions near left intraparietal sulcus from pretraining to
posttraining of working memory. These white matter changes (assessed by voxel-
based analysis of fractional anisotropy) were further found to be significantly corre-
lated with the total amount of training participants completed on the three different
challenging working memory paradigms over a course of about 2 months (range of
training between about 50 and 190 total sessions, with a mean of approximately 40
sessions for each of the three types of working memory training tasks).
Collectively, these and other studies6 demonstrate a simple but remarkable fact:
Throughout our lives we are flexibly tuning and adjusting the visual, cognitive, and
motor skills that we have and the discriminations that we can make, and our remark-
ably plastic brain is likewise changing as it adjusts to enable and support those skills.
What we do and what we think about—including the extent to which our thinking
involves a healthy exercising and stretching of our capabilities—changes not only
what we know and how we can use that knowledge, but also our brain, and precisely
how it can then further work with (store, connect, and use) that knowledge. Neither
our on-line ability to hold and manipulate multiple items or relations, nor our related
capacity to flexibly solve novel problems, is necessarily fixed. These capacities are, to
an extent that is not yet fully charted, malleable and subject to significant improve-
ment through training efforts that are—from the perspective of a lifetime—really
quite brief, a matter of weeks or months rather than years.
E X E R C I S I N G O U R B O D I E S TO E N H A N C E O U R M I N D S :
E X P E R I M E N TA L E V I D E N C E L I N K I N G P H Y S I C A L A N D
C A R D I O VA S C U L A R F I T N E S S TO C O G N I T I V E P E R F O R M A N C E
In Chapter 10, we considered evidence from a number of longitudinal and epidemio-
logical studies that pointed to the beneficial effects of regular physical exercise and
maintaining cardiovascular fitness on cognitive functioning. A growing number of
experimental studies have more firmly grounded this conclusion using random assign-
ment of participants to fitness training versus control conditions. A meta-analysis of
18 longitudinal studies that used experimental designs to examine the relation
between physical activity and exercise on cognitive functioning in older adults between
Making Br ain Paths to Agil e T h in k in g , Part 2 547
anterior cingulate cortex, a region associated with response conflict. Very similar
neuroimaging results were obtained by these researchers in an earlier cross-sectional
investigation, comparing individuals who entered the study with comparatively high
levels of aerobic fitness with those who were relatively less aerobically fit.
In follow-up work, Colcombe et al. (2006) examined possible structural (gray or
white matter) changes in the two randomly assigned groups from the Colcombe et al.
(2004) study using the technique of voxel-based morphometry. These analyses
showed that, for older adults in the aerobic fitness group but not for those in the
nonaerobic group, there were significant increases in gray matter volume in the fron-
tal cortex (anterior cingulate cortex/supplementary motor cortex and right inferior
frontal gyrus) and in temporal cortex (left superior temporal gyrus). The aerobic
fitness group additionally showed increases in the volume of anterior white matter
between the initial (Time 1) and the final (Time 2) scans.
Also using MRI measures, Pereira et al. (2007) reported that young to middle-aged
individuals (mean age of 33 years, range from 21–45 years) who engaged in a 3-month
aerobic exercise program showed increases in cerebral blood volume in the dentate
gyrus of the hippocampus. (Modest but not statistically significant increases also were
observed in entorhinal cortex.) These increases in cerebral blood volume were corre-
lated both with a measure of cardio-respiratory fitness (peak oxygen consumption)
and with cognitive measures of verbal learning and memory (a modified version of the
Auditory Learning Test). Notably, these researchers also earlier demonstrated, in
research with mice, that exercise had a selective effect on cerebral blood volume in the
dentate gyrus (with a trend for such an effect in entorhinal cortex), and that exercise-
induced changes in cerebral blood volume in the dentate gyrus in mice correlated with
postmortem measurements of neurogenesis. Additionally, they demonstrated that if
neurogenesis in the dentate gyrus was prevented, through the use of an x-irradiation
procedure, then the exercise-induced cerebral blood volume effect was likewise
blocked. In contrast, in a control group of mice, given a “sham” procedure without the
x-irradiation and for which neurogenesis thus remained possible, the cerebral blood
volume effect was again observed.
The mechanisms underlying the changes in frontal and parietal regions reported by
Colcombe and colleagues (2004, 2006) remain to be determined. However, work from
animal models suggests several possible, not necessarily mutually exclusive, possibili-
ties. Perhaps most likely are increases in brain-derived neurotrophic factor (BDNF)
and other nerve growth factors that, in rats, have been shown to lead to an increase in
the number of synapses, capillaries, and cell bodies. In particular, Vaynman and
colleagues (2004) demonstrated that, in rats, voluntary exercise increased both an
important intermediary in gene expression (mRNA) and BDNF in several regions,
including the hippocampus, cerebellum, and frontal cortex and—furthermore—that
interfering with BDNF (by blocking the binding of BDNF to its receptor) also
eliminated the behavioral benefits of exercise as shown on a water maze task.7 As
observed by Colcombe et al. (2004, p. 3320), “One possibility, then, is that increases in
cardiovascular fitness increases the number of interconnections (synapses) in frontal
and parietal gray matter, allowing for greater systematic recruitment of these areas
under higher cognitive load.” Other possibilities include increases in blood supply to
these regions or positive cholinergic effects.
Making Br ain Paths to Agil e T h in k in g , Part 2 549
were conducted over a 10-week period, with 5 weeks for figural relations training
and 5 weeks for induction training.
To evaluate the effects of the training sessions, a large set of eight different tests
was administered to all participants at the beginning and end of the 10-week period.
These tests sampled a wide range of types of abilities, including the same fundamental
abilities that were the focus of training (figural relations and induction, measured
using standardized tests), some that were similar to those abilities, and some that
were relatively different from those abilities (measures of perceptual speed and
vocabulary). This allowed determination of the degree to which any training benefits
that were observed were highly specific, that is, shown only on tasks that required
the same or highly similar procedures as those that were part of the training sessions
(“near transfer” tests), or were more broad improvements that were quite generally
shown even on tasks that did not require procedures like those that were trained
(“far transfer” tests).
Training significantly improved older adults’ performance accuracy on tasks
requiring on-the-spot thinking that were similar to those that had been trained on
(near-transfer tests; see also McArdle & Prindle, 2008). This increase in accuracy did
not reflect changes in the number of items that were attempted: The number of items
attempted was essentially identical in the experimental and control groups for the
four near-transfer tests, indicating that the training did not simply alter readiness or
willingness to try to solve the problems. Deliberate practice also enhanced older adults’
performance on the near-transfer tasks regardless of the degree of difficulty of the
problem.
Although extremely encouraging, and an “existence proof” for the beneficial effects
of deliberately “exercising the mind” for agile thinking in types of problems similar to
those that were practiced, several cautions in interpreting these results are necessary.
First, the study only examined training effects in older adults who were comparatively
healthy and well educated. It cannot be concluded that similar training benefits neces-
sarily would be shown in less healthy individuals (for example, those in the early stages
of dementia).8 It also is not possible to draw any conclusions about the relative ability
of older, compared with younger, individuals to benefit from training on fluid intelli-
gence tests. Only older individuals were tested, so it simply is unknown to what extent
younger individuals also might show training-related improvements, or whether or
not such improvements would be of a similar magnitude to those shown in the older
population. Finally, it is important to consider the amount of training: only 5 weeks
for each task. This is much briefer, and much less intense, than the years of deliberate
practice (Ericsson & Lehmann, 1996) undertaken by individuals who achieve high
levels of expertise in domains such as music or dance.
Closely related to this point is the question of the durability of the benefits
observed—do the benefits persist past the training period and, if so, for how long?
A partial answer to this question is provided by the results of three follow-up tests
that were administered 1 week, 1 month, and 6 months following the training. These
tests still showed improvement at 1 week; however, by 6 months, performance was
only very slightly and not reliably better than at pretest. Nonetheless, here, again a
comparison to research findings and detailed observations on deliberate practice are
informative: Among expert performers, deliberate practice is not simply abruptly
Making Br ain Paths to Agil e T h in k in g , Part 2 551
stopped once some level of achievement is reached, but rather is continued, at very
regular intervals, across years and years (not weeks or months).9
Additionally, other studies have provided evidence for benefits from direct training
in strategy application to specifically improve reasoning ability, such as training in
using rules to identify patterns (e.g., repeats of a pattern, or skips) in inductive reason-
ing tasks (Saczynski, Willis, & Schaie, 2002). The large-scale randomized controlled
single blind investigation known as the “ACTIVE” (“Advanced Cognitive Training for
Independent and Vital Elderly”) study found longer term maintenance of training ben-
efits on reasoning ability across periods as long as 2 years (Ball et al., 2002) and extend-
ing out to 5 years (Willis et al., 2006). Reasoning task training was further found to
enhance self-reported everyday living skills at 5-year follow-up (Willis et al., 2006).
Training in metacognitive strategies such as self-monitoring and self-testing, may
also prove beneficial, at least for participants who do not spontaneously or regularly
engage in such strategies, particularly as they can, in principle, be applied to any new
learning or performance task (Dunlosky et al., 2003; 2007). Results have further
shown that allowing participants to choose memory encoding strategies from among
a number of different but potentially effective instructed approaches may be more
beneficial for both immediate performance and transfer than requiring a specific
strategy (Lustig & Flegal, 2008). The latter researchers concluded that “manipulations
that encourage older adults to increase proactive control and deep encoding but that
allow flexibility in the method of doing so are the most likely to promote successful
training and transfer” (Lustig & Flegal, 2008, p. 763). A review of far transfer effects
in older individuals using strategy training versus extended practice approaches is
provided by Zelinski (2009). Additionally, Lustig et al. (2009) provide a detailed
consideration of the possibility of using neuroimaging data “as a guide to identify core
cognitive processes that can be trained in one task with effective transfer to other
tasks that share the same underlying processes” (Lustig et al., 2009, p. 504).
in two pioneering studies by Jennings and Jacoby (2003) and Jennings and colleagues
(2005) focused on helping older individuals, at the time of recalling information, to
improve their ability to recollect information. The training sessions involved a highly
challenging task that aimed to improve recollection in two ways. First, the training
sessions began at a level at which older adults could accurately perform the task, but
then the difficulty level was systematically increased, on a case-by-case basis, as the
participant mastered each level. Second, for each item that the participant answered,
he or she was provided immediate feedback as to whether the response was correct.
If the participant’s response was correct, the computer “beeped” and the message
“correct” appeared on the screen. If the participant’s response was incorrect,
no message appeared. This directly and prominently signaled to older adults when
they were correct, and when they had made errors.
For reasons that will soon become apparent, the task the older adults were asked
to perform has come to be called the “repetition-lag” paradigm. First, participants are
presented with a list of 30 words on the computer screen and are asked to read each
word aloud and remember it. Then, they are given a “yes/no” recognition test, consist-
ing of the 30 words they have just studied, plus 30 new words. However, the new
words are not just presented once. Each new word is presented twice during the recog-
nition test phase (thus the “repetition” portion of the name for this procedure). For
one-half of the repeated new words, the first and second presentation of the new word
occur quite closely to one another in time; for the remaining half, the first and second
presentation of the new word is spaced apart—with a long rather than short “lag”
between the first appearance and its second appearance (thus the “lag” portion of the
procedure’s name). Crucially, participants are instructed to say “yes” only to the words
that they have earlier read aloud, during the study phase, and to be sure to say “no” to
all of the new words, both if they are being shown the new word for the first time, and
if the new word had been shown earlier but during the recognition test, rather than
during the reading task.
Earlier research (Jennings & Jacoby, 1997) showed that, compared with younger
adults, older adults often made many errors on this task, mistakenly saying “yes” to
the new words that repeated during the test phase, particularly if there was a longer
lag between the first and second presentation of the word. Such errors would arise if
individuals made their recognition decisions only on the basis of whether the word
seemed to be familiar and did not try to determine the precise source (e.g., M. K.
Johnson, Hashtroudi, & Lindsay, 1993; K. J. Mitchell & Johnson, 2009) of that famil-
iarity: that is, was the word one that they had read aloud earlier or one that had
occurred at an earlier time during the testing?
The objective of the training procedure used by Jennings and Jacoby (2003) was to
encourage older adults to pay closer attention to the evidential grounds for their
recognition decisions and to try to recollect the source of the information rather than
responding only on the basis of familiarity. To do this, these researchers gave older
adults not one, but many study-test cycles of the repetition-lag procedure, across sev-
eral days of training (four sessions a day, for a total of 7 days, with all the training days
immediately consecutive to one another except for the intervening weekend). In the
initial sessions, they used only a very short lag, with only one intervening item
between the presentation of the new item, and its re-presentation, plus one slightly
Making Br ain Paths to Agil e T h in k in g , Part 2 553
longer lag (two items), that posed a greater challenge and to which older adults often
incorrectly responded “yes.” As performance improved at a given lag (up to the accu-
racy level previously shown by young adults at that lag), the researchers increased the
lag between items, gradually incrementing the shorter and longer lag from 1 and 2; to
1 and 3; then 2 and 4; 2 and 8; 4 and 12; 4 and 16; 8 and 20; 8 and 24; 12 and 28; 12
and 32; 16 and 36; 16 and 40; 20 and 44; and finally, 20 and 48. The lags were chosen
such that individuals were always working at one lag that they had mastered and
another lag that was still challenging, and participants continued with a given interval
pair until they had achieved criterion (defined as the average accuracy level of younger
adults at the same interval).
Individuals in the training group improved markedly compared with a group that
was exposed to a similar series of study-test cycles, but without the performance-
guided systematic increments of the lag intervals (the control group received a “yoked”
set of lag intervals, but in a randomly intermixed manner). Although the controls also
noticeably improved (mean lag mastered by the end of training = 10.2 items, compared
with 1.83 at the outset), the benefit in the experimental group more than doubled that
of the control group (27.92 at the end, compared with 1.92 at the outset). These results
concur with, and extend, other test-specific training interventions with older adults,
demonstrating that “older individuals retain a reserve capacity or cognitive plasticity
that can be utilized to improve memory function” (Jennings & Jacoby, 2003, p. 436)
not only in tasks that focus on encoding but also in tasks that focus on retrieval.
Equally important, a further study, using a largely similar training procedure, dem-
onstrated that the benefits derived from “training in recollection” (and attentiveness
to the use of familiarity vs. recollection) had “carryover” benefits to other types of
tasks. Jennings et al. (2005) found that, compared with a recognition practice control
group, recollection training not only improved performance on the trained procedure
but also led to significant improvements on several other transfer tasks. Pre- to post-
training improvements were found on four other tasks: a working memory task (an
n-back task, in which participants were asked to study each letter and indicate whether
it was the same as a letter presented “n” trials earlier, e.g., 1, 2, or 3 trials before), a
task involving self-ordered pointing (in which participants were required to point once
only to each of 16 different abstract shapes presented on 16 different pages), a differ-
ent memory task requiring discrimination between words that had been presented in
auditory form versus words that the participants had themselves read, and a digit
symbol substitution task (from the WAIS-R), in which participants were asked to sub-
stitute nine different symbols corresponding to designated numbers for a list of num-
bers. Thus, the recollection training procedure produced benefits that extended
considerably beyond the particular training procedure, “encompassing working
memory with letter stimuli, output monitoring with abstract shapes, and source dis-
crimination for presentation modality [. . . showing benefits] to near transfer mea-
sures regardless of stimuli type and for both working and long-term memory demands
[. . . and] suggesting that targeting recollection for training does not improve a memory
system per se but may enhance processes that are applicable across multiple systems”
(Jennings et al., 2005, p. 295).
This observation of considerable across-task benefits of the training contrasts with
many previous training studies, in which benefits of training are observed only for
554 BRAIN AND ENVIRONMENT
tasks and skills similar to those on which participants have trained (e.g., Kramer &
Willis, 2002). Notably successful and adept performance on the various tasks that
showed transfer gains in Jennings et al. (2005) draws on several cognitive, perceptual,
and/or attentional processes, beyond item-specific recollection, that are important to
flexible thinking, such as the updating of working memory (n-back), output monitor-
ing (self-ordered pointing), and sustained attention (symbol substitution) 11. This study
of Jennings et al. (2005) involving training in episodic recollection with older adults—
like the later study focusing on training in working memory in younger adults reported
by Jaeggi et al. (2008; discussed in the section on “Recently Acquired ‘Experimentally
Assigned’ Expertise and Brain Plasticity in Humans”) that showed benefits from work-
ing memory training on a measure of fluid on-the-spot reasoning—points to consider-
able transfer benefits from training in memory (and concurrent attention) for mental
agility. In the next section we will further consider transfer benefits from tasks that
focus on training our ability to adeptly exercise where and to what we attend.
T R A I N I N G AT T E N T I O N A L C O N T R O L : D UA L - TA S K VA R I A B L E -
PRIORITY TRAINING, AND REAL-TIME VIDEO GAMING
Beneficial effects of cognitive-behavioral training in older, and also younger, individu-
als may be increased—and also show greater generalization to other tasks—if the
training procedure that is used is deliberately made to vary, placing strong demands
on the individual’s ability for flexible and dynamically changing responding (Bherer
et al., 2005; Kramer et al., 1995. Also see Chapter 5 and R. A. Schmidt & Bjork, 1992,
regarding the benefits of “learning to vary,” and Gopher, Weil, & Siegel, 1989, for a
broad conceptual overview, based on models of skills and theories of attention, for
how “emphasis change” may foster development of beneficial strategies in highly com-
plex problem-solving domains.)
One such procedure involves what has been called “variable priority training.” Such
training requires the individual to rapidly switch priorities among two or more tasks
that are performed concurrently. Rather than being instructed to place equal empha-
sis on each of two tasks to be performed together (fixed priority training), in variable
priority training participants might be asked to allocate changing amounts of effort
and attention to one or the other task, in proportions of, for example, 20–80, 35–65,
50–50, 65–35, and 80–20. The designated proportions would require the participant
to comparatively emphasize his or her speed and accuracy of performance on one task
(say alphabet arithmetic, in which individuals must subtract or add letters, as in “K–3
=?” for which the answer is “H”) compared to another task (e.g., a continuous gauge
monitoring task). In an important early study by Kramer and colleagues (1995), across
eight experimental sessions (including an initial screening session) both younger and
older adults received training on each of the tasks separately, as well as together, with
individuals assigned to either variable priority or fixed priority training. Feedback
reflecting a combination of both speed and accuracy of performance was given both
continuously for the last five trials and for each 5-minute block of trials. Participants
were also tested on two transfer tasks (a scheduling task, and a paired-associates
running memory task) for which feedback was given only at the end of each 5-minute
block, rather than continuously.
Making Br ain Paths to Agil e T h in k in g , Part 2 555
As expected, and consistent with many previous studies, at the outset of training,
the older participants were generally both slower and less accurate than were the
younger participants, and also showed a larger performance decrement as a result of
the dual task compared to single task requirements. Both older and younger adults
were able to vary their performance as requested by the variable priority instructions.
Most relevant here were the training effects. The results showed that, for both older
and younger adults, training yielded improvements in both response times and accu-
racy for both the monitoring and alphabet-arithmetic tasks. These effects were larger
for the variable priority than for the fixed priority training—even though the test
conditions involved 50–50 emphasis for everyone, and the variable priority group had
far less training on this particular emphasis condition than did the fixed priority
group. In addition, transfer was greater for those in the variable priority than in the
fixed priority condition particularly under the dual-task requirements.
Crucially, from the perspective of the iCASA framework, it appeared that variable
priority training led to both increasing automatization of single task components of
the dual tasks and a more general increase in the ability to effectively coordinate or
manage multiple tasks. On the one hand, increasing automatization in the variable
priority condition was particularly clear on the alphabet arithmetic problems, as
shown by an overall improvement in the speed of performance and in significantly
larger decreases in the slope of the function for adding versus subtracting letters
(“addend-subtrahend slope;” cf. G. D. Logan, 1988, 2002) with increasing training.
Decreases in the addend-subtrahend slope were significantly larger for the variable-
than for the fixed-priority training condition for both older and younger adults.
On the other hand, a more general increase in the ability to coordinate or manage
multiple tasks was shown in significantly greater response time improvements on the
new transfer scheduling task, and also in significantly greater response time and accu-
racy improvements in the new transfer paired-associates task, particularly under
dual-task conditions, for the variable priority than for the fixed priority condition.
These variable-priority transfer-training benefits were found for both older and
younger adults, suggesting that the three training sessions on the original tasks
enabled both age groups to learn a dual-task processing skill that generalized to new
contexts and tasks. Paralleling many previous studies that have shown that more
difficult initial learning conditions may yield stronger longer-term learning and trans-
fer (R. A. Schmidt & Bjork, 1992), these greater transfer benefits for the variable-
compared with the fixed-priority conditions were accompanied by relatively poorer
performance in the early training sessions, particularly for older adults. This suggests
that variable-strategy training needs to persist beyond an initial phase of increased
costs or difficulty.
A further study, using broadly similar methods and feedback, but with simpler
auditory and visual discrimination tasks for the primary training component, again
showed that training enhanced performance on both the trained tasks and transfer
tasks for both older and younger adults (Bherer et al., 2005; see also Bherer et al.,
2006). The transfer benefits for older individuals were at least as large as those for
younger persons—and larger in the case of an accuracy measure. Testing of a subset of
the participants 1 month later additionally suggested that the benefits were main-
tained across this intervening delay. More recent work has also shown that both age
556 BRAIN AND ENVIRONMENT
In other work, Basak and colleagues (2008) examined the effects of training in
another commercial real-time strategy video game—called Rise of Nations—on the
executive and cognitive function of older adults. The game requires participants to
build new cities, improve city infrastructure, and expand one’s national border through
a wide range of strategies, such as diplomacy, technology races, building “wonders,”
and espionage. The participant can explore broader or more detailed parts of the entire
map and must continually monitor his or her resources and situation, as well as plan
methods for protecting and expanding his or her territories.
Thus, like the Medal of Honor game used by Green and Bavelier (2003, 2006), the
strategy-based Rise of Nations game appears to place high demands on multiple
aspects of executive control, such as switching between various goals and priorities,
and maintaining multiple sources of information in working memory. However, unlike
the Medal of Honor game, the Rise of Nations is not a first-person shooter game, and
therefore it does not place the same demands as does the former on visual-spatial
attentional abilities, such as selective and focused attention. These similarities and
differences led Basak and colleagues (2008) to predict that whereas extensive playing
of the Rise of Nations game would yield broad transfer gains on measures of executive
control and memory, there would be fewer transfer gains on speeded visual-perceptual
processing tasks. Forty older adults who were naïve to video games were randomly
assigned to either 7–8 weeks of video game playing (total training time of 23.5 hours)
or to a no-contact control group. Both groups were tested on a cognitive battery pre-
and posttraining, and final data were collected from 19 participants in the training
group, and 20 participants in the control group.
Whereas the video training had no effect on one measure of working memory
(operation span), training yielded a significant reduction in switching costs associated
with a task-switching procedure and also focus or object-switching on an N-back task.
Training also improved detection in a visual short-term memory task particularly
when the number of stimuli was near the capacity limit (four items). Notably, signifi-
cant training related benefits, especially after 23.5 hours of training, additionally were
found on a measure of on-the-spot fluid reasoning (Raven’s Advanced Progressive
Matrices). Individual differences in improvements in game playing were correlated
with improvements on the N-back and task-switching measures (but not the reason-
ing or visual short-term memory measures). As predicted, measures of visual-spatial
performance (functional field of view, attentional blink, enumeration) were not
affected by the training on the Rise of Nations game.
On the one hand, inasmuch as the video game involved such tasks as “maintaining
items in short-term memory, juggling things back and forth in a short span of time,
and making decisions on various strategies and resources” (Basak et al., 2008, p. 776),
it might be suggested that the transfer effects observed, on tasks measuring visual
short-term memory, switching between objects, and reasoning abilities, comprised
“near transfer” benefits. On the other hand, the many differences between the video
game context and the standardized measures of executive function and reasoning on
which transfer benefits were demonstrated might be construed as involving a form of
distant transfer.
Although it is difficult to definitively isolate the factors responsible for the
action-video induced improvements in younger and older adults, particularly in
558 BRAIN AND ENVIRONMENT
contrast with many of the programs that have been designed for the specific purpose
of “brain training,” such games are remarkable for their complexity, and the manner in
which they simultaneously and in parallel place demands on multiple brain systems:
In video games developed for entertainment, for instance, one may be simul-
taneously engaged in memory tasks (e.g., spatial memory for the route to the
enemy fortress, semantic memory for weapons at one’s disposal or enemies
still active), executive tasks (e.g., resource and weapon allocation, dual task-
ing), visual attention tasks (multiple object tracking, distractor rejection),
visuomotor tasks (e.g., steering, piloting), and rapid object recognition, to
cite just a few. (C. S. Green & Bavelier, 2008, p. 696)
Similarly, Basak and colleagues emphasize the variability and the dynamic changes
in flexibly adaptive responding called upon by the Rise of Nations game:
Like the variable priority training work of Kramer et al. (1995), certain video games
appear to require varied, flexible, and integrative responding to dynamically changing
contexts. Notably, as also remarked by C. S. Green and Bavelier (2008), requirements
for such parallel, multiple and simultaneous, modes of processing are also characteris-
tic of some natural learning and performance activities that may also yield benefits to
cognitive flexibility, such as music and sports or athletics training. Beyond calling
upon both automatic and controlled processes, such parallel modes of processing par-
ticularly may call upon relatively higher levels of hierarchical organization and infor-
mation processing that help to promote generalization of learning to new tasks and
contexts (cf. Ahissar & Hochstein, 2004). Thus, both action video games such as Medal
of Honor and complex strategy games such as Rise of Nations, which draw on multi-
ple, simultaneous, and varied modes of processing, may help to extend an individual’s
oscillatory range in levels of control and/or levels of specificity, and they may promote
mental agility in contexts that extend beyond the game-playing scenario.12
Nonetheless, it is also important to be a “healthy skeptic” with regard to such
possibilities and to take into account the vast diversity of video games, each one of
which may call upon somewhat different skills and abilities or dynamic combinations
and recombinations of skills, and may thus have somewhat differing implications for
the nearer and farther transfer of those abilities. Additionally, it is important to rec-
ognize that the potential benefits of engagement in this activity, as for virtually all
activities do not occur in isolation from competing alternatives for behavioral engage-
ment. There are, here, as so often, trade-offs and “opportunity costs”—time spent
video-gaming is time not spent on some other potential activity that might bring
different benefits—and excessive devotion to any one activity may bring costs to
Making Br ain Paths to Agil e T h in k in g , Part 2 559
individuals of all ages, including young children, if engagement in other pursuits, such
as reading, writing, or academic preparation is forfeited (e.g., Weis & Cerankosky,
2010; see also Bailey et al., 2010).
AT T E N T I O N R E S TO R AT I O N T H E O R Y A N D E X P E R I E N C E S
O F T H E N AT U R A L E N V I R O N M E N T
The central concept in attention restoration theory is that of “directed attention” or
what was earlier, following William James (1890/1981), termed “voluntary atten-
tion.” Largely under intentional control, directed attention involves the capacity to
inhibit or block competing stimuli or distractions during purposeful activity and so
assumes a crucial role in such diverse aspects of behavior as novel problem solving,
resisting distractions, inhibiting undesired impulses and inclinations, and focusing on
weak or ambiguous stimuli. It also enables efficient and effective selectivity of
processing in both thought and perception, so that we can more readily separate the
essential and important from the inessential and less important.
As observed by S. Kaplan (1995, p. 171), voluntary directed attention is “not, in
itself, more important to problem-solving than knowledge or perception or action”
nor is it “necessarily the most important component of the system necessary to gener-
ate appropriate behavior.” However, it is fragile—and particularly is vulnerable to
fatigue—and therefore often comprises a weak link in our informational processing
nexus. Similar to self-regulatory resource depletion theory, discussed in Chapter 5
(see also S. Kaplan & Berman, 2010), attention restoration theory emphasizes the
effortful nature of focused attention and “views directed attention as a global
inhibitory mechanism such that fatigue from one task transfers to other tasks that
subsequently require directed attention” (S. Kaplan, 2001, p. 482).
Four broad suggested approaches to restoring directed attention have been out-
lined by S. Kaplan (1995, 2001). One is closely reminiscent of that suggested by
Elsbach and Hargadon (2006, alluded to in Chapter 5, and further discussed in Chapter
12) regarding the need for structuring “recharge times” in organizational workdays.
This approach is simply to avoid situations that might draw on the need for directed
attention, particularly situations where there is insufficient or inappropriate informa-
tion, where one has “inappropriate” motivation, inadequate skill, or situations that
require consideration of multiple competing mental models (S. Kaplan, 2001).
Avoiding such highly taxing situations, and instead immersing oneself in contexts
characterized by heightened compatibility with one’s own inclinations and aims, may
help to restore attention; the compatibility may be motivational and/or informational.
Other approaches involve experiencing “a sense of being away,” via settings or con-
texts that provide either physical or mental relief from daily concerns, and becoming
immersed in a coherently ordered environment of substantial scope or “extent,” again
either physically, as in encountering expansive horizons, or conceptually, as when the
presence of historical artifacts promotes a sense of connectedness to a much larger
and more extended past.
Perhaps most researched, however—and also most directly related to the iCASA
framework’s emphasis on the need for “oscillatory range” in levels of control—is the
restorative capabilities of a form of “involuntary” or spontaneous attention to
560 BRAIN AND ENVIRONMENT
presentation rate, response times were also significantly faster. In contrast, viewing
geometrical patterns did not lead to attention benefits.
Adopting an especially sensitive within-participant design, Berman et al. (2009)
demonstrated that compared with viewing photographs of urban cityscape scenes,
viewing photographs of natural scenery (from Nova Scotia) led to improvements on
two different measures of directed attention. University student participants were
first administered the Attention Network Task, a task designed to differentiate
between three behaviorally and neuroanatomically separable aspects of attention,
including alerting, orienting, and executive attention. Attentional alerting was
assessed by contrasting trials in which a central cue warned participants than an
upcoming trial was about to appear, versus trials in which no cue is given; typically,
participants’ performance is facilitated by the alerting cue. Attentional orienting
similarly was assessed by contrasting two types of trials but here the cue additionally
provides participants with guidance as to the location of the upcoming trial informa-
tion, with cues at either the top or bottom half of the screen contrasted with a cen-
trally displayed cue. Third, executive attention was assessed by trials in which a
centrally displayed arrow either pointed in a direction congruent with that pointed to
by four additional surrounding (flanking) arrows or pointed in an incongruent direc-
tion; these trials require the greatest amount of directed attention. After the Attention
Network Task, participants were shown either approximately 10 minutes of natural
scenery photographs (50 photographs, with approximately 7 seconds per picture) or
10 minutes of photographs of the built environment, after which they were again
given the Attention Network Task. The order of the intervening photographs was
counterbalanced across participants, with 1 week separating the two experimental
sessions (either nature, then urban views, or vice versa).
Berman and colleagues (2009) found that compared with viewing the urban
scenes, viewing the natural scenes lead to significantly enhanced performance on the
executive attention trials of the Attention Network Task. (Note that this result,
involving selective performance enhancement on the executive attention trials, thus
directly parallels that found using integrative body-mind training, reported by Tang
and colleagues, 2007, 2009, and discussed in the first section of Chapter 3.) These
benefits were not related to changes in mood, although, as expected, participants
rated the viewing of the pictures of nature as significantly more refreshing and more
enjoyable than the viewing of the urban areas, and they also liked the nature pictures
significantly more. In addition, and replicating an earlier experiment that instead
involved actually walking in an urban setting versus a natural setting (Berman et al.,
2009, Experiment 1), exposure to nature also led to significantly improved backwards
digit span.
At the most immediate level, these results, and those of the other studies reviewed
in this section, show that “simple and brief interactions with nature can produce
marked increases in cognitive control” (Berman et al., 2009, p. 1211). At a broader
level, these outcomes have implications that may reach far beyond that of the cogni-
tive scientist’s laboratory, suggesting that “to consider the availability of nature as
merely an amenity fails to recognize the vital importance of nature in effective cogni-
tive functioning.” Immersion in interactions with nature provides one important
means whereby restoration of our capacity for directed attention may emerge.
562 BRAIN AND ENVIRONMENT
In very general terms, European, North American, and Japanese adult groups
tend to respond to scenes as natural if the landscape is predominantly
vegetation, water, and mountains, if artificial features such as buildings,
automobiles, and advertising signs are absent or inconspicuous, and if the
dominant visual contours or edges are curvilinear or irregular rather than
starkly rectilinear or regular. (Ulrich, 1993, p. 95)
Research also needs to evaluate the ways in which all of the key characteristics
identified by attention restoration theory, including not only fascination but also
compatibility, a feeling of extent, and a feeling of “being away,” can be realized in the
design of our built environments and the ways in which we can draw on those charac-
teristics to creatively modify our environments, with aesthetic and natural objects of
all sorts, to best promote human flourishing.
T R A I N I N G O F AT T E N T I O N — I N Y O U N G C H I L D R E N —
ALSO IMPROVES FLEXIBLE THINKING
The effects of particular forms of environmental stimulation on flexibly adaptive
thinking also may be examined for individuals at the other end of the developmental
spectrum. A prominent and changing aspect of the young child’s cognitive capacity
involves attention. Children between the ages of 3 and 7 years typically show pro-
nounced improvements in their ability to voluntarily control attention. Although
much of this development may be related to maturational processes, researchers have
recently begun to examine whether environmental factors, particularly exposure to
Making Br ain Paths to Agil e T h in k in g , Part 2 563
activities that challenge the child’s current level of voluntary attention control, may
help to accelerate this developmental process.
Rueda, Rothbart, McCandliss, Saccomanno, and Posner (2005) devised several
procedures that young children, between the ages of 4 and 6 years, found engaging
and that systematically posed increasing challenges to the child’s executive attention
capacity. In a pretraining phase, children in the experimental groups first learned to
track a cartoon cat on a computer screen by using a joystick. They initially helped the
cat to stay on grassy (nonmuddy) areas of the screen, then helped the cat to stay dry
by tracking it with an umbrella, and then assisted it to find food in a maze. Five days
of training exercises then began, divided into 9 or 10 sessions, with each exercise
becoming more difficult as the child reached a given level of performance (e.g., correct
on three consecutive trials).
The sessions focused on three aspects of attention: anticipation (using the joystick
to anticipate where a duck would emerge from a pond, at first when it remained visible
throughout, then when it was submerged for part of its trajectory), stimulus discrimi-
nation (remembering different multiattribute cartoon characters to be selected from
an array of characters), and conflict resolution (choosing the larger of two arrays,
when the arrays themselves consisted of numbers, that either agreed or disagreed
with the size of the array). Six-year-old children also completed an inhibitory control
(go/no-go) exercise that required them to click the mouse button as quickly as possible
to sheep that appeared, but not to click in response to wolves that appeared in sheep’s
clothing. Children in the experimental attention-training condition were compared
with age-matched control groups who came to the laboratory just for pre- and post-
training assessments of attention and intelligence (Experiment 1) or also for several
intervening control laboratory sessions in which they watched popular children’s
videos (Experiments 2 and 3).
Results showed that the 4-year-olds given the attention-training sessions signifi-
cantly improved on two measures of intelligence: the abstract fluid-reasoning portion
(Matrices) of the measure of intelligence (the Kaufman Brief Intelligence Test) and
also on the total score of the intelligence measure (Matrices plus Vocabulary). This
improvement was not found for their comparison group: There was a significant
group by pre/post-assessment interaction for both measures. Notably, as we have seen
(e.g., in Chapter 9) the Matrices task is a well-accepted measure of fluid on-the-spot
thinking, nonverbal reasoning, and simultaneous processing—all aspects directly
related to agile thinking.15 In contrast, in the 6-year-olds, behavioral improvements in
performance on these measures were less pronounced. However, the researchers
also obtained electrophysiological measures (EEGs) during the performance of the
attention test that was given in the pre- and postassessment sessions (the Child
Attention Network Test), and the event-related potentials (ERPs) from this task
showed different patterns for the trained versus nontrained older children.
The Child Attention Network Test measures the ability to resolve conflict in
responding to different stimuli. In this task, a central fish is presented, with four
“flanking” fish, which either point in the same direction as the central fish, corre-
sponding to the direction the child is required to indicate (congruent trials), or point
in the opposite direction (incongruent trials). A comparison of the ERPs for the con-
gruent versus incongruent trials showed that the older children—very much like
564 BRAIN AND ENVIRONMENT
activities with another child that help to model and support processes of self-monitor-
ing. During this activity, again done in pairs:
One child has a “hand” and counts out objects while the other child checks
whether the counting has been correct (the second child serving as a regula-
tor of the first child’s performance). The child who is the “checker” waits until
the first child finishes counting out the number of objects and then, using a
checking sheet, makes sure the answers are correct. This supports self-reflec-
tion as well as inhibition. The child who checks inhibits the desire to act until
it is his or her turn. The “counter” engages in self-reflection while watching
the checking, reflecting on his/her previous answer, thinking about whether
it’s correct or not […]. “Reliving” one’s actions by watching someone check is
practice in self-reflection on action, a metacognitive aspect of [executive
functions]. (A. Diamond et al., 2007, supplemental online material, p. 5)
Other joint activities, such as that of planning play scenarios, encourage children
to think before acting. They also draw on working memory and inhibitory capacities as
the children remember the scenario they had planned and inhibit impulsive behaviors
inconsistent with their agreed-upon roles.
A. Diamond and colleagues (2007) were given the opportunity to evaluate the
effects of the Tools of the Mind program versus another new high-quality curriculum
on standardized measures of executive function when a low-income urban school dis-
trict in the Northeast opened a new publicly funded preschool program. Importantly,
the school district agreed to randomly assign teachers and children to these two, newly
instigated, curricula. The two programs had equivalent resources such as books, toys,
and furniture, and equivalent state-set standards, such as a student-teacher ratio of
not more than or equal to 15:2. Stratified random assignment was used to allocate
teachers and assistants to the two programs. The comparison curriculum was a “bal-
anced literacy” curriculum, designed to teach children literacy skills through a bal-
anced combination of reading, writing, and listening activities, in the context of
particular themes, such as “family” or “transportation.” It was a typical and high-qual-
ity curriculum that had the same academic content as the Tools program but differed
in the broad educational focus, and there were no activities explicitly and intentionally
designed to promote executive function.
The two programs were run over a period of 2 years. In the first year teachers for
both curricula were given a 4-day training workshop; additional training days were
also given in both the first and second years. Children in the two groups were closely
matched on age (mean of about 5 years), ethnicity (approximately 90% Hispanic),
income (approximately 78% with family incomes of less than $25,000/year), and
mother’s education. Data were reported for 62 children in the comparison curriculum
and 85 children in the Tools curriculum; the parents for 91% of the Tools, and 76% of
the comparison group, gave consent for their children to be tested on the executive
function measures.
Two tasks were used to assess executive function: a “dots task” and a “flanker task.”
The dots task was a spatial compatibility or Simon effect task, in which a red heart or
flower appeared on the right or left of the computer screen, and was given in three
566 BRAIN AND ENVIRONMENT
In the next and final section, we consider whether a similar approach, involving the
encouragement of increased “playful practice” and the pursuit of novel and engaging
activities, might likewise yield benefits for the novel problem-solving and on-line
reasoning capabilities of older individuals.
N O V E L A C T I V I T I E S , P L AY F U L P R A C T I C E ,
AND IMPROVING AGILE THINKING
Several lines of evidence, reviewed in earlier sections of this chapter, converge in
pointing to the possibility that older adults may, under appropriate conditions, show
much more flexible and adaptive thinking than might otherwise be expected on a
“standard view” of the cognitive declines associated with normal aging. These studies
suggest that environmental conditions that invite the use of agile thinking may be
surprisingly important in maintaining cognitive performance. They further suggest
568 BRAIN AND ENVIRONMENT
Looking Back
We have now completed the paired chapters on “making brain paths to agile thinking”
and, with this, also the third part of the book, broadly focused on the brain, the envi-
ronment, and their manifold interactions. In these last two chapters we have turned
to consider the numerous ways in which the environments in which we live, work, and
play continuously and dynamically shape the structure and functional organization
and connectivity of our brains—and also render us either more or less likely to sustain
570 BRAIN AND ENVIRONMENT
agility of mind both in immediate or shorter term contexts, and across years and
even decades.
At the outset, we first considered the broad notion of brain plasticity, as well as
evidence that both sensory-motor and more complex forms of learning lead to associ-
ated changes that also can be demonstrated to have specific functional behavioral rel-
evance. After an introduction and several illustrative examples of the concepts of
brain reserve, cognitive reserve, and “compensation,” we then considered the exten-
sive, but still in some cases surprisingly inconclusive and mixed findings from longitu-
dinal and epidemiological investigations of the role of such factors as years of formal
education, the nature of one’s occupation, one’s social interactions, and one’s leisure
pursuits in contributing to later-life cognitive performance and to the likelihood and
probable age of onset of dementia. We found that there was considerable support for
the role of social and occupational factors (and also the regular use of a second lan-
guage) in promoting longer term adaptive cognitive function, and for the benefits of
engaging in cognitively stimulating leisure activities in reducing dementia risk and/or
age of onset. Benefits of physical exercise and cardiovascular fitness were demon-
strated in a number of longitudinal studies, with regular exercise associated with
reduced cognitive decline and also improved performance on such outcome measures
as working memory, visual-spatial performance, and conceptualization.
Turning, for one section, to focus primarily (although not exclusively) on the other
end of the developmental spectrum, we noted the adverse consequences of many
forms of physical and psychosocial stressors that are associated with poverty and
deprivation in children. We considered evidence that some functional neurocognitive
systems, such as those involving language, memory, and cognitive control may be
particularly vulnerable to disruption by stress. Possible pathways to such detrimental
effects, such as increased allostatic load, changes in the automatic processing of
novelty in prefrontal cortex, and the adverse effects of particularly prolonged and
intense stress on glucocorticoid receptors in the hippocampus, leading to possible
alterations in hippocampal function, were noted.
Returning to interventions with older individuals, two “field experiments,” includ-
ing the Experience Corps program in Baltimore and the Senior Odyssey program, were
found to lead to such benefits as increased physical strength and greater perceived
social support, as well as modest improvements on some standardized neuropsy-
chological outcome measures (e.g., inhibitory processing and inductive reasoning).
These field experiments bridged to interventions that specifically use fully random-
ized assignment to experimental and comparison groups and that provide the most
persuasive evidence for the benefits of a given factor in fostering mental agility.
We saw that investigations of “environmental enrichment” with a wide range of
animals, though primarily rats and mice, and involving the opportunity for both
novel and varied exploration and learning, yielded strong evidence for enhanced
performance on multiple behavioral indices that could be construed as measures of
adaptive flexibility. Animals from enriched environments (e.g., involving tunnels,
balls, ladders, and other toys, as well as “social” opportunities), demonstrated improved
reversal and discrimination learning, more rapid “unlearning” of no longer appropri-
ate behaviors, and greater success in finding hidden food in a novel environment, than
did animals from nonenriched environments. Equally important, we saw that these
Making Br ain Paths to Agil e T h in k in g , Part 2 571
In this final chapter, we will consider implications and applications of the iCASA
framework, and we will outline some of the many important research questions that
remain regarding when, and how, we can more consistently and more optimally realize
the forms of adaptive flexibility in thought and action that our agile minds can make
possible.
The chapter is organized in the form of broad questions that are then expanded by
selected reminders of key findings, additional evidence regarding possible applications
or implications, and more specific questions and research directions. My primary aim
in this concluding chapter is to “put the iCASA framework to work” and to identify the
sometimes surprising implications and possibilities opened up by this way of looking
at our minds. A secondary aim, accomplished through the question-plus-elaboration
format, is both to underscore some of the central findings we have considered and to
interrelate and integrate findings across and within chapters. To this end, the ques-
tions span all three parts of the book—memory, categorization, and concepts; motiva-
tion and emotion; and brain and environment. Additionally, although many of the
outstanding research questions will involve experimental efforts with individual
participants, others will involve larger scale empirical investigations, of formal and
informal groups and organizations. The questions are very broadly grouped into four
sections, concerning (a) oscillatory range in levels of specificity and levels of control;
(b) environmental enrichment and stimulation; (c) the interpenetration of concepts
with perception, action/motivation, and emotion; and (d) broader educational, policy,
and ethical implications.
573
574 BRAIN AND ENVIRONMENT
that shifts in the processing mode we adopt are unlikely to occur automatically.
Rather, as succinctly summarized by A. C. Olsson et al. (2006, p. 1381) “there may be
nontrivial constraints on people’s ability to shift to the process that is appropriate to
the task.”
Interventions to aptly modify the predominant LoS and/or LoC that individuals
adopt during a given task could be more precisely targeted and calibrated so as to
optimize performance if frequent or even continuous measures of an individual’s
LoS and/or LoC could be obtained. These measures might be comparatively indirect,
taking the form of talk-aloud protocols, similar to those that allowed relatively con-
tinuous tracking of LoS during the computer programming design problem-solving
tasks examined by Guindon (1990), and that are graphically portrayed in Figures 7.2
and 7.3. Alternatively, the measures might be more direct, in the form of a continuous
“radio-dial-like” report during an ongoing task, or of discrete self-reports of the level
of control that had been required for particular items or portions of a task, similar to
those that have recently been reported by Morsella et al. (2009) during the perfor-
mance of control-demanding tasks such as the flanker and Stroop color word interfer-
ence tasks. Morsella and colleagues (2009) found that participants’ self-reports of
perceptions of control, as well as of difficulty and competition, systematically varied
with experimental conditions that manipulated the level of response interference that
was present on individual trials. As proposed by these investigators, just as response
times “can reveal aspects of cognitive processing that may not be detectable through
less subtle behavioral measures (e.g., response accuracy), measures of the subjective
aspects of processing may illuminate features of cognitive processing that are unde-
tectable in standard behavioral and psychophysiological measures” (Morsella et al.,
2009, p. 1822).
Recent approaches such as that of Badre and colleagues (2010) to evaluate the
neural correlates underlying self-initiated discovery of rules at different levels of
abstraction (discussed in Chapter 8, in the section on “Neuroimaging Evidence for
Hierarchical and Functional Distinctions within Frontal and Prefrontal Cortex”) may
also provide guidance as to the conditions that can bolster versus impede adoption of
a strategy that is well matched to the particular stimuli and task demands currently in
hand. Based on their behavioral findings that, using trial-by-trial feedback, partici-
pants successfully acquired both a concrete and a higher order rule, combined with
their neuroimaging results pointing to corresponding changes in patterns of activa-
tion along the anterior to posterior axis, these investigators argue that the anterior-
to-posterior architecture of the frontal cortex “may support rapid learning of action
rules at multiple levels of abstraction.”
The extent to which such “parallel search” at multiple levels of abstraction might
predominantly involve deliberate, top-down controlled search, versus also momen-
tary or interspersed phases of less deliberate, perhaps intuitive, familiarity-based or
automatic processes, remains unclear, though additional interregional connectivity
analyses performed by Badre et al. (2010) suggested complex dynamic interactions in
which the frontal cortex both influences, and is influenced by, the striatum.
Two additional implicit procedural interventions that may encourage changes
(or greater oscillatory range) in LoS and LoC are engaging in a simple cognitive-
perceptual task requiring the generation of alternative uses of common objects
(the Alternative Uses Task), and thinking about one’s core values, goals, and ideals
(self-affirmation). We saw (in the third section of Chapter 2) that performing alterna-
tive uses categorization for a brief period of time (10–15 minutes) before attempting
to solve problems reliably improved performance on ill-defined tasks that are typically
solved through insight (Chrysikou, 2006) and also significantly enhanced perfor-
mance on tasks requiring novel, on-the-spot visual-spatial analogical and fluid reason-
ing (Wen, Butler, & Koutstaal, in preparation). A brief period of self-affirmation,
requiring participants to think and write about personally important values, similarly
bolstered both subsequent insight and visuospatial fluid reasoning performance
(Chapter 6, “Self-Affirmation and Flexible Thinking”).
This then raises the question of how combining these interventions might affect
thinking and problem solving: What aspects of the alternative uses categorization
task, specifically, are responsible for the observed beneficial transfer effects to insight
and fluid reasoning problem solving? If self-affirmation and alternative uses categori-
zation lead to changes in cognitive flexibility, and cognitive flexibility is itself an aspect
of executive function, can the intervention effects be isolated to one or more subcom-
ponents of executive function that have been identified by other researchers (e.g.,
Miyake et al., 2000), such as shifting, or updating?
As noted, there is evidence to suggest that one of the immediate effects of self-
affirmation interventions is to increase the level of abstraction at which individuals
identify common actions (Chapter 6; Schmeichel & Vohs, 2009; Wakslak & Trope,
2009). This, then, also raises the question as to whether this intervention—similar to
what has been found in relation to changes in construal level as a function of changes
in an individual’s temporal orientation (Chapter 3; especially Förster, Friedman, &
Liberman, 2004)—may also sometimes be detrimental, on the one hand fostering
improved performance on tasks that require greater abstraction (or, at least, a higher
level of abstraction than individuals tend to spontaneously adopt for the task) but, on
the other hand, detracting from performance in endeavors that require greater item-
specific, feature-based, or analytical attention. Evidence for just such context-depen-
dent effects of a form of values affirmation was recently provided (Schmeichel, Vohs,
& Duke, 2011). Whereas a more abstract orientation (induced by asking individuals to
think about why they pursued an important value) was beneficial on an inhibitory
“stop-signal” task that required both response inhibition and goal maintenance in
working memory, a more concrete orientation (induced by asking individuals to think
about how they pursued an important value) benefited performance on the stop-signal
task when no working memory was required, and instead performance needed to be
guided by the immediate concrete stimulus environment. Stated differently, there was
Impl ications and Appl icat ion s of iC ASA 577
a significant interaction between the level of construal induced (relatively abstract vs.
relatively concrete) and the particular demands of the stop-signal task to be per-
formed, with an abstract construal beneficial for the inhibitory task that required a
form of temporal distancing (keeping track of stimuli on both the current and several
earlier trials) but not for the task that did not demand such temporal distancing.
W H AT A R E T H E N E U R A L M E C H A N I S M S I N V O LV E D I N
T R A N S I T I O N I N G B E T W E E N TO P - D O W N E X E C U T I V E
C O N T R O L A N D T H E “ D E F A U LT M O D E ” A N D H O W D O T H E S E
N E T W O R K S D Y N A M I C A L LY I N T E R A C T I N C R E AT I V E T H O U G H T ?
In Chapter 9, we considered a small portion of the rapidly expanding set of empirical
findings and theoretical accounts relating to the so-called default mode network of the
brain. We saw that there are convergent findings, across multiple methodologies, that
the default mode network includes regions of the medial prefrontal cortex, posterior
cingulate/retrosplenial cortex, and the inferior parietal lobule. We further saw that
this network may include a number of subnetworks, such as a subsystem especially
involved in providing associations and relational information from memory (involv-
ing the hippocampal formation, the posterior cingulate cortex, inferior parietal lobe,
and portions of the medial prefrontal cortex) and a second subsystem (involving par-
ticularly dorsal ventromedial prefrontal cortex) that may be involved in self-relevant
mental simulations or, more generally, in forms of thinking that require one to con-
ceive of others or other things or beings “as being social, interactive, and emotive like
oneself” (Buckner et al., 2008, p. 24). We also encountered differing proposals regard-
ing how the executive control and the default mode networks may interact.
Although the executive and default networks have most often been seen as acting
in opposition to one another, such that when the executive network becomes acti-
vated, the default network becomes deactivated or actively suppressed—or as involv-
ing an extrinsic system comprising areas associated with the processing of external
inputs and an intrinsic system that largely overlaps with the task-negative default-
mode network (Golland et al., 2007)—this view may be somewhat oversimplified. We
saw that Christoff and colleagues (2009) presented evidence that two key regions of
the executive network, including the dorsolateral prefrontal cortex and a dorsal region
of the anterior cingulate, were recruited during phases of “mind wandering” and,
furthermore, that activation in these regions tended to be greatest when participants
were unaware that their minds had wandered from the difficult sustained attention
monitoring task they were supposed to be performing. This raises the important
possibility that, at least under some circumstances, the executive and default net-
works may be recruited in parallel, and it coheres with other findings suggesting that
these networks may not be entirely discrete or that there may be a third system that is
“anatomically interposed between the task-positive and task-negative networks” (Fox
et al., 2009, p. 3281; see Vincent et al., 2008). Shehzad and colleagues (2009) likewise
recently observed that, in cluster analyses, the cluster membership of the dorsolateral
prefrontal cortex with the “task-positive network” was particularly low and that this
region was unique in clustering with the task-positive network in one investigation,
but with the task-negative network in another study.
578 BRAIN AND ENVIRONMENT
More recently, adopting a novel paradigm, Spreng and colleagues (2010) contrasted
the regions recruited during an externally focused goal-oriented visual-spatial
planning task (a visually presented Tower of London task) and an internally focused
goal-oriented task involving self-related autobiographical planning. In the latter
task, participants were asked to plan successive steps to meet different personal goals
(e.g., achieving academic success; traveling). Consistent with previous research, the
visual-spatial planning task engaged regions often recruited during attentional tasks,
including the dorsolateral prefrontal cortex and superior parietal lobule, whereas the
autobiographical planning task engaged the default network. Critically, however, both
the externally directed visual-spatial planning task and the internally directed auto-
biographical planning task engaged the frontoparietal control network, including
anterior insula/frontal operculum, dorsal anterior cingulate cortex, and anterior infe-
rior parietal lobule. As proposed by Spreng and colleagues, these findings suggest that
“the frontoparietal control network may flexibly couple with the default and dorsal
attention networks according to task domain, serving as a cortical mediator linking
the two networks in support of goal-directed cognitive processes” (Spreng et al., 2010,
p. 303, emphasis added). Further articulation of the relations between these large-
scale networks is needed, with direct implications for understanding the neural mech-
anisms that enable us to effectively exercise oscillatory range in levels of control across
tasks that demand our externally focused attention and those that involve predomi-
nantly internalized—but nonetheless goal-guided—cognition.
On a closely related note, we considered the hypothesis that right fronto-insular
cortex and dorsal anterior cingulate cortex may be important in switching between
the central executive and default networks (e.g., Sridharan et al., 2008). We addition-
ally considered evidence that right fronto-insular cortex may assume a causal role by
signaling the salience of a stimulus, together with the more speculative proposal by
Craig (2009a; see also Hakeem et al., 2009) that this region, based on the combination
and integration of multiple forms of saliency maps, ranging from highly internal
interoceptive to motivational, social, and cognitive conditions, is involved in the
representation of the “now” that crucially contributes to a sentient self, leading to a
“meta-representation” of the “global emotional moment.” However, we know com-
paratively little about how, precisely, multiple forms of salience maps interrelate with
one another, in time, to dynamically and effectively guide ongoing behavior,
judgments, and thinking.
Many further questions with respect to the roles and operation of the “default net-
work” in creatively adaptive and flexible thinking remain. For example, how does the
ability to effectively “lose oneself” in one’s work, as shown by attenuation of activity in
the default mode network during full engagement with a task (e.g., Golland et al., 2007;
also compare with our consideration in Chapter 9 of the research by Sheline et al.,
2009, showing a disruption in such capacity in individuals who are clinically depressed),
relate both to the extent to which individuals are able to generate creatively adaptive
alternative perspectives on problems and problematic situations (perhaps because the
default network is allowed to more fully “reset” or “reconfigure” during task engage-
ment) and to changes in subnetworks relating to memory and recollection?
We saw (in Chapter 9) that the preexisting or preceding “neural context” from
which we encounter events and stimuli may markedly influence how those events are
Impl ications and Appl icat ion s of iC ASA 579
processed, such as whether remote associate problems are more or less likely to be
solved through a process of systematic search versus insight (Kounios et al., 2006;
Kounios et al., 2008) or whether a given stimulus is likely to later be forgotten (Otten
& Rugg, 2001; Uncapher & Wagner, 2009). To what extent are such changes in “neural
receptivity” correlated with subjective or introspective evaluations of, for example,
one’s momentary readiness to encounter new information? Can we become “attuned”
to such changes, or to their temporal patterns (cf. Schroeder & Lakatos, 2009), thereby
allowing a better fit between our ongoing task engagements, the need for stimulus
processing, and our neural/neural system’s readiness for them?
Far-reaching implications for how we think about our investigations of the mind
and its activity arise from the apparently simple notion that intrinsic dynamic brain
connectivity that is present before a stimulus occurs itself shapes how that stimulus is
processed and classified and remembered. As remarked by Fox and colleagues (2005),
recognition of the dynamic contributions of the brain’s underlying intrinsic organiza-
tion: “encourages shifting one’s perspective of brain function from the view of a system
simply responding to changing contingencies to one operating on its own, intrinsically,
with sensory information modulating rather than determining the operation of the
system” (Fox et al., 2005, p. 9677). Additionally, as recently observed by Barrett, rather
than thinking about mental causation in mechanistic and linear terms, such as
“Psychological Process A localized in Brain Area 1 causes the separate and distinct
Psychological Process B localized in Brain Area 2, and so on,” from this more probabilis-
tic model we might, instead, think of how: “Brain State A at Time 1 [. . .] makes it easier
to enter Brain State B [. . .] than Brain State C at Time 2” (L. F. Barrett, 2009, p. 334).
This perspective also clearly connects to extensive neurophysiological evidence
relating to ongoing and extensive neuronal oscillations in cortical networks—spanning
five orders of magnitude in frequency (Buzsáki & Draguhn, 2004; for in-depth treat-
ment see Buzsáki, 2006; X. J. Wang, 2010)—and providing a potential mechanism
enabling larger-scale alterations in whole-brain neural connectivities. Such network
oscillations have been shown to bias input selection, to temporally link neurons into
assemblies, and to facilitate synaptic plasticity. Growing evidence suggests that com-
prehending “the coupling of oscillatory activities at different frequencies between brain
regions is crucial for understanding the brain from a functional ensemble perspective”
(C. K. Young & Eggermont, 2009, p. 61; see also Schroeder & Lakatos, 2009).
Long-range phase synchrony of oscillatory neuronal population activity has been
found between multiple regions during tasks such as visual short-term memory main-
tenance, visual object processing, attention tasks, and multisensory integration, and
current evidence suggests that such synchrony can act as a dynamic mechanism sup-
porting large-scale functional interactions in the brain (Bressler & Menon, 2010). In a
recent exploration, episodes of widespread synchrony were found in all frequency
bands, not only before and after external stimuli but also in background EEG, as well
as in both common and average-referenced data (Pockett, Bold, & Freeman, 2009).
These brief episodes of synchrony across the entire head evolved over a period of about
100 milliseconds, and were found in all participants in all pass bands studied, but they
were more common in some bands and were never observed in noise.
Yet, despite many promising advances, the precise role of long-range phase
synchrony in conscious thought is still very unclear (see, for example, Pockett &
580 BRAIN AND ENVIRONMENT
Holmes, 2009), and there are multiple, complex, and complexly interconnected
methodological and empirical issues that constrain interpretation and urge the need
for caution (X. J. Wang, 2010). Understanding the role of long-range synchrony, and
the broader neurophysiological bases of when, and how, we transition between brain
states, will be essential to attaining a deeper understanding of mental agility.
W H AT A R E T H E R E L AT I O N S B E T W E E N T H E S E V E R A L D I F F E R E N T
G R A D I E N T S O F “ R E P R E S E N TAT I O N A L S P E C I F I C I T Y ” T H AT H AV E
BEEN IDENTIFIED IN THE BRAIN, AND HOW DO THEY
D Y N A M I C A L LY C O N T R I B U T E TO T H O U G H T ?
We have considered evidence for an anterior-to-posterior gradient in relation to the
control of actions, with increasingly higher order and more abstract representations
in more anterior cortex (e.g., Badre & D’Esposito, 2007; Christoff, Keramatian et al.,
2009; Koechlin et al., 2003; Chapter 8). We also have reviewed some of the evidence
for a “coarse semantic field” account of hemispheric differences in the processing of
words and concepts, according to which, in contrast to more focused activations in the
left hemisphere, larger semantic fields in the right hemisphere may—with sufficient
processing time—allow weak but remotely associated concepts to become activated,
thereby particularly facilitating such processes as insight and inference (e.g., Beeman,
1998; Beeman et al., 1994; Ben-Artzi et al., 2009; Stringaris et al., 2006; Chapter 9).
How do these two gradients, relating to the level of representational or process speci-
ficity required for action control on the one hand, and for semantic processing on the
other hand, conjointly influence cognition? And how do they relate to evidence for
possible lateralization effects in abstract/categorical versus specific/exemplar object
processing in posterior occipito-temporal cortex?
Specifically, there is both behavioral evidence using the divided visual field paradigm
(e.g., Marsolek, 1999; see also Kensinger & Choi, 2009) and neuroimaging evidence
(e.g., Koutstaal et al., 2001; J. S. Simons et al., 2003; see also Doehrmann et al., 2010) to
suggest that there are two posterior object processing subsystems that may differ in
level of representational specificity: an abstract-category subsystem that operates com-
paratively more effectively in the left hemisphere that is less sensitive to the specific
characteristics of stimuli, and a specific-exemplar subsystem that operates relatively
more effectively in the right hemisphere. According to the dual subsystem account for-
warded by Marsolek and colleagues (e.g., Marsolek, 1999; Marsolek & Burgund, 2008)
whereas the left hemisphere/abstract-category subsystem is relatively more efficient at
analytic or features-based processing and neurocomputation (e.g., Marsolek, 2004), the
right hemisphere/specific-exemplar subsystem is relatively more proficient at holistic or
whole-based processing and neurocomputation. There is also evidence that correspond-
ingly lateralized differences in the amount of activation in right versus left occipitotem-
poral (fusiform) cortex during an individual’s initial encounter with a stimulus are
predictive of subsequent memory performance, with greater activity—at encoding—in
right occipitotemporal cortex predictive of subsequent item-specific rather than cate-
gory-based memory for the stimulus (Garoff, Slotnick, & Schacter, 2005).
But how do differing levels of specificity with respect to how stimuli are perceived
and encoded relate to the forms of conscious and deliberate processing that
Impl ications and Appl icat ion s of iC ASA 581
involving reduced brain activity in posterior cortical regions together with increased
activity in frontal regions in older compared with younger adults, and also to the evi-
dence (introduced in Chapter 10, in the section on “Brain Reserve, Cognitive Reserve,
and Compensation”) of age-related reductions in “neural specificity” across different
object categories (e.g., D. C. Park et al., 2004; J. Park et al., 2010).
Arriving at a more detailed and comprehensive understanding of the ways in which
word comprehension leads to perceptual simulations that are themselves more versus
less detailed, and more versus less vividly “real and concrete” but nonetheless still
“virtual enactments” of objects and actions, promises to provide deep—conceptually
and empirically grounded—understanding of the relations between “words” and
“world.” It will involve refinement of our understanding of how our brains bring
together the diverse and multifaceted aspects of what comprises an individual action
or object, such as the taste, fragrance, weight, name, and other conceptual features of
a grapefruit (see Chapter 8), including articulation of the dynamic interrelations
between multiple neural “convergence zones,” or regions of “multisensory interplay”
(e.g., Doehrmann et al., 2010; Driver & Noesselt, 2008; Talsma et al., 2010) and
whether, indeed, there is one (or more) “amodal hubs,” that are, as it were, “superordi-
nate” convergence zones, or convergences of convergence zones. Fittingly enough, the
efforts to arrive at such an understanding will also increasingly bring together research
aimed to address questions about perception and action, and questions that originate
in problems of language, categorization, and semantics (e.g., Bub & Masson, 2010;
Bub, Masson, & Cree, 2008; Yee, Drucker, & Thompson-Schill, 2010).
W H AT A R E T H E S O U R C E S A N D L I M I TAT I O N S
O F I N T E R V E N T I O N S T H AT M AY C O U N T E R A C T
S E L F - R E G U L ATO R Y R E S O U R C E D E P L E T I O N ?
We now know a great deal of the multiple ways in which self-regulatory resource
depletion may occur, and the many different ways that such resource depletion may
manifest itself (detailed particularly in the second section of Chapter 5). In contrast,
we know much less regarding how to counteract depletion or to replenish self-regula-
tory resources, or of how, and if, our engagements with the world can be interleaved
such that we remain at a near optimal level throughout (“replenishing as we go”). We
also know little about individual differences in how to optimize such alterations. Do
some people tend to naturally or spontaneously structure their days to enable such
near-optimality throughout? Might such “spontaneous structuring” of one’s days and
efforts be an underlying behavioral difference factor that enables some individuals to
be “super-achievers” in creative domains, without apparent accompanying costs to
their physiological and interpersonal well-being? Do individuals differ in their explicit
and implicit understanding of how “aptly” varying their LoC can promote mental
agility? Is such metacognitive knowledge, or perhaps “metaexperiential” awareness,
another frequent contributor to resilience—along with such widely acknowledged
factors as optimism and positive affectivity that we considered in Chapter 6 and
Chapter 9? Conversely, are some individuals perhaps subtly or progressively under-
mining their longer term resilience, and perhaps also forfeiting ongoing opportunities
for creative insight and synthesis, through relentless “on-time” during their waking
Impl ications and Appl icat ion s of iC ASA 583
requires that we relinquish too stringent and too unrelenting self-regulatory control.
We have also seen that, in some contexts, our efforts at control may, paradoxically,
undermine the aims we seek as, for example, in the case of efforts to fall asleep or to
engage in well-practiced skills (e.g., the sections in Chapter 7 on “Trying Not” and
“Absorption, Flow, and ‘Hypoegoic’ Self-Regulation”). Thus, it seems that there may be
circumstances under which the “depletion” that sustained self-regulatory efforts bring
in their wake might yield positive effects.
Here, the recent work by Apfelbaum and Sommers (2009) showing positive effects
of self-regulatory depletion on the interactions of individuals discussing issues of
diversity in an interracial context provides a concrete example. These researchers found
that White participants who had earlier performed a resource-demanding computer
task and then engaged in a conversation with a Black person about diversity issues on
campus reported that they enjoyed the experience more, and they displayed less inhib-
ited behavior. Equally important, they were judged to be less prejudiced by Black observ-
ers than were White control participants who had performed a nondepleting version of
the computer task. On the one hand, studies have shown that, in many cases, prejudice
emerges as a result of failures of self-control, including as a result of resource depletion
(e.g., Govorun & Payne, 2006; Muraven, 2008; Richeson & Trawalter, 2005). On the
other hand, this does not mean that, for all persons and in all contexts, additional self-
control will be beneficial, particularly if self-regulatory efforts are misguided, and
result in overly constrained and excessively closed interaction styles.
It can also be asked if there is an “inverted U” function relating to self-regulatory
resources, such that optimal performance may sometimes arise after utilizing self-
executive control for a moderate (but not too long) period of time. Do “flow” states
(Csikszentmihalyi, 1990, 1996; Keller & Bless, 2008), or phases during which we
become deeply absorbed and engaged in pursuing an activity, with little awareness of
the passage of time and intense attention on an unfolding task, tend to emerge under
such conditions? Increasing research exploring so-called “effortless attention” (Bruya,
2010) and also relating this construct to that of flow (de Manzano et al., 2010) suggest
that some forms of intense task engagement may not inevitably draw on effortful
“top-down” control mechanisms.
H O W S H O U L D T H E D AY - TO - D AY S C H E D U L E S O F I N D I V I D UA L S
A N D G R O U P S B E S T R U C T U R E D TO B E S T A L L O W F O R D I F F E R E N T
L E V E L S O F P R O C E S S I N G C O N T R O L S O A S TO M A X I M I Z E
C R E AT I V I T Y A N D L E A R N I N G ?
A salient example here is a child’s recess during the school day. Pellegrini and Bjorklund
(1997, p. 35) note that “although recess has been part of formal educational systems
since their inception, it is incredibly understudied.” Nonetheless, and “despite the
paucity of empirical guidance for policy decisions, many school systems around the
country are eliminating recess from the curriculum or replacing it with teacher-guided
physical education, based on the belief that it detracts from school’s primary mission:
teaching the Three R’s” (Pellegrini & Bjorklund, 1997, p. 35; see also Panksepp, 1998).
Entirely in accord with these claims, recent analyses of data from more than 10,000
American third-grade children (between the ages of 8 and 9) showed that nearly 30%
Impl ications and Appl icat ion s of iC ASA 585
of the children received either no recess break or only a brief recess of less than 15
minutes during the school day (Barros, Silver, & Stein, 2009). This study also found
that the children not given more than a minimal recess were disproportionately from
lower-income families and from Black and Hispanic ethnic groups.
Other studies likewise show that the amount of free, unstructured time that
American school-age children are given has decreased in the last 20 years (e.g., Ridgway
et al., 2003), including both decreased play and especially decreases in unstructured
outdoor activities. Yet teachers’ ratings of the children’s group classroom behavior
indicated that there was significantly less frequent misbehavior for children who
received at least one break of greater than 15 minutes (Barros et al., 2009). And when
Grade 4 children in a large southern urban school who were not usually given a recess
were given a recess once a week—so that researchers could compare their behavior on
recess and nonrecess days—it was found that the children showed significantly less
fidgeting and more time on task during the postrecess portion of their classes (Jarrett
et al., 1998). These benefits were observed for most of the children, with about 60% of
the children benefiting considerably, and all five of those with attention-deficit disor-
der showing improvements, leading Jarrett et al. (1998, p. 126) to conclude that “for
most children, uninterrupted instructional time may be a paradoxically inefficient use
of instructional time.”
Beyond excessively taxing their executive and self-regulatory resources, long peri-
ods of directed attention during structured class time do not adequately accommodate
children’s natural need for physical activity (e.g., Panksepp, 1998; see also Deslandes
et al., 2009) or individual differences in attentional control (e.g.,Tantillo, Kesick,
Hynd, & Dishman, 2002). Using recordings of daily arm-and-leg movements in indi-
viduals from infancy to 16 years of age, Eaton, McKeen, and Campbell (2001) observed
an inverted U pattern of activity across age. There was a peak in the number of arm
and leg movements per hour found in children of 8 years of age, and gradually decreas-
ing levels observed at both increasingly younger and increasingly older ages. Eaton
and colleagues (2001) postulated that high rates of activity at this age might, in part,
reflect the children’s efforts to draw on concrete objects and interactions with their
environment to facilitate cognition, with the decreases in movement in early adoles-
cence signaling or accompanying a shift toward greater engagement in more abstract,
cognitive activities. Other researchers (e.g., Pellegrini & Bjorklund, 1997) have sug-
gested that recess breaks may help to overcome the buildup of proactive interference
in memory and cognition linked to prolonged periods of learning. Despite these sug-
gestions there is, overall, remarkably little systematic empirical research on the opti-
mal timing and duration of recess for children, or of the conditions under which other
activities, such as teacher-guided engagement in physical activities, provide a suitable
alternative to unstructured time.
We also need to understand more about “adult recess” times—breaks in attention-
demanding work and variations in levels of cognitive control—that can maximally
promote mental agility. What are optimal “in between time” activities, and the dura-
tion of those activities, to help individuals maximize creatively adaptive thinking,
deciding, and acting? Despite the importance of this question, there is comparatively
little sound empirical research, even with respect to such aims as minimizing the risk
of accidents and injuries in industrial settings, though there is some evidence that, for
586 BRAIN AND ENVIRONMENT
example, more frequent, briefer breaks may help to offset fatigue and increase produc-
tivity (P. Tucker, 2003).
One clear potential starting point would be empirical evaluation of proposals, such
as that by Elsbach and Hargadon (2006), briefly alluded to in Chapter 5, of the value
of encouraging “knowledge workers” to intersperse phases of cognitively challenging
and high-pressure work within their work weeks with what might be called “recharge
times.” Such times would comprise phases of work that are low in cognitive difficulty
(e.g., that place minimal demands on directed attention) and are low in performance-
related pressures. Elsbach and Hargadon (2006) argued that “relentlessly mindful
work,” particularly work that exerts continuous demands on such core job dimensions
as skill variety and autonomy, if combined with high workload pressure (e.g., multiple
and often unpredictable time demands and deadlines, and multiple complex projects
with differing time horizons), could undermine the ability of individuals to experience
the positive psychological states that, in turn, foster and sustain creativity—such as
high levels of experienced meaningfulness of work, knowledge of the actual results of
work activities, and experienced responsibility for work outcomes.
Figure 12.1 provides a schematic of the hypothesized effects of such “relentlessly
mindful work.” The figure is a modification of an earlier model of job characteristics
developed by J. R. Hackman and colleagues (1975), indicating (with the “broken arrows”)
the potentially weakening effect of high workload pressure on the connectivity between
Critical Personal
Implementing Core job High psychological and work
concepts dimensions workload states outcomes
pressure
core job dimensions, such as skill variety and task significance, and emergent critical
psychological states, such as experienced meaningfulness of work and experienced
responsibility for work outcomes.
To overcome such chronic workload pressures, Elsbach and Hargadon (2006) recom-
mend the use of “legitimate and scheduled mindless work.” Figure 12.2 schematically
depicts the hypothesized benefits of interposed phases of “mindless work”—that is, com-
paratively brief periods of time during which individuals work on easily mastered, rou-
tine, or automatically accomplished but nonetheless “productive” tasks (e.g., filling supply
cabinets, performing routine maintenance, or cleaning of equipment). Such times could
“allow professionals to experience breaks from their chaotic mindful work to allow them
to feel a sense of predictability and control, as well as to provide them with the cognitive
capacity to work creatively on other problems” (Elsbach & Hargadon, 2006, p. 480).
Additionally, as shown in Figure 12.2, such recharge times are hypothesized to elicit
critical psychological states such as high cognitive capacity, psychological safety, and pos-
itive affect. Brief “recharge times” of this form might also provide opportunities for the
incubation of ideas, given evidence (e.g., Sio & Ormerod, 2009), considered in Chapter 7,
that incubation may be particularly likely to occur in phases of low cognitive load.
In a conceptual analysis, Jett and George (2003) differentiated between several
forms of interruptions that may be experienced in the work environment, including
intrusions, breaks, distractions, and discrepancies. They identified each as, depending
on circumstances, leading to either, or both, positive and negative consequences for
the person being interrupted. Whereas, for instance, breaks may lead to costs in time
spent relearning essential details of the work being performed, they may also provide
opportunities for incubation of ideas (e.g., see the section on “Working Well with the
Unconscious” in Chapter 7). Breaks may provide the opportunity for both passive
Critical Personal
Implementing Core job
psychological and work
concepts dimensions
states outcomes
Responsiveness breeds the need for more responsiveness. When people are
“always on,” responsiveness becomes ingrained in the way they work,
expected by clients and partners, and even institutionalized in performance
metrics. There is no impetus to explore whether the work actually requires
24/7 responsiveness; to the contrary, people just work harder and longer,
without considering how they could work better. Yet, what we discovered is
that the cycle of 24/7 responsiveness can be broken if people collectively
challenge the mind-set. Furthermore, new ways of working can be found
that benefit not just individuals but the organization, which gains in quality
and efficiency—and, in the long run, experiences higher retention of more of
its best people. (Perlow & Porter, 2009, np)
vacations (more than 10 days) showed similar effects on stress and burnout, suggest-
ing that multiple short vacations might be more beneficial than one longer annual
vacation. Nonetheless, although these studies are suggestive and encouraging, overall
there is very little rigorous research on the effects of vacations. Particularly needed is
investigation of the moderators of vacation effects, involving appropriate control
groups and also utilizing multiple within-person physiological, psychological, and
behavioral measures that would permit comprehensive objective evaluation.
Other promising directions with regard to the question of opportunities for revi-
talization of attention and other cognitive resources that contribute to resilient and
adaptive functioning are provided from the perspective of “attention restoration
theory” (S. Kaplan, 1995, 2001), and the broader but closely related account of Ulrich
(1993; Ulrich et al., 1991, 2008). As we have seen, Ulrich has hypothesized that
certain natural settings—specifically those that have been evolutionarily favorable to
our ongoing well-being and survival, such as grassland savannah-like spaces—may
help to rapidly offset stressors, shifting us toward a more positively toned emotional
state, counteracting stress-induced mobilization of the sympathetic nervous system,
and influencing attention, conscious processing, and behavior. (See Chapter 11; see
also the discussion of “virtue regrets” versus “indulgence regrets” in Chapter 5, in the
section on “Levels of Control, Spontaneity, and Openness to Experience”). The theory
of “allostatic load” (e.g., McEwen, 2008) in relation to stressors (discussed in Chapter
10 in the section “Socioeconomic Status, Stress, and Brain Paths to Agile Thinking”)
also provides conceptual guidance here (e.g., Geurts & Sonnentag, 2006). As noted
earlier, allostatis can be viewed as the “active process by which the body responds to
daily events and maintains homeostasis” or is able to achieve “stability through
change,” whereas allostatic load refers to “the wear and tear that results from either too
much stress or from inefficient management of allostatis” (McEwen, 2008, p. 175).
Sluiter and colleagues (2000) have distinguished different time-scales of recovery
from demanding or stressful work based on the duration of the respite and time since
work was discontinued. They differentiate four temporally based categories that cor-
respond to the way in which working life is organized in many countries: microrecov-
ery (the first minutes after task performance), mesorecovery (10 minutes to 1 hour
after task performance), metarecovery (1 hour to 2 days after work, with the upper
end of the range such as might be true for a weekend), and macrorecovery (more than
2 days after work). Based on a review of studies that examined neuroendocrine reac-
tivity and recovery from mental, combined mental and physical, or physical tasks, and
including occupational, health, laboratory, and sports research, Sluiter et al. (2000)
suggest that there are important parallels between findings on sports related over-
training and that of people with occupationally induced chronic fatigue.
Although research on the neuroendocrinology of occupational tasks greatly lags
behind that found for sports activities, outcomes suggest that, depending on circum-
stances, parallels to both overtraining of the sympathetic nervous system and of the
parasympathetic system may be observed. The former may be characterized by, for
example, increased sympathetic activity at rest, such as increased resting heart rate,
decreased appetite and weight loss. The latter may be characterized by decreased sym-
pathetic and increased parasympathetic activity involving, for example, low resting
heart rate, more hours sleeping, and a “phlegmatic” or depressive state.
590 BRAIN AND ENVIRONMENT
It is thus arguable that if a worker’s response to acute work stress and fatigue
includes a progressive reduction in exercise and creative and social activities,
there is a commensurate loss of important sources of personal fulfillment,
which might otherwise stimulate the release of pleasure-reward neurotrans-
mitters with their stress-reducing, allostatic load-opposing potential. This
behavioral change may lead to a prolongation of work stress spillover effects
Impl ications and Appl icat ion s of iC ASA 591
attention and cognition but also our health, productivity, and ultimately our creativity
and adaptive flourishing. Here, as so often, William James both recognized, and artic-
ulated for us, something that is so simple and so fundamental, that we need to remind
ourselves of it, and others too.
The fact is that every man who possibly can should force himself to a holiday
of a full month in the year, whether he feel like taking it or not. First, for the
reason we have considered hitherto—that the capacity for irresponsible
enjoyment which is like air space in the character, may not become wholly
atrophied within him—though many cannot and many will not treat this as
a “practical” reason. But second, for the reason that all must consider practi-
cal, namely, tone of mind and health of body. No man, were he composed of
catgut and whalebone, can work for five years unremittingly at the same
kind of work with impunity. None can work ten years even at a very varied
occupation. One year may make no difference, a second and a third may
follow, and the subject not suffer consciously. But ten years of the two sys-
tems will turn out two different human beings at their end. The patient may
be loth to get away, but this is a distinctly morbid symptom, a cramp-like
closure of the mind upon the subject of its cares, which should be an impera-
tive signal to some friend to come and push him willy-nilly out of doors.
(William James, 1873/1987, pp. 4-5)
W H AT A R E T H E R E L AT I O N S B E T W E E N D I R E C T E F F O R T F U L
“AT T E N T I O N T R A I N I N G ” I N T E R V E N T I O N S A N D L E S S D I R E C T E D
I N T E R V E N T I O N S S U C H A S M E D I TAT I O N , M I N D F U L N E S S
T R A I N I N G , A N D AT T E N T I O N R E S TO R AT I O N ?
In a recent review, Tang and Posner (2009, pp. 222–223) contrasted what they termed
“attention training” methods, involving “practice in some cognitive skill by repetitive
trials on tasks similar to those used in schools or cognitive psychology laboratories”
versus “attention state training” interventions that “have in common an altered state
of mind and body” but “use different sensory inputs to achieve their effects on mind
and body and improve performance.” Examples of “attention training” methods that
we have considered (see Chapter 11) include the attention training of children exam-
ined by Rueda et al. (2005), the dual-task variable-priority training and real-time
video gaming examined by researchers such as Kramer et al. (1995) and C. S. Green
and Bavelier (2003, 2006), respectively, and the multimodal working memory training
used by Jaeggi and colleagues (2008). In contrast, “attention state training” interven-
tions that we have considered include the “attention restoration” manipulations based
on S. Kaplan’s (1995, 2001) theory, such as engagement with nature (Chapter 11), and
mindfulness training or integrative body-mind training (discussed in the first section
of Chapter 3).
In contrasting these two approaches, Tang and Posner (2009) emphasized differ-
ences on five aspects. Specifically, they underscored that attention training versus
attention state training can be contrasted with respect to the immediate effects of the
Impl ications and Appl icat ion s of iC ASA 593
ultimately be ideal. Yet, if so, how much movement toward the endpoints, and for how
long, and under what conditions is ideal?
and almost a caricature of the task. Very often, if we’d only get started, we will find
that many imagined difficulties disappear or that the solutions to them emerge
through the broad and diverse support provided by reimmersion in the relevant
physical and symbolic context.
We need to encourage individuals who are learning a new domain, or are experienc-
ing overly abstract and global fears and anxieties regarding how to move forward with
respect to a given problem (e.g., “writer’s block”), to recognize that their mind and the
“representational accessibility landscape” that they are in when they are remote from
actually working on a given problem is markedly different than when they are
immersed in the problem context, and have at hand myriad contextual cues from the
environment and from their own interactions with the environment. There is a much
(much!) wider range of information and many more possibilities that will be “ready to
mind” once one becomes immersed in the appropriate problem-solving context, which
allows processes such as automatic reminding and the triggering of “if-then” rules and
so on to come to the fore and “share the load” of thinking with our conscious and
deliberate efforts at control. As noted by Guindon:
These points also interlink with the notions of the benefits of being able to flexibly
shift between “making” versus “finding” depending on context and other demands, so
that aims become something that have multiple origins, in our selves and in what the
world offers (see Chapter 7, particularly Excursion 7, “Goals, Making and Finding, and
Oscillatory Levels of Control”).
Although, to date, considerable (and rapidly growing) research effort has been
directed at evaluating the benefits of direct “training” approaches to compensate for
age-related losses in such domains as memory and fluid reasoning, comparatively less
research has been directed at determining the benefits of intervention approaches
that provide more natural, multimodal, complexly meaningful opportunities—and
self-reinforcing ongoing invitations—to sustained cognitive, socioemotional, and
physical activities that will preserve, foster, and fuel ongoing capacities in all those
domains. As underscored by Stine-Morrow:
and greenery in urban areas may yield considerably more than “merely cosmetic”
benefits.
W H AT F O S T E R S I N D I V I D UA L I S M A N D “ U S E F U L VA R I AT I O N ”
IN OUR HABITS OF THOUGHT AND ACTION?
The philosopher Josiah Royce—a long-time friend and philosophical antagonist
of William James—asked this question in 1898 and suggested that both an induce-
ment to try to vary as well as greater self-criticism and evaluation of what one
produces in response to that attempt to vary was important . . . “What sort of influ-
ence is it that puts the individual on his mettle, that awakens him to valuable
and independent variability of habit, that, as they say, makes him let himself go”?
(Royce, 1898, p.124)
One tremendously overlooked impetus for innovative behavior is—as we saw in
Chapter 5—reinforcement for varied behavior. We considered how such reinforce-
ment might apply at the level of the individual (e.g., in children), and we saw examples
of animals (e.g., dolphins) also learning to creatively respond in accordance with a
“rule” that only the generation of novel, not previously performed, behaviors would be
rewarded. However, “learning to vary” may also apply at the level of the group or orga-
nization. For example, S. Kaplan and Henderson (2005) argue that, in organizations,
incentives and cognition coevolve: “organizational competencies or routines are as
much about building knowledge of ‘what should be rewarded’ as they are about ‘what
should be done.’” Furthermore, they propose that recognizing the common coevolu-
tion of incentives and cognition can lead to important insights into the sources of
“organizational inertia” in the face of changing environments (S. Kaplan & Henderson,
2005, p. 509). Similarly, Simsek (2009) provides a conceptual review of the multiple
factors that may contribute to “organizational ambidexterity” involving a close bal-
ance between what has been termed “exploitation” and “exploration.” As concisely—
and incisively—characterized by March (1991):
Also important here is the notion of a “behavioral cusp” that has been developed by
Rosales-Ruiz and Baer (1997; see also Hixson, 2004), in which repeated cycles of
reinforcement and selection of behaviors lead to cumulative-hierarchical learning.
To take one specific example, learning to walk enables a child to gain access to a new
array of reinforcers that then further develops his or her behavioral repertoire.
Behavioral cusps are those that expose an individual’s “repertoire to new environ-
ments . . . new contingencies, and new communities of maintaining or destructive
contingencies” (Rosales-Ruiz & Baer, 1997, p. 534).
More recently, R. Epstein, Schmidt, and Warfel (2008) have proposed and provided
evidence in support of the notion that creative expression in individuals can be accel-
erated through strengthening any of four basic competencies: capturing (preserving
new ideas as they occur, finding places and times where new ideas can be observed
easily), challenging (taking on difficult tasks, setting open-ended goals, and managing
fear and stress associated with failure effectively), broadening (seeking knowledge and
skills outside one’s current areas of expertise), and surrounding (changing one’s physi-
cal and social environments regularly, seeking out new unusual stimuli or combina-
tions of stimuli). Each of these basic competencies (even if not explicitly named) has
been underscored at various points in the previous chapters—see, for example, the
discussion of the “broaden and build” theory of positive emotion, and of openness to
experience, interest, curiosity, and variety seeking in Chapter 6, the role of epistemo-
logical beliefs and of intolerance of uncertainty versus intolerance of ambiguity treated
in Chapter 7, as well as all of Chapters 10 and 11 regarding how our environments
may, or may not, promote “brain paths” to mental agility.
powerful summary of Andy Clark (2001, p. 132), earlier considered in Chapter 4, pro-
vides a superb reminder on multiple fronts that bears repeating:
The brain’s role is crucial and special. But it is not the whole story. In fact, the
true (fast and frugal!) power and beauty of the brain’s role is that it acts as a
mediating factor in a variety of complex and iterated processes which continually
loop between brain, body and technological environment. And it is this larger
system which solves the problem. […] The intelligent process just is the spa-
tially and temporally extended one which zig-zags between brain, body and
world. (A. Clark, 2001, p. 132)
The question of how can we better put to use our understanding of the intermeshed
nature of representations—in the mind, the world, and our bodies—to best enable
agility of thought and action is vast, with potential implications and applications
across virtually all areas of our lives. Nonetheless, four specific examples where
remaining or again becoming cognizant of these interdependent relations could help
to guide us toward greater agility of mind can provide anchors here (see also, for exam-
ple, Kirlik, 2006).
First, as we have seen, there is clear evidence that encouraging a view of intelli-
gence as malleable and subject to incremental change can be highly beneficial in
encouraging persistence and learning (Chapter 7). What, then, are the effects of
explicitly encouraging a view of intelligence as a joint product of a person’s mind/brain
and the environment that he or she has set up or chosen in which to work or play? Can
emphasizing the interrelations between the ease with which we can think and attend
and the particular environments that we are in, help to guide children—and adults—
to structure physical and symbolic space in more optimal ways, to enable creatively
adaptive thinking?
Second, research efforts could more fully explore ways to put the environment, and
environmental cuing, to “work” for individuals. For instance, the tendency of indi-
viduals with frontal lobe lesions, and also of other patients such as some persons with
traumatic brain injury, to be overly guided by habitual or automatic responses to envi-
ronmental cues may—under the right conditions—actually be adapted to help them.
Specific condition-to-action cues could, for instance, be used to help individuals to
improve their daily planning abilities and initiation (cf. Cicerone, Levine, Malec, Stuss,
& Whyte, 2006), through the thoughtful and imaginative preplanning of specific
prompts and prods to initiate activities. Additionally, as noted in Chapter 5, develop-
ing specific implementation intentions may be a powerful means to counteract the
pull of a well-established habit, placing a different mode of “automaticity” against a
habitually cued goal or behavior, to decrease the likelihood that the new intention is
derailed by the older habitual response. This approach may also lead to improved
memory for intentions in individuals who experience difficulties with deliberate con-
scious remembering, but not with relatively automatic forms of processing, such as
some older adults (e.g., Chasteen, Park, & Schwartz, 2001; Jacoby, Jennings, & Hay,
1996). As noted previously, older individuals who were given guidance in how to use
such “implementation intentions” showed improved prospective memory in a realistic
600 BRAIN AND ENVIRONMENT
fluid thought (such as those we explored earlier in Excursion 2) and to deepen our
level of “attunement” to the sorts of moments that may signal to us new opportuni-
ties, directions, or insights? Should workplaces provide more opportunities for “ludic”
activity?
We need to be alert for, and to take seriously, those moments in which we realize
that we are making a connection to deeper experiences, that are of our felt and
sensed—not “only thought” or coolly cognized—responses to the world around us.
Such moments are those, as the poet Seamus Heaney describes with regard to a par-
ticular moment of his own writing, long (long) before he was and knew he was, a poet.
A moment that was different in just this way:
I had no particular gift for writing what were called “compositions,” and no
particular enjoyment of it. But I do remember a moment, early on at
St Columb’s, when the topic was “A Day at the Seaside” and I made a connec-
tion between the performative student in me and a more inward creature,
the writer-in-waiting, if you like. In the middle of the list of usual, expected
activities such as diving and swimming, neither of which I could do, I wrote
about going into an amusement arcade to escape from a shower and being
depressed by the wet footprints on the floor and the cold, wet atmosphere
created by people in their rained-on summer clothes. This had actually hap-
pened to me, so the image and the recording of it had a different feel.
Something in me knew that I was on the right, intimate track—but it took
me years to follow up. (Heaney, in O’Driscoll, 2008, pp. 35–36)
Mental agility will more often and more strongly emerge if we can recognize such
moments when we’re “on the right, intimate track”—a pathway that is forged not by
our mind alone, but by our minds intersteeped and copenetrated with the world,
through our senses, and as we, as physical (embodied), emotional, and “interest-
pierced” beings, try to navigate that world.
H O W C A N W E B E T T E R U N D E R S TA N D T H E O R I G I N S O F
R E P E T I T I V E A U TO M AT I C T H O U G H T S A N D O V E R LY V E R B A L -
L I N G U I S T I C P R O C E S S I N G A N D T H E I R E F F E C T S O N F L E X I B LY
C R E AT I V E P R O B L E M S O LV I N G ?
Findings from different domains, such as research on clinical depression, and chronic
worry and rumination, point to the potential costs of modes of thinking that are too
exclusively abstract or verbal-linguistic, and, furthermore, that reduced specificity of
autobiographical memory may contribute to impediments in flexibly creative problem
solving (Chapters 2 and 3). Partially similar patterns may be observed in other popula-
tions. For instance, recent findings suggest that individuals with avoidant, dependent,
or obsessive-compulsive personality disorders show markedly reduced memory speci-
ficity compared with nonclinical controls, with more moderate increases in overgener-
ality of memory (Spinhoven et al., 2009). There is also evidence that modes of
rumination may characterize forms of psychopathology beyond depression and worry,
such as eating disorders (e.g., Rawal, Park, & Williams, 2010).
602 BRAIN AND ENVIRONMENT
then be “more vulnerable to the chain of events leading from negative childhood
life events through generalized autobiographical memory and poor interpersonal
problem solving to suicide attempts” (Arie et al., 2008, p. 27).
With respect to the development and maintenance of rumination, evidence that
recurring ruminative thoughts may not be uniquely or exclusively tied to emotional
processing, but may reflect more global mental inflexibility in “trait ruminators”
(Davis & Nolen-Hoeksema, 2000; Whitmer & Banich, 2007, 2010), with rumination
being a “manifestation of a more general tendency toward cognitive inflexibility, or
perseveration” (Davis & Nolen-Hoeksema, 2000, pp. 700–701, see also note 7 in
Chapter 2) likewise suggests the need to take into account additional factors. The role
of other possible “benefits” or potential adaptive aspects of rumination (e.g., Watkins,
2008) similarly merits further exploration, as in the recent work of Altamirano and
colleagues (2010) showing that rumination was associated with enhanced goal main-
tenance on a task that required continued adherence to a single goal in the face of
distraction, but was detrimental in a task that required rapid and flexible movements
between goals.
In line with the multicomponent model of overgeneral memory and impaired prob-
lem solving, there is also evidence that depressive rumination may reflect deficits in
the central executive process of cognitive inhibition (Joormann, 2010) such that
depressed individuals and those at risk of depression have particular difficulty in pre-
venting negative material from entering and remaining in working memory, leading
to rehearsal and elaboration of negative content, and also undermining attempts at
processing new information that might allow for more effective emotion regulation.
For example, Bernblum and Mor (2010) found that brooding rumination, in particu-
lar, was associated with impaired “refreshing” of memory—an aspect of memory
updating that involves briefly thinking back to a just-activated thought or percept (M.
K. Johnson, 1992; M. K. Johnson et al., 2005). For brooding ruminators, impaired
refreshing was found not only following task-relevant, but also for task-irrelevant,
emotional words (cf. M. K. Johnson et al., 2006). Neuroimaging findings such as those
of Siegle et al. (2007) showing that self-reported rumination was related both to sus-
tained activity in the amygdala following challenge (with amygdala remaining acti-
vated throughout nonemotional processing trials for depressed but not control
participants), and to hypoactivity in dorsolateral prefrontal cortex, likewise point to
inefficient “top-down” regulation of emotion (see Banich et al., 2009; Ochsner &
Gross, 2005, for review).
Interventions that aim to counteract rumination by encouraging greater concrete-
ness and specificity in thinking (Watkins et al., 2009) and training in memory specific-
ity (Raes et al., 2009) were noted in Chapter 2, and the potential benefits of mindfulness
interventions in reducing habitual responding and improving executive attention—in
both depressed and healthy individuals—were highlighted in Chapter 3. In other
recent work, Heeren, Van Broeck, and Philippot (2009) found that, compared to
matched controls, mindfulness-based cognitive therapy in a mixed community adult
sample was associated with pre- to postintervention increases in autobiographical
memory specificity, decreased overgenerality of autobiographical memory, and
improved cognitive flexibility, as assessed by category, letter, and verb fluency tasks;
furthermore, the changes in overgeneral memory were partially mediated by the
effects on the cognitive flexibility measure.
604 BRAIN AND ENVIRONMENT
perhaps associated with activity in the default mode network, and a more “immediate,
agentic ‘I’ acting in the present moment,” perhaps associated with right-lateralized
exteroceptive somatic and interoceptive insular cortices. (See the discussion of the
frontal anterior insular cortex in Chapter 9, particularly the proposal that this region
“plays a critical role in interoceptive awareness of both stimulus-induced and stimu-
lus-independent changes in homeostatic states;” Sridharan et al., 2008, p. 12572; also
see Craig, 2002, 2003, 2009a, 2009b).
Specifically, Farb and colleagues hypothesize that there may be “a fundamental
neural dissociation in modes of self-representation that support distinct, but habitu-
ally integrated, aspects of self-reference”:
Additional efforts to explore the differences between these and other modes of
self-reference may help to inform our understanding of when self-reflective thinking
is adaptive and when, instead, it may lead to spiraling detrimental effects that pro-
gressively undermine an individual’s ability to optimally—adaptively and creatively
and with the full use of her or his executive and attentional resources—respond to
new challenges and setbacks.
How we approach positive emotion is also important (Chapter 6). Treatments of
mindfulness characteristically emphasize the importance of “being present.”
Rumination and worry also may be exacerbated by “low savoring” of positive events.
Variability or what has been termed “regulatory diversity” in how one makes the most
of positive experiences was recently found to specifically enhance overall subjective
happiness: “the happier participants were the ones that typically savored various situ-
ations using various strategies” (Quoidbach, Berry, Hansenne, & Mikolajczak, 2010,
p. 371) rather than consistently adopting only a few specific approaches. These find-
ings are in line with other evidence that has underscored the key role of flexibility in
both biological and psychological processes in sustaining well-being. Especially illus-
trative here are the findings of Bonanno and colleagues (2004; see also Coifman &
Bonanno, 2010; Westphal, Seivert, & Bonanno, 2010) that, even after controlling for
levels of initial distress, both the ability to express emotions, and to suppress emotions,
in response to changing experimental requirements (i.e., “expressive flexibility”), was
predictive of longer term adjustment of undergraduate students living in New York
City in the 2 years immediately after the September 11th terrorist attacks.
Drawing upon the growing research literature relating to the differing effects of
positive versus negative affect on attention and cognition, particularly evidence that,
606 BRAIN AND ENVIRONMENT
as we saw in Chapter 6, positive affect tends to promote exploration and social interac-
tions, and modes of approach such as playfulness, enquiry, interest, flexibility, and
creativity, Tarrier (2010) recently developed a cognitive-behavioral intervention
termed the “broad minded affective coping” procedure. The procedure aims to elicit
positive emotion in individuals through encouraging and guiding the detailed recol-
lection and imaging of positive past memories. The technique involves guided imagery
of positive memories, with particular prompts for engaging various senses (e.g.,
sounds, smells, touch, or sensation) and encouragement to reexperience the associ-
ated emotion. Afterwards, the patients are helped to “interrogate” the memory and
their experience, so as to become aware of the associations between memory, their
modes of cognition and appraisal with respect to the events, and emotion. Individuals
are encouraged to practice such recollection both within further treatment sessions
and independently and to recall a variety of different positive memories.
The rationale provided to individuals for this approach of recalling and reexperi-
encing memories with positive affect, is multipronged, but straightforward, with
elements relating to mindfulness and responsiveness to the particular sensory-
perceptual aspects of experience, cognitive appraisal (and reappraisal), and simple
information about how cognition and affect interact with one another and also with
motivation and action. For instance, patients are told that often negative emotions,
such as fear, depression, anger, or shame, are threat-related and that they serve to
focus and narrow attention to remain vigilant or aware of potential threat—raising
the possibility that “the constant experience of negative emotions creates a mental,
tunnel vision.” In contrast, positive emotions are characterized as eliciting a broader
and more varied and variable range of responses such as curiosity and creativity. Such
increasing emphasis on interventions that are aimed to facilitate positive emotions,
rather than only countering negative affect (see Garland et al., 2010, for recent review),
combined with efforts to more specifically train attention and executive control
through mindfulness and other attention-training interventions within domains such
as clinical therapy (e.g., Siegle, Ghinassi, & Thase, 2007), are very promising. Similarly
encouraging are efforts to employ pretrauma/prestress preventive interventions that
may enhance executive control and emotional positivity as a buffer against upcoming
times of high physical, psychological, and emotional duress (Jha et al., 2010). Each of
these are very welcome steps toward more balanced, powerful—and more fully
equipped—interventions for promoting optimal psychological flexibility (Kashdan &
Rottenberg, 2010) and agility of mind.
modified and increased (e.g., Blackwell, Trzesniewski, & Dweck, 2007; Dweck &
Leggett, 1988; Mueller & Dweck, 1998). We have seen an array of evidence document-
ing the considerable benefits to multiple forms of adaptive learning and persistence
that arise from encouraging an incremental view of intelligence. We have also consid-
ered further pervasive effects of our epistemological beliefs on thinking and acting
(particularly considered in Chapter 7). These findings have clear, direct, and profound
implications for formal education and for the practice of teaching. But are there also
other domains, beyond general education, where interventions aimed to challenge
entity construals and to promote incremental construals of the mind and of intelli-
gence might be highly effective in fostering greater cognitive flexibility and openness
to change and growth? A recent demonstration that exposing adolescents to an incre-
mental view of the mind’s abilities helped to alleviate school-related anxiety in indi-
viduals with generalized anxiety disorder (Da Fonseca et al., 2008) is an excellent
example of the forms of application and extension that might be undertaken. It is also
consistent with other research in domains such as cognitive-behavioral therapy and
mindfulness training interventions (for example, as considered in the first section of
Chapter 3), showing the importance of teaching individuals to challenge negative
thoughts that underlie problematic behaviors and thinking.
Incremental versus entity views have also been explicitly linked to whether indi-
viduals will undertake behaviors that are remedial of a problem or problematic situa-
tion (e.g., extra review of a concept or procedure that one has not learned or mastered
by one’s initial attempts) versus behaviors that, instead, primarily defensively shield
one from recognizing or emotionally and psychologically acknowledging the problem
(Nussbaum & Dweck, 2008). A differential tendency to engage in remedial behaviors
versus defensive behaviors—stemming in part from views regarding whether intelli-
gence is malleable versus fixed, and also from other beliefs about the nature of knowl-
edge and learning, such as that learning is “all or none”—if undertaken repeatedly and
over the longer term, would widen the achievement and knowledge gap between indi-
viduals or groups. Those with an incremental view would be more likely to overcome
identified shortcomings in their knowledge and skills, and to substantially extend
their competencies. Persons with an incremental view might set in motion an upward
“broaden and build” cycle, rather than a downward spiral of increasing lack of motiva-
tion and involvement, such as may accompany a fixed view of intelligence or ability,
with accompanying tendencies to avoid confronting apparently unalterable shortcom-
ings or to downplay their importance.
We have clear evidence regarding the potential “snowball” efficacy of interventions
such as self-affirmation (e.g., G. L. Cohen et al., 2006; see Chapter 6). Recent follow-up
findings show that self-affirmation may interrupt a recursive cycle—leading to effects
on measures such as school grade-point average and whether individuals are assigned
to remedial classes or, instead, to advanced math placement, as long as 2 years later (G.
L. Cohen et al., 2009; see also the brief “social belongingness” intervention with minor-
ity college students developed by Walton & Cohen, 2011). However, we need additional
systematic evaluation of these and similar interventions in different contexts, includ-
ing the proposal that the performance of individuals, and their psychological trajec-
tory, “can be strongly influenced by timely actions, even when apparently small, that
alter or reset the trajectory’s starting point” (G. L. Cohen et al., 2009, p. 403).
608 BRAIN AND ENVIRONMENT
A R E T H E R E O R G A N I Z AT I O N A L A N D G R O U P “ S T R U C T U R A L ”
G U I D E S A N D S A F E G UA R D S T H AT M I G H T B E A D O P T E D
TO E N C O U R A G E G R E AT E R A D A P T I V E O S C I L L ATO R Y
RANGE IN LOS AND LOC?
In Chapter 5, we noted that the adoption of an implementational mindset may shift
us in “representational space,” such that we may become especially attuned to the fac-
tors that are relevant to the action and will tend to adopt a positively biased view of
the “situational affordances” for accomplishing the hoped-for goal (Gollwitzer &
Kinney, 1989; S. E. Taylor & Gollwitzer, 1995). Our sensitivity to the effects of imple-
mentation versus deliberative mindsets, and particularly how an implementational
frame may constrain our level of representational specificity, suggests that it may be
beneficial to deliberately plan for (or require) periods of deliberative reevaluation
during the course of larger scale projects. Deliberative reevaluation phases might be
interposed at more natural “choice points” in the development of a project. At these
times, the explicit aim would not be to implement further steps, but to reevaluate and
if necessary reorient and rethink planned directions and goals. Planned deliberative
pauses of this form may also help to offset common decision making and other orga-
nizational dangers, such as “sunk-cost effects” or “mission creep.”
In some contexts, individuals or groups deliberately request that someone take on
the role of the “healthy skeptic” or of the “devil’s advocate,” in an effort to explicitly
encourage the identification and voicing of contrary evidence and viewpoints. It may
be that in some situations someone could similarly take on the role of a “metacogni-
tive” monitor for the group’s or project’s trajectory with respect to LoS and/or LoC in
different tasks or task aspects. If optimizing mental agility requires that we show
appropriate oscillatory range in our LoS and our LoC, can we “offload” at least a small
part of the effort that may be required to prompt appropriate variations in level of
specificity and level of control to institutional or organizational procedures or
guidelines? In addition to a “healthy skeptic,” might we partially formalize the roles of
Impl ications and Appl icat ion s of iC ASA 609
H O W C A N T H E i C A S A F R A M E W O R K H E L P TO I N F O R M O U R
T H I N K I N G A B O U T E T H I C S A N D VA L U E S ?
We have seen many compelling illustrations of the vulnerability of our thinking and
information processing to “self-regulatory resource depletion” (Chapter 5), as shown
by such measures as significantly decreased persistence in simple motor or puzzle-
solving tasks, or diminished likelihood of appropriately inhibiting a strong habitual
tendency to respond in a way consistent with an often-made response. However,
several studies also have examined the possible costs of sustained efforts at self-
regulatory control on the performance of such morally relevant behaviors as ostensi-
bly volunteering to help the victim of a recent tragedy (DeWall, Baumeisteer, Gailliot,
& Maner, 2008), an individual’s tendency to respond violently to provocation by an
intimate partner (Finkel, DeWall, Slotter, Oaten, & Foshee, 2009), and dishonestly
inflating the amount of payment to be received for “correct” answers on a general
knowledge task (Mead, Baumeister, Gino, Schweitzer, & Ariely, 2009). The findings
from these studies have closely paralleled those found with more strictly cognitive or
non-ethically relevant behaviors, suggesting that behaviors that have ethical and
moral dimensions are likewise potentially vulnerable to disruption through condi-
tions that deplete self-regulatory resources.
Equally important, however, we have also seen that whether or not self-regulatory
failures are likely to occur is not simply a matter of the degree or number of self-
regulatory challenges we have recently faced: Self-regulatory success is moderated by
such factors as our beliefs or implicit theories about the nature of willpower (Job,
Dweck, & Walton, 2010; Chapter 5; cf. Bandura et al., 2001), the predominant level of
construal or action identification that we adopt as influenced by such factors as self-
affirmation (Schmeichel & Vohs, 2009; also see Wakslak & Trope, 2009; Chapter 6),
and the extent to which we perceive our actions and choices as self-determined as well
as our experienced autonomy in the actions we undertake (Muraven, Gagné, &
Rosman, 2008; Chapter 5). Additionally, and also of equal importance, we have seen
that, with experience, we can become more or less practiced and proficient at self-
regulatory control, with sustained training in self-regulatory control leading to
improved performance on self-control tasks and attenuated self-regulatory depletion
(e.g., Gailliot, Plant, Butz, & Baumeister, 2007; Muraven, 2010; Oaten & Cheng, 2007;
see Hagger et al., 2010, for meta-analytic findings; Chapter 5 and Chapter 11).
Taken collectively, these findings urge us to exercise particular care in the expres-
sion of claims about the processes that support or undermine successful self-regula-
tory control in our choices and actions, including those that may have ethical import.
610 BRAIN AND ENVIRONMENT
As succinctly noted by Job, Dweck, and Walton (2010, p. 1692), “It is important that
people understand that their own beliefs about willpower as a limited or nonlimited
resource can affect their self-regulation. It is also important that psychologists
appreciate the impact of powerful and widely shared lay theories about the self and
distinguish their effects from seemingly immutable biologically driven processes.”
These findings also prompt us to recall some further advice of William James—the
same William James who, as we saw earlier, strongly recommended the regular taking
of holiday breaks to sustain our “tone of mind and health of body,” advises us also to
not allow our ability to attend and to expend effort to dissipate through lack of regular
(daily) use:
[I]t is not simply particular lines of discharge, but also general forms of dis-
charge, that seem to be grooved out by habit in the brain. Just as, if we let
our emotions evaporate, they get into a way of evaporating; so there is reason
to suppose that if we often flinch from making an effort, before we know it
the effort-making capacity will be gone; and that, if we suffer the wandering
of our attention, presently it will wander all the time. Attention and effort
are […] but two names for the same psychic fact. To what brain-processes
they correspond we do not know. The strongest reason for believing that
they do depend on brain-processes at all, and are not pure acts of spirit, is
just this fact, that they seem in some degree subject to the law of habit, which
is a material law. As a final practical maxim, relative to these habits of the
will, we may, then, offer something like this: Keep the faculty of effort alive in
you by a little gratuitous exercise every day. That is, be systematically ascetic or
heroic in little unnecessary points, do every day or two something for no
other reason than that you would rather not do it, so that when the hour of
dire need draws nigh, it may find you not unnerved and untrained to stand
the test. (William James, 1890/1981, p. 126, italics in original)
The philosopher Gilbert Ryle (1958), in a paper titled, “On forgetting the difference
between right and wrong,” took the position that the phenomenal and experiential
content of ethics, or of that realm of knowledge that involves knowing “the difference
between right and wrong,” is so deeply interconnected with noncognitive aspects of
experience—with caring and with doing—that the notions of “forgetting” and “recol-
lection” simply do not apply. Ryle maintained that after a certain maturational point
has been reached in our ethical development, namely that point after which we can be
said to “know” the difference between right and wrong, these notions are irrelevant or
inapplicable.
Encountering this paper as a graduate student, studying human learning
and memory, I was decidedly unsettled by this assertion: It seemed to make values
something that were outside of (perhaps above) the “pale” of the usual vicissitudes of
representational accessibility, of forgetting, or failures to access ideals and standards,
and of the effects of recent encounters and exemplars of behaviors that one did, or did
not, wish to emulate. In contrast, my sense of the human mind, and of its capacities,
resonated much more closely with the view taken by William James, in his Principles
Impl ications and Appl icat ion s of iC ASA 611
ideals and values are therefore vulnerable to remarkable failures, including failures
of not always coming (or remaining) in the fore of consciousness to guide our actions
and judgments when needed. Equally important, however, they are therefore
also open to the remarkable potential for reemergence—and strengthening and
heightened accessibility—that may be engendered by our own choices and acts, and by
the environments that we choose and make for ourselves and for each other.
Notes
Chapter 1
1. For some of the possible reasons for the predominant alignment of emotional processing
with System 1 and the experiential system, see, for example, Loewenstein et al. (2001) on
“risk as feelings.”
2. Hodgkinson et al. (2008) remark particularly on the point that, given that intuition and
rationality in the cognitive-experiential self theory proposed by Epstein and colleagues may
be separate dimensions (rather than ends of a single continuum), this theory ascribes “greater
agency to individuals, arguing that analytic and intuitive processing capabilities are served
by cognitive systems that permit individuals to switch back and forth strategically from one
approach to the other, as required, albeit moderated to some extent by stylistic preferences”
(Hodgkinson et al., 2008, p. 8, emphasis added).
3. Note that recognition-primed decision making in this sense, of skilled pattern-based or
exemplar-based judgments, should not be confused with the “recognition heuristic” charac-
terized by Gigerenzer and colleagues (e.g., Goldstein & Gigerenzer, 2002; cf. Oppenheimer,
2003), where one’s ability to either recognize a stimulus, or not, is taken as a simplifying
“stand in” for another attribute that one does not know. In this latter case, recognition is used
as a simplifying heuristic, as a rule of thumb involving “attribute substitution” (e.g.,
Kahneman, 2003). For further discussion of heuristics, see note 10 for this chapter.
4. Similarly, Osbeck (1999, p. 231) remarks that, within experimental psychology, “Intuition is
frequently assumed to be the basis for judgments made rapidly and easily, without aware-
ness of the inferences supporting them. [. . .] Typically, performance based on ‘intuitive’
judgments of the correct solution to a problem [is] compared with some established,
‘scientific’ procedure for arriving at a solution. Much of the research of this nature, particu-
larly in earlier studies, focuses on the shortcomings of intuition in comparison with rational
processing.” Osbeck (1999) reviews and contrasts multiple interpretations of intuition in
psychology and philosophy, and ultimately concludes that narrowly construing it only in
terms of providing unconscious inferential grounds for judgments and decisions is to over-
look its central role throughout cognition. It involves a significant failure to recognize other
psychological phenomena that are also notably close to the principal philosophical mean-
ings of this notion, such as that of “direct perception” in J. J. Gibson’s (1979) ecological
theory, Gestalt notions of the priority of relationship/form (e.g., Kohler, 1925), and the
relations between intuition and implicit learning (A. S. Reber, 1989, 1993) and ideas of tacit
knowledge (Polyani, 1967). She argues that “a developed theory of intuition would be an
integrative one, incorporating indications of direct, noninferential apprehension within
theories of perception, development, emotion, and language use, making links, where
appropriate, with evidence from neuroscience” (Osbeck, 1999, p. 246). As an example of the
613
614 N O T E S T O PA G E S 22–29
such links, Osbeck (1999) points to neuropsychological evidence, using the Iowa Gambling
Task, provided by Bechara et al. (1997, p. 1294), that “covert biases . . . facilitate the efficient
processing of knowledge and logic necessary for conscious decisions,” as “suggesting their
foundational relationship to logic and conscious thought” (Osbeck, 1999, p. 246). Although
the relative roles of cognitive and emotional/somatic processing in the Iowa Gambling Task
continue to be debated (e.g., see Guillaume et al., 2009, for review), and the task may
specifically pose a problem of reversal learning (Fellows & Farah, 2005, discussed in Chapter
8), the incorporation of neuroscience findings into the study of intuition (see Chapter 9)
and of decision making more broadly (e.g., R. Yu, Mobbs, Seymour, & Calder, 2010) has
greatly accelerated since the time of Osbeck’s review.
5. The concept of “cognitive flexibility” might also clearly be considered here—and is explicitly
treated later in this section particularly in connection with the concept of creativity. Here,
however, it might be noted that the range of application of this term in the cognitive and
cognitive neuroscience literatures has also frequently been quite specific, and centered on the
deliberate/controlled side of the levels of control continuum. “Cognitive flexibility” has been espe-
cially used to denote an aspect of executive function pertaining to an individual’s capacity to
notice and appropriately respond to changing contingencies or rules, such as “switching” the
rule used to guide responding during a task that requires attention to different dimensions
of a stimulus (e.g., in the Wisconsin Card Sorting Task), and where the changing contingen-
cies are themselves often “unannounced.” This term has not typically denoted changes
between more deliberate/controlled processing and more spontaneous or habitual respond-
ing, and it generally refers to attention-demanding controlled shifts in responding, involving
subprocesses or submechanisms such as set shifting, updating, and maintenance of set.
Other more specific constructs related to cognitive flexibility, and referring to particular
aspects of behavior in laboratory-based paradigms such as card sorting and other tasks,
include the following: intradimensional vs. extradimensional set shifts, where the attentional
shifts are made, respectively, within an already relevant stimulus dimension versus to a
newly relevant stimulus dimension; reversal learning, denoting the capacity to learn that a
stimulus-reinforcement association has been reversed and characterized as entailing a form
of affective shifting; and task switching, usually but not always involving the requirement to
switch between particular tasks and task goals in response to externally provided signals.
Distinctions between these more focused constructs are taken up in Chapter 8, in the
section titled, “Neurochemical and Neuroanatomical Contributions to Three Forms of
Cognitive Flexibility: Set Shifting, Reversal Learning, and Task Switching.”
The further concept of spontaneous flexibility—denoting internally prompted changes in
especially strategic versus automatic responding, and typically viewed as especially influen-
tial in tasks designed to tap both fluency and originality of responding such as divergent
thinking tasks—is also considered in Chapter 8, as well as at multiple additional points
(e.g., see the discussion of the benefits of performing the Alternative Uses Task on subse-
quent insight problem-solving performance in the third section of Chapter 2; see also the
section on “adaptive flexibility” in relation to the personality dimension of openness to
experience in Chapter 6, and “Brain Correlates of Insight Problem Solving” in Chapter 9).
6. Martindale (1999, pp. 148–149) concluded a review of the biological bases of creativity with
the statement that “All of the theories of creativity reviewed say essentially the same
thing—that creative inspiration occurs in a mental state where attention is defocused,
thought is associative, and a large number of mental representations are simultaneously
activated. Such a state can arise in three ways: low levels of cortical activation, compara-
tively more right- than left-hemisphere activation, and low levels of frontal-lobe activation.”
However, intriguingly, and more in line with the iCASA framework suggested here, unlike
these proposals, Martindale proposes that, rather than being a stable trait of creative
people, defocused attention is a variable state, such that “creative people are better at adjust-
ing their focus of attention depending on task demands [. . .] and that this adjustment is auto-
matic and reactive rather than one involving self-control. In essence, creative people exhibit
Not e s t o pag e s 2 9 – 4 0 615
differential rather than reduced focusing of attention. In earlier phases of problem solving when
the problem is relatively ill defined, creative people are more likely to defocus attention.
This tendency makes the central task more susceptible to interference by seemingly
irrelevant information, some of which may provide the building blocks for solutions.
However, this widening of attention comes at the cost of slowing down processing on the
task. In later stages of problem solving when creative people are verifying developed ideas,
performance will benefit through the inhibition of irrelevant stimuli and added focus on the
task. This narrowing of attention speeds up processing on the task” (Vartanian, Martindale,
& Kwiatkowski, 2007, p. 1471, emphasis added; also see L. Dorfman, Martindale,
Gassimova, & Vartanian, 2008).
7. For example, based on a recent extensive analysis of the interrelations between a large
number of different measures, Salthouse and colleagues (2008) concluded: “Although
motivated from different research traditions and usually studied separately, the results of
this and other recent studies suggest that research with cognitive, psychometric, and
neuropsychological variables may have been characterizing essentially the same dimension of
individual differences among normal healthy adults. Whether this dimension is labeled
Gf [fluid intelligence], working memory, executive processing, or some form of cognitive
control may reflect the research tradition of the investigator more than any fundamental
differences among the concepts because it appears that individuals would be ordered in
nearly the same way with variables from each of these perspectives” (Salthouse, Pink, &
Tucker-Drob, 2008, p. 483, emphasis added; for additional discussion, see Ackerman, Beier,
& Boyle, 2005, and Kane, Hambrick, & Conway, 2005).
8. Research conducted within this approach has also provided recent and intriguing
evidence of detrimental effects arising from “too much” control. Under some circumstances,
requiring additional processing during a task may actually enhance performance because it
“forces” the individual to rely to a greater extent on parallel processing mechanisms.
Participants “forced” to forego step-by-step processing appeared to avoid a processing
bottleneck in which new perceptual information that is rapidly repeated may be missed
(i.e., “repetition blindness,” see Taatgen et al., 2009).
9. Parallel encoding of representations at different levels of representational specificity need
not exclude a possible role for the effects of repeated retrieval or reactivation of a memory in
the extraction of a schematic or gist-based representation of events from autobiographical
memories, as in the Multiple Trace Theory proposed by Moscovitch et al. (2005). According
to this account, each reactivation of a memory trace (recollection or remembering) leads to a
reencoding of the information by the hippocampus/medial temporal lobe system, resulting
in “multiple traces” of the event or place, some of which may be highly detailed and episodic,
but others that may be more schematic or gist-like. As succinctly summarized by Moscovitch
(2009, p. 68), “With respect to semantic memory, reactivation of memory traces accom-
plishes two things: Because each reactivated trace shares some neocortical representations
with previous traces, reactivation slowly instructs the development of neocortical traces that
reflect the statistical properties of the world and/or of memories—the gist or semantic core
is extracted [. . .]. Reactivation of memory also facilitates formation of links between repre-
sentations of elements of episodes.” See also Rosenbaum et al. (2009).
10. A highly salient comparison here concerns the use of heuristics, such as the “recognition heu-
ristic,” which are “fast and frugal” routes to reaching a decision (e.g., Gigerenzer & Goldstein,
1996) because—broadly stated—they ignore part of the information and consider only one
or a few aspects (e.g., whether one recognizes one of the alternatives). There has been a tre-
mendous resurgence of research on the use of heuristics, related to the question of the use of
“simple heuristics that make us smart” (see Todd & Gigerenzer, 2000, for précis). Shah and
Oppenheimer (2008) suggest that all heuristics act to reduce one or more of the effortful
steps involved in applying the “weighted additive rule” and its variants in reaching a decision.
The weighted additive rule is a complex algorithm for arriving at optimal decisions and
accurate judgments (Payne, Bettman, & Johnson, 1992). To apply the weighted additive
616 N O T E S T O PA G E S 40–58
rule, the decision maker must consider all of the available alternatives and cues for each
alternative; weight each cue according to his or her subjective or objective impressions as to
how much it contributes to an alternative’s overall value; and then calculate the value of
each alternative by multiplying each cue by its corresponding weight and summing all of
these values to obtain the overall value for an alternative. Shah and Oppenheimer outline
five possible methods for “effort-reduction” in applying this algorithm, including examining
fewer cues, reducing the difficulty associated with retrieving and storing cue values, simpli-
fying the weighting principles for cues, integrating less information, and examining fewer
alternatives.
Notably, Gigerenzer has explicitly contested several common misconceptions regarding
heuristics, such as that more information and computation is always better, arguing that
“good decisions in a partly uncertain world require ignoring part of the available informa-
tion” so as, for example, to foster robustness. Shah and Oppenheimer (2008, p. 220)
similarly explicitly remark that “heuristics may sometimes appear as optimal or suboptimal,
expected or surprising, but they should foremost share the common goal of reducing the
effort associated with a task.”
See Gigerenzer (2008), “Why heuristics work;” Shah and Oppenheimer (2008), “Heuristics
made easy: An effort-reduction framework;” and Weber and Johnson (2009), “Mindful
judgment and decision making” for integrative review and discussion. The “fluency
heuristic” is discussed in Chapter 4 in the subsection on “The Perils of Repetition, Rhyming
Truths, and Such: The Overreaching Effects of Fluent Processing.”
11. See Solomons & Stein (1896), and Stein (1898). For a historical consideration of the work of
Gertrude Stein and Leon Solomons, see Koutstaal (1992).
Chapter 2
1. Some children with autism who demonstrate superior memory in a particular domain may
show a similar retention of the physical aspects of language. Wilding and Valentine point to
the case of Elly, who had “virtually perfect memory for any route she had travelled” and
“could often repeat large parts of conversations she had heard about topics that were unfa-
miliar to her”—but could not understand metaphor. She was “obsessed with discovering
regular physical patterns in the world, in language and especially in numbers” (1997, p. 49).
2. The memory and categorization performance of patients with semantic dementia (Hodges
et al., 1992; Hodges & Patterson, 2007) provides a very different example of the potential
costs of a near-exclusive reliance on specific perceptual and episodic memory. Semantic
dementia is a form of progressive brain disorder (the “temporal variant” of frontal-temporal
dementia) that, in its early stages, involves largely circumscribed atrophy of the anterior
temporal lobes. Unlike in Alzheimer’s disease, memory for recent events (episodic memory)
is mostly spared during the early course of semantic dementia. However, the disease leads to
a progressive loss of semantic memory or knowledge of concepts, such as what a lamp is, or
what an elephant is, their important and defining characteristics, what they are called, and
so on. This loss of conceptual knowledge impedes the individual’s ability to extrapolate
relevant knowledge from one member of a category to other instances of the same general
sort. Although these patients often show isolated islands of preserved knowledge of the
functions of the particular common objects that they use everyday (e.g., their own hairbrush
or scissors), and for other objects that are very perceptually similar to those objects, they
cannot draw upon more abstract knowledge of objects and so may have no idea how to use,
for example, an unfamiliar set of scissors (Bozeat et al., 2002; Hodges et al., 1992; Ikeda
et al., 2006; Snowden et al., 1996; also see Graham et al., 2000). The first section of Chapter
9 details several important insights into how concepts are represented in the brain that have
been derived from considering the semantic cognition of persons with semantic dementia.
3. Simner et al. (2009, p. 1249) underscore five characteristics of AJ’s “mental calendar” that
suggest it reflects a form of synaesthesia for time and space. They note that her mental
Not e s t o pag e s 5 8 – 6 7 617
calendar: “appears in specific mental arrays, which date back as long as she can remember,
whose roots are unknown to her, but which are highly consistent over time, and which
conform to known shapes common among other time-space synaesthetes.” According to
this suggestion, AJ’s “obsessive tendencies [may] give her not only an obsession with the
past (the first trait of hyperthymestic syndrome), but [may] have also allowed the superior
recall normally associated with time-space synaesthesia to become heightened and refined
over time, into a savant-like ability (the second trait of hyperthymestic syndrome).
A related, but more conservative proposal might simply be that synaesthetic mental calen-
dars increase the likelihood of hyperthymestic syndrome” (Simner et al., 2009, p. 1256).
4. There are several discrete circuits between the dorsal and ventral striatum and prefrontal
cortical regions, including circuits that have been designated as motor, oculomotor, dorso-
lateral, ventral/orbital, and anterior cingulate circuits (G. E. Alexander et al., 1986). In an
extensive review of the cognitive functions of the caudate nucleus, Grahn, Parkinson, and
Owen (2008, p. 141) concluded that “the caudate nucleus contributes to behaviour through
the excitation of correct action schemas and the selection of appropriate sub-goals based on
an evaluation of action-outcomes; both processes [are] fundamental to successful goal-
directed action.” In contrast, they concluded that the putamen “appears to subserve cogni-
tive functions more limited to stimulus-response, or habit, learning” and that “this modular
conception of the striatum is consistent with hierarchical models of cortico-striatal func-
tion through which adaptive behaviour towards significant goals can be identified (motiva-
tion; ventral striatum), planned (cognition; caudate) and implemented (sensorimotor
coordination; putamen) effectively.”
5. There is another type of general memory that involves an extended time period, such as
“our first trip to Rome,” that, like categorical memories, also refer to events that did not
occur on a single day. The frequency with which depressed or parasuicidal individuals
provide instances of such “extended memories” does not reliably differ from the frequency
with which nondepressed people generate such memories (e.g., J. M. G. Williams &
Dritschel, 1988). This suggests that it is the processes of event categorization, and of access-
ing particular individuated events within an event category, that are particularly important in
the phenomenon of overgeneral memory in depression. This suggestion is in line with the
models of memory access proposed by researchers such as M. A. Conway and Pleydell-
Pearce, and J. M. G. Williams and colleagues, considered later in this section.
6. Specifically, in line with each of the R. M. Baron and Kenny (1986) criteria, separate regres-
sion analyses demonstrated that (a) the experimental condition (1 = concrete, 0 = abstract
self-focus) was a significant positive predictor of change in problem solving, (b) the experi-
mental condition was a significant positive predictor of change in concreteness of problem
descriptions, (c) changes in concreteness were significantly associated with changes in
problem solving, (d) this association between concreteness and change in problem solving
remained significant even when experimental condition was also included in the regression
equation, and, contrariwise (e) when change in concreteness was entered into the regres-
sion equation, experimental condition was no longer a significant predictor of change in
problem solving.
7. There is also some evidence that rumination is itself associated with cognitive inflexibility,
even in healthy young individuals (Davis & Nolen-Hoeksema, 2000). Compared with indi-
viduals who reported no or very few ruminative tendencies, individuals who reported that
they often engaged in ruminative patterns during depressed mood states, including self-
focused responding (e.g., “I think, ‘Why do I react this way?’”), symptom-focused thoughts
(e.g., “I think about how hard it is to concentrate”), and a focus on the possible causes and
consequences of their mood (e.g., “I think, ‘I won’t be able to do my job if I don’t snap out of
this’”), showed more frequent perseverative errors on the Wisconsin Card Sorting Task.
They also more frequently failed to maintain cognitive set even after successfully switching
to a new category sorting rule, suggesting that they may have difficulty adapting and main-
taining their cognitive set in accordance with changing environmental contingencies.
618 N O T E S T O PA G E S 68–79
and knowledge are inextricably situated in their social and material contexts (e.g.,
J. S. Brown, Collins, & Duguid, 1989; R. Hall, 1996). However, it is argued that transfer
requires additional mechanisms to allow cross-situational transfer. Given the association of
abstraction with decontextualization—as in the quotation from L. S. Fuchs et al. (2003)
later in this section—R. A. Engle (2006) opted instead to use the term “generalization,”
concurring with many situative theorists that “there is no reason that generalizations
cannot be deeply tied to the contexts in which they arise” (R. A. Engle, 2006, p. 454).
14. Although this study involved direct reminding probes in which participants were asked to
read stories and then write down as accurately as possible any of the stories rated earlier of
which they were reminded, a further experiment, requiring participants to write all stories
they were reminded of showed similar outcomes for the first retrieved remindings. These
convergent outcomes suggest that the remote-analogy over remote-disanalogy advantage
did not simply reflect “postretrieval editing” of stories (where participants only reported
the remote analogy stories they perceived as relevant, even though they also retrieved
remote disanalog stories).
15. This strategy also is particularly likely to be relied upon in situations where the decision
maker is under time pressure, and where there is uncertainty and/or ill-defined goals.
It is less likely to be adopted in other circumstances, such as where the views of multiple
stakeholders need to be taken into consideration, or justifications are required (Lipshitz
et al., 2001).
Chapter 3
1. In a detailed conceptual analysis of mindfulness, S. L. Shapiro and colleagues (2006)
argued that it involves three components: (i) intention, corresponding to the notion of
“on purpose,” or why one is practicing mindfulness, and which may change over time; for
example, from an initial aim of self-regulation, to that of self-exploration, and then to that
of self-liberation; (ii) attention, including several subcomponent skills, particularly the
ability to attend for long periods of time to a particular object or task (vigilance or sustained
attention; e.g., Parasuraman, 1998; Posner & Rothbart, 1992), the ability to shift the focus of
one’s attention between objects or mental sets (switching; Posner, 1980), and the ability to
selectively and appropriately inhibit thoughts, feelings, and sensations (cognitive inhibition;
J. M. G. Williams, Mathews, & MacLeod, 1996); and (iii) attitude or mindfulness qualities, in
which, by “intentionally bringing the attitudes of patience, compassion and non-striving to
the attentional practice, one develops the capacity not to continually strive for pleasant
experiences, or to push aversive experiences away” (S. L. Shapiro et al., 2006, p. 377).
2. For a consideration of how mindfulness meditation differs from the cognitive model of
mindfulness forwarded by E. Langer and colleagues (e.g., Langer, Blank, & Chanowitz, 1978;
Langer & Moldoveanu, 2000; Langer & Piper, 1987), see Baer (2003) and Sternberg (2000).
Although the approaches share an emphasis on flexible awareness in the present, Langer
and Moldoveanu (2000, pp. 1–2) suggest that the latter can be best characterized as
“the process of drawing novel distinctions”—a process that then has several further effects,
such as helping to keep us “situated in the present” and “more aware of the context and
perspective of our actions than if we rely upon distinctions and categories drawn in the
past.” Such reliance on past distinctions and categories is held to make it more likely that
our behavior will be governed by rules and routines without regard to the current circum-
stances, and “this can be construed as mindless behavior.”
Mindfulness interventions based on this model often include a focus on external materials,
and active, goal-oriented cognitive tasks, such as solving problems. It is proposed that
there are diverse (beneficial) consequences from drawing novel distinctions, including:
“(1) a greater sensitivity to one’s environment, (2) more openness to new information,
(3) the creation of new categories for structuring perception, and (4) enhanced awareness
of multiple perspectives in problem solving” (Langer & Moldoveanu, 2000, p. 2). These
620 N O T E S T O PA G E S 92–103
authors further observe that the predominant feeling, subjectively, of mindfulness is that
of “a heightened state of involvement and wakefulness or being in the present” and that
“mindfulness is not a cold cognitive process. When one is actively drawing novel distinc-
tions, the whole individual is involved.” It is thus clear that mindfulness in this sense and
“agility of mind” are also conceptually related. However, like the concepts such as “executive
control” or “executive attention,” discussed in Chapter 1 in the section on “Distinguishing
Agile Thinking,” mindfulness too selectively and too exclusively emphasizes the relatively
more “controlled” portions of the automatic-spontaneous-controlled continuum, under-
weighting the substantial contributions of less controlled and more automatic processing to
creatively adaptive thinking and problem solving.
3. Although the Stroop task is often thought of as a paradigmatic example of highly automatic
responding, other research similarly demonstrates that the extent to which we are likely to
be “automatically captured” by the highly habitual tendency to read text or other meaning-
ful symbols can be modulated by task and attentional factors. Besner (2001, p. 324), for
example, has suggested that although the more common (default) set may be to process
words to the highest (semantic) level, “these reading processes are (contextually) controlled
rather than ballistic.” Other investigators have reported that performance on the Stroop
task may be modified by suggestion, such as the posthypnotic suggestion that the words
will appear as meaningless symbols that feel like characters of a foreign language that one
does not know (Raz, Fan, & Posner, 2005; Raz, Kirsch, Pollard, & Nitkin-Kaner, 2006),
leading to the conclusion that “cognitive processes that have been automatized through
practice can be de-automatized and brought under cognitive control” (Raz et al., 2006, p.
94). In Chapter 5, we also consider evidence that forming a specific implementation inten-
tion, to the effect that “as soon as a word appears, I will ignore its meaning” similarly may
help to circumvent such interference effects.
4. One possible alternative account of these findings might be that there is simply an advan-
tage to performing the same sort of recognition decision throughout the testing situation
(as in the III condition) than if individuals need to change the level of specificity with which
they make their recognition decisions part way through the testing (as in the CCI condi-
tion). However, additional comparisons, with further experimental conditions (Koutstaal &
Cavendish, 2006), argue that these effects do not simply reflect an advantage in the III
group from performing the same task across all three tests. Unlike what would be expected
from this same task account, there is no corresponding benefit for category-based recogni-
tion if individuals are asked to consistently retrieve information in a category-based manner
(CCC group) versus initially retrieving item-specific information and then switching to cate-
gory-based retrieval (IIC group). For these latter conditions, there was no advantage for the
CCC group relative to the IIC group on any measure and, if anything, numerical differences
in sensitivity favored the group that initially engaged in item-specific retrieval.
5. The claim that individuals generally prefer higher level, more abstract construals of their
activities and actions rather than lower ones echoes one of the points made in Chapter 2 in
connection with failures to transfer knowledge to new situations or problems. There, it was
asked whether it is really the case that individuals have a general propensity toward noticing
and retrieving superficial, surface details of situations and the stimuli that they encounter. It
was argued that experimental findings in the analogical problem-solving and learning litera-
tures pointing to “surface superiority” or the “primacy of the mundane” are moderated by
many factors, including expertise. With regard to the interpretation of our own actions and
those of others, most individuals might generally be thought to be at least moderately profi-
cient if not quite “expert,” even if also prone to error and bias in some contexts, and so might
mainly adopt a relatively higher level of action identity with regard to many everyday actions.
6. Note that these stated contrasts seem to suggest that higher level construals are not only
more abstract but also more “valuable” in some normative sense. I have quoted here
the terms and descriptors used in Fujita et al. (2006); it is not my own view that lower
level construals are necessarily of less value—clearly it will depend; furthermore, what is
Note s t o pag e s 1 0 3 – 1 3 5 621
“incidental” depends on a given set of purposes or constraints, and what is “unique and
specific” may, again, depending on circumstances, be valued precisely for those very
characteristics.
7. For instance: Might a dimly lit, cluttered, and difficult-to-navigate space lead to a more
“low-level” construal of what one is doing and the choices one is making (e.g., in an old
factory warehouse) than if one were in a large, spacious, and luxurious space that seems to
make all of one’s movements gracefully effortless (e.g., in the entry lobby of a five-star
hotel)? Some recent findings suggest that these questions may not be quite as far-fetched as
they, at first, seem. For example, when individuals are aware of height, high ceilings may
activate abstract relational thinking, whereas low ceilings more strongly activate concrete,
item-specific processing (Meyers-Levy & Zhu, 2007). Clearly this does not mean that high
ceilings are necessarily best; it will depend on the tasks and purposes at hand, but it does
strongly suggest that we are “situated beings,” shaped and primed by our environment in
many ways, not all of them obvious, or readily fully charted.
8. Schunn and Dunbar even suggest that, “Given the constructive nature of human memory
[. . .] it is highly likely that many of the reports of the origins of specific hypotheses in
science are incorrect. The scientists may not have a memory of where their hypotheses
came from because their hypotheses were the result of priming, and they must construct a
non-veridical story that gives the origin of their hypotheses” (1996, p. 282).
Chapter 4
1. Research such as that by Barsalou and Wiemer-Hastings (2005) persuasively argues
that even abstract concepts, such as “truth,” “freedom,” and “invention,” are grounded in
complex perceptual simulations involving combined physical and introspective events
(e.g., affect/emotion and evaluation). However, these and related findings, such as those of
J. M. Mandler (2004a, 2004b), Gibbs (2006), and Boroditsky (2000; Boroditsky & Ramscar,
2002) showing an important role of image-schemas and of spatially grounded metaphor in
understanding many abstract notions such as “containment” or “time,” do not support the
much stronger claim that all conceptual thinking necessarily or exclusively depends on a
grounding in the perceptual senses. As Goldstone et al. (2005) argue, even highly concrete
concepts, such as “horse” are associated with many further concepts that are less concrete
than “horse” itself, such as “freedom,” “domesticated,” and “strength.” Neither such inter-
conceptual relations, nor the more concrete, experientially derived relations that are
anchored in perception and action, need be forfeited: “Sensory reduction can be avoided by
positing interconceptual relations such as these, that coexist with perceptual groundings.
We do not have to choose between meaning based on interconceptual relations or percep-
tual senses, and by not choosing we make it much more plausible that all of our concepts
have perceptual-motor components. Moreover, it is not simply that these complementary
aspects of meaning coexist. Internal and external bases of meaning are mutually reinforcing,
not mutually exclusive” (Goldstone, Feng, & Rogosky, 2005, pp. 310–311, emphasis added).
2. There are differing versions of the candle problem, and Duncker (1945, p. 86) actually
referred to this as the “box problem.” In Duncker’s version, there were three larger candles,
and three small pasteboard boxes, that were either filled with, respectively, several thin little
candles, tacks, and matches, or were unfilled. In his version, the solution was to use the
tacks to mount the boxes to the door. The problem in the text is a simplified version.
3. Although here we are focusing on the effects of perceptual simulation in relation to objects,
it is important to note that the particular movements associated with actions may also be
covertly reinstantiated during language comprehension. Listeners or readers with greater
experience in a given domain (e.g., ice hockey) showed larger “action-match” effects: that is,
greater facilitation for pictured individuals whose actions matched those implied in the sen-
tence relative to pictured individuals whose actions did not match those implied by the sen-
tence (Holt & Beilock, 2006). Participants also showed greater activation in left dorsal
622 N O T E S T O PA G E S 135–156
elliptic and indexical” and diverges considerably from written language; second, laboratory
talk is accompanied by a large number of gestures that help to disambiguate students’ ellipti-
cal speech, particularly gestures that “point to, or stand in iconic relation to, the representa-
tions and phenomena at hand,” and third, the precision and clarity of laboratory talk evolves
over time, gradually becoming more scientifically appropriate. Both deictic and iconic
gestures would sometimes considerably precede an individual’s verbal mastery of a concept,
so that “gestures appear to scaffold the emergence of students’ observational and theoretical
language about the phenomena they study” (W. M. Roth & Lawless, 2002, p. 287).
10. Further research shows that, even without a “conversational intention” the motor actions
that we perform, including such simple actions as pressing versus pulling a lever, or nodding
versus shaking our head, may have intersections with thought. How we ourselves physically
respond to words or objects, that is, the particular motor actions that we use in expressing
an evaluative judgment about the object, may not be entirely neutral or inconsequential
activities, but may be either congruent with the decision (e.g., pushing away from the self
when making an evaluative judgment about an undesired or to-be-avoided object, or pulling
toward the self when making an evaluative decision about a desired object) or incongruent
(pushing away desired objects; pulling undesired objects inward). Cacioppo et al. (1993)
showed that novel stimuli (ideographs) that were first presented during arm flexion were
rated more positively than were ideographs first presented during arm extension. M. Chen
and Bargh (1999) showed that individuals responded more quickly to words shown on the
computer screen when they were asked to perform a pulling movement, and the word was
positive in valence (approach), or to perform a pushing movement, and the word was nega-
tive in valence (avoid), than if there was a mismatch or movement incompatibility.
Using an ingenious manipulation of an individual’s representation of herself in space relative
to associated objects—by projecting the person’s first name into a “virtual corridor” such
that the name appeared in the middle of the corridor and then placing positive and negative
words either in front of, or behind, the individual’s name—Markman and Brendl (2005)
demonstrated that the movement compatibility effect concerned not the individual’s body
(where she was in physical space) but her name. That is, the compatibility effect was still
observed in this projected world experiment, but the compatibility effect was in relation to
the location of the name (the projected self, involving pushing vs. pulling negatively or posi-
tively valenced objects towards the person’s own name) rather than the actual physical
movements in relation to the body (pushing vs. pulling toward the body).
Additional recent research (van Dantzig, Zeelenberg, & Pecher, 2009) has shown that simi-
lar movement compatibility effects can be obtained with virtually projected words and
stimuli other than one’s name (e.g., a category name, or even just a box on the screen), argu-
ing that the movement compatibility effect involves flexible complex representations of
one’s task goals, rather than an automatic fixed association to where one is (literally) in phys-
ical space. As van Dantzig and colleagues (2009, p. 350) observed, “The idea that cognition
is grounded in the systems of perception and action does not necessarily imply that cogni-
tive concepts are mapped directly onto very low-level sensorimotor representations. It is
more likely that concepts are linked to the perceptual and motor system at a higher level of
representation (e.g., the level of the action goal). Such higher-level representations obvi-
ously are more abstract than the low-level representations, but they are still firmly grounded
in perception and action.”
11. The intimate connectedness of the ways in which words are physically realized externally in
the outside world and the process of writing is poignantly underscored by the case of the
playwright Eugene O’Neill who, after developing Parkinson’s disease, was unable to make
the transition from handwriting his works to dictating them. Sharon Cameron speculates
that the difficulty experienced by O’Neill, compared with the relative ease experienced
by Henry James in the transition to dictating his novels, might originate in the differing
conceptions that the two writers had of consciousness itself. Cameron writes, “For O’Neill,
who stopped being able to write his plays when he stopped being able to write them down,
624 N O T E S T O PA G E S 166–192
consciousness flows from the brain, through the arm, into the pencil, and onto the paper,
where it ends. For the Henry James of the novels, as for his characters, that is where it
starts: at the limits of the self, it is ultimately defined by its sweep or its range. Outside and
between persons, therefore undemarcated, consciousness may be said to be or begin”
(Cameron, 1989, p. 82).
12. The text of the following two sections is a modified excerpt from a longer paper exploring
the many roles of the physical nature of words in cognition: Koutstaal (2001), The edges of
words. Semiotica, 137, 57–97. Excerpted text is reprinted here with permission from De
Gruyter Mouton. For the earlier paper, see http://www.reference-global.com/doi/
pdf/10.1515/semi.2001.108.
13. The so-called mere exposure effect involves an increase in individuals’ ratings of how much
they like a stimulus (particularly unfamiliar novel objects) as a result of prior exposure to
the stimulus (repeated objects), relative to a stimulus that has not been previously exposed
(new objects). Although the mere exposure effect has been assumed to be a subtype of
“repetition priming” (e.g., Seamon et al., 1997), some characteristics clearly differentiate it
from standard forms of perceptual priming. For instance, whereas both mere exposure and
repetition priming effects are found for nonword stimuli, real words may produce repetition
priming but not mere exposure (L. T. Butler, Berry, & Helman, 2004; see L. T. Butler &
Berry, 2004, for review). The mere exposure effect also recruits brain regions that are
involved in emotional processing (e.g., amygdala, medial prefrontal cortex, and posterior
cingulate) and that are not necessarily recruited during a standard perceptual “repetition
priming” procedure such as perceptual identification (Koutstaal, Butler, Coates, & Simons,
unpublished data).
Chapter 5
1. Given that many of the higher level goals endorsed by the obsessive-compulsive patients
and the clients at the alcohol treatment center related to achieving a particular internal
emotional or cognitive state, it might be suggested that it was, in part, this focus on internal
states that was the “true” source of the difficulty with the higher-level identifications. Yet,
this, in turn, raises the question of the ultimate source of “evidence” that any of our higher
level goals have been achieved. For instance, how does an artist know (or decide) that a
given work of art is done, versus still in need of “one more move”? What is the “signal” that
it is, or is not, complete?
2. This particular example also might be seen as involving the formation of an “implementa-
tion intention,” because it takes the form of “when I encounter situation x, I will do y” (e.g.,
Gollwitzer & Brandstätter, 1997). As developed in the next section, on remembering inten-
tions and control, implementation intentions may boost the likelihood of successful inten-
tion fulfillment both as a result of their high level of specificity and because they recruit
more associatively and automatically based processes that help us to remember at the
opportune time and place without the need for extensive conscious monitoring.
3. There is an ongoing debate concerning the relative advantages and disadvantages of an
approach based on personality types versus dimensions to the study of personality, although
also some emerging consensus that both may prove beneficial under some circumstances, or
for different purposes (e.g., Asendorpf, 2003; Asendorpf & Denissen, 2006; Costa et al.,
2002). The aim here is to characterize contributors to agile thinking, and findings relating to
ego resilience and ego over-/undercontrol, obtained using the typological Q-sort technique,
are highly relevant to this aim. However, personality dimensions are likewise extremely
important and informative with regard to agile thinking—for instance, the dimension of
openness to experience, as particularly developed in the section on “Openness to Experience,
Creativity, and Adaptability” in Chapter 6. Arriving at a clearer understanding of the rela-
tions between these constructs and related biological and environmental underpinnings
and modulators (e.g., Eisenberg, Fabes, Guthrie, & Reiser, 2000; Hart, Eisenberg, & Valiente,
2007) is crucial in developing a fuller understanding of the agile mind.
Note s t o pag e s 1 9 4 – 2 2 0 625
4. Summarizing key ideas that also have been proposed by others, Martel et al. (2007, p. 544)
suggest that constructs such as resiliency and executive functions “are different levels of
analysis of the same basic psychological or even neural operations” and that “traits (or emo-
tion regulation) and executive functions (or cognitive control, here referring to strategic
but not reactive control) work together in an additive or interactive manner to shape action
selection, cognition, and behavior.”
5. Effortful control appears to be a relatively stable capacity. Using a comprehensive battery
of age-appropriate tasks involving effortful control in a variety of domains, and a variety
of response types (motor, vocal, or cognitive), within-child retest correlations on the
battery between ages of 2.5 and 5.5 years range between .58 and .69. Effortful control is
also multidimensional—composed of a number of different but related abilities, including
the abilities to delay, to slow fine or gross motor movements, and to suppress an ongoing
prepotent response and initiate an alternate response instead. Questionnaire data
indicate that (American) children high in effortful control tend to be low in negative
affect (Ahadi et al., 1993); a similar relation (high attentional control associated with low
negative affect) has been found in self-reports of adults (Evans & Rothbart, 1999; unpub-
lished manuscript cited in Rothbart, Ahadi, & Evans, 2000). Note that other investigators
have used different terms for the two forms of control, such as impulse and constraint
(Carver, 2005), reflective and impulsive processes (Strack & Deutsch, 2004), x-system and
c-system (Lieberman, 2007; Satpute & Lieberman, 2006), and good self-control and poor
self-control (e.g., T. A. Wills et al., 2006). See Dvorak and Simons (2009) for additional
discussion.
6. In his essay, “Vacations,” William James memorably defended the need for at least 2 weeks
of respite from the demands and routine of work each year, arguing that we need to protect
that “capacity for irresponsible enjoyment which is like air space in the character”
(1873/1987, p. 4) so that it does not become wholly atrophied within us. Chapter 12
discusses the question of both short-term and longer term ways of structuring our work
and learning lives to take appropriate heed of William James’s advice.
7. Other studies examining possible “real world” and also potential ethical implications of
self-regulatory depletion include evaluations of how academic examination stress impairs
self-control (Oaten & Cheng, 2005) and how prior self-regulatory challenges influence
sexual restraint (Gailliot & Baumeister, 2007) and aggressive responses with and without
provocation (DeWall, Baumeister, Stillman, & Gailliot, 2007). The effects of increased
self-regulatory demands during interracial interactions on interference control in a version
of the Stroop color-word task (Richeson & Trawalter, 2005) have also been shown. The self-
regulatory demands of stereotype suppression are considered later in this section with
regard to the work of Gailliot, Plant, Butz, and Baumeister (2007) on training interventions
to increase self-regulatory capacity.
8. Another biological measure that has been examined, using an outcome task of handgrip
strength following a cognitive depletion task (a modified Stroop color word task), is neuro-
muscular electromyographic (EMG) activity. Bray, Ginis, Hicks, and Woodgate (2008) found
that following depletion participants showed reduced handgrip endurance and also higher
forearm EMG activation, indicating greater muscle fatigue, on the postmanipulation
handgrip trial than did controls. Other work suggests that heart rate variability may be
another correlate of self-control, with individuals who show greater heart rate variability in
demanding self-control situations showing an increased level of self-regulatory strength
and effort (Segerstrom & Nes, 2007).
9. See also Higgins (2006), “Value from hedonic experience and engagement,” Psychological
Review, 113, 439–460.
10. In this section, we focus on the behavioral reinforcement of variable responding and of
originality. Nonetheless, many ways of eliciting variety can be imagined, including simply
the verbal imposition of explicit task constraints that require novel responses. Maltzman
(1960) suggests that Josiah Royce (1898), a philosopher and colleague of William James, may
have been the first to experimentally evaluate such verbal instruction as a straightforward
626 N O T E S T O PA G E S 220–230
Innovation at Corning was also about being willing and able to take failed
ideas and apply them elsewhere. As Weeks [the President and Chief Operating
Officer of the company] explained, “When an idea fails, we take that capabil-
ity set and say, ‘What else can we apply it to?’ From failure comes knowledge.
We aren’t usually successful with the first thing we try.”
(Henderson, R. M., & Reavis, C., 2009, Corning Incorporated: The growth
and strategy council. MIT Sloan Teaching Innovation Resources. https://
mitsloan.mit.edu/MSTIR/IndustryEvolution/CorningIncorporated/Pages/
default.aspx
Note s t o pag e s 2 3 1 – 2 7 0 627
15. As one of Wallace Stevens’ colleagues recollected, while Stevens was at work at his office at a
Hartford, Connecticut, insurance company: “He’d be writing them [lines of poetry] right
there at his desk, because he would stop dictating to [his secretary] Mrs. Baldwin. He would
stop right in the middle of dictating, and he would reach down in his right-hand drawer, and
he would just write down [something], put it back. I’ve seen him do that. He had a peculiar
filing system. He always filed his poetry notes in his lower right corner of his desk, which
was open most of the time to a degree. It seemed to me there were sheaves and sheaves. And
sometimes he would reach down, and he’d shuffle through three or four. He’d scratch out
something or put something in. Or he might take the top one and just add a line or two. All
of a sudden, he’d be reading a case, and I’ve seen him reach down in his drawer and just pick
something up. His private copies of his commercial work or his business letters would go in
his lower left-hand drawer.” P. Brazeau (1983), Parts of a world: Wallace Stevens remembered;
An oral biography. New York, Random House, p. 38.
16. Also see Charman and Howes (2003) on the circumstances under which computer users
develop more efficient approaches. These proposals are also in broad agreement with the argu-
ment that the development of conceptual and procedural knowledge involves bidirectional
causal relations between conceptual and procedural knowledge, and that these two forms of
knowledge often develop “in a gradual, hand-over-hand process” involving an iterative devel-
opment in both types of knowledge (Rittle-Johnson, Siegler, & Alibali, 2001, p. 358), each
often mediated by (and also producing) an improved representation of the problem.
Chapter 6
1. Notably, this study also provided some support for the converse pattern, with creativity also
fostering positive affect.
2. To date, most investigations of self-affirmation have involved the presentation of informa-
tion or messages that are relevant to the self, and often potentially threatening to the self.
Briñol et al. (2007) present preliminary findings that suggest that self-affirmation may
influence feelings of self-confidence, and thereby influence the degree of information
processing that is undertaken.
3. The term “Big Five” is generally restricted to measures derived from analysis of the
trait-descriptive lexicon, whereas factors derived from the questionnaire approach of
McCrae and Costa are termed the “Five Factor Model.” These approaches yield highly
correlated factors and the model is thus sometimes referred to as the Big Five/FFM
(e.g., D. E. Evans & Rothbart, 2007).
4. As noted, the precise term that should be used to designate the fifth factor is a matter of
considerable debate, and, perhaps in the effort to accommodate the divergent aspects
associated with the factor it is often designated with the combined terms “openness to
experience/intellect.” R. R. McCrae (1994) presents several sources of evidence suggesting
that the term “intellect,” although it may encompass many characteristics of the fifth factor,
is rather misleading. This is, in part, because certain aspects of intelligence (e.g., foresight,
analytical ability) also correlate strongly with the Big Five Conscientiousness factor. More
important, however, the term “intellect” may be misleading because it is overly narrow.
Many characteristics that contribute to the fifth factor of “Openness” do not necessarily
have a clear linkage to intelligence or intellectual ability per se, but are more psychologically
diverse than this term suggests. The six facets of Openness to Experience that are part of
the frequently used personality questionnaire, NEO-PI-R, and that are further character-
ized later in this section, namely Ideas, Fantasy, Aesthetics, Feelings, Actions, and Values,
clearly attest to considerable psychological diversity—diversity across multiple domains of
experience that is not well captured by the narrower term “intellect.”
5. Unlike most other aspects of personality, which do not consistently relate to measures
of intelligence, it has been shown that openness to experience is positively correlated
with general intelligence, with reported correlations on the order of .33 to .42 (e.g., Ashton,
628 N O T E S T O PA G E S 270–286
Lee, Vernon, & Jang, 2000; also see J. A. Harris, 2004). However, perhaps counter-
intuitively, the correlations between openness to experience and intelligence are higher for
“crystallized” intelligence than for “fluid” intelligence. For example, Ackerman and Goff
(1994) found a correlation of .32 between crystallized ability and Openness to Ideas,
whereas the correlation for fluid ability was only .13. Ashton et al. (2000) reported a similar
differential pattern when considering the overall fluid ability measure (correlation of .18)
compared to crystallized intelligence (.37). However, when considering particularly
pictorial aspects of fluid intelligence that involve pictures of objects, living things, or social
situations the correlation with openness was somewhat higher and significant (.24) than
when nonpictorial aspects were considered (arithmetic, spatial, and digital symbol, correla-
tion between nonpictorial fluid intelligence and openness of .08). A possible (but not
entirely satisfying) explanation for this pattern is that openness may relate more to a
broader approach to experience than to strictly “cognitive” measures and may not be fully
drawn out in the typical cognitive or neuropsychological testing situation during which fluid
intelligence is assessed.
6. Although here emphasizing the connections between reduced latent inhibition, creativity,
and openness to experience, it is important to note that there are also strong and well-
documented links between reduced latent inhibition and some forms of psychopathology,
particularly schizophrenia (e.g., Lubow & Gewirtz, 1995). The association of reduced latent
inhibition both with conditions involving maladaptive thinking and with highly creative and
innovative thinking requires an account of how attenuated preconscious attention gating
might apparently be associated with beneficial outcomes in one case, but harmful outcomes
in the other (e.g., G. F. Miller & Tal, 2007).
Multiple factors may be relevant here. One important factor may be the individual’s general
cognitive capacity for constructively grappling with the increased number and range of
sensory and cognitive stimuli to which reduced gating might leave the person exposed.
As suggested by Carson et al. (2003, p. 505), such a general cognitive capacity “may allow an
individual to override a ‘deficit’ in early selective attentional processing with a high-
functioning mechanism at a later, more controlled level of selective processing.” From this
perspective, “The highly creative individual may be privileged to access a greater inventory
of unfiltered stimuli during early processing, thereby increasing the odds of original recom-
binant ideation,” and “a deficit that is generally associated with pathology may well impart a
creative advantage in the presence of other cognitive strengths such as high IQ.”
7. Tolerance of ambiguity is one of five personality characteristics that Sternberg and Lubart
(1992) suggest is necessary for individuals who manifest sustained creativity.
8. Beyond focusing on situational or contextual factors that may differentially foreground the
positive features of openness to experience, it may also be important to consider subcompo-
nents of the openness to experience construct. For instance, B. Griffin and Hesketh (2004)
provide some suggestive preliminary evidence that predictions of job performance might be
improved through separately considering the three facets of openness to experience that
they propose mainly involve areas external to the person (Actions, Ideas, and Values) versus
those that are either internal to the person (Fantasy and Feelings) or essentially involve an
internal experience (Aesthetics), with only the former predicted to bear a relationship to job
performance. However, this approach, too, may require further modulation to accommo-
date differences in the nature of an individual’s occupational demands; for example,
high sensitivity to internal associative processes or feelings might be differentially more
important in contexts that require independent creative activity.
Chapter 7
1. See http://www.tomphillips.co.uk/portrait/sbec/
2. The beads task also has been used in individuals who have developed delusions. Similar to
anxious individuals, persons with delusions may “jump to conclusions” even for these very
neutral stimuli (beads in a jar) that have little emotional or personal significance (see Freeman,
Note s t o pag e s 2 8 6 – 3 4 1 629
2007; Garety & Freeman, 1999, for review). Although space constraints preclude a full consid-
eration of reasoning in individuals with delusions, it is worthwhile to note here that multiple
factors contribute to delusions, including not only reasoning biases but also the patient’s lack
of awareness and knowledge of internal anomalous experiences and a difficulty in conceiving
alternatives that provide a compelling account of those experiences. Jumping to conclusions is
negatively correlated with what has been termed “belief flexibility”—a metacognitive ability
to generate alternative hypotheses for one’s beliefs and to reflect on the evidence for one’s
beliefs (Freeman et al., 2004; Garety et al., 2005). Environmental factors are also important.
For example, convergent findings in different countries suggest that the frequency of
psychoses is increased in urban compared with rural environments (e.g., Sundquist et al.,
2004), and a recent field study demonstrated that, compared to a nonstressful mindfulness
control condition, even a brief exposure to an unfamiliar stressful urban environment exacer-
bated symptoms such as jumping to conclusions and paranoia in individuals with delusions
(Ellett, Freeman, & Garety, 2008).
3. Although the instructions in the think/no-think paradigm may also elicit reports of
unintended thoughts, this requirement (if given) is superimposed on the ongoing series of
think/no-think trials in which the mental content that is to be focused on or to be excluded
from awareness is itself repeatedly changing.
4. The opera soprano Danielle de Niese has said that she needs to be careful discussing music
late at night because it makes her “manic”: “I start to think about what I need to do better
onstage and how to fix my voice, and one thought bleeds into another, and suddenly I’m
thinking about studies, practicing, contracts, roles coming up, life, and I won’t be able to
sleep all night. I went through a phase when I was listening to music before bed, but now
music reminds me of too many other things.” This is a proactive way of avoiding the need for
thought suppression—by attempting to minimize the cues and associative linkages that
prompt unwanted or untimely thoughts. Quoted in Chip Brown, “Opera’s coolest soprano,”
New York Times, Sept. 16, retrieved May 2011, from www.nytimes.com/2009/09/20/
magazine/20deniese-t.html?_r=1&hpw
5. Although the classic earlier study by George Miller (1956) suggested that most individuals
possess a working memory capacity of approximately seven items (plus or minus two), more
recent research has led to definite downward estimates of this capacity. When researchers
have used tighter experimental control conditions that reduce participants’ ability to rely
on longer term semantic memory and other strategies such as relational encoding to aid
them during working memory tasks, then visual and semantic working memory capacity
have been estimated at approximately four items (e.g., Haarmann, Davelaar, & Usher, 2003;
H. Olsson & Poom, 2005; also see Halford, Cowan, & Andrews, 2007). Capacity may be even
smaller (close to only one item!) when the stimuli to be remembered are highly similar
intracategorical visual items such as composites of similarly colored ovals for which
preexisting semantic representations are of little benefit (H. Olsson & Poom, 2005).
6. Additional findings derived from examining the work processes of so-termed agile program-
ming developers also point to the concurrent use of both elements of rational decision
making (aiming to optimize design) and elements of naturalistic decision making (involving
a “satisficing” goal rather than optimizing goal), with naturalistic decision making tending
to predominate, but supported by rational decision making. See Zannier and Maurer (2006),
“Foundations of agile decision making from agile mentors and developers”; also compare
with the discussion of recognition-primed decision making in the final section of Chapter 2,
including the evidence that surface information is often validly informative and that experts
also may rely on surface information.
Chapter 8
1. For example, Montague and Berns (2002) suggested a model according to which neural
responses in the orbitofrontal-striatal circuit play a role in converting different types of
stimuli and actions into a common scale, to allow comparison of the value of future acts or
630 N O T E S T O PA G E S 341–382
stimuli, with the orbitofrontal-striatal circuit acting as a “common pathway” for the
representation of both rewards and predictors. Specifically, they proposed that the orbit-
ofrontal-striatal circuit “computes an ongoing valuation of potential payoffs (including
rewards), losses, and their proxies (predictors) across a broad domain of stimuli [. . .] By
providing a common valuation scale for diverse stimuli, this system emits a signal useful for
comparing and contrasting the value of future events that have not yet happened—a signal
required for decision-making algorithms that assign attention, plan actions, and compare
disparate stimuli” (Montague & Berns, 2002, pp. 275–276).
2. Here I am reminded of Premack’s (1978) linking of abstractness and concepts of actions.
If one has the concept of “jumping,” then, for example, one may jump a stream in many dif-
ferent ways, depending on the individual, circumstances, inclination, and so on.
Chimpanzees, too, show considerable variation in how they jump. Premack (1978) notes
that there are sketches from van Lawick-Goodale of chimps jumping a stream and landing
not only arms first but feet first and head first. By contrast, the number of manifestations
(or “styles”) of jumping seen in the horse, dog, rabbit, and so on is more limited; one has
never seen them jump a stream backwards, for example.
3. Beyond the anterior to posterior axis, there is accumulating evidence for another functional
gradient in the inferior frontal gyrus or the ventrolateral prefrontal cortex, involving
distinctions in the abstraction and hierarchical level between the anterior versus the
midregions of ventrolateral prefrontal cortex (Badre et al., 2005; Badre & Wagner, 2007;
Gold et al., 2006) and between more anterior and mid- or posterior regions/adjacent to and
including premotor cortex (Koechlin & Jubault, 2006; Poldrack et al., 1999). Badre and
D’Esposito (2007) propose that these other gradients might be more relevant to the retrieval
and initiation of sequences of actions, and the retrieval and organization of lexical, seman-
tic, and phonological codes involved in verbal behavior. For instance, Koechlin and Jubault
(2006) provided fMRI evidence that, within the posterior frontal region broadly correspond-
ing to Broca’s area and its homolog in the right hemisphere, overlearned simple action motor
chunks were associated with more posterior activation whereas superordinate (higher order)
chunks that were also overlearned were associated with more anterior activation.
There also is evidence for hierarchical differences in the processing of language in Broca’s
area (see Bookheimer, 2002, for review, and P. M. Gough et al., 2005, for evidence using
the technique of transcranial magnetic stimulation), such that more posterior regions
(i.e., BA44/BA6) are preferentially recruited for phonological processing (e.g., phonemes
and syllables), whereas more anterior regions are preferentially involved in syntactic pro-
cessing (i.e., BA 45/BA 44) and semantic processing (i.e., BA 47/BA 45), involving words,
phrases, and sentences that are linguistically “higher order.” Gough et al. (2005) note that
this “rostrocaudal division of labor” is consistent with evidence that there are separate
cortico-cortical pathways linking these prefrontal areas to distinct regions in the temporal
lobe, with anterior left inferior frontal cortex linked to temporal pole regions associated
with semantic memory, but the posterior regions connected to temporoparietal regions
involved in auditory processing and speech perception, while a further set of reciprocal
connections between the anterior and posterior left inferior frontal cortical areas allows the
integration of semantic and phonological information.
4. These findings involve systemic effects of tryptophan. Using a procedure that allowed
selective depletion of serotonin in the prefrontal cortex in the marmoset, Clarke and
colleagues (2004) showed that depletion of prefrontal serotonin produced perseverative
responding in a serial visual discrimination reversal task (with no misleading feedback
trials). Notably, this perseverative responding was not accompanied by difficulties in
learning new discriminations postoperatively, and the animals still showed intact discrimi-
nation for stimulus pairs learned preoperatively.
5. Intriguingly, there were also both individual differences and between-trial differences in
whether the activity during the delay period reflected the initial cue stimulus throughout
(a form of retrospective coding, holding the cue stimulus in mind throughout the delay) or
Note s t o pag e s 3 8 2 – 4 0 8 631
if, instead, there was a switch close to the time of the probe stimulus, anticipating the
“correct” associate (a form of prospective coding, representing the anticipated probe
stimulus). These results suggest that this methodology might also provide a potentially
important means of assessing individual differences in strategy use that does not rely only
on self-report.
Chapter 9
1. More specifically, the conceptual topography theory of Simmons and Barsalou (2003)
combines the idea of convergence zones with the “similarity-in-topography principle,”
according to which the proximity of two neurons coding a given conjunction of features or
properties increases with the similarity of the features they conjoin—such that nearby con-
junction neurons code for similar combinations of features. In the theory, besides modality-
specific convergence zones (postulated for visual, auditory, somatosensory, motor,
gustatory, olfactory, and also for emotional processing) and cross-modal convergence zones,
there are also (lower level) analytic and holistic convergence zones that conjoin conjunc-
tions of features (from feature maps) into analytical versus holistic conceptual properties.
2. A related finding, from our own work, is that individuals with semantic dementia show a dis-
proportionate impairment in episodic recognition memory under conditions when many cat-
egorically related items are shown during study (conditions that would benefit from the
extraction of the conceptual commonalities across items) but not when only one item per
category is shown (conditions where recognition memory is more strongly dependent on
item-specific recollection). We found that although patients with semantic dementia showed
significantly lower levels of recognition than did matched control participants for both stud-
ied items and categorically related lure items when many different exemplars from a given
semantic category had been presented, they showed more similar levels of recognition for
items for which only one exemplar had been presented, suggesting they were able to use item-
specific episodic recollection to support their performance to a similar degree as the control
participants (Simons et al., 2005; see Koutstaal & Schacter, 1997a, for additional discussion).
3. One notable exception is the fMRI study by Noppeney and Price (2004), discussed earlier in
this section, contrasting brain regions that were more activated for judgments relating to
abstract than to visual, auditory, or motor-movement judgments. Technical difficulties in
clearly imaging the temporal pole and other brain regions near tissue interfaces (such as air-
filled sinus/brain interfaces) in fMRI arise due to distortions from macroscopic susceptibility
effects, which become more pronounced at higher magnetic field strengths (Devlin et al.,
2000). It is of interest, then, that the study by Noppeney and Price (2004) involved a lower
magnetic field strength (2-Tesla) than used in the direct fMRI versus PET comparison of acti-
vations during a semantic task reported by Devlin et al. (2000, 3-Tesla) and also some other
recent investigations that likewise did not show semantically related modulations in ante-
rior temporal cortex (e.g., Pexman et al., 2007, 3-Tesla). In recent meta-analyses of both PET
and fMRI studies on text comprehension, using the “replicator dynamics” procedure devel-
oped by Neumann et al. (2005), Ferstl et al. (2007, p. 588) observed that “the most striking
result” was “the stability of activation” in the anterior temporal lobes: “In all four analyses,
which were in part based on different studies from different laboratories using different
scanning methods, modalities, and materials, bilateral involvement of this region emerged.”
4. Compare with Tranel (2006, p. 9): “the structures involved in word retrieval, including inter-
mediary structures in left [temporal pole], are not conceptualized as rigid centers; rather,
they are seen as flexible, probability-driven system components [. . .] I contend that in most
individuals, convergence zones involved in various classes of naming tasks are likely to be
found in the same large-scale convergence region of the brain—for example, in left [tempo-
ral pole] in the case of unique names. However, I would not expect that microscale conver-
gence zones would be found in equal sites across individuals. Depending on factors such as
the exact nature of the stimulus, task demands, and the nature of a particular individual’s
632 N O T E S T O PA G E S 408–470
abilities (such as special expertise with certain classes of items), the same task might engage
different convergence zones across relatively comparable individuals.”
5. Grabner et al. (2007) also found a hemispheric effect (right > left) in the upper alpha
frequency band (10–12 Hz), but this effect was not modulated by the self-reported original-
ity of the generated ideas. Thus, there may be higher event-related synchrony in this upper
alpha frequency band in the right cerebral hemisphere during divergent thinking more
generally (rather than especially during the generation of novel ideas).
6. Notably, the momentary lapses of attention were also associated with reduced stimulus-
linked activity in visual processing regions (bilateral inferior occipital cortex), suggesting
that the brief lapses of attention, linked to a reduction in top-down biases signaling to the
sensory cortices, may also result in comparatively low quality representations of stimuli
that are relevant to the task (see also Greicius & Menon, 2004; Smallwood et al., 2009), and
again suggesting a way in which we really do, “think with our senses.”
7. The “somatic marker” hypothesis of A. Damasio (1994) is an important early precursor
within this broad class of accounts that links bodily awareness to social functioning;
however, as noted by Hakeem and colleagues (2009) the more recent accounts place greater
emphasis on the specialized circuitry found within the frontal insular and anterior
cingulate cortices.
8. A third system, the fight/flight system, is not discussed here.
Chapter 10
1. It is important to note that although brain plasticity is often linked to beneficial or positive
outcomes, and such positive effects are the focus in this chapter, not all plasticity is advanta-
geous. Plasticity also may have negative consequences, as in cases of repetitive strain injuries
or repetitive motion injuries and in focal hand dystonia. The conditions that might lead to
negative consequences were clearly delineated by Byl and colleagues (also see Quartarone,
Siebner, & Rothwell, 2006; Wang, Merzenich, Sameshima, & Jenkins, 1995): “In the com-
petitive cortical processes that underly changes induced in learning, the dynamic network
machinery interprets each not-precisely-simultaneous input source as separate and differ-
ent. At the same time, the normal operations of this cortical plasticity machinery can also
lead to degraded representations in the more artificial input circumstances in which afferent
activities are (1) highly repetitive, (2) highly spatially stereotyped, (3) synchronously engag-
ing normally differentiated sensory feedback inputs, and (4) cognitively important, e.g.,
delivered in an attended behavior” (Byl, Merzenich, & Jenkins, 1996, p. 509, original italics).
In an animal learning analog, these researchers demonstrated that two adult New World
owl monkeys that were extensively trained on a repetitive handgrip task developed a move-
ment control disorder. Electrophysiological mapping of the representations of the hand
within the primary somatosensory cortex of the monkeys following the extended repetitive
training showed that the hand representation was markedly degraded; for example, cortical
representations of the skin on the hand were dedifferentiated such that their receptive fields
were 10 to 20 times larger than normal, and there were many receptive fields that emerged
that extended across the entire surface of a digit or across two or more digits. Based on
these and related findings, these researchers suggest that successful treatment of repetitive
strain injuries may require “learning-based restoration of differentiated representations of
sensory feedback information from the hand” (p. 508, emphasis added). As observed later
in this chapter with respect to the high levels of acquired visual-spatial navigational exper-
tise of London taxi drivers (see note 2), plasticity in the hippocampus, involving a shift in
the relative distribution of grey matter volume from anterior to mid-posterior hippocam-
pus, may also be associated with decrements in acquiring other forms of novel visuospatial
and associative information.
2. Additional findings suggest that the reorganization observed in highly expert taxi drivers
may carry with it some cognitive costs, specifically with respect to the ability to acquire and
Note s t o pag e s 4 7 0 – 4 8 7 633
cognitive function (e.g., higher idea density was associated with less cognitive impairment)
and several neuropathological measures. Lower idea density was associated with lower brain
weight, a higher degree of cerebral atrophy, more severe neurofibrillary pathology, and an
increased likelihood of meeting neuropathologic criteria for Alzheimer’s disease. Particularly
given the relative similarity of the adult lifestyles of this population these very early differ-
ences argue that factors “responsible for poor performance earlier in life contribute to both
levels of education and to the subsequent development of impairment” (Milgram et al.,
2006, p. 356).
9. An additional source of evidence for the potential protective effects of education derives
from the consideration of other conditions that may lead to dementia, such as AIDS.
Satz et al. (1993) examined the effects of educational level in sero-positive men on neuro-
psychological function. Approximately 10% of the cohort had 12 grades of education or less,
whereas the remainder of the cohort had higher education. Cognitive abnormality was
defined as performance that was 2 or more standard deviations below the mean for the total
group on at least one of five neuropsychological tests (Grooved Pegboard, Verbal Fluency,
Digit Span, Symbol Digit Modalities, Rey Auditory Verbal Learning). Whereas the perfor-
mance of 38% of those with no more than 12 years of education met this impairment
criterion, fewer than 17% of those in the higher educational level group showed impair-
ments of this magnitude, and this effect remained after statistically controlling for the
possible confounding effects related to such factors as age, race/ethnicity, depression, prior
drug history, and learning disability.
10. See also note 8 in this chapter for evidence relating to this issue derived from the longi-
tudinal study on Alzheimer’s disease conducted with Catholic nuns (Riley et al., 2005;
Snowdon et al., 1996).
11. The index of flexible thinking was based on seven measures, including: performance on an
embedded figures task; two indices from a projective task (the Draw-A-Person test); the
judged adequacy of the participant’s responses to questions asking (a) for arguments for
and against allowing cigarette commercials on television, and (b) factors to consider, from a
business perspective, in choosing between two potential locations for a hamburger stand;
the overall number of “agree” responses during the interview; and interviewer ratings of
the individual’s intelligence. Nearly all of these measures include a strong subjective compo-
nent and are susceptible to biases from the examiner.
12. Presumably because education strongly correlated with the substantive complexity of the
occupations achieved, when education was included as a covariate, substantive complexity
was no longer predictive.
13. In a Japanese 10-year longitudinal study, cognitive decline in men as assessed by a short-
term visual memory test was also predicted by occupation of longest duration, with individ-
uals in blue-collar occupations showing greater decline on this measure than shown by
those in white-collar occupations (Deeg et al., 1992).
14. Relatively specific positive transfer benefits from the frequent engagement in solving cross-
word puzzles to a task of anagram solution were reported by Witte and Freund (1995,
Experiment 2): Whereas for infrequent solvers of crosswords, younger adults’ anagram
solution performance significantly exceeded that of older adults, there was no age differ-
ence in anagram solution performance for younger versus older adults who reported engag-
ing in crossword puzzles once a week or more.
15. Recent work using a chronic stress paradigm with rats (Dias-Ferreira et al., 2009) has also
shown that chronic stress may induce changes in fronto-striatal organization, such that
stressed animals showed atrophy of the associative corticostriatal circuits but hypertrophy of
the circuits running through the sensorimotor striatum. Chronic stress biased the animals
to respond on the basis of habitual strategies and decreased their ability to flexibly alter
their habitual behavior when the consequences of their behavior (e.g., a change from
a palatable reward to a degraded reward) changed, even though both control and stressed
animals showed that they preferred the nondegraded food. As the authors note, “the more
Note s t o pag e s 5 1 8 – 5 3 6 635
rapid shift to habits after chronic stress could be a coping mechanism to improve perfor-
mance of well-trained behaviors, while increasing the bioavailability to acquire and process
new information, which seems essential for adaptation to complex environments. [. . .]
However, when such objectives need to be re-updated in order to make the most appropri-
ate choice, the inability of stressed subjects to shift from habitual strategies to goal-directed
behavior might be highly detrimental” (Dias-Ferreira et al., 2009, p. 625). If chronic stress
similarly biases cognitive processing toward habitual or automatic responding in humans,
whether children or adults, this might also contribute to diminished mental agility. For the
clear detrimental effects of a preference for what is familiar under short-term sources of
pressure, such as time pressure, or pressure to reach a performance benchmark, see Litt
et al. (2011).
Chapter 11
1. Effects of enriched environments on the adult primate brain have also been demonstrated.
In particular, Kozorovitskiy et al. (2005) found that moving adult marmosets (New World
monkeys) from standard laboratory conditions to a complex environment for 1 month was
associated with increased dendritic spine density, dendritic length, and dendritic complex-
ity of neurons in the hippocampus and the prefrontal cortex. This study did not, however,
include behavioral measures, so the extent to which these brain changes in the primate
influenced cognitive-behavioral performance is unknown.
2. A very early, but clearly less controlled, demonstration of the increased flexible problem-
solving abilities of animals raised in an enriched compared to an impoverished environment
was reported, in 1947, by D. O. Hebb. Hebb compared the on-the-spot problem-solving abil-
ity of 25 normal rats reared in laboratory cages, to that of 7 rats that were reared at home as
pets, with much of their time spent outside of their cages. He reported that there was a
“definite [. . .] superiority of the group with the greater infant experience.” Based on these
and related data, Hebb reached two important conclusions: “1. There is a lasting effect of
infant experience on the problem-solving of the adult rat. 2. This difference may not be
detectable in rote learning scores, but appears when a method is used that is more like a
human intelligence test: that is, with an index based on a large number of problems which
some normal animals solve promptly” (Hebb, 1947, p. 307).
3. Most intriguingly, these researchers (Kolb et al., 1998) observed a similar dissociation of
changes in dendritic length versus dendritic spine density in an environmental enrichment
study in which they lesioned the hippocampus of rats on one side of the brain (unilateral
lesions), but left the hippocampus on the other side of the brain intact. Whereas the hip-
pocampus that was still intact showed both enrichment-related increases in dendritic length
and an increase in spine density, the lesioned hippocampus showed increases in dendritic
length together with a decrease in spine density, as though the lesioned portion of the brain
was responding more like the immature hippocampus of a younger animal.
4. These positive results, reflecting improved problem solving in a novel context, contrast with
findings reported by K. R. Light et al. (2008) in which, although repeatedly exposing
juvenile or young-adult mice to novel environments (e.g., 12 different novel environments
for 20 minutes per day over a period of 14 days) did promote the animals’ subsequent
exploratory behaviors (e.g., in an elevated plus maze), novel environmental exposure had
no effect on subsequent measures of the animals’ general learning performance (assessed by
a battery of five tasks, including Lashley maze, passive avoidance, spatial water maze, odor
discrimination, and associative fear conditioning). These researchers further found
that repeated exposure to a single different environment (apart from the home cage) also
bolstered exploratory behaviors, but likewise did not influence general learning. It is possi-
ble that, with more extensive or prolonged exposures to the novel environments, effects on
general learning might have been found. Additionally, however, one notable difference
between the two paradigms involves whether animals were reinforced for variable behavior;
636 N O T E S T O PA G E S 536–551
reinforcement of variable behavior may have imposed working memory demands on the
animals, as successful variation of responding will be facilitated by keeping track of, and
updating, information about recently emitted responses (Neuringer, 2004; also cf. Mercado
et al., 1998).
In more recent work, K. R. Light et al. (2010) found that training mice in a task placing
strong demands on working memory (navigating two eight-arm radial arm mazes that
shared common extramaze visual cues for reward) did promote general cognitive perfor-
mance. Furthermore, this beneficial outcome was attenuated (but not eliminated) if the
working memory training posed fewer demands on selective attention, because the two
mazes each had separate, nonoverlapping, rather than shared, extramaze cues. These
findings provide important convergent support for earlier findings, obtained with human
participants, and discussed in later sections of this chapter, that working memory training
can lead to generalized improvements on never-trained tasks, such as measures of fluid
reasoning. Based on other (in progress) work, Light et al. (2010) speculate that the working
memory training may have up-regulated the expression of a cluster of genes related to
dopamine signaling in the prefrontal cortex.
5. As developed in the final section of this chapter, in our lab (Tranter & Koutstaal, 2008), we
also earlier demonstrated significant improvements on a measure of fluid reasoning in older
adults; specifically, experimental assignment to 10–12 weeks of increased engagement in
novel home and in-lab activities led to a significant pre-post increase in Cattell Culture Fair
scores, compared with the pre-post difference found in a social contact control group.
6. See, for example, Draganski et al.’s (2006) research examining structural changes in the
brain arising from medical students’ intensive preparations for medical examinations.
7. Blocking BDNF action also prevented an exercise-induced increase in CREB mRNA levels
and in synapsin I mRNA levels. Vaynman et al. (2004) therefore suggest that exercise might
lead to enhanced memory consolidation by facilitating the expression of CREB, which is
believed to be essential for long-term memory formation, and also (through synapsin I) by
boosting reserves of synaptic vesicles. See Vaynman et al. (2004) for additional details.
8. Nonetheless, a meta-analysis of a range of cognitive training interventions in Alzheimer’s
disease provides tentative grounds for supposing that cognitive training also may be benefi-
cial in such cases (Sitzer, Twamley, & Jeste, 2006). Interventions that involved so-termed
“restorative strategies,” such as general cognitive stimulation (e.g., problem-solving, reading,
engaging in creative activities) or computerized visual-spatial drills were found to be more
effective (average effect size d of 0.54) than were “compensatory strategies” (average effect
size d of 0.36) aimed at circumventing impairments (e.g., through taking reminder notes).
Although the beneficial effects of cognitive training were greater in studies that did not use
an attention-placebo control condition than in those that did, this may itself actually under-
score the benefits of increased cognitive stimulation, as in these studies the attention-pla-
cebo control condition participants may also have benefited from the modest increase in
stimulation they received, and this could act to attenuate differences between the groups.
Animal work using transgenic mice also broadly suggests that increased environmental
stimulation may be beneficial in dementia: Compared with standard-housed mice, trans-
genic mice co-expressing familial Alzheimer’s disease-linked APP and PS1 variants that were
housed in enriched environments showed reduced cerebral B-amyloid peptide levels and
reduced amyloid deposits, and selective up-regulation in levels of transcripts encoded by
genes associated with (among others) learning and memory and neurogenesis. See Lazarov
et al. (2005) for details.
9. See Willis and Nesselroade (1990), for a study that meets some of these concerns.
Unfortunately, however, the training benefits they report from multiple phases of cognitive
training are confounded with specific practice on the materials used at pre- and posttest to
assess treatment gain.
10. One noteworthy study that involved training older adults in the method of loci over a
5-week period not only found significant behavioral improvements but also found, using
Note s t o pag e s 5 5 1 – 5 6 3 637
by Olesen, Westerberg, & Klingberg, 2004). In the Klingberg et al. study the participants
were children between the ages of 7 and 15 years who had been diagnosed with attention-
deficit/hyperactivity disorder. Generalization of training benefits to tests of abstract rea-
soning in these experiments and also in a further experiment using the Advanced
Progressive Matrices with adults with attention-deficit/hyperactivity disorder (Experiment
2 of Klingberg et al., 2002) may reflect common demands on prefrontal networks for the
control of attention and of working memory. Although matrices are only one form of fluid
intelligence measure, they are a highly central measure; the across-study and across-popula-
tion improvements on this measure as a result of training in attention and working memory
argue against conceptions of “fluid intelligence” as a fixed quantity; rather, fluid intelligence
is also shaped by ongoing environmental stimulation and challenges (cf. C. Schooler, 1998).
16. Luria (1965), for instance, provides several examples of the directive meaning of words fail-
ing to influence the child’s behavior (e.g., to “take off the ring” rather than to “put on the
ring”), even though the child does “know” the meaning of the words—but the words con-
flict with the child’s own immediate motor activity, sensory input, or previously repeated
motor actions. He observes that “The directive role of the word at an early age is maintained
only if the word does not conflict with the inert connections which arose at an earlier
instruction or which began with the child’s own activity” (p. 353), and that phrases such as
“Don’t press the ball” have both a semantic aspect (pointing to abstaining from pressing)
and an immediate impulsive impact (that conflicts with abstaining from pressing, and
instead, leads to pressing). Only gradually does the semantic aspect become sufficiently
strong to counteract the impulsive impact; often, at this point, and typically at the age of
about 4 or 4½ years, “external speech becomes superfluous” (p. 362).
17. These social group meetings helped to maintain the control participants’ interest in the
study and also increased their familiarity with the testing location, thereby providing a
tighter and fairer comparison for the experimental group than would a simple pre-post test
only comparison group. Notably, once participants had committed to the research, there
was very little attrition from the study, with only one participant being lost from the experi-
mental group.
Chapter 12
1. In his autobiography, A Jazz Odyssey: My Life in Jazz and in interviews, the jazz pianist Oscar
Peterson (2002) noted the vast potential for involvement in illicit drugs and excessive alco-
hol use among the musicians, particularly given the many weeks that they needed to be on
the road, away from home, with accompanying periods of loneliness, boredom, and so on.
He also pointed to his passion for photography as helping him to avoid more dangerous
diversions—even traveling with his own darkroom, to which he often would retire to
unwind after the intense late-night gigs.
2. See, for example, P. J. Taylor et al. (2010), for findings showing that, in a group of psychotic
outpatients with schizophrenia spectrum disorders, even after controlling for depressive
symptoms and trait anxiety, more specific autobiographical memory was predictive of
increased suicide attempts, and that the attempters also found a greater proportion of spe-
cific memories currently distressing. Also see Swales, Williams, and Wood (2001) for evidence
that, within an adolescent clinical sample, repeatedly retrieving specific memories—giving
the same specific memory to multiple cues, and often involving a traumatic memory—was
significantly associated with a history of parasuicide.
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Index
Note: Page numbers followed by f, n, or t indicate content found in figures, notes, and tables, respectively.
739
740 INDEX
making v. finding by, 29–30, 327, 332–34, 595 habit-based, 91–98, 617n4
motivation and, 220, 230–31, 234–37 hierarchies of gist and, 39–41
works completed by, 624n1 “if, then” conditional rule and, 37–39, 95, 309
associative learning, 367 instance theory of, 35–37
Associative v. Rule-based processing, 16 levels of specificity and, 91–98
attention in object naming and identifying , 135–36
BIS and, 452 in remembering intentions, 187–90
concentrative v. receptive, 93, 121–22 repetitive, 601–6
conceptual, 451 strategic automatization, 190, 600
creativity and, 44, 117–22, 614n5 in theory of event coding , 36–37, 367
deliberation without, 313–14 verbal fluency and, 372–73
directed, 559 word association and, 73
ego depletion and, 203 worry and, 618n10
executive, 375 automatic optimism, 291
in focused attention meditation, 93 automatic writing, 49–50, 175–76, 616n11
importance of, 42 avoidance orientation
restoration, 201, 559–62, 583, 588, 592–94 approach orientation v., 11, 388, 451–60, 455f
training BIS aligned with, 453
in children, 562–67 avoidance theory of worry, 68–69, 288
direct effortful, 592–94
experimental interventions, 554–59, 562–67
flexibility improved by, 562–67 balanced time perspective, 199–200
less directed, 592–94 BAS. See Behavioral Activation System
oscillatory range and, 592–94 basic-level naming advantage, 401–2, 403f
video gaming and, 554–59 BDNF. See brain-derived neurotrophic factor
pupil dilation in, 279 behavior
unfocused, 91, 117–22, 315 appetitive, 228
voluntary, 559 consumatory, 228
Attention Network Task, 561 correlational structure of, 342–43
attunement, 68, 132, 161, 410, 579, 601 data-driven, 325
auditory association cortex, 391 foraging, 225
autism, 616n1 instrumental structure of, 342–43
autobiographical memory intentions differing from, 260
AJ’s, 55, 58, 67, 616n3 plasticity influencing , 463–68, 466f
default network and, 431 suicidal, 62, 602–3, 638n2
elements of, 33 variability of
hierarchical structure of, 60–62, 61f controlled, 227–29
overly general, 60–63, 66–68, 67f in natural selection, 226–27
suicidal behavior and, 62, 602–3, 638n2 reinforced, 45, 222–24, 227–29
automatic cognitive modes. See also integrated Behavioral Activation System (BAS), 452–58, 455f
Controlled-Automatic, Specific-Abstract behavioral cusp, 598
framework behavioral engagement, emotions and, 239–40, 240f
ACT-R model and, 36–39 behavioral extinction, 227–29, 626n13
benefits of, 21–22 Behavioral Inhibition System (BIS), 452–58, 455f
in controlled-automatic distinction, 54, 139–41 belief
convergent theoretical perspectives on, 35–41 epistemological, 283–85, 329, 599
deautomatization and, 95–96 flexibility, 628n2
deliberate v., 15, 318–22 Big Five personality dimensions, 192–93, 627n3.
ease of construing objects and events at different See also five-factor model of personality
levels of specificity and bilateral activity, increasing with aging, 475–78
effects of emotion on categorization, 105–7 bilingualism, 507–13, 509f
environmental and contextual determinants of BIS. See Behavioral Inhibition System
action identification, 101–3, 106–7 blood glucose levels, 206–7
overview of, 101 body-mind training , 97–98
psychological or temporal distance effects on bootstrapping
construal level, 103–7 abstraction, 80, 83–87
flexibility and, 21 flexibility in noticing and, 144
fuzzy trace theory and, 36, 39–40 bottlenecks, in processing, 36, 38
goals and, 21, 304–5, 617n4 Braille reading, 464–65
742 INDEX
brain. See also specific structures broaden and build theory, 242, 250, 278, 280, 317,
activity, nature of, 388 369, 607
adaptive character of, 633n3 broad minded affective coping procedure, 606
bases, of mental agility burnout, 588–89
across-system interactions, 374–86, 378f,
383f, 388
of adaptive responding to novelty, 445–51, 448f candle problem, 127, 244, 621n2
of amodal representations, 395–96, 399, cardiovascular fitness, 512–13, 546–48
404–5, 408, 410 cascade architecture, 352–53, 353f
of analogical thought, 410–14, 411f cascade view, of aging , 484–85, 484f
anterior-to-posterior interactions, 374–86, categorical memory, overly abstract, 43–44, 60–68,
378f, 383f, 388 61f, 67f
approach v. avoidance, 11, 388, 451–60, 455f categorization
of conceptual representation, 389–410, 396f, adaptive
402f–403f abstract, rule- or category-based knowledge
fluid intelligence and, 374–86, 378f, 383f and, 79–89, 85t, 89t
goal neglect and, 374–86, 378f, 383f highly detailed specific instances and, 79–89,
implications, 579 85t, 89t
of insight, 417–18, 420–28, 421f, 423f physical embodiment and, 81
of intuition, 417–19 ad hoc or goal-derived, 71–72, 133
noradrenaline in, 414–17 analogical thinking and, 112–13
of oscillatory range, 439 flexible abstract representation of, 344–52, 345f,
overview of, 46–48, 337–38, 386–88, 460–61 347f–348f
of relational thought, 410–14, 411f in Halstead Category Test, 56
of resilience, 388, 439–45 microcategorization, 113
resting states and, 428–39, 438f negative emotion influencing , 451–52
spontaneity and, 388 positive emotion influencing , 105–7, 250,
of thinking with senses, 389–410, 396f, 451–52
402f–403f social, 327–28
working memory and, 374–86, 378f, 383f visual, by monkeys, 344–52, 345f, 347f–348f
bilateral activity, in older persons, 475–78 in weather-prediction task, 481
competition among regions, 633n5 in Wisconsin Card Sorting Task, 55–56, 138–39
conceptual knowledge locations in, 126, category-based knowledge
390–91 adaptive categorization and, 79–89, 85t, 89t
fluid reasoning correlates, 410–14, 411f cognitive fluency task requiring, 71–75
functional and connectivity mapping of, 30–35, overreliance on, 98–99
32f, 35f of recently experienced events, 78
paths, to mental agility category-based retrieval cost, 99, 620n4
bilingualism and multilingualism, 507–13, 509f Cattell Culture Fair test, 30, 75, 78, 375, 568–69
cognitively stimulating leisure activities and, central executive networks
499–506 default network interacting with, 34, 35f, 117,
environmental stimulation and, 486–504, 388, 433–35, 577–80
489f, 491f, 493f, 527–38, 530f, 532f, 534f functions of, 27–28, 67
experimental interventions, 539–69 neural mechanisms, 577–80
multidimensional interventions in community, salience networks interacting with, 25, 34,
521–25, 524f, 595–96 35f, 435
overview of, 462–63, 526–27, 569–72 children
physical exercise and, 512–13, 546–48 attention training in, 562–67
plasticity in, 463–86, 466f, 474f, 483f–485f with autism, 616n1
socioeconomic status and, 482, 513–21, 517f Child Attention Network Test for, 563–64
reserve exercise needed by, 585
cognitive reserve compared to, 473–74, 497 functional fixedness in, 127–31
compensation and, 471–86, 474f, 483f–485f naivety advantage and, 128–130
conditions related to, 633n4 poverty and, 514–21
passive models of, 472 recess and, 584–85
schematic rendering of, 474f rules acquisition by, 23–24
threshold in, 471–72 self-regulation by, 564–65
brain-derived neurotrophic factor (BDNF), 548 Tools of the Mind program for, 565–67
breadth-first strategy, 325–26 choking under pressure, 307–8
I n dex 743
contextually linked learning, 618n13 cortical maps, plasticity of, 463–68, 466f, 632n1
contrastive learning approach, 109 creativity
control. See also Adaptive Control of Thought– association horizons and, 415
Rational model; integrated Controlled- attention and, 44, 117–22, 614n6
Automatic, Specific-Abstract framework; biological bases of, 614n6
levels of control environmental enrichment and, 230
action, 180–90 everyday, 243
of behavioral variation, 227–29 executive networks–default mode interactions
continuum of, 4 influencing , 577–80
controlled-automatic distinction, 36–39, 54, failure and, 626n14
139–41 gating of stimuli and, 426–27
controlling of, 451–60, 455f hypomania influencing , 245–46
effortful importance of, 597–98
limits of, 21–22 mental agility distinguished from, 4, 5f, 29–30
motivation and, 194–98 mind popping and, 117–22
orienting sensitivity and, 273 motivation and, 217–20
stability of, 625n5 openness to experience and, 269–78, 628n6
ego, 29, 191–94 opportunistic design and, 326
episodic, 353–54 in problem solving, 112–17, 598–606
executive, 27–28, 305–6 reinforcement of variability influencing , 228,
frontal cortex and, 338–43 597, 625n10
intentions and, 187–90, 298–307 remote alternatives in, 244–45, 414–17
minimal control principle, 38 rewarded, 218–20
negative control effect, 300 schedules maximizing , 584–92, 586f–587f
overcontrol, 29, 192–93, 196, 198–201, 615n8 in workplace, 212, 219
prefrontal cortex and, 338–43 critical incident training approach, 110
of processing, 30, 45, 54, 372–73 crossword puzzles, 496, 634n14
reactive, 194–98 cultural factors, 41
resiliency and, 197 cumulative-hierarchical learning , 598
self-control, 195–99 curiosity, 198, 214, 278–80, 284–85, 594
semantic, 408
sensory, 352–54
temporal, 353–54 dance, 596
thinking with senses and, 139–41 day-to-day schedules, for maximizing creativity and
of thought learning , 584–92, 586f–587f
controlled losing of, 307–13, 311f deautomatization, 95–96
diversity and, 327–29 decentering, 95–97
environment and, 329 decision making
flexible thinking and, 283–85 beads task and, 286–87, 628n2
incubation, complex decision making and, complex, incubation and, 313–22
313–22 intuition in, 613n4
intentional forgetting and, 298–307 myopia in, v. hyperopia in, 200
intolerance of uncertainty v. ambiguity, openness to experience influencing, 276–77, 277f
285–91 recognition-primed, 86, 613n3
learning to learn and, 283–85 unconscious processing and, 317–22, 613n4
movement between higher and lower level unfocused attention and, 315
goals, 323–27, 323f–324f declarative memory, 37–38
noncontrol v., 282–83 decline-compensation view, of aging , 484, 484f
optimism v. pessimism, 291–98 dedifferentiation, 475–77
overconfidence v. underconfidence, 291–98 default network. See also salience network
overview of, 282–83, 329–30 anxiety and, 435
self-affirmation influencing, 262–66 autobiographical memory and, 431
convergence zones, 395, 582, 631n1, 631n4 central executive network interacting with, 34,
coping strategies 35f, 388, 433–35, 577–80
for breast cancer surgery, 293 defined, 428–29
broad minded affective coping procedure, 606 depression influenced by, 433
Krohne’s model of, 288, 290 functional roles of, 430–31
positive well-being enhanced by, 254 gateway hypothesis and, 430
self-affirmation, 258 neural mechanisms, 577–80
I n dex 745
resting states and, 428–39, 438f fuzzy trace theory as, 14, 39
salience network interacting with, 34, 35f, 435 intuitive processing and, 17–23
simulations influenced by, 432–33 overview of, 15–16
subsystems, 431–32 difficulties with, 17–22
defensiveness, 258–60 dual-task variable-priority training , 554–59
deliberate cognitive modes dynamic affect model, 252–53
without attention, 313–14
automatic v., 15, 318–22
thought suppression and, 298–307 education
deliberate practice, of agile thinking, 549–51 dementia influenced by, 487–94, 489f, 491f,
dementia 493f, 634n9
in Alzheimer’s disease, 487–94, 489f, 491f, 493f, environmental enrichment influencing , 487–94,
498–505, 510, 513 489f, 491f, 493f
bilingualism influencing, 510 epistemological beliefs and, 284, 606–08
cognitively stimulating leisure activities and, iCASA implications for, 606–12
499–506 measurement of, 488–89
education influencing, 487–94, 489f, 491f, 493f, effortful control
634n9 limits of, 21–22
occupational factors in, 498 motivation and, 194–98
physical exercise influencing, 513 orienting sensitivity and, 273
semantic, 397–401, 404, 410, 631n2 stability of, 625n5
defined, 616n2 ego control, 191–94
frontal variant contrasted with, 411–12, 411f ego depletion
stroke aphasia compared to, 407–8 attention and, 203
social interactions and, 494–96 executive function and, 204–5
twin studies of, 490, 491f illustrations of, 202–3
dentate gyrus, 531, 596 motivation and, 45, 201–14
depression See clinical depression ego resiliency, 191–94, 200–201
depth-first strategy, 325–26 Embedded Figures Task, 72–73, 618n12
design stance, 130–34 emotional complexity, 254–55
detectives, 142, 174–75 emotional empathy, 199, 405, 432
developmental psychology, 23–25, 128 emotions
devil’s advocate, 608 abstract content and, 12–13
dietary restraint, 202–3 behavioral engagement and, 239–40, 240f
directed attention, 559 boundaries of, 8
directed forgetting, 298–307 cognition’s interplay with, 19, 20f, 451–60, 455f
direct effortful attention training, 592–94 concept interpenetration with, 598–606
direct instructions, 574 goals influenced by, 239–40, 457–58
discontinuity, in adaptability, 471 granularity of, 251–57
discovery, context of, 22 inferred, 404–5
distributed-only view, of concepts, 395–97, 396f interest as, 278
distributed-plus-hub view, of concepts, 395–97, joy, 278
396f, 399–400 meta-emotions, 604
divergent thinking, openness to experience and, negative
270–75 broad minded affective coping procedure and, 606
diversity error-related, 453–54
discussion of, 584 influence of, 239, 248–49
functional, 327 mood clarity and, 254–55
in thoughts and views of others, 327–29 narrower categorizations and, 451–52
DLPFC. See dorsolateral prefrontal cortex positive emotions interacting with, 252
dopamine, 362–66, 371–72, 545–46 self-sustaining feedback loop of, 305
dorsal anterior cingulate cortex, 434–35, 577–78 overview of, 238–39
dorsal raphe nucleus, 444 positive
dorsal ventromedial prefrontal cortex, 432 Alternative Uses Task influenced by, 244, 246
dorsolateral prefrontal cortex (DLPFC), 35f broad minded affective coping procedure
dual motivation, 234–37 and, 606
dual-process mode categorization influenced by, 105–7, 250,
hypothesis of self-awareness, 604–5 451–52
theories flexibility influenced by, 45, 243–51
746 INDEX
Experiential subsystem, Rational subsystem v., 16 flexibility. See also spontaneous flexibility
experimental interventions abstract content and, 79–89, 85t, 89t, 344–52,
using Alternative Uses Task, 71–75, 618n11 345f, 347f–348f
attention restoration theory and, 559–62 in accessing semantic knowledge, 75
attention training, 554–59, 562–67 attention training improving , 562–67
for brain paths to agility, 539–69 automatic cognitive modes and, 21
difficulty level of, 572 belief, 628n6
natural environment, 559–62, 583 category-based knowledge and, 79–89, 85t, 89t
physical exercise and cognitive performance, constrained, 416–17
546–48 control of thought and, 283–85
playful practice, 567–69 definitions of, 29–30, 614n5, 634n11
practicing agile thinking, 549–51 frontal cortex and, 338–43
recently acquired expertise and brain plasticity, highly detailed specific instances and, 79–89,
539–46 85t, 89t
recollection training, 551–54 intentional forgetting and, 298–307
summary of, 48, 570–72 neurocomputational, 473–74, 474f
thinking with senses and, 572 neurotransmitters and, 362–66, 371–72
using self-affirmation, 264, 269 in noticing, 143–44
video games and, 556–559, 637n12 occupational factors, 496–99
expertise, recently acquired positive emotions influencing , 45, 243–51
juggling , 540–42 prefrontal cortex and, 338–52, 345f, 347f–348f
of pianists, 539–40, 545 reactive, 370–71
plasticity and, 539–46 in remembering recent events at differing levels
working memory training, 543–46, 637n15 of specificity, 75–78
expertise-based approach, to intuitive rules and, 24–25, 79–89, 85t, 89t, 344–52, 345f,
processing, 17 347f–348f, 575
explicit instructions, 107–11, 574 self-affirmation and, 257–69, 267f
exploration stability trade-off with, 370, 531
of environment, 26–27, 225, 387–88, 635n4 thought suppression and, 298–307
exploitation and, 446, 597 unconstrained, 416–17
by problem-explorers, 549 whole person influencing , 44–46
extension memory, 247–48 flexible remembering , 78
external regulation, 216 flow, 307–13, 311f, 593
extinction, 227–29, 626n13 fluency effects, 169–73
extraversion, 239, 269, 273–74 fluid intelligence
extrinsic motivation, 214–18, 220, 229, 234–37 brain bases of mental agility and, 374–86,
eyes, mind guided by, 147–52, 147f 378f, 383f
executive attention and, 375
interventions to improve, 74–75, 97–98, 264,
failure, creative approach to, 608, 626n14 544, 567–69
fascination, 560, 594, 637n13 mental agility distinguished from, 4, 5f, 30
feedback-mediated learning, 364, 449 openness to experience and, 627n5
feelings-as-information model, 243 resource depletion and, 212
finding. See making and finding shaping of, 502, 637n15
five-factor model of personality. See also openness working memory and, 375, 615n7, 637n15
to experience fluid reasoning, 636n5
agreeableness in, 269 brain correlates of, 410–14, 411f
conscientiousness in, 269, 627n4 flexibly remembering recent events at differing
defined, 192, 627n3 levels of specificity and, 75–78
extraversion in, 239, 269, 273–74 interventions to improve, 74–75, 97–98, 264,
meta-analyses of, 274 544, 567–69
plasticity and, 239, 274 subcognitive mechanisms of, 122–24
resilience and, 192–93 focused attention meditation, 93
stability in, 239, 274 forgetting
fixation. See also functional fixedness directed, 302, 298–307
dissipation of, 118 ethics and, 610–12
exemplar-based, 118–19 fixation, 315–17
forgetting, 315–17 importance of, 610–11
fixed intelligence, 284, 606–7 intentional, 298–307
748 INDEX
form, meaning and, 167–69 categorization derived from, 71–73, 75, 133
frontal cortex emotion influencing , 239–40, 457–58
abstraction and, 338–43 higher and lower level, movement between,
flexibility and, 338–43 323–27, 323f–324f
hierarchical and functional distinctions within, instrumental, 343
352–59, 353f, 357f–358f learning influenced by, 284
lesions, 361, 370–73, 449 motivation and, 184–85
levels of control and, 338–43, 358–59 neglect, 139, 374–86, 378f, 383f
levels of specificity and, 339–40, 358–59 open, 185–90, 317
medial orbital, 418–19 positive emotions and, 239–40
parietal cortex interacting with, 377 prefrontal cortex and, 456–57
role of, 58–60, 59f, 151, 338–43 working memory influencing , 457–58
spontaneous flexibility and, 359–73 granularity
frontal pole. See rostrolateral prefrontal cortex defined, 11
frontostriatal system, 58, 195, 371, 617n4, 629n1, of emotions, 251–57
634n15 varying levels of, 11–12, 15
functional and connectivity mapping, of brain, granule cells, neurogenesis of, 530–35, 530f,
30–35, 32f, 35f 532f, 534f
functional avoidance, 66, 602
functional fixedness
defined, 14, 118 habits
priming and, 127–28 automatic, mindfulness training reducing, 91–98
thinking with senses and, 127–33 cortico-striatal bases of, 617n4, 634n15
fuzzy processing preference, 40 fostering, 600
fuzzy-to-verbatim continua, 12 habit-based blindness, 128
fuzzy trace theory reperceiving and, 95–97
automaticity and, 36, 39–40 self-regulatory depletion and, 202
as dual-process account, 14, 39 stereotypy of responding in, 544
levels of specificity and, 14 useful variation in, 597–98
hardiness, 253–54, 274, 608
HAROLD. See Hemispherical Asymmetry Reduction
gambling task, 361, 613n4 in OLDer adults
generalized anxiety disorder, 69, 288 healthy skeptic, 558, 608
General story source problem, 145 Hemispherical Asymmetry Reduction in OLDer
gestures adults (HAROLD), 475, 478
indexical hypothesis of, 157–58 Hemispherical Encoding Retrieval Asymmetry
during learning, 156–57 (HERA) theory, 475, 478
organizational structure and, 160 hemispheric differences, 421–22, 428, 580, 632n5
during problem solving, 154–56 HERA theory. See Hemispherical Encoding
in science laboratories, 157, 622n9 Retrieval Asymmetry theory
speech and, 154–55 heterarchical organization, 33
thinking with senses and, 154–61 heuristics
types of, 154, 622n8 affect, 19, 291–92
visual-spatial aspect of, 157 in cognitive-experiential self-theory, 16
working memory influenced by, 159–60 fluency, 170–173
gist recognition, 613n3
bias toward, 551 use of, 22, 137, 615n10
capturing of, 40–41 heuristics and biases approach, 17–18
hierarchies of, 12, 39–41 hierarchical organization
intuition and, 417–19 of autobiographical memory, 60–62, 61f
memory and, 53–54, 615n9 cumulative-hierarchical learning and, 598
overreliance on, 98–99 in executive memory, 33
sensitivity to, 100 in frontal and prefrontal cortex, 352–59, 353f,
global processing default bias, 248 357f–358f
glucose levels, 206–7 language and, 630n3
goal(s) models of action control and motivation, 180–90
artist’s, 332–34 of relations, 116
automatic activation of concepts in relation to, hierarchies of gist, 12, 39–41
304–5 higher order rules, 23–24
I n dex 749
uncertainty
equivocality v., 331 WCST. See Wisconsin Card Sorting Task
intolerance of, 285–91 Wechsler Adult Intelligence Scale, 56, 78, 379
unexpected, 445–46 weighted additive rule, 615n10
unconstrained flexibility, 416–17 white bear thought suppression approach, 302–3,
underconfidence, overconfidence v., 291–98 307, 330
unexpected uncertainty, 445–46 willpower, 208, 609–10
unfocused attention, 91, 117–22, 315, 614n6 Wisconsin Card Sorting Task (WCST), 416–17
“use it or lose it” hypothesis, 463, 503, 534f, categorization in, 55–56, 138–39
567–69 novelty in, 448–49
word(s), 582, 631n4
association, 72–73, 245, 618n12
vacation, 200, 588–89, 592, 625n6 cohort activation of, 167–69
values, 609–12 directive meaning of, 638n16
values affirmation, context-dependent effects fluent perception of, 169–73
of, 576 indexical hypothesis and, 162
variability innovative uses of, 161–62
of behavior meaning and form of, 167–69
controlled, 227–29 repetition and rhyming of, 170–73
in natural selection, 226–27 in Scrabble, 163–64
reinforced, 45, 222–24, 227–29 in thinking with senses, 125, 166–73
generalized, 224, 618n11 in writing process, 165–66
response, 225–26 working memory
stability integrated with, 229–33 in aging and upregulation of, 478
in strategy use, 232 bilateral parietal cortex and, 377
training in, 221–24 brain bases of mental agility and, 374–86,
variable-priority training, 554–59 378f, 383f
variation capacity, 629n5
importance of, 328 childhood poverty influencing , 519–20
in insight, 426–27 emotion and, 457–59
learning to vary, 220–33, 527, 583, 597 fluid intelligence and, 375–80, 615n7
motivation and, 229 gestures influencing , 159–60
operant, 228 goals and, 343, 457–58
Royce, Josiah on, 597, 625n10 iCASA framework and, 385–86
useful, 597–98 low capacity of, 318
variety seeking, 278–80, 625n10 prefrontal cortex and, 377
VENs. See von Economo neurons spatial, 458
ventromedial prefrontal cortex (VMPFC) systems enabling , 47
lesions, 361, 432 thinking with senses and, 386
role of, 35f, 439–40, 442, 444, 630n3 three-back task and, 376
verbal analogical thinking, 413–14 training, 543–46, 635n4
verbalization, in avoidance theory of worry, updating, 27–28, 343
68–69, 288 verbal, 458
verbal fluency, 372–73 video games and, 557
verbal processing style, 409 workload pressure, 586–87, 586f
verbal working memory, 458 workplace
video gaming, 554–59 burnout and, 588–89
virtue regrets, 45 creativity in, 212, 219
visual categorization, by monkeys, 344–52, 345f, enrichment of, 496–99
347f–348f interventions, 591–92
visual-spatial analogical problems, 75 neuroendocrinology and, 589–90
visual-spatial planning task, 578 pressure in, 586–87, 586f
visuospatial pattern-completion problems, worry, chronic, 14, 618n8
411–13, 411f abstract memory and, 68–71
VMPFC. See ventromedial prefrontal cortex automatization and, 618n10
I n dex 763