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CONTENTS VII
GI。目arγ475
References 483
C redits 508
Index 513
is• 0 × cer s
CHAPTER 1
A People云 His切ry ofthe United St,αtes: 1492-Present, Howard Zinn, p. 4
CHAPTER 2
How the Irish Beeαme White, Noel Ignatiev, p. 36
CHAPTER 3
The Persistence ofthe Color Line: Rαcial Politics αnd the Obαmα
Presidency, Randall Kennedy, p. 64
CHAPTER 4
Muslim Girl: A Coming ojAge, Amani Al-Khatahtbeh, p. 96
CHAPTER 5
We Gon' Be Alright: Notes on Rαce αnd Resegreg1αtion, Jeff Chang, p. 128
CHAPTER 6
Bone Black: Memories ofGirlhood, bell hooks, p. 158
CHAPTER 7
How Did 而u Get to Be Mexican? A White/Brown Ma价 Search for
Identity, Kevin Johnson, p. 186
CHAPTER 8
Sαuαgelnequαlities: Children in Americα云 Schools, Jonathan Kozol, p. 218
CHAPTER 9
Divided: The Perils ofOur Growing Inequαli切, David Cay Johnston, p. 248
CHAPTER 10
The Color ofU切lth: The Story Behind the U.S. RαcialU切lthDivide,
Meizhu Lui, Barbara Robles, Betsy Leondar-Wright, Rose Brewer, and
Rebecca Adamson, p. 282
CHAPTER 11
The New Jim Crow: Mαsslncαrcer,αtion 仇 the Age ofColorblindness,
Michelle Alexander, p. 310
XVII
...
XVIII LIST OF EXCERPTS
CHAPTER 12
Fatal Invention: How Science, Politics, a:乱d Big Business Re-Create Race
in the Twenty-First Century, Dorothy Roberts, p. 344
CHAPTER 13
“ Til
Law Do Us Part: Immigration Policy and Mixed-Status Family
Separation,” Ruth Gomberg-Mufi.oz, p. 374
CHAPTER 14
Facebook post, Michelle Alexander, p. 414
CHAPTER 15
Coal to Cream: A Black Man's Jour’n ey Beyond Color to anA.ffirmation of
Rαce, Eugene Robinson, p. 442
OU e u or
XIX
rerace
FEATURES
Race and Racisms includes several unique features designed to aid both teach-
ing and learning. Each of the following features appears throughout the book:
xx
PREFACE XXI
咀1e goal for the second edition of Race and Racisms was not merely to keep up
with our changing world but to invite students to consider their own role in it.
Each chapter has been carefully updated to reflect current issues and events
as well as the latest data and research. Beyond these updates, new stories and
examples throughout engage readers in thinking about how racism could be
addressed or alleviated. Highlights of this edition include:
• Expanded coverage of Arab and Middle Eastern Americans, in addition
to new topics such as Islamophobia.
• The chapter on theory is now introduced earlier in the text (Chapter 4) to
provide a framework for material that follows.
• New Voices or Research Focus sidebars in every chapter.
• New features: At a Glance infographics, Check Your Understanding
summaries, and Talking about Race guidelines and prompts.
Following this preface, we include an overview for the new Talking about
Race feature. We hope this overview, Talking About Race Outside the
Classroom, will serve as a practical guide on how to have thoughtful, informed,
rational discussions about race and racism. ’These are sensitive and emotional
topics that many people have difficulty approaching. 咀1is overview encour-
ages students to engage in constructive conversations about race and provides
tips for countering racist ideology. At the end of each chapter, a brief Talking
about Race section provides some more specific suggestions for approaching
these conversations.
8 Educational Inequality
• Newinfog即hie on educational disparities and life-course effects (p. 229)
New Research Focus box: The Asian American Achievement Paradox
(p. 242)
。 RGANIZATI 。 N
Race and Racisms is divided into three sections, each using an intersectional
framework and global considerations to guide our understanding of racial
dynamics in the United States:
ANCILLARIES
Oxford University Press is proud to offer a complete supplements package to
accompany Race and Racisms: A Critical Approach.
The Ancillary Resource Center (ARC) at www.oup” arc.com is a co盯e
nient, instructor-focused single destination for resources to accompany this
book. Accessed online through individual user accounts, the ARC provides
instructors with up-to-date ancillaries while guaranteeing the security of
grade-significant resources. In addition, it allows OUP to keep instructors
informed when new content becomes available.
Another random document with
no related content on Scribd:
Fig. 41.—Spawn of a
species of Natica
(from a specimen in
the British Museum) ×
½.
(After Souleyet.)
Fig. 50.—Generative and other organs
of Littorina obtusata L., male.
A, anus.
Br, branchia.
H, heart.
I, intestine.
Li, liver.
M, muscle of attachment.
Pe, penis.
Te, testis.
VD, vas deferens.
(After Souleyet.)
Dioecious Mollusca.—The common Littorina obtusata will serve
as a typical instance of a dioecious prosobranchiate, exhibiting the
simplest form of organs. In the female the ovary, a lobe-shaped
body, is embedded in the liver. An oviduct with many convolutions
conveys the ova into the uterus, an oblong chamber which consists
simply of a dilatation of the oviduct. The ova descend into the uterus,
which is sometimes furnished with a seminal pouch. In this seminal
pouch, or above it, in the oviduct, the ova come into contact with the
spermatozoa. The lower part of the uterus secretes a gelatinous
medium (or capsule, as the case may be) in which the fertilised ova
become enclosed previous to exclusion. In position the oviduct abuts
on the kidney, while the uterus is in close proximity to the rectum,
and the female external orifice is found close to the anus, within the
branchial cavity.
The male organs of Littorina are more simple. The testis is
lodged, like the ovary, in the liver; the vas deferens is, like the
oviduct, convoluted, and eventually traverses the right side of the
neck, emerging near the right tentacle, and terminating in the penis
or external copulative organ (Fig. 50).
This system prevails, with but slight modifications in detail,
throughout the prosobranchiate Gasteropoda. The most important
modification is the passage of the seminal products in certain cases
(many of the Diotocardia) through the right kidney, with which the
oviduct and vas deferens always stand in close relation. The same
arrangement occurs in the Scaphoda and some Pelecypoda.
The penis varies greatly in form and size. In the Strombidae (see
Fig. 99) and Buccinidae (Fig. 62) it is very large and prominent; in
Littorina it is somewhat spinulose at one side; in Paludina a portion
of it is lodged in the right tentacle, which becomes atrophied and
much more obtuse than the tentacle on the left side.
Spermatozoa.—The shape of the spermatozoa and of the ova in
Mollusca is of the usual type. In Paludina Ampullaria, and certain
species of Murex two types of spermatozoa occur, one hair-like, the
other worm-like, three times as long as the former, and not tapering
at one end. The former type alone take part in fertilisation, and
penetrate the ovum. It has been suggested that these worm-like
spermatozoa are a kind of incipient ova, and indicate a possible
stage in commencing hermaphroditism. And, since the nearest allies
of the Prosobranchiata (in which these types occur) are
hermaphrodite (i.e. the Opisthobranchiata and Pulmonata), it is not
unreasonable to suppose that the Prosobranchiata should show
some tendency towards hermaphroditism in their genital glands.[256]
Cephalopoda.—The special characteristic of the reproductive
organs in female Cephalopoda is the development of various glands,
some of considerable size, in connexion with the ovary and oviduct.
Sepia, Loligo, and Sepiola are furnished with two large nidamental
glands, which open into the mantle cavity independently of the
oviduct. Their purpose is to produce a viscid mucus, which envelops
the ova at the moment of their emission and eventually hardens into
the egg-capsules. A pair of accessory nidamental glands occur in
Sepia, as well as a pair of smaller glands situated on the oviduct
itself.
In many of the male Cephalopoda the vas deferens is long and
dilated at its outer end into a glandular reservoir, within which are
formed the spermatophores, or narrow cylindrical packets which
contain a very large number of spermatozoa. When charged, the
spermatophores pass into what is known as Needham’s sac, where
they remain until required for use. These spermatophores are a very
characteristic part of the reproductive arrangements in the
Cephalopoda. The male of Sepia has been noticed to deposit them,
during union, upon the buccal membrane of the female. During the
emission of the ova by the female, the spermatophores, apparently
through the agency of a kind of spring contained at one end, burst,
and scatter the spermatozoa over the ova.
The Hectocotylus Arm.—Perhaps the most remarkable feature
in the sexual relations of all the Mollusca is the so-called
hectocotylus of the Cephalopoda. In the great majority of the male
Cephalopoda, one of the ‘arms,’ which is modified for the purpose in
various ways and to a greater or less extent, becomes charged with
spermatophores, and sometimes, during union, becomes detached
and remains within the mantle of the female, preserving for some
considerable time its power of movement.
The hectocotylus is confined to the dibranchiate Cephalopoda,
and its typical form, i.e. when part of the arm becomes disengaged
and left with the female, occurs only in three genera of the
Octopodidae, viz.[Argonauta, Ocythoe (Philonexis), and
Tremoctopus. In all of these, the male is many sizes smaller than the
female. In Argonauta the third arm on the left side becomes
hectocotylised. At first it is entirely enveloped in a kind of cyst, in
such a way that only a small portion of the tip projects; subsequently
the cyst parts asunder, and allows the arm to become expanded to
its full length, which considerably exceeds that of the other arms. At
a certain point the acetabula or suckers terminate, and the
remainder of the arm consists of a very long, tapering, sometimes
thread-like filament, which is pointed at the extreme tip. It is not yet
known how the spermatophores find their way into the hectocotylus,
or how the hectocotylus impregnates the ova of the female. The arm
thus affected is not always the same. In Tremoctopus it is the third of
the right side, in the Decapoda the modification usually affects the
fourth of the left.
Fig. 51.—Male of Ocythoe
tuberculata Raf. (= Philonexis
catenulatus Fér.),
Mediterranean, showing three
stages, A, B, and C, in the
development of the hectocotylus
arm: h.cy, hectocotylus still in
the cyst; c´y´, spoon-shaped cyst
at the end of the arm when
freed; th, thread-like organ freed
by the rupture of c´y´. Natural
size. From specimens in the
British Museum.
This singular property of the male Cephalopoda has only recently
been satisfactorily explained. It is true that Aristotle, more than
twenty-two centuries ago, distinctly stated that certain of the arms
were modified for sexual purposes. Speaking of what he calls the
polypus (which appears to represent the Octopus vulgaris of the
Mediterranean), he says: ‘It differs from the female in having what
the fishermen call the white sexual organ on its arm;’ again, ‘Some
say that the male has something of a sexual nature (αὶδοιῶδές τι) on
one of its arms, that on which the largest suckers occur; that this is a
kind of muscular appendage attached to the middle of the arm, and
that it is entirely introduced within the funnel of the female’.
Unfortunately the word translated by introduced is corrupt, and can
only be restored conjecturally. He again remarks, ‘The last of the
arms, which tapers to a fine point and is the only whitish arm, it uses
in sexual union.’[257]
The typical hectocotylus seems to have entirely escaped notice
until early in the present century, when both Delle Chiaje and Cuvier
described it, as detected within the female, as a parasite, the latter
under the name of Hectocotylus octopodis. Kölliker, in 1845–49,
regarded the Hectocotylus of Tremoctopus as the entire male
animal, and went so far as to discern in it an intestine, heart, and
reproductive system. It was not until 1851 that the investigations of
Vérany and Filippi confirmed a suggestion of Dujardin,[258] while H.
Müller, in 1853, completed the discovery by describing the entire
male of Argonauta.
In all genera of dibranchiate Cephalopoda except Argonauta,
Ocythoe, and Tremoctopus, one of the arms is sexually modified in
various ways, but never becomes so much prolonged, and is never
detached and left with the female. In Loligo Forbesii Stp. the fourth
arm on the left has 23 pairs of regularly developed acetabula, which
then lessen in size and disappear, being replaced by long
pedunculated papillae, of which there are about 40 pairs. In Loligo
vulgaris Lam. and L. Pleii Orb. 18 or 19 pairs of acetabula are
regularly formed, and then occur 40 pairs of papillae, as in Forbesii.
In other species of Loligo (gahi Orb., brevis Bl., brasiliensis Orb.)
only the outer row of suckers becomes modified into papillae after
about the 20th to the 22nd pair. In Sepioteuthis sepioides the
modification is the same as in the Loligo last mentioned, but the
corresponding arm on the right side is so covered with acetabula
towards its extreme end, that it is thought that it in some way co-
operates with the hectocotylised left arm.
In Octopus, the third arm on the right side is subject to
modification. This arm is always shorter than the corresponding arm
on the other side, and carries fewer suckers, but is furnished at the
extreme tip with a peculiar kind of plate, which connects with the
membrane at the base of the arm by a channel of skin, which
probably conveys the spermatophores up to the tip.
In Octopus vulgaris, the species referred to by Aristotle, the
hectocotylised arm is short, thin in its outer half and pointed at the
extremity, while the fold of skin is very white, and gives the arm an
appearance of being divided by a cleft at the side. At the same time,
an unusual development of one or two suckers on the arm is not
uncommon.[259]