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BF 02477272
BF 02477272
MATHEMATICAL BIOPHYSICS
VOLUMe.27, 1965
SPECIAL ISSUE
D E V E L O P M E N T OF S T R U C T U R E I N A S O C I E T Y W I T H A
DOMINANCE RELATION WHEN NEW MEMBERS ARE
ADDED SUCCESSIVELY
• H. G. I ~ D A U
Committee on Mathematical Biology,
The University of Chicago
cl ~ c2 > - . . - ~ c~ (2)
where in (2) each member is dominated by all the preceding members and
dominates all those t h a t follow. For the hierarchy, h = 1, and for equality,
when all the vt are equal (which is exactly possible only for n odd), h = 0.
The statistical theory of the method of paired comparisons is concerned with
preferences between pairs of objects. The preference relation corresponds
exactly to our dominance relation so that some of the mathematical theory
coincides. Various measures of departure from strict ranking of the objects
have been considered for paired comparisons, such as the number of circular
triads and the coe~cient of consistence defined by M. G. Kendall and B. Babing-
ton Smith (1940). As shown by H. A. David (1963), these are linear functions
of ~ = 1 (vt - ~)2 and thus essentially equivalent, and equivalent to h.
I n I, we considered the structure of a society as resulting essentially from a
round-robin tournament, with the probabilities for the direction of dominance
between each pair of members being determined by inherent characteristics of
the members. I t was shown that ff the members were selected at random from
a homogeneous population, then the value of h would be expected to be near
zero unless small differences in the characteristics were decisive for determining
dominance. However, in the observations on small (n = 10 to 20) flocks of
hens, which were the originM impetus to these investigations, values of h near
one were generally obtained.
I n II, the structure was considered to have been established by some
unspecified process and then to undergo possible change as the result of repeated
contests between members. The outcome of each contest, i.e., direction of
dominance, was considered to be due to social factors, essentially the relative
scores of the members involved. I t was concluded that these social factors
could account for values of h near one, especially with n not too large.
I n this paper we consider another possible mode of development of the
structure, which was mentioned in II. We consider what happens when a
new member is introduced into a society with an established structure, and
thus build up our society by successively adding new members. When a
new member is added, he is considered to engage in a contest with each of the
ANIMAL SOCIETY STRUCTURE 153
which is the score of the new member, is determined by the scores of the older
members.
Writing h~+ 1 for h(V.+ 1), then
12
h.+l=M.+l ~ v~- , where Mn+l (6)
t=l n(n + l)(n + 2)"
Now putting
$
w,=v~-~., m=v~-v~-½, (7)
then
= 2 + 2 + [2 (8)
where ~. indicates summation over i = 1 to n.
We can now compute the expected value of h n + 1. TMs is the conditional
expectation, given Vn+l, i.e., E(hn+ 1 I Vn). We need
h~
w2 = ~ where h~ = h(V~), (9)
and
~+~(2pc-1)(2pj-l) (12)
where we h a v e used E ( ~ ) = ¼ a n d
by E(h.+: I h.). This would not be true in general if the Pt were more
complicated than a linear function of the yr.
3. Difference Equation for Expected Value of h. We can write (17) as
E(h.+: I It.) = A.h. + B. (18)
with
& - 1 [1 + r. (19)
=n - 4]'
3
Bn = [2 + (n - 1)(a, + r,fi,)2]. (20)
(n + 1)(n + 2)
Suppose we consider our societies as being built up by starting with a
society of two members, and adding a single member at a time. For n = 2,
the only possible value of h2 is one. Then
E(h3 l h2) = A2h2 + B2. (21)
Let hsj be the possible values of the random variable, h3, then
E(h4 [haj) = A3h3j + Ba. (22)
I f we multiply each of these equations by Pr(haj I h2), the probability of haj
given h2, and sum over j, then the right side is AaE(h a I h2) + Ba and the left
side is E(h4 I h2). Continuing this way it is clear that from (18) we have
E(h.+: [ h2) = A.E(h. [ h2) + B., n = 2, 3, 4 , . . . . (23)
This is a recurrence relation, allowing us to determine the expected value of h n
for n > 2, starting with h 2 = 1.
For brevity, let
u. ..= E(h. [h2) (24)
so t h a t (23) is
u,~+l = A . u . + B., n = 2, 3, 4 . . . . (25)
with A . and B . given by (19) and (20), and u2 = 1.
More generally, ff we start with any ha, where h m is the value of h for a
definite Vm, then letting
u..= = E(h. Ibm) (26)
we have the equation
u,+:.m = A,u,.m + B,, for n = m, m + 1 , . . . (27)
with
um. = (28)
A general expression for u.. m satisfying (27) and (28) is readily obtained
using standard methods in the theory of difference equations.
156 H.G. LANDAU
Putting
n
Yn = 1 - I &
]=ra
°
Y n = n ( n + 1)(n + 2) Rn where Rn = h(
k=2
1
giving
u n = n(n2 6_ 1) R n _ 1{ 1 + ~l n~k--~'2
-1 [2 + (k - 1)(a k + rk~k)u]~,
for n = 3, 4 , . . . . (31)
4. Case 1: r n = O. Suppose first t h a t we consider t h a t p,, the probability of
the new m e m b e r being d o m i n a t e d b y older members, is independent of the v,,
the scores of the older members. T h e n rn = 0, a n d R , = 1 for all n, so (31)
becomes
6 { 1+ In-1 }
un = n(n 2 -- 1) ~ ~ k[2 + (k - 1)a~] • (32)
k=2
un+l = n + 2
n-l[ 1
+ - -
n - 1 4(n - 1) 2 un +
3
(41)
(n + 1)(n + 2) + (n -
W e consider only a > 0, because a < 0 would m e a n t h a t the old m e m b e r s
with low scores are more likely to d o m i n a t e the new m e m b e r t h a n are those
158 H.G. LANDAU
with high scores, which seems unrealistic. Now we compare the values o f u~
given b y (41) to those in Case 1 (r n = 0 or a -- 0), with t h e value of b being t h e
same as a in Case 1. E q u a t i n g b to a in Case 1 means t h a t p~ for a m e m b e r
w i t h a n average score, vn, is t h e same in t h e two cases. I t can be seen t h a t (41)
always gives higher values of u n because the f a c t o r
CC O~2
1+
n -- 1 4 ( n -- 1) 2
( ~
0 °
Un+l = 1 n 2 - 1" Un + n + 1
U,~=
n-----~
- [6'1+ k4_ .. , ~ "k J
We then use
~1 ~1- 1
I n n = C + 2n
1
12n 2 + " "
~ 1 . .92. . 1 + 1 ÷...
un = n In + , for a = 2, (44)
is good for n > 6. Direct calculation of ul0 from (41) gives the value 0.811
while (44) gives 0.805.
The value a -- 2 is the largest possible for the linear dependence o f p t on v t.
I t means t h a t the new member is certain to be dominated b y an older one with
a score of n - - 1 and is certain to dominate one with a score of zero, with
intermediate probabilities for the others.
6. Conclusion. The results here are similar to those in II. The increase of
Pt with v~ tends to increase the expected value of h toward one for moderate n.
For large n, u n decreases because of the restrictions on the parameters a and b
imposed by the assumption of linearity. These result in p~ being near its value
for v = vn for most of the c~, i.e., those intermediate between the highest and
lowest ra~king members.
The above results Indicate t h a t un would be still larger ff the dependence of 1~
on v~, instead of being linear, were S-shaped; i.e., Pt near one for most high
ranking c~, near zero for most low ranking c~, and intermediate for others. I f
this type of relation is taken to the extreme, it can be seen to result In the
hierarchy being preserved.
That is, suppose ha = 1, and the c~ are numbered in order of increasing v~, so
160 H.G. LANDAU
v~ = i for i>s+ l,
a n d V,+I is also t h e hierarchy. Thus, once established the h i e r a r c h y would
persist, so t h a t starting w i t h n = 2 as considered above, t h e n h n = 1 for all n
u n d e r this assumption. Here, s could h a v e a n y value in the range 0 to n - 1,
a n d could v a r y with n.
This a s s u m p t i o n simply states t h a t cn+l dominates all c~ below a certain
rank, s, a n d is d o m i n a t e d b y all those a b o v e r a n k s, while the relation to the
sth m e m b e r can be in either direction. I t is then, for t h e hierarchy, a n
a s s u m p t i o n o f t r a n s i t i v i t y o f t h e d o m i n a n c e relation with respect to ca+ 1.
Suppose t h e starting s t r u c t u r e is n o t t h e hierarchy, b u t a similar assumption
still holds for each new m e m b e r , where now the r a n k is m e a s u r e d b y vt a n d can
be t h e same for two or more ce T h e n it can be seen, a l t h o u g h we will n o t write
o u t a p r o o f in detail, t h a t the s t r u c t u r e m u s t change in the direction of t h e
h i e r a r c h y as n increases.
This w o r k was aided b y t h e U n i t e d States Public H e a l t h Service Training
G r a n t No. 5-T1-G/¢I-833 f r o m t h e N a t i o n a l I n s t i t u t e of General l~edical
Sciences.
LITERATURE
David, H.A. 1963. The Method of Paired Comparisons. New York: Hafner Publishing
Co.
Kendall, M. G. and B. B. Smith. 1940. "On the Method of Paired Comparisons."
Biometrika, 31, 324-345.
Landau, H.G. 1951a. "On Dominance Relations and the Structure of Anlmal Societies:
I. Effect of Inherent Characteristics." Bull. Math. Biophysics, 13, 1-19.
1951b. "On Dominance Relations and the Structure of Animal Societies:
II. Some Effects of Possible Social Factors." Ibid., 13, 245-262.