Brain Size Matters: a Reply to Peters
by J. Philippe Rushton and C. Davison Ankney
University of Western Ontario
Peters (1993) claimed that published research on brain size and
IQ is flawed because it did not meet his list of minimum
conditions that (a) subjects should be matched for height, weight
and age, (b) analyses should be conducted separately within sex,
(c) subjects should not vary in prenatal and nutritional history,
(d) people with IQs appreciably below the population mean of 100
should not be studied, and (e) brain size measures should be done
blind . However, these conditions have either been met or are
unnecessary and/or inappropriate. We show, contrary to Peters'
claims, that (a) brain size is related to mental abilities, (b)
brain size varies by sex and race, and (c) mental abilities vary
by sex and race. Finally, we suggest that brain size constraints
on behavioural complexity may be best understood from an
evolutionary perspective.
In a reply to Lynn (1993) about brain size and IQ, Peters (1993)
charged bias and questionable motives to dismiss relations first
established over 100 years ago. Peters (1993) claimed that studies of
brain size are confounded by systematic bias, including racial bias ,
over and above normal measurement error. Peters (1993) also
conjectured that uni-directional measurement errors may exist and so
he dismissed Rushton's (1992) analyses showing race and sex
differences in cranial capacity in 6,325 U.S. military personnel.
Consequently, Peters claimed that such studies must be done blind ,
i.e., the person doing the measurement should not know the race of the
subject being measured.
Peters did not note, although it was made clear in Rushton's (1992)
paper, that (1) Rushton neither made the measurements nor knew who
did, and (2) measurements were made to determine proper helmet sizes
not brain sizes (i.e., they were done blind , as the measurers were
unaware of the use that Rushton would make of their data). The East
Asian/European/African differences that Rushton (1992) found in
cranial capacity (cm3) using external head measurements are similar to
those found by Beals, Smith, and Dodd (1984) who estimated cm3 from
endocranial volume, and by Ho, Roessmann, Straumfjord, and Monroe
(1980) who weighed brain mass (grams) at autopsy. Does Peters believe
that Ho et al. leaned on their scales, when weighing brains of
European-Americans, by just enough to produce the same difference
caused by extra snug measurements supposedly made by those measuring
heads of African-Americans? Regardless, it is implausible that the
racial bias alleged by Peters would also produce findings that East
Asians have relatively larger brains than do Europeans.
Peters (1993) misstates when and why it is appropriate to correct for
variation in body size (e.g., height or weight) when analyzing human
attributes. It is only appropriate to correct for body size if one
wishes to determine whether two (or more) individuals or groups are
relatively different in some attribute, when it is already known that
they are absolutely different in that attribute and/or in body size.
For example, men and women differ in both absolute brain size and
absolute body size. Thus, it is appropriate to correct for body size
to determine if men have relatively larger brains. But, it would be
inappropriate to correct for body size to determine if men have
absolutely higher IQs.
Consider this simple analogy: John Doe is 178 cm tall and can jump 1 m
off the ground, whereas basketball star Michael Jordan is 208 cm tall
and can jump 1.17 m off the ground. There are two questions that we
can ask from this: (1) For his size, can Michael Jordan jump higher?
(Answer is no he's 17% taller and can jump 17% higher), and (2) Can
Michael Jordan jump higher? (Answer is, obviously, yes).
Now, consider Peters' argument that to determine if larger brains
produce (absolutely) higher IQs, one must correct for body size. This,
as can be seen from the above, makes no sense. A higher IQ is a higher
IQ (just as a higher jump is a higher jump) regardless of body size.
On average, taller people have higher IQ's, not because they are
taller, per se, but because, on average, they have larger brains.
Correcting for body size reduces the question to a nullity, i.e., do
tall people with their larger brains have relatively higher IQ's?
Peters erred similarly when he argued that age must be controlled when
analyzing brain-size/IQ relations in adults. Both brain size (Ho et
al., 1980) and IQ (Brody, 1992) decline after the age of 45 years.
This likely is not coincidental but, regardless, if one corrects for
age then the result would simply be that brains of similar size tend
to produce similar IQ's.
Peters' erroneously stated that subjects in studies of brain-size/IQ
relations should have similar early-life nutrition and be from the
same social class. His rationale is that these factors can affect
brain size. But, the question is do people with smaller brains have
lower IQ's? , not why do they have smaller brains? . It might be
interesting to know why John Doe is shorter than Michael Jordan but,
regardless, he cannot jump as high.
As Lynn (1993) showed, the IQ/brain-size relation is ubIQuitous.
Studies, additional to those provided by Lynn (1993), show that the
correlation ranges from 0.10 to 0.30 with a mean of about 0.20
(Wickett, Vernon, & Lee, 1994). The head-perimeter/IQ relation occurs
in Orientals as well as whites and blacks and is apparent early in
life. The National Collaborative Perinatal Project (Broman et al.,
1987) found that head perimeter at birth, at 1 year, and at 4 years
correlated with IQ at age 7 from r = 0.13 to 0.24 in 19,000 black and
17,000 white children. Jensen and Johnson (1994) used these data to
show that head size at age 7 (although not at age 4) is correlated
with IQ within-families (i.e., among same-sex full siblings, with age
partialed out), thus indicating a functional relation between brain
size and IQ.
Magnetic resonance imaging technIQues that create a 3-dimensional
model of the brain in vivo confirm the brain-size/IQ relation. Five
studies found an average correlation greater than 0.40, an improvement
over studies that used head perimeter as a measure (Willerman et al.,
1991; Andreasen et al., 1993; Raz et al., 1993; Egan et al., 1994;
Wickett et al., 1994). Peters critIQued the two studies then
available, but only confused the issue. First, he claimed that
Willerman et al.'s (1991) low IQ group, because it averaged only 90.5,
was an improper control . It was, however, not intended to be a
control. Importantly, Willerman et al. showed that those with below
average IQ had, on average, smaller brains. Second, Peters (1993)
almost conceded the brain-size/IQ relation in his footnote citation to
Andreasen et al. (1993). However, even there he suspected bias, i.e.,
self-selection of subjects. But, this could only bias such results if
people with large-brains/high-IQ and small-brains/low-IQ volunteered,
whereas those with large-brains/low-IQ and small- brains/high-IQ did
not. We are unaware of evidence to support such an implausibility.
Regardless, beside studies by Willerman et al. (1991) and Andreasen et
al. (1993) cited by Peters (1993), the brain-size/IQ relation
established using magnetic resonance imaging was corroborated by Raz
et al. (1993), Egan et al. (1994), and Wickett et al. (1994).
The null hypothesis of no relation between brain size and IQ is false.
In anticipation of this, Peters (1993) argued that even if
brain-size/IQ correlations are valid, they account for only a small
percentage of variation. But, it is predictable that correlations
between IQ and overall brain size will be modest. First, much of the
brain is not involved in producing what we call intelligence; thus,
variation in size/mass of that tissue will reduce the correlation.
Second, IQ is an imperfect measure of intelligence and thus, variation
in IQ scores is an imperfect measure of variation in intelligence.
Peters (1993) correctly noted the absolute male/female difference in
brain size. He was, however, incorrect that comparisons of brain size
across sex cannot be made because there are (supposedly) no
appropriate scalars of body size. Ankney (1992) reexamined Ho et al.'s
(1980) autopsy data on 1,261 Americans aged 25 to 80 after excluding
obviously damaged brains. Using allometric technIQues that are
standard in comparative biology, Ankney (1992) found that at any given
surface area or height, brains of European-American men are heavier
than those of European-American women and brains of African-American
men are heavier than those of African-American women. For example,
among 168 cm (5'7 ) tall European-Americans (the approximate overall
mean height for men and women combined), brain mass of men averages
about 100 grams heavier than that of women.
Ankney's (1992) results were confirmed in Rushton's (1992) study of a
stratified random sample of U.S. Army personnel. After adjusting for
effects of age, stature, weight, military rank and race, cranial
capacity of men averaged 1,442 cm3 and women 1,332 cm3. This
difference was found in all of the many analyses that were done to
control for various possible body size effects (see Rushton, 1992).
Moreover, the difference was replicated across samples of
Asian-Americans, European-Americans and African-Americans, as well as
in officers and enlisted personnel.
Peters (1993) correctly noted the paradox that women have
proportionately smaller brains than do men, but apparently have the
same IQ scores. Thus, Ankney (1992) proposed that the sex difference
in brain size relates to those intellectual abilities at which men
excel. Briefly, according to Kimura (1992), women excel in verbal
ability, perceptual speed, and motor coordination within personal
space; men do better on various spatial tests and on tests of
mathematical reasoning. Ankney hypothesized that it may require more
brain tissue to process spatial information. Just as increasing word
processing power in a computer may require extra capacity, increasing
3-dimensional processing, as in graphics, requires a major jump in
capacity. In support of Ankney's hypothesis, although Lynn (1994)
found that men average 4 points higher than do women on standard IQ
tests, Ankney (1995) showed that nearly all of this difference derived
from men's higher scores on spatial and mathematical reasoning
subtests.
Rushton (1995) reviewed 100 years of scientific literature and found
that across a triangulation of procedures, brains of East-Asians and
their descendants average about 17 cm3 (1 in3) larger than those of
Europeans and their descendents whose brains average about 80 cm3 (5
in3) larger than those of Africans and their descendents. Although
critics can pick outliers to show counter-examples and suggest
opposite trends (as could critics of a statement that men are, on
average, taller than women) the aggregated data are clear (see
Rushton, 1995, for full discussion of alleged counter examples).
Consider the following statistically significant comparisons. Using
brain mass at autopsy, Ho et al. (1980) summarized data for 1,261
adults (see above) and reported a sex-combined difference between 811
European- Americans with a mean of 1,323 g (sd = 146) and 450
African-Americans with a mean of 1,223 g (sd = 144). Using endocranial
volume, Beals et al. (1984, page 307, Table 5) analyzed 20,000 crania
and found sex-combined brain cases differed by continental area.
Excluding Caucasoid areas of Asia (e.g., India) and Africa (e.g.,
Egypt), 19 East Asian populations averaged 1,415 cm3 (sd = 51), 10
European groups averaged 1,362 cm3 (sd = 35) and 9 African groups
averaged 1,268 cm3 (sd = 85). Using external head measure- ments,
Rushton (1992) found, in a stratified random sample of 6,325 U.S. Army
personnel, measured in 1988 to determine head size for fitting
helmets, Asian-Americans, European-Americans, and African-Americans
averaged 1,416, 1,380, and 1,359 cm3, respectively (see also, Rushton,
1994).
Globally, racial differences in brain size parallel those found in
measured intelligence. Europeans in North America, Europe and
Australasia have mean IQs of around 100. For East Asians, measured in
North America and in Pacific Rim countries, means range from 101 to
111. Africans living south of the Sahara, African-Americans and
African-Caribbeans (including those living in Britain), have mean IQs
of from 70 to 90 (Lynn, 1991). Elementary speed of information
processing in 9- to 12-year-olds, in which children decide which of
several lights stands out from others, show that racial differences in
mental ability are pervasive. All children can perform the tasks in
less than 1 s, but more intelligent children, as measured by
traditional IQ tests, perform the tasks faster than do less
intelligent children. Japanese and Hong Kong children have faster
decision times (controlling for movement time) than do British and
Irish children who have faster decision time than South African Black
and African-American children (Jensen, 1993; Jensen & Whang, 1993;
Lynn, 1991).
Metabolically, the human brain is an expensive organ. Representing
only 2% of body mass, the brain uses about 5% of basal metabolic rate
in rats, cats, and dogs, about 10% in rhesus monkeys and other
primates, and about 20% in humans. Thus, from an adaptationist
perspective, unless large brains substantially contributed to
evolutionary fitness (defined as increased survival of genes through
successive generations), they would not have evolved.
Paradoxically, Peters (1993) cited Haug (1987) to refute speculations
about the significance of differences in brain size across
individuals, sex, or race , even though Haug (1987, p.135) reported a
correlation of r = 0.479 (n = 81, p < .001) between number of cortical
neurons and brain size including both men and women in the sample.
Haug's analysis showed that a person with a brain size of 1,400 cm3
has, on average, 600 million fewer cortical neurons than an individual
with a brain size of 1,500 cm3. The difference between the low end of
normal (1,000 cm3) and the high end (1,700 cm3) equates to 4.200
billion neurons (a difference of 27% more neurons for a 41% increase
in brain size).
Haug noted that most female data points lay above the regression line
(i.e., women average more neurons for a given brain size than do men).
This suggests that women's brains are differently organized than are
men's, and so causes and results of race differences in brain size may
be different from those of sex differences. Kolakowski and Malina
(1974) hypothesized that differing roles of men and women during human
evolution produced a sexual dichotomy in abilities. Men roamed from
the home base to hunt, which would select for targeting ability and
navigational skills; women were relatively sedentary. Ankney (1992,
1995) expanded on this hypothesis to argue that selection for such
abilities also selected for relatively larger brains in men and that
it may require more brain tissue to process spatial information.
Rushton (1995) provided an evolutionary hypothesis for why East Asians
have the largest brains. The currently accepted view of human origins
posits a beginning in Africa some 200,000 years ago, an
African/non-African split about 110,000 years ago, and a European/East
Asian split about 40,000 years ago (Stringer & Andrews, 1988).
Evolutionary selection pressures were different in the hot savanna
where Africans evolved than in the cold arctic where East Asians
evolved. According to Rushton (1995), the further north the
populations migrated, out of Africa, the more they encountered
cognitively demanding problems of gathering and storing food, gaining
shelter, making clothes, and raising children during prolonged
winters. As the original African populations evolved into Europeans
and East Asians, they did so in the direction of larger brains,
greater intelligence, slower rates of maturation, and other traits
that differentiate these populations.
The evidence is overwhelming that there are racial and sexual
differences in brain size, that there are racial differences in
general IQ, that there are sexual differences in verbal versus
performance IQ, and that differences in mental abilities are related
to differences in brain size. Peters cannot simply deny this evidence.
Thus, important research questions include (1) what is responsible for
the group differences, i.e., are they genetically and/or
environmentally caused?, (2) does the brain size/IQ correlation
indicate cause and effect ?, and (3) is there bidirectional causality
such that the greater learning ability of high IQ children feeds back
to produce even larger brain size?
Address correspondence to:
rushton@sscl.uwo.ca
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