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Educability-and-Group-Differences-1973-by-Arthur-Robert-Jensen

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Between-<strong>Group</strong>s Heritability 145<br />

could be accompanied <strong>by</strong> lowered within-group heritabilities. But<br />

the opposite relationship is more likely. It is much like the probabilistic<br />

but not necessary relationship between the number of years<br />

since a person’s birth <strong>and</strong> whether or not he is living or dead. If,<br />

in a city’s birth register, we look up a particular person, John Doe,<br />

<strong>and</strong> know only his birthdate, we can consult a life insurance<br />

company’s actuarial tables <strong>and</strong> determine the probability of living<br />

to the age of John Doe. The probability of living to John Doe’s<br />

age will be some value between 0 <strong>and</strong> 1. But no actuarial probability<br />

tables can help us in establishing that John Doe is in fact living<br />

or dead. The more years that have elapsed since his date of birth,<br />

the greater is the likelihood that we will be right if we assume (i.e.,<br />

hypothesize) that John Doe is dead. We could always be wrong,<br />

but the likelihood of this decreases the greater the time elapsed<br />

since the birth of John Doe. And so it is with the likelihood of<br />

there being a genetic difference between subpopulations; the greater<br />

the heritability of a trait within groups, the greater is the likelihood<br />

that between-group differences in the trait involve genetic factors.<br />

But proof of the genetic hypothesis for any particular trait depends<br />

upon other evidence, just as proof that a particular John Doe is<br />

alive cannot b&proved <strong>by</strong> the actuarial tables. But if John Doe was<br />

born in 1870, how many of us would want to place our bet on the<br />

hypothesis that he is alive today Of essentially the same nature<br />

is our acceptance of the Watusi-Pygmy difference as genetic<br />

without formal proof.<br />

The same thing holds true, though to a lesser degree of likelihood,<br />

in the case of intelligence differences between social classes<br />

<strong>and</strong> racial groups. This valid limitation of generalizing heritability<br />

studies within populations to differences between populations is<br />

vigorously <strong>and</strong> correctly insisted upon <strong>by</strong> some writers (who,<br />

however, usually fail to point out the increasing likelihood<br />

relationship) while at the same time they show no hesitancy<br />

whatever about generalizing environmental sources of variance<br />

from one population to another. Hirsch (1970), for example, cites<br />

a study8 of mid-Eastern Jewish children in Israel brought up in<br />

a kibbutz who had IQs 30 points higher than similar children<br />

brought up in individual homes. Hirsch concludes: ‘There is no<br />

basis for expecting different overall results for any population in<br />

our species’ (Hirsch, 1970, p. 101). How does this differ from<br />

generalizing the heritability of intelligence from, say, Cyril Burt’s

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