Studying Human Biological Diversity 289
environment. Clinal analysis of a continuous trait such as
body shape, which is controlled by a series of genes, al-
lows anthropologists to interpret human global variation
in body build as an adaptation to climate.
Generally, people long native to regions with cold cli-
mates tend to have greater body bulk (not to be equated
with fat) relative to their extremities (arms and legs) than do
people native to regions with hot climates, who tend to be
relatively long and slender. Interestingly, these differences
show up as early as the time of Homo erectus, as described
in Chapter 8. A person with larger body bulk and relatively
shorter extremities may suffer more from summer heat
than someone whose extremities are relatively long and
whose body is slender. But they do conserve needed body
heat under cold conditions. A bulky body tends to conserve
more heat than a less bulky one, because it has less surface
area relative to volume. In hot, open country, by contrast,
people benefit from a long slender body that can get rid of
excess heat quickly. A small slender body can also promote
heat loss due to a high surface area-to-volume ratio.
In addition to very long-term effects that climate
may have imposed on human variation, climate can also
genes become more common in subsequent generations.
Similarly, the polymorphism of the human species has
allowed us to thrive in a wide variety of environments.
When polymorphisms of a species are distributed into
geographically dispersed populations, biologists describe
this species as polytypic (“many types”); that is, genetic
variability is unevenly distributed among populations. For
example, in the distribution of the polymorphism for blood
type (four distinct phenotypic groups: A, B, O, or AB), the
human species is polytypic. The frequency of the O allele is
highest in American Indians, especially among some popu-
lations native to South America; the highest frequencies of
the allele for type A blood tend to be found among certain
European populations (although the highest frequency is
found among the Blackfoot Indians of the northern Plains
in North America); the highest frequencies of the B allele are
found in some Asian populations (Figure 12.1). Even though
single traits may be grouped within specific geographic
regions, when a greater number of traits are considered,
specific human “types” cannot be identified. Instead each of
these traits is independently subject to evolutionary forces.
As mentioned above, today anthropologists study
biological diversity in terms of clines, or the continuous
gradation over space in the form or frequency of a trait.
As mentioned in Chapter 2, the spatial distribution or
cline for the sickle-cell allele allowed anthropologists to
identify the adaptive function of this gene in a malarial
polytypic Describing the expression of genetic variants in dif-
ferent frequencies in different populations of a species.
Eskimos
Blackfoot
Indians
Chippewa
Indians Whites
(Michigan)
Blacks
(New York)
Bushmen
BO
A
World distribution of the A, B, O
gene frequency (selected studies)
Ghanans
Nigerians
Nilotes
Basques Swiss
English
Russians
Chinese
Japanese
Bengalis
Thai
Papuas SolomonIslanders
Cape York
Aborigines
Australian
Aborigines
Icelanders
Saami
Navaho
Indians
Maya
Indians
Pemon
Indians
Makiritare
Indians
Xavante
Indians
Mapuche
Indians
Aleuts
Figure 12.1 Frequencies of the three alleles for the A, B, and O blood groups for selected
populations around the world illustrate the polytypic nature of Homo sapiens. The frequency of
the alleles differs among populations.