Introduction
It is widely known that sexual dimorphism is an important component of the morphological variation in biological populations (see, e.g., Klein and Cruz-Uribe, 1983; Oxnard, 1987; Kelley, 1993). In higher Primates, sexual dimorphism is also related to some aspects of the social organization and behavior (Alexander et al., 1979; Clutton-Brock, 1985). Thus, it has been observed that the most dimorphic species tend to polygyny and a social organization based on male dominance, whereas in the less dimorphic species, monogamy and family groups are more common. Fleagle et al. (1980) and Kay (1982), on the other hand, have suggested that the behavior of extinct species can be inferred on the basis of sexual dimorphism and, e.g. Plavcan and van Shaick (1992) think that sex differences in size among primate species reflect processes of an ecological and social nature. Some references on sexual dimorphism regarding human populations can be seen in Lovejoy (1981), Borgognini Tarli and Repetto (1986) and Kappelman (1996)!
These biological facts do not appear to be controversial. However, they are based on a series of different sexual dimorphism measures, or indices. Sexual dimorphism, in most works, is measured on the assumption that a random variable is being taken into account. This means that there is a law which accounts for the behavior of the whole set of values that compose the domain of the random variable, a law which is called distribution function. Because both studies of sexual dimorphism aim at establishing differences, in some random variable, between sexes and the behavior of the random variable is accounted for by its distribution function, it seems reasonably clear that a sexual dimorphism study should be equivalent to a study whose main purpose is to determine to what extent the two distribution functions - one per sex - overlap (see shaded area in Fig. 1, where two normal distributions are represented).
Read more about this topic: Sexual Dimorphism Measures
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