Gonadal hormones regulate the ability to copulate in most mammalian species
, but not in primates because copulatory ability has been emancipated from
hormonal control. Instead, gonadal hormones primarily influence sexual moti
vation. This separation of mating ability from hormonally modulated mating
interest allows social experience and context to powerfully influence the e
xpression of sexual behavior in nonhuman primates, both developmentally and
in adulthood. For example, male rhesus monkeys mount males and females equ
ally as juveniles, but mount females almost exclusively as adults. Having e
jaculated with a female better predicted this transition to female mounting
partners than did increased pubertal testosterone (T). It is proposed that
increased pubertal T stimulates male sexual motivation, increasing the mal
e's probability of sexual experience with females, ultimately producing a s
exual preference for females. Eliminating T in adulthood reduces male sexua
l motivation in both humans and rhesus monkeys, but does not eliminate the
capacity to engage in sex. In male rhesus monkeys the effects of reduced an
drogens on sexual behavior vary with social status and sexual experience. H
uman sexual behavior also varies with hormonal state, social context, and c
ultural conventions. Ovarian hormones influence female sexual desire, but t
he specific sexual behaviors engaged in are affected by perceived pregnancy
risk, suggesting that cognition plays an important role in human sexual be
havior. How the physical capacity to mate became emancipated from hormonal
regulation in primates is not understood. This emancipation, however, incre
ases the importance of motivational systems and results in primate sexual b
ehavior being strongly influenced by social context. (C) 2001 Academic Pres
s.