Why Is Sex Fun__ The Evolution of Human Sexuality - Jared M. Diamond [57]
One has to wonder how on Earth animals evolved so that something seemingly so arbitrary as the length of a tail, the color of a spot on a bill, or the width of a black stripe produces such big behavioral responses. Why should a perfectly good Great Tit retreat from food just because it sees another bird with a slightly wider black stripe? What is it about a wide black stripe that implies intimidating strength? One would think that an otherwise inferior Great Tit with a gene for a wide stripe could thereby gain undeserved social status. Why doesn’t such cheating become rampant and destroy the meaning of the signal?
These questions are still unresolved and much debated by zoologists, in part because the answers vary for different signals and different animal species. Let’s consider these questions for body sexual signals—that is, structures on the body of one sex but not the opposite sex of the same species, and that are used as a signal to attract potential mates of the opposite sex or to impress rivals of the same sex. Three competing theories attempt to account for such sexual signals.
The first theory, put forward by the British geneticist Sir Ronald Fisher, is termed Fisher’s runaway selection model. Human females, and females of all other animal species, face the dilemma of selecting a male with which to mate, preferably one bearing good genes that will be passed on to the female’s offspring. That’s a difficult task because, as every woman knows all too well, females have no direct way to assess the quality of a male’s genes. Suppose that a female somehow became genetically programmed to be sexually attracted to males bearing a certain structure that gives the males some slight advantage at surviving compared to other males. Those males with the preferred structure would thereby gain an additional advantage: they would attract more females as mates and hence transmit their genes to more offspring. Females who preferred males with the structure would also gain an advantage: they would transmit the gene for the structure to their sons, who would in turn be preferred by other females.
A runaway process of selection would then ensue, favoring those males with genes for the structure in an exaggerated size and favoring those females with genes for an exaggerated preference for the structure. From generation to generation the structure would grow in size or conspicuousness until it lost its original slight beneficial effect on survival. For instance, a slightly longer tail might be useful for flying, but a peacock’s gigantic tail is surely no use in flying. The evolutionary runaway process would halt only when further exaggeration of the trait would become detrimental for survival.
A second theory, proposed by the Israeli zoologist Amotz Zahavi, notes that many structures functioning as body sexual signals are so big or conspicuous that they must indeed be detrimental to their owner’s survival. For instance, a peacock’s or widowbird’s tail not only doesn’t help the bird survive but actually makes life more difficult. Having a heavy, long, broad tail makes it hard