Bruce Bagemihl - Biological Exuberance

In other animals the very characteristics that are used to claim that same-sex activities are nonsexual—their briefness, “incompleteness,” or absence of signs of sexual arousal, for example—are as typical, if not more typical, of opposite-sex interactions that are classified as sexual behavior. Nearly a third of all mammals in which same-sex mounting occurs also have “symbolic” or “incomplete” heterosexual mounts in which erection, thrusting, penetration, and/or ejaculation do not occur; “ritual” heterosexual mountings are also typical of many bird species. 109In Kob antelopes, 52 percent of heterosexual copulations involve at least one mount by the male without an erection; in contrast, 56 percent of homosexual mountings between male Giraffes—sometimes classified as nonsexual— do involve erections. Likewise, only one in four to five heterosexual mounts among northern jacanas results in cloacal (genital) contact, and ejaculation probably occurs in less than three-quarters of Orang-utan heterosexual mounts. 110Evidence for sexual arousal or “completed” copulations is often entirely lacking in heterosexual contexts, yet such male-female mounts are still considered “sexual” behavior. In Walruses, Musk-oxen, Bighorn Sheep, Asiatic Mouflons, Grizzly Bears, and Olympic Marmots, for example, penetration and ejaculation are rarely, if ever, directly observable during heterosexual mounts, while male erections are routinely not visible during White-tailed Deer copulations, ejaculation can only be “assumed” to occur in observations of Orang-utan, White-faced Capuchin, and Northern Fur Seal heterosexual mating, and genital contact is difficult to verify during Ruff male-female mounts (among many other species). 111

In fact, actual sperm transfer during heterosexual copulations in many species is so difficult to observe that biologists have had to develop a variety of special “ejaculation-verification” techniques. In birds such as Tree Swallows, for example, tiny glass beads or “microspheres” of various colors are inserted into males’ genital tracts. If the birds ejaculate during a heterosexual mating, these beads are transferred to the female’s genital tract, where they can be retrieved by scientists and checked for their color coding to determine which males have actually transferred sperm. For rodents and small marsupials, biologists actually inject several different radioactive substances into males’ prostate glands. During ejaculation, these are carried via semen into females, who are then monitored with a sort of “sperm Geiger counter” to determine which males, if any, have inseminated them. 112If such elaborate lengths are required to verify a fundamental and purportedly self-evident aspect of heterosexual mating, is it any wonder that homosexual matings should sometimes appear to be “incomplete”?

Because of such difficulties in observation and interpretation, scientists have often employed similarly extreme measures in an attempt to “verify” homosexual intercourse. In the early 1970s, for example, a controversy arose concerning to what extent, if at all, mounting activity between male animals was truly “sexual.” As proof of its “nonsexual” character, some scientists claimed that full anal penetration never occurred in such contexts (thus equating penetration with “genuine” sexuality). Researchers actually went to the trouble of filming captive male Rhesus Macaques mounting each other in order to record examples of anal penetration; they even anesthetized the monkeys afterward to search for the presence of semen in their rectums. Needless to say, the cinematographic proof of anal penetration they obtained did little to quell any subsequent debate about whether such mounts were “sexual”—all it did was institute a revised definition of “sexual” activity. The fact that they were able to document penetration but not ejaculation simply meant that a new “standard” of sexuality could now be applied: only mounts that culminated in ejaculation were to be considered “genuine” sexual behavior. Ironically, none of these researchers were apparently aware of an earlier field report of homosexual activity in Rhesus Macaques in which both anal penetration and ejaculation were observed. 113

This near-obsessive focus on penetration and ejaculation—indeed, on “measuring” various aspects of sexual activity to begin with—reveals a profoundly phallocentric and “goal-oriented” view of sexuality on the part of most biologists. Not just homosexual activity, but noninsertive sexual acts, female sexuality and orgasmic response, oral sex and masturbation, copulation in species (such as birds) where males do not have a penis—any form of sex whatsoever that does not involve penis-vagina penetration falls off the map of such a narrow definition. The fact is that both heterosexual and homosexual activities exist along a continuum with regard to their degree of “sexuality” or “completeness.” Male mammalian mounting behavior, for example, can involve partial mounting, full mounting but no thrusting, thrusting but no erection, erection but no penetration, penetration but no ejaculation, ejaculation but no penetration, penetration and ejaculation without series mounting, and so on and so forth. 114Each stage along this continuum has at one time or another been considered a defining threshold of “true” sexual behavior—often so as to exclude same-sex interactions—rather than as one possible manifestation of a broader sexual capacity that is sometimes, but not always, orgasmically (or genitally) focused.

A nonsexual component of homosexual behavior does appear to be valid in a number of species; in equally many species, there are clear arguments against various nonsexual interpretations, and some zoologists have themselves explicitly refuted nonsexual analyses. 115Overall, though, three important points must be considered in relation to nonsexual interpretations of behaviors between animals of the same sex. First, the question of causality—or the primacy of the nonsexual aspect—must be addressed. Just because an apparently sexual behavior is associated with a nonsexual result or circumstance does not mean that the sole function or context of the behavior is nonsexual. For example, female Japanese Macaques often gain powerful allies by forming homosexual associations, since their consorts typically support them in challenging (or defending themselves against) other individuals. However, a detailed study of partner choices showed that such nonsexual benefits are of secondary importance: females choose their consorts primarily on the basis of sexual attraction rather than on whether they will make the best or most strategic allies. 116Likewise, mounting (or other sexual activity) between animals of the same sex is described in many species (e.g., Bonobos) as a behavior that serves to reduce aggression or tension between the participants. Indeed, individuals who mount each other may be less aggressive to one another or may experience less tension in their mutual interaction, and homosexuality probably does serve a tension-reducing function for at least some animals in some contexts (as does heterosexuality). However, the situation is considerably more involved than this. Tension reduction is as likely to be a consequence of an affiliative or friendly relationship between individuals—a relationship that is also expressed through sexual contact—as it is to be a direct result of their sexual activity. Moreover, as some researchers have pointed out for Bonobos, the causal relationship may also be the reverse of what is usually supposed. That sexual behavior and situations involving tension often co-occur in this species can give the impression that sexuality is functioning only to reduce tension, when in fact it may also create or generate its own tension. Indeed, homosexual activity in male Gorillas often results in increased rather than decreased social tension. 117