Bruce Bagemihl - Biological Exuberance

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Biological Exuberance: краткое содержание, описание и аннотация

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A
Best Book One of the New York Public Library’s “25 Books to Remember” for 1999 Homosexuality in its myriad forms has been scientifically documented in more than 450 species of mammals, birds, reptiles, insects, and other animals worldwide.
is the first comprehensive account of the subject, bringing together accurate, accessible, and nonsensationalized information. Drawing upon a rich body of zoological research spanning more than two centuries, Bruce Bagemihl shows that animals engage in all types of nonreproductive sexual behavior. Sexual and gender expression in the animal world displays exuberant variety, including same-sex courtship, pair-bonding, sex, and co-parenting—even instances of lifelong homosexual bonding in species that do not have lifelong heterosexual bonding.
Part 1, “A Polysexual, Polygendered World,” begins with a survey of homosexuality, transgender, and nonreproductive heterosexuality in animals and then delves into the broader implications of these findings, including a valuable perspective on human diversity. Bagemihl also examines the hidden assumptions behind the way biologists look at natural systems and suggests a fresh perspective based on the synthesis of contemporary scientific insights with traditional knowledge from indigenous cultures.
Part 2, “A Wondrous Bestiary,” profiles more than 190 species in which scientific observers have noted homosexual or transgender behavior. Each profile is a verbal and visual “snapshot” of one or more closely related bird or mammal species, containing all the documentation required to support the author’s often controversial conclusions.
Lavishly illustrated and meticulously researched, filled with fascinating facts and astonishing descriptions of animal behavior,
is a landmark book that will change forever how we look at nature.
[May contain tables!]

Biological Exuberance — читать онлайн бесплатно полную книгу (весь текст) целиком

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60

Vasey “Homosexual Behavior in Primates,” p. 197; for a similar observation, see Wolfe, “Human Evolution and the Sexual Behavior of Female Primates,” p. 130.

61

Hyde, H. M. (1970) The Love That Dared Not Speak Its Name: A Candid History of Homosexuality in Britain, p. 1 (Boston: Little, Brown and Company).

62

Killer Whale (Balcomb et al. 1979:23); published version: Balcomb, K. C., III, J. R. Boran, R. W. Osborne, and N. J. Haenel (1980) “Observations of Killer Whales ( Orcinus orca ) in Greater Puget Sound, State of Washington,” report no. MMC-78/13 to U.S. Marine Mammal Commission, NTIS# PB80-224728. (Washington, D.C.: U.S. Department of Commerce).

63

Musk-ox (Smith 1976; Tener 1965; Reinhardt 1985); Walrus (Miller 1976); Harbor Seal (Johnson 1974, 1976; Johnson and Johnson 1977).

64

Halls, L. K., ed., (1984) White-tailed Deer: Ecology and Management (Harrisburg, Pa.: Stackpole Books); Gerlach, D., S. Atwater, and J. Schnell, eds., (1994) Deer (Mechanicsburg, Pa.: Stackpole Books); Jones, M. L., S. L. Swartz, and S. Leatherwood, eds., (1984) The Gray Whale, Eschrictius robustus (Orlando: Academic Press). In contrast, a similarly comprehensive book on Mule Deer does mention homosexual activity (Geist 1981), as does another volume on White-tailed Deer (Rue 1989).

65

Woodpeckers (Short 1982; Winkler et al. 1995); Skutch, A. F. (1985) Life of the Woodpecker, p. 44 (Santa Monica: Ibis Publishing). For a similar omission of all information on homosexuality in Parrots by the standard “comprehensive” guide to this bird family, see Forshaw (1989).

66

See, for example, Fay (1982) on Walruses, Birkhead (1991) on Magpies, Lowther and Cink (1992) on House Sparrows, Davis (1993) on Black-crowned Night Herons, Lowther (1993) on Brown-headed Cowbirds, Telfair (1994) on Cattle Egrets, Burger (1996) on Laughing Gulls, Russell (1996) on Anna’s Hummingbirds, and Ciaranca et al. (1997) on Mute Swans.

67

Hooded Warbler (Niven 1993:190); Antbirds (Willis 1967, 1972, 1973); Orange-fronted Parakeet (Buchanan 1966); Golden Plover (Nethersole-Thompson and Nethersole-Thompson 1961, 1986); Mallard Duck (Lebret 1961); Black Swan (Braithwaite 1970, 1981); Scottish Crossbill (Nethersole-Thompson 1975); Black-billed Magpie (Baeyens 1981a); Pied Kingfisher (Moynihan 1990). Similar statements have been made by Konrad Lorenz (1991:241 [Greylag Goose]), who claimed that long-term pair-bonding between males only occurs in Geese and Ducks; and Hunt and Hunt (1977:1467 [Western Gull]), who were unaware of any previous reports of homosexual pairing in wild birds.

68

Black-headed Gull (van Rhijn and Groothuis 1985:165; Kharitonov and Zubakin 1984); Adelie Penguin (Davis et al. 1998:136); Humboldt Penguin (Scholten 1992:8); Kestrel (Olsen 452). Similar statements have been issued by scientists studying other species—Sylvestre (1985:64), for example, reported not being aware of any previous records of homosexual activity in Botos, even though fairly extensive descriptions were available in Layne and Caldwell (1964), Caldwell et al. (1966), Spotte (1967), and Pilleri et al. (1980). Walther (1990:308) claimed that courtship betweeen male hoofed mammals had not been observed in the wild, when in fact such behavior had been reported in numerous prior studies, including in Pronghorn, Blackbuck, Mountain Sheep (Bighorn, Thinhorn, Asiatic Mouflon), Mountain Goats, Musk-oxen, Bharal, and Markhor (Walther, F. R. [1990] “Bovids: Introduction,” in Grzimek’s Encyclopedia of Mammals , vol. 5, pp. 290—324 [New York: McGraw-Hill]).

69

See, for example, Takahata et al. (1996:149), who ask, “Is GG-rubbing a sexual behavior?” and conclude that its “nonsexual” aspects are more prominent, because of its association with tension reduction, feeding, reassurance, participation by nonestrous females, and the fact that Bonobos (unlike Japanese Macaques) do not form “exclusive homosexual female-female pairs.” None of these characteristics, in fact, negate a fully “sexual” interpretation. In particular, the fact that Bonobos do not form same-sex pairs or consortships hardly argues against the sexual nature of their genital rubbing—it simply indicates that homosexual interactions in this species do not involve extensive pair-bonding. By these criteria, Bonobo heterosexual interactions would have to be considered nonsexual as well, since they are often associated with the same “social” or “nonsexual” situations, nor do individuals form “exclusive heterosexual male-female pairs.” See also Kuroda (1980:190), who considers genital rubbing between females to be “uninterpretable” when it occurs in contexts that are not related to tension reduction or food exchange; and Kano (1980:253—54, 1992:139,1990:66—67, 69), who classifies same-sex activities in Bonobos as primarily “social” rather than “sexual” and ascribes to them the primary “functions” of greeting, reassurance, reconciliation, and food-sharing (while nevertheless recognizing that sexual aspects may be secondarily involved in some cases). As recently as 1997, researchers were still speculating about, and emphasizing, the nonsexual “functions” of Bonobo homosexual activity (Hohmann and Fruth 1997).

70

Mountain Sheep (Geist 1975:97—98).

71

Vasey, P. L. (1997, August 19) “Summary: Homosexual or Dominance Behavior? (Discussion),” message posted to Primate Talk (on-line discussion list).

72

Rhesus Macaque (Hamilton 1914). A standard and widely cited exposition of the dominance interpretation is Wickler, W. (1967) “Socio-sexual Signals and Their Intra-specific Imitation Among Primates,” in D. Morris, ed., Primate Ethology, pp. 69-147 (London: Weidenfield and Nicolson).

73

On the occurrence of dominance hierarchies in various mammals and birds without homosexuality, and further references, see Wilson, E. O. (1975) Sociobiology: The New Synthesis, p. 283 (Cambridge and London: Belknap Press); Welty, J. C., and L. Baptista (1988) The Life of Birds , 4th ed., pp. 206-210 (New York: W. B. Saunders).

74

For explicit statements on the absence, unimportance, or irrelevance of dominance hierarchies in these species or populations, see Gorilla (Yamagiwa 1987a:25; Robbins 1996:957); Savanna (Olive) Baboon (Rowell 1967b:507-8); Bottlenose Dolphin (Shane et al. 1986:42); Zebras (Penzhorn 1984:113; Schilder 1988:300); Musk-ox (Smith 1976:92-93); Koala (Smith 1980:187); Buff-breasted Sandpiper (Lanctot and Laredo 1992:7); Tree Swallow (Lombardo et al. 1994:556). In Gorilla all-male groups, dominance is not a central organizing feature of social interactions (including homosexual interactions) even though some semblance of a dominance “hierarchy” may exist and males clearly have different ranks. The same may also be true for Hanuman Langur all-male groups (Weber and Vogel 1970:75) and Collared Peccary mixed-sex groups (Sowls 1997:151-53) in which same-sex interactions occur. In Buff-breasted Sandpipers, although mounting between males may be accompanied by aggression and therefore superficially appears related to “dominance,” there is in fact no evidence that a dominance hierarchy exists in this species or constitutes an important aspect of its social organization. In some of these species (e.g., Zebras, Musk-oxen, Bottlenose Dolphins) dominance hierarchies are more prominent in captivity, although homosexual activity occurs in both wild and captive contexts. Finally, J. Steenberg (personal communication) suggests that mounting between female Matschie’s Tree Kangaroos is a dominance display, yet Hutchins et al. (1991:154-56, 161) found no clear-cut dominance hierarchy in the study population where this behavior was observed.

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