Sexual dimorphism
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Sexual dimorphism is the systematic difference in form between individuals of different sex in the same species. Examples include color (specifically referred to as sexual dichromatism), size, and the presence or absence of parts of the body used in courtship displays or fights, such as ornamental feathers, horns, antlers or tusks.
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[edit] Examples
In many species, including most mammals, the male is larger than the female.[1] In others, such as most insects, spiders, reptiles and amphibians, many fish, and certain mammals such as the spotted hyena, the female is larger than the male. Other sex-specific differences include differences in coloration (sexual dichromatism), presence vs. absence of certain body parts (such as horns, antlers, tusks or display feathers), size of the eyes (some insects), possession of stings (various kinds of Hymenoptera), and different thresholds for certain behaviors (aggression, infant care, etc).
Among vertebrates, sexual dimorphism is particularly apparent in ducks and most gamefowl. This is perhaps most dramatic with species of peafowl. Male pheasants are notably larger than females and possess bright plumage, whereas females are usually brown irrespective of the particular species. In some birds, females have brighter colors than males; most of these cases are waders such as the phalaropes and painted snipes. As this is the opposite of the usual sexual dichromatism, it is termed reverse sexual dimorphism. In many predatory birds, females are larger than males, often by a considerable margin. This seems to reduce competition between members of a pair, as they have different optimal prey sizes. Some cases of sexual dimorphism in birds are so striking that males and females of the same species were originally taken to be members of entirely different species, as in the case of the Eclectus Parrot (Eclectus roratus), where the male is predominantly green with an orange beak and the female scarlet and deep blue with a black beak.
The Huia (Heteralocha acutirostris), a New Zealand bird species (now extinct), was another striking example of sexual dimorphism. The male's bill was short, sharp and stout, while the female's was long, thin and crescent-shaped. This beak dimorphism allowed mated pairs of Huia to avoid competing for the same food source, with males chiseling into and breaking apart rotting logs, while females were adept at probing into fresher wood for grubs.
Certain cases of sexual dimorphism have obvious utility beyond mate attraction. An example of this is the Blue Wildebeest (and many other biungulates). The horns of the male are much larger, allowing the male to engage in combat more effectively as he competes with other bucks for mating privileges.
An extreme example of sexual dimorphism is found in the genus Osedax of polychaete worms, which lives on whale falls. The females feed on the bones of the dead whale; the males live inside the females and do not develop past their larval stage, except to produce large amounts of sperm. In the echiuran Bonellia viridis, exposure to adult females causes larvae to develop into tiny, semi-parasitic males which are swallowed and live inside the female's genital sac. In the parasitic barnacles Sacculina, the males are tiny, free-ranging animals, whereas the females only exist as a web-like tissue inside their hosts. In the majority of scale insects, females are highly modified (eyeless and wingless, with non-functional appendages and reduced segmentation), attached permanently to their host plants, while males are rather ordinary though delicate insects, smaller and winged.
Some species of anglerfish also display extreme sexual dimorphism. Females are typical anglerfish, while males are tiny rudimentary creatures with no digestive systems. A male must find a female and fuse with her: he then lives parasitically, becoming little more than a sperm-producing body. A similar situation is found in the Zeus water bug Phoreticovelia disparata where the female has a glandular area on her back that can serve to feed a male that clings to her (note that although males can survive away from females, they generally are not free-living).[2]
[edit] Psychological and behavioral differentiation
Sex steroid-induced differentiation of adult reproductive and other behavior has been demonstrated experimentally in many animals. In some mammals, adult sex-dimorphic reproductive behavior (e.g., mounting or receptive lordosis) can be shifted to that of the other sex by supplementation or deprivation of androgens in fetal life or early infancy, even if adult levels are normal.
[edit] Evolution of sexual dimorphism
[edit] Handicap principle
The handicap principle is the proposed evolutionary force that gives males of some species traits that at first glance seem to place the organism at a disadvantage.
For example, the bright colouration of male game birds makes them highly visible targets for predators, while the drab females are better camouflaged. Other examples are bird of paradise and lyrebird, whose males have such large plumes that their flight is inhibited. Strong smells, loud cries and singing can also attract predators.
The answer that has been suggested to this apparent paradox is that, at a biological level, the reproductive success of an organism is often more important than duration of life. This is particularly apparent in the case of game birds: a male Common Pheasant in the wild often lives no more than 10 months, with females living twice as long. However, a male pheasant's ability to reproduce depends not on how long he lives but whether females will select him to be their mate. A brightly coloured and heavily plumed male presumably demonstrates to the female that he is fit in evolutionary terms—he has been able to survive in spite of impediments and must therefore be a good choice to father her chicks. This explanation was first proposed by Amotz Zahavi.
Development of such characters could not at first be explained in terms of simple natural selection. In 1871 Charles Darwin advanced the theory of sexual selection, which related sexual dimorphism with sexual selection.
[edit] Polyamory
Comparison of sexual dimorphism in birds and their mating habits shows that the time spent in search for mates, staking territories and mating competes with the demands of taking care of young. For birds and in general, it can be stated that the stronger the dimorphism in a species, the more likely is it to be polyamorous and the less is the task of caring for offspring shared among the sexes. This theory is developed by R. L. Trivers' in the parental investment theory. It applies to all ecology.
[edit] Sexual dimorphism in humans
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Top: Stylised illustration of humans on the Pioneer plaque, showing both male (left) and female (right). |
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Sexual dimorphism in humans is the subject of much controversy, especially relating to mental ability and psychological gender. (For a discussion, see biology of gender, sex and intelligence, gender, and transgender.) Obvious differences between men and women include all the features related to reproductive role, notably the endocrine (hormonal) systems and their physiological and behavioural effects. Such undisputed sexual dimorphism include gonadal differentiation, internal genital differentiation, external genital differentiation, breast differentiation, muscle mass differentiation, and hair differentiation.
Externally, the most sexually dimorphic portions of the body are the chest, the lower half of the face, and the entire area between the waist and the knees. [3]
The basal metabolic rate is about 6 percent higher in adolescent boys than girls and increases to about 10 percent higher after puberty. Women tend to convert more food into fat, while men convert more into muscle and expendable circulating energy reserves. Women (on average) are about 52 percent as strong as men in the upper body, and about 66 percent as strong in the lower.[4] Men, on average, have denser, stronger bones, tendons, and ligaments. Although these differences may seem to indicate a natural predilection amongst human males for "heavier work", the sexual division of labour is a cultural issue, and not the point or intention of sexual dimorphism[5]
Men dissipate heat faster than women through their sweat glands.[citation needed] Women have a greater insulation and energy reserves stored in subcutaneous fat, absorbing endothermic heat less and retaining exothermic heat to a greater degree.[citation needed] Sex differences in endurance events are less significant than for sprinting events.[citation needed]
Men typically have larger tracheae and branching bronchi, with about 30 percent greater lung volume per body mass. They have larger hearts, 10 percent higher red blood cell count, higher hemoglobin, hence greater oxygen-carrying capacity. They also have higher circulating clotting factors (vitamin K, prothrombin and platelets). These differences lead to faster healing of wounds and higher peripheral pain tolerance.[5]
Women typically have more white blood cells (stored and circulating), more granulocytes and B and T lymphocytes. Additionally, they produce more antibodies at a faster rate than men. Hence they develop fewer infectious diseases and succumb for shorter periods.[5] Ethologists argue that women, interacting with other women and multiple offspring in social groups, have experienced such traits as a selective advantage.[6][7][8][9][10] Note that almost all examples of sexual dimorphism in humans are quantitative, and have some degree of overlap.
Some biologists theorise that a species' degree of sexual dimorphism is inversely related to the degree of paternal investment in parenting. Species with the highest sexual dimorphism, such as the pheasant, tend to be those species in which the care and raising of offspring is done only by the mother, with no involvement of the father (low degree of paternal investment).
Although there are many biologically-determined, sexually-dimorphic behaviours in other species, these have few, if any, implications for human society. However, analysis of sexually dimorphic human behavior naturally provokes controversy. One less controversial, but still hypothetical, area with considerable discussion in academic literature concerns potential evolutionary advantages associated with sexual competition (both intrasexual and intersexual) and short- and long-term sexual strategies.[11]
According to Daly and Wilson, "The sexes differ more in human beings than in monogamous mammals, but much less than in extremely polygamous mammals."[12]
D.M. Buss stated that "Males should prefer attributes in potential mates associated with reproductive value or fertility, depending on whether males in human evolutionary history have tended to seek long-term or short-term mating partners.[13] Specifically, if males in our evolutionary past have tended to seek short-term mating partners, selection should have favoured male preferences for females in their early 20s who show cues positively correlated with fertility. If males in our evolutionary past tended to seek long-term mating partners, selection should have favoured preferences for females in their mid-teens who show cues indicative of reproductive value. Evolutionary theorists differ on which of these they judge to be most likely."[14]
[edit] Sexual dimorphism in birds
Sexual dimorphism varies in bird species from very obvious differences, such as the plumage of male Peacocks, the greatly larger form of female eagles, to very similar appearance (most parrots).
When the appearance of the male and female is very similar they are called 'Monomorphic birds'[2]. The gender of Monomorphic birds is commonly revealed by endoscopic examination or surgical sexing [3]
Male birds such as canaries or parrots are occasionally mentioned by fanciers as being better singers or mimics than females, perhaps due to stronger attention- and territory-seeking behaviors, and are commonly sought out more frequently in the pet trade as a result.
[edit] See also
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Look up sexual dimorphism in Wiktionary, the free dictionary. |
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Wikimedia Commons has media related to: sexual dimorphism |
- Sexual dimorphism in non-human primates
- Bateman's principle
- Digit ratio
- Operational sex ratio
- Sexual selection
- Sexual differentiation
- Sexually dimorphic nucleus
- Sexual dimorphism measures
- Sexual reproduction
- Sex-limited genes
- Gender differences
- List of homologues of the human reproductive system
[edit] References
- ^ Lindenfors P, Gittleman JL & Jones KE, Sexual size dimorphism in mammals, in: Fairbairn DJ, Blanckenhorn WU & Szekely T (eds) Sex, size and gender roles: evolutionary studies of sexual size dimorphism (Oxford: Oxford University Press, 2007), pages 19-26
- ^ Arnqvist, Göran , Therésa M. Jones, Mark A. Elgar (2003)Reversal of sex roles in nuptial feeding. Nature 424:387 [1]
- ^ Gray 1918, Nowell 1926, Green 2000, et al.
- ^ http://www.ncbi.nlm.nih.gov/pubmed/8477683
- ^ a b c . A Glucksman, Sexual Dimorphism in Human and Mammalian Biology and Pathology, (Academic Press, 1981).
- ^ J Durden-Smith and D Desimone, Sex and the Brain, (New York: Arbor House, 1983).
- ^ ES Gersh and I Gersh, Biology of Women, (Baltimore: University Park Press, 1981).
- ^ J Stein (editor), Internal Medicine, 2nd edition., (Boston: Little, Brown and Company, 1987).
- ^ M McLaughlin and T Shryer, 'Men vs Women: The New Debate Over Sex Differences', U.S. News & World Report 8 August (1988): pp. 50-58.
- ^ BS McEwen, 'Neural Gonadal Steroid Action', Science 211 (1981): 1303–1311.
- ^ (David M Buss, 2007)
- ^ Martin Daly and Margo Wilson, 'Evolutionary Psychology and Marital Conflict', in Sex, Power, Conflict: Evolutionary and Feminist Perspectives, edited by DM Buss and Neil M Malamuth, (Oxford University Press, 1996), p. 13.
- ^ (Buss 1987; Symons 1979; Williams 1975)
- ^ DM Buss, 'Evolutionary theory', in Personality: Critical Concepts, edited by Cary L Cooper and Lawrence A Pervin, (Routledge, 1998), p. 422.
- Bonduriansky, R. (2007) The evolution of condition-dependent sexual dimorphism. The American Naturalist, 169:1 pp9–19.
- Biological Journal of the Linnean Society (1999), 67: 1–18.
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