Secondary sex characteristic

[1]Secondary sex characteristics are features that appear during puberty in humans, and at sexual maturity in other animals.[2][3] These characteristics are particularly evident in the sexually dimorphic phenotypic traits that distinguish the sexes of a species,[4] but--unlike the sex organs (primary sex characteristics)--are not directly part of the reproductive system.[5] Secondary sex characteristics are believed to be the product of sexual selection for traits which display fitness, giving an organism an advantage over its rivals in courtship and in aggressive interactions.[6]

A peacock displays his long, colored tail, an example of secondary sex characteristics

Secondary sex characteristics include, for example, the manes of male lions,[3] the bright facial and rump coloration of male mandrills, and horns in many goats and antelopes. These characteristics are believed to be produced by a positive feedback loop known as the Fisherian runaway produced by the secondary characteristic in one sex and the desire for that characteristic in the other sex. Male birds and fish of many species have brighter coloration or other external ornaments. Differences in size between sexes are also considered secondary sexual characteristics.

In humans, visible secondary sex characteristics include pubic hair, enlarged breasts and widened hips of females, and facial hair and Adam's apples on males.[5][7]

Evolutionary roots
A red deer stag's antlers are secondary sexual characteristics.

Charles Darwin hypothesized that sexual selection, or competition within a species for mates, can explain observed differences between sexes in many species.[8]

Ronald Fisher, the English biologist developed a number of ideas concerning secondary characteristics in his 1930 book The Genetical Theory of Natural Selection, including the concept of Fisherian runaway which postulates that the desire for a characteristic in females combined with that characteristic in males can create a positive feedback loop or runaway where the feature becomes hugely amplified. The 1975 handicap principle extends this idea, stating that a peacock's tail, for instance, displays fitness by being a useless impediment that is very hard to fake. Another of Fisher's ideas is the sexy son hypothesis, whereby females will desire to have sons that possess the characteristic that they find sexy in order to maximize the number of grandchildren they produce.[9] An alternative hypothesis is that some of the genes that enable males to develop impressive ornaments or fighting ability may be correlated with fitness markers such as disease resistance or a more efficient metabolism. This idea is known as the good genes hypothesis.

In non-human animals

Secondary sex characteristics in non-human animals include manes of male lions[3] and long feathers of male peafowl, the tusks of male narwhals, enlarged proboscises in male elephant seals and proboscis monkeys, the bright facial and rump coloration of male mandrills, and horns in many goats and antelopes.

Biologists today distinguish between "male-to-male combat" and "mate choice", usually female choice of male mates. Sexual characteristics due to combat are such things as antlers, horns, and greater size. Characteristics due to mate choice, often referred to as ornaments, include brighter plumage, coloration, and other features that have no immediate purpose for survival or combat.

Male jumping spiders have visual patches of UV reflectance, which are ornamentations used to attract females.[10]

In humans
Anatomical characteristics of the human male and female

Sexual differentiation begins during gestation, when the gonads are formed. The general structure and shape of the body and face, as well as sex hormone levels, are similar in preadolescent boys and girls. As puberty begins and sex hormone levels rise, differences appear, though some changes are similar in males and females. Male levels of testosterone directly induce the growth of the genitals, and indirectly (via dihydrotestosterone (DHT)) the prostate. Estradiol and other hormones cause breasts to develop in females. However, fetal or neonatal androgens may modulate later breast development by reducing the capacity of breast tissue to respond to later estrogen.[11][12][13]

Underarm hair and pubic hair are usually considered secondary sex characteristics,[7] but they may also be considered non-secondary sex characteristics because they are features of both sexes following puberty.[14]

Females

In females, breasts are a manifestation of higher levels of estrogen; estrogen also widens the pelvis and increases the amount of body fat in hips, thighs, buttocks, and breasts.[5][7] Estrogen also induces growth of the uterus, proliferation of the endometrium, and menstruation.[5] Female secondary sex characteristics include:

Males

The increased secretion of testosterone from the testes during puberty causes the male secondary sexual characteristics to be manifested.[18] In males, testosterone directly increases size and mass of muscles, vocal cords, and bones, deepening the voice, and changing the shape of the face and skeleton.[5] Converted into DHT in the skin, it accelerates growth of androgen-responsive facial and body hair but may slow and eventually stop the growth of head hair. Taller stature is largely a result of later puberty and slower epiphyseal fusion. Male secondary sex characteristics include:

References
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  10. Lim, Matthew L. M., and Daiqin Li. "Courtship and Male-Male Agonistic Behaviour of Comsophasis Umbratica Simon, an Ornate Jumping Spider (Araneae: Salticidae)." The Raffles Bulletin of Zoology (2004): 52(2): 435-448. National University of Singapore. 20 September 2015
  11. G. Raspé (22 October 2013). Hormones and Embryonic Development: Advances in the Biosciences. Elsevier Science. pp. 32–. ISBN 978-1-4831-5171-7. The first genetic male child with a defect in 3β-hydroxy-Δ5-steroid oxidoreductase to have reached puberty has been reported to have a high level of 3β-hydroxy-A5 steroid excretion, hypospadias at birth, salt-wasting, and a history of two siblings with congenital adrenal hyperplasia and ambiguous genitalia [33]. Although at puberty he has signs of virilization, he has developed pronounced gynecomastia. Thus, this boy demonstrates that breast development may occur in postpubertal males if the programing of the pubertal sex differentiation of the mammary gland anlagen is disturbed by an enzyme defect which causes a failure of fetal testicular testosterone production. This observation is completely consistent with the findings in the experimental models [11, 32].
  12. Neumann F, Elger W (March 1967). "Steroidal stimulation of mammary glands in prenatally feminized male rats". Eur. J. Pharmacol. 1 (2): 120–3. doi:10.1016/0014-2999(67)90048-9. PMID 6070056. When administered to gravid rats during pregnancy an anti-androgenic steroid [cyproterone acetate] induced development of nipples in male fetuses. These nipples and associated glandular tissues develop after birth as in normal female animals. Progestin-estrogen treatment of adult, castrated feminized males produced stimulation of the glandular tissue similar to that seen after treatment of castrated female animals. In castrated male rats this treatment produces little glandular proliferation. It is concluded that androgens normally prevent the development of nipples and extensive formation of mammary tissue in male fetuses.
  13. Rajendran KG, Shah PN, Dubey AK, Bagli NP (1977). "Mammary gland differentiation in adult male rat--effect of prenatal exposure to cyproterone acetate". Endocr Res Commun. 4 (5): 267–74. doi:10.3109/07435807709052946. PMID 608453. Breast tissue of adult male Holtzman rats exposed to cyproterone acetate during embryonic differentiation showed presence of specific estradiol receptor proteins and C-19 steroid aromatase. We reported similar findings in gynecomastia in man. It is therefore proposed that gynecomastia probably results from failure of adequate testosterone action on the breast primordia during embryonic differentiation.
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