ne·ot·e·ny [nee-ot-n-ee] –noun Biology.
1. Also called pedogenesis. the production of offspring by an organism in its larval or juvenile form; the elimination of the adult phase of the life cycle. 2. a slowing of the rate of development with the consequent retention in adulthood of a feature or features that appeared in an earlier phase in the life cycle of ancestral individuals: Neoteny in the ostrich has resulted in adult birds sporting the down feathers of nestlings. [Origin: 1900–05], Dictionary.com Unabridged (v 1.1). Random House, Inc. http://dictionary.reference.com/browse/neoteny (accessed: April 27, 2007).
Is Homo Sapiens a neotenic great ape? Did our ancestors (and still we) select for infantile traits in their choice of a mating partner? David Brin, in his essay Neoteny and Two-Way Sexual Selection in Human Evolution tries to explain this:
Our starting point is a perceived dichotomy between adult men and women — and thus potentially hazardous ground. Although evolutionary biology has lately been defended from a feminist perspective by Patricia Adair Gowaty (1992) and others, caution remains essential when stepping into this arena, hence I will at times seem to belabor the obvious. Let me also emphasize that Homo sapiens appears less riven by sexual dimorphism than most species, and exceptions exist to nearly every generalization. Nevertheless, it seems clear that past and present human dimorphisms are legitimate topics for careful discussion. While certain neotenous traits seem to be shared equally among the sexes (e.g., curiosity and plasticity of behavior), human females certainly do appear more paedomorphic in outward physical appearance than males. Although they mature at an earlier age, women do not go on to acquire the toughened skin, coarse body hair, thyroid cartilage, bony eye ridges, or deepened voices which are the common inheritance of most adult hominoids and other primates. Jones and Hill (1993) have shown that this generalization remains valid across racial, ethnic and cultural boundaries. Difference in degree of paedomorphism is one of the few truly decisive human sexual-dichotomies, used by most of us in visually distinguishing women from men.
Brin then covers the shift in courtship apparent in humans:
Why is it that a human female generally has to compete with other women to get a mate? May we stipulate that women do often vie over men? In one contemporary society, the United States, nearly all of the most popular magazines for women trumpet articles advising their readers how to stay competitive in what is portrayed as a desperate struggle to find and keep a mate. […] Now of course men compete over women, too. But among animals this is only normal. Except for some spermatophore-donating insects, and a few fish and birds, competition between males for sexual opportunity seems almost universal.
Read on for his conclusions.
Stephen Jay Gould wrote about human neoteny in his 1977 book Onthogeny and Phylogeny, here’s a quick quote:
To support the argument that we evolved by retaining juvenile features of our ancestors, Bolk provided lists of similarities between adult humans and juvenile apes: “Our essential somatic properties, i.e. those which distinguish the human body form from that of other Primates, have all one feature in common, viz they are fetal conditions that have become permanent. What is a transitional stage in the ontogensis of other Primates has become a terminal stage in man” (1926a, p. 468). In his most extensive work Bolk (1926c, p. 6) provided an abbreviated list in the following order:
1. Our “flat faced” orthognathy (a phenomenon of complex cause related both to facial reduction and to the retention of juvenile flexure, reflected, for example, in the failure of the sphenoethmoidal angle to open out during ontogeny).
2. Reduction of lack of body hair.
3. Loss of pigmentation in skin, eyes, and hair (Bolk argues that black peoples are born with relatively light skin, while ancestral primates are as dark at birth as ever).
4. The form of the external ear.
5. The epicanthic (or Mongolian) eyefold.
6. The central position of the foramen magnum (it migrates backward during the ontogeny of primates).
7. High relative brain weight.
8. Persistence of the cranial sutures to an advanced age.
9. The labia majora of women.
10. The structure of the hand and foot.
11. The form of the pelvis.
12. The ventrally directed position of the sexual canal in women.
13. Certain variations of the tooth row and cranial sutures.
To this basic list, Bolk added many additional features; other compendia are presented by Montagu (1962), de Beer (1948, 1958), and Keith (1949). The following items follow Montagu’s order (pp. 326-327) with some deletions and additions:
14. Absence of brow ridges.
15. Absence of cranial crests.
16. Thinness of skull bones.
17. Position of orbits under cranial cavity.
18. Brachycephaly.
19. Small teeth.
20. Late eruption of teeth.
21. No rotation of the big toe.
22. Prolonged period of infantile dependency.
23. Prolonged period of growth.
24. Long life span.
25. Large body size (related by Bolk, 1926c, p. 39, to retardation of ossification and retention of fetal growth rates).These lists from Bolk and Montagu display the extreme variation in type and importance of the basic data presented by leading supporters of human neoteny.” (Gould, S.J. (1977) Ontogeny and Phylogeny, Cambridge: Belknap Press. p. 357)
“Humans and chimps are almost identical in structural gens, yet differ markedly in form and behavior. This paradox can be resolved by invoking a small genetic difference with profound effects—alterations in the regulatory system that slow down the general rate of development in humans. Heterochronic changes are regulatory changes; they require only an alteration in the timing of features already present. If the frequency of heterochronic change were known, it would provide a good estimate for the importance of regulation as an evolutionary agent” (Gould, S.J. (1977) Ontegeny and Phylogeny. Cambridge: Belknap Press. p. 9)
“Evolution occurs when ontogeny is altered in one of two ways: when new characters are introduced at any stage of development with varying effects upon subsequent stages, or when characters already present undergo changes in developmental timing. Together, these two processes exhaust the formal content of phyletic change; the second process is heterochrony. If change in developmental timing is important in evolution, then this second process must be very common (if it is predominant in frequency, I will be in even better shape).” (Gould, S.J. (1977) Onthogeny and Phylogeny. Cambridge: Belknap Press.pp. 4. Retrieved from this site)
I can quote also The Feminine Beauty website (which has a lexical exception):
Whereas above average femininity is a powerful correlate of beauty in women, neoteny isn’t even though many researchers continue to point this out. Elsewhere within this site, it has been shown that neoteny, which is the retention in the adult of the features of the juvenile stages of the ancestral species, does not apply to the shape of the human face. The authors were trying to imply pedomorphy as a correlate of beauty but incorrectly used the term neoteny. Pedomorphy refers to the retention in the adult of more child-like features. Whereas it is true that the faces of women are closer to those of children, sexual maturity makes both males and females move away from the face shape of children, and the central tendency of adults is to prefer sexually mature individuals. Therefore, it is incorrect to describe pedomorphy as a correlate of beauty when more attractive features that appear to be pedomorphic are either somewhat more feminine than average features (e.g., less prominent noses and broader faces, controlling for other factors) and thereby more attractive in women or somewhat more gracile than average features and thereby more attractive in both men and women.
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