Literature DB >> 3228171

Sexual selection and canine dimorphism in New World monkeys.

R F Kay1, J M Plavcan, K E Glander, P C Wright.   

Abstract

Social and ecological factors are important in shaping sexual dimorphism in Anthropoidea, but there is also a tendency for body-size dimorphism and canine dimorphism to increase with increased body size (Rensch's rule) (Rensch: Evolution Above the Species Level. London: Methuen, 1959.) Most ecologist interpret Rensch's rule to be a consequence of social and ecological selective factors that covary with body size, but recent claims have been advanced that dimorphism is principally a consequence of selection for increased body size alone. Here we assess the effects of body size, body-size dimorphism, and social structure on canine dimorphism among platyrrhine monkeys. Platyrrhine species examined are classified into four behavioral groups reflecting the intensity of intermale competition for access to females or to limiting resources. As canine dimorphism increases, so does the level of intermale competition. Those species with monogamous and polyandrous social structures have the lowest canine dimorphism, while those with dominance rank hierarchies of males have the most canine dimorphism. Species with fission-fusion social structures and transitory intermale breeding-season competition fall between these extremes. Among platyrrhines there is a significant positive correlation between body size and canine dimorphism However, within levels of competition, no significant correlation was found between the two. Also, with increased body size, body-size dimorphism tends to increase, and this correlation holds in some cases within competition levels. In an analysis of covariance, once the level of intermale competition is controlled for, neither molar size nor molar-size dimorphism accounts for a significant part of the variance in canine dimorphism. A similar analysis using body weight as a measure of size and dimorphism yields a less clear-cut picture: body weight contributes significantly to the model when the effects of the other factors are controlled. Finally, in a model using head and body length as a measure of size and dimorphism, all factors and the interactions between them are significant. We conclude that intermale competition among platyrrhine species is the most important factor explaining variations in canine dimorphism. The significant effects of size and size dimorphism in some models may be evidence that natural (as opposed to sexual) selection also plays a role in the evolution of increased canine dimorphism.

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Year:  1988        PMID: 3228171     DOI: 10.1002/ajpa.1330770311

Source DB:  PubMed          Journal:  Am J Phys Anthropol        ISSN: 0002-9483            Impact factor:   2.868


  10 in total

1.  The earliest fossil evidence for sexual dimorphism in primates.

Authors:  L Krishtalka; R K Stucky; K C Beard
Journal:  Proc Natl Acad Sci U S A       Date:  1990-07       Impact factor: 11.205

2.  Sexual size dimorphism, canine dimorphism, and male-male competition in primates: where do humans fit in?

Authors:  J Michael Plavcan
Journal:  Hum Nat       Date:  2012-03

3.  [Lemurs of Madagascar. Tests on evolution of primate communities].

Authors:  J U Ganzhorn; P M Kappeler
Journal:  Naturwissenschaften       Date:  1993-05

4.  Canine sexual dimorphism in Ardipithecus ramidus was nearly human-like.

Authors:  Gen Suwa; Tomohiko Sasaki; Sileshi Semaw; Michael J Rogers; Scott W Simpson; Yutaka Kunimatsu; Masato Nakatsukasa; Reiko T Kono; Yingqi Zhang; Yonas Beyene; Berhane Asfaw; Tim D White
Journal:  Proc Natl Acad Sci U S A       Date:  2021-12-07       Impact factor: 12.779

Review 5.  Why are there apes? Evidence for the co-evolution of ape and monkey ecomorphology.

Authors:  Kevin D Hunt
Journal:  J Anat       Date:  2016-04       Impact factor: 2.610

6.  The onset of puberty in colony-housed male and female titi monkeys (Plecturocebus cupreus): Possible effects of oxytocin treatment during peri-adolescent development.

Authors:  A J Conley; T Berger; R Arias Del Razo; R F Cotterman; E Sahagún; L R Goetze; S Jacob; T A R Weinstein; M E Dufek; S P Mendoza; K L Bales
Journal:  Horm Behav       Date:  2022-03-23       Impact factor: 3.492

7.  Canine length in wild male baboons: maturation, aging and social dominance rank.

Authors:  Jordi Galbany; Jenny Tung; Jeanne Altmann; Susan C Alberts
Journal:  PLoS One       Date:  2015-05-07       Impact factor: 3.240

8.  Variation in craniomandibular morphology and sexual dimorphism in pantherines and the sabercat Smilodon fatalis.

Authors:  Per Christiansen; John M Harris
Journal:  PLoS One       Date:  2012-10-26       Impact factor: 3.240

Review 9.  Eco-evo-devo of the lemur syndrome: did adaptive behavioral plasticity get canalized in a large primate radiation?

Authors:  Peter M Kappeler; Claudia Fichtel
Journal:  Front Zool       Date:  2015-08-24       Impact factor: 3.172

10.  A comparison of blood gases, biochemistry, and hematology to ecomorphology in a health assessment of pinfish (Lagodon rhomboides).

Authors:  Sara Collins; Alex Dornburg; Joseph M Flores; Daniel S Dombrowski; Gregory A Lewbart
Journal:  PeerJ       Date:  2016-08-09       Impact factor: 2.984

  10 in total

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