Literature DB >> 29641923

Detection of Fruit and the Selection of Primate Visual Pigments for Color Vision.

D Osorio, A C Smith, M Vorobyev, H M Buchanan-Smith.   

Abstract

Primates have X chromosome genes for cone photopigments with sensitivity maxima from 535 to 562 nm. Old World monkeys and apes (catarrhines) and the New World (platyrrhine) genus Alouatta have separate genes for 535-nm (medium wavelength; M) and 562-nm (long wavelength; L) pigments. These pigments, together with a 425-nm (short wavelength) pigment, permit trichromatic color vision. Other platyrrhines and prosimians have a single X chromosome gene but often with alleles for two or three M/L photopigments. Consequently, heterozygote females are trichromats, but males and homozygote females are dichromats. The criteria that affect the evolution of M/L alleles and maintain genetic polymorphism remain a puzzle, but selection for finding food may be important. We compare different types of color vision for detecting more than 100 plant species consumed by tamarins (Saguinus spp.) in Peru. There is evidence that both frequency-dependent selection on homozygotes and heterozygote advantage favor M/L polymorphism and that trichromatic color vision is most advantageous in dim light. Also, whereas the 562-nm allele is present in all species, the occurrence of 535- to 556-nm alleles varies between species. This variation probably arises because trichromatic color vision favors widely separated pigments and equal frequencies of 535/543- and 562-nm alleles, whereas in dichromats, long-wavelength pigment alleles are fitter.

Entities:  

Keywords:  balancing selection; color vision; evolution; modeling; primate

Year:  2004        PMID: 29641923     DOI: 10.1086/425332

Source DB:  PubMed          Journal:  Am Nat        ISSN: 0003-0147            Impact factor:   3.926


  25 in total

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Review 2.  Evolution of colour vision in mammals.

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Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2009-10-12       Impact factor: 6.237

3.  A foraging advantage for dichromatic marmosets (Callithrix geoffroyi) at low light intensity.

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Review 4.  The marmoset monkey as a model for visual neuroscience.

Authors:  Jude F Mitchell; David A Leopold
Journal:  Neurosci Res       Date:  2015-02-13       Impact factor: 3.304

5.  Trichromacy increases fruit intake rates of wild capuchins (Cebus capucinus imitator).

Authors:  Amanda D Melin; Kenneth L Chiou; Emily R Walco; Mackenzie L Bergstrom; Shoji Kawamura; Linda M Fedigan
Journal:  Proc Natl Acad Sci U S A       Date:  2017-09-11       Impact factor: 11.205

Review 6.  Seeing the rainbow: mechanisms underlying spectral sensitivity in teleost fishes.

Authors:  Karen L Carleton; Daniel Escobar-Camacho; Sara M Stieb; Fabio Cortesi; N Justin Marshall
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7.  Avian egg and nestling detection in the wild: should we rely on visual models or behavioural experiments?

Authors:  Jesús M Avilés
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2020-05-18       Impact factor: 6.237

8.  Chimpanzee (Pan troglodytes) gaze is conspicuous at ecologically-relevant distances.

Authors:  Will Whitham; Steven J Schapiro; Jolyon Troscianko; Jessica L Yorzinski
Journal:  Sci Rep       Date:  2022-06-03       Impact factor: 4.996

9.  Adaptive evolution of color vision as seen through the eyes of butterflies.

Authors:  Francesca D Frentiu; Gary D Bernard; Cristina I Cuevas; Marilou P Sison-Mangus; Kathleen L Prudic; Adriana D Briscoe
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-09       Impact factor: 11.205

10.  Color signal information content and the eye of the beholder: a case study in the rhesus macaque.

Authors:  James P Higham; Lauren J N Brent; Constance Dubuc; Amanda K Accamando; Antje Engelhardt; Melissa S Gerald; Michael Heistermann; Martin Stevens
Journal:  Behav Ecol       Date:  2010-04-15       Impact factor: 2.671

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