Color Discrimination in the Tufted Capuchin Monkey, Sapajus spp

Citation metadata

From: PLoS ONE(Vol. 8, Issue 4)
Publisher: Public Library of Science
Document Type: Article
Length: 6,577 words
Lexile Measure: 1530L

Document controls

Main content

Article Preview :

Author(s): Paulo Roney Kilpp Goulart 1,*, Daniela Maria Oliveira Bonci 2,3, Olavo de Faria Galvão 1, Luiz Carlos de Lima Silveira 4,5, Dora Fix Ventura 2,3

Introduction

The first behavioral studies on color vision in New World monkeys (platyrrhine primates) were performed with capuchin monkeys at the end of the 1930s [1], [2]. The three male capuchins in these studies that were subjected to experiments on wavelength discrimination, color matching, and neutral points of spectral sensitivity showed reduced sensitivity at the long-wavelength end of the spectrum compared with humans and other catarrhine primates (i.e., Old World monkeys) evaluated with similar tests. This finding seemed to indicate that capuchin monkeys had color vision phenotypes that were similar to those of protanopic humans and that the New World monkeys could be used to study intermediate evolutionary stages of trichromatic color vision.

Additional behavioral studies and biological investigations with other New World monkeys, especially squirrel monkeys (Saimiri sp.), demonstrated the occurrence of intraspecies phenotypic variations [3]-[5]. Electrophysiological [4]-[8] and genetic [9], [10] investigations documented the occurrence of multiple M/L photopigments in platyrrhine monkeys related to the presence of a single polymorphic gene on the X chromosome that encodes M/L photopigments. According to the resulting model, New World monkeys have a sex-linked polymorphic gene for color vision, with some females being trichromats and all of the males and the remainder of females being dichromats. In these polymorphic species, the X chromosome possesses a single gene that is responsible for the expression of cone photopigments, with multiple allelic versions that occur in the same species [11]-[14]. Each allele is responsible for minute variations in the amino acid sequence that composes the protein portion (opsin) of the photopigment. These variations, in turn, translate to differences in photopigment sensitivity along the medium- to long-wavelength region of the light spectrum. Similar genotype/phenotype arrangements have been observed in the majority of the New World monkeys studied to date, including capuchin monkeys [10], [15], [16].

Three variants of medium/long-wavelength-sensitive photopigments have been consistently described for capuchin monkeys, with spectral peaks near 530, 550, and 560 nm [14], herein referred to as M, ML, and L photopigments, respectively. The different combinations of short-wavelength (S)-sensitive photopigments and medium/long-wavelength-sensitive photopigments produce six different color vision phenotypes within the same population. Heterozygous females (i.e. those that have a different allele in each of their X chromosomes) express two different medium/long wavelength-sensitive photoreceptors. Depending on the specific alleles present, each individual shows one of three trichromatic phenotypes (S-M-L, S-M-ML, or S-ML-L). In contrast, homozygous females and males express only one of the three possible medium/long-wavelength-sensitive cone photoreceptors. Each individual then shows one of three dichromatic phenotypes (S-M, S-ML, S-L).

Decades of accumulated knowledge on the interactions among opsin genes, photopigments, and the behavioral expression of color vision in New World monkeys has made the prediction of color discrimination capabilities of these animals based on their anatomical and physiological attributes a common practice. Monkeys that possess two cone opsins (all males and homozygous females) are...

Source Citation

Source Citation   

Gale Document Number: GALE|A478215440