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Ocular pigmentation in humans, great apes, and gibbons is not suggestive of communicative functions
Pigmentation patterns of the visible part of the eyeball, encompassing the iris and portions of the sclera, have been discussed to be linked to social cognition in primates. The cooperative eye hypothesis suggests the white sclera of humans to be a derived adaptive trait that enhances eye-mediated c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217224/ https://www.ncbi.nlm.nih.gov/pubmed/34155285 http://dx.doi.org/10.1038/s41598-021-92348-z |
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author | Caspar, Kai R. Biggemann, Marco Geissmann, Thomas Begall, Sabine |
author_facet | Caspar, Kai R. Biggemann, Marco Geissmann, Thomas Begall, Sabine |
author_sort | Caspar, Kai R. |
collection | PubMed |
description | Pigmentation patterns of the visible part of the eyeball, encompassing the iris and portions of the sclera, have been discussed to be linked to social cognition in primates. The cooperative eye hypothesis suggests the white sclera of humans to be a derived adaptive trait that enhances eye-mediated communication. Here, we provide a comparative analysis of ocular pigmentation patterns in 15 species of hominoids (humans, great apes & gibbons) that show marked differences in social cognition and quantify scleral exposure at the genus level. Our data reveals a continuum of eye pigmentation traits in hominoids which does not align with the complexity of gaze-mediated communication in the studied taxa. Gibbons display darker eyes than great apes and expose less sclera. Iridoscleral contrasts in orangutans and gorillas approach the human condition but differ between congeneric species. Contrary to recent discussions, we found chimpanzee eyes to exhibit a cryptic coloration scheme that resembles gibbons more than other apes. We reevaluate the evidence for links between social cognition and eye pigmentation in primates, concluding that the cooperative eye hypothesis cannot explain the patterns observed. Differences in scleral pigmentation between great apes and humans are gradual and might have arisen via genetic drift and sexual selection. |
format | Online Article Text |
id | pubmed-8217224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82172242021-06-22 Ocular pigmentation in humans, great apes, and gibbons is not suggestive of communicative functions Caspar, Kai R. Biggemann, Marco Geissmann, Thomas Begall, Sabine Sci Rep Article Pigmentation patterns of the visible part of the eyeball, encompassing the iris and portions of the sclera, have been discussed to be linked to social cognition in primates. The cooperative eye hypothesis suggests the white sclera of humans to be a derived adaptive trait that enhances eye-mediated communication. Here, we provide a comparative analysis of ocular pigmentation patterns in 15 species of hominoids (humans, great apes & gibbons) that show marked differences in social cognition and quantify scleral exposure at the genus level. Our data reveals a continuum of eye pigmentation traits in hominoids which does not align with the complexity of gaze-mediated communication in the studied taxa. Gibbons display darker eyes than great apes and expose less sclera. Iridoscleral contrasts in orangutans and gorillas approach the human condition but differ between congeneric species. Contrary to recent discussions, we found chimpanzee eyes to exhibit a cryptic coloration scheme that resembles gibbons more than other apes. We reevaluate the evidence for links between social cognition and eye pigmentation in primates, concluding that the cooperative eye hypothesis cannot explain the patterns observed. Differences in scleral pigmentation between great apes and humans are gradual and might have arisen via genetic drift and sexual selection. Nature Publishing Group UK 2021-06-21 /pmc/articles/PMC8217224/ /pubmed/34155285 http://dx.doi.org/10.1038/s41598-021-92348-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Caspar, Kai R. Biggemann, Marco Geissmann, Thomas Begall, Sabine Ocular pigmentation in humans, great apes, and gibbons is not suggestive of communicative functions |
title | Ocular pigmentation in humans, great apes, and gibbons is not suggestive of communicative functions |
title_full | Ocular pigmentation in humans, great apes, and gibbons is not suggestive of communicative functions |
title_fullStr | Ocular pigmentation in humans, great apes, and gibbons is not suggestive of communicative functions |
title_full_unstemmed | Ocular pigmentation in humans, great apes, and gibbons is not suggestive of communicative functions |
title_short | Ocular pigmentation in humans, great apes, and gibbons is not suggestive of communicative functions |
title_sort | ocular pigmentation in humans, great apes, and gibbons is not suggestive of communicative functions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217224/ https://www.ncbi.nlm.nih.gov/pubmed/34155285 http://dx.doi.org/10.1038/s41598-021-92348-z |
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