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The adaptive significance of human scleral brightness: an experimental study
Homogeneously depigmented sclerae have long been proposed to be uniquely human—an adaptation to enable cooperative behaviour by facilitating interpersonal coordination through gaze following. However, recent evidence has shown that deeply pigmented sclerae also afford gaze following if surrounding a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691750/ https://www.ncbi.nlm.nih.gov/pubmed/36424405 http://dx.doi.org/10.1038/s41598-022-24403-2 |
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author | Wacewicz, Slawomir Perea-García, Juan Olvido Lewandowski, Zdzisław Danel, Dariusz P. |
author_facet | Wacewicz, Slawomir Perea-García, Juan Olvido Lewandowski, Zdzisław Danel, Dariusz P. |
author_sort | Wacewicz, Slawomir |
collection | PubMed |
description | Homogeneously depigmented sclerae have long been proposed to be uniquely human—an adaptation to enable cooperative behaviour by facilitating interpersonal coordination through gaze following. However, recent evidence has shown that deeply pigmented sclerae also afford gaze following if surrounding a bright iris. Furthermore, while current scleral depigmentation is clearly adaptive in modern humans, it is less clear how the evolutionarily intermediate stages of scleral pigmentation may have been adaptive. In sum, it is unclear why scleral depigmentation became the norm in humans, while not so in sister species like chimpanzees, or why some extant species display intermediate degrees of pigmentation (as our ancestors presumably did at some point). We created realistic facial images of 20 individually distinct hominins with diverse facial morphologies, each face in the (i) humanlike bright sclera and (ii) generalised apelike dark sclera version. Participants in two online studies rated the bright-sclera hominins as younger, healthier, more attractive and trustworthy, but less aggressive than the dark-sclera hominins. Our results support the idea that the appearance of more depigmented sclerae promoted perceived traits that fostered trust, increasing fitness for those individuals and resulting in depigmentation as a fixed trait in extant humans. |
format | Online Article Text |
id | pubmed-9691750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96917502022-11-26 The adaptive significance of human scleral brightness: an experimental study Wacewicz, Slawomir Perea-García, Juan Olvido Lewandowski, Zdzisław Danel, Dariusz P. Sci Rep Article Homogeneously depigmented sclerae have long been proposed to be uniquely human—an adaptation to enable cooperative behaviour by facilitating interpersonal coordination through gaze following. However, recent evidence has shown that deeply pigmented sclerae also afford gaze following if surrounding a bright iris. Furthermore, while current scleral depigmentation is clearly adaptive in modern humans, it is less clear how the evolutionarily intermediate stages of scleral pigmentation may have been adaptive. In sum, it is unclear why scleral depigmentation became the norm in humans, while not so in sister species like chimpanzees, or why some extant species display intermediate degrees of pigmentation (as our ancestors presumably did at some point). We created realistic facial images of 20 individually distinct hominins with diverse facial morphologies, each face in the (i) humanlike bright sclera and (ii) generalised apelike dark sclera version. Participants in two online studies rated the bright-sclera hominins as younger, healthier, more attractive and trustworthy, but less aggressive than the dark-sclera hominins. Our results support the idea that the appearance of more depigmented sclerae promoted perceived traits that fostered trust, increasing fitness for those individuals and resulting in depigmentation as a fixed trait in extant humans. Nature Publishing Group UK 2022-11-24 /pmc/articles/PMC9691750/ /pubmed/36424405 http://dx.doi.org/10.1038/s41598-022-24403-2 Text en © The Author(s) 2022 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 Wacewicz, Slawomir Perea-García, Juan Olvido Lewandowski, Zdzisław Danel, Dariusz P. The adaptive significance of human scleral brightness: an experimental study |
title | The adaptive significance of human scleral brightness: an experimental study |
title_full | The adaptive significance of human scleral brightness: an experimental study |
title_fullStr | The adaptive significance of human scleral brightness: an experimental study |
title_full_unstemmed | The adaptive significance of human scleral brightness: an experimental study |
title_short | The adaptive significance of human scleral brightness: an experimental study |
title_sort | adaptive significance of human scleral brightness: an experimental study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691750/ https://www.ncbi.nlm.nih.gov/pubmed/36424405 http://dx.doi.org/10.1038/s41598-022-24403-2 |
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