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Butterfly dichromatism primarily evolved via Darwin's, not Wallace's, model
Sexual dimorphism is typically thought to result from sexual selection for elaborated male traits, as proposed by Darwin. However, natural selection could reduce expression of elaborated traits in females, as proposed by Wallace. Darwin and Wallace debated the origins of dichromatism in birds and bu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719551/ https://www.ncbi.nlm.nih.gov/pubmed/33312689 http://dx.doi.org/10.1002/evl3.199 |
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author | van der Bijl, Wouter Zeuss, Dirk Chazot, Nicolas Tunström, Kalle Wahlberg, Niklas Wiklund, Christer Fitzpatrick, John L. Wheat, Christopher W. |
author_facet | van der Bijl, Wouter Zeuss, Dirk Chazot, Nicolas Tunström, Kalle Wahlberg, Niklas Wiklund, Christer Fitzpatrick, John L. Wheat, Christopher W. |
author_sort | van der Bijl, Wouter |
collection | PubMed |
description | Sexual dimorphism is typically thought to result from sexual selection for elaborated male traits, as proposed by Darwin. However, natural selection could reduce expression of elaborated traits in females, as proposed by Wallace. Darwin and Wallace debated the origins of dichromatism in birds and butterflies, and although evidence in birds is roughly equal, if not in favor of Wallace's model, butterflies lack a similar scale of study. Here, we present a large‐scale comparative phylogenetic analysis of the evolution of butterfly coloration, using all European non‐hesperiid butterfly species (n = 369). We modeled evolutionary changes in coloration for each species and sex along their phylogeny, thereby estimating the rate and direction of evolution in three‐dimensional color space using a novel implementation of phylogenetic ridge regression. We show that male coloration evolved faster than female coloration, especially in strongly dichromatic clades, with male contribution to changes in dichromatism roughly twice that of females. These patterns are consistent with a classic Darwinian model of dichromatism via sexual selection on male coloration, suggesting this model was the dominant driver of dichromatism in European butterflies. |
format | Online Article Text |
id | pubmed-7719551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77195512020-12-11 Butterfly dichromatism primarily evolved via Darwin's, not Wallace's, model van der Bijl, Wouter Zeuss, Dirk Chazot, Nicolas Tunström, Kalle Wahlberg, Niklas Wiklund, Christer Fitzpatrick, John L. Wheat, Christopher W. Evol Lett Letters Sexual dimorphism is typically thought to result from sexual selection for elaborated male traits, as proposed by Darwin. However, natural selection could reduce expression of elaborated traits in females, as proposed by Wallace. Darwin and Wallace debated the origins of dichromatism in birds and butterflies, and although evidence in birds is roughly equal, if not in favor of Wallace's model, butterflies lack a similar scale of study. Here, we present a large‐scale comparative phylogenetic analysis of the evolution of butterfly coloration, using all European non‐hesperiid butterfly species (n = 369). We modeled evolutionary changes in coloration for each species and sex along their phylogeny, thereby estimating the rate and direction of evolution in three‐dimensional color space using a novel implementation of phylogenetic ridge regression. We show that male coloration evolved faster than female coloration, especially in strongly dichromatic clades, with male contribution to changes in dichromatism roughly twice that of females. These patterns are consistent with a classic Darwinian model of dichromatism via sexual selection on male coloration, suggesting this model was the dominant driver of dichromatism in European butterflies. John Wiley and Sons Inc. 2020-10-23 /pmc/articles/PMC7719551/ /pubmed/33312689 http://dx.doi.org/10.1002/evl3.199 Text en © 2020 The Authors. Evolution Letters published by Wiley Periodicals, LLC on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letters van der Bijl, Wouter Zeuss, Dirk Chazot, Nicolas Tunström, Kalle Wahlberg, Niklas Wiklund, Christer Fitzpatrick, John L. Wheat, Christopher W. Butterfly dichromatism primarily evolved via Darwin's, not Wallace's, model |
title | Butterfly dichromatism primarily evolved via Darwin's, not Wallace's, model |
title_full | Butterfly dichromatism primarily evolved via Darwin's, not Wallace's, model |
title_fullStr | Butterfly dichromatism primarily evolved via Darwin's, not Wallace's, model |
title_full_unstemmed | Butterfly dichromatism primarily evolved via Darwin's, not Wallace's, model |
title_short | Butterfly dichromatism primarily evolved via Darwin's, not Wallace's, model |
title_sort | butterfly dichromatism primarily evolved via darwin's, not wallace's, model |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719551/ https://www.ncbi.nlm.nih.gov/pubmed/33312689 http://dx.doi.org/10.1002/evl3.199 |
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