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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...

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Autores principales: van der Bijl, Wouter, Zeuss, Dirk, Chazot, Nicolas, Tunström, Kalle, Wahlberg, Niklas, Wiklund, Christer, Fitzpatrick, John L., Wheat, Christopher W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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