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Sexual selection predicts the rate and direction of colour divergence in a large avian radiation

Sexual selection is proposed to be a powerful driver of phenotypic evolution in animal systems. At macroevolutionary scales, sexual selection can theoretically drive both the rate and direction of phenotypic evolution, but this hypothesis remains contentious. Here, we find that differences in the ra...

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Autores principales: Cooney, Christopher R., Varley, Zoë K., Nouri, Lara O., Moody, Christopher J. A., Jardine, Michael D., Thomas, Gavin H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467902/
https://www.ncbi.nlm.nih.gov/pubmed/30992444
http://dx.doi.org/10.1038/s41467-019-09859-7
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author Cooney, Christopher R.
Varley, Zoë K.
Nouri, Lara O.
Moody, Christopher J. A.
Jardine, Michael D.
Thomas, Gavin H.
author_facet Cooney, Christopher R.
Varley, Zoë K.
Nouri, Lara O.
Moody, Christopher J. A.
Jardine, Michael D.
Thomas, Gavin H.
author_sort Cooney, Christopher R.
collection PubMed
description Sexual selection is proposed to be a powerful driver of phenotypic evolution in animal systems. At macroevolutionary scales, sexual selection can theoretically drive both the rate and direction of phenotypic evolution, but this hypothesis remains contentious. Here, we find that differences in the rate and direction of plumage colour evolution are predicted by a proxy for sexual selection intensity (plumage dichromatism) in a large radiation of suboscine passerine birds (Tyrannida). We show that rates of plumage evolution are correlated between the sexes, but that sexual selection has a strong positive effect on male, but not female, interspecific divergence rates. Furthermore, we demonstrate that rapid male plumage divergence is biased towards carotenoid-based (red/yellow) colours widely assumed to represent honest sexual signals. Our results highlight the central role of sexual selection in driving avian colour divergence, and reveal the existence of convergent evolutionary responses of animal signalling traits under sexual selection.
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spelling pubmed-64679022019-04-18 Sexual selection predicts the rate and direction of colour divergence in a large avian radiation Cooney, Christopher R. Varley, Zoë K. Nouri, Lara O. Moody, Christopher J. A. Jardine, Michael D. Thomas, Gavin H. Nat Commun Article Sexual selection is proposed to be a powerful driver of phenotypic evolution in animal systems. At macroevolutionary scales, sexual selection can theoretically drive both the rate and direction of phenotypic evolution, but this hypothesis remains contentious. Here, we find that differences in the rate and direction of plumage colour evolution are predicted by a proxy for sexual selection intensity (plumage dichromatism) in a large radiation of suboscine passerine birds (Tyrannida). We show that rates of plumage evolution are correlated between the sexes, but that sexual selection has a strong positive effect on male, but not female, interspecific divergence rates. Furthermore, we demonstrate that rapid male plumage divergence is biased towards carotenoid-based (red/yellow) colours widely assumed to represent honest sexual signals. Our results highlight the central role of sexual selection in driving avian colour divergence, and reveal the existence of convergent evolutionary responses of animal signalling traits under sexual selection. Nature Publishing Group UK 2019-04-16 /pmc/articles/PMC6467902/ /pubmed/30992444 http://dx.doi.org/10.1038/s41467-019-09859-7 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cooney, Christopher R.
Varley, Zoë K.
Nouri, Lara O.
Moody, Christopher J. A.
Jardine, Michael D.
Thomas, Gavin H.
Sexual selection predicts the rate and direction of colour divergence in a large avian radiation
title Sexual selection predicts the rate and direction of colour divergence in a large avian radiation
title_full Sexual selection predicts the rate and direction of colour divergence in a large avian radiation
title_fullStr Sexual selection predicts the rate and direction of colour divergence in a large avian radiation
title_full_unstemmed Sexual selection predicts the rate and direction of colour divergence in a large avian radiation
title_short Sexual selection predicts the rate and direction of colour divergence in a large avian radiation
title_sort sexual selection predicts the rate and direction of colour divergence in a large avian radiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467902/
https://www.ncbi.nlm.nih.gov/pubmed/30992444
http://dx.doi.org/10.1038/s41467-019-09859-7
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