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Disruptive natural selection predicts divergence between the sexes during adaptive radiation

Evolution of sexual dimorphism in ecologically relevant traits, for example, via resource competition between the sexes, is traditionally envisioned to stall the progress of adaptive radiation. An alternative view is that evolution of ecological sexual dimorphism could in fact play an important posi...

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Autores principales: De Lisle, Stephen P., Rowe, Locke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433998/
https://www.ncbi.nlm.nih.gov/pubmed/28515895
http://dx.doi.org/10.1002/ece3.2868
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author De Lisle, Stephen P.
Rowe, Locke
author_facet De Lisle, Stephen P.
Rowe, Locke
author_sort De Lisle, Stephen P.
collection PubMed
description Evolution of sexual dimorphism in ecologically relevant traits, for example, via resource competition between the sexes, is traditionally envisioned to stall the progress of adaptive radiation. An alternative view is that evolution of ecological sexual dimorphism could in fact play an important positive role by facilitating sex‐specific adaptation. How competition‐driven disruptive selection, ecological sexual dimorphism, and speciation interact during real adaptive radiations is thus a critical and open empirical question. Here, we examine the relationships between these three processes in a clade of salamanders that has recently radiated into divergent niches associated with an aquatic life cycle. We find that morphological divergence between the sexes has occurred in a combination of head shape traits that are under disruptive natural selection within breeding ponds, while divergence among species means has occurred independently of this disruptive selection. Further, we find that adaptation to aquatic life is associated with increased sexual dimorphism across taxa, consistent with the hypothesis of clade‐wide character displacement between the sexes. Our results suggest the evolution of ecological sexual dimorphism may play a key role in niche divergence among nascent species and demonstrate that ecological sexual dimorphism and ecological speciation can and do evolve concurrently in the early stages of adaptive radiation.
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spelling pubmed-54339982017-05-17 Disruptive natural selection predicts divergence between the sexes during adaptive radiation De Lisle, Stephen P. Rowe, Locke Ecol Evol Original Research Evolution of sexual dimorphism in ecologically relevant traits, for example, via resource competition between the sexes, is traditionally envisioned to stall the progress of adaptive radiation. An alternative view is that evolution of ecological sexual dimorphism could in fact play an important positive role by facilitating sex‐specific adaptation. How competition‐driven disruptive selection, ecological sexual dimorphism, and speciation interact during real adaptive radiations is thus a critical and open empirical question. Here, we examine the relationships between these three processes in a clade of salamanders that has recently radiated into divergent niches associated with an aquatic life cycle. We find that morphological divergence between the sexes has occurred in a combination of head shape traits that are under disruptive natural selection within breeding ponds, while divergence among species means has occurred independently of this disruptive selection. Further, we find that adaptation to aquatic life is associated with increased sexual dimorphism across taxa, consistent with the hypothesis of clade‐wide character displacement between the sexes. Our results suggest the evolution of ecological sexual dimorphism may play a key role in niche divergence among nascent species and demonstrate that ecological sexual dimorphism and ecological speciation can and do evolve concurrently in the early stages of adaptive radiation. John Wiley and Sons Inc. 2017-04-11 /pmc/articles/PMC5433998/ /pubmed/28515895 http://dx.doi.org/10.1002/ece3.2868 Text en © 2017 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (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 Original Research
De Lisle, Stephen P.
Rowe, Locke
Disruptive natural selection predicts divergence between the sexes during adaptive radiation
title Disruptive natural selection predicts divergence between the sexes during adaptive radiation
title_full Disruptive natural selection predicts divergence between the sexes during adaptive radiation
title_fullStr Disruptive natural selection predicts divergence between the sexes during adaptive radiation
title_full_unstemmed Disruptive natural selection predicts divergence between the sexes during adaptive radiation
title_short Disruptive natural selection predicts divergence between the sexes during adaptive radiation
title_sort disruptive natural selection predicts divergence between the sexes during adaptive radiation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433998/
https://www.ncbi.nlm.nih.gov/pubmed/28515895
http://dx.doi.org/10.1002/ece3.2868
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