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How does male–male competition generate negative frequency-dependent selection and disruptive selection during speciation?

Natural selection has been shown to drive population differentiation and speciation. The role of sexual selection in this process is controversial; however, most of the work has centered on mate choice while the role of male–male competition in speciation is relatively understudied. Here, we outline...

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Autores principales: Dijkstra, Peter D, Border, Shana E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809039/
https://www.ncbi.nlm.nih.gov/pubmed/29492042
http://dx.doi.org/10.1093/cz/zox079
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author Dijkstra, Peter D
Border, Shana E
author_facet Dijkstra, Peter D
Border, Shana E
author_sort Dijkstra, Peter D
collection PubMed
description Natural selection has been shown to drive population differentiation and speciation. The role of sexual selection in this process is controversial; however, most of the work has centered on mate choice while the role of male–male competition in speciation is relatively understudied. Here, we outline how male–male competition can be a source of diversifying selection on male competitive phenotypes, and how this can contribute to the evolution of reproductive isolation. We highlight how negative frequency-dependent selection (advantage of rare phenotype arising from stronger male–male competition between similar male phenotypes compared with dissimilar male phenotypes) and disruptive selection (advantage of extreme phenotypes) drives the evolution of diversity in competitive traits such as weapon size, nuptial coloration, or aggressiveness. We underscore that male–male competition interacts with other life-history functions and that variable male competitive phenotypes may represent alternative adaptive options. In addition to competition for mates, aggressive interference competition for ecological resources can exert selection on competitor signals. We call for a better integration of male–male competition with ecological interference competition since both can influence the process of speciation via comparable but distinct mechanisms. Altogether, we present a more comprehensive framework for studying the role of male–male competition in speciation, and emphasize the need for better integration of insights gained from other fields studying the evolutionary, behavioral, and physiological consequences of agonistic interactions.
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spelling pubmed-58090392018-02-28 How does male–male competition generate negative frequency-dependent selection and disruptive selection during speciation? Dijkstra, Peter D Border, Shana E Curr Zool Special Column: Male Competition and Speciation Natural selection has been shown to drive population differentiation and speciation. The role of sexual selection in this process is controversial; however, most of the work has centered on mate choice while the role of male–male competition in speciation is relatively understudied. Here, we outline how male–male competition can be a source of diversifying selection on male competitive phenotypes, and how this can contribute to the evolution of reproductive isolation. We highlight how negative frequency-dependent selection (advantage of rare phenotype arising from stronger male–male competition between similar male phenotypes compared with dissimilar male phenotypes) and disruptive selection (advantage of extreme phenotypes) drives the evolution of diversity in competitive traits such as weapon size, nuptial coloration, or aggressiveness. We underscore that male–male competition interacts with other life-history functions and that variable male competitive phenotypes may represent alternative adaptive options. In addition to competition for mates, aggressive interference competition for ecological resources can exert selection on competitor signals. We call for a better integration of male–male competition with ecological interference competition since both can influence the process of speciation via comparable but distinct mechanisms. Altogether, we present a more comprehensive framework for studying the role of male–male competition in speciation, and emphasize the need for better integration of insights gained from other fields studying the evolutionary, behavioral, and physiological consequences of agonistic interactions. Oxford University Press 2018-02 2018-01-02 /pmc/articles/PMC5809039/ /pubmed/29492042 http://dx.doi.org/10.1093/cz/zox079 Text en © The Author(s) (2018). Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Special Column: Male Competition and Speciation
Dijkstra, Peter D
Border, Shana E
How does male–male competition generate negative frequency-dependent selection and disruptive selection during speciation?
title How does male–male competition generate negative frequency-dependent selection and disruptive selection during speciation?
title_full How does male–male competition generate negative frequency-dependent selection and disruptive selection during speciation?
title_fullStr How does male–male competition generate negative frequency-dependent selection and disruptive selection during speciation?
title_full_unstemmed How does male–male competition generate negative frequency-dependent selection and disruptive selection during speciation?
title_short How does male–male competition generate negative frequency-dependent selection and disruptive selection during speciation?
title_sort how does male–male competition generate negative frequency-dependent selection and disruptive selection during speciation?
topic Special Column: Male Competition and Speciation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809039/
https://www.ncbi.nlm.nih.gov/pubmed/29492042
http://dx.doi.org/10.1093/cz/zox079
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