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How conflict shapes evolution in poeciliid fishes

In live-bearing animal lineages, the evolution of the placenta is predicted to create an arena for genomic conflict during pregnancy, drive patterns of male sexual selection, and increase the rate of speciation. Here we test these predictions of the viviparity driven conflict hypothesis (VDCH) in li...

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Autores principales: Furness, Andrew I., Pollux, Bart J. A., Meredith, Robert W., Springer, Mark S., Reznick, David N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659687/
https://www.ncbi.nlm.nih.gov/pubmed/31350395
http://dx.doi.org/10.1038/s41467-019-11307-5
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author Furness, Andrew I.
Pollux, Bart J. A.
Meredith, Robert W.
Springer, Mark S.
Reznick, David N.
author_facet Furness, Andrew I.
Pollux, Bart J. A.
Meredith, Robert W.
Springer, Mark S.
Reznick, David N.
author_sort Furness, Andrew I.
collection PubMed
description In live-bearing animal lineages, the evolution of the placenta is predicted to create an arena for genomic conflict during pregnancy, drive patterns of male sexual selection, and increase the rate of speciation. Here we test these predictions of the viviparity driven conflict hypothesis (VDCH) in live-bearing poecilid fishes, a group showing multiple independent origins of placentation and extreme variation in male sexually selected traits. As predicted, male sexually selected traits are only gained in lineages that lack placentas; while there is little or no influence of male traits on the evolution of placentas. Both results are consistent with the mode of female provisioning governing the evolution of male attributes. Moreover, it is the presence of male sexually selected traits (pre-copulatory), rather than placentation (post-copulatory), that are associated with higher rates of speciation. These results highlight a causal interaction between female reproductive mode, male sexual selection and the rate of speciation, suggesting a role for conflict in shaping diverse aspects of organismal biology.
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spelling pubmed-66596872019-07-29 How conflict shapes evolution in poeciliid fishes Furness, Andrew I. Pollux, Bart J. A. Meredith, Robert W. Springer, Mark S. Reznick, David N. Nat Commun Article In live-bearing animal lineages, the evolution of the placenta is predicted to create an arena for genomic conflict during pregnancy, drive patterns of male sexual selection, and increase the rate of speciation. Here we test these predictions of the viviparity driven conflict hypothesis (VDCH) in live-bearing poecilid fishes, a group showing multiple independent origins of placentation and extreme variation in male sexually selected traits. As predicted, male sexually selected traits are only gained in lineages that lack placentas; while there is little or no influence of male traits on the evolution of placentas. Both results are consistent with the mode of female provisioning governing the evolution of male attributes. Moreover, it is the presence of male sexually selected traits (pre-copulatory), rather than placentation (post-copulatory), that are associated with higher rates of speciation. These results highlight a causal interaction between female reproductive mode, male sexual selection and the rate of speciation, suggesting a role for conflict in shaping diverse aspects of organismal biology. Nature Publishing Group UK 2019-07-26 /pmc/articles/PMC6659687/ /pubmed/31350395 http://dx.doi.org/10.1038/s41467-019-11307-5 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
Furness, Andrew I.
Pollux, Bart J. A.
Meredith, Robert W.
Springer, Mark S.
Reznick, David N.
How conflict shapes evolution in poeciliid fishes
title How conflict shapes evolution in poeciliid fishes
title_full How conflict shapes evolution in poeciliid fishes
title_fullStr How conflict shapes evolution in poeciliid fishes
title_full_unstemmed How conflict shapes evolution in poeciliid fishes
title_short How conflict shapes evolution in poeciliid fishes
title_sort how conflict shapes evolution in poeciliid fishes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659687/
https://www.ncbi.nlm.nih.gov/pubmed/31350395
http://dx.doi.org/10.1038/s41467-019-11307-5
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