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Rapid morphological divergence following a human-mediated introduction: the role of drift and directional selection

Theory predicts that when populations are established by few individuals, random founder effects can facilitate rapid phenotypic divergence even in the absence of selective processes. However, empirical evidence from historically documented colonisations suggest that, in most cases, drift alone is n...

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Autores principales: Sendell-Price, Ashley T., Ruegg, Kristen C., Clegg, Sonya. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080774/
https://www.ncbi.nlm.nih.gov/pubmed/32080374
http://dx.doi.org/10.1038/s41437-020-0298-8
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author Sendell-Price, Ashley T.
Ruegg, Kristen C.
Clegg, Sonya. M.
author_facet Sendell-Price, Ashley T.
Ruegg, Kristen C.
Clegg, Sonya. M.
author_sort Sendell-Price, Ashley T.
collection PubMed
description Theory predicts that when populations are established by few individuals, random founder effects can facilitate rapid phenotypic divergence even in the absence of selective processes. However, empirical evidence from historically documented colonisations suggest that, in most cases, drift alone is not sufficient to explain the rate of morphological divergence. Here, using the human-mediated introduction of the silvereye (Zosterops lateralis) to French Polynesia, which represents a potentially extreme example of population founding, we reassess the potential for morphological shifts to arise via drift alone. Despite only 80 years of separation from their New Zealand ancestors, French Polynesian silvereyes displayed significant changes in body and bill size and shape, most of which could be accounted for by drift, without the need to invoke selection. However, signatures of selection at genes previously identified as candidates for bill size and body shape differences in a range of bird species, also suggests a role for selective processes in driving morphological shifts within this population. Twenty-four SNPs in our RAD-Seq dataset were also found to be strongly associated with phenotypic variation. Hence, even under population founding extremes, when it is difficult to reject drift as the sole mechanism based on rate tests of phenotypic shifts, the additional role of divergent natural selection in novel environments can be revealed at the level of the genome.
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spelling pubmed-70807742020-03-19 Rapid morphological divergence following a human-mediated introduction: the role of drift and directional selection Sendell-Price, Ashley T. Ruegg, Kristen C. Clegg, Sonya. M. Heredity (Edinb) Article Theory predicts that when populations are established by few individuals, random founder effects can facilitate rapid phenotypic divergence even in the absence of selective processes. However, empirical evidence from historically documented colonisations suggest that, in most cases, drift alone is not sufficient to explain the rate of morphological divergence. Here, using the human-mediated introduction of the silvereye (Zosterops lateralis) to French Polynesia, which represents a potentially extreme example of population founding, we reassess the potential for morphological shifts to arise via drift alone. Despite only 80 years of separation from their New Zealand ancestors, French Polynesian silvereyes displayed significant changes in body and bill size and shape, most of which could be accounted for by drift, without the need to invoke selection. However, signatures of selection at genes previously identified as candidates for bill size and body shape differences in a range of bird species, also suggests a role for selective processes in driving morphological shifts within this population. Twenty-four SNPs in our RAD-Seq dataset were also found to be strongly associated with phenotypic variation. Hence, even under population founding extremes, when it is difficult to reject drift as the sole mechanism based on rate tests of phenotypic shifts, the additional role of divergent natural selection in novel environments can be revealed at the level of the genome. Springer International Publishing 2020-02-20 2020-04 /pmc/articles/PMC7080774/ /pubmed/32080374 http://dx.doi.org/10.1038/s41437-020-0298-8 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sendell-Price, Ashley T.
Ruegg, Kristen C.
Clegg, Sonya. M.
Rapid morphological divergence following a human-mediated introduction: the role of drift and directional selection
title Rapid morphological divergence following a human-mediated introduction: the role of drift and directional selection
title_full Rapid morphological divergence following a human-mediated introduction: the role of drift and directional selection
title_fullStr Rapid morphological divergence following a human-mediated introduction: the role of drift and directional selection
title_full_unstemmed Rapid morphological divergence following a human-mediated introduction: the role of drift and directional selection
title_short Rapid morphological divergence following a human-mediated introduction: the role of drift and directional selection
title_sort rapid morphological divergence following a human-mediated introduction: the role of drift and directional selection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080774/
https://www.ncbi.nlm.nih.gov/pubmed/32080374
http://dx.doi.org/10.1038/s41437-020-0298-8
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