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Replicated evolutionary inhibition of a complex ancestral behaviour in an adaptive radiation
Adaptive radiations often exhibit high levels of phenotypic replication, a phenomenon that can be explained by selection on standing variation in repeatedly divergent environments or by the influence of ancestral plasticity on selection in divergent environments. Here, we offer the first evidence th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371902/ https://www.ncbi.nlm.nih.gov/pubmed/30958220 http://dx.doi.org/10.1098/rsbl.2018.0647 |
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author | Foster, Susan A. O'Neil, Shannon King, Richard W. Baker, John A. |
author_facet | Foster, Susan A. O'Neil, Shannon King, Richard W. Baker, John A. |
author_sort | Foster, Susan A. |
collection | PubMed |
description | Adaptive radiations often exhibit high levels of phenotypic replication, a phenomenon that can be explained by selection on standing variation in repeatedly divergent environments or by the influence of ancestral plasticity on selection in divergent environments. Here, we offer the first evidence that plastic loss of expression of a complex display in a novel environment, followed by selection against expression, could lead to replicated evolutionary inhibition of the phenotype. In both ancestral (oceanic) and benthic (freshwater) populations of the threespine stickleback fish, cannibalism is common and males defending nests respond to approaching groups with a complex diversionary display. This display is not exhibited by males in allopatric, limnetic (freshwater) populations from which cannibalistic groups are absent. Laboratory-reared males from three limnetic populations exhibit a reduced tendency to respond to cannibalistic foraging groups relative to laboratory-reared ancestral and benthic males, but still are capable of producing a similar array of forms of the display despite many generations of disuse. Thus, replication in adaptive radiations can reflect reduced expression of an ancestral trait followed by evolutionary inhibition while the population retains the capacity to express the trait under extreme ancestral conditions. |
format | Online Article Text |
id | pubmed-6371902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-63719022019-02-26 Replicated evolutionary inhibition of a complex ancestral behaviour in an adaptive radiation Foster, Susan A. O'Neil, Shannon King, Richard W. Baker, John A. Biol Lett Evolutionary Biology Adaptive radiations often exhibit high levels of phenotypic replication, a phenomenon that can be explained by selection on standing variation in repeatedly divergent environments or by the influence of ancestral plasticity on selection in divergent environments. Here, we offer the first evidence that plastic loss of expression of a complex display in a novel environment, followed by selection against expression, could lead to replicated evolutionary inhibition of the phenotype. In both ancestral (oceanic) and benthic (freshwater) populations of the threespine stickleback fish, cannibalism is common and males defending nests respond to approaching groups with a complex diversionary display. This display is not exhibited by males in allopatric, limnetic (freshwater) populations from which cannibalistic groups are absent. Laboratory-reared males from three limnetic populations exhibit a reduced tendency to respond to cannibalistic foraging groups relative to laboratory-reared ancestral and benthic males, but still are capable of producing a similar array of forms of the display despite many generations of disuse. Thus, replication in adaptive radiations can reflect reduced expression of an ancestral trait followed by evolutionary inhibition while the population retains the capacity to express the trait under extreme ancestral conditions. The Royal Society 2019-01 2019-01-30 /pmc/articles/PMC6371902/ /pubmed/30958220 http://dx.doi.org/10.1098/rsbl.2018.0647 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolutionary Biology Foster, Susan A. O'Neil, Shannon King, Richard W. Baker, John A. Replicated evolutionary inhibition of a complex ancestral behaviour in an adaptive radiation |
title | Replicated evolutionary inhibition of a complex ancestral behaviour in an adaptive radiation |
title_full | Replicated evolutionary inhibition of a complex ancestral behaviour in an adaptive radiation |
title_fullStr | Replicated evolutionary inhibition of a complex ancestral behaviour in an adaptive radiation |
title_full_unstemmed | Replicated evolutionary inhibition of a complex ancestral behaviour in an adaptive radiation |
title_short | Replicated evolutionary inhibition of a complex ancestral behaviour in an adaptive radiation |
title_sort | replicated evolutionary inhibition of a complex ancestral behaviour in an adaptive radiation |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371902/ https://www.ncbi.nlm.nih.gov/pubmed/30958220 http://dx.doi.org/10.1098/rsbl.2018.0647 |
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