Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Foster, Susan A., O'Neil, Shannon, King, Richard W., Baker, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2019
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
_version_ 1783394650098237440
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
work_keys_str_mv AT fostersusana replicatedevolutionaryinhibitionofacomplexancestralbehaviourinanadaptiveradiation
AT oneilshannon replicatedevolutionaryinhibitionofacomplexancestralbehaviourinanadaptiveradiation
AT kingrichardw replicatedevolutionaryinhibitionofacomplexancestralbehaviourinanadaptiveradiation
AT bakerjohna replicatedevolutionaryinhibitionofacomplexancestralbehaviourinanadaptiveradiation