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Coevolution in Action: Disruptive Selection on Egg Colour in an Avian Brood Parasite and Its Host

BACKGROUND: Trait polymorphism can evolve as a consequence of frequency-dependent selection. Coevolutionary interactions between hosts and parasites may lead to selection on both to evolve extreme phenotypes deviating from the norm, through disruptive selection. METHODOLOGY/PRINCIPAL FINDING: Here,...

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Autores principales: Yang, Canchao, Liang, Wei, Cai, Yan, Shi, Suhua, Takasu, Fugo, Møller, Anders P., Antonov, Anton, Fossøy, Frode, Moksnes, Arne, Røskaft, Eivin, Stokke, Bård G.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877083/
https://www.ncbi.nlm.nih.gov/pubmed/20520815
http://dx.doi.org/10.1371/journal.pone.0010816
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author Yang, Canchao
Liang, Wei
Cai, Yan
Shi, Suhua
Takasu, Fugo
Møller, Anders P.
Antonov, Anton
Fossøy, Frode
Moksnes, Arne
Røskaft, Eivin
Stokke, Bård G.
author_facet Yang, Canchao
Liang, Wei
Cai, Yan
Shi, Suhua
Takasu, Fugo
Møller, Anders P.
Antonov, Anton
Fossøy, Frode
Moksnes, Arne
Røskaft, Eivin
Stokke, Bård G.
author_sort Yang, Canchao
collection PubMed
description BACKGROUND: Trait polymorphism can evolve as a consequence of frequency-dependent selection. Coevolutionary interactions between hosts and parasites may lead to selection on both to evolve extreme phenotypes deviating from the norm, through disruptive selection. METHODOLOGY/PRINCIPAL FINDING: Here, we show through detailed field studies and experimental procedures that the ashy-throated parrotbill (Paradoxornis alphonsianus) and its avian brood parasite, the common cuckoo (Cuculus canorus), have both evolved egg polymorphism manifested in discrete immaculate white, pale blue, and blue egg phenotypes within a single population. In this host-parasite system the most common egg colours were white and blue, with no significant difference in parasitism rates between hosts laying eggs of either colour. Furthermore, selection on parasites for countering the evolution of host egg types appears to be strong, since ashy-throated parrotbills have evolved rejection abilities for even partially mimetic eggs. CONCLUSIONS/SIGNIFICANCE: The parrotbill-cuckoo system constitutes a clear outcome of disruptive selection on both host and parasite egg phenotypes driven by coevolution, due to the cost of parasitism in the host and by host defences in the parasite. The present study is to our knowledge the first to report the influence of disruptive selection on evolution of discrete phenotypes in both parasite and host traits in an avian brood parasitism system.
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spelling pubmed-28770832010-06-02 Coevolution in Action: Disruptive Selection on Egg Colour in an Avian Brood Parasite and Its Host Yang, Canchao Liang, Wei Cai, Yan Shi, Suhua Takasu, Fugo Møller, Anders P. Antonov, Anton Fossøy, Frode Moksnes, Arne Røskaft, Eivin Stokke, Bård G. PLoS One Research Article BACKGROUND: Trait polymorphism can evolve as a consequence of frequency-dependent selection. Coevolutionary interactions between hosts and parasites may lead to selection on both to evolve extreme phenotypes deviating from the norm, through disruptive selection. METHODOLOGY/PRINCIPAL FINDING: Here, we show through detailed field studies and experimental procedures that the ashy-throated parrotbill (Paradoxornis alphonsianus) and its avian brood parasite, the common cuckoo (Cuculus canorus), have both evolved egg polymorphism manifested in discrete immaculate white, pale blue, and blue egg phenotypes within a single population. In this host-parasite system the most common egg colours were white and blue, with no significant difference in parasitism rates between hosts laying eggs of either colour. Furthermore, selection on parasites for countering the evolution of host egg types appears to be strong, since ashy-throated parrotbills have evolved rejection abilities for even partially mimetic eggs. CONCLUSIONS/SIGNIFICANCE: The parrotbill-cuckoo system constitutes a clear outcome of disruptive selection on both host and parasite egg phenotypes driven by coevolution, due to the cost of parasitism in the host and by host defences in the parasite. The present study is to our knowledge the first to report the influence of disruptive selection on evolution of discrete phenotypes in both parasite and host traits in an avian brood parasitism system. Public Library of Science 2010-05-26 /pmc/articles/PMC2877083/ /pubmed/20520815 http://dx.doi.org/10.1371/journal.pone.0010816 Text en Yang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yang, Canchao
Liang, Wei
Cai, Yan
Shi, Suhua
Takasu, Fugo
Møller, Anders P.
Antonov, Anton
Fossøy, Frode
Moksnes, Arne
Røskaft, Eivin
Stokke, Bård G.
Coevolution in Action: Disruptive Selection on Egg Colour in an Avian Brood Parasite and Its Host
title Coevolution in Action: Disruptive Selection on Egg Colour in an Avian Brood Parasite and Its Host
title_full Coevolution in Action: Disruptive Selection on Egg Colour in an Avian Brood Parasite and Its Host
title_fullStr Coevolution in Action: Disruptive Selection on Egg Colour in an Avian Brood Parasite and Its Host
title_full_unstemmed Coevolution in Action: Disruptive Selection on Egg Colour in an Avian Brood Parasite and Its Host
title_short Coevolution in Action: Disruptive Selection on Egg Colour in an Avian Brood Parasite and Its Host
title_sort coevolution in action: disruptive selection on egg colour in an avian brood parasite and its host
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877083/
https://www.ncbi.nlm.nih.gov/pubmed/20520815
http://dx.doi.org/10.1371/journal.pone.0010816
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