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How to evade a coevolving brood parasite: egg discrimination versus egg variability as host defences

Arms races between avian brood parasites and their hosts often result in parasitic mimicry of host eggs, to evade rejection. Once egg mimicry has evolved, host defences could escalate in two ways: (i) hosts could improve their level of egg discrimination; and (ii) negative frequency-dependent select...

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Autores principales: Spottiswoode, Claire N., Stevens, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189372/
https://www.ncbi.nlm.nih.gov/pubmed/21490019
http://dx.doi.org/10.1098/rspb.2011.0401
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author Spottiswoode, Claire N.
Stevens, Martin
author_facet Spottiswoode, Claire N.
Stevens, Martin
author_sort Spottiswoode, Claire N.
collection PubMed
description Arms races between avian brood parasites and their hosts often result in parasitic mimicry of host eggs, to evade rejection. Once egg mimicry has evolved, host defences could escalate in two ways: (i) hosts could improve their level of egg discrimination; and (ii) negative frequency-dependent selection could generate increased variation in egg appearance (polymorphism) among individuals. Proficiency in one defence might reduce selection on the other, while a combination of the two should enable successful rejection of parasitic eggs. We compared three highly variable host species of the Afrotropical cuckoo finch Anomalospiza imberbis, using egg rejection experiments and modelling of avian colour and pattern vision. We show that each differed in their level of polymorphism, in the visual cues they used to reject foreign eggs, and in their degree of discrimination. The most polymorphic host had the crudest discrimination, whereas the least polymorphic was most discriminating. The third species, not currently parasitized, was intermediate for both defences. A model simulating parasitic laying and host rejection behaviour based on the field experiments showed that the two host strategies result in approximately the same fitness advantage to hosts. Thus, neither strategy is superior, but rather they reflect alternative potential evolutionary trajectories.
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spelling pubmed-31893722011-10-17 How to evade a coevolving brood parasite: egg discrimination versus egg variability as host defences Spottiswoode, Claire N. Stevens, Martin Proc Biol Sci Research Articles Arms races between avian brood parasites and their hosts often result in parasitic mimicry of host eggs, to evade rejection. Once egg mimicry has evolved, host defences could escalate in two ways: (i) hosts could improve their level of egg discrimination; and (ii) negative frequency-dependent selection could generate increased variation in egg appearance (polymorphism) among individuals. Proficiency in one defence might reduce selection on the other, while a combination of the two should enable successful rejection of parasitic eggs. We compared three highly variable host species of the Afrotropical cuckoo finch Anomalospiza imberbis, using egg rejection experiments and modelling of avian colour and pattern vision. We show that each differed in their level of polymorphism, in the visual cues they used to reject foreign eggs, and in their degree of discrimination. The most polymorphic host had the crudest discrimination, whereas the least polymorphic was most discriminating. The third species, not currently parasitized, was intermediate for both defences. A model simulating parasitic laying and host rejection behaviour based on the field experiments showed that the two host strategies result in approximately the same fitness advantage to hosts. Thus, neither strategy is superior, but rather they reflect alternative potential evolutionary trajectories. The Royal Society 2011-12-07 2011-04-13 /pmc/articles/PMC3189372/ /pubmed/21490019 http://dx.doi.org/10.1098/rspb.2011.0401 Text en This journal is © 2011 The Royal Society http://creativecommons.org/licenses/by/3.0/ 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 work is properly cited.
spellingShingle Research Articles
Spottiswoode, Claire N.
Stevens, Martin
How to evade a coevolving brood parasite: egg discrimination versus egg variability as host defences
title How to evade a coevolving brood parasite: egg discrimination versus egg variability as host defences
title_full How to evade a coevolving brood parasite: egg discrimination versus egg variability as host defences
title_fullStr How to evade a coevolving brood parasite: egg discrimination versus egg variability as host defences
title_full_unstemmed How to evade a coevolving brood parasite: egg discrimination versus egg variability as host defences
title_short How to evade a coevolving brood parasite: egg discrimination versus egg variability as host defences
title_sort how to evade a coevolving brood parasite: egg discrimination versus egg variability as host defences
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189372/
https://www.ncbi.nlm.nih.gov/pubmed/21490019
http://dx.doi.org/10.1098/rspb.2011.0401
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