Cargando…
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...
Autores principales: | , |
---|---|
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 |
_version_ | 1782213463322394624 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3189372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT spottiswoodeclairen howtoevadeacoevolvingbroodparasiteeggdiscriminationversuseggvariabilityashostdefences AT stevensmartin howtoevadeacoevolvingbroodparasiteeggdiscriminationversuseggvariabilityashostdefences |