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Evolutionary significance of antiparasite, antipredator and learning phenotypes of avian nest defence

Avian nest defence, which is expected to serve both antiparasite and antipredator functions, may benefit or be detrimental to birds, although selective forces that potentially operate on nest defence have not been quantified as a whole. Together with fitness values, we analysed two traits of nest de...

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Autores principales: Campobello, Daniela, Sealy, Spencer G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043525/
https://www.ncbi.nlm.nih.gov/pubmed/30002381
http://dx.doi.org/10.1038/s41598-018-28275-3
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author Campobello, Daniela
Sealy, Spencer G.
author_facet Campobello, Daniela
Sealy, Spencer G.
author_sort Campobello, Daniela
collection PubMed
description Avian nest defence, which is expected to serve both antiparasite and antipredator functions, may benefit or be detrimental to birds, although selective forces that potentially operate on nest defence have not been quantified as a whole. Together with fitness values, we analysed two traits of nest defence, intensity and plasticity, in two distantly related passerine species, yellow warbler (Setophaga petechia) in North America and reed warbler (Acrocephalus scirpaceus) in Europe, both favourite host species for brood parasites. Breeders that escaped parasitism were the most vocal among reed warblers, whereas there was no specific defence phenotype that predicted prevention of parasitism in yellow warblers. Breeders that escaped nest predation were, in both species, those with the most distractive response at the first exposure to a nest-threatening event, such as the experimental predation or parasitism simulated at the nest. However, increasing defence intensity benefited yellow warblers but was detrimental to reed warblers, because intense defence responses attracted predators. Adaptiveness of nest defence was revealed by nest defence phenotypes when examined in concert with the seasonal fitness (i.e. measures of reproductive success). Results revealed selective forces favoured yellow warblers with strong defence phenotypes. Opposite forces were instead revealed among reed warblers whose favoured phenotypes were strong, yet less flexible, defenders.
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spelling pubmed-60435252018-07-15 Evolutionary significance of antiparasite, antipredator and learning phenotypes of avian nest defence Campobello, Daniela Sealy, Spencer G. Sci Rep Article Avian nest defence, which is expected to serve both antiparasite and antipredator functions, may benefit or be detrimental to birds, although selective forces that potentially operate on nest defence have not been quantified as a whole. Together with fitness values, we analysed two traits of nest defence, intensity and plasticity, in two distantly related passerine species, yellow warbler (Setophaga petechia) in North America and reed warbler (Acrocephalus scirpaceus) in Europe, both favourite host species for brood parasites. Breeders that escaped parasitism were the most vocal among reed warblers, whereas there was no specific defence phenotype that predicted prevention of parasitism in yellow warblers. Breeders that escaped nest predation were, in both species, those with the most distractive response at the first exposure to a nest-threatening event, such as the experimental predation or parasitism simulated at the nest. However, increasing defence intensity benefited yellow warblers but was detrimental to reed warblers, because intense defence responses attracted predators. Adaptiveness of nest defence was revealed by nest defence phenotypes when examined in concert with the seasonal fitness (i.e. measures of reproductive success). Results revealed selective forces favoured yellow warblers with strong defence phenotypes. Opposite forces were instead revealed among reed warblers whose favoured phenotypes were strong, yet less flexible, defenders. Nature Publishing Group UK 2018-07-12 /pmc/articles/PMC6043525/ /pubmed/30002381 http://dx.doi.org/10.1038/s41598-018-28275-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Campobello, Daniela
Sealy, Spencer G.
Evolutionary significance of antiparasite, antipredator and learning phenotypes of avian nest defence
title Evolutionary significance of antiparasite, antipredator and learning phenotypes of avian nest defence
title_full Evolutionary significance of antiparasite, antipredator and learning phenotypes of avian nest defence
title_fullStr Evolutionary significance of antiparasite, antipredator and learning phenotypes of avian nest defence
title_full_unstemmed Evolutionary significance of antiparasite, antipredator and learning phenotypes of avian nest defence
title_short Evolutionary significance of antiparasite, antipredator and learning phenotypes of avian nest defence
title_sort evolutionary significance of antiparasite, antipredator and learning phenotypes of avian nest defence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043525/
https://www.ncbi.nlm.nih.gov/pubmed/30002381
http://dx.doi.org/10.1038/s41598-018-28275-3
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