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Coevolution between Himalayan cuckoos and 2 sympatric Pycnonotidae hosts
Selection due to cuckoo parasitism is responsible for the evolution of anti-parasitism defenses in hosts. Different host species breeding sympatrically with a single parasitic cuckoo may evolve different strategies to reduce the risk of counter cuckoo parasitism, resulting in different interactions...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599071/ https://www.ncbi.nlm.nih.gov/pubmed/34805541 http://dx.doi.org/10.1093/cz/zoab073 |
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author | Yang, Canchao Li, Qihong Su, Tongping Møller, Anders Pape Liang, Wei |
author_facet | Yang, Canchao Li, Qihong Su, Tongping Møller, Anders Pape Liang, Wei |
author_sort | Yang, Canchao |
collection | PubMed |
description | Selection due to cuckoo parasitism is responsible for the evolution of anti-parasitism defenses in hosts. Different host species breeding sympatrically with a single parasitic cuckoo may evolve different strategies to reduce the risk of counter cuckoo parasitism, resulting in different interactions between cuckoos and hosts in areas of sympatry. Here, we studied the coevolutionary interactions between Himalayan cuckoos Cuculus saturatus and 2 sympatric and closely related potential hosts belonging to the family Pycnonotidae, the brown-breasted bulbul Pycnonotus xanthorrhous and the collared finchbill Spizixos semitorques. We investigated parasitism rates and nest-site selection (nest height, nest cover, human disturbance, perch height, forest distance, and degree of concealment) related to parasitism risk, nest defense against a cuckoo dummy, and egg rejection against cuckoo model eggs. Bulbuls used specific nest sites that were further away from forests than those of finchbills, and they behaved more aggressively toward cuckoos than finchbills. In contrast, bulbuls possessed moderate egg rejection ability, whereas the finchbill rejected 100% of cuckoo model eggs. We suggest that selection of a nest site away from forests by the bulbul explains the absence of parasitism by Himalayan cuckoos. We suggest that these interspecific differences in nest-site selection and nest defense indicate alternative responses to selection due to cuckoos. |
format | Online Article Text |
id | pubmed-8599071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85990712021-11-18 Coevolution between Himalayan cuckoos and 2 sympatric Pycnonotidae hosts Yang, Canchao Li, Qihong Su, Tongping Møller, Anders Pape Liang, Wei Curr Zool Special Column: Avian brood parasite/host interactions: behavior, personality and mechanism Selection due to cuckoo parasitism is responsible for the evolution of anti-parasitism defenses in hosts. Different host species breeding sympatrically with a single parasitic cuckoo may evolve different strategies to reduce the risk of counter cuckoo parasitism, resulting in different interactions between cuckoos and hosts in areas of sympatry. Here, we studied the coevolutionary interactions between Himalayan cuckoos Cuculus saturatus and 2 sympatric and closely related potential hosts belonging to the family Pycnonotidae, the brown-breasted bulbul Pycnonotus xanthorrhous and the collared finchbill Spizixos semitorques. We investigated parasitism rates and nest-site selection (nest height, nest cover, human disturbance, perch height, forest distance, and degree of concealment) related to parasitism risk, nest defense against a cuckoo dummy, and egg rejection against cuckoo model eggs. Bulbuls used specific nest sites that were further away from forests than those of finchbills, and they behaved more aggressively toward cuckoos than finchbills. In contrast, bulbuls possessed moderate egg rejection ability, whereas the finchbill rejected 100% of cuckoo model eggs. We suggest that selection of a nest site away from forests by the bulbul explains the absence of parasitism by Himalayan cuckoos. We suggest that these interspecific differences in nest-site selection and nest defense indicate alternative responses to selection due to cuckoos. Oxford University Press 2021-09-01 /pmc/articles/PMC8599071/ /pubmed/34805541 http://dx.doi.org/10.1093/cz/zoab073 Text en © The Author(s) (2021). Published by Oxford University Press on behalf of Editorial Office, Current Zoology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Special Column: Avian brood parasite/host interactions: behavior, personality and mechanism Yang, Canchao Li, Qihong Su, Tongping Møller, Anders Pape Liang, Wei Coevolution between Himalayan cuckoos and 2 sympatric Pycnonotidae hosts |
title | Coevolution between Himalayan cuckoos and 2 sympatric Pycnonotidae hosts |
title_full | Coevolution between Himalayan cuckoos and 2 sympatric Pycnonotidae hosts |
title_fullStr | Coevolution between Himalayan cuckoos and 2 sympatric Pycnonotidae hosts |
title_full_unstemmed | Coevolution between Himalayan cuckoos and 2 sympatric Pycnonotidae hosts |
title_short | Coevolution between Himalayan cuckoos and 2 sympatric Pycnonotidae hosts |
title_sort | coevolution between himalayan cuckoos and 2 sympatric pycnonotidae hosts |
topic | Special Column: Avian brood parasite/host interactions: behavior, personality and mechanism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599071/ https://www.ncbi.nlm.nih.gov/pubmed/34805541 http://dx.doi.org/10.1093/cz/zoab073 |
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