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Functional explanation of extreme hatching asynchrony: Male Manipulation Hypothesis
Hatching asynchrony in birds is considered an adaptation to facilitate brood reduction because under conditions of food scarcity, the smallest nestling usually dies soon after hatching, thereby minimizing parental effort. However, in species with extreme hatching asynchrony, the last hatchlings para...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Science Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486522/ https://www.ncbi.nlm.nih.gov/pubmed/36031767 http://dx.doi.org/10.24272/j.issn.2095-8137.2021.455 |
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author | Soler, Manuel Ruiz-Raya, Francisco Sánchez-Pérez, Lucía Ibáñez-Álamo, Juan Diego Soler, Juan José |
author_facet | Soler, Manuel Ruiz-Raya, Francisco Sánchez-Pérez, Lucía Ibáñez-Álamo, Juan Diego Soler, Juan José |
author_sort | Soler, Manuel |
collection | PubMed |
description | Hatching asynchrony in birds is considered an adaptation to facilitate brood reduction because under conditions of food scarcity, the smallest nestling usually dies soon after hatching, thereby minimizing parental effort. However, in species with extreme hatching asynchrony, the last hatchlings paradoxically experience a very low probability of survival and death can take so long that it can hardly be considered an adaptation. Here, we propose and experimentally tested a new adaptive hypothesis explaining the brood reduction paradox, namely the “Male Manipulation Hypothesis”. Our hypothesis suggests that by inducing asynchronous hatching, females increase the feeding requirements of the brood, which will induce males to increase provisioning effort. In addition, females may extend the period of male manipulation by feeding the smallest nestling just enough to sustain life. Our study showed that male common blackbirds (Turdus merula) increased their effort (i.e., number of food items per hour) in experimental asynchronous broods compared to synchronous broods, while females reduced their contribution, as predicted by the hypothesis. |
format | Online Article Text |
id | pubmed-9486522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Science Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94865222022-09-23 Functional explanation of extreme hatching asynchrony: Male Manipulation Hypothesis Soler, Manuel Ruiz-Raya, Francisco Sánchez-Pérez, Lucía Ibáñez-Álamo, Juan Diego Soler, Juan José Zool Res Article Hatching asynchrony in birds is considered an adaptation to facilitate brood reduction because under conditions of food scarcity, the smallest nestling usually dies soon after hatching, thereby minimizing parental effort. However, in species with extreme hatching asynchrony, the last hatchlings paradoxically experience a very low probability of survival and death can take so long that it can hardly be considered an adaptation. Here, we propose and experimentally tested a new adaptive hypothesis explaining the brood reduction paradox, namely the “Male Manipulation Hypothesis”. Our hypothesis suggests that by inducing asynchronous hatching, females increase the feeding requirements of the brood, which will induce males to increase provisioning effort. In addition, females may extend the period of male manipulation by feeding the smallest nestling just enough to sustain life. Our study showed that male common blackbirds (Turdus merula) increased their effort (i.e., number of food items per hour) in experimental asynchronous broods compared to synchronous broods, while females reduced their contribution, as predicted by the hypothesis. Science Press 2022-09-18 /pmc/articles/PMC9486522/ /pubmed/36031767 http://dx.doi.org/10.24272/j.issn.2095-8137.2021.455 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Soler, Manuel Ruiz-Raya, Francisco Sánchez-Pérez, Lucía Ibáñez-Álamo, Juan Diego Soler, Juan José Functional explanation of extreme hatching asynchrony: Male Manipulation Hypothesis |
title | Functional explanation of extreme hatching asynchrony: Male Manipulation Hypothesis |
title_full | Functional explanation of extreme hatching asynchrony: Male Manipulation Hypothesis |
title_fullStr | Functional explanation of extreme hatching asynchrony: Male Manipulation Hypothesis |
title_full_unstemmed | Functional explanation of extreme hatching asynchrony: Male Manipulation Hypothesis |
title_short | Functional explanation of extreme hatching asynchrony: Male Manipulation Hypothesis |
title_sort | functional explanation of extreme hatching asynchrony: male manipulation hypothesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486522/ https://www.ncbi.nlm.nih.gov/pubmed/36031767 http://dx.doi.org/10.24272/j.issn.2095-8137.2021.455 |
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