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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...

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Autores principales: Soler, Manuel, Ruiz-Raya, Francisco, Sánchez-Pérez, Lucía, Ibáñez-Álamo, Juan Diego, Soler, Juan José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Science Press 2022
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.
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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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