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Vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird

Animals thriving in hot deserts rely on extraordinary adaptations and thermoregulatory capacities to cope with heat. Uncovering such adaptations, and how they may be favoured by selection, is essential for predicting climate change impacts. Recently, the arid-adapted zebra finch was discovered to pr...

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Autores principales: Pessato, Anaïs, McKechnie, Andrew E., Buchanan, Katherine L., Mariette, Mylene M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609653/
https://www.ncbi.nlm.nih.gov/pubmed/33144650
http://dx.doi.org/10.1038/s41598-020-75909-6
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author Pessato, Anaïs
McKechnie, Andrew E.
Buchanan, Katherine L.
Mariette, Mylene M.
author_facet Pessato, Anaïs
McKechnie, Andrew E.
Buchanan, Katherine L.
Mariette, Mylene M.
author_sort Pessato, Anaïs
collection PubMed
description Animals thriving in hot deserts rely on extraordinary adaptations and thermoregulatory capacities to cope with heat. Uncovering such adaptations, and how they may be favoured by selection, is essential for predicting climate change impacts. Recently, the arid-adapted zebra finch was discovered to program their offspring’s development for heat, by producing ‘heat-calls’ during incubation in hot conditions. Intriguingly, heat-calls always occur during panting; and, strikingly, avian evaporative cooling mechanisms typically involve vibrating an element of the respiratory tract, which could conceivably produce sound. Therefore, we tested whether heat-call emission results from a particular thermoregulatory mechanism increasing the parent’s heat tolerance. We repeatedly measured resting metabolic rate, evaporative water loss (EWL) and heat tolerance in adult wild-derived captive zebra finches (n = 44) at increasing air temperatures up to 44 °C. We found high within-individual repeatability in thermoregulatory patterns, with heat-calling triggered at an individual-specific stage of panting. As expected for thermoregulatory mechanisms, both silent panting and heat-calling significantly increased EWL. However, only heat-calling resulted in greater heat tolerance, demonstrating that “vocal panting” brings a thermoregulatory benefit to the emitter. Our findings therefore not only improve our understanding of the evolution of passerine thermal adaptations, but also highlight a novel evolutionary precursor for acoustic signals.
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spelling pubmed-76096532020-11-05 Vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird Pessato, Anaïs McKechnie, Andrew E. Buchanan, Katherine L. Mariette, Mylene M. Sci Rep Article Animals thriving in hot deserts rely on extraordinary adaptations and thermoregulatory capacities to cope with heat. Uncovering such adaptations, and how they may be favoured by selection, is essential for predicting climate change impacts. Recently, the arid-adapted zebra finch was discovered to program their offspring’s development for heat, by producing ‘heat-calls’ during incubation in hot conditions. Intriguingly, heat-calls always occur during panting; and, strikingly, avian evaporative cooling mechanisms typically involve vibrating an element of the respiratory tract, which could conceivably produce sound. Therefore, we tested whether heat-call emission results from a particular thermoregulatory mechanism increasing the parent’s heat tolerance. We repeatedly measured resting metabolic rate, evaporative water loss (EWL) and heat tolerance in adult wild-derived captive zebra finches (n = 44) at increasing air temperatures up to 44 °C. We found high within-individual repeatability in thermoregulatory patterns, with heat-calling triggered at an individual-specific stage of panting. As expected for thermoregulatory mechanisms, both silent panting and heat-calling significantly increased EWL. However, only heat-calling resulted in greater heat tolerance, demonstrating that “vocal panting” brings a thermoregulatory benefit to the emitter. Our findings therefore not only improve our understanding of the evolution of passerine thermal adaptations, but also highlight a novel evolutionary precursor for acoustic signals. Nature Publishing Group UK 2020-11-03 /pmc/articles/PMC7609653/ /pubmed/33144650 http://dx.doi.org/10.1038/s41598-020-75909-6 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pessato, Anaïs
McKechnie, Andrew E.
Buchanan, Katherine L.
Mariette, Mylene M.
Vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird
title Vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird
title_full Vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird
title_fullStr Vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird
title_full_unstemmed Vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird
title_short Vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird
title_sort vocal panting: a novel thermoregulatory mechanism for enhancing heat tolerance in a desert-adapted bird
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609653/
https://www.ncbi.nlm.nih.gov/pubmed/33144650
http://dx.doi.org/10.1038/s41598-020-75909-6
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