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Thermal physiology and activity in relation to reproductive status and sex in a free-ranging semelparous marsupial

In a changing climate, southern hemisphere mammals are predicted to face rising temperatures and aridity, resulting in food and water shortages, which may further challenge already constrained energetic demands. Especially semelparous mammals may be threatened because survival of the entire populati...

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Autores principales: Parker, Cassandra A, Geiser, Fritz, Stawski, Clare
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6846706/
https://www.ncbi.nlm.nih.gov/pubmed/31737272
http://dx.doi.org/10.1093/conphys/coz073
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author Parker, Cassandra A
Geiser, Fritz
Stawski, Clare
author_facet Parker, Cassandra A
Geiser, Fritz
Stawski, Clare
author_sort Parker, Cassandra A
collection PubMed
description In a changing climate, southern hemisphere mammals are predicted to face rising temperatures and aridity, resulting in food and water shortages, which may further challenge already constrained energetic demands. Especially semelparous mammals may be threatened because survival of the entire population depends on the success of a single breeding event. One of these species, the yellow-footed antechinus, Antechinus flavipes, a small, heterothermic marsupial mammal, commences reproduction during winter, when insect prey is limited and energetic constraints are high. We examined the inter-relations between thermal and foraging biology of free-ranging A. flavipes and examined whether they use torpor for energy conservation, despite the fact that reproduction and torpor are considered to be incompatible for many mammals. Females used torpor during the reproductive season, but patterns changed with reproductive status. Prior to breeding, females used frequent (86% of days), deep and long torpor that was more pronounced than any other reproductive group, including pre-mating males (64% of days). Pregnant females continued to use torpor, albeit torpor was less frequent (28% of days) and significantly shorter and shallower than before breeding. Parturient and lactating females did not express torpor. During the mating period, males reduced torpor use (24% of days). Pre-reproductive females and pre-mating males were the least active and may use torpor to minimize predator exposure and enhance fat deposition in anticipation of the energetic demands associated with impending mating, gestation and lactation. Reproductive females were most active and likely foraged and fed to promote growth and development of young. Our data show that A. flavipes are balancing energetic demands during the reproductive season by modifying torpor and activity patterns. As the timing of reproduction is fixed for this genus, it is probable that climate change will render these behavioural and physiological adaptations as inadequate and threaten this and other semelparous species.
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spelling pubmed-68467062019-11-15 Thermal physiology and activity in relation to reproductive status and sex in a free-ranging semelparous marsupial Parker, Cassandra A Geiser, Fritz Stawski, Clare Conserv Physiol Research Article In a changing climate, southern hemisphere mammals are predicted to face rising temperatures and aridity, resulting in food and water shortages, which may further challenge already constrained energetic demands. Especially semelparous mammals may be threatened because survival of the entire population depends on the success of a single breeding event. One of these species, the yellow-footed antechinus, Antechinus flavipes, a small, heterothermic marsupial mammal, commences reproduction during winter, when insect prey is limited and energetic constraints are high. We examined the inter-relations between thermal and foraging biology of free-ranging A. flavipes and examined whether they use torpor for energy conservation, despite the fact that reproduction and torpor are considered to be incompatible for many mammals. Females used torpor during the reproductive season, but patterns changed with reproductive status. Prior to breeding, females used frequent (86% of days), deep and long torpor that was more pronounced than any other reproductive group, including pre-mating males (64% of days). Pregnant females continued to use torpor, albeit torpor was less frequent (28% of days) and significantly shorter and shallower than before breeding. Parturient and lactating females did not express torpor. During the mating period, males reduced torpor use (24% of days). Pre-reproductive females and pre-mating males were the least active and may use torpor to minimize predator exposure and enhance fat deposition in anticipation of the energetic demands associated with impending mating, gestation and lactation. Reproductive females were most active and likely foraged and fed to promote growth and development of young. Our data show that A. flavipes are balancing energetic demands during the reproductive season by modifying torpor and activity patterns. As the timing of reproduction is fixed for this genus, it is probable that climate change will render these behavioural and physiological adaptations as inadequate and threaten this and other semelparous species. Oxford University Press 2019-11-11 /pmc/articles/PMC6846706/ /pubmed/31737272 http://dx.doi.org/10.1093/conphys/coz073 Text en © The Author(s) 2019. Published by Oxford University Press and the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Parker, Cassandra A
Geiser, Fritz
Stawski, Clare
Thermal physiology and activity in relation to reproductive status and sex in a free-ranging semelparous marsupial
title Thermal physiology and activity in relation to reproductive status and sex in a free-ranging semelparous marsupial
title_full Thermal physiology and activity in relation to reproductive status and sex in a free-ranging semelparous marsupial
title_fullStr Thermal physiology and activity in relation to reproductive status and sex in a free-ranging semelparous marsupial
title_full_unstemmed Thermal physiology and activity in relation to reproductive status and sex in a free-ranging semelparous marsupial
title_short Thermal physiology and activity in relation to reproductive status and sex in a free-ranging semelparous marsupial
title_sort thermal physiology and activity in relation to reproductive status and sex in a free-ranging semelparous marsupial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6846706/
https://www.ncbi.nlm.nih.gov/pubmed/31737272
http://dx.doi.org/10.1093/conphys/coz073
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