Cargando…

Maternal behavioral thermoregulation facilitated evolutionary transitions from egg laying to live birth

Live birth is a key innovation that has evolved from egg-laying ancestors over 100 times in reptiles. However, egg-laying lizards and snakes can have preferred body temperatures that are lethal to developing embryos, which should select against prolonged egg retention. Here, we demonstrate that ther...

Descripción completa

Detalles Bibliográficos
Autores principales: Pettersen, Amanda K, Feiner, Nathalie, Noble, Daniel W A, While, Geoffrey M, Uller, Tobias, Cornwallis, Charlie K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565886/
https://www.ncbi.nlm.nih.gov/pubmed/37829499
http://dx.doi.org/10.1093/evlett/qrad031
_version_ 1785118793146564608
author Pettersen, Amanda K
Feiner, Nathalie
Noble, Daniel W A
While, Geoffrey M
Uller, Tobias
Cornwallis, Charlie K
author_facet Pettersen, Amanda K
Feiner, Nathalie
Noble, Daniel W A
While, Geoffrey M
Uller, Tobias
Cornwallis, Charlie K
author_sort Pettersen, Amanda K
collection PubMed
description Live birth is a key innovation that has evolved from egg-laying ancestors over 100 times in reptiles. However, egg-laying lizards and snakes can have preferred body temperatures that are lethal to developing embryos, which should select against prolonged egg retention. Here, we demonstrate that thermal mismatches between mothers and offspring are widespread across the squamate phylogeny. This mismatch is resolved by gravid females adjusting their body temperature towards the thermal optimum of their embryos. We find that the same response occurs in both live-bearing and egg-laying species, despite the latter only retaining embryos during the early stages of development. Importantly, phylogenetic reconstructions suggest this thermoregulatory behavior in gravid females evolved in egg-laying species prior to the evolution of live birth. Maternal thermoregulatory behavior, therefore, bypasses the constraints imposed by a slowly evolving thermal physiology and has likely been a key facilitator in the repeated transition to live birth.
format Online
Article
Text
id pubmed-10565886
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-105658862023-10-12 Maternal behavioral thermoregulation facilitated evolutionary transitions from egg laying to live birth Pettersen, Amanda K Feiner, Nathalie Noble, Daniel W A While, Geoffrey M Uller, Tobias Cornwallis, Charlie K Evol Lett Letters Live birth is a key innovation that has evolved from egg-laying ancestors over 100 times in reptiles. However, egg-laying lizards and snakes can have preferred body temperatures that are lethal to developing embryos, which should select against prolonged egg retention. Here, we demonstrate that thermal mismatches between mothers and offspring are widespread across the squamate phylogeny. This mismatch is resolved by gravid females adjusting their body temperature towards the thermal optimum of their embryos. We find that the same response occurs in both live-bearing and egg-laying species, despite the latter only retaining embryos during the early stages of development. Importantly, phylogenetic reconstructions suggest this thermoregulatory behavior in gravid females evolved in egg-laying species prior to the evolution of live birth. Maternal thermoregulatory behavior, therefore, bypasses the constraints imposed by a slowly evolving thermal physiology and has likely been a key facilitator in the repeated transition to live birth. Oxford University Press 2023-07-26 /pmc/articles/PMC10565886/ /pubmed/37829499 http://dx.doi.org/10.1093/evlett/qrad031 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of The Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEN). https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Pettersen, Amanda K
Feiner, Nathalie
Noble, Daniel W A
While, Geoffrey M
Uller, Tobias
Cornwallis, Charlie K
Maternal behavioral thermoregulation facilitated evolutionary transitions from egg laying to live birth
title Maternal behavioral thermoregulation facilitated evolutionary transitions from egg laying to live birth
title_full Maternal behavioral thermoregulation facilitated evolutionary transitions from egg laying to live birth
title_fullStr Maternal behavioral thermoregulation facilitated evolutionary transitions from egg laying to live birth
title_full_unstemmed Maternal behavioral thermoregulation facilitated evolutionary transitions from egg laying to live birth
title_short Maternal behavioral thermoregulation facilitated evolutionary transitions from egg laying to live birth
title_sort maternal behavioral thermoregulation facilitated evolutionary transitions from egg laying to live birth
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565886/
https://www.ncbi.nlm.nih.gov/pubmed/37829499
http://dx.doi.org/10.1093/evlett/qrad031
work_keys_str_mv AT pettersenamandak maternalbehavioralthermoregulationfacilitatedevolutionarytransitionsfromegglayingtolivebirth
AT feinernathalie maternalbehavioralthermoregulationfacilitatedevolutionarytransitionsfromegglayingtolivebirth
AT nobledanielwa maternalbehavioralthermoregulationfacilitatedevolutionarytransitionsfromegglayingtolivebirth
AT whilegeoffreym maternalbehavioralthermoregulationfacilitatedevolutionarytransitionsfromegglayingtolivebirth
AT ullertobias maternalbehavioralthermoregulationfacilitatedevolutionarytransitionsfromegglayingtolivebirth
AT cornwallischarliek maternalbehavioralthermoregulationfacilitatedevolutionarytransitionsfromegglayingtolivebirth