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Developmental asynchrony might not reduce fitness in early life in painted turtles
Synchronous hatching and emergence of turtles from nests may be adaptive in predator avoidance during dispersal. However, little is known about the phenotypic consequences of such synchrony or the generality of predator avoidance in driving the evolution of this trait. Colbert et al. (2010) found th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459037/ https://www.ncbi.nlm.nih.gov/pubmed/36091403 http://dx.doi.org/10.3389/fphys.2022.923912 |
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author | Colbert, P. L. Spencer, R.-J. Janzen, F. J. |
author_facet | Colbert, P. L. Spencer, R.-J. Janzen, F. J. |
author_sort | Colbert, P. L. |
collection | PubMed |
description | Synchronous hatching and emergence of turtles from nests may be adaptive in predator avoidance during dispersal. However, little is known about the phenotypic consequences of such synchrony or the generality of predator avoidance in driving the evolution of this trait. Colbert et al. (2010) found that less advanced embryos hatched early in the presence of more advanced sibs, sustaining a persistent reduction in neuromuscular function. In this study, we experimentally assessed the influence of such accelerated embryonic development on hatching success, winter survival, and survival during terrestrial dispersal from the nest. Although we predicted that shortened incubation periods would reduce survival, early-hatching individuals suffered no detectable fitness costs at any stage considered in this study. Incubation temperature did not affect hatching success, and offspring sex did not affect survival across treatment groups. Incubation regime influenced offspring body size and was negatively correlated with dispersal time, however, there was no effect on survival during winter or terrestrial dispersal. Lack of a detectable fitness cost in these key early-life stages associated with hatching synchrony is consistent with a single, predator avoidance origin for this trait and retention in C. picta and other derived turtles via phylogenetic inertia. |
format | Online Article Text |
id | pubmed-9459037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94590372022-09-10 Developmental asynchrony might not reduce fitness in early life in painted turtles Colbert, P. L. Spencer, R.-J. Janzen, F. J. Front Physiol Physiology Synchronous hatching and emergence of turtles from nests may be adaptive in predator avoidance during dispersal. However, little is known about the phenotypic consequences of such synchrony or the generality of predator avoidance in driving the evolution of this trait. Colbert et al. (2010) found that less advanced embryos hatched early in the presence of more advanced sibs, sustaining a persistent reduction in neuromuscular function. In this study, we experimentally assessed the influence of such accelerated embryonic development on hatching success, winter survival, and survival during terrestrial dispersal from the nest. Although we predicted that shortened incubation periods would reduce survival, early-hatching individuals suffered no detectable fitness costs at any stage considered in this study. Incubation temperature did not affect hatching success, and offspring sex did not affect survival across treatment groups. Incubation regime influenced offspring body size and was negatively correlated with dispersal time, however, there was no effect on survival during winter or terrestrial dispersal. Lack of a detectable fitness cost in these key early-life stages associated with hatching synchrony is consistent with a single, predator avoidance origin for this trait and retention in C. picta and other derived turtles via phylogenetic inertia. Frontiers Media S.A. 2022-08-26 /pmc/articles/PMC9459037/ /pubmed/36091403 http://dx.doi.org/10.3389/fphys.2022.923912 Text en Copyright © 2022 Colbert, Spencer and Janzen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Colbert, P. L. Spencer, R.-J. Janzen, F. J. Developmental asynchrony might not reduce fitness in early life in painted turtles |
title | Developmental asynchrony might not reduce fitness in early life in painted turtles |
title_full | Developmental asynchrony might not reduce fitness in early life in painted turtles |
title_fullStr | Developmental asynchrony might not reduce fitness in early life in painted turtles |
title_full_unstemmed | Developmental asynchrony might not reduce fitness in early life in painted turtles |
title_short | Developmental asynchrony might not reduce fitness in early life in painted turtles |
title_sort | developmental asynchrony might not reduce fitness in early life in painted turtles |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459037/ https://www.ncbi.nlm.nih.gov/pubmed/36091403 http://dx.doi.org/10.3389/fphys.2022.923912 |
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