Cargando…
A highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of Anolis lizards
Diversifications often proceed along highly conserved, evolutionary trajectories. These patterns of covariation arise in ontogeny, which raises the possibility that adaptive morphologies are biased towards trait covariations that resemble growth trajectories. Here, we test this prediction in the div...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220270/ https://www.ncbi.nlm.nih.gov/pubmed/34157873 http://dx.doi.org/10.1098/rspb.2021.0226 |
_version_ | 1783711113012051968 |
---|---|
author | Feiner, Nathalie Jackson, Illiam S. C. Van der Cruyssen, Eliane Uller, Tobias |
author_facet | Feiner, Nathalie Jackson, Illiam S. C. Van der Cruyssen, Eliane Uller, Tobias |
author_sort | Feiner, Nathalie |
collection | PubMed |
description | Diversifications often proceed along highly conserved, evolutionary trajectories. These patterns of covariation arise in ontogeny, which raises the possibility that adaptive morphologies are biased towards trait covariations that resemble growth trajectories. Here, we test this prediction in the diverse clade of Anolis lizards by investigating the covariation of embryonic growth of 13 fore- and hindlimb bones in 15 species, and compare these to the evolutionary covariation of these limb bones across 267 Anolis species. Our results demonstrate that species differences in relative limb length are established already at hatching, and are resulting from both differential growth and differential sizes of cartilaginous anlagen. Multivariate analysis revealed that Antillean Anolis share a common ontogenetic allometry that is characterized by positive allometric growth of the long bones relative to metapodial and phalangeal bones. This major axis of ontogenetic allometry in limb bones deviated from the major axis of evolutionary allometry of the Antillean Anolis and the two clades of mainland Anolis lizards. These results demonstrate that the remarkable diversification of locomotor specialists in Anolis lizards are accessible through changes that are largely independent from ontogenetic growth trajectories, and therefore likely to be the result of modifications that manifest at the earliest stages of limb development. |
format | Online Article Text |
id | pubmed-8220270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82202702021-07-01 A highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of Anolis lizards Feiner, Nathalie Jackson, Illiam S. C. Van der Cruyssen, Eliane Uller, Tobias Proc Biol Sci Evolution Diversifications often proceed along highly conserved, evolutionary trajectories. These patterns of covariation arise in ontogeny, which raises the possibility that adaptive morphologies are biased towards trait covariations that resemble growth trajectories. Here, we test this prediction in the diverse clade of Anolis lizards by investigating the covariation of embryonic growth of 13 fore- and hindlimb bones in 15 species, and compare these to the evolutionary covariation of these limb bones across 267 Anolis species. Our results demonstrate that species differences in relative limb length are established already at hatching, and are resulting from both differential growth and differential sizes of cartilaginous anlagen. Multivariate analysis revealed that Antillean Anolis share a common ontogenetic allometry that is characterized by positive allometric growth of the long bones relative to metapodial and phalangeal bones. This major axis of ontogenetic allometry in limb bones deviated from the major axis of evolutionary allometry of the Antillean Anolis and the two clades of mainland Anolis lizards. These results demonstrate that the remarkable diversification of locomotor specialists in Anolis lizards are accessible through changes that are largely independent from ontogenetic growth trajectories, and therefore likely to be the result of modifications that manifest at the earliest stages of limb development. The Royal Society 2021-06-30 2021-06-23 /pmc/articles/PMC8220270/ /pubmed/34157873 http://dx.doi.org/10.1098/rspb.2021.0226 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolution Feiner, Nathalie Jackson, Illiam S. C. Van der Cruyssen, Eliane Uller, Tobias A highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of Anolis lizards |
title | A highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of Anolis lizards |
title_full | A highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of Anolis lizards |
title_fullStr | A highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of Anolis lizards |
title_full_unstemmed | A highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of Anolis lizards |
title_short | A highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of Anolis lizards |
title_sort | highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of anolis lizards |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220270/ https://www.ncbi.nlm.nih.gov/pubmed/34157873 http://dx.doi.org/10.1098/rspb.2021.0226 |
work_keys_str_mv | AT feinernathalie ahighlyconservedontogeneticlimballometryanditsevolutionarysignificanceintheadaptiveradiationofanolislizards AT jacksonilliamsc ahighlyconservedontogeneticlimballometryanditsevolutionarysignificanceintheadaptiveradiationofanolislizards AT vandercruysseneliane ahighlyconservedontogeneticlimballometryanditsevolutionarysignificanceintheadaptiveradiationofanolislizards AT ullertobias ahighlyconservedontogeneticlimballometryanditsevolutionarysignificanceintheadaptiveradiationofanolislizards AT feinernathalie highlyconservedontogeneticlimballometryanditsevolutionarysignificanceintheadaptiveradiationofanolislizards AT jacksonilliamsc highlyconservedontogeneticlimballometryanditsevolutionarysignificanceintheadaptiveradiationofanolislizards AT vandercruysseneliane highlyconservedontogeneticlimballometryanditsevolutionarysignificanceintheadaptiveradiationofanolislizards AT ullertobias highlyconservedontogeneticlimballometryanditsevolutionarysignificanceintheadaptiveradiationofanolislizards |