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A switch in jaw form–function coupling during the evolution of mammals
The evolutionary shift from a single-element ear, multi-element jaw to a multi-element ear, single-element jaw during the transition to crown mammals marks one of the most dramatic structural transformations in vertebrates. Research on this transformation has focused on mammalian middle-ear evolutio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184249/ https://www.ncbi.nlm.nih.gov/pubmed/37183899 http://dx.doi.org/10.1098/rstb.2022.0091 |
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author | Tseng, Z. Jack Garcia-Lara, Sergio Flynn, John J. Holmes, Emily Rowe, Timothy B. Dickson, Blake V. |
author_facet | Tseng, Z. Jack Garcia-Lara, Sergio Flynn, John J. Holmes, Emily Rowe, Timothy B. Dickson, Blake V. |
author_sort | Tseng, Z. Jack |
collection | PubMed |
description | The evolutionary shift from a single-element ear, multi-element jaw to a multi-element ear, single-element jaw during the transition to crown mammals marks one of the most dramatic structural transformations in vertebrates. Research on this transformation has focused on mammalian middle-ear evolution, but a mandible comprising only the dentary is equally emblematic of this evolutionary radiation. Here, we show that the remarkably diverse jaw shapes of crown mammals are coupled with surprisingly stereotyped jaw stiffness. This strength-based morphofunctional regime has a genetic basis and allowed mammalian jaws to effectively resist deformation as they radiated into highly disparate forms with markedly distinct diets. The main functional consequences for the mandible of decoupling hearing and mastication were a trade-off between higher jaw stiffness versus decreased mechanical efficiency and speed compared with non-mammals. This fundamental and consequential shift in jaw form–function underpins the ecological and taxonomic diversification of crown mammals. This article is part of the theme issue ‘The mammalian skull: development, structure and function’. |
format | Online Article Text |
id | pubmed-10184249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-101842492023-05-16 A switch in jaw form–function coupling during the evolution of mammals Tseng, Z. Jack Garcia-Lara, Sergio Flynn, John J. Holmes, Emily Rowe, Timothy B. Dickson, Blake V. Philos Trans R Soc Lond B Biol Sci Articles The evolutionary shift from a single-element ear, multi-element jaw to a multi-element ear, single-element jaw during the transition to crown mammals marks one of the most dramatic structural transformations in vertebrates. Research on this transformation has focused on mammalian middle-ear evolution, but a mandible comprising only the dentary is equally emblematic of this evolutionary radiation. Here, we show that the remarkably diverse jaw shapes of crown mammals are coupled with surprisingly stereotyped jaw stiffness. This strength-based morphofunctional regime has a genetic basis and allowed mammalian jaws to effectively resist deformation as they radiated into highly disparate forms with markedly distinct diets. The main functional consequences for the mandible of decoupling hearing and mastication were a trade-off between higher jaw stiffness versus decreased mechanical efficiency and speed compared with non-mammals. This fundamental and consequential shift in jaw form–function underpins the ecological and taxonomic diversification of crown mammals. This article is part of the theme issue ‘The mammalian skull: development, structure and function’. The Royal Society 2023-07-03 2023-05-15 /pmc/articles/PMC10184249/ /pubmed/37183899 http://dx.doi.org/10.1098/rstb.2022.0091 Text en © 2023 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 | Articles Tseng, Z. Jack Garcia-Lara, Sergio Flynn, John J. Holmes, Emily Rowe, Timothy B. Dickson, Blake V. A switch in jaw form–function coupling during the evolution of mammals |
title | A switch in jaw form–function coupling during the evolution of mammals |
title_full | A switch in jaw form–function coupling during the evolution of mammals |
title_fullStr | A switch in jaw form–function coupling during the evolution of mammals |
title_full_unstemmed | A switch in jaw form–function coupling during the evolution of mammals |
title_short | A switch in jaw form–function coupling during the evolution of mammals |
title_sort | switch in jaw form–function coupling during the evolution of mammals |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184249/ https://www.ncbi.nlm.nih.gov/pubmed/37183899 http://dx.doi.org/10.1098/rstb.2022.0091 |
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