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Functional reorganisation of the cranial skeleton during the cynodont–mammaliaform transition

Skeletal simplification occurred in multiple vertebrate clades over the last 500 million years, including the evolution from premammalian cynodonts to mammals. This transition is characterised by the loss and reduction of cranial bones, the emergence of a novel jaw joint, and the rearrangement of th...

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Autores principales: Lautenschlager, Stephan, Fagan, Michael J., Luo, Zhe-Xi, Bird, Charlotte M., Gill, Pamela, Rayfield, Emily J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10097706/
https://www.ncbi.nlm.nih.gov/pubmed/37046052
http://dx.doi.org/10.1038/s42003-023-04742-0
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author Lautenschlager, Stephan
Fagan, Michael J.
Luo, Zhe-Xi
Bird, Charlotte M.
Gill, Pamela
Rayfield, Emily J.
author_facet Lautenschlager, Stephan
Fagan, Michael J.
Luo, Zhe-Xi
Bird, Charlotte M.
Gill, Pamela
Rayfield, Emily J.
author_sort Lautenschlager, Stephan
collection PubMed
description Skeletal simplification occurred in multiple vertebrate clades over the last 500 million years, including the evolution from premammalian cynodonts to mammals. This transition is characterised by the loss and reduction of cranial bones, the emergence of a novel jaw joint, and the rearrangement of the jaw musculature. These modifications have long been hypothesised to increase skull strength and efficiency during feeding. Here, we combine digital reconstruction and biomechanical modelling to show that there is no evidence for an increase in cranial strength and biomechanical performance. Our analyses demonstrate the selective functional reorganisation of the cranial skeleton, leading to reduced stresses in the braincase and the skull roof but increased stresses in the zygomatic region through this transition. This cranial functional reorganisation, reduction in mechanical advantage, and overall miniaturisation in body size are linked with a dietary specialisation to insectivory, permitting the subsequent morphological and ecological diversification of the mammalian lineage.
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spelling pubmed-100977062023-04-14 Functional reorganisation of the cranial skeleton during the cynodont–mammaliaform transition Lautenschlager, Stephan Fagan, Michael J. Luo, Zhe-Xi Bird, Charlotte M. Gill, Pamela Rayfield, Emily J. Commun Biol Article Skeletal simplification occurred in multiple vertebrate clades over the last 500 million years, including the evolution from premammalian cynodonts to mammals. This transition is characterised by the loss and reduction of cranial bones, the emergence of a novel jaw joint, and the rearrangement of the jaw musculature. These modifications have long been hypothesised to increase skull strength and efficiency during feeding. Here, we combine digital reconstruction and biomechanical modelling to show that there is no evidence for an increase in cranial strength and biomechanical performance. Our analyses demonstrate the selective functional reorganisation of the cranial skeleton, leading to reduced stresses in the braincase and the skull roof but increased stresses in the zygomatic region through this transition. This cranial functional reorganisation, reduction in mechanical advantage, and overall miniaturisation in body size are linked with a dietary specialisation to insectivory, permitting the subsequent morphological and ecological diversification of the mammalian lineage. Nature Publishing Group UK 2023-04-12 /pmc/articles/PMC10097706/ /pubmed/37046052 http://dx.doi.org/10.1038/s42003-023-04742-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lautenschlager, Stephan
Fagan, Michael J.
Luo, Zhe-Xi
Bird, Charlotte M.
Gill, Pamela
Rayfield, Emily J.
Functional reorganisation of the cranial skeleton during the cynodont–mammaliaform transition
title Functional reorganisation of the cranial skeleton during the cynodont–mammaliaform transition
title_full Functional reorganisation of the cranial skeleton during the cynodont–mammaliaform transition
title_fullStr Functional reorganisation of the cranial skeleton during the cynodont–mammaliaform transition
title_full_unstemmed Functional reorganisation of the cranial skeleton during the cynodont–mammaliaform transition
title_short Functional reorganisation of the cranial skeleton during the cynodont–mammaliaform transition
title_sort functional reorganisation of the cranial skeleton during the cynodont–mammaliaform transition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10097706/
https://www.ncbi.nlm.nih.gov/pubmed/37046052
http://dx.doi.org/10.1038/s42003-023-04742-0
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