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Fossil bone histology reveals ancient origins for rapid juvenile growth in tetrapods
Patterns of growth throughout the lifetime of an animal reflect critical life history traits such as reproductive timing, physiology, and ecological interactions. The ancestral growth pattern for tetrapods has traditionally been described as slow-to-moderately paced, akin to modern amphibians, with...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705711/ https://www.ncbi.nlm.nih.gov/pubmed/36443424 http://dx.doi.org/10.1038/s42003-022-04079-0 |
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author | Whitney, Megan R. Otoo, Benjamin K. A. Angielczyk, Kenneth D. Pierce, Stephanie E. |
author_facet | Whitney, Megan R. Otoo, Benjamin K. A. Angielczyk, Kenneth D. Pierce, Stephanie E. |
author_sort | Whitney, Megan R. |
collection | PubMed |
description | Patterns of growth throughout the lifetime of an animal reflect critical life history traits such as reproductive timing, physiology, and ecological interactions. The ancestral growth pattern for tetrapods has traditionally been described as slow-to-moderately paced, akin to modern amphibians, with fast growth and high metabolic rates considered a specialized physiological trait of amniotes. Here, we present bone histology from an ontogenetic series of the Early Carboniferous stem tetrapod Whatcheeria deltae, and document evidence of fibrolamellar bone—primary bone tissue associated with fast growth. Our data indicate that Whatcheeria juveniles grew rapidly and reached skeletal maturity quickly, allowing them to occupy a large-bodied predator niche in their paleoenvironment. This life history strategy contrasts with those described for other stem tetrapods and indicates that a diversity of growth patterns existed at the origins of tetrapod diversification. Importantly, Whatcheeria marks an unexpectedly early occurrence of fibrolamellar bone in Tetrapoda, both temporally and phylogenetically. These findings reveal that elevated juvenile growth is not limited to amniotes, but has a deep history in the tetrapod clade and may have played a previously unrecognized role in the tetrapod invasion of land. |
format | Online Article Text |
id | pubmed-9705711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97057112022-11-30 Fossil bone histology reveals ancient origins for rapid juvenile growth in tetrapods Whitney, Megan R. Otoo, Benjamin K. A. Angielczyk, Kenneth D. Pierce, Stephanie E. Commun Biol Article Patterns of growth throughout the lifetime of an animal reflect critical life history traits such as reproductive timing, physiology, and ecological interactions. The ancestral growth pattern for tetrapods has traditionally been described as slow-to-moderately paced, akin to modern amphibians, with fast growth and high metabolic rates considered a specialized physiological trait of amniotes. Here, we present bone histology from an ontogenetic series of the Early Carboniferous stem tetrapod Whatcheeria deltae, and document evidence of fibrolamellar bone—primary bone tissue associated with fast growth. Our data indicate that Whatcheeria juveniles grew rapidly and reached skeletal maturity quickly, allowing them to occupy a large-bodied predator niche in their paleoenvironment. This life history strategy contrasts with those described for other stem tetrapods and indicates that a diversity of growth patterns existed at the origins of tetrapod diversification. Importantly, Whatcheeria marks an unexpectedly early occurrence of fibrolamellar bone in Tetrapoda, both temporally and phylogenetically. These findings reveal that elevated juvenile growth is not limited to amniotes, but has a deep history in the tetrapod clade and may have played a previously unrecognized role in the tetrapod invasion of land. Nature Publishing Group UK 2022-11-28 /pmc/articles/PMC9705711/ /pubmed/36443424 http://dx.doi.org/10.1038/s42003-022-04079-0 Text en © The Author(s) 2022 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 Whitney, Megan R. Otoo, Benjamin K. A. Angielczyk, Kenneth D. Pierce, Stephanie E. Fossil bone histology reveals ancient origins for rapid juvenile growth in tetrapods |
title | Fossil bone histology reveals ancient origins for rapid juvenile growth in tetrapods |
title_full | Fossil bone histology reveals ancient origins for rapid juvenile growth in tetrapods |
title_fullStr | Fossil bone histology reveals ancient origins for rapid juvenile growth in tetrapods |
title_full_unstemmed | Fossil bone histology reveals ancient origins for rapid juvenile growth in tetrapods |
title_short | Fossil bone histology reveals ancient origins for rapid juvenile growth in tetrapods |
title_sort | fossil bone histology reveals ancient origins for rapid juvenile growth in tetrapods |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705711/ https://www.ncbi.nlm.nih.gov/pubmed/36443424 http://dx.doi.org/10.1038/s42003-022-04079-0 |
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