Cargando…

Divergent vertebral formulae shape the evolution of axial complexity in mammals

Complexity, defined as the number of parts and their degree of differentiation, is a poorly explored aspect of macroevolutionary dynamics. The maximum anatomical complexity of organisms has undoubtedly increased through evolutionary time. However, it is unclear whether this increase is a purely diff...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Yimeng, Brinkworth, Andrew, Green, Emily, Oyston, Jack, Wills, Matthew, Ruta, Marcello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998275/
https://www.ncbi.nlm.nih.gov/pubmed/36878987
http://dx.doi.org/10.1038/s41559-023-01982-5
_version_ 1784903440604856320
author Li, Yimeng
Brinkworth, Andrew
Green, Emily
Oyston, Jack
Wills, Matthew
Ruta, Marcello
author_facet Li, Yimeng
Brinkworth, Andrew
Green, Emily
Oyston, Jack
Wills, Matthew
Ruta, Marcello
author_sort Li, Yimeng
collection PubMed
description Complexity, defined as the number of parts and their degree of differentiation, is a poorly explored aspect of macroevolutionary dynamics. The maximum anatomical complexity of organisms has undoubtedly increased through evolutionary time. However, it is unclear whether this increase is a purely diffusive process or whether it is at least partly driven, occurring in parallel in most or many lineages and with increases in the minima as well as the means. Highly differentiated and serially repeated structures, such as vertebrae, are useful systems with which to investigate these patterns. We focus on the serial differentiation of the vertebral column in 1,136 extant mammal species, using two indices that quantify complexity as the numerical richness and proportional distribution of vertebrae across presacral regions and a third expressing the ratio between thoracic and lumbar vertebrae. We address three questions. First, we ask whether the distribution of complexity values in major mammal groups is similar or whether clades have specific signatures associated with their ecology. Second, we ask whether changes in complexity throughout the phylogeny are biased towards increases and whether there is evidence of driven trends. Third, we ask whether evolutionary shifts in complexity depart from a uniform Brownian motion model. Vertebral counts, but not complexity indices, differ significantly between major groups and exhibit greater within-group variation than recognized hitherto. We find strong evidence of a trend towards increasing complexity, where higher values propagate further increases in descendant lineages. Several increases are inferred to have coincided with major ecological or environmental shifts. We find support for multiple-rate models of evolution for all complexity metrics, suggesting that increases in complexity occurred in stepwise shifts, with evidence for widespread episodes of recent rapid divergence. Different subclades evolve more complex vertebral columns in different configurations and probably under different selective pressures and constraints, with widespread convergence on the same formulae. Further work should therefore focus on the ecological relevance of differences in complexity and a more detailed understanding of historical patterns.
format Online
Article
Text
id pubmed-9998275
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-99982752023-03-11 Divergent vertebral formulae shape the evolution of axial complexity in mammals Li, Yimeng Brinkworth, Andrew Green, Emily Oyston, Jack Wills, Matthew Ruta, Marcello Nat Ecol Evol Article Complexity, defined as the number of parts and their degree of differentiation, is a poorly explored aspect of macroevolutionary dynamics. The maximum anatomical complexity of organisms has undoubtedly increased through evolutionary time. However, it is unclear whether this increase is a purely diffusive process or whether it is at least partly driven, occurring in parallel in most or many lineages and with increases in the minima as well as the means. Highly differentiated and serially repeated structures, such as vertebrae, are useful systems with which to investigate these patterns. We focus on the serial differentiation of the vertebral column in 1,136 extant mammal species, using two indices that quantify complexity as the numerical richness and proportional distribution of vertebrae across presacral regions and a third expressing the ratio between thoracic and lumbar vertebrae. We address three questions. First, we ask whether the distribution of complexity values in major mammal groups is similar or whether clades have specific signatures associated with their ecology. Second, we ask whether changes in complexity throughout the phylogeny are biased towards increases and whether there is evidence of driven trends. Third, we ask whether evolutionary shifts in complexity depart from a uniform Brownian motion model. Vertebral counts, but not complexity indices, differ significantly between major groups and exhibit greater within-group variation than recognized hitherto. We find strong evidence of a trend towards increasing complexity, where higher values propagate further increases in descendant lineages. Several increases are inferred to have coincided with major ecological or environmental shifts. We find support for multiple-rate models of evolution for all complexity metrics, suggesting that increases in complexity occurred in stepwise shifts, with evidence for widespread episodes of recent rapid divergence. Different subclades evolve more complex vertebral columns in different configurations and probably under different selective pressures and constraints, with widespread convergence on the same formulae. Further work should therefore focus on the ecological relevance of differences in complexity and a more detailed understanding of historical patterns. Nature Publishing Group UK 2023-03-06 2023 /pmc/articles/PMC9998275/ /pubmed/36878987 http://dx.doi.org/10.1038/s41559-023-01982-5 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
Li, Yimeng
Brinkworth, Andrew
Green, Emily
Oyston, Jack
Wills, Matthew
Ruta, Marcello
Divergent vertebral formulae shape the evolution of axial complexity in mammals
title Divergent vertebral formulae shape the evolution of axial complexity in mammals
title_full Divergent vertebral formulae shape the evolution of axial complexity in mammals
title_fullStr Divergent vertebral formulae shape the evolution of axial complexity in mammals
title_full_unstemmed Divergent vertebral formulae shape the evolution of axial complexity in mammals
title_short Divergent vertebral formulae shape the evolution of axial complexity in mammals
title_sort divergent vertebral formulae shape the evolution of axial complexity in mammals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998275/
https://www.ncbi.nlm.nih.gov/pubmed/36878987
http://dx.doi.org/10.1038/s41559-023-01982-5
work_keys_str_mv AT liyimeng divergentvertebralformulaeshapetheevolutionofaxialcomplexityinmammals
AT brinkworthandrew divergentvertebralformulaeshapetheevolutionofaxialcomplexityinmammals
AT greenemily divergentvertebralformulaeshapetheevolutionofaxialcomplexityinmammals
AT oystonjack divergentvertebralformulaeshapetheevolutionofaxialcomplexityinmammals
AT willsmatthew divergentvertebralformulaeshapetheevolutionofaxialcomplexityinmammals
AT rutamarcello divergentvertebralformulaeshapetheevolutionofaxialcomplexityinmammals