Cargando…

Temperature-Dependent Evolutionary Speed Shapes the Evolution of Biodiversity Patterns Across Tetrapod Radiations

Biodiversity varies predictably with environmental energy around the globe, but the underlaying mechanisms remain incompletely understood. The evolutionary speed hypothesis predicts that environmental kinetic energy shapes variation in speciation rates through temperature- or life history-dependent...

Descripción completa

Detalles Bibliográficos
Autores principales: Skeels, A, Bach, W, Hagen, O, Jetz, W, Pellissier, L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275562/
https://www.ncbi.nlm.nih.gov/pubmed/35809070
http://dx.doi.org/10.1093/sysbio/syac048
_version_ 1785059898477772800
author Skeels, A
Bach, W
Hagen, O
Jetz, W
Pellissier, L
author_facet Skeels, A
Bach, W
Hagen, O
Jetz, W
Pellissier, L
author_sort Skeels, A
collection PubMed
description Biodiversity varies predictably with environmental energy around the globe, but the underlaying mechanisms remain incompletely understood. The evolutionary speed hypothesis predicts that environmental kinetic energy shapes variation in speciation rates through temperature- or life history-dependent rates of evolution. To test whether variation in evolutionary speed can explain the relationship between energy and biodiversity in birds, mammals, amphibians, and reptiles, we simulated diversification over 65 myr of geological and climatic change with a spatially explicit eco-evolutionary simulation model. We modeled four distinct evolutionary scenarios in which speciation-completion rates were dependent on temperature (M1), life history (M2), temperature and life history (M3), or were independent of temperature and life-history (M0). To assess the agreement between simulated and empirical data, we performed model selection by fitting supervised machine learning models to multidimensional biodiversity patterns. We show that a model with temperature-dependent rates of speciation (M1) consistently had the strongest support. In contrast to statistical inferences, which showed no general relationships between temperature and speciation rates in tetrapods, we demonstrate how process-based modeling can disentangle the causes behind empirical biodiversity patterns. Our study highlights how environmental energy has played a fundamental role in the evolution of biodiversity over deep time. [Biogeography; diversification; machine learning; macroevolution; molecular evolution; simulation.]
format Online
Article
Text
id pubmed-10275562
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-102755622023-06-17 Temperature-Dependent Evolutionary Speed Shapes the Evolution of Biodiversity Patterns Across Tetrapod Radiations Skeels, A Bach, W Hagen, O Jetz, W Pellissier, L Syst Biol Regular Articles Biodiversity varies predictably with environmental energy around the globe, but the underlaying mechanisms remain incompletely understood. The evolutionary speed hypothesis predicts that environmental kinetic energy shapes variation in speciation rates through temperature- or life history-dependent rates of evolution. To test whether variation in evolutionary speed can explain the relationship between energy and biodiversity in birds, mammals, amphibians, and reptiles, we simulated diversification over 65 myr of geological and climatic change with a spatially explicit eco-evolutionary simulation model. We modeled four distinct evolutionary scenarios in which speciation-completion rates were dependent on temperature (M1), life history (M2), temperature and life history (M3), or were independent of temperature and life-history (M0). To assess the agreement between simulated and empirical data, we performed model selection by fitting supervised machine learning models to multidimensional biodiversity patterns. We show that a model with temperature-dependent rates of speciation (M1) consistently had the strongest support. In contrast to statistical inferences, which showed no general relationships between temperature and speciation rates in tetrapods, we demonstrate how process-based modeling can disentangle the causes behind empirical biodiversity patterns. Our study highlights how environmental energy has played a fundamental role in the evolution of biodiversity over deep time. [Biogeography; diversification; machine learning; macroevolution; molecular evolution; simulation.] Oxford University Press 2022-07-09 /pmc/articles/PMC10275562/ /pubmed/35809070 http://dx.doi.org/10.1093/sysbio/syac048 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society of Systematic Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Articles
Skeels, A
Bach, W
Hagen, O
Jetz, W
Pellissier, L
Temperature-Dependent Evolutionary Speed Shapes the Evolution of Biodiversity Patterns Across Tetrapod Radiations
title Temperature-Dependent Evolutionary Speed Shapes the Evolution of Biodiversity Patterns Across Tetrapod Radiations
title_full Temperature-Dependent Evolutionary Speed Shapes the Evolution of Biodiversity Patterns Across Tetrapod Radiations
title_fullStr Temperature-Dependent Evolutionary Speed Shapes the Evolution of Biodiversity Patterns Across Tetrapod Radiations
title_full_unstemmed Temperature-Dependent Evolutionary Speed Shapes the Evolution of Biodiversity Patterns Across Tetrapod Radiations
title_short Temperature-Dependent Evolutionary Speed Shapes the Evolution of Biodiversity Patterns Across Tetrapod Radiations
title_sort temperature-dependent evolutionary speed shapes the evolution of biodiversity patterns across tetrapod radiations
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275562/
https://www.ncbi.nlm.nih.gov/pubmed/35809070
http://dx.doi.org/10.1093/sysbio/syac048
work_keys_str_mv AT skeelsa temperaturedependentevolutionaryspeedshapestheevolutionofbiodiversitypatternsacrosstetrapodradiations
AT bachw temperaturedependentevolutionaryspeedshapestheevolutionofbiodiversitypatternsacrosstetrapodradiations
AT hageno temperaturedependentevolutionaryspeedshapestheevolutionofbiodiversitypatternsacrosstetrapodradiations
AT jetzw temperaturedependentevolutionaryspeedshapestheevolutionofbiodiversitypatternsacrosstetrapodradiations
AT pellissierl temperaturedependentevolutionaryspeedshapestheevolutionofbiodiversitypatternsacrosstetrapodradiations