Cargando…

Changing allometric relationships among fossil and Recent populations in two colonial species

Allometry is vital for understanding the mechanisms underlying phenotypic evolution. Despite a large body of literature on allometry, studies based on fossil time series are limited for solitary organisms and nonexistent for colonial organisms. Allometric relationships have been found to be relative...

Descripción completa

Detalles Bibliográficos
Autores principales: Di Martino, Emanuela, Liow, Lee Hsiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805184/
https://www.ncbi.nlm.nih.gov/pubmed/35993139
http://dx.doi.org/10.1111/evo.14598
_version_ 1784862285666189312
author Di Martino, Emanuela
Liow, Lee Hsiang
author_facet Di Martino, Emanuela
Liow, Lee Hsiang
author_sort Di Martino, Emanuela
collection PubMed
description Allometry is vital for understanding the mechanisms underlying phenotypic evolution. Despite a large body of literature on allometry, studies based on fossil time series are limited for solitary organisms and nonexistent for colonial organisms. Allometric relationships have been found to be relatively constant across Recent populations of the same species, separated by space, but variable among fossil populations separated by thousands of years. How stable are allometric relationships at the module level for colonial organisms? We address this question using two extant species of the cheilostome bryozoan Microporella with fossil records spanning the Pleistocene of New Zealand. We investigate size covariation between feeding modules and three traits with separate functions (reproductive, resource uptake, and defense). We found that within‐population (static) allometry can change on timescales of at least 0.1 million years. These within‐population relationships do not consistently predict overintraspecific evolutionary allometry, which in turn does not predict those estimated at the genus level. Different functional traits are constrained to different extents by module size with defensive traits being the least constrained and most evolvable, compared with reproductive and resource uptake traits. Our study highlights the potential of colonial organisms in understanding the constraints and drivers of long‐term phenotypic change.
format Online
Article
Text
id pubmed-9805184
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-98051842023-01-06 Changing allometric relationships among fossil and Recent populations in two colonial species Di Martino, Emanuela Liow, Lee Hsiang Evolution Original Articles Allometry is vital for understanding the mechanisms underlying phenotypic evolution. Despite a large body of literature on allometry, studies based on fossil time series are limited for solitary organisms and nonexistent for colonial organisms. Allometric relationships have been found to be relatively constant across Recent populations of the same species, separated by space, but variable among fossil populations separated by thousands of years. How stable are allometric relationships at the module level for colonial organisms? We address this question using two extant species of the cheilostome bryozoan Microporella with fossil records spanning the Pleistocene of New Zealand. We investigate size covariation between feeding modules and three traits with separate functions (reproductive, resource uptake, and defense). We found that within‐population (static) allometry can change on timescales of at least 0.1 million years. These within‐population relationships do not consistently predict overintraspecific evolutionary allometry, which in turn does not predict those estimated at the genus level. Different functional traits are constrained to different extents by module size with defensive traits being the least constrained and most evolvable, compared with reproductive and resource uptake traits. Our study highlights the potential of colonial organisms in understanding the constraints and drivers of long‐term phenotypic change. John Wiley and Sons Inc. 2022-08-29 2022-10 /pmc/articles/PMC9805184/ /pubmed/35993139 http://dx.doi.org/10.1111/evo.14598 Text en © 2022 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Di Martino, Emanuela
Liow, Lee Hsiang
Changing allometric relationships among fossil and Recent populations in two colonial species
title Changing allometric relationships among fossil and Recent populations in two colonial species
title_full Changing allometric relationships among fossil and Recent populations in two colonial species
title_fullStr Changing allometric relationships among fossil and Recent populations in two colonial species
title_full_unstemmed Changing allometric relationships among fossil and Recent populations in two colonial species
title_short Changing allometric relationships among fossil and Recent populations in two colonial species
title_sort changing allometric relationships among fossil and recent populations in two colonial species
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805184/
https://www.ncbi.nlm.nih.gov/pubmed/35993139
http://dx.doi.org/10.1111/evo.14598
work_keys_str_mv AT dimartinoemanuela changingallometricrelationshipsamongfossilandrecentpopulationsintwocolonialspecies
AT liowleehsiang changingallometricrelationshipsamongfossilandrecentpopulationsintwocolonialspecies