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Linking scaling laws across eukaryotes

Scaling laws relating body mass to species characteristics are among the most universal quantitative patterns in biology. Within major taxonomic groups, the 4 key ecological variables of metabolism, abundance, growth, and mortality are often well described by power laws with exponents near 3/4 or re...

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Autores principales: Hatton, Ian A., Dobson, Andy P., Storch, David, Galbraith, Eric D., Loreau, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815163/
https://www.ncbi.nlm.nih.gov/pubmed/31591216
http://dx.doi.org/10.1073/pnas.1900492116
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author Hatton, Ian A.
Dobson, Andy P.
Storch, David
Galbraith, Eric D.
Loreau, Michel
author_facet Hatton, Ian A.
Dobson, Andy P.
Storch, David
Galbraith, Eric D.
Loreau, Michel
author_sort Hatton, Ian A.
collection PubMed
description Scaling laws relating body mass to species characteristics are among the most universal quantitative patterns in biology. Within major taxonomic groups, the 4 key ecological variables of metabolism, abundance, growth, and mortality are often well described by power laws with exponents near 3/4 or related to that value, a commonality often attributed to biophysical constraints on metabolism. However, metabolic scaling theories remain widely debated, and the links among the 4 variables have never been formally tested across the full domain of eukaryote life, to which prevailing theory applies. Here we present datasets of unprecedented scope to examine these 4 scaling laws across all eukaryotes and link them to test whether their combinations support theoretical expectations. We find that metabolism and abundance scale with body size in a remarkably reciprocal fashion, with exponents near ±3/4 within groups, as expected from metabolic theory, but with exponents near ±1 across all groups. This reciprocal scaling supports “energetic equivalence” across eukaryotes, which hypothesizes that the partitioning of energy in space across species does not vary significantly with body size. In contrast, growth and mortality rates scale similarly both within and across groups, with exponents of ±1/4. These findings are inconsistent with a metabolic basis for growth and mortality scaling across eukaryotes. We propose that rather than limiting growth, metabolism adjusts to the needs of growth within major groups, and that growth dynamics may offer a viable theoretical basis to biological scaling.
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spelling pubmed-68151632019-10-30 Linking scaling laws across eukaryotes Hatton, Ian A. Dobson, Andy P. Storch, David Galbraith, Eric D. Loreau, Michel Proc Natl Acad Sci U S A Biological Sciences Scaling laws relating body mass to species characteristics are among the most universal quantitative patterns in biology. Within major taxonomic groups, the 4 key ecological variables of metabolism, abundance, growth, and mortality are often well described by power laws with exponents near 3/4 or related to that value, a commonality often attributed to biophysical constraints on metabolism. However, metabolic scaling theories remain widely debated, and the links among the 4 variables have never been formally tested across the full domain of eukaryote life, to which prevailing theory applies. Here we present datasets of unprecedented scope to examine these 4 scaling laws across all eukaryotes and link them to test whether their combinations support theoretical expectations. We find that metabolism and abundance scale with body size in a remarkably reciprocal fashion, with exponents near ±3/4 within groups, as expected from metabolic theory, but with exponents near ±1 across all groups. This reciprocal scaling supports “energetic equivalence” across eukaryotes, which hypothesizes that the partitioning of energy in space across species does not vary significantly with body size. In contrast, growth and mortality rates scale similarly both within and across groups, with exponents of ±1/4. These findings are inconsistent with a metabolic basis for growth and mortality scaling across eukaryotes. We propose that rather than limiting growth, metabolism adjusts to the needs of growth within major groups, and that growth dynamics may offer a viable theoretical basis to biological scaling. National Academy of Sciences 2019-10-22 2019-10-07 /pmc/articles/PMC6815163/ /pubmed/31591216 http://dx.doi.org/10.1073/pnas.1900492116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Hatton, Ian A.
Dobson, Andy P.
Storch, David
Galbraith, Eric D.
Loreau, Michel
Linking scaling laws across eukaryotes
title Linking scaling laws across eukaryotes
title_full Linking scaling laws across eukaryotes
title_fullStr Linking scaling laws across eukaryotes
title_full_unstemmed Linking scaling laws across eukaryotes
title_short Linking scaling laws across eukaryotes
title_sort linking scaling laws across eukaryotes
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815163/
https://www.ncbi.nlm.nih.gov/pubmed/31591216
http://dx.doi.org/10.1073/pnas.1900492116
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