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Body mass predicts isotope enrichment in herbivorous mammals

Carbon isotopic signatures recorded in vertebrate tissues derive from ingested food and thus reflect ecologies and ecosystems. For almost two decades, most carbon isotope-based ecological interpretations of extant and extinct herbivorous mammals have used a single diet–bioapatite enrichment value (1...

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Autores principales: Tejada-Lara, Julia V., MacFadden, Bruce J., Bermudez, Lizette, Rojas, Gianmarco, Salas-Gismondi, Rodolfo, Flynn, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030519/
https://www.ncbi.nlm.nih.gov/pubmed/30051854
http://dx.doi.org/10.1098/rspb.2018.1020
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author Tejada-Lara, Julia V.
MacFadden, Bruce J.
Bermudez, Lizette
Rojas, Gianmarco
Salas-Gismondi, Rodolfo
Flynn, John J.
author_facet Tejada-Lara, Julia V.
MacFadden, Bruce J.
Bermudez, Lizette
Rojas, Gianmarco
Salas-Gismondi, Rodolfo
Flynn, John J.
author_sort Tejada-Lara, Julia V.
collection PubMed
description Carbon isotopic signatures recorded in vertebrate tissues derive from ingested food and thus reflect ecologies and ecosystems. For almost two decades, most carbon isotope-based ecological interpretations of extant and extinct herbivorous mammals have used a single diet–bioapatite enrichment value (14‰). Assuming this single value applies to all herbivorous mammals, from tiny monkeys to giant elephants, it overlooks potential effects of distinct physiological and metabolic processes on carbon fractionation. By analysing a never before assessed herbivorous group spanning a broad range of body masses—sloths—we discovered considerable variation in diet–bioapatite δ(13)C enrichment among mammals. Statistical tests (ordinary least squares, quantile, robust regressions, Akaike information criterion model tests) document independence from phylogeny, and a previously unrecognized strong and significant correlation of δ(13)C enrichment with body mass for all mammalian herbivores. A single-factor body mass model outperforms all other single-factor or more complex combinatorial models evaluated, including for physiological variables (metabolic rate and body temperature proxies), and indicates that body mass alone predicts δ(13)C enrichment. These analyses, spanning more than 5 orders of magnitude of body sizes, yield a size-dependent prediction of isotopic enrichment across Mammalia and for distinct digestive physiologies, permitting reconstruction of foregut versus hindgut fermentation for fossils and refined mean annual palaeoprecipitation estimates based on δ(13)C of mammalian bioapatite.
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spelling pubmed-60305192018-07-22 Body mass predicts isotope enrichment in herbivorous mammals Tejada-Lara, Julia V. MacFadden, Bruce J. Bermudez, Lizette Rojas, Gianmarco Salas-Gismondi, Rodolfo Flynn, John J. Proc Biol Sci Evolution Carbon isotopic signatures recorded in vertebrate tissues derive from ingested food and thus reflect ecologies and ecosystems. For almost two decades, most carbon isotope-based ecological interpretations of extant and extinct herbivorous mammals have used a single diet–bioapatite enrichment value (14‰). Assuming this single value applies to all herbivorous mammals, from tiny monkeys to giant elephants, it overlooks potential effects of distinct physiological and metabolic processes on carbon fractionation. By analysing a never before assessed herbivorous group spanning a broad range of body masses—sloths—we discovered considerable variation in diet–bioapatite δ(13)C enrichment among mammals. Statistical tests (ordinary least squares, quantile, robust regressions, Akaike information criterion model tests) document independence from phylogeny, and a previously unrecognized strong and significant correlation of δ(13)C enrichment with body mass for all mammalian herbivores. A single-factor body mass model outperforms all other single-factor or more complex combinatorial models evaluated, including for physiological variables (metabolic rate and body temperature proxies), and indicates that body mass alone predicts δ(13)C enrichment. These analyses, spanning more than 5 orders of magnitude of body sizes, yield a size-dependent prediction of isotopic enrichment across Mammalia and for distinct digestive physiologies, permitting reconstruction of foregut versus hindgut fermentation for fossils and refined mean annual palaeoprecipitation estimates based on δ(13)C of mammalian bioapatite. The Royal Society 2018-06-27 2018-06-27 /pmc/articles/PMC6030519/ /pubmed/30051854 http://dx.doi.org/10.1098/rspb.2018.1020 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Tejada-Lara, Julia V.
MacFadden, Bruce J.
Bermudez, Lizette
Rojas, Gianmarco
Salas-Gismondi, Rodolfo
Flynn, John J.
Body mass predicts isotope enrichment in herbivorous mammals
title Body mass predicts isotope enrichment in herbivorous mammals
title_full Body mass predicts isotope enrichment in herbivorous mammals
title_fullStr Body mass predicts isotope enrichment in herbivorous mammals
title_full_unstemmed Body mass predicts isotope enrichment in herbivorous mammals
title_short Body mass predicts isotope enrichment in herbivorous mammals
title_sort body mass predicts isotope enrichment in herbivorous mammals
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030519/
https://www.ncbi.nlm.nih.gov/pubmed/30051854
http://dx.doi.org/10.1098/rspb.2018.1020
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