Cargando…

Solving the woolly mammoth conundrum: amino acid (15)N-enrichment suggests a distinct forage or habitat

Understanding woolly mammoth ecology is key to understanding Pleistocene community dynamics and evaluating the roles of human hunting and climate change in late Quaternary megafaunal extinctions. Previous isotopic studies of mammoths’ diet and physiology have been hampered by the ‘mammoth conundrum’...

Descripción completa

Detalles Bibliográficos
Autores principales: Schwartz-Narbonne, Rachel, Longstaffe, Fred J., Metcalfe, Jessica Z., Zazula, Grant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460640/
https://www.ncbi.nlm.nih.gov/pubmed/26056037
http://dx.doi.org/10.1038/srep09791
_version_ 1782375404096454656
author Schwartz-Narbonne, Rachel
Longstaffe, Fred J.
Metcalfe, Jessica Z.
Zazula, Grant
author_facet Schwartz-Narbonne, Rachel
Longstaffe, Fred J.
Metcalfe, Jessica Z.
Zazula, Grant
author_sort Schwartz-Narbonne, Rachel
collection PubMed
description Understanding woolly mammoth ecology is key to understanding Pleistocene community dynamics and evaluating the roles of human hunting and climate change in late Quaternary megafaunal extinctions. Previous isotopic studies of mammoths’ diet and physiology have been hampered by the ‘mammoth conundrum’: woolly mammoths have anomalously high collagen δ(15)N values, which are more similar to coeval carnivores than herbivores, and which could imply a distinct diet and (or) habitat, or a physiological adaptation. We analyzed individual amino acids from collagen of adult woolly mammoths and coeval species, and discovered greater  (15)N enrichment in source amino acids of woolly mammoths than in most other herbivores or carnivores. Woolly mammoths consumed an isotopically distinct food source, reflective of extreme aridity, dung fertilization, and (or) plant selection. This dietary signal suggests that woolly mammoths occupied a distinct habitat or forage niche relative to other Pleistocene herbivores.
format Online
Article
Text
id pubmed-4460640
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-44606402015-06-18 Solving the woolly mammoth conundrum: amino acid (15)N-enrichment suggests a distinct forage or habitat Schwartz-Narbonne, Rachel Longstaffe, Fred J. Metcalfe, Jessica Z. Zazula, Grant Sci Rep Article Understanding woolly mammoth ecology is key to understanding Pleistocene community dynamics and evaluating the roles of human hunting and climate change in late Quaternary megafaunal extinctions. Previous isotopic studies of mammoths’ diet and physiology have been hampered by the ‘mammoth conundrum’: woolly mammoths have anomalously high collagen δ(15)N values, which are more similar to coeval carnivores than herbivores, and which could imply a distinct diet and (or) habitat, or a physiological adaptation. We analyzed individual amino acids from collagen of adult woolly mammoths and coeval species, and discovered greater  (15)N enrichment in source amino acids of woolly mammoths than in most other herbivores or carnivores. Woolly mammoths consumed an isotopically distinct food source, reflective of extreme aridity, dung fertilization, and (or) plant selection. This dietary signal suggests that woolly mammoths occupied a distinct habitat or forage niche relative to other Pleistocene herbivores. Nature Publishing Group 2015-06-09 /pmc/articles/PMC4460640/ /pubmed/26056037 http://dx.doi.org/10.1038/srep09791 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Schwartz-Narbonne, Rachel
Longstaffe, Fred J.
Metcalfe, Jessica Z.
Zazula, Grant
Solving the woolly mammoth conundrum: amino acid (15)N-enrichment suggests a distinct forage or habitat
title Solving the woolly mammoth conundrum: amino acid (15)N-enrichment suggests a distinct forage or habitat
title_full Solving the woolly mammoth conundrum: amino acid (15)N-enrichment suggests a distinct forage or habitat
title_fullStr Solving the woolly mammoth conundrum: amino acid (15)N-enrichment suggests a distinct forage or habitat
title_full_unstemmed Solving the woolly mammoth conundrum: amino acid (15)N-enrichment suggests a distinct forage or habitat
title_short Solving the woolly mammoth conundrum: amino acid (15)N-enrichment suggests a distinct forage or habitat
title_sort solving the woolly mammoth conundrum: amino acid (15)n-enrichment suggests a distinct forage or habitat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460640/
https://www.ncbi.nlm.nih.gov/pubmed/26056037
http://dx.doi.org/10.1038/srep09791
work_keys_str_mv AT schwartznarbonnerachel solvingthewoollymammothconundrumaminoacid15nenrichmentsuggestsadistinctforageorhabitat
AT longstaffefredj solvingthewoollymammothconundrumaminoacid15nenrichmentsuggestsadistinctforageorhabitat
AT metcalfejessicaz solvingthewoollymammothconundrumaminoacid15nenrichmentsuggestsadistinctforageorhabitat
AT zazulagrant solvingthewoollymammothconundrumaminoacid15nenrichmentsuggestsadistinctforageorhabitat