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Quality control for modern bone collagen stable carbon and nitrogen isotope measurements
Author(s) -
Guiry Eric J.,
Szpak Paul
Publication year - 2020
Publication title -
methods in ecology and evolution
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.425
H-Index - 105
ISSN - 2041-210X
DOI - 10.1111/2041-210x.13433
Subject(s) - diagenesis , stable isotope ratio , isotope analysis , chemistry , subfossil , isotope , isotopes of nitrogen , nitrogen , environmental chemistry , mineralogy , biology , paleontology , ecology , organic chemistry , physics , quantum mechanics , holocene
Isotopic analyses of collagen, the main protein preserved in subfossil bone and tooth, has long provided a powerful tool for the reconstruction of ancient diets and environments. Although isotopic studies of contemporary ecosystems have typically focused on more accessible tissues (e.g. muscle, hair), there is growing interest in the potential for analyses of collagen because it is often available in hard tissue archives (e.g. scales, skin, bone, tooth), allowing for enhanced long‐term retrospective studies. The quality of measurements of the stable carbon and nitrogen isotopic compositions of ancient samples is subject to robust and well‐established criteria for detection of contaminants and diagenesis. Among these quality control (QC) criteria, the most widely utilized is the atomic C:N ratio (C:N Atomic ), which for ancient samples has an acceptable range between 2.9 and 3.6. While this QC criterion was developed for ancient materials, it has increasingly being applied to collagen from modern tissues. Here, we use a large survey of published collagen amino acid compositions ( n = 436) from 193 vertebrate species as well as recent experimental isotopic evidence from 413 modern collagen extracts to demonstrate that the C:N Atomic range used for ancient samples is not suitable for assessing collagen quality of modern and archived historical samples. For modern tissues, collagen C:N Atomic falling outside 3.00–3.30 for fish and 3.00–3.28 for mammals and birds can produce systematically skewed isotopic compositions and may lead to significant interpretative errors. These findings are followed by a review of protocols for improving C:N Atomic criteria for modern collagen extracts. Given the tremendous conservation and environmental policy‐informing potential that retrospective isotopic analyses of collagen from contemporary and archived vertebrate tissues have for addressing pressing questions about long‐term environmental conditions and species behaviours, it is critical that QC criteria tailored to modern tissues are established.