The diet-body offset in human nitrogen isotopic values: A controlled dietary study
The “trophic level enrichment” between diet and body results in an overall increase in nitrogen isotopic values as the food chain is ascended. Quantifying the diet–body Δ15N spacing has proved difficult, particularly for humans. The value is usually assumed to be +3–5‰ in the archaeological literatu...
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Published in | American journal of physical anthropology Vol. 149; no. 3; pp. 426 - 434 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.11.2012
Wiley-Liss Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | The “trophic level enrichment” between diet and body results in an overall increase in nitrogen isotopic values as the food chain is ascended. Quantifying the diet–body Δ15N spacing has proved difficult, particularly for humans. The value is usually assumed to be +3–5‰ in the archaeological literature. We report here the first (to our knowledge) data from humans on isotopically known diets, comparing dietary intake and a body tissue sample, that of red blood cells. Samples were taken from 11 subjects on controlled diets for a 30‐day period, where the controlled diets were designed to match each individual's habitual diet, thus reducing problems with short‐term changes in diet causing isotopic changes in the body pool. The Δ15Ndiet‐RBC was measured as +3.5‰. Using measured offsets from other studies, we estimate the human Δ15Ndiet‐keratin as +5.0–5.3‰, which is in good agreement with values derived from the two other studies using individual diet records. We also estimate a value for Δ15Ndiet‐collagen of ≈6‰, again in combination with measured offsets from other studies. This value is larger than usually assumed in palaeodietary studies, which suggests that the proportion of animal protein in prehistoric human diet may have often been overestimated in isotopic studies of palaeodiet. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc. |
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Bibliography: | The Wellcome Trust - No. WT074229 ArticleID:AJPA22140 Re-use of this article is permitted in accordance with the Terms and Conditions set out at http://wileyonlinelibrary.com/onlineopen#OnlineOpen_Terms Medical Research Council, World Cancer Research Fund ark:/67375/WNG-PXLMBBG2-F istex:1A6389D3FC1557C667DFC9C7ADAE8C08F75770E1 http://wileyonlinelibrary.com/onlineopen#OnlineOpen_Terms Re‐use of this article is permitted in accordance with the Terms and Conditions set out at ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 14 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 Grant sponsor: The Wellcome Trust; Grant number: WT074229. Grant sponsors: Medical Research Council, World Cancer Research Fund. |
ISSN: | 0002-9483 1096-8644 1096-8644 2692-7691 |
DOI: | 10.1002/ajpa.22140 |