Intrapopulation Variability Shaping Isotope Discrimination and Turnover: Experimental Evidence in Arctic Foxes

Background: Tissue-specific stable isotope signatures can provide insights into the trophic ecology of consumers and their roles in food webs. Two parameters are central for making valid inferences based on stable isotopes, isotopic discrimination (difference in isotopic ratio between consumer and i...

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Bibliographic Details
Main Authors: Nicolas Lecomte, Øystein Ahlstrøm, Dorothée Ehrich, Eva Fuglei, Rolf A. Ims, Nigel G. Yoccoz
Other Authors: The Pennsylvania State University CiteSeerX Archives
Format: Text
Language:English
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Online Access:http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.290.7047
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Summary:Background: Tissue-specific stable isotope signatures can provide insights into the trophic ecology of consumers and their roles in food webs. Two parameters are central for making valid inferences based on stable isotopes, isotopic discrimination (difference in isotopic ratio between consumer and its diet) and turnover time (renewal process of molecules in a given tissue usually measured when half of the tissue composition has changed). We investigated simultaneously the effects of age, sex, and diet types on the variation of discrimination and half-life in nitrogen and carbon stable isotopes (d 15 N and d 13 C, respectively) in five tissues (blood cells, plasma, muscle, liver, nail, and hair) of a top predator, the arctic fox Vulpes lagopus. Methodology/Principal Findings: We fed 40 farmed foxes (equal numbers of adults and yearlings of both sexes) with diet capturing the range of resources used by their wild counterparts. We found that, for a single species, six tissues, and three diet types, the range of discrimination values can be almost as large as what is known at the scale of the whole mammalian or avian class. Discrimination varied depending on sex, age, tissue, and diet types, ranging from 0.3 % to 5.3 % (mean = 2.6%) for d 15 N and from 0.2 % to 2.9 % (mean = 0.9%) for d 13 C. We also found an impact of population structure on d 15 N half-life in blood cells. Varying across individuals, d 15 N half-life in plasma (6 to 10 days) was also shorter than for d 13 C (14 to 22 days), though d 15 N and d 13 C half-lives are usually considered as equal.