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Insights into amino acid fractionation and incorporation by compound-specific carbon isotope analysis of three-spined sticklebacks

GND
1286782740
Zugehörigkeit
Instrumental Analytical Chemistry, University of Duisburg-Essen, Universitätsstr. 5, Essen, Germany
Hesse, Tobias;
GND
142464325
Zugehörigkeit
Instrumental Analytical Chemistry, University of Duisburg-Essen, Universitätsstr. 5, Essen, Germany
Nachev, Milen;
Zugehörigkeit
Instrumental Analytical Chemistry, University of Duisburg-Essen, Universitätsstr. 5, Essen, Germany
Khaliq, Shaista;
ORCID
0000-0002-1905-9999
Zugehörigkeit
Instrumental Analytical Chemistry, University of Duisburg-Essen, Universitätsstr. 5, Essen, Germany
Jochmann, Maik;
Zugehörigkeit
Institute for Evolution & Biodiversity, University of Münster, Hüfferstr. 1, Münster, Germany
Franke, Frederik;
GND
123707358
ORCID
0000-0003-4291-6853
VIAF
23056131
Zugehörigkeit
Institute for Evolution & Biodiversity, University of Münster, Hüfferstr. 1, Münster, Germany
Scharsack, Jörn Peter;
ORCID
0000-0002-7258-459X
Zugehörigkeit
Institute for Evolution & Biodiversity, University of Münster, Hüfferstr. 1, Münster, Germany
Kurtz, Joachim;
GND
173045731
Zugehörigkeit
Instrumental Analytical Chemistry, University of Duisburg-Essen, Universitätsstr. 5, Essen, Germany
Sures, Bernd;
GND
1074278453
Zugehörigkeit
Instrumental Analytical Chemistry, University of Duisburg-Essen, Universitätsstr. 5, Essen, Germany
Schmidt, Torsten C.

Interpretation of stable isotope data is of upmost importance in ecology to build sound models for the study of animal diets, migration patterns and physiology. However, our understanding of stable isotope fractionation and incorporation into consumer tissues is still limited. We therefore measured the δ13C values of individual amino acids over time from muscle and liver tissue of three-spined sticklebacks (Gasterosteus aculeatus) on a high protein diet. The δ13C values of amino acids in the liver quickly responded to small shifts of under ± 2.0‰ in dietary stable isotope compositions on 30-day intervals. We found on average no trophic fractionation in pooled essential (muscle, liver) and non-essential (muscle) amino acids. Negative Δδ13C values of − 0.7 ± 1.3‰ were observed for pooled non-essential (liver) amino acids and might indicate biosynthesis from small amounts of dietary lipids. Trophic fractionation of individual amino acids is reported and discussed, including unusual Δδ13C values of over + 4.9 ± 1.4‰ for histidine. Arginine and lysine showed the lowest trophic fractionation on individual sampling days and might be useful proxies for dietary sources on short time scales. We suggest further investigations using isotopically enriched materials to facilitate the correct interpretation of ecological field data.

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