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Woods Hole Oceanographic Institution

Kelton McMahon

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Publications
»Ocean Ecogeochemistry
»Estimating movement of marine animals
»Functional connectivity in a coral reef seascape
»Carbon isotopes identify snapper nursery habitat
»Otolith amino acid carbon isotope method
»Amino acid fractionation in fish tissues
»Stable isotope fractionation in fish muscle and otoliths
»Transequatorial Migrations by Basking Sharks
»Tracking top predator migration with isoscapes
»Bivalves as bioproxies for climate change
»Serries groenlandicus
»Digestibility of Ice algae and Phytoplankton
»Salt marsh fish movement and trophic dynamics


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Kelton W. McMahon, Marilyn L. Fogel, Travis S. Elsdon, Simon R. Thorrold, Carbon isotope fractionation of amino acids in fish muscle reflects biosynthesis and isotopic routing from dietary protein., Journal of Animal Ecology 79:1132-1141, 2010

1. Analysis of stable carbon isotopes is a valuable tool for studies of diet, habitat use, and migration.  However, significant variability in the degree of trophic fractionation (∆13CC-D) between consumer (C) and diet (D) has highlighted our lack of understanding of the biochemical and physiological underpinnings of stable isotope ratios in tissues.

2. An opportunity now exists to increase the specificity of dietary studies by analyzing the δ13C values of amino acids (AAs).  Common mummichogs (Fundulus heteroclitus, Linnaeus 1766) were reared on four isotopically distinct diets to examine individual AA ∆13CC-D variability in fish muscle. 

3. Modest bulk tissue ∆13CC-D values reflected relatively large trophic fractionation for many non-essential AAs and little to no fractionation for all essential AAs. 

4. Essential AA d13C values were not significantly different between diet and consumer (∆13CC-D = 0.0 ± 0.4‰), making them ideal tracers of carbon sources at the base of the food web.  Stable isotope analysis of muscle essential AAs provides a promising tool for dietary reconstruction and identifying baseline d13C values to track animal movement through isotopically distinct food webs.

5. Non-essential AA ∆13CC-D values showed evidence of both de novo biosynthesis and direct isotopic routing from dietary protein.  We attributed patterns in ∆13CC-D to variability in protein content and AA composition of the diet as well as differential utilization of dietary constituents contributing to the bulk carbon pool.  This variability illustrates the complicated nature of metabolism and suggests caution must be taken with the assumptions used to interpret bulk stable isotope data in dietary studies. 

6. Our study is the first to investigate the expression of AA ∆13CC-D values for a marine vertebrate and should provide for significant refinements in studies of diet, habitat use, and migration using stable isotopes.

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