Abstract
Compound specific isotopic analysis (CSIA) of amino acids has received increasing attention in ecological studies in recent years due to its ability to evaluate trophic positions and elucidate baseline nutrient sources. However, the incorporation rates of individual amino acids into protein and specific trophic discrimination factors (TDFs) are largely unknown, limiting the application of CSIA to trophic studies. We determined nitrogen turnover rates of individual amino acids from a long-term (up to 1054 days) laboratory experiment using captive Pacific bluefin tuna, Thunnus orientalis (PBFT), a large endothermic pelagic fish fed a controlled diet. Small PBFT (white muscle δ15N∼11.5‰) were collected in San Diego, CA and transported to the Tuna Research and Conservation Center (TRCC) where they were fed a controlled diet with high δ15N values relative to PBFT white muscle (diet δ15N∼13.9‰). Half-lives of trophic and source amino acids ranged from 28.6 to 305.4 days and 67.5 to 136.2 days, respectively. The TDF for the weighted mean values of amino acids was 3.0 ‰, ranging from 2.2 to 15.8 ‰ for individual combinations of 6 trophic and 5 source amino acids. Changes in the δ15N values of amino acids across trophic levels are the underlying drivers of the trophic 15N enrichment. Nearly all amino acid δ15N values in this experiment changed exponentially and could be described by a single compartment model. Significant differences in the rate of 15N incorporation were found for source and trophic amino acids both within and between these groups. Varying half-lives of individual amino acids can be applied to migratory organisms as isotopic clocks, determining the length of time an individual has spent in a new environment. These results greatly enhance the ability to interpret compound specific isotope analyses in trophic studies.
Highlights
There are a number of novel tools available to trace nutrient movement through food webs or ecosystems
Analysis of prey items from two time points may not encompass the temporal variability within the diet, it has been shown that the d15N value of source amino acids such as phenylalanine correlates significantly with the d15N values of bulk tissue [8]
The lack of difference in d15N values between initial PBFT white muscle and the mass-weighted mean of the feed meant that turnover could be modeled in only four trophic amino acids (Ala, Leu, Pro, and Val) and four source amino acids (Gly, Lys, Ser, and Thr)
Summary
There are a number of novel tools available to trace nutrient movement through food webs or ecosystems. Amino acid compound specific isotopic analysis (AA-CSIA) has shown distinct potential in elucidating information about both nutrient sources and trophic interactions from a single organism [4,5,6,7,8,9]. Calculations of trophic position from isotopic analysis of bulk tissue require knowledge of baseline isotopic values to correct for spatial and temporal variations in the values of compounds such as NO3, NO2, NH4 and total dissolved inorganic carbon, which are propagated up food webs. The AA-CSIA method allows the calculation of trophic position, and comparisons of source d15N values between similar organisms to evaluate food web and migratory dynamics [5,6,7,8]
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