Dear Colleagues,

We are pleased to announce the publication of the following article in the 
journal MEPS. 

Effect of phylogeny and prey type on fatty acid calibration coefficients in 
three species of pinnipeds – implications for the QFASA dietary quantification 
technique

David A.S. Rosen and Dominic J. Tollit 

Marine Ecology Progress Series 467, 263-276.

doi:10.3354/meps09934


Abstract
Quantitative fatty acid signature analysis (QFASA) has been proposed as a 
technique for determining the long-term diet of animals. The method compares 
the fatty acid (FA) profiles of predators and potential prey items to estimate 
relative prey intake. We tested the assumptions of a key step in QFASA, the 
correction of predator FA signatures for metabolic processes through sets of 
calibration coefficients (CCs). We conducted long-term controlled feeding 
studies with captive Steller sea lions consuming herring and eulachon and 
northern fur seals consuming herring. We compared the results with data from 
harbour seals eating herring to evaluate the effects of phylogeny and prey type 
on individual CCs. Even within the limited extended dietary FA subset 
recommended for use by other researchers, we found that at least 41% of the CCs 
differed by family (otariid vs. phocid seals) and 58% differed by predator 
species (sea lion vs. fur seal), suggesting that CCs may be highly 
species-specific. We also found that 64% of the CCs differed by prey type (sea 
lions consuming herring vs. eulachon), which raises some fundamental 
implementation issues. We also found significant differences in diet 
predictions when the herring- and eulachon-derived sets of CCs were applied to 
an actual multi-species diet. CCs are presently used as a simple mathematical 
attempt to describe potentially complex biochemistry. The results of this study 
raise questions regarding the validity of using CCs derived from an alternative 
predator species, and highlight some fundamental issues regarding QFASA 
methodology that need to be addressed through further controlled studies.




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