Preservation of fatty acid signatures in three vertebrate species after six months of storage at various temperatures

• Published in: PloS one Vol. 13; no. 9; p. e0204207
• Main Authors: Nieminen, Petteri, Käkelä, Reijo, Mäkinen, Tero, Laine, Olli, Takalo, Teemu, Mustonen, Anne-Mari
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 17.09.2018; Public Library of Science (PLoS)
• Subjects: Autolysis; Autopsy; Autoxidation; Biology and Life Sciences; Biopsy; Discriminant analysis; Ecological monitoring; Ecology; Enzymatic activity; Enzymes; Fatty acids; Fish; Foraging behavior; Freezing; Freezing temperatures; Health sciences; Lipids; Medicine; Oncorhynchus mykiss; Oxygen; Physical Sciences; Preservation; Research and Analysis Methods; Sampling; Signatures; Species; Storage; Storage temperature; Sturgeon; Temperature; Temperature effects; Trout; Wild animals; Baltic Sea; Finland
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0204207

Fatty acid (FA) signatures (FAS) are important tools to assess the foraging ecology of wild animals. The present study was conducted to assess how well the general FAS and the proportions of individual FA are preserved in fat samples stored at different temperatures (-196, -80, -20, +4 and +20°C). Using three species (laboratory rat, American mink and rainbow trout), FAS were determined immediately upon sampling. Thereafter, eight subsamples per storage temperature from the inner part of the sample unaffected by oxygen and light were re-analyzed after 1, 2, 3, 7, 28, 84 and 168 days. Each time the remaining sample was sealed in its vial after replacing air with nitrogen gas. The results were tested with the mixed model and discriminant analyses. Generally, the FAS were well preserved regardless of storage temperature, and only a few major FA showed significant changes even after the 6-month period at room temperature. After an initial first-day change in proportions, presumably due to post-mortem enzymatic activities, the remaining minor changes could not be clearly attributed to either further autolysis, decomposition or autoxidation. In the discriminant analysis, the species-specific differences dominated and remained distinct even after 6 months. Furthermore, the analysis mostly classified the samples preserved at sub- and above-freezing temperatures separate from each other, and the general deviation from the initial analysis results was present as early as after 1 day. If FAS are to be analyzed in a very precise manner, the analysis should be performed immediately upon sampling. However, FAS remain adequately reliable for long periods of time even without preservation in deep freeze, widening the availability of potential samples for studies on foraging ecology and related disciplines.