Influence of Solvent Lipid Extraction on Tissue‐Specific Carbon Isotopes

Cetacean blubber and skin have a high lipid content, which is depleted in 13 C and 15 N compared to proteins. As such, it is necessary to normalise samples for lipids prior to bulk stable isotope analysis. This is often achieved via solvent lipid removal. The direct effects of solvents used in lipid extractions on δ 15 N of animal tissue is a widely discussed topic in the fields of stable isotope and cetacean trophic ecology. The effects of such solvents on δ 13 C on the other hand, beyond the desired effect of lipid removal, have not yet been studied, although outcomes may be as unpredictable as those found for δ 15 N. Here, we evaluate the effects of solvent lipid extraction on four pure proteins, as well as humpback whale blubber tissue. Lipids were extracted multiple times prior to stable isotope analysis, which also served to demonstrate the efficiency of each lipid extraction cycle. Our results showed that the solvents used, dichloromethane and methanol, did not have a significant effect on δ 13 C and δ 15 N of pure protein as values largely remained within 0.5‰ of unextracted samples, which is equivalent to the expected analytical error. Humpback whale blubber δ 13 C, on the other hand, increased significantly with each lipid extraction cycle, and C:N ratios were only equivalent to those of pure protein, 2.87, after three lipid extractions. These results highlight that solvent lipid extraction has no effect on δ 13 C beyond the desired effect of lipid removal but that gentle lipid extraction protocols are inefficient and that multiple lipid extraction cycles are required to achieve robust isotopic measures.