Killer whale fecal samples: How to get the most out of a single extraction

•Steroid hormones are detectable in methanol residues from lipid extractions.•Hormone concentrations in methanol residues reflect physiological state.•One extraction protocol can be applied for both lipid and hormone analyses.•Linear equations were used to correct for differences in extraction metho...

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Bibliographic Details
Published in:General and comparative endocrinology 2024-08, Vol.354, p.114544, Article 114544
Main Authors: Melica, V., Thornton, S.J.
Format: Article
Language:English
Subjects:
Animals
Corticosterone - analysis
Corticosterone - metabolism
Fecal hormones
Fecal lipids
Feces - chemistry
Female
Hormone extraction
Killer whale
Lipid extraction
Lipids - analysis
Progesterone - analysis
Progesterone - metabolism
Whale, Killer - metabolism
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Summary:•Steroid hormones are detectable in methanol residues from lipid extractions.•Hormone concentrations in methanol residues reflect physiological state.•One extraction protocol can be applied for both lipid and hormone analyses.•Linear equations were used to correct for differences in extraction methodologies. Fecal samples are a non-invasive and relatively accessible matrix for investigating physiological processes in resident killer whale (Orcinus orca) populations. The high lipid content of the diet (primarily salmonids) leads to lower density fecal material and slower dispersion, facilitating sample collection. As fecal discharge is relatively infrequent and the volume of sample is variable, maximizing analytical options is an important consideration. Here we present an extraction methodology to measure hormones and lipid content from the same fecal aliquot. Lipid extractions are commonly conducted using chloroform and methanol from Folch or Bligh and Dyer (B&D), while alcohol is the primary solvent for hormone extraction. We evaluated the possibility of using the methanol layer from lipid extractions to assess fecal steroid hormone levels. Folch and B&D methanol residues were assayed form metabolites of progesterone (PMs) and corticosterone (GCs), and results were compared to aliquots extracted in 70 % ethanol. Hormone concentrations measured in the methanol layer from Folch and B&D extractions were 55 % to 79 % lower than concentrations in 70 % ethanol. We developed mathematical corrections, using linear regression models fitted to Folch or B&D methanol vs 70 % ethanol hormone concentrations (p 
ISSN:0016-6480
1095-6840
1095-6840
DOI:10.1016/j.ygcen.2024.114544