Abstract
Volatile compounds in the lipid coating of the lower-back quills of the North American porcupine,Erethizon dorsatum, were collected using headspace trapping on Tenax and analyzed by gas chromatography–mass spectrometry (GC-MS), GC with organoleptic detection, and GC with a chiral stationary phase. Over 50 components were isolated, primarily oxygenated aliphatics, lactones, and isoprenoids. The most abundant constituent was tetradecyl acetate, which does not contribute significantly to the odor of the quill lipids. GC with a wide-bore capillary column and a human nose as detector was used to determine the retention time of the peak with the characteristic porcupine odor. Comparison of this organoleptic chromatogram with those obtained with a flame ionization detector and GC-MS showed the compound to be a δ-decalactone. The racemic mixture of this optically active substance does not possess the unique odor. Resolution of the enantiomers of δ-decalactone by GC with a chiral cyclodextrin phase shows that the isomer possessing the characteristic porcupine odor is the(R)-δ-decalactone. We suggest the biological function of this compound is to serve as a warning odor, which, in conjunction with an initial quill strike, produces a conditioned aversion in potential predators.
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Li, G., Roze, U. & Locke, D.C. Warning Odor of the North American Porcupine(Erethizon dorsatum). J Chem Ecol 23, 2737–2754 (1997). https://doi.org/10.1023/A:1022511026529
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DOI: https://doi.org/10.1023/A:1022511026529