Abstract
AbstractFactors affecting the extraction and bioassay of the sex pheromone of white-marked tussock moths were evaluated. Dipping the female pheromone glands in a solvent (preferably hexane) to produce a wash containing active material was a particularly effective and reproducible method of obtaining a potent extract. These were most active if obtained from virgin females < 2 days old. Extracts from recently mated females were only slightly less active than those from virgin females. Males were most responsive in bioassays when 2 to 3 days old. The maximum percentage response of males was obtained at 1 × 10−4 FE (female equivalents); beyond this concentration the percentage response decreased. Characteristically, extracts lost their potency within 1–3 weeks of preparation. It is suggested that either an inhibitor or loss of a chemical component of the sex pheromone causes an extract to become inactive.
Publisher
Cambridge University Press (CUP)
Subject
Insect Science,Molecular Biology,Physiology,Ecology, Evolution, Behavior and Systematics,Structural Biology
Cited by
16 articles.
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4. (Z,Z)-6,9-heneicosadien-11-one, labile sex pheromone of the whitemarked tussock moth, Orgyia leucostigma;Journal of Chemical Ecology;2003
5. Location of the pheromone producing gland in the European grapevine moth, Lobesia botrana (Lepidoptera : Tortricidae);Applied Entomology and Zoology;1998