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- Witzgall, Peter, et al.
(författare)
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Sex pheromones and attractants in the Eucosmini and Grapholitini (Lepidoptera, Tortricidae)
- 1996
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Ingår i: Chemoecology. - : Springer. - 0937-7409 .- 1423-0445. ; 7:1, s. 13-23
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Tidskriftsartikel (refereegranskat)abstract
- The geometric isomers (E, E)-, (E, Z)-, (Z, E)-, and (Z, Z)-8, 10-dodecadien-1-yl acetate were identified as sex pheromone components or sex attractants in the tribes Eucosmini and Grapholitini of the tortricid subfamily Olethreutinae. Species belonging to the more ancestral Tortricinae were not attracted. Each one isomer was behaviourally active in males of Cydia and Grapholita (Grapholitini), either as main pheromone compound, attraction synergist or attraction inhibitor. Their reciprocal attractive/antagonistic activity in a number of species enables specific communication with these four compounds. Pammene, as well as other Grapholita and Cydia responded to the monoenic 8- or 10-dodecen-1-yl acetates. Of the tribes Olethreutini and Eucosmini, Hedya, Epiblema, Eucosma, and Notocelia trimaculana were also attracted to 8, 10-dodecadien-1-yl acetates, but several other Notocelia to 10, 12-tetradecadien-1-yl acetates. The female sex pheromones of C. fagiglandana, C. pyrivora, C. splendana, Epiblema foenella and Notocelia roborana were identified. (E, E)- and (E, Z)- 8, 10-dodecadien-1-yl acetate are produced via a common E9 desaturation pathway in C. splendana. Calling C. nigricana and C. fagiglandana females are attracted to wingfanning males.
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- Zhao, Cheng Hua, et al.
(författare)
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Substrate specificity of acetyltransferase and reductase enzyme systems used in pheromone biosynthesis by Asian corn borer, Ostrinia furnacalis
- 1995
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Ingår i: Journal of Chemical Ecology. - 0098-0331. ; 21:10, s. 1495-1510
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Tidskriftsartikel (refereegranskat)abstract
- The substrate specificity of the acetyltransferase and the reductase enzyme systems used by Ostrinia furnacalis (Lepidoptera: Pyralidae) in pheromone biosynthesis was studied in vivo by topical application of precursors to pheromone glands. Each of the tetradecenols, varying in double bond position (from 7 to 13) and geometry of the double bond, was converted to the corresponding acetate by the acetyltransferase. The similarity in the conversion rates of all tested fatty alcohols indicated that the acetyltransferase has a low substrate specificity. Most of the corresponding tetradecenoic acids could also be converted to the respective acetates. However, very different conversion rates among the tested fatty acids demonstrated that the reductase system has a higher substrate specificity than the acetyltransferase. The conversion rates of most E isomers were higher than those of the corresponding Z isomers, except for the (Δ)-11-tetradecenoic acids, in which much more Z isomer was converted to the product. Saturated tetradecanoic acid was converted to the corresponding acetate at a high rate; the shorter homolog, tridecanoic acid, was converted at a lower rate (56%), and conversion to the respective acetates of the longer homolog, pentadecanoic and hexadecanoic acids, was insignificant (<5%). The results from the present study showed that specificity of pheromone production is to a large extent controlled by the pheromone gland reductase system.
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