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- Bäckman, A. C., et al.
(författare)
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Antennal response of codling moth males, Cydia pomonella L. (Lepidoptera: Tortricidae), to the geometric isomers of codlemone and codlemone acetate
- 2000
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Ingår i: Journal of Comparative Physiology A. Sensory, neural, and behavioral physiology. - : Springer. - 0340-7594 .- 1432-1351. ; 186:6, s. 513-519
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Tidskriftsartikel (refereegranskat)abstract
- Single sensillum recordings from Cydia pomonella male antennae showed three different types of receptor neurons. The most abundant type was most sensitive to the main pheromone compound (E,E)-8,10-dodecadienol, while its response to the geometric isomers E,Z, Z,E and Z,Z was comparable to a tenfold lower dose of (E,E)-8,10-dodecadienol. This neuron type also responded to the four behaviorally antagonistic isomers of (Delta,Delta)-8,10-dodecadienyl acetate, among which it was most sensitive to the E,E isomer. Cross-adaptation studies showed that these compounds were all detected by the same receptor neuron type. Receptor neurons specifically tuned to (E,Z) or (Z,Z)-8,10-dodecadienol were not found, although these two compounds are behaviorally active. A second type of receptor neuron responded to all isomers of (Delta,Delta)-8,10-dodecadienyl acetate and was most sensitive to the E,E isomer. This neuron type did not respond to any of the isomers of (Delta,Delta)-8,10-dodecadienol. A third receptor neuron type was highly sensitive to the plant compound alpha-farnesene. The finding that the receptor neuron type tuned to the main pheromone compound responded even to strong behavioral antagonists aids the interpretation of ongoing behavioral studies for the development of the mating disruption technique in codling moth.
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| 2. |
- Witzgall, P., et al.
(författare)
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Attraction of Pea Moth Cydia-Nigricana F (Lepidoptera, Tortricidae) to Female Sex-Pheromone (E,E)-8,10-Dodecadien-1-Yl Acetate, Is Inhibited by Geometric Isomers E,Z, Z,E, and Z,Z
- 1993
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Ingår i: Journal of Chemical Ecology. - 0098-0331 .- 1573-1561. ; 19:9, s. 1917-1928
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Tidskriftsartikel (refereegranskat)abstract
- Field attraction of Cydia nigricana males to synthetic female sex pheromone (E,E)-8,10-dodecadien-1-yl acetate, formulated on red rubber septa, declined continuously during two weeks. This was due to isomerization of (E,E)-8, 10-dodecadien-1-yl acetate: eight days after application of purified E,E isomer, the proportion of E,Z; Z,E; and Z,Z isomers in rubber septa aged in the laboratory was 4 %; a 5 % addition of any one of these isomers to fresh lures of (E,E)-8, 10-dodecadien-1-yl acetate significantly reduced male attraction. Stereospecific syntheses of (E,Z)-, (Z,E)-, and (Z,Z)-g, 10-dodecadien-1-yl acetate are described. The pheromone gland of Cydia nigricana contains 0.8 ng/female of (E,E)-8,10-dodecadien-1-yl acetate, accompanied by three monounsaturated acetates, (E)-9-dodecen-1-yl acetate, (Z)-5-tetradecen-1-yl acetate, and (Z)-7-tetradecen-1-yl acetate (0.1 ng/female each). These compounds did not augment male trap catch when added to (E,E)-8,10-dodecadien-1-yl acetate.
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