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1.
J Chem Ecol ; 20(1): 1-8, 1994 Jan.
Article in English | MEDLINE | ID: mdl-24241694

ABSTRACT

(E)-11,13-Tetradecadienal (E11,13-14:Ald) is the major sex pheromone component of the eastern blackheaded budworm (EBB),Acleris variana (Fern.). The compound was identified in female pheromone gland extracts by coupled gas chromatographic-electroantennographic detection (GC-EAD), coupled GC-mass spectrometry in selected ion monitoring mode, and retention index calculations of candidate pheromone components.E11,13-14:Ald alone as trap bait was very attractive to male EBB. Addition of the corresponding diene alcohol or acetate or both did not enhance attraction. (Z)-11,13-Tetradecadienal in binary combination with (E)-11,13-14:Ald neither enhanced nor reduced trap catches. Increasing the amounts of pheromone from 0.01 to 10 µg increased trap catches, but increase of pheromone quantity above 100 µg proportionately reduced attraction. Stabilization of slowly polymerizingE11,13-14:Ald and development of a sustained, adequate release rate is required for pheromone-based monitoring of EBB populations.

2.
J Chem Ecol ; 19(5): 1009-19, 1993 May.
Article in English | MEDLINE | ID: mdl-24249080

ABSTRACT

The sex pheromone of the western hemlock looper (WHL),Lambdina fiscellaria lugubrosa (Hulst), comprises three methylated hydrocarbons: 5,11-dimethylheptadecane (5,11), 2,5-dimethylheptadecane (2,5), and 7-methylheptadecane (7). Compounds extracted from female pheromone glands were identified by coupled gas chromatographic-electroantennographic (GC-EAD) analysis and coupled GC-mass spectroscopy in selected ion monitoring mode. In trapping experiments, (5,11) alone attracted male moths, but addition of either (7) or (2,5) significantly enhanced attraction. (5,11) combined with both (7) and (2,5) was significantly most attractive. (5,11) and (2,5) are also sex pheromone components of the eastern hemlock looper (EHL),Lambdina fiscellaria fiscellaria (Guen.). Although (7) is produced by the EHL, it is a pheromone component only in the WHL. It constitutes the first behaviorally active monomethyl-branched hydrocarbon to be found in a geometrid and is a novel lepidopteran sex pheromone component. The different 2- versus 3-component sex pheromone supports taxonomic division of EHL and WHL.

3.
J Chem Ecol ; 19(6): 1057-62, 1993 Jun.
Article in English | MEDLINE | ID: mdl-24249125

ABSTRACT

Of the four possible stereoisomers of 5,11-dimethylheptadecane, the major sex pheromone component of the eastern hemlock looper (EHL),Lambdina fiscellaria fiscellaria Guen., and the western hemlock looper (WHL),Lambdina fiscellaria lugubrosa Hulst, (5R,11S)-5,11-dimethylheptadecane was the only stereoisomer eliciting electrophysiological responses by male EHL and WHL antennae. In field bioassays with EHL and WHL populations, traps baited with (5R,11S)-5, 11-dimethylheptadecane caught as many males as did traps baited with all four stereoisomers combined or a synthetic mixture of 5,11-dimethylheptadecanes. Catches in traps baited with the other three stereoisomers did not significantly differ from those in the unbaited control traps. We conclude that male antennae lack chemoreceptors for the other three stereoisomers of 5,11-dimethylheptadecane and hypothesize that only (5R,115)-5,11-dimethylheptadecane is produced by female EHLs and WHLs.

4.
J Chem Ecol ; 17(10): 1989-2002, 1991 Oct.
Article in English | MEDLINE | ID: mdl-24258493

ABSTRACT

Porapak Q-captured volatiles of malePolygraphus rufipennis (Kirby) boring in black spruce and white spruce from Newfoundland and British Columbia, respectively, contained 3-methyl-3-buten-1-ol. Volatiles from logs in which the males had been joined by females contained the compound in reduced quantities. Hindgut extracts from male and femaleP. rufipennis disclosed no male-specific volatiles, but 3-methyl-3-buten-1-ol was detected in extracts of male-produced frass. The compound was not present in extracts from fresh phloem tissue.P. rufipennis of both sexes responded strongly in the field to traps baited with 3-methyl-3-buten-1-ol released at 4390 µg/day. There was little response to unbaited traps, fresh uninfested black spruce logs, or to 3-methyl-3-buten-1-ol released at lower rates. Combination of 3-methyl-3-buten-1-ol with either one of five terpenes prevalent in black spruce did not enhance beetle catch. Approximately half of 20 black spruce trees baited with 3-methyl-3-buten-1-ol were attacked, compared to 20.0% of 10 unbaited control trees. This new aggregation pheromone could be used to monitor or manageP. rufipennis populations.

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