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Behavioral Responses of the Invasive Halyomorpha halys (StAyenl) to Traps Baited with Stereoisomeric Mixtures of 10,11-Epoxy-1-bisabolen-3-OL

Authors
Leskey, Tracy C.Khrimian, AshotWeber, Donald C.Aldrich, Jeffrey C.Short, Brent D.Lee, Doo-HyungMorrison, William R., III
Issue Date
Apr-2015
Publisher
SPRINGER
Keywords
Semiochemicals; Behavior; Halyomorpha halys; Monitoring; Integrated pest management; Aggregation pheromones; Hemiptera; Pentatomidae; Invasive pest
Citation
JOURNAL OF CHEMICAL ECOLOGY, v.41, no.4, pp.418 - 429
Journal Title
JOURNAL OF CHEMICAL ECOLOGY
Volume
41
Number
4
Start Page
418
End Page
429
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/10670
DOI
10.1007/s10886-015-0566-x
ISSN
0098-0331
Abstract
The brown marmorated stink bug, Halyomorpha halys, is an invasive insect in the United States that is capable of inflicting significant yield losses for fruit, vegetable, and soybean growers. Recently, a male-produced aggregation pheromone of H. halys was identified as a 3.5:1 mixture of (3S,6S,7R,10S)-10,11-epoxy-1-bisabolen-3-ol and (3R,6S,7R,10S)-10,11-epoxy-1-bisabolen-3-ol, two stereoisomers of a natural sesquiterpene with a bisabolane skeleton, potentially existing in 16 stereoisomeric forms. In this study, we assessed attraction to pheromonal and non-pheromonal stereoisomeric mixtures of 10,11-epoxy-1-bisabolen-3-ol, which are easier to synthesize than single isomers, and evaluated dose-dependent responses to attractive mixtures in field trials. Some treatments not containing the natural pheromone components were moderately active in field-trapping studies, signifying that some stereoisomers of 10,11-epoxy-1-bisabolen-3-ol are sufficiently similar to the true pheromone in structure to trigger behavioral responses. Importantly, we found that mixtures of stereoisomers containing pheromone components were also highly attractive to H. halys, even in the presence of multiple "unnatural" stereoisomers. Further, adult and nymphal captures were dose-dependent, regardless of whether the lure contained pheromonal or non-pheromonal components. Our findings of attraction to pheromonal and non-pheromonal stereoisomers and lack of inhibition from non-pheromonal stereoisomers of 10,11-epoxy-1-bisabolen-3-ol increase the flexibility of developing pheromone-based products for H. halys.
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