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Potential for semiochemical-based monitoring of the pea leaf weevil (Coleoptera: Curculionidae) on field pea (Fabaceae) in the Canadian Prairie Provinces

Published online by Cambridge University Press:  15 March 2016

M.L. Evenden ,
C.M. Whitehouse ,
A. St. Onge ,
L. Vanderark ,
J.-P. Lafontaine ,
S. Meers  and
H.A. Cárcamo
M.L. Evenden*
Affiliation:
Department of Biological Sciences, University of Alberta, Edmonton, Alberta, T6G 2E9, Canada
C.M. Whitehouse
Affiliation:
Forest Health and Adaptation, Forest Management Branch, Alberta Agriculture and Forestry, Edmonton, Alberta, T5K 2M4, Canada
A. St. Onge
Affiliation:
Department of Biological Sciences, University of Alberta, Edmonton, Alberta, T6G 2E9, Canada
L. Vanderark
Affiliation:
Scotts Canada Ltd., Delta, British Columbia, V4G IE9, Canada
J.-P. Lafontaine
Affiliation:
Scotts Canada Ltd., Delta, British Columbia, V4G IE9, Canada
S. Meers
Affiliation:
Pest Surveillance Branch, Alberta Agriculture and Forestry, Brooks, Alberta, T1R 1E6, Canada
H.A. Cárcamo
Affiliation:
Agriculture and Agri-Food Canada, Lethbridge Research Centre, Lethbridge, Alberta, T1J 4B1, Canada
*
1Corresponding author (e-mail: mevenden@ualberta.ca).
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Abstract

The pea leaf weevil, Sitona lineatus (Linnaeus) (Coleoptera: Curculionidae), is an important pest of field peas, Pisum sativum Linnaeus (Fabaceae), and faba beans, Vicia faba Linnaeus (Fabaceae), that has recently become established in the Prairie Provinces of Canada. Male pea leaf weevils produce an aggregation pheromone, 4-methyl-3,5-heptanedione, in the spring when overwintered weevils migrate to fields to feed and mate. The current study tests the attractiveness of the aggregation pheromone with and without synthetic bean volatiles to pea leaf weevils in the spring and in the fall when weevils seek perennial legumes to feed and overwinter. Modified Leggett traps similar to those used in Europe did not retain weevils in this study. Aggregation pheromone-baited pitfall traps caught male and female weevils in the spring and fall. Weevils were not attracted to traps baited with three bean volatiles, (Z)-3-hexen-1-yl acetate, (Z)-3-hexen-1-ol, and linalool. Bean volatiles did enhance response to pheromone, but only in the fall. Weevils were captured in most semiochemical-baited traps in a 1:1 sex ratio, but female-biased catch in control traps might indicate greater activity of females in the trap vicinity. This study lays the groundwork for semiochemical-based monitoring to detect pea leaf weevil spread in the Prairie Provinces.

Type
Insect Management
Information
The Canadian Entomologist , Volume 148 , Issue 5 , October 2016 , pp. 595 - 602
Copyright
© Entomological Society of Canada 2016 

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Footnotes

Subject editor: Jon Sweeney

References

Adams, J.T. and Hauser, C.R. 1944. The acylation of methyl ketones with aliphatic esters by means of sodium amide. Synthesis of β-diketones of the type RCOCH2COR1. Journal of American Chemical Society, 66: 1220–1222.Google Scholar
Blight, M.M., Pickett, J.A., Smith, M.C., and Wadhams, L.J. 1984. An aggregation pheromone of Sitona lineatus . Naturwissenschaften, 71: 480.CrossRefGoogle Scholar
Blight, M.M. and Wadhams, L.J. 1987. Male-produced aggregation pheromone in pea and bean weevil, Sitona lineatus (L.). Journal of Chemical Ecology, 13: 733–739.Google Scholar
Fisher, J.R. and O’Keeffe, L.E. 1979. Seasonal migration and flight of the pea leaf weevil, Sitona lineatus (Coleoptera: Curculionidae) in northern Idaho and eastern Washington. Entomologia Experimentalis et Applicata, 26: 189–196.Google Scholar
George, K.S. 1962. Root nodule damage by larvae of Sitona lineatus and its effect on yield of green peas. Plant Pathology, 11: 172–176.Google Scholar
Hamon, N., Bardner, R., Allen-Williams, L., and Lee, J.B. 1987. Flight periodicity and infestation size of Sitona lineatus . Annals of Applied Biology, 111: 271–284.Google Scholar
Jackson, D.J. 1919. Bionomics of weevils of the genus Sitones injurious to leguminous crops in Britain. Annals of Biology, 7: 269–297.Google Scholar
Kalaitzakis, D., Rozzell, J.D., Kambourakis, S., and Smonou, I. 2006. A two-step chemoenzymatic synthesis of the natural pheromone (+-sitophilure utilizing isolated, NADPH-dependent ketoreductases. European Journal of Organic Chemistry, 2006: 2309–2313.Google Scholar
Landon, F., Ferary, S., Pierre, D., Auger, J., Biemont, J.C., Levieux, J., and Pouzat, J. 1997. Sitona lineatus host-plant odors and their components: effect on locomotor behavior and peripheral sensitivity variations. Journal of Chemical Ecology, 23: 2161–2173.Google Scholar
Leggett, L.E., Cross, W.H., Mitchell, H.C., Johnson, W.L., and McGovern, W.L. 1975. Improved traps for capturing boll weevils. Journal of the Georgia Entomological Society, 10: 52–61.Google Scholar
Light, D.M., Flath, R.A., Buttery, R.G., Zalom, F.G., Rice, R.E., Dickens, J.C., and Jang, E.B. 1993. Host-plant green-leaf volatiles synergize sex pheromones of the corn earworm and codling moth (Lepidoptera). Chemoecology, 4: 145–152.Google Scholar
Miluch, C.E., Dosdall, L.M., and Evenden, M.L. 2014. Factors influencing male Plutella xylostella (Lepidoptera: Plutellidae) capture rates in sex pheromone-baited traps on canola in western Canada. Journal of Economic Entomology, 107: 2067–2076.Google Scholar
Nielsen, B.S. and Jensen, T.S. 1993. Spring dispersal of Sitona lineatus: the use of aggregation pheromone traps for monitoring. Entomologia Experimentalis et Applicata, 66: 21–30.CrossRefGoogle Scholar
Pureswaran, D.S. and Borden, J.H. 2005. Primary attraction and kairomonal host discrimination in three species of Dendroctonus (Coleoptera: Scolytidae). Agricultural and Forest Entomology, 7: 219–230.Google Scholar
R Core Team. 2015. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. Available from http://www.R-project.org [accessed 29 January 2016].Google Scholar
Reddy, G.V.P. and Guerrero, A. 2000. Behavioral responses of the diamondback moth, Plutella xylostella, to green leaf volatiles of Brassica oleracea subsp. capitata . Journal of Agriculture Food Chemistry, 48: 6025–6029.CrossRefGoogle ScholarPubMed
Schotzko, D.J. and O’Keeffe, L.E. 1986. Reproductive system maturation and changes in flight muscles of female pea leaf weevils (Coleoptera: Curculionidae). Annals of the Entomological Society of America, 79: 109–111.Google Scholar
Vankosky, M.A., Cárcamo, H.A., and Dosdall, L.M. 2011. Response of Pisum sativum (Fabales: Fabaceae) to Sitona lineatus (Coleoptera: Curculionidae) infestation: effect of adult weevil density on damage, larval population, and yield loss. Journal of Economic Entomology, 104: 1550–1560.CrossRefGoogle ScholarPubMed
Vankosky, M.A., Dosdall, L.M., and Cárcamo, H.A. 2009. Distribution, biology and integrated management of the pea leaf weevil, Sitona lineatus L. (Coleoptera: Curculionidae), with an analysis of research needs. CAB Reviews: Perspectives in Agriculture, Veterinary Science, Nutrition and Natural Resources, 4: 1–18.Google Scholar