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A Male-Predominant Cuticular Hydrocarbon, 7-Methyltricosane, is used as a Contact Pheromone in the Western Flower Thrips Frankliniella occidentalis

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Abstract

In a laboratory bioassay, adult female Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae) spent more time near filter paper disks that had been exposed to adult males than near unexposed disks; this effect was not observed on disks exposed to adult females. The response could only partly be explained by the known male-produced aggregation pheromone, neryl (S)-2-methylbutanoate, suggesting the presence of an unknown male-produced compound. In gas chromatography/mass spectrometry analyses, 7-methyltricosane was detected on disks exposed to males, but not on disks exposed to females. Extracts of cuticular lipids also showed relatively large amounts of 7-methyltricosane on males, whereas only trace amounts were found on females and none on larvae. Bioassays of synthetic 7-methyltricosane showed that adults responded only after contact. The response to this compound was clearly different from that to n-tricosane or hexane-only controls. Females that contacted 7-methyltricosane on glass beads stayed in the vicinity and frequently raised the abdomen, a behavior that rejects mating attempts by males. Males stayed in the vicinity and wagged the abdomen sideways, a behavior used in fighting between males. This is the first identification of a contact pheromone in the order Thysanoptera.

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References

  • Ablard, K., Gries, R., Khaskin, G., Schaefer, P. W., and Gries, G. 2012. Does the stereochemistry of methylated cuticular hydrocarbons contribute to mate recognition in the egg parasitoid wasp Ooencyrtus kuvanae? J. Chem. Ecol. 38:1306–1317.

    Article  PubMed  CAS  Google Scholar 

  • Abramson, J. H. 2011. WINPEPI updated: Computer programs for epidemiologists, and their teaching potential. Epidemiol. Perspect. Innov. 8:1–9.

    Article  PubMed  Google Scholar 

  • Bagnères, A.-G. and Blomquist, G. J. 2010. Site of synthesis, mechanism of transport and selective deposition of hydrocarbons, pp. 75–99, in G. J. Blomquist and A.-G. Bagnères (eds.), Insect Hydrocarbons. Cambridge University Press, Cambridge.

    Chapter  Google Scholar 

  • Blomquist, G. J. and Bagnères, A.-G. 2010. Insect Hydrocarbons. Cambridge University Press, Cambridge.

    Book  Google Scholar 

  • Dublon, I. A. N. 2009. The Aggregation Pheromone of the Western Flower Thrips. PhD dissertation, Keele University, UK.

  • El-Ghariani, I. M. and Kirk, W. D. J. 2008. The structure of the male sternal glands of the western flower thrips, Frankliniella occidentalis (Pergande). Acta Phytopathol. Entomol. Hung. 43:257–266.

    Article  Google Scholar 

  • Ellington, C. P. 1980. Wing mechanics and take off preparation of Thrips (Thysanoptera). J. Exp. Biol. 85:129–136.

    Google Scholar 

  • Everaerts, C., Farine, J.-P., Cobb, M., and Ferveur, J.-F. 2010. Drosophila cuticular hydrocarbons revisited: Mating status alters cuticular profiles. PLoS One 5:e9607.

    Article  PubMed  Google Scholar 

  • Gołębiowski, M., Maliński, E., Nawrot, J., Szafranek, J., and Stepnowski, P. 2007. Identification of the cuticular lipid composition of the western flower thrips Frankliniella occidentalis. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 147:288–292.

    Article  PubMed  Google Scholar 

  • Grenacher, S. and Guerin, P. M. 1994. Inadvertent introduction of squalene, cholesterol, and other skin products into a sample. J. Chem. Ecol. 20:3017–3025.

    Article  CAS  Google Scholar 

  • Hamilton, J. G. C., Hall, D. R., and Kirk, W. D. J. 2005. Identification of a male-produced aggregation pheromone in the western flower thrips Frankliniella occidentalis. J. Chem. Ecol. 31:1369–1379.

    Article  PubMed  CAS  Google Scholar 

  • Hedrick, T. L. 2008. Software techniques for two- and three-dimensional kinematic measurements of biological and biomimetic systems. Bioinspir. Biomim. 3:034001.

    Article  PubMed  Google Scholar 

  • Hemptinne, J. L., Lognay, G., and Dixon, A. F. G. 1998. Mate recognition in the two-spot ladybird beetle, Adalia bipunctata: Role of chemical and behavioural cues. J. Insect Physiol. 44:1163–1171.

    Article  CAS  Google Scholar 

  • Howard, R. W. and Blomquist, G. J. 2005. Ecological, behavioral, and biochemical aspects of insect hydrocarbons. Annu. Rev. Entomol. 50:371–393.

    Article  PubMed  CAS  Google Scholar 

  • Jones, T. M. and Hamilton, J. G. C. 1998. A role for pheromones in mate choice in a lekking sandfly. Anim. Behav. 56:891–898.

    Article  PubMed  Google Scholar 

  • Kirk, W. D. J. and Hamilton, J. G. C. 2010. The aggregation pheromones of thrips. (Abstract, IXth International Symposium on Thysanoptera and Tospoviruses, 31 August–4 September, 2009). J. Insect Sci. 10(166):19–20.

  • Kirk, W. D. J. and Terry, L. I. 2003. The spread of the western flower thrips Frankliniella occidentalis (Pergande). Agric. For. Entomol. 5:301–310.

    Article  Google Scholar 

  • Lacaille, F., Hiroi, M., Twele, R., Inoshita, T., Umemoto, D., Manière, G., Marion-Poll, F., Ozaki, M., Francke, W., Cobb, M., Everaerts, C., Tanimura, T., and Ferveur, J.-F. 2007. An inhibitory sex pheromone tastes bitter for Drosophila males. PLoS One 2:e661.

    Article  PubMed  Google Scholar 

  • Lewis, T. 1997. Thrips as Crop Pests. CAB International, Wallingford.

    Google Scholar 

  • Macdonald, K. M., Hamilton, J. G. C., Jacobson, R., and Kirk, W. D. J. 2003. Analysis of anal droplets of the western flower thrips Frankliniella occidentalis. J. Chem. Ecol. 29:2385–2389.

    Article  PubMed  CAS  Google Scholar 

  • Mound, L. A. 2009. Sternal pore plates (glandular areas) of male Thripidae (Thysanoptera). Zootaxa 2129:29–46.

    Google Scholar 

  • Rutledge, C. E., Millar, J. G., Romero, C. M., and Hanks, L. M. 2009. Identification of an important component of the contact sex pheromone of Callidiellum rufipenne (Coleoptera: Cerambycidae). Environ. Entomol. 38:1267–1275.

    Article  PubMed  CAS  Google Scholar 

  • Takakura, K. I. 2009. Reconsiderations on evaluating methodology of repellent effects: Validation of indices and statistical analyses. J. Econ. Entomol. 102:1977–1984.

    Article  PubMed  Google Scholar 

  • Terry, L. I. and Gardner, D. 1990. Male mating swarms in Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae). J. Insect Behav. 3:133–141.

    Article  Google Scholar 

  • Terry, I. and Schneider, M. 1993. Copulatory behaviour and mating frequency of the western flower thrips, Frankliniella occidentalis (Insecta: Thysanoptera). Zool. (J. Pure Appl. Zool.) 4:339–354.

    Google Scholar 

  • Webster, K. W., Cooper, P., and Mound, L. A. 2006. Studies on Kelly’s citrus thrips, Pezothrips kellyanus (Bagnall) (Thysanoptera: Thripidae): Sex attractants, host associations and country of origin. Aust. J. Entomol. 45:67–74.

    Article  Google Scholar 

  • Widemo, F. and Johansson, B. G. 2006. Male-male pheromone signalling in a lekking Drosophila. Proc. R. Soc. Lond. B Biol. Sci. 273:713–717.

    Article  CAS  Google Scholar 

  • Wright, S. P. 1992. Adjusted P-values for simultaneous inference. Biometrics 48:1005–1013.

    Article  Google Scholar 

  • Xiao, Y.-H., Zhang, J.-X., and Li, S.-Q. 2010. Male-specific (Z)-9-tricosene stimulates female mating behaviour in the spider Pholcus beijingensis. Proc. R. Soc. Lond. B Biol. Sci. 277:3009–3018.

    Article  CAS  Google Scholar 

  • Zhang, P.-J., Zhu, X.-Y., and Lu, Y.-B. 2011. Behavioural and chemical evidence of a male-produced aggregation pheromone in the flower thrips Frankliniella intonsa. Physiol. Entomol. 36:317–320.

    Article  CAS  Google Scholar 

  • Zhao, C.-Y., He, Y.-R., Zhong, F., Gao, Y., Qi, G.-J., Shao, X.-Y., and Lv, L.-H. 2011. Analysis of cuticular hydrocarbons of Frankliniella occidentalis. Chin. J. Appl. Entomol. 48:536–541.

    CAS  Google Scholar 

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Acknowledgments

Oladele Olaniran thanks the Education Trust Fund, Nigeria and Ladoke Akintola University of Technology, Ogbomoso, Nigeria for providing a training fellowship. Akella Sudhakar acknowledges the support of the European Union under a Marie Curie International Incoming Fellowship (Project No: 252258, Project Acronym: PERFECT). David Hall was funded by Defra Horticultural LINK Project HL 01107. We thank Dudley Farman (NRI) for preparing filter disks and running the GC/MS analyses of exposed disks.

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Correspondence to William D. J. Kirk.

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Olaniran, O.A., Sudhakar, A.V.S., Drijfhout, F.P. et al. A Male-Predominant Cuticular Hydrocarbon, 7-Methyltricosane, is used as a Contact Pheromone in the Western Flower Thrips Frankliniella occidentalis . J Chem Ecol 39, 559–568 (2013). https://doi.org/10.1007/s10886-013-0272-5

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