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Treating hop plants with (Z)-jasmone increases colonization by Phorodon humuli (Hemiptera: Aphididae) spring migrants

Published online by Cambridge University Press:  24 May 2007

T.W. Pope*
Affiliation:
East Malling Research, New Road, East Malling, Kent, ME19 6BJ, UK Imperial College London, Faculty of Natural Sciences, Division of Biology, Silwood Park Campus, Ascot, Berkshire, SL5 7PY, UK
C.A.M. Campbell
Affiliation:
East Malling Research, New Road, East Malling, Kent, ME19 6BJ, UK
J. Hardie
Affiliation:
Imperial College London, Faculty of Natural Sciences, Division of Biology, Silwood Park Campus, Ascot, Berkshire, SL5 7PY, UK
L.J. Wadhams
Affiliation:
Rothamsted Research, Harpenden, Hertfordshire, AL5 2JQ, UK
*
*Address for correspondence: Imperial College London, Faculty of Natural Sciences, Division of Biology, Wye Campus, Ashford, Kent, TN25 5AH, UK Fax: +44 (0)20 7594 2669 E-mail: t.pope@imperial.ac.uk

Abstract

Hop plants were sprayed with (Z)-jasmone, at a rate of 50 g ha−1, during the spring migration of the damson–hop aphid Phorodon humuli (Schrank) in 2002 and 2003. Numbers of P. humuli spring migrants colonizing hop plants, Humulus lupulus L., 2–6 and 7–11 days after applying this treatment were assessed in both years. During the first five-day period, significantly more spring migrants were found on hop plants treated with (Z)-jasmone, in comparison with control plants, in 2002. By contrast, no significant difference was evident in the second five-day period. Although the migration in 2003 was much lighter than in 2002, greater numbers of migrants were again removed from treated plants. Indeed, more spring migrants were removed from plants sprayed with (Z)-jasmone in this year during both five-day periods (11 and 44%, respectively) compared with the 23% greater numbers removed in the first five-day period in 2002. Therefore, unlike some other species of aphid, where numbers were consistently lower on plots sprayed with (Z)-jasmone, spraying the secondary host of P. humuli with this compound appears to increase colonization by spring migrants.

Type
Short Communication
Copyright
Copyright © Cambridge University Press 2007

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References

Barber, A., Campbell, C.A.M., Crane, H., Darby, P. & Lilley, R. (2003) Cost-benefits of reduced aphicide usage on dwarf hops susceptible and partially resistant to damson–hop aphid. Annals of Applied Biology 143, 3544.Google Scholar
Birkett, M.A., Campbell, C.A.M., Chamberlain, K., Guerrieri, E., Hick, A.J., Martin, J.L., Matthes, M., Napier, J.A., Pickett, J.A., Poppy, G.M., Pow, E.M., Pye, B.J., Smart, L.E., Wadhams, G.H., Wadhams, L.J. & Woodcock, C.M. (2000) New roles for cis-jasmone as an insect semiochemical and in plant defense. Proceedings of the National Academy of Sciences, USA 97, 93299334.CrossRefGoogle ScholarPubMed
Blechert, S., Brodschelm, W., Hölder, S., Kammerer, L., Kutchan, T.M., Mueller, M.J., Xia, Z.-Q. & Zenk, M.H. (1995) The octadecanoic pathway: signal molecules for the regulation of secondary pathways. Proceedings of the National Academy of Sciences, USA 92, 40994105.CrossRefGoogle ScholarPubMed
Bruce, T.J.A., Martin, J.L., Pickett, J.A., Pye, B.J., Smart, L.E. & Wadhams, L.J. (2003) cis-Jasmone treatment induces resistance in wheat plants against the grain aphid, Sitobion avenae (Fabricius) (Homoptera: Aphididae). Pest Management Science 59, 10311036.CrossRefGoogle Scholar
Chamberlain, K., Guerrieri, E., Pennacchio, F., Pettersson, J., Pickett, J.A., Poppy, G.M., Powell, W., Wadhams, L.J. & Woodcock, C.M. (2001) Can aphid-induced plant signals be transmitted aerially and through the rhizosphere? Biochemical Systematics and Ecology 29, 10631074.CrossRefGoogle Scholar
Farmer, E.E. & Ryan, C.A. (1990) Interplant communication: airborne methyl jasmonate induces synthesis of protinase inhibitors in plant leaves. Proceedings of the National Academy of Sciences, USA 87, 77137716.CrossRefGoogle Scholar
Koch, T., Bandemer, K. & Boland, W. (1997) Biosynthesis of cis-jasmone: a pathway for the inactivation and the disposal of the plant stress hormone jasmonic acid to the gas phase. Helvetica Chimica Acta 80, 838850.CrossRefGoogle Scholar
Loughrin, J.H., Manukian, A., Heath, R.R. & Tumlinson, J.H. (1995) Volatiles emitted by different cotton varieties damaged by feeding beet armyworm larvae. Journal of Chemical Ecology 21, 12171227.CrossRefGoogle ScholarPubMed
Paré, P.W. & Tumlinson, J.H. (1997) De novo biosynethesis of volatiles induced by insect herbivory in cotton plants. Plant Physiology 114, 11611167.CrossRefGoogle Scholar
Payne, R.W. (2000) The guide to GenStat. Part 2: statistics. Oxford, VSN International.Google Scholar
Pickett, J.A., Rasmussen, H.B., Woodcock, C.M., Matthes, M. & Napier, J.A. (2003) Plant stress signalling: understanding and exploiting plant–plant interactions. Biochemical Society Transactions 31, 123127.CrossRefGoogle ScholarPubMed
Turlings, T.C.J., Loughrin, J.H., McCall, P.J., Röse, U.S.R., Lewis, W.J. & Tumlinson, J.H. (1995) How caterpillar-damaged plants protect themselves by attracting parasitic wasps. Proceedings of the National Academy of Sciences, USA 92, 41694174.CrossRefGoogle ScholarPubMed
Way, M.J. & Cammell, M.E. (1970) Self regulation in aphid populations. pp. 232242in den Boer, P.J. & Gradwell, G.R. (Eds) Proceedings of the Adanced Study Institute on ‘Dynamics of numbers in populations’ Oosterbeek, The Netherlands, 7–18 September 1970. Wageningen, The Netherlands,Centre for Agricultural Publishing and Documentation.Google Scholar