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Different uses of plant semiochemicals in host location strategies of the two tachinid parasitoids

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Abstract

Some members of the family Tachinidae (Insecta: Diptera) deposit numerous very small eggs, termed “microtype” eggs, on the food plants of their caterpillar hosts. Parasitization is successful only when the hosts ingest these eggs. To increase the chance of hosts encountering the eggs, microtype tachinid parasitoids have to choose a suitable plant that harbors hosts and lay their eggs near the hosts. In their host location process, semiochemicals emitted by host-infested plants offer the tachinids a reliable cue. We investigated the behavioral responses of two microtype tachinid parasitoids, Pales pavida and Zenillia dolosa, to maize plants infested with their caterpillar host, Mythimna separata, in a wind tunnel. P. pavida females showed a significantly higher rate of landing on caterpillar-infested plants than on mechanically wounded or intact plants, whereas Z. dolosa landed on both the caterpillar-infested and mechanically wounded plants at significantly higher rates than on intact plants. We also examined which part of a caterpillar-infested maize leaf induces oviposition. P. pavida deposited eggs on the margin of the leaf, whereas Z. dolosa preferentially laid eggs around a caterpillar-infested area or a mechanically wounded spot. P. pavida eggs retained their parasitization ability for more than 15 days after they were deposited, whereas the eggs of Z. dolosa could not survive more than 5 days after oviposition. Our results suggest that each tachinid parasitoid employs a different host location strategy to exploit semiochemicals coming from plant–herbivore interaction as cues in order to increase their parasitization success.

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References

  • Belshaw R (1994) Life history characteristics of Tachinidae (Diptera) and their effect on polyphagy. In: Hawkins BA, Sheehan W (eds) Parasitoid community ecology. Oxford University Press, New York, pp 145–162

    Google Scholar 

  • Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J Roy Statist Soc Ser B 57:289–300

    Google Scholar 

  • Chamberlain K, Khan ZR, Pickett JA, Toshova T, Wadhams LJ (2006) Diel periodicity in the production of green leaf volatiles by wild and cultivated host plants of stemborer moths, Chilo partellus and Busseola fusca. J Chem Ecol 32:565–577

    Article  PubMed  CAS  Google Scholar 

  • Clement SL, Rubink WL, McCartney DA (1986) Larviposition response of Bonnetia comta (Dipt.: Tachinidae) to a kairomone of Agrotis ipsilon (Lep.: Noctuidae). Entomophaga 31:277–284

    Article  Google Scholar 

  • De Moraes CM, Lewis WJ, Paré PW, Alborn HT, Tumlinson JH (1998) Herbivore-infested plants selectively attract parasitoids. Nature 393:570–573

    Article  Google Scholar 

  • Dicke M (2009) Behavioural and community ecology of plants that cry for help. Plant Cell Environ 32:654–665

    Article  PubMed  CAS  Google Scholar 

  • Dicke M, Baldwin IT (2010) The evolutionary context for herbivore-induced plant volatiles: beyond the ‘cry for help’. Trends Plant Sci 15:167–175

    Article  PubMed  CAS  Google Scholar 

  • Feener DH Jr, Brown BV (1997) Diptera as parasitoids. Annu Rev Entomol 42:73–97

    Article  PubMed  CAS  Google Scholar 

  • Fukushima J, Kainoh Y, Honda H, Takabayashi J (2002) Learning of herbivore-induced and nonspecific plant volatiles by a parasitoid, Cotesia kariyai. J Chem Ecol 28:579–586

    Article  PubMed  CAS  Google Scholar 

  • Hanyu K, Ichiki RT, Nakamura S, Kainoh Y (2009) Duration and location of attraction to herbivore-damaged plants in the tachinid parasitoid Exorista japonica. Appl Entomol Zool 44:371–378

    Article  Google Scholar 

  • Hanyu K, Ichiki RT, Nakamura S, Kainoh Y (2011) Behavior of the tachinid parasitoid Exorista japonica (Diptera: Tachinidae) on herbivore-infested plants. Appl Entomol Zool 46:565–571

    Article  Google Scholar 

  • Hassell MP (1968) The behavioural response of a tachinid fly (Cyzenis albicans (Fall.)) to its host, the winter moth (Operophtera brumata (L.)). J Anim Ecol 37:627–639

    Article  Google Scholar 

  • Hattori M, Atsusawa S (1980) Mass-rearing of the cabbage armyworm, Mamestra brassicae Linné, and the common armyworm, Mythimna separata Walker (Lepidoptera: Noctuidae), on a simple artificial diet. Jpn J Appl Entomol Zool 24:36–38 (in Japanese with English summary)

    Article  Google Scholar 

  • Herting B, Dely-Draskovits A (1993) Family Tachinidae. In: Soós Á, Papp L (eds) Catalogue of Palaearctic Diptera, vol 13, Anthomyiidae–Tachinidae. Hungarian Natural History Museum, Budapest, pp 118–458

    Google Scholar 

  • Hirai N, Ishii M (2002) Egg placement of the tachinid fly Sturmia bella on leaves of the evergreen milkvine Marsdenia tomentosa and the feeding habit of its host butterfly Parantica sita. Entomol Sci 5:153–159

    Google Scholar 

  • Ho GTT, Ichiki RT, Nakamura S (2011) Reproductive biology of the microtype tachinid fly Zenillia dolosa (Meigen) (Diptera: Tachinidae). Entomol Sci 14:210–215

    Article  Google Scholar 

  • Hoballah MEF, Tamo C, Turlings TCJ (2002) Differential attractiveness of induced odors emitted by eight maize varieties for the parasitoid Cotesia marginiventris: Is quality of quantity important? J Chem Ecol 28:951–962

    Article  PubMed  CAS  Google Scholar 

  • Huang P (1981) Laboratory rearing of Pales pavida (Dip: Tachinidae) on substitute host Galleria mellonella (Lep: Galleriidae). Z Pflanzenk Pflanzen 88:177–188 (in German with English summary)

    Google Scholar 

  • Ichiki RT, Kainoh Y, Kugimiya S, Takabayashi J, Nakamura S (2008) Attraction to herbivore-induced plant volatiles by the host-foraging parasitoid fly Exorista japonica. J Chem Ecol 34:614–621

    Article  PubMed  CAS  Google Scholar 

  • Ichiki RT, Kainoh Y, Yamawaki Y, Nakamura S (2011) The parasitoid fly Exorista japonica uses visual and olfactory cues to locate herbivore-infested plants. Entomol Exp Appl 138:175–183

    Article  Google Scholar 

  • Kainoh Y, Tanaka C, Nakamura S (1999) Odor from herbivore-damaged plant attracts a parasitoid fly, Exorista japonica Townsend (Diptera: Tachinidae). Appl Entomol Zool 34:463–467

    Google Scholar 

  • Mondor EB, Roland J (1997) Host locating behaviour of Leschenaultia exul and Patelloa pachypyga: two tachinid parasitoids of the forest tent caterpillar, Malacosoma disstria. Entomol Exp Appl 85:161–168

    Article  Google Scholar 

  • Monteith LG (1955) Host preferences of Drino bohemica Mesn. (Diptera: Tachinidae), with particular reference to olfactory responses. Can Entomol 87:509–530

    Article  Google Scholar 

  • Monteith LG (1964) Influence of the health of the food plant of the host on host-finding by tachinid parasites. Can Entomol 96:1477–1482

    Article  Google Scholar 

  • Odell TM, Godwin PA (1984) Host selection by Blepharipa pratensis (Meigen), a tachinid parasite of the gypsy moth, Lymantria dispar L. J Chem Ecol 10:311–320

    Article  Google Scholar 

  • Potting RPJ, Vet LEM, Dicke M (1995) Host microhabitat location by stem-borer parasitoid Cotesia flavipes: the role of herbivore volatiles and locally and systemically induced plant volatiles. J Chem Ecol 21:525–539

    Article  CAS  Google Scholar 

  • R Development Core Team (2008) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. Available via http://www.R-project.org

  • Roland J (1986) Parasitism of winter moth in British Columbia during build-up of its parasitoid Cyzenis albicans: attack rate on oak v. apple. J Anim Ecol 55:215–234

    Article  Google Scholar 

  • Roland J, Evans WG, Myers JH (1989) Manipulation of oviposition patterns of the parasitoid Cyzenis albicans (Tachinidae) in the field using plant extracts. J Insect Behav 2:487–503

    Article  Google Scholar 

  • Roland J, Denford KE, Jimenez L (1995) Borneol as an attractant for Cyzenis albicans, a tachinid parasitoid of the winter moth, Operophtera brumata L. (Lepidoptera, Geometridae). Can Entomol 127:413–421

    Article  Google Scholar 

  • Roth JP, King EG, Hensley SD (1982) Plant, host, and parasite interactions in the host selection sequence of the tachinid Lixophaga diatraeae. Environ Entomol 11:273–277

    Google Scholar 

  • Shima H (2006) A host–parasite catalog of Tachinidae (Diptera) of Japan. Makunagi/Acta Dipt 31:1–171

    Google Scholar 

  • Shiojiri K, Ozawa R, Matsui K, Kishimoto K, Kugimiya S, Takabayashi J (2006) Role of the lipoxygenase/lyase pathway of host–food plants in the host searching behavior of two parasitoid species, Cotesia glomerata and Cotesia plutellae. J Chem Ecol 32:969–979

    Article  PubMed  CAS  Google Scholar 

  • Stireman JO III, O’Hara JE, Wood DM (2006) Tachinidae: evolution, behavior, and ecology. Annu Rev Entomol 51:525–555

    Article  PubMed  CAS  Google Scholar 

  • Tachi T, Shima H (2010) Molecular phylogeny of the subfamily Exoristinae (Diptera, Tachinidae), with discussions on the evolutionary history of female oviposition strategy. Syst Entomol 35:148–163

    Article  Google Scholar 

  • Takabayashi J, Noda T, Takahashi S (1991) Plants produce attractants for Apanteles kariyai, a parasitoid of Pseudaletia separata; cases of ‘communication’ and ‘misunderstanding’ in parasitoid–plant interactions. Appl Entomol Zool 26:237–243

    Google Scholar 

  • Takabayashi J, Takahashi S, Dicke M, Posthumus MA (1995) Developmental stage of the herbivore Pseudaletia separata affects production of herbivore-induced synomone by maize plants. J Chem Ecol 21:273–287

    Article  CAS  Google Scholar 

  • Tanaka C, Kainoh T, Honda H (2001) Host frass as arrestant chemicals in locating host Mythimna separata by the tachinid fly Exorista japonica. Entomol Exp Appl 100:173–178

    Article  Google Scholar 

  • Thompson AC, Roth JP, King EG (1983) Larviposition kairomone of the tachinid Lixophaga diatraeae. Environ Entomol 12:1312–1314

    CAS  Google Scholar 

  • Turlings TCJ, Tumlinson JH (1992) Systemic release of chemical signals by herbivore-injured maize. Proc Natl Acad Sci USA 89:8399–8402

    Article  PubMed  CAS  Google Scholar 

  • Turlings TCJ, Wäckers FL (2004) Recruitment of predators and parasitoids by herbivore-injured plants. In: Cardé RT, Millar JG (eds) Advances in insect chemical ecology. Cambridge University Press, Cambridge, pp 21–75

    Chapter  Google Scholar 

  • Turlings TCJ, Tumlinson JH, Lewis WJ (1990) Exploitation of herbivore-induced plant odors by host-seeking parasitic wasps. Science 250:1251–1253

    Article  PubMed  CAS  Google Scholar 

  • Turlings TCJ, Lengwiler UB, Bernasconi ML, Wechsler D (1998) Timing of induced volatile emissions in maize seedlings. Planta 207:146–152

    Article  CAS  Google Scholar 

  • Vet LEM, Dicke M (1992) Ecology of infochemical use by natural enemies in a tritrophic context. Annu Rev Entomol 37:141–172

    Article  Google Scholar 

  • Wickremasinghe MGV, van Emden HF (1992) Reactions of adult female parasitoids, particularly Aphidius rhopalosiphi, to volatile chemical cues from the host plants of their aphid prey. Physiol Entomol 17:297–304

    Article  CAS  Google Scholar 

Download references

Acknowledgments

We are grateful to Drs. Hiroshi Shima and Takuji Tachi of Kyushu University for their useful comments on the manuscript and for providing insect materials. We also thank Aki Konishi, Yuriko Akagi, Yukie Muraki, and Chieko Yokokura of the Japan International Research Center for Agricultural Sciences for technical assistance. This work was supported by a Research Fellowship (to Ryoko T. Ichiki) through the Japan Society for the Promotion of Science.

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Correspondence to Ryoko T. Ichiki.

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Communicated by: Sven Thatje

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Ichiki, R.T., Ho, G.T.T., Wajnberg, E. et al. Different uses of plant semiochemicals in host location strategies of the two tachinid parasitoids. Naturwissenschaften 99, 687–694 (2012). https://doi.org/10.1007/s00114-012-0950-0

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