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Induction of Volatile Emissions in Maize by Different Larval Instars of Spodoptera littoralis

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Abstract

Maize plants under attack by caterpillars emit a specific blend of volatiles that is highly attractive to parasitic wasps. The release of these signals is induced by elicitors in the caterpillar regurgitant. Studies suggest that plants respond differently to different herbivore species and even to different herbivore stages, thus providing parasitoids and predators with specific signals. We tested if this is the case for different larval instars of the noctuid moth Spodoptera littoralis when they feed on maize plants. Cut maize plants were incubated in diluted regurgitant from second, third, or fifth instar caterpillars. There were no differences in total amount released after these treatments, but there were small differences in the release of the minor compounds phenethyl acetate and α-humulene. Regurgitant of all three instars contained the elicitor volicitin. To test the effect of actual feeding by the larvae, potted plants were infested with caterpillars of one of the three instars, and volatiles were collected the following day. The intensity of the emissions was correlated with the number of larvae feeding on a plant, and with the amount of damage inflicted, but was independent of the instar that caused the damage. We also used artificial damage to mimic the manner of feeding of each instar to test the importance of physical aspects of damages for the odor emission. The emission was highly variable, but no differences were found among the different types of damage. In olfactometer tests, Microplitis rufiventris, a parasitoid that can only successfully parasitize second and early third instar S. littoralis, did not differentiate among the odors of maize plants attacked by different instar larvae. The odor analyses as well as the parasitoid's responses indicate that maize odors induced by S. littoralis provide parasitoids with poor information on the larval developmental stage. We discuss the results in the context of variability and lack of specificity in odorous plant signals.

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References

  • Agelopoulos, N. G. and Keller, M. A. 1994. Plant-natural enemy association in tritrophic system, Cotesia rubecula-Pieris rapae-Brassicaceae (Cruciferae) III: Collection and identification of plant and frass volatiles. J. Chem. Ecol. 20:1955-1967.

    Google Scholar 

  • Alborn, H. T., Turlings, T. C. J., Jones, T. H., Stenhagen, G., Loughrin, J. H., and Tumlinson, J. H. 1997. An elicitor of plant volatiles from beet armyworm oral secretion. Science 276:945-949.

    Google Scholar 

  • Alborn, H. T., Jones, T. H., Stenhagen, G. S., and Tumlinson, J. H. 2000. Identification and synthesis of volicitin and related components from beet armyworm oral secretions. J. Chem. Ecol. 26:203-220.

    Google Scholar 

  • De Moraes, C. M., Lewis, W. J., Paré, P. W., Alborn, H. T., and Tumlinson, J. H. 1998. Herbivore-infested plants selectively attract parasitoids. Nature 393:570-573.

    Google Scholar 

  • Dicke, M. and Sabelis, M. W. 1988. How plants obtain predatory mites as bodyguards. Neth. J. Zool. 38:148-165.

    Google Scholar 

  • Dicke, M., Sabelis, M. W., Takabayashi, J., Bruin, J., and Posthumus, M. A. 1990. Plant strategies of manipulating predator-prey interactions through allelochemicals: prospects for application in pest control. J. Chem. Ecol. 16:3091-3118.

    Google Scholar 

  • Dicke, M., van Baarlen, P., Wessels, R., and Dikman, H. 1993. Herbivory induces systemic production of plant volatiles that attract predators of the herbivore: extraction of endogenous elicitor. J. Chem. Ecol. 19:581-599.

    Google Scholar 

  • Du, Y., Poppy, G. M., Powell, W., Pickett, J. A., Wadhams, L. J., and Woodcock, C. M. 1998. Identification of semiochemicals released during aphid feeding that attract parasitoid Aphidius ervi. J. Chem. Ecol. 24:1355-1368.

    Google Scholar 

  • Gouinguené, S. P. and Turlings, T. C. J. 2002, The effects of abiotic factors on induced emissions in corn plant. Plant Physiol. 129:1296-1307.

    Google Scholar 

  • Gouinguené, S., Degen, T., and Turlings, T. C. J. 2001. Variability in herbivore-induced odour emissions among maize cultivars and their wild ancestors (teosinte). Chemoecology 11:9-16.

    Google Scholar 

  • Guerrieri, E., Poppy, G. M., Powell, W., Tremblay, E., and Pennachio, F. 1999. Induction and systemic release of herbivore-induced plant volatiles mediating in-flight orientation of Aphidius ervi. J. Chem. Ecol. 25:1247-1261.

    Google Scholar 

  • Heath, B. and Manukian, A. 1994. An automated system for use in collecting volatile chemicals released from plants. J. Chem. Ecol. 20:593-608.

    Google Scholar 

  • Lewis, W. J. and Tumlinson, J. H. 1988. Host detection by chemically mediated associative learning in a parasitic wasp. Nature 331:257-259.

    Google Scholar 

  • Loke, W. H. and AshleyT. R. 1984. Sources of fall armyworm, Spodotera frugiperda (Lepidoptera:Noctuidae), kairomones eliciting host-finding behavior in Cotesia (=Apantales) marginiventris (Hymenoptera:Braconidae). J. Chem. Ecol. 10:1019-1027.

    Google Scholar 

  • Mattiacci, L. and DickeM. 1995. Host-age discrimination during host location by Cotesia glomerata, a larval parasitoid of Pieris brassicae. Entomol. Exp. Appl. 76:37-48.

    Google Scholar 

  • Mattiacci, L., Dicke, M., and Posthumus, M. A. 1994. Induction of parasitoid attracting synomone in brussel sprouts plants by feeding of Pieris brassicae larvae: role of mechanical damage and herbivore elicitor. J. Chem. Ecol. 20:2229-2247.

    Google Scholar 

  • McCall, P. J., Turlings, T. C. J., Lewis, W. J., and Tumlinson, J. H. 1993. Role of plant volatiles in host location by the specialist parasitoid Microplitis croceipes Cresson (Braconidae: Hymenoptera). J. Insect Behav. 6:625-639.

    Google Scholar 

  • Mori, N., Alborn, H. T., TealP. E. A., and TumlinsonJ. H. 2001. Enzymatic decomposition of elicitors of plant volatiles in Heliothis virescens and Helicorpa zea. J. Insect Physiol. 47:749-757.

    Google Scholar 

  • Röse, U. S. R., Manukian, A., Heath, R. R., and TumlinsonJ. H. 1996. Volatile semiochemicals released from undamaged cotton leaves. A systemic response of living plants to caterpillar damage. Plant Physiol. 111:487-495.

    Google Scholar 

  • Steinberg, S., Dicke, M., Vet, L. E. M., and WanningenR. 1992. Response to the braconid parasitoid Cotesia (=Apanteles) glomerata to volatile infochemicals: Effects of bioassay set-up, parasitoid age and experience and barometric flux. Entomol. Exp. Appl. 63:163-175.

    Google Scholar 

  • Takabayashi, J., Takahashi, S., Dicke, M., and Posthumus, M. A. 1995. Developmental stage of herbivore Pseudaletia separata affects production of herbivore-induced synomone by corn plants. J. Chem. Ecol. 21:273-287.

    Google Scholar 

  • Turlings, T. C. J., Alborn, H. T., Loughrin, J. H., and Tumlinson, J. H. 2000. Volicitin, an elicitor of maize volatiles in oral secretion of Spodopters exigua: Isolation and bioactivity. J. Chem. Ecol. 26:189-202.

    Google Scholar 

  • TurlingsT. C. J., Lengwiler, U. B., Bernasconi, M. L., and Wechsler, D. 1998. Timing of induced volatile emissions in maize seedlings. Planta 207:146-152.

    Google Scholar 

  • Turlings, T. C. J., McCall, P. J., AlbornH. T., and Tumlinson, J. H. 1993a. An elicitor in caterpillar oral secretions that induces corn seedlings to emit chemical signals attractive to parasitic wasps. J. Chem. Ecol. 19:411-425.

    Google Scholar 

  • Turlings, T. J. C., TumlinsonJ. H., and Lewis, W. J. 1990. Exploitation of herbivore-induced plant odors by host-seeking parasitic wasps. Science 250:1251-1253.

    Google Scholar 

  • Turlings, T. C. J., Wäckers, F., Vet, L. E. M., Lewis, J., and Tumlinson, J. H. 1993b. Learning of host-finding cues by Hymenopterous parasitoids. pp. 51-78, in D. R. Papaj, A. C. Lewis (Eds.), Insect Learning, Ecological and Evolutionary Persperctives, Chapman & Hall, New York.

    Google Scholar 

  • Turlings, T. J. C., Tumlinson, J. H., Heath, R. R., Proveaux, A. T., and Doolittle, R. E. 1991. Isolation and identification of allelochemicals that attract the larval parasitoid, Cotesia marginiventris (CRESSON), to the microhabitat of one its host. J. Chem. Ecol. 17:2235-2251.

    Google Scholar 

  • Vet, L. E. M., and Dicke, M. 1992. Ecology of infochemicals use by natural enemies in a tritrophic context. Annu. Rev. Entomol. 37:141-172.

    Google Scholar 

  • VetL. E. M., Lewis, W. J., and Cardé, R. T. 1995. Parasitoid foraging and learning pp. 65-100, in R. T. Cardé, and W. J. Bell (eds), Chemical Ecology of Insects 2, Chapman & Hall, Sterling, Virginia.

    Google Scholar 

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Correspondence to Ted C. J. Turlings.

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Gouinguené, S., Alborn, H. & Turlings, T.C.J. Induction of Volatile Emissions in Maize by Different Larval Instars of Spodoptera littoralis . J Chem Ecol 29, 145–162 (2003). https://doi.org/10.1023/A:1021984715420

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