Abstract
The marriage of chemistry with ecology has been a productive one, providing a wealth of examples of how chemicals play important roles in the loves and lives of living organisms. At first the marriage may have been a simple and monogamous one with the major scientific aim of making proximate analyses of chemically mediated, individual level interactions. But times have changed and chemical ecology is broadening, embracing different approaches and disciplines. There is, for example, increasing appreciation of variability in the systems under study and an increase in evolutionary thinking. Another promising development is greater recognition of the potential importance of chemically mediated interactions for population dynamics and for structuring communities and species coexistence. The latter is an utterly underexplored area in chemical ecology. The field of chemical ecology of insect parasitoids shows some of these promising developments. Responses of parasitoids to infochemicals are increasingly studied with an integrated approach of mechanism and function. This integration of “how” and “why” questions significantly enhances the evolutionary and ecological understanding of stimulus–response patterns. The future challenge in chemical ecology is to demonstrate how chemically mediated interactions steer ecological and evolutionary processes at all levels of ecological organization. To reach this goal there is a need for interdisciplinary collaboration among chemists and ecologists working at different levels of organization and with different approaches, with other disciplines as partners.
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REFERENCES
Alborn, T., Turlings, T. C. J., Jones, T. H., Steinhagen, G., Loughrin, J. H., and Tumlinson, J. H. 1997. An elicitor of plant volatiles from beet armyworm oral secretion. Science 276:945–949.
Bell, W. J., Kipp, L. R., and Collins, R. D. 1995. The role of chemoorientation in search behavior, pp. 105–152, in R. T. Cardé and W. J. Bell (eds.). Chemical Ecology of Insects 2. Chapman & Hall, New York.
Berenbaum, M. R. 1995. The chemistry of defense: Theory and practice. Proc. Natl. Acad. Sci. U.S.A. 92:2–8.
Bernstein, C., Kacelnik, A., and Krebs, J. R. 1988. Individual decisions and the distribution of predators in a patchy environment. J. Anim. Ecol. 57:1007–1026.
Bernstein, C., Kacelnik, A., and Krebs, J. R. 1991. Individual decisions and the distribution of predators in a patchy environment. II. The influence of travel cost and structure of the environment. J. Anim. Ecol. 60:205–225.
CardÉ, R. T. and Bell, W. J. (eds.). 1995. Chemical Ecology of Insects 2. Chapman & Hall, New York.
Dicke, M. 1994. Local and systemic production of volatile herbivore-induced terpenoids: Their role in plant-carnivore mutualism. J. Plant Physiol. 143:465–472.
Dicke, M., and Vet, L. E. M. 1998. Plant-carnivore interactions: evolutionary and ecological consequences for plant, herbivore and carnivore, pp. 483–520 in H. Olff, V. K. Brown, and R. H. Drent (eds.). Herbivores between Plants and Predators. Blackwell Science, Oxford.
Dicke, M., Beek, T. A., van, Posthumus, M. A., Ben Dom, N., Bokhoven, H. van, and Groot, A. E. de. 1990. Isolation and identification of volatile kairomone that affects acarine predator-prey interactions. Involvement of host plant in its production. J. Chem. Ecol. 16:381–396.
Driessen, G., Bernstein, C., van Alphen, J. J. M., and Kacelnik, A. 1995. A count-down mechanism for host search in the parasitoid Venturia canescens. J. Anim. Ecol. 64:117–125.
Feeny, P. 1976. Plant apparency and chemical defense. Recent Adv. Phytochem. 10:1–40.
Futuyma, D. J. 1986. Evolutionary Biology, 2nd Ed. Sinauer Associates, Sunderland, Massachusetts.
Geervliet, J. B. F. 1997. Infochemical use by insect parasitoids in a tritrophic context: Comparison of a generalist and a specialist. PhD dissertation, Wageningen Agricultural University, Wageningen, The Netherlands.
Geervliet, J. B. F., Ariens, S., Dicke, M., and Vet, E. M. 1998. Long-distance assessment of patch profitability through volatile infochemicals by the parasitoids Cotesia glomerata and C. rubecula (Hymenoptera: Braconidae). Biol. Control 11:113–121.
Godfray, H. C. J. 1994. Parasitoids: Behavioral and Evolutionary Ecology. Princeton University Press, Princeton, New Jersey.
Haccou, P., Vlas, S. J. De, Van Alphen, J. J. M., and Visser, M. E. 1991. Information processing by foragers: Effects of intra-patch experience on the leaving tendency of Leptopilina heterotoma. J. Anim. Ecol. 60:93–106.
Hairston, N. G., Smith, F. E., and Slobodkin, L. B. 1960. Community structure, population control, and competition. Am. Nat. 94:421–425.
Hassell, M. P., and May, R. M. 1974. Aggregation of predators and insect parasites and its effect on stability. J. Anim. Ecol. 43:567–594.
Hedlund, K., Vet, L. E. M., and Dicke, M. 1996. Generalist and specialist parasitoid strategies of using odours of adult drosophilid flies when searching for larval hosts. Oikos 77:390–398.
Hemerik, L., Driessen, G., and Haccou, P. 1993. Effects of intra-patch experiences on patch time, search time and searching efficiency of the parasitoid Leptopilina clavipes (Hartig). J. Anim. Ecol. 62:33–44.
Jaenike, J. and Papaj, D. R. 1992. Behavioral plasticity and patterns of host use by insects, pp. 245–264, in B. D. Roitberg and M. B. Isman (eds.). Insect Chemical Ecology, An Evolutionary Approach. Chapman & Hall, New York.
Janssen, A., Van Alphen, J. J. M., Sabelis, M. W., and Bakker, K. 1995. Odour-mediated avoidance of competition in Drosophila parasitoids: the ghost of competition. Oikos 73:356–366.
Janssen, A., Pallini, A., Venzon, M., and Sabelis, M. W. 1998. Behaviour and indirect food web interactions among plant inhabiting arthropods. Exp. Appl. Acarol. In press.
Jones, C. G. 1988. What is chemical ecology?. J. Chem. Ecol. 14:727–730.
Karban, R., and Baldwin, I. T. 1997. Induced Responses to Herbivory. Chicago University Press, Chicago.
Lewis, W. J., Jones, R. L., Gross, H. R., and Nordlund, D. A. 1976. The role of kairomones and other behavioral chemicals in host finding by parasitic insects. Behav. Biol. 16:267–289.
LÖfstedt, C. 1990. Population variation and genetic control of pheromone communication systems in moths. Entomol. Exp. Appl. 54:199–218.
LÖfstedt, C. 1993. Moth pheromone genetics and evolution. Philos. Trans. R. Soc. B 340:167–177.
Lucas, E., Coderre, D., and Brodeur, J. 1998. Intraguild predation among aphid predators: Characterization and influence of extraguild prey density. Ecology, 79:1084–1092.
Mattiacci, L., Dicke, M., and Posthumus, M. A. 1995. Beta-glucosidase: An elicitor of herbivore-induced plant odor that attracts host-searching parasitic wasps. Proc. Natl. Acad. Sci. U.S.A. 92:2036–2040.
McNeil, J. N. 1991. Behavioral ecology of Pheromone-mediated communication in moths and its importance in the use of pheromone traps. Annu. Rev. Entomol. 36:407–430.
McNeil, J. N. 1992. Evolutionary perspectives and insect pest control: An attractive blend for the deployment of semiochemicals in management programmes, pp. 334–351, in B. D. Roitberg and M. B. Isman (eds.). Insect Chemical Ecology: An Evolutionary Approach. Chapman & Hall, New York.
McNeil, J. N., Delisle, J., and Cusson, M. 1997. Regulation of pheromone production in Lepidoptera: The need for an ecological perspective, pp. 31–41, in R. T. Cardé and A. K. Minks (eds.). Insect Pheromone Research: New Directions. Chapman & Hall, New York.
Murdoch, W. W., and Stewart-Oaten, A. 1989. Aggregation by parasitoids and predators: Effects on equilibrium and stability. Am. Nat. 134:288–310.
Nicholson, A. J. 1933. The balance of animal populations. J. Anim. Ecol. 2:132–178.
Pallini, A., Janssen, A., and Sabelis, M. W. 1997. Odour-mediated responses of phytophagous mites to conspecific and heterospecific competitors. Oecologia 100:179–185.
Papaj, D. R. 1993a. Automatic behavior and the evolution of instinct: Lessons from learning in parasitoids, pp. 243–272, in D. R. Papaj and A. C. Lewis (eds.). Insect Learning: Ecological and Evolutionary Aspects. Chapman & Hall, New York.
Papaj, D. R., 1993b. Afterword: Learning, adaptation and the lessons of O, pp. 374–386, in D. R. Papaj and A. C. Lewis (eds.). Insect Learning: Ecological and Evolutionary Aspects. Chapman & Hall, New York.
Papaj, R. D., and Vet, L. E. M. 1990. Odor learning and foraging success in the parasitoid, Leptopilina heterotoma. J. Chem. Ecol. 16:3137–3150.
Papaj, D. R., Snellen, H., Swaans, K., and Vet, L. E. M. 1994. Unrewarding experiences and their effect on foraging in the parasitic wasp Leptopilina heterotoma (Hymenoptera: Eucoilidae). J. Insect Behav. 7:465–481.
Phelan, P. L. 1997. Genetic and phylogenetics in the evolution of sex pheromones, pp. 563–579, in R. T. Cardé and A. K. Minks (eds.). Insect Pheromone Research: New Directions. Chapman & Hall, New York.
Polis, G. A., and Holt, R. D. 1992. Intraguild predation: the dynamics of complex trophic interactions. TREE 7:151–154.
Polis, G. A., and Strong, D. R. 1996. Food web complexity and community dynamics. Am. Nat. 147:814–846.
Price, P. W. 1991. Evolutionary theory of host and parasitoid interactions. Biol. Control. 1:83–93.
Price, P. W., Bouton, C. E., Gross, P., McPheron, B. A., Thompson, J. N., and Weis, A. E., 1980. Interactions among three trophic levels: Influence of plant on interactions between insect herbivores and natural enemies. Annu. Rev. Ecol. Syst. 11:41–65.
Rausher, M. D. 1992. Natural selection and the evolution of plant-insect interactions, pp. 20–88, in B. D. Roitberg and M. B. Isman (eds.). Insect Chemical Ecology: An evolutionary approach. Chapman & Hall, New York.
Roitberg, B. D. 1992. Why an evolutionary perspective? pp. 5–19, in B. D. Roitberg and M. B. Isman (eds.). Insect Chemical Ecology: An Evolutionary Approach. Chapman & Hall, New York.
Roitberg, B. D., and Isman, M. B. (eds.). 1992. Insect Chemical Ecology: An Evolutionary Approach. Chapman & Hall, New York.
Roitberg, B. D., and Mangel, M. 1988. On the evolutionary ecology of marking pheromones. Evol. Ecol. 2:289–315.
Rosenheim, J. A., Wilhoit, L. R., and Armer, C. A. 1993. Influence of intraguild predation among generalist insect predators on the suppression of an herbivore population. Oecologia 96:439–449.
Schoonhoven, L. M., Jermy, T. and Van Loon, J. J. A. 1998. Insect-Plant Biology: From Physiology to Evolution. Chapman & Hall, London.
Silverstein, R. M. 1990. Practical use of pheromones and other behavior-modifying compounds: Overview, pp. 1–8, in R. L. Ridgway, R. M. Silverstein, and M. N. Inscoe (eds.). Behavior-Modifying Chemicals for Insect Management: Applications of Pheromones and Other Attractants. Marcel Dekker, New York.
Stephens, D. W., and Krebs, J. R. 1986. Foraging Theory. Princeton University Press, Princeton, New Jersey.
Taylor, A. D. 1993. Heterogeneity in host-parasitoid interactions: “Aggregation of risk” and the “CV2 > 1 rule.” TREE 8:400–405.
Tinbergen, N. 1963. On the aims and methods of ethology. Z. Tierpsychol. 20:410–433.
Tumlinson, J. H., Turlings, T. C. J., and Lewis, W. J. 1993. Semiochemically mediated foraging behavior in beneficial parasitic insects. Arch. Insect Biochem. Physiol. 22:385–391.
Turlings, T. C. J., Tumlinson, J. H., and Lewis, W. J. 1990. Exploitation of herbivore-induced plant odors by host-seeking parasitic wasps. Science 250:1251–1253.
Turlings, T. C. J., Wackers, F. L., Vet, L. E. M., Lewis, W. J., and Tumlinson, J. H. 1993. Learning of host-finding cues by hymenopterous parasitoids, pp. 51–78, in D. R. Papaj and A. C. Lewis (eds.). Insect Learning. Chapman & Hall, New York.
UchmÁnski, J., and Grimm, V. 1996. Individual-based modelling in ecology: What makes the difference? TREE 11:437–441.
van Alphen, J. J. M., and Visser, M. E. 1990. Superparasitism as an adaptive strategy for insect parasitoids. Annu. Rev. Entomol. 35:59–79.
Vet, L. E. M. 1996. Parasitoid foraging: The importance of variation in individual behaviour for population dynamics, pp. 245–256, in R. B. Floyd and A. W. Sheppard (eds.). Frontiers of Population Ecology, CSIRO Publishing, Melboume, Australia.
Vet, L. E. M., and van Alphen, J. J. M. 1985. A comparative functional approach to the host detection behaviour of parasitic wasps. I. A. qualitative study on Eucoilidae and Alysiinae. Oikos 44:478–486.
Vet, L. E. M., and Dicke, M. 1992. Ecology of infochemical use by natural enemies in a tritrophic context. Annu. Rev. Entomol. 37:141–172.
Vet, L. E. M., and Janse, C. J. 1984. Fitness of two sibling species of Asobara (Braconidae: Alysiinae), larval parasitoids of Drosophilidae in different microhabitats. Ecol. Entomol. 9:345–354.
Vet, L. E. M., and Papaj, D. R. 1992. Effects of experience on parasitoid movement in odour plumes. Physiol. Entomol. 17:90–96.
Vet, L. E. M., Lewis, W. J., Papaj, D. R., and Lenteren, J. C. van. 1990. A variable-response model for parasitoid foraging behavior. J. Insect Behav. 3:471–490.
Vet, L. E. M., WÄckers, F. L., and Dicke, M. 1991. How to hunt for hiding hosts: The reliability-detectability problem in foraging parasitoids. Neth. J. Zool. 41:202–213.
Vet, L. E. M., Lewis, W. J., and CardÉ, R. T. 1995. Parasitoid foraging and learning, pp. 65–101, in R. T. Cardé and W. J. Bell (eds.), Chemical Ecology of Insects 2. Chapman & Hall, New York.
Vet, L. E. M., De Jong, A. G., Franchi, E., and Papaj, D. R. 1998. The effect of complete versus incomplete information on odour discrimination in a parasitic wasp. Anim. Behav. 55:1271–1279.
Vinson, S. B., 1984. Parasitoid-host relationships, pp. 205–233, in W. J. Bell and R. T. Cardé (eds.). Chemical Ecology of Insects. Chapman and Hall, London.
Vos, M., Hemerik, L., and Vet, L. E. M. 1998. Patch exploitation by the parasitoids Cotesia glomerata and Cotesia rubecula in multi-patch environments with different host distributions. J. Anim. Ecol. 67:774–783.
Weisser, W. W., and Houston, A. I. 1993. Host discrimination in parasitic wasps: When is it advantageous? Funct. Ecol. 7:27–39.
Wiskerke, J. S. C., Dicke, M., and Vet, L. E. M. 1993. Larval parasitoid uses aggregation pheromone of adult hosts in foraging behaviour: A solution to the reliability-detectability problem. Oecologia 93:145–148.
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Vet, L.E.M. From Chemical to Population Ecology: Infochemical Use in an Evolutionary Context. J Chem Ecol 25, 31–49 (1999). https://doi.org/10.1023/A:1020833015559
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DOI: https://doi.org/10.1023/A:1020833015559