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Chapter 6 - Population dynamics and species interactions

Published online by Cambridge University Press:  01 September 2010

Edward B. Radcliffe
Affiliation:
University of Minnesota
William D. Hutchison
Affiliation:
University of Minnesota
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Summary

Agricultural monocultures are often thought to be more prone to herbivore outbreaks than natural systems, and early agroecologists posited that the lack of biodiversity in agricultural systems contributes to their instability (Pimentel, 1961; van Emden & Williams, 1974). In contrast, some detailed reviews have concluded that perhaps one or two particularly effective natural enemies are all that is needed for effective pest control (Hawkins et al., 1999). Such issues come to the fore when a decision must be made in classical biological control about whether to introduce one or several natural enemy species in an effort to control exotic pests (Myers et al., 1989; Denoth et al., 2002), and when designing schemes to conserve indigenous natural enemies by modifying cultural practices (Landis et al., 2000; Tscharntke et al., 2005). Here, we first review the major classes of natural enemies – specialists and generalists – and the traits of each that are likely to contribute to (or detract from) their effectiveness as biological control agents. We then discuss interactions within diverse communities of natural enemies that are likely to affect biological control.

Specialist natural enemies: the best biological control agents?

Biological control practitioners have long debated the question: what are the traits of an effective biological control agent? General consensus seems to focus around a few traits that a successful agent will possess (see Chapter 9).

Type
Chapter
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Integrated Pest Management
Concepts, Tactics, Strategies and Case Studies
, pp. 62 - 74
Publisher: Cambridge University Press
Print publication year: 2008

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References

Bengtsson, J., Ahnström, J. & Weibull, A. (2005). The effects of organic agriculture on biodiversity and abundance: a meta-analysis. Journal of Applied Ecology, 42, 261–269.CrossRefGoogle Scholar
Briggs, C. J. & Hoopes, M. F. (2004). Stabilizing effects in spatial parasitoid–host and predator–prey models: a review. Theoretical Population Biology, 65, 299– 315.CrossRefGoogle ScholarPubMed
Cardinale, B. J., Harvey, C. T., Gross, K. & Ives, A. R. (2003). Biodiversity and biocontrol: emergent impacts of a multi-enemy assemblage on pest suppression and crop yield in an agroecosystem. Ecology Letters, 6, 857–865.CrossRefGoogle Scholar
Cardinale, B. J., Srivastava, D., Duffy, J. E.et al. (2006). Effects of biodiversity on the functioning of trophic groups and ecosystems. Nature, 443, 989–992.CrossRefGoogle ScholarPubMed
Casula, P., Wilby, A. & Thomas, M. B. (2006). Understanding biodiversity effects on prey in multi-enemy systems. Ecology Letters, 9, 995–1004.CrossRefGoogle ScholarPubMed
Debach, P. & Rosen, D. (1991). Biological Control by Natural Enemies. New York: Cambridge University Press.Google Scholar
Denoth, M., Frid, L. & Myers, J. H. (2002). Multiple agents in biological control: improving the odds?Biological Control, 24, 20–30.CrossRefGoogle Scholar
Eubanks, M. D. & Denno, R. F. (2000). Host plants mediate ominivore–herbivore interactions and influence prey suppression. Ecology, 81, 936–947.Google Scholar
Evans, E. W. (1991). Intra versus interspecific interactions of ladybeetles (Coleoptera: Coccinellidae) attacking aphids. Oecologia, 87, 401–408.CrossRefGoogle ScholarPubMed
Evans, E. W. & Youssef, N. N. (1992). Numerical responses of aphid predators to varying prey density among Utah alfalfa fields. Journal of the Kansas Entomological Society, 65, 30–38.Google Scholar
Finke, D. L. & Denno, R. F. (2004). Predator diversity dampens trophic cascades. Nature, 429, 407– 410.CrossRefGoogle ScholarPubMed
Frazer, B. D. & Gill, B. (1981). Hunger, movement and predation of Coccinella californica on pea aphids in the laboratory and in the field. Canadian Entomologist, 113, 1025–1033.CrossRefGoogle Scholar
Godfray, H. C. J. & Pacala, S. W. (1992). Aggregation and the population dynamics of parasitoids and predators. American Naturalist, 140, 30–40.CrossRefGoogle ScholarPubMed
Gross, K. & Ives, A. R. (1999). Inferring host–parasitoid stability from patterns of parasitism among patches. American Naturalist, 154, 489–496.Google ScholarPubMed
Gross, K., Ives, A. R. & Nordheim, E. V. (2005). Estimating time-varying vital rates from observation time series: a case study in aphid biological control. Ecology, 86, 740–752.CrossRefGoogle Scholar
Hairston, N. G. Jr. & Hairston, N. G. Sr. (1993). Cause–effect relationships in energy flow, trophic structure, and interspecies interactions. American Naturalist, 142, 379–411.CrossRefGoogle Scholar
Hairston, N. G. & Hairston, N. G. Sr. (1997). Does food-web complexity eliminate trophic-level dynamics?American Naturalist, 149, 1001–1007.CrossRefGoogle ScholarPubMed
Hairston, N. G., Smith, F. E. & Slobodkin, L. B. (1960). Community structure, population control and competition. American Naturalist, 94, 421–425.CrossRefGoogle Scholar
Harmon, J. P. & Andow, D. A. (2004). Indirect effects between shared prey: predictions for biological control. BioControl, 49, 605–626.CrossRefGoogle Scholar
Hassell, M. P. (1978). The Dynamics of Arthropod Predator–Prey Systems. Princeton, NJ: Princeton University Press.Google ScholarPubMed
Hassell, M. P. & May, R. M. (1973). Stability in insect host–parasite models. Journal of Animal Ecology, 42, 693–736.CrossRefGoogle Scholar
Hassell, M. P. & May, R. M. (1974). Aggregation in predators and insect parasites and its effect on stability. Journal of Animal Ecology, 43, 567–594.CrossRefGoogle Scholar
Hassell, M. P., May, R. M., Pacala, S. W. & Chesson, P. L. (1991). The persistence of host–parasitoid associations in patchy environments. I. A general criterion. American Naturalist, 138, 568–583.CrossRefGoogle Scholar
Hawkins, B.A., Mills, N. J., Jervis, M. A. & Price, P. W. (1999). Is the biological control of insects a natural phenomenon?Oikos, 86, 493–506.CrossRefGoogle Scholar
Hodek, I. & Honek, A. (1996). Ecology of Coccinellidae. Boston, MA: Kluwer.CrossRefGoogle Scholar
Hole, D. G., Perkins, A. J., Wilson, J. D.et al. (2005). Does organic farming benefit biodiversity?Biological Conservation, 122, 113–139.CrossRefGoogle Scholar
Holt, R. D. (1977). Predation, apparent competition, and the structure of prey communities. Theoretical Population Biology, 12, 197–229.CrossRefGoogle ScholarPubMed
Huffaker, C. B. (1958). Experimental studies on predation: dispersion factors and predator–prey oscillations. Hilgardia, 27, 343–383.CrossRefGoogle Scholar
Ives, A. R. (1992a). Continuous-time models of host–parasitoid interactions. American Naturalist, 140, 1–29.CrossRefGoogle ScholarPubMed
Ives, A. R. (1992b). Density-dependent and density-independent parasitoid aggregation in model host–parasitoid systems. American Naturalist, 140, 912– 937.CrossRefGoogle Scholar
Ives, A. R. (1995). Spatial heterogeneity and host–parasitoid population dynamics: do we need to study behavior?Oikos, 74, 366–376.CrossRefGoogle Scholar
Ives, A. R., Cardinale, B. J. & Snyder, W. E. (2005). A synthesis of subdisciplines: predator–prey interactions, and biodiversity and ecosystem functioning. Ecology Letters, 8, 102–116.CrossRefGoogle Scholar
LaMana, M. L. & Miller, J. C. (1996). Field observations on Harmonia axyridis Pallas (Coleoptera: Coccinellidae) in Oregon. Biological Control, 6, 232–237.CrossRefGoogle Scholar
Landis, D. A., Wratten, S. D. & Gurr, G. M. (2000). Habitat management to conserve natural enemies of arthropod pests in agriculture. Annual Review of Entomology, 45, 175–201.CrossRefGoogle ScholarPubMed
Lattin, J. D. (1989). Bionomics of the Nabidae. Annual Review of Entomology, 34, 383–400.CrossRefGoogle Scholar
Losey, J. E. & Denno, R. F. (1998). Positive predator–predator interactions: enhanced predation rates and synergistic suppression of aphid populations. Ecology, 79, 2143–2152.Google Scholar
Mackauer, M. & Kambhampati, S. (1986). Structural changes in the parasite guild attacking the pea aphid in North America. In Ecology of Aphidophaga, ed. Hodek, I., pp. 347–356. Prague, Czechoslovakia: Academia.Google Scholar
Montoya, J. M., Rodríguez, M. A. & Hawkins, B. A. (2003). Food web complexity and higher-level ecosystem services. Ecology Letters, 6, 587–593.CrossRefGoogle Scholar
Murdoch, W. W. & Briggs, C. J. (1997). Theory for biological control: recent developments. Ecology, 77, 2001–2013.CrossRefGoogle Scholar
Murdoch, W. W., Nisbet, R. M., Luck, R. F., Godfray, H. C. J. & Gurney, W. S. C. (1992). Size-selective sex-allocation and host feeding in a parasitoid host model. Journal of Animal Ecology, 61, 533–541.CrossRefGoogle Scholar
Murdoch, W. W., Briggs, C. J. & Nisbet, R. M. (2003). Consumer-Resource Dynamics. Princeton, NJ: Princeton University Press.Google Scholar
Murdoch, W., Briggs, C. J. & Swarbrick, S. (2005). Host suppression and stability in a parasitoid–host system: experimental demonstration. Science, 309, 610–613.CrossRefGoogle Scholar
Myers, J. H., Higgins, C. & Kovacs, E. (1989). How many insect species are necessary for the biological control of insects?Environmental Entomology, 18, 541–547.CrossRefGoogle Scholar
Nicholson, A. J. & Bailey, V. A. (1935). The balance of animal populations. Proceedings of the Zoological Society of London, 43, 551–598.CrossRefGoogle Scholar
Olson, A. C., Ives, A. R. & Gross, K. (2000). Spatially aggregated parasitism on pea aphids, Acyrthosiphon pisum, caused by random foraging behavior of the parasitoid Aphidius ervi. Oikos, 91, 66–76.CrossRefGoogle Scholar
Östman, Ö. & Ives, A. R. (2003). Scale-dependent indirect interactions between two prey species through a shared predator. Oikos, 102, 505–514.Google Scholar
Pimentel, D. (1961). Species diversity and insect population outbreaks. Annals of the Entomological Society of America, 54, 76–86.CrossRefGoogle Scholar
Polis, G. A. (1991). Complex trophic interactions in deserts: an empirical critique of food-web theory. American Naturalist, 138, 123–155.CrossRefGoogle Scholar
Polis, G. A. & Strong, D. R. (1996). Food web complexity and community dynamics. American Naturalist, 147, 813–846.CrossRefGoogle Scholar
Polis, G. A., Myers, C. A. & Holt, R. D. (1989). The ecology and evolution of intraguild predation: potential competitors that eat each other. Annual Review of Ecology and Systematics, 20, 297–330.CrossRefGoogle Scholar
Prasad, R. P. & Snyder, W. E. (2006). Polyphagy complicates conservation biological control that targets generalist predators. Journal of Applied Ecology, 43, 343–352.CrossRefGoogle Scholar
Rauwald, K. S. & Ives, A. R. (2001). Biological control in disturbed agricultural systems and the rapid re-establishment of parasitoids. Ecological Applications, 11, 1224–1234.CrossRefGoogle Scholar
Reeve, J. D. (1988). Environmental variability, migration and persistence in host–parasitoid systems. American Naturalist, 132, 810–836.CrossRefGoogle Scholar
Root, R. B. (1973). Organization of a plant–arthropod association in simple and diverse habitats: the fauna of collards. Ecological Monographs, 43, 95–124.CrossRefGoogle Scholar
Rosenheim, J. A., Wilhoit, L. R. & Armer, C. A. (1993). Influence of intraguild predation among generalist insect predators on the suppression of an herbivore population. Oecologia, 96, 439–449.CrossRefGoogle ScholarPubMed
Rosenheim, J. A., Kaya, H. K., Ehler, L. E., Marois, J. J. & Jaffee, B. A. (1995). Intraguild predation among biological-control agents: theory and practice. Biological Control, 5, 303–335.CrossRefGoogle Scholar
Schmitz, O. J. (2005). Behaviors of predators and prey and links with population-level processes. In Ecology of Predator–Prey Interactions, eds. Barbosa, P. & Castellanos, I., pp. 256–278. New York: Oxford University Press.Google Scholar
Settle, W. H., Ariawan, H., Astuti, E. T.et al. (1996). Managing tropical rice pests through conservation of generalist natural enemies and alternative prey. Ecology, 77, 1975–1988.CrossRefGoogle Scholar
Sih, A., Englund, G. & Wooster, D. (1998). Emergent impacts of multiple predators on prey. Trends in Ecology and Evolution, 13, 350–355.CrossRefGoogle ScholarPubMed
Snyder, W. E. & Ives, A. R. (2003). Interactions between specialist and generalist natural enemies: parasitoids, predators, and pea aphid biocontrol. Ecology, 84, 91–107.CrossRefGoogle Scholar
Straub, C. S., Finke, D. L. & Snyder, W. E. (2008) Are the conservation of natural enemy biodiversity and biological control compatible goals?Biological Control, 45, 225–237.CrossRefGoogle Scholar
Strong, D. R. (1992). Are trophic cascades all wet? Differentiation and donor-control in speciose systems. Ecology, 73, 747–754.CrossRefGoogle Scholar
Symondson, W. O. C., Sunderland, K. D. & Greenstone, M. H. (2002). Can generalist predators be effective biocontrol agents?Annual Review of Entomology, 47, 561–594.CrossRefGoogle ScholarPubMed
Tscharntke, T., Klein, A., M. Kruess, A., Steffan-Dewenter, I. & Thies, C. (2005). Landscape perspectives on agricultural intensification and biodiversity – ecosystem service management. Ecology Letters, 8, 857–874.CrossRefGoogle Scholar
Turchin, P. (2003). Complex Population Dynamics: A Theoretical/Empirical Synthesis. Princeton, NJ: Princeton University Press.Google Scholar
Emden, H. F. & Williams, G. F. (1974). Insect stability and diversity in agro-ecosystems. Annual Review of Entomology, 19, 455–475.CrossRefGoogle Scholar
Wilby, A. & Thomas, M. B. (2002). Natural enemy diversity and pest control: patterns of pest emergence with agricultural intensification. Ecology Letters, 45, 353–360.CrossRefGoogle Scholar
Wilby, A., Villareal, S. C., Lan, L. P., Heong, K. L. & Thomas, M. B. (2005). Functional benefits of predator species diversity depend on prey identity. Ecological Entomology, 30, 497–501.CrossRefGoogle Scholar
Yasuda, H., Evans, E. W., Kajita, Y., Urakawa, K. & Takizawa, T. (2004). Asymmetric larval interactions between introduced and indigenous ladybirds in North America. Oecologia, 141, 722–731.CrossRefGoogle ScholarPubMed

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