Skip to main content Accessibility help
×
Hostname: page-component-8448b6f56d-tj2md Total loading time: 0 Render date: 2024-04-19T14:54:37.766Z Has data issue: false hasContentIssue false

13 - Ecosystems: concepts, analyses, and practical implications in IPM

Published online by Cambridge University Press:  04 August 2010

Marcos Kogan
Affiliation:
Oregon State University
Paul Jepson
Affiliation:
Oregon State University
Get access

Summary

Introduction

A major principle of integrated pest management (IPM) is that strategies and tactics be consistent with ecological processes. IPM advanced traditional pest control by recognizing economic thresholds (below which population size does not warrant suppression), and addressing aspects of herbivore–plant and predator–prey interactions amenable to manipulation for pest control purposes. However, the premise that herbivorous insects and pathogens in general are detrimental to plant growth and reproduction has persisted.

In recent years, our perspective of insect herbivores has begun to change from this traditional view to a view that recognizes the role of native insect herbivores in maintaining plant productivity, vegetative diversity, and other ecosystem properties at ecosystem carrying capacity. Recent advances in studies of integrated ecosystems has led to an emerging view of herbivores as a negative feedback (regulatory) mechanism, triggered by environmental changes, that may stabilize ecosystem structure and function in natural ecosystems.

Commodity systems are maintained intentionally in an artificial condition to maximize commodity production, generally on an annual basis. This triggers herbivore responses to resource quality or abundance that may be undesirable for some management goals. Nevertheless, understanding the factors that trigger herbivore outbreaks and their consequences for ecosystems conditions can lead to improved management decisions, particularly strategies for preventing outbreaks and methods for evaluating the need for pest suppression, consistent with the objective that IPM supports ecological principles. IPM tactics will still be necessary, especially in the artificial environment of crop systems, or for managing exotic pests.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2007

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Alfaro, R. I. and Shepherd, R. F. (1991). Tree-ring growth of interior Douglas-fir after one year's defoliation by Douglas-fir tussock moth. Forest Science, 37, 959–64.Google Scholar
Alstad, D. N. and Andow, D. A. (1995). Managing the evolution of insect resistance to transgenic plants. Science, 268, 1894–6.CrossRefGoogle ScholarPubMed
Bernays, E. A. and Chapman, R. F. (1994). Host-Plant Selection by Phytophagous Insects. New York: Chapman & Hall.CrossRefGoogle Scholar
Cardé, R. T. (1996). Odour plumes and odour-mediated flight in insects. In Olfaction in Mosquito–Host Interactions (Ciba Foundation Symposium 200). Chichester, UK: John Wiley and Sons. pp. 54–70.Google Scholar
Coley, P. D., Bryant, J. P. and Chapin, F. S. III (1985). Resource availability and plant antiherbivore defense. Science, 230, 895–9.CrossRefGoogle ScholarPubMed
Courtney, S. P. (1985). Apparency in coevolving relationships. Oikos, 44, 91–8.CrossRefGoogle Scholar
Davidson, D. W. (1993). The effects of herbivory and granivory on terrestrial plant succession. Oikos, 68, 23–35.CrossRefGoogle Scholar
Dolch, R. and Tscharntke, T. (2000). Defoliation of alders (Alnus glutinosa) affects herbivory by leaf beetles on undamaged neighbors. Oecologia, 125, 504–11.CrossRefGoogle Scholar
Dubbert, M., Tscharntke, T. and Vidal, S. (1998). Stem-boring insects of fragmented Calamagrostis habitats: herbivore–parasitoid community structure and the unpredictability of grass shoot abundance. Ecological Entomology, 23, 271–80.CrossRefGoogle Scholar
Dyer, M. I., Turner, C. L. and Seastedt, T. R. (1993). Herbivory and its consequences. Ecological Applications, 3, 10–16.CrossRefGoogle ScholarPubMed
Dyer, M. I., Moon, A. M., Brown, M. R. and Crossley, D. A. Jr. (1995). Grasshopper crop and midgut extract effects on plants: an example of reward feedback. Proceedings of the National Academy of Sciences USA, 92, 5475–8.CrossRefGoogle ScholarPubMed
Farmer, E. E. and Ryan, C. A. (1990). Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves. Proceedings of the National Academy of Sciences USA, 87, 7713–16.CrossRefGoogle ScholarPubMed
Garrett, K. A. and Mundt, C. C. (2000 a). Host diversity can reduce potato late blight severity for focal and general patterns of primary inoculum. Phytopathology, 90, 1307–12.CrossRefGoogle ScholarPubMed
Garrett, K. A. and Mundt, C. C. (2000 b). Effects of planting density and the composition of wheat cultivar mixtures on stripe rust: an analysis taking into account limits to the replication of controls. Phytopathology, 90, 1313–21.CrossRefGoogle ScholarPubMed
Georgiadis, N. J. and McNaughton, S. J. (1988). Interactions between grazers and a cyanogenic grass, Cynodon plectostachyus. Oikos, 51, 343–50.CrossRefGoogle Scholar
Harborne, J. B. (1994). Introduction to Ecological Biochemistry, 4th edn. London: Academic Press.Google Scholar
Holling, C. S. (1959). Some characteristics of simple types of predation and parasitism. Canadian Entomologist, 91, 385–98.CrossRefGoogle Scholar
House, G. J. and Stinner, B. R. (1987). Arthropods in Conservation Tillage Systems (Miscellaneous Publications, No. 65). Lanham, MD: Entomological Society of America.Google Scholar
Hunter, M. D. and Price, P. W. (1992). Playing chutes and ladders: heterogeneity and the relative roles of bottom-up and top-down forces in natural communities. Ecology, 73, 724–32.Google Scholar
Ingham, R. E., Trofymow, J. A., Ingham, E. R. and Coleman, D. C. (1985). Interactions of bacteria, fungi, and their nematode grazers: effects on nutrient cycling and plant growth. Ecological Monographs, 55, 119–40.CrossRefGoogle Scholar
Kareiva, P. (1983). Influence of vegetation texture on herbivore populations: resource concentration and herbivore movement. In Denno, R. F. and McClure, M. S. (eds.), Variable Plants and Herbivores in Natural and Managed Systems. New York: Academic Press. pp. 259–89.Google Scholar
Knapp, A. K. and Seastedt, T. R. (1986). Detritus accumulation limits productivity of tallgrass prairie. BioScience, 36, 662–8.CrossRefGoogle Scholar
Kogan, M. (1975). Plant resistance in pest management. In Metcalf, R. L. and Luckmann, W. H. (eds)., Introduction to Insect Pest Management. New York: Wiley. pp. 103–46.Google Scholar
Kruess, A. and Tscharntke, T. (1994). Habitat fragmentation, species loss, and biological control. Science, 264, 1581–4.CrossRefGoogle ScholarPubMed
Kruess, A. and Tscharntke, T. (2000). Species richness and parasitism in a fragmented landscape: experiments and field studies with insects on Vicia sepium. Oecologia, 122, 129–37.CrossRefGoogle Scholar
Mattson, W. J. and Addy, N. D. (1975). Phytophagous insects as regulators of forest primary production. Science, 190, 515–22.CrossRefGoogle Scholar
Mattson, W. J. and Haack, R. A. (1987). The role of drought in outbreaks of plant-eating insects. BioScience, 37, 110–18.CrossRefGoogle Scholar
Miller, G. E. (1983). Evaluation of the effectiveness of cold-water misting of trees in seed orchards for control of Douglas-fir cone gall midge (Diptera: Cecidomyiidae). Journal of Economic Entomology, 76, 916–19.CrossRefGoogle Scholar
Pedigo, L. P., Hutchins, S. H. and Higley, L. G. (1986). Economic injury levels in theory and practice. Annual Review of Entomology, 31, 341–68.CrossRefGoogle Scholar
Risch, S. (1980). The population dynamics of several herbivorous beetles in a tropical agroecosystem: the effect of intercropping corn, beans and squash in Costa Rica. Journal of Applied Ecology, 17, 593–612.CrossRefGoogle Scholar
Risch, S. J. (1981). Insect herbivore abundance in tropical monocultures and polycultures: an experimental test of two hypotheses. Ecology, 62, 1325–40.CrossRefGoogle Scholar
Roland, J. (1993). Large-scale forest fragmentation increases the duration of tent caterpillar outbreak. Oecologia, 93, 25–30.CrossRefGoogle ScholarPubMed
Roland, J. and Taylor, P. D. (1997). Insect parasitoid species respond to forest structure at different spatial scales. Nature, 386, 710–13.CrossRefGoogle Scholar
Romme, W. H., Knight, D. H. and Yavitt, J. B. (1986). Mountain pine beetle outbreaks in the Rocky Mountains: regulators of primary productivity?American Naturalist, 127, 484–94.CrossRefGoogle Scholar
Schowalter, T. D. (1985). Adaptations of insects to disturbance. In Pickett, S. T. A. and White, P. S. (eds.), The Ecology of Natural Disturbance and Patch Dynamics. Orlando, FL: Academic Press. pp. 235–52.Google Scholar
Schowalter, T. D. (2000 a). Insect Ecology: An Ecosystem Approach. San Diego, CA: Academic Press.Google Scholar
Schowalter, T. D. (2000 b). Insects as regulators of ecosystem development. In Coleman, D. C. and Hendrix, P. F. (eds.), Invertebrates as Webmasters in Ecosystems. Wallingford, UK: CAB International. pp. 99–114.CrossRefGoogle Scholar
Schowalter, T. D. and Stein, J. D. (1987). Influence of Douglas-fir seedling provenance and proximity to insect population sources on susceptibility to Lygus hesperus (Heteroptera: Miridae) in a forest nursery in western Oregon. Environmental Entomology, 16, 984–6.CrossRefGoogle Scholar
Schowalter, T. D. and Turchin, P. (1993). Southern pine beetle infestation development: interaction between pine and hardwood basal areas. Forest Science, 39, 201–10.Google Scholar
Schowalter, T. D. and Withgott, J. (2001). Rethinking insects: what would an ecosystem approach look like?Conservation Biology in Practice, 2, 10–16.CrossRefGoogle Scholar
Schowalter, T. D., Sabin, T. E., Stafford, S. G. and Sexton, J. M. (1991). Phytophage effects on primary production, nutrient turnover, and litter decomposition of young Douglas-fir in western Oregon. Forest Ecology and Management, 42, 229–43.CrossRefGoogle Scholar
Schowalter, T. D., Lightfoot, D. C. and Whitford, W. G. (1999). Diversity of Arthropod Responses to Host-Plant Water Stress in a Desert Ecosystem in Southern New Mexico. American Midland Naturalist, 142, 281–90.CrossRefGoogle Scholar
Schultz, J. C. (1983). Habitat selection and foraging tactics of caterpillars in heterogeneous trees. In Denno, R. F. and McClure, M. S. (eds.), Variable Plants and Herbivores in Natural and Managed Systems. New York: Academic Press. pp. 61–90.Google Scholar
Seastedt, T. R. (1985). Maximization of primary and secondary productivity by grazers. American Naturalist, 126, 559–64.CrossRefGoogle Scholar
Setälä, H. and Huhta, V. (1991). Soil fauna increase Betula pendula growth: laboratory experiments with coniferous forest floor. Ecology, 72, 665–71.CrossRefGoogle Scholar
Stanton, M. L. (1983). Spatial patterns in the plant community and their effects upon insect search. In Ahmad, S. (ed.), Herbivorous Insects: Host-Seeking Behavior and Mechanisms. New York: Academic Press. pp. 125–57.Google Scholar
Steffan-Dewenter, I. and Tscharntke, T. (1999). Effects of habitat isolation on pollinator communities and seed set. Oecologia, 121, 432–40.CrossRefGoogle ScholarPubMed
Tabashnik, B. E. (1994). Evolution of resistance to Bacillus thuringiensis. Annual Review of Entomology, 39, 47–79.CrossRefGoogle Scholar
Tanada, Y. and Kaya, H. (1993). Insect Pathology. San Diego, CA: Academic Press.Google Scholar
Thies, C. and Tscharntke, T. (1999). Landscape structure and biological control in agroecosystems. Science, 285, 893–5.CrossRefGoogle ScholarPubMed
Trumble, J. T., Kolodny-Hirsch, D. M. and Ting, I. P. (1993). Plant compensation for arthropod herbivory. Annual Review of Entomology, 38, 93–119.CrossRefGoogle Scholar
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, 1251–3.CrossRefGoogle ScholarPubMed
Bosch, R., Messinger, P. S. and Gutierrez, A. P. (1982). An Introduction to Biological Control. New York: Plenum Press.CrossRefGoogle Scholar
Driesche, R. G. and Bellows, T. (1996). Biological Control. New York: Chapman and Hall.CrossRefGoogle Scholar
Visser, J. H. (1986). Host odor perception in phytophagous insects. Annual Review of Entomology, 31, 121–44.CrossRefGoogle Scholar
Waring, G. L. and Cobb, N. S. (1992). The impact of plant stress on herbivore population dynamics. In Bernays, E. A. (ed.), Plant–Insect Interactions (Vol. 4), Boca Raton, FL: CRC Press. pp. 167–226.Google Scholar
White, T. C. R. (1969). An index to measure weather-induced stress of trees associated with outbreaks of psyllids in Australia. Ecology, 50, 905–9.CrossRefGoogle Scholar
White, T. C. R. (1976). Weather, food and plagues of locusts. Oecologia, 22, 119–34.CrossRefGoogle ScholarPubMed
White, T. C. R. (1984). The abundance of invertebrate herbivores in relation to the availability of nitrogen in stressed food plants. Oecologia, 63, 90–105.CrossRefGoogle ScholarPubMed
Williamson, S. C., Detling, J. K., Dodd, J. L. and Dyer, M. I. (1989). Experimental evaluation of the grazing optimization hypothesis. Journal of Range Management, 42, 149–52.CrossRefGoogle Scholar
Zabel, J. and Tscharntke, T. (1998). Does fragmentation of Urtica habitats affect phytophagous and predatory insects differentially?Oecologia, 116, 419–25.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×