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Chapter 13 - Predation and Other Exploitative Interactions

from Part IV - Community Ecology

Published online by Cambridge University Press:  04 April 2024

Fred D. Singer
Affiliation:
Radford University, Virginia
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Summary

Exploitative interactions can be understood in terms of their lethality and intimacy. Predators and parasitoids cause highest lethality, parasites and parasitoids have highest intimacy with their hosts, while grazers are low on both scales. Exploiters can regulate the populations of their hosts directly by killing or injuring them, or through nonconsumptive processes such as increasing their prey’s stress level and thereby reducing reproductive rates, as has been implicated for the snowshoe hare. Exploiters can also regulate community processes indirectly; for example bats and birds eat arthropods in the forest, which reduces leaf damage by herbivorous arthropods. Prey and hosts use constitutive defenses, such as thorns in plants, and large body size in Serengeti grazers, against exploiters. Some species have evolved induced defenses; for example some plants release toxic chemicals following herbivore attack. The outcomes of exploitative interactions can be predicted by the Lotka–Volterra predation model, which, in its most basic form, predicts that the relative abundance of predators and prey will cycle. A simple model of disease transmission can explain how disease spreads in host populations based on the ease of transmission, the amount of time the host is infectious, and the population size of the host. Both models make numerous simplifying assumptions. Ecologists can incorporate biological complexity into these models, which makes them more realistic, but also more difficult to understand and apply.

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Ecology in Action , pp. 328 - 353
Publisher: Cambridge University Press
Print publication year: 2024

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References

Further Reading

Connolly, B. M., Pearson, D. E., and Mack, R. N. 2014. Granivory of invasive, naturalized, and native plants in communities differentially susceptible to invasion. Ecology 95: 17591769.CrossRefGoogle Scholar
Decaestecker, E., Gaba, S., Raeymaekers, J. A., et al. 2007. Host–parasite “Red Queen” dynamics archived in pond sediment. Nature 450: 870873.CrossRefGoogle ScholarPubMed
Snedden, C. E., Makanani, S. K., Schwartz, S. T., et al. 2021. SARS-CoV-2: Cross-scale insights from ecology and evolution. Trends in Microbiology 29: 593605.CrossRefGoogle ScholarPubMed
Sugimoto, K., Matsui, K., Iijima, Y., et al. 2014. Intake and transformation to a glycoside of (Z)-3-hexenol from infested neighbors reveals a mode of plant odor reception and defense. Proceedings of the National Academy of Sciences 111: 71447149.CrossRefGoogle ScholarPubMed
Wilson, A. M., Hubel, T. Y., Wilshin, S. D., et al. 2018. Biomechanics of predator–prey arms race in lion, zebra, cheetah and impala. Nature 544: 183188.CrossRefGoogle Scholar

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