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The diversity of interactions between herbivores and plants, between predators and prey, and between parasites, parasitoids, pathogens, and hosts can be grouped under the heading of exploitation—interactions between species that enhance the fitness of one individual at the expense of another.

Exploitation weaves populations into a web of relationships that defy easy generalization. The number of exploitative interactions between species far exceeds the number of species in the biosphere, and the nature of exploitation goes far beyond the typical consumption of one organism by another. For instance, many parasites and pathogens manipulate host behavior to enhance their own fitness at the expense of the host. Spiny-headed worms alter the behavior of a variety of crustacean hosts in a way that increases the probability that the one host species will be eaten by another. A pathogenic fungus manipulates the growth program of its host plant in a way to produce "pseudoflowers," structures aimed at promoting the reproduction of the pathogen. In the process the pathogen usually kills the host plant and always renders it sterile. Predation by one flour beetle species on another can be used as a potent means of interference competition except in the presence of a protozoan parasite, which seems to give a competitive advantage to less predaceous species.

Predators, parasites, and pathogens influence the distribution, abundance, and structure of prey and host populations. Herbivorous stream insects have been shown to control the density of their agal and bacterial food. The herbivorous moth larva Cactoblastis cactorum combined with pathogenic microbes reduced the coverage of prickly pear cactus in Australia from millions of hectares to a few thousand. A parasitic infestation reduced the red fox population in Sweden by 70%, which in turn led to increases in the abundance of several prey species eaten by foxes. This parasitic disease revealed the influence of a predator on its prey populations.

Predator-prey, parasite-host, and host-pathogen relationships are dynamic. Populations of a wide variety of predators and prey show highly dynamic fluctuations in abundance ranging from days to decades. A particularly well-studied example of predator-prey cycles is that of snowshoe hares and their predators, which have been shown to result from the combined effects of the snowshoe hares on their food and of the predators on the snowshoe hare population. Mathematical models of predator-prey interactions by Lotka and Volterra suggest that exploitative interactions themselves can produce population cycles without any influences from outside forces such as weather. Predator-prey cycles have also been observed in a few laboratory populations under restricted circumstances.

To persist in the face of exploitation, hosts and prey need refuges. The refuges that promote the persistence of hosts and prey include secure places to which the exploiter has limited access. However, living in large groups can be considered as a kind of refuge since it reduces the probability that an individual host or prey will be attacked. It appears that predator satiation is a defensive tactic used by a wide variety of organisms from rain forest trees to temperate insects. Growing to large size can also represent a kind of refuge when the prey species is faced by size-selective predators. Size is used as a refuge by prey species ranging from stream insects and intertidal invertebrates to rhinoceros.

Predators and parasites have been used to control populations of insects that attack crops or to control invasive weeds. Recent research in Kenya has shown that a crayfish, Procambarus clarkii, controls the snails that act as intermediate hosts for Schistosoma, a highly pathogenic human parasite. Preliminary results indicate that crayfish successfully control host snails in the artificial impoundments used for livestock watering and domestic water, important sources of infection by Schistosoma.







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