Paradox of the pesticides

The paradox of the pesticides is a paradox that states that applying pesticide to a pest may end up increasing the abundance of the pest if the pesticide upsets natural predator–prey dynamics in the ecosystem.

The paradox can occur only when the target pest has a naturally occurring predator that is equally affected by the pesticide. It therefore presents a case for more specialized pesticide products.

Lotka–Volterra equation

To describe the paradox of the pesticides mathematically, the Lotka–Volterra equation, a set of first-order, nonlinear, differential equations, which are frequently used to describe predator–prey interactions, can be modified to account for the additions of pesticides into the predator–prey interactions.

Without pesticides

The variables represent the following:

The following two equations are the original Lotka–Volterra equation, which describe the rate of change of each respective population as a function of the population of the other organism:

By setting each equation to zero and thus assuming a stable population, a graph of two lines (isoclines) can be made to find the equilibrium point, the point at which both interacting populations are stable.

These are the isoclines for the two above equations:

Accounting for pesticides

Predator–prey isoclines before and after pesticide application. Pest abundance has increased.

Now, to account for the difference in the population dynamics of the predator and prey that occurs with the addition of pesticides, variable q is added to represent the per capita rate at which both species are killed by the pesticide. The original Lotka–Volterra equations change to be as follows:

Solving the isoclines as was done above, the following equations represent the two lines with the intersection that represents the new equilibrium point. These are the new isoclines for the populations:

As one can see from the new isoclines, the new equilibrium will have a higher H value and a lower P value so the number of prey will increase while the number of predator decreases. Thus, prey, which is normally the targeted by the pesticide, is actually being benefited instead of harmed by the pesticide.

A credible, simple alternative to the Lotka-Volterra predator–prey model and its common prey dependent generalizations is the ratio dependent or Arditi–Ginzburg model.[1] The two are the extremes of the spectrum of predator interference models. According to the authors of the alternative view, the data show that true interactions in nature are so far from the Lotka-Volterra extreme on the interference spectrum that the model can simply be discounted as wrong. They are much closer to the ratio-dependent extreme, so if a simple model is needed, one can use the Arditi–Ginzburg model as the first approximation.[2]

Empirical evidence

The paradox has been documented repeatedly throughout the history of pest management. Predatory mites, for example, naturally prey upon phytophagous mites, which are common pests in apple orchards. Spraying the orchards kills both mites, but the effect of diminished predation is larger than that of the pesticide, and phytophagous mites increase in abundance.[3]

The effect has also been seen on rice, as documented by the International Rice Research Institute, which noted significant declines in pest populations when they stopped applying pesticide.[4]

Related phenomena

Recent studies suggest that such a paradox might not be necessarily caused by the reduction of the predator population by harvesting itself, for example, by a pesticide. The host population is reduced at the moment of harvesting, and simultaneously, the intraspecific density effect is weakened.[5] Intraspecific competition accounts for the competition between individuals of a same species. When the population density is high and resources are consequently relatively scarce, each individual has less access to resources to invest energy in growth, survivorship and reproduction. That causes a decrease in the survival rate or an increase in mortality.

Intraspecific competition increases with density. One could expect that a population decrease (due to harvesting, for example) will decrease the population density and reduce intraspecific competition, which would lead to a lower death rate among the prey population.

Studies show also that direct effects on the predator population, through harvesting of the prey, are not necessary to observe the paradox.[5] Harvesting of prey has been shown to trigger a reduction in the predator’s reproduction rate, which lowers the equilibrium predator level. Thus, changes in life history strategy (patterns of growth, reproduction and survivorship) can also contribute to the paradox.

Seemingly the paradox can be accounted for by the indirect effects of harvesting on the native ecological interactions of prey and predator: reduction of intraspecific density effect for the prey and reduction of the reproductive rate for the predator. The former increases the population recovery of the prey, and the latter decreases the equilibrium population level for the predator.

Implications

The paradox implies the need for more specialized pesticides that are tailored to the target pest. If the pesticide can effectively reduce only the prey population, the predator population will remain largely unaffected except for the change in its food supply. Broad-spectrum pesticides are more likely to induce the paradox and cause an increase in target pest population by killing its predators as well. In certain cases, however, if the predator is closely related to the target pest, even narrow-spectrum pesticides may be insufficient.

Solutions

To deal with the paradox, growers may turn to integrated pest management (IPM),[6] an ecological approach to pest control that accounts for the interactions between pests and their environment.[7] There is not only one way to practice IPM, but some methods include using mechanical trapping devices or increasing the abundance of natural predators.[8]

IPM is also often touted for its environmental and health benefits, as it avoids the use of chemical pesticides.

See also

References

  1. ↑ Arditi, R. and Ginzburg, L.R. 1989. Coupling in predator–prey dynamics: ratio dependence. Journal of Theoretical Biology 139: 311-326.
  2. ↑ Arditi, R. and Ginzburg, L.R. 2012. How Species Interact: Altering the Standard View on Trophic Ecology. Oxford University Press, New York, NY.
  3. ↑ Lester, P. J.; Thistlewood, H. M. A.; Harmsen, R. (1998). "The Effects of Refuge Size and Number on Acarine Predator–Prey Dynamics in a Pesticide-Disturbed Apple Orchard". Journal of Applied Ecology. 35 (2): 323–331. doi:10.1046/j.1365-2664.1998.00304.x. JSTOR 2405131.
  4. ↑ Sackville Hamilton, Henry (January–March 2008). "The Pesticide Paradox" (PDF). Rice Today (1): 32–33. Retrieved 3 February 2011.
  5. 1 2 Matsuoka, T.; Seno, H. (2008). "Ecological balance in the native population dynamics may cause the paradox of pest control with harvesting". Journal of Theoretical Biology. 252 (1): 87–97. doi:10.1016/j.jtbi.2008.01.024. PMID 18329048.
  6. ↑ "Michigan Tech Blog: 6 Advantages of Integrated Pest Management" https://hub.sfi.mtu.edu/members/3137/blog/2015/Jan/5-advantages-of-integrated-pest-management
  7. ↑ U.S. Environmental Protection Agency. “Integrated Pest Management (IPM) Principles,” http://www.epa.gov/opp00001/factsheets/ipm.htm (2008).
  8. ↑ U.S. Environmental Protection Agency. “Pesticides and Food: What ‘Integrated Pest Management’ Means,” http://www.epa.gov/pesticides/food/ipm.htm (2007).
This article is issued from Wikipedia - version of the 10/5/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.