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The Lotka–Volterra predator-prey model makes a number of assumptions about the environment and biology of the predator and prey populations: [5] The prey population finds ample food at all times. The food supply of the predator population depends entirely on the size of the prey population.
The prey does not have to be attracted towards the predator for the predator to benefit: it is sufficient for the predator simply not to be identified as a threat. Wicklerian-Eisnerian mimics may resemble a mutualistic ally, or a species of little significance to the prey such as a commensal. [9]
A trophic function was first introduced in the differential equations of the Kolmogorov predator–prey model. It generalizes the linear case of predator–prey interaction firstly described by Volterra and Lotka in the Lotka–Volterra equation. A trophic function represents the consumption of prey assuming a given number of predators.
This model can be generalized to any number of species competing against each other. One can think of the populations and growth rates as vectors, α 's as a matrix.Then the equation for any species i becomes = (=) or, if the carrying capacity is pulled into the interaction matrix (this doesn't actually change the equations, only how the interaction matrix is defined), = (=) where N is the ...
Because the number of prey harvested by each predator decreases as predators become more dense, ratio-dependent predation is a way of incorporating predator intraspecific competition for food. Ratio-dependent predation may account for heterogeneity in large-scale natural systems in which predator efficiency decreases when prey is scarce. [1]
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 solution to these equations in the simple one-predator species, one-prey species model is a stable linked oscillation of population levels for both predator and prey. However, when time lags between respective population growths are modeled, these oscillations will tend to amplify, eventually leading to extinction of both species.
One classical version of the optimal foraging theory is the optimal diet model, which is also known as the prey choice model or the contingency model. In this model, the predator encounters different prey items and decides whether to eat what it has or search for a more profitable prey item. The model predicts that foragers should ignore low ...