We study a supply chain model which is based on Schnakenberg type kinetics. This model is realistic in a predator-prey context if cooperation of predators is prevalent in the system and if there is practically an unlimited pool of prey, i.e. the predators will not feel the impact of the limited amount of prey due to its large quantity. The system also serves as a model for a sequence of irrever...

We firstly show the permanence of hybrid prey-predator system. Then, when both white and color noises are taken into account, we examine the asymptotic properties of stochastic prey-predator model with Markovian switching. Finally, the optimal harvest policy of stochastic prey-predator model perturbed by white noise is considered.

functional response of stethorus gilvifrons mulsant to varying densities of different developmental stages of eutetranychus orientalis klein was examined in a simplified castor bean leaf disc arena under the laboratory condition. one s.gilvifrons female was isolated individually for 24h with different prey densities (4,8,12,24,48,96,120) at 300c and photoperiod of 14:10 (l:d) h. the number of p...

Resource consumption often increases with greater consumer biodiversity. This could result either from complementarity among consumers or the inclusion of particular key species, and it is often difficult to differentiate between these two mechanisms. We exploited a simple plant mutation (reduced production of surface waxes) to alter foraging within a community of aphid predators, and thus perh...

Sexual dimorphisms in animal vocal behavior have been successfully explained by sexual selection theory (e.g., mammals [1-5]; birds [6, 7]; anurans [8, 9]), but this does not usually include alarm calls, which are thought to be the product of kin or individual selection (e.g., [10, 11]). Here, we present the results of playback experiments with wild Diana monkeys, a species with highly dimorphi...

Similar to the model studied in [11], it is assumed that the parasite under consideration is a microparasite so that the parasite population is not explicitly modeled in the interaction. There are only two interacting species prey and predator in the model. Individuals in each species are classified as either infected or uninfected. Let x1 and x2 denote the uninfected and infected prey populati...

Predation plays a central role in evolutionary processes, but little is known about how predators affect the expression of heritable variation, restricting our ability to predict evolutionary effects of predation. We reared families of three-spined stickleback Gasterosteus aculeatus from two populations-one with a history of fish predation (predator sympatric) and one without (predator naive)-a...

Two or more competing predators can coexist using a single homogeneous prey species if the system containing all three undergoes internally generated fluctuations in density. However, the dynamics of species that coexist via this mechanism have not been extensively explored. Here, we examine both the nature of the dynamics and the responses of the mean densities of each predator to mortality im...

Predation at the microbial level can affect the fate of toxic trace metals. Metals associated with bacterial prey can be released into the dissolved phase following digestion by a predator, and/or metals can remain in the predator and be transferred potentially to the next level of the food chain. Toxic metal ions in the aqueous phase also are expected to modify the growth and predation rate of...

This paper considers the nonlinear observer normal forms and their application in an ecological Predator-Prey system. These forms allow for the design of robust observers for Predator-Prey models where full measurement is not available. Thus, from a measured population of one specie (prey or predator), one can estimate the population that is not directly measured.