A predator’s per capita feeding rate on prey, or its functional response, provides a foundation for predator–prey theory. Since 1959, Holling’s prey-dependent Type II functional response, a model that is a function of prey abundance only, has served as the basis for a large literature on predator–prey theory. We present statistical evidence from 19 predator–prey systems that three predator-depe...

Theoretical work on intraguild predation suggests that if a top predator and an intermediate predator share prey, the system will be stable only if the intermediate predator is better at exploiting the prey, and the top predator gains significantly from consuming the intermediate predator. In mammalian carnivore systems, however, there are examples of top predator species that attack intermedia...

the predator-prey model with stage structure for predator is generalized in the context of ecoepidemiology, where the prey population is infected by a microparasite and the predator completely avoids consuming the infected prey. the intraspecific competition of infected prey is considered. all the equilibria are characterized and the existence of a hopf bifurcation at the coexistence equilibriu...

Predator species identification is an important step in understanding predator-prey interactions, but predator identifications using kill site observations are often unreliable. We used molecular tools to analyse predator saliva, scat and hair from caribou calf kills in Newfoundland, Canada to identify the predator species, individual and sex. We sampled DNA from 32 carcasses using cotton swabs...

medicinal plants were used from past to present. different small arthropods such as acari were found on these plants. therefore a study on the acari fauna associated with some medicinal plants (family: asteraceae) in hamedan region was carried out during 2008–2009. in this survey, 23 species belonging 18 genera from 15 different families of the subclass acari were collected and identified. two ...

the present article deals with the inter specific competition and intra-specific competition among predator populations of a prey-dependent three component food chain model consisting of two competitive predator sharing one prey species as their food. the behaviour of the system near the biologically feasible equilibria is thoroughly analyzed. boundedness and dissipativeness of the system are e...

1. Interference between predator species frequently decreases predation rates, lowering the risk of predation for shared prey. However, such interference can also occur between conspecific predators. 2. Therefore, to understand the importance of predator biodiversity and the degree that predator species can be considered functionally interchangeable, we determined the degree of additivity and r...

Citation: Johnke J, Baron M, de Leeuw M, Kushmaro A, Jurkevitch E, Harms H and Chatzinotas A (2017) A Generalist Protist Predator Enables Coexistence in Multitrophic Predator-Prey Systems Containing a Phage and the Bacterial Predator Bdellovibrio. Front. Ecol. Evol. 5:124. doi: 10.3389/fevo.2017.00124 A Generalist Protist Predator Enables Coexistence in Multitrophic Predator-Prey Systems Contai...

In this survey, we briefly review some of our recent studies on predator-prey models with discrete delay. We first study the distribution of zeros of a second degree transcendental polynomial. Then we apply the general results on the distribution of zeros of the second degree transcendental polynomial to various predator-prey models with discrete delay, including Kolmogorov-type predator-prey m...