Foraging movements of predator play an important role in population dynamics of prey-predator interactions, which have been considered as mechanisms that contribute to spatial self-organization of prey and predator. In nature, there are many examples of prey-predator interactions where prey is immobile while predator disperses between patches non-randomly through different factors such as stimu...

Simple rules based on population equilibria can characterize indirect interactions in threespecies systems but fail to predict them when considering behavioral mechanisms. In this paper, we revisit the effects of shared predation, i.e. the situation in which two prey are consumed by a common predator. Such predation usually induces negative indirect interactions between prey, or apparent compet...

Intraguild predation (IGP) is a combination of competition and predation which is the most basic system in food webs that contains three species where two species that are involved in a predator/prey relationship are also competing for a shared resource or prey. We formulate two intraguild predation (IGP: resource, IG prey and IG predator) models: one has generalist predator while the other one...

A long-standing debate concerns how functional responses are best described. Theory suggests that ratio dependence is consistent with many food web patterns left unexplained by the simplest prey-dependent models. However, for logistical reasons, ratio dependence and predator dependence more generally have seen infrequent empirical evaluation and then only so in specialist predators, which are r...

Predator-prey body mass relationships are a vital part of food webs across ecosystems and provide key information for predicting the susceptibility of carnivore populations to extinction. Despite this, there has been limited research on the minimum and maximum prey size of mammalian carnivores. Without information on large-scale patterns of prey mass, we limit our understanding of predation pre...

Predator-prey models with Hassell-Varley type functional response are appropriate for interactions where predators form groups and have applications in biological control. Here we present a systematic global qualitative analysis to a general predator-prey model with Hassell-Varley type functional response. We show that the predator free equilibrium is a global attractor only when the predator d...

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...

predation rate is basic to any investigation of prey-predator interaction and a major component in the selection of predators for biological control. the predation rate of variegated lady beetle, hippodamia variegata (goze), fed on different densities (20, 40, 60, 80 and 100) of third instar nymphs of cotton aphid, aphis gossypii glover, was studied under laboratory conditions (25 ± 1 °c, 65 ± ...

Theoretical models of predator-prey systems predict that sufficient enrichment of prey can generate large amplitude limit cycles, paradoxically causing a high risk of extinction (the paradox of enrichment). Although real ecological communities contain many gregarious species, whose foraging behaviour should be influenced by socially transmitted information, few theoretical studies have examined...

The dynamics of the planar two-species Lotka-Volterra predator-prey model are well-understood. Onto such a predator-prey model, we introduce a third species, a scavenger of the prey. Our model allows for two scenarios, one where the scavenger is also a predator of the original prey, and one where the presence of the scavenger simply inhibits the prey. We show all trajectories are bounded in for...