Effect of prey-taxis on predator’s invasion in a spatially heterogeneous environment

In this study, we consider a diffusive predator–prey system with prey-taxis and ratio-dependent functional responses in a spatially heterogeneous environment. Prey-taxis implies that the predator exhibits directed movement in the presence of prey. We claim that when the predator diffuses uniformly without prey-taxis, only the diffusion of the species plays a role in the predator’s invasion in a spatially homogeneous environment. However, when the predator disperses through uniform diffusion together with prey-taxis, we observe that both the diffusion of species and prey-taxis affect the invasion of the predator, which is not the case in a spatially homogeneous environment. The results are obtained by investigating the local stability of a semi-trivial solution, using an eigenvalue analysis.     

Analysis of a prey-predator model with disease in prey

In this paper, a system of reaction-diffusion equations arising in eco-epidemiological systems is investigated. The equations model a situation in which a predator species and a prey species inhabit the same bounded region and the predator only eats the prey with transmissible diseases. A number of existence and non-existence results about the non-constant steady states of a reaction diffusion system are given. It is proved that if the diffusion coefficient of the predator is treated as bifurcation parameter, non-constant positive steady-state solutions may bifurcate from the constant steady-state solution under some conditions.     

Turing pattern formation in a three species model with generalist predator and cross-diffusion

In a natural ecosystem, specialist predators feed almost exclusively on one species of prey. But generalist predators feed on many types of species. Consequently, their dynamics is not coupled to the dynamics of a specific prey population. However, the defense of prey formed by congregating made the predator tend to move in the direction of lower concentration of prey species. This is described by cross-diffusion in a generalist predator–prey model. First, the positive equilibrium solution is globally asymptotically stable for the ODE system and for the reaction–diffusion system without cross-diffusion, respectively, hence it does not belong to the classical Turing instability scheme. But it becomes linearly unstable only when cross-diffusion also plays a role. This implies that cross–diffusion can lead to the occurrence and disappearance of the instability. Our results exhibit some interesting combining effects of cross-diffusion, predations and intra-species interactions. Furthermore, we consider the existence and non-existence results concerning non-constant positive steady states (patterns) of the system. We demonstrate that cross-diffusion can create non-constant positive steady-state solutions.     

Dynamics and pattern formations in diffusive predator‐prey models with two prey‐taxis

A reaction‐diffusion two‐predator‐one‐prey system with prey‐taxis describes the spatial interaction and random movement of predator and prey species, as well as the spatial movement of predators pursuing preys. The global existence and boundedness of solutions of the system in bounded domains of arbitrary spatial dimension and any small prey‐taxis sensitivity coefficient are investigated by the semigroup theory. The spatial pattern formation induced by the prey‐taxis is characterized by the Turing type linear instability of homogeneous state; it is shown that prey‐taxis can both compress and prompt the spatial patterns produced through diffusion‐induced instability in two‐predator‐one‐prey systems.     

Analysis of a Prey-predator Model with Disease in Prey

In this paper, a system of reaction-diffusion equations arising in ecoepidemiological systems is investigated. The equations model a situation in which a predator species and a prey species inhabit the same bounded region and the predator only eats the prey with transmissible diseases. Local stability of the constant positive solution is considered. A number of existence and non-existence results about the nonconstant steady states of a reaction diffusion system are given. It is proved that if the diffusion coefficient of the prey with disease is treated as a bifurcation parameter, non-constant positive steady-state solutions may bifurcate from the constant steadystate solution under some conditions.     

Waves analysis and spatiotemporal pattern formation of an ecosystem model

In this paper, we consider a predator–prey model given by a reaction–diffusion system. This model incorporates Holling-type-II (Michaelis–Menten) and modified Leslie-Gower functional responses. We show the existence of qualitatively different types of system behaviors realized for various parameter values. Our model is investigated with methods of the qualitative theory and the theory of bifurcations. We generalize the traveling waves existence method for populations dynamics with positive derivative densities, to the predator–prey system in which growth densities may change sign. Parallel to this is a discussion and an analysis of alternative model outcomes such as complex pattern formation and spatio-temporal chaos behavior.     

Spatial patterns of the Holling–Tanner predator–prey model with nonlinear diffusion effects

In this article, we study the Holling–Tanner predator–prey model with nonlinear diffusion terms under homogeneous Neumann boundary condition. The nonlinear diffusion terms here mean that the prey runs away from the predator, and the predator chases the prey. Nonexistence and existence of nonconstant positive steady states are obtained, which reveal that cross-diffusion can create spatial patterns even when the random diffusion fails to do so. Moreover, asymptotic behaviour of positive solutions as the cross-diffusion tends to ∞ is shown.     

A predator–prey system with stage-structure for predator and nonlocal delay

This paper deals with the behavior of solutions to the reaction–diffusion system under homogeneous Neumann boundary condition, which describes a prey–predator model with nonlocal delay. Sufficient conditions for the global stability of each equilibrium are derived by the Lyapunov functional and the results show that the introduction of stage-structure into predator positively affects the coexistence of prey and predator. Numerical simulations are performed to illustrate the results.     

Existence and non‐existence of steady states to a cross‐diffusion system arising in a Leslie predator–prey model

This paper is concerned with a cross‐diffusion system arising in a Leslie predator–prey population model in a bounded domain with no flux boundary condition. We investigate sufficient condition for the existence and the non‐existence of non‐constant positive solution. We obtain that if natural diffusion coefficient of predator is large enough and cross‐diffusion coefficients are fixed, then under some conditions there exists non‐constant positive solution. Furthermore, we show that if natural diffusion coefficients of predator and prey are both large enough, and cross‐diffusion coefficients are small enough, then there exists no non‐constant positive solution. Copyright © 2012 John Wiley & Sons, Ltd.     

Predator invasion in predator–prey model with prey-taxis in spatially heterogeneous environment

We consider a predator–prey model with prey-taxis and Holling-type II functional responses in a spatially heterogeneous environment to analyze the effects of prey-taxis and the heterogeneity of an environment on predator invasion. To achieve our goal, we investigate the stability of semi-trivial solution in which the predator is absent. It is known that both the predator diffusion and the death rate contribute to the predator invasion in a heterogeneous habitat when there is no prey-taxis. In this paper, we show that predator invasion is affected by the prey-taxis and diffusions of the prey-taxis model for a certain range of predator death rates in a heterogeneous environment. Furthermore, in cases where predator invasion by predator diffusion does not occur in a particular death rate range of the predator, predator invasion can occur by prey-taxis in a spatially heterogeneous habitat. In addition, we compare this phenomenon to the corresponding predator–prey model with ratio-dependent functional responses. It is observed that none of the predator’s diffusion and prey-taxis affect the predator’s invasion, and that only the predator’s death rate contributes to predator invasion for the model with ratio-dependent functional responses.     

Global existence in a food chain model consisting of two competitive preys,one predator and chemotaxis

A model for the spatio-temporal evolution of three biological species in a food chain model consisting of two competitive preys and one predator with intra-specific competition is considered. Besides diffusing, the predator species moves toward higher concentrations of a chemical substance produced by the prey. The prey, in turn, moves away from high concentrations of a substance secreted by the predators. The resulting reaction–diffusion system consists of three parabolic equations along with three elliptic equations describing the diffusion of the chemical substances. The local existence of nonnegative solutions is proved. Then uniform estimates in Lebesgue spaces are provided. These estimates lead to boundedness and global well-posedness for the system. Numerical simulations are presented and discussed.     

On a nonlinear nonautonomous predator–prey model with diffusion and distributed delay

In this paper, a nonlinear nonautonomous predator–prey model with diffusion and continuous distributed delay is studied, where all the parameters are time-dependent. The system, which is composed of two patches, has two species: the prey can diffuse between two patches, but the predator is confined to one patch. We first discuss the uniform persistence and global asymptotic stability of the model; after that, by constructing a suitable Lyapunov functional, some sufficient conditions for the existence of a unique almost periodic solution of the system are obtained. An example shows the feasibility of our main results.     

Investigating the Turing Conditions for Diffusion-driven Instability in Predator-prey System with Hunting Cooperation Functional Response

In this paper, we focus on stability analysis of steady-state solutions of a predator-prey system with hunting cooperation functional response. The results show that the Turing instability can be affected not only the existence of hunting cooperation, but also the diffusion coefficients: (1) in the absence of predator diffusion, diffusion-driven instability can be induced by hunting cooperation, but no stable patterns appear; (2) the system can occur diffusion-driven instability and Turing patterns, when both predator and prey have diffusion, and the diffusion coefficient of prey is greater than that of the predator. The numerical simulations of two cases are presented to verify the validity of our theoretical results.     

Stability and Hopf bifurcation of a diffusive predator‐prey model with hyperbolic mortality

The dynamics of a reaction‐diffusion predator‐prey model with hyperbolic mortality and Holling type II response effect is considered. The stability of the positive equilibrium and the existence of Hopf bifurcation are investigated by analyzing the distribution of eigenvalues without diffusion. We also study the spatially homogeneous and nonhomogeneous periodic solutions through all parameters of the system which are spatially homogeneous. To verify our theoretical results, some numerical simulations are also presented. © 2015 Wiley Periodicals, Inc. Complexity 21: 34–43, 2016     

Two-patches prey impulsive diffusion periodic predator–prey model

In this paper, we study a periodic predator–prey system with prey impulsive diffusion in two patches. On the basis of comparison theorem of impulsive differential equation and other analysis methods, sufficient and necessary conditions on the predator–prey system where predator have not other food source are established. Two examples and numerical simulations are presented to illustrate the feasibility of our results. A conclusion is given in the end.     

Nonconstant Positive Steady States and Pattern Formation of 1D Prey-Taxis Systems

Prey-taxis is the process that predators move preferentially toward patches with highest density of prey. It is well known to have an important role in biological control and the maintenance of biodiversity. To model the coexistence and spatial distributions of predator and prey species, this paper concerns nonconstant positive steady states of a wide class of prey-taxis systems with general functional responses over 1D domain. Linearized stability of the positive equilibrium is analyzed to show that prey-taxis destabilizes prey–predator homogeneity when prey repulsion (e.g., due to volume-filling effect in predator species or group defense in prey species) is present, and prey-taxis stabilizes the homogeneity otherwise. Then, we investigate the existence and stability of nonconstant positive steady states to the system through rigorous bifurcation analysis. Moreover, we provide detailed and thorough calculations to determine properties such as pitchfork and turning direction of the local branches. Our stability results also provide a stable wave mode selection mechanism for thee reaction–advection–diffusion systems including prey-taxis models considered in this paper. Finally, we provide numerical studies of prey-taxis systems with Holling–Tanner kinetics to illustrate and support our theoretical findings. Our numerical simulations demonstrate that the \(2\times 2\) prey-taxis system is able to model the formation and evolution of various striking patterns, such as spikes, periodic oscillations, and coarsening even when the domain is one-dimensional. These dynamics can model the coexistence and spatial distributions of interacting prey and predator species. We also give some insights on how system parameters influence pattern formation in these models.     

Coexistence steady states in a predator–prey model

An age-structured predator–prey system with diffusion and Holling–Tanner-type nonlinearities is investigated. Regarding the intensity of the fertility of the predator as bifurcation parameter, we prove that a branch of positive coexistence steady states bifurcates from the marginal steady state with no predator. A similar result is shown when the fertility of the prey varies.     

A bioeconomic differential algebraic predator–prey model with nonlinear prey harvesting

In this paper, we propose a bioeconomic differential algebraic predator–prey model with Holling type II functional response and nonlinear prey harvesting. As the nonlinear prey harvesting is introduced, the proposed model displays a complex dynamics in the predator–prey plane. Taking into account of the economic factor, our predator–prey system is established by bioeconomic differential algebraic equations. The effect of economic profit on the proposed model is analyzed by viewing it as a bifurcation parameter. By jointly using the normal form of differential algebraic models and the bifurcation theory, the stability and bifurcations (singularity induced bifurcation, Hopf bifurcation) are discussed. These results obtained here reveal richer dynamics of the bioeconomic differential algebraic predator–prey model with nonlinear prey harvesting, and suggest a guidance for harvesting in the practical word. Finally, numerical simulations are given to demonstrate the results.     

Traveling waves in delayed predator–prey systems with nonlocal diffusion and stage structure

This paper is concerned with the existence of traveling wave solutions of a delayed predator–prey system with stage structure and nonlocal diffusion. By introducing the partial quasi-monotone condition and cross-iteration scheme, we first consider a class of delayed systems with nonlocal diffusion and deduce the existence of traveling wave solutions to the existence of a pair of upper–lower solutions. When the result is applied to the predator–prey system, we establish the existence of traveling wave solutions, as well as its precisely asymptotic behavior. Our result implies that there is a transition zone moving from the steady state with no species to the steady state with the coexistence of both species.