Dynamics in a diffusive predator–prey system with strong Allee effect and Ivlev-type functional response

The dynamics of a kind of reaction–diffusion predator–prey system with strong Allee effect in the prey population is considered. We prove the existence and uniqueness of the solution and give a priori bound. Hopf bifurcation and steady state bifurcation are studied. Results show that the Allee effect has significant impact on the dynamics.     

Dynamics of cooperative predator–prey system with impulsive effects and Beddington–DeAngelis functional response

In this paper, cooperative predator–prey system with impulsive effects and Beddington–DeAngelis functional response is studied. By using comparison theorem and some analysis techniques as well as the coincidence degree theory, sufficient conditions are obtained for the permanence, extinction and the existence of positive periodic solution.     

Global stability of a nonlinear stochastic predator–prey system with Beddington–DeAngelis functional response

Stochastically asymptotic stability in the large of a predator–prey system with Beddington–DeAngelis functional response with stochastic perturbation is considered. The result shows that if the positive equilibrium of the deterministic system is globally stable, then the stochastic model will preserve this nice property provided the noise is sufficiently small. Some simulation figures are introduced to support the analytical findings.     

Bifurcation analysis of a Leslie-type predator–prey system with simplified Holling type IV functional response and strong Allee effect on prey

In this paper, a Leslie-type predator–prey system with simplified Holling type IV functional response and strong Allee effect on prey is proposed. The dissipativity of the system and the existence of all possible equilibria are investigated. The investigation emphasizes the exploring of bifurcation. It is shown that the system exists several non-hyperbolic positive equilibria, such as a weak focus of multiplicities one and two, (degenerate) saddle–nodes and Bogdanov–Takens singularities (cusp case) of codimensions 2 and 3. At these equilibria, it is proved that the system undergoes various kinds of bifurcations, such as saddle–node bifurcation, Hopf bifurcation, degenerate Hopf bifurcation and Bogdanov–Takens bifurcation of codimensions 2 and 3. With the parameters selected properly, there exhibits a limit cycle, a homoclinic loop, two limit cycles, a semistable limit cycle, or the simultaneous occurrence of a homoclinic loop and a limit cycle in the system. Moreover, it is also proved that the system has a cusp of codimension at least 4. Hence, there may exist three limit cycles generated from Hopf bifurcation of codimension 3. Numerical simulations are done to support the theoretical results.     

Dynamics of impulsive reaction–diffusion predator–prey system with Holling type III functional response

An impulsive reaction–diffusion periodic predator–prey system with Holling type III functional response is investigated in the present paper. Sufficient conditions for the ultimate boundedness and permanence of the predator–prey system are established based on the upper and lower solution method and comparison theory of differential equation. By constructing an appropriate auxiliary function, the conditions for the existence of a unique globally stable positive periodic solution are also obtained. Some numerical examples are presented to verify our results. A discussion is given at the end.     

Dynamics of a reaction–diffusion–ODE system with quiescence

We consider a reaction–diffusion–ODE quiescent model in which the species can switch between mobile and immobile categories. We assume that the population inhabits a bounded region and study how its dynamics depend on the parameters describing switching rates and local population dynamics. Our results suggest that the transfer displays a stabilizing effect and inhibits the generation of spatial periodic solutions. A new method to obtain global stability and dissipative structure is also explored by constructing Lyapunov functionals to overcome the loss of compactness.     

Stability of the virus dynamics model with Beddington–DeAngelis functional response and delays

A virus dynamics model with Beddington–DeAngelis functional response and delays is introduced. By analyzing the characteristic equations, the local stability of an infection-free equilibrium and a chronic-infection equilibrium of the model is established. By using suitable Lyapunov functionals and the LaSalle invariance principle, we show that the infection-free equilibrium is globally asymptotically stable if _R0?1$R_0?1$ and the chronic-infection equilibrium is globally asymptotically stable if _R0>1$R_0>1$. Numerical simulations are also given to explain our results.     

Global stability of stage-structured predator–prey models with Beddington–DeAngelis functional response

Two stage-structured predator–prey systems with Beddington–DeAngelis functional response are proposed. The first one is deterministic. The Second one takes the random perturbation into account. For each system, sufficient conditions for global asymptotic stability are established. Some simulation figures are introduced to support the analytical findings.     

Global properties for virus dynamics model with Beddington–DeAngelis functional response

This paper investigates the global stability of virus dynamics model with Beddington–DeAngelis infection rate. By constructing Lyapunov functions, the global properties have been analysed. If the basic reproductive ratio of the virus is less than or equal to one, the uninfected steady state is globally asymptotically stable. If the basic reproductive ratio of the virus is more than one, the infected steady state is globally asymptotically stable. The conditions imply that the steady states are always globally asymptotically stable for Holling type II functional response or for a saturation response.     

The impact of Allee effect on a predator–prey system with Holling type II functional response

In this paper, the Allee effect is incorporated into a predator–prey model with Holling type II functional response. Compared with the predator–prey model without Allee effect, we find that the Allee effect of prey species increases the extinction risk of both predators and prey. When the handling time of predators is relatively short and the Allee effect of prey species becomes strong, both predators and prey may become extinct. Moreover, it is shown that the model with Allee effect undergoes the Hopf bifurcation and heteroclinic bifurcation. The Allee effect of prey species can lead to unstable periodical oscillation. It is also found that the positive equilibrium of the model could change from stable to unstable, and then to stable when the strength of Allee effect or the handling time of predators increases continuously from zero, that is, the model admits stability switches as a parameter changes. When the Allee effect of prey species becomes strong, longer handling time of predators may stabilize the coexistent steady state.     

Steady state in a cross-diffusion predator–prey model with the Beddington–DeAngelis functional response

The purpose of this paper is to study the existence of steady state in a linear cross-diffusion predator–prey model with Beddington–DeAngelis functional response. The proofs mainly rely on Fixed point index theory and analytical techniques.     

Asymptotic behavior of reaction–advection–diffusion population models with Allee effect

In this work, a qualitative analysis is carried out for reaction–advection–diffusion (RAD) systems modeling the interactions between two species with Allee effect. In particular, we study different scenarios: mutualism, competition, and a predator–prey relationship in order to investigate the survival or extinction of both populations. Global existence and uniqueness of positive solutions of the proposed RAD problems are demonstrated. Equilibrium states and asymptotic behavior of solutions are obtained using the monotone method and the upper and lower solutions technique. Numerical simulations by a Crank–Nicolson monotone iterative method of the different asymptotic solution dynamics are shown to illustrate our theoretical results.     

Dynamics of predator–prey models with a strong Allee effect on the prey and predator-dependent trophic functions

The complex dynamics of a two-trophic chain are investigated. The chain is described by a general predator–prey system, in which the prey growth rate and the trophic interaction functions are defined only by some properties determining their shapes. To account for undercrowding phenomena, the prey growth function is assumed to model a strong Allee effect; to simulate the predator interference during the predation process, the trophic function is assumed predator-dependent. A stability analysis of the system is performed, using the predation efficiency and a measure of the predator interference as bifurcation parameters. The admissible scenarios are much richer than in the case of prey-dependent trophic functions, investigated in Buffoni et al. (2011). General conditions for the number of equilibria, for the existence and stability of extinction and coexistence equilibrium states are determined, and the bifurcations exhibited by the system are investigated. Numerical results illustrate the qualitative behaviours of the system, in particular the presence of limit cycles, of global bifurcations and of bistability situations.     

Permanence and periodic solutions for an impulsive reaction–diffusion food-chain system with ratio-dependent functional response

An impulsive reaction–diffusion periodic food-chain system with ratio-dependent functional response is investigated in the present paper. Sufficient conditions for the ultimate boundedness and permanence of the food-chain system are established based on the comparison theory of differential equation and upper and lower solution method. By constructing appropriate auxiliary function, the conditions for the existence of a unique globally stable positive periodic solution are also obtained. Some numerical examples are presented to verify our results. A discussion is given in the end of the paper.