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.     

Stochastic persistence and stability analysis of a modified Holling–Tanner model

The article aims to study the basic dynamical features of a modified Holling–Tanner prey–predator model with ratio‐dependent functional response. We have proved the global existence of the solution for the deterministic model. The parametric restriction for persistence of both species is also obtained along with the proof of local asymptotic stability of the interior equilibrium point(s). Conditions for local bifurcations of interior equilibrium points are provided. The global dynamic behavior is examined thoroughly with supportive numerical simulation results. Next, we have formulated the stochastic model by perturbing the intrinsic growth rates of prey and predator populations with white noise terms. The existence uniqueness of solutions for stochastic model is established. Further, we have derived the parametric restrictions required for the persistence of the stochastic model. Finally, we have discussed the stochastic stability results in terms of the first and second order moments. Numerical simulation results are provided to support the analytical findings. Copyright © 2012 John Wiley & Sons, Ltd.     

Global bifurcation of solutions for a predator–prey model with prey‐taxis

We study pattern formations in a predator–prey model with prey‐taxis. It is proved that a branch of nonconstant solutions can bifurcate from the positive equilibrium only when the chemotactic is repulsive. Furthermore, we find the stable bifurcating solutions near the bifurcation point under suitable conditions. Copyright © 2014 John Wiley & Sons, Ltd.     

On a stochastic predator‐prey system with modified functional response

A stochastic predator–prey system with modified functional response is investigated. We show that there is a unique positive solution to the model for any positive initial value by comparison theorem. Moreover, under some conditions, we conclude that the stochastic model is persistent in mean and extinct. Copyright © 2011 John Wiley & Sons, Ltd.     

Consequences of weak Allee effect on prey in the May–Holling–Tanner predator–prey model

In this work, a modified Holling–Tanner predator–prey model is analyzed, considering important aspects describing the interaction such as the predator growth function is of a logistic type; a weak Allee effect acting in the prey growth function, and the functional response is of hyperbolic type. Making a change of variables and time rescaling, we obtain a polynomial differential equations system topologically equivalent to the original one in which the non‐hyperbolic equilibrium point (0,0) is an attractor for all parameter values. An important consequence of this property is the existence of a separatrix curve dividing the behavior of trajectories in the phase plane, and the system exhibits the bistability phenomenon, because the trajectories can have different ω ? limit sets; as example, the origin (0,0) or a stable limit cycle surrounding an unstable positive equilibrium point. We show that, under certain parameter conditions, a positive equilibrium may undergo saddle‐node, Hopf, and Bogdanov–Takens bifurcations; the existence of a homoclinic curve on the phase plane is also proved, which breaks in an unstable limit cycle. Some simulations to reinforce our results are also shown. Copyright © 2015 John Wiley & Sons, Ltd.     

Consequences of refuge and diffusion in a spatiotemporal predator–prey model

In this investigation, we offer and examine a predator–prey interacting model with prey refuge in proportion to both the species and Beddington–DeAngelis functional response. We first prove the well-posedness of the temporal and spatiotemporal models which are restricted in a positive invariant region. Then for the temporal model, we analyse its temporal dynamics including uniform boundedness, permanence, stability of all feasible non-negative equilibria and show that refugia can induce periodic oscillation via Hopf bifurcation around the unique positive equilibrium; for the spatiotemporal model, we not only investigate its permanence, stability of non-negative constant steady states and Turing instability but also study the existence and non-existence of non-constant positive steady states by Leray–Schauder degree theory. The key observation is that the coefficient of refuge cooperates a significant part in modifying the dynamics of the current system and mediates the population permanence, stability of coexisting equilibrium and even the Turing instability parameter space. Finally, general numerical simulation consequences are given to illustrate the validity of the theoretical results. Through numerical simulations, one observes that the model dynamics shows prey refugia and self-diffusion control spatiotemporal pattern growth to spots, stripe–spot mixtures and stripes reproduction. The outcomes assign that the dynamics of the model with prey refuge is not simple, but rich and complex. Additionally, numerical simulations show that the other model parameters have an important effect on species’ spatially inhomogeneous distribution, which results in the formation of spots pattern, mixture of spots and stripes pattern, mixture of spots, stripes and rings pattern and anti-spot pattern. This may improve the model dynamics of the prey refuge on the reaction–diffusion predator–prey system.     

Stability analysis of an epidemic model with diffusion and stochastic perturbation

In this paper, we investigate the stability of an epidemic model with diffusion and stochastic perturbation. We first show both the local and global stability of the endemic equilibrium of the deterministic epidemic model by analyzing corresponding characteristic equation and Lyapunov function. Second, for the corresponding reaction–diffusion epidemic model, we present the conditions of the globally asymptotical stability of the endemic equilibrium. And we carry out the analytical study for the stochastic model in details and find out the conditions for asymptotic stability of the endemic equilibrium in the mean sense. Furthermore, we perform a series of numerical simulations to illustrate our mathematical findings.     

Classical predator–prey system with infection of prey population—a mathematical model

The present paper deals with the problem of a classical predator–prey system with infection of prey population. A classical predator–prey system is split into three groups, namely susceptible prey, infected prey and predator. The relative removal rate of the susceptible prey due to infection is worked out. We observe the dynamical behaviour of this system around each of the equilibria and point out the exchange of stability. It is shown that local asymptotic stability of the system around the positive interior equilibrium ensures its global asymptotic stability. We prove that there is always a Hopf bifurcation for increasing transmission rate. To substantiate the analytical findings, numerical experiments have been carried out for hypothetical set of parameter values. Our analysis shows that there is a threshold level of infection below which all the three species will persist and above which the disease will be epidemic. Copyright © 2003 John Wiley & Sons, Ltd.     

Limit cycles in a Gause‐type predator–prey model with sigmoid functional response and weak Allee effect on prey

The goal of this work is to examine the global behavior of a Gause‐type predator–prey model in which two aspects have been taken into account: (i) the functional response is Holling type III; and (ii) the prey growth is affected by a weak Allee effect. Here, it is proved that the origin of the system is a saddle point and the existence of two limit cycles surround a stable positive equilibrium point: the innermost unstable and the outermost stable, just like with the strong Allee effect. Then, for determined parameter constraints, the trajectories can have different ω ? limit sets. The coexistence of a stable limit cycle and a stable positive equilibrium point is an important fact for ecologists to be aware of the kind of bistability shown here. So, these models are undoubtedly rather sensitive to disturbances and require careful management in applied contexts of conservation and fisheries. Copyright © 2012 John Wiley & Sons, Ltd.     

Bogdanov–Takens bifurcation in a predator–prey model

In this paper, we investigate a class of predator–prey model with age structure and discuss whether the model can undergo Bogdanov–Takens bifurcation. The analysis is based on the normal form theory and the center manifold theory for semilinear equations with non-dense domain combined with integrated semigroup theory. Qualitative analysis indicates that there exist some parameter values such that this predator–prey model has an unique positive equilibrium which is Bogdanov–Takens singularity. Moreover, it is shown that under suitable small perturbation, the system undergoes the Bogdanov–Takens bifurcation in a small neighborhood of this positive equilibrium.     

Qualitative analysis of Holling type II predator–prey systems with prey refuges and predator restricts

This paper is devoted to investigation of Holling type II predator–prey systems with prey refuges and predator restricts. Using a transformation technique, we change the system into a generalized Liénard system and give sufficient conditions to ensure the global stability of the positive equilibrium and existence and uniqueness of a stable limit cycle. We also find the property of alternation for phase structure of the system.     

Stochastic analysis of prey-predator model with stage structure for prey

The present paper deals with the effect of environmental fluctuation on a prey-predator model with stage structure for prey population. We have studied the stochastic behaviour of the model system around coexisting equilibrium point. Stochastic stability condition in mean square sense is obtained for the stage-structured model with help of a suitable Lyapunov function. Numerical simulations are carried out to substantiate the analytical findings. The main outcomes of mathematical findings are mentioned in conclusion section.     

A modified Leslie–Gower predator–prey model with ratio‐dependent functional response and alternative food for the predator

In this work, a modified Leslie–Gower predator–prey model is analyzed, considering an alternative food for the predator and a ratio‐dependent functional response to express the species interaction. The system is well defined in the entire first quadrant except at the origin ( 0 , 0 ) . Given the importance of the origin ( 0 , 0 ) as it represents the extinction of both populations, it is convenient to provide a continuous extension of the system to the origin. By changing variables and a time rescaling, we obtain a polynomial differential equations system, which is topologically equivalent to the original one, obtaining that the non‐hyperbolic equilibrium point ( 0 , 0 ) in the new system is a repellor for all parameter values. Therefore, our novel model presents a remarkable difference with other models using ratio‐dependent functional response. We establish conditions on the parameter values for the existence of up to two positive equilibrium points; when this happen, one of them is always a hyperbolic saddle point, and the other can be either an attractor or a repellor surrounded by at least one limit cycle. We also show the existence of a separatrix curve dividing the behavior of the trajectories in the phase plane. Moreover, we establish parameter sets for which a homoclinic curve exits, and we show the existence of saddle‐node bifurcation, Hopf bifurcation, Bogdanov–Takens bifurcation, and homoclinic bifurcation. An important feature in this model is that the prey population can go to extinction; meanwhile, population of predators can survive because of the consumption of alternative food in the absence of prey. In addition, the prey population can attain their carrying capacity level when predators go to extinction. We demonstrate that the solutions are non‐negatives and bounded (dissipativity and permanence of population in many other works). Furthermore, some simulations to reinforce our mathematical results are shown, and we further discuss their ecological meanings. Copyright © 2017 John Wiley & Sons, Ltd.     

Asymptotic stability of one prey and two predators model with two functional responses

We formulate a mathematical model to study the complex dynamical behavior of a three dimensional model consisting of one prey and two predators involving Beddington–DeAngelis and Crowley–Martin functional responses. The existence and stability conditions of the equilibrium points are analyzed. The global asymptotic stability of the interior equilibrium point, if exists, is proved by considering Lyapunov function. Several numerical simulations are performed to illustrate the theoretical analysis. The multiple states of stability are observed in one example whereas another example exhibits the global stability of interior equilibrium point.

     

A predator–prey model with disease in the prey species only

A predator–prey model with transmissible disease in the prey species is proposed and analysed. The essential mathematical features are analysed with the help of equilibrium, local and global stability analyses and bifurcation theory. We find four possible equilibria. One is where the populations are extinct. Another is where the disease and predator populations are extinct and we find conditions for global stability of this. A third is where both types of prey exist but no predators. The fourth has all three types of individuals present and we find conditions for limit cycles to arise by Hopf bifurcation. Experimental data simulation and brief discussion conclude the paper. Copyright © 2006 John Wiley & Sons, Ltd.     

Global stability of the equilibrium of a diffusive Holling–Tanner prey–predator model

This work is concerned with a Holling–Tanner prey–predator model with diffusion subject to the homogeneous Neumann boundary condition. We will obtain some results for the global stability of the unique positive equilibrium of this model, and thus improve some previous results.     

Multiple stability and uniqueness of the limit cycle in a Gause-type predator–prey model considering the Allee effect on prey

In this work, a bidimensional differential equation system obtained by modifying the well-known predator–prey Rosenzweig–MacArthur model is analyzed by considering prey growth influenced by the Allee effect.One of the main consequences of this modification is a separatrix curve that appears in the phase plane, dividing the behavior of the trajectories. The results show that the equilibrium in the origin is an attractor for any set of parameters. The unique positive equilibrium, when it exists, can be either an attractor or a repeller surrounded by a limit cycle, whose uniqueness is established by calculating the Lyapunov quantities. Therefore, both populations could either reach deterministic extinction or long-term deterministic coexistence.The existence of a heteroclinic curve is also proved. When this curve is broken by changing parameter values, then the origin turns out to be an attractor for all orbits in the phase plane. This implies that there are plausible conditions where both populations can go to extinction. We conclude that strong and weak Allee effects on prey population exert similar influences on the predator–prey model, thereby increasing the risk of ecological extinction.     

On the dimension of the subspace of Liouvillian solutions of a Fuchsian system

The effect of small constantly acting random perturbations of white noise type on a dynamical system with locally stable fixed point is studied. The perturbed system is considered in the form of Itô stochastic differential equations, and it is assumed that the perturbation does not vanish at a fixed point. In this case, the trajectories of the stochastic system issuing from points near the stable fixed point exit from the neighborhood of equilibrium with probability 1. Classes of perturbations such that the equilibrium of a deterministic system is stable in probability on an asymptotically large time interval are described.     

Stability,Steady‐State Bifurcations,and Turing Patterns in a Predator–Prey Model with Herd Behavior and Prey‐taxis

In this paper, we consider a predator–prey model with herd behavior and prey‐taxis subject to the homogeneous Neumann boundary condition. First, by analyzing the characteristic equation, the local stability of the positive equilibrium is discussed. Then, choosing prey‐tactic sensitivity coefficient as the bifurcation parameter, we obtain a branch of nonconstant solutions bifurcating from the positive equilibrium by an abstract bifurcation theory, and find the stable bifurcating solutions near the bifurcation point under suitable conditions. We have shown that prey‐taxis can destabilize the uniform equilibrium and yields the occurrence of spatial patterns. Furthermore, some numerical simulations to illustrate the theoretical analysis are also carried out, Turing patterns such as spots pattern, spots–strip pattern, strip pattern, stable nonconstant steady‐state solutions, and spatially inhomogeneous periodic solutions are obtained, which also expand our theoretical results.     

On global asymptotic stability of the equilibrium of “predator–prey” system in varying environment

This paper considers a predator–prey system of differential equations. This ecological system is a model of Lotka–Volterra type whose prey population receives time-variation of the environment. It is not assumed that the time-varying coefficient is weakly integrally positive. We obtain sufficient conditions of global asymptotic stability of the unique interior equilibrium if the time-variation is bounded.