Positive Solutions for a Lotka–Volterra Prey–Predator Model with Cross-Diffusion of Fractional Type

In this paper we consider a Lotka–Volterra prey–predator model with cross-diffusion of fractional type. The main purpose is to discuss the existence and nonexistence of positive steady state solutions of such a model. Here a positive solution corresponds to a coexistence state of the model. Firstly we study the stability of the trivial and semi-trivial solutions by analyzing the principal eigenvalue of the corresponding linearized system. Secondly we derive some necessary conditions to ensure the existence of positive solutions, which demonstrate that if the intrinsic growth rate of the prey is too small or the death rate (or the birth rate) of the predator is too large, the model does not possess positive solutions. Thirdly we study the sufficient conditions to ensure the existence of positive solutions by using degree theory. Finally we characterize the stable/unstable regions of semi-trivial solutions and coexistence regions in parameter plane.     

On a Predator–Prey System with Digestion Delay and Anti-predation Strategy

Journal of Nonlinear Science - Predator–prey interactions are among the most complicated interactions between biological species, in which there may be both direct effect (through predation)...     

Asymptotic Behavior of Solutions in One Predator–Prey Model with Delay

Siberian Mathematical Journal - We consider some system of delay differential equations describing the interaction between predator and prey populations and accounting for the age structure of the...     

Dynamics of a Stochastic Predator–Prey Model with Stage Structure for Predator and Holling Type II Functional Response

In this paper, we develop and study a stochastic predator–prey model with stage structure for predator and Holling type II functional response. First of all, by constructing a suitable stochastic Lyapunov function, we establish sufficient conditions for the existence and uniqueness of an ergodic stationary distribution of the positive solutions to the model. Then, we obtain sufficient conditions for extinction of the predator populations in two cases, that is, the first case is that the prey population survival and the predator populations extinction; the second case is that all the prey and predator populations extinction. The existence of a stationary distribution implies stochastic weak stability. Numerical simulations are carried out to demonstrate the analytical results.     

Bifurcations in a Diffusive Predator–Prey Model with Beddington–DeAngelis Functional Response and Nonselective Harvesting

In this paper, we discuss the dynamics of a predator–prey model with Beddington–DeAngelis functional response and nonselective harvesting. By using the Lyapunov–Schmidt reduction, we obtain the existence of spatially nonhomogeneous steady-state solution. The stability and existence of Hopf bifurcation at the spatially nonhomogeneous steady-state solution with the change of a specific parameter are investigated by analyzing the distribution of the eigenvalues. We also get an algorithm for determining the bifurcation direction of the Hopf bifurcating periodic solutions near the nonhomogeneous steady-state solution. Finally, we show some numerical simulations to verify our analytical results.

     

Complex Dynamics of an Impulsive Control System in which Predator Species Share a Common Prey

In an ecosystem, multiple predator species often share a common prey and the interactions between the predators are neutral. In view of this fact, we propose a three-species prey-predator system with the functional responses and impulsive controls to model the process of pest management. It is proved that the system has a locally stable pest-eradication periodic solution under the assumption that the impulsive period is less than some critical value. In particular, two single control strategies (biological control alone or chemical control alone) are proposed. Finally, we compare three pest control strategies and find that if we choose narrow-spectrum pesticides that are targeted to a specific pest’s life cycle to kill the pest, then the combined strategy is preferable. Numerical results show that our system has complex dynamics including period-doubling bifurcation, quasi-periodic oscillation, chaos, intermittency and crises. This work is supported by National Natural Science Foundation of China (10171106).     

Global Stability for a Generalized Predator—Prey System with Time Delay In Two-patch Environments

In this article the asymptotic behavior of solutions of a predator—prey system is investigated. The model incorporates time delay due to gestation and assumes that the prey disperses between two patches of a heterogeneous environment with barriers between patches and that the predator disperses between the patches with no barrier. Conditions are derived for the global asymptotic stability of a positive equilibrium.     

Periodic Solution and Stationary Distribution of Stochastic Predator–Prey Models with Higher-Order Perturbation

In this paper, two stochastic predator–prey models with general functional response and higher-order perturbation are proposed and investigated. For the nonautonomous periodic case of the system, by using Khasminskii’s theory of periodic solution, we show that the system admits a nontrivial positive T-periodic solution. For the system disturbed by both white and telegraph noises, sufficient conditions for positive recurrence and the existence of an ergodic stationary distribution to the solutions are established. The existence of stationary distribution implies stochastic weak stability to some extent.     

Predator–Prey model with Holling response function of type II and SIS infectious disease

We analyze the influence of a SIS infectious disease affecting Preys or both Predators and Preys in a Predator–Prey model. The response function used here is Holling function type II. Many thresholds are computed and used to investigate the global stability results. The disease can disappear from the community, persist in one or two populations of the community. At least one population can disappear from the community because of disease. In some cases, the model exhibits periodic solutions with persistence of the disease or without disease. Numerical simulations are used with nonstandard numerical schemes to illustrate our results.     

Periodic Solutions of a Delayed Predator-Prey Model with Stage Structure for Prey

A periodic predator-prey model with stage structure for prey and time delays due to negative feed-back and gestation of predator is proposed.By using Gaines and Mawhin's continuation theorem of coincidencedegree theory,sufficient conditions are derived for the existence of positive periodic solutions to the proposedmodel.Numerical simulations are presented to illustrate the feasibility of our main result.     

Predator–Prey Dynamics on Infinite Trees: A Branching Random Walk Approach

We are interested in predator–prey dynamics on infinite trees, which can informally be seen as particular two-type branching processes where individuals may die (or be infected) only after their parent dies (or is infected). We study two types of such dynamics: the chase–escape process, introduced by Kordzakhia with a variant by Bordenave who sees it as a rumor propagation model, and the birth-and-assassination process, introduced by Aldous and Krebs. We exhibit a coupling between these processes and branching random walks killed at the origin. This sheds new light on the chase–escape and birth-and-assassination processes, which allows us to recover by probabilistic means previously known results and also to obtain new results. For instance, we find the asymptotic behavior of the tail of the number of infected individuals in both the subcritical and critical regimes for the chase–escape process and show that the birth-and-assassination process ends almost surely at criticality.     

A Predator�CPrey Model with a Holling Type I Functional Response Including a Predator Mutual Interference

The most widely used functional response in describing predator–prey relationships is the Holling type II functional response, where per capita predation is a smooth, increasing, and saturating function of prey density. Beddington and DeAngelis modified the Holling type II response to include interference of predators that increases with predator density. Here we introduce a predator-interference term into a Holling type I functional response. We explain the ecological rationale for the response and note that the phase plane configuration of the predator and prey isoclines differs greatly from that of the Beddington–DeAngelis response; for example, in having three possible interior equilibria rather than one. In fact, this new functional response seems to be quite unique. We used analytical and numerical methods to show that the resulting system shows a much richer dynamical behavior than the Beddington–DeAngelis response, or other typically used functional responses. For example, cyclic-fold, saddle-fold, homoclinic saddle connection, and multiple crossing bifurcations can all occur. We then use a smooth approximation to the Holling type I functional response with predator mutual interference to show that these dynamical properties do not result from the lack of smoothness, but rather from subtle differences in the functional responses.     

Qualitative Analysis of a Belousov–Zhabotinskii Reaction Model

This paper deals with one kind of Belousov–Zhabotinskii reaction model. Linear stability is discussed for the spatially homogeneous problem firstly. Then we focus on the stationary problem with diffusion. Non-existence and existence of non-constant positive solutions are obtained by using implicit function theorem and Leray–Schauder degree theory, respectively.     

Homogenized Diffusion Limit of a Vlasov–Poisson–Fokker–Planck Model

The approximation by diffusion and homogenization of the initial-boundary value problem of the Vlasov–Poisson–Fokker–Planck model is studied for a given velocity field with spatial macroscopic and microscopic variations. The L¹-contraction property of the Fokker–Planck operator and a two-scale Hybrid-Hilbert expansion are used to prove the convergence towards a homogenized Drift–Diffusion equation and to exhibit a rate of convergence.     

On a Boolean-valued Model of the Strict Implication System(Continuous)

The reference [4] proved the consistency of S1 and S2 among Lewis' five strict implication systems in the modal logic by using the method of the Boolean-valued model. But, in this method, the consistency of S3, S4 and S5 in Lewis' five strict implication systems is not decided. This paper makes use of the properties: (1) the equivalence of the modal systems S3 and P3, S4 and P4; (2) the modal systems P3 and P4 all contained the modal axiom T(□p → p); (3) the modal axiom T is correspondence to the reflexive property in VB. Hence, the paper proves: (a) ‖As31‖ = 1; (b) ‖AS41‖ = 1; (c) ‖AS5l‖ = 1 in the model (where B is a complete Boolean algebra, R is reflexive property in VB). Therefore, the paper finally proves that the Boolean-valued model VB of the ZFC axiom system in set theory is also a Boolean-valued model of Lewis' the strict implication system S3, S4 and S5.     

Exact Controllability of a Faedo–Galërkin Scheme for the Dynamics of Polymer Fluids

Journal of Optimization Theory and Applications - We describe the dynamics of fluids with scattered polymer chains through a multi-field model accounting for weakly non-local inertia and...