• Kyungpook Mathematical Journal
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• v.56 no.1
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• pp.47-55
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• 2016

In this paper, we consider a discrete predator-prey system obtained from a continuous Beddington-DeAngelis type predator-prey system by using the method in [9]. In order to investigate dynamical behaviors of this discrete system, we find out all equilibrium points of the system and study their stability by using eigenvalues of a Jacobian matrix for each equilibrium points. In addition, we illustrate some numerical examples in order to substantiate theoretical results.

• Journal of applied mathematics & informatics
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• v.40 no.3_4
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• pp.393-407
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• 2022

In this paper, a diffusive predator-prey system with Beddington DeAngelis functional response and the modified Leslie-Gower type predator dynamics when a prey population is infected is considered. The predator is assumed to predate both the susceptible prey and infected prey following the Beddington-DeAngelis functional response and Holling type II functional response, respectively. The predator follows the modified Leslie-Gower predator dynamics. Both the prey, susceptible and infected, and predator are assumed to be distributed in-homogeneous in space. A reaction-diffusion equation with Neumann boundary conditions is considered to capture the dynamics of the prey and predator population. The global attractor and persistence properties of the system are studied. The priori estimates of the non-constant positive steady state of the system are obtained. The existence of non-constant positive steady state of the system is investigated by the use of Leray-Schauder Theorem. The existence of non-constant positive steady state of the system, with large diffusivity, guarantees for the occurrence of interesting Turing patterns.

• Journal of applied mathematics & informatics
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• v.24 no.1_2
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• pp.127-139
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• 2007

In this paper, we investigate a discrete-time non-autonomous predator-prey system with the Beddington-DeAngelis functional response. By using the coincidence degree and the related continuation theorem as well as some priori estimates, easily verifiable sufficient criteria are established for the existence of positive periodic solutions.

• Kyungpook Mathematical Journal
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• v.49 no.4
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• pp.605-618
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• 2009

A stage-structured predator-prey system with time delay and Beddington-DeAngelis functional response is considered. By analyzing the corresponding characteristic equation, the local stability of a positive equilibrium is investigated. The existence of Hopf bifurcations is established. Formulae are derived to determine the direction of bifurcations and the stability of bifurcating periodic solutions by using the normal form theory and center manifold theorem. Numerical simulations are carried out to illustrate the theoretical results.

• Journal of the Chungcheong Mathematical Society
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• v.26 no.4
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• pp.749-756
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• 2013

In this paper, we consider a diffusive delayed predator-prey model with Beddington-DeAngelis type functional response under homogeneous Neumann boundary conditions, where the discrete time delay covers the period from the birth of immature preys to their maturity. We investigate the global existence of nonnegative solutions and the long-term behavior of the time-dependent solution of the model.

• Journal of the Korean Mathematical Society
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• v.49 no.4
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• pp.779-794
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• 2012

In this paper, we study the global stability of two mathematical models for human immunodeficiency virus (HIV) infection with intra-cellular delays. The first model is a 5-dimensional nonlinear delay ODEs that describes the interaction of the HIV with two classes of target cells, $CD4^+$ T cells and macrophages taking into account the saturation infection rate. The second model generalizes the first one by assuming that the infection rate is given by Beddington-DeAngelis functional response. Two time delays are used to describe the time periods between viral entry the two classes of target cells and the production of new virus particles. Lyapunov functionals are constructed and LaSalle-type theorem for delay differential equation is used to establish the global asymptotic stability of the uninfected and infected steady states of the HIV infection models. We have proven that if the basic reproduction number $R_0$ is less than unity, then the uninfected steady state is globally asymptotically stable, and if the infected steady state exists, then it is globally asymptotically stable for all time delays.