• Bulletin of the Korean Mathematical Society
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• v.47 no.2
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• pp.251-261
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• 2010

This paper deals with a predator-prey model with Holling type III response function and cross-diffusion subject to the homogeneous Neumann boundary condition. We first give a priori estimates (positive upper and lower bounds) of positive steady states. Then the non-existence and existence results of non-constant positive steady states are given as the cross-diffusion coefficient is varied, which means that stationary patterns arise from cross-diffusion.

• Bulletin of the Korean Mathematical Society
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• v.50 no.6
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• pp.1827-1840
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• 2013

This paper is concerned with the positive steady states of a diffusive Holling type II predator-prey system, in which two predators and one prey are involved. Under homogeneous Neumann boundary conditions, the local and global asymptotic stability of the spatially homogeneous positive steady state are discussed. Moreover, the large diffusion of predator is considered by proving the nonexistence of non-constant positive steady states, which gives some descriptions of the effect of diffusion on the pattern formation.

• Journal of the Korean Society for Industrial and Applied Mathematics
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• v.14 no.4
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• pp.225-247
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• 2010

In this paper, we establish a two-competitive-prey and one-predator Holling type II system by introducing a proportional periodic impulsive harvesting for all species and a constant periodic releasing, or immigrating, for the predator at different fixed time. We show the boundedness of the system and find conditions for the local and global stabilities of two-prey-free periodic solutions by using Floquet theory for the impulsive differential equation, small amplitude perturbation skills and comparison techniques. Also, we prove that the system is permanent under some conditions and give sufficient conditions under which one of the two preys is extinct and the remaining two species are permanent. In addition, we take account of the system with seasonality as a periodic forcing term in the intrinsic growth rate of prey population and then find conditions for the stability of the two-prey-free periodic solutions and for the permanence of this system. We discuss the complex dynamical aspects of these systems via bifurcation diagrams.

• Journal of the Korean Mathematical Society
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• v.55 no.1
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• pp.43-58
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• 2018

In this paper, we study a delayed predator-prey system with Holling type IV functional response incorporating the effect of habitat complexity. The results show that there exist stability switches and Hopf bifurcation occurs while the delay crosses a set of critical values. The explicit formulas which determine the direction and stability of Hopf bifurcation are obtained by the normal form theory and the center manifold theorem.

• Journal of applied mathematics & informatics
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• v.29 no.3_4
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• pp.781-802
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• 2011

Of concern in the paper is a Holling-Tanner predator-prey model with modified version of the Leslie-Gower functional response. Dynamical behaviours such as stability, permanence and Hopf bifurcation have been carried out deterministically. Using the normal form theory and center manifold theorem, the explicit formulae determining the stability and direction of Hopf bifurcation have been derived. The deterministic model is extended to a stochastic one by perturbing the growth equation of prey and predator by white and colored noises and finally the mean square stability of the stochastic model systems is investigated analytically. An extensive quantitative analysis has been performed based on numerical computation so as to validate the applicability of the proposed mathematical model.

• Korean journal of applied entomology
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• v.35 no.2
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• pp.126-131
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• 1996

These experiments were conducted in the laboratory conditions to determine the prey consumption of a predaciousphytoseiid mite, Amblyseius womersleyi Schicha, and its ability to regulate the population of tea redspider mite, Tetranychus kanzawai Kishida. The functional response curve of the adult A. womersleyi to thedensity of eggs, larvae, and nymphs of T. kanzawai indicated Holling's Type 11: the consumption of prey bythe adult A. womersleyi increased with the prey density but the consumption rate decreased. The critical initialratio to suppress the prey population by the predator seemed to be 32:l @rey:predator) at 25"C, and 16:l at20$^{\circ}$C on kidney bean plant. The predator could not regulate any initial ratio of the prey population at 15$^{\circ}$C.^{\circ}$C.

• The Pure and Applied Mathematics
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• v.17 no.3
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• pp.211-229
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• 2010

Various types of predator-prey systems are studied in terms of the stabilities of their steady-states. Necessary conditions for the existences of non-negative constant steady-states for those systems are obtained. The linearized stabilities of the non-negative constant steady-states for the predator-prey system with monotone response functions are analyzed. The predator-prey system with non-monotone response functions are also investigated for the linearized stabilities of the positive constant steady-states.

• Journal of applied mathematics & informatics
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• v.5 no.3
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• pp.597-606
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• 1998

In the present study we consider a mathematical model of a non-interactive type autotroph-herbivore system in which the amount of autotroph biomass consumed by the herbivore is assumed to follow a Holling type II functional response. We have also incorpo-rated discrete time delays in the numerical response term to represent a delay due to gestation and in the recycling term which represent a delay due to gestation and in the recycling term which represents the time required for bacterial decomposition. We have derived con-dition for global asymptotic stability of the model in the absence of delays. Conditions for delay-induced asymptotic stability of the steady state are also derived. The length of the delay preserving stability has been estimated and interpreted ecologically.

• Communications of the Korean Mathematical Society
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• v.23 no.2
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• pp.211-227
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• 2008

As a mathematical model proposed to understand the behaviors of interacting species, cross-diffusion systems with functional responses of prey-predator type are considered. In order to obtain $W^{1_2}$-estimates of the solutions, we make use of several forms of calculus inequalities and embedding theorems. We consider the quasilinear parabolic systems with the cross-diffusion terms, and without the self-diffusion terms because of the simplicity of computations. As the main result we derive the uniform $W^{1_2}$-bound of the solutions and obtain the global existence in time.

• 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.