Chaos in delay-induced Leslie–Gower prey–predator–parasite model and its control through prey harvesting

In this paper we analyze a delay-induced predator–prey–parasite model with prey harvesting, where the predator–prey interaction is represented by Leslie–Gower type model with type II functional response. Infection is assumed to spread horizontally from one infected prey to another susceptible prey following mass action law. Spreading of disease is not instantaneous but mediated by a time lag to take into account the time required for incubation process. Both the susceptible and infected preys are subjected to linear harvesting. The analysis is accomplished in two phases. First we analyze the delay-induced predator–prey–parasite system in absence of harvesting and proved the local & global dynamics of different (six) equilibrium points. It is proved that the delay has no influence on the stability of different equilibrium points except the interior one. Delay may cause instability in an otherwise stable interior equilibrium point of the system and larger delay may even produce chaos if the infection rate is also high. In the second phase, we explored the dynamics of the delay-induced harvested system. It is shown that harvesting of prey population can suppress the abrupt fluctuations in the population densities and can stabilize the system when it exceeds some threshold value.     

A study of harvesting in a predator–prey model with disease in both populations

Disease control by managers is a crucial response to emerging epidemics, and in the context of global change, emerging risks associated with parasites, invasive species, and infectious diseases are an important issue especially for developing countries. Our objective is to provide a mathematical framework to study the response of a predator–prey model to a disease in both populations and harvesting of prey species. We have worked out the conditions for local stability of the equilibrium points as well as persistence of the system. We have derived the ecological and disease basic reproduction numbers. These enable us to determine the community structure of the system. Harvesting may play a crucial role in a host–parasite system, and reasonable harvesting can remove parasite burden from the host. Our numerical results reveal that the reasonable harvesting prevents the oscillations of the species. We conclude that harvesting can be an effective strategy for controlling the spread of disease. Copyright © 2016 John Wiley & Sons, Ltd.     

Nonselective harvesting of a prey-predator community with infected prey

The present paper deals with the problem of nonselective harvesting in a partly infected prey and predator system in which both the susceptible prey and the predator follow the law of logistic growth and some preys avoid predation by hiding. The dynamical behaviour of the system has been studied in both the local and global sense. The optimal policy of exploitation has been derived by using Pontraygin’s maximal principle. Numerical analysis and computer simulation of the results have been performed to investigate the global properties of the system.     

Novel dynamics of a predator–prey system with harvesting of the predator guided by its population

A predator–prey model was extended to include nonlinear harvesting of the predator guided by its population, such that harvesting is only implemented if the predator population exceeds an economic threshold. The proposed model is a nonsmooth dynamic system with switches between the original predator-prey model (free subsystem) and a model with nonlinear harvesting (harvesting subsystem). We initially examine the dynamics of both the free and the harvesting subsystems, and then we investigate the dynamics of the switching system using theories of nonsmooth systems. Theoretical results showed that the harvesting subsystem undergoes multiple bifurcations, including saddle-node, supercritical Hopf, Bogdanov–Takens and homoclinic bifurcations. The switching system not only retains all of the complex dynamics of the harvesting system but also exhibits much richer dynamics such as a sliding equilibrium, sliding cycle, boundary node (saddle point) bifurcation, boundary saddle-node bifurcation and buckling bifurcation. Both theoretical and numerical results showed that, by implementing predator population guided harvesting, the predator and prey population could coexist in more scenarios than those in which the predator may go extinct for the continuous harvesting regime. They could either stabilize at an equilibrium or oscillate periodically depending on the value of the economic threshold and the initial value of the system.     

A cannibalistic eco-epidemiological model with disease in predator population

In this present article, we propose and analyze a cannibalistic predator–prey model with disease in the predator population. We consider two important factors for the dynamics of predator population. The first one is governed through cannibalistic interaction, and the second one is governed through the disease in the predator population via cannibalism. The local stability analysis of the model system around the biologically feasible equilibria are investigated. We perform global dynamics of the model using Lyapunov functions. We analyze and compare the community structure of the system in terms of ecological and disease basic reproduction numbers. The existence of Hopf bifurcation around the interior steady state is investigated. We also derive the sufficient conditions for the permanence and impermanence of the system. The study reveals that the cannibalism acts as a self-regulatory mechanism and controls the disease transmission among the predators by stabilizing the predator–prey oscillations.     

An ecoepidemiological predator‐prey model with standard disease incidence

This investigation accounts for epidemics spreading among interacting populations. The infective disease spreads among the prey, of which only susceptibles reproduce, while infected prey do not grow, recover, reproduce nor compete for resources. The model is general enough to describe a large number of ecosystems, on land, in the air or in the water. The main results concern the boundedness of the trajectories, the analysis of local and global stability, system's persistency and a threshold property below which the infection disappears. A sufficiently strong disease in the prey may avoid predators extinction and its presence can destabilize an otherwise stable predator‐prey configuration. The occurrence of transcritical, saddle‐node and Hopf‐bifurcations is also shown. Copyright © 2008 John Wiley & Sons, Ltd.     

Effect of diffusion on a two-species eco-epidemiological model

This paper deals with the stabilizing effect of diffusion on a prey?–?predator system where the prey population is infected by a microparasite. The predator functional response is a concave-type function. Conditions for the local as well as global stability of the model without diffusion are derived in terms of system parameters. It is also shown that an unstable equilibrium of the model without diffusion can be made stable by increasing the diffusion coefficients appropriately.     

Modeling and analysis of a modified Leslie–Gower type three species food chain model with an impulsive control strategy

This paper describes a modified Leslie–Gower type three species food chain model with harvesting. We have incorporated impulsive control strategy to the system. Theories of impulsive differential equations, small amplitude perturbation skills and comparison technique are used to study dynamical behavior of the system. Sufficient conditions are derived to ensure global stability of the lowest-level prey and mid-level predator eradication periodic solution. Sufficient conditions are also derived to examine the permanence of the system. Numerical simulations are carried out to verify the analytical results, and the system is analyzed through graphical illustrations. It is observed that the stability of the system exhibits several states, ranging from stable situation to cyclic oscillatory behavior, under different favorable conditions. These results are useful to study the dynamic complexity of ecological systems. The computation of the largest Lyapunov exponent demonstrates the chaotic dynamic nature of the system. The qualitative nature of strange attractor is examined. It is to be noted that the harvesting effort can cause a stable equilibrium to become unstable and even a switching of stabilities.     

Modeling and analysis of a prey–predator system with disease in the prey

A three dimensional ecoepidemiological model consisting of susceptible prey, infected prey and predator is proposed and analysed in the present work. The parameter delay is introduced in the model system for considering the time taken by a susceptible prey to become infected. Mathematically we analyze the dynamics of the system such as, boundedness of the solutions, existence of non-negative equilibria, local and global stability of interior equilibrium point. Next we choose delay as a bifurcation parameter to examine the existence of the Hopf bifurcation of the system around its interior equilibrium. Moreover we use the normal form method and center manifold theorem to investigate the direction of the Hopf bifurcation and stability of the bifurcating limit cycle. Some numerical simulations are carried out to support the analytical results.     

Influence of prey reserve in a prey–predator fishery

The excessive and unsustainable exploitation of marine resources has to led to the promotion of marine reserve as a fisheries management tool. In this paper we study a prey–predator system in a two-patch environment: one accessible to both prey and predators (patch 1) and the other one being a refuge for the prey (patch 2). The prey refuge (patch 2) constitutes a reserve zone of prey and fishing is not permitted, while the unreserved zone area is an open-access fishery zone. The existence of possible steady states, along with their local and global stability, is discussed. We then examine the possibilities of the existence of bionomic equilibrium. An optimal harvesting policy is given using Pontryagin’s maximum principle.     

Modelling and analysis of a harvested prey–predator system incorporating a prey refuge

The present paper deals with a prey–predator model incorporating a prey-refuge and independent harvesting in either species. Our study shows that, using the harvesting efforts as controls, it is possible to break the cyclic behaviour of the system and drive it to a required state. The possibility of existence of bionomic equilibria has been considered. The problem of optimal harvest policy is then solved by using Pontryagin's maximal principle.     

基于食饵保护的食饵-捕食捕鱼模型分析(英文)

In this paper,we consider a prey-predator fishery model with prey dispersal in a two-patch environment,one is assumed to be a free fishing zone and the other is a reserved zone where fishing and other extractive activities are prohibited.The existence of possible steady states of the system is discussed.The local and global stability analysis has been carried out.An optimal harvesting policy is given using Pontryagin s maximum principle.     

A prey-predator model with harvesting for fishery resource with reserve area

Considering that over exploitation would result in the extinction of the population, we propose and investigate a Holling II functional response prey-predator model with harvesting for fishery resource in a two-patch environment: a free fishing zone (patch 1) and a reserve zone (patch 2) where fishing is strictly prohibited. First, the presence of harvesting can impact the existence of equilibria. Further, stability criteria of the model is analyzed both from local and global point of view. Our results indicate that so long as the prey population in the reserved zone does not extinct, the both prey always exist, that is marine reserves should ensure the sustainability of system. Thus, marine reserves not only protect species inside the reserve area but they can also increase fish abundance in adjacent areas. Next, the existence of bionomic equilibrium and the optimal harvesting policy are discussed. The present value of revenues is maximized by using Pontryagin’s maximum principle. It is established that an infinite discount rate leads to complete dissipation of economic rent. Finally, some numerical simulations are given to illustrate our results.     

Effect of emergent carrying capacity in an eco‐epidemiological system

The paper explores an eco‐epidemiological model of a predator–prey type, where the prey population is subject to infection. The model is basically a combination of S‐I type model and a Rosenzweig–MacArthur predator–prey model. The novelty of this contribution is to consider different competition coefficients within the prey population, which leads to the emergent carrying capacity. We explicitly separate the competition between non‐infected and infected individuals. This emergent carrying capacity is markedly different to the explicit carrying capacities that have been considered in many eco‐epidemiological models. We observed that different intra‐class and inter‐class competition can facilitate the coexistence of susceptible prey‐infected prey–predator, which is impossible for the case of the explicit carrying capacity model. We also show that these findings are closely associated with bi‐stability. The present system undergoes bi‐stability in two different scenarios: (a) bi‐stability between the planner equilibria where susceptible prey co‐exists with predator or infected prey and (b) bi‐stability between co‐existence equilibrium and the planner equilibrium where susceptible prey coexists with infected prey; have been discussed. The conditions for which the system is to be permanent and the global stability of the system around disease‐free equilibrium are worked out. Copyright © 2015 John Wiley & Sons, Ltd.     

Eco-epidemiological model with fatal disease in the prey

We investigate a model consisting of a predator population and both susceptible and infected prey populations. The predator can feed on either prey species but instead of choosing individuals at random the predator feeds preferentially on the most abundant prey species. More specifically we assume that the likelihood of a predator catching a susceptible prey or an infected prey is proportional to the numbers of these two different types of prey species. This phenomenon, involving changing preference from susceptible to infected prey, is called switching. Mukhopadhyay studied a switching model and proposed that the interaction of predators with infected prey is beneficial for the growth of the predator. In this model, we assume that the predator will eventually die as a result of eating infected prey. We find a threshold parameter $R_0$ and showed that the disease will be eradicated from the system if $R_0<1$.     

Homoclinic bifurcation for a general state-dependent Kolmogorov type predator–prey model with harvesting

In this paper, a general Kolmogorov type predator–prey model is considered. Together with a constant-yield predator harvesting, the state dependent feedback control strategies which take into account the impulsive harvesting on predators as well as the impulsive stocking on the prey are incorporated in the process of population interactions. We firstly study the existence of an order-1 homoclinic cycle for the system. It is shown that an order-1 positive periodic solution bifurcates from the order-1 homoclinic cycle through a homoclinic bifurcation as the impulsive predator harvesting rate crosses some critical value. The uniqueness and stability of the order-1 positive periodic solution are derived by applying the geometry theory of differential equations and the method of successor function. Finally, some numerical examples are provided to illustrate the main results. These results indicate that careful management of resources and harvesting policies is required in the applied conservation and renewable resource contexts.     

Pest control may make the pest population explode

We present an example of a predator-prey-like system with a prey-only state as a global attractor, and with the additional property that an attempt to control the prey by harvesting or poisoning both species produces solutions in which both populations blow up in finite time.     

Pest control may make the pest population explode

We present an example of a predator-prey-like system with a prey-only state as a global attractor, and with the additional property that an attempt to control the prey by harvesting or poisoning both species produces solutions in which both populations blow up in finite time.     

Predator–prey interaction with harvesting: mathematical study with biological ramifications

In this article, we study a simple predator–prey interaction where predator population is subjected to harvesting. Our qualitative analysis shows different outcomes including switching of stability, oscillations and deterministic extinction. Theoretically observed results have been tested with the parameter values of Paramecium aurelia and its predator Didinium nasutum. Study reveals that harvesting effort and predator’s attack rate may be used as control parameters for the system. Simulation results also indicate that the system may exhibit bistability for some parametric region. Our study also gives the possible answer to the question – why do we frequently observe coexisting predator–prey system in natural system? The study may be helpful to design control strategy for harvested predator–prey system.     

Dynamics analysis of a reaction–diffusion system with Beddington–DeAngelis functional response and strong Allee effect

In this paper, the dynamics of a diffusive predator–prey model with modified Leslie–Gower term and strong Allee effect on prey under homogeneous Neumann boundary condition is considered. Firstly, we obtain the qualitative properties of the system including the existence of the global positive solution and the local and global asymptotical stability of the constant equilibria. In addition, we investigate a priori estimate and the nonexistence of nonconstant positive steady state solutions. Finally, we establish the existence and local structure of steady state patterns and time-periodic patterns for the system.