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.     

A simple Gause‐type predator–prey model considering social predation

The consumer–resource relationships are among the most fundamental of all ecological relationships and have been the focus of ecology since its beginnings. Usually are described by nonlinear differential equation systems, putting the emphasis in the effect of antipredator behavior (APB) by the prey; nevertheless, a minor quantity of articles has considered the social behavior of predators. In this work, two predator–prey models derived from the Volterra model are analyzed, in which the equation of predators is modified considering cooperation or collaboration among predators. It is well known that competition among predators produces a stabilizing effect on system describing the model, since there exists a wide set in the parameter space where the system has a unique equilibrium point in the phase plane, which is globally asymptotically stable. Meanwhile, the cooperation can originate more complex and unusual dynamics. As we will show, it is possible to prove that for certain subset of parameter values the predator population sizes tend to infinite when the prey population goes to extinct. This apparently contradicts the idea of a realistic model, when it is implicitly assumed that the predators are specialist, ie, the prey is its unique source of food. However, this could be a desirable effect when the prey constitutes a plague. To reinforce the analytical result, numerical simulations are presented.     

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.     

Asymptotic dynamics of a deterministic and stochastic predator–prey model with disease in the prey species

In this paper, we discuss a predator–prey model with the Beddington–DeAngelis functional response of predators and a disease in the prey species. At first we study permanence and global stability of a positive equilibrium for the deterministic version of the model. Then we include a stochastic perturbation of the white noise type. We analyse the influence of this stochastic perturbation on the systems and prove that the positive equilibrium is also globally asymptotically stable in this case. The key point of our analysis is to choose appropriate Lyapunov functionals. We point out the differences between the deterministic and stochastic versions of the model. Copyright © 2013 John Wiley & Sons, Ltd.     

Limit cycles in a generalized Gause-type predator–prey model

We study the problem of the existence of limit cycles for a generalized Gause-type predator–prey model with functional and numerical responses that satisfy some general assumptions. These assumptions describe the effect of prey density on the consumption and reproduction rates of predator. The model is analyzed for the situation in which the conversion efficiency of prey into new predators increases as prey abundance increases. A necessary and sufficient condition for the existence of limit cycles is given. It is shown that the existence of a limit cycle is equivalent to the instability of the unique positive critical point of the model. The results can be applied to the analysis of many models appearing in the ecological literature for predator–prey systems. Some ecological models are given to illustrate the 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.     

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.     

Dynamics and pattern formations in diffusive predator‐prey models with two prey‐taxis

A reaction‐diffusion two‐predator‐one‐prey system with prey‐taxis describes the spatial interaction and random movement of predator and prey species, as well as the spatial movement of predators pursuing preys. The global existence and boundedness of solutions of the system in bounded domains of arbitrary spatial dimension and any small prey‐taxis sensitivity coefficient are investigated by the semigroup theory. The spatial pattern formation induced by the prey‐taxis is characterized by the Turing type linear instability of homogeneous state; it is shown that prey‐taxis can both compress and prompt the spatial patterns produced through diffusion‐induced instability in two‐predator‐one‐prey systems.     

Predator–prey harvesting model with fatal disease in prey

A theoretical eco‐epidemiological model of a prey–predator interaction system with disease in prey species is studied. Predator consumes both susceptible and infected prey population, but predator also feeds preferentially on many numerous species, which are over represented in the predator's diet. Equilibrium points of the system are determined, and the dynamic behaviour of the system is investigated around equilibrium points. Death rate of predator species is considered as a bifurcation parameter to examine the occurrence of Hopf bifurcation in the neighbourhood of the coexisting equilibria. Numerical simulations are carried out to support the analytical results. Copyright © 2015 John Wiley & Sons, Ltd.     

On a stoichiometric two predators on one prey discrete model

In this letter, we first propose a discrete analogue of a continuous time predator–prey system, which models the dynamics of two predators on one prey [I. Loladze, Y. Kuang, J. Elser, W.F. Fagan, Competition and stoichiometry: Coexistence of two predators on one prey, Theor. Popul. Biol. 65 (2004) 1–15]. Then, we study the dynamics of this discrete model. We establish results on boundedness and global attractivity. Finally, several numerical simulations are given to support the theoretical results.     

Existence of global solutions for a three‐species predator‐prey model with cross‐diffusion

In this short note, we study a strongly coupled system of partial differential equations which models the dynamics of a two‐predator‐one‐prey ecosystem in which the prey exercises defense switching and the predators collaboratively take advantage of the prey's strategy. We prove the existence of global strong solutions. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Disease‐selective predation may lead to prey extinction

In real world bio‐communities, predational choice plays a key role to the persistence of the prey population. Predator's ‘sense’ of choice for predation towards the infected and noninfected prey is an important factor for those bio‐communities. There are examples where the predator can distinguish the infected prey and avoids those at the time of predation. Based on the examples, we propose two mathematical models and observe the dynamics of the systems around biologically feasible equilibria. For disease‐selective predation model there is a high risk of prey extinction. On the other hand, for non‐disease selective predation both populations co‐exist. Local stability analysis and global stability analysis of the positive interior equilibrium are performed. Moreover, conditions for the permanence of the system are obtained. Finally, we conclude that strictly disease‐selective predation may not be acceptable for the persistence of the prey population. Copyright © 2005 John Wiley & Sons, Ltd.     

General functional response and recruitment in a predator–prey system with capture on both species

This work provides a mathematical model for a predator‐prey system with general functional response and recruitment, which also includes capture on both species, and analyzes its qualitative dynamics. The model is formulated considering a population growth based on a general form of recruitment and predator functional response, as well as the capture on both prey and predators at a rate proportional to their populations. In this sense, it is proved that the dynamics and bifurcations are determined by a two‐dimensional threshold parameter. Finally, numerical simulations are performed using some ecological observations on two real species, which validate the theoretical results obtained. Copyright © 2014 John Wiley & Sons, Ltd.     

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.     

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 $R_0<1$.     

Interactive effects of prey refuge and additional food for predator in a diffusive predator-prey system

Additional food for predators has been considered as one of the best established techniques in integrated pest management and biological conservation programs. In natural systems, there are several other factors, e.g., prey refuge, affect the success of pest control. In this paper, we analyze a predator-prey system with prey refuge and additional food for predator apart from the focal prey in the presence of diffusion. Our main aim is to study the interactive effects of prey refuge and additional food on the system dynamics and especially on the controllability of prey (pest). Different types of Turing patterns such as stripes, spots, holes, and mixtures of them are obtained. It is found that the supply of additional food to the predator is unable to control the prey (pest) population when prey refuge is high. Moreover, when both prey refuge and additional food are low, spatial distribution of prey becomes complex and once again prey control becomes difficult. However, the joint effect of reduction in prey refuge and the presence of appropriate amount of additional food can control prey (pest) population from the system.     

Traveling wave solutions of Lotka–Volterra type two predators‐one prey model

In this work, we consider a model with one basal resource and two species of predators feeding by the same resource. There are three non‐trivial boundary equilibria. One is the saturated state E_K of the prey without any predator. Other two equilibria, E₁ and E₂, are the coexistence states of the prey with only one species of predators. Using a high‐dimensional shooting method, the Wazewski' principle, we establish the conditions for the existence of traveling wave solutions from E_K to E₂ and from E₁ to E₂. These results show that the advantageous species v₂ always win in the competition and exclude species v₁ eventually. Finally, some numerical simulations are presented, and biological interpretations are given. Copyright © 2016 John Wiley & Sons, Ltd.     

Periodic solutions in non autonomous predator prey system with delays

In this paper, we consider a biological model for two predators and one prey with periodic delays. By assuming that one predator consumes prey according to Holling II functional response while the other predator consumes prey according to the Beddington–DeAngelis functional response, based on the coincidence degree theory, the existence of positive periodic solutions for this model is obtained under suitable conditions.     

Multiple periodic solutions of a delayed stage-structured predator–prey model with non-monotone functional responses

A delayed stage-structured predator–prey model with non-monotone functional responses is proposed. It is assumed that immature individuals and mature individuals of the predator are divided by a fixed age, and that immature predators do not have the ability to attack prey. Some new and interesting sufficient conditions are obtained for the global existence of multiple positive periodic solutions of the stage-structured predator–prey model. Our method is based on Mawhin’s coincidence degree and novel estimation techniques for the a priori bounds of unknown solutions to Lx = λNx. An example is given to illustrate the feasibility of our main result.     

An impulsive predator–prey model with disease in the prey for integrated pest management

In this paper, an impulsive predator–prey model with disease in the prey is investigated for the purpose of integrated pest management. In the first part of the main results, we get the sufficient condition for the global stability of the susceptible pest-eradication periodic solution. This means if the release amount of infective prey and predator satisfy the condition, then the pest will be doomed. In the second part of the main results, we also get the sufficient condition for the permanence of the system. This means if the release amount of infective prey and predator satisfy the condition, then the prey and the predator will coexist. In the last section, we interpret our mathematical results. We also point out some possible future work.