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1.
We investigate the qualitative behavior of a host‐parasitoid model with a strong Allee effect on the host. More precisely, we discuss the boundedness, existence and uniqueness of positive equilibrium, local asymptotic stability of positive equilibrium and existence of Neimark–Sacker bifurcation for the given system by using bifurcation theory. In order to control Neimark–Sacker bifurcation, we apply pole‐placement technique that is a modification of OGY method. Moreover, the hybrid control methodology is implemented in order to control Neimark–Sacker bifurcation. Numerical simulations are provided to illustrate theoretical discussion. Copyright © 2017 John Wiley & Sons, Ltd.  相似文献   

2.
赵延忠 《大学数学》2011,27(5):21-26
讨论一类具有Allee影响的捕食者-食饵扩散模型解的整体性态.通过线性化方法和Lyapunov泛函方法分别证明了该模型正平衡点的局部渐近稳定性和全局渐近稳定性.  相似文献   

3.
We study a discrete host–parasitoid system where the host population follows the classical Ricker functional form and is also subject to Allee effects. We determine basins of attraction of the local attractors of the single population model when the host intrinsic growth rate is not large. In this situation, existence and local stability of the interior steady states for the host–parasitoid interaction are completely analysed. If the host's intrinsic growth rate is large, then the interaction may support multiple interior steady states. Linear stability of these steady states is provided.  相似文献   

4.
The goal of this work is to examine the global behavior of a Gause‐type predator–prey model in which two aspects have been taken into account: (i) the functional response is Holling type III; and (ii) the prey growth is affected by a weak Allee effect. Here, it is proved that the origin of the system is a saddle point and the existence of two limit cycles surround a stable positive equilibrium point: the innermost unstable and the outermost stable, just like with the strong Allee effect. Then, for determined parameter constraints, the trajectories can have different ω ? limit sets. The coexistence of a stable limit cycle and a stable positive equilibrium point is an important fact for ecologists to be aware of the kind of bistability shown here. So, these models are undoubtedly rather sensitive to disturbances and require careful management in applied contexts of conservation and fisheries. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

5.
We present two general discrete-time host–parasitoid models with Allee effects on the host. In the first model, it is assumed that parasitism occurs prior to density dependence, while in the second model we assume that density dependence operates first followed by parasitism. It is shown that both models have similar asymptotic behaviour. The parasitoid population will definitely go extinct if the maximal growth rate of the host population is less than or equal to one, independent of whether density dependence or parasitism occurs first. The fate of the population is initial condition dependent if this maximal growth rate exceeds one. In particular, there exists a host population threshold, the Allee threshold, below which the host population goes extinct and so does the parasitoid. This threshold is the same for both models. Numerical examples with different functions are simulated to illustrate our analytical results.  相似文献   

6.
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.  相似文献   

7.
In this paper, we present a two species amensalism model with non-monotonic functional response and Allee effect on second species. Local and global stability of the boundary and interior equilibrium are investigated. By introducing the Allee effect, we show that the boundary equilibrium have changed from unstable node and saddle into saddle-node. Also, the system subject to an Allee effect has increased the time of reach to its stable steady-state solution, but has no influence on the final density of the two species. Our results are supported by numeric simulations.  相似文献   

8.
In this article, we propose and study a generalized Ricker–Beverton–Holt competition model subject to Allee effects to obtain insights on how the interplay of Allee effects and contest competition affects the persistence and the extinction of two competing species. By using the theory of monotone dynamics and the properties of critical curves for non-invertible maps, our analysis show that our model has relatively simple dynamics, i.e. almost every trajectory converges to a locally asymptotically stable equilibrium if the intensity of intra-specific competition intensity exceeds that of inter-specific competition. This equilibrium dynamics is also possible when the intensity of intra-specific competition intensity is less than that of inter-specific competition but under conditions that the maximum intrinsic growth rate of one species is not too large. The coexistence of two competing species occurs only if the system has four interior equilibria. We provide an approximation to the basins of the boundary attractors (i.e. the extinction of one or both species) where our results suggests that contest species are more prone to extinction than scramble ones are at low densities. In addition, in comparison to the dynamics of two species scramble competition models subject to Allee effects, our study suggests that (i) Both contest and scramble competition models can have only three boundary attractors without the coexistence equilibria, or four attractors among which only one is the persistent attractor, whereas scramble competition models may have the extinction of both species as its only attractor under certain conditions, i.e. the essential extinction of two species due to strong Allee effects; (ii) Scramble competition models like Ricker type models can have much more complicated dynamical structure of interior attractors than contest ones like Beverton–Holt type models have; and (iii) Scramble competition models like Ricker type competition models may be more likely to promote the coexistence of two species at low and high densities under certain conditions: At low densities, weak Allee effects decrease the fitness of resident species so that the other species is able to invade at its low densities; While at high densities, scramble competition can bring the current high population density to a lower population density but is above the Allee threshold in the next season, which may rescue a species that has essential extinction caused by strong Allee effects. Our results may have potential to be useful for conservation biology: For example, if one endangered species is facing essential extinction due to strong Allee effects, then we may rescue this species by bringing another competing species subject to scramble competition and Allee effects under certain conditions.  相似文献   

9.
We investigate the evolutionary outcomes of a single species population subject to Allee effects within the framework of a continuous strategy evolutionary game theory (EGT) model. Our model assumes a single trait creates a phenotypic trade-off between carrying capacity (i.e., competition) and predator evasion ability following a Gaussian distribution. This assumption contributes to one of our interesting findings that evolution prevents extinction even when population exhibits strong Allee effects. However, the extinction equilibrium can be an ESS under some special distributions of anti-predation phenotypes. The ratio of variation in competition and anti-predation phenotypes plays an important role in determining global dynamics of our EGT model: (a) evolution may suppress strong Allee effects for large values of this ratio; (b) evolution may preserve strong Allee effects for small values of this ratio by generating a low density evolutionary stable strategy (ESS) equilibrium which can serve as a potential Allee threshold; and (c) intermediate values of this ratio can result in multiple ESS equilibria.  相似文献   

10.
A model of host–parasitoid–hyperparasitoid is considered with ratio dependence between parasitoid and hyperparasitoid. First, the conditions for local stability and increasing host fitness due to the effect of hyperparasitism are deduced. Next, we study the effects of stochastic environmental fluctuations and discrete time delay on the system behavior and calculate the corresponding populations variances. Numerical simulations illustrate that populations densities oscillate randomly around equilibrium points. Also, in contrast to previous literature, the simulations carried out here indicate that populations variances oscillate with the increase of time delay.  相似文献   

11.
A model of three interacting populations where two populations engage in competition and two populations are in predator–prey type interaction is proposed and analysed. One of the two competing populations is subject to Allee effects and is also a pest population. The other competing population is regarded as a control agent and is the host for the predator population. There is a constant level of the external control agents released into the interaction at each generation after parasitism. We provide asymptotic dynamics of the competition subsystem and prove that a Neimark–Sacker bifurcation occurs for the host–parasitoid subsystem when the unique interior steady state loses its stability. The three interacting populations are impossible to persist for all positive initial conditions. Sufficient conditions based on the initial population size of the population with Allee effects are derived for persistence of the three populations.  相似文献   

12.
Since intraguild predation (IGP) is a ubiquitous and important community module in nature and Allee effect has strong impact on population dynamics, in this paper we propose a three-species IGP food web model consisted of the IG predator, IG prey and basal prey, in which the basal prey follows a logistic growth with strong Allee effect. We investigate the local and global dynamics of the model with emphasis on the impact of strong Allee effect. First, positivity and boundedness of solutions are studied. Then existence and stability of the boundary and interior equilibria are presented and the Hopf bifurcation curve at an interior equilibrium is given. The existence of a Hopf bifurcation curve indicates that if competition between the IG prey and IG predator for the basal resource lies below the curve then the interior equilibrium remains stable, while if it lies above the curve then the interior equilibrium loses its stability. In order to explore the impact of Allee effect, the parameter space is classified into sixteen different regions and, in each region, the number of interior equilibria is determined and the corresponding bifurcation diagrams on the Allee threshold are given. The extinction parameter regions of at least one species and the necessary coexistence parameter regions of all three species are provided. In addition, we explore possible dynamical patterns, i.e., the existence of multiple attractors. By theoretical analysis and numerical simulations, we show that the model can have one (i.e. extinction of all species), two (i.e. bi-stability) or three (i.e. tri-stability) attractors. It is also found by simulations that when there exists a unique stable interior equilibrium, the model may generate multiple attracting periodic orbits and the coexistence of all three species is enhanced as the competition between the IG prey and IG predator for the basal resource is close to the Hopf bifurcation curve from below. Our results indicate that the intraguild predation food web model exhibits rich and complex dynamic behaviors and strong Allee effect in the basal prey increases the extinction risk of not only the basal prey but also the IG prey or/and IG predator.  相似文献   

13.
In this paper, we present a stability analysis of a Lotka-Volterra commensal symbiosis model subject to Allee effect on the unaffected population which occurs at low population density. By analyzing the Jacobian matrix about the positive equilibrium, we show that the positive equilibrium is locally asymptotically stable. By applying the differential inequality theory, we show that the system is permanent, consequently, the boundary equilibria of the system is unstable. Finally, by using the Dulac criterion, we show that the positive equilibrium is globally stable. Although Allee effect has no influence on the final densities of the predator and prey species, numeric simulations show that the system subject to an Allee effect takes much longer time to reach its stable steady-state solution, in this sense that Allee effect has unstable effect on the system, however, such an effect is controllable. Such an finding is greatly different to that of the predator-prey model.  相似文献   

14.
15.
Motivated by models from evolutionary population dynamics, we study a general class of nonlinear difference equations called matrix models. Under the assumption that the projection matrix is non-negative and irreducible, we prove a theorem that establishes the global existence of a continuum with positive equilibria that bifurcates from an extinction equilibrium at a value of a model parameter at which the extinction equilibrium destabilizes. We give criteria for the global shape of the continuum, including local direction of bifurcation and its relationship to the local stability of the bifurcating positive equilibria. We discuss a relationship between backward bifurcations and Allee effects. Illustrative examples are given.  相似文献   

16.
In this paper, we consider a predator–prey model with herd behavior and prey‐taxis subject to the homogeneous Neumann boundary condition. First, by analyzing the characteristic equation, the local stability of the positive equilibrium is discussed. Then, choosing prey‐tactic sensitivity coefficient as the bifurcation parameter, we obtain a branch of nonconstant solutions bifurcating from the positive equilibrium by an abstract bifurcation theory, and find the stable bifurcating solutions near the bifurcation point under suitable conditions. We have shown that prey‐taxis can destabilize the uniform equilibrium and yields the occurrence of spatial patterns. Furthermore, some numerical simulations to illustrate the theoretical analysis are also carried out, Turing patterns such as spots pattern, spots–strip pattern, strip pattern, stable nonconstant steady‐state solutions, and spatially inhomogeneous periodic solutions are obtained, which also expand our theoretical results.  相似文献   

17.
In this article, we investigate the effect of prey refuge and time delay on a diffusive predator‐prey system with Holling II functional response and hyperbolic mortality subject to Neumann boundary condition. More precisely, we study Turing instability of positive equilibrium by using refuge as parameter, instability and Hopf bifurcation induced by time delay. In addition, by the theory of normal form and center manifold, we derive conditions for determining the bifurcation direction and the stability of the bifurcating periodic solution. © 2016 Wiley Periodicals, Inc. Complexity 21: 446–459, 2016  相似文献   

18.
In this paper, we investigate the complex dynamics induced by Allee effect in a predator–prey model. For the non-spatial model, Allee effect remains the boundedness of positive solutions, and it also induces the model to exhibit one or two positive equilibria. Especially, in the case with strong Allee effect, the model is bistable. For the spatial model, without Allee effect, there is the nonexistence of diffusion-driven instability. And in the case with Allee effect, the positive equilibrium can be unstable under certain conditions. This instability is induced by Allee effect and diffusion together. Furthermore, via numerical simulations, the model dynamics exhibits both Allee effect and diffusion controlled pattern formation growth to holes, stripe–hole mixtures, stripes, stripe–spot mixtures, and spots replication. That is to say, the dynamics of the model with Allee effect is not simple, but rich and complex.  相似文献   

19.
We study the local dynamics and supercritical Neimark‐Sacker bifurcation of a discrete‐time Nicholson‐Bailey host‐parasitoid model in the interior of . It is proved that if α>1, then the model has a unique positive equilibrium point , which is locally asymptotically focus, unstable focus and nonhyperbolic under certain parametric condition. Furthermore, it is proved that the model undergoes a supercritical Neimark‐Sacker bifurcation in a small neighborhood of the unique positive equilibrium point , and meanwhile, the stable closed curve appears. From the viewpoint of biology, the stable closed curve corresponds to the period or quasiperiodic oscillations between host and parasitoid populations. Some numerical simulations are presented to verify theoretical results.  相似文献   

20.
In this paper, the Allee effect is incorporated into a predator–prey model with Holling type II functional response. Compared with the predator–prey model without Allee effect, we find that the Allee effect of prey species increases the extinction risk of both predators and prey. When the handling time of predators is relatively short and the Allee effect of prey species becomes strong, both predators and prey may become extinct. Moreover, it is shown that the model with Allee effect undergoes the Hopf bifurcation and heteroclinic bifurcation. The Allee effect of prey species can lead to unstable periodical oscillation. It is also found that the positive equilibrium of the model could change from stable to unstable, and then to stable when the strength of Allee effect or the handling time of predators increases continuously from zero, that is, the model admits stability switches as a parameter changes. When the Allee effect of prey species becomes strong, longer handling time of predators may stabilize the coexistent steady state.  相似文献   

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