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1.
ABSTRACTA stage-structured predator–prey system with distributed maturation delay and harvesting is investigated. General birth and death functions are used. The local stability of each feasible equilibria is discussed. By using the persistence theory, it is proven that the system is permanent if the coexistence equilibrium exists. By using Lyapunov functional and LaSalle invariant principle, it is shown that the trivial equilibrium is globally stable when the other equilibria are not feasible, and that the boundary equilibrium is globally stable if the coexistence equilibrium does not exist. Finally, sufficient conditions are derived for the global stability of the coexistence equilibrium. 相似文献
2.
In this paper, a predator–prey system with harvesting prey and disease in prey species is given. In the absence of time delay, the existence and stability of all equilibria are investigated. In the presence of time delay, some sufficient conditions of the local stability of the positive equilibrium and the existence of Hopf bifurcation are obtained by analysing the corresponding characteristic equation, and the properties of Hopf bifurcation are given by using the normal form theory and centre manifold theorem. Furthermore, an optimal harvesting policy is investigated by applying the Pontryagin's Maximum Principle. Numerical simulations are performed to support our analytic results. 相似文献
4.
This paper deals with the problem of non-selective harvesting of a prey–predator system by using a reasonable catch-rate function instead of usual catch-per-unit-efforthypothesis. Here both the prey and the predator species obey the law of logistic growth. We have taken the predator functional response to prey density in such a form that each predator's functional response to the prey density approaches a constant as the prey population increases. Boundedness of the exploited system is examined. The existence of its steady states and their stability (local and global) are studied using Eigenvalue analysis. The existence of bionomic equilibria has been illustrated using a numerical example. The problem of determining the optimal harvesting policy is then solved by using Pontryagin's maximum principle. 相似文献
5.
Gauss's competitive exclusive principle states that two competing species having analogous environment cannot usually occupy the same space at a time but in order to exploit their common environment in a different manner, they can co-exist only when they are active in different times. On the other hand, several studies on predators in various natural and laboratory situations have shown that competitive coexistence can result from predation in a way by resisting any one prey species from becoming sufficiently abundant to outcompete other species such that the predator makes the coexistence possible. It has also been shown that the use of refuges by a fraction of the prey population exerts a stabilizing effect in the interacting population dynamics. Further, the field surveys in the Sundarban mangrove ecosystem reveal that two detritivorous fishes, viz. Liza parsia and Liza tade (prey population) coexist in nature with the presence of the predator fish population, viz. Lates calcarifer by using refuges. 相似文献
6.
We consider a modified Holling-type II predator–prey model, based on the premise that the search rate of predators is dependent on the prey density, rather than constant. A complete analysis of the global behavior of the model is presented, and shows that the model exhibits a dichotomy similar to the classical Holling-type II model: either the coexistence steady state is globally stable; or it is unstable, and then a unique, globally stable limit cycle exists. We discuss the similarities, but also important differences between our model and the Holling-type II model. The main differences are that: 1. The paradox of enrichment which always occurs in the Holling-type II model, does not always occur here, and 2. Even when the paradox of enrichment occurs, predators can adapt by lowering their search rate, and effectively stabilize the system. 相似文献
7.
Predation on a species subjected to an infectious disease can affect both the infection level and the population dynamics. There is an ongoing debate about the act of managing disease in natural populations through predation. Recent theoretical and empirical evidence shows that predation on infected populations can have both positive and negative influences on disease in prey populations. Here, we present a predator–prey system where the prey population is subjected to an infectious disease to explore the impact of predator on disease dynamics. Specifically, we investigate how the interference among predators affects the dynamics and structure of the predator–prey community. We perform a detailed numerical bifurcation analysis and find an unusually large variety of complex dynamics, such as, bistability, torus and chaos, in the presence of predators. We show that, depending on the strength of interference among predators, predators enhance or control disease outbreaks and population persistence. Moreover, the presence of multistable regimes makes the system very sensitive to perturbations and facilitates a number of regime shifts. Since, the habitat structure and the choice of predators deeply influence the interference among predators, thus before applying predators to control disease in prey populations or applying predator control strategy for wildlife management, it is essential to carefully investigate how these predators interact with each other in that specific habitat; otherwise it may lead to ecological disaster. 相似文献
8.
Group defense is a strategy widely employed by various species. We consider the effect of grouping on population persistence when animals join together in herds in order to provide a self-defense from predators. In literature, group defense is usually addressed in terms of individual behavioral responses. In this paper, we consider an alternative ‘mean-field’ approach which uses prey and predator densities as the dynamical variables. The model is essentially a predator–prey system but with an unconventional parametrization for the predation term. We discuss the outcomes of the ecosystem dynamics in terms of persistence and prey survival. In the spatially distributed model some specific spatio-temporal features are discovered. 相似文献
9.
In this paper, we propose a prey–predator system with stage structure for predator. The proposed system incorporates cannibalism for predator populations in a competitive environment. The combined fishing effort is considered as control used to harvest the populations. The steady states of the system are determined and the dynamical behavior of the system is discussed. Local stability of the system is analyzed and sufficient conditions are derived for the global stability of the system at the positive equilibrium point. The existence of the Hopf bifurcation phenomenon is examined at the positive equilibrium point of the proposed system. We consider harvesting effort as a control parameter and subsequently, characterize the optimal control parameter in order to formulate the optimal control problem under the dynamic framework towards optimal utilization of the resource. Moreover, the optimal system is solved numerically to investigate the sustainability of the ecosystem using an iterative method with a Runge–Kutta fourth-order scheme. Simulation results show that the optimal control scheme can achieve sustainable ecosystem. Results are analyzed with the help of graphical illustrations. 相似文献
10.
To understand the effect of the probability of a predator catching prey, Pcatch, on the stability of the predator–prey system, a spatially explicit lattice model consisting of predators, prey, and grass was constructed. The predators and prey randomly move on the lattice space, and the grass grows according to its growth probability. When a predator encounters prey, the predator eats the prey in accordance with the probability Pcatch. When a prey encounters grass, the prey eats the grass. The predator and prey give birth to offspring according to a birth probability after eating prey or grass, respectively. When a predator or prey is initially introduced or newly born, its health state is set at a high given value. This health state decreases by one with every time step. When the state of an animal decreases to less than zero, the individual dies and is removed from the system. Population densities for predator and prey fluctuated significantly according to Pcatch. System stability was characterized by the standard deviation ? of the fluctuation. The simulation results showed that ? for predators increased with an increase of Pcatch; ? for prey reached a maximum at Pcatch = 0.4; and ? for grass fluctuated little regardless of Pcatch. These results were due to the tradeoff between Pcatch and the predator–prey encounter rate, which represents the degree of interaction between predator and prey and the average population density, respectively. 相似文献
11.
We extend the aggregation model from Fetecau ( 2011) by adding a field of vision to individuals and by including a second species. The two species, assumed to have a predator–prey relationship, have dynamics governed by nonlocal kinetic equations that include advection and turning. The latter is the main mechanism for aggregation and orientation, which results from interactions among individuals of the same species as well as predator–prey relationships. We illustrate numerically a diverse set of predator–prey behaviors that can be captured by this model. We show that a prey’s escape outcome depends on the social interactions between its group members, the prey’s field of vision and the sophistication of the predator’s hunting strategies. 相似文献
12.
Many ecological systems show striking non-homogeneous population distributions. Diffusion-driven instabilities are commonly studied as mechanisms of pattern formation in many fields of biology but only rarely in ecology, in part because some of the conditions seem quite restrictive for ecological systems. Seasonal variation is ubiquitous in temperate ecosystems, yet its effect on pattern formation has not yet been explored. We formulate and analyze an impulsive reaction–diffusion system for a resource and its consumer in a two-season environment. While the resource grows throughout the ‘summer’ season, the consumer reproduces only once per year. We derive conditions for diffusion-driven instability in the system, and we show that pattern formation is possible with a Beddington–DeAngelis functional response. More importantly, we find that a low overwinter survival probability for the resource enhances the propensity for pattern formation: diffusion-driven instability occurs even when the diffusion rates of prey and predator are comparable (although not when they are equal). 相似文献
13.
We present a complete parametric analysis of stability properties and dynamic regimes of an ODE model in which the functional response is a function of the ratio of prey and predator abundances. We show the existence of eight qualitatively different types of system behaviors realized for various parameter values. In particular, there exist areas of coexistence (which may be steady or oscillating), areas in which both populations become extinct, and areas of "conditional coexistence" depending on the initial values. One of the main mathematical features of ratio-dependent models, distinguishing this class from other predator-prey models, is that the Origin is a complicated equilibrium point, whose characteristics crucially determine the main properties of the model. This is the first demonstration of this phenomenon in an ecological model. The model is investigated with methods of the qualitative theory of ODEs and the theory of bifurcations. The biological relevance of the mathematical results is discussed both regarding conservation issues (for which coexistence is desired) and biological control (for which extinction is desired). 相似文献
14.
In this paper a Gause type model of interactions between predator and prey population is considered. We deal with the sufficient condition due to Kuang and Freedman in the generalized form including a kind of weight function. In a previous paper we proved that the existence of such weight function implies the uniqueness of limit cycle. In the present paper we give a new condition equivalent to the existence of a weight function (Theorem 4.4). As a consequence of our result, it is shown that some simple qualitative properties of the trophic function and the prey isocline ensure the uniqueness of limit cycle. 相似文献
15.
A refuge model is developed for a single predator species and either one or two prey species where no predators are present in the prey refuge. An individual’s fitness depends on its strategy choice or ecotype (predators decide which prey species to pursue and prey decide what proportion of their time to spend in the refuge) as well as on the population sizes of all three species. It is shown that, when there is a single prey species with a refuge or two prey species with no refuge compete only indirectly (i.e. there is only apparent competition between prey species), that stable resident systems where all individuals in each species have the same ecotype cannot be destabilized by the introduction of mutant ecotypes that are initially selectively neutral. In game-theoretic terms, this means that stable monomorphic resident systems, with ecotypes given by a Nash equilibrium, are both ecologically and evolutionarily stable. However, we show that this is no longer the case when the two indirectly-competing prey species have a refuge. This illustrates theoretically that two ecological factors, that are separately stabilizing (apparent competition and refuge use), may have a combined destabilizing effect from the evolutionary perspective. These results generalize the concept of an evolutionarily stable strategy (ESS) to models in evolutionary ecology. Several biological examples of predator–prey systems are discussed from this perspective. 相似文献
16.
This paper investigates complex dynamics of a predator–prey interaction model that incorporates: (a) an Allee effect in prey; (b) the Michaelis–Menten type functional response between prey and predator; and (c) diffusion in both prey and predator. We provide rigorous mathematical results of the proposed model including: (1) the stability of non-negative constant steady states; (2) sufficient conditions that lead to Hopf/Turing bifurcations; (3) a prior estimates of positive steady states; (4) the non-existence and existence of non-constant positive steady states when the model is under zero-flux boundary condition. We also perform completed analysis of the corresponding ODE model to obtain a better understanding on effects of diffusion on the stability. Our analytical results show that the small values of the ratio of the prey's diffusion rate to the predator's diffusion rate are more likely to destabilize the system, thus generate Hopf-bifurcation and Turing instability that can lead to different spatial patterns. Through numerical simulations, we observe that our model, with or without Allee effect, can exhibit extremely rich pattern formations that include but not limit to strips, spotted patterns, symmetric patterns. In addition, the strength of Allee effects also plays an important role in generating distinct spatial patterns. 相似文献
17.
An excitable model of fast phytoplankton and slow zooplankton dynamics is considered for the case of lysogenic viral infection of the phytoplankton population. The phytoplankton population is split into a susceptible ( S) and an infected ( I) part. Both parts grow logistically, limited by a common carrying capacity. Zooplankton ( Z) is grazing on susceptibles and infected, following a Holling-type III functional response. The local analysis of the S– I– Z differential equations yields a number of stationary and/or oscillatory regimes and their combinations. Correspondingly interesting is the behaviour under multiplicative noise, modelled by stochastic differential equations. The external noise can enhance the survival of susceptibles and infected, respectively, that would go extinct in a deterministic environment. In the parameter range of excitability, noise can induce prey–predator oscillations and coherence resonance (CR). In the spatially extended case, synchronized global oscillations can be observed for medium noise intensities. Higher values of noise give rise to the formation of stationary spatial patterns. 相似文献
18.
The existence and implications of alternative stable states in ecological systems have been investigated extensively within
deterministic models. However, it is known that natural systems are undeniably subject to random fluctuations, arising from
either environmental variability or internal effects. Thus, in this paper, we study the role of noise on the pattern formation
of a spatial predator–prey model with Allee effect. The obtained results show that the spatially extended system exhibits
rich dynamic behavior. More specifically, the stationary pattern can be induced to be a stable target wave when the noise
intensity is small. As the noise intensity is increased, patchy invasion emerges. These results indicate that the dynamic
behavior of predator–prey models may be partly due to stochastic factors instead of deterministic factors, which may also
help us to understand the effects arising from the undeniable susceptibility to random fluctuations of real ecosystems. 相似文献
19.
Use of additional/alternative food source to predators is one of the widely recognised practices in the field of biological control. Both theoretical and experimental works point out that quality and quantity of additional food play a vital role in the controllability of the pest. Theoretical studies carried out previously in this direction indicate that incorporating mutual interference between predators can stabilise the system. Experimental evidence also point out that mutual interference between predators can affect the outcome of the biological control programs. In this article dynamics of additional food provided predator–prey system in the presence of mutual interference between predators has been studied. The mutual interference between predators is modelled using Beddington–DeAngelis type functional response. The system analysis highlights the role of mutual interference on the success of biological control programs when predators are provided with additional food. The model results indicate the possibility of stable coexistence of predators with low prey population levels. This is in contrast to classical predator–prey models wherein this stable co-existence at low prey population levels is not possible. This study classifies the characteristics of biological control agents and additional food (of suitable quality and quantity), permitting the eco-managers to enhance the success rate of biological control programs. 相似文献
20.
The present study deals with the analysis of a predator–prey like model consisting of system of differential equations with piecewise constant arguments. A solution of the system with piecewise constant arguments leads to a system of difference equations which is examined to study boundedness, local and global asymptotic behaviour of the positive solutions. Using Schur–Cohn criterion and a Lyapunov function, we derive sufficient conditions under which the positive equilibrium point is local and global asymptotically stable. Moreover, we show numerically that periodic solutions arise as a consequence of Neimark-Sacker bifurcation of a limit cycle. 相似文献
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