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Dynamic behaviors of Lotka–Volterra predator–prey model incorporating predator cannibalism
Advances in Difference Equations volume 2019, Article number: 359 (2019)
Abstract
A Lotka–Volterra predator–prey model incorporating predator cannibalism is proposed and studied in this paper. The existence and stability of all possible equilibria of the system are investigated. Our study shows that cannibalism has both positive and negative effect on the stability of the system, it depends on the dynamic behaviors of the original system. If the predator species in the system without cannibalism is extinct, then suitable cannibalism may lead to the coexistence of both species, in this case, cannibalism stabilizes the system. If the cannibalism rate is large enough, the prey species maybe driven to extinction, while the predator species are permanent. If the two species coexist in the stable state in the original system, then predator cannibalism may lead to the extinction of the prey species. In this case, cannibalism has an unstable effect. Numeric simulations support our findings.
1 Introduction
The aim of this paper is to investigate the dynamic behaviors of the following predator–prey model with cannibalism for predator:
where \(c_{1}< c\), x and y are the density of the prey and predator at time t, respectively. b and α denote the intrinsic growth rate and intraspecific competition of the prey, respectively; β is the death rate of the predator; m denotes the strength of intraspecific interaction between prey and predator; n is the conversion efficiency of ingested prey into new predators; \(cy^{2}/(y+d)\) denotes the cannibalism of the predator; \(c_{1}\) is the birth rate from the predator cannibalism. All the coefficients are nonnegative constants.
As was pointed out by Berryman [1], the dynamic relationship between predator and prey has long been and will continue to be one of the dominant themes in both ecology and mathematical ecology due to its universal existence and importance. During the last decade, many scholars investigated the dynamic behaviors of the predator–prey species, see [2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40] and the references therein.
The traditional two species Lotka–Volterra predator–prey model takes the form
For the dynamic behaviors of (1.2), we summarize it as follows [6, 11].
Theorem A
In system (1.2), there are two boundary equilibria \(O(0,0)\), \(E^{1}( \frac{b}{\alpha }, 0) \). \(O(0,0)\) is a saddle and \(E^{1}( \frac{b}{\alpha }, 0)\) is globally asymptotically stable if \(\beta > \frac{bn}{\alpha }\). Assume that \(\beta < \frac{bn}{\alpha }\), the positive equilibrium \(E^{2} ( \frac{\beta }{n}, \frac{bn\alpha \beta }{mn} )\) exists, which is globally asymptotically stable.
In researching the dynamic behaviors of the predator–prey model, some scholars [2, 10,11,12, 17,18,19,20] considered the impact of the functional response for the predator–prey. For example, Yu [18] studied the global asymptotic stability of a predator–prey model with modified Leslie–Gower and Hollingtype II schemes:
where \(x(t)\), \(y(t)\) stand for the population (the density) of the prey and the predator at time t, respectively. Yu [18] provided two sets of sufficient conditions on the global asymptotic stability of a positive equilibrium. After that, Yue [19] considered the dynamics of a modified Leslie–Gower predator–prey model with Hollingtype II schemes and a prey refuge:
where mx is part of the refuge protecting of the prey, here \(m\in [0, 1)\). Yue [19] found that increasing the amount of refuge can ensure the coexistence and attractivity of the two species more easily.
In recent years, cannibalism as a special phenomenon in nature which often occurs in plankton [22], fishes [23], spiders [24], and social insect populations [26] attracted the attention of many scholars. It is a behavior that consumes the same species and helps to provide food sources. Obviously, cannibalism has a very important effect on the dynamic behaviors of the populations (see [22,23,24,25,26,27,28,29,30,31]).
Gao [25], Kang et al. [26], and RodriguezRodriguez et al. [27] proposed and studied the single species stagestructure model with cannibalism. Kang et al. [26] and RodriguezRodriguez et al. [27] thought cannibalism had a great significance for evolution. Zhang et al. [28] obtained a set of sufficient conditions for the permanence of the nonautonomous predator–prey system with periodic attacking rate. Recently, Zhang et al. [29] proposed the following stagestructure prey–predator model with cannibalism for predator:
where \(x(t)\) and \(y(t)\) are the densities of the adult predator and juvenile predator at time t, respectively, \(z(t)\) is the density of the prey at time t. The term \(\beta xy\) reflecting the intraspecific interaction denotes the cannibalization rate of adult predators to juvenile ones, the term \(\varepsilon xy \) is the rate of the adult predators increase due to being better fed through eating juveniles. Zhang et al. [29] obtained that large cannibalization rate can make the positive equilibrium globally stable although its stability would change with the increase of the cannibalism rate.
Generally speaking, scholars [22,23,24,25,26,27,28,29] used the bilinear function \(\beta x y\) to describe the cannibalism phenomenon. Only recently did scholars [30, 31] adopted the idea of the functional response of predator–prey model and proposed the nonlinear cannibalism model.
In 2016, Basheer et al. [30] proposed the prey–predator model with prey nonlinear cannibalism as follows:
where \(c_{1}< c\), u and v represent the densities of prey and predator at time t, respectively. The parameters \(c_{1}\), α, c, d, δ, and β are nonnegative constants. Different from the previous works [24,25,26,27,28,29], Basheer et al. [30] used the Holling II type functional response to describe cannibalism. Here the generic cannibalism term \(C(u)\) is added in the prey equation and is given by
where c is the cannibalism rate. This term is obviously more appropriate with the reality of ecology and has a clear gain of energy to the cannibalistic prey. This gain results in an increase in reproduction in the prey, modeled via adding a \(c_{1}u\) term to the prey equation. Obviously, \(c_{1}< c\), as it takes depredation of a number of prey by the cannibal to produce one new offspring. They obtained that prey cannibalism alters the dynamics of the predator–prey model. System (1.6) is stable with no cannibalism, while it is unstable with prey cannibalism under the same conditions. After that, Basheer et al. [31] studied the predator–prey model with cannibalism in both predator and prey population and obtained more detailed results.
As far as system (1.2) is concerned, if the boundary equilibrium point \(E^{1}\) of system (1.2) is globally asymptotically stable, which means that the predator will eventually become extinct and the prey will survive, then how does cannibalism affect the dynamic behaviors of the system? If the positive equilibrium point \(E^{2}\) of system (1.2) is globally asymptotically stable, then how does cannibalism affect the dynamic behaviors of the system? This motivated us to propose and study system (1.1).
The paper is arranged as follows. In the next section, we investigate the existence and local stability of the equilibria of system (1.1). In Sect. 3, we discuss the global stability of the equilibria. Numeric simulations are presented in Sect. 4 to show the feasibility of the main results. We end this paper with a brief discussion.
2 Existence and local stability of equilibria
In this paper, let \((x(t), y(t))\) be a solution of system (1.1) which satisfies the initial value \(x(0)>0\), \(y(0)>0 \), and we are only interested in the dynamics of system (1.1) in the first quadrant
2.1 The existence of equilibria
The equilibria of system (1.1) are determined by the system
The system always admits the boundary equilibria \(E_{0}(0,0)\), \(E_{1}( b/\alpha ,0)\), while for other possible boundary equilibria and positive equilibria, we need to consider the following cases:
(i) If \(x=0\), \(y\neq0\), we may have the other boundary equilibrium \(E_{2}(0,y_{1})\), where \(y_{1}\) is the root of the following equation:
After simplifying calculation, we can get \(y= \frac{d(c_{1}\beta )}{\beta +cc_{1}}\). The boundary equilibrium \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) exists if \(c_{1}>\beta \).
(ii) If \(x\neq0\), \(y\neq0\), the interior equilibrium \(E^{*}(x^{*},y^{*})\) is determined by the equations as follows:
From the first equation of (2.3), we have \(y= \frac{b\alpha x}{m}\). Substituting y into the second equation of (2.3), we can get the equation as follows:
where \(A=\alpha n\), \(B=\alpha (\beta +cc_{1})+bn+dmn\), \(C=b(\beta +cc_{1})+dm(\beta c_{1})\). Obviously, \(A>0\), \(B>0\). Let Δ denote the discriminant of Eq. (2.4) and express it as follows:
From \(y= \frac{b\alpha x}{m}>0\), we have
Now, we will discuss the root of Eq. (2.4) under the assumption that inequality (2.6) holds.

(a)
If \(C\leq 0\), Eq. (2.4) has the unique positive root \(x_{1}= \frac{B+\sqrt{B^{2}4AC}}{2A}\geq \frac{B}{A}> \frac{b}{\alpha }\). Obviously, \(x_{1}\) does not satisfy the condition of (2.6).

(b)
If \(C>0\), we have \(\beta > c_{1}\) or \(\beta \leq c_{1}< \beta +\frac{bc}{b+dm}\). Then Eq. (2.4) has two positive roots \(x_{2,3}= \frac{B\pm \sqrt{B^{2}4AC}}{2A}\).
Defining the function \(f(x)=Ax^{2}Bx+C\), we have
(1) If \(\beta \leq c_{1}<\beta + \frac{bc}{b+dm}\), we have \(f( \frac{b}{\alpha })<0\), then system (1.1) has a positive equilibrium \(E_{3}(x_{2}^{*}, y_{2}^{*})\), where \(x_{2}^{*}= \frac{B\sqrt{B^{2}4AC}}{2A}\), \(y_{2}^{*}= \frac{b\alpha x_{2}^{*}}{m}\).
(2) If \(\beta > c_{1}\), we cannot determine the size of \(f( \frac{b}{\alpha })\). So we will discuss the following:
If \(f( \frac{b}{\alpha })<0\), we have
it is similar to case (1).
If \(f( \frac{b}{\alpha })\geq 0\), we have
Consider \(x_{3}\leq \frac{b}{\alpha }\), after simplifying calculation, we have
Obviously, it contradicts with (2.9). So system (1.1) has no positive equilibrium.
Summarizing the above discussion, we obtain the following theorem.
Theorem 2.1
For all positive parameters, there are two boundary equilibria \(E_{0}(0, 0)\), \(E_{1}( \frac{b}{\alpha }, 0)\). The boundary equilibrium \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) exists if \(c_{1}>\beta \). In system (1.1), for the positive equilibrium, we have:

(i)
If \(0<\beta c_{1}< \frac{bn}{\alpha }\), then system (1.1) has the unique positive equilibrium \(E^{*}(x_{2}^{*}, y_{2}^{*})\), where \(x_{2}^{*}= \frac{B\sqrt{B^{2}4AC}}{2A}\), \(y_{2}^{*}= \frac{b\alpha x_{2}^{*}}{m}\).

(ii)
If \(\beta \leq c_{1}<\beta + \frac{bc}{b+dm}\), then system (1.1) has the unique positive equilibrium \(E^{*}(x_{2}^{*}, y_{2}^{*})\), where \(x_{2}^{*}= \frac{B\sqrt{B^{2}4AC}}{2A}\), \(y_{2}^{*}= \frac{b\alpha x_{2}^{*}}{m}\).
2.2 The local stability of equilibria
Theorem 2.2
In system (1.1), for the boundary equilibrium \(E_{0}(0,0)\), we have

(1)
If \(c_{1}<\beta \), then \(E_{0}(0, 0)\) is a saddle;

(2)
If \(c_{1}=\beta \), then \(E_{0}(0, 0)\) is a saddle node;

(3)
If \(c_{1}>\beta \), then \(E_{0}(0, 0)\) is an unstable node.
Proof
The Jacobian matrix of system (1.1) is calculated as follows:
Then the Jacobian matrix of system (1.1) about the equilibrium \(E_{0}(0,0)\) is
The eigenvalues of \(J(E_{0})\) are \(\lambda _{1}=b>0\), \(\lambda _{2}=c _{1}\beta \). Hence, if \(\lambda _{2}=c_{1}\beta <0\), i.e., \(\beta >c_{1}\), then \(E_{0}(0, 0)\) is a saddle. If \(\lambda _{2}=c_{1} \beta >0\), i.e., \(\beta < c_{1}\), then we have
so \(E_{0}(0,0)\) is an unstable node. If \(\lambda _{2}=c_{1}\beta =0\), namely \(\beta =c_{1}\), the eigenvalues are now given by \(\lambda _{1}=b>0\), \(\lambda _{2}=0\). Then Theorem 7.1 in Chap. 2 in [32] is used to determine the stability of the equilibrium \(E_{0}\). Let \(d\tau =bdt\), where τ is a new time variable, which makes the system into the following form:
where \(Q_{1}(x,y)\) is a power series in \((x,y)\) with terms \(x^{i}y ^{j}\) satisfying \(i+j\ge 4\).
By the implicit function theorem, there is a unique function \(x=\phi (y)\) in the first quadrant such that \(\phi (0)=0\) near the origin. From \(\frac{dx}{d\tau }=0 \), we get the implicit function \(x=0\), then
According to Theorem 7.1 in Chap. 2 in [32], we have \(m=2\), \(a_{m}= \frac{c}{bd}>0\), so \(E_{0}(0, 0)\) is a saddle node.
The proof of Theorem 2.2 is finished. □
Theorem 2.3
In system (1.1), for the boundary equilibrium \(E_{1}( \frac{b}{\alpha }, 0)\), we have:

(1)
If \(c_{1}\geq \beta \), then \(E_{1}( \frac{b}{\alpha }, 0)\) is a saddle;

(2)
If \(c_{1}<\beta \), then:

(i)
If \(\beta c_{1}< \frac{bn}{\alpha }\), then \(E_{1}( \frac{b}{\alpha }, 0)\) is a saddle;

(ii)
If \(\beta c_{1}> \frac{bn}{\alpha }\), then \(E_{1}( \frac{b}{\alpha }, 0)\) is a stable node;

(iii)
If \(\beta c_{1}= \frac{bn}{\alpha }\), then \(E_{1}( \frac{b}{\alpha }, 0)\) is a saddle node.

(i)
Proof
The Jacobian matrix of system (1.1) about the equilibrium \(E_{1}( \frac{b}{\alpha }, 0)\) is given by
The eigenvalues of \(J(E_{1})\) are \(\lambda _{1}=b<0\), \(\lambda _{2}= \frac{bn}{\alpha }(\beta c_{1})\).
If \(\beta c_{1}\leq 0\), i.e., \(c_{1}\geq \beta \), then \(\lambda _{2}= \frac{bn}{\alpha }(\beta c_{1})>0\), so \(E_{1}( \frac{b}{\alpha }, 0)\) is a saddle.
If \(c_{1}<\beta \), we have \(\lambda _{2}>0\), if \(\frac{bn}{\alpha }>\beta c_{1}\), then \(E_{1}( \frac{b}{\alpha }, 0)\) is a saddle.
If \(c_{1}<\beta \) and \(\frac{bn}{\alpha }<\beta c_{1}\), then \(\lambda _{2}<0\), we have
so \(E_{1}( \frac{b}{\alpha }, 0)\) is a stable node.
If \(c_{1}<\beta \) and \(\frac{bn}{\alpha }=\beta c_{1}\), then \(\lambda _{2}=0\), the eigenvalues are now given by \(\lambda _{1}=b<0\), \(\lambda _{2}=0\). Then Theorem 7.1 in Chap. 2 in [32] is used to determine the stability of the equilibrium \(E_{1}\). Now we transform the equilibrium \(E_{1}\) to the origin by translation \((X,Y)=(x \frac{b}{\alpha },y)\) at first, and then expand in power series up to the forth order around the origin, which makes the system into the following form:
where \(Q_{2}(X,Y)\) is a power series in \((X,Y)\) with terms \(X^{i}Y ^{j}\) satisfying \(i+j\ge 5\).
Let \(x=bX \frac{bm}{\alpha }Y\), \(y=Y\), \(d\tau =bdt\), where τ is a new time variable, then we have
where \(P_{1}(x,y)\) and \(Q_{3}(x,y)\) are the power series in \((x,y)\) with terms \(x^{i}y^{j}\) satisfying \(i+j\ge 4\).
By the implicit function theorem, there is a unique function \(x=\phi (y)\) in the first quadrant such that \(\phi (0)=0\) near the origin. From \(\frac{dx}{d\tau }=0 \), we could obtain the implicit function \(x= \frac{m}{\alpha }( \frac{mn}{\alpha }+ \frac{c}{d})y^{2}+P_{2}(x, y)\), then
where \(P_{2}(x, y)\) and \(Q_{4}(x, y)\) are the power series in \((x, y)\) with terms \(x^{i}y^{j}\) satisfying \(i+j\ge 3\).
According to Theorem 7.1 in Chap. 2 in [32], we have \(m=2\), \(a_{m}= \frac{mn}{b\alpha }+ \frac{c}{bd}>0\), so \(E_{1}( \frac{b}{\alpha }, 0)\) is a saddle node.
The proof of Theorem 2.3 is finished. □
Theorem 2.4
In system (1.1), when the boundary equilibrium \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) exists, we have

(1)
If \(\beta < c_{1}<\beta + \frac{b(\beta +c)+\beta dm}{b+dm}\), then \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) is a saddle;

(2)
If \(c_{1}>\beta + \frac{b(\beta +c)+\beta dm}{b+dm}\), then \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) is a stable node;

(3)
If \(c_{1}=\beta + \frac{b(\beta +c)+\beta dm}{b+dm}\), then \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) is a saddle node.
Proof
The Jacobian matrix of system (1.1) about the equilibrium \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) is
The eigenvalues of \(J(E_{2})\) are \(\lambda _{1}= \frac{C}{c+\beta c_{1}}\), \(\lambda _{2}= \frac{cdy_{2}}{(y+d)^{2}}<0\).
If \(C>0\), i.e., \(\beta < c_{1}<\beta + \frac{b(\beta +c)+\beta dm}{b+dm}\), we have \(\lambda _{1}= \frac{C}{c+\beta c_{1}}>0\), so \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) is a saddle.
If \(c_{1}>\beta + \frac{b(\beta +c)+\beta dm}{b+dm}\), then we have
so \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) is a stable node.
If \(c_{1}=\beta + \frac{b(\beta +c)+\beta dm}{b+dm}\), then \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) is a saddle node. The proof is similar to Theorem 2.3, we omitted it.
The proof of Theorem 2.4 is finished. □
Theorem 2.5
In system (1.1), when the equilibrium \(E^{*}(x^{*}, y^{*})\) exists, it is locally asymptotically stable.
Proof
The Jacobian matrix of system (1.1) about the equilibrium \(E^{*}(x^{*}, y^{*})\) is
Then we have
and
So \(E^{*}(x^{*}, y^{*})\) is locally asymptotically stable.
The proof of Theorem 2.5 is finished. □
3 Global stability of equilibria
In this section we consider the global asymptotic stability of the equilibria.
Theorem 3.1
Assume that
holds, then \(E_{1}(\frac{b}{\alpha }, 0)\) is globally asymptotically stable.
Proof
We will prove Theorem 3.1 by constructing some suitable Lyapunov function.
Let us define a Lyapunov function
where \(\overline{x}=\frac{b}{\alpha }\). Then the time derivative of \(V_{1}\) along the trajectories of (1.1) is
Thus, \(V_{1}(x, y)\) satisfies Lyapunov asymptotic stability theorem, and the boundary equilibrium \(E_{1}( \frac{b}{\alpha }, 0)\) of system (1.1) is globally asymptotically stable.
The proof of Theorem 3.1 is finished. □
Theorem 3.2
Assume that
holds, then \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) is globally asymptotically stable.
Proof
We will prove Theorem 3.2 by constructing some suitable Lyapunov function.
Let us define a Lyapunov function
where \(\overline{y}= \frac{d(c_{1}\beta )}{\beta +cc_{1}}\). Then the time derivative of \(V_{2}\) along the trajectories of (1.1) is
Thus, \(V_{2}(x, y)\) satisfies Lyapunov asymptotic stability theorem, and the boundary equilibrium \(E_{2} (0, \frac{d(c_{1}\beta )}{\beta +cc_{1}} )\) of system (1.1) is globally asymptotically stable.
The proof of Theorem 3.2 is finished. □
Theorem 3.3
When the equilibrium \(E_{3}(x^{*}, y^{*})\) exists, it is globally asymptotically stable.
Proof
We will prove Theorem 3.3 by constructing some suitable Lyapunov functions.
Let us define a Lyapunov function
Then the time derivative of \(V_{3}\) along the trajectories of (1.1) is
Thus, \(V_{3}(x, y)\) satisfies Lyapunov asymptotic stability theorem, and the positive equilibrium \(E_{3}(x^{*}, y^{*})\) of system (1.1) is globally asymptotically stable when the equilibrium \(E_{3}(x^{*}, y ^{*})\) exists.
The proof of Theorem 3.3 is finished. □
4 Numerical simulations
In this section we consider the dynamics of systems (1.1) and (1.2) under different parameters.
Let \(b=5\), \(\alpha =3\), \(m=0.6\), \(\beta =2.5\), \(n=1.2\), then system (1.2) is given by
We have \(\frac{bn}{\alpha }=2<\beta =2.5\). From Theorem A, system (4.1) has two boundary equilibria \(O(0,0)\), \(E^{1}(1.67, 0)\), and \(E_{0}(0,0)\) is a saddle, \(E^{1}(1.67, 0)\) is globally asymptotically stable (see Fig. 1).
Now we consider some cannibalism parameters on the basis of (4.1). Let \(c=8\), \(d=15\), then system (1.1) is given by
We consider \(c_{1}\) as variable. System (4.2) always has two boundary equilibria \(E_{0}(0,0)\), \(E_{1}(1.67, 0)\) from Theorem 2.1. If \(c_{1}=0.4\), from Sect. 2.2, we have \(E_{0}(0,0)\) is a saddle and \(E_{1}(1.67, 0)\) is a stable node (see Fig. 2). If \(c_{1}=2\), the positive equilibrium \(E^{*}(1.26, 2.11)\) exists, which is globally asymptotically stable. \(E_{0}(0, 0)\) and \(E_{1}(1.67, 0)\) are saddle (see Fig. 3). If \(c_{1}=2.5\), system (4.2) has a globally asymptotically stable positive equilibrium \(E^{*}(1.1, 2.97)\), \(E_{0}(0,0)\) is a saddle node, \(E_{1}(1.67, 0)\) is a saddle (see Fig. 4). If \(c_{1}=5\), system (4.2) has a boundary equilibrium \(E_{2}(0, 6.9)\), which is a saddle. Then \(E_{0}(0, 0)\) is an unstable node, \(E_{1}(1.67, 0)\) is a saddle, \(E^{*}(0.163, 7.63)\) is globally asymptotically stable (see Fig. 5). If \(c_{1}=7.86\), the positive equilibria of system (4.2) will disappear, and the boundary equilibrium \(E_{1}(0, 30.4)\) is globally asymptotically stable. \(E_{0}(0, 0)\) is an unstable node, \(E_{1}(1.67, 0)\) is a saddle (see Fig. 6).
Now let us consider system (1.2), which has a unique positive equilibrium, let \(b=5\), \(\alpha =3\), \(m=0.6\), \(\beta =2.5\), \(n=1.8\), then system (1.2) is
We have \(\frac{bn}{\alpha }=3>\beta =2.5\). From Theorem A, system (4.3) has two boundary equilibria \(O(0,0)\), \(E^{1}(1.67, 0)\) and a unique positive equilibrium \(E^{2}(1.39, 1.36)\), and \(E_{0}(0,0)\) is a saddle, \(E^{1}(1.67, 0)\) is unstable, and \(E^{2}(1.39, 1.36)\) is globally asymptotically stable (see Fig. 7).
We consider the predator cannibalism based on system (4.3). Let \(c=8\), \(d=15\), then we have
System (4.4) always has two boundary equilibria \(E_{0}(0,0)\), \(E_{1}(1.67, 0)\) from Theorem 2.1. If \(c_{1}=2\), the positive equilibrium \(E^{*}(1.05, 3.12)\) exists, which is globally asymptotically stable. \(E_{0}(0, 0)\) and \(E_{1}(1.67, 0)\) are saddle (see Fig. 8). If \(c_{1}=5\), system (4.4) has a boundary equilibrium \(E_{2}(0, 6.87)\), which is a saddle. Then \(E_{0}(0, 0)\) is an unstable node, \(E_{1}(1.67, 0)\) is a saddle, \(E^{*}(0.139, 7.84)\) is globally asymptotically stable (see Fig. 9). If \(c_{1}=7.86\), the positive equilibrium will disappear for system (4.4), and the boundary equilibrium \(E_{1}(0, 30.6)\) is globally asymptotically stable. \(E_{0}(0, 0)\) is an unstable node, \(E_{1}(1.67, 0)\) is a saddle (see Fig. 10).
5 Conclusion
Based on the traditional Lotka–Volterra predator–prey model, we propose and study a predator–prey model with predator cannibalism in this paper. We have investigated the local and global stability of the possible equilibria of the model. Meanwhile, we can find some interesting phenomenon about the dynamic behaviors of system (1.1). If system (1.2) (no cannibalism, i.e., \(c=0\) and \(c_{1}=0\)) has a boundary equilibrium \(E^{1}( \frac{b}{\alpha }, 0)\), which is globally asymptotically stable (see Fig. 1), a suitable cannibalism rate (\((\beta < c_{1}<\beta + \frac{b(\beta +c)+\beta dm}{b+dm} )\)) leads to system (1.1) admitting a unique positive equilibrium, and it is globally asymptotically stable (see Fig. 3, Fig. 4, and Fig. 5). That is to say, cannibalism within a certain range can make the two species persistent. So in this case, cannibalism in a certain range has a positive effect for the coexistence of the prey and the predator. With the increase of \(c_{1}\), the positive equilibrium will disappear and the boundary equilibrium \(E_{2} (0, \frac{d(c_{1}\beta )}{c+\beta c_{1}} )\) will appear (see Fig. 6). That is to say, without other sources of food, predator populations can still survive on cannibalism. For example, salamanders only depend on cannibalism to survive in summer.
If system (1.2) has a positive equilibrium \(E^{2}( \frac{\beta }{n}, \frac{bm\alpha \beta }{mn})\), which is globally asymptotically stable (see Fig. 7), with the increase of \(c_{1}\), the population density of prey decreases while that of predator increases (see Fig. 8 and Fig. 9). When \(c_{1}\) is large enough, prey populations will be driven to extinction. That is to say, predator cannibalism will make prey extinct (see Fig. 10). Predator cannibalism also changes the type of the equilibria (see Fig. 1, Fig. 5, and Fig. 6; Fig. 7, Fig. 9, and Fig. 10).
That is, by introducing the predator cannibalism, the dynamic behaviors of the system become complicated.
References
Berryman, A.A.: The origins and evolution of predator–prey theory. Ecology 73(5), 1530–1535 (1992)
Chen, F., Chen, L., Xie, X.: On a Leslie–Gower predator–prey model incorporating a prey refuge. Nonlinear Anal., Real World Appl. 10(5), 2905–2908 (2009)
Chen, F., Wang, H., Lin, Y., et al.: Global stability of a stagestructured predator–prey system. Appl. Math. Comput. 223, 45–53 (2013)
Chen, L., Chen, F., Chen, L.: Qualitative analysis of a predator–prey model with Holling type II functional response incorporating a constant prey refuge. Nonlinear Anal., Real World Appl. 11(1), 246–252 (2010)
Chen, F., Ma, Z., Zhang, H.: Global asymptotical stability of the positive equilibrium of the Lotka–Volterra prey–predator model incorporating a constant number of prey refuges. Nonlinear Anal., Real World Appl. 13(6), 2790–2793 (2012)
Li, Z., Chen, F., He, M.: Permanence and global attractivity of a periodic predator–prey system with mutual interference and impulses. Commun. Nonlinear Sci. Numer. Simul. 17(1), 444–453 (2012)
Li, Z., Han, M., Chen, F.: Global stability of a stagestructured predator–prey model with modified Leslie–Gower and Hollingtype II schemes. Int. J. Biomath. 5(06), 1250057 (2012)
Li, Z., Han, M., Chen, F.: Global stability of a predator–prey system with stage structure and mutual interference. Discrete Contin. Dyn. Syst., Ser. B 19(1), 173–187 (2014)
Ma, Z., Chen, F., et al.: Dynamic behaviors of a Lotka–Volterra predator–prey model incorporating a prey refuge and predator mutual interference. Appl. Math. Comput. 219(15), 7945–7953 (2013)
Xiao, Z., Li, Z., Zhu, Z., et al.: Hopf bifurcation and stability in a Beddington–DeAngelis predator–prey model with stage structure for predator and time delay incorporating prey refuge. Open Math. 17(1), 141–159 (2019)
Zhang, N., Chen, F., Su, Q., et al.: Dynamic behaviors of a harvesting Leslie–Gower predator–prey model. Discrete Dyn. Nat. Soc. 2011, Article ID 473949 (2011)
Xie, X., Xue, Y., Chen, J., et al.: Permanence and global attractivity of a nonautonomous modified Leslie–Gower predator–prey model with Hollingtype II schemes and a prey refuge. Adv. Differ. Equ. 2016(1), 184 (2016)
Lin, Y., Xie, X., et al.: Convergences of a stagestructured predator–prey model with modified Leslie–Gower and Hollingtype II schemes. Adv. Differ. Equ. 2016(1), 181 (2016)
Yang, L., Xie, X., et al.: Permanence of the periodic predator–preymutualist system. Adv. Differ. Equ. 2015(1), 331 (2015)
Guan, X., Liu, Y., Xie, X.: Stability analysis of a Lotka–Volterra type predator–prey system with Allee effect on the predator species. Commun. Math. Biol. Neurosci. 2018, Article ID 9 (2018)
Lin, Q.: Note on the stability property of a ratiodependent Holling–Tanner model. Commun. Math. Biol. Neurosci. 2019, Article ID 10 (2019)
Yu, S.: Global stability of a modified Leslie–Gower model with Beddington–DeAngelis functional response. Adv. Differ. Equ. 2014(1), 84 (2014)
Yu, S.: Global asymptotic stability of a predator–prey model with modified Leslie–Gower and Hollingtype II schemes. Discrete Dyn. Nat. Soc. 2012, Article ID 208167 (2012)
Yue, Q.: Dynamics of a modified Leslie–Gower predator–prey model with Hollingtype II schemes and a prey refuge. SpringerPlus 5(1), 461 (2016)
Yue, Q.: Permanence for a modified Leslie–Gower predator–prey model with Beddington–DeAngelis functional response and feedback controls. Adv. Differ. Equ. 2015(1), 81 (2015)
Xue, Y., Pu, L., Yang, L.: Global stability of a predator–prey system with stage structure of distributeddelay type. Commun. Math. Biol. Neurosci. 2015, Article ID 12 (2015)
Smith, C., Reay, P.: Cannibalism in teleost fish, Rev. Fish Biol. Fish., 1, 41–54 (1991)
Walters, C., Christensen, V., Fulton, B., et al.: Predictions from simple predator–prey theory about impacts of harvesting forage fishes. Ecol. Model. 337, 272–280 (2016)
Petersen, A., Nielsen, K.T., Christensen, C.B., et al.: The advantage of starving: success in cannibalistic encounters among wolf spiders. Behav. Ecol. 21(5), 1112–1117 (2010)
Gao, S.: Optimal harvesting policy and stability in a stage structured single species growth model with cannibalism. J. Biomath. 17(2), 194–200 (2002)
Kang, Y., RodriguezRodriguez, M., Evilsizor, S.: Ecological and evolutionary dynamics of twostage models of social insects with egg cannibalism. J. Math. Anal. Appl. 430(1), 324–353 (2015)
RodriguezRodriguez, M., Kang, Y.: Colony and evolutionary dynamics of a twostage model with brood cannibalism and division of labor in social insects. Nat. Resour. Model. 29(4), 633–662 (2016)
Zhang, L., Zhang, C.: Rich dynamic of a stagestructured prey–predator model with cannibalism and periodic attacking rate. Commun. Nonlinear Sci. Numer. Simul. 15(12), 4029–4040 (2010)
Zhang, F., Chen, Y., Li, J.: Dynamical analysis of a stagestructured predator–prey model with cannibalism. Math. Biosci. 307, 33–41 (2019)
Basheer, A., Quansah, E., Bhowmick, S., et al.: Prey cannibalism alters the dynamics of Holling–Tannertype predator–prey models. Nonlinear Dyn. 85(4), 2549–2567 (2016)
Basheer, A., Parshad, R.D., Quansah, E., et al.: Exploring the dynamics of a Holling–Tanner model with cannibalism in both predator and prey population. Int. J. Biomath. 11(01), 1850010 (2018)
Zhang, Z., Ding, T., Huang, W., Dong, Z.: Qualitative Theory of Differential Equation. Science Press, Beijing (1992)
Chen, L., Chen, F.: Dynamic behaviors of the periodic predator–prey system with distributed time delays and impulsive effect. Nonlinear Anal., Real World Appl. 12(4), 2467–2473 (2011)
Chen, L.: Permanence for a delayed predator–prey model of prey dispersal in twopatch environments. J. Appl. Math. Comput. 34(1–2), 207–232 (2010)
Lei, C.: Dynamic behaviors of a stage structure amensalism system with a cover for the first species. Adv. Differ. Equ. 2018(1), 272 (2018)
Lei, C.: Dynamic behaviors of a stagestructured commensalism system. Adv. Differ. Equ. 2018(1), 301 (2018)
Wu, R., Li, L.: Permanence and global attractivity of discrete predator–prey system with Hassell–Varley type functional response. Discrete Dyn. Nat. Soc. 2009, Article ID 323065 (2009)
Wu, R., Li, L.: Permanence and global attractivity of the discrete predator–prey system with Hassell–Varley–Holling III type functional response. Discrete Dyn. Nat. Soc. 2013, Article ID 393729 (2013)
Chen, B.: Dynamic behaviors of a nonselective harvesting Lotka–Volterra amensalism model incorporating partial closure for the populations. Adv. Differ. Equ. 2018(1), 111 (2018)
Chen, B.: The influence of commensalism on a Lotka–Volterra commensal symbiosis model with Michaelis–Menten type harvesting. Adv. Differ. Equ. 2019(1), 43 (2019)
Acknowledgements
The author would like to thank Dr. Liqiong Pu for bringing our attention to the paper of Jiming Zhang.
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The research was supported by the National Natural Science Foundation of China under Grant (11601085).
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Deng, H., Chen, F., Zhu, Z. et al. Dynamic behaviors of Lotka–Volterra predator–prey model incorporating predator cannibalism. Adv Differ Equ 2019, 359 (2019). https://doi.org/10.1186/s1366201922898
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DOI: https://doi.org/10.1186/s1366201922898