Bifurcation and Turing Pattern Formation in a Diffusion Modified Leslie-Gower Predator-Prey Model with Crowley-Martin Functional Response ()
1. Introduction
The interaction between predators and prey is an important process in maintaining ecological balance in ecosystems. To better understand the dynamic behavior of this interaction, researchers have proposed many mathematical models to describe the evolution of predator-prey systems. In recent years, the evolution of the population system has an important reference significance for the protection of the ecosystem and has obtained [1]-[17] many valuable results. The Leslie-Gower model is a classic predator-prey model that can describe how the populations of predators and prey change over time [3] [4]. However, this model assumes that the mortality rate of the prey population is independent of density, which may not be consistent with reality in some cases. To address this issue, researchers have introduced diffusion terms to modify the Leslie-Gower model, allowing it to better describe the death process of the prey population [18]-[23]. The Crowley-Martin function is a commonly used form to describe the response strength of predators to changes in prey density. This function has been widely applied in predator-prey models.
The growth function of the traditional logistic model is
, where r represents the internal growth rate of the prey without the action of the predator. It is noted that the logistic equation
and the average growth rate
is a linear function of the prey. However, under the action of
environmental poisons, this assumption is unrealistic for food limited populations. In the early 1960s, Smith [7] conducted experiments on large dapsophila populations in the laboratory, and the results showed that the hypothesis of linear growth rate was inconsistent with large dapsophila populations, and demonstrated that population growth needed food to sustain, but only needed food to maintain when the population reached saturation. Therefore, Smith modified the Logistic model and formed the “limited food” model, sometimes called the “limited resources” model [8] [9] [10] [11] [24]. The model is given as follows
where, a represents the resource limitation parameter of the population and
represents the mass replacement rate of the population at k. This is a further development of the Logistic model. Adding the thinking of the above questions, Yue et al. [8] discussed the properties of the model solution by studying the diffusion Holling-Tanner predator-prey model with Smith growth, and obtained the existence of non-constant of the steady-state system. Jiang et al. [11] mainly studied the diffusion delay model with Smith growth and group behavior, analyzed the existence and stability of Hopf bifurcation in this model, and verified the theoretical results by numerical simulation. Han et al. [24] discussed the dynamic behavior of a space and time discrete predator-prey system with Smith growth function. By the stability analysis, the parametric conditions are gained to ensure the stability of the homogeneous steady state of the system. Xiaozhou Feng et al. [25] proposed a modified Leslie-Gower predator-prey ODE model with Smith growth rate and B-D functional response term, and the systematic study was conducted on the dynamic behavior of the model. Combining the advantages of the above models, the following models are proposed by us:
(1)
where u and v are prey and predator densities and r1 and r2 denote their intrinsic growth rates, respectively; a represents the resource limitation parameter of the population, M is the rate at which the predator consumes the prey, B and C are normal numbers, D and E represent the conversion rate of prey into predators biomass and the carrying capacity of the population respectively,
are positive constants, and a is a non-negative constant, if
, we retain a classical Holling type II Lotka-Volterra model with logistic growth of the prey.
For simplicity, we introduce the dimensionless variables as in [2],
the dimensionless parameters
system (1) can be simplified as follows:
(2)
In real world, the spatial distributions of the predator and prey are inhomogeneous within a fixed bounded domain, and each species has a nature tendency to diffuse to areas of smaller population concentration [26]. Hence, we should use reaction-diffusion equations to describe spatial dispersal of each species, so the system (2) is further modified into
(3)
where
is the outer unit normal vectors of the boundary. The homogeneous Neumann boundary condition shows that the predator-prey system is self-contained and the population flow on the boundary is zero. The positive constants d1 and d2 are diffusion coefficients, and the initial values are nonnegative continuous functions.
The rest of this paper is organized as follows. In Section 2, we analyze the local asymptotic stability, and discuss various common bifurcation problems. In Section 3, we firstly consider the Turing instability of the coexistence equilibrium for reaction-diffusion system (3). Then we discuss the global asymptotic stability of the coexistence equilibrium for reaction-diffusion system (3).
2. Stability and Bifurcations of the ODE Model
2.1. Equilibria and Their Stability
Let
(4)
All the equilibrium solutions of the system are as follows
(1)
, which indicates both prey and predator are extinct.
(2)
, which indicates the predator is extinct.
(3)
, which indicates the prey is extinct.
(4)
, which indicates the coexistence of prey and predator populations.
Where
is positive equilibrium point of (2), then
,
here is satisfied the following cubic equations
(5)
where
Similar to the references [27] [28] we obtain:
Case 1: When
, system (2) has a positive equilibrium
.
Case 2: When
,
(i)
(
and
), system (2) has a triple real root:
(ii)
, system (2) has a non-degenerate single real root
and a degenerate double real root
.
Case 3: When
, system (2) has three unequal positive real roots
,
,
.
Next, the stability of the system is studied on this equilibrium solution.
By calculating the eigenvalues of Jacobin matrix J on (2) as follows
We can establish the following conclusions.
(1) The eigenvalues of Jacobin matrix J at
are 1 and
, so equilibrium solution
is a saddle point, and it is unstable.
(2) The eigenvalues of Jacobin matrix J at
points the eigenmultinomial matrix is
The characteristic polynomial corresponding to this matrix is
Since
, so that
is a saddle point, and the equilibrium point
is unstable.
(3) The eigenvalues of Jacobin matrix at point
points the eigenmultinomial matrix is
The characteristic polynomial corresponding to this matrix is
If
, there
,
, therefore, the equilibrium point
is asymptotically stable.
If
, there
, it follows that
is a saddle point, so the equilibrium point
is unstable.
(4) We mainly discuss the stability of the positive equilibrium point
. By calculation and bifurcation theory, we establish the following theorem.
In the following, we analyze the stability of the positive equilibria of model (2). Let
be a positive equilibrium of model (2). Then the Jacobin matrix of model (2) at
is
(6)
where
(7)
The characteristic polynomical is
(8)
where
and
Thus, we have the following conclusions [29].
Theorem 2.1. Assume that
.
Define
(i) If
and
(H1)
,
then the positive equilibrium
is locally asymptotically stable.
(ii) If (H1) and
(H2)
,
are satisfied, then the positive equilibrium
is unstable when
.
(iii) If
(H3)
,
then the positive equilibrium
is a saddle point.
Remark 2.2. If the case (i) of Theorem 2.1 holds,
is permitted to be positive or negative. If
, that is,
(9)
then we have
which indicates that (H1) holds.
must be positive when case (ii) in Theorem 2.1 holds. Moreover, we can see that conditions (H1) and (H2) can hold simultaneously. Furthermore, from (9) (H1) and (H3), we know that
is positive in Theorem 2.1 case (iii).
2.2. Hopf Bifurcation
In the following, we analyze the existence of Hopf bifurcation at the interior equilibrium
(
) by choosing c as the bifurcation parameter [30] [31]. In fact, s can be regarded as the intrinsic growth rate of predators and plays an important role in determining the stability of the interior equilibrium and the existence of Hopf bifurcation. Denote
From the above discussions, if
, then
, which together with
yield that
has a pair of purely imaginary eigenvalues
.
We claim that the transeversal condition is satisfied. In fact, if
are the roots of
, then
,
. Hence,
This shows that the transversality condition holds. Thus (2) undergoes a Hopf bifurcation about
as c passes through the
.
To understand the detailed behaviour of model (2) around
, we need a further analysis of the normal form. We translate the interior equilibrium
to the origin by the transformation
,
. For the sake of convenience, we still denote
and
by u and v, respectively. Thus, the local system (2) is transformed into
(10)
Expanding model (10) in power series around the origin produces the following model
(11)
where
(12)
and
Set the matrix
where
It is easy to obtain that
When
, we have
(13)
By the transformation
, model (11) can be rewritten as
(14)
where
Rewrite (14) in the following polar coordinates form
(15)
then the Taylor expansion of (15) at
yields
(16)
In order to determine the stability of the Hopf bifurcation periodic solution, we need to calculate the sign of the coefficient
, which is given by
(17)
where all the partial derivatives are evaluated at the bifurcation point
, and
Thus, we can determine the value and sign of
in (17).
Recall that
from the Poincaré-Andronov-Hopf Bifurcation theorem, we can summarize our results as following.
Theorem 2.3. Assume
hold. Then system (2) undergoes a Hopf bifurcation at the interior equilibrium
when
. Furthermore,
(i)
determines the stabilities of the bifurcated periodic solutions: if
(>0); then the bifurcating periodic solutions are stable(unstable);
(ii)
determines the directions of Hopf bifurcation: if
(<0) then the Hopf bifurcation is supercritical (subcritical).
2.3. Transcritical Bifurcation Analysis
Theorem 2.4. The prey-free equilibrium
will experience a transcritical bifurcation around
.
Proof. If
is chosen as the bifurcation parameter, then system (2) has a zero eigenvalue and a negative eigenvalue
, the Jacobian matrix becomes
In this case, the eigenvectors of matrices
and
are respectively:
Let
, then through calculation we get
and further there is
, it means that system (2) doesn’t have a saddle-node bifurcation near
. Also
Hence, system (2) will produce a transcritical bifurcation at
through the Sotomayor’s Theorem.
2.4. Numerical Simulations
In this subsection, we provide numerical simulations to support the analytical results obtained above. The ODE model (2) have seven parameters: a, b, c, d, e, s, m. We illustrate these results by fixing parameters a, b, d, e, s and m and taking the magnitude of interference among predators c as the control parameter.
Example 2.5. We choose parameters as follows
(18)
Figure 1 shows the phase portraits of model (2) with parameters in (18). In this case, the model (2) has four equilibria: Two saddle points
,
, a nodal source point
, a unique coexistence point
. By simple computation, we can obtain that
. In Figure 1(a),
,
is an unstable spiral source and the model exhibits a limit cycle. In Figure 1(b),
,
is a local asymptotically stable spiral sink. Moreover, when c passes through
from the left-hand side of
,
will lose its stability and Hopf bifurcation occurs, that is, a family of periodic solutions bifurcate from the positive equilibrium. Since
, it follows from Theorem 2.3 that the Hopf
Figure 1. Phase portraits of model (2) with parameters in (18). (a)
; (b)
.
bifurcation is supercritical and the bifurcation periodic solutions are orbitally asymptotically stable.
3. Turing Instability and Bifurcation of the Reaction-Diffusion Model (19)
In this section, we investigate the reaction-diffusion model (3) to derive the Turing unstable parameter region of the positive equilibria, and the existences, direction and stability of the Hopf bifurcation periodic solutions which describes the spatiotemporal pattern formation.
3.1. Turing Instability of the Positive Equilibria
It is well-known that the equilibrium
is Turing unstable if it is stable equilibrium of the ODE model (1) but is unstable for the PDE model (3) [32] [33] [34] [35].
For simplicity, we take the spatial domain Ω as the one-dimensional interval
, and study the following model
(19)
Notice that the operator
with no-flux boundary conditions has the following eigenvalues and corresponding eigenfunctions
The linearized system of (19) at
is
(20)
where
is the Jacobian matrix defined in (6) and
. M is a linear operator with domain
where
is a real-valued Sobolev space.
According to the standard linear operator theory, if all eigenvalues of the operator have negative real parts, then
is asymptotically stable. If some eigenvalues have positive real parts, then
is unstable. Define
It is clear that the eigenvalues of the operator M are given by the eigenvalues of the matrix
. The characteristic equation of
is
(21)
where
By analyzing the root distribution of the characteristic Equation (21), we can draw the following theorem.
Theorem 3.1. Suppose that
holds, the equilibrium point
of the system (2) is asymptotically stable when
, and the equilibrium point
is locally asymptotically stable in the system (24) if and only if the following assumptions are satisfied
(H1)
,
(H2)
and
,
whereas
is unstable with respect to the PDE model (19), that is, Turing instability occurs if
(H3)
Proof. First, it is clear that,
for
from the definition of
, and
. So
for all
. Therefore, the signs of real parts of roots of (21) are determined by the signs of
, respectively. For the sake of convenience, define
which is a quadratic polynomial with respect to
. The symmetric axis of graph
is
. When
,
for all
since
. When
,
will take the minimum value at
, and
The hypothesis (H1) implies that
, (H2) implies that
and
. In both cases,
for all
. So all the roots of (21) will have negative real parts,
is asymptotically stable.
When (H3) holds,
and
, (21) has at least one root with positive real part, therefore
is unstable. This indicates that the Turing instability occurs.
Theorem 3.2. Assume that
and (9) hold. Then the unique positive
in (19) is locally asymptotically stable.
Proof. Let
,
,
. Then the linearized system of (19) at
is
(22)
and the eigenvalues of the operator M are the eigenvalues of the matrix
,
.
The characteristic equation of
is
where
and
are defined as in Section 2.
If (9) holds, then
and
. The roots
,
of
all have negative real parts.
We claim that there exists a positive constant
such that
(23)
Let
, then
and
So, the two roots
of
always have negative real parts. Let
then
. By continuity, there exists
such that the two roots
of
satisfy
,
. As a result,
, for
. Let
and
. Thus, we obtain the inequation (23), which completes the proof.
3.2. Hopf Bifurcation Analysis
In this subsection, we seek for the possible Hopf bifurcation points and explore the direction and stability of the bifurcation periodic solutions of model (19) with spatial domain
. We only discuss the Hopf bifurcation around
. The Hopf bifurcation around
and
can be similarly considered [36].
We take the transformation
,
, and still denote
by
. Then model (19) can be rewritten as
(24)
Let
be the conjugate operator of L defined by (20). Then
(25)
where
with the domain
. Let
It is easy to verify that
for any
,
, and
,
,
,
, where denotes the inner product in
. Similar to [29], let us decompose
with
and
.
For any
, there exist
and
such that
Thus,
The model (19) in
coordinates becomes
(26)
with
, where f and g are defined as (11). Some direct calculations give
By Appendix A of [35], model (26) possesses a center manifold, one can write
in the form
Thus,
This implies that
, so that
, the equation becomes,
where
where
and
with
It can conclude from the above calculation
then
(27)
which together with
determine the stability and direction of the bifurcated periodic solutions.
Theorem 3.3. Assume
hold. Then model (19) undergoes a Hopf bifurcation at
.
(i) If
, then the Hopf bifurcation is supercritical and the bifurcating periodic solutions are asymptotically stable on the centre manifold. Furthermore, they are orbitally asymptotically stable for model (19) if (H1) or (H2) holds, and unstable if (H3) holds.
(ii) If
, then the Hopf bifurcation is subcritical and the bifurcating periodic solutions are unstable.
3.3. Numerical Simulations
In this subsection, we give some numerical simulations to illustrate our theoretical analysis, we consider model (19) in one-dimensional space.
Example 3.4. We choose parameters as follows
(28)
Then
, and the unique positive equilibrium
in model (2) is locally asymptotically stable. If we choose
, then (H2) holds, by Theorem 3.1, the equilibrium
in model (19) is still locally asymptotically stable (see Figure 2). If we choose
, then (H3) holds, by Theorem 3.1, the equilibrium
in model (19) becomes unstable, this means that the Turing instability of the equilibrium solution happens (see Figure 3).
Example 3.5. We choose parameters as follows
(29)
In this case, we have
,
. By Theorem 3.3, the supercritical Hopf bifurcation occurs at
. Notice that
. The unique positive equilibrium
in model (19) is unstable and bifurcating periodic orbits exist. If we choose
, then (H2) holds, the bifurcating periodic orbits are orbitally asymptotically stable (see Figure 4). If we choose
, then (H3) holds, so the bifurcating periodic orbits are
Figure 2. Numerical simulations of the stable equilibrium of model (19) with parameters in (28) and
.
Figure 3. Numerical simulations of the Turing instability of the equilibrium of model (19) with parameters in (28) and
.
Figure 4. Numerical simulations of the stable bifurcating periodic solution of model (19) with parameters in (29) and
.
Figure 5. Numerical simulations of the Turing instability of bifurcating periodic solution of model (19) with parameters in (29) and
.
Turing unstable (see Figure 5).
4. Conclusion and Discussion
The pattern formation of ecosystem has always been an important and fundamental topic in ecology. In this paper, we consider a diffused modified Leslie-Gower predator-prey system with a C-M functional response under homogeneous Neumann boundary conditions. Firstly, the local asymptotic stability and bifurcation in corresponding ODE systems are studied. (i) At the equilibrium point
, Hopf bifurcation occurs when
. (ii) At the equilibrium
point
, transcritical bifurcation occurs when
. Secondly, we consider
the Turing (diffusion-driven) instability of reaction-diffusion systems in co-equilibrium when the spatial domain is a bounded interval, which produces a spatially inhomogeneous pattern. Besides, we investigate the existence and direction of Hopf bifurcations and the stability of periodic solutions of bifurcations in a reaction-diffusion system, which exhibits a time-periodic pattern. Finally, we discuss the interaction of Turing instability and Hopf bifurcation in a reaction-diffusion system that exhibits a spatio-temporal pattern. Our theoretical results further suggest that predator-prey interference and predator feeding strategies are determinants of spatial and spatio-temporal patterns generated through predator-prey interactions in a uniform environment.
Since the C-M functional response function is more general than the B-D functional response function and contains the Holling II functional response function, we would like to point out that our results are still valid for the diffuse Leslie-Gower predator-prey system and the diffuse Holling-tanner predator-prey system with the B-D functional response.