Global Stability of a Three-Species System with Attractive Prey-Taxis ()
1. Introduction
In the past few decades, predator-prey systems involving the prey-taxis have attracted more and more scholars to investigate them. Chen et al. [1] reported stationary patterns of a predator-prey model with prey-taxis and investigated the stability of the nonconstant steady states by employing the Crandall-Rabinowitz bifurcation theory. Tu et al. [2] considered the asymptotic behaviors of a parabolic-elliptic chemotaxis system with competitive kinetics and loop of a predator-prey model. Bell and Haskell [3] established the global existence of positive classical solutions and the existence of nontrivial steady states via the bifurcation theory of a predator-prey system. The global existence and uniform boundedness of solutions to a predator-prey system with prey-taxis for general functional responses in any spatial dimensions have been investigated by Ahn and Yoon [4]. The existence of the unique global bounded classical solution is proven, and the steady-state bifurcation, the Hopf bifurcation, and Hopf/steady-state mode interaction are studied via the Lyapunov-Schmidt procedure by Qiu et al. [5]. We recommend more existing results about the predator-prey systems with directed prey-taxis, see Refs. [6] [7] [8] [9] [10], etc.
In this present paper, we focus on a predator-prey model with two predators and one prey as well as the prey-taxis as follows.
(1)
where
and
are predator and prey densities at position x and time t, respectively.
is a bounded domain with its smooth boundary
; constant d describes the diffusive rate of prey; For
,
are the ratios of biomass conversion of predators species;
represent the rates of toxic substances produced by per unit biomass about predators due to prey species are toxic corresponding to the predators;
are the natural mortality of the predators u and v;
describe the half-saturation constant of the predators; s describes the measure of mutual interference among the predator u; two constants r and K in the third equation are the intrinsic growth rate and the maximum environmental capacity of prey species, respectively.
Moreover,
and
are prey-taxis terms. They imply the tendency of predators moving toward the positive direction of the increasing gradient of prey population as
and
. If
and
, we say that predators move toward the opposite direction of the increasing gradient of prey population to avoid group defense by a large number of prey species or volume-filling effect in predator species [11]. Consequently,
and
corresponding to attractive and repulsive prey-taxis, respectively. Moreover,
and
represent the distribution variations of the directed species dispersals [12]. Obviously, they depend on the density of the prey population. All parameters exhibited in the system (1) are set to be positive.
For system (1), define
and
as well as some assumptions
(H1)
(H2)
(H3)
As a result, we can conclude the classifications of the equilibria of system (1). 1) system (1) has a trivial equilibrium
and a semi-trivial equilibrium
; 2) if (H1) holds, system (1) has a boundary equilibrium
, where
3) if (H2) is valid, system (1) has a boundary equilibrium
, where
4) if (H3) is satisfied, system (1) has a unique positive equilibrium
, where
and
with
.
In this present paper, we will establish the global asymptotic stabilities of semi-trivial equilibrium
, boundary equilibria
and the unique positive equilibrium
by constructing some suitable time evolution Lyapunov functions, respectively.
This paper is structured as follows. In Section 2, we perform the main results of the present paper. In Section 3, the local-in-time existence of the classical solution of the model is given. In Section 4, the proofs of the main results are displayed. Finally, some conclusions are made in Section 5.
2. Main Results
Theorem 2.1 Let
be a bounded domain with the smooth boundary
. Suppose
is a classical solution of system (1) with the initial conditions
and
for
. We have the following global asymptotic stability results.
1) For any
and
(2)
then
is globally asymptotically stable.
2) If the condition (H1) holds and
(3)
then boundary equilibrium
is globally asymptotically stable for any
.
3) If the condition (H2)is valid and
(4)
then
is globally asymptotically stable for any
.
4) If the condition (H3) holds and
(5)
as well as
(6)
then
is globally asymptotically stable, where
.
Remark 2.1 From Theorem 2.1, we can find that the global asymptotic stability of the semi-trivial equilibrium
does not involve the prey-taxis coefficients
and
. The global asymptotic stabilities of the boundary equilibria
and
only depend on prey-taxis coefficient
and
, respectively. However, the global asymptotic stability of the unique positive equilibrium
depends on prey-taxis coefficients
and
.
Remark 2.2 The control conditions (3), (4) and (6) of the global asymptotic stabilities of the equilibria only involve the initial spatial density
of prey species but are independent of the initial spatial densities
and
of the predators.
The following conclusion is helpful to obtain the desired results.
3. Existence
Lemma 1 Suppose that
with the smooth boundary
. For any initial conditions
satisfies
for
. Then there is a maximal existence time
such that system (1) has a unique local non-negative classical solution
. Moreover, we have
for
,
, where
.
Proof. Denote by
. Then system (1) takes the form
where
Obviously,
is an upper-triangular matrix and is positive definite since
is valid. Therefore, the local existence can be checked by Amman’s fixed point argument [13]. Now rewrite the first equation of system (1) as follows.
(7)
where
. Obviously, 0 is a lower solution of (7). Therefore, the maximum principle shows
for all
. Combine
with the strong maximum principle,
is valid. By the same way, we have
for all
. Finally, the maximum principle ensures that
for
. This ends the proof.
In the sequel, we shall give proof of Theorem 2.1 by constructing some suitable time evolution Lyapunov functions.
4. Proof of Theorem 2.1
1) For
, define the following Lyapunov function
(8)
Then we deduce
Consequently,
and
is globally asymptotically stable if (2) holds.
2) Define
(9)
As a result, one deduces
where
and
By using
one yields
due to (3) is valid. For
, we have
where we define
in
, and the matrix
is
Accordingly, we have
and
as (3) holds. These
imply
and
is globally asymptotically stable.
3) Consider the following function
(10)
Straightforward computation showing
where
and
Note that
we get
if (4) is satisfied. For
, we have
where denote by
in
and
It is clear that
and
since
. Consequently,
and thus
is globally asymptotically stable.
4) Introducing the following time evolution Lyapunov function
(11)
Direct computations illustrate that
where
and
By employing these facts
we can obtain
here we use the Condition (5). Moreover
where the vector function
is given by
in
and
We can obtain
as well as
if
Thence
is a nonnegative definite matrix, which gives
. We conclude that
is globally asymptotically stable. These end the proof.
5. Conclusions
This present paper deals with the global asymptotic stability of a three-species predator-prey model with prey-taxis. This system possesses a semi-trivial equilibrium
, two boundary equilibria
and
, and a unique positive equilibrium
. By constructing some suitable Lyapunov functions, we establish their global asymptotic stability, respectively. It is concluded that the prey-taxis coefficients
can not influence the global asymptotic stability of the semi-trivial equilibrium
. Also, the global asymptotic stability of two boundary equilibria
and
rely on the single prey-taxis coefficient
and
, respectively. However, the global asymptotic stability of the unique positive equilibrium
is determined by prey-taxis coefficients
and
. These phenomena suggest that the prey-taxis has an influence on the global asymptotic stability of the equilibria of the System (1). Consequently, we will continuously explore the complicated dynamics of the System (1) with prey-taxis effect in the future.
Acknowledgements
This work was supported by the National Natural Science Foundation of China (No. 12002297) and the China Postdoctoral Science Foundation (No. 2021M701118).