Abstract
In this paper, we consider a predator-prey diffusion model incorporating hunting cooperation and predator-taxis. Firstly, we establish the global existence of a classical solution for the model in any spatial dimension. Secondly, we analyze the stability/instability caused by predator-taxis, and we observe that predator-taxis play a key role in inducing stability changes. Specifically, if the positive equilibrium is stable for the corresponding reaction-diffusion model, the attractive predator-taxis can further stabilize the system, while the repulsive predator-taxis may lead to a change in spatial stability, if the positive equilibrium is unstable for the corresponding reaction-diffusion model, the attractive predator-taxis makes the model remain unstable, while the repulsive predator-taxis has a stabilizing effect. Finally, numerical simulations are employed to validate the obtained results.
MSC:
35A09; 35K59
1. Introduction
The predator-prey relationship is a common phenomenon in nature and has garnered significant attention in the field of biomathematics research. Through conducting a investigation into the predator-prey model, we can reveal the evolution law of populations.
Hunting cooperation is a prevalent form of species interaction, which refers to the cooperative behavior exhibited by certain predators in the process of capturing prey. Hunting cooperation plays an important role in maintaining ecological diversity and regulating population density. Hunting cooperation can occur between individuals of the same species, such as lions, wild chimpanzees, fish, ants, birds, and so on [1,2,3,4,5]. Additionally, hunting cooperation behavior may also exist between different species, such as cheetahs and jackals preying on deer or badgers and coyotes targeting ground squirrels [6].
To reveal the impact of hunting cooperation by predators on species extinction, Duarte et al. [7] investigated a tri-trophic food chain model incorporative cooperative hunting, and they found that predators were more sensitive to extinction when hunting cooperation increased. Berec [8] considered hunting cooperation in the predator-prey model where the Holling II functional response is employed. Berec found that hunting cooperation exerts a destabilizing influence on predator-prey dynamics. Alves and Hilker [9] proposed that the attack rate of a predator species would increase with the increase in predator density due to foraging promotion. Therefore, they established a series of predator-prey models with hunting cooperation and Holling type functional responses, and concluded that cooperative hunting can improve the persistence of predator populations. Fu and Zhang [10] studied a Holling II type predator-prey diffusion model incorporative hunting cooperation
where u, v denote prey and predator population densities, respectively. and are the per capita birth rate and carrying capacity for prey species, h designates the average hunting time of a predator for prey, represents the rate of predator cooperation in hunting. Fu and Zhang [10] investigated linear stability and Turing instability of positive constant steady states, and analyzed the existence and stability for the Hopf bifurcated periodic solutions of this model.
In predator-prey models, the phenomenon of predators moving towards areas with higher prey density, known as prey-taxis, has been extensively studied. In 1987, Kareiva and Odell [11] first proposed an ecological model with prey-taxis to elucidate the directional movement of species. In the following decades, scholars have established numerous models with prey-taxis to investigate the dynamic relationship between predators and prey [12,13,14]. Recently, a novel form of predator-taxis has been developed and distinguished from prey-taxis, in which prey escapes from areas with a high predator density to avoid being captured. This means that the prey is moving in the direction of the predator. Several researchers have also explored and constructed several ecological models involving predator-taxis, see [15,16,17]. These models assumed that prey would move toward a lower density of predators to avoid dangerous situations.
Hunting cooperation and predator-taxis are prevalent in real ecosystems, so to better describe biological phenomena, we discuss the following predator-prey diffusion model that incorporates hunting cooperation and predator-taxis
where is a bounded domain in , represents the outward unit normal vector to , the homogeneous zero-flux condition ensures that (2) is self-contained for . Additionally, the initial data , are smooth non-negative functions that are not identically zero. The term denotes the directional movement of prey, and represent the sensitivity coefficient of predator-taxis. In particular, when , the prey will move in the direction of the gradient of predators because of group defense when sensing the risk of predation, and then the predator–taxi is attracted; when , it means that the prey exhibits an opposite movement direction for the gradient of predator, aiming to evade predation, and the predator-taxi is called repulsive. The model (2) well describes the effects of predator-taxis and hunting cooperation on a predator-prey diffusion model. From the perspective of mathematical research, by studying the dynamic behavior of the model (2), we can understand the relationship between species in the ecosystem more clearly so as to provide some theoretical support for maintaining a balance of the ecosystem and preventing species extinction.
The organization of this paper is as follows. Section 2 presents the global existence of a classical solution to model (2). In Section 3, we analyze the instability caused by predator-taxis for positive equilibrium in the model (2). Section 4 uses numerical simulations to verify the theoretical results. Finally, concise conclusions are provided in Section 5.
2. Global Existence of Classical Solution
In this section, we prove the global existence of a solution for the model (2) in any spatial dimensions. Moreover, throughout this section, we denote by generic positive constants that may differ from line to line. For simplicity, write instead of .
2.1. Local Existence and Preliminary
We firstly employ the abstract theorem of the quasilinear parabolic system [18,19] to establish the local existence of a solution for model (2).
Lemma 1.
Assume the initial data with and . Then, we have the following:
- (i)
- There exists a positive constant such that model (2) admits a unique local-in-time classical solution , which satisfies;
- (ii)
- There exists a constant such that;
- (iii)
- There exists a constant such that;
- (iv)
- If , we have.
Proof.
The local existence and uniqueness of the solution to (2) follows from Theorem 7.3 and Corollary 9.3 in [18] or Theorem 14.4 and 14.6 in [19], and the extensibility criterion (5) can be obtained directly from Theorem 15.5 in [19]. By utilizing the strong maximum principle on model (2), it can be find that and in .
To prove (ii), we integrate the first two equations of (2) over , which implies that
By employing the Gronwall inequality, one obtains (3).
Next, we establish the upper bound of , by the second equation in (2) and , we have
Hence, we easily obtain that there exists a constant such that from Theorem 3.1 in [20] and the comparison principle. □
To establish the global-in-time of the solution, we next recall some preliminary estimates. For , we represent the sectorial operator by A and define it as
similarly, we denote where and possess the same properties as A with a scaling. Here, we will give some properties for A, but applying the properties of and in the subsequent discussion.
Lemma 2
([21]). Let , , and . Then, for any , there exists such that
where and satisfies
If, in addition , then for any , there exist and such that
with the associated heat semigroup is known to map into . Additionally, for all and , there exist and such that
is valid for any –valued .
Lemma 3
(Gagliardo-Nirenberg interpolation inequality [22]). Suppose , and , where for , and for . Then, for given by: and some , we have
for any .
2.2. Global Existence of Solution
In this section, we study the solution to model (2) and its global existence. To begin with, we provide a bound for .
Lemma 4.
Assume to be a classical solution of (2). Then there exists a constant such that
Proof.
Let be chosen, satisfying , fix and . Rewrite the equation of v in (2) as follows
in view of the variation-of-constants formula, one yields
From (9) and (10), we find that for any ,
where is a Gamma function, then due to . Therefore, we can obtain
□
Next, we state is uniformly bounded in for any
Lemma 5.
Assume to be a classical solution of (2). Then for any , there exists a constant such that
Proof.
For , the equation of u in (2) is multiplied by and then integrated over , one has
this implies
From (12), we have
where and . Fix with
Combining (14)–(16), we find that
Therefore, we have
□
Now we prove that is uniformly bounded for any .
Lemma 6.
Assume to be a classical solution for (2). Then there exists a constant such that
Proof.
The equation of u in (2) is written as
The use of the variation-of-constants formula in (17) to obtain
Then, we discuss the -bounded of and , respectively.
From the parabolic maximum principle, we have
where , , , .
In Lemma 2, letting , and , taking , we can establish that . Consequently, there exists and such that
from Lemmas 4 and 5, we can obtain that
Then
where and , then we find that is positive.
Assume that , where is the maximum existence time. From Lemmas 4 and 6 with some , we have
this is contrary to Lemma 1 (iv), it can be inferred that and, consequently, the solution remains bounded for all . On the basis of Lemmas 1, 4 and 6, we have the following conclusion.
Theorem 7.
Let the initial data with and . Then, model (2) admits a unique global-in-time classical solution satisfying
where is a positive constant that depends on the initial value, but not on t.
3. Stability/Instability Caused by Predator-Taxis
In this section, the instability of the positive constant steady state for model (2) caused by predator-taxis behaviour is investigated. For convenience, we consider the case of (2) in one-dimensional space and assume , then model (2) can be rewritten as
We denote the positive equilibrium of (23) by , and it can be easily to show that , while corresponds the positive root of the following equation
where .
First, let us assume
Observing the facts and , if is true, then can be obtained, where the sign of the coefficients of is or . In both cases, the symbol changed only once. According to Descartes’ rule of signs [23], has a unique positive root, which means that model (23) exhibits a unique positive equilibrium when condition holds true. To simplify matters, we will assume condition to hold throughout the remainder of the discussion.
By simple calculation, we know that . The characteristic equation of (23) is
where
and be the eigenvalues of on subject to the zero-flow boundary condition.
According to the standard linear stability theory, for any non-negative integer k, the positive equilibrium is locally asymptotically stable if and only if all the roots of the characteristic equation have negative real parts, is unstable if the characteristic equation has at least one root with a positive real part for some non-negative integer k.
Since we are interested in the predator-taxis-driven instability, we take the assumption
It can be easily shown that the condition guarantees is locally asymptotically stable in the corresponding ordinary differential equation model ().
Let
Then, we can deduce the following theorem.
Theorem 8.
Suppose and hold. For model (23), then we have
- (i)
- If , then for all , is always locally asymptotically stable;
- (ii)
- If and , then is locally asymptotically stable when and it is unstable when ;
- (iii)
- If , then is locally asymptotically stable when and it is unstable when or .
Proof.
A simple calculation gives that for and for with
Then, there exists such that when , we have . □
From the assumption , we know that for all , thus, we only discuss the sign of .
- (i)
- If and , it is evident that for any , then exhibits locally asymptotically stability;
- (ii)
- If , together with , one has for any . When , then for any , thus is locally asymptotically stability. When , we have for some , which implies is unstable;
- (iii)
- If , then is unstable for the corresponding reaction–diffusion model. From , it follows that for any . When , we observe that for any , and then is locally asymptotically stability. When and , we have for some , then is unstable.
- Next, we show that can reach its maximum on . Set
Remark 9.
Theorems 8 (i) and (ii) show that when the positive equilibrium is stable with respect to the reaction-diffusion model, the attractive predator-taxis can further stabilize the system, while the repulsive predator-taxis may lead to a change in spatial stability, which means the formation of the pattern caused by the predator-taxis. Theorem 8 (iii) shows that when the positive equilibrium is unstable with respect to the reaction-diffusion model, the attractive predator-taxis make the model remain unstable, while the repulsive predator-taxis have a stabilizing effect.
Remark 10.
From an ecological point of view, a stable equilibrium means that over time, predator and prey species will eventually converge at this point, and their numbers will remain constant, thus achieving permanent coexistence. The conclusion of Theorem 8 shows that attractive predator-taxis are beneficial to species coexistence.
4. Numerical Simulations
In this part, we give some numerical simulations in order to verify the above theoretical analysis by utilizing the MATLAB software. We fixed , , , and set parameter
It is evident that model (23) possesses a trivial equilibrium , a boundary equilibrium , and a unique positive equilibrium . Note that under the given parameters (26), both conditions and are satisfied, rendering stable with respect to the corresponding ODE model (i.e., ). When we choose , the equilibrium is unstable with respect to the corresponding reaction-diffusion model (see Figure 1), by performing calculations , taking , is unstable with respect to model (23), which shows that positive predator-taxis have stabilizing effects (see Figure 2). When we choose , is locally asymptotically stable with respect to the corresponding reaction-diffusion model (see Figure 3), the calculation gives that , taking , is stable with respect to the model (23), indicating that the negative predator-taxis have a destabilizing effect (see Figure 4).
5. Concluding Remarks
This paper mainly discusses the dynamics of the predator-prey diffusion model with hunting cooperation and predator-taxis, where hunting cooperation refers to the cooperative behavior of some predator populations in the process of capturing prey. The predator-taxis effect refers to the response of prey to different predator distributions, i.e., the prey may move in the direction of a low predator gradient to avoid being captured by predators, or it may move in the direction of a high density of prey to defend against predator attacks. Hunting cooperation and predator-taxis have far-reaching implications for protecting endangered species and maintaining sustainable ecosystems.
Firstly, the global existence and uniform boundedness of a classical solution of the model are proven strictly. Secondly, the local stability of a positive equilibrium is discussed through linearization analysis. Finally, we use numerical simulations to visualize the results. In addition, it can be seen from [10] that the stability of the reaction-diffusion model depends on the ratio of diffusion coefficients. Combined with the discussion results of this paper, we found that in the same region, if this ratio is less than a critical value, it means that the predator occupies an advantageous position, which indicates that due to strong predation pressure, the prey should stay away from the predator’s habitat to avoid being predation. On the contrary, if this ratio is greater than a critical value, the situation is more favorable for the prey, which means that in the face of an attack by predators, the prey must collectively gather together and resist to obtain more survival opportunities, which is more conducive to the long-term development of the population.
Funding
This work is supported by the National Natural Science Foundation of China (No. 12161080).
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Data are contained within the article.
Acknowledgments
The author would like to thank the referees for providing very helpful comments and suggestions.
Conflicts of Interest
The author declares no conflicts of interest.
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