Abstract
This paper investigates the complex dynamics of a ratio-dependent predator–prey model incorporating the Allee effect in prey and predator harvesting. To explore the joint effect of the harvesting effort and diffusion on the dynamics of the system, we perform the following analyses: (a) The stability of non-negative constant steady states; (b) The sufficient conditions for the occurrence of a Hopf bifurcation, Turing bifurcation, and Turing–Hopf bifurcation; (c) The derivation of the normal form near the Turing–Hopf singularity. Moreover, we provide numerical simulations to illustrate the theoretical results. The results demonstrate that the small change in harvesting effort and the ratio of the diffusion coefficients will destabilize the constant steady states and lead to the complex spatiotemporal behaviors, including homogeneous and inhomogeneous periodic solutions and nonconstant steady states. Moreover, the numerical simulations coincide with our theoretical results.
1. Introduction
The predator–prey interaction is a significant topic in the studies of populations, communities, and ecosystems and has attracted much attention from scholars. Since the introduction of the classical Lotka–Volterra model, predator–prey models have been continuously improved and developed, but there are still many ecological problems that need attention and solving [1,2,3,4]. We can use the following form of an ordinary differential equation to represent the predator–prey system
where u and v are the densities of prey and predators, respectively. Here, is the natural growth rate of the prey population in the absence of predators, is the predator growth rate without prey, c is the conversion rate from predation, and is the functional response. Generally, functional responses can be divided into two categories: prey-dependent functional response and predator-dependent functional response. Prey-dependent functional response means that is the function of prey density only; see [4,5,6,7], for example. However, in predator-dependent predator–prey models, the function depends on the densities of both predator and prey. In [8], the authors proposed that a functional response should depend on the ratio of prey-to-predator density, which is supported by several laboratory observations and has been widely used in predator–prey systems. Since then, the ratio-dependent predator–prey models have gained much attention over many decades. Compared with the traditional prey-dependent predator–prey models, the ratio-dependent models can exhibit richer and more reasonable dynamical behaviors [9,10,11,12,13].
In fact, there are still other factors, as well as the functional response, that should be considered in the study of the predator–prey systems. Stephens et al. [14] suggested that the Allee effect, proposed by Allee [15], can be defined as a positive relationship between any component of individual fitness and the number or density of conspecifics. In the 2000s, Kramer et al. [16] suggested that the Allee effect can be caused by mate limitation, predator satiation, cooperative feeding or defense, habitat alternation, dispersal, etc. Their study showed that the Allee effect plays a key role in numerous systems. Later, Merdan [17] studied the effect of the Allee effect on the stability of a Lotka–Voterra model. The study demonstrated that the presence of the Allee effect makes the system take a longer time to reach the stable equilibrium and reduces the densities of both prey and predators at the stable equilibrium. Due to the significant effect on population dynamics, the Allee effect has gained increasing attention; see [18,19,20,21,22,23,24,25,26,27], for example. In view of human needs, the harvesting of biological resources should also be taken into account in predator–prey models. In [28], Xiao et al. considered the ratio-dependent predator–prey model with constant harvesting of predators as follows:
where h represents the harvesting rate; for more background about (1), we refer readers to [28] and the references therein. For system (1), the authors obtained the occurrence of numerous types of bifurcations, including the Bogdanov–Takens bifurcation, the saddle-node bifurcation, and the supercritical and subcritical Hopf bifurcations. From the perspective of biology, it is more reasonable that the harvesting rate function should be proportional to the harvested population. In [29], Chakraborty et al. proposed the modified ratio-dependent predator–prey system with nonconstant predator harvesting as follows:
where is the harvesting rate; for more details concerning system (2), we refer readers to [29] and the references therein. This study revealed that when the harvesting rate is very high or low, the predator will eventually be extinct. In [30], the authors discussed the local stability of system (2). They gave the conditions under which the interior equilibrium is stable or unstable, a focus or a center. Their study showed that the predator harvesting rate plays a key role in the stability of the interior equilibrium of system (2), and the presence of predator harvesting makes system (2) exhibit much richer dynamical behaviors.
As is well known, the predators and prey distribute inhomogeneously in different locations; therefore, diffusion should be taken into account in ecological and biological models. Based on the fact that diffusion may destabilize the steady state and induce the occurrence of Turing instability, many scholars have investigated the diffusive predator–prey systems; see [13,31,32,33,34], for example. Although the ratio-dependent predator–prey system has been extensively investigated, a study concerning the system incorporating the Allee effect, predator harvesting, and diffusion has not been seen yet. Based on this, we consider a diffusive system with the Allee effect in prey and predator harvesting as follows:
where K is the carrying capacity for the prey, is the maximum per capita growth rate of the prey, G is the capturing rate, is the conversion rate, L is the predator death rate, and H is the harvesting rate. Further, is the Allee threshold, and and are the diffusion coefficients. Let
and, by dropping the hats of the notations, we can obtain the corresponding diffusive system with a homogeneous Neumann boundary and initial conditions as follows:
For system (4) without the Allee effect, Gao et al. [34] studied the existence and properties of a Hopf bifurcation, provided the conditions for the occurrence of Turing instability induced by diffusion, and proved the existence and non-existence of the non-constant steady states. When the harvesting term in (4) is absent, i.e., , Rao and Kang [13] investigated the effect of diffusion and the Allee effect on the dynamical complexity of the system. Their results reveal that the strength of the Allee effects plays a key role in the formation of distinct spatial patterns.
In this paper, we aim to explore the joint effect of diffusion and harvesting effort on the dynamics in system (4). Notice the fact that the term has no definition at ; we assume that as in [9,10]. The rest of this article is organized as follows. In Section 2, we first discuss the existence of positive equilibria. Then, we investigate the dynamics of the ODE system corresponding to system (4). In particular, using the harvesting rate as the bifurcation parameter, we study the stability of the positive equilibria, verify the existence of a Hopf bifurcation, and derive the explicit formulas for determining the properties of the bifurcating periodic solutions by applying the center manifold theory and normal form method. In Section 3, we give the sufficient conditions for the occurrence of the Turing–Hopf bifurcation. In Section 4, to illustrate the complex dynamics of system (4), we calculate the normal form near the Turing–Hopf bifurcation point. In Section 5, we give some numerical simulations to illustrate our theoretical results.
2. Dynamics of the ODE Model
When diffusion is absent, system (4) becomes
It is easy to see that system (5) always has three boundary equilibria: . Obviously, the interior equilibria should satisfy the following equation
which yields to
Therefore, when the following condition
is satisfied, system has two interior equilibria and , where , and
Then, we analyze the stability of all equilibria of system (5). Note that the Jacobian matrix cannot be evaluated at since is not differentiable at . We can obtain, from the first equation of (5), that
Similarly, from the second equation of system (5), we have that
which means and when , . From the equation for the prey density, we have for ,
where , . It can be proven that , thus . Notice that
so we mainly consider two cases:
Case I: If has infinite extremum for , then the maximal values are determined by , which can be given by
Since , we can obtain that .
Case II: If has finite extremum when , then there exists a such that is a monotonic function of t when . Notice that , we have . Therefore, is monotonically decreasing for , and we claim that . Otherwise, . Then, for any , we have
for a sufficiently large t. It is easy to prove that
which implies that when . It contradicts the assumption . Consequently, . Based on the above discussion, we obtain that is locally asymptotically stable. For , the corresponding Jacobian matrix can be given by
respectively, so we can obtain the local stability of boundary equilibria as follows.
Lemma 1.
- (i)
- is a stable node;
- (ii)
- If , then is a source, and is a saddle;
- (iii)
- If , then is a saddle, and is a stable node.
Next, we analyze the local stability of . The Jacobian Matrices around can be written as
and
According to Equations (7) and (10), we can conclude that
which implies that is always a saddle, and the stability of is determined by the sign of . Substituting the expressions for and , we have
When holds, we can obtain that
Note that , we obtain that
provided . So, under the assumptions and , (11) has a unique positive zero such that when , while when . Denote
Summarizing the previous discussion, we conclude that:
Theorem 1.
- (i)
- is unstable;
- (ii)
- If holds, then there exists a unique such that is asymptotically stable when , while is unstable when , where is the positive zero of (11).
In fact, we can also obtain the conclusion as follows.
Lemma 2.
Proof.
Denote
where
Let be a pair of complex roots of
satisfying . Then,
Since
we complete the proof. □
Let , . For the sake of convenience, we still denote and by u and v. Thus, system can be rewritten as
Rewrite system as
where
with
Let
where
Then, we obtain that
Denote
Using , system (15) becomes
where
The polar coordinate form of (16) can be written as:
By Taylor expanding (17) at , we have
To determine the stability of the bifurcating periodic solutions, we need to discuss the sign of , which is given by
where all partial derivatives are evaluated at the bifurcation point , and
Thus, we can obtain the sign of the coefficient in . Note that ; we draw the following conclusions.
Theorem 2.
Suppose that and hold. Then, system (5) undergoes a Hopf bifurcation at when . Furthermore:
- (i)
- If , the bifurcating periodic solutions are orbitally asymptotically stable, and periodic solutions occur as h decreases and passes .
- (ii)
- If , the bifurcating periodic solutions are unstable, and periodic solutions occur as h decreases and passes .
3. Turing Instability Induced by Diffusion and Turing–Hopf Bifurcation
In this section, we discuss the effect of diffusion on the stability of and give the sufficient conditions for the occurrence of Turing instability induced by diffusion. By computation, we have that the characteristic equations corresponding to can be given by
which can be equivalent to
where
with defined as in (13). In the following analysis, we always assume that and are satisfied.
Theorem 3.
Assume that and hold. Then, there exists a positive integer , for :
- (i)
- (ii)
- The Turing–Hopf bifurcation occurs at when , where
Proof.
From Theorem 1, we know that Turing instability occurs as has roots with a positive real part for some when . From , can be satisfied provided . Thus, we only need to seek the condition for to ensure the occurrence of Turing instability. In fact, is equivalent to
By calculation, we have
where is a function of h defined as in (7). Since , , we have . Then, is a monotonically decreasing function with respect to h. Notice that
Thus, if and only if holds true. Denote
we can conclude that for . To guarantee the positiveness of on the curve , we should ensure that the condition holds. Denote the Turing bifurcation curve as , that is
When intersects the critical Hopf bifurcation curve at , system undergoes the Turing–Hopf bifurcation at as
For , to seek the maximum of , we take the derivative of with respect to . We can have that
In fact, has the same sign as
when holds. Let . We can see that
So, there must exist a satisfying and as , while as . Denote . As , is a decreasing function of n. As , is increasing for and decreasing for . So, will reach the maximum value as , , or . Let
we can obtain that . Then, we complete the proof. □
4. Normal Forms for Turing–Hopf Bifurcation
Denote
and drop the bars. Then, we can rewrite as follows:
By setting and , is the Turning-Hopf singularity in the plane. Thus, system becomes
where
It follows from that for , when , has a pair of purely imaginary roots with , has a zero root and a negative real root , and, if , all of the roots of have negative real parts. For , we have
and
For convenience, we rewrite and as
For L, we have
with
Let
By calculation, we obtain that
where
with
Following the techniques in [35], by a recursive transformation, we can obtain that the normal form for the Turing–Hopf bifurcation can be given by
where
and
Next, we need to calculate , , and .
with
Then, we can figure out by calculation that
Thus, we can obtain
with
and
So, the normal form truncated to the third-order terms for the Turing–Hopf bifurcation can be written as
where
5. Numerical Simulations
In this section, we provide some numerical simulations to show the previous analysis.
To illustrate Theorem 2, we choose , , , , and such that and hold. By calculation, we have , , and . According to Theorem 2, we know that (5) undergoes a Hopf bifurcation at when h decreases and passes , and the bifurcating periodic solutions are stable, as shown in Figure 1.
Figure 1.
System (5) has stable periodic solutions. (a) represents the prey u, and (b) represents the predator v.
Choose , such that and hold. We can obtain, from Theorem 3, that the Turing–Hopf bifurcation occurs at and the wave number is (see Figure 2). When , . By calculation, the normal form truncated to the third-order term is
Recalling that , system (28) has the equilibria
Figure 2.
Stable region for in plane on region as , .
- ,
- , for ,
- , for ,
- ,
for .
Denote the bifurcation curves as
Then, we obtain the bifurcation diagram in the plane and the corresponding phase portraits of system (28) in the plane, as shown in Figure 3. Clearly, the above curves divide the plane into six regions, denoted as (see Figure 3). The existence and stability properties of the steady states in the six regions are listed in Table 1.
Figure 3.
(a) Detailed parameter regions near the Turing–Hopf bifurcation point ; (b) phase portraits in region .
Table 1.
Stability of the steady states in different regions of system (28).
Obviously, the equilibria , , , and of system (28) correspond to the constant equilibrium, the spatially homogeneous periodic solution, the nonconstant steady state, and the spatially inhomogeneous periodic solution of system (4). Thus, the dynamical behaviors of system (4) nearby the Turing–Hopf singularity in the plane can be determined by the dynamical behaviors of system (28).

Figure 4.
When = (0.0005, 0.001) lies in , is locally asymptotically stable. (a,b) represent the prey u, and (c,d) represent the predator v. The initial values are chosen as , . (b,d) are middle-term behaviors for u and v, respectively.
In , there are two equilibria, and in (28). Since is stable, system (4) has a stable, spatially homogeneous periodic solution; see Figure 5.
Figure 5.
When = (−0.00001, 0.1) lies in , system (4) has stable, spatially homogeneous period solutions. (a,b) represent the prey u, and (c,d) represent the predator v. The initial values are chosen as , . (b,d) are long-term behaviors for u and v, respectively.
In , there are four equilibria, , , and in (28). Since and are stable, there exist spatially inhomogeneous periodic solutions; see Figure 6.
Figure 6.
When = (−0.000003, 0.0004) lies in , system (4) has two spatially inhomogeneous periodic solutions. (a,b,e,f) represent the prey u, and (c,d,g,h) represent the predator v. The initial values are and in (a,d) and and in (e,f). (b,d,f,h) are long-term behaviors for u and v, respectively.
In , there are six equilibria, , , , and , in (28). Since and are stable, there exist spatially inhomogeneous periodic solutions; see Figure 7.
Figure 7.
When = (−0.000003, 0) lies in , system (4) has two spatially inhomogeneous periodic solutions. (a,b,e,f) represent the prey u, and (c,d,g,h) represent the predator v. The initial values are and in (a,d) and and in (e,f). (b,d,f,h) are long-term behaviors for u and v, respectively.
In , there are four equilibria, , , and , in (28). Since and are stable, there exist spatially inhomogeneous steady states; see Figure 8.
Figure 8.
When = (−0.000003, −0.1) lies in , system (4) has spatially inhomogeneous steady states. (a,b) represent the prey u, and (c,d) represent the predator v. The initial values are chosen as and in (a–d). (b,d) are long-term behaviors for u and v, respectively.
In , there are three equilibria, and , in (28). Since and are stable, there exist spatially inhomogeneous steady states; see Figure 9.

Figure 9.
When = (−0.0001, 0.04) lies in , system (4) has spatially inhomogeneous steady states. (a,b) represent the prey u, and (c,d) represent the predator v. The initial values are chosen as and . (b,d) are long-term behaviors for u and v, respectively.
6. Conclusions and Discussion
In this paper, we investigate the ratio-dependent predator–prey system with the Allee effect in prey and predator harvesting. We give a detailed analysis of the joint effect of harvesting effort and diffusion on the spatiotemporal behaviors of system (4), and our results reveal that the presence of a harvesting term makes the system exhibit more interesting dynamical behaviors.
A ratio-dependent predator–prey system with a harvesting term is a relatively new issue that has been investigated by several researchers and has yielded many interesting results. Recently, Gao et al. [34] analyzed the existence of a Hopf bifurcation induced by harvesting rate and a Turing bifurcation induced by diffusion, respectively, for systems (4) without the Allee effect. However, they did not consider the dynamics of multi-parameter synergism, which is also a major difficulty in our research.
The main contribution of our paper is a detailed analysis of bifurcation near the positive constant steady state of system (4) in the one-dimensional spatial domain . For the spatially homogeneous model, using the harvesting rate h as the bifurcation parameter, we analyze the stability of interior equilibria. By applying the center manifold theory and normal form method, we derive the formula determining the direction of the Hopf bifurcation and the stability of the bifurcating periodic solutions. For the reaction–diffusion model, we firstly verify the existence of Turing instability induced by diffusion, which reveals the existence of spatially inhomogeneous patterns, including the spatially inhomogeneous periodic solutions and non-constant steady-state solutions. Then, the normal form near the Turing–Hopf bifurcation point is derived. Our study demonstrates that as the harvesting rate h decreases and passes the critical value , the coexistence equilibrium will lose its stability, and the Hopf bifurcation occurs. Finally, numerical simulations, which are consistent with the theoretical results, are performed to illustrate the theoretical analysis.
In ecosystems, humans, as higher animals, have the ability to harvest biological resources. Our research shows that if humans overharvest biological resources, it will lead to the unbalance of the ecosystem. Our study provides the critical harvesting rate without destroying the ecosystem, which not only ensures the health of the ecosystem but also maximizes the biological resources available to humans. At the same time, our results also show that humans can obtain better harvest times and easier harvest locations by controlling the ratio of the diffusion coefficients of prey and predators and the harvesting rate near the Turing–Hopf singularity . This can greatly reduce the difficulty for humans in obtaining biological resources.
In [36], the authors proposed the non-continuous harvesting function as follows
They assumed that the harvesting may start as the population reaches some critical value T. To further the study, we will consider a non-continuous harvesting function in our system, compare the theoretical results to the results in the paper, and reveal the effect of the harvesting rate on the predator population. Moreover, we may consider the effect of spatial heterogeneity on the dynamics of (4).
Author Contributions
Methodology, J.Z.; Writing—original draft, M.C.; Writing—review & editing, Y.X.; Supervision, X.W. All authors have read and agreed to the published version of the manuscript.
Funding
This research is supported by the National Natural Science Foundation of China (No. 11901172) and the Fundamental Research Funds for the Universities in Heilongjiang Province (Nos. 2022-KYYWF-1043, 2021-KYYWF-0017).
Data Availability Statement
The data presented in this study are available on request from the corresponding author.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
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