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ORIGINAL RESEARCH article

Front. Phys., 19 June 2024
Sec. Social Physics

Bifurcation analysis of a Leslie-type predator–prey system with prey harvesting and group defense

Yongxin ZhangYongxin ZhangJianfeng Luo
Jianfeng Luo*
  • School of Mathematics, North University of China, Taiyuan, China

In this paper, we investigate a Leslie-type predator–prey model that incorporates prey harvesting and group defense, leading to a modified functional response. Our analysis focuses on the existence and stability of the system’s equilibria, which are essential for the coexistence of predator and prey populations and the maintenance of ecological balance. We identify the maximum sustainable yield, a critical factor for achieving this balance. Through a thorough examination of positive equilibrium stability, we determine the conditions and initial values that promote the survival of both species. We delve into the system’s dynamics by analyzing saddle-node and Hopf bifurcations, which are crucial for understanding the system transitions between various states. To evaluate the stability of the Hopf bifurcation, we calculate the first Lyapunov exponent and offer a quantitative assessment of the system’s stability. Furthermore, we explore the Bogdanov–Takens (BT) bifurcation, a co-dimension 2 scenario, by employing a universal unfolding technique near the cusp point. This method simplifies the complex dynamics and reveals the conditions that trigger such bifurcations. To substantiate our theoretical findings, we conduct numerical simulations, which serve as a practical validation of the model predictions. These simulations not only confirm the theoretical results but also showcase the potential of the model for predicting real-world ecological scenarios. This in-depth analysis contributes to a nuanced understanding of the dynamics within predator–prey interactions and advances the field of ecological modeling.

1 Introduction

Since the pioneering work of Lotka and Volterra, who introduced a pair of differential equations to describe predator–prey dynamics, predator–prey models have attracted considerable interest from both mathematicians and biologists due to their widespread applicability [1]. Predominantly, predator–prey models have been developed around two main scenarios: (i) the growth function of the predator is directly proportional to its predation function, capturing the functional response of predators to prey availability, and (ii) the growth function of the predator is decoupled from its predation function, suggesting a more intricate relationship between the predator and prey.

Moreover, the growth term of the predator in these models is often portrayed as a function that depends not only on prey density but also on the predator-to-prey ratio, adding another dimension of complexity to the interactions. Among these diverse models, the Leslie-type model has emerged as a particularly influential paradigm. Its sophisticated treatment of predator–prey interactions has solidified its role as a fundamental framework in ecological studies, aiding in the comprehension of the delicate equilibrium within ecosystems.

[2] proposed a Leslie-type model to describe the relationship between predators and their prey:

dxdt=rx1xKyfx,dydt=qy1ypx,

where x and y denote the population densities of the prey and predators, respectively. In the absence of predators, the growth of prey populations is commonly modeled using a logistic growth function, characterized by an intrinsic growth rate r and an environmental carrying capacity K. This model assumes that population growth is limited by the availability of resources as the population size approaches the carrying capacity. The functional response, represented by f(x), describes how the rate of prey consumption by predators varies with the density of the prey population. In contrast, the growth rate of the predator is a Leslie-type growth function expressed as q(1ypx), which depends on both the prey density and the predator density. Here, q denotes the intrinsic per capita growth rate of the predator in the presence of abundant prey, p is a scaling factor that relates the carrying capacity of the predator to that of the prey, and the term 1ypx reflects the diminishing growth rate as the predator-to-prey ratio approaches one, indicating prey scarcity. This growth function is particularly useful for simulating systems where the success of the predator in capturing the prey is influenced not only by prey abundance but also by the density of the predator population. It captures the competitive pressures and the complex dynamics of resource allocation within an ecosystem, offering a more nuanced understanding of predator–prey interactions. The functional response function f(x) is typically categorized into four classical types: Holling type I [3], Holling type II [4], Holling type III [5, 6], and Holling type IV [7, 8]. These types are defined by specific mathematical expressions that reflect different assumptions about predator behavior and the efficiency of predation. Most predator–prey models incorporate one of these functional responses or their modifications.

Recently, [9, 10] proposed a novel functional response model that replaces the traditional prey density with the square root of prey density in the context of the Holling type II functional response. This innovation is particularly pertinent for prey species that exhibit herding behavior, where only peripheral individuals engage with predators. This revised functional response more accurately reflects how the protective effects of group living affect the rate at which predators encounter and consume the prey. Combining their functional response functions, we propose the following Leslie-type model:

dxdt=rx1xKαxy1+Thαx,dydt=qy1ypx,(1)

where α presents the search efficiency of the predator for the prey and Th denotes the average handing time for each prey.

Before going into details, by substituting

x̄=xK,ȳ=αyrK,t̄=rt,a=ThαK,b=qr,d=rpαK,

into model Eq. 1 and dropping the bars, we obtain

dxdt=x1xxy1+ax,dydt=by1dyx.(2)

Over the past three decades, a considerable amount of research has been devoted to understanding the effects of harvesting on the dynamics of predator–prey systems and its implications for the management of renewable resources. [11] explored a predator–prey model that includes Michaelis–Menten-type predator harvesting. In a similar vein, [12] discussed a modified Leslie–Gower model incorporating Michaelis–Menten-type prey harvesting. [13] investigated a model where both predator and prey populations exhibit logistic growth and are subject to nonlinear harvesting. The impact of proportional harvesting on the dynamic behavior of predator–prey models was examined by [14, 15]. [16] provided a detailed bifurcation analysis for a model with Holling-type II functional response and a constant harvesting rate. [17] also studied a model with constant prey harvesting. [18, 19] studied the dynamic behaviors of the predator–prey systems with a Holling- and Leslie-type or Leslie–Gower model with constant-yield prey harvesting, revealing a diverse array of bifurcations. [20] and [21] discussed ratio-dependent predator–prey systems with constant harvesting for both prey and predators, respectively. [22] investigated a system where the prey population forms herds as a defense against predators, and both species are exposed to a constant harvesting rate.

Inspired by these studies, we introduce the impact of a constant harvesting rate for the prey into Eq. 2 and obtain the following results:

dxdt=x1xxy1+axh,dydt=by1dyx,(3)

where h represents the rate of prey harvesting.

It should be noted that system Eq. 2 is a Leslie-type predator–prey model that incorporates prey group defense mechanisms. Furthermore, system Eq. 3 extends this framework by accounting for the constant harvesting of the prey within system Eq. 2. To date, the dynamic behaviors of both systems Eq. 2 and Eq. 3 remain unexplored. Given the significance of biological resources as a sustainable source for human utilization and considering the rapid industrialization and population growth that have led to an inevitable increase in the utilization of various biological assets, it is imperative to investigate the impact of harvesting behavior on the population of both the predator and prey, particularly when prey group defense is involved, for the sake of maintaining ecological balance. In this paper, we study the dynamic behaviors of these two systems. Through rigorous mathematical analysis, we find that the population of the prey will be sustained without the effect of prey harvesting. However, due to the emergence of prey harvesting, system Eq. 3 exhibits complex dynamic behaviors and undergoes saddle-node, Hopf, and Bogdanov–Takens (BT) bifurcations. System Eq. 3 has bi-stable behavior due to saddle-node bifurcation, and whether the prey becomes extinct or not depends on the prey harvesting intensity. Specifically, we determine the maximum sustainable yield as hMSY=14. Once the prey harvesting rate h exceeds hMSY, both the prey and predator species face extinction. This insight underscores the importance of selecting an appropriate harvesting rate, specifically to ensure the co-existence of the predator and prey, thereby sustaining ecological balance.

The structure of this paper is shown in Figure 1. Section 2 discusses the existence and stability of the equilibria for system Eq. 2. Section 3 delves into the investigation of the equilibria for system Eq. 3, providing both analytical insights and corroborating numerical results. Section 4 focuses on the bifurcation analysis of system Eq. 3, examining both saddle-node and Hopf bifurcations. Additionally, this section explores the Bogdanov–Takens bifurcation within the same system. Concluding remarks are given in Section 5, summarizing the key findings and implications of the study.

Figure 1
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Figure 1. Flowchart of studies of the prey–predator system focusing on the harvesting setting in this paper.

2 Equilibria of system (3)

2.1 Existence of equilibria

To determine the equilibria of system Eq. 2, we analyze the prey and predator nullclines, which are given by the following equations:

x1xxy1+ax=0,by1dyx=0.

From these nullclines, it is evident that system Eq. 2 has a unique boundary equilibrium at E00=(1,0). To identify potential positive equilibria, we solve the following equations:

fx1xxd1+ax=0,yxd.

By substituting x=z, we transform the problem of finding positive solutions to f(x) = 0 into finding positive solutions to g(z) = adz3 + dz2 + (1 − ad)zd = 0. Through algebraic analysis, we can easily determine that g(z) = 0 has a unique positive solution. Consequently, system Eq. 2 has a unique positive equilibrium point, denoted as E0*=(x0*,y0*), where y0*=x0*d, x0*=z02, and z0 is the unique positive root of g(z) = 0. Based on this analysis, we can formulate the following theorem regarding the number of equilibria in system Eq. 2.

Theorem 2.1. System Eq. 2 possesses a unique boundary equilibrium E00=(1,0) and unique positive equilibrium denoted by E0*=(x0*,y0*).

2.2 Stability of equilibria

Theorem 2.2. For all positive parameters, system Eq. 2 has a boundary equilibrium E00 and a positive equilibrium E0*. Moreover, the boundary equilibrium E00 is always a hyperbolic saddle. Furthermore, the positive equilibrium E0* is a sink when b > b0, a source when b < b0, or a center when b = b0, where b0=1z02z02d(1+az0)2 and z0 is the positive root of g(z) = 0.

Proof. The Jacobian matrix of system Eq. 2 evaluated at E00 is given by

JE00=111+a0b.

It is obvious that the matrix J(E00) has a positive eigenvalue b and a negative eigenvalue −1. Therefore, E00 is always a hyperbolic saddle.

The Jacobian matrix of system Eq. 2 evaluated at E0* is given by

JE0*=12x0*x0*2d1+ax0*2x0*1+ax0*bdb=12z02z02d1+az02z01+az0bdb.

According to g(z0) = 0, we can obtain 1z02=z0d(1+az0). Then,

DetJE0*=bz02+bz02d1+az02>0,TrJE0*=1z02z02d1+az02bb0b.

Hence, when b > b0, Tr[J(E0*)]<0, the matrix J(E0*) has two negative part eigenvalues, and E0* is a sink. When b < b0, then Tr[J(E0*)]>0, the matrix J(E0*) has two positive part eigenvalues, and E0* is a source. When b = b0, then Tr[J(E0*)]=0, the matrix J(E0*) has a pair of purely imaginary eigenvalues, and E0* is a center.

3 Equilibria of system (4)

3.1 Existence of equilibria

This section conducts a qualitative analysis of model Eq. 3. With the biological context in mind, we focus on examining the dynamics of system Eq. 3 within the closed first quadrant, denoted as R+2, in the (x, y) coordinate plane.

In order to obtain the equilibria of system Eq. 3, we first study the roots of the following equations:

x1xxy1+axh=0,by1dyx=0.(4)

Regarding the count of boundary equilibria for system Eq. 3, we derived the subsequent theorem.

Theorem 3.1. (i) When h=14, system Eq. 3 admits a unique boundary equilibrium E0=(12,0).

(ii) When 0<h<14, system Eq. 3 admits two boundary equilibria Ei = (xi, 0) (i = 1, 2), where x1=114h2 and x2=1+14h2.

Proof. When h exceeds 14, ẋ=x(1x)hxy1+ax<0. This implies that the dynamics of system Eq. 3 within R+2 are inherently trivial. Consequently, the prey species faces extinction, an event that subsequently triggers the extinction of the predator. It is evident that system Eq. 3 lacks any equilibrium points within the positive quadrant R+2.

We next explore the existence of boundary equilibria under the condition that h14. Specifically, when y = 0 in Eq. 4, we are confronted with the following equation:

x2xh=0.(5)

It is straightforward to determine that when h<14, Eq. 5 has two distinct roots, denoted as x1 and x2. Conversely, when h=14, the equation yields a unique root, which is 12.

Note that

f1zadz5+dz4+1adz3dz2+adhz+hd,g1zf1z=5adz4+4dz3+31adz22dz+adh,h1zg1z=20adz3+12dz2+61adz2d.(6)

Regarding the positive equilibria of system Eq. 3, we have the following theorem.

Theorem 3.2. (i) When h=h2* and h2*<h1*, system Eq. 3 has a unique positive equilibrium E3 = (x3, y3).

(ii) When h<min{h1*,h2*}, system (4) has two different positive equilibria Ei = (xi, yi) (i = 4, 5),

where h1*=5az14+2z13+z1a, h2*=z32(2az33+z32+1)2az3+3, z3 is the larger positive root between two positive roots of g1(z) = 0, and z1 is the only positive root of h1(z) = 0.

Proof. When y ≠ 0, then y=xd according to Eq. 5, and x is the positive root of the equation

x1x1+axdxxdh1+ax=f1z,

where z=x and f1(z) is given in Eq. 6.

Through algebraic analysis, we find that the equation h1(z) = 0 has a unique positive root, denoted as z1. When g1(z1) < 0, which corresponds to h<h1*5az14+2z13+z1a, the equation g1(z) = 0 admits two distinct positive roots, z2 and z3 (with z2 < z3). If f1(z3) = 0, which occurs when h=h2*z32(2az33+z32+1)2az3+3, then the equation f1(z) = 0 has a unique positive root. Consequently, system Eq. 3 admits a unique positive equilibrium E3 = (x3, y3), where x3=z32 and y3=x3d. If f1(z3) < 0, corresponding to h<h2*, then the equation f1(z) = 0 has two distinct positive roots, z4 and z5 (with z2 < z4 < z3 < z5). In this case, system Eq. 3 has two distinct positive equilibria, E4 = (x4, y4) and E5 = (x5, y5), where x4=z42, x5=z52, y4=x4d, and y5=x5d.

3.2 Stability of equilibrium E0

Theorem 3.3. When h=14, system Eq. 3 possesses a unique boundary equilibrium at E0=(12,0), which is classified as a saddle-node. This equilibrium divides a sufficiently small neighborhood into two parts, separated by two separatrices that approach E0 from above and below. One part forms a parabolic sector, while the other comprises two hyperbolic sectors. Additionally, the parabolic sector is situated in the left half-plane, and the equilibrium E0 acts as a repelling saddle-node. The dynamics of the system in this scenario are illustrated in the phase portraits shown in Figure 2A.

Figure 2
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Figure 2. (A) Phase portrait of system (4) with a = 0.4, b = 0.5, d = 0.6, and h=14. (B) Phase portrait of system (4) with a = 0.4, b = 0.5193087015, d = 0.6, and h = 0.04485055324. E1 is an unstable node, E2 is a saddle, and E3 is a cusp.

Proof. The Jacobian matrix J(E0) of system Eq. 3 evaluated at E0 is

JE0=012+a0b.

Given that Det[J(E0)] = 0, we can conclude that the equilibrium (12,0) is nonhyperbolic, indicating that it is a degenerate equilibrium. It is evident that the eigenvalues of the Jacobian matrix J(E0) are λ1 = 0 and λ2 = b. To ascertain the stability of E0, we perform a transformation by shifting the equilibrium to the origin using the transformation (X,Y)=(x12,y). We then expand system Eq. 3 in a power series up to the second order around the origin. Under this transformation, system Eq. 3 becomes

Ẋ=12+aYX222+a2XY+P1X,Y,Ẏ=bY2bdY2+Q1X,Y,

where P1(X, Y) and Q1(X, Y) are smooth functions of at least the third order with respect to (X, Y).

Then, making the transformation

XY=112+a0bxy,

and introducing a new time variable τ = bt, for which we retain t to denote τ for notational simplicity, we obtain

ẋ=a20x2+a11xy+a02y2+P2x,y,ẏ=y2bdy2+Q2x,y,

where P2(x, y) and Q2(x, y) are smooth functions of at least the third order with respect to (x, y) and

a20=a5+52a4+20a3+202a2+20a+42a+25b<0,a11=2a42b+8a3+64ba2223b8a+42ba+25b,a02=2a2b2da2+42a+12+a2a2b+32+a16b2d+64b+8b2d22b+22a+25b.

According to Theorem 7.1 from Chapter 2 in [23], the equilibrium E0 is classified as a saddle-node. This implies that the vicinity of E0 is bifurcated by two separatrices that approach E0 from above and below. One region forms a parabolic sector, while the other comprises two hyperbolic sectors. Additionally, the parabolic sector is situated in the right half-plane, and E0 acts as a repelling saddle-node.

3.3 Stability of equilibria E1 and E2

Theorem 3.4. When 0<h<14, system Eq. 3 has two different boundary equilibria E1 and E2. Moreover, E1 is always a hyperbolic unstable node, and E2 is always a hyperbolic saddle. The corresponding phase portraits are shown in Figure 2B and Figure 3.

Figure 3
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Figure 3. (A) Phase portrait of system (4) with a = 0.4, b = 0.2, d = 0.6, and h = 0.04485055324. E1 is an unstable node, E2 is a saddle, and E3 is a repelling saddle node. (B) Phase portrait of system (4) with a = 0.4, b = 1.2, d = 0.6, and h = 0.04485055324. E1 is an unstable node, E2 is a saddle, and E3 is an attracting saddle node.

Proof. The Jacobian matrix J(E1) of system Eq. 3 evaluated at E1 is

JE1=14hx11+ax10b.

We can obtain that the eigenvalues are λ1=14h>0 and λ2 = b > 0. Hence, E1 is a hyperbolic unstable node.

The Jacobian matrix J(E2) of system Eq. 3 evaluated at E2 is

JE2=14hx21+ax20b.

It is easy to observe that the eigenvalues are λ1=14h<0 and λ2 = b > 0. Hence, E2 is a hyperbolic saddle.

3.4 Stability of equilibrium E3

Now, we investigate the stability of equilibrium E3. The Jacobian matrix J(E3) of system Eq. 3 evaluated at E3 is

JE3=12x3x32d1+ax32x31+ax3bdba10a01b10b01.

Straightforward computation shows that, due to x3=z32,

DetJE3=b2d1+az32lz3,

where

lz=4a2dz4+8adz3+2a+4d2a2dz2+34adz2d.

Since f(z3) = 0, from Theorem 3.2, we can obtain

h=z32adz33+dz32+1adz3dd1+az3.

Substituting g1(z3) in the above equation yields g1(z3)=z31+az3l(z3). Because z3 is a positive root of g1(z) = 0, g1(z3) = 0 and l(z3) = 0. Therefore, Det[J(E3)] = 0. Therefore, we can establish that equilibrium E3 is nonhyperbolic, which means it is a degenerate equilibrium. To elaborate further, we present the following theorem:

Theorem 3.5. (i) If a10+b010(bb1*12x3x32d(1+ax3)2),

(i-1) a10+b01<0(b>b1*), then the parabolic sector is located in the right half-plane, and E3 is an attracting saddle-node. The corresponding phase portrait is shown in Figure 3B.

(i-2) a10+b01>0(b<b1*), then the parabolic sector is located in the left half-plane, and E3 is a repelling saddle-node. The corresponding phase portrait is shown in Figure 3A.

(ii) When a10+b01=0(b=b1*), E3 represents a degenerate critical point, specifically a cusp. Furthermore, E3 is a cusp of co-dimension 2 under the condition that dd1* and dd2*. However, if d=d1* or d=d2*, E3 is a cusp of co-dimension at least 3. The corresponding phase portraits are shown in Figure 2B,where d1*=4ax3+(3a4)x3+18x3(1+ax3)3 and d2*=6x3(1+ax3)+3ax3+18(1+ax3)3(23x3).

Proof. Since Tr[J(E3)] = a10 + b01, we know that the eigenvalues of J(E3) are λ1 = 0 and λ2 = a10 + b01.

Similar to the proof outlined in Theorem 3.3, we perform a transformation that shifts equilibrium E3 to the origin. We then expand system Eq. 3 in a power series up to the second order around this new origin. This transformation yields a simplified system that

Ẋ=a10X+a01Y+a11XY+a20X2+P11X,Y,Ẏ=b10X+b01Y+b11XY+b20X2++b02Y2+Q11X,Y,(7)

where P11(X, Y) and Q11(X, Y) are smooth functions of at least the third order with respect to (X, Y), and

a11=12x31+ax32,a20=1+3ax38dx31+ax331,
b11=2bx3,b20=bdx3,b02=bdx3.

When a10 + b01 ≠ 0, J(E3) has one zero eigenvalue and a nonzero eigenvalue. To further analyze the stability of this equilibrium, we introduce a transformation that

XY=1a10b10a10a011xy,

and introducing a new time variable τ1 = (a10 + b01)t, for which we retain t to denote τ1 for notational simplicity, we obtain

ẋ=c20x2+c11xy+c02y2+P21x,y,ẏ=y+d20x2+d11xy+d02y2+Q21x,y,

where P21(x, y) and Q21(x, y) are smooth functions of at least the third order with respect to (x, y), and

c20=1a10+b012a01a11b02+a10a01a20b11b10a102a01b20b102,
c11=1a10+b012a11b01a10a112b022b01b20a102b102+b11a102+2a10b01a2012b11b10,c02=1a10+b012a10b11a01b20+a20b01a11b10a10b10b02b01,d20=1a10+b012b01b20+b10a20b11b102a11b02b01,d11=1a10+b0122a01b20+b01b11+a112b02b10+2a20b11a10a10a11b10b01,d02=1a10+b012a10a11+b01b02+a01b11+a102a20+a10a01b20b10.

Straightforward computation shows that

c20=ba10+b0123a2dx332+a8+dx3+a3dx32+3adx3+38dx3a+ax33>0.

Consequently, as shown by Theorem 7.1 from Chapter 2 in [23], if a10 + b01 ≠ 0, then the equilibrium E3 qualifies as a saddle-node. Moreover, the characteristics of this saddle-node are determined as follows: (i) if a10 + b01 > 0, the parabolic sector is situated in the upper half-plane, and E3 acts as a repelling saddle-node and (ii) conversely, if a10 + b01 < 0, the parabolic sector remains in the upper half-plane, but E3 is an attracting saddle-node.

When a10 + b01 = 0, J(E3) has one zero eigenvalue with two multiple. Then, making the transformation

XY=11a10a010xy,

and introducing a new time variable τ2 = −b01t = bt. For notational simplicity, we retain t to represent τ2, then system Eq. 7 becomes

ẋ=y+e02y2+P22x,y,ẏ=f20x2+f11xy+f02y2+Q22x,y,(8)

where P22(x, y) and Q22(x, y) are smooth functions of at least the third order with respect to (x, y) and

e02=1x3,f20=a11bd+a20b,f11=2a20b+a11bd4x3,f02=a20b+1x3.

To eliminate y2 terms in system Eq. 8, we make the following near identity transformation:

x=X+f022X2,y=Y+f02XYe02Y2,

which transforms system Eq. 8 into

Ẋ=Y+P23X,Y,Ẏ=f20X2+f11XY+Q23X,Y,

where P23(X, Y) and Q23(X, Y) are smooth functions of at least the third order with respect to (X, Y). Therefore, when f20 ≠ 0 (dd1*=4ax3+(3a4)x3+18x3(1+ax3)3) and f11 ≠ 0 (dd2*=6x3(1+ax3)+3ax3+18(1+ax3)3(23x3)), according to the results presented by [24], E3 is a cusp of co-dimension 2. If f20=0(d=d1*) or f11 = 0 (d=d2*), E3 is a cusp of co-dimension at least 3.

3.5 Stability of equilibria E4 and E5

Theorem 3.6. When system Eq. 3 exists with two positive equilibria E4 and E5, E4 is always a hyperbolic saddle. Furthermore, positive equilibrium E5 is a sink when b > b*, a source when b < b*, or a center when b = b*, where b*=12z52z52d(1+az5)2 and z5 is the larger positive root of f1(z) = 0.

Proof. The Jacobian matrix J(E4) of system Eq. 3 evaluated at E4 is

JE4=12x4x42d1+ax42x41+ax4bdb.

Straightforward computation shows that, due to x4=z42,

DetJE4=b2d1+az42lz4,

where

lz=4a2dz4+8adz3+2a+4d2a2dz2+34adz2d.

Since f(z4) = 0, from Theorem 3.2, we obtain

h=z42adz43+dz42+1adz4dd1+az4.

Substituting g1(z4) by the above equation, then g1(z4)=z41+az4l(z4). Because z2 < z4 < z3, z2 and z3 are two positive roots of g1(z) = 0, then g1(z4) < 0 and l(z4) < 0. Therefore, Det[J(E4)] < 0. Hence, the matrix J(E4) has a positive eigenvalue and a negative eigenvalue. Hence, E4 is a hyperbolic saddle.

Similarly, we obtain

DetJE5=b2d1+az52lz5>0,

since l(z5) > 0 (z5 > z3). Moreover, we can also obtain

TrJE5=12x5x52d1+ax52bb*b.

Hence, when b > b*, Tr[J(E5)] < 0, the matrix J(E5) has two negative part eigenvalues, and E5 is a sink. When b < b*, then Tr[J(E5)] > 0, the matrix J(E5) has two positive part eigenvalues, and E5 is a source. When b = b*, then Tr[J(E5)] = 0, the matrix J(E5) has a pair of pure imaginary eigenvalues, and E5 is a center.

4 Bifurcation analysis

In this section, we investigate the bifurcations that take place in system Eq. 3.

4.1 Saddle-node bifurcation

According to Theorem 3.1, we provided the conditions for the existence of E1 and E2 based on some restrictions. We obtain that

SN1=a,b,d,h:h=14,a>0,b>0,d>0

is a saddle-node bifurcation surface. Consequently, we can deduce that on the surface SN1, system Eq. 3 possesses a unique equilibrium E0, which is a saddle-node. As the parameters traverse this surface, the quantity of boundary equilibria undergoes a transition from zero to two. Biologically, this bifurcation corresponds to a critical threshold where the maximum sustainable yield (MSY) is at hMSY=14. Beyond this threshold (h>14), the prey species faces extinction, leading to the collapse of the system. However, under certain initial conditions where 0<h<14, the prey species can avoid extinction [18, 20]. This phenomenon is shown in the saddle-node bifurcation diagram, as shown in Figure 4B.

Figure 4
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Figure 4. (A) Saddle-node bifurcation diagram SN2 with a = 0.4, d = 0.6, and b = 0.5, where H represents the Hopf bifurcation point. The solid curve represents the stable equilibrium, and the dotted curve stands for the unstable equilibrium. (B) Saddle-node bifurcation diagram SN1 with a = 0.4, d = 0.6, and b = 0.5.

Similar to the above discussion, we obtain

SN2=a,b,d,h:h=h2*,h2*<h1*,a>0,b>0,d>0,

according to Theorem 3.2, is another saddle-node bifurcation surface. When the parameters transition from one side of the surface to the other, the number of positive equilibria in system Eq. 3 changes from zero to two. The saddle-node bifurcation is illustrated in Figure 4A.

4.2 Hopf bifurcation

From Theorem 3.6, we know that the positive equilibrium E5 is a center-type nonhyperbolic equilibrium when b = b* and h<min{h1*,h2*}. Therefore, system (4) may undergo a Hopf bifurcation. To proceed, we first confirm the transversality condition necessary for a Hopf bifurcation,

ddbTrJE5|b=b*=10.

Therefore, the stability of the positive equilibrium E5 undergoes a change as the parameters traverse the specific critical surface

H1=a,b,d,h:b=b*,h<minh1*,h2*,a>0,d>0.

To determine the direction of the Hopf bifurcation, we calculate the first Lyapunov number l1 at the equilibrium E5 = (x5, y5). Initially, we shift the equilibrium to the origin using the transformation (x̄,ȳ)=(xx5,yy5). Subsequently, we expand system Eq. 3 into a power series around the origin. Then, system Eq. 3 becomes

dx̄dt=α10x̄+α01ȳ+α20x̄2+α11x̄ȳ+α30x̄3+α21x̄2ȳ+P21x̄,ȳ,dȳdt=β10x̄+β01ȳ+β20x̄2+β11x̄ȳ+β02ȳ2+β30x̄3+β21x̄2ȳ+β12x̄ȳ2+Q21x̄,ȳ,

where P21(x̄,ȳ) and Q21(x̄,ȳ) are smooth functions of at least the fourth order with respect to (x̄,ȳ) and

α10=12x5x52d1+ax52,α01=x51+ax5,α11=12x51+ax52,α20=1+3ax58dx51+ax531,α30=5a2x5+4ax5+116dx5321+ax54,α21=1+3ax58x5321+ax53,β10=bd,β01=b,β20=bdx5,β11=2bx5,β02=bdx5,β30=bdx52,β21=2bx52,β12=bdx52.

In accordance with the formula for the first Lyapunov number l1 presented in [24] [p.353], we proceed with the computation

l1=3π2α01Δ32M,

where

M=α10α11β10α11+β02+α01β112+α20β11+α11β022β10β0222α01α202β20β02α0122α20β20+β11β20+α01β102α102β11β02α11α20α102+α01β103α01α30+2α10α21+β12β21β01,

and

Δ=α10β01α01β10=DetJE5>0,α01=x51+ax5<0.

Consequently, if l1 < 0 (which corresponds to M < 0), then E5 undergoes a supercritical Hopf bifurcation, leading to the emergence of a stable limit cycle in a small neighborhood of E5 as the parameters across the surface H1. Conversely, if l1 > 0 (or M > 0), a subcritical Hopf bifurcation occurs, resulting in an unstable limit cycle appearing in the vicinity of E5 as the parameters across the surface H1.

Given the complexity of l1, which does not readily reveal information about its sign, we turn to a numerical example for further clarification.

Fixing a = 0.4, d = 0.6, and h = 0.04, we obtain b* = 0.3960214438 and M = 0.537259605 and then l1 > 0, which implies that an unstable limit cycle is created around E5 = (0.1742665424, 00.2904442373). For b = 0.41 > b*, we obtain M = 0.652746120 and then l1 > 0, which implies that an unstable limit cycle is created around E5, where E5 is asymptotically stable (see Figure 5B). When b = 0.425, a collision occurs between the periodic orbit and saddle E4, resulting in the formation of a homoclinic orbit. Since M = 0.791862704, then l1 > 0, which means that periodic orbits remain unstable, as shown in Figure 5A.

Figure 5
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Figure 5. (A) Phase portrait of system (4) with a = 0.4, b = 0.425, d = 0.6, and h = 0.04. E1 is an unstable node, E2 is a saddle, E4 is a saddle, and E5 is a sink. It indicates that the periodic orbit undergoes a collision with the saddle E4. (B) Phase portrait of system (4) with a = 0.4, b = 0.41, d = 0.6, and h = 0.04. E1 is an unstable node, E2 is a saddle, E4 is a saddle, and E5 is a sink. An unstable limit cycle, depicted as a black curve, surrounds the equilibrium point E5.

4.3 Bogdanov–Takens bifurcation

As presented in Theorem 3.5, the positive equilibrium E3 is identified as a cusp of co-dimension 2. This classification holds under certain conditions where a10 + b01 = 0, h=h2*, f20 ≠ 0, and f11 ≠ 0. Consequently, system Eq. 3 may undergo a Bogdanov–Takens bifurcation in the immediate vicinity of E3.

Theorem 4.1. When h and d are selected as bifurcation parameters, system Eq. 3 is poised to experience a Bogdanov–Takens bifurcation in a neighborhood of E3 as (h, d) varies near (hBT, dBT) for a10 + b01 = 0, h=h2*, f20 ≠ 0, and f11 ≠ 0, where (hBT, dBT) represents the threshold value of bifurcation parameters such as Det(J(E3))(h,d)=(hBT,dBT)=0 and Tr(J(E3))(h,d)=(hBT,dBT)=0.

Proof. To obtain the expressions for the saddle-node, Hopf, and homoclinic bifurcation curves, we derive a normal form for the Bogdanov–Takens bifurcation. This derivation uses the techniques outlined by [11, 18, 25].

Let us examine a perturbation of the parameters h and d centered around their BT bifurcation values. We represent this perturbation as h = hBT + u and d = dBT + v, where u and v are small deviations from the critical values hBT and dBT, respectively. Consider

dxdt=x1xxy1+axhBTu,dydt=by1dBT+vyx.(9)

We begin by translating the equilibrium point E3 = (x3, y3) to the origin using the transformations X = xx3 and Y = yy3. Subsequently, we expand system Eq. 9 as a power series centered at the origin. Then, we have

Ẋ=m00+m10X+m01Y+m11XY+m20X2+P1X,Y,Ẏ=n00+n10X+n01Y+n11XY+n20X2+n02Y2+Q1X,Y,(10)

where P1(X, Y) and Q1(X, Y) are smooth functions of at least the third order with respect to (X, Y), whose coefficients depend smoothly on u and v, and where

m00=u,m10=12x3x32dBT1+ax32,m01=x31+ax3,n00=bvx3dBT2,m11=12x31+ax32,m20=1+3ax38dBTx31+ax331,n02=bdBT+vx3,n10=bdBT+vdBT2,n01=bdBT+2vdBT,n11=2bdBT+vx3dBT,n20=bdBT+vx3dBT2.

Let x = X and y = m00 + m10X + m01Y + m11XY + m20X2 + P1(X, Y), then system Eq. 10 can be written as

ẋ=y,ẏ=l00+l10x+l01y+l11xy+l20x2+l02y2+Q2x,y,(11)

where Q2(x, y) are smooth functions of at least the third order with respect to (x, y), whose coefficients vary smoothly on u and v, and

l00=m002n02m00m01n01+m012n00m01,l01=m10+n01m002n02+m11m01,l10=m01n10m00n11m10n01+m11n00+m00n022m10m01m00m11m012,l20=m11n10m10n11+m01n20+2m00m20+m102n02m01+m00m11n02m00m112m01m10m013,l11=2m20+n11+m00m11m11+2n02m012m10m11+2n02m01,l02=m11+n02m01.

By introducing a new variable τ through the relation dt = (1 − l02x) and subsequently rewriting τ back as t, we can recast system Eq. 11 in a new form:

ẋ=y1l02x,ẏ=1l02xl00+l10x+l01y+l11xy+l20x2+l02y2+Q2x,y.(12)

Let X = x and Y = y(1 − l02x), then system Eq. 12 can be written as

Ẋ=Y,Ẏ=d00+d10X+d01Y+d11XY+d20X2+Q3X,Y,(13)

where Q3(X, Y) are smooth functions of at least the third order with respect to (X, Y), whose coefficients depend smoothly on u and v, and

d00=l00,d10=l102l00l02,d01=l01,d11=l11l01l02,d20=l202l10l02+l00l022.

Note that d20 is very complex, and we cannot determine the sign of d20 when u and v are small. Hence, we consider two cases: C-1: d20 > 0; C-2: d20 < 0.

C-1: If d20 > 0 for small values of u and v, we perform the following change of variables: x = X, y=Yd20, and τ=d20t. Additionally, we retain variable t to represent τ. With these transformations, system Eq. 13 is transformed into a new form

ẋ=y,ẏ=h00+h10x+h01y+h11xy+x2+Q4x,y,(14)

where Q4(x, y) are smooth of at least the third order with respect to (x, y), whose coefficients depend smoothly on u and v, and

h00=d00d20,h10=d10d20,h01=d01d20,h11=d11d20.

Let X=x+h102 and Y = y, then system Eq. 14 can be written as

Ẋ=Y,Ẏ=g00+g01Y+g11XY+X2+Q5X,Y,(15)

where Q5(X, Y) are smooth of at least the third order with respect to (X, Y), whose coefficients depend smoothly on u and v, and

g00=h0014h102,g01=h0112h10h11,g11=h11.

Suppose d11 ≠ 0, then g11 = h11 ≠ 0. Making the change of variables x=g112X, y=g113Y, and τ=1g11t, we then obtain from system Eq. 15 that

ẋ=y,ẏ=μ1+μ2y+x2+xy+Q6x,y,

where Q6(x, y) are smooth of at least the third order with respect to (x, y), whose coefficients depend smoothly on u and v, and

μ1=g00g114,μ2=g01g11.(16)

C-2: If d20 < 0 for small u and v, we perform the following change of variables: x′ = X, y=Yd20, and τ=d20t. Additionally, we retain variable t to represent τ′. With these transformations, system Eq. 12 is transformed into a new form:

ẋ=y,ẏ=h00+h10x+h01y+h11xy+x2+Q5x,y,ε,(17)

where Q5(x,y) are smooth of at least the third order with respect to (x′, y′), whose coefficients depend smoothly on u and v, and

h00=d00d20,h10=d10d20,h01=d01d20,h11=d11d20.

Let X=xh102 and Y′ = y′, then system Eq. 17 can be written as

Ẋ=Y,Ẏ=g00+g01Y+g11XY+X2+Q6X,Y,(18)

where Q6(X,Y) are smooth of at least the third order with respect to (X′, Y′), whose coefficients depend smoothly on u and v, and

g00=h00+14h102,g01=h01+12h10h11,g11=h11.

Suppose d11 ≠ 0, g11=h110. Making x=g112X, y=g113Y, and τ=1g11t, we obtain the versal unfolding of system Eq. 18:

ẋ=y,ẏ=μ1+μ2y+x2+xy+Q7x,y,

where Q7(x,y) are smooth of at least the third order with respect to (x′, y′), whose coefficients depend smoothly on u and v, and

μ1=g00g114,μ2=g01g11.(19)

To streamline the analysis, we retain the notation μ1 and μ2 for the transformed parameters μ1 and μ2, as defined in Equation Eq. 19. This approach reduces the number of cases we must consider. If the Jacobian determinant |(μ1,μ2)(u,v)|(u,v)=(0,0) is non-zero, then the parameter transformations described by Eqs 16 and 19 are homeomorphisms in a small neighborhood of the origin. Consequently, μ1 and μ2 can be treated as independent parameters.

Drawing upon the findings obtained by [24] and as supported by [5, 11, 18, 26], we establish that system Eq. 9 experiences a Bogdanov–Takens bifurcation when the parameters (u, v) are in a small neighborhood of the origin. The local representatisons of the bifurcation curves, derived from the analysis, are as follows (“+” for d20 > 0, “-” for d20 < 0):

(1) The saddle-node bifurcation curve SN = {(u, v): μ1 = 0, μ2 ≠ 0};

(2) The Hopf bifurcation curve H={(u,v):μ2=±μ1,μ1<0};

(3) The homoclinic bifurcation curve HL={(u,v):μ2=±57μ1,μ1<0}.

Subsequently, we numerically illustrate the locations of the bifurcation curves and the dynamics of the system at the Bogdanov–Takens bifurcation point. This is achieved by selecting specific values for the dimensionless parameters. We choose a = 0.4 and dBT = 0.6, then hBT = 0.04485055333 and b = 0.5193087015. Since d20 = 1729.213892u2 − 1.159964346–9.646351129v − 31.60626034u − 319.1508390uv and d11 = (22.77081918–346.0816837u)v2 + (19.64233118–642.5091021u)v − 284.7831954u − 2.673388394, then d20 < 0 and d11 ≠ 0 for u ∈ (−0.01, 0.01) and v ∈ (−0.1, 0.1), so we compute Eq. 19 and get |(μ1,μ2)(u,v)|(u,v)=(0,0)=14.32953396713920. Hence, the parameter transformation Eq. 19 is nonsingular. The local representations of the bifurcation curves up to second-order approximations are as follows:

(1) The saddle-node bifurcation curve SN=(u,v):μ20,1.86375448162305v+16.9957334575794u+4614.59435174402u21401.21892975004uv+98.3266830247282v2};

(2) The Hopf bifurcation curve H=(u,v):μ1<0,1.86375448162305v+16.9957334575794u+4784.69223204402u21460.51719203213uv+103.494713194792v2};

(3) The homoclinic bifurcation curve HL=(u,v):μ1<0,0.950895143738617v+8.67129258088447u+2524.48275351690u2774.205879496251uv+55.3347051835753v2}.

These bifurcation curves H, HL, and SN divide the small neighborhood of the origin in the parameter plane (u, v) into four regions. The bifurcation diagram of system Eq. 9 is given in Figure 6A, from which we obtain the following observations:

Figure 6
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Figure 6. (A) Bifurcation diagram of system (26). (B) No positive equilibrium when (u, v) = (−0.01, − 0.1) lies in region I, and system (26) has two boundary equilibria E1 and E2.

(a) When (u, v) = (0, 0), the unique positive equilibrium is a cusp of co-dimension 2.

(b) When the parameters are situated within region I, the system lacks a positive equilibrium, as shown in Figure 6B. This absence implies that the prey population is inclined toward extinction under nearly all initial conditions.

(c) When the parameters are positioned along the curve SN, the system exhibits a positive equilibrium that is characterized as a saddle node.

(d) In region II, system Eq. 9 possesses two positive equilibria. Specifically, E4 is identified as a saddle, while E5 acts as a source, as shown in Figure 7A.

(e) Upon crossing curve H and entering region III, the system undergoes a subcritical Hopf bifurcation, resulting in the emergence of an unstable limit cycle. This phenomenon is depicted in Figure 7B.

(f) When the parameters are selected along the curve HL, an unstable homoclinic cycle encircles a sink, while the other equilibrium remains a saddle. This configuration is illustrated in Figure 8A.

(g) In region IV, the system is characterized by the presence of a sink and a saddle, as depicted in Figure 8B.

Figure 7
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Figure 7. (A) E5 is a source and E4 is a saddle when (u, v) = (−0.01, − 0.09) lies in region II. (B) E5 is a sink and E4 is a saddle when (u, v) = (−0.01, − 0.087) lies in region III, and an unstable limit cycle encloses E5.

Figure 8
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Figure 8. (A) E5 is a sink and E4 is a saddle when (u, v) = (−0.01, − 0.0854) lies on curve HL and an unstable homoclinic orbit encloses E5. (B) E5 is a sink and E4 is a saddle when (u, v) = (−0.01, − 0.08) lies in region IV.

5 Conclusion

In this paper, we explore a Leslie-type predator–prey system incorporating prey harvesting. Initially, we examine system Eq. 2 without prey harvesting, establishing that it possesses a unique boundary equilibrium and a unique positive equilibrium. Theorem 2.2 elucidates the stability of both boundary equilibrium and positive equilibrium. Notably, the boundary equilibrium is consistently unstable, indicating that neither the prey nor the predator will ever become extinct without the influence of prey harvesting.

Furthermore, we study the dynamic behaviors of system Eq. 3 to analyze the effect of prey harvesting on the prey and predator. Hence, we first analyze the existence and stability of equilibria for system Eq. 3 in Section 3. As shown in Theorem 3.1, we identify the maximum sustainable yield as hMSY=14. Beyond this threshold (h>14), both the prey and predator species face extinction. Our investigation into the stability of the positive equilibria reveals that the coexistence of both species is possible if b>b1* and the harvesting rate h=h2* is between h1* and hMSY, or if bb* and h is less than the minimum of h1* and h2*. Otherwise, either only the prey survives or both species become extinct. This insight underscores the importance of selecting an appropriate harvesting rate, specifically one that is below a critical threshold and less than hMSY to ensure the coexistence of the predator and prey, thereby sustaining ecological balance.

In Section 4, we chose the constant harvesting rate h as one of the bifurcation parameters to perform the bifurcation analysis of system Eq. 3. We find that system Eq. 3 has complex dynamic behavior and undergoes Hopf bifurcation, Bogdanov–Takens bifurcation of co-dimension 2, and saddle-node bifurcation. Among them, the emergence of saddle-node bifurcation means that system Eq. 3 has bi-stable behavior, and the prey may face extinction or sustain, which depends on the harvesting rate. For the Hopf bifurcation, we calculate the first Lyapunov number to ascertain the direction of the Hopf bifurcation, which indicates whether a stable or unstable limit cycle emerges in the vicinity of the equilibrium E5. By selecting two parameters from system Eq. 3 as bifurcation parameters, we demonstrate that the system undergoes a Bogdanov–Takens bifurcation of co-dimension 2. This conclusion is drawn from our analysis of the universal unfolding near the cusp.

In conclusion, we constructed and provided a detailed dynamic analysis of a Leslie-type predator–prey system that incorporates prey harvesting. Our findings reveal that prey harvesting introduces complex dynamic behaviors into the system, potentially leading to a series of bifurcations. Furthermore, if the harvesting intensity exceeds a critical threshold, the prey may face extinction. These insights offer valuable contributions to the understanding of predator–prey systems and ecological balance. However, it is worth noting that this paper focuses primarily on qualitative analysis and lacks empirical data to support our theoretical findings. Despite this, significant algorithms have been developed to gather and analyze real-world data. We intend to leverage these algorithms to quantitatively assess the impact of harvesting using the methodologies introduced by [27, 28]. Additionally, this study does not consider the removal of both prey and predator species, and human activity can significantly impact ecosystems, as highlighted by [29]. Drawing inspiration from [3036], our model can be extended to eco-epidemic systems and reaction–diffusion systems. These areas represent promising directions for future research in this field.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material; further inquiries can be directed to the corresponding author.

Author contributions

YZ: data curation, methodology, writing–original draft, and writing–review and editing. JL: methodology, writing–original draft, and writing–review and editing.

Funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. The research was supported by the National Natural Science Foundation of China (No. 12201582), Research Project Supported by Shanxi Scholarship Council of China (2022-151), and the Fundamental Research Program of Shanxi Province under grant (No. 202203021212130).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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Keywords: saddle-node bifurcation, Hopf bifurcation, prey harvesting, Bogdanov–Takens bifurcation, predation

Citation: Zhang Y and Luo J (2024) Bifurcation analysis of a Leslie-type predator–prey system with prey harvesting and group defense. Front. Phys. 12:1392446. doi: 10.3389/fphy.2024.1392446

Received: 27 February 2024; Accepted: 19 April 2024;
Published: 19 June 2024.

Edited by:

Hui-Jia Li, Beijing University of Posts and Telecommunications (BUPT), China

Reviewed by:

Jun Hu, Rey Juan Carlos University, Spain
Kaifa Wang, Southwest University, China

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*Correspondence: Jianfeng Luo, amlhbmZlbmdsdW9AbnVjLmVkdS5jbg==

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