
Citation: Rudy R. Negenborn, Peter-Jules van Overloop, Tamás Keviczky, Bart De Schutter. Distributed model predictive control of irrigation canals[J]. Networks and Heterogeneous Media, 2009, 4(2): 359-380. doi: 10.3934/nhm.2009.4.359
[1] | Chunmei Zhang, Suli Liu, Jianhua Huang, Weiming Wang . Stability and Hopf bifurcation in an eco-epidemiological system with the cost of anti-predator behaviors. Mathematical Biosciences and Engineering, 2023, 20(5): 8146-8161. doi: 10.3934/mbe.2023354 |
[2] | Santanu Bhattacharya, Nandadulal Bairagi . Dynamic optimization of fishing tax and tourism fees for sustainable bioeconomic resource management. Mathematical Biosciences and Engineering, 2025, 22(7): 1751-1789. doi: 10.3934/mbe.2025064 |
[3] | Jinxing Zhao, Yuanfu Shao . Bifurcations of a prey-predator system with fear, refuge and additional food. Mathematical Biosciences and Engineering, 2023, 20(2): 3700-3720. doi: 10.3934/mbe.2023173 |
[4] | Xiaoying Wang, Xingfu Zou . Pattern formation of a predator-prey model with the cost of anti-predator behaviors. Mathematical Biosciences and Engineering, 2018, 15(3): 775-805. doi: 10.3934/mbe.2018035 |
[5] | Saheb Pal, Nikhil Pal, Sudip Samanta, Joydev Chattopadhyay . Fear effect in prey and hunting cooperation among predators in a Leslie-Gower model. Mathematical Biosciences and Engineering, 2019, 16(5): 5146-5179. doi: 10.3934/mbe.2019258 |
[6] | Yuanfu Shao . Bifurcations of a delayed predator-prey system with fear, refuge for prey and additional food for predator. Mathematical Biosciences and Engineering, 2023, 20(4): 7429-7452. doi: 10.3934/mbe.2023322 |
[7] | William Wolesensky, J. David Logan . An individual, stochastic model of growth incorporating state-dependent risk and random foraging and climate. Mathematical Biosciences and Engineering, 2007, 4(1): 67-84. doi: 10.3934/mbe.2007.4.67 |
[8] | Mengya Huang, Anji Yang, Sanling Yuan, Tonghua Zhang . Stochastic sensitivity analysis and feedback control of noise-induced transitions in a predator-prey model with anti-predator behavior. Mathematical Biosciences and Engineering, 2023, 20(2): 4219-4242. doi: 10.3934/mbe.2023197 |
[9] | Ceyu Lei, Xiaoling Han, Weiming Wang . Bifurcation analysis and chaos control of a discrete-time prey-predator model with fear factor. Mathematical Biosciences and Engineering, 2022, 19(7): 6659-6679. doi: 10.3934/mbe.2022313 |
[10] | Hua Guo, Yuan Tian, Kaibiao Sun, Xinyu Song . Dynamic analysis of two fishery capture models with a variable search rate and fuzzy biological parameters. Mathematical Biosciences and Engineering, 2023, 20(12): 21049-21074. doi: 10.3934/mbe.2023931 |
In nature, there are many predator-prey relationships among various organisms, and this is also the reason for the balance of nature. This relationship has gone through a long process of natural evolution. Predators and prey have formed various adaptations of predation and anti-predation in structure, physiology, habits and lifestyle, forming a certain balanced relationship. In 2012, Choh et al. [1] found a phenomenon in an experiment that there is a role reversal (anti-predator behavior) between predators and prey. When the prey species were threatened, in order to survive and reproduce, they will fight back, and even kill the predators' juveniles. In 2013, Hoover et al. [2] revealed that fathead minnows exhibit typical anti-predator behavior; as a response to the predator scent signatures and chemical alarm cues, they will go into shelters and decrease activity. In 2015, O'Connor et al. [3] revealed that stimulated by the predators, cichlid fish species spend less time exploring and more time searching for cover and congregating with other similar species to avoid being attacked by predators. In addition, researchers have revealed that in the presence of predation hazards, many species such as the three-spined stickleback [4], monkey goby [5], red tilefish [6] and other species will exhibit anti-predator behavior.
To characterize the anti-predator behavior of prey species and analyze its impact on the dynamics of the system, many scholars have introduced the anti-predator effect into the predator-prey model [7,8,9,10,11,12]; among others, Tang and Xiao [7] revealed that the predator will go extinct as a consequence of the anti-predator behavior, which means that anti-predator behavior can aid prey species in resisting predator aggressiveness. Sun et at. [8] introduced a kind of anti-predator behavior, which occurs only when the prey group size is larger than a threshold. Mortoja et al. [9] introduced anti-predator behavior into a stage-structure model, and, through numerical simulations, they found that the anti-predator factor may change the system's stability. Prasad [10] analyzed an additional food provided predator-prey system with anti-predator behaviour in prey. Sirisubtawee et al. [11] introduced anti-predator behavior into an impulsive Holling type IV predator-prey model, and discussed the complex dynamics such as the periodic solution of the impulsive model. Tian and Gao [12] presented a predator-prey model with an anti-predation effect and prey-dependent threshold control and analyzed the dynamics of the proposed model.
On the other hand, fishing activities are carried out for both commercial and livelihood needs. However, it is worth pointing out that overfishing will always lead to depletion of fishery resources. Therefore, rational management of fishery resources is necessary from the perspective of renewable resources protection, and appropriate fishing levels can not only protect fishery resources, but also maximize profits. Fishing activities can be carried out in different manners, which include continuous form [13,14,15], semi-continuous form [16], periodic form [17,18] and state-dependent form [19,20,21]. Fishing activity is a typical human activity and it is usually determined by the density of the fish population. State-dependent harvesting strategy takes the current state of the species into consideration and avoid the adverse impacts on the sustainability of the species. There are many cases of human intervention in real world problems, which often occur at state-dependent times or involve state-dependent thresholds. For such situations, state-dependent strategies are usually used to model this phenomena or problems, and the corresponding system can be described by impulsive semi-dynamical systems (ISDSs) [22,23,24,25]. In the past two decades, many scholars have applied the theory and method of impulsive semi-dynamic system into different subjects and scientific problems, such as pest control [26,27,28,29,30], disease control [31,32], process of sugar manufacturing [33], prey-predator system [34,35,36,37,38], competitive system [39] and other subjects [40,41]. Predator-prey systems based on state feedback control had received much attentions, the corresponding models can be divided into predator-dependent [19,20], prey-dependent [42,43,44,45], ratio-dependent [46,47] and prey-predator hybrid-dependent [21,48,49]. In natural systems, predators and prey are mixed, so it is impossible to determine the exact number of the two species, but their proportions are usually kept constant. Based on this consideration, a weight capture strategy was introduced into a fishery model [21], where fishing activity is permitted when the weighted sum of both species populations reaches a threshold. In the current work, we present a predator-prey model with anti-predator behavior and analyze how anti-predator behavior affects system dynamics. Then, following application of the weight capture strategy to the system, we analyze the complex dynamics induced by a discontinuous weighted fishing strategy. In addition, in order to obtain the optimal fishing strategy that maximizes economic profits, we discuss the problem of fishing process optimization.
The article structure is as follows. In Section 2, we propose a predator-prey model for fisheries with anti-predator behavior and construct a capture model based on weighted fishing strategies, followed by presenting some basic knowledge. In the next section, we first investigate the effects of anti-predator behavior on system dynamics, and then discuss the complex dynamics of the system induced by a weighted fishing strategy. In addition, in order to maximize the economic profit, we carried out the study of the optimization of the fishing process. In Section 4, we discuss the numerical simulations performed to verify the theoretical results obtained in the previous section. In the last section, we present a summary and discussion.
Let x denote the prey density and y denote the predator density. Then the classical predator-prey model can be expressed as follows:
{dxdt=B(x)−yD(x),dydt=μyD(x)−sy, | (2.1) |
where, B(x) describes the prey growth rate, D(x) represents the functional response, s represents the predator mortality rate and μ denotes the conversion rate from prey to predator. In this study, the logistic type growth rate and Holling-II type functional response are considered, i.e., B(x)=rx(1−x/K) and D(x)=bx/(1+h1x).
When the prey species shows anti-predator behavior, let p characterize the anti-predator rate of the prey; the term −pxy is added to the change rate of predators. Then, Model (2.1) takes the form
{dxdt=rx(1−xK)−bxy1+h1x:=xP(x,y),dydt=μbxy1+hx−sy−pxy:=yQ(x), | (2.2) |
where r describes the intrinsic growth rate, K represents the environmental capacity, b denotes the predation rate, h1 is the saturation constant, h=h1+bh2 and h2 describes the conversion saturation constant. Considering the biological significance of the model, the study is regionally limited in Ω0={(x,y)|0≤x≤K,y≥0}.
For both commercial and livelihood needs, fishing activities are carried out when the fish populations satisfy certain conditions. Let w denote the proportion of prey species, (1−w) be the proportion of a predator population, H denote the threshold of the weighted sum of both species populations, E represent the capture strength and qi (i=1,2) denotes the capture rate. Besides, in order to prevent the extinction of predators caused by anti-predator behavior, a quantity of predator pups, denoted by τ, is released into the system. Based on the above capture strategies, the predator-prey model guided by the weighted fishing strategy is as follows:
{dxdt=rx(1−xK)−bxy1+h1xdydt=μbxy1+hx−sy−pxy}wx+(1−w)y≠H,Δx=−q1ExΔy=−q2Ey+τ}wx+(1−w)y=H | (2.3) |
where τ satisfies that τ<min{τ1,τ2}, and
τ1≜q2HE1−w,τ2≜q1HE1−w⋅1−q2E1−q1E. |
The research objective of this paper is to analyze how anti-predator behavior affects the dynamics of System (2.2), and also to discuss the complex dynamics of the Model (2.3) induced by a weighted fishing strategy. Besides, to obtain an optimal capture strategy that maximizes the economic profit, we discuss the problem of fishing process optimization.
We present some basic concepts and results of an ISDS for convenience, and the readers are referred to the literature [21,23,25,29,30,45].
Let us consider a planar impulsive model with following threshold
{dxdt=f1(x,y)dydt=f2(x,y)}χ(x,y)≠0,Δx=I1(x,y)Δy=I2(x,y)}χ(x,y)=0, | (2.4) |
where fi, Ii and χ are differentiable with respect to x and y. Let Ω represent the domain of solutions and π=(π1,π2): Ω×R→Ω characterize the solution map of the corresponding continuous system; define M≜{(x,y)∈Ω|χ(x,y)=0} and I=(I1,I2): M→N=I(M). Then we call the system constituted by (2.4) as an ISDS, which is denoted by (Ω,π;I,M). For any point S0∈N, the solution of (Ω,π;I,M) from S0 is denoted by z(t)=(x(t),y(t))′, i.e. z(0)=z0≜S0. The orbit is denoted by γS0(z)≜{z(t)|t≥0,z(0)=S0}. If γS0(z)∩M≠∅, the trajectory z(t) will reach the pulse set M many times due to the pulse action; the set of the time is denoted by Σ≜{tk|k=1,2,⋯}, i.e. z−k=z(tk)∈M and zk=I(z−k)∈N.
Definition 2.1 (Periodic solution [21,23,29,30,45]) The solution ˜z(t) with ˜z0∈N is said to be periodic if there exists n⩾1 satisfying ˜zn=˜z0. Denote m≜min{k|1≤k≤n,˜zk=˜z0}; then, ˜z(t) is called an order-m periodic solution with period T=tm.
Definition 2.2 (Oorbitally asymptotically stable [21,23,29,30,45]). For the periodic solution ˜z(t), if for an arbitrary ϵ>0, there is a neighborhood Uδ of ˜z, for any z∈Uδ, there exists a re-parameterized function ˆt(t) and |z(t)−˜z(ˆt(t))|<ϵ for all t≥t0; then, γ(˜z) is called orbitally asymptotically stable.
Definition 2.3 (Successor function [23,29,30]). Let us assume that M and N in (R2+,π,R+;M,I) are two disjoint lines. Denote N∩x-axis={O′}. For a given Q1∈N, denote γQ1(z)∩M={Q3}, γQ1(z)∩N={Q2} and Q4=I(Q3), as illustrated in Figure 1. Then the type-I successor function fIsor is defined by fIsor(Q2)=d(Q4,O′)−d(Q2,O′), and the type-II successor function fIIsor is defined by fIIsor(Q1)=d(Q4,O′)−d(Q1,O′).
Lemma 2.1 (Stability criterion [21,23,29,30,45]). The order-m periodic solution z(t)=(ξ(t),η(t))′ with the period T is said to be orbitally asymptotically stable if |μm|<1 holds, where
μm=n∏j=1Δjexp(∫T0[∂f1∂x+∂f2∂y](ξ(t),η(t))dt), |
with
Δj=f+1(∂I2∂y∂χ∂x−∂I2∂x∂χ∂y+∂χ∂x)+f+2(∂I1∂x∂χ∂y−∂I1∂y∂χ∂x+∂χ∂y)f1∂χ∂x+f2∂χ∂y, |
f+1=f1(ξ(τ+j),η(τ+j)), f+2=f2(ξ(τ+j),η(τ+j)) and f1, f2, ∂I1∂x, ∂I1∂y, ∂I2∂x, ∂I2∂y, ∂χ∂x and ∂χ∂y are calculated at (ξ(τj),η(τj)).
This section focuses on analyzing the dynamics of the free system (2.2) and the capture system (2.3), respectively. Since, in the case of μb⩽sh, there is dy/dt<0, i.e., the predator species will eventually become extinct. Therefore, from the perspective of ecological diversity, it is assumed that μb>sh.
For System (2.2), we mainly discuss the existence and stability of equilibria. For convenience, denote
F(x)≜r(1+h1x)(K−x)bK,p1≜ ub+sh−2√μbsh,m≜p+sh−μb, |
xp1≜{s/(μb−sh),p=0−m−√m2−4phs2ph,0<p<p1μb−p1−sh2p1h,p=p1,xp2≜{K,p=0−m+√m2−4phs2ph,0<p<p1K,p=p1 |
and ypi=F(xpi), i=1,2.
Define
g(p)=(2hh1−1)p−sh+μb−3√(p+sh−μb)2−4ph. |
Let ¯p∈(0,p1) satisfy g(¯p)=0. Since the dynamic behavior of System (2.2) are related to the parameters p and K, we divide the analysis into the following three cases:
(A1): 0≤p≤p1,xp1<K≤xp2;
(A2): 0<p<p1,K>xp2;
(A3): p>p1.
Further, (A1) is divided into five subcases:
(A1-1): 0≤p≤¯p, xp1<K≤2xp1+1/h1;
(A1-2): 0≤p≤¯p, 2xp1+1/h1<K≤xp2;
(A1-3): ¯p<p<p1, xp1<K≤xp2;
(A1-4): p=p1, xp1<K≤xp2
and (A2) is divided into three subcases:
(A2-1): ¯p<p<p1, xp2<K<2xp1+1/h1;
(A2-2): 0≤p<p1, K>K_≜max{2xp1+1/h1,xp2}.
In System (2.2), EO(0,0) and EK(K,0) always exist.
Theorem 3.1. In System (2.2), if Case (A1) holds, there exists a unique positive equilibrium E1; if Case (A2) holds, there exists two positive equilibria E1 and E2; for Case (A3), the positive equilibrium does not exist.
Proof of Theorem 3.1. Define Q0(x)=(1+hx)Q(x). Then, System (2.2) has a positive equilibrium if and only if the equation Q0(x)=0 has a positive root less than K. Since Q0(x)=0 does not have a positive root when p>p1, the positive equilibrium does not exist for Case (A3). While, for 0≤p≤p1, we have the following cases:
Case I: p=0. Then Q0(x)=0 has a unique positive root x=x01. Let y01=F(x01). Then E1(x01,y01) is a positive equilibrium if K>x01;
Case II: 0<p<p1. In this case, Q0(x)=0 has two positive roots x=xp1 and x=xp2. Let ypi=F(xpi),i=1,2. When xp1<K⩽xp2, E1(xp1,yp1) is a unique positive equilibrium. When K>xp2, E1(xp1,yp1) and E2(xp2,yp2) are two positive equilibria.
Case III: p=p1. In this case, Q0(x)=0 has two identical positive roots xE1=xp11. Let yp11=F(xp11). If K>xp11, then E1(xE1,yE1) is a unique positive equilibrium.
For any equilibrium ¯E(¯x,¯y), the Jacobian matrix is
J¯E=(P(¯x,¯y)+¯xPx(¯x,¯y)¯xPy(¯x,¯y)¯yQ′(¯x)Q(¯x)) |
The corresponding characteristic equation is
|λ¯E−J¯E|=λ2−p¯Eλ+q¯E=0, |
where
p¯E≜P(¯x,¯y)+¯xPx(¯x,¯y)+Q(¯x),q¯E≜P(¯x,¯y)Q(¯x)+¯xPx(¯x,¯y)Q(¯x)−¯x¯yPy(¯x,¯y)Q′(¯x). |
Theorem 3.2. EO(0,0) is a saddle point and unstable. EK(K,0) is a saddle point for Cases (A1-1)–(A1-3), and it is locally asymptotically stable for Cases (A1-4), (A2) and (A3). E1(xp1,yp1) is locally asymptotically stable for Cases (A1-1), (A1-3) and (A2-1), and unstable for Cases (A1-2), (A1-4) and (A2-2). E2 is a saddle point and unstable for Case (A2).
Proof of Theorem 3.2. Since qEO=−rs<0, EO is a saddle point. Given that qEK=−rQ(K), and for Cases (A1-1)–(A1-3), Q(K)>0; then, EK is a saddle point. For Case (A1-4), (A2) and (A3), Q(K)<0 and pEK=Q(K)−r<0; then, EK is locally asymptotically stable. When K=xp2, there is Q(K)=0; in this case, EK is a saddle-node.
For ¯E(¯x,¯y), we have
p¯E=−2rh1¯xk(1+h1¯x)[¯x−h1K−12h1],q¯E=b¯x2¯yQ′0(¯x)(1+h1¯x)(1+h¯x). |
For Cases (A1-1), (A1-3) and (A2-1), there exist qE1>0 and pE1<0 due to Q′0(xp1)>0 and K<2xp1+1/h1, which implies that E1(xp1,yp1) is locally asymptotically stable; for Cases (A1-2) and (A2-2), there is pE1>0; then, E1(xp1,yp1) is unstable. For Case (A1-2), there is ˙y≤0 and ˙y=0 if and only if x=xp1, so E1 is unstable. For Case (A1-2), a limit cycle ΓLC exists around E1. Since Q′0(xp2)<0 for Case (A2), i.e., qE2<0, E2(xp2,yp2) is a saddle point and unstable.
For System (2.3), there are
M={(x,y)|wx+(1−w)y=H},N={(x,y)|w1−q1Ex+1−w1−q2E(y−τ)=H}, |
and we denote kM≜−w/(1−w) and KN≜kM(1−q2E)/(1−q1E).
In this case, the system (2.2) has a subsystem (3.1) since y≡0 if y0=0
{dxdt=rx(1−xK),x≠xH,Δx=−q1Ex,x=xH, | (3.1) |
where w>0 and xH≜Hw−1.
Denote ¯ξ0=(1−q1E)xH and
T≜1rln(K−(1−q1E)xH(1−q1E)(K−xH)); | (3.2) |
then, a periodic solution exists in the subsystem (3.1):
¯ξ(t)=K(1−q1E)xHexp(r(t−(n−1)T)(K−(1−q1E)xH)+(1−q1E)xHexp(r(t−(n−1)T))),(n−1)T≤t≤nT. |
Define
R0≜(1−q2E)(1−q1E)sr(1−(h−1)Kq1ExH((1+h)K−(1−q1E)hxH)(K−xH))μbKr(1−h)(K−xHK−(1−q1E)xH)s+Kpr. |
Theorem 3.3. For the case w>0 and τ=0, if H<wK, there exists a periodic solution z=(¯ξ(t),0) in System (2.3), and it is orbitally asymptotically stable when R0<1.
Proof of Theorem 3.3. The proof can be seen as Theorem 2 in [21,45]; therefore, it is omitted here.
The intersection point of N with the x-axis is denoted as G(xG,yG). For 0<σ<τ, select a point Q∈N∩U(G,σ), where the trajectory z(t) with z(0)=Q intersects M at Q−, and denote Q+ as the phase point of Q− after the pulse.
The trajectory of System (2.2) tangent to N is denoted by ˆz(t), and the tangent point is denoted by A(xA,yA), i.e. dˆy/dˆx|A=kN. If γA(ˆz)∩M≠∅, let A− be the first intersection point, and A+ be the phase point of A− after the pulse. If γA(ˆz)∩M=∅ or γA′(ˆz)∩M={A−} for some A′(≠A)∈N, then let ˜z(t) be the trajectory tangent to M, and the tangent point is denoted by F, i.e. d˜y/d˜x∣F=kM. Moreover, let R1(xR1,yR1)∈N and R2(xR2,yR2)∈N with yR2<yR1 such that γRi(ˆz)∩M={F} (i=1,2). For Case (A1-2), if ΓLC∩M≠∅, then denote ΓLC∩M={M1,M2} with yM2<yM1. Similarly, if ΓLC∩N≠∅, then denote ΓLC∩N={N1,N2} with yN2<yN1.
Define Hi≜wxpi+(1−w)ypi (i=1,2) and
¯HpK≜{max{H|{π(A,t)|t≥0}∩M≠∅},for Cases(A1-1),(A1-3),max{H|ΓLC∩M≠∅},for Case(A1-2),wK,for Cases(A1-4),(A3). | (3.3) |
For Cases (A1) and (A3), we have
Theorem 3.4. For System (2.3), there exists an order-1 periodic solution for w>0 and H≤¯HpK in any case of (A1-1), (A1-3), (A1-4) and (A3). Moreover, for the case (A1-1) (or (A1-3)) and H>¯HpK, an order-1 periodic solution exists if xR2≤(1−q1E)xF. For the case (A1-2), an order-1 periodic solution exists for w>0 and H≤H1; while, for H1<H≤¯HpK, an order-1 periodic solution exists if xN2≤(1−q1E)xM2.
Proof of Theorem 3.4. In any case of (A1-1) or (A1-3) or (A1-4) or (A3), for w>0 and H≤¯HpK, any trajectory starting from N will intersect M, as illustrated in Figure 1. For the point A, if yA+=yA, then the orbit γA(z) forms an order-1 periodic solution. Otherwise,
i) In the case of yA+<yA, we have fIsor(A)=dA+G−dAG<0. Since fIsor(Q)=dQ+G−dQG>0, then ∃S∈¯AQ such that fIsor (S)=0, which means that the orbit γS(z) forms an order-1 periodic solution, as illustrated in Figure 2 (a);
ii) In the case of yA+>yA, we have fIsor(A)=dA+G−dAG>0. The orbit γA+(z) intersects M at A+−, and then it is pulsed to the point A++. Since yA−>yA+− and yA+>yA++, we have fIIsor(A+)=dA++G−dA+G<0. Next, according to the continuity of the solution, for ϵ=dAA+/2, we can select a point H∈N∩U(A,ϵ), and there is dH−A−<ϵ. Then, by the impulse effects, there is dH+A+≤max{1−q1E,1−q2E}ϵ<ϵ. Thus
fIIsor(H)=dH+G−dHG=dA+G−dH+A+−dAG−dAH.=dA+A−(dH+A++dAH)>0. |
The continuity of fIIsor implies that there exists S∈¯HA+ such that fIIsor(S)=0, as illustrated in Figure 2(b).
Moreover, for Case (A1-1) (or (A1-3)) and H>¯Hpw, if xR2≤(1−q2E)xF, then fIsor(R2)=dF+G−dR2G≤0. Similar to Case I), there exists an order-1 periodic solution in system (2.3). While, for (A1-2), we can adopt a proof similar to (A1-1); hence, it is omitted.
For Case (A2), two positive equilibria E1 and E2 exist simultaneously in System (2.2), where E2 is a saddle point, EK is locally asymptotically stable. Define
w∗i≜ypiK−xpi+ypi,i=1,2. |
For Case (A2-1), E1 is locally asymptotically stable. For Case (A2-2), E1 is unstable. Moreover, there exists ¯K>K_ and System (2.2) has a limit cycle ΓLC for K_<K<¯K. In this case, let ¯H≜max{H|ΓLC∩M≠∅}. For H1<H≤¯H, denote ΓLC∩M={D1,D2} with yD1≤yD2. Similarly, if ΓLC∩N≠∅, denote ΓLC∩N={B1,B2} with yB1≤yB2. For K≥¯K, EK is globally asymptotically stable.
Since E2 is a saddle point, let Γsm and Γusm respectively represent the stable and unstable manifolds that pass through E2 below the isoline ˙x=0. For H1<H≤H2, denote Γsm∩M={D}. If Γsm∩N≠∅, then denote B as the intersection point with a smaller y label. Otherwise, let B be a point on N with yB=(1−q2E)yD+τ. For H2<H≤wK, denote Γusm∩M={D}, and Γsm∩N={B}.
Theorem 3.5. For Case (A2), there exists an order-1 periodic solution in System (2.3) if one of the conditions holds: 1) 0<w≤w∗1 and H≤wK; 2) w∗1<w≤1 and H≤H1; 3) w∗1<w≤w∗2, H1<H≤wK and yB1≥(1−q2E)yD1+τ; 4) w∗2<w≤1, H2<H≤wK and yB≥(1−q2E)yD+τ.
Proof of Theorem 3.5. It can be easily verified that for any case of 1) 0<w≤w∗ and H≤wK or 2) w∗<w≤1 and H≤H1, any trajectory starting from N will intersect M; then, using a proof similar to Theorem 3.4, we can prove that there exists an order-1 periodic solution. While, for 3), w∗1<w≤w∗2 and H1<H≤H2, if yB1≥(1−q2E)yD1+τ, any trajectory starting from ¯B2G⊂N will intersects M; similarly, we can prove that there exists an order-1 periodic solution. Case 4) is similar to Case 3) and thereby omitted.
Let ˜z=(˜ξ(t),˜η(t)), 0≤t≤T be the order-1 P.S.. Denote ξ1=˜ξ(T),η1=˜η(T),ξ0=(1−q1E)ξ1, η0=(1−q2E)η1+τ, f01=f1(ξ0,η0),f11=f1(ξ1,η1),f02=f2(ξ0,η0) and f12=f2(ξ1,η1). Then, we have the following theorem.
Theorem 3.6. The order-1 periodic solution ˜z=(˜ξ(t),˜η(t)) is orbitally asymptotically stable if
∫T0(bh1˜ξ(t)˜η(t)(1+h1˜ξ(t))2−r˜ξ(t)K)dt<ln(|ξ0η0ξ1η1⋅wf11+(1−w)f12(1−q2E)wf01+(1−q1E)(1−w)f02|). | (3.4) |
Proof of Theorem 3.6. From Model (2.3), we have
f1(x,y)=rx(1−xK)−bxy1+h1x,f2(x,y)=μbxy1+hx−sy−pxy,χ(x,y)=wx+(1−w)y−H,I1(x,y)=−q1Ex,I2(x,y)=−q2Ey+τ. |
Then we have
∂f1∂x=r−2rxK−by(1+h1x)2,∂f2∂y=μbx1+hx−s−px,∂I1∂x=−q1E,∂I1∂y=0,∂I2∂x=0,∂I2∂y=−q2E,∂χ∂x=w,∂χ∂y=1−w. |
In addition,
Δ1=f+1(∂I2∂y∂χ∂x−∂I2∂x∂χ∂y+∂χ∂x)+f+2(∂I1∂x∂χ∂y−∂I1∂y∂χ∂x+∂χ∂y)f1∂χ∂x+f2∂χ∂y=(1−q2E)wf01+(1−w)(1−q1E)f02wf11+(1−w)f12, |
exp(∫T0(∂f1∂x+∂f2∂y)(˜ξ(t),˜η(t))dt)=ξ1η1ξ0η0exp∫T0(bh1˜ξ˜η(1+bh˜ξ)2−r˜ξK)dt. |
Thus,
μ1=Δ1exp(∫T0(∂f1∂x+∂f2∂y)(˜ξ(t),˜η(t))dt)=Δ1ξ1η1ξ0η0exp∫T0(bh1˜ξ˜η(1+bh˜ξ)2−r˜ξK)dt. |
Therefore, |μ1|<1 if and only if (3.4) holds; then, by Lemma 2.1, the order-1 periodic solution ˜z=(˜ξ(t),˜η(t)) is orbitally asymptotically stable.
Theorem 3.7. For the case (A1-1) (or (A1-3)) and H≤¯HpK, the order-1 periodic solution z=(˜ξ(t),˜η(t)) is orbitally asymptotically stable and globally attractive if yA+<yA.
Proof of Theorem 3.7. According to Theorems 4 and 5, when H≤¯HpK, there exists an order-1 P.S. in system (2.3). If yA+<yA, then L∈¯AQ, which means that for any S∈N, fIsor(S)<0 with yS>yL, fIsor(S)>0 with yS<yL and fIsor(S)=0 if and only if S=L. Thus, for any S+0∈¯AL⊂N, there exists a sequence {S+k}(k=0,1,2,⋯) satisfying yS+k+1=yS+k+fIsor(S+k). If S+0∈¯AL, {S+k} is monotonically decreasing. Moreover, yL is the lower limit. If S+0∈¯LQ, {S+k} is monotonically increasing, and yL is the upper limit. Thus yS+k→yS′(k→∞). Therefore,
fIsor(S′)=fIsor(limk→∞S+k)=limk→∞fIsor(S+k)=limk→∞(yS+k+1−yS+k)=0. |
Moreover fIsor(S)=0; then, we have S′=S, and the orbit from any point S+0⊂N will approach z=(˜ξ(t),˜η(t)), which means that z=(˜ξ(t),˜η(t)) is globally attractive.
Next, we discuss the order-2 periodic solution. For a given point S(xS,yS) on N with 0≤yS≤¯y≜(1−q2E)H/(1−w)+τ, when yS≤yA, there is ψN(yS)=(1−q2E)π(S,TS)+τ. While for yS>yA, there exists a unique S′∈N with yS′∈(0,yA) and ^Tz such that yS′=π(S,^TS). Then ψN(yS)=(1−q2E)π(S,TS′)+τ. For the above summary, there is
ψN(yS)={(1−q2E)π(S,TS)+τ,yS≤yA(1−q2E)π(S,TS′)+τ,yS>yA | (3.5) |
Property 3.1. For Case (A1) and H≤¯HpK, the Poincaré map ψN defined by (3.5) has the following characteristics: 1) ψN is continuous on [0,¯y]. Moreover, ψN increases and then decreases, and it reaches a maximum at y=yA; 2) ψN is continuously differentiable on [yA,¯y].
For Case (A1) and H≤HpK, if ψN(yA)<yA, the order-1 periodic solution of System (2.3) is orbitally asymptotically stable and globally attractive (Theorem 3.7); in this case, there does not exist an order-n (n≥2) periodic solution. For the case ψN(yA)>yA, there exists a unique yL2∈[yA,ψN(yA)] such that ψN(yL2)=yL2. Let yL1∈[0,yA] such that ψN(yL1)=yL2. Then ψ2N(yL1)=ψN(yL2)=yL2. Meanwhile, let yN1∈[0,yA] and yN2∈[yL2,¯y] such that ψN(yN1)=ψN(yN2)=yA.
Theorem 3.8. For w>0, H≤¯HpK and ψN(yA)>yA, if i) ψ2N(yA)<yA or ii) ψ2N(yA)>yA and μ1>1 holds, then there exists an order-2 periodic solution in System (2.3).
Proof of Theorem 3.8. Because ψN(yN1)=ψN(yN2)=yA, obviously, ψ2N(y1)=ψ2N(y2)=ψN(yA). Then, ψ2N is increasing on [0,yN1] and [yA,yN2] and ψ2N is decreasing on [yN1,yA] and [yN2,¯y]. Since ψ2N(yN1)=ψN(yA)>yA>yN1, there is ψ2N(yN1)>yN1.
i) If ψ2N(yA)<yA, then there is ψN(yA)>yN2. As ψN(yA)=ψ2N(yN2), there is ψ2N(yN2)>yN2, which also implies that ψ2N(ψN(yA))<ψN(yA). Thus there exist yM1∈[yN1,yA] and yM2∈[yN2,ψN(yA)] such that ψ2N(yM1)=yM1,ψ2N(yM2)=yM2. And there is ψN(yM2)=yM1,ψN(yM1)=yM2.
ii) If ψ2N(yA)>yA, there is ψN(yA)<yN2, i.e. ψ2N(yN2)<yN2. For any y∈[yA,ψN(yA)], we have yA<ψN(y)<ψN(yA). Next, it discusses the property of ψN on [yA,ψN(yA)]. Let y0=yA; then, y1=ψN(y0)=ψN(yA)>y0,y2=ψN(y1)=ψ2N(y0)>y0 and y3=ψN(y2)<ψN(y0)=y1. A sequence {yn} is obtained under ψN, where y0<y2<y4<⋯<yL2<⋯<y5<y3<y1. Denote yM1=limn→∞y2n and yM1=limn→∞y2n+1. It is obvious that yM1≤yL2≤yM2. Since μ1>1, yM1<yL2<yM2. Besides ψN(yM2)=yM1andψN(yM1)=yM2, so , i.e., the order-2 periodic solution is orbitally asymptotically stable.
In order to realize the sustainability of fishery resources and maximize economic benefits, it is necessary to consider the problem of harvest optimization. In Model (2.3), let , where , and the weight and harvest density are the decision variables. Besides, we assume that and are also linearly dependent on the decision variables and , i.e.
(3.6) |
where and are, respectively, the lower and upper limits of the harvest level, and respectively represent the minimum and maximum harvest effort and and respectively represent the minimum and maximum quantities of released predator populations. Let be the unit sale revenue of prey species, represent that of predator species, denote the unit price of harvesting and be the feeding predator unit cost. In general, and are fixed, and varies with season and market demand; also, denote . Therefore, the total revenue can be expressed as . The objective is to find the maximum of , which can be described as follows:
(3.7) |
The optimal control level , can be obtained by solving the optimization model (3.7). Accordingly, it is possible to determine the release amount , the optimal capture effort , and the optimal capture period .
We will verify the main results through numerical simulations. For System (2.2), we set the model parameters as follows , , , , , . Then there is .
First, for K = 100, how the anti-predator rate affects the dynamics of the system (2.2) is presented in Figure 3. When , two positive equilibria exist in the system; when , a unique positive equilibrium exists; and, when , there is no positive equilibrium. It is clear that the anti-predator factor has a certain effect on the number of equilibria; with the increase of the anti-predator factor, the number of positive equilibria gradually decreases.
Next, for , how the environmental capacity affects the dynamics of the system (2.2) is shown in Figure 4. For , is locally asymptotically stable, and for , is unstable; and, a limit cycle exists surrounding ; while, for , is globally asymptotically stable.
Next, we will verify the main results by changing the capture level . The control parameters were set as , , , and .
Case I: Here we consider three subcases:
i) and . Then a unique positive equilibrium exists in System (2.2). Since , for , there exists an order-1 periodic solution; its period is about , as shown in Figure 5-4.
ii) and . Then at the positive equilibrium , there is . For , there exists an order-1 periodic solution; its period is about , as illustrated in Figure 5-5.
iii) and . Then at the equilibrium , there is . For , an order-1 periodic solution with the period exists, as depicted in Figure 5-6.
Case II: In this case, the order-1 periodic solution exists conditionally. For , and , since holds for a given , and (Figure 6-1), an order-1 periodic solution exists (Figure 6-4); its period is about . It should be pointed out that the inequality is dependent on the values of , and ; once the inequality is reversed, all trajectories will go forward to after several pulses. For , and , System (2.3) also has an order-1 periodic solution with the period (Figure 6-5) since holds (Figure 6-2). For , and , since holds for a given , and (Figure 6-3), an order-1 periodic solution exists (Figure 6-6); its period is about .
For Case , we assume that ; then, , and . Diagrams of the trajectory tendency of the System (2.3) for different values of and are illustrated in Figure 7.
For , is locally asymptotically stable. Since , and , for , the order-1 periodic solution exists unconditionally (Figure 7-1); for and , when holds, the existence of the order-1 periodic solution is guaranteed (Figure 7-4 and Figure 7-7). For , is unstable and a limit cycle exists. In this case, , and . Similarly, for , the order-1 periodic solution exists unconditionally (Figure 7-2)), while for and , when holds, the existence of the order-1 periodic solution is guaranteed (Figure 7-5 and Figure 7-8). For , is unstable and is globally asymptotically stable. In this case, , and . Similarly, for , the order-1 periodic solution exists unconditionally (Figure 7-3); while, for and , when holds, the existence of the order-1 periodic solution is guaranteed (Figure 7-6 and Figure 7-9).
For Case (), when , is unstable and a limit cycle exists. For and a smaller with , there exists an order-1 periodic solution (Theorem 3.5, Figure 7-5). Notice that is just a sufficient condition to ensure that there is a periodic solution. In fact, as long as , for example, , the order-1 periodic solution will exist (Figure 8-1) for , and . For a bigger , for example, and , there may also exist an order-1 periodic solution (Figure 8-2, 8-3), but existence is not guaranteed. From Figure 8-2, it is observed that even if an order-1 periodic solution exists, its shape has changed. Figure 8-3 presents an order-2 periodic solution. The existence of an order-2 periodic solution implies the existence of an order-1 periodic solution, but in this case, the order-1 periodic solution is unstable.
The dynamics of System (2.3) depends on the control parameters , and . Next, we consider another set of control parameters: , and . For and , there is ; then, is unstable, is unstable and a limit cycle exists. We have . Presentation of the order- periodic solution of System (2.3) for , , and different values of is shown in Figure 9. For , System (2.3) has an order-2 periodic solution, as depicted in Figure 9-1. In this case, the order-1 periodic solution exists but is unstable. For , there exists an order-3 periodic solution (Figure 9-2) and for , System (2.3) has an order-4 periodic solution (Figure 9-3). The existence of an order- periodic solution () would also lead System (2.3) to chaos [42,50].
Let , , , and , and the other model parameters are the same as in the above simulations. Here, we consider two scenarios: 1) without anti-predator behavior, i.e., ; 2) with anti-predator behavior, i.e., . Besides, it is assumed that , , , and . For and , the dependence of and on and are presented in Figure 10. When , the unit benefit achieves its maximum at and . When , achieves its maximum at and .
For , is locally asymptotically stable. It is assumed that . For , the dependence of and on and are presented in Figure 11. For , the unit benefit achieves its maximum at and . For , achieves its maximum at and .
This work presented a fishery predator-prey model with anti-predator behavior and analyzed the dynamics of the model in detail. Besides, it introduced a weighted fishing strategy into the system and established a fishery capture model (2.2). It analyzed the dynamics of the model and showed that the anti-predation intensity affects the number of equilibria, that is, with the increase of anti-predation intensity, the number of equilibria will decrease (Figure 3). Moreover, it showed that, for a fixed anti-predator factor, the carrying capacity has certain impact on the stability of the equilibria (Figure 4).
It also discussed the dynamic behavior of the capture model (2.3) according to different levels of anti-predation factors. The results showed that an order-1 periodic solution always exists when , no matter how strong the anti-predator factor (Figure 5 and Figure 7). For , there is a constraint that ensures the existence of an order-1 periodic solution (Figure 6 and Figure 7). Moreover, for and , System (2.3) presents an order- periodic solution () for certain values of (Figure 8 and Figure 9). However, it is difficult and challenging to prove the existence of an order- periodic solution , which will be our next study.
In the numerical optimization, it was shown that the benefits from fishing processes are dependent on the unit sales price of prey and predators, as well as on the harvest unit cost. For given values of and , the unit benefit may achieve the maximum at different pairs of for different values of (Figure 10 and Figure 11). This also indicates that we can determine the optimal capture strategy (, and ) based on the selling prices of predators and prey, and then carry out fishing activities.
The research was supported by the Fundamental Research Funds for the Central Universities (No. DUT21LAB125).
The data used to support the findings of this study are available from the corresponding author upon request.
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
1. | Yuan Tian, Huanmeng Li, Kaibiao Sun, Complex dynamics of a fishery model: Impact of the triple effects of fear, cooperative hunting and intermittent harvesting, 2024, 218, 03784754, 31, 10.1016/j.matcom.2023.11.024 | |
2. | Guo Hua, Tian Yuan, Sun Kaibiao, Song Xinyu, Study on dynamic behavior of two fishery harvesting models: effects of variable prey refuge and imprecise biological parameters, 2023, 69, 1598-5865, 4243, 10.1007/s12190-023-01925-0 | |
3. | Hua Guo, Yuan Tian, Kaibiao Sun, Xinyu Song, Dynamic analysis of two fishery capture models with a variable search rate and fuzzy biological parameters, 2023, 20, 1551-0018, 21049, 10.3934/mbe.2023931 | |
4. | Cheng Chu, Wenjun Liu, Guangying Lv, Ali Moussaoui, Pierre Auger, Optimal harvest for predator–prey fishery models with variable price and marine protected area, 2024, 134, 10075704, 107992, 10.1016/j.cnsns.2024.107992 | |
5. | Yuan Tian, Xinrui Yan, Kaibiao Sun, Dual effects of additional food supply and threshold control on the dynamics of a Leslie–Gower model with pest herd behavior, 2024, 185, 09600779, 115163, 10.1016/j.chaos.2024.115163 | |
6. | Xiaoyue Yuan, Wenjun Liu, Guangying Lv, Ali Moussaoui, Pierre Auger, Sustainable management of predatory fish affected by an Allee effect through marine protected areas and taxation, 2024, 373, 00255564, 109220, 10.1016/j.mbs.2024.109220 | |
7. | Yongfeng Li, Song Huang, Xinyu Song, Global dynamic analysis of a nonlinear state-dependent feedback control SIR model with saturation incidence, 2023, 138, 2190-5444, 10.1140/epjp/s13360-023-04277-7 | |
8. | Xiaoxiao Yan, Zhong Zhao, Yuanxian Hui, Jingen Yang, Dynamic analysis of a bacterial resistance model with impulsive state feedback control, 2023, 20, 1551-0018, 20422, 10.3934/mbe.2023903 | |
9. | Yuan Tian, Hua Guo, Kaibiao Sun, Complex dynamics of two prey–predator harvesting models with prey refuge and interval‐valued imprecise parameters, 2023, 46, 0170-4214, 14278, 10.1002/mma.9319 | |
10. | Chenxi Huang, Qianqian Zhang, Sanyi Tang, Non-smooth dynamics of a SIR model with nonlinear state-dependent impulsive control, 2023, 20, 1551-0018, 18861, 10.3934/mbe.2023835 | |
11. | Liping Wu, Zhongyi Xiang, Dynamic analysis of a predator-prey impulse model with action threshold depending on the density of the predator and its rate of change, 2024, 9, 2473-6988, 10659, 10.3934/math.2024520 | |
12. | Yuan Tian, Chunxue Li, Jing Liu, Non-smooth competitive systems and complex dynamics induced by linearly dependent feedback control, 2024, 51, 1751570X, 101442, 10.1016/j.nahs.2023.101442 | |
13. | Wenjie Qin, Zhengjun Dong, Lidong Huang, Impulsive Effects and Complexity Dynamics in the Anti-Predator Model with IPM Strategies, 2024, 12, 2227-7390, 1043, 10.3390/math12071043 | |
14. | Xinrui Yan, Yuan Tian, Kaibiao Sun, Effects of additional food availability and pulse control on the dynamics of a Holling-(+1) type pest-natural enemy model, 2023, 31, 2688-1594, 6454, 10.3934/era.2023327 | |
15. | Shuai Chen, Wenjie Qin, Antipredator behavior of a nonsmooth ecological model with a state threshold control strategy, 2024, 9, 2473-6988, 7426, 10.3934/math.2024360 | |
16. | Yuan Tian, Xinlu Tian, Xinrui Yan, Jie Zheng, Kaibiao Sun, Complex dynamics of non-smooth pest-natural enemy Gomportz models with a variable searching rate based on threshold control, 2025, 33, 2688-1594, 26, 10.3934/era.2025002 | |
17. | Yuan Tian, Jing Zhu, Jie Zheng, Kaibiao Sun, Modeling and analysis of a prey-predator system with prey habitat selection in an environment subject to stochastic disturbances, 2025, 33, 2688-1594, 744, 10.3934/era.2025034 | |
18. | Yuan Tian, Hua Guo, Wenyu Shen, Xinrui Yan, Jie Zheng, Kaibiao Sun, Dynamic analysis and validation of a prey-predator model based on fish harvesting and discontinuous prey refuge effect in uncertain environments, 2025, 33, 2688-1594, 973, 10.3934/era.2025044 | |
19. | Xinrui Yan, Yuan Tian, Kaibiao Sun, Hybrid Effects of Cooperative Hunting and Inner Fear on the Dynamics of a Fishery Model With Additional Food Supplement, 2025, 0170-4214, 10.1002/mma.10805 | |
20. | XINYU BO, GUANGYING LV, WENJUN LIU, ALI MOUSSAOUI, OPTIMAL HARVEST CONTROL OF PREDATOR–PREY SYSTEMS IN FISHERIES WITH STAGE STRUCTURE AND ADDITIONAL FOOD SUPPLY, 2025, 33, 0218-3390, 221, 10.1142/S0218339025500032 | |
21. | Xinrui Yan, Yuan Tian, Kaibiao Sun, Dynamic analysis of a delayed pest-natural enemy model: Triple effects of non-monotonic functional response, additional food supply and habitat complexity, 2025, 18, 1793-5245, 10.1142/S1793524524500621 |