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Dynamics of a delayed phytoplanktonzooplankton system with CrowleyMartin functional response
Advances in Difference Equations volumeÂ 2017, ArticleÂ number:Â 5 (2017)
Abstract
In this paper, a delayed phytoplanktonzooplankton system with CrowleyMartin functional response is investigated analytically. We study the permanence and analyze the stability of the both boundary and positive equilibrium points for the system with delay as well as the system without delay. The global asymptotic stability is discussed by constructing a suitable Lyapunov functional. Numerical analysis indicates that the delay does not change the stability of the positive equilibrium point. Furthermore, we also show that due to the increase of the delay there occurs a Hopf bifurcation of periodic solutions. It is found that population fluctuations will not appear under the condition of certain parameters. In addition, we determine the direction of the Hopf bifurcation and the stability of bifurcating periodic solutions by applying a normal form method and center manifold theory. Finally, some numerical simulations are carried out to support our theoretical analysis results.
1 Introduction
Plankton plays an important role in the ocean and the climate because of their participation in the global carbon cycle at the base of the food chain [1]. There are two forms of plankton, the plant forms of the plankton community are known as phytoplankton and the animals in the plankton community are known as zooplankton. Phytoplankton biomass has the characteristics of rapid proliferation, this change is called bloom [2]. Under some circumstances, however, phytoplankton bloom can appear and affect the ecological balance, and it even can endanger human life and health. Therefore, a better understanding of mechanisms that determine the plankton dynamics is of considerable interest [3].
In recent years, there were many experimental ecologists as well as mathematical ecologists who have paid more attention to the phenomena of phytoplankton blooms. And many scholars proposed different deterministic models to study the dynamical behavior of the plankton system and tried to explain the dynamic mechanism of phytoplankton in different ways [4â€“11]. Abbas et al. [12] considered the two species competitive delay plankton allelopathy stimulatory deterministic model and investigated the existence and uniqueness of the solution as well as the persistence and the stability properties of the model, which is very useful and meaningful for the study of plankton bloom. Chakraborty and Das [13] investigated some properties of a twozooplankton onephytoplankton system that exhibits a Holling type II functional response in the presence of toxicity, the results they obtained can provide great help for researching the dynamic complexity of plankton systems. Kartal et al. [14] proposed a phytoplanktonzooplankton system via a new approach by using a system of differential equations with piecewise constant arguments and studied the biological dynamics of the bloom in the plankton system. It is significant that they explained the plankton bloom depended on three different parameters, namely Î¸ (rate of toxin production per phytoplankton), Î² (zooplankton growth efficiency) and K (environmental carrying capacity of phytoplankton), which can effectively promote the research process of the plankton bloom. However, a clear understanding of the mechanisms that cause the plankton blooms is still lacking. Hence, by establishing a differential equation model to study the ecological problems and a suitable model to study the dynamic relationship between the phytoplankton and zooplankton is still very important. In the work of [15] and [16], Stomp et al. and Rhee et al. have indicated that there exist many factors affecting the dynamics of plankton.
The functional response is one of the factors affecting the dynamic properties of plankton. Sklaski and Gilliam [17] pointed out that predatordependent functional responses such as described by BeddingtonDeAngelis, CrowleyMartin, and HasselVarley can provide a better description of predator feeding over a range of predatorprey abundance settings. In the above three functional responses, the CrowleyMartin [18] functional response is predator dependent and the per capita feeding rate is given by
where Ï‰, \(k_{1}\), and \(k_{2}\) are positive parameters that describe the effects of the capture rate, handling time, and the magnitude of interference among predators, respectively, on the feeding rate. It is obvious that the following two cases are possible. (1)Â If \(k_{1}>0\) and \(k_{2}=0\), then the response reduces to a MichaelisMenten (or Holling type II) functional response [19]. (2)Â If \(k_{1}=0\) and \(k_{2}=0\), then the CrowleyMartin response reduces to a linear massaction (or Holling type I) functional response [20].
It is interesting to study the dynamic properties of plankton systems with different functional responses [21, 22]. To the best of our knowledge, few studies of phytoplanktonzooplankton systems have applied a CrowleyMartin functional response. Based on the above discussion and the previous work of [23], we consider the following system:
For this system, in order to investigate the dynamics of the phytoplankton and zooplankton, we present the following major assumptions:
 (I_{1}):

It is assumed that \(P(t)\) and \(Z(t)\) are the concentrations of phytoplankton and zooplankton populations, respectively.
 (I_{2}):

It is assumed that \(k(\mathit{ugl}^{1})\) is the carrying capacity, \(r(\mathit{day}^{1}) \) is the maximum growth rate, \(\mu(\mathit{day}^{1})\) is the zooplankton death rate and Î³ is the conversion efficiency [23].
 (I_{3}):

It is assumed that Ï‰ is the effects of the capture rate, \(k_{1}\) is the handing time and \(k_{2}\) is the magnitude of interference among predator (zooplankton) [18].
 (I_{4}):

From a biological point of view, all the parameters in (2) assume only positive values and will be considered as constants throughout our discussion.
Let \(\bar{Z}=Z\), \(\bar{P}=kP\), and \(\bar{t}=rt\). Dropping the bars for simplicity, then (2) leads to the following dimensionless equations:
With \(P(0)=P_{0}>0\) and \(Z(0)=Z_{0}>0\), where \(a=\frac{1}{k^{2}}\), \(b=\frac{\omega}{r}\), \(c=\frac {k_{1}}{k}\), \(d=k_{2}\), \(e=\frac{k_{1}k_{2}}{k}\), \(h=\frac{\mu}{r}\), \(g=\frac {\gamma\omega}{k}\).
On the other hand, it is well known that biological systems governed by delaydifferential equations exhibit richer dynamics than ordinary differential systems [24â€“29]. Many ordinary differential models of plankton ignore the zooplankton from birth to have the ability to hunt and breed, it takes some time. Hence, a time delay factor is taken into account in the ecosystem so it will be more realistic. That is to say, in order to better understand the mechanisms that determine the plankton, it is necessary to study the dynamic behaviors for a phytoplanktonzooplankton system with consider the effect of a time delay. In recent years, the impact of different delays (such as maturation and gestation etc.) on plankton ecosystems has been extensively studied [30â€“36]. In this work, we assume that reproduction in a zooplankton population after predating on phytoplankton is not instantaneous, but is arbitrated by some constant time lag Ï„ because of phytoplankton handling and digesting. Under the same basic assumptions as taken for system (3), the dimensionless form of the delayed phytoplanktonzooplankton system is
subject to the initial conditions \(P_{0}=\zeta_{1}(\theta )>0\), \(Z_{0}=\zeta_{2}(\theta)>0\), \(\theta\in[\tau,0]\), where \(\zeta _{i}\in C([\tau,0]\rightarrow R_{+})\) for \(i=1,2\) are given functions and Ï„ is a positive constant.
The main purpose of this paper is to study the dynamic behaviors of system (3) and (4), especially, how the time delay affects the plankton system. We shall also compare all possible dynamics between the nondelayed system (3) and its corresponding delayed system (4). The remainder of the paper is organized as follows. In SectionÂ 2, we consider results for the nondelayed system (3), and we discuss the properties of positivity and boundedness, conditions for the existence of a positive equilibrium as well as the condition for the persistence, and the stability of various equilibrium points. SectionÂ 3 presents analogous results for the delayed system (4) and considers the stability and direction of the Hopf bifurcation. In SectionÂ 4, we present some numerical results supporting our analytical findings. SectionÂ 5 discusses the results and draws some conclusions.
2 Nondelayed system
In this section, our analysis shows the positivity and boundedness of the solutions, dissipativity, the persistence, local and global stability of both zooplanktonfree equilibrium and positive equilibrium points for system (3).
2.1 Positivity and boundedness of solutions
Let \(R_{+}\) denote the set of all nonnegative real numbers and \(R_{+}^{n}=\{P \in R^{n}:P=(P_{1}\cdots P_{n})\}\), where \(\{P_{i}\in R_{+},\forall i=1,2,\ldots, n\}\). If we denote the function on the righthand side of (3), by \(F=(F_{1},F_{2})\), it is clear that \(F\in C^{1}(R_{+}^{2})\). Thus, \(F:R_{+}^{2}\rightarrow R^{2}\) is locally Lipschitz on \(R_{+}^{2}=((P,Z):P\geq0,Z\geq0)\). Hence, the fundamental theorem of the existence and uniqueness ensures the existence and uniqueness of a solution for (3) with the given initial conditions. The state space for the system is a nonnegative cone \(R_{+}^{2}=\{(P,Z):P\geq0,Z\geq0\}\).
Lemma 2.1
The positive quadrant \((\operatorname{Int}(R_{+}^{2}))\) is invariant for system (3).
Now we consider the conservation of overall energy or biomass flow, and we search for the existence of some region in the dynamical space within which system (3) is bounded.
Lemma 2.2
[37]
Consider \(s(t)\) as an absolutely continuous function satisfying the differential inequality
where \((u_{1},u_{2})\in R^{2}\), \(u_{1}\neq0\). Then for all \(t\geq \hat{T}\geq0\) we have
Theorem 2.3
All the solutions of (3) starting in \(R_{+}^{2}\) are confined to the region \(D=\{(P(t),Z(t))\in R_{+}^{2}:0\leq P(t)\leq\frac{1}{a},0\leq\psi(t) \leq\frac {(h+1)^{2}}{4ah}\}\) as \(t\rightarrow\infty\) for all positive initial values \((P(0),Z(0))\in R_{+}^{2}\), where
Proof
We define the function
Differentiating \(\psi(t)\) with respect to time t along the solution for system (2), we obtain
Thus, we have
Using LemmaÂ 2.2, we have \(\psi(t)\leq\frac{(h+1)^{2}}{4ah}\) as \(t\rightarrow+\infty\). Therefore, all the solutions for (3) are uniformly bounded with an ultimate bound.â€ƒâ–¡
2.2 Dissipativity and permanence
In this section, we analyze the dissipativity, persistence, and permanence behavior of system (3). To prove our results, we first present the following definitions.
Definition 2.4
[38]
System (3) is said to be weakly persistent if every solution \((P(t),Z(t))\) satisfies two conditions:

(1)
\(P(t)\geq0\), \(Z(t)\geq0\), \(\forall t\geq0\).

(2)
\(\limsup_{t\rightarrow+\infty}P(t)>0\), \(\limsup_{t\rightarrow +\infty}Z(t)>0 \).
System (3) is said to be strongly persistent if every solution \((P(t),Z(t))\) satisfies the following condition along with the first condition for the weak persistence: \(\liminf_{t\rightarrow+\infty}P(t)>0\), \(\liminf_{t\rightarrow+\infty}Z(t)>0\).
Definition 2.5
[38]
System (3) is said to be permanent if there exists positive constants m and M, with \(0< m< M \) such that
for all solutions \((P(t),Z(t))\) of system (3) with positive initial values. System (3) is said to be nonpermanent if there is a positive solution \((P(t),Z(t))\) of system (3) such that
Lemma 2.6
[39]
If \(P>0\), \(q>0 \) and \(\frac{du}{dt}\leq(\geq)\, u(t)(qpu(t))\), \(u(t_{0})>0 \), then we have \(\limsup_{t\rightarrow+\infty}u(t)\leq\frac{q}{p}\) (\(\liminf_{t\rightarrow+\infty}u(t)\geq\frac{q}{p}\)). As the dependent variables are positive, from the phytoplankton equation in system (3), we have
Using LemmaÂ 2.6,
Thus, for arbitrary \(\varepsilon_{1}>0\) there exists a positive real number \(T_{1}\) such that
It is easy to see that
Applying LemmaÂ 2.6, we have
For arbitrary \(\varepsilon_{2}>0\) there exists a positive real number \(T_{2}\) such that
From the zooplankton equation in system (3), we have
Applying LemmaÂ 2.6 yields
Similarly, we can obtain
The above results can be summarized in the following theorem.
Theorem 2.7
For system (3), if \(h<\frac {gm_{1}}{1+cm_{2}} \), then
Theorem 2.8
For system (3), if \(d>b\) and \(h< \frac{gm_{2}}{1+cm_{1}}\), then
Remark 2.9
Under DefinitionÂ 2.4, TheoremÂ 2.7 results, whereby system (3) is weakly persistent (dissipative), holding provided \(h<\frac{m_{1}g}{1+cm_{2}}\). TheoremÂ 2.8 along with DefinitionÂ 2.4 ensures that system (3) is strongly persistent provided the conditions \(d>b \) and \(h<\frac{gm_{2}}{1+cm_{1}}\) hold.
The conditions \(d>b \), \(h<\frac{gm_{1}}{1+cm_{2}}\), and \(h<\frac {gm_{2}}{1+cm_{1}}\) ensure that \(m_{2}>0\), \(Q_{1}>0\), and \(Q_{2}>0\), respectively. Since \(m_{1}>0\) and \(\frac{gm_{1}}{1+cm_{2}}>\frac {gm_{2}}{1+cm_{2}}\), when \(h< \frac{gm_{2}}{1+cm_{1}}\) holds, this ensures that \(Q_{1}>0\) and \(Q_{2}>0\). Thus, we arrive at the following result.
Theorem 2.10
System (3) is permanent if it satisfies any of the following two conditions: (H_{1})Â \(d>b\), (H_{2})Â \(h<\frac{gm_{2}}{1+cm_{1}}\).
2.3 Biomass equilibrium
We consider the following three equilibrium solutions of system (3):

(i)
The trivial equilibrium \(E^{0}=(0,0)\).

(ii)
The boundary equilibrium \(E^{1}=(\frac{1}{a},0)\).

(iii)
The coexistence equilibrium (interior equilibrium) \(E^{*}=(P^{*},Z^{*})\).
Equilibria \(E^{0}\) and \(E^{1}\) always exist, and the coexistence equilibrium \(E^{*}=(P^{*},Z^{*})\) is the point of intersection of zero growth rate isoclines for phytoplankton (i.e. when \(\frac {dP(t)}{dt}=0\)) and zooplankton (i.e. when \(\frac{dZ(t)}{dt}=0\)), given by
where \(Z=\frac{gP(1aP)}{bh}\), and P is the root of the following equation:
where
From LemmaÂ 2.2 of Song et al. [40], since \(A_{3}<0\), we see that equation (6) has at least one positive root. We only consider that equation (6) has one positive root denoted by \(P^{*}\). Furthermore, for this value of \(P^{*}\), the corresponding value of \(Z^{*}\) is given by \(Z^{*}=\frac{gP^{*}(1aP^{*})}{bh}\).
2.4 Dynamical behavior: stability analysis
In this section, we deal with the local stability, global stability, and bifurcation of systemÂ (3).
2.4.1 Behavior of system (3) around \(E^{0}=(0,0)\)
The variational matrix for system (3) at \(E_{0} \) takes the form
We observe that the Jacobian matrix of system (3) at \(E^{0}\) has eigenvalues 1 and âˆ’h. Therefore, system (3) is always unstable around \(E_{0} \), which is in fact a saddle point.
2.4.2 Behavior of system (3) around \(E^{1}=(\frac{1}{a},0)\)
The variational matrix for system (3) at \(E^{1}\) takes the form
The eigenvalues of the variational matrix \(J(E^{1})\) at the equilibrium solution \(E^{1}\) are 1 and \(\frac{g}{a+c}h \). Hence, for \(h>\frac{g}{a+c}\) system (3) is stable around \(E_{1}\), for which the PZ plane is at stable manifold. Conversely, for \(h<\frac{g}{a+c}\), system (3) is always unstable around \(E^{1}\), which is, in fact, a saddle point.
From the above analysis, we have the following result.
Theorem 2.11
For system (3):

(i)
\(E^{0}\) is a saddle point.

(ii)
\(E^{1}\) is a saddle point if \(h<\frac{g}{a+c}\), and it is a stable node if \(h>\frac{g}{a+c}\).
Theorem 2.12
The equilibrium solution \(E^{1}=(\frac{1}{a},0)\) is globally asymptotically stable if \(h\geq \frac{g}{a}\).
We prove the result for the delayed system. The proof for system (3) is similar.
2.4.3 Behavior of system (3) around \(E^{*}=(P^{*},Z^{*})\)
Let \(P(t)=P^{*}+x(t)\), \(Z(t)=Z^{*}+y(t) \). Then the linearized system for (3) around the positive equilibrium \(E^{*}=(P^{*},Z^{*})\) is
The variational matrix for linearization of system (3) around \(E^{*} \) after simplification using the equilibrium equations for system (3) is given by
where
The characteristic polynomial for \(J(E^{*})\) is \(\lambda ^{2}\operatorname{tr}(J(E^{*}))\lambda+\operatorname{det}(J(E^{*}))\), where tr denotes trace and det stands for determinant. Applying the RouthHurwitz criteria, the characteristic polynomial will have either negative real roots or a pair of complex conjugate root with negative real part if \(\operatorname{tr}(J(E^{*}))<0\) and \(\operatorname{det}(J(E^{*}))>0\). Since \(\operatorname{tr}(J(E^{*}))=J_{11}+J_{22}\) and \(\operatorname{det}(J(E^{*}))=J_{11}J_{22}J_{12}J_{21}\), we have \(\operatorname{tr}(J(E^{*}))<0\) and \(\operatorname{det}(J(E^{*}))>0 \) if \(J_{11}<0 \), in other words, system (3) is stable in a small neighborhood of the nontrivial equilibrium \(E^{*} \) if
that is, if
Furthermore, we have the equilibrium equation (see the phytoplankton equation for system (3))
Using (9), equation (8) takes the form
Solving (9) for \(Z^{*}\), we have
Using (11), then inequality (10) takes the form
From (11), we have \(b(1aP^{*})(d+eP^{*})>0 \) and \(P^{*}\leq\frac {1}{a} \). Thus, equation (12) must hold provided
After some simple algebraic manipulations, equation (13) gives
Hence, if \(b>d \) and \(ab>cbcd+e \), then (14) is satisfied. Thus, we have the following result.
Theorem 2.13
If \(b>d \) and \(ab>cbcd+e \) hold, then the positive equilibrium is locally asymptotically stable.
2.4.4 Global stability of the interior equilibrium \(E^{*}=(P^{*},Z^{*})\) of system (3)
Theorem 2.14
If (H_{1})(H_{2}) hold and \((1+eQ_{1})(1aP^{*})< a \), then the interior equilibrium solution \(E^{*}\) is globally asymptotically stable.
Proof
We prove TheoremÂ 2.14 by constructing a suitable Lyapunov functional. Consider the functional \(V(P,Z): R_{+}^{2}\rightarrow R \) such that
where \(V_{1}(P)=(PP^{*}P^{*}\ln(\frac{P}{P^{*}})) \), \(V_{2}(Z)=(ZZ^{*}Z^{*}\ln(\frac{Z}{Z^{*}}))\), and u is a positive constant to be defined below. We evaluate the time derivative of the positive definite scalar valued function (15) along the solutions for system (3):
We define \(N(P,Z)=(1+cP+dZ+ePZ)(1+cP^{*}+dZ^{*}+eP^{*}Z^{*}) \). Differentiating (15) and inserting values of \(\frac{dV_{1}}{dt}\) and \(\frac{dV_{2}}{dt}\), algebraic manipulation yields
Using Theorems 2.7 and 2.8 and choosing u such that \(u(g\, dZ^{*}+g)=b+P^{*}\), we have
The coefficient for \((ZZ^{*})^{2}\) in (16) is always negative under the hypotheses of TheoremÂ 2.14. After inserting value of \(N(P,Z)\), the coefficient for \((PP^{*})^{2}\) takes the following form:
We conclude that if the hypotheses of TheoremÂ 2.14 are satisfied, then \(\frac{dV}{dt}<0 \) along all the trajectories in \(R_{+}^{2} \) except \(E^{*}=(P^{*},Z^{*})\). Thus, the functional \(V(P,Z) \) satisfies all the properties of a Lyapunov functional. Therefore, \(E^{*}=(P^{*},Z^{*})\) is globally asymptotically stable under the conditions of TheoremÂ 2.14. This completes the proof.â€ƒâ–¡
3 Delayed system
In this section, we analytically prove positivity and boundedness of the solutions, the persistence, local and global stability, existence of the Hopf bifurcation by analyzing the associated characteristic transcendental equation for the model with a delay. Furthermore, we also discuss stability and direction of the Hopf bifurcation by means of the normal form method and center manifold theory.
3.1 Positivity and boundedness of system (4)
First we prove the positivity of system (4). We can write the phytoplankton equation in system (4) as
Integrating from 0 to t, we obtain the following result:
which implies that \(P(t)>0 \) for all t when \(P(0)>0 \).
Using the zooplankton equation in system (4), we can write
which implies that \(Z(t)>0 \) for all t when \(Z(0)>0 \). Hence the interior of the first quadrant is an invariant set for the delayed system (4).
Theorem 3.1
All solutions for system (4) starting in \(R_{+}^{2} \) are confined to the region \(D^{*}=\{ (P,Z)\in R_{+}^{2}: 0\leq\phi(t)\leq\frac{(h+1)^{2}}{4ah}\} \) as \(t\rightarrow+\infty\) for all positive initial values \((P_{0}(\theta ),Z_{0}(\theta))\in R_{+}^{2}\), where \(\phi(t)= P(t\tau)+\frac {b}{g}Z(t) \).
Proof
We define the function \(\phi(t)=P(t\tau)+\frac{b}{g}Z(t) \). Differentiating \(\phi(t) \) with respect to time t along the solution for system (4), we obtain
Thus, we have
Using LemmaÂ 2.2, we have \(\phi(t)\leq\frac{(h+1)^{2}}{4ah} \). Thus all the solutions for system (4) are uniformly bounded with an ultimate bound.â€ƒâ–¡
3.2 Permanence
Now we establish the persistence and permanence behavior of the delayed model using the positivity of the dependent variables.
In SectionÂ 2, we showed the following relations for the phytoplankton equation in systemÂ (4):
and
From the zooplankton equation in system (4), we have
Solving (17), we have
Because \(\frac{gm_{1}}{(d+em_{2})h}>\frac {gm_{1}hcm_{2}h}{(d+em_{2})h}\equiv Q_{1} \), we obtain \(\limsup_{t\rightarrow+\infty}Z(t)\leq Q_{1} \).
Similarly, we have
Solving (18), we have
The above results can be summarized as follows.
Theorem 3.2
Any positive solution \(\{ P(t),Z(t)\} \) of system (4) satisfies
when \(d>b \) and \(h<\frac{m_{2}g}{1+cm_{1}} \).
Using the definitions of limâ€‰sup and limâ€‰inf, we can claim that there exist four positive constants \(t_{i}\) (\(i=1,2,3,4\)) such that
If we define \(N^{*}=\min\{ m_{2}, Q_{2}\}\), \(L^{*}=\max\{ m_{1},Q_{1}\}\), and \(T^{*}=\max\{ t_{1},t_{2},t_{3},t_{4}\} \), then we have \(N^{*}<\{ P(t),Z(t)\}<L^{*}\) for \(t>T^{*}\), and we can state the permanence result for system (3).
Theorem 3.3
The delayed system (4) is permanent if \(d>b \) and \(h< \frac{gm_{2}}{1+cm_{1}} \).
3.3 Local stability and Hopfbifurcation analysis
In this section we discuss the local stability of the positive equilibrium \(E^{*} \) and the boundary equilibrium \(E^{1} \) for system (4) and establish the existence of the Hopf bifurcation at \(E^{*}\). We recall the following result, which provides the conditions for the absence of a delayinduced switch from stability to instability.
Theorem 3.4
[41]
The set of necessary and sufficient conditions for \(E^{*} \) to be asymptotically stable for all \(\tau\geq0 \) is as follows:

(i)
The real parts of all the roots of \(D(\lambda,0)=0 \) are negative.

(ii)
For any real Z and any \(\tau\geq0 \), \(D(iZ,0)\neq0 \), where \(i=\sqrt{1} \), and \(D(\lambda,\tau)\) denotes the characteristic equation associated with (4).
We can rewrite system (4) as \(\frac{dW(t)}{dt}=F(W(t),W(t\tau)) \), where \(W(t)=[P(t),Z(t)]^{T}\) and \(W(t\tau)=[P(t\tau),Z(t\tau )]^{T} \). Let \(P(t)=P^{*}+x(t)\), \(Z(t)=Z^{*}+y(t) \). Then, linearizing system (4) about the interior equilibrium \(E^{*}=(P^{*},Z^{*}) \), we have
where \(G=(\frac{\partial F}{\partial W(t)})_{W^{*}} \), \(H=(\frac {\partial F}{\partial W(t\tau)})_{W^{*}} \), \(W^{*}=(P^{*},Z^{*}) \), and \(\varphi(t)=(x(t),y(t)) \).
Thus, the variational matrix for system (4) at \(E^{*} \) is given by \(J(E^{*})=G+He^{\lambda\tau} \), where
with
The variational matrix of system (4) at \(E^{1} \) is given by
and its corresponding characteristic equation is
where \(\lambda=1 \) is a negative eigenvalue. Hence, we only need to concentrate on the equation
It is clear that when \(\tau=0 \) and \(h>\frac{g}{a+c} \), the equilibrium point \(E^{1} \) is locally asymptotically stable. Substituting \(\lambda=i\omega\) into equation (20) and equating the real and imaginary parts, we obtain
Solving the above two equations, we have
Equation (22) has a positive root \(\omega_{+} \) if \(\frac{g}{a+c}>h \). Thus, there is a positive constant Ï„Ì‚ such that, for \(\tau>\hat{\tau} \), \(E^{1} \) becomes unstable.
The characteristic equation for system (4) at the positive equilibrium \(E^{*}\) takes the form
Then we have the following transcendental equation:
which has been extensively studied [42, 43]. Here \(D(\lambda ,0)=\lambda^{2}+(hj_{11})\lambdahj_{11}j_{12}(j_{21}+\frac {g}{b}j_{11}\frac{g}{b}\lambda)\). Hence, the constant term in \(D(\lambda,0)=0 \) is negative if \(h+j_{12}\frac{g}{b}>j_{11} \) and \(j_{12}(j_{21}+\frac{g}{b}j_{11})+hj_{11}<0 \). Therefore, regardless of the sign for Î», \(D(\lambda,0)=0 \) always has a unique positive root. Consequently, TheoremÂ 3.4 fails to ensure the stability of system (4) with positive delay \(\tau>0 \). We now determine the conditions under which the system undergoes a Hopf bifurcation near the coexistence equilibrium \(E^{*} \) and the local stability of \(E^{*} \). We take the discrete time delay Ï„ as the bifurcation parameter. We know that the sign for the real parts of the solution for (23) characterize the stability behavior of \(E^{*} \). Therefore, putting \(\lambda=\mu+i\omega\) into (23) and separating the real and imaginary parts, we obtain the following system of equations:
The necessary condition for a change in stability of the interior equilibrium point \(E^{*} \) is that equation (23) should have purely imaginary roots, that is, stability switches for increasing Ï„ in \(I=[0,\tau^{*})\) may occur only with a pair of roots \(\lambda=\pm i\omega(\tau)\). Let \(\tau=\hat{\tau}\) be the particular magnitude of Ï„ for which \(\mu(\hat{\tau})=0 \) and \(\omega(\hat{\tau })=\hat{\omega} \). Hence, to obtain the stability criterion, substituting \(\tau=\hat{\tau}\), \(\mu=0 \), and \(\omega=\hat{\omega }\) in (19), we obtain
Solving (25) for \(\cos\hat{\omega}\hat{\tau}\) and \(\sin\hat {\omega}{\hat{\tau}}\), we obtain
By squaring and adding the above two equations, we obtain a third order algebraic equation in Ï‰Ì‚ of the form
where
Let Î¾ be a real positive root of the cubic equation
Letting \(v=a_{0}x+a_{1} \), then equation (28) can be rewritten as
where
From LemmaÂ 2.2 of Wang et al. [44] we know that: (s_{1})Â If \(e_{2}<0 \), equation (29) has one positive root. (s_{2})Â If \(e_{2}>0 \) and \(e_{1}<0 \), equation (29) has two positive roots when \(e_{2}^{2}+4e_{1}^{3}<0 \) and has a positive root of multiplicity two when \(e_{2}^{2}+4e_{1}^{2}=0 \). (s_{3})Â If \(e_{2}=0 \) and \(e_{1}<0 \), equation (29) has one positive root.
The required value of Ï‰Ì‚, for which equation (23) has a pair of purely imaginary roots is the positive root of (27). From (26), the critical magnitude of the delay parameter corresponding to Ï‰Ì‚ is given by
for \(n=0,1,2,\ldots \)â€‰. If \(E^{*} \) is locally asymptotically stable for \(\tau=0 \), then by Butlerâ€™s lemma (see AppendixÂ 2 in [45]), \(E^{*} \) remains stable for \(\tau<\hat {\tau} \). The transversality condition for the Hopf bifurcation at \(\tau=\hat{\tau} \) is \([\frac{d\mu}{d\tau}]_{\tau=\hat{\tau }}>0 \). Differentiating (24) with respect to Ï„ and setting \(\tau =\hat{\tau} \), \(\omega=\hat{\omega}\), and \(\mu=0 \), we obtain
where
Thus, we have
From (30) it is obvious that the transversality condition \([\frac {d\mu}{d\tau}]_{\tau=\hat{\tau}}>0 \) for the occurrence of the Hopf bifurcation at \(\tau=\hat{\tau} \) is well satisfied provided \(\beta_{2}\beta_{1}+\alpha_{2}\alpha_{1}>0 \). Summarizing, we have established the following result for switching the stability behavior of system (4) around \(E^{*} \).
Theorem 3.5

(i)
Let \(E^{*} \) be locally asymptotically stable for system (4) with \(\tau=0 \) and let \(hj_{11}j_{12}(j_{21}+\frac{g}{b}j_{11})<0 \). Then there exists \(\tau=\hat{\tau} \) such that \(E^{*} \) is locally asymptotically stable for \(\tau<\hat{\tau} \) and unstable for \(\tau>\hat{\tau} \), where \(\hat{\tau}>0 \) is the smallest value for which there is a solution to equation (23) for which the real part is zero. Furthermore, as Ï„ exceeds Ï„Ì‚, \(E^{*} \) bifurcates into periodic solutions, provided \(\beta_{2}\beta _{1}+\alpha_{2}\alpha_{1}>0 \).

(ii)
If \(h+j_{12}\frac{g}{b}>j_{11} \), \(j_{12}(j_{21}+\frac {g}{b}j_{11})+hj_{11}<0 \), and (s_{1}) or (s_{2}) or (s_{3}) hold, then \(E^{*} \) for system (4) is locally asymptotically stable for all \(\tau>0 \).
3.4 Global stability of system (4) around \(E^{1} \) and \(E^{*} \)
We discuss the global stability of \(E^{1} \) and \(E^{*} \). Let \((P(t),Z(t))\) be any positive solution for (4) and let \(E^{1}=(\frac {1}{a},0)=(\bar{P},0) \). We consider the function
The time derivative of (31) along the positive solution of system (4) is
We introduce a functional \(V_{2} \) for (32) such that
Calculating \(\frac{dV_{2}}{dt} \) along the solution for system (4), we have
If \(h>\frac{g}{a} \) or \(h=\frac{g}{a}\), then from (35) we have \(\frac{dV_{2}}{dt}<0\) except at \((P(t),Z(t))=(\bar{P},0)\) and also \(\frac{dV_{2}}{dt}=0\) if and only if \((P(t),Z(t))=(\bar{P},0)\) (see the equation of (34)). Hence LyapunovLasalleâ€™s invariance principle implies the global asymptotic stability of \(E^{1} \).
We summarize the result in the following theorem.
Theorem 3.6
The equilibrium solution \(E^{1}=(\frac{1}{a},0) \) for system (4) is globally asymptotically stable if \(h\geq\frac{g}{a} \).
Theorem 3.7
If (H_{1})(H_{2}), \(a>bZ^{*}(c+eQ_{1})\), and the conditions
hold, then system (4) has a globally asymptotically stable equilibrium \(E^{*}\).
Proof
Consider the set \(\eta=\{ (P,Z):m_{2}< P< m_{1},Q_{2}< Z< Q_{1}\} \). It is clear that Î· is a compact and bounded region in \(R_{+}^{2} \) and is at a positive distance from the coordinate axes. There exists T, such that, for \(t>T \), every solution for system (4) with \(\tau>0 \) enters and remains in region Î·.
Using the equations for system (3), we can express system (4) as
Motivated by (36), to study the global stability of the interior solution \(E^{*}(P^{*},Z^{*}) \), we introduce the functional \(V(t) \) such that
where \(u_{1} \) and \(u_{2} \) are positive constants defined below and \(R=\frac{u_{2}gm_{1}(1+cP^{*})}{2Q_{2}\varphi_{1}} \), with \(\varphi _{1}=\varphi(m_{1},Q_{1})\), \(\varphi_{2}=\varphi(m_{2},Q_{2})\), and \(\varphi(P,Z)=(1+cP^{*}+dZ^{*}+eP^{*}Z^{*})(1+cP+dZ+ePZ)\).
Differentiating \(V(t)\) along the solution for system (36) and using
we have
The righthand side of the above expression should be considered as a quadratic form in the variables \((PP^{*})\) and \((ZZ^{*})\), that is, negative definite if the matrix G is
We define \(W=\frac{g Q_{2}P^{*}(d+em_{2})}{Q_{1}\varphi_{1}}\frac {Q_{1}(1+g \, dZ^{*})}{2Q_{2}\varphi_{2}}\frac {gm_{1}(1+cP^{*})}{2Q_{2}\varphi_{2}} \) and \(K=\frac{\varphi _{2}gm_{1}(1+cP^{*})}{Q_{2}\varphi_{1}(abcZ^{*}b e Q_{1}Z^{*})} \). If we choose \(u_{1}=Ku_{2} \), then the matrix G is positive definite if \(a>bZ^{*}(c+eQ_{1})\), \(W>0 \), and \(4W\{ \frac{K(abcZ^{*}beQ_{1}Z^{*})}{\varphi_{2}}\frac {gm_{1}(1+cP^{*})}{2Q_{2}\varphi_{1}}\}\geq\frac {b(1+cP^{*})^{2}}{\varphi_{1}^{2}} \), that is, \(Q_{2}\varphi _{2}(b(1+cP^{*}))^{2}K^{2}4Q_{2}W\varphi _{1}^{2}(abcZ^{*}beQ_{1}Z^{*})K2W\varphi_{1}\varphi _{2}gm_{1}(1+cP^{*})\leq0 \). The result follows.â€ƒâ–¡
Remark 3.8
If \(h\geq gP^{*} \), the sufficient conditions for global asymptotic stability of the positive solution \(E^{*} \) for nondelayed system (3) imply that the interior equilibrium solution \(E^{*} \) for the delayed system is globally asymptotic stable if \(E^{*} \) for nondelayed system (3) is globally asymptotic stable and conditions (i) and (ii) of TheoremÂ 3.7 hold.
3.5 Stability and direction of Hopf bifurcation
Here we describe the process for computing the direction of the Hopf bifurcation and the stability of bifurcating periodic solutions using the normal form method and center manifold theory introduced by Hassard et al. [46]. Without loss of generality, we always assume that system (4) undergoes a Hopf bifurcation in the state \(E^{*} \) for one of the critical values \(\tau=\hat{\tau}_{j}=\hat {\tau} \), where \(j=1,2,3,\ldots\) and \(\pm i\omega\) are the only purely imaginary roots of the characteristic equation at \(E^{*} \).
Let \(\sigma=\tau\hat{\tau} \). Then \(\sigma=0 \) is a Hopfbifurcation value of system (4). Letting \(P=x+P^{*}\), \(Z=y+Z^{*}\), and \(t=t\tau\), system (4) is transformed into
where
We can write equation (37) as the following functional differential equation in \(C=C([1,0),R^{2}) \):
where \(x(t)=(x_{1}(t),x_{2}(t))^{T}\in R^{2}\), \(L_{\sigma }:C\rightarrow R\), and \(F:R\times C\rightarrow R \) are given by
and
for which \(\phi(\theta)=(\phi_{1}(\theta),\phi_{2}(\theta ))^{T}\in C \), \(B_{1} \), \(B_{2} \), and \(F(\sigma,x_{t})\) are defined in the form
By the Riesz representation theorem [47], there exists a function \(\eta(\theta,\sigma)\) of bounded variation for \(\theta \in[1,0] \) such that
In fact, we can choose
where Î´ is the Dirac delta function. For \(\phi\in ([1,0],R^{2})\), we define
and
Then system (38) is equivalent to
where \(x_{t}(\theta)=x(t+\theta)\) for \(\theta\in(1,0] \).
For \(\kappa\in C^{1}([0,1],(R^{2})^{*})\), we define
To construct the coordinates to describe \(C_{0}\) near 0, for \(\kappa \in[\tau,0] \), we define the bilinear inner product
where \(\eta(\theta)=\eta(\theta,0)\). Then \(\langle\kappa,A\phi \rangle=\langle A^{*}\kappa,\phi\rangle\) and hence \(A(0)\) and \(A^{*}\) are adjoint operators. From the discussion in the previous subsection and the foregoing assumption, we know that \(\pm\hat{\omega}\hat{\tau} \) are eigenvalues of \(A(0)\). Hence, they are also eigenvalues of \(A^{*}\). We first need to compute the eigenvectors of \(A(0)\) and \(A^{*}\) corresponding to \(i\hat{\omega}\hat{\tau}\) and \(i\hat{\omega}\hat{\tau} \).
We can see that
are the eigenvectors of \(A(0)\) and \(A^{*}\) corresponding to \(i\hat {\omega}\hat{\tau}\) and \(i\hat{\omega}\hat{\tau}\), where
such that \(\langle q^{*}(s),q(\theta)\rangle=1\) and \(\langle q^{*}(s),\bar{q}(\theta)\rangle=0 \).
Following the same algorithms and using a similar computation process to that of Tripathi et al. [38], we obtain the coefficients for the important parameters:
where
Consequently, \(g_{21}\) can be expressed explicitly. Thus, we can compute the following values:
According to Hassard et al. [46] and using the quantity analysis above, the Hopfbifurcation properties are determined using the following theorem.
Theorem 3.9
The Hopfbifurcation properties at the critical value \(\tau=\hat{\tau} \) are derived, as follows:

(i)
If \(\mu_{2}>0\) (<0), the Hopf bifurcation is supercritical (subcritical).

(ii)
If \(\beta_{2}<0\) (>0), the bifurcated periodic solutions are stable (unstable).

(iii)
If \(T_{2}>0\) (<0), period of the bifurcating periodic solution increases (decreases).
4 Numerical simulations
In the previous sections, a detailed theoretical analysis has been carried out and some interesting results of the research of system have been obtained. In order to prove the feasibility and effectiveness of the theoretical analysis results as well as to provide a more indepth understanding of the results of the analysis, in particular, the time delay influencing the complex dynamics of phytoplanktonzooplankton system, we perform some numerical simulations.
The numerical solutions are given considering the following parameter values: \(a=1\), \(b=5\), \(c=2\), \(d=6\), \(e=0.001\), \(h=0.3\), and \(g=5\). For this choice, it is easy to show that the parameters can satisfy the conditions of TheoremÂ 2.14 when \(\tau=0\). And thus the positive equilibrium point \(E^{*}=(0.3937050691, 0.7956712927 )\) has global attractivity, which implies that the phytoplankton and zooplankton populations may have lasting coexistence, as shown in FigureÂ 1. In addition, these parameters can also satisfy the conditions of TheoremÂ 3.7 when we take \(\tau=2.5 \), and the positive equilibrium point \(E^{*}=(0.3937050691, 0.7956712927 )\) and this also shows global attractivity in the phytoplanktonzooplankton system with a time delay (see FigureÂ 2). Furthermore, it is interesting to compare FigureÂ 1 and FigureÂ 2, especially in FigureÂ 1(c) and FigureÂ 2(c), where it can be seen that the phase diagram of FigureÂ 2 becomes finer, which indicates that the delay does not change the stability of the positive equilibrium point, but it can also accelerate the process of its stability. To further illustrate the point, we plot phase portraits with the same initial value, and when \(\tau=2.5\) and \(\tau=0\) in FigureÂ 3, and the time series diagram for six different values of delay: 0, 0.5, 2.5, 5, 7.5, and 12 in FigureÂ 4 are taken, this explicitly depicts that the time delay does not affect the stability of the positive equilibrium point.
Next, the direction of the Hopf bifurcation for the corresponding delayed system (4) is also investigated by a numerical simulation. We take \(a=1\), \(b=8\), \(c=3.09\), \(d=1.2\), \(e=0.0005\), \(h=1.1\), and \(g=8 \), then it is not difficult to obtain \(\hat{\omega}=0.5393409834 \), \(\beta_{1}\beta _{2}+\alpha_{2}\alpha_{1}>0 \), \(\hat{\tau}=0.4422694125 \). It is easy to verify that the positive equilibrium \(E^{*}=(0.2931263460, 0.1883666284) \) for system (4) is locally asymptotically stable when \(\tau<\hat{\tau} \), the case of \(\tau=0.110\) is illustrated in FigureÂ 5. More interesting, when Ï„ passes through the critical value Ï„Ì‚, the positive equilibrium \(E^{*}=(0.2931263460, 0.1883666284) \) for system (4) loses its stability and a Hopf bifurcation occurs. Moreover, there exists a positive period1 solution caused by the Hopf bifurcation, the case of \(\tau=0.59\) is shown in FigureÂ 6. The model simulation also shows that the delay can enhance the amplitude of the periodic solution when the periodic solutions exist, which means that the delay has a large effect on the dynamics of system (4), as proved in FigureÂ 7. In additional, from SectionÂ 3.5, we can easily obtain \(c_{1}(0)=837.7866+8777.8357i \), \(\mu _{2}=12147.066>0\), \(\beta_{2}=1675.5732<0\), and \(T_{2}=51246.7726<0\), which shows that the Hopf bifurcation is supercritical and the bifurcation periodic solutions are stable with decreasing period.
5 Discussion and conclusion
Over the two decades, a great deal of research has been devoted to the dynamics of the plankton ecosystem, however, a clear understanding of the mechanisms that cause the plankton blooms is still lacking and, therefore, it has been remained an interesting area of research for many ecologists and mathematical biologists [30]. In this paper, an attempt has been made to study the dynamic behaviors of a phytoplanktonzooplankton system with a CrowleyMartin functional response and its corresponding delayed version. In order to see how the length of gestation delay affects the dynamical behavior, we have first analyzed the system without delay and obtained the parameters conditions for the permanence (TheoremÂ 2.10). That is, if (H_{1}) and (H_{2}) hold, the phytoplankton and zooplankton populations of the system will have lasting coexistence. It is also derived that the system in the absence of delay remains locally asymptotically stable when \(b>d\) and \(ab>cbcd+e\) (TheoremÂ 2.13), which means that phytoplankton blooms will not occur. More interesting, it can be concluded that the positive interior equilibrium of the system without delay is globally asymptotically stable under the conditions of TheoremÂ 2.14 (see FigureÂ 1). From the biological point of view, it leads the phytoplankton and zooplankton populations to coexist.
Next we have presented analogous results for the delayed system and considered the stability and direction of the Hopf bifurcation. It is should be noted that the system in the presence of delay is also globally asymptotically stable if (H_{1})(H_{2}), \(a > bZ^{*}(c + eQ_{1})\), and (i)(ii) hold (see FigureÂ 2). In the work of [2, 12, 34, 35, 42, 48], one showed that the time delay can cause a stable equilibrium to become unstable and even a switching of stabilities in their system, in other words, a time delay which incorporates in a biological ecosystem can lead to the ecosystemâ€™s steady state switch from stable to unstable. In particular, in [34], the authors also investigated the dynamical behavior of a phytoplanktonzooplankton system with a gestation delay, they observed that the gestation delay has a destabilizing effect on the system dynamics. However, in the present paper, based on the comparative analysis of the global stability of the numerical simulation results, it was found that the delay (gestation) did not change the stability of the system (FigureÂ 1(a) and (b) and FigureÂ 2(a) and (b), FiguresÂ 3 and 4). In [4], where the global stability and the Hopf bifurcation in a zooplanktonphytoplankton system was studied, the obtained results also showed that the time delay did not change the stability of the system. Additionally, our results also indicated that the delay can accelerate the process of its stability (FiguresÂ 1(c) and 2(c)). Although the delay cannot change the stability of the system, it should be emphasized that the delays were bound to influence the process. These results may be very meaningful to study the dynamics of phytoplanktonzooplankton interaction and may have great importance for research on plankton bloom.
In addition, it has also been shown that the time delay can induce instability and oscillations via a Hopf bifurcation in the system in the case of the presence of delay, and thereafter, switching of stability occurs. In other words, the stability of system (4) can be changed by the delay. More specifically, we have established that when \(\tau<\hat{\tau}=0.4422694125\), the positive interior equilibrium \(E^{*} \) is stable under certain parametric restrictions mentioned in TheoremÂ 3.5. However, when the time delay Ï„ exceeds the threshold value \(\hat{\tau}=0.4422694125 \), the delayed phytoplanktonzooplankton system will undergo a Hopf bifurcation and exhibit a periodic orbit around the coexisting equilibrium point \(E^{*} \) (see FigureÂ 6). It should be noted that gestation delay can enhance the population fluctuations when the delay is long enough, however, our analytical results demonstrated that population fluctuations will not appear if \(h+j_{12}\frac{g}{b}>j_{11} \), \(j_{12}(j_{21}+\frac{g}{b}j_{11})+h j_{11}<0 \) and any of (s_{1}), (s_{2}), (s_{3}) hold (TheoremÂ 3.5). From the biological point of view, it implies the disappearance of bloom of plankton populations. Consequently, the gestation delay on CrowleyMartin functional response of the zooplankton can ensure some mechanism for controlling the plankton bloom. This may be helpful to study the problem of plankton bloom. Furthermore, by virtue of the normal form method and center manifold theory, we have derived that a Hopf bifurcation is supercritical (\(\mu_{2}>0\)) and the bifurcation periodic solutions are stable with decreasing period (\(\beta_{2}<0\) and \(T_{2}<0\)).
Finally, although the study of the problems of the limit in theory study, the data of numerical simulations are not based on real world survey, it can be seen that numerical simulation results support our analytical findings. Hence, our work may be helpful to field investigation and experimental research in the real situation, as well as may also be helpful for qualitative research into similar real systems in nature. Nevertheless, in the real world, the environment of the planktonic creature is random, we also believe that our theoretical results will be useful in the study of delayed CrowleyMartintype phytoplanktonzooplankton model systems in a stochastic environment, which we leave for future work.
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Acknowledgements
This work was supported by the National Natural Science Foundation of China (Grant Nos.Â 31370381 and 31570364).
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Liao, T., Yu, H. & Zhao, M. Dynamics of a delayed phytoplanktonzooplankton system with CrowleyMartin functional response. Adv Differ Equ 2017, 5 (2017). https://doi.org/10.1186/s1366201610554
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DOI: https://doi.org/10.1186/s1366201610554