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Hybrid control of Hopf bifurcation in a LotkaVolterra predatorprey model with two delays
Advances in Difference Equations volumeÂ 2017, ArticleÂ number:Â 387 (2017)
Abstract
In this paper, the Hopf bifurcation control for a LotkaVolterra predatorprey model with two delays is studied by using a hybrid control strategy. By analyzing the associated characteristic equation, its local stability and the existence of Hopf bifurcation with respect to both delays are established. In addition, the onset of an inherent bifurcation is delayed. Based on the normal form theory and the center manifold theorem, explicit formulas are derived to determine the direction of Hopf bifurcation and stability of the bifurcating periodic solution. Numerical simulation results confirm that the hybrid controller is efficient in controlling Hopf bifurcation.
1 Introduction
In species dynamics, there are two kinds of mathematical models: the continuous temporal models described by differential equations and the discrete temporal models described by difference equations. The complex dynamics of these systems had attracted intensive as well as research attention in theoretical and mathematical biology during the last few decades. Some of the key discrete temporal models [1â€“5] and continuous temporal models [6â€“12] are referenced.
It is well known that significant theoretical development has recently been reported in the bifurcation theory of discrete temporal dynamic systems. There have been great and interesting predatorprey systems with time delay. This factor has induced more complicated dynamic characteristics than that without time delay because the presence of time delay causes a stable equilibrium to become unstable and subsequently the species to fluctuate. In [1], Han and Liu studied a discrete temporal model of LotkaVolterra type with delay by a set of difference equations as follows:
where \(x_{k}\) is the density of the first population at the kth generation, \(y_{k}\) denotes the density of the second population at the kth generation, \(r_{i}\) is the growth rate of population i, \(a_{ij}\) (\(i,j = 1,2\)) stands for the intensity of intraspecific competition or interspecific action of species. They focus on the stability and bifurcation analysis and the direction analysis of the NeimarkSacker bifurcations. This kind of discrete temporal model usually describes certain insects whose populations have nonoverlapping generations or the number of populations is small in nature.
However, depending on the different species, some recent works showed that the continuous temporal models are more appropriate than the discrete temporal models when the populations have overlapping generations or the number of populations is big. In real situations, there are different time delays of species that affect the predatorprey systems. For instance, the species feedback time delay, the hunting delay, the gestation period of prey or predator, etc.
In this paper, we consider the following system with two delays described by differential equations with reference to Xu et al. [13]:
where \(x(t)\) and \(y(t)\) can be interpreted as the population densities of prey and predator at time t, \(r_{1} > 0\) represents an intrinsic growth rate of the prey and \(r_{2} > 0\) denotes the death rate of the predators; the parameters \(a_{ij}\) (\(i,j = 1,2\)) are all positive constants in which \(a_{11}\) and \(a_{22}\) represent the intraspecific competition rate of prey and predator, \(a_{12}\) is the capturing rate, \(a_{21} / a_{12}\) is the conversion rate of the predator, \(\tau_{1}\) is the time delay due to the gestation of prey and predator, \(\tau_{2}\) in the first equation of system (1.2) denotes the hunting delay of predator to prey and \(\tau _{2}\) in the second equation of system (1.2) is the feedback delay of the predator to the growth of the species itself.
The dynamical behavior of the predatorprey systems with time delay has been studied comprehensively [14â€“22]. In the real world, there is sometimes a need to control a population at a reasonable level because otherwise this population may cause decrease or even extinction of other populations. With respect to the control of a biological system, the focus at present is on the state feedback control [23, 24] by changing the structure of the biocenose and by increasing the feeding pressure of the prey. For example, in order to eliminate algal bloom, an effective way is to introduce suitable fish species (chub etc.) that usually feed on plankton such that algal bloom can be controlled.
Hybrid control methods have been widely used by researchers [25â€“35]. Liu and Chung [27] proposed a hybrid control strategy for bifurcation in a continuous nonlinear dynamics system without time delay. Cheng and Cao [28] considered Hopf bifurcation control for a complex network model with time delays, and they used a hybrid control strategy to control the model. Chen et al. [30] proposed a new hybrid control strategy for microgrids with masterslave structure. In gridconnected operational mode, the droop control strategy was adopted for the main converter, while in standalone operational mode the droop gain would decrease to zero,thus becoming a conventional control. Ayadathil and Venkatesh [32] presented a hybrid control strategy for a matrix converter fed wind energy conversion system. Alfi et al. [35] investigated a hybrid control strategy for synchronization of a class of nonlinear chaotic systems by incorporating sliding mode control and state feedback control techniques via fuzzy logic. However, the hybrid control of bifurcation for a predatorprey system has not been extensively investigated. In this paper, a new control strategy of a system described in Eq. (1.2) is established. In the past, we mainly considered the state feedback control. For example, in order to eliminate the algal bloom, an effective way is to introduce a state feedback variable in the equation (such as chub) to change the system equilibrium. In fact, intraspecific effect coefficients, the interaction coefficients and others (e.g. temperature, irradiance, etc.) are affected by many factors. Furthermore, the parameters can be changed to regulate the system.
Motivated by Xu et al. [13] and based on a hybrid control by combining the state feedback control and perturbation parameter, the designing of a controller is established in this work in an effort to delay the occurrence of Hopf bifurcations in system (1.2). Here, a controlled system as follows is considered:
where \(\alpha> 0\), \(\beta\in R\) is a control parameter. The parameters \(x(t)\), \(y(t)\), \(a_{11}\), \(a_{12}\), \(a_{21}\), \(a_{22}\), \(r_{1}\), \(r_{2}\), \(\tau_{1}\) and \(\tau_{2}\) are defined in system (1.2). \(\beta x(t  \tau_{1})\) and \(\beta y(t  \tau_{1})\) can affect the densities of prey and predator at time \(t  \tau_{1}\), respectively, \(\beta> 0\) denotes increase in the quantity, while \(\beta< 0\) otherwise.
The biological meaning of system (1.3) can be interpreted as follows. In the absence of predators, the prey species follows the logistic equation \(\dot{x}(t) = \alpha x(t)[r_{1}  a_{11}(x  \tau_{1})]\), while in the presence of predators, there is a hunting delay \(a_{12}y(t  \tau_{2})\), with a certain delay \(\tau_{2}\) called the hunting delay. In the absence of prey species, the predator species follows the equation \(\dot{y}(t) = \alpha y(t)[  r_{2}  a_{22}y(t  \tau_{1})] + \beta y(t  \tau_{1})\). The positive feedback \(a_{21}x(t  \tau_{2})\) has a positive delay \(\tau_{2}\) which is the delay in the predator maturation.
The remainder of this paper is organized as follows. In SectionÂ 2, the local stability and the existence of Hopf bifurcation at a positive equilibrium are discussed and the onset of an inherent bifurcation is delayed by analyzing the corresponding characteristic equations. The direction of Hopf bifurcation and the stability of bifurcating periodic solutions are derived in SectionÂ 3. In SectionÂ 4, numerical simulations are carried out to illustrate the validity of the main results. A brief conclusion is given in the last section.
2 Local stability and Hopf bifurcation of the controlled system
In this section, we shall investigate the stability of system (1.3) at the positive equilibrium and the existence of Hopf bifurcation by analyzing the corresponding linearized system.
System (1.3) has a unique positive equilibrium \(E^{ *} (x^{ *},y^{ *} )\), where
if the following condition

(H1)
\((\alpha r_{1} + \beta)a_{22}  (\alpha r_{2}  \beta)a_{11} > 0\)
holds.
Let \(\bar{x}(t) = x(t)  x^{ *} \), \(\bar{y}(t) = y(t)  y^{ *} \) and denote \(\bar{x}(t)\), \(\bar{y}(t)\) by \(x(t)\), \(y(t)\), respectively, then system (1.3) becomes
where
Then we obtain a linearized system of system (2.1) as follows:
The corresponding characteristic equation of system (2.2) is
To investigate the root distribution of the transcendental equation (2.3), the result of Ruan and Wei [36] is introduced here.
Lemma 2.1
For the transcendental equation
as \((\tau_{1},\tau_{2},\tau_{3}, \ldots,\tau_{m})\) vary, the sum of orders of the zeros of \(p(\lambda,e^{  \lambda\tau_{1}}, \ldots,e^{  \lambda \tau_{m}})\) in the open right half plane can change, and only a zero appears on or crosses the imaginary axis.
In the sequel, we consider the following three cases.
Case (a) \(\tau_{1} = \tau_{2} = 0\), the characteristic equation (2.3) becomes
According to the RouthHurwitz criteria, a set of necessary and sufficient conditions for all roots of Eq. (2.4) to have a negative real part are given in the following form:

(H2)
\(m_{1} + m_{2} + n_{1} + n_{3} < 0\).
Then the equilibrium point \(E^{ *} (x^{ *},y^{ *} )\) is locally asymptotically stable when condition (H2) is satisfied.
Case (b) \(\tau_{1} = 0\), \(\tau_{2} > 0\), Eq. (2.3) reduces to
where
For \(\omega> 0\), suppose iÏ‰ is a root of Eq. (2.5), it follows that
which leads to
It is easy to see that if the condition

(H3)
\((p^{2}  2r) > 0\), \(r^{2}  q^{2} > 0\),
holds, then Eq. (2.7) has no positive roots. Hence, all roots of Eq. (2.5) have negative real parts when \(\tau_{2} \in[0,\infty)\) under conditions (H2) and (H3). Further, if (H2) and

(H4)
\((p^{2}  2r) > 0\), \(r^{2}  q^{2} < 0\),
hold, then Eq. (2.7) has a unique positive root \(\omega_{0}^{2}\). Substituting \(\omega_{0}^{2}\) into Eq. (2.6), we obtain
According to the Hopf bifurcation theorem [37], we need to verify the transversality condition. Differentiating Eq. (2.5) with respect to \(\tau_{2}\) and noticing that Î» is a function of \(\tau_{2}\), we obtain
which leads to
Noting that
Hence, we have
According to the analysis above and Corollary 2.4 of [36], we have the following results.
Lemma 2.2
For \(\tau_{1} = 0\), assume that (H1) and (H2) are satisfied, then the following conclusions hold:

(i)
If (H3) holds, then the positive equilibrium \(E^{ *} (x^{ *},y^{ *} )\) of system (1.3) is asymptotically stable for all \(\tau_{2} \ge0\).

(ii)
If (H4) holds, then the positive equilibrium \(E^{ *} (x^{ *},y^{ *} )\) of system (1.3) is asymptotically stable for all \(\tau_{2} \in [0,\tau_{20})\) and unstable for \(\tau_{2} > \tau_{20}\). Furthermore, system (1.3) undergoes a Hopf bifurcation at the positive equilibrium \(E^{ *} (x^{ *},y^{ *} )\) when \(\tau_{2} = \tau_{20}\).
Case (c) \(\tau_{1} > 0\), \(\tau_{2} > 0\). We consider (2.3) with \(\tau_{2}\) in its stable interval, and \(\tau_{1}\) is regarded as a parameter. Without loss of generality, we consider system (1.3) under assumptions (H2) and (H4). Let iÏ‰ (\(\omega> 0\)) be the root of Eq. (2.3), then we obtain
Separating the real and imaginary parts, we have
where
which lead to
where
Since \(\sin\omega\tau_{1} = \pm\sqrt{1  \cos^{2}\omega\tau_{1}}\), we consider the following two cases:
(i) \(\sin\omega\tau_{1} = \sqrt{1  \cos^{2}\omega\tau_{1}}\), Eq. (2.11) becomes
It is easy to compute \(\cos\omega\tau_{1}\) by Eq. (2.12) noting that
Hence, we can determine
and Ï‰ is a root of \(f_{1}^{2}(\omega) + f_{2}^{2}(\omega) = 1\).
(ii) \(\sin\omega\tau_{1} =  \sqrt{1  \cos^{2}\omega\tau_{1}}\), Eq. (2.11) becomes
It is easy to compute \(\cos\omega\tau_{1}\) by Eq. (2.13), noting that
Hence, we can determine
and Ï‰ is a root of \(f_{1}^{*2}(\omega) + f_{2}^{*2}(\omega) = 1\).
Let
hence, for \(\tau_{2} \in[0,\tau_{2_{0}})\), Eq. (2.3) has a pair of purely imaginary roots \(\pm i\omega^{ *} \) when \(\tau_{1} = \tau_{1_{0}}\).
In the following, we assume that

(H5)
\([\frac{d(\operatorname{Re} \lambda)}{d\tau_{1}}]_{\lambda= i\omega^{ *}} \ne0\).
We have the following theorem.
Theorem 2.1
If conditions (H1), (H2), (H4) and (H5) hold and \(\tau_{2} \in[0,\tau_{2_{0}})\), then the positive equilibrium \(E^{ *} (x^{ *},y^{ *} )\) of system (1.3) is asymptotically stable for \(\tau _{1} \in [0,\tau_{1_{0}})\) and unstable when \(\tau_{1} > \tau_{1_{0}}\). Furthermore, system (1.3) undergoes Hopf bifurcation at \(\tau_{1} = \tau_{1_{0}}\).
3 Direction and stability of Hopf bifurcation of the controlled system
In the previous section, we have shown that the controlled system (1.3) undergoes Hopf bifurcation for different combinations of \(\tau_{1}\) and \(\tau_{2}\). In this section, we will investigate the direction of Hopf bifurcation and the stability of bifurcating periodic solutions of the controlled system (1.3). Throughout this section, we assume that system (1.3) undergoes a Hopf bifurcation for \(\tau _{2}^{*} \in (0,\tau_{2_{0}})\) and \(\tau_{1} = \tau_{1_{0}}\). The theoretical approach we apply is based on the normal form theory and center manifold theory [37].
Without loss of generality, we assume that \(\tau_{2}^{*} < \tau_{1_{0}}\), where \(\tau_{2}^{*} \in(0,\tau_{2_{0}})\). For convenience, let \(\bar{u}_{i}(t) = u_{i}(\tau t)\) (\(i = 1,2\)) and \(\tau_{1} = \tau_{1_{0}} + \mu\), where \(\tau_{1_{0}}\) is defined by Eq. (2.14) and \(\mu \in R\), then system (1.3) can be written as a functional differential equation (FDE) in \(C = C([  1,0],R^{2})\):
where \(u(t) = (x(t),y(t))^{T} \in C\), \(u_{t}(\theta) = u(t + \theta ) = (x(t + \theta),y(t + \theta))^{T} \in C\), and \(L_{\mu}: C \to R\), \(F:R \times C \to R\) are given by
and
with
and
By the Riesz representation theorem, there exists a \(2\times2\) matrix function \(\eta(\theta,\mu)\), \(\theta\in[  1,0]\), whose elements are of bounded variation, such that
In fact, we can choose
For \(\varphi\in C([  1,0],R^{2})\), define
and
Then Eq. (3.1) can be transformed into the following operator equation:
where \(u_{t} = u(t + \theta) = (u_{1}(t + \theta),u_{2}(t + \theta))\), \(\theta\in[  1,0]\).
For \(\phi\in C([  1,0],(R^{2})^{ *} )\), where \((R^{2})^{ *} \) is the 2dimensional space of row vectors, we further define the adjoint operator \(A^{ *} \) of \(A(0)\):
For \(\varphi\in C([  1,0],R^{2})\) and \(\phi\in C([  1,0],(R^{2})^{ *} )\), define the bilinear form
where \(\eta(\theta) = \eta(\theta,0)\), \(A = A(0)\) and \(A^{ *} \) are adjoint operators. From SectionÂ 2, we know that \(\pm i\omega^{ *} \tau_{1_{0}}\) are eigenvalues of \(A(0)\), and they are also the eigenvalues of \(A^{ *} \) corresponding to \(i\omega^{ *} \tau_{1_{0}}\) and \( i\omega^{ *} \tau_{1_{0}}\). Further, we suppose \(q(\theta) = (1,\alpha )^{T}e^{i\omega^{ *} \tau_{1_{0}}\theta} \) is the eigenvector of \(A(0)\) corresponding to \(i\omega^{ *} \tau_{1_{0}}\) and \(q^{ *} (s) = M(1,\alpha^{ *} )e^{i\omega^{ *} \tau_{1_{0}}s}\) is the eigenvector of \(A^{ *} \) corresponding to \( i\omega^{ *} \tau_{1_{0}}\), where \(M = 1/D\).
By the direct calculation, we obtain
Then we have \(\langle q^{ *} (s),q(\theta) \rangle= 1\), \(\langle q^{ *} (s),\bar{q}(\theta) \rangle= 0\).
Next, we use the same notations as those in Hassard [37] and firstly compute the coordinates to describe the center manifold \(C_{0}\) at \(\mu= 0\). Let \(u_{t}\) be the solution of Eq. (3.1) when \(\mu= 0\).
Define
on the center manifold \(C_{0}\), and we have
where
and z and zÌ„ are the local coordinates for the center manifold \(C_{0}\) in the direction of \(q^{ *} \) andÂ \(\bar{q}^{*}\). Noting that W is also real if \(u_{t}\) is real, we consider real solutions. For solutions \(u_{t} \in C_{0}\) of Eq. (3.1),
We define this equation as
That is,
where
Noticing \(u_{t}(\theta) = (x_{t}(\theta),y_{t}(\theta)) = W(t,\theta) + zq(\theta) + \bar{z}\bar{q}(\theta)\) and \(q(\theta) = (1,\alpha )^{T}e^{i\omega^{ *} \tau_{1_{0}}\theta} \) by Eq. (3.9), we have
Then from Eq. (3.12) we have
Comparing the coefficients with Eq. (3.12), we obtain
Since there are \(W_{20}(\theta)\) and \(W_{11}(\theta)\) in \(g_{21}\), in the sequel, we shall compute these quantities. From Eqs. (3.8) and (3.9), we have
where
Comparing the coefficients, we obtain
From Eq. (3.13), we know that for \(\theta\in[  1,0)\),
Comparing the coefficients with Eq. (3.14) gives
and
From Eqs. (3.15), (3.18) and the definition of A, it follows that
Notice that \(q(\theta) = (1,\alpha)^{T}e^{i\omega^{ *} \tau _{1_{0}}\theta} \), hence
where \(E_{1} = (E_{1}^{(1)},E_{1}^{(2)})^{T} \in R^{2}\) is a constant vector. Similarly, from Eqs. (3.16) and (3.19), we obtain
where \(E_{2} = (E_{2}^{(1)},E_{2}^{(2)})^{T} \in R^{2}\) is also a constant vector.
In what follows, we shall seek appropriate \(E_{1}\) and \(E_{2}\) in Eqs. (3.21) and (3.23), respectively. It follows from the definition of A and Eqs. (3.18), (3.19) that
and
where \(\eta(\theta) = \eta(0,\theta)\). From Eqs. (3.15) and (3.16) we have
where
Noting that
and substituting Eqs. (3.21) and (3.26) into Eq. (3.24), we have
That is,
It follows that
with
where
Similarly, substituting Eqs. (3.22) and (3.27) into Eq. (3.25), we have
that is,
It follows that
where
From Eqs. (3.21), (3.23), (3.28), (3.29), we can determine \(g_{21}\) and derive the following values:
These formulas describe the periodic solutions of Eq. (3.1) at \(\tau= \tau_{1_{0}}\) on the center manifold. From the discussion above, we have the following result.
Theorem 3.1
The direction of Hopf bifurcation is determined by the sign of \(\mu_{2}\): if \(\mu_{2} > 0\) (\(\mu_{2} < 0\)), then the Hopf bifurcation is supercritical (subcritical). The stability of the bifurcating periodic solutions is determined by the sign of \(\beta _{2}\): if \(\beta_{2} < 0\) (\(\beta_{2} > 0\)), the bifurcating periodic solutions are stable (unstable). The period of the bifurcating periodic solutions is determined by the sign of \(T_{2}\): if \(T_{2} > 0\) (\(T_{2} < 0\)), the bifurcating periodic solutions increase (decrease).
4 Numerical examples
In this section, we present some numerical solutions by using Matlab 7.0 to verify the analytical predictions obtained in the previous section, using the hybrid control strategy to gain control of the Hopf bifurcation of a delayed LotkaVolterra predatorprey system (1.2).
For comparison, the same parameters in Xu et al. [13] are adopted: \(r_{1} = r_{2} = 0.5\), \(a_{11} = 0.5\), \(a_{12} = 1\), \(a_{21} = 1\), \(a_{22} = 1\).
For \(\alpha= 1\) and \(\beta= 0\), system (1.3) becomes the uncontrolled system (1.2). The Hopf bifurcation analysis about this uncontrolled system was presented by Xu et al. [13]. It is known that system (1.2) has a positive equilibrium at \(E_{*}(x^{0},y^{0}) = (\frac{2}{3}, \frac{1}{6})\).
For \(\tau_{1} = 0\), we obtain \(\omega_{0} \approx0.4509\), \(\tau_{2}^{0} \approx3.357\). From Lemma 2.2, we know the positive equilibrium \(E_{*}(x^{0},y^{0}) = (\frac{2}{3}, \frac{1}{6})\) is unstable for \(\tau_{2} \ge\tau_{2}^{0}\), when \(\tau_{2} = 3.7 > \tau_{2}^{0}\), which is illustrated in FigureÂ 1.
For \(\tau_{2} = 3\), we obtain \(\tau_{1}^{0} \approx0.6673\), the positive equilibrium \(E_{*}(x^{0},y^{0}) = (\frac{2}{3}, \frac{1}{6})\) is unstable for \(\tau_{1} \ge\tau_{1}^{0}\), when \(\tau_{1} = 0.8 > \tau_{1}^{0}\), which is illustrated in FigureÂ 2.
Now appropriate Î±, Î² are chosen to control system (1.2). Let us consider the following system:
According to the hybrid control strategy, we can easily make the Hopf bifurcation of the uncontrolled system (1.2) disappear, as illustrated in FiguresÂ 3 and 4. It is illustrated that the onset of Hopf bifurcation is delayed when the hybrid controller has been incorporated into the model.
For \(\tau_{1} = 0\), we obtain \(\omega_{0} \approx0.1764\), \(\tau_{2_{0}} \approx4.5037\). From Lemma 2.2, we know the controlled system (1.3) undergoes a Hopf bifurcation at \(E^{ *} (x^{ *},y^{ *} )\) when \(\tau _{2} = \tau_{2_{0}}\). For \(\tau_{2} = 4.6 > \tau_{2_{0}}\), the solution is illustrated in FigureÂ 5.
For \(\tau_{2} = 3\), we obtain \(\tau_{1_{0}} \approx2.443\). According to Theorem 2.1, the controlled system (1.3) undergoes a Hopf bifurcation at \(\tau_{1_{0}} \approx2.443\). From Eq. (3.30), we obtain \(c_{1}(0) =  0.2954  0.4505i \), \(\mu_{2} = 10.4382\), \(\beta_{2} =  0.5908\), \(T_{2} = 0.2761\). According to Theorem 3.1, Hopf bifurcation is supercritical, the bifurcation periodic solution exists for \(\tau_{1} > \tau_{1_{0}}\) and it is unstable. For \(\tau_{1} = 2.8 > \tau_{1_{0}}\), the solution is illustrated in FigureÂ 6.
Remark 4.1
For \(\alpha= 1\), \(\beta= 0.1\) in the controlled system (1.3), then we obtain a control model only based on delayed feedback. Take case (b) for example, when \(\tau_{1} = 0\), by calculation, we have \(\omega_{0} \approx0.2963\), \(\tau_{2_{0}} \approx2.6612\), the onset of an inherent bifurcation about uncontrolled system (1.2) is not delayed (see FigureÂ 7). It is demonstrated that the hybrid control strategy is more suitable than feedback control of system (1.2) in this paper.
These numerical simulation solutions constitute excellent validation of the new theoretical formulation and analysis presented in this paper. Compared with a general statefeedback control, the hybrid control established here can be more effective in varying the location of the Hopf bifurcation point while considering parametric disturbance. Therefore, a more practical method for controlling Hopf bifurcation is established.
5 Conclusions
In this paper, an efficient hybrid control strategy of Hopf bifurcation for a LotkaVolterra predatorprey model with two delays has been investigated. By determining an appropriate control parameter, we are able to delay the onset of Hopf bifurcation. For \(\tau_{2} = 3\), the critical value of delay increases from \(\tau_{1_{0}} \approx0.6673\) to 2.443. By using the normal form theory and center manifold theorem, the explicit formulas which determine the direction of Hopf bifurcation and stability of the bifurcating periodic solution of the controlled system are derived. The numerical solutions for supercritical Hopf bifurcation and stable bifurcation periodic solutions are in excellent agreement with theoretical analysis. From biology viewpoint, stable bifurcation periodic solutions imply coexistence of both species in an oscillatory mode.
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Acknowledgements
The authors would like to thank the referees for the careful reading of the manuscript and valuable suggestions. This work was supported by the National Nature Science foundation of China (11472116, 11472115), Postgraduate Research & Practice Innovation Program of Jiangsu Province (5561190004, 4061190009) and Qinglan project of Jiangsu.
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Peng, M., Zhang, Z. & Wang, X. Hybrid control of Hopf bifurcation in a LotkaVolterra predatorprey model with two delays. Adv Differ Equ 2017, 387 (2017). https://doi.org/10.1186/s1366201714345
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DOI: https://doi.org/10.1186/s1366201714345