- Research
- Open Access
- Published:

# Note on the persistence and stability property of a stage-structured prey–predator model with cannibalism and constant attacking rate

*Advances in Difference Equations*
**volume 2020**, Article number: 75 (2020)

## Abstract

We revisit the persistence and stability property of a stage-structured prey–predator model with cannibalism and constant attacking rate. By using the differential inequality theory and Bendixson–Dulac criterion, we show that if the system without cannibalism is permanent, then the system with cannibalism is also permanent. By developing some new analysis technique, we obtain a new set of sufficient conditions which ensure the global asymptotic stability of the nonnegative equilibrium, which means that, under some suitable assumption, prey cannibalism has no influence on the stability property of the predator free equilibrium. Our results essentially improve the corresponding results of Limin Zhang and Chaofeng Zhang.

## Introduction

During the last decades, mathematical biology has become one of the important research areas [1–40]. Specially, many scholars investigated the dynamic behaviors of the stage-structured ecosystem, see [1–21, 39, 40], and the references cited therein.

In constructing the stage-structured model, some scholars [1–12] argued that a suitable stage-structured model should incorporate time delay, which reflects the period it takes to immature species to grow up to mature species. For example, Chen et al. [1] and Chen et al. [2] studied the persistence and extinction property of a stage-structured predator–prey system (stage structure for both predator and prey, respectively), they found that due to the influence of stage structure, the extinction of predator species could not directly imply the permanence of the prey species; the extinction of prey species could not lead to the extinction of predator species. Such a phenomenon could not be observed in the predator–prey system without stage structure. They argued that the reason maybe due to the assumption of the system that the predator species has another food resource. Also, Chen et al. [4] showed that due to the influence of the stage structure, the cooperative system could be driven to extinction.

Some scholars [13–21, 39, 40] also proposed and studied the stage-structured ecosystem without time delay, they assumed that there are proportional numbers of immature species that become mature species at time *t*. For example, Lei[16] proposed the following stage-structured commensalism system:

He found that if the stage-structured species (i.e., the first species) is extinct, then, depending on the intensity of cooperation, the species may still be extinct or become persistent. If the stage-structured species is permanent, then the final system is always globally asymptotically stable. Thus, he drew the conclusion that increasing the intensity of cooperation between the species is one of the very useful methods to avoid the extinction of the endangered species. Xu, Chaplain, and Davidson [40] proposed the following stage-structured prey–predator model:

where \(x_{1}(t)\) represents the density of immature individual preys at time *t* and \(x_{2}(t)\) denotes the density of mature individual preys at time *t*, \(y(t)\) represents the density of the predator at time *t*. One could refer to [40] for more details about the construction of the system. Concerned with the persistence property of the system, the authors obtained the following result.

### Theorem A

*System* (1.2) *is uniformly persistent provided that*

- (\(H_{1}\)):
- $$ a_{2}>d_{3}, $$(1.3)
- (\(H_{2}\)):
- $$ \frac{b_{1}g}{g+d_{1}}> \frac{a_{1}}{m}. $$(1.4)

Cannibalism, which is the act of eating offspring, is observed to occur in some fish [41] and in some spiders [42]. Thus, incorporating cannibalism in the stage-structured models is more realistic and has more practical significance for some cannibals. Based on the work of Xu et al. [40], Zhang and Zhang [39] proposed the following stage-structured prey–predator model with cannibalism for prey and constant attacking rate for predator:

where all the coefficients have the same meaning as that of system (1.2). \(b_{2}\) denotes the cannibalism attacking rate of the mature prey population; *s* is the conversion rate of the immature prey into the mature prey due to cannibalism, according to the biological meaning, \(s < 1\). Concerned with the persistence property of system (1.5), the authors obtained the following result.

### Theorem B

*System* (1.5) *is permanent provided that*

- (\(H_{3}\)):
- $$ a_{2}>d_{3}, $$(1.6)
- (\(H_{4}\)):
- $$ \frac{g}{g+d_{1}}> \max \biggl\{ \frac{a_{1}}{b_{1}m},s \biggr\} $$(1.7)

*hold*.

System (1.5) always admits a predator free equilibrium \(E_{1}(\overline{x}_{1},\overline{x}_{2},0)\), where

here \(\delta =(g+d_{1})d_{2}-sb_{2}\).

Concerned with the stability property of the nonnegative equilibrium \(E_{1}(\overline{x}_{1},\overline{x}_{2},0)\), the authors obtained the following result (Theorem 3.3 in [39]).

### Theorem C

*Assume that*

- (\(H_{5}\)):
- $$ a_{2}< d_{3}, $$(1.9)
- (\(H_{6}\)):
- $$ \frac{g}{g+d_{1}}> \max \biggl\{ \frac{a_{1}}{b_{1}m},s \biggr\} $$(1.10)

*hold*, *then the nonnegative equilibrium*\(E_{1}(\overline{x}_{1}, \overline{x}_{2},0)\)*is globally asymptotically stable*.

Here, several interesting issues are proposed as follows:

- 1.
Condition (1.7) is independent of coefficient \(b_{2}\); however, \(b_{2}\) denotes the cannibalism attacking rate of the mature prey population. Hence, the condition of Theorem B seems curious.

- 2.
Comparing Theorems A and B, we found that to ensure permanence of system (1.5), one needs to require

$$ s< \frac{g}{g+d_{1}} $$(1.11)holds, what would happen if

$$ s\geq \frac{g}{g+d_{1}} $$(1.12)holds?

- 3.
Conditions (1.9) and (1.10) are independent of coefficient \(b_{2}\). Does \(b_{2}\) really have no influence on the stability property of the nonnegative equilibrium?

- 4.
In Theorem C, the authors only considered the case

$$ s< \frac{g}{g+d_{1}}, $$(1.13)what would happen if

$$ s\geq\frac{g}{g+d_{1}} $$(1.14)holds?

To find out the answer to the above issues, it seems better for us to consider some numeric examples, which may give some hints.

### Example 1.1

Consider the following system:

Here, we choose \(b_{1}=4\), \(m=1\), \(s=\frac{1}{2}\), \(d_{1}=1\), \(g=3\), \(a_{2}=1\), \(d _{3}=\frac{1}{4}\), \(d_{2}=1\), \(b_{2}=10\). Hence,

That is, the conditions of Theorem B hold. Also, here we choose \(b_{2}=10\), which is very large when compared to the other coefficients. Numeric simulations (Figs. 1–3) show that in this case the system is permanent. Hence, we conjecture that the cannibalism attacking rate of the mature prey population has no influence on the persistence property of the system if the system without cannibalism is permanent.

### Example 1.2

Consider the following system:

Here, we choose \(b_{1}=4\), \(m=2\), \(s=\frac{3}{4}\), \(d_{1}=1\), \(g=1\), \(a_{2}=1\), \(d _{3}=\frac{1}{4}\), \(d_{2}=1\), \(b_{2}=1\), \(a_{1}=2\), hence

However,

That is, the conditions of Theorem A hold, while the second inequality in Theorem B does not hold. Numeric simulations (Figs. 4–6) show that in this case the system is permanent.

Example 1.2 shows that maybe parameter *s* is not an essential coefficient to ensure the permanence of system (1.5), while Example 1.1 shows that maybe parameter \(b_{2}\) is not an essential coefficient to ensure the permanence of system (1.5). This leads us to making the following conjecture.

### Conjecture A

Maybe in system (1.5) cannibalism has no influence on the persistence property of the system.

### Example 1.3

Consider the following system:

Here, we choose \(b_{1}=4\), \(m=2\), \(s=\frac{3}{4}\), \(d_{1}=1\), \(g=1\), \(a_{2}= \frac{1}{2}\), \(d_{3}=\frac{1}{4}\), \(d_{2}=1\), \(b_{2}=1\), \(a_{1}=2\), \(d_{3}=1\), hence

However,

That is, the first inequality in Theorem C holds, while the second inequality in Theorem C does not hold. Numeric simulations (Figs. 7–9) show that in this case the nonnegative equilibrium \(E_{1}(2.246211251, 2.246211251,0)\) is still globally asymptotically stable.

Example 1.3 shows that maybe parameter *s* is not an essential coefficient to ensure the stability of the nonnegative equilibrium of system (1.1). This leads us to proposing the following conjecture.

### Conjecture B

In Theorem C, inequality (1.13) is not an essential one, maybe it is redundant and could be dropped.

The aim of this paper is to give an affirmative answer to the above two conjectures. Indeed, we will establish the following results.

### Theorem 1.1

*Assume that* (\(H_{1}\)) *and* (\(H_{2}\)) *hold*, *then system* (1.5) *is permanent*.

### Remark 1.1

Compared with Theorem A, B, and 1.1, Theorem 1.1 shows that if the system without cannibalism is permanent, then cannibalism has no influence on the persistence property of the system.

### Theorem 1.2

*Assume that* (\(H_{5}\)) *and* (\(H_{2}\)) *hold*, *then the nonnegative equilibrium*\(E_{1}(\overline{x}_{1}, \overline{x} _{2}, 0)\)*of system* (1.5) *is globally asymptotically stable*.

### Remark 1.2

Compared with Theorem C and Theorem 1.2, our result shows that under assumptions (\(H_{1}\))and (\(H_{2}^{\prime }\)) cannibalism has no influence on the stability property of the boundary equilibrium of system (1.5).

We prove Theorems 1.1 and 1.2 in the next section and Sect. 3, respectively. We end this paper with a brief discussion.

## Proof of Theorem 1.1

Before we begin the proof of Theorem 1.1, we need to establish some useful lemmas.

We first introduce lemmas from [39], which give the upper bound of the solutions of system (1.5).

### Lemma 2.1

*Any solutions of system* (1.5) *with positive initial conditions are ultimately bounded*.

### Lemma 2.2

*Consider the following system*:

*Under the assumption of Theorem *1.1, *system* (2.1) *admits a boundary equilibrium*\(E_{0}(0,0)\), *which is a saddle point*, *and a positive equilibrium*\(E^{*}(u_{1}^{*}, u_{2}^{*})\), *which is locally asymptotically stable and globally asymptotically stable*.

### Proof

The equilibria of system (2.1) satisfy the equations

Obviously, under the assumption of Theorem 1.1, the system admits the boundary equilibrium \(E_{0}(0,0)\) and the unique positive equilibrium \(E^{*}(u_{1}^{*},u_{2}^{*})\), where

where

The variation matrix of the continuous-time system (2.1) at an equilibrium solution \((u_{1},u_{2})\) is

Thus, at \(E_{0}(0,0)\)

Consequently, the characteristic equation is

Note that from condition (\(H_{2}\)) one has

hence, Eq. (2.6) has one positive solution, that is, \(J(0,0)\) has one positive eigenvalue, hence \(E_{0}(0,0)\) is unstable.

At \(E^{*}(u_{1}^{*},u_{2}^{*})\)

Note that

and

Since

then

It follows from (2.7) and (2.8) that both eigenvalues of \(J(u_{1}^{*},u _{2}^{*})\) have negative real parts; consequently, this steady-state solution is locally asymptotically stable.

In what follows, we will take the idea and method of Wu and Chen[38] to investigate the global asymptotic stability property of the positive equilibrium. We need to determine the existence or non-existence of the limit cycle in the first quadrant.

For \(E^{*}(u_{1}^{*},u_{2}^{*})\), which is the unique stable equilibrium in the first quadrant, let *AB* be the line segment of \(L_{1}:u_{1}=p\) and *BC* be the line segment of \(L_{2}:u_{2}=q\), where \(A(p,0)\), \(B(p,q)\), \(C(0,q)\), and *p*, *q* are positive constants which satisfy \(p>u_{1}^{*}\), and

By simple calculation, we have

thus *AB*, *BC* are the transversals of system (2.1). It is not hard to check that *OA*, *OC* are the transversals of system (1.1), and any trajectory enters region *OABCO* from its exterior to interior.

Let \(G= \frac{1}{u_{1}u_{2}}\), it follows from (2.1) that

By Poincare–Bendixson theorem, there are no limit cycles in the first quadrant, thus \(E_{*}(x_{1}^{*},x_{2}^{*})\) is globally asymptotically stable if it exists. This ends the proof of Lemma 2.2. □

Now we are in a position to prove Theorem 1.1.

### Proof of Theorem 1.1

Let \((x_{1}(t), x_{2}(t), y(t))\) be any positive solution of system (1.5), its initially condition is \((x_{1}(0),x_{2}(0), y(0))\). From system (1.5) it immediately follows that

Now let us consider the following auxiliary system:

Let \((u_{1}(t), u_{2}(t))\) be the positive solution of system (2.10) that satisfies the initial condition \((u_{1}(0),u_{2}(0))=(x_{1}(0),x_{2}(0))\). Then, by the standard comparison argument, it follows that

It follows from Lemma 2.2 that under the assumption of Theorem 1.1 system (2.10) admits a unique positive equilibrium \(E^{*}(u_{1}^{*},u _{2}^{*})\) which is globally asymptotically stable. That is,

Therefore, for \(\varepsilon >0\) small enough, without loss of generality, we may assume that

There exists \(T>0\) such that, for all \(t\geq T\),

Combining with (2.11) and (2.13) leads to

Hence,

It follows from (2.14) that, for *T* large enough, \(x_{2}(t)\geq \frac{1}{2}u_{2}^{*}\). This, together with the third equation of system (1.5), leads to

from (2.16) one could easily obtain that

Lemma 2.1, (2.15), and (2.17) show that system (1.5) is permanent under assumptions (\(H_{1}\)) and (\(H_{2}\)), this ends the proof of Theorem 1.1. □

## Proof of Theorem 1.2

We first establish several lemmas which will be used in the proof of Theorem 1.2.

### Lemma 3.1

*Consider the following system*:

*Assume that*

*holds*, *then system* (3.2) *admits a boundary equilibrium*\(E_{0}(0,0)\), *which is a saddle point*, *and a positive equilibrium*\(E^{*}(u_{1}^{*}, u_{2}^{*})\), *which is locally asymptotically stable and globally asymptotically stable*.

### Proof

The proof of this lemma is similar to the proof of Lemma 2.2, with some minor revision, and we omit the details here. □

### Lemma 3.2

*Consider the following system*:

*System* (3.2) *admits a globally asymptotically stable positive equilibrium*\(E_{*}(\overline{x}_{1},\overline{x}_{2})\), *where*\(\overline{x}_{1}\), \(\overline{x}_{2}\)*is defined by* (1.2).

Now we are in a position to prove Theorem 1.2.

### Proof of Theorem 1.2

Let \((x_{1}(t), x_{2}(t), y(t))\) be a positive solution of system (1.5) with initial conditions \(x_{1}(0)>0\), \(x_{2}(0)>0\), \(y(0)>0\).

It follows from the third equation of system (1.1) that

hence

Thus, under the assumption \(a_{2}< d_{3}\), we have

From the first two equations of system (1.5), we have

Now let us consider the following auxiliary equation:

By Lemma 3.2, system (3.6) has a unique globally attractive positive equilibrium \(E_{*}(\overline{x}_{1},\overline{x}_{2})\). Let \((u_{1}(t), u_{2}(t))\) be the solution of system (3.6) with \((u_{1}(0),u_{2}(0))=(x_{1}(0),x_{2}(0))\), by comparison theorem, we have

Moreover, from the global asymptotic stability of \(E_{2}(\overline{x} _{1},\overline{x}_{2})\), for any small enough given *ε* (\(0< \varepsilon <1\)), there exists \(T_{1} >0\) such that

Equation (3.8) combined with (3.7) leads to

Hence,

Since *ε* is arbitrary small enough positive constant, setting \(\varepsilon \rightarrow 0\) in (3.10) leads to

From the first two equations of system (1.5), we also have

Now let us consider the following auxiliary equation:

From (1.4) and Lemma 3.1, system (3.12) has a unique globally attractive positive equilibrium \(E^{*}(v_{1}^{*},v_{2}^{*})\). Let \((v_{1}(t), v _{2}(t))\) be the solution of system (3.12) with \((v_{1}(0),v_{2}(0))=(x _{1}(0),x_{2}(0))\), by comparison theorem, we have

Moreover, from the global asymptotic stability of \(E^{*}(v_{1}^{*},v _{2}^{*})\), for any small enough given *ε* (\(0<\varepsilon <\frac{1}{2}v_{i}^{*}\)), there exists \(T_{2} >T_{1}\) such that

Equation (3.14) combined with (3.13) leads to

For any small enough positive constant \(\varepsilon _{1}\) (\(0< \varepsilon _{1}< \frac{a_{1}}{m}\)), from (3.4) and (3.15), there exists \(T_{3}>T_{2}\) such that, for all \(t\geq T_{3}\),

holds. From (3.16) and the first and second equations of system (1.5), we have

Now let us consider the following auxiliary equation:

Condition (1.4) implies that

Hence, by Lemma 3.1, system (3.18) has a unique globally attractive positive equilibrium \(E_{\varepsilon _{1}}(w_{1}^{\varepsilon _{1}},w _{2}^{\varepsilon _{1}})\), where

where \(\delta _{1}=-b_{1}b_{2}s+b_{2}\varepsilon _{1}+d_{2}(d_{1}+g)\). Obviously,

where *δ* is defined by (1.8), and

Hence, it follows from (3.20)–(3.22) that

where \(\overline{x}_{1}\), \(\overline{x}_{2}\) are defined by (1.8).

Let \((w_{1}(t), w_{2}(t))\) be the solution of system (3.18) with \((w_{1}(0),w_{2}(0))=(x_{1}(0),x_{2}(0))\). By the comparison theorem, we have

Moreover, from the global asymptotic stability of \(E_{\varepsilon _{1}}(w _{1}^{*\varepsilon _{1}},w_{2}^{*\varepsilon _{1}})\), for above \(\varepsilon _{1}\), there exists \(T_{3} >T_{2}\) such that

Equation (3.24) combined with (3.25) leads to

Hence,

Since \(\varepsilon _{1}\) is arbitrary small enough positive constant, setting \(\varepsilon _{1}\rightarrow 0\) in (3.27), it follows from (3.23) that

Equation (3.11) together with (3.27)leads to

That is,

Equation (3.4) and (3.29) show that the nonnegative equilibrium \(E_{1}( \overline{x}_{1},\overline{x}_{2},0)\) of system (1.5) is globally asymptotically stable. This ends the proof of Theorem 1.2. □

## Conclusion

Based on the work of Xu et al. [40], Zhang and Zhang [39] tried to incorporate the cannibalism to system (1.1), and they proposed system (1.5). By constructing some suitable Lyapunov function, they obtained the conditions (Theorem B) which ensure the permanence of system (1.5). The condition is independent of \(b_{2}\), which leads us to finding out the reason behind this phenomenon. By numeric simulations (Example 1.1 and 1.2), we found that maybe both coefficients \(b_{2}\) and *s* have no influence on the persistence property of the system. Indeed, we propose a conjecture (Conjecture A). Obviously, one could not prove this conjecture by directly applying the method of [39, 40]. By developing the analysis technique of Wu et al. [13], we finally give a strict proof of Theorem 1.1. Obviously, Theorem 1.1 essentially improves the main result of [39] since our condition is cannibalism independent, which means that if the original system is permanent, then cannibalism has no influence on the persistence property of the system.

Concerned with the stability property of the predator free equilibrium, Zhang and Zhang[39] obtained Theorem C, which is cannibalism dependent. However, numeric simulations (Example 1.3) show that their result still has room to improve. We first propose a conjecture (Conjecture B), then, by developing the analysis technique of differential inequality theory, we finally establish some new result about the stability property of the predator free equilibrium, some unnecessary restriction of Theorem C is dropped. Obviously, Theorem 1.2 essentially improves the main result of [39] since our condition is cannibalism independent, which means that if inequalities (\(H_{5}\))and (\(H_{2}\)) hold, cannibalism has no influence on the persistence property of the system.

## References

- 1.
Chen, F.D., Chen, W.L., et al.: Permanence of a stage-structured predator–prey system. Appl. Math. Comput.

**219**(17), 8856–8862 (2013) - 2.
Chen, F.D., Xie, X.D., et al.: Partial survival and extinction of a delayed predator–prey model with stage structure. Appl. Math. Comput.

**219**(8), 4157–4162 (2012) - 3.
Chen, F.D., Wang, H.N., Lin, Y.H., Chen, W.L.: Global stability of a stage-structured predator–prey system. Appl. Math. Comput.

**223**, 45–53 (2013) - 4.
Chen, F.D., Xie, X.D., et al.: Dynamic behaviors of a stage-structured cooperation model. Commun. Math. Biol. Neurosci.

**2015**, Article ID 4 (2015) - 5.
Li, T.T., Chen, F.D., et al.: Stability of a mutualism model in plant-pollinator system with stage-structure and the Beddington-DeAngelis functional response. J. Nonlinear Funct. Anal.

**2017**, Article ID 50 (2017) - 6.
Chen, F., Huang, X., Deng, H.: Dynamic behaviors of a stage structure single species model with cannibalism. Appl. Math. E-Notes

**19**, 469–475 (2019) - 7.
Li, Z., Han, M.A., et al.: Global stability of stage-structured predator–prey model with modified Leslie-Gower and Holling-type II schemes. Int. J. Biomath.

**6**, Article ID 1250057 (2012) - 8.
Li, Z., Han, M., et al.: Global stability of a predator–prey system with stage structure and mutual interference. Discrete Contin. Dyn. Syst., Ser. B

**19**(1), 173–187 (2014) - 9.
Lin, X., Xie, X., et al.: Convergences of a stage-structured predator–prey model with modified Leslie-Gower and Holling-type II schemes. Adv. Differ. Equ.

**2016**(1), 181 (2016) - 10.
Pu, L.Q., Miao, Z.S., et al.: Global stability of a stage-structured predator–prey model. Commun. Math. Biol. Neurosci.

**2015**, Article ID 5 (2015) - 11.
Han, R.Y., Yang, L.Y., et al.: Global attractivity of a single species stage-structured model with feedback control and infinite delay. Commun. Math. Biol. Neurosci.

**2015**, Article ID 6 (2015) - 12.
Ma, Z.H., Li, Z.Z., Wang, S.F., Li, T., Zhang, F.P.: Permanence of a predator–prey system with stage structure and time delay. Appl. Math. Comput.

**201**, 65–71 (2008) - 13.
Xiao, Z., Li, Z., Zhu, Z., et al.: Hopf bifurcation and stability in a Beddington-DeAngelis predator–prey model with stage structure for predator and time delay incorporating prey refuge. Open Math.

**17**(1), 141–159 (2019) - 14.
Khajanchi, S., Banerjee, S.: Role of constant prey refuge on stage structure predator–prey model with ratio dependent functional response. Appl. Math. Comput.

**314**, 193–198 (2017) - 15.
Chen, F., Guan, X., Huang, X., et al.: Dynamic behaviors of a Lotka–Volterra type predator–prey system with Allee effect on the predator species and density dependent birth rate on the prey species. Open Math.

**17**(1), 1186–1202 (2019) - 16.
Xue, Y., Pu, L., et al.: Global stability of a predator–prey system with stage structure of distributed-delay type. Commun. Math. Biol. Neurosci.

**2015**, Article ID 12 (2015) - 17.
Huang, X., Chen, F., Xie, X., et al.: Extinction of a two species competitive stage-structured system with the effect of toxic substance and harvesting. Open Math.

**17**(1), 856–873 (2019) - 18.
Yue, Q.: Permanence of a delayed biological system with stage structure and density-dependent juvenile birth rate. Eng. Lett.

**27**(2), 1–5 (2019) - 19.
Lei, C.: Dynamic behaviors of a stage-structured commensalism system. Adv. Differ. Equ.

**2018**(1), 301 (2018) - 20.
Lei, C.Q.: Dynamic behaviors of a stage structure amensalism system with a cover for the first species. Adv. Differ. Equ.

**2018**(1), 272 (2018) - 21.
Xiao, A., Lei, C.Q.: Dynamic behaviors of a non-selective harvesting single species stage structure system incorporating partial closure for the populations. Adv. Differ. Equ.

**2018**(1), 245 (2018) - 22.
Lei, C.Q.: Dynamic behaviors of a non-selective harvesting May cooperative system incorporating partial closure for the populations. Commun. Math. Biol. Neurosci.

**2018**, Article ID 12 (2018) - 23.
Lin, Q., Xie, X., et al.: Dynamical analysis of a logistic model with impulsive Holling type-II harvesting. Adv. Differ. Equ.

**2018**(1), 112 (2018) - 24.
Xie, X., Xue, Y., et al.: Permanence and global attractivity of a nonautonomous modified Leslie-Gower predator–prey model with Holling-type II schemes and a prey refuge. Adv. Differ. Equ.

**2016**, 184 (2016) - 25.
Xie, X.D., Chen, F.D., et al.: Note on the stability property of a cooperative system incorporating harvesting. Discrete Dyn. Nat. Soc.

**2014**, Article ID 327823 (2014) - 26.
Wu, R., Li, L., et al.: A Holling type commensal symbiosis model involving Allee effect. Commun. Math. Biol. Neurosci.

**2018**, Article ID 6 (2018) - 27.
Xue, Y., Xie, X., et al.: Global attractivity and extinction of a discrete competitive system with infinite delays and single feedback control. Discrete Dyn. Nat. Soc.

**2018**, Article ID 1893181 (2018) - 28.
Lin, Q.: Allee effect increasing the final density of the species subject to the Allee effect in a Lotka–Volterra commensal symbiosis model. Adv. Differ. Equ.

**2018**(1), 196 (2018) - 29.
Lin, Q.: Stability analysis of a single species logistic model with Allee effect and feedback control. Adv. Differ. Equ.

**2018**(1), 190 (2018) - 30.
Liu, Y., Xie, X., Lin, Q.: Permanence, partial survival, extinction, and global attractivity of a nonautonomous harvesting Lotka–Volterra commensalism model incorporating partial closure for the populations. Adv. Differ. Equ.

**2018**(1), 211 (2018) - 31.
Chen, L., Wang, Y., et al.: Influence of predator mutual interference and prey refuge on Lotka–Volterra predator–prey dynamics. Commun. Nonlinear Sci. Numer. Simul.

**18**(11), 3174–3180 (2013) - 32.
He, M., Chen, F.: Extinction and stability of an impulsive system with pure delays. Appl. Math. Lett.

**91**, 128–136 (2019) - 33.
He, M., Li, Z., et al.: Dynamics of an impulsive model of plankton allelopathy with delays. J. Appl. Math. Comput.

**55**(1–2), 749–762 (2017) - 34.
Zhao, L., Qin, B., et al.: Permanence and global stability of a May cooperative system with strong and weak cooperative partners. Adv. Differ. Equ.

**2018**, 172 (2018) - 35.
Yang, K., Miao, Z.S., et al.: Influence of single feedback control variable on an autonomous Holling-II type cooperative system. J. Math. Anal. Appl.

**435**(1), 874–888 (2016) - 36.
Chen, F., Xie, X., et al.: Extinction in two species nonautonomous nonlinear competitive system. Appl. Math. Comput.

**274**, 119–124 (2016) - 37.
Chen, B.: Dynamic behaviors of a non-selective harvesting Lotka–Volterra amensalism model incorporating partial closure for the populations. Adv. Differ. Equ.

**2018**, 111 (2018) - 38.
Wu, H.L., Chen, F.D.: Harvesting of a single-species system incorporating stage structure and toxicity. Discrete Dyn. Nat. Soc.

**2009**, Article ID 290123 (2009) - 39.
Zhang, L., Zhang, C.: Rich dynamic of a stage-structured prey–predator model with cannibalism and periodic attacking rate. Commun. Nonlinear Sci. Numer. Simul.

**15**(12), 4029–4040 (2010) - 40.
Xu, R., Chaplain, M.A.J., Davidson, F.A.: Persistence and global stability of a ratio-dependent predator–prey model with stage structure. Appl. Math. Comput.

**158**, 729–744 (2004) - 41.
Smith, C., Reay, P.: Cannibalism in teleost fish. Rev. Fish Biol. Fish.

**1**, 41–54 (1991) - 42.
Rickers Schen, S.: Cannibalism in Paradosa palustris (Araneae, Lycosidae): effects of alternative prey, habitat structure, and density. Basic Appl. Ecol.

**6**, 471–478 (2005)

### Acknowledgements

The authors would like to thank Dr. Liqiong Pu for bringing to our attention the paper of Jiming Zhang.

### Availability of data and materials

Data sharing not applicable to this article as no datasets were generated or analysed during the current study.

## Funding

The research was supported by the National Natural Science Foundation of China under Grant (11601085).

## Author information

### Affiliations

### Contributions

All authors contributed equally to the writing of this paper. All authors read and approved the final manuscript.

### Corresponding author

## Ethics declarations

### Ethics approval and consent to participate

Not applicable.

### Competing interests

The authors declare that there is no conflict of interests.

### Consent for publication

Not applicable.

## Additional information

### Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

## Rights and permissions

**Open Access** This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

## About this article

### Cite this article

Chen, F., Deng, H., Zhu, Z. *et al.* Note on the persistence and stability property of a stage-structured prey–predator model with cannibalism and constant attacking rate.
*Adv Differ Equ* **2020, **75 (2020). https://doi.org/10.1186/s13662-020-02546-8

Received:

Accepted:

Published:

DOI: https://doi.org/10.1186/s13662-020-02546-8

### Keywords

- Stage structure
- Predator–prey
- Cannibalism
- Permanence
- Global asymptotical stability