Skip to main content

Theory and Modern Applications

The influence of partial closure for the populations to a non-selective harvesting Lotka–Volterra discrete amensalism model

Abstract

In this paper, a non-selective harvesting Lotka–Volterra amensalism discrete model incorporating partial closure for the populations is proposed and studied. By applying the relevant conclusions of difference inequality and some calculation technique, sufficient conditions are obtained to ensure the permanence and extinction of the system. By constructing a suitable Lyapunov function, sufficient conditions that ensure the global attractivity of the system are obtained. Finally, numerical simulations show the feasibility of our results.

1 Introduction

During the last decade, the study of dynamic behaviors of the amensalism model has become one of the most important research topics, see [1,2,3,4,5,6,7,8,9,10,11,12]; here, amensalism means that a species inflicts harm on other species without any costs or benefits received by the other. Such topics as the stability of the equilibrium [1, 3,4,5, 8], the existence of the positive periodic solution [2, 9, 11], the extinction of the species [8, 10], the influence of the cover [8, 12], the influence of the functional response [10], etc. have been extensively studied. Recently, Xiong et al. [1] proposed the following amensalism model:

$$ \textstyle\begin{cases} \frac{dN_{1}}{dt}=r_{1}N_{1} (1- \frac{N_{1}}{P_{1}}-u \frac{N_{2}}{P_{1}} ), \\ \frac{dN_{2}}{dt}=r_{2}N_{2} (1- \frac{N_{2}}{P_{2}} ), \end{cases} $$
(1.1)

where u, \(r_{i}\), \(P_{i}\), \(i = 1, 2\), are all positive constants. They investigated the local stability property of the equilibria of system (1.1).

On the other hand, as was pointed out by Chakraborty et al. [13], the study of resource management, including fisheries, forestry, and wildlife management, is very important. They argued that it is necessary to harvest the population, but harvesting should be regulated so that both the ecological sustainability and conservation of the species can be implemented in a long run. Already, they proposed a non-selective harvesting predator-prey system incorporating partial closure for the populations, they investigated the local and global stability property of the system, and some interesting results related to the optimal harvesting were obtained. Recently, Chen [3] proposed the following non-selective harvesting Lotka–Volterra amensalism model incorporating partial closure for the populations:

$$ \textstyle\begin{cases} \frac{dN_{1}}{dt}=r_{1}N_{1} (1- \frac{N_{1}}{P_{1}}-u \frac{N_{2}}{P_{1}} )-q_{1}Em N_{1}, \\ \frac{dN_{2}}{dt}=r_{2}N_{2} (1- \frac{N_{2}}{P_{2}} )-q_{2}EmN_{2}. \end{cases} $$
(1.2)

They investigated the local and global stability of the boundary and interior equilibria. They proved that depending on the fraction of the stock available for harvesting, the system maybe extinction, partial survival, or two species may coexist in a stable state.

As we all know, though most dynamic behaviors of population models are based on the continuous models governed by differential equations, the discrete time models governed by difference equation are more appropriate than the continuous ones when the size of the population is rarely small or the population has non-overlapping generations. It has been found that the dynamic behaviors of the discrete system is rather complex and contains richer dynamics than the continuous ones [14]. Recently, more and more scholars pay attention to studying the discrete population models (see [14,15,16,17,18,19] and the references cited therein).

However, to the best of our knowledge, to this day, seldom did scholars propose and consider the influence of harvesting on the discrete amensalism model. This motivates us to propose and study the discrete system of (1.2). The aim of this paper is to investigate the permanence, extinction, and global attractivity of the following system:

$$ \textstyle\begin{cases} x_{1}(n+1)=x_{1}(n)\exp \{r_{1}(n) (1- \frac{x_{1}(n)}{p_{1}(n)}- \frac{\mu (n)}{p_{1}(n)}x_{2}(n) )-q_{1}(n)Em \}, \\ x_{2}(n+1)=x_{2}(n)\exp \{r_{2}(n) (1- \frac{x_{2}(n)}{p_{2}(n)} )-q_{2}(n)Em \}, \end{cases} $$
(1.3)

where \(x_{1}(n)\), \(x_{2}(n)\) denote the population densities of the two species at any time n. \(r_{i}(p_{i})\) represents the intrinsic growth rate (environmental carrying capacity) of the ith species, \(q_{i}\) is the catchability co-efficient of the two species. E is the combined fishing effort used to harvest, and m (\(0 < m < 1\)) is the fraction of the stock available for harvesting. One could refer to [1, 13, 20] for more background and the adjustment of system (1.3). Throughout this paper, we assume that \(\{\mu (n) \}\), \(\{r_{i}(n) \}\), \(\{p_{i}(n) \}\), \(\{q_{i}(n) \}\) are bounded non-negative almost sequences such that

$$ \begin{aligned} &0< \mu ^{l}\leq \mu (n)\leq \mu ^{u},\qquad 0< r_{i}^{l}\leq r_{i}(n) \leq r _{i}^{u}, \\ &0< p_{i}^{l}\leq p_{i}(n)\leq p_{i}^{u},\qquad 0< q_{i}^{l}\leq q_{i}(n) \leq q_{i}^{u}, \quad i=1,2. \end{aligned} \quad {(H)} $$

Here, for any bounded sequence \(\{a(n) \}\), \(a^{u}= \sup_{n\in N} \{a(n) \}\), \(a^{l}=\inf_{n\in N} \{a(n) \}\).

From the point of view of biology, we assumed that \(x_{i}(0)>0\), (\(i=1,2\)). Then it is easy to see that the solutions of (1.3) with the above initial condition remain positive for all \(n\in N^{+}= \{0,1,2,\ldots \}\).

The organization of this paper is as follows. In Sect. 2, we give some useful lemmas. Sufficient conditions for the permanence and extinction of (1.3) are given in Sect. 3 and Sect. 4. Then, in Sect. 5, we establish sufficient conditions for the global attractivity of (1.3). Some examples together with their numeric simulations are presented in Sect. 6. We end this paper with a brief discussion.

2 Preliminaries

In this section, we will introduce several useful lemmas.

Lemma 2.1

([21])

Assume that \(\{x(k) \}\) satisfies \(x(k)>0\) and

$$ x(k+1)\leq x(k)\exp \bigl\{ a(k)-b(k)x(k) \bigr\} $$

for \(k\in N\), where \(a(k)\) and \(b(k)\) are non-negative sequences bounded above and below by positive constants. Then

$$ \limsup_{k\to +\infty }x(k)\leq \frac{1}{b^{l}}\exp \bigl(a^{u}-1\bigr). $$

Lemma 2.2

([22])

Assume that \(\{x(k) \}\) satisfies

$$ x(k+1)\geq x(k)\exp \bigl\{ a(k)-b(k)x(k) \bigr\} , k\geq N_{0}, $$

\(\limsup_{k\to +\infty }x(k)\leq x^{*}\) and \(x(N_{0})>0\), where \(a(k)\) and \(b(k)\) are non-negative sequences bounded above and below by positive constants and \(N_{0}\in N\). Then

$$ \liminf_{k\to +\infty }x(k)\geq \min \biggl\{ \frac{a^{l}}{b^{u}}\exp \bigl(a^{l}-b^{u}x^{*}\bigr), \frac{a^{l}}{b^{u}} \biggr\} . $$

3 Permanence

Theorem 3.1

Assume that

$$ m< \min \biggl\{ \frac{r_{1}^{l}p_{1}^{l}-r_{1}^{u}\mu ^{u}M_{2}}{q_{1}^{u}p_{1}^{l}E}, \frac{r_{2}^{l}}{q_{2}^{u}E} \biggr\} .\quad {(H_{1})} $$

Then system (1.3) is permanent.

Proof

From the equations of system (1.3), it follows that

$$ x_{i}(n+1)\leq x_{i}(n)\exp \biggl\{ r_{i}(n)- \frac{r_{i}(n)x_{i}(n)}{p_{i}(n)} \biggr\} , \quad (i=1,2). $$

It follows from Lemma 2.1 that

$$ \limsup_{n\to +\infty }x_{i}(n)\leq \frac{p_{i}^{u}}{r_{i}^{l}}\exp \bigl(r_{i}^{u}-1\bigr)\triangleq M_{i} \quad (i=1,2). $$

So, for small enough \(\varepsilon >0\), there exists \(n_{1}>0\), for all \(n>n_{1}\), we have

$$\begin{aligned}& r_{1}^{l}p_{1}^{l}-r_{1}^{u} \mu ^{u}(M_{2}+\varepsilon )>q_{1}^{u}p _{1}^{l}Em, \\& x_{2}(n)\leq M_{2}+\varepsilon , \qquad r_{2}^{l}-q_{2}^{u}Em>0. \end{aligned}$$

Then, for \(n>n_{1}\), we have

$$ x_{1}(n+1) \geq x_{1}(n)\exp \biggl\{ r_{1}(n)- \frac{r_{1}(n)}{p_{1}(n)}x_{1}(n)- \frac{\mu (n)r_{1}(n)}{p_{1}(n)}(M_{2}+ \varepsilon )-q_{1}^{u}Em \biggr\} . $$

From Lemma 2.2 and letting \(\varepsilon \to 0\), we have

$$ \liminf_{n\to +\infty }x_{1}(n)\geq m_{1}, $$

where

$$\begin{aligned}& m_{1}=\min \biggl\{ \Delta \exp \biggl\{ r_{1}^{l}- \frac{r_{1}^{u}\mu ^{u}M_{2}}{p_{1}^{l}}- q_{1}^{u}Em- \frac{r_{1}^{u}M_{1}}{p_{1}^{l}} \biggr\} , \Delta \biggr\} , \\& \Delta = \frac{r_{1}^{l}p_{1}^{l}-\mu ^{u}r_{1}^{u}M_{2}-p_{1}^{l}q_{1}^{u}Em}{r _{1}^{u}}. \end{aligned}$$

From the second equation of system (1.3) it follows that

$$ x_{2}(n+1)\geq x_{2}(n)\exp \biggl\{ r_{2}^{l}- \frac{r_{2}^{u}}{p_{2}^{l}}x_{2}(n)-q_{2}^{u}Em \biggr\} . $$

From Lemma 2.2 we have

$$ \liminf_{n\to +\infty }x_{2}(n)\geq m_{2}, $$

where

$$ m_{2}=\min \biggl\{ \frac{r_{2}^{l}p_{2}^{l}-p_{2}^{l}q_{2}^{u}Em}{r_{2}^{u}} \exp \biggl\{ r _{2}^{l}-q_{2}^{u}Em- \frac{r_{2}^{u}M_{2}}{p_{2}^{l}} \biggr\} , \frac{r_{2}^{l}p_{2}^{l}-p_{2}^{l}q_{2}^{u}Em}{r_{2}^{u}} \biggr\} . $$

So the proof of Theorem 3.1 is completed. □

4 Extinction

Theorem 4.1

Assume that

$$ m>\max \biggl\{ \frac{r_{1}^{u}}{q_{1}^{l}E}, \frac{r_{2}^{u}}{q_{2}^{l}E} \biggr\} ,\quad {(H_{2})} $$

let \((x_{1}(n), x_{2}(n))^{T}\) be any positive solution of system (1.3), then

$$ \lim_{n\to \infty }x_{i}(n)=0, \quad i=1,2. $$

Proof

From (1.3) we have

$$ x_{i}(n+1)\leq x_{i}(n)\exp \bigl\{ r_{i}^{u}-q_{i}^{l}Em \bigr\} , \quad i=1,2. $$
(4.1)

By using (4.1), we get

$$ \prod_{p=0}^{n-1}x_{i}(p+1)\leq \prod_{p=0}^{n-1}x_{i}(p) \exp \bigl\{ r_{i}^{u}-q_{i}^{l}Em \bigr\} , \quad i=1,2. $$

That is,

$$ x_{i}(n)\leq x_{i}(0)\exp \bigl\{ n \bigl(r_{i}^{u}-q_{i}^{l}Em \bigr) \bigr\} , \quad i=1,2. $$

For \(x_{i}(0)>0\), \(i=1,2\). So it is easy to get that \(x_{i}(n)>0\), \(i=1,2\). Since \((H_{2})\) holds, we have

$$ \lim_{n\to \infty }x_{i}(n)=0, \quad i=1,2. $$

The proof of Theorem 4.1 is completed. □

In this section, we will use the analysis technique of [14].

Theorem 4.2

Assume that

$$ \begin{aligned} &r_{2}^{l}-q_{2}^{u}Em>0, \\ &r_{1}^{u}-q_{1}^{l}Em>0, \\ & \frac{r_{1}^{u}-q_{1}^{l}Em}{r_{2}^{l}-q_{2}^{u}Em}< \frac{r_{1}^{l}\mu ^{l}p_{2}^{l}}{r_{2}^{u}p_{1}^{u}} \end{aligned} \quad {(H_{3})} $$

holds, let \((x_{1}(n),x_{2}(n))^{T}\) be any positive solution of system (1.3), then the species \(x_{2}\) is permanent, while \(x_{1}\) will be driven to extinction.

Proof

By (\(H_{3}\)) we can choose positive constants α and β such that

$$ \frac{r_{1}^{u}-q_{1}^{l}Em}{r_{2}^{l}-q_{2}^{u}Em}< \frac{\beta }{\alpha }< \frac{r_{1}^{l}\mu ^{l}p_{2}^{l}}{r_{2}^{u}p_{1}^{u}}. $$
(4.2)

Thus

$$ \begin{gathered} \alpha \bigl(r_{1}^{u}-q_{1}^{l}Em \bigr)< \beta \bigl(r_{2}^{l}-q_{2}^{u}Em \bigr), \\ \frac{\beta r_{2}^{u}}{p_{2}^{l}}< \frac{\alpha r_{1}^{l}\mu ^{l}}{p_{1}^{u}}, \end{gathered} $$
(4.3)

and there exists \(\delta >0\)

$$ \beta \bigl(r_{2}^{l}-q_{2}^{u}Em\bigr)- \alpha \bigl(r_{1}^{u}-q_{1}^{l}Em \bigr)>\delta >0. $$
(4.4)

Let \((x_{1}(n),x_{2}(n))^{T}\) be any positive solution of system (1.3). For any \(k\in N\), we can get

$$\begin{aligned}& \begin{aligned}[b] \ln \frac{x_{1}(k+1)}{x_{1}(k)} &= r_{1}(k) \biggl(1- \frac{x_{1}(k)}{p_{1}(k)}- \frac{\mu (k)}{p_{1}(k)}x_{2}(k) \biggr)-q_{1}(k)Em \\ &\leq r_{1}^{u}- \frac{r_{1}^{l}}{p_{1}^{u}}x_{1}(k)- \frac{r_{1}^{l}\mu ^{l}}{p_{1}^{u}}x_{2}(k)-q_{1}^{l}Em, \end{aligned} \end{aligned}$$
(4.5)
$$\begin{aligned}& \begin{aligned}[b] \ln \frac{x_{2}(k+1)}{x_{2}(k)} &= r_{2}(k) \biggl(1- \frac{x_{2}(k)}{p_{2}(k)} \biggr)-q_{2}(k)Em \\ &\geq r_{2}^{l}- \frac{r_{2}^{u}}{p_{2}^{l}}x_{2}(k)-q_{2}^{u}Em. \end{aligned} \end{aligned}$$
(4.6)

Then, inequalities (4.3)–(4.6) lead to

$$ \begin{aligned}[b] &\alpha \ln \frac{x_{1}(k+1)}{x_{1}(k)}-\beta \ln \frac{x_{2}(k+1)}{x_{2}(k)} \\ &\quad \leq \alpha \bigl(r_{1}^{u}-q_{1}^{l}Em \bigr)-\alpha \frac{r_{1}^{l}}{p_{1}^{u}}x_{1}(k)-\alpha \frac{ r_{1}^{l}\mu ^{l}}{p_{1}^{u}}x_{2}(k)- \beta \bigl(r_{2}^{l}-q_{2} ^{u}Em\bigr)+ \beta \frac{r_{2}^{u}}{p_{2}^{l}}x_{2}(k) \\ &\quad = \bigl[\alpha \bigl(r_{1}^{u}-q_{1}^{l}Em \bigr)-\beta \bigl(r_{2}^{l}-q_{2}^{u}Em \bigr) \bigr]+ \biggl( \frac{\beta r_{2}^{u}}{p_{2}^{l}}- \frac{\alpha r_{1}^{l}\mu ^{l}}{p_{1}^{u}} \biggr)x_{2}(k)-\alpha \frac{ r_{1}^{l}}{p_{1}^{u}}x_{1}(k) \\ &\quad < -\delta \\ &\quad < 0. \end{aligned} $$
(4.7)

Summating both sides of (4.7) from 0 to \(n-1\), we obtain

$$ \alpha \ln \frac{x_{1}(n)}{x_{1}(0)}-\beta \ln \frac{x_{2}(n)}{x_{2}(0)}< -n\delta . $$
(4.8)

Then

$$ x_{1}(n)< x_{1}(0) \biggl( \frac{x_{2}(n)}{x_{2}(0)} \biggr)^{ \frac{\beta }{\alpha }} \exp \biggl\{ - \frac{n}{\alpha }\delta \biggr\} . $$
(4.9)

Theorem 3.1 implies that \(x_{2}(n)\) is bounded eventually. Then the above inequality (4.9) shows that \(\lim_{n\to \infty }x_{1}(n)=0\). Since \(r_{2}^{l}-q_{2}^{u}Em>0\), then the species \(x_{2}\) is permanent.

The proof of Theorem 4.2 is completed. □

5 Globally attractive

Theorem 5.1

Assume that \(m> \frac{r_{2}^{u}}{q_{2}^{l}E}\) \((H_{4})\) holds and there exists a positive constant \(\eta >0\) such that

$$ \min \biggl\{ \frac{r_{1}^{l}}{p_{1}^{u}}, \frac{2}{M_{1}}- \frac{r_{1}^{u}}{p_{1}^{l}} \biggr\} >\eta \quad (H_{5}) $$

holds, then species \(x_{1}\) is globally attractive while \(x_{2}\) will be driven to extinction.

Proof

Suppose that \((x_{1}(n), x_{2}(n))^{T}\), \((x_{1}^{*}(n), x _{2}^{*}(n))^{T}\) are any two positive solutions of system (1.3). Under the assumption condition \((H_{4})\), it follows from Theorem 4.1 that \(\lim_{n\to +\infty }x_{2}(n)=0\). Since \(\limsup_{n\to \infty }x_{1}(n)< M_{1}\), then for small enough \(\varepsilon >0\), there exists \(N_{0}>0\), for all \(n>N_{0}\), we have

$$ x_{1}(n)< M_{1}+\varepsilon ,\qquad x_{2}(n)< \varepsilon ,\qquad \min \biggl\{ \frac{r_{1}^{l}}{p_{1}^{u}}, \frac{2}{M_{1}+\varepsilon }- \frac{r_{1}^{u}}{p_{1}^{l}} \biggr\} >\eta . $$

To end the proof of Theorem 5.1, it is enough to show that \(\lim_{n\to +\infty }(x_{1}(n)-x_{1}^{*}(n))=0\).

Let \(V(n)=|\ln x_{1}(n)-\ln x_{1}^{*}(n)|\). From (1.3) we have

$$\begin{aligned} \bigl\vert \ln x_{1}(n+1)-\ln x_{1}^{*}(n+1) \bigr\vert =& \biggl\vert \ln x_{1}(n)-\ln x_{1}^{*}(n)- \frac{r_{1}(n)}{p_{1}(n)}\bigl(x_{1}(n)-x_{1}^{*}(n) \bigr) \\ &{}- \frac{\mu (n)r_{1}(n)}{p_{1}(n)}\bigl(x_{2}(n)-x_{2}^{*}(n) \bigr) \biggr\vert \\ \leq & \biggl\vert \ln x_{1}(n)-\ln x_{1}^{*}(n)- \frac{r_{1}(n)}{p_{1}(n)}\bigl(x_{1}(n)-x_{1}^{*}(n) \bigr) \biggr\vert \\ &{}+ \frac{\mu (n)r_{1}(n)}{p_{1}(n)} \bigl\vert x_{2}(n)-x_{2}^{*}(n) \bigr\vert . \end{aligned}$$

Since \(\ln x_{1}(n)-\ln x_{1}^{*}(n)= \frac{1}{\xi _{1}(n)}(x_{1}(n)-x_{1}^{*}(n))\), where \(\min \{x _{1}(n), x_{1}^{*}(n) \}\leq \xi _{1}(n)\leq \max \{x_{1}(n), x _{1}^{*}(n) \}\leq M_{1}+\varepsilon \). So we can get

$$\begin{aligned} \Delta V(n) \leq & - \biggl( \frac{1}{\xi _{1}(n)}- \biggl\vert \frac{1}{\xi _{1}(n)}- \frac{r_{1}(n)}{p_{1}(n)} \biggr\vert \biggr) \bigl\vert x_{1}(n)-x_{1}^{*}(n) \bigr\vert \\ &{}+ \frac{\mu ^{u}r_{1}^{u}}{p_{1}^{l}} \bigl\vert x_{2}(n)-x_{2}^{*}(n) \bigr\vert \\ \leq & -\min \biggl\{ \frac{r_{1}^{l}}{p_{1}^{u}}, \frac{2}{M_{1}+\varepsilon }- \frac{r_{1}^{u}}{p_{1}^{l}} \biggr\} \bigl\vert x_{1}(n)-x_{1}^{*}(n) \bigr\vert +2 \frac{\mu ^{u}r_{1}^{u}}{p_{1}^{l}}\varepsilon \\ \leq &-\eta \bigl\vert x_{1}(n)-x_{1}^{*}(n) \bigr\vert +2 \frac{\mu ^{u}r_{1}^{u}}{p_{1}^{l}}\varepsilon . \end{aligned}$$

Letting \(\varepsilon \to 0\), it follows that

$$ \Delta V(n)\leq -\eta \bigl\vert x_{1}(n)-x_{1}^{*}(n) \bigr\vert , $$

then

$$ \sum_{p=N_{0}}^{n}\bigl(V(p+1)-V(p)\bigr)\leq - \eta \sum_{p=N_{0}} ^{n} \bigl\vert x_{1}(p)-x_{1}^{*}(p) \bigr\vert , $$

that is,

$$ V(n+1)-V(N_{0})\leq -\eta \sum_{p=N_{0}}^{n} \bigl\vert x_{1}(p)-x_{1} ^{*}(p) \bigr\vert , $$

therefore

$$ \sum_{p=N_{0}}^{n} \bigl\vert x_{1}(p)-x_{1}^{*}(p) \bigr\vert \leq \frac{V(N_{0})}{\eta }< +\infty . $$

So it is easy to know that \(\lim_{n\to +\infty }(x_{1}(n)-x _{1}^{*}(n))=0\).

The proof of Theorem 5.1 is completed. □

Similarly, we can get the following theorem.

Theorem 5.2

Assume that there exists a positive constant \(\gamma >0\) such that

$$ \min \biggl\{ \frac{r_{2}^{l}}{p_{2}^{u}}, \frac{2}{M_{2}}- \frac{r_{2}^{u}}{p_{2}^{l}} \biggr\} >\gamma \quad (H_{6}) $$

holds, then the species \(x_{2}\) is globally attractive.

6 Examples and numeric simulations

The following examples lend credence to the plausibility of the main results.

Example 6.1

Corresponding to system (1.3), we assume that

$$ \begin{aligned} & r_{1}(n)=0.05\bigl(\sin ^{2}n+1\bigr),\qquad p_{1}(n)=0.1(\sin n+2), \\ & q_{1}(n)=0.05\bigl(\cos ^{2} n+1\bigr),\qquad r_{2}(n)=0.8\cos ^{2} n+0.2, \\ &p_{2}(n)=0.04(\cos n+1.5),\qquad q_{2}(n)=2(\cos n+1.5), \\ &m=0.1, \qquad \mu (n)=0.05,\qquad E=1. \end{aligned} $$
(6.1)

It is easy to see that \(\frac{r_{2}^{l}}{q_{2}^{u}E}=0.4\), \(M_{2}= \frac{p_{2}^{u}}{r_{2}^{l}}\exp (r_{2}^{u}-1)=0.5\), \(\frac{r_{1}^{l}p_{1}^{l}-r_{1}^{u}\mu ^{u}M_{2}}{q_{1}^{u}p_{1}^{l}E}=0.25\), \(m=0.1<\min \{0.4, 0.25 \}\). Then the conditions of Theorem 3.1 are satisfied (see Fig. 1).

Figure 1
figure 1

Dynamic behaviors of system (6.1) with initial condition \((x_{1}(t),x_{2}(t))^{T}=(0.1, 0.45)^{T},(0.25, 0.25)^{T},(0.35, 0.1)^{T}\)

Example 6.2

Corresponding to system (1.3), we assume that

$$ \begin{aligned} &r_{1}(n)=0.05\bigl(\sin ^{2}n+1 \bigr),\qquad p_{1}(n)=p_{2}(n)=1, \\ &q_{1}(n)=0.05\bigl(\cos ^{2}n+1\bigr),\qquad \mu (n)=0.05, \\ &r_{2}(n)=0.5\cos ^{2} n+0.2,\qquad m=0.8, \\ &q_{2}(n)=0.2(\cos n+1.5),\qquad E=10. \end{aligned} $$
(6.2)

It is easy to see that \(\frac{r_{1}^{u}}{q_{1}^{l}E}=0.2\), \(\frac{r_{2}^{u}}{q_{2}^{l}E}=0.7\), \(m=0.8>\max \{0.2, 0.7 \}\). Then the conditions of Theorem 4.1 are satisfied (see Fig. 2).

Figure 2
figure 2

Dynamic behaviors of system (6.2) with initial condition \((x_{1}(t),x_{2}(t))^{T}=(0.1, 0.3)^{T},(0.25, 0.6)^{T},(0.35, 0.1)^{T}\)

Example 6.3

Corresponding to system (1.3), we assume that

$$ \begin{aligned} &r_{1}(n)=0.05\bigl(\sin ^{2}n+1 \bigr),\qquad p_{1}(n)=0.004(\cos n+1.5), \\ &q_{1}(n)=0.02\bigl(\cos ^{2}n+1\bigr),\qquad r_{2}(n)=0.8\cos ^{2} n+0.3, \\ & q_{2}(n)=0.2(\cos n+1.5),\qquad p_{2}(n)=\sin n+3, \\ & m=0.5, \qquad \mu (n)=1,\qquad E=1. \end{aligned} $$
(6.3)

It is easy to see that \(r_{1}^{u}-q_{1}^{l}Em=0.09>0\), \(r_{2}^{l}-q _{2}^{u}Em=0.05>0\), \(\frac{r_{1}^{u}-q_{1}^{l}Em}{r_{2}^{l}-q_{2}^{u}Em}=1.8< \frac{r_{1}^{l}\mu ^{l}p_{2}^{l}}{r_{2}^{u}p_{1}^{u}}\approx 9.09\). Then the conditions of Theorem 4.2 are satisfied (see Fig. 3).

Figure 3
figure 3

Dynamic behaviors of system (6.3) with initial condition \((x_{1}(t),x_{2}(t))^{T}=(0.1, 0.3)^{T},(0.25, 0.6)^{T},(0.35, 0.1)^{T}\)

Example 6.4

Corresponding to system (1.3), we assume that

$$ \begin{aligned} &r_{1}(n)=p_{1}(n)=p_{2}(n)=1, \qquad q_{1}(n)=0.05\bigl(\cos ^{2}n+1\bigr), \\ &r_{2}(n)=0.5\cos ^{2}n+0.2, \qquad q_{2}(n)=0.2( \cos n+1.5), \\ &\mu (n)=1, \qquad m=0.8,\qquad E=10. \end{aligned} $$
(6.4)

It is easy to see that \(m=0.8> \frac{r_{2}^{u}}{q_{2}^{l}E}=0.7\), \(\min \{ \frac{r_{1}^{l}}{p_{1}^{u}}, \frac{2}{M_{1}}- \frac{r_{1}^{u}}{p_{1}^{l}}=\min \{1,1 \} \}>0\), \(M _{1}= \frac{p_{1}^{u}}{r_{1}^{l}}\exp (r_{1}^{u}-1)=1\). Then the conditions of Theorem 5.1 are satisfied (see Fig. 4).

Figure 4
figure 4

Dynamic behaviors of system (6.4) with initial condition \((x_{1}(t),x_{2}(t))^{T}=(0.1, 0.8)^{T},(0.25, 0.6)^{T},(0.35, 0.3)^{T}\)

7 Discussion

With the aim of the ecological sustainability and conservation of the species to be implemented in a long run, in this paper, we have attempted to study the dynamic behaviors of a non-selective harvesting Lotka–Volterra discrete amensalism model. We have proved that if \((H_{1})\) holds, then the system is permanent, which means that if m, which is the fraction of the stock available for harvesting, is small enough, the system will coexist. Theorem 4.1 implies that if m is large enough, then the system will be driven to extinction. Theorem 4.2 gives some threshold on m, which ensures that the species \(x_{2}\) is permanent while \(x_{1}\) will be driven to extinction. In Sect. 5, sufficient conditions for the global attractivity of (1.3) are given, which means that if m is larger than a certain value and satisfies \((H_{5})\), then the species \(x_{1}\) is globally attractive while \(x_{2}\) will be driven to extinction. The results obtained in this paper maybe useful in designing the natural protection area.

References

  1. Xiong, H.H., Wang, B.B., Zhang, H.L.: Stability analysis on the dynamic model of fish swarm amensalism. Adv. Appl. Math. 5(2), 255–261 (2016)

    Article  Google Scholar 

  2. Han, R.Y., Xue, Y.L., Yang, L.Y., et al.: On the existence of positive periodic solution of a Lotka–Volterra amensalism model. J. Rongyang Univ. 33(2), 22–26 (2015)

    Google Scholar 

  3. Chen, B.G.: Dynamic behaviors of a non-selective harvesting Lotka–Volterra amensalism model incorporating partial closure for the populations. Adv. Differ. Equ. 2018, 111 (2018)

    Article  MathSciNet  Google Scholar 

  4. Sun, G.C.: Qualitative analysis on two populations amensalism model. J. Jiamusi Univ. (Nat. Sci. Ed.) 21(3), 283–286 (2003)

    Google Scholar 

  5. Zhang, Z.P.: Stability and bifurcation analysis for a amensalism system with delays. Math. Numer. Sin. 2, 213–224 (2008)

    Article  MathSciNet  Google Scholar 

  6. Sita Rambabu, B., Narayan, K.L., Bathul, S.: A mathematical study of two species amensalism model with a cover for the first species by homotopy analysis method. Adv. Appl. Sci. Res. 3(3), 1821–1826 (2012)

    Google Scholar 

  7. Chen, F.D., He, W.X., Han, R.Y.: On discrete amensalism model of Lotka–Volterra. J. Beihua Univ. Nat. Sci. 16(2), 141–144 (2015)

    Article  Google Scholar 

  8. Xie, X.D., Chen, F.D., He, M.X.: Dynamic behaviors of two species amensalism model with a cover for the first species. J. Math. Comput. Sci. 16, 395–401 (2016)

    Article  Google Scholar 

  9. Lin, Q.X., Zhou, X.Y.: On the existence of positive periodic solution of a amensalism model with Holling II functional response. Commun. Math. Biol. Neurosci. 2017, Article ID 3 (2017)

    Google Scholar 

  10. Chen, J.H., Wu, R.X.: A two species amensalism model with non-monotonic functional response. Commun. Math. Biol. Neurosci. 2016, Article ID 19 (2016)

    Google Scholar 

  11. Chen, F.D., Zhang, M.S., Han, R.Y.: Existence of positive periodic solution of a discrete Lotka–Volterra amensalism model. J. Shengyang Univ. (Nat. Sci.) 27(3), 251–254 (2015)

    Google Scholar 

  12. Wu, R.X., Zhao, L., Lin, Q.X.: Stability analysis of a two species amensalism model with Holling II functional response and a cover for the first species. J. Nonlinear Funct. Anal. 2016, Article ID 46 (2016)

    Google Scholar 

  13. Chakraborty, K., Das, S., Kar, T.K.: On non-selective harvesting of a multispecies fishery incorporating partial closure for the populations. Appl. Comput. Math. 221, 581–597 (2013)

    MathSciNet  MATH  Google Scholar 

  14. Li, Z., Chen, F.D.: Extinction in two dimensional discrete Lotka–Volterra competitive system with the effect of toxic substances. Dyn. Contin. Discrete Impuls. Syst., Ser. B, Appl. Algorithms 15(2), 165–178 (2008)

    MathSciNet  MATH  Google Scholar 

  15. Chen, X.Y., Shi, C.L.: Permanence and global attractivity of a discrete Nicholson’s blowflies model with delay. J. Math. Res. Appl. 37(2), 233–241 (2017)

    MathSciNet  MATH  Google Scholar 

  16. Li, Y.K., Zhang, T.W.: Almost periodic solution for a discrete hematopoiesis model with time delay. Int. J. Biomath. 5(1), 1–9 (2012)

    MathSciNet  Google Scholar 

  17. Li, Z., Han, M.A., Chen, F.D.: Almost periodic solutions of a discrete almost periodic logistic equation with delay. Appl. Math. Comput. 232(1), 743–751 (2014)

    MathSciNet  MATH  Google Scholar 

  18. Zhou, T.J., Zhang, X.L., Xiang, M.H., Wu, Z.H.: Permanence and almost periodic solution of a predator–prey discrete system with Holling IV functional response. Int. J. Biomath. 2016(3), 39–64 (2016)

    MathSciNet  MATH  Google Scholar 

  19. Li, Z., Chen, F.D.: Almost periodic solutions of a discrete almost periodic logistic equation. Math. Comput. Model. 50(1–2), 254–259 (2009)

    Article  MathSciNet  Google Scholar 

  20. Kar, T.K., Chaudhuri, K.S.: On non-selective harvesting of two competing fish species in the presence of toxicity. Ecol. Model. 161(1–2), 125–137 (2003)

    Article  Google Scholar 

  21. Chen, F.D.: Permanence and global attractivity of a discrete multi-species Lotka–Volterra competition predator–prey systems. Appl. Math. Comput. 182(1), 3–12 (2006)

    MathSciNet  MATH  Google Scholar 

  22. Chen, F.D.: Permanence for the discrete mutualism model with time delays. Math. Comput. Model. 47(3–4), 431–435 (2008)

    Article  MathSciNet  Google Scholar 

Download references

Acknowledgements

Not applicable.

Availability of data and materials

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

Funding

This work is supported by the Natural Science Project of Fujian province (2015 J 01012, 2015 J 01019) and the Funding of the Young Key Teachers Training Program of Zhengzhou Chenggong University of Finance and Economics.

Author information

Authors and Affiliations

Authors

Contributions

QQS is a major contributor in writing the manuscript. FDC is responsible for numerical simulation and drawing. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Qianqian Su.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

We agree to publish in your journal.

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 distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Su, Q., Chen, F. The influence of partial closure for the populations to a non-selective harvesting Lotka–Volterra discrete amensalism model. Adv Differ Equ 2019, 281 (2019). https://doi.org/10.1186/s13662-019-2209-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13662-019-2209-y

Keywords