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# Extinction for a discrete competition system with the effect of toxic substances

*Advances in Difference Equations*
**volumeÂ 2016**, ArticleÂ number:Â 1 (2016)

## Abstract

A nonautonomous discrete competitive system with nonlinear inter-inhibition terms and one toxin producing species is studied in this paper. Sufficient conditions which guarantee the extinction of one of the components are obtained and the global attractivity of the other one is proved. Our results supplement some existing ones. Numerical simulations show the feasibility of our results.

## 1 Introduction

For any bounded sequence \(\{f(n)\}\), \(f^{L}=\inf_{n\in N} \{f(n)\}\), \(f^{M}=\sup_{n\in N} \{f(n)\}\).

Recently, many authors considered the following discrete two species competitive system with nonlinear inter-inhibition terms (see [1â€“4]):

where \(r_{i}(n)\), \(a_{i}(n)\), \(c_{i}(n)\) (\(i=1,2\)) are assumed to be bounded positive sequences and \(x_{1}(n)\), \(x_{2}(n)\) are population density of species \(x_{1}\) and \(x_{2}\) at the *n*th generation, respectively. For the ecological meaning of model (1.1), see [1]. Sufficient conditions which guarantee the permanence, existence, and global stability of positive periodic solutions of system (1.1) were established by Qin *et al.* [1]. By using the Lyapunov function, some analysis techniques, and preliminary lemmas, Wang and Liu [2] further established a criterion for the existence, uniqueness, and uniformly asymptotic stability of positive almost periodic solution of system (1.1) with almost periodic parameters. Noting that ecosystems in the real world are often distributed by unpredictable forces which can result in changes in biological parameters, Wang *et al.* [3] investigated the existence and uniformly asymptotic stability of the unique positive almost periodic solution of system (1.1) with almost periodic parameters and feedback controls. Yu [4] further showed that feedback control variables have no influence on the persistent property of the system. On the other hand, as we all know, the extinction property is also an important topic in the study of mathematical biology; however, until now there are still no scholar investigations of this property of system (1.1). One aim of this work is to obtain a set of sufficient conditions which guarantee the extinction of system (1.1).

In recent years, the competition system with toxic substance has been widely studied. Li and Chen [5] studied the extinction property and global attractivity of the following two species discrete competitive system:

SolÃ© *et al.* [6] and Bandyopadhyay [7] considered the Lotka-Volterra system of two interacting phytoplankton species with one species that could be toxic, while the other one is non-toxic. The stability property of the equilibrium of the system is obtained. Motivated by the above ideas, Chen *et al.* [8] introduced the following system:

where \(x_{1}(n)\) represents the density of non-toxic phytoplankton and \(x_{2}(n)\) is the toxic liberating phytoplankton. The coefficients in system (1.3) have the same restriction as that in system (1.2) and system (1.3) is a special case of (1.2) with \(b_{2}(n)\equiv0\), *i.e.*, the first species could not be toxic. They obtain several sets of sufficient conditions which guarantee the extinction of the one species and the global stability of the other species. To the best of the authorâ€™s knowledge, to this day, no work has been done previously on the discrete competitive system with nonlinear inter-inhibition terms and one toxin producing species. Hence, we consider the following system:

where all the coefficients have the same meaning as that of systems (1.1)-(1.3), and for \(i, j = 1, 2\), \({r_{i}(n)}\), \({a_{ij}(n)}\), and \({b_{1}(n)}\) are bounded nonnegative sequences defined for \(n\in N = \{0, 1, 2, \ldots\}\) such that

As regards the biological meaning, we assume (1.4) together with the initial conditions: \(x_{1}(0) > 0\) and \(x_{2}(0) > 0\). It is not difficult to see that the solutions of (1.4) are defined and remain positive for all \(n\in N\). For more relevant work, one could refer to [5â€“19] and the references cited therein.

The remaining part of this paper is organized as follows. In SectionÂ 2, we study the extinction of some one species. The global stability of the other species when the previous species is eventually in extinction both for systems (1.4) and (1.1) is then studied in SectionÂ 3. Some examples together with their numerical simulations are presented in SectionÂ 4 to show the feasibility of our results. We give a brief discussion in the last section.

## 2 Extinction

In this section, we will establish sufficient conditions on the extinction of species \(x_{2}\) or \(x_{1}\). By a similar proof to LemmaÂ 2.1 in Li and Chen [5], we can obtain the following result.

### Lemma 2.1

*Any positive solution*
\((x_{1}(n), x_{2}(n))^{T}\)
*of system* (1.4) *satisfies*

*where*
\(B_{i}=\frac{\exp(r_{i}^{M}-1)}{a_{ii}^{L}}\), \(i=1,2\).

LemmaÂ 2.1 shows that the positive solutions of system (1.4) are bounded eventually. We now come to the study of the extinction of species \(x_{2}\) of system (1.4).

### Theorem 2.1

*Assume*

*and*

*hold*, *where*
\(B_{i} \) (\(i = 1, 2\)) *is defined in LemmaÂ *
2.1, *then the species*
\(x_{2}\)
*will be driven to extinction*, *that is*, *for any positive solution*
\((x_{1}(n), x_{2}(n))^{T}\)
*of system* (1.4), \(\lim_{n\rightarrow+\infty}x_{2}(n)=0\).

### Proof

Conditions (H_{1}) and (H_{2}) can be rewritten as

According to (2.2), one can choose a small enough positive constant \(\varepsilon_{1}\) such that

By (2.3), there exist positive constants *Î±* and *Î²* such that

Thus,

and we can choose a constant \(\delta_{1}> 0\), such that

For the above \(\varepsilon_{1}\), it follows from LemmaÂ 2.1 that there exists a large enough *N* such that

For any \(p>N\), according to the equations of system (1.4) and (2.7), we can get

Therefore, inequalities (2.5)-(2.8) show that

Summing both sides of the above inequalities from \(N+1\) to \(n-1\) leads to

hence

The above inequality together with the ultimate boundedness of \(x_{1}(n)\) shows that \(\lim_{n\rightarrow+\infty}x_{2}(n)=0\). The proof is completed.â€ƒâ–¡

### Theorem 2.2

*In addition to* (H_{1}), *further suppose that*

*holds*, *where*
\(B_{i}\) (\(i = 1, 2\)) *is defined in LemmaÂ *
2.1, *then for any positive solution*
\((x_{1}(n), x_{2}(n))^{T}\)
*of system* (1.4), \(\lim_{n\rightarrow+\infty}x_{2}(n)=0\).

### Proof

It follows from conditions (H_{1}) and (H_{3}) that

Thus, one can choose a small enough positive constant \(\varepsilon_{2}\) such that

By (2.13), there exist positive constants *Î±* and *Î²* such that

So

and we can choose a constant \(\delta_{2}> 0\), such that

Therefore, inequalities (2.15), (2.16), (2.7), and (2.8) show that

The rest of the proof is similar to that of the corresponding proof of TheoremÂ 2.1, we omit the details here. This ends the proof of TheoremÂ 2.2.â€ƒâ–¡

### Theorem 2.3

*Let*
\((x_{1}(n), x_{2}(n))^{T}\)
*be any positive solution of system* (1.4), *in addition to* (H_{1}), *further suppose that*

*holds*, *where*
\(B_{1}\)
*is defined in LemmaÂ *
2.1, *then*
\(\lim_{n\rightarrow+\infty}x_{2}(n)=0\).

### Proof

It follows from conditions (H_{1}) and (H_{4}) that

Thus, one can choose a small enough positive constant \(\varepsilon_{3}\) such that

By (2.19), there exist positive constants *Î±* and *Î²* such that

Thus,

and we can choose a constant \(\delta_{3}> 0\), such that

Therefore, inequalities (2.21), (2.22), (2.7), and (2.8) show that

The rest of the proof is similar to that of the corresponding proof of TheoremÂ 2.1, we omit the details here. This ends the proof of TheoremÂ 2.3.â€ƒâ–¡

Now, let us investigate the extinction property of species \(x_{1}\) in system (1.4) which is also an interesting problem and we obtain the following result.

### Theorem 2.4

*Let*
\((x_{1}(n), x_{2}(n))^{T}\)
*be any positive solution of system* (1.4). *Suppose*

*holds*, *where*
\(B_{2}\)
*is defined in LemmaÂ *
2.1, *then the species*
\(x_{1}\)
*will be driven to extinction*, *that is*, \(\lim_{n\rightarrow+\infty}x_{1}(n)=0\).

### Proof

According to (H_{5}), one can choose a small enough positive constant \(\varepsilon_{4}\) such that

By (2.24), there exist positive constants *Î±* and *Î²* such that

Thus,

and we can choose a constant \(\delta_{4}> 0\), such that

For any \(p>N\), according to the equations of system (1.4) and (2.7), we can get

Therefore, inequalities (2.26)-(2.28) show that

The rest of the proof is similar to that of the corresponding proof of TheoremÂ 2.1, we omit the details here. This ends the proof of TheoremÂ 2.4.â€ƒâ–¡

## 3 Global stability

In SectionÂ 2, we get sufficient conditions which guarantee the extinction of the first or second species in system which motives us to investigate the stability property of the rest species. Let us first state several lemmas which will be useful in the proof of the main result of this section.

### Lemma 3.1

(see [20])

*Assume that*
\(\{x(n)\}\)
*satisfies*

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

### Lemma 3.2

*Suppose conditions in TheoremÂ *
2.1
*or*
2.2, *or*
2.3
*hold*, *let*
\((x_{1}(n), x_{2}(n))^{T}\)
*be any positive solution of system* (1.4), *then*

*where*
\(A_{1}=\frac{r_{1}^{L}}{a_{11}^{M}}\exp\{r_{1}^{L}-a_{11}^{M}B_{1}\}\)
*and*
\(B_{1}\)
*is defined in LemmaÂ *
2.1.

### Proof

It follows from LemmaÂ 2.1 and TheoremÂ 2.1 or 2.2, or 2.3 that

To end the proof of LemmaÂ 3.2, it is enough to show that

Since \(r_{1}^{L}>0\), there exists a small enough \(\varepsilon>0\) such that

According to (3.1), for the above \(\varepsilon>0\), there exists a large enough \(N_{1}>0\), such that, for \(n\ge N_{1}\),

Thus, it follows from (3.4) and the first equation of system (1.4) that

Since \(A_{\varepsilon}>0\), by applying LemmaÂ 3.1 to (3.5), it immediately follows that

Setting \(\varepsilon\rightarrow0\) in the above inequality, one can obtain

By calculation, one can easily get

Inequality (3.6) together with (3.7) leads to

that is to say, (3.2) holds. This ends the proof of LemmaÂ 3.2.â€ƒâ–¡

### Lemma 3.3

*Suppose conditions in TheoremÂ *
2.4
*hold*, *let*
\((x_{1}(n), x_{2}(n))^{T}\)
*be any positive solution of system* (1.4), *then*

*where*
\(A_{2}=\frac{r_{2}^{L}}{a_{22}^{M}}\exp\{r_{2}^{L}-a_{22}^{M}B_{2}\}\)
*and*
\(B_{2}\)
*is defined in LemmaÂ *
2.1.

### Proof

The proof of LemmaÂ 3.3 is similar to that of the proof of LemmaÂ 3.2, we omit the details here.â€ƒâ–¡

Consider the following discrete logistic equation:

where \(r_{1}(n)\) and \(a_{11}(n)\) are bounded nonnegative sequences.

### Lemma 3.4

(see [8])

*For any positive solution*
\(x(n)\)
*of* (3.9), *we have*

*where*
\(A_{1}\), \(B_{1}\)
*are defined by LemmaÂ *
3.2.

Consider the following discrete logistic equation:

where \(r_{2}(n)\) and \(a_{22}(n)\) are bounded nonnegative sequences.

### Lemma 3.5

(see [8])

*For any positive solution*
\(\tilde{x}(n)\)
*of* (3.10), *we have*

*where*
\(A_{2}\), \(B_{2}\)
*are defined by LemmaÂ *
3.3.

Now, we come to showing the main results of this section.

### Theorem 3.1

*Suppose in addition the conditions of TheoremÂ *
2.1
*or*
2.2, *or*
2.3
*hold*, *further suppose that*

*Then for any positive solution*
\((x_{1}(n), x_{2}(n))^{T}\)
*of system* (1.4), *we have*

*where*
\(x(n)\)
*is any positive solution of system* (3.9).

### Proof

It follows from TheoremÂ 2.1 or 2.2, or 2.3 that

Set \(y(n)=\ln x_{1}(n)-\ln x(n)\), then it follows from the first equation of system (1.4) and (3.9) that

Using the mean value theorem, we can obtain

Substituting (3.13) into the right side of equation (3.12), we can get

Considering (H_{6}) implies that \(-1<1-a_{11}^{M}B_{1}\), there exists a small enough \(\varepsilon>0\) such that

According to LemmaÂ 3.2, LemmaÂ 3.4, and (3.11), for the above \(\varepsilon>0\), there exists large enough \(N>0\), such that, for \(n\ge N\),

Note that \(\theta(n)\in(0,1)\) implies that \(x(n)\exp(\theta (n)y(n))\) lies between \(x(n)\) and \(x_{1}(n)\). From (3.14) and (3.16), for \(n\ge N\), one can get

where \(\lambda_{\varepsilon}=\max \{|1-a_{11}^{M}(B_{1}+\varepsilon )|,|1-a_{11}^{L}(A_{1}-\varepsilon)| \}\), \(M_{\varepsilon}=a_{12}^{M}+b_{1}^{M}(B_{1}+\varepsilon)\). This implies that

Note that \(1-a_{11}^{M}(B_{1}+\varepsilon)\le1-a_{11}^{L}(A_{1}-\varepsilon )<1\), hence \(0<\lambda_{\varepsilon}<1\) according to (3.15). Thus, \(\lim_{n\rightarrow+\infty}y(n)=0\) can be immediately obtained by (3.18), and so \(\lim_{n\rightarrow+\infty }(x_{1}(n)-x(n))=0\). This ends the proof of TheoremÂ 3.1.â€ƒâ–¡

Similarly, by using Lemmas 3.3 and 3.5, we have the following theorem.

### Theorem 3.2

*In addition to the conditions of TheoremÂ *
2.4, *further suppose that*

*Then for any positive solution*
\((x_{1}(n), x_{2}(n))^{T}\)
*of system* (1.4) *and any positive solution*
\(\tilde{x}(n)\)
*of system* (3.10), *we have*

As a direct corollary of TheoremÂ 3.1 and TheoremÂ 3.2, we have the following corollary.

### Corollary 3.1

*In addition to* (H_{1}), *further suppose that*

*Then for any positive solution*
\((x_{1}(n), x_{2}(n))^{T}\)
*of system* (1.1) *and any positive solution*
\(x(n)\)
*of system* (3.9), *we have*

*That is to say*, *the species*
\(x_{2}\)
*will be driven to extinction*.

### Corollary 3.2

*Assume that the conditions of TheoremÂ *
2.4
*hold*, *also*

*Then for any positive solution*
\((x_{1}(n), x_{2}(n))^{T}\)
*of system* (1.1) *and any positive solution*
\(\tilde{x}(n)\)
*of system* (3.10), *we have*

*That is to say*, *the species*
\(x_{1}\)
*will be driven to extinction*.

## 4 Examples and numeric simulation

In this section, we give the following two examples to verify the feasibilities of our results.

### Example 4.1

Consider the following system:

*Case* 1. \(b_{1}(n)=0.2\).

Take easy calculation, we have \(\frac{r_{2}^{M}}{r_{1}^{L}}=0.5\), \(B_{1}\approx0.8143\), \(B_{2}\approx0.5156\), \(\frac {a_{21}^{L}}{a_{11}^{M}(1+B_{1})}\approx1.1024\), \(\frac{a_{22}^{L}}{a_{12}^{M}}=1\), \(r_{1}^{L}-r_{2}^{M}\frac{a_{11}^{M}(1+B_{1})}{a_{21}^{L}}\approx0.6476\), \(r_{1}^{L}-r_{2}^{M}\frac{a_{12}^{M}}{a_{22}^{L}}=0.6\), thus

and

(4.2)-(4.3) show that the coefficients of the system (4.1) satisfy the conditions of TheoremsÂ 2.1, 2.2, and 2.3. Moreover,

Hence, condition (H_{6}) is also satisfied. It follows from TheoremÂ 3.1 that, for any positive solution \((x_{1}(n), x_{2}(n))^{T}\) of system (4.1), we have \(\lim_{n\rightarrow+\infty}(x_{1}(n)-x(n))=0\), \(\lim_{n\rightarrow +\infty}x_{2}(n)=0\), where \(\{x(n)\}\) is any positive solution of the system

Our numerical simulation supports our result (see FigureÂ 1).

*Case* 2. \(b_{1}(n)=0\).

\(b_{1}(n)=0\) shows that the two species are all non-toxic. One can easily find that the conditions in CorollaryÂ 3.1 are satisfied, so for any positive solution \((x_{1}(n), x_{2}(n))^{T}\) of system (4.1) with \(b_{1}(n)=0\), \(x_{2}(n)\) is in extinction while \(x_{1}(n)\) will be globally attractive (see FigureÂ 2).

### Example 4.2

Consider the following system:

*Case* 1. \(b_{1}(n)=0.3\).

In this case, one could easily see that \(\frac{r_{2}^{L}}{r_{1}^{M}}=4\), \(B_{2}\approx0.9395\), \(\frac{a_{21}^{M}}{a_{11}^{L}}=2\), \(\frac {a_{22}^{M}(1+B_{2})}{a_{12}^{L}}\approx1.2607\), so

and

(4.5) and (4.6) mean that all conditions of TheoremÂ 3.2 are satisfied in system (4.4). Thus, for any positive solution \((x_{1}(n), x_{2}(n))^{T}\) of system (4.4) and any positive solution \(\{\tilde{x}(n)\}\) of system (3.10), we have \(\lim_{n\rightarrow+\infty}x_{1}(n)=0\), \(\lim_{n\rightarrow+\infty }(x_{2}(n)-\tilde{x}(n))=0\), where \(\{\tilde{x}(n)\}\) is any positive solution of the system

FigureÂ 3 shows the dynamical behavior of system (4.4) with \(b_{1}(n)=0.3\).

*Case* 2. \(b_{1}(n)=0\).

\(b_{1}(n)=0\) shows that the two species are all non-toxic. One can easily find that the conditions in CorollaryÂ 3.2 are satisfied, so for any positive solution \((x_{1}(n), x_{2}(n))^{T}\) of system (4.4) with \(b_{1}(n)=0\), \(x_{1}(n)\) is in extinction while \(x_{2}(n)\) will be globally attractive (see FigureÂ 4).

## 5 Discussion

In this paper, we consider a two species nonautonomous discrete competitive system with nonlinear inter-inhibition terms and one toxin producing species, *i.e.*, (1.4). By developing the analysis technique of Chen *et al.* [8], sufficient conditions which guarantee the extinction of one of the two species are obtained and the stability property of the other species are proved. As direct results of TheoremÂ 3.1 and TheoremÂ 3.2, Corollaries 3.1 and 3.2 show the same conclusions for a non-toxic system, which supplements the results of [1, 2]. Moreover, by comparing TheoremÂ 3.1 with CorollaryÂ 3.1, and TheoremÂ 3.2 with CorollaryÂ 3.2, we also found that, for such a kind of system, a lower rate of toxic production has no influence on the extinction property of the system.

## References

Qin, W, Liu, Z, Chen, Y: Permanence and global stability of positive periodic solutions of a discrete competitive system. Discrete Dyn. Nat. Soc.

**2009**, Article ID 830537 (2009)Wang, Q, Liu, Z: Uniformly asymptotic stability of positive almost periodic solutions for a discrete competitive system. J. Appl. Math.

**2013**, Article ID 182158 (2013)Wang, Q, Liu, Z, Li, Z: Positive almost periodic solutions for a discrete competitive system subject to feedback controls. J. Appl. Math.

**2013**, Article ID 429163 (2013)Yu, S: Permanence for a discrete competitive system with feedback controls. Commun. Math. Biol. Neurosci.

**2015**, Article ID 16 (2015)Li, Z, Chen, F: 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**, 165-178 (2008)SolÃ©, J, Garca-Ladona, E, Ruardij, P, Estrada, M: Modelling allelopathy among marine algae. Ecol. Model.

**183**, 373-384 (2005)Bandyopadhyay, M: Dynamical analysis of a allelopathic phytoplankton model. J. Biol. Syst.

**14**, 205-217 (2006)Chen, F, Gong, X, Chen, W: Extinction in two dimensional discrete Lotka-Volterra competitive system with the effect of toxic substances (II). Dyn. Contin. Discrete Impuls. Syst., Ser. B, Appl. Algorithms

**20**, 449-461 (2013)Chattopadhyay, J: Effect of toxic substances on a two-species competitive system. Ecol. Model.

**84**, 287-289 (1996)Mukhopadhyay, A, Chattopadhyay, J, Tapaswi, PK: A delay differential equations model of plankton allelopathy. Math. Biosci.

**149**, 167-189 (1998)Li, Z, Chen, F: Extinction in two dimensional nonautonomous Lotka-Volterra systems with the effect of toxic substances. Appl. Math. Comput.

**182**, 684-690 (2006)Chen, F, Li, Z, Chen, X, Laitochov, J: Dynamic behaviors of a delay differential equation model of plankton allelopathy. J. Comput. Appl. Math.

**206**, 733-754 (2007)Liu, Z, Chen, L: Positive periodic solution of a general discrete nonautonomous difference system of plankton allelopathy with delays. J. Comput. Appl. Math.

**197**, 446-456 (2006)Liu, Z, Chen, L: Periodic solution of a two-species competitive system with toxicant and birth pulse. Chaos Solitons Fractals

**32**, 1703-1712 (2007)Liu, Z, Wu, J, Chen, Y, Haque, M: Impulsive perturbations in a periodic delay differential equation model of plankton allelopathy. Nonlinear Anal., Real World Appl.

**11**, 432-445 (2010)Tian, C, Lin, Z: Asymptotic behavior of solutions of a periodic diffusion system of plankton allelopathy. Nonlinear Anal., Real World Appl.

**11**, 1581-1588 (2010)Li, Z, Chen, F, He, M: Asymptotic behavior of the reaction-diffusion model of plankton allelopathy with nonlocal delays. Nonlinear Anal., Real World Appl.

**12**, 1748-1758 (2011)Li, Z, Chen, F, He, M: Global stability of a delay differential equations model of plankton allelopathy. Appl. Math. Comput.

**218**, 7155-7163 (2012)Chen, L, Chen, F: Extinction in a discrete Lotka-Volterra competitive system with the effect of toxic substances and feedback controls. Int. J. Biomath.

**8**, 1550012 (2015)Chen, F: Permanence for the discrete mutualism model with time delays. Math. Comput. Model.

**47**, 431-435 (2008)

## Acknowledgements

The author would like to thank the anonymous referees and the editor for their constructive suggestions on improving the presentation of the paper. Also, this research was supported by Anhui Province College Excellent Young Talents Support Plan Key Projects (No.Â gxyqZD2016240).

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Yue, Q. Extinction for a discrete competition system with the effect of toxic substances.
*Adv Differ Equ* **2016**, 1 (2016). https://doi.org/10.1186/s13662-015-0739-5

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DOI: https://doi.org/10.1186/s13662-015-0739-5