Abstract and Applied Analysis

Volume 2014 (2014), Article ID 928726, 6 pages

http://dx.doi.org/10.1155/2014/928726

Research Article

Global Attractivity of an Integrodifferential Model of Mutualism

Xiangdong Xie,¹ Fengde Chen,¹ Kun Yang,² and Yalong Xue²

¹Department of Mathematics, Ningde Normal University, Fujian 352100, China

²College of Mathematics and Computer Science, Fuzhou University, Fuzhou, Fujian 350116, China

Received 12 January 2014; Revised 8 March 2014; Accepted 9 March 2014; Published 1 April 2014

Academic Editor: Yongli Song

Copyright © 2014 Xiangdong Xie et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Sufficient conditions are obtained for the global attractivity of the following integrodifferential model of mutualism: , , where and , , are all positive constants. Consider , Consider and , Our result shows that conditions which ensure the permanence of the system are enough to ensure the global stability of the system. The result not only improves but also complements some existing ones.

1. Introduction

Mutualism, one of the most important relationships in the theory of ecology, however, was pointed out by Murray as follows [1]: “this area has not been as widely sutdied as the others even though its importance is comparable to that of predator-prey and competition interactions.”

Traditional two species Lotka-Volterra take the form

Murray [1] gave detail analysis of the phase trajectories for the above system. He also pointed out that the system has certain drawback; one is the sensitivity between unbounded growth and a finite positive steady state. Despite the drawback of the system, since it is the most simple model on the mutualism, scholars incorporated delays to the above system and proposed the following system:

Chen et al. [2] had given two examples to show that under the assumption , a condition which could ensure the global stability of the system without delay, the system still admits unbounded solution. He and Gopalsamy [3] and Mukherjee [4] tried to investigate the persistent and stability property of the nonautonomous case of above system; however, in their main results, in addition to condition , they further assumed that the density of one of the species should be bounded from above, such an assumption is by no means easy to verify. To overcome this difficulty, Lu et al. [5, 6] and Nakata and Muroya [7] tried to give restriction on the coefficients of the system or restriction on the delay of the system, and some interesting results about the permanence of Lotka-Volterra type mutualism system with delay were obtained. Liu et al. [8] and Lu [9] also investigated the positive periodic solution of the Lotka-Volterra type mutualism model.

On the other hand, stimulated by the functional response of the predator-prey system, Wright [10] proposed the following two species mutualism model:

Obviously, the model could be revised as follows:

where , , and one could easily see that , .

It is well known that in a more realistic model the delay effect should be an average over past populations. This results in an equation with a distributed delay or an infinite delay. Based on the model (4), Gopalsamy [11] further proposed the following two species mutualism model:

However, the author did not investigate the dynamic behaviors of the system.

Recently, Li and Xu [12] proposed and studied the following nonautonomous case of the system (5):

where , , , and , , are continuous functions bounded above and below by positive constants. Consider , . Consider and , . Under the assumption that , , and , , are continuous periodic functions with common period . , , and , . By applying the coincidence degree theory, they showed that system (6) admits at least one positive -periodic solution. Chen and You [13] argued that the general nonautonomous case is more suitable. Concerned with the persistent property of the system (6), by applying an integral inequality (see Lemma 3 in the next section), they obtained the following result.

Theorem A. The system (6) is always permanent. That is, there exist constants , , , which are independent of the solution of the system (6), such that

Such a result is a roughly one, since it only tells us that the solution is finally bounded above and below by positive constants and there is no fine description of the stable or unstable property of the solution, for example, whether the delay of the system could induce the Hopf bifurcation to period solution or not? Does the system admit some kind of chaotic behaviors? Is it difficult to obtain sufficient conditions which ensure the global attractivity of the positive solution? Indeed, to the best of the authors’ knowledge, to this day, still no scholars investigate the stability property of the system (6), which is one of the most important topics in the study of population dynamics. Noting that system (6) is nonautonomous one and for such kind of system, generally speaking, by constructing some suitable Lyapunov functional, one could always obtain some sufficient conditions which ensure the stability of the system; however, the condition is not easy to verify [14]. This motivated us to investigate the stability property of the system (5).

From the point of view of biology, in the sequel, we will consider (5) together with the initial conditions

where and

From [15], system (5) has a unique positive solution satisfying the initial condition (8).

The aim of this paper is, by further developing the analysis technique of Chen and You [13] and de Oca and Vivas [16] and using the differential inequality theory, to obtain a set of sufficient conditions to ensure the global attractivity of the system (5). More precisely, we will prove the following result.

Theorem 1. System (5) admits a unique positive equilibrium , which is globally attractive; that is, for any positive solution of system (5) with the initial condition (8), one has

We will prove this theorem in the next section and then give a brief discussion in Section 3. For more works on the mutualism or cooperation system, one could refer to [12–15, 17–21] and the references cited therein.

2. Proof of the Main Result

Now let us state several lemmas which will be useful in the proving of main result.

Lemma 2. System (5) admits a unique positive equilibrium .

Proof. The positive equilibrium of the system (5) satisfies the following equation:

System (11) admits a unique positive solution , where

This ends the proof of Lemma 2.

Following Lemma 3 is Lemma 3 of de Oca and Vivas [16].

Lemma 3. Let be a bounded nonnegative continuous function, and let be a continuous kernel such that . Then

As a direct corollary of Lemma 2.2 of Chen [22], we have the following lemma.

Lemma 4. If , , and , when and , one has

If , and , when and , one has

Now we are in the position of proving the main result of this paper.

Proof of Theorem 1. Let be any positive solution of the system (5) with initial condition (8). Similarly to the analysis of (11)–(17) in [13], from the first equation of the system (5) it follows that

Thus, as a direct corollary of Lemma 4, according to (16), one has

and so, from Lemma 3 we have

Hence, for enough small , it follows from (17) and (18) that there exists a such that

Similarly, for above , it follows from the second equation of the system (5) that there exists a such that

Noting that the function is a strictly increasing function, hence, (20) together with the first equation of the system (5) implies

Therefore, by Lemma 4, we have

Thus, from Lemma 3 we have

That is, for defined by (19), there exists a such that

Similarly to the analysis of (22)–(24), from (19) and the second equation of the system (5), there exists a such that

Since the function is a strictly increasing function, one could easily see that , and so, from the first equation of the system (5), it follows that

Thus, as a direct corollary of Lemma 4, according to (25), one has

and so, from Lemma 3, we have

Hence, for enough small , it follows from (27) and (28) that there exists a such that

Similarly, for above , it follows from the second equation of the system (5) that there exists a such that

Noting that the function is a strictly increasing function, hence, (30) together with the first equation of the system (5) implies

Therefore, by Lemma 4, we have

Thus, from Lemma 3 we have

That is, there exists a such that

Similarly to the analysis of (32)–(34), from (28) and the second equation of the system (5), there exists a such that

One could easily see that

Repeating the above procedure, we get four sequences , , , , such that for

Obviously,

We claim that sequences , are nonincreasing and sequences , are nondecreasing. To prove this claim, we will carry out by induction. Firstly, from (36) we have

Let us assume now that our claim is true for ; that is,

Again from the strict increasing of the function , we immediately obtain

Therefore,

Letting in (37), we obtain

and (43) shows that and are solutions of (11). By Lemma 2, (11) has a unique positive solution . Hence, we conclude that

that is,

Thus, the unique interior equilibrium is globally attractive. This completes the proof of Theorem 1.

3. Discussion

As was pointed out in the introduction section, for Lotka-Volterra type mutualism system, conditions which ensure the globally stability of the system are not so easily verified [3, 4]. In this paper, we study the stability property of the integrodifferential model of mutualism (5). By applying the iterative technique, we obtain a set of sufficient conditions which guarantee the global attractivity of the coexistence equilibrium. Our result (Theorem 1) shows that the conditions which ensure the permanence of the system are enough to ensure the global attractivity of the system. The new finding of this paper is that we found the iterative bound of the solution, such a finding is not detected by Chen and You [13]. Based on this finding, it is possible to obtain the subtle result about the stability of the system. We mention here that we did not consider the delay in the intraspecific competition; whether such kind of delay could induce bifurcation or not is still unknown; we leave this for future study.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors are grateful to anonymous referees for their excellent suggestions, which greatly improved the presentation of the paper. Also, this work was supported by the Natural Science Foundation of Fujian Province (2013J01011 and 2013J01010) and the Foundation of Fujian Education Bureau (JA13361).

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