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Dynamical behavior of a pest management model with impulsive effect and nonlinear incidence rate

Abstract

In this paper, we consider the pest management model with spraying microbial pesticide and releasing the infected pests, and the infected pests have the function similar to the microbial pesticide and can infect the healthy pests, further weaken or disable their prey function till death. By using the Floquet theory for impulsive differential equations, we show that there exists a globally asymptotically stable pest eradication periodic solution when the impulsive period τ < τmax, we further prove that the system is uniformly permanent if the impulsive period τ > τmax. Finally, by means of numerical simulation, we showthatwith the increaseof impulsive period, the system displays complicated behaviors.

pest-management model; impulsive effect; extinction; permanence


Dynamical behavior of a pest management model with impulsive effect and nonlinear incidence rate* * Supported by the National Natural Science Foundation of China (No. 10771179), the Natural Science Foundation of the Education Department of Henan Province (No. 2010B110019), the Youth Science Foundation of Xinyang Normal University (20100070), the Young Backbone Teacher Foundation of Xinyang Normal University.

Xia WangI; Zhen GuoII; Xinyu SongI

ICollege of Mathematics and Information Sciences, Xinyang Normal University, Xinyang 464000, Henan, P.R. China E-mail: xywangxia@163.com

IISchool of Computer and Information Technology, Xinyang 464000, Henan, P.R. China

ABSTRACT

In this paper, we consider the pest management model with spraying microbial pesticide and releasing the infected pests, and the infected pests have the function similar to the microbial pesticide and can infect the healthy pests, further weaken or disable their prey function till death. By using the Floquet theory for impulsive differential equations, we show that there exists a globally asymptotically stable pest eradication periodic solution when the impulsive period τ < τmax, we further prove that the system is uniformly permanent if the impulsive period τ > τmax. Finally, by means of numerical simulation, we showthatwith the increaseof impulsive period, the system displays complicated behaviors.

Mathematical subject classification: 34C05, 92D25.

Key words: pest-management model, impulsive effect, extinction, permanence.

1 Introduction

From the reports of Food and Agriculture Organization of the United Nations, the warfare between man and pests has lasted for thousands of years. With the development of society and progress of science and technology, there are many ways to control agricultural pests, for instance biological pesticides, chemical pesticides, remote sensing and measuring and so on. A great deal of pesticides were used to control pests. Generally speaking, pesticides are useful because they can quickly kill a significant portion of a pest population and sometimes provide the only feasible method for preventing economic loss. However, pesticides pollution is also recognized as a major health hazard to human beings and to natural enemies. Hence, many scholars put forward Integrated Pest Management (IPM) (see [1, 3, 4, 11]), IPM is a pest management system that in the context of the associated environment and the population dynamics of the pest species, utilizes all suitable techniques and methods in as a compatible manner as possible and maintains the pest populations at levels below those causing economic injury.

Recently, the models for pest control were studied by some authors ([2-6]) and some results were obtained. As we all know, most of the research literature on these epidemic models assumed that the disease incubation is negligible, so that, once infected, each susceptible individual (S) instantaneously becomes infectious (I) and later recovers (R) with a permanent or temporary acquired immunity. A model based on these assumptions is often called an SIR or SIRS model. The SIR epidemiological model was studied in [7], they assumed that the susceptible satisfied the logistic equation and the incidence rate was of the form kISq and the total population was not constant.

However, it is inevitable that IPM may cause pollution to the environment more or less due to the use of chemical pesticide. Therefore, in this paper we propose a biological control strategy-controlling the pest by introducing micro-bial pesticide and infected pests simultaneously. Compared with the chemical pesticide, the application shows that the microbial pesticide is an effective, highly infectious and safe bio-pesticide which can be used in both short-term and long-term controls and plays an important role in pest management.

The model we consider is based on the following SI model:

where S(t) and I(t) are densities of the susceptible and infectious, respectively, β > 0 is called the transmission coefficient, d > 0 is the death rate of the infectious pests.

For IPM strategy, we combine the biological control and chemical control. The infectious pests are released periodically every time period τ, meanwhile periodic spraying the microbial pesticide for susceptible pests. Based on biological control strategy in pest management, we construct a pest-epidemic model with impulsive control. Impulsive differential equations found in almost every domain of applied science and have been studied in many investigations ([813]). But to our knowledge there are only a few papers and books on mathematical model of the dynamics of microbial diseases in pest control. Li et al. [14], Anderson et al. [15] and Jong et al. [16] pointed out that standard incidence is more suitable than bilinear incidence. Levin et al. [17] have adopted a incidence form like βSlIh or l > 0, h > 0 which depends on different infective diseases and environment. So we develop (1.1) by introducing a constant periodic releasing of the infective pests and spraying microbial pesticides at fixed moment. That is, we consider the following impulsive differential equations:

where ΔS(t) = S(t+) - S(t), ΔI (t) = I (t+) - I (t). S(t) is in the absence of I (t) grows logistically with carrying capacity K, and with an intrinsic birth rate constant r, the nonlinear incidence rate was of the form β SIq, q > 1; 0 < µ1 < 1 represents the fraction from susceptible to infectious due to spraying the microbial pesticide at t = nτ ;0 < µ2 < 1, 0 < µ3 < 1 which represent the traction of susceptible and infective pests due to spraying pesticides at t = nτ, respectively; and 0 < θ < 1, µ1 + µ2 < 1; p > 0 is the release amount of the infected pests at t = nτ, n ∈ N, N = {0, 1, 2, · · ·}, τ is the period of the impulsive effect. That is, we can use a combination of biological and chemical tactics to eradicate pests or keep the pest population below the damage level.

2 Notations and definitions

In this section, we give some notations which will prove useful and give some definitions.

Let R+ = [0, ∞), = {x ∈ R2: x > 0}, Ω = int , N be the set of all nonnegative integers. Denote f = (f1, f2), the map defined by the right hand side of the first two equations of system (1.2). Let V0= {V: R+ × → R+}, continuous on (nτ, (n + 1)τ] × , and lim(t,y)→(nτ+ ,x)V(t, y) = V(nτ+, x) exists.

Definition 2.1.VV0, then for (t, x) ∈ (nτ, (n + 1)τ ] × , the upper right derivative of V(t, x) with respect to the impulsive differential system (1.2) is defined as

The solution of system (1.2) is a piecewise continuous function x : R+, x(t) is continuous on (nτ, (n + 1)τ], n ∈ N and x(nτ+) = lim t → nτ + x(t) exists. Obviously the smoothness properties of f guarantee the global existence and uniqueness of solution of system (1.2), for details (see [18]).

We will use a basic comparison result from impulsive differential equations. For convenience, we state it in our notations.

Suppose satisfies:

(H) g is continuous in and for exists.

Lemma 2.2.Let VV0, assume that

where g: R+ x R+R satisfies (H) and is nondecreasing. Let h (t) be the maximal solution of the scalar impulsive differential equation

existing on [0, ∞). Then V(0+, x0) < u0implies that V(t, x(t)) < h(t), t > 0, where x (t) is any solution of (1.2), similar result can be obtained when all the directions of the inequalities in the lemma are revered and Ψn is nonincreasing. Note that if we have some smoothness conditions of g to guarantee the existence and uniqueness of solutions for (2.2), then h(t) is exactly the unique solution of (2.2).

Lemma 2.3.Suppose that x (t) is a solution of system (1.2) with x (0+) > 0, then x (t) > 0 for all t > 0. Further, if x (0+) > 0, then x (t) > 0 for all t > 0.

For convenience, we give some basic properties of the following system

Then we have the following lemma:

Lemma 2.4.System (2.3) has a unique positive periodic solution with period τ and for every solution I (t) of (2.3) such that as t → ∞, where

and is globally asymptotically stable. Hence the solution of (2.3) is

Lemma 2.5.There exists a constant M > 0 such that S(t) < M, I(t) < M for each positive solution x(t) = (S(t), I(t)) of (1.2) with all t large enough.

Proof. Define V(t, x(t)) = S(t) + I(t). Then V(t, x(t)) ∈ V0 and the upper right derivative of V(t, x (t)) along solution of (1.2) is described as

where

when t = nτ, we obtain

According to Lemma 2.2, for t ∈ (nτ, (n + 1)τ), we have

Definition 2.6.System (1.2) is said to be permanent if there exists positive constants m ,M such that each positive solution (S(t), I (t)) of system (1.2) satisfies m < S(t) <M,m < I (t) <M for all t sufficiently large.

3 Stability of the pest-eradication periodic solution

In this section, we study the stability of the pest-eradication periodic solution of system (1.2).

Theorem 3.1. The pest-eradication periodic solution of system (1.2) is globally asyptotically stable provided

Proof. Firstly, we prove the local stability of a τ-period solution may be determined by considering the behavior of small-amplitude perturbations (u (t), v(t)) of the solution.

Define

where u(t), v(t) are small perturbations, there may be written as

where Φ(t) satisfy

where Φ(0) is the identity matrix. The resetting impulsive conditions of (1.2) becomes

Hence, if absolute values of all eigenvalues of

are less than one, the τ-periodic solution is locally stable. By calculating, we have

there is no need to calculate the exact form of (*) as it is not required in the analysis that follows. Then the eigenvalues of M denoted by λ1, λ2 are the following:

λ1 < 1 if (3.1) holds true. According to Floquet theory, the pest-eradication solution is locally asymptotically stable.

In the following, we prove the global attractivity. Choose a sufficiently small ε > 0 such that

Noting that and as t = nτ, consider the following impulsive differential equation:

by Lemma 2.4, system (3.2) has a globally asymptotically stable positive periodic solution

So by Lemmas 2.2 and 2.4, we get

From system (1.2), we obtain that

Integrating (3.4) on (nτ, (n + 1)τ], which yields

Thus, S(nτ) < S(0)δn and S(nτ) → 0 as n → ∞. Therefore, S(t) → 0 as t → ∞, since 0 < S(t) < (1 - µ1 - µ2)S(nτ) exp(r τ) for nτ < t < (n + 1)τ.

Next, we prove that for a sufficiently small 0 < ε < there exists a T1> 0 such that 0 < S(t) < ε for all t > T1. From system (1.2), we have

considering the following comparison system

By Lemma 2.4, system (3.7) has a positive periodic solution

which is globally asymptotically stable. Thus, for a sufficiently small ε1, there exists a T2> T1> 0 such that t > T2

Combining (3.3) and (3.8), we obtain for t large enough, let This completes the proof.

4 Permanence

Theorem 4.1.System (1.2) is uniformly permanent if

Proof. Suppose x(t) = (S(t), I(t)) is a solution of (1.2) with x(0) > 0, from Lemma 2.5, we may assume S(t) < µ, I(t) < µ and for t large enough.

sufficiently small.

According to Lemmas 2.2 and 2.4, we have I(t) > m2 for t large enough. So, if we can find positive number such that for t large enough, then our aim is obtained.

Next, we will do it in the following two steps for convenience.

Step I: If (4.1) holds true, we can choose and Ε3 small enough such that

we will prove there exist a such that S(t1) > m 1. Otherwise S(t) < m 1 for all t > 0. From system (1.2), we obtain that

consider the following comparison system

by Lemmas 2.2 and 2.4 on (4.3), we have where

Therefore, there exists a T3> 0 such that

for t > T3. Thus

for t > T3, integrating (4.4) on (nτ, (n + 1)Τ], n > N1, here N1 is a nonneg-ative integer and N1τ > T3, then we obtain

Then which is a contradiction to S(t) < m 1 for all t > 0. Hence there exists a t1 such that S(t1) > m1.

Step II: If S(t) > m1 for all t > t1, then our aim is obtained. Otherwise S(t) < m1 for some t > t1, setting t* = inft>t1{S(t) < m1}, there are the following two cases for t*:

Case (a): If t* = n1τ, n1 is some positive integer. In this case S(t) > m1 for t ∈ [t1, t*) and (1 - µ1 - µ2)S(t*+) = (1 - µ1 - µ2)S(t*) < m1. Let T4= Η2τ + n3Τ, where n2= n'2 + n2'''n'2 , n'»2 and n3 satisfy the following inequalities:

where

We claim that there must be a time t2 ∈ (t*, t* + T4) such that S(t2) > m 1, if it is not true, i.e., S(t) < m 1, t ∈ (t*, t* + T4), similar to the analysis before, we consider system (4.3) with initial value z(t*+) = I(t*+) > 0, by Lemma 2.4, we have

for t ∈ (nτ, (n + 1)τ], n1< Η < n1 + n2 + n3. Then

and which implies that system (4.4) holds for [t* + Η2τ, t* + T4], integrating system (4.4) on this interval, we have

In addition, we have

Integrating system (4.6) on the interval [t*, (n1 + n2)τ], which yields

combining (4.5) and (4.7), we have

which is a contradiction, so there exists a time t2 ∈ [t*, t* + T4] such that since 0 < µ1 + µ2 < 1, S(nτ+) = (1 - µ1 - µ2)S(nτ) < S(nτ) and Thus, suppose is a positive integer and l < n2 + n3, from system (4.6), we have

for The same arguments can be continued since Hence for all t > t1.

Case (b): If t* ≠ Η Τ, then S(t*) = m 1 and S(t) > m 1, t ∈ [t1, t*], suppose t* e (n'1Τ, (n'1 + 1)τ], we also have two subcases for t ∈ [t*, (n'1 + 1)τ] as follows:

Case (i): S(t) < m 1, t ∈ [t*, (n'1 + 1)τ], we claim that there exists a t'2 ∈ [n'1τ, (n'1 + 1)τ + T4] such that S(t'2) > m 1. Otherwise integrating system (4.6) on the interval [(n'1 + 1 + n2)τ, (n'1 + 1 + n2 + n3)τ] produces

Since S(t) < m 1, t ∈ [t*, (n'1 + 1)τ], system (4.7) holds on [t*, (n'1 + 1 + n2 + n3)τ], thus

and

which is a contradiction. Let and Choose is a positive integer and l' < 1 + n2 + n3, we have

so we have For the same argument can be continued since

Case (ii): If there exists a t(t*, (n'1 + 1)τ] such that S(t) > m 1. Let then and . For (4.6) holds and integrating (4.6) on we have

Since the same argument can be continued. Hence, we have Thus in both cases, we conclude S(t) > m 1 for all t > t1. The proof is complete.

Remark 1. Let

Since and f'(τ) > 0, so f (τ) = 0 has a unique positive root, denoted by τmax From Theorem 3.1 and Theorem 4.1, we know that the pest-eradication periodic is globally asymptotically stable when τ <τmax If τ > τmax the system (1.2) is permanence.

Remark 2. If µ1= µ2= µ3= 0, that is, we only choose the biological control, we can obtain that τ0 is the threshold and τmax> τ0, which implies that we must release more infected pest to eradicate the pests. If p = 0, that is there is no periodic releasing infective pests, so we can easily obtain that is the threshold and τmax> τ1, it is obviously, impulsive releasing pests may lengthen the period of spraying pesticides and therefore reduce the cost of pests control.

5 Numerical analysis and conclusion

In this paper, we have investigated dynamical behaviors of an SI model with impulsive transmitting infected pests and spraying pesticides at fixed moment. The purpose of this paper is the behavior of an impulsively controlled integrated pest management model. To limit the damaging potential of the pest population, a biological control, consisting in the release of infective pests, and a chemical control, consisting in pesticide spraying, are applied in pest management. An unspecified nonlinear force of infection is assumed to describe the transmission of the disease which is spread through the release of infected individuals, and it is assumed that the infective pest population neither damages the crops, nor reproduces. We have shown that there exists an asymptotically stable the susceptible pest-eradication periodic solution if impulsive period is less than some threshold. When the stability of pest-eradication periodic solution is lost, system (1.2) is permanent, which is in line with reality from a biological point of view. Numerical results show that system (1.2) can take on various kinds of periodic fluctuations, which implies that the presence of pulse makes the dynamic behavior more complex (see Fig. 3).




It is observed that, theoretically speaking, the control strategy can be always made to succeed by the use of proper pesticides, while as far as the biological control is concerned, its sufficient effectiveness can also be reached provided that the numbers µi- (i = 1, 2, 3) of infected pests released each time or the period τ is proper, that is, from Theorem 3.1 and Theorem 4.1, we know that the pest-eradication periodic is globally asymptotically stable when τ <τmax (see Fig. 1). If τ >τmax the system (1.2) is permanence (see Fig. 2). Any of these features alone can ensure the global success of our control strategy, although in concrete situations these may or may not be biologically feasible or may require a large amount of resources.

To facilitate the interpretation of our mathematical findings by numerical analysis, we consider the hypothetical set of parameter values as r = 1, θ = 0.91, β = 2, d = 0.98, q = 1.8, p = 0.4, µ1= 0.7, µ2= 0.1, µ3= 0.1, τmax = 1.838045.

Received: 10/III/10.

Accepted: 28/IV/10.

#CAM-192/10.

  • [1] C.B. Huffaker, New technology of pest control. Wiley, New York (1980).
  • [2] H.J. Barclay, Models for pest control using predator release, habitat management and pesticide release in combination. J. Appl. Ecol., 19 (1982), 337-348.
  • [3] X. Wang and X.Y. Song, Analysis of an impulsive pest management SEI model with nonlinear incidence rate. Computational & Applied Mathematics, 29 (2010), 1-17.
  • [4] S.Y. Tang, Y.N. Xiao, L.S. Chen and R.A. Cheke, Integrated pest management models and their dynamical behavior. Bull. Math. Biol., 67 (2005), 115-135.
  • [5] J.C. Van Lenteren, Integrated pest management in protected crops, in Integrated Pest Management. D. Dent (Ed.), Chapman and Hall, London, (1995), 311-320.
  • [6] X. Wang and X.Y. Song, A predator-prey system with two impulses on the diseased prey and a Beddington-DeAngelis response. Math. Meth. Appl. Sci., 33 (2010), 303-312.
  • [7] X.A. Zhang and L.S. Chen, The periodic solution of a class of epidemic models. Comput. Math. Appl., 38 (1999), 61-71.
  • [8] X. Wang and X.Y. Song, Mathematical models for the control of a pest population by infected pest. Computers & Mathematics with Applications, 56 (2008), 266-278.
  • [9] Z. Agur, L. Cojocaru, R. Anderson and Y. Danon, Pulse mass measles vaccination across age cohorts. Proc. Natl Acad. Sci. USA, 90 (1993), 11698-11702.
  • [10] G. Ballinger and X.N. Liu, Permanence of population growth models with impulsive effects. Math. Comput. Modelling, 26 (1997), 59-72.
  • [11] J.J. Jiao and L.S. Chen, A pest management SI model with periodic biological and chemical control concern. Appl. Math. Comput., 183 (2006), 1018-1026.
  • [12] H. Zhang and L.S. Chen, Pest management through continuous and impulsive control strategies. BioSystems, 90 (2007), 350-361.
  • [13] X. Wang, Y.D. Tao and X.Y. Song, Mathematical model for the control ofa pest population with impulsive perturbations on diseased pest. Applied Mathematical Modelling, 33 (2009), 3099-3106.
  • [14] Y.F. Li and X.Y. Song, Dynamic complexities of a Holling II two-prey one-predator system with impulsive effect. Chaos, solitons and Fractals, 33 (2007), 463-478.
  • [15] R. Anderson and R. May, Infectious Diseases ofHuman: Dynamics and Control. Oxford University Press (1991).
  • [16] M.C.M. De Jong, O. Diekmann and H. Heesterbeek, How does transmission depend on population size? In: D. Mollison (Ed.), Human Infectious Diseases, Epidemic Models, Cambridge University Press, Cambridge, UK (1995), pp. 8494.
  • [17] W.M. Liu, S.A. Levin and Y. Lwasa, Influence of nonlinear incidence rates upon the behavior of SIRSEpidemiological models. J. Math. Biol., 25 (1987), 359-380.
  • [18] V. Lakshmikantham, D.D. Bainov and P.S. Simeonov, Theoryofimpulsive differential equations. World Scientific, Singapore (1989).
  • *
    Supported by the National Natural Science Foundation of China (No. 10771179), the Natural Science Foundation of the Education Department of Henan Province (No. 2010B110019), the Youth Science Foundation of Xinyang Normal University (20100070), the Young Backbone Teacher Foundation of Xinyang Normal University.
  • Publication Dates

    • Publication in this collection
      27 July 2011
    • Date of issue
      2011

    History

    • Received
      10 Mar 2010
    • Accepted
      28 Apr 2010
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