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Delay effect in the Nicholson’s blowflies model with a nonlinear density-dependent mortality term

Wanmin Xiong

B

Furong College, Hunan University of Arts and Science, Changde 415000, Hunan, P. R. China Received 20 January 2017, appeared 30 March 2017

Communicated by Leonid Berezansky

Abstract. This paper is concerned with a class of non-autonomous delayed Nicholson’s blowflies model with a nonlinear density-dependent mortality term. Under proper conditions, we prove that the positive equilibrium point is a global attractor of the addressed model with small delays. Moreover, some numerical examples are given to illustrate the feasibility of the theoretical results.

Keywords: Nicholson’s blowflies model, nonlinear density-dependent mortality term, time-varying delay, global attractivity.

2010 Mathematics Subject Classification: 34C25, 34K11, 34K25.

1 Introduction

Recently, based on that marine ecologists are currently constructing new fishery models with nonlinear density-dependent mortality rates, the following Nicholson’s blowflies model with a nonlinear density-dependent mortality term

N0(t) =−D(N(t)) +PN(t−τ)eN(tτ), (1.1) was proposed in L. Berezansky et al. [1]. Here function D(x)might have one of the following forms: D(N) = baN+N or D(N) = a−beN with positive constants a,b > 0. The detailed biological explanations of the parameters of (1.1) can be found in [1,13]. Furthermore, (1.1) and its generalized equations have been extensively studied, and this extensive study has produced a lot of progress on the existence and stability of positive equilibrium point, positive periodic solutions, and positive almost periodic solutions, see more details in [2–4,8,11–13,18].

In particular, the author in [9] established several criteria on the global asymptotic stability of zero equilibrium point for the following Nicholson’s blowflies model with a nonlinear density-dependent mortality term:

N0(t) =−a+beN(t)+

m j=1

βjN(t−τj(t))eγjN(tτj(t)), (1.2)

BEmail: wanminxiong2009@aliyun.com

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wherea, b, βj, γj are positive constants,τj(t)≥0 is a bounded and continuous function, and j∈ J ={1, 2, . . . ,m}.

On the other hand, the effect of delay on the asymptotic behavior of population models can reveal the essential characteristics of time delay in practical problems, and it has attracted extensive attention in [5,6,15,17]. It is worthy mentioned that there have been few papers concerning the effect of delay on the dynamical behavior of the delayed Nicholson’s blowflies model with a nonlinear density-dependent mortality term.

Motivated by the above works, the effect of delay on the dynamical behavior of the delayed Nicholson’s blowflies model with a nonlinear density-dependent mortality term attracted our attention. In this paper, we aim to provide a criterion to guarantee that all solutions of (1.2) converge to the positive equilibrium point, which entails that (1.2) is global attractive under the small delays. In fact, one can see the following Remark2.2and Remark3.1for details.

In what follows, we designate r = max1jmsuptRτj(t), C = C([−r, 0],R) be the continuous functions space equipped with the usual supremum norm k · k, and let C+ = C([−r, 0],(0,+)). If x(t)is continuous and defined on [−r+t0, σ)with t0,σR, then we definext ∈Cwhere xt(θ) =x(t+θ)for allθ ∈[−r, 0].

It will be always assumed that γ = min

1jmγj >0, γ= max

1jmγj ≥1,

m j=1

βj γja

1

e <1, and lnb a > 1

γ. (1.3) Denote Nt(t0,ϕ) (N(t;t0,ϕ)) as an admissible solution of (1.2) with the admissible initial condition

Nt0 = ϕ, ϕ∈C+ and ϕ(0)>0. (1.4) and[t0,η(ϕ))be the maximal right-interval of the existence of Nt(t0,ϕ). Define a continuous functionF:R→Rby setting

F(u) =−a+beu+

m j=1

βjueγju. Since

F(0) =−a+b>0, F(+) =−a<0, there exists at least one positive constant ¯Nsuch that

F(N¯) =−a+beN¯ +

m j=1

βjNe¯ γjN¯ =0, (1.5) which is a positive equilibrium point of (1.2).

2 Main result

In this section, we establish some sufficient conditions on the global asymptotic stability of positive equilibrium point for (1.2).

Lemma 2.1. N(t;t0,ϕ)is positive and bounded on[t0,η(ϕ))and henceη(ϕ) = +∞. Moreover, l=lim inf

t→+ N(t;t0,ϕ)≥lnb a > 1

γ. (2.1)

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Proof. LetN(t) =N(t;t0,ϕ). We first claim:

N(t)>0 for allt∈ [t0,η(ϕ)).

Suppose, for the sake of contradiction, there existst1∈(t0, η(ϕ))such that N(t1) =0, N(t)>0 for allt ∈[t0,t1).

Then,

0≥ N0(t1) =−a+beN(t1)+

m j=1

βjN(t1τj(t1))eγjN(t1τj(t1))≥ −a+b>0.

This contradiction means that N(t)>0 for allt ∈[t0,η(ϕ)). For eacht∈[t0−r,η(ϕ)), we define

M(t) =max

ξ :ξ ≤t,x(ξ) = max

t0rstN(s)

.

We now show that N(t)is bounded on [t0,η(ϕ)). In the contrary case, observe that M(t)→ η(ϕ)ast →η(ϕ), we have

tlimη(ϕ)N(M(t)) = +∞.

On the other hand,

N(M(t)) = max

t0rstx(s), and so N0(M(t))≥0, where M(t)>t0. Thus, in view of the fact that supu0ueu= 1e, we get

0≤ N0(M(t))

= −a+bex(M(t))+

m j=1

βjN(M(t)−τj(M(t)))eγjN(M(t)−τj(M(t)))

= a

"

−1+ b

aeN(M(t))+

m j=1

βj

γjaγjN(M(t)−τj(M(t)))eγjN(M(t)−τj(M(t)))

#

≤ a

"

−1+ b

aeN(M(t))+

m j=1

βj γja

1 e

#

, where M(t)>t0. Lettingt →η(ϕ)leads to

0≤ −1+

m j=1

βj γja

1 e,

which contradicts to the assumption (1.3). This implies that x(t) is bounded on [t0,η(ϕ)). From Theorem 2.3.1 in [7], we easily obtainη(ϕ) = +∞.

Let l = lim inft→+N(t). By the fluctuation lemma [16, Lemma A.1], there exists a sequence {tp}p1such that

tp →+∞, N(tp)→lim inf

t→+ N(t), N0(tp)→0 as p→+∞.

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According to (1.2), we get

N0(tp) =−a+beN(tp)+

m j=1

βjN(tpτj(tp))eγjN(tpτj(tp))

≥ −a+beN(tp),tp >t0. Then, taking limits gives us that

l= lim inf

t→+ N(t)≥lnb a > 1

γ. This ends the proof of Lemma2.1.

Remark 2.2. From Lemma2.1, it is not difficult to see that (1.2) and (1.4) is uniformly perma- nent. Moreover, ¯Nis also a solution of (1.2) and (1.4), and

N¯ ≥lnb a > 1

γ. (2.2)

For simplicity, denoteN(t;t0,ϕ)byN(t). Now, we show the global attractivity of ¯Nby the following three propositions:

Proposition 2.3. If x(t) = N(t)−N is eventually nonnegative, then¯

t→+limN(t) =N.¯ Proof. Clearly, there existsT>t0 such that

x(t) = N(t)−N¯0 for allt≥ T.

In order to prove Proposition 2.3, it suffices to show that lim supt→+x(t) = 0. Again by way of contradiction, we assume that lim supt→+x(t) > 0. By the fluctuation lemma [16, Lemma A.1], there exists a sequence{tk}k1 such that

tk →+∞, x(tk)→lim sup

t→+

x(t), x0(tk)→0 ask →+∞.

In view of (2.2), we can chooseK>Tto satisfy that γjN(t)≥γjN¯ >γj 1

γ ≥1, for allt >K, j∈ J, which, together with the fact thatxex decreases on[1, +), implies that

x0(tk) = −a+beN(tk)+

m j=1

βjN(tkτj(tk))eγjN(tkτj(tk))

= −a+beN(tk)+

m j=1

βj

γjγjN(tkτj(tk))eγjN(tkτj(tk))

≤ −a+beN(tk)+

m j=1

βj

γjγjNe¯ γjN¯, tk > K+r. (2.3) By taking limits, (1.5) and (2.3) lead to

0≤ −a+be−(lim supt→+x(t)+N¯)+N¯

m j=1

βjeγjN¯ <−a+beN¯ +N¯

m j=1

βjeγjN¯ =0, a contradiction. Hence, lim supt→+x(t) =0. This completes the proof.

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Proposition 2.4. If x(t) =N(t)−N is eventually non-positive, then¯

t→+limN(t) = N.¯ Proof. Obviously, we can chooseT>t0such that

x(t) =N(t)−N¯ ≤0 for all t≥T.

Next, we prove that lim inft→+x(t) = 0. Otherwise, lim inft→+x(t) < 0. Again from the fluctuation lemma [16, Lemma A.1], there exists a sequence{t¯k}k1such that

k →+∞, x(¯tk)→lim inf

t→+ x(t), x0(t¯k)→0 ask →+∞.

From (2.1), we can chooseK > Tto satisfy that γjN¯ ≥γjN(t)>γj 1

γ ≥1, for allt >K, j∈ J, which, together with the fact thatxex decreases on[1, +), implies that

x0(t¯k) = −a+beN(t¯k)+

m j=1

βjN(t¯kτj(¯tk))eγjN(t¯kτj(t¯k))

= −a+beN(t¯k)+

m j=1

βj

γjγjN(¯tkτj(t¯k))eγjN(t¯kτj(¯tk))

≥ −a+beN(t¯k)+

m j=1

βj

γjγjNe¯ γjN¯, tk >K+r. (2.4) By taking limits, (1.5) and (2.4) give us that

0≥ −a+be−(lim inft→+x(t)+N¯)+N¯

m j=1

βjeγjN¯ >−a+beN¯ +N¯

m j=1

βjeγjN¯ =0, a contradiction and hence lim inft→+x(t) =0. This completes the proof.

Proposition 2.5. If x(t) =N(t)−N oscillates about zero, and¯ r

e

m j=1

βj <1, γra

1−remj=1βj ≤1 (2.5) thenlimt→+N(t) = N.¯

Proof. Sety(t) =γx(t) =γ(N(t)−N¯), we have y0(t) = −γa+γbeN¯1γy(t)+γ

m j=1

βj

N¯ + 1

γy(t−τj(t))

eγjN¯

γj

γy(tτj(t))

, t >t0. (2.6) Let

λ=lim inf

t→+ y(t), µ=lim sup

t→+

y(t). (2.7)

Sincey(t) =γx(t)oscillates about zero, one can get that λ0µ.

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Now, in order to prove Proposition2.5, it suffices to show that thatλ=µ=0.

Again from the fact thaty(t)oscillates about zero, we can choose a strictly monotonically increasing sequence{qn}n1 to satisfy that

qn>r, lim

n→+qn= +∞, y(qn) =0 for alln=1, 2, . . . ,

and such that in each interval(qn,qn+1)the function y(t)assumes both positive and negative values. For any positive integern, lettn,sn ∈(qn,qn+1)such that

y(tn) = max

t∈[qn,qn+1]y(t)>0, y(sn) = min

t∈[qn,qn+1]y(t)<0.

Then,

y0(tn) =y0(sn) =0, n=1, 2, . . . , (2.8) and

λ=lim inf

t→+ y(t) =lim inf

n→+ y(sn), µ=lim sup

t→+

y(t) =lim sup

n→+

y(tn). (2.9) Subsequently, we assert that for each positive integern, there isTn∈[tn−r,tn)∩[qn,tn)such that

y(Tn) =0, and y(t)>0 for all t∈(Tn,tn). (2.10) In the contrary case, given a positive integern, we have

qn <tn−r <qn+1 and y(t)>0 for allt∈ [tn−r,tn),

which, together with (1.5), (2.2), (2.6), (2.8) and the fact that xex decreases on [1,+), tells us that

0= −γa+γbeN¯1γy(tn)+γ

m j=1

βj

N¯ + 1

γy(tnτj(tn))

eγjN¯

γj

γy(tnτj(tn))

= −γa+γbeN¯1γy(tn)+γ

m j=1

βj 1 γj

γjN¯ +γj

γy(tnτj(tn))

eγjN¯

γj

γy(tnτj(tn))

< −γa+γbeN¯ +γ

m j=1

βj 1

γjγjNe¯ γjN¯

= −γa+γbeN¯ +γ

m j=1

βjNe¯ γjN¯

=0.

This is a contradiction and proves (2.10).

Similarly, we can prove that for each positive integer n, there isSn ∈ [sn−r,sn)∩[qn,sn) such that

y(Sn) =0, and y(t)<0 for allt ∈(Sn,sn). (2.11) For anyε>0, (2.9) implies that there exists a positive integernsuch that min{tn,sn} −2r>

t0, and

λε<y(t)<µ+ε for all t>min{tn,sn} −2r. (2.12) Thus,

y(t−τj(t))e

γj

γy(tτj(t)) <µ+ε for allt>min{lq,sq} −r, j∈ I. (2.13)

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In view of (1.3), (2.2), (2.10), (2.12) and (2.13), integrating (2.6) from Tntotn, we find y(tn) = −γa(tn−Tn) +γb

Z tn

Tn

eN¯γ1y(t)dt +γ

m j=1

βj Z tn

Tn

N¯ + 1

γy(t−τj(t))

eγjN¯

γj

γy(tτj(t))

dt

= −γa(tn−Tn) +γb Z tn

Tn

eN¯e1γy(t)dt +

m j=1

βj Z tn

Tn

γNe¯ γjN¯e

γj

γy(tτj(t))

+eγjN¯y(t−τj(t))e

γj

γy(tτj(t)) dt

< −γa(tn−Tn) +γbeN¯e−(λε)(tn−Tn) + (tn−Tn)

m j=1

βj h

γNe¯ γjN¯e−(λε)+eγjN¯(µ+ε)i

= γ(tn−Tn)

"

beN¯ +

m j=1

βjNe¯ γjN¯

!

e−(λε)−a

#

+ (tn−Tn)

m j=1

βjeγjN¯(µ+ε)

< γrah

e−(λε)−1i + r

e

m j=1

βj(µ+ε), n>n. (2.14)

Lettingn→+andε →0+, (2.5) and (2.14) give us that µγra

1− remj=1βj(eλ−1)≤ eλ−1. (2.15) Furthermore, from (1.3), (2.2), (2.6), (2.11) and (2.12), we obtain

y(sn) = −γa(sn−Sn) +γb Z sn

Sn

eN¯1γy(t)dt +γ

m j=1

βj Z sn

Sn

N¯ + 1

γy(t−τj(t))

eγjN¯

γj

γy(tτj(t))

dt

> −γa(sn−Sn) +γb(sn−Sn)eN¯e−(µ+ε) +γ

m j=1

βj Z sn

Sn

N¯ + 1

γy(t−τj(t))

eγjN¯−(µ+ε)dt

> −γa(sn−Sn) +γb(sn−Sn)eN¯e−(µ+ε) + (sn−Sn)

m j=1

βj h

γNe¯ γjN¯e−(µ+ε)+eγjN¯(λε)e−(µ+ε)i

> −γa(sn−Sn) +γb(sn−Sn)eN¯e−(µ+ε) + (sn−Sn)

m j=1

βj h

γNe¯ γjN¯e−(µ+ε)+eγjN¯(λε)i

=γ(sn−Sn)

"

(beN¯ +

m j=1

βjNe¯ γjN¯)e−(µ+ε)−a

#

+ (sn−Sn)

m j=1

βjeγjN¯(λε)

>γra[e−(µ+ε)−1] +r e

m j=1

βj(λε), n>n. (2.16)

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Lettingn →+andε→0+, (2.5) and (2.16) lead to λγra

1− remj=1βj(eµ−1)≥eµ−1. (2.17) Thus, we have from (2.15) and (2.17) that

eµ1λµ≤eλ1.

According to the proof in Theorem 4.1 of [17], one can show λ = µ = 0. This ends the proof.

By Propositions2.3,2.4and2.5, we have the following result.

Theorem 2.6. Suppose that (2.5) holds, then the positive equilibrium point N of¯ (1.2) is a global attractor.

Remark 2.7. Since

rlim0+

r e

m j=1

βj =0, lim

r0+

γra 1−remj=1βj

=0,

then condition (2.5) naturally holds under the sufficiently small delay, and the positive equi- librium point ¯N is a global attractor of (1.2) with the small delays. Moreover,

r→+lim r e

m j=1

βj = +

implies that condition (2.5) is not satisfied when the delays in (1.2) is sufficiently large.

3 An example

In this section, we will give an example to verify the correctness of our main results obtained in previous section. Considering the following Nicholson’s blowflies model with a nonlinear density-dependent mortality term:

N0(t) =−11

10 +e2eN(t)+ e

2

40N(t−τ)eN(tτ)+ e

2

40N(t−2τ)eN(t). (3.1) Obviously,

r =2τ, a= 11

10, b=e2, β1= β1= e

2

40, γ1=γ2 =1, N¯ =2.

If we choose τ = 0.1, it is straight to check that (3.1) satisfies (1.3) and (2.5). It follows from Theorem2.6that the positive equilibrium point 2 is a global attractor of (3.1). Fig.3.1supports this result with the numerical solutions of system (3.1) with different initial values. Moreover, if we choose τ = 10, then, (3.1) does not satisfy (2.5), we give the numerical simulations in Fig.3.2 to show that 2 is no longer a global attractor of (3.1). This implies that a small delay does not affect the asymptotic behavior of system (3.1), and large delay will cause the complex dynamic behavior of this system.

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0 2 4 6 8 10 0.5

1 1.5 2 2.5 3

t

N

N(t)

Figure 3.1: Numerical solutions of (3.1) with τ = 0.1 and initial values ϕ(s) = 0.6, 1.5, 2.7, s∈[−0.2, 0].

0 10 20 30 40 50 60 70 80 90 100

6 6.5 7 7.5 8 8.5 9 9.5

t

N

N(t)

Figure 3.2: Numerical solutions of (3.1) with τ = 10 and initial value ϕ(s) = 8.6, s∈[−20, 0].

Remark 3.1. The effect of delay on the asymptotic behavior plays an important role in de- scribing the dynamics of population models [10,14]. Thus it has been extensively studied by many scholars in recent decades. In this article, we first studied the effect of delay on the asymptotic behavior of Nicholson’s blowflies model with a nonlinear density-dependent mor- tality term. By means of the fluctuation lemma and some differential inequality technique, delay-dependent criteria are obtained for the global attractivity of the considered model. The sufficient condition, which is easily checked in practice, has a wide range of application. This implies that the obtained results in this article are completely new and extend previously known studies to some extent. In addition, the method in this paper can be applied to study the effect of the delay on the asymptotic behavior for some other dynamical systems. Also, it is natural to ask whether the delay affects the dynamical behavior of the addressed systems involving time-varying delays and time-varying coefficients. We leave this as our future work.

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Acknowledgements

The author would like to express the sincere appreciation to the associate editor and reviewers for their helpful comments in improving the presentation and quality of the paper.

This work was supported by the Natural Scientific Research Fund of Hunan Provincial of China (grant numbers 2016JJ6103 and 2016JJ6104), the Natural Scientific Research Fund of Hunan Provincial Education Department of China (2017, Study on dynamics of a class of biological models with feedback delays) and the Construction Program of the Key Discipline in Hunan University of Arts and Science – Applied Mathematics.

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