Delay-Induced Oscillations in a Competitor-Competitor-Mutualist Lotka-Volterra Model
Hindawi
Complexity
Volume 2017, Article ID 2578043, 12 pages
https://doi.org/10.1155/2017/2578043
Research Article
Delay-Induced Oscillations in a
Competitor-Competitor-Mutualist Lotka-Volterra Model
Changjin Xu
Guizhou Key Laboratory of Economics System Simulation, Guizhou University of Finance and Economics, Guiyang 550004, China
Correspondence should be addressed to Changjin Xu;
Received 14 January 2017; Accepted 30 March 2017; Published 26 April 2017
Academic Editor: Alicia Cordero
Copyright © 2017 Changjin Xu. 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.
This paper deals with a competitor-competitor-mutualist Lotka-Volterra model. A series of sufficient criteria guaranteeing the
stability and the occurrence of Hopf bifurcation for the model are obtained. Several concrete formulae determine the properties of
bifurcating periodic solutions by applying the normal form theory and the center manifold principle. Computer simulations are
given to support the theoretical predictions. At last, biological meaning and a conclusion are presented.
1. Introduction
The study of dynamical behaviors for tremendous predatorprey models has been a hot issue in population dynamics
in the past few decades. Many results have been reported
[1–11]. In the real world, any biological or environmental
parameters are naturally subject to fluctuation in time. The
effects of a periodically varying environment are important
for evolutionary theory as the selective forces on systems
in a fluctuating environment differ from those in a stable
environment. Meanwhile, time delay due to gestation is
common example because, generally, the consumption of
prey by the predator throughout its past history governs
the present birth rate of the predator. Based on all the
above point, Lv et al. [12] had investigated the periodic
solution of the following competitor-competitor-mutualist
Lotka-Volterra model by using Krasnoselskii’s fixed point
theorem
𝑥̇ 1 (𝑡) = 𝑥1 (𝑡) [𝑟1 (𝑡) − 𝑎11 (𝑡) 𝑥1 (𝑡 − 𝜏11 (𝑡))
𝑥̇ 1 (𝑡)
− 𝑎12 (𝑡) 𝑥2 (𝑡 − 𝜏12 (𝑡)) + 𝑎13 (𝑡) 𝑥3 (𝑡 − 𝜏13 (𝑡))] ,
𝑥̇ 2 (𝑡) = 𝑥2 (𝑡) [𝑟2 (𝑡) − 𝑎21 (𝑡) 𝑥1 (𝑡 − 𝜏21 (𝑡))
− 𝑎22 (𝑡) 𝑥2 (𝑡 − 𝜏22 (𝑡)) + 𝑎23 (𝑡) 𝑥3 (𝑡 − 𝜏23 (𝑡))] ,
𝑥̇ 3 (𝑡) = 𝑥3 (𝑡) [𝑟3 (𝑡) + 𝑎31 (𝑡) 𝑥1 (𝑡 − 𝜏31 (𝑡))
+ 𝑎32 (𝑡) 𝑥2 (𝑡 − 𝜏32 (𝑡)) − 𝑎33 (𝑡) 𝑥3 (𝑡 − 𝜏33 (𝑡))] ,
where 𝑥1 (𝑡) and 𝑥2 (𝑡) denote the densities of competing
species at time 𝑡 and 𝑥3 (𝑡) denotes the density of cooperating
species at time 𝑡. 𝑟𝑖 , 𝑎𝑖𝑗 ∈ 𝐶(𝑅, [0, ∞)) and 𝜏𝑖𝑗 ∈ 𝐶(𝑅, 𝑅) are
𝜔-periodic functions (𝜔 > 0). The parameters 𝜏𝑖𝑗 (𝑡) ≥ 0 (𝑖 =
1, 2, 3; 𝑗 = 1, 2, 3) are the feedback time delay of different
species. In detail, one can see [12].
It is well known that the research on the Hopf bifurcation,
especially on the stability of bifurcating periodic solutions
and direction of Hopf bifurcation, is one of the most important themes on the predator-prey dynamics. There are a
great deal of papers which deal with this topic [11, 13–22].
The purpose of this paper is to discuss the stability and the
properties of Hopf bifurcation of model (1). To simplify the
analysis for model (1), we make the following assumptions:
all biological and environmental parameters are constants in
time and only the feedback time delay of competing species
𝑥𝑖 (𝑖 = 1, 2) to the growth of the species itself and the
feedback time delay of cooperating species 𝑥3 to the growth
of the species itself exist and are the same. Then system (1) can
be described as the form
(1)
= 𝑥1 (𝑡) [𝑟1 − 𝑎11 𝑥1 (𝑡 − 𝜏) − 𝑎12 𝑥2 (𝑡) + 𝑎13 𝑥3 (𝑡)] ,
𝑥̇ 2 (𝑡)
= 𝑥2 (𝑡) [𝑟2 − 𝑎21 𝑥1 (𝑡) − 𝑎22 𝑥2 (𝑡 − 𝜏) + 𝑎23 𝑥3 (𝑡)] ,
𝑥̇ 3 (𝑡)
= 𝑥3 (𝑡) [𝑟3 + 𝑎31 𝑥1 (𝑡) + 𝑎32 𝑥2 (𝑡) − 𝑎33 𝑥3 (𝑡 − 𝜏)] .
(2)
2
Complexity
In this paper, we consider the effect of time delay 𝜏 on
the dynamics of system (2). We not only give the conditions
on the stability of the positive equilibrium of (2) and the
existence of periodic solutions but also derive the formulae
for determining the properties of a Hopf bifurcation.
The remainder of the paper is organized as follows.
In Section 2, we investigate the stability of the positive
equilibrium and the occurrence of local Hopf bifurcations.
In Section 3, the direction and stability of the local Hopf
bifurcation are established. In Section 4, numerical simulations are carried out to illustrate the validity of the main
results. Biological explanations and some main conclusions
are drawn in Section 5.
𝑥̇ 3 (𝑡) = 𝑑1 𝑥1 (𝑡) + 𝑑2 𝑥2 (𝑡) + 𝑑3 𝑥3 (𝑡 − 𝜏)
+ 𝑑4 𝑥1 (𝑡) 𝑥3 (𝑡) + 𝑑5 𝑥2 (𝑡) 𝑥3 (𝑡)
+ 𝑑6 𝑥3 (𝑡) 𝑥3 (𝑡 − 𝜏) ,
(4)
where
𝑏1 = −𝑎11 𝑥1∗ ,
𝑏2 = −𝑎12 𝑥1∗ ,
𝑏3 = 𝑎13 𝑥1∗ ,
𝑏4 = −𝑎11 ,
2. Stability of the Positive Equilibrium and
Local Hopf Bifurcations
𝑏5 = −𝑎12 ,
𝑏6 = 𝑎13 ,
Consider the realistic implication and actual application of
biological system; in this section, we shall only study the
stability of the positive equilibrium and the existence of local
Hopf bifurcations. It is easy to see that system (2) has a unique
positive equilibrium 𝐸0 (𝑥1∗ , 𝑥2∗ , 𝑥3∗ ) if the condition
sign {Δ} = sign {Δ 1 } = sign {Δ 2 } = sign {Δ 3 }
𝑐1 = −𝑎21 𝑥2∗ ,
𝑐2 = −𝑎22 𝑥2∗ ,
𝑐3 = 𝑎23 𝑥2∗ ,
(H1)
(5)
𝑐4 = −𝑎21 ,
𝑐5 = −𝑎22 ,
holds, where
𝑐6 = 𝑎23 ,
𝑎11 𝑎12 −𝑎13
𝑑1 = 𝑎31 𝑥3∗ ,
Δ = det (𝑎21 𝑎22 −𝑎23 ) ,
𝑎31 𝑎31 −𝑎33
𝑑2 = 𝑎32 𝑥3∗ ,
𝑟1 𝑎12 −𝑎13
𝑑3 = −𝑎33 𝑥3∗ ,
Δ 1 = det ( 𝑟2 𝑎22 −𝑎23 ) ,
−𝑟3 𝑎31 −𝑎33
𝑎11 𝑟1 −𝑎13
𝑑4 = 𝑎31 ,
𝑑5 = 𝑎32 ,
(3)
Δ 2 = det (𝑎21 𝑟2 −𝑎23 ) ,
𝑎31 −𝑟3 −𝑎33
𝑑6 = −𝑎33 .
The linearization of (6) near (0, 0, 0) is given by
𝑥̇ 1 (𝑡) = 𝑏1 𝑥1 (𝑡 − 𝜏) + 𝑏2 𝑥2 (𝑡) + 𝑏3 𝑥3 (𝑡) ,
𝑎11 𝑎12 𝑟1
Δ 3 = det (𝑎21 𝑎22 𝑟2 ) .
𝑥̇ 2 (𝑡) = 𝑐1 𝑥1 (𝑡) + 𝑐2 𝑥2 (𝑡 − 𝜏) + 𝑐3 𝑥3 ,
𝑎31 𝑎31 −𝑟3
Let 𝑥1 (𝑡) = 𝑥1 (𝑡) − 𝑥1∗ , 𝑥2 (𝑡) = 𝑥2 (𝑡) − 𝑥2∗ , and 𝑥3 (𝑡) = 𝑥3 (𝑡) −
𝑥3∗ and still denote 𝑥𝑖 (𝑡) (𝑖 = 1, 2, 3) by 𝑥𝑖 (𝑡) (𝑖 = 1, 2, 3), and
then (2) takes the form
𝑥̇ 1 (𝑡) = 𝑏1 𝑥1 (𝑡 − 𝜏) + 𝑏2 𝑥2 (𝑡) + 𝑏3 𝑥3 (𝑡)
𝑥̇ 3 (𝑡) = 𝑑1 𝑥1 (𝑡) + 𝑑2 𝑥2 (𝑡) + 𝑑3 𝑥3 (𝑡 − 𝜏) ,
whose characteristic equation takes the form
𝜆 − 𝑏1 𝑒−𝜆𝜏
det (
𝑥̇ 2 (𝑡) = 𝑐1 𝑥1 (𝑡) + 𝑐2 𝑥2 (𝑡 − 𝜏) + 𝑐3 𝑥3 + 𝑐4 𝑥1 (𝑡) 𝑥2 (𝑡)
+ 𝑐5 𝑥2 (𝑡) 𝑥2 (𝑡 − 𝜏) + 𝑐6 𝑥2 (𝑡) 𝑥3 (𝑡) ,
−𝑐1
−𝑏2
−𝑏3
𝜆 − 𝑐2 𝑒−𝜆𝜏
−𝑐3
−𝑑1
+ 𝑏4 𝑥1 (𝑡) 𝑥1 (𝑡 − 𝜏) + 𝑏5 𝑥1 (𝑡) 𝑥2 (𝑡)
+ 𝑏6 𝑥1 (𝑡) 𝑥3 (𝑡) ,
(6)
−𝑑2
) = 0.
(7)
−𝜆𝜏
𝜆 − 𝑑3 𝑒
That is,
𝜆3 + 𝑚1 𝜆 + 𝑚2 + (𝑚3 𝜆2 + 𝑚4 ) 𝑒−𝜆𝜏 + 𝑚5 𝜆𝑒−2𝜆𝜏
+ 𝑚6 𝑒−3𝜆𝜏 = 0,
(8)
Complexity
3
where
It follows from (14) that
𝑚1 = 𝑏2 𝑐1 + 𝑐3 𝑑2 − 𝑏3 𝑑1 ,
[𝑚2 cos 𝜔𝜏 − (𝑚1 𝜔 − 𝜔3 ) sin 𝜔𝜏 + 𝑚4
𝑚2 = −𝑏1 𝑐3 𝑑1 − 𝑏3 𝑑2 𝑐1 ,
𝑚3 = − (𝑏1 + 𝑐2 + 𝑑3 ) ,
𝑚4 = 𝑏3 𝑐2 𝑑1 − 𝑏2 𝑐1 𝑑3 − 𝑏1 𝑑2 𝑐3 ,
2
+ 𝑚5 𝜔 sin 𝜔𝜏] + [𝑚2 sin 𝜔𝜏 + (𝑚1 𝜔 − 𝜔3 ) cos 𝜔𝜏 (15)
(9)
𝑚5 = (𝑏2 + 𝑐2 ) 𝑑3 + 𝑏1 𝑐2 ,
According to sin 𝜔𝜏 = ±√1 − cos2 𝜔𝜏, then (15) takes the
form
𝑚6 = −𝑏1 𝑐2 𝑑3 .
Multiplying 𝑒𝜆𝜏 on both sides of (8), it is easy to obtain
(𝜆3 + 𝑚1 𝜆 + 𝑚2 ) 𝑒𝜆𝜏 + 𝑚3 𝜆2 + 𝑚4 + 𝑚5 𝜆𝑒−𝜆𝜏
+ 𝑚6 𝑒−2𝜆𝜏 = 0.
[𝑚2 cos 𝜔𝜏 − (𝑚1 𝜔 − 𝜔3 ) (±√1 − cos2 𝜔𝜏) + 𝑚4
(10)
We need the (...truncated)