بسم الله الرحمن الرحيم
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Transcript of بسم الله الرحمن الرحيم
بسم الله الرحمن الرحيم
رب علما ِوقل ًزدني
العظيم الله صدق
الباحثة رحاب نوري
On the dynamics of some Prey-predator
Models with Holling type-IV functional response
AbstractThis thesis deals with the dynamicalbehavior of prey-predator models with nonmonotonic functional response. Two
types of prey-predator models are proposed and studied.
The first proposed models consisting of Holling type-IV prey-predator model
involving intra-specific competition
However, the second proposed models consisting of Holling type-IV prey-predator model involving intra-specific competition in prey population with stage structure in
predator. Both the models are represented mathematically by nonlinear
differential equations. The existence, uniqueness and boundedness of the
solution of these two models are investigated. The local and global stability
conditions of all possible equilibrium points are established.
The occurrence of local bifurcation (such as saddle-node, transcritical and pitchfork) and Hopf bifurcation near each of the equilibrium points are discussed. Finally, numerical simulation is used to study the
global dynamics of both the models.
Chapter one
Preliminary
Mathematical model; is mathematical construct, often an
equation or a relation ship, designed to study the behavior of
a real phenomena.
Definition: Any group of individuals, usually of a single
species, occupying a given area at the same time is known as
population.
The application of mathematical method to problem in
ecology has resulted in a branch of ecology know as
mathematical ecology,.
There are three different kinds of interaction between any
given pair of species, these are described as bellow.
mutualisms or symbiosis (+,+), in which the existence of
each species effects positively on the growth of the other
species (i.e. increases in the first species causes
increases in the growth of the second species )
Competition (-,-), in which the existence of each species
effect negatively on the growth of the other species.
prey-predator (-,+) in which the existence of the first species
(prey) effects positively (increases) on the growth of the
second species (predator), while the existence of the
second species
(predator) effects negatively (decreases) on the growth
of the first species (prey).
Functional response; is that function, which refers to the
change in the density of prey attacked per unit at time per
predator as the prey density changes .the functional response
can be classified into three classes with respect to its
dependence on the prey or predator ,those are :
prey-dependent functions : the term prey-dependent means
that the consumption rate by each predator is a function of
prey density only, that is . In the following, the most
commonly used prey-dependant types functional reasons are
presented
)(),( xfyxf
(i) lotka-volterra type: in which the consumption rat of
individual predator increases linearly with prey. Hence the lotka
- volterra type of functional response can be written as follows:
Where is the consumption rate of prey by p rate of prey
by predator.
0;)( xaxxf0a (1)
(1)
2 4 6 8 10x value
20
40
60
80
100y
(ii) Holling type-I
In which the consumption rate of individual predator increases
lineally with prey density and when the predator satiate then it
becomes constant. Hence the Holling type-I functional
response can be written as follows:
Where is the value of prey density at which the predator
satiate at constant
x x0
)(
xxf
10 20 30 40x value
20
40
60
80
100y
(iii) Holling type-II: in which the consumption rate of individual
predator increases at a decreasing rate with prey density until it
becomes constant at satiation level. It is a hyperbola the
maximal value asymptotically, and defined by
Here is a search rate, h is the time spent on the
handling of one prey, is the maximum attack rate and b is
the half saturation level
2)( abf
ha 1
A
a
(3)xbax
AhxAxxf
1)(
2 4 6 8 10x value
0.5
1
1.5
2y
(iv) Holling type-III:
In this type of functional response the consumption rate of
individual predator accelerates at first and then decelerates
towards satiation level. It is defined as:
2
2
2
2
1)(
xbax
AhxAxxf
(4)
2 4 6 8 10x value
0.5
1
1.5
2
2.5
y
(V) Holling type-IV:
The type of functional response suggested by Andrews. The
Holling type IV functional response is of the form.
(5)
axixMxxf
2)(
2. Ratio-dependent function :
The prey-dependent functional responses do not
incorporate the predator abundance in it forms. Therefore,
Aridity and Ginsberg suggested using new type of functional
response called ratio-dependent, in which the rate of prey
consumption per predator depends not only on prey density
but instead depends on the ratio between the prey and
predator density. The Aridity -Ginsberg ratio dependent
response can be written as:
xbyax
AhxyAx
yxAh
yxA
yxf
1
),( (6)
3.predator-dependent functions;
In this type, the functional responses are depending on both
prey and predator densities. It is observed that high predator
density leads to more frequent encounters between
predators.
The most commonly used predator dependent functional
response is that proposed by DeAngalies and independently
by Beddingnon, which is now know as DeAnglis-Beddington
functional response:cxby
axAhxByAxyxf
1),(
(7)
The dynamics of Holling type IV prey predator model
with intra- specific competition
Chapter two
Mathematical models
Let x be the density of prey species at time ,y be the density
of predator species at time that consumes the prey species
according to Holling type IV functional response then the
dynamics of a prey–predator model can be represented by the
following system of ordinary differential equation.
t ttt
(8)
),(
),(
22
12
yxyfyxxxedy
dtdy
yxxfxxybxax
dtdx
with and Note that all the parameters of system
(8) are assumed to be positive constants and can be described
as follow:
is the intrinsic growth rate of the prey population; is the
intrinsic death rate of the predator population; the parameter
is the strength of intra-specific competition among the prey
species; the parameter can be interpreted as the half-
saturation constant in the absence of any inhibitory effect; the
parameter is a direct measure of the predator immunity from
the prey; is the maximum attack rate of the prey by a
predator; represents the conversion rate; and finally is the
strength of intra-specific competition among the predator
species .
0)0( x
aa
d
0)0( y
b
e
e
Now I worked on my research and I finished to finding and
proofing the following
1. Existence and Local Stability analysis of system (8) with
persistence
(1) The trivial equilibrium point always exists.
(2) The equilibrium point always
exists, as the prey population grows to the carrying capacity in
the absence of predation.
)0,0(0 E
0,1 baE
(3) There is no equilibrium point on as the predator
population dies in the absence of its prey.
(4) The positive equilibrium point exists in
the interior of the first quadrant if and only if there is a positive
solution to the following algebraic nonlinear equations:
We have the polynomial from five degrees
axisy
),( **2 yxE
0)( 012
23
34
45
5 AxAxAxAxAxAxf
And its exists under the condition, and when I
investigated varitional matrix for my system and
substitute we get the eigenvalues are
and Therefore, is locally
asymptotically stable if and only if
0,1 baE 01 ax
1Ebaba
abedy
21
dbaba
abe
22
While is saddle point provided that
And when I investigated varitional matrix for my system
and substitute we get is locally
asymptotically stable if and only if
and
)0,(1 baE
dbaba
abe
22
),( **2 yxE 2E
2*)*()*2(** Rybxxyx
RxyxeRb )2()( **2*223
And the persistence is proof by using the Gard and Hallam
method.
2.Global dynamical behavior of the system (8)
I proof the global dynamical behavior of system (8) and
investigated by using the Lyapunov method
3.The System(8) has a Hopf –bifurcation.
Near the positive equilibrium point at the parameter value
)*2(***)( 2*
*
xyxRbybx
4.The system (8) is uniformly bounded
In this section the global dynamics of system (8) is studied
numerically. The system (8) is solved numerically for different sets
of parameters and for different sets of initial condition, by using
six order Runge-Kutta method
5. Numerical analysis
0.01 0.75e 0.01d 1 0.75 0.50 0.2b 1
a
(8a)
2.5 3.5 4.5 5.5 6.51.5
2.5
3.5
4.5
(a)
x
y
initial point (3.0,3.0)
initial point (4.0,2.0)
initial point (6.0,3.0)
Stable point (4.71,3.99)
0 1 2 3 4 5
x 104
3
3.2
3.4
3.6
3.8
4
4.2
4.4
4.6
4.8b
Time
popu
latio
n
Fig1: (a) Globally asymptotically stable positive point of
system (8) for the data starting from (8a) with
different initial values. (b) Time series of the attractor
given by Fig 1(a)
3 3.5 4 4.5 50
0.5
1
1.5
2
2.5
3
a
Prey
Pre
dato
r
0 2 4 6 8 10
x 104
0
0.5
1
1.5
2
2.5
3
3.5
4
4.5
5
5.5b
Time
Pop
ulat
ion
Fig. 2: (a) The system (8) approaches asymptotically to
stable point 0,51 E with the data given in (8a)
05.0dwith starting from (3, 3), (b) Time series of the
attractor given by Fig1 (a).
0 1 2 3 4 50
2
4
6
8
10
12a
Prey
Pre
dato
r
initial point(3.0,3.0)
0 1 2 3 4 5 6 70
2
4
6
8
10
12b
Prey
Pre
dato
r
initial point(6.0,4.0)
0 2 4 6 8 10
x 104
0
2
4
6
8
10
12c
Time
popu
latio
n
0 2 4 6 8 10
x 104
0
2
4
6
8
10
12d
Time
Pop
ulat
ion
Fig2: Globally asymptotically stable limit cycle of system
(8) for the data given by Eq. (8a) with 75.0
(a) The solution approaches to limit cycle from inside
(b) The solution approaches to limit cycle from outside (c) Time series for Fig (1a) (d) Time series for Fig (1b).
Chapter three
Stability Analysis of a stage
structure
prey-predator model with
Holling type IV functional response
1.The mathematical models),,( 2112
2 yyxfxxybxax
dtdx
),,()( 21222
111 yyxf
xxxyeyDd
dtdy
),,( 2132212 yyxfydDydtdy
)9(
1.All the solutions of system (9) which initiate in 3
are uniformly bounded2. Existence and Local Stability analysis of system (9)
are investigate
(2a) The trivial equilibrium point always exists.(2b) It is well known that, the prey population grows
to the carrying capacity in the absence of ba
predator, while the predator population dies in the absence of the prey, then the axial
equilibrium point
0,0,1 baE always exists.
(3) There is no equilibrium point in the as the predator population dies in the
absence of its prey.(4) The positive equilibrium point ),,( *
2*1
*2 yyxE
exists in the 3. Int
Now we obtain the following third order polynomial
equation.
0012
23
3 BxBxBxB
4.The Bifurcation of system (9)the occurrence of a simple Hopf bifurcation and local
bifurcation (such as saddle node,pitck fork and a
transcritical bifurcation) near the equilibrium points of
system (9) are investigated.
3. Global dynamical behavior of system (9) are
investigatewith the help of Lyapunov function
5.Numerical analysis
In this section the global dynamics of system (9) is studied
numerically. The system (9) is solved numerically for
different sets of parameters and for different sets of initial
condition, by using six order Runge-Kutta method
0.05 0.35,e 0.25,D 0.01,d 2, 0.75, 1, 0.2,b ,25.0
21
da
(9a)
00.5
11.5
00.2
0.40.6
0.80
0.5
1
1.5
Prey
(a)
Immature Predator
Mat
ure
Pred
ator
Initial point(0.85,0.75,0.65)
Initial point(0.65,0.55,0.45)
Initial point(0.45,0.35,0.25)
Stable point(0.38,0.08,0.44)
0 0.5 1 1.5 2
x 105
0
0.4
0.8
1.2(b)
Time
Popu
latio
ns
Fig. (1): (a) The solution of system (9) approaches
asymptotically to the positive equilibrium point starting
from different initial values for the data given by Eq.
(9a). (b) Time series of the attractor in (a) starting at
(0.85, 0.75, 0.65).
01
23
0
0.5
10
1
2
Prey
(a)
Immature Predator
Mat
ure
Pred
ator
Initial point(0.85,0.75,0.65)
Initial point(0.85,0.75,0.65)
0 2.5 5 7.5
x 104
0
0.5
1
1.5
2
2.5(b)
Time
Popu
latio
ns
0 2.5 5 7.5
x 104
0
0.5
1
1.5
2
2.5(c)
Time
Popu
latio
ns
Fig. (2): (a) Globally asymptotically stable limit cycle
of system (9) starting from different initial values for
the data given by Eq. (9a) with
(c) Time series of the attractor in (a)
5.0a (b) Time series of the attractor in (a) starting at
(0.85, 0.75, 0.65).
(1.25, 0.25, 0.75).starting at
0 2 4 6 8
x 104
0
1
2
3
4
5
6
Time
Popu
latio
ns
Fig. (3): The trajectory of system (9) approaches
asymptotically to stable point 0,0,51 E for 1awith the rest of parameter as in Eq. (9a).