<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JAMP</journal-id><journal-title-group><journal-title>Journal of Applied Mathematics and Physics</journal-title></journal-title-group><issn pub-type="epub">2327-4352</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jamp.2016.412218</article-id><article-id pub-id-type="publisher-id">JAMP-73134</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  Stability, Chaos and Estimation of the Unknown Parameters of Habitat Destruction Model with Prey-Predator-Top Predator
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Saba</surname><given-names>Mohammed Alwan</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Omalsad</surname><given-names>Hamood Odhah</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Mathematics and Computer Science, College of Sciences, IBB University, Ibb, Yemen</addr-line></aff><aff id="aff2"><addr-line>Department of Mathematics, College of Sciences and Humanities, Prince Sattam Bin Abdulaziz University, Hotat Bany Tamim, Kingdom of Saudi Arabia</addr-line></aff><pub-date pub-type="epub"><day>05</day><month>12</month><year>2016</year></pub-date><volume>04</volume><issue>12</issue><fpage>2254</fpage><lpage>2271</lpage><history><date date-type="received"><day>November</day>	<month>19,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>December</month>	<year>26,</year>	</date><date date-type="accepted"><day>December</day>	<month>29,</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  This paper is devoted to study the problem of stability, chaos behavior and parameters estimation of the habitat destruction model with three-species (prey, predator and top-predator). The mathematical formula of the model and its proposed interactions are presented. Some important special solutions of systems are discussed. The stationary states of the model are derived. Local stability conditions for the stationary states are derived. Furthermore, the chaotic behavior of the model is discussed and presented graphically. Using Liapunov stability technique, the dynamic estimators of the unknown probabilities and their updating rules are derived. It is found that, the control laws are non-linear functions of the species densities. Numerical illustrative examples are carried out and presented graphically.
 
</p></abstract><kwd-group><kwd>Prey</kwd><kwd> Top-Predator</kwd><kwd> Three-Species</kwd><kwd> Estimation</kwd><kwd> Habitat Destruction</kwd><kwd> Lyapunov Function</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The habitat destruction is very important topic, which has received considerable attention in the last years. It is sure that there is a direct correlation between the preservation of the environment, human civilization and progress, and vice versa. Some believe that the chaos is behind each destruction in the environment. In contrast, the others believe that the chaos provides a chance or space for the great changes and developments. It’s for sure that, the chaos is one of the main causes of the environmental destruction, but it helps to achieve the needed balance in the environment. So, there is a controversy about whether the chaos has a positive role in the world or not. The balance of the environment comes also, from the natural and bounded coexistence between the organisms. The future of the habitat should have a great interest. There are some studies that have focused on this, for example see [<xref ref-type="bibr" rid="scirp.73134-ref1">1</xref>] .</p><p>When the habitat is no longer able to provide appropriate conditions for the life of its organisms, we can say that, the environment reached to the destruction stage, which is considered as an important factor causing extinction. It effects on various species not only directly but also indirectly. The accumulation of the destruction in a local area increases the risk of extinction in a bigger area and the increasing of the habitat destruction caused an imbalance in the densities of the populations of prey and predator. So, we can say that, the causal relation between species extinction and the habitat destruction is very complicated [<xref ref-type="bibr" rid="scirp.73134-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.73134-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.73134-ref4">4</xref>] .</p><p>The variation of the total population size is determined by birth and the mortality rates [<xref ref-type="bibr" rid="scirp.73134-ref5">5</xref>] . In a closed population (i.e., no immigration) of size N, the change in population size for a change in time is given by<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x2.png" xlink:type="simple"/></inline-formula>, where b, d and l = b − d are the birth, death and the growth rates per individual respectively. It is clearly that if l &gt; 0, the population grows; if l &lt; 0, the population heading towards extinction; if l = 0, no change in the population size. Recent models of competition indicate that, the effect of habitat destruction on coexisting between preys and predators is dependent on the ratio of extinction risk due to predation and prey colonization rate [<xref ref-type="bibr" rid="scirp.73134-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.73134-ref7">7</xref>] .</p><p>A lattice model represents the motion of a network of particles, where the motion is produced by forces acting between the neighboring particles. Lattice models also are used to simulate the structure of polymers and can exhibit its dynamic behaviors. Mathematically, the motion is governed by a system of ordinary differential equations. The behavior of the particles depends on the precise nature of the interaction. The main problems which have been treated involve the long time behavior of the system [<xref ref-type="bibr" rid="scirp.73134-ref8">8</xref>] .</p><p>The results of this study are extend to the results that introduced by [<xref ref-type="bibr" rid="scirp.73134-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.73134-ref3">3</xref>] where it found that the increase of habitat destruction leads to reduction in the chance of coexistence of prey and predator, different patterns of extinction for the species (prey, predator and top predator), and decrease in the oscillations in the densities of both species (prey and predator). Also, this study is considered as a complement for the results of the study [<xref ref-type="bibr" rid="scirp.73134-ref9">9</xref>] that concentrates on two-Species model, (prey-predator) which found that the system in general is unstable. In other hands, the chaotic behavior of the uncontrolled system has seemed clear through the graphs of its limit cycles and some attractors. The dynamic estimators of the unknown parameters and its updating rules over time are derived from the conditions of the asymptotic stability of the system around its steady states.</p><p>Al-Mahdi and Khirallah have studied stability and bifurcation analysis of a model of cancer [<xref ref-type="bibr" rid="scirp.73134-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.73134-ref11">11</xref>] . Alwan has studied the stability and behavior for the model of stochastic lattice gas of prey-predator model with pair-approximation. She found that this system has a chaos behavior and she has derived the estimators of the unknown parameters and the updating [<xref ref-type="bibr" rid="scirp.73134-ref12">12</xref>]</p><p>The considered system contains three-species, which including prey, predator and top-predator. The assumed interactions and mathematical form of this model will be presented. Some special solutions of this system will be discussed. Chaos and linear stability will be studied. The dynamic estimators of the unknown parameters of this model and its updating rules will be calculated.</p><p>This paper has the following structure. In Section 2, the lattice model and its assumed interactions are discussed and presented graphically. The mathematical formula model will be presented. Section 3 is devoted to study the chaos and linear stability analysis of the system. In Section 4, it is the analysis of some special solutions. Estimation of the unknown parameters and the updating rules are derived in Section 5. In Section 6, numerical solutions are derived and presented graphically. Finally, Conclusions are provided in Section 7.</p></sec><sec id="s2"><title>2. The Lattice Model</title><p>In this section, the assumed interactions of the proposed model will be discussed and the mathematical formula will be presented.</p><p>Each site in the lattice can be labeled by X, Y, Z or O, where X, (or Y, Z) is the site occupied by prey (or predators), and O represents the vacant site. The assumed interactions of this model are given by [<xref ref-type="bibr" rid="scirp.73134-ref2">2</xref>] :</p><disp-formula id="scirp.73134-formula25"><label>(1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x3.png"  xlink:type="simple"/></disp-formula><p>The above interactions respectively represent two kinds of predation with probability 1, reproduction of prey with probability r<sub>0</sub> and the deaths of the three-species prey, predator and top-predator, with probabilities r<sub>1</sub>, r<sub>2</sub>, r<sub>3</sub> respectively. The transition matrix that presents the previous processes can be written as the following:</p><disp-formula id="scirp.73134-formula26"><graphic  xlink:href="http://html.scirp.org/file/10-1720748x4.png"  xlink:type="simple"/></disp-formula><p>Also, these interactions can be represented by <xref ref-type="fig" rid="fig1">Figure 1</xref>. In the lattice boundary, the barriers are putting as a link between neighboring sites probability p. which called barrier density. The interactions (1.1), (1.2) and (1.3) are assumed occur between neighboring lattice points as presented in <xref ref-type="fig" rid="fig1">Figure 1</xref>.</p><p>Percolation is the case when the largest set of connected barriers encompasses the entire system. The local habitat destruction is shown when p takes a value near unity, almost all barriers are connected (Percolation case). The probability of the percolation takes a nonzero value when p exceeds a critical point p<sub>c</sub>. This value is assumed to be</p><fig-group id="fig1"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> The assumed transitions of the habitat destruction model of three-species.</title></caption><fig id ="fig1_1"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/10-1720748x5.png"/></fig><fig id ="fig1_2"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/10-1720748x6.png"/></fig></fig-group><p>p<sub>c</sub> = 0.5 [<xref ref-type="bibr" rid="scirp.73134-ref1">1</xref>] . In contrast, when p takes an extremely small value, no barriers may connect with each other. Thus, p can be used as measures of the intensity of habitat destruction.</p>The Mathematical Formula of the Model<p>The population dynamics of three-species model is described by the mean-field theory (MFT) [<xref ref-type="bibr" rid="scirp.73134-ref2">2</xref>] , as the following form:</p><disp-formula id="scirp.73134-formula27"><label>(2.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x7.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula28"><label>(2.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x8.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula29"><label>(2.3)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x9.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula30"><label>(2.4)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x10.png"  xlink:type="simple"/></disp-formula><p>where the dot represents the derivative with respect to time, P<sub>0</sub>, P<sub>1</sub>, P<sub>2</sub> and P<sub>3</sub> are the densities of O, X, Y and Z respectively, r<sub>i</sub>, i = 0, 1, 2, 3 are four unknown probabilities, which represent the probabilities of reproduction of prey, deaths of the prey, predator and top-predator, respectively. The probability p takes a non-critical value as explained previously.</p><p>The state variables of this system are subject to the following relationship</p><disp-formula id="scirp.73134-formula31"><label>(3)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x11.png"  xlink:type="simple"/></disp-formula><p>Therefore, for simplicity in our study, one can take just three equations instead of four, which are considered sufficient to demonstrate the chaotic behavior of the system and to estimate the unknown probabilities. Accordingly, using the relation in Equation (3), one can reduce the model in Equations (2) to the following model:</p><disp-formula id="scirp.73134-formula32"><label>(4.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x12.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula33"><label>(4.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x13.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula34"><label>(4.3)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x14.png"  xlink:type="simple"/></disp-formula></sec><sec id="s3"><title>3. Chaos and Linear Stability Analysis</title><p>This section is devoted to study the local stability and the chaos behavior near the steady states of the three-spice model in Equations (4). The stationary states of the system in Equations (4) will be derived. The biological conditions for these steady states will be discussed. In addition, the instability conditions will be derived. Furthermore, some numerical solutions for the uncontrolled system and its instability, chaotic behavior and different attractors will be presented graphically.</p><sec id="s3_1"><title>3.1. The Stationary States</title><p>In this subsection, the stationary states will be derived the biologically conditions will be discussed. The stability study of the stationary states will be discussed later.</p><p>The stationary probabilities of the three-species model in Equations (4) can be obtained by setting the following simultaneous equations</p><disp-formula id="scirp.73134-formula35"><label>(5)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x15.png"  xlink:type="simple"/></disp-formula><p>By solving this system analytically one can see the following stationary states.</p><p>a) The first stationary probability of the system in Equations (4) is given by:</p><disp-formula id="scirp.73134-formula36"><label>(6)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x16.png"  xlink:type="simple"/></disp-formula><p>This solution corresponds to a vacuum-absorbing state.</p><p>b) The second stationary probability of the system is given by:</p><disp-formula id="scirp.73134-formula37"><label>(7)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x17.png"  xlink:type="simple"/></disp-formula><p>Clearly, the density of the top-predator in this solution is negative. Due to that, this solution is biologically inadmissible.</p><p>c) The third stationary probability of the system is</p><disp-formula id="scirp.73134-formula38"><label>(8)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x18.png"  xlink:type="simple"/></disp-formula><p>where</p><disp-formula id="scirp.73134-formula39"><label>(9)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x19.png"  xlink:type="simple"/></disp-formula><p>The necessary condition for solution in Equation (8) to be biologically admissible is</p><disp-formula id="scirp.73134-formula40"><label>(10)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x20.png"  xlink:type="simple"/></disp-formula><p>d) The fourth stationary probability of the system (4) is given by:</p><disp-formula id="scirp.73134-formula41"><label>(11)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x21.png"  xlink:type="simple"/></disp-formula><p>The necessary condition for this solution to be biologically admissible is</p><disp-formula id="scirp.73134-formula42"><graphic  xlink:href="http://html.scirp.org/file/10-1720748x22.png"  xlink:type="simple"/></disp-formula><p>e) The fifth stationary probability of the system (4) is given by:</p><disp-formula id="scirp.73134-formula43"><label>(12)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x23.png"  xlink:type="simple"/></disp-formula><p>The necessary condition for this solution to be biologically admissible is</p><disp-formula id="scirp.73134-formula44"><label>(13)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x24.png"  xlink:type="simple"/></disp-formula><p>It is worth mentioning that, the condition in (13) is a sufficient condition to be S<sub>4</sub> and S<sub>3</sub> be biologically admissible because</p><disp-formula id="scirp.73134-formula45"><graphic  xlink:href="http://html.scirp.org/file/10-1720748x25.png"  xlink:type="simple"/></disp-formula></sec><sec id="s3_2"><title>3.2. Linear Stability Analysis</title><p>In this subsection, we will discuss the stability analysis of the three-species model in Equations (4) near its steady states. We will calculate the Jacobian matrix of the system at its steady states and calculate the eigenvalues corresponding to each steady state. Then, we will determine whether these eigenvalues contain at least a positive root as a sufficient condition for instability [<xref ref-type="bibr" rid="scirp.73134-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.73134-ref14">14</xref>] . Also, we will seek to determine the instability conditions for each steady state if needed.</p><p>The Jacobian matrix <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x26.png" xlink:type="simple"/></inline-formula> of the system in Equation (4) evaluated at the steady state <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x26.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x27.png" xlink:type="simple"/></inline-formula> is given by:</p><disp-formula id="scirp.73134-formula46"><label>(14)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x28.png"  xlink:type="simple"/></disp-formula><p>Now let’s start by examining the instability of the steady states <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x29.png" xlink:type="simple"/></inline-formula> of three-species model.</p><p>・ The eigenvalues of the Jacobian matrix evaluated at S<sub>1</sub> are given by</p><disp-formula id="scirp.73134-formula47"><label>(15)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x30.png"  xlink:type="simple"/></disp-formula><p>Clearly, S<sub>1</sub> is unstable if<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x31.png" xlink:type="simple"/></inline-formula>. The steady state S<sub>1</sub> needs further stability analysis if<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x31.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x32.png" xlink:type="simple"/></inline-formula>, because in this situation, we will get a critical case.</p><p>・ The eigenvalues of the Jacobian matrix evaluated at S<sub>2</sub> are given by solving the characteristic equation, which is</p><disp-formula id="scirp.73134-formula48"><label>(16)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x33.png"  xlink:type="simple"/></disp-formula><p>Therefore, the eigenvalues of <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x34.png" xlink:type="simple"/></inline-formula> are the roots of Equation (16) which are given by</p><disp-formula id="scirp.73134-formula49"><label>(17)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x35.png"  xlink:type="simple"/></disp-formula><p>Due to the existence of a positive root in (17), the steady state S<sub>2</sub> is absolutely unstable.</p><p>・ The eigenvalues of the Jacobian matrix evaluated at S<sub>3</sub> are given by</p><disp-formula id="scirp.73134-formula50"><label>(18)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x36.png"  xlink:type="simple"/></disp-formula><p>For this steady state, if<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x37.png" xlink:type="simple"/></inline-formula>, then<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x37.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x38.png" xlink:type="simple"/></inline-formula>, which is a sufficient condition for instability of S<sub>3</sub>. but, this condition makes the prey density in S<sub>3</sub> has a negative value, therefore this condition is biologically, not admissible. On other hand, if<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x37.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x38.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x39.png" xlink:type="simple"/></inline-formula>, then<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x37.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x38.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x39.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x40.png" xlink:type="simple"/></inline-formula>. Therefore, this is a sufficient condition in order to be S<sub>3</sub> unstable.</p><p>・ The eigenvalues of the Jacobian matrix evaluated at S<sub>4</sub> are given by the roots of the following characteristic equation:</p><disp-formula id="scirp.73134-formula51"><label>(19)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x41.png"  xlink:type="simple"/></disp-formula><p>where</p><disp-formula id="scirp.73134-formula52"><label>(20)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x42.png"  xlink:type="simple"/></disp-formula><p>For the linear factor, the necessary condition for its root to be positive value is</p><disp-formula id="scirp.73134-formula53"><label>(21)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x43.png"  xlink:type="simple"/></disp-formula><p>This condition is sufficient for S<sub>4</sub> to be unstable.</p><p>It is worth mentioning, for the quadratic polynomial in Equation (19), the second coefficient <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x44.png" xlink:type="simple"/></inline-formula> is positive because of <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x44.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x45.png" xlink:type="simple"/></inline-formula> and<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x44.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x45.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x46.png" xlink:type="simple"/></inline-formula>. Also, the third coefficient is positive under the condition in (21). Since all the real coefficients of the quadratic polynomial in Equation (19) are positive, using the Routh’s stability criterion [<xref ref-type="bibr" rid="scirp.73134-ref15">15</xref>] , then all the roots of quadratic polynomial are negative if the condition (21) is satisfied. Accordingly, S<sub>4</sub> is unstable under the condition in (21) and the stability decision needs further stability analysis</p><p>・ The eigenvalues of the Jacobian matrix evaluated at S<sub>5</sub> are given by the roots of the following characteristic equation.</p><disp-formula id="scirp.73134-formula54"><label>(22)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x47.png"  xlink:type="simple"/></disp-formula><p>where</p><disp-formula id="scirp.73134-formula55"><label>(23)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x48.png"  xlink:type="simple"/></disp-formula><p>Without solving the polynomial between the rectangular brackets in (22) and using Descartes rule of signs to determine the number of positive zeros of the polynomial, one can find that, the first coefficient is positive, and by simple calculation, it is easy to see that if</p><disp-formula id="scirp.73134-formula56"><label>(24)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x49.png"  xlink:type="simple"/></disp-formula><p>then,<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x50.png" xlink:type="simple"/></inline-formula>; and<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x50.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x51.png" xlink:type="simple"/></inline-formula>. Under this condition, the second coefficient of the polynomial between the rectangular brackets in Equation (23) will be positive and the third will be negative. In this case the polynomial has one variation in sign. Therefore, the polynomial has one positive real zeros and the other is negative. So, we can conclude that, S<sub>5</sub> is unstable if the condition in (24) is satisfied.</p><p>In the following we will present graphically, the system behavior over time, which illustrate the oscillatory behavior of the system.</p><p>In this figure, all state variables of the uncontrolled system in Equations (4) that appear in (a, b, c) have an oscillatory behavior. For limit cycles that appear in (d, e, f), all the neighboring trajectories tend to a limit-cycle at time tends to infinity, causing the so-called a stable limit-cycle, which indicates that the system has an oscillatory behavior.</p><p>In the following we will present a special behavior of this system which is a periodic orbits which called attractors as in <xref ref-type="fig" rid="fig3">Figure 3</xref>. Attractors is a special behavior, which generated by the dynamical system and steadily developing as long as there is no barrier</p><p>All graphs of uncontrolled densities, limit cycles and attractors in <xref ref-type="fig" rid="fig2">Figure 2</xref> and <xref ref-type="fig" rid="fig3">Figure 3</xref> well agree with the previous linear stability analysis that indicates that the habitat destruction model with three-species has a high chaotic behavior.</p></sec></sec><sec id="s4"><title>4. Analysis of Some Special Solutions</title><p>In this section, we will discuss some special solutions for this model, which give us a clearer perception for this mode. In addition, the absence of one or more of the components of the system has impact on the behavior of the system.</p><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> The uncontrolled densities of habitat destruction of three-species model and its limit cycles for the probabilities r<sub>0</sub> = 0.5, r<sub>1</sub> = 0.01, r<sub>2</sub> = 0.15, r<sub>3</sub> = 0.4 and the barrier density p = 0.3 and the initial densities <img data-original="http://html.scirp.org/file/10-1720748x53.png" /></title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/10-1720748x52.png"/></fig><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Different attractors of the habitat destruction model of the three-species for the following rates, parameters and initial densities</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/10-1720748x54.png"/></fig><p>・ The first special solution occurs when both prey and predator are absent, that is P<sub>1</sub> = 0 and P<sub>2</sub> = 0. In this case, the top-predator decreases exponentially with rate r<sub>3</sub> as indicants in the following growth equation:</p><disp-formula id="scirp.73134-formula57"><label>(25)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x63.png"  xlink:type="simple"/></disp-formula><p>In <xref ref-type="fig" rid="fig4">Figure 4</xref>, the top predator density decreases over time and converges to zero and the empty site density increases over time and converges to one as t converges to infinity. This situation represents a vacuum-absorbing state.</p><fig id="fig4"  position="float"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> Simultaneous evanescence and growth of top-predator and empty sites respectively in the absence case of prey and predator at <img data-original="http://html.scirp.org/file/10-1720748x65.png" /></title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/10-1720748x64.png"/></fig><p>・ The second special solution occurs in the absence of both prey and predator, that is P<sub>1</sub> = 0 and P<sub>3</sub> = 0. This situation is similar to the previous case, therefore, the predator will be decreased exponentially with rate r<sub>2</sub>, and the empty sites density increases over time to tend to one. This situation represents also, a vacuum-absorbing state.</p><p>・ Another special solution occurs when both of the predator and top-predator are absent, that is P<sub>2</sub> = 0 and P<sub>3</sub> = 0. In this case the model in Equation (4) will be reduced to the contact percolation process [<xref ref-type="bibr" rid="scirp.73134-ref2">2</xref>] , that is a one-species model we have where the birth and death processes of species X are assumed, which can be presented as <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x66.png" xlink:type="simple"/></inline-formula> and<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x66.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x67.png" xlink:type="simple"/></inline-formula>. In this case the system will take the following reducing form</p><disp-formula id="scirp.73134-formula58"><label>(26.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x68.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula59"><label>(26.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x69.png"  xlink:type="simple"/></disp-formula><p>By solving this system, we will take the following prey population growth:</p><disp-formula id="scirp.73134-formula60"><label>(27)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x70.png"  xlink:type="simple"/></disp-formula><p>where</p><disp-formula id="scirp.73134-formula61"><label>(28)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x71.png"  xlink:type="simple"/></disp-formula><p>Equation (27) indicates that, the density of the prey tends to <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x72.png" xlink:type="simple"/></inline-formula> as t tends to infinity. If the death probability of the prey be zero, then the prey population has a logistic growth and all sites of the lattice will be occupied by prey as t tends to infinity [<xref ref-type="bibr" rid="scirp.73134-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.73134-ref17">17</xref>] to make a prey-absorbing state as shown in <xref ref-type="fig" rid="fig5">Figure 5</xref>.</p><p>It is useful to notice that, in order the result in (27) be biologically admissible, the following condition must be satisfied:</p><disp-formula id="scirp.73134-formula62"><label>(29)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x73.png"  xlink:type="simple"/></disp-formula><p>・ Other special solution occurs when the top-predator only, is absent, that is P<sub>3</sub> = 0. Clearly, in this case the system in Equations (4) will be reduced to the subsystem of two-species (Prey-Predator) model,</p><fig id="fig5"  position="float"><label><xref ref-type="fig" rid="fig5">Figure 5</xref></label><caption><title> Simultaneous growth of both of prey and empty densities in the absence case of predator at<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x75.png" xlink:type="simple"/></inline-formula></title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/10-1720748x74.png"/></fig><disp-formula id="scirp.73134-formula63"><label>(30.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x76.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula64"><label>(30.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x77.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula65"><label>(30.3)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x78.png"  xlink:type="simple"/></disp-formula><p>which has been studied in [<xref ref-type="bibr" rid="scirp.73134-ref9">9</xref>] . It is found that, one absorbing stationary state and two active stationary states. It is found also that, these stationary states are unstable. Furthermore, this system showed a chaotic behavior.</p><p>・ In the absence of prey, P<sub>1</sub> = 0, we will obtain another two-species model (predator- top predator) as given below</p><disp-formula id="scirp.73134-formula66"><label>(31.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x79.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula67"><label>(31.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x80.png"  xlink:type="simple"/></disp-formula><p>This subsystem has two steady states, which are</p><disp-formula id="scirp.73134-formula68"><label>(32)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x81.png"  xlink:type="simple"/></disp-formula><p>The Jacobian matrix Jsub1 of the subsystem (31) evaluated at the steady sate <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x82.png" xlink:type="simple"/></inline-formula> is given by:</p><disp-formula id="scirp.73134-formula69"><label>(33)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x83.png"  xlink:type="simple"/></disp-formula><p>The Jacobian matrices Jsub11 and Jsub12 at e<sub>11</sub> and e<sub>12</sub> respectively, are given below</p><disp-formula id="scirp.73134-formula70"><label>(34)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x84.png"  xlink:type="simple"/></disp-formula><p>The eigenvalues of Jsub11 are</p><disp-formula id="scirp.73134-formula71"><label>(35)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x85.png"  xlink:type="simple"/></disp-formula><p>The eigenvalues of Jsub12 are</p><disp-formula id="scirp.73134-formula72"><label>(36)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x86.png"  xlink:type="simple"/></disp-formula><p>Clearly, the steady state e<sub>11</sub> is stable, while the steady state e<sub>12</sub> is absolutely unstable. Therefore, the subsystem (31) is unstable at least in one dimension.</p><p>・ The following considered special solution occurs when the predator is absent, that is P<sub>2</sub> = 0 In this case, the three-species system will be reduced to a subsystem of two- species model with prey-top predator as will present below</p><disp-formula id="scirp.73134-formula73"><label>(37.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x87.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula74"><label>(37.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x88.png"  xlink:type="simple"/></disp-formula><p>This system has the following two stationary solutions:</p><disp-formula id="scirp.73134-formula75"><label>(38)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x89.png"  xlink:type="simple"/></disp-formula><p>The Jacobian matrix Jsub2 of the subsystem in Equation (37) evaluated at its steady states <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x90.png" xlink:type="simple"/></inline-formula> is given by:</p><disp-formula id="scirp.73134-formula76"><label>(39)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x91.png"  xlink:type="simple"/></disp-formula><p>Therefore, the Jacobian matrices at e<sub>21</sub> and e<sub>22</sub> respectively, are given by:</p><disp-formula id="scirp.73134-formula77"><label>(40)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x92.png"  xlink:type="simple"/></disp-formula><p>and the eigenvalues of <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x93.png" xlink:type="simple"/></inline-formula> are:</p><disp-formula id="scirp.73134-formula78"><label>(41)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x94.png"  xlink:type="simple"/></disp-formula><p>and the eigenvalues of <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x95.png" xlink:type="simple"/></inline-formula> are:</p><disp-formula id="scirp.73134-formula79"><label>(42)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x96.png"  xlink:type="simple"/></disp-formula><p>Clearly, the steady state <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x97.png" xlink:type="simple"/></inline-formula> is unstable if <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x97.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x98.png" xlink:type="simple"/></inline-formula> and stable if <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x97.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x98.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x99.png" xlink:type="simple"/></inline-formula> and the stability decision needs more stability analysis if<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x97.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x98.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x99.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x100.png" xlink:type="simple"/></inline-formula>, in which one get a critical case. One can conclude that the subsystem (37) is unstable at least in one direction.</p><p>・ The last special solution occurs when no vacant sites in the lattice, that is P<sub>0</sub> = 0. In this case the processes: reproduction of prey, death of prey and death of predator will be disabled, and only the predation process will be remained. As a result of this, the density of predator has the following form</p><disp-formula id="scirp.73134-formula80"><label>(43)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x101.png"  xlink:type="simple"/></disp-formula><p>Equation (43) shows that, the predator population has a logistic growth and its density converges to one as t converges to infinity, in the same time the prey density converges to zero as t converges to infinity as shown in <xref ref-type="fig" rid="fig6">Figure 6</xref>. Therefore all the lattice sites will be occupied by predators to make a predator-absorbing state and the preys will be extinct.</p><fig id="fig6"  position="float"><label><xref ref-type="fig" rid="fig6">Figure 6</xref></label><caption><title> Simultaneous growth of the predator site density and the prey site density in the absence of empty sites at the initial value<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x103.png" xlink:type="simple"/></inline-formula></title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/10-1720748x102.png"/></fig></sec><sec id="s5"><title>5. Estimations of the Unknown Probabilities</title><p>This section is devoted to derive the estimators of the unknown probabilities of the three-species model of habitat destruction (4). The dynamic estimators of the unknown probability r<sub>i</sub>, i = 0, 1, 2, 3 and its updating rules will be calculated from the conditions of the asymptotic stability of the system (4) near its stationary solutions S<sub>k</sub>, k = 1, 2, ∙∙∙, 5 with assistance of some feedback variables e<sub>1</sub>, e<sub>2</sub> and e<sub>3</sub>.</p><p>At the beginning, we will develop the mathematical formula of the habitat destruction model of three-species with unknown probabilities in (4) to become as follows:</p><disp-formula id="scirp.73134-formula81"><label>(44.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x104.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula82"><label>(44.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x105.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula83"><label>(44.3)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x106.png"  xlink:type="simple"/></disp-formula><p>where <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x107.png" xlink:type="simple"/></inline-formula> are the estimators of the unknown probabilities r<sub>i</sub>, i = 0, 1, 2, 3 of the system (4). The model in Equations (44) has unstable stationary solution if<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x107.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x108.png" xlink:type="simple"/></inline-formula>. This solution is given by</p><disp-formula id="scirp.73134-formula84"><label>(45)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x109.png"  xlink:type="simple"/></disp-formula><p>The problem now is equivalent to stabilizing of these steady states and determining the updating rules <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x110.png" xlink:type="simple"/></inline-formula> of the estimators <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x110.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x111.png" xlink:type="simple"/></inline-formula> of the system unknown probabilities <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x110.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x111.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x112.png" xlink:type="simple"/></inline-formula> with help of the controllers<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x110.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x111.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x112.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x113.png" xlink:type="simple"/></inline-formula>.</p><p>The Lyapunov function of the system (4) that will be used can be considered as the following positive definite form</p><disp-formula id="scirp.73134-formula85"><label>(46)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x114.png"  xlink:type="simple"/></disp-formula><p>and its time derivative is given by</p><disp-formula id="scirp.73134-formula86"><label>(47)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x115.png"  xlink:type="simple"/></disp-formula><p>By choosing the controllers as follows:</p><disp-formula id="scirp.73134-formula87"><label>(48.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x116.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula88"><label>(48.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x117.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula89"><label>(48.3)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x118.png"  xlink:type="simple"/></disp-formula><p>and by substituting (48) in (47), one can get that the appropriate choice for the updating rules <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x119.png" xlink:type="simple"/></inline-formula> for <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x119.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x120.png" xlink:type="simple"/></inline-formula> to be a negative definite function are given by</p><disp-formula id="scirp.73134-formula90"><label>(49.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x121.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula91"><label>(49.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x122.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula92"><label>(49.3)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x123.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula93"><label>(49.4)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x124.png"  xlink:type="simple"/></disp-formula><p>where <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x125.png" xlink:type="simple"/></inline-formula> and <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x125.png" xlink:type="simple"/></inline-formula><inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x126.png" xlink:type="simple"/></inline-formula> are non-negative control constants.</p><p>By substituting the choices (48) and (49) in (47), <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x127.png" xlink:type="simple"/></inline-formula>will be a negative definite function, which proves the asymptotic stability of the solution (45) in Lyapunov sense. Further that, this solution is globally asymptotically stable since V is radially unbounded [<xref ref-type="bibr" rid="scirp.73134-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.73134-ref19">19</xref>] . And by substituting Equation (48) in the controlled system in Equation (44), in addition Equation (9) we get the following closed system of nonlinear deferential equations following form:</p><disp-formula id="scirp.73134-formula94"><label>(50.1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x128.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula95"><label>(50.2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x129.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula96"><label>(50.3)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x130.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula97"><label>(50.4)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x131.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula98"><label>(50.5)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x132.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula99"><label>(50.6)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x133.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.73134-formula100"><label>(50.7)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/10-1720748x134.png"  xlink:type="simple"/></disp-formula><p>This system can be used to study the dynamics of the habitat destruction model of three-species with unknown probabilities. Since this system is nonlinear, its solution will be numerical as will be seen bellow.</p></sec><sec id="s6"><title>6. Numerical Solution</title><p>This section presents numerical solution of the controlled nonlinear system of the habitat destruction model with prey-predator-top-predator, and the estimators of the system unknown probabilities to show how the control for this system is possible. Also, numerical examples for controlled model are carried out for various probabilities values and different initial densities. A numerical solution is presented below</p><p><xref ref-type="fig" rid="fig7">Figure 7</xref> indicates that the controlled densities of the three species converge to the steady state over time. The steady states are presented by the dotted lines.</p><p>For the same values of probabilities, parameters and initial densities above, let us represent the estimators of the unknown probabilities.</p><p>In <xref ref-type="fig" rid="fig8">Figure 8</xref>, it is shown that, the estimators <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x142.png" xlink:type="simple"/></inline-formula> converge to the assumed real values r<sub>i</sub> over time, where the assumed real values are represented by the dotted</p><fig id="fig7"  position="float"><label><xref ref-type="fig" rid="fig7">Figure 7</xref></label><caption><title> The controlled densities of (a) prey, (b) predator, and (c) top-predator sites of the habitat destruction model of three-species for the following values of probabilities, parameters and initial densities</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/10-1720748x143.png"/></fig><fig id="fig8"  position="float"><label><xref ref-type="fig" rid="fig8">Figure 8</xref></label><caption><title> The estimator <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/10-1720748x145.png" xlink:type="simple"/></inline-formula> of the unknown probabilities r<sub>i</sub>, i = 0, 1, 2, 3 of the three-species model of the habitat destruction system with three-species prey, predator and top-predator</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/10-1720748x144.png"/></fig><p>lines. It is necessary to know that the very small differences between the assumed real values and the estimated values are be due to the necessary approximations in the numerical method of solution.</p></sec><sec id="s7"><title>7. Conclusions</title><p>This paper is devoted to study the linear stability, chaos and estimation of the unknown parameters of the habitat destruction model with prey-predator and top-predator. Using the linear stability analysis, it is found that, this system has a high chaotic behavior. The dynamic estimators of the unknown parameters and its updating rules over time are derived from the conditions of the asymptotic stability of the system around its steady states. The controller laws are found as non-linear functions of the species densities. Numerical examples for the controlled system are carried out and presented graphically.</p><p>The chaotic behavior of this system gives us a reason to study the optimal control for this system in future.</p></sec><sec id="s8"><title>Cite this paper</title><p>Alwan, S.M. and Odhah, O.H. (2016) Stability, Chaos and Esti- mation of the Unknown Parameters of Habitat Destruction Model with Prey-Predator- Top Predator. Journal of Applied Mathematics and Physics, 4, 2254-2271. http://dx.doi.org/10.4236/jamp.2016.412218</p></sec></body><back><ref-list><title>References</title><ref id="scirp.73134-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Ergazaki, M. and Ampatzidis, G. (2012) Students’ Reasoning about the Future of Disturbed or Protected Ecosystems &amp; the Idea of the “Balance of Nature”. 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