The Dynamics Of Modified Leslie-Gower The Pest- Predator System With .

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Advances in Engineering Research, volume 209International Joint Conference on Science and Engineering 2021 (IJCSE 2021)The Dynamics of Modified Leslie-Gower the PestPredator System with Additional Food and Fear EffectDian Savitri1,* Abadi2 Manuharawati3 Muhammad Jakfar41,2,3,4Departement of Mathematics, Universitas Negeri Surabaya, Surabaya, IndonesiaCorresponding author. Email: diansavitri@unesa.ac.id*ABSTRACTWe have studied a dynamic analysis of the prey-predator model that describes the interaction between pests andpredators as natural enemies. The model is considering a Modified Leslie-Gower prey-predator model with the natureof fear of the growth of pests and additional food to predator. The predation uses the Holling type II response functionby assuming that the predator also needs additional food to survive. We analyze the dynamics of the system includesdetermining the equilibrium point as well as local stability analysis. It shows that there are four equilibriums in whicheach equilibrium point exists and three equilibrium points are local asymptotically stable with some sufficientconditions. Numerical simulations were carried out to support the analytical finding. The numerical simulations alsoindicate that bifurcation occurs and the possible phase portraits diagram has been depicted. The simulation results anddiscussion of the diagram bifurcation are lucidly presented in the text of the paper.Keywords: Dynamics, Pest-predator, Stability, Bifurcation.1. INTRODUCTIONRice is the main food crop grown by farmers inIndonesia. The growth of rice plants in Indonesia is at riskin the form of pest and disease attacks. The main pests ofrice plants in Indonesia are field mice. The increasing ratpopulation is a problem for farmers. Rat pest control isan effort to reduce the rat population level as low aspossible so that economically the presence of rat pests isnot detrimental [1]. Pests have natural enemies in theform of predators. Natural enemies are used tocontrolling the number of pest populations naturally sothat the ecosystem remains stable [2]. The population ofowls as a natural enemy is causing fear in rat pests [3]. Ahigh level of fear in rat pests caused by predators resultsin reduced reproduction of rats so that it can reduce thenumber of rat pests. The reduction in the number of ratpests makes predators look for alternative food other thanrats. Additional food is needed to keep predatory speciesfrom becoming extinct so that the balance of the twopopulations is controlled.Based on the problem of pest growth, it can be appliedto a mathematical model of the interaction of two species.The model describes the dynamics of the spread of pestsand natural enemies, namely predators. The pest-predatormodel considers predation and the nature of the pestagainst predators. Some scientists are interested indeveloping a similar model with various assumptions.Srinivasu [4] has studied the Lotka-Volterra predatorprey model with Holling type II functional response. Thismodel assumes that the number of assemblies perpredator is proportional to the obtainable additional food.Sen, et. al [5] discussed a two-species model in thepresence of forage and harvesting in predators using theHolling type II functional response. Then, Prasad [6]reviewed a model that took into account the parametersof handling time and nutritional value of food additives.Models combining disease in pests with pathogens(bacteria, fungi, and viruses) to infect pests andharvesting have also been introduced [7-8]. The pestpredator model [9] concatenating the effects of Alle onpests and food additives on predators. Sahoo [10]discusses food additives playing an important role insurvival in a biological conservation model. Manyresearchers have studied the modified Leslie-Gowermodel with different response functions [11-15]. Theproposed pest-predator model [16] incorporate anepidemic model and the Leslie-Gower likewise of pestCopyright 2021 The Authors. Published by Atlantis Press International B.V.This is an open access article distributed under the CC BY-NC 4.0 license 9

Advances in Engineering Research, volume 209harvesting. Mondal [17] developed a two-species modelwith the effect of fear and competition among prey. Themodel involves seasonal parameters in determining thequality and quantity of food additives. Inspired by themodel [18] which discussed the Leslie-Gower model andmodified by assumpting the additional food to predatorin terms of the handling time. In this article, we havestudied a prey-predator system with additional food forpredator and considered the effect of fear only on thebirth rate of the prey population. We also involvedadditional food to support predator growth in terms of thehandling time of Holling type II.known as the Leslie-Gower modification which isThe rest of the paper is sequenced as follows. Weconstruct the pest-predator model to consider the effectof fear for pest and addition food for predator in Section2. In Section 3, the existence and local stability of theequilibrium point are discussed. Numerical simulationsare performed in Section 4 by phase portrait andbifurcation diagram. The last section, we end withconcluding in Section 6.Based on the assumptions described above, theinteraction model between pest and predator is obtainedas follows2. MATHEMATICS MODELLINGwith π‘₯(𝑑) represents the population density of pests and𝑦(𝑑) represents the population density of predator at time𝑑. The parameters 𝑓, π‘˜, and 𝛽 represent the natural of fearof pest, carrying capacity of 𝑦, and maximum growth rateof 𝑦. The parameter 𝑛 and 𝐴 are the parameters whichcharacterize the additional food. All the parametersrelevant with the system (3) are positive.Based on the model [17] and [18], a prey growthmodel was constructed by involving the effect of fearwithout competition between preys and the additionalfood to predators. The main objective of this paper is toinvestigate parameters of the maximum value of growthrate of predators with additional food in controlling thebalance between populations. The dynamic analysiscarried out includes determining the equilibrium pointand the type of equilibrium for each solution of thesystem. In order to construct a mathematical model, thefollowing assumptions have been made in the presentstudy. Specifically, the model to be constructed isdescribed in the following subsection.2.1 Assumptions of the ModelThe pest population grows logistically with anintrinsic growth rate of r and it is assumed that the pestπ‘Ÿπ‘₯has a fear of predators so that the growth becomes.1 𝑓𝑦The growth rate of pests is reduced by the presence ofpredation or predation of predators on pests. Thepredation process is known as the functional responses.The parameter Ξ± is the maximum value of the growth rateof the predator. The growth rate of pests can be writtenas follows𝑑π‘₯π‘‘π‘‘π‘Ÿπ‘₯𝛼π‘₯𝑦 1 𝑓𝑦 π‘š π‘₯ 𝑛𝐴(1)The growth rate of predators does not only depend onthe prey population but also depends on theenvironmental carrying capacity to maintain the survivalof the predators. The predator growth rate model isexpressed as (1 𝑦π‘₯ π‘˜). This model considers thepresence of additional food for predators to survive ifthere is no main food. The parameters 𝛽 represents theefficiency with which the food consumed by the predatorgets converted into predator then the maximum growthrate of the predator.π‘‘π‘¦π‘‘π‘‘π‘¦πœŒπ‘›π΄π‘¦ 𝛽𝑦 (1 π‘₯ π‘˜) π‘š π‘₯ 𝑛𝐴(2)2.2 Mathematical Formulation of the Model𝑑π‘₯π‘Ÿπ‘₯𝛼π‘₯𝑦𝑑𝑑 1 𝑓𝑦 π‘š π‘₯ 𝑛𝐴𝑑𝑦𝑑𝑑 𝛽𝑦 (1 π‘₯ π‘˜) π‘š π‘₯ π‘›π΄π‘¦πœŒπ‘›π΄π‘¦(3)2.3 Equilibrium PointslThe dynamic analysis includes the determination ofthe equilibrium point, the existence of the equilibriumpoints and local stability analysis. Local stability analysisto determine the type of stability of each equilibriumpoint. Then the possible positive equilibrium point of thesystem (3) is obtained. The equilibrium point representsthe population density at equilibrium. Therefore, anequilibrium point is said to exist if every element is nonnegative.2.3.1 𝐸1 (0,0), where all populations are extinct.π‘˜(𝑛𝐴𝛽 π‘›π΄πœŒ π›½π‘š)2.3.2 𝐸2 (0,) , where only predator𝛽(𝑛𝐴 π‘š)survives. Represents the extinction of pestpopulations2.3.3 𝐸3 (π‘₯ , 𝑦 ), where pest and predator coexist.The population pest and predator are able tosurvive.And π‘₯ is a root of a fourth-degree equation withcomplicated coefficients. We provide sufficientconditions for the existence of a nonnegative root. for π‘₯ we get equation.𝐻1 (𝑦 )4 𝐻2 (𝑦 )3 𝐻3 (𝑦 )2 𝐻4 (𝑦 ) 𝐻5 0,(4)with 𝐻1 π‘Žπ›Όπ‘“, and π‘Ž 𝛼𝛽𝑓520

Advances in Engineering Research, volume 209𝐻2 π‘Ž(2𝛼 π‘Ÿ)𝐻3 π‘Žπ‘˜π‘Ÿ π‘Žπ‘šπ‘Ÿ π‘›π΄π‘Ÿ π‘›π΄π›Όπ‘“π‘ŸπœŒ 𝛼 2 𝛽 π›Όπ›½π‘Ÿπ»4 π‘›π΄π›Όπ‘ŸπœŒ π›Όπ›½π‘˜π‘Ÿ π‘›π΄π›Όπ›½π‘Ÿ π›Όπ›½π‘šπ‘Ÿπ»5 𝑛2 𝐴2 π‘Ÿ 2 𝜌 π‘›π΄π‘˜πœŒπ‘Ÿ 2 π‘›π΄π‘šπœŒπ‘Ÿ 2A fourth-degree equation has four roots in the complexdomain (4). Omitting to write explicitly its coefficients,in view of their complexity (4). Now we find sufficientconditions for it to have at least one positive root [19].Depending on the parameters of the system (3), there istwo equilibrium point 𝐸3 (π‘₯3 , 𝑦3 ) and 𝐸4 (π‘₯4 , 𝑦4 ).Theorema3. LOCAL STABILITY ANALYSISKolmogorov conditions [20] at (0,The stability properties of the equilibrium point ofsystem (3) is determined by the roots of the characteristicequation. Here, the Jacobian matrix at an equilibriumpoint is𝐽 [π‘Ÿπ›Όπ‘¦π›Όπ‘₯π‘¦π‘Ÿπ‘“π‘₯ 21 𝑓𝑦 𝑛𝐴 π‘š π‘₯ (𝑛𝐴 π‘š π‘₯) 1 𝑓𝑦𝛼π‘₯𝛽𝑦 2 𝑛𝐴 π‘š π‘₯ (π‘˜ π‘₯)2πœŒπ‘›π΄π‘¦π‘¦ 𝛽 (1 )(𝑛𝐴 π‘š π‘₯)2π‘˜ π‘₯π›½π‘¦πœŒπ‘›π΄ ]π‘˜ π‘₯ 𝑛𝐴 π‘š π‘₯The direct evaluation of the Jacobian matrix at 𝐸1 gives𝐽(𝐸1 ) [π‘Ÿ 0 0 𝛽 πœŒπ‘›π΄π‘›π΄ π‘š2.The(0,equilibriumπ‘˜(𝑛𝐴𝛽 π‘›π΄πœŒ π›½π‘š)𝛽(𝑛𝐴 π‘š))pointis𝐸2 locallyasymptotically stableProof.The equilibrium point 𝐸2 is locally asymptotically stableif 𝑇 0 and 𝐷 0.The trace (𝑇) and the determinant (𝐷) of the Jacobianmatrix at 𝐸2 are determined by πœ†2 π‘‡πœ† 𝐷 0, where𝑇 π‘Ž1 π‘Ž3 and 𝐷 π‘Ž1 π‘Ž3 . The system (3) satisfies theπ‘˜(𝑛𝐴𝛽 π‘›π΄πœŒ π›½π‘š)𝛽(𝑛𝐴 π‘š))making 𝐷 π‘Ž1 π‘Ž3 positive. Therefore 𝐸2 is locallyasymptotically stable if 𝑇 0 and unstable if 𝑇 0. Wehave𝑇 π‘Ÿπ‘“π‘˜(𝛽𝑛𝐴 πœŒπ‘›π΄ π›½π‘š) 1𝛽(𝑛𝐴 π‘š)π›Όπ‘˜(𝛽𝑛𝐴 πœŒπ‘›π΄ π›½π‘š) 𝛽(𝑛𝐴 π‘š)2𝛽𝑛𝐴 πœŒπ‘›π΄ π›½π‘š 𝛽 (1 )𝛽(𝑛𝐴 π‘š)𝛽𝑛𝐴 πœŒπ‘›π΄ π›½π‘šπœŒπ‘›π΄ 𝑛𝐴 π‘šπ‘›π΄ π‘šHere it is important that the term 𝑇 0 and 𝐷 is alwayspositive and this completes the proof.Similarly, the Jacobian matrix at 𝐸3 is],Theorema 1. The equilibrium point 𝐸1 (0,0) isalways unstable.𝐽(𝐸3 ) [π‘Ž4 π‘Ž5 π‘Ž6 π‘Ž7 ]Theorem 3. The equilibrium point 𝐸3 (π‘₯ , 𝑦 ) islocally asymptotically stableProof.The characteristic equation of the matrix J( 𝐸1 ) are(πœ† π‘Ÿ)(π‘›π΄πœ† π‘šπœ† 𝐴𝑛𝛽 π‘›π΄πœŒ π‘šπ›½) 0 . It isObvious that one of eigenvalue πœ†1 π‘Ÿ is positive, theother eigenvalues is always positive πœ†2 𝐴𝑛𝛽 π‘›π΄πœŒ π‘šπ›½π‘›π΄ π‘š 0. Hence, 𝐸1 is an unstable.Proof.Clearly that two eigenvalues are determined by πœ†2 π‘‡πœ† 𝐷 0, where 𝑇 π‘Ž4 π‘Ž6 and 𝐷 π‘Ž4 π‘Ž7 π‘Ž5 π‘Ž6 .Therefore 𝐸3 is stable if 𝑇 0 and 𝐷 0. The proof iscomplete.The evaluation of the Jacobian matrix at 𝐸2 gives4. NUMERICAL SIMULATIONS𝐽(𝐸2 ) [π‘Ž1 0 π‘Ž2 π‘Ž3 ], withWe would like to convey a numerical simulation toillustrate bifurcation phenomena. The study numeric arevery important to solving of solution the system (3)which is undertaken by Python 3.7. Numericalsimulations are carried out to support the analysis anddisplay the change in the equilibrium point solutionthrough a bifurcation diagram.π‘Ÿπ‘Ž1 π‘“π‘˜(𝛽𝑛𝐴 πœŒπ‘›π΄ π›½π‘š)𝛽(𝑛𝐴 π‘š)π‘Ž2 1 π›Όπ‘˜(𝛽𝑛𝐴 πœŒπ‘›π΄ π›½π‘š)𝛽(𝑛𝐴 π‘š)2(𝛽𝑛𝐴 πœŒπ‘›π΄ π›½π‘š) π‘›π΄πœŒπ‘˜(𝛽𝑛𝐴 πœŒπ‘›π΄ π›½π‘š) 𝛽(𝑛𝐴 π‘š)2𝛽(𝑛𝐴 π‘š)3π‘Ž3 𝛽 (1 𝛽𝑛𝐴 πœŒπ‘›π΄ π›½π‘šπ›½π‘›π΄ πœŒπ‘›π΄ π›½π‘š) 𝛽(𝑛𝐴 π‘š)𝑛𝐴 π‘šπœŒπ‘›π΄ 𝑛𝐴 π‘š521

Advances in Engineering Research, volume 209Table 1. The set of parameter value used for tionMaximum growth rateof pestThe fear effect of pestto predatorMaximum rate ofpredatorHalf saturation valueof the predatorThe relative ability ofthe predator to detectadditional foodAmount of additionalfood to the g capacity ofpredator2.1𝛽Maximum growth rateof the l condition 𝑁 [π‘₯(0) 5, 𝑦(0) 7.2]. Thisoccurs quickly since the initial value is taken chose to 𝑁.The limit cycle encourages an almost periodic solutionwhen 𝛼 increases. The equilibrium 𝐸1 (0,0) unstableremains itself. The interior equilibrium 𝐸3 (5.763726, 8.479635) evolves into the positive periodicsolution. We find the Hopf bifurcation when 𝛼 1 0.72993019 and a stable limit cycle appears around theinteriorequilibriumpointfor𝐸3 (5.763726, 8.479635) in Figure 1b. Now, we discussfour different parameters value (𝛼) to illustrate thesolution tends to the equilibrium point. The dynamics ofthe two populations of the present system (3) are obviousat the eight frames shown in the Figure 2a to 5b.4.1 Phase PortraitFor simulation, we take the same parameter values inTable 1. Using these parameter values, it can be shownthat all equilibrium points 𝐸1 , 𝐸2 , 𝐸3 , and 𝐸4 of thesystem (3) exist. However, we perform the numericalsimulation showing that system (3) the limit cycleundergoes periodic perturbation.Figure 2a The phase portraits of system (3) which shows𝐸3 stable.Figure 2b The solution tends to 𝐸3 stable at 𝛼 0.658321.Figure 1a The phase portraits of system (3) which showsHopf Bifurcation at 𝛼 0.72993019.Figure 3a The phase portraits of system (3) whichshows 𝐸3 stable.Figure 1b Hopf Bifurcation Diagram with specify of thelimit cycle at 𝛼 0.72993019.In Figure 1a, we illustrate that the system (3) gets alimit cycle when parameter value 𝛼 0.72993019 with522

Advances in Engineering Research, volume 209Figure 3b The dynamics tends to 𝐸3 stable at 𝛼 0.7.Figure 4a The phase portraits of system (3) whichshows 𝐸3 stable.Figure 5b The solution tends to 𝐸2 (0, 3.047)at 𝛼 0.866893.The phase portraits of the system (3) which the solutiontends to 𝐸3 (5.5284, 8.24679) stable when parameter𝛼 0.658321 shown in Figure 2a and 2b. Figure 3a and3b shows that all the equilibrium points 𝐸1 , 𝐸2 , 𝐸3 , and 𝐸4exists. This simulation uses the parameters as shown inTable 1, that the stability conditions at the equilibriumpoint 𝐸3 (6.4863, 9.1956) fulfill the results of thestability conditions. The red line corresponds to the pest(π‘₯) population and the black line correspond to thepredator (𝑦) population in Figure (2b – 5b). Numerically,the system (3) indicates a kind dynamic fullness.4.2 Bifurcations around the interior equilibriumpointNumerical continuity is performed on an equilibriumsolution with a variation of one parameter to indicate anindication of a change in the type of stability usesMatCont. Changes in stability indicate the emergence ofbifurcations, namely Hopf bifurcation, Saddle Nodebifurcation, and Transcritical bifurcation.Figure 4b The dynamics of the system (3) at 𝛼 0.73994233.Figure 5a The phase plane diagram of the system (3)stable.Figure 6 Bifurcation Diagram of the predator population(𝑦) with continuation parameter 𝛼.In numerical continuity, the parameter (𝛼) is to indicatechanges in the stability of several the equilibrium point.Figure 6 presents the bifurcation diagram of the solutionof the system (3) which is varying the parameter of themaximum rate of the predator predation to the pestpopulation (𝛼).523

Advances in Engineering Research, volume 209a. Saddle node BifurcationIn detail the changes that occur at the interiorequilibrium point are shown in Figure 6 diagram ofbifurcation for the predator population (π’š) with respect toparameter 𝜢. The results of the numerical continuation ofthe parameter 𝛼 show the changes that occur in thestability at the interior equilibrium point ( π‘¬πŸ‘ ). TheBifurcation diagram in Figure 6 shows for𝟎. πŸ•πŸπŸ—πŸ—πŸ‘πŸŽπŸπŸ— 𝜢 𝟎. πŸ–πŸ”πŸ”πŸ–πŸ—πŸ’. There are two interiorequilibrium point where of them is (π‘¬πŸ‘ ) unstable while(π‘¬πŸ’ ) is stable. Both conditions of the interior equilibriumpoint crash at 𝜢 𝟎. πŸ–πŸ”πŸ”πŸ–πŸ—πŸ’, namely Limit Point (LP).The phenomenon of the emergence of LP shows thatthere is a Saddle-node (Fold) bifurcation which is drivenby the parameter of the maximum value of the predatorpredation rate on the pest. if 𝜢 𝟎. πŸ–πŸ”πŸ”πŸ–πŸ—πŸ‘πŸ“ , ( π‘¬πŸ )stable.b. Double stability phenomenonAnother interesting dynamics behavior to observe asshown in Figure 6 is the appearance of two differentstability, known as the bi-stability phenomenon. Thisphenomenon occurs during 0.866893 𝛼 0.866894that the system (3) has a double stability. There are twostability in the solution of system (3) namely the interiorequilibrium point (𝐸4 ) and the pest extinction equilibriumpoint (𝐸2 ) which are locally asymptotically stable, whilethe other interior equilibrium point are unstable. Thephenomenonalsooccurs0.658321 𝛼 0.72993019. The solution of the interior equilibriumpoint (𝐸3 ) and the pest extinction equilibrium point (𝐸2 )which are locally asymptotically stable.c. Transcritical BifurcationThe bifurcation diagram in Figure 6 illustrates theexchange between the equilibrium interior point (𝐸3 ) andthe pest population extinction points ( 𝐸2 ). Thisphenomenon shows a Transcritical bifurcation. For𝛼 0.658321, the pest population extinction points (𝐸2 )are unstable. As it increases of the parameter 𝛼, a BranchPoint (BP) apprears at 𝛼 0.658321. This BP indicatesa Transcritical bifurcation, while a change in theequilibrium point of the pest population extinction points(𝐸2 ), which was initially unstable for 𝛼 0.658321,became stable for 𝛼 0.658321. On the other hand, thereis a change in the coexist equilibrium point 𝐸3 , which wasoriginally stable 𝛼 0.658321 , became unstable for𝛼 0.658321.four equilibrium points. There is one equilibriumcondition that is always unstable, namely the equilibriumpoint of extinction for all populations. The otherequilibrium points are stable with certain conditions thathave been proven. The results of the dynamic analysishave been confirmed through numerical simulations bycontinuing the parameter of the maximum rate of thepredator predation, namely 𝛼. The numerical simulationresults also show that the pest-predator interaction modeldescribes rich dynamics with the occurrence of Hopfbifurcation, Transcritical bifurcations, Saddle-nodebifurcations and double stability phenomena driven bythe continuation of the maximum value parameter ofMaximum rate of predator predation on pests.AUTHORS’ CONTRIBUTIONSDS: Conceptualization, Data curation, Visualization,software (simulation and continuation numeric) anddrafting manuscript: M and A; Formal analysis, Fundingacquisition, and review. M.J; Methodology, datavisualization and editing. All authors have read andapproved the final manuscript.REFERENCES[1]N.A. Herawati and Sudarmaji, Helminths of theRice-field Rat, Rattus argentiventer, In G.RSingleton (Ed.), Rat, Mice and People: RodentBiology and Management, ACIAR Canberra,2003.[2]R. Kaliky, K. Yolanda, and Sudarmaji, PeranKeanekaragaman Hayati untuk MendukungIndonesia sebagai Lumbung Pangan Dunia,Seminar Nasional dalam Rangka Dies NatalisUNS ke 42 Tahun 2018, 2(1)( 2018) c.id/6858/1/Makalah%20Seminar%20UNS Tempe Samsul%20Rizal%20UNILA REVISI.pdf[3]N.T. Haryadi, M. W. Jadmiko and T. Agustina.,Pemanfaatan Burung Hantu untuk MengendalikanTikus di Kecamatan Semboro Kabupaten ac.id/handle/123456789/73295[4]P. D. N. Srinivasu, B. S. R. V. Prasad and M.Venkatesulu, Biological Control ThroughProvision of Additional Food to Predators,Theoretical Population Biology, University ofMissouri, Kansas City, USA,2007, pp 111-120.DOI: http://dx.doi.org/10.1016/j.tpb.2007.03.011[5]Sen, et. al, Global Dynamics of an Additional FoodProvided Predator-Prey System with ConstantHarvest in Predators, Applied Mathematics andComputation 250 (2015) 193-211. DOI:http://dx.doi.org/10.1016/j.amc.2014.10.0855. CONCLUSIONWe have discussed a model describing pest-predatorinteractions taking into account the effects of fear on pestpopulations and food additives on predator populations.The predator growth model uses a modified LeslieGower model. We find that the pest-predator model has524

Advances in Engineering Research, volume 209[6][7][8]B. S. R. V. Prasad, M. Banerjee and P. D. N.Srinivasu, Dynamics of Additional Food ProvidedPredator-Prey System with Mutually InterferingPredators, Mathematical Biosciences j.mbs.2013.08.013[17]A. Suryanto, I. Darti and S. Anam, Stabilityanalysis of pest-predator interaction model withinfectious disease in prey, AIP ConferenceProceedings 1937(1) (2017) p 020018. DOI:http://dx.doi.org/10.1063/1.5026090S. Mondal, A. Maiti and G.P. Samanta, Effects ofFear and Additional Food in a Delayed PredatorPrey Model, Biophysical Reviews and Letter 3048018500091.[18]H.M. Ulfa, A. Suryanto and I. Darti, Dynamics ofLeslie-GowerPredator-preyModelwithadditional food for Predator, International Journalof Pure and Applied Mathematics 115(2) (2017)199-209.DOI: 10.12732/ijpam.v115i2.1[19]N. Ali, M. Haque, E. Venturino and S Chakravart,Dynamics of a three species ratio-dependent foodchain model with intra-specific competiton withinthe top predator, Computers in Biology .compbiomed.2017.04.007[20]K. Sigmund, Kolmogorov and populationdynamics. In Charpentier, E., Lesne, A., Nikolski,N.K., (Eds.), Kolmogorov’s Heritage inMathematics, Springer-Verlag, Berlin, 2007, pp.177-187. DOI: https://doi.org/10.1007/978-3-54036351-4 9S.K. Sasmal, D.S. Mandal and J. Chattopadhyay,A Predator-pest Model with Allee Effect and PestCulling and Addition Food Provision to thePredator-Application to Pest Control, Journal ofBiological System 25(2) (2017) 295-326. DOI:https://doi.org/10.1142/S0218339017500152[9]Z. Zhu, R. Wu, L. Lai and X. Yu, The Influence offear effect to the Lotka-Volterra predator-preySystem with Predator has other food Resource,Advances in Difference Equations 1 (2020) ]B. Sahoo, Predator-prey System with SeasonallyVarying Additional Food to Predators,International Journal of Basic and .org/10.14419/ijbas.v1i4.205[11]M. Aziz-Alaoui, M.D. Okiye, Boundedness andglobal stability for a predator-prey model withmodified Leslie-Gower and Holling-type IIschemes, Applied Mathematics Letters 16 010/813289[12]S. Yu, Global asymptotic stability a onal response, Advances in rg/10.1186/1687-1847-2014-84[13]R.P. Gupta, P. Chandra, Bifurcation analysis ofmodified Leslie-Gower predator prey model withMichaelis-Menten type prey harvesting, Journal ofMathematical Analysis and Applications 6/j.jmaa.2012.08.057[14]I. Darti, A. Suryanto, Dynamics preservingnonstandard Finite difference method for themodified Leslie-Gower predator-prey model withHolling type II functional responses. Far EastJournal of Mathematical Sciences 99(5) 99050719[15]D.Savitri, A. Suryanto, W.M. Kusumawinahyuand Abadi, Dynamical Behavior of a ModifiedLeslie–Gower One Prey–Two Predators withCompetition, Mathematics 8(5) (2020) 669. DOI:http://dx.doi.org/10.3390/math8050669[16]A. Suryanto and I. Darti, Dynamics of LeslieGower Pest-Predator Model with Disease in on of Pesticide., International Journalof Mathematics and Mathematical Sciences (2019)1-9. DOI: https://doi.org/10.1155/2019/5079171.525

model involves seasonal parameters in determining the quality and quantity of food additives. Inspired by the model [18] which discussed the Leslie-Gower model and modified by assumpting the additional food to predator in terms of the handling time. In this article, we have studied a prey-predator system with additional food for

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