=Paper=
{{Paper
|id=Vol-2748/Paper59
|storemode=property
|title=Numerical Solutions of the Variable-Order Space Fractional Activator-Inhibitor Reaction-Diffusion Systems
|pdfUrl=https://ceur-ws.org/Vol-2748/IAM2020_paper_59.pdf
|volume=Vol-2748
|authors=Redouane Douaifia,Salem Abdelmalek
|dblpUrl=https://dblp.org/rec/conf/iam/Douaifia020
}}
==Numerical Solutions of the Variable-Order Space Fractional Activator-Inhibitor Reaction-Diffusion Systems==
Numerical solutions of the variable-order space fractional activator-inhibitor reaction-diffusion systems Redouane Douaifiaa , Salem Abdelmaleka,b a Laboratory of Mathematics, Informatics and Systems (LAMIS), Larbi Tebessi University – Tebessa, Algeria b Department of Mathematics and Computer Science, Larbi Tebessi University – Tebessa, Algeria Abstract Reaction–diffusion equations containing fractional derivatives can provide adequate mathematical mod- els for explaining anomalous diffusion and transport dynamics in complex systems that can not be ad- equately modeled by standard numerical order equations. Researchers have recently found that many physical processes display fractional order dynamics that differs with time or space. The continuity of order in the fractional calculation allows the order of the fractional operator to be regarded as a variable. The Samko–Ross variable-order fractional operator can be viewed as a generalization of the Riemann– Liouvile type definition. Although this definition is the most appropriate definition having fundamen- tal characteristics that are desirable for physical modeling, numerical methods for reaction–diffusion activator–inhibitor systems using this definition have not yet appeared in the literature. In this paper, we provide a numerical method to get the approximate solutions of the variable-order space-fractional Activator–inhibitor systems, namely the reaction–diffusion system with cubic nonlinearity and Brus- selator model on a 1–D space–domain, we adopt the Riesz variable–order space fractional derivative. Numerical simulations demonstrate that the finite difference approach is computationally efficient. Keywords Variable–order calculus, activator–inhibitor systems, numerical simulation 1. Introduction In recent decades, fractional derivatives have been commonly used in the modeling of complex physical and mechanical phenomena in wide classes of complex media with hereditary, fractal and non-markovian properties, is a field of rapidly growing interest with applications in many different fields. These include the study of biology [1], hydrology [2], biochemistry [3], finance [4], and physics [5]. But researchers have found that many important dynamic processes show fractional order behavior that may change with time and / or space. This fact suggests that differential calculus is a natural candidate to provide an effective mathematical framework to describe the complex dynamic problems that appear in different biological and chemical mod- els, such as viscoelastic materials, anomalous diffusion. In reaction diffusion systems which can be described by two variables, one has the notion of an activator and an inhibitor. In that case, be the diffusion coefficient of the inhibitor greater than the diffusion coefficient of the IAM’20: Third conference on informatics and applied mathematics, 21–22 October 2020, Guelma, ALGERIA " redouane.douaifia@univ–tebessa.dz (R. Douaifia); salem.abdelmalek@univ–tebessa.dz (S. Abdelmalek) 0000-0001-6960-4572 (R. Douaifia); 0000-0001-9762-9654 (S. Abdelmalek) © 2020 Copyright for this paper by its authors. Use permitted under Creative Commons License Attribution 4.0 International (CC BY 4.0). CEUR Workshop Proceedings http://ceur-ws.org ISSN 1613-0073 CEUR Workshop Proceedings (CEUR-WS.org) activator if spontaneous steady-state patterns are to occur. Thus, pattern formation is said to occur as a result of "short range activation" and "long range inhibition", the activator-inhibitor reaction-diffusion systems model was used to simulate pattern forming processes. In this work we show the behavior of solutions for activator-inhibitor models with variable superdiffusion by remplacing the second derivative in space by the variable order Riesz fractional deriva- tive. The studies of dynamics and numerical simulations of fractional-space activator–inhibitor reaction–diffusion systems have recently met with the interest of researchers (cf. [6, 7]). 2. Variable–order fractional derivative In [8, 9] Samko and Ross directly generalized the Riemann-Liouvile and Marchaud fractional integration and differentiation of the case of variable order and discussed some properties and the inversion formula . It has become a controversial research and has raised widespread con- cern in the last years. This section is devoted to the most important definitions of variable–order direvatives. 2.1. Variable–order Riemann–Liouville fractional derivatives Left derivative: 𝜉 𝛼(𝑡,𝑥) 1 𝜕𝑚 𝑎 𝐷𝑥 𝑢(𝑡, 𝑥) = (𝜉 − 𝜆)𝑚−𝛼(𝑡,𝑥)−1 𝑢(𝑡, 𝜆)𝑑𝜆 [ Γ(𝑚 − 𝛼(𝑡, 𝑥)) 𝜕𝜉 𝑚 ∫𝑎 ]𝜉 =𝑥 Right derivative: 𝑏 𝛼(𝑡,𝑥) (−1)𝑚 𝜕𝑚 𝑥 𝐷𝑏 𝑢(𝑡, 𝑥) = (𝜆 − 𝜉 )𝑚−𝛼(𝑡,𝑥)−1 𝑢(𝑡, 𝜆)𝑑𝜆 [ Γ(𝑚 − 𝛼(𝑡, 𝑥)) 𝜕𝜉 𝑚 ∫𝜉 ] 𝜉 =𝑥 where Γ(.) is gamma function and 𝑚 − 1 < 𝛼(𝑡, 𝑥) ⩽ 𝑚, 𝑚 ∈ ℕ. 2.2. Variable-order Grünwald-Letnikov fractional derivatives Left derivative: 𝑛 𝐺 𝛼(𝑡,𝑥) 𝛼(𝑡, 𝑥) 𝑎 𝐷𝑥 𝑢(𝑡, 𝑥) = lim ℎ−𝛼(𝑡,𝑥) ∑(−1)𝑗 𝑢(𝑡, 𝑥 − 𝑗ℎ) ℎ→0,𝑛ℎ=𝑥−𝑎 𝑗=0 ( 𝑗 ) Right derivative: 𝑛 𝐺 𝛼(𝑡,𝑥) 𝛼(𝑡, 𝑥) 𝑥 𝐷𝑏 𝑢(𝑡, 𝑥) = lim ℎ−𝛼(𝑡,𝑥) ∑(−1)𝑗 𝑢(𝑡, 𝑥 + 𝑗ℎ) ℎ→0,𝑛ℎ=𝑏−𝑥 𝑗=0 ( 𝑗 ) where 𝛼(𝑡, 𝑥) Γ(𝛼(𝑡, 𝑥) + 1) = , ( 𝑗 ) Γ(𝑗 + 1)Γ(𝛼(𝑡, 𝑥) − 𝑗 + 1) and 𝑚 − 1 < 𝛼(𝑡, 𝑥) ⩽ 𝑚, 𝑚 ∈ ℕ. 2.3. Variable–order Riesz fractional derivative 𝜕 𝛼(𝑡,𝑥) 𝑢(𝑡, 𝑥) 1 𝛼(𝑡,𝑥) =− [ 𝛼(𝑡,𝑥) 𝑎 𝐷𝑥 𝑢(𝑡, 𝑥) +𝑥 𝐷𝑏𝛼(𝑡,𝑥) 𝑢(𝑡, 𝑥)] . 𝜕 |𝑥| 2 cos ( 𝜋𝛼(𝑡,𝑥) 2 ) 3. General Activator-inhibitor model Consider a 2-species reaction-diffusion system 𝜕𝑢 𝜕𝑣 = 𝐷𝑢 Δ𝑢 + 𝐹 (𝑢, 𝑣), = 𝐷𝑣 Δ𝑣 + 𝐺(𝑢, 𝑣) 𝜕𝑡 𝜕𝑡 Assume there exists a constant steady state 𝐸𝑒𝑞 = (𝑢𝑒𝑞 , 𝑣𝑒𝑞 ), 𝐹 (𝑢𝑒𝑞 , 𝑣𝑒𝑞 ) = 𝐺(𝑢𝑒𝑞 , 𝑣𝑒𝑞 ) = 0 The Jacobian of the previous system is defined by 𝜕𝐹 𝜕𝐹 ⎛ 𝜕𝑢 |𝐸𝑒𝑞 𝜕𝑣 |𝐸𝑒𝑞 ⎞ 𝐽 𝐽 𝐽 |𝐸𝑒𝑞 = 11 12 = ⎜ ⎟ (𝐽21 𝐽22 ) ⎜ 𝜕𝐺 𝜕𝐺 ⎟ ⎝ 𝜕𝑢 |𝐸𝑒𝑞 𝜕𝑣 |𝐸𝑒𝑞 ⎠ We say that the reaction diffusion system is the inhibitory activator system if the coefficients of its Jacobian matrix have the following relationships: 𝐽11 𝐽22 < 0, 𝐽12 𝐽21 < 0 The species that achieve 𝐽𝑖𝑖 > 0, (𝐽𝑖𝑖 < 0) is called activator (inhibitor), respectively (𝑖 = 1, 2). 4. The variable order space fractional Activator-inhibitor models 4.1. Variable order space fractional reaction–diffusion model with cubic nonlinearity We consider the reaction-diffusion model with cubic nonlinearity in one-dimensional space, by replacing the classical spatial differential operators by variable order Riesz fractional analogues , we obtain the following system 𝜕𝑢 𝜕 𝛼(𝑡,𝑥) 𝑢 1 = 𝐷𝑢 𝛼(𝑡,𝑥) + 𝑢 − 𝑢 3 − 𝑣, in [0, 𝑇 ] × [𝑎, 𝑏] , (1) 𝜕𝑡 𝜕 |𝑥| 3 𝜕𝑣 𝜕 𝛼(𝑡,𝑥) 𝑣 = 𝐷𝑣 + 𝑢 − 𝑣 + 𝐴, in [0, 𝑇 ] × [𝑎, 𝑏] , (2) 𝜕𝑡 𝜕 |𝑥|𝛼(𝑡,𝑥) and the initial and boundary conditions 𝑢(0, 𝑥) = 𝑢0 (𝑥), 𝑣(0, 𝑥) = 𝑣0 (𝑥), on [𝑎, 𝑏] , (3) 𝑢(𝑡, 𝑎) = 𝑢(𝑡, 𝑏) = 𝐵𝐶𝑢 , 𝑣(𝑡, 𝑎) = 𝑣(𝑡, 𝑏) = 𝐵𝐶𝑣 , ∀𝑡 ∈ [0, 𝑇 ] . (4) Here 𝑢, 𝑣 represent the concentrations of two species having the diffusion rates 𝐷𝑢 , 𝐷𝑣 > 0, 𝐴 ∈ ℝ, 𝐵𝐶𝑢 ⩾ 0 and 𝐵𝐶𝑣 ⩾ 0 are external parameters. 4.2. Variable order space fractional Brusselator model We consider the well-known reaction-diffusion model Brusselator in one-dimensional space, by replacing the classical spatial differential operators by variable order Riesz fractional analogues , we get the following system 𝜕𝑢 𝜕 𝛼(𝑡,𝑥) 𝑢 = 𝐷𝑢 + 𝐴 − (𝐵 + 1)𝑢 + 𝑣𝑢 2 , in [0, 𝑇 ] × [𝑎, 𝑏] , (5) 𝜕𝑡 𝜕 |𝑥|𝛼(𝑡,𝑥) 𝜕𝑣 𝜕 𝛼(𝑡,𝑥) 𝑣 = 𝐷𝑣 + 𝐵𝑢 − 𝑣𝑢 2 , in [0, 𝑇 ] × [𝑎, 𝑏] , (6) 𝜕𝑡 𝜕 |𝑥|𝛼(𝑡,𝑥) and the initial and boundary conditions 𝑢(0, 𝑥) = 𝑢0 (𝑥), 𝑣(0, 𝑥) = 𝑣0 (𝑥), on [𝑎, 𝑏] , (7) 𝑢(𝑡, 𝑎) = 𝑢(𝑡, 𝑏) = 𝐵𝐶𝑢 , 𝑣(𝑡, 𝑎) = 𝑣(𝑡, 𝑏) = 𝐵𝐶𝑣 , ∀𝑡 ∈ [0, 𝑇 ] . (8) The species 𝑢, 𝑣 represent the concentrations of two intermediary reactants having the dif- fusion rates 𝐷𝑢 , 𝐷𝑣 > 0 and 𝐴, 𝐵 > 0 are fixed concentrations, and 𝐵𝐶𝑢 , 𝐵𝐶𝑣 are external parameters (nonnegative numbers). 5. Explicit Euler Approximation We show the approximate solutions for systems (1)-(4) and (5)-(8) by applying the explicit finite difference method which described in [10]. We consider the numerical approximation in the time domain [0, 𝑇 ] and the space domain [𝑎, 𝑏]. Let 𝑡𝑘 = 𝑘Δ𝑡 (0 ⩽ 𝑡𝑘 ⩽ 𝑇 ), 𝑘 = 0, … , 𝑀, 𝑥𝑖 = 𝑎 + 𝑖Δ𝑥 (𝑎 ⩽ 𝑥𝑖 ⩽ 𝑏), 𝑖 = 0, … , 𝑁 , where the time step is Δ𝑡 = 𝑀 𝑇 and the space step is sec(𝜋𝛼 𝑘 ) 𝑁 . We denote that 𝑢𝑖 = 𝑢(𝑡𝑘 , 𝑥𝑖 ), 𝛼𝑖 = 𝛼(𝑡𝑘 , 𝑥𝑖 ), 𝑐𝑖 = − Δ𝑥 = 𝑏−𝑎 . The approximate Grün- 𝑘 𝑘 𝑘 𝑖 2 wald formulas for the variable-order Riemann-Liouville fractional derivatives approximation show as follow: 𝑖+1 𝛼𝑘𝑖 𝐺 𝑖𝛼𝑘 −𝛼𝑖+1 𝑘 (𝑗) 𝑘 𝑎 𝐷𝑥𝑖 𝑢(𝑡𝑘 , 𝑥𝑖 ) =𝑎 𝐷𝑥𝑖 𝑢(𝑡𝑘 , 𝑥𝑖 ) ≈ (Δ𝑥) ∑ 𝑔𝛼 𝑘 𝑢𝑖+1−𝑗 𝑖+1 𝑗=0 𝑁 −𝑖+1 𝛼𝑖𝑘 𝐺 𝛼𝑖𝑘 𝑘 −𝛼𝑖−1 𝑘(𝑗) 𝑥𝑖 𝐷𝑏 𝑢(𝑡𝑘 , 𝑥𝑖 ) =𝑥𝑖 𝐷𝑏 𝑢(𝑡𝑘 , 𝑥𝑖 ) ≈ (Δ𝑥) ∑ 𝑔𝛼 𝑘 𝑢𝑖−1+𝑗 𝑖−1 𝑗=0 where 𝑔𝛼(𝑗)𝑘 is the Grünwald weights defined by 𝑖 𝛼𝑖𝑘 + 1 𝑔𝛼(0)𝑘 = 1, 𝑔𝛼(𝑗)𝑘 = 1− 𝑔 (𝑗−1) , (𝑗 = 1, 2, … ) 𝑖 𝑖 ( 𝑗 ) 𝛼𝑖𝑘 Therefore, the equations (1)-(2) and (5)-(6) can be discretized as follow: 𝑖+1 𝑁 −𝑖+1 𝑢𝑖𝑘+1 = 𝑢𝑖𝑘 + 𝐷𝑢 (1) 𝑟𝑖,𝑘 (𝑗) 𝑘 ∑ 𝑔𝑖+1,𝑘 𝑢𝑖+1−𝑗 (2) + 𝑟𝑖,𝑘 (𝑗) 𝑘 ∑ 𝑔𝑖−1,𝑘 𝑢𝑖−1+𝑗 + Δ𝑡𝐹 (𝑢𝑖𝑘 , 𝑣𝑖𝑘 ) (9) ( 𝑗=0 𝑗=0 ) 𝑖+1 𝑁 −𝑖+1 𝑣𝑖𝑘+1 = 𝑣𝑖𝑘 + 𝐷𝑣 𝑟 (1) ∑ 𝑔 (𝑗) 𝑣𝑖+1−𝑗 𝑘 (2) + 𝑟𝑖,𝑘 (𝑗) 𝑘 ∑ 𝑔𝑖−1,𝑘 𝑣𝑖−1+𝑗 + Δ𝑡𝐺(𝑢𝑖𝑘 , 𝑣𝑖𝑘 ) (10) ( 𝑖,𝑘 𝑗=0 𝑖+1,𝑘 𝑗=0 ) where 𝑟𝑖,𝑘 = Δ𝑡𝑐𝑖𝑘 (Δ𝑥)−𝛼𝑖+1 , 𝑟𝑖,𝑘 = Δ𝑡𝑐𝑖𝑘 (Δ𝑥)−𝛼𝑖−1 , 𝑔𝑖,𝑘 = 𝑔𝛼(𝑗)𝑘 and (1) 𝑘 (2) 𝑘 (𝑗) 𝑖 ⎧ ⎪ 𝐹 (𝑢 𝑘 , 𝑣 𝑘 ) = 𝑢𝑖𝑘 − 13 (𝑢𝑖𝑘 )3 − 𝑣𝑖𝑘 ⎧ ⎪ 𝐹 (𝑢 𝑘 , 𝑣 𝑘 ) = 𝐴 − (𝐵 + 1)𝑢𝑖𝑘 + 𝑣𝑖𝑘 (𝑢𝑖𝑘 )2 ⎪ 𝑖 𝑖 ⎪ 𝑖 𝑖 ⎨ 𝑜𝑟 ⎨ ⎪ 𝑘 𝑘 ⎪ ⎪ ⎩𝐺(𝑢𝑖 , 𝑣𝑖 ) = 𝑢𝑖𝑘 − 𝑣𝑖𝑘 + 𝐴 ⎪ 𝑘 𝑘 ⎩𝐺(𝑢𝑖 , 𝑣𝑖 ) = 𝐵𝑢𝑖𝑘 − 𝑣𝑖𝑘 (𝑢𝑖𝑘 )2 The stability and convergence of the explicit Euler approximation are descused in [10]. 6. Numerical experiments In this section, we show approximate solutions for the systems (1)-(4) and (5)-(8) to demon- strate the changes in solutions behaviour that arise when the exponent is varied from integer order to fractional order to variable order, and to identify the differences between solutions. The computer algorithm for numerical method (9)-(10), was written in Matlab, throughout the simulations we took the following values: 𝑎 = 0, 𝑏 = 4, 𝑇 = 20, spatial and time steps respec- 2 tively Δ𝑥 = 204 , Δ𝑡 = (Δ𝑥) 2 − 0.001. 6.1. Reaction-diffusion model with cubic nonlinearity We take, 𝐴 = −0.1, 𝐷𝑢 = 0.05, 𝐷𝑣 = 1, 𝐵𝐶𝑢 = 0.0503, 𝐵𝐶𝑣 = 0.07504 and the initial conditions: { 𝑢0 (𝑥) = 0.0503 − 10−3 cos(2𝜋𝑥) + 10−3 cos(5𝜋𝑥) 𝑣0 (𝑥) = 0.02504 + 10−3 cos(2𝜋𝑥) + 10−3 cos(5𝜋𝑥) The figure 1 shows the approximate solution for system (1)-(4) for 𝛼(𝑡, 𝑥) = 2, when the deriva- tive is fractional order 𝛼(𝑡, 𝑥) = 1.35 we can see the sulotions in figure 2. The behaviour of the solution is particularly interesting for the case 𝛼(𝑡, 𝑥) = 1.5 + 0.4 cos(𝑡𝑥) ∗ sin(2𝑡), see figure 3. Figure 1: Approximate solution of (1)-(4), for 𝛼(𝑡, 𝑥) = 2, where 𝑢1 = 𝑢 and 𝑢2 = 𝑣. Figure 2: Approximate solution of (1)-(4), for 𝛼(𝑡, 𝑥) = 1.35, where 𝑢1 = 𝑢 and 𝑢2 = 𝑣. 6.2. Brusselator model We take, 𝐴 = 1, 𝐵 = 3, 𝐷𝑢 = 0.05, 𝐷𝑣 = 1, 𝐵𝐶𝑢 = 1.09, 𝐵𝐶𝑣 = 2.02504 and the initial conditions: { 𝑢0 (𝑥) = 1.09 − 10−2 cos(2𝜋𝑥) + 10−3 cos(5𝜋𝑥) 𝑣0 (𝑥) = 2.02504 + 10−2 cos(2𝜋𝑥) + 10−3 cos(5𝜋𝑥) Figure 4 shows the behavior of the numerical solution for system (5)-(8) with 𝛼(𝑡, 𝑥) = 2, when the derivative is fractional order 𝛼(𝑡, 𝑥) = 1.35 we can see the sulotions in figure 5. The Figure 3: Approximate solution of (1)-(4), for 𝛼(𝑡, 𝑥) = 1.5 + 0.4 cos(𝑡𝑥) ∗ sin(2𝑡), where 𝑢1 = 𝑢 and 𝑢2 = 𝑣. Figure 4: Approximate solution of (5)-(8), for 𝛼(𝑡, 𝑥) = 2, where 𝑢1 = 𝑢 and 𝑢2 = 𝑣. behaviour of the solution is particularly interesting for the case 𝛼(𝑡, 𝑥) = 1.5 + 0.4 cos(𝑡𝑥) ∗ sin(2𝑡), see figure 6. Figure 5: Approximate solution of (5)-(8), for 𝛼(𝑡, 𝑥) = 1.35, where 𝑢1 = 𝑢 and 𝑢2 = 𝑣. Figure 6: Approximate solution of (5)-(8), for 𝛼(𝑡, 𝑥) = 1.5 + 0.4 cos(𝑡𝑥) sin(2𝑡), where 𝑢1 = 𝑢 and 𝑢2 = 𝑣. 7. Conclusions In this work, we have got interesting behavior of solutions for activator-inhibitor models with variable superdiffusion by replacing the classical second derivative in space by the variable order Riesz fractional derivative of order 1 < 𝛼(𝑡, 𝑥) ⩽ 2, it seems that our numerical results will open horizons for analytical studies about such types of models and guide them by guessing. References [1] S. B. Yuste, K. Lindenberg, Subdiffusion–limited reactions, Chemical physics 284 (2002) 169–180. doi:10.1016/S0301-0104(02)00546-3. [2] D. A. Benson, S. W. Wheatcraft, M. M. 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