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Research article Special Issues

Stability of thermoelastic Timoshenko system with variable delay in the internal feedback

  • Received: 21 February 2024 Revised: 13 May 2024 Accepted: 20 May 2024 Published: 28 May 2024
  • Based on the Fourier law of heat conduction, this paper was concerned with the thermoelastic Timoshenko system with memory and variable delay in the internal feedback, which describes the transverse vibration of a beam. By the Lummer-Phillips theorem and the variable norm technique suitable for the nonautonomous operator, the stability of the coupled system has been derived in space H.

    Citation: Xinfeng Ge, Keqin Su. Stability of thermoelastic Timoshenko system with variable delay in the internal feedback[J]. Electronic Research Archive, 2024, 32(5): 3457-3476. doi: 10.3934/era.2024160

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  • Based on the Fourier law of heat conduction, this paper was concerned with the thermoelastic Timoshenko system with memory and variable delay in the internal feedback, which describes the transverse vibration of a beam. By the Lummer-Phillips theorem and the variable norm technique suitable for the nonautonomous operator, the stability of the coupled system has been derived in space H.



    Dengue is an infectious illness that is spread in almost all countries, including in Indonesia [1]. Severe dengue is a prominent leader of critical disease and death in some Asian and Latin American countries. Every year, dengue cases occur in East Java province, Indonesia. Based on the Ministry of Health of the Republic of Indonesia, dengue cases in Indonesia until July 2020 reached 71,633. East Java is one of the provinces in Indonesia with high endemic potential from year to year [2].

    Dengue is a viral infection spread to humans through the bite of infected mosquitoes. Aedes aegypti mosquitoes are the major vectors that transmit the disease. The virus responsible for bringing dengue is called dengue virus (DENV). There are four DENV serotypes, and there is the potential to be infected four times. Currently, there is no particular treatment for dengue/severe dengue. Early detection of dengue disease progression and access to appropriate medical care reduce fatality rates of severe dengue to below 1%. Dengue prevention and regulation depends on effective vector control measures [1].

    Mathematical modeling can play essential roles in helping understand the complex phenomenon of epidemic spread including the malaria [3,4], tuberculosis [5,6], measles [7], meningitis [8], monkeypox [9], zika [10], and COVID-19 [11,12]. With a mathematical model, the relationship between the disease spread and epidemiological parameters can be identified. Several mathematical models of dengue transmission with various types compartments have been studied by researchers [13,14]. In [15,16], the authors designed mathematical model to study the effect of temperature on the spread of dengue fever. The impact of reinfection with the same serotype on the dynamics of dengue transmission has been studied in [17]. Researchers at [18,19] developed a fractional order model to understand the dynamics of dengue fever transmission. The authors in [20] presented a dynamical model of dengue with hospitalization to analyze the infection in East Java province, Indonesia. Ndii [21] formulated a dengue model by incorporating seasonally varying mosquitoes, vaccination, and media. The authors of [22] discussed a dengue model that accommodates releasing Wolbachia into wild mosquitoes and vaccination. The authors in [23] presented the dengue model by considering the recruitment rate of the human population in terms of logistic growth. The proposed model is more realistic because the growth rate of the human population is not always constant.

    This work aims to extend the previous study of [23] by formulating a dengue model that captures the control variables, such as fumigation and prevention, by applying the optimal control theory to the model. The model parameters will be estimated based on the dengue data in East Java Province, Indonesia. We employ efficiency and economic methods to examine the most cost-effective strategy among the implemented control scenarios. The remaining part of this paper proceeds as follows. Section 2 explains the model formulation. The analysis of the model is discussed in Section 3. The optimal control problem is studied in Section 4. Section 5 summarizes the main findings of this work.

    In this study, we consider the dengue transmission model with the assumption that the recruitment rate in the human population is logistic growth as proposed by [23]. The total human population (Nh) is divided into three sub-populations: the susceptible (Sh), the infectious (Ih), and the recovered (Rh). The total mosquitoes population (Nm) is divided into two sub-populations: the susceptible mosquitoes (Sm) and the infectious mosquitoes (Im). The flow diagram of the dengue model is displayed in Figure 1. As the diagram in Figure 1 shows, the dengue model is governed by an autonomous system of ODEs as follows:

    ddtSh=rNh(1NhK)(BβmhImNh+μh)Sh,ddtIh=BβmhImNhSh(ηh+μh)Ih,ddtRh=ηhIhμhRh,ddtSm=μmNm(BβhmIhNh+μm)Sm,ddtIm=BβhmIhNhSmμmIm, (2.1)

    with

    Nh=Sh+Ih+Rh

    and

    Nm=Sm+Im.
    Figure 1.  Transmission diagram of dengue model.

    The biologically feasible region of the model (2.1) is set out by

    Γ=ΓhΓmR3+×R2+, (2.2)

    where

    Γh={(Sh,Ih,Rh)R3+:NhK}

    and

    Γm={(Sm,Im)R2+:Sm+ImNm(0)}.

    The description of the variables and parameters of the dengue model can be set out in Tables 1 and 2, respectively.

    Table 1.  Descriptions of the model state variables.
    State variables Biological interpretation
    Sh The susceptible of the human population
    Ih The infectious of the human population
    Rh The recovery of human population
    Nh The total number of human population
    Sm The susceptible of the mosquito population
    Im The infectious of the mosquito population
    Nm The total number of the mosquito population

     | Show Table
    DownLoad: CSV
    Table 2.  Descriptions of model parameters.
    Symbol Description
    B The biting rate of mosquito
    βmh The transmission probability from Im to Sh
    βhm The transmission probability from Ih to Sm
    μh The natural death rate in human
    ηh The recovery rate in human
    μm The birth/death rate in the mosquito
    K Carrying capacity of the environment
    r Intrinsic growth rate

     | Show Table
    DownLoad: CSV

    The change rate of the total human population can be represented by

    dNhdt=[r(1NhK)μh]Nh.

    The total of the mosquito population is constant. Hence, the system (2.1) can be reduced into the following system:

    ddtNh=[r(1NhK)μh]Nh,ddtSh=rNh(1NhK)(BβmhImNh+μh)Sh,ddtIh=BβmhImNhSh(ηh+μh)Ih,ddtIm=BβhmIhNh(NmIm)μmIm. (2.3)

    In this present section, we devote the parameters estimation of the model (2.3) using the fitting least-squares method [24,25]. The monthly cumulative data of dengue in East Java Province, Indonesia, from 2018 until 2020 [26] is utilized in this study. The parameters μh, μm, and r are estimated taking the demographic information. The natural death rate of human (μh) is observed from inverse of the average lifespan in East Java Province. The average of lifespan in East Java Province from 2018 until 2020 is 71.15 years. Therefore,

    μh=171.15

    per year [27,28]. Next, the death rate of mosquito (μm), is found from the inverse of the average lifespan of Aedes mosquitoes. Based on [29], the average of lifespan of Aedes mosquitoes is 25 days, that is

    μm=125

    per day. Furthermore, for the growth rate of human (r), is obtained as follows. The average population in East Java Province from 2018 to 2020 is 39,955,059 [30]. Hence,

    rμh=39,955,059,

    which is the total human population without the disease, so that r= 561,560.91 per year. The other parameters, such as B,  βmh,  βhm,  ηh,  K, and Nm, are estimated with the objective function that minimize

    minB, βmh, βhm, ηh, K, Nmtfi=0(IiIdatai)2 ,

    where tf is the end time of the cumulative dengue cases data Idatai and Ii, (i=0, 1, 2,, tf) are the cumulative numerical solutions of infected humans from system (2.3). Thus, the initial populations are

    (Nh0,Sh0,Ih0,Im0)=(39,500,851,Nh0Ih0,Idata0, 100),

    while the initial parameter values for estimation are

    (B0,βmh0,βhm0,ηh0,K0,Nm0)=(0.4,0.4,0.4,0.4,1.5Nh0,2.5Nh0).

    The lower bound parameter values are (103, 103, 103, 103, 1.2Nh0, 2Nh0) and upper bound parameter values are (1, 1, 1, 1, 2Nh0, 3Nh0). The result of the estimation and parameter value can be seen in Figure 2 and Table 3.

    Figure 2.  Comparison of dengue data and the model.
    Table 3.  The parameter value of the model.
    Parameter Value (months) Source
    B 0.3848 Fitted
    βmh 0.3632 Fitted
    βhm 0.3252 Fitted
    μh 11271.15 Estimated
    ηh 0.0198 Fitted
    μm 11225365 Estimated
    K 59,229,000 Fitted
    r 39,955,0591271.15 Estimated
    Nm 98,782,000 Fitted

     | Show Table
    DownLoad: CSV

    In this section, we present the equilibria and the local stability of the DHF model.

    Model (2.3) has the dynamic characteristic of model (2.1), so to understand the dynamics behaviour of the model (2.1), we carry out the analysis of the model (2.3). Likewise, the biological domain in both models is the same. Based on [23], two equilibria are obtained, namely the disease-free equilibrium (DFE) and the endemic equilibrium. The DFE of the system (2.3) is provided by

    E0(Nh,Sh,0,0)=(K(1μhr),K(1μhr),0,0).

    The DFE E0 is exist if r>μh.

    Meanwhile, the endemic equilibrium is

    E1(Nh,Sh,Ih,Im)=(˜Nh,˜Sh,˜Ih,˜Im)

    with

    ˜Nh=K(1μhr),˜Sh=(ηh+μh)˜Nh(Bβhm˜Ih+μm˜Nh)B2βmhβhmNm,˜Ih=μh(B2βmhβhmNmμm(ηh+μh)˜Nh)Bβhm(ηh+μh)(BβmhNm˜Nh+μh),˜Im=BβhmNm˜IhBβhm˜Ih+μm˜Nh.

    The endemic equilibrium exists if

    B2βmhβhmNmμm(ηh+μh)˜Nh>1

    or

    B2βmhβhmNmμm(ηh+μh)K(1μhr)>1,r>μh.

    Using the the next-generation matrix method [31], we yield the basic reproduction number as follows:

    R0=B2βhmβmhNmμmK(1μhr)(ηh+μh),r>μh. (3.1)

    By using the formulation of R0, the endemic equilibrium exists if

    R20=B2βmhβhmNmμm(ηh+μh)K(1μhr)>1

    or R0>1 and r>μh.

    The local stability analysis of dengue model (2.3) can be expressed by the following theorem.

    Theorem 3.1. The diseases-free equilibrium E0(Nh,Sh,0,0) of the model (2.3) is locally asymptotically stable if

    R0<1.

    Proof. The evaluation of Jacobian matrix of the system (2.3) at DFE E0, we have

    JE0=(μhr0002μhrμh0Bβmh00(ηh+μh)Bβmh00BβmhNmK(1μhr)μm). (3.2)

    The two eigenvalues of Jacobian matrix (3.2) are μh,(rμh) that are obviously negative. The other two remaining eigenvalues can be found through the following characteristics equation:

    λ2+a1λ+a2=0 (3.3)

    for

    a1=(μm+ηh+μh)

    and

    a2=(ηh+μh)μmB2βmhβhmNmK(1μhr).

    Using Routh-Hurwitz criterion, the roots of the Eq (3.3) are negative if a1,a2>0. The coefficient a1>0, while a2>0 if

    B2βmhβhmNmμm(ηh+μh)K(1μhr)<1

    or

    R0<1.

    So, the theorem is proven.

    The endemic equilibrium E1 in model (2.3) will be asymptotically stable if

    R0>1.

    By Substituting the endemic equilibrium E1 to Jacobian matrix of the system (2.3), we find that the eigenvalue is (rμh) and the others are the roots of the equation

    λ3+[Bβmh˜Nh(˜Im+˜Ih)+2μh+μm+ηh]λ2+[(Bβmh˜Im˜Nh+μh)(Bβhm˜Ih˜Nh+μm+ηh+μh)+(ηh+μh)(Bβhm˜Ih˜Nh+μm)B2βmhβhm˜Sh˜N2h(Nm˜Im)]λ+(Bβmh˜Im˜Nh+μh)[(ηh+μh)(Bβhm˜Ih˜Nh+μm)B2βmhβhm˜Sh˜N2h(Nm˜Im)]+B3β2mhβhm˜Ih˜Sh˜N3h(Nm˜Im)=0. (3.4)

    Equation (3.4) can be expressed by

    λ3+b1λ2+b2λ+b3=0

    with

    b1=Bβmh˜Nh(˜Im+˜Ih)+2μh+μm+ηh,b2=(Bβmh˜Im˜Nh+μh)(Bβhm˜Ih˜Nh+μm+ηh+μh)+(ηh+μh)(Bβhm˜Ih˜Nh+μm)B2βmhβhm˜Sh˜N2h(Nm˜Im),b3=(Bβmh˜Im˜Nh+μh)[(ηh+μh)(Bβhm˜Ih˜Nh+μm)][B2βmhβhm˜Sh˜N2h(Nm˜Im)]+B3β2mhβhm˜Ih˜Sh˜N3h(Nm˜Im).

    According to the Ruth-Hurwitz criteria, the roots of the characteristic equation will be negative or have a negative real part if

    b1,b2,b3>0

    and

    b1b2b3>0.

    The coefficients b1b3 containing ˜Nh,˜Sh,˜Ih,˜Im so showing that the condition for the root must be positive will be difficult to do analytically. Therefore, the numerical simulation is implemented to analyze the stability of the endemic equilibrium. The parameter values used are given in Table 3.

    The phase plane graph between the infected mosquito population and the infected human population is presented in Figure 3. Based on Figure 3, it can be seen that the three graphs converges to the endemic equilibrium E1 as time evolves when

    R0>1.
    Figure 3.  Phase field of (Im) and (Ih).

    In this work, we discuss the sensitivity analysis to recognize the parameter that can influence the threshold R0. To assign the sensitivity index, we refer to [32]. The calculation of the sensitivity index R0 towards to some parameter, say a, is given by

    ΥR0a=R0a×aR0.

    Using the parameter values in Table 3, the sensitivity indexes of R0 are summarized in Table 4.

    Table 4.  Sensitivity index of the parameters.
    Parameter Sensitivity index
    B 1
    βmh 0.5
    βhm 0.5
    μh 0.028
    ηh 0.472
    μm 0.5
    K 0.5
    r 1.266×108
    Nm 0.5

     | Show Table
    DownLoad: CSV

    The interpretation of the sensitivity index in Table 4 can be explained as follows. The positive sign reveals that when the parameter values are raised, the value of R0 will also increase. Conversely, the negative sign reveals that when the parameter's value is raised, the value of R0 will be decreased. For example, for

    ΥR0B=1,

    increasing the value of the biting rate of mosquito by 10%, causes R0 to increase by 10%. Thus, for

    ΥR0K=0.5,

    increasing the carrying capacity by 10%, causes R0 to decrease by 5%. Likewise, for the other indexes. The highly sensitive parameters should be considered carefully because small variations in these parameters will cause large quantitative changes. Table 4 shows that the parameter with the greatest influence on the threshold is parameter B. The implication is that an increase in the value of the biting rate of mosquitoes increases the spread of dengue disease in the population. Hence, we can anticipate it with preventive control by using a bed net and mosquito repellent lotion or fumigation control to reduce the mosquito population. Furthermore, the value of the biting rate of mosquitoes will decrease, which implies dengue transmission in the community also decreases.

    Based on the contour plot in Figures 4 and 5, the basic reproduction number (R0) will increase in proportion to the results of the sensitivity analysis in Table 4. The parameters B and βmh have a positive relation; however the parameters μm and ηh have a negative relation.

    Figure 4.  The behaviour of R0 to the parameters μm and B.
    Figure 5.  The behaviour of R0 to the parameters βmh and ηh.

    In this section, we apply the optimal control (OC) strategy to the dengue model. Based on the sensitivity analysis in the previous section, we can reduce the number of mosquito biting rates with fumigation and prevention efforts. Therefore, we define two control variables, namely u1 as fumigation and u2 as prevention. The dengue model with control variables can be written as follows

    dShdt=rNh(1NhK)(1u2)BβmhImNhShμhSh,dIhdt=(1u2)BβmhImNhSh(ηh+μh)Ih,dRhdt=ηhIhμhRh,dSmdt=μmNmBβhmIhNhSmμmSmκu1Sm,dImdt=BβhmIhNhSmμmImκu1Im.

    The control variables u1 and u2 are established on interval [0,tf], where

    0ui(t)1,   t[0,tf],   i=1,2,

    and tf represent the final time of the controls. We aim to minimize the number of infected human populations and mosquito populations and keep the cost of employing fumigation and prevention controls as low as possible. For this, we state the objective function

    J(u1,u2)=tf0(A1Ih+A2Im+12c1u21+12c2u22)dt,

    where A1 and A2 are weights of the objective function for Ih and Im, respectively, and c1, and c2 are weight parameters for fumigation and prevention respectively. We utilize the quadratic cost function for J to depict the cost of control efforts. This quadratic function can explain a nonlinear cost increase associated with the performance of control attempts in the field [33,34].

    Then, to solve this optimal control problem, we assumed that Nh is constant. Using Pontryagin's maximum principle [35], the optimal solutions of u1 and u2 are provided by

    u1=min{1,max(0,κ(λ4Sm+λ5Imc1)) } ,u2=min{1,max(0,(λ2λ1)BβmhImc2NhSh) } .

    The variables λi, i=1,2,3,4,5, are represented as adjoint variables or co-state which satisfies the following equations

    dλ1dt=(λ1λ2)(1u2)BβmhImNh+λ1μh,dλ2dt=A1+(λ2λ3)ηh+(λ4λ5)BβhmSmNh+λ2μh,dλ3dt=λ3μh,dλ4dt=(λ4λ5)BβhmIhNh+λ4(μm+κu1),dλ5dt=A2+(λ1λ2)(1u2)BβmhShNh+λ5(μm+κu1),

    where the transversality conditions

    λi(tf)=0,   i=1,2,3,4,5.

    In this optimal control problem, because Nh is assumed to be constant,

    dNhdt=0 r=KKNhμh,

    as Nh is the population in East Java Province in 2018. We assume that the values of the parameters are given by

    A1=A2=1,  c1=15,  c2=10,  κ=0.7

    and

    r=KKNhμh

    and the other parameters are referred to Table 3. We solve the numerical optimal control simulation using the backward and forward iteration technique as stated in [36]. To determine which strategy or combination provides useful methods of controlling dengue, we addressed the following strategies for our simulation result, as enumerated below.

    The result of the simulation of comparison Ih and Im without and with control when fumigation usage only is given in Figure 6. We can observe that using this strategy, the infections of humans and mosquitoes tend to decrease compared to no control. The profile of the optimal control u1 only is presented in Figure 7. It is apparent that fumigation control should be carried out intensively for a maximum of 50 months.

    Figure 6.  Comparison Ih and Im without and with control.
    Figure 7.  Control profile of u1.

    The result of the simulation of comparison Ih and Im without and with control when prevention usage only is given in Figure 8. From Figure 8, it can be seen that both infection of humans and mosquitoes significantly reduce using this strategy. The profile of the optimal control u2 only is displayed in Figure 9. This figure shows that prevention control should be provided with full effort for almost 50 months.

    Figure 8.  Comparison Ih and Im without and with control.
    Figure 9.  Control profile of u2.

    The result of the simulation of comparison Ih and Im without and with control when implementing both fumigation and prevention are given in Figure 10.

    Figure 10.  Comparison Ih and Im without and with controls.

    Using the last strategy, it is found that both infectious humans and mosquitoes diminish over to compare to without controls. The profile of the optimal control u1 and u2 simultaneously is demonstrated in Figure 11. As depicted in Figure 11, we found that fumigation and preventive control were both maintaining at maximum levels for nearly 50 months before decaying gradually to the lower bound.

    Figure 11.  Control profiles of u1 and u2 simultaneously.

    Furthermore, to evaluate the most proper strategy, we assess and compare the merit and the costs related to the control measures by adopting the infection averted ratio (IAR), average cost-effectiveness ratio (ACER) and incremental cost-effectiveness ratio (ICER). These economic verify are mathematically established in [37,38] as follows:

    IAR=Cumulative infected avertedCumulative recovered.

    The cumulative infected averted is presented by the sum of the difference between the total infectious individuals without and with control. More explicitly

    IAR=tf0(Ih(t)Ih(t)) dttf0Rh(t) dt,

    where the symbol with subscript is employed to represent the optimal solutions associated with the corresponding strategy. The most powerful strategy when taking IAR is the strategy with the highest ratio

    ACER=Total cost invested on the interventionTotal number of infectious averted.

    It proposes a single intervention and evaluates it against its baseline desire. The aim of fumigation control (u1) is the reduction of mosquitoes, while prevention control (u2) is to protect susceptible humans by diminishing the contact rate. Therefore, we deal with

    ACER=tf0(C1u1(t)Nm(t)+C2u2(t)Sh(t)) dttf0(Ih(t)Ih(t)) dt,

    where Ci represents the cost of the 2 possible interventions. The most cost-effective strategy when using ACER is the strategy with the smallest ratio.

    ICER=Difference in cost produced by strategies i and jDifference in the total of infections averted in strategies i and j.

    Hence, ICER is utilized to compare two different strategies, namely i and j. We calculate the cost of a strategy as undertaken for ACER. When comparing two or more competing intervention strategies incrementally, one intervention is compared with the next effective alternative in increasing order of total infected averted [37]. In computing ACER and ICER, we address the same cost for both interventions

    C1=C2=1.

    The result of the calculation of the total infection and total cost is summarised in Table 5, while IAR and ACER is set out in Table 6.

    Table 5.  Total cost for each intervention strategy.
    Strategies Total Infection averted Total cost
    1 3.112406×104 3.1460×109
    3 4.394527×104 5.0813×109
    2 4.394682×104 1.9622×109

     | Show Table
    DownLoad: CSV
    Table 6.  Comparison of IAR and ACER for each intervention strategy.
    Strategies IAR ACER
    1 1.2901 1.0108×105
    3 2.2588 1.1563×105
    2 2.2589 4.4650×104

     | Show Table
    DownLoad: CSV

    Based on Table 5, Strategy 2 averts the greatest number of infections and yields the largest ratio

    IAR=2.2589.

    Hence, it is the most effective. This strategy is also the most cost-effective because it is associated with the smallest average cost-effectiveness ratio

    ACER=4.4650×104.

    Using the total infection and total cost in Table 5, the ICER indexes, as summarised in Table 7, are computed as follows:

    ICER(1)=3.1460×10903.112406×1040=1.0108×105,ICER(2)=1.9622×1095.0813×1094.394682×1044.394527×104=2.0123×109,ICER(3)=5.0813×1093.1460×1094.394527×1043.112406×104=1.5095×105.
    Table 7.  Comparison of ICER for each intervention strategy.
    Strategies ICER ICER recalculated
    1 1.0108×105 1.8917×104
    3 1.5095×105 -
    2 2.0123×109 0.9232×105

     | Show Table
    DownLoad: CSV

    Comparing Strategies 1 and 3, the utilization of Strategy 1 is cost-saving over Strategy 3. This means that Strategy 3 is less effective and more costly than the other strategy. Hence, Strategy 3 is eliminated. Furthermore, we recalculate the index of ICER as follows:

    ICER(1)=3.1460×10903.112406×1040=1.0108×105,ICER(2)=1.9622×1093.1460×1094.394682×1043.112406×104=0.9232×105.

    Comparing Strategies 1 and 2, the application of Strategy 2 is cost-saving over Strategy 1. This indicates that Strategy 1 is less effective and more costly than the other strategy. Hence, Strategy 1 is removed. Our results recommend that Strategy 2 is the most cost-effective intervention associated with the ICER.

    This study has investigated the dengue model by incorporating the logistic growth on the recruitment rate in the human population. The model analyses exhibited that the disease-free equilibrium is locally stable when the reproduction number is less than one, while the endemic equilibrium tends to be asymptotically stable when the threshold is greater than one. The parameters of the dengue model are estimated using data on cases of dengue in East Java Province, Indonesia, from 2018 to 2020. The findings indicate that the spread of dengue is persistent in the population.

    Next, the sensitivity analysis shows that mosquito biting rate is the most influential parameter in the spread of dengue. Therefore, we carried out the control strategy in the form of fumigation and prevention. Pontryagin's maximum principle was adopted to accomplish the optimal control that minimizes the spread of dengue. The results of the optimal control problem show that the spread of dengue can be controlled by implementing sustainable control over a short period of time, which shows that the optimal control strategy is effective on humans and mosquitoes. Based on the cost-effectiveness evaluation, prevention is the most effective step to reduce dengue transmission using IAR, ACER, and ICER cost analysis.

    The authors declare they have not used Artificial Intelligence (AI) tools in the creation of this article.

    This research has been supported by the Ministry of Research, Technology and Higher Education, Republic of Indonesia, through the PDD 2020.

    All authors declare that they have no conflicts of interest in this paper.



    [1] S. P. Timoshenke, On the correction for shear of the differential equation for transverse vibrations of prismatic bars, Philos. Mag., 41 (1921), 744–746. https://doi.org/10.1080/14786442108636264 doi: 10.1080/14786442108636264
    [2] J. E. M. Rivera, R. Racke, Global stability for damped Timoshenko systems, Discrete Contin. Dyn. Syst., 9 (2003), 1625–1639. https://doi.org/10.3934/dcds.2003.9.1625 doi: 10.3934/dcds.2003.9.1625
    [3] J. E. M. Rivera, R. Racke, Timoshenko systems with indefinite damping, J. Math. Anal. Appl., 341 (2008), 1068–1083. https://doi.org/10.1016/j.jmaa.2007.11.012 doi: 10.1016/j.jmaa.2007.11.012
    [4] M. I. Mustafa, S. A. Messaoudi, General energy decay rates for a weakly damped Timoshenko system, J. Dyn. Control Syst., 16 (2010), 211–226. https://doi.org/10.1007/s10883-010-9090-z doi: 10.1007/s10883-010-9090-z
    [5] D. S. A. Jnior, M. L. Santos, J. E. M. Rivera, Stability to 1-D thermoelastic Timoshenko beam acting on shear force, Z. Angew. Math. Phys., 65 (2014), 1233–1249. https://doi.org/10.1007/s00033-013-0387-0 doi: 10.1007/s00033-013-0387-0
    [6] M. O. Alves, A. H. Caixeta, M. A. J. Silva, J. H. Rodrigues, D. S. A. Junior, On a Timoshenko system with thermal coupling on both the bending moment and the shear force, J. Evol. Equations, 20 (2020), 295–320. https://doi.org/10.1007/s00028-019-00522-8 doi: 10.1007/s00028-019-00522-8
    [7] M. O. Alves, E. H. G. Tavares, M. A. J. Silva, J. H. Rodrigues, On modeling and uniform stability of a partially dissipative viscoelastic Timoshenko system, SIAM J. Math. Anal., 51 (2019), 4520–4543. https://doi.org/10.1137/18M1191774 doi: 10.1137/18M1191774
    [8] M. S. Alves, M. A. J. Silva, T. F. Ma, J. E. M. Rivera, Invariance of decay rate with respect to boundary conditions in thermoelastic Timoshenko systems, Z. Angew. Math. Phys., 67 (2016), 70. https://doi.org/10.1007/s00033-016-0662-y doi: 10.1007/s00033-016-0662-y
    [9] M. S. Alves, M. A. J. Silva, T. F. Ma, J. E. M. Rivera, Non-homogeneous thermoelastic Timoshenko systems, Bull. Braz. Math. Soc., 48 (2017), 461–484. https://doi.org/10.1007/s00574-017-0030-3 doi: 10.1007/s00574-017-0030-3
    [10] L. H. Fatori, R. N. Monteiro, H. D. F. Sare, The Timoshenko system with history and Cattaneo law, Appl. Math. Comput., 228 (2014), 128–140. https://doi.org/10.1016/j.amc.2013.11.054 doi: 10.1016/j.amc.2013.11.054
    [11] J. E. M. Rivera, R. Racke, Mildly dissipative nonlinear Timoshenko systems-global existence and exponential stability, J. Math. Anal. Appl., 276 (2002), 248–278. https://doi.org/10.1016/S0022-247X(02)00436-5 doi: 10.1016/S0022-247X(02)00436-5
    [12] M. L. Santos, D. S. A. Jnior, J. E. M. Rivera, The stability number of the Timoshenko system with second sound, J. Differ. Equations, 253 (2012), 2715–2733. https://doi.org/10.1016/j.jde.2012.07.012 doi: 10.1016/j.jde.2012.07.012
    [13] H. D. F. Sare, R. Racke, On the stability of damped Timoshenko systems: Cattaneo versus Fourier law, Arch. Ration. Mech. Anal., 194 (2009), 221–251. https://doi.org/10.1007/s00205-009-0220-2 doi: 10.1007/s00205-009-0220-2
    [14] M. A. J. Silva, R. Racke, Effect of history and heat models on the staility of thermoelastic Timoshenko systems, J. Differ. Equations, 275 (2021), 167–203. https://doi.org/10.1016/j.jde.2020.11.041 doi: 10.1016/j.jde.2020.11.041
    [15] F. Ammar-Khodja, S. Kerbal, A. Soufyane, Stabilization of the nonuniform Timoshenko beam, J. Math. Anal. Appl., 327 (2007), 525–538. https://doi.org/10.1016/j.jmaa.2006.04.016 doi: 10.1016/j.jmaa.2006.04.016
    [16] H. D. F. Sare, J. E. M. Rivera, Exponential decay of Timoshenko system with indefinite memory dissipation, Adv. Differ. Equations, 13 (2008), 733–752. https://doi.org/10.57262/ade/1355867334 doi: 10.57262/ade/1355867334
    [17] Z. Ma, L. Zhang, X. Yang, Exponential stability for a Timoshenko-type system with history, J. Math. Anal. Appl., 380 (2011), 299–312. https://doi.org/10.1016/j.jmaa.2011.02.078 doi: 10.1016/j.jmaa.2011.02.078
    [18] J. E. M. Rivera, H. D. F. Sare, Stability of Timoshenko systems with past history, J. Math. Anal. Appl., 339 (2008), 482–502. https://doi.org/10.1016/j.jmaa.2007.07.012 doi: 10.1016/j.jmaa.2007.07.012
    [19] T. Caraballo, J. Real, Attractors for 2D Navier-Stokes models with delays, J. Differ. Equations, 205 (2004), 271–297. https://doi.org/10.1016/j.jde.2004.04.012 doi: 10.1016/j.jde.2004.04.012
    [20] J. M. G. Luengo, P. M. Rubio, G. Planas, Attractors for a double time-delayed 2D-Navier-Stokes model, Discrete Contin. Dyn. Syst. - Ser. A, 34 (2014), 4085–4105. Available from: http://hdl.handle.net/11441/25923.
    [21] X. Yang, L. Li, X. Yan, L. Ding, The structure and stability of pullback attractors for 3D Brinkman-Forchheimer equation with delay, Electron. Res. Arch., 28 (2020), 1395–1418. https://doi.org/10.3934/era.2020074 doi: 10.3934/era.2020074
    [22] B. Feng, M. L. Pelicer, Global existence and exponential stability for a nonlinear Timoshenko system with delay, Boundary Value Probl., 2015 (2015), 206. https://doi.org/10.1186/s13661-015-0468-4 doi: 10.1186/s13661-015-0468-4
    [23] B. Feng, X. Yang, Long-time dynamics for a nonlinear Timoshenko system with delay, Appl. Anal., 96 (2017), 606–625. https://doi.org/10.1080/00036811.2016.1148139 doi: 10.1080/00036811.2016.1148139
    [24] X. Yang, J. Zhang, Y. Lu, Dynamics of the nonlinear Timoshenko system with variable delay, Appl. Math. Optim., 83 (2021), 297–326. https://doi.org/10.1007/s00245-018-9539-0 doi: 10.1007/s00245-018-9539-0
    [25] Z. Liu, S. Zheng, Semigroups Associated with Dissipative Systems, Chapman and Hall/CRC, 1999.
    [26] T. Kato, Linear and quasi-linear equations of evolution of hyperbolic type, in Hyperbolicity, (2011), 125–191. https://doi.org/10.1007/978-3-642-11105-1_4
    [27] M. Hu, X. Yang, J. Yuan, Stability and dynamics for Lamˊe system with degenerate memory and time-varying delay, Appl. Math. Optim., 89 (2024), 14. https://doi.org/10.1007/s00245-023-10080-8 doi: 10.1007/s00245-023-10080-8
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