No Arabic abstract
We consider the chemical reaction networks and study currents in these systems. Reviewing recent decomposition of rate functionals from large deviation theory for Markov processes, we adapt these results for reaction networks. In particular, we state a suitable generalisation of orthogonality of forces in these systems, and derive an inequality that bounds the free energy loss and Fisher information by the rate functional.
We continue the investigation, started in [J. Stat. Phys. 166, 926-1015 (2017)], of a network of harmonic oscillators driven out of thermal equilibrium by heat reservoirs. We study the statistics of the fluctuations of the heat fluxes flowing between the network and the reservoirs in the nonequilibrium steady state and in the large time limit. We prove a large deviation principle for these fluctuations and derive the fluctuation relation satisfied by the associated rate function.
The Greens function method which has been originally proposed for linear systems has several extensions to the case of nonlinear equations. A recent extension has been proposed to deal with certain applications in quantum field theory. The general solution of second order nonlinear differential equations is represented in terms of a so-called short time expansion. The first term of the expansion has been shown to be an efficient approximation of the solution for small values of the state variable. The proceeding terms contribute to the error correction. This paper is devoted to extension of the short time expansion solution to non-linearities depending on the first derivative of the unknown function. Under a proper assumption on the nonlinear term, a general representation for Greens function is derived. It is also shown how the knowledge of nonlinear Greens function can be used to study the spectrum of the nonlinear operator. Particular cases and their numerical analysis support the advantage of the method. The technique we discuss grants to obtain a closed form analytic solution for non-homogeneous non-linear PDEs so far amenable just to numerical solutions. This opens up the possibility of several applications in physics and engineering.
In this paper we study some classes of second order non-homogeneous nonlinear differential equations allowing a specific representation for nonlinear Greens function. In particular, we show that if the nonlinear term possesses a special multiplicativity property, then its Greens function is represented as the product of the Heaviside function and the general solution of the corresponding homogeneous equations subject to non-homogeneous Cauchy conditions. Hierarchies of specific non-linearities admitting this representation are derived. The nonlinear Greens function solution is numerically justified for the sinh-Gordon and Liouville equations. We also list two open problems leading to a more thorough characterizations of non-linearities admitting the obtained representation for the nonlinear Greens function.
We consider stochastic models of chemical reaction networks with time dependent input rates and several types of molecules. We prove that, in despite of strong time dependence of input rates, there is a kind of homeostasis phenomenon: far away from input nodes the mean numbers of molecules of each type become approximately constant (do not depend on time).
In a previous work we devised a framework to derive generalised gradient systems for an evolution equation from the large deviations of an underlying microscopic system, in the spirit of the Onsager-Machlup relations. Of particular interest is the case where the microscopic system consists of random particles, and the macroscopic quantity is the empirical measure or concentration. In this work we take the particle flux as the macroscopic quantity, which is related to the concentration via a continuity equation. By a similar argument the large deviations can induce a generalised gradient or Generic system in the space of fluxes. In a general setting we study how flux gradient or generic systems are related to gradient systems of concentrations. The arguments are explained by the example of reacting particle systems, which is later expanded to include spatial diffusion as well.