Amplitudes of Composition Fluctuations in the Simplest Chemical Reaction Equilibrium

2004 ◽  
Vol 218 (9) ◽  
pp. 1033-1040 ◽  
Author(s):  
M. Šolc ◽  
J. Hostomský

AbstractWe present a numerical study of equilibrium composition fluctuations in a system where the reaction X1 ⇔ X2 having the equilibrium constant equal to 1 takes place. The total number of reacting particles is N. On a discrete time scale, the amplitude of a fluctuation having the lifetime 2r reaction events is defined as the difference between the number of particles X1 in the microstate most distant from the microstate N/2 visited at least once during the fluctuation lifetime, and the equilibrium number of particles X1, N/2. On the discrete time scale, the mean value of this amplitude, m̅(r̅), is calculated in the random walk approximation. On a continuous time scale, the average amplitude of fluctuations chosen randomly and regardless of their lifetime from an ensemble of fluctuations occurring within the time interval (0,z), z → ∞, tends with increasing N to ~1.243 N0.25. Introducing a fraction of fluctuation lifetime during which the composition of the system spends below the mean amplitude m̅(r̅), we obtain a value of the mean amplitude of equilibrium fluctuations on the continuous time scale equal to ~1.19√N. The results suggest that using the random walk value m̅(r̅) and taking into account a) the exponential density of fluctuations lifetimes and b) the fact that the time sequence of reaction events represents the Poisson process, we obtain values of fluctuations amplitudes which differ only slightly from those derived for the Ehrenfest model.

Psychometrika ◽  
2021 ◽  
Author(s):  
Oisín Ryan ◽  
Ellen L. Hamaker

AbstractNetwork analysis of ESM data has become popular in clinical psychology. In this approach, discrete-time (DT) vector auto-regressive (VAR) models define the network structure with centrality measures used to identify intervention targets. However, VAR models suffer from time-interval dependency. Continuous-time (CT) models have been suggested as an alternative but require a conceptual shift, implying that DT-VAR parameters reflect total rather than direct effects. In this paper, we propose and illustrate a CT network approach using CT-VAR models. We define a new network representation and develop centrality measures which inform intervention targeting. This methodology is illustrated with an ESM dataset.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Nikolaos Halidias

Abstract In this note we study the probability and the mean time for absorption for discrete time Markov chains. In particular, we are interested in estimating the mean time for absorption when absorption is not certain and connect it with some other known results. Computing a suitable probability generating function, we are able to estimate the mean time for absorption when absorption is not certain giving some applications concerning the random walk. Furthermore, we investigate the probability for a Markov chain to reach a set A before reach B generalizing this result for a sequence of sets A 1 , A 2 , … , A k {A_{1},A_{2},\dots,A_{k}} .


Mathematics ◽  
2021 ◽  
Vol 9 (8) ◽  
pp. 868
Author(s):  
Khrystyna Prysyazhnyk ◽  
Iryna Bazylevych ◽  
Ludmila Mitkova ◽  
Iryna Ivanochko

The homogeneous branching process with migration and continuous time is considered. We investigated the distribution of the period-life τ, i.e., the length of the time interval between the moment when the process is initiated by a positive number of particles and the moment when there are no individuals in the population for the first time. The probability generating function of the random process, which describes the behavior of the process within the period-life, was obtained. The boundary theorem for the period-life of the subcritical or critical branching process with migration was found.


1997 ◽  
Vol 29 (01) ◽  
pp. 92-113 ◽  
Author(s):  
Frank Ball ◽  
Sue Davies

The gating mechanism of a single ion channel is usually modelled by a continuous-time Markov chain with a finite state space. The state space is partitioned into two classes, termed ‘open’ and ‘closed’, and it is possible to observe only which class the process is in. In many experiments channel openings occur in bursts. This can be modelled by partitioning the closed states further into ‘short-lived’ and ‘long-lived’ closed states, and defining a burst of openings to be a succession of open sojourns separated by closed sojourns that are entirely within the short-lived closed states. There is also evidence that bursts of openings are themselves grouped together into clusters. This clustering of bursts can be described by the ratio of the variance Var (N(t)) to the mean[N(t)] of the number of bursts of openings commencing in (0, t]. In this paper two methods of determining Var (N(t))/[N(t)] and limt→∝Var (N(t))/[N(t)] are developed, the first via an embedded Markov renewal process and the second via an augmented continuous-time Markov chain. The theory is illustrated by a numerical study of a molecular stochastic model of the nicotinic acetylcholine receptor. Extensions to semi-Markov models of ion channel gating and the incorporation of time interval omission are briefly discussed.


2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Long Shi

In this work, a generalization of continuous time random walk is considered, where the waiting times among the subsequent jumps are power-law correlated with kernel function M(t)=tρ(ρ>-1). In a continuum limit, the correlated continuous time random walk converges in distribution a subordinated process. The mean square displacement of the proposed process is computed, which is of the form 〈x2(t)〉∝tH=t1/(1+ρ+1/α). The anomy exponent H varies from α to α/(1+α) when -1<ρ<0 and from α/(1+α) to 0 when ρ>0. The generalized diffusion equation of the process is also derived, which has a unified form for the above two cases.


1976 ◽  
Vol 13 (02) ◽  
pp. 219-230 ◽  
Author(s):  
J. Gani ◽  
I. W. Saunders

This paper is concerned with the parity of a population of yeast cells, each of which may bud, not bud or die. Two multitype models are considered: a Galton-Watson process in discrete time, and its analogous birth-death process in continuous time. The mean number of cells with parity 0, 1, 2, … is obtained in both cases; some simple results are also derived for the second moments of the two processes.


Paleobiology ◽  
2017 ◽  
Vol 43 (4) ◽  
pp. 667-692 ◽  
Author(s):  
Corentin Gibert ◽  
Gilles Escarguel

AbstractEstimating biodiversity and its variations through geologic time is a notoriously difficult task, due to several taphonomic and methodological effects that make the reconstructed signal potentially distinct from the unknown, original one. Through a simulation approach, we examine the effect of a major, surprisingly still understudied, source of potential disturbance: the effect of time discretization through biochronological construction, which generates spurious coexistences of taxa within discrete time intervals (i.e., biozones), and thus potentially makes continuous- and discrete-time biodiversity curves very different. Focusing on the taxonomic-richness dimension of biodiversity (including estimates of origination and extinction rates), our approach relies on generation of random continuous-time richness curves, which are then time-discretized to estimate the noise generated by this manipulation. A broad spectrum of data-set parameters (including average taxon longevity and biozone duration, total number of taxa, and simulated time interval) is evaluated through sensitivity analysis. We show that the deteriorating effect of time discretization on the richness signal depends highly on such parameters, most particularly on average biozone duration and taxonomic longevity because of their direct relationship with the number of false coexistences generated by time discretization. With several worst-case but realistic parameter combinations (e.g., when relatively short-lived taxa are analyzed in a long-ranging biozone framework), the original and time-discretized richness curves can ultimately show a very weak to zero correlation, making these two time series independent. Based on these simulation results, we propose a simple algorithm allowing the back-transformation of a discrete-time taxonomic-richness data set, as customarily constructed by paleontologists, into a continuous-time data set. We show that the reconstructed richness curve obtained this way fits the original signal much more closely, even when the parameter combination of the original data set is particularly adverse to an effective time-discretized reconstruction.


1998 ◽  
Vol 7 (4) ◽  
pp. 397-401 ◽  
Author(s):  
OLLE HÄGGSTRÖM

We consider continuous time random walks on a product graph G×H, where G is arbitrary and H consists of two vertices x and y linked by an edge. For any t>0 and any a, b∈V(G), we show that the random walk starting at (a, x) is more likely to have hit (b, x) than (b, y) by time t. This contrasts with the discrete time case and proves a conjecture of Bollobás and Brightwell. We also generalize the result to cases where H is either a complete graph on n vertices or a cycle on n vertices.


1981 ◽  
Vol 103 (4) ◽  
pp. 417-419 ◽  
Author(s):  
Bernard Friedland

The continuous-time Kalman filtering problem over a finite time interval can be made equivalent to a discrete-time filtering problem. The matrices in the latter are related to the submatrices of the transition matrix of a Hamiltonian system that corresponds to the continuous-time filtering problem.


2020 ◽  
Author(s):  
Oisín Ryan ◽  
Ellen Hamaker

Network analysis of ESM data has become popular in clinical psychology. In this approach, discrete-time (DT) vector autoregressive (VAR) models define the network structure with centrality measures used to identify intervention targets. However, VAR models suffer from time-interval dependency. Continuous Time (CT) models have been suggested as an alternative but require a conceptual shift, implying that DT-VAR parameters reflect total rather than direct effects. In this paper we propose and illustrate a CT network approach using CT-VAR models. We define a new network representation and develop centrality measures which inform intervention targeting. This methodology is illustrated with an ESM dataset.


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