We consider an extreme renewal process with no-mean heavy-tailed Pareto(II) inter-renewals and shape parameter $\alpha$ where $0\lt\alpha \leq 1$. Two steps are required to derive integral expressions for the analytic probability density functions (pdfs) of the fixed finite time $t$ excess, age, and total life, and require extensive computations. Step 1 creates and solves a Volterra integral equation of the second kind for the limiting pdf of a basic underlying regenerative process defined in the text, which is used for all three fixed finite time $t$ pdfs. Step 2 builds the aforementioned integral expressions based on the limiting pdf in the basic underlying regenerative process. The limiting pdfs of the fixed finite time $t$ pdfs as $t\rightarrow \infty$ do not exist. To reasonably observe the large $t$ pdfs in the extreme renewal process, we approximate them using the limiting pdfs having simple well-known formulas, in a companion renewal process where inter-renewals are right-truncated Pareto(II) variates with finite mean; this does not involve any computations. The distance between the approximating limiting pdfs and the analytic fixed finite time large $t$ pdfs is given by an $L_{1}$ metric taking values in $(0,1)$, where “near $0$” means “close” and “near $1$” means “far”.

A class of controlled branching processes with continuous time is introduced and some limiting distributions are obtained in the critical case. An extension of this class as regenerative controlled branching processes with continuous time is proposed and some asymptotic properties are considered.

Let (Mt:t>0) be a Markov process of tessellations of ℝℓ, and let (𝒞t:t>0) be the process of their zero cells (zero polytopes), which has the same distribution as the corresponding process for Poisson hyperplane tessellations. In the present paper we describe the stationary zero cell process (at𝒞at:t∈ℝ),a>1, in terms of some regenerative structure and we show that it is a Bernoulli flow. An important application is to STIT tessellation processes.

In this paper we estimate quantile sensitivities for dependent sequences via infinitesimal perturbation analysis, and prove asymptotic unbiasedness, weak consistency, and a central limit theorem for the estimators under some mild conditions. Two common cases, the regenerative setting and ϕ-mixing, are analyzed further, and a new batched estimator is constructed based on regenerative cycles for regenerative processes. Two numerical examples, the G/G/1 queue and the Ornstein–Uhlenbeck process, are given to show the effectiveness of the estimator.

Let I be a finite set and S be a nonempty strict subset of I which is partitioned into classes, and let C(s) be the class containing s ∈ S. Let (Ps: s ∈ S) be a family of distributions on IN, where each Ps applies to sequences starting with the symbol s. To this family, we associate a class of distributions P(π) on IN which depends on a probability vector π. Our main results assume that, for each s ∈ S, Ps regenerates with distribution Ps' when it encounters s' ∈ S ∖ C(s). From semiregenerative theory, we determine a simple condition on π for P(π) to be time stationary. We give a similar result for the following more complex model. Once a symbol s' ∈ S ∖ C(s) has been encountered, there is a decision to be made: either a new region of type C(s') governed by Ps' starts or the region continues to be a C(s) region. This decision is modeled as a random event and its probability depends on s and s'. The aim in studying these kinds of models is to attain a deeper statistical understanding of bacterial DNA sequences. Here I is the set of codons and the classes (C(s): s ∈ S) identify codons that initiate similar genomic regions. In particular, there are two classes corresponding to the start and stop codons which delimit coding and noncoding regions in bacterial DNA sequences. In addition, the random decision to continue the current region or begin a new region of a different class reflects the well-known fact that not every appearance of a start codon marks the beginning of a new coding region.

Let {Zn}n≥0 be a random walk with a negative drift and independent and identically distributed increments with heavy-tailed distribution, and let M = supn≥0Zn be its supremum. Asmussen and Klüppelberg (1996) considered the behavior of the random walk given that M > x for large x, and obtained a limit theorem, as x → ∞, for the distribution of the quadruple that includes the time τ = τ(x) to exceed level x, position Zτ at this time, position Zτ-1 at the prior time, and the trajectory up to it (similar results were obtained for the Cramér-Lundberg insurance risk process). We obtain here several extensions of this result to various regenerative-type models and, in particular, to the case of a random walk with dependent increments. Particular attention is given to describing the limiting conditional behavior of τ. The class of models includes Markov-modulated models as particular cases. We also study fluid models, the Björk-Grandell risk process, give examples where the order of τ is genuinely different from the random walk case, and discuss which growth rates are possible. Our proofs are purely probabilistic and are based on results and ideas from Asmussen, Schmidli and Schmidt (1999), Foss and Zachary (2002), and Foss, Konstantopoulos and Zachary (2007).

Many regenerative arguments in stochastic processes use random times which are akin to stopping times, but which are determined by the future as well as the past behaviour of the process of interest. Such arguments based on ‘conditioning on the future’ are usually developed in an ad-hoc way in the context of the application under consideration, thereby obscuring the underlying structure. In this paper we give a simple, unified, and more general treatment of such conditioning theory. We further give a number of novel applications to various particle system models, in particular to various flavours of contact processes and to infinite-bin models. We give a number of new results for existing and new models. We further make connections with the theory of Harris ergodicity.

This paper provides a simple proof for the fact that the hitting time to an infrequently visited subset for a one-dependent regenerative process converges weakly to an exponential distribution. Special cases are positive recurrent Harris chains and Harris processes. The paper further extends this class of limit theorems to ‘rewards’ that are cumulated to the hitting time of such a rare set.

In this paper, we obtain a closed form for the covariance function of a general stationary regenerative process. It is used to derive exact asymptotics of the covariance function of stationary ON/OFF and workload processes, when ON and OFF periods are heavy-tailed and mutually dependent. The case of a G/G/1/0 queueing system with heavy-tailed arrival and/or service times is studied in detail.

We give precise asymptotic estimates of the tail behavior of the distribution of the supremum of a process with regenerative increments. Our results cover four qualitatively different regimes involving both light tails and heavy tails, and are illustrated with examples arising in queueing theory and insurance risk.

We generalize a theorem due to Keilson on the approximate exponentiality of waiting times for rare events in regenerative processes. We use the result to investigate the limit distribution for a family of first entrance times in a sequence of Ehrenfest urn models. As a second application, we consider approximate pattern matching, a problem arising in molecular biology and other areas.

Let (Yn, Nn)n≥1 be independent and identically distributed bivariate random variables such that the Nn are positive with finite mean ν and the Yn have a common heavy-tailed distribution F. We consider the process (Zn)n≥1 defined by Zn = Yn - Σn-1, where It is shown that the probability that the maximum M = maxn≥1Zn exceeds x is approximately as x → ∞, where F' := 1 - F. Then we study the integrated tail of the maximum of a random walk with long-tailed increments and negative drift over the interval [0, σ], defined by some stopping time σ, in the case in which the randomly stopped sum is negative. Finally, an application to risk theory is considered.

We consider an infinite capacity buffer where the incoming fluid traffic belongs to K different types modulated by K independent Markovian on-off processes. The kth input process is described by three parameters: (λk, μk, rk), where 1/λk is the mean off time, 1/μk is the mean on time, and rk is the constant peak rate during the on time. The buffer empties the fluid at rate c according to a first come first served (FCFS) discipline. The output process of type k fluid is neither Markovian, nor on-off. We approximate it by an on-off process by defining the process to be off if no fluid of type k is leaving the buffer, and on otherwise. We compute the mean on time τkon and mean off time τkoff. We approximate the peak output rate by a constant rko so as to conserve the fluid. We approximate the output process by the three parameters (λko, μko, rko), where λko = 1/τkoff, and μko = 1/τkon. In this paper we derive methods of computing τkon, τkoff and rko for k = 1, 2,…, K. They are based on the results for the computation of expected reward in a fluid queueing system during a first passage time. We illustrate the methodology by a numerical example. In the last section we conduct a similar output analysis for a standard M/G/1 queue with K types of customers arriving according to independent Poisson processes and requiring independent generally distributed service times, and following a FCFS service discipline. For this case we are able to get analytical results.

For the M/G/c loss system, it is well known that Erlang's loss probability is convex in the number of servers. We extend this result firstly to renewal arrivals and exponential service, then to regenerative arrivals and exponential service, and finally to an arbitrary arrival process with i.i.d. service times that are independent of the arrival process.

We study a service system in which, in each service period, the server performs the current set B of tasks as a batch, taking time s(B), where the function s(·) is subadditive. A natural definition of ‘traffic intensity under congestion’ in this setting is ρ := limt→∞t-1Es (all tasks arriving during time [0,t]). We show that ρ > 1 and a finite mean of individual service times are necessary and sufficient to imply stability of the system. A key observation is that the numbers of arrivals during successive service periods form a Markov chain {An}, enabling us to apply classical regenerative techniques and to express the stationary distribution of the process in terms of the stationary distribution of {An}.

We rigorously prove that for a stochastic process, , the existence of a first regeneration time, R1, implies the existence of an infinite sequence of such times, {R1, R2, · ·· }, and hence that the definition of regenerative process need only demand the existence of a first regeneration time. Here we include very general processes up to and including processes where cycles are stationary but not necessarily independent and identically distributed.

Given a parametric family of regenerative processes on a common probability space, we investigate when the derivatives (with respect to the parameter) are regenerative. We primarily consider sequences satisfying explicit, Lipschitz recursions, such as the waiting times in many queueing systems, and show that derivatives regenerate together with the original sequence under reasonable monotonicity or continuity assumptions. The inputs to our recursions are i.i.d. or, more generally, governed by a Harris-ergodic Markov chain. For i.i.d. input we identify explicit regeneration points; otherwise, we use coupling arguments. We give conditions for the expected steady-state derivative to be the derivative of the steady-state mean of the original sequence. Under these conditions, the derivative of the steady-state mean has a cycle-formula representation.

In this study an asymptotical analysis of the reliability of a complex renewable system with an unbounded number of repair units is provided. The system state is given by a binary vector e(t) = [e1(t), · ··, en(t)], ei(t) = 0(1), if at moment t the ith element is failure-free (failed). We assume that at the state e the ith element has failure intensity λi(e). At the instant of failure of every element the renewal work begins and the renewal time has distribution function Gi(t). Let E_ be the set of failed system states. The goal of this study is the asymptotic estimation of the distribution of the time until the first system failure, .

We consider the stable k-server queue with non-stationary Poisson arrivals and i.i.d. service times and show that the non-time-homogeneous Markov process Zt = (the queue length and residual service times at time t) can be subordinated to a stable time-homogeneous regenerative process. As an application we show that if the system starts from given conditions at time s then the distribution of Zt stabilizes (but depends on t) as s tends backwards to –∞. Also moment and stochastic domination results are established for the delay and recurrence times of the regenerative process leading to results on uniform rates of convergence.

This paper discusses the asymptotic behavior of the Mt/G/c queue having a Poisson arrival process with a general deterministic intensity. Since traditional equilibrium does not always exist, other notions of asymptotic stability are introduced and investigated. For the periodic case, limit theorems are proved complementing Harrison and Lemoine (1977) and Lemoine (1981).