We consider Gaussian approximation in a variant of the classical Johnson–Mehl birth–growth model with random growth speed. Seeds appear randomly in $\mathbb{R}^d$ at random times and start growing instantaneously in all directions with a random speed. The locations, birth times, and growth speeds of the seeds are given by a Poisson process. Under suitable conditions on the random growth speed, the time distribution, and a weight function $h\;:\;\mathbb{R}^d \times [0,\infty) \to [0,\infty)$, we prove a Gaussian convergence of the sum of the weights at the exposed points, which are those seeds in the model that are not covered at the time of their birth. Such models have previously been considered, albeit with fixed growth speed. Moreover, using recent results on stabilization regions, we provide non-asymptotic bounds on the distance between the normalized sum of weights and a standard Gaussian random variable in the Wasserstein and Kolmogorov metrics.

In this paper we introduce multitype branching processes with inhomogeneous Poisson immigration, and consider in detail the critical Markov case when the local intensity r(t) of the Poisson random measure is a regularly varying function. Various multitype limit distributions (conditional and unconditional) are obtained depending on the rate at which r(t) changes with time. The asymptotic behaviour of the first and second moments, and the probability of nonextinction are investigated.

We define a class of tessellation models based on perturbing or deforming standard tessellations such as the Voronoi tessellation. We show how distributions over this class of ‘deformed’ tessellations can be used to define prior distributions for models based on tessellations, and how inference for such models can be carried out using Markov chain Monte Carlo methods; stability properties of the algorithms are investigated. Our approach applies not only to fixed dimension problems, but also to variable dimension problems, in which the number of cells in the tessellation is unknown. We illustrate our methods with two real examples. The first relates to reconstructing animal territories, represented by the individual cells of a tessellation, from observation of an inhomogeneous Poisson point process. The second example involves the analysis of an image of a cross-section through a sample of metal, with the tessellation modelling the micro-crystalline structure of the metal.

Consider an inhomogeneous Poisson process X on [0, T] whose unknown intensity function ‘switches' from a lower function g∗ to an upper function h∗ at some unknown point θ∗. What is known are continuous bounding functions g and h such that g∗(t) ≤ g(t) ≤ h(t) ≤ h∗(t) for 0 ≤ t ≤ T. It is shown that on the basis of n observations of the process X the maximum likelihood estimate of θ∗ is consistent for n →∞, and also that converges in law and in pth moment to limits described in terms of the unknown functions g∗ and h∗.

Consider the following birth-growth model in ℝ. Seeds are born randomly according to an inhomogeneous space-time Poisson process. A newly formed point immediately initiates a bi-directional coverage by sending out a growing branch. Each frontier of a branch moves at a constant speed until it meets an opposing one. New seeds continue to form on the uncovered parts on the line. We are interested in the time until a bounded interval is completely covered. The exact and limiting distributions as the length of interval tends to infinity are obtained for this completion time by considering a related Markov process. Moreover, some strong limit results are also established.