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.

We study a parametric class of isotropic but not necessarily stationary Poisson hyperplane tessellations in n-dimensional Euclidean space. Our focus is on the volume of the zero cell, i.e. the cell containing the origin. As a main result, we obtain an explicit formula for the variance of the volume of the zero cell in arbitrary dimensions. From this formula we deduce the asymptotic behaviour of the volume of the zero cell as the dimension goes to ∞.

For stationary Poisson hyperplane tessellations in d-dimensional Euclidean space and a dimension k ∈ {1, …, d}, we investigate the typical k-face and the weighted typical k-face (weighted by k-dimensional volume), without isotropy assumptions on the tessellation. The case k = d concerns the previously studied typical cell and zero cell, respectively. For k < d, we first find the conditional distribution of the typical k-face or weighted typical k-face, given its direction. Then we investigate how the shapes of the faces are influenced by assumptions of different types: either via containment of convex bodies of given volume (including a new result for k = d), or, for weighted typical k-faces, in the spirit of D. G. Kendall's asymptotic problem, suitably generalized. In all these results on typical or weighted typical k-faces with given direction space L, the Blaschke body of the section process of the underlying hyperplane process with L plays a crucial role.

We consider a stationary Poisson process X of k-flats in ℝd with intensity measure Θ and a measurable set S of k-flats depending on F1,…,Fn∈ X, x∈ℝd, and X in a specific equivariant way. If (F1,…,Fn,x) is properly sampled (in a ‘typical way’) then Θ(S) has a gamma distribution. This result generalizes and unifies earlier work by Miles (1971), Møller and Zuyev (1996), and Zuyev (1999). As a new example, we will show that the volume of the fundamental region of a typical j-face of a stationary Poisson–Voronoi tessellation is conditionally gamma distributed. This is true in the area-biased and the area-debiased cases. In the first case the shape parameter is not integer valued. As another new example, we will show that the generalized integral-geometric contents of the (area-biased and area-debiased) typical j-face of a Poisson hyperplane tessellation are conditionally gamma distributed. In the isotropic case the contents boil down to the mean breadth of the face.

We study lower-dimensional volume-weighted typical faces of a stationary Poisson hyperplane tessellation in d-dimensional Euclidean space. After showing how their distribution can be derived from that of the zero cell, we obtain sharp lower and upper bounds for the expected vertex number of the volume-weighted typical k-face (k=2,…,d). The bounds are respectively attained by parallel mosaics and by isotropic tessellations. We conclude with a remark on expected face numbers and expected intrinsic volumes of the zero cell.

It is proved that the shape of the typical cell of a stationary Poisson-Voronoi tessellation in Euclidean space, under the condition that the volume of the typical cell is large, must be close to spherical, with high probability. The same holds if the volume is replaced by the surface area or other suitable functionals. Similar results are established for the zero cell of a stationary and isotropic Poisson hyperplane tessellation.