In the full rectangular version of Gilbert's planar tessellation (see Gilbert (1967), Mackisack and Miles (1996), and Burridge et al. (2013)), lines extend either horizontally (with east- and west-growing rays) or vertically (north- and south-growing rays) from seed points which form a stationary Poisson point process, each ray stopping when it meets another ray that has blocked its path. In the half-Gilbert rectangular version, east- and south-growing rays, whilst having the potential to block each other, do not interact with west and north rays, and vice versa. East- and south-growing rays have a reciprocality of blocking, as do west and north. In this paper we significantly expand and simplify the half-Gilbert analytic results that we gave in Burridge et al. (2013). We also show how the idea of reciprocality of blocking between rays can be used in a much wider context, with rays not necessarily orthogonal and with seeds that produce more than two rays.

We investigate the ray-length distributions for two different rectangular versions of Gilbert's tessellation (see Gilbert (1967)). In the full rectangular version, lines extend either horizontally (east- and west-growing rays) or vertically (north- and south-growing rays) from seed points which form a Poisson point process, each ray stopping when another ray is met. In the half rectangular version, east- and south-growing rays do not interact with west and north rays. For the half rectangular tessellation, we compute analytically, via recursion, a series expansion for the ray-length distribution, whilst, for the full rectangular version, we develop an accurate simulation technique, based in part on the stopping-set theory for Poisson processes (see Zuyev (1999)), to accomplish the same. We demonstrate the remarkable fact that plots of the two distributions appear to be identical when the intensity of seeds in the half model is twice that in the full model. In this paper we explore this coincidence, mindful of the fact that, for one model, our results are from a simulation (with inherent sampling error). We go on to develop further analytic theory for the half-Gilbert model using stopping-set ideas once again, with some novel features. Using our theory, we obtain exact expressions for the first and second moments of the ray length in the half-Gilbert model. For all practical purposes, these results can be applied to the full-Gilbert model—as much better approximations than those provided by Mackisack and Miles (1996).

The iterative division of a triangle by chords which join a randomly-selected vertex of a triangle to the opposite side is investigated. Results on the limiting random graph which eventuates are given. Aspects studied are: the order of vertices; the fragmentation of chords; age distributions for elements of the graph; various topological characterisations of the triangles. Different sampling protocols are explored. Extensive use is made of the theory of branching processes.

It is shown here that, for $n\ge 2$, the $n$-torus is the only $n$-dimensional compact euclidean space-form which can admit a regular or chiral tessellation. Further, such a tessellation can only be chiral if $n\,=\,2$.