Groups acting on horocyclic products
Noah Caplinger, Daniel N. Levitin
TL;DR
The paper analyzes finitely generated groups acting geometrically on horocyclic products $X\bowtie Y$ of proper, geodesically complete $\mathop{CAT}(-\kappa)$ spaces, showing a boundary-driven trichotomy: either the group is not finitely presented (if both boundary components are disconnected), an ascending HNN extension of a finitely generated virtually nilpotent group (if exactly one boundary component is connected), or a finite-index subgroup that is a semidirect product of a virtually nilpotent group with $\mathbb{Z}$ (if both boundaries are connected). The authors develop a new metric $d'_X$ on $X$ and analyze the isometry group of horocyclic products by decomposing actions into factorwise components on $X'$ and $Y'$, proving a near-product structure up to a $\mathbb{Z}/2\mathbb{Z}$ swap. A key technique is upgrading arbitrary geometric actions to actions on millefeuille spaces $Z\bowtie W$ via Caprace–Cornulier–Monod–Tessera, enabling a boundary-to-algebra correspondence that detects Heintze versus nilpotent factors and yields strong structural conclusions about the acting groups. The results unify and extend known examples (lamplighter, BS(1,n), and $\mathbb{Z}^2\rtimes_A\mathbb{Z}$ actions) and provide a pathway toward quasi-isometric rigidity insights for horocyclic products. The work leverages Ferragut’s visual-boundary framework and CCMT’s Millefeuille theory to connect geometric properties of boundaries with exact algebraic decompositions.
Abstract
Horocyclic products are a well-studied class of metric spaces that provide models for various solvable Lie groups, Baumslag-Solitar groups, and Lamplighter groups. Let $G$ act geometrically on a horocyclic product $X \bowtie Y$ of $\CAT(-κ)$ spaces $X,Y$. We show that every such group is either an ascending HNN extension of a finitely-generated virtually nilpotent group, or else is not finitely presented, depending on the connectivity of the visual boundary of $X\bowtie Y$.
