Related papers: Euler-genus distributions of cubic Halin graphs

Traditional representations of graphs and their duals suggest the requirement that the dual vertices be placed inside their corresponding primal faces, and the edges of the dual graph cross only their corresponding primal edges. We consider…

This paper introduces a new systematic algorithm for constructing periodic Euclidean weaving diagrams with combinatorial arguments. It is shown that such a weaving diagram can be considered as a specific type of four-regular periodic planar…

We present an extensive study of the Eulerian distribution on the set of self evacuated involutions, namely, involutions corresponding to standard Young tableaux that are fixed under the Sch$\ddot{\textrm{u}}$tzenberger map. We find some…

We equip the space of lattice cones with a coproduct which makes it a connected cograded colagebra. The exponential sum and exponential integral on lattice cones can be viewed as linear maps on this space with values in the space of…

We show that the number of $k$-matching in a given undirected graph $G$ is equal to the number of perfect matching of the corresponding graph $G_k$ on an even number of vertices divided by a suitable factor. If $G$ is bipartite then one can…

Genus 2 curves have been an object of much mathematical interest since eighteenth century and continued interest to date. They have become an important tool in many algorithms in cryptographic applications, such as factoring large numbers,…

We show how to construct an explicit Hamilton cycle in the directed Cayley graph Cay({\sigma_n, sigma_{n-1}} : \mathbb{S}_n), where \sigma_k = (1 2 >... k). The existence of such cycles was shown by Jackson (Discrete Mathematics, 149 (1996)…

We apply classical invariant theory of binary forms to explicitly characterize isomorphism classes of hyperelliptic curves of small genus and, conversely, propose algorithms for reconstructing hyperelliptic models from given invariants. We…

Consider a pair of plane straight-line graphs, whose edges are colored red and blue, respectively, and let n be the total complexity of both graphs. We present a O(n log n)-time O(n)-space technique to preprocess such pair of graphs, that…

We propose an effective algorithm that enumerates (and actually finds) all 3-edge colorings and Hamiltonian cycles in a cubic graph. The idea is to make a preliminary run that separates the vertices into two types: ``rigid'' (such that the…

A 2-matching of a graph $G$ is a spanning subgraph with maximum degree two. The size of a 2-matching $U$ is the number of edges in $U$ and this is at least $n-\k(U)$ where $n$ is the number of vertices of $G$ and $\k$ denotes the number of…

If the cyclic sequence of faces for all the vertices in a map are of same type, then the map is said to be a semi-equivelar map. In this article, we classify all the types of semi-equivelar maps on the surface of Euler genus 3, $i.e.$, on…

We show that linearly repetitive weighted Delone sets in groups of polynomial growth have a uniquely ergodic hull. This result applies in particular to the linearly repetitive weighted Delone sets in homogeneous Lie groups constructed in…

A graph $G$ is said to be Hamiltonian if it contains a spanning cycle. In this work, we investigate the Hamiltonian completeness of certain classes of caterpillar graphs, which are trees with a central path to which all other vertices are…

It is a well-known fact that genetic sequences may contain sections with repeated units, called repeats, that differ in length over a population, with a length distribution of geometric type. A simple class of recombination models with…

We study the statistics of Hamiltonian cycles on various families of bicolored random planar maps (with the spherical topology). These families fall into two groups corresponding to two distinct universality classes with respective central…

We propose a partitioning of the set of unlabelled, connected cubic graphs into two disjoint subsets named genes and descendants, where the cardinality of the descendants is much larger than that of the genes. The key distinction between…

We introduce a new array of type $D$ Eulerian numbers, different from that studied by Brenti, Chow and Hyatt. We find in particular the recurrence relation, Worpitzky formula and the generating function. We also find the probability…

In this paper we compute the bivariate generating function of $\gamma$-matchings over two backbones, filtered by the number of arcs and the topological genus. $\gamma$-matchings over two backbones are chord-diagrams, obtained via…

The study of partial-twuality polynomials originates from the classical operations of geometric duality and Petrie duality on cellularly embedded graphs. These involutions generate the symmetric group $S_3$, and applying them to subsets of…