Related papers: Height restricted lattice paths, Elenas, and bijec…
In this paper we establish six bijections between a particular class of polyominoes, called deco polyominoes, enumerated according to their directed height by n!, and permutations. Each of these bijections allows us to establish different…
We unify and extend previous bijections on plane quadrangulations to bipartite and quasibipartite plane maps. Starting from a bipartite plane map with a distinguished edge and two distinguished corners (in the same face or in two different…
There are several combinatorial objects that are known to be in bijection to the spanning trees of a graph G. These objects include G-parking functions, critical configurations of G, and descending traversals of G. In this paper, we extend…
In this article we investigate the lattices of Dyck paths of type $A$ and $B$ under dominance order, and explicitly describe their Heyting algebra structure. This means that each Dyck path of either type has a relative pseudocomplement with…
Rotation distances measure the differences in structure between rooted ordered binary trees. The one-dimensional skeleta of associahedra are rotation graphs, where two vertices representing trees are connected by an edge if they differ by a…
The enumeration of maps and the study of uniform random maps have been classical topics of combinatorics and statistical physics ever since the seminal work of Tutte in the sixties. Following the bijective approach initiated by Cori and…
Multi-edge trees as introduced in a recent paper of Dziemia\'nczuk are plane trees where multiple edges are allowed. We first show that $d$-ary multi-edge trees where the out-degrees are bounded by $d$ are in bijection with classical…
We characterize all residuated lattices that have height equal to $3$ and show that the variety they generate has continuum-many subvarieties. More generally, we study unilinear residuated lattices: their lattice is a union of disjoint…
It has recently been shown that any simple (i.e. nonintersecting) polygonal chain in the plane can be reconfigured to lie on a straight line, and any simple polygon can be reconfigured to be convex. This result cannot be extended to tree…
A lattice $\Lambda$ is said to be an extension of a sublattice $L$ of smaller rank if $L$ is equal to the intersection of $\Lambda$ with the subspace spanned by $L$. The goal of this paper is to initiate a systematic study of the geometry…
A flip in a plane spanning tree $T$ is the operation of removing one edge from $T$ and adding another edge such that the resulting structure is again a plane spanning tree. For trees on a set of points in convex position we study two…
The rank (also known as protection number or leaf-height) of a vertex in a rooted tree is the minimum distance between the vertex and any of its leaf descendants. We consider the sum of ranks over all vertices (known as the security) in…
It is well-known that plane partitions, lozenge tilings of a hexagon, perfect matchings on a honeycomb graph, and families of non-intersecting lattice paths in a hexagon are all in bijection. In this work we consider regions that are more…
We consider posets of lattice paths (endowed with a natural order) and begin the study of such structures. We give an algebraic condition to recognize which ones of these posets are lattices. Next we study the class of Dyck lattices (i.e.,…
We consider maps on orientable surfaces. A map is called \emph{unicellular} if it has a single face. A \emph{covered map} is a map (of genus $g$) with a marked unicellular spanning submap (which can have any genus in $\{0,1,...,g\}$). Our…
Assume that we embed the path $P_n$ as a subgraph of a $2$-dimensional grid, namely, $P_k \times P_l$. Given such an embedding, we consider the ordered set of subpaths $L_1, L_2, \ldots , L_m$ which are maximal straight segments in the…
Matchings are frequently used to model RNA secondary structures; however, not all matchings can be realized as RNA motifs. One class of matchings, called the L $\&$ P matchings, is the most restrictive model for RNA secondary structures in…
We show how a bijection due to Biane between involutions and labelled Motzkin paths yields bijections between Motzkin paths and two families of restricted involutions that are counted by Motzkin numbers, namely, involutions avoiding 4321…
We define a minimization problem for paths on planar graphs that, on the honeycomb lattice, is equivalent to the exploration path of the critical site percolation and than has the same scaling limit of SLE_6. We numerically study this model…
We present a simple bijection between permutation matrices and descending plane partitions without special parts. This bijection is already mentioned in work of P. Lalonde (without giving the details); it involves the inversion words of…