Related papers: Distances on the tropical line determined by two p…

We study tropical line arrangements associated to a three-regular graph $G$ that we refer to as \emph{tropical graph curves}. Roughly speaking, the tropical graph curve associated to $G$, whose genus is $g$, is an arrangement of $2g-2$…

A long-standing conjecture on spanning trees of a hypercube states that a balanced tree on $2^n$ vertices with maximum degree at most $3$ spans the hypercube of dimension $n$ \cite{havel1986}. In this paper, we settle the conjecture for a…

We introduce the notion of tropical area of a tropical curve defined in an open subset of $\mathbb R^n$. We prove that the number of vertices of a tropical curve is bounded by the area of the curve. The approach is totally elementary yet…

We consider special cases of the two tree degree sequences problem. We show that if two tree degree sequences do not have common leaves then they always have edge-disjoint caterpillar realizations. By using a probabilistic method, we prove…

In this paper, we consider the edge disjoint caterpillar realizations of tree degree sequences. We give the necessary and sufficient conditions when two tree degree sequences have edge disjoint caterpillar realizations. We conjecture that…

The problem of comparing trees representing the evolutionary histories of cancerous tumors has turned out to be crucial, since there is a variety of different methods which typically infer multiple possible trees. A departure from the…

For a given metric space $(P,\phi)$, a tree cover of stretch $t$ is a collection of trees on $P$ such that edges $(x,y)$ of trees receive length $\phi(x,y)$, and such that for any pair of points $u,v\in P$ there is a tree $T$ in the…

We study the problem of how well a tree metric is able to preserve the sum of pairwise distances of an arbitrary metric. This problem is closely related to low-stretch metric embeddings and is interesting by its own flavor from the line of…

We consider the number of distinct distances between two finite sets of points in ${\bf R}^k$, for any constant dimension $k\ge 2$, where one set $P_1$ consists of $n$ points on a line $l$, and the other set $P_2$ consists of $m$ arbitrary…

A graph G=(V,E) with m edges is graceful if it has a distinct vertex labeling f, a map from V into the set{0,1,2,3,...,m} which induces a distinct edge labeling |f(u)-f(v)| for edges uv in E. The famous Ringel-Kotzig conjecture (1964) is…

For a vertex $v$ of a graph $G$, a spanning tree $T$ of $G$ is distance-preserving from $v$ if, for any vertex $w$, the distance from $v$ to $w$ on $T$ is the same as the distance from $v$ to $w$ on $G$. If two vertices $u$ and $v$ are…

Given a set of points $P \subset \mathbb F_q^2$ such that $|P|\geq q^{3/2}$ it is established that $|P|$ determines $\Omega(q^2)$ distinct perpendicular bisectors. It is also proven that, if $|P| \geq q^{4/3}$, then for a positive…

The main goal of this paper is to establish the higher-dimensional Nevanlinna theory in tropical geometry. We first develop a theory of tropical meromorphic functions ( holomorphic maps) in several variables, such as the proximity function,…

A Laman graph $G$ is a minimally rigid graph in dimension two, and its realization number is its number of distinct embeddings with fixed generic edge lengths. While conjectured to grow exponentially in the number of vertices of $G$, the…

In this paper, we study tropicalisations of families of curves with a singularity in a fixed point. The tropicalisation of such a family is a linear tropical variety. We describe its maximal dimensional cones using results about linear…

A rooted tree $T$ with vertex labels $t(v)$ and set-valued edge labels $\lambda(e)$ defines maps $\delta$ and $\varepsilon$ on the pairs of leaves of $T$ by setting $\delta(x,y)=q$ if the last common ancestor $\text{lca}(x,y)$ of $x$ and…

We launch the study of the tropicalization of the symplectic Grassmannian, that is, the space of all linear subspaces that are isotropic with respect to a fixed symplectic form. We formulate tropical analogues of several equivalent…

Let $T$ be a tree with $n$ vertices. To each edge of $T$, we assign a weight which is a positive definite matrix of some fixed order, say, $s$. Let $D_{ij}$ denote the sum of all the weights lying in the path connecting the vertices $i$ and…

We present a version of the tropical Nevanlinna theory for real-valued, continuous, piecewise linear functions on the real line. In particular, a tropical version of the second main theorem is proved. Applications to some ultra-discrete…

Maximum parsimony distance is a measure used to quantify the dissimilarity of two unrooted phylogenetic trees. It is NP-hard to compute, and very few positive algorithmic results are known due to its complex combinatorial structure. Here we…