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László A. Székely

Publications and source records attributed to László A. Székely.

15 recordsLinked to original sources
arXiv2023

The largest crossing number of tanglegrams

A tanglegram $\cal T$ consists of two rooted binary trees with the same number of leaves, and a perfect matching between the two leaf sets. In a layout, the tanglegrams is drawn with the leaves on two parallel lines, the trees on either side of the strip created by these lines are drawn as plane trees, and the perfect matching is drawn in straight line segments inside the strip. The tanglegram crossing number ${\rm cr}({\cal T})$ of $\cal T$ is the smallest number of crossings of pairs of matching edges, over all possible layouts of $\cal T$. The size of the tanglegram is the number of matching edges, say $n$. An earlier paper showed that the maximum of the tanglegram crossing number of size $n$ tanglegrams is $<\frac{1}{2}\binom{n}{2}$; but is at least $\frac{1}{2}\binom{n}{2}-\frac{n^{3/2}-n}{2}$ for infinitely many $n$. Now we make better bounds: the maximum crossing number of a size $n$ tanglegram is at most $ \frac{1}{2}\binom{n}{2}-\frac{n}{4}$, but for infinitely many $n$, at least $\frac{1}{2}\binom{n}{2}-\frac{n\log_2 n}{4}$. The problem shows analogy with the Unbalancing Lights Problem of Gale and Berlekamp.

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arXiv2022

Proximity in Triangulations and Quadrangulations

Let $ G $ be a connected graph. If $\barσ(v)$ denotes the arithmetic mean of the distances from $v$ to all other vertices of $G$, then the proximity, $π(G)$, of $G$ is defined as the smallest value of $\barσ(v)$ over all vertices $v$ of $G$. We give upper bounds for the proximity of simple triangulations and quadrangulations of given order and connectivity. We also construct simple triangulations and quadrangulations of given order and connectivity that match the upper bounds asymptotically and are likely optimal.

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arXiv2021

Minimum Wiener Index of Triangulations and Quadrangulations

The Wiener index of a connected graph is the sum of the distances between all unordered pairs of vertices. We provide formulae for the minimum Wiener index of simple triangulations and quadrangulations with connectivity at least $c$, and provide the extremal structures, which attain those values. Our main tool is setting upper bounds for the maximum degree in highly connected triangulations and quadrangulations.

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arXiv2021

Wiener Index and Remoteness in Triangulations and Quadrangulations

Let $G$ be a a connected graph. The Wiener index of a connected graph is the sum of the distances between all unordered pairs of vertices. We provide asymptotic formulae for the maximum Wiener index of simple triangulations and quadrangulations with given connectivity, as the order increases, and make conjectures for the extremal triangulations and quadrangulations based on computational evidence. If $\overlineσ(v)$ denotes the arithmetic mean of the distances from $v$ to all other vertices of $G$, then the remoteness of $G$ is defined as the largest value of $\overlineσ(v)$ over all vertices $v$ of $G$. We give sharp upper bounds on the remoteness of simple triangulations and quadrangulations of given order and connectivity.

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arXiv2020

On the maximum diameter of $k$-colorable graphs

Erdős, Pach, Pollack and Tuza [J. Combin. Theory, B 47, (1989), 279-285] conjectured that the diameter of a $K_{2r}$-free connected graph of order $n$ and minimum degree $δ\geq 2$ is at most $\frac{2(r-1)(3r+2)}{(2r^2-1)}\cdot \frac{n}δ + O(1)$ for every $r\ge 2$, if $δ$ is a multiple of $(r-1)(3r+2)$. For every $r>1$ and $δ\ge 2(r-1)$, we create $K_{2r}$-free graphs with minimum degree $δ$ and diameter $\frac{(6r-5)n}{(2r-1)δ+2r-3}+O(1)$, which are counterexamples to the conjecture for every $r>1$ and $δ>2(r-1)(3r+2)(2r-3)$. The rest of the paper proves positive results under a stronger hypothesis, $k$-colorability, instead of being $K_{k+1}$-free. We show that the diameter of connected $k$-colorable graphs with minimum degree $\geq δ$ and order $n$ is at most $\left(3-\frac{1}{k-1}\right)\frac{n}δ+O(1)$, while for $k=3$, it is at most $\frac{57n}{23δ}+O\left(1\right)$.

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arXiv2020

An infinite antichain of planar tanglegrams

Contrary to the expectation arising from the tanglegram Kuratowski theorem of É. Czabarka, L.A. Székely and S. Wagner [SIAM J. Discrete Math. 31(3): 1732--1750, (2017)], we construct an infinite antichain of planar tanglegrams with respect to the induced subtanglegram partial order. R.E. Tarjan, R. Laver, D.A. Spielman and M. Bóna, and possibly others, showed that the partially ordered set of finite permutations ordered by deletion of entries contains an infinite antichain, i.e. there exists an infinite collection of permutations, such that none of them contains another as a pattern. Our construction adds a twist to the construction of Spielman and Bóna [Electr. J. Comb, Vol. 7. N2.]

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arXiv2018

Inducibility of d-ary trees

Imitating a recently introduced invariant of trees, we initiate the study of the inducibility of $d$-ary trees (rooted trees whose vertex outdegrees are bounded from above by $d\geq 2$) with a given number of leaves. We determine the exact inducibility for stars and binary caterpillars. For $T$ in the family of strictly $d$-ary trees (every vertex has $0$ or $d$ children), we prove that the difference between the maximum density of a $d$-ary tree $D$ in $T$ and the inducibility of $D$ is of order $\mathcal{O}(|T|^{-1/2})$ compared to the general case where it is shown that the difference is $\mathcal{O}(|T|^{-1})$ which, in particular, responds positively to an existing conjecture on the inducibility in binary trees. We also discover that the inducibility of a binary tree in $d$-ary trees is independent of $d$. Furthermore, we establish a general lower bound on the inducibility and also provide a bound for some special trees. Moreover, we find that the maximum inducibility is attained for binary caterpillars for every $d$.

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arXiv2017

Analogies between the crossing number and the tangle crossing number

Tanglegrams are special graphs that consist of a pair of rooted binary trees with the same number of leaves, and a perfect matching between the two leaf-sets. These objects are of use in phylogenetics and are represented with straightline drawings where the leaves of the two plane binary trees are on two parallel lines and only the matching edges can cross. The tangle crossing number of a tanglegram is the minimum crossing number over all such drawings and is related to biologically relevant quantities, such as the number of times a parasite switched hosts. Our main results for tanglegrams which parallel known theorems for crossing numbers are as follows. The removal of a single matching edge in a tanglegram with $n$ leaves decreases the tangle crossing number by at most $n-3$, and this is sharp. Additionally, if $γ(n)$ is the maximum tangle crossing number of a tanglegram with $n$ leaves, we prove $\frac{1}{2}\binom{n}{2}(1-o(1))\leγ(n)<\frac{1}{2}\binom{n}{2}$. Further, we provide an algorithm for computing non-trivial lower bounds on the tangle crossing number in $O(n^4)$ time. This lower bound may be tight, even for tanglegrams with tangle crossing number $Θ(n^2)$.

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arXiv2016

Note on k-planar crossing numbers

The crossing number $cr(G)$ of a graph $G=(V,E)$ is the smallest number of edge crossings over all drawings of $G$ in the plane. For any $k\ge 1$, the $k$-planar crossing number of $G$, $cr_k(G)$, is defined as the minimum of $cr(G_0)+cr(G_1)+\ldots+cr(G_{k-1})$ over all graphs $G_0, G_1,\ldots, G_{k-1}$ with $\cup_{i=0}^{k-1}G_i=G$. It is shown that for every $k\ge 1$, we have $cr_k(G)\le \left(\frac{2}{k^2}-\frac1{k^3}\right)cr(G)$. This bound does not remain true if we replace the constant $\frac{2}{k^2}-\frac1{k^3}$ by any number smaller than $\frac1{k^2}$. Some of the results extend to the rectilinear variants of the $k$-planar crossing number.

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arXiv2016

Paths vs. stars in the local profile of trees

The aim of this paper is to provide an affirmative answer to a recent question by Bubeck and Linial on the local profile of trees. For a tree $T$, let $p^{(k)}_1(T)$ be the proportion of paths among all $k$-vertex subtrees (induced connected subgraphs) of $T$, and let $p^{(k)}_2(T)$ be the proportion of stars. Our main theorem states: if $p^{(k)}_1(T_n) \to 0$ for a sequence of trees $T_1,T_2,\ldots$ whose size tends to infinity, then $p^{(k)}_2(T_n) \to 1$. Both are also shown to be equivalent to the statement that the number of $k$-vertex subtrees grows superlinearly and the statement that the $(k-1)$th degree moment grows superlinearly.

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arXiv2016

Inducibility in binary trees and crossings in random tanglegrams

In analogy to other concepts of a similar nature, we define the inducibility of a rooted binary tree. Given a fixed rooted binary tree $B$ with $k$ leaves, we let $γ(B,T)$ be the proportion of all subsets of $k$ leaves in $T$ that induce a tree isomorphic to $B$. The inducibility of $B$ is $\limsup_{|T| \to \infty} γ(B,T)$. We determine the inducibility in some special cases, show that every binary tree has positive inducibility and prove that caterpillars are the only binary trees with inducibility $1$. We also formulate some open problems and conjectures on the inducibility. Finally, we present an application to crossing numbers of random tanglegrams.

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arXiv2016

On the number of nonisomorphic subtrees of a tree

We show that a tree of order $n$ has at most $O(5^{n/4})$ nonisomorphic subtrees, and that this bound is best possible. We also prove an analogous result for the number of nonisomorphic rooted subtrees of a rooted tree.

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arXiv2015

Abelian groups yield many large families for the diamond problem

There is much recent interest in excluded subposets. Given a fixed poset $P$, how many subsets of $[n]$ can found without a copy of $P$ realized by the subset relation? The hardest and most intensely investigated problem of this kind is when $P$ is a diamond, i.e. the power set of a 2 element set. In this paper, we show infinitely many asymptotically tight constructions using random set families defined from posets based on Abelian groups. They are provided by the convergence of Markov chains on groups. Such constructions suggest that the diamond problem is hard.

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arXiv2012

Mixed orthogonal arrays, $k$-dimensional $M$-part Sperner multi-families, and full multi-transversals

Aydinian et al. [J. Combinatorial Theory A 118(2)(2011), 702-725] substituted the usual BLYM inequality for L-Sperner families with a set of M inequalities for $(m_1,m_2,...,m_M;L_1,L_2,...,L_M)$ type M-part Sperner families and showed that if all inequalities hold with equality, then the family is homogeneous. Aydinian et al. [Australasian J. Comb. 48(2010), 133-141] observed that all inequalities hold with equality if and only if the transversal of the Sperner family corresponds to a simple mixed orthogonal array with constraint M, strength M-1, using $m_i+1$ symbols in the $i^{\text{th}}$ column. In this paper we define $k$-dimensional $M$-part Sperner multi-families with parameters $L_P: P\in\binom{[M]}{k}$ and prove $\binom{M}{k}$ BLYM inequalities for them. We show that if k<M and all inequalities hold with equality, then these multi-families must be homogeneous with profile matrices that are strength M-k mixed orthogonal arrays. For k=M, homogeneity is not always true, but some necessary conditions are given for certain simple families. Following the methods of Aydinian et al. [Australasian J. Comb. 48(2010), 133-141], we give new constructions to simple mixed orthogonal arrays with constraint M, strength M-k, using $m_i+1$ symbols in the ith column. We extend the convex hull method to k-dimensional M-part Sperner multi-families, and allow additional conditions providing new results even for simple 1-part Sperner families.

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