We investigate a trivariate polynomial associated with rooted trees. It generalises a bivariate polynomial for rooted trees that was recently introduced by Liu. We show that this polynomial satisfies a deletion-contraction recursion and can be expressed as a sum over maximal antichains. Several combinatorial quantities can be obtained as special values, in particular the number of antichains, maximal antichains and cutsets. We prove that two of the three possible bivariate specialisations characterise trees uniquely up to isomorphism. One of these has already been established by Liu, the other is new. For the third specialisation, we construct non-isomorphic trees with the same associated polynomial.
We finally find that our polynomial can be generalised in a natural way to a family of posets that we call $\mathcal{V}$-posets. These posets are obtained recursively by either disjoint unions or adding a greatest/least element to existing $\mathcal{V}$-posets.
In this paper we give a generalization of Chebyshev polynomials and using this we describe the Möbius function of the generalized subword order from a poset {a1,...as,c |ai<c}, which contains an affirmative answer for the conjecture by Björner, Sagan, Vatter.[5,10]
Each labeled rooted tree is associated with a hyperplane arrangement, which is free with exponents given by the depths of the vertices of this tree. The intersection lattices of these arrangements are described through posets of forests. These posets are used to define coalgebras, whose dual algebras are shown to have a simple presentation by generators and relations.
HUN-REN Alfréd Rényi Institute of Mathematics（匈牙利科学院阿尔弗雷德·雷尼数学研究所）；Department of Computer Science and Information Theory, Budapest University of Technology and Economics（布达佩斯科技大学计算机科学与信息论系）
We refine a technique used in a paper by Schur on real-rooted polynomials. This amounts to an extension of a theorem of Wagner on Hadamard products of Toeplitz matrices. We also apply our results to polynomials for which the Neggers-Stanley Conjecture is known to hold. More precisely, we settle interlacing properties for $E$-polynomials of series-parallel posets and column-strict labelled Ferrers posets.
Let $T$ be a tree on $n$ vertices with Laplacian $L_T$ and let $GTS_n$ be the generalized tree shift poset on the set of unlabelled trees on $n$ vertices. Inequalities are known for coefficients of the characteristic polynomial of $L_T$ as we go up the poset $GTS_n$. In this work, we generalize these inequalities to the $q$-Laplacian $L^q_T$ of $T$ and to the coefficients of all immanantal polynomials.
The coefficients of the chain polynomial of a finite poset enumerate chains in the poset by their number of elements. The chain polynomials of the partition lattices and their standard type $B$ analogues are shown to have only real roots. The real-rootedness of the chain polynomial is conjectured for all geometric lattices and is shown to be preserved by the pyramid and the prism operations on Cohen--Macaulay posets. As a result, new families of convex polytopes whose face lattices have real-rooted chain polynomials are presented. An application to the face enumeration of the second barycentri…
A rooted tree T is a poset whose Hasse diagram is a graph-theoretic tree having a unique minimal element. We study rowmotion on antichains and lower order ideals of T. Recently Elizalde, Roby, Plante and Sagan considered rowmotion on fences which are posets whose Hasse diagram is a path (but permitting any number of minimal elements). They showed that in this case, the orbits could be described in terms of tilings of a cylinder. They also defined a new notion called homometry which means that a statistic takes a constant value on all orbits of the same size. This is a weaker condition than the…
Let $\T_{n}$ be the set of rooted labeled trees on $\set{0,...,n}$. A maximal decreasing subtree of a rooted labeled tree is defined by the maximal subtree from the root with all edges being decreasing. In this paper, we study a new refinement $\T_{n,k}$ of $\T_n$, which is the set of rooted labeled trees whose maximal decreasing subtree has $k+1$ vertices.
The edge-product space of phylogenetic trees is a regular CW complex whose maximal closed cells correspond to trivalent trees with leaves labeled by a finite set $X$. The face poset of this cell decomposition is isomorphic to the Tuffley poset, a poset of labeled forests, with a unique minimum adjoined. We show that the edge-product space of phylogenetic trees is gallery-connected. We then use combinatorial properties of the Tuffley poset and a related graph known as NNI-tree space to show that, although open intervals of the Tuffley poset were proven to be shellable by Gill, Linusson, Moulton…
We give exact formulas for the transmission (i.e. the sum of all distances between vertices) of perfect trees and rooted powers of (connected finite) graphs.
Let $T$ be a tree on $n$ vertices with $q$-Laplacian $L_{T}^{q}$. Let $GTS_n$ be the generalized tree shift poset on the set of unlabelled trees with $n$ vertices. We prove that for all $q \in R$, going up on $GTS_n$ has the following effect: the spectral radius and the second smallest eigenvalue of $L_{T}^{q}$ increase while the smallest eigenvalue of $L_{T}^{q}$ decreases. These generalize known results for eigenvalues of the Laplacian. As a corollary, we obtain consequences about the eigenvalues of $q,t$-Laplacians and exponential distance matrices of trees.
The N cardinality k ideals of any w-element poset (w, k variable) can be enumerated in time O(Nw^3). The corresponding bound for k-element subtrees of a w-element tree is O(Nw^5). An algorithm is described that by the use of wildcards displays all order ideals of a poset in a compact manner, i.e. not one by one.
Bonato and Tardif conjectured that the number of isomorphism classes of trees mutually embeddable with a given tree T is either 1 or infinite. We prove the analogue of their conjecture for rooted trees. We also discuss the original conjecture for locally finite trees and state some new conjectures.
In the work [4] tree-rooted planar cubic maps with marked directed edge (not in this tree) were enumerated. The number of such objects with $2n$ vertices is $C_{2n}\cdot C_{n+1}$, where $C_k$ is Catalan number. In this work a marked directed edge is not demanded, i.e. we enumerate tree-rooted planar cubic maps. Formulas are more complex, of course, but not significantly.
We obtain a differential equation for the enumeration of the path length of general increasing trees. By using differential operators and their combinatorial interpretation we give a bijective proof of a version of Faà di Bruno formula, and model the generation of ballot and Dyck paths. We get formulas for its enumeration according with the height of their lattice points. Recursive formulas for the enumeration of enriched increasing trees and forests with respect to the height of their internal and external vertices are also obtained. Finally we present a generalized form of all those results …
We consider two varieties of labeled rooted trees, and the probability that a vertex chosen from all vertices of all trees of a given size uniformly at random has a given rank. We prove that this probability converges to a limit as the tree size goes to infinity.
In a rooted tree, we call a vertex {\em balanced} if it is at equal distance from all its descendant leaves. We count balanced vertices in three different tree varieties. For decreasing binary trees, we can prove that the probability that a vertex chosen uniformly at random from the set of all trees of a given size is balanced is monotone decreasing.
The perturbation expansion of the solution of a fixed point equation or of an ordinary differential equation may be expressed as a power series in the perturbation parameter. The terms in this series are indexed by rooted trees and depend on a parameter in the equation in a way determined by the structure of the tree. Power series of this form may be considered more generally; there are two interesting and useful group structures on these series, corresponding to operations of composition and substitution. The composition operation defines the Butcher group, an infinite dimensional group that …
We find a simple, closed formula for the proportion of vertices which are $k$-protected in all unlabeled rooted plane trees on $n$ vertices. We also find that, as $n$ goes to infinity, the average rank of a random vertex in a tree of size $n$ approaches 0.727649, and the average rank of the root of a tree of size $n$ approaches 1.62297.
In this article, we construct explicit examples of pairs of non-isomorphic trees with the same restricted $U$-polynomial for every $k$; by this we mean that the polynomials agree on terms with degree at most $k+1$. The main tool for this construction is a generalization of the $U$-polynomial to rooted graphs, which we introduce and study in this article. Most notably we show that rooted trees can be reconstructed from its rooted $U$-polynomial.
Determining whether two graphs are isomorphic is an important and difficult problem in graph theory. One way to make progress towards this problem is by finding and studying graph invariants that distinguish large classes of graphs. Stanley conjectured that his chromatic symmetric function distinguishes all trees, which has remained unresolved. Recently, Hasebe and Tsujie introduced an analogue of Stanley's function for posets, called the strict order quasisymmetric function, and proved that it distinguishes all rooted trees. In this paper, we devise a procedure to explicitly reconstruct a roo…
The number of tree-rooted maps, that is, rooted planar maps with a distinguished spanning tree, of size $n$ is C(n)C(n+1) where C(n)=binomial(2n,n)/(n+1) is the nth Catalan number. We present a (long awaited) simple bijection which explains this result. We prove that our bijection is isomorphic to a former recursive construction on shuffles of parenthesis systems due to Cori, Dulucq and Viennot.
Seo and Shin showed that the number of rooted trees on $[n+1]$ such that the maximal decreasing subtree with the same root has $k+1$ vertices is equal to the number of functions $f:[n]\to[n]$ such that the image of $f$ contains $[k]$. We give a bijective proof of this theorem.
We study the bounded regions in a generic slice of the hyperplane arrangement in $\mathbb{R}^n$ consisting of the hyperplanes defined by $x_i$ and $x_i+x_j$. The bounded regions are in bijection with several classes of combinatorial objects, including the ordered partitions of $[n]$ all of whose left-to-right minima occur at odd locations and the drawings of rooted plane trees with $n+1$ vertices. These are sequences of rooted plane trees such that each tree in a sequence can be obtained from the next one by removing a leaf.
In this paper, we give a decomposition of triply rooted trees into three doubly rooted trees. This leads to a combinatorial interpretation of an identity conjectured by Lacasse in the study of the PAC-Bayesian machine learning theory, and proved by Younsi by using the Hurwitz identity on multivariate Abel polynomials. We also give a bijection between the set of functions from $[n+1]$ to $[n]$ and the set of triply rooted trees on $[n]$, which leads to the refined enumeration of functions from $[n+1]$ to $[n]$ with respect to the number of elements in the orbit of $n+1$ and the number of period…
We consider planar cubic maps, i.e. connected cubic graphs imbedded into plane, with marked spanning tree and marked directed edge (not in this tree). The number of such objects with $2n$ vertices is $C_{2n}\cdot C_{n+1}$, where $C_k$ is $k$-th Catalan number.
In this paper we enumerate the cardinalities for the set of all vertices of outdegree $\ge k$ at level $\ge \ell$ among all rooted ordered $d$-trees with $n$ edges. Our results unite and generalize several previous works in the literature.
Rooted triples, rooted binary phylogenetic trees on three leaves, are sufficient to encode rooted binary phylogenetic trees. That is, if $\mathcal T$ and $\mathcal T'$ are rooted binary phylogenetic $X$-trees that infers the same set of rooted triples, then $\mathcal T$ and $\mathcal T'$ are isomorphic. However, in general, this sufficiency does not extend to rooted binary phylogenetic networks. In this paper, we show that trinets, phylogenetic network analogues of rooted triples, are sufficient to encode rooted binary orchard networks. Rooted binary orchard networks naturally generalise roote…
Binary rooted trees, both in the ordered and in the un-ordered case, are well studied structures in the field of combinatorics. The aim of this work is to study particular patterns in these classes of trees. We consider completely unbalanced subtrees, where unbalancing is measured according to the so-called Colless's index. The size of the biggest unbalanced subtree becomes then a new parameter with respect to which we find several enumerations.
The independence polynomial of a graph $G$ is \[I(G,x)=\sum\limits_{k\ge 0}i_k(G)x^k,\] where $i_k(G)$ denotes the number of independent sets of $G$ of size $k$ (note that $i_0(G)=1$). In this paper we show a new method to prove real-rootedness of the independence polynomials of certain families of trees. In particular we will give a new proof of the real-rootedness of the independence polynomials of centipedes (Zhu's theorem), caterpillars (Wang and Zhu's theorem), and we will prove a conjecture of Galvin and Hilyard about the real-rootedness of the independence polynomial of the so-called Fi…
Richard P. Stanley conjectured that finite trees can be distinguished by their chromatic symmetric functions. In this paper, we prove an analogous statement for posets: Finite rooted trees can be distinguished by their order quasisymmetric functions.
Trees or rooted trees have been generously studied in the literature. A forest is a set of trees or rooted trees. Here we give recurrence relations between the number of some kind of rooted forest with $k$ roots and that with $k+1$ roots on $\{1,2,\ldots,n\}$. Classical formulas for counting various trees such as rooted trees, bipartite trees, tripartite trees, plane trees, $k$-ary plane trees, $k$-edge colored trees follow immediately from our recursive relations.
Let $\mathcal{T}_n$ be the set of trees with $n$ vertices. Suppose that each tree in $\mathcal{T}_n$ is equally likely. We show that the number of different rooted trees of a tree equals $(μ_r+o(1))n$ for almost every tree of $\mathcal{T}_n$, where $μ_r$ is a constant. As an application, we show that the number of any given pattern in $\mathcal{T}_n$ is also asymptotically normally distributed with mean $\sim μ_M n$ and variance $\sim σ_M n$, where $μ_M, σ_M$ are some constants related to the given pattern. This solves an open question claimed in Kok's thesis.
The incidence category $\C_{\F}$ of a family $\F$ of colored posets closed under disjoint unions and the operation of taking convex sub-posets was introduced by the author in \cite{Sz}, where the Ringel-Hall algebra $\H_{\F}$ of $\C_{\F}$ was also defined. We show that if the Hasse diagrams underlying $\F$ are rooted trees, then the subspace $\n_{\F}$ of primitive elements of $\H_{\F}$ carries a pre-Lie structure, defined over $\mathbb{Z}$, and with positive structure constants. We give several examples of $\n_{\F}$, including the nilpotent subalgebras of $\mathfrak{sl}_n$, $L \mathfrak{gl}_n$…
The interior and exterior activities of bases of a matroid are well-known notions that for instance permit one to define the Tutte polynomial. Recently, we have discovered correspondences between the regions of gainic hyperplane arrangements and coloredlabeled rooted trees. Here we define a general activity theory that applies in particular to no-broken circuit (NBC) sets and labeled colored trees. The special case of activity \textsf{0} was our motivating case. As a consequence, in a gainic hyperplane arrangement the number of bounded regions is equal to the number of the corresponding colore…
Two decades ago, Chauve, Dulucq and Guibert showed that the number of rooted trees on the vertex set $[n+1]$ in which exactly $k$ children of the root are lower-numbered than the root is $\binom{n}{k} \, n^{n-k}$. Here I give a simpler proof of this result.
