Tree-chromatic number is a chromatic version of treewidth, where the cost of a bag in a tree-decomposition is measured by its chromatic number rather than its size. Path-chromatic number is defined analogously. These parameters were introduced by Seymour (JCTB 2016). In this paper, we survey all the known results on tree- and path-chromatic number and then present some new results and conjectures. In particular, we propose a version of Hadwiger's Conjecture for tree-chromatic number. As evidence that our conjecture may be more tractable than Hadwiger's Conjecture, we give a short proof that every $K_5$-minor-free graph has tree-chromatic number at most $4$, which avoids the Four Colour Theorem. We also present some hardness results and conjectures for computing tree- and path-chromatic number.
In this paper we prove that the dominator chromatic number of every oriented tree is invariant under reversal of orientation. In addition to this marquee result, we also prove the exact dominator chromatic number for arborescences and anti-arborescences as well as bounds on other orientations of oft studied tree topologies including generalized stars and caterpillars.
In a recent article [5], the authors claim that the distance between the b-chromatic index of a tree and a known upper bound is at most 1. At the same time, in [7] the authors claim to be able to construct a tree where this difference is bigger than 1. However, the given example was disconnected, i.e., actually consisted of a forest. Here, we slightly modify their construction in order to produce trees, thus getting that indeed the difference between the b-chromatic index of trees and the known upper bound can be arbitrarily large. We also point out the mistake made in [5].
A heterochromatic (or rainbow) graph is an edge-colored graph whose edges have distinct colors, that is, where each color appears at most once. In this paper, I propose a $(g,f)$-chromatic graph as an edge-colored graph where each color $c$ appears at least $g(c)$ times and at most $f(c)$ times. I also present a necessary and sufficient condition for edge-colored graphs (not necessary to be proper) to have a $(g,f)$-chromatic spanning tree. Using this criterion, I show that an edge-colored complete graph $G$ has a spanning tree with a color probability distribution `similar' to that of $G$. Mo…
We apply Ramsey theoretic tools to show that there is a family of graphs which have tree-chromatic number at most~$2$ while the path-chromatic number is unbounded. This resolves a problem posed by Seymour.
For a graph $G$ and a tree-decomposition $(T, \mathcal{B})$ of $G$, the chromatic number of $(T, \mathcal{B})$ is the maximum of $χ(G[B])$, taken over all bags $B \in \mathcal{B}$. The tree-chromatic number of $G$ is the minimum chromatic number of all tree-decompositions $(T, \mathcal{B})$ of $G$. The path-chromatic number of $G$ is defined analogously. In this paper, we introduce an operation that always increases the path-chromatic number of a graph. As an easy corollary of our construction, we obtain an infinite family of graphs whose path-chromatic number and tree-chromatic number are dif…
Let $G$ be a simple finite connected graph of order $n$. The detour distance between two distinct vertices $u$ and $v$ denoted by $D(u,v)$ is the length of a longest $uv$-path in $G$. A hamiltonian coloring $h$ of a graph $G$ of order $n$ is a mapping $h : V(G) \rightarrow \{0,1,2,...\}$ such that $D(u,v) + |h(u)-h(v)| \geq n-1$, for every two distinct vertices $u$ and $v$ of $G$. The span of $h$, denoted by $span(h)$, is $\max\{|h(u)-h(v)| : u, v \in V(G)\}$. The hamiltonian chromatic number of $G$ is defined as $hc(G) := \min\{span(h)\}$ with minimum taken over all hamiltonian coloring $h$ o…
Erdős proved that there are graphs with arbitrarily large girth and chromatic number. We study the extension of this for generalized chromatic numbers.
In this note we show every orientation of a connected cubic graph admits an oriented 8-colouring. This lowers the best-known upper bound for the chromatic number of the family of orientations of connected cubic graphs. We further show that every such oriented graph admits a 2-dipath 7-colouring. These results imply that either the chromatic number for the family of oriented connected cubic graphs equals the 2-dipath chromatic number or the long-standing conjecture of Sopena [Journal of Graph Theory 25:191-205 1997] regarding the chromatic number of orientations of connected cubic graphs is fal…
We show that no tree on twenty vertices with maximum degree ten has Schur positive chromatic symmetric function, thereby providing a counterexample to a conjecture from the paper "Schur and e-positivity of trees and cut vertices".
The degree chromatic polynomial $Pm(G,k)$ of a graph $G$ counts the number of $k$-colorings in which no vertex has $m$ adjacent vertices of its same color. We prove Humpert and Martin's conjecture on the leading terms of the degree chromatic polynomial of a tree.
Among other results, it is shown that 3-trees are $Δ$-edge-choosable and that graphs of tree-width 3 and maximum degree at least 7 are $Δ$-edge-choosable.
A well-known open problem in graph theory asks whether Stanley's chromatic symmetric function, a generalization of the chromatic polynomial of a graph, distinguishes between any two non-isomorphic trees. Previous work has proven the conjecture for a class of trees called spiders. This paper generalizes the class of spiders to $n$-spiders, where normal spiders correspond to $n = 1$, and verifies the conjecture for $n = 2$.
We show that there exist linear-time algorithms that compute the strong chromatic index and a maximum induced matching of tree-cographs when the decomposition tree is a part of the input. We also show that there exist efficient algorithms for the strong chromatic index of (bipartite) permutation graphs and of chordal bipartite graphs.
The chromatic sum $Σ(G)$ of a graph $G$ is the smallest sum of colors among of proper coloring with the natural number. In this paper, we introduce a necessary condition for the existence of graph homomorphisms. Also, we present $Σ(G)<χ_f(G)|G|$ for every graph $G$.
It is a long-standing question of Stanley whether or not the chromatic symmetric function (CSF) distinguishes unrooted trees. Previously, the best computational result, due to Russell, proved that it distinguishes all trees with at most $25$ vertices. In this paper, we present a novel probabilistic algorithm which may be used to check more efficiently that the CSF distinguishes a set of trees. Applying it, we verify that the CSF distinguishes all trees with up to $29$ vertices.
In this short note, we extend the result of Galluccio, Goddyn, and Hell, which states that graphs of large girth excluding a minor are nearly bipartite. We also prove a similar result for the oriented chromatic number, from which follows in particular that graphs of large girth excluding a minor have oriented chromatic number at most $5$, and for the $p$th chromatic number $χ_p$, from which follows in particular that graphs $G$ of large girth excluding a minor have $χ_p(G)\leq p+2$.
It is proved that if $G$ is a graph containing a spanning tree with at most three leaves, then the chromatic polynomial of $G$ has no roots in the interval $(1,t_1]$, where $t_1 \approx 1.2904$ is the smallest real root of the polynomial $(t-2)^6 +4(t-1)^2(t-2)^3 -(t-1)^4$. We also construct a family of graphs containing such spanning trees with chromatic roots converging to $t_1$ from above. We employ the Whitney $2$-switch operation to manage the analysis of an infinite class of chromatic polynomials.
Some coloring algorithms gives an upper bound for the locating chromatic number of trees with all the vertices not in an end-path colored by only two colors. That means, a better coloring algorithm could be achieved by optimizing the number of colors used in the end-paths. We provide an estimation of the locating chromatic number of trees using the locating chromatic number of its end-palms. We also study the locating chromatic number of palms, a subdivision of star. We also prove $χ_L(S_n(k))=Θ(n^{1/k})$; $χ_L(S_n(3))=(1+o(1))\sqrt[3]{4n}$; and $χ_L(O_n)=\left\lceil\log_3\left(\frac{n}{4}\rig…
For a tree $T$, consider its smallest subtree $T^{\circ}$ containing all vertices of degree at least $3$. Then the remaining edges of $T$ lie on disjoint paths each with one endpoint on $T^{\circ}$. We show that the chromatic symmetric function of $T$ determines the size of $T^{\circ}$, and the multiset of the lengths of these incident paths. In particular, this generalizes a proof of Martin, Morin, and Wagner that the chromatic symmetric function distinguishes spiders.
Fong et al. (The game chromatic index of some trees with maximum degree four and adjacent degree-four vertices, J. Comb Optim 36 (2018) 1-12) proved that the game chromatic index of any tree $T$ of maximum degree 4 whose degree-four vertices induce a forest of paths of length $l$ less than 2 is at most 5. In this paper, we show that the bound 5 is also valid for $l\leq 2$. This partially solves the problem of characterization of the trees whose game chromatic index exceeds the maximum degree by at most 1, which was proposed by Cai and Zhu (Game chromatic index of $k$-degenerate graphs, J. Grap…
A star edge coloring of a graph $G$ is a proper edge coloring of $G$ such that every path and cycle of length four in $G$ uses at least three different colors. The star chromatic index of a graph $G$, is the smallest integer $k$ for which $G$ admits a star edge coloring with $k$ colors. In this paper, we present a polynomial time algorithm that finds an optimum star edge coloring for every tree. We also provide some tight bounds on the star chromatic index of trees with diameter at most four, and using these bounds we find a formula for the star chromatic index of certain families of trees.
While the game chromatic number of a forest is known to be at most 4, no simple criteria are known for determining the game chromatic number of a forest. We first state necessary and sufficient conditions for forests with game chromatic number 2 and then investigate the differences between forests with game chromatic number 3 and 4. In doing so, we present a minimal example of a forest with game chromatic number 4, criteria for determining the game chromatic number of a forest without vertices of degree 3, and an example of a forest with maximum degree 3 and game chromatic number 4.
In 2001, Brualdi and Hollingsworth proved that an edge-colored balanced complete bipartite graph Kn,n with a color set C = {1,2,3,..., 2n-1} has a heterochromatic spanning tree if the number of edges colored with colors in R is more than |R|^2 /4 for any non-empty subset R \subseteq C, where a heterochromatic spanning tree is a spanning tree whose edges have distinct colors, namely, any color appears at most once. In 2010, Suzuki generalized heterochromatic graphs to f-chromatic graphs, where any color c appears at most f(c). Moreover, he presented a necessary and sufficient condition for grap…
Let H be a tree. It was proved by Rodl that graphs that do not contain H as an induced subgraph, and do not contain the complete bipartite graph $K_{t,t}$ as a subgraph, have bounded chromatic number. Kierstead and Penrice strengthened this, showing that such graphs have bounded degeneracy. Here we give a further strengthening, proving that for every tree H, the degeneracy is at most polynomial in t. This answers a question of Bonamy, Pilipczuk, Rzazewski, Thomasse and Walczak.
A proper $k$-coloring of a graph $G=(V,E)$ is a function $c: V(G)\to \{1,\ldots,k\}$ such that $c(u)\neq c(v)$, for every $uv\in E(G)$. The chromatic number $χ(G)$ is the minimum $k$ such that there exists a proper $k$-coloring of $G$. Given a spanning subgraph $H$ of $G$, a $q$-backbone $k$-coloring of $(G,H)$ is a proper $k$-coloring $c$ of $V(G)$ such that $\lvert c(u)-c(v)\rvert \ge q$, for every edge $uv\in E(H)$. The $q$-backbone chromatic number $BBC_q(G,H)$ is the smallest $k$ for which there exists a $q$-backbone $k$-coloring of $(G,H)$. In this work, we show that every connected grap…
This paper deals with the so-called Stanley conjecture, which asks whether they are non-isomorphic trees with the same symmetric function generalization of the chromatic polynomial. By establishing a correspondence between caterpillars trees and integer compositions, we prove that caterpillars in a large class (we call trees in this class proper) have the same symmetric chromatic function generalization of the chromatic polynomial if and only if they are isomorphic.
Let $G=(V(G), E(G))$ be a multigraph with maximum degree $Δ(G)$, chromatic index $χ'(G)$ and total chromatic number $χ''(G)$. The Total Coloring conjecture proposed by Behzad and Vizing, independently, states that $χ''(G)\leq Δ(G)+μ(G) +1$ for a multigraph $G$, where $μ(G)$ is the multiplicity of $G$. Moreover, Goldberg conjectured that $χ''(G)=χ'(G)$ if $χ'(G)\geq Δ(G)+3$ and noticed the conjecture holds when $G$ is an edge-chromatic critical graph. By assuming the Goldberg-Seymour conjecture, we show that $χ''(G)=χ'(G)$ if $χ'(G)\geq \max\{ Δ(G)+2, |V(G)|+1\}$ in this note. Consequently, $χ'…
DP-coloring (also called correspondence coloring) is a generalization of list coloring recently introduced by Dvořák and Postle. Several known bounds for the list chromatic number of a graph $G$, $χ_\ell(G)$, also hold for the DP-chromatic number of $G$, $χ_{DP}(G)$. On the other hand, there are several properties of the DP-chromatic number that shows that it differs with the list chromatic number. In this note we show one such property. It is well known that $χ_\ell (K_{k,t}) = k+1$ if and only if $t \geq k^k$. We show that $χ_{DP} (K_{k,t}) = k+1$ if $t \geq 1 + (k^k/k!)(\log(k!)+1)$, and we…
The packing chromatic number $χ_ρ(G)$ of a graph $G$ is the smallest integer $k$ such that there exists a $k$-vertex coloring of $G$ in which any two vertices receiving color $i$ are at distance at least $i+1$. In this short note we present upper and lower bound for the packing chromatic number of the lexicographic product $G\circ H$ of graphs $G$ and $H$. Both bounds coincide in many cases. In particular this happens if $|V(H)|-α(H)\geq {\rm diam}(G)-1$, where $α(G)$ denotes the independence number of $G$.
We investigate the $e$-positivity and Schur positivity of the chromatic symmetric functions of some spider graphs with three legs. We obtain the positivity classification of all broom graphs and that of most double broom graphs. The methods involve extracting particular $e$-coefficients of the chromatic symmetric function of these graphs with the aid of Orellana and Scott's triple-deletion property, and using the combinatorial formula of Schur coefficients by examining certain special rim hook tabloids. We also propose some conjectures on the $e$-positivity and Schur positivity of trees.
We conjecture that any graph $G$ with treewidth~$k$ and maximum degree $Δ(G)\geq k + \sqrt{k}$ satisfies $χ'(G)=Δ(G)$. In support of the conjecture we prove its fractional version. We also show that any graph $G$ with treewidth~$k\geq 4$ and maximum degree $2k-1$ satisfies $χ'(G)=Δ(G)$, improving an old result of Vizing.
A connected $n$-chromatic graph $G$ is double-critical if for all the edges $xy$ of $G$, the graph $G-x-y$ is $(n-2)$-chromatic. In 1966, Erd\H os and Lovász conjectured that the only double-critical $n$-chromatic graph is $K_n$. This conjecture remains unresolved for $n \ge 6.$ In this short note, we verify this conjecture for claw-free graphs $G$ of chromatic number $6$.
Let $T$ be an unrooted tree. The \emph{chromatic symmetric function} $X_T$, introduced by Stanley, is a sum of monomial symmetric functions corresponding to proper colorings of $T$. The \emph{subtree polynomial} $S_T$, first considered under a different name by Chaudhary and Gordon, is the bivariate generating function for subtrees of $T$ by their numbers of edges and leaves. We prove that $S_T = <Φ,X_T>$, where $<\cdot,\cdot>$ is the Hall inner product on symmetric functions and $Φ$ is a certain symmetric function that does not depend on $T$. Thus the chromatic symmetric function is a stronge…
Let $f$ be a proper $k$-coloring of a connected graph $G$ and $Π=(V_1,V_2,\ldots,V_k)$ be an ordered partition of $V(G)$ into the resulting color classes. For a vertex $v$ of $G$, the color code of $v$ with respect to $Π$ is defined to be the ordered $k$-tuple $c_{{}_Π}(v)=(d(v,V_1),d(v,V_2),\ldots,d(v,V_k)),$ where $d(v,V_i)=\min\{d(v,x): x\in V_i\}, 1\leq i\leq k$. If distinct vertices have distinct color codes, then $f$ is called a locating coloring. The minimum number of colors needed in a locating coloring of $G$ is the locating chromatic number of $G$, denoted by $\Cchi_{{}_L}(G)$. In th…
In this work, we continue the tradition initiated by Geschke, 2011 of viewing the uncountable Borel chromatic number of analytic graphs as cardinal invariants of the continuum. We show that various uncountable Borel chromatic numbers of closed graphs can be consistently different, as well as consistently equal to the continuum. This is done using arguments that are typical to Axiom A forcing notions.
One of the major outstanding conjectures in the study of chromatic symmetric functions (CSF's) states that trees are uniquely determined by their CSF's. Though verified on graphs of order up to twenty-nine, this result has been proved only for certain subclasses of trees. Using the definition of the CSF that emerges via the Frobenius character map applied to $\mathbb{C}[S_n]$, we offer new algebraic proofs of several results about the CSF's of trees. Additionally, we prove that a "parent function" of the CSF defined in the group ring of $S_n$ can uniquely determine trees, providing further sup…
In 2006, Suzuki, and Akbari & Alipour independently presented a necessary and sufficient condition for edge-colored graphs to have a heterochromatic spanning tree, where a heterochromatic spanning tree is a spanning tree whose edges have distinct colors. In this paper, we propose $f$-chromatic graphs as a generalization of heterochromatic graphs. An edge-colored graph is $f$-chromatic if each color $c$ appears on at most $f(c)$ edges. We also present a necessary and sufficient condition for edge-colored graphs to have an $f$-chromatic spanning forest with exactly $m$ components. Moreover, usin…
A {\em chromatic root} is a root of the chromatic polynomial of a graph. While the real chromatic roots have been extensively studied and well understood, little is known about the {\em real parts} of chromatic roots. It is not difficult to see that the largest real chromatic root of a graph with $n$ vertices is $n-1$, and indeed, it is known that the largest real chromatic root of a graph is at most the tree-width of the graph. Analogous to these facts, it was conjectured in [8] that the real parts of chromatic roots are also bounded above by both $n-1$ and the tree-width of the graph. In thi…
The Gyarfas-Sumner conjecture asserts that if H is a tree then every graph with bounded clique number and very large chromatic number contains H as an induced subgraph. This is still open, although it has been proved for a few simple families of trees, including trees of radius two, some special trees of radius three, and subdivided stars. These trees all have the property that their vertices of degree more than two are clustered quite closely together. In this paper, we prove the conjecture for two families of trees which do not have this restriction. As special cases, these families contain …
We investigate which graphs H have the property that in every graph with bounded clique number and sufficiently large chromatic number, some induced subgraph is isomorphic to a subdivision of H. In an earlier paper, one of us proved that every tree has this property; and in another earlier paper with M. Chudnovsky, we proved that every cycle has this property. Here we give a common generalization. Say a banana is the union of a set of paths all with the same ends but otherwise disjoint. We prove that if H is obtained from a tree by replacing each edge by a banana then H has the property mentio…
The "clustered chromatic number" of a class of graphs is the minimum integer $k$ such that for some integer $c$ every graph in the class is $k$-colourable with monochromatic components of size at most $c$. We determine the clustered chromatic number of any minor-closed class with bounded treedepth, and prove a best possible upper bound on the clustered chromatic number of any minor-closed class with bounded pathwidth. As a consequence, we determine the fractional clustered chromatic number of every minor-closed class.
In a 1995 paper Richard Stanley defined $X_G$, the symmetric chromatic polynomial of a Graph $G=(V,E)$. He then conjectured that $X_G$ distinguishes trees; a conjecture which still remains open. $X_G$ can be represented as a certain collection of integer partitions of $|V|$ induced by each $S\subseteq E$, which is very approachable with the aid of a computer. Our research involved writing a computer program for efficient verification of this conjecture for trees up to 23 vertices. In this process, we also gather trees with matching collections of integer partitions of a fixed number of parts. …
