612 research outputs found
The -genus of Kuratowski minors
A drawing of a graph on a surface is independently even if every pair of
nonadjacent edges in the drawing crosses an even number of times. The
-genus of a graph is the minimum such that has an
independently even drawing on the orientable surface of genus . An
unpublished result by Robertson and Seymour implies that for every , every
graph of sufficiently large genus contains as a minor a projective
grid or one of the following so-called -Kuratowski graphs: , or
copies of or sharing at most common vertices. We show that
the -genus of graphs in these families is unbounded in ; in
fact, equal to their genus. Together, this implies that the genus of a graph is
bounded from above by a function of its -genus, solving a problem
posed by Schaefer and \v{S}tefankovi\v{c}, and giving an approximate version of
the Hanani-Tutte theorem on orientable surfaces. We also obtain an analogous
result for Euler genus and Euler -genus of graphs.Comment: 23 pages, 7 figures; a few references added and correcte
Correspondence scrolls
This paper initiates the study of a class of schemes that we call
correspondence scrolls, which includes the rational normal scrolls and linearly
embedded projective bundle of decomposable bundles, as well as degenerate K3
surfaces, Calabi-Yau 3-folds, and many other examples
Combinatorics of embeddings
We offer the following explanation of the statement of the Kuratowski graph
planarity criterion and of 6/7 of the statement of the Robertson-Seymour-Thomas
intrinsic linking criterion. Let us call a cell complex 'dichotomial' if to
every cell there corresponds a unique cell with the complementary set of
vertices. Then every dichotomial cell complex is PL homeomorphic to a sphere;
there exist precisely two 3-dimensional dichotomial cell complexes, and their
1-skeleta are K_5 and K_{3,3}; and precisely six 4-dimensional ones, and their
1-skeleta all but one graphs of the Petersen family.
In higher dimensions n>2, we observe that in order to characterize those
compact n-polyhedra that embed in S^{2n} in terms of finitely many "prohibited
minors", it suffices to establish finiteness of the list of all (n-1)-connected
n-dimensional finite cell complexes that do not embed in S^{2n} yet all their
proper subcomplexes and proper cell-like combinatorial quotients embed there.
Our main result is that this list contains the n-skeleta of (2n+1)-dimensional
dichotomial cell complexes. The 2-skeleta of 5-dimensional dichotomial cell
complexes include (apart from the three joins of the i-skeleta of
(2i+2)-simplices) at least ten non-simplicial complexes.Comment: 49 pages, 1 figure. Minor improvements in v2 (subsection 4.C on
transforms of dichotomial spheres reworked to include more details;
subsection 2.D "Algorithmic issues" added, etc
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