arXiv research

Developed an ellipsoidal density-equalizing map for genus-0 closed surfaces.

An oriented link is positive if it has a link diagram whose crossings are all positive. An oriented link is almost positive if it is not positive and has a link diagram with exactly one negative crossing. It is known that the Rasmussen invariant, $4$-genus and $3$-genus of a positive knot are equal. In this paper, we p…

Develops spherical density-equalizing maps for closed surfaces.

In this paper we write explicitly the open book decompositions of links of quotient surface singularities supporting the corresponding unique Milnor fillable contact structure. The page-genus of these Milnor open books are minimal among all Milnor open books supporting the same contact structure. We also investigate wh…

The virtual genus of a virtual satellite link is equal to that of its companion.

Construct divide knots with specific genus properties.

Minimal hitting time on origami equals diophantine type for certain slopes.

Using the theory of hyperbolic manifolds with totally geodesic boundary, we provide for every integer n greater than 1 a class of such manifolds all having Matveev complexity equal to n and Heegaard genus equal to n+1. All the elements of this class have a single boundary component of genus n, and the numbers of distin…

The concordance genus of a knot K is the minimum Seifert genus of all knots smoothly concordant to K. Concordance genus is bounded below by the 4-ball genus and above by the Seifert genus. We give a lower bound for the concordance genus of K coming from the knot Floer complex of K. As an application, we prove that ther…

Investigates minimal genus of second homology classes in RAAGs, finding bounds and specific cases.

A knot K in 1-bridge position with respect to a genus-g Heegaard surface in a 3-manifold can be moved by isotopy through knots in 1-bridge position until it lies in a union of n parallel genus-g surfaces tubed together by n-1 straight tubes, with K intersecting each tube in two arcs connecting the ends. We prove that t…

We show that {\sc Heegaard Genus $\leq g$}, the problem of deciding whether a triangulated 3-manifold admits a Heegaard splitting of genus less than or equal to $g$, is NP-hard. The result follows from a quadratic time reduction of the NP-complete problem {\sc CNF-SAT} to {\sc Heegaard Genus $\leq g$}.

For $d\geq 2$, the regular genus of a closed connected PL $d$-manifold $M$ is the least genus (resp., half of the genus) of an orientable (resp., a non-orientable) surface into which a crystallization of $M$ imbeds regularly. The regular genus of every orientable surface equals its genus, and the regular genus of every…

A geometric argument is given to prove that the Seifert genus of a positive knot equals its slice genus. A combinatorial invariant, giving a lower bound for the slice genus, is formulated for arbitrary knots. Properties and applications of this invariant are discussed.

The signature of a surface bundle over a surface is known to be divisible by 4. It is also known that the signature vanishes if the fiber genus is less than or equal to 2 or the base genus is less than or equal to 1. In this article, we construct new smooth 4-manifolds with signature 4 which are surface bundles over su…

There exists a properly embedded minimal surface of genus one with one end. The end is asymptotic to the end of the helicoid. This genus one helicoid is constructed as the limit of a continuous one-parameter family of screw-motion invariant minimal surfaces--also asymptotic to the helicoid--that have genus equal to one…

We prove that if $M$ is a three-manifold with scalar curvature greater than or equal to -2 and $Σ\subset M$ is a two-sided compact embedded Riemann surface of genus greater than 1 which is locally area-minimizing, then the area of $Σ$ is greater than or equal to $4π(g(Σ)-1)$, where $g(Σ)$ denotes the genus of $Σ$. In t…

We show that for every sequence $(n_i)$, where each $n_i$ is either an integer greater than 1 or is $\infty$, there exists a simply connected open 3-manifold $M$ with a countable dense set of ends $\{e_i\}$ so that, for every $i$, the genus of end $e_i$ is equal to $n_i$. In addition, the genus of the ends not in the d…

New findings on generating mapping class groups using pseudo-Anosov elements.

The Horikawa index and the local signature are introduced for relatively minimal fibered surfaces whose general fiber is a non-hyperelliptic curve of genus $4$ with unique trigonal structure.

Characterizes the Z-genus of boundary links using Blanchfield forms.

We show that, if g is more than or equal to 2, the virtual cohomological dimension of the mapping class group of a 3-dimensional handlebody of genus g is equal to 4g-5 and the Euler number of it is equal to 0.

An estimate for the genus function in circle bundles over irreducible 3-manifolds is proven. This estimate is in many cases an equality and it relates the minimal genus of the surfaces representing a given homology class with the self-intersection of the class and the Thurston norm of the underlying 3-manifold.

Simple proof of knot genus theorem using Alexander polynomial.

Local knots can't bound smaller surfaces in rational homology 3-spheres.

The paper resolves conjectures about knot invariants and shows infinite families of knots.

The paper calculates genus bounds for multibranched surfaces.

We found an infinite family of counterexamples to Batson's conjecture.

The study classifies certain types of incomplete surfaces with low curvature.

New knots found that are 4-genus minimal.

The unknotting number of a knot is bounded from below by its slice genus. It is a well-known fact that the genera and unknotting numbers of torus knots coincide. In this note we characterize quasipositive knots for which the genus bound is sharp: the slice genus of a quasipositive knot equals its unknotting number, if …

The strong symmetric genus of a finite group is the minimum genus of a compact Riemann surface on which the group acts as a group of automorphisms preserving orientation. A characterization of the infinite number of groups with strong symmetric genus zero and one is well-known and the problem is finite for each strong …

We study the existence of incompressible embeddings of surfaces into the genus two handlebody. We show that for every compact surface with boundary, orientable or not, there is an incompressible embedding of the surface into the genus two handlebody. In the orientable case the embedding can be either separating or non-…

A classical result states that the determinant of an alternating link is equal to the number of spanning trees in a checkerboard graph of an alternating connected projection of the link. We generalize this result to show that the determinant is the alternating sum of the number of quasi-trees of genus j of the dessin o…

There exists a (relatively minimal) genus g Lefschetz fibration with only one singular fiber over a closed (Riemann) surface of genus h iff g>2 and h>1. The singular fiber can be chosen to be reducible or irreducible. Other results are that every Dehn twist on a closed surface of genus at least three is a product of tw…

New lower bound for knot genus using Links-Gould invariant.

We show that on a nonorientable surface of genus at least 7 any power of a Dehn twist is equal to a single commutator in the mapping class group and the same is true, under additional assumptions, for the twist subgroup, and also for the extended mapping class group of an orientable surface of genus at least 3.

We show that the mapping class group of a closed oriented surface of genus at least three is generated by 3 elements of order 3 and by 4 elements of order 4. Note that the mapping class group cannot be generated by finitely many torsion elements of same order if genus is equal to one or two.

Triple-crossing number bound for knots and links, especially torus knots.

Same-genus Seifert surfaces for non-split alternating links are smoothly isotopic.

Upper bounds on area for surfaces with constant mean curvature in hyperbolic 3-manifolds.

It is known that the minimal degree of the Jones polynomial of a positive knot is equal to its genus, and the minimal coefficient is 1. We extend this result to almost positive links and partly identify the 3 following coefficients for special types of positive links. We also give counterexamples to the Jones polynomia…

In this article we study the asymptotic behavior of small eigenvalues of Riemann surfaces for large genus. We show that for any positive integer $k$, as the genus $g$ goes to infinity, the smallest $k$-th eigenvalue of Riemann surfaces in any thick part of moduli space of Riemann surfaces of genus $g$ is uniformly comp…

It is a conjecture that the signature of a positive link is bounded below by an increasing function of its negated Euler characteristic. In relation to this conjecture, we apply the generator description for canonical genus to show that the boundedness of the genera of positive knots with given signature can be algorit…

Elliptic surfaces have unique Lefschetz pencils and Calabi-Yau diffeomorphisms.

The first nontrivial eigenvalue of the Laplacian can be considered as a functional on the space of all Riemannian metrics of unit volume on a fixed surface. In this paper we prove that for the surface of genus 2 the supremum of this functional is equal to $16π$. This provides a positive answer to the conjecture by Jako…

We show that for many strata of Abelian differentials in low genus the sum of Lyapunov exponents for the Teichmueller geodesic flow is the same for all Teichmueller curves in that stratum, hence equal to the sum of Lyapunov exponents for the whole stratum. This behavior is due to the disjointness property of Teichmuell…

Lower bounds on rational slice genus using Heegaard Floer invariants.