arXiv research

Study on signatures of positive braids with bounds derived.

Positive braids have a signature bound by their Betti number.

New lower bounds on the unknotting number of a knot are constructed from the classical knot signature function. These bounds can be twice as strong as previously known signature bounds. They can also be stronger than known bounds arising from Heegaard Floer and Khovanov homology. Results include new bounds on the Gordi…

A bound on knot unknotting using equivariant signature.

We provide the optimal linear bound for the signature of positive four-braids in terms of the three-genus of their closures. As a consequence, we improve previously known linear bounds for the signature in terms of the first Betti number for all positive braid links. We obtain our results by combining bounds for positi…

Surface bundles' signatures tied to their Euler characteristics.

The paper extends graph signatures to Klein graphs and foams, linking signatures to knot properties.

Sharp signature bound for 3-strand torus knots proved.

We refine prior bounds on how the multivariable signature and the nullity of a link change under link cobordisms. The formula generalizes a series of results about the 4-genus having their origins in the Murasugi-Tristram inequality, and at the same time extends previously known results about concordance invariance of …

New lower bound for doubly slice genus using knot signatures.

Lower bound on stable 4-genus of knots using Casson-Gordon signatures.

We provide linear lower bounds for the signature of positive braids in terms of the three genus of their braid closure. This yields linear bounds for the topological slice genus of knots that arise as closures of positive braids.

Uniformly proves index invariance for signature operators on manifolds.

Average signature of 2-bridge knots approximates sqrt(2c/π).

By a theorem of A'Campo, the eigenvalues of certain Coxeter transformations are positive real or lie on the unit circle. By optimally bounding the signature of tree-like positive Hopf plumbings from below by the genus, we prove that at least two thirds of them lie on the unit circle. In contrast, we show that for divid…

The paper develops methods for novelty detection on path space using signature-based statistics.

We give bounds on knot signature, the Ozsvath-Szabo tau invariant, and the Rasmussen s invariant in terms of the Turaev genus of the knot.

Skeletal signatures were introduced in [J W Anderson and A Wootton, A Lower Bound for the Number of Group Actions on a Compact Riemann Surface, Algebr. Geom. Topol. 12 (2012) 19--35.] as a tool to describe the space of all signatures with which a group can act on a surface of genus $σ\geq 2$. In the present paper we pr…

The first aim of this paper is to give four types of examples of surface bundles over surfaces with non-zero signature. The first example is with base genus 2, a prescribed signature, a 0-section and the fiber genus greater than a certain number which depends on the signature. This provides a new upper bound on the min…

This article introduces planar shape signatures derived from homology nerves, which are intersecting 1-cycles in a collection of homology groups endowed with a proximal relator (set of nearness relations) that includes a descriptive proximity. A 1-cycle is a closed, connected path with a zero boundary in a simplicial c…

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…

Estimates path-valued data using signature metrics and local kernels.

We introduce a new method to measure model risk using optimal transport on path signatures.

Novel framework synthesizes stochastic trajectories with anticipated structural breaks.

Introduces Exponentially Weighted Signature for better path representation.

The paper adapts differential signatures to algebraic curves under group actions.

In this paper, we use `generalized Seifert surfaces' to extend the Levine-Tristram signature to colored links in S^3. This yields an integral valued function on the m-dimensional torus, where m is the number of colors of the link. The case m=1 corresponds to the Levine-Tristram signature. We show that many remarkable p…

Framework uses optimal transport to quantify model risk in stochastic path laws.

This paper continues math.DG/9903140. Here we construct a linking form on the torsion part of middle dimensional extended L^2 homology and cohomology of odd-dimensional manifolds. We give a geometric necessary condition when this linking form is hyperbolic. We compute this linking form in case when the manifold bounds.…

Reconstructing signature features from randomized vector fields in differential equations.

A new neural network model reduces features in high-dimensional sequential data.

We relate the spectral flow to the index for paths of selfadjoint Breuer-Fredholm operators affiliated to a semifinite von Neumann algebra, generalizing results of Robbin-Salamon and Pushnitski. Then we prove the vanishing of the von Neumann spectral flow for the tangential signature operator of a foliated manifold whe…

The dihedral genus of a knot is related to its signature and minimal surface genus.

Study shows bounds on symplectic fillings for spinal open book decompositions.

We use the knot filtration on the Heegaard Floer complex to define an integer invariant tau(K) for knots. Like the classical signature, this invariant gives a homomorphism from the knot concordance group to Z. As such, it gives lower bounds for the slice genus (and hence also the unknotting number) of a knot; but unlik…

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…

Generative model for TPPs using signatures and distributional discrepancies.

The nonorientable four-ball genus of a knot K is the smallest first Betti number of any smoothly embedded, nonorientable surface F in B^4 bounding K. In contrast to the orientable four-ball genus, which is bounded below by the Murasugi signature, the Ozsvath-Szabo tau-invariant, the Rasmussen s-invariant, the best lowe…

We construct examples of Lefschetz fibrations with prescribed singular fibers. By taking differences of pairs of such fibrations with the same singular fibers, we obtain new examples of surface bundles over surfaces with non-zero signature. From these we derive new upper bounds for the minimal genus of a surface repres…

New knots with specific properties have larger 4-genus than previously known bounds.

Signature volatility models are analyzed for existence, arbitrage, completeness, and hedging-error decomposition.

The paper explores stability properties of cohomology groups and norms in symplectic and mapping class groups.

New bounds on HOMFLY polynomial for homogeneous links.

A compactness theorem is proved for a family of Kähler surfaces with constant scalar curvature and volume bounded from below, diameter bounded from above, Ricci curvature bounded and the signature bounded from below. Furthermore, a splitting theorem and some rigidity theorems are proved for Einstein-Maxwell systems.

New complexity measure for shake-slice knots established.

PSLR classifies functional data with scalar covariates using path signatures.

We introduce Tristram-Levine signatures of virtual knots and use them to investigate virtual knot concordance. The signatures are defined first for almost classical knots, which are virtual knots admitting homologically trivial representations. The signatures and $ω$-signatures are shown to give bounds on the topologic…

We prove that the number of distinct group actions on compact Riemann surfaces of a fixed genus $σ\geq 2$ is at least quadratic in $σ$. We do this through the introduction of a coarse signature space, the space $\mathcal{K}_σ$ of {\em skeletal signatures} of group actions on compact Riemann surfaces of genus $σ$. We di…