Given a knot in the 3-sphere, the non-orientable 4-genus or 4-dimensional crosscap number of a knot is the minimal first Betti number of non-orientable surfaces, smoothly and properly embedded in the 4-ball, with boundary the knot. In this paper, we calculate the non-orientable 4-genus of knots with crossing number 10.
We show that the equivariant and non-equivariant non-orientable 4-genus of p-periodic knots may differ, for any choice of p>1. Similar results have previously been obtained for the smooth 4-genus and non-orientable 3-genus of a periodic knot. These stand in contrast to Edmods' acclaimed result by which the equivariant and non-equivariant Seifert genus of a periodic knot agree.
The non-orientable 4-genus of a knot in the 3-sphere is defined as the smallest first Betti number of any non-orientable surface smoothly and properly embedded in the 4-ball, with boundary the given knot. We compute the non-orientable 4-genus for all knots with crossing number 8 or 9. As applications we prove a conjecture of Murakami's and Yasuhara's, and give a new lower bound for the slicing number of knot.
In formulating a non-orientable analogue of the Milnor Conjecture on the $4$-genus of torus knots, Batson developed an elegant construction that produces a smooth non-orientable spanning surface in $B^4$ for a given torus knot in $S^3$. While Lobb showed that Batson's surfaces do not always minimize the non-orientable $4$-genus, we prove that they always do minimize among surfaces that share their normal Euler number. We also completely determine the possible pairs of normal Euler number and first Betti number for non-orientable surfaces whose boundary lies in a class of torus knots for which …
We describe an example of a closed orientable 3-manifold with distinct distance three genus two Heegaard splittings. This demonstrates that the constructions of alternate genus two Heegaard splittings of closed orientable 3-manifolds described by Rubinstein and Scharlemann in their 1998 paper Genus Two Heegaard Splittings of Orientable 3-Manifolds, does not yield all alternate genus two splittings and must be augmented.
We determine the first homology group with coefficients in $H_1(N;\mathbb{Z})$ for the mapping class group of a non-orientable surface $N$ of genus three with two boundary components.
By considering negative surgeries on a knot $K$ in $S^3$, we derive a lower bound to the non-orientable slice genus $γ_4(K)$ in terms of the signature $σ(K)$ and the concordance invariants $V_i(\overline{K})$, which strengthens a previous bound given by Batson, and which coincides with Ozsváth-Stipsicz-Szabó's bound in terms of their $\upsilon$ invariant for L-space knots and quasi-alternating knots. A curious feature of our bound is superadditivity, implying, for instance, that the bound on the stable non-orientable genus is sometimes better than the one on $γ_4(K)$.
For a closed 4-manifold $X$ and a knot $K$ in the boundary of punctured $X$, we define $γ_X^0(K)$ to be the smallest first Betti number of non-orientable and null-homologous surfaces in punctured $X$ with boundary $K$. Note that $γ^0_{S^4}$ is equal to the non-orientable 4-ball genus and hence $γ^0_X$ is a generalization of the non-orientable 4-ball genus. While it is very likely that for given $X$, $γ^0_X$ has no upper bound, it is difficult to show it. In fact, even in the case of $γ^0_{S^4}$, its non-boundedness was shown for the first time by Batson in 2012. In this paper, we prove that fo…
J. Boyle classified 1-handles attached to surface-knots, that are closed and connected surfaces embedded in the Euclidean 4-space, in the case that the surfaces are oriented and 1-handles are orientable with respect to the orientations of the surfaces. In that case, the equivalence classes of 1-handles correspond to the equivalence classes of cords attached to the surface-knot, and correspond to the double cosets of the peripheral subgroup of the knot group. In this paper, we classify cords and cords with local orientations attached to (possibly non-orientable) surface-knots. And we classify 1…
In the symplectization of standard contact $3$-space, $\mathbb R \times \mathbb R^3$, it is known that an orientable Lagrangian cobordism between a Legendrian knot and itself, also known as an orientable Lagrangian endocobordism for the Legendrian knot, must have genus $0$. We show that any Legendrian knot has a non-orientable Lagrangian endocobordism, and that the crosscap genus of such a non-orientable Lagrangian endocobordism must be a positive multiple of $4$. The more restrictive exact, non-orientable Lagrangian endocobordisms do not exist for any exactly fillable Legendrian knot but do e…
We investigate when a Legendrian knot in standard contact $\mathbb{R}^3$ has a non-orientable exact Lagrangian filling. We prove analogs of several results in the orientable setting, develop new combinatorial obstructions to fillability, and determine when several families of knots have such fillings. In particular, we determine completely when an alternating knot (and more generally a plus-adequate knot) is decomposably non-orientably fillable, and classify the fillability of most torus and 3-strand pretzel knots. We also describe rigidity phenomena of decomposable non-orientable fillings, in…
The concordance genus of a knot is the least genus of any knot in its concordance class. It is bounded above by the genus of the knot, and bounded below by the slice genus, two well-studied invariants. In this paper we consider the concordance genus of 11--crossing prime knots. This analysis resolves the concordance genus of 533 of the 552 prime 11--crossing knots. The appendix to the paper gives concordance diagrams for 59 knots found to be concordant to knots of lower genus, including null-concordances for the 30 11--crossing knots known to be slice.
By considering non-orientable surfaces in the surgered manifolds, we show that the 10/3- and -10/3-Dehn surgeries on the 2-bridge knot $9_{27} = S(49,19)$ are not cosmetic, i.e., they give mutually non-homeomorphic manifolds. The knot is unknown to have no cosmetic surgeries by previously known results; in particular, by using the Casson invariant and the Heegaard Floer homology.
We describe the genus two knots which admit a genus one, one bridge position. These are divided into several families, one consists of vertical bandings of two genus one $(1,1)$-knots, other consists of vertical bandings of two cross cap number two 2-bridge knots, and the last one consists of genus two tunnel number one satellite knots.
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 there are topologically slice knots with 4-ball genus equal to one and arbitrarily large concordance genus.
It is known that knot Floer homology detects the genus and Alexander polynomial of a knot. We investigate whether knot Floer homology of $K$ detects more structure of minimal genus Seifert surfaces for $K$. We define an invariant of algebraically slice, genus one knots and provide examples to show that knot Floer homology does not detect this invariant. Finally, we remark that certain metabelian $L^2$-signatures bound this invariant from below.
Roberts proved that a family of alternating, arborescent, prime knots each have at least $2^{2n-1}$ distinct minimal genus Seifert surfaces, where $n$ is the genus of the knot in question. We give a subfamily of these knots that have exactly this many minimal genus Seifert surfaces.
Among non-alternating knots with $n\le 12$ crossings given in \cite{1} Turaev genus is not known for 191 knot. For 154 of them we show that they are almost alternating, so their Turaev genus is 1.
We exhibit an infinite family of knots with isomorphic knot Heegaard Floer homology. Each knot in this infinite family admits a nontrivial genus two mutant which shares the same total dimension in both knot Floer homology and Khovanov homology. Each knot is distinguished from its genus two mutant by both knot Floer homology and Khovanov homology as bigraded groups. Additionally, for both knot Heegaard Floer homology and Khovanov homology, the genus two mutation interchanges the groups in $δ$-gradings $k$ and $-k$.
We show that a positive braid knot has maximal topological 4-genus exactly if it has maximal signature invariant. As an application, we determine all positive braid knots with maximal topological 4-genus and compute the topological 4-genus for all positive braid knots with up to 12 crossings.
We show that for genus one knots the Alexander polynomial and the homology of the double cover branching over the knot provide obstructions to cosmetic crossings. As an application we prove the nugatory crossing conjecture for the negatively twisted, positive Whitehead doubles of all knots. We also verify the conjecture for several families of pretzel knots and all genus one knots with up to 10 crossings.
Gay and Kirby recently introduced the concept of a trisection for arbitrary smooth, oriented closed 4-manifolds, and with it a new topological invariant, called the trisection genus. This paper improves and implements an algorithm due to Bell, Hass, Rubinstein and Tillmann to compute trisections using triangulations, and extends it to non-orientable 4-manifolds. Lower bounds on trisection genus are given in terms of Betti numbers and used to determine the trisection genus of all standard simply connected PL 4-manifolds. In addition, we construct trisections of small genus directly from the sim…
In this paper, the support genus of all Legendrian right handed trefoil knots and some other Legendrian knots is computed. We give examples of Legendrian knots in the three-sphere with the standard contact structure which have positive support genus with arbitrarily negative Thurston-Benniquin invariant. This answers a question in Onaran.
The Turaev genus of a knot is a topological measure of how far a given knot is from being alternating. Recent work by several authors has focused attention on this interesting invariant. We discuss how the Turaev genus is related to other knot invariants, including the Jones polynomial, knot homology theories, and ribbon-graph polynomial invariants.
We prove the cosmetic crossing conjecture for genus one knots with non-trivial Alexander polynomial. We also prove the conjecture for genus one knots with trivial Alexander polynomial, under some additional assumptions.
We give a necessary and sufficient condition for a simple closed curve on the boundary of a genus two handlebody to decompose the handlebody into (torus with one boundary component times [0,1]. We use this condition to decide whether a simple closed curve on a genus two Heegaard surface is a GOF-knot (genus one fibered knot) which induces the Heegaard splitting. By using this, we determine the number and the positions with respect to the Heegaard splittings of GOF-knots in the 3-manifolds with reducible genus two Heegaard splittings. This is another proof of results of Morimoto and Baker.
We show that the triple-crossing number of any knot is greater or equal to twice its (canonical) genus and we show an even stronger bound in the case of links. As an application we show that this bound is strong enough to obtain the triple-crossing numbers of all torus knots, and of many more knots and their connected sums.
We compute the smooth 4-genera of the prime knots with 12 crossings whose values, as reported on the KnotInfo website, were unknown. This completes the calculation of the smooth 4-genus for all prime knots with 12 or fewer crossings.
The genus of knots is a one of the fundamental invariant and can be seen as a complexity of knots. In this paper, we give a lower bound of genus using Dehornoy floor, which is a measure of complexity of braids in terms of braid ordering.
Let $N_g$ be the non-orientable surface with genus $g$, $\text{MCG}(N_g)$ be the mapping class group of $N_g$, $\mathcal{T}(N_g)$ be the index 2 subgroup generated by all Dehn twists of $\text{MCG}(N_g)$. We prove that for odd genus, $\mathcal{T}(N_g)$ can be generated by three elements of finite orders.
We give an obstruction for genus one knots $K$, $K'$ to have the Gordian distance one by using the $0$th coefficient of the HOMFLT polynomials. As an application, we give a new constraint for genus one knot to admit a (generalized) cosmetic crossing. Combining known results, we prove the (generalized) cosmetic crossing conjecture for genus one pretzel knots.
Morifuji computed the twisted Alexander polynomial of twist knots for nonabelian representations. In this paper we compute the twisted Alexander polynomial and the Reidemeister torsion of genus one two-bridge knots, a class of knots which includes twist knots. As an application, we give a formula for the Reidemeister torsion of the 3-manifold obtained by a Dehn surgery on a genus one two-bridge knot.
A knot K is called a 1-genus 1-bridge knot in a 3-manifold M if (M,K) has a Heegaard splitting (V_1,t_1)\cup (V_2,t_2) where V_i is a solid torus and t_i is a boundary parallel arc properly embedded in V_i. If the exterior of a knot has a genus 2 Heegaard splitting, we say that the knot has an unknotting tunnel. Naturally the exterior of a 1-genus 1-bridge knot K allows a genus 2 Heegaard splitting, i.e., K has an unknotting tunnel. But, in general, there are unknotting tunnels which are not derived form this procedure. Some of them may be levelled with the torus \partial V_1=\partial V_2, who…