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The torsion linking pairing of a rational homology sphere is nonsingular
Statement
Assume AC. If is a closed connected oriented -manifold with finite , then the bounding-chain torsion linking pairing is symmetric and nonsingular: its adjoint is an isomorphism.
Statement references
Facts & Assumptions
Given: Full AC and a closed connected oriented -manifold with finite .
Full AC is assumed wherever the cover and orientation conventions use the choice axiom. The Axiom of Choice
Poincaré duality for closed oriented manifolds gives and . Poincaré duality for oriented topological manifolds
The cohomology universal coefficient sequence over identifies with and with , since is free. The universal coefficient theorem for cohomology over a PID
The coefficient sequence gives the long exact cohomology sequence and its natural Bockstein map . The long exact sequence in cohomology
External triangulation input. A compact topological -manifold admits a finite manifold triangulation (Moise's theorem, as stated in Aschenbrenner–Friedl–Wilton, Theorem 3.1, p. 211, under their compact-manifold convention, p. 203). We use its barycentric dual cells as a chain model, not as an additional smoothness hypothesis on . Orient a dual cell so that its oriented transverse intersection with the corresponding primal cell is positive. The dual-cell description of Poincaré duality is recalled in Hatcher, §3.3, pp. 232–233; the specific bounding-chain/Bockstein identity is proved below, rather than assumed.
Cellular homology computes singular homology for every CW complex and every abelian coefficient group. Under [A1], cellular cochains compute singular cohomology for CW pairs with local coefficients, naturally for coefficient morphisms. Apply these comparisons to the finite triangulation and its dual CW complex, the pair , and the trivial coefficient systems , and . Thus cellular cycles and bounding chains represent precisely the singular homology classes, and the cellular coefficient-sequence Bockstein and evaluation agree with their singular counterparts. Cellular homology computes singular homology Cellular cochains compute cohomology with local coefficients
Proof
Since is finite, by [F2], and by [F1]. Exactness of [F3] therefore makes an isomorphism. Write for inverse cap duality.
We first fix the intersection sign and verify independence directly. For transverse oriented -chains in an oriented -manifold, orient their intersection so that This sign follows by the outward-normal-first boundary convention in an oriented coordinate ball: taking a boundary in the second sheet passes its outward normal past the one normal direction of the first sheet. Consequently, the total signed endpoint count gives These identities extend linearly to chains; the terms on paired interior faces cancel. For a closed -chain and torsion cycle , choose and . Then , so . Thus if and , the closed chain has zero intersection with , giving . Replacing by permits replacing by and changes the quotient by the integer . Replacing by changes it by , also an integer. A change of transverse position is a chain homotopy: its prism has the moved-chain difference as boundary, so these same boundary identities apply. Hence the expression defines a pairing on the stated homology classes, independent of all these choices modulo .
To identify that pairing with the Bockstein, use [F4] and [F5] and represent by a primal cellular -cycle , and by a dual cellular -cycle . Since , there is an integral primal cellular -chain with . The dual-cell pairing gives the rational cellular -cochain on every oriented dual edge . Let be the integral cellular -cochain on the dual complex defined by . The sign convention in step 1.2 gives, for every dual -cell , There is no extra minus sign: in an oriented chart with tangent to the first coordinate and its dual -cell tangent to the second and third coordinates, . A primal -cell followed by its positive transverse dual edge likewise has intersection . These are precisely the oriented dual-cell representatives of inverse cap duality, so .
Reducing modulo gives a cocycle , because is integral. Under the natural comparison [F5], the connecting map in [F3] is constructed by lifting this cocycle to a rational cochain and taking its coboundary; therefore By step 1.2 this is also the bounding-chain expression for any representatives and any bounding multiple in the definition. Cellular representatives cause no restriction by [F5]: cellular and singular chain models represent the same classes, and changes of representatives and transverse positions have already been accounted for. Thus the precise identity is The evaluation is on the homology class , not on a cohomology class called its Poincaré dual; equivalently it is the corresponding degree- cup-product evaluation on .
Under [F2], evaluation identifies with the entire character group . The displayed identity in step 3.1 identifies the adjoint of the bounding-chain pairing with the composite of this isomorphism, , and . All three are isomorphisms, so the pairing is nonsingular. In particular its bilinearity also follows from these homomorphisms and evaluation.
For torsion classes , choose transverse representatives and chains with and . The boundary identity of step 1.2 applied to gives . Interchanging a -cycle and a -chain in an oriented -manifold changes the intersection sign by , so . Divide by and reduce modulo to obtain . This proves symmetry with the signed bounding-chain convention of the definition.
Depends on
- Bounding-chain expression for a torsion linking pairing
- Poincaré duality for oriented topological manifolds
- The universal coefficient theorem for cohomology over a PID
- The long exact sequence in cohomology
- Cellular homology computes singular homology
- Cellular cochains compute cohomology with local coefficients
- The Axiom of Choice
Used by
- A prime-power torsion linking form need not have a metabolizer Counterexample
- Torsion linking form and Casson–Gordon bordism data Definition
- A slice disk induces a metabolizer on the branched-cover linking form Lemma
- Prime-power cyclic branched covers of knots have finite first homology Lemma
- The boundary kernel of a rational homology ball is a linking metabolizer Lemma
Dependency tree · two levels
39 results within two dependency steps of this one, each drawn at its shortest distance from it. An arrow runs from a result to what uses it, so the chart reads left to right and ends at this result, which carries a heavier outline. Every node is a link to that result. Click elsewhere on the chart to enlarge it.
Sources
- Charles Livingston and Swatee Naik, Introduction to Knot Concordance (standard reference, not scraped)
- Patrick Gilmer, Slice Knots in S3 (standard reference, not scraped)
- Matthias Aschenbrenner, Stefan Friedl and Henry Wilton, Decision problems for 3-manifolds and their fundamental groups (standard reference, not scraped)
- Allen Hatcher, Algebraic Topology (standard reference, not scraped)