120 research outputs found

    Weak splittings of quotients of Drinfeld and Heisenberg doubles

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    We investigate the fine structure of the simplectic foliations of Poisson homogeneous spaces. Two general results are proved for weak splittings of surjective Poisson submersions from Heisenberg and Drinfeld doubles. The implications of these results are that the torus orbits of symplectic leaves of the quotients can be explicitly realized as Poisson-Dirac submanifolds of the torus orbits of the doubles. The results have a wide range of applications to many families of real and complex Poisson structures on flag varieties. Their torus orbits of leaves recover important families of varieties such as the open Richardson varieties.Comment: 20 pages, AMS Late

    Quantum cohomology via vicious and osculating walkers

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    We relate the counting of rational curves intersecting Schubert varieties of the Grassmannian to the counting of certain non-intersecting lattice paths on the cylinder, so-called vicious and osculating walkers. These lattice paths form exactly solvable statistical mechanics models and are obtained from solutions to the Yang–Baxter equation. The eigenvectors of the transfer matrices of these models yield the idempotents of the Verlinde algebra of the gauged u^(n)k -WZNW model. The latter is known to be closely related to the small quantum cohomology ring of the Grassmannian. We establish further that the partition functions of the vicious and osculating walker model are given in terms of Postnikov’s toric Schur functions and can be interpreted as generating functions for Gromov–Witten invariants. We reveal an underlying quantum group structure in terms of Yang–Baxter algebras and use it to give a generating formula for toric Schur functions in terms of divided difference operators which appear in known representations of the nil-Hecke algebra

    On Landau-Ginzburg models for quadrics and flat sections of Dubrovin connections

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    This paper proves a version of mirror symmetry expressing the (small) Dubrovin connection for even-dimensional quadrics in terms of a mirror-dual Landau–Ginzburg model View the MathML source(X?can,Wq). Here X?can is the complement of an anticanonical divisor in a Langlands dual quadric. The superpotential Wq is a regular function on X?can and is written in terms of coordinates which are naturally identified with a cohomology basis of the original quadric. This superpotential is shown to extend the earlier Landau–Ginzburg model of Givental, and to be isomorphic to the Lie-theoretic mirror introduced in [36]. We also introduce a Laurent polynomial superpotential which is the restriction of Wq to a particular torus in X?can. Together with results from [31] for odd quadrics, we obtain a combinatorial model for the Laurent polynomial superpotential in terms of a quiver, in the vein of those introduced in the 1990's by Givental for type A full flag varieties. These Laurent polynomial superpotentials form a single series, despite the fact that our mirrors of even quadrics are defined on dual quadrics, while the mirror to an odd quadric is naturally defined on a projective space. Finally, we express flat sections of the (dual) Dubrovin connection in a natural way in terms of oscillating integrals associated to View the MathML source(X?can,Wq) and compute explicitly a particular flat section

    Generalizing Tanisaki's ideal via ideals of truncated symmetric functions

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    We define a family of ideals IhI_h in the polynomial ring Z[x1,...,xn]\mathbb{Z}[x_1,...,x_n] that are parametrized by Hessenberg functions hh (equivalently Dyck paths or ample partitions). The ideals IhI_h generalize algebraically a family of ideals called the Tanisaki ideal, which is used in a geometric construction of permutation representations called Springer theory. To define IhI_h, we use polynomials in a proper subset of the variables x1,...,xn{x_1,...,x_n} that are symmetric under the corresponding permutation subgroup. We call these polynomials {\em truncated symmetric functions} and show combinatorial identities relating different kinds of truncated symmetric polynomials. We then prove several key properties of IhI_h, including that if h>h′h>h' in the natural partial order on Dyck paths then Ih⊂Ih′I_{h} \subset I_{h'}, and explicitly construct a Gr\"{o}bner basis for IhI_h. We use a second family of ideals JhJ_h for which some of the claims are easier to see, and prove that Ih=JhI_h = J_h. The ideals JhJ_h arise in work of Ding, Develin-Martin-Reiner, and Gasharov-Reiner on a family of Schubert varieties called partition varieties. Using earlier work of the first author, the current manuscript proves that the ideals Ih=JhI_h = J_h generalize the Tanisaki ideals both algebraically and geometrically, from Springer varieties to a family of nilpotent Hessenberg varieties.Comment: v1 had 27 pages. v2 is 29 pages and adds Appendix B, where we include a recent proof by Federico Galetto of a conjecture given in the previous version. We also add some connections between our work and earlier results of Ding, Gasharov-Reiner, and Develin-Martin-Reiner. v3 corrects a typo in Valibouze's citation in the bibliography. To appear in Journal of Algebraic Combinatoric

    Depletion of Plasmodium berghei Plasmoredoxin Reveals a Non-Essential Role for Life Cycle Progression of the Malaria Parasite

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    Proliferation of the pathogenic Plasmodium asexual blood stages in host erythrocytes requires an exquisite capacity to protect the malaria parasite against oxidative stress. This function is achieved by a complex antioxidant defence system composed of redox-active proteins and low MW antioxidants. Here, we disrupted the P. berghei plasmoredoxin gene that encodes a parasite-specific 22 kDa member of the thioredoxin superfamily. The successful generation of plasmoredoxin knockout mutants in the rodent model malaria parasite and phenotypic analysis during life cycle progression revealed a non-vital role in vivo. Our findings suggest that plasmoredoxin fulfils a specialized and dispensable role for Plasmodium and highlights the need for target validation to inform drug development strategies
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