597 research outputs found

    Affine descents and the Steinberg torus

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    Let WLW\ltimes L be an irreducible affine Weyl group with Coxeter complex Σ\Sigma, where WW denotes the associated finite Weyl group and LL the translation subgroup. The Steinberg torus is the Boolean cell complex obtained by taking the quotient of Σ\Sigma by the lattice LL. We show that the ordinary and flag hh-polynomials of the Steinberg torus (with the empty face deleted) are generating functions over WW for a descent-like statistic first studied by Cellini. We also show that the ordinary hh-polynomial has a nonnegative γ\gamma-vector, and hence, symmetric and unimodal coefficients. In the classical cases, we also provide expansions, identities, and generating functions for the hh-polynomials of Steinberg tori.Comment: 24 pages, 2 figure

    Affine descents and the Steinberg torus

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    Abstract. Let W ⋉ L be an irreducible affine Weyl group with Coxeter complex Σ, where W denotes the associated finite Weyl group and L the translation subgroup. The Steinberg torus is the Boolean cell complex obtained by taking the quotient of Σ by the lattice L. We show that the ordinary and flag h-polynomials of the Steinberg torus (with the empty face deleted) are generating functions over W for a descent-like statistic first studied by Cellini. We also show that the ordinary h-polynomial has a nonnegative γ-vector, and hence, symmetric and unimodal coefficients. In the classical cases, we also provide expansions, identities, and generating functions for the h-polynomials of Steinberg tori. Résumé. Nous considérons un groupe de Weyl affine irréductible W ⋉ L avec complexe de Coxeter Σ, où W désigne le groupe de Weyl fini associé et L le sous-groupe des translations. Le tore de Steinberg est le complexe cellulaire Booléen obtenu comme le quotient de Σ par L. Nous montrons que les h-polynômes, ordinaires et de drapeaux, du tore de Steinberg (sans la face vide) sont des fonctions génératrices sur W pour une statistique de type descente, étudiée en premier lieu par Cellini. Nous montrons également qu’un h-polynôme ordinaire possède un γ-vecteur positif, et par conséquent, a des coéfficients symétriques et unimodaux. Dans les cas classiques, nous donnons également des développements, des identités et des fonctions génératrices pour les h-polynômes des tores de Steinberg

    Affine descents and the Steinberg torus

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    Let WLW \ltimes L be an irreducible affine Weyl group with Coxeter complex Σ\Sigma, where WW denotes the associated finite Weyl group and LL the translation subgroup. The Steinberg torus is the Boolean cell complex obtained by taking the quotient of Σ\Sigma by the lattice LL. We show that the ordinary and flag hh-polynomials of the Steinberg torus (with the empty face deleted) are generating functions over WW for a descent-like statistic first studied by Cellini. We also show that the ordinary hh-polynomial has a nonnegative γ\gamma-vector, and hence, symmetric and unimodal coefficients. In the classical cases, we also provide expansions, identities, and generating functions for the hh-polynomials of Steinberg tori

    Age structure, dispersion and diet of a population of stoats (Mustela erminea) in southern Fiordland during the decline phase of the beechmast cycle

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    The dispersion, age structure and diet of stoats (Mustela erminea) in beech forest in the Borland and Grebe Valleys, Fiordland National Park, were examined during December and January 2000/01, 20 months after a heavy seed-fall in 1999. Thirty trap stations were set along a 38-km transect through almost continuous beech forest, at least 1 km apart. Mice were very scarce (nights, C/100TN) along two standard index lines placed at either end of the transect, compared with November 1999 (>60/100TN), but mice were detected (from footprints in stoat tunnels) along an 8 km central section of the transect (stations 14-22). Live trapping with one trap per station (total 317.5 trap nights) in December 2000 caught 2 female and 23 male stoats, of which 10 (including both females) were radio collared. The minimum range lengths of the two females along the transect represented by the trap line were 2.2 and 6.0 km; those of eight radio-tracked males averaged 2.9 ± 1.7 km. Stations 14-22 tended to be visited more often, by more marked individual stoats, than the other 21 stations. Fenn trapping at the same 30 sites, but with multiple traps per station (1333.5 trap nights), in late January 2001 collected carcasses of 35 males and 28 females (including 12 of the marked live-trapped ones). Another two marked males were recovered dead. The stoat population showed no sign of chronic nutritional stress (average fat reserve index = 2.8 on a scale of 1-4 where 4 = highest fat content); and only one of 63 guts analysed was empty. Nevertheless, all 76 stoats handled were adults with 1-3 cementum annuli in their teeth, showing that reproduction had failed that season. Prey categories recorded in descending frequency of occurrence were birds, carabid beetle (ground beetle), weta, possum, rat, and mouse. The frequencies of occurrence of mice and birds in the diet of these stoats (10% and 48%, respectively) were quite different from those in stoats collected in Pig Creek, a tributary of the Borland River (87%, 5%), 12 months previously when mice were still abundant. Five of the six stoat guts containing mice were collected within 1 km of stations 14-22

    Observation of Beam Spin Asymmetries in the Process ep → e\u27π⁺π⁻ X with CLAS 12

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    The observation of beam spin asymmetries in two-pion production in semi-inclusive deep inelastic scattering off an unpolarized proton target is reported. The data presented here were taken in the fall of 2018 with the CLAS12 spectrometer using a 10.6 GeV longitudinally spin-polarized electron beam delivered by CEBAF at JLab. The measured asymmetries provide the first opportunity to extract the parton distribution function e(x), which provides information about the interaction between gluons and quarks, in a collinear framework that offers cleaner access than previous measurements. The asymmetries also constitute the first ever signal sensitive to the helicity-dependent two-pion fragmentation function G⊥1. A clear sign change is observed around the ρ mass that appears in model calculations and is indicative of the dependence of the produced pions on the helicity of the fragmenting quark
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