Monodromy for principal bundles

Given a strongly semistable principal bundle E_G over a curve, in Biswas et al. (2006) [4], a group-scheme for it was constructed, which was named as the monodromy group-scheme. Here we extend the construction of the monodromy group-scheme to principal bundles over higher dimensional varieties.     

Inverting linear combinations of identity and generalized Catalan matrices

We introduce the notion of the generalized Catalan matrix as a kind of lower triangular Toeplitz matrix whose nonzero elements involve the generalized Catalan numbers. Inverse of the linear combination of the Pascal matrix with the identity matrix is computed in Aggarwala and Lamoureux (2002) [1]. In this paper, continuing this idea, we invert various linear combinations of the generalized Catalan matrix with the identity matrix. A simple and efficient approach to invert the Pascal matrix plus one in terms of the Hadamard product of the Pascal matrix and appropriate lower triangular Toeplitz matrices is considered in Yang and Liu (2006) [14]. We derive representations for inverses of linear combinations of the generalized Catalan matrix and the identity matrix, in terms of the Hadamard product which includes the Generalized Catalan matrix and appropriate lower triangular Toeplitz matrix.     

Quasicomplete factorizations of rational matrix functions

It is shown that within the class ofn×n rational matrix functions which are analytic at infinity with valueW()=I _n, any rational matrix functionW is the productW=W ₁...W _p of rational matrix functionsW ₁,...,W _p of McMillan degree one. Furthermore, such a factorization can be established with a number of factors not exceeding 2(W)–1, where (W) denotes the McMillan degree ofW.     

Commutativity of operators on the lattice of existence varieties

In a previous paper the authors introduced seven complete congruences on the lattice _ev(I of e-varieties of regular semigroups of the form _P :U _P VPU=PV, whereP is drawn from a small set of e-varieties: left zero, right zero, rectangular bands, groups, left groups, right groups and completely simple semigroups. Four new complete congruences are introduced here of the form _P :U _P VPU=PV, whereP is one of the following classes of regular semigroups: left monoids, right monoids, monoids, idempotent generated semigroups. For each complete congruence on _ev(I) and eachU_ev(I), the -class ofU is an interval [U ,U ] so that there is associated with each such congruence an idempotent operatorUU on _ev(I). This paper establishes numerous results concerning the commutativity of operators of this form.This work was supported in part by NSERC Grant 4044.     

The First in Vivo Observation of C–N Coupling in Mammalian Brain

[5-¹³C,¹⁵N]Glutamine, with ¹J(¹³C–¹⁵N) of 16 Hz, was observed in vivo in the brain of spontaneously breathing rats by ¹³C MRS at 4.7 T. The brain [5-¹³C]glutamine peak consisted of the doublet from [5-¹³C,¹⁵N]glutamine and the center [5-¹³C,¹⁴N]glutamine peak, resulting in an apparent triplet with a separation of 8 Hz. The time course of formation of brain [5-¹³C,¹⁵N]glutamine was monitored in vivo with a time resolution of 20–35 min. This [5-¹³C,¹⁵N]glutamine was formed by glial uptake of released neurotransmitter [5-¹³C]glutamate and its reaction with ¹⁵NH₃ catalyzed by the glia-specific glutamine synthetase. The neurotransmitter glutamate C5 was selectively¹³C-enriched by intravenous [2,5-¹³C]glucose infusion to ¹³C-label whole-brain glutamate C5, followed by [¹²C]glucose infusion to chase ¹³C from the small and rapidly turning-over glial glutamate pool, leaving ¹³C mainly in the neurotransmitter [5-¹³C]glutamate pool, which is sequestered in vesicles until release. Hence, the observed [5-¹³C,¹⁵N]glutamine arises from a coupling between ¹³C of neuronal origin and ¹⁵N of glial origin. Measurement of the rate of brain [5-¹³C,¹⁵N]glutamine formation provides a novel noninvasive method of studying the kinetics of neurotransmitter uptake into glia in vivo, a process that is crucial for protecting the brain from glutamate excitotoxicity.     

A mixed finite element method for solving the nonstationary stokes equation

Summary This paper deals with a mixed finite element method for approximating a fourth order initial value problem arising from the nonstationary Stokes problem. For piecewise linear shape functions error estimates are given with convergence rates similar to the elliptic case. Some numerical computations will illustrate the theoretical results.     

On the construction of a class of invariant polynomials in several matrices,extending the zonal polynomials

Summary The construction of a class of invariant polynomials in several matrices extending the zonal polynomials is discussed. The method adopted generalized the orginal group-theoretic approach of James [9]. A table of three-matrix polynomials up to degree 5 is presented. CSIRO     

C, N CPMAS NMR and GIAO DFT calculations of stereoisomeric oxindole alkaloids from Cat's Claw (Uncaria tomentosa)

Oxindole alkaloids, isolated from the bark of Uncaria tomentosa [Willd. ex Schult.] Rubiaceae, are considered to be responsible for the biological activity of this herb. Five pentacyclic and two tetracyclic alkaloids were studied by solid-state NMR and theoretical GIAO DFT methods. The ¹³C and ¹⁵N CPMAS NMR spectra were recorded for mitraphylline, isomitraphylline, pteropodine (uncarine C), isopteropodine (uncarine E), speciophylline (uncarine D), rhynchophylline and isorhynchophylline. Theoretical GIAO DFT calculations of shielding constants provide arguments for identification of asymmetric centers and proper assignment of NMR spectra. These alkaloids are 7R/7S and 20R/20S stereoisomeric pairs. Based on the ¹³C CP MAS chemical shifts the 7S alkaloids (δ C3 70–71 ppm) can be easily and conveniently distinguished from 7R (δC3 74.5–74.9 ppm), also 20R (δC20 41.3–41.7 ppm) from the 20S (δC20 36.3–38.3 ppm). The epiallo-type isomer (3R, 20S) of speciophylline is characterized by a larger ¹⁵N MAS chemical shift of N4 (64.6 ppm) than the allo-type (3S, 20S) of isopteropodine (δN4 53.3 ppm). ¹⁵N MAS chemical shifts of N1–H in pentacyclic alkaloids are within 131.9–140.4 ppm.     

Lee–Yang Problems and the Geometry of Multivariate Polynomials

We describe all linear operators on spaces of multivariate polynomials preserving the property of being non-vanishing in open circular domains. This completes the multivariate generalization of the classification program initiated by Pólya–Schur for univariate real polynomials and provides a natural framework for dealing in a uniform way with Lee–Yang type problems in statistical mechanics, combinatorics, and geometric function theory.