Hopf algebras and characters of classical groups

Schur functions provide an integral basis of the ring of symmetric functions. It is shown that this ring has a natural Hopf algebra structure by identifying the appropriate product, coproduct, unit, counit and antipode, and their properties. Characters of covariant tensor irreducible representations of the classical groups GL(n), O(n) and Sp(n) are then expressed in terms of Schur functions, and the Hopf algebra is exploited in the determination of group-subgroup branching rules and the decomposition of tensor products. The analysis is carried out in terms of n-independent universal characters. The corresponding rings, CharGL, CharO and CharSp, of universal characters each have their own natural Hopf algebra structure. The appropriate product, coproduct, unit, counit and antipode are identified in each case.Comment: 9 pages. Uses jpconf.cls and jpconf11.clo. Presented by RCK at SSPCM'07, Myczkowce, Poland, Sept 200

Products, coproducts and singular value decomposition

Products and coproducts may be recognized as morphisms in a monoidal tensor category of vector spaces. To gain invariant data of these morphisms, we can use singular value decomposition which attaches singular values, ie generalized eigenvalues, to these maps. We show, for the case of Grassmann and Clifford products, that twist maps significantly alter these data reducing degeneracies. Since non group like coproducts give rise to non classical behavior of the algebra of functions, ie make them noncommutative, we hope to be able to learn more about such geometries. Remarkably the coproduct for positive singular values of eigenvectors in $A$ yields directly corresponding eigenvectors in A\otimes A.Comment: 17 pages, three eps-figure

A Hopf laboratory for symmetric functions

An analysis of symmetric function theory is given from the perspective of the underlying Hopf and bi-algebraic structures. These are presented explicitly in terms of standard symmetric function operations. Particular attention is focussed on Laplace pairing, Sweedler cohomology for 1- and 2-cochains, and twisted products (Rota cliffordizations) induced by branching operators in the symmetric function context. The latter are shown to include the algebras of symmetric functions of orthogonal and symplectic type. A commentary on related issues in the combinatorial approach to quantum field theory is given.Comment: 29 pages, LaTeX, uses amsmat

Z_2-gradings of Clifford algebras and multivector structures

Let Cl(V,g) be the real Clifford algebra associated to the real vector space V, endowed with a nondegenerate metric g. In this paper, we study the class of Z_2-gradings of Cl(V,g) which are somehow compatible with the multivector structure of the Grassmann algebra over V. A complete characterization for such Z_2-gradings is obtained by classifying all the even subalgebras coming from them. An expression relating such subalgebras to the usual even part of Cl(V,g) is also obtained. Finally, we employ this framework to define spinor spaces, and to parametrize all the possible signature changes on Cl(V,g) by Z_2-gradings of this algebra.Comment: 10 pages, LaTeX; v2 accepted for publication in J. Phys.

On the Decomposition of Clifford Algebras of Arbitrary Bilinear Form

Clifford algebras are naturally associated with quadratic forms. These algebras are Z_2-graded by construction. However, only a Z_n-gradation induced by a choice of a basis, or even better, by a Chevalley vector space isomorphism Cl(V) \bigwedge V and an ordering, guarantees a multi-vector decomposition into scalars, vectors, tensors, and so on, mandatory in physics. We show that the Chevalley isomorphism theorem cannot be generalized to algebras if the Z_n-grading or other structures are added, e.g., a linear form. We work with pairs consisting of a Clifford algebra and a linear form or a Z_n-grading which we now call 'Clifford algebras of multi-vectors' or 'quantum Clifford algebras'. It turns out, that in this sense, all multi-vector Clifford algebras of the same quadratic but different bilinear forms are non-isomorphic. The usefulness of such algebras in quantum field theory and superconductivity was shown elsewhere. Allowing for arbitrary bilinear forms however spoils their diagonalizability which has a considerable effect on the tensor decomposition of the Clifford algebras governed by the periodicity theorems, including the Atiyah-Bott-Shapiro mod 8 periodicity. We consider real algebras Cl_{p,q} which can be decomposed in the symmetric case into a tensor product Cl_{p-1,q-1} \otimes Cl_{1,1}. The general case used in quantum field theory lacks this feature. Theories with non-symmetric bilinear forms are however needed in the analysis of multi-particle states in interacting theories. A connection to q-deformed structures through nontrivial vacuum states in quantum theories is outlined.Comment: 25 pages, 1 figure, LaTeX, {Paper presented at the 5th International Conference on Clifford Algebras and their Applications in Mathematical Physics, Ixtapa, Mexico, June 27 - July 4, 199

Off shell behaviour of the in medium nucleon-nucleon cross section

The properties of nucleon-nucleon scattering inside dense nuclear matter are investigated. We use the relativistic Brueckner-Hartree-Fock model to determine on-shell and half off-shell in-medium transition amplitudes and cross sections. At finite densities the on-shell cross sections are generally suppressed. This reduction is, however, less pronounced than found in previous works. In the case that the outgoing momenta are allowed to be off energy shell the amplitudes show a strong variation with momentum. This description allows to determine in-medium cross sections beyond the quasi-particle approximation accounting thereby for the finite width which nucleons acquire in the dense nuclear medium. For reasonable choices of the in-medium nuclear spectral width, i.e. $\Gamma\leq 40$ MeV, the resulting total cross sections are, however, reduced by not more than about 25% compared to the on-shell values. Off-shell effect are generally more pronounced at large nuclear matter densities.Comment: 31 pages Revtex, 12 figures, typos corrected, to appear in Phys. Rev.

Quantum field theory and Hopf algebra cohomology

We exhibit a Hopf superalgebra structure of the algebra of field operators of quantum field theory (QFT) with the normal product. Based on this we construct the operator product and the time-ordered product as a twist deformation in the sense of Drinfeld. Our approach yields formulas for (perturbative) products and expectation values that allow for a significant enhancement in computational efficiency as compared to traditional methods. Employing Hopf algebra cohomology sheds new light on the structure of QFT and allows the extension to interacting (not necessarily perturbative) QFT. We give a reconstruction theorem for time-ordered products in the spirit of Streater and Wightman and recover the distinction between free and interacting theory from a property of the underlying cocycle. We also demonstrate how non-trivial vacua are described in our approach solving a problem in quantum chemistry.Comment: 39 pages, no figures, LaTeX + AMS macros; title changed, minor corrections, references update

The structure of Green functions in quantum field theory with a general state

In quantum field theory, the Green function is usually calculated as the expectation value of the time-ordered product of fields over the vacuum. In some cases, especially in degenerate systems, expectation values over general states are required. The corresponding Green functions are essentially more complex than in the vacuum, because they cannot be written in terms of standard Feynman diagrams. Here, a method is proposed to determine the structure of these Green functions and to derive nonperturbative equations for them. The main idea is to transform the cumulants describing correlations into interaction terms.Comment: 13 pages, 6 figure

HtrA1 Mediated Intracellular Effects on Tubulin Using a Polarized RPE Disease Model

Age-related macular degeneration (AMD) is the leading cause of irreversible vision loss. The protein HtrA1 is enriched in retinal pigment epithelial (RPE) cells isolated from AMD patients and in drusen deposits. However, it is poorly understood how increased levels of HtrA1 affect the physiological function of the RPE at the intracellular level. Here, we developed hfRPE (human fetal retinal pigment epithelial) cell culture model where cells fully differentiated into a polarized functional monolayer. In this model, we fine-tuned the cellular levels of HtrA1 by targeted overexpression. Our data show that HtrA1 enzymatic activity leads to intracellular degradation of tubulin with a corresponding reduction in the number of microtubules, and consequently to an altered mechanical cell phenotype. HtrA1 overexpression further leads to impaired apical processes and decreased phagocytosis, an essential function for photoreceptor survival. These cellular alterations correlate with the AMD phenotype and thus highlight HtrA1 as an intracellular target for therapeutic interventions towards AMD treatment

Long-term outcome of patients with newly diagnosed chronic myeloid leukemia: a randomized comparison of stem cell transplantation with drug treatment.

Tyrosine kinase inhibitors represent today's treatment of choice in chronic myeloid leukemia (CML). Allogeneic hematopoietic stem cell transplantation (HSCT) is regarded as salvage therapy. This prospective randomized CML-study IIIA recruited 669 patients with newly diagnosed CML between July 1997 and January 2004 from 143 centers. Of these, 427 patients were considered eligible for HSCT and were randomized by availability of a matched family donor between primary HSCT (group A; N=166 patients) and best available drug treatment (group B; N=261). Primary end point was long-term survival. Survival probabilities were not different between groups A and B (10-year survival: 0.76 (95% confidence interval (CI): 0.69-0.82) vs 0.69 (95% CI: 0.61-0.76)), but influenced by disease and transplant risk. Patients with a low transplant risk showed superior survival compared with patients with high- (P<0.001) and non-high-risk disease (P=0.047) in group B; after entering blast crisis, survival was not different with or without HSCT. Significantly more patients in group A were in molecular remission (56% vs 39%; P=0.005) and free of drug treatment (56% vs 6%; P<0.001). Differences in symptoms and Karnofsky score were not significant. In the era of tyrosine kinase inhibitors, HSCT remains a valid option when both disease and transplant risk are considered