Analysis of the semileptonic (B_c -> B_u* l+ l-) decay from QCD sum rules

We analyze the semileptonic (B_c -> B_u* l+ l-) decay in the frame work of the Standard Model. We calculate the (B_c) to (B_u*) transition form factors in QCD sum rules. Analytical expressions for the spectral densities and gluon condensates are presented. The branching ratio of the (B_c -> B_u* l+ l-) decay is calculated, and it is obtained that this decay can be detectable at forthcoming LHC machines.Comment: 17 pages, no figures, LaTeX formatte

One-step generation of high-quality squeezed and EPR states in cavity QED

We show how to generate bilinear (quadratic) Hamiltonians in cavity quantum electrodynamics (QED) through the interaction of a single driven three-level atom with two (one) cavity modes. With this scheme it is possible to generate one-mode mesoscopic squeezed superpositions, two-mode entanglements, and two-mode squeezed vacuum states (such the original EPR state), without the need for Ramsey zones and external parametric amplification. The degree of squeezing achieved is up to 99% with currently feasible experimental parameters and the errors due to dissipative mechanisms become practically negligible

Investigation of a Protein Complex Network

The budding yeast {\it Saccharomyces cerevisiae} is the first eukaryote whose genome has been completely sequenced. It is also the first eukaryotic cell whose proteome (the set of all proteins) and interactome (the network of all mutual interactions between proteins) has been analyzed. In this paper we study the structure of the yeast protein complex network in which weighted edges between complexes represent the number of shared proteins. It is found that the network of protein complexes is a small world network with scale free behavior for many of its distributions. However we find that there are no strong correlations between the weights and degrees of neighboring complexes. To reveal non-random features of the network we also compare it with a null model in which the complexes randomly select their proteins. Finally we propose a simple evolutionary model based on duplication and divergence of proteins.Comment: 19 pages, 9 figures, 1 table, to appear in Euro. Phys. J.

An endeavor for a multidisciplinary case study : discussion on immigration and adaptation from the perspective of Human Sciences : Part 1

application/pdfdepartmental bulletin pape

John J. Bulow, Jr

31-1ClaimsReport : Claim of of J. Bulow, jr. [585] Creek and Seminole wars of 1836.1850-10

Measurement of the LT-asymmetry in \pi^0 electroproduction at the energy of the \Delta (1232) resonance

The reaction p(e,e'p)pi^0 has been studied at Q^2=0.2 (GeV/c)^2 in the region of W=1232 MeV. From measurements left and right of q, cross section asymmetries \rho_LT have been obtained in forward kinematics \rho_LT(\theta_\pi^0=20deg) = (-11.68 +/- 2.36_stat +/- 2.36_sys)$ and backward kinematics \rho_LT(\theta_\pi^0=160deg) =(12.18 +/- 0.27_stat +/- 0.82_sys). Multipole ratios \Re(S_1+^* M_1+)/|M_1+|^2 and \Re(S_0+^* M_1+)/|M_1+|^2 were determined in the framework of the MAID2003 model. The results are in agreement with older data. The unusally strong negative \Re(S_0+^* M_1+)/|M_1+|^2 required to bring also the result of Kalleicher et al. in accordance with the rest of the data is almost excluded.Comment: 7 pages, 7 figures, 4 tables. Changed content. Accepted for publication in EPJ

maritima

Triglochin maritima Linnaeusseaside arrowgrass;shore arrowgrass;common bog arrowgrass;arrowgrasstroscart maritimemaritimaabandonned channel of Cottonwood Creek south of 4080 So. Between 9th and 11th East.Pasture in an abandone channel. Moist, grazed area.4300 fee

pentandra

Tamarix pentandra PallAmur TamarixAmus TamarixGwen WalkerDeciduous shrub with extremely fine texture. Specimen collected from the Ornamental Block - Sec. 6A, Row 23, Plant 30, Horticulture Station, Brooks, Alberta. Height - 6 ft. Not hardy. Knowles says ""Good specimens are rare in Alta."