Form Factors for Lambda_b -> Lambda Transitions in SCET

We present a systematic discussion of Lambda_b -> Lambda transition form factors in the framework of soft-collinear effective theory (SCET). The universal soft form factor, which enters the symmetry relations in the limit of large recoil energy, is calculated from a sum-rule analysis of a suitable SCET correlation function. The same method is applied to derive the leading corrections from hard-collinear gluon exchange at first order in the strong coupling constant. We present numerical estimates for form factors and form-factor ratios and their impact on decay observables in Lambda_b -> Lambda mu^+ mu^- decays.Comment: 2+29 pages, 9 figures. Corrections in Sections 3.2 and 4 and Appendix D.1. Conclusions do not change. Erratum to appear in PR

Proton mass effects in wide-angle Compton scattering

We investigate proton mass effects in the handbag approach to wide-angle Compton scattering. We find that theoretical uncertainties due to the proton mass are significant for photon energies presently studied at Jefferson Lab. With the proposed energy upgrade such uncertainties will be clearly reduced.Comment: 4 pages, uses revtex, 3 figure

Light-Cone Distribution Amplitudes for Heavy-Quark Hadrons

We construct parametrizations of light-cone distribution amplitudes (LCDAs) for B-mesons and Lambda_b-baryons that obey various theoretical constraints, and which are simple to use in factorization theorems relevant for phenomenological applications in heavy-flavour physics. In particular, we find the eigenfunctions of the Lange-Neubert renormalization kernel, which allow for a systematic implementation of renormalization-group evolution effects for both B-meson and \Lambda_b-baryon decays. We also present a new strategy to construct LCDA models from momentum-space projectors, which can be used to implement Wandzura-Wilczek--like relations, and which allow for a comparison with theoretical approaches that go beyond the collinear limit for the light-quark momenta in energetic heavy-hadron decays.Comment: 39 pages, 11 figure

Effectiveness of zinc supplementation on diarrhea and average daily gain in pre-weaned dairy calves: A double-blind, block-randomized, placebo-controlled clinical trial.

The objective of this clinical trial was to evaluate the effectiveness of zinc supplementation on diarrhea and average daily weight gain (ADG) in pre-weaned dairy calves. A total of 1,482 healthy Holstein heifer and bull calves from a large California dairy were enrolled at 24 to 48 hours of age until hutch exit at approximately 90 days of age. Calves were block-randomized by time to one of three treatments: 1) placebo, 2) zinc methionine (ZM), or 3) zinc sulfate (ZS) administered in milk once daily for 14 days. Serum total protein at enrollment and body weight at birth, treatment end, and hutch exit were measured. Fecal consistency was assessed daily for 28 days post-enrollment. For a random sample of 127 calves, serum zinc concentrations before and after treatment and a fecal antigen ELISA at diarrhea start and resolution for Escherichia coli K99, rotavirus, coronavirus, and Cryptosporidium parvum were performed. Linear regression showed that ZM-treated bull calves had 22 g increased ADG compared to placebo-treated bulls (P = 0.042). ZM-treated heifers had 9 g decreased ADG compared to placebo-treated heifers (P = 0.037), after adjusting for average birth weight. Sex-stratified models showed that high birth weight heifers treated with ZM gained more than placebo-treated heifers of the same birth weight, which suggests a dose-response effect rather than a true sex-specific effect of ZM on ADG. Cox regression showed that ZM and ZS-treated calves had a 14.7% (P = 0.015) and 13.9% (P = 0.022) reduced hazard of diarrhea, respectively, compared to placebo-treated calves. Calves supplemented for at least the first five days of diarrhea with ZM and ZS had a 21.4% (P = 0.027) and 13.0% (P = 0.040) increased hazard of cure from diarrhea, respectively, compared to placebo-treated calves. Logistic regression showed that the odds of microbiological cure at diarrhea resolution for rotavirus, C. parvum, or any single fecal pathogen was not different between treatment groups. Zinc supplementation delayed diarrhea and expedited diarrhea recovery in pre-weaned calves. Additionally, zinc improved weight gain differentially in bulls compared to heifers, indicating a research need for sex-specific dosing

Decays of J/ψJ/\psi and ψ′\psi^\prime into vector and pseudoscalar meson and the pseudoscalar glueball-qqˉq\bar{q} mixing

We introduce a parametrization scheme for $J/\psi(\psi^\prime)\to VP$ where the effects of SU(3) flavor symmetry breaking and doubly OZI-rule violation (DOZI) can be parametrized by certain parameters with explicit physical interpretations. This scheme can be used to clarify the glueball-$q\bar{q}$ mixing within the pseudoscalar mesons. We also include the contributions from the electromagnetic (EM) decays of $J/\psi$ and $\psi^\prime$ via $J/\psi(\psi^\prime)\to \gamma^*\to VP$. Via study of the isospin violated channels, such as $J/\psi(\psi^\prime)\to \rho\eta$, $\rho\eta^\prime$, $\omega\pi^0$ and $\phi\pi^0$, reasonable constraints on the EM decay contributions are obtained. With the up-to-date experimental data for $J/\psi(\psi^\prime)\to VP$, $J/\psi(\psi^\prime)\to \gamma P$ and $P\to \gamma\gamma$, etc, we arrive at a consistent description of the mentioned processes with a minimal set of parameters. As a consequence, we find that there exists an overall suppression of the $\psi^\prime\to 3g$ form factors, which sheds some light on the long-standing "$\rho\pi$ puzzle". By determining the glueball components inside the pseudoscalar $\eta$ and $\eta^\prime$ in three different glueball-$q\bar{q}$ mixing schemes, we deduce that the lowest pseudoscalar glueball, if exists, has rather small $q\bar{q}$ component, and it makes the $\eta(1405)$ a preferable candidate for $0^{-+}$ glueball.Comment: Revised version to appear on J. Phys. G; An error in the code was corrected. There's slight change to the numerical results, while the conclusion is intac

Partition Function Zeros of a Restricted Potts Model on Lattice Strips and Effects of Boundary Conditions

We calculate the partition function $Z(G,Q,v)$ of the $Q$-state Potts model exactly for strips of the square and triangular lattices of various widths $L_y$ and arbitrarily great lengths $L_x$, with a variety of boundary conditions, and with $Q$ and $v$ restricted to satisfy conditions corresponding to the ferromagnetic phase transition on the associated two-dimensional lattices. From these calculations, in the limit $L_x \to \infty$, we determine the continuous accumulation loci ${\cal B}$ of the partition function zeros in the $v$ and $Q$ planes. Strips of the honeycomb lattice are also considered. We discuss some general features of these loci.Comment: 12 pages, 12 figure

CELL-MEDIATED IMMUNE RESPONSE IN VITRO : III. THE REQUIREMENT FOR MACROPHAGES IN CYTOTOXIC REACTIONS AGAINST CELL-BOUND AND SUBCELLULAR ALLOANTIGENS

All efficient cell separation procedure and specific anti-macrophage serum were used to investigate the requirement of macrophages in the in vitro allograft response of mouse lymphoid cells. The efficiency of the macrophage-depletion procedure used and the undiminished capacity of the purified lymphocytes to respond were verified by also testing the antibody responses to sheep red cells (SRC) and dinitrophenylated polymeric flagellin (DNP POL) as well as the proliferative response to allogeneic cells. It was found that the generation of cytotoxic lymphocytes were diminished after macrophage depletion by surface adherence. The combination of anti-macrophage serum and column purification resulted in the total abolition of cytotoxic activity. The cell-mediated immune response was restored completely by addition of peritoneal macrophages, with as few as 1 macrophage to 600 lymphocytes permitting a significant restoration. Macrophages were not involved in the cytotoxic effector phase, but were essential in immune induction. A subcellular H-2 alloantigen preparation was only immunogenic in the presence of macrophages, indicating that a mere reduction in the size of the antigen from cell-bound alloantigens to membrane fragments was not the sole function of macrophages. The results suggest that macrophages collaborate with T cells in the initiation of an allograft response in vitro

Exclusive channels in semi-inclusive production of pions and kaons

We investigate the role of exclusive channels in semi-inclusive electroproduction of pions and kaons. Using the QCD factorization theorem for hard exclusive processes we evaluate the cross sections for exclusive pseudoscalar and vector meson production in terms of generalized parton distributions and meson distribution amplitudes. We investigate the uncertainties arising from the modeling of the nonperturbative input quantities. Combining these results with available experimental data, we compare the cross sections for exclusive channels to that obtained from quark fragmentation in semi-inclusive deep inelastic scattering. We find that rho^0 production is the only exclusive channel with significant contributions to semi-inclusive pion production at large z and moderate Q^2. The corresponding contribution to kaon production from the decay of exclusively produced phi and K^* is rather small.Comment: 33 pages, 18 figure

Study of B→K(∗)ℓ+ℓ−B\to K^{(*)} \ell^+\ell^- Decays in the Family Non-universal Z′Z' Models

In a combined investigation of the $B\to K^{(*)}\ell^+\ell^-$ decays, constraints on the related couplings in family non-universal $Z^{\prime}$ models are derived. We find that within the allowed parameter space, the recently observed forward-backward asymmetry in the $B\to K^*\ell^+\ell^-$ decay can be explained, by flipping the signs of the Wilson coefficients $C_9^{\rm eff}$ and $C_{10}$. With the obtained constraints, we also calculate the branching ratio of the $B_s\to\mu^+\mu^-$ decay. The upper bound of our prediction is near the upper bound given by CDF Collaboration recently.Comment: 19 pages, 4 figures, some errors corrected; Journal versio