2,906 research outputs found
A precise new KLOE measurement of with ISR events and determination of contribution to for GeV
The KLOE experiment at the DANE -factory has performed a new
precise measurement of the pion form factor using Initial State Radiation
events, with photons emitted at small polar angle. Results based on an
integrated luminosity of 240 pb and extraction of the
contribution to in the mass range GeV are
presented. The new value of has smaller (30%) statistical and
systematic error and is consistent with the KLOE published value (confirming
the current disagreement between the standard model prediction for and
the measured value).Comment: 5 pages, proceedings for the CIPANP 2009 conferenc
Form factor in K+ --> pi+ pi0 gamma: interference versus direct emission
We analyze the effect of a form factor in the magnetic contribution to K+ -->
pi+ pi0 gamma. We emphasize how this can show up experimentally: in particular
we try to explore the difference between a possible interference contribution
and a form factor in the magnetic part. The form factor used for K+ --> pi+ pi0
gamma is analogous to the one for KL --> pi+ pi- gamma, experimentally well
established.Comment: 9 pages revtex, 10 eps figures; improved presentation of theoretical
and experimental status; refs. adde
Vector meson decays from the Extended Chiral Quark Model
We derive the the effective lagrangian that describes the interactions among
vector, axial-vector mesons and pseudoscalars starting from the extended chiral
quark model (ECQM). The results for the low-energy constants of this effective
lagrangian have a parametric resemblance with existing predictions based on the
Nambu-Jona-Lasinio model (except for some overall signs that we correct), but
are numerically different. Therefore a precise measurement of these decay
constants can shed some light on the way chiral symmetry breaking is modelled
in QCD. Although most of the constants are poorly measured, comparison with
phenomenology allows us to determine one of the parameters of the ECQM that
could not be fully determined in previous analyses.Comment: 7 pages, revtex
Precision Measurement of KS Meson Lifetime with the KLOE detector
Using a large sample of pure, slow, short lived K0 mesons collected with KLOE
detector at DaFne, we have measured the KS lifetime. From a fit to the proper
time distribution we find tau = (89.562 +- 0.029_stat +- 0.043_syst) ps. This
is the most precise measurement today in good agreement with the world average
derived from previous measurements. We observe no dependence of the lifetime on
the direction of the Ks.Comment: 5 pages, 7 figure
Study of isospin violating excitation in
We study the reaction in the vicinity of mass
region. The isospin-violating excitation is accounted for by two major
mechanisms. One is electromagnetic (EM) transition and the other is strong
isospin violations. For the latter, we consider contributions from the
intermediate hadronic meson loops and - mixing as the major
mechanisms via the and s-channel transitions, respectively. By fitting the
recent KLOE data, we succeed in constraining the model parameters and
extracting the branching ratio. It shows that the
branching ratio is sensitive to the excitation line shape and background
contributions. Some crucial insights into the correlation between isospin
violation and Okubo-Zweig-Iizuka (OZI) rule evading transitions are also
learned.Comment: Revised version to appear in J. Phys.
Reanalysis of pion pion phase shifts from K -> pi pi decays
We re-investigate the impact of isospin violation for extracting the s-wave
pion pion scattering phase shift difference delta_0(M_K) - delta_2(M_K) from K
-> pi pi decays. Compared to our previous analysis in 2003, more precise
experimental data and improved knowledge of low-energy constants are used. In
addition, we employ a more robust data-driven method to obtain the phase shift
difference delta_0(M_K) - delta_2(M_K) = (52.5 \pm 0.8_{exp} \pm 2.8_{theor})
degrees.Comment: 8 page
Comparative analysis of the SOL plasma in DEMO using EDGE2D/EIRENE and TECXY codes
In this contribution a benchmark of the 2D edge codes TECXY and EDGE2D-EIRENE is presented. A conventional DEMO scenario is considered by assuming a simplified geometry, with the target plates perpendicular to the separatrix, and a pure Deuterium plasma. Despite the different models adopted in the two codes, mainly related to the description of the neutral dynamics and to the different boundary conditions, the results show a good match both in terms of power load profiles on the outer target and predicted trends for global quantities. A scan in density and in diffusion coefficients is performed in order to identify the characteristic conditions and the different regimes of the SOL. Comparable values and similar dependency of the global quantities as a function of the power decay length is also observed. Keywords: EDGE2D, EIRENE, TECXY, DEMO, Diverto
The effect of estrogen and tamoxifen on hepatocyte proliferation in Vivo and in Vitro
We have previously shown that changes in estrogen‐hepatocyte interaction occur during liver regeneration. Following 70% hepatectomy, estrogen levels in the blood were elevated, the number of estrogen receptors in the liver was increased and there was an active translocation of estrogen receptors from the cytosol to the nucleus. The injection of tamoxifen, an estrogen antagonist, inhibits hepatocyte proliferation following partial hepatectomy. The administration of 1 μg tamoxifen per gm body weight at zero time or 6 hr after the operation resulted in a significant inhibition both of DNA synthesis and of the number of cells in mitosis. Injections of tamoxifen 12 hr or later after the operation had no effect. Concomitant injections of equimolar amounts of estrogen abolished the inhibition by tamoxifen. The effects of estrogen and tamoxifen were also tested on hepatocytes in primary culture. Estrogens in the presence of 5% normal rat serum stimulated hepatocyte DNA synthesis as determined by [3H]thymidine incorporation and the labeling index, whereas epidermal growth factor‐induced DNA synthesis in the absence of normal rat serum was strongly inhibited. Tamoxifen, in contrast, inhibited DNA synthesis of hepatocytes in the presence of 5% normal rat serum and reversed the stimulatory effect of estrogen in the same system. Attempts to elucidate the mechanism of tamoxifen inhibition in vitro indicated that one effect of tamoxifen is to prevent the amiloride‐sensitive Na+ influx necessary to initiate hepatocyte proliferation. Copyright © 1989 American Association for the Study of Liver Disease
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