51 research outputs found

    About one long-range contribution to K+ -> pi+ l+ l- decays

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    We investigate the mechanism of K+ -> pi+ l+ l- (l= e, mu) decays in which a virtual photon is emitted either from the incoming K+ or the outgoing pi+. We point out some inconsistencies with and between two previous calculations, discuss the possible experimental inputs, and estimate the branching fractions. This mechanism alone fails to explain the existing experimental data by more than one order-of-magnitude. But it may show itself by its interference with the leading long-range mechanism dominated by the a_1^+ and rho^0 mesons.Comment: 12 pages, RevTeX, epsf.sty, 2 embedded figure

    Running mass of the rho0 meson's implication for the dilepton mass spectrum and the mu+mu-/e+e- branching ratio in the K+ --> pi+l+l- decays

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    We make an attempt to resolve the discrepancy of the observed e+e- mass spectrum in the K+ --> pi+e+e- decay with that predicted by meson dominance. To this end we investigate the properties of the rho0 propagator. We use dispersion relations to evaluate the running mass squared m_rho^2(t) of the rho0 resonance without adjustable parameters. To improve the convergence of the dispersion integral, the momentum dependence of strong vertices is taken from the flux-tube-breaking model of Kokoski and Isgur. The obtained behavior of m_rho^2(t) at small momentum squared t makes the K+ --> pi+e+e- form factor rise faster with increasing tt than in the original meson-dominance calculation and more in agreement with the published data. As a consequence, the meson-dominance prediction of the mu+mu-/e+e- branching ratio changes slightly, from 0.224 to 0.236. We do not see any possibility to accommodate into the meson-dominance approach an even steeper e+e- spectrum, indicated by the preliminary data of the E865 collaboration at BNL AGS.Comment: 13 pages, RevTeX, epsf.sty, 4 embedded figure

    Two Photon Contribution to Polarization in K+→π+ÎŒ+Ό−K^+ \rightarrow \pi^+ \mu^+ \mu^-

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    Short distance physics involving virtual top and charm quarks contributes to ÎŒ+\mu^+ (and Ό−\mu^-) polarization in the decay K+→π+ÎŒ+Ό−K^+ \rightarrow \pi^+ \mu^+ \mu^-. Measurement of the parity violating asymmetry (ΓR−ΓL)/(ΓR+ΓL)(\Gamma_R - \Gamma_L)/(\Gamma_R + \Gamma_L), where ΓR\Gamma_R and ΓL\Gamma_L are the rates to produce right and left-handed ÎŒ+\mu^+, may provide valuable information on the unitarity triangle. The parity violating asymmetry also gets a contribution from Feynman diagrams with two photon intermediate states. We estimate this two photon contribution to the asymmetry and discuss briefly the two photon contribution to time reversal odd asymmetries that involve both the ÎŒ+\mu^+ and Ό−\mu^- polarizations.Comment: (19 pages, 5 figures available on request. Uses phyzzx), CALT-68-1798, UCSD/PTH 92-2

    A new measurement of the properties of the rare decay K -> pi+ e+ e-

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    A large low-background sample of events (10300) has been collected for the rare decay of kaons in flight K+ -> pi+ e+ e- by experiment E865 at the Brookhaven AGS. The decay products were accepted by a broad band high-resolution charged particle spectrometer with particle identification. The branching ratio (2.94 +- 0.05(stat.) +- 0.13(syst.) +- 0.05(model))*10**{-7} was determined normalizing to events from the decay chain K+ -> pi+ pi0; pi0 -> e+ e- gamma. From the analysis of the decay distributions the vector nature of this decay is firmly established now, and limits on scalar and tensor contributions are deduced. From the (e+ e-) invariant mass distribution the decay form factor f(z)=f0(1+ delta*z) (z=M(ee)**2/m(K)**2) is determined with delta=2.14 +- 0.13 +- 0.15. Chiral QCD perturbation theory predictions for the form factor are also tested, and terms beyond leading order O(p**4) are found to be important.Comment: 4 pages, 5 figure

    Weak Decays Beyond Leading Logarithms

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    We review the present status of QCD corrections to weak decays beyond the leading logarithmic approximation including particle-antiparticle mixing and rare and CP violating decays. After presenting the basic formalism for these calculations we discuss in detail the effective hamiltonians for all decays for which the next-to-leading corrections are known. Subsequently, we present the phenomenological implications of these calculations. In particular we update the values of various parameters and we incorporate new information on m_t in view of the recent top quark discovery. One of the central issues in our review are the theoretical uncertainties related to renormalization scale ambiguities which are substantially reduced by including next-to-leading order corrections. The impact of this theoretical improvement on the determination of the Cabibbo-Kobayashi-Maskawa matrix is then illustrated in various cases.Comment: 229 pages, 32 PostScript figures (included); uses RevTeX, epsf.sty, rotate.sty, rmpbib.sty (included), times.sty (included; requires LaTeX 2e); complete PostScript version available at ftp://feynman.t30.physik.tu-muenchen.de/pub/preprints/tum-100-95.ps.gz or ftp://feynman.t30.physik.tu-muenchen.de/pub/preprints/tum-100-95.ps2.gz (scaled down and rotated version to print two pages on one sheet of paper

    A New Measurement of the Rare Decay K+→π+ÎŒ+Ό−K^+\to \pi^+ \mu^+ \mu^-

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    More than 400 K+→π+ÎŒ+Ό−K^{+}\to\pi^{+}\mu^+\mu^- events were observed in a rare K+K^+ decay experiment at the AGS. Normalized to the K+→π+π+π−K^{+}\to\pi^{+}\pi^+\pi^- decay, the branching ratio is determined to be (9.22±0.60(stat)±0.49(syst))×10−8(9.22 \pm 0.60 (stat) \pm 0.49 (syst))\times 10^{-8}. This branching ratio and the ΌΌ\mu\mu mass spectrum is in very good agreement with the measurement of the K+→π+e+e−K^{+}\to\pi^{+}e^+e^- decay, but deviates significantly from the previous measurement.Comment: 4 pages, 6 figures in 7 eps files. Paper to be submitted to Phys Rev Let

    Observation of the Decay K- -> pi- mu+ mu- and Measurements of the Branching Ratios for K+/- -> pi+/- mu+ mu-

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    Using data collected with the HyperCP (E871) spectrometer during the 1997 fixed-target run at Fermilab, we report the first observation of the decay K- -> pi- mu+ mu- and new measurements of the branching ratios for K+/- -> pi+/- mu+ mu- . By combining the branching ratios for the K+ and K- decays, we measure the ratio (K+/- -> pi+/- mu+ mu-)/(K+/- -> all) = (9.8 +/- 1.0 +/- 0.5)x10^(-8). The CP asymmetry between the K+ and K- decay modes = -0.02 +/- 0.11 +/- 0.04.Comment: 4 pages, 4 figures, submitted to PR

    Viral, bacterial, and fungal infections of the oral mucosa:Types, incidence, predisposing factors, diagnostic algorithms, and management

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    Centrosome-associated RNA in surf clam oocytes

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    Centrosomes are the major microtubule-organizing center in animal cells. They are composed of a pair of [9(3) + 0] centrioles surrounded by a relatively ill-defined pericentriolar matrix, provide the ciliary centriole–kinetosome (basal body) progenitor, and organize the assembly of microtubules into the mitotic spindle during cell division. Despite >100 years of microscopic observation and their obvious significance, our understanding of centrosome composition, dynamic organization, and mechanism of action is limited when compared with that of other cellular organelles. Centrosomes duplicate only once per cell cycle to ensure development of a normal bipolar spindle. The initial event in centrosome duplication is centriole replication, which is generative, semiconservative, and independent of the nucleus. Such observations led to the proposal that centrosomes contain their own complement of nucleic acids, possibly representative of an organellar genome comparable with those described for mitochondria and chloroplasts. The consensus in the field is that centrosomes lack DNA but may contain RNA. We isolated centrosomes from oocytes of the surf clam, Spisula solidissima, and purified from them a unique set of RNAs. We show here by biochemical means and subcellular in situ hybridization that the first transcript we analyzed is intimately associated with centrosomes. Sequence analysis reveals that this centrosome-associated RNA encodes a conserved RNA-directed polymerase domain. The hypothesis that centrosomes contain an intrinsic complement of specific RNAs suggests new opportunities to address the century-old problem of centrosome function, heredity, and evolution
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