51 research outputs found
About one long-range contribution to K+ -> pi+ l+ l- decays
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
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 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
Short distance physics involving virtual top and charm quarks contributes to
(and ) polarization in the decay . Measurement of the parity violating asymmetry , where and are the rates
to produce right and left-handed , 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 and
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-
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
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
More than 400 events were observed in a rare
decay experiment at the AGS. Normalized to the
decay, the branching ratio is determined to be
. This branching ratio
and the mass spectrum is in very good agreement with the measurement
of the 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-
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
Centrosome-associated RNA in surf clam oocytes
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 centrioleâkinetosome (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
- âŠ