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Operationalising and measuring language dominance
The paper offers a new way to measure language ability in bilinguals, based on measures of lexical richness. The validity of proposed approach is tested in a variety of ways
Effect of stress level on the high temperature deformation and fracture mechanisms of Ti-45Al-2Nb-2Mn-0.8 vol. pct TiB²: an 'In Situ' experimental study
The effect of the applied stress on the deformation and crack nucleation and propagation mechanisms of a gamma-TiAl intermetallic alloy (Ti-45Al-2Nb-2Mn (at. pct)-0.8 vol. pct TiB2) was examined by means of in situ tensile (constant strain rate) and tensile-creep (constant load) experiments performed at 973 K (700 °C) using a scanning electron microscope. Colony boundary cracking developed during the secondary stage in creep tests at 300 and 400 MPa and during the tertiary stage of the creep tests performed at higher stresses. Colony boundary cracking was also observed in the constant strain rate tensile test. Interlamellar ledges were only found during the tensile-creep tests at high stresses (sigma > 400 MPa) and during the constant strain rate tensile test. Quantitative measurements of the nature of the crack propagation path along secondary cracks and along the primary crack indicated that colony boundaries were preferential sites for crack propagation under all the conditions investigated. The frequency of interlamellar cracking increased with stress, but this fracture mechanism was always of secondary importance. Translamellar cracking was only observed along the primary crack.Funding from the Spanish Ministry of Science and Innovation through projects (MAT2009-14547-C02-01 and MAT2009-14547-C02-02) is acknowledged. The Madrid Regional Government partially supported this project through the ESTRUMAT grant (P2009/MAT-1585). CJB acknowledges the support from the Spanish Ministry of Education for his sabbatical stay in Madrid (SAB2009-0045).Publicad
Search for CP Violation in Charged D Meson Decays
We report results of a search for CP violation in the singly
Cabibbo-suppressed decays D+ -> K- K+ pi+, phi pi+, K*(892)0 K+, and pi- pi+
pi+ based on data from the charm hadroproduction experiment E791 at Fermilab.
We search for a difference in the D+ and D- decay rates for each of the final
states. No evidence for a difference is seen. The decay rate asymmetry
parameters A(CP), defined as the difference in the D+ and D- decay rates
divided by the sum of the decay rates, are measured to be: A(CP)(K K pi) =
-0.014 +/- 0.029, A(CP)(phi pi) = -0.028 +/- 0.036, A(CP)(K*(892) K) = -0.010
+/- 0.050, and A(CP)(pi pi pi) = -0.017 +/- 0.042.Comment: 13 pages, 5 figures, 1 table; Elsevier LaTe
Differential cross sections, charge production asymmetry, and spin-density matrix elements for D*(2010) produced in 500 GeV/c pi^- nucleon interactions
We report differential cross sections for the production of D*(2010) produced
in 500 GeV/c pi^- nucleon interactions from experiment E791 at Fermilab, as
functions of Feynman-x (x_F) and transverse momentum squared (p_T^2). We also
report the D* +/- charge asymmetry and spin-density matrix elements as
functions of these variables. Investigation of the spin-density matrix elements
shows no evidence of polarization. The average values of the spin alignment are
\eta= 0.01 +- 0.02 and -0.01 +- 0.02 for leading and non-leading particles,
respectively.Comment: LaTeX2e (elsart.cls). 13 pages, 6 figures (eps files). Submitted to
Physics Letters
Branching Fractions for D0 -> K+K- and D0 -> pi+pi-, and a Search for CP Violation in D0 Decays
Using the large hadroproduced charm sample collected in experiment E791 at
Fermilab, we have measured ratios of branching fractions for the two-body
singly-Cabibbo-suppressed charged decays of the D0:
(D0 -> KK)/(D0 -> Kpi) = 0.109 +- 0.003 +- 0.003,
(D0 -> pipi)/(D0 -> Kpi) = 0.040 +- 0.002 +- 0.003, and
(D0 -> KK)/(D0 -> pipi) = 2.75 +- 0.15 +- 0.16. We have looked for
differences in the decay rates of D0 and D0bar to the CP eigenstates K+K- and
pi+pi-, and have measured the CP asymmetry parameters
A_CP(K+K-) = -0.010 +- 0.049 +- 0.012 and
A_CP(pi+pi-) = -0.049 +- 0.078 +- 0.030, both consistent with zero.Comment: 10 Postscript pages, including 2 figures. Submitted to Phys. Lett.
Asymmetries between the production of D+ and D- mesons from 500 GeV/c pi- nucleon interactions as a function of xF and pt**2
We present asymmetries between the production of D+ and D- mesons in Fermilab
experiment E791 as a function of xF and pt**2. The data used here consist of
74,000 fully-reconstructed charmed mesons produced by a 500 GeV/c pi- beam on C
and Pt foils. The measurements are compared to results of models which predict
differences between the production of heavy-quark mesons that have a light
quark in common with the beam (leading particles) and those that do not
(non-leading particles). While the default models do not agree with our data,
we can reach agreement with one of them, PYTHIA, by making a limited number of
changes to parameters used
Search for Rare and Forbidden Dilepton Decays of the D+, Ds, and D0 Charmed Mesons
We report the results of a search for flavor-changing neutral current,
lepton-flavor violating, and lepton-number violating decays of D+, Ds, and D0
mesons (and their antiparticles) into modes containing muons and electrons.
Using data from Fermilab charm hadroproduction experiment E791, we examine the
pi,l,l and K,l,l decay modes of D+ and Ds and the l+l- decay modes of D0. No
evidence for any of these decays is found. Therefore, we present
branching-fraction upper limits at 90% confidence level for the 24 decay modes
examined. Eight of these modes have no previously reported limits, and fourteen
are reported with significant improvements over previously published results.Comment: 12 pages, 3 figures, LaTeX, elsart.cls, epsf.sty, amsmath.sty
Submitted to Physics Letters
Measurement of the form-factor ratios for D+ --> K* l nu
The form factor ratios rv=V(0)/A1(0), r2=A2(0)/A1(0) and r3=A3(0)/A1(0) in
the decay D+ --> K* l nu, K* -->K-pi+ have been measured using data from charm
hadroproduction experiment E791 at Fermilab. From 3034 (595) signal
(background) events in the muon channel, we obtain rv=1.84+-0.11+-0.09,
r2=0.75+-0.08+-0.09 and, as a first measurement of r3, we find 0.04+-0.33
+-0.29. The values of the form factor ratios rv and r2 measured for the muon
channel are combined with the values of rv and r2 that we have measured in the
electron channel. The combined E791 results for the muon and electron channels
are rv=1.87+-0.08+-0.07 and r2=0.73+-0.06+-0.08.Comment: 9 pages + 3 figures ; submitted to PL
Mass Splitting and Production of and Measured in N Interactions
From a sample of decaying to the
final state, we have observed, in the hadroproduction experiment E791 at
Fermilab, and through
their decays to . The mass difference ) is measured to be ; for
, we find .
The rate of production from decays of the triplet is
(22\pm 2\pm 3) {%} of the total production assuming equal rate
of production from all three, as measured for and .
We do not observe a statistically significant baryon-antibaryon
production asymmetry. The and spectra of from
decays are observed to be similar to those for all 's
produced.Comment: 15 pages, uuencoded postscript 3 figures uuencoded, tar-compressed
fil
The SPOC domain is a phosphoserine binding module that bridges transcription machinery with co- and post-transcriptional regulators
The heptad repeats of the C-terminal domain (CTD) of RNA polymerase II (Pol II) are extensively modified throughout the transcription cycle. The CTD coordinates RNA synthesis and processing by recruiting transcription regulators as well as RNA capping, splicing and 3'end processing factors. The SPOC domain of PHF3 was recently identified as a CTD reader domain specifically binding to phosphorylated serine-2 residues in adjacent CTD repeats. Here, we establish the SPOC domains of the human proteins DIDO, SHARP (also known as SPEN) and RBM15 as phosphoserine binding modules that can act as CTD readers but also recognize other phosphorylated binding partners. We report the crystal structure of SHARP SPOC in complex with CTD and identify the molecular determinants for its specific binding to phosphorylated serine-5. PHF3 and DIDO SPOC domains preferentially interact with the Pol II elongation complex, while RBM15 and SHARP SPOC domains engage with writers and readers of mA, the most abundant RNA modification. RBM15 positively regulates mA levels and mRNA stability in a SPOC-dependent manner, while SHARP SPOC is essential for its localization to inactive X-chromosomes. Our findings suggest that the SPOC domain is a major interface between the transcription machinery and regulators of transcription and co-transcriptional processes
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