284 research outputs found
On the alpha activity of natural tungsten isotopes
The indication for the alpha decay of 180-W with a half-life
T1/2=1.1+0.8-0.4(stat)+-0.3(syst)x10^18 yr has been observed for the first time
with the help of the super-low background 116-CdWO_4 crystal scintillators. In
conservative approach the lower limit on half-life of 180-W has been
established as T1/2>0.7x10^18 yr at 90% C.L. Besides, new T1/2 bounds were set
for alpha decay of 182-W, 183-W, 184-W and 186-W at the level of 10^20 yr.Comment: 16 pages, 8 figures, accepted in Phys. Rev.
Electroweak Radiative Corrections to Parity-Violating Electroexcitation of the
We analyze the degree to which parity-violating (PV) electroexcitation of the
resonance may be used to extract the weak neutral axial vector
transition form factors. We find that the axial vector electroweak radiative
corrections are large and theoretically uncertain, thereby modifying the
nominal interpretation of the PV asymmetry in terms of the weak neutral form
factors. We also show that, in contrast to the situation for elastic electron
scattering, the axial PV asymmetry does not vanish at the photon
point as a consequence of a new term entering the radiative corrections. We
argue that an experimental determination of these radiative corrections would
be of interest for hadron structure theory, possibly shedding light on the
violation of Hara's theorem in weak, radiative hyperon decays.Comment: RevTex, 76 page
Relativistic close coupling calculations for photoionization and recombination of Ne-like Fe XVII
Relativistic and channel coupling effects in photoionization and unified
electronic recombination of Fe XVII are demonstrated with an extensive 60-level
close coupling calculation using the Breit-Pauli R-matrix method.
Photoionization and (e + ion) recombination calculations are carried out for
the total and the level-specific cross sections, including the ground and
several hundred excited bound levels of Fe XVII (up to fine structure levels
with n = 10). The unified (e + ion) recombination calculations for (e + Fe
XVIII --> Fe XVII) include both the non-resonant and resonant recombination
(`radiative' and `dielectronic recombination' -- RR and DR). The low-energy and
the high energy cross sections are compared from: (i) a 3-level calculation
with 2s^2p^5 (^2P^o_{1/2,3/2}) and 2s2p^6 (^2S_{1/2}), and (ii) the first
60-level calculation with \Delta n > 0 coupled channels with spectroscopic
2s^2p^5, 2s2p^6, 2s^22p^4 3s, 3p, 3d, configurations, and a number of
correlation configurations. Strong channel coupling effects are demonstrated
throughout the energy ranges considered, in particular via giant
photoexcitation-of-core (PEC) resonances due to L-M shell dipole transition
arrays 2p^5 --> 2p^4 3s, 3d in Fe XIII that enhance effective cross sections by
orders of magnitude. Comparison is made with previous theoretical and
experimental works on photoionization and recombination that considered the
relatively small low-energy region (i), and the weaker \Delta n = 0 couplings.
While the 3-level results are inadequate, the present 60-level results should
provide reasonably complete and accurate datasets for both photoionization and
(e + ion) recombination of Fe~XVII in laboratory and astrophysical plasmas.Comment: 19 pages, 8 figures, Phys. Rev. A (submitted
Mutation of Ser172 in Yeast β Tubulin Induces Defects in Microtubule Dynamics and Cell Division
Ser172 of β tubulin is an important residue that is mutated in a human brain disease and phosphorylated by the cyclin-dependent kinase Cdk1 in mammalian cells. To examine the role of this residue, we used the yeast S. cerevisiae as a model and produced two different mutations (S172A and S172E) of the conserved Ser172 in the yeast β tubulin Tub2p. The two mutants showed impaired cell growth on benomyl-containing medium and at cold temperatures, altered microtubule (MT) dynamics, and altered nucleus positioning and segregation. When cytoplasmic MT effectors Dyn1p or Kar9p were deleted in S172A and S172E mutants, cells were viable but presented increased ploidy. Furthermore, the two β tubulin mutations exhibited synthetic lethal interactions with Bik1p, Bim1p or Kar3p, which are effectors of cytoplasmic and spindle MTs. In the absence of Mad2p-dependent spindle checkpoint, both mutations are deleterious. These findings show the importance of Ser172 for the correct function of both cytoplasmic and spindle MTs and for normal cell division
Observation of exclusive DVCS in polarized electron beam asymmetry measurements
We report the first results of the beam spin asymmetry measured in the
reaction e + p -> e + p + gamma at a beam energy of 4.25 GeV. A large asymmetry
with a sin(phi) modulation is observed, as predicted for the interference term
of Deeply Virtual Compton Scattering and the Bethe-Heitler process. The
amplitude of this modulation is alpha = 0.202 +/- 0.028. In leading-order and
leading-twist pQCD, the alpha is directly proportional to the imaginary part of
the DVCS amplitude.Comment: 6 pages, 5 figure
Quantum walks: a comprehensive review
Quantum walks, the quantum mechanical counterpart of classical random walks,
is an advanced tool for building quantum algorithms that has been recently
shown to constitute a universal model of quantum computation. Quantum walks is
now a solid field of research of quantum computation full of exciting open
problems for physicists, computer scientists, mathematicians and engineers.
In this paper we review theoretical advances on the foundations of both
discrete- and continuous-time quantum walks, together with the role that
randomness plays in quantum walks, the connections between the mathematical
models of coined discrete quantum walks and continuous quantum walks, the
quantumness of quantum walks, a summary of papers published on discrete quantum
walks and entanglement as well as a succinct review of experimental proposals
and realizations of discrete-time quantum walks. Furthermore, we have reviewed
several algorithms based on both discrete- and continuous-time quantum walks as
well as a most important result: the computational universality of both
continuous- and discrete- time quantum walks.Comment: Paper accepted for publication in Quantum Information Processing
Journa
A Bayesian analysis of pentaquark signals from CLAS data
We examine the results of two measurements by the CLAS collaboration, one of
which claimed evidence for a pentaquark, whilst the other found no
such evidence. The unique feature of these two experiments was that they were
performed with the same experimental setup. Using a Bayesian analysis we find
that the results of the two experiments are in fact compatible with each other,
but that the first measurement did not contain sufficient information to
determine unambiguously the existence of a . Further, we suggest a
means by which the existence of a new candidate particle can be tested in a
rigorous manner.Comment: 5 pages, 3 figure
eta-prime photoproduction on the proton for photon energies from 1.527 to 2.227 GeV
Differential cross sections for the reaction gamma p -> eta-prime p have been
measured with the CLAS spectrometer and a tagged photon beam with energies from
1.527 to 2.227 GeV. The results reported here possess much greater accuracy
than previous measurements. Analyses of these data indicate for the first time
the coupling of the etaprime N channel to both the S_11(1535) and P_11(1710)
resonances, known to couple strongly to the eta N channel in photoproduction on
the proton, and the importance of j=3/2 resonances in the process.Comment: 6 pages, 3 figure
Measurement of the Deuteron Structure Function F2 in the Resonance Region and Evaluation of Its Moments
Inclusive electron scattering off the deuteron has been measured to extract
the deuteron structure function F2 with the CEBAF Large Acceptance Spectrometer
(CLAS) at the Thomas Jefferson National Accelerator Facility. The measurement
covers the entire resonance region from the quasi-elastic peak up to the
invariant mass of the final-state hadronic system W~2.7 GeV with four-momentum
transfers Q2 from 0.4 to 6 (GeV/c)^2. These data are complementary to previous
measurements of the proton structure function F2 and cover a similar
two-dimensional region of Q2 and Bjorken variable x. Determination of the
deuteron F2 over a large x interval including the quasi-elastic peak as a
function of Q2, together with the other world data, permit a direct evaluation
of the structure function moments for the first time. By fitting the Q2
evolution of these moments with an OPE-based twist expansion we have obtained a
separation of the leading twist and higher twist terms. The observed Q2
behaviour of the higher twist contribution suggests a partial cancellation of
different higher twists entering into the expansion with opposite signs. This
cancellation, found also in the proton moments, is a manifestation of the
"duality" phenomenon in the F2 structure function
An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics
For a decade, The Cancer Genome Atlas (TCGA) program collected clinicopathologic annotation data along with multi-platform molecular profiles of more than 11,000 human tumors across 33 different cancer types. TCGA clinical data contain key features representing the democratized nature of the data collection process. To ensure proper use of this large clinical dataset associated with genomic features, we developed a standardized dataset named the TCGA Pan-Cancer Clinical Data Resource (TCGA-CDR), which includes four major clinical outcome endpoints. In addition to detailing major challenges and statistical limitations encountered during the effort of integrating the acquired clinical data, we present a summary that includes endpoint usage recommendations for each cancer type. These TCGA-CDR findings appear to be consistent with cancer genomics studies independent of the TCGA effort and provide opportunities for investigating cancer biology using clinical correlates at an unprecedented scale. Analysis of clinicopathologic annotations for over 11,000 cancer patients in the TCGA program leads to the generation of TCGA Clinical Data Resource, which provides recommendations of clinical outcome endpoint usage for 33 cancer types
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