801 research outputs found
Probing the Nature of Short Swift Bursts via Deep INTEGRAL Monitoring of GRB 050925
We present results from Swift, XMM-Newton, and deep INTEGRAL monitoring in
the region of GRB 050925. This short Swift burst is a candidate for a newly
discovered soft gamma-ray repeater (SGR) with the following observational burst
properties: 1) galactic plane (b=-0.1 deg) localization, 2) 150 msec duration,
and 3) a blackbody rather than a simple power-law spectral shape (with a
significance level of 97%). We found two possible X-ray counterparts of GRB
050925 by comparing the X-ray images from Swift XRT and XMM-Newton. Both X-ray
sources show the transient behavior with a power-law decay index shallower than
-1. We found no hard X-ray emission nor any additional burst from the location
of GRB 050925 in ~5 Ms of INTEGRAL data. We discuss about the three BATSE short
bursts which might be associated with GRB 050925, based on their location and
the duration. Assuming GRB 050925 is associated with the H II regions (W 58) at
the galactic longitude of l=70 deg, we also discuss the source frame properties
of GRB 050925.Comment: 13 pages, 13 figures, accepted for publication in ASR special issue
on Neutron Stars and Gamma Ray Bursts, full resolution of Fig 5 is available
at
http://asd.gsfc.nasa.gov/Takanori.Sakamoto/GRB050925/integral_ibis_images.ep
Fork pausing allows centromere DNA loop formation and kinetochore assembly
De novo kinetochore assembly, but not template-directed assembly, is dependent on COMA, the kinetochore complex engaged in cohesin recruitment. The slowing of replication fork progression by treatment with phleomycin (PHL), hydroxyurea, or deletion of the replication fork protection protein Csm3 can activate de novo kinetochore assembly in COMA mutants. Centromere DNA looping at the site of de novo kinetochore assembly can be detected shortly after exposure to PHL. Using simulations to explore the thermodynamics of DNA loops, we propose that loop formation is disfavored during bidirectional replication fork migration. One function of replication fork stalling upon encounters with DNA damage or other blockades may be to allow time for thermal fluctuations of the DNA chain to explore numerous configurations. Biasing thermodynamics provides a mechanism to facilitate macromolecular assembly, DNA repair, and other nucleic acid transactions at the replication fork. These loop configurations are essential for sister centromere separation and kinetochore assembly in the absence of the COMA complex
Stu2 uses a 15-nm parallel coiled coil for kinetochore localization and concomitant regulation of the mitotic spindle
XMAP215/Dis1 family proteins are potent microtubule polymerases, critical for mitotic spindle structure and dynamics. While microtubule polymerase activity is driven by an N-terminal tumor overexpressed gene (TOG) domain array, proper cellular localization is a requisite for full activity and is mediated by a C-terminal domain. Structural insight into the C-terminal domain's architecture and localization mechanism remain outstanding. We present the crystal structure of the Saccharomyces cerevisiae Stu2 C-terminal domain, revealing a 15-nm parallel homodimeric coiled coil. The parallel architecture of the coiled coil has mechanistic implications for the arrangement of the homodimer's N-terminal TOG domains during microtubule polymerization. The coiled coil has two spatially distinct conserved regions: CRI and CRII. Mutations in CRI and CRII perturb the distribution and localization of Stu2 along the mitotic spindle and yield defects in spindle morphology including increased frequencies of mispositioned and fragmented spindles. Collectively, these data highlight roles for the Stu2 dimerization domain as a scaffold for factor binding that optimally positions Stu2 on the mitotic spindle to promote proper spindle structure and dynamics
Heavy quarkonium 2S states in light-front quark model
We study the charmonium 2S states and , and the bottomonium
2S states and , using the light-front quark model and the
2S state wave function of harmonic oscillator as the approximation of the 2S
quarkonium wave function. The decay constants, transition form factors and
masses of these mesons are calculated and compared with experimental data.
Predictions of quantities such as Br are made. The
2S wave function may help us learn more about the structure of these heavy
quarkonia.Comment: 5 latex pages, final version for journal publicatio
Effective Lagrangian Approach to the Theory of Eta Photoproduction in the Region
We investigate eta photoproduction in the resonance region
within the effective Lagrangian approach (ELA), wherein leading contributions
to the amplitude at the tree level are taken into account. These include the
nucleon Born terms and the leading -channel vector meson exchanges as the
non-resonant pieces. In addition, we consider five resonance contributions in
the - and - channel; besides the dominant , these are:
and . The amplitudes for the
and the photoproduction near threshold have significant
differences, even as they share common contributions, such as those of the
nucleon Born terms. Among these differences, the contribution to the
photoproduction of the -channel excitation of the is the most
significant. We find the off-shell properties of the spin-3/2 resonances to be
important in determining the background contributions. Fitting our effective
amplitude to the available data base allows us to extract the quantity
, characteristic of the
photoexcitation of the resonance and its decay into the
-nucleon channel, of interest to precise tests of hadron models. At the
photon point, we determine it to be from
the old data base, and from a
combination of old data base and new Bates data. We obtain the helicity
amplitude for to be from the old data base, and from the combination of the old data base and new Bates
data, compared with the results of the analysis of pion photoproduction
yielding , in the same units.Comment: 43 pages, RevTeX, 9 figures available upon request, to appear in
Phys. Rev.
Study of the B^0 Semileptonic Decay Spectrum at the Upsilon(4S) Resonance
We have made a first measurement of the lepton momentum spectrum in a sample
of events enriched in neutral B's through a partial reconstruction of B0 -->
D*- l+ nu. This spectrum, measured with 2.38 fb**-1 of data collected at the
Upsilon(4S) resonance by the CLEO II detector, is compared directly to the
inclusive lepton spectrum from all Upsilon(4S) events in the same data set.
These two spectra are consistent with having the same shape above 1.5 GeV/c.
From the two spectra and two other CLEO measurements, we obtain the B0 and B+
semileptonic branching fractions, b0 and b+, their ratio, and the production
ratio f+-/f00 of B+ and B0 pairs at the Upsilon(4S). We report b+/b0=0.950
(+0.117-0.080) +- 0.091, b0 = (10.78 +- 0.60 +- 0.69)%, and b+ = (10.25 +- 0.57
+- 0.65)%. b+/b0 is equivalent to the ratio of charged to neutral B lifetimes,
tau+/tau0.Comment: 14 page, postscript file also available at
http://w4.lns.cornell.edu/public/CLN
Observation of the Charmed Baryon Decays to , , and
We have observed two new decay modes of the charmed baryon into
and using data collected with the
CLEO II detector. We also present the first measurement of the branching
fraction for the previously observed decay mode . The branching fractions for these three modes relative to
are measured to be , , and , respectively.Comment: 12 page uuencoded postscript file, postscript file also available
through http://w4.lns.cornell.edu/public/CLN
Production and Decay of D_1(2420)^0 and D_2^*(2460)^0
We have investigated and final states and
observed the two established charmed mesons, the with mass
MeV/c and width MeV/c and
the with mass MeV/c and width
MeV/c. Properties of these final states, including
their decay angular distributions and spin-parity assignments, have been
studied. We identify these two mesons as the doublet predicted
by HQET. We also obtain constraints on {\footnotesize } as a function of the cosine of the relative phase of the two
amplitudes in the decay.Comment: 15 pages in REVTEX format. hardcopies with figures can be obtained by
sending mail to: [email protected]
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