53 research outputs found
Extracting Br(omega->pi^+ pi^-) from the Time-like Pion Form-factor
We extract the G-parity-violating branching ratio Br(omega->pi^+ pi^-) from
the effective rho-omega mixing matrix element Pi_{rho omega}(s), determined
from e^+e^- -> pi^+ pi^- data. The omega->pi^+ pi^- partial width can be
determined either from the time-like pion form factor or through the constraint
that the mixed physical propagator D_{rho omega}^{mu nu}(s) possesses no poles.
The two procedures are inequivalent in practice, and we show why the first is
preferred, to find finally Br(omega->pi^+ pi^-) = 1.9 +/- 0.3%.Comment: 12 pages (published version
J/Psi strong couplings to the vector mesons
We present a study of the cross sections J/Psi X --> D^(*) \bar D^(*) (X =
rho, Phi) based on the calculation of the effective tri- and four-linear
couplings
J/Psi (X) D^(*) \bar D^(*) within a constituent quark model. In particular,
the details of the calculation of the four-linear couplings J/Psi X D^(*)\bar
D^(*) are given. The results obtained have been used in a recent analysis of
J/Psi absorption by the hot hadron gas formed in peripheral heavy-ion
collisions at SPS energies.Comment: 12 pages, 3 figure
Time-of-arrival distributions from position-momentum and energy-time joint measurements
The position-momentum quasi-distribution obtained from an Arthurs and Kelly
joint measurement model is used to obtain indirectly an ``operational''
time-of-arrival (TOA) distribution following a quantization procedure proposed
by Kocha\'nski and W\'odkiewicz [Phys. Rev. A 60, 2689 (1999)]. This TOA
distribution is not time covariant. The procedure is generalized by using other
phase-space quasi-distributions, and sufficient conditions are provided for
time covariance that limit the possible phase-space quasi-distributions
essentially to the Wigner function, which, however, provides a non-positive TOA
quasi-distribution. These problems are remedied with a different quantization
procedure which, on the other hand, does not guarantee normalization. Finally
an Arthurs and Kelly measurement model for TOA and energy (valid also for
arbitrary conjugate variables when one of the variables is bounded from below)
is worked out. The marginal TOA distribution so obtained, a distorted version
of Kijowski's distribution, is time covariant, positive, and normalized
Open Issues on the Synthesis of Evolved Stellar Populations at Ultraviolet Wavelengths
In this paper we briefly review three topics that have motivated our (and
others') investigations in recent years within the context of evolutionary
population synthesis techniques. These are: The origin of the FUV up-turn in
elliptical galaxies, the age-metallicity degeneracy, and the study of the
mid-UV rest-frame spectra of distant red galaxies. We summarize some of our
results and present a very preliminary application of a UV grid of theoretical
spectra in the analysis of integrated properties of aged stellar populations.
At the end, we concisely suggest how these topics can be tackled once the World
Space Observatory enters into operation in the midst of this decade.Comment: 8 pages, 4 figures, accepted for publication in Astrophysics & Space
Science, UV Universe special issu
Cosmological parameters from SDSS and WMAP
We measure cosmological parameters using the three-dimensional power spectrum
P(k) from over 200,000 galaxies in the Sloan Digital Sky Survey (SDSS) in
combination with WMAP and other data. Our results are consistent with a
``vanilla'' flat adiabatic Lambda-CDM model without tilt (n=1), running tilt,
tensor modes or massive neutrinos. Adding SDSS information more than halves the
WMAP-only error bars on some parameters, tightening 1 sigma constraints on the
Hubble parameter from h~0.74+0.18-0.07 to h~0.70+0.04-0.03, on the matter
density from Omega_m~0.25+/-0.10 to Omega_m~0.30+/-0.04 (1 sigma) and on
neutrino masses from <11 eV to <0.6 eV (95%). SDSS helps even more when
dropping prior assumptions about curvature, neutrinos, tensor modes and the
equation of state. Our results are in substantial agreement with the joint
analysis of WMAP and the 2dF Galaxy Redshift Survey, which is an impressive
consistency check with independent redshift survey data and analysis
techniques. In this paper, we place particular emphasis on clarifying the
physical origin of the constraints, i.e., what we do and do not know when using
different data sets and prior assumptions. For instance, dropping the
assumption that space is perfectly flat, the WMAP-only constraint on the
measured age of the Universe tightens from t0~16.3+2.3-1.8 Gyr to
t0~14.1+1.0-0.9 Gyr by adding SDSS and SN Ia data. Including tensors, running
tilt, neutrino mass and equation of state in the list of free parameters, many
constraints are still quite weak, but future cosmological measurements from
SDSS and other sources should allow these to be substantially tightened.Comment: Minor revisions to match accepted PRD version. SDSS data and ppt
figures available at http://www.hep.upenn.edu/~max/sdsspars.htm
Horizontal Branch Stars: The Interplay between Observations and Theory, and Insights into the Formation of the Galaxy
We review HB stars in a broad astrophysical context, including both variable
and non-variable stars. A reassessment of the Oosterhoff dichotomy is
presented, which provides unprecedented detail regarding its origin and
systematics. We show that the Oosterhoff dichotomy and the distribution of
globular clusters (GCs) in the HB morphology-metallicity plane both exclude,
with high statistical significance, the possibility that the Galactic halo may
have formed from the accretion of dwarf galaxies resembling present-day Milky
Way satellites such as Fornax, Sagittarius, and the LMC. A rediscussion of the
second-parameter problem is presented. A technique is proposed to estimate the
HB types of extragalactic GCs on the basis of integrated far-UV photometry. The
relationship between the absolute V magnitude of the HB at the RR Lyrae level
and metallicity, as obtained on the basis of trigonometric parallax
measurements for the star RR Lyrae, is also revisited, giving a distance
modulus to the LMC of (m-M)_0 = 18.44+/-0.11. RR Lyrae period change rates are
studied. Finally, the conductive opacities used in evolutionary calculations of
low-mass stars are investigated. [ABRIDGED]Comment: 56 pages, 22 figures. Invited review, to appear in Astrophysics and
Space Scienc
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
The concentrations of high- and low-density-lipoprotein cholesterol and triglycerides are influenced by smoking, but it is unknown whether genetic associations with lipids may be modified by smoking. We conducted a multi-ancestry genome-wide gene–smoking interaction study in 133,805 individuals with follow-up in an additional 253,467 individuals. Combined meta-analyses identified 13 new loci associated with lipids, some of which were detected only because association differed by smoking status. Additionally, we demonstrate the importance of including diverse populations, particularly in studies of interactions with lifestyle factors, where genomic and lifestyle differences by ancestry may contribute to novel findings
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Many genetic loci affect circulating lipid levels, but it remains unknown whether lifestyle factors, such as physical activity, modify these genetic effects. To identify lipid loci interacting with physical activity, we performed genome-wide analyses of circulating HDL cholesterol, LDL cholesterol, and triglyceride levels in up to 120,979 individuals of European, African, Asian, Hispanic, and Brazilian ancestry, with follow-up of suggestive associations in an additional 131,012 individuals. We find four loci, in/near CLASP1, LHX1, SNTA1, and CNTNAP2, that are associated with circulating lipid levels through interaction with physical activity; higher levels of physical activity enhance the HDL cholesterol-increasing effects of the CLASP1, LHX1, and SNTA1 loci and attenuate the LDL cholesterol- increasing effect of the CNTNAP2 locus. The CLASP1, LHX1, and SNTA1 regions harbor genes linked to muscle function and lipid metabolism. Our results elucidate the role of physical activity interactions in the genetic contribution to blood lipid levels
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