7,095 research outputs found
Estimations of the Distances of Stellar Collapses in the Galaxy by Analyzing the Energy Spectrum of Neutrino Bursts
The neutrino telescopes of the present generation, depending on their
specific features, can reconstruct the neutrino spectra from a galactic burst.
Since the optical counterpart could be not available, it is desirable to have
at hand alternative methods to estimate the distance of the supernova explosion
using only the neutrino data. In this work we present preliminary results on
the method we are proposing to estimate the distance from a galactic supernova
based only on the spectral shape of the neutrino burst and assumptions on the
gravitational binding energy released an a typical supernova explosion due to
stellar collapses.Comment: Proceedings of the Second International Symposium on Strong
Electromagnetic Fields and Neutron Stars (SMFNS 2011) Instituto de
Cibern\'etica, Matem\'atica y F\'isica (ICIMAF) Sociedad Cubana de F\'isica
(SCF) Varadero, Cuba, 5-7 May 201
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High-resolution provenance of desert dust deposited on Mt. Elbrus, Caucasus in 2009–2012 using snow pit and firn core records
The first record of dust deposition events on
Mt. Elbrus, Caucasus Mountains derived from a snow pit
and a shallow firn core is presented for the 2009–2012 period. A combination of isotopic analysis, SEVIRI red-greenblue composite imagery, MODIS atmospheric optical depth
fields derived using the Deep Blue algorithm, air mass trajectories derived using the HYSPLIT model and analyses of
meteorological data enabled identification of dust source regions with high temporal (hours) and spatial (ca. 20–100 km)
resolution. Seventeen dust deposition events were detected;
fourteen occurred in March–June, one in February and two
in October. Four events originated in the Sahara, predominantly in northeastern Libya and eastern Algeria. Thirteen
events originated in the Middle East, in the Syrian Desert
and northern Mesopotamia, from a mixture of natural and
anthropogenic sources. Dust transportation from Sahara was
associated with vigorous Saharan depressions, strong surface
winds in the source region and mid-tropospheric southwesterly flow with daily winds speeds of 20–30 m s−1
at 700 hPa
level. Although these events were less frequent than those
originating in the Middle East, they resulted in higher dust
concentrations in snow. Dust transportation from the Middle
East was associated with weaker depressions forming over
the source region, high pressure centred over or extending towards the Caspian Sea and a weaker southerly or southeasterly flow towards the Caucasus Mountains with daily wind
speeds of 12–18 m s−1
at 700 hPa level. Higher concentrations of nitrates and ammonium characterised dust from the
Middle East deposited on Mt. Elbrus in 2009 indicating contribution of anthropogenic sources. The modal values of particle size distributions ranged between 1.98 µm and 4.16 µm.
Most samples were characterised by modal values of 2.0–
2.8 µm with an average of 2.6 µm and there was no signifi-
cant difference between dust from the Sahara and the Middle
East
Quantum Symmetries and Strong Haagerup Inequalities
In this paper, we consider families of operators in
a tracial C-probability space , whose joint
-distribution is invariant under free complexification and the action of
the hyperoctahedral quantum groups . We prove a strong
form of Haagerup's inequality for the non-self-adjoint operator algebra
generated by , which generalizes the
strong Haagerup inequalities for -free R-diagonal families obtained by
Kemp-Speicher \cite{KeSp}. As an application of our result, we show that
always has the metric approximation property (MAP). We also apply
our techniques to study the reduced C-algebra of the free unitary
quantum group . We show that the non-self-adjoint subalgebra generated by the matrix elements of the fundamental corepresentation of
has the MAP. Additionally, we prove a strong Haagerup inequality for
, which improves on the estimates given by Vergnioux's property
RD \cite{Ve}
Oral dosing for antenatal corticosteroids in the Rhesus macaque.
Antenatal corticosteroids (ACS) are standard of care for women at risk of preterm delivery, although choice of drug, dose or route have not been systematically evaluated. Further, ACS are infrequently used in low resource environments where most of the mortality from prematurity occurs. We report proof of principle experiments to test betamethasone-phosphate (Beta-P) or dexamethasone-phosphate (Dex-P) given orally in comparison to the clinical treatment with the intramuscular combination drug beta-phosphate plus beta-acetate in a Rhesus Macaque model. First, we performed pharmacokinetic studies in non-pregnant monkeys to compare blood levels of the steroids using oral dosing with Beta-P, Dex-P and an effective maternal intramuscular dose of the beta-acetate component of the clinical treatment. We then evaluated maternal and fetal blood steroid levels with limited fetal sampling under ultrasound guidance in pregnant macaques. We found that oral Beta is more slowly cleared from plasma than oral Dex. The blood levels of both drugs were lower in maternal plasma of pregnant than in non-pregnant macaques. Using the pharmacokinetic data, we treated groups of 6-8 pregnant monkeys with oral Beta-P, oral Dex-P, or the maternal intramuscular clinical treatment and saline controls and measured pressure-volume curves to assess corticosteroid effects on lung maturation at 5d. Oral Beta-P improved the pressure-volume curves similarly to the clinical treatment. Oral Dex-P gave more variable and nonsignificant responses. We then compared gene expression in the fetal lung, liver and hippocampus between oral Beta-P and the clinical treatment by RNA-sequencing. The transcriptomes were largely similar with small gene expression differences in the lung and liver, and no differences in the hippocampus between the groups. As proof of principle, ACS therapy can be effective using inexpensive and widely available oral drugs. Clinical dosing strategies must carefully consider the pharmacokinetics of oral Beta-P or Dex-P to minimize fetal exposure while achieving the desired treatment responses
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