123 research outputs found
Energetics of the Einstein-Rosen spacetime
A study covering some aspects of the Einstein--Rosen metric is presented. The
electric and magnetic parts of the Weyl tensor are calculated. It is shown that
there are no purely magnetic E--R spacetimes, and also that a purely electric
E--R spacetime is necessarily static. The geodesics equations are found and
circular ones are analyzed in detail. The super--Poynting and the
``Lagrangian'' Poynting vectors are calculated and their expressions are found
for two specific examples. It is shown that for a pulse--type solution, both
expressions describe an inward radially directed flow of energy, far behind the
wave front. The physical significance of such an effect is discussed.Comment: 19 pages Latex.References added and updated.To appear in
Int.J.Theor.Phy
Status of a Supersymmetric Flavour Violating Solution to the Solar Neutrino Puzzle with Three Generations
We present a general study of a three neutrino flavour transition model based
on the supersymmetric interactions which violate R-parity. These interactions
induce flavour violating scattering reactions between solar matter and
neutrinos. The model does not contain any vacuum mass or mixing angle for the
first generation neutrino. Instead, the effective mixing in the first
generation is induced via the new interactions. The model provides a natural
interpretation of the atmospheric neutrino anomaly, and is consistent with
reactor experiments. We determine all R-parity violating couplings which can
contribute to the effective neutrino oscillations, and summarize the present
laboratory bounds. Independent of the specific nature of the (supersymmetric)
flavour violating model, the experimental data on the solar neutrino rates and
the recoil electron energy spectrum are inconsistent with the theoretical
predictions. The confidence level of the -analysis ranges between and . The incompatibility, is due to the new SNO
results, and excludes the present model. We conclude that a non-vanishing
vacuum mixing angle for the first generation neutrino is necessary in our
model. We expect this also to apply to the solutions based on other flavour
violating interactions having constraints of the same order of magnitude.Comment: 17 pages, Latex fil
Energy and Flux Measurements of Ultra-High Energy Cosmic Rays Observed During the First ANITA Flight
The first flight of the Antarctic Impulsive Transient Antenna (ANITA)
experiment recorded 16 radio signals that were emitted by cosmic-ray induced
air showers. For 14 of these events, this radiation was reflected from the ice.
The dominant contribution to the radiation from the deflection of positrons and
electrons in the geomagnetic field, which is beamed in the direction of motion
of the air shower. This radiation is reflected from the ice and subsequently
detected by the ANITA experiment at a flight altitude of 36km. In this paper,
we estimate the energy of the 14 individual events and find that the mean
energy of the cosmic-ray sample is 2.9 EeV. By simulating the ANITA flight, we
calculate its exposure for ultra-high energy cosmic rays. We estimate for the
first time the cosmic-ray flux derived only from radio observations. In
addition, we find that the Monte Carlo simulation of the ANITA data set is in
agreement with the total number of observed events and with the properties of
those events.Comment: Added more explanation of the experimental setup and textual
improvement
Is symmetry identity?
Wigner found unreasonable the "effectiveness of mathematics in the natural
sciences". But if the mathematics we use to describe nature is simply a coded
expression of our experience then its effectiveness is quite reasonable. Its
effectiveness is built into its design. We consider group theory, the logic of
symmetry. We examine the premise that symmetry is identity; that group theory
encodes our experience of identification. To decide whether group theory
describes the world in such an elemental way we catalogue the detailed
correspondence between elements of the physical world and elements of the
formalism. Providing an unequivocal match between concept and mathematical
statement completes the case. It makes effectiveness appear reasonable. The
case that symmetry is identity is a strong one but it is not complete. The
further validation required suggests that unexpected entities might be
describable by the irreducible representations of group theory
The Pediatric Cell Atlas: defining the growth phase of human development at single-cell resolution
Single-cell gene expression analyses of mammalian tissues have uncovered profound stage-specific molecular regulatory phenomena that have changed the understanding of unique cell types and signaling pathways critical for lineage determination, morphogenesis, and growth. We discuss here the case for a Pediatric Cell Atlas as part of the Human Cell Atlas consortium to provide single-cell profiles and spatial characterization of gene expression across human tissues and organs. Such data will complement adult and developmentally focused HCA projects to provide a rich cytogenomic framework for understanding not only pediatric health and disease but also environmental and genetic impacts across the human lifespan
The Antarctic Impulsive Transient Antenna Ultra-high Energy Neutrino Detector Design, Performance, and Sensitivity for 2006-2007 Balloon Flight
We present a detailed report on the experimental details of the Antarctic
Impulsive Transient Antenna (ANITA) long duration balloon payload, including
the design philosophy and realization, physics simulations, performance of the
instrument during its first Antarctic flight completed in January of 2007, and
expectations for the limiting neutrino detection sensitivity. Neutrino physics
results will be reported separately.Comment: 50 pages, 49 figures, in preparation for PR
Age at symptom onset and death and disease duration in genetic frontotemporal dementia : an international retrospective cohort study
Background: Frontotemporal dementia is a heterogenous neurodegenerative disorder, with about a third of cases being genetic. Most of this genetic component is accounted for by mutations in GRN, MAPT, and C9orf72. In this study, we aimed to complement previous phenotypic studies by doing an international study of age at symptom onset, age at death, and disease duration in individuals with mutations in GRN, MAPT, and C9orf72. Methods: In this international, retrospective cohort study, we collected data on age at symptom onset, age at death, and disease duration for patients with pathogenic mutations in the GRN and MAPT genes and pathological expansions in the C9orf72 gene through the Frontotemporal Dementia Prevention Initiative and from published papers. We used mixed effects models to explore differences in age at onset, age at death, and disease duration between genetic groups and individual mutations. We also assessed correlations between the age at onset and at death of each individual and the age at onset and at death of their parents and the mean age at onset and at death of their family members. Lastly, we used mixed effects models to investigate the extent to which variability in age at onset and at death could be accounted for by family membership and the specific mutation carried. Findings: Data were available from 3403 individuals from 1492 families: 1433 with C9orf72 expansions (755 families), 1179 with GRN mutations (483 families, 130 different mutations), and 791 with MAPT mutations (254 families, 67 different mutations). Mean age at symptom onset and at death was 49\ub75 years (SD 10\ub70; onset) and 58\ub75 years (11\ub73; death) in the MAPT group, 58\ub72 years (9\ub78; onset) and 65\ub73 years (10\ub79; death) in the C9orf72 group, and 61\ub73 years (8\ub78; onset) and 68\ub78 years (9\ub77; death) in the GRN group. Mean disease duration was 6\ub74 years (SD 4\ub79) in the C9orf72 group, 7\ub71 years (3\ub79) in the GRN group, and 9\ub73 years (6\ub74) in the MAPT group. Individual age at onset and at death was significantly correlated with both parental age at onset and at death and with mean family age at onset and at death in all three groups, with a stronger correlation observed in the MAPT group (r=0\ub745 between individual and parental age at onset, r=0\ub763 between individual and mean family age at onset, r=0\ub758 between individual and parental age at death, and r=0\ub769 between individual and mean family age at death) than in either the C9orf72 group (r=0\ub732 individual and parental age at onset, r=0\ub736 individual and mean family age at onset, r=0\ub738 individual and parental age at death, and r=0\ub740 individual and mean family age at death) or the GRN group (r=0\ub722 individual and parental age at onset, r=0\ub718 individual and mean family age at onset, r=0\ub722 individual and parental age at death, and r=0\ub732 individual and mean family age at death). Modelling showed that the variability in age at onset and at death in the MAPT group was explained partly by the specific mutation (48%, 95% CI 35\u201362, for age at onset; 61%, 47\u201373, for age at death), and even more by family membership (66%, 56\u201375, for age at onset; 74%, 65\u201382, for age at death). In the GRN group, only 2% (0\u201310) of the variability of age at onset and 9% (3\u201321) of that of age of death was explained by the specific mutation, whereas 14% (9\u201322) of the variability of age at onset and 20% (12\u201330) of that of age at death was explained by family membership. In the C9orf72 group, family membership explained 17% (11\u201326) of the variability of age at onset and 19% (12\u201329) of that of age at death. Interpretation: Our study showed that age at symptom onset and at death of people with genetic frontotemporal dementia is influenced by genetic group and, particularly for MAPT mutations, by the specific mutation carried and by family membership. Although estimation of age at onset will be an important factor in future pre-symptomatic therapeutic trials for all three genetic groups, our study suggests that data from other members of the family will be particularly helpful only for individuals with MAPT mutations. Further work in identifying both genetic and environmental factors that modify phenotype in all groups will be important to improve such estimates. Funding: UK Medical Research Council, National Institute for Health Research, and Alzheimer's Society
Compensation dispersion between and within hierarchical levels
This paper studies the dispersion around the expected compensation of workers before and after controlling for hierarchical positions in cross-section data samples. From data for Spanish managers, we find that this dispersion decreases with education and work experience before entering the current job and increases with job tenure. This finding contrasts with previous research that finds a positive association between compensation dispersion and education and work experience. We explain the new finding through a model of learning that separates compensation dispersion between jobs and within jobs (hierarchical positions). The model takes advantage of the information revealed when workers are promoted to their current hierarchical positions and allows for more robust tests of learning theories
Long-Baseline Neutrino Facility (LBNF) and Deep Underground Neutrino Experiment (DUNE) Conceptual Design Report Volume 2: The Physics Program for DUNE at LBNF
The Physics Program for the Deep Underground Neutrino Experiment (DUNE) at the Fermilab Long-Baseline Neutrino Facility (LBNF) is described
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