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1.
Phys Rev Lett ; 131(22): 221801, 2023 Dec 01.
Article in English | MEDLINE | ID: mdl-38101357

ABSTRACT

Using an 185-kg NaI[Tl] array, COHERENT has measured the inclusive electron-neutrino charged-current cross section on ^{127}I with pion decay-at-rest neutrinos produced by the Spallation Neutron Source at Oak Ridge National Laboratory. Iodine is one the heaviest targets for which low-energy (≤50 MeV) inelastic neutrino-nucleus processes have been measured, and this is the first measurement of its inclusive cross section. After a five-year detector exposure, COHERENT reports a flux-averaged cross section for electron neutrinos of 9.2_{-1.8}^{+2.1}×10^{-40} cm^{2}. This corresponds to a value that is ∼41% lower than predicted using the MARLEY event generator with a measured Gamow-Teller strength distribution. In addition, the observed visible spectrum from charged-current scattering on ^{127}I has been measured between 10 and 55 MeV, and the exclusive zero-neutron and one-or-more-neutron emission cross sections are measured to be 5.2_{-3.1}^{+3.4}×10^{-40} and 2.2_{-0.5}^{+0.4}×10^{-40} cm^{2}, respectively.

2.
Phys Rev Lett ; 130(5): 051803, 2023 Feb 03.
Article in English | MEDLINE | ID: mdl-36800477

ABSTRACT

The COHERENT Collaboration searched for scalar dark matter particles produced at the Spallation Neutron Source with masses between 1 and 220 MeV/c^{2} using a CsI[Na] scintillation detector sensitive to nuclear recoils above 9 keV_{nr}. No evidence for dark matter is found and we thus place limits on allowed parameter space. With this low-threshold detector, we are sensitive to coherent elastic scattering between dark matter and nuclei. The cross section for this process is orders of magnitude higher than for other processes historically used for accelerator-based direct-detection searches so that our small, 14.6 kg detector significantly improves on past constraints. At peak sensitivity, we reject the flux consistent with the cosmologically observed dark-matter concentration for all coupling constants α_{D}<0.64, assuming a scalar dark-matter particle. We also calculate the sensitivity of future COHERENT detectors to dark-matter signals which will ambitiously test multiple dark-matter spin scenarios.

3.
Phys Rev Lett ; 129(8): 081801, 2022 Aug 19.
Article in English | MEDLINE | ID: mdl-36053683

ABSTRACT

We measured the cross section of coherent elastic neutrino-nucleus scattering (CEvNS) using a CsI[Na] scintillating crystal in a high flux of neutrinos produced at the Spallation Neutron Source at Oak Ridge National Laboratory. New data collected before detector decommissioning have more than doubled the dataset since the first observation of CEvNS, achieved with this detector. Systematic uncertainties have also been reduced with an updated quenching model, allowing for improved precision. With these analysis improvements, the COHERENT Collaboration determined the cross section to be (165_{-25}^{+30})×10^{-40} cm^{2}, consistent with the standard model, giving the most precise measurement of CEvNS yet. The timing structure of the neutrino beam has been exploited to compare the CEvNS cross section from scattering of different neutrino flavors. This result places leading constraints on neutrino nonstandard interactions while testing lepton flavor universality and measures the weak mixing angle as sin^{2}θ_{W}=0.220_{-0.026}^{+0.028} at Q^{2}≈(50 MeV)^{2}.

4.
Phys Rev Lett ; 125(13): 131803, 2020 Sep 25.
Article in English | MEDLINE | ID: mdl-33034491

ABSTRACT

We report the first precision measurement of the parity-violating asymmetry in the direction of proton momentum with respect to the neutron spin, in the reaction ^{3}He(n,p)^{3}H, using the capture of polarized cold neutrons in an unpolarized active ^{3}He target. The asymmetry is a result of the weak interaction between nucleons, which remains one of the least well-understood aspects of electroweak theory. The measurement provides an important benchmark for modern effective field theory and potential model calculations. Measurements like this are necessary to determine the spin-isospin structure of the hadronic weak interaction. Our asymmetry result is A_{PV}=[1.55±0.97(stat)±0.24(sys)]×10^{-8}, which has the smallest uncertainty of any hadronic parity-violating asymmetry measurement so far.

5.
Eur J Neurol ; 25(5): 790-794, 2018 05.
Article in English | MEDLINE | ID: mdl-29437287

ABSTRACT

BACKGROUND AND PURPOSE: The aim was to determine the genetic background of unknown muscular dystrophy in five French families. METHODS: Twelve patients with limb girdle muscular dystrophy or distal myopathy were clinically evaluated. Gene mutations were identified using targeted exon sequencing and mutated DNAJB6 was tested in vitro. RESULTS: Five patients presented with distal lower limb weakness whilst others had proximal presentation with a variable rate of progression starting at the mean age of 38.5 years. Two novel mutations (c.284A>T, p.Asn95Ile, two families; and c.293_295delATG, p.Asp98del, one family) as well as the previously reported c.279C>G (p.Phe93Leu, two families) mutation in DNAJB6 were identified. All showed a reduced capacity to prevent protein aggregation. CONCLUSIONS: The mutational and phenotypical spectrum of DNAJB6-caused muscle disease is larger than previously reported, including also dysphagia. The originally reported c.279C>G (p.Phe93Leu) mutation is now identified in four different populations and appears to be a mutational hotspot. Our report confirms that some DNAJB6 mutations cause distal-onset myopathy and hence DNAJB6 defects should be considered broadly in dominant muscular dystrophy families.


Subject(s)
Distal Myopathies/genetics , HSP40 Heat-Shock Proteins/genetics , Molecular Chaperones/genetics , Muscular Dystrophies, Limb-Girdle/genetics , Mutation , Nerve Tissue Proteins/genetics , Adult , Aged , Aged, 80 and over , Disease Progression , Female , France , Humans , Male , Middle Aged , Muscle Weakness/genetics , Pedigree , Phenotype
6.
Neuropathol Appl Neurobiol ; 44(5): 441-448, 2018 08.
Article in English | MEDLINE | ID: mdl-28489263

ABSTRACT

AIMS: Previously, detection of ANO5 protein has been complicated by unspecific antibodies, most of which have not identified the correct protein. The aims of the study were to specify ANO5 protein expression in human skeletal muscle, and to investigate if the ANO5 protein levels are affected by different ANO5 mutations in anoctaminopathy patients. METHODS: Four different antibodies were tested for ANO5 specificity. A sample preparation method compatible with membrane proteins, combined with tissue fractionation was used to determine ANO5 expression in cell cultures expressing ANO5, in normal muscles and eight patient biopsies with six different ANO5 mutations in homozygous or compound heterozygous states, and in other dystrophies. RESULTS: Only one specific monoclonal N-terminal ANO5 antibody was efficient in detecting the protein, showing that ANO5 is expressed as a single 107 kD polypeptide in human skeletal muscle. The truncating mutations c.191dupA and c.1261C>T were found to abolish ANO5 expression, whereas the studied point mutations had variable effects; however, all the ANO5 mutations resulted in clearly reduced ANO5 expression in the patient muscle membrane fraction. Attempts to detect ANO5 using immunohistochemistry were not yet successful. CONCLUSIONS: The data presented here indicate that the ANO5 protein expression is decreased in ANO5-mutated muscular dystrophy and that most of the non-truncating pathogenic ANO5 mutations likely destabilize the protein and cause its degradation. The method described here allows direct analysis of human ANO5 protein, which can be used in diagnostics, for evaluating the pathogenicity of the potentially harmful ANO5 variants of uncertain significance.


Subject(s)
Anoctamins/analysis , Anoctamins/genetics , Anoctamins/metabolism , Muscular Dystrophies, Limb-Girdle/diagnosis , Muscular Dystrophies, Limb-Girdle/genetics , Antibodies, Monoclonal , Antibody Specificity , Blotting, Western/methods , Female , Humans , Male , Mutation
7.
Phys Rev Lett ; 121(24): 242002, 2018 Dec 14.
Article in English | MEDLINE | ID: mdl-30608729

ABSTRACT

We report the first observation of the parity-violating gamma-ray asymmetry A_{γ}^{np} in neutron-proton capture using polarized cold neutrons incident on a liquid parahydrogen target at the Spallation Neutron Source at Oak Ridge National Laboratory. A_{γ}^{np} isolates the ΔI=1, ^{3}S_{1}→^{3}P_{1} component of the weak nucleon-nucleon interaction, which is dominated by pion exchange and can be directly related to a single coupling constant in either the DDH meson exchange model or pionless effective field theory. We measured A_{γ}^{np}=[-3.0±1.4(stat)±0.2(syst)]×10^{-8}, which implies a DDH weak πNN coupling of h_{π}^{1}=[2.6±1.2(stat)±0.2(syst)]×10^{-7} and a pionless EFT constant of C^{^{3}S_{1}→^{3}P_{1}}/C_{0}=[-7.4±3.5(stat)±0.5(syst)]×10^{-11} MeV^{-1}. We describe the experiment, data analysis, systematic uncertainties, and implications of the result.

8.
Neurology ; 78(12): 897-903, 2012 Mar 20.
Article in English | MEDLINE | ID: mdl-22402862

ABSTRACT

OBJECTIVE: Description of 8 new ANO5 mutations and significant expansion of the clinical phenotype spectrum associated with previously known and unknown mutations to improve diagnostic accuracy. METHODS: DNA samples of 101 patients in 95 kindreds at our quaternary referral center in Finland, who had undetermined limb-girdle muscular dystrophy (LGMD), calf distal myopathy, or creatine kinase (CK) elevations of more than 2,000 IU/L, were selected for ANO5 genetic evaluation, and the clinical findings of patients with mutations were retrospectively analyzed. RESULTS: A total of 25 patients with muscular dystrophy caused by 11 different recessive mutations in the ANO5 gene were identified. The vast majority of mutations, 8 of 11, proved to be previously unknown new mutations. The most frequent mutation, c.2272C>T (p.R758C), was present in 20 patients. The phenotypes associated with this and the common European mutation, c.191dupA, varied from nearly asymptomatic high hyperCKemia to severe LGMD with consistently milder phenotypes in female patients. CONCLUSIONS: Mutations in ANO5 are a frequent cause of undetermined muscular dystrophy, with both distal and proximal presentation. Other types include high hyperCKemia, myalgia, or calf hypertrophy over decades without significant weakness, especially in female patients. Mutations are distributed all over the gene, indicating that muscular dystrophy caused by ANO5 can be expected to occur in all populations.


Subject(s)
Chloride Channels/genetics , Muscular Dystrophies, Limb-Girdle/genetics , Muscular Dystrophies, Limb-Girdle/pathology , Mutation/physiology , Adult , Age of Onset , Aged , Anoctamins , Blotting, Western , Cohort Studies , Creatine Kinase/blood , DNA/genetics , Female , Finland , Genes, Recessive , Genetic Testing , Genetic Variation , Genotype , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Muscle Weakness/etiology , Muscle, Skeletal/pathology , Muscular Dystrophies, Limb-Girdle/diagnosis , Phenotype , Reproducibility of Results
10.
Neurology ; 77(4): 334-40, 2011 Jul 26.
Article in English | MEDLINE | ID: mdl-21715705

ABSTRACT

OBJECTIVE: Characterization of a new type of late-onset autosomal dominant lower motor neuron disease. METHODS: Patients from 2 families underwent detailed neurologic, electrophysiologic, muscle biopsy, and laboratory investigations. MRI of lower limbs was performed in selected patients. DNA samples from leukocytes were used for molecular genetic linkage studies. RESULTS: First symptoms were muscle cramps and fasciculations after age 25-30, followed by a slowly progressive proximal and distal weakness without overt atrophy during the first decades of symptoms. Nerve conduction velocities were within normal range and EMG showed widespread neurogenic alterations. Muscle biopsy revealed characteristic neurogenic findings: fiber type grouping and group atrophy. MRI showed diffuse fatty-degenerative changes, marked in medial gastrocnemius. CONCLUSION: Exactly the same clinical phenotype has not previously been described, and linkage studies showed exclusion of known chromosomal loci for hereditary motor neuropathies, suggesting the disease we report may represent a new disorder.


Subject(s)
Chromosome Disorders/epidemiology , Chromosome Disorders/genetics , Motor Neuron Disease/epidemiology , Motor Neuron Disease/genetics , Adult , Age of Onset , Chromosome Disorders/complications , Chromosome Disorders/diagnosis , Chromosome Disorders/pathology , Chromosome Disorders/physiopathology , Electromyography , Female , Genetic Linkage , Humans , Male , Middle Aged , Motor Neuron Disease/complications , Motor Neuron Disease/diagnosis , Motor Neuron Disease/pathology , Motor Neuron Disease/physiopathology , Muscle, Skeletal/pathology , Muscular Atrophy/complications , Neural Conduction/physiology , Pedigree , Phenotype
11.
Phys Rev Lett ; 101(8): 083002, 2008 Aug 22.
Article in English | MEDLINE | ID: mdl-18764610

ABSTRACT

We have observed depolarization effects when high intensity cold neutron beams are incident on alkali-metal spin-exchange-polarized 3He cells used as neutron spin filters. This was first observed as a reduction of the maximum attainable 3He polarization and was attributed to a decrease of alkali-metal polarization, which led us to directly measure alkali-metal polarization and spin relaxation over a range of neutron fluxes at Los Alamos Neutron Science Center and Institute Laue-Langevin. The data reveal a new alkali-metal spin-relaxation mechanism that approximately scales as sqrt[phi_{n}], where phi_{n} is the neutron capture-flux density incident on the cell. This is consistent with an effect proportional to the concentration of electron-ion pairs but is much larger than expected from earlier work.

12.
J Res Natl Inst Stand Technol ; 110(3): 195-203, 2005.
Article in English | MEDLINE | ID: mdl-27308121

ABSTRACT

The NPDGamma experiment will measure the parity-violating directional gamma ray asymmetry A γ in the reaction [Formula: see text]. Ultimately, this will constitute the first measurement in the neutron-proton system that is sensitive enough to challenge modern theories of nuclear parity violation, providing a theoretically clean determination of the weak pion-nucleon coupling. A new beam-line at the Los Alamos Neutron Science Center (LANSCE) delivers pulsed cold neutrons to the apparatus, where they are polarized by transmission through a large volume polarized (3)He spin filter and captured in a liquid para-hydrogen target. The 2.2 MeV gamma rays from the capture reaction are detected in an array of CsI(Tl) scintillators read out by vacuum photodiodes operated in current mode. We will complete commissioning of the apparatus and carry out a first measurement at LANSCE in 2004-05, which would provide a statistics-limited result for A γ accurate to a standard uncertainty of ±5 × 10(-8) level or better, improving on existing measurements in the neutron-proton system by a factor of 4. Plans to move the experiment to a reactor facility, where the greater flux would enable us to make a measurement with a standard uncertainty of ±1 × 10(-8), are actively being pursued for the longer term.

13.
J Res Natl Inst Stand Technol ; 110(3): 215-9, 2005.
Article in English | MEDLINE | ID: mdl-27308124

ABSTRACT

The NPDGamma γ-ray detector has been built to measure, with high accuracy, the size of the small parity-violating asymmetry in the angular distribution of gamma rays from the capture of polarized cold neutrons by protons. The high cold neutron flux at the Los Alamos Neutron Scattering Center (LANSCE) spallation neutron source and control of systematic errors require the use of current mode detection with vacuum photodiodes and low-noise solid-state preamplifiers. We show that the detector array operates at counting statistics and that the asymmetries due to B4C and (27)Al are zero to with- in 2 × 10(-6) and 7 × 10(-7), respectively. Boron and aluminum are used throughout the experiment. The results presented here are preliminary.

14.
J Res Natl Inst Stand Technol ; 110(3): 145-8, 2005.
Article in English | MEDLINE | ID: mdl-27308111

ABSTRACT

The NPDGamma collaboration has completed the construction of a pulsed cold neutron beam line on flight path12 at the Los Alamos Neutron Science Center (LANSCE). We describe the new beam line and characteristics of the beam. We report results of the moderator brightness and the guide performance measurements. FP12 has the highest pulsed cold neutron intensity for nuclear physics in the world.

15.
J Res Natl Inst Stand Technol ; 110(3): 309-13, 2005.
Article in English | MEDLINE | ID: mdl-27308142

ABSTRACT

The abBA collaboration is developing a new type of field-expansion spectrometer for a measurement of the three correlation coefficients a, A, and B and the shape parameter b. The measurement of A and B requires precision neutron polarimetry. We will polarize a pulsed cold neutron beam from the SNS using a (3)He neutron spin filter. The well-known polarizing cross section for n-(3)He has a 1/v dependence, where v is the neutron velocity, which is used to determine the absolute beam polarization through a time-of-flight (TOF) measurement. We show that by measuring the TOF dependence of A and B, the coefficients and the neutron polarization can be determined with a small loss of the statistical precision and with negligible systematic error. We conclude that it is possible to determine the neutron polarization averaged over a long run in the neutron beta decay experiment with a statistical error less than 10(-4). We discuss various sources of systematic uncertainty in the measurement of A and B and conclude that the fractional systematic errors are less than 2 × 10(-4).

16.
J Res Natl Inst Stand Technol ; 110(4): 361-6, 2005.
Article in English | MEDLINE | ID: mdl-27308151

ABSTRACT

We present a conceptual design for an experiment to measure the neutron lifetime (~886 s) with an accuracy of 10(-4). The lifetime will be measured by observing the decay rate of a sample of ultracold neutrons (UCN) confined in vacuum in a magnetic trap. The UCN collaboration at Los Alamos National Laboratory has developed a prototype UCN source that is expected to produce a bottled UCN density of more than 100/cm(3) [1]. The availability of such an intense source makes it possible to approach the measurement of the neutron lifetime in a new way. We argue below that it is possible to measure the neutron lifetime to 10(-4) in a vacuum magnetic trap. The measurement involves no new technology beyond the expected UCN density. If even higher densities are available, the experiment can be made better and/or less expensive. We present the design and methodology for the measurement. The slow loss of neutrons that have stable orbits, but are not energetically trapped would produce a systematic uncertainty in the measurement. We discuss a new approach, chaotic cleaning, to the elimination of quasi-neutrons from the trap by breaking the rotational symmetry of the quadrupole trap. The neutron orbits take on a chaotic character and mode mixing causes the neutrons on the quasi-bound orbits to leave the trap.

17.
J Res Natl Inst Stand Technol ; 110(4): 389-93, 2005.
Article in English | MEDLINE | ID: mdl-27308155

ABSTRACT

We are developing an experiment to measure the correlations a, A, and B, and the Fierz interference term b in neutron decay, with a precision of approximately 10(-4). The experiment uses an electromagnetic spectrometer in combination with two large-area segmented silicon detectors to detect the proton and electron from the decay in coincidence, with 4π acceptance for both particles. For the neutron-polarization-dependent observables A and B, precision neutron polarimetry is achieved through the combination of a pulsed neutron beam, under construction at the SNS, and a polarized (3)He neutron polarizer. Measuring a and A in the same apparatus provides a redundant determination of λ = gA/gV . Uncertainty in λ dominates the uncertainty of CKM unitarity tests.

18.
J Res Natl Inst Stand Technol ; 110(4): 427-9, 2005.
Article in English | MEDLINE | ID: mdl-27308162

ABSTRACT

We have developed a new type of field-expansion spectrometer to measure the neutron beta decay correlations (a, b, B, and A). A precision measurement of these correlations places stringent requirements on charged particle detectors. The design employs large area segmented silicon detectors to detect both protons and electrons in coincidence. Other requirements include good energy resolution (< 5 keV), a thin dead layer to allow observation of 30-keV protons, fast timing resolution (~1 ns) to reconstruct electron-backscattering events, and nearly unity efficiency. We report results of testing commercially available surface-barrier silicon detectors for energy resolution and timing performance, and measurement of the dead-layer thickness of ion-implanted silicon detectors with a 3.2 MeV alpha source.

19.
Phys Rev Lett ; 93(10): 105302, 2004 Sep 03.
Article in English | MEDLINE | ID: mdl-15447413

ABSTRACT

We describe a neutron radiography technique that can be used to map the distribution of 3He impurities in liquid 4He, providing direct and quantitative access to underlying transport processes. Images reflecting finite normal- and superfluid-component 4He velocity fields are presented.

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