382 research outputs found
Nodal superconducting gap structure in the quasi-one-dimensional CsCrAs investigated using SR measurements
The superconducting ground state of the newly discovered superconductor
CsCrAs with a quasi-one-dimensional crystal structure ( 2.1(1) K) has been investigated using magnetization and muon-spin
relaxation or rotation (SR), both zero-field (ZF) and transverse-field
(TF), measurements. Our ZF SR measurements reveal the presence of spin
fluctuations below 4 K and the ZF relaxation rate () shows enhancement
below 2.1 K, which might indicate that the superconducting
state is unconventional. This observation suggests that the electrons are
paired via unconventional channels such as spin fluctuations, as proposed on
the basis of theoretical models. Our analysis of the TF SR results shows
that the temperature dependence of the superfluid density is fitted better with
a nodal gap structure than an isotropic s-wave model for the superconducting
gap. The observation of a nodal gap in CsCrAs is consistent with
that observed in the isostructural KCrAs compound through TF
SR measurements. Furthermore, from our TF SR study we have estimated
the magnetic penetration depth = 954 nm,
superconducting carrier density m, and
carrier's effective-mass enhancement = 1.61m.Comment: 7 pages, 4 figures. arXiv admin note: substantial text overlap with
arXiv:1505.0574
Track Reconstruction and Performance of DRIFT Directional Dark Matter Detectors using Alpha Particles
First results are presented from an analysis of data from the DRIFT-IIa and
DRIFT-IIb directional dark matter detectors at Boulby Mine in which alpha
particle tracks were reconstructed and used to characterise detector
performance--an important step towards optimising directional technology. The
drift velocity in DRIFT-IIa was [59.3 +/- 0.2 (stat) +/- 7.5 (sys)] m/s based
on an analysis of naturally-occurring alpha-emitting background. The drift
velocity in DRIFT-IIb was [57 +/- 1 (stat) +/- 3 (sys)] m/s determined by the
analysis of alpha particle tracks from a Po-210 source. 3D range reconstruction
and energy spectra were used to identify alpha particles from the decay of
Rn-222, Po-218, Rn-220 and Po-216. This study found that (22 +/- 2)% of Po-218
progeny (from Rn-222 decay) are produced with no net charge in 40 Torr CS2. For
Po-216 progeny (from Rn-220 decay) the uncharged fraction is (100 +0 -35)%.Comment: 27 pages, 12 figures, 5 tables. Submitted to Nuclear Instruments and
Methods in Physics Research, Section A. Subj-class: Instrumentation and
Detector
Dementia diagnostic criteria in Down syndrome
Objective: Dementia is a common clinical presentation among older adults with Down syndrome. The presentation of dementia in Down syndrome differs compared with typical Alzheimer's disease. The performance of manualised dementia criteria in the International Classification of Diseases (ICD)-10 and Diagnostic and Statistical Manual of Mental Disorders-IV-Text Revision (DSM-IV-TR) is uncertain in this population.We aimed to determine the concurrent validity and reliability of clinicians' diagnoses of dementia against ICD-10 and DSM-IV-TR diagnoses. Validity of clinical diagnoses were also explored by establishing the stability of diagnoses over time. / Methods: We used clinical data from memory assessments of 85 people with Down syndrome, of whom 64 (75.3%) had a diagnosis of dementia. The cases of dementia were presented to expert raters who rated the case as dementia or no dementia using ICD-10 and DSM-IV-TR criteria and their own clinical judgement. / Results: We found that clinician's judgement corresponded best with clinically diagnosed cases of dementia, identifying 84.4% cases of clinically diagnosed dementia at the time of diagnosis. ICD-10 criteria identified 70.3% cases, and DSM-IV-TR criteria identified 56.3% cases at the time of clinically diagnosed dementia. Over time, the proportion of cases meeting ICD-10 or DSM-IV-TR diagnoses increased, suggesting that experienced clinicians used their clinical knowledge of dementia presentation in Down syndrome to diagnose the disorder at an earlier stage than would have been possible had they relied on the classic description contained in the diagnostic systems. / Conclusions: Clinical diagnosis of dementia in Down syndrome is valid and reliable and can be used as the standard against which new criteria such as the DSM-5 are measured
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