23 research outputs found
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Properties of transition metal-doped zinc chalcogenide crystals for tunable IR laser radiation
The spectroscopic properties of Cr{sup 2+}, Co{sup 2+}, and Ni{sup 2+}-doped single crystals of ZnS, ZnSe, and ZnTe have been investigated to understand their potential application as mid-IR tunable solid-state laser media. The spectroscopy indicated divalent Cr was the most favorable candidate for efficient room temperature lasing, and accordingly, a laser-pumped laser demonstration of Cr:ZnS and Cr:ZnSe has been performed. The lasers` output were peaked at {approximately} 2.35 {mu}m and the highest measured slope efficiencies were {approximately} 20% in both cases
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Spectroscopy and decay kinetics of Pr{sup 3+}-doped chloride crystals for 1300-nm optical amplifiers
Several Pr{sup 3+}-doped chloride crystals have been tested spectroscopically for suitability as 1300-nm optical amplifiers operating on the {sup 1}G{sub 4} - {sup 3}H{sub 5} transition. {sup 1}G{sub 4} lifetimes are much longer than in fluoride hosts, ranging up to 1300 {mu}sec and suggesting a near-unity luminescence quantum yield. Emission spectra are typically broad (FWHM {approximately} 70 nm) and include the 1310-nm zero-dispersion wavelength of standard telecommunications fiber
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New infrared solid state laser materials for CALIOPE
Tunable infrared laser light may serve as a useful means by which to detect the presence of the targeted effluents. Since optical parametric oscillators (OPOs) have proven to be a versatile method of generating coherent light from the ultraviolet to the mid-infrared, this technology is a promising choice by which to service the CALIOPE applications. In addition, since some uncertainty remains regarding the precise wavelengths and molecules that will be targeted, the deployment of OPOs retains the greatest amount of wavelength flexibility. Another approach that the authors are considering is that of generating tunable infrared radiation directly with a diode-pumped solid state laser (DPSSL). One important advantage of a DPSSL is that it offers flexible pulse format modes that can be tailored to meet the needs of a particular application and target molecule. On the other hand, direct generation by a tunable DPSSL will generally be able to cover a more limited wavelength range than is possible with OPO technology. In support of the CALIOPE objectives the authors are exploring the potential for laser action among a class of materials comprised of transition metal-doped zinc chalcogenide crystals (i.e., ZnS, ZnSe and ZnTe). The Cr{sup 2+}, Co{sup 2+} and Ni{sup 2+} dopants were selected as the most favorable candidates, on the basis of their documented spectral properties in the scientific literature. Thus far, the authors have characterized the absorption and emission properties of these ions in the ZnS and ZnSe crystals. The absorption spectra are used to determine the preferred wavelength at which the crystal should be pumped, while the emission spectra reveal the extent of the tuning range potentially offered by the material. In addition, measurements of the emission lifetime as a function of temperature turn out to be quite useful, since this data is suggestive of the room temperature emission yield
Measurement of in Vivo Lumbar Intervertebral Disc Pressure during Spinal Manipulation: A Feasibility Study
Vietnam's socio-economic development : a social science review
The small-bodied hominin Homo jloresiensis was recently identified at Liang Bua, Flores, Indonesia. Some researchers have argued that H. jloresiensis represents pathological individuals from a behaviorally modern Homo sapiens population, arguing in part that the stone-tools found in association are too advanced to have been manufactured by a nonmodern hominin. Here we show that the Pleistocene stone-tools from Flores, including Liang Bua, are technologically and morphologically similar to the 1.2-1.9 Mya OldowaniDeveloped Oldowan tools from Olduvai Gorge in Africa. The Pleistocene lithic technology on Flores was therefore within the capabilities of small-brained, nonmodern hominins
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: A genome-wide association study.
Background: Loss-of-function mutations in GRN cause frontotemporal lobar degeneration (FTLD). Patients with GRN mutations present with a uniform subtype of TAR DNA-binding protein 43 (TDP-43) pathology at autopsy (FTLD-TDP type A); however, age at onset and clinical presentation are variable, even within families. We aimed to identify potential genetic modifiers of disease onset and disease risk in GRN mutation carriers. Methods: The study was done in three stages: a discovery stage, a replication stage, and a meta-analysis of the discovery and replication data. In the discovery stage, genome-wide logistic and linear regression analyses were done to test the association of genetic variants with disease risk (case or control status) and age at onset in patients with a GRN mutation and controls free of neurodegenerative disorders. Suggestive loci (p<1 × 10−5) were genotyped in a replication cohort of patients and controls, followed by a meta-analysis. The effect of genome-wide significant variants at the GFRA2 locus on expression of GFRA2 was assessed using mRNA expression studies in cerebellar tissue samples from the Mayo Clinic brain bank. The effect of the GFRA2 locus on progranulin concentrations was studied using previously generated ELISA-based expression data. Co-immunoprecipitation experiments in HEK293T cells were done to test for a direct interaction between GFRA2 and progranulin. Findings: Individuals were enrolled in the current study between Sept 16, 2014, and Oct 5, 2017. After quality control measures, statistical analyses in the discovery stage included 382 unrelated symptomatic GRN mutation carriers and 1146 controls free of neurodegenerative disorders collected from 34 research centres located in the USA, Canada, Australia, and Europe. In the replication stage, 210 patients (67 symptomatic GRN mutation carriers and 143 patients with FTLD without GRN mutations pathologically confirmed as FTLD-TDP type A) and 1798 controls free of neurodegenerative diseases were recruited from 26 sites, 20 of which overlapped with the discovery stage. No genome-wide significant association with age at onset was identified in the discovery or replication stages, or in the meta-analysis. However, in the case-control analysis, we replicated the previously reported TMEM106B association (rs1990622 meta-analysis odds ratio [OR] 0·54, 95% CI 0·46–0·63; p=3·54 × 10−16), and identified a novel genome-wide significant locus at GFRA2 on chromosome 8p21.3 associated with disease risk (rs36196656 meta-analysis OR 1·49, 95% CI 1·30–1·71; p=1·58 × 10−8). Expression analyses showed that the risk-associated allele at rs36196656 decreased GFRA2 mRNA concentrations in cerebellar tissue (p=0·04). No effect of rs36196656 on plasma and CSF progranulin concentrations was detected by ELISA; however, co-immunoprecipitation experiments in HEK293T cells did suggest a direct binding of progranulin and GFRA2. Interpretation: TMEM106B-related and GFRA2-related pathways might be future targets for treatments for FTLD, but the biological interaction between progranulin and these potential disease modifiers requires further study. TMEM106B and GFRA2 might also provide opportunities to select and stratify patients for future clinical trials and, when more is known about their potential effects, to inform genetic counselling, especially for asymptomatic individuals. Funding: National Institute on Aging, National Institute of Neurological Disorders and Stroke, Canadian Institutes of Health Research, Italian Ministry of Health, UK National Institute for Health Research, National Health and Medical Research Council of Australia, and the French National Research Agency