Acousto-optic tunable filters (AOTFs) optimised for operation in the 2-4μm region

Acousto-Optic Tunable Filters (AOTFs) are electronically-controlled bandpass optical filters. They are often preferred in applications in spectroscopy where their agility and rapid random-access tuning can be deployed to advantage. When used for spectral imaging a large aperture (typically 10mm or more) is desired in order to permit sufficient optical throughput. However, in the mid IR the λ2 dependence on RF drive power combined with the large aperture can prove to be a hurdle, often making them impractical for many applications beyond about 2μm. We describe and compare a series of specialised free-space configurations of AOTF made from single crystal tellurium dioxide, that require relatively low RF drive power. We report on AOTFs specifically optimised for operation with a new generation of Supercontinuum source operating in the 2-4μm window and show how these may be used in a spectral imaging system. Finally, we describe an AOTF with an (acoustic) Fabry-Perot cavity operating at acoustic resonance rather than the conventional travelling-wave mode; the acoustic power requirement therefore being reduced. We present an analysis of the predicted performance. In addition, we address the practical issues in deploying such a scheme and outline the design of a prototype "resonant AOTF" operating in the 1-2μm region

Acousto-optic tunable filters for imaging applications in the 2-4~μm with low RF drive power

The λ2 dependence on acoustic field intensity (and hence RF drive power) can render large aperture acousto-optic tunable filters impractical for many applications beyond about 2 μm. One potential technique for reducing the RF drive-power requirement is to configure an acousto-optic tunable filter such that the interaction region is at acoustic resonance. We describe an acousto-optic tunable filter that operates at resonance and present an analysis of the predicted performance. In addition, we address the practical issues in deploying such a scheme. Finally, we present results of a prototype "resonant acousto-optic tunable filter" operating in the 1-2 μm region

Vascular risk factors and diabetic neuropathy

Background: Other than glycemic control, there are no treatments for diabetic neuropathy. Thus, identifying potentially modifiable risk factors for neuropathy is crucial. We studied risk factors for the development of distal symmetric neuropathy in 1172 patients with type 1 diabetes mellitus from 31 centers participating in the European Diabetes (EURODIAB) Prospective Complications Study. Methods: Neuropathy was assessed at baseline (1989 to 1991) and at follow-up (1997 to 1999), with a mean (±SD) follow-up of 7.3±0.6 years. A standardized protocol included clinical evaluation, quantitative sensory testing, and autonomic-function tests. Serum lipids and lipoproteins, glycosylated hemoglobin, and the urinary albumin excretion rate were measured in a central laboratory. Results: At follow-up, neuropathy had developed in 276 of 1172 patients without neuropathy at baseline (23.5 percent). The cumulative incidence of neuropathy was related to the glycosylated hemoglobin value and the duration of diabetes. After adjustment for these factors, we found that higher levels of total and low-density lipoprotein cholesterol and triglycerides, a higher body-mass index, higher von Willebrand factor levels and urinary albumin excretion rate, hypertension, and smoking were all significantly associated with the cumulative incidence of neuropathy. After adjustment for other risk factors and diabetic complications, we found that duration of diabetes, current glycosylated hemoglobin value, change in glycosylated hemoglobin value during the follow-up period, body-mass index, and smoking remained independently associated with the incidence of neuropathy. Cardiovascular disease at baseline was associated with double the risk of neuropathy, independent of cardiovascular risk factors. Conclusions: This prospective study indicates that, apart from glycemic control, the incidence of neuropathy is associated with potentially modifiable cardiovascular risk factors, including a raised triglyceride level, body-mass index, smoking, and hypertension

Vascular risk factors and diabetic neuropathy

Background: Other than glycemic control, there are no treatments for diabetic neuropathy. Thus, identifying potentially modifiable risk factors for neuropathy is crucial. We studied risk factors for the development of distal symmetric neuropathy in 1172 patients with type 1 diabetes mellitus from 31 centers participating in the European Diabetes (EURODIAB) Prospective Complications Study. Methods: Neuropathy was assessed at baseline (1989 to 1991) and at follow-up (1997 to 1999), with a mean (±SD) follow-up of 7.3±0.6 years. A standardized protocol included clinical evaluation, quantitative sensory testing, and autonomic-function tests. Serum lipids and lipoproteins, glycosylated hemoglobin, and the urinary albumin excretion rate were measured in a central laboratory. Results: At follow-up, neuropathy had developed in 276 of 1172 patients without neuropathy at baseline (23.5 percent). The cumulative incidence of neuropathy was related to the glycosylated hemoglobin value and the duration of diabetes. After adjustment for these factors, we found that higher levels of total and low-density lipoprotein cholesterol and triglycerides, a higher body-mass index, higher von Willebrand factor levels and urinary albumin excretion rate, hypertension, and smoking were all significantly associated with the cumulative incidence of neuropathy. After adjustment for other risk factors and diabetic complications, we found that duration of diabetes, current glycosylated hemoglobin value, change in glycosylated hemoglobin value during the follow-up period, body-mass index, and smoking remained independently associated with the incidence of neuropathy. Cardiovascular disease at baseline was associated with double the risk of neuropathy, independent of cardiovascular risk factors. Conclusions: This prospective study indicates that, apart from glycemic control, the incidence of neuropathy is associated with potentially modifiable cardiovascular risk factors, including a raised triglyceride level, body-mass index, smoking, and hypertension

Classifying seabed sediment type using simulated tidal-induced bed shear stress

An ability to estimate the large-scale spatial variability of seabed sediment type in the absence of extensive observational data is valuable for many applications. In some physical (e.g., morphodynamic) models, knowledge of seabed sediment type is important for inputting spatially-varying bed roughness, and in biological studies, an ability to estimate the distribution of seabed sediment benefits habitat mapping (e.g., scallop dredging). Although shelf sea sediment motion is complex, driven by a combination of tidal currents, waves, and wind-driven currents, in many tidally energetic seas, such as the Irish Sea, long-term seabed sediment transport is dominated by tidal currents. We compare observations of seabed sediment grain size from 242 Irish Sea seabed samples with simulated tidal-induced bed shear stress from a three-dimensional tidal model (ROMS) to quantitatively define the relationship between observed grain size and simulated bed shear stress. With focus on the median grain size of well-sorted seabed sediment samples, we present predictive maps of the distribution of seabed sediment classes in the Irish Sea, ranging from mud to gravel. When compared with the distribution of well-sorted sediment classifications (mud, sand and gravel) from the British Geological Survey digital seabed sediment map of Irish Sea sediments (DigSBS250), this �grain size tidal current proxy� (GSTCP) correctly estimates the observed seabed sediment classification in over 73% of the area

Targeting Neutrophilic Inflammation using Polymersome-Mediated Cellular Delivery

Neutrophils are key effector cells in inflammation and play an important role in neutralizing invading pathogens. During inflammation resolution, neutrophils undergo apoptosis before they are removed by macrophages, but if apoptosis is delayed, neutrophils can cause extensive tissue damage and chronic disease. Promotion of neutrophil apoptosis is a potential therapeutic approach for treating persistent inflammation, yet neutrophils have proven difficult cells to manipulate experimentally. In this study, we deliver therapeutic compounds to neutrophils using biocompatible, nanometer-sized synthetic vesicles, or polymersomes, which are internalized by binding to scavenger receptors and subsequently escape the early endosome through a pH-triggered disassembly mechanism. This allows polymersomes to deliver molecules into the cell cytosol of neutrophils without causing cellular activation. After optimizing polymersome size, we show that polymersomes can deliver the cyclin-dependent kinase inhibitor (R)-roscovitine into human neutrophils to promote apoptosis in vitro. Finally, using a transgenic zebrafish model, we show that encapsulated (R)-roscovitine can speed up inflammation resolution in vivo more efficiently than the free drug. These results show that polymersomes are effective intracellular carriers for drug delivery into neutrophils. This has important consequences for the study of neutrophil biology and the development of neutrophil-targeted therapeutics

Seasonal forecasting of groundwater levels in principal aquifers of the United Kingdom

To date, the majority of hydrological forecasting studies have focussed on using medium-range (3–15 days) weather forecasts to drive hydrological models and make predictions of future river flows. With recent developments in seasonal (1–3 months) weather forecast skill, such as those from the latest version of the UK Met Office global seasonal forecast system (GloSea5), there is now an opportunity to use similar methodologies to forecast groundwater levels in more slowly responding aquifers on seasonal timescales. This study uses seasonal rainfall forecasts and a lumped groundwater model to simulate groundwater levels at 21 locations in the United Kingdom up to three months into the future. The results indicate that the forecasts have skill; outperforming a persistence forecast and demonstrating reliability, resolution and discrimination. However, there is currently little to gain from using seasonal rainfall forecasts over using site climatology for this type of application. Furthermore, the forecasts are not able to capture extreme groundwater levels, primarily because of inadequacies in the driving rainfall forecasts. The findings also show that the origin of forecast skill, be it from the meteorological input, groundwater model or initial condition, is site specific and related to the groundwater response characteristics to rainfall and antecedent hydro-meteorological conditions

LINC00507 Is Specifically Expressed in the Primate Cortex and Has Age-Dependent Expression Patterns

Over the past decade, there has been an increase in the appreciation of the role of non-coding RNA in the development of organism phenotype. It is possible to divide the non-coding elements of the transcriptome into three categories: short non-coding RNAs, circular RNAs and long non-coding RNAs. Long non-coding RNAs are those transcripts that are greater than 200 nts in length and lack any significant open reading frames that produce proteins greater then 100 amino acids. Long intervening non-coding RNAs (lincRNAs) are a subclass of long non-coding RNAs. In contrast to protein coding RNAs, lincRNAs are expressed in a more tissue- and species-specific manner. In particular, many lincRNAs are only conserved amongst higher primates. This coupled with the propensity of many lincRNAs to be expressed in the brain, suggests that they are in fact one of the major drivers of organism complexity. We analysed 39 lincRNAs that are expressed in the frontal cortex and identified LINC00507 as being expressed in a cortex-specific manner in non-human primates and humans. The expression patterns of LINC00507 appear to be age-dependent, suggesting it may be involved in brain development of higher primates. Moreover, the analysis of LINC00507 potential to bind ribosomes revealed that this previously identified non-coding transcript may harbour a micropeptide

Proton-Induced Background Studies for a Satellite Gamma-Ray Experiment

This work was supported by the National Science Foundation Grant NSF PHY 78-22774 A02 & A03 and by Indiana Universit

Exact Results on e+ e- --> e+ e- + 2 Photons at SLC/LEP Energies

We use the spinor methods of the CALKUL collaboration, as realized by Xu, Zhang and Chang, to calculate the differential cross section for e+ e- --> e+ e- + 2 photons for c.m.s. energies in the SLC/LEP regime. An explicit complete formula for the respective cross section is obtained. The leading log approximation is used to check the formula. Applications of the formula to high precision luminosity calculations at SLC/LEP are discussed.Comment: 16 pages(LaTeX), UTHEP-92-0601 (contains corrected figures