6,672 research outputs found

    Production spectrum of high energy electrons from high energy cosmic ray collisions

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    Production spectrum of high energy electrons from high energy cosmic ray collision

    Delay in diabetic retinopathy screening increases the rate of detection of referable diabetic retinopathy

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    Aims - To assess whether there is a relationship between delay in retinopathy screening after diagnosis of Type 2 diabetes and level of retinopathy detected. Methods - Patients were referred from 88 primary care practices to an English National Health Service diabetic eye screening programme. Data for screened patients were extracted from the primary care databases using semi-automated data collection algorithms supplemented by validation processes. The programme uses two-field mydriatic digital photographs graded by a quality assured team. Results - Data were available for 8183 screened patients with diabetes newly diagnosed in 2005, 2006 or 2007. Only 163 with Type 1 diabetes were identified and were insufficient for analysis. Data were available for 8020 with newly diagnosed Type 2 diabetes. Of these, 3569 were screened within 6 months, 2361 between 6 and 11 months, 1058 between 12 and 17 months, 366 between 18 and 23 months, 428 between 24 and 35 months, and 238 at 3 years or more after diagnosis. There were 5416 (67.5%) graded with no retinopathy, 1629 (20.3%) with background retinopathy in one eye, 753 (9.4%) with background retinopathy in both eyes and 222 (2.8%) had referable diabetic retinopathy. There was a significant trend (P = 0.0004) relating time from diagnosis to screening detecting worsening retinopathy. Of those screened within 6 months of diagnosis, 2.3% had referable retinopathy and, 3 years or more after diagnosis, 4.2% had referable retinopathy. Conclusions - The rate of detection of referable diabetic retinopathy is elevated in those who were not screened promptly after diagnosis of Type 2 diabetes

    A DSMC investigation of gas flows in micro-channels with bends

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    Pressure-driven, implicit boundary conditions are implemented in an open source direct simulation Monte Carlo (DSMC) solver, and benchmarked against simple micro-channel flow cases found in the literature. DSMC simulations are then carried out of gas flows for varying degrees of rarefaction along micro-channels with both one and two ninety-degree bends. The results are compared to those from the equivalent straight micro-channel geometry. Away from the immediate bend regions, the pressure and Mach number profiles do not differ greatly from those in straight channels, indicating that there are no significant losses introduced when a bend is added to a micro-channel geometry. It is found that the inclusion of a bend in a micro-channel can increase the amount of mass that a channel can carry, and that adding a second bend produces a greater mass flux enhancement. This increase happens within a small range of Knudsen number (0.02 Knin 0.08). Velocity slip and shear stress profiles at the channel walls are presented for the Knudsen showing the largest mass flux enhancement

    Voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces

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    The behaviour of two biological macromolecules, bovine pancreatic insulin and hen-egg-whitelysozyme (HEWL), at aqueous-organogel interfaces confined within an array of solid-state membrane micropores was investigated via cyclic voltammetry (CV). The behaviour observed is discussed in terms of possible charge transferring species and mass transport in the interfacial reaction. Comparison of CV results for HEWL, insulin, and the well-characterised model ion tetraethylammonium cation (TEA+) revealed that the biomacromolecules undergo an interfacial reaction comprising biomacromolecular adsorption and facilitated transfer of electrolyte anions from the organic phase to a protein layer on the aqueous side of the interface, whereas TEA+ undergoes a simple ion transfer process. Evidence for biomacromolecular adsorption on the aqueous side of the micro-interfaces is provided by comparison of the CVs for TEA+ ion transfer in the presence and absence of the biomacromolecules. Similar experiments in the presence of the low generation polypropylenimine tetraamine dendrimer, (DAB-AM-4), a smaller synthetic molecule, revealed it to be non-adsorbing. The behaviour of biological macromolecules at miniaturised aqueous-organogel interfaces involves adsorption on the aqueous side of the interface and transfer of organic phase electrolyte anions across the interface to associate with the adsorbed biomacro molecule. The data presented support the previously suggested mechanism forbiomacromolecular voltammetry at liquid-liquid interfaces, involving adsorption and facilitated ion-transfer of organic electrolyte anions

    The performance of differential pulse stripping voltammetry at micro-liquid-liquid interface arrays

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    Microporous silicon membranes were recently introduced to create hexagonally-patterned arrays ofmicro-scale interfaces between two immiscible electrolyte solutions (lITIES). In this report we presenta simulation study of the application of differential pulse stripping voltammetry (DPSV) using theselITIES arrays for ion sensing. Simulations showed that the stripping current for ion detection wasenhanced by use of relatively deep pores (i.e. a low pore aspect ratio) and a viscous organic phase. These factors decrease the speed of escape of the pre-concentrated ion from the organic side of the ITIES. The stripping current initially increased steeply with pre-concentration time but eventually reached a plateau. Experiments performed using a lITIES array with micropores of radius 26 lm, depth of 100 lm and with a gelified organic phase demonstrated the saturation of the stripping peak with increasing pre-concentration time for the DPSV detection of tetraethylammonium ion. The reasons for the saturations are discussed in terms of diffusion coefficients and depth of the micropores

    Immorality and Irrationality

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    Does immorality necessarily involve irrationality? The question is often taken to be among the deepest in moral philosophy. But apparently deep questions sometimes admit of deflationary answers. In this case we can make way for a deflationary answer by appealing to dualism about rationality, according to which there are two fundamentally distinct notions of rationality: structural rationality and substantive rationality. I have defended dualism elsewhere. Here, I’ll argue that it allows us to embrace a sensible – I will not say boring – moderate view about the relationship between immorality and irrationality: roughly, that immorality involves substantive irrationality, but not structural irrationality. I defend this moderate view, and argue that many of the arguments for less moderate views turn either on missing the distinction between substantive and structural rationality, or on misconstruing it

    Rationality as the Rule of Reason

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    The demands of rationality are linked both to our subjective normative perspective (given that rationality is a person-level concept) and to objective reasons or favoring relations (given that rationality is non-contingently authoritative for us). In this paper, I propose a new way of reconciling the tension between these two aspects: roughly, what rationality requires of us is having the attitudes that correspond to our take on reasons in the light of our evidence, but only if it is competent. I show how this view can account for structural rationality on the assumption that intentions and beliefs as such involve competent perceptions of downstream reasons, and explore various implications of the account

    Discolored1 (DSC1) is an ADP-Ribosylation Factor-GTPase Activating Protein Required to Maintain Differentiation of Maize Kernel Structures

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    The embryo and endosperm are the products of double fertilization and comprise the clonally distinct products of angiosperm seed development. Recessive mutations in the maize gene discolored1 (dsc1) condition inviable seed that are defective in both embryo and endosperm development. Here, detailed phenotypic analyses illustrate that discolored mutant kernels are able to establish, but fail to maintain, differentiated embryo, and endosperm structures. Development of the discolored mutant embryo and endosperm is normal albeit delayed, prior to the abortion and subsequent degeneration of all differentiated kernel structures. Using a genomic fragment that was previously isolated by transposon tagging, the full length dsc1 transcript is identified and shown to encode an ADP-ribosylation factor-GTPase activating protein (ARF-GAP) that co-localizes with the trans-Golgi network/early endosomes and the plasma membrane during transient expression assays in N. benthamiana leaves. DSC1 function during endomembrane trafficking and the maintenance of maize kernel differentiation is discussed
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