109 research outputs found

    Luminous Intensity for Traffic Signals: A Scientific Basis for Performance Specifications

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    Humnan factors experiments on visual responses to simulated traffic signals using incandescent lamps and light-emitting diodes are described

    Massive sulphide deposits of the Central Jebilet Massif, Morocco

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    The Central Jebilet massif, in the Marrakech region of Morocco, comprises a block of Carboniferous sedimentary rocks that were extensively deformed and metamorphosed during the Variscan orogeny. This block, and its extension to the south of Marrakech (the Guemassa massif), are characterised by bimodal intrusive magmatism and abundant massive sulphide deposits that represent a major Cu-Pb-Zn resource. Mining is currently taking place at the Draa Sfar and Hajjar mines. Previously worked deposits at Kettara, Roc Blanc and Koudiat Aicha are not currently being exploited, but have extensive reserves remaining, and prospects such as Laachach and Ben Slimane are being explored

    Release of dissolved organic carbon from seagrass wrack and its implications for trophic connectivity

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    ABSTRACT: The export of old leaves and stems (wrack) from seagrass meadows provides a mechanism for trophic connectivity among coastal ecosystems. As little of this wrack is consumed by mesograzers, leached dissolved organic carbon (DOC) may determine the importance of wrack as a trophic subsidy. However, few studies have examined the effect of seagrass type or age on the release of DOC or its bioavailability. We examined the amount and composition of DOC released from different wrack: Posidonia sinuosa, Amphibolis antarctica and the alga Laurencia sp. We then examined the effect of age on DOC leaching from P. sinuosa wrack. The bioavailability of the DOC was also assessed using a bacterial bioassay. The rate of DOC leaching from P. sinuosa leaves decreased exponentially with time. According to that exponential model, ~50% of the total DOC release occurred in the first 14 d and it would require a further 2.94 yr to release the same amount again. Fresh algae Laurencia sp. leached the greatest amount of DOC in the first 16 h (6.7 g kg-1 fresh weight (FW) wrack), followed by fresh P. sinuosa leaves (1.7 g kg-1 FW), A. antarctica leaves (1.1 g kg-1) and stems (0.6 g kg-1), 4 wk old P. sinuosa (67 g kg-1) and fine detritus (74 g kg-1). In all cases, the composition of the DOC was similar and dominated by the hydrophilic component (in P. sinuosa, predominantly sugars and amino acids). Leachates from all fresh wrack supported bacterial growth over 24 h. Leachate from older wrack either failed to support bacterial growth or only supported it for a limited time. Given the exponential decay in DOC release rate, the interacting timescales of transport and leaching will affect the value of wrack as a vector for trophic subsidies

    Auto-validation of fluorescent primer extension genotyping assay using signal clustering and neural networks

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    BACKGROUND: SNP genotyping typically incorporates a review step to ensure that the genotype calls for a particular SNP are correct. For high-throughput genotyping, such as that provided by the GenomeLab SNPstream(® )instrument from Beckman Coulter, Inc., the manual review used for low-volume genotyping becomes a major bottleneck. The work reported here describes the application of a neural network to automate the review of results. RESULTS: We describe an approach to reviewing the quality of primer extension 2-color fluorescent reactions by clustering optical signals obtained from multiple samples and a single reaction set-up. The method evaluates the quality of the signal clusters from the genotyping results. We developed 64 scores to measure the geometry and position of the signal clusters. The expected signal distribution was represented by a distribution of a 64-component parametric vector obtained by training the two-layer neural network onto a set of 10,968 manually reviewed 2D plots containing the signal clusters. CONCLUSION: The neural network approach described in this paper may be used with results from the GenomeLab SNPstream instrument for high-throughput SNP genotyping. The overall correlation with manual revision was 0.844. The approach can be applied to a quality review of results from other high-throughput fluorescent-based biochemical assays in a high-throughput mode

    The Association of Coloproctology of Great Britain and Ireland consensus guidelines in emergency colorectal surgery

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    ACKNOWLEDGEMENTS Review and editing: S.R. Brown, Professor of Surgery, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK. Email [email protected]. Patient summary: R.G. Arnott, Retired Professor, Patient Liaison Group, Association of Coloproctology of Great Britain and Ireland, Royal College of Surgeons of England, London, UK. Email [email protected]. Delphi review: C.P. Macklin. BMedSci BM BS FRCS DM, Consultant Colorectal Surgeon, Mid Yorkshire Hospitals, UK. Email [email protected] reviewedPublisher PD

    CAG expansion affects the expression of mutant huntingtin in the Huntington's disease brain

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    AbstractA trinucleotide repeat (CAG) expansion in the huntingtin gene causes Huntington's disease (HD). In brain tissue from HD heterozygotes with adult onset and more clinically severe juvenile onset, where the largest expansions occur, a mutant protein of equivalent intensity to wild-type huntingtin was detected in cortical synaptosomes, indicating that a mutant species is synthesized and transported with the normal protein to nerve endings. The increased size of mutant huntingtin relative to the wild type was highly correlated with CAG repeat expansion, thereby linking an altered electrophoretic mobility of the mutant protein to its abnormal function. Mutant huntingtin appeared in gray and white matter with no difference in expression in affected regions. The mutant protein was broader than the wild type and in 6 of 11 juvenile cases resolved as a complex of bands, consistent with evidence at the DNA level for somatic mosaicism. Thus, HD pathogenesis results from a gain of function by an aberrant protein that is widely expressed in brain and is harmful only to some neurons

    Identification and characterization of a novel non-structural protein of bluetongue virus

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    Bluetongue virus (BTV) is the causative agent of a major disease of livestock (bluetongue). For over two decades, it has been widely accepted that the 10 segments of the dsRNA genome of BTV encode for 7 structural and 3 non-structural proteins. The non-structural proteins (NS1, NS2, NS3/NS3a) play different key roles during the viral replication cycle. In this study we show that BTV expresses a fourth non-structural protein (that we designated NS4) encoded by an open reading frame in segment 9 overlapping the open reading frame encoding VP6. NS4 is 77–79 amino acid residues in length and highly conserved among several BTV serotypes/strains. NS4 was expressed early post-infection and localized in the nucleoli of BTV infected cells. By reverse genetics, we showed that NS4 is dispensable for BTV replication in vitro, both in mammalian and insect cells, and does not affect viral virulence in murine models of bluetongue infection. Interestingly, NS4 conferred a replication advantage to BTV-8, but not to BTV-1, in cells in an interferon (IFN)-induced antiviral state. However, the BTV-1 NS4 conferred a replication advantage both to a BTV-8 reassortant containing the entire segment 9 of BTV-1 and to a BTV-8 mutant with the NS4 identical to the homologous BTV-1 protein. Collectively, this study suggests that NS4 plays an important role in virus-host interaction and is one of the mechanisms played, at least by BTV-8, to counteract the antiviral response of the host. In addition, the distinct nucleolar localization of NS4, being expressed by a virus that replicates exclusively in the cytoplasm, offers new avenues to investigate the multiple roles played by the nucleolus in the biology of the cell
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