3,186 research outputs found

    A historical review of the development of electronic textiles

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    Textiles have been at the heart of human technological progress for thousands of years, with textile developments closely tied to key inventions that have shaped societies. The relatively recent invention of electronic textiles is set to push boundaries again and has already opened up the potential for garments relevant to defense, sports, medicine, and health monitoring. The aim of this review is to provide an overview of the key innovative pathways in the development of electronic textiles to date using sources available in the public domain regarding electronic textiles (E-textiles); this includes academic literature, commercialized products, and published patents. The literature shows that electronics can be integrated into textiles, where integration is achieved by either attaching the electronics onto the surface of a textile, electronics are added at the textile manufacturing stage, or electronics are incorporated at the yarn stage. Methods of integration can have an influence on the textiles properties such as the drapability of the textile

    An evaluation of element mobility in the Modderfontein ultramafic complex, Johannesburg: Origin as an Archaean ophiolite fragment or greenstone belt remnant?

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    This is the author accepted manuscript. The final version is available from the publisher via the DOI in this recordThe Johannesburg Dome – a tonalite-trondhjemite-granodiorite (TTG)-dominated terrane in the central Kaapvaal Craton – contains a suite of ultramafic-mafic complexes that are concentrated largely along its southern rim. These >3.3 Ga ultramafic-mafic complexes have recently been re-interpreted as fragments of an Archaean ophiolite (Anhaeusser 2006a), challenging a longstanding hypothesis whereby the complexes represent the intruded remnants of an Archaean greenstone belt. As with similar interpretations of ultramafic-mafic units in other Archaean cratons, the ophiolite hypothesis is used as evidence in favour of Phanerozoic-style plate tectonic processes having operated in the Archaean, with this geodynamic regime the prevailing explanation for the rocks and structures displayed by the Kaapvaal Craton. Through detailed new geological mapping of the scarcely studied Modderfontein Complex, alongside petrography, bulk-rock geochemistry and mineral chemistry, we here assess the validity of both hypotheses. Moreover, having experienced amphibolite-facies metamorphism and substantial hydrothermal alteration, we assess the degree of element mobility experienced by the Modderfontein Complex and discuss the implications for subsequent geodynamic interpretations. The 1 km2 area mapped comprises separate northern and southern domains, with the former dominated by homogenous serpentinite that contains irregularly-shaped chromitite lenses, and the latter comprising coarsely-layered peridotite, pyroxenite, gabbro and amphibolite. The data indicate that the Modderfontein Complex has experienced significant mobility of Pd, the fluid-mobile lithophile elements (e.g., Ba, Rb and Cs) and potentially some elements generally considered immobile. Mobility of Pd is restricted to chromitite lenses, where Pd was originally hosted by sulphide mineral phases (e.g., pentlandite). This element was immobile in all other Modderfontein lithologies, where it is hosted by nano-scale PGM, demonstrating that PGE mobility is, in-part, controlled by the host phase(s). Moreover, based on a variety of petrographic and geochemical characteristics, including PGE mineralogy and spinel mineral chemistry, it is considered unlikely that the Modderfontein Complex represents an ophiolite fragment. Instead, the Complex is interpreted as the intrusive remnant of a greenstone belt that was subsequently intruded by TTG magmas.Society of Economic GeologistsGeological Societ

    Many-body mobility edge due to symmetry-constrained dynamics and strong interactions

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    We provide numerical evidence combined with an analytical understanding of the many-body mobility edge for the strongly anisotropic spin-1/2 XXZ model in a random magnetic field. The system dynamics can be understood in terms of symmetry-constrained excitations about parent states with ferromagnetic and antiferromagnetic short range order. These two regimes yield vastly different dynamics producing an observable, tunable many-body mobility edge. We compute a set of diagnostic quantities that verify the presence of the mobility edge and discuss how weakly correlated disorder can tune the mobility edge further

    Determining the clog state of constructed wetlands using an embeddable Earth's Field Nuclear Magnetic Resonance probe

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    The recent rise in interest of green technologies has led to significant adoption of the constructed wetland as a waste water treatment technique. This increased popularity has only been mired by the decline in operational lifetime of wetland units, leading to the need for more regular, time consuming, and expensive rejuvenation techniques to be performed than initially anticipated. To extend operational lifetimes and increase efficiency of wetland units, it is crucial to have an accurate method to determine the internal state of the wetland system. The most important parameter to measure within the reed bed is the clog state of the system, which is representative of the overall system health. In previous work, magnetic resonance (MR) measurements, parameters of T1 and T2eff, have been demonstrated as extremely powerful tools to determine the internal clog state of a wetland [1, 2]. Measurements have been performed in a laboratory setting, using low field permanent magnet arrangements. This work presents an Earth's Field Nuclear Magnetic Resonance (EFNMR) probe suitable for in situ measurements within constructed wetlands. We show T2eff and T1 measurements using the EFNMR probe. T1 values are shown to be sensitive to the change in the clog state with 1498 ms for the thickly clogged sample and 2728 ms for the thinly clogged sample. T2eff values are shown to be marginally more sensitive to clog state with 630 ms for a thickly clogged sample and 1212 ms for the thinly clogged sample. This gives distinguishable variation within both parameters suggesting that this probe is suitable for embedding into an operational constructed wetland. This work was conducted as part of an EU FP7 project to construct an Automated Reed Bed Installation, "ARBI"

    TreeRipper web application: towards a fully automated optical tree recognition software

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    Background: Relationships between species, genes and genomes have been printed as trees for over a century. Whilst this may have been the best format for exchanging and sharing phylogenetic hypotheses during the 20(th) century, the worldwide web now provides faster and automated ways of transferring and sharing phylogenetic knowledge. However, novel software is needed to defrost these published phylogenies for the 21(st) century. Results: TreeRipper is a simple website for the fully-automated recognition of multifurcating phylogenetic trees (http://linnaeus.zoology.gla.ac.uk/similar to jhughes/treeripper/). The program accepts a range of input image formats (PNG, JPG/JPEG or GIF). The underlying command line c++ program follows a number of cleaning steps to detect lines, remove node labels, patch-up broken lines and corners and detect line edges. The edge contour is then determined to detect the branch length, tip label positions and the topology of the tree. Optical Character Recognition (OCR) is used to convert the tip labels into text with the freely available tesseract-ocr software. 32% of images meeting the prerequisites for TreeRipper were successfully recognised, the largest tree had 115 leaves. Conclusions: Despite the diversity of ways phylogenies have been illustrated making the design of a fully automated tree recognition software difficult, TreeRipper is a step towards automating the digitization of past phylogenies. We also provide a dataset of 100 tree images and associated tree files for training and/or benchmarking future software. TreeRipper is an open source project licensed under the GNU General Public Licence v

    The PD COMM trial: A protocol for the process evaluation of a randomised trial assessing the effectiveness of two types of SLT for people with Parkinson's disease

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    BACKGROUND: The PD COMM trial is a phase III multi-centre randomised controlled trial whose aim is to evaluate the effectiveness and cost-effectiveness of two approaches to speech and language therapy (SLT) compared with no SLT intervention (control) for people with Parkinson's disease who have self-reported or carer-reported problems with their speech or voice. Our protocol describes the process evaluation embedded within the outcome evaluation whose aim is to evaluate what happened at the time of the PD COMM intervention implementation and to provide findings that will assist in the interpretation of the PD COMM trial results. Furthermore, the aim of the PD COMM process evaluation is to investigate intervention complexity within a theoretical model of how the trialled interventions might work best and why. METHODS/DESIGN: Drawing from the Normalization Process Theory and frameworks for implementation fidelity, a mixed method design will be used to address process evaluation research questions. Therapists' and participants' perceptions and experiences will be investigated via in-depth interviews. Critical incident reports, baseline survey data from therapists, treatment record forms and home practice diaries also will be collected at relevant time points throughout the running of the PD COMM trial. Process evaluation data will be analysed independently of the outcome evaluation before the two sets of data are then combined. DISCUSSION: To date, there are a limited number of published process evaluation protocols, and few are linked to trials investigating rehabilitation therapies. Providing a strong theoretical framework underpinning design choices and being tailored to meet the complex characteristics of the trialled interventions, our process evaluation has the potential to provide valuable insight into which components of the interventions being delivered in PD COMM worked best (and what did not), how they worked well and why

    Social preference weights for treatments in Fabry disease in the UK : a discrete choice experiment

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    Abstract Objective: Fabry disease is a rare inherited lysosomal storage disorder caused by deficiency of α-galactosidase A. Effective enzyme replacement therapies are available that are administered intravenously. However, a new oral treatment is being developed as an alternative option for patients with amenable mutations. This study was designed to understand the value that people place on the different features of treatments for Fabry disease. Research design and methods: A discrete choice experiment (DCE) was designed to assess the importance of different aspects of treatments for Fabry disease. The attributes included overall survival, mode of administration, treatment related reactions, treatment related headaches and risk of antibody formation. Attributes were combined using a published orthogonal array into choice sets. A research panel was used to survey the UK general public. The mixed logit model was used to estimate strength of preference for the attributes and marginal rates of substitution (MRSs). Disutilities were estimated from the DCE data for changes in each attribute. Results: The sample (n = 506) was broadly representative of UK demographics. The logit model revealed that all attributes were significant predictors of choice. Participants were significantly more likely to choose a treatment which meant an increase in their life expectancy by 1 year (odds ratio = 1.574; 95% CI = 1.504–1.647) and significantly less likely to choose self-administered intravenous (IV) treatment compared to an every other day tablet (OR = 0.426 95% CI = 0.384–0.474). Estimated disutilities were −0.0543 (self-administered infusion), treatment related headaches 12 times a year (−0.0361) and infusion reactions six times a year (−0.0202). Conclusions: The survey revealed a significant preference for oral treatment compared with IV even in the context of a treatment that can extend overall survival. MRSs were used as a basis for estimating disutilities associated with changes in attribute levels which could be used to weight QALYs. It is possible that other important treatment attributes are missing from this research which may have provided further insights. It would also be useful to extend this research to include Fabry disease patients so their preferences can be assessed against the societal perspective

    Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency

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    This work has been supported by the Medical Research Council UK (New Investigator Research Grant G0801265 to L.A.M., Clinical Research Training Fellowship Grant G0901980 to C.R.H. and Project Grant G0700767 to P.J.K.)
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