602 research outputs found

    Active noise control in finite length ducts

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    A simple technique for the active control of sound in ducts, initially suggested by Olson and May [1], is investigated in detail. A simple, "virtual earth" principle, feedback loop is used to drive the sound pressure to a minimum at a microphone placed close to a loudspeaker in the duct wall. This produces a reflection of downstream travelling plane waves. A detailed investigation of the loudspeaker near field has enabled the optimum position of the microphone to be identified. The system is shown to be especially effective at the frequencies of the longitudinal duct resonances, where the acoustic response of the duct produces a high loop gain. Results are presented which show a reduction of up to 20 dB in the amplitude of low frequency broadband noise at a position downstream of the cancelling source.</p

    A study of zinc transporter 1 and its role in Type 3 Haemochromatosis

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    Hereditary haemochromatosis is an autosomal recessive disorder of iron metabolism, characterised by increased iron absorption and progressive iron accumulation particularly in the liver. It has been shown that hepatocytes can acquire iron in two forms; transferrin-bound iron (TBI) and non-transferrin-bound iron (NTBI)1. Known transporters of NTBI into the cell include DMT1 and ZIP14, and FPN is the only transporter known to export iron. The aims of this study were to characterize the zinc transporter, ZnT-1 and determine whether it is involved in iron transport, specifically as an exporter. There was a decrease in mRNA expression of the short untranslated isoform of ZnT-1 in double mutant (Hfe -/- and TfR2 Y245X) mouse liver, a trend also seen in TfR1 and Hamp. The long untranslated isoform, however, was significantly higher in the iron-deficient mice as was expression of TfR1 and Ferroportin. Iron and zinc efflux was measured in cells over-expressing ZnT-1 and control cells. There was no difference between over-expressed and control cells in iron efflux. However, at 60 min, over-expressed cells had significantly more zinc efflux than control cells. More zinc than iron was released from the cell. The results of this study do not support the hypotheses that (i) ZnT-1 reduces intracellular cytoplasmic iron concentration by promoting efflux and 2 ZnT-1 is down-regulated in iron-loaded cells

    The Role of Fault in Separation and Divorce. Italian Law

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    The books collects essays from different legal systems. It results after a research on "The role of fault in divorce" funded by the Nuffield Foundation (U.K.

    Improving the network scalability of Erlang

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    As the number of cores grows in commodity architectures so does the like- lihood of failures. A distributed actor model potentially facilitates the de- velopment of reliable and scalable software on these architectures. Key com- ponents include lightweight processes which ‘share nothing’ and hence can fail independently. Erlang is not only increasingly widely used, but the un- derlying actor model has been a beacon for programming language design, influencing for example Scala, Clojure and Cloud Haskell. While the Erlang distributed actor model is inherently scalable, we demon- strate that it is limited by some pragmatic factors. We address two network scalability issues here: globally registered process names must be updated on every node (virtual machine) in the system, and any Erlang nodes that com- municate maintain an active connection. That is, there is a fully connected O(n^2) network of n nodes. We present the design, implementation, and initial evaluation of a con- servative extension of Erlang – Scalable Distributed (SD) Erlang. SD Erlang partitions the global namespace and connection network using s groups. An s group is a set of nodes with its own process namespace and with a fully connected network within the s group, but only individual connections out- side it. As a node may belong to more than one s group it is possible to construct arbitrary connection topologies like trees or rings

    Letting in the Trojan mouse: Using an eportfolio system to re-think pedagogy.

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    Copyright statement: Copyright 2008 Julie Hughes. The author assigns to ascilite and educational non-profit institutions a non-exclusive licence to use this document for personal use and in courses of instruction provided that the article is used in full and this copyright statement is reproduced. The author also grants a non-exclusive licence to ascilite to publish this document on the ascilite web site and in other formats for Proceedings ascilite Melbourne 2008. Any other use is prohibited without the express permission of the author.E-learning research, as an emergent field in the UK, is highly political in nature (Conole & Oliver, 2007, p.6) occupying a complex landscape which houses policy-makers, researchers and practitioners. Increasingly and more interestingly, the landscape is being shaped by the narratives and experiences of the learners themselves (Creanor et al., 2006, Conole et al., 2006) and the use of Web 2.0 technologies. However, as Laurillard (2007, p.xv) reminds us we still, ‘tend to use technology to support traditional modes of teaching’ and ‘we scarcely have the infrastructure, the training, the habits or the access to the new technology, to be optimising its use just yet’ (p.48). Web 2.0 spaces, literacies and practices offer the possibility for new models of education (Mayes & de Freitas, 2007, p.13) which support iterative and integrative learning but as educators and higher educational establishments are we prepared and ready to re-think our pedagogies and re-do (Beetham & Sharpe 2007, p.3) our practices? This concise paper will reflect upon how the use of new learning landscapes such as eportfolios might offer us the opportunity to reflect upon the implications of letting in the e-learning eportfolio Trojan mouse (Sharpe & Oliver, 2007, p.49)

    Our emblem [music] : (Australian national song) /

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    For voice and piano.; Caption title.; Cover bears ill. of a kangaroo and an emu on grass.; "J.R. Coxon, The 'Centreway' Geelong West"--At bottom of p. 2.; "The men who made our emblem ... a hundred years ago ..."--From the lyrics.; Publication date approximated from the lyrics and the existence of J.R. Coxon (from Victorian Heritage Database place details); Also available online http://nla.gov.au/nla.mus-vn5432352; From the collection of Keith Watson. ANL.Title from cover: Australian national song, entitled 'Our emblem' on the emu anc kangaroo. 'Neither goes backwards.' : advance Australi

    DETERMINAÇÃO DOS TEORES DE ÁCIDO ACETILSALICÍLICO EM AMOSTRAS DE PLASMA POR ESPECTROFOTOMETRIA Doi: http://dx.doi.org/10.5892/ruvrd.v11i2.239250

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    O monitoramento terapêutico constitui atividade sistemática de análise de fármacos e seus metabólitos ativos em material biológico, com o objetivo de se obter a máxima eficácia terapêutica com mínimo ou ausência de efeitos tóxicos. É recomendada para pacientes que usam Ácido Acetilsalicílico (AAS) de forma crônica, devido à alta variabilidade interindividual das concentrações plasmáticas e a baixa adesão de alguns pacientes. Assim, o objetivo deste trabalho foi o de determinar os teores de AAS em amostras de plasma, de pacientes em uso de ácido acetilsalicílico (100mg), atendidos no Programa de Saúde da Família (PSF 14) de Lavras – MG, visando monitorização terapêutica. Foram selecionados 10 pacientes, maiores de 18 anos e de ambos os sexos, sob uso de AAS 100 mg em diferentes regimes de dosagem. Essas amostras foram coletadas imediatamente antes da ingestão da próxima dose (concentração vale) e foram analisadas pelo método espectrofotométrico de Trinder, (λ 540nm). Para cálculo de teor de AAS em plasma utilizou-se a equação (y = 0,0197x + 0,0157), com um coeficiente de determinação (R2) de 0,9996. Foram encontrados valores entre 0,0 e 3,67mg%. Metade dos pacientes analisados, provavelmente, não estava aderindo ao tratamento ou ainda estavam em dose subterapêutica; o que pode ser justificado pela alta frequência com que são relatados os efeitos adversos. O método de Trinder é fácil, rápido e aplicável para prática clínica. Mas ainda é necessária a determinação de valores de referência específicos para a dosagem de AAS no plasma, quando este é administrado em baixas doses (efeito anticoagulante)
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