283 research outputs found

    Fuel Cell Testing Protocols: An International Perspective

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    An overview of international polymer-electrolyte fuel cell (PEMFC) test procedures is presented. This overview is the first step in the global harmonization of testing methods. Many techniques and procedures determining stack performance and durability are discussed. Each approach has differences that may or may not impact the data and data quality. Through experiments, it was found that differences in the results from two methods for measuring sequential polarization curves are minimal. Answers to questions regarding differences in the aging duty cycles need to be determined experimentally. The results of these experiments are expected to help the harmonization process, to facilitate the understanding of test results, and, possibly, to accelerate the commercialization of PEMFCs.JRC.F.2-Cleaner energ

    General Statistical properties of the CMB Polarization field

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    The distribution of the polarization of the Cosmic Microwave Background (CMB) in the sky is determined by the hypothesis of random Gaussian distribution of the primordial density perturbations. This hypotheses is well motivated by the inflationary cosmology. Therefore, the test of consistency of the statistical properties of the CMB polarization field with the Gaussianity of primordial density fluctuations is a realistic way to study the nature of primordial inhomogeneities in the Universe. This paper contains the theoretical predictions of the general statistical properties of the CMB polarization field. All results obtained under assumption of the Gaussian nature of the signal. We pay the special attention to the following two problems. First, the classification and statistics of the singular points of the polarization field where polarization is equal to zero. Second, the topology of contours of the value of the degree of polarization. We have investigated the percolation properties for the zones of ``strong'' and ``weak'' polarization. We also have calculated Minkowski functionals for the CMB polarization field. All results are analytical.Comment: Latex, 22 pages, including 5 figure

    World Antimalarial Resistance Network (WARN) II: In vitro antimalarial drug susceptibility

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    Intrinsic resistance of Plasmodium falciparum is clearly a major determinant of the clinical failure of antimalarial drugs. However, complex interactions between the host, the parasite and the drug obscure the ability to define parasite drug resistance in vivo. The in vitro antimalarial drug susceptibility assay determines ex-vivo growth of parasite in the presence of serial drug concentrations and, thus, eliminates host effects, such as drug metabolism and immunity. Although the sensitivity of the parasite to various antimalarials provided by such a test provides an important indicator of intrinsic parasite susceptibility, there are fundamental methodological issues that undermine comparison of in vitro susceptibility both between laboratories and within a single laboratory over time. A network of laboratories is proposed that will agree on the basic parameters of the in vitro test and associated measures of quality control. The aim of the network would be to establish baseline values of sensitivity to commonly used antimalarial agents from key regions of the world, and create a global database, linked to clinical, molecular and pharmacology databases, to support active surveillance to monitor temporal trends in parasite susceptibility. Such a network would facilitate the rapid detection of strains with novel antimalarial resistance profiles and investigate suitable alternative treatments with retained efficacy

    Tools and methods in participatory modeling: Selecting the right tool for the job

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    © 2018 Elsevier Ltd Various tools and methods are used in participatory modelling, at different stages of the process and for different purposes. The diversity of tools and methods can create challenges for stakeholders and modelers when selecting the ones most appropriate for their projects. We offer a systematic overview, assessment, and categorization of methods to assist modelers and stakeholders with their choices and decisions. Most available literature provides little justification or information on the reasons for the use of particular methods or tools in a given study. In most of the cases, it seems that the prior experience and skills of the modelers had a dominant effect on the selection of the methods used. While we have not found any real evidence of this approach being wrong, we do think that putting more thought into the method selection process and choosing the most appropriate method for the project can produce better results. Based on expert opinion and a survey of modelers engaged in participatory processes, we offer practical guidelines to improve decisions about method selection at different stages of the participatory modeling process

    Journalism, journalism education and a region's integration: The case of Southeast Asia

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    The 50-year-old Association of Southeast Asian Nations (ASEAN) is now in its third year implementing the mechanics of regional integration. How does this region-wide development affect journalism in individual countries and in the region? This qualitative research sought to find out the meaning and implications of regional integration to journalism practice and education in Southeast Asia. There is enthusiasm over developing a model on ‘ASEAN-centered journalism and journalism education’, however there are country-level realities that news organisations and journalism schools face before proceeding to even attuning reportage and journalism instruction to the needs of ASEAN

    Theoretical Studies of Spectroscopy and Dynamics of Hydrated Electrons.

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    Drug-resistant genotypes and multi-clonality in Plasmodium falciparum analysed by direct genome sequencing from peripheral blood of malaria patients.

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    Naturally acquired blood-stage infections of the malaria parasite Plasmodium falciparum typically harbour multiple haploid clones. The apparent number of clones observed in any single infection depends on the diversity of the polymorphic markers used for the analysis, and the relative abundance of rare clones, which frequently fail to be detected among PCR products derived from numerically dominant clones. However, minority clones are of clinical interest as they may harbour genes conferring drug resistance, leading to enhanced survival after treatment and the possibility of subsequent therapeutic failure. We deployed new generation sequencing to derive genome data for five non-propagated parasite isolates taken directly from 4 different patients treated for clinical malaria in a UK hospital. Analysis of depth of coverage and length of sequence intervals between paired reads identified both previously described and novel gene deletions and amplifications. Full-length sequence data was extracted for 6 loci considered to be under selection by antimalarial drugs, and both known and previously unknown amino acid substitutions were identified. Full mitochondrial genomes were extracted from the sequencing data for each isolate, and these are compared against a panel of polymorphic sites derived from published or unpublished but publicly available data. Finally, genome-wide analysis of clone multiplicity was performed, and the number of infecting parasite clones estimated for each isolate. Each patient harboured at least 3 clones of P. falciparum by this analysis, consistent with results obtained with conventional PCR analysis of polymorphic merozoite antigen loci. We conclude that genome sequencing of peripheral blood P. falciparum taken directly from malaria patients provides high quality data useful for drug resistance studies, genomic structural analyses and population genetics, and also robustly represents clonal multiplicity

    Drug resistance to sulphadoxine-pyrimethamine in Plasmodium falciparum malaria in Mlimba, Tanzania

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    BACKGROUND: Sulphadoxine-pyrimethamine (SP) has been and is currently used for treatment of uncomplicated Plasmodium falciparum malaria in many African countries. Nevertheless, the response of parasites to SP treatment has shown significant variation between individuals. METHODS: The genes for dihydrofolate reductase (dhfr) and dihydropteroate synthase (dhps) were used as markers, to investigate parasite resistance to SP in 141 children aged less than 5 years. Parasite DNA was extracted by Chelex method from blood samples collected and preserved on filter papers. Subsequently, polymerase chain reaction (PCR) and restriction fragment length polymorphism (PCR-RFLP) were applied to detect the SP resistance-associated point mutations on dhfr and dhps. Commonly reported point mutations at codons 51, 59, 108 and 164 in the dhfr and codons 437, 540 and 581 in the dhps domains were examined. RESULTS: Children infected with parasites harbouring a range of single to quintuple dhfr/dhps mutations were erratically cured with SP. However, the quintuple dhfr/dhps mutant genotypes were mostly associated with treatment failures. High proportion of SP resistance-associated point mutations was detected in this study but the adequate clinical response (89.4%) observed clinically at day 14 of follow up reflects the role of semi-immunity protection and parasite clearance in the population. CONCLUSION: In monitoring drug resistance to SP, concurrent studies on possible confounding factors pertaining to development of resistance in falciparum malaria should be considered. The SP resistance potential detected in this study, cautions on its useful therapeutic life as an interim first-line drug against malaria in Tanzania and other malaria-endemic countries
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