230 research outputs found

    Origin and age of an ongoing radioactive contamination of soils near La hague reprocessing plant based on <sup>239+240</sup>Pu/<sup>238</sup>Pu and <sup>241</sup>Am/<sup>241</sup>Pu current ratios and <sup>90</sup>Sr and Ln(III) soil contents.

    Get PDF
    Nuclear reprocessing plants are sources of environmental contamination by gaseous or liquid discharges. Numerous radionuclides are of concern, with actinides and &lt;sup&gt;90&lt;/sup&gt; Sr being the most radiotoxic. Environmental radioactivity survey programs mostly use γ-spectrometry to track contaminations because γ-spectrometry is very cost effective and can be carried out on raw samples. On the other hand, the determination of β- or α-emitting radionuclides in environmental samples requires rather sophisticated analytical methods, and are thus dedicated to specific goals. However, measuring radionuclides such as Pu, Am, and Sr often provides more information about the presence of a current or prior contamination and on its origin, based on the isotopic composition of the samples. We found that the analysis of &lt;sup&gt;241&lt;/sup&gt; Pu, &lt;sup&gt;239+240&lt;/sup&gt; Pu, &lt;sup&gt;241&lt;/sup&gt; Am, and &lt;sup&gt;90&lt;/sup&gt; Sr of a few selected soil samples taken near the nuclear reprocessing plant of La Hague, France, revealed the presence of a previous environmental contamination originating from several incidents in La Hague site involving atmospheric transfer and leaks in flooded waste pits. The &lt;sup&gt;241&lt;/sup&gt; Am- &lt;sup&gt;241&lt;/sup&gt; Pu dating method indicated a contamination period prior to 1983. The presence of elevated levels of light non-radioactive lanthanides and yttrium in the soil samples confirmed the involvement of cold fuel. Our results demonstrate how long-lived actinides are likely to reveal a long-term contamination of the environment by spent fuel. Our study indicates that there is a requirement to use more sophisticated tools than γ-spectrometry when surveying the environments surrounding industrial plants for nuclear power and nuclear reprocessing with a potential for the accidental release of radioactivity into the environment

    A cryogenic liquid-mirror telescope on the moon to study the early universe

    Full text link
    We have studied the feasibility and scientific potential of zenith observing liquid mirror telescopes having 20 to 100 m diameters located on the moon. They would carry out deep infrared surveys to study the distant universe and follow up discoveries made with the 6 m James Webb Space Telescope (JWST), with more detailed images and spectroscopic studies. They could detect objects 100 times fainter than JWST, observing the first, high-red shift stars in the early universe and their assembly into galaxies. We explored the scientific opportunities, key technologies and optimum location of such telescopes. We have demonstrated critical technologies. For example, the primary mirror would necessitate a high-reflectivity liquid that does not evaporate in the lunar vacuum and remains liquid at less than 100K: We have made a crucial demonstration by successfully coating an ionic liquid that has negligible vapor pressure. We also successfully experimented with a liquid mirror spinning on a superconducting bearing, as will be needed for the cryogenic, vacuum environment of the telescope. We have investigated issues related to lunar locations, concluding that locations within a few km of a pole are ideal for deep sky cover and long integration times. We have located ridges and crater rims within 0.5 degrees of the North Pole that are illuminated for at least some sun angles during lunar winter, providing power and temperature control. We also have identified potential problems, like lunar dust. Issues raised by our preliminary study demand additional in-depth analyses. These issues must be fully examined as part of a scientific debate we hope to start with the present article.Comment: 35 pages, 11 figures. To appear in Astrophysical Journal June 20 200

    Cost-effectiveness of HBV and HCV screening strategies:a systematic review of existing modelling techniques

    Get PDF
    Introduction: Studies evaluating the cost-effectiveness of screening for Hepatitis B Virus (HBV) and Hepatitis C Virus (HCV) are generally heterogeneous in terms of risk groups, settings, screening intervention, outcomes and the economic modelling framework. It is therefore difficult to compare cost-effectiveness results between studies. This systematic review aims to summarise and critically assess existing economic models for HBV and HCV in order to identify the main methodological differences in modelling approaches. Methods: A structured search strategy was developed and a systematic review carried out. A critical assessment of the decision-analytic models was carried out according to the guidelines and framework developed for assessment of decision-analytic models in Health Technology Assessment of health care interventions. Results: The overall approach to analysing the cost-effectiveness of screening strategies was found to be broadly consistent for HBV and HCV. However, modelling parameters and related structure differed between models, producing different results. More recent publications performed better against a performance matrix, evaluating model components and methodology. Conclusion: When assessing screening strategies for HBV and HCV infection, the focus should be on more recent studies, which applied the latest treatment regimes, test methods and had better and more complete data on which to base their models. In addition to parameter selection and associated assumptions, careful consideration of dynamic versus static modelling is recommended. Future research may want to focus on these methodological issues. In addition, the ability to evaluate screening strategies for multiple infectious diseases, (HCV and HIV at the same time) might prove important for decision makers

    Chronic Eczematous Eruptions of the Elderly Are Associated with Chronic Exposure to Calcium Channel Blockers: Results from a Case–Control Study

    Get PDF
    It has been suggested that chronic eczematous eruptions of the elderly could be associated with chronic drug exposure. To determine the drugs associated with these eruptions, we conducted a case–control study on 102 cases and 204 controls. Cases were consecutive patients older than 60 years presenting with an eczematous eruption that had evolved continuously or recurrently for more than 3 months without a reliable cause. Two controls were matched to each case on age, sex, in/outpatient origin, and center. Information about drug exposure was obtained from patients and their pharmacists. Drug use for more than 3 months within the year preceding the eruption was compared between cases and controls. An association was found between calcium channel blockers (CCB) and eczema, with a matched OR (odds ratio) of 2.5 (95% CI (confidence interval): 1.3–4.6). To ascertain the course of patients after CCB withdrawal, two ancillary studies were performed on 74 patients with eczematous eruptions from our department before the case–control study period, and on 101 patients registered in the French “Pharmacovigilance” database. Healing of these eruptions after CCB withdrawal occurred in 83 and 68% of these cases, respectively. The long-term use of CCB is a risk factor for chronic eczematous eruptions of the elderly

    Individual influenza A virus mRNAs show differential dependence on cellular NXF1/TAP for their nuclear export

    Get PDF
    The influenza A virus RNA-dependent RNA polymerase produces capped and polyadenylated mRNAs in the nucleus of infected cells that resemble mature cellular mRNAs, but are made by very different mechanisms. Furthermore, only two of the 10 viral protein-coding mRNAs are spliced: most are intronless, while two contain unremoved introns. The mechanism(s) by which any of these mRNAs are exported from the nucleus is uncertain. To probe the involvement of the primary cellular mRNA export pathway, we treated cells with siRNAs against NXF1, Aly or UAP56, or with the drug 5,6-dichloro-1-β-d-ribofuranosyl-benzimidazole (DRB), an inhibitor of RNA polymerase II phosphorylation previously shown to inhibit nuclear export of cellular mRNA as well as influenza virus segment 7 mRNAs. Depletion of NXF1 or DRB treatment had similar effects, inhibiting the nuclear export of several of the viral mRNAs. However, differing degrees of sensitivity were seen, depending on the particular segment examined. Intronless HA mRNA and spliced M2 or unspliced M1 transcripts (all encoding late proteins) showed a strong requirement for NXF1, while intronless early gene mRNAs, especially NP mRNA, showed the least dependency. Depletion of Aly had little effect on viral mRNA export, but reduction of UAP56 levels strongly inhibited trafficking and/or translation of the M1, M2 and NS1 mRNAs. Synthesis of NS2 from the spliced segment 8 transcript was, however, resistant. We conclude that influenza A virus co-opts the main cellular mRNA export pathway for a subset of its mRNAs, including most but not all late gene transcripts
    corecore