92 research outputs found

    Electroosmotically generated disinfectant from urine as a by-product of electricity in microbial fuel cell for the inactivation of pathogenic species

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    This work presents a small scale and low cost ceramic based microbial fuel cell, utilising human urine into electricity, while producing clean catholyte into an initially empty cathode chamber through the process of electro-osmostic drag. It is the first time that the catholyte obtained as a by-product of electricity generation from urine was transparent in colour and reached pH>13 with high ionic conductivity values. The catholyte was collected and used ex situ as a killing agent for the inactivation of a pathogenic species such as Salmonella typhimurium, using a luminometer assay. Results showed that the catholyte solutions were efficacious in the inactivation of the pathogen organism even when diluted up to 1:10, resulting in more than 5 log-fold reduction in 4 min. Long-term impact of the catholyte on the pathogen killing was evaluated by plating Salmonella typhimurium on agar plates and showed that the catholyte possesses a long-term killing efficacy and continued to inhibit pathogen growth for 10 days

    Missing Data in Sea Turtle Population Monitoring: A Bayesian Statistical Framework Accounting for Incomplete Sampling

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    This is the final version. Available on open access from Frontiers Media via the DOI in this recordData Availability Statement: Raw nest beach monitoring data gathered at sites outside of the national park will be made available upon request to the board of Renatura Congo ([email protected]). Raw nest beach monitoring data gathered at sites inside Conkouati-Douli National Park and code to run models are available from the Dryad Digital Repository: doi:10.5061/dryad.prr4xgxp3Monitoring how populations respond to sustained conservation measures is essential to detect changes in their population status and determine the effectiveness of any interventions. In the case of sea turtles, their populations are difficult to assess because of their complicated life histories. Ground-derived clutch counts are most often used as an index of population size for sea turtles; however, data are often incomplete with varying sampling intensity within and among sites and seasons. To address these issues, we: (1) develop a Bayesian statistical modelling framework that can be used to account for sampling uncertainties in a robust probabilistic manner within a given site and season; and (2) apply this to a previously unpublished long-term sea turtle dataset (n = 17 years) collated for the Republic of the Congo, which hosts two sympatrically nesting species of sea turtle (leatherback turtle [Dermochelys coriacea] and olive ridley turtle [Lepidochelys olivacea]). The results of this analysis suggest that leatherback turtle nesting levels dropped initially and then settled into quasi-cyclical levels of interannual variability, with an average of 573 (mean, 95% prediction interval: 554–626) clutches laid annually between 2012 and 2017. In contrast, nesting abundance for olive ridley turtles has increased more recently, with an average of 1,087 (mean, 95% prediction interval: 1,057–1,153) clutches laid annually between 2012 and 2017. These findings highlight the regional and global importance of this rookery with the Republic of the Congo, hosting the second largest documented populations of olive ridley and the third largest for leatherback turtles in Central Africa; and the fourth largest non-arribada olive ridley rookery globally. Furthermore, whilst the results show that Congo’s single marine and coastal national park provides protection for over half of sea turtle clutches laid in the country, there is scope for further protection along the coast. Although large parts of the African coastline remain to be adequately monitored, the modelling approach used here will be invaluable to inform future status assessments for sea turtles given that most datasets are temporally and spatially fragmented.Darwin InitiativeDepartment for Environment, Food and Rural Affairs (Defra)Research Englan

    An assessment of monitoring requirements and costs of 'Reduced Emissions from Deforestation and Degradation'

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    <p>Abstract</p> <p>Background</p> <p>Negotiations on a future climate policy framework addressing Reduced Emissions from Deforestation and Degradation (REDD) are ongoing. Regardless of how such a framework will be designed, many technical solutions of estimating forest cover and forest carbon stock change exist to support policy in monitoring and accounting. These technologies typically combine remotely sensed data with ground-based inventories. In this article we assess the costs of monitoring REDD based on available technologies and requirements associated with key elements of REDD policy.</p> <p>Results</p> <p>We find that the design of a REDD policy framework (and specifically its rules) can have a significant impact on monitoring costs. Costs may vary from 0.5 to 550 US$ per square kilometre depending on the required precision of carbon stock and area change detection. Moreover, they follow economies of scale, i.e. single country or project solutions will face relatively higher monitoring costs.</p> <p>Conclusion</p> <p>Although monitoring costs are relatively small compared to other cost items within a REDD system, they should be shared not only among countries but also among sectors, because an integrated monitoring system would have multiple benefits for non-REDD management. Overcoming initialization costs and unequal access to monitoring technologies is crucial for implementation of an integrated monitoring system, and demands for international cooperation.</p

    Observation of B(s)0→J/ψpp¯ decays and precision measurements of the B(s)0 masses

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    The first observation of the decays B 0 ( s ) → J / ψ p ¯ p is reported, using proton-proton collision data corresponding to an integrated luminosity of 5.2     fb − 1 , collected with the LHCb detector. These decays are suppressed due to limited available phase space, as well as due to Okubo-Zweig-Iizuka or Cabibbo suppression. The measured branching fractions are B ( B 0 → J / ψ p ¯ p ) = [ 4.51 ± 0.40 ( stat ) ± 0.44 ( syst ) ] × 10 − 7 , B ( B 0 s → J / ψ p ¯ p ) = [ 3.58 ± 0.19 ( stat ) ± 0.39 ( syst ) ] × 10 − 6 . For the B 0 s meson, the result is much higher than the expected value of O ( 10 − 9 ) . The small available phase space in these decays also allows for the most precise single measurement of both the B 0 mass as 5279.74 ± 0.30 ( stat ) ± 0.10 ( syst )     MeV and the B 0 s mass as 5366.85 ± 0.19 ( stat ) ± 0.13 ( syst )     MeV

    Transgenic mouse models for ADHD

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    Guidelines for management of ischaemic stroke and transient ischaemic attack 2008

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    This article represents the update of the European Stroke Initiative Recommendations for Stroke Management. These guidelines cover both ischaemic stroke and transient ischaemic attacks, which are now considered to be a single entity. The article covers referral and emergency management, Stroke Unit service, diagnostics, primary and secondary prevention, general stroke treatment, specific treatment including acute management, management of complications, and rehabilitation

    Amplitude analysis of the B0 (s)! K0K0 decays and measurement of the branching fraction of the B0! K0K0 decay

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    The B0→K∗0K‾∗0B^0 \to K^{*0} \overline{K}^{*0} and Bs0→K∗0K‾∗0B^0_s \to K^{*0} \overline{K}^{*0} decays are studied using proton-proton collision data corresponding to an integrated luminosity of 3fb−1^{-1}. An untagged and time-integrated amplitude analysis of B(s)0→(K+π−)(K−π+)B^0_{(s)} \to (K^+\pi^-)(K^-\pi^+) decays in two-body invariant mass regions of 150 MeV/c2/c^2 around the K∗0K^{*0} mass is performed. A stronger longitudinal polarisation fraction in the B0→K∗0K‾∗0{B^0 \to K^{*0} \overline{K}^{*0}} decay, fL=0.724±0.051 (stat)±0.016 (syst){f_L = 0.724 \pm 0.051 \,({\rm stat}) \pm 0.016 \,({\rm syst})}, is observed as compared to fL=0.240±0.031 (stat)±0.025 (syst){f_L = 0.240 \pm 0.031 \,({\rm stat}) \pm 0.025 \,({\rm syst})} in the Bs0→K∗0K‾∗0{B^0_s\to K^{*0} \overline{K}^{*0}} decay. The ratio of branching fractions of the two decays is measured and used to determine B(B0→K∗0K‾∗0)=(8.0±0.9 (stat)±0.4 (syst))×10−7\mathcal{B}(B^0 \to K^{*0} \overline{K}^{*0}) = (8.0 \pm 0.9 \,({\rm stat}) \pm 0.4 \,({\rm syst})) \times 10^{-7}.Comment: All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2019-004.html (LHCb public pages

    Search for Lepton-Universality Violation in B^{+}→K^{+}ℓ^{+}ℓ^{-} Decays.

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    A measurement of the ratio of branching fractions of the decays B^{+}→K^{+}μ^{+}μ^{-} and B^{+}→K^{+}e^{+}e^{-} is presented. The proton-proton collision data used correspond to an integrated luminosity of 5.0  fb^{-1} recorded with the LHCb experiment at center-of-mass energies of 7, 8, and 13 TeV. For the dilepton mass-squared range 1.1<q^{2}<6.0  GeV^{2}/c^{4} the ratio of branching fractions is measured to be R_{K}=0.846_{-0.054}^{+0.060}_{-0.014}^{+0.016}, where the first uncertainty is statistical and the second systematic. This is the most precise measurement of R_{K} to date and is compatible with the standard model at the level of 2.5 standard deviations

    Amplitude analysis of B-s(0) -> K-S(0) K-+/-pi(-/+) decays

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    The first untagged decay-time-integrated amplitude analysis of Bs0→KS0K±π∓B^{0}_{s} \rightarrow K^{0}_{\textrm{S}} K^{\pm}\pi^{\mp} decays is performed using a sample corresponding to 3.0 3.0\,fb−1^{-1} of pppp collision data recorded with the LHCb detector during 2011 and 2012. The data are described with an amplitude model that contains contributions from the intermediate resonances K∗(892)0,+K^{*}(892)^{0,+}, K2∗(1430)0,+K^*_2(1430)^{0,+} and K0∗(1430)0,+K^*_0(1430)^{0,+}, and their charge conjugates. Measurements of the branching fractions of the decay modes Bs0→K∗(892)±K∓B^{0}_{s} \rightarrow K^{*}(892)^{\pm}K^{\mp} and Bs0→K∗(892)0K‾0,K‾∗(892)0K0B^{0}_{s} \rightarrow K^{*}(892)^{0}\kern 0.2em\overline{\kern -0.2em K}{}^{0}, \kern 0.2em\overline{\kern -0.2em K}{}^{*}(892)^{0}K^{0} are in agreement with, and more precise than, previous results. The decays Bs0→K0∗(1430)±K∓B^{0}_{s} \rightarrow K^*_0(1430)^{\pm} K^{\mp} and Bs0→K0∗(1430)0K‾0,K‾0∗(1430)0K0B^{0}_{s} \rightarrow K^{*}_{0}(1430)^{0}\kern 0.2em\overline{\kern -0.2em K}{}^{0}, \kern 0.2em\overline{\kern -0.2em K}{}^{*}_{0}(1430)^{0}K^{0} are observed for the first time, each with significance over 10 standard deviations.Comment: 27 pages, 14 figures. All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2018-045.htm

    Search for Lepton-Universality Violation in B + → K + ℓ + ℓ − Decays

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    A measurement of the ratio of branching fractions of the decays B + → K + μ + μ − and B + → K + e + e − is presented. The proton-proton collision data used correspond to an integrated luminosity of 5.0     fb − 1 recorded with the LHCb experiment at center-of-mass energies of 7, 8, and 13 TeV. For the dilepton mass-squared range 1.1 < q 2 < 6.0     GeV 2 / c 4 the ratio of branching fractions is measured to be R K = 0.84 6 + 0.060 − 0.054 + 0.016 − 0.014 , where the first uncertainty is statistical and the second systematic. This is the most precise measurement of R K to date and is compatible with the standard model at the level of 2.5 standard deviations
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