10 research outputs found

    An intercomparison of procedures for the determination of total mercury in seawater and recommendations regarding mercury speciation during GEOTRACES cruises

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    Author Posting. © Association for the Sciences of Limnology and Oceanography, 2012. This article is posted here by permission of Association for the Sciences of Limnology and Oceanography for personal use, not for redistribution. The definitive version was published in Limnology and Oceanography: Methods 10 (2012): 90-100, doi:10.4319/lom.2012.10.90.We conducted a laboratory intercomparison of total mercury (Hg) determination in seawater collected during U.S. GEOTRACES Intercalibration cruises in 2008 and 2009 to the NW Atlantic and NE Pacific Oceans. Results indicated substantial disagreement between the participating laboratories, which appeared to be affected most strongly by bottle cleanliness and preservation procedures. In addition, we examined the effectiveness of various collection and sample preparation procedures that may be used on future GEOTRACES cruises. The type of sampling system and filtration medium appeared to make little difference to results. Finally, and in light of results from experiments that considered sample bottle material effect and the development of new methods for CH3Hg+ extraction from seawater, we propose a recommended procedure for determining all four of the major Hg species in seawater (elemental, dimethyl-, monomethyl-, and total Hg).This work was supported by the National Science Foundation program in Chemical Oceanography under grants OCE–0825157, –0825108, –0825583 and –0825068

    Methods for the sampling and analysis of marine aerosols: results from the 2008 GEOTRACES aerosol intercalibration experiment

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    Atmospheric deposition of trace elements and isotopes (TEI) is an important source of trace metals to the open ocean, impacting TEI budgets and distributions, stimulating oceanic primary productivity, and influencing biological community structure and function. Thus, accurate sampling of aerosol TEIs is a vital component of ongoing GEOTRACES cruises, and standardized aerosol TEI sampling and analysis procedures allow the comparison of data from different sites and investigators. Here, we report the results of an aerosol analysis intercalibration study by seventeen laboratories for select GEOTRACES-relevant aerosol species (Al, Fe, Ti, V, Zn, Pb, Hg, NO3-, and SO42-) for samples collected in September 2008. The collection equipment and filter substrates are appropriate for the GEOTRACES program, as evidenced by low blanks and detection limits relative to analyte concentrations. Analysis of bulk aerosol sample replicates were in better agreement when the processing protocol was constrained (+/- 9% RSD or better on replicate analyses by a single lab, n = 7) than when it was not (generally 20% RSD or worse among laboratories using different methodologies), suggesting that the observed variability was mainly due to methodological differences rather than sample heterogeneity. Much greater variability was observed for fractional solubility of aerosol trace elements and major anions, due to differing extraction methods. Accuracy is difficult to establish without an SRM representative of aerosols, and we are developing an SRM for this purpose. Based on these findings, we provide recommendations for the GEOTRACES program to and macro-nutrients to the open ocean (Okin et al. 2011) and is a key component of the international GEOTRACES program (GEOTRACES Planning Group 2006). A priority of the GEOTRACES program is to quantify both major and trace elements (e. g., Al, Fe, Ti, V, Zn, Pb, and Hg) and species such as nitrate and sulfate in marine aerosols. Therefore, marine aerosol samples collected during GEOTRACES cruises must follow sampling protocols that permit the collection and analysis of as many elements and compounds as possible, while meeting the constraints associated with basin-wide oceanographic cruises (e. g., space limitations, high-frequency sampling, etc.)

    An assessment of participatory integrated vector management for malaria control in Kenya

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    BACKGROUND : The World Health Organization (WHO) recommends integrated vector management (IVM) as a strategy to improve and sustain malaria vector control. However, this approach has not been widely adopted. OBJECTIVES : We comprehensively assessed experiences and findings on IVM in Kenya with a view to sharing lessons that might promote its wider application. METHODS : The assessment used information from a qualitative external evaluation of two malaria IVM projects implemented between 2006 and 2011 and an analysis of their accumulated entomological and malaria case data. The project sites were Malindi and Nyabondo, located in coastal and western Kenya, respectively. The assessment focused on implementation of five key elements of IVM: integration of vector control methods, evidence-based decision making, intersectoral collaboration, advocacy and social mobilization, and capacity building. RESULTS : IVM was more successfully implemented in Malindi than in Nyabondo owing to greater community participation and multistakeholder engagement. There was a significant decline in the proportion of malaria cases among children admitted to Malindi Hospital, from 23.7% in 2006 to 10.47% in 2011 (p < 0.001). However, the projects’ operational research methodology did not allow statistical attribution of the decline in malaria and malaria vectors to specific IVM interventions or other factors. CONCLUSIONS : Sustaining IVM is likely to require strong participation and support from multiple actors, including community-based groups, non-governmental organizations, international and national research institutes, and various government ministries. A cluster-randomized controlled trial would be essential to quantify the effectiveness and impact of specific IVM interventions, alone or in combination.Grants from the Biovision Foundation (Switzerland) through the International Centre of Insect Physiology and Ecology (ICIPE).http://ehp.niehs.nih.govam2016School of Health Systems and Public Health (SHSPH

    Chemical Processes Influencing Mercury Transformations And Atmospheric Fluxes In The Atmospheric Boundary Layer In Coastal Regions

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    The atmosphere has been recognized as the major contributor of mercury inputs to terrestrial and aquatic environments. While considerable research on atmospheric concentrations and fluxes of Hg has been carried out in the Northern Hemisphere, this is not the case for the Southern hemisphere, remote islands and parts of the open ocean. In this work, atmospheric Hg concentrations and fluxes were determined for locations in South Africa and Bermuda. The concentrations of Hg and other trace metals (Al, Fe, Mn, Co, Ni, Cu, Zn, Cd and Pb) in precipitation are presented for Pretoria, an urban center and Cape Point, a Global Atmospheric Watch (G.A.W.) site in a nature reserve in South Africa. For Bermuda, Hg concentrations in air, precipitation and particles and deposition fluxes were determined. While these places have distinct differences, these results demonstrate that these locations share similarities in terms of the factors and atmospheric processes that influence deposition. Further, at both locations atmospheric Hg inputs pose a threat to coastal ecosystems, and chemical reactions in the atmosphere enhance the production of reactive gaseous Hg (RGHg) species, which is readily deposited. Additionally, ancillary data and atmospheric back-trajectories help to determine potential sources. Associations between Hg and other trace metals and concentrations of radon (222Rn) and carbon monoxide (CO) help to determine the relative strength of anthropogenic influences at the South African sites. The role of particles and chemical processes that enhance inputs to the coastal ecosystem in Bermuda are discussed, Finally, the importance of sampling and analytical methods & procedures in Hg research and indeed all trace metal research is demonstrated through participation in an international inter-comparison exercise under the GEOTRACES program

    Mobile atmospheric measurements and local-scale inverse estimation of the location and rates of brief CH<sub>4</sub> and CO<sub>2</sub> releases from point sources

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    International audienceWe present a local-scale atmospheric inversion framework to estimate the location and rate of methane (CH4) and carbon dioxide (CO2) releases from point sources. It relies on mobile near-ground atmospheric CH4 and CO2 mole fraction measurements across the corresponding atmospheric plumes downwind of these sources, on high-frequency meteorological measurements, and on a Gaussian plume dispersion model. The framework exploits the scatter of the positions of the individual plume cross sections, the integrals of the gas mole fractions above the background within these plume cross sections, and the variations of these integrals from one cross section to the other to infer the position and rate of the releases. It has been developed and applied to provide estimates of brief controlled CH4 and CO2 point source releases during a 1-week campaign in October 2018 at the TOTAL experimental platform TADI in Lacq, France. These releases typically lasted 4 to 8 min and covered a wide range of rates (0.3 to 200 g CH4/s and 0.2 to 150 g CO2/s) to test the capability of atmospheric monitoring systems to react fast to emergency situations in industrial facilities. It also allowed testing of their capability to provide precise emission estimates for the application of climate change mitigation strategies. However, the low and highly varying wind conditions during the releases added difficulties to the challenge of characterizing the atmospheric transport over the very short duration of the releases. We present our series of CH4 and CO2 mole fraction measurements using instruments on board a car that drove along roads ∼50 to 150 m downwind of the 40 m × 60 m area for controlled releases along with the estimates of the release locations and rates. The comparisons of these results to the actual position and rate of the controlled releases indicate ∼10 %–40 % average errors (depending on the inversion configuration or on the series of tests) in the estimates of the release rates and ∼30–40 m errors in the estimates of the release locations. These results are shown to be promising, especially since better results could be expected for longer releases and under meteorological conditions more favorable to local-scale dispersion modeling. However, the analysis also highlights the need for methodological improvements to increase the skill for estimating the source locations

    Near‐field atmospheric inversions for the localization and quantification of controlled methane releases using stationary and mobile measurements

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    International audienceThis study evaluates two local-scale atmospheric inversion approaches for the monitoring of methane (CH 4) emissions from industrial sites based on in situ atmospheric CH 4 mole fraction measurements from stationary or mobile sensors. We participated in a two-week campaign of CH 4 controlled-release experiments at TotalEnergies Anomaly Detection Initiatives (TADI) in Lacq, France in October 2019. We analyzed releases from various points within a 40 m × 50 m area with constant rates of 0.16 to 30 g CH 4 s −1 over 25 to 75 mins, using fixed-point and mobile measurements, and testing different inversion configurations with a Gaussian dispersion model. An inlet switching system, combining a limited number (6-7) of high-precision gas analyzers with a higher number (16) of sampling lines, ensured that a sufficient number of fixed measurement points sampled the plume downwind of the sources and the background mole fractions for any wind direction. The inversions using these fixed-point measurements provide release rate estimates with approximately 23%-30% average errors and estimates of the location of the releases with approximately 8-10 m average errors. The inversions using the mobile measurements provide estimates with approximately 20%-30% average errors for the release rates and approximately 30 m average errors for the release locations. The precision of the release rate estimates from both inversion frameworks corresponds to the best estimation This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes

    Pooled testing conserves SARS-CoV-2 laboratory resources and improves test turn-around time: Experience on the Kenyan Coast

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    Background: International recommendations for the control of the coronavirus disease 2019 (COVID-19) pandemic emphasize the central role of laboratory testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the etiological agent, at scale. The availability of testing reagents, laboratory equipment and qualified staff are important bottlenecks to achieving this. Elsewhere, pooled testing (i.e. combining multiple samples in the same reaction) has been suggested to increase testing capacities in the pandemic period. Methods: We discuss our experience with SARS-CoV-2 pooled testing using real-time reverse transcription polymerase chain reaction (RT-PCR) on the Kenyan Coast. Results: In mid-May, 2020, our RT-PCR testing capacity for SARS-CoV-2 was improved by ~100% as a result of adoption of a six-sample pooled testing strategy. This was accompanied with a concomitant saving of ~50% of SARS-CoV-2 laboratory test kits at both the RNA extraction and RT-PCR stages. However, pooled testing came with a slight decline of test sensitivity. The RT-PCR cycle threshold value (ΔCt) was ~1.59 higher for samples tested in pools compared to samples tested singly. Conclusions: Pooled testing is a useful strategy to increase SARS-CoV-2 laboratory testing capacity especially in low-income settings

    A systematic global stocktake of evidence on human adaptation to climate change

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    Assessing global progress on human adaptation to climate change is an urgent priority. Although the literature on adaptation to climate change is rapidly expanding, little is known about the actual extent of implementation. We systematically screened >48,000 articles using machine learning methods and a global network of 126 researchers. Our synthesis of the resulting 1,682 articles presents a systematic and comprehensive global stocktake of implemented human adaptation to climate change. Documented adaptations were largely fragmented, local and incremental, with limited evidence of transformational adaptation and negligible evidence of risk reduction outcomes. We identify eight priorities for global adaptation research: assess the effectiveness of adaptation responses, enhance the understanding of limits to adaptation, enable individuals and civil society to adapt, include missing places, scholars and scholarship, understand private sector responses, improve methods for synthesizing different forms of evidence, assess the adaptation at different temperature thresholds, and improve the inclusion of timescale and the dynamics of responses
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