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South Africa is the largest national source of industrial atmospheric pollutants in Africa, and the emission of acid-forming pollutants occurs mainly in the eastern Highveld region of the country. However, spatial information on deposition is very sparse beyond the primary emissions zone. Here we quantify wet and dry deposition at four sites from the far northern savanna (Vaalwater) through the grasslands of the interior coal-producing belt of Mpumalanga (Elandsfontein) and the remote KwaZulu Natal Drakensberg mountains (Cathedral Peak) to the fynbos of the southern coast of the country (Knysna), a distance of over 1200 km. Rainwater samples were collected using automated wet-only samplers and analysed for mineral ions and water-soluble organic acids. Wet deposition fluxes were driven largely by rainfall amount rather than differences in chemical composition for three inland sites, with the highest wet deposited sulphur (S) (5.1 kgS/ha/year) and nitrogen (N) (6.9 kgN/ha/year) found in the Drakensberg mountains, greatly expanding the potentially harmful deposition footprint beyond the industrialised Highveld zone. Furthermore, the study period covered the extreme drought years of 2015–2016; hence, wet deposition fluxes could be significantly underestimated relative to more average rainfall years. Dry deposition fluxes, estimated using passive samplers and inferential methods, were far higher at the industrial Highveld site. Overall, total (wet + dry) deposition of S was greatest at the Highveld site (12.0 kgS/ha/year), but the greatest total N deposition (7.0 kgN/ha/year) was found at the remote Drakensberg site. Measured levels of both S and N deposition are well within the ranges found to cause acidification of soils and surface waters in northern hemisphere studies, or changes in vegetation species composition, and could be much higher in more typical, wetter years.
2022
2005
2015
2004
2005
2023
Rapid identification of in vitro cell toxicity using an electrochemical membrane screening platform
This study compares the performance and output of an electrochemical phospholipid membrane platform against respective in vitro cell-based toxicity testing methods using three toxicants of different biological action (chlorpromazine (CPZ), colchicine (COL) and methyl methanesulphonate (MMS)). Human cell lines from seven different tissues (lung, liver, kidney, placenta, intestine, immune system) were used to validate this physicochemical testing system. For the cell-based systems, the effective concentration at 50 % cell death (EC50) values are calculated. For the membrane sensor, a limit of detection (LoD) value was extracted as a quantitative parameter describing the minimum concentration of toxicant which significantly affects the structure of the phospholipid sensor membrane layer. LoD values were found to align well with the EC50 values when acute cell viability was used as an end-point and showed a similar toxicity ranking of the tested toxicants. Using the colony forming efficiency (CFE) or DNA damage as end-point, a different order of toxicity ranking was observed. The results of this study showed that the electrochemical membrane sensor generates a parameter relating to biomembrane damage, which is the predominant factor in decreasing cell viability when in vitro models are acutely exposed to toxicants. These results lead the way to using electrochemical membrane-based sensors for rapid relevant preliminary toxicity screens.
2023
2012
Norge skal etter 2001 årlig rapportere til EU luftforurensningstilstanden i alle soner i landet. Rapporten presenterer et forslag til databasert verktøy som vil effektivisere denne rapporteringen. Verktøyet er GIS-basert, og konseptet er å visualisere tilstanden i sonene ved hjelp av tallverdier og isolinjer på kart, med zooming -mulighet.
1999
1999
2002
The aim of this project was to collect, integrate and analyse observations of climate-relevant aerosol parameters (aerosol optical depth (AOD), Ångstrøm exponent (AE), black carbon (BC)) in and around Svalbard. These observations have been performed at different places and with different instrument types, the analysis procedures of which follow different protocols. Annual merged datasets of AOD, AE and BC have been provided to the SIOS Data Management System and are now available for network-wide use in, e.g., Arctic climate and pollution studies. The analysis of the 2002-2020 data have confirmed earlier results showing a good correlation between measurements in Ny-Ålesund and Hornsund, but not a high degree of short-term agreement due to aerosol variability arising from geographical locations and local conditions. There is also a clear link between the columnar AOD/AE-measurements and in-situ aerosol measurements at Gruvebadet Observatory, while a comparison of in-situ measurements at Gruvebadet and Zeppelin Observatory shows deviations varying with season.
NILU
2022
2006
2006
2010
Low concentrations of 106Ru were detected across Europe at the turn of September and October 2017. The origin of 106Ru has still not been confirmed; however, current studies agree that the release occurred probably near Mayak in the southern Urals. The source reconstructions are mostly based on an analysis of concentration measurements coupled with an atmospheric transport model. Since reasonable temporal resolution of concentration measurements is crucial for proper source term reconstruction, the standard 1-week sampling interval could be limiting. In this paper, we present an investigation of the usability of the newly developed AMARA (Autonomous Monitor of Atmospheric Radioactive Aerosol) and CEGAM (carousel gamma spectrometry) real-time monitoring systems, which are based on the gamma-ray counting of aerosol filters and allow for determining the moment when 106Ru arrived at the monitoring site within approx. 1 h and detecting activity concentrations as low as several mBq m−3 in 4 h intervals. These high-resolution data were used for inverse modeling of the 106Ru release. We perform backward runs of the Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) atmospheric transport model driven with meteorological data from the Global Forecast System (GFS), and we construct a source–receptor sensitivity (SRS) matrix for each grid cell of our domain. Then, we use our least squares with adaptive prior covariance (LS-APC) method to estimate possible locations of the release and the source term of the release. With Czech monitoring data, the use of concentration measurements from the standard regime and from the real-time regime is compared, and a better source reconstruction for the real-time data is demonstrated in the sense of the location of the source and also the temporal resolution of the source. The estimated release location, Mayak, and the total estimated source term, 237±107 TBq, are in agreement with previous studies. Finally, the results based on the Czech monitoring data are validated with the IAEA-reported (International Atomic Energy Agency) dataset with a much better spatial resolution, and the agreement between the IAEA dataset and our reconstruction is demonstrated. In addition, we validated our findings also using the FLEXPART (FLEXible PARTicle dispersion) model coupled with meteorological analyses from the European Centre for Medium-Range Weather Forecasts (ECMWF).
2021
This study introduces an Earth observation (EO)-based system which is capable of operationally estimating and continuously monitoring the ultraviolet index (UVI) in Europe. UVIOS (i.e., UV-Index Operating System) exploits a synergy of radiative transfer models with high-performance computing and EO data from satellites (Meteosat Second Generation and Meteorological Operational Satellite-B) and retrieval processes (Tropospheric Emission Monitoring Internet Service, Copernicus Atmosphere Monitoring Service and the Global Land Service). It provides a near-real-time nowcasting and short-term forecasting service for UV radiation over Europe. The main atmospheric inputs for the UVI simulations include ozone, clouds and aerosols, while the impacts of ground elevation and surface albedo are also taken into account. The UVIOS output is the UVI at high spatial and temporal resolution (5 km and 15 min, respectively) for Europe (i.e., 1.5 million pixels) in real time. The UVI is empirically related to biologically important UV dose rates, and the reliability of this EO-based solution was verified against ground-based measurements from 17 stations across Europe. Stations are equipped with spectral, broadband or multi-filter instruments and cover a range of topographic and atmospheric conditions. A period of over 1 year of forecasted 15 min retrievals under all-sky conditions was compared with the ground-based measurements. UVIOS forecasts were within ±0.5 of the measured UVI for at least 70 % of the data compared at all stations. For clear-sky conditions the agreement was better than 0.5 UVI for 80 % of the data. A sensitivity analysis of EO inputs and UVIOS outputs was performed in order to quantify the level of uncertainty in the derived products and to identify the covariance between the accuracy of the output and the spatial and temporal resolution and the quality of the inputs. Overall, UVIOS slightly overestimated the UVI due to observational uncertainties in inputs of cloud and aerosol. This service will hopefully contribute to EO capabilities and will assist the provision of operational early warning systems that will help raise awareness among European Union citizens of the health implications of high UVI doses.
2021
Real-world application of new sensor technologies for air quality monitoring. ETC/ACM Technical Paper, 2013/16
2013
2015
REanalysis of the TROpospheric chemical composition over the past 40 years. A long-term global modeling study of tropospheric chemistry funded under the 5th EU framework programme. Reports on Earth System Science, 48/2007
2007