Fant 10203 publikasjoner. Viser side 391 av 409:
Two-Stage Feature Engineering to Predict Air Pollutants in Urban Areas
Air pollution is a global challenge to human health and the ecological environment. Identifying the relationship among pollutants, their fundamental sources and detrimental effects on health and mental well-being is critical in order to implement appropriate countermeasures. The way forward to address this issue and assess air quality is through accurate air pollution prediction. Such prediction can subsequently assist governing bodies in making prompt, evidence-based decisions and prevent further harm to our urban environment, public health, and climate, all of which co-benefit our economy. In this study, the main objective is to explore the strength of features and proposed a two stage feature engineering approach, which fuses the advantage of influential factors along with the decomposition approach and generates an optimum feature combination for five major pollutants including Nitrogen Dioxide (NO 2 ), Ozone (O 3 ), Sulphur Dioxide (SO 2 ), and Particulate Matter (PM2.5, and PM10). The experiments are conducted using a dataset from 2015 to 2020 which is publicly available and is collected from Belfast-based air quality monitoring stations in Northern Ireland, UK. In stage-1, using the dataset new features such as trigonometric and statistical features are created to capture their dependency on the target pollutant and generated correlation-inspired best feature combinations to improve forecasting model performance. This is further enhanced in stage-2 by an optimum feature combination which is an integration of stage-1 and Variational Mode Decomposition (VMD) based features. This study employed a simplified Long Short Term Memory (LSTM) neural network and proposed a single-step forecasting model to predict multivariate time series data. Three performance indicators are used to evaluate the effectiveness of forecasting model: (a) root mean square error (RMSE), (b) mean absolute error (MAE), and (c) R-squared (R 2 ). The results demonstrate the effectiveness of proposed approach with 13% improvement in performance (in terms of R 2 ) and the lowest error scores for both RMSE and MAE.
2024
2024
Anthropogenic activities emit ~2,000 Mg y−1 of the toxic pollutant mercury (Hg) into the atmosphere, leading to long-range transport and deposition to remote ecosystems. Global anthropogenic emission inventories report increases in Northern Hemispheric (NH) Hg emissions during the last three decades, in contradiction with the observed decline in atmospheric Hg concentrations at NH measurement stations. Many factors can obscure the link between anthropogenic emissions and atmospheric Hg concentrations, including trends in the reemissions of previously released anthropogenic (“legacy”) Hg, atmospheric sink variability, and spatial heterogeneity of monitoring data. Here, we assess the observed trends in gaseous elemental mercury (Hg0) in the NH and apply biogeochemical box modeling and chemical transport modeling to understand the trend drivers. Using linear mixed effects modeling of observational data from 51 stations, we find negative Hg0 trends in most NH regions, with an overall trend for 2005 to 2020 of −0.011 ± 0.006 ng m−3 y−1 (±2 SD). In contrast to existing emission inventories, our modeling analysis suggests that annual NH anthropogenic emissions must have declined by at least 140 Mg between the years 2005 and 2020 to be consistent with observed trends. Faster declines in 95th percentile Hg0 values than median values in Europe, North America, and East Asian measurement stations corroborate that the likely cause is a decline in nearby anthropogenic emissions rather than background legacy reemissions. Our results are relevant for evaluating the effectiveness of the Minamata Convention on Mercury, demonstrating that existing emission inventories are incompatible with the observed Hg0 declines.
2024
2024
Måling av gasser i Statsarkivets lokaler i Trondheim. Fase 2 - 2024
Denne rapporten viser resultater fra fase 2 i måleprosjektet NILU har utført ved Statsarkivet i Trondheim. Det er gjort prøvetaking og analyse i en periode på sju dager fra 23. til 30. mai ved to lokaliteter, én innendørs og én utendørs. Totalkonsentrasjonen av VOC’er (TVOC) ble målt til 135 µg/m3 gitt som toluen-ekvivalenter ved lokaliteten inne (MAG A, Reol 097) og 33 µg/m3 ved lokaliteten ute. Resultatene synliggjør effekten av innendørs ventilasjonssystemer og begge studiene vil brukes av Statsarkivet i sitt videre arbeid med innendørs luftkvalitet.
NILU
2024
2024
2024
2024
This study examines how southern wintering areas may contribute to organochlorine (OCs) loads in arctic seabirds during breeding. Light-sensitive geolocators (GLS loggers) were deployed on Arctic skuas (Stercorarius parasiticus) in one high arctic and two subarctic colonies. Hexcahlorobenzene (HCB), chlordanes, mirex, p,p′-dichlorodiphenyldichloro-ethylene (p,p′-DDE), and polychlorinated biphenyls (PCBs) were measured in the blood of breeding adults at the nest (58 individuals, a total of 128 samples) in northern Norway and Svalbard between 2009 and 2015. We compared OC concentrations and OC profiles among nesting skuas wintering in five Atlantic regions, determined by the GLS loggers: the coast of Argentina, the Caribbean, off West Africa, off the coast of southern Africa, and the Mediterranean Sea. As predicted, HCB, which is semi-volatile and has high long-range transport potential, showed high prevalence in birds wintering in all regions except the Mediterranean. Mirex showed the highest prevalence in birds wintering off the coasts of Argentina and southern Africa, in accordance with high background levels previously documented in the Southern Ocean. Chlordanes were particularly prevalent in skuas wintering off southern Africa, whereas p,p′-DDE seemed relatively evenly distributed among wintering areas. As predicted, the prevalence of PCBs was much higher in birds wintering in the Mediterranean Sea than in birds from other regions. This study thus suggests that the Mediterranean Sea and the mid- and southern Atlantic are essential sources of different OCs in the blood of Arctic skuas breeding in the European Arctic.
2025
This study critically examines the workflow for untargeted analysis of volatile organic compounds (VOCs) in ambient air, from sampling strategies to data interpretation by using GC-HRMS. While untargeted approaches are well-established in liquid chromatography (LC) due to advanced-deconvolution tools and extensive metabolomic libraries, their application in gas chromatography (GC) remains less developed, particularly for VOCs. The high structural isomerism of VOCs and the relative novelty of GC-based untargeted methodologies present unique challenges, including limited software tools and reference libraries. Air samples from suburban and rural sites in central Italy were analyzed to explore chemical diversity and address methodological gaps. This study evaluates critical decisions, such as sampling strategies, extraction techniques, and data-processing workflows, highlighting the limitations of automated deconvolution tools and the need for manual validation. Results revealed distinct source contributions, with suburban areas showing higher levels of anthropogenic compounds and rural areas dominated by biogenic emissions. This work underscores the potential of GC-HRMS untargeted analysis to advance environmental chemistry, while addressing key pitfalls and providing practical recommendations for reliable application. By bridging methodological gaps, it offers a roadmap for future studies aiming to integrate untargeted and targeted approaches in air quality research.
2025
This document provides technical details and support for the implementation of air quality monitoring under the Directive (EU) 2024/2881 of the European Parliament and of the Council of 23 October 2024 on ambient air quality and cleaner air for Europe (recast) (AAQD, Directive (EU) 2024/2881). It presents an overview of current knowledge and best practices, signposting to existing technical guidance on air quality monitoring and to sources of ongoing technical guidance development. This document does not formulate any legal provisions and as such, it does not have a legally binding value.
Publications Office of the European Union/European Commission. Directorate-General for Environment
2025
This report presents data from the fourth year of a five-year period of the MILFERSK program. In 2024, the monitoring program focused on the sampling and analysis of the benthic food chain in Lake Mjøsa, encompassing the following sample types: Chironomids, Ruffe, Perch, Pike and the stomach contents of ruffe. Additionally, brown trout from the pelagic zone in Lake Mjøsa were collected and analyzed, with the contaminant levels compared to samples of brown trout from the reference lake, Femunden. The concentrations of 175 individual compounds/isomers were determined, with frequent detections of specific per- and polyfluoroalkyl substances (PFAS), polybrominated diphenyl ethers (PBDEs), mercury (Hg), and siloxanes exhibiting biomagnifying properties throughout the food chain. Certain contaminants, such as quaternary ammonium compounds, were found in higher concentrations in sediment and lower trophic levels. Concentrations of chlorinated paraffins (CPs), particularly medium-chain chlorinated paraffins (MCCPs) were higher in chironomids, ruffe, and the livers of perch and pike, compared to levels observed in 2021 and 2022, with an increase up the food chain in 2024. A slight downward trend in perfluorooctane sulfonate (PFOS) concentrations was observed in Lake Mjøsa from 2014 – 2024. Additionally, a lower length-adjusted mercury concentration was noted for brown trout in Lake Mjøsa during the period from 2015 to 2024, compared to the preceding nine years (2006 – 2014).
Norsk institutt for vannforskning (NIVA)
2025
2025
2025
Abstract. Establishing interlaboratory compatibility among measurements of stable isotope ratios of atmospheric methane (δ13C-CH4 and δD-CH4) is challenging. Significant offsets are common because laboratories have different ties to the VPDB or SMOW-SLAP scales. Umezawa et al. (2018) surveyed numerous comparison efforts for CH4 isotope measurements conducted from 2003 to 2017 and found scale offsets of up to 0.5 ‰ for δ13C-CH4 and 13 ‰ for δD-CH4 between laboratories. This exceeds the World Meteorological Organisation Global Atmospheric Watch (WMO-GAW) network compatibility targets of 0.02 ‰ and 1 ‰ considerably. We employ a method to establish scale offsets between laboratories using their reported CH4 isotope measurements on atmospheric samples. Our study includes data from eight laboratories with experience in high-precision isotope ratio mass spectrometry (IRMS) measurements for atmospheric CH4. The analysis relies exclusively on routine atmospheric measurements conducted by these laboratories at high-latitude stations in the Northern and Southern Hemispheres, where we assume each measurement represents sufficiently well-mixed air at the latitude for direct comparison. We use two methodologies for interlaboratory comparisons: (I) assessing differences between time-adjacent observation data and (II) smoothing the observed data using polynomial and harmonic functions before comparison. The results of both methods are consistent, and with a few exceptions, the overall average offsets between laboratories align well with those reported by Umezawa et al. (2018). This indicates that interlaboratory offsets remain robust over multi-year periods. The evaluation of routine measurements allows us to calculate the interlaboratory offsets from hundreds, in some cases thousands of measurements. Therefore, the uncertainty in the mean interlaboratory offset is not limited by the analytical error of a single analysis but by real atmospheric variability between the sampling dates and stations. Using the same method, we assess this uncertainty by investigating measurements from four high-latitude sites analysed by the INSTAAR laboratory. After applying the derived interlaboratory offsets, we present a harmonised time series for δ13C-CH4 and δD-CH4 at high northern and southern latitudes, covering the period from 1988 to 2023.
2025
2025
Spatial and temporal assessment of soil degradation risk in Europe
Soil degradation threatens agricultural productivity and ecosystem resilience across Europe, yet spatially consistent assessments of its intensity and drivers remain limited. In this study, we used Soil Degradation Proxy (SDP), that integrates four key indicators of soil degradation, including erosion rate, soil pH, electrical conductivity, and organic carbon content, to quantify soil degradation risk. Using over 38,000 LUCAS topsoil observations and a machine learning model trained on climate, land cover, topographic, soil parent material properties, and spectral variables, we map annual SDP values between years 2000 to 2022 across Europe. Results show soil degradation risk is highest in southern Europe, especially in intensively managed and sparsely vegetated landscapes. Over the past two decades, approximately 7.1% of land area across the EU and the UK has experienced increasing degradation risk (most notably across Eastern Europe), with rainfed croplands emerging as the most affected land cover type. Land cover is the most influential driver, modulating effects of climatic variables such as precipitation and temperature on SDP. This data-driven framework provides a consistent and scalable approach for monitoring soil degradation risk and offers actionable insights to support targeted conservation and EU-wide policy implementation.
2025