Found 9887 publications. Showing page 326 of 396:
Ren luft for alle. ExtraStiftelsen project 2019/HE1-263918.
In 2019, in the framework of Oslo being European Green Capital, NILU invited students from elementary schools to
measure air pollution in their neighbourhood, using simple and affordable measuring methods based on paper and
Vaseline. The students prepared the measuring devices and selected the places where they wanted to monitor. After one
week, they retrieved the devices and used a scale to compare the amount of dust fastened to the Vaseline. All of the data
gathered by the students was uploaded by the teachers to a website (https://luftaforalle.nilu.no/), where a map showed all the results from the participating schools. The school campaign has helped researchers to get data on particulate matter from many places where data was not available, and has increased awareness among the children about the sustainability challenges cities are facing.
NILU
2021
Quality assurance and quality control procedure for national and Union GHG projections 2021
The quality assurance and quality control (QA/QC) procedure is an element of the QA/QC programme of the Union system for policies and measures and projections to be established in 2021 according to Article 39 of the Regulation on the Governance of the Energy Union and Climate Action (EU) 2018/1999. The European Environment Agency (EEA) is responsible for the annual implementation of the QA/QC procedures and is assisted by the European Topic Centre on Climate Change Mitigation and Energy (ETC/CME). The QA/QC procedure document describes QA/QC checks carried out at EU level on the national reported projections from Member States and on the compiled Union GHG projections. QA/QC procedures are performed at several different stages during the preparation of the national and Union GHG projections in order to aim to ensure the timeliness, transparency, accuracy, consistency, comparability and completeness of the reported information. The results of the 2021 QA/QC procedure are presented in the related paper ETC/CME Eionet Report 8/2021.
ETC/CME
2021
Why is the city's responsibility for its air pollution often underestimated? A focus on PM2.5
While the burden caused by air pollution in urban areas is well documented, the origin of this pollution and therefore the responsibility of the urban areas in generating this pollution are still a subject of scientific discussion. Source apportionment represents a useful technique to quantify the city's responsibility, but the approaches and applications are not harmonized and therefore not comparable, resulting in confusing and sometimes contradicting interpretations. In this work, we analyse how different source apportionment approaches apply to the urban scale and how their building elements and parameters are defined and set. We discuss in particular the options available in terms of indicator, receptor, source, and methodology. We show that different choices for these options lead to very large differences in terms of outcome. For the 150 large EU cities selected in our study, different choices made for the indicator, the receptor, and the source each lead to an average difference of a factor of 2 in terms of city contribution. We also show that temporal- and spatial-averaging processes applied to the air quality indicator, especially when diverging source apportionments are aggregated into a single number, lead to the favouring of strategies that target background sources while occulting actions that would be efficient in the city centre. We stress that methodological choices and assumptions most often lead to a systematic and important underestimation of the city's responsibility, with important implications. Indeed, if cities are seen as a minor actor, plans will target the background as a priority at the expense of potentially effective local actions.
2021
Brominated Flame Retardants in Antarctic Air in the Vicinity of Two All-Year Research Stations
Continuous atmospheric sampling was conducted between 2010–2015 at Casey station in Wilkes Land, Antarctica, and throughout 2013 at Troll Station in Dronning Maud Land, Antarctica. Sample extracts were analyzed for polybrominated diphenyl ethers (PBDEs), and the naturally converted brominated compound, 2,4,6-Tribromoanisole, to explore regional profiles. This represents the first report of seasonal resolution of PBDEs in the Antarctic atmosphere, and we describe conspicuous differences in the ambient atmospheric concentrations of brominated compounds observed between the two stations. Notably, levels of BDE-47 detected at Troll station were higher than those previously detected in the Antarctic or Southern Ocean region, with a maximum concentration of 7800 fg/m3. Elevated levels of penta-formulation PBDE congeners at Troll coincided with local building activities and subsided in the months following completion of activities. The latter provides important information for managers of National Antarctic Programs for preventing the release of persistent, bioaccumulative, and toxic substances in Antarctica.
MDPI
2021
Information Requirements under the Essential-Use Concept: PFAS Case Studies
Per- and polyfluoroalkyl substances (PFAS) are a class of substances for which there are widespread concerns about their extreme persistence in combination with toxic effects. It has been argued that PFAS should only be employed in those uses that are necessary for health or safety or are critical for the functioning of society and where no alternatives are available (“essential-use concept”). Implementing the essential-use concept requires a sufficient understanding of the current uses of PFAS and of the availability, suitability, and hazardous properties of alternatives. To illustrate the information requirements under the essential-use concept, we investigate seven different PFAS uses, three in consumer products and four industrial applications. We investigate how much information is available on the types and functions of PFAS in these uses, how much information is available on alternatives, their performance and hazardous properties and, finally, whether this information is sufficient as a basis for deciding on the essentiality of a PFAS use. The results show (i) the uses of PFAS are highly diverse and information on alternatives is often limited or lacking; (ii) PFAS in consumer products often are relatively easy to replace; (iii) PFAS uses in industrial processes can be highly complex and a thorough evaluation of the technical function of each PFAS and of the suitability of alternatives is needed; (iv) more coordination among PFAS manufacturers, manufacturers of alternatives to PFAS, users of these materials, government authorities, and other stakeholders is needed to make the process of phasing out PFAS more transparent and coherent.
2021
2021
2021
Transboundary particulate matter, photo-oxidants, acidifying and eutrophying components
Norwegian Meteorological Institute
2021
Observed and Modeled Black Carbon Deposition and Sources in the Western Russian Arctic 1800−2014
Black carbon (BC) particles contribute to climate warming by heating the atmosphere and reducing the albedo of snow/ice surfaces. The available Arctic BC deposition records are restricted to the Atlantic and North American sectors, for which previous studies suggest considerable spatial differences in trends. Here, we present first long-term BC deposition and radiocarbon-based source apportionment data from Russia using four lake sediment records from western Arctic Russia, a region influenced by BC emissions from oil and gas production. The records consistently indicate increasing BC fluxes between 1800 and 2014. The radiocarbon analyses suggest mainly (∼70%) biomass sources for BC with fossil fuel contributions peaking around 1960–1990. Backward calculations with the atmospheric transport model FLEXPART show emission source areas and indicate that modeled BC deposition between 1900 and 1999 is largely driven by emission trends. Comparison of observed and modeled data suggests the need to update anthropogenic BC emission inventories for Russia, as these seem to underestimate Russian BC emissions and since 1980s potentially inaccurately portray their trend. Additionally, the observations may indicate underestimation of wildfire emissions in inventories. Reliable information on BC deposition trends and sources is essential for design of efficient and effective policies to limit climate warming.
2021
Pollutants emitted by industrial processes are deposited across the landscape. Ice core records from mid-latitude glaciers located close to emission sources document the history of local-to-regional pollution since preindustrial times. Such records underpin attribution of pollutants to specific emission sources critical to developing abatement policies. Previous ice core studies from the Alps document the overall magnitude and timing of pollution related to nitrogen and sulfur-derived species, as well as a few metals including lead. Here, we used subannually resolved measurements of vanadium (V) and molybdenum (Mo) in two ice cores from Col du Dome (French Alps), as well as atmospheric transport and deposition modeling, to investigate sources of pollution in the free European troposphere. The noncrustal V and Mo (ncV, ncMo) components were calculated by subtracting the crustal component from the total concentration. These ice core results showed a 32-fold increase in ncV and a 69-fold increase in ncMo from the preindustrial era (pre-1860) to the industrial concentration peaks. Anthropogenic V and Mo emissions in Europe were estimated using emission factors from oil and coal consumption and atmospheric transport and deposition modeling. When comparing ice core data to estimated anthropogenic V and Mo emissions in Europe, V was found to be sourced primarily from oil combustion emissions. Conversely, coal and oil combustion estimated emissions did not agree with the measured ice core Mo concentrations, suggesting that other anthropogenic Mo sources dominated coal-burning emissions, particularly after the 1950s. Noncoal-burning sources of Mo may include metallurgy although emission factors are poorly known.
American Geophysical Union (AGU)
2021
The effect of the 2018 extreme meteorological conditions in Europe on methane (CH4) emissions is examined using estimates from four atmospheric inversions calculated for the period 2005–2018. For most of Europe, we find no anomaly in 2018 compared to the 2005–2018 mean. However, we find a positive anomaly for the Netherlands in April, which coincided with positive temperature and soil moisture anomalies suggesting an increase in biogenic sources. We also find a negative anomaly for the Netherlands for September–October, which coincided with a negative anomaly in soil moisture, suggesting a decrease in soil sources. In addition, we find a positive anomaly for Serbia in spring, summer and autumn, which coincided with increases in temperature and soil moisture, again suggestive of changes in biogenic sources, and the annual emission for 2018 was 33 ± 38% higher than the 2005–2017 mean. These results indicate that CH4 emissions from areas where the natural source is thought to be relatively small can still vary due to meteorological conditions. At the European scale though, the degree of variability over 2005–2018 was small, and there was negligible impact on the annual CH4 emissions in 2018 despite the extreme meteorological conditions.
This article is part of a discussion meeting issue ‘Rising methane: is warming feeding warming? (part 2)’.
2021
2021
2021
Editorial for the Special Issue From Nanoinformatics to Nanomaterials Risk Assessment and Governance
MDPI
2021
Målinger av PM10 i Lohavn. April og mai 2020.
NILU – Norsk institutt for luftforskning har på oppdrag fra HAV Eiendom utført målinger av svevestøv (PM10) i Lohavn i Oslo. Området skal utvikles til et nytt byområde med boliger, skole, utearealer og næring. PM-konsentrasjonen ble målt på tre steder i Lohavn for å kartlegge svevestøvkonsentrasjonen og mulige kilder. Måleprosjektet pågikk våren 2020. Mulige effekter av Covid-nedstengning, variasjoner i trafikkmengden i området og variasjoner av meteorologiske parametere på PM-konsentrasjonen er diskutert.
Måleresultatene viser lavere PM-konsentrasjon enn i måleperioden 2016/17. Årsaken var trolig bortfall av midlertidige kilder som førte til periodevis høye konsentrasjoner i 2016/17. De høyeste PM10-konsentrasjonene ble observert ved vind fra sør-sørvest (som dominerer på dagtid).
NILU
2021
Målinger av SO2 i omgivelsene til Elkem Carbon og REC Solar. Januar 2020 – desember 2020.
På oppdrag fra Elkem Carbon AS har NILU utført målinger av SO2 i omgivelsene til Elkem Carbon og REC Solar i Vågsbygd
(Kristiansand kommune). Bedriftene ble pålagt av Miljødirektoratet å gjennomføre SO2-målinger i omgivelsesluft.
Målingene ble utført med SO2-monitor i boligområdet på Fiskåtangen (Konsul Wilds vei) og med passive SO2-prøvetakere
ved 6 steder rundt bedriftene. Rapporten dekker målinger i perioden 1. januar 2020 – 31. desember 2020.
Norske grenseverdier for luftkvalitet (SO2) ble overholdt ved Konsul Wilds vei for alle midlingsperioder krevet i
forurensningsforskriften (årsmiddel, vintermiddel, døgnmiddel og timemiddel). De mest belastede stedene i måleperioden
var Konsul Wilds vei og Fiskåveien rett sør for bedriftene.
NILU
2021
Modeling study of the impact of SO2 volcanic passive emissions on the tropospheric sulfur budget
Well constrained volcanic emissions inventories in chemistry transport models are necessary to study the impacts induced by these sources on the tropospheric sulfur composition and on sulfur species concentrations and depositions at the surface. In this paper, the changes induced by the update of the volcanic sulfur emissions inventory are studied using the global chemistry transport model MOCAGE (MOdèle de Chimie Atmosphérique à Grande Échelle). Unlike the previous inventory (Andres and Kasgnoc, 1998), the updated one (Carn et al., 2016, 2017) uses more accurate information and includes contributions from both passive degassing and eruptive emissions. Eruptions are provided as daily total amounts of sulfur dioxide (SO2) emitted by volcanoes in the Carn et al. (2016, 2017) inventories, and degassing emissions are provided as annual averages with the related mean annual uncertainties of those emissions by volcano. Information on plume altitudes is also available and has been used in the model. We chose to analyze the year 2013, for which only a negligible amount of eruptive volcanic SO2 emissions is reported, allowing us to focus the study on the impact of passive degassing emissions on the tropospheric sulfur budget. An evaluation against the Ozone Monitoring Instrument (OMI) SO2 total column and MODIS (Moderate-Resolution Imaging Spectroradiometer) aerosol optical depth (AOD) observations shows the improvements of the model results with the updated inventory. Because the global volcanic SO2 flux changes from 13 Tg yr−1 in Andres and Kasgnoc (1998) to 23.6 Tg yr−1 in Carn et al. (2016, 2017), significant differences appear in the global sulfur budget, mainly in the free troposphere and in the tropics. Even though volcanic SO2 emissions represent 15 % of the total annual sulfur emissions, the volcanic contribution to the tropospheric sulfate aerosol burden is 25 %, which is due to the higher altitude of emissions from volcanoes. Moreover, a sensitivity study on passive degassing emissions, using the annual uncertainties of emissions per volcano, also confirmed the nonlinear link between tropospheric sulfur species content with respect to volcanic SO2 emissions. This study highlights the need for accurate estimates of volcanic sources in chemistry transport models in order to properly simulate tropospheric sulfur species.
2021
Long-term monitoring of regulated organic chemicals, such as legacy persistent organic pollutants (POPs) and polycyclic aromatic hydrocarbons (PAHs), in ambient air provides valuable information about the compounds' environmental fate as well as temporal and spatial trends. This is the foundation to evaluate the effectiveness of national and international regulations for priority pollutants. Extracts of high-volume air samples, collected on glass fibre filters (GFF for particle phase) and polyurethane foam plugs (PUF for gaseous phase), for targeted analyses of legacy POPs are commonly cleaned by treatment with concentrated sulfuric acid, resulting in extracts clean from most interfering compounds and matrices that are suitable for multi-quantitative trace analysis. Such standardised methods, however, severely restrict the number of analytes for quantification and are not applicable when targeting new and emerging compounds as some may be less stable under acid treatment. Recently developed suspect and non-target screening analytical strategies (SUS and NTS, respectively) are shown to be effective evaluation tools aimed at identifying a high number of compounds of emerging concern. These strategies, combining highly sophisticated analytical technology with extensive data interpretation and statistics, are already widely accepted in environmental sciences for investigations of various environmental matrices, but their application to air samples is still very limited. In order to apply SUS and NTS for the identification of organic contaminants in air samples, an adapted and more wide-scope sample clean-up method is needed compared to the traditional method, which uses concentrated sulfuric acid. Analysis of raw air sample extracts without clean-up would generate extensive contamination of the analytical system, especially with PUF matrix-based compounds, and thus highly interfered mass spectra and detection limits which are unacceptable high for trace analysis in air samples.
In this study, a novel wide-scope sample clean-up method for high-volume air samples has been developed and applied to real high-volume air samples, which facilitates simultaneous target, suspect and non-target analyses. The scope and efficiency of the method were quantitatively evaluated with organic compounds covering a wide range of polarities (logP 2–11), including legacy POPs, brominated flame retardants (BFRs), chlorinated pesticides and currently used pesticides (CUPs). In addition, data reduction and selection strategies for SUS and NTS were developed for comprehensive two-dimensional gas chromatography separation with low-resolution time-of-flight mass spectrometric detection (GC × GC-LRMS) data and applied to real high-volume air samples. Combination of the newly developed clean-up procedure and data treatment strategy enabled the prioritisation of over 600 compounds of interest in the particle phase (on GFF) and over 850 compounds in the gas phase (on PUF) out of over 25 000 chemical features detected in the raw dataset. Of these, 50 individual compounds were identified and confirmed with reference standards, 80 compounds were identified with a probable structure, and 774 compounds were assigned to various compound classes. In the dataset available here, 11 hitherto unknown halogenated compounds were detected. These unknown compounds were not yet listed in the available mass spectral libraries.
2021
A strategy towards the generation of testable adverse outcome pathways for nanomaterials
Manufactured nanomaterials (NMs) are increasingly used in a wide range of industrial applications leading to a constant increase in the market size of nano-enabled products. The increased production and use of NMs are constantly raising concerns among different stakeholder groups with regard to their effects on human and environmental health. Currently, nanosafety hazard assessment is still widely performed using in vivo (animal) models, however the development of robust and regulatory relevant strategies is required to prioritize and/or reduce animal testing. Adverse outcome pathways (AOPs) are a structured representation of biological events that start from a molecular initiating event (MIE) leading to an adverse outcome (AO) through a series of key events (KEs). The AOP framework offers great advancement to risk assessment and regulatory safety assessments. While AOPs for chemicals have been more frequently reported, AOPs collection for NMs is narrow. By using existing AOPs, we aimed to generate simple and testable strategies to predict if a given NM has the potential to induce a MIE leading to an AO through a series of KEs. Firstly, we identified potential MIEs or initial KEs reported for NMs in the literature. Then, we searched the identified MIE or initial KEs as keywords in the AOP-Wiki to find associated AOPs. Finally, using two case studies, we demonstrated here how in vitro strategies can be used for testing the identified MIE/KEs.
Springer
2021