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Found 10000 publications. Showing page 329 of 400:

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Spatial trends of chlorinated paraffins and dechloranes in air and soil in a tropical urban, suburban, and rural environment

Nipen, Maja; Vogt, Rolf David; Bohlin-Nizzetto, Pernilla; Borgå, Katrine; Mwakalapa, Eliezer Brown; Borgen, Anders; Jørgensen, Susanne Jøntvedt; Ntapanta, Samwel Moses; Mmochi, Aviti John; Schlabach, Martin; Breivik, Knut

There are large knowledge gaps concerning environmental levels and fate of many organic pollutants, particularly for chemicals of emerging concern in tropical regions of the Global South. In this study, we investigated the levels of chlorinated paraffins (CPs) and dechloranes in air and soil in rural, suburban, and urban regions in and around Dar es Salaam, Tanzania. Samples were also collected near the city's main municipal waste dumpsite and an electronic waste (e-waste) handling facility. In passive air samples, short chain CPs (SCCPs) dominated, with an average estimated concentration of 22 ng/m3, while medium chain CPs (MCCPs) had an average estimated concentration of 9 ng/m3. The average estimated air concentration of ∑dechloranes (Dechlorane Plus (DP) + Dechlorane 602 + Dechlorane 603) was three to four orders of magnitudes lower, 2 pg/m3. In soil samples, MCCPs dominated with an average concentration of 640 ng/g dw, followed by SCCPs with an average concentration of 330 ng/g dw, and ∑dechloranes with an average concentration of 0.9 ng/g dw. In both air and soil, DP was the dominating dechlorane compound. Urban pulses were observed for CPs and dechloranes in air and soil. CPs were in addition found in elevated levels at the municipal waste dumpsite and the e-waste handling facility, while DPs were found in elevated levels at the e-waste handling facility. This suggests that waste handling sites represent important emission sources for these pollutants. Investigations into seasonal trends and environmental fate of CPs and dechloranes showed that monsoonal rain patterns play a major role in governing air concentrations and mobility, particularly for the less volatile MCCPs and dechloranes. This study is the first to report levels of CPs in air from sub-Saharan Africa, and DP, Dechlorane 602, and Dechlorane 603 in soil from sub-Saharan Africa.

2021

Effects of extreme meteorological conditions in 2018 on European methane emissions estimated using atmospheric inversions

Thompson, Rona Louise; Zwaaftink, Christine Groot; Brunner, D; Tsuruta, Aki; Aalto, T; Raivonen, M; Crippa, M.; Solazzo, Efisio; Guizzardi, D.; Regnier, P.; Maisonnier, M.

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

Impact of Eurasian autumn snow on the winter North Atlantic Oscillation in seasonal forecasts of the 20th century

Wegmann, Martin; Orsolini, Yvan J.; Weisheimer, Antje; Hurk, Bart Van Den; Lohmann, Gerrit

As the leading climate mode of wintertime climate variability over Europe, the North Atlantic Oscillation (NAO) has been extensively studied over the last decades. Recently, studies highlighted the state of the Eurasian cryosphere as a possible predictor for the wintertime NAO. However, missing correlation between snow cover and wintertime NAO in climate model experiments and strong non-stationarity of this link in reanalysis data are questioning the causality of this relationship.

Here we use the large ensemble of Atmospheric Seasonal Forecasts of the 20th Century (ASF-20C) with the European Centre for Medium-Range Weather Forecasts model, focusing on the winter season. Besides the main 110-year ensemble of 51 members, we investigate a second, perturbed ensemble of 21 members where initial (November) land conditions over the Northern Hemisphere are swapped from neighboring years. The Eurasian snow–NAO linkage is examined in terms of a longitudinal snow depth dipole across Eurasia. Subsampling the perturbed forecast ensemble and contrasting members with high and low initial snow dipole conditions, we found that their composite difference indicates more negative NAO states in the following winter (DJF) after positive west-to-east snow depth gradients at the beginning of November. Surface and atmospheric forecast anomalies through the troposphere and stratosphere associated with the anomalous positive snow dipole consist of colder early winter surface temperatures over eastern Eurasia, an enhanced Ural ridge and increased vertical energy fluxes into the stratosphere, with a subsequent negative NAO-like signature in the troposphere. We thus confirm the existence of a causal connection between autumn snow patterns and subsequent winter circulation in the ASF-20C forecasting system.

2021

Historical dry deposition of air pollution in the urban background in Oslo, Norway, compared to Western European data

Grøntoft, Terje

The historical (1835–2020) dry deposition of major air pollutants (SO2, NOx, O3 and PM2.5) in the urban background in Oslo, Norway, in a situation that could represent the building facades, was approximated from reported fuel combustion, emission factors, air concentrations since 1960, and dry deposition velocities. The annual accumulated dry deposition (and thus not considering the removal processes) of the pollutants, together, was found to have varied from about 2.3 to 27 g m−2, with the maximum in the 1960s caused by high SO2 emissions from the combustion of fuel oils, and with 1.6 kg m−2 having deposited over all the years. The deposition of PM2.5 was found to have dominated from 1835, have increased to a maximum in 1875 and then slowly decreased. The SO2 deposition decreased to a low value around 1990. The NOx deposition was also at its highest in the 1960s to about 1970, it became the largest from the 1980s, and then showed a clear decrease from about 2010. The O3 deposition was lower in the years of the maximum total and NOx deposition. The dry deposition of O3 and NOx were found to be about similar in 2020, more than two times that of PM2.5 and more than four times that of SO2. The trends of the NOx emissions were found to reflect the relative (1975) and absolute (∼2000) turning points of the environmental Kuznets curves (EKC) that has been suggested for Norway, whereas the trend of the SO2 emissions seems to have “shortcut” this development by the strong regulations in the emissions from 1970 that lead to near simultaneous relative and absolute reductions. The gradual decrease of the PM2.5 emissions from about 1945 seems to correspond with the decrease in combustion energy intensity in the economy as wood was substituted with more energy efficient fuels and then with the continued reduction in the wood burning.

2021

DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations

Niazi, Yasmeen; Thomsen, Hauke; Smolkova, Bozena; Vodickova, Ludmila; Vodenkova, Sona; Kroupa, Michal; Vymetalkova, Veronika; Kazimirova, Alena; Barancokova, Magdalena; Volkovova, Katarina; Staruchova, Marta; Hoffmann, Per; Nöthen, Markus M.; Dusinska, Maria; Musak, Ludovit; Vodicka, Pavel; Hemminki, Kari; Försti, Asta

DNA damage and unrepaired or insufficiently repaired DNA double-strand breaks as well as telomere shortening contribute to the formation of structural chromosomal aberrations (CAs). Non-specific CAs have been used in the monitoring of individuals exposed to potential carcinogenic chemicals and radiation. The frequency of CAs in peripheral blood lymphocytes (PBLs) has been associated with cancer risk and the association has also been found in incident cancer patients. CAs include chromosome-type aberrations (CSAs) and chromatid-type aberrations (CTAs) and their sum CAtot. In the present study, we used data from our published genome-wide association studies (GWASs) and extracted the results for 153 DNA repair genes for 607 persons who had occupational exposure to diverse harmful substances/radiation and/or personal exposure to tobacco smoking. The analyses were conducted using linear and logistic regression models to study the association of DNA repair gene polymorphisms with CAs. Considering an arbitrary cutoff level of 5 × 10–3, 14 loci passed the threshold, and included 7 repair pathways for CTA, 4 for CSA, and 3 for CAtot; 10 SNPs were eQTLs influencing the expression of the target repair gene. For the base excision repair pathway, the implicated genes PARP1 and PARP2 encode poly(ADP-ribosyl) transferases with multiple regulatory functions. PARP1 and PARP2 have an important role in maintaining genome stability through diverse mechanisms. Other candidate genes with known roles for CSAs included GTF2H (general transcription factor IIH subunits 4 and 5), Fanconi anemia pathway genes, and PMS2, a mismatch repair gene. The present results suggest pathways with mechanistic rationale for the formation of CAs and emphasize the need to further develop techniques for measuring individual sensitivity to genotoxic exposure.

2021

Transformative Potential and Learning Outcomes of Air Quality Citizen Science Projects in High Schools Using Low-Cost Sensors

Grossberndt, Sonja; Passani, Antonella; Lisio, Giulia Di; Janssen, Anneli; Castell, Nuria

The rise of advanced ICT technologies has made it possible to apply low-cost sensor systems for measuring air quality in citizen science projects, including education. High school students in Norway used these sensor systems in a citizen science project to design, carry out, and evaluate their own research projects on air quality. An impact assessment framework was designed to assess the impact of these activities, considering five areas of impact: scientific, social, economic, political, and environmental. In addition, the framework also considers the transformative potential of the citizen science pilot, i.e., the degree to which the pilot can help to change, alter, or replace current systems, and the business-as-usual in one or more fields such as knowledge production or environmental protection. Data for this assessment were gathered in the form of questionnaires that the students had to complete before starting and after finalizing the pilot activities. The results showed positive impacts on learning, a pro-environmental world view, and an increase in pro-science attitudes and interest in scientific and environmental-related topics at the end of the pilot activities. Only weak impacts were measured for behavioral change. The activities showed transformative potential, which makes the student activities an example of good practice for citizen science activities on air quality with low-cost sensors.

2021

How Atmospheric Chemistry and Transport Drive Surface Variability of N2O and CFC-11

Ruiz, Daniel J.; Prather, Michael J.; Strahan, Susan E.; Thompson, Rona Louise; Froidevaux, Lucien; Steenrod, Stephen D.

Nitrous oxide (N2O) is a long-lived greenhouse gas that affects atmospheric chemistry and climate. In this work, we use satellite measurements of N2O, ozone (O3), and temperature from the Aura Microwave Limb Sounder (MLS) instrument to calculate stratospheric loss of N2O, and thus its atmospheric lifetime. Using three chemistry transport models simulating the Aura period 2005–2017, we verify the stratospheric sink using MLS data and follow that loss signal down to the surface and compare with surface observations. Stratospheric loss has a strong seasonal cycle and is further modulated by the Quasi-Biennial Oscillation (QBO); these cycles are seen equally in both observations and the models. When filtered for interannual variability, the modeled surface signal is QBO-caused, and it reproduces the observed pattern, highlighting the potential role of the QBO in tropospheric chemistry and composition, as well as in model evaluation. The observed annual surface signal in the northern hemisphere matches well with the models run without emissions, indicating the annual cycle is driven mostly by stratosphere-troposphere exchange (STE) flux of N2O-depleted air and not surface N2O emissions. In the southern hemisphere (SH), all three models disagree and thus provide no guidance, except for indicating that modeling annual STE in the SH remains a major model uncertainty. Parallel model simulations of CFCl3, which has greater stratospheric loss that N2O and possibly surreptitious emissions, show that its interannual variations parallel those of N2O, and thus the observed N2O variability can identify the stratospheric component of the observed CFCl3 variability.

2021

The SCCS Notes of Guidance for the testing of cosmetic ingredients and their safety evaluation, 11th revision, 30–31 March 2021, SCCS/1628/21

Bernauer, Ulrike; Bodin, Laurent; Chaudhry, Qasim; Coenraads, Pieter Jan; Dusinska, Maria; Ezendam, Janine; Gaffet, Eric; Galli, Corrado Lodovico; Granum, Berit; Panteri, Eirini; Rogiers, Vera; Rousselle, Christophe; Stepnik, Maciej; Vanhaecke, Tamara; Wijnhoven, Susan

2021

Changes in black carbon emissions over Europe due to COVID-19 lockdowns

Evangeliou, Nikolaos; Platt, Stephen Matthew; Eckhardt, Sabine; Myhre, Cathrine Lund; Laj, Paolo; Alados-Arboledas, Lucas; Backman, John; Brem, Benjamin T.; Fiebig, Markus; Flentje, Harald; Marinoni, Angela; Pandolfi, Marco; Yus-Diez, Jesus; Prats, Natalia; Putaud, Jean-Philippe; Sellegri, Karine; Sorribas, Mar; Eleftheriadis, Konstantinos; Vratolis, Stergios; Wiedensohler, Alfred; Stohl, Andreas

Following the emergence of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) responsible for COVID-19 in December 2019 in Wuhan (China) and its spread to the rest of the world, the World Health Organization declared a global pandemic in March 2020. Without effective treatment in the initial pandemic phase, social distancing and mandatory quarantines were introduced as the only available preventative measure. In contrast to the detrimental societal impacts, air quality improved in all countries in which strict lockdowns were applied, due to lower pollutant emissions. Here we investigate the effects of the COVID-19 lockdowns in Europe on ambient black carbon (BC), which affects climate and damages health, using in situ observations from 17 European stations in a Bayesian inversion framework. BC emissions declined by 23 kt in Europe (20 % in Italy, 40 % in Germany, 34 % in Spain, 22 % in France) during lockdowns compared to the same period in the previous 5 years, which is partially attributed to COVID-19 measures. BC temporal variation in the countries enduring the most drastic restrictions showed the most distinct lockdown impacts. Increased particle light absorption in the beginning of the lockdown, confirmed by assimilated satellite and remote sensing data, suggests residential combustion was the dominant BC source. Accordingly, in central and Eastern Europe, which experienced lower than average temperatures, BC was elevated compared to the previous 5 years. Nevertheless, an average decrease of 11 % was seen for the whole of Europe compared to the start of the lockdown period, with the highest peaks in France (42 %), Germany (21 %), UK (13 %), Spain (11 %) and Italy (8 %). Such a decrease was not seen in the previous years, which also confirms the impact of COVID-19 on the European emissions of BC.

2021

Evaluation of novel cleaning systems on mock-ups of unvarnished oil paint and chalk-glue ground within the Munch Aula Paintings Project

Stoveland, Lena Porsmo; Frøysaker, Tine; Stols-Witlox, Maartje; Grøntoft, Terje; Steindal, Calin Constantin; Madden, Odile; Ormsby, Bronwyn

Low-risk removal of embedded surface soiling on delicate heritage objects can require novel alternatives to traditional cleaning systems. Edvard Munch’s monumental Aula paintings (1911–16) have a long history of exposure to atmospheric pollution and cleaning campaigns that have compromised the appearance and the condition of these important artworks. Soiling removal from porous and water-sensitive, unvarnished oil paintings continues to be a major conservation challenge. This paper presents the approach and results of research into the effect and efficiency of three novel systems used for soiling removal: soft particle blasting, CO2-snow blasting, and Nanorestore Gel® Dry and Peggy series hydrogels. Cleaning tests were performed on accelerated-aged and artificially soiled mock-ups consisting of unvarnished oil paint and chalk-glue grounds. Visual and analytical assessment (magnification using a light microscope and scanning electron microscope, as well as colour- and gloss measurement) was carried out before and after mock-up cleaning tests and the results were compared to those obtained using the dry polyurethane sponges employed in the most recent Aula surface cleaning campaign (2009–11). Although the results varied, the Nanorestore Gel® series proved promising with respect to improved soiling removal efficiency, and reduced pigment loss for the water-sensitive surfaces evaluated, compared to dry sponges.

2021

Assessing the impacts of citizen-led policies on emissions, air quality and health

Oliveira, Kevin; Rodrigues, Vera; Slingerland, Stephan; Vanherle, Kris; Soares, Joana; Rafael, Sandra; Trozzi, Carlo; Bouman, Evert; Ferreira, José Alexandre; Kewo, Angreine; Nielsen, Per Sieverts; Diafas, Iason; Monteiro, Alexandra; Miranda, Andreia I.; Lopes, Marta Júlia Marques; Hayes, Enda T.

Air pollution is a global challenge, and especially urban areas are particularly affected by acute episodes. Traditional approaches used to mitigate air pollution primarily consider the technical aspects of the problem but not the role of citizen behaviour and day-to-day practices. ClairCity, a Horizon 2020 funded project, created an impact assessment framework considering the role of citizen behaviour to create future scenarios, aiming to improve urban environments and the wellbeing and health of its inhabitants. This framework was applied to six pilot cases: Bristol, Amsterdam, Ljubljana, Sosnowiec, Aveiro Region and Liguria Region, considering three-time horizons: 2025, 2035 and 2050. The scenarios approach includes the Business As Usual (BAU) scenario and a Final Unified Policy Scenarios (FUPS) established by citizens, decision-makers, local planners and stakeholders based on data collected through a citizen and stakeholder co-creation process. Therefore, this paper aims to present the ClairCity outcomes, analysing the quantified impacts of selected measures in terms of emissions, air quality, population exposure, and health. Each case study has established a particular set of measures with different levels of ambition, therefore different levels of success were achieved towards the control and mitigation of their specific air pollution problems. The transport sector was the most addressed by the measures showing substantial improvements for NO2, already with the BAU scenarios, and overall, even better results when applying the citizen-led FUPS scenarios. In some cases, due to a lack of ambition for the residential and commercial sector, the results were not sufficient to fulfil the WHO guidelines. Overall, it was found in all cities that the co-created scenarios would lead to environmental improvements in terms of air quality and citizens’ health compared to the baseline year of 2015. However, in some cases, the health impacts were lower than air quality due to the implementation of the measures not affecting the most densely populated areas. Benefits from the FUPS comparing to the BAU scenario were found to be highest in Amsterdam and Bristol, with further NO2 and PM10 emission reductions around 10%–16% by 2025 and 19%–28% by 2050, compared to BAU.

2021

Global predictions of primary soil salinization under changing climate in the 21st century

Hassani, Amirhossein; Azapagic, Adisa; Shokri, Nima

Soil salinization has become one of the major environmental and socioeconomic issues globally and this is expected to be exacerbated further with projected climatic change. Determining how climate change influences the dynamics of naturally-occurring soil salinization has scarcely been addressed due to highly complex processes influencing salinization. This paper sets out to address this long-standing challenge by developing data-driven models capable of predicting primary (naturally-occurring) soil salinity and its variations in the world’s drylands up to the year 2100 under changing climate. Analysis of the future predictions made here identifies the dryland areas of South America, southern and western Australia, Mexico, southwest United States, and South Africa as the salinization hotspots. Conversely, we project a decrease in the soil salinity of the drylands in the northwest United States, the Horn of Africa, Eastern Europe, Turkmenistan, and west Kazakhstan in response to climate change over the same period.

2021

Brominated Flame Retardants in Antarctic Air in the Vicinity of Two All-Year Research Stations

Nash, Susan M. Bengtson; Wild, Seanan; Broomhall, Sara; Bohlin-Nizzetto, Pernilla

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.

2021

Clinical application of intrathecal gadobutrol for assessment of cerebrospinal fluid tracer clearance to blood

Eide, Per Kristian; Mariussen, Espen; Uggerud, Hilde Thelle; Pripp, Are Hugo; Lashkarivand, Aslan; Hassel, Bjørnar; Christensen, Hege Staaland; Hovd, Markus Herberg; Ringstad, Geir Andre

BACKGROUND. Methodology for estimation of cerebrospinal fluid (CSF) tracer clearance could have wide clinical application in predicting excretion of intrathecal drugs and metabolic solutes from brain metabolism and for diagnostic workup of CSF disturbances. METHODS. The MRI contrast agent gadobutrol (Gadovist) was used as a CSF tracer and injected into the lumbar CSF. Gadobutrol is contained outside blood vessels of the CNS and is eliminated along extravascular pathways, analogous to many CNS metabolites and intrathecal drugs. Tracer enrichment was verified and assessed in CSF by MRI at the level of the cisterna magna in parallel with obtaining blood samples through 48 hours. RESULTS. In a reference patient cohort (n = 29), both enrichment within CSF and blood coincided in time. Blood concentration profiles of gadobutrol through 48 hours varied between patients diagnosed with CSF leakage (n = 4), idiopathic normal pressure hydrocephalus dementia (n = 7), pineal cysts (n = 8), and idiopathic intracranial hypertension (n = 4). CONCLUSION. Assessment of CSF tracer clearance is clinically feasible and may provide a way to predict extravascular clearance of intrathecal drugs and endogenous metabolites from the CNS. The peak concentration in blood (at about 10 hours) was preceded by far peak tracer enhancement at MRI in extracranial lymphatic structures (at about 24 hours), as shown in previous studies, indicating a major role of the spinal canal in CSF clearance capacity. FUNDING. The work was supported by the Department of Neurosurgery, Oslo University Hospital; the Norwegian Institute for Air Research; and the University of Oslo.

2021

Validation of the Sentinel-5 Precursor TROPOMI cloud data withCloudnet, Aura OMI O2–O2, MODIS, and Suomi-NPP VIIR

Compernolle, Steven; Argyrouli, Athina; Lutz, Ronny; Sneep, Maarten; Lambert, Jean-Christopher; Fjæraa, Ann Mari; Hubert, Daan; Keppens, Arno; Loyola, Diego; O'Connor, Ewan; Romahn, Fabian; Stammes, Piet; Verhoelst, Tijl; Wang, Ping

Accurate knowledge of cloud properties is essential to the measurement of atmospheric composition from space. In this work we assess the quality of the cloud data from three Copernicus Sentinel-5 Precursor (S5P) TROPOMI cloud products: (i) S5P OCRA/ROCINN_CAL (Optical Cloud Recognition Algorithm/Retrieval of Cloud Information using Neural Networks;Clouds-As-Layers), (ii) S5P OCRA/ROCINN_CRB (Clouds-as-Reflecting Boundaries), and (iii) S5P FRESCO-S (Fast Retrieval Scheme for Clouds from Oxygen absorption bands – Sentinel). Target properties of this work are cloud-top height and cloud optical thickness (OCRA/ROCINN_CAL), cloud height (OCRA/ROCINN_CRB and FRESCO-S), and radiometric cloud fraction (all three algorithms). The analysis combines (i) the examination of cloud maps for artificial geographical patterns, (ii) the comparison to other satellite cloud data (MODIS, NPP-VIIRS, and OMI O2–O2), and (iii) ground-based validation with respect to correlative observations (30 April 2018 to 27 February 2020) from the Cloudnet network of ceilometers, lidars, and radars. Zonal mean latitudinal variation of S5P cloud properties is similar to that of other satellite data. S5P OCRA/ROCINN_CAL agrees well with NPP VIIRS cloud-top height and cloud optical thickness and with Cloudnet cloud-top height, especially for the low (mostly liquid) clouds. For the high clouds, S5P OCRA/ROCINN_CAL cloud-top height is below the cloud-top height of VIIRS and of Cloudnet, while its cloud optical thickness is higher than that of VIIRS. S5P OCRA/ROCINN_CRB and S5P FRESCO cloud height are well below the Cloudnet cloud mean height for the low clouds but match on average better with the Cloudnet cloud mean height for the higher clouds. As opposed to S5P OCRA/ROCINN_CRB and S5P FRESCO, S5P OCRA/ROCINN_CAL is well able to match the lowest CTH mode of the Cloudnet observations. Peculiar geographical patterns are identified in the cloud products and will be mitigated in future releases of the cloud data products.

2021

Hydrolysis of FTOH precursors, a simple method to account for some of the unknown PFAS

Nikiforov, Vladimir

There is a growing concern over a suspected presense of unknown perfluoroaliphatic substances (PFAS) in consumer goods and in the environment. Such unknown substances, possibly with high molecular weight, might be precursors of hazardous or controlled known PFAS. Recent studies confirmed that total organic fluorine (TOF) content often can not be explained by the measured target PFAS. One of the suspected classes of such unknowns are polymers with fluorotelomer alcohol (FTOH) residues in a side chain. In this report we suggest hydrolysis of precursors, as a complementary method to account for the unknown PFAS. It was shown here that hydrolysis allows to preserve structural information on the perlfuorinated parts of the precursors, which can be an advantage for the purpose of accurate risk assessment or source identification. A convenient procedure for hydrolysis with 4% sodium hydroxide inwater-methanol mixture (1:9) at 60 C for 16 h was shown to convert model substances - FTOH acrylate, methacrylate and isobutyrate esters as well as FTOH phenylcarbamate to free FTOHs. Analysis of extracts of textile samples with preliminary hydrolysis and without it showed up to 1300-fold higher level of “hidden” FTOHs.

2021

Maternal transfer and occurrence of siloxanes, chlorinated paraffins, metals, PFAS and legacy POPs in herring gulls (Larus argentatus) of different urban influence

Knudtzon, Nina C; Thorstensen, Helene; Ruus, Anders; Helberg, Morten; Bæk, Kine; Enge, Ellen Katrin; Borgå, Katrine

Urban herring gulls (Larus argentatus) are exposed to contaminants from aquatic, terrestrial and anthropogenic sources. We aim to assess if differences in urbanisation affect ecological niche and contaminant concentrations in female herring gulls. Furthermore, we investigated maternal transfer from mothers to eggs for all the target compounds, including chlorinated paraffins (CPs) and cyclic volatile methyl siloxane (cVMSs), which to our knowledge have not been assessed in herring gulls previously. We compare concentrations of legacy and emerging contaminants and metals in blood and eggs between two herring gull colonies located 51 km apart, in the urban influenced Norwegian Oslofjord. While both colonies are within an urbanised area, the inner fjord is more so, as it is surrounded by Oslo, the capital and largest city in Norway Stable isotopes of carbon and nitrogen indicated a more marine ecological niche in the outer than the inner fjord colony, although with overlap. Persistent organic pollutant (POP) concentrations were similar in the inner and outer fjord colonies, while the short-chained chlorinated paraffins (SCCP), which are recently added to the Stockholm convention and contaminants of emerging concern (CECs) varied, with higher concentrations of SCCP and the cVMS decamethylcyclopentasiloxane (D5) in females and eggs of the inner fjord colony. Per- and polyfluorinated substances (PFAS) concentrations were higher in the outer fjord colony, likely linked to releases from a point-source (airport and waste management facility with open access to food waste). In blood, chlorinated paraffins contributed most the total lipophilic contaminants (inner: 78%, outer: 56%), while polychlorinated biphenyls (PCBs) were the most abundant lipophilic contaminants in eggs (inner: 62%, outer: 46%). Dechloranes and brominated flame retardants (BFRs) were detected in few samples. Maternal transfer, assessed by egg to blood ratios, of cVMSs were similar to the POPs with mean log ratio 0.39 (D5), while it was lower for SCCPs, with log ratios-0.77. Our results indicate comparable POP exposure of the herring gulls in the inner and outer Oslofjord, likely due to overlap in ecological niches between the colonies and wide distribution of POPs. The differences between the colonies in concentrations of PFAS, cVMS and CPs shows that point source exposures and urban influence may be more important than ecological niche for these compounds.

2021

Trends, composition, and sources of carbonaceous aerosol at the Birkenes Observatory, northern Europe, 2001–2018

Yttri, Karl Espen; Canonaco, Francesco; Eckhardt, Sabine; Evangeliou, Nikolaos; Fiebig, Markus; Gundersen, Hans; Hjellbrekke, Anne-Gunn; Myhre, Cathrine Lund; Platt, Stephen Matthew; Prévôt, André S. H.; Simpson, David; Solberg, Sverre; Surratt, Jason D.; Tørseth, Kjetil; Uggerud, Hilde Thelle; Vadset, Marit; Wan, Xin; Aas, Wenche

We present 18 years (2001–2018) of aerosol measurements, including organic and elemental carbon (OC andEC), organic tracers (levoglucosan, arabitol, mannitol, trehalose, glucose, and 2-methyltetrols), trace elements, andions, at the Birkenes Observatory (southern Norway) – a site representative of the northern European region. The OC/EC (2001–2018) and the levoglucosan (2008–2018) time series are the longest in Europe, with OC/EC available for the PM10, PM2.5 (fine), and PM10–2.5 (coarse) size fractions, providing the opportunity for a nearly 2-decade-long assessment. Using positive matrix factorization (PMF), we identify seven carbonaceous aerosol sources at Birkenes: mineral-dust-dominated aerosol (MIN), traffic/industry-like aerosol (TRA/IND), short-range-transported biogenic secondary organic aerosol (BSOASRT), primary biological aerosol particles (PBAP), biomass burning aerosol (BB), ammonium-nitrate-dominated aerosol (NH4NO3), and (one low carbon fraction) sea salt aerosol (SS).
We observed significant (p < 0.05), large decreases in EC in PM10 (−3.9 % yr−1) and PM2.5 (−4.2 % yr−1) anda smaller decline in levoglucosan (−2.8 % yr−1), suggesting that OC/EC from traffic and industry is decreasing, whereas the abatement of OC/EC from biomass burning has beenslightly less successful. EC abatement with respect to anthropogenic sources is further supported by decreasing EC fractions in PM2.5 (−3.9 % yr−1) and PM10(−4.5 % yr−1).
PMF apportioned 72 % of EC to fossil fuel sources; this was further supported by PMF applied to absorption photometer data, which yielded a two-factor solution with alow aerosol Ångstrøm exponent (AAE=0.93) fraction, as-sumed to be equivalent black carbon from fossil fuel combustion (eBCFF), contributing 78 % to eBC mass. The higher AAE fraction (AAE=2.04) is likely eBC from BB (eBCBB). Source–receptor model calculations (FLEXPART) showed that continental Europe and western Russia were the main source regions of both elevated eBCBB and eBCFF.
Dominating biogenic sources explain why there was no downward trend for OC. A relative increase in the OC fraction in PM2.5(+3.2 % yr−1) and PM10(+2.4 % yr−1) underscores the importance of biogenic sources at Birkene (BSOA and PBAP), which were higher in the vegetative season and dominated both fine (53 %) and coarse (78 %) OC. Furthermore, 77 %–91 % of OC in PM2.5, PM10–2.5, and PM10 was attributed to biogenic sources in summer vs. 22 %–37 % in winter. The coarse fraction had the highest share of biogenic sources regardless of season and was dominated by PBAP, except in winter. Our results show a shift in the aerosol composition at Birkenes and, thus, also in the relative source contributions. The need for diverse offline and online carbonaceous aerosol speciation to understand carbonaceous aerosol sources, including their seasonal, annual, and long-term variability, has been demonstrated.

2021

AeroCom phase III multi-model evaluation of the aerosol life cycle and optical properties using ground- and space-based remote sensing as well as surface in situ observations

Gliss, Jonas; Mortier, Augustin; Schulz, Michael; Andrews, Elisabeth; Balkanski, Yves; Bauer, Susanne E.; Benedictow, Anna Maria Katarina; Bian, Huisheng; Checa-Garcia, Ramiro; Chin, Mian; Ginoux, Paul; Griesfeller, Jan; Heckel, Andreas; Kipling, Zak; Kirkevåg, Alf; Kokkola, Harri; Laj, Paolo G.; Sager, Philippe Le; Lund, Marianne Tronstad; Myhre, Cathrine Lund; Matsui, Hitoshi; Myhre, Gunnar; Neubauer, David; Noije, Twan van; North, Peter; Oliviè, Dirk Jan Leo; Remy, Samuel; Sogacheva, Larisa; Takemura, Toshihiko; Tsigaridis, Kostas; Tsyro, Svetlana

Within the framework of the AeroCom (Aerosol Comparisons between Observations and Models) initiative, the state-of-the-art modelling of aerosol optical properties is assessed from 14 global models participating in the phase III control experiment (AP3). The models are similar to CMIP6/AerChemMIP Earth System Models (ESMs) and provide a robust multi-model ensemble. Inter-model spread of aerosol species lifetimes and emissions appears to be similar to that of mass extinction coefficients (MECs), suggesting that aerosol optical depth (AOD) uncertainties are associated with a broad spectrum of parameterised aerosol processes.
Total AOD is approximately the same as in AeroCom phase I (AP1) simulations. However, we find a 50 % decrease in the optical depth (OD) of black carbon (BC), attributable to a combination of decreased emissions and lifetimes. Relative contributions from sea salt (SS) and dust (DU) have shifted from being approximately equal in AP1 to SS contributing about 2∕3 of the natural AOD in AP3. This shift is linked with a decrease in DU mass burden, a lower DU MEC, and a slight decrease in DU lifetime, suggesting coarser DU particle sizes in AP3 compared to AP1.
Relative to observations, the AP3 ensemble median and most of the participating models underestimate all aerosol optical properties investigated, that is, total AOD as well as fine and coarse AOD (AODf, AODc), Ångström exponent (AE), dry surface scattering (SCdry), and absorption (ACdry) coefficients. Compared to AERONET, the models underestimate total AOD by ca. 21 % ± 20 % (as inferred from the ensemble median and interquartile range). Against satellite data, the ensemble AOD biases range from −37 % (MODIS-Terra) to −16 % (MERGED-FMI, a multi-satellite AOD product), which we explain by differences between individual satellites and AERONET measurements themselves. Correlation coefficients (R) between model and observation AOD records are generally high (R>0.75), suggesting that the models are capable of capturing spatio-temporal variations in AOD. We find a much larger underestimate in coarse AODc (∼ −45 % ± 25 %) than in fine AODf (∼ −15 % ± 25 %) with slightly increased inter-model spread compared to total AOD. These results indicate problems in the modelling of DU and SS. The AODc bias is likely due to missing DU over continental land masses (particularly over the United States, SE Asia, and S. America), while marine AERONET sites and the AATSR SU satellite data suggest more moderate oceanic biases in AODc.
Column AEs are underestimated by about 10 % ± 16 %. For situations in which measurements show AE > 2, models underestimate AERONET AE by ca. 35 %. In contrast, all models (but one) exhibit large overestimates in AE when coarse aerosol dominates (bias ca. +140 % if observed AE < 0.5). Simulated AE does not span the observed AE variability. These results indicate that models overestimate particle size (or underestimate the fine-mode fraction) for fine-dominated aerosol and underestimate size (or overestimate the fine-mode fraction) for coarse-dominated aerosol. This must have implications for lifetime, water uptake, scattering enhancement, and the aerosol radiative effect, which we can not quantify at this moment.
Comparison against Global Atmosphere Watch (GAW) in situ data results in mean bias and inter-model variations of −35 % ± 25 % and −20 % ± 18 % for SCdry and ACdry, respectively. The larger underestimate of SCdry than ACdry suggests the models will simulate an aerosol single scattering albedo that is too low. The larger underestimate of SCdry than ambient air AOD is consistent with recent findings that models overestimate scattering enhancement due to hygroscopic growth. The broadly consistent negative bias in AOD and surface scattering suggests an underestimate of aerosol radiative effects in current global aerosol models.
Considerable ...

2021

Evaluation and optimization of ICOS atmosphere station data as part of the labeling process

Yver-Kwok, Camille; Philippon, Camille; Bergamaschi, Peter; Biermann, Tobias; Calzolari, Francescopiero; Chen, Huilin; Conil, Sébastien; Cristofanelli, Paolo; Delmotte, Marc; Hatakka, Juha; Heliasz, Michal; Hermansen, Ove; Kominkova, Katerina; Kubistin, Dagmar; Kumps, Nicolas; Laurent, Olivier; Laurila, Tuomas; Lehner, Irene; Levula, Janne; Lindauer, Matthias; Lopez, Morgan; Mammarella, Ivan; Manca, Giovanni; Marklund, Per; Metzger, Jean-Marc; Mölder, Meelis; Platt, Stephen Matthew; Ramonet, Michel; Rivier, Leonard; Scheeren, Bert; Sha, Mahesh Kumar; Smith, Paul; Steinbacher, Martin; Vitkova, Gabriela; Wyss, Simon

The Integrated Carbon Observation System (ICOS) is a pan-European research infrastructure which provides harmonized and high-precision scientific data on the carbon cycle and the greenhouse gas budget. All stations have to undergo a rigorous assessment before being labeled, i.e., receiving approval to join the network. In this paper, we present the labeling process for the ICOS atmosphere network through the 23 stations that were labeled between November 2017 and November 2019. We describe the labeling steps, as well as the quality controls, used to verify that the ICOS data (CO2, CH4, CO and meteorological measurements) attain the expected quality level defined within ICOS. To ensure the quality of the greenhouse gas data, three to four calibration gases and two target gases are measured: one target two to three times a day, the other gases twice a month. The data are verified on a weekly basis, and tests on the station sampling lines are performed twice a year. From these high-quality data, we conclude that regular calibrations of the CO2, CH4 and CO analyzers used here (twice a month) are important in particular for carbon monoxide (CO) due to the analyzer's variability and that reducing the number of calibration injections (from four to three) in a calibration sequence is possible, saving gas and extending the calibration gas lifespan. We also show that currently, the on-site water vapor correction test does not deliver quantitative results possibly due to environmental factors. Thus the use of a drying system is strongly recommended. Finally, the mandatory regular intake line tests are shown to be useful in detecting artifacts and leaks, as shown here via three different examples at the stations.

2021

Quantifying the Impact of the Covid-19 Lockdown Measures on Nitrogen Dioxide Levels throughout Europe

Solberg, Sverre; Walker, Sam-Erik; Schneider, Philipp; Guerreiro, Cristina

In this paper, the effect of the lockdown measures on nitrogen dioxide (NO2) in Europe is analysed by a statistical model approach based on a generalised additive model (GAM). The GAM is designed to find relationships between various meteorological parameters and temporal metrics (day of week, season, etc.) on the one hand and the level of pollutants on the other. The model is first trained on measurement data from almost 2000 monitoring stations during 2015–2019 and then applied to the same stations in 2020, providing predictions of expected concentrations in the absence of a lockdown. The difference between the modelled levels and the actual measurements from 2020 is used to calculate the impact of the lockdown measures adjusted for confounding effects, such as meteorology and temporal trends. The study is focused on April 2020, the month with the strongest reductions in NO2, as well as on the gradual recovery until the end of July. Significant differences between the countries are identified, with the largest NO2 reductions in Spain, France, Italy, Great Britain and Portugal and the smallest in eastern countries (Poland and Hungary). The model is found to perform best for urban and suburban sites. A comparison between the found relative changes in urban surface NO2 data during the lockdown and the corresponding changes in tropospheric vertical NO2 column density as observed by the TROPOMI instrument on Sentinel-5P revealed good agreement despite substantial differences in the observing method.

2021

Microfluidic In Vitro Platform for (Nano)Safety and (Nano)Drug Efficiency Screening

Kohl, Yvonne; Biehl, Margit; Spring, Sarah; Hesler, Michelle; Ogourtsov, Vladimir; Todorovic, Miomir; Owen, Joshua; Elje, Elisabeth; Kopecka, Kristina; Moriones, Oscar Hernando; Bastus, Neus G.; Simon, Peter; Dubaj, Tibor; Rundén-Pran, Elise; Puntes, Victor; William, Nicola; Briesen, Hagen von; Wagner, Sylvia; Kapur, Nikil; Mariussen, Espen; Nelson, Andrew; Gabelova, A; Dusinska, Maria; Velten, Thomas; Knoll, Thorsten

Microfluidic technology is a valuable tool for realizing more in vitro models capturing cellular and organ level responses for rapid and animal‐free risk assessment of new chemicals and drugs. Microfluidic cell‐based devices allow high‐throughput screening and flexible automation while lowering costs and reagent consumption due to their miniaturization. There is a growing need for faster and animal‐free approaches for drug development and safety assessment of chemicals (Registration, Evaluation, Authorisation and Restriction of Chemical Substances, REACH). The work presented describes a microfluidic platform for in vivo‐like in vitro cell cultivation. It is equipped with a wafer‐based silicon chip including integrated electrodes and a microcavity. A proof‐of‐concept using different relevant cell models shows its suitability for label‐free assessment of cytotoxic effects. A miniaturized microscope within each module monitors cell morphology and proliferation. Electrodes integrated in the microfluidic channels allow the noninvasive monitoring of barrier integrity followed by a label‐free assessment of cytotoxic effects. Each microfluidic cell cultivation module can be operated individually or be interconnected in a flexible way. The interconnection of the different modules aims at simulation of the whole‐body exposure and response and can contribute to the replacement of animal testing in risk assessment studies in compliance with the 3Rs to replace, reduce, and refine animal experiments.

2021

Non-target and suspect characterisation of organic contaminants in ambient air, Part I: Combining a novel sample clean-up method with comprehensive two-dimensional gas chromatography

Röhler, Laura; Bohlin-Nizzetto, Pernilla; Rostkowski, Pawel; Kallenborn, Roland; Schlabach, Martin

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

DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population

Niazi, Yasmeen; Thomsen, Hauke; Smolkova, Bozena; Vodickova, Ludmila; Vodenkova, Sona; Kroupa, Michal; Vymetalkova, Veronika; Kazimirova, Alena; Barancokova, Magdalena; Volkovova, Katarina; Staruchova, Marta; Hoffmann, Per; Nöthen, Markus M; Dusinska, Maria; Musak, Ludovit; Vodicka, Pavel; Försti, Asta; Hemminki, Kari

2021

Real-time measurement of radionuclide concentrations and its impact on inverse modeling of 106Ru release in the fall of 2017

Tichý, Ondřej; Hýza, Miroslav; Evangeliou, Nikolaos; Šmídl, Václav

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

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