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Found 2647 publications. Showing page 41 of 265:

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Odds and ends of atmospheric mercury in Europe and over the North Atlantic Ocean: temporal trends of 25 years of measurements

Custódio, Danilo; Pfaffhuber, Katrine Aspmo; Spain, T. Gerard; Pankratov, Fidel F.; Strigunova, Iana; Molepo, Koketso; Skov, Henrik; Bieser, Johannes; Ebinghaus, Ralf

The global monitoring plan of the Minamata Convention on Mercury was established to generate long-term data necessary for evaluating the effectiveness of regulatory measures at a global scale. After 25 years of monitoring (since 1995), Mace Head is one of the atmospheric monitoring stations with the longest mercury record and has produced sufficient data for the analysis of temporal trends of total gaseous mercury (TGM) in Europe and the North Atlantic. Using concentration-weighted trajectories for atmospheric mercury measured at Mace Head as well as another five locations in Europe, Amderma, Andøya, Villum, Waldhof and Zeppelin, we identify the regional probabilistic source contribution factor and its changes for the period of 1996 to 2019. Temporal trends indicate that concentrations of mercury in the atmosphere in Europe and the North Atlantic have declined significantly over the past 25 years at a non-monotonic rate averaging 0.03  . Concentrations of TGM at remote marine sites were shown to be affected by continental long-range transport, and evaluation of reanalysis back trajectories displays a significant decrease in TGM in continental air masses from Europe in the last 2 decades. In addition, using the relationship between mercury and other atmospheric trace gases that could serve as a source signature, we perform factorization regression analysis, based on positive rotatable factorization to solve probabilistic mass functions. We reconstructed atmospheric mercury concentration and assessed the contribution of the major natural and anthropogenic sources. The results reveal that the observed downward trend in the atmospheric mercury is mainly associated with a factor with a high load of long-lived anthropogenic species.

2022

Development of a Novel Framework for the Assessment and Improvement of Climate Adaptation and Mitigation Actions in Europe

Ottaviani Aalmo, Giovanna; Gioli, Beniamino; Rodriguez, Divina Gracia P.; Tuomasjukka, Diana; Liu, Hai-Ying; Pastore, Maria Chiara; Salbitano, Fabio; Bogetoft, Peter; Sæbø, Arne; Konijnendijk, Cecil

The greenhouse gases (GHG) emissions in the European Union (EU) are mainly caused by human activity from five sectors—power, industry, transport, buildings, and agriculture. To tackle all these challenges, the EU actions and policies have been encouraging initiatives focusing on a holistic approach but these initiatives are not enough coordinated and connected to reach the much needed impact. To strengthen the important role of regions in climate actions, and stimulate wide stakeholders’ engagement including citizens, a conceptual framework for enabling rapid and far-reaching climate actions through multi-sectoral regional adaptation pathways is hereby developed. The target audience for this framework is composed by regional policy makers, developers and fellow scientists. The scale of the framework emphasizes the regional function as an important meeting point and delivery arena for European and national climate strategies and objectives both at urban and rural level. The framework is based on transformative and no-regret measures, prioritizing the Key Community Systems (KCS) that most urgently need to be protected from climate impacts and risks.

Frontiers Media S.A.

2022

What caused a record high PM10 episode in northern Europe in October 2020?

Zwaaftink, Christine Groot; Aas, Wenche; Eckhardt, Sabine; Evangeliou, Nikolaos; Hamer, Paul David; Johnsrud, Mona; Kylling, Arve; Platt, Stephen Matthew; Stebel, Kerstin; Uggerud, Hilde Thelle; Yttri, Karl Espen

In early October 2020, northern Europe experienced an episode with poor air quality due to high concentrations of particulate matter (PM). At several sites in Norway, recorded weekly values exceeded historical maximum PM10 concentrations from the past 4 to 10 years. Daily mean PM10 values at Norwegian sites were up to 97 µg m−3 and had a median value of 59 µg m−3. We analysed this severe pollution episode caused by long-range atmospheric transport based on surface and remote sensing observations and transport model simulations to understand its causes. Samples from three sites in mainland Norway and the Arctic remote station Zeppelin (Svalbard) showed strong contributions from mineral dust to PM10 (23 %–36 % as a minimum and 31 %–45 % as a maximum) and biomass burning (8 %–16 % to 19 %–21 %). Atmospheric transport simulations indicate that Central Asia was the main source region for mineral dust observed in this episode. The biomass burning fraction can be attributed to forest fires in Ukraine and southern Russia, but we cannot exclude other sources contributing, like fires elsewhere, because the model underestimates observed concentrations. The combined use of remote sensing, surface measurements, and transport modelling proved effective in describing the episode and distinguishing its causes.

2022

Mass Cultivation of Microalgae: I. Experiences with Vertical Column Airlift Photobioreactors, Diatoms and CO2 Sequestration

Eilertsen, Hans Christian; Eriksen, Gunilla; Bergum, John-Steinar; Strømholt, Jo; Elvevoll, Edel O.; Eilertsen, Karl-Erik; Heimstad, Eldbjørg Sofie; Giæver, Ingeborg Hulda; Israelsen, Linn; Svenning, Jon Brage; Dalheim, Lars; Osvik, Renate Døving; Hansen, Espen Holst; Ingebrigtsen, Richard Andre; Aspen, Terje M; Wintervoll, Geir-Henning

From 2015 to 2021, we optimized mass cultivation of diatoms in our own developed vertical column airlift photobioreactors using natural and artificial light (LEDs). The project took place at the ferrosilicon producer Finnfjord AS in North Norway as a joint venture with UiT—The Arctic University of Norway. Small (0.1–6–14 m3) reactors were used for initial experiments and to produce inoculum cultures while upscaling experiments took place in a 300 m3 reactor. We here argue that species cultivated in reactors should be large since biovolume specific self-shadowing of light can be lower for large vs. small cells. The highest production, 1.28 cm3 L−1 biovolume (0.09–0.31 g DW day−1), was obtained with continuous culture at ca. 19% light utilization efficiency and 34% CO2 uptake. We cultivated 4–6 months without microbial contamination or biofouling, and this we argue was due to a natural antifouling (anti-biofilm) agent in the algae. In terms of protein quality all essential amino acids were present, and the composition and digestibility of the fatty acids were as required for feed ingredients. Lipid content was ca. 20% of ash-free DW with high EPA levels, and omega-3 and amino acid content increased when factory fume was added. The content of heavy metals in algae cultivated with fume was well within the accepted safety limits. Organic pollutants (e.g., dioxins and PCBs) were below the limits required by the European Union food safety regulations, and bioprospecting revealed several promising findings.

MDPI

2022

Impact of 3D cloud structures on the atmospheric trace gas products from UV–Vis sounders – Part 1: Synthetic dataset for validation of trace gas retrieval algorithms

Emde, Claudia; Yu, Huan; Kylling, Arve; Van Roozendael, Michel; Stebel, Kerstin; Veihelmann, Ben

Retrievals of trace gas concentrations from satellite observations are mostly performed for clear regions or regions with low cloud coverage. However, even fully clear pixels can be affected by clouds in the vicinity, either by shadowing or by scattering of radiation from clouds in the clear region. Quantifying the error of retrieved trace gas concentrations due to cloud scattering is a difficult task. One possibility is to generate synthetic data by three-dimensional (3D) radiative transfer simulations using realistic 3D atmospheric input data, including 3D cloud structures. Retrieval algorithms may be applied on the synthetic data, and comparison to the known input trace gas concentrations yields the retrieval error due to cloud scattering.

In this paper we present a comprehensive synthetic dataset which has been generated using the Monte Carlo radiative transfer model MYSTIC (Monte Carlo code for the phYSically correct Tracing of photons In Cloudy atmospheres). The dataset includes simulated spectra in two spectral ranges (400–500 nm and the O2A-band from 755–775 nm). Moreover it includes layer air mass factors (layer-AMFs) calculated at 460 nm. All simulations are performed for a fixed background atmosphere for various sun positions, viewing directions and surface albedos.

Two cloud setups are considered: the first includes simple box clouds with various geometrical and optical thicknesses. This can be used to systematically investigate the sensitivity of the retrieval error on solar zenith angle, surface albedo and cloud parameters. Corresponding 1D simulations are also provided. The second includes realistic three-dimensional clouds from an ICON large eddy simulation (LES) for a region covering Germany and parts of surrounding countries. The scene includes cloud types typical of central Europe such as shallow cumulus, convective cloud cells, cirrus and stratocumulus. This large dataset can be used to quantify the trace gas concentration retrieval error statistically.

Along with the dataset, the impact of horizontal photon transport on reflectance spectra and layer-AMFs is analysed for the box-cloud scenarios. Moreover, the impact of 3D cloud scattering on the NO2 vertical column density (VCD) retrieval is presented for a specific LES case. We find that the retrieval error is largest in cloud shadow regions, where the NO2 VCD is underestimated by more than 20 %.

The dataset is available for the scientific community to assess the behaviour of trace gas retrieval algorithms and cloud correction schemes in cloud conditions with 3D structure.

2022

Atmospheric composition in the European Arctic and 30 years of the Zeppelin Observatory, Ny-Ålesund

Platt, Stephen Matthew; Hov, Øystein; Berg, Torunn; Breivik, Knut; Eckhardt, Sabine; Eleftheriadis, Konstantinos; Evangeliou, Nikolaos; Fiebig, Markus; Fisher, Rebecca; Hansen, Georg Heinrich; Hansson, Hans-Christen; Heintzenberg, Jost; Hermansen, Ove; Heslin-Rees, Dominic; Holmén, Kim; Hudson, Stephen; Kallenborn, Roland; Krejci, Radovan; Krognes, Terje; Larssen, Steinar; Lowry, David; Myhre, Cathrine Lund; Lunder, Chris Rene; Nisbet, Euan; Bohlin-Nizzetto, Pernilla; Park, Ki-Tae; Pedersen, Christina Alsvik; Pfaffhuber, Katrine Aspmo; Röckmann, Thomas; Schmidbauer, Norbert; Solberg, Sverre; Stohl, Andreas; Ström, Johan; Svendby, Tove Marit; Tunved, Peter; Tørnkvist, Kjersti Karlsen; van der Veen, Carina; Vratolis, Stergios; Jun Yoon, Young; Yttri, Karl Espen; Zieger, Paul; Aas, Wenche; Tørseth, Kjetil

The Zeppelin Observatory (78.90∘ N, 11.88∘ E) is located on Zeppelin Mountain at 472 m a.s.l. on Spitsbergen, the largest island of the Svalbard archipelago. Established in 1989, the observatory is part of Ny-Ålesund Research Station and an important atmospheric measurement site, one of only a few in the high Arctic, and a part of several European and global monitoring programmes and research infrastructures, notably the European Monitoring and Evaluation Programme (EMEP); the Arctic Monitoring and Assessment Programme (AMAP); the Global Atmosphere Watch (GAW); the Aerosol, Clouds and Trace Gases Research Infrastructure (ACTRIS); the Advanced Global Atmospheric Gases Experiment (AGAGE) network; and the Integrated Carbon Observation System (ICOS). The observatory is jointly operated by the Norwegian Polar Institute (NPI), Stockholm University, and the Norwegian Institute for Air Research (NILU). Here we detail the establishment of the Zeppelin Observatory including historical measurements of atmospheric composition in the European Arctic leading to its construction. We present a history of the measurements at the observatory and review the current state of the European Arctic atmosphere, including results from trends in greenhouse gases, chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs), other traces gases, persistent organic pollutants (POPs) and heavy metals, aerosols and Arctic haze, and atmospheric transport phenomena, and provide an outline of future research directions.

2022

Sources and fate of atmospheric microplastics revealed from inverse and dispersion modelling: From global emissions to deposition

Evangeliou, Nikolaos; Tichý, Ondřej; Eckhardt, Sabine; Zwaaftink, Christine Groot; Brahney, Janice

We combine observations from Western USA and inverse modelling to constrain global atmospheric emissions of microplastics (MPs) and microfibers (MFs). The latter are used further to model their global atmospheric dynamics. Global annual MP emissions were calculated as 9.6 ± 3.6 Tg and MF emissions as 6.5 ± 2.9 Tg. Global average monthly MP concentrations were 47 ng m-3 and 33 ng m-3 for MFs, at maximum. The largest deposition of agricultural MPs occurred close to the world’s largest agricultural regions. Road MPs mostly deposited in the East Coast of USA, Central Europe, and Southeastern Asia; MPs resuspended with mineral dust near Sahara and Middle East. Only 1.8% of the emitted mass of oceanic MPs was transferred to land, and 1.4% of land MPs to ocean; the rest were deposited in the same environment. Previous studies reported that 0.74–1.9 Tg y-1 of land-based atmospheric MPs/MFs (

Elsevier

2022

Elucidating the present-day chemical composition, seasonality and source regions of climate-relevant aerosols across the Arctic land surface

Moschos, Vaios; Schmale, Julia; Aas, Wenche; Becagli, Silvia; Calzolai, Giulia; Eleftheriadis, Konstantinos; Moffett, Claire E.; Schnelle-Kreis, Jürgen; Severi, Mirko; Sharma, Sangeeta; Skov, Henrik; Vestenius, Mika; Zhang, Wendy; Hakola, Hannele; Hellén, Heidi; Huang, Lin; Jaffrezo, Jean-Luc; Massling, Andreas; Nøjgaard, Jacob Klenø; Petäjä, Tuukka; Popovicheva, Olga; Sheesley, Rebecca J.; Traversi, Rita; Yttri, Karl Espen; Prévôt, André S. H.; Baltensperger, Urs; El Haddad, Imad

The Arctic is warming two to three times faster than the global average, and the role of aerosols is not well constrained. Aerosol number concentrations can be very low in remote environments, rendering local cloud radiative properties highly sensitive to available aerosol. The composition and sources of the climate-relevant aerosols, affecting Arctic cloud formation and altering their microphysics, remain largely elusive due to a lack of harmonized concurrent multi-component, multi-site, and multi-season observations. Here, we present a dataset on the overall chemical composition and seasonal variability of the Arctic total particulate matter (with a size cut at 10 μm, PM10, or without any size cut) at eight observatories representing all Arctic sectors. Our holistic observational approach includes the Russian Arctic, a significant emission source area with less dedicated aerosol monitoring, and extends beyond the more traditionally studied summer period and black carbon/sulfate or fine-mode pollutants. The major airborne Arctic PM components in terms of dry mass are sea salt, secondary (non-sea-salt, nss) sulfate, and organic aerosol (OA), with minor contributions from elemental carbon (EC) and ammonium. We observe substantial spatiotemporal variability in component ratios, such as EC/OA, ammonium/nss-sulfate and OA/nss-sulfate, and fractional contributions to PM. When combined with component-specific back-trajectory analysis to identify marine or terrestrial origins, as well as the companion study by Moschos et al 2022 Nat. Geosci. focusing on OA, the composition analysis provides policy-guiding observational insights into sector-based differences in natural and anthropogenic Arctic aerosol sources. In this regard, we first reveal major source regions of inner-Arctic sea salt, biogenic sulfate, and natural organics, and highlight an underappreciated wintertime source of primary carbonaceous aerosols (EC and OA) in West Siberia, potentially associated with the oil and gas sector. The presented dataset can assist in reducing uncertainties in modelling pan-Arctic aerosol-climate interactions, as the major contributors to yearly aerosol mass can be constrained. These models can then be used to predict the future evolution of individual inner-Arctic atmospheric PM components in light of current and emerging pollution mitigation measures and improved region-specific emission inventories.

2022

Equal abundance of summertime natural and wintertime anthropogenic Arctic organic aerosols

Moschos, Vaios; Dzepina, Katja; Bhattu, Deepika; Lamkaddam, Houssni; Casotto, Roberto; Daellenbach, Kaspar R.; Canonaco, Francesco; Rai, Pragati; Aas, Wenche; Becagli, Silvia; Calzolai, Giulia; Eleftheriadis, Konstantinos; Moffett, Claire E.; Schnelle-Kreis, Jürgen; Seviri, Mirko; Sharma, Sangeeta; Skov, Henrik; Vestenius, Mika; Zhang, Wendy; Hakola, Hannele; Hellén, Heidi; Huang, Lin; Jaffrezo, Jean-Luc; Massling, Andreas; Nøjgaard, Jacob Klenø; Petäjä, Tuukka; Popovicheva, Olga; Sheesley, Rebecca J.; Traversi, Rita; Yttri, Karl Espen; Schmale, Julia; Prévôt, André S. H.; Baltensperger, Urs; El Haddad, Imad

Aerosols play an important yet uncertain role in modulating the radiation balance of the sensitive Arctic atmosphere. Organic aerosol is one of the most abundant, yet least understood, fractions of the Arctic aerosol mass. Here we use data from eight observatories that represent the entire Arctic to reveal the annual cycles in anthropogenic and biogenic sources of organic aerosol. We show that during winter, the organic aerosol in the Arctic is dominated by anthropogenic emissions, mainly from Eurasia, which consist of both direct combustion emissions and long-range transported, aged pollution. In summer, the decreasing anthropogenic pollution is replaced by natural emissions. These include marine secondary, biogenic secondary and primary biological emissions, which have the potential to be important to Arctic climate by modifying the cloud condensation nuclei properties and acting as ice-nucleating particles. Their source strength or atmospheric processing is sensitive to nutrient availability, solar radiation, temperature and snow cover. Our results provide a comprehensive understanding of the current pan-Arctic organic aerosol, which can be used to support modelling efforts that aim to quantify the climate impacts of emissions in this sensitive region.

2022

The influence of photochemistry on outdoor to indoor NO2 in some European museums

Grøntoft, Terje

This paper reports 1 year of monthly average NO2 indoor to outdoor (I/O) concentrations measured in 10 European museums, and a simple steady-state box model that explains the annual variation. The measurements were performed in the EU FP5 project Master (EVK-CT-2002-00093). The work provides extensive documentation of the annual variation of NO2 I/O concentration ratios, with ratios above unity in the summer, in situations with no indoor emissions of NO2. The modelling included the most relevant production and removal processes of NO2 and showed that the outdoor photolysis was the probable main explanation of the annual trends in the NO2 I/O concentration ratios.

John Wiley & Sons

2022

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