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Opinion: New directions in atmospheric research offered by research infrastructures combined with open and data-intensive science

Petzold, Andreas; Bundke, Ulrich; Hienola, Anca; Laj, Paolo; Myhre, Cathrine Lund; Vermeulen, Alex; Adamaki, Angeliki; Kutsch, Werner; Thouret, Valerie; Boulanger, Damien; Fiebig, Markus; Stocker, Markus; Zhao, Zhiming; Asmi, Ari

The acquisition and dissemination of essential information for understanding global biogeochemical interactions between the atmosphere and ecosystems and how climate–ecosystem feedback loops may change atmospheric composition in the future comprise a fundamental prerequisite for societal resilience in the face of climate change. In particular, the detection of trends and seasonality in the abundance of greenhouse gases and short-lived climate-active atmospheric constituents is an important aspect of climate science. Therefore, easy and fast access to reliable, long-term, and high-quality observational environmental data is recognised as fundamental to research and the development of environmental forecasting and assessment services. In our opinion article, we discuss the potential role that environmental research infrastructures in Europe (ENVRI RIs) can play in the context of an integrated global observation system. In particular, we focus on the role of the atmosphere-centred research infrastructures ACTRIS (Aerosol, Clouds and Trace Gases Research Infrastructure), IAGOS (In-service Aircraft for a Global Observing System), and ICOS (Integrated Carbon Observation System), also referred to as ATMO-RIs, with their capabilities for standardised collection and provision of long-term and high-quality observational data, complemented by rich metadata. The ATMO-RIs provide data through open access and offer data interoperability across different research fields including all fields of environmental sciences and beyond. As a result of these capabilities in data collection and provision, we elaborate on the novel research opportunities in atmospheric sciences which arise from the combination of open-access and interoperable observational data, tools, and technologies offered by data-intensive science and the emerging collaboration platform ENVRI-Hub, hosted by the European Open Science Cloud (EOSC).

2024

Detection flying aircraft from Landsat 8 OLI data

Zhao, F.; Xia, L.; Kylling, Arve; Li, R. Q.; Shang, H.; Xu, Ming

2018

Social-environmental analysis of methane in the South China Sea and bordering countries

Tseng, Hsiao-Chun; Newton, Alice; Chen, Chen-Tung Arthur; Borges, Alberto V.; DelValls, T. Angel

2018

New brominated flame retardants and dechlorane plus in the Arctic: Local sources and bioaccumulation potential in marine benthos

Carlsson, Pernilla; Vrana, Branislav; Sobotka, Jaromír; Borgå, Katrine; Bohlin-Nizzetto, Pernilla; Varpe, Øystein

The aim of the present study was to investigate the presence and bioaccumulation of new flame retardants (nBFRs), polybrominated diphenyl ethers (PBDEs) and dechlorane plus (DDC-CO) in the marine environment close to an Arctic community. Passive sampling of air and water and grab sampling of sediment and amphipods was used to obtain samples to study long-range transport versus local contributions for regulated and emerging flame retardants in Longyearbyen, Svalbard. BDE-47 and -99, α- and β-tetrabromoethylcyclohexane (DBE-DBCH), syn- and anti-dechlorane plus (DDC-CO) were detected in all investigated matrices and the DDC-COss at higher concentrations in the air than reported from other remote Arctic areas. Water concentrations of ΣDDC-COSs were low (3 pg/L) and comparable to recent Arctic studies. ΣnBFR was 37 pg/L in the water samples while ΣPBDE was 3 pg/L. In biota, ΣDDC-COSs dominated (218 pg/g ww) followed by ΣnBFR (95 pg/g ww) and ΣPBDEs (45 pg/g ww). When compared with other areas and their relative distribution patterns, contributions from local sources of the analysed compounds cannot be ruled out. This should be taken into account when assessing long-range transport of nBFRs and DDC-COs to the Arctic. High concentrations of PBDEs in the sediment indicate that they might originate from a small, local source, while the results for some of the more volatile compounds such as hexabromobenzene (HBBz) suggest long-range transport to be more important than local sources. We recommend that local sources of flame retardants in remote areas receive more attention in the future.

2018

The Eulerian urban dispersion model EPISODE – Part 2: Extensions to the source dispersion and photochemistry for EPISODE–CityChem v1.2 and its application to the city of Hamburg

Karl, Matthias; Walker, Sam-Erik; Solberg, Sverre; Ramacher, Martin O. P.

This paper describes the CityChem extension of the Eulerian urban dispersion model EPISODE. The development of the CityChem extension was driven by the need to apply the model in largely populated urban areas with highly complex pollution sources of particulate matter and various gaseous pollutants. The CityChem extension offers a more advanced treatment of the photochemistry in urban areas and entails specific developments within the sub-grid components for a more accurate representation of dispersion in proximity to urban emission sources. Photochemistry on the Eulerian grid is computed using a numerical chemistry solver. Photochemistry in the sub-grid components is solved with a compact reaction scheme, replacing the photo-stationary-state assumption. The simplified street canyon model (SSCM) is used in the line source sub-grid model to calculate pollutant dispersion in street canyons. The WMPP (WORM Meteorological Pre-Processor) is used in the point source sub-grid model to calculate the wind speed at plume height. The EPISODE–CityChem model integrates the CityChem extension in EPISODE, with the capability of simulating the photochemistry and dispersion of multiple reactive pollutants within urban areas. The main focus of the model is the simulation of the complex atmospheric chemistry involved in the photochemical production of ozone in urban areas. The ability of EPISODE–CityChem to reproduce the temporal variation of major regulated pollutants at air quality monitoring stations in Hamburg, Germany, was compared to that of the standard EPISODE model and the TAPM (The Air Pollution Model) air quality model using identical meteorological fields and emissions. EPISODE–CityChem performs better than EPISODE and TAPM for the prediction of hourly NO2 concentrations at the traffic stations, which is attributable to the street canyon model. Observed levels of annual mean ozone at the five urban background stations in Hamburg are captured by the model within ±15 %. A performance analysis with the FAIRMODE DELTA tool for air quality in Hamburg showed that EPISODE–CityChem fulfils the model performance objectives for NO2 (hourly), O3 (daily max. of the 8 h running mean) and PM10 (daily mean) set forth in the Air Quality Directive, qualifying the model for use in policy applications. Envisaged applications of the EPISODE–CityChem model are urban air quality studies, emission control scenarios in relation to traffic restrictions and the source attribution of sector-specific emissions to observed levels of air pollutants at urban monitoring stations.

2019

Socioeconomic position, lifestyle habits and biomarkers of epigenetic aging: A multi-cohort analysis

Fiorito, Giovanni; McCrory, Cathal; Robinson, Oliver; Carmeli, Cristian; Rosales, Carolina Ochoa; Zhang, Yan; Colicino, Elena; Dugué, Pierre-Antoine; Artaud, Fanny; McKay, Gareth J.; Jeong, Ayoung; Mishra, Pashupati P.; Nøst, Therese Haugdahl; Krogh, Vittorio; Panico, Salvatore; Sacerdote, Carlotta; Tumino, Rosario; Palli, Domenico; Matullo, Giuseppe; Guarrera, Simonetta; Gandini, Martina; Bochud, Murielle; Dermitzakis, Emmanouil; Muka, Taulant; Schwartz, Joel; Vokonas, Pantel S.; Just, Allan; Hodge, Allison M.; Giles, Graham G.; Southey, Melissa C.; Hurme, Mikko A.; Young, Ian; McKnight, Amy Jayne; Kunze, Sonja; Waldenberger, Melanie; Peters, Annette; Schwettmann, Lars; Lund, Eiliv; Baccarelli, Andrea; Milne, Roger L.; Kenny, Rose A.; Elbaz, Alexis; Brenner, Hermann; Kee, Frank; Voortman, Trudy; Probst-Hensch, Nicole; Lehtimäki, Terho; Elliot, Paul; Stringhini, Silvia; Vineis, Paolo; Polidoro, Silvia

Differences in health status by socioeconomic position (SEP) tend to be more evident at older ages, suggesting the involvement of a biological mechanism responsive to the accumulation of deleterious exposures across the lifespan. DNA methylation (DNAm) has been proposed as a biomarker of biological aging that conserves memory of endogenous and exogenous stress during life.

We examined the association of education level, as an indicator of SEP, and lifestyle-related variables with four biomarkers of age-dependent DNAm dysregulation: the total number of stochastic epigenetic mutations (SEMs) and three epigenetic clocks (Horvath, Hannum and Levine), in 18 cohorts spanning 12 countries.

The four biological aging biomarkers were associated with education and different sets of risk factors independently, and the magnitude of the effects differed depending on the biomarker and the predictor. On average, the effect of low education on epigenetic aging was comparable with those of other lifestyle-related risk factors (obesity, alcohol intake), with the exception of smoking, which had a significantly stronger effect.

Our study shows that low education is an independent predictor of accelerated biological (epigenetic) aging and that epigenetic clocks appear to be good candidates for disentangling the biological pathways underlying social inequalities in healthy aging and longevity.

2019

The Emissions Fractions Approach to Assessing the Long-Range Transport Potential of Organic Chemicals

Breivik, Knut; McLachlan, Michael S.; Wania, Frank

The assessment of long-range transport potential (LRTP) is enshrined in several frameworks for chemical regulation such as the Stockholm Convention. Screening for LRTP is commonly done with the OECD Pov and LRTP Screening Tool employing two metrics, characteristic travel distance (CTD) and transfer efficiency (TE). Here we introduce a set of three alternative metrics and implement them in the Tool’s model. Each metric is expressed as a fraction of the emissions in a source region. The three metrics quantify the extent to which the chemical (i) reaches a remote region (dispersion, ϕ1), (ii) is transferred to surface media in the remote region (transfer, ϕ2), and (iii) accumulates in these surface media (accumulation, ϕ3). In contrast to CTD and TE, the emissions fractions metrics can integrate transport via water and air, enabling comprehensive LRTP assessment. Furthermore, since there is a coherent relationship between the three metrics, the new approach provides quantitative mechanistic insight into different phenomena determining LRTP. Finally, the accumulation metric, ϕ3, allows assessment of LRTP in the context of the Stockholm Convention, where the ability of a chemical to elicit adverse effects in surface media is decisive. We conclude that the emission fractions approach has the potential to reduce the risk of false positives/negatives in LRTP assessments.

2022

EURODELTA III exercise: An evaluation of air quality models' capacity to reproduce the carbonaceous aerosol

Mircea, Mihaela; Bessagnet, Bertrand; D'Isidoro, Massimo; Pirovano, Guido; Aksoyoglu, Sebnem; Ciarelli, Giancarlo; Tsyro, Svetlana; Manders, Astrid; Bieser, Johannes; Stern, Rainer; Vivanco, Marta García; Cuvelier, Cornelius; Aas, Wenche; Prévôt, André S.H.; Aulinger, Armin; Briganti, Gino; Calori, Giuseppe; Cappelletti, Andrea; Colette, Augustin; Couvidat, Florian; Fagerli, Hilde; Finardi, Sandro; Kranenburg, Richard; Rouil, Laurence; Silibello, Camillo; Spindler, Gerald; Poulain, Laurent; Herrmann, Hartmut; Jimenez, Jose L.; Day, Douglas A.; Tiitta, Petri; Carbone, Samara

The carbonaceous aerosol accounts for an important part of total aerosol mass, affects human health and climate through its effects on physical and chemical properties of the aerosol, yet the understanding of its atmospheric sources and sinks is still incomplete. This study shows the state-of-the-art in modelling carbonaceous aerosol over Europe by comparing simulations performed with seven chemical transport models (CTMs) currently in air quality assessments in Europe: CAMx, CHIMERE, CMAQ, EMEP/MSC-W, LOTOS-EUROS, MINNI and RCGC. The simulations were carried out in the framework of the EURODELTA III modelling exercise and were evaluated against field measurements from intensive campaigns of European Monitoring and Evaluation Programme (EMEP) and the European Integrated Project on Aerosol Cloud Climate and Air Quality Interactions (EUCAARI). Model simulations were performed over the same domain, using as much as possible the same input data and covering four seasons: summer (1–30 June 2006), winter (8 January – 4 February 2007), autumn (17 September- 15 October 2008) and spring (25 February - 26 March 2009). The analyses of models’ performances in prediction of elemental carbon (EC) for the four seasons and organic aerosol components (OA) for the last two seasons show that all models generally underestimate the measured concentrations. The maximum underestimation of EC is about 60% and up to about 80% for total organic matter (TOM). The underestimation of TOM outside of highly polluted area is a consequence of an underestimation of secondary organic aerosol (SOA), in particular of its main contributor: biogenic secondary aerosol (BSOA). This result is independent on the SOA modelling approach used and season. The concentrations and daily cycles of total primary organic matter (TPOM) are generally better reproduced by the models since they used the same anthropogenic emissions. However, the combination of emissions and model formulation leads to overestimate TPOM concentrations in 2009 for most of the models. All models capture relatively well the SOA daily cycles at rural stations mainly due to the spatial resolution used in the simulations. For the investigated carbonaceous aerosol compounds, the differences between the concentrations simulated by different models are lower than the differences between the concentrations simulated with a model for different seasons.

2019

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

Aalmo, Giovanna Ottaviani; 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.

2022

Aerosol, Clouds and Trace Gases Research Infrastructure (ACTRIS): The European Research Infrastructure Supporting Atmospheric Science

Laj, Paolo; Myhre, Cathrine Lund; Riffault, Véronique; Amiridis, Vassilis; Fuchs, Hendrik; Eleftheriadis, Konstantinos; Petäjä, Tuukka; Salameh, Therese; Kivekäs, Niku; Juurola, Eija; Saponaro, Giulia; Philippin, Sabine; Cornacchia, Carmela; Arboledas, Lucas Alados; Baars, Holger; Claude, Anja; Mazière, Martine De; Dils, Bart; Dufresne, Marvin; Evangeliou, Nikolaos; Favez, Olivier; Fiebig, Markus; Haeffelin, Martial; Herrmann, Hartmut; Höhler, Kristina; Illmann, Niklas; Kreuter, Axel; Ludewig, Elke; Marinou, Eleni; Möhler, Ottmar; Mona, Lucia; Murberg, Lise Eder; Nicolae, Doina; Novelli, Anna; O'Connor, Ewan; Ohneiser, Kevin; Altieri, Rosa Maria Petracca; Picquet-Varrault, Benedicte; Pinxteren, Dominik van; Pospichal, Bernhard; Putaud, Jean-Philippe; Reimann, Stefan; Siomos, Nikolaos; Stachlewska, Iwona S.; Tillmann, Ralf; Voudouri, Kalliopi Artemis; Wandinger, Ulla; Wiedensohler, Alfred; Apituley, Arnoud; Comerón, Adolfo; Gysel-Beer, Martin; Mihalopoulos, Nikolaos; Nikolova, Nina; Pietruczuk, Aleksander; Sauvage, Stéphane; Sciare, Jean; Skov, Henrik; Svendby, Tove Marit; Swietlicki, Erik; Tonev, Dimitar; Vaughan, Geraint; Zdimal, Vladimir; Baltensperger, Urs; Doussin, Jean-François; Kulmala, Markku; Pappalardo, Gelsomina; Sundet, Sanna Sorvari; Vana, Milan

The Aerosol, Clouds and Trace Gases Research Infrastructure (ACTRIS) officially became the 33rd European Research Infrastructure Consortium (ERIC) on April 25, 2023 with the support of 17 founding member and observer countries. As a pan-European legal organization, ACTRIS ERIC will coordinate the provision of data and data products on short-lived atmospheric constituents and clouds relevant to climate and air pollution over the next 15-20 years. ACTRIS was designed more than a decade ago, and its development was funded at national and European levels. It was included in the European Strategy Forum on Research Infrastructures (ESFRI) Roadmap in 2016 and subsequently, in the national infrastructure roadmaps of European countries. It became a landmark of the ESFRI roadmap in 2021. The purpose of this paper is to describe the mission of ACTRIS, its added value to the community of atmospheric scientists, providing services to academia as well as the public and private sectors, and to summarize its main achievements. The present publication serves as a reference document for ACTRIS, its users and the scientific community as a whole. It provides the reader with relevant information and an overview on ACTRIS governance and services, as well as a summary of the main scientific achievements of the last 20 years. The paper concludes with an outlook on the upcoming challenges for ACTRIS and the strategy for its future evolution.

2024

Tackling Data Quality When Using Low-Cost Air Quality Sensors in Citizen Science Projects

Watne, Ågot K.; Linden, Jenny; Willhelmsson, Jens; Fridén, Håkan; Gustafsson, Malin; Castell, Nuria

Using low-cost air quality sensors (LCS) in citizen science projects opens many possibilities. LCS can provide an opportunity for the citizens to collect and contribute with their own air quality data. However, low data quality is often an issue when using LCS and with it a risk of unrealistic expectations of a higher degree of empowerment than what is possible. If the data quality and intended use of the data is not harmonized, conclusions may be drawn on the wrong basis and data can be rendered unusable. Ensuring high data quality is demanding in terms of labor and resources. The expertise, sensor performance assessment, post-processing, as well as the general workload required will depend strongly on the purpose and intended use of the air quality data. It is therefore a balancing act to ensure that the data quality is high enough for the specific purpose, while minimizing the validation effort. The aim of this perspective paper is to increase awareness of data quality issues and provide strategies to minimizing labor intensity and expenses while maintaining adequate QA/QC for robust applications of LCS in citizen science projects. We believe that air quality measurements performed by citizens can be better utilized with increased awareness about data quality and measurement requirements, in combination with improved metadata collection. Well-documented metadata can not only increase the value and usefulness for the actors collecting the data, but it also the foundation for assessment of potential integration of the data collected by citizens in a broader perspective.

2021

The dynamics of concentration fluctuations within passive scalar plumes in a turbulent neutral boundary layer

Cassiani, Massimo; Ardeshiri, Hamidreza; Pisso, Ignacio; Salizzoni, Pietro; Marro, Massimo; Stohl, Andreas; Stebel, Kerstin; Park, Soon-Young

We investigate the concentration fluctuations of passive scalar plumes emitted from small, localised (point-like) steady sources in a neutrally stratified turbulent boundary layer over a rough wall. The study utilises high-resolution large-eddy simulations for sources of varying sizes and heights. The numerical results, which show good agreement with wind-tunnel studies, are used to estimate statistical indicators of the concentration field, including spectra and moments up to the fourth order. These allow us to elucidate the mechanisms responsible for the production, transport and dissipation of concentration fluctuations, with a focus on the very near field, where the skewness is found to have negative values – an aspect not previously highlighted. The gamma probability density function is confirmed to be a robust model for the one-point concentration at sufficiently large distances from the source. However, for ground-level releases in a well-defined area around the plume centreline, the Gaussian distribution is found to be a better statistical model. As recently demonstrated by laboratory results, for elevated releases, the peak and shape of the pre-multiplied scalar spectra are confirmed to be independent of the crosswind location for a given downwind distance. Using a stochastic model and theoretical arguments, we demonstrate that this is due to the concentration spectra being directly shaped by the transverse and vertical velocity components governing the meandering of the plume. Finally, we investigate the intermittency factor, i.e. the probability of non-zero concentration, and analyse its variability depending on the thresholds adopted for its definition.

2024

Impact of 2020 COVID-19 lockdowns on particulate air pollution across Europe

Putaud, Jean-Philippe; Pisoni, Enrico; Mangold, Alexander; Hueglin, Christoph; Sciare, Jean; Pikridas, Michael; Savvides, Chrysantos; Ondráček, Jakub; Mbengue, Saliou; Wiedensohler, Alfred; Weinhold, Kay; Merkel, Maik; Poulain, Laurent; Pinxteren, Dominik van; Herrmann, Hartmut; Massling, Andreas; Nordstroem, Claus; Alastuey, Andres; Reche, Cristina; Perez, Noemi; Castillo, Sonia; Sorribas, Mar; Adame, Jose A.; Petäjä, Tuukka; Lehtipalo, Katrianne; Niemi, Jarkko; Riffault, Véronique; Brito, Joel F. De; Colette, Augustin; Favez, Olivier; Petit, Jean-Eudes; Gros, Valérie; Gini, Maria; Vratolis, Stergios; Eleftheriadis, Konstantinos; Diapouli, Evangelia; Gon, Hugo Denier van der; Yttri, Karl Espen; Aas, Wenche

To fight against the first wave of coronavirus disease 2019 (COVID-19) in 2020, lockdown measures were implemented in most European countries. These lockdowns had well-documented effects on human mobility. We assessed the impact of the lockdown implementation and relaxation on air pollution by comparing daily particulate matter (PM), nitrogen dioxide (NO2) and ozone (O3) concentrations, as well as particle number size distributions (PNSDs) and particle light absorption coefficient in situ measurement data, with values that would have been expected if no COVID-19 epidemic had occurred at 28 sites across Europe for the period 17 February–31 May 2020. Expected PM, NO2 and O3 concentrations were calculated from the 2020 Copernicus Atmosphere Monitoring Service (CAMS) ensemble forecasts, combined with 2019 CAMS ensemble forecasts and measurement data. On average, lockdown implementations did not lead to a decrease in PM2.5 mass concentrations at urban sites, while relaxations resulted in a +26 ± 21 % rebound. The impacts of lockdown implementation and relaxation on NO2 concentrations were more consistent (−29 ± 17 and +31 ± 30 %, respectively). The implementation of the lockdown measures also induced statistically significant increases in O3 concentrations at half of all sites (+13 % on average). An enhanced oxidising capacity of the atmosphere could have boosted the production of secondary aerosol at those places. By comparison with 2017–2019 measurement data, a significant change in the relative contributions of wood and fossil fuel burning to the concentration of black carbon during the lockdown was detected at 7 out of 14 sites. The contribution of particles smaller than 70 nm to the total number of particles significantly also changed at most of the urban sites, with a mean decrease of −7 ± 5 % coinciding with the lockdown implementation. Our study shows that the response of PM2.5 and PM10 mass concentrations to lockdown measures was not systematic at various sites across Europe for multiple reasons, the relationship between road traffic intensity and particulate air pollution being more complex than expected.

2023

Strengthened linkage between midlatitudes and Arctic in boreal winter

Xu, Xinping; He, Shengping; Gao, Yongqi; Furevik, Tore; Wang, Huijun; Li, Fei; Ogawa, Fumiaki

2019

MercuNorth–monitoring mercury in pregnant women from the Arctic as a baseline to assess the effectiveness of the Minamata Convention

Adlard, Bryan; Lemire, Mélanie; Bonefeld-Jørgensen, Eva Cecilie; Long, Manhai; Ólafsdóttir, Kristín; Odland, Jon Øyvind; Rautio, Arja; Myllynen, Päivi; Sandanger, Torkjel M; Dudarev, Alexey A.; Bergdahl, Ingvar A.; Wennberg, Maria; Berner, James; Ayotte, Pierre

Exposure to mercury (Hg) is a global concern, particularly among Arctic populations that rely on the consumption of marine mammals and fish which are the main route of Hg exposure for Arctic populations.The MercuNorth project was created to establish baseline Hg levels across several Arctic regions during the period preceding the Minamata Convention. Blood samples were collected from 669 pregnant women, aged 18–44 years, between 2010 and 2016 from sites across the circumpolar Arctic including Alaska (USA), Nunavik (Canada), Greenland, Iceland, Norway, Sweden, Northern Lapland (Finland) and Murmansk Oblast (Russia). Descriptive statistics were calculated, multiple pairwise comparisons were made between regions, and unadjusted linear trend analyses were performed.Geometric mean concentrations of total Hg were highest in Nunavik (5.20 µg/L) and Greenland (3.79 µg/L), followed by Alaska (2.13 µg/L), with much lower concentrations observed in the other regions (ranged between 0.48 and 1.29 µg/L). In Nunavik, Alaska and Greenland, blood Hg concentrations have decreased significantly since 1992, 2000 and 2010 respectively with % annual decreases of 4.7%, 7.5% and 2.7%, respectively.These circumpolar data combined with fish and marine mammal consumption data can be use

2021

Painted Wood Climate Risk Analysis by the HERIe Model of Building Protection and Conservation Heating Scenarios in Norwegian Medieval Stone Churches

Grøntoft, Terje; Stoveland, Lena Porsmo

HERIe was used to model the effect of changes to indoor climate on the risk of humidity-induced mechanical damage (cracking and plastic deformation) to wooden panels painted with stiff gesso in two Norwegian medieval stone churches: Kinn (mean relative humidity (RH, %) = 79%) on the humid west coast, and Ringsaker (mean RH = 49%) in the drier eastern part of the country. The risk involved in moving cultural heritage objects (paint on wood) between the churches and a conservation studio with more “ideal”, stable conditions was also modeled. A hypothetical reduction in RH to ~65% and, proportionally, of the climate fluctuations in Kinn, and an increase in the RH in Ringsaker to a more stable value of ~63% via conservation heating, were found to improve (Kinn) and uphold (Ringsaker) the conformity to relevant standards and significantly reduce the risk of damage, except in the scenario of moving objects from Ringsaker to a conservation studio, when the risk would increase. The use of conservation heating could save ~50% of the heating cost. The estimated risk reductions may be less relevant for objects kept in situ, where cracks in the original paint and gesso have developed historically. They may be more relevant when moving original objects away from their proofed climate into a conservation studio for treatment.

2023

Modelling the coupled mercury-halogen-ozone cycle in the central Arctic during spring

Ahmed, Shaddy; Thomas, Jennie L.; Angot, Hélène; Dommergue, Aurélien; Archer, Stephen D.; Bariteau, Ludovic; Beck, Ivo; Benavent, Nuria; Blechschmidt, Anne-Marlene; Blomquist, Byron; Boyer, Matthew; Christensen, Jesper H.; Dahlke, Sandro; Dastoor, Ashu; Helmig, Detlev; Howard, Dean; Jacobi, Hans-Werner; Jokinen, Tuija; Lapere, Rémy; Laurila, Tiia; Quéléver, Lauriane L.J.; Richter, Andreas; Ryjkov, Andrei; Mahajan, Anoop S.; Marelle, Louis; Pfaffhuber, Katrine Aspmo; Posman, Kevin; Rinke, Annette; Saiz-Lopez, Alfonso; Schmale, Julia; Skov, Henrik; Steffen, Alexandra; Stupple, Geoff; Stutz, Jochen; Travnikov, Oleg; Zilker, Bianca

Near-surface mercury and ozone depletion events occur in the lowest part of the atmosphere during Arctic spring. Mercury depletion is the first step in a process that transforms long-lived elemental mercury to more reactive forms within the Arctic that are deposited to the cryosphere, ocean, and other surfaces, which can ultimately get integrated into the Arctic food web. Depletion of both mercury and ozone occur due to the presence of reactive halogen radicals that are released from snow, ice, and aerosols. In this work, we added a detailed description of the Arctic atmospheric mercury cycle to our recently published version of the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem 4.3.3) that includes Arctic bromine and chlorine chemistry and activation/recycling on snow and aerosols. The major advantage of our modelling approach is the online calculation of bromine concentrations and emission/recycling that is required to simulate the hourly and daily variability of Arctic mercury depletion. We used this model to study coupling between reactive cycling of mercury, ozone, and bromine during the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) spring season in 2020 and evaluated results compared to land-based, ship-based, and remote sensing observations. The model predicts that elemental mercury oxidation is driven largely by bromine chemistry and that particulate mercury is the major form of oxidized mercury. The model predicts that the majority (74%) of oxidized mercury deposited to land-based snow is re-emitted to the atmosphere as gaseous elemental mercury, while a minor fraction (4%) of oxidized mercury that is deposited to sea ice is re-emitted during spring. Our work demonstrates that hourly differences in bromine/ozone chemistry in the atmosphere must be considered to capture the springtime Arctic mercury cycle, including its integration into the cryosphere and ocean.

2023

Plastic litter in the European Arctic: What do we know?

Halsband, Claudia; Herzke, Dorte

Despite an exponential increase in available data on marine plastic debris globally, information on levels and trends of plastic pollution and especially microplastics in the Arctic remains scarce. The few available peer-reviewed scientific works, however, point to a ubiquitous distribution of plastic particles in all environmental compartments, including sea ice. Here, we review the current state of knowledge on the sources, distribution, transport pathways and fate of meso- and microplastics with a focus on the European Arctic and discuss observed and projected impacts on biota and ecosystems.

2019

Surface-Bioengineered Extracellular Vesicles Seeking Molecular Biotargets in Lung Cancer Cells

Kowalczyk, Agata; Dziubak, Damian; Kasprzak, Artur; Sobczak, Kamil; Ruzycka-Ayoush, Monika; Bamburowicz-Klimkows, Magdalena; Sęk, Sławomir; Mondragon, Ivan Rios; Żołek, Teresa; Rundén-Pran, Elise; Shaposhnikov, Sergey; Cimpan, Mihaela Roxana; Dusinska, Maria; Grudzinski, Ireneusz P.; Nowicka, Anna M.

Personalized medicine is a new approach to modern oncology. Here, to facilitate the application of extracellular vesicles (EVs) derived from lung cancer cells as potent advanced therapy medicinal products in lung cancer, the EV membrane was functionalized with a specific ligand for targeting purposes. In this role, the most effective heptapeptide in binding to lung cancer cells (PTHTRWA) was used. The functionalization process of EV surface was performed through the C- or N-terminal end of the heptapeptide. To prove the activity of the EVs functionalized with PTHTRWA, both a model of lipid membrane mimicking normal and cancerous cell membranes as well as human adenocarcinomic alveolar basal epithelial cells (A549) and human normal bronchial epithelial cells (BEAS-2B) have been exposed to these bioconstructs. Magnetic resonance imaging (MRI) showed that the as-bioengineered PTHTRWA-EVs loaded with superparamagnetic iron oxide nanoparticle (SPIO) cargos reach the growing tumor when dosed intravenously in NUDE Balb/c mice bearing A549 cancer. Molecular dynamics (MD) in silico studies elucidated a high affinity of the synthesized peptide to the α5β1 integrin. Preclinical safety assays did not evidence any cytotoxic or genotoxic effects of the PTHTRWA-bioengineered EVs.

2024

Consistent histories of anthropogenic western European air pollution preserved in different Alpine ice cores

Eichler, Anja; Legrand, Michel; Jenk, Theo M.; Preunkert, Susanne; Andersson, Camilla; Eckhardt, Sabine; Engardt, Magnuz; Plach, Andreas; Schwikowski, Margit

Individual high-Alpine ice cores have been proven to contain a well-preserved history of past anthropogenic air pollution in western Europe. The question of how representative one ice core is with respect to the reconstruction of atmospheric composition in the source region has not been addressed so far. Here, we present the first study systematically comparing longer-term ice-core records (1750–2015 CE) of various anthropogenic compounds, such as major inorganic aerosol constituents (, , ), black carbon (BC), and trace species (Cd, F−, Pb). Depending on the data availability for the different air pollutants, up to five ice cores from four high-Alpine sites located in the European Alps analysed by different laboratories were considered. Whereas absolute concentration levels can partly differ depending on the prevailing seasonal distribution of accumulated precipitation, all seven investigated anthropogenic compounds are in excellent agreement between the various sites for their respective, species-dependent longer-term concentration trends. This is related to common source regions of air pollution impacting the four sites less than 100 km away including western European countries surrounding the Alps. For individual compounds, the Alpine ice-core composites developed in this study allowed us to precisely time the onset of pollution caused by industrialization in western Europe. Extensive emissions from coal combustion and agriculture lead to an exceeding of pre-industrial (1750–1850) concentration levels already at the end of the 19th century for BC, Pb, (non-dust, non-sea salt ), and , respectively. However, Cd, F−, and concentrations started surpassing pre-industrial values only in the 20th century, predominantly due to pollution from zinc and aluminium smelters and traffic. The observed maxima of BC, Cd, F−, Pb, and concentrations in the 20th century and a significant decline afterwards clearly reveal the efficiency of air pollution control measures such as the desulfurization of coal, the introduction of filters and scrubbers in power plants and metal smelters, and the ban of leaded gasoline improving the air quality in western Europe. In contrast, and concentration records show levels in the beginning of the 21th century which are unprecedented in the context of the past 250 years, indicating that the introduced abatement measures to reduce these pollutants were insufficient to have a major effect at high altitudes in western Europe. Only four ice-core composite records (BC, F−, Pb, ) of the seven investigated pollutants correspond well with modelled trends, suggesting inaccuracies of the emission estimates or an incomplete representation of chemical reaction mechanisms in the models for the other pollutants. Our results demonstrate that individual ice-core records from different sites in the European Alps generally provide a spatially representative signal of anthropogenic air pollution trends in western European countries.

2023

Estimating methane emissions in the Arctic nations using surface observations from 2008 to 2019

Wittig, Sophie; Berchet, Antoine; Pison, Isabelle; Saunois, Marielle; Thanwerdas, Joel; Martinez, Adrien; Paris, Jean-Daniel; Machida, Toshinobu; Sasakawa, Motoki; Worthy, Doug E.J.; Lan, Xin; Thompson, Rona Louise; Sollum, Espen; Arshinov, Mikhail

The Arctic is a critical region in terms of global warming. Environmental changes are already progressing steadily in high northern latitudes, whereby, among other effects, a high potential for enhanced methane (CH4) emissions is induced. With CH4 being a potent greenhouse gas, additional emissions from Arctic regions may intensify global warming in the future through positive feedback. Various natural and anthropogenic sources are currently contributing to the Arctic's CH4 budget; however, the quantification of those emissions remains challenging. Assessing the amount of CH4 emissions in the Arctic and their contribution to the global budget still remains challenging. On the one hand, this is due to the difficulties in carrying out accurate measurements in such remote areas. Besides, large variations in the spatial distribution of methane sources and a poor understanding of the effects of ongoing changes in carbon decomposition, vegetation and hydrology also complicate the assessment. Therefore, the aim of this work is to reduce uncertainties in current bottom-up estimates of CH4 emissions as well as soil oxidation by implementing an inverse modelling approach in order to better quantify CH4 sources and sinks for the most recent years (2008 to 2019). More precisely, the objective is to detect occurring trends in the CH4 emissions and potential changes in seasonal emission patterns. The implementation of the inversion included footprint simulations obtained with the atmospheric transport model FLEXPART (FLEXible PARTicle dispersion model), various emission estimates from inventories and land surface models, and data on atmospheric CH4 concentrations from 41 surface observation sites in the Arctic nations. The results of the inversion showed that the majority of the CH4 sources currently present in high northern latitudes are poorly constrained by the existing observation network. Therefore, conclusions on trends and changes in the seasonal cycle could not be obtained for the corresponding CH4 sectors. Only CH4 fluxes from wetlands are adequately constrained, predominantly in North America. Within the period under study, wetland emissions show a slight negative trend in North America and a slight positive trend in East Eurasia. Overall, the estimated CH4 emissions are lower compared to the bottom-up estimates but higher than similar results from global inversions.

2023

Mercury isotope evidence for Arctic summertime re-emission of mercury from the cryosphere

Araujo, Beatriz Ferreira; Osterwalder, Stefan; Szponar, Natalie; Lee, Domenica; Petrova, Mariia V.; Pernov, Jakob Boyd; Ahmed, Shaddy; Heimbürger-Boavida, Lars-Eric; Laffont, Laure; Teisserenc, Roman; Tananaev, Nikita; Nordstrom, Claus; Magand, Olivier; Stupple, Geoff; Skov, Henrik; Steffen, Alexandra; Bergquist, Bridget; Pfaffhuber, Katrine Aspmo; Thomas, Jennie L.; Scheper, Simon; Petäjä, Tuukka; Dommergue, Aurélien; Sonke, Jeroen E.

During Arctic springtime, halogen radicals oxidize atmospheric elemental mercury (Hg0), which deposits to the cryosphere. This is followed by a summertime atmospheric Hg0 peak that is thought to result mostly from terrestrial Hg inputs to the Arctic Ocean, followed by photoreduction and emission to air. The large terrestrial Hg contribution to the Arctic Ocean and global atmosphere has raised concern over the potential release of permafrost Hg, via rivers and coastal erosion, with Arctic warming. Here we investigate Hg isotope variability of Arctic atmospheric, marine, and terrestrial Hg. We observe highly characteristic Hg isotope signatures during the summertime peak that reflect re-emission of Hg deposited to the cryosphere during spring. Air mass back trajectories support a cryospheric Hg emission source but no major terrestrial source. This implies that terrestrial Hg inputs to the Arctic Ocean remain in the marine ecosystem, without substantial loss to the global atmosphere, but with possible effects on food webs.

2022

Tropospheric ozone assessment report: Global ozone metrics for climate change, human health, and crop/ecosystem research

Lefohn, Allen S.; Malley, Christopher S.; Smith, Luther; Wells, Benjamin; Hazucha, Milan; Simon, Heather; Naik, Vaishali; Mills, Gina; Schultz, Martin G.; Paoletti, Elena; Marco, Alessandra De; Xu, Xiaobin; Zhang, Li; Wang, Tao; Neufeld, Howard S.; Musselman, Robert C.; Tarasick, David; Brauer, Michael; Feng, Zhaozhong; Tang, Haoye; Kobayashi, Kazuhiko; Sicard, Pierre; Solberg, Sverre; Gerosa, Giacomo

Assessment of spatial and temporal variation in the impacts of ozone on human health, vegetation, and climate requires appropriate metrics. A key component of the Tropospheric Ozone Assessment Report (TOAR) is the consistent calculation of these metrics at thousands of monitoring sites globally. Investigating temporal trends in these metrics required that the same statistical methods be applied across these ozone monitoring sites. The nonparametric Mann-Kendall test (for significant trends) and the Theil-Sen estimator (for estimating the magnitude of trend) were selected to provide robust methods across all sites. This paper provides the scientific underpinnings necessary to better understand the implications of and rationale for selecting a specific TOAR metric for assessing spatial and temporal variation in ozone for a particular impact. The rationale and underlying research evidence that influence the derivation of specific metrics are given. The form of 25 metrics (4 for model-measurement comparison, 5 for characterization of ozone in the free troposphere, 11 for human health impacts, and 5 for vegetation impacts) are described. Finally, this study categorizes health and vegetation exposure metrics based on the extent to which they are determined only by the highest hourly ozone levels, or by a wider range of values. The magnitude of the metrics is influenced by both the distribution of hourly average ozone concentrations at a site location, and the extent to which a particular metric is determined by relatively low, moderate, and high hourly ozone levels. Hence, for the same ozone time series, changes in the distribution of ozone concentrations can result in different changes in the magnitude and direction of trends for different metrics. Thus, dissimilar conclusions about the effect of changes in the drivers of ozone variability (e.g., precursor emissions) on health and vegetation exposure can result from the selection of different metrics.

2018

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