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Black Carbon (BC) aerosol is a major climate forcer in the Arctic. Here, we present 15 years (2001–2015) of surface observations of the aerosol absorption coefficient babs (corresponding to Equivalent BC), obtained at the Zeppelin Observatory, Ny Ålesund, Svalbard, coupled with backward transport modeling with Flexpart in order to calculate the Potential Source Contribution Function (PSCF) for BC. The observed long‐term variability superimposed on a strong annual cycle is studied as a function of large‐scale circulation patterns represented by monthly index values for the North Atlantic Oscillation (NAO) and the Scandinavian pattern (SCAN). We find a 35% increase of babs values at Zeppelin during the SCAN− phase in the winter half‐year compared to the SCAN+ phase but no significant difference in babs values between the NAO index phases. Both NAO and SCAN induce significant regional variability on the areas of origin of babs, mainly Siberia, Europe, and North America. Plain Language Summary: Here, we investigate the effect of the most important large circulation patterns for the European Arctic, namely the North Atlantic Oscillation (NAO) and Scandinavian (SCAN) patterns on the light absorbing carbon aerosol reaching the highly important area experiencing the effects of climate change as found before. We report important first time findings for an extended observation record of 15 years of aerosol light absorbing carbon, which was never been employed before as a continuous long record, and we performed the first rigorous assessment of the impact of large atmospheric circulation patterns like NAO and SCAN on the transport of black carbon aerosol expressed as the climate relevant aerosol absorption coefficient (babs) for the first time. We find a significant 35% increase in babs at Zeppelin during one of the phases of the SCAN. However, a significant regional variability induced by both NAO and SCAN phases is revealed. These findings allow a better quantified estimate of the fate of emissions over the years in the Northern Hemisphere and a better assessment of their influence in the observed BC metrics in the Artic. Key Points: An extended 15 years' observation record of Arctic aerosol light absorbing carbon is employedLarge‐scale circulation patterns appear to induce a long‐term modulation in aerosol absorption coefficient (babs) with regional featuresA 35% increase is found in babs at Zeppelin during the negative Scandinavian pattern (SCAN) phase in the 6‐month cold period compared to the positive SCAN phase [ABSTRACT FROM AUTHOR]

Aerosols have important impacts on air quality and climate, but the processes affecting their removal from the atmosphere are not fully understood and are poorly constrained by observations. This makes modelled aerosol lifetimes uncertain. In this study, we make use of an observational constraint on aerosol lifetimes provided by radionuclide measurements and investigate the causes of differences within a set of global models. During the Fukushima Dai-Ichi nuclear power plant accident of March 2011, the radioactive isotopes cesium-137 (137Cs) and xenon-133 (133Xe) were released in large quantities. Cesium attached to particles in the ambient air, approximately according to their available aerosol surface area. 137Cs size distribution measurements taken close to the power plant suggested that accumulation-mode (AM) sulphate aerosols were the main carriers for the cesium. Hence, 137Cs can be used as a proxy tracer for the AM sulphate aerosol's fate in the atmosphere. In contrast, the noble gas 133Xe behaves almost like a passive transport tracer. Global surface measurements of the two radioactive isotopes taken over several months after the release allow the derivation of a lifetime of the carrier aerosol. We compare this to the lifetimes simulated by 19 different atmospheric transport models initialized with identical emissions of 137Cs that were assigned to an aerosol tracer with each model's default properties of AM sulphate, and 133Xe emissions that were assigned to a passive tracer. We investigate to what extent the modelled sulphate tracer can reproduce the measurements, especially with respect to the observed loss of aerosol mass with time. Modelled 37Cs and 133Xe concentrations sampled at the same location and times as station measurements allow a direct comparison between measured and modelled aerosol lifetime. The e-folding lifetime τe, calculated from station measurement data taken between two and nine weeks after the start of the emissions, is 14.3 days (95% confidence interval 13.1-15.7 days). The equivalent modelled τe lifetimes have a large spread, varying between 4.8 and 26.7 days with a model median of 9.4±2.3 days, indicating too fast removal in most models. Because sufficient measurement data were only available from about two weeks after the release, the estimated lifetimes apply to aerosols that have undergone long-range transport, i.e. not for freshly emitted aerosol. However, modelled instantaneous lifetimes show that the initial removal in the first two weeks was quicker (lifetimes between 1-5 days) due to the emissions occurring at low altitudes and co-location of the fresh plume with strong precipitation. Deviations between measured and modelled aerosol lifetimes are largest for the northernmost stations and at later time periods, suggesting that models do not transport enough of the aerosol towards the Arctic. The models underestimate passive tracer (133Xe) concentrations in the Arctic as well but to a smaller extent than for the aerosol (137Cs) tracer. This indicates that in addition to too fast aerosol removal in the models, errors in simulated atmospheric transport towards the Arctic in most models also contribute to the Arctic aerosol underestimates. [ABSTRACT FROM AUTHOR]

The coupled model LMDZORINCA has been used to simulate the transport, wet and dry deposition of the radioactive tracer 137Cs after accidental releases. For that reason, two horizontal resolutions were deployed and used in the model, a regular grid of 2.5° × 1.27°, and the same grid stretched over Europe to reach a resolution of 0.66° × 0.51°. The vertical dimension is represented with two different resolutions, 19 and 39 levels respectively, extending up to the mesopause. Four different simulations are presented in this work; the first uses the regular grid over 19 vertical levels assuming that the emissions took place at the surface (RG19L(S)), the second also uses the regular grid over 19 vertical levels but realistic source injection heights (RG19L); in the third resolution the grid is regular and the vertical resolution 39 levels (RG39L) and finally, it is extended to the stretched grid with 19 vertical levels (Z19L). The model is validated with the Chernobyl accident which occurred in Ukraine (ex-USSR) on 26 May 1986 using the emission inventory from Brandt et al. (2002). This accident has been widely studied since 1986, and a large database has been created containing measurements of atmospheric activity concentration and total cumulative deposition for 137Cs from most of the European countries. According to the results, the performance of the model to predict the transport and deposition of the radioactive tracer was efficient and accurate presenting low biases in activity concentrations and deposition inventories, despite the large uncertainties on the intensity of the source released. The best agreement with observations was obtained using the highest horizontal resolution of the model (Z19L run). The model managed to predict the radioactive contamination in most of the European regions (similar to De Cort et al., 1998), and also the arrival times of the radioactive fallout. As regards to the vertical resolution, the largest biases were obtained for the 39 layers run due to the increase of the levels in conjunction with the uncertainty of the source term. Moreover, the ecological half-life of 137Cs in the atmosphere after the accident ranged between 6 and 9 days, which is in good accordance to what previously reported and in the same range with the recent accident in Japan. The high response of LMDZORINCA model for 137Cs reinforces the importance of atmospheric modelling in emergency cases to gather information for protecting the population from the adverse effects of radiation. [ABSTRACT FROM AUTHOR]

The coupled model LMDzORINCA has been used to simulate the transport, wet and dry deposition of the radioactive tracer 137Cs after accidental releases. For that reason, two horizontal resolutions were deployed and used in the model, a regular grid of 2.5° x 1.25°, and the same grid stretched over Europe to reach a resolution of 0.45° x 0.51°. The vertical dimension is represented with two different resolutions, 19 and 39 levels, respectively, extending up to mesopause. Four different simulations are presented in this work; the first uses the regular grid over 19 vertical levels assuming that the emissions took place at the surface (RG19L(S)), the second also uses the regular grid over 19 vertical levels but realistic source injection heights (RG19L); in the third resolution the grid is regular and the vertical resolution 39 vertical levels (RG39L) and finally, it is extended to the stretched grid with 19 vertical levels (Z19L). The best choice for the model validation was the Chernobyl accident which occurred in Ukraine (ex-USSR) on 26 May 1986. This accident has been widely studied since 1986, and a large database has been created containing measurements of atmospheric activity concentration and total cumulative deposition for 137Cs from most of the European countries. According to the results, the performance of the model to predict the transport and deposition of the radioactive tracer was efficient and accurate presenting low biases in activity concentrations and deposition inventories, despite the large uncertainties on the intensity of the source released. However, the best agreement with observations was obtained using the highest horizontal resolution of the model (Z19L run). The model managed to predict the radioactive contamination in most of the European regions (similar to Atlas), and also the arrival times of the radioactive fallout. As regards to the vertical resolution, the largest biases were obtained for the 39 layers run due to the increase of the levels in conjunction with the uncertainty of the source term. Moreover, the ecological half-life of 137Cs in the atmosphere after the accident ranged between 6 and 9 days, which is in good accordance to what previously reported and in the same range with the recent accident in Japan. The high response of LMDzORINCA model for 137Cs reinforces the importance of atmospheric modeling in emergency cases to gather information for protecting the population from the adverse effects of radiation. [ABSTRACT FROM AUTHOR]

The vertical distribution of natural radionuclides (232Th decay, 238U decay, 40K and 210Pb) was assessed in sediment cores collected from the Amvrakikos Gulf, (Ionian Sea, Western Greece). Two collection stations were selected, the first at the western part of the Gulf near Preveza Strait (13A station) and the other near the centre of the Gulf (13B station). Activity concentrations were measured by means of gamma-ray spectrometry using high-purity germanium (HPGe) detectors installed at two national laboratories. The activity concentration of 226Ra was found in a range from 10 to 20 Bq kg−1, while the activity concentration of 222Rn daughters (214Pb, 214Bi) ranged from 6 to 20 Bq kg−1. The activity concentration of 228Ac varied from 20 to 28 Bq kg−1, while 220Rn daughters (212Pb, 208Tl) from 7 to 35 Bq kg−1. As concerns 40K and 210Pb, their activities varied from 400 to 830 Bq kg−1 and from 11 to 360 Bq kg−1, respectively. Also, the data of 210Pb were utilised in the calculations of the sedimentation rate along the sediment cores. Both locations were characterised by a consistent pattern with the average rates of 0.55 ± 0.02 and 0.32 ± 0.02 cm y−1, corresponding to 13A and 13B stations, respectively. Finally, the measurements constituted the basis of the first reported database concerning the radiological condition of the Gulf and which can be reclaimed as reference values in future monitoring studies. [ABSTRACT FROM AUTHOR]

Abstract: Caesium-137 activity concentration in the water columns of the Gulf of Patras (Central Greece) and the North-Eastern Aegean Sea (easterward to Lemnos Island) was investigated in selected sampling stations during the period September 2004–June 2006. The methodology followed was based on the sorption of caesium (Cs) on cotton wound cartridge filters impregnated by Cu2[Fe(CN)6] via in-situ pumping. In terms of the horizontal and vertical records, the activity concentrations of 137Cs in the Gulf of Patras ranged between 1.2 and 6.7Bqm−3, depending on the sampling period and the prevailing physicochemical regime at the sampling station. The general pattern of the decreased activity concentrations of 137Cs with increasing depth was reversed in the Gulf of Patras during the cold period attributed to the prevailing advective processes of the area. The activity concentrations of 137Cs in the North-Eastern Aegean Sea ranged from 2.6 to 12.8Bqm−3, whereas significant stratified curves were observed during the warm period and also, in one station during the cold period. In terms of temporal variation, the discharges in the Gulf of Patras resulted in enhanced levels of 137Cs, whereas in the North Aegean Sea the incoming water masses form the Black Sea had an apparent influence throughout the year by increasing the 137Cs levels, hence presenting a weak seasonal variation. Comparing the two studied areas, one could say that the North Aegean Sea, as an open sea environment, presented higher concentrations due to the influence of the Black Sea water masses. The estimated inventories of 137Cs in the Gulf of Patras ranged 0.25±0.03–0.79±0.03kBqm−2, whereas in the North-Eastern Aegean Sea they ranged 0.33±0.02–0.92±0.03kBqm−2. [Copyright &y& Elsevier]

The 1783-1784 Laki eruption provides a natural experiment to evaluate the performance of chemistry-transport models in predicting the health impact of air particulate pollution. There are few existing daily meteorological observations during the second part of the 18th century. Hence, creating reasonable climatological conditions for such events constitutes a major challenge. We reconstructed meteorological fields for the period 1783-1784 based on a technique of analogues described in the Methods. Using these fields and including detailed chemistry we describe the concentrations of sulphur (SO2/SO4) that prevail over the North Atlantic, the adjoining seas and Western Europe during these 2 years. To evaluate the model, we analyse these results through the prism of two datasets contemporary to the Laki period: • The date of the first appearance of ‘dry fogs’ over Europe, • The excess mortality recorded in French parishes over the period June-September 1783. The sequence of appearances of the dry fogs is reproduced with a very-high degree of agreement to the first dataset. High concentrations of SO2/SO4 are simulated in June 1783 that coincide with a rapid rise of the number of deceased in French parishes records. We show that only a small part of the deceased of the summer of 1783 can be explained by the present-day relationships between PM2.5 and relative risk. The implication of this result is that other external factors such as the particularly warm summer of 1783, and the lack of health care at the time, must have contributed to the sharp increase in mortality over France recorded from June to September 1783. [ABSTRACT FROM AUTHOR]

Abstract: The radiological status of the Greek marine environment, prior to the Chernobyl accident, was characterized mainly by the fallout from nuclear weapon tests. However, the release of radioactivity into the environment from the accident in the Chernobyl Nuclear Power Plant and its deposition in the Greek marine environment resulted in an increase of the 137Cs activity concentration by approximately one order of magnitude. In addition, the direct transport of radiocaesium into the North Aegean Sea has been further influenced by the late impact of the Chernobyl accident on the Greek marine environment, related to the transfer of 137Cs, mainly through the Dnieper but also the Danube rivers, to the Black Sea and further to the North Aegean Sea through the Straits of Dardanelles. The aim of this work is to provide a present day picture of the geographic variation of the concentration of 137Cs in the surface layer of the Greek marine environment and hence, to evaluate the annual committed effective dose delivered to humans through the ingestion pathway from marine sources. [Copyright &y& Elsevier]

The Fenwei Plain is one of China's most polluted regions, with poor atmospheric dispersion conditions and an outdated energy structure. After implementing multiple policies in recent years, significant reductions in air pollutant concentrations were observed. In this study, based on the Lagrangian-Bayesian inversion framework FLEXINVERT, we constructed a variable resolution inversion system focusing on the Fenwei Plain and inferred the carbon monoxide (CO) emissions using in-situ atmospheric CO observations from April 2014 to March 2020. We analyzed the spatiotemporal variations of the CO emissions and discussed their causes, especially the effect of the "Three-year Action Plan on Defending the Blue Sky" (TAPDBS). Before the policy, CO emissions temporarily increased, and the overall decrease in CO emissions per unit of Gross Domestic Product (GDP) slowed down. When the policy was implemented, CO emission fluxes declined sharply, with an average drop of 28%, accompanied by an even higher 37% decrease of CO emission per GDP. The reasons for the decline in CO emissions in Shanxi, Shaanxi and Henan are diverse. The decrease in energy intensity is the reason for CO emission reduction in Shannxi and Henan province but not in Shanxi province. This research fills the gap in emission information in recent years and confirms that TAPDBS has brought a breakthrough in both economic development and air quality protection in the Fenwei Plain., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Few studies report the occurrence of microplastics (MP), including tire wear particles (TWP) in the marine atmosphere, and little data is available regarding their size or sources. Here we present active air sampling devices (low- and high-volume samplers) for the evaluation of composition and MP mass loads in the marine atmosphere. Air was sampled during a research cruise along the Norwegian coast up to Bear Island. Samples were analyzed with pyrolysis-gas chromatography-mass spectrometry, generating a mass-based data set for MP in the marine atmosphere. Here we show the ubiquity of MP, even in remote Arctic areas with concentrations up to 37.5 ng m -3 . Cluster of polyethylene terephthalate (max. 1.5 ng m -3 ) were universally present. TWP (max. 35 ng m -3 ) and cluster of polystyrene, polypropylene, and polyurethane (max. 1.1 ng m -3 ) were also detected. Atmospheric transport and dispersion models, suggested the introduction of MP into the marine atmosphere equally from sea- and land-based emissions, transforming the ocean from a sink into a source for MP., (© 2023. The Author(s).)

Black carbon emitted by incomplete combustion of fossil fuels and biomass has a net warming effect in the atmosphere and reduces the albedo when deposited on ice and snow; accurate knowledge of past emissions is essential to quantify and model associated global climate forcing. Although bottom-up inventories provide historical Black Carbon emission estimates that are widely used in Earth System Models, they are poorly constrained by observations prior to the late 20th century. Here we use an objective inversion technique based on detailed atmospheric transport and deposition modeling to reconstruct 1850 to 2000 emissions from thirteen Northern Hemisphere ice-core records. We find substantial discrepancies between reconstructed Black Carbon emissions and existing bottom-up inventories which do not fully capture the complex spatial-temporal emission patterns. Our findings imply changes to existing historical Black Carbon radiative forcing estimates are necessary, with potential implications for observation-constrained climate sensitivity., (© 2023. The Author(s).)

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 (< 5 mm) are transported to the ocean, while riverine transport is between 3.3 and 14 Tg y -1 . We calculate that 0.418 ± 0.201 Tg y -1 MPs/MFs (size up to 250 and 2500 µm) were transported from the land to ocean (large particles were ignored). Model validation against observations showed that particle removal must be urgently updated in global models., (Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.)