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Pollutant concentrations are poorly known for the largest animals on Earth, blue whales Balaenoptera musculus and fin whales Balaenoptera physalus. In this study, concentrations of persistent organic pollutants (POPs) were determined in blubber biopsies and stable isotope values for nitrogen (δ15N) and carbon (δ13C) were measured using skin biopsies for 18 blue whales and 12 fin whales sampled in waters surrounding the Svalbard Archipelago, Norway. The samples were collected in summer during the period 2014–2018. POPs were dominated by DDTs, PCBs and toxaphenes, with median concentrations in blue/fin whales being 208/341, 127/275 and 133/233 ng/g lipid weight, respectively. Linear models indicated that pollutant concentrations were 1.6–3 times higher in fin whales than in blue whales, which is likely related to the higher trophic positions of fin whales, as indicated by their higher δ15N. Lower δ13C in fin whales suggests that they feed at higher latitudes than blue whales; these values were not correlated with pollutant concentrations. Pollutant levels were approximately twice as high in males compared to females (intraspecifically), which indicates that females of these species offload pollutants to their offspring during gestation and lactation, similar to many other mammalian species. Pollutant concentrations in balaenopterid whales from Svalbard waters were generally much lower than in conspecific whales from the Mediterranean Sea or the Gulf of California, but higher than those in conspecifics from the Antarctic Peninsula.
2020
Biomass burning related aerosol episodes are becoming a serious threat to the radiative balance of the Arctic region. Since early July 2017 intense wildfires were recorded between August and September in Canada and Greenland, covering an area up to 4674 km2 in size. This paper describes the impact of these biomass burning (BB) events measured over Svalbard, using an ensemble of ground-based, columnar, and vertically-resolved techniques. BB influenced the aerosol chemistry via nitrates and oxalates, which exhibited an increase in their concentrations in all of size fractions, indicating the BB origin of particles. The absorption coefficient data (530 nm) at ground reached values up to 0.6 Mm–1, highlighting the impact of these BB events when compared to average Arctic background values, which do not exceed 0.05 Mm–1. The absorption behavior is fundamental as implies a subsequent atmospheric heating. At the same time, the AERONET Aerosol Optical Depth (AOD) data showed high values at stations located close to or in Canada (AOD over 2.0). Similarly, increased values of AODs were then observed in Svalbard, e.g., in Hornsund (daily average AODs exceeded 0.14 and reached hourly values up to 0.5). Elevated values of AODs were then registered in Sodankylä and Andenes (daily average AODs exceeding 0.150) a few days after the Svalbard observation of the event highlighting the BB columnar magnitude, which is crucial for the radiative impact. All the reported data suggest to rank the summer 2017 plume of aerosols as one of the biggest atmosphere related environmental problems over Svalbard region in last 10 years
2020
Organic contaminants (polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), and chlorinated paraffins (CPs)) and heavy metals and metalloids (Ag, Cd, Co, Cr, Cu, Hg, Ni, Pb, Sb, Zn) were analysed in surface soil samples from the Agbogbloshie e-waste processing and dumping site in Accra (Ghana). In order to identify which of the pollutants are likely to be linked specifically to handling of e-waste, samples were also collected from the Kingtom general waste site in Freetown (Sierra Leone). The results were compared using principal component analyses (PCA). PBDE congeners found in technical octa-BDE mixtures, highly chlorinated PCBs and several heavy metals (Cu, Pb, Ni, Cd, Ag and Hg) showed elevated concentrations in the soils that are likely due to contamination by e-waste. PCAs associated those compounds with pyrogenic PAHs, suggesting that burning of e-waste, a common practice to isolate valuable metals, may cause this contamination. Moreover, other contamination pathways, especially incorporation of waste fragments into the soil, also appeared to play an important role in determining concentrations of some of the pollutants in the soil. Concentrations of several of these compounds were extremely high (especially PBDEs, heavy metals and SCCPs) and in some cases exceeded action guideline levels for soil. This indicates that exposure to these contaminants via the soil alone is potentially harmful to the recyclers and their families living on waste sites. Many organic contaminants and other exposure pathways such as inhalation are not yet included in such guidelines but may also be significant, given that deposition from the air following waste burning was identified as a major pollutant source.
2020
We employ JRA-55 (Japanese 55-year Reanalysis), a recent second-generation global reanalysis providing data of high quality in the stratosphere, to examine whether a distinguishable effect of geomagnetic activity on Northern Hemisphere stratospheric temperatures can be detected. We focus on how the statistical significance of stratospheric temperature differences may be robustly assessed during years with high and low geomagnetic activity. Two problems must be overcome. The first is the temporal autocorrelation of the data, which is addressed with a correction of the t statistics by means of the estimate of the number of independent values in the series of correlated values. The second is the problem of multiplicity due to strong spatial autocorrelations, which is addressed by means of a false discovery rate (FDR) procedure. We find that the statistical tests fail to formally reject the null hypothesis, i.e. no significant response to geomagnetic activity can be found in the seasonal-mean Northern Hemisphere stratospheric temperature record.
2020
Evaluating the effectiveness of a stove exchange programme on PM 2.5 emission reduction
Residential wood combustion (RWC) is one of the most important sources of particulate matter () in urban areas. As a consequence, different types of regulatory instruments are being implemented to reduce emissions. In this study, we evaluate both the potential and actual effect of a subsidy programme for stove exchange, which has been in place for over 20 years in Oslo (Norway). The subsidy programme provides economic support to the inhabitants for substituting old stoves for RWC with new and cleaner stoves as a measure to reduce emissions. Different approaches were selected to assess the potential effect of the Oslo subsidy programme. First, we evaluate the potential for reductions in emissions and pollution levels through the use of emission and dispersion modelling under different scenarios. We then assess the actual reductions associated with the stoves already replaced with the subsidy. We conclude the study by evaluating the time variation (2005 to 2018) in emissions, wood consumption and emission factors in Oslo in comparison with other municipalities with and without subsidy programmes in place. Results from emission and dispersion modelling show that the replacement of old wood stoves for new ones could have a significant effect on the reduction of emissions (up to 46%) and levels (up to 21%). Despite that, with near 8% of the total existing stoves in Oslo being exchanged with subsidy, the potential for reduction based on improved emission factors was estimated to be smaller by an order of magnitude. We find no evidence that municipalities with subsidy reduce emissions faster than those without subsidy. We therefore conclude that there is no evidence from our modelling results, supported by available observation data, that indicate that the emissions or concentrations in Oslo have been reduced as a result of the subsidy programme.
2020
2020
The influence of residential wood combustion on the concentrations of PM2.5 in four Nordic cities
Residential wood combustion (RWC) is an important contributor to air quality in numerous regions worldwide. This study is the first extensive evaluation of the influence of RWC on ambient air quality in several Nordic cities. We have analysed the emissions and concentrations of PM2.5 in cities within four Nordic countries: in the metropolitan areas of Copenhagen, Oslo, and Helsinki and in the city of Umeå. We have evaluated the emissions for the relevant urban source categories and modelled atmospheric dispersion on regional and urban scales. The emission inventories for RWC were based on local surveys, the amount of wood combusted, combustion technologies and other relevant factors. The accuracy of the predicted concentrations was evaluated based on urban concentration measurements. The predicted annual average concentrations ranged spatially from 4 to 7 µg m−3 (2011), from 6 to 10 µg m−3 (2013), from 4 to more than 13 µg m−3 (2013) and from 9 to more than 13 µg m−3 (2014), in Umeå, Helsinki, Oslo and Copenhagen, respectively. The higher concentrations in Copenhagen were mainly caused by the relatively high regionally and continentally transported background contributions. The annual average fractions of PM2.5 concentrations attributed to RWC within the considered urban regions ranged spatially from 0 % to 15 %, from 0 % to 20 %, from 8 % to 22 % and from 0 % to 60 % in Helsinki, Copenhagen, Umeå and Oslo, respectively. In particular, the contributions of RWC in central Oslo were larger than 40 % as annual averages. In Oslo, wood combustion was used mainly for the heating of larger blocks of flats. In contrast, in Helsinki, RWC was solely used in smaller detached houses. In Copenhagen and Helsinki, the highest fractions occurred outside the city centre in the suburban areas. In Umeå, the highest fractions occurred both in the city centre and its surroundings.
2020
A comprehensive quantification of global nitrous oxide sources and sinks
Nitrous oxide (N2O), like carbon dioxide, is a long-lived greenhouse gas that accumulates in the atmosphere. Over the past 150 years, increasing atmospheric N2O concentrations have contributed to stratospheric ozone depletion1 and climate change2, with the current rate of increase estimated at 2 per cent per decade. Existing national inventories do not provide a full picture of N2O emissions, owing to their omission of natural sources and limitations in methodology for attributing anthropogenic sources. Here we present a global N2O inventory that incorporates both natural and anthropogenic sources and accounts for the interaction between nitrogen additions and the biochemical processes that control N2O emissions. We use bottom-up (inventory, statistical extrapolation of flux measurements, process-based land and ocean modelling) and top-down (atmospheric inversion) approaches to provide a comprehensive quantification of global N2O sources and sinks resulting from 21 natural and human sectors between 1980 and 2016. Global N2O emissions were 17.0 (minimum–maximum estimates: 12.2–23.5) teragrams of nitrogen per year (bottom-up) and 16.9 (15.9–17.7) teragrams of nitrogen per year (top-down) between 2007 and 2016. Global human-induced emissions, which are dominated by nitrogen additions to croplands, increased by 30% over the past four decades to 7.3 (4.2–11.4) teragrams of nitrogen per year. This increase was mainly responsible for the growth in the atmospheric burden. Our findings point to growing N2O emissions in emerging economies—particularly Brazil, China and India. Analysis of process-based model estimates reveals an emerging N2O–climate feedback resulting from interactions between nitrogen additions and climate change. The recent growth in N2O emissions exceeds some of the highest projected emission scenarios3,4, underscoring the urgency to mitigate N2O emissions.
2020
This paper describes the Eulerian urban dispersion model EPISODE. EPISODE was developed to address a need for an urban air quality model in support of policy, planning, and air quality management in the Nordic, specifically Norwegian, setting. It can be used for the calculation of a variety of airborne pollutant concentrations, but we focus here on the implementation and application of the model for NO2 pollution. EPISODE consists of an Eulerian 3D grid model with embedded sub-grid dispersion models (e.g. a Gaussian plume model) for dispersion of pollution from line (i.e. roads) and point sources (e.g. chimney stacks). It considers the atmospheric processes advection, diffusion, and an NO2 photochemistry represented using the photostationary steady-state approximation for NO2. EPISODE calculates hourly air concentrations representative of the grids and at receptor points. The latter allow EPISODE to estimate concentrations representative of the levels experienced by the population and to estimate their exposure. This methodological framework makes it suitable for simulating NO2 concentrations at fine-scale resolution (<100 m) in Nordic environments. The model can be run in an offline nested mode using output concentrations from a global or regional chemical transport model and forced by meteorology from an external numerical weather prediction model; it also can be driven by meteorological observations. We give a full description of the overall model function and its individual components. We then present a case study for six Norwegian cities whereby we simulate NO2 pollution for the entire year of 2015. The model is evaluated against in situ observations for the entire year and for specific episodes of enhanced pollution during winter. We evaluate the model performance using the FAIRMODE DELTA Tool that utilises traditional statistical metrics, e.g. root mean square error (RMSE), Pearson correlation R, and bias, along with some specialised tests for air quality model evaluation. We find that EPISODE attains the DELTA Tool model quality objective in all of the stations we evaluate against. Further, the other statistical evaluations show adequate model performance but that the model scores greatly improved correlations during winter and autumn compared to the summer. We attribute this to the use of the photostationary steady-state scheme for NO2, which should perform best in the absence of local ozone photochemical production. Oslo does not comply with the NO2 annual limit set in the 2008/50/EC directive (AQD). NO2 pollution episodes with the highest NO2 concentrations, which lead to the occurrence of exceedances of the AQD hourly limit for NO2, occur primarily in the winter and autumn in Oslo, so this strongly supports the use of EPISODE for application to these wintertime events. Overall, we conclude that the model is suitable for an assessment of annual mean NO2 concentrations and also for the study of hourly NO2 concentrations in the Nordic winter and autumn environment. Further, in this work we conclude that it is suitable for a range of policy applications specific to NO2 that include pollution episode analysis, evaluation of seasonal statistics, policy and planning support, and air quality management. Lastly, we identify a series of model developments specifically designed to address the limitations of the current model assumptions. Part 2 of this two-part paper discusses the CityChem extension to EPISODE, which includes a number of implementations such as a more comprehensive photochemical scheme suitable for describing more chemical species and a more diverse range of photochemical environments, as well as a more advanced treatment of the sub-grid dispersion.
2020
Public Perception of Urban Air Quality Using Volunteered Geographic Information Services
Investigating perceived air quality (AQ) in urban areas is a rather new topic of interest. Papers presenting results from studies on perception of AQ have thus far focused on the individual characteristics leading to a certain AQ perception or have compared personal perception with on-site measurements. Here we present a novel approach, namely applying volunteered geographic information (VGI) technologies in urban AQ monitoring. We present two smartphone applications that have been developed and applied in two EU projects (FP7 CITI-SENSE and H2020 hackAIR) to obtain citizens’ perception of AQ. We focus on observations reported through the smartphone apps for the greater Oslo area in Norway. In order to evaluate whether the reports on perceived AQ contain information about the actual spatial patterns of AQ, we carried out a comparison of the perception data against the output from the high-resolution urban AQ model EPISODE. The results indicate an association between modelled annual average pollutant concentrations and the provided perception reports. This demonstrates that the spatial patterns of perceived AQ are not entirely random but follow to some extent what would be expected due to proximity of emission sources and transport. This information shows that VGI about citizens’ perception of AQ has the potential to identify areas with low environmental quality for urban development.
2020
Atmospheric transport is a major pathway of microplastics to remote regions
In recent years, marine, freshwater and terrestrial pollution with microplastics has been discussed extensively, whereas atmospheric microplastic transport has been largely overlooked. Here, we present global simulations of atmospheric transport of microplastic particles produced by road traffic (TWPs – tire wear particles and BWPs – brake wear particles), a major source that can be quantified relatively well. We find a high transport efficiencies of these particles to remote regions. About 34% of the emitted coarse TWPs and 30% of the emitted coarse BWPs (100 kt yr−1 and 40 kt yr−1 respectively) were deposited in the World Ocean. These amounts are of similar magnitude as the total estimated direct and riverine transport of TWPs and fibres to the ocean (64 kt yr−1). We suggest that the Arctic may be a particularly sensitive receptor region, where the light-absorbing properties of TWPs and BWPs may also cause accelerated warming and melting of the cryosphere.
2020
The Arctic is one of the most rapidly warming regions of the Earth, with predicted temperature increases of 5–7 ∘C and the accompanying extensive retreat of Arctic glacial systems by 2100. Retreating glaciers will reveal new land surfaces for microbial colonisation, ultimately succeeding to tundra over decades to centuries. An unexplored dimension to these changes is the impact upon the emission and consumption of halogenated organic compounds (halocarbons). Halocarbons are involved in several important atmospheric processes, including ozone destruction, and despite considerable research, uncertainties remain in the natural cycles of some of these compounds. Using flux chambers, we measured halocarbon fluxes across the glacier forefield (the area between the present-day position of a glacier's ice-front and that at the last glacial maximum) of a high-Arctic glacier in Svalbard, spanning recently exposed sediments (<10 years) to approximately 1950-year-old tundra. Forefield land surfaces were found to consume methyl chloride (CH3Cl) and methyl bromide (CH3Br), with both consumption and emission of methyl iodide (CH3I) observed. Bromoform (CHBr3) and dibromomethane (CH2Br2) have rarely been measured from terrestrial sources but were here found to be emitted across the forefield. Novel measurements conducted on terrestrial cyanobacterial mats covering relatively young surfaces showed similar measured fluxes to the oldest, vegetated tundra sites for CH3Cl, CH3Br, and CH3I (which were consumed) and for CHCl3 and CHBr3 (which were emitted). Consumption rates of CH3Cl and CH3Br and emission rates of CHCl3 from tundra and cyanobacterial mat sites were within the ranges reported from older and more established Arctic tundra elsewhere. Rough calculations showed total emissions and consumptions of these gases across the Arctic were small relative to other sources and sinks due to the small surface area represented by glacier forefields. We have demonstrated that glacier forefields can consume and emit halocarbons despite their young age and low soil development, particularly when cyanobacterial mats are present.
2020
Atmospheric concentration of legacy (LFRs) and emerging flame retardants (EFRs) including 8 polybrominated diphenyl ethers (PBDEs), 6 novel brominated flame retardants (NBFRs), 2 dechlorane plus isomers (DP), and 8 chlorinated organophosphate flame retardants (OPFRs) were consecutively measured in eight major cities across Pakistan. A total of 96 samples (48 PM2.5 & 48 PUFs) were analyzed and the concentrations of ∑8PBDEs (gaseous+particulate) ranged between 40.8 and 288 pg/m3 with an average value of 172 pg/m3. ∑6NBFRs ranged between 12.0 and 35.0 pg/m3 with an average value of 22.5 pg/m3 while ∑8OPFRs ranged between 12,900–40,800 pg/m3 with an average of 24,700 pg/m3. Among the studied sites, Faisalabad city exhibited the higher concentrations of FRs among all cities which might be a consequence of textile mills and garment manufacturing industries. While analyzing the diurnal patterns, OPFRs depicted higher concentrations during night-time. The estimated risks of all groups of FRs from inhalation of ambient air were negligible for all the cities, according to USEPA guidelines. Nonetheless, our study is the first to report gaseous and particulate concentrations of FRs in air on a diurnal basis across major cities in Pakistan, offering insights into the atmospheric fate of these substances in urban areas in a sub-tropical region.
2020
2020
Car Tire Crumb Rubber: Does Leaching Produce a Toxic Chemical Cocktail in Coastal Marine Systems?
Crumb rubber granulate (CRG) produced from end of life tires (ELTs) is commonly applied to synthetic turf pitches (STPs), playgrounds, safety surfaces and walkways. In addition to fillers, stabilizers, cross-linking agents and secondary components (e.g., pigments, oils, resins), ELTs contain a range of other organic compound and heavy metal additives. While previous environmental impact studies on CRG have focused on terrestrial soil and freshwater ecosystems, many sites applying CRG in Norway are coastal. The current study investigated the organic chemical and metal additive content of ‘pristine’ and ‘weathered’ CRG and their seawater leachates, as well as uptake and effects of leachate exposure using marine copepods (Acartia and Calanus sp.). A combination of pyrolysis gas chromatography mass spectrometry (py-GC-MS) and chemical extraction followed by GC-MS analysis revealed similar organic chemical profiles for pristine and weathered CRG, including additives such as benzothiazole, N-1,3-dimethylbutyl-N′-phenyl-p-phenylenediamine and a range of polycyclic aromatic hydrocarbons (PAHs) and phenolic compounds (e.g., bisphenols). ICP-MS analysis revealed g kg–1 quantities of Zn and mg kg–1 quantities of Fe, Mn, Cu, Co, Cr, Pb, and Ni in the CRG. A cocktail of organic additives and metals readily leached from the CRG into seawater, with the most abundant leachate components being benzothiazole and Zn, Fe, Co (metals), as well as detectable levels of PAHs and phenolic compounds. Concentrations of individual components varied with CRG source material and CRG to seawater ratio, but benzothiazole and Zn were typically the organic and metal components present at the highest concentrations in the leachates. While organic chemical concentrations in the leachates stabilized within days, metals continued to leach out over the 30-day period. Marine copepods exposed to high CRG leachate concentrations exhibited high mortalities within 48 h. The smaller lipid-poor Acartia had a higher sensitivity to leachates than the larger lipid-rich Calanus, indicating species-specific differences in vulnerability to leachates. The effect on survival was alleviated at lower leachate concentrations, indicating a dose-response relationship. Benzothiazole and its derivatives appear to be of concern owing to their proven toxicity, while bisphenols are also known to be toxic and were enriched in the leachates relative to the other compounds in the CRG.
2020
Satellite validation strategy assessments based on the AROMAT campaigns
The Airborne ROmanian Measurements of Aerosols and Trace gases (AROMAT) campaigns took place in Romania in September 2014 and August 2015. They focused on two sites: the Bucharest urban area and large power plants in the Jiu Valley. The main objectives of the campaigns were to test recently developed airborne observation systems dedicated to air quality studies and to verify their applicability for the validation of space-borne atmospheric missions such as the TROPOspheric Monitoring Instrument (TROPOMI)/Sentinel-5 Precursor (S5P). We present the AROMAT campaigns from the perspective of findings related to the validation of tropospheric NO2, SO2, and H2CO. We also quantify the emissions of NOx and SO2 at both measurement sites.
We show that tropospheric NO2 vertical column density (VCD) measurements using airborne mapping instruments are well suited for satellite validation in principle. The signal-to-noise ratio of the airborne NO2 measurements is an order of magnitude higher than its space-borne counterpart when the airborne measurements are averaged at the TROPOMI pixel scale. However, we show that the temporal variation of the NO2 VCDs during a flight might be a significant source of comparison error. Considering the random error of the TROPOMI tropospheric NO2 VCD (σ), the dynamic range of the NO2 VCDs field extends from detection limit up to 37 σ (2.6×1016 molec. cm−2) and 29 σ (2×1016 molec. cm−2) for Bucharest and the Jiu Valley, respectively. For both areas, we simulate validation exercises applied to the TROPOMI tropospheric NO2 product. These simulations indicate that a comparison error budget closely matching the TROPOMI optimal target accuracy of 25 % can be obtained by adding NO2 and aerosol profile information to the airborne mapping observations, which constrains the investigated accuracy to within 28 %. In addition to NO2, our study also addresses the measurements of SO2 emissions from power plants in the Jiu Valley and an urban hotspot of H2CO in the centre of Bucharest. For these two species, we conclude that the best validation strategy would consist of deploying ground-based measurement systems at well-identified locations.
2020
Seabirds like gulls are common indicators in contaminant monitoring. The herring gull (Larus argentatus) is a generalist with a broad range of dietary sources, possibly introducing a weakness in its representativeness of aquatic contamination. To investigate the herring gull as an indicator of contamination in an urban‐influenced fjord, the Norwegian Oslofjord, we compared concentrations of a range of lipophilic and protein‐associated organohalogen contaminants (OHCs), Hg, and dietary markers in blood (n = 15), and eggs (n = 15) between the herring gull and the strict marine‐feeding common eider (Somateria mollissima) in the breeding period of May 2017. Dietary markers showed that the herring gull was less representative of the marine food web than the common eider. We found higher concentrations of lipophilic OHCs (wet weight and lipid weight) and Hg (dry weight) in the blood of common eider (mean ± SE ∑PCB = 210 ± 126 ng/g ww, 60 600 ± 28 300 ng/g lw; mean Hg = 4.94 ± 0.438 ng/g dw) than of the herring gull (mean ± SE ∑PCB = 19.0 ± 15.6 ng/g ww, 1210 ± 1510 ng/g lw; mean Hg = 4.26 ± 0.438 ng/g dw). Eggs gave opposite results; higher wet weight and lipid weight OHC concentrations in the herring gull (mean ± SE ∑PCB = 257 ± 203 ng/g ww, 3240 ± 2610 ng/g lw) than the common eider (mean ± SE ∑PCB = 18.2 ± 20.8 ng/g ww, 101 ± 121 ng/g lw), resulting in higher OHC maternal transfer ratios in gulls than eiders. We suggest that the matrix differences are due to fasting during incubation in the common eider. We suggest that in urban areas, herring gull might not be representative as an indicator of marine contamination but rather urban contaminant exposure. The common eider is a better indicator of marine pollution in the Oslofjord. The results are influenced by the matrix choice, as breeding strategy affects lipid dynamics regarding the transfer of lipids and contaminants to eggs and remobilization of contaminants from lipids to blood during incubation, when blood is drawn from the mother. Our results illustrate the benefit of a multispecies approach for a thorough picture of contaminant status in urban marine ecosystems. Integr Environ Assess Manag 2020;00:1–12. © 2020 The Authors. Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC)
2020
Polycyclic aromatic hydrocarbons (PAHs) are not declining in Arctic air despite reductions in their global emissions. In Svalbard, the Longyearbyen coal-fired power plant is considered to be one of the major local sources of PAHs. Power plant stack emissions and ambient air samples, collected simultaneously at 1 km (UNIS) and 6 km (Adventdalen) transect distance, were analysed (gaseous and particulate phases separately) for 22 nitro-PAHs, 8 oxy-PAHs, and 16 parent PAHs by gas chromatography in combination with single quadrupole electron capture negative ionization mass spectrometry (GC-ECNI-MS) and gas chromatography in combination with triple quadrupole electron ionization mass spectrometry (GC-EI-MS/MS). Results confirm low levels of PAH emissions (Sum 16 PAHs D 1:5 μg/kg coal) from the power plant. Phenanthrene, 9,10-anthraquinone, 9- fluorenone, fluorene, fluoranthene, and pyrene accounted for 85% of the plant emission (not including naphthalene). A dilution effect was observed for the transect ambient air samples: 1.26+/- 0.16 and 0.63+/- 0.14 ng/m3 were the sum of all 47 PAH derivatives for UNIS and Adventdalen, respectively. The PAH profile was homogeneous for these recipient stations with phenanthrene and 9-fluorenone being most abundant. Multivariate statistical analysis confirmed coal combustion and vehicle and marine traffic as the predominant sources of PAHs. Secondary atmospheric formation of 9- nitroanthracene and 2C3-nitrofluoranthene was evaluated and concluded. PAHs partitioning between gaseous and particulate phases showed a strong dependence on ambient temperatures and humidity. The present study contributes important data which can be utilized to eliminate uncertainties in model predictions that aim to assess the extent and impacts of Arctic atmospheric contaminants.
2020
Atmospheric turbulence and in particular its effect on tracer dispersion may be measured by cameras sensitive to the absorption of ultraviolet (UV) sunlight by sulfur dioxide (SO2), a gas that can be considered a passive tracer over short transport distances. We present a method to simulate UV camera measurements of SO2 with a 3D Monte Carlo radiative transfer model which takes input from a large eddy simulation (LES) of a SO2 plume released from a point source. From the simulated images the apparent absorbance and various plume density statistics (centre-line position, meandering, absolute and relative dispersion, and skewness) were calculated. These were compared with corresponding quantities obtained directly from the LES. Mean differences of centre-line position, absolute and relative dispersions, and skewness between the simulated images and the LES were generally found to be smaller than or about the voxel resolution of the LES. Furthermore, sensitivity studies were made to quantify how changes in solar azimuth and zenith angles, aerosol loading (background and in plume), and surface albedo impact the UV camera image plume statistics. Changing the values of these parameters within realistic limits has negligible effects on the centre-line position, meandering, absolute and relative dispersions, and skewness of the SO2 plume. Thus, we demonstrate that UV camera images of SO2 plumes may be used to derive plume statistics of relevance for the study of atmospheric turbulent dispersion.
2020
Plants rely on spectral cues present in their surroundings, generated by the constantly changing light environment, to guide their growth and reproduction. Photoreceptors mediate the capture of information by plants from the light environment over a wide range of wavelengths, but despite extensive evidence that plants respond to various light cues, only fragmentary data have been published showing patterns of diurnal, seasonal and geographical variation in the spectral composition of daylight. To illustrate patterns in spectral photon ratios, we measured time series of irradiance spectra at two distinct geographical and climatological locations, Helsinki, Finland and Gual Pahari, India. We investigated the drivers behind variation of the spectral photon ratios measured at these two locations, based on the analysis of over 400 000 recorded spectra. Differences in spectral irradiance were explained by different atmospheric factors identified through multiple regression model analysis and comparison to spectral irradiance at ground level simulated with a radiative transfer model. Local seasonal and diurnal changes in spectral photon ratios were related to solar elevation angle, atmospheric water-vapour content and total ozone column thickness and deviated from their long-term averages to an extent likely to affect plant photobiology. We suggest that future studies should investigate possible effects of varying photon ratios on terrestrial plants. Solar elevation angle especially affects the patterns of B:G and B:R ratios. Water vapour has a large effect on the R:FR photon ratio and modelled climate scenarios predict that increasing global temperatures will result in increased atmospheric water vapour. The development of proxy models, utilising available data from weather and climate models, for relevant photon ratios as a function of solar elevation angle and atmospheric factors would facilitate the interpretation of results from past, present and future field studies of plants and vegetation.
2020
The white-tailed eagle (Haliaeetus albicilla) in Scandinavia has suffered from impaired reproduction due to high exposure to industrial pollution between the 1960s and 1980s. While population numbers are rising again, new contaminants, such as per- and polyfluoroalkyl substances (PFAS), are increasingly found in high trophic avifauna and are of concern to potentially impact once again on population health. In the present study, we examined PFAS levels in plasma of white-tailed eagle nestlings from northern Norway over the last decade (2008–2017). While PFOA and PFNA exposure did not follow a significant time trend, PFOS and PFHxS concentrations decreased over time, and ≥C11 perfluorinated carboxylic acids only seem to level off during the last four years. This may in fact be the first evidence for a change in the trend for some of these compounds. Furthermore, since several PFAS are expected to be highly present in aqueous film-forming foams used at airports, we also investigate the potential of the two main airports in the region to act as hotspots for PFAS. Our results indeed show decreasing exposure to PFOA with distance to the airports. Altogether, our results seem to show that legislation actions are effective, and continued concern for PFAS exposure of high trophic wildlife is still warranted, even in the northern environment.
2020
Grouping strategies are needed for per- and polyfluoroalkyl substances (PFAS), in part, because it would be time and resource intensive to test and evaluate the more than 4700 PFAS on the global market on a chemical-by-chemical basis. In this paper we review various grouping strategies that could be used to inform actions on these chemicals and outline the motivations, advantages and disadvantages for each. Grouping strategies are subdivided into (1) those based on the intrinsic properties of the PFAS (e.g. persistence, bioaccumulation potential, toxicity, mobility, molecular size) and (2) those that inform risk assessment through estimation of cumulative exposure and/or effects. The most precautionary grouping approach of those reviewed within this article suggests phasing out PFAS based on their high persistence alone (the so-called “P-sufficient” approach). The least precautionary grouping approach reviewed advocates only grouping PFAS for risk assessment that have the same toxicological effects, modes and mechanisms of action, and elimination kinetics, which would need to be well documented across different PFAS. It is recognised that, given jurisdictional differences in chemical assessment philosophies and methodologies, no one strategy will be generally acceptable. The guiding question we apply to the reviewed grouping strategies is: grouping for what purpose? The motivation behind the grouping (e.g. determining use in products vs. setting guideline levels for contaminated environments) may lead to different grouping decisions. This assessment provides the necessary context for grouping strategies such that they can be adopted as they are, or built on further, to protect human and environmental health from potential PFAS-related effects.
2020
Solar UV radiation measurements in Marambio, Antarctica, during years 2017–2019
In March 2017, measurements of downward global irradiance of ultraviolet (UV) radiation were started with a multichannel GUV-2511 radiometer in Marambio, Antarctica (64.23∘ S; 56.62∘ W), by the Finnish Meteorological Institute (FMI) in collaboration with the Servicio Meteorológico Nacional (SMN). These measurements were analysed and the results were compared to previous measurements performed at the same site with the radiometer of the Antarctic NILU-UV network during 2000–2008 and to data from five stations across Antarctica. In 2017/2018 the monthly-average erythemal daily doses from October to January were lower than those averaged over 2000–2008 with differences from 2.3 % to 25.5 %. In 2017/2018 the average daily erythemal dose from September to March was 1.88 kJ m−2, while in 2018/2019 it was 23 % larger (2.37 kJ m−2). Also at several other stations in Antarctica the UV radiation levels in 2017/2018 were below average. The maximum UV indices (UVI) in Marambio were 6.2 and 9.5 in 2017/2018 and 2018/2019, respectively, whereas during years 2000–2008 the maximum was 12. Cloud cover, the strength of the polar vortex and the stratospheric ozone depletion are the primary factors that influence the surface UV radiation levels in Marambio. The lower UV irradiance values in 2017/2018 are explained by the high ozone concentrations in November, February and for a large part of October. The role of cloud cover was clearly seen in December, and to a lesser extent in October and November, when cloud cover qualitatively explains changes which could not be ascribed to changes in total ozone column (TOC). In this study, the roles of aerosols and albedo are of minor influence because the variation of these factors in Marambio was small from one year to the other. The largest variations of UV irradiance occur during spring and early summer when noon solar zenith angle (SZA) is low and the stratospheric ozone concentration is at a minimum (the so-called ozone hole). In 2017/2018, coincident low total ozone column and low cloudiness near solar noon did not occur, and no extreme UV indices were measured.
2020
Arctic sea-ice loss intensifies aerosol transport to the Tibetan Plateau
The Tibetan Plateau (TP) has recently been polluted by anthropogenic emissions transported from South Asia, but the mechanisms conducive to this aerosol delivery are poorly understood. Here we show that winter loss of Arctic sea ice over the subpolar North Atlantic boosts aerosol transport toward the TP in April, when the aerosol loading is at its climatological maximum and preceding the Indian summer monsoon onset. Low sea ice in February weakens the polar jet, causing decreased Ural snowpack via reduced transport of warm, moist oceanic air into the high-latitude Eurasian interior. This diminished snowpack persists through April, reinforcing the Ural pressure ridge and East Asian trough, segments of a quasi-stationary Rossby wave train extending across Eurasia. These conditions facilitate an enhanced subtropical westerly jet at the southern edge of the TP, invigorating upslope winds that combine with mesoscale updrafts to waft emissions over the Himalayas onto the TP.
2020