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2019
Information on the origin of pollution constitutes an essential step of air quality management as it helps identifying measures to control air pollution. In this work, we review the most widely used source-apportionment methods for air quality management. Using theoretical and real-case datasets we study the differences among these methods and explain why they result in very different conclusions to support air quality planning. These differences are a consequence of the intrinsic assumptions that underpin the different methodologies and determine/limit their range of applicability. We show that ignoring their underlying assumptions is a risk for efficient/successful air quality management as these methods are sometimes used beyond their scope and range of applicability. The simplest approach based on increments (incremental approach) is often not suitable to support air quality planning. Contributions obtained through mass-transfer methods (receptor models or tagging approaches built in air quality models) are appropriate to support planning but only for specific pollutants. Impacts obtained via “brute-force” methods are the best suited but it is important to assess carefully their application range to make sure they reproduce correctly the prevailing chemical regimes.
Elsevier
2019
BioMed Central (BMC)
2019
2019
American Geophysical Union (AGU)
2019
2019
2019
Supporting the improvement of air quality management practices: The “FAIRMODE pilot” activity
Academic Press
2019
Monitoring Soil Moisture Drought over Northern High Latitudes from Space
Mapping drought from space using, e.g., surface soil moisture (SSM), has become viable in the last decade. However, state of the art SSM retrieval products suffer from very poor coverage over northern latitudes. In this study, we propose an innovative drought indicator with a wider spatial and temporal coverage than that obtained from satellite SSM retrievals. We evaluate passive microwave brightness temperature observations from the Soil Moisture and Ocean Salinity (SMOS) satellite as a surrogate drought metric, and introduce a Standardized Brightness Temperature Index (STBI). We compute the STBI by fitting a Gaussian distribution using monthly brightness temperature data from SMOS; the normal assumption is tested using the Shapior-Wilk test. Our results indicate that the assumption of normally distributed brightness temperature data is valid at the 0.05 significance level. The STBI is validated against drought indices from a land surface data assimilation system (LDAS-Monde), two satellite derived SSM indices, one from SMOS and one from the ESA CCI soil moisture project and a standardized precipitation index based on in situ data from the European Climate Assessment & Dataset (ECA&D) project. When comparing the temporal dynamics of the STBI to the LDAS-Monde drought index we find that it has equal correlation skill to that of the ESA CCI soil moisture product ( 0.71 ). However, in addition the STBI provides improved spatial coverage because no masking has been applied over regions with dense boreal forest. Finally, we evaluate the STBI in a case study of the 2018 Nordic drought. The STBI is found to provide improved spatial and temporal coverage when compared to the drought index created from satellite derived SSM over the Nordic region. Our results indicate that when compared to drought indices from precipitation data and a land data assimilation system, the STBI is qualitatively able to capture the 2018 drought onset, severity and spatial extent. We did see that the STBI was unable to detect the 2018 drought recovery for some areas in the Nordic countries. This false drought detection is likely linked to the recovery of vegetation after the drought, which causes an increase in the passive microwave brightness temperature, hence the STBI shows a dry anomaly instead of normal conditions, as seen for the other drought indices. We argue that the STBI could provide additional information for drought monitoring in regions where the SSM retrieval problem is not well defined. However, it then needs to be accompanied by a vegetation index to account for the recovery of the vegetation which could cause false drought detection.
MDPI
2019
Using meteor wind data from the Super Dual Auroral Radar Network (SuperDARN) in the Northern Hemisphere, we (1) demonstrate that the migrating (Sun‐synchronous) tides can be separated from the nonmigrating components in the mesosphere and lower thermosphere (MLT) region and (2) use this to determine the response of the different components of the semidiurnal tide (SDT) to sudden stratospheric warming (SSW) conditions. The radars span a limited range of latitudes around 60°N and are located over nearly 180° of longitude. The migrating tide is extracted from the nonmigrating components observed in the meridional wind recorded from meteor ablation drift velocities around 95‐km altitude, and a 20‐year climatology of the different components is presented. The well‐documented late summer and wintertime maxima in the semidiurnal winds are shown to be due primarily to the migrating SDT, whereas during late autumn and spring the nonmigrating components are at least as strong as the migrating SDT. The robust behavior of the SDT components during SSWs is then examined by compositing 13 SSW events associated with an elevated stratopause recorded between 1995 and 2013. The migrating SDT is seen to reduce in amplitude immediately after SSW onset and then return anomalously strongly around 10–17 days after the SSW onset. We conclude that changes in the underlying wind direction play a role in modulating the tidal amplitude during the evolution of SSWs and that the enhancement in the midlatitude migrating SDT (previously reported in modeling studies) is observed in the MLT at least up to 60°N.
American Geophysical Union (AGU)
2019
Recent Trends in Stratospheric Chlorine From Very Short-Lived Substances
Very short‐lived substances (VSLS), including dichloromethane (CH2Cl2), chloroform (CHCl3), perchloroethylene (C2Cl4), and 1,2‐dichloroethane (C2H4Cl2), are a stratospheric chlorine source and therefore contribute to ozone depletion. We quantify stratospheric chlorine trends from these VSLS (VSLCltot) using a chemical transport model and atmospheric measurements, including novel high‐altitude aircraft data from the NASA VIRGAS (2015) and POSIDON (2016) missions. We estimate VSLCltot increased from 69 (±14) parts per trillion (ppt) Cl in 2000 to 111 (±22) ppt Cl in 2017, with >80% delivered to the stratosphere through source gas injection, and the remainder from product gases. The modeled evolution of chlorine source gas injection agrees well with historical aircraft data, which corroborate reported surface CH2Cl2 increases since the mid‐2000s. The relative contribution of VSLS to total stratospheric chlorine increased from ~2% in 2000 to ~3.4% in 2017, reflecting both VSLS growth and decreases in long‐lived halocarbons. We derive a mean VSLCltot growth rate of 3.8 (±0.3) ppt Cl/year between 2004 and 2017, though year‐to‐year growth rates are variable and were small or negative in the period 2015–2017. Whether this is a transient effect, or longer‐term stabilization, requires monitoring. In the upper stratosphere, the modeled rate of HCl decline (2004–2017) is −5.2% per decade with VSLS included, in good agreement to ACE satellite data (−4.8% per decade), and 15% slower than a model simulation without VSLS. Thus, VSLS have offset a portion of stratospheric chlorine reductions since the mid‐2000s.
American Geophysical Union (AGU)
2019
Munksgaard Forlag
2019
2019
2019
Pergamon Press
2019
2019
Science Press
2019
2019
2019
Carbonaceous aerosol (total carbon, TCp) was source apportioned at nine European rural background sites, as part of the European Measurement and Evaluation Programme (EMEP) Intensive Measurement Periods in fall 2008 and winter/spring 2009. Five predefined fractions were apportioned based on ambient measurements: elemental and organic carbon, from combustion of biomass (ECbb and OCbb) and from fossil-fuel (ECff and OCff) sources, and remaining non-fossil organic carbon (OCrnf), dominated by natural sources.
OCrnf made a larger contribution to TCp than anthropogenic sources (ECbb, OCbb, ECff, and OCff) at four out of nine sites in fall, reflecting the vegetative season, whereas anthropogenic sources dominated at all but one site in winter/spring. Biomass burning (OCbb + ECbb) was the major anthropogenic source at the central European sites in fall, whereas fossil-fuel (OCff + ECff) sources dominated at the southernmost and the two northernmost sites. Residential wood burning emissions explained 30 %–50 % of TCp at most sites in the first week of sampling in fall, showing that this source can be the dominant one, even outside the heating season. In winter/spring, biomass burning was the major anthropogenic source at all but two sites, reflecting increased residential wood burning emissions in the heating season. Fossil-fuel sources dominated EC at all sites in fall, whereas there was a shift towards biomass burning for the southernmost sites in winter/spring.
Model calculations based on base-case emissions (mainly officially reported national emissions) strongly underpredicted observational derived levels of OCbb and ECbb outside Scandinavia. Emissions based on a consistent bottom-up inventory for residential wood burning (and including intermediate volatility compounds, IVOCs) improved model results compared to the base-case emissions, but modeled levels were still substantially underestimated compared to observational derived OCbb and ECbb levels at the southernmost sites.
Our study shows that natural sources are a major contributor to carbonaceous aerosol in Europe, even in fall and in winter/spring, and that residential wood burning emissions are equally as large as or larger than that of fossil-fuel sources, depending on season and region. The poorly constrained residential wood burning emissions for large parts of Europe show the obvious need to improve emission inventories, with harmonization of emission factors between countries likely being the most important step to improve model calculations for biomass burning emissions, and European PM2.5 concentrations in general.
2019
Arctic-breeding geese acquire resources for egg production from overwintering and breeding grounds, where pollutant exposure may differ. We investigated the effect of migration strategy on pollutant occurrence of lipophilic polychlorinated biphenyls (PCBs) and protein-associated poly- and perfluoroalkyl substances (PFASs) and mercury (Hg) in eggs of herbivorous barnacle geese (Branta leucopsis) from an island colony on Svalbard. Stable isotopes (δ13C and δ15N) in eggs and vegetation collected along the migration route were similar. Pollutant concentrations in eggs were low, reflecting their terrestrial diet (∑PCB = 1.23 ± 0.80 ng/g ww; ∑PFAS = 1.21 ± 2.97 ng/g ww; Hg = 20.17 ± 7.52 ng/g dw). PCB concentrations in eggs increased with later hatch date, independently of lipid content which also increased over time. Some females may remobilize and transfer more PCBs to their eggs, by delaying migration several weeks, relying on more polluted and stored resources, or being in poor body condition when arriving at the breeding grounds. PFAS and Hg occurrence in eggs did not change throughout the breeding season, suggesting migration has a greater effect on lipophilic pollutants. Pollutant exposure during offspring production in Arctic-breeding migrants may result in different profiles, with effects becoming more apparent with increasing trophic levels.
2019
2019