Comparison of PM2.5 chemical composition and sources at a rural background site in Central Europe between 1993/1994/1995 and 2009/2010: Effect of legislative regulations and economic transformation on the air quality

2018 ◽  
Vol 241 ◽  
pp. 841-851 ◽  
Author(s):  
Petra Pokorná ◽  
Jaroslav Schwarz ◽  
Radovan Krejci ◽  
Erik Swietlicki ◽  
Vladimír Havránek ◽  
...  
Atmosphere ◽  
2019 ◽  
Vol 10 (11) ◽  
pp. 687 ◽  
Author(s):  
Radek Lhotka ◽  
Petra Pokorná ◽  
Naděžda Zíková

An increased burden due to polycyclic aromatic hydrocarbons (PAH) is a long-term air quality problem in Central and Eastern Europe. Extensive PAH monitoring has been implemented at the National Atmospheric Observatory Košetice (NAOK), a rural background site in the Czech Republic, as a representative for Central Europe. Data from NAOK are used for evaluation of PAH concentration trends and source apportionment. In total, concentrations of 14 PAHs in particulate matter (PM10) and in the gas phase between 2006 and 2016 were evaluated. The highest concentrations were measured at the beginning of the study period in 2006. Mean annual concentrations of benzo(a)pyrene, for example, showed a weak, however statistically significant decreasing trend. The positive matrix factorization (PMF) was used to determine the sources of PAHs at NAOK, with three factors resolved. The probable origin areas of PMF factors were identified by the conditional bivariate probability function (CBPF) and the potential source contribution function (PSCF) methods. The NAOK is affected by local sources of PAHs, as well as by regional and long-range transport. The PAH concentrations correlate negatively with industrial production and traffic intensity. High PAH emissions have been linked to local heating, suggesting that the planned replacement of obsolete combustion sources in the households could improve the overall air quality situation, not only with respect to PAHs.


2016 ◽  
Vol 176-177 ◽  
pp. 108-120 ◽  
Author(s):  
Jaroslav Schwarz ◽  
Michael Cusack ◽  
Jindřich Karban ◽  
Eva Chalupníčková ◽  
Vladimír Havránek ◽  
...  

2016 ◽  
Author(s):  
M. Bressi ◽  
F. Cavalli ◽  
C. A. Belis ◽  
J.-P. Putaud ◽  
R. Fröhlich ◽  
...  

Abstract. Fine particulate matter (PM) levels and resulting impacts on human health are in the Po Valley (Italy) among the highest in Europe. To build effective PM abatement strategies, it is necessary to characterize fine PM chemical composition, sources and atmospheric processes on long time scales (> months), with short time resolution (< day), and with particular emphasis on the predominant organic fraction. Although previous studies have been conducted in this region, none of them addressed all these aspects together. For the first time in the Po Valley, we investigate the chemical composition of non-refractory submicron PM (NR-PM1) with a time-resolution of 30 minutes at the regional background site of Ispra during one full year, using an Aerosol Chemical Speciation Monitor (ACSM) under the most up-to-date and stringent quality assurance protocol. The identification of the main components of the organic fraction is made using the Multilinear-Engine 2 algorithm implemented within the latest version of the SoFi toolkit. In addition, with a view of a potential implementation of ACSM measurements in European air quality networks as a replacement of traditional filter-based techniques, parallel multiple off-line analyses were carried out to assess the performance of the ACSM in the determination of PM chemical species regulated by Air Quality Directives. The annual NR-PM1 level monitored at the study site (14.2 µg/m3) is among the highest in Europe, and is even comparable to levels reported in urban areas like New York City (USA, 14.2 µg/m3) and Tokyo (Japan, 12–15 µg/m3). On the annual basis, submicron particles are primarily composed of organic aerosol (OA, 58 % of NR-PM1). This fraction was apportioned into oxygenated OA (OOA, 66 %), hydrocarbon-like OA (HOA, 11 % of OA), and biomass burning OA (BBOA, 23 %). Among the primary sources of OA, biomass burning (23 %) is thus bigger than fossil fuel combustion (11 %). Significant contributions of aged secondary organic aerosol (OOA) are observed throughout the year. The unexpectedly high degree of oxygenation estimated during wintertime is probably due to the contribution of secondary BBOA and the enhancement of aqueous phase production of OOA during cold months. BBOA and nitrate are the only components of which contributions increase with the NR-PM1 levels. Therefore, biomass burning and NOx emission reductions would be particularly efficient in limiting submicron aerosol pollution events. Abatement strategies conducted during cold seasons appear to be more efficient than annual-based policies. In a broader context, further studies using high-time resolution analytical techniques on a long-term basis for the characterization of fine aerosol should help better shape our future air quality policies, which constantly need refinement.


2018 ◽  
Vol 182 ◽  
pp. 335-346 ◽  
Author(s):  
Saliou Mbengue ◽  
Michal Fusek ◽  
Jaroslav Schwarz ◽  
Petr Vodička ◽  
Adéla Holubová Šmejkalová ◽  
...  

2016 ◽  
Vol 16 (20) ◽  
pp. 12875-12896 ◽  
Author(s):  
Michael Bressi ◽  
Fabrizia Cavalli ◽  
Claudio A. Belis ◽  
Jean-Philippe Putaud ◽  
Roman Fröhlich ◽  
...  

Abstract. Fine particulate matter (PM) levels and resulting impacts on human health are in the Po Valley (Italy) among the highest in Europe. To build effective PM abatement strategies, it is necessary to characterize fine PM chemical composition, sources and atmospheric processes on long timescales (> months), with short time resolution (< day), and with particular emphasis on the predominant organic fraction. Although previous studies have been conducted in this region, none of them addressed all these aspects together. For the first time in the Po Valley, we investigate the chemical composition of nonrefractory submicron PM (NR-PM1) with a time resolution of 30 min at the regional background site of Ispra during 1 full year, using the Aerodyne Aerosol Chemical Speciation Monitor (ACSM) under the most up-to-date and stringent quality assurance protocol. The identification of the main components of the organic fraction is made using the Multilinear-Engine 2 algorithm implemented within the latest version of the SoFi toolkit. In addition, with the aim of a potential implementation of ACSM measurements in European air quality networks as a replacement of traditional filter-based techniques, parallel multiple offline analyses were carried out to assess the performance of the ACSM in the determination of PM chemical species regulated by air quality directives. The annual NR-PM1 level monitored at the study site (14.2 µg m−3) is among the highest in Europe and is even comparable to levels reported in urban areas like New York City and Tokyo. On the annual basis, submicron particles are primarily composed of organic aerosol (OA, 58 % of NR-PM1). This fraction was apportioned into oxygenated OA (OOA, 66 %), hydrocarbon-like OA (HOA, 11 % of OA) and biomass burning OA (BBOA, 23 %). Among the primary sources of OA, biomass burning (23 %) is thus bigger than fossil fuel combustion (11 %). Significant contributions of aged secondary organic aerosol (OOA) are observed throughout the year. The unexpectedly high degree of oxygenation estimated during wintertime is probably due to the contribution of secondary BBOA and the enhancement of aqueous-phase production of OOA during cold months. BBOA and nitrate are the only components of which contributions increase with the NR-PM1 levels. Therefore, biomass burning and NOx emission reductions would be particularly efficient in limiting submicron aerosol pollution events. Abatement strategies conducted during cold seasons appear to be more efficient than annual-based policies. In a broader context, further studies using high-time-resolution analytical techniques on a long-term basis for the characterization of fine aerosol should help better shape our future air quality policies, which constantly need refinement.


2001 ◽  
Vol 35 (10) ◽  
pp. 1853-1862 ◽  
Author(s):  
Andreas Limbeck ◽  
Hans Puxbaum ◽  
Luanne Otter ◽  
Mary C. Scholes

2021 ◽  
Vol 21 (18) ◽  
pp. 13931-13971
Author(s):  
Volker Matthias ◽  
Markus Quante ◽  
Jan A. Arndt ◽  
Ronny Badeke ◽  
Lea Fink ◽  
...  

Abstract. The lockdown measures taken to prevent a rapid spreading of the coronavirus in Europe in spring 2020 led to large emission reductions, particularly in road traffic and aviation. Atmospheric concentrations of NO2 and PM2.5 were mostly reduced when compared to observations taken for the same time period in previous years; however, concentration reductions may not only be caused by emission reductions but also by specific weather situations. In order to identify the role of emission reductions and the meteorological situation for air quality improvements in central Europe, the meteorology chemistry transport model system COSMO-CLM/CMAQ was applied to Europe for the period 1 January to 30 June 2020. Emission data for 2020 were extrapolated from most recent reported emission data, and lockdown adjustment factors were computed from reported activity data changes, e.g. Google mobility reports. Meteorological factors were investigated through additional simulations with meteorological data from previous years. The results showed that lockdown effects varied significantly among countries and were most prominent for NO2 concentrations in urban areas with 2-week-average reductions up to 55 % in the second half of March. Ozone concentrations were less strongly influenced (up to ±15 %) and showed both increasing and decreasing concentrations due to lockdown measures. This depended strongly on the meteorological situation and on the NOx / VOC emission ratio. PM2.5 revealed 2 %–12 % reductions of 2-week-average concentrations in March and April, which is much less than a different weather situation could cause. Unusually low PM2.5 concentrations as observed in northern central Europe were only marginally caused by lockdown effects. The lockdown can be seen as a big experiment about air quality improvements that can be achieved through drastic traffic emission reductions. From this investigation, it can be concluded that NO2 concentrations can be largely reduced, but effects on annual average values are small when the measures last only a few weeks. Secondary pollutants like ozone and PM2.5 depend more strongly on weather conditions and show a limited response to emission changes in single sectors.


2011 ◽  
Vol 11 (7) ◽  
pp. 20575-20629
Author(s):  
S. Basart ◽  
M. T. Pay ◽  
O. Jorba ◽  
C. Pérez ◽  
P. Jiménez-Guerrero ◽  
...  

Abstract. The CALIOPE high-resolution air quality modelling system is developed and applied to Europe (12 km × 12 km, 1 h). The modelled daily to seasonal aerosol variability over Europe in 2004 have been evaluated and analysed. The aerosols are estimated from two models, CMAQv4.5 (AERO4) and BSC-DREAM8b. CMAQv4.5 calculates biogenic, anthropogenic and sea salt aerosol and BSC-DREAM8b provides the natural mineral dust contribution from North African deserts. For the evaluation, we use daily PM10/PM2.5 and chemical composition data from 54 stations of the EMEP/CREATE network and coarse and fine aerosol optical depth (AOD) data from 35 stations of the AERONET sun photometer network. The model achieves daily PM10 and PM2.5 correlations of 0.57 and 0.47, respectively, and total, coarse and fine AOD correlations of 0.51, 0.63, and 0.53, respectively. The higher correlations of the PM10 and the coarse mode AOD are largely due to the accurate representation of the African dust influence in the forecasting system. Overall PM and AOD levels are underestimated. The evaluation of the chemical composition highlights underestimations of the modelled fine fractions particularly for carbonaceous matter (EC and OC) and secondary inorganic aerosols (SIA; i.e. nitrates, sulphates and ammonium). The scores of the bulk parameters are significantly improved after applying a simple model bias correction based on the chemical composition observations. SIA are dominant in the fine fractions representing up to 80 % of the aerosol budget in latitudes beyond 40° N. The highest aerosol concentrations are found over the industrialized and populated areas of the Po Valley and the Benelux regions. High values in southern Europe are linked to the transport of coarse particles from the Sahara desert which contributes up to 40 % of the total aerosol mass. Close to the surface, maxima dust seasonal concentrations (>30 μg m–3) are found between spring and early autumn. We estimate that desert dust causes daily exceedances of the PM10 European air quality threshold (50 μg m–3) in large areas south of 45° N reaching up to more than 75 days per year in the southernmost regions.


2021 ◽  
Vol 21 (18) ◽  
pp. 14199-14213
Author(s):  
John MacInnis ◽  
Jai Prakash Chaubey ◽  
Crystal Weagle ◽  
David Atkinson ◽  
Rachel Ying-Wen Chang

Abstract. The chemical composition, sources, and concentrations of aerosol particles vary on a seasonal basis in the Arctic. While existing research has focused on understanding the occurrence of aerosol particles during the Arctic winter and spring, less is known of their occurrence during the Arctic summer. In this study, atmospheric aerosol particle chemical composition and concentration were determined during July–September 2018 at Tuktoyaktuk, NT, Canada (69.4∘ N, 133.0∘ W), to coincide with the Year of Polar Prediction's Second Special Observing Period in the Arctic. The chemical composition of fine (PM2.5) and coarse (PM10–2.5) aerosol filter samples suggests the ocean, mineral and/or road dust, and combustion were sources of the sampled aerosol particles. Mass concentrations of PM2 and PM10, estimated from optical particle counter measurements, remained within a similar range during the study. However, elevated mass concentrations coincided with a festival in the community of Tuktoyaktuk, suggesting local human activity was an important source of aerosol particles. Mass concentrations of PM2, which promote negative health effects in humans, were significantly lower at Tuktoyaktuk than the national air quality standard recommended by the government of Canada. These measurements provide an important baseline to compare with future measurements associated with the assessment of aerosol chemistry and air quality in the Arctic.


2021 ◽  
Author(s):  
Simone M. Pieber ◽  
Dac-Loc Nguyen ◽  
Hendryk Czech ◽  
Stephan Henne ◽  
Nicolas Bukowiecki ◽  
...  

&lt;p&gt;Open biomass burning (BB) is a globally widespread phenomenon. The fires release pollutants, which are harmful for human and ecosystem health and alter the Earth's radiative balance. Yet, the impact of various types of BB on the global radiative forcing remains poorly constrained concerning greenhouse gas emissions, BB organic aerosol (OA) chemical composition and related light absorbing properties. Fire emissions composition is influenced by multiple factors (e.g., fuel and thereby vegetation-type, fuel moisture, fire temperature, available oxygen). Due to regional variations in these parameters, studies in different world regions are needed. Here we investigate the influence of seasonally recurring BB on trace gas concentration and air quality at the regional Global Atmosphere Watch (GAW) station Pha Din (PDI) in rural Northwestern Vietnam. PDI is located in a sparsely populated area on the top of a hill (1466 m a.s.l.) and is well suited to study the large-scale fires on the Indochinese Peninsula, whose pollution plumes are frequently transported towards the site [1]. We present continuous trace gas observations of CO&lt;sub&gt;2&lt;/sub&gt;, CH&lt;sub&gt;4&lt;/sub&gt;, CO, and O&lt;sub&gt;3&lt;/sub&gt; conducted at PDI since 2014 and interpret the data with atmospheric transport simulations. Annually recurrent large scale BB leads to hourly time-scale peaks CO mixing ratios at PDI of 1000 to 1500 ppb around every April since the start of data collection in 2014. We complement this analysis with carbonaceous PM&lt;sub&gt;2.5 &lt;/sub&gt;chemical composition analyzed during an intensive campaign in March-April 2015. This includes measurements of elemental and organic carbon (EC/OC) and more than 50 organic markers, such as sugars, PAHs, fatty acids and nitro-aromatics [2]. For the intensive campaign, we linked CO, CO&lt;sub&gt;2&lt;/sub&gt;, CH&lt;sub&gt;4&lt;/sub&gt; and O&lt;sub&gt;3&lt;/sub&gt; mixing ratios to a statistical classification of BB events, which is based on OA composition. We found increased CO and O&lt;sub&gt;3&lt;/sub&gt; levels during medium and high BB influence during the intensive campaign. A backward trajectory analysis confirmed different source regions for the identified periods based on the OA cluster. Typically, cleaner air masses arrived from northeast, i.e., mainland China and Yellow sea during the intensive campaign. The more polluted periods were characterized by trajectories from southwest, with more continental recirculation of the medium cluster, and more westerly advection for the high cluster. These findings highlight that BB activities in Northern Southeast Asia significantly enhances the regional OA loading, chemical PM&lt;sub&gt;2.5 &lt;/sub&gt;composition and the trace gases in northwestern Vietnam. The presented analysis adds valuable data on air quality in a region of scarce data availability.&lt;/p&gt;&lt;p&gt;&amp;#160;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;REFERENCES&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;[1] Bukowiecki, N. et al. Effect of Large-scale Biomass Burning on Aerosol Optical Properties at the GAW Regional Station Pha Din, Vietnam. AAQR. 19, 1172&amp;#8211;1187 (2019).&lt;/p&gt;&lt;p&gt;[2] Nguyen, D. L, et al. Carbonaceous aerosol composition in air masses influenced by large-scale biomass burning: a case-study in Northwestern Vietnam. ACPD., https://doi.org/10.5194/acp-2020-1027, in review, 2020.&lt;/p&gt;


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