scholarly journals Impact of meteorological condition changes on air quality and particulate chemical composition during the COVID-19 lockdown

2021 ◽  
Vol 109 ◽  
pp. 45-56
Author(s):  
Jing Ding ◽  
Qili Dai ◽  
Yafei Li ◽  
Suqin Han ◽  
Yufen Zhang ◽  
...  
Keyword(s):  
Air Quality ◽  
Chemical Composition ◽  
Meteorological Condition

scholarly journals Aerosols in the CALIOPE air quality modelling system: validation and analysis of PM levels, optical depths and chemical composition over Europe

2011 ◽  
Vol 11 (7) ◽  
pp. 20575-20629
Author(s):  
S. Basart ◽  
M. T. Pay ◽  
O. Jorba ◽  
C. Pérez ◽  
P. Jiménez-Guerrero ◽  
...  
Keyword(s):  
Air Quality ◽  
Chemical Composition ◽  
Air Quality Modelling ◽  
Po Valley ◽  
Aerosol Mass ◽  
Forecasting System ◽  
Bulk Parameters ◽  
Quality Threshold ◽  
Daily Pm10 ◽  
Modelling System

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.

scholarly journals Measurement report: The chemical composition of and temporal variability in aerosol particles at Tuktoyaktuk, Canada, during the Year of Polar Prediction Second Special Observing Period

2021 ◽  
Vol 21 (18) ◽  
pp. 14199-14213
Author(s):  
John MacInnis ◽  
Jai Prakash Chaubey ◽  
Crystal Weagle ◽  
David Atkinson ◽  
Rachel Ying-Wen Chang
Keyword(s):  
Air Quality ◽  
Chemical Composition ◽  
Aerosol Particles ◽  
Road Dust ◽  
Quality Standard ◽  
The Arctic ◽  
Similar Range ◽  
The Government ◽  
Government Of Canada ◽  
Mass Concentrations

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.

Trace gases and organic aerosol at a rural site in Vietnam during large scale biomass burning

2021 ◽  
Author(s):  
Simone M. Pieber ◽  
Dac-Loc Nguyen ◽  
Hendryk Czech ◽  
Stephan Henne ◽  
Nicolas Bukowiecki ◽  
...  
Keyword(s):  
Air Quality ◽  
Chemical Composition ◽  
Biomass Burning ◽  
Large Scale ◽  
Trace Gases ◽  
Organic Aerosol ◽  
Trace Gas ◽  
Rural Site ◽  
Air Masses ◽  
Mixing Ratios

<p>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<sub>2</sub>, CH<sub>4</sub>, CO, and O<sub>3</sub> 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<sub>2.5 </sub>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<sub>2</sub>, CH<sub>4</sub> and O<sub>3</sub> mixing ratios to a statistical classification of BB events, which is based on OA composition. We found increased CO and O<sub>3</sub> 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<sub>2.5 </sub>composition and the trace gases in northwestern Vietnam. The presented analysis adds valuable data on air quality in a region of scarce data availability.</p><p> </p><p><strong>REFERENCES</strong></p><p>[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, 1172–1187 (2019).</p><p>[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.</p>

scholarly journals Transport of Po Valley aerosol pollution to the northwestern Alps – Part 2: Long-term impact on air quality

2019 ◽  
Author(s):  
Henri Diémoz ◽  
Gian Paolo Gobbi ◽  
Tiziana Magri ◽  
Giordano Pession ◽  
Sara Pittavino ◽  
...  
Keyword(s):  
Air Quality ◽  
Chemical Composition ◽  
Weather Prediction ◽  
Urban Site ◽  
Aerosol Layer ◽  
Aerosol Transport ◽  
Po Valley ◽  
Aerosol Mass Concentration ◽  
The Impact ◽  
Aerosol Properties

Abstract. This work evaluates the impact of trans-regional aerosol transport from the polluted Po basin on particulate matter levels (PM10) and physico-chemical characteristics in the northwestern Alps. To this purpose, we exploited a multi-sensor, multiplatform database over a 3-years period (2015–2017) accompanied by a series of numerical simulations. The experimental setup included operational (24/7) vertically-resolved aerosol profiles by an Automated LiDAR-Ceilometer (ALC), verticallyintegrated aerosol properties by a sun/sky photometer, and surface measurements of aerosol mass concentration, size distribution and chemical composition. This experimental set of observations was then complemented by modelling tools, including Numerical Weather Prediction (NWP), Trajectory Statistical (TSM) and Chemical Transport (CTM) models, plus Positive Matrix Factorisation (PMF) on both the PM10 chemical speciation analyses and size distributions. In a first companion study (Diémoz et al., 2019), we showed and discussed through detailed case studies the 4-D phenomenology of recurrent episodes of aerosol transport from the polluted Po basin to the northwestern Italian Alps, and particularly to the Aosta Valley. Here we draw more general and statistically significant conclusions on the frequency of occurrence of this phenomenon, and on the quantitative impact of this regular, wind-driven, aerosol-rich atmospheric tide on PM10 air quality levels in this alpine environment. Combining vertically-resolved ALC measurements with wind information, we found that an advected aerosol layer is observed at the receptor site (Aosta) in 93 % of days characterized by easterly winds (thermally-driven winds from the plain or synoptic circulation regimes), and that the longer the time spent by air masses over the Po plain the higher this probability. On a seasonal basis, frequency of advected aerosol layers from the Po basin maximises in summer (70 % of the days classified using the ALC profiles) and minimises in winter and spring (57 % of the classified days). Duration of these advection events ranges from few hours up to several days, while aerosol layer thickness ranges from 500 up to 4000 m. This phenomenon was found to largely impact both surface levels and column-integrated aerosol properties, with PM10 and AOD values respectively increasing up to a factor of 3.5 and 4 in dates under the Po Valley influence. Similar variations in PM10 values observed at different stations within the Aosta Valley also indicated the phenomenon to act at the regional scale and to be related to non-local emissions. Pollution transport events were also shown to modify the mean chemical composition and typical size of particles in the target region. In fact, increase in secondary species, and mainly nitrate- and sulfate-rich components, were found to be effective proxies of the advections, with the transported aerosol responsible for at least 25 % of the PM10 measured in the urban site of Aosta, and adding up to over 50 μg m−3 during specific episodes, thus exceeding alone the EU established daily limit. This percentage is expected to be higher in the rural, pristine areas on the northwestern Alps, where chemical data were not available and trans-boundary contribution to PM10 might thus exceed the local one. Advected aerosols were also found to be on average finer, more light-scattering and more hygroscopic than the locally-produced ones. From a modelling point of view, our CTM simulations performed over a full year showed that the model is able to reproduce the phenomenon but underestimates its impact on PM10 levels. As a sensitivity test, we employed the ALC-derived identification of aerosol advections to re-weight the emissions from outside the boundaries of the regional domain in order to match the observed PM10 field. This simplified exercise indicated that an increase of such external emissions by a factor of 4 in the model would reduce the PM10 mean bias forecasts error (MBE) from −10 μg m−3 to less than 2 μg m−3, the normalised mean standard deviation (NMSD) from over −50 % to less than −10 % and would halve the model PM10 maximum deviations.

scholarly journals Secondary Organic Aerosol from Atmospheric Photooxidation of Indole

2017 ◽  
Author(s):  
Julia Montoya ◽  
Jeremy R. Horne ◽  
Mallory L. Hinks ◽  
Lauren T. Fleming ◽  
Veronique Perraud ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Air Quality ◽  
Chemical Composition ◽  
High Resolution ◽  
Secondary Organic Aerosol ◽  
High Resolution Mass Spectrometry ◽  
Organic Aerosol ◽  
Scanning Mobility Particle Sizer ◽  
High Resolution Mass ◽  
Resolution Mass

Abstract. Indole is a heterocyclic compound emitted by various plant species under stressed conditions or during flowering events. The formation, optical properties, and chemical composition of secondary organic aerosol (SOA) formed by low-NOx photooxidation of indole were investigated. The SOA yield (1.1 ± 0.3) was estimated from measuring the particle mass concentration with a scanning mobility particle sizer (SMPS) and correcting it for the wall loss effects. The SOA particles were collected on filters and analysed offline with UV-Vis spectrophotometry to measure the mass absorption coefficient (MAC) of the bulk sample. The samples were visibly brown and had MAC values of ~7 m2/g at λ = 300 nm and ~2 m2/g at λ = 400 nm, comparable to strongly absorbing brown carbon emitted from biomass burning. The chemical composition of SOA was examined with several mass spectrometry methods. The direct analysis in real time mass spectrometry (DART-MS) and nanospray desorption electrospray high resolution mass spectrometry (nano-DESI-HRMS) were used to provide information about the overall distribution of SOA compounds. High performance liquid chromatography, coupled to photodiode array spectrophotometry and high resolution mass spectrometry (HPLC-PDA-HRMS) was used to identify chromophoric compounds. Indole derivatives, such as tryptanthrin, indirubin, indigo dye, and indoxyl red were found to contribute significantly to the visible absorption spectrum of indole SOA. The potential effect of indole SOA on air quality was explored with the airshed model, which found elevated concentrations of indole SOA during the afternoon hours contributing considerably to the total organic aerosol under selected scenarios. Because of its high MAC values, indole SOA can contribute to decreased visibility and poor air quality.

Chemical composition of rainwater and air quality in Zimbabwe, Africa

1994 ◽  
Vol 144 (1-3) ◽  
pp. 261-271 ◽  
Author(s):  
S.B. Jonnalagadda ◽  
J. Makadho ◽  
N. Matinde ◽  
R.P. Karimanzira ◽  
A. Makarau
Keyword(s):  
Air Quality ◽  
Chemical Composition

scholarly journals Elemental Chemical Composition, Size and Morphological Characterization of Individual Atmospheric Particles Within an Air Quality Program

2009 ◽  
Vol 15 (S2) ◽  
pp. 1300-1301 ◽  
Author(s):  
R Ramirez-Leal ◽  
HE Esparza-Ponce ◽  
A Varela-Sortillón ◽  
A Astorga-Reyes ◽  
A Roman-B
Keyword(s):  
Air Quality ◽  
Chemical Composition ◽  
Morphological Characterization ◽  
Atmospheric Particles ◽  
Quality Program

Extended abstract of a paper presented at Microscopy and Microanalysis 2009 in Richmond, Virginia, USA, July 26 – July 30, 2009

scholarly journals Variations in the chemical composition of the submicron aerosol and in the sources of the organic fraction at a regional background site of the Po Valley (Italy)

2016 ◽  
Author(s):  
M. Bressi ◽  
F. Cavalli ◽  
C. A. Belis ◽  
J.-P. Putaud ◽  
R. Fröhlich ◽  
...  
Keyword(s):  
Air Quality ◽  
Chemical Composition ◽  
Biomass Burning ◽  
Time Resolution ◽  
Organic Aerosol ◽  
Organic Fraction ◽  
Submicron Aerosol ◽  
Po Valley ◽  
Background Site ◽  
Abatement Strategies

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.

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