Large contribution of water-insoluble secondary organic aerosols in the region of Paris (France) during wintertime

International audienceNear real-time measurements of carbonaceous aerosols were performed in fine aerosols for a 10-day period during winter at a suburban site of Paris (France). These measurements were performed using an OCEC Sunset Field instrument for elemental carbon (EC) and organic carbon (OC); a Particle-Into-Liquid-Sampler coupled with a Total Organic Carbon (PILS-TOC) instrument for water-soluble OC (WSOC); and a 7-lambda aethalometer for absorption. A successful comparison was performed with filter sampling performed in parallel for EC, OC, and WSOC, providing further confidence on the results obtained by the online analyzers. A modified version of the aethalometer model was used to derive hourly concentrations of 3 organic aerosol (OA) sources: fossil fuel, wood burning, and secondary. This source apportionment was validated for primary OA (fossil fuel, wood burning) using time-resolved measurements of specific tracers (including levoglucosan, water-soluble potassium and methanol for wood burning) and showed that secondary organic aerosols (SOA) were the most abundant OA species during our study. Water-soluble properties of these different OA sources were investigated from the reconstruction of experimentally determined water-soluble/insoluble OC. About 23% of WSOC was found to be of a secondary (photochemical) origin. A large fraction of SOA was assigned as water-insoluble and could originate from semi-volatile primary OA from wood burning and/or anthropogenic emissions. These results have been obtained at a typical suburban site in France and may be then representative of a larger European area. They bring new light on the commonly accepted idea that SOA is mainly water-soluble

Chemical composition and source apportionment of atmospheric aerosols on the Namibian coast

International audienceAbstract. The chemical composition of aerosols is of particular importance to assess their interactions with radiation, clouds and trace gases in the atmosphere and consequently their effects on air quality and the regional climate. In this study, we present the results of the first long-term dataset of the aerosol chemical composition at an observatory on the coast of Namibia, facing the south-eastern Atlantic Ocean. Aerosol samples in the mass fraction of particles smaller than 10 µm in aerodynamic diameter (PM10) were collected during 26 weeks between 2016 and 2017 at the ground-based Henties Bay Aerosol Observatory (HBAO; 22∘6′ S, 14∘30′ E; 30 m above mean sea level). The resulting 385 filter samples were analysed by X-ray fluorescence and ion chromatography for 24 inorganic elements and 15 water-soluble ions. Statistical analysis by positive matrix factorisation (PMF) identified five major components, sea salt (mass concentration: 74.7±1.9 %), mineral dust (15.7±1.4 %,), ammonium neutralised (6.1±0.7 %), fugitive dust (2.6±0.2 %) and industry (0.9±0.7 %). While the contribution of sea salt aerosol was persistent, as the dominant wind direction was south-westerly and westerly from the open ocean, the occurrence of mineral dust was episodic and coincided with high wind speeds from the south-south-east and the north-north-west, along the coastline. Concentrations of heavy metals measured at HBAO were higher than reported in the literature from measurements over the open ocean. V, Cd, Pb and Nd were attributed to fugitive dust emitted from bare surfaces or mining activities. As, Zn, Cu, Ni and Sr were attributed to the combustion of heavy oils in commercial ship traffic across the Cape of Good Hope sea route, power generation, smelting and other industrial activities in the greater region. Fluoride concentrations up to 25 µg m−3 were measured, as in heavily polluted areas in China. This is surprising and a worrisome result that has profound health implications and deserves further investigation. Although no clear signature for biomass burning could be determined, the PMF ammonium-neutralised component was described by a mixture of aerosols typically emitted by biomass burning, but also by other biogenic activities. Episodic contributions with moderate correlations between NO3-, nss-SO42- (higher than 2 µg m−3) and nss-K+ were observed, further indicative of the potential for an episodic source of biomass burning. Sea salt accounted for up to 57 % of the measured mass concentrations of SO42-, and the non-sea salt fraction was contributed mainly by the ammonium-neutralised component and small contributions from the mineral dust component. The marine biogenic contribution to the ammonium-neutralised component is attributed to efficient oxidation in the moist marine atmosphere of sulfur-containing gas phase emitted by marine phytoplankton in the fertile waters offshore in the Benguela Upwelling System. The data presented in this paper provide the first ever information on the temporal variability of aerosol concentrations in the Namibian marine boundary layer. This data also provide context for intensive observations in the area

Composition and variability of gaseous organic pollution in the port megacity of Istanbul: source attribution, emission ratios and inventory evaluation

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Volatile organic compounds sources in Paris in spring 2007. Part II: source apportionment using positive matrix factorisation

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Volatile organic compounds sources in Paris in spring 2007. Part I: qualitative analysis

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Continental pollution in the western Mediterranean basin: vertical profiles of aerosol and trace gases measured over the sea during TRAQA 2012 and SAFMED 2013

International audienceIn this study we present airborne observations of aerosol and trace gases obtained over the sea in the Western Mediterranean Basin during the TRAQA (TRansport and Air QuAlity) and SAFMED (Secondary Aerosol Formation in the MEDiterranean) campaigns in summers 2012 and 2013. A total of 23 vertical profiles were measured up to 5000 m a.s.l. over an extended area (40–45° N latitude and 2° W–12° E longitude) including the Gulf of Genoa, Southern France, the Gulf of Lion, and the Spanish coast. TRAQA and SAFMED successfully measured a wide range of meteorological conditions which favoured the pollution export from different sources located around the basin. Also, several events of dust outflows were measured during the campaigns. Observations from the present study indicate that continental pollution largely affects the Western Mediterranean both close to coastal regions and in the open sea as far as ~250 km from the coastline. Aerosol layers not specifically linked with Saharan dust outflows are distributed ubiquitously which indicates quite elevated levels of background pollution throughout the Western Basin. The measured aerosol scattering coefficient varies between ~20 and 120 M m−1, while carbon monoxide (CO) and ozone (O3) mixing ratios are in the range of 60–170 and 30–85 ppbv, respectively. Pollution reaches 3000–4000 m in altitude and presents a very complex and highly stratified structure characterized by fresh and aged layers both in the boundary layer and in the free troposphere. Within pollution plumes the measured particle concentration in the Aitken (0.004–0.1 μm) and accumulation (0.1–1.0 μm) modes is between $\sim 100$ and 5000–6000 s cm−3 (standard cm−3), which is comparable to the aerosol concentration measured in continental urban areas. Additionally, our measurements indicate the presence of highly concentrated Aitken layers (10 000–15 000 s cm−3) observed both close to the surface and in the free troposphere, possibly linked to the influence of new particle formation (NPF) episodes over the basin

Wood burning: A major source of Volatile Organic Compounds during wintertime in the Paris region

International audienceAuthor contribution BL wrote the original draft, led data collection and processing and led the analysis. VG designed the campaign, gave a deep review on the first draft and participated in analysis. JEP participated in data processing, discussed analysis and reviewed the paper. CH, AB and OP discussed analysis, reviewed the paper and provided data (Airparif measurements and emission inventory). GF and VM discussed analysis, reviewed the paper and provided data (LISA measurements). FT participated in data processing. NB and RSE participated in data collection. MD provided data (CO measurements). AF and FM were involved in the deployment and maintenance of the instruments at LISA. CG was the technical manager for the EPPI project at LISA, she managed the installation and maintenance of the instruments. PF was the scientific manager of the PEGASUS platform where the measurements were conducted at LISA, she was in charge of the coordination of the platform use and instruments setup. SK reviewed the paper, SK and MH provided data (mixed layer height). OF supervised aerosol in situ measurements at SIRTA and reviewed the paper

Three years of measurements of light-absorbing aerosols over coastal Namibia: seasonality, origin, and transport

International audienceContinuous measurements between July 2012 and December 2015 at the Henties Bay Aerosol Observatory (HBAO; 22 • S, 14 • 05 E), Namibia, show that, during the austral wintertime, transport of light-absorbing black carbon aerosols occurs at low level into the marine boundary layer. The average of daily concentrations of equivalent black carbon (eBC) over the whole sampling period is 53 (±55) ng m −3. Peak values above 200 ng m −3 and up to 800 ng m −3 occur seasonally from May to August, ahead of the dry season peak of biomass burning in southern Africa (August to October). Analysis of 3-day air mass back-trajectories show that air masses from the South Atlantic Ocean south of Henties Bay are generally cleaner than air having originated over the ocean north of Henties Bay, influenced by the outflow of the major biomass burning plume, and from the continent, where wildfires occur. Additional episodic peak concentrations, even for oceanic transport, indicate that pollution from distant sources in South Africa and maritime traffic along the Atlantic ship tracks could be important. While we expect the direct radiative effect to be negligible, the indirect effect on the microphysical properties of the stratocumulus clouds and the deposition to the ocean could be significant and deserve further investigation, specifically ahead of the dry season

Distribution, optical properties, and radiative effect of pollution aerosols in the western mediter- ranean basin from TRAQA and SAFMED airborne observations.

International audiencePollution aerosols strongly influence the composition of the western Mediterranean basin, but at present little is known on their distribution, optical properties and radiative effects. We report in this study in situ observations of pollution aerosol plumes obtained over the sea in the western Mediterranean during the TRAQA (TRansport and Air QuAlity) and the SAFMED (Secondary Aerosol Formation in the MEDiterranean) airborne campaigns in summers 2012 and 2013 (Di Biagio et al, 2015). The TRAQA and SAFMED flights explored an extended region of the western Mediterranean between 40°-45°N latitude and 2°W-12°E longitude including the Gulf of Genoa, Southern France, the Gulf of Lion, and the Spanish coasts. Measurements were performed over the sea at various distances from the coastline and up to 5000 m altitude. TRAQA and SAFMED successfully measured a wide range of meteorological conditions which favoured the pollution export from different sources around the basin

POLLURISK: AN INNOVATIVE EXPERIMENTAL PLATFORM TO INVESTIGATE HEALTH IMPACTS OF AIR QUALITY

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