Author: "Nicolas Bonnaire" / Search Limiters: Available in Library Collection - Searchworks@Jio Institute Digital Library Search Results

Your search keyword '"Nicolas Bonnaire"' showing total 32 results

Start Over Author "Nicolas Bonnaire" Search Limiters Available in Library Collection

32 results on '"Nicolas Bonnaire"'

1. NO2, BC and PM Exposure of Participants in the Polluscope Autumn 2019 Campaign in the Paris Region

Author: Laura Bouillon, Valérie Gros, Mohammad Abboud, Hafsa El Hafyani, Karine Zeitouni, Stéphanie Alage, Baptiste Languille, Nicolas Bonnaire, Jean-Marc Naude, Salim Srairi, Arthur Campos Y Sansano, and Anne Kauffmann
Subjects: personal exposure, air quality, Île-De-France, portable sensors, urban pollution, Chemical technology, TP1-1185
Abstract: The Polluscope project aims to better understand the personal exposure to air pollutants in the Paris region. This article is based on one campaign from the project, which was conducted in the autumn of 2019 and involved 63 participants equipped with portable sensors (i.e., NO2, BC and PM) for one week. After a phase of data curation, analyses were performed on the results from all participants, as well as on individual participants’ data for case studies. A machine learning algorithm was used to allocate the data to different environments (e.g., transportation, indoor, home, office, and outdoor). The results of the campaign showed that the participants’ exposure to air pollutants depended very much on their lifestyle and the sources of pollution that may be present in the vicinity. Individuals’ use of transportation was found to be associated with higher levels of pollutants, even when the time spent on transport was relatively short. In contrast, homes and offices were environments with the lowest concentrations of pollutants. However, some activities performed in indoor air (e.g., cooking) also showed a high levels of pollution over a relatively short period.
Published: 2023
Full Text: View/download PDF

2. Overview of the French Operational Network for In Situ Observation of PM Chemical Composition and Sources in Urban Environments (CARA Program)

Author: Olivier Favez, Samuël Weber, Jean-Eudes Petit, Laurent Y. Alleman, Alexandre Albinet, Véronique Riffault, Benjamin Chazeau, Tanguy Amodeo, Dalia Salameh, Yunjiang Zhang, Deepchandra Srivastava, Abdoulaye Samaké, Robin Aujay-Plouzeau, Arnaud Papin, Nicolas Bonnaire, Carole Boullanger, Mélodie Chatain, Florie Chevrier, Anaïs Detournay, Marta Dominik-Sègue, Raphaële Falhun, Céline Garbin, Véronique Ghersi, Guillaume Grignion, Gilles Levigoureux, Sabrina Pontet, Jérôme Rangognio, Shouwen Zhang, Jean-Luc Besombes, Sébastien Conil, Gaëlle Uzu, Joël Savarino, Nicolas Marchand, Valérie Gros, Caroline Marchand, Jean-Luc Jaffrezo, and Eva Leoz-Garziandia
Subjects: France, urban air quality, aerosol chemical composition, source apportionment, monitoring strategies, Meteorology. Climatology, QC851-999
Abstract: The CARA program has been running since 2008 by the French reference laboratory for air quality monitoring (LCSQA) and the regional monitoring networks, to gain better knowledge—at a national level—on particulate matter (PM) chemistry and its diverse origins in urban environments. It results in strong collaborations with international-level academic partners for state-of-the-art, straightforward, and robust results and methodologies within operational air quality stakeholders (and subsequently, decision makers). Here, we illustrate some of the main outputs obtained over the last decade, thanks to this program, regarding methodological aspects (both in terms of measurement techniques and data treatment procedures) as well as acquired knowledge on the predominant PM sources. Offline and online methods are used following well-suited quality assurance and quality control procedures, notably including inter-laboratory comparison exercises. Source apportionment studies are conducted using various receptor modeling approaches. Overall, the results presented herewith underline the major influences of residential wood burning (during the cold period) and road transport emissions (exhaust and non-exhaust ones, all throughout the year), as well as substantial contributions of mineral dust and primary biogenic particles (mostly during the warm period). Long-range transport phenomena, e.g., advection of secondary inorganic aerosols from the European continental sector and of Saharan dust into the French West Indies, are also discussed in this paper. Finally, we briefly address the use of stable isotope measurements (δ15N) and of various organic molecular markers for a better understanding of the origins of ammonium and of the different organic aerosol fractions, respectively.
Published: 2021
Full Text: View/download PDF

3. Sources and Geographical Origins of PM10 in Metz (France) Using Oxalate as a Marker of Secondary Organic Aerosols by Positive Matrix Factorization Analysis

Author: Jean-Eudes Petit, Cyril Pallarès, Olivier Favez, Laurent Y. Alleman, Nicolas Bonnaire, and Emmanuel Rivière
Subjects: receptor modelling, positive matrix factorization, trajectory analysis, oxalate, secondary organic aerosols, Meteorology. Climatology, QC851-999
Abstract: An original source apportionment study was conducted on atmospheric particles (PM10) collected in Metz, one of the largest cities of Eastern France. A Positive matrix factorization (PMF) analysis was applied to a sampling filter-based chemical dataset obtained for the April 2015 to January 2017 period. Nine factors were clearly identified, showing mainly contributions from anthropogenic sources of primary PM (19.2% and 16.1% for traffic and biomass burning, respectively) as well as secondary aerosols (12.3%, 14.5%, 21.8% for sulfate-, nitrate-, and oxalate-rich factors, respectively). Wood-burning aerosols exhibited strong temporal variations and contributed up to 30% of the PM mass fraction during winter, while primary traffic concentrations remained relatively constant throughout the year. These two sources are also the main contributors during observed PM10 pollution episodes. Furthermore, the dominance of the oxalate-rich factor among other secondary aerosol factors underlines the role of atmospheric processing to secondary organic aerosol loadings which are still poorly characterized in this region. Finally, Concentration-Weighted Trajectory (CWT) analysis were performed to investigate the geographical origins of the apportioned sources, notably illustrating a significant transport of both nitrate-rich and sulfate-rich factors from Northeastern Europe but also from the Balkan region.
Published: 2019
Full Text: View/download PDF

4. Personal Exposure to Black Carbon, Particulate Matter and Nitrogen Dioxide in the Paris Region Measured by Portable Sensors Worn by Volunteers

Author: Languille, Baptiste, Gros, Valérie, Nicolas, Bonnaire, Honoré, Cécile, Kaufmann, Anne, Zeitouni, Karine, Department of Chemistry [Oslo], Faculty of Mathematics and Natural Sciences [Oslo], University of Oslo (UiO)-University of Oslo (UiO), Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), AIRPARIF - Surveillance de la qualité de l'air en Île-de-France, Mairie de Paris, Données et algorithmes pour une ville intelligente et durable - DAVID (DAVID), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), ANR-15-CE22-0018,POLLUSCOPE,Observatoire participatif pour la surveillance de l'exposition individuelle à la pollution de l'air en lien avec la santé(2015), and European Project: 654109,H2020,H2020-INFRAIA-2014-2015,ACTRIS-2(2015)
Subjects: Nicolas, 010504 meteorology & atmospheric sciences, Health, Toxicology and Mutagenesis, mobile measurements, ambient monitoring, urban pollution, microenvironments, air quality, Île-de-France, TP1-1185, 010501 environmental sciences, Toxicology, Gros, 01 natural sciences, complex mixtures, Article, C, A, Zeitouni, 11. Sustainability, [SDU.ENVI]Sciences of the Universe [physics]/Continental interfaces, environment, ComputingMilieux_MISCELLANEOUS, 0105 earth and related environmental sciences, [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, Chemical Health and Safety, V, Chemical technology, Honoré, B, K. Personal Exposure to mobile measurements, Languille, 13. Climate action, Kaufmann
Abstract: Portable sensors have emerged as a promising solution for personal exposure (PE) measurement. For the first time in Île-de-France, PE to black carbon (BC), particulate matter (PM), and nitrogen dioxide (NO2) was quantified based on three field campaigns involving 37 volunteers from the general public wearing the sensors all day long for a week. This successful deployment demonstrated its ability to quantify PE on a large scale, in various environments (from dense urban to suburban, indoor and outdoor) and in all seasons. The impact of the visited environments was investigated. The proximity to road traffic (for BC and NO2), as well as cooking activities and tobacco smoke (for PM), made significant contributions to total exposure (up to 34%, 26%, and 44%, respectively), even though the time spent in these environments was short. Finally, even if ambient outdoor levels played a role in PE, the prominent impact of the different environments suggests that traditional ambient monitoring stations is not a proper surrogate for PE quantification.
Published: 2022

5. Detecting and Characterizing Particulate Organic Nitrates with an Aerodyne Long-ToF Aerosol Mass Spectrometer

Author: Frans Graeffe, Liine Heikkinen, Olga Garmash, Mikko Äijälä, James Allan, Anaïs Feron, Manuela Cirtog, Jean-Eudes Petit, Nicolas Bonnaire, Andrew Lambe, Olivier Favez, Alexandre Albinet, Leah R. Williams, Mikael Ehn, Tampere University, Physics, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Institut National de l'Environnement Industriel et des Risques (INERIS), and Institute for Atmospheric and Earth System Research (INAR)
Subjects: [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, Atmospheric Science, nitrate radicals, Uncertainty, Organo-nitrates, 114 Physical sciences, quantification, Space and Planetary Science, Geochemistry and Petrology, Quantification, Soa, organo-nitrates, SOA, Ams, Nitrate radicals, AMS, [SDU.ENVI]Sciences of the Universe [physics]/Continental interfaces, environment, uncertainty
Abstract: Particulate organic nitrate (pON) can be a major part of secondary organic aerosol (SOA) and is commonly quantified by indirect means from aerosol mass spectrometer (AMS) data. However, pON quantification remains challenging. Here, we set out to quantify and characterize pON in the boreal forest, through direct field observations at Station for Measuring Ecosystem Atmosphere Relationships (SMEAR) II in Hyytia''la'', Finland, and targeted single precursor laboratory studies. We utilized a long time-of-flight AMS (LToF-AMS) for aerosol chemical characterization, with a particular focus to identify CxHyOzN+ ("CHON+") fragments. We estimate that during springtime at SMEAR II, pON (including both the organic and nitrate part) accounts for similar to 10% of the particle mass concentration (calculated by the NO+/NO2+ method) and originates mainly from the NO3 radical oxidation of biogenic volatile organic compounds. The majority of the background nitrate aerosol measured is organic. The CHON+ fragment analysis was largely unsuccessful at SMEAR II, mainly due to low concentrations of the few detected fragments. However, our findings may be useful at other sites as we identified 80 unique CHON+ fragments from the laboratory measurements of SOA formed from NO3 radical oxidation of three pON precursors (beta-pinene, limonene, and guaiacol). Finally, we noted a significant effect on ion identification during the LToF-AMS high-resolution data processing, resulting in too many ions being fit, depending on whether tungsten ions (W+) were used in the peak width determination. Although this phenomenon may be instrument-specific, we encourage all (LTOF-) AMS users to investigate this effect on their instrument to reduce the possibility of incorrect identifications.
Published: 2022

6. Analysis and determination of secondary organic aerosol (SOA) tracers (markers) in particulate matter standard reference material (SRM 1649b, urban dust)

Author: Stephen A. Wise, Grazia Maria Lanzafame, Alexandre Albinet, Deepchandra Srivastava, Federica Nalin, Nicolas Bonnaire, Institut National de l'Environnement Industriel et des Risques (INERIS), Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Chimie Atmosphérique Expérimentale (CAE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), National Institute of Standards and Technology [Gaithersburg] (NIST), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), and Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)
Subjects: Air pollution, 02 engineering and technology, Quechers, medicine.disease_cause, Mass spectrometry, behavioral disciplines and activities, 01 natural sciences, Biochemistry, Analytical Chemistry, 11. Sustainability, medicine, [SDU.ENVI]Sciences of the Universe [physics]/Continental interfaces, environment, ComputingMilieux_MISCELLANEOUS, [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, 010401 analytical chemistry, Extraction (chemistry), Repeatability, Particulates, 021001 nanoscience & nanotechnology, 0104 chemical sciences, Aerosol, 13. Climate action, Environmental chemistry, Environmental science, Gas chromatography, 0210 nano-technology
Abstract: Secondary organic aerosol (SOA) accounts for a significant fraction of particulate matter (PM) in the atmosphere. Source identification, including the SOA fraction, is critical for the effective management of air pollution. Molecular SOA markers (tracers) are key compounds allowing the source apportionment of SOA using different methodologies. Therefore, accurate SOA marker measurements in ambient air PM are important. This study determined the concentrations of 12 key SOA markers (biogenic and anthropogenic) in the urban dust standard reference material available from the National Institute of Standards and Technology (NIST) (SRM 1649b). Two extraction procedures, sonication and QuEChERS-like (quick easy cheap effective rugged and safe), have been compared. Three research laboratories/institutes using two analytical techniques (gas chromatography/mass spectrometry (GC/MS) and ultra-high-pressure liquid chromatography/tandem mass spectrometry (HPLC/MS-MS)) carried out the analyses. The results obtained were all in good agreement, except for 2-methylerythritol. The analysis of this compound still seems to be challenging by both GC/MS (large injection repeatability) and HPLC/MS-MS (separation issues of both 2-methyltetrols: 2-methylthreitol and 2-methylerythritol). Possible inhomogeneity in the SRM for this compound could also explain the large discrepancies observed. Sonication and QuEChERS-like procedures gave comparable results for the extraction of the SOA markers showing that QuEChERS-like extraction is suitable for the analysis of SOA markers in ambient air PM. As this study provides, for the first time, indicative values in a reference material for typical SOA markers, the analysis of SRM 1649b (urban dust) could be used for quality control/assurance purposes. Graphical abstract.
Published: 2019

7. Supplementary material to 'Response of atmospheric composition to COVID-19 lockdown measures during Spring in the Paris region (France)'

Author: Jean-Eudes Petit, Jean-Charles Dupont, Olivier Favez, Valérie Gros, Yunjiang Zhang, Jean Sciare, Leïla Simon, François Truong, Nicolas Bonnaire, Tanguy Amodeo, Robert Vautard, and Martial Haeffelin
Published: 2021

8. Response of atmospheric composition to COVID-19 lockdown measures during Spring in the Paris region (France)

Author: Nicolas Bonnaire, Valérie Gros, Yunjiang Zhang, Jean-Charles Dupont, François Truong, Martial Haeffelin, Jean-Eudes Petit, Olivier Favez, Robert Vautard, Leila Simon, Tanguy Amodeo, Jean Sciare, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Institut Pierre-Simon-Laplace (IPSL (FR_636)), École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-École polytechnique (X)-Centre National d'Études Spatiales [Toulouse] (CNES)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Institut National de l'Environnement Industriel et des Risques (INERIS), Extrèmes : Statistiques, Impacts et Régionalisation (ESTIMR), H2020 Research Infrastructures, INFRA: 654109, European Commission, EC, Centre National de la Recherche Scientifique, CNRS, Seventh Framework Programme, FP7, Commissariat à l'Énergie Atomique et aux Énergies Alternatives, CEA, Financial support. This research has been supported by the Eu, European Project: 262254,EC:FP7:INFRA,FP7-INFRASTRUCTURES-2010-1,ACTRIS(2011), European Project: 654109,H2020,H2020-INFRAIA-2014-2015,ACTRIS-2(2015), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), and Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
Subjects: [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, Pollutant, Pollution, Ozone, media_common.quotation_subject, Particulates, Atmospheric sciences, Aerosol, chemistry.chemical_compound, Megacity, chemistry, 13. Climate action, 11. Sustainability, Environmental science, Air quality index, NOx, media_common
Abstract: Since early 2020, the COVID-19 pandemic has led to lockdowns at national scales. These lockdowns resulted in large cuts of atmospheric pollutant emissions, notably related to the vehicular traffic source where daily commuting of light-duty vehicles was almost completely stopped in numerous urban areas worldwide, especially during Spring 2020. As a result, air quality changed in manners that are still currently under investigation. Long-term in-situ monitoring of atmospheric composition provides, to this perspective, essential information. However, a robust quantitative assessment of the impact of lockdown measures on ambient concentrations is hindered by weather variability. Basic comparisons with previous years may thus be flawed, especially regarding secondary pollutants, whose concentrations strongly depends on meteorological conditions. In order to circumvent this difficulty, an innovative methodology has been developed. The Analog Application for Air Quality (A3Q) method is based on the comparison of each day of lockdown to a group of analog days having similar meteorological conditions. The A3Q method has been successfully evaluated and applied to a comprehensive in-situ dataset of primary and secondary pollutants obtained at the SIRTA observatory, a suburban background site of the Paris megacity (France). The overall slight decrease of PM1 concentrations (−14 %) compared to business-as-usual conditions conceals contrasting behaviours. Primary traffic tracers (NOx and traffic-related carbonaceous aerosols) dropped by 42–66 % during the lockdown period. Further, the A3Q method enabled us to characterize of changes triggered by NOx decreases. Particulate nitrate and secondary organic aerosols (SOA), two of the main springtime aerosol components in North-Western Europe, decreased by −45 % and −25 %, respectively. A NOx-relationship emphasizes the interest of NOx mitigation policies at the regional (i.e. city) scale, although long-range pollution advection sporadically overcompensated regional decreases. Variations of the oxidation state of SOA suggests discrepancies in SOA formation processes. At the same time, the expected ozone increase (+20 %) underlines the negative feedback of NO titration. These results provide a quasi-comprehensive observation-based insight on mitigation policies regarding air quality in future low-carbon urban areas.
Published: 2021

9. One-year measurements of secondary organic aerosol (SOA) markers in the Paris region (France): Concentrations, gas/particle partitioning and SOA source apportionment

Author: Nicolas Bonnaire, Gerhard Lammel, Laurent Y. Alleman, Deepchandra Srivastava, Pourya Shahpoury, Grazia Maria Lanzafame, Benjamin A. Musa Bandowe, Bertrand Bessagnet, F. Couvidat, Alexandre Albinet, Olivier Favez, Institut National de l'Environnement Industriel et des Risques (INERIS), Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Ecole nationale supérieure Mines-Télécom Lille Douai (IMT Lille Douai), Institut Mines-Télécom [Paris] (IMT), European Project: 262254,EC:FP7:INFRA,FP7-INFRASTRUCTURES-2010-1,ACTRIS(2011), European Project: 654109,H2020,H2020-INFRAIA-2014-2015,ACTRIS-2(2015), INERIS, Parc Technologique, ALATA BP 2 60550, Verneuil-en-Halatte, France, Max Planck Institute for Chemistry, Division of Atmospheric Chemistry, 55128 Mainz, Germany, Air Quality Research Division [Toronto], Environment and Climate Change Canada, Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Ecole nationale supérieure Mines-Télécom Lille Douai (IMT Nord Europe), Centre d'Enseignement et de Recherche en Environnement Atmosphérique (CEREA), École des Ponts ParisTech (ENPC)-EDF R&D (EDF R&D), EDF (EDF)-EDF (EDF), and Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
Subjects: Pollution, Environmental Engineering, 010504 meteorology & atmospheric sciences, media_common.quotation_subject, 010501 environmental sciences, behavioral disciplines and activities, 01 natural sciences, chemistry.chemical_compound, TRACER, Environmental Chemistry, Waste Management and Disposal, Isoprene, ComputingMilieux_MISCELLANEOUS, 0105 earth and related environmental sciences, media_common, Total organic carbon, Pinene, Particulates, Aerosol, chemistry, 13. Climate action, Environmental chemistry, [SDE]Environmental Sciences, Environmental science, Particle
Abstract: Twenty-five biogenic and anthropogenic secondary organic aerosol (SOA) markers have been measured over a one-year period in both gaseous and PM10 phases in the Paris region (France). Seasonal and chemical patterns were similar to those previously observed in Europe, but significantly different from the ones observed in America and Asia due to dissimilarities in source precursor emissions. Nitroaromatic compounds showed higher concentrations in winter due to larger emissions of their precursors originating from biomass combustion used for residential heating purposes. Among the biogenic markers, only isoprene SOA marker concentrations increased in summer while pinene SOA markers did not display any clear seasonal trend. The measured SOA markers, usually considered as semi-volatiles, were mainly associated to the particulate phase, except for the nitrophenols and nitroguaiacols, and their gas/particle partitioning (GPP) showed a low temperature and OM concentrations dependency. An evaluation of their GPP with thermodynamic model predictions suggested that apart from equilibrium partitioning between organic phase and air, the GPP of the markers is affected by processes suppressing volatility from a mixed organic and inorganic phase, such as enhanced dissolution in aerosol aqueous phase and non-equilibrium conditions. SOA marker concentrations were used to apportion secondary organic carbon (SOC) sources applying both, an improved version of the SOA-tracer method and positive matrix factorization (PMF) Total SOC estimations agreed very well between both models, except in summer and during a highly processed Springtime PM pollution event in which systematic underestimation by the SOA tracer method was evidenced. As a first approach, the SOA-tracer method could provide a reliable estimation of the average SOC concentrations, but it is limited due to the lack of markers for aged SOA together with missing SOA/SOC conversion fractions for several sources.
Published: 2021

10. Overview of the French Operational Network for In Situ Observation of PM Chemical Composition and Sources in Urban Environments (CARA Program)

Author: Joel Savarino, Jean-Eudes Petit, Gilles Levigoureux, Shouwen Zhang, Sabrina Pontet, Laurent Y. Alleman, Florie Chevrier, Carole Boullanger, Raphaële Falhun, Gaëlle Uzu, Jean-Luc Besombes, Nicolas Bonnaire, Samuël Weber, Deepchandra Srivastava, Abdoulaye Samaké, Dalia Salameh, Arnaud Papin, Valérie Gros, Véronique Riffault, Yunjiang Zhang, Anais Detournay, Caroline Marchand, Alexandre Albinet, Nicolas Marchand, Marta Dominik-Sègue, Céline Garbin, Mélodie Chatain, Eva Leoz-Garziandia, Véronique Ghersi, Sébastien Conil, Jérôme Rangognio, Tanguy Amodeo, Guillaume Grignion, Robin Aujay-Plouzeau, Jean-Luc Jaffrezo, Benjamin Chazeau, Olivier Favez, Institut National de l'Environnement Industriel et des Risques (INERIS), LCSQA - Laboratoire Central de Surveillance de la Qualité de l’Air, Institut des Géosciences de l’Environnement (IGE), Institut de Recherche pour le Développement (IRD)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP ), Université Grenoble Alpes (UGA), Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Ecole nationale supérieure Mines-Télécom Lille Douai (IMT Lille Douai), Institut Mines-Télécom [Paris] (IMT), Centre for Energy and Environment (CERI EE - IMT Nord Europe), Ecole nationale supérieure Mines-Télécom Lille Douai (IMT Nord Europe), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT), Laboratoire Chimie de l'environnement (LCE), Aix Marseille Université (AMU)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), AtmoSud, Madininair, Atmo Grand Est, Atmo Nouvelle-Aquitaine, Atmo Bourgogne Franche-Comté (ATMO BFC), Atmo Normandie, Air Breizh, Gwad'air, AIRPARIF - Surveillance de la qualité de l'air en Île-de-France, Qualitair Corse, Air Pays de la Loire, ATMO Auvergne-Rhône-Alpes (ATMO-AURA), LIG'AIR- Surveillance de la Qualité de l'Air en Région Centre, ATMO Hauts de France [Lille], Environnements, Dynamiques et Territoires de Montagne (EDYTEM), Université Savoie Mont Blanc (USMB [Université de Savoie] [Université de Chambéry])-Centre National de la Recherche Scientifique (CNRS), Observatoire Pérenne de l'Environnement, Agence Nationale pour la Gestion des Déchets Radioactifs (ANDRA), French Ministry of Environment, ADEME, CNRS, CEA, ACTRIS-France (CLAP national observation service), ANDRA, ENS Paris, CARA program (LCSQA), CPER CLIMIBIO, SOURCES project (1462C0064), DECOMBIO project (1362C0028), PM-DRIVE project (1162C0002), CAMERA project (1062c0008), INACS project (1262c0011), QAMECS project (1262c0011), ANR-11-LABX-0005,Cappa,Physiques et Chimie de l'Environnement Atmosphérique(2011), ANR-10-LABX-0056,OSUG@2020,Innovative strategies for observing and modelling natural systems(2010), European Project: 262254,EC:FP7:INFRA,FP7-INFRASTRUCTURES-2010-1,ACTRIS(2011), European Project: 654109,H2020,H2020-INFRAIA-2014-2015,ACTRIS-2(2015), Université Grenoble Alpes (UGA)-Centre National de la Recherche Scientifique (CNRS)-Institut national des sciences de l'Univers (INSU - CNRS)-Institut de Recherche pour le Développement (IRD)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP ), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Centre for Energy and Environment (CERI EE), Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU)-Institut de Chimie du CNRS (INC), Atmo Bourgogne Franche-Comté, Environnements, Dynamiques et Territoires de la Montagne (EDYTEM), and Centre National de la Recherche Scientifique (CNRS)-Université Savoie Mont Blanc (USMB [Université de Savoie] [Université de Chambéry])
Subjects: In situ, Atmospheric Science, source, 010504 meteorology & atmospheric sciences, [SDE.MCG]Environmental Sciences/Global Changes, Aerosol chemical composition, lcsh:QC851-999, 010501 environmental sciences, Environmental Science (miscellaneous), Mineral dust, Reference laboratory, 01 natural sciences, 7. Clean energy, apportionment, Apportionment, 11. Sustainability, Air quality index, Chemical composition, 0105 earth and related environmental sciences, [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, aerosol chemical composition, business.industry, Environmental resource management, Quality control, source apportionment, Particulates, atmospheric_science, Aerosol, monitoring strategies, 13. Climate action, urban air quality, Environmental chemistry, Environmental science, lcsh:Meteorology. Climatology, France, business, Quality assurance
Abstract: The CARA program has been developed since 2008 by the French reference laboratory for air quality monitoring (LCSQA) and the regional monitoring networks to gain a better knowledge at the national level on the particulate matter (PM) chemistry and its diverse origins in urban environments. It results of strong collaborations with international-level academic partners, allowing to bring state-of-the-art, straightforward and robust results and methodologies within operational air quality stakeholders (and subsequently, decision makers). Here, we illustrate some of the main outputs obtained over the last decade thanks to this program, regarding methodological aspects (both in terms of measurement techniques and data treatment procedures) as well as acquired knowledge on the predominant PM sources. Offline and online methods are used following well-suited quality assurance and quality control procedures, notably including inter-laboratory comparison exercises. Source apportionment studies are conducted using various receptor modeling approaches. Overall, the results presented herewith underline the major influences of residential wood burning (during the cold period) and road transport emissions (exhaust and non-exhaust ones, all along the year), as well as substantial contributions of mineral dust and primary biogenic particles (mostly during the warm period). Long-range transport phenomena, e.g., advection of secondary inorganic aerosols from the European continental sector and of Saharan dust into the French West Indies, are also discussed in this paper. Finally, we briefly address the use of stable isotope measurements (δ15N) and of various organic molecular markers for a better understanding of the origins of ammonium and of the different organic aerosol fractions, respectively.
Published: 2021

11. A methodology for the characterization of portable sensors for air quality measure with the goal of deployment in citizen science

Author: Cécile Honoré, Karine Zeitouni, Baptiste Languille, Nicolas Bonnaire, Valérie Gros, Clément Pommier, Laurent Gauvin, Isabella Annesi-Maesano, Christophe Debert, Basile Chaix, Salim Srairi, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), AIRPARIF - Surveillance de la qualité de l'air en Île-de-France, Centre d'Etudes et d'Expertise sur les Risques, l'Environnement, la Mobilité et l'Aménagement - Direction Ile-de-France (Cerema Direction Ile-de-France), Centre d'Etudes et d'Expertise sur les Risques, l'Environnement, la Mobilité et l'Aménagement (Cerema), Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Agence Nationale de la Recherche, ANR Horizon 2020 Framework Programme, H2020: 654109 Agence Nationale de la Recherche, ANR, This project was funded by the French agency: Agence nationale de la recherche (ANR – http://www.agencenationale-recherche.fr/Projet-ANR-15-CE22-0018). Part of the equipment was funded by iDEX Paris -Saclay, in the framework of the project ACE-ICSEN. Measurements from the SIRTA station were performed within the ACTRIS research infrastructure under the H2020 grant agreement 654109. Additional support from CEA and CNRS are acknowledged. Appendix A, ANR-15-CE22-0018,POLLUSCOPE,Observatoire participatif pour la surveillance de l'exposition individuelle à la pollution de l'air en lien avec la santé(2015), European Project: 654109,H2020,H2020-INFRAIA-2014-2015,ACTRIS-2(2015), Institut National de la Santé et de la Recherche Médicale (INSERM), Données et algorithmes pour une ville intelligente et durable - DAVID (DAVID), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM), HAL UVSQ, Équipe, Observatoire participatif pour la surveillance de l'exposition individuelle à la pollution de l'air en lien avec la santé - - POLLUSCOPE2015 - ANR-15-CE22-0018 - AAPG2015 - VALID, and Aerosols, Clouds, and Trace gases Research InfraStructure - ACTRIS-2 - - H20202015-05-01 - 2019-04-30 - 654109 - VALID
Subjects: Environmental Engineering, 010504 meteorology & atmospheric sciences, Computer science, Real-time computing, 010501 environmental sciences, 01 natural sciences, Black carbon, Air pollutants, Robustness (computer science), 11. Sustainability, Citizen science, [SDV.EE.SANT] Life Sciences [q-bio]/Ecology, environment/Health, Environmental Chemistry, Waste Management and Disposal, Air quality index, Nitrogen oxides, 0105 earth and related environmental sciences, [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, [SDV.EE.SANT]Life Sciences [q-bio]/Ecology, environment/Health, [SDE.IE]Environmental Sciences/Environmental Engineering, Paris region, Pollution, Ambient air, Personal exposure, [SDU]Sciences of the Universe [physics], Software deployment, [SDE.IE] Environmental Sciences/Environmental Engineering, Mobile measurements, Particulate matter
Abstract: International audience; The field of small air quality sensors is of growing interest within the scientific community, especially because this new technology is liable to improve air pollutant monitoring as well as be used for personal exposure quantification. Amongst the myriad existing devices, the performances are highly variable; this is why the sensors must be rigorously assessed before deployment, according to the intended use. This study is included in the Polluscope project; its purpose is to quantify personal exposure to air pollutants by using portable sensors. This paper designs and applies a methodology for the evaluation of portable air quality sensors to eight devices measuring PM, BC, NO2 and O3. The dedicated testing protocol includes static ambient air measurements compared with reference instruments, controlled chamber and mobility tests, as well as reproducibility evaluation. Three sensors (AE51, Cairclip and Canarin) were retained to be used for the field campaigns. The reliability of their performances were robustly quantified by using several metrics. These three devices (for a total of 36 units) were deployed to be worn by volunteers for a week. The results show the ability of sensors to discriminate between different environments (i.e., cooking, commuting or in an office). This work demonstrates, first, the ability of the three selected sensors to deliver data reliable enough to enable personal exposure estimations, and second, the robustness of this testing methodology.
Published: 2020

12. Characterization of particulate and gaseous pollutants from a French dairy and sheep farm

Author: Benjamin Loubet, Florence Lafouge, Brigitte Durand, Varunesh Chandra, Rachid Benabdallah, Julien Kammer, Oliver Fanucci, Céline Decuq, Nicolas Bonnaire, Pauline Buysse, Dominique Baisnée, Simona M. Cristescu, Jean-Eudes Petit, Raluca Ciuraru, François Truong, Ben Henderson, Sandy Bsaibes, Valérie Gros, Roland Sarda-Esteve, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Ecologie fonctionnelle et écotoxicologie des agroécosystèmes (ECOSYS), AgroParisTech-Université Paris-Saclay-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Chimie Atmosphérique Expérimentale (CAE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Department of Molecular and Laser Physics [Nijmegen], Institute for Molecules and Materials [Nijmegen], Radboud university [Nijmegen]-Radboud university [Nijmegen], ANAEE-France for the PTR-Qi-TOF-MS funding. The French Environment and Energy Management Agency ADEME for the funding through the AgriMultiPol program (17-03 C0012)., Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), and Radboud University [Nijmegen]-Radboud University [Nijmegen]
Subjects: VOC emissions, Environmental Engineering, 010504 meteorology & atmospheric sciences, Atmospheric pollution, 010501 environmental sciences, Residence time (fluid dynamics), 01 natural sciences, 7. Clean energy, chemistry.chemical_compound, Ammonia, Environmental Chemistry, Waste Management and Disposal, Air quality index, Chemical composition, 0105 earth and related environmental sciences, PTR-Qi-TOF-MS, Gaseous pollutants, Agriculture, Particulates, Pollution, chemistry, 13. Climate action, Environmental chemistry, Air quality, [SDE]Environmental Sciences, Carbon dioxide, Environmental science, Molecular and Laser Physics
Abstract: International audience; Agricultural activities highly contribute to atmospheric pollution, but the diversity and the magnitude of their emissions are still subject to large uncertainties. A field measurement campaign was conducted to characterize gaseous and particulate emissions from an experimental farm in France containing a sheep pen and a dairy stable. During the campaign, more than four hundred volatile organic compounds (VOCs) were characterized using an original combination of online and off-line measurements. Carbon dioxide (CO2) and ammonia (NH3) were the most concentrated compounds inside the buildings, followed by methanol, acetic acid and acetaldehyde. A CO2 mass balance model was used to estimate NH3 and VOC emission rates. To our knowledge, this study constitutes the first evaluation of emission rates for most of the identified VOCs. The measurements show that the dairy stable emitted more VOCs than the sheep pen. Despite strong VOC and NH3 emissions, the chemical composition of particles indicates that gaseous farm emissions do not affect the loading of fine particles inside the farm and is mainly explained by the low residence time inside the buildings. The experimental dataset obtained in this work will help to improve emissions inventories for agricultural activities.
Published: 2020

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

Author: Martial Haeffelin, Paola Formenti, Valérie Gros, Alexia Baudic, Roland Sarda-Esteve, Gilles Foret, Olivier Perrussel, Olivier Favez, Cécile Honoré, François Truong, Cécile Gaimoz, Nicolas Bonnaire, Simone Kotthaus, Marc Delmotte, Vincent Michoud, Anaïs Féron, Franck Maisonneuve, Jean-Eudes Petit, Baptiste Languille, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), AIRPARIF - Surveillance de la qualité de l'air en Île-de-France, Laboratoire Interuniversitaire des Systèmes Atmosphériques (LISA (UMR_7583)), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), ICOS-RAMCES (ICOS-RAMCES), Institut Pierre-Simon-Laplace (IPSL (FR_636)), École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-École polytechnique (X)-Centre National d'Études Spatiales [Toulouse] (CNES)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Institut National de l'Environnement Industriel et des Risques (INERIS), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), École normale supérieure - Paris (ENS Paris), and Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-École polytechnique (X)-Centre National d'Études Spatiales [Toulouse] (CNES)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP)
Subjects: [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, Data processing, Environmental Engineering, Data collection, 010504 meteorology & atmospheric sciences, 010501 environmental sciences, 01 natural sciences, Pollution, [SDU]Sciences of the Universe [physics], Environmental Chemistry, Wood burning, Environmental science, Emission inventory, Waste Management and Disposal, 0105 earth and related environmental sciences, Remote sensing
Abstract: Wood burning is widely used for domestic heating and has been identified as a ubiquitous pollution source in urban areas, especially during cold months. The present study is based on a three and a half winter months field campaign in the Paris region measuring Volatile Organic Compounds (VOCs) by Proton Transfer Reaction Mass Spectrometry (PTR-MS) in addition to Black Carbon (BC). Several VOCs were identified as strongly wood burning-influenced (e.g., acetic acid, furfural), or traffic-influenced (e.g., toluene, C8-aromatics). Methylbutenone, benzenediol and butandione were identified for the first time as wood burning-related in ambient air. A Positive Matrix Factorization (PMF) analysis highlighted that wood burning is the most important source of VOCs during the winter season. (47%). Traffic was found to account for about 22% of the measured VOCs during the same period, whereas solvent use plus background accounted altogether for the remaining fraction. The comparison with the regional emission inventory showed good consistency for benzene and xylenes but revisions of the inventory should be considered for several VOCs such as acetic acid, C9-aromatics and methanol. Finally, complementary measurements acquired simultaneously at other sites in Île-de-France (the Paris region) enabled evaluation of spatial variabilities. The influence of traffic emissions on investigated pollutants displayed a clear negative gradient from roadside to suburban stations, whereas wood burning pollution was found to be fairly homogeneous over the region.
Published: 2019

14. Sources and Geographical Origins of PM10 in Metz (France) Using Oxalate as a Marker of Secondary Organic Aerosols by Positive Matrix Factorization Analysis

Author: Cyril Pallares, Olivier Favez, Laurent Y. Alleman, Nicolas Bonnaire, Jean-Eudes Petit, Emmanuel Rivière, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Atmo Grand Est, Institut National de l'Environnement Industriel et des Risques (INERIS), LCSQA - Laboratoire Central de Surveillance de la Qualité de l’Air, Centre for Energy and Environment (CERI EE), Ecole nationale supérieure Mines-Télécom Lille Douai (IMT Lille Douai), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT), Institut Mines-Télécom [Paris] (IMT), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Centre for Energy and Environment (CERI EE - IMT Nord Europe), and Ecole nationale supérieure Mines-Télécom Lille Douai (IMT Nord Europe)
Subjects: Pollution, Atmospheric Science, 010504 meteorology & atmospheric sciences, media_common.quotation_subject, [SDE.MCG]Environmental Sciences/Global Changes, lcsh:QC851-999, 010501 environmental sciences, Environmental Science (miscellaneous), Atmospheric sciences, 01 natural sciences, chemistry.chemical_compound, receptor modelling, Nitrate, Dominance (ecology), Nonnegative matrix, secondary organic aerosols, Sulfate, Biomass burning, 0105 earth and related environmental sciences, media_common, oxalate, Secondary organic aerosols, Aerosol, chemistry, 13. Climate action, positive matrix factorization, Environmental science, lcsh:Meteorology. Climatology, trajectory analysis
Abstract: International audience; An original source apportionment study was conducted on atmospheric particles (PM 10) collected in Metz, one of the largest cities of Eastern France. A Positive matrix factorization (PMF) analysis was applied to a sampling filter-based chemical dataset obtained for the April 2015 to January 2017 period. Nine factors were clearly identified, showing mainly contributions from anthropogenic sources of primary PM (19.2% and 16.1% for traffic and biomass burning, respectively) as well as secondary aerosols (12.3%, 14.5%, 21.8% for sulfate-, nitrate-, and oxalate-rich factors, respectively). Wood-burning aerosols exhibited strong temporal variations and contributed up to 30% of the PM mass fraction during winter, while primary traffic concentrations remained relatively constant throughout the year. These two sources are also the main contributors during observed PM 10 pollution episodes. Furthermore, the dominance of the oxalate-rich factor among other secondary aerosol factors underlines the role of atmospheric processing to secondary organic aerosol loadings which are still poorly characterized in this region. Finally, Concentration-Weighted Trajectory (CWT) analysis were performed to investigate the geographical origins of the apportioned sources, notably illustrating a significant transport of both nitrate-rich and sulfate-rich factors from Northeastern Europe but also from the Balkan region.
Published: 2019
Full Text: View/download PDF

15. Supplementary material to 'Six-year source apportionment of submicron organic aerosols from near-continuous measurements at SIRTA (Paris area, France)'

Author: Yunjiang Zhang, Olivier Favez, Jean-Eudes Petit, Francesco Canonaco, Francois Truong, Nicolas Bonnaire, Vincent Crenn, Tanguy Amodeo, Andre S. H. Prévôt, Jean Sciare, Valerie Gros, and Alexandre Albinet
Published: 2019

16. The second ACTRIS inter-comparison (2016) for Aerosol Chemical Speciation Monitors (ACSM): Calibration protocols and instrument performance evaluations

Author: David C. Green, Jean Sciare, Evelyn Freney, François Truong, Jean-Eudes Petit, Roland Sarda-Esteve, Olivier Favez, Harald Flentje, Philip Croteau, Vincent Crenn, Nicola Zanca, Minna Aurela, C. Carbone, André S. H. Prévôt, Iasonas Stavroulas, Yunjiang Zhang, Aikaterini Bougiatioti, Max Priestman, Marek Maasikmets, Valérie Gros, Tarvo Arumae, Esther Coz, Leah R. Williams, Alfred Wiedensohler, Nikolaos Mihalopoulos, Tanguy Amodeo, Jeni Vasilescu, Thomas Elste, Anna Tobler, Manjula R. Canagaratna, María Cruz Minguillón, Begoña Artíñano, Hartmut Herrmann, Andrés Alastuey, Nicolas Bonnaire, Laurent Poulain, Liine Heikkinen, Luminita Marmureanu, John T. Jayne, Ministerio de Economía y Competitividad (España), Alastuey, Andrés [0000-0002-5453-5495], Minguillón, María Cruz [0000-0002-5464-0391], Laboratoire de Météorologie Physique (LaMP), Institut national des sciences de l'Univers (INSU - CNRS)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS), Institut National de l'Environnement Industriel et des Risques (INERIS), Aerodyne Research Inc., Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Finnish Meteorological Institute (FMI), Institute for Environmental Research and Sustainable Development (IERSD), National Observatory of Athens (NOA), Centro de Investigaciones Energéticas Medioambientales y Tecnológicas [Madrid] (CIEMAT), Deutscher Wetterdienst [Offenbach] (DWD), Helsingin yliopisto = Helsingfors universitet = University of Helsinki, Leibniz-Institut für Troposphärenforschung (TROPOS), Leibniz Institute for Tropospheric Research (TROPOS), King‘s College London, Institute of Environmental Assessment and Water Research (IDAEA), Consejo Superior de Investigaciones Científicas [Madrid] (CSIC), Cyprus Institute (CyI), Paul Scherrer Institute (PSI), National Institute of Research and Development for Optoelectronics (INOE), Consiglio Nazionale delle Ricerche [Bologna] (CNR), Estonian Environmental Research Center, Tallinn, Estonia, Laboratory of Atmospheric Chemistry [Paul Scherrer Institute] (LAC), Alastuey, Andrés, Minguillón, María Cruz, Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), University of Helsinki, Department of Chemistry, and INAR Physics
Subjects: Research program, SUBMICRON AEROSOLS, 010504 meteorology & atmospheric sciences, EFFICIENCIES, 116 Chemical sciences, Library science, 010501 environmental sciences, 114 Physical sciences, 01 natural sciences, 7. Clean energy, Data treatment, Air quality monitoring, CHEMISTRY, Political science, Environmental Chemistry, media_common.cataloged_instance, General Materials Science, Cost action, Environmental impact assessment, AMS, FIELD, European union, ComputingMilieux_MISCELLANEOUS, 0105 earth and related environmental sciences, media_common, [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, Aerosols, Chemical speciation, Water-soluble ions, Pollution, 13. Climate action, ORIGINS, [SDE]Environmental Sciences, Jim Smith, Christian ministry, Haze, Particulate matter
Abstract: This work describes results obtained from the 2016 Aerosol Chemical Speciation Monitor (ACSM) intercomparison exercise performed at the Aerosol Chemical Monitor Calibration Center (ACMCC, France). Fifteen quadrupole ACSMs (Q_ACSM) from the European Research Infrastructure for the observation of Aerosols, Clouds and Trace gases (ACTRIS) network were calibrated using a new procedure that acquires calibration data under the same operating conditions as those used during sampling and hence gets information representative of instrument performance. The new calibration procedure notably resulted in a decrease in the spread of the measured sulfate mass concentrations, improving the reproducibility of inorganic species measurements between ACSMs as well as the consistency with co-located independent instruments. Tested calibration procedures also allowed for the investigation of artifacts in individual instruments, such as the overestimation of m/z 44 from organic aerosol. This effect was quantified by the m/z (mass-to-charge) 44 to nitrate ratio measured during ammonium nitrate calibrations, with values ranging from 0.03 to 0.26, showing that it can be significant for some instruments. The fragmentation table correction previously proposed to account for this artifact was applied to the measurements acquired during this study. For some instruments (those with high artifacts), this fragmentation table adjustment led to an “overcorrection” of the f44 (m/z 44/Org) signal. This correction based on measurements made with pure NH4NO3, assumes that the magnitude of the artifact is independent of chemical composition. Using data acquired at different NH4NO3 mixing ratios (from solutions of NH4NO3 and (NH4)2SO4) we observe that the magnitude of the artifact varies as a function of composition. Here we applied an updated correction, dependent on the ambient NO3 mass fraction, which resulted in an improved agreement in organic signal among instruments. This work illustrates the benefits of integrating new calibration procedures and artifact corrections, but also highlights the benefits of these intercomparison exercises to continue to improve our knowledge of how these instruments operate, and assist us in interpreting atmospheric chemistry. © 2019, © 2019 Author(s). Published with license by Taylor & Francis Group, LLC., Funding text #1 aLaboratoire de Météorologie Physique (LaMP), Aubiere, France; bInstitut National de l’Environnement Industriel et des Risques (INERIS), Verneuil-en-Halatte, France; cLaboratoire des Sciences du Climat et de l’Environnement (LSCE), CNRS-CEA-UVSQ, Gif-sur-Yvette, France; dAerodyne Research, Inc, Billerica, Massachusetts, USA; eEnvironment Energy and Water Research Center, The Cyprus Institute, Nicosia, Cyprus; fEstonian Environmental Research Center (EERC), Tallinn, Estonia; gFinnish meteorological institute (FMI), Helsinki, Finland; hIERSD, National Observatory of Athens, Athens, Greece; iDepartment of the Environment, Centre for Energy, Environment and Technology Research (CIEMAT), Madrid, Spain; jDeutscher Wetterdienst, Meteorologisches Observatorium Hohenpeißenberg, Hohenpeißenberg, Germany; kInstitute for Atmospheric and Earth System Research (INAR)/Physics, Faculty of Science, University of Helsinki, Helsinki, Finland; lLeibniz Institute for Tropospheric Research, Leipzig, Germany; mEnvironmental Research Group, MRC-HPA Centre for Environment and Health, King’s College London, London, United Kingdom; nInstitute of Environmental Assessment and Water Research (IDAEA-CSIC), Barcelona, Spain; oLaboratory of Atmospheric Chemistry, Paul Scherrer Institute, Villigen PSI, Switzerland; pNational Institute of R&D for Optoelectronics (INOE), Ilfov, Romania; qProambiente S.c.r.l CNR Research Area, Bologna, Italy Funding text #2 This project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 654109. The US Department of Energy Small Business Innovative Research program (award number DE-SC0017041) provided support for development of ACSM calibration procedures. CNRS, CEA, and INERIS are acknowledged for financial support of the ACMCC. The intercomparison campaign and the following data treatment have been conducted in collaboration with the French reference laboratory for air quality monitoring (LCSQA), funded by the French Ministry of Environment. COST action CA16109 Chemical On-Line cOmpoSition and Source Apportionment of fine aerosoLs COLOSSAL grant is gratefully acknowledged for the support of data workshops. M.C. Minguillón acknowledges the Ramón y Cajal fellowship awarded by the Spanish Ministry of Economy, Industry and Competitiveness. The CIEMAT participation has been partially funded by MINECO/AEI/FEDER, UE (CGL2017-85344-R and CGL2017-90884-REDT) and TIGAS-CM (Y2018/EMT- 5177) Project. PSI is grateful for financial support by the Federal Office for the Environment in Switzerland.
Published: 2019

17. Speciation of organic fractions does matter for aerosol source apportionment. Part 3: Combining off-line and on-line measurements

Author: Yunjiang Zhang, Nicolas Bonnaire, Olivier Favez, Uwayemi Sofowote, Eric Villenave, Philip K. Hopke, Valérie Gros, Alexandre Albinet, Emilie Perraudin, Deepchandra Srivastava, Jean-Eudes Petit, Institut National de l'Environnement Industriel et des Risques (INERIS), Environnements et Paléoenvironnements OCéaniques (EPOC), Observatoire aquitain des sciences de l'univers (OASU), Université Sciences et Technologies - Bordeaux 1 (UB)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Sciences et Technologies - Bordeaux 1 (UB)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-École Pratique des Hautes Études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS), Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Ontario Ministry of the Environment and Climate Change, Center for Air Resources Engineering and Science, Clarkson University, Potsdam, NY, USA, Department of Public Health Sciences, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA, European Project: 654109,H2020,H2020-INFRAIA-2014-2015,ACTRIS-2(2015), UMR 5805 Environnements et Paléoenvironnements Océaniques et Continentaux (EPOC), Université Sciences et Technologies - Bordeaux 1-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Sciences et Technologies - Bordeaux 1-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-École pratique des hautes études (EPHE), and Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
Subjects: Pollution, Aerosol chemical speciation monitor (ACSM), Environmental Engineering, Source apportionment, 010504 meteorology & atmospheric sciences, media_common.quotation_subject, 010501 environmental sciences, 01 natural sciences, GEOF, Environmental Chemistry, [CHIM]Chemical Sciences, Biomass burning, Waste Management and Disposal, 0105 earth and related environmental sciences, Time synchronization, media_common, Particulate matter (PM), Secondary organic aerosol (SOA), Chemical speciation, Molecular markers, Time resolution, Aerosol, 13. Climate action, Environmental chemistry, Mass spectrum, Environmental science, Off line
Abstract: International audience; he present study proposes an advanced methodology to refine the source apportionment of organic aerosol (OA). This methodology is based on the combination of offline and online datasets in a single Positive Matrix Factorization (PMF) analysis using the multilinear engine (ME-2) algorithm and a customized time synchronization procedure. It has been applied to data from measurements conducted in the Paris region (France) during a PM pollution event in March 2015. Measurements included OA ACSM (Aerosol Chemical Speciation Monitor) mass spectra and specific primary and secondary organic molecular markers from PM10 filters on their original time resolution (30 min for ACSM and 4 h for PM10 filters). Comparison with the conventional PMF analysis of the ACSM OA dataset (PMF-ACSM) showed very good agreement for the discrimination between primary and secondary OA fractions with about 75% of the OA mass of secondary origin. Furthermore, the use of the combined datasets allowed the deconvolution of 3 primary OA (POA) factors and 7 secondary OA (SOA) factors. A clear identification of the source/origin of 54% of the total SOA mass could be achieved thanks to specific molecular markers. Specifically, 28% of that fraction was linked to combustion sources (biomass burning and traffic emissions). A clear identification of primary traffic OA was also obtained using the PMF-combined analysis while PMF-ACSM only gave a proxy for this OA source in the form of total hydrocarbon-like OA (HOA) mass concentrations. In addition, the primary biomass burning-related OA source was explained by two OA factors, BBOA and OPOA-like BBOA. This new approach has showed undeniable advantages over the conventional approaches by providing valuable insights into the processes involved in SOA formation and their sources. However, the origins of highly oxidized SOA could not be fully identified due to the lack of specific molecular markers for such aged SOA.
Published: 2019

18. ACTRIS ACSM intercomparison – Part 1: Reproducibility of concentration and fragment results from 13 individual Quadrupole Aerosol Chemical Speciation Monitors (Q-ACSM) and consistency with co-located instruments

Author: Valérie Gros, Laurent Poulain, Stéphanie Verlhac, Nicolas Bonnaire, David C. Green, Philip Croteau, Ari Setyan, Jean-Eudes Petit, M. Bressi, Begoña Artíñano, Andrés Alastuey, Claudio A. Belis, Mikko Äijälä, Jean Sciare, Urs Baltensperger, Fabrizia Cavalli, Francesco Canonaco, Chris Rene Lunder, Roman Fröhlich, Esther Coz, María Cruz Minguillón, Hartmut Herrmann, Liine Heikkinen, John T. Jayne, Anna Ripoll, Véronique Riffault, Manjula R. Canagaratna, André S. H. Prévôt, Olivier Favez, Max Priestman, Alfred Wiedensohler, Michael J. Cubison, Dominique Baisnée, Vincent Crenn, Ettore Petralia, Colin D. O'Dowd, C. Carbone, Wenche Aas, Griša Močnik, Jurgita Ovadnevaite, Jay G. Slowik, Roland Sarda-Esteve, Johanna K. Esser-Gietl, Génie Civil et Environnemental (GCE), École des Mines de Douai (Mines Douai EMD), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT), Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université Paris-Saclay-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Centre National de la Recherche Scientifique (CNRS), Service de Radiologie [Créteil], CHI Créteil, Norwegian Institute for Air Research (NILU), Institute of Environmental Assessment and Water Research (IDAEA), Consejo Superior de Investigaciones Científicas [Spain] (CSIC), Centro de Investigaciones Energéticas Medioambientales y Tecnológicas [Madrid] (CIEMAT), Paul Scherrer Institute (PSI), JRC Institute for Environment and Sustainability (IES), European Commission - Joint Research Centre [Ispra] (JRC), Angewandte Physik, Universität Paderborn (UPB), National University of Ireland [Galway] (NUI Galway), Laboratoire de Physiologie des Poissons, Institut National de la Recherche Agronomique (INRA), Leibniz Institute for Tropospheric Research (TROPOS), Institut Mines-Télécom [Paris] (IMT), Aerodyne Research Inc., Institut de recherches sur la catalyse et l'environnement de Lyon (IRCELYON), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS), Department of Physics, Centre for Materials and Processes (CERI MP), Ecole nationale supérieure Mines-Télécom Lille Douai (IMT Lille Douai), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Chimie Atmosphérique Expérimentale (CAE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Consejo Superior de Investigaciones Científicas [Madrid] (CSIC), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC), Centre for Materials and Processes (CERI MP - IMT Nord Europe), Ecole nationale supérieure Mines-Télécom Lille Douai (IMT Nord Europe), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), and Université de Lyon-Université de Lyon-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Atmospheric Science, SUBMICRON AEROSOLS, Analytical chemistry, Environmental engineering, 114 Physical sciences, Chloride, chemistry.chemical_compound, Earthwork. Foundations, Nitrate, PARTICULATE MATTER, Calibration, medicine, Organic matter, lcsh:TA170-171, Sulfate, [SDU.ENVI]Sciences of the Universe [physics]/Continental interfaces, environment, ORGANIC AEROSOL, 1172 Environmental sciences, [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, chemistry.chemical_classification, Reproducibility, SIZE DISTRIBUTIONS, lcsh:TA715-787, TA715-787, lcsh:Earthwork. Foundations, METROPOLITAN-AREA, TA170-171, Particulates, MULTIWAVELENGTH AETHALOMETER, lcsh:Environmental engineering, Aerosol, DOWNTOWN ATLANTA, SOURCE APPORTIONMENT, chemistry, MASS-SPECTROMETER DATA, HIGH-RESOLUTION, medicine.drug
Abstract: As part of the European ACTRIS project, the first large Quadrupole Aerosol Chemical Speciation Monitor (Q-ACSM) intercomparison study was conducted in the region of Paris for 3 weeks during the late-fall - early-winter period (November-December 2013). The first week was dedicated to the tuning and calibration of each instrument, whereas the second and third were dedicated to side-by-side comparison in ambient conditions with co-located instruments providing independent information on submicron aerosol optical, physical, and chemical properties. Near real-time measurements of the major chemical species (organic matter, sulfate, nitrate, ammonium, and chloride) in the non-refractory submicron aerosols (NR-PM1) were obtained here from 13 Q-ACSM. The results show that these instruments can produce highly comparable and robust measurements of the NR-PM1 total mass and its major components. Taking the median of the 13 Q-ACSM as a reference for this study, strong correlations (r2 > 0.9) were observed systematically for each individual Q-ACSM across all chemical families except for chloride for which three Q-ACSMs showing weak correlations partly due to the very low concentrations during the study. Reproducibility expanded uncertainties of Q-ACSM concentration measurements were determined using appropriate methodologies defined by the International Standard Organization (ISO 17025, 1999) and were found to be 9, 15, 19, 28, and 36 % for NR-PM1, nitrate, organic matter, sulfate, and ammonium, respectively. However, discrepancies were observed in the relative concentrations of the constituent mass fragments for each chemical component. In particular, significant differences were observed for the organic fragment at mass-to-charge ratio 44, which is a key parameter describing the oxidation state of organic aerosol. Following this first major intercomparison exercise of a large number of Q-ACSMs, detailed intercomparison results are presented, along with a discussion of some recommendations about best calibration practices, standardized data processing, and data treatment.
Published: 2015

19. Speciation of organic fractions does matter for aerosol source apportionment. Part 2 : Intensive short-term campaign in the Paris area (France)

Author: Emilie Perraudin, Nicolas Bonnaire, Martial Haeffelin, Alexandre Albinet, Eric Villenave, Valérie Gros, Franco Lucarelli, Deepchandra Srivastava, Olivier Favez, Institut National de l'Environnement Industriel et des Risques (INERIS), Laboratoire de Physico -& Toxico Chimie des systèmes naturels (LPTC), Université Sciences et Technologies - Bordeaux 1-Centre National de la Recherche Scientifique (CNRS), Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Chimie Atmosphérique Expérimentale (CAE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Institut Pierre-Simon-Laplace (IPSL (FR_636)), École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris Diderot - Paris 7 (UPD7)-École polytechnique (X)-Centre National d'Études Spatiales [Toulouse] (CNES)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Université Paris-Saclay-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Centre National de la Recherche Scientifique (CNRS), École normale supérieure - Paris (ENS Paris)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris Diderot - Paris 7 (UPD7)-École polytechnique (X)-Centre National d'Études Spatiales [Toulouse] (CNES)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Université Sciences et Technologies - Bordeaux 1 (UB)-Centre National de la Recherche Scientifique (CNRS), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), and École normale supérieure - Paris (ENS-PSL)
Subjects: Pollution, Environmental Engineering, 010504 meteorology & atmospheric sciences, media_common.quotation_subject, MOLECULAR MARKERS, 010501 environmental sciences, 01 natural sciences, behavioral disciplines and activities, Apportionment, 11. Sustainability, Environmental Chemistry, SOA, Biomass burning, Waste Management and Disposal, 0105 earth and related environmental sciences, media_common, Total organic carbon, Primary (chemistry), PMF, AEROSOL, Aerosol, Speciation, SOURCE APPORTIONMENT, 13. Climate action, Environmental chemistry, [SDE]Environmental Sciences, Environmental science
Abstract: International audience; The present study aimed at performing PM10 source apportionment, using positive matrix factorization (PMF), based on filter samples collected every 4 h at a sub-urban station in the Paris region (France) during a PM pollution event in March 2015 (PM10 > 50 μg m−3 for several consecutive days). The PMF model allowed to deconvolve 11 source factors. The use of specific primary and secondary organic molecular markers favoured the determination of common sources such as biomass burning and primary traffic emissions, as well as 2 specific biogenic SOA (marine + isoprene) and 3 anthropogenic SOA (nitro-PAHs + oxy-PAHs + phenolic compounds oxidation) factors. This study is probably the first one to report the use of methylnitrocatechol isomers as well as 1-nitropyrene to apportion secondary OA linked to biomass burning emissions and primary traffic emissions, respectively. Secondary organic carbon (SOC) fractions were found to account for 47% of the total OC. The use of organic molecular markers allowed the identification of 41% of the total SOC composed of anthropogenic SOA (namely, oxy-PAHs, nitro-PAHs and phenolic compounds oxidation, representing 15%, 9%, 11% of the total OC, respectively) and biogenic SOA (marine + isoprene) (6% in total). Results obtained also showed that 35% of the total SOC originated from anthropogenic sources and especially PAH SOA (oxy-PAHs + nitro-PAHs), accounting for 24% of the total SOC, highlighting its significant contribution in urban influenced environments. Anthropogenic SOA related to nitro-PAHs and phenolic compounds exhibited a clear diurnal pattern with high concentrations during the night indicating the prominent role of night-time chemistry but with different chemical processes involved.
Published: 2018

20. Organic carbon at a remote site of the western Mediterranean Basin: composition, sources and chemistry during the ChArMEx SOP2 field experiment

Author: Vincent Michoud, Jean Sciare, Stéphane Sauvage, Sébastien Dusanter, Thierry Léonardis, Valérie Gros, Cerise Kalogridis, Nora Zannoni, Anaïs Féron, Jean-Eudes Petit, Vincent Crenn, Dominique Baisnée, Roland Sarda-Estève, Nicolas Bonnaire, Nicolas Marchand, H. Langley DeWitt, Jorge Pey, Aurélie Colomb, François Gheusi, Sonke Szidat, Iasonas Stavroulas, Agnès Borbon, and Nadine Locoge
Abstract: The ChArMEx (Chemistry and Aerosol Mediterranean Experiment) SOP2 (Special Observation Period 2) field campaign took place from 15 July to 05 August 2013 in the western Mediterranean basin, at Ersa a remote site in Cape Corsica. During the campaign more than 80 Volatile Organic Compounds (VOCs), including oxygenated species were measured by different online and offline techniques. At the same time an exhaustive description of the chemical composition of fine aerosols was performed. First we combined a back-trajectory analysis and an estimation of photochemical age to characterize air mass origins and chemical processing times, which confirmed the remote nature of the site. Therefore, low levels of anthropogenic VOCs (typically tens to hundreds of ppt for individual species) and black carbon (0.1–0.9 μg m
Published: 2017

21. Supplementary material to 'Organic carbon at a remote site of the western Mediterranean Basin: composition, sources and chemistry during the ChArMEx SOP2 field experiment'

Author: Vincent Michoud, Jean Sciare, Stéphane Sauvage, Sébastien Dusanter, Thierry Léonardis, Valérie Gros, Cerise Kalogridis, Nora Zannoni, Anaïs Féron, Jean-Eudes Petit, Vincent Crenn, Dominique Baisnée, Roland Sarda-Estève, Nicolas Bonnaire, Nicolas Marchand, H. Langley DeWitt, Jorge Pey, Aurélie Colomb, François Gheusi, Sonke Szidat, Iasonas Stavroulas, Agnès Borbon, and Nadine Locoge
Published: 2017

22. Multi-tracer approach to characterize domestic wood burning in Athens (Greece) during wintertime

Author: Pavlos Zarmpas, K. Bairachtari, Th. Maggos, Iasonas Stavroulas, Basil E. Psiloglou, Roland Sarda-Esteve, Nikos Mihalopoulos, Evangelos Gerasopoulos, L. Fourtziou, C. Theodosi, Jean Sciare, Eleni Liakakou, Nicolas Bonnaire, Aikaterini Bougiatioti, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), and Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
Subjects: [SDU.OCEAN]Sciences of the Universe [physics]/Ocean, Atmosphere, Atmospheric Science, 010504 meteorology & atmospheric sciences, Meteorology, Chemistry, Levoglucosan, Athens greece, 010501 environmental sciences, Atmospheric sciences, 01 natural sciences, 7. Clean energy, Atmosphere, chemistry.chemical_compound, Deposition (aerosol physics), 13. Climate action, TRACER, 11. Sustainability, Wood burning, Precipitation, Biomass burning, [SDU.ENVI]Sciences of the Universe [physics]/Continental interfaces, environment, ComputingMilieux_MISCELLANEOUS, 0105 earth and related environmental sciences, General Environmental Science
Abstract: During the last years the atmosphere of the Great Athens Area (GAA) and other Greek cities is burdened from extended residential biomass burning for heating purposes. In this work, a series of near real-time and off-line biomass burning tracers are analyzed during intense wood burning events in Athens. The measurements were conducted at an urban background site located in the center of Athens, and in the heart of wood burning activities (winter 2013–2014). The measured tracers include high resolution measurements of non-sea salt potassium (nss-K+), wood burning black carbon (BCwb), the m/z 60 fragment associated with levoglucosan and monosaccharide anhydrides (levoglucosan, mannosan and galactosan) determined on selected filter samples. The suitability of these tracers was evaluated when the prevailing meteorological conditions with low dispersion and deposition mechanisms (low wind speed, absence of precipitation) were associated with high biomass burning emissions at nighttime. During the severe smog periods, the levels of K+, BCwb, m/z 60 and levoglucosan were up to 2.2 μg m−3, 12.5 μg m−3, 3.4 μg m−3 and 8.6 μg m−3, respectively, higher by a factor of at least two, relatively to the non smog periods due to biomass burning. Correlations between biomass burning tracers as well as between monosaccharide anhydrides provided information about the type of material and wood being burned.
Published: 2017

23. A top-down approach of surface carbonyl sulfide exchange by a Mediterranean oak forest ecosystem in Southern France

Author: Benjamin Lebegue, Bernard Genty, V. Kazan, Valérie Gros, Michel Ramonet, Catherine Fernandez, Marc Delmotte, Ilja M. Reiter, J. Lathière, Cerise Kalogridis, Thierry Gauquelin, Nicolas Bonnaire, Benjamin Loubet, Sauveur Belviso, David Montagne, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Université Paris-Saclay-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Centre National de la Recherche Scientifique (CNRS), Ecosystèmes continentaux et risques environnementaux (ECCOREV), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Environnement et Grandes Cultures (EGC), AgroParisTech-Institut National de la Recherche Agronomique (INRA), Ecologie fonctionnelle et écotoxicologie des agroécosystèmes (ECOSYS), Institut National de la Recherche Agronomique (INRA)-AgroParisTech, Laboratoire de glaciologie et géophysique de l'environnement (LGGE), Observatoire des Sciences de l'Univers de Grenoble (OSUG), Université Savoie Mont Blanc (USMB [Université de Savoie] [Université de Chambéry])-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP)-Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA)-Université Joseph Fourier - Grenoble 1 (UJF)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)-Université Savoie Mont Blanc (USMB [Université de Savoie] [Université de Chambéry])-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP)-Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA)-Université Joseph Fourier - Grenoble 1 (UJF)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)-Centre National de la Recherche Scientifique (CNRS), Aix Marseille Université (AMU), Institut méditerranéen de biodiversité et d'écologie marine et continentale (IMBE), Centre National de la Recherche Scientifique (CNRS)-Institut de recherche pour le développement [IRD] : UMR237-Aix Marseille Université (AMU)-Avignon Université (AU), Institut de Biosciences et Biotechnologies d'Aix-Marseille (ex-IBEB) (BIAM), Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Laboratoire d'Ecophysiologie Moléculaire des Plantes (LEMP), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), ICOS-RAMCES (ICOS-RAMCES), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie Atmosphérique Expérimentale (CAE), Modelling the Earth Response to Multiple Anthropogenic Interactions and Dynamics (MERMAID), Avignon Université (AU)-Aix Marseille Université (AMU)-Institut de recherche pour le développement [IRD] : UMR237-Centre National de la Recherche Scientifique (CNRS), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Protéines de Protection des Végétaux (PPV), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Direction de Recherche Fondamentale (CEA) (DRF (CEA)), and Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)
Subjects: 0106 biological sciences, Atmospheric Science, 010504 meteorology & atmospheric sciences, [SDE.MCG]Environmental Sciences/Global Changes, Eddy covariance, 01 natural sciences, lcsh:Chemistry, chemistry.chemical_compound, Sunrise, Ecosystem, 0105 earth and related environmental sciences, Carbonyl sulfide, Primary production, 15. Life on land, lcsh:QC1-999, Deposition (aerosol physics), lcsh:QD1-999, chemistry, 13. Climate action, Climatology, Carbon dioxide, [SDE]Environmental Sciences, Environmental science, Ecosystem respiration, lcsh:Physics, 010606 plant biology & botany
Abstract: The role that soil, foliage, and atmospheric dynamics have on surface carbonyl sulfide (OCS) exchange in a Mediterranean forest ecosystem in southern France (the Oak Observatory at the Observatoire de Haute Provence, O3HP) was investigated in June of 2012 and 2013 with essentially a top-down approach. Atmospheric data suggest that the site is appropriate for estimating gross primary production (GPP) directly from eddy covariance measurements of OCS fluxes, but it is less adequate for scaling net ecosystem exchange (NEE) to GPP from observations of vertical gradients of OCS relative to CO2 during the daytime. Firstly, OCS and carbon dioxide (CO2) diurnal variations and vertical gradients show no net exchange of OCS at night when the carbon fluxes are dominated by ecosystem respiration. This contrasts with other oak woodland ecosystems of a Mediterranean climate, where nocturnal uptake of OCS by soil and/or vegetation has been observed. Since temperature, water, and organic carbon content of soil at the O3HP should favor the uptake of OCS, the lack of nocturnal net uptake would indicate that its gross consumption in soil is compensated for by emission processes that remain to be characterized. Secondly, the uptake of OCS during the photosynthetic period was characterized in two different ways. We measured ozone (O3) deposition velocities and estimated the partitioning of O3 deposition between stomatal and non-stomatal pathways before the start of a joint survey of OCS and O3 surface concentrations. We observed an increasing trend in the relative importance of the stomatal pathway during the morning hours and synchronous steep drops of mixing ratios of OCS (amplitude in the range of 60–100 ppt) and O3 (amplitude in the range of 15–30 ppb) after sunrise and before the break up of the nocturnal boundary layer. The uptake of OCS by plants was also characterized from vertical profiles. However, the time window for calculation of the ecosystem relative uptake (ERU) of OCS, which is a useful tool for partitioning measured NEE, was limited in June 2012 to a few hours after midday. This was due to the disruption of the vertical distribution of OCS by entrainment of OCS rich tropospheric air in the morning and because the vertical gradient of CO2 reverses when it is still light. Moreover, polluted air masses (up to 700 ppt of OCS) produced dramatic variation in atmospheric OCS ∕ CO2 ratios during the daytime in June 2013, further reducing the time window for ERU calculation.
Published: 2016

24. Initial studies into the characterisation of ripening stages of Emmental cheeses by mid-infrared spectroscopy

Author: Nicolas Bonnaire, Sandra Teresita Martín Del Campo, Daniel Picque, and Georges Corrieu
Subjects: Absorbance, Chromatography, Chemistry, Attenuated total reflection, Principal component analysis, Analytical chemistry, Infrared spectroscopy, Cheese ripening, Ripening, Spectroscopy, Biochemistry, Mid infrared spectroscopy, Food Science
Abstract: Experimental Emmental cheeses were analysed to evaluate the potential of mid-infrared spectroscopy to follow the ripening process. Cheeses were sampled at seven different ripening stages and were analysed. The infrared spectra were obtained by placing the cheese slices directly over the attenuated total reflectance crystal. Analysis of variance showed significant (P ≤ 0.05) absorbance changes between spectral sets in the regions assigned to vibrations of alcohol, amide and hydrocarbon chains. Principal component analysis (PCA) made it possible to describe four groups including samples ripened during 21, 27 and 34 days (G1), 51 and 58 days (G2), 65 days (G3) and the samples at the end of the ripening (mould opening, about 85 days) (G4). Using general discriminant analysis of spectral data, it is not possible to correctly distinguish samples according to seven dates of sampling, but samples belonging to the four groups identified by PCA are predicted well by the regression model.
Published: 2009

25. ACTRIS ACSM intercomparison – Part I: Reproducibility of concentration and fragment results from 13 individual Quadrupole Aerosol Chemical Speciation Monitors (Q-ACSM) and consistency with Time-of-Flight ACSM (ToF-ACSM), High Resolution ToF Aerosol Mass Spectrometer (HR-ToF-AMS) and other co-located instruments

Author: Vincent Crenn, Olivier Favez, W. Aas, Mikko Äijälä, L. Poulain, G. Močnik, Anna Ripoll, J. T. Jayne, J. K. Esser-Gietl, A. Wiedensohler, L. Heikkinen, Max Priestman, M. Canagaratna, Philip Croteau, María Cruz Minguillón, J. G. Slowik, Jean-Eudes Petit, Valérie Gros, V. Riffault, André S. H. Prévôt, David C. Green, A. Setyan, C. D. D. O'Dowd, C. Lunder, Roland Sarda-Esteve, Fabrizia Cavalli, C. A. Belis, M. Bressi, Dominique Baisnée, Stéphane Verlhac, M. J. Cubison, Esther Coz, Ettore Petralia, Jean Sciare, H. Herrmann, Jurgita Ovadnevaite, U. Baltensperger, F. Canonaco, C. Carbone, B. Artiñano, Nicolas Bonnaire, Andrés Alastuey, and Roman Fröhlich
Subjects: Reproducibility, Time of flight, Fragment (computer graphics), Chemical speciation, Consistency (statistics), Quadrupole, Analytical chemistry, Environmental science, Mass spectrometry, Aerosol
Abstract: As part of the European ACTRIS project, the first large Quadrupole Aerosol Chemical Speciation Monitor (Q-ACSM) intercomparison study was conducted in the region of Paris for three weeks during the late fall–early winter period (November–December 2013). The first week was dedicated to tuning and calibration of each instrument whereas the second and third were dedicated to side-by-side comparison in ambient conditions with co-located instruments providing independent information on submicron aerosol optical, physical and chemical properties. Near real-time measurements of the major chemical species (organic matter, sulfate, nitrate, ammonium and chloride) in the non-refractory submicron aerosols (NR-PM1) were obtained here from 13 Q-ACSM. The results show that these instruments can produce highly comparable and robust measurements of the NR-PM1 total mass and its major components. Taking the median of the 13 Q-ACSM as a reference for this study, strong correlations (r2 > 0.9) were observed systematically for each individual ACSM across all chemical families except for chloride for which three ACSMs showing weak correlations partly due to the very low concentrations during the study. Reproducibility expanded uncertainties of Q-ACSM concentration measurements were determined using appropriate methodologies defined by the International Standard Organization (ISO 17025) and were found to be of 9, 15, 19, 28 and 36 % for NR-PM1, nitrate, organic matter, sulfate and ammonium respectively. However, discrepancies were observed in the relative concentrations of the constituent mass fragments for each chemical component. In particular, significant differences were observed for the organic fragment at mass-to-charge ratio 44, which is a key parameter describing the oxidation state of organic aerosol. Following this first major intercomparison exercise of a large number of ACSMs, detailed intercomparison results are presented as well as a discussion of some recommendations about best calibration practices, standardized data processing and data treatment.
Published: 2015

26. Two years of near real-time chemical composition of submicron aerosols in the region of Paris using an Aerosol Chemical Speciation Monitor (ACSm) and a multi-wavelength Aethalometer

Author: Roland Sarda-Esteve, Martial Haeffelin, Olivier Favez, Eva Leoz-Garziandia, Jean Sciare, Nicolas Bonnaire, Vincent Crenn, Jean-Charles Dupont, Jean-Eudes Petit, Griša Močnik, Institut National de l'Environnement Industriel et des Risques (INERIS), Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Chimie Atmosphérique Expérimentale (CAE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Aerosol D.O.O, Laboratoire de Météorologie Dynamique (UMR 8539) (LMD), Département des Géosciences - ENS Paris, École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS)-École des Ponts ParisTech (ENPC)-École polytechnique (X)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut national des sciences de l'Univers (INSU - CNRS)-École polytechnique (X)-École des Ponts ParisTech (ENPC)-Centre National de la Recherche Scientifique (CNRS)-Département des Géosciences - ENS Paris, École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-École normale supérieure - Paris (ENS-PSL), and Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)
Subjects: Pollution, Atmospheric Science, Ammonium sulfate, 010504 meteorology & atmospheric sciences, media_common.quotation_subject, Real-time computing, 010501 environmental sciences, Aethalometer, Combustion, 01 natural sciences, lcsh:QC1-999, Aerosol, lcsh:Chemistry, chemistry.chemical_compound, chemistry, Nitrate, lcsh:QD1-999, 13. Climate action, [SDE]Environmental Sciences, Environmental science, Sulfate, Chemical composition, lcsh:Physics, media_common, 0105 earth and related environmental sciences
Abstract: Aerosol mass spectrometer (AMS) measurements have been successfully used towards a better understanding of non-refractory submicron (PM1) aerosol chemical properties based on short-term campaigns. The recently developed Aerosol Chemical Speciation Monitor (ACSM) has been designed to deliver quite similar artifact-free chemical information but for low cost, and to perform robust monitoring over long-term periods. When deployed in parallel with real-time black carbon (BC) measurements, the combined data set allows for a quasi-comprehensive description of the whole PM1 fraction in near real time. Here we present 2-year long ACSM and BC data sets, between mid-2011 and mid-2013, obtained at the French atmospheric SIRTA supersite that is representative of background PM levels of the region of Paris. This large data set shows intense and time-limited (a few hours) pollution events observed during wintertime in the region of Paris, pointing to local carbonaceous emissions (mainly combustion sources). A non-parametric wind regression analysis was performed on this 2-year data set for the major PM1 constituents (organic matter, nitrate, sulfate and source apportioned BC) and ammonia in order to better refine their geographical origins and assess local/regional/advected contributions whose information is mandatory for efficient mitigation strategies. While ammonium sulfate typically shows a clear advected pattern, ammonium nitrate partially displays a similar feature, but, less expectedly, it also exhibits a significant contribution of regional and local emissions. The contribution of regional background organic aerosols (OA) is significant in spring and summer, while a more pronounced local origin is evidenced during wintertime, whose pattern is also observed for BC originating from domestic wood burning. Using time-resolved ACSM and BC information, seasonally differentiated weekly diurnal profiles of these constituents were investigated and helped to identify the main parameters controlling their temporal variations (sources, meteorological parameters). Finally, a careful investigation of all the major pollution episodes observed over the region of Paris between 2011 and 2013 was performed and classified in terms of chemical composition and the BC-to-sulfate ratio used here as a proxy of the local/regional/advected contribution of PM. In conclusion, these first 2-year quality-controlled measurements of ACSM clearly demonstrate their great potential to monitor on a long-term basis aerosol sources and their geographical origin and provide strategic information in near real time during pollution episodes. They also support the capacity of the ACSM to be proposed as a robust and credible alternative to filter-based sampling techniques for long-term monitoring strategies.
Published: 2014

27. Atmospheric measurements of ratios between CO2 and co-emitted species from traffic: a tunnel study in the Paris megacity

Author: Jean-Eudes Petit, Irène Xueref-Remy, Olivier Perrussel, L. Ammoura, Jean Sciare, Bernard Bonsang, Nicolas Bonnaire, Alexia Baudic, Frédéric Chevallier, and Valérie Gros
Subjects: Atmospheric Science, chemistry.chemical_compound, Atmospheric measurements, Megacity, Acetylene, chemistry, Meteorology, 13. Climate action, Environmental science, Mole fraction, Atmospheric sciences, Benzene, NOx
Abstract: Measurements of CO2, CO, NOx and selected Volatile Organic Compounds (VOCs) mole fractions were performed continuously during a 10-day period in the Guy Môquet tunnel in Thiais, a peri-urban area about 15 km south of the centre of Paris, between 28 September and 8 October 2012. This data set is used here to identify the characteristics of traffic-emitted CO2 by evaluating its ratios to co-emitted species for the first time in the Paris region. High coefficients of determination (r2 > 0.7) are observed between CO2 and certain compounds that are characteristic of the traffic source (CO, NOx, benzene, xylenes and acetylene). Weak correlations (r2 < 0.2) are found with species such as propane, n-butane and i-butane that are associated with fuel evaporation, an insignificant source for CO2. To better characterise the traffic signal we focus only on species that are well-correlated with CO2 and on rush-hour periods characterised by the highest traffic-related mole fractions. From those mole fractions we remove the nighttime-average weekday mole fraction obtained for each species that we infer to be the most appropriate background signal for our study. Then we calculate observed Δspecies / ΔCO2 ratios, which we compare with the ones provided by the 2010 bottom–up high-resolved regional emission inventory from Airparif (the association in charge of monitoring the air quality in Île-de-France), focusing on local emission data for the specific road of the tunnel. We find an excellent agreement (2%) between the local inventory emission CO / CO2 ratio and our observed ΔCO / ΔCO2 ratio. Former tunnel experiments carried out elsewhere in the world provided observed ΔCO / ΔCO2 ratios that differ from 49 to 592% to ours. This variability can be related to technological improvement of vehicles, differences in driving conditions, and fleet composition. We also find a satisfactory agreement with the Airparif inventory for n-propylbenzene, n-pentane and xylenes to CO2 ratios. For most of the other species, the ratios obtained from the local emission inventory overestimate the observed ratios to CO2 by 34 to more than 300%. However, the emission ratios of NOx, o-xylene and i-pentane are underestimated by 30 to 79%. One main cause of such high differences between the inventory and our observations is likely the obsolete feature of the VOCs speciation matrix of the inventory that has not been updated since 1998, although law regulations on some VOCs have occurred since that time. Our study bears important consequences, discussed in the conclusion, for the characterisation of the urban CO2 plume and for atmospheric inverse modelling of urban CO2 emissions.
Published: 2014

28. Sources and geographical origins of fine aerosols in Paris (France)

Author: Jean Sciare, Sophie Moukhtar, E. Poulakis, Véronique Ghersi, José Nicolas, Nicolas Bonnaire, Jean-Eudes Petit, Nikos Mihalopoulos, M. Bressi, Amandine Rosso, C. Theodosi, Anais Feron, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Agence de l'Environnement et de la Maîtrise de l'Energie (ADEME), Chimie Atmosphérique Expérimentale (CAE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), AIRPARIF - Surveillance de la qualité de l'air en Île-de-France, Institut National de l'Environnement Industriel et des Risques (INERIS), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), and Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)
Subjects: Pollution, Atmospheric Science, 010504 meteorology & atmospheric sciences, Meteorology, media_common.quotation_subject, 010501 environmental sciences, 01 natural sciences, lcsh:Chemistry, Urban background, 11. Sustainability, Potential source, Biomass burning, Road traffic, 0105 earth and related environmental sciences, media_common, geography, geography.geographical_feature_category, Contribution function, Local scale, lcsh:QC1-999, lcsh:QD1-999, 13. Climate action, [SDE]Environmental Sciences, Environmental science, Physical geography, lcsh:Physics, Channel (geography)
Abstract: The present study aims at identifying and apportioning fine aerosols to their major sources in Paris (France) – the second most populated "larger urban zone" in Europe – and determining their geographical origins. It is based on the daily chemical composition of PM2.5 examined over 1 year at an urban background site of Paris (Bressi et al., 2013). Positive matrix factorization (EPA PMF3.0) was used to identify and apportion fine aerosols to their sources; bootstrapping was performed to determine the adequate number of PMF factors, and statistics (root mean square error, coefficient of determination, etc.) were examined to better model PM2.5 mass and chemical components. Potential source contribution function (PSCF) and conditional probability function (CPF) allowed the geographical origins of the sources to be assessed; special attention was paid to implement suitable weighting functions. Seven factors, namely ammonium sulfate (A.S.)-rich factor, ammonium nitrate (A.N.)-rich factor, heavy oil combustion, road traffic, biomass burning, marine aerosols and metal industry, were identified; a detailed discussion of their chemical characteristics is reported. They contribute 27, 24, 17, 14, 12, 6 and 1% of PM2.5 mass (14.7 μg m−3) respectively on the annual average; their seasonal variability is discussed. The A.S.- and A.N.-rich factors have undergone mid- or long-range transport from continental Europe; heavy oil combustion mainly stems from northern France and the English Channel, whereas road traffic and biomass burning are primarily locally emitted. Therefore, on average more than half of PM2.5 mass measured in the city of Paris is due to mid- or long-range transport of secondary aerosols stemming from continental Europe, whereas local sources only contribute a quarter of the annual averaged mass. These results imply that fine-aerosol abatement policies conducted at the local scale may not be sufficient to notably reduce PM2.5 levels at urban background sites in Paris, suggesting instead more coordinated strategies amongst neighbouring countries. Similar conclusions might be drawn in other continental urban background sites given the transboundary nature of PM2.5 pollution.
Published: 2014

29. A one-year comprehensive chemical characterisation of fine aerosol (PM2.5) at urban, suburban and rural background sites in the region of Paris (France)

Author: Jean-Eudes Petit, Amandine Rosso, Nikos Mihalopoulos, José Nicolas, Sophie Moukhtar, M. Bressi, Jean Sciare, Nicolas Bonnaire, Anais Feron, Véronique Ghersi, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Agence de l'Environnement et de la Maîtrise de l'Energie (ADEME), Chimie Atmosphérique Expérimentale (CAE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), AIRPARIF - Surveillance de la qualité de l'air en Île-de-France, Environmental Chemical Processes Laboratory [Heraklion] (ECPL), Department of Chemistry [Heraklion], University of Crete [Heraklion] (UOC)-University of Crete [Heraklion] (UOC), The publication of this article is financed by CNRS-INSU., Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), and Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)
Subjects: Pollution, Atmospheric Science, food.ingredient, Meteorology, 010504 meteorology & atmospheric sciences, media_common.quotation_subject, Mineral dust, 010501 environmental sciences, 01 natural sciences, chemistry.chemical_compound, food, Nitrate, 11. Sustainability, Organic matter, Chemical composition, media_common, 0105 earth and related environmental sciences, chemistry.chemical_classification, Total organic carbon, [PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph], Sea salt, Aerosol, chemistry, 13. Climate action, [SDE]Environmental Sciences, Environmental science, Physical geography
Abstract: Studies describing the chemical composition of fine aerosol (PM2.5) in urban areas are often conducted during few weeks only, and at one sole site, giving thus a narrow view of their temporal and spatial characteristics. This paper presents a one-year (11 September 2009–10 September 2010) survey of the daily chemical composition of PM2.5 in the region of Paris, which is the second most populated "Larger Urban Zone" in Europe. Five sampling sites representative of suburban (SUB), urban (URB), northeast (NER), northwest (NWR) and south (SOR) rural backgrounds were implemented. The major chemical components of PM2.5 were determined including elemental carbon (EC), organic carbon (OC), and the major ions. OC was converted to organic matter (OM) using the chemical mass closure methodology, which leads to conversion factors of 1.95 for the SUB and URB sites, and 2.05 for the three rural ones. On average, gravimetrically determined PM2.5 annual mass concentrations are 15.2, 14.8, 12.6, 11.7 and 10.8 μg m−3 for SUB, URB, NER, NWR and SOR sites, respectively. The chemical composition of fine aerosol is very homogeneous at the five sites and is composed of OM (38–47%), nitrate (17–22%), non-sea-salt sulfate (13–16%), ammonium (10–12%), EC (4–10%), mineral dust (2–5%) and sea salt (3–4%). This chemical composition is in agreement with those reported in the literature for most European environments. On the annual scale, Paris (URB and SUB sites) exhibits its highest PM2.5 concentrations during late autumn, winter and early spring (higher than 15 μg m−3 on average, from December to April), intermediates during late spring and early autumn (between 10 and 15 μg m−3 during May, June, September, October, and November) and the lowest during summer (below 10 μg m−3 during July and August). PM levels are mostly homogeneous at the regional scale, on the whole duration of the project (e.g. for URB plotted against NER sites: slope = 1.06, r2 = 0.84, n = 330), suggesting the importance of mid- or long-range transport, and regional instead of local scale phenomena. During this one-year project, two third of the days exceeding the PM2.5 2015 EU annual limit value of 25 μg m−3 were due to continental import from countries located northeast, east of France. This result questions the efficiency of local, regional and even national abatement strategies during pollution episodes, pointing the need for a wider collaborative work with the neighbourhood countries on these topics. Nevertheless, emissions of local anthropogenic sources lead to higher levels at the URB and SUB sites compared to the others (e.g. 26% higher on average at the URB than at the NWR site for PM2.5, during the whole campaign), which can even be emphasised by specific meteorological conditions such as low boundary layer heights. OM and secondary inorganic species (nitrate, non-sea-salt sulfate and ammonium, noted SIA) are mainly imported by mid- or long-range transport (e.g. for NWR plotted against URB sites: slope = 0.79, r2 = 0.72, n = 335 for OM, and slope = 0.91, r2 = 0.89, n = 335 for SIA) whereas EC is primarily locally emitted (e.g. for SOR plotted against URB sites: slope = 0.27; r2 = 0.03; n = 335). This database will serve deepest investigations of carbonaceous aerosols, metals as well as the main sources and geographical origins of PM in the region of Paris.
Published: 2013

30. Étude des composés organiques volatils biogéniques émis par une forêt méditerranéenne

Author: Christophe Boissard, Athina-Cerise Kalogridis, Dominique Baisnée, Elena Ormeño, Nicolas Bonnaire, Anne-Cyrielle Genard, J. Lathière, Roland Sarda-Esteve, Valérie Gros, Catherine Fernandez, Bernard Bonsang, Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Chimie Atmosphérique Expérimentale (CAE), Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Institut méditerranéen de biodiversité et d'écologie marine et continentale (IMBE), Centre National de la Recherche Scientifique (CNRS)-Institut de recherche pour le développement [IRD] : UMR237-Aix Marseille Université (AMU)-Avignon Université (AU), and Modelling the Earth Response to Multiple Anthropogenic Interactions and Dynamics (MERMAID)
Subjects: [PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph], 010504 meteorology & atmospheric sciences, 13. Climate action, 15. Life on land, 010501 environmental sciences, 01 natural sciences, 0105 earth and related environmental sciences
Abstract: International audience; Volatile organic compounds (VOCs) are key components in atmospheric chemistry. On a global scale, biogenic VOCs (BVOCs) constitute approximately 90 % of global VOC emissions. They participate in photochemical reactions and thus play a major role in the formation of tropospheric ozone and secondary organic aerosols. However, the impact of BVOCs on air quality is still characterized by large uncertainties, partly because emissions are not well quantified. As part of the Canopee project, a field campaign took place at the Oak Observatory of the Observatoire de Haute-Provence (O3HP), with the aim of quantifying BVOC emissions from a forest representative of the Mediterranean region.Measurements of concentrations and emission fluxes were carried out from the branch to the canopy level. Branch-level measurements enabled a better understanding of the environmental and physiological parameters of the plant that govern emissions. Fluxmeasurements above the top of the canopy enabled us to quantify the outgoing flow of BVOCs from the forest entering the troposphere. The results showed that white oak is a strong emitter of isoprene but a weak emitter ofmethanol andmonoterpenes. Isoprene emission fluxes were estimated at 7.2 mg m-2 h-1 (under standard conditions of temperature and solar radiation), thusmaking theO3HP forest one of the strongest isoprene emitting ecosystems worldwide; Les composés organiques volatils (COV) sont des composants clés en chimie atmosphérique. À l'échelle globale, on estime que 10 % ont une origine anthropique et 90 % une origine biogénique. L'impact des COV biogéniques (COVB), notamment sur la formation d'ozone (polluant et gaz à effet de serre) et d'aérosols organiques secondaires (à impact sanitaire et radiatif) en font un objet d'étude d'actualité. Toutefois, l'importance de l'impact des COVB sur la qualité de l'air est encore marquée par de larges incertitudes, en partie parce que les émissions demeurent mal quantifiées. Dans le cadre du projet Canopee, une campagne de mesure a eu lieu à l'O3HP, Observatoire du chêne pubescent à l'OHP (Observatoire de Haute-Provence), avec pour objectif de quantifier les émissions de COVB issues d'une forêt représentative de la région méditerranéenne. Des mesures de concentrations et de flux d'émission ont été réalisées à plusieurs échelles : de la branche à la canopée. L'étude des émissions à l'échelle du de la plante a permis une meilleure compréhension des paramètres environnementaux et physiologiques qui régissent les émissions. Les flux de COVB sortant de la canopée et exportés vers la troposphère ont pu être quantifiés. Les résultats montrent que le chêne blanc est un fort émetteur d'isoprène, mais un faible émetteur de méthanol et de monoterpènes. À l'échelle de la forêt, les flux d'émissions d'isoprène ont été estimés à 7,2 mg m-2 h-1 en conditions standard, ce qui fait de l'O3HP un des écosystèmes les plus fortement émetteurs d'isoprène à travers le monde.
Published: 2016

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

Author: Olivier Favez, Cécile Gaimoz, Cristina Dolgorouky, Roland Sarda-Esteve, Valérie Gros, Odile d'Argouges, Bernard Bonsang, Nicolas Bonnaire, and Jean Sciare
Subjects: Atmospheric Science, 010504 meteorology & atmospheric sciences, Soil Science, 010501 environmental sciences, Aquatic Science, Water insoluble, Oceanography, Aethalometer, 01 natural sciences, 7. Clean energy, chemistry.chemical_compound, Geochemistry and Petrology, Earth and Planetary Sciences (miscellaneous), 0105 earth and related environmental sciences, Earth-Surface Processes, Water Science and Technology, Total organic carbon, Ecology, business.industry, Secondary organic aerosols, Levoglucosan, Fossil fuel, Paleontology, Forestry, Aerosol, Geophysics, chemistry, 13. Climate action, Space and Planetary Science, Environmental chemistry, Environmental science, Methanol, business
Abstract: Near 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.
Published: 2011

32. Personal Exposure to Black Carbon, Particulate Matter and Nitrogen Dioxide in the Paris Region Measured by Portable Sensors Worn by Volunteers.

Author: Languille B, Gros V, Nicolas B, Honoré C, Kaufmann A, and Zeitouni K
Abstract: Portable sensors have emerged as a promising solution for personal exposure (PE) measurement. For the first time in Île-de-France, PE to black carbon (BC), particulate matter (PM), and nitrogen dioxide (NO 2 ) was quantified based on three field campaigns involving 37 volunteers from the general public wearing the sensors all day long for a week. This successful deployment demonstrated its ability to quantify PE on a large scale, in various environments (from dense urban to suburban, indoor and outdoor) and in all seasons. The impact of the visited environments was investigated. The proximity to road traffic (for BC and NO 2 ), as well as cooking activities and tobacco smoke (for PM), made significant contributions to total exposure (up to 34%, 26%, and 44%, respectively), even though the time spent in these environments was short. Finally, even if ambient outdoor levels played a role in PE, the prominent impact of the different environments suggests that traditional ambient monitoring stations is not a proper surrogate for PE quantification.
Published: 2022
Full Text: View/download PDF

Catalog

Books, media, physical & digital resources

See catalog results

Searchworks

Select search scope, currently: Articles

Catalog

books, media & more in Jio Institute collections

Articles

journal articles & other e-resources

Refine your results

32 results on '"Nicolas Bonnaire"'

1. NO2, BC and PM Exposure of Participants in the Polluscope Autumn 2019 Campaign in the Paris Region

2. Overview of the French Operational Network for In Situ Observation of PM Chemical Composition and Sources in Urban Environments (CARA Program)

3. Sources and Geographical Origins of PM10 in Metz (France) Using Oxalate as a Marker of Secondary Organic Aerosols by Positive Matrix Factorization Analysis

4. Personal Exposure to Black Carbon, Particulate Matter and Nitrogen Dioxide in the Paris Region Measured by Portable Sensors Worn by Volunteers

5. Detecting and Characterizing Particulate Organic Nitrates with an Aerodyne Long-ToF Aerosol Mass Spectrometer

6. Analysis and determination of secondary organic aerosol (SOA) tracers (markers) in particulate matter standard reference material (SRM 1649b, urban dust)

7. Supplementary material to 'Response of atmospheric composition to COVID-19 lockdown measures during Spring in the Paris region (France)'

8. Response of atmospheric composition to COVID-19 lockdown measures during Spring in the Paris region (France)

9. One-year measurements of secondary organic aerosol (SOA) markers in the Paris region (France): Concentrations, gas/particle partitioning and SOA source apportionment

10. Overview of the French Operational Network for In Situ Observation of PM Chemical Composition and Sources in Urban Environments (CARA Program)

11. A methodology for the characterization of portable sensors for air quality measure with the goal of deployment in citizen science

12. Characterization of particulate and gaseous pollutants from a French dairy and sheep farm

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

14. Sources and Geographical Origins of PM10 in Metz (France) Using Oxalate as a Marker of Secondary Organic Aerosols by Positive Matrix Factorization Analysis

15. Supplementary material to 'Six-year source apportionment of submicron organic aerosols from near-continuous measurements at SIRTA (Paris area, France)'

16. The second ACTRIS inter-comparison (2016) for Aerosol Chemical Speciation Monitors (ACSM): Calibration protocols and instrument performance evaluations

17. Speciation of organic fractions does matter for aerosol source apportionment. Part 3: Combining off-line and on-line measurements

18. ACTRIS ACSM intercomparison – Part 1: Reproducibility of concentration and fragment results from 13 individual Quadrupole Aerosol Chemical Speciation Monitors (Q-ACSM) and consistency with co-located instruments

19. Speciation of organic fractions does matter for aerosol source apportionment. Part 2 : Intensive short-term campaign in the Paris area (France)

20. Organic carbon at a remote site of the western Mediterranean Basin: composition, sources and chemistry during the ChArMEx SOP2 field experiment

21. Supplementary material to 'Organic carbon at a remote site of the western Mediterranean Basin: composition, sources and chemistry during the ChArMEx SOP2 field experiment'

22. Multi-tracer approach to characterize domestic wood burning in Athens (Greece) during wintertime

23. A top-down approach of surface carbonyl sulfide exchange by a Mediterranean oak forest ecosystem in Southern France

24. Initial studies into the characterisation of ripening stages of Emmental cheeses by mid-infrared spectroscopy

26. Two years of near real-time chemical composition of submicron aerosols in the region of Paris using an Aerosol Chemical Speciation Monitor (ACSm) and a multi-wavelength Aethalometer

27. Atmospheric measurements of ratios between CO2 and co-emitted species from traffic: a tunnel study in the Paris megacity

28. Sources and geographical origins of fine aerosols in Paris (France)

29. A one-year comprehensive chemical characterisation of fine aerosol (PM2.5) at urban, suburban and rural background sites in the region of Paris (France)

30. Étude des composés organiques volatils biogéniques émis par une forêt méditerranéenne

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

32. Personal Exposure to Black Carbon, Particulate Matter and Nitrogen Dioxide in the Paris Region Measured by Portable Sensors Worn by Volunteers.

Catalog

Searchworks

Select search scope, currently: Articles Catalog books, media & more in Jio Institute collections Articles journal articles & other e-resources

Search

Search Constraints

Refine your results

Search Limiters

Topic

Publication Year Range

Language

Publication Type

Journal

Database

Publisher

32 results on '"Nicolas Bonnaire"'

Search Results

Catalog

Select search scope, currently: Articles

Catalog

books, media & more in Jio Institute collections

Articles

journal articles & other e-resources