Atmospheric Chemistry and Physics (Aug 2015)
In situ, satellite measurement and model evidence on the dominant regional contribution to fine particulate matter levels in the Paris megacity
- M. Beekmann,
- A. S. H. Prévôt,
- F. Drewnick,
- J. Sciare,
- S. N. Pandis,
- H. A. C. Denier van der Gon,
- M. Crippa,
- F. Freutel,
- L. Poulain,
- V. Ghersi,
- E. Rodriguez,
- S. Beirle,
- P. Zotter,
- S.-L. von der Weiden-Reinmüller,
- M. Bressi,
- C. Fountoukis,
- H. Petetin,
- S. Szidat,
- J. Schneider,
- A. Rosso,
- I. El Haddad,
- A. Megaritis,
- Q. J. Zhang,
- V. Michoud,
- J. G. Slowik,
- S. Moukhtar,
- P. Kolmonen,
- A. Stohl,
- S. Eckhardt,
- A. Borbon,
- V. Gros,
- N. Marchand,
- J. L. Jaffrezo,
- A. Schwarzenboeck,
- A. Colomb,
- A. Wiedensohler,
- S. Borrmann,
- M. Lawrence,
- A. Baklanov,
- U. Baltensperger
Affiliations
- M. Beekmann
- LISA/IPSL, Laboratoire Interuniversitaire des Systèmes Atmosphériques, UMR CNRS 7583, Université Paris Est Créteil (UPEC) et Université Paris Diderot (UPD), Créteil, France
- A. S. H. Prévôt
- Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, PSI, Villigen, Switzerland
- F. Drewnick
- Particle Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- J. Sciare
- Laboratoire des Sciences du Climat et de l'Environnement (LSCE/IPSL), Laboratoire CEA-CNRS-UVSQ, Gif-sur-Yvette, France
- S. N. Pandis
- Institute of Chemical Engineering Sciences (ICEHT), Foundation for Research and Technology Hellas (FORTH), Patra, Greece
- H. A. C. Denier van der Gon
- Department of Climate, Air and Sustainability, TNO, Utrecht, the Netherlands
- M. Crippa
- Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, PSI, Villigen, Switzerland
- F. Freutel
- Particle Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- L. Poulain
- Leibniz Institute for Tropospheric Research, Leipzig, Germany
- V. Ghersi
- AIRPARIF, Agence de Surveillance de la Qualité de l'Air, Paris, France
- E. Rodriguez
- Climate Change Unit, Finnish Meteorological Institute, 00101, Finland
- S. Beirle
- Max Planck Institute for Chemistry, Satellite Group, Mainz, Germany
- P. Zotter
- Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, PSI, Villigen, Switzerland
- S.-L. von der Weiden-Reinmüller
- Particle Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- M. Bressi
- Laboratoire des Sciences du Climat et de l'Environnement (LSCE/IPSL), Laboratoire CEA-CNRS-UVSQ, Gif-sur-Yvette, France
- C. Fountoukis
- Institute of Chemical Engineering Sciences (ICEHT), Foundation for Research and Technology Hellas (FORTH), Patra, Greece
- H. Petetin
- LISA/IPSL, Laboratoire Interuniversitaire des Systèmes Atmosphériques, UMR CNRS 7583, Université Paris Est Créteil (UPEC) et Université Paris Diderot (UPD), Créteil, France
- S. Szidat
- Department of Chemistry and Biochemistry & Oeschger Centre for Climate Change Research, University of Bern, Bern, Switzerland
- J. Schneider
- Particle Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- A. Rosso
- AIRPARIF, Agence de Surveillance de la Qualité de l'Air, Paris, France
- I. El Haddad
- Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, PSI, Villigen, Switzerland
- A. Megaritis
- Institute of Chemical Engineering Sciences (ICEHT), Foundation for Research and Technology Hellas (FORTH), Patra, Greece
- Q. J. Zhang
- LISA/IPSL, Laboratoire Interuniversitaire des Systèmes Atmosphériques, UMR CNRS 7583, Université Paris Est Créteil (UPEC) et Université Paris Diderot (UPD), Créteil, France
- V. Michoud
- LISA/IPSL, Laboratoire Interuniversitaire des Systèmes Atmosphériques, UMR CNRS 7583, Université Paris Est Créteil (UPEC) et Université Paris Diderot (UPD), Créteil, France
- J. G. Slowik
- Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, PSI, Villigen, Switzerland
- S. Moukhtar
- AIRPARIF, Agence de Surveillance de la Qualité de l'Air, Paris, France
- P. Kolmonen
- Climate Change Unit, Finnish Meteorological Institute, 00101, Finland
- A. Stohl
- NILU – Norwegian Institute for Air Research, Kjeller, Norway
- S. Eckhardt
- NILU – Norwegian Institute for Air Research, Kjeller, Norway
- A. Borbon
- LISA/IPSL, Laboratoire Interuniversitaire des Systèmes Atmosphériques, UMR CNRS 7583, Université Paris Est Créteil (UPEC) et Université Paris Diderot (UPD), Créteil, France
- V. Gros
- Laboratoire des Sciences du Climat et de l'Environnement (LSCE/IPSL), Laboratoire CEA-CNRS-UVSQ, Gif-sur-Yvette, France
- N. Marchand
- Laboratoire Chimie Provence, Equipe Instrumentation et Réactivité Atmosphérique (IRA), Université d'Aix-Marseille-CNRS, Marseille, France
- J. L. Jaffrezo
- Laboratoire de Glaciologie et Géophysique de l'Environnement (LGGE), Université Joseph Fourier, CNRS, Grenoble, France
- A. Schwarzenboeck
- Laboratoire de Météorologie Physique (LaMP), Université Blaise Pascal, CNRS, Aubière, France
- A. Colomb
- LISA/IPSL, Laboratoire Interuniversitaire des Systèmes Atmosphériques, UMR CNRS 7583, Université Paris Est Créteil (UPEC) et Université Paris Diderot (UPD), Créteil, France
- A. Wiedensohler
- Leibniz Institute for Tropospheric Research, Leipzig, Germany
- S. Borrmann
- Particle Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- M. Lawrence
- Department of Atmospheric Chemistry, Max Planck Institute for Chemistry, Mainz, Germany
- A. Baklanov
- Danish Meteorological Institute (DMI), Research Department, Copenhagen, Denmark
- U. Baltensperger
- Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, PSI, Villigen, Switzerland
- DOI
- https://doi.org/10.5194/acp-15-9577-2015
- Journal volume & issue
-
Vol. 15,
no. 16
pp. 9577 – 9591
Abstract
A detailed characterization of air quality in the megacity of Paris (France) during two 1-month intensive campaigns and from additional 1-year observations revealed that about 70 % of the urban background fine particulate matter (PM) is transported on average into the megacity from upwind regions. This dominant influence of regional sources was confirmed by in situ measurements during short intensive and longer-term campaigns, aerosol optical depth (AOD) measurements from ENVISAT, and modeling results from PMCAMx and CHIMERE chemistry transport models. While advection of sulfate is well documented for other megacities, there was surprisingly high contribution from long-range transport for both nitrate and organic aerosol. The origin of organic PM was investigated by comprehensive analysis of aerosol mass spectrometer (AMS), radiocarbon and tracer measurements during two intensive campaigns. Primary fossil fuel combustion emissions constituted less than 20 % in winter and 40 % in summer of carbonaceous fine PM, unexpectedly small for a megacity. Cooking activities and, during winter, residential wood burning are the major primary organic PM sources. This analysis suggests that the major part of secondary organic aerosol is of modern origin, i.e., from biogenic precursors and from wood burning. Black carbon concentrations are on the lower end of values encountered in megacities worldwide, but still represent an issue for air quality. These comparatively low air pollution levels are due to a combination of low emissions per inhabitant, flat terrain, and a meteorology that is in general not conducive to local pollution build-up. This revised picture of a megacity only being partially responsible for its own average and peak PM levels has important implications for air pollution regulation policies.