Mass balance of free tropospheric aerosol at the Puy de Dôme (France) in winter

[1] The size-segregated chemical composition of aerosols was investigated during winters 2000 and 2001 at Puy de Dome (1465 m above sea level, France), a site most of the time located in the free troposphere. Aerosols have been sampled using low-pressure cascade impactors (Electrical Low Pressure Impactor (ELPI) and Small Deposition Impactor (SDI) 13 and 12 stages) and analyzed for inorganic (Na+, NH4+, K+, Mg2+, Ca2+, Cl−, NO3−, and SO42−) and organic (HCOO−, CH3COO−, and C2O42−) ions, organic and elemental carbon (OC and EC), insoluble dust, and total mass. Under cloudy conditions, the sampling includes interstitial aerosol as well as the residue of evaporated cloud droplets. Aerosols (and residues of cloud droplets) were sampled in different air masses, which can be classified into three different categories according to their aerosol load and composition: background (BG), anthropogenic (ANT), and specific events (EV) that include advection of Saharan dust and upward transport from the polluted boundary layer to the site. On the basis of the presence or absence of coarse sea-salt particles, a further classification permits us to distinguish air masses that have or have not been exposed to the ocean. A closed mass balance is achieved on submicron ranges (mean departure of 18.5%) for the three main air mass categories, providing a reliable description of main aerosol types in the west European free troposphere. The total aerosol mass at 50% relative humidity is close to 2.7 ± 0.6 μg m−3 in BG, 5.3 ± 1.0 μg m−3 in ANT, and 15 to 22 μg m−3 in EV air masses. The aerosol mass distribution generally exhibits two submicron modes (Acc1 at 0.2 ± 0.1 μm and Acc2 at 0.5 ± 0.2 μm geometric mean diameter (calculated for every impactor stage) and a supermicron mode (2 ± 1 μm). Aerosols exhibit a high degree of external mixing with carbonaceous (EC and OC) and ionic species associated with Acc1 and Acc2. Concentrations of light carboxylates and mineral dust never exceed 4% of the total content of analyzed compounds, except for a Saharan dust event during which the contribution of insoluble dust reaches 26% of the total aerosol mass. Depending on the sampled air mass, bulk water-soluble inorganic species and carbonaceous material account for 25–70% and 15–60% of the total mass, respectively. The OC fraction is higher in air masses with low aerosol load (53%, 32%, and 22% for BG, ANT, and EV, respectively). Conversely, the EC fraction is enhanced from 4% in BG to 10% in ANT and 14% in EV. The inorganic fraction is more abundant in EV (55%) and ANT (60%) than in BG (40%) air masses as a result of enhanced nit .

[1]  J. Putaud,et al.  Size‐dependent scavenging efficiencies of multicomponent atmospheric aerosols in clouds , 2003 .

[2]  M. Legrand,et al.  Seasonally resolved Alpine and Greenland ice core records of anthropogenic HCl emissions over the 20th century , 2002 .

[3]  R. Hillamo,et al.  Two years of continuous aerosol measurements in northern Finland , 2002 .

[4]  U. Lohmann,et al.  A study of internal and external mixing scenarios and its effect on aerosol optical properties and direct radiative forcing , 2002 .

[5]  R. Hillamo,et al.  Measuring the Size Distribution of Atmospheric Organic and Black Carbon Using Impactor Sampling Coupled with Thermal Carbon Analysis: Method Development and Uncertainties , 2002 .

[6]  Martijn Schaap,et al.  Constructing the European aerosol nitrate concentration field from quality analysed data , 2002 .

[7]  M. Legrand,et al.  Sulfate trends in a Col du Dôme (French Alps) ice core: A record of anthropogenic sulfate levels in the European midtroposphere over the twentieth century , 2001 .

[8]  Detlev Sprung,et al.  Chemical characterization of pollution layers over the tropical Indian Ocean: Signatures of emissions from biomass and fossil fuel burning , 2001 .

[9]  A. Kasper-Giebl,et al.  Black carbon (BC) in alpine aerosols and cloud water—concentrations and scavenging efficiencies , 2001 .

[10]  G. Kiss,et al.  Size resolved chemical mass balance of aerosol particles over rural Hungary , 2001 .

[11]  U. Baltensperger,et al.  Study on the Chemical Character of Water Soluble Organic Compounds in Fine Atmospheric Aerosol at the Jungfraujoch , 2001 .

[12]  J. Putaud,et al.  Chemical composition of marine aerosol in a Mediterranean coastal zone during the FETCH experiment , 2001 .

[13]  Barbara J. Turpin,et al.  Species Contributions to PM2.5 Mass Concentrations: Revisiting Common Assumptions for Estimating Organic Mass , 2001 .

[14]  A. Kasper-Giebl,et al.  Black carbon and other species at a high‐elevation European site (Mount Sonnblick, 3106 m, Austria): Concentrations and scavenging efficiencies , 2000 .

[15]  H. Hansson,et al.  Hygroscopic growth of ultrafine ammonium sulphate aerosol measured using an ultrafine tandem differential mobility analyzer , 2000 .

[16]  A. Limbeck,et al.  Dependence of in-cloud scavenging of polar organic aerosol compounds on the water solubility , 2000 .

[17]  N. Mihalopoulos,et al.  Carboxylic acids in gas and particulate phase above the Atlantic Ocean , 2000 .

[18]  H. Hansson,et al.  Organic atmospheric aerosols: Review and state of the science , 2000 .

[19]  M. Legrand,et al.  Scavenging of acidic gases (HCOOH, CH3COOH, HNO3, HCl, and SO2) and ammonia in mixed liquid‐solid water clouds at the Puy de Dôme mountain (France) , 2000 .

[20]  P. J. Rasch,et al.  Sulfur chemistry in the National Center for Atmospheric Research Community Climate Model: Description, evaluation, features, and sensitivity to aqueous chemistry , 2000 .

[21]  D. Covert,et al.  Size-segregated chemical, gravimetric and number distribution-derived mass closure of the aerosol in Sagres, Portugal during ACE-2 , 2000 .

[22]  P. Quinn,et al.  Shipboard measurements of concentrations and properties of carbonaceous aerosols during ACE-2 , 2000 .

[23]  R. Van Dingenen,et al.  Chemical mass closure and assessment of the origin of the submicron aerosol in the marine boundary layer and the free troposphere at Tenerife during ACE-2 , 2000 .

[24]  J. Offenberg,et al.  Aerosol size distributions of elemental and organic carbon in urban and over-water atmospheres , 2000 .

[25]  P. Warneck Chemistry of the natural atmosphere , 1999 .

[26]  U. Baltensperger,et al.  Elemental carbon (EC) and black carbon (BC) measurements with a thermal method and an aethalometer at the high-alpine research station Jungfraujoch , 1999 .

[27]  Hans-Christen Hansson,et al.  Inorganic, organic and macromolecular components of fine aerosol in different areas of Europe in relation to their water solubility , 1999 .

[28]  R. Hillamo,et al.  Size-segregated chemistry of particulate dicarboxylic acids in the Arctic atmosphere , 1999 .

[29]  P. Buseck,et al.  Airborne minerals and related aerosol particles: effects on climate and the environment. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[30]  H. Puxbaum,et al.  Seasonal variation of SO2, HNO3, NH3 and selected aerosol components at Sonnblick (3106 m a.s.l.) , 1998 .

[31]  H. Hansson,et al.  NaCl Aerosol Particle Hygroscopicity Dependence on Mixing with Organic Compounds , 1998 .

[32]  P. Buseck,et al.  Wet and dry sizes of atmospheric aerosol particles: An AFM‐TEM Study , 1998 .

[33]  U. Baltensperger,et al.  The Jungfraujoch high‐alpine research station (3454 m) as a background clean continental site for the measurement of aerosol parameters , 1998 .

[34]  B. Huebert,et al.  A field intercomparison of three cascade impactors , 1998 .

[35]  P. Hobbs,et al.  Airborne measurements of carbonaceous aerosols on the East Coast of the United States , 1997 .

[36]  S. Jennings,et al.  Microphysical and physico-chemical characterization of atmospheric marine and continental aerosol at mace head , 1997 .

[37]  B. Turpin,et al.  Characterization of the Southwestern Desert Aerosol, Meadview, AZ. , 1997, Journal of the Air & Waste Management Association.

[38]  Shui-Jen Chen,et al.  Particle Size Distribution of Aerosol Carbons in Ambient Air , 1997 .

[39]  Judith C. Chow,et al.  Descriptive analysis of PM2.5 and PM10 at regionally representative locations during SJVAQS/AUSPEX , 1996 .

[40]  P. Saxena,et al.  Water-soluble organics in atmospheric particles: A critical review of the literature and application of thermodynamics to identify candidate compounds , 1996 .

[41]  L. Barrie,et al.  Source and reaction pathways of dicarboxylic acids, ketoacids and dicarbonyls in arctic aerosols: One year of observations , 1996 .

[42]  R. Hillamo,et al.  A new cascade impactor for aerosol sampling with subsequent PIXE analysis , 1996 .

[43]  P. Pilewskie,et al.  Vertical profiles, aerosol microphysics, and optical closure during the Atlantic Stratocumulus Transition Experiment: Measured and modeled column optical properties , 1996 .

[44]  B. Huebert,et al.  Sulfate, nitrate, methanesulfonate, chloride, ammonium, and sodium measurements from ship, island, and aircraft during the Atlantic Stratocumulus Transition Experiment/Marine Aerosol Gas Exchange , 1996 .

[45]  D. Wagenbach,et al.  Northward Transport of Saharan Dust Recorded in a Deep Alpine Ice Core , 1996 .

[46]  A. Wexler,et al.  Growth laws for atmospheric aerosol particles: An examination of the bimodality of the accumulation mode , 1995 .

[47]  P. Seibert,et al.  A study of an outstanding Saharan dust event at the high-alpine site Jungfraujoch, Switzerland , 1995 .

[48]  Barbara J. Turpin,et al.  Investigation of organic aerosol sampling artifacts in the los angeles basin , 1994 .

[49]  R. Delmas,et al.  Snow chemistry of high altitude glaciers in the French Alps , 1994 .

[50]  J. Seinfeld,et al.  On the Source of the Submicrometer Droplet Mode of Urban and Regional Aerosols , 1994 .

[51]  T. Nunes,et al.  Carbonaceous aerosols in industrial and coastal atmospheres , 1993 .

[52]  Judith C. Chow,et al.  The dri thermal/optical reflectance carbon analysis system: description, evaluation and applications in U.S. Air quality studies , 1993 .

[53]  D. Covert,et al.  On the distribution of physical and chemical particle properties in the atmospheric aerosol , 1990 .

[54]  Hélène Cachier,et al.  Determination of atmospheric soot carbon with a simple thermal method , 1989 .

[55]  J. Heintzenberg Fine particles in the global troposphere. A review , 1989 .

[56]  M. Desbois,et al.  Present Transport and Deposition Patterns of African Dusts to the North-Western Mediterranean , 1989 .

[57]  J. Huntzicker,et al.  Vapor adsorption artifact in the sampling of organic aerosol: Face velocity effects , 1986 .

[58]  W. Zoller,et al.  Diurnal and longer‐term temporal changes in the composition of atmospheric particles at Mauna Loa, Hawaii , 1984 .

[59]  M. Andreae Soot Carbon and Excess Fine Potassium: Long-Range Transport of Combustion-Derived Aerosols , 1983, Science.

[60]  M. L. Laucks,et al.  Aerosol Technology Properties, Behavior, and Measurement of Airborne Particles , 2000 .

[61]  R. C. Weast CRC Handbook of Chemistry and Physics , 1973 .

[62]  E. D. Cyan Handbook of Chemistry and Physics , 1970 .