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Volume 13, issue 8
Atmos. Chem. Phys., 13, 4291-4306, 2013
https://doi.org/10.5194/acp-13-4291-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 13, 4291-4306, 2013
https://doi.org/10.5194/acp-13-4291-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 25 Apr 2013

Research article | 25 Apr 2013

Volatile organic compounds in the western Mediterranean basin: urban and rural winter measurements during the DAURE campaign

R. Seco1,2,*, J. Peñuelas1,2, I. Filella1,2, J. Llusia1,2, S. Schallhart3,**, A. Metzger4, M. Müller3, and A. Hansel3 R. Seco et al.
  • 1CREAF, Cerdanyola del Vallès 08193, Catalonia, Spain
  • 2CSIC, Global Ecology Unit CREAF-CEAB-UAB, Cerdanyola del Vallès 08193 Catalonia, Spain
  • 3Institut für Ionenphysik und Angewandte Physik, Universität Innsbruck, Technikerstrasse 25, 6020 Innsbruck, Austria
  • 4Ionicon Analytik, Eduard-Bodemgasse 3, 6020 Innsbruck, Austria
  • *now at: Atmospheric Chemistry Division, National Center for Atmospheric Research, Boulder, CO 80301, USA
  • **now at: Department of Physics, Division of Atmospheric Sciences P.O. Box 64, Gustaf Hällströminkatu 2, 00014 University of Helsinki, Helsinki, Finland

Abstract. Atmospheric volatile organic compounds (VOCs) have key environmental and biological roles, but little is known about the daily VOC mixing ratios in Mediterranean urban and natural environments. We measured VOC mixing ratios concurrently at an urban and a rural site during the winter DAURE campaign in the northeastern Iberian Peninsula, by means of PTR-MS at both locations: a PTR-Quad-MS at the urban site and a PTR-ToF-MS at the rural site. All VOC mixing ratios measured were higher at the urban site (e.g. acetaldehyde, isoprene, benzene, and toluene with averages up to 1.68, 0.31, 0.58 and 2.71 ppbv, respectively), with the exception of some short-chain oxygenated VOCs such as acetone (with similar averages of 0.7–1.6 ppbv at both sites). The average diurnal pattern also differed between the sites. Most of the VOCs at the urban location showed their highest mixing ratios in the morning and evening. These peaks coincided with traffic during rush hour, the main origin of most of the VOCs analyzed. Between these two peaks, the sea breeze transported the urban air inland, thus helping to lower the VOC loading at the urban site. At the rural site, most of the measured VOCs were advected by the midday sea breeze, yielding the highest daily VOC mixing ratios (e.g. acetaldehyde, isoprene, benzene, and toluene with averages up to 0.65, 0.07, 0.19, and 0.41 ppbv, respectively). Only biogenic monoterpenes showed a clear local origin at this site. In addition, the concentrations of fine particulate matter observed at both sites, together with the synoptic meteorological conditions and radio-sounding data, allowed the identification of different atmospheric scenarios that had a clear influence on the measured VOC mixing ratios. These results highlight the differences and relationships in VOC mixing ratios between nearby urban and rural areas in Mediterranean regions. Further research in other urban-rural areas is warranted to better understand the urban-rural influence on atmospheric VOC mixing ratios under different atmospheric conditions.

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