Characterization of atmospheric trace gas and aerosol concentrations at forest sites in southern and northern Finland using back trajectories

The trace gas and aerosol concentrations as well as meteorological data (radiation, temperature, humidity) measured in Hyytiälä and Värriö, southern and northern Finland, respectively, were investigated with air mass analyses. The back trajectories of air masses arriving to the sites on the 925-hPa pressure level were calculated 96 hours backwards in time. Two trajectories per day, arriving at 00 UTC and 12 UTC, were computed. The studied time period covered December 1997 to August 1998, November 1998 to July 1999, and September 1999. The arriving air masses were divided into five sectors according to their origin: I = North–West (Arctic Ocean), II = North–East (Northern Russia, Kola Peninsula), III = South–East (Southern Russia, St. Petersburg), IV = South–West (Central Europe, Great Britain), and V Local, circulating air masses. The climatology of various properties of air masses originating from different sectors was studied. The analysis showed differences between typically clean (sectors I and II) and polluted (sectors III and IV) air masses. In air masses from sectors III and IV, the NOx concentrations were high during all seasons, but the O3 concentrations were high during the spring and summer seasons and low in winter. The highest SO2 concentrations arrived from sector III. In Värriö also the air from sector II was accompanied with higher SO2 concentrations and some very high peaks were observed in winter when air masses passed through the industrial area of Kola Peninsula. Nucleation events typically occurred in clean air masses and accumulation mode concentrations were higher in polluted air masses. Although there were some differences between Hyytiälä and Värriö, the overall behaviour was similar at both sites.

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Publication Details

Journal
Boreal Environment Research Journal Archive
Published
2024-12-12
DOI
https://doi.org/10.60910/x81b-zr35
Citations
35
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
2.26
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article

Characterization of atmospheric trace gas and aerosol concentrations at forest sites in southern and northern Finland using back trajectories

Markku Kulmala, Jussi Paatero, Timo Vesala, Ari Asmi et al.
35 citations
Boreal Environment Research Journal Archive
Atmospheric chemistry and aerosols
2.26
article

Characterization of atmospheric trace gas and aerosol concentrations at forest sites in southern and northern Finland using back trajectories

Markku Kulmala, Jussi Paatero, Timo Vesala, Ari Asmi, Arto Puustinen, Üllar Rannik, A. Jäppinen, Janne Karimäki, S. Yli-Koivisto, J. Raittila, Tanja Suni, Miikka Dal Maso, S.-P. Malvikko, Sami Romakkaniemi, Liisa Pirjola, Hannele Korhonen, Veli Karhu
article en
35 citations

Abstract

The trace gas and aerosol concentrations as well as meteorological data (radiation, temperature, humidity) measured in Hyytiälä and Värriö, southern and northern Finland, respectively, were investigated with air mass analyses. The back trajectories of air masses arriving to the sites on the 925-hPa pressure level were calculated 96 hours backwards in time. Two trajectories per day, arriving at 00 UTC and 12 UTC, were computed. The studied time period covered December 1997 to August 1998, November 1998 to July 1999, and September 1999. The arriving air masses were divided into five sectors according to their origin: I = North–West (Arctic Ocean), II = North–East (Northern Russia, Kola Peninsula), III = South–East (Southern Russia, St. Petersburg), IV = South–West (Central Europe, Great Britain), and V Local, circulating air masses. The climatology of various properties of air masses originating from different sectors was studied. The analysis showed differences between typically clean (sectors I and II) and polluted (sectors III and IV) air masses. In air masses from sectors III and IV, the NOx concentrations were high during all seasons, but the O3 concentrations were high during the spring and summer seasons and low in winter. The highest SO2 concentrations arrived from sector III. In Värriö also the air from sector II was accompanied with higher SO2 concentrations and some very high peaks were observed in winter when air masses passed through the industrial area of Kola Peninsula. Nucleation events typically occurred in clean air masses and accumulation mode concentrations were higher in polluted air masses. Although there were some differences between Hyytiälä and Värriö, the overall behaviour was similar at both sites.

Boreal Environment Research Journal Archive
Openalex Percentile: Top 15%
Atmospheric chemistry and aerosols
2.26
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