Title of article :
Chemical composition, mass size distribution and source analysis
of long-range transported wildfire smokes in Helsinki
Author/Authors :
Markus Sillanp77a، نويسنده , , T، نويسنده , , Sanna Saarikoskia، نويسنده , , Risto Hillamoa، نويسنده , , Arto Pennanenb، نويسنده , ,
Ulla Makkonena، نويسنده , , Zoya Spolnikc، نويسنده , , Rene´ Van Griekenc، نويسنده , ,
Tarja Koskentalod، نويسنده , , Raimo O. Salonenb، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2005
Abstract :
Special episodes of long-range transported particulate (PM) air pollution were investigated in a one-month field campaign at
an urban background site in Helsinki, Finland. A total of nine size-segregated PM samplings of 3- or 4-day duration were made
between August 23 and September 23, 2002. During this warm and unusually dry period there were two (labelled P2 and P5)
sampling periods when the PM2.5 mass concentration increased remarkably. According to the hourly-measured PM data and
backward air mass trajectories, P2 (Aug 23–26) represented a single, 64-h episode of long-range transported aerosol, whereas
P5 (Sept 5–9) was a mixture of two 16- and 14-h episodes and usual seasonal air quality. The large chemical data set, based on
analyses made by ion chromatography, inductively coupled plasma mass spectrometry, X-ray fluorescence analysis and smoke
stain reflectometry, demonstrated that the PM2.5 mass concentrations of biomass signatures (i.e. levoglucosan, oxalate and
potassium) and of some other compounds associated with biomass combustion (succinate and malonate) increased remarkably
in P2. Crustal elements (Fe, Al, Ca and Si) and unidentified matter, presumably consisting to a large extent of organic material,
were also increased in P2. The PM2.5 composition in P5 was different from that in P2, as the inorganic secondary aerosols
(NO3
, SO4
2 , NH4+) and many metals reached their highest concentration in this period. The water-soluble fraction of
potassium, lead and manganese increased in both P2 and P5. Mass size distributions (0.035–10 Am) showed that a large
accumulation mode mainly caused the episodically increased PM2.5 concentrations. An interesting observation was that the
episodes had no obvious impact on the Aitken mode. Finally, the strongly increased concentrations of biomass signatures in
accumulation mode proved that the episode in P2 was due to long-range transported biomass combustion aerosol.
Keywords :
mass size distribution , Source analysis , Biomass combustion markers , Long-range transport , Chemical analysis , Wildfire smoke
Journal title :
Science of the Total Environment
Journal title :
Science of the Total Environment