In-depth characterization of submicron particulate matter inter-annual variations at a street canyon site in northern Europe

被引:23
作者
Barreira, Luis M. F. [1 ]
Helin, Aku [1 ]
Aurela, Minna [1 ]
Teinila, Kimmo [1 ]
Friman, Milla [1 ]
Kangas, Leena [1 ]
Niemi, Jarkko, V [2 ]
Portin, Harri [2 ]
Kousa, Anu [2 ]
Pirjola, Liisa [3 ]
Ronkko, Topi [4 ]
Saarikoski, Sanna [1 ]
Timonen, Hilkka [1 ]
机构
[1] Finnish Meteorol Inst, Atmospher Composit Res, Helsinki 00101, Finland
[2] Helsinki Reg Environm Serv Author, Helsinki 00066, Finland
[3] Metropolia Univ Appl Sci, Dept Automot & Mech Engn, Vantaa 01600, Finland
[4] Tampere Univ, Fac Engn & Nat Sci, Phys Unit, Aerosol Phys Lab, Tampere 33014, Finland
基金
芬兰科学院;
关键词
HELSINKI METROPOLITAN-AREA; AEROSOL LIGHT-ABSORPTION; BLACK CARBON; SOURCE APPORTIONMENT; CHEMICAL-COMPOSITION; AIR-QUALITY; AMBIENT MEASUREMENTS; ORGANIC AEROSOLS; TRENDS; HEALTH;
D O I
10.5194/acp-21-6297-2021
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Atmospheric aerosols play an important role in air pollution. Aerosol particle chemical composition is highly variable depending on the season, hour of the day, day of the week, meteorology, and location of the measurement site. Long measurement periods and highly time-resolved data are required in order to achieve a statistically relevant amount of data for assessing those variations and evaluating pollution episodes. In this study, we present continuous atmospheric PM1 (particulate matter < 1 mu m) concentration and composition measurements at an urban street canyon site located in Helsinki, Finland. The study was performed for 4.5 years (2015-2019) and involved highly time-resolved measurements by taking advantage of a suite of online state-of-the-art instruments such as an aerosol chemical speciation monitor (ACSM), a multi-angle absorption photometer (MAAP), a differential mobility particle sizer (DMPS), and an Aethalometer (AE). PM1 consisted mostly of organics, with mean mass concentrations of 2.89 mu g m(-3) (53% of PM1) followed by inorganic species (1.56 mu g m(-3), 29 %) and equivalent black carbon (eBC, 0.97 mu g m(-3), 18 %). A trend analysis revealed a decrease in BC from fossil fuel (BCFF), organics, and nitrate over the studied years. Clear seasonal and/or diurnal variations were found for the measured atmospheric PM1 constituents. Particle number and mass size distributions over different seasons revealed the possible influence of secondary organic aerosols (SOAs) during summer and the dominance of ultrafine traffic aerosols during winter. The seasonality of measured constituents also impacted the particle's coating and absorptive properties. The investigation of pollution episodes observed at the site showed that a large fraction of aerosol particle mass was comprised of inorganic species during long-range transport, while during local episodes eBC and organics prevailed together with elevated particle number concentration. Overall, the results increased knowledge of the variability of PM1 concentration and composition in a Nordic traffic site and its implications on urban air quality. Considering the effects of PM mitigation policies in northern Europe in the last decades, the results obtained in this study may be considered illustrative of probable future air quality challenges in countries currently adopting similar environmental regulations.
引用
收藏
页码:6297 / 6314
页数:18
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