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Size-resolved characteristics of inorganic ionic species in atmospheric aerosols at a regional background site on the South African Highveld North-West University’s research published in Journal of Atmospheric Chemistry. (Research brief)

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CLEAN AIR JOURNAL

15

Volume 28, No 2, 2018

Research brief

Size-resolved characteristics of inorganic ionic

species in atmospheric aerosols at a regional

background site on the South African Highveld

North-West University’s research published in

Journal of Atmospheric Chemistry

Atmospheric aerosols or particulate matter (PM) are important components of the atmosphere with high temporal and spatial variability, which can have significant impacts on air quality and climate change. Detailed physical and chemical characterisation are crucial in establishing the impacts of atmospheric aerosol. Aerosols consist of organic and inorganic species, and the composition and concentration of these species depends on their sources, chemical transformation and sinks. In this study an assessment of major inorganic ions determined in three aerosol particle size ranges, i.e. PM1, PM1-2.5 and PM2.5-10 collected for one year at Welgegund was conducted.

Sulphate (SO42-) and ammonium (NH

4+) dominated the PM1

size fraction, while SO42- and nitrate (NO

3-) dominated the PM 1-2.5 and PM2.5-10 size fractions. SO42- had the highest contribution

in the two smaller size fractions, while NO3- had the highest

contribution in the PM2.5-10 size fraction. SO42- and NO 3- levels

were attributed to the impacts of aged air masses passing over major anthropogenic source regions. Comparison of inorganic ion concentrations to levels thereof within the western Bushveld Igneous Complexes – a source region influencing Welgegund – indicated higher levels of most inorganic species within the source region. However, the comparative ratio of SO42- was

significantly lower due to SO42- being formed distant from SO 2

emissions and submicron SO42- having longer atmospheric

residencies. Aerosols at Welgegund were determined to be generally acidic, which was mainly attributed to high concentrations of SO42-.

PM1 and PM1-2.5 fractions revealed a seasonal pattern, with higher inorganic ion concentrations measured from May to September. Higher PM concentrations were attributed to decreased wet removal, more pronounced inversion layers trapping

Andrew D. Venter

1

, Pieter G. van Zyl

1,

Johan P. Beukes

1

, Jan-Stefan Swartz

1

, Miroslav Josipovic

1

,

Ville Vakkari

2

, Lauri Laakso

1,2

and Markku Kulmala

3

1Unit for Environmental Sciences and Management, North-West University, Potchefstroom, South Africa 2Finnish Meteorological Institute, Helsinki, Finland

3Department of Physics, University of Helsinki, Finland

http://dx.doi.org/10.17159/2410-972X/2018/v28n2a8

pollutants, and increases in household combustion and wild fires during winter. Back trajectory analysis also revealed higher concentrations of inorganic ionic species corresponding to air mass movements over significant anthropogenic activities.

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