Abstract

In spring 2013 air samples were collected from a coastal site in the sparsely populated far south-west of Taiwan and analysed for ambient gases, inorganic salts, carboxylates, and saccharides. Concentration of ambient gases was in the order SO_2 > HCl > HNO_3 > NH_3 > HNO_2. Day-night variation in concentrations indicated that photochemical conversion of HNO_2 to HNO_3 occurs during the day. PM_(2.5) (16.16 ± 5.30 μg m^(-3)) accounted for 61.1% of PM10 mass concentrations. The main inorganic salts were SO_4 ^(2-), NH_4 ^+, Na^+, NO_3 ^-, and Cl^-, collectively accounting for 48.8 ± 27.4% of the PM_(2.5). Cldepletion during the day was higher than during the night due to the presence of reactive photochemical products. The average Cl-depletion of PM_(2.5) (53.1%) was markedly higher than that of PM_(2.5-10) (26.0%), indicating that in PM_(2.5), a high amount of Cl^- reacts with acidic gases to form HCl, which then escapes into the atmosphere. The carboxylate concentration in PM_(2.5) was 0.50 ± 0.24 μg m^(-3). It was found that low-molecular-weight carboxylates formed more readily in the open coastal region than in urban regions of southern Taiwan. Additionally, the daily mean ratio of Oxalate/non-seasalt SO_4 ^(2-) (6.15 ± 2.28%) in the coastal region was higher than that in the urban regions in southern Taiwan. The most prevalent saccharide in PM_(2.5) was myo-inosital (333 ± 300 μg m^(-3)), a type of soil fungus metabolite. Emissions of arabitol and mannitol, emitted through lichen and fungal activity, were markedly higher during the day. Only a trace amount (8.92 ± 16.92 μg m^(-3)) of Levoglucosan (Levo), an indicator of biomass burning, was detected. The mean Levo/organic carbon ratio was 5.04 ± 8.72‰, suggesting that biomass burning contributed slightly to aerosols in the study area. An analysis of air mass backward trajectories showed that the products of biomass burning in Southeast Asia and southern China may be transported to the study area through long-range transport. This effect is more noticeable during the day when onshore breezes support the transport of particles sourced from the west of Taiwan.

Highlights

  • Marine aerosols, composed mostly of sea salts (Hsu et al, 2007a), can scatter solar radiation and affect the formation of cloud condensation nuclei, thereby influencing regional meteorology and ambient radiation transmissions (Fitzgerald, 1991; Gustafsson and Franzén, 1996; O'Dowd et al, 1997; Vignati et al, 2010)

  • This implies that in the presence of sunlight, the NOx emitted from non-traffic sources in the area undergoes photochemical reaction, causing the conversion of intermediates (HNO2) to HNO3 (Sjödin and Ferm, 1985; Lin and Cheng, 2007), thereby leading low HNO2 and high HNO3 daytime concentrations

  • The results reveal that the three waves of airflows that apparently passed through the concentrated biomass burning areas carried PM2.5 with Levo concentrations of 20.2– 79.4 ng m–3 and a Levo/organic carbon (OC) ratio of 24.5%–30.3‰, which are markedly higher than those measured during our 7week study period (Levo: 8.92 ± 16.92 ng m–3; Levoglucosan/ organic carbon (Levo/OC): 5.04 ± 8.72‰), in which Levo was observed only in the fine PM2.5

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Summary

Introduction

Marine aerosols, composed mostly of sea salts (Hsu et al, 2007a), can scatter solar radiation and affect the formation of cloud condensation nuclei, thereby influencing regional meteorology and ambient radiation transmissions (Fitzgerald, 1991; Gustafsson and Franzén, 1996; O'Dowd et al, 1997; Vignati et al, 2010). Na+ was the third most abundant species, with a concentration higher than that of NO3– illustrating that the composition of aerosols in the coastal region of southern Taiwan differs from that typical in urban areas (Remoundaki et al, 2013).

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