Abstract

A long- and large-range heavy dust episode occurred from 3 to 8 May 2017 in China. To explore the impacts of this long-range dust transport episode on the chemical compositions and size distributions of urban aerosols, such instruments as an online analyzer for monitoring aerosols and gases (MARGA) and a wide-range particle spectrometer (WPS) were mainly used to monitor chemical components, such as PM2.5 and aerosol size distributions in the range of 10 nm to 10 μm, in Nanjing in this study. During the dust episode, the average concentrations of PM2.5 and PM10 and ions of Ca2+, Mg2+, Cl-, SO42−, NO3−, and NH4+ were 66.2, 233.9, and 1.1, 1.5, 1.1, 11.4, 7.8 and 4.4 μg·m−3, which were 4.4, 5.8, 3.7, 15, 1.38, 1.84, 1.66 and 1.83 times higher than the values observed before the episode and 2.2, 3.3, 5.5, 5.0, 1.57, 1.97, 1.39 and 1.69 times the levels after the episode. The dusts were demonstrated to have differential impacts on the water-soluble gases in the air. During the dust episode, the concentrations of HCl, SO2 and NH3 were comparably low, while the HNO2 and HNO3 concentrations were high. The diurnal variations in pollutants, including SO2, HNO3, Cl−, Ca2+, Mg2+, PM2.5 and PM10, were strongly impacted by the dust episode. However, those variations in NH3, NO3−, SO42− and NH4+ were only slightly influenced. Pollutants were distinctively featured in the various dust stages. The concentration of HNO2 was relatively high in the earliest stage but was substituted by those of SO2, PM10, PM2.5, Ca2+, Mg2+ HNO3 and Cl- in the explosion stage. The aerosol number concentrations exhibited unimodal distributions in the earliest and explosion stages but showed bimodal distributions in the duration and dissipation stages. Additionally, the aerosol size distributions were observed to shift to larger particle segments in different dust stages. The surface area concentrations exhibited four peaks in different dust stages and exhibited trimodal distributions in the non-dust episode. The surface area concentration of fine particles first increased during the earliest stage, while that of coarse particles first decreased during the dissipation stage.

Highlights

  • As one of the major components of atmospheric aerosols, dust aerosols account for 50% of global aerosols [1,2]

  • The surface area concentration of fine particles first increased during the earliest stage, while that of coarse particles first decreased during the dissipation stage

  • Dust storms even occurred in some districts of inner Mongolia

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Summary

Introduction

As one of the major components of atmospheric aerosols, dust aerosols account for 50% of global aerosols [1,2]. Dust aerosols can influence the energy balance of the Earth’s atmosphere by absorbing. Dust aerosols may serve as the reaction interfaces for heterogeneous reactions that further influence atmospheric chemical processes [8,9,10]. Dust aerosols delivered upward can experience long-range transportation and subsequently affect Earth’s biological cycles when the aerosols sink to the ground and the ocean [11,12,13]. East Asia is a major source of dust in the world. The estimates for annual global dust emissions range from 1000 to 3000 trillion grams (Tg), and Asian deserts are assumed to constitute 10–25%

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