Abstract

Abstract. Ground-based measurements of black carbon (BC) were performed near an industrial source region in the early summer of 2014 and at a remote island in Japan in the spring of 2015. Here, we report the temporal variations in the transport, size distributions, and mixing states of the BC-containing particles. These particles were characterized using a continuous soot monitoring system, a single particle soot photometer, and an aerosol chemical speciation monitor. The effects of aging on the growth of BC-containing particles were examined by comparing the ground-based observations between the near-source and remote island sites. Secondary formation of sulfate and organic aerosols strongly affected the increases in BC coating (i.e., enhancement of cloud condensation nuclei activity) with air mass aging from the source to the outflow regions. The effects of wet removal on BC microphysics were elucidated by classifying the continental outflow air masses depending on the enhancement ratios of BC to CO (ΔBC ∕ ΔCO), which were used as an indicator of the transport efficiency of BC. It was found that ΔBC ∕ ΔCO ratios were controlled mainly by the wet removal during transport in the planetary boundary layer (PBL) on the timescale of 1–2 days. The meteorological conditions and backward trajectory analyses suggested that air masses strongly affected by wet removal originated mainly from a region in southern China (20–35° N) in the spring of 2015. Removal of large and thickly coated BC-containing particles was detected in the air masses that were substantially affected by the wet removal in the PBL, as predicted by Köhler theory. The size and water solubility of BC-containing particles in the PBL can be altered by the wet removal as well as the condensation of non-BC materials.

Highlights

  • Black carbon (BC)-containing particles in the atmosphere can significantly affect the radiative budget of the Earth through two effects: direct and indirect effects (Bond et al, 2013; references therein)

  • The subtropical region (20– 30◦ N, 110–130◦ E) was under the influence of a persistent southwesterly flow, part of which was converging into the observation area (30–35◦ N), and this flow was confluent with the northwesterlies from the continent

  • We have reported the temporal variations in the transport and the microphysics of the black carbon (BC)-containing particles, measured using continuous soot-monitoring system (COSMOS), SP2, and aerosol chemical speciation monitor (ACSM)

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Summary

Introduction

Black carbon (BC)-containing particles in the atmosphere can significantly affect the radiative budget of the Earth through two effects: direct (light absorption and scattering) and indirect (aerosol–cloud interactions) effects (Bond et al, 2013; references therein). The difficulty in the estimation of these effects in the atmosphere results from both the short lifetime relative to other greenhouse gases and the variable physicochemical properties of BC-containing particles. The BC itself is water-insoluble immediately after emission, but it subsequently exhibits increased hygroscopicity (McMeeking et al, 2011) and cloud condensation nuclei (CCN) activity (Kuwata et al, 2007) through atmospheric transport and aging. Small amounts of water-soluble materials on BC particles are needed to cause their activation to form cloud droplets under moderate supersaturation conditions It is considered that BC-containing particles are removed from the atmosphere mainly by wet deposition (Seinfeld and Pandis, 2006)

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