Abstract. A severe dust storm event originated from the Gobi Desert in Central and East Asia during 2–7 May 2017. Based on Moderate Resolution Imaging Spectroradiometer (MODIS) satellite products, hourly environmental monitoring measurements from Chinese cities and East Asian meteorological observation stations, and numerical simulations, we analysed the spatial and temporal characteristics of this dust event as well as its associated impact on the Asia-Pacific region. The maximum observed hourly PM10 (particulate matter with an aerodynamic diameter ≤ 10 µm) concentration was above 1000 µg m−3 in Beijing, Tianjin, Shijiazhuang, Baoding, and Langfang and above 2000 µg m−3 in Erdos, Hohhot, Baotou, and Alxa in northern China. This dust event affected over 8.35 million km2, or 87 % of the Chinese mainland, and significantly deteriorated air quality in 316 cities of the 367 cities examined across China. The maximum surface wind speed during the dust storm was 23–24 m s−1 in the Mongolian Gobi Desert and 20–22 m s−1 in central Inner Mongolia, indicating the potential source regions of this dust event. Lidar-derived vertical dust profiles in Beijing, Seoul, and Tokyo indicated dust aerosols were uplifted to an altitude of 1.5–3.5 km, whereas simulations by the Weather Research and Forecasting with Chemistry (WRF-Chem) model indicated 20.4 and 5.3 Tg of aeolian dust being deposited respectively across continental Asia and the North Pacific Ocean. According to forward trajectory analysis by the FLEXible PARTicle dispersion (FLEXPART) model, the East Asian dust plume moved across the North Pacific within a week. Dust concentrations decreased from the East Asian continent across the Pacific Ocean from a magnitude of 103 to 10−5 µg m−3, while dust deposition intensity ranged from 104 to 10−1 mg m−2. This dust event was unusual due to its impact on continental China, the Korean Peninsula, Japan, and the North Pacific Ocean. Asian dust storms such as those observed in early May 2017 may lead to wider climate forcing on a global scale.

Abstract. Black carbon aerosols play an important role in climate change because they directly absorb solar radiation. In this study, the mixing state of refractory black carbon (rBC) at an urban site in Beijing in the early summer of 2018 was studied with a single-particle soot photometer (SP2) as well as a tandem observation system with a centrifugal particle mass analyzer (CPMA) and a differential mobility analyzer (DMA). The results demonstrated that the mass-equivalent size distribution of rBC exhibited an approximately lognormal distribution with a mass median diameter (MMD) of 171 nm. When the site experienced prevailing southerly winds, the MMD of rBC increased notably, by 19 %. During the observational period, the ratio of the diameter of rBC-containing particles (Dp) to the rBC core (Dc) was 1.20 on average for Dc=180 nm, indicating that the majority of rBC particles were thinly coated. The Dp∕Dc value exhibited a clear diurnal pattern, with a maximum at 14:00 LST and a Dp growth rate of 2.3 nm h−1; higher Ox conditions increased the coating growth rate. The microphysical properties of rBC were also studied. Bare rBC particles were mostly found in fractal structures with a mass fractal dimensions (Dfm) of 2.35, with limited variation during both clean and polluted periods. The morphology of rBC changed with coating thickness increasing. When the mass ratio of nonrefractory matter to rBC (MR) was <1.5, rBC-containing particles were primarily found in external fractal structures, and they changed to a core–shell structure when MR>6, at which point the measured scattering cross section of rBC-containing particles was consistent with that based on the Mie-scattering simulation. We found that only 28 % of the rBC-containing particles were in core–shell structures with a particle mass of 10 fg in the clean period but that proportion increased considerably, to 45 %, in the polluted period. Due to the morphology change, the absorption enhancement (Eabs) was 12 % lower than that predicted for core–shell structures.

Depolarization ratio (δ) of backscattered light is an applicable parameter for distinguishing the sphericity of particles in real time, which has been widely adopted by groundbased lidar observation systems. In this study, δ values of particles and chemical compositions in both PM 2.5 (aerodynamic diameter less than 2.5 µm) and PM 10 (aerodynamic diameter less than 10 µm) were concurrently measured on the basis of a bench-top optical particle counter with a polarization detection module (POPC) and a continuous dichotomous aerosol chemical speciation analyzer (ACSA-14) from November 2016 to February 2017 at an urban site in Beijing megacity. In general, measured δ values depended on both size and sphericity of the particles. During the observation period, mass concentrations of NO − 3 in PM 2.5 (f NO 3 ) were about an order of magnitude higher than that in PM 2.5−10 (cNO 3 ) with a mean f NO 3 /cNO 3 ratio of 14 ± 10. A relatively low f NO 3 /cNO 3 ratio (∼ 5) was also observed under higher relative humidity conditions, mostly due to heterogeneous processes and particles in the coarse mode. We found that δ values of ambient particles in both PM 2.5 and PM 2.5−10 obviously decreased as mass concentration of water-soluble species increased at unfavorable meteorological conditions. This indicated that the morphology of particles was changed as a result of water-absorbing processes. The particles with optical size (Dp) of Dp = 5 µm were used to represent mineral dust particles, and its δ values (δ Dp=5 ) decreased by 50 % as the mass fraction of cNO 3 increased from 2 % to 8 % and ambient relative humidity increased up to 80 %, suggesting that mineral dust particles were likely to be spherical during humid pollution episodes. During the observation, relative humidity inside the POPC measuring chamber was stable at 34 ± 2 %, lower than the ambient condition. Its influence on the morphology was estimated to be limited and did not change our major conclusion. This study highlights the evident alteration of non-sphericity of mineral dust particles during their transport owing to a synergistic effect of both pollutant coatings and hygroscopic processes, which plays an important role in the evaluation of its environmental effect.

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