Abstract. Fine particulate matter with aerodynamic diameters ≤2.5 µm (PM2.5) has adverse effects on human health and the atmospheric environment. The estimation of surface PM2.5 concentrations has made intensive use of satellite-derived aerosol products. However, it has been a great challenge to obtain high-quality and high-resolution PM2.5 data from both ground and satellite observations, which is essential to monitor air pollution over small-scale areas such as metropolitan regions. Here, the space–time extremely randomized trees (STET) model was enhanced by integrating updated spatiotemporal information and additional auxiliary data to improve the spatial resolution and overall accuracy of PM2.5 estimates across China. To this end, the newly released Moderate Resolution Imaging Spectroradiometer Multi-Angle Implementation of Atmospheric Correction AOD product, along with meteorological, topographical and land-use data and pollution emissions, was input to the STET model, and daily 1 km PM2.5 maps for 2018 covering mainland China were produced. The STET model performed well, with a high out-of-sample (out-of-station) cross-validation coefficient of determination (R2) of 0.89 (0.88), a low root-mean-square error of 10.33 (10.93) µg m−3, a small mean absolute error of 6.69 (7.15) µg m−3 and a small mean relative error of 21.28 % (23.69 %). In particular, the model captured well the PM2.5 concentrations at both regional and individual site scales. The North China Plain, the Sichuan Basin and Xinjiang Province always featured high PM2.5 pollution levels, especially in winter. The STET model outperformed most models presented in previous related studies, with a strong predictive power (e.g., monthly R2=0.80), which can be used to estimate historical PM2.5 records. More importantly, this study provides a new approach for obtaining high-resolution and high-quality PM2.5 dataset across mainland China (i.e., ChinaHighPM2.5), important for air pollution studies focused on urban areas.

Abstract. Knowledge of aerosol size and composition is important for determining radiative forcing effects of aerosols, identifying aerosol sources and improving aerosol satellite retrieval algorithms. The ability to extrapolate aerosol size and composition, or type, from intensive aerosol optical properties can help expand the current knowledge of spatiotemporal variability in aerosol type globally, particularly where chemical composition measurements do not exist concurrently with optical property measurements. This study uses medians of the scattering Ångström exponent (SAE), absorption Ångström exponent (AAE) and single scattering albedo (SSA) from 24 stations within the NOAA/ESRL Federated Aerosol Monitoring Network to infer aerosol type using previously published aerosol classification schemes.Three methods are implemented to obtain a best estimate of dominant aerosol type at each station using aerosol optical properties. The first method plots station medians into an AAE vs. SAE plot space, so that a unique combination of intensive properties corresponds with an aerosol type. The second typing method expands on the first by introducing a multivariate cluster analysis, which aims to group stations with similar optical characteristics and thus similar dominantPublished by Copernicus Publications on behalf of the European Geosciences Union. L. Schmeisser et al.: Classifying aerosols with optical propertiesaerosol type. The third and final classification method pairs 3-day backward air mass trajectories with median aerosol optical properties to explore the relationship between trajectory origin (proxy for likely aerosol type) and aerosol intensive parameters, while allowing for multiple dominant aerosol types at each station.The three aerosol classification methods have some common, and thus robust, results. In general, estimating dominant aerosol type using optical properties is best suited for site locations with a stable and homogenous aerosol population, particularly continental polluted (carbonaceous aerosol), marine polluted (carbonaceous aerosol mixed with sea salt) and continental dust/biomass sites (dust and carbonaceous aerosol); however, current classification schemes perform poorly when predicting dominant aerosol type at remote marine and Arctic sites and at stations with more complex locations and topography where variable aerosol populations are not well represented by median optical properties. Although the aerosol classification methods presented here provide new ways to reduce ambiguity in typing schemes, there is more work needed to find aerosol typing methods that are useful for a larger range of geographic locations and aerosol populations.

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Abstract. The aerosol liquid water (ALW) content (ALWC), an important component of atmospheric particles, has a significant effect on atmospheric optical properties, visibility and multiphase chemical reactions. In this study, ALWC is determined from aerosol hygroscopic growth factor (GF) and particle number size distribution (PNSD) measurements and is also simulated by ISORROPIA II, a thermodynamic equilibrium model, with measured aerosol chemical composition data taken at an urban site in Beijing from 8 November to 15 December 2017. Rich measurements made during the experiment concerning virtually all aerosol properties allow us not only to derive the ALWC but also to study the contributions by various species for which little has been done in this region. The simulated ALWC including the contribution of organics and the calculated ALWC are highly correlated (coefficient of determination R2=0.92). The ALWC contributed by organics (ALWCOrg) accounts for 30 %±22 % of the total ALWC during the sampling period. These results suggest a significant contribution of organics to ALWC, which is rather different from previous studies that showed negligible contributions by organics. Our results also show that ALWC correlates well with the mass concentrations of sulfate, nitrate, and secondary organic aerosols (SOAs) (R2=0.66, 0.56 and 0.60, respectively). We further noted that accumulation mode particles play a key role in determining ALWC, dominating among all the aerosol modes. ALWC is an exponential function of ambient relative humidity (RH), whose strong diurnal variation influence the diurnal variation of ALWC. However, there is a 3 h lag between the extremes of ALWC and RH values, due to the diurnal variations in PNSD and aerosol chemical composition. Finally, a case study reveals that ALWCOrg plays an important role in the formation of secondary aerosols through multiphase reactions at the initial stage of a heavy-haze episode.