Abstract.A global vertically resolved aerosol data set covering more than 10 years of observations at more than 20 measurement sites distributed from 63 • N to 52 • S and 72 • W to 124 • E has been achieved within the Raman and polarization lidar network Polly NET . This network consists of portable, remote-controlled multiwavelength-polarization-Raman lidars (Polly) for automated and continuous 24/7 observations of clouds and aerosols. Polly NET is an independent, voluntary, and scientific network. All Polly lidars feature a standardized instrument design with different capabilities ranging from single wavelength to multiwavelength systems, and now apply unified calibration, quality control, and data analysis. The observations are processed in near-real time without manual intervention, and are presented online at polly.tropos.de. The paper gives an overview of the observations on four continents and two research vessels obtained with eight Polly systems. The specific aerosol types at these locations (mineral dust, smoke, dust-smoke and other dusty mixtures, urban haze, and volcanic ash) are identified by their Ångström exponent, lidar ratio, and depolarization ratio. The vertical aerosol distribution at the Polly NET locations is discussed on the basis of more than 55 000 automatically retrieved 30 min particle backscatter coefficient profiles at 532 nm as this operating wavelength is available for all Polly lidar systems. A seasonal analysis of measurements at selected sites revealed typical and extraordinary aerosol conditions as well as seasonal differences. These studies show the potential of Polly NET to support the establishment of a global aerosol climatology that covers the entire troposphere.

deployed instrumented aircraft and ground-based measurements to elucidate causes of poor air quality related to high ozone and aerosol concentrations in South Korea. This work synthesizes data pertaining to aerosols (specifically, particulate matter with aerodynamic diameters <2.5 micrometers, PM 2.5) and conditions leading to violations of South Korean air quality standards (24-hr mean PM 2.5 < 35 µg m-3). PM 2.5 variability from AirKorea monitors across South Korea is evaluated. Detailed data from the Seoul vicinity are used to interpret factors that contribute to elevated PM 2.5. The interplay between meteorology and surface aerosols, contrasting synoptic-scale behavior vs. local influences, is presented. Transboundary transport from upwind sources, vertical mixing and containment of aerosols, and local production of secondary aerosols are discussed. Two meteorological periods are probed for drivers of elevated PM 2.5. Clear, dry conditions, with limited transport (Stagnant period), promoted photochemical production of secondary organic aerosol from locally emitted precursors. Cloudy humid conditions fostered rapid heterogeneous secondary inorganic aerosol production from local and transported emissions (Transport/Haze period), likely driven by a positive feedback mechanism where water uptake by aerosols increased gas-to-particle partitioning that increased water uptake. Further, clouds reduced solar insolation, suppressing mixing, exacerbating PM 2.5 accumulation in a shallow boundary layer. The combination of factors contributing to enhanced PM 2.5 is challenging to model, complicating quantification of contributions to PM 2.5 from local versus upwind precursors and production. We recommend co-locating additional continuous measurements at a few AirKorea sites across South Korea to help resolve this and other outstanding questions: carbon monoxide/carbon dioxide (transboundary transport tracer), boundary layer height (surface PM 2.5 mixing depth), and aerosol composition with aerosol liquid water (meteorologically-dependent secondary production). These data would aid future research to refine emissions targets to further improve South Korean PM 2.5 air quality.

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Abstract. Chemical effects on the size-resolved hygroscopicity of urban aerosols were examined based on the Korea–US Air Quality Study (KORUS-AQ, 2020) field campaign data. The information on size-resolved hygroscopicity and the chemical composition of aerosols were obtained by a hygroscopic tandem differential mobility analyzer (HTDMA) and a high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS), respectively. Good correspondence was shown between measured and estimated κ values calculated from the combination of bulk chemical composition data and oxidation parameters of organic aerosols (f44 and O∕C). These results imply that chemical composition is closely associated with aerosol hygroscopicity. However, the correlation between measured and estimated κ values degraded as particle size decreased, implying that size-resolved chemical composition data are required for more detailed hygroscopicity analysis. In addition to size-resolved chemical data, the m∕z tracer method was applied for size-resolved organic factors. Specifically, m∕z 57 and 44 were used as AMS spectral markers for hydrocarbon-like organic aerosol (HOA) and oxygenated organic aerosol (OOA), respectively. These size-resolved chemical composition data were found to be critical in explaining size-dependent hygroscopicity, as well as the diurnal variation in κ for small particles, i.e., low κ in the morning and high κ in the afternoon. Additionally, aerosol mixing state information was associated with the size-resolved chemical composition data. That is to say that the relationship between the number fraction of each hygroscopicity mode and the volume fraction of different chemical composition was investigated. For example, the HOA volume fraction comprised about 60 % of the variation in less hygroscopic (LH) mode number fractions for externally mixed aerosols.

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