Aerosol optical properties, including absorption and scattering coefficients (B-abs, and B-scat), extinction coefficient (B-ext), single scattering albedo (SSA), and so forth, are critical metrics to estimate the radiative balance of the atmosphere. However, their ground measurements are sparsely distributed in the world, where Central Asia is void in these measurements. We had been performing the measurements of AOPs and BC with a photoacoustic extinctiometer (PAX) in Jimunai, a border town of China neighboring Kazakhstan, Central Asia, from Aug 2016 to Apr 2019. This three-year study first reported statistically significant trends of B-abs, B-scat, B-ext, SSA, and derived concentrations of BC (Mann-Kendall trend test, p-value 0.05) in the Central-Asian area. B-abs and B-scat show increasing trends and SSA was decreasing determined by the greater increasing pace of B-abs than B-scat. Seasonal and diurnal variations of the AOPs were associated with climate shift and residents' commute activity, respectively. The difference in the magnitudes and trends of AOPs between the measurements and satellites' observations advise that more care should be invested when choosing remote-sensing data to represent the AOPs at a specific site. The increasing trend of derived BC concentrations is reflected in the deposition record of BC in a snowpit of the nearby Muz Taw glacier. We suppose that the dramatically increasing BC particles emitted from Jimunai are significant factors triggering the melting of the adjacent mountain glaciers. The outflow of dust from the neighboring Gurbantiinggiit Desert could occasionally invade into Jimunai and deteriorate the local air quality, as evidenced by a probable dust event captured by the PAX on Feb 15, 2018. Finally, we outlook the future perspectives of measurements in Jimunai as a long-standing station.

Since aerosols are an integral part of the Arctic climate system, understanding aerosol radiative properties and the relation of these properties to each other is important for constraining aerosol radiative forcing effects in this remote region where measurements are sparse. In situ measurements of aerosol size distribution, aerosol light scattering and absorption were taken near Eureka (80.05 degrees N, 86.42 degrees W), on Ellesmere Island, in the Canadian High Arctic over three consecutive years to provide insights into radiative properties of Arctic aerosols. During periods of Arctic haze, we find that the single scattering albedo (SSA) at 405 nm is generally higher and more stable than that determined at 870 nm, with values ranging between 0.90-0.99 and 0.79-0.97, respectively. Events with elevated absorption coefficients (B-abs) exhibit generally an absorption Angstrom exponent (AAE) of around 1 suggesting that black carbon (BC) is the dominant absorbing aerosol for the measurement period. AAE values close to 2 occurring with scattering Angstrom exponent (SAE) values near 0 and SAE values below 0 occasionally observed in December indicate a potential contribution from mineral dust aerosols in late fall and early winter. The apparent real and imaginary parts of the complex refractive index at 405 nm have been found to range between 1.6-1.9 and 0.002-0.02, respectively. The low imaginary component indicates very weak intrinsic absorption compared to BC-rich aerosols. Systematic variabilities between different aerosol optical and microphysical properties depend strongly on the given wavelength. SSA at 405 nm shows a strong inverse dependence with B-abs, because B-abs correlates positively with the imaginary component of the refractive index. On the other hand, SSA at 870 nm correlates with scattering coefficient (B-sca) and not with B-abs due to a greater sensitivity to the ambient particle size distribution for 870 nm scattering. Smaller particles with higher SAE that are prevalent during less polluted periods only weakly scatter at 870 nm leading to lower SSA when B-sca is also low. Lastly, FLEXPART back-trajectories show that lower aerosol SSA and higher B-abs correspond to air masses which are more influenced by Eurasian and Alaskan regions, including regions known to have important BC emissions. This work emphasizes the important variability in Arctic aerosol optical properties during winter and spring, which is likely due to changes in source regions.