Aerosol microphysical properties, scattering and absorption characteristics, and in particular, the vertical distributions of these parameters over the eastern Loess Plateau, were analyzed based on aircraft measurements made in 2020 during a summertime aircraft campaign in Shanxi, China. Data from six flights were analyzed. Statistical characteristics and vertical distributions of aerosol concentration, particle size, optical properties, including aerosol scattering coefficient (Sigma sp), backscattering ratio (beta sc), Angstro spacing diaeresis m exponent (alpha), single-scattering albedo (SSA), partially-integrated aerosol optical depth (PAOD), and black carbon concentration (BCc), were obtained and discussed. Mean values of aerosol particle number concentration (Na), particle volume concentration (Va), mass concentration (Ma), surface concentration (Sa), and particle effective diameter (EDa) were 854.92 cm-3, 13.37 mu m3 cm- 3, 20.06 mu g/m3, 170.08 mu m3 cm- 3, and 0.47 mu m, respectively. Mean values of BCc, Sigma sp (450, 525, 635 nm), beta sp (525 nm), alpha(635/450), and SSA were 1791.66 ng m- 3, 82.37 Mm- 1 at 450 nm, 102.57 Mm- 1 at 525 nm, 126.60 Mm-1 at 635 nm, 0.23, 1.47, and 0.92, respectively. Compared with values obtained in 2013, Na decreased by 60% and Ma decreased by 45%, but the scattering coefficients increased in different degrees. In the vertical direction, aerosol concentrations were higher at lower altitudes, decreasing with height. Vertical profiles of Sigma sp, beta sp, alpha(635/450), and BCc measured during the six flights were examined. Two peaks in Na were identified near the top of the boundary layer and between 2000 and 2200 m. Fine particles with EDa smaller than 0.8 mu m are dominant in the boundary layer and coarse aerosols existed aloft. Aerosol scattering properties and BCc in the lowest layer of the atmosphere contributed the most to the total aerosol radiative forcing. SSA values were greater than 0.9 below 2500 m, with lower values at higher levels of the atmosphere. On lightly foggy days, SSA values were greater than 0.9, and aerosols played a cooling role in the atmosphere. On hazy days, lowerlevel SSA values were generally greater than 0.85, with aerosols likely having a warming effect on the atmosphere. 48-hour backward trajectories of air masses during the observation days showed that the majority of aerosol particles in the lower atmosphere originated from local or regional pollution emissions, contributing the most to the total aerosol loading and leading to high values of aerosol concentration and radiative forcing.

Equivalent black carbon (EBC) was measured with a seven-wavelength Aethalometer (AE-31) in the Urumqi River Valley, eastern Tien Shan, China. This is the first high-resolution, online measurement of EBC conducted in the eastern Tien Shan allowing analysis of the seasonal and hourly variations of the light absorption properties of EBC. Results showed that the highest concentrations of EBC were in autumn, followed by those in summer. The hourly variations of EBC showed two plateaus during 8:00-9:00 h local time (LT) and 16:00-19:00 h LT, respectively. The contribution of biomass burning to EBC in winter and spring was higher than in summer and autumn. The planetary boundary layer height (PBLH) showed an inverse relationship with EBC concentrations, suggesting that the reduction of the PBLH leads to enhanced EBC. The aerosol optical depths (AOD) over the Urumqi River Valley, derived from the Moderate Resolution Imaging Spectroradiometer (MODIS) data and back trajectory analysis, showed that the pollution from Central Asia was more likely to affect the atmosphere of Tien Shan in summer and autumn. This suggests that long-distance transported pollutants from Central Asia could also be potential contributors to EBC concentrations in the Urumqi River Valley, the same as local anthropogenic activities.

Water-soluble brown carbon (BrC) plays an important role in climate change by influencing aerosol radiative forcing. There is little information on aerosol BrC over the South China Sea (SCS). In this study, water-soluble organic carbon (WSOC) in a round-year set of aerosol samples from a remote island in the northern SCS were characterized for optical properties. In-depth information about the sources and input pathways of water-soluble BrC was obtained using molecular markers and statistic tools. The highest WSOC concentrations, light absorption coefficients at 365 nm (Abs(365)) and mass absorption efficiencies at 365 nm (MAE(365)) were observed in winter when atmospheric outflow from mainland China and the northern Indo-China Peninsula prevailed. Through the year, primary emissions from biomass burning and urban secondary organic aerosols (SOA) & waste combustion, respectively, were observed to be associated with higher MAE(365) (2.47 +/- 0.40 m(2) g(-1) and 1.97 +/- 0.22 m(2) g(-1)) and to be the main contributors to Abs(365) (22.0 +/- 3.6% and 31.6 +/- 3.6%), while biogenic SOA showed little contribution. For the first time, microorganism/plankton primary emissions, mainly from the sea, was identified to be an important contributor to water-soluble BrC (13.6 +/- 4.2% of Abs(365), MAE(365): 0.98 +/- 0.30 m(2) g(-1)), especially in spring (31% of Abs(365)). This implies that emissions from microorganism/plankton warrants careful consideration in the assessment of global aerosol light absorbance.

Dissolved organic carbon (DOC) in snow plays an important role in river ecosystems that are fed by snowmelt water. However, limited knowledge is available on the DOC content in snow of the Chinese Altai Mountains in Central Asia. In this study, DOC in the snow cover of the Kayiertesi river basin, southern slope of Altai Mountains, was investigated during November 2016 to April 2017. The results showed that average concentrations of DOC in the surface snowcover (1.01 +/- 0.52 mgL(-1)) were only a little higher than those in glaciers of the Tibetan Plateau, European Alps, and Alaska, but much higher than in Greenland Ice Sheet. Depth variations of DOC concentrations from snowpack profiles indicated higher values in the surface layer. During the observation period, scavenging efficiency for DOC in snow cover is estimated to be 0.15 +/- 0.10, suggesting that DOC in snow can be affected more by the meltwater during ablation season than during accumulation season. The average mass absorption cross at 365 nm and the absorption Angstrom exponent of DOC were 0.45 +/- 0.35 m(2) g(-1) and 2.59 +/- 1.03, respectively, with higher values in March and April 2017. Fraction of radiative forcing caused by DOC relative to black carbon accounted for about 10.5%, implying DOC is a non-ignorable light-absorber of solar radiation in snow of the Altai regions. Backward trajectories analysis and aerosol vertical distribution images from satellites showed that DOC in the snow of the Altai Mountains was mainly influenced by air masses from Central Asia, Western Siberia, the Middle East, and some even from Europe. Biomass burning and organic carbon mixed with mineral dust contributed significantly to the DOC concentration. This study highlights the effects of DOC in the snow cover for radiative forcing and the need to study carbon cycling for evaluation of quality of the down-streams ecosystems. (c) 2018 Elsevier B.V. All rights reserved.

Recent ground-based measurements reveal that model-based observations are underestimating absorption properties and direct radiative forcing (DRF) due to carbonaceous species by a factor of 2-3 over South and East Asia. Thus, to better constraint these parameters associated with carbonaceous species, seasonal variability records through ground-based measurements are very essential. In this context, we report herein the absorption properties of water-extractable brown carbon (BrC), elemental carbon (EC), and BrC + EC and DRF of BrC and BrC + EC (relative to EC) over the Indo-Gangetic Plain (IGP) during a weak monsoon season [July-September 2015; influenced by El Nino and PDO (Pacific Decadal Oscillation)]. PM2.5 (particulate matter with aerodynamic diameter <= 2.5 mu m) samples (n = 31) have been assessed from central IGP location at Kanpur. Absorption coefficient at 365 nm (b(abs-365)) of BrC, EC, and BrC + EC centers at 3.6, 8.1, and 11.4 Mm(-1), respectively. Strong linear regression correlation (R = 0.8) of b(abs-365) of BrC with sea-salt and mineral dust corrected potassium (K-BB(+)) indicates biomass burning as the predominant source of BrC over the region in this study. Synergistic effect in b(abs) of BrC + EC (relative to that of EC) increases conspicuously (enhanced by a factor varying from 1.05 to 1.21) with an increase in wavelength from UV (365 nm) to visible region (660 nm). DRF (relative to EC) of BrC during monsoon season ranges from 3.9 to 23.8 (13.0 +/- 5.0) %, whereas total DRF (BrC + EC) ranges from 111.0 to 148.2 (126.6 +/- 10.0) %. Individual contribution of BrC and EC to total DRF has been estimated as 10 and 79.5%, respectively. The remaining contribution (10.5%) to total DRF has been attributed to synergism in absorption properties (i.e., b(abs)) of BrC + EC.