Insights on aerosol properties using two decades-long ground-based remote sensing datasets in Moldova, Eastern Europe.

Aerosol optical properties were studied over Chisinau in Moldova, one of the longest running AERONET sites in Eastern Europe. During two decades (September 1999-November 2018), the mean aerosol optical depth (AOD) and Angstrom exponent (AE) were observed as 0.21 ± 0.13 and 1.49 ± 0.29, respectively. The highest AOD (0.24 ± 0.13) and AE (1.60 ± 0.26) were observed during the summer. More than half (∼55%) of the share was occupied by clean continental aerosols with seasonal order of winter (74.8%) > autumn (62%) > spring (48.9%) > summer (44.8%) followed by mixed aerosols with a respective contribution of 30.7% (summer), 28.4% (spring), 22.5 (autumn) and 16.4% (winter). A clear dominance of volume size distribution in the fine mode indicated the stronger influence of anthropogenic activities resulting in fine aerosol load in the atmosphere. The peak in the fine mode was centered at 0.15 µm, whereas that of the coarse mode was centered either at 3.86 µm (summer and autumn) or 5.06 µm (spring and winter). 'Extreme' aerosol events were observed during 21 days with a mean AOD (AE) of 0.99 ± 0.32 (1.43 ± 0.43), whereas 'strong' events were observed during 123 days with a mean AOD (AE) of 0.57 ± 0.07 (1.44 ± 0.40), mainly influenced by anthropogenic aerosols (during 19 and 101 days of each event type) from urban/industrial and biomass burning indicated by high AE and fine mode fraction. During the whole period (excluding events days), the fine and coarse mode peaks were observed at the radius of 0.15 and 5.06 µm, which in the case of extreme (strong) events were at 0.19 (0.15) and 3.86 (2.24) µm respectively. The fine mode volume concentration was 4.78 and 3.32 times higher, whereas the coarse mode volume concentration was higher by a factor of 1.98 and 2.27 during extreme and strong events compared to the whole period.

Seasonal source identification and formation processes of marine particulate water soluble organic nitrogen over an offshore island in the East China Sea.

Water soluble organic nitrogen (WSON) had great influences on the aerosol chemistry, hygroscopicity, marine primary productivity, as well as nitrogen biogeochemical cycles. Aerosol sampling was conducted over an offshore island in the East China Sea in four seasons of 2019, aiming to reveal the seasonal sources and secondary formation processes of marine WSON. The annual mean WSON concentration reached 1.05 ± 1.72 µg/m3 with a mean WSON/WSTN fraction of 27 %. In spring, WSON was associated with combustion emissions. The liquid-phase reaction of NH3/NH4+ with VOCs was a potential secondary formation process of WSON. In summer, WSON was mainly formed through the gaseous phase oxidation of marine biogenic precursors. In autumn, WSON showed miscellaneous sources from agricultural activities, biomass burning, and fossil fuel combustion. In addition to the contribution from primary urea, WSON could be also affected by the oxidation of biological proteinaceous matters. This explained the highest WSON concentrations and WSON/WSOC ratios in autumn. In winter, WSON was probably emitted from sea spray aerosols via the bubble-bursting processes. This study indicated that the sources of WSON over the coastal waters in the East China Sea were quite diverse, highlighting the need of more detailed characterization of marine WSON at the molecular level.

Characterization of columnar aerosol over a background site in Central Asia.

Ground-based observational characterization of atmosphere aerosols over Central Asia is very limited. This study investigated the columnar aerosol characteristics over Issyk-Kul, Kyrgyzstan, a background site in Central Asia using the long-term (∼14 years: August 2007-November 2021) data acquired with the Cimel sunphotometer. The mean aerosol optical depth (AOD) and Ångström exponent (AE) during the observation period were 0.14 ± 0.10 and 1.19 ± 0.41, respectively. Both AOD and AE varied across seasons, with highest AOD in spring (0.17 ± 0.17). Regarding the aerosol types, clean continental aerosols were dominant type (65%), followed by mixed aerosols (∼19%), clean marine aerosols (∼14%), dust (0.8%), and urban/industrial and biomass burning aerosol (0.7%). The aerosol volume size distribution was bimodal indicating the influence of both anthropogenic and natural aerosols with clear dominance of coarse mode during the spring season. Mainly dust and mixed aerosols were present during high aerosol episodes while the coarse mode aerosol volume concentration was 7.5 (strong episodes) and ∼19 (extreme episodes) times higher than the whole period average. Aerosol over this background sites were from local and regional sources with some contribution of long-range transport.

Organic aerosol compositions and source estimation by molecular tracers in Dushanbe, Tajikistan.

To elucidate the molecular composition and sources of organic aerosols in Central Asia, carbonaceous compounds, major ions, and 15 organic molecular tracers of total suspended particulates (TSP) were analyzed from September 2018 to August 2019 in Dushanbe, Tajikistan. Extremely high TSP concentrations (annual mean ± std: 211 ± 131 µg m-3) were observed, particularly during summer (seasonal mean ± std: 333 ± 183 µg m-3). Organic carbon (OC: 11.9 ± 7.0 µg m-3) and elemental carbon (EC: 5.1 ± 2.2 µg m-3) exhibited distinct seasonal variations from TSP, with the highest values occurring in winter. A high concentration of Ca2+ was observed (11.9 ± 9.2 µg m-3), accounting for 50.8% of the total ions and reflecting the considerable influence of dust on aerosols. Among the measured organic molecular tracers, levoglucosan was the predominant compound (632 ± 770 ng m-3), and its concentration correlated significantly with OC and EC during the study period. These findings highlight biomass burning (BB) as an important contributor to the particulate air pollution in Dushanbe. High ratios of levoglucosan to mannosan, and syringic acid to vanillic acid suggest that mixed hardwood and herbaceous plants were the main burning materials in the area, with softwood being a minor one. According to the diagnostic tracer ratio, OC derived from BB constituted a large fraction of the primary OC (POC) in ambient aerosols, accounting for an annual mean of nearly 30% and reaching 63% in winter. The annual contribution of fungal spores to POC was 10%, with a maximum of 16% in spring. Measurements of plant debris, accounting for 3% of POC, divulged that these have the same variation as fungal spores.

Significant Influence of Carbonates on Determining Organic Carbon and Black Carbon: A Case Study in Tajikistan, Central Asia.

Carbonates cause large uncertainties in determining the concentrations of organic carbon (OC) and elemental carbon (EC), as well as EC's light absorption characteristics, in arid locations, such as Central Asia. To investigate this influence, a comparison between acid (HCl)-treated and original total suspended particle (TSP) samples was conducted in Dushanbe, Tajikistan. According to the results, the OC and EC concentrations were overestimated by approximately 22.8 ± 33.8 and 32.5 ± 33.5%, with the actual values being 11.9 ± 3.0 and 5.13 ± 2.24 µg m-3, respectively. It was found that carbonates had a larger influence from May to October than during the other months, which was significantly correlated with the amount of TSPs on the filter. Furthermore, the mass absorption cross-section of EC (MACEC) increased from 4.52 ± 1.32 to 6.02 ± 1.49 m2 g-1; this indicated that carbonates can significantly decrease MACEC, thus causing an underestimation of approximately 23.9 ± 16.7%. This is the first study that quantifies the influence of carbonates on the light-absorbing abilities of EC.

Columnar aerosol properties and radiative effects over Dushanbe, Tajikistan in Central Asia.

This paper presents the results of the study on columnar aerosol optical and physical properties and radiative effects directly observed over Dushanbe, the capital city of Tajikistan, a NASA AERONET site (equipped with a CIMEL sunphotometer) in Central Asia. The average aerosol optical depth (AOD) and Ångström exponent (AE) during the observation period from July 2010 to April 2018 were found to be 0.28 ± 0.20 and 0.82 ± 0.40, respectively. The highest seasonal AOD (0.32 ± 0.24), accompanied by the lowest average AE (0.61 ± 0.25) and fine-mode fraction in AOD (0.39), was observed during summer due to the influence of coarse particles like dust from arid regions. Fine particles were found in significant amounts during winter. The 'mixed aerosol' was identified as the dominant aerosol type with presence of 'dust aerosol' during summer and autumn seasons. Aerosol properties like volume size distribution, single scattering albedo, asymmetry parameter and refractive index suggested the influence of coarse particles (during summer and autumn). Most of the air masses reaching this site transported local and regional emissions, including from beyond Central Asia, explaining the presence of various aerosol types in Dushanbe's atmosphere. The seasonal aerosol radiative forcing efficiency (ARFE) in the atmosphere was found high (>100 Wm-2) and consistent throughout the year. Consequently, this resulted in similar seasonally coherent high atmospheric solar heating rate (HR) of 1.5 K day-1 during summer-autumn-winter, and ca. 0.9 K day-1 during spring season. High ARFE and HR values indicate that atmospheric aerosols could exert significant implications to regional air quality, climate and cryosphere over the central Asian region and downwind Tianshan and Himalaya-Tibetan Plateau mountain regions with sensitive ecosystems.