Indian monsoon circulation is the primary driver of the long-range transboundary mercury (Hg) pollution from South Asia to the Himalayas and Tibet Plateau region, yet the northward extent of this transport remains unknown. In this study, a strong delta Hg-202 signature overlapping was found between Lake Gokyo and Indian anthropogenic sources, which is an indicative of the Hg source regions from South Asia. Most of the sediment samples were characterized with relatively large positive Delta Hg-199 values (mean = 0.07 parts per thousand-0.44 parts per thousand) and small positive Delta Hg-200 values (mean = 0.03 parts per thousand-0.08 parts per thousand). Notably, the Delta Hg-199 values in the lake sediments progressively increased from southwest to northeast. Moreover, the Delta Hg-199 values peaked at Lake Tanglha (mean = 0.44 parts per thousand +/- 0.04 parts per thousand) before decreased at Lake Qinghai that is under the influence of the westerlies. Our results suggest that transboundary atmospheric transport could transport Hg from South Asia northwards to at least the Tanglha Mountains in the northern Himalaya-Tibet.

Substituting alternative materials and energy sources with forest biomass can cause significant environmental consequences, such as alteration in the released emissions which can be described by displacement factors (DFs). Until now, DFs of wood-based materials have included greenhouse gas (GHG) emissions and have been associated with lower fossil and process-based emissions than non-wood counterparts. In addition to GHGs, aerosols released in combustion processes, for example, alter radiative forcing in the atmosphere and consequently have an influence on climate. In this study, the objective was to quantify the changes in the most important aerosol emission components for cases when wood-based materials and energy were used to replace the production of high-density polyethylene (HDPE) plastic, common fossil-based construction materials (concrete, steel and brick), non-wood textile materials and energy produced by fossil fuels and peat. For this reason, we expanded the DF calculations to include aerosol emissions of total suspended particles (TSP), respirable particulate matter (PM10), fine particles (PM2.5), black carbon (BC), nitrogen oxides (NOx), sulphur dioxide (SO2) and non-methane volatile organic compounds (NMVOCs) based on the embodied energies of materials and energy sources. The DFs for cardboard implied a decrease in BC, SO2 and NMVOC emissions but an increase in the other emission components. DFs for sawn wood mainly indicated higher emissions of both particles and gaseous emissions compared to non-wood counterparts. DFs for wood-based textiles demonstrated increased particle emissions and reduced gaseous emissions. DFs for energy biomass mainly implied an increase in emissions, especially if biomass was combusted in small-scale appliances. Our main conclusion highlights the critical need to thoroughly assess how using forest biomass affects aerosol emissions. This improved understanding of the aerosol emissions of the forestry sector is crucial for a comprehensive evaluation of the climate and health implications associated with forest biomass use.

Light-absorbing organic carbon (i.e., brown carbon, BrC) significantly contributes to light absorption and radiative forcing in the atmospheric particles. However, the secondary formation of BrC and optical properties of secondary BrC are poorly understood. In this study, we analyzed and evaluated the light absorption and environmental effects of BrC and secondary BrC from July 1st to 31st, 2022 (summer) and January 20th to February 20th, 2023 (winter) in Chongqing. BrC and secondary BrC light absorption were estimated via a seven- wavelength aethalometer and the statistical approach. The average values of secondary BrC light absorption (Abs(BrC,sec,lambda)) accounted for 46.2-56.5% of Abs(BrC). Abs(BrC,370) and Abs(BrC,sec,370) were significantly higher during winter (26.2 +/- 13.2 and 9.1 +/- 5.2 Mm(-1) respectively) than that during summer (7.2 +/- 4.1 and 5.2 +/- 3.5 Mm(-1) respectively) (p < 0.001), suggesting secondary formation played an essential role in BrC. A diurnal cycle of Abs(BrC,sec,370) was explained by the photobleaching of light-absorbing chromophores under the oxidizing conditions in the daytime, and the formation of chromophores via aqueous reactions with NH(4)(+ )and NO(x )after sunset during winter. PSCF analysis showed that transport of anthropogenic emissions from the northeastern and southeastern areas of Chongqing was the important source of the secondary BrC in PP during winter. During winter, the average values of SFEBrC and SFEBrC,sec were 31.9 and 27.4 W g(-1) lower than that during summer (64.7 and 44.5 W g(-1)), respectively. In contrast, J[NO2] values of SFEBrC and SFEBrC,sec decreased by 23.3% and 8.7% during winter higher than that during summer (19.9% and 5.6%), indicating that BrC and secondary BrC cause substantial radiative effects and atmospheric photochemistry. Overall, this study is helpful in understanding the characterization and secondary formation of BrC and accurately evaluating the environmental effects of BrC in Chongqing.

Aerosols affect Earth's climate both directly and indirectly, which is the largest uncertainty in the assessment of radiative forcings affecting anthropogenic climate change. The standard Aerosol Robotic Network (AERONET) aerosol products have been widely used for more than 30 years. Currently, there is strong community interest in the possibility of determining aerosol composition directly from remote sensing observations. This work presents the results of applying such a recently developed approach by Li et al. to extended datasets of the directional sky radiances and spectral aerosol optical depth (AOD) measured by AERONET for the retrievals of aerosol components. First, the validation of aerosol optical properties retrieved by this component approach with AERONET standard products shows good agreement. Then, spatiotemporal variations of the obtained aerosol component concentration are characterized globally, especially the absorbing aerosol species (black carbon, brown carbon, and iron oxides) and scattering aerosol species (organic carbon, quartz, and inorganic salts). Finally, we compared the black carbon (BC) and dust column concentration retrievals to the Modern-Era Retrospective Analysis for Research and Applications, version 2 (MERRA-2), products in several regions of interest (Amazon zone, Desert, and Taklamakan Desert) for new insights on the quantitative assessment of MERRA-2 aerosol composition products (R = 0.60-0.85 for BC; R = 0.75-0.90 for dust). The new value-added and long-term aerosol composition product globally is available online (https://doi.org/10.6084/ m9.figshare.25415239.v1), which provides important measurements for the improvement and optimization of aerosol modeling to enhance estimation of the aerosol radiative forcing. SIGNIFICANCE STATEMENT: In the assessment of climate change, the uncertainty associated with aerosol radiative forcing is the largest one. The purpose of this study is to provide a new value-added and long-term aerosol composition (including absorbing and scattering aerosol species) inversion dataset derived from Aerosol Robotic Network (AERONET) measurements for characterizing their spatiotemporal variations at global scale. We find some new insights on the quantitative assessment of black carbon and dust column concentration products in the Modern-Era Retrospective Analysis for Research and Applications, version 2 (MERRA-2). Our results and aerosol composition inversion dataset will provide robust support for the overall improvement and optimization of aerosol modeling to better understand the aerosol radiative forcing.

Vehicle -emitted fine particulate matter (PM 2.5 ) has been associated with significant health outcomes and environmental risks. This study estimates the contribution of traffic -related exhaust emissions (TREE) to observed PM 2.5 using a novel factorization framework. Specifically, co -measured nitrogen oxides (NO x ) concentrations served as a marker of vehicle -tailpipe emissions and were integrated into the optimization of a Non -negative Matrix Factorization (NMF) analysis to guide the factor extraction. The novel TREE-NMF approach was applied to long-term (2012 - 2019) PM 2.5 observations from air quality monitoring (AQM) stations in two urban areas. The extracted TREE factor was evaluated against co -measured black carbon (BC) and PM 2.5 species to which the TREE-NMF optimization was blind. The contribution of the TREE factor to the observed PM 2.5 concentrations at an AQM station from the first location showed close agreement ( R 2 = 0 .79) with monitored BC data. In the second location, a comparison of the extracted TREE factor with measurements at a nearby Surface PARTiculate mAtter Network (SPARTAN) station revealed moderate correlations with PM 2.5 species commonly associated with fuel combustion, and a good linear regression fit with measured equivalent BC concentrations. The estimated concentrations of the TREE factor at the second location accounted for 7 - 11 % of the observed PM 2.5 in the AQM stations. Moreover, analysis of specific days known to be characterized by little traffic emissions suggested that approximately 60 - 78 % of the traffic -related PM 2.5 concentrations could be attributed to particulate traffic -exhaust emissions. The methodology applied in this study holds great potential in areas with limited monitoring of PM 2.5 speciation, in particular BC, and its results could be valuable for both future environmental health research, regional radiative forcing estimates, and promulgation of tailored regulations for traffic -related air pollution abatement.

In this study, air pollutants were analyzed at a low-industry city on the Silk Road Economic Belt of Northwestern China from 2015 to 2018. The results show that SO2 and CO had a decreasing trend and NO2, O-3, PM2.5, and PM10 had an increasing trend during the study period. The primary characteristic pollutants were PM2.5 and PM10, which were higher than China's Grade II standard. SO2, NO2, CO, PM2.5, and PM10 concentrations showed similar seasonal variation patterns: the highest pollutant concentration was in winter and the lowest in summer. Those pollutants showed a similar diurnal pattern with two peaks, one at 7:00 to 9:00 and another at 21:00 to 22:00. However, O-3 concentration was highest in summer and lowest in winter, with a unimodal diurnal variation pattern. The annual average pollution concentrations in Tianshui in 2017 were substantially lower than the concentrations reported by most cities in China. By examining the meteorological conditions at a daily scale, we found that Tianshui was highly influenced by local emissions and a southwest wind. Potential source contributions and concentration weighted trajectory analyses indicated that the pollution from Gansu, Sichuan, Qinghai, and Shaanxi Province could affect the pollution concentration in Tianshui. The results provide directions for the government to take in formulating regional air pollution prevention and control measures and to improve air quality.

Aerosol optical and radiative properties play a key role in climate change. Precisely pinpointing the optical and radiative properties of various types of aerosols during diverse pollution events in urban settings remains a challenge. In this study, aerosol optical and radiative properties under contrasting pollution conditions were investigated, including dusty, haze, fireworks, and clean days, in a typical urban valley in Northwestern China, based on observations from the Sun-Sky photometers and simulations from libRadtran. The results show that on dusty days aerosols have high absorption and low backscattering, while on haze days they are characterized by fine, absorptive organic aerosol particles with pronounced forward scattering in the ultraviolet and visible spectra. On fireworks days during Chinese New Year (CNY), fine-mode aerosols from fireworks dominate, with the highest scattering and the lowest absorption under the four pollution conditions, and the particle peak radius growth responds rapidly to changes in relative humidity. Aerosols generally cause Earth's surface cooling and atmospheric warming across various pollution conditions. Notably, dusty days, clean days, and haze days all exhibit a lower positive aerosol radiative forcing (ARF) in the ultraviolet (UV) spectrum at the top of the atmosphere (TOA) due to lower single-scattering albedo (SSA). In contrast, CNY uniquely displays negative UV_ARF at TOA, attributed to high-SSA non-absorptive particles. Aerosols on dusty days have higher positive radiative forcing than on haze days, emphasizing the absorptive impact of mixed dust aerosols. These findings provide valuable insights into the behavior of aerosols under various pollution conditions in a typical urban valley, contributing to a better understanding of the environmental effects of various aerosols in arid urban regions.

In the early 21st century, Southwest China (SWC) frequently experienced extreme droughts and severe haze pollution events. Although the meteorological causes of these extreme droughts have been widely investigated, previous studies have yet to understand the causes of haze pollution events over SWC. Moreover, the associations between winter atmospheric teleconnections during drought and haze pollution event across SWC has received negligible attention and therefore warrants investigation. This study examines the associations between the atmospheric teleconnections with respect to winter droughts and winter haze pollution over SWC. Our main conclusions are as follows. (1) Winter precipitation and winter haze days (WHD) over SWC had three major fluctuations from 1959 to 2016. (2) The atmospheric circulation pattern over the Eurasian (EU) continent associated with WHD over SWC resembled that of winter droughts over SWC, where both can be characterized by an EU teleconnection pattern. The Arctic Oscillation (AO) mainly induced the atmospheric circulation pattern over the EU continent that is associated with WHD over SWC. (3) The sea surface temperature (SST) and low circulation anomalies in the Pacific and north Atlantic associated with WHD were similar to those associated with winter droughts over SWC. La Nina events and negative phases of the North Atlantic Oscillation (NAO) may induce winter drought and increase the WHD over SWC. (4) Compared with winter drought over SWC, the variation in the WHD was more complex and the factors affecting WHD were more diverse, and winter drought and its related atmospheric circulations were important factors that induced haze pollution over SWC. Overall, this study not only fills a gap in the literature with respect to the associations between the atmospheric teleconnections of winter drought and winter haze pollution over SWC, but also provides an important scientific basis for the development of potential predictions of local monthly haze pollution, which improves the forecast accuracy of local short-term haze pollution and enriches the theoretical understanding of the meteorological causes of local haze pollution. (C) 2020 Elsevier B.V. All rights reserved.

Progressive climate change may have unpredictable consequences for the Arctic environment. Permafrost catchments off the west coast of Svalbard, described as thin and warm, are particularly sensitive to climate change. The interdisciplinary research on the hydrochemical response of surface and underground water functioning within a small permafrost catchment area focused on the determination of the impact of meteorological conditions (temperature (T), precipitation (P)) on the mean daily discharge (Q), and the lowering of the groundwater table (H). We determined physical and chemical properties (pH and SEC) and concentrations of major elements (Ca, Mg, Na, K) and 23 trace elements (i.a. Cd, Cu, Hg, Pb, Zn) in 280 water samples. The results of the correlation matrix showed that an increase in the average air temperature in the summer of 2021 had a significant impact on the hydrochemistry of both types of waters operating in the catchment. In response to increase in T, the lowering of the H (0.52 < r < 0.66) and a decrease in Q (-0.66 < r < -0.68) were observed what in consequence also leads to changes in water chemistry. The principal component analysis (CA) indicates that chemical weathering and binding of elements to DOC are processes influencing water chemistry. Results of statistical analysis showed that the resultant of the hydrometeorological conditions that prevailed in that season and the type of geological formations on which they were located had a significant impact on the water chemistry at individual measurement points. Significant differences in the concentrations of elements between points on the same geological formations were also found.

The concentration and isotopic composition of mercury (Hg) were studied in frozen soils along a southwest-northeast transect over the Himalaya-Tibet. Soil total Hg (Hg-T) concentrations were significantly higher in the southern slopes (72 +/- 54 ng g(-1), 2SD, n = 21) than those in the northern slopes (43 +/- 26 ng g(-1), 2SD, n = 10) of Himalaya-Tibet. No significant relationship was observed between Hg T concentrations and soil organic carbon (SOC), indicating that the Hg-T variation was not governed by SOC. Soil from the southern slopes showed significantly negative mean delta Hg-202 (-0.53 +/- 0.50 parts per thousand, 2SD, n = 21) relative to those from the northern slopes (-0.12 +/- 0.40 parts per thousand, 2SD, n = 10). The delta Hg-202 values of the southern slopes are more similar to South Asian anthropogenic Hg emissions. A significant correlation between 1/Hg-T and delta Hg-202 was observed in all the soil samples, further suggesting a mixing of Hg from South Asian anthropogenic emissions and natural geochemical background. Large ranges of Delta Hg-199 (-0.45 and 0.24 parts per thousand) were observed in frozen soils. Most of soil samples displayed negative Delta Hg-199 values, implying they mainly received Hg from gaseous Hg(0) deposition. A few samples had slightly positive odd-MIF, indicating precipitation-sourced Hg was more prevalent than gaseous Hg(0) in certain areas. The spatial distribution patterns of Hg-T concentrations and Hg isotopes indicated that Himalaya-Tibet, even its northern part, may have been influenced by transboundary atmospheric Hg pollution from South Asia. (C) 2019 Elsevier Ltd. All rights reserved.