Char and soot represent distinct types of elemental carbon (EC) with varying sources and physicochemical properties. However, quantitative studies in sources, atmospheric processes and light-absorbing capabilities between them remain scarce, greatly limiting the understanding of EC's climatic and environmental impacts. For in-depth analysis, concentrations, mass absorption efficiency (MAE) and stable carbon isotope were analyzed based on hourly samples collected during winter 2021 in Nanjing, China. Combining measurements, atmospheric transport model and radiative transfer model were employed to quantify the discrepancies between char-EC and soot-EC. The mass concentration ratio of char-EC to soot-EC (R-C/S) was 1.4 +/- 0.6 (mean +/- standard deviation), showing significant dependence on both source types and atmospheric processes. Case studies revealed that lower R-C/S may indicate enhanced fossil fuel contributions, and/or considerable proportions from long-range transport. Char-EC exhibited a stronger light-absorbing capability than soot-EC, as MAE(char) (7.8 +/- 6.7 m(2)g(-1)) was significantly higher than MAE(soot) (5.4 +/- 3.4 m(2)g(-1))(p < 0.001). Notably, MAE(char) was three times higher than MAE(soot) in fossil fuel emissions, while both were comparable in biomass burning emissions. Furthermore, MAE(soot) increased with aging processes, whereas MAE(char) exhibited a more complex trend due to combined effects of changes in coatings and morphology. Simulations of direct radiative forcing (DRF) for five sites indicated that neglecting the char-EC/soot-EC differentiation could cause a 10 % underestimation of EC's DRF, which further limit accurate assessments of regional air pollution and climate effects. This study underscores the necessity for separate parameterization of two types of EC for pollution mitigation and climate change evaluation.

Light-absorbing impurities (LAIs), such as mineral dust (MD), organic carbon (OC), and black carbon (BC), deposited in snow, can reduce snow albedo and accelerate snowmelt. The Ili Basin, influenced by its unique geography and westerly atmospheric circulation, is a critical region for LAI deposition. However, quantitative assessments on the impact of LAIs on snow in this region remain limited. This study investigated the spatial distribution of LAIs in snow and provided a quantitative evaluation of the effects of MD and BC on snow albedo, radiative forcing, and snowmelt duration through sampling analysis and model simulations. The results revealed that the Kunes River Basin in the eastern Ili Basin exhibited relatively high concentrations of MD. In contrast, the southwestern Tekes River Basin showed relatively high concentrations of OC and BC. Among the impurities, MD plays a dominant role in the reduction of snow albedo and has a greater effect on the absorption of solar radiation by snow than BC, while MD is the most important light-absorbing impurity responsible for the reduction in the number of snow-melting days in the Ili Basin. Under the combined influence of MD and BC, the snowmelt period in the Ili Basin was reduced by 2.19 +/- 1.43 to 7.31 +/- 4.76 days. This study provides an initial understanding of the characteristics of LAIs in snow and their effects on snowmelt within the Ili Basin, offering essential basic data for future research on the influence of LAIs on snowmelt runoff and hydrological processes in this region.

Aerosol absorption and scattering notably influence the atmospheric radiative balance. Significant uncertainties persist regarding the impact of aerosol models on aerosol radiative forcing (ARF) under distinct atmospheric conditions. The effects of various aerosol models on ARF under clear and haze conditions are analyzed utilizing MODIS data, combined with observations from Beijing, and the 6S (Second Simulation of the Satellite Signal in the Solar Spectrum) for simulations. Results showed that ARF at the surface (ARF-SFC) and top of the atmosphere (ARF-TOA) registered negative values on clear and hazy days. On hazy days, the desert model demonstrated enhanced cooling at TOA, while the urban model showed intensified surface cooling. Hazy conditions amplified ARF-TOA by 57%, 54%, and 61% for desert, urban, and continental models respectively, relative to clear days, with corresponding ARF-SFC increases of 57%, 54%, and 56%. Aerosol radiative forcing efficiency at TOA generally exhibited greater values in winter than in summer. Black carbon (BC) radiative forcing simulations using the three-component method showed positive values at TOA and negative values at the surface. During hazy days, BC intensified upper-atmosphere heating and surface cooling effects. This research will lay the scientific foundation for reducing uncertainty in ARF estimates and developing effective environmental strategies.

Altitude profiles of the mass concentrations of aerosol black carbon (BC) have been obtained,up to an altitude of 12 km, from in situ measurements over Hyderabad (17.47 degrees N, 78.57 degrees E, 557 m amsl;a tropical station in the central Indian peninsula), using three successive high altitude balloon ascents during winter and early summer seasons of 2023-2024. The profiles revealed predominant peaks at around 8 and 11 km, where the BC concentrations were reaching as high as nearly three times the surface concentrations (2.82, 2.76, and 2.60 mu g m-3, respectively), persistently in all the three flights. Detailed analyses using official data of air traffic movement, aviation statistics and emission inventory revealed a strong linkage with the emissions from commercial aircraft that touch Hyderabad and overfly the region. These elevated BC layers will have large implications to atmospheric radiative forcing and possible contributions to modification of the cirrus cloud properties.

Air pollution is a global health issue, and events like forest fires, agricultural burning, dust storms, and fireworks can significantly worsen it. Festivals involving fireworks and wood-log fires, such as Diwali and Holi, are key examples of events that impact local air quality. During Holi, the ritual of Holika involves burning of biomass that releases large amounts of aerosols and other pollutants. To assess the impact of Holika burning, observations were conducted from March 5th to March 18th, 2017. On March 12th, 2017, around 1.8 million kg of wood and biomass were openly burned in about 2250 units of Holika, located in and around the Varanasi city (25.23 N, 82.97 E, similar to 82.20 m amsl). As the Holika burning event began the impact on the Black Carbon (BC), particulate matter 10 & 2.5 (PM10 and PM2.5), sulphur dioxide (SO2), oxides of nitrogen (NOx), ozone (O-3) and carbon monoxide (CO) concentration were observed. Thorough optical investigations have been conducted to better comprehend the radiative effects of aerosols produced due to Holika burning on the environment. The measured AOD at 500 nm values were 0.315 +/- 0.072, 0.392, and 0.329 +/- 0.037, while the BC mass was 7.09 +/- 1.78, 9.95, and 7.18 +/- 0.27 mu g/m(3) for the pre-Holika, Holika, and post-Holika periods. Aerosol radiative forcing at the top of the atmosphere (ARF-TOA), at the surface (ARF-SUR), and in the atmosphere (ARF-ATM) are 2.46 +/- 4.15, -40.22 +/- 2.35, and 42.68 +/- 4.12 W/m(2) for pre-Holika, 6.34, -53.45, and 59.80 W/m(2) for Holika, and 5.50 +/- 0.97, -47.11 +/- 5.20, and 52.61 +/- 6.17 W/m(2) for post-Holika burning. These intense observation and analysis revealed that Holika burning adversely impacts AQI, BC concentration and effects climate in terms of ARF and heating rate.

Wet scavenging of black carbon (BC) is essential for evaluating their atmospheric lifetime and radiative forcing. However, it is crucial to differentiate atmospheric BC into char and soot subgroups, given their significant disparities in physicochemical properties and potential impacts. We first conducted a comparative study of char/soot in PM10 and rainwater, collected over a year in urban Guangzhou, China. The mean char/soot ratio in PM10 (similar to 2.5) is obviously higher than that in rainwater (similar to 0.8), corresponding to higher wet scavenging efficiency of soot. Through sequence rainwater sampling during individual rainfall events, we further distinguished the contributions of in-cloud and below-cloud scavenging, with in-cloud scavenging predominantly contributed to the distinct difference between char and soot. Such a distinct wet scavenging behavior of char and soot would have substantial implications for the atmospheric behavior of BC, which should be considered in future models for accurate evaluation of its lifetime and climate impact.

This study investigates aerosol characteristics using ground-based measurements at two distinct regions, MohalKullu (31.9 degrees N, 77.12 degrees E; 1154 m amsl) and Kosi-Katarmal (29.64 degrees N, 79.62 degrees E; 1225 m amsl), from July 2019 to June 2022. The average Black Carbon (BC) concentrations were 1.5 f 1.0 mu g m- 3 at Mohal and 1.1 f 1.4 mu g m-3 at Katarmal. BC showed strong seasonal variability, with maxima during post-monsoon (2.6 f 1.0 mu g m- 3) and pre-monsoon (1.8 f 0.5 mu g m-3) seasons. The diurnal variation displayed distinct morning and evening peaks in all the seasons. High pre-monsoon AOD500 (0.30 f 0.06 to 0.54 f 0.08) and low values of & Aring;ngstrom exponent (0.67 f 0.10 to 0.95 f 0.30) indicated dominance of large particles, whereas lower AOD500 (0.21 f 0.07 to 0.25 f 0.03) in post-monsoon and winter, along with larger & Aring;ngstrom exponent (1.05 f 0.74 to 1.13 f 0.11), indicated smaller particles. Satellite-derived (OMI and MAIAC) AOD500 showed weak to moderate correlation with ground-based measurements at Mohal (R = 0.4639 for MAIAC, R = 0.1402 for OMI) and Katarmal (R = 0.3976 for MAIAC, R = 0.2980 for OMI). Using optical properties of aerosols and clouds (OPAC) and Santa Barbara discrete ordinate radiative transfer (SBDART) models, the short-wave aerosol radiative forcing (SWARF) was found negative at the surface and top of the atmosphere but positive in the atmosphere, suggesting significant surface cooling and atmospheric warming leading to high heating rates, respectively. Annual mean atmospheric radiative forcing was 27.36 f 6.00 Wm- 2 at Mohal and 21.87 f 7.26 Wm- 2 at Katarmal. These findings may have consequences for planning air pollution strategies and understanding the effects of regional climate change.

In South Asia, our understanding of atmospheric aerosols and their optical properties is limited, posing a challenge to comprehending climate change dynamics. This study characterises aerosol optical properties, radiative properties, black carbon (BC) and ozone (O3) at seven South Asian locations, including Nam Co (Tibetan Plateau, TP), Dhaka, Bhola (Bangladesh), and Hanimaadhoo, Kashidhoo, Male' and Gan (Maldives). The study utilises columnar aerosol data from the Aerosol Robotic Network (AERONET) and reanalysis data from Modern-Era Retrospective Analysis for Research and Applications (MERRA-2) from 2001 to 2020. Notably, during the winter, the highest Aerosol optical depth (AOD) levels were observed in Dhaka (1.0 +/- 0.5) and Bhola (0.8 +/- 0.4) among these seven locations. BC concentrations in Dhaka ranged from 2.1 to 2.8 mu g m-3, while Bhola recorded concentrations between 1.4 and 2.1 mu g m-3. O3 levels across Maldives sites remained consistent, with values ranging between 314 and 345 dobson units (DU), surpassing those in Bangladesh and TP. The analysis shows a significant difference in the rate at which the atmosphere heats (HR) up due to aerosols. Higher heating rates were observed over Kashidhoo during the post-monsoon and winter seasons, while lower values were seen during the pre-monsoon and monsoon seasons, compared with Hanimaadhoo and Male'. It is important to note that Bangladesh had higher HR values than the Maldives. This study helps us better understand the impact of atmospheric aerosols on South Asia's climate and the different seasonal patterns.

Refractory black carbon (rBC) is a primary aerosol species, produced through incomplete combustion, that absorbs sunlight and contributes to positive radiative forcing. The overall climate effect of rBC depends on its spatial distribution and atmospheric lifetime, both of which are impacted by the efficiency with which rBC is transported or removed by convective systems. These processes are poorly constrained by observations. It is especially interesting to investigate rBC transport efficiency through the Asian Summer Monsoon (ASM) since this meteorological pattern delivers vast quantities of boundary layer air from Asia, where rBC emissions are high to the upper troposphere/lower stratosphere (UT/LS) where the lifetime of rBC is expected to be long. Here, we present in situ observations of rBC made during the Asian Summer Monsoon Chemistry and Climate Impact Project of summer, 2022. We use observed relationships between rBC and CO in ASM outflow to show that rBC is removed nearly completely (>98%) from uplifted air and that rBC concentrations in ASM outflow are statistically indistinguishable from the UT/LS background. We compare observed rBC and CO concentrations to those expected based on two chemical transport models and find that the models reproduce CO to within a factor of 2 at all altitudes whereas rBC is overpredicted by a factor of 20-100 at altitudes associated with ASM outflow. We find that the rBC particles in recently convected air have thinner coatings than those found in the UTLS background, suggesting transport of a small number of rBC particles that are negligible for concentration.

In this study, we used satellite observations to identify 10 typical dust-loading events over the Indian Himalayas. Next, the aerosol microphysical and optical properties during these identified dust storms are characterized using cotemporal in situ measurements over Mukteshwar, a representative site in Indian Himalayas. Relative to the background values, the mass of coarse particles (size range between 2.5 and 10 mu m) and the extinction coefficient were found to be enhanced by 400% (from 24 +/- 15 to 98 +/- 40 mu g/m3) and 175% (from 89 +/- 57 Mm-1 to 156 +/- 79 Mm-1), respectively, during these premonsoonal dust-loading events. Moreover, based on the air mass trajectory, these dust storms can be categorized into two categories: (a) mineral dust events (MDEs), which involve long-range transported dust plumes traversing through the lower troposphere to reach the Himalayas and (b) polluted dust events (PDEs), which involve short-range transported dust plumes originating from the arid western regions of the Indian subcontinent and traveling within the heavily polluted boundary layer of the Gangetic plains before reaching the Himalayas. Interestingly, compared to the background, the SSA and AAE decrease during PDEs but increase during MDEs. More importantly, we observe a twofold increase in black carbon concentrations and the aerosol absorption coefficient (relative to the background values) during the PDEs with negligible changes during MDEs. Consequently, the aerosol-induced snow albedo reduction (SAR) also doubles during MDEs and PDEs relative to background conditions. Thus, our findings provide robust observational evidence of substantial dust-induced snow and glacier melting over the Himalayas.