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.

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.

Atmospheric particulate matter (PM) as light-absorbing particles (LAPs) deposited to snow cover can result in early onset and rapid snow melting, challenging management of downstream water resources. We identified LAPs in 38 snow samples (water years 2013-2016) from the mountainous Upper Colorado River basin by comparing among laboratory-measured spectral reflectance, chemical, physical, and magnetic properties. Dust sample reflectance, averaged over the wavelength range of 0.35-2.50 mu m, varied by a factor of 1.9 (range, 0.2300-0.4444) and was suppressed mainly by three components: (a) carbonaceous matter measured as total organic carbon (1.6-22.5 wt. %) including inferred black carbon, natural organic matter, and carbon-based synthetic, black road-tire-wear particles, (b) dark rock and mineral particles, indicated by amounts of magnetite (0.11-0.37 wt. %) as their proxy, and (c) ferric oxide minerals identified by reflectance spectroscopy and magnetic properties. Fundamental compositional differences were associated with different iron oxide groups defined by dominant hematite, goethite, or magnetite. These differences in iron oxide mineralogy are attributed to temporally varying source-area contributions implying strong interannual changes in regional source behavior, dust-storm frequency, and (or) transport tracks. Observations of dust-storm activity in the western U.S. and particle-size averages for all samples (median, 25 mu m) indicated that regional dust from deserts dominated mineral-dust masses. Fugitive contaminants, nevertheless, contributed important amounts of LAPs from many types of anthropogenic sources.

This work uses a mixture of observations from surface remote sensing (AERONET) and satellite remote sensing (OMI) to uniquely compute the atmospheric column loading of black carbon (BC) mass concentration density (MCD) and number concentration density (NCD) on a grid-by-grid, day-by-day basis at 0.25 degrees x0.25 degrees over rapidly developing and biomass burning (BB) impacted regions in South, Southeast, and East Asia. This mixture of observations is uniformly analyzed based on OMI NO2 retrievals, OMI Near ultraviolet band absorption aerosol optical depth and single scattering albedo (SSA), and AERONET visible and near-infrared band SSA observations, in connection with an inversely applied MIE mixing model approach. This method uniquely solves for the unbiased spatial and temporal domains based on variance maximization of daily NO2. These locations in space and time are then used to quantify the distribution of all possible individual particle core and refractory shell sizes as constrained by all band-by-band observations of SSA from AERONET. Finally, the range of NCD and MCD are computed from the constrained range of per-particle core and refractory shell size on a grid-by-grid and day-byday basis. The maps of MCD and NCD are consistent in space and time with known urban, industrial, and BB sources. The statistical distributions are found to be non-normal, with the region-wide mean, 25th, 50th, and 75th percentile MCD [mg/m2] of 90.3, 56.1, 81.1, and 111 respectively, and NCD [x1012 particles/m2] of 8.76, 4.63, 7.39, and 11.3 respectively. On a grid-by-grid basis, a significant amount of variation is found, particularly over Myanmar, Laos, northern Thailand, and Vietnam, with this subregional mean, 25th, 50th, and 75th MCD [mg/m2] of 90.7, 56.1, 81.3, and 112 respectively and NCD [x1012 particles/m2] of 9.66, 5.49, 8.33, and 12.3 respectively. On a day-to-day basis, events are determined 121 days in 2016, during which the computed statistics of MCD and NCD have mean and uncertainty ranges which scale with each other. However, there are 11 days where the uncertainty ratio of NCD values is larger than 1 while the uncertainty ratio of MCD is small, and 5 days where the reverse is observed, indicating that the particle size is strongly atypical on these days, consistent with mixed aerosol sources, a substantial change in the aerosol aging, or other such factors including a substantial region of overlap between BB and urban sources. The high values observed from March to May lead to an extended BB season as compared to previous work focusing on fire radiative power, NO2, and models, which show a shorter season (usually ending in early April). The results are consistent with BC being able to transport significant distances. The new approach is anticipated to provide support for improving radiative forcing calculations, estimating emissions inventories, and providing a basis by which models can compare against observations.

Black carbon (BC) is one of the major aerosol components with relatively high implications on climatic patterns through its radiative forcing (RF). South Asia has recently experienced an increased concentration of pollution; however, relatively fewer studies have been carried out on long-term assessment of BC and its implications. The present study analyzed the long-term concentration of BC in selected urban locations over South Asia using the Modern-Era Retrospective analysis for Research and Applications, version 2 (MERRA-2). The study employed statistical analysis, including linear regression techniques, to assess the long-term concentration of BC. The results show that a rapid increase of BC is observed over most urban locations of South Asia with the predominance in winter and hence requires strict regional control measures to reduce the excess concentration of BC in the atmosphere. High concentration of BC in winter is attributed to anthropogenic activities and changes in meteorological conditions that enhance the accumulation of pollutants in the atmosphere. The relationship of BC with cloud top temperature and cloud effective radius demonstrates the direct and indirect effect of BC on cloud properties in this region. The RF results reveal that aerosol optical depth has positive aerosol RF in the atmosphere and negative RF at the top of the atmosphere (TOA) as well as at the bottom of the atmosphere (BOA). Negative RF at the TOA indicates less forcing efficiency due to fewer BC aerosols. On the other hand, averaging aerosol RF within the atmosphere reveals positive forcing, which suggests the efficiency force exerted by BC aerosols after absorbing solar radiation.

The significant uncertainties of Black Carbon (BC) radiative forcing are becoming an obstacle to the evaluation of their impacts and mitigation measures. One of the crucial reasons for this uncertainty could be the poorly constrained BC vertical profile. The BC has a lifetime of a few days to weeks and there is a clear pointer that it can be vertically transported through convection besides the horizontal advection. The present study aims for the intercomparison between the BC mass concentrations obtained through the aircraft-based observations and that derived from the selected Copernicus Atmosphere Monitoring Service (CAMS) reanalysis data over the three different locations of India, which is one of the largest emitters of BC aerosols. The aircraft-based BC observations were conducted from 0.5 to 7 km altitudes using Aethalometer during CAIPEEX (Cloud Aerosol Interaction and Precipitation Enhancement Experiment) Phase I campaigns from June to September 2009. The output of the present study suggests the CAMS reanalysis data significantly underestimated BC mass throughout the vertical profile with an average mass normalized mean bias of greater than -70% at all three locations. Furthermore, the vertical radiative forcing and heating rates of BC were also calculated for both observation and reanalysis data. The output depicts the net forcing due to CAMS simulated BC in all the layers were 1-12 folds lower over all the study regions compared with observed BC aerosols. Likewise, the estimated mean biases in heating rate were in the range of -0.001 to -0.190 K day(-1) for all the vertical layers over the study locations. The possible reasons for these disparities could be poorly constrained emissions, especially aircraft emissions and/or their transformation schemes in aerosol modules. The present study emphasized that the validation of the vertical profile is also an essential factor for better constraints of the BC aerosols in climate models.

Black carbon is a short-lived climate warming agent and serves as a crucial factor influencing the climate. Numerous models, observations, and laboratory studies have been conducted to quantify black carbon's direct or indirect impacts on the climate. Here, we applied bibliometric analysis to identify research trends and key topics on black carbon in the climate field. Based on the Web of Science (WOS) Core Collection database, a total of 4903 documents spanning the period from 2000 to 2023 were retrieved and screened, focusing on the topic of black carbon in the climate field, resulting in the Black-Carbon Climate Local (BCL) dataset. Our study examines the influence and trends of major countries, institutions, and authors in this field. The results show that China and the United States hold leading positions in terms of the number of publications. Based on keyword networks, the BCL dataset is segmented into six distinct research directions, and representative keywords of each direction include biomass burning, radiative forcing, air pollution, aerosol optical depth, optical properties, and biochar. This study helps to identify the current research status and trends of black carbon in the climate, highlighting main research directions and emerging topics.

In this study, we investigated the aerosol radiative forcing (ARF) using ground-based measurements of PM2.5 and black carbon aerosols at a semi-arid, rain shadow location, Solapur in peninsular India. It is observed that aerosols caused a net cooling effect at top of the atmosphere (TOP) indicating that the aerosols reflect more solar radiation back to space than they absorb. At the surface, the aerosols caused a net cooling effect indicating more presence of scattering type aerosols. The resulting ARF of the aerosols was found to be ranging from +38 Wm-2 in monsoon to +53 Wm-2 in pre-monsoon indicating trapping of energy which resulted in a warming of the atmosphere. However, BC -only forcing indicated a significant warming effect at TOP as well as in the atmosphere which showed the potential of the absorbing carbonaceous aerosols. Overall, BC was responsible for 44% and 32% of the composite ARF, even though it formed only 7% and 2% of composite aerosol in the dry and wet periods, respectively. The warming impact of BC aerosols was also manifested in terms of their contribution to aerosol radiative forcing efficiency (ARFE) which was about four times more for BC-only than that for composite aerosols. More atmospheric heating rates were observed during dry periods for composite and BC-only aerosols than during wet period. These findings have important implications for aerosol-cloud-precipitation studies as well as the atmospheric thermodynamics and hydrological cycle over this semi-arid region where the total aerosol load is not significant and rainfall amount is scarce.

Light-absorbing carbonaceous aerosols that dominate atmospheric aerosol warming over India remain poorly characterized. Here, we delve into UV-visible-IR spectral aerosol absorption properties at nine PAN-India COALESCE network sites (Venkataraman et al., 2020, ). Absorption properties were estimated from aerosol-laden polytetrafluoroethylene filters using a well-constrained technique incorporating filter-to-particle correction factors. The measurements revealed spatiotemporal heterogeneity in spectral intrinsic and extrinsic absorption properties. Absorption analysis at near-UV wavelengths from carbonaceous aerosols at these regional sites revealed large near-ultraviolet brown carbon absorption contributions from 21% to 68%-emphasizing the need to include these particles in climate models. Further, satellite-retrieved column-integrated absorption was dominated by surface absorption, which opens possibilities of using satellite measurements to model surface-layer optical properties (limited to specific sites) at a higher spatial resolution. Both the satellite-modeled and direct in-situ absorption measurements can aid in validating and constraining climate modeling efforts that suffer from absorption underestimations and high uncertainties in radiative forcing estimates. Particulate pollution in the atmosphere scatter and absorb incoming solar energy, thus cooling or warming Earth's atmosphere. In developing countries and especially in India, one of the most polluted regions of the world, the extent to which particles can absorb solar energy and warm the atmosphere is not well understood. Here, for the first time, we measure particle absorption simultaneously at nine ground sites across India, in diverse geographical regions with different levels and types of particulate pollution. We find that organic carbon particles exert large absorption at near-ultraviolet wavelengths, which contain significant solar energy. These light absorbing organic carbon particles, called brown carbon, are emitted in large quantities from biomass burning (e.g., burning crop residue and cooking on wood-fired stoves). Comparing ground measurements of absorption with satellite-retrieved measurements that are representative of the entire atmospheric column, we find that near-surface atmospheric particles can exert significant warming. This study highlights the need to improve climate model simulations of particulate pollution's impact on the climate by incorporating spatiotemporal surface-level absorption measurements, including absorption by brown carbon particles. Measurements at nine regional PAN-India sites reveal several regions with large aerosol absorption strength Brown carbon contributes significantly (21%-68%) to near-ultraviolet absorption, indicating its importance in shortwave light absorption Strong correlations observed between satellite data and surface absorption indicate future potential in modeling surface absorption