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.

Carbonaceous aerosol, including organic carbon (OC) and elemental carbon (EC), has significant influence on human health, air quality and climate change. Accurate measurement of carbonaceous aerosol is essential to reduce the uncertainty of radiative forcing estimation and source apportionment. The accurate separation of OC and EC is controversial due to the charring of OC. Therefore, the development of reference materials (RM) for the validation of OC/EC separation is an important basis for further study. Previous RMs were mainly based on ambient air sampling, which could not provide traceability of OC and EC concentration. To develop traceable RMs with known OC/EC contents, our study applied an improved aerosol generation and mixing technique, providing uniform deposition of particles on quartz filters. To generate OC aerosol with similar pyrolytic property of ambient aerosol, both water soluble organic carbon (WSOC) and water insoluble organic carbon (WIOC) were used, and amorphous carbon was selected for EC surrogate. The RMs were analyzed using different protocols. The homogeneity within the filter was validated, reaching below 2%. The long -term stability of RMs has been validated with RSD ranged from 1.7%-3.2%. Good correlation was observed between nominal concentration of RMs with measured concentration by two protocols, while the difference of EC concentration was within 20%. The results indicated that the newly developed RMs were acceptable for the calibration of OC and EC, which could improve the accuracy of carbonaceous aerosol measurement. Moreover, the laboratory-generated EC-RMs could be suitable for the calibration of equivalent BC concentration by Aethalometers. (c) 2024 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )

Aerosols are an important factor leading to reduced visibility. In order to better comprehend the connection between visibility and aerosols, aerosol optical depth (AOD) and Angstrom exponent (AE) data from the Himawari-8 Advanced Himawari Imager (AHI) are used for validation in comparison with the data from the Aerosol Robotic Network (AERONET) observations in this paper, which amounted to 69,026 sets of data. The results indicate that the AOD of AHI is in good agreement with AERONET observations, but AE performs poorly. The correlation coefficients between the AOD of AHI and AERONET data increase with decreasing visibility and the root mean square error increase. The AE of AHI performs poorly in different visibility conditions. The conclusion drawn from further analysis of the correlation between aerosol products and meteorological factors is that the factor with the highest correlation with visibility. Mixed aerosols dominate at higher visibility and biomass burning/urban-industrial aerosols dominate at lower visibility. The visibility in a typical city (Beijing) has a strong negative correlation with AOD, a weak negative correlation with AE, and a strong correlation with aerosol radiative forcing. The reduction in visibility may be caused by the scattering and adsorption effects of aerosols. The results are important for the improvement and application of AHI aerosol products in regional pollution studies.

Under environment with various water contents, the variations in the mixing state and particle size of coated black carbon (BC) aerosols cause changes in optical and radiative effects. In this study, fractal models for thinly, partially, and thickly coated BC under six relative humidities (RHs 1/4 0-95%) are constructed and optically simulated at 1064 and 532 nm. Differential scattering cross-sections are selected to retrieve the mixing state (Dp/Dc) of BC to investigate the possible retrieval errors caused by the nonspherical morphology when using the single-particle soot photometer (SP2). Furthermore, the radiative forcing of BC aerosols at different RHs are analyzed. Results showed that the retrieval errors (REs) of Dp/Dc are negative for coated particles with BC volume fraction smaller than 0.10, indicating that the mixing states of coated fractal BC are underestimated during the hygroscopic growth. The partiallycoated BC has the best retrieval accuracy of the mixing state, followed by the closed-cell and coatedaggregate model, judging from averaged REs. Radiative forcing enhancements for partially-coated aerosols with different BC volume fractions exponentially increase to opposite values, resulting in a warming or cooling effect. This study helps understand the uncertainties in Dp/Dcof BC aerosols retrieved by SP2 and their radiative forcing at different RHs. (c) 2025 Chinese Society of Particuology and Institute of Process Engineering, Chinese Academy of Sciences. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.

Pollutant emissions in China have significantly decreased over the past decade and are expected to continue declining in the future. Aerosols, as important pollutants and short-lived climate forcing agents, have significant but currently unclear climate impacts in East Asia as their concentrations decrease until mid-century. Here, we employ a well-developed regional climate model RegCM4 combined with future pollutant emission inventories, which are more representative of China to investigate changes in the concentrations and climate effects of major anthropogenic aerosols in East Asia under six different emission reduction scenarios (1.5 degrees C goals, Neutral-goals, 2 degrees C -goals, NDC-goals, Current-goals, and Baseline). By the 2060s, aerosol surface concentrations under these scenarios are projected to decrease by 89%, 87%, 84%, 73%, 65%, and 21%, respectively, compared with those in 2010-2020. Aerosol climate effect changes are associated with its loadings but not in a linear manner. The average effective radiative forcing at the surface in East Asia induced by aerosol-radiation-cloud interactions will diminish by 24% +/- 13% by the 2030s and 35% +/- 13% by the 2060s. These alternations caused by aerosol reductions lead to increases in near-surface temperatures and precipitations. Specifically, aerosol-induced temperature and precipitation responses in East Asia are estimated to change by -78% to -20% and -69% to 77%, respectively, under goals with different emission scenarios in the 2060s compared to 2010-2020. Therefore, the significant climate effects resulting from substantial reductions in anthropogenic aerosols need to be fully considered in the pathway toward carbon neutrality.

Aerosols can alter atmospheric stability through radiative forcing, thereby changing mean and daily extreme precipitation on regional scales. However, it is unclear how extreme sub-daily precipitation responds to aerosol radiative effects. In this study, we use the regional climate model (RCM) Consortium for Small-scale Modeling (COSMO) to perform convection-permitting climate simulations at a kilometer-scale (0.04 degrees/similar to 4.4 km) resolution for the period 2001-2010. By evaluating against the observed hourly precipitation-gauge data, the COSMO model with explicit deep convection can effectively reproduce sub-daily and daily extreme precipitation events, as well as diurnal cycles of summer mean precipitation and wet hour frequency. Moreover, aerosol sensitivity simulations are conducted with sulfate and black carbon aerosol perturbations to assess the direct and semi-direct aerosol effects on extreme sub-daily precipitation in the COSMO model. The destabilizing effects associated with decreased sulfate aerosols intensify extreme sub-daily precipitation, while increased sulfate aerosols tend to induce an opposite change. In contrast, the response of extreme sub-daily precipitation to black carbon aerosol perturbations exhibits a nonlinear behavior and potentially relies on geographical location. Overall, the scaling rates of extreme precipitation intensities decrease and approach the Clausius-Clapeyron rate from hourly to daily time scales, and the responses to sulfate and black carbon aerosols vary with precipitation durations. This study improves the understanding of aerosol radiative effects on sub-daily extreme precipitation events in RCMs.

Brown carbon (BrC) has been recognized as an important light-absorbing carbonaceous aerosol, yet understanding of its influence on regional climate and air quality has been lacking, mainly due to the ignorance of regional coupled meteorology-chemistry models. Besides, assumptions about its emissions in previous explorations might cause large uncertainties in estimates. Here, we implemented a BrC module into the WRF-Chem model that considers source-dependent absorption and avoids uncertainties caused by assumptions about emission intensities. To our best knowledge, we made the first effort to consider BrC in a regional coupled model. We then applied the developed model to explore the impacts of BrC absorption on radiative forcing, regional climate, and air quality in East Asia. We found notable increases in aerosol absorption optical depth (AAOD) in areas with high OC concentrations. The most intense forcing of BrC absorption occurs in autumn over Southeast Asia, and values could reach around 4 W m(-2). The intensified atmospheric absorption modified surface energy balance, resulting in subsequent declines in surface temperature, heat flux, boundary layer height, and turbulence exchanging rates. These changes in meteorological variables additionally modified near-surface dispersion and photochemical conditions, leading to changes of PM2.5 and O-3 concentrations. These findings indicate that BrC could exert important influence in specific regions and time periods. A more in-depth understanding could be achieved later with the developed model.

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.

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.

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