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Satellite-based aerosol optical depth (AOD) is columnar light extinction by aerosol absorption and scattering and has become the most important variable for the assessment of the spatiotemporal distribution of aerosols at a regional and global level. In this paper, we have used AOD observations of multiangle imaging spectroradiometer (MISR) from September 2002 to May 2017, moderate resolution imaging spectroradiometer (MODIS) from September 2002 to December 2020, and sea-viewing wide field-of-view sensor (SeaWiFS) from September 2002 to December 2010 over South Asia. We have observed the association of AOD with enhanced vegetation index (EVI) and meteorological variables (temperature (TEMP), wind speed (WS), and relative humidity (RH)) acquired from Giovanni during the period September 2002–December 2020. The satellite observations of Terra-, MISR-, and SeaWiFS-AOD were also compared with Aqua-AOD. The findings show that AOD in eastern Pakistan is higher than in the western Pakistan due to increase in population density and biomass burning. Mean annual peak AOD (˃ 0.7) has been observed over the IGB region because of the significant increase in economical, industrial, and agricultural activities while AOD of ˃ 0.6 is observed over Bangladesh. The lowest mean annual AOD of ˂ 0.3 is observed over northeastern Afghanistan, western Nepal, and Bhutan whereas the AOD of 0.3 is seen over Sri Lanka. The highest seasonal mean AOD of 0.8 has been seen over Bihar, India, and AOD of ~ 0.7 is observed over Bangladesh while the lowest AOD is observed over Afghanistan, Sri Lanka, Nepal, and Bhutan during the winter season. However, the mean AOD over eastern Pakistan is maximum in both monsoon and post-monsoon season but relatively low in pre-monsoon and winter. The highest positive seasonal AOD anomalies were observed over South Asia in winter season followed by post-monsoon, pre-monsoon, and least being monsoon. The higher mean AOD anomaly value is found to be 0.2 over eastern Pakistan and western India. In northeastern Pakistan and central India, AOD and RH are positively correlated (r ˃ 0.54) while negatively correlated over Afghanistan, southwestern region of Pakistan, eastern India, Nepal, Bhutan, and Bangladesh. AOD is negatively correlated (r = ~ − 0.3) with EVI over eastern Pakistan and western India. The highest correlation coefficient (r) obtained among Terra and Aqua is 0.97, MISR and Aqua is 0.93, and SeaWiFS and Aqua is 0.58 over South Asia. [ABSTRACT FROM AUTHOR]

South Asian air pollutants exert substantial effect on the climate and environment change over the Tibetan Plateau (TP). This paper investigates the trans-boundary transport of PM 10 , PM 2.5 , and O 3 from South Asia to the TP via WRF-Chem sensitive analysis. It is found that PM 10 , PM 2.5 , and O 3 over South Asia are mainly sourced from anthropogenic sources. South Asian emissions contribute up to 54% of PM 10 (PM 2.5) in the TP in the pre-monsoon season. For O 3 , the highest contribution of 18.13% is in the monsoon season, while the lowest contribution of 8.67% is in the winter season. To evaluate the respective contributions of anthropogenic and biomass burning emissions in South Asia to PM 10 , PM 2.5 , and O 3 in the TP, anthropogenic and biomass burning emissions in South Asia are considered separately. The results show that the largest percentage contribution of PM 10 (PM 2.5) from South Asian anthropogenic emissions to PM 10 (PM 2.5) in the TP with value of 35.86% (37.77%) occurs in winter, while the lowest percentage contribution of 16.52% (16.77%) appears in the monsoon season. For O 3 , the largest contribution of 17.74% from South Asian anthropogenic emissions appears in the monsoon season, whereas the lowest contribution of 8.59% occurs in winter. Compared to the anthropogenic emissions, the biomass burning emissions in South Asia have a relative less contribution to PM 10 , PM 2.5 , and O 3 in the TP. The largest contribution of PM 10 (PM 2.5) from South Asian biomass burning emissions to PM 10 (PM 2.5) in the TP is 20.04% (18.37%) in the pre-monsoon season. Conversely, the lowest contribution of 0.58% (0.53) appears in the monsoon season. O 3 from South Asian biomass burning emissions contributes <1% to O 3 in the TP in each season, implying that the biomass burning emissions in South Asia have little effect on O 3 in the TP. This study is of great significance to the ecological environment protection for the TP. • Contributions of South Asian emissions to PM 10 , PM 2.5 , and O 3 in the TP are quantified. • Anthropogenic emissions in South Asia have a larger contribution to PM 10 , PM 2.5 , and O 3 in the TP. • O 3 from South Asian biomass burning emissions contributes <1% to O 3 in the Tibetan Plateau. [ABSTRACT FROM AUTHOR]

Aerosol particles with diameters larger than 40 nm were collected during the flight campaign StratoClim 2017 within the Asian tropopause aerosol layer (ATAL) of the 2017 monsoon anticyclone above the Indian subcontinent. A multi-impactor system was installed on board the aircraft M-55 Geophysica, which was operated from Kathmandu, Nepal. The size and chemical composition of more than 5000 refractory particles/inclusions of 17 selected particle samples from seven different flights were analyzed by use of scanning electron microscopy (SEM) and transmission electron microscopy (TEM) combined with energy dispersive X-ray (EDX) microanalysis. Based on chemical composition and morphology, the refractory particles were assigned to the following particle groups: extraterrestrial, silicates, Fe-rich, Al-rich, Hg-rich, other metals, C-rich, soot, Cl-rich, and Ca-rich. Most abundant particle groups within the refractory particles are silicates and C-rich (non-volatile organics). In samples taken above the tropopause, extraterrestrial particles are becoming increasingly important with rising altitude. The most frequent particle sources for the small (maximum in size distribution DP-max=120 nm) refractory particles carried into the ATAL are combustion processes at the ground (burning of fossil fuels/biomass burning) and the agitation of soil material. The refractory particles in the ATAL represent only a very small fraction (< 2 % by number for particles > 40 nm) of the total aerosol particles, which are dominated by species like ammonium, sulfate, nitrate, and volatile organics. During one flight, a large number of very small (DP-max=25 nm) cinnabar particles (HgS) were detected, which are supposed to originate from a ground source such as coal combustion or underground coal fires. [ABSTRACT FROM AUTHOR]

Over the past few decades, the tropospheric ozone precursor anthropogenic emissions: nitrogen oxides (NOx) and reactive carbon (RC) from mid-latitude regions have been decreasing, and those from Asia and tropical regions have been increasing, leading to an equatorward emission redistribution. In this study, we quantify the contributions of various sources of NOx and RC emissions to tropospheric ozone using a source attribution technique during the 2000–2018 period in a global chemistry transport model: CAM4-Chem. We tag the ozone molecules with the source of their NOx or RC precursor emission in two separate simulations, one for each of NOx and RC. These tags include various natural (biogenic, biomass burning, lightning and methane), and regional anthropogenic (North American, European, East Asian, South Asian etc.) precursor emission sources. We simulate ~336 Tg O3 with an increasing trend of 0.91 Tg O3/yr (0.28 %/yr), largely contributed (and trend driven) by anthropogenic NOx emissions and methane. The ozone production efficiency of regional anthropogenic NOx emissions increases significantly when emissions decrease (Europe, North American and Russia-Belarus-Ukraine region's emissions) and decreases significantly when emissions increase (South Asian, Middle Eastern, International Shipping etc.). Tropical regions, despite smaller emissions, contribute more to tropospheric ozone burden compared to emissions from higher latitudes, consistent with previous work, due to large convection at the tropics thereby lifting O3 and its precursor NOx molecules into the free troposphere where ozone's lifetime is longer. We contrast the contribution to tropospheric ozone burden with that of the contribution to the global surface ozone. We simulate a smaller relative contribution from tropical regions to the global mean surface ozone compared to their contribution to the tropospheric ozone burden. The global population-weighted mean ozone (related to ozone exposure) is much larger compared to surface mean, mainly due to large anthropogenic emissions from densely populated regions: East Asia, South Asia, and other tropical regions, and a substantial contribution from international ship NOx emissions. The increasing trends in anthropogenic emissions from these regions are the main drivers of increasing global population-weighted mean ozone. [ABSTRACT FROM AUTHOR]

This study estimates the radiative forcing by biomass burning and dust aerosols over the Indian subcontinent, with emphasis on the Indo-Gangetic Plains (IGP) during the period from January 2021 to April 2021, based on multiple satellite and reanalysis datasets. In this respect, we used retrievals from the Moderate Resolution Spectroradiometer (MODIS) and the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) system, as well as reanalysis data from the Goddard Earth Observing System, version 5 (GEOS-5), the Modern-Era Retrospective analysis for Research and Applications, version 2 (MERRA-2), the Copernicus Atmosphere Monitoring Service (CAMS), and ERA-Interim. According to the MERRA-2 and the CAMS, the highest black carbon (BC) concentrations in January 2021 were 7–8 µg m−3, which were significantly lower than measurements performed in main cities along the IGP, such as Patiala, Delhi, and Kanpur. The meteorological data analysis accompanied by the CALIPSO lidar measurements showed that the vertical distribution of total attenuated backscatter (TAB) could reach altitudes of up to ~4–5 km and could be transported over the central Himalayan region. The spatial-averaged daily aerosol radiative forcing (ARF) values over the Indian subcontinent from January 2021 to April 2021 were found to range from −51.40 to −6.08 W m−2 (mean of −22.02 ± 9.19 W m−2), while on a monthly basis, the ARF values varied widely, from −146.24 to −1.63 W m−2 (mean of −45.56 ± 22.85 W m−2) over different parts of the study region. Furthermore, the spatial-averaged daily BC radiative forcing ranged from −2.23 to −0.35 (−1.01 ± 0.40 W m−2), while it varied from −15.29 to −0.31 W m−2 (−2.46 ± 2.32 W m−2) over different regions of southern Asia, indicating a rather small contribution to the total aerosol radiative effect and a large presence of highly scattering aerosols. Our findings highlight the importance of growing biomass burning, in light of recent climate change and the rapid decline in air quality over North India and the Indian Ocean. [ABSTRACT FROM AUTHOR]

Devising effective national-level climate action plans needs a more detailed understanding of the regional distribution of sources and sinks of greenhouse gases. Due to insufficient observations and modelling capabilities, India's current carbon source-sink estimates are uncertain. This study uses a high-resolution transport model to examine the potential of CO2 observations over India for inverse estimation of regional carbon fluxes. We make use of four different sites in India that vary in measurement technique, frequency and spatial representation. These observations exhibit substantial seasonal (7.5 to 9.2 ppm) and intra-seasonal (2 to 12 ppm) variability. Our modelling approach, a high-resolution Weather Research and Forecasting Model combined with Stochastic Time Inverted Lagrangian Transport (WRF-STILT) model, performs better in simulating seasonal (R2 = 0.50 to 0.96) and diurnal (R2 = 0.96) variability of observed CO2 than the current generation global models analysed in the study. Representation of local flux variability like biomass burning in the model needs further refinement, depending on the site location. During the agricultural season, crop biospheric uptake in the Indo-Gangetic Plain region significantly modulates the CO2 variability in the northern Indian stations. Depending on the region and time of the year, the anthropogenic and biospheric emission components contribute differently to CO2 variability. The choice of emission inventory in the modelling framework alone leads to significant biases in simulations (5 to 10 ppm), endorsing the need for accounting emission fluxes, especially for non-background sites. By implementing a high-resolution model, our results emphasise that observations from Indian sites can be useful in deducing carbon flux information at regional (Nainital) and sub-urban to urban (Mohali, Shadnagar, Nagpur) scales. On accounting for observed variability, the global carbon data assimilation system can thus benefit from the measurements from the Indian subcontinent. [ABSTRACT FROM AUTHOR]

Light-absorbing Brown Carbon (BrC) aerosols partially offset the overall climate-cooling of aerosols. However, the evolution of BrC light-absorption during atmospheric transport is poorly constrained. Here, we utilize optical properties, ageing-diagnostic δ13C-BrC and transport time to deduce that the mass absorption cross-section (MACWS-BrC) is decreasing by ~50% during long-range oversea transport, resulting in a first-order bleaching rate of 0.24 day‒1 during the 3-day transit from continental East Asia to a south-east Yellow Sea receptor. A modern 14C signal points to a strong inverse correlation between BrC light-absorption and age of the source material. Combining this with results for South Asia reveals a striking agreement between these two major-emission regions of rapid photobleaching of BrC with a higher intrinsic absorptivity for BrC stemming from biomass burning. The consistency of bleaching parameters constrained independently for the outflows of both East and South Asia indicates that the weakening of BrC light absorption, thus primarily related to photochemical processes rather than sources, is likely a ubiquitous phenomenon. [ABSTRACT FROM AUTHOR]

Daytime and nighttime PM10 samples were collected during summer (June) and winter (February) at a representative urban site in Mumbai, located on the western coast of Indian subcontinent. Samples were studied for molecular distribution of water-soluble dicarboxylic acids, oxoacids and dicarbonyls as well as total carbon (TC), water-soluble organic carbon (WSOC), inorganic ions along with specific markers (levoglucosan, K+) to better understand sources and formation processes of organic aerosols in Mumbai. The distribution of water-soluble organics was characterised by high abundance of oxalic acid (C2), followed by phthalic (Ph), terephthalic (tPh), azelaic (C9), malonic (C3), and succinic acids (C4). Positive correlations between C2, sulfate and glyoxal (ωC2) suggest secondary production of C2 predominantly via aqueous phase chemistry. C2 also showed positive correlation with K+ and levoglucosan indicating that biomass/biofuel burning is the potential source of diacids in the Mumbai aerosols. In addition, higher average contributions of total diacids to WSOC and OC in winter than in summer suggest that aerosols were aged i.e., photochemically well processed in winter in Mumbai. On the other hand, diurnal change in their ratios is observed with higher ratio in daytime samples than that of previous and succeeding nighttime samples, suggesting diacids are also influenced from local sources in both the seasons. This study demonstrates that biomass burning as well as biogenic sources are important sources influencing the distributions of aerosols in Mumbai. [ABSTRACT FROM AUTHOR]

Known as the "third pole" and "water tower of Asia", the Tibetan Plateau (TP) is the home to the largest number of glaciers in the mid-latitudes and one of the most sensitive areas to global climate change due to its special geographical location and powerful thermodynamic effects. In recent years, the TP has been affected by exogenous pollutants and the concentrations of some pollutants have shown an increasing trend, especially light-absorbing aerosols (LAAs), when ice core records, ground- and aircraft-based field campaigns and satellite technology enabled synthesized monitoring. The enhanced warming of the vast majority of regions in TP, together with Arctic warming, and snow/ice decline, represents credible evidence of anthropogenic climate change. This paper provides a comprehensive review of studies on the sources, characteristics and climate impacts of LAAs over the TP. Adjacent to the two major emission sources of LAAs in East Asia and South Asia, the unique geographical location and climatic characteristics of the TP make it possible for TP LAAs to cause atmospheric warming and accelerated glacier melting, affecting the hydrological cycle in South Asia, East Asia and even the Northern Hemisphere, thus causing a series of serious environmental and social problems. LAAs, such as black carbon and dust, can strongly absorb solar radiation and and have significantly influence on climate change. Moreover, light-absorbing impurities (LAIs) on snow/ice can reduce the snow/ice albedo and further accelerate the snow/ice melting. Both LAAs and LAIs over the TP can induce thermodynamic feedback processes, cause significant warming of the TP and then lead to a strengthening of the early monsoon and affect the subsequent evolution of the monsoon. Many mechanisms have been proposed forth regarding how TP LAAs modulate the phase, intensity, and amplitude of the Asian climate system. A wide range of theoretical, observational, and modeling findings on TP LAAs and their climate impacts are synthesized, in which dust aerosols from drylands and black carbon from biomass burning are considered leading components. By coupling an integrated approach with state-of-the-art modeling, high temporal and fine spatial resolution remote sensing observations with increasing sampling over the TP will provide further insights into TP aerosols. • Light-absorbing aerosols warm the Tibetan Plateau, further influence climate system • The external input of light-absorbing aerosols over the Tibetan Plateau is dominant • Climate effects of light-absorbing aerosols or impurities in snow is divergent [ABSTRACT FROM AUTHOR]

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Water‐soluble organic carbon (WSOC) is a substantial component of carbonaceous aerosols in South/East Asia. However, the poorly constrained sources, molecular compositions, and light absorption properties of WSOC over South/East Asian marine regions lead to large uncertainty in climate effects. Herein, we collected marine aerosol samples from South China Sea to the eastern Indian Ocean to investigate the sources, molecular compositions, and light absorption properties of WSOC. The δ13C of Marine‐influenced WSOC (−20.6 ± 1.4‰) was higher than those in Continent‐influenced (South Asia‐influenced: −24.4 ± 1.1‰ and Southeast Asia‐influenced: −22.7 ± 1.0‰, p < 0.01) regions. Additionally, combining with 5‐day back trajectories and the relationships of δ13C‐WSOC with chemical tracers (Cl−/Na+ and nonsea salt K+/K+), we found that the Marine‐influenced WSOC was mostly related to oceanic emissions, which was more enriched in saturated primary marine biological compounds with lower oxidation level. In contrast, the Continent‐influenced WSOC was significantly affected by C3 biomass burning and secondary organic aerosols formation, and it has a higher fraction of aromatic and highly oxidized compounds. Moreover, the high aromatic level of Continental‐influenced WSOC may result in high mass absorption efficiency at 365 nm (MAE365) but low absorption Ångström exponent (AAE) values. Taken together with previous WSOC light absorption properties studies, we found that the MAE365 of WSOC in urban, rural and background, and marine regions correlated well with AAE. However, the response and correlation coefficients of MAE365 to AAE were highest in urban regions, followed by rural and background and marine regions, which is likely associated with different aromatic compound contents. Therefore, in the future, more attention should be paid to the sources and atmospheric processes of condensed aromatic compounds. Key Points: The Continent‐influenced and Marine‐influenced WSOC were significantly affected by anthropogenic and oceanic emissions, respectivelyThe Continental‐influenced WSOC was more enriched in aromatic compounds, with stronger light absorption capacity than Marine‐influenced WSOCDifference in response and correlation coefficients of MAE365 to AAE in different regions may be related to varied aromatic compound contents [ABSTRACT FROM AUTHOR]

Based on source-specific saccharide tracers, the characteristics of biomass burning (BB) and biogenic emissions of saccharides were investigated in three rural sites at Lincang, which is 65 % covered with forest in the southwest border of China. The total saccharides accounted for 8.4 ± 2.7 % of organic carbon (OC) and 1.6 ± 0.6 % of PM 2.5. The measured anhydrosugars accounted for 48.5 % of total saccharides, among which levoglucosan was the most dominant species. The high level of levoglucosan was both attributed to the local BB activities and biomass combustion smoke transported from the neighboring regions of Southeast Asia (Myanmar) and the northern Indian subcontinent. The measured mono- or disaccharides and sugar alcohols accounted for 24.9 ± 8.3 % and 26.6 ± 9.9 % of the total saccharides, respectively, and both proved to be mostly emitted by direct biogenic volatilization from plant material or surface soils rather than byproducts of polysaccharide breakdown during BB processes. Five sources of saccharides were resolved by non-negative matrix factorization (NMF) analysis, including BB, soil microbiota, plant senescence, airborne pollen, and plant detritus with contributions of 34.0 %, 16.0 %, 21.0 %, 23.7 %, and 5.3 %, respectively. The results provide information on the magnitude of levoglucosan and contributions of BB, as well as the characteristic of biogenic saccharides, at the remote sites of southwest China, which can be further applied to regional source apportionment models and global climate models. [ABSTRACT FROM AUTHOR]