This study reports black carbon (BC) characteristics and climate effects for a 22-month period during 2018-2020 at a receptor location in the eastern Indo-Gangetic Plains (IGP). The overall averaged BC mass concentration was 7.8 & PLUSMN; 4.7 & mu;g m- 3, and the nighttime average (9.1 & PLUSMN; 6.1 & mu;g m- 3) was nearly double that of the daytime (5.8 & PLUSMN; 3.5 & mu;g m- 3). BC was most enhanced during winter, with mean concentration (14.3 & PLUSMN; 3.8 & mu;g m- 3) higher by 4 times as compared to summer. A two-component mixing model, frequency distribution of the Angstrom exponent, and a simultaneous increase in brown carbon (BrC) absorption coefficient suggested that this enhancement was mostly due to the biomass burning (BB) fraction of BC. CALIPSO-derived products showed that the extinction coefficient was highest at 0.62 & PLUSMN; 0.31 km-1 in winter and lowest at 0.12 & PLUSMN; 0.05 km-1 in summer. Backscatter plots and particle depolarization ratios indicated presence of spherical dust particles during summer and smoke plumes during post-monsoon and winter. Concentration-weighted trajectories (CWTs) helped in quantifying significant contributions of the IGP outflow to BC, BC-BB and BrC absorption. Finally, a large direct radiative forcing of the atmosphere by BC (37 & PLUSMN; 22 W m- 2) was estimated via the radiative transfer model SBDART, with an associated atmospheric heating rate of 1.02 K d-1.

The study examines the thermodynamic structure of the marine atmospheric boundary layer (MABL) and its effect on the aerosol dynamics in the Indian Ocean sector of Southern Ocean (ISSO) between 30 degrees S-67 degrees S and 57 degrees E-77 degrees E. It includes observations of aerosols and meteorology collected during the Xth Southern Ocean Expedition conducted in December 2017. The results revealed the effect of frontal-region-specific air-sea coupling on the thermodynamic structure of MABL and its role in regulating aerosols in ISSO. The MABL over the subtropical front was unstable and formed a well-evolved mixed layer ( 2400 m) capped by low-level inversions ( 660 m). Convective activities in the Sub-Antarctic Frontal region were associated with the Agulhas Retroflection Current, which supported the forma-tion of a well-developed mixed layer ( 1860 m). The mean estimates of aerosol optical depth (AOD) and black carbon (BC) mass concentrations were 0.095 +/- 0.006 and 50 +/- 14 ng m-3, respectively, and the resultant clear sky direct shortwave radiative forcing (DARF) and atmospheric heating rate (HR) were 1.32 +/- 0.11 W m-2 and 0.022 +/- 0.002 K day-1, respectively. In the polar front (PF) region, frequent mid-latitude cyclones led to highly stabilized MABL, supported low-level multi-layered clouds (>3-layers) and multiple high-level inversions (strength > 0.5 K m-1 > 3000 m). The clouds were mixed-phased with temperatures less than -12 degrees C at 3000 m altitude. Interestingly, there was higher loading of dust and BC aerosols (276 +/- 24 ng m-3), maximum AOD (0.109 +/- 0.009), clear sky DARF (1.73 +/- 0.02 W m-2), and HR (0.029 +/- 0.005 K day-1). This showed an accumulation of long-range advected anthro-pogenic aerosols within baroclinic-boundaries formed over the PF region. Specifically, in the region south of PF, weak convection caused weakly-unstable MABL with a single low-level inversion followed by no clouds/single-layer clouds. Predominant clean maritime air holding a small fraction of dust and BC accounted for lower estimates of AOD (0.071 +/- 0.004), BC concentrations (90 +/- 55 ng m-3) and associated clear sky DARF and HR were 1.16 +/- 0.06 W m-2 and 0.019 +/- 0.001 K day-1, respectively.

The optical and radiative characteristics of water-soluble and carbonaceous aerosol species in the PM2.5 samples were examined for a representative megacity over the Indo-Gangetic Basin (IGB). Aerosol optical and radiative transfer models were used to extract sulphate (SO4), nitrate (NO3), organic carbon (OC) and elemental carbon (EC) from the observations done in 2012. Initial results suggest that the mass concentration of OC dominated over other species, but impacts on optical characteristics were mostly due to the SO4 aerosols. Further, EC shows relatively large impact on radiative forcing. The aerosol optical depth (AOD) at 500 nm for SO4, NO3, EC and OC was found to be contributing similar to 36%, 20%, 27% and 9%, respectively in the total AOD value (0.61 +/- 0.18) during the entire study period. The single scattering albedo (SSA) for SO4 and NO3 was high and suggested their scattering nature; however, being the highly absorbing species, EC was found to show the lowest values of SSA during the study period. SSA for OC was, however, similar to 0.70, which was found to show the second highest warming species in the atmosphere with contribution of similar to 10%, after EC, which caused the highest warming (similar to 70%), to the total atmospheric forcing.

This study reports comprehensive analysis of seasonal and inter-annual variations of aerosol properties (optical, physical and chemical) and radiative effects over Pokhara Valley in the foothills of central Himalayas in Nepal utilizing the high-quality multi-year columnar aerosol data observed recently from January 2010 to December 2017. This paper focusses on the seasonal and inter-annual variations of chemical (composition), and absorption properties of aerosols and their radiative effects. The single scattering albedo (SSA) either decreases as a function of wavelength or remains independent of wavelength. The seasonal mean aerosol absorption optical depth (AAOD) exhibits a behavior opposite to that of SSA. Carbonaceous aerosols (CA) dominate (>= 60%) aerosol absorption during the whole year. Black carbon (BC) alone contributes >60% to AAOD(C)(A) while brown carbon (BrC) shares the rest. The absorbing aerosol types are determined to be BC, and mixed (BC and dust) only. Dust as absorbing aerosol type is absent over the Himalayan foothills. The ARF(SFC) is >= -50 Wm(-2) except in monsoon almost every year. The ARF(ATM) is >= 50 Wm(-2) during winter and pre-monsoon in all the years. ARFE(SFC), ARFE(TOA) and ARFE(ATM) follow a similar pattern as that of ARF. High values of ARFE at SFC, TOA and ATM (except during monsoon when values are slightly lower) suggest that aerosols are efficient in significantly modulating the incoming solar flux throughout the year. The annual average aerosol-induced atmospheric heating rate (HR) over Pokhara is nearly 1 K day(-1) every year during 8-year observation, and is highest in 2015 (similar to 2.5 K day(-1)). The HR is about 1 K day(-1) or more over all the locations in IGP during the year. These quantitative results can be used as inputs in global/regional climate models to assess the climate impact of aerosols, including on regional temperature, hydrological cycle and melting of glaciers and snowflelds in the region. (C) 2020 Elsevier Ltd. All rights reserved.

The simultaneous near surface measurements of aerosol scattering and absorption coefficients over different environments (Ahmedabad, urban and Gurushikhar, a high altitude remote site) in western India were conducted to estimate SSA and investigate the importance of SSA in aerosol radiative forcing. The surface SSA (0.79, 0.85) is lower than the column SSA (0.92, 0.95) as emission sources for black carbon aerosols (absorbing in nature) are abundant near the surface (Ahmedabad, Gurushikhar). The atmospheric warming over the urban region estimated using column SSA is a factor of 3 lower ( similar to 18 Wm(-2)) than that of the warming ( similar to 52 Wm(-2)) estimated utilising surface SSA. The significant difference in atmospheric warming arises due to the differences in the SSA as aerosol optical depth (a measure of column concentration of aerosols) is the same. Surface and column SSA are comparatively higher over the high altitude remote site as the abundance of absorbing aerosols is less over a non-source region. In addition, the differences between surface and column SSA are less (< 9%) resulting in comparable aerosol radiative forcing estimates. This study highlights the differences that can arise in aerosol radiative effects due to the differences in SSA as a function of altitude (surface vs. column) and environment (urban vs. remote), thereby providing regional bounds on aerosol radiative forcing which can further be used in climate assessment studies.

A modeling framework was used to examine gaps in understanding of seasonal and spatial heterogeneity in aerosol abundance and radiative forcing over northern South Asia, whose glimpses are revealed in observational studies. Regionally representative emissions were used in chemical transport model simulations at a spatial resolution of 60 x 60 km(2), in April, July and September, chosen as months of contrasting emissions and rainfall. Modeled aerosol abundance in northern South Asia was predominantly found to be dust and carbonaceous in April, dust and sulfate in July and sulfate and carbonaceous in September. Anthropogenic aerosols arose from energy-use emissions (from industrial sources, residential biofuel cooking, brick kilns) in all months, additionally from field burning in April, and incursion from East Asia in September. In April, carbonaceous aerosols were abundant from open burning of agricultural fields even at high altitude locations (Godavari), and of forests in the eastern Gangetic Plain (Kolkata). Direct radiative forcing and heating rate, calculated from OPAC-SBDART, using modeled aerosol fields, and corrected by MODIS AOD observations, showed regionally uniform atmospheric forcing in April, compared to that in other months, influenced by both dust and black carbon abundance. A strong spatial heterogeneity of radiative forcing and heating rate was found, with factor of 2.5-3.5 lower atmospheric forcing over the Tibet plateau than that over the Ganga Plain and Northwest in July and September. However, even over the remote Tibet plateau, there was significant anthropogenic contribution to atmospheric forcing and heating rate (45% in Apr, 75% in Sep). Wind fields showed black carbon transport from south Asia in April and east Asia in September. Further evaluation of the transport of dust and anthropogenic emissions from various source regions and their deposition in the Himalaya and Tibet, is important in understanding regional air quality and climate change over this ecosystem. (C) 2015 Elsevier Ltd. All rights reserved.

Observations on black carbon (BC) aerosols over an urban site (Pune) and a rural, high altitude site (Sinhagad) during summer and winter seasons over the period of 2009-2013 are reported. Apart from the temporal variation of BC over both the sites, its mass fraction to total suspended particulates (TSP) is studied. Finally, using the chemical composition of TSP and BC in the OPAC model, season-wise optical properties of aerosols are obtained which are further used in the SBDART model to derive the aerosol radiative forcing (ARF) at surface and top of the atmosphere and thereby the atmospheric forcing and heating rates in each season over both the sites. BC mass concentration and its mass fraction to TSP (Mf BC) were higher at Pune than at Sinhagad, indicating impact of more anthropogenic sources. At both the sites winter season witnessed higher BC concentrations than summer as well as higher Mf BC which is due to the prevailing favorable meteorological conditions in winter. Diurnal variation of BC showed different patterns at Pune and Sinhagad in terms of strength and occurrence of high and low values that could be attributed to varying local boundary layer conditions and source activities at both the sites. Negative ARF indicated cooling at top of the atmosphere and at surface leading to warming of the atmosphere at both the sites. However, surface cooling and atmospheric warming was more dominant at Pune leading to higher atmospheric heating rates, underlining the impact of absorbing BC aerosols which were about three times more at Pune than Sinhagad. (C) 2015 Elsevier Ltd. All rights reserved.

The higher altitude regions of Himalayas and Tibetan Plateau are influenced by the dust and black carbon (BC) aerosols from the emissions and long-range transport from the adjoining areas. In this study, we present impacts of advection of polluted air masses of natural and anthropogenic emissions, on aerosol optical and radiative properties at Manora Peak (similar to 2000 m amsl) in central Himalaya over a period of more than two years (February 2006-May 2008). We used the most updated and comprehensive data of chemical and optical properties available in one of the most climatically sensitive region, the Himalaya, to estimate atmospheric radiative forcing and heating rate. Aerosol optical depth (ADD) was found to vary from 0.04 to 0.45 with significantly higher values in summer mainly due to an increase in mineral dust and biomass burning aerosols due to transport. In contrast, single scattering albedo (SSA) varied from 0.74 to 0.88 with relatively lower values during summer, suggesting an increase in absorbing BC and mineral dust aerosols. As a result, a large positive atmospheric radiative forcing (about 28 5 Wm(-2)) and high values of corresponding heating rate (0.80 +/- 0.14 Kday(-1)) has been found during summer. During the entire observation period, radiative forcing at the top of the atmosphere varied from 2 to +14 Wm(-2) and from -3 to -50 Wm(-2) at the surface whereas atmospheric forcing was in the range of 3 to 65 Wm(-2) resulting in a heating rate of 0.1-1.8 Kday(-1). (C) 2014 Elsevier B.V. All rights reserved.

The present work is aimed to understand direct radiation effects due to aerosols over Delhi in the Indo-Gangetic Basin (IGB) region, using detailed chemical analysis of surface measured aerosols during the year 2007. An optically equivalent aerosol model was formulated on the basis of measured aerosol chemical compositions along with the ambient meteorological parameters to derive radiatively important aerosol optical parameters. The derived aerosol parameters were then used to estimate the aerosol direct radiative forcing at the top of the atmosphere, surface, and in the atmosphere. The anthropogenic components measured at Delhi were found to be contributing similar to 72% to the composite aerosol optical depth (AOD(0.5) similar to 0.84). The estimated mean surface and atmospheric forcing for composite aerosols over Delhi were found to be about -69, -85, and -78 W m(-2) and about +78, +98, and +79 W m(-2) during the winter, summer, and post-monsoon periods, respectively. The anthropogenic aerosols contribute similar to 90%, 53%, and 84% to the total aerosol surface forcing and similar to 93%, 54%, and 88% to the total aerosol atmospheric forcing during the above respective periods. The mean (+/- SD) surface and atmospheric forcing for composite aerosols was about -79 (+/- 15) and +87 (+/- 26) W m(-2) over Delhi with respective anthropogenic contributions of similar to 71% and 75% during the overall period of observation. Aerosol induced large surface cooling, which was relatively higher during summer as compared to the winter suggesting an increase in dust loading over the station. The total atmospheric heating rate at Delhi averaged during the observation was found to be 2.42 +/- 0.72 K day(-1), of which the anthropogenic fraction contributed as much as similar to 73%.

The effects of black carbon (BC) aerosol radiative forcing on spring rainfall in Southeast Asia are studied using numerical simulations with the NASA finite-volume General Circulation Model (fvGCM) forced with monthly varying three-dimensional aerosol distributions from the Goddard Ozone Chemistry Aerosol Radiation and Transport model (GOCART). During the boreal spring, March-April-May (MAM), BC from local emissions accumulates over Southeast Asia. The BC aerosol layer, which extends from the surface to higher elevation above planetary boundary layer (PBL), absorbs solar radiation and heats the mid-troposphere through a semi-direct effect over regions of large aerosol optical thickness (AOT) and thereby significantly perturbs large-scale and meridional circulations. Results show that anomalous precipitation patterns and associated large-scale circulations induced by radiative forcing by BC aerosol can explain observed precipitation reductions, especially over Southeast Asia. Therefore, BC aerosol forcing may be one of the important factors affecting the spring rainfall trend over Southeast Asia. (C) 2010 Elsevier Ltd. All rights reserved.