Aerosol chemical components such as black carbon (BC) and brown carbon (BrC) regulate aerosol optical properties, which in turn drive the atmospheric radiative forcing estimations due to aerosols. In this study, we used the long-term measurements from AERONET (Aerosol Robotic Network) to better understand the aerosol types and composition with respect to their seasonal and spatial variabilities in peninsular Southeast Asia (PSEA, here defined as Vietnam, Cambodia, Thailand, Laos, and Myanmar). Two methods (i.e., aerosol type cluster and aerosol component retrieval) were applied to determine the aerosol type and chemical composition during the biomass-burning (BB) season. AERONET sites in northern PSEA showed a higher AOD (aerosol optical depth) compared to that of southern PSEA. Differences in land use pattern, geographic location, and weather regime caused much of the aerosol variability over PSEA. Lower single-scattering albedo (SSA) and higher fine-mode fraction (FMF) values were observed in February and March, suggesting the predominance of BB type aerosols with finer and stronger absorbing particles during the dry season. However, we also found that the peak BB month (i.e., March) in northern PSEA may not coincide with the lowest SSA once dust particles have mixed with the other aerosols. Furthermore, we investigated two severe BB events in March of 2014 and 2015, revealing a significant BrC fraction during BB event days. On high AOD days, although the BC fraction was high, the BrC fraction remained low due to lack of aerosol aging. This study highlights the dominance of carbonaceous aerosols in the PSEA atmosphere during the BB season, while also revealing that transported dust particles and BrC aerosol aging may introduce uncertainties into the aerosol radiative forcing calculation.

Multi year measurements of surface-reaching solar (shortwave) radiation fluxes across a network of aerosol observatories (ARFINET) are combined with concurrent satellite (CERES)-based top of the atmosphere (TOA) fluxes to estimate regional aerosol direct radiative forcing (ARF) over the Indian region. The synergistic approach improves the accuracy of ARF estimates, which otherwise results in an overestimation or underestimation of the atmospheric forcing. During summer, an overestimation of similar to 5 W m(-2) (corresponding heating rate similar to 0.15 K day(-1)) is noticed. The regional average ARF from the synergistic approach reveals the surface forcing reaching -49 W m(-2) over the Indo Gangetic Plains, -45 W m(-2) over northeast India, -34 W m(-2) over the southern Peninsula, and - 16 W m(-2) in the oceanic regions of the Bay of Bengal. The ARF over the northern half of the Indian subcontinent is influenced mainly by anthmpogenic sulfate and carbonaceous aerosols. Dust is dominant in the western region of India during MAM and JJAS. Overall, the clear sky surface reaching solar radiation fluxes is reduced by 3-22% due to the abundance of aerosols in the atmosphere, with the highest reduction over the IGP during autumn and winter.

The properties of the atmospheric aerosols depend on the source region and on the modifications that occur during their transport in the air. We have studied physical and chemical properties of aerosols along with their sink mechanism over two locations in southwest India, an urban site (Pune) and well-established climate observatory at Sinhagad (SINH), which represents rural and high altitude site. The ground-based measurements of aerosols, together with their radiative properties in this study have provided means to understand the observed variability and the impact on the aerosol radiative properties effectively over this region. The annual mean elemental carbon concentration (3.4 mu g m(- 3)) at Pune was observed about three times higher compared to SINH (1.3 mu g m(- 3)), indicating strong emissions of carbon-rich aerosols at the urban location. Aerosol optical properties were derived using the OPAC model which were used to compute the Aerosol radiative forcing (ARF) over both stations calculated using SBDART (Santa Barbara DISORT Atmospheric Radiative Transfer) model shows pronounced seasonal variations due to changes in aerosol optical depth and single scattering albedo at both locations. The year-round ARF was 4-5 times higher over Pune (31.4 +/- 3.5 Wm(- 2)) compared to SINH (7.2 +/- 1.1 Wm(- 2)). The atmospheric heating rate due to aerosols shows a similar pattern as ARF for these locations. The heating was higher in the wintertime, similar to 0.9-1.6 K day(- 1) at Pune, and similar to 0.3-0.6 K day(- 1) at SINH. The estimated scavenging ratio was found high for NO3- and Ca.(2+). The wet deposition fluxes of Cl-, SO42-, Na+, Mg2+ were observed higher for SINH as compared to Pune, due to the high amount of rain received at SINH.

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.