Aerosol radiative properties using recently available high-quality columnar aerosol data collected at several AERONET sites in South Asia, with a focus on pollution outflow from continental South Asia observed over Hanimaadhoo in Maldives, a small island in northern Indian Ocean are quantified. The seasonal mean aerosol optical depth (AOD) over Hanimaadhoo is >= 0.3 (except ca. 0.2 during monsoon season), and single scattering albedo (SSA) is > 0.90 in all seasons. Fine mode aerosols contribute dominantly to AOD. SSA decreases as a function of wavelength due to influence of continental aerosols, except during the monsoon season when its spectral trend reverses due to increase in dust. Carbonaceous aerosols dominate (>90%) contribution to absorption AOD (AAOD). Black carbon (BC) and brown carbon (BrC) contribute >75% and -25 Wm(-2), > -20 Wm(-2) and similar to+20 Wm(-2), respectively. Aerosol loading and atmospheric heating have increased over this background site over the last decade. A regional-scale analysis of aerosol properties and radiative effects across and surrounding the Indo-Gangetic Plain (IGP) shows that AOD is >= 0.3 over entire region, and aerosols reduce seasonally 30-50 Wm(-2) of solar radiation reaching the surface, contributing significantly to solar dimming effect. The atmospheric solar heating rate due to aerosols (HR) is >= 1 K day(-1) across IGP. These high ARFs, ARFE(SFC) and HR, and increasing trends have significant implications to climate and hydrological cycle over South Asia and beyond.
Pollutants, which are usually transported from urban cities to remote glacier basins, and aerosol impurities affect the earth's temperature and climate by altering the radiative properties of the atmosphere. This work focused on the physicochemical properties of atmospheric pollutants across the urban and remote background sites in northwest China. Information on individual particles was obtained using transmission electron microscopy (TEM) and energy dispersive X-ray spectrometry (EDX). Particle size and age-dependent mixing structures of individual particles in clean and polluted air were investigated. Aerosols were classified into eight components: mineral dust, black carbon (soot)/fly ash, sulfates, nitrates, NaCI salt, ammonium, organic matter, and metals. Marked spatial and seasonal changes in individual particle components were observed in the study area. Aerosol particles were generally found to be in the mixing state. For example, salt-coated particles in summer accounted for 31.2-44.8% of the total particles in urban sites and 37.5-74.5% of the total particles in background sites, while in winter, almost all urban sites comprised >50%, which implies a significant effect on the radiative forcing in the study area. We found that in PM2.5 section, the internally mixed black carbon/organic matter particles clearly increased with diameter. Moreover, urban cities were characterized by atmospheric particles sourced from anthropogenic activities, whereas background locations exhibited much lower aerosol concentrations and increased particle density, originating from natural crustal sources (e.g., mineral dust and NaCI salt), which, together with air mass trajectory analysis, indicates a potential spatial transport process and routes of atmospheric transport from urban cities to background locations. Thus, this work is of importance in evaluating atmospheric conditions in northwest China and northeast Tibetan Plateau regions, to discover the transport processes and facilitate improvements in climatic patterns concerning atmospheric impurities. (C) 2018 Elsevier Ltd. All rights reserved.