The monthly/seasonal characteristics of the concentration and aerosol optical depth (AOD) of four aerosol components (water-soluble, insoluble, black carbon (BC), and sea-salt) and their direct radiative forcing (DRF) were investigated at three environmental locations in Southeast Texas. We used fine particulate matter (PM2.5) samples measured at one urban residential (Aldine (AD)) and two suburban (Deer Park (DP) and West Liberty (WL)) sites located around Houston during 2016-2017, and performed model-based analysis using the mass concentrations of the four aerosol components to evaluate their impact on the DRF. Overall, the concentrations, AODs, and DRFs of all four aerosol components at AD were higher than those at DP and WL during the study period. In particular, the water-soluble component was the most dominant contributor, except for absorbing BC. The monthly AOD patterns of the four individual aerosol components (especially, water-soluble and BC) at the three sites were found to have strong associations with their concentrations and/or relative humidity (RH). The DRFs at the top of the atmosphere (DRFTOA) and surface level (DRFSFC) for most of the aerosol components were found to be highest in winter 2017 (AD), spring 2016 and winter 2017 (DP), and winter 2016 and fall 2017 (WL). The exceptions were sea-salt and insoluble components, which showed a peak in summer 2016 and no distinct monthly variation, respectively. Uncertainties in the DRFs of the four target aerosol components calculated using in-situ RH measurements were found to be less than 20%, with the exception of the water-soluble component at WL (24%). A sensitivity test showed that the DRFs of the aerosol components were slightly and significantly influenced by changes in AOD and single scattering albedo, respectively; additionally, sensitively changed with RH.

The properties of summer radiation and aerosols were studied at Xinzhou, a suburban site on the North China Plain (NCP) by using ground-based measurements in 2014. The radiation detections under clear and cloudy skies showed that longwave radiation presented a sigmate pattern, with a maximum of 392.6 W m(-2) at 1700 local standard time (LST) associated with the cloud radiative forcing, and a minimum of 360.0 W m(-2) at 0600 LST when the lowest surface temperature (17.1 degrees C) occurred. Solar radiation, including global, direct, diffuse, photosynthetically active, ultraviolet-A, and ultraviolet-B, exhibited a single peak at similar to 1300 LST. A bimodal size distribution, with fine mode aerosols showing a peak between 0.1 and 0.2 mu m and coarse mode aerosols showing a peak at similar to 5 mu m, was observed at Xinzhou. The dominant aerosol type was black carbon coating on coarse particles (85.7%) for the cases with aerosol optical depth at 400 nm (AOD) greater than 0.4, leading to a lower single scattering albedo (0.81) than the typical value (similar to 0.90) at the other stations on the NCP. The mean values of EAE and AAE (extinction and absorption angstrom ngstrom exponent, respectively) were 1.14 +/- 0.15 and 0.58 +/- 0.28 for the aerosol measurements. The average of instantaneous aerosol direct radiative forcing at the bottom of the atmosphere was -138.9 +/- 33.0 W m(-2)for the cases with AOD > 0.4. The results in this study are expected to improve understanding at suburban sites on the NCP of aerosol properties and their impacts on regional radiation budgets.

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.

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.