Spatial and temporal variations of aerosols around Beijing in summer 2006: Model evaluation and source apportionment

Regional aerosol model calculations were made using the Weather Research and Forecasting (WRF)-Community Multiscale Air Quality (CMAQ) and WRF-chem models to study spatial and temporal variations of aerosols around Beijing, China, in the summer of 2006, when the Campaigns of Air Quality Research in Beijing and Surrounding Region 2006 (CAREBeijing) intensive campaign was conducted. Model calculations captured temporal variations of primary (such as elemental carbon. (EC)) and secondary (such as sulfate) aerosols observed in and around Beijing. The spatial distributions of aerosol optical depth observed by the MODTS satellite sensors were also reproduced over northeast China. Model calculations showed distinct differences in spatial distributions between primary and secondary aerosols in association with synoptic-scale meteorology. Secondary aerosols increased in air around Beijing on a scale of about 1000 × 1000 km2 under an anticyclonic pressure system. This air mass was transported northward from the high anthropogenic emission area extending south of Beijing with continuous photochemical production. Subsequent cold front passage brought clean air from the north, and polluted air around Beijing was swept to the south of Beijing. This cycle was repeated about once a week and was found to be responsible for observed enhancements/reductions of aerosols at the intensive measurement sites. In contrast to secondary aerosols, the spatial distributions of primary aerosols (EC) reflected those of emissions, resulting in only slight variability despite the changes in synopticscale meteorology. In accordance with these results, source apportionment simulations revealed that primary aerosols around Beijing were controlled by emissions within 100 km around Beijing within the preceding 24 h, while emissions as far as 500 km and within the preceding 3 days were found to affect secondary aerosols. Copyright 2009 by the American Geophysical Union

Characterization of Electronic Cigarette Aerosol and Its Induction of Oxidative Stress Response in Oral Keratinocytes.

In this study, we have generated and characterized Electronic Cigarette (EC) aerosols using a combination of advanced technologies. In the gas phase, the particle number concentration (PNC) of EC aerosols was found to be positively correlated with puff duration whereas the PNC and size distribution may vary with different flavors and nicotine strength. In the liquid phase (water or cell culture media), the size of EC nanoparticles appeared to be significantly larger than those in the gas phase, which might be due to aggregation of nanoparticles in the liquid phase. By using in vitro high-throughput cytotoxicity assays, we have demonstrated that EC aerosols significantly decrease intracellular levels of glutathione in NHOKs in a dose-dependent fashion resulting in cytotoxicity. These findings suggest that EC aerosols cause cytotoxicity to oral epithelial cells in vitro, and the underlying molecular mechanisms may be or at least partially due to oxidative stress induced by toxic substances (e.g., nanoparticles and chemicals) present in EC aerosols

Radiative absorption enhancement of dust mixed with anthropogenic pollution over East Asia

The particle mixing state plays a significant yet poorly quantified role in aerosol radiative forcing, especially for the mixing of dust (mineral absorbing) and anthropogenic pollution (black carbon absorbing) over East Asia. We have investigated the absorption enhancement of mixed-type aerosols over East Asia by using the Aerosol Robotic Network observations and radiative transfer model calculations. The mixed-type aerosols exhibit significantly enhanced absorbing ability than the corresponding unmixed dust and anthropogenic aerosols, as revealed in the spectral behavior of absorbing aerosol optical depth, single scattering albedo, and imaginary refractive index. The aerosol radiative efficiencies for the dust, mixed-type, and anthropogenic aerosols are −101.0, −112.9, and −98.3 Wm⁻²τ⁻¹ at the bottom of the atmosphere (BOA); −42.3, −22.5, and −39.8 Wm⁻²τ⁻¹ at the top of the atmosphere (TOA); and 58.7, 90.3, and 58.5 Wm⁻²τ⁻¹ in the atmosphere (ATM), respectively. The BOA cooling and ATM heating efficiencies of the mixed-type aerosols are significantly higher than those of the unmixed aerosol types over the East Asia region, resulting in atmospheric stabilization. In addition, the mixed-type aerosols correspond to a lower TOA cooling efficiency, indicating that the cooling effect by the corresponding individual aerosol components is partially counteracted. We conclude that the interaction between dust and anthropogenic pollution not only represents a viable aerosol formation pathway but also results in unfavorable dispersion conditions, both exacerbating the regional air pollution in East Asia. Our results highlight the necessity to accurately account for the mixing state of aerosols in atmospheric models over East Asia in order to better understand the formation mechanism for regional air pollution and to assess its impacts on human health, weather, and climate

Polarized light scattering by aerosols in the marine atmospheric boundary layer

The intensity and polarization of light scattered from marine aerosols affect visibility and contrast in the marine atmospheric boundary layer (MABL). The polarization properties of scattered light in the MABL vary with size, refractive index, number distributions, and environmental conditions. Laboratory measurements were used to determine the characteristics and variability of the polarization of light scattered by aerosols similar to those in the MABL. Scattering from laboratory-generated sea-salt-containing (SSC) [NaCl, (NH4)2SO4, and seawater] components of marine aerosols was measured with a scanning polarization-modulated nephelometer. Mie theory with Gaussian and log normal size distributions of spheres was used to calculate the polarized light scattering from various aerosol composition models and from experimentally determined distributions of aerosols in the marine boundary layer. The modeling was verified by comparison with scattering from distilled water aerosols. The study suggests that polarimetric techniques can be used to enhance techniques for improving visibility and remote imaging for various aerosol types, Sun angles, and viewing conditions

Turbulent thermal diffusion of aerosols in geophysics and laboratory experiments

We discuss a new phenomenon of turbulent thermal diffusion associated with turbulent transport of aerosols in the atmosphere and in laboratory experiments. The essence of this phenomenon is the appearance of a nondiffusive mean flux of particles in the direction of the mean heat flux, which results in the formation of large-scale inhomogeneities in the spatial distribution of aerosols that accumulate in regions of minimum mean temperature of the surrounding fluid. This effect of turbulent thermal diffusion was detected experimentally. In experiments turbulence was generated by two oscillating grids in two directions of the imposed vertical mean temperature gradient. We used Particle Image Velocimetry to determine the turbulent velocity field, and an Image Processing Technique based on an analysis of the intensity of Mie scattering to determine the spatial distribution of aerosols. Analysis of the intensity of laser light Mie scattering by aerosols showed that aerosols accumulate in the vicinity of the minimum mean temperature due to the effect of turbulent thermal diffusion. Geophysical applications of the obtained results are discussed.Comment: 9 pages, 6 figures, revtex

Aerosols Protocol

The purpose of this activity is to measure the aerosol optical thickness of the atmosphere (how much of the sun's light is scattered or absorbed by particles suspended in the air). Students point a GLOBE sun photometer at the sun and record the largest voltage reading they obtain on a digital voltmeter connected to the photometer. Students observe sky conditions near the sun, perform the Cloud, Optional Barometric Pressure (optional) and Relative Humidity Protocols, and measure current air temperature. Intended outcomes are that students will understand the concept that the atmosphere prevents all of the sun's light from reaching Earth's surface and they learn what causes hazy skies. Supporting background materials for both student and teacher are included. Educational levels: Middle school, High school

Aerosols Loading Trends and its Environmental Threats Over Cotonou-Benin.

Environmental security is totally relegated in countries of West Africa. The monitoring of the aerosols loading over Cotonou was the aim of this study. The outcome of our finding has salient links to food security, aviation and communication industry, thermal comfort and climate system of Benin. Cotonou is located on longitude 2.43°E and latitude 6.37°N. Fifteen years data were obtained from the multiangled spectro-reflectometry (MISR). The aerosol loading was monitored using analytical and statistical techniques. The aerosols retention over Cotonou was high in 2000 (69.91%), 2008 (72%) and 2013 (42.45%). This means that there is the possibility of higher rising sea levels and exposure to coastal erosion due to a twisted cloud formation

Constraints on climate forcing by sulphate aerosols from seasonal changes in Earth's spin

Angular momentum exchanges between atmosphere and solid Earth are strongly modulated by variations in global atmospheric circulation. Geodetically determined length-of-day (LOD) fluctuations provide an independent resource to investigate climate changes. Here, I evaluate the effects of volcanic and anthropogenic sulphate aerosols on Earth’s rotational energy variations. The period analysed, 1980–2002, shows that the strongest seasonal LOD variations are related to sulphate peak concentrations from the El-Chichon 1982, and Pinatubo and Cerro ´ Hudson 1991 volcanic eruptions. The Earth’s rotational energy budget implies that radiative forcing alone cannot produce the observed LOD anomalies. Rather, the required amount of atmospheric kinetic energy can be explained only by a strong influence of sulphate aerosols on energy partitioning into the atmosphere, for example, as sulphate aerosols affect latent heat release and transport during condensation–evaporation–freezing cycles. Overall, the effects of sulphate aerosols on Earth’s spin changes are faster than those produced by greenhouse gases