Analysis of South Asian Monsoons within the Context of Increasing Regional Black Carbon Aerosols

South Asian monsoons were analyzed within the context of increasing emissions of black carbon(BC) aerosols using a global atmospheric general circulation model.The BC aerosols were allowed to increase only over the south Asian domain to analyze the impacts of regional black carbon over the climatological patterns of monsoons.The black carbon significantly absorbed the incoming short wave radiation in the atmosphere,a result that is consistent with previous studies.Pre-monsoon(March-April-May) rainfall showed positive anomalies,particularly for some coastal regions of India.The summer(June-July-August) rainfall anomalies were negative over the northern Himalayas,Myanmar,southern China,and most of the regions below 20°N due to the decrease in temperature gradients induced by the absorption of radiation by BC aerosols.The vertical wind speed anomalies indicated that these regions experienced less convection,which reduces the precipitation efficiency of the monsoon system in South Asia.     

Atmospheric Aerosol Characterization Over Naples During 2000–2003 EARLINET Project: Planetary Boundary-Layer Evolution and Layering

The evolution of the planetary boundary layer and the influence of local circulation phenomena over Naples (southern Italy, 40.838° N, 14.183° E, 118 m above sea level) have been studied by systematic lidar measurements of aerosol optical properties and vertical distributions carried out from May 2000 to August 2003, in the course of the EARLINET project. In particular, our data show the development of aerosol layers typically located in the range between 1,000 and 2,300 m, with variable thickness. The optical properties of the observed layers have been determined. In order to analyse the evolution of the planetary boundary layer, detailed observations of complete diurnal cycles have also been performed. The analysis of lidar measurements of vertical profiles of wind speed and wind direction and air mass back-trajectories allowed us to characterize the sea-breeze circulation influence on both the planetary boundary-layer evolution and the observed aerosol vertical distribution.     

中国区域气溶胶对东亚夏季风的可能影响（I）：硫酸盐气溶胶的影响

 利用NCAR的新一代GCM CAM3.0模式离线耦合一个气溶胶同化系统,模拟研究了中国区域硫酸盐气溶胶的直接气候效应对东亚夏季风及其降水的影响。结果显示：中国区域硫酸盐气溶胶引起全球平均的直接辐射强迫为-0.25 W/m²,中国内陆约25°N以北普遍降温,而海表温度升高。由此导致海陆温差缩小,东亚夏季风强度减弱,中国地区季风降水明显减少,而尤以积云降水减少起主要作用。硫酸盐气溶胶对中国地区的对流活动起抑制作用。     

Particulate PAHs levels at Mt. Halla site in Jeju Island, Korea: Regional background levels in northeast Asia

The levels of PM.25 PAHs at Mt. Halla site, Jeju Island, a background site in Korea were observed between March 1999 and March 2002. A seasonal variation was observed for the particulate PAHs concentrations with high levels during cold season similar to Gosan, a nearby coastal background site, due to the seasonal variations of fossil fuel usage in Asia. The total average concentration of ambient particulate PAHs was 404 ± 579 pg m^− 3, about one order lower than the ambient level at Gosan. However, the ratios of the anthropogenic inorganic ion concentrations between Mt. Halla and Gosan were smaller, 1.5 for non sea-salt (nss) sulfate and 2.7 for nitrate. Two possible explanations for these characteristics are (1) two sites measured different air parcels and/or (2) the effect of local emissions were different at two sites. Based on the Bep/BaP ratio result, upper air wind direction data, backward trajectory analysis, and LIDAR measurement data at Gosan, it was found that the degree of the effects of local emissions to the sampling sites be the major reason for the different PAHs levels at two sites though, in some cases, the air parcels arriving at Mt. Halla were different from those arriving at Gosan. For secondary aerosol such as nss sulfate, the lower concentration difference indicates both site are affected by regional transport. It points that the measurement result for directly emitted species such as PAHs at Gosan might be significantly influenced by local emissions.     

香港气溶胶烃类物质组成,分布及来源初探

总悬浮颗粒和１０μｍ以下人体可吸入颗粒物，即ＲＳＰ样品采自香港市区和郊区，样品采用超声抽提和硅胶层析柱分离，使用气相色谱，气相色谱－质谱（ＧＣ，ＧＣ－ＭＳＤ）分析饱和烃和芳烃馏分。研究表明，ＴＳＰ样品中含有化石燃料燃烧和生物来源的脂肪烃，包括正构烷烃，甾烷和藿烷类等有机物。芳香烃主要由２－７环的多环芳烃组成，其中１０种属美国优先控制污染物，ＲＳＰ样品中主要含生物来源的正构烷烃，含少量代表化石燃烧产     

Effect of synoptic meteorological conditions on aerosol properties over urban environment: A study over tropical urban region of Hyderabad,India

Aerosol particle size distribution and chemical properties are important in studies related to human health and climate. The present study describes an analysis of aerosol mass loading, Aerosol Optical Depth (AOD), black carbon aerosol mass concentration and carbon monoxide over tropical urban region of Hyderabad, India, during March 2006, coinciding with active forest fires season over India. Aerosol optical depth, particulate matter mass loading and carbon monoxide were observed to be high on days with air mass coming from north of the study area. Spatial occurrence of forest fires was analysed using MODIS daytime data and DMSP-OLS nighttime data sets. Aerosol optical depth measured using Microtops-II sunphotometer correlated well with MODIS derived AOD values. Results of the study suggested that synoptic meteorological conditions play an important role in the observed aerosol properties over the study area during the forest fire season.     

Laser desorption/ionization mass spectrometric study of secondary organic aerosol formed from the photooxidation of aromatics

Five aromatic hydrocarbons – benzene, toluene, ethylbenzene, p-xylene and 1,2,4-trimethylbenzene – were selected to investigate the laser desorption/ionization mass spectra of secondary organic aerosols (SOA) resulting from OH-initiated photooxidation of aromatic compounds. The experiments were conducted by irradiating aromatic hydrocarbon/CH₃ONO/NO _X mixtures in a home-made smog chamber. The aerosol time-of-flight mass spectrometer (ATOFMS) was used to measure the aerodynamic size and chemical composition of individual secondary organic aerosol particles in real-time. Experimental results showed that aerosol created by aromatics photooxidation is predominantly in the form of fine particles, which have diameters less than 2.5 μm (i.e. PM2.5), and different aromatic hydrocarbons SOA mass spectra have eight same positive laser desorption/ionization mass spectra peaks: m/z = 18, 29, 43, 44, 46, 57, 67, 77. These mass spectra peaks may come from the fragment ions of the SOA products: oxo-carboxylic acids, aldehydes and ketones, nitrogenated organic compounds, furanoid and aromatic compounds. The possible reaction mechanisms leading to these products were also discussed.     

中国大陆火山活动对气候与环境影响的研究进展

本文简要回顾了我国中、新生代典型中酸性火山活动的气候环境效应的研究进展,重点讨论了新生代长白山天池火山喷发和中生代辽西火山活动对气候环境造成的影响。天池火山气体含量呈现两个相同趋势的旋回式变化,从早到晚,卤化物和H2O呈降低趋势,而硫化物气体呈增加趋势。火山旋回早期富含HF气体导致动物窒息、甚至大批集群死亡;晚期喷出的大量硫化物气体可以形成大规模酸雨和剧毒火山灰云幕,对周围的动植物生长有严重影响。辽西火山气体可分为三种组合,形成酸雨,导致地表温度下降,加速臭氧浓度降低,甚至破坏臭氧层,从而对生物的生存环境造成严重危害。     

Traffic aerosols (18 nm particle size 18 μm) source apportionment during the winter period

In November 2004–January 2005, a micro orifice uniform deposit impactor (MOUDI) and a Nanometer (nanometer)-MOUDI were used in the center of Taiwan to measure particle size (18 nm particle size 18 μm) distributions of atmospheric aerosols at a traffic site during the winter period. The average Mass in Media Aerodynamic Diameter (MMAD) of suspended particles is 0.99 μm this study. As for the ultra fine and nanometer (nanometer) particle mode, the composition order for these major ions species was SO₄²⁻ NH₄⁺ NO₃⁻ Mg²⁺ Ca²⁺ Na⁺ K⁺ Cl⁻. An ion Chromatography (DIONEX-100) was used to analyze major anion species, Cl⁻, NO₃⁻, SO₄²⁻ and cation species, NH₄⁺Na⁺, K⁺, Ca²⁺Mg²⁺. Their concentrations were also extracted from various particles size modes (nanometer (nanometer), ultra fine, fine and coarse). The results obtained in this study also indicated that the average portions for the major ionic species (SO₄²⁻, NH₄⁺ and Mg²⁺) in the nanometer (nanometer), ultra fine, fine and coarse particulate modes are about 34%, 37%, 63% and 30%, respectively at this traffic sampling site during the winter period.     

Aerosol Chemistry, and Light-Scattering and Hygroscopicity Budgets during Outflow from East Asia

During the ACE-Asia field campaign, 41 aerosol filter samples were obtained by airborne sampling over the ocean to the north, south and west of Japan, generally under conditions of outflow from the Asian continent. These samples were analyzed for their water-soluble chemical components, particularly organic species. Suites of inorganic anions, carbohydrates, organic acids and metallic elements were identified and quantified (21 distinct species). Simultaneously, measurements were made of the aerosol hygroscopicity and light scattering. A factor analysis performed on the compositional data identified several sources for the aerosols sampled during the field campaign. Regression of the light-scattering data onto tracers for each of these factors suggests that the aerosol light scattering could be largely attributed to three of these factors: anthropogenic emissions, biomass burning, and soil dust. Similarly, the aerosol hygroscopicity was largely consistent with an empirical mixing model based on past measurements of the hygroscopicity of these individual aerosol types. Limited size-resolved , aerosol composition measurements were also obtained and suggested different sources for various chemical species.