气溶胶元素碳的测量及其与虚折射率的相关性

大气气溶胶的虚折射率是大气气溶胶的一个重要物理参数,它表示气溶胶对光辐射的吸收特性。大气气溶胶中的元素碳是重要的吸光物质。因此,对大气气溶胶中元素碳的测量及与大气气溶胶虚折射率测量的相关性研究具有重要意义。 本文提供了利用240C元素分析仪测量大气气溶胶中元素碳含量的方法,并对大气气溶胶元素碳含量与大气气溶胶虚折射率的测量结果作了相关性分析。结果表明,两者之间存在明显的正相关。     

Source attribution of urban smog episodes caused by coal combustion

Stable weather conditions together with extensive use of coal combustion often lead to severe smog episodes in certain urban environments, especially in Eastern Europe. In order to identify the specific sources that cause the smog episodes in such environments, and to better understand the mixing state and atmospheric processing of aerosols, both single particle and bulk chemical characterization analysis of aerosols were performed in Krakow, Poland, during winter 2005.Real-time measurements of the bulk PM10 aerosol during a severe smog episode (PM10 mass > 400 µg m^− 3) showed a stable concentration of black carbon in the aerosol, and an increase in the sulphate and chlorine mass contributions towards the end of the episode. Chemical characterization of single particles further helped to identify residential coal burning as the main source that caused this severe smog episode, consisting of single particles with major signals for carbon with simultaneous absence of sulphate, chlorine and calcium. Particles from industrial coal combustion gained importance towards the end of that episode, after residential coal combustion was switched off, indicated by an increase of the percentage of sulphate and chlorine containing particles. Traffic was not a significant source during the severe smog episode. During a lighter smog episode, residential and industrial coal combustion was still predominant, with an increased contribution of traffic and processed/aged aerosols. On a clean day, particle classes containing nitrate were the most abundant. In addition, the aerosol was more internally mixed showing that there were more sources contributing to the total aerosol population.     

Correlation between black carbon aerosols, carbon monoxide and tropospheric ozone over a tropical urban site

Black carbon aerosols plays an important role in the earth's radiative balance and little is known of their concentrations, distributions, source strength, and especially the aerosol chemistry of the developing world. The present study addresses the impact of back carbon aerosols on different atmospheric species like CO and tropospheric ozone over an urban environment, namely Hyderabad, India. Ozone concentration varies from 14 to 63 ppbv over the study area. Diurnal variations of ozone suggest that ozone concentration starts increasing gradually after sunrise, attaining a maximum value by evening time and decreasing gradually thereafter. Black carbon (BC) aerosol mass concentrations varies from 1471 to 11,175 ng m⁻³. The diurnal variations of BC suggest that the concentrations are increased by a factor of 2 during morning (06:00–09:00 h) and evening hours (18:00 to 22:00 h) compared to afternoon hours. Positive correlation has been observed between BC and CO (r²=0.74) with an average slope of 6.4×10⁻³ g BC/g CO. The slope between black carbon aerosol mass concentration and tropospheric ozone suggests that every 1 μg m⁻³ increase in black carbon aerosol mass concentration causes a 3.5 μg m⁻³ reduction in tropospheric ozone. The results have been discussed in detail in the paper.     

An Aerosol Model of the Marine and Coastal Atmospheric Surface Layer

We present a microphysical model for the surface layer marine and coastal atmospheric aerosols that is based on long-term observations of size distributions for 0.01–100 µm particles. The fundamental feature of the model is a parameterization of amplitudes and widths for aerosol modes of the aerosol size distribution function (ASDF) as functions of fetch and wind speed. The shape of ASDF and its dependence on meteorological parameters, height above sea level (H), fetch (X), wind speed (U) and relative humidity (RH), are investigated. At present, the model covers the ranges H = 0–25 m, U?=?3–18 km s^?1, X?≤?120 km and RH?=?40–98%.

The latest version of the Marine Aerosol Extinction Profiles model (MaexPro) is described and applied to the computation and analysis of the spectral profiles of aerosol extinction coefficients α(λ) in the wavelength band λ?=?0.2–12 µm. MaexPro is based on the aforementioned aerosol model assuming spherically shaped aerosol particles and the well-known Mie theory.

The spectral profiles of α(λ) calculated by MaexPro are in good agreement with observational data and the numerical results obtained from the Navy Aerosol Model (NAM) and the Advanced Navy Aerosol Model (ANAM). Moreover, MaexPro was found to be an accurate and reliable tool for investigating the optical properties of atmospheric aerosols.     

A GCM study of future climate response to aerosol pollution reductions

We use the global atmospheric GCM aerosol model ECHAM5-HAM to asses possible impacts of future air pollution mitigation strategies on climate. Air quality control strategies focus on the reduction of aerosol emissions. Here we investigate the extreme case of a maximum feasible end-of-pipe abatement of aerosols in the near term future (2030) in combination with increasing greenhouse gas (GHG) concentrations. The temperature response of increasing GHG concentrations and reduced aerosol emissions leads to a global annual mean equilibrium temperature response of 2.18 K. When aerosols are maximally abated only in the Industry and Powerplant sector, while other sectors stay with currently enforced regulations, the temperature response is 1.89 K. A maximum feasible abatement applied in the Domestic and Transport sector, while other sectors remain with the current legislation, leads to a temperature response of 1.39 K. Increasing GHG concentrations alone lead to a temperature response of 1.20 K. We also simulate 2–5% increases in global mean precipitation among all scenarios considered, and the hydrological sensitivity is found to be significantly higher for aerosols than for GHGs. Our study, thus highlights the huge potential impact of future air pollution mitigation strategies on climate and supports the need for urgent GHG emission reductions. GHG and aerosol forcings are not independent as both affect and are influenced by changes in the hydrological cycle. However, within the given range of changes in aerosol emissions and GHG concentrations considered in this study, the climate response towards increasing GHG concentrations and decreasing aerosols emissions is additive.     

不同污染条件下气溶胶对短波辐射通量影响的模拟研究

将高光谱分辨率的气溶胶光学参数化方案应用于高精度的辐射传输模式BCC_RAD（974带）中,研究不同污染状况下气溶胶在地表与近地层大气中造成的直接辐射强迫与辐射强迫效率。发现气溶胶在地表产生的直接辐射强迫为负,在近地层大气中产生的直接辐射强迫为正,且随气溶胶浓度的升高变大,说明大气气溶胶的含量越高,单位气溶胶光学厚度产生的直接辐射强迫越大。将短波划分为3个波段:紫外、可见光和近红外,发现在紫外、可见光和近红外波段中,不同污染状况下气溶胶在地表造成的直接辐射强迫范围分别为:-1.36—-13.66、-3.03—-32.41和-2.74—-28.62 W/m2,在近地层大气中产生的直接辐射强迫范围分别为0.44—4.26、0.99—9.80和0.93—8.87 W/m2。通过进一步对比自然和人为气溶胶的影响,发现人为气溶胶在地表和大气层顶产生的负直接辐射强迫以及对整层和近地面大气造成的正直接辐射强迫均大于自然气溶胶的影响,且上述两种排放源的气溶胶对整层大气辐射收支的影响主要集中在800 hPa高度以下的大气中。按照地表直接辐射强迫大小来分析不同种类气溶胶的影响,结果为硫酸盐>有机碳>黑碳>海盐>沙尘;按照近地层大气直接辐射强迫大小排序则为黑碳>有机碳>沙尘>海盐>硫酸盐。最后,通过分析散射型气溶胶与吸收型气溶胶对辐射通量的影响,还探究了大气中散射与吸收过程的异同。      

北方局地夏末气溶胶光学特性综合观测分析

本文对中国北方相近地理经度不同纬度的三个试验点（内蒙草原生态定位站、北京、新乡）夏末季节大气气溶胶特性进行了地面粒子计数和整层光学遥感等综合观测。分析结果表明，这三个试验点地面和整层气溶胶数浓度通常有内蒙较小，北京居中，新乡最大的特征。文中提出了浓度比这个参量，它可以定量描述地面源气溶胶对整层大气气溶胶的相对贡献。据此分析可知内蒙地面源较弱，与该地区人类活动稀少相对应。由浓度比推测，新乡除近地面城市空气污染较严重外，滨临的黄河河面水汽蒸发作用也是促成气溶胶浓度增大的原因。     

RADIATIVE CHARACTERISTICS OF AEROSOLS AT GOLMUD ON THE TIBETAN PLATEAU

The characteristics of atmospheric aerosols in the Golmud desert over the Tibetan (Qinghai-Xizang) Plateau are investigated using the measurements made during the QXPMEX-79.Using spectroscopic observations at the surface and satellite data,the aerosol optical depth is calculated,from which the aerosol size distribution is worked out by means of an inversion method.The effects of vertical distribution of aerosols on irradiance and heating rate profiles are investigated using radiation models in conjunction with the assumption of three idealized aerosol profiles.The effect of aerosols on solar irradiance at the surface is also investigated and the results are compared with the observations.It is shown that the solar irradiance can be reduced by up to 100 W m^-2 in the presence of aerosols,and the heating rate can be increased by 1 Kd^-1.     

Impact of Different Aerosols on the Evolution of the Atmospheric Boundary Layer

The present work analyzes the effect of aerosols on the evolution of the atmospheric boundary layer (ABL) over Shangdianzi in Beijing.A one-dimensional ABL model and a radiative transfer scheme are incorporated to develop the structure of the ABL.The diurnal variation of the atmospheric radiative budget,atmospheric heating rate,sensible and latent heat fluxes,surface and the 2 m air temperatures as well as the ABL height,and its perturbations due to the aerosols with different single-scattering albedo (SSA) are studied by comparing the aerosol-laden atmosphere to the clean atmosphere.The results show that the absorbing aerosols cause less reduction in surface evaporation relative to that by scatting aerosols,and both surface temperature and 2 m temperature decrease from the clean atmosphere to the aerosol-laden atmosphere.The greater the aerosol absorption,the more stable the surface layer.After 12:00 am,the 2 m temperature increases for strong absorption aerosols.In the meantime,there is a slight decrease in the 2 m temperature for purely scattering aerosols due to radiative cooling.The purely scattering aerosols decrease the ABL temperature and enhance the capping inversion,further reducing the ABL height.     

大气气溶胶研究的前沿问题

从4个方面对大气气溶胶研究的前沿问题作了总结和分析：气溶胶的基本特征、气溶胶的气候效应、沙尘气溶胶以及气溶胶对健康环境的影响。介绍了当前国际上有关的大气气溶胶研究计划,讨论了未来大气气溶胶研究的主要领域及研究方向。     

Observation-based Estimation of Aerosol-induced Reduction of Planetary Boundary Layer Height

Radiative aerosols are known to influence the surface energy budget and hence the evolution of the planetary boundary layer. In this study, we develop a method to estimate the aerosol-induced reduction in the planetary boundary layer height(PBLH) based on two years of ground-based measurements at a site, the Station for Observing Regional Processes of the Earth System(SORPES), at Nanjing University, China, and radiosonde data from the meteorological station of Nanjing. The observations show that increased aerosol loads lead to a mean decrease of 67.1 W m-2for downward shortwave radiation(DSR) and a mean increase of 19.2 W m-2for downward longwave radiation(DLR), as well as a mean decrease of 9.6W m-2for the surface sensible heat flux(SHF) in the daytime. The relative variations of DSR, DLR and SHF are shown as a function of the increment of column mass concentration of particulate matter(PM2.5). High aerosol loading can significantly increase the atmospheric stability in the planetary boundary layer during both daytime and nighttime. Based on the statistical relationship between SHF and PM2.5column mass concentrations, the SHF under clean atmospheric conditions(same as the background days) is derived. In this case, the derived SHF, together with observed SHF, are then used to estimate changes in the PBLH related to aerosols. Our results suggest that the PBLH decreases more rapidly with increasing aerosol loading at high aerosol loading. When the daytime mean column mass concentration of PM2.5reaches 200 mg m-2, the decrease in the PBLH at 1600 LST(local standard time) is about 450 m.     

Aerosol direct forcing of the summer Indian monsoon as simulated by the NCAR CAM3

In this study, the effects of aerosols on the simulation of the Indian monsoon by the NCAR Community Atmosphere Model CAM3 are measured and investigated. Monthly mean 3D mass concentrations of soil dust, black and organic carbons, sulfate, and sea salt, as output from the GOCART model, are interpolated to mid-month values and to the horizontal and vertical grids of CAM3. With these mid-month aerosol concentrations, CAM3 is run for a period of approximately 16 months, allowing for one complete episode of the Indian monsoon. Responses to the aerosols are measured by comparing the mean of an ensemble of aerosol-induced monsoon simulations to the mean of an ensemble of CAM3 simulations in which aerosols are omitted, following the method of Lau et al. (2006) in their experiment with the NASA finite volume general circulation model. Additionally, an ensemble of simulations of CAM3 using climatological mid-month aerosol concentrations from the MATCH model is composed for comparison. Results of this experiment indicate that the inclusion of aerosols results in drops in surface temperature and increases in precipitation over central India during the pre-monsoon months of March, April, and May. The presence of aerosols induces tropospheric shortwave heating over central India, which destabilizes the atmosphere for enhanced convection and precipitation. Reduced shortwave heating and enhanced evaporation at the surface during April and May results in reduced terrestrial emission to cool the lower troposphere, relative to simulations with no aerosols. This effect weakens the near-surface cyclonic circulation and, consequently, has a negative feedback on precipitation during the active monsoon months of June and July.     

北京地区气溶胶粒度谱分布初步研究

本文对北京地区气溶胶数浓度及其诸分布特征进行了初步研究。重点探讨了气溶胶数浓度分布与相对湿度的关系。研究结果表明，气溶胶浓度和谱分布存在明显的日变化和逐日变化，并在很大程度上受空气相对湿度和理查森数影响。     

非洲地区大气气溶胶光学厚度时空变化及亚速尔高压对沙尘越大西洋传输的影响

研究了非洲地区大气气溶胶光学厚度（AOD）的时空变化及沙尘气溶胶越大西洋海区的传输。结果表明：1）源于撒哈拉沙漠的沙尘及其随赤道东风向西输送使得沙尘气溶胶成为非洲沙漠地区和紧邻的大西洋海区的主要气溶胶组分;AOD高值区和沙尘气溶胶光学厚度高值区在1—7月随赤道辐合带北移同步向北移动,而在8—12月则向南回撤。2）刚果盆地大气气溶胶主要为热带雨林和稀树草原排放的有机碳（OC）和黑碳（BC）气溶胶;其中与生物质燃烧源排放有关的OC、BC高值主要集中在干季（6—9月）的后半段（8—9月）;而生物源OC排放全年连续,其排放峰值出现于雨季开始时;生物质燃烧排放高值期与生物源排放高值期前后相继,形成干季（尤其是后半段）时期的OC、BC光学厚度高值。3）亚马逊河入海口地区主要气溶胶组分为海盐气溶胶,9—11月该区风力输送增强,风向由东南风转变为东风,海盐进入亚马逊河入海口处,形成AOD和海盐气溶胶光学厚度高值区。4）撒哈拉沙漠沙尘气溶胶向大西洋传输的偏北月份为7—9月、偏南月份为1—3月;2000—2016年海区沙尘气溶胶的传输路径存在向南移动的变化趋势,与同期亚速尔高压的增强和沙尘传输路径以北北风分量的增强以及赤道辐合带的移动一致。上述研究结果揭示了利用大气气溶胶时空变化特征反映区域大气环流和气候变化的可能性。     

Aerosol physical characteristics at Bhubaneswar, East coast of India

Physical characterization of atmospheric aerosols was carried out using various equipments like Grimm's spectrophotometer, Aetholometer and Microtops-II at Bhubaneswar, a coastal city in the east coast of India. Meteorological parameters were recorded on-line with an automatic weather station, which showed weather relatively free from extreme events with high humidity during the period. The pre-monsoon months showed an increase in aerosol mass in the higher size ranges. The black carbon (BC) showed maximum values during winter which may be due to various anthropogenic activities like biomass burning and forest fire as well as dry conditions conducive to transport from far off places. The α values representing aerosol size distribution and β values showing the total aerosol concentration in vertical air column rose simultaneously in pre-monsoon months to attain maximum values during February–March 2008. The AOD was also correlated with PM-10 and BC concentrations.     

Comparison between urban aerosol products retrieved from collocated Cimel and Prede Sun/sky radiometers at Pune, India

To comprehend the characteristics of heterogeneous aerosols, apart from some thematic multi-institutional, multi-platform and multi-parameter campaigns conducted at several places over the globe, presently two major ground-based networks, involving Cimel (AERONET) and Prede (SKYNET) Sun/sky photometers/radiometers have been in progress. In this paper, we report the results of a study that has been undertaken to compare the performance and data products of Cimel and Prede instruments, which were operated concurrently for a period of about 2 years, at the Indian Institute of Tropical Meteorology, Pune, India. The results show a good agreement in the direct Sun observations (aerosol optical depth). The results are also substantiated by making comparison with surface-level black carbon aerosol mass concentration, apart from comparison of other parameters. With regard to the retrieved products such as aerosol size distribution, Prede shows more or less equal concentration of fine mode and relatively more concentration of coarse mode aerosol as compared to those measured by the Cimel. Moreover, the single scattering albedo values measured by the Prede overestimate those observed by the Cimel. These deviations are found to be primarily due to the nature of aerosol loading (turbidity) in the sensing region which is sensitive to the data retrieval techniques including model assumptions employed in both networks. The results of the present study are found useful for multidimensional mapping of aerosol characteristics by integrating the products from both AERONET and SKYNET monitoring stations and thereby help understanding better the impact of aerosols on climate.     

The effects of black carbon and sulphate aerosols in China regions on East Asia monsoons

In this paper, we examine the direct effects of sulphate and black carbon (BC) aerosols in China on East Asia monsoons and its precipitation processes by using the Community Atmosphere Model (CAM) 3.0 model. It is demonstrated that sulphate and BC aerosols in China both have the effects to weaken East Asia monsoons in both summer and winter seasons. However, they certainly differ from each other in affecting vertical structures of temperature and atmospheric circulations. Their differences are expected because of their distinct optical properties, that is, scattering versus absorbing. Even for a single type of aerosol, its effects on temperature structures and atmospheric circulations are largely season-dependent. Applications of T -test on our results indicate that forcing from BC aerosols over China is relatively weak and limited. It is also evident from our results that the effects of synthetic aerosols (sulphate and BC together) on monsoons are not simply a linear summation between these two types of aerosols. Instead, they are determined by their integrated optical properties. Synthetic aerosols to a large degree resemble effects of sulphate aerosols. This implies a likely scattering property for the integration of BC and sulphate aerosols in China.     

2008年北京奥运会期间大气气溶胶物理特征分析

应用MODIS卫星的气溶胶产品资料和地面的光学粒子计数器的资料,对比分析了北京地区2006、2007、2008年7～9月的气溶胶光学厚度、细粒子光学厚度、Angstrom指数、气溶胶粒子数浓度谱及体积谱,发现2008年北京奥运会期间(7月20日～9月20日)的气溶胶光学厚度比2006、2007年同期明显降低,气溶胶细模态光学厚度占总光学厚度的比上升,Angstrom指数上升,气溶胶细粒子数浓度没有明显相对变化,而粗粒子数浓度则减少约50%.利用大气标高,将MODIS反演的气溶胶柱的质量浓度转化为地面气溶胶质量浓度.用粒子计数器得到的体积谱,在假定气溶胶粒子密度的情况下,计算出其质量浓度.将这两种方法得到的气溶胶质量浓度与国家环境保护部公布的空气质量指数换算得到的可吸入颗粒物(PM10)质量浓度进行比较.结果表明:北京奥运期间空气质量总体达到了国家二级空气质量标准;与2006、2007年同期相比,2008年气溶胶PM10质量浓度明显下降,而这主要是由气溶胶粗粒子的减少引起的.     

Radiative effect of black carbon aerosol on seasonal variation in snow depth in the Northern-Hemisphere

In this research, we studied the effects of black carbon (BC) aerosol radiative forcing on seasonal variation in the Northern Hemisphere (NH) using numerical simulations with the NASA finite-volume General Circulation Model (fvGCM) forced with monthly varying three-dimensional aerosol distributions from the Goddard Ozone Chemistry Aerosol Radiation and Transport Model (GOCART). The results show that atmospheric warming due to black carbon aerosols subsequently warm the atmosphere and land surfaces, especially those over Eurasia. As a result, the snow depth in Eurasia was greatly reduced in late winter and spring, and the reduction in snow cover decreased the surface albedo. Our surface energy balance analysis shows that the surface warming due to aerosol absorption causes early snow melting and further increases surface-atmosphere warming through snow/ice albedo feedback. Therefore, BC aerosol forcing may be an important factor affecting the snow/ice albedo in the NH.