CAM30模式中黑碳及硫酸盐气溶胶浓度变化 对东亚春季气候的影响研究

本文采用CAM30 模式研究东亚地区各种气溶胶浓度增加后对于东亚春季各气候要素,尤其是对降水和春季风场的影响。在模式中通过分别对区域（20～50 °N,100～150 °E）内黑碳气溶胶浓度单独加倍、硫酸盐气溶胶浓度单独加倍、两种气溶胶浓度同时加倍的实验方法,探讨不同气溶胶浓度变化在东亚春季气候变化中的具体作用。结果表明：在春季,3种气溶胶浓度增加方式都使得东亚地区表现出降水中南部减少北部增加,低层大气西南风异常以及地面温度南部增加北部减少。通过对110～120 °E的断面分析发现,硫酸盐与黑碳气溶胶在春季首先影响约800 hPa以上大气的温度并通过不同的动力机制影响东亚地区的风场,风场的改变进而导致了云量和降水在东亚北方地区增多而中南部地区减少,并最终使得地面温度表现出东亚中南部地区增温而北方地区相对降温的特征。     

CAM3.0模式中东亚气溶胶浓度变化的直接效应及全球海面温度年代际变化对东亚夏季降水的影响研究

利用CAM3.0气候模式模拟研究东亚地区气溶胶浓度增长以及1976/1977年前后发生的海温年代际变化对东亚夏季降水场的影响及其机制。采用四组试验:即对东亚区域(100~150 °E,20~50 °N)分别进行的单独加倍黑碳气溶胶浓度、单独加倍硫酸盐气溶胶浓度、同时加倍这两种气溶胶浓度的三组关于气溶胶直接气候效应的试验及全球海温在1976/1977前后发生变化的海温年代际变化试验,来比较、探讨海温年代际变化和东亚地区气溶胶浓度增加对东亚夏季降水的影响机制。结果表明,无论是海温年代际变化还是各种气溶胶的浓度加倍,都能导致我国出现长江以北地区降水减少-东南沿海地区降水增加的“南涝北旱”的降水异常分布型。但两者在洋面上空降水的迥异表现及东亚低层风场的不同变化,显示其具有不同的异常降水机制。比较三类气溶胶浓度增加的试验结果发现:在单独硫酸盐气溶胶浓度增加试验中,东亚中部出现最显著的中下层大气降温、异常下沉气流以及降水减少;而在黑碳气溶胶试验中,出现在东亚中部的异常下沉气流强度减弱且位置偏南;在同时增加两类气溶胶浓度时,降水异常分布与单独黑碳气溶胶浓度增加所导致的降水异常相近,但强度减小。      

人为气溶胶对中国东部冬季风影响的模拟研究

采用美国国家大气研究中心(NCAR)的公共大气模式CAM5.1研究了人为气溶胶排放增加对中国东部冬季风的影响,同时通过对比中国东部地区不同人为气溶胶排放源的敏感性试验结果,探讨了人为硫酸盐、黑碳及总人为气溶胶(硫酸盐+黑碳)增加对东亚冬季风的影响。结果表明:冬季硫酸盐气溶胶排放增加的直接和第一间接效应减少了到达地表的短波辐射通量,引起了陆地地表和对流层低层降温,海平面气压升高,增加了海陆间气压梯度,使得东亚冬季风增强。其第二间接效应导致中国南部大尺度降水率减少;黑碳气溶胶排放增加导致到达地表的短波辐射通量减少和大气中短波辐射通量增加,其半直接效应部分抵消了直接效应,故地表温度变化微小且不显著。加热的对流层低层导致中国南部对流活动和对流降水率增加;总人为气溶胶排放增加导致的大气温度变化表现为弱的降温作用,引起中国北部对流和大尺度降水率减少,而南部对流降水率增加。总人为气溶胶和黑碳气溶胶排放增加是导致中国北(南)部的东亚冬季风增强(减弱)的重要因素。     

东亚地区人为气溶胶直接辐射强迫及其气候效应的数值模拟

利用耦合化学过程的区域气候模式RegCM3,模拟研究3种主要人为排放气溶胶(硫酸盐、黑碳、有机碳)对东亚区域气候的影响.计算分析近20 a来3种气溶胶的时空分布、综合辐射强迫作用及其对地面气温和降水的影响.模拟结果表明:3种气溶胶冬夏季分布有所不同,冬季气溶胶大值区主要分布在南方地区,而夏季大值区北移;气溶胶短波辐射强迫在大气层顶和地面均为负值;气溶胶的加入对东亚地区地表气温有明显影响,冬季降温中心位于四川盆地,夏季降温大值区位于华北地区.气溶胶直接气候效应使得冬季东亚大部分地区降水减少,夏季东亚地区降水与中国南方地区夏季气溶胶浓度有较好的相关关系,中国东部雨带有南移趋势.     

近22a人为气溶胶对东亚地区夏季风环流影响的数值模拟研究

运用区域气候模式RegCM3耦合入一个化学过程,对东亚地区三类人为排放气溶胶（硫酸盐、黑碳和有机碳）的时空分布特征及其对夏季风环流的影响进行了数值模拟研究.模拟结果显示,气溶胶的引入会引起东亚地区夏季850 hPa风场发生改变,我国江淮以东洋面上空出现了一个气旋式距平环流中心,中心以西的偏北风气流将削弱东亚地区夏季西南季风.通过讨论春季中国地区气溶胶浓度与夏季东亚地区850 hPa经向风的时滞关系,以及夏季中国地区气溶胶浓度与同期东亚地区850 hPa经向风的关系,可以发现,春、夏季中国地区气溶胶浓度均与夏季东亚地区850hPa经向风有很好的负相关关系,当春季中国北方和夏季中国南方地区气溶胶浓度增加时,中国东部地区夏季偏南季风减弱.这可能与气溶胶改变了大气层顶和地表的辐射强迫,进而引起了海陆气压差异和位势高度场的变化有关.     

近22 a人为气溶胶对东亚地区夏季风环流影响的数值模拟研究

运用区域气候模式RegCM3耦合入一个化学过程,对东亚地区三类人为排放气溶胶（硫酸盐、黑碳和有机碳）的时空分布特征及其对夏季风环流的影响进行了数值模拟研究。模拟结果显示,气溶胶的引入会引起东亚地区夏季850 hPa风场发生改变,我国江淮以东洋面上空出现了一个气旋式距平环流中心,中心以西的偏北风气流将削弱东亚地区夏季西南季风。通过讨论春季中国地区气溶胶浓度与夏季东亚地区850 hPa经向风的时滞关系,以及夏季中国地区气溶胶浓度与同期东亚地区850 hPa经向风的关系,可以发现,春、夏季中国地区气溶胶浓度均与夏季东亚地区850 hPa经向风有很好的负相关关系,当春季中国北方和夏季中国南方地区气溶胶浓度增加时,中国东部地区夏季偏南季风减弱。这可能与气溶胶改变了大气层顶和地表的辐射强迫,进而引起了海陆气压差异和位势高度场的变化有关。     

基于国际大气化学—气候模式比较计划模式数据评估未来气候变化对中国东部气溶胶浓度的影响

气候变化引起的地面气溶胶浓度变化与区域空气质量密切相关。本文利用“国际大气化学—气候模式比较计划”（Atmospheric Chemistry and Climate Model Intercomparison Project, ACCMIP）中4个模式的试验数据分析了RCP8.5情景下2000~2100年气候变化对中国气溶胶浓度的影响。结果显示,在人为气溶胶排放固定在2000年、仅考虑气候变化的影响时,2000~2100年气候变化导致中国北部地区（31°N~45°N, 105°E~122°E）硫酸盐、有机碳和黑碳气溶胶分别增加28%、21%和9%,硝酸盐气溶胶在中国东部地区减少30%。气候变化对细颗粒物（PM_2.5）浓度的影响有显著的季节变化特征,冬季PM_2.5浓度在中国东部减少15%,这主要是由硝酸盐气溶胶在冬季的显著减少造成的;夏季PM_2.5浓度在中国北部地区增加16%,而长江以南地区减少为9%,这可能与模式模拟的未来东亚夏季风环流的增强有关。     

中国区域气溶胶对东亚夏季风的可能影响(Ⅱ)：黑碳气溶胶及其与硫酸盐气溶胶的综合影响

 利用NCAR的新一代GCM CAM3.0模式耦合一个气溶胶同化系统,研究了中国区域黑碳气溶胶的直接气候效应。结果显示,中国区域黑碳气溶胶引起全球平均辐射强迫为0.13 W/m2,导致除了青藏高原和广西以外的中国大部分地区降温,其中东北、四川和内蒙古中北部降温最显著。由此造成海陆温差缩小,气压差降低,从而总体上使东亚夏季风减弱。但与硫酸盐气溶胶的影响相比,黑碳气溶胶使季风减弱的程度较小,长江中下游地区的降水有所增加。黑碳气溶胶加强了中国东南部地区的对流活动,这与硫酸盐气溶胶的作用相反。同时,探讨了中国区域硫酸盐和黑碳气溶胶的综合直接气候效应。结果表明,硫酸盐和黑碳气溶胶的综合作用与仅有硫酸盐气溶胶的情形十分相似,降水变化的区域也和硫酸盐的保持一致。     

中国区域气溶胶对东亚夏季风的可能影响(Ⅱ)：黑碳气溶胶及其与硫酸盐气溶胶的综合影响

利用NCAR的新一代GCM CAM3.0模式耦合一个气溶胶同化系统,研究了中国区域黑碳气溶胶的直接气候效应。结果显示,中国区域黑碳气溶胶引起全球平均辐射强迫为0.13 W/m2,导致除了青藏高原和广西以外的中国大部分地区降温,其中东北、四川和内蒙古中北部降温最显著。由此造成海陆温差缩小,气压差降低,从而总体上使东亚夏季风减弱。但与硫酸盐气溶胶的影响相比,黑碳气溶胶使季风减弱的程度较小,长江中下游地区的降水有所增加。黑碳气溶胶加强了中国东南部地区的对流活动,这与硫酸盐气溶胶的作用相反。同时,探讨了中国区域硫酸盐和黑碳气溶胶的综合直接气候效应。结果表明,硫酸盐和黑碳气溶胶的综合作用与仅有硫酸盐气溶胶的情形十分相似,降水变化的区域也和硫酸盐的保持一致。     

黑碳气溶胶对我国区域气候影响的数值模拟

利用区域气候模式RegCM3模拟研究了黑碳气溶胶对我国区域气候的影响。以2000年1、4、7、10月为代表,计算分析了黑碳气溶胶的辐射强迫作用、对大气温度和降水的影响及其季节变化特征。模拟结果显示：黑碳气溶胶在大气层顶产生正的辐射强迫,在地表产生负的辐射强迫;黑碳气溶胶的加入使中国大陆地区地面温度发生明显变化,并呈现显著的季节特征,即1月大部分地区的地面温度均有升高;7月北方增温、南方降温;4月和10月地面温度的变化不明显。模拟结果也表明,黑碳气溶胶的排放使我国长江中下游等南方地区夏季降水增加,而北方部分地区降水减少。     

Identification of Aerosol Types and Their Optical Properties in the North China Plain Based on Long-Term AERONET Data

Characterization of aerosols is required to reduce uncertainties in satellite retrievals of global aerosols and for modeling the effects of these aerosols on climate.Aerosols in the North China Plain(NCP) are complex,which provides a good opportunity to study key aerosol optical properties for various aerosol types.A cluster analysis of key optical properties obtained from Aerosol Robotic Network(AERONET) data in Beijing and Xianghe during 2001-11 was performed to identify dominant aerosol types and their associated optical properties.Five dominant aerosol types were identified.The results show that the urban/industrial aerosol of moderate absorption was dominant in the region and that this type varied little with season.Urban/industrial aerosol of weak absorption was the next most common type and mainly occurs in summer,followed by that strong aerosols occurring mainly in winter.All were predominantly fine mode particles.Mineral dust(MD) and polluted dust(PD) occurred mainly in spring,followed by winter,and their absorption decreased with wavelength.In addition,aerosol dynamics and optical parameters such as refractive index and asymmetry factor were examined.Results show that the size of coarse mode particles decreased with AOD indicating the domination of external mixing between aerosols.     

The Global Distribution of Secondary Particulate Matter in a 3-D Lagrangian Chemistry Transport Model

A global 3-D Lagrangian chemistry-transport model STOCHEM is used to describe the tropospheric distributions of four components of the secondary atmospheric aerosol: nitrate, sulphate, ammonium and organic compounds. The model describes the detailed chemistry of the formation of the acid precursors from the oxidation of SO₂, DMS, NO_x, NH₃ and terpenes and their uptake into the aerosol. Model results are compared in some detail with the available surface observations. Comparisons are made between the global budgets and burdens found in other modelling studies. The global distributions of the total mass of secondary aerosols have been estimated for the pre-industrial, present day and 2030 emissions and large changes have been estimated in the mass fractions of the different secondary aerosol components.     

中国气溶胶研究进展

结合近年来中国气溶胶研究的现状, 分别对气溶胶的基本特征、气溶胶的气候效应、沙尘气溶胶以及与气溶胶有关的其它研究等四部分内容作了总结和分析。     

Sulfate and methanesulfonate in the maritime aerosol at Cape Grim,Tasmania

High-volume aerosol filters, exposed in maritime air masses at Cape Grim since late 1976, were analysed for excess sulfate (not of seasalt origin) and methanesulfonate. The mean concentrations (standard errors) of 2.80(0.59) and 0.176(0.027) nmole/m³ respectively are about half those reported in a recent study of aerosol samples from various locations in the Atlantic and Pacific oceans.Methanesulfonate concentration varied seasonally by at least an order of magnitude with a summer maximum and winter minimum. No comparable cycle was found for excess sulfate.     

A review of global stratospheric aerosol: Measurements, importance, life cycle, and local stratospheric aerosol

Stratospheric aerosol, noted after large volcanic eruptions since at least the late 1800s, were first measured in the late 1950s, with the modern continuous record beginning in the 1970s. Stratospheric aerosol, both volcanic and non-volcanic are sulfuric acid droplets with radii (concentrations) on the order of 0.1–0.5 µm (0.5–0.005 cm^− 3), increasing by factors of 2–4 (10–10³) after large volcanic eruptions. The source of the sulfur for the aerosol is either through direct injection from sulfur-rich volcanic eruptions, or from tropical injection of tropospheric air containing OCS, SO₂, and sulfate particles. The life cycle of non-volcanic stratospheric aerosol, consisting of photo-dissociation and oxidation of sulfur source gases, nucleation/condensation in the tropics, transport pole-ward and downward in the global planetary wave driven tropical pump, leads to a quasi steady state relative maximum in particle number concentration at around 20 km in the mid latitudes. Stratospheric aerosol have significant impacts on the Earth's radiation balance for several years following volcanic eruptions. Away from large eruptions, the direct radiation impact is small and well characterized; however, these particles also may play a role in the nucleation of near tropopause cirrus, and thus indirectly affect radiation. Stratospheric aerosol play a larger role in the chemical, particularly ozone, balance of the stratosphere. In the mid latitudes they interact with both nitrous oxides and chlorine reservoirs, thus indirectly affecting ozone. In the polar regions they provide condensation sites for polar stratospheric clouds which then provide the surfaces necessary to convert inactive to active chlorine leading to polar ozone loss. Until the mid 1990s the modern record has been dominated by three large sulfur-rich eruptions: Fuego (1974), El Chichón (1982) and Pinatubo (1991), thus definitive conclusions concerning the trend of non-volcanic stratospheric aerosol could only recently be made. Although anthropogenic emissions of SO₂ have changed somewhat over the past 30 years, the measurements during volcanically quiescent periods indicate no long term trend in non-volcanic stratospheric aerosol.     

气溶胶对陆生植物生长的影响研究进展

陆生植物生长过程受太阳辐射、热量、水分、土壤等多重因素的影响,气溶胶粒子通过对太阳辐射的散射和吸收,并作为云凝结核和冰核,改变云的物理特性及生命期对上述环境因子产生影响,进而影响植物的生长。气溶胶的直接影响主要表现为气溶胶覆盖植物叶片,影响植物的呼吸作用、气孔导度及对阳光的利用率等;间接影响主要表现在气溶胶可降低入射太阳辐射量并降低光合作用及净初级生产力,但同时又会增加散射辐射量,增加植物可利用光合有效辐射,产生相互矛盾的结果;气溶胶还通过影响降水和气温,进一步影响植物对光、水、热的利用等方面。气溶胶对植物的生长影响以间接影响为主,直接影响较少。其次,各种大气气溶胶对植物的伤害作用超过大气气溶胶对植物生长促进作用。在人为气溶胶中,硫酸盐、黑碳及粉尘对植物生长以抑制作用为主,而氮化物中氮沉降既可以促进植物生长,含氮气溶胶形成的酸雨及光化学烟雾又会抑制植物生长。自然气溶胶中,火山气溶胶对植物生长产生的影响差异较大,沙尘总体对植物产生不利影响,而生物气溶胶及宇宙尘埃的影响研究还较少。     

Observed changes in aerosol physical and optical properties before and after precipitation events

Precipitation scavenging of aerosol particles is an important removal process in the atmosphere that can change aerosol physical and optical properties. This paper analyzes the changes in aerosol physical and optical properties before and after four rain events using in situ observations of mass concentration, number concentration, particle size distribution, scattering and absorption coefficients of aerosols in June and July 2013 at the Xianghe comprehensive atmospheric observation station in China. The results show the effect of rain scavenging is related to the rain intensity and duration, the wind speed and direction. During the rain events, the temporal variation of aerosol number concentration was consistent with the variation in mass concentration, but their size-resolved scavenging ratios were different. After the rain events, the increase in aerosol mass concentration began with an increase in particles with diameter 0.8 μm [measured using an aerodynamic particle sizer(APS)], and fine particles with diameter 0.1 μm [measured using a scanning mobility particle sizer(SMPS)]. Rainfall was most efficient at removing particles with diameter ～0.6 μm and greater than 3.5 μm. The changes in peak values of the particle number distribution(measured using the SMPS) before and after the rain events reflect the strong scavenging effect on particles within the 100–120 nm size range. The variation patterns of aerosol scattering and absorption coefficients before and after the rain events were similar, but their scavenging ratios differed, which may have been related to the aerosol particle size distribution and chemical composition.     

Chemical Composition of Summertime PM2.5 and Its Relationship to Aerosol Optical Properties in Guangzhou, China

Urban aerosols have a large effect on the deterioration of air quality and the degradation of atmospheric visibility.Characterization of the chemical composition of PM 2.5 and in situ measurements of the optical properties of aerosols were conducted in July 2008 at an urban site in Guangzhou,Southern China.The mean PM 2.5 concentration for the entire period was 53.7±23.2 μg m 3.The mean PM 2.5 concentration (82.7±25.4 μg m 3) on hazy days was roughly two times higher than that on clear days (38.8±8.7 μg m 3).The total water-soluble ion species and the total average carbon accounted for 47.9%±4.3% and 35.2%±4.5%,respectively,of the major components of PM 2.5.The increase of secondary and carbonaceous aerosols,in particular ammonium sulfate,played an important role in the formation of haze pollution.The mean absorption and scattering coefficients and the single scattering albedo over the whole period were 53±20 M m 1,226±111 M m 1,and 0.80±0.04,respectively.PM 2.5 had a high linear correlation with the aerosol extinction coefficient,elemental carbon (EC) was correlated with aerosol absorption,and organic carbon (OC) and SO 4 2 were tightly linked to aerosol scattering.     

塔克拉玛干沙漠地区气溶胶光学厚度卫星遥感产品验证

基于塔克拉玛干沙漠地区地基太阳光度计数据,系统验证2007～2008年星载多角度成像光谱仪(MISR)、中分辨率成像光谱仪(MODIS)和臭氧监测仪(OMI)气溶胶反演产品,旨在定量评估这些产品在我国沙漠地区的气溶胶光学厚度(AOD)反演精度。结果表明:MODIS/AOD的相关系数在4种产品中最高(0.91),OMI/AOD次之(0.87),其次为MISR/AOD(0.84),OMI/UVAI相关系数偏低(0.51)。MISR/AOD均方根误差(0.14)和平均偏差(-0.06)在4种反演产品中最低。与地基观测相比,MISR/AOD、MODIS/AOD系统偏低,OMI/AOD、OMI/UVAI系统偏高。在相同比较条件下(地基观测气溶胶光学厚度值限定在2.0以内),MISR的均方根误差和平均偏差在4种反演产品中最低,且相关系数也较高(0.84)。尽管存在诸多不同,但3种探测器气溶胶反演产品均能较好地展示该地区的气溶胶季节变化。塔克拉玛干沙漠春、夏季AOD较大,秋、冬季AOD相对较小。ngstrm波长指数的结果表明,春季(3～5月)最小(均值为0.11),夏季(6～8月)次之,秋季(9～11月)和冬季(12月至次年2月)较大(均值达到0.61),这表明在春、夏季气溶胶粒子偏大,秋、冬季气溶胶粒子偏小。此外,通过研究2000～2010年AOD年际变化表明,由于塔克拉玛干沙漠地区属于沙尘源区,气溶胶类型较为单一,所以总体来说,变化趋势不是较为明显。从反演结果来看,2003年的气溶胶含量为此10年中最高,年均值达到0.32;2005年的气溶胶含量在这10年中最低,年均值为0.28。     

Comments on ``Direct Radiative Forcing of Anthropogenic Aerosols over Oceans from Satellite Observation"

Previous observational studies have estimated anthropogenic aerosol direct radiative forcing over oceans without due consideration of cloudy-sky aerosols.However,when interaction between clouds and aerosols located below or above the cloud level is taken into account,the aerosol direct radiative forcing is larger by as much as 5 W m-2 in most mid-latitude regions in the Northern Hemisphere.