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。     

Simulated Spatial Distribution and Seasonal Variation of Atmospheric Methane over China: Contributions from Key Sources简

We used the global atmospheric chemical transport model,GEOS-Chem,to simulate the spatial distribution and seasonal variation of surface-layer methane （CH4） in 2004,and quantify the impacts of individual domestic sources and foreign transport on CH4 concentrations over China.Simulated surface-layer CH4 concentrations over China exhibit maximum concentrations in summer and minimum concentrations in spring.The annual mean CH4 concentrations range from 1800 ppb over western China to 2300 ppb over the more populated eastern China.Foreign emissions were found to have large impacts on CH4 concentrations over China,contributing to about 85％ of the CH4 concentrations over western China and about 80％ of those over eastern China.The tagged simulation results showed that coal mining,livestock,and waste are the dominant domestic contributors to CH4 concentrations over China,accounting for 36％,18％,and 16％,respectively,of the annual and national mean increase in CH4 concentration from all domestic emissions.Emissions from rice cultivation were found to make the largest contributions to CH4 concentrations over China in the summer,which is the key factor that leads to the maximum seasonal mean CH4 concentrations in summer.     

ROx Budgets and O3 Formation during Summertime at Xianghe Suburban Site in the North China Plain

Photochemical smog characterized by high concentrations of ozone (O3) is a serious air pollution issue in the North China Plain (NCP) region, especially in summer and autumn. For this study, measurements of O3, nitrogen oxides (NOx), volatile organic compounds (VOCs), carbon monoxide (CO), nitrous acid (HONO), and a number of key physical parameters were taken at a suburban site, Xianghe, in the NCP region during the summer of 2018 in order to better understand the photochemical processes leading to O3 formation and find an optimal way to control O3 pollution. Here, the radical chemistry and O3 photochemical budget based on measurement data from 1-23 July using a chemical box model is investigated. The daytime (0600-1800 LST) average production rate of the primary radicals referred to as ROx (OH + HO2+ RO2) is 3.9 ppbv h-1. HONO photolysis is the largest primary ROx source (41％). Reaction of NO2 + OH is the largest contributor to radical termination (41％), followed by reactions of RO2 + NO2 (26％). The average diurnal maximum O3 production and loss rates are 32.9 ppbv h-1 and 4.3 ppbv h-1, respectively. Sensitivity tests without the HONO constraint lead to decreases in daytime average primary ROx production by 55％ and O3 photochemical production by 42％, highlighting the importance of accurate HONO measurements when quantifying the ROx budget and O3 photochemical production. Considering heterogeneous reactions of trace gases and radicals on aerosols, aerosol uptake of HO2 contributes 11％ to ROx sink, and the daytime average O3 photochemical production decreases by 14％. The O3-NOx-VOCs sensitivity shows that the O3 production at Xianghe during the investigation period is mainly controlled by VOCs.     

Surface Trace Gases at a Rural Site between the Megacities of Beijing and Tianjin

The North China Plain （NCP） has recently faced serious air quality problems as a result of enhanced gas pollutant emissions due to the process of urbanization and rapid economic growth. To explore regional air pollu- tion in the NCP, measurements of surface ozone （O3）, nitrogen oxides （NOx）, and sulfur dioxide （SO2） were car- ried out from May to November 2013 at a rural site （Xianghe） between the twin megacities of Beijing and Tianjin. The highest hourly ozone average was close to 240 ppbv in May, followed by around 160 ppbv in June and July. High ozone episodes were more notable than in 2005 and were mainly associated with air parcels from the city cluster in the hinterland of the polluted NCP to the southwest of the site. For NOx, an important ozone precur- sor, the concentrations ranged from several ppbv to nearly 180 ppbv in the summer and over 400 ppbv in the fall. The occurrence of high NOx concentrations under calm condi- tions indicated that local emissions were dominant in Xianghe. The double-peak diurnal pattern found in NOx concentrations and NO/NOx ratios was probably shaped by local emissions, photochemical removal, and dilution re- sulting from diurnal variations of surface wind speed and the boundary layer height. A pronounced SO2 daytime peak was noted and attributed to downward mixing from an SO2-rich layer above, while the SO2-polluted air mass transported from possible emission sources, which differed between the non-heating （September and October） and heating （November） periods, was thought to be responsible for night-time high concentrations.     

A Modeling Study of Seasonal Variation of Atmospheric Aerosols over East Asia

In this study, a regional air quality model system (RAQMS) was applied to investigate the spatial distributions and seasonal variations of atmospheric aerosols in 2006 over East Asia. Model validations demonstrated that RAQMS was able to reproduce the evolution processes of aerosol components reasonably well. Ground-level PM₁₀ (particles with aerodynamic diameter ≤10 μm) concentrations were highest in spring and lowest in summer and were characterized by three maximum centers: the Taklimakan Desert (～1000 μg m^-3), the Gobi Desert (～400 μg m^-3), and the Huabei Plain (～300 μm^-3) of China. Vertically, high PM₁₀ concentrations ranging from 100 μg m^-3 to 250 μg m^-3 occurred from the surface to an altitude of 6000 m at 30^o--45^oN in spring. In winter, the vertical gradient was so large that most aerosols were restricted in the boundary layer. Both sulfate and ammonium reached their highest concentrations in autumn, while nitrate reached its maximum level in winter. Black carbon and organic carbon aerosol concentrations reached maximums in winter. Soil dust were strongest in spring, whereas sea salt exerted the strongest influence on the coastal regions of eastern China in summer. The estimated burden of anthropogenic aerosols was largest in winter (1621 Gg) and smallest in summer (1040 Gg). The sulfate burden accounted for ～42% of the total anthropogenic aerosol burden. The dust burden was about twice the anthropogenic aerosol burden, implying the potentially important impacts of the natural aerosols on air quality and climate over East Asia.     

Analysis of Air Quality in Eastern China and its Interaction with Other Regions of the World

In this study, we used satellite data (GOME and MOPITT) together with a global chemical-transport-model of atmosphere (MOZART-2) to characterize the chemical/aerosol composition over eastern China. We then estimated the effects of local emissions in China on the chemical budgets in other regions of the world. Likewise, we also investigated the effects of air pollution from other regions on the chemical budget over eastern China. The study shows that the column CO and NO _x concentrations are also high in eastern China. The high CO and NO _x concentrations produce modest levels of O₃ concentrations during summer (about 40 to 50 ppbv) and very low O₃ during winter (about 10 to 20 ppbv) in eastern China. The calculated NO₂ column is fairly consistent from the GOME measurement. The calculated CO column is underestimated from the MOPITT measurement. One of the reasons of the underestimation of the predicted CO is due to a fact that the CO emissions were taken without considering the rapid increase of emissions from 1990 to 2000. The calculated surface O₃ is consistent with the measured values, with strong seasonal variations. However, the measurement is very limited, and more measurements in eastern China will be needed. The column NO₂ has a very strong seasonal variation in eastern China, with the highest concentrations during winter and the lowest concentrations during summer. The cause of this seasonal variability is mainly due to the seasonal changes in the chemical loss of NO _x , which is very high in summer and very low during winter. The effects of the local emissions in China and long-range transport from other regions on the chemical distributions in eastern China are studied. The results show that NO _x concentrations in eastern China are mostly caused by the local emissions in China, especially during the winter. The CO concentration over eastern China is from both the local emissions (30% to 40%) and the transport from other regions. Likewise, the CO emissions in China have an important effect on the other regions of the world, but the effect is limited in the northern hemisphere. The local emissions in China also have an important effect on surface O₃ concentrations. During winter, the local emissions reduce the surface O₃ concentrations by 30 to 50%. During summer, the local emissions produce about 50 to 70% of the O₃ concentration in eastern China.     

基于模式分析一次沙尘暴过程中沙尘表面非均相化学过程对中国地区污染物浓度的影响

利用戈达德对地观测系统（GEOS）提供的再分析气象场GEOS-5驱动的GEOS-Chem模式,模拟中国地区2009年4月22~29日沙尘暴期间沙尘气溶胶表面非均相化学过程对我国污染物的影响。模拟结果表明,沙尘暴期间,全国平均沙尘硝酸盐和沙尘硫酸盐浓度分别为0.2 μg m-3和0.4 μg m-3,占总硝酸盐（非沙尘硝酸盐与沙尘硝酸盐之和）和总硫酸盐（非沙尘硫酸盐与沙尘硫酸盐之和）的24%和10%。我国西部地区沙尘硝酸盐占比（ > 80%）要大于其他地区,而西部地区的沙尘硫酸盐占比则要小于下游地区。考虑非均相化学反应后,沙尘暴期间,全国平均的二氧化硫（SO₂）、硝酸（HNO₃）、臭氧（O₃）、非沙尘硫酸盐、总硫酸盐、非沙尘硝酸盐、总硝酸盐、NH₃、总铵盐浓度变化量分别为-7%、-15%、-2%、-8%、3%、-2%、14%、21%、-5%。     

Impacts of Future NOx and CO Emissions on Regional Chemistry and Climate over Eastern China

A coupled chemical/dynamical model (SOCOL-SOlar Climate Ozone Links) is applied to study the impacts of future enhanced CO and NOx emissions over eastern China on regional chemistry and climate. The result shows that the increase of CO and NOx emissions has significant effects on regional chemistry, including NOx, CO, O₃, and OH concentrations. During winter, the CO concentration is uniformly increased in the northern hemisphere by about 10 ppbv. During summer, the increase of CO has a regional distribution. The change in O₃, concentrations near eastern China has both strong seasonal and spatial variations. During winter, the surface O₃, concentrations decrease by about 2 ppbv, while during summer they increase by about 2 ppbv in eastern China. The changes of CO, NOx, and O₃, induce important impacts on OH concentrations. The changes in chemistry, especially O₃, induce important effects on regional climate. The analysis suggests that during winter, the surface temperature decreases and air pressure increases in central-eastern China. The changes of temperature and pressure produce decreases in vertical velocity. We should mention that the model resolution is coarse, and the calculated concentrations are generally underestimated when they are compared to measured results. However, because this model is a coupled dynamical/chemical model, it can provide some useful insights regarding the climate impacts due to changes in air pollutant emissions.     

Measurements of Trace Substances in the Arctic Troposphere as Potential Precursors and Constituents of Arctic Haze

During two measuring campaigns in early spring 1994 and 1995 (March/April) and one campaign in summer 1994, measurements of ozone, PAN, sulfur dioxide, nitric acid, and particulate nitrate, sulfate, and ammonium (only 1995) were recorded in the Arctic. Observations were made by aircraft at various sites in the eastern and western Arctic. Ozone concentrations showed a steady increase with altitude both in spring and summer. During five flights in springtime, low ozone events (LOEs) could be observed near the surface and up to altitudes of 2000 m. SO₂ background concentrations, ranging from detection limit (0.5 nmol/m³) to 5 nmol/m³, were observed during both spring and summer. Distinct maxima up to 55 nmol/m³ in lower altitudes were only obtained in springtime. Concentrations of the organic nitrate PAN were within a similar range as those of the inorganic nitrate HNO₃ during spring campaigns. In contrast, concentrations of particulate nitrate were one half an order of magnitude lower. HNO₃ concentrations increased significantly with altitude. Evidently, HNO₃ was intruded from the stratosphere into the troposphere. Sulfate concentrations ranged between 5 and 30 nmol/m³; ammonium concentrations were obtained within a range from 10 to 50 nmol/m³.     

春季中国东部气溶胶化学组成及其分布的模拟研究

本文利用区域空气质量模式RAQMS（Regional Air Quality Model System）,对2009年春季中国东部气溶胶主要化学成分及其分布进行了模拟研究。与泰山站观测资料的对比结果显示,模式能比较合理地反映气溶胶浓度的逐日变化特征。整体上,模式对无机盐气溶胶的模拟好,分别高估和低估黑碳和有机碳气溶胶浓度,其原因与排放源、二次有机气溶胶化学机制和模式分辨率的不确定性有关。模拟结果显示,春季气溶胶浓度高值主要集中于华北、四川东部、长江中下游等地区。受东南亚生物质燃烧和大气输送的影响,中国的云南和广西等地区有机碳浓度高于中国其他地区。中国西北部沙尘浓度较高,而且向东输送并影响到中国东部和南方部分地区。中国东部的华北、四川东部、长江中下游等地PM_2.5（空气动力学直径在2.5微米以下的颗粒物）污染严重,4月平均PM_2.5浓度超过了我国日平均PM_2.5浓度限值。中国东部泰山站的观测和模拟结果都显示近地面硝酸盐浓度超过硫酸盐,中国北部对流层中硝酸盐的柱含量也大于硫酸盐,而在中国南部则相反,这一方面与春季中国云量 南多北少的分布特征以及云内液相化学反应有关,另一方面也与南北温差对气溶胶形成的影响有关。就整个中国东部而言,虽然硫酸盐的柱含量（46 Gg）仍大于硝酸盐（42 Gg）,但比较接近,反映出我国氮氧化物排放迅速增加的趋势。春季中国地区对流层中PM₁₀（空气动力学直径在10微米以下的颗粒物）及其化学成分柱含量分别为:990.8 Gg（PM₁₀）,52.6 Gg（硫酸盐）,48.2 Gg（硝酸盐）,32.1 Gg（铵盐）,22.9 Gg（黑碳）和74.1 Gg（有机碳）,有机碳（OC）中一次有机碳（POC）和二次有机碳（SOC）分别占60%和40%,中国东部PM₁₀中人为气溶胶和沙尘分别占30%和70%,反映了春季沙尘对我国大气气溶胶的重要贡献。     

Ozone Concentrations in Rural Regions of the Yangtze Delta in China

Elevated concentrations of ozone have been observed at six non-urban, surface monitoring sites in the Yangtze Delta of China during a 16-month field experiment carried out in 1999 and 2000 as part of the joint Chinese-American China-MAP Project (the Yangtze Delta of china as an Evolving Metro-Agro-Plex). The average daytime (0900–1600 h) ozone levels for the monitoring period at sites ranged from 35 to 47 ppbv (parts per billion by volume) and the mean ozone levels from 26 to 35 ppbv. Observed data show seasonal variation obviously, with highest mixing ratios of ozone in May. Average daytime ozone levels in May at sites were between 60 and 79 ppbv. High ozone concentrations were most prevalent during the late spring. Frequency counts of hourly mean ozone concentration over 60 ppbv and 40 ppbv appeared peak values of 22–39% and 42–74% in May at sites. Even higher daytime ozone levels were observed during two regional episodes, in which average daytime (0900–1600 h) ozone concentrations during 10 May and 23 May 2000 were 68 to 81 ppbv, during Oct. 18 and Oct. 28, 1999 were 59 to 67 ppbv at sites. Peak value of ozone mixing ratio appearing in late spring, instead of in summer, was attributed to summer monsoon. Backward trajectories showed that ozone episodes associated with meteorological conditions. Also many high ozone levels associated with high CO levels and high CO to NO _x ratios, which suggests a contribution from sources of emission involving incomplete combustion.     

Continuous observations of water-soluble ions in PM2.5 at Mount Tai (1534 m a.s.l.) in central-eastern China

Near real-time measurements of PM_2.5 ionic compositions were performed at the summit of the highest mountain in the central-eastern plains in the spring and summer of 2007 in order to characterize aerosol composition and its interaction with clouds. The average concentrations of total water soluble ions were 27.5 and 36.7 μg?m^?3, accounting for 44% and 62% of the PM_2.5 mass concentration in the spring and summer, respectively. A diurnal pattern of SO ₄ ^2- , NH ₄ ⁺ and NO ₃ ^- was observed in both campaigns and attributed to the upslope/downslope transport of air mass and the development of the planetary boundary layer (PBL). The average SO₂ oxidation ratio (SOR) in summer was 57% (±27%), more than twice that in spring 24% (±16%); the fine nitrate oxidation ratio (NOR) was comparable in the two seasons (9?±?6% and 11?±?10% in summer and spring, respectively). This result indicates strong summertime production of sulfate aerosol. A principal component analysis shows that short-range and long-range transport of pollution, cloud processing, and crustal source were the main factors affecting the variability of the measured ions (and other trace gases and aerosols) at Mt. Tai. Strong indications of biomass burning were observed in summer. Cloud scavenging rates showed larger variations for different ions and in different cloud events. The elevated concentrations of the water soluble ions at Mt. Tai indicate serious aerosol pollution over the North China plain of eastern China.     

Assessing the Impacts of Initial Snow Conditions over the Tibetan Plateau on China Precipitation Prediction Using a Global Climate Model

Two ensemble experiments were conducted using a general atmospheric circulation model. These experiments were used to investigate the impacts of initial snow anomalies over the Tibetan Plateau（TP） on China precipitation prediction. In one of the experiments, the initial snow conditions over the TP were climatological values; while in the other experiment, the initial snow anomalies were snow depth estimates derived from the passive microwave remote-sensing data. In the current study, the difference between these two experiments was assessed to evaluate the impact of initial snow anomalies over the TP on simulated precipitation. The results indicated that the model simulation for precipitation over eastern China had certain improvements while applying a more realistic initial snow anomaly, especially for spring precipitation over Northeast China and North China and for summer precipitation over North China and Southeast China. The results suggest that seasonal prediction could be enhanced by using more realistic initial snow conditions over TP, and microwave remote-sensing snow data could be used to initialize climate models and improve the simulation of eastern China precipitation during spring and summer. Further analyses showed that higher snow anomalies over TP cooled the surface, resulting in lower near- surface air temperature over the TP in spring and summer. The surface cooling over TP weakened the Asian summer monsoon and brought more precipitation in South China in spring and more precipitation to Southeast China during summer.     

夏季硫酸盐和黑碳气溶胶对中国云特性的影响

利用WRF-Chem（Weather Research and Forecasting model coupled with Chemistry）模式研究2006年8月1日—9月1日中国区域硫酸盐和黑碳气溶胶对云特性的影响。模式验证利用了卫星和地面观测的气象要素、化学物质浓度、气溶胶光学特性和云微物理特性。模式性能评估表明该模式能较好地抓住气象要素（温度、降水、相对湿度和风速）的量级和空间分布特征。通过与地面观测和MODIS卫星数据对比发现,尽管模式模拟还存在偏差,但还是能较好模拟出气溶胶物种的地表浓度、气溶胶光学厚度（AOD）、云光学厚度（COD）、云量（CLDF）、云顶云滴有效半径（CER）和云水路径（LWP）。通过两个敏感性试验（分别增加二氧化硫和黑碳排放量至控制试验排放的3倍）与控制试验的对比发现硫酸盐比黑碳更易成为云凝结核,在中国东部云顶云滴数浓度和其它云特性参数对二氧化硫排放增加的响应均从北向南呈递增,这与地面湿度分布有关。云滴有效半径对硫酸盐气溶胶的响应符合气溶胶第一间接效应的定义,即硫酸盐气溶胶增多,云滴数浓度增加,云滴有效半径减少,但是对黑碳气溶胶的响应在各区域不尽相同。还发现黑碳对云量的影响远大于硫酸盐,主要原因是由于黑碳气溶胶直接辐射效应（对太阳光的吸收）导致的云的“燃烧”作用。      

中国东部季风区夏季四类雨型的水汽输送特征及差异

利用1951~2015年NCEP/NCAR再分析逐日资料和中国160站月降水观测资料,及中国东部季风区夏季四类雨型（北方型、中间型、长江型和华南型）的划分结果,分析了东亚水汽输送与中国东部季风区夏季降水的关系,比较了四类雨型的水汽输送、收支特征及其差异,结果表明:（1）夏季影响中国东部季风区的水汽通道主要有以下6条:印度洋通道,表征印度季风区偏南的西风水汽输送;高原南侧通道,表征印度季风区偏北的西风水汽输送;太平洋通道,表征由西太平洋副热带高压（副高）带来的西太平洋的水汽;西风带通道,表征西风带的水汽输送;孟加拉湾通道,表征来自孟加拉湾向北的水汽输送;南海通道,表征来自印度洋和孟加拉湾在中南半岛转向及来自南海的水汽;与中国东部不同地区降水异常相联系的水汽通道存在明显的差异,且同一条水汽通道在夏季不同阶段与降水的关系也不尽相同。（2）四类雨型的水汽输送和收支特征有明显的差异,华北盛夏降水主要受亚洲季风水汽输送的影响,其次是西风带水汽输送,北方型年二者往往偏强,尤其是季风水汽输送增加一倍以上,贡献也明显增加,20世纪70年代中期之后,季风水汽输送显著减弱,西风带水汽输送的重要性相对增大;淮河流域夏季降水异常主要受太平洋通道水汽输送异常的主导,其次是高原南侧通道水汽输送,二者偏强并在淮河流域辐合时,淮河流域降水偏多形成中间型年;长江中下游地区夏季降水主要受太平洋通道水汽输送异常的主导,长江型年,副高西北侧的西南水汽输送异常加强,并与北方冷空气异常在长江中下游地区辐合,区域为正的水汽净收支;华南地区夏季降水则受印度洋通道、太平洋通道及南海通道的共同影响,当三条通道异常偏强,水汽与北方冷空气在华南地区辐合,形成华南型年。本研究所得结论加深了我们对四类雨型形成机理的认识,并为汛期主雨带的预测提供了参考。     

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。     

Climatology of Cloud-base Height from Long-term Radiosonde Measurements in China

Clouds are critical to the global radiation budget and hydrological cycle, but knowledge is still poor concerning the observed climatology of cloud-base height(CBH) in China. Based on fine-resolution sounding observations from the China Radiosonde Network(CRN), the method used to estimate CBH was modified, and uncertainty analyses indicated that the CBH is good enough. The accuracy of CBH estimation is verified by the comparison between the sounding-derived CBHs and those estimated from the micro-pulse lidar and millimeter-wave cloud radar. As such, the CBH climatology was compiled for the period 2006–16. Overall, the CBH exhibits large geographic variability across China, at both 0800 Local Standard Time(LST) and 2000 LST, irrespective of season. In addition, the summertime cloud base tends to be elevated to higher altitudes in dry regions [i.e., Inner Mongolia and the North China Plain(NCP)]. By comparison, the Tibetan Plateau(TP),Pearl River Delta(PRD) and Sichuan Basin(SCB) have relatively low CBHs( 2.4 km above ground level). In terms of seasonality, the CBH reaches its maximum in summer and minimum in winter. A low cloud base tends to occur frequently( 70%) over the TP, PRD and SCB. In contrast, at most sites over the Yangtze River Delta(YRD) and the NCP, about half the cloud belongs to the high-cloud category. The CBH does not exhibit marked diurnal variation in summer, throughout all CRN sites, probably due to the persistent cloud coverage caused by the East Asia Summer Monsson. To the best of our knowledge, this is the first CBH climatology produced from sounding measurements in China, and provides a useful reference for obtaining observational cloud base information.     

Latest update of the climatology and changes in the seasonal distribution of precipitation over China

Based on daily precipitation data from 524 meteorological stations in China during the period 1960–2009, the climatology and the temporal changes (trends, interannual, and decadal variations) in the proportion of seasonal precipitation to the total annual precipitation were analyzed on both national and regional scales. Results indicated that (1) for the whole country, the climatology in the seasonal distribution of precipitation showed that the proportion accounted for 55 % in summer (June–August), for around 20 % in both spring (March–May) and autumn (September–November), and around 5 % in winter (December–February). But the spatial features were region-dependent. The primary precipitation regime, “summer–autumn–spring–winter”, was located in central and eastern regions which were north of the Huaihe River, in eastern Tibet, and in western Southwest China. The secondary regime, “summer–spring–autumn–winter”, appeared in the regions south of the Huaihe River, except Jiangnan where spring precipitation dominated, and the southeastern Hainan Island where autumn precipitation prevailed. (2) For the temporal changes on the national scale, first, where the trends were concerned, the proportion of winter precipitation showed a significantly increasing trend, while that of the other three seasons did not show any significant trends. Second, for the interannual variation, the variability in summer was the largest among the four seasons and that in winter was the smallest. Then, on the decadal scale, China experienced a sharp decrease only in the proportion of summer precipitation in 2000. (3) For the temporal changes on the regional scale, all the concerned 11 geographic regions of China underwent increasing trends in the proportion of winter precipitation. For spring, it decreased over the regions south of the Yellow River but increased elsewhere. The trend in the proportion of summer precipitation was generally opposite to that of spring. For autumn, it decreased over the other ten regions except Inner Mongolia with no trend. It is noted that the interannual variability of precipitation seasonality is large over North China, Huanghuai, and Jianghuai; its decadal variability is large over the other regions, especially over those regions south of the Yangtze River.     

中国降水的季节性

本文使用一套基于中国气象局所属的2416个台站数据所得的高分辨降水资料,对1961~2013年中国降水季节性进行了研究。就全国平均而言,各季节降水占全年降水百分率最高的为夏季（56.5%）,春季（19.3%）和秋季（18.9%）次之,冬季（5.3%）最少;针对不同地区,各季节降水百分率存在很大差异,例如华南春季降水最多、东北至高原一线秋季降水大于春季降水。春、夏两季降水百分率高值（低值）区域略呈现出降水百分率减少（增多）趋势,秋季整体上略微减少,冬季则显著增加;季节降水百分率的变率整体表现为夏季大而冬季小,其西部的变率与地形为显著负相关,东部变率的大值区位置随季节变化;秋冬两季的降水百分率变率有显著增加,各季节不同地区变率的变化趋势存在明显差异。     

THE RADIATIVE EFFECTS OF ANTHROPOGENIC AEROSOLS OVER CHINA AND THEIR SENSITIVITY TO SOURCE EMISSION

In this paper,the RIEMS 2.0 model,source emission in 2006 and 2010 are used to simulate the distributions and radiative effects of different anthropogenic aerosols over China.The comparison between the results forced by source emissions in 2006 and 2010 also reveals the sensitivity of the radiative effects to source emission.The results are shown as follows:(1) Compared with those in 2006,the annual average surface concentration of sulfate in 2010 decreased over central and eastern China with a range of-5 to 0 μg/m~3;the decrease of annual average aerosol optical depth of sulfate over East China varied from 0.04 to 0.08;the annual average surface concentrations of BC,OC and nitrate increased over central and eastern China with maximums of 10.90,11.52 and 12.50μg/m~3,respectively;the annual aerosol optical depths of BC,OC and nitrate increased over some areas of East China with extremes of 0.006,0.007 and 0.008,respectively.(2)For the regional average results in 2010,the radiative forcings of sulfate,BC,OC,nitrate and their total net radiative forcing at the top of the atmosphere over central and eastern China were-0.64,0.29,-0.41,-0.33 and-1.1 W/m~2,respectively.Compared with those in 2006,the radiative forcings of BC and OC in 2010 were both enhanced,while that of sulfate and the net radiative forcing were both weakened over East China mostly.(3)The reduction of the cooling effect of sulfate in 2010 produced a warmer surface air temperature over central and eastern China;the maximum value was 0.25 K.The cooling effect of nitrate was also slightly weakened.The warming effect of BC was enhanced over most of the areas in China,while the cooling effect of OC was enhanced over the similar area,particularly the area between Yangtze and Huanghe Rivers.The net radiative effect of the four anthropogenic aerosols generated the annual average reduction and the maximum reduction were-0.096 and-0.285 K,respectively,for the surface temperature in 2006,while in 2010 they were-0.063 and-0.256 K,respectively.In summary,the change in source emission lowered the cooling effect of anthropogenic aerosols,mainly because of the enhanced warming effect of BC and weakened cooling effect of scattering aerosols.