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1.
Long-term measurements of fine particle number-size distributions were carried out over 9.5 yr (May 1997–December 2006), in the urban background atmosphere of Helsinki. The total number of days was 3528 with about 91.9% valid data. A new particle formation event (NPF) is defined if a distinct nucleation mode of aerosol particles is observed below 25 nm for several hours, and it shows a growth pattern. We observed 185 NPF events, 111 d were clear non-events and most of the days (around 83.5%) were undefined. The observed events were regional because they were observed at Hyytiälä (250 km north of Helsinki). The events occurred most frequently during spring and autumn. The observed formation rate was maximum during the spring and summer (monthly median 2.87 cm−3 s−1) and the modal growth rate was maximum during late summer and Autumn (monthly median 6.55 nm h−1). The events were observed around noon, and the growth pattern often continued on the following day. The observation of weak NPF events was hindered due to pre-existing particles from both local sources. It is clear that regional NPF events have a clear influence on the dynamic behaviour of aerosol particles in the urban atmosphere.  相似文献   

2.
西北地区气溶胶光学特性及辐射影响   总被引:3,自引:1,他引:2  
利用SACOL(兰州大学半干旱气候与环境观测站)2006~2012年AERONET(全球气溶胶自动监测网)level 2.0和太阳短波辐射计资料,分析了中国西北地区气溶胶的光学特性与辐射影响。利用辐射传输模式SBDART(平面平行大气辐射传输模式)检验TOA(大气层顶)处辐射强迫为正的原因。BOA(地表)、TOA、Atmosphere(大气)的辐射强迫年均值分别是-59.43 W m-2、-17.03 W m-2、42.40 W m-2,AOD(光学厚度,550 nm)年均值0.37,α(波段的波长指数,440~675 nm)年均值0.91,变化趋势与AOD位相相反,当AOD为0.3~2.2时,α很小(0.0~0.2),表明粒子尺度很大。SSA(单次散射反照率,675 nm)年均值0.93,g(不对称因子,675 nm)年均值0.68,复折射指数(675 nm)实部年均值1.48,虚部0.007。复折射指数实部的年变化趋势与AOD一致,虚部与AOD反位相,所以西北地区多为粗模态散射性气溶胶。气溶胶对大气的加热率最大值出现在0~2 km,随高度递减。冬、夏半年在地表加热率分别是2.6 K d-1和0.6 K d-1;季节变化中,冬季、秋季、春季和夏季,在地表的加热率依次是2.5 K d-1、1.4 K d-1、1.2 K d-1和0.2 K d-1,主要因为秋季气溶胶的吸收性大于春季。地表反照率和SSA对TOA正辐射强迫贡献率分别是22.5%和77.5%。  相似文献   

3.
Particle number size distribution(PNSD) between 10 nm and 20 μm were measured in the Pearl River Delta(PRD) region in winter 2011.The average particle number concentration of the nucleation mode(10-20 nm),Aitken mode(20-100 nm),accumulation mode(100 nm-1μm) and coarse mode(1-20 μm) particles were 1 552,7 470,4 012,and 19 cm-3,respectively.The volume concentration of accumulation mode particles with peak at 300 nm accounted for over 70% of the total volume concentration.Diurnal variations and dependencies on meteorological parameters of PNSD were investigated.The diurnal variation of nucleation mode particles was mainly influenced by new particle formation events,while the diurnal variation of Aitken mode particles correlated to the traffic emission and the growth process of nucleation mode particles.When the PRD region was controlled by a cold high pressure,conditions of low relative humidity,high wind speed and strong radiation are favorable for the occurrence of new particle formation(NPF) events.The frequency of occurrence of NPF events was 21.3% during the whole measurement period.Parameters describing NPF events,including growth rate(GR) and source rate of condensable vapor(Q),were slightly larger than those in previous literature.This suggests that intense photochemical and biological activities may be the source of condensable vapor for particle growth,even during winter in the PRD.  相似文献   

4.
利用2014年7月黄山光明顶观测获得的气溶胶数浓度、气溶胶数谱数据,对黄山夏季气溶胶数浓度及谱分布特征进行分析,并在此基础上对气溶胶数谱进行了对数正态分布拟合。研究结果表明:黄山夏季气溶胶平均数浓度约为3 518.27 cm~(-3),主要集中在爱根核模态;气溶胶平均数浓度日变化呈双峰分布,峰值浓度的出现伴随着小粒子的增多。气溶胶数浓度与相对湿度和风速成负相关,高浓度的气溶胶多出现在较弱的东南风时;积聚模态气溶胶数浓度受风向影响显著。不同气团背景下气溶胶数谱差异集中在小于100 nm和500~1 000 nm粒径范围。爱根核模态气溶胶在高湿的西南气团影响下数浓度最低、谱较窄,而高温、低湿的东南气团对应的气溶胶数浓度最高、谱最宽,北方气团对应的气溶胶数浓度和谱宽居中;500~1 000 nm粒径范围气溶胶数谱分布特征与之相反。不同背景的气溶胶数谱和体积谱均可采用爱根模态、积聚模态1和积聚模态2三个模态进行对数正态分布拟合,但不同气团背景下的各模态谱型参数差异较大。  相似文献   

5.
通过实验收集大气颗粒物,对南京地区大气气溶胶谱分布进行了描述,对气溶胶分布与相对湿度的相关性进行了探讨。建立了南京地区7—11月气溶胶化学组分的月平均模型,得出气溶胶等效复折射率的预测方法。结果表明:南京地区的大气气溶胶颗粒物,峰值粒径在80~100 nm范围,属于典型的城市型气溶胶。数浓度与相对湿度的相关性与季节和粒径大小有关,在6—9月,相对湿度与细粒子数浓度呈负相关,与粗粒子呈正相关,在10—11月相反,且易受极端天气影响。建立的干气溶胶等效复折射率月平均模型,结合湿度修正模型得到某一日的复折射率,与AERONET站点数据进行了对比,结果较为一致,误差范围在0~0.03。  相似文献   

6.
基于2016年冬季和2017年夏季在北京、2016年夏季在邢台的三次气溶胶外场观测实验,选取三次观测期间典型的新粒子生成事件,分析其对气溶胶吸湿和云凝结核(CCN)活化特性的影响。两地分别位于华北平原北部超大城市区域和中南部工业化区域,两地不同季节新粒子形成机制不同,对应的凝结汇、生长速率以及气溶胶化学组分也不同。北京站点新粒子生成事件的发生以有机物的生成主导,而邢台站点新粒子生成事件的发生则以硫酸盐和有机物的生成共同主导。邢台站点新粒子生成过程中气溶胶吸湿性及云凝结核活化能力明显强于北京站点,此特点在核模态尺度粒子中表现尤为明显。以上结果表明,在估算新粒子生成对CCN数浓度的影响时,应充分考虑气溶胶吸湿和活化特性的差异。  相似文献   

7.
感应电机矢量控制系统的仿真研究   总被引:6,自引:0,他引:6  
根据2008年4—7月黄山大气气溶胶观测资料,研究了气溶胶粒子的数浓度、谱分布特征及其与气象因子的关系,探讨了雾天和非雾天气溶胶颗粒物时间和尺度分布特点。分析发现,黄山光明顶春、夏季大气气溶胶数浓度的平均值分别为3.14×103个/cm3和1.80×103个/cm3,其中超细粒子(粒径小于0.1μm的粒子)在春夏季分别约占总粒子数浓度的79%和68%;高数浓度值集中在粒径0.04~0.12μm;积聚模态气溶胶粒子(0.1~1.0μm)在体积浓度分布和表面积分布中占很大比例。结合气象资料比较了雾天与非雾天气溶胶分布的差异,发现细粒子浓度非雾天大于雾天,而气溶胶数浓度与温度呈正相关,与相对湿度成反相关。结果还发现,黄山在春季以西北风和偏南风为主,西北风时气溶胶数浓度较高,在夏季主要以偏南风,特别是西南风为主,但是气溶胶数浓度的高值多发生在偏东风的条件下。  相似文献   

8.
In order to understand the seasonal variation of aerosol optical properties in the Yangtze River Delta,5 years of measurements were conducted during September 2005 to December 2009 at Taihu,China.The monthly averages of aerosol optical depth were commonly >0.6;the maximum seasonal average(0.93) occurred in summer.The magnitude of the Angstr¨om exponent was found to be high throughout the year;the highest values occurred in autumn(1.33) and were the lowest in spring(1.08).The fine modes of volume size distribution showed the maxima(peaks) at a radius of ~0.15 μm in spring,autumn,and winter;at a radius of ~0.22 μm in summer.The coarse modes showed the maxima(peaks) at a radius of 2.9 μm in spring,summer,and autumn and at a radius of 3.8 μm in winter.The averages of single-scattering albedo were 0.92(spring),0.92(summer),0.91(autumn),and 0.88(winter).The averages of asymmetry factor were found to be larger in summer than during other seasons;they were taken as 0.66 at 440-1020 nm over Taihu.The real part of the refractive index showed a weak seasonal variation,with averages of 1.48(spring),1.43(summer),1.45(autumn),and 1.48(winter).The imaginary parts of the refractive index were higher in winter(0.013) than in spring(0.0076),summer(0.0092),and autumn(0.0091),indicating that the atmosphere in the winter had higher absorbtivity.  相似文献   

9.
南京霾天颗粒物数浓度特征及其受气象条件影响分析   总被引:5,自引:3,他引:2  
2013年12月,我国中东部地区爆发持续性霾污染过程。本研究利用空气动力学粒径谱仪和气溶胶粒径谱仪在线观测这次霾污染过程中13.6~20 000 nm颗粒物数浓度,结合气象参数和颗粒物化学组分对南京霾天颗粒物数浓度分布特征,及其与气象条件相关性进行分析。结果表明,霾天颗粒物主要分布在积聚模态,且500~1 000 nm和1 000~2 500 nm粒径段颗粒物数浓度的增多是造成霾天能见度低的主要原因;随着相对湿度的增大,13.6~100 nm粒径段颗粒物数浓度逐渐降低,而大于100 nm颗粒物数浓度升高;500~1 000 nm和1 000~2 500 nm粒径段颗粒物数浓度受相对湿度的影响尤为明显,并且这2个粒径段颗粒物受气态污染物(SO2,NOX)的二次转化影响较大。霾污染期间南京大气颗粒物主要来自南京东南和西北方向的污染源排放,颗粒物数浓度总体上与风速呈负相关关系;温度对颗粒物数浓度的影响主要集中在13.6~100 nm粒径段;边界层的高度与粒径100 nm颗粒物呈负相关性,边界层的抬升反而利于超细粒子的生成和增长;逆温层的强度对超细粒子的作用更为明显。  相似文献   

10.
By analyzing airborne observations over North China from 30 flights during spring and autumn of 2005-2007, characteristics of the vertical distributions of aerosol and cloud condensation nuclei (CCN) at 0.3% supersaturation in various locations of North China are investigated. The measurement samplings were conducted over different surfaces such as plains, plateau, and sea. The results show that the number concentration of accumulation mode aerosols was greater in autumn than in spring, but the reverse is true for CCN. This means that more aerosols with diameters smaller than 100 nm could be activated as CCN in spring, and this could induce higher aerosol activation efficiency. The aerosol activation efficiency over the plains near the Taihang Mountain was greater in spring than in autumn, and it was greater over sea than over land. The aerosol activation efficiency above the boundary layer over the Bashang Plateau was very low. Based on a fit of the negative exponential vertical distributions of aerosol and CCN, a spatial parameterization model of aerosol and CCN as well as aerosol activation efficiency over North China was proposed. The results show that aerosol activation efficiency was not clearly dependent on altitude because it was mainly affected by regional physical and chemical characteristics of aerosols and the ambient atmospheric conditions. The mean aerosol activation efficiency is 0.66, with values of 0.70 and 0.53 in spring and autumn,respectively.  相似文献   

11.
南京不同天气和能见度下云凝结核的观测分析   总被引:3,自引:1,他引:2  
王惠  刘晓莉  安俊琳  丁伟 《气象科学》2016,36(6):800-809
利用美国DMT公司生产的云凝结核(Cloud Condensation Nuclei,CCN)计数器(DMTCCNC),对2013年4—12月南京地区CCN进行观测。对不同天气条件下CCN活化谱拟合,霾天C值最高,为13 085 cm-3,雨后C值降至8 054 cm-3,属于大陆性核谱。不同能见度条件下CCN活化谱特征有明显差异,南京地区不同程度霾天CCN数浓度均远高于轻雾天,浓雾时期CCN数浓度显著偏高。CCN数浓度受到气象要素和天气状况、气溶胶源排放等因素影响。南京地区气溶胶凝结核(Condensation Nuclei,CN)数浓度和CCN数浓度的拟合结果显示出较好的相关性。CCN数浓度值:冬季春季秋季夏季,春季CCN数浓度日变化有三峰趋势,夏季基本呈单峰型,秋季、冬季双峰特征突出。气溶胶源排放、环境气象条件和气溶胶理化特性均会影响CCN数浓度的季节变化。  相似文献   

12.
Fine particle of organic aerosol(OA), mostly arising from pollution, are abundant in Beijing. To achieve a better understanding of the difference in OA in summer and autumn, a high-resolution time-of-flight aerosol mass spectrometer(HRTo F-AMS, Aerodyne Research Inc., USA) was deployed in urban Beijing in August and October 2012. The mean OA mass concentration in autumn was 30 ± 30 μg m-3, which was higher than in summer(13 ± 6.9 μg m-3). The elemental analysis found that OA was more aged in summer(oxygen-to-carbon(O/C) ratios were 0.41 and 0.32 for summer and autumn,respectively). Positive matrix factorization(PMF) analysis identified three and five components in summer and autumn, respectively. In summer, an oxygenated OA(OOA), a cooking-emission-related OA(COA), and a hydrocarbon-like OA(HOA)were indentified. Meanwhile, the OOA was separated into LV-OOA(low-volatility OOA) and SV-OOA(semi-volatile OOA);and in autumn, a nitrogen-containing OA(NOA) was also found. The SOA(secondary OA) was always the most important OA component, accounting for 55% of the OA in the two seasons. Back trajectory clustering analysis found that the origin of the air masses was more complex in summer. Southerly air masses in both seasons were associated with the highest OA loading, while northerly air masses were associated with the lowest OA loading. A preliminary study of OA components,especially the POA(primary OA), in different periods found that the HOA and COA all decreased during the National Day holiday period, and HOA decreased at weekends compared with weekdays.  相似文献   

13.
2010年长江三角洲临安本底站PM2.5理化特征   总被引:2,自引:0,他引:2       下载免费PDF全文
2010年在代表长三角区域背景地区的浙江省临安区域大气本底站开展了对大气细粒子PM2.5为期1年的地面观测,并对细粒子中水溶性离子和碳组分的季节变化特征进行了分析。临安2010年大气中PM2.5质量浓度平均为 (58.2±50.8) μg·m-3,PM2.5质量浓度季节变化明显。利用HYSPLIT4模式计算了2010年临安72 h后向轨迹,根据轨迹计算与聚类结果,结合地面观测的PM2.5数据进行了分析。研究表明:临安地区因受到长江三角洲区域及偏北气流引起的污染传输影响,呈现出高细粒子水平特征。PM2.5中总水溶性离子年平均质量浓度为 (28.5±17.7) μg·m-3,占PM2.5质量浓度的47%。其中,气溶胶组分SO42-,NO3-和NH4+所占比例最大,共占总水溶性离子的69%。PM2.5中有机碳和元素碳的年平均质量浓度分别为 (10.1±6.7) μg·m-3和 (2.4±1.8) μg·m-3。有机碳和元素碳质量浓度显著相关,表明有机碳和元素碳主要来自相同的排放源。  相似文献   

14.
南京北郊冬季大气气溶胶及其湿清除特征研究   总被引:18,自引:0,他引:18  
利用WPS(宽范围颗粒粒径谱仪)、雨滴潜仪和雾滴谱仪测量了2007~2008年冬季南京北郊大气气溶胶数浓度谱分布和降水强度,分析了气溶胶粒子的分布特征以及气溶胶粒径与湿清除系数的关系.结果表明:气溶胶粒子具有明显的双峰型R变化特征,数浓度主要集中在0.02~O.2μm粒径范围内,受汽车尾气排放、混合层高度变化以及颗粒物水平输送的影响较大.降雨、降雪和雾过程都对气溶胶粒子有不同程度的清除,降雨和浓雾对核模态和粗模态的气溶胶粒子的清除能力显著,降雪对粒径小于0.03μm的气溶胶粒子的清除能力较强.  相似文献   

15.
塔克拉玛干沙漠地区气溶胶光学厚度卫星遥感产品验证   总被引:2,自引:0,他引:2  
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。  相似文献   

16.
北京PM1中的化学组成及其控制对策思考   总被引:5,自引:0,他引:5       下载免费PDF全文
通过分析北京城区2007年夏季和秋季、2008年冬季和春季4个季节PM1中硫酸盐、硝酸盐、铵盐、有机物和黑碳等气溶胶化学组成,结合对我国及全球主要区域PM10中上述气溶胶组分及矿物气溶胶组成的评估,发现因受干旱区产生的沙尘和城市逸散性粉尘的共同影响,整个亚洲大陆,尤其是我国的矿物气溶胶浓度与欧美国家城市区域气溶胶总和的平均值相当或更高。我国在重视控制PM2.5等细粒子污染的同时,不应忽视对PM2.5~PM10之间粗粒子的控制力度;北京城区春、夏、秋、冬的PM1平均质量浓度分别约为94,74,66 μg·m-3和91 μg·m-3,全年平均约为81 μg·m-3,其中有机物气溶胶约占41%,硫酸盐占16%,硝酸盐占13%,铵盐占8%,黑碳和氯化物分别占11%和3%,细矿物气溶胶约贡献7%。对于PM2.5污染的控制,关键是消减PM1中主要气溶胶粒子的排放与转化,其中对有机物的控制更为重要,尽管对于北京而言进一步污染控制的难度已经很大。从科学上来说,即使我国的控制措施能百分之百实现,也很难稳定地达到欧美国家的空气质量水平,因为我国本底矿物气溶胶的浓度较高。应进一步评估各项控制措施的适用性,并制定考虑我国人群健康状况的PM2.5空气质量标准。  相似文献   

17.
利用1960—2005年京津冀地区的地面太阳辐射资料,综合分析了该地区45年太阳辐射的分布状况和变化趋势,并结合云量、降水量、气溶胶光学厚度和大气含水量,分析了该地区太阳辐射的变化原因。结果表明:(1)京津冀地区的太阳辐射并没有出现20世纪80年代末到90年代中期的"变亮"现象;同期冬、春季总辐射下降,夏、秋季上升;(2)在1985—1997年间,依据总辐射变化情况,京津冀地区被分为截然相反的两个区域:东部地区总辐射增加,倾向率为1.016 MJ.m-2.mon-1.(10a)-1;西部地区总辐射减少,倾向率为10.092MJ.m-2.mon-1.(10a)-1;(3)总辐射增加的区域,主要是由于云量减少、降水量减少所伴随的日照时数增加以及气溶胶光学厚度降低所造成的;(4)总辐射减少的区域,云量、气溶胶光学厚度和降水量变化并不显著,总辐射持续减少。  相似文献   

18.
Under cloudy conditions at the Gosan Climate Observatory (GCO), Korea, we observed distinct new particle formation and growth (NPF) events from simultaneous co-located measurements of aerosol and cloud profiles, cloud cover, shortwave radiation, and the number concentration and size distribution of aerosols. The high frequency of NPF was observed at GCO under decreased downwelling solar radiation caused by clouds. Although we observed about 15 and 40 % decreases in downwelling surface shortwave radiations, in the presence of thick mid-level (low-level) clouds, on January 28 and 30, 2012, respectively, distinct NPFs with a growth rate of 3.3 (3.9) nm h?1 were observed. We examined a 4-year series (May 2008 to April 2012) of continuous measurements of the size distribution of aerosol numbers and visually observed cloud cover. We found that approximately 13 % (i.e., 35 days out of 280 days) of total NPF events were observed under cloud-free conditions (i.e., cloud cover of 0/10). About 20 % (i.e., 57 days out of 280 days) of total NPF events occurred under mostly overcast conditions (i.e., cloud cover of 9/10–10/10). Although NPF events occurring under cloudy conditions were also found elsewhere, the frequency of NPF occurring at GCO seems much higher. The average value of relative humidity for the strong-NPF event days is lower than that of the weak and non-NPF event days for all cloud categories. No significant difference in the condensation sink was found among strong-, weak-, and non-NPF days, but the condensation sink showed a slight decreasing tendency with increasing cloudiness. Further investigations on precursor gases and preexisting aerosols under cloudy conditions are needed.  相似文献   

19.
Measurements were performed in spring 2001 and 2002 to determine the characteristics of soil dust in the Chinese desert region of Dunhuang, one of the ground sites of the Asia-Pacific Regional Aerosol Characterization Experiment (ACE-Asia). The mean mass concentrations of total suspended particle matter during the spring of 2001 and 2002 were 317 μg m-3 and 307 μg m-3, respectively. Eleven dust storm events were observed with a mean aerosol concentration of 1095 μg m-3, while the non-dusty days with calm or weak wind speed had a background aerosol loading of 196 μg m-3 on average in the springtime.The main minerals detected in the aerosol samples by X-ray diffraction were illite, kaolinite, chlorite, quartz,feldspar, calcite and dolomite. Gypsum, halite and amphibole were also detected in a few samples. The mineralogical data also show that Asian dust is characterized by a kaolinite to chlorite (K/C) ratio lower than 1 whereas Saharan dust exhibits a K/C ratio larger than 2. Air mass back-trajectory analysis show that three families of pathways are associated with the aerosol particle transport to Dunhuang, but these have similar K/C ratios, which further demonstrates that the mineralogical characteristics of Asian dust are different from African dust.  相似文献   

20.
利用3个架次的积分浊度仪和PCASP-100X(Passive Cavity Aerosol Spectrometer Probe)机载观测资料,分析了2013年山西夏季空中有云、无云和少云3种不同条件下气溶胶散射系数的分布特征,讨论了气溶胶散射系数垂直变化与气溶胶数浓度、气象条件的关系,并结合HYSPLIT(Hybrid of Single Particle Lagrangian Integrated Trajectory model)后向轨迹模型研究气溶胶的运动轨迹和可能的污染来源。结果表明:山西夏季空中气溶胶总散射系数变化范围为0~499 Mm-1,晴空气溶胶数浓度和总散射系数明显大于有云和少云时。气溶胶总散射系数一般随高度的增加而递减。造成气溶胶总散射系数、数浓度偏高的原因有下垫面污染源多、风速小、相对湿度高以及逆温层的存在。550 nm波段气溶胶后向散射比大于0.1,粒径0.1~0.5 μm的气溶胶粒子对散射影响最大,说明山西空中细粒子污染比较严重。气溶胶总散射系数与数浓度有一定的相关性。引起气溶胶总散射系数、数浓度较高的气团传输路径主要为西南路径,局地排放的气溶胶大于远距离传输的气溶胶对散射系数的贡献。  相似文献   

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