Study on the Characteristics of Atmospheric Dry and Wet Deposition in the Upper Reaches of Baiyangdian

To study the characteristics of atmospheric dry and wet deposition in the upper reaches of Baiyangdian,two sampling sites in Baoding City were monitored for 1 year from September 2018 to August 2019.The results showed that the dry and wet deposition fluxes of total nitrogen(TN)during the monitoring period were 6.87 and 6.46 kg/(hm^(2)·a),respectively.The ratio of wet to dry deposition of TN was approximately 1∶1,with wet deposition being dominated by ammonium nitrogen deposition.The dry and wet deposition fluxes of total phosphorus(TP)were 0.228 and 0.125 kg/(hm^(2)·a),and it was dominated by dry deposition.The average concentration of TN in wet deposition exceeded the standard threshold for eutrophic waters,and its ecological effects on the Baiyangdian basin should be concerned.Wet deposition fluxes of nitrogen and phosphorus had a significantly positive correlation with rainfall,while their deposition concentrations were negatively correlated with rainfall.The dry deposition of atmospheric nitrogen and phosphorus was influenced by the amount of dustfall and climatic factors such as rainfall,temperature,and humidity,which mainly occurred from April to August.

Annual Fluxes of Heavy Metal Elements in Atmospheric Dry and Wet Depositions in the Pearl River Delta Economic Region, Guangdong Province

There are 158 sampling points to be set up in the Pearl River delta economic region. The collecting period is mostly one year, namely, from July 2007 to July 2008. The eight heavy metal elements of Cr, Ni, Cu, Pb, Zn, As, Hg, and Cd in 474 dry and wet deposition samples were tested in terms of the standard procedures. Their average annual fluxes have no obvious difference between dry deposition and wet deposition. So these elements might be at an equilibrium or quasi-equilibrium state between dry deposition and wet deposition.

Major Ions in Atmospheric Deposition in Lake Kivu Basin

This study investigated the major ion composition and sources in wet and dry deposition samples collected over 15 months (December 2017 to February 2019) at four stations representing four different land use/cover types on the western side of Lake Kivu basin in D.R. Congo. The samples were collected every 13 days for dry deposition and two to three times per month for wet deposition. Samples were analyzed for major ionic components (Cl-, NO-3, SO2-4, Na+, K+, NH+4, Ca2+, CO2-3, HCO-3 and Mg2+). Electrical conductivity and pH were analyzed immediately in the field while major ion measurements were in the laboratory. Results showed the pH of both the dry and the wet depositions were higher than what would have been expected based on equilibration with atmospheric CO2 (pH > 5.6) at all four sites, with conductivity less than 50 μS/cm. The neutralization process in dry and wet atmospheric deposition is due to Ca2+, NH+4, HCO-3 and CO2-3. The anion: cation ratio in dry deposition was close to 1 for Iko and Bukavu, and it was greater than 1.0 (1.1 - 1.2) for Lwiro and Goma in wet deposition. The dominant anions in wet deposition were SO2-4 and NO-3, found around the rural area near cement factory and the urban area near active volcanoes, respectively. The most abundant cation was Na+ followed by K+. The enrichment factors and correlation analysis suggest that the main sources of Ca2+, Na+ and Mg2+ were disintegration of soil processes, aeolian suspension of soil and volcanic ash, biomass burning and the cement/lime factory around the Lake Kivu basin.

Wet and dry deposition fluxes of heavy metals in Pearl River Delta Region(China):Characteristics,ecological risk assessment,and source apportionment

The atmospheric deposition of heavy metals poses serious risks to the ecological system and human health. To advance our knowledge of atmospheric dry/wet heavy metal deposition in the PRD region, monthly fluxes were examined based on soluble/insoluble fractions of five heavy metal elements（Cu, Pb, Cd, Cr and Zn） in samples collected from January 2014 to December 2015 at Guangzhou（urban） and Dinghushan（suburban） sites. The ratios of wet/dry deposition fluxes indicated that heavy metal deposition was governed by wet deposition rather than dry deposition in the PRD region. Affected by the shifting of the Asian monsoon, wet deposition fluxes exhibited significant seasonal variation between summer monsoon seasons（April to September） and winter monsoon seasons（October to February） in this region. Cd was classified as an extremely strong potential ecological risk based on solubility and the Hakanson ecological risk index. Source contributions to wet deposition were calculated by PMF, suggesting that dust, biomass burning, industries,vehicles, long-range transport and marine aerosol sources in Guangzhou, and Zn fertilizers,marine aerosol sources, agriculture, incense burning, biomass burning, vehicles and the ceramics industry in Dinghushan, were the potential sources of heavy metals.

Atmospheric wet and dry deposition of dissolved inorganic nitrogen to the South China Sea

At the global scale,atmospheric inputs of nitrogen are an important source of the new nitrogen that supports new marine production,especially in oligotrophic open oceans and marginal seas.This study reports quantities of atmospheric deposition of dissolved inorganic nitrogen(DIN)to the largest marginal sea in the North Pacific(the oligotrophic South China Sea,SCS)based primarily on rainwater sampling in the open northwestern region(Yongxing Island)from 2013 to 2015,and aerosol sampling from the SCS basin in June 2017.Atmospheric wet and dry deposition of DIN and their potential contributions to productivity were estimated.The volume-weighted mean rainwater concentrations during the wet and dry seasons were 4.9 and 18.1μmol L-1 for N+N(NO3-+NO2-),and 5.7 and 4.0μmol L-1 for NH4+,respectively.Rainwater concentrations of DIN were lower in the marginal seas than in the open ocean.The aerosol NO3-concentration was 1.15±1.18μg m-3 during the wet season,which is slightly lower than reported for the East China Sea and East Sea,but higher than in the Arabian Sea.Monthly wet and dry deposition rates ranged from 0.4-3.9 and 0.4-1.2 mmol m-2 mon-1 for NO3-,and 0.2-1.3 and 0.01-0.02 mmol m-2 mon-1 for NH4+,respectively.The annual wet and dry deposition fluxes of DIN were estimated to be 16.8 and 10.1 mmol m-2yr-1,respectively.Compared to other marginal seas,the SCS receives less atmospheric NO3-inputs than the Yellow Sea,East China Sea,East Sea,and northeastern Mediterranean Sea.The total atmospheric DIN deposition may account for 1.8-11.1%of the nitrogen supporting new production and 0.7-1.8%of the nitrogen supporting primary production.

The study on the depositional styles of major ions and the climatic effect of nssSO_4^(2-)in Princess Elizabeth Land, Antarctica

Snow samples collected from a 50 m firn core and two snow pits along the route of the 1996/1997 Chinese First Antarctic Inland Traverse Expedition in Princess Elizabeth Land, East Antarctica, have been analyzed for chemical composition and oxygen isotope ratio. Analyzing the relationship between the concentration and flux of major ions and accumulation rate can draw the following conclusions. 1) The concentrations of major ions in the atmosphere in the study region is big enough so that the concentrations of the ions do not vary with snow accumulation rate, that is to say, the concentrations of major chemical species are independent of snow accumulation rate. 2) The results of analyzing the depositional styles of major chemical species suggest that wet deposition dominates the major ions flux. In addition, there is no apparent correlation between nssSO 2- 4 fluctuations and isotope profile. This would indicate the short-term climatic effect of volcanism is not evident in the region.

NUMERICAL MODELING OF AIR POLLUTANT AND RAINFALL EFFECT ON ACID WET DEPOSITION

It is helpful to go deep into understanding the acid rainfall through studying the relation of two centers between acid deposition and rainfall and the relation of intensity between them.We adopt a three-dimensional Eulerian regional acid deposition model,or NCAR-RADM,to calculate regional chemical concentrations and dry and wet depositions of acids.The temporally and spatially varied meteorological field is provided by a mesoscale meteorological model,vertion 4.We calculate dry and wet depositions of acids in eight kinds of different rainfall distributions.The results show that the wet depositions of acids near pollutant source is very sensitive to rainfall intensity in initial stage.The distribution of acid wet deposition will tend to that of rainfall intensity when rainfall intensity is small in source.And it will tend to that of initial pollutant concentration when rainfall intensity is large in source.

Atmospheric deposition of inorganic nitrogen in a semi-arid grassland of Inner Mongolia, China

Due to increasing global demand for crop production and energy use, more and more reactive nitrogen（Nr） has been generated and emitted to the environment. As a result, global atmospheric nitrogen（N） deposition has tripled since the industrial revolution and the ecological environment and human health have been harmed. In this study, we measured dry and wet/bulk N deposition from July 2013 to December 2015 in a semi-arid grassland of Duolun County, Inner Mongolia, China. The samples of dry and wet/bulk N deposition were collected monthly with a DELTA（DEnuder for Long Term Atmospheric sampling） system and with Gradko passive samplers and a precipitation gauge. The measured results show that the annual mean concentrations of NH_3, NO_2, HNO_3, particulate NH_4~＋（pNH_4~＋） and particulate NO_3^-（pNO_3^-） in atmosphere were 2.33, 1.90, 0.18, 1.42 and 0.42 μg N/m3, respectively, and that the annual mean volume-weighted concentrations of NH_4~＋-N and NO_3^--N in precipitation were 2.71 and 1.99 mg N/L, respectively. The concentrations of Nr components（including NH_3, NO_2, HNO_3, p NH_4~＋, pNO_3^-, NH_4~＋-N and NO_3^--N） exhibited different seasonal variations. Specifically, NO_2 and HNO_3 exhibited higher concentrations in autumn than in summer, while the other Nr components（NH_3, pNH_4~＋, pNO_3^-, NH_4~＋-N and NO_3^--N） showed the highest values in summer. Based on measured concentrations of Nr components and their deposition velocities estimated using the GEOS-Chem global atmospheric chemical transport model, the calculated annual mean dry deposition fluxes were 3.17, 1.13, 0.63, 0.91 and 0.36 kg N/（hm^2·a） for NH_3, NO_2, HNO_3, p NH_4~＋ and pNO_3^-, respectively, and the calculated annual mean wet/bulk deposition fluxes were 5.37 and 3.15 kg N/（hm^2·a） for NH_4~＋-N and NO_3^--N, respectively. The estimated annual N deposition（including dry N deposition and wet/bulk N deposition） reached 14.7 kg N/（hm^2·a） in grassland of Duolun County, approaching to the upper limit of the N critical load（10–15 kg N/（hm^2·a））. Dry and wet/bulk deposition fluxes of all Nr components（with an exception of HNO_3） showed similar seasonal variations with the maximum deposition flux in summer and the minimum in winter. Reduced Nr components（e.g., gaseous NH_3 and p NH_4~＋ in atmosphere and NH_4~＋-N in precipitation） dominated the total N deposition at the sampling site（accounted for 64% of the total N deposition）, suggesting that the deposited atmospheric Nr mainly originated from agricultural activities. Considering the projected future increases in crop and livestock production in Inner Mongolia, the ecological and human risks to the negative effects of increased N deposition could be increased if no mitigation measures are taken.

Relationship between Nitrogen Atmospheric Deposition, Discharge and Concentration, and Monthly Change of Those in a River

The hypothesis that the product of discharge and concentration of nitrogen (N) in river water is equal to the atmospheric deposition was verified in the mountainous basin of the Tedori River in Japan. To verify this relationship, long-term data?are required to eliminate the effect of short-term variation of the N components. The basin has very high mountains, including Mount Hakusan (2702 maltitude), which is covered with deep snow in winter. Therefore, limited data were used for the estimation of the deposition of the entire basin by assuming a linear relationship of altitude. As a result, it was found that the estimated N concentration coincided well with observed concentrations at six sites—the Shiramine and Kuwajima (upper stream), Nakajima (lower stream) and Dainichi dam, Tedori dam and Senami sites (middle stream). The seasonal variation of N concentrations was low in the snowmelt period and high in autumn through to winter. This was not due to the larger discharge in snowmelt season as it was also found that N deposition was high in winter and low in spring, which indicated a clear relationship between N concentration and monthly atmospheric deposition including N storage in snow pack.

Quantitative Analysis of the Rate of Geochemical Weathering of Sulfur from Sedimentary Rocks Using Atmospheric Deposition, Concentration and River Discharge Data

Quantitative analysis of the rate of geochemical weathering of sulfur (S) from sedimentary rocks (GeoS) was conducted using concentration (Cs) and discharge (Qs) data from the Tedori River and atmospheric deposition (AtdepS) in the basin. First, S fluxes were calculated using 16 years of Cs and Qs data. The annual average discharge of S (TotalS) was estimated at 8597 ton·year-1 (117.3 kg·ha-1·year-1). Of this, 1331 ton·year-1 was AtdepS (18.2 kg·ha-1·year-1) and another 7266 ton·year-1 was GeoS (99.1 kg·ha-1·year-1). Monthly changes in TotalS were investigated, which showed that GeoS was highest in summer, because of the air temperature, while AtdepS peaked in winter because of seasonal wind. Using Qs and AtdepS corrected for altitude, TotalS, AtdepS and GeoS were estimated at six sites, and among these sites we found that the TotalS per unit area values were random, depending on the site characteristics. In particular, the discharge from the Kuwajima site was remarkably high suggesting that the sedimentary rocks at this site had higher pyrite content than at the other sites. Finally, we also assessed the relationship between the characteristics of sedimentary rocks and GeoS in a range of rivers in the Hokuriku Region, and found that there was a close relationship between concentrations of SO42- greater than 10 mg·l-1 and sedimentary rocks containing the pyrite group. In addition, we estimated that the influence of GeoS was present when the concentration of SO42- in river water was greater than 2 - 3 mg·l-1 in the Hokuriku region.

Atmospheric deposition of polycyclic aromatic hydrocarbons （PAHs） in Shanghai： the spatio-temporal variation and source identification

This study investigated the dry and wet deposition fluxes of atmospheric polycyclic aromatic hydrocarbons （PAHs） in Shanghai, China. The flux sources were traced based on composition and spatio-temporal variation. The results show that wet deposition concentrations of PAHs ranged from 0.07 to 0.67 μg·L-1 and were correlated with temperature （P 〈 0.05）. Dry deposition of PAHs concentrations ranged from 3.60-92.15 μg·L-1 and were higher in winter and spring than in summer and autumn. The annual PAH average fluxes were 0.631 μg·m-2·d-1 and 4.06 μg.m·d-1 for wet and dry deposition, respectively. The highest wet deposition of PAH fluxes was observed in summer, while dry deposition fluxes were higher in winter and spring. Atmospheric PAHs were deposited as dry deposition in spring and winter, yet wet deposition was the dominant pathway during summer. Total atmospheric PAH fluxes were higher in the northern areas than in the southern areas of Shanghai, and were also observed to be higher in winter and spring. Annual deposition of atmospheric PAHs was about 10.8 t in across all of Shanghai. Wet deposition of PAHs was primarily composed of two, three, or four rings, while dry deposition of PAHs was composed of four, five, or six rings. The atmospheric PAHs, composed of four, five, or six rings, primarily existed in the form of particulates. Coal combustion and vehicle emissions were the dominant sources of PAH in the observed area of downtown Shanghai. In suburban areas, industrial pollution, from sources such as coke oven, incinerator, and oil fired power plant, was as significant as vehicle emissions in contributing to the deposition of PAHs.

Complex sources of air-soil-water pollution processes in the Miyun reservoir region

The comprehensive impact of atmospheric dry deposition and wet deposition and the pollution sources of farmlands, mining areas, and towns along the Baihe River on the water quality of Miyun reservoir is investigated from the angle of the complex sources of air-soil-water pollution processes, in the context of the 1990-2001 precipitation chemical data at Shangdianzi station--a WMO regional background air pollution monitoring station 15 km far from the Miyun reservoir, in conjunction with the atmospheric dry deposition and wet deposition data of the 2002-2003 Beijing City Air Pollution Observation Field Experiment (BECAPEX). Analysis results suggest that the major ions in precipitation in the Miyun reservoir region in this period were SO, NO, NH and Ca2+; wet acid deposition quantity of Miyun reservoir in the summer half year (April to September) was greater than the quantity in the winter half year (October to March), and the annual wet acid deposition in the reservoir exhibited a rising trend with the mean 1038.45 t, the maximum 1766.31 t occurred in 1996, and the minimum 604.02 t in 1994; the long-term averaged pH of atmospheric precipitation in the Miyun reservoir region was 5.20, i.e. weakly acidic, and the interannual variation of pH values displayed a falling trend. pH values of water body at various depths in the Miyun reservoir were all greater than 7.0, but they exhibited vertical and horizontal nonhomogeneity, and at the same region pH decreased vertically with depth; the 2002 and 2003 annual dustfalls in the Miyun reservoir were 13513.08 t and 3577.64 t, respectively, and the spring dustfall was the number one in a year, accounting for the 61.91% and 44.56% of the annual totals of 2002 and 2003, respectively. Because the atmospheric dry deposition and wet depositions contain multiple types heavy metal elements and harmful elements, they to some extent exacerbated the eutrophication, acidification and potential heavy metal pollution of the reservoir water. The above comprehensive analysis results reveal the complex source characters of the air-soil-water pollution process and the multi-sphere interaction effect. Besides, summer (rainy season) is a season when local soil pollutants enter the water system of reservoir after being washed out by torrential rain or heavy precipitation, which starts the air-soil- water chaining pollution processes, and results in the water pollution of rivers and reservoirs. It is found from the statistical analysis in this paper that the water pollution of Miyun reservoir was correlated with the rain wash-out and confluent flow in the peripheral and upstream local region of the reservoir, and the pollutant concentration of the reservoir water was significantly correlated with the upstream local region precipitation. Those correlation characters reveal the effect of the air-soil-water multi-spheric interaction of reservoir water pollution process. This paper presents the point of view of the complex source analysis of reservoir water pollution and a technical approach for tracing the spatial distribution of the upstream pollution source of the water systems of reservoir.

胶州湾大气降水水溶性离子组成特征及来源解析

基于2019年6月至2020年8月胶州湾沿岸的大气降水样品,分析降水主要水溶性离子(Na^(+)、K^(+)、Ca^(2+)、Mg^(2+)、NH^(4+)、F-、Cl^(-)、SO_(4)^(2-)、NO_(3)^(-)、MAS-(甲基磺酸根))的组成特征和湿沉降通量,评估其对近海营养成分输入的贡献和潜在生态效应,并利用气团后向轨迹和正定矩阵因子分解法(PMF)解析其主要来源.结果表明,观测期间,胶州湾大气降水雨量加权平均(Volume-weighted Mean,VWM)pH为6.41,电导率的VWM值为19.3μS/cm,降水中水溶性离子以Na^(+)、NH^(4+)、NO_(3)^(-)、Cl^(-)和SO_(4)^(2-)为主,在季节上呈现出冬春季浓度明显高于夏秋季的特征,而湿沉降通量则因受降水量的控制而主要集中在夏季(约占55%).胶州湾区域大气降水共清除7274.6t水溶性离子,营养盐(主要为NH^(4+)和NO_(3)^(-),以氮计)沉降入海量达951.9t/a,表明降水在清洁大气的同时也加剧了海洋环境的污染和海洋生态系统的失衡.气团后向轨迹分析得到了观测期间控制胶州湾降水的4类主要气团,在不同季节,降水过程受到不同气团的影响,其中以来自华东地区和东北方向的气团的影响较大.基于PMF的源解析结果显示,胶州湾大气降水水溶性离子受到农业源、海洋源、扬尘源、生物质和垃圾燃烧源、工业和交通源5种来源的共同控制,其中以农业源排放的贡献最为突出(26.7%),而其他4种源的贡献大致相当.研究证实胶州湾大气环境受到复杂人为源排放、矿物沙尘以及海洋源排放的综合制约,而人为排放的贡献占主导地位.

双通道离子色谱仪在湿沉降平衡中的应用研究

用双通道离子色谱仪同时测定湿沉降中F^(-)、Cl^(-)、NO_(3)^(-)、SO_(4)^(2-)四种阴离子和Na^(+)、NH_(4)^(+)、K^(+)、Mg^(2+)、Ca^(2+)五种阳离子。实验结果表明:四种阴离子和五种阳离子标准曲线相关系数均大于0.999,检出限均低于0.02 mg/L。相对标准偏差不大于5.7%,加标回收率范围在94.0%~104%。利用测得的九种阴、阳离子浓度,结合pH和电导率数值,计算湿沉降阴、阳离子浓度平衡和电导率平衡,均满足《酸沉降监测技术规范》(HJ/T 165-2004)要求。

Influence of specimen-reconstituting method on the undrained response of loose granular soil under static loading

This paper describes the results of an experimental study on the undrained shear behaviour of loose sand collected from the location close to the epicenter of the recent Chlef （Algeria） Earthquake （October 10,1980）.The study focuses on the effects of the mode of the soil deposition on the liquefaction resistance of the Chlef sand.For this purpose,the results of undrained monotonic triaxial compression tests performed on samples with initial density of 0.29 under initial confining pressures ranged from 50 kPa to 200 kPa are presented.The specimens were prepared by two depositional methods namely dry funnel pluviation and wet deposition.It was found that there was a marked difference in the undrained behaviour of sand in terms of maximal deviatoric stress,peak strength,residual strength and excess pore water pressure,even though the density and stress conditions were identical.The conclusion was that the soil fabric was responsible for this result.The results indicated also that at low confining pressures,the specimens reconstituted by the wet deposition method exhibited complete static liquefaction （zero effective confining pressure and zero stress difference）.

南极洲伊丽莎白公主地区主要离子沉积方式及nssSO_4^(2-)气候效应研究

通过对１９９６／１９９７年中国首次南极内陆冰盖考察获得的南极洲伊丽莎白公主地区５０ｍ 雪芯样品主要阴、阳离子浓度、通量和积累率关系的研究，揭示以下规律：１）南极洲伊丽莎白公主地区大气中各主要离子浓度足够大，足以使本地区冰雪中主要离子浓度不随积累率的变化而变化，即离子浓度不受积累率的影响。２）各主要离子干、湿沉积所占比重的计算结果表明，本地区离子沉积方式以湿沉积为主。另外，ｎｓｓＳＯ２－４ 的研究结果表明火山爆发的中、短期气候效应在伊丽莎白公主地区反应不明显。

贵州省遵义地区降水中低分子有机酸及其来源

甲酸和乙酸是大气对流层中广泛存在的低分子有机酸.降水中有机酸的研究是认识C、H、O等元素生物地球化学循环和酸雨成因的重要内容.贵州省遵义地区是我国酸雨高发地区，在遵义市进行了为期1 a的降水采集，并利用离子色谱法和原子吸收法分别对降水中主要阴离子（包括有机和无机）和阳离子进行了测定.结果显示，pH的年均值为4.11，表明遵义市酸雨形势依然严峻;甲酸和乙酸的雨量加权平均值分别为9.29μmol·L^-1（范围：0.15～46.14μmol·L^-1）和6.47μmol·L^-1（范围：0.02～19.11μmol·^L-1），占阴离子总量的4.10%，二者的相关系数达到0.86，说明甲酸和乙酸具有共同的来源.在一次降雨事件中，有机酸的浓度一般随降雨时间的延长而降低，但在降雨中后期有时会出现上升的现象，表明有机酸主要来自云下淋滤作用，少数情况下来自大气远距离的传输.遵义市区的山间盆地地形、高湿度、低风速、以尘埃为主的大气污染物等特点为有机酸来源于当地创造了条件.应用气液平衡的原理，提出了降水中甲酸、乙酸比值（F/A）aq的有机酸来源判定方法。发现遵义降水中的有机酸春季和冬季主要来自人类活动的释放，夏季和秋季则主要来自植物的释放。

重庆地区降水污染分析

通过对近 10年来重庆市国控点降水样品监测结果的分析 ,认识重庆地区降水污染特征、降水污染的现状及变化趋势 ;探讨了降水污染变化趋势与能源结构和大气污染控制措施实施效果的关系以及降水污染程度的大小与降水p H值和酸雨的关系 ,以期人们对降水污染和降水酸化有更清楚更全面的认识。

湿沉降离子平衡参数取值范围的计算

为保证湿沉降监测数据的可靠性及国际间数据的可比性，对不同类型湿沉降临测的离子平衡参数（R1）的参考值XR1，的范围进行了计算和分析。结果表明，XR1的取值主要受降水中离子组成、离子浓度以及监测准确性的影响不同类型降水的XR1的取值范围有所差别，同一类型降水的XR1也会因降水中总离子浓度的差别而不同，降水中总离子浓度（C＋A）〉100μeq／L时，海陆相间型降水的XR1的取值范围为5％～7％；内陆型降水的XR1的取值范围为5％～9％；海洋型降水XR1的取值范围为5％～11％，当（C＋A）〈50μeq／L时，总离子浓度越小，实验的精密度越差，离子浓度的精密度（αi）值越大．当αi取100％时，XR1的取值范围为33％-71％，国际间同类降水监测规范比较，（C＋A）≥50μeq／L时，R1的取值基本在XR1的计算范围内；而（C＋A）〈50μeq／L时，各个标准之间的差别较大。

上海市近16年湿沉降化学特征分析

对上海市1992-2007年湿沉降监测结果进行研究,16年来,上海市湿沉降主要呈现以下特征:pH总体呈现下降趋势,酸雨频率呈现上升趋势;2002年起升幅很大;硫酸根离子和钙离子浓度总体呈下降趋势,2003年后,各离子浓度都有一定程度下降;钙离子在总阳离子中的比例总体上明显下降,铵离子与总阳离子的百分比总体上呈上升趋势;硫酸根离子在总阴离子中的比例有所下降,硝酸根离子与总阴离子的百分比则一直呈上升趋势;硫酸根与硝酸根年均值的比值总体上呈明显的下降趋势,表明硫酸型在逐渐减弱;钙离子与铵离子的比值总体上也呈明显的下降趋势。