长三角区域背景地区降水化学特征

为了解临安降水的化学特征及主要致酸组分,2008年5-11月在临安区域大气本底站采集了35个降水样品,分析其化学组分.结果表明,临安地区降水中无机阴阳离子体积加权平均浓度比我国城市地区低,但个别降水中无机离子浓度总量会很高;降水中Cl-和K+主要来自海洋源的贡献;SO42-,Ca2+和Mg2+主要来自非海洋源;燃煤排放产生的SO42-仍然是临安地区降水酸化的主要无机致酸组分,35场降水中,平均占到无机阴离子总量的52%,NO3-对临安降水酸化具有重要贡献,反映出长三角区域快速城市化过程中机动车数量快速增长对区域大气环境的影响在增强.     

中国大气酸沉降与土壤酸化问题

我国对大气酸沉降的研究起自７０年代末．以酸雨研究占主导地位。我国酸雨现象区域性、发展性强，在地理上以南方酸性土壤地区为主，在成分上以硫酸盐型酸雨为主；无论是酸度还是频率，酸雨都是极严重的生态环境问题。酸沉降已对农、林生态系统生产产生了严重的破坏效应，但其累积性的环境化学反馈却未引起人们的足够重视。我国酸雨地区以强酸性富铝土壤为主，对大气酸沉降有较大的敏感性。应用β指标还表明，酸沉降可使南方主要土壤因酸化而在３０—６０年内降低ｐＨ一个单位。近年来对酸沉降诱发的土壤酸化研究以模拟降水的土柱试验为主，从ｐＨ下降、盐基淋出、Ａｌ及重金属移动等方面来提示出酸沉降可能对土壤产生的化学影响。但作为过程化学研究，其案例监测研究的报道尚很少。对于南方严重的酸雨现象，应加强实地动态监测和过程分析，注重Ａｌ化学及其对环境的反馈，将酸沉降对生态系统的破坏提高到生态毒理机制上。     

无机阴离子对镉、铅解吸特性的影响

土壤中重金属的解吸直接影响重金属在环境中的形态转化和植物有效性.而地表水环境及土壤中的无机阴离子能与重金属离子络合,影响重金属在环境中的迁移和作物的吸收.因此,有关无机阴离子对重金属解吸特性影响的研究,将有利于了解重金属的吸附-解吸机制及其控制措施.文章以我国东北地区草甸棕壤作为研究对象,采用静态解吸实验研究无机阴离子(C1-、SO42-、F-)对土壤中镉、铅的解吸行为的影响.结果表明,土壤中镉、铅的解吸率与无机阴离子类型、浓度密切相关;随着解吸液中无机阴离子(C1-、SO42-、F-)浓度的增大,土壤镉、铅的解吸率随之提高.C1-、SO42-、F-这3种无机阴离子对解吸土壤中镉的影响力顺序是:C1- > SO42- > F-;对解吸土壤中铅的影响力顺序是:SO42- >C1- > F-.     

太湖北部流域水化学特征及其控制因素

为了解太湖北部流域主要河网区水质受该流域地质状况、岩石和土壤的化学风化作用以及人类活动的影响等方面,对太湖北部流域河网区主要河道水体中的主要离子进行了采样研究。结果表明:太湖北部流域水体中的TDS平均值为355.74mg·L-1,变化范围为276.08～681.54mg·L-1,其中Ca2+和HCO3-是占绝对优势的离子,分别占阳离子和阴离子总量的46.2%和48.9%;其次是Na+和SO42-,分别占阳离子和阴离子总量的35.9%和27.5%。进而判断出该流域水化学类型是以碳酸盐岩石和蒸发岩来源为主的HCO3--Ca2+-Na+型。再从离子的自然起源和人类活动角度分别对水化学类型的控制因素进行分析,一方面利用吉布斯分布模式投点作图得出结论:其离子自然起源的优势机制是岩石的风化作用,而蒸发-结晶和大气降水的输入作用十分微弱,这与该流域的水文、地理、地质背景相一致;另一方面通过SPSS软件的相关关系分析得出结论:NO3-、SO42-、K+、Ca2+和Mg2+的相关性较强,与Cl-也呈正相关,说明水体中这些主要离子都具有共同的来源,其中NO3-的较高含量(平均值为14.74mg·L-1)反映了该流域受人类影响较大。尤其是NO3-与SO42-的相关性达到0.83,再次说明氮污染对该流域水体的酸化和水质变化有较大影响。     

温州红壤的酸沉降临界负荷研究

本文简要介绍了以碱总量守恒为基础建立的兼能描述钙质与非钙质土壤长期酸化过程的动态模型（ＬＴＳＡＭ）,并利用该模型讨论了温州红壤的酸沉降临界负荷。结果表明,以硫沉降即酸沉降的硫沉降非酸沉降两观点分别来确定红壤的临界负荷,其值依次为３．９１与１．８４ｇ·ｍ＾－２·ａ＾－１,后者仅是前者的４７％,差异显著应加以区别。     

太湖北部流域水化学特征及其控制因素

为了解太湖北部流域主要河网区水质受该流域地质状况、岩石和土壤的化学风化作用以及人类活动的影响等方面,对太湖北部流域河网区主要河道水体中的主要离子进行了采样研究。结果表明：太湖北部流域水体中的TDS平均值为355．74mg·L-1,变化范围为276．08--681．54mg·L-1,其中ca2＋和HCO3-是占绝对优势的离子,分别占阳离子和阴离子总量的46．2％和48．9％;其次是Na＋和SO42-,分别占阳离子和阴离子总量的35．9％和27．5％。进而判断出该流域水化学类型是以碳酸盐岩石和蒸发岩来源为主的HCO3-Ca2＋-Na＋型。再从离子的自然起源和人类活动角度分别对水化学类型的控制因素进行分析,一方面利用吉布斯分布模式投点作图得出结论：其离子自然起源的优势机制是岩石的风化作用,而蒸发一结晶和大气降水的输入作用十分微弱,这与该流域的水文、地理、地质背景相一致;另一方面通过SPSS软件的相关关系分析得出结论：NO3-、SO42-、心、ca2＋和Mg2＋的相关性较强,与cl‘也呈正相关,说明水体中这些主要离子都具有共同的来源,其中NO3-的较高含量（平均值为14．74mg·L-1）反映了该流域受人类影响较大。尤其是NO3-与sO42-的相关性达到0．83,再次说明氮污染对该流域水体的酸化和水质变化有较大影响。     

施用尿素和硫酸铵对红壤硝化和酸化作用的影响

通过室内恒温培养试验,研究施用CO(NH2)2和(NH4)2SO4对初始pH值分别为5.14、4.77和4.34的红壤酸化速率和硝化速率的影响。结果表明,施用CO(NH2)2显著增加了3种红壤的硝化速率,从而显著加速土壤酸化。培养结束时,3种红壤pH值较培养过程中最高值分别下降2.14、1.23和0.56。施用(NH4)2SO4抑制了初始pH<5.0的2种红壤的硝化作用,从而显著降低这2种红壤的硝化速率和酸化速率,但显著增加了初始pH>5.0红壤的硝化速率,对其酸化速率则未见显著影响。3种红壤的酸化速率与硝化速率间存在显著线性相关关系。硝化作用是导致农田红壤pH值下降的主要原因之一,但不同氮肥对红壤硝化速率和酸化速率的影响不同。     

硫氮沉降下西北荒漠煤矿区周边土壤性质的变化特点

近年来中国大部分区域大气硫、氮沉降速率趋于平稳甚至下降,但西北地区煤炭行业的快速发展使得硫、氮沉降速率加快.燃煤电厂作为酸前体物的主要排放源之一,在其周围开展硫、氮沉降效应研究,可为合理评价煤矿区大气污染物控制措施的实施效果提供数据支撑.该文以宁东能源化工基地3个燃煤电厂为采样点,研究了电厂周围土壤化学和生物学性质的变...     

伴随阴离子对土壤Cd形态转化的影响

化学性质各异的伴随阴离子通过影响进入土壤的外源Cd2+后的形态转化,而影响其迁移特性和生物毒性。对此进行了解将有助于采取相应的防治镉污染的技术措施。通过室内连续培养试验(0~70 d),研究了伴随阴离子(NO3-、C1-、SO42-)对Cd2+在土壤中的吸附特性、形态分配与转化特性的影响。结果表明,伴随阴离子对添加外源Cd2+溶液后的土壤Cd吸附作用能力表现为:SO42-NO3-C1-;SO42-处理在20 d时吸附率达最大值(93.61%);NO3-与C1-处理在30 d时吸附率达最大值,分别为82.25%、67.97%。初始状态土壤中Cd主要以残渣态存在,可交换态Cd含量与比例最低,占总Cd含量不到10%。添加1.0 mmol·L-1外源Cd2+处理后,在培养期内(0~70 d),表现为可交换态Cd含量铁锰氧化物结合态Cd含量碳酸盐结合态Cd含量残渣态Cd含量有机结合态Cd含量。土壤可交换态Cd在0~70 d分配系数达到38%~61%,其中SO42-处理培养10 d达到最大值(61.09%),NO3-与C1-处理30 d时达到最大值(分别为43.74%和41.80%)。土壤碳酸盐结合态Cd含量在30 d时趋于饱和,其含量(0~70 d)表现为SO42-C1-NO3-。3种伴随阴离子处理的土壤铁锰氧化物结合态Cd含量在0~50d无显著性差异。有机结合态Cd和残渣态Cd含量随着培养周期延长而逐渐增加,但其吸收转化分配比例相对可交换态、碳酸盐结合态和铁锰氧化物结合态低。从生物利用度系数来评价镉形态的危害程度,初始状态土壤中其危害程度表现为生物潜在可利用态生物难利用态生物易利用态。添加1.0 mmol·L-1的外源Cd2+溶液后,SO42-处理的表现为:生物易利用态生物潜在可利用态生物难利用态;C1-和NO3-处理的表现为生物潜在可利用态生物易利用态生物难利用态。这表明,镉形态在SO42-处理伴随下对土壤造成的危害程度相对C1-和NO3-处理严重。外源Cd2+溶液进入土壤主要转化为可交换态Cd(SO42-NO3-C1-),SO42-处理培养10 d达到最大值(转化系数为61.09%)。可交换态Cd在土壤中具有较强的迁移性,容易被生物吸收利用,对环境影响最大。     

土壤酸化对油松生长的影响

褐色森林土酸化后,pH值下降,同时淋溶出大量Al离子和Mn离子。播种在酸化土壤中的油松种子萌发率稍有提高。生长在酸化土壤的油松苗的叶绿素含量,蒸腾强度,光合速率,相对生长率和干重均下降,原因是Al离子和Mn离子对油松的有毒害作用,并且阻止油松对钙离子和镁离子的吸收。表3参12     

Atmospheric deposition, mineralization and leaching of nitrogen in subtropical forested catchments, South China

In recent years, China has conducted considerable research focusing on the emission and effects of sulphur (S) on human health and ecosystems. By contrast, there has been little emphasis on anthropogenic nitrogen (N) so far, even though studies conducted abroad indicate that long-range atmospheric transport of N and ecological effects (e.g. acidification of soil and water) may be significant. The Sino-Norwegian project IMPACTS, launched in 1999, has established monitoring sites at five forest ecosystems in the southern part of PR China to collect comprehensive data on air quality, acidification status and ecological effects. Here we present initial results about N dynamics at two of the IMPACTS sites located near Chongqing and Changsha, including estimation of atmospheric deposition fluxes of NOx and NHx and soil N transformations. Nitrogen deposition is high at both sites when compared with values from Europe and North America (25-38 kg ha(-1) yr(-1)). About 70% of the deposited N comes as NH4, probably derived from agriculture. Leaching of N from soils is high and nearly all as NO3-. Transformation of N to NO3- in soils results in acidification rates that are high compared to rates found elsewhere. Despite considerable leaching of NO3- from the root zone of the soils, little NO3- appears in streamwater. This indicates that N retention or denitrification, both causing acid neutralization, may be important and probably occur in the groundwater and groundwater discharge zones. The soil flux density of mineral N, which is the sum of N deposition and N mineralization, and which is dominated by the N mineralization flux, may be a good indicator for leaching of NO3- in soils. However, this indicator seems site specific probably due to differences in land-use history and current N requirement.     

酸雨对外来植物入侵的影响

酸雨和外来种入侵都是全球关注的问题。结合外来入侵植物的生态适应特性以及酸雨的危害特征,系统分析了酸雨对外来植物入侵产生的影响。酸雨对外来植物入侵的影响是复杂多样的。酸雨导致群落冠层稀疏,群落透光率增加,加之氮沉降后土壤、水体氮素的增加,有利于生长力强的外来喜阳植物入侵;酸雨加速土壤酸化,促使基本离子淋失以及A1毒等危害植物的生长发育,植物的内源激素以及化感作用发生改变,适应力和耐受力强的外来植物在与本地植物竞争中处于相对优势而成为入侵种;酸雨以及外来植物入侵改变了土壤微生物群落结构,影响本地植物的生长而促使外来植物的入侵。     

常州市酸雨化学特征及其与大气污染物的关系

收集了常州市2008年全年的56次降水,并分析了它们的9种主要离子的浓度及pH值。全年降水的pH雨量加权平均值为4.76。降水酸度和大气中气态污染物及可吸入颗粒物呈正相关性。气态污染物及可吸入颗粒物的冲刷净化直接影响降水的pH值及其化学成分。SO42-、NO3-、Ca2＋和NH4＋是影响降水pH值的主要离子。常州市2008年的降水主要酸性离子SO42-和NO3-浓度明显高于我国降水背景点纳木错,但低于其他部分城市,表明常州市的大气环境受到了明显的人为污染,但污染程度相对较轻。常州市的环境空气质量在近20年内得到了明显的改善。     

A study on major inorganic ion composition of atmospheric aerosols

Atmospheric aerosol samples were collected from Akola and Buldana region covering around 40 sqkm area during October-November 2002 and were analyzed for ten major inorganic ions namely F-, Cl-, NO3-, SO4(2-), PO4(2-), Na+, K+, Ca2+, Mg2+ and NH4+ using ion chromatographic technique. The average mass of aerosols was found to be 225.81 microg/m3 with standard deviation of 31.29 and average total water soluble load of total cations and anions was found to be 4.32 microg/m3. The concentration of ions in samples showed a general pattern as SO4(2-) > NO3- > Cl- > PO4(2-) > F- for anions and Na+ > Ca2+ > NH4+ > Mg2+ > K+ for cations. The overall composition of the aerosols was taken into account to identify the sources. The trend showed higher concentration of sodium followed by calcium, sulfate, nitrate, phosphate and ammoinum and found to be influenced by terrestrial sources. The presence of SO4(2-) and NO3- in aerosols may be due to re-suspension of soil particles. Ca2+, Mg2+ and Cl- are to be derived from soil materials. The presence of NH4+ may be attributed to the reaction of NH3 vapors with acidic gases may react or condense on an acidic particle surface of anthropogenic origin. The atmospheric aerosol is slightly acidic due to neutralization of basicity by SO2 and NO(x).     

珠江三角洲城市雨水的化学组成及其成因探讨

于2005—2007年间,基于降水过程监测分析了广州市和珠海市雨水的化学组成。结果表明,广州市雨水的pH值变化于3.32~7.03之间,平均值为4.35,众数约为4.15。珠海市雨水的pH值变化于3.38~6.49之间,平均值为4.51。雨水pH值随降水强度的减弱而降低,这决定于大气中水汽与酸性气体的接触时间。珠江三角洲城市雨水中所含主要离子依次是SO42-、NO3-、NH4＋、Ca2＋、Cl-。雨水的酸化与降水过程密切相关。降雨初期雨水比中后期雨水的pH值高,揭示降雨初期大气中的粉尘颗粒有效中和雨水的酸度。多天连续降水天气对大气尘埃的清洗作用明显,但是持续的SO2和NOx排放更容易使雨水酸化。滨海城市降水初期雨水的电导率上升较快（可以从小于1μS.cm-1上升到20~30μS.cm-1）,随着降水时间的延长雨水的电导率以较慢的速率上升。     

北京市大气PM_（2.5）中四种水溶性阴离子的水平变化比较

了解北京市城区和郊区大气细颗粒物中的四种水溶性阴离子F-、Cl-、SO42-、NO3-的浓度水平,并分析影响其水平高低的因素。使用聚四氟乙烯滤膜分别采集北京市城区和郊区大气中的PM2.5,用纯水提取后采用离子色谱法测定水溶性阴离子质量浓度。采样期间北京市大气PM2.5、F-、Cl-、SO42-和NO3-质量浓度几何均数分别为55.36、0.02、0.46、6.72和1.09μg·m-3,四种水溶性阴离子质量浓度总和占PM2.5质量浓度的19.14%;同一季节（春季）郊区监测点大气PM2.5、SO42-和NO3-质量浓度显著高于城区监测点;城区大气PM2.5与四种水溶性阴离子质量浓度秋季高于春季,但差异无统计学意义;大气PM2.5与Cl-、SO42-和NO3-质量浓度均高度相关。Cl-、SO42-、NO3-是北京市大气PM2.5的重要组成成分。     

北京市大气PM2.5中四种水溶性阴离子的水平变化比较

了解北京市城区和郊区大气细颗粒物中的四种水溶性阴离子F-、Cl-、SO42-、NO3-的浓度水平,并分析影响其水平高低的因素。使用聚四氟乙烯滤膜分别采集北京市城区和郊区大气中的PM2.5,用纯水提取后采用离子色谱法测定水溶性阴离子质量浓度。采样期间北京市大气PM2.5、F-、Cl-、SO42-和NO3-质量浓度几何均数分别为55.36、0.02、0.46、6.72和1.09μg·m-3,四种水溶性阴离子质量浓度总和占PM2.5质量浓度的19.14%;同一季节(春季)郊区监测点大气PM2.5、SO42-和NO3-质量浓度显著高于城区监测点;城区大气PM2.5与四种水溶性阴离子质量浓度秋季高于春季,但差异无统计学意义;大气PM2.5与Cl-、SO42-和NO3-质量浓度均高度相关。Cl-、SO42-、NO3-是北京市大气PM2.5的重要组成成分。     

A Comparison of the Short-Term Dynamics of Soil “Damage” Due to Enhanced Nitrogen Deposition As Ammonium Sulphate Or Nitric Acid

An experiment has been conducted to contrast the effects of enhanced oxidised and reduced nitrogen deposition upon key chemical parameters in a Calluna moorland podzol. A 40 cm deep podzol profile, derived from granite, was reconstructed in one hundred 4.2 cm diameter cores. for 20 weeks, the cores were subjected twice weekly to simulated rainfall containing either twice ambient nitrogen deposition in Aberdeen, or further enhanced nitrogen (further 2- and 6-fold increases) as nitric acid or ammonium sulphate. to quantify the dynamics of soil change in each horizon, randomly selected cores were destructively analysed every two weeks and the soils analysed. Increased nitrogen inputs, regardless of form, substantially and immediately reduced surface soil pH_water via the mobile anion or salt effect. for the higher nitrogen treatments, the pH reduction was seen throughout the profile. Longer term soil acidification was also seen in the pH_{calcium chloride} results over the 20 weeks. at a given nitrogen deposition rate, the effects of ammonium sulphate and nitric acid on soil pH_{calcium chloride} were similar. the ammonium sulphate treatments were especially effective at reducing base saturation throughout much of the profile, the direct base cation leaching being associated with substantial ammonium accumulation. the results suggest that the direct base cation leaching caused by ammonium deposition needs to be considered when assessing atmospheric pollution “damage” to heathland soils.     

Atmospheric Deposition, Mineralization and Leaching of Nitrogen in Subtropical Forested Catchments, South China

In recent years, China has conducted considerable research focusing on the emission and effects of sulphur (S) on human health and ecosystems. By contrast, there has been little emphasis on anthropogenic nitrogen (N) so far, even though studies conducted abroad indicate that long-range atmospheric transport of N and ecological effects (e.g. acidification of soil and water) may be significant. The Sino-Norwegian project IMPACTS, launched in 1999, has established monitoring sites at five forest ecosystems in the southern part of PR China to collect comprehensive data on air quality, acidification status and ecological effects. Here we present initial results about N dynamics at two of the IMPACTS sites located near Chongqing and Changsha, including estimation of atmospheric deposition fluxes of NO_x and NH_x and soil N transformations. Nitrogen deposition is high at both sites when compared with values from Europe and North America (25–38 kg ha^–1 yr^–1). About 70% of the deposited N comes as NH₄, probably derived from agriculture. Leaching of N from soils is high and nearly all as NO₃ ^–1. Transformation of N to NO₃ ^–1 in soils results in acidification rates that are high compared to rates found elsewhere. Despite considerable leaching of NO₃ ^–1 from the root zone of the soils, little NO₃ ^–1 appears in streamwater. This indicates that N retention or denitrification, both causing acid neutralization, may be important and probably occur in the groundwater and groundwater discharge zones. The soil flux density of mineral N, which is the sum of N deposition and N mineralization, and which is dominated by the N mineralization flux, may be a good indicator for leaching of NO₃ ^–1 in soils. However, this indicator seems site specific probably due to differences in land-use history and current N requirement.     

湘南红壤对NO_3~-和SO_4~(2-)的吸附机理研究

本文研究了湘南第四纪红粘土发育的红壤对NO_3和SO_4~(2-)的吸附等温线。结果表明红壤对NO_3~-的吸附在浓度低时为负吸附,浓度高时为正吸附,吸附机理为非专性吸附,红壤对SO_4~(2-)的吸附等温式以Freundlich方程最好,在达到最大吸量(X_m)之前,SO_4~(2-)以置换羟基(—OH)的配位吸附为主;而在达到最大吸附量以后,以非专性物理吸附为主。