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1.
松嫩平原西部盐沼湿地水环境化学特征   总被引:10,自引:1,他引:9  
邓伟  何岩  宋新山  阎百兴 《地理研究》2000,19(2):113-119
松嫩平原西部盐沼湿地水环境碱化程度高,水中的pH值普遍高于8.0,多数为苏打钠型水。在对本区盐沼基本水环境化学特征阐述的基础上,通过对水化学的基本变量CO32-、HCO32-、Cl-、Ca2+、Mg2+、SO42-、Na+和派生变量(Cl-+SO42-)/HCO32-及Na+/(Ca2+ Mg2+)等的相关分析,得出各水化学变量之间的相关关系,并以pH值为分类基础得到了判别函数和判别区域图,对区域盐沼湿地水环境化学特征的研究方法作出了有意义的尝试。  相似文献   

2.
内蒙古西部地区盐湖水化学特征   总被引:3,自引:1,他引:2       下载免费PDF全文
2008年9~10月和2009年9月对内蒙古西部地区14个盐湖进行了考察、采样和分析。研究发现,本区盐湖卤水主要离子含量顺序为Na+>Cl->SO2-4>Mg2+>K+,次要离子为Ca2+ >HCO-3>CO2-3,微量元素为B2O3>Br->Li+。Na+的分布特征为东部高,北部中等,西南部偏低;而Cl-为东高西低;K+大致为南高北低;Mg2+为中部高,西部低,北部与南部中等。SO2-4、 Ca2+和CO2-3的区域分布特征均不明显;微量元素Li+ 、Br-、B2O3含量虽局部(两大沙漠连接带)有所富集,但绝对含量不高。对天然盐湖和人工采盐池的卤水进行了对比。采盐池中卤水因为蒸发强烈,离子浓度显著高于天然盐湖。分析天然盐湖与采盐池卤水离子浓度的变化规律发现,卤水蒸发初期Na+、Cl-、SO2-4离子浓度随矿化度的升高而增大,Ca2+离子浓度明显下降,卤水蒸发后期Mg2+、K+大量富集,整个卤水蒸发过程中微量元素Li+与B2O3浓度一直随矿化度的升高而增大。这些结果对内蒙古西部盐湖的研究与开发都具有积极意义。  相似文献   

3.
柴达木盆地是一个典型的大陆成盐成钾盆地,盆地西部大盐滩矿区有着丰富的地下卤水资源,具有开发利用的远景。通过野外实地考察,采集大盐滩矿区不同深度(9.8m--133m)晶间卤水样品10件,油田水样品10件,分析了卤水水化学组成和氢氧同位素值。结果表明,晶间卤水矿化度较高(平均为363.94g/L),Na+、Cl-含量较高,同时富K+、Mg2+、SO42-,贫Ca2+,B、Li、Br、Sr等元素普遍富集,水化学类型为硫酸镁亚型;油田水矿化度较低(平均为39.02g/L),Na+、Cl-含量占绝对优势,同时富Ca2+,贫Mg2+、SO42-、HCO3-,B、Sr含量较高,Li、Br含量较低,水化学类型为氯化物型。结合离子含量和水化学特征系数(钠氯系数和溴氯系数),揭示了大盐滩矿区晶间卤水主要为大气降水汇聚后经蒸发作用形成,深层晶间卤水(30m--133m)具有大气降水盐岩溶滤成因及受具有深部来源性质油田水补给的特征。氢氧同位素结果表明,卤水均发生了明显的“氢氧同位素正漂移”现象,深层晶间卤水(30m--133m)的δ18O、δD值异常偏高,推断其与经过强烈蒸发浓缩作用的浅层晶间卤水(9.8m--11.5m)以及大气降水溶滤盐岩沿断裂下渗补给有关。  相似文献   

4.
以察尔汗盐湖达布逊区段补水溶采区为研究区,靠近补水渠的D01、D03以及D05水文观测孔地下卤水为研究对象,通过水化学、相图等分析方法,研究了地下卤水在固液转化过程中水化学的时空变化特征及其影响因素。研究结果表明,储卤层中卤水化学特性在空间上具有明显差异性。在纵向上,随深度增加Na+、SO42-浓度、pH值降低,而Mg2+、Cl-、HCO3-、Li+、B3+浓度、TDS和比重升高;在横向上,D01孔中卤水具有较高的Na+、SO42-、HCO3-、Li+浓度、pH值以及较低的TDS和比重;D03孔中卤水具有较高的K+、B3+浓度;D05孔中具有较高的TDS、比重、Mg2+、Ca2+、Cl-以及Sr2+浓度。揭示了卤水在盐层中的滞留时间、盐层渗透性差异、矿物组合与分布及温度变化是影响地下卤水水化学分布特征的主要因素,并初步研究认为补水溶矿具有局限性,D01孔受补水影响最大,D03孔次之,D05孔受补水影响较弱。  相似文献   

5.
四苯硼钠—季铵盐质量滴定法分析钾含量研究   总被引:1,自引:1,他引:0       下载免费PDF全文
依据四苯硼钠—季铵盐容量法滴定K+离子的原理,采用质量滴定法,考察了滴定速度、松节油加入量对四苯硼钠与季铵盐反应的影响及共存离子(包括Li+、Mg2+、Ca2+、SO2-4、B4O2-7、CO2-3)对K+含量测定结果的影响。当测定K+离子含量在5~15 mg范围内,松节油最佳加入量为25滴,分析误差< 0.3%。  相似文献   

6.
为研究内陆盐沼植物群落的分布对土壤盐分的响应特征,选取鄂尔多斯盐湖盐沼区作为研究区,筛选了肉质耐盐植物群落,苔草植物群落和禾草植物群落3类典型植物群落,开展了土壤含水量、pH、电导率以及Na+,K+,Mg2+,Ca2 +,Cl-、SO42-、CO32-和HCO3-的测定,分析了区内典型植物群落对土壤水盐因子的响应规律。探讨了3类植物群落之间土壤因子含量的差异性;采用相关性分析和CCA分析,评价了3类植物群落多样性及物种分布随土壤因子的变化规律。结果表明,区内3类植物群落中,土壤盐分含量表现为肉质耐盐植物群落最高,苔草植物群落最低,禾草植物群落居中;植物多样性与土壤中含量最高的Na+和SO42-的相关性最显著;植物分布同时受到土壤盐分、水分和pH的显著影响。研究结果可为鄂尔多斯盐湖区土壤盐渍化改良和植被恢复提供理论支撑。  相似文献   

7.
东台吉乃尔盐湖基本地质特征及锂的分布规律研究   总被引:2,自引:2,他引:0       下载免费PDF全文
东台吉乃尔盐湖位于柴达木盆地中部,是我国众多盐湖中富含Li和B的盐湖之一。该湖与西台吉乃尔盐湖、一里坪盐湖和察尔汗盐湖别勒滩段构成了中国最大的现代盐湖锂矿床分布带。该湖地下晶间卤水分为上下两层,即Ⅰ、Ⅱ两个卤水矿层。化学组分,阴离子以Cl-为最高,其次是SO2-4、CO2-3、HCO-3;阳离子以Na+为最高,依次为Mg2+、K+、Ca2+;化学类型属硫酸盐型硫酸镁亚型。湖区水体主要由来自南部昆仑山脉的东台吉乃尔河补给。根据1998年在该盐湖的工作和前人的地质资料,对2000年前东台吉乃尔盐湖的湖区地貌、卤水的化学组成、Li的分布规律以及成盐年代进行了初步研究和探讨。  相似文献   

8.
盐碱荒地开垦年限对表层土壤盐分的影响   总被引:9,自引:0,他引:9  
周丽  王玉刚  李彦  黄刚 《干旱区地理》2013,36(2):285-291
 以典型荒漠区原生盐碱荒地及开垦农田为研究对象,通过对比研究,以阐明原生盐碱荒地开垦后不同管理措施下土壤可溶盐总量的变化规律,开垦后土壤剖面中可溶盐总量的垂直分布和季节变化规律。结果表明:开垦显著降低了0~50 cm土壤的可溶性盐含量,开垦达100 a以上老耕地的可溶性盐含量(2.31 g/kg)仅为原生盐碱荒地(26.62 g/kg)的11%;长期的耕作改变了土壤可溶性盐分在土层中的分布,原生荒漠土壤盐分具有鲜明的表聚特征,0~30 cm土层的盐分含量占整个土壤剖面的79%,开垦50 a后,土壤中的盐分分布趋于均匀,各离子浓度的垂直分布不再明显;开垦使土壤中的盐分离子组成也发生了变化,Cl-、K+、Na+离子浓度降低,而SO42-、Mg2+、Ca2+离子浓度增加,耕作层土壤由SO4-2-Cl-1盐土转变为Cl-1-SO4-2盐土;盐碱荒地土壤可溶盐浓度伴随着降水变化具有显著的季节变化特征,而季节对开垦耕地没有显著影响。总体而言,盐碱荒地经过多年开垦利用后,土壤可溶性盐分和pH值均显著降低。  相似文献   

9.
柴达木盆地西部背斜构造深层卤水资源勘查和评价成果显示,第三系背斜构造赋存深层卤水,具有良好的资源成矿条件,且潜力大。采集柴达木盆地中西部(一里坪拗陷和三湖拗陷)9处背斜构造深层卤水,分析了其水化学特征与成因。结果表明,深层卤水矿化度一般低于150 g/L,水化学类型均为氯化物型;K+、Na+、Mg2+含量较低,不具找矿价值;而B2O3、Li+含量普遍高于评价指标,Br-、I-含量普遍高于综合评价指标,为主要成矿元素;卤水的元素特征系数和分布规律及微量离子组成揭示,深层卤水是大气降水溶滤盆地周缘岩浆岩和火山岩及火山热泉的补给后,汇入古近纪—新近纪湖盆经蒸发浓缩封存在地层中的沉积卤水。  相似文献   

10.
Li+,Na+,K+/Cl-,SO2-4-H2O五元体系相图对于硫酸钠亚型富锂卤水分离提取锂盐、锂辉石加工利用和锂盐产品的开发利用工艺制定都有指导作用。20世纪50年代曾有人研究过这一体系25 ℃时的相图,限于当时的科研水平,液相组成确定不准确,对平衡固相的判断,后来诸多研究结果证明也有错误。50多年来再没有人研究这一五元体系相图。利用我们提出的Li+,Na+,K+/Cl-,SO2-4-H2O六元体系热力学模型,对该五元体系的平衡溶液组成和正确的平衡固相进行理论预测,给出了该体系的完整相图。结合硫酸锂混盐分离、加工实例阐述了该五元体系相图的应用。  相似文献   

11.
The chemistry of major cations (Mg2+, Ca2+, Na+, and K+) and anions (HCO3 , SO4 2−, and Cl) in the water of Lake Pumayum Co and its inflow river was studied, revealing the obvious ionic difference among various inflow rivers and the lake. The chemical type of the lake water was Mg2+-Ca2+-HCO3 -SO4 2+, but the major ions of the main inflow rivers were Ca2+-Mg2+-HCO3 . In the lake inlet of Jiaqu River, the main inflow river, there was significant variance of water chemistry within the depth less than 2 m. However, it was almost homogeneous at other area of the lake. Therefore, with the evidence of distribution of water chemistry and oxygen isotope of lake water, a conclusion can be outlined that Jiaqu River had a distinct effect on the hydrochemistry of the water on the submerged delta, whereas this is not the case for other rivers. The Gibbs plot revealed that the dominant mechanism responsible for controlling chemical compositions of the lake water was rocks weathering in the drainage area. Ion ratios and ternary plots further explored the main processes controlling the water chemistry of the catchment, i.e., carbonate weathering, pyrite weathering, and silicate weathering. The different hydrochemistry characteristics between river water and lake water may result from the CaCO3 precipitation. The findings will benefit the explanation of the environmental significance of carbonate in paleolimnological studies in the lake.  相似文献   

12.
Rivers and streams originating in the surrounding mountainous area are the major sources of salt in the Salinas Grandes basin (Córdoba, Argentina). These rivers infiltrate when they reach the sandflat or in the fringes of the mudflat, feeding springs which often form shallow lakes. Presently, the lakes are distant from the playa edge, thus allowing inflow waters to dissolve ancient (Pleistocene?) evaporite beds. In the sandflat environment, two dominant types of water have been recognized (SO 4 2? -Cl?-HCO 3 ? -Na+, and Cl?-SO 4 2? -HCO 3 2? -Na+), both considered as original members of the brine in the saline complex. Two main sources of solutes were distinguished, one related to the waters supplied by the southern sector and another to waters of the eastern sector. As a result of the chemical evolution in the playa environment, all brines belong to the neutral type (Cl?-SO 4 2? -Na+). Following Hardie and Eugster's (1970) model, waters from the southern sector should evolve towards an alkaline brine (Cl?-SO 4 2? -HCO 3 ? -Na+), whereas those from to the eastern sector should evolve towards a neutral one (Cl?-SO 4 2? -Na+). A computer simulation was carried out to model the chemical evolution of source waters. The results obtained by this methodology showed the same dichotomy (alkaline vs. neutral) established by Hardie and Eugster's (1970) model. The deficit in alkalinity could not be explained by any of the mechanisms published until now. Gypsum dissolution is the most likely mechanism which accounts for the chemical evolution of the waters investigated. When such a process is included in the computations, the Ca2+ supplied by gypsum beds generates an increase in the ion activity product (aCa+2·aCO 3 2? ) and produces a significant change in the 2Ca+2/(2CO 3 2? +HCO 3 ? ) ratio, switching from values less than 1 to values greater than 1. This process determines the precipitation of calcite, and leads to a decrease in alkalinity, which in turn would explain the existence of a neutral brine in the saline complex. An intermediate salinity brine was detected in the mudflat, which, according to the model (Hardie and Eugster, 1970), should evolve towards a SO 4 2? -free neutral brine (Cl?-Na+-Ca2+). The absence of this type of brine may be explained through mixing processes.  相似文献   

13.
中国内陆干旱、半干旱区苦咸水分布特征   总被引:1,自引:0,他引:1  
通过大量野外调查、水样采集和化验分析,对中国内陆干旱、半干旱区的苦咸水和高氟水分布特征进行了初步研究。采集到的地表和地下水样中,分别有51.0%和41.5%属于苦咸水;55%和59%水样氟化物含量超标,属于高氟水。研究区的苦咸水以Cl--Na+和HCO-3-Na+为主要离子类型,SO2-4-Mg2+和SO2-4-Ca2+为次要离子类型。苦咸水和高氟水主要分布在内陆河流域下游尾闾、封闭内流区低洼湖盆低地、北部准平原化干燥剥蚀低山残丘间冲积洼地、沙漠低洼湖盆和黄土高原中西部径流系数较小的河流及部分露头潜水等区域,并具有区域富集性分布特点。季节性降水、季节性河流或渠系灌溉对苦咸水的季节性或年际间变化和空间分布有较大影响。较高浓度基质含盐量、水文地质结构、气候条件和特定的水文地球化学环境是苦咸水和高氟水形成与富集分布的主要原因。  相似文献   

14.
Salinity and sodicity of groundwater are the principal water quality concerns in irrigated areas of arid and semi-arid regions. The hydrochemical characteristics and sodicity of groundwater in the Shirin Sou area, western Iran were investigated in this study by chemical analyses of groundwater samples from 49 wells. Chemical analysis of the groundwater showed that the mean concentration of the cations was in the order: Na+ > Ca2+ > Mg2+ > K+, while that for anions was SO3 2− > Cl > HCO3  > NO3 . The most prevalent water type is Na–SO4 followed by water types Na–Cl and Ca–SO4. The chemical evolution of groundwater is primarily controlled by water–rock interactions: mainly weathering of aluminosilicates, dissolution of sulfate minerals, and cation exchange reactions. Sulfate dissolution and pyrite weathering may both contribute to the SO4 2− load of the groundwater. High Na+ concentrations in groundwater participate in ion-exchange processes, resulting in the displacement of base cations into solution and raised concentrations in groundwater. The principal component analysis (PCA) performed on groundwater identified three principal components controlling variability of groundwater chemistry. Electrical conductivity, Ca2+, Mg2+, Na+, SO4 2−, and Cl content were associated in the same component (PC1) (salinity), most likely linked to anthropogenic activities.  相似文献   

15.
Stable hydrogen and oxygen isotope has important implication on water and moisture transportation tracing research. Based on stable hydrogen (δD) and oxygen (δ18O) isotope using a Picarro L1102-i and water chemistry (e.g. major ions, pH, EC and TDS) measurement, this study discussed the temporal variation and characteristics of stable hydrogen and oxygen isotope, chemistry (e.g. TDS, pH, EC, Ca2+, Mg2+, Na+ and Cl-) in various water bodies including glacier meltwater runoff, ice and snow, and precipitation at the Laohugou glacier basin during June 2012 to September 2013. Results showed that δD and δ18O in the meltwater runoff varied obviously with the temporal change from June to September, showing firstly increasing trend and then decreasing trend, with the highest values in July with high air temperature and strong glacier melting, which could indicate the temporal change of glacier melting process and extent. Variations of δD and δ18O in the runoff were similar with that of snow and ice on the glacier, and the values were also above the GMWL, which probably implied that the glacier runoff was mainly originated from glacier melting and precipitation supply. The glacier meltwater chemical type at the Laohugou glacier basin were mainly composed by Ca-Na-HCO3-SO4 and Ca-Mg-HCO3-SO4, which also varied evidently with the glacier melting process in summer. By analyzing the temporal change of stable hydrogen and oxygen isotope and chemistry in the melting period, we find it is easy to separate the components of the snow and ice, atmospheric precipitation and melt-runoff in the river, which could reflect the change process of glacier melting during the melting period, and thus this work can contribute to the glacier runoff change study of large-scale region by stable isotope and geochemical method in future.  相似文献   

16.
Aerosol samples were collected in the Shiyi Glacier,Qilian Mountains from July 24 to August 19,2012 and analyzed for major water-soluble ionic species(F-,Cl-,NO2-,NO3-,SO42-,Na+,NH4+,K+,Mg2+ and Ca2+) by ion chromatography. SO42- and NH4+ were the most abundant components of all the anions and cations,with average concentrations of 94.72 and 54.26 neq/m3,respectively,accounting for 34% and 20% of the total water-soluble ions analyzed.These mean ion concentrations were generally comparable with the background conditions in remote sites of the Qilian Mountains,but were much lower than those in certain cities in China.The particles were grouped into two dominant types according to their morphology and EDX signal:Si-rich particles and Fe-rich particles.Backward air mass trajectory analysis suggested that inland cities may contribute some anthropogenic pollution to this glacier,while the arid and semi-arid regions of central Asia were the primary sources of the mineral particles.  相似文献   

17.
This paper reports on hydrochemical features of diluted waters in the source areas and the brine end-members dominant in the playa of the Salinas Grandes Basin, Córdoba, Argentina. Special emphasis was placed on the study of the relationship between geomorphology and the resulting hydrochemical fractionation. Inflow is from springs and mountain streams which disappear before reaching the saline complex. The playa and intermittent saline lakes are mainly fed by groundwater flow and a few moderately saline and perennial springs. Conversely, ephemeral lakes are fed by atmospheric precipitation and groundwater, whereas small ponds are only fed by atmospheric precipitation. The absence of a clear linkage between geomorphological units and water types was evident in the source areas. Up to four types of water were recognized in a given geomorphological unit. From the sandflat downward towards the playa, the correspondence between geomorphological units and water types was clear, coinciding with a decreased hydrochemical heterogeneity. In this subenvironment, I have recognized two dominant types of water (SO 4 2– –Cl–HCO 3 –Na+ and Cl–SO 4 2– –HCO 3 –Na+), which can be considered the original members of the neutral brine in the playa (Cl–SO 4 2– –Na+ where Ca2++Mg2+ do not surpass 5 meq per cent), and an intermediate type in the mudflat (Cl–SO 4 2– –Na+ where the contribution of Ca2++Mg2+ reaches up to 15 meq per cent). It seems evident that in the zone between the source areas and the sandflat, hydrochemistry is governed by chemical weathering. In stream floodplains and in the distal alluvial plain, close to the saline complex, the increase in water types as well as the increase of HCO 3 with respect to SO 4 2– , were explained by the mixture of aquifers controlled by the Salinas Grandes-Salinas de Ambargasta fracture. In the saline complex, the more concentrated end-members are the result of evaporation of the two more frequent water-types in the sandflat subenvironment, and salt dissolution of ancient evaporite deposit.  相似文献   

18.
Effect of water quality on the leaching of potassium from sandy soil   总被引:1,自引:0,他引:1  
When potassium (K+) fertilizers are applied to soil, K+ is subject to displacement through the soil profile. More generally, the application of K+ fertilizers to sandy soils with low clay content and small buffer capacity, in which K+ does not interact strongly with the soil matrix, results in localized increases in K+ concentration in the soil solution. Losses of K+ depend on the concentration of calcium (Ca2+) as a competing ion in the leaching water and the amount of water that passes through the soil. In this study, we examined the adsorption and movement of applied K+ in columns of sandy soil. Glass tubes, 4.8 cm in diameter and 40 cm in length, were packed with either native soil or Ca2+-saturated soil. The resulting 10-cm-long column of soil had a bulk density of 1.65 g cm−3. Native soil was leached with distilled water and CaCl2 solutions of various concentrations. In the Ca2+-saturated soil, a pulse of K+ was leached with CaCl2 solutions of various concentrations or distilled water. Increasing the CaCl2 concentration from 3 to 15 mm resulted in earlier breakthrough, a higher peak concentration of K+, and greater amounts of leached K+. The breakthrough curve for K+, when leached with distilled water, showed very low concentrations and was more delayed than the other treatments. In Ca2+-saturated soil, the amount of K+ leached increased as Ca2+ concentration increased, with up to 54% of the added pulse K+ being removed from 10 pore volumes (Pv) (387 mm) of 15 mm CaCl2. The presence of Ca2+ in irrigation water and soil minerals able to release Ca2+ is important in determining the amount of K+ leached from soils. Large amounts of K+ are leached from soils in areas where crops are irrigated with water that contains significant concentrations of Ca2+ and other cations.  相似文献   

19.
引入湖泊经纬度、海拔、湖水温度、湖水pH值以及湖水Na+、K+、Mg2+、Ca2+、Cl-、SO2-4、CO2-3、HCO-3浓度等13个基本变量作为聚类指标,构建了自组织特征映射(SOFM)网络,对巴丹吉林沙漠南部共计105个常年积水湖泊进行了非线性聚类,并与基于类平均法的线性聚类分析结果作对比,得到两种聚类分析方法的结果大体一致,即以雅布赖山北东—南西走向断裂带为界,湖泊呈较明显的二聚类分布,断裂带北部的湖泊聚集一类,接近断裂带以及断裂带南部的湖泊聚为一类,这与实地考察结果相互印证。对聚类结果进行判别后发现,SOFM网络的聚类结果更为准确可靠,其在识别地理现象微小差异方面更具优势。而根据断裂带两侧不同类型湖泊的分布,可以推断巴丹吉林沙漠南部湖泊群地下水源补给空间上的非同源性,以及地下岩层组分和结构上的空间差异性。  相似文献   

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