首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 37 毫秒
1.
In recent years, a series of important progresses have been made in the aspect of magnesium isotopes behavior in weathering processes. These progresses are not only favorable to understand the change of the magnesium isotopic compositions in rivers, but also establish the foundation to further reveal the magnesium isotope geochemical cycle. The magnesium in rivers is both magnesium sink for weathering and magnesium source for the ocean. The Mg isotopic compositions in rivers are dominated by the magnesium sources and Mg isotope fractionations processes. The sources of magnesium in rivers originate mainly from draining rocks, as well as less contribution from the eolian deposition, groundwater, plant debris, and precipitation. The Mg isotope fractionations in rivers are mainly related to precipitation and dissolution of carbonate minerals, silicate mineral hydrolysis, adsorption on mineral or colloidal matter surface, and plant uptake. Generally, the contribution of carbonate minerals dissolution or precipitation is equal to add or reduce magnesium from carbonate endmember, which has a remarkably negative δ26Mg value. Based on the fact that most clay minerals are rich in 26Mg during nature silicate mineral hydrolysis, then it is possible to infer that residual weathering products enrich in 26Mg. However, there is no significant Mg isotope fractionation causing by the adsorption on mineral or colloidal matter surface during river water migration. For the plant uptake, the root prefers to have 26Mg, leading the plant itself rich in heavier Mg isotopic composition. In addition, formation of secondary minerals in rivers could also reflect the changes of chemical parameters in rivers (such as major elements, CO2 solubility, pH, etc.). Hence, Mg isotopic composition in rivers and associated isotope fractionations are not only the basis for the application of magnesium isotope to trace surface material cycle, but also have important significance for the further understanding the geochemical cycle of magnesium isotopes.  相似文献   

2.
  相似文献   

3.
The aim of this work is to evaluate the hydrogeochemical characteristics of groundwater in parts of the lower Benue Through in Nigeria as well as to evaluate the variation in groundwater chemistry data and the suitability of the groundwater for drinking and other domestic purposes. This was based on chemical analyses of 44 water samples from existing wells and boreholes in the study area. From the statistical analysis (wide ranges, median and standard deviation), it is obvious that there are significant variations in the quality/composition of groundwater in the period of sampling. The calculated SAR, Na% and RSC values indicated that the water is of excellent to good quality and is suitable for irrigation. Na and HCO3 are dominant with respect to the chemical composition of the groundwater. On the basis of water chemistry, hydrochemical indices and factor analysis the dominant controls or processes affecting the distribution of geochemical variables in the study area have been shown to be water/rock interaction which is mainly controlled by carbonate and silicate dissolution as well as anthropogenic influence to a lesser extent. Additional processes include cation exchange reactions and reverse ion exchange to a minor extent.  相似文献   

4.
吴初  武雄  钱程  朱阁 《现代地质》2017,31(3):629
对内蒙古杭锦旗气田区浅层地下水运用Piper三线图、Gibbs图、氯碱指数图等方法进行水化学特征及其形成作用分析研究,结果表明：杭锦旗气田区浅层地下水具有较高的矿化度,偏碱性,硬度较大,枯水期TDS浓度和总硬度高于丰水期;研究区浅层地下水化学组分在小范围内具有一定的空间变异性,地下水阳离子以Na+、Ca2+为主,阴离子以HCO3-为主,水化学类型主要有HCO3 Ca型、HCO3 Na型和SO4·Cl Na型;研究区浅层地下水化学组分来源于碳酸盐矿物、硅铝酸盐矿物和蒸发岩的风化溶解,且丰水期和枯水期水化学组分有微弱变化,地下水化学特征的形成以岩石风化溶解作用为主。  相似文献   

5.
广汉市平原区浅层地下水化学演化及其控制因素   总被引：4，自引：0，他引：4  
为在广汉市城乡规划过程中提供地下水资源开发利用的基础信息,采用矿物风化系统分析、相关性分析、主成分分析和PhreeQC反向水文地球化学模拟等方法对广汉市平原区的浅层地下水的地下水水化学组分进行分析,确定了浅层地下水的水化学演化及控制因素,完成了地下水资源的质量及时空分布特征分析。分析表明：Gibbs图显示岩石风化主导该区地下水水化学特征,风化过程产生离子和次生矿物又经历水解作用,在矿物风化系统稳定场图中显示水样中铝硅酸盐矿物逐渐趋于溶解,碳酸盐矿物处于饱和状态;PhreeQC反向水文地球化学模拟结果显示在水流模拟路径上主要发生了钙蒙脱石、钾长石溶解和高岭石、石英、钠长石的沉淀,以及Ca-Na2之间的阳离子交换吸附作用;离子相关性和主成分分析进一步的验证了溶滤作用、蒸发浓缩作用和阳离子交换吸附作用是引起浅层地下水水化学过程和矿物组成改变的主要原因。研究区地下水水质总体不会对人体健康造成不良影响。  相似文献   

6.
Rapid population growth, industrialization, and agricultural expansion in the Khoy area (northwestern Iran) have led to its dependence on groundwater and degradation of groundwater quality. This study attempts to decipher the major processes and factors that degrade the groundwater quality of the Khoy plain. For this purpose, 54 groundwater samples from unconfined and confined aquifers of the plain were collected in July 2017 and analyzed for major cations and anions (Na, K, Ca, Mg, HCO3, SO4, and Cl), minor ions (NO3 and F), and Al. Magnesium and bicarbonate were identified as the dominant cation and anion, respectively. Several ionic ratios and geochemical modeling using PHREEQC indicated that the most important hydrogeochemical processes to affect groundwater quality in the plain were weathering and dissolution of evaporitic and silicate minerals, mixing, and ion exchange. There were smaller effects from evaporation and anthropogenic factors (e.g., industries). Results showed that the high salinity of the groundwater in the northeast area of the plain was due to the high solubility of the evaporitic minerals, e.g., halite and gypsum. Reverse ion exchange and the contribution of mineral dissolution were more significant than ion exchange in the northeastern part of the plain. Elevated salinity of the groundwater in the southeast was attributed mostly to reverse ion exchange and somewhat to evaporation.  相似文献   

7.
Evaluation of major ion chemistry and solute acquisition process controlling water chemical composition were studied by collecting a total of fifty-one groundwater samples in shallow (<25 m) and deep aquifer (>25 m) in the Varanasi area. Hydrochemical facies, Mg-HCO3 dominated in the largest part of shallow groundwater followed by Na-HCO3 and Ca-HCO3 whereas Ca-HCO3 is dominated in deep groundwater followed by Mg-HCO3 and Na-HCO3. High As concentration (>50 μg/l) is found in some of the villages situated in northeastern parts (i.e. adjacent to the concave part of the meandering Ganga river) of the Varanasi area. Arsenic contamination is confined mostly in tube wells (hand pump) within the Holocene newer alluvium deposits, whereas older alluvial aquifers are having arsenic free groundwater. Geochemical modeling using WATEQ4F enabled prediction of saturation state of minerals and indicated dissolution and precipitation reactions occurring in groundwater. Majority of shallow and deep groundwater samples of the study area are oversaturated with carbonate bearing minerals and under-saturated with respect to sulfur and amorphous silica bearing minerals. Sluggish hydraulic conductivity in shallow aquifer results in higher mineralization of groundwater than in deep aquifer. But the major processes in deep aquifer are leakage of shallow aquifer followed by dominant ion-exchange and weathering of silicate minerals.  相似文献   

8.
北京平原区永定河冲洪积扇地下水水化学特征与演化规律   总被引：4，自引：0，他引：4  
本文以北京市平原区永定河冲洪积扇地下水化学场的演化机理及地下水水循环规律为研究目的,根据水化学特征的水平分布及典型剖面上的演化过程研究,得到以下结论:1)从永定河冲洪积扇顶部补给区到扇缘排泄区,地下水水化学类型呈现水平分带性,潜水水化学类型由Ca-HCO3过渡到Ca·Mg-HCO3、Mg·Na-SO4,局部因人类活动影...  相似文献   

9.
The study area Mettur forms an important industrial town situated NW of Salem district. The geology of the area is mainly composed of Archean crystalline metamorphic complexes. To identify the major process activated for controlling the groundwater chemistry an attempt has been made by collecting a total of 46 groundwater samples for two different seasons, viz., pre-monsoon and post-monsoon. The groundwater chemistry is dominated by silicate weathering and (Na + Mg) and (Cl + SO4) accounts of about 90% of cations and anions. The contribution of (Ca + Mg) and (Na + K) to total cations and HCO3 indicates the domination of silicate weathering as major sources for cations. The plot for Na to Cl indicates higher Cl in both seasons, derived from Anthropogenic (human) sources from fertilizer, road salt, human and animal waste, and industrial applications, minor representations of Na also indicates source from weathering of silicate-bearing minerals. The plot for Na/Cl to EC indicates Na released from silicate weathering process which is also supported by higher HCO3 values in both the seasons. Ion exchange process is also activated in the study area which is indicated by shifting to right in plot for Ca + Mg to SO4 + HCO3. The plot of Na-Cl to Ca + Mg-HCO3-SO4 confirms that Ca, Mg and Na concentrations in groundwater are derived from aquifer materials. Thermodynamic plot indicates that groundwater is in equilibrium with kaolinite, muscovite and chlorite minerals. Saturation index of silicate and carbonate minerals indicate oversaturation during pre-monsoon and undersaturation during post-monsoon, conforming dissolution and dilution process. In general, water chemistry is guided by complex weathering process, ion exchange along with influence of Cl ions from anthropogenic impact.  相似文献   

10.

The relevance of groundwater hydrogeochemistry to explain the occurrence and distribution of arsenic in groundwater is of great interest. The insightful discussions on the control of shallow groundwater (< 50 m) hydrogeochemistry in arsenic mobilization are known to be a viable tool to explain the arsenic menace in shallow groundwater. The present investigation emphasizes the hydrogeochemical driver and/or control over the reductive dissolution of Fe-bearing host minerals and thereby releasing arsenic into the shallow groundwater of the study area. The study suggests that hydrogeochemical evolution is mainly governed by carbonate minerals dissolution, silicate weathering, and competitive ion-exchange processes in the shallow aquifers (< 50 m). The present study also indicates the prevalence of carbonate minerals dissolution over silicate weathering. The emergence of Cl− concentration in the shallow groundwater founds the possibilities of anthropogenic inputs into the shallow aquifers (< 50 m). The reducing environment in shallow aquifers (< 50 m) of the study area is evident in the reductive dissolution of Fe- bearing shallow aquifer minerals which absorb arsenic in the solid phase and mobilize arsenic onto shallow groundwater. The study opted for many statistical approaches to delineate the correlation among major and minor ionic constituents of the groundwater which are very helpful to understand the comprehensive mechanism of arsenic mobilization into shallow groundwater.

  相似文献   

11.
Douala city, located in the littoral province of Cameroon, receives abundant rainfall quantities due to its geographical position in the Gulf of Guinea and bears considerable surface water and groundwater resources. Due to socioeconomic development and rapid demographic growth in the city and its consequences of unplanned urbanization and improper sanitation system, these water resources are poorly protected and managed. Streams in the Wouri watershed receive large amounts of wastewater discharge, and hundreds of boreholes have been drilled into the aquifer system without any management plan. A detailed hydrodynamic and hydrogeochemistry study in Douala town and its environs was conducted to get a better insight into the groundwater system functioning in order to provide information for the sustainable management and protection of the groundwater resource. Two field campaigns were carried out with 187 samples collected and analyzed for major ions, stable isotopes (18O, 2H), and tritium 3H. The results of the sampling have shown that the weathering of silicate minerals is the dominant geochemical process affecting groundwater chemistry in this system. However, acid rainfall in the humid climate has also caused carbonate mineral dissolution, amorphous silica deposition, and ion exchange reactions to occur in aquifers in the region. The various water types identified were categorized into four major clusters C1 to C4, based on the major ion composition and the local hydrogeological conditions. Environmental isotope data reveal that modern-to-submodern waters occur in the phreatic Quaternary/Mio-Pliocene and Oligocene/Upper Eocene aquifers, respectively. These results corroborate with the conceptual model built where modern groundwater types indicated silicate mineral weathering and calcite dissolution (C1 and C2), whereas submodern groundwater mostly showed silica deposition, ion exchange, and, to a lesser extent, carbonate mineral dissolution (C3 and C4). This improved understanding of the aquifer system functioning is essential to provide a reasonable basis for effective control measures and sustainable water management.  相似文献   

12.
Surface water samples were collected from Langtang Lirung glacier outlet point to the Narayani river system in central Nepal in order to investigate the role of elevation in the variation of chemistry along the drainage networks. The chemistry of Langtang–Narayani river system was dominated by sulfide oxidation coupled with carbonate dissolution and weathering of silicate minerals. Calcium and magnesium concentrations were relatively higher than other cations and the sum of both species strongly correlated with alkalinity, supporting the dissolution of carbonate and dolomite as the dominant source for these ions. Aluminosilicate minerals primarily as albite and anorthite appeared as dominant silicate minerals within the drainage basin. Bisiallitization was the dominant type of weathering within the entire drainage system. Hydrogen ion concentration was lower in the low elevation sites than in high elevation sites reflecting the more consumption of carbon dioxide in the low elevation sites due to enhanced chemical weathering rates. Furthermore, major solutes like sum of base cations, silicon as well as alkalinity increased in concentration in the lower elevation sites. All regulating factors appeared to be directly related to elevation and hence elevation appeared to be the prime factor for the variation in chemical species along the Langtang–Narayani river system. Toshiyuki Masuzawa: deceased.  相似文献   

13.
柳林泉域滞流区岩溶水的热源及其Na+、Cl-来源探讨   总被引：1，自引：1，他引：0  
柳林泉域滞流区岩溶水以高温、高Na+和Cl-浓度为主要特征。文章在区域地质及水文地质条件分析基础上,采用化学计量学原理,判断了该区岩溶水的热源及Na+和Cl-的来源。结果显示:在泉域的补给区、径流区和排泄区的上青龙、龙门会、杨家港和寨东泉组,岩溶水中的Na+和Cl-主要来源于岩盐的溶解,其中多余的Na+可能来自于阳离子交换、黄土中含Na+矿物的溶解及城市污水的排放;滞流区和排泄区的刘家疙瘩泉组岩溶水中高浓度的Na+和Cl-也主要来自于岩盐的溶解,而多余的Cl-可能由岩溶水中的Na+交换吸附介质中的Ca2+或Mg2+所致。西部滞流区岩溶水的热源主要包括地温梯度增热、当地正常地温、岩石中放射性元素产热和石膏的溶解放热,其贡献率分别为45%、28%、20%和7%。   相似文献   

14.
The Sanzhao depression and Qijia-gulong depression are two of the most important hydrocarbon-bearing sub-depressions in the Songliao basin, dominated by Cretaceous fluvial and lacustrine strata with volcanic and volcaniclastic rocks. In this paper, the pressure distributions and hydrochemistry variations in those two depressions are investigated. It is found that the Qijia-gulong depression is dominated by overpressure, but the Sanzhao depression is dominated by underpressure, especially in the Quantou formation. The salinity of formation water ranges from 1.0 g/L to 20 g/L, with a mean of 4 g/L in most formations. Water composition is dominated by NaHCO3 water type but varies greatly in salinity and ionic ratios in the different depressions. The results of mass balance calculation reveal that, fluid chemistry in the Qijia-gulong depression is dominated by dissolution of silicate minerals and halite, whereas in the Sanzhao depression it is dominated by silicate mineral dissolution, evaporite dissolution (halite and gypsum), carbonate mineral dissolution/precipitation, and cation exchange.  相似文献   

15.
The flooding of the abandoned iron mines of Lorraine leads to a degradation of the groundwater quality. Laboratory experiments allowed us to build a kinetic chemical model based on simple chemical mechanisms. During mining operations, pyrite oxidation and carbonate dissolution lead to the precipitation of gypsum. The local decrease of pH favours local dissolutions of minerals and releases ions that are fixed on cationic exchange sites. During the flooding of the mine workings, the dissolution of the newly precipitated gypsum, the precipitation of carbonates and cationic exchange reactions are responsible for the increase of the concentrations of sulphate, magnesium, sodium, potassium and strontium in water. Thereafter, these concentrations would decrease with the natural leaching of the mining reservoir. To cite this article: P. Collon et al., C. R. Geoscience 336 (2004).  相似文献   

16.
西藏是我国重要的生态安全屏障,拉萨地区地下水化学特征及形成机制研究,对揭示青藏高原现代表生过程变化机理具有重要作用,对服务国家生态安全建设具有重要意义。本文通过拉萨地区地下水调查、水样采集与分析,综合运用Gibbs模型模拟、水化学分析方法分析了地下水化学特征及水岩作用机理。结果表明:地下水电导率介于38.801 193.00 μS/cm,平均值为123.99 μS/cm,总溶解性固体(total dissolved solids,TDS)含量介于44.051 050.55 mg/L,平均值为150.75 mg/L,pH值大于7,属弱碱性水,地下水化学类型为HCO3-Ca型和Cl-Na型,其中Cl-Na型水为地下温泉水。地下水形成过程主要是碳酸盐岩和硅酸盐岩的溶解、阳离子交换等作用下的结果,且受到一定程度的人为因素影响;地下水中的Na+、K+和Cl-主要来自盐岩矿物的风化溶解,过量的Na+、K+来源于钠长石和钾长石等硅酸盐矿物的溶解, HCO 3 -、Ca2+、Mg2+和 SO 4 2 -主要来自方解石、白云石、石膏以及其他含钙镁矿物的溶解。  相似文献   

17.
高东东  吴勇  王春红 《地下水》2010,32(6):49-53,132
彭州地区是＂5.12＂地震灾区,其震后的水文地球化学特征还未有相关研究,本文利用以热力学为基础的水文地球化学平衡理论与方法对彭州通济地区震后浅层地下水化学特征及其形成进行了分析,为研究地震对浅层地下水的影响提供基础信息。分析表明：研究区水化学场受到地形地貌的控制,水化学类型以HCO3--Ca型为主;HCO3-、Ca2＋普遍含量较高,CO2分压控制碳酸盐的溶解度及水中的pH值;其浅层地下水相对于石英处于过饱和状态,相对于非晶质SiO2处于未饱和状态,CO2气体参与硅酸盐矿物水解,产生可溶SiO2;矿物溶解及与水中化学组分平衡的非硅铝酸盐矿物主要为方解石,硅铝酸盐矿物主要为长石,其次是高岭石、蒙脱石。水化学平衡理论与方法可以较好的用于研究地下水所处的水文地球化学环境以及判断SiO2的来源和矿物溶解过程。  相似文献   

18.
Hydrogeochemistry of groundwater is important for sustainable development and effective management of the groundwater resource. Fifty-six groundwater samples were collected from shallow tube wells of the intensively cultivated southern part of district Bathinda of Punjab, India, during pre- and post-monsoon seasons. Conventional graphical plots were used to define the geochemical evaluation of aquifer system based on the ionic constituents, water types, hydrochemical facies and factors controlling groundwater quality. Negative values of chloroalkaline indices suggest the prevalence of reverse ion exchange process irrespective of the seasons. A significant effect of monsoon is observed in terms chemical facies as a considerable amount of area with temporary hardness of Ca2+–Mg2+–HCO3 ? type in the pre-monsoon switched to Ca2+–Mg2+–Cl? type (18%) followed by Na+–HCO3 ? type (14%) in the post-monsoon. Evaporation is the major geochemical process controlling the chemistry of groundwater process in pre-monsoon; however, in post-monsoon ion exchange reaction dominates over evaporation. Carbonate weathering is the major hydrogeochemical process operating in this part of the district, irrespective of the season. The abundance of Ca2+ + Mg2+ in groundwater of Bathinda can be attributed mainly to gypsum and carbonate weathering. Silicate weathering also occurs in a few samples in the post-monsoon in addition to the carbonate dissolution. Water chemistry is deteriorated by land-use activities, especially irrigation return flow and synthetic fertilisers (urea, gypsum, etc.) as indicted by concentrations of nitrate, sulphate and chlorides. Overall, results indicate that different natural hydrogeochemical processes such as simple dissolution, mixing, weathering of carbonate minerals locally known as ‘‘kankar’’ and silicate weathering are the key factors in both seasons.  相似文献   

19.
This study aims to investigate the hydrochemical characteristics of shallow aquifer in a semi-arid region situated in northwest Algeria, and to understand the major factors governing groundwater quality. The study area is suffering from recurring droughts, groundwater resource over-exploitation and groundwater quality degradation. The approach used is a combination of traditional hydrochemical analysis methods of multivariate statistical techniques, principal component analysis (PCA), and ratios of major ions, based on the data derived from 33 groundwater samples collected in February 2014. Results show that groundwater in the study area are highly mineralized and collectively has a high concentration of chloride (as Cl?). The dominant water types are Na-Cl (27%), Mg-HCO3 (24%) and Mg-Cl (24%). According to the (PCA) approach, salinization is the main process that controls the hydrochemical variability. The PCA analysis reveal the impact of anthropogenic factor especially the agricultural activities on the groundwater quality. The PCA highlighted two types of recharge: Superficial recharge from effective rainfall and excess irrigation water distinguished by the presence of nitrate and lateral recharge or vertical leakage from carbonate formations marked by the omnipresence of HCO3?. Additionally, three categories of samples were identified: (1) samples characterized by good water quality and receiving notable recharge from carbonate formations; (2) samples impacted by the natural salinization process; and (3) samples contaminated by anthropogenic activities. The major natural processes influencing water chemistry are the weathering of carbonate and silicate rocks, dissolution of evaporite as halite, evaporation and cation exchange. The study results can provide the basis for local decision makers to ensure the sustainable management of groundwater and the safety of drinking water.  相似文献   

20.
张建忙  范冠宇  王琦 《江苏地质》2023,47(3):322-329
为系统掌握南通海门区浅层地下水水化学现状,在采集区域地下水样本并分析水化学特征的基础上,综合运用描述性统计、相关性分析、Piper三线图、Gibbs模型以及离子比例系数法等分析手段,对南通海门区浅层地下水化学特征及其形成机理进行系统分析。结果表明：HCO3-和Ca2+分别是研究区浅层地下水中占比最大的阴、阳离子;HCO3-Ca和HCO3-Ca·Mg型为该地区主要地下水化学类型;浅层地下水TDS和总硬度的平均质量浓度相对较低,平均值分别为598.00、374.32 mg/L。根据相关性分析,Cl-和Mg2+为影响该区域地下水TDS的特征因子。研究区浅层地下水化学特征主要受到岩石风化作用影响,地下水水质成分主要源自碳酸盐岩和硅酸盐岩等的长期风化溶解。同时,逆向阳离子交换作用也在一定程度上影响着浅层地下水化学的组成。研究结果可为该区地下水开发利用管理提供理论依据和数据支撑。  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号