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 31 毫秒
1.
Seasonal variation of ground water in Nayagarh district, Odisha is determined by analysing both pre and post monsoon water samples. The high fluoride content is an endemic problem in the area and special attention was attached to the point. The chemical compositions of the ground water of the area are dominated by CaCl, NaCl and mixed CaMgCl types in pre-monsoon and CaHCO3-mixed CaMgCl type in post-monsoon. This is largely due to chemical weathering of Eastern Ghats Mobile Belt rock types. Increasing alkalinity vis-a-vis F concentration in pre-monsoon is associated with sodium-bicarbonate water types having high pH (>7) and low calcium and magnesium contents. The percentage of total high fluoride containing water samples is nearly double in pre-monsoon than in post-monsoon. During both the seasons, pH values indicate mildly alkaline to weakly acidic nature of the water samples. Fluoride concentration has good correlation with pH in pre-monsoon whereas in post-monsoon it shows good correlation with Fe. Facies analysis indicates that water is becoming predominantly Ca-Na cation and Cl-SO4-HCO3 anion type in premonsoon than Ca-Mg type and HCO3-Cl-SO4 type in post-monsoon. The seasonal variations in concentrations of anthropogenic components demonstrate that the groundwater system is very less liable to pollution by human activities.  相似文献   

2.
The chemical characteristics of surface, groundwater and mine water of the upper catchment of the Damodar River basin were studied to evaluate the major ion chemistry, geochemical processes controlling water composition and suitability of water for domestic, industrial and irrigation uses. Water samples from ponds, lakes, rivers, reservoirs and groundwater were collected and analysed for pH, EC, TDS, F, Cl, HCO3, SO4, NO3, Ca, Mg, Na and K. In general, Ca, Na, Mg, HCO3 and Cl dominate, except in samples from mining areas which have higher concentration of SO4. Water chemistry of the area reflects continental weathering, aided by mining and other anthropogenic impacts. Limiting groundwater use for domestic purposes are contents of TDS, F, Cl, SO4, NO3 and TH that exceed the desirable limits in water collected from mining and urban areas. The calculated values of SAR, RSC and %Na indicate good to permissible use of water for irrigation. High salinity, %Na, Mg-hazard and RSC values at some sites limit use for agricultural purposes.  相似文献   

3.
Prior to mining, the water in and around the mine is rarely influenced by human activities, and hydrogeochemical processes are the major factors influencing and controlling water chemistry. To identify these natural hydrogeochemical processes in Laoheba phosphorite mine (Sichuan Province, China), correlation and multivariate statistical techniques were used. Results show that water quality in the area is generally good before the Laoheba phosphorite mine goes into construction and production. The cluster analysis classified water samples into 4 clusters (C1–C4). Samples from C1 and C2 are of HCO3?Ca·Mg and HCO3?Ca type, while those from C3 and C4 are of HCO3?Ca·Mg type. Most parameters except Cl? and pH show an increasing trend in the order of C1 to C4. Three principal components were extracted, and PC1 represents the ion exchange and the weathering of calcite, dolomite, and silicate minerals. PC2 and PC3 indicate the process of water recharge from upstream waters and the process of evaporation, respectively. The hydrochemistry of waters in the area is a result of multiple factors, and natural mineral weathering and ion exchange are the most important ones.  相似文献   

4.
 The lower Vamsadhara river basin, spreading over an area of 817 sq.km in northern Andhra Pradesh, represents a typical rural setting. The occurrence of phosphorus-bearing minerals reported in literature, and the increasing application of phosphatic fertilizers in the area have prompted these studies. Water samples from 113 wells were analysed for Ca, Mg, Na, K, Cl, SO4, HCO3, F, NO3 and PO4. The results indicate the presence of phosphate in the groundwater ranged from 0.72 to 7.07 mg/l, which is beyond the limits recommended for domestic and water treatment purposes. Samples of soils and weathered rocks were analyzed for their water-soluble phosphate and other chemical parameters. The water-soluble phosphate in the widely used fertilizers of the area was determined. The spatial variation of phosphate in the aquifer and the soil leachate characteristics supplemented by the chemical equilibrium calculations clearly indicate the dominance of geological sources over the fertilizer sources in contributing PO4 to the groundwaters. Received: 4 March 1996 / Accepted: 29 July 1996  相似文献   

5.
An attempt has been made to study the groundwater geochemistry in part of the NOIDA metropolitan city and assessing the hydrogeochemical processes controlling the water composition and its suitability for drinking and irrigation uses. The analytical results show that Na and Ca are the major cations and HCO3 and Cl are the major anions in this water. The higher ratios of Na+K/TZ+ (0.2–0.7), Ca+Mg/HCO3 (0.8–6.1); good correlation between Ca-Mg (0.75), Ca-Na (0.77), Mg-Na (0.96); low ratio of Ca+Mg/Na+K (1.6), Ca/Na (1.03), Mg/Na (0.64), HCO3/Na (1.05) along with negative correlation of HCO3 with Ca and Mg signify silicate weathering with limited contribution from carbonate dissolution. The hydro-geochemical study of the area reveals that many parameters are exceeding the desirable limits and quality of the potable water has deteriorated to a large extent at many sites. High concentrations of TDS, Na, Cl, SO4, Fe, Mn, Pb and Ni indicate anthropogenic impact on groundwater quality and demand regional water quality investigation and integrated water management strategy. SAR, %Na, PI and Mg-hazard values show that water is of good to permissible quality and can be used for irrigation. However, higher salinity and boron concentration restrict its suitability for irrigation uses at many sites.  相似文献   

6.
Ayadi  Rahma  Trabelsi  Rim  Zouari  Kamel  Saibi  Hakim  Itoi  Ryuichi  Khanfir  Hafedh 《Hydrogeology Journal》2018,26(4):983-1007

Major element concentrations and stable (δ18O and δ2H) and radiogenic (3H and 14C) isotopes in groundwater have proved useful tracers for understanding the geochemical processes that control groundwater mineralization and for identifying recharge sources in the semi-arid region of Sfax (southeastern Tunisia). Major-ion chemical data indicate that the origins of the salinity in the groundwater are the water–rock interactions, mainly the dissolution of evaporitic minerals, as well as the cation exchange with clay minerals. The δ18O and δ2H relationships suggest variations in groundwater recharge mechanisms. Strong evaporation during recharge with limited rapid water infiltration is evident in the groundwater of the intermediate aquifer. The mixing with old groundwater in some areas explains the low stable isotope values of some groundwater samples. Groundwaters from the intermediate aquifer are classified into two main water types: Ca-Na-SO4 and Ca-Na-Cl-SO4. The high nitrate concentrations suggest an anthropogenic source of nitrogen contamination caused by intensive agricultural activities in the area. The stable isotopic signatures reveal three water groups: non-evaporated waters that indicate recharge by recent infiltrated water; evaporated waters that are characterized by relatively enriched δ18O and δ2H contents; and mixed groundwater (old/recent) or ancient groundwater, characterized by their depleted isotopic composition. Tritium data support the existence of recent limited recharge; however, other low tritium values are indicative of pre-nuclear recharge and/or mixing between pre-nuclear and contemporaneous recharge. The carbon-14 activities indicate that the groundwaters were mostly recharged under different climatic conditions during the cooler periods of the late Pleistocene and Holocene.

  相似文献   

7.
Overextraction of groundwater is widely occurring along the coast where good quality groundwater is at risk, due to urbanization, tourist development and intensive agriculture. The Sabratah area at the northern central part of Jifarah Plain, Northwest Libya, is a typical area where the contamination of the aquifer in the form of saltwater intrusion, gypsum/anhydrite dissolution and high nitrate concentrations is very developed. Fifty groundwater samples were collected from the study area and analysed for certain parameters that indicate salinization and pollution of the aquifer. The results demonstrate high values of the parameters electrical conductivity, sodium, potassium, magnesium, chloride and sulphate which can be attributed to seawater intrusion. The intensive extraction of groundwater from the aquifer reduces freshwater outflow to the sea, creates drawdown cones and lowering of the water table to as much as 30 m below mean sea level. Irrigation with nitrogen fertilizers and domestic sewage and movement of contaminants in areas of high hydraulic gradients within the drawdown cones probably are responsible for the high nitrate concentration towards the south of the region. Seawater intrusion and deep salt water upconing result in general high SO4 2? concentrations in groundwater near the shoreline, where localized SO4 2? anomalies are also due to the dissolution of sebkha deposits for few wells in the nearby sebkhas. Upstream, the increase in SO4 2? concentrations in the south is ascribed to the dissolution of gypsum at depth in the upper aquifer.  相似文献   

8.
文章对纳米比亚欢乐谷地区白岗岩型铀矿床流体包裹体的温度、盐度、密度和成分等进行了系统的分析研究,厘定了成矿流体的类型及基本性质,并对该地区铀成矿的物理化学条件和成矿流体来源进行了初步探讨。研究表明,该地区白岗岩型铀矿床的成矿流体可分为2个期次:主成矿期和叠加改造期。主成矿期的流体为岩浆晚期的残余高温、低盐度热液,其气相成分主要是CO2,含少量H2O、N2和CH4;叠加改造期的流体为中-低温、低盐度热液,其气相成分以CO2和H2O为主,含少量CH4和N2,来源于岩浆期后热液与大气水的混合。  相似文献   

9.
《Applied Geochemistry》2001,16(7-8):745-758
The physical–chemical characteristics of the groundwater in the Baza–Caniles detrital aquifer system indicate that a wide diversity of hydrochemical conditions exists in this semiarid region, defining geochemical zones with distinct groundwater types. The least mineralized water is found closest to the main recharge zones, and the salinity of the water increases significantly with depth towards the center of the basin. Geochemical reaction models have been constructed using water chemistry data along flow paths that characterize the different sectors of the aquifer system, namely: Quaternary aquifer, unconfined sector and shallow and deep confined sectors of the Mio–Pliocene aquifer. Geochemical mass–balance calculations indicate that the dominant groundwater reaction throughout the detrital system is dedolomitisation (dolomite dissolution and calcite precipitation driven by gypsum dissolution); this process is highly developed in the central part of the basin due to the abundance of evaporites. Apart from this process, there are others which influence the geochemical zoning of the system. In the Quaternary aquifer, which behaves as a system open to gases and which receives inputs of CO2 gas derived from the intensive farming in the area, the interaction of the CO2 with the carbonate matrix of the aquifer produces an increase in the alkalinity of the water. In the shallow confined sector of the Mio–Pliocene aquifer, the process of dedolomitisation evolves in a system closed to CO2 gas. Ca2+/Na+ cation exchange and halite dissolution processes are locally important, which gives rise to a relatively saline water. Finally, in the deep confined sector, a strongly reducing environment exists, in which the presence of H2S and NH+4 in the highly mineralized groundwater can be detected. In this geochemical zone, the groundwater system is considered to be closed to CO2 gas proceeding from external sources, but open to CO2 from oxidation of organic matter. The geochemical modeling indicates that the chemical characteristics of this saline water are mainly due to SO4 dissolution, dedolomitisation and SO4 reduction, coupled with microbial degradation of lignite.  相似文献   

10.
The Vea catchment, mainly underlain by crystalline basement rocks, is located in Northern Ghana. Hydrogeochemical studies were carried out in this area with the objective of identifying the geochemical processes influencing water quality and suitability of surface and groundwater for agricultural and domestic uses. Sixty-one groundwater and four surface water samples were collected from boreholes, dams and rivers and analysed for Ca2+, Mg2+, Na+, K+, HCO3 ?, Cl?, and SO4 2?, Fetot, PO4 3?, Mntot, NH4 +, NO3 ?, NO2 ?. In addition, pH, total dissolved solids, electrical conductivity, total hardness, turbidity, colour, salinity and dissolved oxygen were analysed. Chloro-alkaline indices 1 and 2, and characterization of weathering processes suggest that the chemistry of groundwater is dominated by the interaction between water and rocks. Cation exchange and silicate weathering are the dominant processes controlling the chemical composition of the groundwater in the area studied. Mineral saturation indices indicate the presence of at least three groups of groundwater in the Vea catchment with respect to residence time. The meteoric genesis index suggests that 86% of the water samples belong to the shallow meteoric water percolation type. The findings further suggest that the groundwater and surface water in the basin studied are mainly Ca–Mg–HCO3 water type, regardless of the geology. Compared to the water quality guidelines of WHO, the study results on sodium absorption ratio, sodium percentage, magnesium hazard, permeability index and residual sodium carbonate indicate that groundwater and surface water in the Vea catchment are generally suitable for drinking and irrigation purposes.  相似文献   

11.
In the light of progressive depletion of groundwater reservoir and water quality deterioration of the Neyveli basin, an investigation on dissolved major constituents in 25 groundwater samples was performed. The main objective was detection of processes for the geochemical assessment throughout the area. Neyveli aquifer is intensively inhabited during the last decenniums, leading to expansion of the residential and agricultural area. Besides semi-aridity, rapid social and economic development stimulates greater demand for water, which is gradually fulfilled by groundwater extraction. Groundwaters of the study area are characterized by the dominance of Na?+?K over Ca?+?Mg. HCO3 was found to be the dominant anion followed by Cl and SO4. High positive correlation was obtained among the following ions: Ca–Mg, Cl–Ca,Mg, Na–K, HCO3–H4SiO4, and F–K. The hydrochemical types in the area can be divided into two major groups: the first group includes mixed Ca–Mg–Cl and Ca–Cl types. The second group comprises mixed Ca–Na–HCO3 and Ca–HCO3 types. Most of the groundwater samples are within the permissible limit of WHO standard. Interpretation of data suggests that weathering, ion exchange reactions, and evaporation to some extent are the dominant factors that determine the major ionic composition in the study area.  相似文献   

12.
Studies of groundwater chemistry in the Koilsagar project area of Andhra Pradesh indicate that the waters are sodium bicarbonate, sodium chloride, mixed cationic-mixed anionic, mixed cationic Na dominating bicarbonate, and mixed cationic Ca dominating bicarbonate types. Of them, sodium bicarbonate and mixed cationic Mg dominating bicarbonate types of waters are more prevalent.Isocone mapping of specific conductance indicates that the ionic concentration increases from east to west in the area. Graphical treatment of chemical data reveals that, in general, the area has basic water, whereas the left flank canal area is dominated by secondary alkaline water, and Pallamarri and Pedda Rajmur villages have strongly acidic waters. Ion-exchange studies show that cation-anion exchanges exist all over the area except for two places, which have a base exchange hardened type of water.Graphical representation further shows that most of the area has medium salinity-low sodium (C2S1) water useful for irrigation purposes. High salinity-low sodium (C3S1) and high salinity-medium sodium (C3S2) waters are present in some areas, which need adequate drainage to overcome the salinity problem.  相似文献   

13.
Environmental geochemistry of Damodar River basin, east coast of India   总被引：1，自引：0，他引：1  
 Water and bed sediment samples collected from the Damodar River and its tributaries were analysed to study elemental chemistry and suspended load characteristics of the river basin. Na and Ca are the dominant cations and HCO3 is the dominant anion. The water chemistry of the Damodar River basin strongly reflects the dominance of continental weathering aided by atmospheric and anthropogenic activities in the catchment area. High concentrations of SO4 and PO4 at some sites indicate the mining and anthropogenic impact on water quality. The high concentration of dissolved silica, relatively high (Na+K)/TZ+ ratio (0.2–0.4) and low equivalent ratio of (Ca+Mg)/(Na+K) indicate that dissolved ions contribute significantly to the weathering of aluminosilicate minerals of crystalline rocks. The seasonal data show a minimum ionic concentration in the monsoon season, reflecting the influence of atmospheric precipitation on total dissolved solids contents. The suspended sediments show a positive correlation with discharge and both discharge and suspended load reach their maximum value during the monsoon season. Kaolinite is the mineral that is possibly in equilibrium with the water. This implies that the chemistry of the Damodar River water favours kaolinite formation. The concentration of heavy metals in the finer size fraction (<37 μ m) is significantly higher than the bulk composition. The geoaccumulation index values calculated for Fe, Mn, Zn, Ni and Cr are well below zero, suggesting that there is no pollution from these metals in Damodar River sediments. Received: 21 January 1998 · Accepted: 4 May 1998  相似文献   

14.
《Applied Geochemistry》2003,18(7):1043-1063
The Memphis aquifer in southwestern Tennessee is confined to a semi-confined unconsolidated sand aquifer and is the primary municipal water source in the Memphis metropolitan area. Past studies have identified regions in the metropolitan area in which the overlying upper Claiborne confining unit lacks significant clay and provides a hydraulic connection between the shallow aquifer and the Memphis aquifer. In this study, major solute chemistry, 3H, and 3H/3He groundwater dating are used to investigate the extent and chemical effects of leakage through the confining unit to the Memphis aquifer in the vicinity of a municipal well field. The 3H/3He dates and geochemical modeling of the chemical data are used to constrain mixing fractions and the timing of modern recharge. Tritium activities of as much as 2.8 TU are observed in shallow production wells, but deeper production wells have 3H activities that approach the detection limit. Trends in water chemistry indicate vertical mixing in the aquifer of shallow Na–SO4–Cl-rich water and deeper Ca–Mg–HCO3-rich water. Water chemistry does not vary consistently with seasonal pumping, but 3H activity generally decreases during low use periods. Stable O and H isotopes show little variation and are not useful groundwater tracers for this study. The 3H-bearing, Na–SO4–Cl-rich water is interpreted to reflect recharge of modern water through the upper Claiborne confining unit. The 3H/3He dates from 5 production wells indicate modern recharge, that infiltrated 15–20 a ago, is present in the shallow production wells. Geologic data and hydrologic boundary conditions suggest that the most likely source for continued leakage is a nearby stream, Nonconnah Creek. Geochemical reaction modeling using the NETPATH computer code suggests that proportions of shallow aquifer water leaking into the Memphis aquifer range from 6 to 32%. The 3H/3He dating and NETPATH modeling results correlate well, suggesting that these complementary analytical tools provide an effective means to evaluate proportions of modern water leaking into semi-confined aquifers. These results also indicate a need to carefully consider connections between surface water and semi-confined groundwater resources in wellhead protection programs.  相似文献   

15.
To investigate the applicability of equilibrium modeling for the estimation of the chemical changes of acid mine waters, the phases predicted to precipitate by equilibrium calculation were compared with what actually precipitates from the stream and acid mine waters in the Dogyae area, Korea. The computer program MINTEQA2 was used for the equilibrium calculations based on the chemical compositional data of the water samples collected in the study area. XRD, IR, thermal and chemical analyses of the collected precipitates were performed to identify their phases.The results of the identification of the collected precipitates are inconsistent with what the equilibrium calculations predict. The equilibrium calculations indicate that ferrihydrite, FeOHSO4, gibbsite, and AlOHSO4 should precipitate from the stream and acid mine waters in the study area. However, the experimental analyses show that only ferrihydrite and Al4(OH)10SO4 are the recognizable precipitates on the bottom of the stream and mine drainage channels. Comparing the stability relations among the possible precipitates with the field occurrence of the precipitates in the study area suggests that FeOHSO4 and AIOHSO4 are kinetically inhibited to precipitate and metastable ferrihydrite and Al4(OH)10SO4 appear in their stability field instead. It indicates that the chemical compositional change of the waters due to the solid phase precipitation in the study area must be interpreted and predicted in terms of the precipitation of not the phases predicted by the equilibrium calculation but the actually identified ones.Assuming that the dissolved species in the aqueous phase are in equilibrium with respect to the currently precipitating solid phases in the study area, the water chemistries are attempted to interpret based on the plot of the theoretically calculated activities of the dissolved species on the stability diagram for the identified precipitates and gibbsite. The plot reveals a few evolution paths of the chemical composition of the acid mine water as the acid generation and neutralization progress. The evolution path producing ferrihydrite and then Al4(OH)10SO4 precipitation suggests that the system including acid producing pyrite has lost significant amounts of its neutralizing capacity and thus, become intolerable to the impacts from acid mine water.  相似文献   

16.
The study area, the Fasa Plain, is situated in the semiarid region of Fars Province in the south of Iran. The Salloo diapir is a salt dome that crops out in the northwest of the study area. Isotopic and hydrochemical analyses were used to examine the water and how the origin of salinity and the diapir affect the quality of the groundwater quality in the study area. Groundwater was sampled from 31 representative pumping wells in alluvial aquifer and five springs in order to measure their stable isotope compositions, bromide ion concentration, and physical and chemical parameters. The alluvial aquifer was organized into two main groups based on the chemistry, with Group 1 consisting of low-salinity well samples (544–1744 µS/cm) with water type Ca–Mg–HCO3–SO4 which were taken in the center and north of the area, and Group 2 consisting of high-salinity samples (2550–4620 µS/cm) with water type Ca–Mg–Cl–SO4 which were taken from the wells in the south and southwest of the area. A saline spring near the salt dome with an EC of 10,280 µS/cm has water type Na–Cl, while the compositions of the water in the other karstic springs is comparable to the fresh groundwater samples. All groundwater samples are undersaturated with respect to gypsum, anhydrite, and halite and are supersaturated with respect to calcite and dolomite. Stable isotopes (δ18O and δ2H) differentiated four water types: saline springs, freshwater spring, fresh groundwater, and saline groundwater. The results indicate that meteoric water is the main origin of these water resources. Halite dissolution from the salt dome was identified as the origin of salinity. The Na/Cl and Cl/Br ratios confirmed the results. Groundwater compositions in the southwestern part of the area are affected by the intrusion of saltwater from the salt dome. The average saltwater fraction in the some water wells is about 0.2%. In the south and southwestern part of the area, the saltwater fraction is positive in mixed freshwater/saltwater (Group 2). Different processes interact together to change the hydrochemical properties of Fasa’s alluvial aquifer. The main processes that occur in the aquifer are mixing, gypsum dissolution, and calcite precipitation.  相似文献   

17.
Nitrate contamination in irrigation groundwater,Isfahan, Iran   总被引：1，自引：1，他引：0  
Groundwater is one of the major sources of water in Isfahan. Efficient management of these resources requires a good understanding of its status. This paper focuses on the hydrochemistry and also it wants to assess the nitrate concentration in irrigation groundwater of Isfahan suburb. All the groundwater samples are grouped into three categories, including Na-Cl + Ca-Cl (63 %), Na-SO4 + Ca-SO4 (23 %) and Ca-HCO3 (14 %). According to the EC and SAR, the most dominant classes are C3S1, C4S2 and C4S3. 55 % of samples indicate very high salinity and medium to very high alkalinity that is not suitable for irrigation. 84 % of the groundwater samples show nitrate contents higher than HAV (13 mg l?), while more than 25 % exceeded the maximum contamination level (44.27 mg l?) according to EPA regulations. The horizontal and vertical distribution patterns of nitrate in groundwater samples show a surficial origin for nitrate contamination. The high nitrate content can be attributed to the agricultural activities along with domestic sewage and industrial wastewaters in populated area. Based on results, using high nitrate groundwater for irrigation can minimize the requirement for inorganic fertilizers and reduce the cost of cultivation and nitrate contamination.  相似文献   

18.
河北汤泉地热流体水文地球化学特征及其成因   总被引：7，自引：5，他引：2       下载免费PDF全文
提要：汤泉位于河北省遵化市西北部,为山前丘陵地貌,地热资源丰富。本文通过对该地区地热流体研究发现：Na+、Ca2+、K+、Mg2+与SO2-4、HCO-3、Cl-、NO-3是该地区地下热水的主要成分,水化学类型主要为SO2-4-Na+型,属于未污染的天然弱碱性水;流体中F-含量平均为9.36 mg/l,远高于国家地下水质量标准ⅴ级;可溶性SiO2的含量可作为地热温标;地热流体总矿化度平均为782.33 mg/l,属于淡水;为中等腐蚀型水,不结碳酸钙垢,无CaSO4?2H2O垢和SiO2垢生成的可能;地热流体属于含岩盐地层溶滤的陆相沉积水;根据氢氧稳定同位素可知,河北汤泉地热流体主要来源于大气降水。  相似文献   

19.
李状  苏晶文  董长春  叶永红  杨洋 《中国地质》2022,49(5):1509-1526
【研究目的】 了解长江中下游平原地区地下水流系统并深入分析其地下水水化学特征及其演化机制。【研究方法】 综合马鞍山市当涂地区的水文地质条件、水动力场等,基于研究区水化学基本特征,运用多元统计分析、水化学图件、离子比值和反向水文地球化学模拟等方法对该地区浅层地下水水化学演化进行分析。【研究结果】 结果表明：（1）研究区地下水主要为低矿化度偏碱性水,地下水组分中阳离子以Ca2+和Mg2+为主,阴离子以HCO3-和SO42-为主。（2）研究区地下水水化学类型主要可分为7类,其中松散岩类孔隙含水岩组和碎屑岩类孔隙裂隙含水岩组的水化学类型主要为HCO3-Ca型、HCO3-Ca·Na型、HCO3·Cl-Ca·Na型以及HCO3-Ca·Mg型;基岩类裂隙含水岩组的化学类型主要为HCO3·SO4-Ca·Mg型和SO4·HCO3-Ca·Mg型。（3）研究区浅层地下水水样超标率为46%,总体水质较差,超标率较高的组分依次为Mn、高锰酸盐指数（CODMn）、硝酸盐（以N计）、Fe、As、氨氮（以N计）等。（4）研究区地下水的化学组分主要受到岩石风化作用的控制;此外,还存在Na-Ca的正向阳离子交替吸附作用。反向水文地球化学模拟结果进一步定量论证了水岩相互作用对本区浅层地下水组分的形成和演化起着主导作用。【结论】 研究区地下水主要为低矿化度偏碱性,主要可分为松散岩类孔隙水、碎屑岩类孔隙裂隙水和基岩类裂隙水。主要离子比例和反向水文地球化学模拟揭示了本区浅层地下水化学组分主要是地下水溶滤方解石、白云石等碳酸盐矿物、石英、长石等硅酸盐矿物,高岭土等黏土矿物以及岩盐、石膏等达到过饱和之后形成的。  相似文献   

20.
Natural and anthropogenic impacts on karst ground water, Zunyi, Southwest China, are discussed using the stable isotope composition of dissolved inorganic carbon and particulate organic carbon, together with carbon species contents and water chemistry. The waters can be mainly characterized as HCO3–Ca type, HCO3 · SO4–Ca type, or HCO3 · SO4–Ca · Mg type, according to mass balance considerations. It is found that the average δ13CDIC values of ground waters are higher in winter (low-flow season) than in summer (high-flow season). Lower contents of dissolved inorganic carbon (DIC) and lower values of δ13CDIC in summer than in winter, indicate that local rain events in summer and a longer residence time of water in winter play an important role in the evolution of ground water carbon in karst flow systems; therefore, soil CO2 makes a larger contribution to the DIC in summer than in winter. The range of δ13CDIC values indicate that dissolved inorganic carbon is mainly controlled by the rate of carbonate dissolution. The concentrations of dissolved organic carbon and particulate organic carbon in most ground water samples are lower than 2.0 mg C L−1 and 0.5 mg C L−1, respectively, but some waters have slightly higher contents of organic carbon. The waters with high organic carbon contents are generally located in the urban area where lower δ13CDIC values suggest that urbanization has had an effect on the ground water biogeochemistry and might threaten the water quality.  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