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1.
Groundwater with high salinity is widespread in different climatic and geologic environments of the world. The formation of its chemical composition, however, is still debatable. The chemical composition of groundwater has been studied in 19 springs of the Tuva depression. In this area, hydrocarbonate, sulfate, and chloride waters with different cation compositions discharge. Their TDS value varies mainly from 1 to 6 g/L, reaching 315 g/L at only one locality. The chemical composition of the studied waters is reflective of the geostructural, hydrogeologic, landscape, and geochemical conditions. The main processes determining the chemical composition of the waters are their interaction with aluminosilicate minerals, dissolution of gypsum and halite, evaporation, and oxidation of sulfide minerals.  相似文献   

2.
《Applied Geochemistry》2004,19(8):1233-1254
Combined hydrogeological and hydrogeochemical data allow flow systems and the origins of solutes in the Honeysuckle Creek area of the southeastern Murray Basin, which is an area affected by dryland salinity, to be constrained. Recharge occurs both on the uplands that are composed of fractured Violet Town Volcanic rocks and the Riverine Plain that comprises sediments of the Shepparton and Coonambidgal Formations. Groundwater from the Violet Town Volcanics has low salinity (<20 mmol/L Cl) and major ion geochemistry that is controlled largely by dissolution of silicate minerals. Low Cl/Br ratios (as low as 281 molar) suggest that this groundwater has not dissolved halite. Groundwater that recharged through the Riverine Plain sediments has higher Cl/Br ratios (up to 1146) and Cl concentrations of <20 mmol/L, consistent with it dissolving minor halite. Higher salinity (>20 mmol/L) groundwater has intermediate Cl/Br ratios (600–1000), which indicate that the high salinities do not simply result from halite dissolution. Rather, mixing of groundwater homogenises Cl/Br ratios, and evaporation as a consequence of a shallow water table is the dominant process that increases salinity. Oxygen and H isotopes also indicate that mixing and evaporation have occurred. These results indicate that land use over the whole region, not just the uplands, needs to be considered in any salinity management plans. Additionally future development of salinity is controlled by depth to the water table on the plains and the efficiency of recharge rather than by salt stores (halite or brines) in the unsaturated zone.  相似文献   

3.
河套灌区西部浅层地下水咸化机制   总被引：2，自引：0，他引：2       下载免费PDF全文
浅层地下水水位埋深浅、含盐量高,是导致河套灌区土壤次生盐渍化的重要原因.以河套灌区西部地区为研究区,通过对浅层地下水的水化学和氢氧同位素特征分析以及水文地球化学模拟,探讨了灌区浅层地下水的补给来源和主控水-岩作用过程,并定量估算了蒸发作用对浅层地下水含盐量的影响.研究区内浅层地下水为弱碱性咸水,pH为7.23~8.45,总溶解性固体（total dissolved solids,TDS）变化范围为371~7 599 mg/L;随着地下水咸化程度增大,水化学类型由HCO3-Na·Mg·Ca型向Cl-Na型过渡.引黄灌溉和大气降水是浅层地下水的主要补给来源,径流过程中浅层地下水受蒸发作用和植物蒸腾作用影响,地下水化学组分主要来源于蒸发盐溶解和硅酸盐风化水解,并受强烈的蒸发作用和离子交换作用影响.水文地球化学模拟和主成分分析结果显示,蒸发作用和岩盐溶解作用对区内浅层地下水咸化贡献最大,石膏和白云石等矿物的溶解、硅酸盐的水解、Na-Ca离子交换以及局部地形起伏对地下水咸化过程也有较大贡献.   相似文献   

4.
《Applied Geochemistry》2004,19(5):645-664
Sediment and water samples from 12 saline pans on the semi-arid west coast of South Africa were analysed to determine the origin of salts and geochemical evolution of water in the pans. Pans in the area can be subdivided into large, gypsiferous coastal pans with 79–150 g/kg total dissolved salt (TDS), small inland brackish to saline (2–64 g/kg TDS) pans and small inland brine (168-531 g/kg TDS) pans that have a layer of black sulphidic mud below a halite crust. The salinity of coastal pan waters varies with the seasonal influx of dilute runoff and dissolution of relict Pleistocene marine evaporite deposits. In contrast, inland pans are local topographic depressions, bordered on the north by downslope lunette dunes, where solutes are concentrated by evaporation of runoff, throughflow and groundwater seepage. The composition of runoff and seepage inflow waters is determined by modification of coastal rainfall by weathering, calcite precipitation and ion exchange reactions in the predominantly granitic catchment soils. Evaporation of pan waters leads to precipitation of calcite, Mg–calcite, dolomite, gypsum and halite in a distinct stratigraphic succession in pan sediments. Bicarbonate limits carbonate precipitation, Ca limits gypsum precipitation and Na limits halite precipitation. Dolomitisation of calcite is enhanced by the high Mg/Ca ratio of brine pan waters. Brine pan waters evolve seasonally from Na–Cl dominated brines in the wet winter months to Mg–Cl dominated brines in the dry summer months, when 5–20 cm thick halite crusts cover pan surfaces. Pan formation was probably initiated during a drier climate period in the early Holocene. More recent replacement of natural vegetation by cultivated land may have accelerated salt accumulation in the pans.  相似文献   

5.
This paper reveals the geochemical processes of dissolution, precipitation and cation exchange that took place during water–rock interaction between water seepages through the Tannur Dam. The Schoeller diagram indicates that there are three major water types originating during water–rock interaction. The first water type is characterized by low salinity that ranges from 1,300 to 2,800 µs/cm, which represents the reservoir water and the water in the right side of the central gallery. The second water type is in the left side of the central gallery, which exhibits medium salinity that reaches about 4,400 µs/cm. The third water type is characterized by very high salinity that reaches a value of around 8,500 µs/cm and represents the water in the right existing adit. The increase of salinity can be explained due to the dissolution of carbonate and sulfate minerals that form the matrix of the foundation and the abutment rocks, and the dissolution of the grout curtain, which is composed of cement and bentonite. Hydrogeochemical modeling, using a computer code PHREEQC, was used to obtain the saturation indices of specific mineral phases, which might be related to interaction with water seepages, and to identify the chemical species of the dissolved ions. The thermodynamic calculations indicate that most of the water samples were undersaturated with respect to gypsum, anhydrite and halite, and were saturated and/or supersaturated with respect to calcite and dolomite. Ca(HCO3)2 is the primary water type, as a result of dissolution of carbonate minerals such as calcite and dolomite prevailing at the dam site. However, cation-exchange processes are responsible for the formation of the Na2SO4 water type from the CaSO4 type that formed due to the dissolution of gypsum.  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.
Major ion and stable isotope geochemistry allow groundwater/surface-water interaction associated with saline to hypersaline lakes from the Willaura region of Australia to be understood. Ephemeral lakes lie above the water table and locally contain saline water (total dissolved solids, TDS, contents up to 119,000 mg/L). Saline lakes that lack halite crusts and which have Cl/Br ratios similar to local surface water and groundwater are throughflow lakes with high relative rates of groundwater outflows. Permanent hypersaline lakes contain brines with TDS contents of up to 280,000 mg/L and low Cl/Br ratios due to the formation of halite in evaporite crusts. These lakes are throughflow lakes with relatively low throughflow rates relative to evaporation or terminal discharge lakes. Variations in stable isotope and major ion geochemistry show that the hypersaline lakes undergo seasonal cycles of mineral dissolution and precipitation driven by the influx of surface water and evaporation. Despite the generation of highly saline brines in these lakes, leakage from the adjacent ephemeral lakes or saline throughflow lakes that lack evaporite crusts is mainly responsible for the high salinity of shallow groundwater in this region.  相似文献   

8.
陈中红  查明 《地质科学》2010,45(2):476-489
东营凹陷古近系水化学场分布与湖盆演化有着良好的对应关系,矿化度从深到浅逐渐降低,体现出沉积环境开放性的增强。高矿化度分布是咸化湖盆重要特征,盐岩溶解、扩散、运移和断裂沟通是其主要成因。在这种高矿化度地层水化学场中主要发育CaCl_2水型,在盆地边缘低矿化度地层水中,以NaHCO_3水型为主,同时发育有少量低—较高矿化度的Na_2SO_4水型和MgCl_2水型。对东营凹陷大量实测地层水及油气性质资料分析表明:东营凹陷CaCl_2水型指示地层封闭性条件较好的还原环境,在该环境中油气藏分布最为广泛,目前发现的高矿化度(100 g/L)油藏与CaCl_2水型相关;低矿化度(10 g/L)NaHCO_3水型指示封闭性条件差、水交替强烈的水文流畅环境,对油气聚集不利,可形成次生油气藏;高矿化度(30～100g/L)的NaHCO_3水型对油气聚集也有利,在该水型中多形成原生油气藏,其成因与地幔高浓度的CO_2运移及断裂通道的沟通作用有关;研究区高矿化度(30 g/L)Na_2SO_4水型的形成与膏盐有关,其中可形成原生油气藏;低矿化度Na_2SO_4水型指示封闭性条件差的氧化环境,对油气聚集不利。研究结果表明,在东营凹陷断陷咸化湖盆中,含NaHCO_3水型的地层环境更能代表地层水交替强烈的开放性沉积环境,而Na_2SO_4水型分布多与硫酸盐有关;东营凹陷表现出高矿化度的NaHCO_3水型和Na_2SO_4水型等异常地层水环境,但在各类型地层水环境中油气藏都有所发现,显示出典型断陷咸化湖盆中水化学场分布特征及与油气成藏之间独特的相互关系。  相似文献   

9.
The data on the mineral composition and crystallization conditions of magnesian skarn and magnetite ore at contacts of dolerite with rock salt and dolomite in ore-bearing volcanic—tectonic structures of the Angara—Ilim type have been integrated and systematized. Optical microscopy, scanning and transmission electron microscopy, electron microprobe analysis, electron paramagnetic resonance, Raman and IR spectroscopy, and methods of mineralogical thermometry were used for studying minerals and inclusions contained therein. The most diverse products of metasomatic reactions are found in the vicinity of a shallow-seated magma chamber that was formed in Lower Cambrian carbonate and saliferous rocks under a screen of terrigenous sequences. Conformable lodes of spinel-forsterite skarn and calciphyre impregnated with magnesian magnetite replaced dolomite near the central magma conduit and apical portions of igneous bodies. At the postmagmatic stage, the following mineral assemblages were formed at contacts of dolerite with dolomite: (1) spinel + fassaite + forsterite + magnetite (T = 820?740°C), (2) phlogopite + titanite + pargasite + magnetite (T = 600–500°C), And (3) clinochlore + serpentine + pyrrhotite (T = 450°C and lower). Rock salt is transformed at the contact into halitite as an analogue of calciphyre. The specific features of sedimentary, contact-metasomatic, and hydrothermal generations of halite have been established. The primary sedimentary halite contains solid inclusions of sylvite, carnallite, anhydrite, polyhalite, quartz, astrakhanite, and antarcticite; nitrogen, methane, and complex hydrocarbons have been detected in gas inclusions; and the liquid inclusions are largely aqueous, with local hydrocarbon films. The contact-metasomatic halite is distinguished by a fine-grained structure and the occurrence of anhydrous salt phases (CaCl2 · KCl, CaCl2, nMgCl2 · mCaCl2) and high-density gases (CO2, H2S, N2, CH4, etc.) as inclusions. The low-temperature hydrothermal halite, which occurs in skarnified and unaltered silicate rocks and in ore, is characterized by a low salinity of aqueous inclusions and the absence of solid inclusions. The composition and aggregative state of inclusions in halite and forsterite indicate that salt melt-solution as a product of melting and dissolution of salt was the main agent of high-temperature metasomatism. Its total salinity was not lower than 60%. The composition and microstructure of magnetite systematically change in different mineral assemblages. Magnetite is formed as a result of extraction of iron together with silicon and phosphorus from dolerite. The first generation of magnetite is represented by mixed crystals, products of exsolution in the Fe-Mg-Al-Ti-Mn-O system. The Ti content is higher at the contact of dolerite with rock salt, whereas, at the contact with dolomite, magnetite is enriched in Mg. The second generation of magnetite does not contain structural admixtures. The distribution of boron minerals and complex crystal hydrates shows that connate water of sedimentary rocks could have participated in hydrothermal metasomatic processes.  相似文献   

10.
Emerald mineralisation in Colombia is located in two distinct zones along the borders of the Eastern Cordillera, some 80 km apart. Mineralisation in the western zone has been dated at ca. 35 Ma whereas in the eastern zone it is 30 Ma older. Crush leach analysis of the electrolyte chemistry of fluid inclusions contained in emerald, quartz, calcite, dolomite and fluorite from both zones, demonstrates that in each region brines associated with emerald mineralisation range between two extremes with many samples yielding intermediate compositions. Fluid 1, found mainly in emerald-hosted fluid inclusions, is dominated by NaCl with high Cl:Br ratios indicating that the salinity was derived by dissolution of halite, most probably from the local salt beds. Fluid 2, found notably in quartz hosted-fluid inclusions, is of similar salinity but contains less Na and significant concentrations of Ca–K–Fe–Cl and other cations. It has lower Cl:Br ratios, more comparable with formation waters, but is inferred to have obtained part of its salinity by halite dissolution. Bivariate plots of almost all cations have linear or sublinear trends regardless of the mineral hosting the inclusions or the locality from which the samples originated, demonstrating that mixing of the two saline fluids has occurred. Because the same two fluids occur in both eastern and western zones, despite the difference in space and time, it is inferred that fluid compositions were rock controlled by similar interactions with evaporites and black shales in both instances. It is proposed that beryllium was transported as Be–F complexes in the NaCl-fluid, and was precipitated as emerald after mixing with the calcic brine caused precipitation of fluorite and parisite. Received: 9 April 1999 / Accepted: 14 March 2000  相似文献   

11.
The aim is to define the mechanism of chemical reactions that are responsible for the salinization of the Azraq basin along groundwater flow path, using inverse modeling technique by PHREEQC Interactive 2.8 for Windows. The chemical analysis of representative groundwater samples was used to predict the causes of salinization of groundwater. In addition, the saturation indices analysis was used to characterize the geochemical processes that led to the dissolution of mineral constituents within the groundwater aquifer system. According to the modeling results, it was noted that the groundwater at the recharge area was undersaturated with respect to calcite, dolomite, gypsum, anhydrite, and halite. Thus, the water dissolved these minerals during water rock interaction, and therefore, the concentration of Ca, Mg, Na, and SO4 increased along the groundwater flow path. Furthermore, the groundwater at the discharge area was oversaturated with respect to calcite and dolomite. This meant that the water would precipitate these minerals along the flow path, while the water was undersaturated with respect to gypsum and halite throughout the simulated path; this showed the dissolution processes that take place during water-rock interaction. Therefore, the salinity of the groundwater increased significantly along the groundwater flow paths.  相似文献   

12.
Geochemistry of soil, soil water, and soil gas was characterized in representative soil profiles of three Michigan watersheds. Because of differences in source regions, parent materials in the Upper Peninsula of Michigan (the Tahquamenon watershed) contain only silicates, while those in the Lower Peninsula (the Cheboygan and the Huron watersheds) have significant mixtures of silicate and carbonate minerals. These differences in soil mineralogy and climate conditions permit us to examine controls on carbonate and silicate mineral weathering rates and to better define the importance of silicate versus carbonate dissolution in the early stage of soil-water cation acquisition.Soil waters of the Tahquamenon watershed are the most dilute; solutes reflect amphibole and plagioclase dissolution along with significant contributions from atmospheric precipitation sources. Soil waters in the Cheboygan and the Huron watersheds begin their evolution as relatively dilute solutions dominated by silicate weathering in shallow carbonate-free soil horizons. Here, silicate dissolution is rapid and reaction rates dominantly are controlled by mineral abundances. In the deeper soil horizons, silicate dissolution slows down and soil-water chemistry is dominated by calcite and dolomite weathering, where solutions reach equilibrium with carbonate minerals within the soil profile. Thus, carbonate weathering intensities are dominantly controlled by annual precipitation, temperature and soil pCO2. Results of a conceptual model support these field observations, implying that dolomite and calcite are dissolving at a similar rate, and further dissolution of more soluble dolomite after calcite equilibrium produces higher dissolved inorganic carbon concentrations and a Mg2+/Ca2+ ratio of 0.4.Mass balance calculations show that overall, silicate minerals and atmospheric inputs generally contribute <10% of Ca2+ and Mg2+ in natural waters. Dolomite dissolution appears to be a major process, rivaling calcite dissolution as a control on divalent cation and inorganic carbon contents of soil waters. Furthermore, the fraction of Mg2+ derived from silicate mineral weathering is much smaller than most of the values previously estimated from riverine chemistry.  相似文献   

13.
The Barwon Downs Graben lies on the northern flanks of the Otway Ranges and is situated approximately 70 km southwest of Geelong, Victoria, Australia. The major lower Tertiary Barwon Downs Graben aquifer comprises highly permeable sands and gravels interbedded with clays and silts of the hydraulically interconnected Pebble Point, Dilwyn and Mepunga Formations. Groundwater flows east into the Barwon Downs Graben from the Barongarook High, and yields 14C ages up to ～20 ka implying that recharge rates are low and, consequently, that the resource could be impacted by overabstraction. The presence of three different lithological units has led to the development of localized flow systems that has resulted in a lack of regular spatial variations in groundwater chemistry. Stable isotopic data suggests that groundwater was recharged under similar climatic conditions as of today. The major ion chemistry of the freshest groundwater is dominated by Na and HCO3 while higher TDS groundwater, from the confining Narrawaturk Marl, is dominated by Na and Cl. Cl/Br ratios are close to rainfall suggesting that halite dissolution is not the principle source of salts. An excess of Na relative to Cl in fresher groundwater suggests that feldspar dissolution has occurred, however, water–rock interaction is limited. The concentrations of Ca, Mg, and SO4 are controlled by silicate dissolution and ion-exchange reactions with clays.  相似文献   

14.
In Wadi Tharad the groundwater has been subjected to hydrochemical study to identify the process (s) that led to the formation of relatively highly saline water in shallow alluvial aquifer. The chemical analyses results show that the groundwater salinity was highly variable and randomly distributed along the wadi course. This variation could be attributed to intensive evaporation on effluent prone surface irrigation water that led to precipitation of evaporates (e.g., calcite, dolomite, gypsum and probably halite). The intensive irrigation practice through mineral dissolution recharged the groundwater with a marked increase in the salinity. The local hydrogeological condition is also involved in determining the risk of the groundwater salinity as a consequence of irrigation practice. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

15.
Konarsiah salt diapir is situated in the Simply Folded Zone of the Zagros Mountain, south Iran. Eight small permanent brine springs emerge from the Konarsiah salt body, with average total dissolved solids of 326.7 g/L. There are numerous brackish to saline springs emerging from the alluvial and karst aquifers adjacent to the diapir. Concerning emergence of Konarsiah diapir in the study area, halite dissolution is the most probable source of salinity in the adjacent aquifers. However, other sources including evaporation and deep brines through deep Mangerak Fault are possible. The water samples of the study area were classified based on their water-type, salinity, and the trend of the ions concentration curves. The result of this classification is in agreement with the hydrogeological setting of the study area. The hydrochemical and isotopic evaluations show that the groundwater samples are the result of mixing of four end members; Gachsaran sulfate water, Sarvak and Asmari carbonate fresh waters, and diapir brine. The molar ratios of Na/Cl, Li/Cl, Br/Cl, and SO4/Cl; and isotopic signature of the mixed samples justify a groundwater mixing model for the aquifers adjacent to the salt diapir. The share of brine in each adjacent aquifer was calculated using Cl mass balance. In addition, concentrations of 34 trace elements were determined to characterize the diapir brine and to identify the possible tracers of salinity sources in the mixed water samples. B, Mn, Rb, Sr, Cs, Tl, and Te were identified as trace elements evidencing contact of groundwater with the salt diapir.  相似文献   

16.
Thermal and mineral waters in north-eastern Slovenia   总被引：2，自引：0，他引：2  
 The Mura basin in north-eastern Slovenia is made up of two depressions, developed during the Late Neogene and Early Pliocene all within a widespread system of Pannonian basins. Both depressions are characterized by the occurrence of thermal waters of somewhat different hydrogeochemical character. Radgona depression is in the northern part of the basin and reaches depths of about 2 km. Thermal waters are generally dominated by sodium-bicarbonate, not related to the age of an aquifer, its wallrock composition, the type of porosity or total concentration of dissolved solids. Locally, sulphate-rich waters are encountered, and they are related to the presence of gypsum in the rocks of pre-Tertiary basement. The adjacent Ljutomer depression is over 4 km deep and comprises compartments with stagnant or semi-stagnant aquifers. Herein saline waters predominate, even in the aquifers of carbonate composition and abundant CO2 gas. In shallower, unconsolidated, intergranular aquifers sodium-bicarbonate waters predominate. Thermal aquifers of this type are very important to the economy of the region, but they are also subjected to overexploitation which is reflected in time-dependent changes of dynamic pressures, temperature, conductance, salinity, pH and concentration of major ions, trace elements, dissolved gasses, and total organic carbon. Mineral waters occur in shallow aquifers or springs in marginal areas of the Radgona depression. Bicarbonate waters are dominated by calcium, or both calcium and sodium. Some mineral waters are formed mainly by penetration of CO2 gas into shallow aquifers and consequent water–rock interaction. Composition of some mineral waters indicate their possible evolution from thermal waters which have risen from central parts of the Radgona depression along deep-seated faults, and have been modified by cooling and mixing processes. Received: 30 November 1998 · Accepted: 22 March 1999  相似文献   

17.
《Applied Geochemistry》2004,19(9):1355-1365
Hydrogeochemical assessment of 40 saline waters and brines from 20 locations within the lower (southern) and middle regions of the Benue-Trough, Nigeria are presented and discussed in terms of genesis of the primary salinity and subsequent hydrochemical evolution. The total dissolved ions range from 5263 to 88,800 mg/L and 5148 to 47,145 mg/L in the lower and middle region, respectively.The saline waters and brines are characteristically Na–Cl type enriched in Ca and Sr on the one hand and depleted in Mg and SO4 on the other, relative to the seawater evaporation trend. Ionic ratios, Na–Cl–Br systematic and divalent cations suggest two likely sources of primary salinity: a fossil seawater source and dissolution of halite. However, water–rock interaction involving Mg uptake by clay minerals and possibly dolomitization during diagenesis appear to be responsible for further modification of the primary chemistry. A conceptualized hydrogeological/flow model for the brines is presented.  相似文献   

18.
腾格里沙漠地区水化学特征   总被引：8，自引：2，他引：6  
水资源极为匮乏的腾格里沙漠区内所赋存的水主要有两种类型。一种是沙下潜水 ,主要是周边山区由高向低缓慢地向沙漠区运移所致 ,分布较为普遍 ;另一种是沙漠湖水 ,它是在沙漠区内之低洼地段 ,由于沙下潜水的长期溢出汇集于大小不等的长条状湖泊之中 ,以湖表水 (咸水和卤水 )的形式存在。沙下潜水矿化度在 0 .5～ 1 g/L之间 ,为本区的饮用水。湖表水咸苦 ,矿化度较高 ,就同一湖区而言 ,也有咸水和卤水之分 ,咸水矿化度为每升数十克 ,卤水则在 1 0 0～ 440 g/L之间 ,已达到了盐湖类沉积阶段  相似文献   

19.
在调查取样的基础上,充分利用前人成果资料,应用SPSS及地下水污染分析软件,对莲花山地区区域地质条件、水化学参数空间分布特征、地下水化学类型、地下水化学成因进行分析研究,认为：莲花山地区地下水的硬度较高且矿化度较大;HCO3-浓度的平均值最大,在地下水的离子中占据主导地位;TDS（溶解性总固体）浓度较高且不同区域间浓度相差较大;莲花山地区部分区域偏硅酸、锶达到矿泉水标准,是矿泉水开发潜力区;研究区Na+和K+同时来自岩盐和硅酸岩的溶解;研究区浅层地下水中的Ca2+和Mg2+主要来源于碳酸盐的溶解;莲花山地区浅层地下水发生了阳离子交换作用.  相似文献   

20.
罗布泊盐湖钙芒硝岩孔隙中蕴藏有超大型规模的卤水钾矿,富钾卤水成因一直备受关注。罗北凹地从统一的罗布泊大湖区中分隔出来后,成盐过程中其湖水仍以南部大湖的补给为主,罗北凹地卤水化学演化与"大耳朵"湖水密切相关。"大耳朵"湖区含石膏碎屑层普遍储藏有卤水,应该是罗北凹地盐湖的"源卤水",钾离子(ρ(K~+)为3.12 g/L左右)已初步富集,平均矿化度为198.83 g/L。为了查明该卤水的化学演化趋势及析盐序列,笔者于2009年、2010年两次采集了大量卤水样品,分别进行室内等温蒸发和自然蒸发实验。蒸发实验结果表明:随着卤水浓缩首先析出(硬)石膏,随后析出大量石盐,最后出现少量钾石盐和光卤石,与EQL/EVP卤水蒸发模型模拟结果相似。将碎屑层卤水蒸发过程中化学组成变化与罗北凹地卤水进行对比,结果显示罗布泊古湖水蒸发至石膏沉积之后,在罗北凹地水化学组成明显发生变化,没有大量石盐沉积,而以钙芒硝沉积为主。推测应是受到深部"富钙水"的持续补给,而"大耳朵"湖起到"预备盆地"的作用,罗布泊古湖水经"大耳朵"湖蒸发浓缩后,钾离子得到初步富集,在流入罗北凹地后与深部"富钙"水混合,强烈蒸发浓缩,大量钙芒硝矿物析出,最后形成富钾卤水。  相似文献   

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