西藏北羌塘盆地多格错仁地区盐泉水化学特征及其物质来源

西藏北羌塘盆地是我国侏罗系海相找钾的主要远景区之一,在多格错仁地区发育有一系列具有明显的含钾异常的现代盐泉,研究这些盐泉水的物质来源具有重要的找钾意义和科学价值。野外采集了40个盐泉水的样品,并在室内测定了其化学组分、δ34 S和87 Sr/86 Sr。分析结果显示,盐泉水具有富Na+、Ca2+、K+、Cl-,贫Mg2+、SO2-4、HCO-3的特征,其Cl-含量约占矿化度的50%以上,并与矿化度呈正相关关系,Na+、Ca2+、K+浓度也与矿化度呈正相关关系。根据盐泉水的钠氯系数和溴氯系数判断,盐泉水属于地层溶滤水;源泉河、东温泉、多格错仁湖南岸3处的盐泉水具有与侏罗纪海水相一致的硫同位素特征,表明其在地下运移时,很可能溶解了地层中的石膏沉积;盐泉水的1000/Sr-87Sr/86Sr投点图说明各处盐泉水在地下的运移路径和形成过程明显不同;盐泉水的87Sr/86Sr值与其区域背景值对比显示,盐泉水在形成过程中可能溶滤了夏里组二段和索瓦组一段中的蒸发岩,区内夏里组和索瓦组最有可能蕴含有成盐成钾层系。     

四川省盐源县盐泉的特征与形成

研究天然盐泉的形成有助于揭示陆地水文循环过程中的物质迁移。采用水文地球化学的方法,分析四川省盐源县的9个泉水和卤水水样的水化学特征和同位素特征,探讨盐泉的溶质来源,总结盐泉的成因模式。水样可以分为TDS为311.69 g/L的Cl-Na型卤水、TDS为55.77~89.43 g/L的Cl-Na型盐泉、TDS为1.17 g/L的Cl-Na型微咸泉和TDS为0.26~0.56 g/L的以HCO₃-Ca、HCO₃·SO₄-Ca·Mg型为主的淡水泉。泉水和卤水的氢氧同位素显示其来源于大气降水;水样的特征系数显示盐泉和卤水都属于溶滤型,且指示研究区基本不具有找钾前景。泉水的盐分主要来源于石盐、方解石、石膏和白云石等矿物的溶滤。盐泉的形成模式可以概括为:在山区获得大气降水入渗补给后,地下水经历较浅和较深的地下径流并且溶滤含盐地层或者盐矿,使其矿化度升高,在地形较低处汇集出露地表成泉。     

西藏多格错仁南岸钙华地球化学特征与钾盐地质意义

西藏多格错仁南岸地区发育有一系列正在沉积的钙华丘和盐泉,泉水具有较高的含钾异常,属于含钾溶滤卤水,因此确定泉水中的矿物质来源成为找钾的关键问题,研究钙华的地球化学特征和成因机制则有助于解决这一问题。区内钙华有原地钙华和碎屑钙华两种类型,且明显富集K、Fe等元素,具有明显的轻稀土富集特征。不同泉眼周围的钙华样品的稀土分配模式基本相同,表明区内钙华的钙物质具有同一来源层位。经过将钙华与区内主要地层的稀土元素特征进行比对,发现这些钙华和索瓦组具有明显的亲缘关系,针对两者的相关性分析也再次表明钙华和索瓦组的亲缘特征。在此基础上,结合区内古地理和古气候资料,认为索瓦组具有较好的找钾潜力。此外,盐泉和钙华的碳、氢、氧同位素数据说明,盐泉的水物质属于大气降水,形成钙华的CO₂则具有深部来源特征,研究区的钙华属热成因钙华。     

新疆库车盆地盐泉水水化学特征、来源及找钾指示意义

库车盆地是塔里木盆地的一个次级凹陷,位于新疆塔里木陆块北缘与西南天山之间。文章介绍了库车盆地盐泉水的化学特征、来源及其找钾指示意义。对库车盆地几个代表性盐泉出露区进行盐泉水样品(21件)采集和分析,研究了其化学组成特征、水化学类型和氢氧同位素组成,同时根据收集的129件盐泉水化学数据资料,生成了盐泉水水化学分布图。新采自库车盆地的21件盐泉水样品矿化度范围为120.216~305.322g/L,水型以氯化物型(瓦里亚什科分类法)为主,具有明显的深部地层氯化钙型卤水的特征。氢氧同位素组成分析发现,盐泉水δ18 O范围为-9.1‰~4.7‰,δ2 H值范围为-75‰~-28‰,投点偏离大气降水线且δ18 O和δ2 H具有一定的正相关关系(r=0.81),表明该区盐泉水曾受到强烈蒸发作用影响,同时也受水—岩作用影响,存在一定的δ18 O漂移现象。库车盆地盐泉水组成特征与深部岩层岩性有密切关系,而断裂控制盐泉水出露与分布,盐泉水形成的地表地球化学异常对于该区找钾有一定的指示意义。     

老挝甘蒙钾盐矿床钾镁盐矿层中裂隙水的地球化学特征及其成因探讨

老挝钾盐矿所属的呵叻盆地是世界上最大的钾盐矿集区之一,矿物组合主要为石盐、光卤石和次生钾石盐等,裂隙水分布于钾镁盐矿层中(深度150m左右)。裂隙水渗漏已严重影响了矿区生产安全,但关于该水体的来源及演化过程仍不明确。本文系统采集矿层中裂隙水及周围各种水体样品12件,并测试其水化学及氢氧(2 H、18 O)同位素组成。结果表明裂隙水矿化度较高(368.1g/L~430.7g/L),裂隙水与盐泉水水化学类型同为氯化物型,分析常微量离子含量特征及水化学特征系数,显示裂隙水受到钾镁盐溶滤掺杂的影响。裂隙水δD=-64.2‰~-55.2‰,δ~(18) O=-7.75‰~-7.1‰,其比值范围显著区别于石盐(δD=-144‰~-78‰,δ~(18) O=-1.1‰~4.2‰)和钾镁盐(δD=-54.75‰~-1.42‰,δ~(18) O=-7.09‰~0.95‰)沉积阶段原始卤水氢氧同位素组成,而位于全球大气降水线附近,表明裂隙水不具有原始残留卤水特征,而主要由大气降水溶滤蒸发岩矿物所形成。裂隙水成因的查明为该区地下水循环和钾盐矿床开发过程中地下水渗漏治理提供了一定依据。     

内蒙古额济纳平原地下水氢氧稳定同位素和水化学特征及其演化规律

【研究目的】为研究内蒙古额济纳平原地下水水化学特征及其演化规律,于2020年8月采集水样87组,氢氧同位素样品69组。【研究方法】综合运用数理统计、离子比例分析、水文地球化学模拟等方法,分析额济纳平原第四系地下水及北部白垩系地下水水文地球化学特征,探讨水文地球化学演化规律。【研究结果】结果表明：(1)该区地下水水化学类型以SO₄-Na型为主。地下水中阴离子以SO₄^2-为主,其次为Cl^-;阳离子以Na⁺为主,Ca²⁺与Mg²⁺浓度差异不大。(2)研究区地下水SO₄^2-、Cl^-、TDS、总硬度、Na⁺和Mg²⁺浓度具有第四系承压水>第四系潜水>白垩系承压水的特点。(3)第四系潜水离子组分主要受溶滤作用、混合作用控制,局部地区受蒸发作用影响显著;第四系承压水离子组分主要受溶滤作用和阳离子交换作用控制;平原北部白垩系承压水...     

车马碧引水隧洞近场区水文地球化学特征及成因浅析

地下水水文地球化学特征及其成因的认识可为地下水环境及饮用水安全提供重要依据。本文以车马碧水库引水隧洞近场区为研究对象，在现场水文地质调查和分析基础上，选取33组水样进行水化学测试，并从中抽取22组水样进行氢氧同位素测定。利用Piper三线图、Gibbs模型图、离子比例分析和因子分析等方法，确定研究区地下水离子组分来源。结果表明：大气降水是研究区内地下水的主要补给来源。地下水和地表水受含水层岩性影响，主要水化学类型分别为HCO₃-Ca·Mg型、HCO₃-Ca型；支洞水由于受人类活动影响较大，阴离子由HCO₃^-型变为SO₄^2-型。水-岩作用在各离子来源中占主导作用，K⁺+Na⁺和Cl^-主要来源于盐岩和硅酸盐的溶解作用，Ca²⁺、Mg²⁺、HCO₃^-、SO₄^2-主要来...     

青海马海盐湖低品位固体钾矿室内溶矿实验研究

柴达木盆地马海盐湖浅部赋存有储量可观的低品位固体钾盐资源,通过水溶开采即固液转化的方法为企业10万吨/年的钾肥生产提供了资源保障。随着水溶开采工作的持续进行,目前马海钾矿区北部浅部固体钾矿的品位进一步降低,给盐田和选矿工艺的调整带来极大挑战。为使这部分资源得以充分利用,本文以马海盐湖钻孔9-13和9-3附近埋深0～3m的固体钾矿样品为研究对象,系统开展了室内溶矿模拟实验。实验结果表明:(1)在固体钾矿KCl品位较低时,适当提高溶剂的波美度,有利于K⁺的溶出,提高溶出液中K⁺的浓度。(2)溶剂中Na⁺的浓度太低会溶解盐层骨架,而Na⁺的浓度太高会导致结盐,生产中应根据钾矿层的实际情况,以满足溶出液K⁺浓度含量达标为准调整溶剂的波美度。(3)随着马海矿区固体钾矿品位持续降低,当K⁺的浓度达到盐田生产要求时,钠盐池卤水中Na⁺的浓度会明显增加,卤水中SO₄^2-相对浓度也相应增加,钠盐池阶段析出的石...     

新疆库车盆地富钾盐泉水化学特征与成钾显示

库车盆地古近系—新近系发育一套巨厚的膏岩盐层,钻探勘查显示,在拜城凹陷南缘5100 m深古近系库姆格列木群地层中发现钾石盐矿物。本研究采集并分析了多件盐泉水化学组成,结果显示7件盐泉水矿化度在117.7～299.4 g/L之间,钾含量在15.25～45.68 g/L之间,明显富钾,是以往报道数据(低于1 g/L)的几十倍,属于新疆首次发现。根据水化学分类,富钾盐泉水以氯化物型水为主,是Ca-Cl型卤泉水;水化学特征系数表明泉水具有高K×10~3/Cl和nK/nBr值、低的nMg/nCl和Br×10~3/Cl值(nCl~-=nNa~++nK~+)特征。同时,盐泉水均落在25℃Na~+, K~+,Mg~(2+)//Cl~-,SO■-H_2O五元水盐体系钾石盐相区,说明盐泉水可能溶滤了地层中的钾石盐,且受强烈构造挤压,沿地层断裂带或裂隙通道出露地表。库车盆地富钾盐泉水的发现,是新疆库车盆地含盐系地层存在固体钾盐的初步证据,对钾盐勘查的重点远景区具有重要的指示意义。     

东坪金矿床的围岩蚀变和流体特征

东坪金矿床围岩蚀变特征、流体包裹体特征与氢氧同位素特征研究表明,成矿流体富集K⁺、Na⁺、Au⁺、Cl^-和CO₂、H₂S,成矿溶液以岩浆热液为主,但有天水的混合。金在溶液中以Au(HS)₂^-和AuCl₂^-形式存在,构造活动引起的压力突变和流岩反应是引起金沉淀的主要因素。围岩蚀变以钾化为主,其次是硫化、钠化和硅化、碳酸盐化。金矿化与K/Al值呈反相关,与Na/Al值和S/Fe呈正相关。K/Al值的最高点与Na/Al值的最低点的对应关系可以用于圈定矿体。     

我国钾盐找矿规律新认识和进展

本文通过对比研究国内外钾盐矿床成钾特征,总结出了我国海、陆相成盐盆地和成盐成钾特性:成盐具有多期性、成盐时代差异性、成盐作用迁聚性、物质成分多样性、后期盐盆地的变动性和多液态矿的特点;厘定了3个盐类成矿域和1个成矿带;提出了我国找钾策略——以海相蒸发盐盆地为主攻方向、兼探陆相盐湖及含钾地下卤水;提出了我国主要的古代盐盆地多产于“准克拉通(陆块)”,特别是海相盐盆地均发育于前寒武纪为基底的陆块中,以及钾盐沉积于构造稳定区中相对活动的亚稳定区和在构造亚稳定区中聚集于相对稳定区的新认识;发展了适合中国地质特点的找钾理论认识,有效地推动了油钾兼探工作.发现滇西南—羌北中上侏罗统若干钾盐显示,特别是指导和部署滇西南深部侏罗纪找钾,并取得超常规的进展;进一步缩小陕北奥陶系找钾包围圈;引领“油钾兼探”实施,实现了塔里木盆地库车凹陷古近系找钾的重大实质性进展;在柴达木盆地西部发现新的早第四纪富钾层位;指导和取得青藏高原特种盐湖综合找锂、钾和评价的重要进展,新发现一批大中型锂、钾特种盐湖(特别是多格错仁大型锂、硼(钾)盐湖)和取得综合利用工艺新进展.     

Origin of groundwater salinity in the Fasa Plain,southern Iran,hydrogeochemical and isotopic approaches

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.     

碳氧同位素水文地球化学方法在找钾中的应用

在系统测定和分析了云南兰坪-思茅盆地调查区盐系地层，钾矿层中碳酸盐以及盐系HCO3^-的碳（^13C)，氧（^18O)同位素组成的基础上，发现了含钾盐泉的同位素组成特征和影响盐泉HCO3^-同位素组成的一些因素，结果确定了对找钾有利的盐泉，经与其他找钾方法确定含钾异常有较好的吻合性，表明用碳酸盐同位素方法找钾有良好的前景。     

Identifying sources of salinization using hydrochemical and isotopic techniques, Konarsiah, Iran

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.     

Integration of geochemical and isotopic tracers for elucidating water sources and salinization of shallow aquifers in the sub-Saharan Drâa Basin,Morocco

In the arid sub-Saharan of southern Morocco, groundwater salinization poses a direct threat for agricultural production in six oases’ basins that are irrigated by water imported from the High Atlas Mountains. Here the geospatial distribution of salinity is evaluated in shallow groundwater, springs and surface waters in the Drâa Basin, integrating major and trace element geochemistry and isotopic tracers (O, H, Sr and B). The data show that water discharge from the High Atlas Mountains to the Upper section of the Drâa Basin is characterized by both low and high salinity, a distinctive low δ¹⁸O and δ²H composition (as low as −9‰ and −66‰, respectively), typical for meteoric water from high elevation, a ⁸⁷Sr/⁸⁶Sr range of 0.7078–0.7094, and δ¹¹B of 12–17‰. The Ca–Mg–HCO₃, Na–Cl–SO₄, and Ca–SO₄ compositions as well as the Br/Cl, ⁸⁷Sr/⁸⁶Sr, and δ¹¹B values of the saline water suggest dissolution of Lower Jurassic carbonates and evaporite rocks in the High Atlas Mountain catchment. Storage and evaporation of the imported water in a man-made open reservoir causes an enrichment of the stable isotope ratios with a δ¹⁸O/δ²H slope of <8 but no change in the Sr and B isotope fingerprints. Downstream from the reservoir, large salinity variations were documented in the shallow groundwater from the six Drâa oases, with systematically higher salinity in the three southern oases, up to 12,000 mg/L. The increase of the salinity is systematically associated with a decrease of the Br/Cl ratio, indicating that the main mechanism of groundwater salinization in the shallow aquifers in the Drâa oases is via salt dissolution (gypsum, halite) in the unsaturated zone. Investigation of shallow groundwater that flows to the northern Drâa oases revealed lower salinity (TDS of 500–4225) water that is characterized by depleted ¹⁸O and ²H (as low as −9‰ and −66‰, respectively) and higher ⁸⁷Sr/⁸⁶Sr ratios (∼0.7107–0.7115) relative to irrigation water and groundwater flow from the Upper Drâa Basin. This newly-discovered low-saline groundwater with a different isotopic imprint flows from the northeastern Anti-Atlas Jabel Saghro Mountains to the northern oases of the Lower Drâa Basin. This adjacent subsurface flow results in a wide range of Sr isotope ratios in the shallow oases groundwater (0.7084–0.7131) and appears to mitigate salinization in the three northern Drâa oases. In contrast, in the southern oases, the higher salinity suggests that this mitigation is not as affective and increasing salinization through cycles of water irrigation and salt dissolution appears inevitable.     

藏北多格错仁红层及孢粉组合特征

青藏高原北部羌塘地块广泛出露第三纪陆相红层 ,确定这些红层及其变形的时代对认识青藏高原的形成演化过程具有非常重要的意义。 1998～ 1999年 ,INDEPTH III项目地质课题组人员 2次深入西藏可可西里地区进行科学考察 ,新发现藏北多格错仁红层 ,并在其中发现较多种属的孢粉化石。该孢粉组合反映以温带旱生草原为主体的古植被面貌。通过对青藏高原北部及邻区主要新生代盆地孢粉组合与古环境演化的对比分析 ,结合多格错仁红层上覆弱变形玄武岩 2 5～ 3 2Ma的40 Ar- 3 9Ar高精度测年资料 ,推断多格错仁红层的形成时代为晚中新世 ,多格错仁红层挤压变形所致的约 5 0 %的地壳缩短量发生在中新世末—上新世初。这些资料为建立青藏高原动力学模式提供了新的年代依据     

Factors controlling mechanisms of groundwater salinization and hydrogeochemical processes in the Quaternary aquifer of the Eastern Nile Delta, Egypt

In this study, combining interpretations of conservative dissolved ions and environmental isotopes in water were used to investigate the main factors and mechanisms controlling groundwater salinization and hydrogeochemical processes in the Eastern Nile Delta, Egypt. Hydrogeochemical and isotopic study has been carried out for 61 water samples from the study area. Total dissolved solid (TDS) contents of groundwater are highly variable rising along flowpath from the south (410 mg/L) to the north (14,784 mg/L), implying significant deterioration and salinization of groundwater. Based on TDS and ionic ratios, groundwater samples were classified into three groups. In low-saline groups, water chemistry is greatly influenced by cation exchange, mineral dissolution/precipitation, anthropogenic pollutants and mixing with surface water. Whilst, in high-saline groups, water chemistry is affected by salt-water intrusion, reverse cation exchange and evaporation. The chemical constituents originating from saline water sources, reverse ion exchange and mineral dissolution are successfully differentiated using ionic delta and saturation index approaches. The δ¹⁸O–δ²H relationship plots on a typical evaporation line, suggesting potential evaporation of the recharging water prior to infiltration. Isotope evidence concludes that the groundwater have been considerably formed by mixing between depleted meteoric water recharged under different climatic conditions and recently infiltrating enriched surface water and excess of irrigation water. The δ¹⁸O data in conjunction with chloride concentrations provide firm evidence for impact of dissolution of marine-origin evaporite deposits, during past geologic periods, on groundwater salinity in the northern region. Moreover, the relation between ¹⁴C activities and Cl^? concentration confirms this hypothesis.     

Dissolved inorganic carbon (DIC) and hydrologic mixing in a subtropical riverine estuary,southwest Florida,USA

Physical and chemical parameters were measured in a subtropical estuary with a blind river source in southwest Florida, United States, to assess seasonal discharge of overland flow and groundwater in hydrologic mixing. Water temperature, pH, salinity, alkalinity, dissolved inorganic carbon (DIC), δ¹⁸O, and δ¹³C_DIC varied significantly due to seasonal rainfall and climate. Axial distribution of the physical and chemical parameters constrained by tidal conditions during sampling showed that river water at low tide was a mixture of freshwater from overland flow and saline ground-water in the wet season and mostly saline groundwater in the dry season. Relationships between salinity and temperature, δ¹⁸O, and DIC for both the dry and wet seasons showed that DIC was most sensitive to seawater mixing in the estuary as DIC changed in concentration between values measured in river water at the tidal front to the most seaward station. A salinity-δ¹³C_DIC model was able to describe seawater mixing in the estuary for the wet season but not for the dry season because river water salinity was higher than that of seawater and the salinity gradient between seawater and river water was small. A DIC-δ¹³C_DIC mixing model was able to describe mixing of carbon from sheet flow and river water at low tide, and river water and seawater at high tide for both wet and dry seasons. The DIC-δ¹³C_DIC model was able to predict the seawater end member DIC for the wet season. The model was not able to predict the seawater end member DIC for the dry season data due to secondary physical and biogeochemical processes that altered estuarine DIC prior to mixing with seawater. The results of this study suggest that DIC and δ¹³C_DIC can provide additional insights into mixing of river water and seawater in estuaries during periods where small salinity gradients between river water and seawater and higher river water salinities preclude the use of salinity-carbon models.