Fractionation of hydrogen and oxygen isotopes of gypsum hydration water and assessment of its geochemical indications

Fundamental knowledge of the isotopic fractionation between the hydration water and the mother solution and whether the primary information recorded in hydration water can be preserved or not in deposits or mines have long been unclear. In order to calculate the accurate hydrogen and oxygen isotopic fractionation factors between gypsum hydration water and its mother solution with new methods, to understand the mechanism of fractionation and synthetically assess the record-keeping abilities of the isotopic composition of hydration water during the process of diagenesis after deposition, experiments on the hydrogen and oxygen isotopic compositions of gypsum hydration water and its mother solution at different isothermal temperatures from 5 to 50°C were systematically conducted. In addition, samples from two typical gypsum deposits formed in different environmental conditions were also determined. Results show that during gypsum crystallisation, both hydrogen and oxygen isotopes show significant fractionation between the hydration water and the mother solution. The calculated hydrogen isotopic fractionation factors are <1, while the oxygen isotopic fractionation factors are >1 at temperatures from 5 to 50°C. The fractionation factors show no functional relationships with temperature. Isotopic compositions of gypsum hydration water in arid lake sediments can be used to trace the source of water and primary deposit environmental information. However, the isotopic composition of the gypsum hydration water can easily be altered by dissolution and secondary precipitation of gypsum during later diagenesis, particularly in areas with humid climate and abundant groundwater. A very careful assessment on record-keeping abilities of the primary isotopic composition of hydration water in gypsum during later diagenesis must be considered before application.     

Anhydrite–gypsum transition in the argillites of flooded salt workings in eastern France

This study aims at understanding the physico-chemical interactions between the saturated brine and the rocks enclosing the underground salt workings in Lorraine (eastern France). These anhydrite-rich and argillaceous rocks were characterized in terms of mineralogy, micro-texture and connected porosity. Then, the two main lithofacies, massive anhydrite and anhydrite-rich argillite, were immersed in brine during more than 1 year. During this batch experiment, the argillites were affected by macroscopic splitting, contrarily to the massive anhydrite. Micro-texture and brine chemical analyses clearly show the swelling due to the hydration of anhydrite into gypsum inside the argillites, whereas hydration occurs superficially on the massive anhydrite, due to its very low permeability. Anhydrite–gypsum transformation is promoted by the presence of dissolved strontium and potassium in saturated brine. The low activity of water in saturated brine does not allow the clay fraction to swell significantly during the experiment. Thus, the expansion resulting from the hydration of anhydrite into gypsum might be responsible of the splitting of argillite in a saturated brine environment. The superficial anhydrite hydration on massive anhydrite can be explained by the low amount of connected porosity (less than 1%).     

The origin and significance of groundwater-seepage gypsum from Bristol Dry Lake, California, USA

Gypsum and anhydrite fabrics observed in trenches and deep (500 m) cores from Bristol Dry Lake, California, USA, exhibit a vertical alignment of crystals similar to the fabric seen in bottom-nucleated brine pond gypsum. However, geochemical and sedimentological evidence indicate that the gypsum formed in Bristol Dry Lake precipitated displacively within the sediment where groundwater saturated with respect to gypsum recharges around the playa margin (groundwater-seepage gypsum). Evidence for displacive growth of gypsum is: (i) the geometry of the deposit, (ii) stable isotopic data and the water chemistry of the brine, and (iii) inclusions of matrix which follow twin planes and completely surround crystals as they grow. The bulk of the gypsum precipitated in the playa occurs around the edges of the playa in the playamargin facies and completely rings the lake. Sulphate concentrations in the groundwater increase toward the gypsum zone in the playa margin. Basinward of this zone, sulphate concentrations decrease sharply to trace element levels in the basin centre brine. Authigenic gypsum is rare in the centre of the playa. Stable (δ¹⁸O values measured for gypsum waters of crystallization (GWC) are similar to the values calculated for groundwater in the playa margin and alluvial fan sediments (?– 6%0), whereas measured brine δ¹⁸O values range from + 0·5 to + 3·7%0. Deuterium values measured for groundwater are ?– 70%0, GWC are ?– 60 to – 65%0 and brine values are ?– 57%0. The geometry of the deposit and the chemical data suggest that the water precipitating the gypsum is more closely associated with the groundwater than the brine. However, some mixing between groundwater and brine is likely. Within 100 m of the surface, the gypsum dehydrates to anhydrite, although the same vertically aligned fabric is retained through the diagenetic process. The similarity of displacive vertically aligned gypsum and anhydrite fabrics seen in Bristol Dry Lake to subaqueously deposited gypsum in modern brine ponds indicates that the criteria used to define subaqueous fabrics must be better constrained.     

Holocene stromatolites and microbial laminites associated with lenticular gypsum in a marine-dominated environment, Ras El Shetan area, Gulf of Aqaba, Egypt

Field and petrographic investigations of Holocene evaporites in the Ras El Shetan area, Gulf of Aqaba, Egypt, indicate the presence of microbial mats either in the form of laminites or stromatolites. The morphology of microbial mats and gypsum crystal size characterize the following lithofacies: (1) slump-stromatolitic gypsarenite, (2) random gypsrudite, (3) stromatolitic gypsarenite, and (4) microbially laminated gypsrudite. These evaporite lithofacies are formed above pre-evaporitic mudstones rich in disrupted cyanobacterial filaments, burrows and cerithid gastropods. The morphology of the gypsum crystals is mainly lenticular, indicating enrichment of dissolved organic compounds in the depositional environment. The difference in size of the lenticular gypsum crystals is related to minor changes in salinity and temperature of the parent brine. Fluid inclusions in gypsum crystals indicate their formation at low temperature (<50°C) in a seawater sourced brine that evaporated to gypsum saturation or higher. The brine salinities range from 10·62 to 12·99 equivalent wt% NaCl, and the brine densities range from 1·08 to 1·11 g/cm³. The change in morphology of the microbial mats (stromatolites and laminites) is related mainly to changes in water depth, from a very shallow salina to a coastal sabkha. Lenticular gypsum nucleated displacively in the microbial mats from saline, oxygenated groundwater that seeped from the sea through a barrier.     

四川盆地海相三叠系硬石膏和盐卤水的硫同位素组成及意义

四川盆地下、中三叠统硬石膏和盐卤水广布，通过对采集于不同地段不同层位各具代表性的硬石膏、石膏和盐卤水的２４４件样品的分析，可见其同层位硫同位素组成稳定，δ３４Ｓ自下而上具阶梯状递减轻化的趋势，与已知全球海相三叠系硫同位素组成有明显差异。这种硫同位素分布规律对地层划分和对比、蒸发岩形成环境的判断、研究卤水产层和成因、掌握蒸发岩咸化发展方向及预测找钾工作等的意义不容忽视。     

Kinetics of gypsum nucleation and crystal growth from Dead Sea brine

The Dead Sea brine is supersaturated with respect to gypsum (Ω = 1.42). Laboratory experiments and evaluation of historical data show that gypsum nucleation and crystal growth kinetics from Dead Sea brine are both slower in comparison with solutions at a similar degree of supersaturation. The slow kinetics of gypsum precipitation in the Dead Sea brine is mainly attributed to the low solubility of gypsum which is due to the high Ca²⁺/SO₄²⁻ molar ratio (115), high salinity (∼280 g/kg) and to Na⁺ inhibition.Experiments with various clay minerals (montmorillonite, kaolinite) indicate that these minerals do not serve as crystallization seeds. In contrast, calcite and aragonite which contain traces of gypsum impurities do prompt precipitation of gypsum but at a considerable slower rate than with pure gypsum. This implies that transportation inflow of clay minerals, calcite and local crystallization of minerals in the Dead Sea does not prompt significant heterogeneous precipitation of gypsum. Based on historical analyses of the Dead Sea, it is shown that over the last decades, as inflows to the lake decreased and its salinity increased, gypsum continuously precipitated from the brine. The increasing salinity and Ca²⁺/SO₄²⁻ ratio, which results from the precipitation of gypsum, lead to even slower kinetics of nucleation and crystal growth, which resulted in an increasing degree of supersaturation with respect to gypsum. Therefore, we predict that as the salinity of the Dead Sea brine continues to increase (accompanied by Dead Sea water level decline), although gypsum will continuously precipitate, the degree of supersaturation will increase furthermore due to progressively slower kinetics.     

新疆罗布泊盐湖氢氧锶硫同位素地球化学及钾矿成矿物质来源

罗布泊罗北凹地第四系上部盐层中蕴藏丰富的卤水,卤水中则富含钾（ＫＣｌ平均品位为１．４０％）。文章通过对罗布泊卤水氢、氧、锶及硫同位素等分析及与塔里木盆地（河流）、柴达木盆地等地区对比研究,确定了罗布泊富钾卤水源于地表水,可能主要是塔里木盆地南北缘河流水;卤水中的硫钾等物质组分主要来源于南天山、塔里木盆地西北、西南部中新生代石膏钙芒硝石盐矿床或地层及其古代地层卤水。由于第四纪期间塔里木盆地西部抬升。     

Diagenetic formation of gypsum and dolomite in a cold‐water coral mound in the Porcupine Seabight,off Ireland

Authigenic gypsum was found in a gravity core, retrieved from the top of Mound Perseverance, a giant cold‐water coral mound in the Porcupine Basin, off Ireland. The occurrence of gypsum in such an environment is intriguing, because gypsum, a classic evaporitic mineral, is undersaturated with respect to sea water. Sedimentological, petrographic and isotopic evidence point to diagenetic formation of the gypsum, tied to oxidation of sedimentary sulphide minerals (i.e. pyrite). This oxidation is attributed to a phase of increased bottom currents which caused erosion and enhanced inflow of oxidizing fluids into the mound sediments. The oxidation of pyrite produced acidity, causing carbonate dissolution and subsequently leading to pore‐water oversaturation with respect to gypsum and dolomite. Calculations based on the isotopic compositions of gypsum and pyrite reveal that between 21·6% and 28·6% of the sulphate incorporated into the gypsum derived from pyrite oxidation. The dissolution of carbonate increased the porosity in the affected sediment layer but promoted lithification of the sediments at the sediment‐water interface. Thus, authigenic gypsum can serve as a signature for diagenetic oxidation events in carbonate‐rich sediments. These observations demonstrate that fluid flow, steered by environmental factors, has an important effect on the diagenesis of coral mounds.     

The behavior of lithium and its isotopes in oilfield brines: evidence from the Heletz-Kokhav field, Israel

Twenty-four brine samples from the Heletz-Kokhav oilfield, Israel, have been analyzed for chemical composition and Li isotope ratios. The chemical composition of the brines, together with geological evidence, suggests derivation from (Messinian) seawater by evaporation that proceeded well into the gypsum stability field but failed to reach the stage of halite crystallization. The present salinity of the samples (18-47 g Cl/L) was achieved by dilution of the original evaporitic brine by local fresh waters. Like brines from other sedimentary basins, the Li/Cl ratios in the Heletz-Kokhav samples show a prominent Li enrichment (five-fold to eight-fold) relative to modern seawater. The isotopic ratios of Li, expressed in the δ ⁶Li notation, vary from −26.3 to −17.9‰, all values being significantly higher than that of modern seawater (−32‰) irrespective of their corresponding Li concentration (1.0-2.3 mg/L). The isotopic composition of Li and the Li/Cl ratio in the oilfield brines were acquired in two stages: (a) The original evaporated seawater gained isotopically light Li during the diagenetic interaction between the interstitial Messinian brine and the basin sediments. A parent brine with an elevated Li/Cl ratio was formed. The brine was later diluted in the oilfields. (b) The δ ⁶Li values of the final brines were determined during epigenetic interaction with the Heletz-Kokhav aquifer rocks. At the same time, the Li/Cl ratio inherited from stage (a) remained largely unchanged. This work represents the first use of lithium isotopic composition to elucidate the origin and evolution of formation waters in sedimentary basins.     

罗布泊盐湖富钾卤水成因再探讨——碎屑层卤水蒸发实验分析

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。     

He-Ar Isotopic Systematics of Fluid Inclusions in Pyrites from PGEpolymetallic Deposits in Lower Cambrian Black Rock Series, South China

He-Ar isotopic compositions of fluid inclusions trapped in pyrites from some representative PGE-polymetallic deposits in Lower Cambrian black rock series in South China were analyzed by using an inert gas isotopic mass spectrometer. The results show that the ore-forming fluids possess a low 3He/4He ratio, varying from 0.43×10-8 to 26.39×10-8, with corresponding R/Ra value of 0.003-0.189. The 40Ar/36Ar ratios are 258-287, close to those of air saturated water (ASW). He-Ar isotopic indicator studies show that the ore-forming fluids were mainly derived from the formation water or basinal hot brine and sea water, while the content of mantle-derived fluid or deep-derived magmatic water might be negligible. The PGE-polymetallic mineralization might be related to the evolution of the Caledonian miogeosynclines distributed along the southern margin of the Yangtze Craton. During the Early Cambrian, the formation water or basinal hot brine trapped in Caledonian basins which accumulated giant thick sediments was     

Determination par activation neutronique des rapports Cl/Br des inclusions fluides de divers gypses. Correlation avec les donnees de la microcryoscopie et interpretations genetiques

Gypsum contains liquid inclusions which fill mainly primary cavities. Analysis of inclusions may give some information about the mineral formation process. In places, diagenetic solutions have filled secondary cavities along cleavage planes or replaced initial liquid inclusions in primary cavities; the presence of such secondary inclusions must, therefore, be taken into consideration. This study presents our results on the Cl/Br ratio of liquid inclusions in gypsum. The Cl/Br ratio is practically constant in present sea water, and has been measured in many different types of waters. The Br content of halite has also been extensively studied to trace the compositional changes of a salt-depositing brine. In gypsum Br is present only in microscopic fluid inclusions. For this reason we used the neutron-activation method. We adopted the technique in order to prevent any contamination and obtain directly Cl/Br ratio within 10% accuracy. In order to ascertain that liquid inclusions reside mainly in primary cavities of gypsum, we selected our samples only after microscopic observation. Fifty-eight samples from different types of gypsum were analysed. The salinities of the inclusions, obtained through the data on freezing, and the Cl/Br ratio, obtained through activation-analysis, give us clues as to the nature of the fluids depositing the gypsum. Recent gypsum deposits from French salt-pans of Mediterranean and Atlantic coasts were sampled. The latter has apparently been diagenetically altered by meteoric water; the salinity of many inclusions having been changed while the Cl/Br ratio (315 and 350) in both remains close to the value of present sea water (#300). Liquid inclusions of Recent crystals from New Caledonia, deposited in mangrove swamps are enriched in Br (Cl/Br = 150 and 200). The enrichment might be related to the presence of abundant organic materials. Inclusions in crystals from Sebkha el Melah (Tunisia) also show high Br content (Cl/Br = 194). In this case, the brine was highly concentrated and was saturated with NaCl. The Upper Miocene gypsum from Sicily was studied to test the various models for the genesis of this important evaporite formation of the Mediterranean. Freezing data show some decrease of salinities, probably by groundwater diagenesis, but the Br content is high. The Cl/Br ratio is 175, and this value is similar to that of Sebkha el Melah. Samples from three thick Eocene and Oligocene sequences near Paris and in the South of France were studied. Freezing data and Cl/Br ratio of their inclusions indicate that those gypsum deposits have crystallized in marine environments receiving considerable influx of river-waters.     

Biogeochemical implications of the isotopic equilibrium fractionation factor between the oxygen atoms of acetone and water

Carbonyl oxygens of organic molecules undergo isotopic exchange with water during reversible hydration reactions. The equilibrium isotopic fractionation factors between the carbonyl oxygen of acetone and water at 15°, 25°, and 35°C are 1.028, 1.028, and 1.026 respectively. The differences between the δ¹⁸O values of the carbonyl oxygen of acetone and of the water with which it is in equilibrium are similar to the differences that have been observed between the δ¹⁸O values of cellulose and the water used in its synthesis by a variety of aquatic plants and animals. Additionally, the identity of the acetone-water fractionation factors at 15° and 25°C parallels the observation that the difference between the δ¹⁸O values of cellulose and water shows no temperature dependence for individual species of plants grown over the same temperature range. These results are discussed in relation to the proposal that the oxygen isotopic relationship between cellulose and water is established by isotopic exchange occurring during the hydration of carbonyl groups of the intermediates of cellulose synthesis.     

Modern sedimentation and hydrology in Lake Tyrrell,Victoria

Lake Tyrrell is a large ephemeral salt lake, the level of which is controlled by climate and groundwater. Up to a metre of water fills the basin during the wetter and cooler winter season, but evaporates during the summer, precipitating up to 10 cm of halite. Each year essentially the same pool of ions is redissolved by this annual freshening. The small percentage of gypsum precipated (< 2%) in the surface salt crust reflects the low calcium content of the brine which, in turn, is a function of the negligible net discharge of calcium from the groundwater system. The small influx of fine‐grained clastic sediment to the lake floor comes from surface runoff, wind, and reworking of older sediment from the shoreline.

The Lake Tyrrell basin lies in a setting in which three different groundwater types, identified by distinct salinities, interact with surface waters. A refluxing cycle that goes from discharging groundwater at the basin margin, to surface evaporation on the lake floor, to recharge through the floor of the lake, controls the major chemical characteristics of the basin. In this process, salts are leached downward from the lake floor to join a brine pool below the lake. This provides an outlet from the lake, especially under conditions that have been both drier and wetter than those of today. Enhanced discharge occurs under drier conditions, when the enclosing regional groundwater divide is lowered, whereas a rise in lake level increases the hydraulic head over that of the sub‐surface brine and promotes an increase in brine loss from the lake.

Sulphate‐reducing bacteria in a zone of black sulphide‐rich mud beneath the salt crust help prevent gypsum from being incorporated into the recent sedimentary record. However, below the upper 5 to 10 cm zone of bacterial activity, discoidal gypsum is being precipitated within the mud from the groundwater. These crystals have grown by displacing the mud and typically “float” in a clay matrix; in some zones, they form concentrations exceeding 50% of the sediment. The occasional laminae of more prismatic gypsum that occur within the upper metre of mud have crystallised from surface brines. The scarcity of these comparatively pure prismatic‐crystal concentrations probably is a function of unfavourable chemical conditions in the lake brine and of the role that sulphate‐reducing bacteria have played.     

Minerogenic Theory of the Superlarge Lop Nur Potash Deposit, Xinjiang, China

Located in the eastern part of the Tarim basin, Xinjiang, the Lop Nur was an ultimate water catchment area of the Tarim basin during the Quaternary. Through nearly ten years of investigation and research, the authors have found a superlarge brine potash deposit in the Luobei subbasitv—a secondary basin of the Lop Nur depression. The deposit has been mined now. On that basis, the authors propose new theories on the genesis of the potash rock deposit. In the tectonic and geomorphologic contexts, the Tarim basin lies in a “high mountain-deep basin” environment. At the beginning of the Quaternary, influenced by the neotectonic movement, the Lop Nur evolved into a “deep basin” in the Tarim basin. At the end of the middle Pleistocene, neotectonic migration began to take place in the interior of the Lop Nur and a new secondary deep basin—the Luobei subbasin—formed gradually. Despite its small area, it is actually the deepest subbasin in the Lop Nur depression, where brines of the Lop Nur Salt Lake gather and evaporate, thus providing materials for the formation of a superlarge brine potash rock deposit. With respect to the phenomenon of brine concentration and change with deepening of the lake, the authors propose a model of “high mountain-deep basin” tectonic migration for potash concentration. In the sedimentological context, the honeycomb-shaped voids developed in glauberite rock in the subbasin are good space for potash-rich brine accumulation. Study indicates that the deposition of glauberite requires recharge of calcium-rich water.In the Tarim area the calcium-rich water might come from deep formation water or oilfield water, and the river water recharging the Lop Nur Salt Lake was rich in sulfate radicals and other components; in addition, the climate in the area was very dry and the brine evaporated steadily, thus resulting in deposition of substantial amount of glauberite, potash accumulation in intercrystal brine and final formation of the potash deposit. Generally, potash formation in a salt lake undergoes a three-stage process of “carbonates→sulfates (gypsum and glauberite)→chlorides (halite etc.)”, but in the study area there only occurred a two-stage process of “carbonates→sulfates (gypsum and glauberite)”. The authors call this new geological phenomenon the “two-stage potash formation” model. In conclusion, the superlarge Lop Nur potash deposit is the result of combined “high mountain-deep basin” tectonism and “two-stage potash formation”.     

The origin of fluids in the salt beds of the Delaware Basin,New Mexico and Texas

Oxygen and hydrogen isotope analyses have been made of (1) brines from several wells in the salt deposits of the Delaware Basin, (2) inclusion fluids in halite crystals from the ERDA No. 9 site, and (3) local ground waters of meteoric origin. The isotopic compositions indicate that the brines are genetically related and that they probably originated from the evaporation of paleo-ocean waters. Although highly variable in solute contents, the brines have rather uniform isotopic compositions. The stable isotope compositions of brine from the ERDA No. 6 site (826.3 m depth) and fluid inclusions from the ERDA No. 9 site are variable but remarkably regular and show that (1) mixing with old or modern meteoric waters has occurred, the extent of mixing apparently decreasing with depth, and (2) water in the ERDA No. 6 brine may have originated from the dehydration of gypsum. Alternatively, the data may reflect simple evaporation of meteoric water on a previously dry marine flat. Stable isotope compositions of all the waters analyzed indicate that there has been fairly extensive mixing with ground water throughout the area, but that no significant circulation has occurred. The conclusions bear importantly on the suitability of these salt beds and others as repositories for nuclear waste.     

四川渠县三叠系膏盐的同生、成岩、后生及表生变化

本文论述了四川渠县三叠系的膏盐在沉积后的不同阶段所发生的各种变化,并提出根据膏盐的变化特征推测它们的原生沉积条件、卤水咸化程度及研究区的矿床保存条件。     

Sedimentology of Badenian (middle Miocene) gypsum in eastern Galicia, Podolia and Bukovina (West Ukraine)

Primary gypsum is the main evaporite mineral in the middle Miocene (Badenian) of the West Ukraine. The lower part of the gypsum sequence is built of autochthonous gypsum while the upper part is composed of allochthonous gypsum that formed following a major, tectonically induced, change in basin morphology. This change resulted in the destruction of the gypsum deposited on the margins of the basin and formation of redeposition features. Autochthonous gypsum facies were deposited in two main environments: (1) giant gypsum intergrowths precipitated from highly concentrated brines; (2) very shallow subaqueous gypsum deposited in a vast brine pan. The brine pan was characterized by a facies mosaic that reflects an interplay of concentrated brines from the central part of the evaporite basin and diluted brines due to the influx of continental meteoric waters. The facies continuum, microbial gypsum - bedded selenite - massive selenite - sabre gypsum, indicates increasing salinity of the brine with time. This type of facies pattern has been established in recent salinas that are analogous to Badenian gypsum in their lateral facies changes. However, the pattern of facies distribution with respect to the open sea in the Badenian basin is opposite to that found in recent salinas. The pattern of the Badenian gypsum facies in the Ukraine indicates that facies repetition may have been related to climatically controlled salinity changes and not to depth changes, as is commonly used to explain the repetition of sulphate facies in a vertical succession.     

察尔汉盐湖的半水石膏及其成因分析

本文对自然界极为少见、产于青海柴达木盆地的半水石膏的矿物特征进行了详细研究,并引用实际资料及理论依据,对其成因进行了探讨。     

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。