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.
In the Western Canadian Sedimentary Basin, the petroleum industry handles two geochemically distinctive brines that are traceable in the environment: formation brines extracted along with hydrocarbons from the basin, and salt-dissolution brines, produced by dissolving deep halite formations to create caverns for petroleum product storage. The concentrations of the conservative ions chloride (Cl) and bromide (Br) in many formation brines plot closely to the seawater evaporation trajectory of previous studies. These brines contain Cl/Br mass ratios of around 300, while salt-dissolution brines are relatively Br depleted, having Cl/Br mass ratios in excess of 20,000. An oilfield site in central Alberta had experienced nearby releases of both salt-dissolution and formation brines. Geochemical mixing trends were defined by theoretically mixing samples of local salt-dissolution and formation brine sources with background shallow groundwater. Most site monitoring wells and local surface water samples plotted directly on a salt-dissolution brine dilution trend, while results from four monitoring wells, all located directly downgradient of formation brine spills, suggested the mixing of formation brines into shallow groundwater. This work indicates that there is a large-scale salt-dissolution brine plume beneath the site and reinforces the use of Cl and Br concentrations and mass ratios as environmental tracers.  相似文献   

2.
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.  相似文献   

3.
The Ca–Mg relationship in groundwaters strongly points to the overall dolomitization and local albitization. The Mg/Ca ratios reveal two trends by which saline waters develop: increase of Mg/Ca ratio by evaporation and decreasing Mg/Ca ratios due to dolomitization and albitization. Br/Cl vs. Na/Cl ratios demonstrate that albitization does not play a major role which leaves dolomitization to be the main source for decreasing Mg/Ca ratios in saline waters. In the eastern and southern Region of Lake Kinneret, salinization occurs by mixing with a Ca/Mg molar ratio <1 brine (Ha’On type). Along the western shoreline of the Lake, a Ca/Mg > 1 dominates, which developed by the albitization of plagioclase in abundant mafic volcanics and the dolomitization of limestones. The most saline groundwater of the Tabgha-, Fuliya-, and Tiberias clusters could be regional derivatives of at least two mother brines: in diluted form one is represented by Ha’On water, the other is a Na-rich brine of the Zemah type. Additionally, a deep-seated Ca-dominant brine may ascend along the fractures on the western side of Lake Kinneret, which is absent on the eastern side. Groundwaters of the Lower Jordan Valley are chemically different on both sides of the Jordan River, indicating that the exchange of water is insignificant. All saline waters from the Dead Sea and its surroundings represent a complex mixture of brines, and precipitation and local dissolution of halite and gypsum. Many wells of the Arava/Araba Valley pump groundwater from the Upper Cretaceous limestone aquifer, the origin of the water is actually from the Lower Cretaceous Kurnub Group sandstones. Groundwater drawn from the Quaternary alluvial fill either originates from Kurnub Group sandstones (Eilat 108, Yaalon 117) or from altered limestones of the Judea Group. The origin of these waters is from floods flowing through wadis incised into calcareous formations of the Judea Group. On the other hand, as a result of step-faulting, hydraulic contact is locally established between the Kurnub- and the Judea Groups aquifers facilitating the inter-aquifer flow of the confined Kurnub paleowater into the karstic formations of the Judea Group. Two periods of Neogene brine formation are considered: the post-Messinan inland lagoon resulting in drying up of the Sdom Sea and the evaporation of the Pleistocene Samra Lake, which went further through the stage of Lake Lisan to the present Dead Sea. For the first period, major element hydrochemistry suggests that the saline waters and brines in the Jordan-Dead Sea–Arava Valley transform evolved from the gradual evaporation of an accumulating mixture of sea-, ground-, and surface water. Due to the precipitation of carbonates, gypsum, and halite, such an evaporating primary water body was strongly enriched in Mg, Br, and B and shows high molar ratios of Br/Cl, B/Cl, and Mg/Ca but low Na/Cl ratios. The development of the Br/Cl ratio is chemically modelled, showing that indeed brine development is explicable that way. Along with the evaporation brine, evaporites formed which are leached by infiltrating fresh water yielding secondary brines with Na/Cl ratios of 1. When primary brines infiltrated the sub-surface, they were subjected to Mg–Ca exchange in limestones (dolomitization) and to chloritization and albitization in basic igneous rocks turning them into Ca-Cl brines. These tertiary brines are omnipresent in the Rift. The brines of the late Lisan and Dead Sea were generated by evaporating drainage waters, which leached halite, gypsum, and carbonates from the soil and from the sub-surface. All these brines are still being flushed out by meteoric water, resulting in saline groundwaters. This flushing is regionally enhanced by intensive groundwater exploitation. In variable proportions, the Neogene and late Lisan Lake and Recent Dead Sea brines have to be considered as the most serious sources of salinization of groundwaters in the Rift. Deep-seated pre-Sdom brines cannot strictly be excluded, but if active they play a negligible role only. An erratum to this article can be found at  相似文献   

4.
Analyses of halogen concentration and stable chlorine isotope composition of fluid inclusions from hydrothermal quartz and carbonate veins spatially and temporally associated with giant unconformity-related uranium deposits from the Paleoproterozoic Athabasca Basin (Canada) were performed in order to determine the origin of chloride in the ore-forming brines. Microthermometric analyses show that samples contain variable amounts of a NaCl-rich brine (Cl concentration between 120,000 and 180,000 ppm) and a CaCl2-rich brine (Cl concentration between 160,000 and 220,000 ppm). Molar Cl/Br ratios of fluid inclusion leachates range from ∼100 to ∼900, with most values between 150 and 350. Cl/Br ratios below 650 (seawater value) indicate that the high salinities were acquired by evaporation of seawater. Most δ37Cl values are between −0.6‰ and 0‰ (seawater value) which is also compatible with a common evaporated seawater origin for both NaCl- and CaCl2-rich brines.Slight discrepancies between the Cl concentration, Cl/Br, δ37Cl data and seawater evaporation trends, indicate that the evaporated seawater underwent secondary minor modification of its composition by: (i) mixing with a minor amount of halite-dissolution brine or re-equilibration with halite during burial; (ii) dilution in a maximum of 30% of connate and/or formation waters during its migration towards the base of the Athabasca sandstones; (iii) leaching of chloride from biotites within basement rocks and (iv) water loss by hydration reactions in alteration haloes linked to uranium deposition.The chloride in uranium ore-forming brines of the Athabasca Basin has an unambiguous dominantly marine origin and has required large-scale seawater evaporation and evaporite deposition. Although the direct evidence for evaporative environments in the Athabasca Basin are lacking due to the erosion of ∼80% of the sedimentary pile, Cl/Br ratios and δ37Cl values of brines have behaved conservatively at the basin scale and throughout basin history.  相似文献   

5.
柴达木盆地西北角分布有基岩,盆地西部分布山麓堆积及河、湖相沉积地层,新生界发育有多个北西—南东走向的规模不一的背斜,新近系分布有富钾地下卤水。利用统计方法分析卤水中TDS、K+和B2O3的富集情况。结果显示：TDS值出现双峰,卤水样品富K+和B3+的概率分别为628%和6129%。使用Piper图研究地下卤水时,经常出现样品点过于集中而不易反映主要离子含量的变化。本次研究改进了前人的图示方法,绘制适合于表示地下卤水的水化学图。利用钠氯系数、氯溴系数、氯碘系数、钾氯系数、脱硫系数、钙镁系数对研究区卤水水样进行分析,结果显示卤水样品多数未达到石盐沉积,少数达到石盐沉积。研究区水样氢、氧稳定同位素数据显示新近系地下卤水δ18O值和δD值均发生漂移,表明卤水经历长时间的蒸发浓缩。研究区地下卤水起源于早上新世的古大气降水,上新世以后由于青藏高原快速隆升,柴达木盆地抬升和沉降中心东移,接受沉积形成良好的盖层,同时大气环流的改变致使气候变得干燥,地下卤水经历蒸发浓缩封存,形成现今的卤水。  相似文献   

6.
A combination of analytical methods, including trace element analysis of Br in scapolite by LA‐ICP‐MS, was employed to unravel the fluid–rock interaction history of the Mary Kathleen Fold Belt of northern Australia. Halogen ratios in the metamorphic and hydrothermally derived scapolite from a range of rock‐types record interaction between the host rocks and magmatic‐hydrothermal fluids derived from granite plutons and regional metamorphism. The results show that halite‐dissolution supplied at best only minor chlorine to fluids in the Fold Belt. Chlorine/bromine ratios in metamorphic scapolite indicate that fluids were dominantly derived from basinal brines formed from sub‐aerial evaporation of seawater beyond the point of halite saturation. This bittern fluid infiltrated the underlying sedimentary sequences prior to regional metamorphism. Zoned scapolite in a major late metamorphic mineralized shear‐zone records three discrete pulses of magmatic and metamorphic fluid, and it is suggested that fluid mixing may have assisted mineralization along and around this shear‐zone. As a crucial prerequisite for halogen fluid tracer studies using scapolite, we find in our samples that Cl and Br do not fractionate when incorporated in scapolite. Furthermore, unaltered rims of heavily retrogressed scapolite show indistinguishable Cl/Br signatures compared with fresh grains from the same sample indicating retrograde metamorphism did not significantly affect Cl and Br signatures in scapolite group minerals.  相似文献   

7.
《Applied Geochemistry》2001,16(1):35-55
Formation waters within Upper Carboniferous sandstones in the sub-sea Prince and Phalen coal mines, Nova Scotia, originated as residual evaporative fluids, probably during the precipitation of Windsor Group (Lower Carboniferous) salts which underlie the coal measures. Salinity varies from 7800 to 176,000 mg/l, and the waters are Na–Ca–Cl brines enriched in Ca, Sr and Br and depleted in Na, K, Mg and SO4 relative to the seawater evaporation curve. Br:Cl and Na:Cl ratios suggest that the brine composition corresponds to an evaporation ratio of as much as 30. The brines lie close to the meteoric line on H/O isotopic plots but with a compositional range of δ18O from −4.18 to −6.99 and of δD from −42.4 to −23.5, distant from modern meteoric or ocean water. Mine water composition contrasts with that of nearby salt-spring brines, which are inferred to have originated through dissolution of Windsor Group evaporites by modern meteoric waters. However, a contribution to the mine waters from halite dissolution and from Br in organic matter cannot be ruled out. Present concentrations of several elements in the brines can be explained by water–rock interaction. The original Windsor brines probably moved up into the overlying coal-measure sandstones along faults, prior to the Late Triassic. The high salinity and irregular salinity distribution in the Phalen sandstones suggests that the brines have undergone only modest dilution and are virtually immobile. In contrast, Prince waters show a progressive increase in salinity with depth and are inferred to have mixed with surface waters. Basinal brines from which these modern formation fluids were derived may have been important agents in base-metal and Ba mineralisation from the mid-Carboniferous onwards, as saline fluid inclusions are common in Zn–Pb sulphide deposits in the region.  相似文献   

8.
《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   

9.
Large quantities of highly saline brine flow from gas wells in the Marcellus Formation after hydraulic stimulation (“fracking”). This study assesses the composition of these flowback waters from the Marcellus shale in Pennsylvania, USA. Concentrations of most inorganic components of flowback water (Cl, Br, Na, K, Ca, Mg, Sr, Ba, Ra, Fe, Mn, total dissolved solids, and others) increase with time from a well after hydraulic stimulation. Based on results in several datasets reported here, the greatest concentration of Cl− in flowback water is 151,000 mg/L. For total Ra (combined 226Ra and 228Ra) in flowback, the highest level reported is 6540 pCi/L. Flowback waters from hydraulic fracturing of Marcellus wells resemble brines produced from conventional gas wells that tap into other Paleozoic formations in the region. The Br/Cl ratio and other parameters indicate that both types of brine formed by the evaporation of seawater followed by dolomitization, sulfate reduction and subsurface mixing with seawater and/or freshwater. Trends and relationships in brine composition indicate that (1) increased salt concentration in flowback is not mainly caused by dissolution of salt or other minerals in rock units, (2) the flowback waters represent a mixture of injection waters with highly concentrated in situ brines similar to those in the other formations, and (3) these waters contain concentrations of Ra and Ba that are commonly hundreds of times the US drinking water standards.  相似文献   

10.
The Mengyejing potash deposit is located in the southern port of the Simao Basin, Yunnan Province, and is hosted in mid-Cretaceous strata. The chemical compositions of fluid inclusions in halite crystals, collected from the level-610 adit in the deposit, were analysed by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The results show that the brine is of the Na-K-Mg-Ca-Cl type and has K concentrations that are distinctly higher than those of Mg and Ca, unlike normal brines associated with Cretaceous halite. The high K concentrations indicate that the degree of evaporation of the ancient Mengyejing saline lake was very high, reaching the sylvite deposition stage but rarely reaching the carnallite deposition stage. The trajectory of the H and O isotopic compositions of the brines in the halite-hosted fluid inclusions corresponds to intense evaporation, indicating that the net evaporation exceeded the net inflow of brines. These brine compositions in halite-hosted fluid inclusions were likely formed by the dissolution of previously deposited K-bearing minerals by fresh continental and/or seawater, forming a type of modified seawater, with deep hydrothermal fluids potentially supplying additional potassium. The basin likely experienced multiple seawater incursion, dissolution and redeposition events in a high-temperature environment with high evaporation rates.  相似文献   

11.
Analyses of fluid-inclusion leachates from ore deposits show that Na/Br ratios are within the range of 75 - 358 and Cl/Br 67 - 394, respectively, and this variation trend coincides with the seawater evaporation trajectory on the basis of the Na/Br and Cl/Br ratios. The average Cl/Br and Na/Br ratios of mineralizing fluids are 185 and 173 respectively, which are very close to the ratios ( 120 and 233 ) of the residual evaporated seawater past the point of halite precipitation. It is suggested that the original mineralizing brine was derived from highly evapo-rated seawater with a high salinity. However, the inclusion fluids have absolute Na values of 69.9—2606.2 mmol kg^-1 and Cl values of 106.7 — 1995.5 mmol kg^-1. Most of the values are much less than those of seawater: Na, 485 mmol kg^-1 and Cl, 566 mmol kg^-1 , respectively; the salinity measured from fluid inclusions of the deposits ranges from 2.47 wt% to 15.78 wt% NaCl equiv. The mineralizing brine has been diluted. The δ ^18O and δD values of ore-forming fluids vary from -8.21‰ to 9.51‰ and from -40.3‰ to -94.3‰, respectively. The δD values of meteoric water in this region varied from - 80‰ to - 100‰ during the Jurassic. This evidenced that the ore-forming fluids are the mixture of seawater and meteoric water. Highly evaporated seawater was responsible for leaching and extracting Pb, Zn and Fe, and mixed with and diluted by descending meteoric water, which resulted in the formation of ores.  相似文献   

12.
Halogen ratios (Br/Cl and I/Cl) and concentrations provide important information about how sedimentary formation waters acquire their salinity, but the possible influence of organic Br derived from sedimentary wall-rocks is rarely quantified. Here, it is demonstrated that Br/Cl versus I/Cl mixing diagrams can be used to deconvolve organic Br contributions; that organic matter has a limited range of Br/I ratios; and that organic Br is a more significant component in Zn–Pb deposit ore fluids than previously recognised. The significance of these findings is illustrated for the Lennard Shelf Zn–Pb deposits of Western Australia.Fluid inclusions related to Lennard Shelf Zn–Pb mineralisation have variable salinity and hydrocarbon contents. The halogen data from these fluid inclusions require mixing of three fluid end-members: (1) an evaporated seawater bittern brine (30 wt.% NaCl equiv.) with greater than seawater Br/Cl ratio; (2) a lower salinity pore fluid (?5 wt.% NaCl equiv.) with moderately elevated Br/Cl and I/Cl; and (3) fluids with Br/Cl ratios of ～5 times seawater and extremely elevated I/Cl ratios of ～11,500 times seawater. The first two fluids have 40Ar/36Ar of 300–400 and greater than air saturated water 36Ar concentrations that are typical of fluid inclusions related to Zn–Pb mineralisation. The third ‘organic-rich’ fluid has the highest 40Ar/36Ar ratio of up to 1500 and a depleted 36Ar concentration.Mineralisation is interpreted to have resulted from mixing of Zn-rich evaporitic brines and H2S present in hydrocarbons. It is suggested that aqueous fluids acquired organic Br and I from hydrocarbons, and that hydrocarbons exsolving from the aqueous fluid removed noble gases from solution. Interaction of variably saline brines and hydrocarbons could account for the variable Br/Cl and I/Cl composition, and 36Ar concentrations, recorded by Lennard Shelf fluid inclusions. The distinct 40Ar/36Ar signature of the fluid with the highest I/Cl ratio suggests the hydrocarbons and brines were sourced independently from different parts of the sedimentary basin. These data indicate the complementary nature of halogen and noble gas analysis and provide new constraints on important mixing processes during sediment-hosted Zn–Pb mineralisation.  相似文献   

13.
The formation of natural cryogenic brines   总被引：1，自引：0，他引：1  
The source of salts in the Ca-chloridic, hypersaline brines (up to 190 g Cl L−1) occurring in crystalline basement rocks in the Canadian, Fennoscandian and Bohemian Shields and their evolution have been investigated and reported. The Cl-Br-Na relationship indicates that these waters have been concentrated from seawater, by freezing during glacial times. The Na/Cl ratio (0.25 to 0.35) in the more saline fluids is compatible with cooling down to −30°C, where the most saline waters have been concentrated by a factor of 25 to 30 relative to the parent seawater.The brines formed from seawater within cryogenic troughs, along the subarctic continental margins, around ice sheets. The depressions within which the brines formed are the cryogenic analogues of the classic, evaporitic lagoon. One million years suffice to saturate with brine a 2000km-radius by 1km-depth rock volume at an H2O removal rate of only 2.8 mm/yr. Density-induced brine migration on a continental scale takes place via fissures below the ice.Our calculations, that were performed on a hypothetical ice sheet with dimensions compatible with the Laurentide ice sheet, demonstrate that during 1m.y., a 60m thick cryogenic sediment section could have formed. However, the precipitated minerals (mirabilite and hydrohalite) are repeatedly dispersed by the advance and retreat of the ice sheet, dissolved by melt water-seawater mixtures, and eroded during postglacial uplift, leaving almost no trace in the geological record.The cryogenic brines formed intermittently during and between glacial periods. The repeating advance and retreat of the ice sheets exerted a major control on the direction and intensity of brine flow. The cryogenic concentration of seawater and the migration of brine towards the center of the glaciostatic depression occurred mainly during the build up of the ice sheet, while reversal of the water flow from the center of the cryogenic basin outwards happened upon deglaciation. The flow of the waters in the subsurface was, inevitably, accompanied by significant dilution with melt water from the ice sheets.Using a “granitic” U concentration of 4 ppm and a (Ca-Mg mass balance based) rock/water ratio anywhere between 3.4 and 6.8 kg L−1, a few hundred thousand years of brine-rock interaction are sufficient for the growth of 129I in the most saline Canadian Shield brine to its present concentration (3.4×108 atoms 129I L−1). Hence, both the formation of the saline fluids and their emplacement in their present sites occurred most likely within the Pleistocene.The young age calculated for cryogenic brines in crystalline shields and the dynamic water flow therein should raise concern about the planning and construction of high-grade nuclear waste repositories in such rocks, which are already under way.  相似文献   

14.
High-salinity, Na–Ca–Cl-rich fluids (˜20 wt% salts) in inclusions in gangue and ore minerals from Mesozoic Mississippi Valley-type (MVT) deposits in the Verviers Synclinorium (eastern Belgium) and in Cretaceous vein calcites at the Variscan front were investigated by microthermometric and crush-leach analysis. The MVT deposits formed at temperatures of ˜110 °C while the Cretaceous vein calcites were precipitated at temperatures <50 °C. Their Cl–Br content (Cl/Br ratio between 246 and 458) suggests that the fluids probably originated by the evaporation of seawater during basin development at the southern margin of the Caledonian Brabant Massif in the Late Palaeozoic. The Na–Ca–K content (Na: 29,700–49,600 ppm, Ca: 25,700–46,200 ppm, K: 1,000–5,620 ppm) is similar to that of the mineralising fluids in other Pb–Zn districts, interpreted to be of evaporative origin (e.g. Newfoundland, East Tennessee, Polaris). Furthermore, comparison of the Na–Ca–K content of the fluids with that of an evolved evaporitic brine enables the recognition of major water–rock interactions that modified the fluid composition. It indicates that the ambient fluids participated in the early diagenetic dolomitisation of Upper Palaeozoic carbonates and also in the albitisation of plagioclase in Lower Palaeozoic siliciclastics of the Caledonian basement. Illitisation of smectites or dissolution of K-feldspar probably controlled the K-content of the fluids. A model is proposed where the bittern brines migrated down into the deep subsurface because of their density during extension. After the Variscan orogeny, these fluids were finally expelled along extensional faults, resulting in the formation of Zn–Pb deposits. Received: 26 April 2000 / Accepted: 22 November 2000  相似文献   

15.
The central trough of the Bolivian Altiplano is occupied by two wide salt crusts: the salar of Uyuni, which is probably the largest salt pan in the world (10,000 km2) and the salar of Coipasa (2,500 km2). Both crusts are essentially made of porous halite filled with an interstitial brine very rich in Li, K, Mg, B (up to 4.7 g/l Li, 4.3 g/l B, 30 g/l K and 75 g/l Mg). Lithium reserves are the highest known in the world, around 9 × 106 tons. Potassium, magnesium and boron reserves in brines are also important (around 194 × 106 tons K, 8 × 106 tons B and 211 × 106 tons Mg).

The crusts are the remnant of saline Lake Tauca (13,000–10,000 yr BP). Its salinity was estimated approximately at 80 g/l. Its paleochemistry was derived in two ways: (1) by dissolving the present amounts of all chemical components in the former lake volume, and (2) by simulating the evaporation of the major inflows to the basin. The resulting chemical compositions are quite different. The dissolution-derived one is 5 to 50 times less concentrated in Li, K, Mg, B than the evaporation-simulated ones. However all compositions present the same Na and Cl contents. This suggests either a removal of bittern salts or an enrichment of the former lake water in Na and Cl.

The most probable interpretation is that Lake Tauca redissolved a salt crust akin to that existing today. Several older lakes have been detected on the Altiplano. Nevertheless, such an explanation only pushes the problem back. It is likely that the anomaly was transferred from one lake to an other. Three hypotheses may be put forward: (1) bittern seepage through bottom sediments, (2) uptake of the missing components by minerals, and (3) leaching of ancient evaporites from the catchment area at the beginning of the lacustrine history of the basin. The excess halite could have been recycled from lake to lake. This latter process seems to be the most effective to explain the large excess of Na and Cl over the bittern solutes — Li, K, Mg and B. The occurrence of almost pure Na/1bCl saline springs flowing out from a gypsum diapir in the northern Altiplano gives substantial support to this hypothesis.  相似文献   


16.
Seawater at different stages of evaporation from the salt works of Seovlje near Portoro (Yugoslavia) was analyzed geochemically. The seawater there passes through 20 stages of concentration until the first halite crystallizes. All important parameters were determined at all stages: concentrations of Cl, SO4, Na, K, Ca, Mg, and Br, temperature, pH, Eh, oxygen content and titration alkalinity. With increasing evaporation calcium carbonate crystallizes first followed by calcium sulphate as gypsum and after these halite. All three components crystallize from supersaturated solutions. The pH of the initial seawater is 8.32; it falls abruptly to 6.65 when the first calcium carbonate precipitates. Eh in the original seawater is +393 mv; negative values were found in the halite crystallization pans, which contain an anaerobic mud as a reducing agent. The oxygen content of the solution decreases parallel to the drop in Eh. In the pans in which NaCl crystallizes Eh is zero. Apparently the mud also adsorbs K, as can be inferred from a change in the Mg/K ratio.The bromine partition between crystallizing halite and the brine in the salt pans of Seovlje is discussed with regard to some genetic problems of marine salt deposits. In the conditions in the salt pans the bromine partition coefficient at the beginning of NaCl crystallization from seawater—expressed as b=wt.-% Br (mineral)/wt.-% Br (solution)—is 0.12 to 0.14 or—expressed as D=Br/Cl(mineral)/Br/Cl(solution)—0.030 to 0.034 at temperatures between 33° C and 42° C. The conclusion is that a Br content of about 60 to 75 ppm is to be expected for the first halite that crystallizes from evaporating seawater.  相似文献   

17.
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   

18.
Most sedimentary basins contain saline pore water. Saline formation waters can form during burial diagenesis as the result of normal processes of water/rock interaction involving incongruent halite dissolution, bittern salt destruction, and albitization of detrital plagioclase. The kinds of Na-Ca-Cl saline formation waters typical of sedimentary basins can also result from modification of surficial brines formed by the precipitation of NaCl from evaporated seawater. As the porosity of rocks is reduced during burial, discharge of saline formation waters contributes to crustal chloride cycling, and helps explain riverine chloride loads. During burial, the dissolution of metastable detrital minerals derived from crustal rocks in corrosive, saline water transfers incompatible elements such as Li and B from the igneous crust to the sedimentary crust. Similarly, albitization transfers Ca from the crustal silicate (igneous) mineral reservoir to the crustal carbonate and aqueous (sedimentary) reservoirs. Metamorphism and then melting of albite-enriched rocks accounts for the elevated sodium contents of igneous rocks relative to sedimentary rocks. In this way average sediments have become enriched through time in Ca, Cl, Br, S, Li, and B, and depleted in Na relative to average igneous crust.  相似文献   

19.
The Kangan Permo-Triassic brine aquifer and the overlying gas reservoir in the southern Iran are located in Kangan and Dalan Formations, consisting dominantly of limestone, dolomite, and to a lesser extent, shale and anhydrite. The gasfield, 2,900 m in depth and is exploited by 36 wells, some of which produce high salinity water. The produced water gradually changed from fresh to saline, causing severe corrosion in the pipelines and well head facilities. The present research aims to identify the origin of this saline water (brine), as a vital step to manage saline water issues. The major and minor ions, as well as δ2H, δ18O and δ37Cl isotopes were measured in the Kangan aquifer water and/or the saline produced waters. The potential processes causing salinity can be halite dissolution, membrane filtration, and evaporation of water. The potential sources of water may be meteoric, present or paleo-seawater. The Na/Cl and I/Cl ratios versus Cl? concentration preclude halite dissolution. Concentrations of Cl, Na, and total dissolved solid were compared with Br concentration, indicating that the evaporated ancient seawater trapped in the structure is the cause of salinization. δ18O isotope enrichment in the Kangan aquifer water is due to both seawater evaporation and interaction with carbonate rocks. The δ37Cl isotope content also supports the idea of evaporated ancient seawater as the origin of salinity. Membrane filtration is rejected as a possible source of salinity based on the hydrochemistry data, the δ18O value, and incapability of this process to dramatically enhance salinity up to the observed value of 330,000 mg/L. The overlaying impermeable formations, high pressure in the gas reservoir, and the presence of a cap rock above the Kangan gasfield, all prevent the downward flow of meteoric and Persian Gulf waters into the Kangan aquifer. The evaporated ancient seawater is autochthonous, because the Kangan brine aquifer was formed by entrapment of brine seawater during the deposition of carbonates, gypsum, and minor clastic rocks in a lagoon and sabkha environment. The reliability of determining the source of salinity in a deep complicated inaccessible high-pressure aquifer can be improved by combining various methods of hydrochemistry, isotope, hydrodynamics, hydrogeology and geological settings.  相似文献   

20.
Cation and anion concentrations and boron isotopic ratio of brines in the Mishrif Formation (U. Campanian-Tuoronian) from North Rumaila, South Rumaila, Majnoon, Zubair, and West Qurna oilfields southern Iraq were investigated. The aims of this study are to define the type, origin of the oilfield waters, and its flow model in the subsurface oil traps. Mishrif brines are characterized by having higher concentrations of sodium (50,500–84,200 ppm), chlorine (102,100–161,500 ppm), and boron (21.9–31.1 ppm) with lower sulfate contents (187–1350 ppm) relative to the modern seawater. Samples have slightly depleted in δ 11B (35.4‰) relative to seawater fall near the seawater intrusion of the diagram Cl/Br Vs δ 11B and occupied the field of evaporated seawater on the diagrams of Cl vs B and 1/Br vs δ 11B. The brine of Na-chloride type is characteristics of the Mishrif reservoir in all oilfields except WQ which defined by facies of Na-Ca-chloride type. A weak acidic brine of a salinity six-time greater than seawater plays a role in generating the formation pressure and controlling the fluid flow. The reservoir rock-fluid interactions were interpreted using boron isotopes which eventually reveal an ongoing dilution process by the present seawater intrusion and injection water used for the secondary production under conditions of high-temperature digenetic reactions. The 11B in the oilfield water is resulted from uptake of the tetrahedral borate after precipitation of calcium carbonate, while 10B is sourced from the thermal maturation of organic matters.  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