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1.
中国盐湖锂资源及其开发进程   总被引：21，自引：1，他引：21       下载免费PDF全文
赵元艺 《矿床地质》2003,22(1):99-106
锂资源主要分为盐湖型和花岗伟晶岩型两种。文章在作者多年从事有关研究工作的基础上，参阅大量文献，简要介绍了我国盐湖锂资源产出的地质，地理特征与相关主要盐湖锂资源的开发进程，指出我国有丰富的盐湖锂资源，近年来随着提取技术近于成熟，扎布耶盐湖已有具市场竞争的开发技术框架，相关的方法亦趋于成熟，具有变经济优势的前景；班戈湖－杜佳里湖区锂资源提取技术的研究刚刚开发，但已显良好势头，东台吉乃尔湖锂资源的提取技术需完善及改善，西藏扎仓茶卡和鄂雅错－比洛错锂资源提取技术正处于探索之中，最后提出了对我国盐湖锂资源开发的三点建议。  相似文献   

2.
This paper gives an account of the implementation of hydrochemical and isotopic techniques to identify and explain the processes that govern solute exchange in two groundwater-dependent shallow lakes in the Southeastern Pampa Plain of Argentina. Water samples (lakes, streams, spring water and groundwater) for hydrochemical and stable isotopic determination were collected and the main physical–chemical parameters were measured. The combination of stable isotope data with hydrogeochemical techniques was used for the identification of sources and preferential recharge areas to these aquatic ecosystems which allowed the explanation of the lake water origin. The hydrochemical processes which explain Los Padres Lake water chemistry are evaporation from groundwater, CO2 input, calcite dissolution, Na+ release by Ca2+ and Mg2+ exchange, and sulfate reduction. The model that best aligns with La Brava Lake hydrochemical constraints includes: mixing, CO2 and calcite dissolution, cationic exchange with Na+ release and Mg2+ adsorption, and to a lesser extent, Ca/Na exchange. This model suggests that the fractured aquifer contribution to this water body is greater than 50 %. An isotopic-specific fingerprint for each lake was identified, finding a higher evaporation rate for La Brava Lake compared to Los Padres Lake. Isotopic data demonstrate the importance of these shallow lakes as recharge areas to the regional aquifer, becoming areas of high groundwater vulnerability. The Tandilia Range System, considered in many hydrogeological studies as the impermeable bedrock of the Pampean aquifer, acts as a fissured aquifer in this area, contributing to low salinity waters and with a fingerprint similar to groundwater isotopic composition.  相似文献   

3.
The lithium isotopic composition of waters of the Mono Basin, California   总被引：2，自引：0，他引：2  
Mono Lake, a major closed-basin alkaline salt lake in eastern California, derives its water from a mixture of creeks and springs, with the former providing in excess of 75% of the total. The Li isotopic composition of lake water has not varied significantly over a 4 year meromictic period (δ7Li ∼ +19.5). Springs are isotopically distinct: groundwater springs and seeps carry water enriched in isotopically heavy Li whereas thermal springs supply isotopically light (δ7Li < lake), but 10 times more Li-rich, water. Isotopic fractionation during crystallization of carbonate tufa and evaporitic salt appears to be insignificant, and thus cannot be called on as a principal control of the isotopic balance of Li of the lake. Isotopic differences between the end-member source components permit a water budget to be calculated, suggesting (1) springs provide > 50% of the Li to the lake; (2) the Li budget is sensitively balanced on small thermal spring contributions, < 3% of the total spring inflow; and (3) the residence time of Li in the lake is 28 ka. Other Great Basin closed lakes have variable Li isotopic compositions (δ7Li from +16.7 to +23.7), all of which differ significantly from those of several major lakes and seawater (homogeneously ∼ +32).  相似文献   

4.
Chemistry of major and minor elements, 87Sr/86Sr, δD, δ18O and δ34S of brines were measured from Tertiary strata and Quaternary salt lakes in the western Qaidam Basin. The water chemistry data show that all oilfield brines are CaCl2 type. They were enriched in Ca2+, B3+, Li+, Sr2+, Br−, and were depleted in Mg2+, SO4 2−, which indicated that these brines had the characteristics of deeply circulated water. The relationship between δD and δ18O shows that all data of these brines decline towards the Global Meteoric Water Line (GWL) and Qaidam Meteoric Water Line (QWL), and that the intersection between oilfield brines and Meteoric Water Lines was close to the local spring and fresh water in the piedmont in the western Qaidam Basin. The results suggest that oilfield brines has initially originated from meteoric water, and then might be affected by water-rock metamorphose, because most oilfield brines distribute in the range of metamorphosing water. The 87Sr/86Sr values of most oilfield brines range from 0.71121 to 0.71194, and was less than that in salt lake water (>0.712), but close to that of halite in the study area. These imply that salt dissolution occurred in the process of migration. In addition, all oilfield brines have obviously much positive δ34S values (ranging from 26.46‰ to 54.57‰) than that of salt lake brines, which was caused by bacterial sulfate reduction resulting in positive shift of δ34S value and depleteed SO4 2− in oilfield brines. Combined with water chemical data and δD, δ18O, 87Sr/86Sr, δ34S values, we concluded that oilfield brines mainly originate from the deeply circulated meteoric waters, and then are affected by salt dissolution, water-rock metamorphose, sulfate reduction and dolomitization during the process of migration. These processes alter the chemical compositions of oilfield brines and accumulate rich elements (such as B, Li, Sr, Br, K and so on) for sustainable utilization of salt lake resources in the Qaidam Basin.  相似文献   

5.
硫酸钠亚型富锂卤水25℃等温蒸发过程的计算机模拟   总被引：5，自引：0，他引：5  
卜令忠  乜贞  宋彭生 《地质学报》2010,84(11):1708-1714
我国青藏高原上分布有许多盐湖,其中扎布耶等碳酸盐型盐湖、东台吉乃尔等硫酸镁亚型盐湖是著名的富锂盐湖,已成功开发生产出碳酸锂产品。青藏高原上还有许多硫酸钠亚型盐湖,其卤水锂浓度高,钾、镁、硼等有用成分丰富。针对这些盐湖资源,目前尚未进行开发利用研究。这些卤水的等温蒸发实验研究,是必不可少的关键工作之一。本文使用我们由Pitzer电解质溶液理论建立的Li+,Na+,K+,Mg2+/Cl-,SO24--H2O体系的热力学模型,对25℃下几种硫酸钠亚型富锂卤水等温蒸发过程进行了计算机模拟,预测蒸发过程中盐类矿物的析出顺序、卤水组成变化规律、钠、钾、镁、锂盐的饱和点,并在此基础上进行卤水蒸发过程物料平衡关系的理论计算等。本文对西藏3种硫酸钠亚型卤水和国外2种硫酸钠亚型卤水25℃等温蒸发过程进行了模拟。其析盐顺序的特点是:在第一个矿物石盐饱和析出后,接着析出的含钾矿物是钾芒硝,而不是钾镁矾类矿物。其后钾盐则会以钾岩盐形式析出。锂盐饱和后则主要以复盐Li2SO4.K2SO4形式析出。美国银峰卤水的模拟结果与实验蒸发过程完全一致,并给出其继续蒸发时的析盐状况。另4种硫酸钠亚型卤水的模拟结果不仅可以作为未来实验研究的基本参考和注意点,同样也可作为其盐田设计和工艺安排的基本理论依据。本文研究为该类型卤水资源综合开发利用工艺路线的确立提供理论参考。  相似文献   

6.
苦水湖是近年来在青藏高原西昆仑山腹地新发现的富锂盐湖,查明其水化学组成特征对丰富青藏高原盐湖型锂矿床基础资料具有重要的现实意义.然而受区域自然地理条件限制,对包含该盐湖卤水及补给水系的基础性研究还很少.综合运用Piper三线图、Gibbs图解和离子比例关系分析方法探讨了湖表卤水及湖周补给水系水化学组成、演化及主要离子来源.结果表明,由"补给源"到"汇",各离子组成发生了显著变化,水化学类型由碳酸钙镁型向硫酸钠亚型过渡转变,水化学的演化由岩石风化控制向蒸发结晶控制演变.根据离子比例关系,识别出3个主要离子来源:东北径流补给以碳酸盐岩、硅酸岩风化溶质来源为主;南部甜水海水系以盐岩溶解补给为主;湖周冷泉中的溶质则可能主要来自于同生沉积卤水与浅层地下水混合,或长英质火山岩、碳酸盐岩等的深部水-岩作用淋滤.   相似文献   

7.
Progress and Prospects of Salt Lake Research in China   总被引：3，自引：0，他引：3  
China has unique salt lake resources, and they are distributed in the east of Eurasian salt lake subzone of the Northern Hemisphere Salt Lake Zone, mainly concentrated in the regions with modern mean annual precipitation lower than 500 mm. This paper preliminarily reviews the progress made in salt lake research in China for the past 60 years. In the research of Paleoclimate and paleoenvironment from salt lake sediments, a series of salts have been proposed to be indicators of paleoclimate, and have been well accepted by scholars. The chloride-sulfate depositional regions of the west Qaidam and the east Tarim have been revealed to be the drought center of China since the Quaternary, and more than 6 spreading stages of arid climate(salt forming) have been identified. Five pan-lake periods with highstands have been proved to exist during the late Quaternary on the Tibetan Plateau. In mineral resource prospecting and theories of the forming of salt deposits: the atlas(1:2500000) of hydrochemical zoning of salt lakes on the Tibetan Plateau has been compiled for the first time, revealing the zonal distribution and transition from carbonate type to chloride type from south to north and presenting corresponding mineral assemblages for different type of salt lakes; several large continental salt deposits have been discovered and the theory of continental potash deposition has been developed, including the salt deposition in deep basins surrounded by high mountains, the mineral deposition from multistage evolution through chains of moderate or shallow lakes with multilevels, the origin of potassium rich brines in gravel layers, and the forming of potassium deposits through the inheriting from ancient salt deposits, thus establishing the framework of "Continental Potash Deposition Theory"; several new types of Mg-borate deposits have been discovered, including the ulexite and pinnoite bed in Da Qaidam Lake, Qinghai, the pinnoite and kurnakovite bed in Chagcam Caka, Tibet, the kurnakovite bed in Lake Nyer, and the corresponding model of borate deposition from the cooling and dissolution of boron rich brines was proposed based on principles of geology, physics and chemistry. The anti-floatation-cold crystallization method developed independently has improved the capacity of KCl production to 3 million tons per year for the Qarham, serving the famous brand of potash fertilizer products. One 1.2 million ton K-sulfate production line, the biggest in the world, has been built in Lop Nor, and K-sulfate of about 1.6 million tons was produced in 2015. Supported by the new technology, i.e. brine preparation in winter-cooling-solarization-isolation-lithium deposition from salt gradient solar pond" the highest lithium production base at Zabuye Lake(4421 m), Tibet, has been established, which is the first lithium production base in China that reaches the year production of 5000 tons of lithium carbonate. The concept of Salt lake agriculture(Salt land agriculture) has been established based on the mass growth of Dunaliella and other bacillus-algae and the occurrence of various halophytes in saltmarsh and salt saline-alkali lands, finding a new way to increase arable lands and develop related green industry in salt rich environments. Finally this paper presents some new thoughts for the further research and development on salt science, and the further progress in salt science and technology will facilitate the maturing of the interdisciplinary science "Salinology".  相似文献   

8.
Geochemical studies of the ecosystems of 184 Siberian lakes in three largest zones of northern Asia (humid, arid, and semiarid) and in mountainous area were carried out. The contents of natural radionuclides, radiocesium, and rare-earth elements in conjugate components of the systems and the types of the main sources of the bottom sediment material have been determined.Dating of the bottom sediments was made by the activity of radioisotopes 137Cs and 210Pb, which permitted estimation of the sedimentation rates in lakes in different regions of Siberia: 0.35 cm/year in the south and 0.25–0.3 cm/year in the north.Six main ions have been determined in the waters of the studied lakes: Ca2+, Mg2+, Na+, HCO3?, SO42?, and Cl?. The distribution of natural radionuclides in the stratified sections of bottom sediments of Siberian lakes evidences the stable sedimentation and characterizes their contents in the soils of water-catchment areas, which can be considered background contents there. Sediments enriched in organic matter have higher concentrations of U and lower ones of Th and K. The Th/K ratio in the studied bottom sediments is the same as in the soils. The Th/U ratios are somewhat lower than those in the soils because U is accumulated by chemogenic and organic components. The overall 137Cs pollution of bottom sediments of Siberian lakes is close to the global background (40 mCi /km2 in 2000), but in the Altai Territory and Buryatia and Altai Republics it is twice higher. The uneven areal and temporal distribution of residual radiocesium is observed not only in the lacustrine sediments but also in the lake water areas. The REE patterns of bottom sediments of different mineral types are similar to those of continental crust and clays of the Russian Platform, though organogenic and carbonate sediments have higher absolute REE contents than terrigenous ones. Pelitic fraction is the main REE concentrator in the bottom sediments.  相似文献   

9.
Groundwater from karst subterranean streams is among the world’s most important sources of drinking water supplies, and the hydrochemical characteristics of karst water are affected by both natural environment and people. Therefore, the study of karst groundwater hydrochemistry and its solutes’ sources is very important to ensure the normal function of life support systems. This paper focused on the major ion chemistry and sulfate isotope of karst groundwater in Chongqing for tracing the sulfate sources and related hydrochemical processes. Hydrochemical types of karst groundwater in Chongqing were mainly of the Ca-HCO3 type or Ca(Mg)-HCO3 type. However, some hydrochemical types were the K + Na + Ca-SO4 type (G25 site) or Ca-HCO3 + SO4 type (G26 and G14 sites), indicating that the hydrochemistry of these sites may be strongly influenced by anthropogenic activities or unique geological characteristics. The δ34S-SO4 2? of collected karst groundwater sample fell into a range of ?6.8 to 21.5 ‰, with a mean value of 5.6 ‰. In dolomite aquifer, the δ34S-SO4 2? value ranges from ?4.3 to 11.0 ‰, and in limestone aquifer, it ranged from ?6.8 to 21.5 ‰. The groundwater samples from different land use types showed distinctive δ34S-SO4 2? value. The δ34S-SO4 2? value of groundwater samples had range of ?6.8 to 16.7 ‰ (mean 4.0 ‰, n = 11) in cultivated land areas, 1.5–21.5 ‰ (mean 7.2 ‰, n = 20) in forested land areas, and ?4.3 to 0.8 ‰ (mean ?1.7 ‰, n = 2) in coalmine areas. The δ34S-SO4 2? values of groundwater samples collected from factory area and town area were 2.2 and 9.9 ‰, respectively. According to the δ34S information of potential sulfate sources, this paper discussed the possible sulfate sources of collected karst groundwater samples in Chongqing. The variations of both δ34S and 1/SO4 2? values of the groundwater samples indicated that the atmospheric acid deposition (AAD), dissolution of gypsum (GD), oxidation of sulfide mineral (OS) or anthropogenic inputs (SF: sewage or fertilizer) contributed to sulfate in karst groundwater. The influence of oxidation of sulfide mineral, atmospheric acid deposit and anthropogenic inputs to groundwater in Chongqing karst areas was much widespread. For protecting, sustaining, and utilizing the groundwater resources, the sewage possibly originating from urban, mine or industrial area must be controlled and treated, and the use of fertilizer should be limited.  相似文献   

10.
The hydrochemical and multivariate statistical techniques such as the principal component analysis (PCA) and the cluster analysis (CA) were used to identify the hydrochemical processes and their relation with groundwater quality and also to get an insight into the hydrochemical Zana aquifer groundwater chemistry evaluation. Twenty-four samples during the wet season and even during the dry season are analyzed. The Piper diagram showed that water facies are magnesium bicarbonate on the sides of the western reliefs and magnesium chloride-sulfated at the north and the center of the plain. The PCA carried out on three factors revealed that on the factorial design F1-F3, nitrates negatively determine factor 3, indicating the presence of an agriculture pollution. On the factorial design F1-F2, HCO3? positively determine the factor 2, indicating the carbonated origin. However, the CA, based on variables, showed that the waters in the region can be classified into three groups according to flow direction while the CA, based on major ion contents, defined three groups, reflecting the same hydrochemical facies. The first group with dry residue varying between 360 and 1700 mg/l and characterized by Mg2+ and Cl?, HCO3?. Samples of this group are mostly located in the north and northeastern part of the region. The second group with highest dry residue (2080 to 3820 mg/l) characterized by Mg2+ and SO4?, Cl? is located near the Northwestern and western outcrops. The third group coincides with the central part, the lowest of the plain, with heightened dry residue (4140 to 13,950 mg/l), characterized by Mg2+ and SO4?. The hydrochemical study made it possible to allot the evaporitic origin to the elements Na+, Mg2+, K+, Cl?, and SO4?, while for element HCO3?, it results from the carbonated formations. These results showed that the presence of nitrates in the studied area is closely linked to the agricultural activity.  相似文献   

11.
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   

12.
This paper gives an account of the assessment and quantification of the water balance and the hydrogeological processes related to lake–groundwater interaction in the Pampa Plain by using hydrogeochemical, isotopic and flow numerical modeling techniques. La Salada is a permanent shallow lake, with an area of 5.8 km2, located on the SE of Buenos Aires Province. A total of 29 lake water samples and 15 groundwater samples were collected for both hydrochemical analysis and environmental stable isotope determination. Water table depths were measured in wells closed to the lake. Groundwater samples appear grouped on the Local Meteoric Water Line, suggesting a well-mixed system and that rainfall is the main recharge source to the aquifer. Water evaporation process within La Salada is also corroborated by its isotopic composition. The model that best adjusts to La Salada Lake hydrochemical processes includes evaporation from groundwater, calcite precipitation with CO2 release and cationic exchange. The annual water balance terms for the lake basin indicates for each hydrological component the following values: 1.16 E08 m3 rainfall, 8.15 E07 m3 evapotranspiration, 1.90 E06 m3 runoff, 1.55 E07 m3 groundwater recharge, 6.01 E06 m3 groundwater discharge to the lake, 9.54 E06 m3 groundwater discharge to the river, 5.00 E05 m3 urban extraction and 4.90 E06 m3 lake evaporation. Integrated analysis of hydrochemical and isotopic information helped to calibrate the groundwater flow model, to validate the conceptual model and to quantitatively assess the basin water balance.  相似文献   

13.
郑浩  赵海香  谭红兵 《矿床地质》2023,42(2):411-424
麻米错盐湖是西藏境内发育的特大型锂矿床之一,目前对该盐湖的Li、B来源仍存在一定争议。文章系统采集麻米错盐湖水及周边补给水体样品,分析其主量元素特征,并使用多种水化学手段进行讨论,同时对盐湖水、河水及地热水进行蒸发模拟。结果表明,研究区河水及泉水中的主要离子受控于流域内岩石风化作用,其中碳酸盐岩矿物与蒸发岩矿物贡献最大,其次是硅酸盐矿物。文章对补给水体输入盐湖的Li、B资源进行定量计算,得出单纯通过河水和泉水的输入无法形成盐湖目前的探明储量。选择西藏地区最为富Li的地热水同补给水体按照一定比例混合后进行蒸发模拟,发现其析盐序列与盐湖水的析盐序列存在很大程度上的重叠,以上均证明麻米错盐湖中的Li、B资源除受到周边河水及泉水的补给外,还受到地热水的补给。  相似文献   

14.
Saline, 450-m-deep Lake Van (Eastern Anatolia, Turkey) is, with 576 km3, the third largest closed lake on Earth and its largest soda lake. In 1989 and 1990, we investigated the hydrochemistry of the lake’s water column and of the tributary rivers. We also cored the Postglacial sediment column at various water depths. The sediment is varved throughout, allowing precise dating back to ca. 15 ka BP. Furthermore, lake terrace sediments provided a 606-year-long floating chronology of the Glacial high-stand of the lake dating to 21 cal. ka BP. The sediments were investigated for their general mineralogical composition, important geochemical parameters, and pore water chemistry as well. These data allow reconstructing the history of the lake level that has seen several regressions and transgressions since the high-stand at the end of the Last Glacial Maximum. Today, the lake is very alkaline, highly supersaturated with Ca-carbonate and has a salt content of about 22 g kg?1. In summer, the warmer epilimnion is diluted with river water and forms a stable surface layer. Depth of winter mixing differs from year to year but during time of investigation the lake was oxygenated down to its bottom. In general, the lake is characterized by an Na–CO3–Cl–(SO4)-chemistry that evolved from the continuous loss of calcium as carbonate and magnesium in the form of Mg-silica-rich mineral phases. The Mg cycle is closely related to that of silica which in turn is governed by the production and dissolution of diatoms as the dominant phytoplankton species in Lake Van. In addition to Ca and Mg, a mass balance approach based on the recent lake chemistry and river influx suggests a fractional loss of potassium, sodium, sulfur, and carbon in comparison to chloride in the compositional history of Lake Van. Within the last 3 ka, minor lake level changes seem to control the frequency of deep water renewal, the depth of stratification, and the redox state of the hypolimnion. Former major regressions are marked by Mg-carbonate occurrences in the otherwise Ca-carbonate dominated sediment record. Pore water data suggest that, subsequent to the major regression culminating at 10.7 ka BP, a brine layer formed in the deep basin that existed for about 7 ka. Final overturn of the lake, triggered by the last major regression starting at about 3.5 ka BP, may partly account for the relative depletion in sulfur and carbon due to rapid loss of accumulated gases. An even stronger desiccation phase is proposed for the time span between about 20 and 15 ka BP following the LGM, during which major salts could have been lost by precipitation of Na-carbonates and Na-sulfates.  相似文献   

15.
Soils, rocks, altered rocks, hot and cold waters, and hot spring precipitates were sampled within and on the outskirts of geothermal fields in China. The contents of thirty trace elements in soils and rocks show that Hg, As, Sb, Bi, Li, Rb, Cs, Au, Ag, B, W, Sn, Pb, Zn, Mn, Ni and Co can serve as direct and indirect indicators for geothermal field exploration. Large amounts of data indicate that Hg, As and Sb are the best indicators of hot water sources. Altered rocks contain higher Hg, As, Sb, Bi and Be than unaltered rocks. Based on their abundances in hot waters, it is suggested that the following elements may be used as hydrochemical indicators of high-temperature hot-water geothermal systems: K+, Na+, Ca2+, Mg2+, SO2−4, HCO−3, F−, Cl−, SiO2, HBO2, CO2, pH, total dissolved solids and hydrochemical types, as well as Hg, As, Sb, Be, Li, Rb and Cs. Modern precipitates associated with hot springs have high contents of Ba, Be, Fe, Ti, Hg, As, Sb and Bi. Using these geochemical data, the authors have had much success in locating hot water drill sites within geothermal fields. Case histories are described for five geothermal areas.  相似文献   

16.
The surface sediments of two mud mounds (“Mound 11” and “Mound 12”) offshore southwest Costa Rica contain abundant authigenic carbonate concretions dominated by high-Mg calcite (14–20 mol-% MgCO3). Pore fluid geochemical profiles (sulfate, sulfide, methane, alkalinity, Ca and Mg) indicate recent carbonate precipitation within the zone of anaerobic oxidation of methane (AOM) at variable depths. The current location of the authigenic carbonate concretions is, however, not related to the present location of the AOM zone, suggesting mineral precipitation under past geochemical conditions as well as changes in the flow rates of upward migrating fluids. Stable oxygen and carbon isotope analysis of authigenic carbonate concretions yielded δ18Ocarbonate values ranging between 34.0 and 37.7 ‰ Vienna standard mean ocean water (VSMOW) and δ13Ccarbonate values from ?52.2 to ?14.2 ‰ Vienna Pee Dee belemnite (VPDB). Assuming that no temperature changes occurred during mineral formation, the authigenic carbonate concretions have been formed at in situ temperature of 4–5 °C. The δ18Ocarbonate values suggest mineral formation from seawater-derived pore fluid (δ18Oporefluid = 0 ‰ VSMOW) for Mound 12 carbonate concretions but also the presence of an emanating diagenetic fluid (δ18Oporefluid ≈5 ‰) in Mound 11. A positive correlation between δ13Ccarbonate and δ18Ocarbonate is observed, indicating the admixing of two different sources of dissolved carbon and oxygen in the sediments of the two mounds. The carbon of these sources are (1) marine bicarbonate (δ13Cporefluid ≈0 ‰) and (2) bicarbonate which formed during the AOM (δ13Cporefluid ≈?70 ‰). Furthermore, the δ18Oporefluid composition, with values up to +4.7 ‰ Vienna standard mean ocean water (VSMOW), is interpreted to be affected by the presence of emanating, freshened and boron-enriched fluids. Earlier, it has been shown that the origin of 18O-enriched fluids are deep diagenetic processes as it was indicated by the presence of methane with thermogenic signature (δ13CCH4 = ?38 ‰). A combination of present geochemical data with geophysical observations indicates that Mounds 11 and 12 represent a single fluid system interconnected by deep-seated fault(s).  相似文献   

17.
第四纪盐湖沉积与古气候   总被引：81，自引：9，他引：72       下载免费PDF全文
笔者通过国内第四纪盐湖沉积的长期实地考察以及盐湖长期科学观察站的实验研究,并结合国内外大量盐湖沉积实验研究资料,以比较盐湖沉积学的理论和方法,将盐湖沉积划分为冷相、暖相和广温相,揭示现代全球盐湖水化学类型分带与气候分区的一致性;指出我国第四纪存在6次干旱(成盐)扩张期;识别出中国第四纪干旱中心19个明显的强冷偏湿-冷干事件及8个明显的暖偏湿-暖干事件,并推算其古气温变化范围。  相似文献   

18.
中国盐湖的基本特征   总被引：4，自引：1，他引：4       下载免费PDF全文
陈克造 《第四纪研究》1992,12(3):193-202
盐湖中蕴藏着富饶的非金属和稀土矿产资源,盐湖沉积序列对研究干旱-半干旱区的古气候古环境演变,也占有重要的地位。本文综合现有资料,论述了中国盐湖的分布、水化学特征和盐湖类型、盐类矿物、盐类物质来源以及成盐期的基本特征。  相似文献   

19.
Assessment of groundwater quality in and around Vedaraniyam,South India   总被引：1，自引：1，他引：0  
Groundwater from 47 wells were analyzed on the basis of hydrochemical parameters like pH, electric conductivity, total dissolved solids, Ca2+, Mg2+, Na+, K+, Cl?, CO3 2?, HCO3 ?, NO3 ?, PO4 3? and F? in the Cauvery delta of Vedaraniyam coast. Further, water quality index (WQI), sodium percentage (Na %), sodium absorption ratio, residual sodium carbonate, permeability index and Kelley’s ratio were evaluated to understand the suitability of water for drinking and irrigation purposes. The result shows significant difference in the quality of water along the coastal stretch. The order of dominance of major ions is as follows: Na+ ≥ Mg2+ ≥ Ca2+ ≥ K+ and Cl? ≥ HCO3 ? ≥ CO3 2? ≥ PO4 3? ≥ F?. Na/Cl, Cl/HCO3 ratio and Revelle index confirmed that 60–70 % of the samples were affected by saline water intrusion. WQI showed that 36 % of the samples were good for drinking and the remaining were poor and unsuitable for drinking purpose. The degradation of groundwater quality was found to be mainly due to over-exploitation, brackish aquaculture practice, fertilizer input from agriculture and also due to domestic sewage.  相似文献   

20.
Rare earth element (REE) concentrations in alkaline lakes, circumneutral pH groundwaters, and an acidic freshwater lake were determined along with the free carbonate, free phosphate, and free sulfate ion concentrations. These parameters were used to evaluate the saturation state of these waters with respect to REE phosphate and carbonate precipitates. Our activity product estimates indicate that the alkaline lake waters and groundwaters are approximately saturated with respect to the REE phosphate precipitates but are significantly undersaturated with respect to REE carbonate and sulfate precipitates. On the other hand, the acidic lake waters are undersaturated with respect to REE sulfate, carbonate, and phosphate precipitates. Although carbonate complexes tend to dominate the speciation of the REEs in neutral and alkaline waters, our results indicate that REE phosphate precipitates are also important in controlling REE behavior. More specifically, elevated carbonate ion concentrations in neutral to alkaline natural waters tend to enhance dissolved REE concentrations through the formation of stable REE-carbonate complexes whereas phosphate ions tend to lead to the removal of the REEs from solution in these waters by the formation of REE-phosphate salts. Removal of REEs by precipitation as phosphate phases in the acid lake (pH=3.6) is inconsequential, however, due to extremely low [PO 4 3– ] F concentrations (i.e., 10–23 mol/kg).  相似文献   

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