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1.
Brinck EL  Frost CD 《Ground water》2007,45(5):554-568
Water introduced to surface drainages, such as agricultural and roadway runoff, mine drainage, or coalbed natural gas (CBNG)-produced water, potentially can be of environmental concern. In order to mitigate potential environmental effects, it may be important to be able to trace water discharged to the surface as it infiltrates and interacts with near-surface aquifers. We have chosen to study water withdrawn during CBNG production for isotope tracing in the hyporheic zone because it poses a variety of economic, environmental, and policy issues in the Rocky Mountain states. Ground water quality must be protected as CBNG water is added to semiarid ecosystems. Strontium (Sr) isotopes are effective fingerprints of the aquifer from which water originates. In this study, CBNG water was found to have a higher (87)Sr/(86)Sr ratio than the local alluvial aquifer water. This measurable difference allows the strontium isotope ratio and concentration to be used as tracers of CBNG water following its discharge to the surface. The dissolution and mobilization of salts from soil are an important contributor to ground water quality degradation. In the Powder River basin of Wyoming, the soils are calcium carbonate-buffered systems. The chemical similarity of strontium to calcium allows it to substitute into calcium minerals and enabled us to use strontium isotopes to identify calcium salts mobilized from the soil. Strontium isotopes are an effective monitor of the source of ions and the volume and direction of introduced water flow in the hyporheic zone.  相似文献   

2.
Strontium isotope stratigraphy (SIS) has progressively become an efficient chemostratigraphic tool in the research and correlation of global geological events, such as global sea level fluctuations, orogeny, and paleoclimatic and paleoenvironmental changes. In this paper, 87Sr/86Sr ratios of the Triassic marine carbonate rock samples from Huaying Mountains, eastern Sichuan are measured, and the corre-sponding Sr-isotopic curve is constructed, based on the fundamental principle of strontium isotope stratigraphy, analysis of rock fabric, luminescent intensity, chemical composition and representative evaluation for the coeval seawater information. The 87Sr/86Sr ratios show a rapid rise from 0.70721 near the Permian-Triassic transition to 0.70830 at the end of Early Triassic, and then they decline rapidly to 0.70787 in the early Middle Triassic. These data are generally coincident with 87Sr/86Sr ratios of coeval seawater from previous papers, and the curve is also similar to other previous curves. This indicates that the global geological events are the most important controlling factors to the strontium isotope evolution of the global seawater in the Early and Middle Triassic.  相似文献   

3.
Oceanic87Sr/86Sr ratios during Jurassic to Pleistocene have been determined by analysing fresh waters from marine limestone and dolomite aquifers. The results are in good agreement with published data from well preserved fossil material. The87Sr/86Sr ratios obtained are 0.7070 for Lower to Middle Jurassic, 0.7075 for Late Cretaceous, 0.7080 for Lower to Middle Eocene and 0.7087 for Pleistocene aquifer waters. The value of87Sr/86Sr for the Eimer and Amend isotopic standard was 0.7082.  相似文献   

4.
Analyses of rim-to-interior samples of fresh tholeiitic pillow basalts, deuterically altered holocrystalline basalts, and older, weathered tholeiitic basalts from the deep sea indicate that 87Sr/86Sr ratios of the older basalts are raised by low temperature interaction with strontium dissolved in sea water. 87Sr/86Sr correlates positively with H2O in these basalts; however, there is little detectable modification of the strontium isotope composition in rocks with H2O contents less than 1%. The isotope changes appear to be a function of relatively long-term, low-temperature weathering, rather than high-temperature or deuteric alteration. Strontium abundance and isotopic data for these rocks suggest that strontium content is only slightly modified by interaction with sea water, and it is a relatively insensitive indicator of marine alteration. Average Rb-Sr parameters for samples of apparently unaltered basalt are: Rb= 1.11ppm; Sr= 132ppm; 87Sr/86Sr= 0.70247.  相似文献   

5.
The concentrations and isotopic compositions of strontium in interstitial waters from several DSDP sites, where sediments consist chiefly of carbonate oozes and chalks, are used as indicators of carbonate diagenesis by reference to a recently-produced curve showing detailed variations in the87Sr/86Sr ratio of seawater with time. Carbonate sediments of the Walvis Ridge show increases in interstitial Sr2+ concentrations in the upper carbonate-ooze sections with the highest concentrations near the ooze-chalk boundary where maximum rates of carbonate recrystallization occur. Below this, in situ production of Sr2+ diminishes and there is a diffusive flux of Sr to an underlying sink, presumably volcanogenic sediments or basalts, leading to Sr isotopic disequilibrium between carbonates and interstitial waters. In some other sites, however, there is no apparent Sr sink at depth and isotopic equilibrium is retained. Overall, diffusive smoothing of profiles exerts an important control on the87Sr/86Sr ratios, although lower ratios than contemporaneous seawater values in the carbonate oozes often correlate with zones of Mg2+ loss and reflect a combination of a flux of Sr2+ from the zone of maximum recrystallization rates together with a contribution from the in situ alteration of volcanic matter.  相似文献   

6.
Strontium (Sr) concentrations and isotopic ratios have been measured in a series of water and rock samples from most of the major tributaries of the Lake Qinghai basin on the north‐eastern Tibetan Plateau. Dissolved Sr and 87Sr/86Sr show ranges of 488–12 240 nmol/l and 0·710497–0·716977, respectively. These data, together with measurements of major cations and anions in rivers and their tributaries and various lithologies of the catchment, were used to determine the contributions of Sr and its isotopic expense to rivers and lakes. Our results demonstrate that the chemical components and 87Sr/86Sr ratios of the alkaline waters are derived from mixing of carbonate and silicate sources, with the former contributing 72 ± 18% dissolved Sr to rivers. The difference in tributary compositions stems from the lithology of different river systems and low weathering intensity under a semi‐arid condition. Variation in 87Sr/86Sr ratios places constraint on the Sr‐isotopic compositions of the main tributaries surrounding Lake Qinghai. The water chemistry of the Buha River, the largest river within the catchment underlain by the late Paleozoic marine limestone and sandstones, dominates Sr isotopic composition of the lake water, being buffered by the waters from the other rivers and probably by groundwater. However, the characteristic chemical composition of the lake itself differs remarkably from the rivers, which can be attributed to precipitation of authigenic carbonates (low‐magnesium calcite, aragonite, and dolomite), though this does not impact the Sr isotope signature, which may remain a faithful indicator in paleo‐records. Regarding the potential role of groundwater input within the Lake Qinghai systems in the water budget and water chemistry, we have also determined the Sr concentration and 87Sr/S6Sr ratio of groundwater from diverse environments. This has allowed us to further constrain the Sr isotope systematic of this source. A steady‐state calculation gives an estimate for the groundwater flux of 0·19 ± 0·03 × 108 m3/yr, accounting for about 8% of contemporary lake Sr budget. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

7.
Access to fresh water is one of the major issues of northern and sub-Saharan Africa. The majority of the fresh water used for drinking and irrigation is obtained from large ground water basins where there is minor contemporary recharge and the aquifers cross national borders. These aquifers include the Nubian Aquifer System shared by Chad, Egypt, Libya, and Sudan; the Iullemeden Aquifer System, extending over Niger, Nigeria, Mali, Benin, and Algeria; and the Northwest Sahara Aquifer System shared by Algeria, Libya, and Tunisia. These resources are subject to increased exploitation and may be severely stressed if not managed properly as witnessed already by declining water levels. In order to make appropriate decisions for the sustainable management of these shared water resources, planners and managers in different countries need an improved knowledge base of hydrological information. Three technical cooperation projects related to aquifer systems will be implemented by the International Atomic Energy Agency, in collaboration with the United Nations Educational, Scientific and Cultural Organization and United Nations Development Programme/Global Environmental Facility. These projects focus on isotope hydrology studies to better quantify ground water recharge and dynamics. The multiple isotope approach combining commonly used isotopes 18O and 2H together with more recently developed techniques (chlorofluorocarbons, 36Cl, noble gases) will be applied to improve the conceptual model to study stratification and ground water flows. Moreover, the isotopes will be an important indicator of changes in the aquifer due to water abstraction, and therefore they will assist in the effort to establish a sustainable ground water management.  相似文献   

8.
87Sr/86Sr ratios of marine carbonate samples collected from a sedimentary section of the Late Cretaceous in the south of Tibet were measured. Based on the absence of cathodo-luminescence and a very low Mn/Sr ratio (average 0.06) of the samples, it is thought that they contain information on the original seawater strontium isotope composition. The strontium isotope evolution curve of the Late Cretaceous in Tibet we established here, is consistent with other coeval curves from Europe, North America and Antarctica, supports the notion that the strontium isotope composition of seawater is governed by global events, which provides a new approach for the inter-continental and inter-basinal correlations of Late Cretaceous in the area and is a complementarity for biostratigraphy. In addition, we attempt to determine the age of the boundaries for Campanian/Santonian and Maastrichtian/Campanian by 87Sr/86Sr ratios for Gamba section in southern Tibet. The two boundaries are located in the thickness of 217 m (83.5 M  相似文献   

9.
This study uses Sr isotope composition (87Sr/86Sr) and Sr content of waters of the Oder, one of the largest rivers in central Europe, to fingerprint natural and anthropogenic contributions to its Sr budget and to evaluate water mixing processes in its hydrological system. It also demonstrates a simple method of quantifying natural and anthropogenic Sr inputs in the watershed. The method has potential for environmental and archaeological research because past Sr geochemistry of river water can easily be reconstructed. For the first time, a catchment‐scale impact of anthropogenic sources on the Sr budget of a middle‐size river is shown in a quantitative way. The water of the Oder is characterized by a relatively uniform Sr isotope composition, from 0.7100 to 0.7108, contrasting with strong variations in Sr concentration, from 0.25 to 1.27 mg/L. There is a general seasonal trend in variability, with waters becoming more radiogenic and dilute with respect to the Sr in the spring time. This Sr systematics differs significantly from the Sr budgets of the majority of the Oder tributaries that exhibit more radiogenic composition and systematically lower Sr concentrations. A mixing scenario in the Oder involves Sr contribution from four principal water sources: (a) shallow ground waters with Sr derived from near‐surface weathering of silicates, (b) moderately radiogenic mine waters from the Upper Silesian Coal Basin, (c) unradiogenic mine waters from the Permian sequence of the copper district, and (d) unradiogenic ground waters from shallow‐seated Palaeogene, Neogene, and Mesozoic aquifers. The Sr budget of the Oder is primarily controlled by inputs of dissolved Sr from anthropogenic sources, which overprint the natural background, controlled by geology. Thus, about 47.5% of Sr originates from agriculture, industrial, and municipal additions, 31.5% from mine water inputs, and only 21% from natural sources, that is, rock weathering and atmospheric precipitation. Reconstruction of the past Sr chemistry of the Oder reveals that its present‐day Sr isotope composition is temporary and significantly different from that of the preindustrial times.  相似文献   

10.
In the Ordovician, a carbonate platform system grading from the platformal interior eastwards to basin was developed in the Tazhong area of the Tarim Basin, and the study column is located in the place where the paleoslope occurred. The isotope compositions of the carbonates there are thus considered as having reflected those of simultaneous sea waters in view of its good connection with the open seas. The carbon and strontium isotope compositions of the Ordovician carbonates in the Tazhong area are analyzed, and their relationships to the sea-level fluctuations are discussed as well. Studies have revealed that the carbon isotope composition is related positively with the sea-level fluctuations, whereas an opposing situation occurs to the strontium isotope variation. Similar responses of carbon and strontium isotope compositions to the sea-level fluctuations are reported elsewhere in the world, suggesting that the Ordovician sea-level fluctuations of the Tarim Basin were of eustatic implication.  相似文献   

11.
本文以著名的泥河湾盆地小渡口剖面28层为实例,通过有孔虫,介形虫,腹足类微体生物壳体87Sr/86Sr比值与盆地汇水区域Sr同位素地层分布特征对比分析以及生物壳体Sr/Ca国度的相关性,来重塑沉积盆地汇水来源变更,湖水变化等古水文要素,进而可以反演区域构造－气候变化,实例研究结果表明,生物壳体87Cr/86Sr 及Sr/Ca比值等地球化学方法是恢复盆地古水文条件的重要手段。  相似文献   

12.
The investigation of the regional flow characteristics of aquifers is important with respect to aquifer management. To determine regional flows, use can be made of hydraulic and hydrochemical data. In a study of a Chalk Aquifer System in the south of Lincolnshire, England, a combined hydrochemical approach using major, minor and isotope chemistry is described. The chemical data have been used because hydraulic information is difficult to interpret both locally and regionally as a consequence of multi-layered hydraulic zones, nonhomogeneous fissure zones, and variable erosional features. By characterizing ground-water types on the basis of major ion chemistry, and subsequently interrelating with minor ion distributions (notably iodide supported by strontium), a reasonable assessment of operative flow paths and mechanisms has been made. Substantiation of the conclusions reached using major and minor ion chemistry is provided by the environmental isotope data of carbon and tritium.  相似文献   

13.
The Kaluvelly watershed is a coastal area (Tamil Nadu, India) where water abstraction has resulted in a dramatic fall in the level of the water table and a piezometric depression in the most exploited aquifer, the Vanur aquifer. In addition, intensification/mechanization of agriculture may have affected the quality of recharge water. An initial hydrodynamic study showed that the Vanur aquifer is highly vulnerable to salinization due to potential seawater intrusion, and our aim was to determine the source of salinity recorded in the groundwater of this multilayered aquifer. Our approach involved the use of existing boreholes and of a moderate number of samples, with the aim of developing appropriate water resource management techniques. Major element, 18O/16O, 2H/1H and 87Sr/86Sr, ratios were measured in rainwater, surface water and groundwater collected during five sampling campaigns over a 2‐year period. Geochemical data indicate that the Vanur aquifer is recharged and that small mixings between aquifers fluctuate according to monsoon intensity. There was no evidence of seawater intrusion. The range of recorded salinity originated mainly from water–rock interaction but a disconnection of some deeper parts of the aquifer was apparent. Strontium isotopic ratios in the recharge area suggest an anthropogenic influence, possibly related to fertilizer use. A high SO4/Cl ratio was observed in the aquifer; in the deeper parts, the influence of a formation containing lignite is hypothesized, whereas near the surface, sulphate may partly originate from fertilizer use and fossil fuel combustion. Water isotopic data suggest that the origin of precipitation in this region has been unchanged for several hundreds or thousands of years. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

14.
Carbonate species, dissolved in appreciable quantities in all ground waters, can be extracted and used for radiocarbon dating. The material is mainly of biogenic origin, but contains some bicarbonate produced from limestone. This causes a dilution of the radiocarbon activity of the total carbonate species in the water and a correction is necessary in order to determine absolute radiocarbon ages, i.e., the time since the waters went underground. Three methods of evaluating the limestone contributions are examined critically: carbonate species ratios, carbon-13 variations, and concurrent tritium measurements. All possess uncertainties. The largest errors occur in the carbon-13 procedure, due to the wide natural fluctuation of the stable isotope content in plants and the occurrence of isotope effects in the soil air-water carbon dioxide exchange. Comparisons of the limestone dilution correction techniques show that they produce analogous results in actual aquifer studies, but with small differences in the calculated radiocarbon ages. The reasons for these inconsistencies have not yet been unequivocally established. Two problems are: the possibility of irreversible exchange of the ground water dissolved carbonate species with limestone in the aquifer matrix, and the significance of exchange of carbon dioxide in the water with that of the soil air in the surface layer of the catchment zone. Experiments are suggested that could resolve these questions.  相似文献   

15.
Ground-water levels in the Upper Floridan aquifer beneath the southeastern coast of South Carolina have undergone pumpage-induced declines approaching 20 ft below sea level at the southern end of Hilton Head Island. This scenario suggests the potential exists for the inducement of recharge to the Upper Floridan aquifer across the island, which could affect the quality of water being pumped by wells. However, low radiocarbon concentrations in ground-water samples (0.5 to 1.4 ± 0.1 PMC) indicate that most of the water is relict ground water reflecting prepumpage ground-water flow conditions in the Upper Floridan aquifer. The isotopic data indicate long residence times and water-chemistry evolution more characteristic of ground-water recharge occurring farther inland prior to the commencement of pumpage in the late 1800s. Radiocarbon concentrations (as Percent Modern Carbon) and stable carbon isotope ratios (as δ13C in dissolved inorganic carbon) determined during this study and reported in other studies on and around Hilton Head Island varied in a systematic manner. Heavier δ13C values (–2.8 to –1.6 per mil) in ground water beneath southern Hilton Head Island reflect ground-water discharge from prepumpage flowpaths originating over 100 miles away, hence a depletion in radiocarbon concentration with corrected ground-water ages no younger than 16,000 yrs BP. In contrast, lighter δ13C values (–13.9 to –8.67 per mil) beneath the northern part of the island indicate recent recharge as a result of water-level declines, and recharge in areas off the island that have not changed as a result of pumpage (evidenced by enrichment in radiocarbon with corrected ground-water ages no older than 4,000 yrs BP). This suggests that the δ13C composition of ground water in the Upper Floridan aquifer is a useful indicator of mixing between ground waters from different sources, and can be used to delineate recharge-discharge patterns. This approach may be applicable to other aquifers of highly evolved ground-water chemistry in regional carbonate aquifer systems that may be receiving recent recharge. Moreover, this approach could prove useful in delineating the contribution of recent water being captured by pumped wells as part of wellhead protection programs designed to assess aquifer vulnerability from surficial contaminant sources.  相似文献   

16.
The stable isotope ratios of groundwater sulfate (34S/32S, 18O/16O) are often used as tracers to help determine the origin of groundwater or groundwater contaminants. In agricultural watersheds, little is known about how the increased use of sulfur as a soil amendment to optimize crop production is affecting the isotopic composition of groundwater sulfate, especially in shallow aquifers. We investigated the isotopic composition of synthetic agricultural fertilizers and groundwater sulfate in an area of intensive agricultural activity, in Ontario, Canada. Groundwater samples from an unconfined surficial sand aquifer (Lake Algonquin Sand Aquifer) were analyzed from multi-level monitoring wells, riverbank seeps, and private domestic wells. Fertilizers used in the area were analyzed for sulfur/sulfate content and stable isotopic composition (δ18O and/or δ34S). Fertilizers were isotopically distinct from geological sources of groundwater sulfate in the watershed and groundwater sulfate exhibited a wide range of δ34S (−6.9 to +20.0‰) and δ18O (−5.0 to +13.7‰) values. Quantitative apportionment of sulfate sources based on stable isotope data alone was not possible, largely because two of the potential fertilizer sulfate sources had an isotopic composition on the mixing line between two natural geological sources of sulfate in the aquifer. This study demonstrates that, when sulfate isotope analysis is being used as a tracer or co-tracer of the origin of groundwater or of contaminants in groundwater, sulfate derived from synthetic fertilizer needs to be considered as a potential source, especially when other parameters such as nitrate independently indicate fertilizer impacts to groundwater quality.  相似文献   

17.
Mass balance calculations and hydrodynamics of groundwater flow suggest that the solutes in brines of the coastal sabkha aquifer from the Emirate of Abu Dhabi are derived largely from ascending geologic brines into the sabkha from the underlying formations. Solute interpretation for the ascending brine model (ABM) was based on two independent but secondary lines of evidence (solute ratios and solute fluxes). In the current study, direct primary evidence for this ABM was provided through analyses of δ81Br, δ37Cl, and 87Sr/86Sr. Different solute histories of geologic brine and sea water provide an “isotopic fingerprint” that can uniquely distinguish between the two possible sources. Samples from the coastal sabkha aquifer of Abu Dhabi were determined to have a mean δ81Br of 1.17‰ that is statistically equal, at the 95% confidence level, to the mean of 1.11‰ observed in the underlying geologic brine and statistically different than sea water. Similarly, the δ37Cl in sabkha brine has a mean of 0.25‰ and is statistically equal to a mean of 0.21‰ in the underlying geologic brines at the 95% confidence level and statistically different from sea water. Also, dissolved strontium isotope data are consistent with the ABM and even with the complex set of processes in the sabkha, the variance in strontium isotope results is similar to the geologic brine. These observations provide primary direct evidence consistent that the major source of these solutes (and presumably others in the aquifer) is from discharging geologic brines, not from adjacent sea water.  相似文献   

18.
We report the results of a detailed study of dissolved Sr isotopes in the Solimões and Beni‐Madeira Rivers of the Amazon basin. This study developed data collected over 8 years indicating large spatial and temporal variations in dissolved Sr isotopes among the rivers of the Amazon basin. The large 87Sr/86Sr variations were found to be correlated with the geology of the source areas of the suspended sediments. The Beni‐Madeira River displays a high average 87Sr/86Sr ratio and large 87Sr/86Sr fluctuations during the hydrological cycle. This large average value and fluctuations were related to the presence of Precambrian rocks and Ordovician sediments in the source area of the suspended sediment of the river. In contrast, the Solimões River displays a narrow range of Sr isotope ratio variations and an average value close to 0.709. This river drains mostly Phanerozoic rocks of northern Peru and Ecuador that are characterized by low Sr isotope ratios. The isotopic fluctuations in the Beni‐Madeira River were observed to propagate downstream at least as far as Óbidos. This signal is characterized by an inverse relationship between the concentration of elemental Sr and its isotopic ratios. We further demonstrate that the Sr isotopic composition and content in the Beni‐Madeira River is controlled by suspended sediments derived from the Andes. Despite draining areas underlain by Precambrian rocks and having high 87Sr/86Sr ratios, such rivers as the Negro and Tapajós play a minor role in the total Sr budget of the Amazon basin. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

19.
Strontium isotopic analyses of additional samples of the McCartys basalt flow (Holocene) exhibit no evident correlation with distance from the source crater or with strontium content. This confirms our previous comments urging caution in sampling of one basalt flow in order to determine its “source” initial87Sr/86Sr.  相似文献   

20.
The hypothesis that seawater was the source of the hydrothermal fluid which formed the Upper Cretaceous ophiolitic cupriferous pyrite ore desposits of the Troodos Massif (Cyprus) has been tested by analysing the strontium isotopic composition of thirteen mineralized samples from four mines. Initial87Sr/86Sr ratios range from 0.7052 ± 0.0001 to 0.7075 ± 0.0002, the latter value being indistinguishable from that of Upper Cretaceous seawater at 0.7076 ± 0.0006 (2σ). Hence, the mineralized metabasalt samples have been contaminated with87Sr, relative to initial magmatic strontium isotope ratios of the Troodos ophiolitic complex (0.70338 ± 0.00010 to 0.70365 ± 0.00005).Since seawater was the only source of strontium available during formation of the Troodos Complex which was isotopically relatively enriched in87Sr, the data confirm that seawater was the source of the hydrothermal oreforming fluid.  相似文献   

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