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1.
Chemical and isotopic data for 23 geothermal water samples collected in New Zealand within the Taupo Volcanic Zone (TVZ) are reported. Major and trace elements including Li, B and Sr and their isotopic compositions (δ7Li, δ11B, 87Sr/86Sr) were determined in high temperature geothermal waters collected from deep boreholes in different geothermal fields (Ohaaki, Wairakei, Mokai, Kawerau and Rotokawa geothermal systems). Lithium concentrations are high (from 4.5 to 19.9 mg/L) and Li isotopic compositions (δ7Li) are homogeneous, ranging between −0.5‰ and +1.4‰. In particular, it is noteworthy that, except for the samples from the Kawerau geothermal field having slightly higher δ7Li values (+1.4%), the other geothermal waters have a near constant δ7Li signature around a mean value of 0‰ ± 0.6 (2σ, n = 21). Boron concentrations are also high and relatively homogeneous for the geothermal samples, falling between 17.5 and 82.1 mg/L. Boron isotopic compositions (δ11B) are all negative, and display a range between −6.7‰ and −1.9‰. These B isotope compositions are in agreement with those of the Ngawha geothermal field in New Zealand. Lithium and B isotope signatures are in a good agreement with a fluid signature mainly derived from water/rock interaction involving magmatic rocks with no evidence of seawater input. On the other hand, Sr concentrations are lower and more heterogeneous and fall between 2 and 165 μg/L. The 87Sr/86Sr ratios range from 0.70549 to 0.70961. These Sr isotope compositions overlap those of the Rotorua geothermal field in New Zealand, confirming that some geothermal waters (with more radiogenic Sr) have interacted with bedrocks from the metasedimentary basement. Each of these isotope systems on their own reveals important information about particular aspects of either water source or water/rock interaction processes, but, considered together, provide a more integrated understanding of the geothermal systems from the TVZ in New Zealand.  相似文献   

2.
The groundwater B concentration in Mesozoic karst, Neogene and alluvial aquifers in the West part of Chalkidiki province in Central Macedonia, Greece reaches 6.45 mg L−1, which exceeds the limit of 1 mg L−1, set by the European Union for drinking water. The high B contents have been detected in this area, not only near the shoreline, where seawater intrusion occurs, but also in the inland part of the basin. Multi isotope (2H, 18O, 34S, 18O(SO4), 11B, 87Sr/86Sr) data from borehole and thermal water springs allow identification of the possible B sources. The B dissolved in groundwater in the Chalkidiki area is mainly geogenic. The low δ11B values, 0–1‰, similar to those of thermal fluids from continental geothermal fields, and the low Cl/B ratio compared to seawater both indicate a geothermal origin for B and reflect deep circulation and interaction with igneous rocks. The 87Sr/86Sr ratio also indicates that the deep-aquifer granodiorite is the predominant rock source of Sr, while the shallow limestone unit has negligible effects on the dissolved Sr budget in these thermal karst waters which O and H isotopes show to be of meteoric origin. The main source of high B in borehole water is mainly mixing with B-rich geothermal water. The mixing between geothermal water and water from the Neogene aquifer is also reflected by isotopic contents of SO4.  相似文献   

3.
Analyses of environmental isotopes (18O, 2H, and 87Sr/86Sr) are applied to groundwater studies with emphasis on saline groundwater in aquifers in the Keta Basin, Ghana. The 87Sr/86Sr ratios of groundwater and surface water of the Keta Basin primarily reflect the geology and the mineralogical composition of the formations in the catchments and recharge areas. The isotopic compositions of 18O and 2H of deep groundwater have small variations and plot close to the global meteoric water line. Shallow groundwater and surface water have considerably larger variations in isotopic compositions, which reflect evaporation and preservation of seasonal fluctuations. A significant excess of chloride in shallow groundwater in comparison to the calculated evaporation loss is the result of a combination of evaporation and marine sources. Groundwaters from deep wells and dug wells in near-coastal aquifers are characterized by relatively high chloride contents, and the significance of marine influence is evidenced by well-defined mixing lines for strontium isotopes, and hydrogen and oxygen stable isotopes, with isotopic compositions of seawater as one end member. The results derived from environmental isotopes in this study demonstrate that a multi-isotope approach is a useful tool to identify the origin and sources of saline groundwater. Electronic Publication  相似文献   

4.
Isotopic and chemical composition of groundwater from wells and springs, and surface water from the basalt-dominated Axum area (northern Ethiopia) provides evidence for the origin of water and dissolved species. Shallow (depth < 40 m) and deep groundwater are distinguished by both chemical and isotopic composition. Deep groundwater is significantly enriched in dissolved inorganic carbon up to 40 mmol l−1 and in concentrations of Ca2+, Mg2+, Na+ and Si(OH)4 compared to the shallow type.The δ2H and δ18O values of all solutions clearly indicate meteoric origin. Shifts from the local meteoric water line are attributed to evaporation of surface and spring water, and to strong water–rock interaction. The δ13CDIC values of shallow groundwater between −12 and −7‰ (VPDB) display the uptake of CO2 from local soil horizons, whereas δ13CDIC of deep groundwater ranges from −5 to +1‰. Considering open system conditions with respect to gaseous CO2, δ13CDIC = +1‰ of the deep groundwater with highest PCO2 = 10−0.9 atm yields δ13CCO2(gas) ≈ −5‰, which is close to the stable carbon isotopic composition of magmatic CO2. Accordingly, stable carbon isotope ratios within the above range are referred to individual proportions of CO2 from soil and magmatic origin. The uptake of magmatic CO2 results in elevated cations and Si(OH)4 concentrations. Weathering of local basalts is documented by 87Sr/86Sr ratios of the groundwater from 0.7038 to 0.7059. Highest values indicate Sr release from the basement rocks. Besides weathering of silicates, neoformation of solids has to be considered, which results in the formation of, e.g., kaolinite and montmorillonite. In several solutions supersaturation with respect to calcite is reached by outgassing of CO2 from the solution leading to secondary calcite formation.  相似文献   

5.
The molecular hydrogen isotope composition (δD) of leaf waxes from terrestrial plants is increasingly used to infer hydrological characteristics of ancient high latitude climates. Analysis of the hydrogen isotope composition of n-alkanes (δDn-alkane) from a global dataset of individual plants growing at low and middle latitudes indicates that plant ecological life form is an important factor in determining the hydrogen isotope fractionation. However, environmental and biological controls of high latitudinal leaf wax δD values are poorly understood because of a lack of δD records from modern flora in these regions. We previously noticed smaller apparent hydrogen isotope fractionations between n-alkanes and environmental water (εalk-water) in deciduous trees growing at high latitudes (>59°N; Liu, W.-G., Yang, H., 2008. Multiple controls for the variability of hydrogen isotopic compositions in higher plant n-alkanes from modern ecosystems. Global Change Biology 14, 2166-2177.) To further examine these issues, we measured δDn-alkane from a variety of plants that inhabit high latitude environments and added critically needed leaf wax δD data from grass and herbs to the existing global δDn-alkane database. Inclusion of these new data with the existing global dataset (n = 408) confirms plant ecological life form as an important control for leaf wax δD variation for terrestrial plants living at high latitudes. Our results suggest that, while precipitation δD is captured in these high latitude plants, physiological characters such as leaf area, venation pattern and hydraulic system, that enhance transpiration rate during summer growth, may impart δDn-alkane differences among plants with different ecological life forms.  相似文献   

6.
The Yangbajing geothermal field with the highest reservoir temperature among Chinese hydrothermal systems is located about 90 km northwest to Lhasa City, capital of Tibet, where high temperature geothermal fluids occur in two reservoirs: a shallow one at a depth of 180–280 m and a deep one at 950–1,850 m. In this study, Oxygen-18 and deuterium isotope compositions as well as 87Sr/86Sr ratios of water samples collected from geothermal wells, cold springs and surface water bodies were characterized to understand the genesis of geothermal fluids at Yangbajing. The results show that the deep geothermal fluid is the mixing product of both magmatic and infiltrating snow-melt water, whereas the shallow geothermal fluid is formed by the mixing of deep geothermal fluid with cold groundwater. Using a binary mixing model with deep geothermal fluid and cold groundwater as two endmembers, the mixing ratios of the latter in most shallow geothermal water samples were calculated to be between 40 and 50%. The combined use of O, H, and Sr isotopes proves to be an effective approach to depict the major sources of geothermal fluids and the mixing processes occurring in two reservoirs at Yangbajing.  相似文献   

7.
The FEBEX experiment is a 1:1 simulation of a high level waste disposal facility in crystalline rock according to the Spanish radwaste disposal concept. This experiment has been performed in a gallery drilled in the underground laboratory Grimsel Test Site (Switzerland). Two boreholes parallel to the FEBEX drift were drilled 20 and 60 cm away from the granite–bentonite interface to provide data on potential bentonite–granite solutes transfer. Periodic sampling and analysis of the major ions showed: (a) the existence of solutes transfer from the bentonite porewater towards the granite groundwater, explaining the Cl− and Na+ contents of the latter; (b) that the concentration of the natural tracers coming into the granite groundwater from the bentonite porewater increased over time. This bentonite–granite solutes transfer was modelled in order to predict the increase in the Cl− and Na+ concentrations of the granite groundwater. The modelled results seem to confirm that the mechanism of solute migration in this scenario is that of diffusive transport. An effective diffusion coefficient of De = 5 × 10−11 m2/s was that which best fitted the data obtained.  相似文献   

8.
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9.
Karst rocks from the Huanglong Formation exposed at the margin of the Eastern Sichuan Basin can be divided into four types:slightly corroded, moderately corroded porous, intensely corroded brecciated and intensely corroded and replaced secondary calcic karstic rocks. The carbon, oxygen and strontium isotope compositions of the various karst rocks are analyzed systematically and compared to rocks without karst corrosion. The results indicate that(1) the Huanglong Formation in the eastern Sichuan Basin was a restricted bay supplied and controlled by freshwater in which mudmicrite and mud-dolomicrite exhibit low δ13C and δ18O values and high 87Sr/86 Sr ratios;(2) all types of karstic rocks in the paleokarst reservoirs of the Huanglong Formation in the research area are affected by atmospheric freshwater with the δ13C and δ18O values and 87Sr/86 Sr ratios in the original formation approaching those of atmospheric freshwater, which reflects ancient hydrological conditions, fluid properties, isotopic source and the fractionation effect;(3) the intensely corroded and replaced secondary limestone is affected by a variety of diagenetic fluids, often reflected by δ13C and δ18O values, while the 87Sr/86 Sr ratios exhibit the strong degree of the corrosion;(4) after comparing the 87Sr/86 Sr ratios of each type of karst rock, the diagenetic fluids are determined to be mainly atmospheric freshwater, and depending on the strength of corrosion, and the low 87Sr/86 Sr ratio fluids in the layer will participate in the karst process. The carbon, oxygen, and strontium isotopes of different karstic reservoirs can provide meaningful geochemical information for forecasting and evaluating the development and distribution rules of the Huanglong Formation at the margin of the eastern Sichuan Basin in time and space.  相似文献   

10.
This paper describes an indirect method to calculate the isotopic composition of rainfall by using the isotopic composition of karst springs fed by waters circulating in the most important regional aquifer of central Italy, i.e. the Mesozoic limestone sequence that forms the backbone of the Apennines. By using δ18O and δD data and the δ18O (and/or δD) average gradient for elevation, evaluated through the use of literature rainfall data and new measurements from a typical Alpine valley in northern Italy, the altitude of precipitation of their parent water has been re-calculated. Vertical descents of more than 2000 m, from recharge to discharge, have been assessed in some high flow-rate cold springs in the morphologically steep Adriatic sector of central Italy. A clear correlation between the vertical descents and more negative isotopic compositions at their relative emergence elevations is highlighted. In contrast, in the Tyrrhenian sector lower karstic drops (generally lower than 500 m) correlate with less negative isotopic composition of recharge areas.The δ18O iso-contour map of the “recalculated” parent rainfall in central Italy is more detailed than any possible isotopic map of rainfall made using pluviometers, unless large number of rainfall collectors were deployed on mountaintops. The data also show that the isotopic composition of rainfall depends on the source of the storm water. In particular, precipitation is isotopically heavier when originating in the Mediterranean Sea, and lighter when formed in the Atlantic Ocean. Consequently, the collision between air masses with such a different isotopic signature results in a relatively small latitudinal fractionation effect. The peninsular part of central Italy is very narrow, with several mountains and massifs more that 2000 m high, and any latitudinal variation in the isotopic composition between rainfall sourced in the Atlantic Ocean and in the Mediterranean Sea is much lower than that due to the isotopic fractionation due to elevation.  相似文献   

11.
In the Tivoli Plain (Rome, Central Italy) the interaction between shallow and deep groundwater flow systems enhanced by groundwater extraction has been investigated using isotopic and chemical tracers. A conceptual model of the groundwater flowpaths has been developed and verified by geochemical modeling. A combined hydrogeochemical and isotopic investigation using ion relationships such as DIC/Cl−, Ca/(Ca + Mg)/SO4/(SO4 + HCO3), and environmental isotopes (δ18O, δ2H, 87Sr/86Sr, δ34S and δ13C) was carried out in order to determine the sources of recharge of the aquifer, the origin of solutes and the mixing processes in groundwater of Tivoli Plain. Multivariate statistical methods such as principal component analysis and Cluster analyses have confirmed the existence of different geochemical facies and the role of mixing in the chemical composition of the groundwater.  相似文献   

12.
The study area is located in the border of the high and low folded zone having a semi-arid climate area. This study initiated in 2009–2010, deals essentially with the investigation of the stable isotope (18O and deuterium 2H) as well as radioactive isotope represented by tritium 3H in rain, carbonate springs, intergranular aquifer, and surface water in order to investigate the source and relative ages of the groundwater and to show the influence of the altitude variations of the isotope composition. In this study and for the first time in the area, a local meteoric water line have been drawn with an empirical formula δ 2H?=?7.7δ 18O?+?14.4. The δ 18O–altitude effect was determined using isotopic data for several samples taken from groundwater and surface water; it was approximated at ?0.79?‰/100 m for the entire area of the study. The output of the tritium concentrations in the springs and water well samples revealed to the conclusion that the values closely resembles to the present time tritium concentration in precipitation.  相似文献   

13.
Ice core from Greenland was melted, filtered, homogenised, loaded into glass ampoules, sealed, autoclaved to eliminate biological activity, and calibrated by dual‐inlet isotope‐ratio mass spectrometry. This isotopic reference material (RM), USGS46, is intended as one of two secondary isotopic reference waters for daily normalisation of stable hydrogen (δ2H) and stable oxygen (δ18O) isotopic analysis of water with a mass spectrometer or a laser absorption spectrometer. The measured δ2H and δ18O values of this reference water were ?235.8 ± 0.7‰ and ?29.80 ± 0.03‰, respectively, relative to VSMOW on scales normalised such that the δ2H and δ18O values of SLAP reference water are, respectively, ?428 and ?55.5‰. Each uncertainty is an estimated expanded uncertainty (U = 2uc) about the reference value that provides an interval that has about a 95‐percent probability of encompassing the true value. This reference water is available in cases containing 144 glass ampoules that are filled with either 4 ml or 5 ml of water per ampoule.  相似文献   

14.
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15.
The West Coast belt, consisting of nearly 60 thermal springs, is one of the most diversified geothermal fields in India. The present work describes the multi-isotopic (O, H, C, S, B and Sr) characterization of thermal waters carried out in the Tural-Rajwadi geothermal field, situated in southern sector of the west coast geothermal area. The aim of this study is to delineate the origin of thermal water as well as to ascertain the sources of carbon, sulphur, boron and strontium dissolved in those thermal springs. The stable isotopes (δ2H and δ18O) and tritium data indicate that these thermal springs are not recently recharged rain water rather, it contains very old component of water. Oxygen-18 shift is observed due to rock-water interaction over a long period of time. Carbon isotopic composition of DIC points out to the silicate weathering with soil CO2 coming from C3 type of plants whereas δ34S of dissolved sulphate confirms the marine origin of sulphate. This marine signature is basically derived from paleo-seawater possibly entrapped within the flows. Boron isotopic data reveals that both the seawater and rock dissolution are the sources of boron in the thermal waters whereas high 87Sr/86Sr ratios (0.7220–0.7512) of the thermal waters conclusively establishes that archean granitic basement is the predominant rock source of strontium, not the Deccan flood basalts. In addition, like strontium, concentrations of lithium, rubidium and caesium are also governed by the rock-water interaction. Thus, the combined use of this multi-isotope technique coupled with trace element concentrations proves to be an effective tool to establish the sources of solutes in the thermal water.  相似文献   

16.
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17.
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   

18.
《Applied Geochemistry》1997,12(3):305-319
An analysis of the S and O isotopic compositions and concentrations of dissolved S04 in river-and lake-water from 7 major catchments of the North and South Islands, New Zealand, allows the distinction between natural (geological, geothermal and volcanic) and anthropogenic S sources.The Buller and the Wairau, relatively pristine rivers in the South Island, show two end-member mixing between34S- and18O-rich rain-water S04 (relatively enriched isotope values) and relatively depleted S04 from oxidation of bedrock sulfide. Tertiary sediments contribute the isotopically most depleted S (down to δ34SCDT−15‰) to the river-water S04, whereas Mesozoic greywacke contributes S with slightly positive δ34S values. River-water S04δ18OSMOW values range from 0 to + 5‰ most probably depending on the micro-environment of the oxidising zone. South Island rivers with S04δ34S> + 5‰ have low S04 concentrations (< 3 mgl−1) and are dominantly composed of rain-water S04 which is principally sea-water derived. In the North Island, the Hutt River S04 samples also lie on an isotopic mixing trend from “greywacke bedrock” to rain-water S04, the latter with δ34S and δ18O values up to + 16 and + 6‰ respectively and a So4/SO4 + Cl fraction of 0.15 (sea-water is 0.12. Although dominated by greywacke, some samples in the Wairarapa area have relatively enriched δ18Sand δ34S values and elevated S04 concentrations (up to 16 mgl−), together with higher SO4/SO4 + Cl fraction ratios. This suggests input of fertilizer S04 (δ34S+ 17.2‰andδ18O+ 12.7‰) in the rivers of this agricultural area. The fertilizer loading of the Ruamahanga river can be estimated by its graphical offset from a deduced baseline for bedrockrainfall derived S04 on a S versus O isotope plot. The fertilizer loading represents about 20% of the S04 in the river. Extrapolation of this figure to the annual river discharge indicates that approximately 18% of the amount applied within the catchment is lost to the river.The source of the Whangaehu river is the Ruapehu crater lake (active volcano) with high S04 concentrations and very enriched S04 isotopic signatures (δ34S> + 17‰andδ18O> + 12‰). Downstream this water is diluted by tributaries with lower S04 concentration and isotope signatures of Tertiary sediments similar to the rivers in the South Island. Both geothermal and rain-water S04 inputs to the streams flowing into Lakes Taupo and Rotorua were identified isotopically; in particular waters flowing out from Lake Rotorua have a higher geothermal derived S04 content than the inflows, indicating that there must be a considerable underwater geothermal input to the lake.  相似文献   

19.
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20.
The stable isotopic characteristics were used together with the total chloride to assess changes in groundwater from recharge zones into the carbonate aquifer in an arid environment. The aquifer under study represents a major source of groundwater and thermal springs in Al-Ain city, which are located at the northern part of Jabal Hafit in the United Arab Emirates (UAE). The relationship between oxygen and hydrogen isotopic composition of groundwater is established and is described by δD?=?2.2δ18O???9.96. The lower slope and y-intercept of groundwater samples relative to the local meteoric waterline suggests that the isotopic enrichment is due to the evaporation of shallow groundwater after recharge occurs. The majority of the shallow groundwater samples have a negative deuterium excess (d-excess) which might be ascribed to high a degree of evaporation, while most of the groundwater samples from deep wells, have a positive value of d-excess which may be related to a low degree of evaporation. The δ18O values of the thermal waters suggest enrichment towards δ18O of the carbonate rocks because of the exchange with oxygen at higher temperatures. A possible mixing between thermal or hot water and shallow groundwater is evident in some samples as reflected by δD vs. Cl and d-excess vs. δ18O plots.  相似文献   

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