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1.
The Wadi Watir delta in the Wadi Watir watershed is a tourist area in the arid southeastern part of the Sinai Peninsula, Egypt, where development and growth of the community on the delta are constrained by the amount of groundwater that can be withdrawn sustainably. To effectively manage groundwater resources in the Wadi Watir delta, the origin of groundwater recharge, groundwater age, and changes in groundwater chemistry in the watershed needs to be understood. Mineral identification, rock chemistry, water chemistry, and the isotopes of hydrogen, oxygen, and carbon in groundwater were used to identify the sources, mixing, and ages of groundwater in the watershed and the chemical evolution of groundwater as it flows from the upland areas in the watershed to the developed areas at the Wadi Watir delta. Groundwater in the Wadi Watir watershed is primarily from recent recharge while groundwater salinity is controlled by mixing of chemically different waters and dissolution of minerals and salts in the aquifers. The El Shiekh Attia and Wadi El Ain areas in the upper Wadi Watir watershed have different recharge sources, either from recharge from other areas or from different storm events. The downgradient Main Channel area receives groundwater flow primarily from the El Shiekh Attia area. Groundwater in the Main Channel area is the primary source of groundwater supplying the aquifers of the Wadi Watir delta.  相似文献   

2.
In the arid sub-Saharan of southern Morocco, groundwater salinization poses a direct threat for agricultural production in six oases’ basins that are irrigated by water imported from the High Atlas Mountains. Here the geospatial distribution of salinity is evaluated in shallow groundwater, springs and surface waters in the Drâa Basin, integrating major and trace element geochemistry and isotopic tracers (O, H, Sr and B). The data show that water discharge from the High Atlas Mountains to the Upper section of the Drâa Basin is characterized by both low and high salinity, a distinctive low δ18O and δ2H composition (as low as −9‰ and −66‰, respectively), typical for meteoric water from high elevation, a 87Sr/86Sr range of 0.7078–0.7094, and δ11B of 12–17‰. The Ca–Mg–HCO3, Na–Cl–SO4, and Ca–SO4 compositions as well as the Br/Cl, 87Sr/86Sr, and δ11B values of the saline water suggest dissolution of Lower Jurassic carbonates and evaporite rocks in the High Atlas Mountain catchment. Storage and evaporation of the imported water in a man-made open reservoir causes an enrichment of the stable isotope ratios with a δ18O/δ2H slope of <8 but no change in the Sr and B isotope fingerprints. Downstream from the reservoir, large salinity variations were documented in the shallow groundwater from the six Drâa oases, with systematically higher salinity in the three southern oases, up to 12,000 mg/L. The increase of the salinity is systematically associated with a decrease of the Br/Cl ratio, indicating that the main mechanism of groundwater salinization in the shallow aquifers in the Drâa oases is via salt dissolution (gypsum, halite) in the unsaturated zone. Investigation of shallow groundwater that flows to the northern Drâa oases revealed lower salinity (TDS of 500–4225) water that is characterized by depleted 18O and 2H (as low as −9‰ and −66‰, respectively) and higher 87Sr/86Sr ratios (∼0.7107–0.7115) relative to irrigation water and groundwater flow from the Upper Drâa Basin. This newly-discovered low-saline groundwater with a different isotopic imprint flows from the northeastern Anti-Atlas Jabel Saghro Mountains to the northern oases of the Lower Drâa Basin. This adjacent subsurface flow results in a wide range of Sr isotope ratios in the shallow oases groundwater (0.7084–0.7131) and appears to mitigate salinization in the three northern Drâa oases. In contrast, in the southern oases, the higher salinity suggests that this mitigation is not as affective and increasing salinization through cycles of water irrigation and salt dissolution appears inevitable.  相似文献   

3.
The Wadi Watir delta, in the arid Sinai Peninsula, Egypt, contains an alluvial aquifer underlain by impermeable Precambrian basement rock. The scarcity of rainfall during the last decade, combined with high pumping rates, resulted in degradation of water quality in the main supply wells along the mountain front, which has resulted in reduced groundwater pumping. Additionally, seawater intrusion along the coast has increased salinity in some wells. A three-dimensional (3D) groundwater flow model (MODFLOW) was calibrated using groundwater-level changes and pumping rates from 1982 to 2009; the groundwater recharge rate was estimated to be 1.58?×?106 m3/year. A variable-density flow model (SEAWAT) was used to evaluate seawater intrusion for different pumping rates and well-field locations. Water chemistry and stable isotope data were used to calculate seawater mixing with groundwater along the coast. Geochemical modeling (NETPATH) determined the sources and mixing of different groundwaters from the mountainous recharge areas and within the delta aquifers; results showed that the groundwater salinity is controlled by dissolution of minerals and salts in the aquifers along flow paths and mixing of chemically different waters, including upwelling of saline groundwater and seawater intrusion. Future groundwater pumping must be closely monitored to limit these effects.  相似文献   

4.
Stable chlorine isotopes are useful geochemical tracers in processes involving the formation and evolution of evaporitic halite. Halite and dissolved chloride in groundwater that has interacted with halite in arid non-marine basins has a δ37Cl range of 0 ± 3‰, far greater than the range for marine evaporites. Basins characterized by high positive (+1 to +3‰), near-0‰, and negative (−0.3 to −2.6‰) are documented. Halite in weathered crusts of sedimentary rocks has δ37Cl values as high as +5.6‰. Salt-excluding halophyte plants excrete salt with a δ37Cl range of −2.1 to −0.8‰. Differentiated rock chloride sources exist, e.g. in granitoid micas, but cannot provide sufficient chloride to account for the observed data. Single-pass application of known fractionating mechanisms, equilibrium salt-crystal interaction and disequilibrium diffusive transport, cannot account for the large ranges of δ37Cl. Cumulative fractionation as a result of multiple wetting-drying cycles in vadose playas that produce halite crusts can produce observed positive δ37Cl values in hundreds to thousands of cycles. Diffusive isotope fractionation as a result of multiple wetting-drying cycles operating at a spatial scale of 1–10 cm can produce high δ37Cl values in residual halite. Chloride in rainwater is subject to complex fractionation, but develops negative δ37Cl values in certain situations; such may explain halite deposits with bulk negative δ37Cl values. Future field studies will benefit from a better understanding of hydrology and rainwater chemistry, and systematic collection of data for both Cl and Br.  相似文献   

5.
Understanding groundwater salinity sources in the Gulf Coast Aquifer System (GCAS) is a critical issue due to depletion of fresh groundwater and concerns for potential seawater intrusion. The study objective was to assess sources of groundwater salinity in the GCAS using ～1,400 chemical analyses and ～90 isotopic analyses along nine well transects in the Texas Gulf Coast, USA. Salinity increases from northeast (median total dissolved solids (TDS) 340 mg/L) to southwest (median TDS 1,160 mg/L), which inversely correlates with the precipitation distribution pattern (1,370– 600 mm/yr, respectively). Molar Cl/Br ratios (median 540–600), depleted δ2H and δ18O (?24.7‰, ?4.5‰) relative to seawater (Cl/Br ～655 and δ2H, δ18O 0‰, 0‰, respectively), and elevated 36Cl/Cl ratios (～100), suggest precipitation enriched with marine aerosols as the dominant salinity source. Mass balance estimates suggest that marine aerosols could adequately explain salt loading over the large expanse of the GCAS. Evapotranspiration enrichment to the southwest is supported by elevated chloride concentrations in soil profiles and higher δ18O. Secondary salinity sources include dissolution of salt domes or upwelling brines from geopressured zones along growth faults, mainly near the coast in the northeast. The regional extent and large quantities of brackish water have the potential to support moderate-sized desalination plants in this location. These results have important implications for groundwater management, suggesting a current lack of regional seawater intrusion and a suitable source of relatively low TDS water for desalination.  相似文献   

6.
Multiple age tracers were measured to estimate groundwater residence times in the regional aquifer system underlying southwestern Oman. This area, known as the Najd, is one of the most arid areas in the world and is planned to be the main agricultural center of the Sultanate of Oman in the near future. The three isotopic age tracers 4He, 14C and 36Cl were measured in waters collected from wells along a line that extended roughly from the Dhofar Mountains near the Arabian Sea northward 400 km into the Empty Quarter of the Arabian Peninsula. The wells sampled were mostly open to the Umm Er Radhuma confined aquifer, although, some were completed in the mostly unconfined Rus aquifer. The combined results from the three tracers indicate the age of the confined groundwater is < 40 ka in the recharge area in the Dhofar Mountains, > 100 ka in the central section north of the mountains, and up to and > one Ma in the Empty Quarter. The 14C data were used to help calibrate the 4He and 36Cl data. Mixing models suggest that long open boreholes north of the mountains compromise 14C-only interpretations there, in contrast to 4He and 36Cl calculations that are less sensitive to borehole mixing. Thus, only the latter two tracers from these more distant wells were considered reliable. In addition to the age tracers, δ2H and δ18O data suggest that seasonal monsoon and infrequent tropical cyclones are both substantial contributors to the recharge. The study highlights the advantages of using multiple chemical and isotopic data when estimating groundwater travel times and recharge rates, and differentiating recharge mechanisms.  相似文献   

7.
Groundwater recharge and evolution in the Quaternary aquifer beneath the Dunhuang Basin was investigated using chemical indicators, stable isotopes, and radiocarbon data to provide guidance for regional water management. The quality of groundwater and surface water is generally good with low salinity and it is unpolluted. The dissolution of halite and sylvite from fine-grained sediments controls concentrations of Na+ and K+ in the groundwater, but Na+/Cl− molar ratios >1 in all samples are also indicative of weathering of feldspar contributing to excess Na+. The dissolution of carbonate minerals yields Ca2+ to the groundwater, thereby exerting a strong influence on groundwater salinity. The δ18O and δ2H values in unconfined groundwater are enriched along the groundwater flow path from SW to NE. In contrast, confined groundwater was depleted in heavy isotopes, with mean values of −10.4‰ δ18O and −74.4‰ δ2H. Compared with the precipitation values, all of the groundwater samples were strongly depleted in heavy isotopes, indicating that modern direct recharge to the groundwater aquifers in the plains area is quite limited. The unconfined water is generally young with radiocarbon values of 64.9–79.6 pmc. In the northern basin, radiocarbon content in the confined groundwater is less than 15 pmc and an uncorrected age of ∼15 ka, indicates that this groundwater was recharged during a humid climatic phases of the late Pleistocence or early Holocene. The results have important implications for inter-basin water allocation programmes and groundwater management in the Dunhuang Basin.  相似文献   

8.
Exploration of unconventional natural gas reservoirs such as impermeable shale basins through the use of horizontal drilling and hydraulic fracturing has changed the energy landscape in the USA providing a vast new energy source. The accelerated production of natural gas has triggered a debate concerning the safety and possible environmental impacts of these operations. This study investigates one of the critical aspects of the environmental effects; the possible degradation of water quality in shallow aquifers overlying producing shale formations. The geochemistry of domestic groundwater wells was investigated in aquifers overlying the Fayetteville Shale in north-central Arkansas, where approximately 4000 wells have been drilled since 2004 to extract unconventional natural gas. Monitoring was performed on 127 drinking water wells and the geochemistry of major ions, trace metals, CH4 gas content and its C isotopes (δ13CCH4), and select isotope tracers (δ11B, 87Sr/86Sr, δ2H, δ18O, δ13CDIC) compared to the composition of flowback-water samples directly from Fayetteville Shale gas wells. Dissolved CH4 was detected in 63% of the drinking-water wells (32 of 51 samples), but only six wells exceeded concentrations of 0.5 mg CH4/L. The δ13CCH4 of dissolved CH4 ranged from −42.3‰ to −74.7‰, with the most negative values characteristic of a biogenic source also associated with the highest observed CH4 concentrations, with a possible minor contribution of trace amounts of thermogenic CH4. The majority of these values are distinct from the reported thermogenic composition of the Fayetteville Shale gas (δ13CCH4 = −35.4‰ to −41.9‰). Based on major element chemistry, four shallow groundwater types were identified: (1) low (<100 mg/L) total dissolved solids (TDS), (2) TDS > 100 mg/L and Ca–HCO3 dominated, (3) TDS > 100 mg/L and Na–HCO3 dominated, and (4) slightly saline groundwater with TDS > 100 mg/L and Cl > 20 mg/L with elevated Br/Cl ratios (>0.001). The Sr (87Sr/86Sr = 0.7097–0.7166), C (δ13CDIC = −21.3‰ to −4.7‰), and B (δ11B = 3.9–32.9‰) isotopes clearly reflect water–rock interactions within the aquifer rocks, while the stable O and H isotopic composition mimics the local meteoric water composition. Overall, there was a geochemical gradient from low-mineralized recharge water to more evolved Ca–HCO3, and higher-mineralized Na–HCO3 composition generated by a combination of carbonate dissolution, silicate weathering, and reverse base-exchange reactions. The chemical and isotopic compositions of the bulk shallow groundwater samples were distinct from the Na–Cl type Fayetteville flowback/produced waters (TDS ∼10,000–20,000 mg/L). Yet, the high Br/Cl variations in a small subset of saline shallow groundwater suggest that they were derived from dilution of saline water similar to the brine in the Fayetteville Shale. Nonetheless, no spatial relationship was found between CH4 and salinity occurrences in shallow drinking water wells with proximity to shale-gas drilling sites. The integration of multiple geochemical and isotopic proxies shows no direct evidence of contamination in shallow drinking-water aquifers associated with natural gas extraction from the Fayetteville Shale.  相似文献   

9.
Concentration and isotope ratios (δ34SSO4 and δ18OSO4) of dissolved sulfate of groundwater were analyzed in a very large anaerobic aquifer system under the Lower Central Plain (LCP) (25,000 km2) in Thailand. Groundwater samples were collected in two different kinds of aquifers; type 1 with a saline water contribution and type 2 lateritic aquifers with no saline water contribution. Two different isotopic compositional trends were observed: in type 1 aquifers sulfate isotope ratios range from low values (+2.2‰ for δ34SSO4 and +8.0‰ for δ18OSO4) to high values (+49.9‰ for δ34SSO4 and +17.9‰ for δ18OSO4); in type 2 aquifers sulfate isotope ratios range from low values (−0.1‰ for δ34SSO4 and +12.2‰ for δ18OSO4) to high δ18OSO4 ratios (+18.4‰) but with low δ34SSO4 ratios (<+12.9‰). Isotopic comparison with possible source materials and theoretical geochemical models suggests that the sulfate isotope variation for type 1 aquifer groundwater can be explained by two main processes. One is the contribution of remnant seawater, which has experienced dissimilatory sulfate reduction in the marine clay, into recharge water of freshwater origin. This process accounts for the high salinity groundwater. The other process, explaining for the modest salinity groundwater, is the bacterial sulfate reduction of the mixture water between high salinity water and fresh groundwater. Isotopic variation of type 2 aquifer groundwater may also be explained by bacterial sulfate reduction, with slower reduction rate than that of the groundwater with saline water effect. The origin of groundwater sulfate with low δ34SSO4 but high δ18OSO4 is recognized as an important topic to be examined in a future investigation.  相似文献   

10.
A detail investigation was carried out to improve the current knowledge of groundwater salinisation processes in coastal aquifers using hydrochemical and isotopic parameters. Data of major ions for 40 wells located in the Salalah plain aquifer, Sultanate of Oman, were collected during pre-monsoon 2004 and analysed. The groundwater changes along the general flow path towards the coast from fresh (EC < 1500 μS/cm), brackish (EC: 1500–3000 μS/cm) and saline (EC > 3000 μS/cm). Results of inverse modeling simulations using PHREEQC show that dissolution of halite may be the main source of Cl and Na in the study area. Ionic delta calculation indicates that the depletion of Na and K and enrichment of Ca and Mg in groundwater were probably attributed to reverse ion exchange reactions. During a sampling campaign conducted in October 2015, 11 groundwater samples were collected for Cl, Br and isotopic analysis (2H/18O). Molar Cl/Br ratios in fresh groundwater were higher than those of seawater, indicating the impact of halite dissolution on the groundwater quality. For saline groundwater, these ratios were less than those of seawater, showing the influence of anthropogenic input from agriculture on the same. Relatively depleted isotopic signature of all groundwater samples show that the monsoon precipitation is the main source of groundwater recharge in the study area.  相似文献   

11.
《Applied Geochemistry》2002,17(9):1241-1257
This study aimed to develop a methodology for assessing the hydrochemical evolution of a groundwater system, using fracture-filling and fracture-lining calcite. Fracture calcite in deep (to ca. 1000 m) granitic rocks of the Tono area, central Japan, was investigated by optical and electron microscopy, and chemical and isotopic analysis. Coupled with geological evidence, these new data imply 3 main origins for the waters that precipitated calcite: (1) relatively high-temperature hydrothermal solutions, precipitating calcite distinguished by δ18OSMOW from −3 to ca. 10‰, and with δ13CPDB from ca. −18 to −7‰; (2) seawater, probably partly of Miocene age, which precipitated calcite distinguished by δ13CPDB of ca. 0‰ and δ18OSMOW > ca. 20‰; (3) fresh water, with a variable δ13CPDB composition, but which precipitated calcite distinguished by δ13CPDB that was significantly < 0‰ and as low as ca. −29‰ and δ18OSMOW > ca. 17‰. Data for 14C suggest that at least some of the fresh-water calcite formed within the last 50 ka. The present day hydrogeological regime in the Tono area is also dominated by fresh groundwater. However, the marine calcite of probable Miocene age found at depth has shown no evidence for dissolution and many different calcite crystal forms have been preserved. Studies of other groundwater systems have correlated similar crystallographic variations with variations in the salinity of coexisting groundwaters. When this correlation is applied to the Tono observations, the calcite crystal forms imply a similar range of groundwater salinity to that inferred from the isotopic data. Thus, the present study suggests that even in presently low-salinity groundwater systems, calcite morphological variations may record the changing salinity of coexisting groundwaters. It is suggested that calcite morphological data, coupled with isotopic data, could provide a powerful palaeohydrogeological tool in such circumstances.  相似文献   

12.
The Regional Deep Cretaceous Aquifer (RDCA) is the principal groundwater resource in Syria. Isotope and hydrochemical data have been used to evaluate the geographic zones in terms of renewable and non-renewable groundwater and the inter-relation between current and past recharge. The chemical and isotopic character of groundwater together with radiometric 14C data reflect the existence of three different groundwater groups: (1) renewable groundwater, in RDCA outcropping areas, in western Syria along the Coastal and Anti-Lebanon mountains. The mean δ18O value (?7.2 ‰) is similar to modern precipitation with higher 14C values (up to 60–80 pmc), implying younger groundwater (recent recharge); (2) semi-renewable groundwater, which is located in the unconfined section of the RDCA and parallel to the first zone. The mean δ18O value (?7.0 ‰) is also similar to modern precipitation with a 14C range of 15–45 pmc; (3) non-renewable groundwater found in most of the Syrian interior, where the RDCA becomes confined. A considerable depletion in δ18O (?8.0 ‰) relative to the modern rainfall and low values of 14C (<15 pmc) suggest that the large masses of deep groundwater are non-renewable and related to an older recharge period. The wide scatter of all data points around the two meteoric lines in the δ18O-δ2H diagram indicates considerable variation in recharge conditions. There is limited renewable groundwater in the mountain area, and most of the stored deep groundwater in the RDCA is non-renewable, with corrected 14C ages varying between 10 and 35 Kyr BP.  相似文献   

13.
Deep Quaternary groundwater is the main source for industrial, domestic, and agricultural water supply in the North China Plain (NCP). There is currently a regional decline of groundwater levels, deterioration of water quality and environmental geological problems induced by increasing exploitation of the NCP Quaternary aquifer system. To trace sources and transport processes of dissolved Cl− in a regional aquifer system and to reveal hydrogeological characteristics of Quaternary complexes, δ37Cl, δ18O and δD, and chemical compositions (including F−, Cl−, Br−) of the deep groundwater sampled from the northern flow system of the NCP were measured along the west–east groundwater flow paths. The measured δ37Cl values decreased from 0.39‰ to −2.22‰ (SMOC) along the groundwater flow direction, with increasing Cl− concentrations. Marine aerosol input via rainfall is the main source of Cl− in the deep groundwater near the recharge areas, and subsequent evaporation/evapotranspiration appears to be responsible for Cl− accumulation. Mixing of recharge water with water of high-Cl− and low-δ37Cl accounts for the pattern of δ37Cl and Cl− concentration observed in Aquifer-3 along the west–east transect. The water with high-Cl and low-δ37Cl is likely from pore water released from compacted clays induced by over-exploitation of deep groundwater, suggesting that clay is a dominant subsurface source of Cl− for groundwater where a regional depression cone is present in the Quaternary aquifers. The groundwater of Aquifer-4 in the Huang-Hua depression is potentially mixed with an upward flux of Cl− from the Neogene aquifer through subvertical faults. Diffusion and ion filtration are two mechanisms invoked to explain the highly negative δ37Cl data for groundwater of Aquifer-4 in the Yanshan–Haixing areas, which provides new insight into solute migration and the hydraulic relationship in the strongly exploited groundwater system. This study using the conservative solute Cl− provides additional important information for further investigations of the geochemistry of a wide range of reactive solutes in the Quaternary aquifer system, so guiding water resource management.  相似文献   

14.
In order to address the problem of realistic assessment of groundwater potential and its sustainability, it is vital to study the recharge processes and mechanism of groundwater flow in fractured hard rocks, where inhomogeneties and discontinuities have a dominant role to play. Wide variations in chloride, δ18O and 14C concentrations of the studied groundwaters observed in space and time could only reflect the heterogeneous hydrogeological setting in the fractured granites of Hyderabad (India). This paper, based on the observed isotopic and environmental chloride variations of the groundwater system, puts forth two broad types of groundwaters involving various recharge processes and flow mechanisms in the studied granitic hard rock aquifers. Relatively high 14C ages (1300 to ～6000 yr B.P.), δ18O content (?3.2 to ?1.5‰) and chloride concentration (<100 mg/l) are the signatures that identified one broad set of groundwaters resulting from recharge through weathered zone and subsequent movement through extensive sheet joints. The second set of groundwaters possessed an age range Modern to ～1000 yr B.P., chloride in the range 100 to ～350 mg/l and δ18O from ?3.2 to +1.7‰. The δ18O enrichment and chloride concentration, further helped in the segregation of the second set of groundwaters into three sub-sets characterized by different recharge processes and sources. Based on these processes and mechanisms, a conceptual hydrogeologic model has evolved suggesting that the fracture network is connected either to a distant recharge source or to a surface reservoir (evaporating water bodies) apart from overlying weathered zone, explaining various resultant groundwaters having varying 14C ages, chloride and δ18O concentrations. The surface reservoir contribution to groundwater is evaluated to be significant (40 to 70%) in one subset of groundwaters. The conceptual hydrogeologic model, thus evolved, can aid in understanding the mechanism of groundwater flow as well as migration of contaminants to deep groundwater in other fractured granitic areas.  相似文献   

15.
Recently, Ras Sudr (the delta of Wadi Sudr) area received a great amount of attention due to different development expansion activities directed towards this area. Although Quaternary aquifer is the most prospective aquifer in Ras Sudr area, it has not yet completely evaluated. The present work deals with the simulation of the Quaternary groundwater system using a three-dimensional groundwater flow model. MODFLOW code was applied for designing the model of the Ras Sudr area. This is to recognize the groundwater potential as well as exploitation plan of the most prospective aquifer in the area. The objectives were to determine the hydraulic parameters of the Quaternary aquifer, to estimate the recharge amount to the aquifer, and to determine the hydrochemistry of groundwater in the aquifer. During this work, available data has been collected and some field investigation has been carried out. Groundwater flow model has been simulated using pilot points’ method. SEAWAT has been also applied to simulate the variable-density flow and sea water intrusion from the west. It can be concluded that: (1) the direction of groundwater flow is from the east to the west, (2) the aquifer system attains a small range of log-transformed hydraulic conductivity. It ranges between 3.05 and 3.35 m/day, (3) groundwater would be exploited by about 6.4 × 106 m3/year, (4) the estimated recharge accounts for 3 × 106 m3/year, (5) an estimated subsurface flow from the east accounts for 2.7 × 106 m3/year, (6) the increase of total dissolved solids (TDS) most likely due to dilution of salts along the movement way of groundwater from recharge area to discharge area in addition to a contribution of sea water intrusion from the west. Moreover, it is worth to note that a part of TDS increase might be through up coning from underlying more saline Miocene sediments. It is recommended that: (1) any plan for increasing groundwater abstraction is unaffordable, (2) reliable estimates of groundwater abstraction should be done and (3) automatic well control system should be made.  相似文献   

16.
Solutes in saline groundwater (total dissolved solids up to 37 000 mg/L) in the Lake Cooper region in the southern margin of the Riverine Province of the Murray Basin are derived by evapotranspiration of rainfall with minor silicate, carbonate and halite dissolution. The distribution of hydraulic heads, salinity, percentage modern carbon (pmc) contents, and Cl/Br ratios imply that the groundwater system is complex with vertical flow superimposed on lateral flow away from the basin margins. Similarities in major ion composition, stable (O, H, and C) isotope, and 87Sr/86Sr ratios between groundwater from the shallower Shepparton Formation and the deeper Calivil – Renmark aquifer also imply that these aquifers are hydraulically interconnected. Groundwater in the deeper Calivil – Renmark aquifer in the Lake Cooper region has residence times of up to 25 000 years, implying that pre-land-clearing recharge rates were <1 mm/y. As in other regions of the Murray Basin, the low recharge rates account for the occurrence of high-salinity groundwater. Shallow (<20 m) groundwater yields exclusively modern 14C ages and shows a greater influence of evaporation over transpiration. Both these observations reflect the rise of the regional water-table following land clearing over the last 200 years and a subsequent increase in recharge to 10 – 20 mm/y. The rise of the regional water-table also has increased vertical and horizontal hydraulic gradients that may ultimately lead to the export of salt from the Lake Cooper embayment into the adjacent fresher groundwater resources.  相似文献   

17.
Groundwater resources in some parts of the lower section of Shire River valley, Malawi, are not useable for rural domestic water supply due to high salinity. In this study, a combined assessment of isotopic (87Sr/86Sr, δ18O and δ2H) and major ion composition was conducted in order to identify the hydro-geochemical evolution of the groundwater and thereby the causes of salinity. Three major end-members (representing fresh- and saline groundwater, and evaporated recharge) were identified based on major ion and isotopic composition. The saline groundwater is inferred to result from dissolution of evaporitic salts (halite) and the fresh groundwater shows influence of silicate weathering. Conservative mixing models show that brackish groundwater samples result from a three component mixture comprising the identified end-members. Hence their salinity is interpreted to result from mixing of fresh groundwater with evaporated recharge and saline groundwater. On the other hand, the groundwater with low TDS, found at some distance from areas of high salinity, is influenced by mixing of evaporated recharge and fresh groundwater only. Close to the Shire marshes, where there is shallow groundwater, composition of stable isotopes of water indicates that evaporation may also be an important factor.  相似文献   

18.
The southwestern Chad basin is a semi-arid region with annual rainfall that is generally less than 500 mm and over 2,000 mm of evapotranspiration. Surface water in rivers is seasonal, and therefore groundwater is the perennial source of water supply for domestic and other purposes. Stable isotope has been measured for rainwater, surface water and groundwater samples in this region. The stable isotope data have been used to understand the inter-relationships between the rainwater, surface water, shallow and deep groundwater of this region. This is being used in a qualitative sense to demonstrate present day recharge to the groundwater. Stable isotope in rainwater for the region has an average value of –4‰ δ18O and –20‰ δ2H. Surface water samples from rivers and Lake Chad fall on the evaporation line of this average value. The Upper Zone aquifer water samples show stable isotope signal with a wide range of values indicating the complex character of the aquifer Zone with three distinguishable units. The wide range of values is attributable to waters from individual unit and/or mixture of waters of different units. The Middle and Lower aquifers Zones’ waters show similar stable isotopes values, probably indicating similarity in timing and/or mechanism of recharge. These are palaeowaters probably recharged under a climate that is different from today. The Upper Zone aquifer is presently being recharged as some of its waters show stable isotope compositions similar to those of average rainfall waters of the region.  相似文献   

19.
This paper presents results of hydrochemical and isotopic analyses of groundwater (fracture water) and porewater, and physical property and water content measurements of bedrock core at the Chalk River Laboratories (CRL) site in Ontario. Density and water contents were determined and water-loss porosity values were calculated for core samples. Average and standard deviations of density and water-loss porosity of 50 core samples from four boreholes are 2.73 ± 12 g/cc and 1.32 ± 1.24 percent. Respective median values are 2.68 and 0.83 indicating a positive skewness in the distributions. Groundwater samples from four deep boreholes were analyzed for strontium (87Sr/86Sr) and uranium (234U/238U) isotope ratios. Oxygen and hydrogen isotope analyses and selected solute concentrations determined by CRL are included for comparison. Groundwater from borehole CRG-1 in a zone between approximately +60 and −240 m elevation is relatively depleted in δ18O and δ2H perhaps reflecting a slug of water recharged during colder climatic conditions. Porewater was extracted from core samples by centrifugation and analyzed for major dissolved ions and for strontium and uranium isotopes. On average, the extracted water contains 15 times larger concentration of solutes than the groundwater. 234U/238U and correlation of 87Sr/86Sr with Rb/Sr values indicate that the porewater may be substantially older than the groundwater. Results of this study show that the Precambrian gneisses at Chalk River are similar in physical properties and hydrochemical aspects to crystalline rocks being considered for the construction of nuclear waste repositories in other regions.  相似文献   

20.
《Applied Geochemistry》2004,19(8):1233-1254
Combined hydrogeological and hydrogeochemical data allow flow systems and the origins of solutes in the Honeysuckle Creek area of the southeastern Murray Basin, which is an area affected by dryland salinity, to be constrained. Recharge occurs both on the uplands that are composed of fractured Violet Town Volcanic rocks and the Riverine Plain that comprises sediments of the Shepparton and Coonambidgal Formations. Groundwater from the Violet Town Volcanics has low salinity (<20 mmol/L Cl) and major ion geochemistry that is controlled largely by dissolution of silicate minerals. Low Cl/Br ratios (as low as 281 molar) suggest that this groundwater has not dissolved halite. Groundwater that recharged through the Riverine Plain sediments has higher Cl/Br ratios (up to 1146) and Cl concentrations of <20 mmol/L, consistent with it dissolving minor halite. Higher salinity (>20 mmol/L) groundwater has intermediate Cl/Br ratios (600–1000), which indicate that the high salinities do not simply result from halite dissolution. Rather, mixing of groundwater homogenises Cl/Br ratios, and evaporation as a consequence of a shallow water table is the dominant process that increases salinity. Oxygen and H isotopes also indicate that mixing and evaporation have occurred. These results indicate that land use over the whole region, not just the uplands, needs to be considered in any salinity management plans. Additionally future development of salinity is controlled by depth to the water table on the plains and the efficiency of recharge rather than by salt stores (halite or brines) in the unsaturated zone.  相似文献   

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