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1.
A seawater-intrusion study was conducted at an oil-refinery site located on the coast in the lower Esino Valley, Italy. A steady-state density-dependent flow model was used in order to understand the position of the freshwater/salt-water interface, as influenced by the hydrogeologic structure and the presence of industrial activities and a river. Collected data and model results showed that in a large part of the area, the salt-water interface is steep and can penetrate only a few meters inland. On the other hand, close to the river mouth, seawater represents the main saline source for the aquifer. The river, in connection with the sea, can enhance seawater encroachment into the coastal aquifer; a long-term survey of river level and chloride concentrations in groundwater is recommended to further improve the physical model and to obtain a better calibration. At the refinery site, two “secondary” sources of saline water were identified and were demonstrated to have had a great influence on the presence of brackish waters in the unconfined aquifer: leakage from the fire-extinguishing system (network of pipes containing seawater) and rough sea events. This confirmed that groundwater contamination by chloride can result from means other than seawater intrusion.  相似文献   

2.
A series of karstic springs in Israel belongs either to the western (Mediterranean) or eastern (Rift Valley) watersheds. Most of them are presently managed or diverted. Salinities range from very fresh through brackish to very saline waters.  相似文献   

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

4.
This study is an attempt to quantify the geochemical processes and the timescale of seawater intrusion into a coastal aquifer from changes in the major ionic composition of the water and the natural distribution of the cosmogenic isotopes 14C and 3H. For that purpose, we sampled saline and brackish groundwaters from the Israeli coastal aquifer. A multilayer sampler (MLS) was used to obtain very high resolution (10 cm) profiles across the fresh-saline water interface (FSI).The chemical and stable isotope data revealed three distinct water types (end members) that are located in different zones on the route to the coastal aquifer: (1) slightly modified Mediterranean seawater (SWS); (2) slightly diluted (with up to 20% fresh groundwater) saline groundwater (SDS); and (3) fresh groundwater (FGW).The SWS samples generally show an excess of total alkalinity and total dissolved inorganic carbon (DIC), and a depletion of 13CDIC and 14CDIC with respect to normal seawater indicating that anaerobic oxidation of organic matter is the first diagenetic reaction that affects seawater during its penetration into the bottom sediments. SDS waters appear when SWS is slightly diluted, gain Ca2+ and Sr2+, and is depleted in K+, suggesting that the main processes that transform SWS into SDS are slight dilution with fresh groundwater and cation exchange. At the fresh-saline water interface, SDS generally shows conservative mixing with FGW.Inspection of chemical data from coastal aquifers around the world indicates that intensive ion exchange in slightly diluted saline groundwater is a globally important phenomenon of seawater intrusion. Most of our saline groundwater samples contain substantial amounts of 3H suggesting that penetration of Mediterranean seawater and its inland travel to a distance of 50-100 m onshore occurred 15-30 yr ago. This is supported by the 14CDIC mass balance that explains the relatively low 14CDIC activities in the SDS as influenced by diagenesis and not by simple radioactive decay.  相似文献   

5.
《Applied Geochemistry》1988,3(2):185-203
Chemical and isotopic analyses of water from drill holes and mines throughout the Fennoscandian Shield show that distinct layers of groundwater are present. An upper layer of fresh groundwater is underlain by several sharply differentiated saline layers, which may differ in salinity, relative abundance of solutes, and O, H, Sr and S isotope signature. Saline groundwater can be classified into four major groups based on geochemistry and presumed origin. Brackish and saline waters from 50–200 m depth in coastal areas around the Baltic Sea exhibit distinct marine chemical and isotopic fingerprints, modified by reactions with host rocks. These waters represent relict Holocene seawater. Inland, three types of saline groundwater are observed: an uppermost layer of brackish and saline water from 300–900 m depth; saline water and brines from 1000–2000 m depth; and superdeep brines which have been observed to a depth of at least 11 km in the drill hole on the Kola Peninsula, U.S.S.R. Electrical and seismic studies in shield areas suggest that such brines are commonly present at even greater depths. The salinity of all inland groundwaters is attributed predominantly to water-rock interaction. The main solutes are Cl, Ca, Na and Mg in varying proportions, depending on the host rock lithology. The abundance of dissolved gases increases with depth but varies from site to site. The main gas components are N2, CH4 (up to 87 vol.%) and locally H2. The δ13C value for methane is highly variable (−25 to −46%), and it is suggested that hydrothermal or metamorphic gases trapped within the surrounding rocks are the most obvious source of CH4. The uppermost saline water has meteoric oxygen-hydrogen isotopic compositions, whereas values from deeper water plot above the meteoric water line, indicating considerably longer mean residence time and effective low temperature equilibration with host rocks. Geochemical and isotopic results from some localities demonstrate that the upper saline water cannot have been formed through simple mixing between fresh water and deep brines but rather is of independent origin. The source of water itself has not been satisfactorily verified although superdeep brines at least may contain a significant proportion of relict Precambrian hydrothermal or metamorphic fluids.  相似文献   

6.
唐山曹妃甸浅层水咸化机制及反向模拟   总被引：2，自引：0，他引：2  
王聪  梁杏  李静 《地质科技情报》2012,31(3):104-108,115
采集了唐海至渤海湾剖面的13组水样,分析了研究区浅层地下水的化学特征及成因机制.运用Phreeqc软件反向模拟了地下水流路径上浅层微咸水(咸水)的补给机理及咸化过程.结果显示:浅层地下水由北向南,ρ(TDS)由0.36 g/L逐渐上升到39.2 g/L,水化学类型从HCO3·Cl-Ca·Mg·Na型过渡为Cl· HCO3-Na型再转变为Cl-Na· Mg型.微咸水形成以咸淡混合为主,期间伴随着岩盐、斜长石、CO2、高岭石、钾长石、石膏的溶解及钙蒙脱石、方解石的沉淀析出.咸水形成初期主要受海水入侵影响,后期受蒸发作用影响又进一步咸化.  相似文献   

7.
Pollution of groundwater by seawater intrusion poses a threat to sustainable agriculture in the coastal areas of Korea. Therefore, seawater intrusion monitoring stations were installed in eastern, western, and southern coastal areas and have been operated since 1998. In this study, groundwater chemistry data obtained from the seawater intrusion monitoring stations during the period from 2007 to 2009 were analyzed and evaluated. Groundwater was classified into fresh (<1,500 μS/cm), brackish (1,500–3,000 μS/cm), and saline (>3,000 μS/cm) according to EC levels. Among groundwater samples (n = 233), 56, 7, and 37% were classified as the fresh, brackish, and saline, respectively. The major dissolved components of the brackish and saline groundwaters were enriched compared with those of the fresh groundwater. The enrichment of Na+ and Cl− was especially noticeable due to seawater intrusion. Thus, the brackish and saline groundwaters were classified as Ca–Cl and Na–Cl types, while the fresh groundwater was classified as Na–HCO3 and Ca–HCO3 types. The groundwater included in the Na–Cl types indicated the effects of seawater mixing. Ca2+, Mg2+, Na+, K+, SO4 2−, and Br− showed good correlations with Cl− of over r = 0.624. Of these components, the strong correlations of Mg2+, SO4 2−, and Br− with Cl− (r ≥ 0.823) indicated a distinct mixing between fresh groundwater and seawater. The Ca/Cl and HCO3/Cl ratios of the groundwaters gradually decreased and approached those of seawater. The Mg/Cl, Na/Cl, K/Cl, SO4/Cl, and Br/Cl ratios of the groundwaters gradually decreased, and were similar to or lower than those of seawater, indicating that Mg2+, Na+, K+, SO4 2−, and Br−, as well as Cl− in the saline groundwater can be enriched by seawater mixing, while Ca2+ and HCO3 − are mainly released by weathering processes. The influence of seawater intrusion was evaluated using threshold values of Cl− and Br−, which were estimated as 80.5 and 0.54 mg/L, respectively. According to these criteria, 41–50% of the groundwaters were affected by seawater mixing.  相似文献   

8.
We hypothesize that nutrient cycling in a Gulf of Mexico subterranean estuary (STE) is fueled by oxygen and labile organic matter supplied by tidal pumping of seawater into the coastal aquifer. We estimate nutrient production rates using the standard estuarine model and a non-steady-state box model, separate nutrient fluxes associated with fresh and saline submarine groundwater discharge (SGD), and estimate offshore fluxes from radium isotope distributions. The results indicate a large variability in nutrient concentrations over tidal and seasonal time scales. At high tide, nutrient concentrations in shallow beach groundwater were low as a result of dilution caused by seawater recirculation. During ebb tide, the concentrations increased until they reached a maximum just before the next high tide. The dominant form of nitrogen was dissolved organic nitrogen (DON) in freshwater, nitrate in brackish waters, and ammonium in saline waters. Dissolved organic carbon (DOC) production was two-fold higher in the summer than in the winter, while nitrate and DON production were one order of magnitude higher. Oxic remineralization and denitrification most likely explain these patterns. Even though fresh SGD accounted for only ∼5% of total volumetric additions, it was an important pathway of nutrients as a result of biogeochemical inputs in the mixing zone. Fresh SGD transported ∼25% of DOC and ∼50% of total dissolved nitrogen inputs into the coastal ocean, with the remainder associated with a one-dimensional vertical seawater exchange process. While SGD volumetric inputs are similar seasonally, changes in the biogeochemical conditions of this coastal plain STE led to higher summertime SGD nutrient fluxes (40% higher for DOC and 60% higher for nitrogen in the summer compared to the winter). We suggest that coastal primary production and nutrient dynamics in the STE are linked.  相似文献   

9.
Saline groundwaters were recovered from undisturbed (Restigouche deposit) and active (Brunswick #12 mine) Zn-Pb volcanogenic massive sulfide deposits in the Bathurst Mining Camp (BMC), northern New Brunswick, Canada. These groundwaters, along with fresh to brackish meteoric ground and surface waters from the BMC, have been analyzed to determine their major, trace element and stable isotopic (O, H, C, and B) compositions. Saline groundwaters (total dissolved solids = 22-45 g/L) are characterized by relatively high Na/Ca ratios compared to brines from the Canadian Shield and low Na/Clmolar and δ11B isotopic compositions (−2.5‰ to 11.1‰) compared to seawater. Although saline waters from the Canadian Shield commonly have oxygen and hydrogen isotopic compositions that plot to the left of the global meteoric water line, those from the BMC fall close to the water line. Fracture and vein carbonate minerals at the Restigouche deposit have restricted carbon isotopic compositions of around −5‰ to −6‰. The carbon isotopic compositions of the saline waters at the Restigouche deposit (+12‰ δ13CDIC) are the result of fractionation of dissolved inorganic carbon by methanogenesis. We suggest that, unlike previous models for shield brines, the composition of saline waters in the BMC is best explained by prolonged water-rock reaction, with no requirement of precursor seawater. We suggest that elevated Br/Cl ratios of saline waters compared to seawater may be explained by differential uptake of Br and Cl during groundwater evolution through water-rock reaction.  相似文献   

10.
In recent years, voices in Jordan became lauder to exploit the fresh to brackish deep groundwater overlain by fresh groundwater bodies. In this article the implications of such a policy on the existing fresh water bodies are worked out through studying the sources of salinity in the different aquifer systems and the potentials of salinity mobilization by artificial changes in the hydrodynamic regimes. It is concluded that extracting the groundwater of deep aquifers overlain by fresh water bodies, whether the deep groundwater is fresh to brackish, brackish or salty, is equivalent to extracting groundwater from the overlying fresh groundwater bodies because of the hydraulic connections of the deep and the shallow aquifers’ groundwaters. The consequences are even more complicated and severe because exploiting the deep groundwater containing brackish or salty water will lead to refilling by fresh groundwater leaking from the overlying aquifers. The leaking water becomes salinized as soon as it enters the pore spaces of the emptied deep aquifer matrix and by mixing with the deep aquifer brackish or saline groundwater. Therefore, the move to exploit the deep groundwater is misleading and damaging the aquifers and is unjust to future generation's rights in the natural wealth of Jordan or any other country with similar aquifers’ set-up. In addition, desalination produces brines with high salinity which cannot easily be discharged in the highlands of Jordan (with only very limited access to the open sea) because they will on the long term percolate down into fresh water aquifers.  相似文献   

11.
In this study a typical coastal karst aquifer, developed in lower Cretaceous limestones, on the western Mediterranean seashore (La Clape massif, southern France) was investigated. A combination of geochemical and isotopic approaches was used to investigate the origin of salinity in the aquifer. Water samples were collected between 2009 and 2011. Three groundwater groups (A, B and C) were identified based on the hydrogeological setting and on the Cl− concentrations. Average and maximum Cl− concentrations in the recharge waters were calculated (ClRef. and ClRef.Max) to be 0.51 and 2.85 mmol/L, respectively). Group A includes spring waters with Cl− concentrations that are within the same order of magnitude as the ClRef concentration. Group B includes groundwater with Cl− concentrations that range between the ClRef and ClRef.Max concentrations. Group C includes brackish groundwater with Cl− concentrations that are significantly greater than the ClRef.Max concentration. Overall, the chemistry of the La Clape groundwater evolves from dominantly Ca–HCO3 to NaCl type. On binary diagrams of the major ions vs. Cl, most of the La Clape waters plot along mixing lines. The mixing end-members include spring waters and a saline component (current seawater or fossil saline water). Based on the Br/Clmolar ratio, the hypothesis of halite dissolution from Triassic evaporites is rejected to explain the origin of salinity in the brackish groundwater.Groundwaters display 87Sr/86Sr ratios intermediate between those of the limestone aquifer matrix and current Mediterranean seawater. On a Sr mixing diagram, most of the La Clape waters plot on a mixing line. The end-members include the La Clape spring waters and saline waters, which are similar to the deep geothermal waters that were identified at the nearby Balaruc site. The 36Cl/Cl ratios of a few groundwater samples from group C are in agreement with the mixing hypothesis of local recharge water with deep saline water at secular equilibrium within a carbonate matrix. Finally, PHREEQC modelling was run based on calcite dissolution in an open system prior to mixing with the Balaruc type saline waters. Modelled data are consistent with the observed data that were obtained from the group C groundwater. Based on several tracers (i.e. concentrations and isotopic compositions of Cl and Sr), calculated ratios of deep saline water in the mixture are coherent and range from 3% to 16% and 0% to 3% for groundwater of groups C and B, respectively.With regard to the La Clape karst aquifer, the extension of a lithospheric fault in the study area may favour the rise of deep saline water. Such rises occur at the nearby geothermal Balaruc site along another lithospheric fault. At the regional scale, several coastal karst aquifers are located along the Gulf of Lion and occur in Mezosoic limestones of similar ages. The 87Sr/86Sr ratios of these aquifers tend toward values of 0.708557, which suggests a general mixing process of shallow karst waters with deep saline fossil waters. The occurrence of these fossil saline waters may be related to the introduction of seawater during and after the Flandrian transgression, when the highly karstified massifs invaded by seawater, formed islands and peninsulas along the Mediterranean coast.  相似文献   

12.
The imperial Valley, Jordan-Dead Sea Rift, and the Afar and Oattara depressions, all regions below sea level and the only regions in the world so situated, are characterized by saline and hypersaline groundwaters and lakes, phenomena that to date have been solely attributed to ancient lagoons, salt dissolution, and evaporation Current subsurface seawater intrusion is herewith suggested as an additional mechanism responsible for the salination of these regions This type of dynamic seawater flow is feasible where there is (a) a base level below sea level with a hydrological continuity between the two levels, and (b) a low groundwater divide between the base levels with a shallow seawater/freshwater interface situated above the base of the aquifer  相似文献   

13.
《Applied Geochemistry》2000,15(1):51-65
The Po Valley brines represent the base level of the Quaternary aquifer located in a thick clay-sands sedimentary sequence. Geochemistry indicates that these are marine waters, evaporated to the stage of gypsum precipitation and trapped at the bottom of the basin in the late Messinian. Most of the groundwater samples collected from different springs and wells in the plain result from a mixture of these Na–Cl brines and shallow groundwaters laterally recharged by the Alpine and Apennine chains.Natural outflows of brackish waters are associated with major tectonic features. Mud volcanoes, located in the eastern sector of the Po plain, are constantly monitored as sudden chemical changes are significant precursors of seismic activity. In the western sector, calcite-filled veins isotopically record different degrees of water-rock interaction. These are outcropping fossil conduits, where mixing between shallow groundwaters and deep seated brines has occurred. The temporal continuity of the hydrological circuits allows the reconstruction of past and present groundwater circulation patterns.This paper summarises and integrates the geochemical data produced over many years in order to obtain a regional picture of brine origins and the natural mechanisms of groundwater flow.  相似文献   

14.
The low lying Western part of the Netherlands is protected from the sea by a 5 km wide stretch of dunes rising to some 50 m of height. The fresh water pocket in the dunes overlies saline groundwater and a brackish transition zone. There was during a century an extraction of fresh groundwater for drinking water, supported by artificial infiltration. This has been stopped some 30 years ago. The consequent wetting of the valuable farm area (flower cultures) behind the dunes is stronger and more extensive than could be expected from mere replenishment of the fresh water zones in the dunes. It is shown in this paper that the lateral shear flows in the brackish and saline groundwater area have displaced (and are displacing) the interfaces vertically downward. The effect of more fresh and less saline groundwater in an arbitrary groundwater column is an (extra) rise of the groundwater head of the upper fresh water part. The described slow process will continue for decades until a new equilibrium has been established. In the mean time the inner dune farm area will have to cope with a surprisingly strong and extensive water level rise.  相似文献   

15.
Evolution of the shallow groundwater quality under saline intrusion in porous aquifer system has been studied with environmental isotopes and geochemistry in the Laizhou Bay area, China. Two campaigns of water sampling from various sources were carried out in spring and winter for environmental isotopic and chemical analyses. The origin of groundwater salinity from intrusion of both modern seawater and deep brine water was identified by analysing the correlations between 18O, D, T, Cl−, SO42− and electrical conductivity. The results indicate that the brine is originated from evaporating and concentrating of intruded seawater and its δD and δ18O are different from modern seawater but similar to those of mixture of seawater with fresh groundwater. It is hard to distinguish the salinity origin in this area by the δD–δ18O relationship alone. The relations between δ18O and conductivity, Cl− and SO42− have been used to identify the salinity origin due to the distinct difference in salinity between the brine and seawater, conjunctively with use of T. A threshold of T = 12 TU was adopted to identify the origin of saline groundwater.  相似文献   

16.
Integrated hydrogeochemical and geophysical methods were used to study the salinity of groundwater aquifers along the coastal area of north Kelantan. For the hydrogeochemical investigation, analysis of major ion contents of the groundwater was conducted, and other chemical parameters such as pH and total dissolved solids were also determined. For the geophysical study, both geoelectrical resistivity soundings and reflection seismic surveys were conducted to determine the characteristics of the subsurface and groundwater contained within the aquifers. The pH values range from 6.2 to 6.8, indicating that the groundwater in the study area is slightly acidic. Low content of chloride suggests that the groundwater in the first aquifer is fresh, with an average concentration of about 15.8 mg/l and high geoelectrical resistivity (>45 ohm m). On the other hand, the groundwater in the second aquifer is brackish, with chloride concentration ranging from 500 mg/l to 3,600 mg/l and very low geoelectrical resistivity (<45 ohm m) as well as high concentration of total dissolved solids (>1,000 mg/l). The groundwater in the third aquifer is fresh, with chloride concentrations generally ranging from 2 mg/l to 210 mg/l and geoelectrical resistivity of greater than 45 ohm m. Fresh and saltwater interface in the first aquifer is generally located directly in the area of the coast, but, for the second aquifer, both hydrogeochemical and geoelectrical resistivity results indicate that the fresh water and saltwater interface is located as far as 6 km from the beach. The considerable chloride ion content initially suggests that the salinity of the groundwater in the second aquifer is probably caused by the intrusion of seawater. However, continuous monitoring of the chloride content of the second aquifer indicated no significant changes with time, from which it can be inferred that the salinity of the groundwater is not affected by seasonal seawater intrusion. Schoeller diagrams illustrate that sulphate concentrations of the groundwater of the second aquifer are relatively low compared to those of the recent seawater. Therefore, this result suggests that the brackish water in the second aquifer is probably from ancient seawater that was trapped within the sediments for a long period of time, rather than due to direct seawater intrusion.  相似文献   

17.
The study area is a small coastal plain in north-eastern Tunisia. It is drained by an ephemeral stream network and is subject to several pollutant discharges such as oilfield brine coming from a neighboring oil company and wastewater from Somâa city, located in the upstream of the plain. Furthermore, a hydraulic head near the coastal part of the aquifer is below sea level, suggesting that seawater intrusion may occur. A time-domain electromagnetic (TDEM) survey, based on 28 soundings, was conducted in Wadi Al Ayn and Daroufa plains to delineate the saline groundwater. Based on longitudinal and transversal resistivity two-dimensional pseudosections calibrated with boring data, the extent of saline water was identified. Geochemical tracers were combined with the resistivity dataset to differentiate the origin of groundwater salinization. In the upstream part of the plain, the infiltration of oilfield brine through the sandy bed of Wadi Al Ayn seems to have a considerable effect on groundwater salinization. However, in the coastal part of the aquifer, groundwater salinization is due to seawater intrusion and the saltwater is reaching an inland extent around 1.3 km from the shoreline. The contribution ratios of saline water bodies derived from the inverted chloride data vary for the oilfield brine from 1 to 13 % and for the seawater from 2 to 21 %.  相似文献   

18.
Detailed geochemical analysis of groundwater beneath 1223 km2 area in southern Bengal Basin along with statistical analysis on the chemical data was attempted, to develop a better understanding of the geochemical processes that control the groundwater evolution in the deltaic aquifer of the region. Groundwater is categorized into three types: ‘excellent’, ‘good’ and ‘poor’ and seven hydrochemical facies are assigned to three broad types: ‘fresh’, ‘mixed’ and ‘brackish’ waters. The ‘fresh’ water type dominated with sodium indicates active flushing of the aquifer, whereas chloride-rich ‘brackish’ groundwater represents freshening of modified connate water. The ‘mixed’ type groundwater has possibly evolved due to hydraulic mixing of ‘fresh’ and ‘brackish’ waters. Enrichment of major ions in groundwater is due to weathering of feldspathic and ferro-magnesian minerals by percolating water. The groundwater of Rajarhat New Town (RNT) and adjacent areas in the north and southeast is contaminated with arsenic. Current-pumping may induce more arsenic to flow into the aquifers of RNT and Kolkata cities. Future large-scale pumping of groundwater beneath RNT can modify the hydrological system, which may transport arsenic and low quality water from adjacent aquifers to presently unpolluted aquifer.  相似文献   

19.
The alluvial aquifer is the primary source of groundwater along the eastern Dead Sea shoreline, Jordan. Over the last 20 years, salinity has risen in some existing wells and several new wells have encountered brackish water in areas thought to contain fresh water. A good linear correlation exists between the water resistivity and the chloride concentration of groundwater and shows that the salinity is the most important factor controlling resistivity. Two-dimensional electrical tomography (ET) integrated with geoelectrical soundings were employed to delineate different water-bearing formations and the configuration of the interface between them. The present hydrological system and the related brines and interfaces are controlled by the Dead Sea base level, presently at 410 m b.s.l. Resistivity measurements show a dominant trend of decreasing resistivity (thus increasing salinity) with depth and westward towards the Dead Sea. Accordingly, three zones with different resistivity values were detected, corresponding to three different water-bearing formations: (1) strata saturated with fresh to slightly brackish groundwater; (2) a transition zone of brine mixed with fresh to brackish groundwater; (3) a water-bearing formation containing Dead Sea brine. In addition, a low resistivity unit containing brine was detected above the 1955 Dead Sea base level, which was interpreted as having remained unflushed by infiltrating rain.  相似文献   

20.
The sandy beachface at Cape Henlopen, Delaware, receives dissolved nutrient inputs from fresh upland groundwater and estuarine seawater and exports nutrients through intertidal and submarine groundwater discharge. The discharge of brackish beachface waters indicates that there must be additional diagenetic nutrient sources and sinks within the porous beachface aquifer. At some times of the year, diagenetic processes within the beachface remove nitrate from waters draining the beachface consistent with the stoichiometry of either denitrification or dissimilatory nitrate reduction to ammonium. Up to 50–100% of the nitrate load from the upland groundwaters is apparently reduced to N2O/N2 gas or ammonium during these periods. At other times, ammonium and nitrate are added to beachface waters consistent with the stoichiometry of organic matter remineralization and nitrification. Dissolved reactive phosphorus and silica are similarly consumed and produced by beachface processes at different times of the year, presumably by adsorption or desorption. Infiltration of reactive estuarine particles may be an additional source of nutrients and carbon that supports the diagenetic activity in the beachface aquifer. These observations suggest that sandy beachfaces are biogeochemically reactive systems that can serve as sources, sinks, and temporary reservoirs of nutrients to support the primary and secondary production of the adjacent intertidal zone.  相似文献   

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