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1.
Declining water levels in arid and semi-arid regions increase an aquifer’s vulnerability to natural and anthropogenic influences. A multi-isotope (δD, δ18O, 87Sr/86Sr, and δ11B) approach was used to resolve the geochemical evolution of groundwater in a declining aquifer in a semi-arid region of the southwestern USA as groundwater composition reacts to source-water mixing, cross-formational flow including saltwater intrusion, water–rock interaction, and likely agricultural recharge. Sub-aquifers or local flow systems are present in the Southern High Plains aquifer along the Western Caprock Escarpment in New Mexico, and the study site’s local flow system contains a Na–Cl, high dissolved-solids groundwater that flows from the escarpment until it mixes with a high quality regional aquifer or regional flow system. The local flow system contains water that is similar in composition to the underlying, upper Dockum Group aquifer. Saltwater found in the upper Dockum Group aquifer likely originates in the adjacent Pecos River Basin and crosses beneath or possibly through the hydrologic divide of the Western Caprock Escarpment. Strontium concentrations of 0.9–31 mg/L and a 87Sr/86Sr range of 0.70845–0.70906 were sufficient to estimate source-water fractions, mixing patterns, and contributions from chemical weathering through mass balance inverse calculations. Boron concentrations (59–1740 mg/L) and δ11B values (+6.0–+46.0‰) were used to confirm source-water mixing, further evaluate water–rock interaction, and examine the influence of possible agricultural recharge. Alteration of B concentrations and δ11B values in an area of likely agricultural recharge indicated the loss of B and decrease in δ11B values likely from plant uptake, adsorption, and weathering contributions in the soil/vadose zone prior to recharge. The effectiveness of 87Sr/86Sr and δ11B for resolving the geochemical influences in groundwater in the Southern High Plains along the Western Caprock Escarpment allowed for the reinterpretation of the isotopic composition of water that has been shown to be highly variable in the Southern High Plains. This study shows the utility of a multi-isotope approach for resolving the geochemical evolution of groundwater in an aquifer that has a complex relationship with underlying aquifers and the applicability of these isotopes as indicators of the alteration of source waters from natural or anthropogenic influences.  相似文献   

2.
River water infiltration into an unconfined porous aquifer (∼73% gravels, ∼12% sands, ∼15% silts and clays) in the Petrignano d’Assisi plain, central Italy, was traced combining isotopic techniques (222Rn) with hydrochemical and hydrogeologic techniques in order to characterize the system under study. The 222Rn gave information about the river water residence times within the aquifer and hydrochemical data, in a two-component mixing model, which allowed estimating the extent of mixing between surface waters and groundwater in wells at increasing distances from the river. The mixing measured in the well closer to the riverbank indicated a higher contribution of river water (up to 99%) during the groundwater recession phase and a moderate contribution (up to 64%) during the recharge phase. A model describing 222Rn concentrations in groundwater as the result of both parent/daughter nuclide equilibrium and mixing process (222Rn mixing/saturation model) was used to describe observed Rn concentrations and mixing index trends with the aim of evaluating water mean infiltration velocities along the transect. The stream bank infiltration velocities obtained by the model ranged from 1 m day−1 during groundwater recharge periods, when river water infiltration is lower, to 39 m day−1 during recession phases, when river water infiltration is larger.  相似文献   

3.
Ayadi  Rahma  Trabelsi  Rim  Zouari  Kamel  Saibi  Hakim  Itoi  Ryuichi  Khanfir  Hafedh 《Hydrogeology Journal》2018,26(4):983-1007

Major element concentrations and stable (δ18O and δ2H) and radiogenic (3H and 14C) isotopes in groundwater have proved useful tracers for understanding the geochemical processes that control groundwater mineralization and for identifying recharge sources in the semi-arid region of Sfax (southeastern Tunisia). Major-ion chemical data indicate that the origins of the salinity in the groundwater are the water–rock interactions, mainly the dissolution of evaporitic minerals, as well as the cation exchange with clay minerals. The δ18O and δ2H relationships suggest variations in groundwater recharge mechanisms. Strong evaporation during recharge with limited rapid water infiltration is evident in the groundwater of the intermediate aquifer. The mixing with old groundwater in some areas explains the low stable isotope values of some groundwater samples. Groundwaters from the intermediate aquifer are classified into two main water types: Ca-Na-SO4 and Ca-Na-Cl-SO4. The high nitrate concentrations suggest an anthropogenic source of nitrogen contamination caused by intensive agricultural activities in the area. The stable isotopic signatures reveal three water groups: non-evaporated waters that indicate recharge by recent infiltrated water; evaporated waters that are characterized by relatively enriched δ18O and δ2H contents; and mixed groundwater (old/recent) or ancient groundwater, characterized by their depleted isotopic composition. Tritium data support the existence of recent limited recharge; however, other low tritium values are indicative of pre-nuclear recharge and/or mixing between pre-nuclear and contemporaneous recharge. The carbon-14 activities indicate that the groundwaters were mostly recharged under different climatic conditions during the cooler periods of the late Pleistocene and Holocene.

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4.
Hydrochemical and isotopic data of waters from the Zéroud aquifer have been used to potentially provide a means for locating occurrences and to trace movements of a variety of natural and anthropogenic recharge waters in the Zéroud Basin, Central Tunisia. Geochemical data have been measured during the dam water release, from May to September 2005, with a sampling time step of 15 days. An implication of dam water has been demonstrated that is noticeable up along the main flow path to a distance of 10 km far from the injection site. Environmental isotopes 2H, 18O and 3H of water molecule were studied to investigate the effect of dam water on the hydrological system, and an isotope balance was established to compute the contribution of water storage component in groundwater. Based on isotopic mass balance, we assess that an average of 13% of total groundwater in the upper aquifer came from dam water storage. Three distinctive recharge waters in the aquifer can be determined. Water from local rainfall (pre-dam Zéroud River) that infiltrated into the boundaries of the Draa Affane Mountain was easily distinguished from the water influenced by anthropogenic recharge located in the Zéroud right rivulet. Distinguishable isotopic signatures of native wadi Zéroud recharge due to “recent lineal recharge” through the riverbed were also identified.  相似文献   

5.
Nitrogen budget of a typical subterranean river in peak cluster karst area   总被引：2，自引：0，他引：2  
Karst groundwater is one of the important water resources for people in the world. There is an estimate that by 2028 karst groundwater will supply more than 80% of people in the world. However, several areas in the world are characterized by high nitrate concentrations in karst aquifers. In China, karst groundwater is also threatened by extensive use of fertilizer and pesticides, industry waste, septic systems and poultry, hog or cattle manure. In order to understand the water quality of a subterranean river in south China, especially the dynamic variation of nitrate, nitrogen input and output were determined via auto-monitored apparatus, manual observation and samples from 2004 to 2008 in Guancun subterranean river drainage area. Land use and anthropogenic activities were also investigated frequently. The results showed the range of nitrate variation was 2.56–15.40 mg l−1, with an average value of 6.60 mg l−1. Spatial variation of nitrate concentrations showed nitrate rose where there were villages and agriculture distribution. Long series of nitrate and discharge monitoring revealed there was a nitrate peak in spring just before the beginning of rainy season. Three rainfall events were selected for analysis of relations among hydrological process, water chemistry, and nitrate of the spring. The flood processes of the spring were divided into three or four phases according to change of water level and water chemistry. They were dominated by initial condition of aquifer, piston flow in soil and vadose, piston flow in conduit, diffuse recharge, and bypass recharge. The original condition of aquifer and rainfall pulse controlled recharge flow and changes of nitrate and hydro-chemical graphs of the spring. The quantity of nitrogen input in a year was 66.61 t, and the output was 21.24 t. Nitrogen leaching loss in base flow accounted for 76.11% in a year. Some measures should be taken to protect karst water in the very near future, so that health risks to the local people can be decreased.  相似文献   

6.
The particular objective of the present work is the development of a new radiocarbon correction approach accounting for palaeoclimate conditions at recharge and hydrochemical evolution. Relevant climate conditions at recharge are atmospheric pCO2 and infiltration temperatures, influencing C isotope concentrations in recharge waters. The new method is applied to the Ledo-Paniselian Aquifer in Belgium. This is a typical freshening aquifer where recharge takes place through the semi-confining cover of the Bartonian Clay. Besides cation exchange which is the major influencing process for the evolution of groundwater chemistry (particularly in the Bartonian Clay), also mixing with the original porewater solution (fossil seawater) occurs in the aquifer. Recharge temperatures were based on noble gas measurements. Potential infiltration water compositions, for a range of possible pCO2, temperature and calcite dissolution system conditions, were calculated by means of PHREEQC. Then the sampled groundwaters were modelled starting from these infiltration waters, using the computer code NETPATH and considering a wide range of geochemical processes. Fitting models were selected on the basis of correspondence of calculated δ13C with measured δ13C. The 14C modelling resulted in residence times ranging from Holocene to Pleistocene (few hundred years to over 40 ka) and yielded consistent results within the uncertainty estimation. Comparison was made with the δ13C and Fontes and Garnier correction models, that do not take climate conditions at recharge into account. To date these are considered as the most representative process-oriented existing models, yet differences in calculated residence times of mostly several thousands of years (up to 19 ka) are revealed with the newly calculated ages being mostly (though not always) younger. Not accounting for climate conditions at recharge (pCO2 and temperature) is thus producing substantial error on deduced residence times. The derived 14C model ages are correlated with He concentrations measured in the groundwater of the aquifer. The obtained residence times show a gap between about 14 and 21 ka indicating possible permafrost conditions which inhibited any groundwater recharge.  相似文献   

7.
The hydraulic behaviour of the karst aquifer in the Hubelj spring catchment area (SW Slovenia) was studied by using an indirect research method based on natural tracers. The variations of natural tracers (in precipitation and in groundwater) during the storm event made possible the separation of the Hubelj spring storm hydrograph by the three-component separation technique. The results produced information on the aquifer recharge, storage and discharge processes, as well as on the mechanisms that affected them. They verified the so-called epikarst hypothesis presuming that an important part of a karst aquifer recharge reaches rapidly and intensively from the epikarst zone. It was demonstrated that epikarst water could occupy up to 50% of the spring discharge during precipitation events. This phenomenon could have important consequences on protection and management of the problems of karst aquifers, including engineering problems in karst areas. With this respect the results could give way to new engineering ideas.  相似文献   

8.
《Applied Geochemistry》2000,15(6):791-805
This paper describes the geochemical evolution of groundwater in the Bathonian and Bajocian aquifer along its flowpath. Since this aquifer represents one of the main sources of fresh water supply in the Caen area and has been subjected to a Holocene marine intrusion, its management requires a sound knowledge of (1) the primary conditions and (2) the potential influence of either natural or anthropogenic pressures. Groundwater vertical sampling validity is discussed with the contribution of high resolution temperature logging. The main processes of geochemical evolution along a groundwater flow line and the sea-water intrusion characteristics are discussed using ionic concentrations (Br−, F− and major elements) and isotopes (water δ2H and δ18O, TDIC δ13C and A14C, sulphate δ18O and δ34S). As the 13C content of TDIC is used as a tracer of water-rock interaction, it shows evidence of specific chemical and isotopic evolutions of groundwater within the aquifer, both related to water-rock interaction and mineral equilibria in groundwater. All the above-mentioned tracers evolve downflow: cation concentrations are modified by exchange with clay minerals allowing a high F− concentration in groundwater, whereas Br− and SO2−4 concentrations appear to be redox condition dependant. Superimposed on these geochemical patterns, δ18O and δ2H compositions indicate that aquifer recharge has varied significantly through time. The chemical evolution of groundwater is locally affected by a salty water intrusion that is characterised by mixing between Flandrian fresh water and sea-water which has interacted with peat as evidenced by a high Br−/Cl− ratio and SO2−4 reduction.  相似文献   

9.
《Applied Geochemistry》1999,14(3):333-363
The hydrochemical, radiochemical, stable isotope, 14C and dissolved noble gas composition of groundwaters has been determined along two profiles across the confined, fissured Chalk aquifer of the London Basin of southern England, and for selected sites in the adjacent Berkshire Basin. During downgradient flow in the London Basin aquifer, the groundwater chemistry is modified by water–rock interactions: congruent and incongruent reaction of the carbonate lithology resulting in enhanced Mg/Ca and Sr/Ca ratios and 13C contents with increased residence times; redox and ion exchange reactions; and towards the centre of the Basin, mixing with a residual saline connate water stored in the Chalk matrix. There is evidence from anomalous water chemistries for a component of vertical leakage from overlying Tertiary beds into the confined aquifer as a result of historical dewatering of the aquifer. Dissolved noble gas contents indicate the climate was up to 4.5°C cooler than at present during recharge of the waters now found in the centres of both Basins; stable isotope (2H and 18O) depletions correspond to this recharge temperature change. For evolved waters having δ13C > −8‰ PDB a negative linear correlation is demonstrated between derived recharge temperatures and δ13C values, which is interpreted as mixing between relatively warm, light isotopic, fracture-borne waters and cooler stored waters of the matrix having a 13C signature more or less equilibrated with the Chalk. From geochemical (14C, 4He) age estimates, the abstracted water is interpreted as being either of wholly Holocene/post-Devensian glacial origin, or an admixture of Holocene and Late Pleistocene pre-glacial (cold stage interstadial) recharge. Devensian pleniglacial stage waters of the Last Glacial Maximum are not represented.  相似文献   

10.
《Applied Geochemistry》2003,18(7):1043-1063
The Memphis aquifer in southwestern Tennessee is confined to a semi-confined unconsolidated sand aquifer and is the primary municipal water source in the Memphis metropolitan area. Past studies have identified regions in the metropolitan area in which the overlying upper Claiborne confining unit lacks significant clay and provides a hydraulic connection between the shallow aquifer and the Memphis aquifer. In this study, major solute chemistry, 3H, and 3H/3He groundwater dating are used to investigate the extent and chemical effects of leakage through the confining unit to the Memphis aquifer in the vicinity of a municipal well field. The 3H/3He dates and geochemical modeling of the chemical data are used to constrain mixing fractions and the timing of modern recharge. Tritium activities of as much as 2.8 TU are observed in shallow production wells, but deeper production wells have 3H activities that approach the detection limit. Trends in water chemistry indicate vertical mixing in the aquifer of shallow Na–SO4–Cl-rich water and deeper Ca–Mg–HCO3-rich water. Water chemistry does not vary consistently with seasonal pumping, but 3H activity generally decreases during low use periods. Stable O and H isotopes show little variation and are not useful groundwater tracers for this study. The 3H-bearing, Na–SO4–Cl-rich water is interpreted to reflect recharge of modern water through the upper Claiborne confining unit. The 3H/3He dates from 5 production wells indicate modern recharge, that infiltrated 15–20 a ago, is present in the shallow production wells. Geologic data and hydrologic boundary conditions suggest that the most likely source for continued leakage is a nearby stream, Nonconnah Creek. Geochemical reaction modeling using the NETPATH computer code suggests that proportions of shallow aquifer water leaking into the Memphis aquifer range from 6 to 32%. The 3H/3He dating and NETPATH modeling results correlate well, suggesting that these complementary analytical tools provide an effective means to evaluate proportions of modern water leaking into semi-confined aquifers. These results also indicate a need to carefully consider connections between surface water and semi-confined groundwater resources in wellhead protection programs.  相似文献   

11.
《Applied Geochemistry》1998,13(6):735-749
Samples have been collected from inflows into railway tunnels in the Triassic sandstone aquifer beneath Liverpool and the Mersey Estuary, England, U.K. These provide a profile through a saline–freshwater mixing zone. Analyses were made of major anions and cations, δ34S and δ18O in SO4, δ13C in dissolved inorganic C and 87Sr/86Sr. The data demonstrate that the presence of a low permeability fault exerts a strong control on the local groundwater chemistry. On the estuary side of the fault, groundwater chemistry is dominated by mixing of intruding estuary water, which is modified by SO4 reduction and calcite dissolution, with fresh groundwater. The environment of SO4 reduction in the tidal estuary is one of repeated reduction and re-oxidation of S in an open system and has resulted in virtually no change in S isotopic composition, but an enrichment in residual SO4 δ18O of 1.5‰. Groundwater chemistry on the landward side of the fault is primarily the result of recharge in an urban environment. There is also evidence that saline water has been present in this region of the aquifer in the past and that this has now been flushed by fresh groundwaters. This saline water was either transported along the landward side of the fault from nearer the estuary or more probably transmitted across the fault. Both mechanisms would have been driven by large landward head gradients caused by heavy industrial abstraction earlier this century. This has produced a zone of groundwaters depleted in Ca and radiogenic Sr and enriched in Na as a result of ion exchange between the fresh groundwaters and the aquifer previously occupied by more saline water. Sulphur isotopic composition, however, shows no variation since SO4 does not undergo significant ion exchange. A tracer test from a borehole to the tunnels showed multiple breakthroughs to some locations indicating a number of different flow paths through the aquifer. The maximum flow velocity recorded in this test was 140 m/d suggesting flow along fractures.  相似文献   

12.
岩溶水系统的水化学曲线及其在水文地质研究中的应用   总被引：5，自引：0，他引：5  
为了认识水文地质条件与岩溶泉水化学之间的关系,以西南地区的6个典型岩溶水系统丫吉试验场S31号泉、毛村地下河、官村地下河、陈旗岩溶泉、青木关地下河以及金佛山水房泉为例进行研究。通过对比发现,在这些强烈非均质的山区裸露型岩溶水系统中,仪器能够实现自动化监测的电导率、温度和pH值等指标的水化学曲线存在差异。分析可知控制水化学变化的主要因素如下:首先是降雨补给引起系统的水量与碳酸盐岩溶解过程的变化;其次是CO2气体随降雨进入含水层,促进碳酸盐岩的溶解;最后是地表污染物的淋滤。当电导率、水温、pH曲线出现降低和碳酸盐岩矿物饱和指数下降时,反映的是岩溶水的稀释作用;当电导率曲线出现高峰时,反映的是岩溶水补给的CO2效应,此时水中二氧化碳分压(pCO2)升高;当场雨中水化学曲线的变化滞后于水文动态曲线时,反映的是岩溶管道的活塞流效应;与人类活动有关的NO3-等污染物质量浓度在降雨后出现高峰,反映土壤的降雨淋滤作用,并可能影响电导率的变化趋势。某个系统的水化学曲线趋向于经常出现某几种效应,并且彼此的类型不同,表明了降雨补给的面状渗流方式和集中灌入方式对岩溶水影响的强弱不同,以及系统在径流方式和调蓄机制上的差异。一般而言:以面状补给方式为主的系统,水化学曲线多表现为CO2效应,较少出现稀释作用;而岩溶发育强烈的系统,降雨补给受控于溶蚀裂隙和管道,其水化学曲线较多出现稀释作用,较少出现CO2效应;以管道为主要径流方式的系统易出现活塞流效应,而包气带厚度大和含水层储水能力强的系统水化学变化被减弱。  相似文献   

13.
This study aims to investigate the hydrochemical characteristics of shallow aquifer in a semi-arid region situated in northwest Algeria, and to understand the major factors governing groundwater quality. The study area is suffering from recurring droughts, groundwater resource over-exploitation and groundwater quality degradation. The approach used is a combination of traditional hydrochemical analysis methods of multivariate statistical techniques, principal component analysis (PCA), and ratios of major ions, based on the data derived from 33 groundwater samples collected in February 2014. Results show that groundwater in the study area are highly mineralized and collectively has a high concentration of chloride (as Cl?). The dominant water types are Na-Cl (27%), Mg-HCO3 (24%) and Mg-Cl (24%). According to the (PCA) approach, salinization is the main process that controls the hydrochemical variability. The PCA analysis reveal the impact of anthropogenic factor especially the agricultural activities on the groundwater quality. The PCA highlighted two types of recharge: Superficial recharge from effective rainfall and excess irrigation water distinguished by the presence of nitrate and lateral recharge or vertical leakage from carbonate formations marked by the omnipresence of HCO3?. Additionally, three categories of samples were identified: (1) samples characterized by good water quality and receiving notable recharge from carbonate formations; (2) samples impacted by the natural salinization process; and (3) samples contaminated by anthropogenic activities. The major natural processes influencing water chemistry are the weathering of carbonate and silicate rocks, dissolution of evaporite as halite, evaporation and cation exchange. The study results can provide the basis for local decision makers to ensure the sustainable management of groundwater and the safety of drinking water.  相似文献   

14.
Stable isotope data for the Hueco Bolson aquifer (Texas, USA and Chihuahua, Mexico) distinguish four water types. Two types relate to recharge from the Rio Grande: pre-dam (pre-1916) river water with oxygen-18 and deuterium (δ18O, δD, ‰) from (?11.9, ?90) to (?10.1, ?82), contrasts with present-day river water (?8.5, ?74) to (?5.3, ?56). Pre-dam water is found beneath the Rio Grande floodplain and Ciudad Juárez, and is mixed with post-dam river water beneath the floodplain. Two other types relate to recharge of local precipitation; evidence of temporal change of precipitation isotopes is present in both types. Recharge from the Franklin and Organ Mountains plots between (?10.9, ?76) and (?8.5, ?60) on the global meteoric water line (GMWL), and is found along the western side of the Hueco Bolson, north of the Rio Grande. Recharge from the Diablo Plateau plots on an evaporation trend originating on the GMWL near (?8.5, ?58). This water is found in the southeastern Hueco Bolson, north of the river; evaporation may be related to slow recharge through fine-grained sediment. Pre-dam water, recognizable by isotope composition, provides information on groundwater residence times in this and other dammed river basins.  相似文献   

15.
The quality of water in the Upper Floridan aquifer near Valdosta, Georgia is affected locally by discharge of Withlacoochee River water through sinkholes in the river bed. Data on transient tracers and other dissolved substances, including Cl−, 3H, tritiogenic helium-3 (3He), chlorofluorocarbons (CFC-11, CFC-12, CFC-113), organic C (DOC), O2 (DO), H2S, CH4, δ18O, δD, and 14C were investigated as tracers of Withlacoochee River water in the Upper Floridan aquifer. The concentrations of all tracers were affected by dilution and mixing. Dissolved Cl−, δ18O, δD, CFC-12, and the quantity (3H+3He) are stable in water from the Upper Floridan aquifer, whereas DOC, DO, H2S, CH4, 14C, CFC-11, and CFC-113 are affected by microbial degradation and other geochemical processes occurring within the aquifer. Groundwater mixing fractions were determined by using dissolved Cl− and δ18O data, recognizing 3 end-member water types in the groundwater mixtures: (1) Withlacoochee River water (δ18O=−2.5±0.3‰, Cl−=12.2±2 mg/l), (2) regional infiltration water (δ18O=−4.2±0.1‰, Cl−=2.3±0.1 mg/l), and (3) regional paleowater resident in the Upper Floridan aquifer (δ18O=−3.4±0.1‰, Cl−=2.6±0.1 mg/l) (uncertainties are ±1σ). Error simulation procedures were used to define uncertainties in mixing fractions. Fractions of river water in groundwater range from 0 to 72% and average 10%. The influence of river-water discharge on the quality of water in the Upper Floridan aquifer was traced from the sinkhole area on the Withlacoochee River 25 km SE in the direction of regional groundwater flow. Infiltration of water is most significant to the N and NW of Valdosta, but becomes negligible to the S and SE in the direction of general thickening of post-Eocene confining beds overlying the Upper Floridan aquifer.  相似文献   

16.
河水入渗路径和范围对确定地下水补给条件，以及水资源调控和合理利用有着重要意义。针对2015年以来怀柔地区地下水水位回升现象，开展了地下水动态影响因素研究，采集了河水和地下水样品，测试了水化学和氢氧稳定同位素组成。δD-δ18 O数据表明该区有河水入渗补给地下水，河流附近地下水为地下水与入渗河水的混合物。利用地下水δ18O值以及二元混合模型计算了地下水中入渗河水的比例，揭示出地下水中河水占比减小方向与地下水水力梯度下降方向一致；局部河段附近地下水Cl-含量增加，表明河水入渗会引起地下水水质变化。入渗河水影响范围的圈定为评价入渗河水对地下水的影响提供了重要数据。该项工作对理解研究区地下水水文过程、控制因素以及水资源管理具有指导意义。  相似文献   

17.
222Rn was used to assess river–groundwater interactions within Castel di Sangro alluvial aquifer (Italy). The effectiveness of results obtained through this indicator was verified by also analyzing δ18O, major ions and temperature in both surface and groundwater, and carrying out piezometric head monitoring and discharge measurements. Hydrogeological investigations suggested that the river infiltrates into the aquifer in the south-eastern aquifer portion, while groundwater discharges into the river in the north-eastern portion. The latter phenomenon is supported by 222Rn data. Nevertheless, flow-through conditions cause the modelled discharge along this river reach, estimated by 222Rn data in a degassing-corrected two-component mixing model, to be greater than the measured discharge. Concerning river infiltration into the aquifer, δ18O, major ions and temperature data show that the river contribution is negligible in terms of aquifer recharge. Thus, the observed increase in 222Rn concentration in that portion of the aquifer is due to the enrichment process caused by infiltration of rainwater (222Rn free) which flows from the local divide area. Hence, in the study site, the use of only 222Rn to predict river–groundwater interactions causes some estimation inaccuracies and it must be coupled with other hydrochemical and hydrogeological parameters to gain a thorough understanding of such interactions.  相似文献   

18.
《Applied Geochemistry》1998,13(4):463-475
Strontium isotope ratios were measured on 13 rock, 18 leachate and 28 pore-water samples from the Milk River aquifer, the confining argillaceous formations, and the glacial till mantling the recharge area. Strontium isotope ratios (87Sr/86Sr) of pore waters from the aquifer, confining units, and the glacial till ranged from 0.7069 to 0.7082. The 87Sr/86Sr ratios in aquifer pore waters decrease with increasing distance from the aquifer recharge area, and this is interpreted to be the result of mixing and water–rock interaction within the aquifer.The solute composition of the recharging groundwater is modified by the local lithology, causing distinct geochemical patterns along different flow paths within the aquifer. Whole-rock 87Sr/86Sr ratios indicate that the shales and till are generally more radiogenic than the aquifer sandstone. The authigenic carbonate cements and rock-forming minerals comprising the major lithologic units had little apparent influence on the pore-water Sr chemistry. Carbonate cement leachates from the till and the aquifer sandstone are more radiogenic than those from the confining shale formations. Feldspar separates from the aquifer sandstone have relatively radiogenic Sr isotope ratios, whereas bentonites from the Milk River and Colorado Shale Formations have whole-rock and leachate Sr isotope ratios that are relatively unradiogenic. Ratios of most Milk River aquifer pore waters are lower than those of any leachates or whole rocks analyzed, except the bentonites.The 87Sr/86Sr ratios of exchangeable Sr in the bentonites are similar to ratios found in the more evolved pore waters. Simple rock–water interaction models calculated for the whole-rock, leachate, and exchangeable-ion/pore-water pairs indicate that ion exchange with bentonite clays within the Milk River and Colorado Shale Formations appears to influence the isotopic evolution of the pore-water Sr in each of these units.  相似文献   

19.
High water demand for domestic use in Douala with over 3 million inhabitants is met mainly by shallow groundwater. Field measurements and water sampling in January 2015 were carried out to examine the major controls on the groundwater composition and spatial view of ions in the water, timing of recharge and link between the recharge process and quality of the water. Fifty-two water samples were analysed for major ions and stable hydrogen and oxygen isotopes. Low pH values (3.61–6.92) in the groundwater indicated an acidic aquifer; thus, prone to acidification. The dominant water type was Na–Cl. Nitrate, which exceeded the WHO guide value of 50 mg/l in 22% of the groundwater, poses a health problem. Mass ratios of Cl?/Br? in the water ranged from 54 to 3249 and scattered mostly along the mixing lines between dilute waters, septic-tank effluent and domestic sewage. A majority of the samples, especially the high NO3 ? shallow wells, clustered around the septic-tank effluent-end-member indicating high contamination by seepage from pit latrines; hence, vulnerable to pollution. Stable isotopes in the groundwater indicated its meteoric origin and rapid infiltration after rainfall. The δ18O values showed narrow ranges and overlaps in rivers, springs, open wells and boreholes. These observations depict hydraulic connectivity, good water mixing and a homogeneous aquifer system mainly receiving local direct uniform areal recharge from rainfall. The rapid and diffused recharge favours the leaching of effluent from the pit toilets into the aquifer; hence, the high NO3 ? and Cl? in shallow wells. Silicate weathering, ion exchange and leaching of waste from pit toilets are the dominant controls on the groundwater chemistry. Drilling of deep boreholes is highly recommended for good-quality water supply. However, due the hydraulic connection to the shallow aquifer, geochemical modelling of future effects of such an exploitation of the deeper aquifer should support groundwater management and be ahead of the field actions.  相似文献   

20.
Investigations in the Jiaozuo coal-mining district (China) aim to link water-inrush aquifers with the sources of groundwater recharge. Concentrations of TDS, HCO 3 – , Cl– and Na+ in the groundwater samples gradually decrease with increasing depth; in contrast, the factor 1 value of the Q-mode analysis gradually increases, which indicates that the deep groundwater may upflow, recharging the aquifers near the faulted zone. Some groundwater samples (above the local meteoric water line and ‘evaporation line 1’) may originate from recharge by infiltrating local rainfall. Spring and river samples are symmetrically distributed on the regression line of the Ordovician and Carboniferous limestone aquifer groundwater (δ2H?=?3.76?×?δ18O?–?31.77) and may, therefore, originate from groundwater recharge in the northern Taihang mountains. This mechanism is supported by the observation that groundwater levels change with rainfall. According to radiocarbon residence-time estimates, two groundwater sample sites may have been recharged during the late glacial stage.  相似文献   

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