A chlorine-36 study of regional groundwater flow and vertical transport in southern Nevada

Chlorine-36 data for groundwater from the Death Valley regional flow system is interpreted in the context of existing conceptual models for regional groundwater flow in southern Nevada. Chlorine-36 end member compositions are defined for both recharge and chemically evolved groundwater components. The geochemical evolution of ³⁶Cl is strongly controlled by water-rock interaction with Paleozoic carbonate rocks that comprise the regional aquifer system, resulting in chemically evolved groundwater that is characteristically low in ³⁶Cl/Cl and high in Cl. Groundwater from alluvial and volcanic aquifers that overlie the regional carbonate aquifer are generally characterized by high ³⁶Cl/Cl and low Cl signatures, and are chemically distinct from water in the regional carbonate aquifer. This difference provides a means of examining vertical transport and groundwater mixing processes. In combination with other geochemical and hydrogeologic data, the end members defined here provide constraints on aquifer residence times and mixing ratios.     

Geochemical tracing and hydrogeochemical modelling of water–rock interactions during salinization of alluvial groundwater (Upper Rhine Valley,France)

In the southern Upper Rhine Valley, groundwater has undergone intensive saline pollution caused by the infiltration of mining brines, a consequence of potash extraction carried out during the 20th century. Major and trace elements along with Sr and U isotopic ratios show that groundwater geochemical characteristics along the saline plumes cannot reflect conservative mixing between saline waters resulting from the dissolution of waste heaps and one or more unpolluted end-members. The results imply the occurrence of interactions between host rocks and polluted waters, and they suggest that cationic exchange mechanisms are the primary controlling process. A coupled hydrogeochemical model has been developed with the numerical code KIRMAT, which demonstrates that cationic exchange between alkalis from polluted waters and alkaline-earth elements from montmorillonite present in the host rock of the aquifer is the primary process controlling the geochemical evolution of the groundwater. The model requires only a small amount of montmorillonite (between 0.75% and 2.25%), which is in agreement with the observed mineralogical composition of the aquifer. The model also proves that a small contribution of calcite precipitation/dissolution takes places whereas other secondary mineral precipitation or host rock mineral dissolution do not play a significant role in the geochemical signature of the studied groundwater samples. Application of the model demonstrates that it is necessary to consider the pollution history to explain the important Cl, Na and Ca concentration modifications in groundwater samples taken over 2 km downstream of waste heaps. Additionally, the model shows that the rapidity of the cationic exchange reactions insures a reversibility of the cation fixation on clays in the aquifer.     

The recharge of glacial meltwater and its influence on the geochemical evolution of groundwater in the Ordovician-Cambrian aquifer system,northern part of the Baltic Artesian Basin

The geochemical evolution of groundwater in the Ordovician-Cambrian aquifer system in the northern part of the Baltic Artesian Basin (BAB) illustrates how continental glaciations have influenced groundwater systems in proglacial areas. The aquifer system contains water that has originated from various end-members: recent meteoric water, glacial meltwater and relict Na-Cl brine. The saline formation water that occupied the aquifer system prior to the glacial meltwater intrusion has been diluted by meltwaters of advancing-retreating ice sheets. The diversity in the origin of groundwater in the aquifer system is illustrated by a wide variety in δ¹⁸O values that range from −11‰ to −22.5‰. These values are mostly depleted with respect to values found in modern precipitation in the area. The chemical and isotopic composition of groundwater has been influenced by mixing between waters originating from different end-members. In addition, the freshening of a previously saline water aquifer due to glacial meltwater intrusion has initiated various types of water-rock interaction (e.g. ion exchange, carbonate mineral dissolution).     

Hydrogeologic controls on groundwater recharge and salinization: a geochemical analysis of the northern Hueco Bolson aquifer, Texas, USA

Identification of hydrogeologic controls on groundwater flowpaths, recharge, and salinization is often critical to the management of limited arid groundwater resources. One approach to identifying these mechanisms is a combined analysis of hydrogeologic and hydrochemical data to develop a comprehensive conceptual model of a groundwater basin. To demonstrate this technique, water samples were collected from 33 discrete vertical zone test holes in the Hueco Bolson aquifer, located within the Trans-Pecos Texas region and the primary water resource for El Paso, Texas, USA and Juárez, Mexico. These samples were analyzed for a suite of geochemical tracers and the data evaluated in light of basin hydrogeology. On the basis of δ²H and δ¹⁸O data, two regional recharge sources were recognized, one originating from western mountain-fronts and one from through-flow of the adjacent Tularosa aquifer. Chloride concentrations were strongly correlated with lithologic formations and both Cl/Br and ³⁶Cl ratios suggested the primary chloride source is halite dissolution within a specific lithologic unit. In contrast, sulfur isotopes indicated that most sulfate originates from Tularosa basin Permian gypsum sources. These results yielded a more comprehensive conceptual model of the basin, which suggested that chloride salinization of wells is the result of upconing of waters from the Fort Hancock formation.     

Isotope measurements and ground water flow modeling using MODFLOW for understanding environmental changes caused by a well field in semiarid Brazil

Measurements of the environmental isotopes carbon-14 and oxygen-18 and of the electrical conductivity in ground water, together with MODFLOW-88 (DOS) simulations of pumping tests, were used to achieve a detailed understanding of the functioning of an aquifer in the area of a well field. The methodology was applied in the sedimentary basin of the Cariri region, in the south of Ceará State in Brazil. Localized hydraulic connections between adjacent aquifer units could be detected, and mixing ratios for the contributions from the units involved were determined. Cone of depression simulations for a three-year drought period revealed well interference and a drastic lowering of the piezometric level, thereby explaining the hydrogeologic changes and transformations in vegetation that were observed in the area of the well field. The combined use of the modeling tools and the geochemical field observations is shown to provide more detailed insight into the conceptual model of the groundwater flow system.     

Hydrogeochemistry of groundwaters in a semi-arid region. El Ma El Abiod aquifer, Eastern Algeria

In this work, we present results of the hydrogeochemical and isotopic studies on groundwater samples from the El Ma El Abiod Sandstone aquifer, in Tébessa, Algeria. Chemical and environmental isotope data are presented and discussed in order to identify the geochemical processes and their relation with groundwater quality as well as to get an insight into the hydrochemical evaluation, in space and time, of groundwater and of the origin of dissolved species. A combined hydrogeologic and isotopic investigation have been carried out using chemical and isotopic data to deduce a hydrochemical evaluation of the aquifer system based on the ionic constituents, water types, hydrochemical facies, and factors controlling groundwater quality. All of the investigated groundwaters are categorized into two chemical types: low mineralized water type and relatively high mineralized water type. Interpretation of chemical data, based on thermodynamic calculations and geochemical reaction models of selected water groups constructed using PHREEQC, suggest that the chemical evolution of groundwater is primarily controlled by water–rock interactions, involving (1) acidic weathering of aluminosilicates, (2) dissolution of secondary carbonate minerals, and (3) cation exchange of Na⁺ for Ca²⁺. However, the original composition of groundwater may have been modified by further secondary processes such as mixing of chemically different water masses. The combined use of SI and mass-balance modeling has shown to be a useful approach in interpreting groundwater hydrochemistry in an area where large uncertainties exist in the understanding of the groundwater flow system. Interpretation of ¹⁸O and ²H, suggest that the recharge of the investigated groundwaters may result from different mechanisms.     

Desalination of a sedimentary rock aquifer system invaded by Pleistocene Champlain Sea water and processes controlling groundwater geochemistry

The objective of this study was to identify geochemical processes and Quaternary geological events responsible for the variations in groundwater geochemistry observed in a sedimentary rock aquifer system, including brackish to saline groundwater. Inorganic constituents and environmental isotopes were analyzed for 146 groundwater samples. Dissolution of carbonates dominates in recharge areas, resulting in Ca-, Mg-HCO₃ groundwater. Further along flow paths, under confined conditions, Ca²⁺–Na⁺ ion exchange causes groundwater evolution to Na-HCO₃ type. Na-Cl groundwater is also found and it falls on a seawater mixing line. Using conservative tracers, Cl⁻ and Br⁻, the original Champlain Sea water is shown to have been, in the region, a mixture of about 34% seawater and 66% freshwater, a composition still retained by some groundwater. Na-Cl groundwater thus results from mixing with former Champlain Sea water and also from solute diffusion from overlying marine clay. The system is thus found to be at different stages of desalinization, from the original Champlain Sea water still present in hydraulically stagnant areas of the aquifer to fully flushed conditions in parts, where more flow occurs, especially in recharge zones. The geochemical processes are integrated within the hydrogeological context to produce a conceptual geochemical evolution model for groundwater of the aquifer system.     

地下水中微量组份H2SiO3富集的地质地球化学环境

通过对全国325处富含偏硅酸地下水点的化学测试数据、所处的地球化学环境、地质背景的分析,阐述了微量组份H2SiO3的富集特征与含水介质岩性的关系,以及富含H2SiO3地下水的地球化学特征。认为富含H2SiO3地下水的形成与不同含水介质岩性和SiO2平均丰度等地球化学环境密切相关。地下水中H2SiO3富集的最有利地质环境是中酸性侵入岩地层,其次是区域变质岩、喷出岩、碎屑岩。研究表明,地下水中的H2SiO3含量与水化学类型和pH值相关,推断出HCO3-Ca、HC03-CaNa型水和碱性、酸性水都有利于H2Si03的富集。     

Hydrochemistry and origins of mineralized waters in the Puebla aquifer system,Mexico

Significant upward movement of mineralized water takes place in the Puebla aquifer system. Preferential groundwater flow paths related to the geological structure and the lowering of the potentiometric surface are suspected to be the prime factors for this intrusion. A combined approach of geochemical and isotope analyses was used to assess the sources of salinity and processes that are controlling the changes in groundwater chemical composition in the Puebla aquifer. Geochemical and isotope data indicate that the likely source of increased solutes is mineralized water from the dissolution of evaporites of the Cretaceous age at the base of the Upper deep aquifer, which is deeper than the intakes of the shallow wells. Dedolomitization and cation exchange seems also to occur along flow paths where sulphate concentrations tend to increase. The deep regional flow paths controls the chemical stratification of groundwater in response to decreased heads through interconnecting vertical and horizontal pathways, such as in the Fosa Atlixco. The results also suggest that high sulphate concentrations originating in the Lower deep aquifer are currently affecting shallow production wells. It is concluded that hydrodynamic aspects together with hydrogeochemical characteristics need to be taken into account to correctly explain the hydrochemical evolution in the stratified aquifer.     

Geochemistry of regional aquifer systems hosted by carbonate-evaporite formations in Umbria and southern Tuscany (central Italy)

In central Italy Mesozoic carbonates represent the principal reservoir of freshwater of the region. The hydrogeological setting is linked to the geological evolution of the Apennine chain and is generally characterised by a lower aquifer and one or more shallower aquifers separated by thin aquicludes. In these systems, groundwater composition is the result of a complex array of regional and local geochemical processes. The main geochemical processes are the dissolution of calcite, the influx of deeply derived CO₂ related to a regional process of mantle degassing, dedolomitization and mixing with deep saline fluids. The occurrence of saline fluids, characterised by a Na–Cl(HCO₃) composition, is related to the presence of a deep regional aquifer at the base of Mesozoic carbonates. The extremely high pCO₂ values computed for the saline waters suggest that the deep aquifer is also a structural trap for the mantle derived CO₂ during its ascent towards the surface. In central Italy, geological and geophysical data highlight the presence of two different crustal sectors: the eastern sector, where the geometry of the Apennine thrust belt is still preserved, and the western sector, where the compressive structures are dislocated by important extensional deformations. In the western sector, the normal faults disrupting the compressive structures allow the mixing of the deep Na–Cl(HCO₃) fluids with the shallow groundwater causing a salinity increase and the natural deterioration of groundwater quality.     

Numerical groundwater-flow modeling to evaluate potential effects of pumping and recharge: implications for sustainable groundwater management in the Mahanadi delta region,India

Process-based groundwater models are useful to understand complex aquifer systems and make predictions about their response to hydrological changes. A conceptual model for evaluating responses to environmental changes is presented, considering the hydrogeologic framework, flow processes, aquifer hydraulic properties, boundary conditions, and sources and sinks of the groundwater system. Based on this conceptual model, a quasi-three-dimensional transient groundwater flow model was designed using MODFLOW to simulate the groundwater system of Mahanadi River delta, eastern India. The model was constructed in the context of an upper unconfined aquifer and lower confined aquifer, separated by an aquitard. Hydraulic heads of 13 shallow wells and 11 deep wells were used to calibrate transient groundwater conditions during 1997–2006, followed by validation (2007–2011). The aquifer and aquitard hydraulic properties were obtained by pumping tests and were calibrated along with the rainfall recharge. The statistical and graphical performance indicators suggested a reasonably good simulation of groundwater flow over the study area. Sensitivity analysis revealed that groundwater level is most sensitive to the hydraulic conductivities of both the aquifers, followed by vertical hydraulic conductivity of the confining layer. The calibrated model was then employed to explore groundwater-flow dynamics in response to changes in pumping and recharge conditions. The simulation results indicate that pumping has a substantial effect on the confined aquifer flow regime as compared to the unconfined aquifer. The results and insights from this study have important implications for other regional groundwater modeling studies, especially in multi-layered aquifer systems.     

The hydrogeology of the Ballimore region,central New South Wales,Australia: an integrated study

The integrated use of geophysical, geological, hydrogeochemical and hydrogeological data has allowed the development of a plausible conceptual model for groundwater flow in the Ballimore region. A realistic model for this under-explored system could not be derived solely by the use of hydrogeological data. Interpretation of the available datasets indicates that two groundwater systems are active: a regional and a local system. These are separated by a regionally extensive aquiclude. Groundwater flow in the regional groundwater system is controlled by the structural fabric of the Palaeozoic basement rocks. The local groundwater system is restricted to the Permian to Recent sequence of cover rocks. The local groundwater system is subdivided into three cells: the deep, intermediate and shallow cells. Groundwater flow within the deep cell of the local groundwater system is controlled by fracture flow. Groundwaters from this aquifer are under artesian pressure and are effervescent (CO₂-gas). The intermediate cell is a leaky aquitard that acts as a mixing zone between the deep and shallow cells. Groundwater flow within the shallow cell is controlled by the influx of surface waters which migrate laterally through permeable beds.     

Using non-conservative tracers to characterise karstification processes in the Merinos-Colorado-Carrasco carbonate aquifer system (southern Spain)

The systematic sampling of the chemical composition of the groundwater from five karst springs (including an overflow spring) and one outflowing borehole have permitted to determine distinctive chemical changes in the waters that reflect the geochemical processes occurring in a carbonate aquifer system from southern Spain. The analysis of the dissolution parameters revealed that geochemical evolution of the karst waters basically depends on the availability of the minerals forming aquifer rocks and the residence time within the aquifers. In the three proposed scenarios in the aquifers, which include the preferential flow routines, the more important geochemical processes taking place during the groundwater flow from the recharge to the discharge zones are: CO₂ dissolution and exsolution (outgassing), calcite net dissolution, calcite and dolomite sequential dissolution, gypsum/anhydrite and halite dissolution, de-dolomitization and calcite precipitation. A detailed analysis of the hydrochemical data set, saturation indices of the minerals and partial pressure of CO₂ in the waters joined to the application of geochemical modelling methods allowed the elaboration of a hydrogeochemical model of the studied aquifers. The developed approach contributes to a better understanding of the karstification processes and the hydrogeological functioning of carbonate aquifers, the latter being a crucial aspect for the suitable management of the water resources.     

人工回灌条件下多组分溶质的反应迁移模拟

人工回灌技术在我国水资源管理中占据重要地位,但是其实施对地下水环境质量也造成了较大的影响。如何保障人工回灌条件下地下水环境质量的安全稳定性,已成为人工回灌技术发展的瓶颈。以上海市某人工回灌试验场为例,结合试验场的地质、水文地质勘探结果,以TOUGHREACT为数值模拟平台,模拟预测人工回灌条件下地下水中多组分溶质的迁移转化过程。模拟结果表明：地下水化学成分主要受混合作用、阳离子交换吸附作用及含水层矿物相溶解-沉淀作用等影响;含水介质中石英、白云石、钾长石、钠长石及蒙脱石发生溶解,方解石发生沉淀,伊利石与高岭石则先溶解后沉淀,但各矿物相反应量极其微弱;按不同压力方案回灌,水位恢复速率随压力增大而加快,但地下水中化学成分变化趋势几乎不受压力影响。     

Source of salinity in the groundwater of Lenjanat Plain,Isfahan, Iran

The present study aimed at identifying the salinity source in the groundwater of Lenjanat Plain. To do so, non-isotopic geochemical methods were employed: groundwater samples were collected seasonally from 33 wells widespread in the area, and physicochemical parameters as well as major and minor elements were measured in the 132 samples. The data collected from the field and laboratory measurements were interpreted through statistical and hydrogeochemical graphs, mass ratios and saturation indexes obtained from modeling. The results revealed that hydrogeochemical properties of the study aquifer were controlled by rock/water interactions including ion exchange, dissolution of evaporation deposits (halite and gypsum) and precipitation/dissolution of carbonates. Based on the values of Cl/Br ratio in Lenjanat groundwater (329–4,492), dissolution of evaporation deposits in aquifer was the main cause for groundwater salinity. Considering the Lenjanat groundwater geochemical properties, the data confirm the reported Cl/Br ratios for groundwater affected by the dissolution of evaporation deposits (Cl/Br > 300) and overlaps with the range of Cl/Br ratios for domestic sewage effluent groundwater. Selecting the best chemical components and their ratios in non-isotopic geochemical methods provides an accurate distinction between sources of groundwater salinity.     

Characterization of the hydrogeologic environment at a petroleum hydrocarbon contaminated site in Korea

The hydrogeologic environment of a petroleum hydrocarbon contaminated site in Korea is characterized by hydrogeologic field work and chemical analyses of groundwater. Quaternary alluvium is the main aquifer contaminated by petroleum hydrocarbons, mainly TEX (toluene, ethylbenzene and xylenes). Contamination at this site was derived from the leaking of petroleum storage tanks. The aquifer is highly permeable, but vertically heterogeneous. Water-table fluctuations reach up to 2 m during heavy rains. Contaminants migrated to the northwest along the main groundwater-flow direction. The concentration of hydrocarbons in groundwater is particularly high downgradient from the source area. The ubiquitous distribution of TEX was caused by the heterogeneity of the aquifer material and the significant fluctuation of the water-table. Chemical properties of the contaminated groundwater and field parameters indicate that intrinsic biodegradation, including aerobic respiration, nitrate reduction, iron reduction, manganese reduction, and sulfate reduction, occurs at this site. The dilution and mixing due to new groundwater recharge from rainfall is also identified as one of the major attenuation processes of TEX.     

Sensitivity and uncertainty analysis of mixing and mass balance calculations with standard and PCA-based geochemical codes

One of the most important observations that can be obtained from the study of an aquifer system dominated by mixing is the contribution of each end-member water to the chemical composition of every water parcel in the aquifer. Once the first-order effect of mixing has been taken into account via the mixing proportions, water–rock interaction can be used to explain the remaining variability. There are many sources of uncertainty that can prevent the accurate calculation of the mixing proportions of a mixing-dominated system, but the type and intensity of the chemical reactions that have taken place as a consequence of mixing is one of the most critical. Here the uncertainty in the computed mixing proportions of samples from a “synthetic” aquifer system derived from the actuation of different chemical reactions are assessed (always remembering that the chemical reactions are a second-order effect). These uncertainties are explored using two different geochemical codes in order to infer the limits of both methodological approaches: PHREEQC, as an example of a standard geochemical code; and M3, as an example of a Principal Component-based geochemical code. Several synthetic water samples are created with the direct approach of PHREEQC, both by pure mixing and including different types of chemical reactions. Together with the chemical information of the end-member waters, these samples are then fed into PHREEQC (inverse modelling) and M3 and the mixing proportions and mineral mass transfers are computed. PHREEQC calculations give a reasonable estimate of the real mixing proportions and the chemistry of the groundwaters. However, similar mixing proportions and mass transfers can be obtained using different sets of reactions, indicating a source of uncertainty that should be overcome with additional chemical information. For M3, where synthetic samples have been included in a real data set of groundwater samples from the Scandinavian Shield, mixing proportions are only mildly affected either by the number of compositional variables or the number of samples used for the Principal Component Analysis (PCA). However, the robustness of the output is quite sensitive to whether only conservative compositional variables are used or both conservative and non-conservative compositional variables. Mass balance calculations in M3 are much more sensitive to non-conservative compositional variables and the recommendation here is not to use non-conservative variables with PCA-based codes if any information about reactions is to be obtained.     

Characterization of the groundwater flow system in the hillside and coastal aquifers of the Mersin-Tarsus region (Turkey)

In the region between Mersin and Tarsus cities, located along the Mediterranean Sea coast in southern Turkey, the demand for groundwater has increased dramatically as the available surface water supplies have already been developed. Fundamental information is required to characterize the existing groundwater system in this area in order to establish a sustainable groundwater-use policy. For this purpose, hydrochemical and environmental isotopic data were collected and integrated with available geological and hydrogeological information to develop a conceptual model of the system. Results, backed up mainly by depleted stable isotope composition and infinitesimal tritium content, suggest that most of the groundwater along the coastal zone is supplied by the neighboring mountain belt while local precipitation has also contributes to aquifer recharge. The validation of the conceptual perspective by a steady-state numerical groundwater flow model reveals that about 90% of the recharge to the aquifer system is supplied by the deep flow of karstic groundwater fed from the Taurus Mountains. Monitoring of changes in the recharge regime of the mountain sector seems to be critical in establishing future groundwater use policies.     

Origin of groundwater salinity (current seawater vs. saline deep water) in a coastal karst aquifer based on Sr and Cl isotopes. Case study of the La Clape massif (southern France)

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 (Cl_Ref. and Cl_Ref.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 Cl_Ref concentration. Group B includes groundwater with Cl⁻ concentrations that range between the Cl_Ref and Cl_Ref.Max concentrations. Group C includes brackish groundwater with Cl⁻ concentrations that are significantly greater than the Cl_Ref.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/Cl_molar 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.     

The integrated impacts of natural processes and human activities on groundwater salinization in the coastal aquifers of Beihai,southern China

Salinization in coastal aquifers is usually related to both seawater intrusion and water–rock interaction. The results of chemical and isotopic methods were combined to identify the origin and processes of groundwater salinization in Daguansha area of Beihai, southern China. The concentrations of the major ions that dominate in seawater (Cl^?, Na⁺, Ca²⁺, Mg²⁺ and SO ₄ ^2– ), as well as the isotopic content and ratios (²H, ¹⁸O, ⁸⁷Sr/⁸⁶Sr and ¹³C), suggest that the salinization occurring in the aquifer of the coastal plain is related to seawater and that the prevailing hydrochemical processes are evaporation, mixing, dissolution and ion exchange. For the unconfined aquifer, groundwater salinization has occurred in an area that is significantly influenced by land-based sea farming. The integrated impacts of seawater intrusion from the Beibuwan Gulf and infiltration of seawater from the culture ponds are identified in the shallowest confined aquifer (I) in the middle of the area (site BBW2). Leakage from this polluted confined aquifer causes the salinization of groundwater in the underlying confined aquifer (II). At the coastal monitoring site (BBW3), confined aquifer I and lower confined aquifer II are heavily contaminated by seawater intrusion. The weak connectivity between the upper aquifers, and the seaward movement of freshwater, prevents saltwater from encroaching the deepest confined aquifer (III). A conceptual model is presented. Above all, understanding of the origin and processes of groundwater salinization will provide essential information for the planning and sustainable management of groundwater resources in this region.