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1.
The study area is located on the western part of the alluvium‐filled gap between the Rajmahal hills on the west and the Garo hills on the east. Groundwater occurs under unconfined condition in a thick zone of saturation within the Quaternary alluvial sediments. Three hydrochemical facies with distinct characteristics have been identified which are dominated in general by alkaline earths and weak acids. The major‐ion chemistry of the area is controlled by weathering of silicate minerals, rainfall recharge, ion‐exchange processes and anthropogenic activities such as irrigation return flow and the application of inorganic fertilizers and pesticides. A stoichiometric approach suggests that mineral dissolution and anthropogenic activities contribute 79% and 21% of the total cations dissolved in groundwater. Principal component analysis (PCA) of 42 groundwater samples using 13 chemical parameters indicates that the combined processes of recharge of groundwater from rainfall, sediment water interaction, groundwater flow, infiltration of irrigation return water (which is arsenic rich due to the use of arsenic‐bearing pesticides, wood preservatives, etc. and the pumping of arsenic‐rich groundwater for agriculture purpose), oxidation of natural or anthropogenic organic matter and the reductive dissolution of ferric iron and manganese oxides play a key role in the evolution of groundwater in the study area. Factor 2 scores, associated with the infiltration of irrigation return water and spatial distribution of arsenic concentration reveal that the groundwater of the municipal area will not be affected by arsenic in the future in spite of heavy groundwater abstraction. Another PCA with geologic, geomorphic, anthropogenic, geochemical and landuse factors indicates that arsenic concentration in groundwater increases with increasing area of mango orchards, sand lithofacies and nitrate and decreases with increasing distance of paleochannel from the monitored well and depth of bore wells. High loading on nitrate may be attributed to the use of fertilizer, pesticides, etc. in mango orchards and agricultural land. High loadings on log pCO2, mango orchards (with negative sign) and phosphate (with positive sign) indicate that mango orchards provide the organic waste material which is decomposed to form organic carbon. The organic carbon undergoes oxidative carbon degeneration by different oxidants and increases the concentration of CO2 in the aquifer. The reducing condition thus developed in the aquifer helps to dissolve the arsenic adsorbed on iron hydroxide or oxy‐hydroxide coated margins of sand, iron rich heavy mineral grain margins, clay minerals and Fe–Mn concretions present in the aquifer matrix. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

2.
The impacts of long-term pumping on groundwater chemistry remain unclear in the Manas River Basin, Northwest China. In this study, major ions within five surface water and 105 groundwater samples were analyzed to identify hydrogeochemical processes affecting groundwater composition and evolution along the regional-scale groundwater flow paths using the multivariate techniques of hierarchical cluster analysis (HCA) and principal components analysis (PCA) and traditional graphical methods for analyzing groundwater geochemistry. HCA classified the groundwater samples into four clusters (C1 to C4). PCA reduced the dimensionality of geochemical data into three PCs, which explained 86% of the total variance. The results of HCA and PCA were used to identify three zones: “recharge,” “transition,” and “discharge.” In the recharge zone the groundwater type is Ca-HCO3-SO4 and is primarily impacted by the dissolution of calcite and silicate weathering. In the transition zone the groundwater type is Ca-HCO3-SO4-Cl and is impacted by rock dissolution and reverse ion exchange. In the discharge zone the groundwater type is Na-Cl and is impacted by evaporation and reverse ion exchange. In addition, anthropogenic activities impact the groundwater chemistry in the study area. The groundwater type generally changes from Ca-HCO3-SO4 in the recharge area to Na-Cl in the discharge area along the regional-scale groundwater flow paths. This study provides a process-based knowledge for understanding the interaction of groundwater flow patterns and geochemical evolution within the Manas River Basin.  相似文献   

3.
Flow regulation and water diversion for irrigation have considerably impacted the exchange of surface water between the Murray River and its floodplains. However, the way in which river regulation has impacted groundwater–surface water interactions is not completely understood, especially in regards to the salinization and accompanying vegetation dieback currently occurring in many of the floodplains. Groundwater–surface water interactions were studied over a 2 year period in the riparian area of a large floodplain (Hattah–Kulkyne, Victoria) using a combination of piezometric surface monitoring and environmental tracers (Cl−, δ2H, and δ18O). Despite being located in a local and regional groundwater discharge zone, the Murray River is a losing stream under low flow conditions at Hattah–Kulkyne. The discharge zone for local groundwater, regional groundwater and bank recharge is in the floodplain within ∼1 km of the river and is probably driven by high rates of transpiration by the riparian Eucalyptus camaldulensis woodland. Environmental tracers data suggest that the origin of groundwater is principally bank recharge in the riparian zone and a combination of diffuse rainfall recharge and localized floodwater recharge elsewhere in the floodplain. Although the Murray River was losing under low flows, bank discharge occurred during some flood recession periods. The way in which the water table responded to changes in river level was a function of the type of stream bank present, with point bars providing a better connection to the alluvial aquifer than the more common clay‐lined banks. Understanding the spatial variability in the hydraulic connection with the river channel and in vertical recharge following inundations will be critical to design effective salinity remediation strategies for large semi‐arid floodplains. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

4.
The Maqarin site in Jordan has been investigated for three decades as a natural analogue for the long term changes of materials in contact with hyper-alkaline solutions. Similar processes are expected in radioactive waste disposal sites, where cement based materials are in contact with natural rocks or other e.g. clay based materials. In this context, a numerical reactive transport model was used to study local geochemical alterations and induced porosity changes for the Maqarin marl rock in contact with the hyper-alkaline solution. The geochemical setup for the rock mineralogy and the pore water was calibrated to match measurements from the Maqarin site. The setup includes several clay and zeolite minerals, considers cation exchange processes, and a state-of-the-art model for cement phases. Similar to earlier calculations by Steefel and Lichtner (1998) who used a much simpler geochemical model, the pore clogging occurred after several hundred years at a distance of 5–10 mm from the contact to the hyper-alkaline solution. In our calculations, this was caused by a massive precipitation of ettringite and C–S–H minerals. We performed a sensitivity study by varying the intrinsic diffusion coefficient, the Archie’s law exponential factor, and the mineral surface area available for dissolution and precipitation. We found that the dissolution of clay minerals controls the availability of Al, which is needed for ettringite and C–S–H phase precipitation. Thus, the amount and kinetically controlled dissolution of clay minerals controls the spatial and temporal evolution of porosity changes. The simulations reveal that neither cation exchange processes nor the formation of zeolite minerals strongly influence the geochemical evolution of the system.  相似文献   

5.
Stable isotopic (δDVSMOW and δ18OVSMOW) and geochemical signatures were employed to constrain the geochemical evolution and sources of groundwater recharge in the arid Shule River Basin, Northwestern China, where extensive groundwater extraction occurs for agricultural and domestic supply. Springs in the mountain front of the Qilian Mountains, the Yumen‐Tashi groundwater (YTG), and the Guazhou groundwater (GZG) were Ca‐HCO3, Ca‐Mg‐HCO3‐SO4 and Na‐Mg‐SO4‐Cl type waters, respectively. Total dissolved solids (TDS) and major ion (Mg2+, Na+, Ca2+, K+, SO42?, Cl? and NO3?) concentrations of groundwater gradually increase from the mountain front to the lower reaches of the Guazhou Basin. Geochemical evolution in groundwater was possibly due to a combination of mineral dissolution, mixing processes and evapotranspiration along groundwater flow paths. The isotopic and geochemical variations in melt water, springs, river water, YTG and GZG, together with the end‐member mixing analysis (EMMA) indicate that the springs in the mountain front mainly originate from precipitation, the infiltration of melt water and river in the upper reaches; the lateral groundwater from the mountain front and river water in the middle reaches are probably effective recharge sources for the YTG, while contribution of precipitation to YTG is extremely limited; the GZG is mainly recharged by lateral groundwater flow from the Yumen‐Tashi Basin and irrigation return flow. The general characteristics of groundwater in the Shule River Basin have been initially identified, and the results should facilitate integrated management of groundwater and surface water resources in the study area. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

6.
Fractured rock aquifers cover much of Earth's surface and are important mountain sites for groundwater recharge but are poorly understood. To investigate groundwater systematics of a fractured-dominated aquifer in Baja California Sur, Mexico, we examined the spatial patterns of aquifer recharge and connectivity using the geochemistry of springs. We evaluate a range of geochemical data within the context of two endmember hypotheses describing spatial recharge patterns and fracture connectivity. Hypothesis 1 is that the aquifer system is segmented, and springs are fed by local recharge. Hypothesis 2 is that the aquifer system is well connected, with dominant recharge occurring in the higher elevations. The study site is a small <15 km2 catchment. Thirty-four distinct springs and two wells were identified in the study area, and 24 of these sites were sampled for geochemical analyses along an elevation gradient and canyon transect. These analyses included major ion composition, trace element and strontium isotopes, δ18O and δ2H isotopes, radiocarbon, and tritium. δ18O and δ2H isotopes suggest that the precipitation feeding the groundwater system has at least two distinct sources. Carbon isotopes showed a change along the canyon transect, suggesting that shorter flowpaths feed springs in the top of the transect, and longer flowpaths discharge near the bottom. Geochemical interpretations support a combination of the two proposed hypotheses. Understanding of the connectivity and provenance of these springs is significant as they are the primary source of water for the communities that inhabit this region and may be impacted by changes in recharge and use.  相似文献   

7.
Abstract

In order to evaluate groundwater quality and geochemical reactions arising from mixing between seawater and dilute groundwater, we performed a hydrochemical investigation of alluvial groundwater in a limestone-rich coastal area of eastern South Korea. Two sites were chosen for comparison: an upstream site and a downstream site. Data of major ion chemistry and ratios of oxygen–hydrogen isotopes (δ18O, δD) revealed different major sources of groundwater salinity: recharge by sea-spray-affected precipitation in the upstream site, and seawater intrusion and diffusion zone fluctuation in the downstream site. The results of geochemical modelling showed that Ca2+ enrichment in the downstream area is caused by calcite dissolution enhanced by the ionic strength increase, as a result of seawater–groundwater mixing under open system conditions with a constant PCO2 value (about 10?1.5 atm). The results show that, for coastal alluvial groundwater residing on limestone, significant hydrochemical change (especially increased hardness) due to calcite dissolution enhanced by seawater mixing should be taken into account for better groundwater management. This process can be effectively evaluated using geochemical modelling.

Editor D. Koutsoyiannis; Associate editor Y. Guttman

Citation Chae, G.-T., Yun, S.-T., Yun, S.-M., Kim, K.-H., and So, C.-S., 2012. Seawater–freshwater mixing and resulting calcite dissolution: an example from a coastal alluvial aquifer in eastern South Korea. Hydrological Sciences Journal, 57 (8),1–12.  相似文献   

8.
The hydrogeochemistry of shallow groundwater has been characterized in the Allt a'Mharcaidh catchment in the Scottish Cairngorms in order to: (i) assess the spatial and temporal variation in groundwater chemistry; (ii) identify the hydrogeochemical processes regulating its evolution; and (iii) examine the influence of groundwater on the quality and quantity of stream flow. Shallow groundwater in superficial drift deposits is circumneutral (pH∽7·1) and base cation concentrations are enriched compared with precipitation and drainage water from overlying podzolic soils. Modelling with NETPATH suggests that the dominant geochemical processes that account for this are the dissolution of plagioclase, K-feldspar and biotite. Groundwater emerging as springs from weathered granite underlying high altitude (>900 m) alpine soils shows similar characteristics, though weathering rates are lower, probably as a result of reduced residence times and lower temperatures. Chemical hydrograph separation techniques using acid neutralizing capacity (ANC) and Si as tracers show that groundwater is the dominant source of baseflow in the catchment and also buffers the chemistry of stream water at high flows: groundwater may account for as much as 50–60% of annual runoff in the catchment. Climate and land use in the Cairngorms are vulnerable to future changes, which may have major implications for hydrogeological processes in the area. © 1998 John Wiley & Sons, Ltd.  相似文献   

9.
Emerging groundwater contaminants such as per- and polyfluoroalkyl substances (PFAS) may impact surface-water quality and groundwater-dependent ecosystems of gaining streams. Although complex near-surface hydrogeology of stream corridors challenges sampling efforts, recent advances in heat tracing of discharge zones enable efficient and informed data collection. For this study, we used a combination of streambed temperature push-probe and thermal infrared methods to guide a discharge-zone-oriented sample collection along approximately 6 km of a coastal trout stream on Cape Cod, MA. Eight surface-water locations and discharging groundwater from 24 streambed and bank seepages were analysed for dissolved oxygen (DO), specific conductance, stable water isotopes, and a range of PFAS compounds, which are contaminants of emerging concern in aquatic environments. The results indicate a complex system of groundwater discharge source flowpaths, where the sum of concentrations of six PFAS compounds (corresponding to the U.S. Environmental Protection Agency third Unregulated Contaminant Monitoring Rule “UCMR 3”) showed a median concentration of 52 ± 331 (SD) ng/L with two higher outliers and three discharges with PFAS concentrations below the quantification limit. Higher PFAS concentration was related (− 0.66 Spearman rank, p < .001) to discharging groundwater that showed an evaporative signature (deuterium excess), indicating flow through at least one upgradient kettle lake. Therefore, more regional groundwater flowpaths originating from outside the local river corridor tended to show higher PFAS concentrations as evaluated at their respective discharge zones. Conversely, PFAS concentrations were typically low at discharges that did not indicate evaporation and were adjacent to steep hillslopes and, therefore, were classified as locally recharged groundwater. Previous research at this stream found that the native brook trout spawn at discharge points of groundwater recharged on local hillslopes, likely in response to generally higher levels of DO. Our study shows that by targeting high oxygen discharges the trout may thereby be avoiding emerging contaminants such as PFAS in groundwater recharged farther from the stream.  相似文献   

10.
Significant uncertainty remains in understanding the groundwater flow pathways in the northeastern Qinghai–Tibet Plateau. Hydrogeochemical and isotopic data as well as hydrogeological data were combined to explore the groundwater flow path in a representative cold alpine catchment in the headwater region of the Heihe River. The results indicate that the suprapermafrost groundwater chemical components were mainly affected by calcite dissolution and evaporation, whereas the geochemistry of subpermafrost groundwater was controlled by dolomite and gypsum dissolution, calcite precipitation, and albite and halite dissolution. Distinct hydrogeochemical characteristics and controlling processes suggest a poor hydraulic connectivity between the suprapermafrost and subpermafrost groundwater. The hydraulic connectivity between permafrost groundwater and groundwater in the seasonally frozen area was confirmed by their similar hydrogeochemical features. In the seasonally frozen area, a silty clay layer with low permeability separates the aquifer into the deep (depth >20 m) and shallow (depth <20 m) flow paths. The deep groundwater was characterized by the enhanced dedolomitization and enhanced cation exchange processes compared with the shallow groundwater. Groundwater in the seasonally frozen area finally discharges as base flow into the stream. These results provide useful information about the groundwater flow systems in the unique alpine gorge catchments in Qinghai–Tibet Plateau. The above findings suggest that the permafrost distribution and the aquifer structures within the seasonally frozen area have significant impact on groundwater flow paths. Cross‐validation by drilling work and hydrograph data confirms that the hydrogeochemical and isotopic tracers combined with field investigations can be relatively low‐cost tools in interpreting the groundwater flow paths in similar alpine catchments.  相似文献   

11.
Hydrochemical, inverse geochemical modelling and isotopic approaches are used to assess the hydrogeochemical evolution of groundwater from the basement aquifers in the southeastern part of the Plateaux Region, Togo. Groundwater originates from present-day rainwater infiltration and is mostly fresh and slightly acidic to neutral. Hydrochemical facies are predominantly mixed cations-HCO3 associated with Ca/Mg-Cl, Na-HCO3 and Na-Cl water types in equilibrium with kaolinite and Ca/Mg-smectites. They are related to silicates hydrolysis, anthropogenic contamination, nitrification/denitrification, mixing along flowpaths and dissolution/precipitation of secondary minerals. The pattern of flow paths is in accordance with an increasing trend in total dissolved solids (TDS) toward the potentiometric depression located in the central and southern parts of the aquifer system. Inverse geochemical modelling using the NETPATH-WIN model showed the relative importance of biotite, plagioclase and amphibole weathering and dissolution of secondary carbonate minerals along the flowpath, suggesting that an abundance of minerals is not necessarily the main factor controlling the groundwater chemistry evolution.  相似文献   

12.
Identifying the key factors controlling groundwater chemical evolution in mountain-plain transitional areas is crucial for the security of groundwater resources in both headwater basins and downstream plains. In this study, multivariate statistical techniques and geochemical modelling were used to analyse the groundwater chemical data from a typical headwater basin of the North China Plain. Groundwater samples were divided into three groups, which evolved from Group A with low mineralized Ca-HCO3 water, through Group B with moderate mineralized Ca-SO4-HCO3 water, to Group C with highly saline Ca-SO4 and Ca-Cl water. Water-rock interaction and nitrate contamination were mainly responsible for the variation in groundwater chemistry. Groundwater chemical compositions in Group A were mainly influenced by dissolution of carbonates and cation exchange, and suffered less nitrate contamination, closely relating to their locations in woodland and grassland with less pronounced human interference. Chemical evolution of groundwater in Groups B and C was gradually predominated by the dissolution of evaporites, reverse ion exchange, and anthropogenic factors. Additionally, the results of the inverse geochemical model showed that dedolomitization caused by gypsum dissolution, played a key role in the geochemical evolution from Group A to Group B. Heavy nitrate enrichment in most groundwater samples of Groups B and C was closely associated with the land-use patterns of farmland and residential areas. Apart from the high loads of chemical fertilizers in irrigation return flow as the main source for nitrate contamination, the stagnant zones, flood irrigation pattern, mine drainage, and groundwater-exploitation reduction program were also important contributors for such high mineralization and heavy NO3− contents in Group C. The important findings of this work not only provide the conceptual framework for the headwater basin but also have important implications for sustainable management of groundwater resources in other headwater basins of the North China Plain.  相似文献   

13.
ABSTRACT

A study of surface water chemistry evolution was conducted by multivariate statistical analysis and inverse geochemical modelling using the PHREEQC computer program. Using hierarchical cluster analysis the 14 sampling sites were classified into three groups (recharge, transition and discharge areas). Water chemistry changed along a flow path so that waters with Ca–HCO3 and Mg–Cl composition changed to Mg–Cl–HCO3 waters. The order of abundance of the major cations was Mg > Ca > Na > K. Their average concentrations were 21, 19, 3.6 and 2.5 mg L-1, respectively. Inverse geochemical modelling along flow paths indicated that the dissolution of sylvite and kaolinite, and precipitation of feldspars and andalusite, happened with Na entering the solution and Ca, Mg and K leaving the solution.
Editor D. Koutsoyiannis; Associate editor not assigned  相似文献   

14.
This study demonstrates the application of multivariate statistical methods in definition of groundwater recharge and discharge areas in a sedimentary basin in Ghana. Q‐mode hierarchical cluster analysis (HCA) was applied to 57 hydrochemical data from the Buem formation in the northern part of the Volta Region in Ghana. R‐mode HCA and R‐mode factor analysis were then applied to the same dataset to reveal the processes controlling the hydrochemistry of groundwater from this hydrogeological formation. Results of both the Q‐ and R‐mode analyses were backed by graphical methods. The analyses revealed two major water types, differentiated by salinity levels into four spatial groundwater associations. The characteristics of the four groundwater types are discussed. The recharge areas are characterized by Ca? HCO3 low salinity waters which evolve through rock–water interactions to Na? HCO3 high salinity waters in the discharge areas. This study finds that the hydrochemistry of groundwater from this formation is mainly controlled by the weathering of minerals, principally silicates in the aquifer matrix. The effects of the chemistry of recharging precipitation are higher in the recharge areas, while mineral weathering tends to be severe close to the discharge areas in the groundwater flow regime. All the four spatial groundwater associations have low sodium content, but salinity levels increase towards the discharge areas, such that some of wells in the discharge areas may not be acceptable for irrigation on grounds of high salinities which might affect the osmotic potentials of plants. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

15.
ABSTRACT

Multivariate statistical analysis and inverse geochemical modelling techniques were employed to deduce the mechanism of groundwater evolution in the hard-rock terrain of Telangana, South India. Q-mode hierarchical cluster analysis (HCA) and principal component analysis (PCA) were used to extract the hydrogeochemical characteristics and classify the groundwater samples into three principal groups. Use of thermodynamic stability diagrams and inverse geochemical modelling in PHREEQC identified the chemical reactions controlling hydrogeochemistry of each of the groups obtained from statistical analysis. The model output showed that a few phases are governing the water chemistry in this area and the geochemical reactions responsible for evolution of groundwater chemistry along the flow path are (i) dissolution of evaporite minerals (dolomite, halite); (ii) dissolution of primary silicate minerals (albite, anorthite, K-feldspar, biotite); (iii) precipitation of secondary silicate minerals (kaolinite, quartz, gibbsite, Ca-montmorillonite) along with anhydrite and calcite; and (iv) reverse ion exchange processes.  相似文献   

16.
The present work examines the possible use of major ion chemistry and multivariate statistical techniques as a rapid and relatively cost‐effective method of identifying the extent of groundwater and surface water (GW–SW) interaction in an urban setting. The original hydrogeochemical dataset consists of groundwater (n = 114), stream water (n = 42) and drain water (n = 24) samples, collected twice in a year for the pre‐ and post‐monsoon seasons, for three successive years along an 8 km reach of the Delhi segment of River Yamuna, India. The dynamic and similar seasonal changes of hydro‐geochemical facies and major ion trends of river, drain and groundwater samples indicate the existence of an empirical relationship between GW and SW. Results of both R‐ and Q‐mode factor and cluster analyses highlight multi‐scale control of the fluid exchange distributions, with distinct seasonal alteration in mode and extent of GW–SW interaction, namely, the influence of the mixing zones between urban river and groundwater and the pattern of groundwater flow through the river bed. Hierarchical cluster analysis (HCA) of sampling locations efficiently illustrates different groups that comprise samples severely influenced by contaminated surface water downstream and the upstream fresh water samples. These results substantiate the strong exchange processes between GW and SW all along the stretch. The study shows that the combination of an empirical and statistical relationship between different ionic species and sampling locations can provide greater confidence in identifying the extent of GW–SW interaction/exchange processes. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

17.
As Andean glaciers rapidly retreat due to climate change, the balance of groundwater and glacial meltwater contributions to stream discharge in tropical, proglacial watersheds will change, potentially increasing vulnerability of water resources. The Shullcas River Watershed, near Huancayo, Peru, is fed only partly by the rapidly receding Huaytapallana glaciers (<20% of dry season flow). To potentially increase recharge and therefore increase groundwater derived baseflow, the government and not‐for‐profit organizations have installed trenches along large swaths of hillslope in the Shullcas Watershed. Our study focuses on a nonglacierized subcatchment of the Shullcas River Watershed and has 2 objectives: (a) create a model of the Shullcas groundwater system and assess the controls on stream discharge and (b) investigate the impact of the infiltration trenches on recharge and baseflow. We first collected hydrologic data from the field including a year‐long hydrograph (2015–2016), meteorological data (2011–2016), and infiltration measurements. We use a recharge model to evaluate the impact of trenched hillslopes on infiltration and runoff processes. Finally, we use a 3‐dimensional groundwater model, calibrated to the measured dry season baseflow, to determine the impact of trenching on the catchment. Simulations show that trenched hillslopes receive approximately 3.5% more recharge, relative to precipitation, compared with unaltered hillslopes. The groundwater model indicates that because the groundwater flow system is fast and shallow, incorporating trenched hillslopes (~2% of study subcatchment area) only slightly increases baseflow in the dry season. Furthermore, the location of trenching is an important consideration: Trenching higher in the catchment (further from the river) and in flatter terrain provides more baseflow during the dry season. The results of this study may have important implications for Andean landscape management and water resources.  相似文献   

18.
It is often assumed that the net groundwater flow direction is towards the channel in headwater streams in humid climates, with magnitudes dependent on flow state. However, studies that characterize stream–groundwater interactions in ephemeral and intermittent streams in humid landscapes remain sparse. Here, we examined seasonally driven stream–groundwater interactions in response to temporary streamflow on the basis of field observations of streamflow and groundwater on an adjacent hillslope. The direction of hydraulic head gradients between the stream and groundwater shifted seasonally. The stream gained water (head gradients were towards the stream) when storage state was high. During this period, streamflow was persistent. The stream lost water to the groundwater system (head gradients were away from the stream) when storage state was low. During this period, streamflow only occurred in response to precipitation events, and head gradients remained predominantly away from the stream during events. This suggested that mechanisms other than deep groundwater contributions produced run‐off when storage was low, such as surface and perched subsurface flowpaths above the water table. Analysis of the annual water balance for the study period showed that the residual between precipitation inputs and streamflow and evapotranspiration outputs, which were attributed to the loss of water to the deeper, regional groundwater system, was similar in magnitude to streamflow. This, coupled with results that showed bidirectionality in stream–groundwater head gradients, indicated that headwaters composed of temporary (e.g., ephemeral and intermittent) streams can be important focal areas for regional groundwater recharge, and both contribute to and receive water, solutes, and materials from the groundwater system.  相似文献   

19.
Mineral weathering rates and a forest macronutrient uptake stoichiometry were determined for the forested, metabasaltic Hauver Branch watershed in north‐central Maryland, USA. Previous studies of Hauver Branch have had an insufficient number of analytes to permit determination of rates of all the minerals involved in chemical weathering, including biomass. More equations in the mass‐balance matrix were added using existing mineralogic information. The stoichiometry of a deciduous biomass term was determined using multi‐year weekly to biweekly stream‐water chemistry for a nearby watershed, which drains relatively unreactive quartzite bedrock. At Hauver Branch, calcite hosts ~38 mol% of the calcium ion (Ca2+) contained in weathering minerals, but its weathering provides ~90% of the stream water Ca2+. This occurs in a landscape with a regolith residence time of more than several Ka (kiloannum). Previous studies indicate that such old regolith does not typically contain dissolving calcite that affects stream Ca2+/Na+ ratios. The relatively high calcite dissolution rate likely reflects dissolution of calcite in fractures of the deep critical zone. Of the carbon dioxide (CO2) consumed by mineral weathering, calcite is responsible for approximately 27%, with the silicate weathering consumption rate far exceeding that of the global average. The chemical weathering of mafic terrains in decaying orogens thus may be capable of influencing global geochemical cycles, and therefore, climate, on geological timescales. Based on carbon‐balance calculations, atmospheric‐derived sulfuric acid is responsible for approximately 22% of the mineral weathering occurring in the watershed. Our results suggest that rising air temperatures, driven by global warming and resulting in higher precipitation, will cause the rate of chemical weathering in the Hauver Branch watershed to increase until a threshold temperature is reached. Beyond the threshold temperature, increased recharge would produce a shallower groundwater table and reduced chemical weathering rates. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

20.
Abstract

Groundwater of the Tertiary-Quaternary Formations in the Jeloula basin (Central Tunisia), together with rain and surface waters, were analysed to investigate the mineralization processes, the origin of the water and its recharge sources. The water samples present a large spatial variability of chemical facies which is related to their interaction with the geological formations. The main sources of the water mineralization are the dissolution of evaporitic and carbonate minerals and cation exchange reactions. Stable isotopes indicate that most groundwater samples originate from infiltration of modern precipitation. Surface water samples from small dam reservoirs show a 18O/2H enrichment, which is typical of water exposed to open-surface evaporation in a semi-arid region. Considerable data of 3H and 14C allow the qualitative identification of the present-day recharge that is probably supplied by infiltration of recent flood waters in the Wadi El Hamra valley, and by direct infiltration of meteoric water through the local carbonate outcrops.

Editor D. Koutsoyiannis; Associate editor S. Faye  相似文献   

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