Geochemical modelling baseline compositions of groundwater

DEFF Research Database (Denmark)

Postma, Diederik Jan; Kjøller, Claus; Andersen, Martin Søgaard

2008-01-01

and variations in water chemistry that are caused by large scale geochemical processes taking place at the timescale of thousands of years. The most important geochemical processes are ion exchange (Valreas and Aveiro) where freshwater solutes are displacing marine ions from the sediment surface, and carbonate......Reactive transport models, were developed to explore the evolution in groundwater chemistry along the flow path in three aquifers; the Triassic East Midland aquifer (UK), the Miocene aquifer at Valreas (F) and the Cretaceous aquifer near Aveiro (P). All three aquifers contain very old groundwaters...... dissolution (East Midlands, Valreas and Aveiro). Reactive transport models, employing the code PHREEQC, which included these geochemical processes and one-dimensional solute transport were able to duplicate the observed patterns in water quality. These models may provide a quantitative understanding...

Rock–water interactions and pollution processes in the volcanic aquifer system of Guadalajara, Mexico, using inverse geochemical modeling

International Nuclear Information System (INIS)

Morán-Ramírez, J.; Ledesma-Ruiz, R.; Mahlknecht, J.; Ramos-Leal, J.A.

2016-01-01

In order to understand and mitigate the deterioration of water quality in the aquifer system underlying Guadalajara metropolitan area, an investigation was performed developing geochemical evolution models for assessment of groundwater chemical processes. The models helped not only to conceptualize the groundwater geochemistry, but also to evaluate the relative influence of anthropogenic inputs and natural sources of salinity to the groundwater. Mixing processes, ion exchange, water–rock–water interactions and nitrate pollution and denitrification were identified and confirmed using mass-balance models constraint by information on hydrogeology, groundwater chemistry, lithology and stability of geochemical phases. The water–rock interactions in the volcanic setting produced a dominant Na−HCO_3 water type, followed by Na−Mg−Ca−HCO_3 and Na−Ca−HCO_3. For geochemical evolution modeling, flow sections were selected representing recharge and non-recharge processes and a variety of mixing conditions. Recharge processes are dominated by dissolution of soil CO_2 gas, calcite, gypsum, albite and biotite, and Ca/Na exchange. Non-recharge processes show that the production of carbonic acid and Ca/Na exchange are decreasing, while other minerals such as halite and amorphous SiO_2 are precipitated. The origin of nitrate pollution in groundwater are fertilizers in rural plots and wastewater and waste disposal in the urban area. This investigation may help water authorities to adequately address and manage groundwater contamination. - Highlights: • The Inverse geochemical modeling was used to study to processes occurring in a volcanic aquifer. • Three flow sections were selected to apply inverse hydrogeochemical modeling. • Three main groundwater flows were identified: a local, intermediate and regional flow. • The models show that in the study area that groundwater is mixed with local recharge. • In the south, the aquifer has thermal influence.

Potential environmental issues of CO2 storage in deep saline aquifers: Geochemical results from the Frio-I Brine Pilot test, Texas, USA

Science.gov (United States)

Kharaka, Yousif K.; Thordsen, James J.; Hovorka, Susan D.; Nance, H. Seay; Cole, David R.; Phelps, Tommy J.; Knauss, Kevin G.

2009-01-01

Sedimentary basins in general, and deep saline aquifers in particular, are being investigated as possible repositories for large volumes of anthropogenic CO2 that must be sequestered to mitigate global warming and related climate changes. To investigate the potential for the long-term storage of CO2 in such aquifers, 1600 t of CO2 were injected at 1500 m depth into a 24-m-thick "C" sandstone unit of the Frio Formation, a regional aquifer in the US Gulf Coast. Fluid samples obtained before CO2 injection from the injection well and an observation well 30 m updip showed a Na–Ca–Cl type brine with ∼93,000 mg/L TDS at saturation with CH4 at reservoir conditions; gas analyses showed that CH4 comprised ∼95% of dissolved gas, but CO2 was low at 0.3%. Following CO2 breakthrough, 51 h after injection, samples showed sharp drops in pH (6.5–5.7), pronounced increases in alkalinity (100–3000 mg/L as HCO3) and in Fe (30–1100 mg/L), a slug of very high DOC values, and significant shifts in the isotopic compositions of H2O, DIC, and CH4. These data, coupled with geochemical modeling, indicate corrosion of pipe and well casing as well as rapid dissolution of minerals, especially calcite and iron oxyhydroxides, both caused by lowered pH (initially ∼3.0 at subsurface conditions) of the brine in contact with supercritical CO2.These geochemical parameters, together with perfluorocarbon tracer gases (PFTs), were used to monitor migration of the injected CO2 into the overlying Frio “B”, composed of a 4-m-thick sandstone and separated from the “C” by ∼15 m of shale and siltstone beds. Results obtained from the Frio “B” 6 months after injection gave chemical and isotopic markers that show significant CO2 (2.9% compared with 0.3% CO2 in dissolved gas) migration into the “B” sandstone. Results of samples collected 15 months after injection, however, are ambiguous, and can be interpreted to show no additional injected CO2 in the “B” sandstone

Preliminary delineation of natural geochemical reactions, Snake River Plain aquifer system, Idaho National Engineering Laboratory and vicinity, Idaho

International Nuclear Information System (INIS)

Knobel, L.L.; Bartholomay, R.C.; Orr, B.R.

1997-05-01

The U.S. Geological Survey, in cooperation with the U.S. Department of Energy, is conducting a study to determine the natural geochemistry of the Snake River Plain aquifer system at the Idaho National Engineering Laboratory (INEL), Idaho. As part of this study, a group of geochemical reactions that partially control the natural chemistry of ground water at the INEL were identified. Mineralogy of the aquifer matrix was determined using X-ray diffraction and thin-section analysis and theoretical stabilities of the minerals were used to identify potential solid-phase reactants and products of the reactions. The reactants and products that have an important contribution to the natural geochemistry include labradorite, olivine, pyroxene, smectite, calcite, ferric oxyhydroxide, and several silica phases. To further identify the reactions, analyses of 22 representative water samples from sites tapping the Snake River Plain aquifer system were used to determine the thermodynamic condition of the ground water relative to the minerals in the framework of the aquifer system. Principal reactions modifying the natural geochemical system include congruent dissolution of olivine, diopside, amorphous silica, and anhydrite; incongruent dissolution of labradorite with calcium montmorillonite as a residual product; precipitation of calcite and ferric oxyhydroxide; and oxidation of ferrous iron to ferric iron. Cation exchange reactions retard the downward movement of heavy, multivalent waste constituents where infiltration ponds are used for waste disposal

Geochemical processes in a calcareous sandstone aquifer during managed aquifer recharge with desalinated seawater

Science.gov (United States)

Ganot, Yonatan; Russak, Amos; Siebner, Hagar; Bernstein, Anat; Katz, Yoram; Guttman, Jospeh; Kurtzman, Daniel

2017-04-01

In the last three years we monitor Managed Aquifer Recharge (MAR) of post-treated desalinated seawater (PTDES) in an infiltration pond, at the Menashe site that overlies the northern part of the Israeli Coastal Aquifer. The PTDES are stabilized with CaCO3 during post-treatment in the desalination plant and their chemical composition differs from those of any other water recharged to the aquifer and of the natural groundwater. We use suction cups in the unsaturated zone, shallow observation wells within the pond and production wells that encircles the MAR Menashe site, to study the geochemical processes during MAR with PTDES. Ion-enrichment (remineralization) of the recharged water was observed in both unsaturated zone and shallow observation wells samples. Enrichment occurs mainly in the first few meters below the pond surface by ion-exchange processes. Mg2+ enrichment is most prominent due to its deficiency in the PTDES. It is explained by ion-exchange with Ca2+, as the PTDES (enriched with Ca2+) infiltrates through a calcareous-sandstone aquifer with various amount of adsorbed Mg2+ (3-27 meq/kg). Hence, the higher concentration of Ca+2 in the PTDES together with its higher affinity to the sediments promotes the release of Mg2+ ions to the recharged water. Water isotopes analysis of the production wells were used to estimate residence time and mixing with local groundwater. At the end of 2016, it was found that the percentage of PTDES in adjacent down-gradient production wells was around 10%, while more distant or up-gradient wells show no mixing with PTDES. The distinct isotope contrast between the recharged desalinated seawater (δ2H=+11.2±0.2‰) and the local groundwater (δ2H ranged from -22.7 to -16.7‰) is a promising tool to evaluate future mixing processes at the Menshae MAR site. Using the Menashe MAR system for remineralization could be beneficial as a primary or complementary post-treatment technique. However, the sustainability of this process is

Behaviour and fate of nine recycled water trace organics during managed aquifer recharge in an aerobic aquifer

Science.gov (United States)

Patterson, B. M.; Shackleton, M.; Furness, A. J.; Bekele, E.; Pearce, J.; Linge, K. L.; Busetti, F.; Spadek, T.; Toze, S.

2011-03-01

The fate of nine trace organic compounds was evaluated during a 12 month large-scale laboratory column experiment. The columns were packed with aquifer sediment and evaluated under natural aerobic and artificial anaerobic geochemical conditions, to assess the potential for natural attenuation of these compounds during aquifer passage associated with managed aquifer recharge (MAR). The nine trace organic compounds were bisphenol A (BPA), 17β-estradiol (E2), 17α-ethynylestradiol (EE2), N-nitrosodimethylamine (NDMA), N-nitrosomorpholine (NMOR), carbamazepine, oxazepam, iohexol and iodipamide. In the low organic carbon content Spearwood sediment, all trace organics were non-retarded with retardation coefficients between 1.0 and 1.2, indicating that these compounds would travel at near groundwater velocities within the aquifer. The natural aerobic geochemical conditions provided a suitable environment for the rapid degradation for BPA, E2, iohexol (half life NDMA and NMOR) did not degrade under either aerobic or anaerobic aquifer geochemical conditions (half life > 50 days). Field-based validation experiments with carbamazepine and oxazepam also showed no degradation. If persistent trace organics are present in recycled waters at concentrations in excess of their intended use, natural attenuation during aquifer passage alone may not result in extracted water meeting regulatory requirements. Additional pre treatment of the recycled water would therefore be required.

Behaviour and fate of nine recycled water trace organics during managed aquifer recharge in an aerobic aquifer.

Science.gov (United States)

Patterson, B M; Shackleton, M; Furness, A J; Bekele, E; Pearce, J; Linge, K L; Busetti, F; Spadek, T; Toze, S

2011-03-25

The fate of nine trace organic compounds was evaluated during a 12month large-scale laboratory column experiment. The columns were packed with aquifer sediment and evaluated under natural aerobic and artificial anaerobic geochemical conditions, to assess the potential for natural attenuation of these compounds during aquifer passage associated with managed aquifer recharge (MAR). The nine trace organic compounds were bisphenol A (BPA), 17β-estradiol (E2), 17α-ethynylestradiol (EE2), N-nitrosodimethylamine (NDMA), N-nitrosomorpholine (NMOR), carbamazepine, oxazepam, iohexol and iodipamide. In the low organic carbon content Spearwood sediment, all trace organics were non-retarded with retardation coefficients between 1.0 and 1.2, indicating that these compounds would travel at near groundwater velocities within the aquifer. The natural aerobic geochemical conditions provided a suitable environment for the rapid degradation for BPA, E2, iohexol (half life aquifer geochemical conditions (half life >50days). Field-based validation experiments with carbamazepine and oxazepam also showed no degradation. If persistent trace organics are present in recycled waters at concentrations in excess of their intended use, natural attenuation during aquifer passage alone may not result in extracted water meeting regulatory requirements. Additional pre treatment of the recycled water would therefore be required. Crown Copyright © 2010. Published by Elsevier B.V. All rights reserved.

Contribution to the hydrogeological, geochemical and isotopic study of Ain El Beidha and Merguellil (Kairouan plain) aquifers: Implication for the dam-aquifer relationship

International Nuclear Information System (INIS)

Ben Ammar, Safouan

2007-01-01

In the semiarid central part of Tunisia the water resources are becoming increasingly rare because of the scarcity and irregularity of the precipitation and a steadily growing need for fresh water. This study addresses the use of geochemical and isotopic data to analyze the relationship between the El Haouareb dam and the Ain El Beidha and the Kairouan alluvial plain aquifers systems for durable groundwater management. In the Ain El Beidha basin the hydrogeological and geochemical investigations showed that: - The general direction of the groundwater flow is mainly from the SW to the NE, i.e. towards the hydraulic sill of El Haouareb which allows the connection between the Ain El Beidha basin and the Kairouan plain, - The salinity distribution displays a zonation in apparent relationship with the lithological variation of the aquifer formation, - Mineral exchange between groundwater and the aquifer matrix is the dominant process in determining groundwater salinity. The isotopic data confirm the flow directions of groundwater and shows that the recharge of Ain El Beidha aquifers takes place from the floods of the Khechem and Ben Zitoun wadies and also by preferential infiltration of runoff at the front of hill slopes area. Close to preferential recharge areas, groundwater 3H contents reflect a recent input of surface water, whereas the radiocarbon data indicate a longer residence time downstream. The isotopic characteristics of Ain El Beidha groundwater (small space and temporal changes) authorize the use of averaged values for the dam-aquifer water exchange. Under natural conditions, groundwater recharge of the alluvial aquifer of Kairouan plain occurs by infiltration of the Merguellil floods and from the Ain el Beidha groundwater flow close the karstic hydraulic sills. Since the construction of the El Haouareb dam, these natural mechanisms have been strongly modified: the dam waters infiltrate into the karst, mix with the Ain el Beidha groundwater, and feed the

Comparison of groundwater flow in Southern California coastal aquifers

Science.gov (United States)

Hanson, Randall T.; Izbicki, John A.; Reichard, Eric G.; Edwards, Brian D.; Land, Michael; Martin, Peter

2009-01-01

Development of the coastal aquifer systems of Southern California has resulted in overdraft, changes in streamflow, seawater intrusion, land subsidence, increased vertical flow between aquifers, and a redirection of regional flow toward pumping centers. These water-management challenges can be more effectively addressed by incorporating new understanding of the geologic, hydrologic, and geochemical setting of these aquifers.

Occurrence and geochemical behavior of arsenic in a coastal aquifer-aquitard system of the Pearl River Delta, China

Energy Technology Data Exchange (ETDEWEB)

Wang, Ya [Department of Earth Sciences, The University of Hong Kong, Hong Kong (China); Jiao, Jiu Jimmy, E-mail: jjiao@hku.hk [Department of Earth Sciences, The University of Hong Kong, Hong Kong (China); Cherry, John A. [School of Engineering, University of Guelph, Guelph, ON, Canada N1G 2W1 (Canada)

2012-06-15

Elevated concentrations of arsenic, up to 161 {mu}g/L, have been identified in groundwater samples from the confined basal aquifer underlying the aquitard of the Pearl River Delta (PRD). Both aquatic arsenic in pore water and solid arsenic in the sediments in the basal aquifer and aquitard were identified. Arsenic speciation of groundwater in the basal aquifer was elucidated on a pH-Eh diagram. In the PRD, arsenic is enriched in groundwater having both low and high salinity, and arsenic enriched groundwater is devoid of dissolved oxygen, has negative Eh values, is slightly alkaline, and has abnormally high concentrations of ammonium and dissolved organic carbon, but low concentrations of nitrate and nitrite. Results of geochemical and hydrochemical analyses and sequential extraction analysis suggest that reductive dissolution of iron oxyhydroxide could be one of the important processes that mobilized solid arsenic. We speculate that mineralization of sedimentary organic matter could also contribute to aquatic arsenic. Scanning electron microscope analysis confirms that abundant authigenic pyrite is present in the sediments. Sulphate derived from paleo-seawater served as the important sulfur source for authigenic pyrite formation. Co-precipitation of arsenic with authigenic pyrite significantly controlled concentrations of aquatic arsenic in the coastal aquifer-aquitard system. - Highlights: Black-Right-Pointing-Pointer Coastal aquifer and aquitard are treated as an integrate system. Black-Right-Pointing-Pointer Both aquatic arsenic and solid arsenic are observed. Black-Right-Pointing-Pointer Aquatic arsenic is derived from reductive dissolution of iron oxyhydroxide. Black-Right-Pointing-Pointer Aquatic arsenic can also derived from mineralization of sedimentary organic matter. Black-Right-Pointing-Pointer Co-precipitation of arsenic with authigenic pyrite is significant in such a system.

Geochemistry of the Arbuckle-Simpson Aquifer

Science.gov (United States)

Christenson, Scott; Hunt, Andrew G.; Parkhurst, David L.; Osborn, Noel I.

2009-01-01

The Arbuckle-Simpson aquifer in south-central Oklahoma provides water for public supply, farms, mining, wildlife conservation, recreation, and the scenic beauty of springs, streams, and waterfalls. A new understanding of the aquifer flow system was developed as part of the Arbuckle-Simpson Hydrology Study, done in 2003 through 2008 as a collaborative research project between the State of Oklahoma and the Federal government. The U.S. Geological Survey collected 36 water samples from 32 wells and springs in the Arbuckle-Simpson aquifer in 2004 through 2006 for geochemical analyses of major ions, trace elements, isotopes of oxygen and hydrogen, dissolved gases, and dating tracers. The geochemical analyses were used to characterize the water quality in the aquifer, to describe the origin and movement of ground water from recharge areas to discharge at wells and springs, and to determine the age of water in the aquifer.

Geochemical evolution of groundwater in carbonate aquifers of southern Latium region, central Italy

Directory of Open Access Journals (Sweden)

Giuseppe Sappa

2013-03-01

Full Text Available Spring and well water samples, from carbonate aquifers of Latium region, have been characterized to determine the hydrochemical processes governing the evolution of the groundwater. Most of the spring samples, issuing from Lepini, Ausoni and Aurunci Mts., are characterized as alkaline earth HCO3 waters, however, some samples show a composition of Cl--SO4 -- alkaline earth waters. Groundwater samples from Pontina Plain shows three different hydrochemical facies: alkaline earth HCO3 type, Cl-- SO4 -- alkaline earth type and Cl--SO4 -- alkaline type waters. Geochemical modeling and saturation index computation of the sampled waters show an interaction with calcareous and calcareous-dolomitic lithologies. Most of the springs and wells was kinetically saturated with respect to calcite and dolomite, and all the samples were below the equilibrium state with gypsum. This indicates that the groundwater has capacity to dissolve the gypsum along the flow paths. The electrical conductivity and Cl- concentrations of the sampled waters show a positive trend with the decrease in the distance from the coast, highlighting seawater intrusion in the coastal area. According to hydrochemistry results and geochemical modeling, the dominant factors in controlling the hydrochemical characteristics of groundwater are: (i water rock interaction with calcareous and calcareous-dolomitic lithologies; (ii seawater intrusion in the coastal area; (iii dissolution and/or precipitation of carbonate and (i.e. dolomite and calcite evaporate minerals (gypsum determined by saturation indexes; (iv mineral weathering process; (the high Mg/Ca ratio due to the weathering of Mg-rich dolomite.

Geochemical and flow modelling as tools in monitoring managed aquifer recharge

International Nuclear Information System (INIS)

Niinikoski, Paula; Saraperä, Sami; Hendriksson, Nina; Karhu, Juha A.

2016-01-01

Due to a growing world population and the effects of anthropogenic climate change, access to clean water is a growing global concern. Managed aquifer recharge (MAR) is a method that can help society's response to this increasing demand for pure water. In MAR, the groundwater resources are replenished and the quality of the recharged surface water is improved through effects such as the removal of organic matter. This removal occurs through mechanisms such as microbial decomposition, which can be monitored by studying the isotopic composition of dissolved inorganic carbon (DIC). Nevertheless, the monitoring can be difficult when there are other factors, like dissolving calcite, affecting the isotopic composition of DIC. The aims of this study were to establish a method for monitoring the decomposition of organic matter (dissolved organic carbon – DOC) in cases where calcite dissolution adds another component to the DIC pool, and to use this method to monitor the beginning and amount of DOC decomposition on a MAR site at Virttaankangas, southwestern Finland. To achieve this, we calculated the mean residence times of infiltrated water in the aquifer and the fractions of this water reaching observation wells. We conducted geochemical modelling, using PHREEQC, to estimate the amount of DOC decomposition and the mineral reactions affecting the quality of the water. - Highlights: • The decomposition of DOC in MAR systems is residence time dependent. • High pH environment can delay the beginning of the decomposition process. • Shortest travel times do not correlate with mean residence times in MAR systems.

Geochemical detection of carbon dioxide in dilute aquifers

Directory of Open Access Journals (Sweden)

Aines Roger

2009-03-01

Full Text Available Abstract Background Carbon storage in deep saline reservoirs has the potential to lower the amount of CO2 emitted to the atmosphere and to mitigate global warming. Leakage back to the atmosphere through abandoned wells and along faults would reduce the efficiency of carbon storage, possibly leading to health and ecological hazards at the ground surface, and possibly impacting water quality of near-surface dilute aquifers. We use static equilibrium and reactive transport simulations to test the hypothesis that perturbations in water chemistry associated with a CO2 gas leak into dilute groundwater are important measures for the potential release of CO2 to the atmosphere. Simulation parameters are constrained by groundwater chemistry, flow, and lithology from the High Plains aquifer. The High Plains aquifer is used to represent a typical sedimentary aquifer overlying a deep CO2 storage reservoir. Specifically, we address the relationships between CO2 flux, groundwater flow, detection time and distance. The CO2 flux ranges from 103 to 2 × 106 t/yr (0.63 to 1250 t/m2/yr to assess chemical perturbations resulting from relatively small leaks that may compromise long-term storage, water quality, and surface ecology, and larger leaks characteristic of short-term well failure. Results For the scenarios we studied, our simulations show pH and carbonate chemistry are good indicators for leakage of stored CO2 into an overlying aquifer because elevated CO2 yields a more acid pH than the ambient groundwater. CO2 leakage into a dilute groundwater creates a slightly acid plume that can be detected at some distance from the leak source due to groundwater flow and CO2 buoyancy. pH breakthrough curves demonstrate that CO2 leaks can be easily detected for CO2 flux ≥ 104 t/yr within a 15-month time period at a monitoring well screened within a permeable layer 500 m downstream from the vertical gas trace. At lower flux rates, the CO2 dissolves in the aqueous phase

Geochemistry of the Springfield Plateau aquifer of the Ozark Plateaus Province in Arkansas, Kansas, Missouri and Oklahoma, USA

Science.gov (United States)

Adamski, J.C.

2000-01-01

Geochemical data indicate that the Springfield Plateau aquifer, a carbonate aquifer of the Ozark Plateaus Province in central USA, has two distinct hydrochemical zones. Within each hydrochemical zone, water from springs is geochemically and isotopically different than water from wells. Geochemical data indicate that spring water generally interacts less with the surrounding rock and has a shorter residence time, probably as a result of flowing along discrete fractures and solution openings, than water from wells. Water type throughout most of the aquifer was calcium bicarbonate, indicating that carbonate-rock dissolution is the primary geochemical process occurring in the aquifer. Concentrations of calcium, bicarbonate, dissolved oxygen and tritium indicate that most ground water in the aquifer recharged rapidly and is relatively young (less than 40 years). In general, field-measured properties, concentrations of many chemical constituents, and calcite saturation indices were greater in samples from the northern part of the aquifer (hydrochemical zone A) than in samples from the southern part of the aquifer (hydrochemical zone B). Factors affecting differences in the geochemical composition of ground water between the two zones are difficult to identify, but could be related to differences in chert content and possibly primary porosity, solubility of the limestone, and amount and type of cementation between zone A than in zone B. In addition, specific conductance, pH, alkalinity, concentrations of many chemical constituents and calcite saturation indices were greater in samples from wells than in samples from springs in each hydrochemical zone. In contrast, concentrations of dissolved oxygen, nitrite plus nitrate, and chloride generally were greater in samples from springs than in samples from wells. Water from springs generally flows rapidly through large conduits with minimum water-rock interactions. Water from wells flow through small fractures, which restrict

Factors affecting public-supply well vulnerability in two karst aquifers.

Science.gov (United States)

Musgrove, MaryLynn; Katz, Brian G; Fahlquist, Lynne S; Crandall, Christy A; Lindgren, Richard J

2014-09-01

Karst aquifers occur in a range of climatic and geologic settings. Nonetheless, they are commonly characterized by their vulnerability to water-quality impairment. Two karst aquifers, the Edwards aquifer in south-central Texas and the Upper Floridan aquifer in western Florida, were investigated to assess factors that control the movement of contaminants to public-supply wells (PSWs). The geochemistry of samples from a selected PSW or wellfield in each aquifer was compared with that from nearby monitoring wells and regional PSWs. Geochemistry results were integrated with age tracers, flow modeling, and depth-dependent data to refine aquifer conceptual models and to identify factors that affect contaminant movement to PSWs. The oxic Edwards aquifer is vertically well mixed at the selected PSW/wellfield, although regionally the aquifer is geochemically variable downdip. The mostly anoxic Upper Floridan aquifer is affected by denitrification and also is geochemically variable with depth. In spite of considerable differences in geology and hydrogeology, the two aquifers are similarly vulnerable to anthropogenic contamination. Vulnerability in studied PSWs in both aquifers is strongly influenced by rapid karst flowpaths and the dominance of young (aquifers (nitrate, atrazine, deethylatrazine, tetrachloroethene, and chloroform). Specific consideration of water-quality protection efforts, well construction and placement, and aquifer response times to land-use changes and contaminant loading are discussed, with implications for karst groundwater management. © 2014 The Authors. Groundwater published by Wiley Periodicals, Inc. on behalf of National Ground Water Association.

Geochemical effects of CO2 sequestration in sandstones under simulated in situ conditions of deep saline aquifers

International Nuclear Information System (INIS)

Wigand, M.; Carey, J.W.; Schuett, H.; Spangenberg, E.; Erzinger, J.

2008-01-01

The geochemical effects of brine and supercritical CO 2 (SCCO 2 ) on reservoir rocks from deep (1500-2000 m) saline aquifers were examined via experimental simulation at in situ conditions. Dry sandstone samples were mounted in a triaxial cell and autoclave system, evacuated, and saturated with 1 M NaCl solution. The brine-rock system was allowed to react at 30 MPa confining pressure, 15 MPa pore fluid pressure, and 60 deg. C while SCCO 2 was injected at a pressure gradient of 1-2 MPa. The experiment was conducted for a period of 1496 h, during which fluids were periodically sampled and analyzed. The pH measured in partially degassed fluid samples at 25 deg. C decreased from a starting value of 7.0-4.3 (9 days) and finally 5.1 after saturation with SCCO 2 . Fluid analyses indicate that most of the major (e.g. Ca, Mg, Fe, Mn) and trace elements (e.g. Sr, Ba, Pb) of the sandstone increase in concentration during the reaction with brine and SCCO 2 . These results are supported by scanning electron microscopy which indicates dissolution of dolomite cement, K-feldspar, and albite. In addition to dissolution reactions the formation of montmorillonite was observed. By adjusting surface area and reaction rates of dissolution and precipitation, geochemical modeling of the experiments could reproduce long-term trends in solution chemistry and indicated limited rates of dissolution as the system remained strongly undersaturated with most minerals, including carbonates. The geochemical models could not account for decreases in concentration of some elements, changes in solution composition resulting from changes in imposed pressure gradient, and the observed Ca/Mg and Si/Al ratios in solution

Geochemical detection of carbon dioxide in dilute aquifers.

Science.gov (United States)

Carroll, Susan; Hao, Yue; Aines, Roger

2009-03-26

Carbon storage in deep saline reservoirs has the potential to lower the amount of CO2 emitted to the atmosphere and to mitigate global warming. Leakage back to the atmosphere through abandoned wells and along faults would reduce the efficiency of carbon storage, possibly leading to health and ecological hazards at the ground surface, and possibly impacting water quality of near-surface dilute aquifers. We use static equilibrium and reactive transport simulations to test the hypothesis that perturbations in water chemistry associated with a CO2 gas leak into dilute groundwater are important measures for the potential release of CO2 to the atmosphere. Simulation parameters are constrained by groundwater chemistry, flow, and lithology from the High Plains aquifer. The High Plains aquifer is used to represent a typical sedimentary aquifer overlying a deep CO2 storage reservoir. Specifically, we address the relationships between CO2 flux, groundwater flow, detection time and distance. The CO2 flux ranges from 10(3) to 2 x 10(6) t/yr (0.63 to 1250 t/m2/yr) to assess chemical perturbations resulting from relatively small leaks that may compromise long-term storage, water quality, and surface ecology, and larger leaks characteristic of short-term well failure. For the scenarios we studied, our simulations show pH and carbonate chemistry are good indicators for leakage of stored CO2 into an overlying aquifer because elevated CO2 yields a more acid pH than the ambient groundwater. CO2 leakage into a dilute groundwater creates a slightly acid plume that can be detected at some distance from the leak source due to groundwater flow and CO2 buoyancy. pH breakthrough curves demonstrate that CO2 leaks can be easily detected for CO2 flux >or= 10(4) t/yr within a 15-month time period at a monitoring well screened within a permeable layer 500 m downstream from the vertical gas trace. At lower flux rates, the CO2 dissolves in the aqueous phase in the lower most permeable unit and does

Seasonal Hydrologic Controls on Uranium and Iron Biogeochemistry in a Riparian Aquifer

Science.gov (United States)

Wilkins, M.; Williams, K. H.; Danczak, R. E.; Yabusaki, S.; Fang, Y.; Hobson, C.

2015-12-01

The maintenance of geochemically reducing conditions is generally optimal for the formation and preservation of reduced metals and mineral phases that can limit contaminant fate and transport. At a riparian aquifer near Rifle, CO, we tracked over six months the biogeochemical response within the aquifer to an annual pulse of dissolved oxygen (DO) that results from snowmelt-driven changes in Colorado River stage. In reduced portions of the aquifer (naturally reduced zones; NRZs) the re-oxidation of abundant iron sulfide minerals was the dominant oxygen-consuming process, and resulted in little DO intrusion into the deeper aquifer. In less reduced areas, DO intruded through the entire vertical profile of the aquifer. Across both regions, these perturbations resulted in changes to the microbial community structure, and aqueous metal pools. Two potentially different mechanisms of uranium mobilization were observed; (1) re-oxidation of reduced U(IV) phases in response to DO intrusion, and (2) mobilization of U(VI) from the vadose zone during water table rise. This high-resolution, long-term monitoring of aquifer biogeochemistry at the Rifle site has revealed dynamic microbial and geochemical responses to predictable, annual hydrologic perturbations, and offers an opportunity to further refine modeling approaches for such regions.

Ground-water-quality assessment of the Central Oklahoma Aquifer, Oklahoma: geochemical and geohydrologic investigations

Science.gov (United States)

Parkhurst, David L.; Christenson, Scott C.; Breit, George N.

1993-01-01

The National Water-Quality Assessment pilot project for the Central Oklahoma aquifer examined the chemical and isotopic composition of ground water, the abundances and textures of minerals in core samples, and water levels and hydraulic properties in the flow system to identify geochemical reactions occurring in the aquifer and rates and directions of ground-water flow. The aquifer underlies 3,000 square miles of central Oklahoma and consists of Permian red beds, including parts of the Permian Garber Sandstone, Wellington Formation, and Chase, Council Grove, and Admire Groups, and Quaternary alluvium and terrace deposits.In the part of the Garber Sandstone and Wellington Formation that is not confined by the Permian Hennessey Group, calcium, magnesium, and bicarbonate are the dominant ions in ground water; in the confined part of the Garber Sandstone and Wellington Formation and in the Chase, Council Grove, and Admire Groups, sodium and bicarbonate are the dominant ions in ground water. Nearly all of the Central Oklahoma aquifer has an oxic or post-oxic environment as indicated by the large dissolved concentrations of oxygen, nitrate, arsenic(V), chromium(VI), selenium(VI), vanadium, and uranium. Sulfidic and methanic environments are virtually absent.Petrographic textures indicate dolomite, calcite, sodic plagioclase, potassium feldspars, chlorite, rock fragments, and micas are dissolving, and iron oxides, manganese oxides, kaolinite, and quartz are precipitating. Variations in the quantity of exchangeable sodium in clays indicate that cation exchange is occurring within the aquifer. Gypsum may dissolve locally within the aquifer, as indicated by ground water with large concentra-tions of sulfate, but gypsum was not observed in core samples. Rainwater is not a major source for most elements in ground water, but evapotranspiration could cause rainwater to be a significant source of potassium, sulfate, phosphate and nitrogen species. Brines derived from seawater are

Geochemical evolution of groundwater in the Mud Lake area, eastern Idaho, USA

Science.gov (United States)

Rattray, Gordon W.

2015-01-01

Groundwater with elevated dissolved-solids concentrations—containing large concentrations of chloride, sodium, sulfate, and calcium—is present in the Mud Lake area of Eastern Idaho. The source of these solutes is unknown; however, an understanding of the geochemical sources and processes controlling their presence in groundwater in the Mud Lake area is needed to better understand the geochemical sources and processes controlling the water quality of groundwater at the Idaho National Laboratory. The geochemical sources and processes controlling the water quality of groundwater in the Mud Lake area were determined by investigating the geology, hydrology, land use, and groundwater geochemistry in the Mud Lake area, proposing sources for solutes, and testing the proposed sources through geochemical modeling with PHREEQC. Modeling indicated that sources of water to the eastern Snake River Plain aquifer were groundwater from the Beaverhead Mountains and the Camas Creek drainage basin; surface water from Medicine Lodge and Camas Creeks, Mud Lake, and irrigation water; and upward flow of geothermal water from beneath the aquifer. Mixing of groundwater with surface water or other groundwater occurred throughout the aquifer. Carbonate reactions, silicate weathering, and dissolution of evaporite minerals and fertilizer explain most of the changes in chemistry in the aquifer. Redox reactions, cation exchange, and evaporation were locally important. The source of large concentrations of chloride, sodium, sulfate, and calcium was evaporite deposits in the unsaturated zone associated with Pleistocene Lake Terreton. Large amounts of chloride, sodium, sulfate, and calcium are added to groundwater from irrigation water infiltrating through lake bed sediments containing evaporite deposits and the resultant dissolution of gypsum, halite, sylvite, and bischofite.

Isotopic and geochemical evidence of recharge sources and water quality in the Quaternary aquifer beneath Jinchang city, NW China

International Nuclear Information System (INIS)

Ma Jinzhu; Pan Feng; Chen Lihua; Edmunds, W. Mike; Ding Zhenyu; He Jianhua; Zhou Kunpeng; Huang Tianming

2010-01-01

Multiple isotopic and hydrogeochemical tracers were utilized to understand the recharge sources and geochemical evolution of groundwater in the Quaternary aquifer beneath Jinchang city and the adjacent Gobi desert area. The groundwater shows markedly depleted stable isotopic composition compared to modern rainfall. The signature of groundwaters from Jinchang and the northern Gobi desert area differ clearly from that of the alluvial fan in the south Yongchang basin and modern rainfall, and has lower or non-detectable 3 H activity, implying that the aquifer is likely maintained by palaeowater. This groundwater in the Gobi desert has a 14 C age older than 12 ka, indicating that the groundwater resources are non-renewable. The build-up of dissolved solids through evaporation is a major control on groundwater composition, and the dominant anion species change systematically from HCO 3 - , SO 4 2- to Cl - , but cations from weathering of albite, calcite, dolomite and gypsum also make a significant contribution. The scientific results have important implications for groundwater management in Jinchang city and as well as in the Shiyang River basin under China's West Development Strategy. It is recommended that the water allocation program of diverting water from the Dongda river to the Minqin basin be reconsidered.

Geochemical and isotopic study to determine sources and processes affecting nitrate and sulphate in groundwater influenced by intensive human activity - carbonate aquifer Gliwice (southern Poland)

International Nuclear Information System (INIS)

Jakóbczyk-Karpierz, Sabina; Sitek, Sławomir; Jakobsen, Rasmus; Kowalczyk, Andrzej

2017-01-01

A multi-species, multi-stable-isotope approach (δ"1"5N_N_O_3, δ"1"8O_N_O_3_, δ"3"4S_S_O_4, δ"1"8O_S_O_4, δ"1"8O_H_2_O and δ"2H_H_2_O) was used together with environmental tracers (Ar, Ne, CFC-11 and CFC-12) and geochemical modelling to characterize sources and processes controlling concentrations of NO_3"− and SO_4"2"- in groundwater of the carbonate aquifer Gliwice (southern Poland). The study area represents a strongly transformed environment with a range of human activities i.a. Agriculture, urbanization and industry. The δ"1"5N_N_O_3 and δ"1"8O_N_O_3 indicated that most samples contained NO_3"− of mixed sources: artificial fertilizers, municipal and industrial sewage, while very good correlation between NO_3"− and CFC-12 suggested that nitrate originated primarily from residential and industrial sewage. Conversely, isotopic composition of sulphate in groundwater suggested agriculture as well as oxidation of sulphides as dominant. The conclusion was supported by the comparison of CFCs and sulphate concentrations which revealed no relevant correlation. Geochemical modelling confirmed the presence of sulphate reduction in areas where isotopic analyses were not possible due to undetectable sulphate. Thus, the integrated application of stable isotopes, environmental tracers, groundwater chemistry and geochemical modelling shows a complex origin of groundwater pollution in the study area as well as variety of geochemical processes controlling chemistry of groundwater in a triple-porosity aquifer influenced by different types of human activity. - Highlights: • CFCs helped to identify municipal and industrial sources of NO_3"− in groundwater. • δ"1"8O and δ"3"4S suggested domination of SO_4"2"- from agriculture and sulphide oxidation. • Sulphate reduction was confirmed using geochemical modelling for SO_4"2"-free water.

Geochemical evidence of groundwater flow paths and the fate and transport of constituents of concern in the alluvial aquifer at Fort Wingate Depot Activity, New Mexico, 2009

Science.gov (United States)

Robertson, Andrew J.; Henry, David W.; Langman, Jeffery B.

2013-01-01

accidental spill of perchlorate was spatially limited, and that dilution is the primary attenuation process for these constituents. The explosive concentrations of the nitramine 1,3,5-trinitroperhydro-1,3,5-triazine (RDX) and the oxidizer perchlorate both support that determination. Unlike RDX and perchlorate, there were no detectable concentrations of trinitrotoluene (TNT) in the aquifer. Based on the chemical nature of TNT and the redox conditions found in the aquifer, it is interpreted that TNT is lost to irreversible sorption and aerobic degradation. Nitrate was ubiquitous in the alluvial groundwater in October 2009. The nitrate concentrations in wells associated with the explosives’ groundwater flow path indicate attenuation primarily through dilution, similar to that of RDX. The origin of nitrate concentrations in the wells located in the Administration Area is uncertain but may have resulted from the leakage of aging clay sewage pipes that service most of the structures within that area or as a relic of a former hydrologic regime in which water from the washout operation migrated across a broader area. Sufficient data do not exist to definitively identify the location(s) of water discharge in this area, but transpiration from near the Administration Area is supported by the geochemical concentrations.

Searching for an Acidic Aquifer in the Rio Tinto Basin: First Geobiology Results of MARTE Project

Science.gov (United States)

Fernandez-Remolar, D. C.; Prieto-Ballesteros, O.; Stoker, C.

2004-01-01

Among the conceivable modern habitats to be explored for searching life on Mars are those potentially developed underground. Subsurface habitats are currently environments that, under certain physicochemical circumstances, have high thermal and hydrochemical stability [1, 2]. In planets like Mars lacking an atmospheric shield, such systems are obviously protected against radiation, which strongly alters the structure of biological macromolecules. Low porosity but fractured aquifers currently emplaced inside ancient volcano/sedimentary and hydrothermal systems act as excellent habitats [3] due to its thermal and geochemical properties. In these aquifers the temperature is controlled by a thermal balance between conduction and advection processes, which are driven by the rock composition, geological structure, water turnover of aquifers and heat generation from geothermal processes or chemical reactions [4]. Moreover, microbial communities based on chemolithotrophy can obtain energy by the oxidation of metallic ores that are currently associated to these environments. Such a community core may sustain a trophic web composed of non-autotrophic forms like heterotrophic bacteria, fungi and protozoa.

Modelling of Pesticide Transport During An Injection Experiment In A Physical and Geochemical Heterogeneous Aquifer

Science.gov (United States)

Hojberg, A. L.; Engesgaard, P.; Bjerg, P. L.

The fate of selected pesticides under natural groundwater conditions was studied by natural gradient short and long term injection experiments in a shallow uncon- fined aerobic aquifer. Bentazone, DNOC, MCPP, dichlorprop, isoproturon, and BAM (dichlobenil metabolite) were injected in aqueous solution with bromide as a nonre- active tracer. The Bromide and pesticide plumes were sampled during the initial 25 m of migration in a dense monitoring net of multilevel samplers. The aquifer was physical and geochemical heterogeneous, which affected transport of several of the pesticides. A 3D reactive transport code was developed including one- and two-site linear/nonlinear equilibrium/nonequilibrium sorption and first-order as well as single Monod degradation kinetic coupled to microbial growth. Model simulations demon- strated that microbial growth was likely supported by the phenoxy acids MCPP and dichlorprop, while degradation of DNOC was adequately described by first-order degradation with no initial lag time. An observed vertical increase in pH was observed at the site and implemented in the transport code. The numerical analysis indicated that degradation of the three degradable pesticides may have been affected by vertical pH variations. Spatial variability in observed DNOC sorption was similarly suspected to be an effect of varying pH. pH dependency on DNOC sorption was confirmed by the model recognized by a match to observed breakthrough at the individual sampling points, when pH variation was included in the simulations.

Hydrological and geochemical consequences of river regulation - hyporheic perspective

Science.gov (United States)

Siergieiev, Dmytro; Lundberg, Angela; Widerlund, Anders

2014-05-01

River-aquifer interfaces, essential for ecosystem functioning in terms of nutrient exchange and biological habitat, appear greatly threatened worldwide. Although river regulation is a vast pressure on river-aquifer interaction, influencing entire watersheds, knowledge about hyporheic exchange in regulated rivers is rather limited. In this study, we combine two decades of research on hydrological and geochemical impacts of hydropower regulation on river water and hyporheic zone in two large boreal rivers, unregulated Kalix River and regulated Lule River. Altered river discharge, with reduced spring peaks, daily summer fluctuations and elevated winter base flow severely modified Lule River water geochemistry and thus the transport of solutes to the Bothnian Bay (Baltic Sea). Further, these river modifications changed the river-aquifer exchange on both daily and seasonal scale, which resulted in deteriorated hyporheic conditions with reduced riverbed hydraulic conductivity (formation of a clogging layer) reflected in a declined hyporheic flux. Altered hydrological regime of the hyporheic zone created quasi-stagnant conditions beneath the river-aquifer interface and promoted the formation of geochemically suboxic environment. Taken that hyporheic water is a mixture of river water and groundwater, mixing models for the regulated site demonstrate a considerable addition of Fe, Mn, Al, NH4 and removal of dissolved oxygen and nitrate, which suggests the hyporheic zone in the Lule River to be a source of solutes. This contradicts the observations from the hyporheic zone in the unregulated river, with opposite behaviour functioning as a barrier. These results suggest that the hyporheic zone function is dependent on the river discharge and the state of the river-aquifer connectivity. Improved knowledge about the latter on a watershed scale will substantially increase our understanding about the status and potential pressures of riverine ecosystems and assist management and

Laboratory investigations into the reactive transport module of carbon dioxide sequestration and geochemical simulation

Energy Technology Data Exchange (ETDEWEB)

Heidaryan, E. [Islamic Azad Univ., Tehran (Iran, Islamic Republic of). Masjidosolayman Branch; Enayati, M.; Mokhtari, B. [Iranian Offshore Oil Co., Tehran (Iran, Islamic Republic of)

2008-07-01

Over long time periods, geological sequestration in some systems shows mineralization effects or mineral sequestration of carbon dioxide, converting the carbon dioxide to a less mobile form. However, a detailed investigation of these geological systems is needed before disposing of carbon dioxide into these formations. Depleted oil and gas reservoirs and underground aquifers are proposed candidates for carbon dioxide injection. This paper presented an experimental investigation into the reactive transport module for handling aquifer sequestration of carbon dioxide and modeling of simultaneous geochemical reactions. Two cases of laboratory carbon dioxide sequestration experiments, conducted for different rock systems were modeled using the fully coupled geochemical compositional simulator. The relevant permeability relationships were compared to determine the best fit with the experimental results. The paper discussed the theory of modeling; geochemical reactions and mineral trapping of carbon dioxide; and application simulator for modeling including the remodeling of flow experiments. It was concluded that simulated changes in porosity and permeability could mimic experimental results to some extent. The study satisfactorily simulated the results of experimental observations and permeability results could be improved if the Kozeny-Carman equation was replaced by the Civan power law. 6 refs., 2 tabs., 21 figs.

Land-use change and managed aquifer recharge effects on the hydrogeochemistry of two contrasting atoll island aquifers, Roi-Namur Island, Republic of the Marshall Islands

Science.gov (United States)

Hejazian, Mehrdad; Gurdak, Jason J.; Swarzenski, Peter W.; Odigie, Kingsley; Storlazzi, Curt

2017-01-01

Freshwater resources on low-lying atoll islands are highly vulnerable to climate change and sea-level rise. In addition to rainwater catchment, groundwater in the freshwater lens is a critically important water resource on many atoll islands, especially during drought. Although many atolls have high annual rainfall rates, dense natural vegetation and high evapotranspiration rates can limit recharge to the freshwater lens. Here we evaluate the effects of land-use/land-cover change and managed aquifer recharge on the hydrogeochemistry and supply of groundwater on Roi-Namur Island, Republic of the Marshall Islands. Roi-Namur is an artificially conjoined island that has similar hydrogeology on the Roi and Namur lobes, but has contrasting land-use/land-cover and managed aquifer recharge only on Roi. Vegetation removal and managed aquifer recharge operations have resulted in an estimated 8.6 x 105 m3 of potable groundwater in the freshwater lens on Roi, compared to only 1.6 x 104 m3 on Namur. We use groundwater samples from a suite of 33 vertically nested monitoring wells, statistical testing, and geochemical modeling using PHREEQC to show that the differences in land-use/land-cover and managed aquifer recharge on Roi and Namur have a statistically significant effect on several groundwater-quality parameters and the controlling geochemical processes. Results also indicate a seven-fold reduction in the dissolution of carbonate rock in the freshwater lens and overlying vadose zone of Roi compared to Namur. Mixing of seawater and the freshwater lens is a more dominant hydrogeochemical process on Roi because of the greater recharge and flushing of the aquifer with freshwater as compared to Namur. In contrast, equilibrium processes and dissolution-precipitation non-equilibrium reactions are more dominant on Namur because of the longer residence times relative to the rate of geochemical reactions. Findings from Roi-Namur Island support selective land-use/land-cover change and

Geochemical evidence for groundwater behavior in an unconfined aquifer, south Florida

Science.gov (United States)

Meyers, Jayson B.; Swart, Peter K.; Meyers', Janet L.

1993-07-01

Five well sites have been investigated along an east-west transect across the surfical aquifer system (SAS) of south Florida. Differences between rainfall during wet seasons (June-October) and evaporation during dry seasons (November-May) give surface waters of this region isotopically light ( δ 18O -22‰ and δ D -7.6‰ ) and heavy ( δ 18O +4.2‰ ) compositions, respectively. Surface waters and shallow groundwaters are enriched in 18O and D to the west, which is consistent with westward decrease in equal excess of rainfall. In the shallow portion of the SAS (less than 20 m, Biscayne sub-aquifer) heterogeneous stable isotopic compositions occur over short spans of time (less than 90 days), reflecting seasonal changes in the isotopic composition of recharge and rapid flushing. Homogeneous stable isotopic compositions occur below the Biscayne sub-aquifer, marking the zone of delayed circulation. Surface evaporation calculated from a stable isotope evaporation model agrees with previously published estimates of 75-95% by physical evaporation measurements and water budget calculations. This model contains many parameters that are assumed to be mean values, but short-term variability in some of these parameters may make this model unsuitable for the application of yearly mean values. For the Everglades, changes in the isotopic composition of atmospheric vapor during the dry season may cause the model to yield anomalous results when annual mean values are used. Chloride-enriched waters (more than 280 mg 1 -1) form a plume emanating from the bottom central portion of the transect. Elevated chloride concentration and light stable isotopic composition ( δ 18O ≈ -2‰ , δ D ≈ -8‰ ) suggest this plume is probably caused not by salinity of residual seawater in the aquifer, but by leakage from the minor artesian water-bearing zone of the Floridan aquifer system. Stable isotope values from Floridan aquifer groundwater plot close to the meteoric water line, in the

Spatial and temporal changes in sulphate-reducing groundwater bacterial community structure in response to Managed Aquifer Recharge.

Science.gov (United States)

Reed, D A; Toze, S; Chang, B

2008-01-01

The population dynamics of bacterial able to be cultured under sulphate reducing condition was studied in conjunction with changes in aquifer geochemistry using multivariate statistics for two contrasting Managed Aquifer Recharge (MAR) techniques at two different geographical locations (Perth, Western Australia and Adelaide, South Australia). Principal component analysis (PCA) was used to investigate spatial and temporal changes in the overall chemical signature of the aquifers using an array of chemical analytes which demonstrated a migrating geochemical plume. Denaturing Gradient Gel Electrophoresis (DGGE) using DNA from sulphate-reducing bacteria cultures was used to detect spatial and temporal changes in population dynamics. Bacterial and geochemical evidence suggested that groundwater at greatest distance from the nutrient source was least affected by treated effluent recharge. The results suggested that bacterial populations that were able to be cultured in sulphate reducing media responded to the migrating chemical gradient and to the changes in aquifer geochemistry. Most noticeably, sulphate-reducing bacterial populations associated with the infiltration galleries were stable in community structure over time. Additionally, the biodiversity of these culturable bacteria was restored when aquifer geochemistry returned to ambient conditions during the recovery phase at the Adelaide Aquifer Storage and Recovery site. Copyright CSIRO 2008.

Identifying and quantifying geochemical and mixing processes in the Matanza-Riachuelo Aquifer System, Argentina.

Science.gov (United States)

Armengol, S; Manzano, M; Bea, S A; Martínez, S

2017-12-01

The Matanza-Riachuelo River Basin, in the Northeast of the Buenos Aires Province, is one of the most industrialized and populated region in Argentina and it is worldwide known for its alarming environmental degradation. In order to prevent further damages, the aquifer system, which consists of two overlaid aquifers, is being monitored from 2008 by the river basin authority, Autoridad de la Cuenca Matanza-Riachuelo. The groundwater chemical baseline has been established in a previous paper (Zabala et al., 2016), and this one is devoted to the identification of the main physical and hydrogeochemical processes that control groundwater chemistry and its areal distribution. Thirty five representative groundwater samples from the Upper Aquifer and thirty four from the deep Puelche Aquifer have been studied with a multi-tool approach to understand the origin of their chemical and isotopic values. The resulting conceptual model has been validated though hydrogeochemical modeling. Most of the aquifer system has fresh groundwater, but some areas have brackish and salt groundwater. Water recharging the Upper Aquifer is of the Ca-HCO 3 type as a result of soil CO 2 and carbonate dissolution. Evapotranspiration plays a great role concentrating recharge water. After recharge, groundwater becomes Na-HCO 3 , mostly due to cation exchange with Na release and Ca uptake, which induces calcite dissolution. Saline groundwaters exist in the lower and upper sectors of the basin as a result of Na-HCO 3 water mixing with marine water of different origins. In the upper reaches, besides mixing with connate sea water other sources of SO 4 exist, most probably gypsum and/or sulfides. This work highlights the relevance of performing detailed studies to understand the processes controlling groundwater chemistry at regional scale. Moreover, it is a step forward in the knowledge of the aquifer system, and provides a sound scientific basis to design effective management programs and recovery plans

Experimental and modeling results on geochemical impacts of leaking CO2 from subsurface storage reservoirs to an unconfined oxidizing carbonate aquifer

Science.gov (United States)

Qafoku, N. P.; Bacon, D. H.; Shao, H.; Lawter, A.; Wang, G.; Brown, C. F.

2013-12-01

Deep subsurface storage and sequestration of CO2 has been identified as a potential mitigation technique for rising atmospheric CO2 concentrations. Sequestered CO2 represents a potential risk to overlying aquifers if the CO2 leaks from the deep storage reservoir. Experimental and modeling work is required to evaluate risks to groundwater quality and develop a systematic understanding on how CO2 leakage may cause important changes in aquifer chemistry and mineralogy by promoting dissolution/precipitation, adsorption/desorption, and redox reactions. Solid materials (rocks and slightly weathered rocks) from an unconfined aquifer, i.e., the Edwards Aquifer in Texas, were used in this investigation. The experimental part consisted of: 1) wet chemical acid extractions (8M HNO3 solution at 90 0C); 2) batch experiments conducted at low solid to solution ratios to study time-dependent releases of major, minor and trace elements during periodic or continuous exposure to CO2 gas; 3) hydraulically saturated column experiments conducted under continuous and stop-flow conditions using a CO2 gas saturated synthetic groundwater; 4) pre- and post-treatment solid phase characterization studies. Major variables tested included reaction time (0-336 hours), CO2 flow rate (50 to 350 ml/min), brine concentration (0.1 and 1 M NaCl), rock type and particle size fraction. We are currently investigating the solution composition effects (i.e., presence of contaminants in the initial solution) on the fate and behavior of potential contaminants (As, Pb and Cd) in these systems. Results from the solid phase characterization studies showed that the mineralogy of the Edwards aquifer materials was dominated by calcite. Quartz and montmorillonite were also present in some samples. Acid extractions confirmed that the solid phase had appreciable amounts of potential contaminants (As, Cd, Cr, Cu, Pb and Zn). However, the results from the batch and column experiments demonstrated that these contaminants

Experimental investigation of geochemical and mineralogical effects of CO2 sequestration on flow characteristics of reservoir rock in deep saline aquifers

Science.gov (United States)

Rathnaweera, T. D.; Ranjith, P. G.; Perera, M. S. A.

2016-01-01

Interactions between injected CO2, brine, and rock during CO2 sequestration in deep saline aquifers alter their natural hydro-mechanical properties, affecting the safety, and efficiency of the sequestration process. This study aims to identify such interaction-induced mineralogical changes in aquifers, and in particular their impact on the reservoir rock’s flow characteristics. Sandstone samples were first exposed for 1.5 years to a mixture of brine and super-critical CO2 (scCO2), then tested to determine their altered geochemical and mineralogical properties. Changes caused uniquely by CO2 were identified by comparison with samples exposed over a similar period to either plain brine or brine saturated with N2. The results show that long-term reaction with CO2 causes a significant pH drop in the saline pore fluid, clearly due to carbonic acid (as dissolved CO2) in the brine. Free H+ ions released into the pore fluid alter the mineralogical structure of the rock formation, through the dissolution of minerals such as calcite, siderite, barite, and quartz. Long-term CO2 injection also creates a significant CO2 drying-out effect and crystals of salt (NaCl) precipitate in the system, further changing the pore structure. Such mineralogical alterations significantly affect the saline aquifer’s permeability, with important practical consequences for the sequestration process. PMID:26785912

Modeling carbon dioxide sequestration in saline aquifers: Significance of elevated pressures and salinities

International Nuclear Information System (INIS)

Allen, D.E.; Strazisar, B.R.; Soong, Y.; Hedges, S.W.

2005-01-01

The ultimate capacity of saline formations to sequester carbon dioxide by solubility and mineral trapping must be determined by simulating sequestration with geochemical models. These models, however, are only as reliable as the data and reaction scheme on which they are based. Several models have been used to make estimates of carbon dioxide solubility and mineral formation as a function of pressure and fluid composition. Intercomparison of modeling results indicates that failure to adjust all equilibrium constants to account for elevated carbon dioxide pressures results in significant errors in both solubility and mineral formation estimates. Absence of experimental data at high carbon dioxide pressures and high salinities make verification of model results difficult. Results indicate standalone solubility models that do not take mineral reactions into account will underestimate the total capacity of aquifers to sequester carbon dioxide in the long term through enhanced solubility and mineral trapping mechanisms. Overall, it is difficult to confidently predict the ultimate sequestration capacity of deep saline aquifers using geochemical models. (author)

Geochemical prospect ion results of Treinta y Tres aerial photo

International Nuclear Information System (INIS)

Zeegers, H.; Bonnefoy, D.; Garau, M.; Spangenberg, J.

1981-01-01

This report shows the geochemical prospect ion results carried out within the framework of the multielemental geochemical strategy. The samples were studied by e spectrometry in the laboratories of Orleans.

Determining Changes in Groundwater Quality during Managed Aquifer Recharge

Science.gov (United States)

Gambhir, T.; Houlihan, M.; Fakhreddine, S.; Dadakis, J.; Fendorf, S. E.

2016-12-01

Managed aquifer recharge (MAR) is becoming an increasingly prevalent technology for improving the sustainability of freshwater supply. However, recharge water can alter the geochemical conditions of the aquifer, mobilizing contaminants native to the aquifer sediments. Geochemical alterations on deep (>300 m) injection of highly treated recycled wastewater for MAR has received limited attention. We aim to determine how residual disinfectants used in water treatment processes, specifically the strong oxidants chloramine and hydrogen peroxide, affect metal mobilization within deep injection wells of the Orange County Water District. Furthermore, as the treated recharge water has very low ionic strength (44.6 mg L-1 total dissolved solids), we tested how differing concentrations of magnesium chloride and calcium chloride affected metal mobilization within deep aquifers. Continuous flow experiments were conducted on columns dry packed with sediments from a deep injection MAR site in Orange County, CA. The effluent was analyzed for shifts in water quality, including aqueous concentrations of arsenic, uranium, and chromium. Interaction between the sediment and oxic recharge solution causes naturally-occurring arsenopyrite to repartition onto iron oxides. The stability of arsenic on the newly precipitated iron oxides is dependent on pH changes during recharge.

Characterizing a complex aquifer system using geophysics, hydrodynamics and geochemistry: A new distribution of Miocene aquifers in the Zéramdine and Mahdia-Jébéniana blocks (east-central Tunisia)

Science.gov (United States)

Lachaal, Fethi; Bédir, Mourad; Tarhouni, Jamila; Gacha, Ayadi Ben; Leduc, Christian

2011-06-01

The Zéramdine and Mahdia-Jébéniana blocks are located in the Sahel region in east-central Tunisia. Active tectonics have divided the region into numerous sub-units, as result of multiple phases of distension and compression. The Miocene fluvio-deltaic sediment sandy layers have aquiferous capacities but their hydraulic properties are still unknown, due to the lack of investigation wells. This study proposes a new description of the regional hydrogeology of Miocene deposits. Seismic-reflection and wireline logging of petroleum and water wells were used to understand the structure and the geometry of the Miocene reservoirs. The groundwater flow and its relationship to the sedimentary and tectonic context were then identified by studying piezometry and hydrochemistry. Two Miocene deep aquifer systems were identified: (1) Zéramdine-Béni Hassen to the north and (2) Jébéniana-Ksour Essef to the south. These aquifers are separated by the Mahdia graben. Other major tectonic structures, such as the Zéramdine fault corridor, the Moknine graben, and the El-Jem half-graben represent lateral boundaries for these aquifers. Other deeper sandy and clayey-sandy reservoirs were also identified in the area. Their repartition, thickness and depth vary from one block to other. Hydrodynamics of the deep aquifers seems to be controlled by geological structures. Two independent compartments were identified: in the northern block groundwater flows from West to East and from Northwest to Southeast, while in the southern block it flows from Northwest to Southeast. Geochemical facies are of two types: Na-Ca-Cl-SO 4 for the Zéramdine-Béni Hassen deep aquifer and Na-Cl for the Jébéniana-Ksour Essef deep aquifer. The hydrodynamic and geochemical results confirm the sharing of the Miocene sediments into two aquifers.

Impact of Varying Wave Conditions on the Mobility of Arsenic in a Nearshore Aquifer on the Great Lakes

Science.gov (United States)

Rakhimbekova, S.; O'Carroll, D. M.; Robinson, C. E.

2017-12-01

Groundwater-coastal water interactions play an important role in controlling the behavior of inorganic chemicals in nearshore aquifers and the subsequent flux of these chemicals to receiving coastal waters. Previous studies have shown that dynamic groundwater flows and water exchange across the sediment-water interface can set up strong geochemical gradients and an important reaction zone in a nearshore aquifer that affect the fate of reactive chemicals. There is limited understanding of the impact of transient coastal forcing such as wave conditions on groundwater dynamics and geochemistry in a nearshore aquifer. The goal of this study was to assess the impact of intensified wave conditions on the behavior of arsenic in a nearshore aquifer and to determine the hydrological and geochemical factors controlling its fate and ultimate delivery to receiving coastal waters. Field investigations were conducted over the period of intensified wave conditions on a freshwater beach on Lake Erie, Canada. High spatial resolution aqueous and sediment sampling was conducted to characterize the subsurface distribution of inorganic species in the nearshore aquifer. Numerical groundwater flow and transport simulations were conducted to evaluate wave-induced perturbations in the flow dynamics including characterizing changes in the groundwater flow recirculations in the nearshore aquifer. The combination of field data and numerical simulations reveal that varying wave conditions alter groundwater flows and set up geochemical transition zones within the aquifer resulting in the release and sequestration of arsenic. Interactions between oxic surface water, mildly reducing shallow groundwater, and reducing sulfur- and iron-rich deep groundwater promote dynamic iron, sulfur and manganese cycling which control the mobility of arsenic in the aquifer. The findings of this study have potential implications for the fate and transport of other reactive chemicals (e.g. phosphorus, mercury) in

Geochemical and Isotopic Characteristics of Quaternary Aquifer in Sohag District, Upper Egypt

International Nuclear Information System (INIS)

Ahmed, M.A.

2008-01-01

Thc Nile River valley represent one of the most important regions for agriculture and land reclamation in our area. Environmental isotopes and hydrochemical compositions in conjunction with geological and hydrogeological data were used to define chemical characteristics, sources of salinity, ground water origin and the possible recharge sources to the Nile Valley aquifer in Sohag district, Upper Egypt. The total dissolved solids of the ground water samples have higher values (445-7828 mg/L) than surface water (291-348 mg/L). The ground water in the Nile flood plain is very similar to that of the river water except at the margins of the basin. This ground water contains isotopic contents comparable to the river Nile with low TDS. The change of water quality at the old alluvium plain could be due to extensive use of fertilizers to improve soil characteristics in new reclamation area. Mineral saturation indices suggest that the dissolution of evaporites and halite is significant in the ground water and responsible for most of the ground water salinization. The relationships between Na + ,Cl - , Ca 2+ , Mg 2+ ,HCO 3 - and SO 4 2- show that complex geochemical processes control the chemical history of ground water: (I) continuous dissolution of evaporites and halite and precipitation of carbonate rocks, (2) cation exchange between ground water and clay minerals, (3) excessive use of fertilizers rich in MgSO 4 in the reclamation projects. The isotopic contents of surface water raged from 2.03 to 2.93%0 for δ 18 O, from 15.3 to 28.4%0 for δ 3 H, and from 4.6 to 7.8 TU for tritium while the isotopic contents of ground water ranged from -8,41 to 3,86% o for δ 18 O, from -67.8 to 29.9%0 for δ 2 H, and from 0.5 to 11.3 TU for tritium. The isotopic data reveals that the rechargability of this water is attributed to Nile flood water which was depleted in its isotopic content. Significant contribution from the palaeowater, which stored in the Nubia sandstone aquifer system

Land-use change and managed aquifer recharge effects on the hydrogeochemistry of two contrasting atoll island aquifers, Roi-Namur Island, Republic of the Marshall Islands

International Nuclear Information System (INIS)

Hejazian, Mehrdad; Gurdak, Jason J.; Swarzenski, Peter; Odigie, Kingsley O.; Storlazzi, Curt D.

2017-01-01

Freshwater resources on low-lying atoll islands are highly vulnerable to climate change and sea-level rise. In addition to rainwater catchment, groundwater in the freshwater lens is a critically important water resource on many atoll islands, especially during drought. Although many atolls have high annual rainfall rates, dense natural vegetation and high evapotranspiration rates can limit recharge to the freshwater lens. Here we evaluate the effects of land-use/land-cover change and managed aquifer recharge on the hydrogeochemistry and supply of groundwater on Roi-Namur Island, Republic of the Marshall Islands. Roi-Namur is an artificially conjoined island that has similar hydrogeology on the Roi and Namur lobes, but has contrasting land-use/land-cover and managed aquifer recharge only on Roi. Vegetation removal and managed aquifer recharge operations have resulted in an estimated 8.6 × 10"5 m"3 of potable groundwater in the freshwater lens on Roi, compared to only 1.6 × 10"4 m"3 on Namur. We use groundwater samples from a suite of 33 vertically nested monitoring wells, statistical testing, and geochemical modeling using PHREEQC to show that the differences in land-use/land-cover and managed aquifer recharge on Roi and Namur have a statistically significant effect on several groundwater-quality parameters and the controlling geochemical processes. Results also indicate a six-fold reduction in the dissolution of carbonate rock in the freshwater lens and overlying vadose zone of Roi compared to Namur. Mixing of seawater and the freshwater lens is a more dominant hydrogeochemical process on Roi because of the greater recharge and flushing of the aquifer with freshwater as compared to Namur. In contrast, equilibrium processes and dissolution-precipitation non-equilibrium reactions are more dominant on Namur because of the longer residence times relative to the rate of geochemical reactions. Findings from Roi-Namur Island support selective land

Hydrogeophysics and geochemistry reveal heterogeneity and water quality improvements in aquifer recharge and recovery (ARR) (Invited)

Science.gov (United States)

Parsekian, A.; Regnery, J.; Wing, A.; Knight, R. J.; Drewes, J. E.

2013-12-01

Aquifer recharge and recover (ARR) is the process of infiltrating water into the ground for storage and withdrawal through wells at a later time. Two significant challenges faced during the design of ARR systems are 1) evaluating aquifer heterogeneity and 2) understanding the rock fluid interactions; these knowledge gaps may have profound impacts on the volume of recoverable water and the improvement in water quality in comparison with the source-water. Our objective in this research is to leverage the advantages of hydrogeophysical measurements and geochemical sampling to reveal the properties of an aquifer through which ARR water travels with the goal of informing current operations and future design decisions. Combined geophysical and geochemical investigations reveal subsurface heterogeneity, indicate possible flow paths though the aquifer and quantify specific reductions in contaminant concentrations. Ground penetrating radar (GPR), electromagnetic induction (EMI) and electrical resistivity tomography (ERT) were used to image the subsurface throughout two key infiltration/extraction areas of an ARR site in Colorado, USA. The most valuable results came from 2.5D ERT revealing the structural patterns and suggesting the distribution of textural composition of unconsolidated sediments. Geochemical measurements on transects intersecting the geophysical measurements resolved bulk parameters (i.e. total organic carbon, cations, anions) and trace organic contaminants (e.g. trace organic compounds) and were also used to estimate mixing and water travel times and assess the performance of the ARR site regarding water quality and quantity. Our results indicate that the subsurface is highly heterogeneous at our study site and that the coarse-grained sedimentary units, acting as the best conduit for transporting water, are likely discontinuous. The electrical resistivity measurements indicate certain areas of the infiltration basins may have good hydraulic connections to

Geochemical and isotopic tracers of recharge and reclamation of stormwater in an urban aquifer: Adelaide, South Australia

International Nuclear Information System (INIS)

Herczeg, A.L.; Rattray, K.J.; Dillon, P.J.; Pavelic, P.C.; Barry, K.J.

2002-01-01

Artificial recharge and reclamation of stormwater into groundwater is a newly developing strategy to augment water resources in the Adelaide metropolitan area of South Australia. Mixing between injected storm water and native groundwater can be most effectively using naturally occurring chloride ion. Stable isotopes of the water molecule are used more effectively during short term tests (i.e., immediately following injection events), and requires frequent monitoring of the surface water end-member. Biogeochemical processes involving geochemical reactions such as organic matter oxidation, carbonate mineral dissolution and sulfide mineral oxidation are very effectively traced by δ 13 C and 14 C (of TDIC) and δ 34 S (of SO 4 2- ). The most important processes occurring in the Tertiary limestone aquifer in Adelaide were carbonate mineral dissolution which is induced largely by CO 2 production during organic matter oxidation. Sulfide mineral oxidation is a minor process, and is accompanied by an equivalent amount of sulfate reduction after injection of the stormwater. (author)

Assessment of Managed Aquifer Recharge through Modeling—A Review

Directory of Open Access Journals (Sweden)

Jana Ringleb

2016-12-01

Full Text Available Managed aquifer recharge (MAR is the purposeful recharge of an aquifer for later recovery or environmental benefits and represents a valuable method for sustainable water resources management. Models can be helpful tools for the assessment of MAR systems. This review encompasses a survey and an analysis of case studies which apply flow and transport models to evaluate MAR. The observed modeling objectives include the planning or optimization of MAR schemes as well as the identification and quantification of geochemical processes during injection, storage and recovery. The water recovery efficiency and the impact of the injected water on the ambient groundwater are further objectives investigated in the reviewed studies. These objectives are mainly solved by using groundwater flow models. Unsaturated flow models, solute transport models, reactive geochemical models as well as water balance models are also frequently applied and often coupled. As each planning step to setup a new MAR facility requires cost and time investment, modeling is used to minimize hazard risks and assess possible constraints of the system such as low recovery efficiency, clogging and geochemical processes.

Insights from the salinity origins and interconnections of aquifers in a regional scale sedimentary aquifer system (Adour-Garonne district, SW France): Contributions of δ34S and δ18O from dissolved sulfates and the 87Sr/86Sr ratio

International Nuclear Information System (INIS)

Brenot, Agnès; Négrel, Philippe; Petelet-Giraud, Emmanuelle; Millot, Romain; Malcuit, Eline

2015-01-01

Highlights: • Regional sedimentary aquifer on the Aquitaine Basin (SW France). • Dealing with limited number of groundwater wells available. • Strong control of evaporite dissolution on groundwater dissolved elements. • Guidelines for decision-makers to manage water resources. - Abstract: The multi-layered Eocene aquifer is a regional scale sedimentary aquifer system occupying ∼120,000 km 2 within the Adour-Garonne district (France). Local authorities have recently identified the aquifer as being at risk from extensive irrigation abstractions, threatening the sustainability of this key resource. Because large water abstractions for human activities can significantly influence the natural functioning of such aquifer systems, e.g., with leakage between aquifer layers, which can lead to water quality degradation, the characterization of such large systems constitutes a key point to protect and prevent further deterioration of aquatic ecosystems. This study provides further insight on this large aquifer through a geochemical approach, which addresses the limited number of groundwater wells where sampling is possible. For that purpose, a geochemical analysis combining two isotope systems (δ 34 S SO4 , δ 18 O SO4 and 87 Sr/ 86 Sr) has been applied. The Eocene sedimentary aquifer system (detrital to carbonate deposits) is made up of four aquifer layers, Eocene Infra-Molassic sand, Early Eocene, Middle Eocene and Late Eocene, and has a mineralized area north of the Aquitaine Basin, where groundwater shows strong mineralization and anomalous levels of critical substances (SO 4 , F, etc.), increasing the difficulty of resource exploitation. The extreme heterogeneity of the geochemical composition of the groundwater between the aquifers and within a single aquifer is discussed in terms of the lithological control induced by the lateral variation of facies and interconnections between aquifer layers. Geochemical tools, especially the δ 34 S and δ 18 O from

Microbial diversity and impact on carbonate geochemistry across a changing geochemical gradient in a karst aquifer.

Science.gov (United States)

Gray, Cassie J; Engel, Annette S

2013-02-01

Although microbes are known to influence karst (carbonate) aquifer ecosystem-level processes, comparatively little information is available regarding the diversity of microbial activities that could influence water quality and geological modification. To assess microbial diversity in the context of aquifer geochemistry, we coupled 16S rRNA Sanger sequencing and 454 tag pyrosequencing to in situ microcosm experiments from wells that cross the transition from fresh to saline and sulfidic water in the Edwards Aquifer of central Texas, one of the largest karst aquifers in the United States. The distribution of microbial groups across the transition zone correlated with dissolved oxygen and sulfide concentration, and significant variations in community composition were explained by local carbonate geochemistry, specifically calcium concentration and alkalinity. The waters were supersaturated with respect to prevalent aquifer minerals, calcite and dolomite, but in situ microcosm experiments containing these minerals revealed significant mass loss from dissolution when colonized by microbes. Despite differences in cell density on the experimental surfaces, carbonate loss was greater from freshwater wells than saline, sulfidic wells. However, as cell density increased, which was correlated to and controlled by local geochemistry, dissolution rates decreased. Surface colonization by metabolically active cells promotes dissolution by creating local disequilibria between bulk aquifer fluids and mineral surfaces, but this also controls rates of karst aquifer modification. These results expand our understanding of microbial diversity in karst aquifers and emphasize the importance of evaluating active microbial processes that could affect carbonate weathering in the subsurface.

Natural and EDTA-complexed lanthanides used as a geochemical probe for aquifers: a case study of Orleans valley's alluvial and karstic aquifers

International Nuclear Information System (INIS)

Le Borgne, F.; Treuil, M.; Joron, J.L.; Lepiller, M.

2005-01-01

channels direction. During the river descent, horizontal flows are quasi absent and migrations are mainly vertical from the alluvia down to the calcareous part of the aquifer. Due to those hydrodynamic characteristics, alluvia and non fissured limestone have a high dynamic confining capacity. Elements with high affinity for solid or colloidal phases (e.g. light Ln) have an increased confining capacity in the whole aquifer, by sorption and colloid filtration within the alluvia and at the alluvial-calcareous interface, and by colloid decanting within the karstic channels. Overall, this model combines two components. The first one, hydrodynamical, results from the repartition of the loads pulsed by river Loire through the karst. The second one, physico-chemical, results from the element distribution mainly controlled by colloid/solute complexes exchange coefficients. (authors)

Review of simulation techniques for Aquifer Thermal Energy Storage (ATES)

Science.gov (United States)

Mercer, J. W.; Faust, C. R.; Miller, W. J.; Pearson, F. J., Jr.

1981-03-01

The analysis of aquifer thermal energy storage (ATES) systems rely on the results from mathematical and geochemical models. Therefore, the state-of-the-art models relevant to ATES were reviewed and evaluated. These models describe important processes active in ATES including ground-water flow, heat transport (heat flow), solute transport (movement of contaminants), and geochemical reactions. In general, available models of the saturated ground-water environment are adequate to address most concerns associated with ATES; that is, design, operation, and environmental assessment. In those cases where models are not adequate, development should be preceded by efforts to identify significant physical phenomena and relate model parameters to measurable quantities.

Relationship of regional water quality to aquifer thermal energy storage

Energy Technology Data Exchange (ETDEWEB)

Allen, R.D.

1983-11-01

Ground-water quality and associated geologic characteristics may affect the feasibility of aquifer thermal energy storage (ATES) system development in any hydrologic region. This study sought to determine the relationship between ground-water quality parameters and the regional potential for ATES system development. Information was collected from available literature to identify chemical and physical mechanisms that could adversely affect an ATES system. Appropriate beneficiation techniques to counter these potential geochemical and lithologic problems were also identified through the literature search. Regional hydrology summaries and other sources were used in reviewing aquifers of 19 drainage regions in the US to determine generic geochemical characteristics for analysis. Numerical modeling techniques were used to perform geochemical analyses of water quality from 67 selected aquifers. Candidate water resources regions were then identified for exploration and development of ATES. This study identified six principal mechanisms by which ATES reservoir permeability may be impaired: (1) particulate plugging, (2) chemical precipitation, (3) liquid-solid reactions, (4) formation disaggregation, (5) oxidation reactions, and (6) biological activity. Specific proven countermeasures to reduce or eliminate these effects were found. Of the hydrologic regions reviewed, 10 were identified as having the characteristics necessary for ATES development: (1) Mid-Atlantic, (2) South-Atlantic Gulf, (3) Ohio, (4) Upper Mississippi, (5) Lower Mississippi, (6) Souris-Red-Rainy, (7) Missouri Basin, (8) Arkansas-White-Red, (9) Texas-Gulf, and (10) California.

Palaeoclimatic trends deduced from the hydrochemistry of a Triassic sandstone aquifer, U.K

International Nuclear Information System (INIS)

Bath, A.H.; Edmunds, W.M.; Andrews, J.N.

1978-01-01

A detailed geochemical study (elemental, isotopic and dissolved inert gases) of unconfined and confined sections of the Triassic non-marine sandstone aquifer in Eastern England has been undertaken. Aspects of the recharge history of this aquifer over the past 40 000 years are revealed by examination of the data. (orig./HK) [de

Geochemical and statistical evidence of recharge, mixing, and controls on spring discharge in an eogenetic karst aquifer

Science.gov (United States)

Moore, Paul J.; Martin, Jonathan B.; Screaton, Elizabeth J.

2009-10-01

SummaryInformation about sources of recharge, distributions of flow paths, and the extent of water-rock reactions in karst aquifers commonly result from monitoring spring chemistry and discharge. To investigate the relationship between spring characteristics and the complexities of karst aquifers, we couple variations in surface- and groundwater chemistry to physical conditions including river stage, precipitation, and evapotranspiration (ET) within a sink-rise system through a 6-km portion of the Upper Floridan aquifer (UFA) in north-central Florida. Principal component analysis (PCA) of time series major-element compositions suggests that at least three sources of water affect spring discharge, including allogenic recharge into a swallet, diffuse recharge through a thin vadose zone, and water upwelling from deep within the aquifer. The deep-water source exerts the strongest influence on water chemistry by providing a majority of Na +, Mg 2+, K +, Cl -, and SO42- to the system. Anomalously high temperature at one of several monitoring wells reflects vertical flow of about 1 m/year. Mass-balance calculations suggest diffuse recharge and deep-water upwelling can provide up to 50% of the spring discharge; however, their contributions depend on head gradients between the conduit and surrounding aquifer matrix, which are influenced by variations in precipitation, ET, and river stage. Our results indicate that upwelling from deep flow paths may provide significant contributions of water to spring discharge, and that monitoring only springs limits interpretations of karst systems by masking critical components of the aquifer, such as water sources and flow paths. These results also suggest the matrix in eogenetic aquifers is a major pathway for flow even in a system dominated by conduits.

Monitoring active volcanoes: The geochemical approach

Directory of Open Access Journals (Sweden)

Takeshi Ohba

2011-06-01

Full Text Available

The geochemical surveillance of an active volcano aims to recognize possible signals that are related to changes in volcanic activity. Indeed, as a consequence of the magma rising inside the volcanic "plumbing system" and/or the refilling with new batches of magma, the dissolved volatiles in the magma are progressively released as a function of their relative solubilities. When approaching the surface, these fluids that are discharged during magma degassing can interact with shallow aquifers and/or can be released along the main volcano-tectonic structures. Under these conditions, the following main degassing processes represent strategic sites to be monitored.

The main purpose of this special volume is to collect papers that cover a wide range of topics in volcanic fluid geochemistry, which include geochemical characterization and geochemical monitoring of active volcanoes using different techniques and at different sites. Moreover, part of this volume has been dedicated to the new geochemistry tools.

Effect of transient wave forcing on the behavior of arsenic in a sandy nearshore aquifer

Science.gov (United States)

Rakhimbekova, S.; O'Carroll, D. M.; Robinson, C. E.

2016-12-01

Waves cause large quantities of coastal water to recirculate across the groundwater-coastal water interface in addition to inducing complex groundwater flows in the nearshore aquifer. Due to the distinct chemical composition of recirculating coastal water compared with discharging terrestrial groundwater, wave-induced recirculations and flows can alter geochemical gradients in the nearshore aquifer which may subsequently affect the mobilization and transport of reactive pollutants (e.g., arsenic). The impact of seasonal geochemical and hydrological variability on the occurrence and mobility of arsenic near the groundwater-surface water interface has been shown previously in riverine settings, however, the impact of high frequency geochemical variations (e.g., varying wave conditions) on arsenic mobility in groundwater-surface water environments is unclear. The objective of the study was to assess the impact of intensified wave conditions on the behavior of arsenic in a nearshore aquifer to determine the factors regulating its mobility and transport to receiving coastal waters. Field investigations were conducted at a permeable beach on the Great Lakes during a period of intensified wave conditions (wave event). High spatial resolution pore water sampling captured the geochemical conditions in the nearshore aquifer prior to the wave event, immediately after the wave event and over a recovery period of 3 weeks following the wave event. Shifts in pH and redox potential (ORP) gradients in response to varying wave conditions caused shifts in the iron and arsenic distributions in the aquifer. Sediment analysis was combined with the pore water distributions to assess the release of sediment-bound arsenic in response to the varying wave conditions. Insight into the effect of transient forcing on arsenic mobility and transport in groundwater-surface water environments is important for evaluating the potential risks associated with this toxic metalloid. The findings of this

Seawater intrusion in the gravelly confined aquifer of the coastal Pisan Plain (Tuscany): hydrogeological and geochemical investigation to assess causes and consequences

Science.gov (United States)

Doveri, M.; Giannecchini, R.; Butteri, M.

2012-12-01

The gravelly horizon of the Pisa plain multilayered system is a confined aquifer tapped by a large number of wells. It hosts a very important water resource for drinking, industrial and irrigable uses, but may be affected by seawater intrusion coming from the coastal area; most wells is distributed inland, anyway a significant exploitation along the coastal area is also present to supply farms and tourist services. Previous hydrogeological and geochemical investigations carried out in coastal area stated maximum percentage of seawater in gravelly aquifer of about 7-9% and suggested the presence of two different mechanisms (Doveri et alii, 2010): i) a direct seawater intrusion from the zone where the gravelly aquifer is in contact with the sea floor; ii) a mixing process between freshwater and seawater, the latter deriving from the Arno river-shallow sandy aquifer system. Basing on these results, since January 2012 a new two-year project was financed by the MSRM Regional Park. Major aims are a better definition of such phenomena and their distribution on the territory, and an assessing of the seawater intrusion trend in relation to groundwater exploitation. Eleven piezometers were realised during first semester of 2012, thus improving the measurement network, which is now made up by 40 wells/piezometers distributed on about 60 km^2. Comparing new and previous borehole data a general confinement of the gravelly aquifer is confirmed, excepting in the northern part where the aquifer is in contact with the superficial sandy one. Preliminary field measurement was performed in June 2012, during which water level (WL) and electrical conductivity (EC) data were collected. WLs below the sea-level were observed on most of the studied area, with a minimum value of about -5 m a.s.l. in the inner part of the northern zone, where major exploitation is present. Moreover, a relative minimum of WL (about -2 m a.s.l.) is present near the shoreline in the southern zone. In the latter

Groundwater geochemistry of a Mio-Pliocene aquifer in the northeastern Algerian Sahara (Djamaa region)

Science.gov (United States)

Houari, Idir Menad; Nezli, Imed Eddine; Belksier, Mohamed Salah

2018-05-01

The groundwater resources in the Northern Sahara are represented by two superimposed major aquifer systems: the Intercalary Continental (CI) and the Terminal Complex (CT). The waters of these aquifers pose serious physical and chemical quality problems; they are highly mineralized and very hard. The present work aims to describe the water's geochemical evolution of sand groundwater (Mio-Pliocene) of the Terminal Complex in the area of Djamaa, by the research of the relationship between water's chemical composition and lithology of aquifer formations through. The results obtained show that the water's chemistry is essentially governed by the dissolution of evaporate formations, which gives to, waters an excessive mineralization expressed by high concentrations of sulfates, chlorides and sodium.

Instrumenting caves to collect hydrologic and geochemical data: case study from James Cave, Virginia

Science.gov (United States)

Schreiber, Madeline E.; Schwartz, Benjamin F.; Orndorff, William; Doctor, Daniel H.; Eagle, Sarah D.; Gerst, Jonathan D.

2015-01-01

Karst aquifers are productive groundwater systems, supplying approximately 25 % of the world’s drinking water. Sustainable use of this critical water supply requires information about rates of recharge to karst aquifers. The overall goal of this project is to collect long-term, high-resolution hydrologic and geochemical datasets at James Cave, Virginia, to evaluate the quantity and quality of recharge to the karst system. To achieve this goal, the cave has been instrumented for continuous (10-min interval) measurement of the (1) temperature and rate of precipitation; (2) temperature, specific conductance, and rate of epikarst dripwater; (3) temperature of the cave air; and (4) temperature, conductivity, and discharge of the cave stream. Instrumentation has also been installed to collect both composite and grab samples of precipitation, soil water, the cave stream, and dripwater for geochemical analysis. This chapter provides detailed information about the instrumentation, data processing, and data management; shows examples of collected datasets; and discusses recommendations for other researchers interested in hydrologic and geochemical monitoring of cave systems. Results from the research, briefly described here and discussed in more detail in other publications, document a strong seasonality of the start of the recharge season, the extent of the recharge season, and the geochemistry of recharge.

Characterisation of organic matter associated with groundwater arsenic in reducing aquifers of southwestern Taiwan.

Science.gov (United States)

Al Lawati, Wafa M; Jean, Jiin-Shuh; Kulp, Thomas R; Lee, Ming-Kuo; Polya, David A; Liu, Chia-Chuan; van Dongen, Bart E

2013-11-15

Arsenic (As) in groundwaters extensively used by people across the world constitutes a serious public health threat. The importance of organic matter (OM) as an electron donor in microbially-mediated reduction of As(V) or Fe(III)-bearing As-host minerals leading to mobilisation of solid-phase arsenic is widely recognised. Notwithstanding this, there are few studies characterising OM in such aquifers and, in particular, there is a dearth of data from the classic arsenic bearing aquifers in southwestern Taiwan. Organic geochemical analyses of sediments from a known groundwater arsenic hot-spot in southwestern Taiwan revealed contributions of thermally mature and plant derived origin, consistent with OM sources in all other Asian groundwater aquifer sediments analysed to date, indicating comparable sources and routes of OM transfer. The combined results of amended As(V) reduction assays with the organic geochemical analysis revealed that the microbiological process of dissimilatory As(V) reduction is active in this aquifer, but it is not controlled by a specific source of analysed OM. These indicate that (i) part of the OM that was considered to be less bio-available could still be used as an electron donor or (ii) other electron donors, not analysed in present study, could be controlling the rate of As release. Copyright © 2012 Elsevier B.V. All rights reserved.

Geochemical prospect ion results of Mariscala aerial photo

International Nuclear Information System (INIS)

Filippini, J.

1989-01-01

This report shows the geochemical prospect ion results carried out within the framework of the metalical mining prospect ion in Mariscala aerial photo. Lavalleja district belong to the Mining inventory programme of Uruguay.

Characterisation of organic matter associated with groundwater arsenic in reducing aquifers of southwestern Taiwan

Energy Technology Data Exchange (ETDEWEB)

Al Lawati, Wafa M. [School of Earth, Atmospheric and Environmental Sciences, Williamson Research Centre for Molecular Environmental Science, University of Manchester, Manchester (United Kingdom); Higher College of Technology, Ministry of Manpower, Muscat (Oman); Jean, Jiin-Shuh [Department of Earth Sciences, National Cheng Kung University, 1 University Road, Tainan 701, Taiwan (China); Kulp, Thomas R. [Department of Earth Sciences and Environmental Studies, State University of New York, Binghamton, NY (United States); Lee, Ming-Kuo [Department of Geology and Geography, Auburn University, Auburn, AL (United States); Polya, David A. [School of Earth, Atmospheric and Environmental Sciences, Williamson Research Centre for Molecular Environmental Science, University of Manchester, Manchester (United Kingdom); Liu, Chia-Chuan [Department of Earth Sciences, National Cheng Kung University, 1 University Road, Tainan 701, Taiwan (China); Dongen, Bart E. van, E-mail: Bart.vanDongen@manchester.ac.uk [School of Earth, Atmospheric and Environmental Sciences, Williamson Research Centre for Molecular Environmental Science, University of Manchester, Manchester (United Kingdom)

2013-11-15

Highlights: ► First lipid analysis of Taiwanese aquifer sediments from groundwater As-prone region. ► Both plant-derived terrestrial and mature hydrocarbon lipid sources identified. ► Organic matter sources similar to those of other high As groundwater aquifers. ► Groundwater arsenic at depth controlled by biotic As mobilisation processes. ► Biotic As mobilisation not controlled by a specific source of analysed organic matter. -- Abstract: Arsenic (As) in groundwaters extensively used by people across the world constitutes a serious public health threat. The importance of organic matter (OM) as an electron donor in microbially-mediated reduction of As(V) or Fe(III)-bearing As-host minerals leading to mobilisation of solid-phase arsenic is widely recognised. Notwithstanding this, there are few studies characterising OM in such aquifers and, in particular, there is a dearth of data from the classic arsenic bearing aquifers in southwestern Taiwan. Organic geochemical analyses of sediments from a known groundwater arsenic hot-spot in southwestern Taiwan revealed contributions of thermally mature and plant derived origin, consistent with OM sources in all other Asian groundwater aquifer sediments analysed to date, indicating comparable sources and routes of OM transfer. The combined results of amended As(V) reduction assays with the organic geochemical analysis revealed that the microbiological process of dissimilatory As(V) reduction is active in this aquifer, but it is not controlled by a specific source of analysed OM. These indicate that (i) part of the OM that was considered to be less bio-available could still be used as an electron donor or (ii) other electron donors, not analysed in present study, could be controlling the rate of As release.

Characterisation of organic matter associated with groundwater arsenic in reducing aquifers of southwestern Taiwan

International Nuclear Information System (INIS)

Al Lawati, Wafa M.; Jean, Jiin-Shuh; Kulp, Thomas R.; Lee, Ming-Kuo; Polya, David A.; Liu, Chia-Chuan; Dongen, Bart E. van

2013-01-01

Highlights: ► First lipid analysis of Taiwanese aquifer sediments from groundwater As-prone region. ► Both plant-derived terrestrial and mature hydrocarbon lipid sources identified. ► Organic matter sources similar to those of other high As groundwater aquifers. ► Groundwater arsenic at depth controlled by biotic As mobilisation processes. ► Biotic As mobilisation not controlled by a specific source of analysed organic matter. -- Abstract: Arsenic (As) in groundwaters extensively used by people across the world constitutes a serious public health threat. The importance of organic matter (OM) as an electron donor in microbially-mediated reduction of As(V) or Fe(III)-bearing As-host minerals leading to mobilisation of solid-phase arsenic is widely recognised. Notwithstanding this, there are few studies characterising OM in such aquifers and, in particular, there is a dearth of data from the classic arsenic bearing aquifers in southwestern Taiwan. Organic geochemical analyses of sediments from a known groundwater arsenic hot-spot in southwestern Taiwan revealed contributions of thermally mature and plant derived origin, consistent with OM sources in all other Asian groundwater aquifer sediments analysed to date, indicating comparable sources and routes of OM transfer. The combined results of amended As(V) reduction assays with the organic geochemical analysis revealed that the microbiological process of dissimilatory As(V) reduction is active in this aquifer, but it is not controlled by a specific source of analysed OM. These indicate that (i) part of the OM that was considered to be less bio-available could still be used as an electron donor or (ii) other electron donors, not analysed in present study, could be controlling the rate of As release

Potential impacts of leakage from deep CO2 geosequestration on overlying freshwater aquifers.

Science.gov (United States)

Little, Mark G; Jackson, Robert B

2010-12-01

Carbon Capture and Storage may use deep saline aquifers for CO(2) sequestration, but small CO(2) leakage could pose a risk to overlying fresh groundwater. We performed laboratory incubations of CO(2) infiltration under oxidizing conditions for >300 days on samples from four freshwater aquifers to 1) understand how CO(2) leakage affects freshwater quality; 2) develop selection criteria for deep sequestration sites based on inorganic metal contamination caused by CO(2) leaks to shallow aquifers; and 3) identify geochemical signatures for early detection criteria. After exposure to CO(2), water pH declines of 1-2 units were apparent in all aquifer samples. CO(2) caused concentrations of the alkali and alkaline earths and manganese, cobalt, nickel, and iron to increase by more than 2 orders of magnitude. Potentially dangerous uranium and barium increased throughout the entire experiment in some samples. Solid-phase metal mobility, carbonate buffering capacity, and redox state in the shallow overlying aquifers influence the impact of CO(2) leakage and should be considered when selecting deep geosequestration sites. Manganese, iron, calcium, and pH could be used as geochemical markers of a CO(2) leak, as their concentrations increase within 2 weeks of exposure to CO(2).

Effects of Subsurface Microbial Ecology on Geochemical Evolution of a Crude-Oil Contaminated Aquifer

Science.gov (United States)

Bekins, B. A.; Cozzarelli, I. M.; Godsy, E. M.; Warren, E.; Hostettler, F. D.

2001-12-01

We have identified several subsurface habitats for microorganisms in a crude oil contaminated located near Bemidji, Minnesota. These aquifer habitats include: 1) the unsaturated zone contaminated by hydrocarbon vapors, 2) the zones containing separate-phase crude oil, and 3) the aqueous-phase contaminant plume. The surficial glacial outwash aquifer was contaminated when a crude oil pipeline burst in 1979. We analyzed sediment samples from the contaminated aquifer for the most probable numbers of aerobes, iron reducers, fermenters, and three types of methanogens. The microbial data were then related to gas, water, and oil chemistry, sediment extractable iron, and permeability. The microbial populations in the various contaminated subsurface habitats each have special characteristics and these affect the aquifer and contaminant chemistry. In the eight-meter-thick, vapor-contaminated vadose zone, a substantial aerobic population has developed that is supported by hydrocarbon vapors and methane. Microbial numbers peak in locations where access to both hydrocarbons and nutrients infiltrating from the surface is maximized. The activity of this population prevents hydrocarbon vapors from reaching the land surface. In the zone where separate-phase crude oil is present, a consortium of methanogens and fermenters dominates the populations both above and below the water table. Moreover, gas concentration data indicate that methane production has been active in the oily zone since at least 1986. Analyses of the extracted separate-phase oil show that substantial degradation of C15 -C35 n-alkanes has occurred since 1983, raising the possibility that significant degradation of C15 and higher n-alkanes has occurred under methanogenic conditions. However, lab and field data suggest that toxic inhibition by crude oil results in fewer acetate-utilizing methanogens within and adjacent to the separate-phase oil. Data from this and other sites indicate that toxic inhibition of

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

Energy Technology Data Exchange (ETDEWEB)

Lucas, Y., E-mail: yann.lucas@eost.u-strasbg.fr [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France); Schmitt, A.D., E-mail: anne-desiree.schmitt@univ-fcomte.fr [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France)] [Universite de Franche-Comte et CNRS-UMR 6249, Chrono-Environnement, 16, Route de Gray, 25030 Besancon Cedex (France); Chabaux, F., E-mail: francois.chabaux@eost.u-strasbg.fr [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France); Clement, A.; Fritz, B. [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France); Elsass, Ph. [BRGM, GEODERIS, 1, rue Claude Chappe, 57070 Metz (France); Durand, S. [Universite de Strasbourg et CNRS, Laboratoire d' Hydrologie et de Geochimie de Strasbourg, Ecole et Observatoire des Sciences de la Terre, 1, rue Blessig, 67084 Strasbourg Cedex (France)

2010-11-15

Research highlights: {yields} Major and trace elements along with strontium and uranium isotopic ratios show that groundwater geochemical characteristics along the saline plumes cannot reflect a conservative mixing. {yields} A coupled hydrogeochemical model 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. {yields} The model requires only a small amount of montmorillonite. {yields} It is necessary to consider the pollution history to explain the important chloride, sodium and calcium concentration modifications. {yields} The model shows that the rapidity of the cationic exchange reactions insures a reversibility of the cation fixation on clays in the aquifer. - Abstract: 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

Toward a better understanding of the complex geochemical processes governing subsurface contaminant transport

International Nuclear Information System (INIS)

Puls, R.W.

1990-01-01

Identification and understanding of the geochemical processes, including ion exchange, precipitation, organic partitioning, chemisorption, aqueous complexation, and colloidal stability and transport, controlling subsurface contamination is essential for making accurate predictions of the fate and transport of these constituents. Current approaches to quantify the effect of these processes primarily involve laboratory techniques, including the use of closed static systems (batch experiments) where small amounts of aquifer solids or minerals are contacted with an aqueous phase containing the components of interest for relatively short durations; and dynamic systems (column experiments) where a larger segment of the aquifer is investigated by analyzing the breakthrough profiles of reactive and non-reactive species. Both approaches are constrained by differences in scale, alteration of media during sample collection and use, and spatial variability. More field reactivity studies are needed to complement established laboratory approaches for the determination of retardation factors and scaling factors, corroboration of batch and column results, and validation of sampling techniques. These studies also serve to accentuate areas of geochemical process research where data deficiencies exist, such as the kinetics of adsorption-desorption, metal-organic-mineral interactions, and colloidal mobility. The advantages and disadvantages of the above approaches are discussed in the context of achieving a more completely integrated approach to geochemical transport experiments, with supportive data presented from selected studies. (Author) (16 refs., 4 figs., 2 tabs.)

Arsenic mobilization in an oxidizing alkaline groundwater: Experimental studies, comparison and optimization of geochemical modeling parameters

International Nuclear Information System (INIS)

Hafeznezami, Saeedreza; Lam, Jacquelyn R.; Xiang, Yang; Reynolds, Matthew D.; Davis, James A.; Lin, Tiffany; Jay, Jennifer A.

2016-01-01

Arsenic (As) mobilization and contamination of groundwater affects millions of people worldwide. Progress in developing effective in-situ remediation schemes requires the incorporation of data from laboratory experiments and field samples into calibrated geochemical models. In an oxidizing aquifer where leaching of high pH industrial waste from unlined surface impoundments led to mobilization of naturally occurring As up to 2 mg L −1 , sequential extractions of solid phase As as well as, batch sediment microcosm experiments were conducted to understand As partitioning and solid-phase sorptive and buffering capacity. These data were combined with field data to create a series of geochemical models of the system with modeling programs PHREEQC and FITEQL. Different surface complexation modeling approaches, including component additivity (CA), generalized composite (GC), and a hybrid method were developed, compared and fitted to data from batch acidification experiments to simulate potential remediation scenarios. Several parameters strongly influence the concentration of dissolved As including pH, presence of competing ions (particularly phosphate) and the number of available sorption sites on the aquifer solids. Lowering the pH of groundwater to 7 was found to have a variable, but limited impact (<63%) on decreasing the concentration of dissolved As. The models indicate that in addition to lowering pH, decreasing the concentration of dissolved phosphate and/or increasing the number of available sorption sites could significantly decrease the As solubility to levels below 10 μg L −1 . The hybrid and GC modeling results fit the experimental data well (NRMSE<10%) with reasonable effort and can be implemented in further studies for validation. - Highlights: • Samples were collected from an oxidizing aquifer where high pH waste has led to mobilization of naturally occurring As. • Three surface complexation modeling approaches were used in modeling adsorption

A geochemical and isotopic approach to recharge evaluation in semi-arid zones. Past and present

International Nuclear Information System (INIS)

Edmunds, W.M.; Walton, N.R.G.

1980-01-01

The magnitude of any recharge to aquifers in semi-arid and arid zones is the principal uncertainty in estimating a water balance. Recent studies in Cyprus and Libyan Arab Jamahiriya are currently being used to demonstrate the application of geochemical and isotopic techniques, to the determination of both current and palaeo-recharge. In Cyprus, solute profiles of the unsaturated zone have been interpreted to provide estimates of the direct recharge component using a steady-state, mass-balance approach; results from the chloride profiles compare well with recharge estimates using tritium. In addition, it is found that some solute peaks, notably for specific electrical conductance, give a reasonably accurate record of the rainfall history during the period 1950-1975. The solute profile method is relatively unsophisticated and could be more widely applied to recharge estimation in other semi-arid areas of the world. In Libya, a clear distinction can be made using the combined isotopic, hydrological and geochemical results between regional groundwaters recharged to the upper, unconfined aquifer of the Sirte Basin before 13,000 years BP and younger waters recharged locally during the period 5000-7800 years BP. A well-defined fresh-water channel, superimposed upon the regional water quality pattern, can be traced within the aquifer for some 130 km and represents direct evidence of recharge during the Holocene. Some shallow groundwaters of similar composition to the fresh-water channel are also considered to represent recent, if intermittent, recharge which took place during historical times. It is concluded that geochemical and isotopic studies of both the unsaturated zone and of shallow groundwaters in semi-arid regions, can be used to determine not only the present-day direct recharge component, but also a recharge chronology of immediate historic times, which may be important in the estimation of long-term water resources. (author)

Basement and alluvial aquifers of Malawi: An overview of ...

African Journals Online (AJOL)

Elizabeth B Mapoma

2014-02-17

Feb 17, 2014 ... Rowland HAL, Gault AG, Lythgoe P, Polya DA (2008) Geochemistry of aquifer sediments and arsenic-rich groundwaters from Kandal. Province, Cambodia. Appl. Geochem. 23: 3029–3046. Sajidu SM, Masumbu FFF, Fabiano E, Ngongondo C (2007). Drinking water quality and identification of fluoritic areas ...

Geochemical approach of the salinization mechanisms of coastal aquifers - 14C - 226Ra chronologies

International Nuclear Information System (INIS)

Barbecot, F.

1999-11-01

Through time, coastal aquifers which constitute a great part of available fresh water resources from sedimentary basins in France, were submitted to changes in hydraulic gradients and hydrodynamic properties mainly due to discharge/recharge phases in response to sea level variations and/or anthropic forcing. Performed in the framework of the European program PALAEAUX ('Management of coastal aquifers in Europe, paleo-waters and natural controls'), this work aimed to understand the salinization process originating from the recharge/discharge conditions and recognized in three study aquifers: the calcareous Dogger aquifers along the Channel (Caen area), and the Atlantic coast (Marais Poitevin), and the Astian sandy aquifer (Cap d'Agde). Besides the conventional hydrogeological and hydrochemical methods, the main tools used are those of isotope geochemistry. For the three sites, the modern, fresh groundwaters are marked by the anthropisation of the recharge area. The evolution of isotopic signatures along a flow path depending on the mineralogy of the aquifer matrix, is linked to water-rock interactions such as cation exchange, and equilibrium with aluminosilicates. For the three study sites, the modern fresh groundwaters are marked by the anthropisation of the recharge area. The evolution of isotopic signatures along a flow path depending on the mineralogy of the aquifer matrix, is linked to water-rock interactions such as cation exchange, and equilibrium with aluminosilicates. Residence times of these fresh groundwater are from Present (Atlantic site) up to the 14 C detection limit (Channel site). Groundwater of the Astian aquifer belongs to Holocene, as determined by both 14 C and 226 Ra. From Present to 3 ka, 14 C and 226 Ra ages are coherent. Beyond, the discrepancy observed can be associated to the under-estimation of in- situ 226 Ra production, but more likely, to the 'buffer' effect of the matrix with respect to the 14 C isotopic equilibration. The salty waters

Geomicrobial and Geochemical Redox Processes in a Landfill-Polluted Aquifer

DEFF Research Database (Denmark)

Ludvigsen, Liselotte; Heron, Gorm; Albrechtsen, Hans-Jørgen

1995-01-01

The distribution of different dominant microbial-mediated redox processes in a landfill leachate-polluted aquifer (Grindsted, Denmark) was investigated. The most probable number method was utilized for detecting bacteria able to use each of the electron acceptors, and unamended incubations were u...

A Geochemical Reaction Model for Titration of Contaminated Soil and Groundwater at the Oak Ridge Reservation

Science.gov (United States)

Zhang, F.; Parker, J. C.; Gu, B.; Luo, W.; Brooks, S. C.; Spalding, B. P.; Jardine, P. M.; Watson, D. B.

2007-12-01

This study investigates geochemical reactions during titration of contaminated soil and groundwater at the Oak Ridge Reservation in eastern Tennessee. The soils and groundwater exhibits low pH and high concentrations of aluminum, calcium, magnesium, manganese, various trace metals such as nickel and cobalt, and radionuclides such as uranium and technetium. The mobility of many of the contaminant species diminishes with increasing pH. However, base additions to increase pH are strongly buffered by various precipitation/dissolution and adsorption/desorption reactions. The ability to predict acid-base behavior and associated geochemical effects is thus critical to evaluate remediation performance of pH manipulation strategies. This study was undertaken to develop a practical but generally applicable geochemical model to predict aqueous and solid-phase speciation during soil and groundwater titration. To model titration in the presence of aquifer solids, an approach proposed by Spalding and Spalding (2001) was utilized, which treats aquifer solids as a polyprotic acid. Previous studies have shown that Fe and Al-oxyhydroxides strongly sorb dissolved Ni, U and Tc species. In this study, since the total Fe concentration is much smaller than that of Al, only ion exchange reactions associated with Al hydroxides are considered. An equilibrium reaction model that includes aqueous complexation, precipitation, ion exchange, and soil buffering reactions was developed and implemented in the code HydroGeoChem 5.0 (HGC5). Comparison of model results with experimental titration curves for contaminated groundwater alone and for soil- water systems indicated close agreement. This study is expected to facilitate field-scale modeling of geochemical processes under conditions with highly variable pH to develop practical methods to control contaminant mobility at geochemically complex sites.

Hydrogeochemistry and statistical analysis applied to understand fluoride provenance in the Guarani Aquifer System, Southern Brazil.

Science.gov (United States)

Marimon, Maria Paula C; Roisenberg, Ari; Suhogusoff, Alexandra V; Viero, Antonio Pedro

2013-06-01

High fluoride concentrations (up to 11 mg/L) have been reported in the groundwater of the Guarani Aquifer System (Santa Maria Formation) in the central region of the state of Rio Grande do Sul, Southern Brazil. In this area, dental fluorosis is an endemic disease. This paper presents the geochemical data and the combination of statistical analysis (Principal components and cluster analyses) and geochemical modeling to achieve the hydrogeochemistry of the groundwater and discusses the possible fluoride origin. The groundwater from the Santa Maria Formation is comprised of four different geochemical groups. The first group corresponds to a sodium chloride groundwater which evolves to sodium bicarbonate, the second one, both containing fluoride anomalies. The third group is represented by calcium bicarbonate groundwater, and in the fourth, magnesium is the distinctive parameter. The statistical and geochemical analyses supported by isotopic measurements indicated that groundwater may have originated from mixtures of deeper aquifers and the fluoride concentrations could be derived from rock/water interactions (e.g., desorption from clay minerals).

Numerical simulation of CO2 disposal by mineral trapping in deep aquifers

International Nuclear Information System (INIS)

Xu Tianfu; Apps, John A.; Pruess, Karsten

2004-01-01

Carbon dioxide disposal into deep aquifers is a potential means whereby atmospheric emissions of greenhouse gases may be reduced. However, our knowledge of the geohydrology, geochemistry, geophysics, and geomechanics of CO 2 disposal must be refined if this technology is to be implemented safely, efficiently, and predictably. As a prelude to a fully coupled treatment of physical and chemical effects of CO 2 injection, the authors have analyzed the impact of CO 2 immobilization through carbonate mineral precipitation. Batch reaction modeling of the geochemical evolution of 3 different aquifer mineral compositions in the presence of CO 2 at high pressure were performed. The modeling considered the following important factors affecting CO 2 sequestration: (1) the kinetics of chemical interactions between the host rock minerals and the aqueous phase, (2) CO 2 solubility dependence on pressure, temperature and salinity of the system, and (3) redox processes that could be important in deep subsurface environments. The geochemical evolution under CO 2 injection conditions was evaluated. In addition, changes in porosity were monitored during the simulations. Results indicate that CO 2 sequestration by matrix minerals varies considerably with rock type. Under favorable conditions the amount of CO 2 that may be sequestered by precipitation of secondary carbonates is comparable with and can be larger than the effect of CO 2 dissolution in pore waters. The precipitation of ankerite and siderite is sensitive to the rate of reduction of Fe(III) mineral precursors such as goethite or glauconite. The accumulation of carbonates in the rock matrix leads to a considerable decrease in porosity. This in turn adversely affects permeability and fluid flow in the aquifer. The numerical experiments described here provide useful insight into sequestration mechanisms, and their controlling geochemical conditions and parameters

Geochemistry and origins of mineralized waters in the Floridan aquifer system, northeastern Florida

Science.gov (United States)

Phelps, G.G.

2001-01-01

Increases in chloride concentration have been observed in water from numerous wells tapping the Floridan aquifer system in northeastern Florida. Although most increases have been in the eastern part of Duval County, Florida, no spatial pattern in elevated chloride concentrations is discernible. Possible sources of the mineralized water include modern seawater intrusion; unflushed Miocene-to-Pleistocene-age seawater or connate water in aquifer sediments; or mineralized water from deeper zones of the aquifer system or from formations beneath the Floridan aquifer system. The purpose of this study was to document the chemical and isotopic characteristics of water samples from various aquifer zones, and from geochemical and hydrogeologic data, to infer the source of the increased mineralization. Water samples were collected from 53 wells in northeastern Florida during 1997-1999. Wells tapped various zones of the aquifer including: the Fernandina permeable zone (FPZ), the upper zone of the Lower Floridan aquifer (UZLF), the Upper Floridan aquifer (UFA), and both the UFA and the UZLF. Water samples were analyzed for major ions and trace constituents and for isotopes of carbon, oxygen, hydrogen, sulfur, strontium, chlorine, and boron. Samples of rock from the aquifer were analyzed for isotopes of oxygen, carbon, and strontium. In general, water from various aquifer zones cannot be differentiated based on chemistry, except for water from FPZ wells. Major-ion concentrations vary as much within the upper zone of the Lower Floridan aquifer and the Upper Floridan aquifer as between these two zones. Simple models of mixing between fresh ground water and either modern seawater or water from the FPZ as a mineralized end member show that many water samples from the UZLF aquifer and the UFA are enriched in bicarbonate, calcium, magnesium, sulfate, fluoride, and silica and are depleted in sodium and potassium (as compared to concentrations predicted by simple mixing). Chemical mass

Fate of nine recycled water trace organic contaminants and metal(loid)s during managed aquifer recharge into a anaerobic aquifer: Column studies.

Science.gov (United States)

Patterson, B M; Shackleton, M; Furness, A J; Pearce, J; Descourvieres, C; Linge, K L; Busetti, F; Spadek, T

2010-03-01

Water quality changes associated with the passage of aerobic reverse osmosis (RO) treated recycled water through a deep anaerobic pyritic aquifer system was evaluated in sediment-filled laboratory columns as part of a managed aquifer recharge (MAR) strategy. The fate of nine recycled water trace organic compounds along with potential negative water quality changes such as the release of metal(loid)s were investigated in large-scale columns over a period of 12 months. The anaerobic geochemical conditions provided a suitable environment for denitrification, and rapid (half-life 100 days). High retardation coefficients (R) determined for many of the trace organics (R 13 to 67) would increase aquifer residence time and be beneficial for many of the slow degrading compounds. However, for the trace organics with low R values (1.1-2.6) and slow degradation rates (half-life > 100 days), such as N-nitrosodimethylamine, N-nitrosomorpholine and iohexol, substantial biodegradation during aquifer passage may not occur and additional investigations are required. Only minor transient increases in some metal(loid) concentrations were observed, as a result of either pyrite oxidation, mineral dissolution or pH induced metal desorption, followed by metal re-sorption downgradient in the oxygen depleted zone. Crown Copyright 2009. Published by Elsevier Ltd. All rights reserved.

Arsenic release during managed aquifer recharge (MAR)

Science.gov (United States)

Pichler, T.; Lazareva, O.; Druschel, G.

2013-12-01

The mobilization and addition of geogenic trace metals to groundwater is typically caused by anthropogenic perturbations of the physicochemical conditions in the aquifer. This can add dangerously high levels of toxins to groundwater, thus compromising its use as a source of drinking water. In several regions world-wide, aquifer storage and recovery (ASR), a form of managed aquifer recharge (MAR), faces the problem of arsenic release due to the injection of oxygenated storage water. To better understand this process we coupled geochemical reactive transport modeling to bench-scale leaching experiments to investigate and verify the mobilization of geogenic arsenic (As) under a range of redox conditions from an arsenic-rich pyrite bearing limestone aquifer in Central Florida. Modeling and experimental observations showed similar results and confirmed the following: (1) native groundwater and aquifer matrix, including pyrite, were in chemical equilibrium, thus preventing the release of As due to pyrite dissolution under ambient conditions; (2) mixing of oxygen-rich surface water with oxygen-depleted native groundwater changed the redox conditions and promoted the dissolution of pyrite, and (3) the behavior of As along a flow path was controlled by a complex series of interconnected reactions. This included the oxidative dissolution of pyrite and simultaneous sorption of As onto neo-formed hydrous ferric oxides (HFO), followed by the reductive dissolution of HFO and secondary release of adsorbed As under reducing conditions. Arsenic contamination of drinking water in these systems is thus controlled by the re-equilibration of the system to more reducing conditions rather than a purely oxidative process.

Impact assessment of artificial recharge and geo-chemical characterization of the waters of the slick Tebolba (Eastern Tunisia)

International Nuclear Information System (INIS)

Ferchichi, Hajer

2007-01-01

This study concerned the impact assessment of artificial recharge of a coastal aquifer (Tebolba) from the waters of the dam Nebhana and chemical characterization of its waters. The analysis maps piezometric drawn and salinity at various dates since 1940, the establishment of chronic recharge from the years 1992 to 2006, as well as geochemical study of groundwater in the slick Tebolba have enabled us to reach the many results. This study using a multidisciplinary approach (hydrodynamics and geochemical) seeks an assessment of impacts of recharging the water table in Tebolba from the waters of the dam Nebhana through the history of the qualitative and quantitative water the water and a hydro-geochemical study the current state of the waters of the water. (Author). 45 refs

Long-distance electron transfer by cable bacteria in aquifer sediments

DEFF Research Database (Denmark)

Müller, Hubert; Bosch, Julian; Griebler, Christian

2016-01-01

recycling of sulfate by electron transfer over 1–2-cm distance. Sediments were taken from a hydrocarbon-contaminated aquifer, amended with iron sulfide and saturated with water, leaving the sediment surface exposed to air. Steep geochemical gradients developed in the upper 3 cm, showing a spatial separation...... recently been discovered in marine sediments to couple spatially separated redox half reactions over centimeter scales. Here we provide primary evidence that such sulfur-oxidizing cable bacteria can also be found at oxic–anoxic interfaces in aquifer sediments, where they provide a means for the direct...

Hydrogeochemical impact of CO{sub 2} leakage from geological sequestration on shallow potable aquifers

Energy Technology Data Exchange (ETDEWEB)

Cahill, A.G.

2013-09-15

Over the past 10 years scientists have worked in earnest to understand the potential effects of leakage in order that an informed decision on CCGS implementation can be made. This research can be broadly described as aiming to answer two key questions; how deleterious is leakage of CCGS to groundwater resources? and can it be detected geochemically? Some common hydrochemical development is apparent from the literature however many aspects of hydrogeological and hydrogeochemical impact of leakage into shallow aquifers used in water supply remain unclear. In this Ph.D. study an integrated approach was employed in order to answer the two key questions regarding leakage of CO{sub 2} into shallow aquifers. Consequently a combination of laboratory and field investigations were conducted supported by numerical geochemical modeling in order to identify, constrain and quantify processes controlling groundwater chemistry evolution. The output is 4 journal articles and 3 technical reports. In paper I and technical report I simple batch reactors were employed coupled to comprehensive sediment characterization to determine the likely effects of CO{sub 2} on water chemistry in a range of shallow aquifers. Results showed aquifers can be broadly divided into three types; carbonate dominated, silicate dominated and mixed. Each aquifer type showed distinct water chemistry evolution thus inherent risks vary. These studies also highlighted the complexity of risk assessment and detection caused by the range of formation types potentially overlying storage reservoirs. Investigations described in Papers II, III and technical report II increase applicability to real leakage by observing in situ effects including groundwater flow. A silicate dominated shallow aquifer in Vroegum, western Denmark forms the focus of study upon which a series of investigations were conducted. The main field study involved injection of 1600 kg of gas phase CO{sub 2} into the shallow Vroegum aquifer over 72 days

Assessment of the hydrologic setting and mass transport within Saharan and Arabian Aquifers using GRACE, geochemical, geophysical and subsurface data

Science.gov (United States)

Sultan, M.; Sturchio, N. C.; Ahmed, M.; Saleh, S.; Mohamed, A.; Abuabdullah, M. M.; Emil, M. K.; Bettadpur, S. V.; Save, H.; Fathy, K.; Chouinard, K.

2016-12-01

A better understanding of the hydrologic setting, mass transport, origin, evolution, utilization, sustainability, and paleo-climatic recharge conditions of Saharan and Arabian aquifers was achieved by integrating observation from monthly (04/2002 to 03/2016) Gravity Recovery and Climate Experiment (GRACE)-derived Terrestrial Water Storage (TWS) from multiple GRACE solutions (mascons and spherical harmonic fields) with others from geochemical (solute chemistry), isotopic (O, H, Sr), geochronologic (Chlorine-36, Krypton-81), geophysical (aerogravity and aeromagnetic), and subsurface data. The investigated aquifers are: (1) Nubian Sandstone Aquifer System (NSAS; area: 2×106 km2) in northeast Africa and, (2) Mega Aquifer System (MAS; area: 1.1×106 km2) in Arabia. Our findings indicate the NSAS and MAS were largely recharged in previous wet climatic Pleistocene periods, as evidenced by the groundwater ages (up to 1 million years), yet they receive modest local recharge during interleaving dry periods in areas of relatively high (≥ 20 mm/yr) precipitation. In Sudan and Chad (southern NSAS), the average annual precipitation (AAP) is 95 mm/yr and the recharge is estimated at 3.2 x 109 m3/yr ( 7% of AAP); in the southwest parts of the MAS, the recharge at the foothills of the Red Sea mountains is 1.8 x 109 m3/yr (10% of AAP). Uplifts and/or shear zones orthogonal to groundwater flow impede the south to north flow in the NSAS as evidenced by the large differences in GRACE-derived TWS trends, groundwater ages, and isotopic compositions on either side of the east-west trending Uweinat-Aswan uplift. Similarly west to east groundwater flow in the MAS is impeded and impounded up-gradient from the N-S and/or NW-SE trending basement structures, reactivated during Red Sea opening. Shear zones subparallel to groundwater flow act as preferred flow pathways, as is the case with the NE-SW trending Pelusium shear zone which channels groundwater from the Kufra sub-basin (Libya

The fluoride in the groundwater of Guarani Aquifer System: the origin associated with black shales of Paraná Basin

Science.gov (United States)

Kern, M. L.; Vieiro, A. P.; Machado, G.

2008-09-01

This work presents petrological and geochemical results of the black shales interval from Permian and Devonian strata of the Paraná Basin, Brazil and its relationships with fluoride of groundwater from Guarani Aquifer System. The Guarani Aquifer, located in South Brazil, Uruguay, Paraguay and Argentine, presents contents of fluoride higher than the Brazilian accepted potability limits. Several hypotheses have been presented for the origin of the fluoride in the groundwater of the Guarani Aquifer. Microcrystalline fluorite was registered in black shales of Ponta Grossa and Irati formations from Paraná Basin. The results shown in this work suggest that fluoride present in groundwater of Guarani Aquifer can be originated in deeper groundwater that circulates in Ponta Grossa and Irati formations. The interaction of the groundwater coming from deeper black shales with the groundwater-bearing Aquifer Guarani System occurs through regional fragile structures (faults and fractures) that constitute excellent hydraulic connectors between the two sedimentary packages. The microcrystalline fluorite registered in Ponta Grossa and Irati Formations can be dissolved promoting fluoride enrichment in groundwater of these black shales and Guarani Aquifer System.

Version 4. 00 of the MINTEQ geochemical code

Energy Technology Data Exchange (ETDEWEB)

Eary, L.E.; Jenne, E.A.

1992-09-01

The MINTEQ code is a thermodynamic model that can be used to calculate solution equilibria for geochemical applications. Included in the MINTEQ code are formulations for ionic speciation, ion exchange, adsorption, solubility, redox, gas-phase equilibria, and the dissolution of finite amounts of specified solids. Since the initial development of the MINTEQ geochemical code, a number of undocumented versions of the source code and data files have come into use at the Pacific Northwest Laboratory (PNL). This report documents these changes, describes source code modifications made for the Aquifer Thermal Energy Storage (ATES) program, and provides comprehensive listings of the data files. A version number of 4.00 has been assigned to the MINTEQ source code and the individual data files described in this report.

Version 4.00 of the MINTEQ geochemical code

Energy Technology Data Exchange (ETDEWEB)

Eary, L.E.; Jenne, E.A.

1992-09-01

The MINTEQ code is a thermodynamic model that can be used to calculate solution equilibria for geochemical applications. Included in the MINTEQ code are formulations for ionic speciation, ion exchange, adsorption, solubility, redox, gas-phase equilibria, and the dissolution of finite amounts of specified solids. Since the initial development of the MINTEQ geochemical code, a number of undocumented versions of the source code and data files have come into use at the Pacific Northwest Laboratory (PNL). This report documents these changes, describes source code modifications made for the Aquifer Thermal Energy Storage (ATES) program, and provides comprehensive listings of the data files. A version number of 4.00 has been assigned to the MINTEQ source code and the individual data files described in this report.

Evaluation of the fate of arsenic-contaminated groundwater at different aquifers of Thar coalfield Pakistan.

Science.gov (United States)

Ali, Jamshed; Kazi, Tasneem G; Baig, Jameel A; Afridi, Hassan I; Arain, Mariam S; Ullah, Naeem; Brahman, Kapil D; Arain, Sadaf S; Panhwar, Abdul H

2015-12-01

In present study, the ground water at different aquifers was evaluated for physicochemical parameters, iron, total arsenic, total inorganic arsenic and arsenic species (arsenite and arsenate). The samples of groundwater were collected at different depths, first aquifer (AQ1) 50-60 m, second aquifer (AQ2) 100-120 m, and third aquifer (AQ3) 200-250 m of Thar coalfield, Pakistan. Total inorganic arsenic was determined by solid phase extraction using titanium dioxide as an adsorbent. The arsenite was determined by cloud point extraction using ammonium pyrrolidinedithiocarbamate as a chelating reagent, and resulted complex was extracted by Triton X-114. The resulted data of groundwater were reported in terms of basic statistical parameters, principal component, and cluster analysis. The resulted data indicated that physicochemical parameters of groundwater of different aquifers were exceeded the World Health Organization provisional guideline for drinking water except pH and SO4(2-). The positive correlation was observed between arsenic species and physicochemical parameters of groundwater except F(-) and K(+), which might be caused by geochemical minerals. Results of cluster analysis indicated that groundwater samples of AQ1 was highly contaminated with arsenic species as compared to AQ2 and AQ3 (p > 0.05).

Hydrogeochemical and isotopic investigation and water quality assessment of groundwater in the Sisseb El Alem Nadhour Saouaf aquifer (SANS), northeastern Tunisia

Science.gov (United States)

Hamdi, Mohamed; Zagrarni, Mohamed Faouzi; Jerbi, Hamza; Tarhouni, Jamila

2018-05-01

In the Sisseb El Alem Nadhour Saouaf basin (SANS), as in all other arid regions, surface water is scarce and groundwater is the greatest most important source of water for all uses. This study aims to identify the processes governing groundwater mineralization in order to assess the suitability of the groundwater for drinking and agriculture purposes. This research used a geodatabase which includes information on hydrogeology, geochemistry, land cover, and geology. We identified the most important factors involved in the deterioration of water quality, including anhydrite and gypsum dissolution, silicate weathering, downward leakage between aquifers, evaporation, groundwater over-exploitation, and the overuse of fertilizers. Furthermore, the two following important factors were identified: the intrusion of Sebkhat El Kelbia and the vertical flow from the deep aquifer. Results were used to develop a conceptual geochemical model, wherein three geochemical regions were differentiated. Statistical techniques, such as Principal Component Analysis (PCA) and Hierarchical Cluster Analysis (HCA) were used to confirm the water affinities and the presence of three different geochemical regions. The water quality index (WQI), Wilcox and Richards's diagrams were performed to assess the suitability of groundwater to drinking and irrigation purposes. These indexes confirm the fact that the groundwater of this aquifer is not suitable for irrigation, neither for drinking. Furthermore, 18O and deuterium isotope data indicate the importance of evaporation in the basin, and the recharge with modern rainfall.

Isotope characterization of shallow aquifers in the Horombe region, South of Madagascar

International Nuclear Information System (INIS)

Fareze, L.P.; Rajaobelison, J.; Ramaroson, V.; Raoelina Andriambololona; Andriamiarintsoa, G.; Razafitsalama, P.R.; Rahobisoa, J.J.; Randrianarison, H.; Ranaivoarisoa, A.; Marah, H.

2011-01-01

The present study deals with the problem of evaluation of the recharge mechanism and the characterization of the groundwater flow system in the basement shallow aquifer, which is one of the groundwater resource in the semi-arid South region of Madagascar. Stable isotopes (deuterium and oxygen-18) and tritium are used to achieve with accuracy the hydrogeological and geochemical dynamics study. Chemical analysis is used to provide complementary information to the investigation. A space distribution of tritium concentration and isotopic composition in groundwater shows evidence of two opposite categories of aquifers, which is confirmed by the chemical analysis results and by the geological features of the study site. Some groundwater flow path directions have been identified in the study area thanks to the tritium concentration space distribution and the geological formation. Besides, the groundwater recharge of the shallow aquifers in the South of Madagascar has been characterized by the exponential mixing model.

Isotopes to Study the coastal aquifer plain, Cap Bon, Tunisia

International Nuclear Information System (INIS)

Ben Hamouda, M. F.; Zouari, Kamel; Tarhouni, J.; Gaye, C.B.; Oueslati, M.N.

2005-01-01

The study area is located in the northeastern part of Tunisia about 60 km south of the Tunis city. It is bounded by the Gulf of Haematite in the East, Djebel Sidi Aberahmane in the West, The town of Nabeul in the south and the area of the town Kelibia in the north. The landscape is a coastal plain slightly sloping (3%) towards the sea. The groundwater of the Oriental coast aquifer system occurs mainly at two levels, a shallow aquifer up to depths of about 50 m whose reservoir is consisted by sediments of the Plio quaternary and a deep aquifer between about 150 and 400 m located in the sand stone formations of Miocene of the anticline of Djebel Sidi Abderrahmene. The climate of the region is semi-arid to sub-humid and of Mediterranean type. There are no perennial rivers in this region; but intense storms occasionally cause surface runoff, which is discharged by the oueds. The study is related to a technical cooperation project with the International Atomic Energy Agency, Vienna, Austria, aimed at the use of isotope techniques to study the seawater intrusion into the coastal aquifers of Cap Bon in Tunisia. In this regard, a better understanding of the recharge and flow regime as well as the origin or salinity of the groundwater was required. To reach this goal, isotope and geochemical investigations were carried out. Water samples were taken from wells, boreholes from deep and shallow aquifer of the Oriental coastal aquifer located between Beni Khiar in the south and Kelibia in the north. The samples were analysed for their chemical and isotopic compositions (18O, 2H, 3H, 13C, 14C, 34S). In the following, the results of these analyses are presented and discussed in terms of the recharge and flow regime of the groundwater and the origin and evolution of its salinity. The results of geochemical and isotopic studies have shown that the groundwater is very eterogeneous and suggest the aquifer is replenished by recent water coming from direct infiltration from rain. At

Well-based stable carbon isotope leakage monitoring of an aquifer overlying the CO2 storage reservoir at the Ketzin pilot site, Germany

Science.gov (United States)

Nowak, Martin; Myrttinen, Anssi; Zimmer, Martin; van Geldern, Robert; Barth, Johannes A. C.

2014-05-01

At the pilot site for CO2 storage in Ketzin, a new well-based leakage-monitoring concept was established, comprising geochemical and hydraulic observations of the aquifer directly above the CO2 reservoir (Wiese et al., 2013, Nowak et al. 2013). Its purpose was to allow early detection of un-trapped CO2. Within this monitoring concept, we established a stable carbon isotope monitoring of dissolved inorganic carbon (DIC). If baseline isotope values of aquifer DIC (δ13CDIC) and reservoir CO2 (δ13CCO2) are known and distinct from each other, the δ13CDIC has the potential to serve as an an early indicator for an impact of leaked CO2 on the aquifer brine. The observation well of the overlying aquifer was equipped with an U-tube sampling system that allowed sampling of unaltered brine. The high alkaline drilling mud that was used during well drilling masked δ13CDIC values at the beginning of the monitoring campaign. However, subsequent monitoring allowed observing on-going re-equilibration of the brine, indicated by changing δ13CDIC and other geochemical values, until values ranging around -23 ‰ were reached. The latter were close to baseline values before drilling. Baselineδ13CDIC and δ13CCO2 values were used to derive a geochemical and isotope model that predicts evolution of δ13CDIC, if CO2 from the reservoir would leak into the aquifer. The model shows that equilibrium isotope fractionation would have to be considered if CO2 dissolves in the brine. The model suggests that stable carbon isotope monitoring is a suitable tool to assess the impact of injected CO2 in overlying groundwater aquifers. However, more data are required to close gaps of knowledge about fractionation behaviour within the CO2(g) - DIC system under elevated pressures and temperatures. Nowak, M., Myrttinen, A., Zimmer, M., Wiese, B., van Geldern, R., Barth, J.A.C., 2013. Well-based, Geochemical Leakage Monitoring of an Aquifer Immediately Above a CO2 Storage Reservoir by Stable Carbon

The chemical behavior of the transuranic elements and the barrier function in natural aquifer systems

International Nuclear Information System (INIS)

Jewett, J.R.

1997-01-01

In a geological repository for long-lived radioactive wastes, such as actinides and certain fission products, most of the stored radionuclides remain immobile in the particular geological formation. If any of these could possibly become mobile, only trace concentrations of a few radionuclides would result. Nevertheless, with an inventory in the repository of many tonnes of transuranic elements, the amounts that could disperse cannot be neglected. A critical assessment of the chemical behavior of these nuclides, especially their migration properties in the aquifer system around the repository site, is mandatory for analysis of the long-term safety. The chemistry requited for this includes many geochemical multicomponent reactions that are so far only partially understood and hich therefore can be quantified only incompletely. A few of these reactions have been discussed in this paper based on present knowledge. If a comprehensive discussion of the subject is impossible because of this ack of information then an attempt to emphasize the importance of the predominant geochemical reactions of the transuranic elements in various aquifer systems should be made

Bacterial community and groundwater quality changes in an anaerobic aquifer during groundwater recharge with aerobic recycled water.

Science.gov (United States)

Ginige, Maneesha P; Kaksonen, Anna H; Morris, Christina; Shackelton, Mark; Patterson, Bradley M

2013-09-01

Managed aquifer recharge offers the opportunity to manage groundwater resources by storing water in aquifers when in surplus and thus increase the amount of groundwater available for abstraction during high demand. The Water Corporation of Western Australia (WA) is undertaking a Groundwater Replenishment Trial to evaluate the effects of recharging aerobic recycled water (secondary treated wastewater subjected to ultrafiltration, reverse osmosis, and ultraviolet disinfection) into the anaerobic Leederville aquifer in Perth, WA. Using culture-independent methods, this study showed the presence of Actinobacteria, Alphaproteobacteria, Bacilli, Betaproteobacteria, Cytophaga, Flavobacteria, Gammaproteobacteria, and Sphingobacteria, and a decrease in microbial diversity with an increase in depth of aquifer. Assessment of physico-chemical and microbiological properties of groundwater before and after recharge revealed that recharging the aquifer with aerobic recycled water resulted in elevated redox potentials in the aquifer and increased bacterial numbers, but reduced microbial diversity. The increase in bacterial numbers and reduced microbial diversity in groundwater could be a reflection of an increased denitrifier and sulfur-oxidizing populations in the aquifer, as a result of the increased availability of nitrate, oxygen, and residual organic matter. This is consistent with the geochemical data that showed pyrite oxidation and denitrification within the aquifer after recycled water recharge commenced. © 2013 Federation of European Microbiological Societies. Published by John Wiley & Sons Ltd. All rights reserved.

Geochemical and stable isotopic evolution of the Guarani Aquifer System in the state of São Paulo, Brazil

Science.gov (United States)

Sracek, Ondra; Hirata, Ricardo

2002-09-01

The purpose of this report is to explain geochemical and stable isotopes trends in the Brazilian unit of the Guarani Aquifer System (Botucatu and Piramboia aquifers) in São Paulo State, Brazil. Trends of dissolved species concentrations and geochemical modeling indicated a significant role of cation exchange and dissolution of carbonates in downgradient evolution of groundwater chemistry. Loss of calcium by the exchange for sodium drives dissolution of carbonates and results in Na-HCO3 type of groundwater. The cation-exchange front moves downgradient at probably much slower rate compared to the velocity of groundwater flow and at present is located near to the cities of Sertãozinho and Águas de Santa Barbara (wells PZ-34 and PZ-148, respectively) in a shallow confined area, 50-70 km from the recharge zone. Part of the sodium probably enters the Guarani Aquifer System. together with chloride and sulfate from the underlying Piramboia Formation by diffusion related to the dissolution of evaporates like halite and gypsum. High concentrations of fluorine (up to 13.3 mg/L) can be explained by dissolution of mineral fluoride also driven by cation exchange. However, it is unclear if the dissolution takes place directly in the Guarani Aquifer System or in the overlying basaltic Serra Geral Formation. There is depletion in δ2H and δ18O values in groundwater downgradient. Values of δ13C(DIC) are enriched downgradient, indicating dissolution of calcite under closed system conditions. Values of δ13C(DIC) in deep geothermal wells are very high (>-6.0‰) and probably indicate isotopic exchange with carbonates with δ13C about -3.0‰. Future work should be based on evaluation of vertical fluxes and potential for penetration of contamination to the Guarani Aquifer System. Résumé. Cet article a pour objet d'expliquer l'évolution de la géochimie et des isotopes stables dans l'unité brésilienne du système aquifère du Guarani (aquifères de Botucatu et Piramboia), dans

Geochemical Fractionations and Mobility of Arsenic, Lead and Cadmium in Sediments of the Kanto Plain, Japan.

Science.gov (United States)

Hossain, Sushmita; Oguchi, Chiaki T.; Hachinohe, Shoichi; Ishiyama, Takashi; Hamamoto, Hideki

2014-05-01

Lowland alluvial and floodplain sediment play a major role in transferring heavy metals and other elements to groundwater through sediment water interaction in changing environmental conditions. However identification of geochemical forms of toxic elements such as arsenic (As), lead (Pb) and cadmium (Cd) requires risk assessment of sediment and subsequent groundwater pollution. A four steps sequential extraction procedure was applied to characterize the geochemical fractionations of As, Pb and Cd for 44 sediment samples including one peat sample from middle basin area of the Nakagawa river in the central Kanto plain. The studied sediment profile extended from the bottom of the river to 44 m depth; sediment samples were collected at 1m intervals from a bored core. The existing sedimentary facies in vertical profile are continental, transitional and marine. There are two aquifers in vertical profile; the upper aquifer (15-20m) contains fine to medium sand whereas medium to coarse sand and gravelly sand contain in lower aquifer (37-44m). The total As and Pb contents were measured by the X-Ray Fluorescence analysis which ranged from 4 to 23 mg/kg of As and 10 to 27 mg/kg of Pb in sediment profile. The three trace elements and major heavy metals were determined by ICP/MS and ICP/AES, and major ions were measured by an ion chromatograph. The marine sediment is mainly Ca-SO4 type. The Geochemical analysis showed the order of mobility trends to be As > Pb > Cd for all the steps. The geochemical fractionations order was determined to be Fe-Mn oxide bound > carbonate bound > ion exchangeable > water soluble for As and Pb whereas the order for Cd is carbonate bound > Fe-Mn oxide bound > ion exchangeable > water soluble. The mobility tendency of Pb and Cd showed high in fine silty sediment of marine environment than for those from continental and transitional environments. In the case of As, the potential mobility is very high (>60%) in the riverbed sediments and clayey silt

Hydro-geochemical characterization of Treated Domestic Waste Water for possible use in homestead irrigation and managed aquifer recharge in the coastal city of Khulna, Bangladesh

Science.gov (United States)

Hamid, T.; Ahmed, K. M.

2016-12-01

Bangladesh is among the most densely populated countries in the world. Rapid and unplanned urbanization in Bangladesh has resulted in heterogeneous land use pattern and larger demands for municipal water. To meet the ever-increasing demand of water for such population, the usage of treated domestic waste water (DWW) has become a viable option that can serve specific purposes, i.e. homestead irrigation, managed aquifer recharge (MAR) in major cities like Khulna, the largest city in the southwest coastal region. It is an attractive solution to minimize the deficit between the demand and supply of water in the study area where, in specific parts, city-dwellers suffer year round shortage of potable water due to high salinity in shallow depths. However, certain degree of treatment is mandatory for DWW in order to ensure the compliance of the output water with a set of standards and regulations for the DWW reuse. At present, the DWW is being treated through Constructed Wetlands but the treated water is not used and discharged into the sewer system. Wastewater that has been treated through a constructed wetland is a resource that can be used for productive uses in homestead garden irrigation, artificial aquifer recharge, and other non-potable uses. The study addresses the effectiveness of constructed wetlands in improving the quality of wastewater through on the hydro-geochemical characterization of both raw and treated DWW as well as baseline water quality analysis of surface and ground water in and around the treatment plant with consideration of seasonal variations. The study aims at sustainable development through conservation of water, satisfaction of demands, reliability of water supply, contribution to urban food supply, sustenance of livelihood and replenishment of the depleting aquifer by assessing the suitability of the treated DWW for various non-potable uses and also to provide guidelines for possible uses of treated DWW without adverse impact on environment

An overview of nitrate sources and operating processes in arid and semiarid aquifer systems.

Science.gov (United States)

Gutiérrez, Mélida; Biagioni, Richard N; Alarcón-Herrera, Maria Teresa; Rivas-Lucero, Bertha A

2018-05-15

Nitrate concentration in most aquifers in arid and semi-arid areas has increased in the past several decades as a result of human activities. Under the predominantly oxic conditions of these aquifers, denitrification is inhibited, allowing nitrate, a soluble and stable form of nitrogen (N), to accumulate. Because of its close association with municipal and agricultural wastes, nitrate is commonly used as an indicator of anthropogenic contamination. Aquifers affected by agricultural waste may contain salts from irrigation returns and herbicides in addition to nitrates. Preventing leakage from soil to deeper parts of the aquifer is thus a priority in the sustainable management of aquifers in arid and semiarid areas. Studies report a wide range of nitrate concentrations distributed non-uniformly within the aquifer, with roughly 40% and 20% of sampled wells exceeding 50mg/L nitrate in shallow and deep parts of the aquifer respectively. In aquifers at risk of becoming contaminated, nitrate isotopes (δ 15 N, δ 18 O, Δ 17 O) can be used to identify the source of nitrogen as mineral or organic fertilizer, sewage, or atmospheric deposition. A variety of mathematical models (crop, hydrological, geochemical, or a combination of them) have been successful in identifying best practices that minimize N leakage without negatively affecting crop yield. In addition, field research in crop management, e.g., conservation agriculture, has yielded promising results in determining the adequate dosage and time of application of fertilizers to reduce N losses. Examples of key dryland aquifers impacted by nitrate are discussed, and some of the most pressing challenges to achieve sustainability are presented. Copyright © 2017 Elsevier B.V. All rights reserved.

Using geochemical indicators to distinguish high biogeochemical activity in floodplain soils and sediments

Energy Technology Data Exchange (ETDEWEB)

Kenwell, Amy [Hydrologic Sciences and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Navarre-Sitchler, Alexis, E-mail: asitchle@mines.edu [Hydrologic Sciences and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Prugue, Rodrigo [Hydrologic Sciences and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Spear, John R. [Department of Civil and Environmental Engineering, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Hering, Amanda S. [Department of Applied Mathematics and Statistics, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Maxwell, Reed M. [Hydrologic Sciences and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Carroll, Rosemary W.H. [Desert Research Institute, Division of Hydrologic Sciences, 2215 Raggio Parkway, Reno, NV 89512 (United States); Williams, Kenneth H. [Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States)

2016-09-01

A better understanding of how microbial communities interact with their surroundings in physically and chemically heterogeneous subsurface environments will lead to improved quantification of biogeochemical reactions and associated nutrient cycling. This study develops a methodology to predict potential elevated rates of biogeochemical activity (microbial “hotspots”) in subsurface environments by correlating microbial DNA and aspects of the community structure with the spatial distribution of geochemical indicators in subsurface sediments. Multiple linear regression models of simulated precipitation leachate, HCl and hydroxylamine extractable iron and manganese, total organic carbon (TOC), and microbial community structure were used to identify sample characteristics indicative of biogeochemical hotspots within fluvially-derived aquifer sediments and overlying soils. The method has been applied to (a) alluvial materials collected at a former uranium mill site near Rifle, Colorado and (b) relatively undisturbed floodplain deposits (soils and sediments) collected along the East River near Crested Butte, Colorado. At Rifle, 16 alluvial samples were taken from 8 sediment cores, and at the East River, 46 soil/sediment samples were collected across and perpendicular to 3 active meanders and an oxbow meander. Regression models using TOC and TOC combined with extractable iron and manganese results were determined to be the best fitting statistical models of microbial DNA (via 16S rRNA gene analysis). Fitting these models to observations in both contaminated and natural floodplain deposits, and their associated alluvial aquifers, demonstrates the broad applicability of the geochemical indicator based approach. - Highlights: • Biogeochemical characterization of alluvial floodplain soils and sediments was performed to investigate parameters that may indicate microbial hot spot formation. • A correlation between geochemical parameters (total organic carbon and

Using geochemical indicators to distinguish high biogeochemical activity in floodplain soils and sediments

International Nuclear Information System (INIS)

Kenwell, Amy; Navarre-Sitchler, Alexis; Prugue, Rodrigo; Spear, John R.; Hering, Amanda S.; Maxwell, Reed M.; Carroll, Rosemary W.H.; Williams, Kenneth H.

2016-01-01

A better understanding of how microbial communities interact with their surroundings in physically and chemically heterogeneous subsurface environments will lead to improved quantification of biogeochemical reactions and associated nutrient cycling. This study develops a methodology to predict potential elevated rates of biogeochemical activity (microbial “hotspots”) in subsurface environments by correlating microbial DNA and aspects of the community structure with the spatial distribution of geochemical indicators in subsurface sediments. Multiple linear regression models of simulated precipitation leachate, HCl and hydroxylamine extractable iron and manganese, total organic carbon (TOC), and microbial community structure were used to identify sample characteristics indicative of biogeochemical hotspots within fluvially-derived aquifer sediments and overlying soils. The method has been applied to (a) alluvial materials collected at a former uranium mill site near Rifle, Colorado and (b) relatively undisturbed floodplain deposits (soils and sediments) collected along the East River near Crested Butte, Colorado. At Rifle, 16 alluvial samples were taken from 8 sediment cores, and at the East River, 46 soil/sediment samples were collected across and perpendicular to 3 active meanders and an oxbow meander. Regression models using TOC and TOC combined with extractable iron and manganese results were determined to be the best fitting statistical models of microbial DNA (via 16S rRNA gene analysis). Fitting these models to observations in both contaminated and natural floodplain deposits, and their associated alluvial aquifers, demonstrates the broad applicability of the geochemical indicator based approach. - Highlights: • Biogeochemical characterization of alluvial floodplain soils and sediments was performed to investigate parameters that may indicate microbial hot spot formation. • A correlation between geochemical parameters (total organic carbon and

Use of a time-domain electromagnetic method with geochemical tracers to explore the salinity anomalies in a small coastal aquifer in north-eastern Tunisia

Science.gov (United States)

Chekirbane, Anis; Tsujimura, Maki; Kawachi, Atsushi; Lachaal, Fethi; Isoda, Hiroko; Tarhouni, Jamila

2014-12-01

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

A conceptual model for groundwater flow and geochemical evolution in the southern Outaouais Region, Québec, Canada

International Nuclear Information System (INIS)

Montcoudiol, N.; Molson, J.; Lemieux, J.-M.; Cloutier, V.

2015-01-01

Highlights: • Geochemical and isotope data help constrain the 2D conceptual flow model. • Stable isotopes indicate recharge occurring under conditions similar to current climate. • Mixing was found between younger ( 3 H) and older ( 14 C and 4 He) groundwater. • Mixing occurred under natural flow conditions and/or was induced during sampling. • The new conceptual model shows dominant local and intermediate flow systems. - Abstract: A conceptual model was developed for a hydrogeological flow system in the southern Outaouais Region, Quebec, Canada, where the local population relies heavily on groundwater pumped from shallow overburden aquifers and from deeper fractured crystalline bedrock. The model is based on the interpretation of aqueous inorganic geochemical data from 14 wells along a cross-section following the general flow direction, of which 9 were also analysed for isotopes (δ 18 O, δ 2 H, 3 H, δ 13 C, 14 C) and 4 for noble gases (He, Ne, Ar, Xe, Kr). Three major water types were identified: (1) Ca–HCO 3 in the unconfined aquifer as a result of silicate (Ca-feldspar) weathering, (2) Na–Cl as a remnant of the post-glacial Champlain Sea in stagnant confined zones of the aquifer, and (3) Na–HCO 3 , resulting from freshening of the confined aquifer due to Ca–Na cation exchange. Chemical data also allowed the identification of significant mixing zones. Isotope and noble gas data confirm the hypothesis of remnant water from the Champlain Sea and also support the hypothesis of mixing processes between a young tritium-rich component with an older component containing high 4 He concentrations. It is still unclear if the mixing occurs under natural flow conditions or if it is induced by pumping during the sampling, most wells being open boreholes in the bedrock. It is clear, however, that the hydrogeochemical system is dynamic and still evolving from induced changes since the last glaciation. As a next step, the conceptual model will serve as a

Geochemical and hydrologic controls on the mobilization of arsenic derived from herbicide application

International Nuclear Information System (INIS)

Fitzmaurice, Arthur G.; Bilgin, A. Azra; O'Day, Peggy A.; Illera, Virginia; Burris, David R.; Reisinger, H. James; Hering, Janet G.

2009-01-01

The fate and transport of As was examined at an industrial site where soil- and groundwater contamination are derived from the application of As 2 O 3 as a herbicide. Application of arsenical herbicides was discontinued in the 1970s and soils in the source area were partially excavated in 2003. Arsenic contamination (up to 280 mg/kg) remains in the source area soils and a plume of As-contaminated groundwater persists in the surficial aquifer downgradient of the source area with maximum observed As concentrations of 1200 μg/L near the source area. The spatial extent of As contamination as defined by the 10 μg/L contour appears to have remained relatively stable over the period 1996-2006; the boundary of the 1000 μg/L contour has retreated over the same time period indicating a decrease in total As mass in the surficial groundwater. In column experiments conducted with source area soil, the As concentrations in the column effluent were comparable to those observed in groundwater near the source area. A substantial fraction of the As could be leached from the source area soil with ammonium sulfate and ammonium phosphate. Exhaustive extraction with background groundwater removed most of the total As. These results indicate that As in the source area soils is geochemically labile. Source area soils are low in extractable Fe, Mn and Al, and characterization by X-ray absorption spectroscopy and electron microscopy indicated that As is present primarily as arsenate sorbed to (alumino)silicate minerals. Batch sorption experiments showed much less sorption on surficial aquifer sediments than on sediments from the Jackson Bluff Formation (JBF), a presumed confining layer. This limited capacity of the surficial aquifer sediments for As sorption is consistent with the similar As contents observed for these sediments within and upgradient of the As plume. The apparent stability of the As plume cannot be explained by sequestration of As within the surficial aquifer. Sorption

Relationship between tectonic structures and hydrogeochemical compartmentalization in aquifers: Example of the “Jeffara de Medenine” system, south–east Tunisia

Directory of Open Access Journals (Sweden)

Hayet Chihi

2015-09-01

The kriged maps of major-ion concentrations and of total dissolved solids in the aquifers were then analyzed and compared with the reservoir facies distribution for each compartment, the geometric characteristics of the aquifer, and the piezometric level trends. This allowed to characterize the hydraulic behavior of the Medenine fault and to understand the underlying physical and chemical processes having led to the spatial distribution of the geochemical properties, and thus, the hydrogeochemical functioning of the aquifers.

Some results of NURE uranium geochemical studies

International Nuclear Information System (INIS)

Price, V. Jr.

1979-01-01

Some technical developments of the National Uranium Resource Evaluation Program which are of general application in geochemical exploration are being studied. Results of stream water and suspended and bottom sediment analyses are compared for an area near Williamsport, Pennsylvania. Variations of uranium content of water samples with time in the North Carolina Piedmont are seen to correlate with rainfall. Ground water samples from coastal and piedmont areas were analyzed for helium. All media sampled provide useful information when properly analyzed and interpreted as part of a total geological analysis of an area

Geochemical and isotopic characterization of the ground water of Oued Laya

International Nuclear Information System (INIS)

Hkiri, Sabrine

2010-01-01

In the Sahel region of Sousse (Tunisia Center East), almost all of the deep groundwater has undergone over the last decade, a general decline of groundwater level. This decrease is caused by two factors, the intensive farming and drought. These aquifers, despite their often poor quality (high salinity), are increasingly used, so they are now home to intense exploitation, whose consequences have emerged as significant declines of groundwater level and degradation of the chemical quality of their water. This study concerns a groundwater aquifer that is under stress and anthropogenic climate severe enough: the coastal aquifer of Wad Laya present quality of groundwater qualified low salinity point of view compared to other neighboring aquifers. The salinity is apparently not related to over exploitation as the majority of coastal aquifers but seems it is due to the geological nature which forms the water table. The region's climate is semiarid with an average annual rainfall of 320 mm by 100 years; the FTE is 1750 mm / year resulting in a water deficit of more than 1.4 m / year. Renewable resources are estimated at 3.3 million m3, while for the levy is estimated to be 2.7 million m3 which the dry residue is currently spent 5g / l (CRDA Sousse, 2009). The objective of this study included hydrogeological characterization of the aquifer using geophysical tools and identification of mechanisms of salination using geochemical and isotopic tools to determine the possible origins of mineralization. For this campaign sampling and measurement was made in the region over a thirty water points in order to measure the electrical conductivity, groundwater level and analyze the chemical composition (major and trace elements). Initial findings from this study are summarized in: Completion of piezometric maps and potentiometric study of the evolution in some wells show a decline of water table caused by the increased exploitation and lower rainfall, which resulted in an increase in

Quality of groundwater at and near an aquifer storage and recovery site, Bexar, Atascosa, and Wilson Counties, Texas, June 2004-August 2008

Science.gov (United States)

Otero, Cassi L.; Petri, Brian L.

2010-01-01

The U.S. Geological Survey, in cooperation with the San Antonio Water System, did a study during 2004-08 to characterize the quality of native groundwater from the Edwards aquifer and pre- and post-injection water from the Carrizo aquifer at and near an aquifer storage and recovery (ASR) site in Bexar, Atascosa, and Wilson Counties, Texas. Groundwater samples were collected and analyzed for selected physical properties and constituents to characterize the quality of native groundwater from the Edwards aquifer and pre- and post-injection water from the Carrizo aquifer at and near the ASR site. Geochemical and isotope data indicated no substantial changes in major-ion, trace-element, and isotope chemistry occurred as the water from the Edwards aquifer was transferred through a 38-mile pipeline to the aquifer storage and recovery site. The samples collected from the four ASR recovery wells were similar in major-ion and stable isotope chemistry compared to the samples collected from the Edwards aquifer source wells and the ASR injection well. The similarity could indicate that as Edwards aquifer water was injected, it displaced native Carrizo aquifer water, or, alternatively, if mixing of Edwards and Carrizo aquifer waters was occurring, the major-ion and stable isotope signatures for the Carrizo aquifer water might have been obscured by the signatures of the injected Edwards aquifer water. Differences in the dissolved iron and dissolved manganese concentrations indicate that either minor amounts of mixing occurred between the waters from the two aquifers, or as Edwards aquifer water displaced Carrizo aquifer water it dissolved the iron and manganese directly from the Carrizo Sand. Concentrations of radium-226 in the samples collected at the ASR recovery wells were smaller than the concentrations in samples collected from the Edwards aquifer source wells and from the ASR injection well. The smaller radium-226 concentrations in the samples collected from the ASR

Status report on geochemical field results from Atlantic study sites

International Nuclear Information System (INIS)

Wilson, T.R.S.; Thomson, J.; Hydes, D.J.; Colley, S.

1983-01-01

This report summarises the results of preliminary geochemical investigations at three North Atlantic study areas. The two eastern sites, on the Cape Verde abyssal plain (CV2) and east of Great Meteor Seamount (GME) were visited during 1982. The results presented are preliminary. Studies in the western Atlantic, close to the Nares Abyssal Plain study site are more detailed and are presented in a separate paper. The report shows for the first time the relative redox status of the three sites. The differences are unexpectedly large, the most reduced cores being recovered at GME and the most oxidised at CV2. The sporadic nature of Recent sediment accumulation at these sites is also emphasised. In order to place these preliminary results in context their relevance to the production of mathematical system models is discussed in a closing section. The necessity for such models to rest on sound foundations of geochemical understanding is noted. Suggestions on future research priorities are offered for discussion. (author)

Using hydrochemical data and modelling to enhance the knowledge of groundwater flow and quality in an alluvial aquifer of Zagreb, Croatia

Energy Technology Data Exchange (ETDEWEB)

Marković, Tamara, E-mail: tmarkovic@hgi-cgs.hr; Brkić, Željka; Larva, Ozren

2013-08-01

The Zagreb alluvial aquifer system is located in the southwest of the Pannonian Basin in the Sava Valley in Croatia. It is composed of Quaternary unconsolidated deposits and is highly utilised, primarily as a water supply for the more than one million inhabitants of the capital city of Croatia. To determine the origin and dynamics of the groundwater and to enhance the knowledge of groundwater flow and the interactions between the groundwater and surface water, extensive hydrogeological and hydrochemical investigations have been completed. The groundwater levels monitored in nested observation wells and the lithological profile indicate that the aquifer is a single hydrogeologic unit, but the geochemical characteristics of the aquifer indicate stratification. The weathering of carbonate and silicate minerals has an important role in groundwater chemistry, especially in the area where old meanders of the Sava River existed. Groundwater quality was observed to be better in the deeper parts of the aquifer than in the shallower parts. Furthermore, deterioration of the groundwater quality was observed in the area under the influence of the landfill. The stable isotopic composition of all sampled waters indicates meteoric origin. NETPATH-WIN was used to calculate the mixing proportions between initial waters (water from the Sava River and groundwater from “regional” flow) in the final water (groundwater sampled from observation wells). According to the results, the mixing proportions of “regional” flow and the river water depend on hydrological conditions, the duration of certain hydrological conditions and the vicinity of the Sava River. Moreover, although the aquifer system behaves as a single hydrogeologic unit from a hydraulic point of view, it still clearly demonstrates geochemical stratification, which could be a decisive factor in future utilisation strategies for the aquifer system. - Highlights: • The Zagreb aquifer is the largest utilised source of

Equilibrium geochemical modeling of a seasonal thermal energy storage aquifer field test

Science.gov (United States)

Stottlemyre, J. S.

1980-01-01

A geochemical mathematical modeling study designed to investigate the well plugging problems encountered at the Auburn University experimental field tests is summarized. The results, primarily of qualitative interest, include: (1) loss of injectivity was probably due to a combination of native particulate plugging and clay swelling and dispersion; (2) fluid-fluid incompatibilities, hydrothermal reactions, and oxidation reactions were of insignificant magnitude or too slow to have contributed markedly to the plugging; and (3) the potential for and contributions from temperature-induced dissolved gas solubility reductions, capillary boundary layer viscosity increases, and microstructural deformation cannot be deconvolved from the available data.

Review of simulation techniques for aquifer thermal energy storage (ATES)

Energy Technology Data Exchange (ETDEWEB)

Mercer, J.W.; Faust, C.R.; Miller, W.J.; Pearson, F.J. Jr.

1981-03-01

The storage of thermal energy in aquifers has recently received considerable attention as a means to conserve and more efficiently use energy supplies. The analysis of aquifer thermal energy storage (ATES) systems will rely on the results from mathematical and geochemical models. Therefore, the state-of-the-art models relevant to ATES was reviewed and evaluated. These models describe important processes active in ATES including ground-water flow, heat transport (heat flow), solute transport (movement of contaminants), and geochemical reactions. In general, available models of the saturated ground-water environment are adequate to address most concerns associated with ATES; that is, design, operation, and environmental assessment. In those cases where models are not adequate, development should be preceded by efforts to identify significant physical phenomena and relate model parameters to measurable quantities. Model development can then proceed with the expectation of an adequate data base existing for the model's eventual use. Review of model applications to ATES shows that the major emphasis has been on generic sensitivity analysis and site characterization. Assuming that models are applied appropriately, the primary limitation on model calculations is the data base used to construct the model. Numerical transport models are limited by the uncertainty of subsurface data and the lack of long-term historical data for calibration. Geochemical models are limited by the lack of thermodynamic data for the temperature ranges applicable to ATES. Model applications undertaken with data collection activities on ATES sites should provide the most important contributions to the understanding and utilization of ATES. Therefore, the primary conclusion of this review is that model application to field sites in conjunction with data collection activities is essential to the development of this technology.

Evaluation of mercury and physicochemical parameters in different depths of aquifer water of Thar coalfield, Pakistan.

Science.gov (United States)

Ali, Jamshed; Kazi, Tasneem G; Tuzen, Mustafa; Ullah, Naeem

2017-07-01

In the current study, mercury (Hg) and physicochemical parameters have been evaluated in aquifer water at different depths of Thar coal field. The water samples were collected from first aquifer (AQ 1 ), second aquifer (AQ 2 ), and third aquifer (AQ 3 ) at three depths, 50-60, 100-120, and 200-250 m, respectively. The results of aquifer water of three depths were interpreted by using different multivariate statistical techniques. Validation of desired method was checked by spiking standard addition method in studied aquifer water samples. The content of Hg in aquifer water samples was measured by cold vapor atomic absorption spectrometer (CV-AAS). These determined values illustrate that the levels of Hg were higher than WHO recommended values for drinking water. All physicochemical parameters were higher than WHO permissible limits for drinking water except pH and SO 4 2- in aquifer water. The positive correlation of Hg with other metals in aquifer water samples of AQ 1 , AQ 2 , and AQ 3 of Thar coalfield except HCO 3 - was observed which might be caused by geochemical minerals. The interpretation of determined values by the cluster technique point out the variations within the water quality parameter as well as sampling location of studied field. The aquifer water AQ 2 was more contaminated with Hg as compared to AQ 1 and AQ 3 ; it may be due to leaching of Hg from coal zone. The concentration of Hg in aquifer water obtained from different depths was found in the following decreasing order: AQ 2  < AQ 1  < AQ 3 .

Arsenic in groundwater of the Red River floodplain, Vietnam: Controlling geochemical processes and reactive transport modeling

DEFF Research Database (Denmark)

Postma, Diederik Jan; Larsen, Flemming; Hue, N.T.M.

2007-01-01

The mobilization of arsenic (As) to the groundwater was studied in a shallow Holocene aquifer on the Red River flood plain near Hanoi, Vietnam. The groundwater chemistry was investigated in a transect of 100 piezometers. Results show an anoxic aquifer featuring organic carbon decomposition......(III) but some As(V) is always found. Arsenic correlates well with NH4, relating its release to organic matter decomposition and the source of As appears to be the Fe-oxides being reduced. Part of the produced Fe(II) is apparently reprecipitated as siderite containing less As. Results from sediment extraction...... chemistry over depth is homogeneous and a reactive transport model was constructed to quantify the geochemical processes along the vertical groundwater flow component. A redox zonation model was constructed using the partial equilibrium approach with organic carbon degradation in the sediment as the only...

Results of a hydrogeological and hydrogeochemical study of a semi-arid karst aquifer in Tezbent plateau, Tebessa region, northeast of Algeria

Science.gov (United States)

Belfar, Dalila; Fehdi, Chemseddine; Baali, Fethi; Salameh, Elias

2017-06-01

The Hammamet Plain, situated in the northwest of the Tezbent mountain range, northeast of Algeria, drains carbonate aquifers through some important karst springs. The physical and chemical characteristics of spring and well water samples were studied for 2 years to assess the origin of groundwater and determine the factors driving the geochemical composition. The ionic speciation and mineral dissolution/precipitation was calculated. Water wells, characterizing groundwater circulation at shallow depths, are moderate to high mineralized waters of Na-HCO3 type. In contrast to the shallow environment, the CO2-rich, deeper waters are of the Ca-HCO3-SO4 type and undergo significant changes in the baseline chemistry along flow lines with increasing residence time. The main factors controlling the groundwater composition and its seasonal variations are the geology, because of the presence of carbonate formations, the elevation and the rate of karst development. In both groups, the carbonate chemistry is diagnostic of the effect of karst development. The supersaturation with respect to calcite indicates CO2 degassing, occurring either inside the aquifer in open conduits, or at the outlet in reservoirs. The undersaturation with respect to calcite shows the existence of fast flow and short residence time conditions inside the aquifer. Interaction between groundwater and surrounding host rocks is believed to be the main process responsible for the observed chemical characteristics of groundwater in the study area.

Origin of water salinity in the coastal Sarafand aquifer (South-Lebanon)

International Nuclear Information System (INIS)

Hashash, Adnan; Aranyossy, J.F.

1996-01-01

Author.The geochemical and isotopic study, based on the analysis of twenty water samples from well in the coastal plain of Sarafand (South-Lebanon), permit to eliminate the hypothesis of marine intrusion in this aquifer. The increase of salinity observed in certain wells is due to the contamination of cretaceous aquifer water by the quaternary formations. The two poles of mixing are respectively characterized: by weak tritium contents (between 2 and 3 UT) and a value of stable isotopes (-5,9<0,18<-5,5) corresponding to the appearance of cretaceous formation area; by the high tritium contents and enrichment relative to heavy isotope in the mineralized water of superficial formations. On the other hand, the isotope contents permit the set a rapid renewal of the cretaceous aquifer water due to quick circulation in the Karstic system

Baseline geochemical characterisation of a vulnerable tropical karstic aquifer; Lifou, New Caledonia

Directory of Open Access Journals (Sweden)

Eric Nicolini

2016-03-01

Full Text Available Study region: Lifou Island, near the main island of New Caledonia. Study focus: Stable oxygen and hydrogen isotopes of groundwater and rainfall were used to characterise baseline values for the main fresh water aquifer of Lifou Island and describe its recharge. Other stable isotope parameters (nitrates and DIC were used to investigate the interaction between surface water (rainfall and groundwater, including anthropogenic effects from human activities. New hydrological insights for the region: This study represents the first baseline isotopic characterisation of Lifou Island’s groundwater aquifer composition and provides a reference for future investigative studies on groundwater quality and security. Groundwater sampled in June and October 2012 had nearly identical isotopic composition. Tap water sampled monthly between February 2012 and January 2014 also had a constant isotopic composition similar to the groundwater. Groundwater recharge was found to occur when monthly precipitation exceeded 140 mm, with the recharge cycle representing 20–30% of the annual rainfall. Relationships between HCO32− content, pH, soil δ13C DIC and satellite photo interpretation suggests a variance of soil pCO2, which is explained by different vegetation cover and higher water use efficiencies in forested areas (high pCO2, more negative δ13C isotope values. The δ15NNO3 values for most groundwater indicate they are uncontaminated with anthropogenic nitrates, although some samples taken in October (dry season showed a slight denitrification, possibly of natural origin. Keywords: Reef islands, Precipitation, Karstic aquifer, Hydrogeology, Stable isotopes, Nitrates

Geophysics- and geochemistry-based assessment of the geochemical characteristics and groundwater-flow system of the U.S. part of the Mesilla Basin/Conejos-Médanos aquifer system in Doña Ana County, New Mexico, and El Paso County, Texas, 2010–12

Science.gov (United States)

Teeple, Andrew P.

2017-06-16

(reported but not used in the assessment), and environmental tracers. The data obtained from these samples (with the exception of the pesticide data) were used to gain insights into processes controlling the groundwater movement through the groundwater system in the study area. Results from the geophysical and geochemical assessments facilitated the interpretation of the geochemical characteristics of the groundwater sources and geochemical groups within the groundwater system.The groundwater-flow system in the study area consists primarily of the Mesilla Basin aquifer system, which can be divided into four hydrogeologic units by using an informal classification scheme based on basin-fill stratigraphy and sedimentology with an emphasis on aquifer characteristics. The four hydrogeologic units are (1) the Rio Grande alluvium, which is the shallow aquifer of the Mesilla Basin within the confines of the Mesilla Valley, and the three hydrogeologic units that compose the Santa Fe Group: (2) the lower part of the Santa Fe Group, which is the least productive zone, (3) the middle part of the Santa Fe Group, which is the primary water-bearing hydrogeologic unit in the basin and is generally saturated, and (4) the upper part of the Santa Fe Group, which is the most productive water-bearing unit within the Santa Fe Group but is only partially saturated in the north and largely unsaturated in the south and western parts of the Mesilla Basin.The helicopter frequency domain electromagnetic survey results indicated that approximately half of the resistivity values were less than 10 ohm-meters at depths of 50 and 100 feet with a transition where the resistivity values changed from relatively high values (greater than 20 ohm-meters) to relatively low resistivity values (less than 10 ohm-meters) near Vado, New Mexico. Slightly more than 25 percent of the gridded resistivity values from the three-dimensional grid of the combined inverse modeling results of the direct-current resistivity and

Characterization of geochemical constituents and bacterial populations associated with As mobilization in deep and shallow tube wells in Bangladesh.

Science.gov (United States)

Sutton, Nora B; van der Kraan, Geert M; van Loosdrecht, Mark C M; Muyzer, Gerard; Bruining, Johannes; Schotting, Ruud J

2009-04-01

While millions of people drink arsenic-contaminated tube well water across Bangladesh, there is no recent scientific explanation which is able to either comprehensively explain arsenic mobilization or to predict the spatial distribution of affected wells. Rather, mitigation strategies have focused on the sinking of deep tube wells into the currently arsenic-free Pleistocene aquifer. In this study, Bangladesh shallow tube wells identified as contaminated and uncontaminated, as well as deep tube wells, were analyzed for geochemical and in situ microbiological composition. Whereas arsenic was detected in all Holocene aquifer wells, no arsenic was found in wells accessing the Pleistocene aquifer. Bacterial genera, including Comamonadaceae, Acidovorax, Acinetobacter, and Hydrogenophaga, associated with tolerance of high arsenic concentrations, rather than dissimilatory Fe(III) or As(V) reduction, were identified in shallow tube wells, indicating that mobilization may not occur at depth, but is rather due to drawdown of surface contaminated water. Deep tube wells contained microbes indicative of aerobic conditions, including the genera Aquabacterium, Limnobacter, and Roseomonas. It is concluded that through drawdown of arsenic or organic matter, further utilization of the Pleistocene aquifer could result in contamination similar to that observed in the Holocene aquifer.

Mobilization of arsenic and other naturally occurring contaminants in groundwater of the Main Ethiopian Rift aquifers.

Science.gov (United States)

Rango, Tewodros; Vengosh, Avner; Dwyer, Gary; Bianchini, Gianluca

2013-10-01

This study investigates the mechanisms of arsenic (As) and other naturally occurring contaminants (F(-), U, V, B, and Mo) mobilization from Quaternary sedimentary aquifers of the Main Ethiopian Rift (MER) and their enrichment in the local groundwater. The study is based on systematic measurements of major and trace elements as well as stable oxygen and hydrogen isotopes in groundwater, coupled with geochemical and mineralogical analyses of the aquifer rocks. The Rift Valley aquifer is composed of rhyolitic volcanics and Quaternary lacustrine sediments. X-ray fluorescence (XRF) results revealed that MER rhyolites (ash, tuff, pumice and ignimbrite) and sediments contain on average 72 wt. % and 65 wt. % SiO2, respectively. Petrographic studies of the rhyolites indicate predominance of volcanic glass, sanidine, pyroxene, Fe-oxides and plagioclase. The As content in the lacustrine sediments (mean = 6.6 mg/kg) was higher than that of the rhyolites (mean: 2.5 mg/kg). The lacustrine aquifers of the Ziway-Shala basin in the northern part of MER were identified as high As risk zones, where mean As concentration in groundwater was 22.4 ± 33.5 (range of 0.60-190 μg/L) and 54% of samples had As above the WHO drinking water guideline value of 10 μg/L. Field As speciation measurements showed that most of the groundwater samples contain predominantly (~80%) arsenate-As(V) over arsenite-As(III) species. The As speciation together with field data of redox potential (mean Eh = +73 ± 65 mV) and dissolved-O2 (6.6 ± 2.2 mg/L) suggest that the aquifer is predominantly oxidative. Water-rock interactions, including the dissolution of volcanic glass produces groundwater with near-neutral to alkaline pH (range 6.9-8.9), predominance of Na-HCO3 ions, and high concentration of SiO2 (mean: 85.8 ± 11.3 mg/L). The groundwater data show high positive correlation of As with Na, HCO3, U, B, V, and Mo (R(2) > 0.5; p groundwater indicates that Fe-oxides and oxyhydroxides minerals were saturated

Detailed geochemical survey for east-central Minnesota, geology and geochemistry of selected uranium targets

International Nuclear Information System (INIS)

Morey, G.B.; Lively, R.S.

1980-01-01

Results of a detailed geochemical survey of approximately 6820 km 2 in parts of Aitkin, Carlton, Kanabec, and Pine Counties, east-central Minnesota are reported. Geochemical data are presented for 883 groundwater samples and 200 bedrock samples. Although all of the groundwaters in the study area have similar major-element concentrations and therefore presumably a common ancestry, small differences in the minor-element concentrations serve to characterize various aquifers, both in the Quaternary deposits and in the bedrock. All of the aquifers locally yield waters having statistically anomalous concentrations of uranium or radon, but these anomalies are spatially coincident only in a few places and particularly in three geologic environments considered favorable for uranium mineralization. These include the following: (1) Thomson Formation near the unconformably overlying Fond du Lac Formation, (2) Hinckley Sandstone near a major fault system, and (3) Denham Formation near the unconformity with the McGrath Gneiss, particularly where these rocks are faulted and overlain by the Fond du Lac Formation. One additional uranium environment characterized by thin laminae of uraniferous apatite was located in the Thomson Formation during outcrop reconnaissance and sampling. The coincidence of this and other anomalously high uranium values in the bedrock with specific uranium and radon anomalies in the groundwater confirms the usefulness of the hydrogeochemical data to uranium exploration in this glaciated terrane

Long term rise of a free aquifer in Sahel: hydrodynamic and radioisotopic estimations (3H, 14C) of the recharge in SW Niger

International Nuclear Information System (INIS)

Favreau, G.

2001-01-01

This article summarizes an hydrodynamic and geochemical survey carried out in SW Niger in order to estimate the impact of rainfall changes and deforestation on the recharge of the uppermost Cretaceous aquifer. 14 C and 3 H activities of the total dissolved inorganic carbon have been used to quantify the long-term recharge of the aquifer. (J.S.)

Geochemistry of aquifer sediments and arsenic-rich groundwaters from Kandal Province, Cambodia

International Nuclear Information System (INIS)

Rowland, Helen A.L.; Gault, Andrew G.; Lythgoe, Paul; Polya, David A.

2008-01-01

Elevated As is well known to be present in aquifers utilised for drinking water and irrigation in West Bengal and Bangladesh. This problem has also more recently been discovered in other parts of Asia, including Vietnam, Cambodia, Inner Mongolia and the Middle Ganges Plain. Analysis of groundwaters in Kandal Province of Cambodia found waters with comparable geochemistry to the As-rich groundwaters of the West Bengali Delta. Similarities included high but heterogeneous As distributions, predominantly in the form As(III), high Fe, moderate to high HCO 3 - , circumneutral pH, low SO 4 2- and geochemical components indicative of reducing conditions. Good positive correlations between As, Fe, HCO 3 - and NH 4 + , and dissolved organic C is consistent with As release predominantly via microbially mediated reductive dissolution of As bearing Fe(III) oxides. Further evidence for such a process is found from correlations between As, Fe and organic matter from analysis of aquifer sediments, by the presence of goethite in the finer fractions and from the association of As with amorphous, poorly crystalline and well crystallised hydrous Fe oxides. The presence of several high As, but low Fe, wells implies that microbes could have a more direct role in mediating As release via the direct utilisation of Fe(III) or As(V) as electron acceptors. The presence of elevated As in waters with short aquifer residence times (as indicated by their geochemical signature) highlights the possible vulnerability of these aquifers to the influx of surface derived waters, providing an additional source of labile organic C that could exacerbate As release by stimulating microbial activity

Analysis of mineral trapping for CO{sub 2} disposal in deep aquifers

Energy Technology Data Exchange (ETDEWEB)

Xu, Tianfu; Apps, John A.; Pruess, Karsten

2001-07-20

CO{sub 2} disposal into deep aquifers has been suggested as a potential means whereby atmospheric emissions of greenhouse gases may be reduced. However, our knowledge of the geohydrology, geochemistry, geophysics, and geomechanics of CO{sub 2} disposal must be refined if this technology is to be implemented safely, efficiently, and predictably. As a prelude to a fully coupled treatment of physical and chemical effects of CO{sub 2} injection, we have analyzed the impact of CO{sub 2} immobilization through carbonate precipitation. A survey of all major classes of rock-forming minerals, whose alteration would lead to carbonate precipitation, indicated that very few minerals are present in sufficient quantities in aquifer host rocks to permit significant sequestration of CO{sub 2}. We performed batch reaction modeling of the geochemical evolution of three different aquifer mineralogies in the presence of CO{sub 2} at high pressure. Our modeling considered (1) redox processes that could be important in deep subsurface environments, (2) the presence of organic matter, (3) the kinetics of chemical interactions between the host rock minerals and the aqueous phase, and (4) CO{sub 2} solubility dependence on pressure, temperature and salinity of the system. The geochemical evolution under both natural background and CO{sub 2} injection conditions was evaluated. In addition, changes in porosity were monitored during the simulations. Results indicate that CO{sub 2} sequestration by matrix minerals varies considerably with rock type. Under favorable conditions the amount of CO{sub 2} that may be sequestered by precipitation of secondary carbonates is comparable with and can be larger than the effect of CO{sub 2} dissolution in pore waters. The precipitation of ankerite and siderite is sensitive to the rate of reduction of ferric mineral precursors such as glauconite, which in turn is dependent on the reactivity of associated organic material. The accumulation of carbonates in

Cation exchange and CaCO 3 dissolution during artificial recharge of effluent to a calcareous sandstone aquifer

Science.gov (United States)

Goren, Orly; Gavrieli, Ittai; Burg, Avihu; Lazar, Boaz

2011-03-01

SummaryThis research describes a field study and laboratory simulations of the geochemical evolution of groundwater following a recharge of effluent into aquifers. The study was conducted in the soil aquifer treatment (SAT) system of the Shafdan sewage reclamation plant, Israel. The SAT system recharges secondary effluent into the calcareous sandstone sediments of the Israeli Coastal Aquifer as a tertiary treatment. The reclaimed effluent is recovered ca. 500 m off the recharge basin and is used for unlimited irrigation. The laboratory simulations in which effluent was pumped through experimental columns packed with pristine Shafdan sediment showed that the chemical composition of the outflowing water was controlled mainly by cation exchange and CaCO 3 dissolution. Na +, K + and Mg 2+ were adsorbed and Ca 2+ was desorbed during the initial stage of recharge. The equilibrium distribution of the adsorbed cations was: Ca 2+ ˜ 60%, Mg 2+ ˜ 20%, and Na + and K + ˜ 10% each. The Ca 2+ in the Shafdan production wells and in the experimental columns outflow (˜5 meq L -1) was always higher than the Ca 2+ in the recharged effluent (˜3.5 meq L -1), indicating continuous CaCO 3 dissolution. This study demonstrates that besides mixing, a suite of geochemical processes should be considered when assessing groundwater quality following artificial recharge of aquifers.

Multivariate analysis of the heterogeneous geochemical processes controlling arsenic enrichment in a shallow groundwater system.

Science.gov (United States)

Huang, Shuangbing; Liu, Changrong; Wang, Yanxin; Zhan, Hongbin

2014-01-01

The effects of various geochemical processes on arsenic enrichment in a high-arsenic aquifer at Jianghan Plain in Central China were investigated using multivariate models developed from combined adaptive neuro-fuzzy inference system (ANFIS) and multiple linear regression (MLR). The results indicated that the optimum variable group for the AFNIS model consisted of bicarbonate, ammonium, phosphorus, iron, manganese, fluorescence index, pH, and siderite saturation. These data suggest that reductive dissolution of iron/manganese oxides, phosphate-competitive adsorption, pH-dependent desorption, and siderite precipitation could integrally affect arsenic concentration. Analysis of the MLR models indicated that reductive dissolution of iron(III) was primarily responsible for arsenic mobilization in groundwaters with low arsenic concentration. By contrast, for groundwaters with high arsenic concentration (i.e., > 170 μg/L), reductive dissolution of iron oxides approached a dynamic equilibrium. The desorption effects from phosphate-competitive adsorption and the increase in pH exhibited arsenic enrichment superior to that caused by iron(III) reductive dissolution as the groundwater chemistry evolved. The inhibition effect of siderite precipitation on arsenic mobilization was expected to exist in groundwater that was highly saturated with siderite. The results suggest an evolutionary dominance of specific geochemical process over other factors controlling arsenic concentration, which presented a heterogeneous distribution in aquifers. Supplemental materials are available for this article. Go to the publisher's online edition of the Journal of Environmental Science and Health, Part A, to view the supplemental file.

Water-rock interaction and geochemistry of groundwater from the Ain Azel aquifer, Algeria.

Science.gov (United States)

Belkhiri, Lazhar; Mouni, Lotfi; Tiri, Ammar

2012-02-01

Hydrochemical, multivariate statistical, and inverse geochemical modeling techniques were used to investigate the hydrochemical evolution within the Ain Azel aquifer, Algeria. Cluster analysis based on major ion contents defined 3 main chemical water types, reflecting different hydrochemical processes. The first group water, group 1, has low salinity (mean EC = 735 μS/cm). The second group waters are classified as Cl-HCO(3)-alkaline earth type. The third group is made up of water samples, the cation composition of which is dominated by Ca and Mg with anion composition varying from dominantly Cl to dominantly HCO(3) plus SO(4). The varifactors obtained from R-mode FA indicate that the parameters responsible for groundwater quality variations are mainly related to the presence and dissolution of some carbonate, silicate, and evaporite minerals in the aquifer. Inverse geochemical modeling along groundwater flow paths indicates the dominant processes are the consumption of CO(2), the dissolution of dolomite, gypsum, and halite, along with the precipitation of calcite, Ca-montmorillonite, illite, kaolinite, and quartz. © Springer Science+Business Media B.V. 2011

Geochemical and hydrological characterization of shallow aquifer water following a nearby deep CO2 injection in Wellington, Kansas

Science.gov (United States)

Datta, S.; Andree, I.; Johannesson, K. H.; Kempton, P. D.; Barker, R.; Birdie, T. R.; Watney, W. L.

2017-12-01

Salinization or CO2 leakage from local Enhanced Oil Recovery (EOR) projects has become a possible source for contamination and water quality degradation for local irrigation or potable well users in Wellington, Kansas. Shallow domestic and monitoring wells, as well as surface water samples collected from the site, were analyzed for a wide array of geochemical proxies including major and trace ions, rare earth elements (REE), stable isotopes, dissolved organic carbon and dissolved hydrocarbons; these analytes were employed as geotracers to understand the extent of hydrologic continuity throughout the Paleozoic stratigraphic section. Previous research by Barker et al. (2012) laid the foundation through a mineralogical and geochemical investigation of the Arbuckle injection zone and assessment of overlying caprock integrity, which led to the conclusion that the 4,910-5,050' interval will safely sequester CO2 with high confidence of a low leakage potential. EOR operations using CO2 as the injectant into the Mississippian 3,677-3,706' interval was initiated in Jan 2016. Two groundwater sampling events were conducted to investigate any temporal changes in the surface and subsurface waters. Dissolved (Ca+Mg)/Na and Na/Cl mass ratio values of two domestic wells and one monitoring well ranged from 0.67 to 2.01 and 0.19 to 0.39, respectively, whereas a nearby Mississippian oil well had values of 0.20 and 0.62, respectively . δ18O and δ2H ranged from -4.74 to -5.41 ‰VSMOW and -31.4 to -34.3 ‰VSMOW, respectively, among the domestic wells and shallowest monitoring well. Conservative ion relationships in drill-stem-test waters from Arbuckle and Mississippian injection zones displayed significant variability, indicating limited vertical hydrologic communication. Total aquifer connectivity is inconclusive based on the provided data; however, a paleoterrace and incised valley within the study site are thought to be connected through a Mississippian salt plume migration

Isotopic, hydrochemical, and hydrogeological study of deep aquifer of Sfax: First results

International Nuclear Information System (INIS)

Maliki, M. A.; Zouari, K.; Amouri, M.

1996-01-01

The water of the chlorinated sodic with chemical facies deep aquifer of Sfax presents a difference on the level of mineralization between the northern sector with a relatively weak salin charge (average of 3,5 g/l) and the southern sector with an important mineralization (about 10g/l). The mineralization of water in linked to dissolution phenomena. Based on the first isotopic results, it seems that the present refill of the deep aquifer of Sfax is very weak (author)

National Geochemical Survey Locations and Results for Iowa

Data.gov (United States)

Iowa State University GIS Support and Research Facility — The United States Geological Survey (USGS), in collaboration with other state and federal agencies, industry, and academia, is conducting a National Geochemical...

Groundwater quality of the Gulf Coast aquifer system, Houston, Texas, 2010

Science.gov (United States)

Oden, Jeannette H.; Brown, Dexter W.; Oden, Timothy D.

2011-01-01

During March–December 2010, the U.S. Geological Survey, in cooperation with the city of Houston, collected source-water samples from 60 municipal supply wells in the Houston area. These data were collected as part of an ongoing study to determine concentrations, spatial extent, and associated geochemical conditions that might be conducive for mobility and transport of selected naturally occurring contaminants (selected trace elements and radionuclides) in the Gulf Coast aquifer system in the Houston area. In the summers of 2007 and 2008, a reconnaissance-level survey of these constituents in untreated water from 28 municipal supply wells was completed in the Houston area. Included in this report are the complete analytical results for 47 of the 60 samples collected in 2010—those results which were received from the laboratories and reviewed by the authors as of December 31, 2010. All of the wells sampled were screened in the Gulf Coast aquifer system; 22 were screened entirely in the Evangeline aquifer, and the remaining 25 wells contained screened intervals that intersected both Evangeline and Chicot aquifers. The data documented in this report were collected as part of an ongoing study to characterize source-water-quality conditions in untreated groundwater prior to drinking-water treatment. An evaluation of contaminant occurrence in source water provides background information regarding the presence of a contaminant in the environment. Because source-water samples were collected prior to any treatment or blending that potentially could alter contaminant concentrations, the water-quality results documented by this report represent the quality of the source water, not the quality of finished drinking water provided to the public.

Analysis of mineral trapping for CO(sub 2) disposal in deep aquifers; TOPICAL

International Nuclear Information System (INIS)

Xu, Tianfu; Apps, John A.; Pruess, Karsten

2001-01-01

CO(sub 2) disposal into deep aquifers has been suggested as a potential means whereby atmospheric emissions of greenhouse gases may be reduced. However, our knowledge of the geohydrology, geochemistry, geophysics, and geomechanics of CO(sub 2) disposal must be refined if this technology is to be implemented safely, efficiently, and predictably. As a prelude to a fully coupled treatment of physical and chemical effects of CO(sub 2) injection, we have analyzed the impact of CO(sub 2) immobilization through carbonate precipitation. A survey of all major classes of rock-forming minerals, whose alteration would lead to carbonate precipitation, indicated that very few minerals are present in sufficient quantities in aquifer host rocks to permit significant sequestration of CO(sub 2). We performed batch reaction modeling of the geochemical evolution of three different aquifer mineralogies in the presence of CO(sub 2) at high pressure. Our modeling considered (1) redox processes that could be important in deep subsurface environments, (2) the presence of organic matter, (3) the kinetics of chemical interactions between the host rock minerals and the aqueous phase, and (4) CO(sub 2) solubility dependence on pressure, temperature and salinity of the system. The geochemical evolution under both natural background and CO(sub 2) injection conditions was evaluated. In addition, changes in porosity were monitored during the simulations. Results indicate that CO(sub 2) sequestration by matrix minerals varies considerably with rock type. Under favorable conditions the amount of CO(sub 2) that may be sequestered by precipitation of secondary carbonates is comparable with and can be larger than the effect of CO(sub 2) dissolution in pore waters. The precipitation of ankerite and siderite is sensitive to the rate of reduction of ferric mineral precursors such as glauconite, which in turn is dependent on the reactivity of associated organic material. The accumulation of carbonates in

Carbon dioxide (CO2) sequestration in deep saline aquifers and formations: Chapter 3

Science.gov (United States)

Rosenbauer, Robert J.; Thomas, Burt

2010-01-01

Carbon dioxide (CO2) capture and sequestration in geologic media is one among many emerging strategies to reduce atmospheric emissions of anthropogenic CO2. This chapter looks at the potential of deep saline aquifers – based on their capacity and close proximity to large point sources of CO2 – as repositories for the geologic sequestration of CO2. The petrochemical characteristics which impact on the suitability of saline aquifers for CO2 sequestration and the role of coupled geochemical transport models and numerical tools in evaluating site feasibility are also examined. The full-scale commercial CO2 sequestration project at Sleipner is described together with ongoing pilot and demonstration projects.

Solute geochemistry of the Snake River Plain regional aquifer system, Idaho and eastern Oregon

International Nuclear Information System (INIS)

Wood, W.W.; Low, W.H.

1987-01-01

Three geochemical methods were used to determine chemical reactions that control solute concentrations in the Snake River Plain regional aquifer system: (1) calculation of a regional solute balance within the aquifer and of mineralogy in the aquifer framework to identify solute reactions, (2) comparison of thermodynamic mineral saturation indices with plausible solute reactions, and (3) comparison of stable isotope ratios of the groundwater with those in the aquifer framework. The geothermal groundwater system underlying the main aquifer system was examined by calculating thermodynamic mineral saturation indices, stable isotope ratios of geothermal water, geothermometry, and radiocarbon dating. Water budgets, hydrologic arguments, and isotopic analyses for the eastern Snake River Plain aquifer system demonstrate that most, if not all, water is of local meteoric and not juvenile or formation origin. Solute balance, isotopic, mineralogic, and thermodynamic arguments suggest that about 20% of the solutes are derived from reactions with rocks forming the aquifer framework. Reactions controlling solutes in the western Snake river basin are believed to be similar to those in the eastern basin but the regional geothermal system that underlies the Snake river Plain contains total dissolved solids similar to those in the overlying Snake River Plain aquifer system but contains higher concentrations of sodium, bicarbonate, silica, fluoride, sulfate, chloride, arsenic, boron, and lithium, and lower concentrations of calcium, magnesium, and hydrogen. 132 refs., 30 figs., 27 tabs

Dissolved 210Po and 210Pb in Guarani aquifer groundwater, Brazil

International Nuclear Information System (INIS)

Bonotto, D.M.; Caprioglio, L.; Bueno, T.O.; Lazarindo, J.R.

2009-01-01

The huge Guarani aquifer located in the South American continent is a very important resource for the region, and its drinking water quality has been investigated according to international standards, inclusive radiological parameters. This paper describes 210 Po and 210 Pb activity concentration data in groundwater samples collected at the Brazilian portion of Guarani aquifer, that is characterized by a great variability of temperature (18-70 deg. C), pH (4.0-9.9), sodium content (0.3-322 mg/l), bicarbonate content (0.1-318 mg/l), etc. Non-expensive alpha counting following some radiochemical steps for extracting and depositing dissolved 210 Po was used. The results of the measurements for samples collected in duplicate yielded a maximum 210 Po activity concentration of 3.7 mBq/L and a maximum 210 Pb activity concentration of 6.7 mBq/l, that are values greatly lower than the guidance level of 0.1 Bq/l established by the WHO for their presence in drinking water. The high sensitivity of the method allowed its applicability on the identification of complexes geochemical and hydrogeological processes occurring in Guarani aquifer as well on the evaluation of the drinking water quality in terms of dose calculations.

Intrinsic bioremediation of petroleum hydrocarbons in a gas condensate-contaminated aquifer

International Nuclear Information System (INIS)

Gieg, L.M.; McInerney; Tanner, R.S.; Harris, S.H. Jr.; Sublette, K.L.; Suflita, J.M.; Kolhatkar, R.V.

1999-01-01

A study was designed to determine if the intrinsic bioremediation of gas condensate hydrocarbons represented an important fate process in a shallow aquifer underlying a natural gas production site. For over 4 yr, changes in the groundwater, sediment, and vadose zone chemistry in the contaminated portion of the aquifer were interpreted relative to a background zone. Changes included decreased dissolved oxygen and sulfate levels and increased alkalinity, Fe(II), and methane concentrations in the contaminated groundwater, suggesting that aerobic heterotrophic respiration depleted oxygen reserves leaving anaerobic conditions in the hydrocarbon-impacted subsurface. Dissolved hydrogen levels in the contaminated groundwater indicated that sulfate reduction and methanogenesis were predominant biological processes, corroborating the geochemical findings. Furthermore, 10--1000-fold higher numbers of sulfate reducers and methanogens were enumerated in the contaminated sediment relative to background. Putative metabolites were also detected in the contaminated groundwater, including methylbenzylsuccinic acid, a signature intermediate of anaerobic xylene decay. Laboratory incubations showed that benzene, toluene, ethylbenzene, and each of the xylene isomers were biodegraded under sulfate-reducing conditions as was toluene under methanogenic conditions. These results coupled with a decrease in hydrocarbon concentrations in contaminated sediment confirm that intrinsic bioremediation contributes to the attenuation of hydrocarbons in this aquifer

LASTRIG -A Multiple Parametric Method of Assessment of Salinization Vulnerability of a Coastal Aquifer in Pennar Delta, India

Science.gov (United States)

Kesireddy, K.; Mareddy, A.

2007-05-01

Coastal populations are critically dependent upon the coastal aquifers for their freshwater requirements. Excessive withdrawal of groundwater leads to saline incursion and the consequent degradation of quality and quantity of freshwater. The paper describes a multiple parametric method of assessment of vulnerability of the coastal aquifer in Pennar delta, south India, in the context of the hydrogeological, biophysical, geochemical and socioeconomic environments of the delta. Seven parameters, forming the acronym LASTRIG viz. landuse, aquifer type, soil depth, groundwater table, rainfall, soil infiltration and geomorphology are made use in the assessment, and involve the use of remote sensing, GIS and modeling tools. The parameters are weighted, and a suitable ranking system has been designed to quantify the degree of vulnerability of the aquifer for salinization. It has been found that zones with high vulnerability index correlate well with zones of high TDS and chloride contents of groundwater. This observation thus validates the geochemical basis of the proposed LASTRIG system. The new system has been found useful in the management of the groundwater resources of the delta region. It has been made use of identify the aquifer segments which are in danger of being degraded, to enable the decision- makers to design counter measures to avoid further deterioration in water quality. Where the groundwater has already been rendered non-potable because of saline incursion, the LASTRIG index could be made use to identify possible use of that water for drinking by cattle, and for growing of salt-tolerant vegetables (e.g. beetroot and lettuce), and trees (e.g. casuarinas obese, Prosopis juliflora)

Simulation of groundwater flow in the Edwards-Trinity and related aquifers in the Pecos County region, Texas

Science.gov (United States)

Clark, Brian R.; Bumgarner, Johnathan R.; Houston, Natalie A.; Foster, Adam L.

2014-01-01

The Edwards-Trinity aquifer is a vital groundwater resource for agricultural, industrial, and public supply uses in the Pecos County region of western Texas. The U.S. Geological Survey completed a comprehensive, integrated analysis of available hydrogeologic data to develop a numerical groundwater-flow model of the Edwards-Trinity and related aquifers in the study area in parts of Brewster, Jeff Davis, Pecos, and Reeves Counties. The active model area covers about 3,400 square miles of the Pecos County region of Texas west of the Pecos River, and its boundaries were defined to include the saturated areas of the Edwards-Trinity aquifer. The model is a five-layer representation of the Pecos Valley, Edwards-Trinity, Dockum, and Rustler aquifers. The Pecos Valley aquifer is referred to as the alluvial layer, and the Edwards-Trinity aquifer is divided into layers representing the Edwards part of the Edwards-Trinity aquifer and the Trinity part of the Edwards-Trinity aquifer, respectively. The calibration period of the simulation extends from 1940 to 2010. Simulated hydraulic heads generally were in good agreement with observed values; 1,684 out of 2,860 (59 percent) of the simulated values were within 25 feet of the observed value. The average root mean square error value of hydraulic head for the Edwards-Trinity aquifer was 34.2 feet, which was approximately 4 percent of the average total observed change in groundwater-level altitude (groundwater level). Simulated spring flow representing Comanche Springs exhibits a pattern similar to observed spring flow. Independent geochemical modeling corroborates results of simulated groundwater flow that indicates groundwater in the Edwards-Trinity aquifer in the Leon-Belding and Fort Stockton areas is a mixture of recharge from the Barilla and Davis Mountains and groundwater that has upwelled from the Rustler aquifer.

Understanding the fate of sanitation-related nutrients in a shallow sandy aquifer below an urban slum area

Science.gov (United States)

Nyenje, P. M.; Havik, J. C. N.; Foppen, J. W.; Muwanga, A.; Kulabako, R.

2014-08-01

We hypothesized that wastewater leaching from on-site sanitation systems to alluvial aquifers underlying informal settlements (or slums) may end up contributing to high nutrient loads to surface water upon groundwater exfiltration. Hence, we conducted a hydro-geochemical study in a shallow sandy aquifer in Bwaise III parish, an urban slum area in Kampala, Uganda, to assess the geochemical processes controlling the transport and fate of dissolved nutrients (NO3, NH4 and PO4) released from on-site sanitation systems to groundwater. Groundwater was collected from 26 observation wells. The samples were analyzed for major ions (Ca, Mg, Na, Mg, Fe, Mn, Cl and SO4) and nutrients (o-PO4, NO3 and NH4). Data was also collected on soil characteristics, aquifer conductivity and hydraulic heads. Geochemical modeling using PHREEQC was used to determine the level of o-PO4 control by mineral solubility and sorption. Groundwater below the slum area was anoxic and had near neutral pH values, high values of EC (average of 1619 μS/cm) and high concentrations of Cl (3.2 mmol/L), HCO3 (11 mmol/L) and nutrients indicating the influence from wastewater leachates especially from pit latrines. Nutrients were predominantly present as NH4 (1-3 mmol/L; average of 2.23 mmol/L). The concentrations of NO3 and o-PO4 were, however, low: average of 0.2 mmol/L and 6 μmol/L respectively. We observed a contaminant plume along the direction of groundwater flow (NE-SW) characterized by decreasing values of EC and Cl, and distinct redox zones. The redox zones transited from NO3-reducing in upper flow areas to Fe-reducing in the lower flow areas. Consequently, the concentrations of NO3 decreased downgradient of the flow path due to denitrification. Ammonium leached directly into the alluvial aquifer was also partially removed because the measured concentrations were less than the potential input from pit latrines (3.2 mmol/L). We attributed this removal (about 30%) to anaerobic ammonium oxidation

Geochemical and isotopic determination of deep groundwater contributions and salinity to the shallow groundwater and surface water systems, Mesilla Basin, New Mexico, Texas, and Mexico

Science.gov (United States)

Robertson, A.; Carroll, K. C.; Kubicki, C.; Purtshert, R.

2017-12-01

The Mesilla Basin/Conejos-Médanos aquifer system, extending from southern New Mexico to Chihuahua, Mexico, is a priority transboundary aquifer under the 2006 United States­-Mexico Transboundary Aquifer Assessment Act. Declining water levels, deteriorating water quality, and increasing groundwater use by municipal, industrial, and agricultural users on both sides of the international border raise concerns about long-term aquifer sustainability. Relative contributions of present-day and "paleo" recharge to sustainable fresh groundwater yields has not been determined and evidence suggests that a large source of salinity at the distal end of the Mesilla Basin is saline discharge from deep groundwater flow. The magnitude and distribution of those deep saline flow paths are not determined. The contribution of deep groundwater to discharge and salinity in the shallow groundwater and surface water of the Mesilla Basin will be determined by collecting discrete groundwater samples and analyzing for aqueous geochemical and isotopic tracers, as well as the radioisotopes of argon and krypton. Analytes include major ions, trace elements, the stable isotopes of water, strontium and boron isotopes, uranium isotopes, the carbon isotopes of dissolved inorganic carbon, noble gas concentrations and helium isotope ratios. Dissolved gases are extracted and captured from groundwater wells using membrane contactors in a process known as ultra-trace sampling. Gas samples are analyzed for radioisotope ratios of krypton by the ATTA method and argon by low-level counting. Effectiveness of the ultra-trace sampling device and method was evaluated by comparing results of tritium concentrations to the krypton-85 content. Good agreement between the analyses, especially in samples with undetectable tritium, indicates that the ultra-trace procedure is effective and confirms that introduction of atmospheric air has not occurred. The geochemistry data indicate a complex system of geochemical

Hydrogeochemical study of water in some aquifers of the Estado de Mexico

International Nuclear Information System (INIS)

Pena, P.; Lopez, A.; Balcazar, M.; Flores, J.H.; Cardenas, S.; Schubert, M.

2005-01-01

The National Institute of Nuclear Research of Mexico (ININ), has developed a technique that allows to study the association of recharge mechanisms, residence times of the water in the aquifers, as well as the local lithology and the geochemical parameters. The viability of this technique was proven on November 2004 in the aquifers (La Perita, El Tunel y El Pedregal) located in the Asuncion Tepexoyuca, Estado de Mexico. It was observed that so much the aquifer El Tunel like La Perita are used for the human consumption, the aquifer of El Pedregal is used for the fish cultivation. The studies were carried out during March 2003 to November 2004. In the aquifer La Perita the maximum values of the radon concentration (0.76 Bq L -1 ) they were observed in the summertime time (December). In the spring El Tunel the maximum values of the radon concentration (4.08 Bq L -1 ) they were observed in the rainy season (September) this increment can be due to the contributions of the recharge of aquifers that it allows the haulage of the radon of other alternating roads of infiltration of the rain water. Of the physicochemical and radiochemical analyses carried out in the water samples of the studied aquifers, it is deduced that they are waters of good quality since for the human consumption since that they are inside on the maximum permissible limits as for their potability according to national and international standards. Likewise it was observed that the water of the aquifers is a single aquifer, since that its differences they due to the time of permanency of the water inside the aquifer. The classification of the underground water deduced that it is calcic and/or magnesic bi carbonated water belonging to the type of meteoric waters of recent infiltration. (Author)

Uruguay Mining inventory. Florida fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H.; Artignan, D.; Vairon, P.

1982-01-01

This work is about the geochemical prospecting carried out in Florida fotoplano within the framework of Uruguay Mining inventory. In this work were covered 660 km2 obtaining 752 samples for study which were analyzed by Plasma Emission Spectrometry in Orleans BRGM laboratories

GeoChip-based analysis of microbial functional gene diversity in a landfill leachate-contaminated aquifer

Science.gov (United States)

Lu, Zhenmei; He, Zhili; Parisi, Victoria A.; Kang, Sanghoon; Deng, Ye; Van Nostrand, Joy D.; Masoner, Jason R.; Cozzarelli, Isabelle M.; Suflita, Joseph M.; Zhou, Jizhong

2012-01-01

The functional gene diversity and structure of microbial communities in a shallow landfill leachate-contaminated aquifer were assessed using a comprehensive functional gene array (GeoChip 3.0). Water samples were obtained from eight wells at the same aquifer depth immediately below a municipal landfill or along the predominant downgradient groundwater flowpath. Functional gene richness and diversity immediately below the landfill and the closest well were considerably lower than those in downgradient wells. Mantel tests and canonical correspondence analysis (CCA) suggested that various geochemical parameters had a significant impact on the subsurface microbial community structure. That is, leachate from the unlined landfill impacted the diversity, composition, structure, and functional potential of groundwater microbial communities as a function of groundwater pH, and concentrations of sulfate, ammonia, and dissolved organic carbon (DOC). Historical geochemical records indicate that all sampled wells chronically received leachate, and the increase in microbial diversity as a function of distance from the landfill is consistent with mitigation of the impact of leachate on the groundwater system by natural attenuation mechanisms.

Geochemical modeling of reactions and partitioning of trace metals and radionuclides during titration of contaminated acidic sediments.

Science.gov (United States)

Zhang, Fan; Luo, Wensui; Parker, Jack C; Spalding, Brian P; Brooks, Scott C; Watson, David B; Jardine, Philip M; Gu, Baohua

2008-11-01

Many geochemical reactions that control aqueous metal concentrations are directly affected by solution pH. However, changes in solution pH are strongly buffered by various aqueous phase and solid phase precipitation/dissolution and adsorption/desorption reactions. The ability to predict acid-base behavior of the soil-solution system is thus critical to predict metal transport under variable pH conditions. This studywas undertaken to develop a practical generic geochemical modeling approach to predict aqueous and solid phase concentrations of metals and anions during conditions of acid or base additions. The method of Spalding and Spalding was utilized to model soil buffer capacity and pH-dependent cation exchange capacity by treating aquifer solids as a polyprotic acid. To simulate the dynamic and pH-dependent anion exchange capacity, the aquifer solids were simultaneously treated as a polyprotic base controlled by mineral precipitation/ dissolution reactions. An equilibrium reaction model that describes aqueous complexation, precipitation, sorption and soil buffering with pH-dependent ion exchange was developed using HydroGeoChem v5.0 (HGC5). Comparison of model results with experimental titration data of pH, Al, Ca, Mg, Sr, Mn, Ni, Co, and SO4(2-) for contaminated sediments indicated close agreement suggesting that the model could potentially be used to predictthe acid-base behavior of the sediment-solution system under variable pH conditions.

Determining origin of underground water in coal mines by means of natural isotopes and other geochemical parameters

Energy Technology Data Exchange (ETDEWEB)

Dolenec, T; Pezdic, J; Herlec, U; Kuscer, D; Mitrevski, G [Institut Josef Stefan, Ljubljana (Yugoslavia)

1989-07-01

Presents a preliminary report on origin of water in Slovenian brown coal mines. Water, coal and strata samples from the Hrastnik and Ojstro mines were analyzed for changes in chemical composition. Water samples were also analyzed for changes in isotopic composition and inorganic carbon and sulfur contents. Chemical, isotopic and geochemical techniques are described and results are presented with 21 diagrams. An attempt is made to explain the origin and age of water flowing from mine aquifers into mine rooms, and to explain the interdependence of surface and underground water flow. 10 refs.

Uruguay Mining inventory. Minas fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H.; Artignan, D.; Vairon, P.

1982-01-01

This work is about the geochemical prospecting carried out in Minas fotoplano within the framework of Uruguay Mining inventory. In this work were covered 380 km2 obtaining with 433 samples for study which were analized by Plasma Emission Spectrometry in Orleans BRGM laboratories

Geologic, geochemical, microbiologic, and hydrologic characterization at the In Situ Redox Manipulation Test Site

International Nuclear Information System (INIS)

Vermeul, V.R.; Teel, S.S.; Amonette, J.E.

1995-07-01

This report documents results from characterization activities at the In Situ Redox Manipulation (ISRM) Field Test Site which is located within the 100-HR-3 Operable Unit of the US Department of Energy's (DOE's) Hanford Site in Richland, Washington. Information obtained during hydrogeologic characterization of the site included sediment physical properties, geochemical properties, microbiologic population data, and aquifer hydraulic properties. The purpose of obtaining this information was to improve the conceptual understanding of the hydrogeology beneath the ISRM test site and provide detailed, site specific hydrogeologic parameter estimates. The resulting characterization data will be incorporated into a numerical model developed to simulate the physical and chemical processes associated with the field experiment and aid in experiment design and interpretation

GEOCHEMICAL ASSESSMENT OF THE UNCONFINED AQUIFER IN A RECENTLY RECLAIMED WETLAND AREA: A CASE STUDY FROM THE PO RIVER DELTA

Directory of Open Access Journals (Sweden)

Dario Di Giuseppe

2013-09-01

Full Text Available This study focusses on the distribution of main anions and nitrogen species in the unconfined aquifer of a recently reclaimed land. In a 6 ha experimental field, 10 piezometers for water level measurement and groundwater sampling have been installed. After one year of monitoring, results show that the high chloride and ammonium concentrations are due to inherited from the previous brackish conditions and to organic matter mineralization, respectively. Seasonal variations and Cl/Br ratio show that the 1 m deep sub surface drainage system is the main factor conditioning the chemical characteristics and the piezometric depth of the aquifer. 

Water-quality characteristics of quaternary unconsolidated-deposit aquifers and lower tertiary aquifers of the Bighorn Basin, Wyoming and Montana, 1999-2001

Science.gov (United States)

Bartos, Timothy T.; Eddy-Miller, Cheryl A.; Norris, Jody R.; Gamper, Merry E.; Hallberg, Laura L.

2004-01-01

samples with larger concentrations generally were calcium-sodium-sulfate, calcium-sulfate, or sodium-sulfate-type waters. In the lower Tertiary aquifers, samples with fresh waters generally were sodium-bicarbonate or sodium-bicarbonate-sulfate type waters, whereas samples with larger concentrations were sodium-sulfate or calcium-sodium-sulfate types. Concentrations of most trace elements in both types of aquifers generally were small and most were less than applicable USEPA standards. The trace elements that most often did not meet USEPA secondary drinking-water standards were iron and manganese. In fact, the SMCL for manganese was the most frequently exceeded standard; 68 percent of the samples from the Quaternary aquifers and 31 percent of the samples from the lower Tertiary aquifers exceeded the manganese standard. Geochemical conditions may control manganese in both aquifers as concentrations in Quaternary aquifers were negatively correlated with dissolved oxygen concentrations and concentrations in lower Tertiary aquifers decreased with increasing pH. Elevated nitrate concentrations, in addition to detection of pesticides and VOCs in both aquifers, indicated some effects of human activities on ground-water quality. Nitrate concentrations in 36 percent of the wells in Quaternary aquifers and 28 percent of the wells in lower Tertiary aquifers were greater than 1 mg/L, which may indicate ground-water contamination from human sources. The USEPA drinking-water Maximum Contaminant Level (MCL) for nitrate, 10 mg/L, was exceeded in 8 percent of samples collected from Quaternary aquifers and 3 percent from lower Tertiary aquifers. Nitrate concentrations in Quaternary aquifers were positively correlated with the percentage of cropland and other agricultural land (non-cropland), and negatively correlated with rangeland and riparian land. In the lower Tertiary aquifers, nitrate concentrations only were correlated with the percentage of cropland. Concentratio

Potential Risks of Freshwater Aquifer Contamination with Geosequestration

Energy Technology Data Exchange (ETDEWEB)

Jackson, Robert

2013-09-30

Substantial leakage of CO{sub 2} from deep geological strata to shallow potable aquifers is likely to be rare, but chemical detection of potential leakage nonetheless remains an integral component of any safe carbon capture and storage system. CO{sub 2} that infiltrates an unconfined freshwater aquifer will have an immediate impact on water chemistry by lowering pH in most cases and by altering the concentration of total dissolved solids. Chemical signatures in affected waters provide an important opportunity for early detection of leaks. In the presence of CO{sub 2}, trace elements such as Mn, Fe, and Ca can increase by an order of magnitude or more above control concentrations within 100 days. Therefore, these and other elements should be monitored along with pH as geochemical markers of potential CO{sub 2} leaks. Dissolved inorganic carbon and alkalinity can also be rapidly responsive to CO{sub 2} and are stable indicators of a leak. Importantly, such changes may be detectable long before direct changes in CO{sub 2} are observed. The experimental results also suggest that the relative severity of the impact of leaks on overlying drinking-water aquifers should be considered in the selection of CO{sub 2} sequestration sites. One primary selection criteria should be metal and metalloid availability, such as uranium and arsenic abundance, to carefully monitor chemical species that could trigger changes above maximum contaminant levels (MCLs). Overall, the risks of leakage from underground CO{sub 2} storage are real but appear to be manageable if systems are closely monitored.

Solid phases limiting the concentration of dissolved constituents in basalt aquifers of the Columbia Plateau in eastern Washington

International Nuclear Information System (INIS)

Deutsch, W.J.; Jenne, E.A.; Krupka, K.M.

1981-01-01

The purposes of this study were: (1) to provide information on the solid phases which are in apparent equilibrium with ground waters of basalt aquifers, and (2) to further develop the capability of geochemical modeling to support solute transport studies and performance assessments of nuclear waste repositories. The basalt aquifers of the Columbia Plateau in eastern Washington were chosen as the study area because: (1) regional ground-water analyses are readily available, (2) these basalts are a potential medium for a nuclear-waste repository, and (3) mineralogical analyses from local site studies are available

Similar sediment provenance of low and high arsenic aquifers in Bangladesh

Science.gov (United States)

Zheng, Y.; Yang, Q.; Li, S.; Hemming, S. R.; Zhang, Y.; Rasbury, T.; Hemming, G.

2017-12-01

Geogenic arsenic (As) in drinking water, especially in groundwater, is estimated to have affected the health of over 100 million people worldwide, with nearly half of the total at risk population in Bangladesh. Sluggish flow and reducing biogeochemical environment in sedimentary aquifers have been shown as the primary controls for the release of As from sediment to the shallower groundwater in the Holocene aquifer. In contrast, deeper groundwater in the Pleistocene aquifer is depleted in groundwater As and sediment-extractable As. This study assesses the origin of the sediment in two aquifers of Bangladesh that contain distinctly different As levels to ascertain whether the source of the sediment is a factor in this difference through measurements of detrital mica Ar-Ar age, detrital zircon U-Pb age, as well as sediment silicate Sr and Nd isotopes. Whole rock geochemical data were also used to illuminate the extent of chemical weathering. Detrital mica 40Ar/39Ar cooling ages and detrital zircon U-Pb ages show no statistical difference between high-As Holocene sediment and low-As Pleistocene sediment, but suggest an aquifer sediment source of both the Brahmaputra and the Ganges rivers. Silicate 87Sr/86Sr and 143Nd/144Nd further depict a major sediment source from the Brahmaputra river, which is supported by a two end member mixing model using 87Sr/86Sr and Sr concentrations. Pleistocene and Holocene sediments show little difference in weathering of mobile elements including As, while coarser sediments and a longer history of the Pleistocene aquifer suggest that sorting and flushing play more important roles in regulating the contrast of As occurrence between these two aquifers.

Attenuation of landfill leachate by UK Triassic sandstone aquifer materials. 1. Fate of inorganic pollutants in laboratory columns

Science.gov (United States)

Thornton, Steven F.; Tellam, John H.; Lerner, David N.

2000-05-01

The attenuation of inorganic contaminants in acetogenic and methanogenic landfill leachate by calcareous and carbonate-deficient, oxide-rich Triassic sandstone aquifer materials from the English Midlands was examined in laboratory columns. Aqueous equilibrium speciation modelling, simple transport modelling and chemical mass balance approaches are used to evaluate the key processes and aquifer geochemical properties controlling contaminant fate. The results indicate that leachate-rock interactions are dominated by ion-exchange processes, acid-base and redox reactions and sorption/precipitation of metal species. Leachate NH 4 is attenuated by cation exchange with the aquifer sediments; however, NH 4 migration could be described with a simple model using retardation factors. Organic acids in the acetogenic leachate buffered the system pH at low levels during flushing of the calcareous aquifer material. In contrast, equilibrium with Al oxyhydroxide phases initially buffered pH (˜4.5) during flushing of the carbonate-deficient sandstone with methanogenic leachate. This led to the mobilisation of sorbed and oxide-bound heavy metals from the aquifer sediment which migrated as a concentrated pulse at the leachate front. Abiotic reductive dissolution of Mn oxyhydroxides on each aquifer material by leachate Fe 2+ maintains high concentrations of dissolved Mn and buffers the leachate inorganic redox system. This feature is analogous to the Mn-reducing zones found in leachate plumes and in the experiments provides a sink for the leachate Fe load and other heavy metals. The availability of reactive solid phase Mn oxyhydroxides limits the duration of redox buffering and Fe attenuation by these aquifer sediments. Aquifer pH and redox buffering capacity exert a fundamental influence on leachate inorganic contaminant fate in these systems. The implications for the assessment of aquifer vulnerability at landfills are discussed and simple measurements of aquifer properties which

Process-based reactive transport model to quantify arsenic mobility during aquifer storage and recovery of potable water.

Science.gov (United States)

Wallis, Ilka; Prommer, Henning; Pichler, Thomas; Post, Vincent; Norton, Stuart B; Annable, Michael D; Simmons, Craig T

2011-08-15

Aquifer storage and recovery (ASR) is an aquifer recharge technique in which water is injected in an aquifer during periods of surplus and withdrawn from the same well during periods of deficit. It is a critical component of the long-term water supply plan in various regions, including Florida, USA. Here, the viability of ASR as a safe and cost-effective water resource is currently being tested at a number of sites due to elevated arsenic concentrations detected during groundwater recovery. In this study, we developed a process-based reactive transport model of the coupled physical and geochemical mechanisms controlling the fate of arsenic during ASR. We analyzed multicycle hydrochemical data from a well-documented affected southwest Floridan site and evaluated a conceptual/numerical model in which (i) arsenic is initially released during pyrite oxidation triggered by the injection of oxygenated water (ii) then largely complexes to neo-formed hydrous ferric oxides before (iii) being remobilized during recovery as a result of both dissolution of hydrous ferric oxides and displacement from sorption sites by competing anions.

Distribution of sulphur isotopes of sulphates in groundwaters from the principal artesian aquifer of Florida and the Edwards aquifer of Texas, United States of America

International Nuclear Information System (INIS)

Rightmire, C.T.; Pearson, F.J. Jr.; Back, W.; Rye, R.O.; Hanshaw, B.B.

1974-01-01

New information on the sources of sulphate dissolved in groundwater is obtainable from the measurement of the sulphur isotope composition of sulphates. Field studies in the Floridan aquifer, Florida, and the Edwards aquifer, Texas, show that the use of sulphur isotope data in conjunction with hydrologic and geochemical techniques permits refinements of interpretation. In the Floridan the interpretation of the chemical data, particularly the SO 4 2- concentration and the SO 4 2- /Cl - ratio, leads to the conclusion that recharging maritime rainfall, solution of intraformational gypsum, and mixing with ocean-like saline waters are the sources of sulphate in the groundwater. Sulphur isotope data substantiate this interpretation. The Edwards in the area studied can be separated into two hydrologie units on the basis of water chemistry and aquifer characteristics. The sulphide-free waters in the part of the aquifer upgradient from a distinct sulphide boundary are low in sulphate (less than 100 mg/1) and contain no sulphide. The waters downgradient from that boundary contain greater than 150 mg/1 sulphate and all contain measurable quantities of sulphide. Interpretation of the SO 4 2- concentration and SO 4 2- /Cl ratio on the basis of the Florida study leads to the erroneous conclusion that the solution of intraformational gypsum is again a major source of sulphate in the sulphide-free part of the aquifer. Isotope analyses, however, show that the gypsum is likely to be Permian in age and introduced into the aquifer by the recharge water. The absence of evidence for enrichment in 34 S in the sulphate in the sulphide-bearing portion of the aquifer leads to the possibility of H 2 S migration upgradient from downdip oil fields. (author)

Uruguay mining Inventory: Geochemical prospecting results of Valentines mapping

International Nuclear Information System (INIS)

Spangenberg, J.; Filippini, J.

1985-01-01

This work is about geochemical prospecting carried out into the Uruguay mining inventory framework. In this case the survey was in Valentines mapping. Florida, Durazno and Treinta y Tres provinces of Uruguay .

Investigating geochemical aspects of managed aquifer recharge by column experiments with alternating desalinated water and groundwater.

Science.gov (United States)

Ronen-Eliraz, Gefen; Russak, Amos; Nitzan, Ido; Guttman, Joseph; Kurtzman, Daniel

2017-01-01

Managed aquifer recharge (MAR) events are occasionally carried out with surplus desalinated seawater that has been post-treated with CaCO 3 in infiltration ponds overlying the northern part of the Israeli Coastal Aquifer. This water's chemical characteristics differ from those of any other water recharged to the aquifer and of the natural groundwater. As the MAR events are short (hours to weeks), the sediment under the infiltration ponds will intermittently host desalinated and natural groundwater. As part of comprehensive research on the influence of those events, column experiments were designed to simulate the alternation of the two water types: post-treated desalinated seawater (PTDES) and natural groundwater (GW). Each experiment included three stages: (i) saturation with GW; (ii) inflow of PTDES; (iii) inflow of GW. Three runs were conducted, each with different sediments extracted from the field and representing a different layer below the infiltration pond: (i) sand (<1% CaCO 3 ), (ii) sand containing 7% CaCO 3 , and (iii) crushed calcareous sandstone (35% CaCO 3 ). The results from all columns showed enrichment of K + and Mg 2+ (up to 0.4meq/L for 20 pore volumes) when PTDES replaced GW, whereas an opposite trend of Ca 2+ depletion (up to 0.5meq/L) was observed only in the columns that contained a high percentage of CaCO 3 . When GW replaced PTDES, depletion of Mg 2+ and K + was noted. The results indicated that adsorption/desorption of cations are the main processes causing the observed enrichment/depletion. It was concluded that the high concentration of Ca 2+ (relative to the total concentration of cations) and the low concentration of Mg 2+ in the PTDES relative to natural GW are the factors controlling the main sediment-water interaction. The enrichment of PTDES with Mg 2+ may be viewed as an additional post-treatment. Copyright © 2016 Elsevier B.V. All rights reserved.

Geophysical and Hydrogeological Evaluation of Pliocene Aquifer in East Esna, Egypt

Science.gov (United States)

Basheer, Alhussein Adham; Mosaad, Sayed

2018-01-01

The current study of East Esna area was selected due to its prosperous conditions. In this area, the reclamation of agricultural land is increasing and the population is growing, which necessitate an equivalent development of groundwater. The main aim of the study was to estimate geometrical and qualitative characteristics of the study aquifer. This will help to have a systematic view of the hydrogeological setting in the area of investigation, categorize and evaluate the influential factors of existence, quality, and protection of the groundwater. The geometrical characteristics of the local aquifer were revealed by using 45 VES and TEM soundings. The study area has two main aquifers. Both hosted in sandstone of Issawia formation. The brackish groundwater lies above the fresh groundwater, which is shielded by Esna shale at the bottom. The source of feeding to these aquifers is direct leakage of runoff and rain on the east side with sporadic leaks from the waters of the River Nile on the west side. The analyzed groundwater samples are geochemically homogenous, indicating that their genesis is rain water. They also belong to Na-Ca-SO4-Cl type. The groundwater in the study area is assessed for drinking, household, livestock, and agricultural purposes. The current study recommends some advises for groundwater development in the study area.

Reaction of subsurface coastal aquifers to climate and land use changes in Greece: modelling of groundwater refreshening patterns under natural recharge conditions

Science.gov (United States)

Lambrakis, N.; Kallergis, G.

2001-05-01

This paper studies the multicomponent ion exchange process and freshening time under natural recharge conditions for three coastal aquifers in Greece. Due to over-pumping and the dry years of 1980-1990 decline in groundwater quality has been observed in most of the Greek coastal aquifers. This decline is caused by a lack of reliable water resource management, water abstraction from great depths, and seawater intrusion resulting in a rise of the fresh/salt water interface (salinisation process) due to a negative water balance. The reverse phenomenon, which should lead to groundwater freshening, is a long process. The freshening process shows chromatographic patterns that are due to chemical reactions such as calcite dissolution and cation exchange, and simultaneously occurring transport and dispersion processes. Using the geochemical simulation codes PHREEQE and PHREEQM (Parkhurst et al., US Geol. Surv. Water Resour. Invest., 80-96 (1980) 210; Appelo and Postma, Geochemistry, Groundwater and Pollution (1994)), these patterns were analysed and the above-mentioned processes were simulated for carefully selected aquifers in Peloponnesus and Crete (Greece). Aquifers of the Quaternary basin of Glafkos in Peloponnesus, the Neogene formations in Gouves, Crete, and the carbonate aquifer of Malia, Crete, were examined as representative examples of Greek coastal aquifer salinisation. The results show that when pumping was discontinued, the time required for freshening under natural conditions of the former two aquifers is long and varies between 8000 and 10,000 years. The Malia aquifer on the other hand, has a freshening time of 15 years. Freshening time was shown to depend mainly on cation exchange capacities and the recharge rate of the aquifers.

Mercury mobilization and speciation linked to bacterial iron oxide and sulfate reduction: A column study to mimic reactive transfer in an anoxic aquifer.

Science.gov (United States)

Hellal, Jennifer; Guédron, Stéphane; Huguet, Lucie; Schäfer, Jörg; Laperche, Valérie; Joulian, Catherine; Lanceleur, Laurent; Burnol, André; Ghestem, Jean-Philippe; Garrido, Francis; Battaglia-Brunet, Fabienne

2015-09-01

Mercury (Hg) mobility and speciation in subsurface aquifers is directly linked to its surrounding geochemical and microbial environment. The role of bacteria on Hg speciation (i.e., methylation, demethylation and reduction) is well documented, however little data is available on their impact on Hg mobility. The aim of this study was to test if (i) Hg mobility is due to either direct iron oxide reduction by iron reducing bacteria (IRB) or indirect iron reduction by sulfide produced by sulfate reducing bacteria (SRB), and (ii) to investigate its subsequent fate and speciation. Experiments were carried out in an original column setup combining geochemical and microbiological approaches that mimic an aquifer including an interface of iron-rich and iron depleted zones. Two identical glass columns containing iron oxides spiked with Hg(II) were submitted to (i) direct iron reduction by IRB and (ii) to indirect iron reduction by sulfides produced by SRB. Results show that in both columns Hg was leached and methylated during the height of bacterial activity. In the column where IRB are dominant, Hg methylation and leaching from the column was directly correlated to bacterial iron reduction (i.e., Fe(II) release). In opposition, when SRB are dominant, produced sulfide induced indirect iron oxide reduction and rapid adsorption of leached Hg (or produced methylmercury) on neoformed iron sulfides (e.g., Mackinawite) or its precipitation as HgS. At the end of the SRB column experiment, when iron-oxide reduction was complete, filtered Hg and Fe concentrations increased at the outlet suggesting a leaching of Hg bound to FeS colloids that may be a dominant mechanism of Hg transport in aquifer environments. These experimental results highlight different biogeochemical mechanisms that can occur in stratified sub-surface aquifers where bacterial activities play a major role on Hg mobility and changes in speciation. Copyright © 2015 Elsevier B.V. All rights reserved.

Dissolved {sup 210}Po and {sup 210}Pb in Guarani aquifer groundwater, Brazil

Energy Technology Data Exchange (ETDEWEB)

Bonotto, D.M. [Departamento de Petrologia e Metalogenia, Universidade Estadual Paulista (UNESP), Av. 24-A No. 1515, C.P. 178, CEP 13506-900 Rio Claro, Sao Paulo (Brazil)], E-mail: danielbonotto@yahoo.com.br; Caprioglio, L.; Bueno, T.O.; Lazarindo, J.R. [Departamento de Petrologia e Metalogenia, Universidade Estadual Paulista (UNESP), Av. 24-A No. 1515, C.P. 178, CEP 13506-900 Rio Claro, Sao Paulo (Brazil)

2009-03-15

The huge Guarani aquifer located in the South American continent is a very important resource for the region, and its drinking water quality has been investigated according to international standards, inclusive radiological parameters. This paper describes {sup 210}Po and {sup 210}Pb activity concentration data in groundwater samples collected at the Brazilian portion of Guarani aquifer, that is characterized by a great variability of temperature (18-70 deg. C), pH (4.0-9.9), sodium content (0.3-322 mg/l), bicarbonate content (0.1-318 mg/l), etc. Non-expensive alpha counting following some radiochemical steps for extracting and depositing dissolved {sup 210}Po was used. The results of the measurements for samples collected in duplicate yielded a maximum {sup 210}Po activity concentration of 3.7 mBq/L and a maximum {sup 210}Pb activity concentration of 6.7 mBq/l, that are values greatly lower than the guidance level of 0.1 Bq/l established by the WHO for their presence in drinking water. The high sensitivity of the method allowed its applicability on the identification of complexes geochemical and hydrogeological processes occurring in Guarani aquifer as well on the evaluation of the drinking water quality in terms of dose calculations.

Multielement geochemical reconnaissance for uranium in the Palmyrides region of central Syria

International Nuclear Information System (INIS)

Jubeli, Y.M.; Hale, M.

1988-01-01

Multielement reconnaissance geochemistry coupled with ground scintillation gamma ray measurements has been used to investigate the dispersion patterns of uranium and other major and trace elements in the arid Palmyrides region of central Syria. Over 500 geochemical samples of outcropping rock, wadi and playa sediments, overburden and groundwaters were taken over an area of approximately 9000 sq km. Most samples were analyzed for 25 major and trace elements by nebulization ICPAES; for As, Sb, Bi and Se by hydride generation and ICPAES; and for U, Th and La and other REE by neutron activation analysis. The resulting data were interpreted with the aid of univariate and multivariate statistical methods. The areal distributions of U, its associated elements, multivariate geochemical functions and factor scores were mapped using computer graphics. Results of the factor analysis indicate that the primary lithogeochemical dispersion patterns of uranium and associated elements are controlled by a combination of structural, lithological and environmental factors. Uranium and associated elements have subsequently been leached out of the phosphorite and other U enriched clayey limestones and carbonate rocks into the hydro- geologic regime. Redistribution of these elements is taking place along fracture zones and major faults. A degree of urnaium accumulation in a Neogene aquifer of the Ad-Daww basin is evident

Groundwater residence time and movement in the Maltese islands - A geochemical approach

Energy Technology Data Exchange (ETDEWEB)

Stuart, M.E., E-mail: mest@bgs.ac.uk [British Geological Survey, Wallingford, Oxfordshire OX10 8BB (United Kingdom); Maurice, L. [British Geological Survey, Wallingford, Oxfordshire OX10 8BB (United Kingdom); Heaton, T.H.E. [British Geological Survey, NERC Isotope Geoscience Laboratory, Keyworth, Nottinghamshire NG12 5GG (United Kingdom); Sapiano, M.; Micallef Sultana, M. [Malta Resources Authority, Marsa MRS 9065 (Malta); Gooddy, D.C.; Chilton, P.J. [British Geological Survey, Wallingford, Oxfordshire OX10 8BB (United Kingdom)

2010-05-15

The Maltese islands are composed of two limestone aquifers, the Upper and Lower Coralline Limestone separated by an aquitard, the 'Blue Clay'. The Lower Coralline Limestone is overlain in part by the poorly permeable Globigerina Limestone. The upper perched aquifers are discontinuous and have very limited saturated thickness and a short water level response time to rainfall. Frequent detections of coliforms suggest a rapid route to groundwater. However, the unsaturated zone has a considerable thickness in places and the primary porosity of the Upper Coralline Limestone is high, so there is likely to be older recharge by slow matrix flow as well as rapid recharge from fractures. Measurement of SF{sub 6} from a pumping station in a deep part of one of the perched aquifers indicated a mean saturated zone age of about 15 a. The Main Sea Level aquifers (MSL) on both Malta and Gozo have a large unsaturated thickness as water levels are close to sea level. On Malta, parts of the aquifer are capped by the perched aquifers and more extensively by the Globigerina Limestone. The limited detection of coliform bacteria suggests only some rapid recharge from the surface via fractures or karst features. Transmissivity is low and {sup 3}H and CFC/SF{sub 6} data indicate that saturated zone travel times are in the range 15-40 a. On Gozo the aquifer is similar but is more-extensively capped by impermeable Blue Clay. CFC data show the saturated zone travel time is from 25 a to possibly more than 60 a. Groundwater age is clearly related to the extent of low-permeability cover. The {delta}{sup 13}C signature of groundwater is related to the geochemical processes which occur along the flowpath and is consistent with residence time ages in the sequence; perched aquifers < Malta MSL < Gozo MSL. The {sup 18}O and {sup 2}H enriched isotopic signature of post 1983 desalinated water can be seen in more-modern groundwater, particularly the urbanized areas of the perched and Malta MSL

Managed aquifer recharge in weathered crystalline basement aquifers in India: Monitoring of the effect of tank infiltration on water quality over several monsoon events

Science.gov (United States)

Alazard, Marina; Boisson, Alexandre; Maréchal, Jean-Christophe; Dewandel, Benoît; Perrin, Jérôme; Pettenati, Marie; Picot-Colbeaux, Géraldine; Ahmed, Shakeel; Thiéry, Dominique; Kloppmann, Wolfram

2015-04-01

Managed aquifer recharge (MAR) structures like percolation tanks are considered by the Indian national and regional governments as major option for tackling declining groundwater levels due to overexploitation for irrigation purposes (Boisson et al., 2014). Their main purpose is to restore groundwater availability under strong climatic and anthropogenic pressure. Furthermore, MAR-induced dilution with fresh surface water is generally expected to improve groundwater quality with respect to both anthropogenic and geogenic contaminants (total mineralisation, nitrates, chlorides, sulphates and fluoride contents). The impact of a percolation tank on groundwater quality was investigated in a context that is typical for hydro-climatic and geological settings in southern and eastern India: fractured crystalline basement aquifers overlain by a weathering zone under semi-arid climate. Water level data and geochemical indicators (stable isotopes and major ions) were monitored for both groundwater and surface water, over several successive monsoon events. In case of high to very high water levels, the groundwater quality is globally improved. However, in a few cases, the quality of the groundwater can be negatively impacted due to leaching of salts under the tank, particularly during the first rain events of the monsoon. Geogenic fluoride contents in groundwater, induced by water-rock interaction and enhanced by recycling of agricultural return flow under paddy fields, is found to be relatively stable over the year. This finding points out that the underlying processes, mainly dissolution of F-bearing phases like fluorapatites combined with Ca/Na cation exchange and calcite precipitation, both limiting the possibility of F-removal via fluorite precipitation (Pettenati et al., 2013, 2014), are not impacted by the hydrological conditions. This work highlights the complexity of the recharge processes in crystalline aquifers, enhanced by the variability of hydrological conditions

Determination of 222Rn and its physico-chemical and biological characteristics in aquifers of Toluca valley

International Nuclear Information System (INIS)

Hernandez, A.; Aranda, P.; Ceballos, S.; Cruz, D.; Jauregui, B.; Lopez, R.; Pena, P.; Salazar, S.; Segovia, N.; Tamez, E.

1997-01-01

In this work it is realized a geochemical study which includes the evaluation of 222 Rn concentration in drinking water wells at Toluca city and a spring water of Almoloya de Juarez municipality at State of mexico. the same is studied about evolution of 222 Rn concentration in water of the hydrating which supply it to those wells. the geochemical evaluation also covers the determination of major and minor elements or trace and the biological analysis of water. The study includes two seasonal cycles, the low water mark one and other the rainy for being able to evaluate the aquifers reloading effects in the water composition. (Author)

Arsenic enrichment and mobilization in the Holocene alluvial aquifers of the Chapai-Nawabganj district, Bangladesh: A geochemical and statistical study

International Nuclear Information System (INIS)

Reza, A.H.M. Selim; Jean, Jiin-Shuh; Lee, Ming-Kuo; Yang, Huai-Jen; Liu, Chia-Chuan

2010-01-01

Research highlights: → Four factors (i.e., salinity factor, As-enrichment factor, reduction factor, and hardness factor) control groundwater geochemistry. → Hydrochemical facies analysis showed that most of the water samples are dominated by Ca and HCO 3 ions. → Cluster 1 water types are highly enriched in As; an alternative water source is thus needed for domestic water supply. Possible solutions are to install tube wells in the deeper Pleistocene aquifers or use clean surface water sources such as reservoirs or rain water. → Cluster 4 water types contain low concentration As, below the Bangladesh standard ( 4 , total dissolved solids (TDS), and electrical conductivity (EC) are grouped under the first factor representing the salinity sources of waters. The second factor, represented by As and Mn, is related to As mobilization processes. The third factor of Fe and alkalinity is strongly influenced by bacterial Fe(III) reduction which would raise both Fe and HCO 3 - concentrations in water. The fourth factor of Ca and Mg reflects the hardness of the Ca-HCO 3 type of groundwater, which is confirmed by the hydrochemical facies analysis. Cluster analysis leads to the formulation of four water types including highly, moderately, and slightly As-enriched groundwater as well as groundwater with elevated SO 4 2- , from anthropogenic sources. Multivariate analyses of the geochemical parameters suggest that Fe- and Mn-oxyhydroxides and mineral phases of phyllosilicates (e.g., biotite) are the main hosts of As in the sediments. Statistical analysis also shows that As is closely associated with Fe and Mn in sediments while As is positively correlated with Mn in groundwater. These correlations along with results of sequential leaching experiments suggest that reductive dissolution of MnOOH and FeOOH mediated by anaerobic bacteria represents an important mechanism for releasing As into the groundwater.

Relationship between pyrite Stability and arsenic mobility during aquifer storage and recovery in southwest central Florida.

Science.gov (United States)

Jones, Gregg W; Pichler, Thomas

2007-02-01

Elevated arsenic concentrations are common in water recovered from aquifer storage and recovery (ASR) systems in west-central Florida that store surface water. Investigations of the Suwannee Limestone of the Upper Floridan aquifer, the storage zone for ASR systems, have shown that arsenic is highest in pyrite in zones of high moldic porosity. Geochemical modeling was employed to examine pyrite stability in limestone during simulated injections of surface water into wells open only to the Suwannee Limestone with known mineralogy and water chemistry. The goal was to determine if aquifer redox conditions could be altered to the degree of pyrite instability. Increasing amounts of injection water were added to native storage-zone water, and resulting reaction paths were plotted on pyrite stability diagrams. Native storage-zone water plotted within the pyrite stability field, indicating that conditions were sufficiently reducing to allow for pyrite stability. Thus, arsenic is immobilized in pyrite, and its groundwater concentration should be low. This was corroborated by analysis of water samples, none of which had arsenic concentrations above 0.036 microg/L. During simulation, however, as injection/native storage-zone water ratios increased, conditions became less reducing and pyrite became unstable. The result would be release of arsenic from limestone into storage-zone water.

Arsenic Contamination in Groundwater of Bangladesh: Perspectives on Geochemical, Microbial and Anthropogenic Issues

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Shafi M. Tareq

2011-11-01

Full Text Available A groundwater, sediment and soil chemistry and mineralogical study has been performed to investigate the sources and mobilization process of Arsenic (As in shallow aquifers of Bangladesh. The groundwater from the shallow aquifers is characterized by high concentrations of Arsenic (47.5–216.8 µg/L, iron (0.85–5.83 mg/L, and phosphate, along with high electrical conductivity (EC. The groundwater has both very low oxidation-reduction potential (Eh and dissolved oxygen (DO values indicating reducing conditions. By contrast, the deep aquifers and surface waters (pond, canal have very low concentrations of Arsenic ( < 6 µg/L, iron (0.12–0.39 mg/L, and phosphate along with a relatively low EC. Furthermore, the values of Eh and DO are high, indicating oxic to suboxic conditions. Arsenic is inversely correlated with Eh values in the upper aquifer, whereas no relationship in the deeper aquifer is observed. These results suggest that As mobilization is clearly linked to the development of reducing conditions. The clayey silt, enriched in Fe, Mn, Al oxides and organic matter, and deposited in the middle unit of shallow aquifers, contains moderately high concentrations of As, whereas the sediments of deep aquifers and silty mud surface soils from paddy fields and ponds contain a low content of As (Daudkandi area. Arsenic is strongly correlated with the concentrations of Fe, Mn and Al oxides in the core samples from the Daudkandi and Marua areas. Arsenic is present in the oxide phase of Fe and Mn, phyllosilicate minerals and in organic matter in sediments. This study suggests that adsorption or precipitation of As-rich Fe oxyhydroxide on the surface or inner sites of biotite might be responsible for As concentrations found in altered biotite minerals by Seddique et al. Microbially or geochemically mediated reductive dissolution of Fe oxyhydroxides is the main mechanism for As release. The reducing conditions are caused by respiratory decomposition of

Pathogen Decay during Managed Aquifer Recharge at Four Sites with Different Geochemical Characteristics and Recharge Water Sources.

Science.gov (United States)

Sidhu, J P S; Toze, S; Hodgers, L; Barry, K; Page, D; Li, Y; Dillon, P

2015-09-01

Recycling of stormwater water and treated effluent via managed aquifer recharge (MAR) has often been hampered because of perceptions of low microbiological quality of recovered water and associated health risks. The goal of this study was to assess the removal of selected pathogens in four large-scale MAR schemes and to determine the influence of aquifer characteristics, geochemistry, and type of recharge water on the pathogen survival times. Bacterial pathogens tested in this study had the shortest one log removal time (, 200 d). Human adenovirus and rotavirus were relatively persistent under anaerobic conditions (, >200 d). Human adenovirus survived longer than all the other enteric virus tested in the study and hence could be used as a conservative indicator for virus removal in groundwater during MAR. The results suggest that site-specific subsurface conditions such as groundwater chemistry can have considerable influence on the decay rates of enteric pathogens and that viruses are likely to be the critical pathogens from a public health perspective. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Hydrology and geochemistry of a slag-affected aquifer and chemical characteristics of slag-affected ground water, northwestern Indiana and northeastern Illinois

Science.gov (United States)

Bayless, E. Randall; Greeman, T.K.; Harvey, C.C.

1998-01-01

Slag is a by-product of steel manufacturing and a ubiquitous fill material in northwestern Indiana. Ground water associated with slag deposits generally is characterized by high pH and elevated concentrations of many inorganic water-quality constituents. The U.S. Geological Survey, in cooperation with the Indiana Department of Environmental Management, conducted a study in northwestern Indiana from June 1995 to September 1996 to improve understanding of the effects of slag deposits on the water quality of a glacial-outwash aquifer. The Bairstow Landfill, a slag-fill deposit overlying the Calumet aquifer near Hammond, Indiana, was studied to represent conditions in slag-deposit settings that are common in northwestern Indiana. Ground water from 10 observation wells, located in four nests at the site, and surface water from the adjacent Lake George were analyzed for values of field-measured parameters and concentrations of major ions, nutrients, trace elements, and bulk properties. Solid-phase samples of slag and aquifer sediment collected during drilling were examined with X-ray diffraction and geochemical digestion and analysis. Concentrations of calcium, potassium, sodium, and sulfate were highest in wells screened partly or fully in slag. Potassium concentrations in ground water ranged from 2.9 to 120 milligrams per liter (mg/L), were highest in water from slag deposits, and decreased with depth. The highest concentrations for aluminum, barium, molybdenum, nickel, and selenium were in water from the slag. Silica concentrations were highest in wells screened directly beneath the slag?aquifer interface, and magnesium concentrations were highest in intermediate and deep aquifer wells. Silica concentrations in shallow and intermediate aquifer wells ranged from 27 to 41 mg/L and were about 10 times greater than those in water from slag deposits. The highest concentrations for chromium, lead, and zinc were in ground water from immediately below the slag?aquifer

Hydrogeochemical characteristics of groundwater in the coal-bearing aquifer of the Wugou coal mine, northern Anhui Province, China

Science.gov (United States)

Chen, Song; Gui, Herong

2017-07-01

Major ions, trace elements, and isotope concentrations were measured in 11 representative groundwater samples that were collected from a series of aquifers in the Wugou coal mine, Anhui Province. The geochemical characteristics of the groundwater samples were examined using conventional graphical and multivariate statistical approaches, and the results showed that almost all of the groundwater samples collected from the coal-bearing aquifer were the Na-SO4 type, whereas the samples from the Quaternary and the limestone aquifer were the Ca-SO4 and Na-Cl types, respectively. The groundwater in the study area is not suitable for drinking without treatment because of the higher values of total dissolved solids and other parameters, whereas the lower value of the sodium adsorption ratio indicates that it can be used for irrigation. The total rare earth element concentrations ranged from 0.0398 to 0.1874 mg/L, and had an average of 0.075 mg/L. There were negative cerium and positive europium anomalies in the groundwater. The δD and δ 18O values in groundwater ranged from -9.01 to -8.81 ‰, and from -74.7 to -71.4 ‰, respectively. Meteoric water with variable degrees of evaporation is the main source of the groundwater in the coal-bearing aquifer.

Geochemical Constraints for Mercury's PCA-Derived Geochemical Terranes

Science.gov (United States)

Stockstill-Cahill, K. R.; Peplowski, P. N.

2018-05-01

PCA-derived geochemical terranes provide a robust, analytical means of defining these terranes using strictly geochemical inputs. Using the end members derived in this way, we are able to assess the geochemical implications for Mercury.

Processes of water rock interaction in the Turonian aquifer of Oum Er-Rabia Basin, Morocco

Science.gov (United States)

Ettazarini, Said

2005-12-01

Possible water rock interaction processes, in the Moroccan basin of Oum Er-Rabia, were discussed by a geochemical study of groundwater from the Turonian limestone aquifer, the most important water resource in the region. Different types of water according to the classification of Piper were defined. Waters have shown an evolution from dominant CHO3 Ca Mg type through mixed to SO4 Cl Ca Mg type. The use of geochemical diagrams and chemical speciation modeling method has shown that water rock interaction is mainly controlled by carbonate and anhydrite dissolution, ion exchange and reverse ion exchange processes. Water rock equilibrium conditions are favorable for the precipitation of calcite, dolomite, kaolinite and magnesian smectite.

Changing the scale of hydrogeophysical aquifer heterogeneity characterization

Science.gov (United States)

Paradis, Daniel; Tremblay, Laurie; Ruggeri, Paolo; Brunet, Patrick; Fabien-Ouellet, Gabriel; Gloaguen, Erwan; Holliger, Klaus; Irving, James; Molson, John; Lefebvre, Rene

2015-04-01

Contaminant remediation and management require the quantitative predictive capabilities of groundwater flow and mass transport numerical models. Such models have to encompass source zones and receptors, and thus typically cover several square kilometers. To predict the path and fate of contaminant plumes, these models have to represent the heterogeneous distribution of hydraulic conductivity (K). However, hydrogeophysics has generally been used to image relatively restricted areas of the subsurface (small fractions of km2), so there is a need for approaches defining heterogeneity at larger scales and providing data to constrain conceptual and numerical models of aquifer systems. This communication describes a workflow defining aquifer heterogeneity that was applied over a 12 km2 sub-watershed surrounding a decommissioned landfill emitting landfill leachate. The aquifer is a shallow, 10 to 20 m thick, highly heterogeneous and anisotropic assemblage of littoral sand and silt. Field work involved the acquisition of a broad range of data: geological, hydraulic, geophysical, and geochemical. The emphasis was put on high resolution and continuous hydrogeophysical data, the use of direct-push fully-screened wells and the acquisition of targeted high-resolution hydraulic data covering the range of observed aquifer materials. The main methods were: 1) surface geophysics (ground-penetrating radar and electrical resistivity); 2) direct-push operations with a geotechnical drilling rig (cone penetration tests with soil moisture resistivity CPT/SMR; full-screen well installation); and 3) borehole operations, including high-resolution hydraulic tests and geochemical sampling. New methods were developed to acquire high vertical resolution hydraulic data in direct-push wells, including both vertical and horizontal K (Kv and Kh). Various data integration approaches were used to represent aquifer properties in 1D, 2D and 3D. Using relevant vector machines (RVM), the mechanical and

Mining inventory of Uruguay. Polanco fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H; Artignan, D; Vairon, P

1982-01-01

This work is about the geochemical prospecting carried out in Polanco fotoplano within the framework of Uruguay Mining inventory . In this work were covered 660 km2 obtaining 685 samples for study which were analyzed by Plasma Emission Spectrometry in Orleans BRGM laboratories

Water-Rock Interactions in the Peridotite Aquifer of the Oman-UAE Ophiolite: Strontium Isotopic Ratio and Geochemical Evolution of Groundwater

Science.gov (United States)

Bompard, Nicolas; Matter, Juerg; Teagle, Damon

2016-04-01

The peridotite aquifer in Wadi Tayin, Sultanate of Oman, is a perfect example of natural carbonation of ultramafic rocks. In situ mineral carbonation is considered the most safest and permanent option of CO2 Capture and Sequestration (CCS). However, the process itself is yet to be characterised and a better understanding of the mechanisms involved in natural mineral carbonation is needed before geo-engineering it. We used the 87Sr/86Sr system to follow the water-rock interactions along the groundwater flowpath in the peridotite aquifer and to determine the sources of divalent cations (Mg2+, Ca2+) required for mineral carbonation. The Sr-isotope data of groundwater show that the aquifer rocks are the main source for divalent cations (Mg2+, Ca2+ and Sr2+) and secondary carbonates are their main sink. The groundwater 87Sr/86Sr ratio evolves with its pH: from 87Sr/86Sr = 0.7087 (n=3) to 0.7082 (n=8) between pH 7 and 8, and from 0.7086 (n=6) at pH 9 to 0.07075 (n=9) at pH 11. This evolution seems to support a two-step model for the water-rock interactions in the peridotite aquifer. From pH 7 to 8, secondary Ca-carbonate precipitation buffers the pH rise resulting from peridotite serpentinisation. From pH 9 to 11, peridotite serpentinisation drives the pH to alkaline condition. The change from a Mg-rich to a Ca-rich groundwater at pH 9 seems to confirm the two-step model.

Hydrogeological study of the aquifer system of the northern Sahara in the Algero-Tunisian border: A case study of Oued Souf region

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Halassa, Younes; Zeddouri, Aziez; Mouhamadou, Ould Babasy; Kechiched, Rabah; Benhamida, Abdeldjebbar Slimane

2018-05-01

The aquifer system in The Algero-Tunisian border and Chotts region is mainly composed of two aquifers: The first is the Complex Terminal (CT) and the second is the Intercalary aquifer (CI). This study aims the identification and spatial evolution of factors that controlling the water quality in the Complex Terminal aquifer (CT) in the Chotts region (Oued Souf region - Southeastern of Algeria). The concentration of major elements, temperature, pH and salinity were monitored during 2015 in 34 wells from the CT aquifer. The geological, geophysical, hydrogeological and hydrochemical methods were applied in order to carried out a model for the investigated aquifer system and to characterize the hydrogeological and the geochemical behavior, as well as the geometrical and the lithological configuration. Multivariate statistical analyses such as Principal Component Analysis (PCA) were also used for the treatment of several data. Results show that the salinity follows the same regional distribution of Chloride, Sodium, Magnesium, Sulfate and Calcium. Note that the salinity shows low contents in the upstream part of investigated region suggesting restricted dissolution of salts. Hydro-chemical study and saturation indexes highlight the dominance of the dissolution and the precipitation of calcite, dolomite, anhydrite, gypsum and halite. The PCA analysis indicates that Na+, Cl-, Ca2+, Mg2+, SO42- and K+ variables that influence the water mineralization.

New isotopic evidence for the origin of groundwater from the Nubian Sandstone Aquifer in the Negev, Israel

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Vengosh, A.; Hening, S.; Ganor, J.; Mayer, B.; Weyhenmeyer, C.E.; Bullen, T.D.; Paytan, A.

2007-01-01

The geochemistry and isotopic composition (H, O, S, Osulfate, C, Sr) of groundwater from the Nubian Sandstone (Kurnub Group) aquifer in the Negev, Israel, were investigated in an attempt to reconstruct the origin of the water and solutes, evaluate modes of water-rock interactions, and determine mean residence times of the water. The results indicate multiple recharge events into the Nubian sandstone aquifer characterized by distinctive isotope signatures and deuterium excess values. In the northeastern Negev, groundwater was identified with deuterium excess values of ???16???, which suggests local recharge via unconfined areas of the aquifer in the Negev anticline systems. The ??18OH2O and ??2H values (-6.5??? and -35.4???) of this groundwater are higher than those of groundwater in the Sinai Peninsula and southern Arava valley (-7.5??? and -48.3???) that likewise have lower deuterium excess values of ???10???. Based on the geochemical differences between groundwater in the unconfined and confined zones of the aquifer, a conceptual geochemical model for the evolution of the groundwater in the Nubian sandstone aquifer has been reconstructed. The isotopic composition of shallow groundwater from the unconfined zone indicates that during recharge oxidation of pyrite to SO4 (??34SSO4 ???-13???; ??18OSO4 ???+7.7???) and dissolution of CaCO3 (87Sr/86Sr ???0.70787; ??13CDIC = -3.7???) occur. In the confined zone of the aquifer, bacterial SO4 reduction removes a significant part of dissolved SO42 -, thereby modifying its isotopic composition (??34SSO4 ???-2???; ??18OSO4 ???+8.5???) and liberating dissolved inorganic C that contains little or no radiocarbon (14C-free) with low ??13CDIC values (contribution of external groundwater sources to the Nubian Sandstone aquifer, resulting in further modifications of the groundwater chemical and isotopic signatures. In the northeastern Negev, it is shown that SO4-rich groundwater from the underlying Jurassic aquifer contributes

Comparison of aquifer characteristics derived from local and regional aquifer tests.

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Randolph, R.B.; Krause, R.E.; Maslia, M.L.

1985-01-01

A comparison of the aquifer parameter values obtained through the analysis of a local and a regional aquifer test involving the same area in southeast Georgia is made in order to evaluate the validity of extrapolating local aquifer-test results for use in large-scale flow simulations. Time-drawdown and time-recovery data were analyzed by using both graphical and least-squares fitting of the data to the Theis curve. Additionally, directional transmissivity, transmissivity tensor, and angle of anisotropy were computed for both tests. -from Authors Georgia drawdown transmissivity regional aquifer tests

Heat storage in the Hettangian aquifer in Berlin - results from a column experiment

Science.gov (United States)

Milkus, Chri(Sch)augott

2015-04-01

Aquifer Thermal Energy Storage (ATES) is a sustainable alternative for storage and seasonal availability of thermal energy. However, its impact on the subsurface flow regime is not well known. In Berlin (Germany), the Jurassic (Hettangian) sandstone aquifer with highly mineralized groundwater (TDS 27 g/L) is currently used for heat storage. The aim of this study was to examine the hydrogeochemical changes that are caused by the induced temperature shift and its effects on the hydraulic permeability of the aquifer. Column experiments were conducted, in which stainless steel columns were filled with sediment from the aquifer and flushed with native groundwater for several weeks. The initial temperature of the experiment was 20°C, comparable to the in-situ conditions within the aquifer. After reaching equilibrium between sediment and water, the temperature was increased to simulate heating of the aquifer. During the experiment, physical and chemical parameters (pH, ORP, dissolved oxygen and dissolved carbon dioxide) were measured at the outflow of the column and the effluent water was sampled. Using a Scanning Electron Microscope, the deposition of precipitated minerals and biofilm on sediment grains was analyzed. Changes in hydraulic properties of the sediment were studied by the use of tracer tests with Uranin.

Uruguay Mining inventory. Las Animas fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H.; Spangenberg, J.

1981-01-01

This work is about the geochemical prospecting carried out in Las Animas fotoplano within the framework of Uruguay Mining inventory. In this work were covered 660 km2 obtaining 738 samples for study which were analyzed by Plasma Emission Spectrometry in Orleans BRGM laboratories.

Hydrochemical evaluation and identification of geochemical processes in the shallow and deep wells in the Ramganga Sub-Basin, India.

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Rajmohan, Natarajan; Patel, Neelam; Singh, Gaurav; Amarasinghe, Upali A

2017-09-01

Groundwater samples were collected from 44 wells in the Ramganga Sub-Basin (RSB), India, and analysed for major ions, nutrients and trace metals. The primary goal of this study is to evaluate the hydrochemistry and to identify the geochemical processes that govern the water chemistry in the shallow and deep tube wells in the study area using geochemical methods. The knowledge of changes in hydrochemistry of the aquifers is important for both groundwater recharge and use in the region. This study found that there are substantial differences of water chemistry between shallow and deep wells. In the shallow wells, the average concentrations of total dissolved solid (TDS), Na, K, Ca, Mg, HCO 3 , Cl, SO 4 , NO 3 , PO 4 , F, Cu, Mn, Fe and Cr are twofold higher than the deep wells. The concentrations of dissolved silica in the groundwater do not vary with the depth, which implies that the variation in the water chemistry is not due to mineral dissolution alone. Major ion ratios and saturation indices suggest that the water chemistry is predominantly controlled by dissolution of carbonate minerals, silicate weathering and ion exchange reactions. Thermodynamic evaluation (ion activity ratios and stability filed diagrams) indicates that the kaolinite and gibbsite controlled the water chemistry in the both shallow and deep wells. In addition, the groundwater chemistry in the shallow wells is affected by the vertical infiltration of contaminated water from surface contamination sources and nitrification process. In the deep wells, absence of NO 3 and low concentrations of Cl, SO 4 , PO 4 and F imply the role of regional flow and denitrification in the groundwater. Results concluded that proper management plan is necessary to protect the shallow aquifer in the RSB since shallow aquifer pumping is less expensive than the deeper one.

Characterising aquifer treatment for pathogens in managed aquifer recharge.

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Page, D; Dillon, P; Toze, S; Sidhu, J P S

2010-01-01

In this study the value of subsurface treatment of urban stormwater during Aquifer Storage Transfer Recovery (ASTR) is characterised using quantitative microbial risk assessment (QMRA) methodology. The ASTR project utilizes a multi-barrier treatment train to treat urban stormwater but to date the role of the aquifer has not been quantified. In this study it was estimated that the aquifer barrier provided 1.4, 2.6, >6.0 log(10) removals for rotavirus, Cryptosporidium and Campylobacter respectively based on pathogen diffusion chamber results. The aquifer treatment barrier was found to vary in importance vis-à-vis the pre-treatment via a constructed wetland and potential post-treatment options of UV-disinfection and chlorination for the reference pathogens. The risk assessment demonstrated that the human health risk associated with potable reuse of stormwater can be mitigated (disability adjusted life years, DALYs aquifer is integrated with suitable post treatment options into a treatment train to attenuate pathogens and protect human health.

Effects of Sea Level Rise on Groundwater Flow Paths in a Coastal Aquifer System

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Morrissey, S. K.; Clark, J. F.; Bennett, M. W.; Richardson, E.; Stute, M.

2008-05-01

Changes in groundwater flow in the Floridan aquifer system, South Florida, from the rise in sea level at the end of the last glacial period may be indicative of changes coastal aquifers will experience with continued sea level rise. As sea level rises, the hydraulic head near the coast increases. Coastal aquifers can therefore experience decreased groundwater gradients (increased residence times) and seawater intrusion. Stable isotopes of water, dissolved noble gas temperatures, radiocarbon and He concentrations were analyzed in water collected from 68 wells in the Floridan aquifer system throughout South Florida. Near the recharge area, geochemical data along groundwater flow paths in the Upper Floridan aquifer show a transition from recently recharged groundwater to glacial-aged water. Down gradient from this transition, little variation is apparent in the stable isotopes and noble gas recharge temperatures, indicating that most of the Upper Floridan aquifer contains groundwater recharged during the last glacial period. The rapid 120-meter rise in sea level marking the end of the last glacial period increased the hydraulic head in the Floridan aquifer system near the coast, slowing the flow of groundwater from the recharge area to the ocean and trapping glacial-aged groundwater. The raised sea level also flooded half of the Florida platform and caused seawater to intrude into the Lower Floridan. This circulation of seawater in the Lower Floridan continues today as our data indicate that the groundwater is similar to modern seawater with a freshwater component entering vertically from the recharge area to the Upper Floridan.

Processes Governing Alkaline Groundwater Chemistry within a Fractured Rock (Ophiolitic Mélange Aquifer Underlying a Seasonally Inhabited Headwater Area in the Aladağlar Range (Adana, Turkey

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Cüneyt Güler

2017-01-01

Full Text Available The aim of this study was to investigate natural and anthropogenic processes governing the chemical composition of alkaline groundwater within a fractured rock (ophiolitic mélange aquifer underlying a seasonally inhabited headwater area in the Aladağlar Range (Adana, Turkey. In this aquifer, spatiotemporal patterns of groundwater flow and chemistry were investigated during dry (October 2011 and wet (May 2012 seasons utilizing 25 shallow hand-dug wells. In addition, representative samples of snow, rock, and soil were collected and analyzed to constrain the PHREEQC inverse geochemical models used for simulating water-rock interaction (WRI processes. Hydrochemistry of the aquifer shows a strong interseasonal variability where Mg–HCO3 and Mg–Ca–HCO3 water types are prevalent, reflecting the influence of ophiolitic and carbonate rocks on local groundwater chemistry. R-mode factor analysis of hydrochemical data hints at geochemical processes taking place in the groundwater system, that is, WRI involving Ca- and Si-bearing phases; WRI involving amorphous oxyhydroxides and clay minerals; WRI involving Mg-bearing phases; and atmospheric/anthropogenic inputs. Results from the PHREEQC modeling suggested that hydrogeochemical evolution is governed by weathering of primary minerals (calcite, chrysotile, forsterite, and chromite, precipitation of secondary minerals (dolomite, quartz, clinochlore, and Fe/Cr oxides, atmospheric/anthropogenic inputs (halite, and seasonal dilution from recharge.

Development Report on the Idaho National Laboratory Sitewide Three-Dimensional Aquifer Model

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Thomas R. Wood; Catherine M. Helm-Clark; Hai Huang; Swen Magnuson; Travis McLing; Brennon Orr; Michael J. Rohe; Mitchell A. Plummer; Robert Podgorney; Erik Whitmore; Michael S. Roddy

2007-09-01

A sub-regional scale, three-dimensional flow model of the Snake River Plain Aquifer was developed to support remediation decisions for Waste Area Group 10, Operable Unit 10 08 at the Idaho National Laboratory (INL) Site. This model has been calibrated primarily to water levels and secondarily to groundwater velocities interpreted from stable isotope disequilibrium studies and the movement of anthropogenic contaminants in the aquifer from facilities at the INL. The three-dimensional flow model described in this report is one step in the process of constructing a fully three-dimensional groundwater flow and contaminant transport model as prescribed in the Idaho National Engineering and Environmental Laboratory Operable Unit 10-08 Sitewide Groundwater Model Work Plan. An updated three-dimensional hydrogeologic conceptual model is presented along with the geologic basis for the conceptual model. Sediment-dominated three-dimensional volumes were used to represent the geology and constrain groundwater flow as part of the conceptual model. Hydrological, geochemical, and geological data were summarized and evaluated to infer aquifer behavior. A primary observation from development and evaluation of the conceptual model was that relative to flow on a regional scale, the aquifer can be treated with steady-state conditions. Boundary conditions developed for the three-dimensional flow model are presented along with inverse simulations that estimate parameterization of hydraulic conductivity. Inverse simulations were performed using the pilot-point method to estimate permeability distributions. Thermal modeling at the regional aquifer scale and at the sub-regional scale using the inverted permeabilities is presented to corroborate the results of the flow model. The results from the flow model show good agreement with simulated and observed water levels almost always within 1 meter. Simulated velocities show generally good agreement with some discrepancies in an interpreted low

A geochemical and geophysical reappraisal to the significance of the recent unrest at Campi Flegrei caldera (Southern Italy)

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Moretti, Roberto; De Natale, Giuseppe; Troise, Claudia

2017-04-01

Volcanic unrest at calderas involve complex interaction between magma, hydrothermal fluids and crustal stress and strain. Campi Flegrei caldera (CFc), located in the Naples (Italy) area and characterised by the highest volcanic risk on Earth for the extreme urbanisation, undergoes unrest phenomena involving several meters of uplift and intense shallow micro-seismicity since several decades. Despite unrest episodes display in the last decade only moderate ground deformation and seismicity, current interpretations of geochemical data point to a highly pressurized hydrothermal system. We show that at CFc, the usual assumption of vapour-liquid coexistence in the fumarole plumes leads to largely overestimated hydrothermal pressures and, accordingly, interpretations of elevated unrest. By relaxing unconstrained geochemical assumptions, we infer an alternative model yielding better agreement between geophysical and geochemical observations. The model reconciles discrepancies between what observed 1) for two decades since the 1982-84 large unrest, when shallow magma was supplying heat and fluids to the hydrothermal system, and 2) in the last decade. Compared to the 1980's unrest, the post-2005 phenomena are characterized by much lower aquifers overpressure and magmatic involvement, as indicated by geophysical data and despite large changes in geochemical indicators. Our interpretation points out a model in which shallow sills, intruded during 1969-1984, have completely cooled, so that fumarole emissions are affected now by deeper, CO2-richer, magmatic gases producing a relatively modest heating and overpressure of the hydrothermal system. Our results do have important implications on the short-term eruption hazard assessment and on the best strategies for monitoring and interpreting geochemical data.

The relationship of the Yucca Mountain repository block to the regional ground-water system: A geochemical model

International Nuclear Information System (INIS)

Matuska, N.A.; Hess, J.W.

1989-08-01

Yucca Mountain, in southern Nevada, is being studied by the Department of Energy and the State of Nevada as the site of a high-level nuclear waste repository. Geochemical and isotopic modeling were used in this study to define the relationship of the volcanic tuff aquifers and aquitards to the underlying regional carbonate ground-water system. The chemical evolution of a ground water as it passes through a hypothetical tuffaceous aquifer was developed using computer models PHREEQE, WATEQDR and BALANCE. The tuffaceous system was divided into five parts, with specific mineralogies, reaction steps and temperatures. The initial solution was an analysis of a soil water from Rainier Mesa. The ending solution in each part became the initial solution in the next part. Minerals consisted of zeolites, smectites, authigenic feldspars and quartz polymorphs from described diagentic mineral zones. Reaction steps were ion exchange with zeolites. The solution from the final zone, Part V, was chosen as most representative, in terms of pH, element molalities and mineral solubilities, of tuffaceous water. This hypothetical volcanic water from Part V was mixed with water from the regional carbonate aquifer, and the results compared to analyses of Yucca Mountain wells. Mixing and modeling attempts were conducted on wells in which studies indicated upward flow

Application of cluster analysis to geochemical compositional data for identifying ore-related geochemical anomalies

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Zhou, Shuguang; Zhou, Kefa; Wang, Jinlin; Yang, Genfang; Wang, Shanshan

2017-12-01

Cluster analysis is a well-known technique that is used to analyze various types of data. In this study, cluster analysis is applied to geochemical data that describe 1444 stream sediment samples collected in northwestern Xinjiang with a sample spacing of approximately 2 km. Three algorithms (the hierarchical, k-means, and fuzzy c-means algorithms) and six data transformation methods (the z-score standardization, ZST; the logarithmic transformation, LT; the additive log-ratio transformation, ALT; the centered log-ratio transformation, CLT; the isometric log-ratio transformation, ILT; and no transformation, NT) are compared in terms of their effects on the cluster analysis of the geochemical compositional data. The study shows that, on the one hand, the ZST does not affect the results of column- or variable-based (R-type) cluster analysis, whereas the other methods, including the LT, the ALT, and the CLT, have substantial effects on the results. On the other hand, the results of the row- or observation-based (Q-type) cluster analysis obtained from the geochemical data after applying NT and the ZST are relatively poor. However, we derive some improved results from the geochemical data after applying the CLT, the ILT, the LT, and the ALT. Moreover, the k-means and fuzzy c-means clustering algorithms are more reliable than the hierarchical algorithm when they are used to cluster the geochemical data. We apply cluster analysis to the geochemical data to explore for Au deposits within the study area, and we obtain a good correlation between the results retrieved by combining the CLT or the ILT with the k-means or fuzzy c-means algorithms and the potential zones of Au mineralization. Therefore, we suggest that the combination of the CLT or the ILT with the k-means or fuzzy c-means algorithms is an effective tool to identify potential zones of mineralization from geochemical data.

Recharge sources and geochemical evolution of groundwater in the Quaternary aquifer at Atfih area, the northeastern Nile Valley, Egypt

Science.gov (United States)

El-Sayed, Salah Abdelwahab; Morsy, Samah M.; Zakaria, Khalid M.

2018-06-01

This study addresses the topic of recharge sources and evolution of groundwater in the Atfih area situated in the northeastern part of the Nile Valley, Egypt. Inventory of water wells and collection of groundwater and surface water samples have been achieved. Water samples are analyzed for major ions according to the American Society for Testing and Materials and for the environmental isotopes analysis (oxygen-18 and deuterium) by using a Triple Liquid Isotopic Water Analyzer (Los Gatos). The groundwater is available from the Quaternary aquifer formed mainly of graded sand and gravel interbedded with clay lenses. The hydrogeologic, hydrogeochemical and isotopic investigations indicate the hydrodynamic nature of the aquifer, where different flow paths, recharge sources and evolution mechanisms are distinguished. The directions of groundwater flow are from E, W and S directions suggesting the contribution from Nile River, the Eocene aquifer and the Nile basin, respectively. The groundwater altitudes range from 13 m (MSL) to 44 m (MSL). The hydraulic gradient varies between 0.025 and 0.0015. The groundwater is alkaline (pH > 7) and has salinity ranging from fresh to brackish water (TDS between 528 mg/l and 6070 mg/l). The observed wide range in the ionic composition and water types reflects the effect of different environmental and geological conditions through which the water has flowed. The isotopic compositions of groundwater samples vary between -14.13‰ and +23.56 for δD and between - 2.91‰ and +3.10 for δ18O. The isotopic data indicates that the Quaternary aquifer receive recharge from different sources including the Recent Nile water, surplus irrigation water, old Nile water before the construction of Aswan High Dam, surface runoff of local rains and Eocene aquifer. Evaporation, water rock interaction and mixing between different types of waters are the main processes in the groundwater evolution. Major suggestions are presented to develop the aquifer

Insight into Groundwater Flow within a Crystalline Aquifer. Case Study of the Ursuya Mount, Northern Basque Country (France)

International Nuclear Information System (INIS)

Jaunat, J.; Huneau, F.; Dupuy, A.; Franceschi, M.; Coustumer, P. Le; Celle-Jeanton, H.

2011-01-01

The Ursuya Mount is one of the main water supplies of the Northern Basque Country. A study is being conducted since 2009 on this aquifer in order to improve the knowledge on its potential and its hydrodynamics properties. Two hydrological cycles are required to get the necessary data to meet the following objectives: clarifying the aquifer potential of the site both quantitatively and qualitatively; determining the geographic and seasonal variations; understanding the origin and the flow pattern of the groundwater; evaluating the groundwater residence times and the areas of preferential recharge. Here, we present only some geochemical and isotopic data. Thus, structural or hydrodynamic approaches will not be discussed.

PHAST Version 2-A Program for Simulating Groundwater Flow, Solute Transport, and Multicomponent Geochemical Reactions

Science.gov (United States)

Parkhurst, David L.; Kipp, Kenneth L.; Charlton, Scott R.

2010-01-01

The computer program PHAST (PHREEQC And HST3D) simulates multicomponent, reactive solute transport in three-dimensional saturated groundwater flow systems. PHAST is a versatile groundwater flow and solute-transport simulator with capabilities to model a wide range of equilibrium and kinetic geochemical reactions. The flow and transport calculations are based on a modified version of HST3D that is restricted to constant fluid density and constant temperature. The geochemical reactions are simulated with the geochemical model PHREEQC, which is embedded in PHAST. Major enhancements in PHAST Version 2 allow spatial data to be defined in a combination of map and grid coordinate systems, independent of a specific model grid (without node-by-node input). At run time, aquifer properties are interpolated from the spatial data to the model grid; regridding requires only redefinition of the grid without modification of the spatial data. PHAST is applicable to the study of natural and contaminated groundwater systems at a variety of scales ranging from laboratory experiments to local and regional field scales. PHAST can be used in studies of migration of nutrients, inorganic and organic contaminants, and radionuclides; in projects such as aquifer storage and recovery or engineered remediation; and in investigations of the natural rock/water interactions in aquifers. PHAST is not appropriate for unsaturated-zone flow, multiphase flow, or density-dependent flow. A variety of boundary conditions are available in PHAST to simulate flow and transport, including specified-head, flux (specified-flux), and leaky (head-dependent) conditions, as well as the special cases of rivers, drains, and wells. Chemical reactions in PHAST include (1) homogeneous equilibria using an ion-association or Pitzer specific interaction thermodynamic model; (2) heterogeneous equilibria between the aqueous solution and minerals, ion exchange sites, surface complexation sites, solid solutions, and gases; and

Spatial Distribution of Field Physico-Chemical Parameters in the Vulcano Island (Italy Coastal Aquifer: Volcanological and Hydrogeological Implications

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Paolo Madonia

2015-06-01

Full Text Available Vulcano, the southernmost of the Aeolian island arc (Italy, is characterized by a shallow coastal aquifer resulting from the mixing of seawater, meteoric recharge and volcanogenic fluids. The aquifer has been intensively studied during the last decades, but a comprehensive hydrogeological model has never been developed due to the lack of direct information about the litho-stratigraphic columns of the wells and the depth of water bearing levels. We present and discuss here the time and spatial analysis of water table elevation, temperature and electric conductivity data, acquired during the last 20 years in 33 wells located at Vulcano Island, with the aim of developing a groundwater circulation scheme able to fit the field observations. We retrieved a circulation scheme characterized by an intricate geometry of flow paths driven by horizontal and vertical permeability variations, accounting for the strong variability of geochemical data evidenced in this area by the related scientific literature. Extending these results to a general context, particular care must be taken in approaching the study of aquifers in volcanic islands, because a strong, small spatial scale variability of the hydrogeochemical parameters is expected, and a reliable knowledge of the local conditions is required for developing successful groundwater circulation schemes.

Seasonal Influences on Ground-Surface Water Interactions in an Arsenic-Affected Aquifer in Cambodia

Science.gov (United States)

Richards, L. A.; Magnone, D.; Van Dongen, B.; Bryant, C.; Boyce, A.; Ballentine, C. J.; Polya, D. A.

2015-12-01

Millions of people in South and Southeast Asia consume drinking water daily which contains dangerous levels of arsenic exceeding health-based recommendations [1]. A key control on arsenic mobilization in aquifers in these areas has been controversially identified as the interaction of 'labile' organic matter contained in surface waters with groundwaters and sediments at depth [2-4], which may trigger the release of arsenic from the solid- to aqueous-phase via reductive dissolution of iron-(hyr)oxide minerals [5]. In a field site in Kandal Province, Cambodia, which is an arsenic-affected area typical to others in the region, there are strong seasonal patterns in groundwater flow direction, which are closely related to monsoonal rains [6] and may contribute to arsenic release in this aquifer. The aim of this study is to explore the implications of the high susceptibility of this aquifer system to seasonal changes on potential ground-surface water interactions. The main objectives are to (i) identify key zones where there are likely ground-surface water interactions, (ii) assess the seasonal impact of such interactions and (iii) quantify the influence of interactions using geochemical parameters (such as As, Fe, NO3, NH4, 14C, 3T/3He, δ18O, δ2H). Identifying the zones, magnitude and seasonal influence of ground-surface water interactions elucidates new information regarding potential locations/pathways of arsenic mobilization and/or transport in affected aquifers and may be important for water management strategies in affected areas. This research is supported by NERC (NE/J023833/1) to DP, BvD and CJB and a NERC PhD studentship (NE/L501591/1) to DM. References: [1] World Health Organization, 2008. [2] Charlet & Polya (2006), Elements, 2, 91-96. [3] Harvey et al. (2002), Science, 298, 1602-1606. [4] Lawson et al. (2013), Env. Sci. Technol. 47, 7085 - 7094. [5] Islam et al. (2004), Nature, 430, 68-71. [6] Benner et al. (2008) Appl. Geochem. 23(11), 3072 - 3087.

Geochemistry of shallow ground water in coastal plain environments in the southeastern United States: implications for aquifer susceptibility

International Nuclear Information System (INIS)

Tesoriero, Anthony J.; Spruill, Timothy B.; Eimers, Jo L.

2004-01-01

Ground-water chemistry data from coastal plain environments have been examined to determine the geochemical conditions and processes that occur in these areas and assess their implications for aquifer susceptibility. Two distinct geochemical environments were studied to represent a range of conditions: an inner coastal plain setting having more well-drained soils and lower organic carbon (C) content and an outer coastal plain environment that has more poorly drained soils and high organic C content. Higher concentrations of most major ions and dissolved inorganic and organic C in the outer coastal plain setting indicate a greater degree of mineral dissolution and organic matter oxidation. Accordingly, outer coastal plain waters are more reducing than inner coastal plain waters. Low dissolved oxygen (O 2 ) and nitrate (NO 3 - ) concentrations and high iron (Fe) concentrations indicate that ferric iron (Fe (III)) is an important electron acceptor in this setting, while dissolved O 2 is the most common terminal electron acceptor in the inner coastal plain setting. The presence of a wide range of redox conditions in the shallow aquifer system examined here underscores the importance of providing a detailed geochemical characterization of ground water when assessing the intrinsic susceptibility of coastal plain settings. The greater prevalence of aerobic conditions in the inner coastal plain setting makes this region more susceptible to contamination by constituents that are more stable under these conditions and is consistent with the significantly (p 3 - found in this setting. Herbicides and their transformation products were frequently detected (36% of wells sampled), however concentrations were typically low (<0.1 μg/L). Shallow water table depths often found in coastal plain settings may result in an increased risk of the detection of pesticides (e.g., alachlor) that degrade rapidly in the unsaturated zone

The University of Minnesota aquifer thermal energy storage (ATES) field test facility -- system description, aquifer characterization, and results of short-term test cycles

Energy Technology Data Exchange (ETDEWEB)

Walton, M.; Hoyer, M.C.; Eisenreich, S.J.; Holm, N.L.; Holm, T.R.; Kanivetsky, R.; Jirsa, M.A.; Lee, H.C.; Lauer, J.L.; Miller, R.T.; Norton, J.L.; Runke, H. (Minnesota Geological Survey, St. Paul, MN (United States))

1991-06-01

Phase 1 of the Aquifer Thermal Energy Storage (ATES) Project at the University of Minnesota was to test the feasibility, and model, the ATES concept at temperatures above 100{degrees}C using a confined aquifer for the storage and recovery of hot water. Phase 1 included design, construction, and operation of a 5-MW thermal input/output field test facility (FTF) for four short-term ATES cycles (8 days each of heat injection, storage, and heat recover). Phase 1 was conducted from May 1980 to December 1983. This report describes the FTF, the Franconia-Ironton-Galesville (FIG) aquifer used for the test, and the four short-term ATES cycles. Heat recovery; operational experience; and thermal, chemical, hydrologic, and geologic effects are all included. The FTF consists of monitoring wells and the source and storage well doublet completed in the FIG aquifer with heat exchangers and a fixed-bed precipitator between the wells of the doublet. The FIG aquifer is highly layered and a really anisotropic. The upper Franconia and Ironton-Galesville parts of the aquifer, those parts screened, have hydraulic conductivities of {approximately}0.6 and {approximately}1.0 m/d, respectively. Primary ions in the ambient ground water are calcium and magnesium bicarbonate. Ambient temperature FIG ground water is saturated with respect to calcium/magnesium bicarbonate. Heating the ground water caused most of the dissolved calcium to precipitate out as calcium carbonate in the heat exchanger and precipitator. Silica, calcium, and magnesium were significantly higher in recovered water than in injected water, suggesting dissolution of some constituents of the aquifer during the cycles. Further work on the ground water chemistry is required to understand water-rock interactions.

Geochemical characterization and heavy metal migration in a coastal polluted aquifer incorporating tidal effects: field investigation in Chongming Island, China.

Science.gov (United States)

Liu, Shuguang; Tan, Bo; Dai, Chaomeng; Lou, Sha; Tao, An; Zhong, Guihui

2015-12-01

The occurrence and migration of heavy metal in coastal aquifer incorporating tidal effects were investigated in detail by the field geological survey and observation. The continuous groundwater sampling, field observation (for groundwater potentiometric surface elevation, pH, dissolved oxygen, temperature, and salinity), and laboratory analysis (for Cr, Ni, Cu, Zn, Cd, and Pb concentration) were conducted through eight monitoring wells located around the landfill in the northern part of Chongming Island, China. The results showed that the unconfined aquifer medium was estuary-littoral facies deposit of Holocene, mainly gray clayey silt and grey sandy silt, and the groundwater flow was mainly controlled by topography condition of the aquifer formation strike. The background values of Cr, Ni, Cu, Zn, Cd, and Pb in Chongming Island were 3.10 ± 3.09, 0.81 ± 0.25, 1.48 ± 1.09, 43.32 ± 33.06, 0.08 ± 0.16, and 0.88 ± 1.74 μg/L, respectively. Compared with the groundwater samples around the study area, the drinking water was qualified and was free from the seawater intrusion/estuarine facies contaminant encroachment. Pollutant discharge was reflected in water quality parameters, the Cr and Cu concentrations elevated to the peak of 50.07 and 46.00 μg/L, respectively, and meanwhile specific migration regularity was embodied in observation time series as well as other elements. This migration regularity was not fully identical according to correlations between these analyzed elements. Ambient watery environment, anthropogenic disturbance, regional hydrogeological condition, and biogeochemical reactivity on heavy metals reduced/altered the significance of elements correlation in the migration pathway in coastal aquifer.

Hydrogeologic and geochemical characterization and evaluation of two arroyos for managed aquifer recharge by surface infiltration in the Pojoaque River Basin, Santa Fe County, New Mexico, 2014–15

Science.gov (United States)

Robertson, Andrew J.; Cordova, Jeffrey; Teeple, Andrew; Payne, Jason; Carruth, Rob

2017-02-22

available for storage in the unconsolidated channel sands (about 410 acre-feet in the east arroyo and about 190 acre-feet in the west arroyo) and the potential for the infiltrating water to preferentially flow over the bedrock contact and out of the reach present a challenge for storing water. Although a detailed assessment of the infiltration rate of the Tesuque Formation is beyond the scope of this investigation, one double-ring infiltrometer test was conducted on an outcrop, resulting in an estimated infiltration rate of about 4 feet per day.The shallow groundwater observed in this investigation was determined to be recharged locally on the basis of groundwater elevations and geochemical and isotopic signatures. The channel sands and shallow bedrock were observed to be weathered, indicating contact with oxic groundwater following deposition. This observation was supported by whole-rock elemental analysis and mineralogy of several core samples. The downward groundwater gradient between the shallow wells and those wells screened at greater depths suggests that the shallow groundwater is recharged by local precipitation and has the potential to migrate to the deeper aquifer units. The two age-dating tracers measured in this investigation, however, demonstrate that the shallow groundwater flow paths are very slow and that the deeper flow paths are likely part of a larger regional system.The composition of the shallow, native groundwater suggests that storing water diverted from the Rio Grande is not likely to leach constituents of concern that would cause the stored water to exceed health-based U.S. Environmental Protection Agency Maximum Contaminant Levels.

Survival of bacterial indicators and the functional diversity of native microbial communities in the Floridan aquifer system, south Florida

Science.gov (United States)

Lisle, John T.

2014-01-01

The Upper Floridan aquifer in the southern region of Florida is a multi-use, regional scale aquifer that is used as a potable water source and as a repository for passively recharged untreated surface waters, and injected treated surface water and wastewater, industrial wastes, including those which contain greenhouse gases (for example, carbon dioxide). The presence of confined zones within the Floridan aquifer that range in salinity from fresh to brackish allow regulatory agencies to permit the injection of these different types of product waters into specific zones without detrimental effects to humans and terrestrial and aquatic ecosystems. The type of recharge that has received the most regulatory attention in south Florida is aquifer storage and recovery (ASR). The treated water, prior to injection and during recovery, must meet primary and secondary drinking water standards. The primary microbiology drinking water standard is total coliforms, which have been shown to be difficult to inactivate below the regulatory standard during the treatment process at some ASR facilities. The inefficient inactivation of this group of indicator bacteria permits their direct injection into the storage zones of the Floridan aquifer. Prior to this study, the inactivation rates for any member of the total coliform group during exposure to native geochemical conditions in groundwater from any zone of the Floridan aquifer had not been derived. Aboveground flow through mesocosms and diffusion chambers were used to quantify the inactivation rates of two bacterial indicators, Escherichia coli and Pseudomonas aeruginosa, during exposure to groundwater from six wells. These wells collect water from two ASR storage zones: the Upper Floridan aquifer (UFA) and Avon Park Permeable Zone (APPZ). Both bacterial strains followed a biphasic inactivation model. The E. coli populations had slower inactivation rates in the UFA (range: 0.217–0.628 per hour (h-1)) during the first phase of the

Nonstationary porosity evolution in mixing zone in coastal carbonate aquifer using an alternative modeling approach.

Science.gov (United States)

Laabidi, Ezzeddine; Bouhlila, Rachida

2015-07-01

In the last few decades, hydrogeochemical problems have benefited from the strong interest in numerical modeling. One of the most recognized hydrogeochemical problems is the dissolution of the calcite in the mixing zone below limestone coastal aquifer. In many works, this problem has been modeled using a coupling algorithm between a density-dependent flow model and a geochemical model. A related difficulty is that, because of the high nonlinearity of the coupled set of equations, high computational effort is needed. During calcite dissolution, an increase in permeability can be identified, which can induce an increase in the penetration of the seawater into the aquifer. The majority of the previous studies used a fully coupled reactive transport model in order to model such problem. Romanov and Dreybrodt (J Hydrol 329:661-673, 2006) have used an alternative approach to quantify the porosity evolution in mixing zone below coastal carbonate aquifer at steady state. This approach is based on the analytic solution presented by Phillips (1991) in his book Flow and Reactions in Permeable Rock, which shows that it is possible to decouple the complex set of equation. This equation is proportional to the square of the salinity gradient, which can be calculated using a density driven flow code and to the reaction rate that can be calculated using a geochemical code. In this work, this equation is used in nonstationary step-by-step regime. At each time step, the quantity of the dissolved calcite is quantified, the change of porosity is calculated, and the permeability is updated. The reaction rate, which is the second derivate of the calcium equilibrium concentration in the equation, is calculated using the PHREEQC code (Parkhurst and Apello 1999). This result is used in GEODENS (Bouhlila 1999; Bouhlila and Laabidi 2008) to calculate change of the porosity after calculating the salinity gradient. For the next time step, the same protocol is used but using the updated porosity

Geochemical and isotopic evidences for a severe anthropogenic boron contamination: A case study from Castelluccio (Arezzo, central Italy)

International Nuclear Information System (INIS)

Venturi, Stefania; Vaselli, Orlando; Tassi, Franco; Nisi, Barbara; Pennisi, Maddalena; Cabassi, Jacopo; Bicocchi, Gabriele; Rossato, Luca

2015-01-01

In 2009 a deterioration of garden plants watered with domestic wells was related to high boron concentrations (up to 57 mg/L) measured in the shallow aquifer from the industrial area of Castelluccio (Tuscany, Italy), where several factories are or were using boron compounds for their industrial processes. Since 2012 a geochemical and isotopic survey of stream, ground and waste waters, and sediment samples was performed. In addition, monthly geochemical surveys were carried out from January to September 2013, during which concentrations of boron up to 139 mg/L were measured. The geochemical dataset also included raw (borax and sodium boron-hydride) and anthropogenic materials (B-rich slags and muds stored in one of the local factories), the latter being, to the best of our knowledge, analyzed for the first time in this work for bulk and leachate boron concentration and isotopic ratios. The results highlighted that the high concentrations of boron found in the local shallow aquifer had unequivocally an anthropogenic source. It was suggested that prolonged interaction between industrial (presently stored at ground level or buried) by-products and waste and meteoric waters was likely the main process responsible of the groundwater contamination as supported by the analysis of the major solutes. The dispersion of the contaminant could not clearly be observed downward the shallow hydrogeological circuit. Consequently, the presence of other sources of boron in the industrial area of Castelluccio cannot be excluded. This would also explain the reason why no univocal results were obtained by the "1"1B/"1"0B isotopic ratios measured in water, sediment and (bulk and leachate) anthropogenic samples. To minimize the boron contamination a hydraulic barrier should be constructed where the highest concentrations of boron were measured. - Highlights: • High boron concentrations were measured in a groundwater system near Arezzo (Italy). • Several factories in the local

The Role of Science in Managed Aquifer Recharge--the Equus Beds aquifer near Wichita, Kansas Andrew Ziegler, Director Brian Kelly, Office Chief Michael Jacobs, Manager of Water Planning and Production Debra Ary, Engineer, Water Systems Planning (Invited)

Science.gov (United States)

Ziegler, A. C.; Jacobs, M.; Ary, D.; Kelly, B.

2013-12-01

Data collection and interpretation using statistical, geochemical, and numerical simulation tools are essential parts of a long-term cooperative study between the city of Wichita, U.S. Geological Survey, and others to describe water quantity and quality conditions in a 165 square-mile part of the Equus Beds aquifer and Arkansas and Little Arkansas Rivers. The Equus Beds aquifer, eastern part of the High Plains Aquifer in south-central Kansas, is a vital water resource for agriculture and city of Wichita. Withdrawals for public supply began in the 1940s and agricultural irrigation began in the 1950-60s. These withdrawals led to water-level declines of up to 40 feet (historic low in 1993), a storage loss of 250,000 acre feet compared to predevelopment, and may enhance movement of chloride contamination from a past oilfield disposal area near Burrton and from natural chloride along the Arkansas River. Monitoring data and modeling show chloride near Burrton moved about 3 miles in 45 years, is about 1 mile away from the nearest public supply wells, and will continue to move for decades to centuries making the water unusable for irrigation or water supply without treatment. These concerns led to development of Wichita's 1993 integrated local water-supply plan that increased use of Cheney Reservoir and implemented aquifer storage and recovery (ASR) within the aquifer using high flows from the Little Arkansas River. ASR benefits include replacing depleted storage and slowing chloride movement. Decreased withdrawals, increased precipitation, and artificial recharge increased water levels and added 100,000 acre feet of storage through 2010, but drought since 2011 has increased withdrawals. A calibrated model will be used to simulate transport of chloride under several withdrawal scenarios using MODFLOW coupled with SEAWAT. Since 1995, water-quality data collection for more than 400 organic and inorganic compounds in surface water, treated source water for artificial recharge

Study of variation in groundwater quality in a coastal aquifer in north-eastern Tunisia using multivariate factor analysis

KAUST Repository

Charfi, Sihem; Zouari, Kamel; Feki, Saber; Mami, Ezeddine

2013-01-01

This work focuses on the Grombalia aquifer which constitutes the main water resource in Northeast Tunisia, Cap Bon Peninsula. The recharge of this aquifer is ensured mainly by direct infiltration of rainwater through permeable layers. Under semi-arid climatic conditions and increasing water demand for irrigation, about 80% of the Grombalia aquifer system shows different vulnerabilities to anthropogenic activities. The total dissolved solids values range from 0.75 to 5.6g/l.Isotopic characterization with stable isotopes (δ2H and δ18O) of Grombalia aquifer system identified geochemistry processes that control water chemistry. In addition, the multivariate statistical technique (Principal Component Analysis) was used to identify the origin, the recharge mode and geochemical processes controlling groundwater quality. The principal reactions responsible for the hydrochemical evolution in the Grombalia groundwater fall into three categories: (1) denitrification process; (2) dissolution of salts; and (3) irrigation return flow process. Tritium data in groundwater from the study area suggest the existence of pre1950 and post1960 recharge. © 2012 Elsevier Ltd and INQUA.

Study of variation in groundwater quality in a coastal aquifer in north-eastern Tunisia using multivariate factor analysis

KAUST Repository

Charfi, Sihem

2013-07-01

This work focuses on the Grombalia aquifer which constitutes the main water resource in Northeast Tunisia, Cap Bon Peninsula. The recharge of this aquifer is ensured mainly by direct infiltration of rainwater through permeable layers. Under semi-arid climatic conditions and increasing water demand for irrigation, about 80% of the Grombalia aquifer system shows different vulnerabilities to anthropogenic activities. The total dissolved solids values range from 0.75 to 5.6g/l.Isotopic characterization with stable isotopes (δ2H and δ18O) of Grombalia aquifer system identified geochemistry processes that control water chemistry. In addition, the multivariate statistical technique (Principal Component Analysis) was used to identify the origin, the recharge mode and geochemical processes controlling groundwater quality. The principal reactions responsible for the hydrochemical evolution in the Grombalia groundwater fall into three categories: (1) denitrification process; (2) dissolution of salts; and (3) irrigation return flow process. Tritium data in groundwater from the study area suggest the existence of pre1950 and post1960 recharge. © 2012 Elsevier Ltd and INQUA.

Evaluation and development of hydrogeological and geochemical investigation methods for aquifers of low permeability

International Nuclear Information System (INIS)

Wijland, G.C.; Langemeijer, H.D.; Stapper, R.A.M.; Glasbergen, P.; Michelot, J.L.

1991-01-01

Studies are currently being carried out in the Netherlands to assess the environmental consequences of geological disposal of radioactive waste. In these studies transport models are used to evaluate the geohydrological system in formations overlying the potential host-rock, and to establish the potential pathways for radionuclides to the biosphere. Knowledge of parameter values, and of their variability for the investigated formations, is necessary to construct these models. From preceding work it became obvious that only a poor set of data is available, in particular for Paleogene and Upper Cretaceous deposits, that are present in the overburden of salt structures in the Netherlands. Within the current phase of the Netherlands programme on geological disposal it was considered essential to obtain an overview of methods and their accuracy which would be applicable for a geohydrological research programme first. From this work guidelines for the construction of new boreholes might also be derived. The main purposes of this study were defined as follows: to evaluate and to test techniques to obtain geohydrological data of the aquifers and aquitards of the Upper Cretaceous and Lower Tertiary formations. Also, geohydrochemical methods were evaluated and tested in order to find out whether they could contribute to the understanding of the groundwater flow system in aquifers of low permeability

Reactions and reaction rates in the regional aquifer beneath the Pajarito Plateau, north-central New Mexico, USA

Science.gov (United States)

Hereford, Anne G.; Keating, Elizabeth H.; Guthrie, George D.; Zhu, Chen

2007-05-01

Reactions and reaction rates within aquifers are fundamental components of critical hydrological processes. However, reactions simulated in laboratory experiments typically demonstrate rates that are much faster than those observed in the field. Therefore, it is necessary to conduct more reaction rate analyses in natural settings. This study of geochemical reactions in the regional aquifer in the Pajarito Plateau near Los Alamos, New Mexico combines modeling with petrographic assessment to further knowledge and understanding of complex natural hydrologic systems. Groundwater geochemistry shows marked evolution along assumed flow paths. The flow path chosen for this study was evaluated using inverse mass balance modeling to calculate the mass transfer. X-ray diffraction and field emission gun scanning electron microscopy were used to identify possible reactants and products. Considering the mineralogy of the aquifer and saturation indices for the regional water refined initial interpretations. Calculations yielded dissolution rates for plagioclase on the order of 10-15 mol s-1 m-2 and for K-feldspar on the order of 10-17 mol s-1 m-2, orders of magnitude slower than laboratory rates. While these rates agree with other aquifer studies, they must be considered in the light of the uncertainty associated with geometric surface area estimates, 14C ages, and aquifer properties.

Geochemical survey of an illegal waste disposal site under a waste emergency scenario (Northwest Naples, Italy).

Science.gov (United States)

Ferrara, L; Iannace, M; Patelli, A M; Arienzo, M

2013-03-01

Since the mid 1980s, Naples and the Campania region have suffered from the dumping of wastes into overfilled landfills. The aim was to characterise a former cave located in Roccarainola (Naples, Italy) for its eventual destination to a controlled landfill site. A detailed hydro-geochemical survey of the area was carried out through drilling of 14 boreholes and four monitoring wells. Samples of water, sediment and soil were analysed for heavy metals and organic contaminants from a dew pond placed in the middle of the cave. The underneath aquifer was also surveyed. The nature of gases emitted from the site was investigated. Results of the geognostic survey revealed the presence of huge volumes of composite wastes, approximately half a million of cubic metre, which accumulated up to a thickness of 25.6 m. In some points, wastes lie below the free surface level of the aquifer. The sampled material from the boreholes revealed levels of As, Cd, Cr, Cu, Hg, Pb, Sn, Tl and Zn exceeding the intervention legal limits. Outstanding loads of Cd, Pb and Zn were found, with levels exceeding of about 50, 100 and 1,870 times the limit. In several points, polycyclic aromatic hydrocarbon load was extremely high, 35 vs 1 mg kg(-1) of the threshold. The aquifer was also very heavily polluted by Cd, Cr-tot, Cu, Fe, Mn, Ni, Pb and Zn, with impressive high load of Cr and Mn, up to 250-370 times the limits. Hot gases up to 62 °C with presence of xylene and ethylbenzene were found. Results indicated that the site needs an urgent intervention of recovery to avoid compromising the surrounding areas and aquifers of the Campania plain.

Alaska Geochemical Database (AGDB)-Geochemical data for rock, sediment, soil, mineral, and concentrate sample media

Science.gov (United States)

Granitto, Matthew; Bailey, Elizabeth A.; Schmidt, Jeanine M.; Shew, Nora B.; Gamble, Bruce M.; Labay, Keith A.

2011-01-01

The Alaska Geochemical Database (AGDB) was created and designed to compile and integrate geochemical data from Alaska in order to facilitate geologic mapping, petrologic studies, mineral resource assessments, definition of geochemical baseline values and statistics, environmental impact assessments, and studies in medical geology. This Microsoft Access database serves as a data archive in support of present and future Alaskan geologic and geochemical projects, and contains data tables describing historical and new quantitative and qualitative geochemical analyses. The analytical results were determined by 85 laboratory and field analytical methods on 264,095 rock, sediment, soil, mineral and heavy-mineral concentrate samples. Most samples were collected by U.S. Geological Survey (USGS) personnel and analyzed in USGS laboratories or, under contracts, in commercial analytical laboratories. These data represent analyses of samples collected as part of various USGS programs and projects from 1962 to 2009. In addition, mineralogical data from 18,138 nonmagnetic heavy mineral concentrate samples are included in this database. The AGDB includes historical geochemical data originally archived in the USGS Rock Analysis Storage System (RASS) database, used from the mid-1960s through the late 1980s and the USGS PLUTO database used from the mid-1970s through the mid-1990s. All of these data are currently maintained in the Oracle-based National Geochemical Database (NGDB). Retrievals from the NGDB were used to generate most of the AGDB data set. These data were checked for accuracy regarding sample location, sample media type, and analytical methods used. This arduous process of reviewing, verifying and, where necessary, editing all USGS geochemical data resulted in a significantly improved Alaska geochemical dataset. USGS data that were not previously in the NGDB because the data predate the earliest USGS geochemical databases, or were once excluded for programmatic reasons

Methods for geochemical analysis

Science.gov (United States)

Baedecker, Philip A.

1987-01-01

The laboratories for analytical chemistry within the Geologic Division of the U.S. Geological Survey are administered by the Office of Mineral Resources. The laboratory analysts provide analytical support to those programs of the Geologic Division that require chemical information and conduct basic research in analytical and geochemical areas vital to the furtherance of Division program goals. Laboratories for research and geochemical analysis are maintained at the three major centers in Reston, Virginia, Denver, Colorado, and Menlo Park, California. The Division has an expertise in a broad spectrum of analytical techniques, and the analytical research is designed to advance the state of the art of existing techniques and to develop new methods of analysis in response to special problems in geochemical analysis. The geochemical research and analytical results are applied to the solution of fundamental geochemical problems relating to the origin of mineral deposits and fossil fuels, as well as to studies relating to the distribution of elements in varied geologic systems, the mechanisms by which they are transported, and their impact on the environment.

Assessing the efficiency of a coastal Managed Aquifer Recharge (MAR) system in Cyprus.

Science.gov (United States)

Tzoraki, Ourania; Dokou, Zoi; Christodoulou, George; Gaganis, Petros; Karatzas, George

2018-06-01

Managed Aquifer Recharge (MAR) is becoming an attractive water management option, with more than 223 sites operating in European countries. The quality of the produced water, available for drinking or irrigation processes is strongly depended on the aquifer's hydrogeochemical characteristics and on the MAR system design and operation. The objective of this project is the assessment of the operation efficiency of a MAR system in Cyprus. The coupling of alternative methodologies is used such as water quality monitoring, micro-scale sediment sorption experiments, simulation of groundwater flow and phosphate and copper transport in the subsurface using the FEFLOW model and evaluation of the observed change in the chemical composition of water due to mixing using the geochemical model PHREEQC. The above methodology is tested in the Ezousa MAR project in Cyprus, where treated effluent from the Paphos Waste Water Treatment Plant, is recharged into the aquifer through five sets of artificial ponds along the riverbed. Additionally, groundwater is pumped for irrigation purposes from wells located nearby. A slight attenuation of nutrients is observed, whereas copper in groundwater is overcoming the EPA standards. The FEFLOW simulations reveal no effective mixing in some intermediate infiltration ponds, which is validated by the inverse modeling simulation of the PHREEQC model. Based on the results, better control of the infiltration capacity of some of the ponds and increased travel times are some suggestions that could improve the efficiency of the system. Copyright © 2018 Elsevier B.V. All rights reserved.

Flow of river water into a Karstic limestone aquifer. 1. Tracing the young fraction in groundwater mixtures in the Upper Floridan Aquifer near Valdosta, Georgia

International Nuclear Information System (INIS)

Plummer, L.N.; Busenberg, E.; McConnell, J.B.; Drenkard, S.; Schlosser, P.; Michel, R.L.

1998-01-01

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 - , 3 H, tritiogenic helium-3 ( 3 He), chlorofluorocarbons (CFC-11, CFC-12, CFC-113), organic C (DOC), O 2 (DO), H 2 S, CH 4 , δ 18 O, δD, and 14 C 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 - , δ 18 O, δD, CFC-12, and the quantity ( 3 H+ 3 He) are stable in water from the Upper Floridan aquifer, whereas DOC, DO, H 2 S, CH 4 , 14 C, 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 δ 18 O data, recognizing 3 end-member water types in the groundwater mixtures: (1) Withlacoochee River water (δ 18 O=-2.5±0.3per thousand, Cl - =12.2±2 mg/l), (2) regional infiltration water (δ 18 O=-4.2±0.1per thousand, Cl - =2.3±0.1 mg/l), and (3) regional paleowater resident in the Upper Floridan aquifer (δ 18 O=-3.4±0.1per thousand, 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. (Copyright (c) 1998 Elsevier Science B.V., Amsterdam. All rights reserved.)

Flow of river water into a Karstic limestone aquifer. 1. Tracing the young fraction in groundwater mixtures in the Upper Floridan Aquifer near Valdosta, Georgia

Energy Technology Data Exchange (ETDEWEB)

Plummer, L.N.; Busenberg, E. [U.S. Geological Survey, 432 National Center, Reston, VA (United States); McConnell, J.B. [U.S. Geological Survey, 3039 Amwiler Rd., Atlanta, GA (United States); Drenkard, S.; Schlosser, P. [Lamont-Doherty Earth Observatory of Columbia University, 61 Route 9W, Palisades, NY (United States); Michel, R.L. [U.S. Geological Survey, Mail Stop 434, 345 Middlefield Road, Menlo Park, CA (United States)

1998-11-01

he 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{sup -}, {sup 3}H, tritiogenic helium-3 ({sup 3}He), chlorofluorocarbons (CFC-11, CFC-12, CFC-113), organic C (DOC), O{sub 2} (DO), H{sub 2}S, CH{sub 4}, {delta}{sup 18}O, {delta}D, and {sup 14}C 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{sup -}, {delta}{sup 18}O, {delta}D, CFC-12, and the quantity ({sup 3}H+{sup 3}He) are stable in water from the Upper Floridan aquifer, whereas DOC, DO, H{sub 2}S, CH{sub 4}, {sup 14}C, 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{sup -} and {delta}{sup 18}O data, recognizing 3 end-member water types in the groundwater mixtures: (1) Withlacoochee River water ({delta}{sup 18}O=-2.5{+-}0.3per thousand, Cl{sup -}=12.2{+-}2 mg/l), (2) regional infiltration water ({delta}{sup 18}O=-4.2{+-}0.1per thousand, Cl{sup -}=2.3{+-}0.1 mg/l), and (3) regional paleowater resident in the Upper Floridan aquifer ({delta}{sup 18}O=-3.4{+-}0.1per thousand, Cl{sup -}=2.6{+-}0.1 mg/l) (uncertainties are {+-}1{sigma}). 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 theN and NW of Valdosta, but becomes negligible to the S and SE in the direction of general thickening of post-Eocene confining

Geochemical computer codes. A review

International Nuclear Information System (INIS)

Andersson, K.

1987-01-01

In this report a review of available codes is performed and some code intercomparisons are also discussed. The number of codes treating natural waters (groundwater, lake water, sea water) is large. Most geochemical computer codes treat equilibrium conditions, although some codes with kinetic capability are available. A geochemical equilibrium model consists of a computer code, solving a set of equations by some numerical method and a data base, consisting of thermodynamic data required for the calculations. There are some codes which treat coupled geochemical and transport modeling. Some of these codes solve the equilibrium and transport equations simultaneously while other solve the equations separately from each other. The coupled codes require a large computer capacity and have thus as yet limited use. Three code intercomparisons have been found in literature. It may be concluded that there are many codes available for geochemical calculations but most of them require a user that us quite familiar with the code. The user also has to know the geochemical system in order to judge the reliability of the results. A high quality data base is necessary to obtain a reliable result. The best results may be expected for the major species of natural waters. For more complicated problems, including trace elements, precipitation/dissolution, adsorption, etc., the results seem to be less reliable. (With 44 refs.) (author)

Seasonal Deep Aquifer Thermal Energy Storage in the Gassum Sandstone Formation

DEFF Research Database (Denmark)

Holmslykke, H.D.H.; Kjøller, C.; Fabricius, Ida Lykke

Seasonal storage of excess heat in hot deep aquifers is considered to optimise the usage of commonly available energy sources. The potential chemical reactions caused by heating the Gassum Sandstone Formation to up to 150°C is investigated by core flooding experiments combined with petrographic...... analysis and geochemical modelling. Synthetic formation water is injected into two sets of Gassum Formation samples at 25°C, 50°C (reservoir temperature), 100°C and 150°C with a velocity of 0.05 PV/hr and 0.1 PV/hr, respectively. A significant increase in the aqueous concentration of silicium and iron...

Geochemical Implications of CO2 Leakage Associated with Geologic Storage: A Review

Energy Technology Data Exchange (ETDEWEB)

Harvey, Omar R.; Qafoku, Nikolla; Cantrell, Kirk J.; Brown, Christopher F.

2012-07-09

Leakage from deep storage reservoirs is a major risk factor associated with geologic sequestration of carbon dioxide (CO2). Different scientific theories exist concerning the potential implications of such leakage for near-surface environments. The authors of this report reviewed the current literature on how CO2 leakage (from storage reservoirs) would likely impact the geochemistry of near surface environments such as potable water aquifers and the vadose zone. Experimental and modeling studies highlighted the potential for both beneficial (e.g., CO2 re sequestration or contaminant immobilization) and deleterious (e.g., contaminant mobilization) consequences of CO2 intrusion in these systems. Current knowledge gaps, including the role of CO2-induced changes in redox conditions, the influence of CO2 influx rate, gas composition, organic matter content and microorganisms are discussed in terms of their potential influence on pertinent geochemical processes and the potential for beneficial or deleterious outcomes. Geochemical modeling was used to systematically highlight why closing these knowledge gaps are pivotal. A framework for studying and assessing consequences associated with each factor is also presented in Section 5.6.

Evaluation of processes controlling the geochemical constituents in deep groundwater in Bangladesh: Spatial variability on arsenic and boron enrichment

International Nuclear Information System (INIS)

Halim, M.A.; Majumder, R.K.; Nessa, S.A.; Hiroshiro, Y.; Sasaki, K.; Saha, B.B.; Saepuloh, A.; Jinno, K.

2010-01-01

Forty-six deep groundwater samples from highly arsenic affected areas in Bangladesh were analyzed in order to evaluate the processes controlling geochemical constituents in the deep aquifer system. Spatial trends of solutes, geochemical modeling and principal component analysis indicate that carbonate dissolution, silicate weathering and ion exchange control the major-ion chemistry. The groundwater is dominantly of Na-Cl type brackish water. Approximately 17% of the examined groundwaters exhibit As concentrations higher than the maximum acceptable limit of 10 μg/L for drinking water. Strong correlation (R 2 = 0.67) of Fe with dissolved organic carbon (DOC) and positive saturation index of siderite suggests that the reductive dissolution of Fe-oxyhydroxide in presence of organic matter is considered to be the dominant process to release high content of Fe (median 0.31 mg/L) in the deep aquifer. In contrast, As is not correlated with Fe and DOC. Boron concentration in the 26% samples exceeds the standard limit of 500 μg/L, for water intended for human consumption. Negative relationships of B/Cl ratio with Cl and boron with Na/Ca ratio demonstrate the boron in deep groundwater is accompanied by brackish water and cation exchange within the clayey sediments.

Surface complexation modeling of groundwater arsenic mobility: Results of a forced gradient experiment in a Red River flood plain aquifer, Vietnam

Science.gov (United States)

Jessen, Søren; Postma, Dieke; Larsen, Flemming; Nhan, Pham Quy; Hoa, Le Quynh; Trang, Pham Thi Kim; Long, Tran Vu; Viet, Pham Hung; Jakobsen, Rasmus

2012-12-01

Three surface complexation models (SCMs) developed for, respectively, ferrihydrite, goethite and sorption data for a Pleistocene oxidized aquifer sediment from Bangladesh were used to explore the effect of multicomponent adsorption processes on As mobility in a reduced Holocene floodplain aquifer along the Red River, Vietnam. The SCMs for ferrihydrite and goethite yielded very different results. The ferrihydrite SCM favors As(III) over As(V) and has carbonate and silica species as the main competitors for surface sites. In contrast, the goethite SCM has a greater affinity for As(V) over As(III) while PO43- and Fe(II) form the predominant surface species. The SCM for Pleistocene aquifer sediment resembles most the goethite SCM but shows more Si sorption. Compiled As(III) adsorption data for Holocene sediment was also well described by the SCM determined for Pleistocene aquifer sediment, suggesting a comparable As(III) affinity of Holocene and Pleistocene aquifer sediments. A forced gradient field experiment was conducted in a bank aquifer adjacent to a tributary channel to the Red River, and the passage in the aquifer of mixed groundwater containing up to 74% channel water was observed. The concentrations of As (SCM correctly predicts desorption for As(III) but for Si and PO43- it predicts an increased adsorption instead of desorption. The goethite SCM correctly predicts desorption of both As(III) and PO43- but failed in the prediction of Si desorption. These results indicate that the prediction of As mobility, by using SCMs for synthetic Fe-oxides, will be strongly dependent on the model chosen. The SCM based on the Pleistocene aquifer sediment predicts the desorption of As(III), PO43- and Si quite superiorly, as compared to the SCMs for ferrihydrite and goethite, even though Si desorption is still somewhat under-predicted. The observation that a SCM calibrated on a different sediment can predict our field results so well suggests that sediment based SCMs may be a

Hydrological connectivity of perched aquifers and regional aquifers in semi-arid environments: a case study from Namibia

Science.gov (United States)

Hamutoko, J. T.; Wanke, H.

2017-12-01

Integrated isotopic and hydrological tracers along with standard hydrological data are used to understand complex dry land hydrological processes on different spatial and temporal scales. The objective of this study is to analyse the relationship between the perched aquifers and the regional aquifer using hydrochemical data and isotopic composition in the Cuvelai-Etosha Basin in Namibia. This relation between the aquifers will aid in understanding groundwater recharge processes and flow dynamics. Perched aquifers are discontinuous shallow aquifers with water level ranging from 0 to 30 meters below ground level. The regional aquifer occurs in semi-consolidated sandstone at depths between about 60 and 160 meters below ground level. Water samples were collected from both aquifers in 10 villages and were analysed for major ions and stable isotopes. The results show overlapping hydrochemistry and isotopic compositions of both aquifers in 8 villages which suggest the possibility of perched aquifer water infiltrating into the regional aquifer. In two villages the hydrochemistry and isotopic composition of the aquifers are totally different and this suggests that there is no interaction between this aquifers. Areas where perched aquifers are connected to regional aquifers maybe recharge zones. These finding have important implications for groundwater resource management.

Towards sustainable groundwater management in Karst aquifers in semi-arid environments: Central West Bank, Palestine

Science.gov (United States)

Jebreen, H.; Banning, A.; Wohnlich, S.

2017-12-01

The Central West Bank (CWB) is characterized by karstified carbonate aquifers in the semiarid climate zone, where groundwater resources are frequently threatened by overexploitation and pollution. Despite often limited system knowledge, quantitative and qualitative factors such as groundwater recharge rate, aquifer parameters, flow and transport dynamics, anthropogenic impacts, and groundwater vulnerability need to be assessed. Therefore, sustainable groundwater use in the CWB is of critical importance. In the present study, we explore the scale of the groundwater problems in CWB as well as the possibility of sustainable management through different scenarios: 1) Managed aquifer recharge using a water balance model, stable isotopes (2H & 18O) and chloride mass balance, 2) Geochemical evolution and renewability of groundwater, and 3) Anthropogenic impacts. A total of 20 spring water samples were collected and analyzed for pH, electrical conductivity, total dissolved solids (TDS), hardness, major-ion chemistry (Cl-, HCO3-, SO42-, Na+, K+, Ca2+ and Mg2+), trace elements (Li, Be, Al, Ba, Tl, Pb, Bi, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Rb, Sr, Mo, Ag and Cd), microbiological data (total and fecal coliforms bacteria), and stable isotopes (2H & 18O). The results show a spatialized recharge rate, which ranges from 111-211 mm/year, representing 17-33 % of the long-term mean annual rainfall. The mean annual actual evapotranspiration was about 19-37 % of precipitation. The chemical composition of groundwater of the study area is strongly influenced by rock-water interaction, dissolution and deposition of carbonate and silicate minerals. Stable isotopes show that precipitation is the source of recharge to the groundwater system. All analyzed spring waters are suitable for irrigation but not for drinking purposes. This studýs results can serve as a basis for decision makers, and will lead to an increased understanding of the sustainable management of the Central West Bank

Hydrology of the Claiborne aquifer and interconnection with the Upper Floridan aquifer in southwest Georgia

Science.gov (United States)

Gordon, Debbie W.; Gonthier, Gerard

2017-04-24

The U.S. Geological Survey conducted a study, in cooperation with the Georgia Environmental Protection Division, to define the hydrologic properties of the Claiborne aquifer and evaluate its connection with the Upper Floridan aquifer in southwest Georgia. The effort involved collecting and compiling hydrologic data from the aquifer in subarea 4 of southwestern Georgia. Data collected for this study include borehole geophysical logs in 7 wells, and two 72-hour aquifer tests to determine aquifer properties.The top of the Claiborne aquifer extends from an altitude of about 200 feet above the North American Vertical Datum of 1988 (NAVD 88) in Terrell County to 402 feet below NAVD 88 in Decatur County, Georgia. The base of the aquifer extends from an altitude of about 60 feet above NAVD 88 in eastern Sumter County to about 750 feet below NAVD 88 in Decatur County. Aquifer thickness ranges from about 70 feet in eastern Early County to 400 feet in Decatur County.The transmissivity of the Claiborne aquifer, determined from two 72-hour aquifer tests, was estimated to be 1,500 and 700 feet squared per day in Mitchell and Early Counties, respectively. The storage coefficient was estimated to be 0.0006 and 0.0004 for the same sites, respectively. Aquifer test data from Mitchell County indicate a small amount of leakage occurred during the test. Groundwater-flow models suggest that the source of the leakage was the underlying Clayton aquifer, which produced about 2.5 feet of drawdown in response to pumping in the Claiborne aquifer. The vertical hydraulic conductivity of the confining unit between the Claiborne and Clayton aquifers was simulated to be about 0.02 foot per day.Results from the 72-hour aquifer tests run for this study indicated no interconnection between the Claiborne and overlying Upper Floridan aquifers at the two test sites. Additional data are needed to monitor the effects that increased withdrawals from the Claiborne aquifer may have on future water resources.

Geochemical alteration vs mechanical weathering on stability of unstable slope : Case of the deep seated landslide of Séchilienne (Isère, France)

Science.gov (United States)

Bertrand, Catherine; Nevers, Pierre; Gaillardet, Jérôme; Dubois, Laurent

2017-04-01

The Séchilienne landslide is located on the right bank of the Romanche River, South East of Grenoble (Isère, France). The active zone of the gravitational instability involves several millions of cubic meters. The geology consists of fractured hard rocks (micaschists) with double permeability and strong spatial heterogeneities. The permeability of the basement areas is rather obtained by long term weathering, which can be associated with a mechanical action in high relief mountainous regions. Water plays two major roles, the first one being a hydrogeological process, which is a factor that worsens instability, and the second one being a geochemical factor that alters the massif, making it less cohesive. These two factors interact through time and modify permeability and therefore the flow of water within the rock. Hydrochemistry simultaneously provides information about water flows (location and amount of refill, types and flow patterns, storage, residence time), and also about the acquisition of the chemistry during its transit through the aquifer (water-rock interaction during the transit, quantification of the alteration). The issue is to improve the knowledge of the genesis of the chemical signal, and to define the contributions of the knowledge of this signal in terms of functioning, on the pressure transferring as well as on the mass transferring and its effects. Hydrogeochemistry, which is integrative of the entire "history" of the water in the different compartments, paired with geochemical modelling, which allow the discrimination of the chemical signal according to its path in the aquifer, turns out to be an appropriate method for the objective. These tools (hydrogeochemistry & geochemical modelling) are designed to understand the complex relationship between chemical weathering, hydromechanical changes and weakening / deformation of the unstable rock slope The deformation of the unstable slope is monitored by on-site extensometric gauges, inclinometers

Uruguay mining inventory. Geochemical prospecting results of the Amarillo aerial map

International Nuclear Information System (INIS)

Zeegers, H.; Spangenberg, J.

1981-01-01

This report is about the results of the geochemical prospection carried out on the Amarillo aerial map, it placed in the area 24 of Uruguay (G11 section).This prospection was carried out by Geologic Institute team of Uruguay (IGU) with the technical assistance of BRGM. The Amarillo aerial map covers parts of Isla Cristalina. This is the window of the insular precrambrian shelf and it is surounded by geological formation as paleozoic and other more reecently formations too. The precambrian formation are represented by three big whole groups: metamorphic serial; groups of intrusing granites; and metamorphic rocks

Application of the top specified boundary layer (TSBL) approximation to initial characterization of an inland aquifer mineralization: 2. Seepage of saltwater through semi-confining layers

Science.gov (United States)

Rubin, H.; Buddemeier, R.W.

1998-01-01

This paper presents a generalized basic study that addresses practical needs for an understanding of the major mechanisms involved in the mineralization of groundwater in the Great Bend Prairie aquifer in south- central Kansas. This Quaternary alluvial aquifer and associated surface waters are subject to contamination by saltwater, which in some areas seeps from the deeper Permian bedrock formation into the overlying freshwater aquifer through semiconfining layers. A simplified conceptual model is adopted. It incorporates the freshwater aquifer whose bottom is comprised of a semiconfining layer through which a hydrologically minor but geochemically important saline water discharge seeps into the aquifer. A hierarchy of approximate approaches is considered to analyze the mineralization processes taking place in the aquifer. The recently developed top specified boundary layer (TSBL) approach is very convenient to use for the initial characterization of these processes, and is further adapted to characterization of head-driven seepage through semi-confining layers. TSBL calculations indicate that the seeping saline water may create two distinct new zones in the aquifer: (1) a completely saline zone (CSZ) adjacent to the semiconfining bottom of the aquifer, and (2) a transition zone (TZ) which develops between the CSZ and the freshwater zone. Some possible scenarios associated with the various mineralization patterns are analyzed and discussed.

Considerations in the extraction of uranium from a fresh-water aquifer - Miocene Oakville Sandstone, south Texas

International Nuclear Information System (INIS)

Henry, C.D.; Galloway, W.E.; Smith, G.E.

1982-01-01

The Miocene Oakville Sandstone is a major aquifer and uranium host beneath the Texas Coastal Plain. Present and future uranium mining by either surface or in situ methods could affect the availability and quality of Oakville ground water unless the mining is designed properly. Possible effects of mining, potential natural mitigation of these effects, and approaches to minimizing the impact of mining on the aquifer system are discussed. Both solution and surface mining may affect the availability of ground water by altering recharge characteristics and permeability. Because the volume of the aquifer affected by mining is small compared with its total volume, availability of Oakville ground water will probably not be reduced significantly, except in wells immediately adjacent to a mine. Mining may affect the quality of ground water by introducing chemicals that are not indigenous to the aquifer or by inducing chemical reactions that do not occur naturally or that occur at much slower rates. Most mining companies no longer use concentrated, ammonium-based leaches because of known problems in restoring water to its original chemistry. Natural and induced release of trace elements such as molybdenum is known to occur, but the geochemical controls on mobility and potential mitigating reactions in the aquifer are poorly understood. Because the affected aquifer volume is small, any deterioration of water quality will probably be localized. Observations and recommendations are presented on: regional and local baseline studies, determination of aquifer sensitivity, methods and goals of monitoring during and after mining, and need for research on poorly understood aspects of mining impact. Such impacts include chemical reactions and processes that affect the long-term release of trace elements

Impact of pH on hydrogen oxidizing redox processes in aquifers due to gas intrusions

Science.gov (United States)

Metzgen, Adrian; Berta, Marton; Dethlefsen, Frank; Ebert, Markus; Dahmke, Andreas

2017-04-01

(first order rate constants between 0.029 and 0.036 1/h). Between pH 7 and 8, acetogenesis showed a linear trend (zeroth order rates between 3 and 5 µM/h) whereas formate production became the main process (zeroth order rates between 38 to 197 µM/h) together with methanogenesis as a minor process. The results indicated a strong dependency of the biogeochemical hydrogenotrophic redox reactions on the pH milieu. Thus, pH buffers such as dissolved or solid phase carbonates should be taken into account when predicting effects a hydrogen leakage may have on shallow aquifers. Additionally, parameters derived from the observed processes and their rates allow the design of a process based numerical model simulating a hydrogen intrusion into a shallow aquifer. Consequently the presented outcomes allow an exemplary quantification of the resulting geochemical effects. This study was carried out within the ANGUS+ project and was funded by the German Federal Ministry of Education and Research (BMBF) energy storage funding initiative.

Estimating energy fluxes within the stream-aquifer interface of the Avenelles basin

Science.gov (United States)

Berrhouma, Asma; Rivière, Agnès; Goblet, Patrick; Cucchi, Karina; Rubin, Yoram; Baudin, Aurélien; Ansart, Patrick; Flipo, Nicolas

2017-04-01

The understanding of water temperature evolution and its associated energy fluxes is important to follow the aquatic habitats evolution and to predict future modifications induced by climate change. The spatio-temporal energy balance dynamics within the stream-aquifer interface is complex because of the multitude of physical, morphological and meteorological parameters on which it depends. This critical interface is involving numerous physical and bio-geochemical processes which are taking place at different time and spatial scales. The energy balance estimation at this interface depends mainly on the direction, magnitude and variability of water exchanges and the temporal variation of river and aquifer temperatures as well as the thermal porous media properties. In this work, a combined numerical and experimental approach is used to study the temporal and spatial evolution of the energy budget along 6 km of the stream network of the Avenelles watershed. With an area of 46 km2, the Avenelles watershed is located 70 km east from Paris. The Avenelles river presents different types of connectivity with the underlying aquifers. Five Local Monitoring Stations (LOMOS) have been deployed along the hydraulic corridor to monitor the water and thermal exchanges between the stream and aquifer over years, based on continuous pressure and temperature measurements in the river, the hyporheic zone (HZ) and the underlying aquifer. A 2D finite element thermo-hydrogeological model (METIS) coupled with a parameters screening script is used to determine the hydrogeological and thermal properties of the HZ and of the underlying aquifers by inversion at five LOMOS. Once the local models are calibrated, water and heat fluxes through the stream - aquifer interface are assessed over years (2012-2015) along the stream network. This work offers a new understanding of the stream-aquifer interface functioning, shifting from a pure hydrological characterizing toward a more subtle view that

Role of Dissolved Organic Matter and Geochemical Controls on Arsenic Cycling from Sediments to Groundwater along the Meghna River, Bangladesh: Tracking possible links to permeable natural reactive barrier

Science.gov (United States)

Datta, S.; Berube, M.; Knappett, P.; Kulkarni, H. V.; Vega, M.; Jewell, K.; Myers, K.

2017-12-01

Elevated levels of dissolved arsenic (As), iron (Fe) and manganese (Mn) are seen in the shallow groundwaters of southeast Bangladesh on the Ganges Brahmaputra Meghna River delta. This study takes a multi disciplinary approach to understand the extent of the natural reactive barrier (NRB) along the Meghna River and evaluate the role of the NRB in As sequestration and release in groundwater aquifers. Shallow sediment cores, and groundwater and river water samples were collected from the east and west banks of the Meghna. Groundwater and river water samples were tested for FeT, MnT, and AsT concentrations. Fluorescence spectroscopic characterization of groundwater dissolved organic matter (DOM) provided insight into the hydro geochemical reactions active in the groundwater and the hyporheic zones. Eight sediment cores of 1.5 m depth were collected 10 m away from the edge of the river. Vertical solid phase concentration profiles of Fe, Mn and As were measured via 1.2 M HCl digestion which revealed solid phase As accumulation along the riverbanks up to concentrations of 1500 mg/kg As. Microbial interactions with DOM prompts the reduction of Fe3+ to Fe2+, causing As to mobilize into groundwater and humic-like DOM present in the groundwater may catalyze this process. The extent to which microbially mediated release of As occurs is limited by labile dissolved organic carbon (DOC) availability. Aqueous geochemical results showed the highest dissolved As concentrations in shallow wells (groundwater was found to contain microbial and terrestrial derived DOC, and decomposed, humified and aromatic DOM. Deeper aquifers had a significantly larger microbial OM signature than the shallower aquifers and was less aromatic, decomposed and humified. The results from this study illustrate the potential for humic substances to contribute to As cycling and quantify the extent of As accumulation in the sediments and groundwater along a 1 km stretch of the Meghna. These findings contribute

Evaluating the rate of migration of an uranium deposition front within the Uitenhage Aquifer

CSIR Research Space (South Africa)

Vogel

1999-07-01

Full Text Available of Geochemical Exploration 66 (1999) 269?276 www.elsevier.com/locate/jgeoexp Evaluating the rate of migration of an uranium deposition front within the Uitenhage Aquifer J.C. Vogel a,A.S.Talmaa, T.H.E. Heaton b, J. Kronfeld c,* a Quaternary Dating Research Unit... stream_source_info vogel_1999.pdf.txt stream_content_type text/plain stream_size 18078 Content-Encoding ISO-8859-1 stream_name vogel_1999.pdf.txt Content-Type text/plain; charset=ISO-8859-1 ELSEVIER Journal...

Trends and transformation of nutrients and pesticides in a Coastal Plain aquifer system, United States

Science.gov (United States)

Denver, J.M.; Tesoriero, A.J.; Barbaro, J.R.

2010-01-01

Four local-scale sites in areas with similar corn (Zea mays L.) and soybean [Glycine max (L.) Merr.] agriculture were studied to determine the effects of different hydrogeologic settings of the Northern Atlantic Coastal Plain (NACP) on the transport of nutrients and pesticides in groundwater. Settings ranged from predominantly well-drained soils overlying thick, sandy surficial aquifers to predominantly poorly drained soils with complex aquifer stratigraphy and high organic matter content. Apparent age of groundwater, dissolved gases, N isotopes, major ions, selected pesticides and degradates, and geochemical environments in groundwater were studied. Agricultural chemicals were the source of most dissolved ions in groundwater. Specific conductance was strongly correlated with reconstructed nitrate (the sum of N in nitrate and N gas) (R2 = 0.81, p < 0.0001), and is indicative of the relative degree of agricultural effects on groundwater. Trends in nitrate were primarily related to changes in manure and fertilizer use at the well-drained sites where aquifer conditions were consistently oxic. Nitrate was present in young groundwater but completely removed over time through denitrification at the poorly drained sites where there were variations in chemical input and in geochemical environment. Median concentrations of atrazine (6-chloro-N-ethyl-N'-(1- methylethyl)-1,3,5-triazine-2,4-diamine), metolachlor (2-chloro-N-(2-ethyl-6- methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide), and some of their common degradates were higher at well-drained sites than at poorly drained sites, with concentrations of degradates generally higher than those of the parent compounds at all sites. An increase in the percentage of deethylatrazine to total atrazine over time at one well-drained site may be related to changes in manure application. Copyright ?? 2010 by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America. All rights reserved.

Observation of a Distinct Transition in Transport Response to Injection Stress in the Floridan Aquifer System, Southeastern Florida, U.S.A

Science.gov (United States)

King, J. N.; Cunningham, K. J.; Foster, A. L.

2011-12-01

The Miami-Dade Water and Sewer Department (MDWASD) injects effluent approximately one km below land surface into the Boulder Zone (BZ) at the North District Wastewater Treatment Plant (NDWWTP). The BZ is highly conductive and composed of fractured dolomite. MDWASD monitors upward effluent migration 450 m below land surface in the Avon Park Permeable Zone (APPZ). The BZ and APPZ---units within the Floridan aquifer system---are separated by a series of inter-bedded aquifers and leaky confining units with hydraulic conductivities that are orders of magnitude smaller than the BZ. MDWASD injected effluent at the NDWWTP during two distinct periods: (1) July 1997 to September 1999, and (2) August 2004 to January 2011. No effluent was injected between October 1999 and July 2004. A few months after the July 1997 injection, MDWASD observed effluent constituents in the APPZ (Figure 1). Some confinement bypass feature permits effluent constituents to be transported from the BZ to the APPZ. Bypass features may include poorly-cased wells, or natural conduits such as fractures, faults, or karst collapse systems. It is possible to describe confinement bypass features with conductance KA/L, where K is hydraulic conductivity, A is cross-sectional area, and L is length. MDWASD observed a distinct transition in the transport response to injection stress of total dissolved solids (TDS) concentration in the APPZ. The conductance required to describe early system response (1997-1999) is one order-of-magnitude larger than the conductance required to describe late system response (2004-2011). Hypotheses to explain transient conductance include clogging of bypass features by some geochemical or biological process that results from the mixing of effluent with groundwater; dissolution or precipitation; or changes in bypass-feature geometry forced by cyclical changes in aquifer-fluid pressure associated with injection. Hypotheses may be tested with geochemical analyses, tracer tests, hydraulic

Hydro geochemistry and isotopic approach of coastal aquifer systems of Cap Bon : The case of tablecloths and the eastern coast of El Haourai - Tunisia

International Nuclear Information System (INIS)

Ben Hammouda, Fethi

2008-01-01

As many other semi-arid regions, the Cap Bon peninsula (N.E. Tunisia) shows a parallel increase in overexploitation and mineralization of groundwater resources. In the eastern coast and El Haouaria aquifers, the groundwater quality is threatened. Surveys including level measurements, water sampling, chemical analysis (ions Na+, Cl., Ca2+, Mg2+, Br.) and sotopes (18O, 2H, 3H, 13C, 14C) were performed in 2001, 2002 and 2003. Several analysis types were conducted and results are compared with the hydrodynamic information for identifying the main processes involved in the mineralization increase. Particularly, the isotopes were permitting the understanding of the hydrogeological of the concerned aquifers and the localization of the recharge zones. Because the regional situation along the seashore, the seawater intrusion in the unconfined Plio-quaternary aquifer, resulting from the groundwater overexploitation, and obvious explanation for the rising salinity is identified but is not the only cause of the qualitative degradation: the irrigation development that induces the soil leaching and the fertilizers transfer to groundwater over the whole aquifer extent is another major reason of the mineralization increase. Piezometric and salinity maps of the Plio-quaternary aquifer were established. The continuous increase in pumping has created several depressions in the water table, up to 12 m below msl and induced a deterioration of the water quality. The temporal changes in water-table level and salinity are often similar which suggests a strong link between them. Several geochemical approaches were performed to identify the importance of the marine intrusion in the increase in mineralization. The salinity of the groundwater appears to originate from dissolution of minerals in the aquifer system

Hydrological and geochemical constraints on the mechanism of formation of arsenic contaminated groundwater in Sonargaon, Bangladesh

Energy Technology Data Exchange (ETDEWEB)

Itai, Takaaki [Institute for Study of the Earth' s Interior, Okayama University, Misasa, Tottori 682-0193 (Japan)], E-mail: itai-epss@hiroshima-u.ac.jp; Masuda, Harue [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Seddique, Ashraf A. [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Department of Geology, University of Dhaka, Dhaka 1000 (Bangladesh); Mitamura, Muneki [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Maruoka, Teruyuki [Department of Integrative Environmental Science, University of Tsukuba, Tsukuba, Ibaraki 305-8572 (Japan); Li, Xiaodong [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Kusakabe, Minoru [Institute for Study of the Earth' s Interior, Okayama University, Misasa, Tottori 682-0193 (Japan); Dipak, Biswas K. [Department of Geology, University of Dhaka, Dhaka 1000 (Bangladesh); Farooqi, Abida [Department of Geosciences, Osaka-City University, Sugimoto-tyo, Sumiyoshi, Osaka 558-8585 (Japan); Yamanaka, Toshiro [Department of Earth Systems Science, Okayama University, 3-1-1 Tsushima-naka Okayama 700-8530 (Japan); Nakaya, Shinji [Department of Civil Engineering, Shinshu University, Wakazato, Nagano 380-8553 (Japan); Matsuda, Jun-ichi [Department of Earth and Space Science, Osaka University, 1-1 Machikaneyama-tyo, Toyonaka-shi, Osaka 560-0043 (Japan); Ahmed, Kazi Matin [Department of Geology, University of Dhaka, Dhaka 1000 (Bangladesh)

2008-11-15

The geochemical characteristics and hydrological constraints of high As groundwater in Sonargaon, in mid-eastern Bangladesh were investigated in order to ascertain the mechanism of As release into the groundwaters from host sediments in the Ganges-Brahmaputra delta. Samples of groundwater were collected from ca. 230 tube wells in both the rainy and dry seasons. Similar to previous studies, high As groundwater was found in the Holocene unconfined aquifer but not in the Pleistocene aquifer. Groundwaters in the Holocene aquifer were of the Ca-Mg-HCO{sub 3} type with major solutes derived from chemical weathering of detrital minerals such as plagioclase and biotite. Groundwater with high As was generally characterized by high NH{sub 4}{sup +}, possibly derived from the agricultural application of fertilizer as suggested by the small variation of {delta}{sup 15}N{sub NH4} (mostly 2-4 per mille ). Concentrations of Fe changed between the rainy and dry seasons by precipitation/dissolution of Fe oxyhydroxide and siderite, whilst there was not an apparent concomitant change in As. Inhomogeneous spatial distribution of {delta}{sup 18}O in the Holocene unconfined aquifer indicates poor mixing of groundwater in the horizontal direction. Spatial variation of redox conditions is associated with localized variations in subsurface permeability and the recharge/discharge cycle of groundwater. Hydrogeochemical data presented in this paper suggest that reduction of Fe oxyhydroxide is not the only mechanism of As mobilization, and chemical weathering of biotite and/or other basic minerals in the Holocene aquifer could also be important as a primary cause of As mobilization.

Arsenic mobilization in an alluvial aquifer of the Terai region, Nepal

Directory of Open Access Journals (Sweden)

Jasmine Diwakar

2015-09-01

New Hydrological Insights for the Region: The aquifer is characterized by Ca-HCO3 type water and is multi-contaminated, with the WHO guideline values exceeded for As, Mn and F in 80%, 70% and 40% of cases respectively. The middle portion of the floodplain was heavily contaminated with As, predominantly as As(III. The river water displayed some evidence of reductive processes in the hyporheic zone contributing As, Fe and Mn to baseflow and also had elevated fluoride. The generally sub-oxic conditions, dominance of As(III and Fe2+ species and positive correlation between As and both NH3 and UV-absorbance at 254 nm suggests that oxidation of organic matter coupled with microbial mediated reductive processes are important for mobilizing As in the aquifer. The apparent decoupling between As(III(aq and Fe2+(aq may be explained by precipitation of siderite, but further work is required to resolve this unambiguously. Along with reductive processes, other geochemical mechanisms including silicate weathering and precipitation/dissolution of carbonate minerals, control the solute and major ion composition of groundwater.

Geochemical controls on the composition of soil pore waters beneath a mixed waste disposal site in the unsaturated zone

International Nuclear Information System (INIS)

Rawson, S.A.; Hubbell, J.M.

1989-01-01

Soil pore waters are collected routinely to monitor a thick unsaturated zone that separates a mixed waste disposal site containing transuranic and low-level radioactive wastes from the Snake River Plain aquifer. The chemistry of the soil pore waters has been studied to evaluate the possible control on the water composition by mineral equilibria and determine the extent, if any, of migration of radionuclides from the disposal site. Geochemical codes were used to perform speciation calculations for the waters. The results of speciation calculations suggest that the installation of the lysimeters affects the observed silica contents of the soil pore waters. The results also establish those chemical parameters that are controlled by secondary mineral precipitation. 15 refs., 6 figs., 1 tab

A General Solution for Groundwater Flow in Estuarine Leaky Aquifer System with Considering Aquifer Anisotropy

Science.gov (United States)

Chen, Po-Chia; Chuang, Mo-Hsiung; Tan, Yih-Chi

2014-05-01

In recent years the urban and industrial developments near the coastal area are rapid and therefore the associated population grows dramatically. More and more water demand for human activities, agriculture irrigation, and aquaculture relies on heavy pumping in coastal area. The decline of groundwater table may result in the problems of seawater intrusion and/or land subsidence. Since the 1950s, numerous studies focused on the effect of tidal fluctuation on the groundwater flow in the coastal area. Many studies concentrated on the developments of one-dimensional (1D) and two-dimensional (2D) analytical solutions describing the tide-induced head fluctuations. For example, Jacob (1950) derived an analytical solution of 1D groundwater flow in a confined aquifer with a boundary condition subject to sinusoidal oscillation. Jiao and Tang (1999) derived a 1D analytical solution of a leaky confined aquifer by considered a constant groundwater head in the overlying unconfined aquifer. Jeng et al. (2002) studied the tidal propagation in a coupled unconfined and confined costal aquifer system. Sun (1997) presented a 2D solution for groundwater response to tidal loading in an estuary. Tang and Jiao (2001) derived a 2D analytical solution in a leaky confined aquifer system near open tidal water. This study aims at developing a general analytical solution describing the head fluctuations in a 2D estuarine aquifer system consisted of an unconfined aquifer, a confined aquifer, and an aquitard between them. Both the confined and unconfined aquifers are considered to be anisotropic. The predicted head fluctuations from this solution will compare with the simulation results from the MODFLOW program. In addition, the solutions mentioned above will be shown to be special cases of the present solution. Some hypothetical cases regarding the head fluctuation in costal aquifers will be made to investigate the dynamic effects of water table fluctuation, hydrogeological conditions, and

Carbonate aquifers

Science.gov (United States)

Cunningham, Kevin J.; Sukop, Michael; Curran, H. Allen

2012-01-01

Only limited hydrogeological research has been conducted using ichnology in carbonate aquifer characterization. Regardless, important applications of ichnology to carbonate aquifer characterization include its use to distinguish and delineate depositional cycles, correlate mappable biogenically altered surfaces, identify zones of preferential groundwater flow and paleogroundwater flow, and better understand the origin of ichnofabric-related karst features. Three case studies, which include Pleistocene carbonate rocks of the Biscayne aquifer in southern Florida and Cretaceous carbonate strata of the Edwards–Trinity aquifer system in central Texas, demonstrate that (1) there can be a strong relation between ichnofabrics and groundwater flow in carbonate aquifers and (2) ichnology can offer a useful methodology for carbonate aquifer characterization. In these examples, zones of extremely permeable, ichnofabric-related macroporosity are mappable stratiform geobodies and as such can be represented in groundwater flow and transport simulations.

A Black Hills-Madison Aquifer origin for Dakota Aquifer groundwater in northeastern Nebraska.

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Stotler, Randy; Harvey, F Edwin; Gosselin, David C

2010-01-01

Previous studies of the Dakota Aquifer in South Dakota attributed elevated groundwater sulfate concentrations to Madison Aquifer recharge in the Black Hills with subsequent chemical evolution prior to upward migration into the Dakota Aquifer. This study examines the plausibility of a Madison Aquifer origin for groundwater in northeastern Nebraska. Dakota Aquifer water samples were collected for major ion chemistry and isotopic analysis ((18)O, (2)H, (3)H, (14)C, (13)C, (34)S, (18)O-SO(4), (87)Sr, (37)Cl). Results show that groundwater beneath the eastern, unconfined portion of the study area is distinctly different from groundwater sampled beneath the western, confined portion. In the east, groundwater is calcium-bicarbonate type, with delta(18)O values (-9.6 per thousand to -12.4 per thousand) similar to local, modern precipitation (-7.4 per thousand to -10 per thousand), and tritium values reflecting modern recharge. In the west, groundwater is calcium-sulfate type, having depleted delta(18)O values (-16 per thousand to -18 per thousand) relative to local, modern precipitation, and (14)C ages 32,000 to more than 47,000 years before present. Sulfate, delta(18)O, delta(2)H, delta(34)S, and delta(18)O-SO(4) concentrations are similar to those found in Madison Aquifer groundwater in South Dakota. Thus, it is proposed that Madison Aquifer source water is also present within the Dakota Aquifer beneath northeastern Nebraska. A simple Darcy equation estimate of groundwater velocities and travel times using reported physical parameters from the Madison and Dakota Aquifers suggests such a migration is plausible. However, discrepancies between (14)C and Darcy age estimates indicate that (14)C ages may not accurately reflect aquifer residence time, due to mixtures of varying aged water.

Occurrence of geogenic contaminants in private wells from a crystalline bedrock aquifer in western Quebec, Canada: Geochemical sources and health risks

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Bondu, Raphaël; Cloutier, Vincent; Rosa, Eric

2018-04-01

Nineteen private wells were investigated in order to evaluate the groundwater quality and the issues associated with well water use in a fractured metasedimentary aquifer of the Canadian Shield, in western Quebec (Canada). Groundwater sampling and analysis reveal that the quality of well water is both a potential aesthetic and health concern for the residents. Aesthetic problems are mainly related to the high levels of hardness and dissolved iron and manganese. Potential health risks are associated with the occurrence of brackish groundwater, high manganese concentrations, and arsenic concentrations exceeding the Canadian guideline value of 10 μg/l. Brackish groundwater is suspected to be derived from the mixing of fresh groundwaters with deep calcium-sodium-chloride brines of the Canadian Shield. The occurrences of iron, manganese and arsenic, primarily derived from the natural weathering of bedrock, are highly dependent on the geochemical conditions in groundwater, particularly the redox potential. Arsenic occurs mainly as arsenite (As(III)) and is thought to be released by the dissolution of iron and manganese oxyhydroxides under reducing conditions. Information obtained from well owners indicates that most households use ion exchange water softeners to minimize aesthetic problems of excessive hardness and dissolved iron and manganese concentrations. Homeowners generally take protective measures to reduce their exposure to arsenic when they are aware of the contamination. The exposure to arsenic and manganese may pose health risks for residents that do not take protective measures. The quality of well water is of paramount importance for human health in rural areas. Information on the contaminant sources and individual mitigation measures is essential to assess the health risks associated with groundwater consumption and to ensure the protection of public health.

Characterization of recharge processes in shallow and deeper aquifers using isotopic signatures and geochemical behavior of groundwater in an arsenic-enriched part of the Ganga Plain

International Nuclear Information System (INIS)

Saha, Dipankar; Sinha, U.K.; Dwivedi, S.N.

2011-01-01

Research highlights: → Sub-regional scale aquifers delineated in arsenic-enriched belt in the Ganga Plain. Isotopic fingerprint of the groundwater, from arsenic-enriched and arsenic-safe aquifers established for the first time in the Ganga Plain. → Recharge processes and the water provenances of vertically separated Quaternary aquifers have been established. → Mean residence time of groundwater in the deeper aquifers has been worked out using C-14 isotope. → Water from the deeper aquifer has been correlated with the paleoclimatic model of the Middle Ganga Plain (Mid-Ganga Basin) for 6-2 ka. - Abstract: Arsenic concentrations in groundwater extracted from shallow aquifers in some areas of the Ganga Plain in the states of Bihar and Uttar Pradesh, exceed 50 μg L -1 and locally reach levels in the 400 μg L -1 range. The study covered 535 km 2 of active flood plain of the River Ganga, in Bihar where a two-tier aquifer system has been delineated in a multi-cyclic sequence of Quaternary sand, clay, sandy clay and silty clay all ≤∼250 m below ground surface. The research used isotopic signatures (δ 18 O, δ 2 Η, 3 H, 14 C) and major chemical constituents (HCO 3 - ,SO 4 2- ,NO 3 - ,Cl - ,Ca 2+ ,Mg 2+ ,Na + ,K + ,As total ) of groundwater to understand the recharge processes and groundwater circulation in the aquifers. Values of δ 18 O and δ 2 Η combined with 3 H data indicate that the recharge to the As-enriched top 40 m of the deposits is modern ( -1 ) is hydrologically isolated from the upper aquifer and is characterized by lower 14 C concentration and lower (more negative) δ 18 O values. Groundwater in the lower aquifer is ∼3 ka old, occurs under semi-confined to confined conditions, with hydrostatic head at 1.10 m above the head of the upper aquifer during the pre-monsoon. The recharge areas of the lower aquifer lies in Pleistocene deposits in basin margin areas with the exposed Vindhyan System, at about 55 km south of the area.

GEOCHEMISTRY AND ISOTOPE HYDROLOGY OF AN URBAN AQUIFER, SUBTROPICAL AFRICA, CENTRAL AFRICAN REPUBLIC

International Nuclear Information System (INIS)

HUSSEIN, M.F.; ISLAM, A.; GAMAL, S.; GAETAN, M.; DJEBEBE, C.

2008-01-01

Africa south of the Great Sahara has abundant water resources, however, its aquifers are seldom studied and/or inadequately managed. This study presents a geochemical and isotope hydrology study on the aquifer of Bangui city, the capital of the Central African Republic (RCA), on the northern borders of Congo with RCA.The obtained chemical data demonstrated the role of biogenic CO 2 gas, solid phases and cation exchange in the hydrochemistry of the studied groundwater. The conjunctive use of the major dissolved constituents and the isotope contents ( 18 O and 2 H) showed that the alteration of primary silicates and the dissolution of carbonates are the predominant processes that locally define the zones of dilute and relatively charged groundwater, respectively.The isotope data illustrated that evaporation is non-significantly contributing to the water loss from the aquifer, while transpiration (process that goes almost without isotopic fractionation) is prevailing in the water balance of the local drainage basin, with a significant fraction of the transpired vapour being recycled. An isotopic i nverse continental effect(eastward from Cameron to RCA) is explained through differences in air temperatures, amount and altitude of precipitation rather than by inverse movement of humid air masses westward in Central Africa

Ground-Water Age and Quality in the High Plains Aquifer near Seward, Nebraska, 2003-04

Science.gov (United States)

Stanton, Jennifer S.; Landon, Matthew K.; Turco, Michael J.

2007-01-01

interpret the results, the mean age and mixing fractions from the primary mixing models used were fairly similar. Relations of ground-water age and nitrate concentrations to depth were not consistent across the study area. In some well nests, more young water and nitrate were present near the bottom than in the middle of the aquifer. These results probably reflect pumping from irrigation and supply wells, which are screened primarily in the lower part of the aquifer, and draw younger water downward in the aquifer. Substantial mixing probably occurs because the aquifer is relatively thin (50 feet) and has a relatively high density of wells (about five pumping wells per square mile). The most reliable estimate of horizontal traveltimes based on differences in ground-water ages between a shallow monitoring well at the upgradient end of the northwest well transect and the deep well at the downgradient end of the well transect was 9 years to travel a distance of about 2 miles. The general similarity of ages at similar depths between different well nests is consistent with the fact that horizontal flow in the aquifer is relatively rapid. Concentrations of nitrate (as nitrogen) in untreated ground-water samples from supply wells in the well field were larger than the U.S. Environmental Protection Agency Maximum Contaminant Level for drinking water of 10 mg/L (milligrams per liter), ranging from 11.3 to 13.5 mg/L. It is unlikely that nitrate concentrations in the aquifer near the Seward west well field are decreased by denitrification in the aquifer due to oxic geochemical conditions that preclude this reaction. Nitrate concentrations coupled with water recharge dates were compared to historical estimated fertilizer application in an attempt to reconstruct historical trends in ground-water nitrate concentrations and their relation to land-use practices. Nitrate concentrations in young-water fractions, after adjustment for mixing, may be decreasing over apparent recharg

Geochemical Characteristics of Shallow Groundwater in Jiaoshiba Shale Gas Production Area: Implications for Environmental Concerns

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Yiman Li

2016-11-01

Full Text Available The geochemical characteristics of shallow groundwater are essential for environmental impact studies in the shale gas production area. Jiaoshiba in the Sichuan basin is the first commercial-scale shale gas production area in China. This paper studied the geochemical and isotopic characteristics of the shallow groundwater of the area for future environmental concerns. Results show that the average pH of the shallow groundwater is 7.5 and the total dissolved solids (TDS vary from 150 mg/L to 350 mg/L. The main water types are HCO3-Ca and HCO3-Ca·Mg due to the carbonates dissolution equilibrium in karst aquifers. The concentrations of major ions and typical toxic elements including Mn, Cr, Cu, Zn, Ba, and Pb are below the drinking water standard of China and are safe for use as drinking water. The high nitrate content is inferred to be caused by agricultural pollution. The shallow groundwater is recharged by local precipitation and flows in the vertical circulation zone. Evidences from low TDS, water isotopes, and high 3H and 14C indicate that the circulation rate of shallow groundwater is rapid, and the lateral groundwater has strong renewability. Once groundwater pollution from deep shale gas production occurs, it will be recovered soon by enough precipitation.

Evaluation of conceptual and numerical models for arsenic mobilization and attenuation during managed aquifer recharge.

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Wallis, Ilka; Prommer, Henning; Simmons, Craig T; Post, Vincent; Stuyfzand, Pieter J

2010-07-01

Managed Aquifer Recharge (MAR) is promoted as an attractive technique to meet growing water demands. An impediment to MAR applications, where oxygenated water is recharged into anoxic aquifers, is the potential mobilization of trace metals (e.g., arsenic). While conceptual models for arsenic transport under such circumstances exist, they are generally not rigorously evaluated through numerical modeling, especially at field-scale. In this work, geochemical data from an injection experiment in The Netherlands, where the introduction of oxygenated water into an anoxic aquifer mobilized arsenic, was used to develop and evaluate conceptual and numerical models of arsenic release and attenuation under field-scale conditions. Initially, a groundwater flow and nonreactive transport model was developed. Subsequent reactive transport simulations focused on the description of the temporal and spatial evolution of the redox zonation. The calibrated model was then used to study and quantify the transport of arsenic. In the model that best reproduced field observations, the fate of arsenic was simulated by (i) release via codissolution of arsenopyrite, stoichiometrically linked to pyrite oxidation, (ii) kinetically controlled oxidation of dissolved As(III) to As(V), and (iii) As adsorption via surface complexation on neo-precipitated iron oxides.

Occurrence and geochemical behavior of arsenic in a coastal aquifer–aquitard system of the Pearl River Delta, China

International Nuclear Information System (INIS)

Wang, Ya; Jiao, Jiu Jimmy; Cherry, John A.

2012-01-01

Elevated concentrations of arsenic, up to 161 μg/L, have been identified in groundwater samples from the confined basal aquifer underlying the aquitard of the Pearl River Delta (PRD). Both aquatic arsenic in pore water and solid arsenic in the sediments in the basal aquifer and aquitard were identified. Arsenic speciation of groundwater in the basal aquifer was elucidated on a pH-Eh diagram. In the PRD, arsenic is enriched in groundwater having both low and high salinity, and arsenic enriched groundwater is devoid of dissolved oxygen, has negative Eh values, is slightly alkaline, and has abnormally high concentrations of ammonium and dissolved organic carbon, but low concentrations of nitrate and nitrite. Results of geochemical and hydrochemical analyses and sequential extraction analysis suggest that reductive dissolution of iron oxyhydroxide could be one of the important processes that mobilized solid arsenic. We speculate that mineralization of sedimentary organic matter could also contribute to aquatic arsenic. Scanning electron microscope analysis confirms that abundant authigenic pyrite is present in the sediments. Sulphate derived from paleo-seawater served as the important sulfur source for authigenic pyrite formation. Co-precipitation of arsenic with authigenic pyrite significantly controlled concentrations of aquatic arsenic in the coastal aquifer–aquitard system. - Highlights: ► Coastal aquifer and aquitard are treated as an integrate system. ► Both aquatic arsenic and solid arsenic are observed. ► Aquatic arsenic is derived from reductive dissolution of iron oxyhydroxide. ► Aquatic arsenic can also derived from mineralization of sedimentary organic matter. ► Co-precipitation of arsenic with authigenic pyrite is significant in such a system.

Aquifers of Arkansas: protection, management, and hydrologic and geochemical characteristics of groundwater resources in Arkansas

Science.gov (United States)

Kresse, Timothy M.; Hays, Phillip D.; Merriman, Katherine R.; Gillip, Jonathan A.; Fugitt, D. Todd; Spellman, Jane L.; Nottmeier, Anna M.; Westerman, Drew A.; Blackstock, Joshua M.; Battreal, James L.

2014-01-01

Sixteen aquifers in Arkansas that currently serve or have served as sources of water supply are described with respect to existing groundwater protection and management programs, geology, hydrologic characteristics, water use, water levels, deductive analysis, projections of hydrologic conditions, and water quality. State and Federal protection and management programs are described according to regulatory oversight, management strategies, and ambient groundwater-monitoring programs that currently (2013) are in place for assessing and protecting groundwater resources throughout the State.

New methodology for aquifer influx status classification for single wells in a gas reservoir with aquifer support

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Yong Li

2016-10-01

Full Text Available For gas reservoirs with strong bottom or edge aquifer support, the most important thing is avoiding aquifer breakthrough in a gas well. Water production in gas wells does not only result in processing problems in surface facilities, but it also explicitly reduces well productivity and reservoir recovery. There are a lot of studies on the prediction of water breakthrough time, but they are not completely practicable due to reservoir heterogeneity. This paper provides a new method together with three diagnostic curves to identify aquifer influx status for single gas wells; the aforementioned curves are based on well production and pressure data. The whole production period of a gas well can be classified into three periods based on the diagnostic curves: no aquifer influx period, early aquifer influx period, and middle-late aquifer influx period. This new method has been used for actual gas well analysis to accurately identify gas well aquifer influx status and the water breakthrough sequence of all wells in the same gas field. Additionally, the evaluation results are significantly beneficial for well production rate optimization and development of an effective gas field.

Geochemical model of uranium and selenium in an aquifer disturbed by in situ uranium mining

International Nuclear Information System (INIS)

Johnson, K.; Neumann, M.R.

1986-01-01

Restoring ground water to baseline conditions proved to be very difficult, however, and led to the trial of a sodium carbonate/bicarbonate lixiviant. Results of this test indicated the basic lixiviant was unable to address uranium tied up in carbonaceous material. Subsequently, the decision was made to curtail development and restore all affected ground water to the extent achievable through the use of the best practicable technology, such as reverse osmosis. Restoration results, however, were not considered adequate for demonstration of commercial restoration feasibility. Following completion of the restoration effort, regulatory agencies expressed concern as to the long-term fate of certain parameters, such as uranium and selenium, remaining in solution at above baseline levels. Rocky Mountain Energy, through discussions with various consultants, determined that geochemical modeling would be the most appropriate tool for predicting the probable long-term effects. This paper summarizes the results of the subsequent evaluation which was conducted using the PHREEQE computer model. Significant conclusions of the investigation were: (1) the Eh in the ground water decreases regularly after mining activities, as shown by measured Eh values, and (2) the accompanying decrease in uranium and selenium can be predicted by thermodynamic modeling

Microbial and geochemical investigations of dissolved organic carbon and microbial ecology of native waters from the Biscayne and Upper Floridan Aquifers

Science.gov (United States)

Lisle, John T.; Harvey, Ron W.; Aiken, George R.; Metge, David W.

2010-01-01

Groundwater resources in the United States are under ever-increasing demands for potable, irrigation, and recreational uses. Additionally, aquifer systems are being used or targeted for use as storage areas for treated surface waters and (or) groundwaters via injection (for example, aquifer storage and recovery). To date, the influence that the nutrients, including carbon, in the injected water have on native microbial communities and the biogeochemistry in the subsurface zones used for storage of the injectate has not been determined. In this report, we describe a series of experiments that establishes a baseline dataset for the quantity and quality of organic and inorganic carbon and nutrients in the Biscayne Aquifer (BA) and Upper Floridan Aquifer (UFA) in south Florida. The most significant differences between the BA (26 meters below surface) and UFA (366 meters below surface) are the average specific conductance (0.552 and 6.12 microsiemens per centimeter, respectively), dissolved oxygen (1.6 and 0 milligrams per liter, respectively), and oxidation-reduction potential (40.3 and -358 millivolts, respectively). The dissolved organic carbon from the BA is characterized by carbon originating from terrestrial sources and microbial activities, while the UFA has a distinctive microbial signature. Acetate and lactate are the dominant carbon constituents in both aquifers. Additionally, components of the dissolved organic carbon from the UFA have a total trihalomethane-formation potential that is approximately threefold greater than the maximum contaminat level of 80 micrograms per liter established by the U.S. Environmental Protection Agency. The average native bacterial abundances in the aquifers are similar with 4.69x10^4 cells per milliliter in the BA and 1.33x10^4 cells per milliliter in the UFA. The average bacteriophage abundances are also similar with 1.15x10^5 virus-like particles in the BA and 1.92x10^5 virus-like particles in the UFA. Interestingly, ciliated

Preliminary reactive geochemical transport simulation study on CO2 geological sequestration at the Changhua Coastal Industrial Park Site, Taiwan

Science.gov (United States)

Sung, R.; Li, M.

2013-12-01

assumed throughout the simulation domain. Comparisons among simulated results with different mesh systems of nested meshes and non-nested meshes and considerations of multiphase reactive transport and physical transport were demonstrated in this study. Preliminary results of injection CO2 for 50 years are: (1) about 7 wt.% of injected CO2 was trapped as carbonate minerals mainly as ankerite; (2) porosities were decreased by 0.014 % and increased by 0.102 % at the injection point and beneath the cap rock, respectively, and were subsequently decreased with time due to minerals precipitation mostly as illite and ankerite; (3) differences of simulated aquifer responses between reactive transport and physical transport were insignificant; and (4) projected CO2 plumes with the nested meshes was smaller than those by the non-nested meshes after cease of CO2 injection. Keywords: CO2-Saline-Mineral Interaction, Reactive Geochemical Transport, TOUGHREACT, Mineral Trapping Assessment, Changhua Costal Industrial Park Site, Taiwan Reference: Marini, L., 2006, Geological Sequestration of Carbon Dioxide, Volume 11: Thermodynamics, Kinetics, and Reaction Path Modeling, Elsevier Science, pp.470. Xu, T., J. A. Apps and K. Pruess, 2004, Numerical simulation of CO2 disposal by mineral trapping in deep aquifers, Applied Geochemistry, Vol. 19:917-936.

Uruguay mining Inventory: geochemical prospecting results of Cerro de las Cuentas mapping

International Nuclear Information System (INIS)

Spangenberg, J.; Filippini, J.

1986-01-01

This work is about the geochemical prospecting carried out into the Uruguay mining inventory framework. In this case the survey was in Cerro de las Cuentas mapping. Cerro Largo department. Scale 1 / 50000.

Hydrogeology and water quality of the Floridan aquifer system and effect of Lower Floridan aquifer withdrawals on the Upper Floridan aquifer at Barbour Pointe Community, Chatham County, Georgia, 2013

Science.gov (United States)

Gonthier, Gerard; Clarke, John S.

2016-06-02

Two test wells were completed at the Barbour Pointe community in western Chatham County, near Savannah, Georgia, in 2013 to investigate the potential of using the Lower Floridan aquifer as a source of municipal water supply. One well was completed in the Lower Floridan aquifer at a depth of 1,080 feet (ft) below land surface; the other well was completed in the Upper Floridan aquifer at a depth of 440 ft below land surface. At the Barbour Pointe test site, the U.S. Geological Survey completed electromagnetic (EM) flowmeter surveys, collected and analyzed water samples from discrete depths, and completed a 72-hour aquifer test of the Floridan aquifer system withdrawing from the Lower Floridan aquifer.Based on drill cuttings, geophysical logs, and borehole EM flowmeter surveys collected at the Barbour Pointe test site, the Upper Floridan aquifer extends 369 to 567 ft below land surface, the middle semiconfining unit, separating the two aquifers, extends 567 to 714 ft below land surface, and the Lower Floridan aquifer extends 714 to 1,056 ft below land surface.A borehole EM flowmeter survey indicates that the Upper Floridan and Lower Floridan aquifers each contain four water-bearing zones. The EM flowmeter logs of the test hole open to the entire Floridan aquifer system indicated that the Upper Floridan aquifer contributed 91 percent of the total flow rate of 1,000 gallons per minute; the Lower Floridan aquifer contributed about 8 percent. Based on the transmissivity of the middle semiconfining unit and the Floridan aquifer system, the middle semiconfining unit probably contributed on the order of 1 percent of the total flow.Hydraulic properties of the Upper Floridan and Lower Floridan aquifers were estimated based on results of the EM flowmeter survey and a 72-hour aquifer test completed in Lower Floridan aquifer well 36Q398. The EM flowmeter data were analyzed using an AnalyzeHOLE-generated model to simulate upward borehole flow and determine the transmissivity of

Hydrochemical Regions of the Glacial Aquifer System, Northern United States, and Their Environmental and Water-Quality Characteristics

Science.gov (United States)

Arnold, Terri L.; Warner, Kelly L.; Groschen, George E.; Caldwell, James P.; Kalkhoff, Stephen J.

2008-01-01

The glacial aquifer system in the United States is a large (953,000 square miles) regional aquifer system of heterogeneous composition. As described in this report, the glacial aquifer system includes all unconsolidated geologic material above bedrock that lies on or north of the line of maximum glacial advance within the United States. Examining ground-water quality on a regional scale indicates that variations in the concentrations of major and minor ions and some trace elements most likely are the result of natural variations in the geologic and physical environment. Study of the glacial aquifer system was designed around a regional framework based on the assumption that two primary characteristics of the aquifer system can affect water quality: intrinsic susceptibility (hydraulic properties) and vulnerability (geochemical properties). The hydrochemical regions described in this report were developed to identify and explain regional spatial variations in ground-water quality in the glacial aquifer system within the hypothetical framework context. Data analyzed for this study were collected from 1991 to 2003 at 1,716 wells open to the glacial aquifer system. Cluster analysis was used to group wells with similar ground-water concentrations of calcium, chloride, fluoride, magnesium, potassium, sodium, sulfate, and bicarbonate into five unique groups. Maximum Likelihood Classification was used to make the extrapolation from clustered groups of wells, defined by points, to areas of similar water quality (hydrochemical regions) defined in a geospatial model. Spatial data that represented average annual precipitation, average annual temperature, land use, land-surface slope, vertical soil permeability, average soil clay content, texture of surficial deposits, type of surficial deposit, and potential for ground-water recharge were used in the Maximum Likelihood Classification to classify the areas so the characteristics of the hydrochemical regions would resemble the

Rare earth elements and uranium in groundwater under influence of distinct aquifers in Campinas, SP, Brazil; Elementos terras raras e uranio em aguas subterraneas sob influencia de aquiferos distintos em Campinas (SP)

Energy Technology Data Exchange (ETDEWEB)

Bulia, Isabella Longhi; Enzweiler, Jacinta, E-mail: isabellalonghi@ige.unicamp.br, E-mail: jacinta@ige.unicamp.br [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Instituto de Geociencias

2015-07-01

The composition of groundwaters results mainly from water-rock reactions within aquifers. Among the various constituents of water, the rare earth elements (REE) and uranium can serve as tracers of geochemical processes and hydrological flow paths. The main objective of this study was to associate the chemical composition of groundwaters extracted from three distinct aquifer systems (crystalline, diabase and sedimentary) with that of the respective hosts rocks. The area of the study is located at the campus of University of Campinas (Campinas, SP). Samples of groundwater collected from four tubular wells were used to determine physicochemical parameters, major ions and trace elements, including the REE. The results confirm that the water of two wells (IMECC and IB) is predominantly influenced by the crystalline and diabase aquifers, while the other two (GM and FEF) by the sedimentary aquifer. Both the individual and normalized REE values of the four wells are distinct from each other, pointing to the heterogeneity of the local geology. The uranium concentration in the water of one well (GM) exceeded the guideline value for this element in drinking water. The U probably results from the oxidative dissolution of U-bearing phases in the sedimentary aquifer. However, the hydrochemical modeling indicated Ca{sub 2}UO{sub 2}(CO{sub 3}){sub 3} and CaUO{sub 2}(CO{sub 3}){sub 2}{sup 2-} as the major U dissolved species, which are considered non-toxic and non-bioavailable according to literature data. (author)

Identifying functional zones of denitrification in heterogeneous aquifer systems by numerical simulations - a case study

Science.gov (United States)

Jang, E.; Kalbacher, T.; He, W.; Shao, H.; Schueth, C.; Kolditz, O.

2014-12-01

Nitrate contamination in shallow groundwater is still one of the common problems in many countries. Because of its high solubility and anionic nature, nitrate can easily leach through soil and persist in groundwater for decades. High nitrate concentration has been suggested as a major cause of accelerated eutrophication, methemoglobinemia and gastric cancer. There are several factors influencing the fate of nitrate in groundwater system, which is e.g. distribution of N- sources to soil and groundwater, distribution and amount of reactive substances maintaining denitrification, rate of nitrate degradation and its kinetics, and geological characteristics of the aquifer. Nitrate transport and redox transformation processes are closely linked to complex and spatially distributed physical and chemical interaction, therefore it is difficult to predict and quantify in the field and laboratory experiment. Models can play a key role in elucidation of nitrate reduction pathway in groundwater system and in the design and evaluation of field tests to investigate in situ remediation technologies as well. The goal of the current study is to predict groundwater vulnerability to nitrate, to identify functional zones of denitrification in heterogeneous aquifer systems and to describe the uncertainty of the predictions due to scale effects. For this aim, we developed a kinetic model using multi-component mass transport code OpenGeoSys coupling with IPhreeqc module of the geochemical solver PHREEQC. The developed model included sequential aerobic and nitrate-based respiration, multi-Monod kinetics, multi-species biogeochemical reactions, and geological characteristics of the groundwater aquifer. Moreover water-rock interaction such as secondary mineral precipitation was also included in this model. In this presentation, we focused on the general modelling approach and present the simulation results of nitrate transport simulation in a hypothetical aquifer systems based on data from

Corrigenda: Epigean and hypogean Palaemonetes sp. (Decapoda, Palaemonidae from Edwards Aquifer: An examination of trophic structure and metabolism. Subterranean Biology 14: 79–102.

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Renee Bishop

2015-06-01

Full Text Available This study addresses the causes of the metabolic depression observed when examining the metabolism of hypogean versus epigean organisms. We examined the two current hypotheses regarding the cause of metabolic cave adaptation, a paucity of food and low oxygen availability, both necessary for ATP production, by first determining if the hypogean environment examined, Edwards Aquifer, was resource limited. Stable isotope analyses indicate that there is extensive microbial chemolithoautotrophic production providing resources for the hypogean organisms. δ13C values ( ≤30‰ were well below that of terrestrial biome indicating that C in the aquifer originates from chemolithoautotrophic inorganic carbon fixation, not photosynthetically derived material resulting from terrigenous sources. Data suggest the artesian system is a complex geochemical ecosystem providing inorganic energy sources from both methane and sulfates. Metabolism, examined via key aerobic and anaerobic proxies, and organismal proximate composition indicated there was no difference between metabolic rates and energy storage of Palaemonetes antrorum (stygobitic and Palaemonetes kadiakensis (epigean. This indicates that resources within the oxic aquifer are not limited. We demonstrate that it is necessary for one, or both, of these selective pressures to be present for metabolic cave adaptation to occur.

Joint Russian-American hydrogeological-geochemical studies of the Karachai-Mishelyak system, South Urals, Russia

International Nuclear Information System (INIS)

Drozhko, E.G.; Glagolenko, Y.U.; Mokrov, Y.G.; Postovalova, G.A.; Samsonova, L.M.; Glagolev, A.V.; Ter-Saakian, S.A.; Glinsky, M.L.; Vasil'kova, N.A.; Skokov, A.V.; Wollenberg, H.A.; Tsan, C.F.; Frangos, W.; Solbau, R.D.; Stevenson, K.A.

1997-01-01

In September 1994, a Russian-American team conducted hydrogeological, geochemical, geophysical, and radiometric measurements in the teritory of the Mayak Production Association, Russia. The primary purpose of these operations was to examine the frontal area of a radioelement- and nitrate-laden groundwater plume moving from the disposal site, Lake Karachai, toward the Mishelyak River. Activities encompassed (1) isolation of hydrologic intervgals in two wells and production of water from these intervals, to comapre isolated versus open-well sampling methods and to determine hydraulic transmissivities of the aquifer(s); (2) surface and soil-water sampling, accompanying radiometric measurements and subsequent chemical analyses; and (3) electrical resistivity profiling in areas of expected contrasting resistivity. Preliminary results indicate that (1) 60 Co, 137 Cs, and 90 Sr are present in small concentrations (∝0.1% of permissible levels) in water of the Mishelyak River; (2) analyses of water samples collected by a downhole sampler and of water produced from packed-off intevals agree within limits of laboratory accuracy, attesting to the efficacy of the sampling methods presently used by the Russian workers; (3) considerable differences in contaminant concentrations exist between nearby wells, supporting the concept that the plume from Lake Karachai toward the Mishelyak River is controlled by steeply dipping fractures and shear zones; and (4) strong contrasts occur between the electrical resistivities of soil and bedrock. (orig./SR)

Appliance of geochemical engineering in radioactive waste disposal

International Nuclear Information System (INIS)

Li Shuang; Zhang Chengjiang; Ni Shijun; Li Kuanliang

2008-01-01

The basic foundation of applying geochemical engineering to control environment, common engineering models of disposal radioactive waste and the functions of the engineering barriers are introduced in this paper. The authors take the geochemical engineering barrier materiel research of a radioactive waste repository as an example to explain the appliance of geochemical engineering in the disposal of radioactive waste. And the results show that it can enhance the security of the nuclear waste repository if we use geochemical engineering barrier. (authors)

The usefulness of multi-well aquifer tests in heterogeneous aquifers

International Nuclear Information System (INIS)

Young, S.C.; Benton, D.J.; Herweijer, J.C.; Sims, P.

1990-01-01

Three large-scale (100 m) and seven small-scale (3-7 m) multi-well aquifer tests were conducted in a heterogeneous aquifer to determine the transmissivity distribution across a one-hectare test site. Two of the large-scale tests had constant but different rates of discharge; the remaining large-scale test had a discharge that was pulsed at regulated intervals. The small-scale tests were conducted at two well clusters 20 m apart. The program WELTEST was written to analyze the data. By using the methods of non-linear least squares regression analysis and Broyden's method to solve for non-linear extrema, WELTEST automatically determines the best values of transmissivity and the storage coefficient. The test results show that order of magnitude differences in the calculated transmissivities at a well location can be realized by varying the discharge rate at the pumping well, the duration of the aquifer test, and/or the location of the pumping well. The calculated storage coefficients for the tests cover a five-order magnitude range. The data show a definite trend for the storage coefficient to increase with the distance between the pumping and the observation wells. This trend is shown to be related to the orientation of high hydraulic conductivity zones between the pumping and the observation wells. A comparison among single-well aquifer tests, geological investigations and multi-well aquifer tests indicate that the multi-well tests are poorly suited for characterizing a transmissivity field. (Author) (11 refs., 14 figs.)

Using enteric pathogens to assess sources of fecal contamination in the Silurian Dolomite Aquifer: Preliminary results

Science.gov (United States)

Muldoon, Maureen A; Borchardt, Mark A.; Spencer, Susan K.; Hunt, Randall J.; Owens, David

2018-01-01

The fractured Silurian dolomite aquifer is an important, but vulnerable, source of drinking water in northeast Wisconsin (Sherrill in Geology and ground water in Door County, Wisconsin, with emphasis on contamination potential in the Silurian dolomite, 1978; Bradbury and Muldoon in Hydrogeology and groundwater monitoring of fractured dolomite in the Upper Door Priority Watershed, Door County, Wisconsin, 1992; Muldoon and Bradbury in Assessing seasonal variations in recharge and water quality in the Silurian aquifer in areas with thicker soil cover. p 45, 2010). Areas underlain by the Silurian dolomite aquifer are extremely vulnerable to groundwater contamination from various land-use activities, especially the disposal of human wastewater and dairy manure. Currently there is no consensus as to which source of wastewater generates the greater impact to the aquifer.

Hydrogeology and results of aquifer tests in the vicinity of a hazardous-waste disposal site near Byron, Illinois

Science.gov (United States)

Kay, Robert T.; Olson, David N.; Ryan, Barbara J.

1989-01-01

The U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, conducted an investigation of a Superfund Site near Byron, Illinois. The purpose of the investigation was to determine the hydrogeologic properties of the Galena-Platteville and St. Peter aquifers, the primary water-supply aquifers for domestic supply in the area. The Galena and Platteville Groups and older St. Peter Sandstone are separated by the Harmony Hill Shale Member of the Glenwood Formation. The Harmony Hill Shale Member is a semiconfining unit. Groundwater flow in the study area is from the site northwestward to the Rock River. Movement of groundwater in the dolomites is mainly through joints, fractures, and solution openings. Analysis of the Galena-Platteville aquifer-test data indicates that the calculated aquifer transmissivity ranges from 490 to 670 sq ft/day, and the calculated specific yield ranges from 0.017 to 0.140. Aquifer test data also indicate that the Galena-Platteville aquifer is heterogeneous and anisotropic. Analysis of the St. Peter aquifer-test data indicates that the calculated transmissivity of the aquifer ranges from 1,200 to 1 ,305 sq ft/day, storativity ranges from 0.000528 to 0.00128, horizontal hydraulic conductivity ranges from 2.9 to 3.1 ft/day, and leakage through the Harmony Hill Shale Member ranges from .000123 to .000217 ft/day/ft. (USGS)

Ground-water quality assessment of the central Oklahoma Aquifer, Oklahoma; project description

Science.gov (United States)

Christenson, S.C.; Parkhurst, D.L.

1987-01-01

, selenium, and gross-alpha activity that exceed drinking-water standards. Suspected problems include possible contamination of the aquifer by oil-field brines and drilling fluids, pesticides, industrial chemicals, septic-tank effluent, fertilizers, and leakage from sewage systems and underground tanks used for storage of hydrocarbons. There are four major components of the Central Oklahoma aquifer project. The first component is the collection and analysis of existing information, including chemical, hydrologic, and land-use data. The second component is the geohydrologic and geochemical investigations of the aquifer flow system. The third component is the sampling for a wide variety of inorganic, organic, and radioactive constituents as part a regional survey that will produce a consistent set of data among all ground-water pilot projects. These data can be used to: (1) Define regional ground-water quality within the Central Oklahoma aquifer, and (2) compare water quality in the Central Oklahoma aquifer to the water quality in the other ground-water study units of the NAWQA program. The fourth component is topical studies that will address, in more detail, some of the major water-quality issues pertaining to the aquifer.

Recharge and Aquifer Response: Manukan Island’s Aquifer, Sabah, Malaysia

Directory of Open Access Journals (Sweden)

Sarva Mangala Praveena

2010-01-01

Full Text Available Manukan Island is a small island located in North-West of Sabah, Malaysia was used as a case study area for numerical modeling of an aquifer response to recharge and pumping rates. The results in this study present the variations of recharge into the aquifer under the prediction simulations. The recharge rate increases the water level as indicated by hydraulic heads. This shows that it can alter groundwater of Manukan Island which has been suffering from an overexploration in its unconfined the aquifer. The increase in recharge rate (from 600 mm/year to 750 mm/year increases the water level indicated by hydraulic heads. A reduction in pumping rate (from 0.072 m3/day to 0.058 m3/day not only increases the amount of water levels in aquifer but also reduces the supply hence a deficit in supply. The increase in hydraulic heads depends on the percentage reduction of pumping and recharges rates. The well water has 1978.3 mg/L chloride with current pumping (0.072 m3/day and recharge rates (600 mm/year. However, with an increased of recharge rate and current pumping rate it has decreased about 1.13%. In addition, reduction in pumping rate made the chloride concentration decreased about 2.8%. In general, a reduction in pumping with an increase in recharge rate leads to a decreased in chloride concentrations within the vicinity of cone of depression. Next, to further develop the numerical model, the model should focus on climate change variables such as consequences of climate change are increase in air temperature, increase in sea surface temperature, and more extreme weather conditions. These parameters are considered critical parameters for climate change impact modeling in aquifers. The behavior of the aquifer and its sustainable pumping rate can be done by applying a computer modeling component.

Assessing the vulnerability of public-supply wells to contamination—Edwards aquifer near San Antonio, Texas

Science.gov (United States)

Jagucki, Martha L.; Musgrove, MaryLynn; Lindgren, Richard J.; Fahlquist, Lynne; Eberts, Sandra M.

2011-01-01

This fact sheet highlights findings from the vulnerability study of a public-supply well field in San Antonio, Texas. The well field consists of six production wells that tap the Edwards aquifer. Typically, one or two wells are pumped at a time, yielding an average total of 20-21 million gallons per day. Water samples were collected from public-supply wells in the well field and from monitoring wells installed along general directions of flow to the well field. Samples from the well field contained some constituents of concern for drinking-water quality, including nitrate; the pesticide compounds atrazine, deethylatrazine, and simazine; and the volatile organic compounds tetrachloroethene (also called perchloroethene, or PCE), chloroform, bromoform, and dibromochloromethane. These constituents were detected in untreated water at concentrations much less than established drinking-water standards, where such standards exist. Overall, the study findings point to four primary factors that affect the movement and fate of contaminants and the vulnerability of the public-supply well field in San Antonio, Texas: (1) groundwater age (how long ago water entered, or recharged, the aquifer), (2) fast pathways for flow of groundwater through features formed or enlarged by dissolution of bedrock, (3) recharge characteristics of the aquifer, and (4) natural geochemical processes within the aquifer. A computer-model simulation of groundwater flow and transport was used to estimate the traveltime (or age) of water particles entering public-supply well W4 in the well field. Modeled findings show that almost half of the water reaching the public-supply well is less than 2 years old. Such a large percentage of very young water indicates that (1) contaminants entering the aquifer may be transported rapidly to the well, (2) there is limited time for chemical reactions to occur in the aquifer that may attenuate contaminants, and (3) should recharge water become contaminated with

Apports des analyses chimiques et isotopiques à la connaissance du fonctionnement des aquifères plio-quaternaire et turonien de la zone synclinale d'Essaouira, Maroc occidentalGeochemistry of Plio-Quaternary and Turonian aquifers in the Essaouira Basin, western Moroco

Science.gov (United States)

Mennani, A.; Blavoux, B.; Bahir, M.; Bellion, Y.; Jalal, M.; Daniel, M.

2001-05-01

The Essaouira synclinal zone is one of the Moroccan semi-arid zones with annual rainfalls not exceeding 300 mm yr -1 and very high potential evapo-transpiration of about 920 mm yr -1. This syncline with a Senonian axial zone is bordered by two diapiric structures of Triassic deposits: the Tidzi Diapir that outcrops in the east and south, and the hidden Essaouira diapir in the west, which was found by geophysics. This syncline contains two main superimposed aquifers. (i) The Plio-Quaternary aquifer consists of sands, sandstone and conglomerates and provides the main part of the water supply. This free-water table flows out towards the northwest and its surface is affected by significant piezometric variations. (ii) The calcareous dolomitic Turonian is a confined aquifer under the Senonian marls in the and in direct contact with the Plio-Quaternary. For a few years, the drinking water supply to the town of Essaouira has come from deep drillings. These two aquifers were sampled in June 1995 and in Januray 1996 after exceptional rainfalls. All waters have the same geochemical profile. The interpretation of the total dissolved solids and chloride content of Plio-Quaternary aquifers makes it possible to specify their origins. It emphasises, in particular, the source from the Ksob Wadi in the northeast and the role of the hidden Essaouira diapir. Nitrate levels were raised excessively, increasing at the same time as chloride concentrations during the rains of the winter of 1996, and underline the wells vulnerability to pastoral and domestic activities. The interpretation of O- and H-isotopes distinguishes two contrasting Plio-Quaternary and Turonian aquifers with an Atlantic origin for the rain recharge. A specific campaign was varried out in November 1996 to date water from the Turonian aquifer by 14C. Two boreholes draw water of several thousands years old.

Natural Tracers and Isotope Techniques to Define Groundwater Recharge and Salinization in the Bou Areg Coastal Aquifer (North Morocco)

Energy Technology Data Exchange (ETDEWEB)

Re, V. [Department of Molecular Sciences and Nanosystems, University Ca' Foscari, Venice (Italy); Allais, E. [ISO4 s.n.c., Torino (Italy); El Hamouti, N. [Multidisciplinary Faculty of Nador, University of Oujda, Nador (Morocco); Bouchnan, R. [Laboratory of Physical Phenomena and Natural Risk Modelling, University of Tangier, Tangier (Morocco); Sacchi, E. [Department of Earth Sciences, University of Pavia, Pavia (Italy); Rizzo, F. [UNESCO International Hydrological Programme, Paris (France); Zuppi, G. M. [Department of Molecular Sciences and Nanosystems, University Ca' Foscari, Venice and Institute of Environmental Geology and Geoengineering, National Research Council, Monterotondo (Italy)

2013-07-15

The geochemical and isotopic ({delta}{sup 2}H, {delta}{sup 18}O, {delta}{sup 13}C, {delta}{sup 15}N{sub NO3},{delta} {sup 18}O{sub NO3}) characterization of the Bou Areg aquifer (North Morocco) based on samples collected during two surveys in November 2009 and June 2010 allowed the identification of run-off from the mountain regions and agricultural return flows as the main sources of aquifer recharge. The high salinization of the aquifer is not only due to the intensive agricultural activities but it is also associated with the natural quality of the catchment. The isotopic signal of dissolved nitrates allowed for the identification of two main sources of nitrogen in the system: (i) fertilizers and (ii) manure and septic effluents. The study, framed within the UNESCO-IHP sub component of the Strategic Partnership for the Mediterranean Large Marine Ecosystem, represents the first isotopic investigation of the area and will serve as a basis for the promotion of robust science based management practices in the region. (author)

A Combined Radio- and Stable-Isotopic Study of a California Coastal Aquifer System

Directory of Open Access Journals (Sweden)

Michael Land

2013-04-01

Full Text Available Stable and radioactive tracers were utilized in concert to characterize geochemical processes in a complex coastal groundwater system and to provide constraints on the kinetics of rock/water interactions. Groundwater samples from wells within the Dominguez Gap region of Los Angeles County, California were analyzed for a suite of major cations (Na+, K+, Mg2+, Ca2+ and anions (Cl−, SO42−, silica, alkalinity, select trace elements (Ba, B, Sr, dissolved oxygen, stable isotopes of hydrogen (δD, oxygen (δ18O, dissolved inorganic carbon (δ13CDIC, and radioactive isotopes (3H, 222Rn and 223,224,226,228Ra. In the study area, groundwater may consist of a complex mixture of native groundwater, intruded seawater, non-native injected water, and oil-field brine water. In some wells, Cl− concentrations attained seawater-like values and in conjunction with isotopically heavier δ18O values, these tracers provide information on the extent of seawater intrusion and/or mixing with oil-field brines. Groundwater 3H above 1 tritium unit (TU was observed only in a few select wells close to the Dominguez Gap area and most other well groundwater was aged pre-1952. Based on an initial 14C value for the study site of 90 percent modern carbon (pmc, groundwater age estimates likely extend beyond 20 kyr before present and confirm deep circulation of some native groundwater through multiple aquifers. Enriched values of groundwater δ13CDIC in the absence of SO42− imply enhanced anaerobic microbial methanogenesis. While secular equilibrium was observed for 234U/238U (activity ratios ~1 in host matrices, strong isotopic fractionation in these groundwater samples can be used to obtain information of adsorption/desorption kinetics. Calculated Ra residence times are short, and the associated desorption rate constant is about three orders of magnitude slower than that of the adsorption rate constant. Combined stable- and radio-isotopic results provide unique insights

Hydrogeochemical Impact of CO₂ Leakage from Geological Sequestration on Shallow Potable Aquifers

DEFF Research Database (Denmark)

Cahill, Aaron Graham

. Although considered highly unlikely following appropriate site selection, leakage of CO2 from CCGS forms a major concern for both scientists and the public. Leakage would potentially occur through faults or abandoned boreholes and ultimately result in upward migration and discharge to the atmosphere....... During migration CO2 would dissolve into groundwater forming carbonic acid, induce water-rock reactions and thus change groundwater chemistry. Therefore prior to implementation of this potentially necessary technology, environmental risks associated with leakage must be understood. Over the past 10 years...... it be detected geochemically? Some common hydrochemical development is apparent from the literature however many aspects of hydrogeological and hydrogeochemical impact of leakage into shallow aquifers used in water supply remain unclear. In this Ph.D. study an integrated approach was employed in order to answer...

Mercury concentration, speciation and budget in volcanic aquifers: Italy and Guadeloupe (Lesser Antilles)

Science.gov (United States)

Bagnato, E.; Aiuppa, A.; Parello, F.; D'Alessandro, W.; Allard, P.; Calabrese, S.

2009-01-01

Quantifying the contribution of volcanism to global mercury (Hg) emissions is important to understand the pathways and the mechanisms of Hg cycling through the Earth's geochemical reservoirs and to assess its environmental impacts. While previous studies have suggested that degassing volcanoes might contribute importantly to the atmospheric budget of mercury, little is known about the amount and behaviour of Hg in volcanic aquifers. Here we report on detailed investigations of both the content and the speciation of mercury in aquifers of active volcanoes in Italy and Guadeloupe Island (Lesser Antilles). In the studied groundwaters, total Hg (THg) concentrations range from 10 to 500 ng/l and are lower than the 1000 ng/l threshold value for human health protection fixed by the World Health Organization [WHO (1993): WHO Guidelines for Drinking Water Quality- http://www.who.int/water_sanitation_health/GDWQ/index.htlm]. Positive co-variations of (THg) with sulphate indicate that Hg-SO 4-rich acid groundwaters receive a direct input of magmatic/hydrothermal gases carrying mercury as Hg 0(gas). Increasing THg in a volcanic aquifer could thus be a sensitive tracer of magmatic gas input prior to an eruption. Since the complex behaviour and toxicity of mercury in waters depend on its chemical speciation, we carefully determined the different aqueous forms of this element in our samples. We find that dissolved elemental Hg 0(aq) and particulate-bound Hg (Hg P) widely prevail in volcanic aquifers, in proportions that highlight the efficiency of Hg adsorption onto colloidal particles. Moreover, we observe that dissolved Hg 0aq and Hg(II) forms coexist in comparable amount in most of the waters, in stark contrast to the results of thermodynamic equilibrium modelling. Therefore, chemical equilibrium between dissolved mercury species in volcanic waters is either prevented by natural kinetic effects or not preserved in collected waters due to sampling/storage artefacts. Finally, we

AQUIFER IN AJAOKUTA, SOUTHWESTERN NIGERIA

African Journals Online (AJOL)

2005-03-08

Mar 8, 2005 ... To establish the feasibility of water supply in a basement complex area ofAjaokuta, Southwestern Nigeria, pumping test results were used to investigate the storage properties and groundwater potential of the aquifer. The aquifer system consists of weathered and weathered/fractured zone of decomposed ...

Straddle-packer aquifer test analyses of the Snake River Plain aquifer at the Idaho National Engineering Laboratory

International Nuclear Information System (INIS)

Johnson, G.S.; Frederick, D.B.

1997-01-01

The State of Idaho INEL Oversight Program, with the University of Idaho, Idaho State University, Boise State University, and the Idaho Geologic Survey, used a straddle-packer system to investigate vertical variations in characteristics of the Snake River Plain aquifer at the Idaho National Engineering Laboratory in southeast Idaho. Sixteen single-well aquifer tests were conducted on.isolated intervals in three observation wells. Each of these wells has approximately 200 feet of open borehole below the water table, penetrating the E through G and I basalt flow groups and interbedded sediments of the Snake River Plain aquifer. The success of the aquifer tests was limited by the inability to induce measurable drawdown in several zones. Time-drawdown data from aquifer tests were matched to type curves for 8 of the 16 zones tested. A single aquifer test at the water table exhibited greater curvature than those at depth. The increased degree of curvature suggests an unconfined response and resulted in an estimate of specific yield of 0.03. Aquifer tests below the water table generally yielded time-drawdown graphs with a rapid initial response followed by constant drawdown throughout the duration of the tests; up to several hours in length. The rapid initial response implies that the aquifer responds as a confined system during brief pumping periods. The nearly constant drawdown suggests a secondary source of water, probably vertical flow from overlying and underlying aquifer layers. Three analytical models were applied for comparison to the conceptual model and to provide estimates of aquifer properties. This, Hantush-Jacob leaky aquifer, and the Moench double-porosity fractured rock models were fit to time-drawdown data. The leaky aquifer type curves of Hantush and Jacob generally provided the best match to observed drawdown. A specific capacity regression equation was also used to estimate hydraulic conductivity

Aquifer geochemistry at potential aquifer storage and recovery sites in coastal plain aquifers in the New York city area, USA

Science.gov (United States)

Brown, C.J.; Misut, P.E.

2010-01-01

The effects of injecting oxic water from the New York city (NYC) drinking-water supply and distribution system into a nearby anoxic coastal plain aquifer for later recovery during periods of water shortage (aquifer storage and recovery, or ASR) were simulated by a 3-dimensional, reactive-solute transport model. The Cretaceous aquifer system in the NYC area of New York and New Jersey, USA contains pyrite, goethite, locally occurring siderite, lignite, and locally varying amounts of dissolved Fe and salinity. Sediment from cores drilled on Staten Island and western Long Island had high extractable concentrations of Fe, Mn, and acid volatile sulfides (AVS) plus chromium-reducible sulfides (CRS) and low concentrations of As, Pb, Cd, Cr, Cu and U. Similarly, water samples from the Lloyd aquifer (Cretaceous) in western Long Island generally contained high concentrations of Fe and Mn and low concentrations of other trace elements such as As, Pb, Cd, Cr, Cu and U, all of which were below US Environmental Protection Agency (USEPA) and NY maximum contaminant levels (MCLs). In such aquifer settings, ASR operations can be complicated by the oxidative dissolution of pyrite, low pH, and high concentrations of dissolved Fe in extracted water.The simulated injection of buffered, oxic city water into a hypothetical ASR well increased the hydraulic head at the well, displaced the ambient groundwater, and formed a spheroid of injected water with lower concentrations of Fe, Mn and major ions in water surrounding the ASR well, than in ambient water. Both the dissolved O2 concentrations and the pH of water near the well generally increased in magnitude during the simulated 5-a injection phase. The resultant oxidation of Fe2+ and attendant precipitation of goethite during injection provided a substrate for sorption of dissolved Fe during the 8-a extraction phase. The baseline scenario with a low (0.001M) concentration of pyrite in aquifer sediments, indicated that nearly 190% more water

Depth and temporal variations in water quality of the Snake River Plain aquifer in well USGS-59 near the Idaho Chemical Processing Plant at the Idaho National Engineering and Environmental Laboratory

International Nuclear Information System (INIS)

Frederick, D.B.; Johnson, G.S.

1997-03-01

In-situ measurements of the specific conductance and temperature of ground water in the Snake River Plain aquifer were collected in observation well USGS-59 near the Idaho Chemical Processing Plant at the Idaho National Engineering and Environmental Laboratory. These parameters were monitored at various depths in the aquifer from October 1994 to August 1995. The specific conductance of ground water in well USGS-59, as measured in the borehole, ranged from about 450 to 900 microS/cm at standard temperature (25 C). The pumping cycle of the production wells at the Idaho Chemical Processing Plant causes changes in borehole circulation patterns, and as a result the specific conductance of ground water at some depths in the well varies by up to 50% over a period of about 14 hours. However, these variations were not observed at all depths, or during each pumping cycle. The temperature of ground water in the well was typically between 12.8 and 13.8 C. The results of this study indicate that temporal variations in specific conductance of the ground water at this location are caused by an external stress on the aquifer--pumping of a production well approximately 4,000 feet away. These variations are believed to result from vertical stratification of water quality in the aquifer and a subsequent change in intrawell flow related to pumping. When sampling techniques that do not induce a stress on the aquifer (i.e., thief sampling) are used, knowledge of external stresses on the system at the time of sampling may aid in the interpretation of geochemical data

Hydrogeochemical study of water in some aquifers of the Estado de Mexico; Estudio hidrogeoquimico de agua de algunos manantiales del Estado de Mexico

Energy Technology Data Exchange (ETDEWEB)

Pena, P.; Lopez, A.; Balcazar, M.; Flores, J.H.; Cardenas, S. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Schubert, M. [UFZ Centre for Environmental Research Leipzig-Halle GMBH, Permoser Str. 15, 04318 Leipzig (Germany)

2005-07-01

The National Institute of Nuclear Research of Mexico (ININ), has developed a technique that allows to study the association of recharge mechanisms, residence times of the water in the aquifers, as well as the local lithology and the geochemical parameters. The viability of this technique was proven on November 2004 in the aquifers (La Perita, El Tunel y El Pedregal) located in the Asuncion Tepexoyuca, Estado de Mexico. It was observed that so much the aquifer El Tunel like La Perita are used for the human consumption, the aquifer of El Pedregal is used for the fish cultivation. The studies were carried out during March 2003 to November 2004. In the aquifer La Perita the maximum values of the radon concentration (0.76 Bq L{sup -1}) they were observed in the summertime time (December). In the spring El Tunel the maximum values of the radon concentration (4.08 Bq L{sup -1}) they were observed in the rainy season (September) this increment can be due to the contributions of the recharge of aquifers that it allows the haulage of the radon of other alternating roads of infiltration of the rain water. Of the physicochemical and radiochemical analyses carried out in the water samples of the studied aquifers, it is deduced that they are waters of good quality since for the human consumption since that they are inside on the maximum permissible limits as for their potability according to national and international standards. Likewise it was observed that the water of the aquifers is a single aquifer, since that its differences they due to the time of permanency of the water inside the aquifer. The classification of the underground water deduced that it is calcic and/or magnesic bi carbonated water belonging to the type of meteoric waters of recent infiltration. (Author)

Model Simulations of a Field Experiment on Cation Exchange-affected Multicomponent Solute Transport in a Sandy Aquifer

DEFF Research Database (Denmark)

Bjerg, Poul Løgstrup; Ammentorp, Hans Christian; Christensen, Thomas Højlund

1993-01-01

A large-scale and long-term field experiment on cation exchange in a sandy aquifer has been modelled by a three-dimensional geochemical transport model. The geochemical model includes cation-exchange processes using a Gaines-Thomas expression, the closed carbonate system and the effects of ionic...... by batch experiments and by the composition of the cations on the exchange complex. Potassium showed a non-ideal exchange behaviour with K&z.sbnd;Ca selectivity coefficients indicating dependency on equivalent fraction and K+ concentration in the aqueous phase. The model simulations over a distance of 35 m...... and a period of 250 days described accurately the observed attenuation of Na and the expelled amounts of Ca and Mg. Also, model predictions of plateau zones, formed by interaction with the background groundwater, in general agreed satisfactorily with the observations. Transport of K was simulated over a period...

Alluvial Aquifer

Data.gov (United States)

Kansas Data Access and Support Center — This coverage shows the extents of the alluvial aquifers in Kansas. The alluvial aquifers consist of unconsolidated Quaternary alluvium and contiguous terrace...

Geochemical exploration for uranium

International Nuclear Information System (INIS)

1988-01-01

This Technical Report is designed mainly to introduce the methods and techniques of uranium geochemical exploration to exploration geologists who may not have had experience with geochemical exploration methods in their uranium programmes. The methods presented have been widely used in the uranium exploration industry for more than two decades. The intention has not been to produce an exhaustive, detailed manual, although detailed instructions are given for a field and laboratory data recording scheme and a satisfactory analytical method for the geochemical determination of uranium. Rather, the intention has been to introduce the concepts and methods of uranium exploration geochemistry in sufficient detail to guide the user in their effective use. Readers are advised to consult general references on geochemical exploration to increase their understanding of geochemical techniques for uranium

Differentiated spring behavior under changing hydrological conditions in an alpine karst aquifer

Science.gov (United States)

Filippini, Maria; Squarzoni, Gabriela; De Waele, Jo; Fiorucci, Adriano; Vigna, Bartolomeo; Grillo, Barbara; Riva, Alberto; Rossetti, Stefano; Zini, Luca; Casagrande, Giacomo; Stumpp, Christine; Gargini, Alessandro

2018-01-01

Limestone massifs with a high density of dolines form important karst aquifers in most of the Alps, often with groundwater circulating through deep karst conduits and water coming out of closely spaced springs with flow rates of over some cubic meters per second. Although several hydrogeological studies and tracing experiments were carried out in many of these carbonate mountains in the past, the hydrogeology of most of these karst aquifers is still poorly known. Geological, hydrodynamic and hydrochemical investigations have been carried out in one of the most representative of these areas (Cansiglio-Monte Cavallo, NE Italy) since spring 2015, in order to enhance the knowledge on this important type of aquifer system. Additionally, a cave-to-spring multitracer test was carried out in late spring 2016 by using three different fluorescent tracers. This hydrogeological study allowed: 1) gathering new detailed information on the geological and tectonic structure of such alpine karst plateau; 2) defining discharge rates of the three main springs (Gorgazzo, Santissima, and Molinetto) by constructing rating curves; 3) understanding the discharging behavior of the system with respect to different recharge conditions; 4) better defining the recharge areas of the three springs. The three nearby springs (the spring front stretches over 5 km), that drain the investigated karst aquifer system, show different behaviors with respect to changing discharge conditions, demonstrating this aquifer to be divided in partially independent drainage systems under low-flow conditions, when their chemistry is clearly differentiated. Under high-flow conditions, waters discharging at all springs show more similar geochemical characteristics. The combination of geochemistry, hydrodynamic monitoring and dye tracing tests has shown that the three springs have different recharge areas. The study points out that even closely spaced karst springs, that apparently drain the same karst mountain, can

Strontium isotope geochemistry of groundwater in the central part of the Dakota (Great Plains) aquifer, USA

International Nuclear Information System (INIS)

Gosselin, David C.; Edwin Harvey, F.; Frost, Carol; Stotler, Randy; Allen Macfarlane, P.

2004-01-01

The Dakota aquifer of the central and eastern Great Plains of the United States is an important source of water for municipal supplies, irrigation and industrial use. Although the regional flow system can be characterized generally as east to northeasterly from the Rocky Mountains towards the Missouri River, locally the flow systems are hydrologically complex. This study uses Sr isotopic data from groundwater and leached aquifer samples to document the complex subsystems within the Dakota aquifer in Nebraska and Kansas. The interaction of groundwater with the geologic material through which it flows has created spatial patterns in the isotopic measurements that are related to: long-term water-rock interaction, during which varying degrees of isotopic equilibrium between water and rock has been achieved; and the alteration of NaCl fluids by water-rock interaction. Specifically, Sr isotopic data distinguish brines from Kansas and western Nebraska from those in eastern Nebraska: the former are interpreted to reflect interaction with Permian rocks, whereas the latter record interaction with Pennsylvanian rocks. The Sr isotopic composition of groundwater from other parts of Nebraska and Kansas are a function of the dynamic interaction between groundwater and unlithified sediments (e.g., glacial till and loess), followed by interaction with oxidized and unoxidized sediments within the Dakota Formation. This study illustrates the power of combining Sr chemistry with more conventional geochemical data to obtain a more complete understanding of groundwater flow systems within regional aquifer systems where extensive monitoring networks do not exist

Reduced-Order Model for the Geochemical Impacts of Carbon Dioxide, Brine and Trace Metal Leakage into an Unconfined, Oxidizing Carbonate Aquifer, Version 2.1

Energy Technology Data Exchange (ETDEWEB)

Bacon, Diana H.

2013-03-31

The National Risk Assessment Partnership (NRAP) consists of 5 U.S DOE national laboratories collaborating to develop a framework for predicting the risks associated with carbon sequestration. The approach taken by NRAP is to divide the system into components, including injection target reservoirs, wellbores, natural pathways including faults and fractures, groundwater and the atmosphere. Next, develop a detailed, physics and chemistry-based model of each component. Using the results of the detailed models, develop efficient, simplified models, termed reduced order models (ROM) for each component. Finally, integrate the component ROMs into a system model that calculates risk profiles for the site. This report details the development of the Groundwater Geochemistry ROM for the Edwards Aquifer at PNNL. The Groundwater Geochemistry ROM for the Edwards Aquifer uses a Wellbore Leakage ROM developed at LANL as input. The detailed model, using the STOMP simulator, covers a 5x8 km area of the Edwards Aquifer near San Antonio, Texas. The model includes heterogeneous hydraulic properties, and equilibrium, kinetic and sorption reactions between groundwater, leaked CO2 gas, brine, and the aquifer carbonate and clay minerals. Latin Hypercube sampling was used to generate 1024 samples of input parameters. For each of these input samples, the STOMP simulator was used to predict the flux of CO2 to the atmosphere, and the volume, length and width of the aquifer where pH was less than the MCL standard, and TDS, arsenic, cadmium and lead exceeded MCL standards. In order to decouple the Wellbore Leakage ROM from the Groundwater Geochemistry ROM, the response surface was transformed to replace Wellbore Leakage ROM input parameters with instantaneous and cumulative CO2 and brine leakage rates. The most sensitive parameters proved to be the CO2 and brine leakage rates from the well, with equilibrium coefficients for calcite and dolomite, as well as the number of illite and kaolinite

A Geochemical Mass-Balance Method for Base-Flow Separation, Upper Hillsborough River Watershed, West-Central Florida, 2003-2005 and 2009

Science.gov (United States)

Kish, G.R.; Stringer, C.E.; Stewart, M.T.; Rains, M.C.; Torres, A.E.

2010-01-01

Geochemical mass-balance (GMB) and conductivity mass-balance (CMB) methods for hydrograph separation were used to determine the contribution of base flow to total stormflow at two sites in the upper Hillsborough River watershed in west-central Florida from 2003-2005 and at one site in 2009. The chemical and isotopic composition of streamflow and precipitation was measured during selected local and frontal low- and high-intensity storm events and compared to the geochemical and isotopic composition of groundwater. Input for the GMB method included cation, anion, and stable isotope concentrations of surface water and groundwater, whereas input for the CMB method included continuous or point-sample measurement of specific conductance. The surface water is a calcium-bicarbonate type water, which closely resembles groundwater geochemically, indicating that much of the surface water in the upper Hillsborough River basin is derived from local groundwater discharge. This discharge into the Hillsborough River at State Road 39 and at Hillsborough River State Park becomes diluted by precipitation and runoff during the wet season, but retains the calcium-bicarbonate characteristics of Upper Floridan aquifer water. Field conditions limited the application of the GMB method to low-intensity storms but the CMB method was applied to both low-intensity and high-intensity storms. The average contribution of base flow to total discharge for all storms ranged from 31 to 100 percent, whereas the contribution of base flow to total discharge during peak discharge periods ranged from less than 10 percent to 100 percent. Although calcium, magnesium, and silica were consistent markers of Upper Floridan aquifer chemistry, their use in calculating base flow by the GMB method was limited because the frequency of point data collected in this study was not sufficient to capture the complete hydrograph from pre-event base-flow to post-event base-flow concentrations. In this study, pre-event water

Geochemical sensitivity analysis: Identification of important geochemical parameters for performance assessment studies

International Nuclear Information System (INIS)

Siegel, M.; Guzowski, R.; Rechard, R.; Erickson, K.

1986-01-01

The EPA Standard for geologic disposal of high level waste requires demonstration that the cumulative discharge of individual radioisotopes over a 10,000 year period at points 5 kilometers from the engineered barrier system will not exceed the limits prescribed in 40 CFR Part 191. The roles of the waste package, engineered facility, hydrogeology and geochemical processes in limiting radionuclide releases all must be considered in calculations designed to assess compliance of candidate repositories with the EPA Standard. In this talk, they will discuss the geochemical requirements of calculations used in these compliance assessments. In addition, they will describe the complementary roles of (1) simple models designed to bound the radionuclide discharge over the widest reasonable range of geochemical conditions and scenarios and (2) detailed geochemical models which can provide insights into the actual behavior of the radionuclides in the ground water. Finally, they will discuss development of sensitivity/uncertainty techniques designed to identify important site-specific geochemical parameters and processes using data from a basalt formation

Inverse Modeling of Water-Rock-CO2 Batch Experiments: Potential Impacts on Groundwater Resources at Carbon Sequestration Sites.

Science.gov (United States)

Yang, Changbing; Dai, Zhenxue; Romanak, Katherine D; Hovorka, Susan D; Treviño, Ramón H

2014-01-01

This study developed a multicomponent geochemical model to interpret responses of water chemistry to introduction of CO2 into six water-rock batches with sedimentary samples collected from representative potable aquifers in the Gulf Coast area. The model simulated CO2 dissolution in groundwater, aqueous complexation, mineral reactions (dissolution/precipitation), and surface complexation on clay mineral surfaces. An inverse method was used to estimate mineral surface area, the key parameter for describing kinetic mineral reactions. Modeling results suggested that reductions in groundwater pH were more significant in the carbonate-poor aquifers than in the carbonate-rich aquifers, resulting in potential groundwater acidification. Modeled concentrations of major ions showed overall increasing trends, depending on mineralogy of the sediments, especially carbonate content. The geochemical model confirmed that mobilization of trace metals was caused likely by mineral dissolution and surface complexation on clay mineral surfaces. Although dissolved inorganic carbon and pH may be used as indicative parameters in potable aquifers, selection of geochemical parameters for CO2 leakage detection is site-specific and a stepwise procedure may be followed. A combined study of the geochemical models with the laboratory batch experiments improves our understanding of the mechanisms that dominate responses of water chemistry to CO2 leakage and also provides a frame of reference for designing monitoring strategy in potable aquifers.

Thermo-hydro-chemical performance assessment of CO2 storage in saline aquifer

International Nuclear Information System (INIS)

Le Gallo, Y.; Trenty, L.; Michel, A.

2007-01-01

Research and development methodologies for the storage of CO 2 in geological formation are in developing over the last 10 years. In this context, numerical simulators are the practical tools to understand the physical processes involved by acid gas injection and evaluate the long term stability of the storage. CO 2 storage models can be seen as a mix between two types of models: a reservoir model coupling multiphase flow in porous media with local phase equilibrium and a hydrogeochemical model coupling transport in aqueous phase with local chemical equilibrium and kinetic reaction laws. A 3D-multiphase model, COORES, was built to assess the influence of different driving forces both hydrodynamic and geomechanics as well as geochemical on the CO 2 plume behavior during injection and storage (1000 years). Different coupling strategies were used to model these phenomena: - pressure, temperature and diffusion are solved implicitly for better numerical stability; - geochemical reactions involve heterogeneous kinetically-controlled reactions between the host rock and the CO 2 -rich aqueous phase which imply an implicit coupling with fluid flow; From the assumed initial mineral composition (6 minerals), aqueous species (10 chemical elements and 37 aqueous species), the geochemical alteration of the host rocks (sand and shale) is directly linked with the CO 2 plume evolution. A performance assessment using an experimental design approach is used to quantify the different driving forces and parameter influences. In the case of CO 2 injection in a saline quartz rich aquifer used to illustrate the model capabilities, the geochemical changes of the host rock have a small influence on the CO 2 distribution at the end of storage life (here 1000 years) compared to the other hydrodynamic mechanisms: free CO 2 (gas or supercritical), or trapped (capillary and in-solution). (authors)

Carbon isotopes of dissolved inorganic carbon reflect utilization of different carbon sources by microbial communities in two limestone aquifer assemblages

Directory of Open Access Journals (Sweden)

M. E. Nowak

2017-08-01

Full Text Available Isotopes of dissolved inorganic carbon (DIC are used to indicate both transit times and biogeochemical evolution of groundwaters. These signals can be complicated in carbonate aquifers, as both abiotic (i.e., carbonate equilibria and biotic factors influence the δ13C and 14C of DIC. We applied a novel graphical method for tracking changes in the δ13C and 14C of DIC in two distinct aquifer complexes identified in the Hainich Critical Zone Exploratory (CZE, a platform to study how water transport links surface and shallow groundwaters in limestone and marlstone rocks in central Germany. For more quantitative estimates of contributions of different biotic and abiotic carbon sources to the DIC pool, we used the NETPATH geochemical modeling program, which accounts for changes in dissolved ions in addition to C isotopes. Although water residence times in the Hainich CZE aquifers based on hydrogeology are relatively short (years or less, DIC isotopes in the shallow, mostly anoxic, aquifer assemblage (HTU were depleted in 14C compared to a deeper, oxic, aquifer complex (HTL. Carbon isotopes and chemical changes in the deeper HTL wells could be explained by interaction of recharge waters equilibrated with post-bomb 14C sources with carbonates. However, oxygen depletion and δ13C and 14C values of DIC below those expected from the processes of carbonate equilibrium alone indicate considerably different biogeochemical evolution of waters in the upper aquifer assemblage (HTU wells. Changes in 14C and 13C in the upper aquifer complexes result from a number of biotic and abiotic processes, including oxidation of 14C-depleted OM derived from recycled microbial carbon and sedimentary organic matter as well as water–rock interactions. The microbial pathways inferred from DIC isotope shifts and changes in water chemistry in the HTU wells were supported by comparison with in situ microbial community structure based on 16S rRNA analyses. Our findings

Simulation of reactive geochemical transport in groundwater using a semi-analytical screening model

Science.gov (United States)

McNab, Walt W.

1997-10-01

A reactive geochemical transport model, based on a semi-analytical solution to the advective-dispersive transport equation in two dimensions, is developed as a screening tool for evaluating the impact of reactive contaminants on aquifer hydrogeochemistry. Because the model utilizes an analytical solution to the transport equation, it is less computationally intensive than models based on numerical transport schemes, is faster, and it is not subject to numerical dispersion effects. Although the assumptions used to construct the model preclude consideration of reactions between the aqueous and solid phases, thermodynamic mineral saturation indices are calculated to provide qualitative insight into such reactions. Test problems involving acid mine drainage and hydrocarbon biodegradation signatures illustrate the utility of the model in simulating essential hydrogeochemical phenomena.

Palaeoclimatic trends deduced from the hydrochemistry of a Triassic sandstone aquifer, United Kingdom

International Nuclear Information System (INIS)

Bath, A.H.; Edmunds, W.M.; Andrews, J.N.

1979-01-01

A detailed geochemical study (elemental, isotopic and dissolved inert gases) of unconfined and confined sections of the Triassic non-marine sandstone aquifer in eastern England has been undertaken. Aspects of the recharge history of this aquifer over the past 40,000 years are revealed by examination of the data. 14 C activity and delta 13 C values show downgradient decrease and increase, respectively, the latter from -12 to -13 per mille (PDB) at outcrop to -8.5 per mille in deep confined groundwaters, indicating a continuing reaction between water and carbonate mineral phases. Although the bulk carbonate contained in sandstone samples gives delta 13 C around -7 per mille, modelling of the carbon isotopic evolution and consideration of the resulting 14 C age corrections suggest that a carbonate with delta 13 C closer to 0 per mille has played a major role in at least the earlier stages of hydrochemical evolution. The corrected radiocarbon age ranges, generated by the computer program WATEQF-ISOTOP, are used as a framework in which the palaeo-environmental information from oxygen and hydrogen isotope data, inert gas contents, and chloride levels are discussed. The measurement of dissolved helium levels demonstrates an excess of 4 He in many samples, which correlates with radiocarbon ages. The assumption of bulk chemical and physical properties for the aquifer rock allows independent 'excess 4 He' ages to be computed, which are mostly in excess of the corrected 14 C ages. The trend of delta 18 O is from about -8 per mille at outcrop to -9.7 per mille (SMOW) downgradient, which is significantly more depleted than has been found in previous studies of UK basins. The delta 2 H and delta 18 O values are related by the regression line delta 2 H=6.6delta 18 O+1; data from other UK studies also lie close to this trend

Temporal and spatial variations in groundwater quality resulting from policy-induced reductions in nitrate leaching to the Rabis Creek aquifer, Denmark

Science.gov (United States)

Jessen, Søren; Engesgaard, Peter; Thorling, Lærke; Müller, Sascha; Leskelä, Jari; Postma, Dieke

2016-04-01

-gradient along the transect. During the 25 year monitoring period the redoxcline has moved by one to a few decimeters, as controlled by the aquifer sediment's pyrite content. Further, the data indicate that no zero-valent sulfur is precipitated during pyrite oxidation in the aquifer, while most of the pyritic iron is precipitated. Nickel (Ni2+) is released at the redoxcline resulting in concentrations more than twice the 20 μg/L Danish drinking water limit. The data clearly indicate that this Ni2+ contamination can be ascribed to the agricultural nitrate loading and would not occur under natural conditions. A 2D reactive transport model was constructed (PHAST 3) to simulate the temporal and spatial development in nitrate and sulfate concentrations in the aquifer while taking into account effects of dispersion. The model predictions indicate that sulfate concentrations, despite dispersive mixing, is still increasing along down-gradient stretches of the aquifer, where flow paths surface from the deeper up-gradient part of the aquifer, to eventually discharge into the Rabis Creek.

Assessing the recharge of a coastal aquifer using physical observations, tritium, groundwater chemistry and modelling.

Science.gov (United States)

Santos, Isaac R; Zhang, Chenming; Maher, Damien T; Atkins, Marnie L; Holland, Rodney; Morgenstern, Uwe; Li, Ling

2017-02-15

Assessing recharge is critical to understanding groundwater and preventing pollution. Here, we investigate recharge in an Australian coastal aquifer using a combination of physical, modelling and geochemical techniques. We assess whether recharge may occur through a pervasive layer of floodplain muds that was initially hypothesized to be impermeable. At least 59% of the precipitation volume could be accounted for in the shallow aquifer using the water table fluctuation method during four significant recharge events. Precipitation events rates were estimated in the area underneath the floodplain clay layer rather than in the sandy area. A steady-state chloride method implied recharge rates of at least 200mm/year (>14% of annual precipitation). Tritium dating revealed long term net vertical recharge rates ranging from 27 to 114mm/year (average 58mm/year) which were interpreted as minimum net long term recharge. Borehole experiments revealed more permeable conditions and heterogeneous infiltration rates when the floodplain soils were dry. Wet conditions apparently expand floodplain clays, closing macropores and cracks that act as conduits for groundwater recharge. Modelled groundwater flow paths were consistent with tritium dating and provided independent evidence that the clay layer does not prevent local recharge. Overall, all lines of evidence demonstrated that the coastal floodplain muds do not prevent the infiltration of rainwater into the underlying sand aquifer, and that local recharge across the muds was widespread. Therefore, assuming fine-grained floodplain soils prevent recharge and protect underlying aquifers from pollution may not be reasonable. Copyright © 2016 Elsevier B.V. All rights reserved.

Results of geochemical and mineralogical studies on uranium in Zechstein copper-bearing strata from Lubin-Polkowice area

International Nuclear Information System (INIS)

Bareja, E.

1977-01-01

The paper presents the results of geochemical and mineralogical studies on uranium in Zechstein copper-bearing strata from the Lubin-Polkowice area. It was found that particular lithofacial varietes of Zechstein copper-bearing strata are characterized by different concentration of uranium. The mineralogical studies made possible determination of the nature of uranium mineralization and the interdependence between uranium and lithology of copper-bearing strata. An interesting uranium mineralization was found in tectonic breccias which yield black blende and schroeckingerite as well as calcite, gypsum, pyrite, hematite and geothite. Secondary minerals such as schroeckingerite and geothite evidence intense weathering processes acting in the copper deposit. The highest value of geochemical background of uranium in the copper-bearing series is displayed by basel copper-bearing shales (so called pitch-black shales) - 68.10 x 10 -40 /0 U. Statistical distribution of that element is unimodal. Distribution of uranium is polymodal in basal sandstones of the copper-bearing series. The geochemical background of red-coloured sandstones (Rotliegendes) is low, equalling 0.39 x 10 40 /0 U, whilst that of gray-coloured sandstones (Zechstein) - 2.32 x 10 -40 /0 U. An anomallous population (344.0 x 10 -40 /0 U) found in the case of gray sandstones of the Lubin-Polkowice area evidences the effects of secondary processes on concentration of uranium. In sandstones occur black blende, carburanes as well as calcite, hematite and goethite. A bimodal distribution of uranium was found in carbonate series. Limestones are characterized by low value of geochemical background (Dsub(x1) = 0.78 x 10 -40 /0 U) whilst dolomites by markedly higher values of the background (Dsub(x2) = 2.73 x 10 -40 /0 U). (author)

Comment on An Alternative View on the Origin of Chemical and Isotopic Patterns in Groundwater From the Milk River Aquifer, Canada by M.J. Hendry and F.W. Schwartz

International Nuclear Information System (INIS)

Phillips, F.M.; Knowlton, R.G.; Bentley, H.W.

1990-01-01

The Milk River aquifer in southern Alberta combines apparently simple, classical confined aquifer hydrodynamics with somewhat enigmatic groundwater geochemistry of conservative solutes. Over the past 10 years, five major papers have focused on the geochemistry of Milk River aquifer groundwater. Most recently, Hendry and Schwartz (1988) have proposed a different mechanism, aquitard diffusion, to explain the Milk River geochemistry. They described and evaluated previously proposed geochemical processes, especially ion filtration. Hendry and Schwartz (1988) concluded that ion filtration and the other proposed mechanisms were not supported by the data. They then described the aquitard diffusion mechanism and used a simple analytical model to simulate observed aquifer trends in Cl - and 18 O. From the results of this exercise they concluded that diffusion from the aquitards was controlling the solute distributions in the aquifer. Finally, they interpreted previously published 36 Cl data and new profiles of Cl - in the aquitards in terms of the diffusion model. Upon review, the authors do not find the arguments against ion filtration to be as damaging as Hendry and Schwartz indicate, nor do they find the evidence for aquitard diffusion to be as persuasive. In this study they will first evaluate Hendry and Schwartz's arguments against ion filtration, then they will review the arguments in favor of aquitard diffusion, and finally the authors will address the implications for the interpretation of the vertical Cl - profiles and the 36 Cl data

Hydrological controls on transient aquifer storage in a karst watershed

Science.gov (United States)

Spellman, P.; Martin, J.; Gulley, J. D.

2017-12-01

While surface storage of floodwaters is well-known to attenuate flood peaks, transient storage of floodwaters in aquifers is a less recognized mechanism of flood peak attenuation. The hydraulic gradient from aquifer to river controls the magnitude of transient aquifer storage and is ultimately a function of aquifer hydraulic conductivity, and effective porosity. Because bedrock and granular aquifers tend to have lower hydraulic conductivities and porosities, their ability to attenuate flood peaks is generally small. In karst aquifers, however, extensive cave systems create high hydraulic conductivities and porosities that create low antecedent hydraulic gradients between aquifers and rivers. Cave springs can reverse flow during high discharges in rivers, temporarily storing floodwaters in the aquifer thus reducing the magnitude of flood discharge downstream. To date however, very few studies have quantified the magnitude or controls of transient aquifer storage in karst watersheds. We therefore investigate controls on transient aquifer storage by using 10 years of river and groundwater data from the Suwannee River Basin, which flows over the karstic upper Floridan aquifer in north-central Florida. We use multiple linear regression to compare the effects of three hydrological controls on the magnitude of transient aquifer storage: antecedent stage, recharge and slope of hydrograph rise. We show the dominant control on transient aquifer storage is antecedent stage, whereby lower stages result in greater magnitudes of transient aquifer storage. Our results suggest that measures of groundwater levels prior to an event can be useful in determining whether transient aquifer storage will occur and may provide a useful metric for improving predictions of flood magnitudes.

Up-Scaling Geochemical Reaction Rates for Carbon Dioxide (CO2) in Deep Saline Aquifers

Energy Technology Data Exchange (ETDEWEB)

Peters, Catherine A

2013-02-28

Geochemical reactions in deep subsurface environments are complicated by the consolidated nature and mineralogical complexity of sedimentary rocks. Understanding the kinetics of these reactions is critical to our ability to make long-term predictions about subsurface processes such as pH buffering, alteration in rock structure, permeability changes, and formation of secondary precipitates. In this project, we used a combination of experiments and numerical simulation to bridge the gap between our knowledge of these reactions at the lab scale and rates that are meaningful for modeling reactive transport at core scales. The focus is on acid-driven mineral dissolution, which is specifically relevant in the context of CO2-water-rock interactions in geological sequestration of carbon dioxide. The project led to major findings in three areas. First, we modeled reactive transport in pore-network systems to investigate scaling effects in geochemical reaction rates. We found significant scaling effects when CO2 concentrations are high and reaction rates are fast. These findings indicate that the increased acidity associated with geological sequestration can generate conditions for which proper scaling tools are yet to be developed. Second, we used mathematical modeling to investigate the extent to which SO2, if co-injected with CO2, would acidify formation brines. We found that there exist realistic conditions in which the impact on brine acidity will be limited due to diffusion rate-limited SO2 dissolution from the CO2 phase, and the subsequent pH shift may also be limited by the lack of availability of oxidants to produce sulfuric acid. Third, for three Viking sandstones (Alberta sedimentary basin, Canada), we employed backscattered electron microscopy and energy dispersive X-ray spectroscopy to statistically characterize mineral contact with pore space. We determined that for reactive minerals in sedimentary consolidated rocks, abundance alone is not a good predictor of

Probabilistic, sediment-geochemical parameterisation of the groundwater compartment of the Netherlands for spatially distributed, reactive transport modelling

Science.gov (United States)

Janssen, Gijs; Gunnink, Jan; van Vliet, Marielle; Goldberg, Tanya; Griffioen, Jasper

2017-04-01

Pollution of groundwater aquifers with contaminants as nitrate is a common problem. Reactive transport models are useful to predict the fate of such contaminants and to characterise the efficiency of mitigating or preventive measures. Parameterisation of a groundwater transport model on reaction capacity is a necessary step during building the model. Two Dutch, national programs are combined to establish a methodology for building a probabilistic model on reaction capacity of the groundwater compartment at the national scale: the Geological Survey program and the NHI Netherlands Hydrological Instrument program. Reaction capacity is considered as a series of geochemical characteristics that control acid/base condition, redox condition and sorption capacity. Five primary reaction capacity variables are characterised: 1. pyrite, 2. non-pyrite, reactive iron (oxides, siderite and glauconite), 3. clay fraction, 4. organic matter and 5. Ca-carbonate. Important reaction capacity variables that are determined by more than one solid compound are also deduced: 1. potential reduction capacity (PRC) by pyrite and organic matter, 2. cation-exchange capacity (CEC) by organic matter and clay content, 3. carbonate buffering upon pyrite oxidation (CPBO) by carbonate and pyrite. Statistical properties of these variables are established based on c. 16,000 sediment geochemical analyses. The first tens of meters are characterised based on 25 regions using combinations of lithological class and geological formation as strata. Because of both less data and more geochemical uniformity, the deeper subsurface is characterised in a similar way based on 3 regions. The statistical data is used as input in an algoritm that probabilistically calculates the reaction capacity per grid cell. First, the cumulative frequency distribution (cfd) functions are calculated from the statistical data for the geochemical strata. Second, all voxel cells are classified into the geochemical strata. Third, the

Fertilizers mobilization in alluvial aquifer: laboratory experiments

Science.gov (United States)

Mastrocicco, M.; Colombani, N.; Palpacelli, S.

2009-02-01

In alluvial plains, intensive farming with conspicuous use of agrochemicals, can cause land pollution and groundwater contamination. In central Po River plain, paleo-channels are important links between arable lands and the underlaying aquifer, since the latter is often confined by clay sediments that act as a barrier against contaminants migration. Therefore, paleo-channels are recharge zones of particular interest that have to be protected from pollution as they are commonly used for water supply. This paper focuses on fertilizer mobilization next to a sand pit excavated in a paleo-channel near Ferrara (Italy). The problem is approached via batch test leaking and columns elution of alluvial sediments. Results from batch experiments showed fast increase in all major cations and anions, suggesting equilibrium control of dissolution reactions, limited availability of solid phases and geochemical homogeneity of samples. In column experiments, early elution and tailing of all ions breakthrough was recorded due to preferential flow paths. For sediments investigated in this study, dispersion, dilution and chemical reactions can reduce fertilizers at concentration below drinking standards in a reasonable time frame, provided fertilizer loading is halted or, at least, reduced. Thus, the definition of a corridor along paleo-channels is recommended to preserve groundwater quality.

Aquifer Storage Recovery (ASR) of chlorinated municipal drinking water in a confined aquifer

Science.gov (United States)

Izbicki, John A.; Petersen, Christen E.; Glotzbach, Kenneth J.; Metzger, Loren F.; Christensen, Allen H.; Smith, Gregory A.; O'Leary, David R.; Fram, Miranda S.; Joseph, Trevor; Shannon, Heather

2010-01-01

About 1.02 x 106 m3 of chlorinated municipal drinking water was injected into a confined aquifer, 94-137 m below Roseville, California, between December 2005 and April 2006. The water was stored in the aquifer for 438 days, and 2.64 x 106 m3 of water were extracted between July 2007 and February 2008. On the basis of Cl data, 35% of the injected water was recovered and 65% of the injected water and associated disinfection by-products (DBPs) remained in the aquifer at the end of extraction. About 46.3 kg of total trihalomethanes (TTHM) entered the aquifer with the injected water and 37.6 kg of TTHM were extracted. As much as 44 kg of TTHMs remained in the aquifer at the end of extraction because of incomplete recovery of injected water and formation of THMs within the aquifer by reactions with freechlorine in the injected water. Well-bore velocity log data collected from the Aquifer Storage Recovery (ASR) well show as much as 60% of the injected water entered the aquifer through a 9 m thick, high-permeability layer within the confined aquifer near the top of the screened interval. Model simulations of ground-water flow near the ASR well indicate that (1) aquifer heterogeneity allowed injected water to move rapidly through the aquifer to nearby monitoring wells, (2) aquifer heterogeneity caused injected water to move further than expected assuming uniform aquifer properties, and (3) physical clogging of high-permeability layers is the probable cause for the observed change in the distribution of borehole flow. Aquifer heterogeneity also enhanced mixing of native anoxic ground water with oxic injected water, promoting removal of THMs primarily through sorption. A 3 to 4-fold reduction in TTHM concentrations was observed in the furthest monitoring well 427 m downgradient from the ASR well, and similar magnitude reductions were observed in depth-dependent water samples collected from the upper part of the screened interval in the ASR well near the end of the extraction

State of the art and risk analysis for CO2 storage in a saline aquifer. Investigation report

International Nuclear Information System (INIS)

Farret, R.; Gombert, P.; Hulot, C.; BOUR, Olivier; Thoraval, Alain

2010-01-01

This study deals with the impact of supercritical CO 2 injection in deep saline aquifer, but also addresses the case of depleted hydrocarbons fields. After a general presentation of the carbon capture and storage (CCS) technique, this report presents the main principles of risk analysis and defines an analysis method applicable to the whole CCS sector. It is based on practices coming from the field of industrial risk analysis, on the knowledge of underground processes, and on the state of the art of health risk analysis in the case of chemical species. The main considered risks are hydraulic risks (fluid pressurization), mechanical risks (cracking, soil rising and induced seismicity), CO 2 migration or leakages towards aquifers and surface, and migration of other species than CO 2 . The report addresses the characterisation of fluids and of possible geochemical evolutions, the characterisation of scenarios of fluid migration, and the hierarchy of health impacts related to fluid leakages

Characterization of 200-UP-1 Aquifer Sediments and Results of Sorption-Desorption Tests Using Spiked Uncontaminated Groundwater

Energy Technology Data Exchange (ETDEWEB)

Um, Wooyong; Serne, R JEFFREY.; Bjornstad, Bruce N.; Schaef, Herbert T.; Brown, Christopher F.; Legore, Virginia L.; Geiszler, Keith N.; Baum, Steven R.; Valenta, Michelle M.; Kutnyakov, Igor V.; Vickerman, Tanya S.; Lindberg, Michael J.

2005-11-16

Core characterization showed only 4 out of 13 core liner samples were intact samples and that the others were slough material. The intact samples showed typical Ringold Unit E characteristics such as being dominated by gravel and sand. Moderately reducing conditions are inferred in some core from borehole C4299. This reducing condition was caused by the hard tool process used to drill the wells. One core showed significant presence of ferric iron oxide/clay coatings on the gravels. There were no highly contaminated sediments found in the cores from the three new boreholes in UP-1 operable unit, especially for uranium. The presence of slough and ''flour'' caused by hard tooling is a serious challenge to obtaining field relevant sediments for use in geochemical experiments to determine the adsorption-desorption tendencies of redox sensitive elements such as uranium. The adsorption of COCs on intact Ringold Formation sediments and Fe/clay coatings showed that most of the anionic contaminants [Tc(VII), Se(VI), U(VI), Cr(VI), and I(-I)] did not adsorbed very well compared to cationic [Np(V), Sr(II), and Cs(I)] radionuclides. The high hydrous iron oxide content in Fe/clay coatings caused the highest Kd values for U and Np, suggesting these hydrous oxides are the key solid adsorbent in the sediments. Enhanced adsorption behavior for Tc, and Cr and perhaps Se on the sediments was considered an ?artifact? result caused by the induced reducing conditions from the hard tool drilling. Additional U(VI) adsorption Kd studies were performed on Ringold Formation sediments to develop more robust Kd data base for U. The <2 mm size separates of three UP-1 sediments showed a linear U(VI) adsorption isotherm up 1 ppm of total U(VI) concentration in solution. The additional U(VI) Kds obtained from varying carbonate concentration indicated that U(VI) adsorption was strongly influenced by the concentration of carbonate in solution. U(VI) adsorption decreased with

Groundwater-quality data in the Monterey–Salinas shallow aquifer study unit, 2013: Results from the California GAMA Program

Science.gov (United States)

Goldrath, Dara A.; Kulongoski, Justin T.; Davis, Tracy A.

2016-09-01

constituents (trace elements, nutrients, major and minor ions, silica, total dissolved solids, and alkalinity) were collected at all 170 sites. In addition to these constituents, the samples from grid wells were analyzed for organic constituents (volatile organic compounds, pesticides and pesticide degradates), constituents of special interest (perchlorate and N-nitrosodimethylamine, or NDMA), radioactive constituents (radon-222 and gross-alpha and gross-beta radioactivity), and geochemical and age-dating tracers (stable isotopes of carbon in dissolved inorganic carbon, carbon-14 abundances, stable isotopes of hydrogen and oxygen in water, and tritium activities).Three types of quality-control samples (blanks, replicates, and matrix spikes) were collected at up to 11 percent of the wells in the Monterey–Salinas Shallow Aquifer study unit, and the results for these samples were used to evaluate the quality of the data from the groundwater samples. With the exception of trace elements, blanks rarely contained detectable concentrations of any constituent, indicating that contamination from sample-collection procedures was not a significant source of bias in the data for the groundwater samples. Low concentrations of some trace elements were detected in blanks; therefore, the data were re-censored at higher reporting levels. Replicate samples generally were within the limits of acceptable analytical reproducibility. The median values of matrix-spike recoveries were within the acceptable range (70 to 130 percent) for the volatile organic compounds (VOCs) and N-nitrosodimethylamine (NDMA), but were only approximately 64 percent for pesticides and pesticide degradates.The sample-collection protocols used in this study were designed to obtain representative samples of groundwater. The quality of groundwater can differ from the quality of drinking water because water chemistry can change as a result of contact with plumbing systems or the atmosphere; because of treatment

Quantification of anthropogenic impact on groundwater-dependent terrestrial ecosystem using geochemical and isotope tools combined with 3-D flow and transport modelling

Science.gov (United States)

Zurek, A. J.; Witczak, S.; Dulinski, M.; Wachniew, P.; Rozanski, K.; Kania, J.; Postawa, A.; Karczewski, J.; Moscicki, W. J.

2015-02-01

Groundwater-dependent ecosystems (GDEs) have important functions in all climatic zones as they contribute to biological and landscape diversity and provide important economic and social services. Steadily growing anthropogenic pressure on groundwater resources creates a conflict situation between nature and man which are competing for clean and safe sources of water. Such conflicts are particularly noticeable in GDEs located in densely populated regions. A dedicated study was launched in 2010 with the main aim to better understand the functioning of a groundwater-dependent terrestrial ecosystem (GDTE) located in southern Poland. The GDTE consists of a valuable forest stand (Niepolomice Forest) and associated wetland (Wielkie Błoto fen). It relies mostly on groundwater from the shallow Quaternary aquifer and possibly from the deeper Neogene (Bogucice Sands) aquifer. In July 2009 a cluster of new pumping wells abstracting water from the Neogene aquifer was set up 1 km to the northern border of the fen. A conceptual model of the Wielkie Błoto fen area for the natural, pre-exploitation state and for the envisaged future status resulting from intense abstraction of groundwater through the new well field was developed. The main aim of the reported study was to probe the validity of the conceptual model and to quantify the expected anthropogenic impact on the studied GDTE. A wide range of research tools was used. The results obtained through combined geologic, geophysical, geochemical, hydrometric and isotope investigations provide strong evidence for the existence of upward seepage of groundwater from the deeper Neogene aquifer to the shallow Quaternary aquifer supporting the studied GDTE. Simulations of the groundwater flow field in the study area with the aid of a 3-D flow and transport model developed for Bogucice Sands (Neogene) aquifer and calibrated using environmental tracer data and observations of hydraulic head in three different locations on the study area

Estimating Aquifer Properties Using Sinusoidal Pumping Tests

Science.gov (United States)

Rasmussen, T. C.; Haborak, K. G.; Young, M. H.

2001-12-01

We develop the theoretical and applied framework for using sinusoidal pumping tests to estimate aquifer properties for confined, leaky, and partially penetrating conditions. The framework 1) derives analytical solutions for three boundary conditions suitable for many practical applications, 2) validates the analytical solutions against a finite element model, 3) establishes a protocol for conducting sinusoidal pumping tests, and 4) estimates aquifer hydraulic parameters based on the analytical solutions. The analytical solutions to sinusoidal stimuli in radial coordinates are derived for boundary value problems that are analogous to the Theis (1935) confined aquifer solution, the Hantush and Jacob (1955) leaky aquifer solution, and the Hantush (1964) partially penetrated confined aquifer solution. The analytical solutions compare favorably to a finite-element solution of a simulated flow domain, except in the region immediately adjacent to the pumping well where the implicit assumption of zero borehole radius is violated. The procedure is demonstrated in one unconfined and two confined aquifer units near the General Separations Area at the Savannah River Site, a federal nuclear facility located in South Carolina. Aquifer hydraulic parameters estimated using this framework provide independent confirmation of parameters obtained from conventional aquifer tests. The sinusoidal approach also resulted in the elimination of investigation-derived wastes.

An evaluation of aquifer intercommunication between the unconfined and Rattlesnake Ridge aquifers on the Hanford Site

International Nuclear Information System (INIS)

Jensen, E.J.

1987-10-01

During 1986, Pacific Northwest Laboratory conducted a study of a portion of the Rattlesnake Ridge aquifer (confined aquifer) that lies beneath the B Pond - Gable Mountain Pond area of the Hanford Site. The purpose was to determine the extent of intercommunication between the unconfined aquifer and the uppermost regionally extensive confined aquifer, referred to as the Rattlesnake Ridge aquifer. Hydraulic head data and chemical data were collected from the ground water in the study area during December 1986. The hydraulic head data were used to determine the effects caused by water discharged to the ground from B Pond on both the water table of the unconfined aquifer and the potentiometric surface of the confined aquifer. The chemical data were collected to determine the extent of chemical constituents migrating from the unconfined aquifer to the confined aquifer. Analysis of chemical constituents in the Rattlesnake Ridge aquifer demonstrated that communication between the unconfined and confined aquifers had occurred. However, the levels of contaminants found in the Rattlesnake Ridge aquifer during this study were below the DOE Derived Concentration Guides

Surface complexation modeling of groundwater arsenic mobility: Results of a forced gradient experiment in a Red River flood plain aquifer, Vietnam

DEFF Research Database (Denmark)

Jessen, Søren; Postma, Dieke; Larsen, Flemming

2012-01-01

, suggesting a comparable As(III) affinity of Holocene and Pleistocene aquifer sediments. A forced gradient field experiment was conducted in a bank aquifer adjacent to a tributary channel to the Red River, and the passage in the aquifer of mixed groundwater containing up to 74% channel water was observed......Three surface complexation models (SCMs) developed for, respectively, ferrihydrite, goethite and sorption data for a Pleistocene oxidized aquifer sediment from Bangladesh were used to explore the effect of multicomponent adsorption processes on As mobility in a reduced Holocene floodplain aquifer......(III) while PO43− and Fe(II) form the predominant surface species. The SCM for Pleistocene aquifer sediment resembles most the goethite SCM but shows more Si sorption. Compiled As(III) adsorption data for Holocene sediment was also well described by the SCM determined for Pleistocene aquifer sediment...

Recharge sources and residence times of groundwater as determined by geochemical tracers in the Mayfield Area, southwestern Idaho, 2011–12

Science.gov (United States)

Hopkins, Candice B.

2013-01-01

Parties proposing residential development in the area of Mayfield, Idaho are seeking a sustainable groundwater supply. During 2011–12, the U.S. Geological Survey, in cooperation with the Idaho Department of Water Resources, used geochemical tracers in the Mayfield area to evaluate sources of aquifer recharge and differences in groundwater residence time. Fourteen groundwater wells and one surface-water site were sampled for major ion chemistry, metals, stable isotopes, and age tracers; data collected from this study were used to evaluate the sources of groundwater recharge and groundwater residence times in the area. Major ion chemistry varied along a flow path between deeper wells, suggesting an upgradient source of dilute water, and a downgradient source of more concentrated water with the geochemical signature of the Idaho Batholith. Samples from shallow wells had elevated nutrient concentrations, a more positive oxygen-18 signature, and younger carbon-14 dates than deep wells, suggesting that recharge comes from young precipitation and surface-water infiltration. Samples from deep wells generally had higher concentrations of metals typical of geothermal waters, a more negative oxygen-18 signature, and older carbon-14 values than samples from shallow wells, suggesting that recharge comes from both infiltration of meteoric water and another source. The chemistry of groundwater sampled from deep wells is somewhat similar to the chemistry in geothermal waters, suggesting that geothermal water may be a source of recharge to this aquifer. Results of NETPATH mixing models suggest that geothermal water composes 1–23 percent of water in deep wells. Chlorofluorocarbons were detected in every sample, which indicates that all groundwater samples contain at least a component of young recharge, and that groundwater is derived from multiple recharge sources. Conclusions from this study can be used to further refine conceptual hydrological models of the area.

Aquifer test results, 200-UP-1 operable unit IRM plume: Wells 299-W19-39 and 299-W19-36

International Nuclear Information System (INIS)

Swanson, L.C.

1996-03-01

An aquifer test was conducted at 200-UP-1 extraction well 299-W19-39 from September 6 to 8, 1995. The testing process consisted of pumping groundwater from the extraction well, using the surface treatment system to purify the water, and reinjecting the water through well 299-W19-36. Multiple observation wells were used to measure the response of the aquifer during the pumping and recovery phases of the test. Tables 1 and 2 list each well monitored and give well location and configuration information. Pretest monitoring initiated on August 31, 1995 was used to establish water-level trends and barometric pressure responses in the extraction, injection, and observation wells. Water-level monitoring continued for about 2 weeks after pumping ceased. The objectives of the aquifer test were to determine large-scale aquifer properties to confirm hydraulic conductivity input values used in previous numerical modeling work, to evaluate the long-term performance of the extraction and monitoring wells, and to estimate the radial extent of the drawdown cone (i.e., the expected capture area and depth). All of the test objectives were met. A discussion of the test results follows

Surface complexation modeling for predicting solid phase arsenic concentrations in the sediments of the Mississippi River Valley alluvial aquifer, Arkansas, USA

Science.gov (United States)

Sharif, M.S.U.; Davis, R.K.; Steele, K.F.; Kim, B.; Hays, P.D.; Kresse, T.M.; Fazio, J.A.

2011-01-01

The potential health impact of As in drinking water supply systems in the Mississippi River Valley alluvial aquifer in the state of Arkansas, USA is significant. In this context it is important to understand the occurrence, distribution and mobilization of As in the Mississippi River Valley alluvial aquifer. Application of surface complexation models (SCMs) to predict the sorption behavior of As and hydrous Fe oxides (HFO) in the laboratory has increased in the last decade. However, the application of SCMs to predict the sorption of As in natural sediments has not often been reported, and such applications are greatly constrained by the lack of site-specific model parameters. Attempts have been made to use SCMs considering a component additivity (CA) approach which accounts for relative abundances of pure phases in natural sediments, followed by the addition of SCM parameters individually for each phase. Although few reliable and internally consistent sorption databases related to HFO exist, the use of SCMs using laboratory-derived sorption databases to predict the mobility of As in natural sediments has increased. This study is an attempt to evaluate the ability of the SCMs using the geochemical code PHREEQC to predict solid phase As in the sediments of the Mississippi River Valley alluvial aquifer in Arkansas. The SCM option of the double-layer model (DLM) was simulated using ferrihydrite and goethite as sorbents quantified from chemical extractions, calculated surface-site densities, published surface properties, and published laboratory-derived sorption constants for the sorbents. The model results are satisfactory for shallow wells (10.6. m below ground surface), where the redox condition is relatively oxic or mildly suboxic. However, for the deep alluvial aquifer (21-36.6. m below ground surface) where the redox condition is suboxic to anoxic, the model results are unsatisfactory. ?? 2011 Elsevier Ltd.

Geochemical modeling: a review

International Nuclear Information System (INIS)

Jenne, E.A.

1981-06-01

Two general families of geochemical models presently exist. The ion speciation-solubility group of geochemical models contain submodels to first calculate a distribution of aqueous species and to secondly test the hypothesis that the water is near equilibrium with particular solid phases. These models may or may not calculate the adsorption of dissolved constituents and simulate the dissolution and precipitation (mass transfer) of solid phases. Another family of geochemical models, the reaction path models, simulates the stepwise precipitation of solid phases as a result of reacting specified amounts of water and rock. Reaction path models first perform an aqueous speciation of the dissolved constituents of the water, test solubility hypotheses, then perform the reaction path modeling. Certain improvements in the present versions of these models would enhance their value and usefulness to applications in nuclear-waste isolation, etc. Mass-transfer calculations of limited extent are certainly within the capabilities of state-of-the-art models. However, the reaction path models require an expansion of their thermodynamic data bases and systematic validation before they are generally accepted

Geochemical modeling: a review

Energy Technology Data Exchange (ETDEWEB)

Jenne, E.A.

1981-06-01

Two general families of geochemical models presently exist. The ion speciation-solubility group of geochemical models contain submodels to first calculate a distribution of aqueous species and to secondly test the hypothesis that the water is near equilibrium with particular solid phases. These models may or may not calculate the adsorption of dissolved constituents and simulate the dissolution and precipitation (mass transfer) of solid phases. Another family of geochemical models, the reaction path models, simulates the stepwise precipitation of solid phases as a result of reacting specified amounts of water and rock. Reaction path models first perform an aqueous speciation of the dissolved constituents of the water, test solubility hypotheses, then perform the reaction path modeling. Certain improvements in the present versions of these models would enhance their value and usefulness to applications in nuclear-waste isolation, etc. Mass-transfer calculations of limited extent are certainly within the capabilities of state-of-the-art models. However, the reaction path models require an expansion of their thermodynamic data bases and systematic validation before they are generally accepted.

Metal and acidity fluxes controlled by precipitation/dissolution cycles of sulfate salts in an anthropogenic mine aquifer.

Science.gov (United States)

Cánovas, C R; Macías, F; Pérez-López, R

2016-05-01

Underground mine drainages are extremely difficult to study due to the lack of information about the flow path and source proximity in relation to the outflow adit. Geochemical processes controlling metals and acidity fluxes in a complex anthropogenic mine aquifer in SW Spain during the dry and rainy season were investigated by geochemical and statistical tools. High concentrations of acidity, sulfate, metals and metalloids (e.g. Fe, Cu, Zn, As, Cd, Ni, Co) were observed due to intense sulfide oxidation processes. The high residence time inside the anthropogenic aquifer, around 40days, caused the release of significant quantities of metals linked to host rocks (e.g. Al, Ca, Ge, Li, Mg, REE). The most outstanding characteristic of the acid mine drainage (AMD) outflows is the existence of higher Fe/SO4 molar ratios than those theoretical of pyrite (0.50) during most of the monitored period, due to a fire which occurred in 1949 and remained active for decades. Permanent and temporal retention mechanisms of acidity and metals were observed in the galleries. Once released from sulfide oxidation, Pb and As are sorbed on Fe oxyhydroxysulfate or precipitated as low solubility minerals (i.e. anglesite) inside the galleries. The precipitation of evaporitic sulfate salts during the dry season and the subsequent re-dissolution after rainfall control the fluxes of acidity and main metals (i.e. Fe, Mg, Al) from this anthropogenic aquifer. Some elements, such as Cd, Cu, Ni, REE and Zn, are retained in highly soluble sulfate salts while other elements, such as Ge, Pb and Sc, have a lower response to washout processes due to its incorporation in less soluble sulfate salts. In this way, metal concentration during the washout processes would be controlled by the proportion and solubility of each type of evaporitic sulfate salt stored during the dry season. The recovery of metals of economic interest contained in the AMD could help to self-finance the remediation of these waters in

Diagnosis of the Ghiss Nekor aquifer in order to elaborate the aquifer contract

Science.gov (United States)

Baite, Wissal; Boukdir, A.; Zitouni, A.; Dahbi, S. D.; Mesmoudi, H.; Elissami, A.; Sabri, E.; Ikhmerdi, H.

2018-05-01

The Ghiss-Nekor aquifer, located in the north-east of the action area of the ABHL, plays a strategic role in the drinkable water supply of the city of Al Hoceima and of the neighboring urban areas. It also participates in the irrigation of PMH. However, this aquifer has problems such as over-exploitation and pollution. In the face of these problems, the only Solution is the establishment of a new mode of governance, which privileges the participation, the involvement and the responsibility of the actors concerned in a negotiated contractual framework, namely the aquifer contract. The purpose of this study is to diagnose the current state of the Ghiss Nekor aquifer, the hydrogeological characterization of the aquifer, the use of the waters of the aquifer, the Problem identification and the introduction of the aquifer contract, which aims at the participatory and sustainable management of underground water resources in the Ghiss- Nekor plain, to ensure sustainable development.

Geochemical mole-balance modeling with uncertain data

Science.gov (United States)

Parkhurst, David L.

1997-01-01

Geochemical mole-balance models are sets of chemical reactions that quantitatively account for changes in the chemical and isotopic composition of water along a flow path. A revised mole-balance formulation that includes an uncertainty term for each chemical and isotopic datum is derived. The revised formulation is comprised of mole-balance equations for each element or element redox state, alkalinity, electrons, solvent water, and each isotope; a charge-balance equation and an equation that relates the uncertainty terms for pH, alkalinity, and total dissolved inorganic carbon for each aqueous solution; inequality constraints on the size of the uncertainty terms; and inequality constraints on the sign of the mole transfer of reactants. The equations and inequality constraints are solved by a modification of the simplex algorithm combined with an exhaustive search for unique combinations of aqueous solutions and reactants for which the equations and inequality constraints can be solved and the uncertainty terms minimized. Additional algorithms find only the simplest mole-balance models and determine the ranges of mixing fractions for each solution and mole transfers for each reactant that are consistent with specified limits on the uncertainty terms. The revised formulation produces simpler and more robust mole-balance models and allows the significance of mixing fractions and mole transfers to be evaluated. In an example from the central Oklahoma aquifer, inclusion of up to 5% uncertainty in the chemical data can reduce the number of reactants in mole-balance models from seven or more to as few as three, these being cation exchange, dolomite dissolution, and silica precipitation. In another example from the Madison aquifer, inclusion of the charge-balance constraint requires significant increases in the mole transfers of calcite, dolomite, and organic matter, which reduce the estimated maximum carbon 14 age of the sample by about 10,000 years, from 22,700 years to

Reactive Transport of Marcellus Shale Waters in Natural Aquifers: the Role of Mineralogical Compositions and Spatial Distribution Patterns

Science.gov (United States)

Cai, Z.; Wen, H.; Li, L.

2017-12-01

Accidental release of Marcellus Shale waters (MSW) can release high concentrations of chemicals that can deteriorate groundwater quality. It is important to understand the reactive transport and fate of chemicals from MSW. Natural aquifers typically have complex mineralogical compositions and are heterogeneous with large spatial variation in terms of physical and geochemical properties. To investigate the effects of mineralogical compositions, flow-through experiments and reactive transport modeling were carried out using 3 large columns (5 cm×50 cm, Quartz, Calcite, and Vermiculite). Results indicate calcite immobilizes heavy metals by precipitation and solid solution partitioning (coprecipitation). Vermiculite retards heavy metals through ion exchange. The sorbed chemicals however slowly release back to the groundwater. Na and Ca transport similarly to Br in Qtz and Cal columns however become sorbed in Vrm column during release through ion exchange by 27.8% and 46.5%, respectively and later slowly release back to aqueous phase. To understand the role of mineral spatial patterns, three 2D flow-cell (40 cm×12 cm×1 cm) experiments were carried out. All flow cells have the same clay mass within quartz matrix but different spatial patterns characterized by the relative length of the clay zone ( 0, ¼, ½) of the domain length (L). Results show that in the uniform column, ion exchange dominates and most Ba sorbs to the solid phase, to an extent Ba cannot precipitate out with SO4 as barite. In 1/2-Zone, however, most Ba precipitates as barite. In 1/4-Zone, both ion exchange and mineral precipitation occur. In general, the 1/2-Zone has the smallest ion exchange capacity for other species including Na, Ca, Mg, K and heavy metals (Mn, Cu, Zn, Cd and Pb) as well. Our flow cell experiment emphasizes the importance of mineral spatial patterns in regulating not only reaction rates but also the type of reactions in controlling the reactive transport of MSW chemicals. The

PHAST--a program for simulating ground-water flow, solute transport, and multicomponent geochemical reactions

Science.gov (United States)

Parkhurst, David L.; Kipp, Kenneth L.; Engesgaard, Peter; Charlton, Scott R.

2004-01-01

The computer program PHAST simulates multi-component, reactive solute transport in three-dimensional saturated ground-water flow systems. PHAST is a versatile ground-water flow and solute-transport simulator with capabilities to model a wide range of equilibrium and kinetic geochemical reactions. The flow and transport calculations are based on a modified version of HST3D that is restricted to constant fluid density and constant temperature. The geochemical reactions are simulated with the geochemical model PHREEQC, which is embedded in PHAST. PHAST is applicable to the study of natural and contaminated ground-water systems at a variety of scales ranging from laboratory experiments to local and regional field scales. PHAST can be used in studies of migration of nutrients, inorganic and organic contaminants, and radionuclides; in projects such as aquifer storage and recovery or engineered remediation; and in investigations of the natural rock-water interactions in aquifers. PHAST is not appropriate for unsaturated-zone flow, multiphase flow, density-dependent flow, or waters with high ionic strengths. A variety of boundary conditions are available in PHAST to simulate flow and transport, including specified-head, flux, and leaky conditions, as well as the special cases of rivers and wells. Chemical reactions in PHAST include (1) homogeneous equilibria using an ion-association thermodynamic model; (2) heterogeneous equilibria between the aqueous solution and minerals, gases, surface complexation sites, ion exchange sites, and solid solutions; and (3) kinetic reactions with rates that are a function of solution composition. The aqueous model (elements, chemical reactions, and equilibrium constants), minerals, gases, exchangers, surfaces, and rate expressions may be defined or modified by the user. A number of options are available to save results of simulations to output files. The data may be saved in three formats: a format suitable for viewing with a text editor; a

Concerning evaluation of eco-geochemical background in remediation strategy

Science.gov (United States)

Korobova, Elena; Romanov, Sergey

2015-04-01

The geochemical concept of biosphere developed by V.I. Vernadsky states the geological role of the living organisms in the course of their active chemical interaction with the inert matter (Vernadsky, 1926, 1960). Basing on this theory it is reasonable to suggest that coevolution of living organisms and their environment led to development of the dynamically stable biogeocenoses precisely adequate to their geochemical environment. Soil cover was treated by V.I. Vernadsky as a balanced bio-inert matter resulting from this interaction. Appearance of human mind and then a civilization led to global expansion of human beings, first able to survive in unfavorable geochemical conditions and then starting chemical transformation of the environment to satisfy the growing demands of mankind in food and energy. The residence in unfavorable environment and local contamination was followed by appearance of endemic diseases of plants, animals and man. Therefore zonal, regional and local chemical composition of the soil cover formed in natural conditions may be used for estimation of the optimum geochemical background, most adequate for the corresponding zonal biogeocenoses and species. Moreover, the natural geochemical background and technogenic fields have unequal spatial structure and this facilitates their identification that may be relatively easy realized in remediation strategy. On the assumption of the foregoing, the adequate methodical approach to remediation of technogenically affected areas should account of the interaction of the existing natural and the newly formed technogenic geochemical fields and include the following steps: 1) the study and mapping of geochemical structure of the natural geochemical background basing on soil maps; 2) the study of contaminants and mapping spatial distribution of technogenic releases; 3) construction of risk maps for the target risk groups with due regard to natural ecological threshold concentration in context of risk degree for

EPA Region 1 Sole Source Aquifers

Science.gov (United States)

This coverage contains boundaries of EPA-approved sole source aquifers. Sole source aquifers are defined as an aquifer designated as the sole or principal source of drinking water for a given aquifer service area; that is, an aquifer which is needed to supply 50% or more of the drinking water for the area and for which there are no reasonable alternative sources should the aquifer become contaminated.The aquifers were defined by a EPA hydrogeologist. Aquifer boundaries were then drafted by EPA onto 1:24000 USGS quadrangles. For the coastal sole source aquifers the shoreline as it appeared on the quadrangle was used as a boundary. Delineated boundaries were then digitized into ARC/INFO.

Origins and delineation of saltwater intrusion in the Biscayne aquifer and changes in the distribution of saltwater in Miami-Dade County, Florida

Science.gov (United States)

Prinos, Scott T.; Wacker, Michael A.; Cunningham, Kevin J.; Fitterman, David V.

2014-01-01

Intrusion of saltwater into parts of the shallow karst Biscayne aquifer is a major concern for the 2.5 million residents of Miami-Dade County that rely on this aquifer as their primary drinking water supply. Saltwater intrusion of this aquifer began when the Everglades were drained to provide dry land for urban development and agriculture. The reduction in water levels caused by this drainage, combined with periodic droughts, allowed saltwater to flow inland along the base of the aquifer and to seep directly into the aquifer from the canals. The approximate inland extent of saltwater was last mapped in 1995. An examination of the inland extent of saltwater and the sources of saltwater in the aquifer was completed during 2008–2011 by using (1) all available salinity information, (2) time-series electromagnetic induction log datasets from 35 wells, (3) time-domain electromagnetic soundings collected at 79 locations, (4) a helicopter electromagnetic survey done during 2001 that was processed, calibrated, and published during the study, (5) cores and geophysical logs collected from 8 sites for stratigraphic analysis, (6) 8 new water-quality monitoring wells, and (7) analyses of 69 geochemical samples. The results of the study indicate that as of 2011 approximately 1,200 square kilometers (km2) of the mainland part of the Biscayne aquifer were intruded by saltwater. The saltwater front was mapped farther inland than it was in 1995 in eight areas totaling about 24.1 km2. In many of these areas, analyses indicated that saltwater had encroached along the base of the aquifer. The saltwater front was mapped closer to the coast than it was in 1995 in four areas totaling approximately 6.2 km2. The changes in the mapped extent of saltwater resulted from improved spatial information, actual movement of the saltwater front, or a combination of both. Salinity monitoring in some of the canals in Miami-Dade County between 1988 and 2010 indicated influxes of saltwater, with maximum

Evidence for Upward Flow of Saline Water from Depth into the Mississippi River Valley Alluvial Aquifer in Southeastern Arkansas

Science.gov (United States)

Larsen, D.; Paul, J.

2017-12-01

Groundwater salinization is occurring in the Mississippi River Valley Alluvial (MRVA) aquifer in southeastern Arkansas (SE AR). Water samples from the MRVA aquifer in Chicot and Desha counties have yielded elevated Cl-concentrations with some as high as 1,639 mg/L. Considering that the MRVA aquifer is the principle source of irrigation water for the agricultural economy of SE AR, salinization needs to be addressed to ensure the sustainability of crop, groundwater, and soil resources in the area. The origin of elevated salinity in MRVA aquifer was investigated using spatial and factor analysis of historical water quality data, and sampling and tracer analysis of groundwater from irrigation, municipal, and flowing industrial wells in SE AR. Spatial analysis of Cl- data in relation to soil type, geomorphic features and sand-blow density indicate that the Cl- anomalies are more closely related to the sand-blow density than soil data, suggesting an underlying tectonic control for the distribution of salinity. Factor analysis of historical geochemical data from the MRVA and underlying Sparta aquifer shows dilute and saline groups, with saline groups weighted positively with Cl- or Na+ and Cl-. Tracer data suggest a component of evaporatively evolved crustal water of pre-modern age has mixed with younger, fresher meteoric sources in SE AR to create the saline conditions in the MRVA aquifer. Stable hydrogen and oxygen values of waters sampled from the Tertiary Sparta and MRVA aquifers deviate from the global and local meteoric water lines along an evaporative trend (slope=4.4) and mixing line with Eocene Wilcox Group groundwaters. Ca2+ and Cl- contents vary with Br- along mixing trends between dilute MRVA water and Jurassic Smackover Formation pore fluids in southern AR. Increasing Cl- content with C-14 age in MRVA aquifer groundwater suggests that the older waters are more saline. Helium isotope ratios decrease with He gas content for more saline water, consistent with

Engineered in situ bioremediation of a petroleum hydrocarbon-contaminated aquifer: assessment of mineralization based on alkalinity, inorganic carbon and stable carbon isotope balances

Science.gov (United States)

Hunkeler, Daniel; Höhener, Patrick; Bernasconi, Stefano; Zeyer, Josef

1999-04-01

A concept is proposed to assess in situ petroleum hydrocarbon mineralization by combining data on oxidant consumption, production of reduced species, CH 4, alkalinity and dissolved inorganic carbon (DIC) with measurements of stable isotope ratios. The concept was applied to a diesel fuel contaminated aquifer in Menziken, Switzerland, which was treated by engineered in situ bioremediation. In the contaminated aquifer, added oxidants (O 2 and NO 3-) were consumed, elevated concentrations of Fe(II), Mn(II), CH 4, alkalinity and DIC were detected and the DIC was generally depleted in 13C compared to the background. The DIC production was larger than expected based on the consumption of dissolved oxidants and the production of reduced species. Stable carbon isotope balances revealed that the DIC production in the aquifer originated mainly from microbial petroleum hydrocarbon mineralization, and that geochemical reactions such as carbonate dissolution produced little DIC. This suggests that petroleum hydrocarbon mineralization can be underestimated if it is determined based on concentrations of dissolved oxidants and reduced species.

The limited role of aquifer heterogeneity on metal reduction in an Atlantic coastal plain determined by push-pull tests

International Nuclear Information System (INIS)

Mailloux, Brian J.; Devlin, Stephanie; Fuller, Mark E.; Onstott, T.C.; De Flaun, Mary F.; Choi, K.-H.; Green-Blum, Maria; Swift, Donald J.P.; McCarthy, John; Dong Hailiang

2007-01-01

Sixty push-pull experiments were conducted to determine the factors controlling Fe(III) and Mn(IV) reduction in a well-characterized, shallow, coastal plain aquifer near Oyster, VA, USA. The five multi-level samplers each equipped with 12 ports sampled a heterogeneous portion of the aquifer from 4.4 to 8m-bgs. Each multi-level sampler (MLS) was injected with groundwater that contained NO 3 - and Br - along with: (1) just groundwater (control treatment), (2) humics, (3) lactate (conducted twice) and (4) lactate plus humics. Microbially mediated Fe(III) reduction caused the aqueous Fe Tot concentrations to increase at every depth in the lactate treatment with significant increases within 1 day even while NO 3 - was present. Little change in the Fe Tot concentrations were observed in the control and humics treatment. Humics may have acted as an electron shuttle to increase Fe(III) reduction in the lactate plus humics treatment. The amount of Mn(IV) reduction was significantly lower than that of Fe(III) reduction. Geochemical modeling indicated that gas formation, sorption on reactive surfaces, and mineral precipitation were important processes and that Fe(III) and SO 4 2- reduction were co-occurring. Conditions were favorable for the precipitation of Fe-carbonates, Fe-sulfides and Fe-silicates. In the lactate treatment protist concentrations increased then decreased and planktonic cell concentrations steadily increased, whereas no change was observed in the control treatment. Correlations of Fe(III) reduction with physical and chemical heterogeneity were weak, probably as a result of the abundance of Fe(III) bearing minerals relative to electron donor abundance and that the push-pull test sampled a representative elemental volume that encompassed the microbial diversity within the aquifer. This work indicates that stimulating metal reduction in aquifer systems is a feasible method for remediating heterogeneous subsurface sites contaminated with metals and

Groundwater evolution in the Continental Intercalaire aquifer of southern Algeria and Tunisia: trace element and isotopic indicators

International Nuclear Information System (INIS)

Edmunds, W.M.; Guendouz, A.H.; Mamou, A.; Moulla, A.; Shand, P.; Zouari, K.

2003-01-01

The geochemical processes taking place along an 800 km flow line in the non-carbonate Continental Intercalaire aquifer (CI) aquifer in North Africa are described using chemical (major and trace element) and isotopic indicators. The aquifer is hydraulically continuous from the Atlas Mountains in Algeria to the Chotts of Tunisia and the geochemical evidence corroborates this. The highest discharge temperature is 73 deg. C but silica geothermometry indicates a maximum temperature of 94 deg. C at depth. Chloride concentrations increase from 200 to 800 mg l -1 and the Br/Cl ratios confirm the dissolution of non-marine evaporites or interstitial waters as the main source of salinity. Fluoride concentrations are low and are likely to be derived from rainfall, recording oscillations in source. Radiocarbon ages, except near outcrop, are at or near detection limits and the δ 18 O and δ 2 H values indicate a cooler recharge regime with rainfall having lower primary evaporation than today. This is shown by the fact that mean isotope ratios of CI waters are around 3 per mille lighter than the present-day weighted mean value for rain. Major ion ratios and most trace elements indicate that despite the complex structure and stratigraphy, uniform evolution with continuous water-rock interaction takes place along the flow lines, which are only disturbed near the Tunisian Chotts by groundwater converging from additional flow lines. The ageing of the water can also be followed by the smooth increase in several indicator elements such as Li, K and Mn which are least affected by solubility controls. Similarly the influence of marine facies in the Tunisian sector may be recognised by the changing Mg/Ca and higher Br/Cl as well as trace element indicators. The groundwaters are oxidising up to 300 km from outcrop (dissolved O 2 has persisted for at least 20 ka) and within this zone the concentrations of several elements forming oxy-anions, such as U and Cr, increase and NO 3 remains

Occurrence and origin of methane in groundwater in Alberta (Canada): Gas geochemical and isotopic approaches

International Nuclear Information System (INIS)

Humez, P.; Mayer, B.; Ing, J.; Nightingale, M.; Becker, V.; Kingston, A.; Akbilgic, O.; Taylor, S.

2016-01-01

To assess potential future impacts on shallow aquifers by leakage of natural gas from unconventional energy resource development it is essential to establish a reliable baseline. Occurrence of methane in shallow groundwater in Alberta between 2006 and 2014 was assessed and was ubiquitous in 186 sampled monitoring wells. Free and dissolved gas sampling and measurement approaches yielded comparable results with low methane concentrations in shallow groundwater, but in 28 samples from 21 wells methane exceeded 10 mg/L in dissolved gas and 300,000 ppmv in free gas. Methane concentrations in free and dissolved gas samples were found to increase with well depth and were especially elevated in groundwater obtained from aquifers containing coal seams and shale units. Carbon isotope ratios of methane averaged − 69.7 ± 11.1‰ (n = 63) in free gas and − 65.6 ± 8.9‰ (n = 26) in dissolved gas. δ"1"3C values were not found to vary with well depth or lithology indicating that methane in Alberta groundwater was derived from a similar source. The low δ"1"3C values in concert with average δ"2H_C_H_4 values of − 289 ± 44‰ (n = 45) suggest that most methane was of biogenic origin predominantly generated via CO_2 reduction. This interpretation is confirmed by dryness parameters typically > 500 due to only small amounts of ethane and a lack of propane in most samples. Comparison with mud gas profile carbon isotope data revealed that methane in the investigated shallow groundwater in Alberta is isotopically similar to hydrocarbon gases found in 100–250 meter depths in the WCSB and is currently not sourced from thermogenic hydrocarbon occurrences in deeper portions of the basin. The chemical and isotopic data for methane gas samples obtained from Alberta groundwater provide an excellent baseline against which potential future impact of deeper stray gases on shallow aquifers can be assessed. - Highlights: • Analysis of gas geochemical data from 186 monitoring wells in

Occurrence and origin of methane in groundwater in Alberta (Canada): Gas geochemical and isotopic approaches

Energy Technology Data Exchange (ETDEWEB)

Humez, P., E-mail: phumez@ucalgary.ca [Department of Geoscience, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4 (Canada); Mayer, B.; Ing, J.; Nightingale, M.; Becker, V.; Kingston, A. [Department of Geoscience, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4 (Canada); Akbilgic, O. [Department of Geoscience, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4 (Canada); UTHSC-ORNL Center for Biomedical Informatics, 910 Madison Avenue, Memphis, TN, 38104 (United States); Taylor, S. [Department of Geoscience, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4 (Canada)

2016-01-15

To assess potential future impacts on shallow aquifers by leakage of natural gas from unconventional energy resource development it is essential to establish a reliable baseline. Occurrence of methane in shallow groundwater in Alberta between 2006 and 2014 was assessed and was ubiquitous in 186 sampled monitoring wells. Free and dissolved gas sampling and measurement approaches yielded comparable results with low methane concentrations in shallow groundwater, but in 28 samples from 21 wells methane exceeded 10 mg/L in dissolved gas and 300,000 ppmv in free gas. Methane concentrations in free and dissolved gas samples were found to increase with well depth and were especially elevated in groundwater obtained from aquifers containing coal seams and shale units. Carbon isotope ratios of methane averaged − 69.7 ± 11.1‰ (n = 63) in free gas and − 65.6 ± 8.9‰ (n = 26) in dissolved gas. δ{sup 13}C values were not found to vary with well depth or lithology indicating that methane in Alberta groundwater was derived from a similar source. The low δ{sup 13}C values in concert with average δ{sup 2}H{sub CH4} values of − 289 ± 44‰ (n = 45) suggest that most methane was of biogenic origin predominantly generated via CO{sub 2} reduction. This interpretation is confirmed by dryness parameters typically > 500 due to only small amounts of ethane and a lack of propane in most samples. Comparison with mud gas profile carbon isotope data revealed that methane in the investigated shallow groundwater in Alberta is isotopically similar to hydrocarbon gases found in 100–250 meter depths in the WCSB and is currently not sourced from thermogenic hydrocarbon occurrences in deeper portions of the basin. The chemical and isotopic data for methane gas samples obtained from Alberta groundwater provide an excellent baseline against which potential future impact of deeper stray gases on shallow aquifers can be assessed. - Highlights: • Analysis of gas geochemical data from 186

TAPIR--Finnish national geochemical baseline database.

Science.gov (United States)

Jarva, Jaana; Tarvainen, Timo; Reinikainen, Jussi; Eklund, Mikael

2010-09-15

In Finland, a Government Decree on the Assessment of Soil Contamination and Remediation Needs has generated a need for reliable and readily accessible data on geochemical baseline concentrations in Finnish soils. According to the Decree, baseline concentrations, referring both to the natural geological background concentrations and the diffuse anthropogenic input of substances, shall be taken into account in the soil contamination assessment process. This baseline information is provided in a national geochemical baseline database, TAPIR, that is publicly available via the Internet. Geochemical provinces with elevated baseline concentrations were delineated to provide regional geochemical baseline values. The nationwide geochemical datasets were used to divide Finland into geochemical provinces. Several metals (Co, Cr, Cu, Ni, V, and Zn) showed anomalous concentrations in seven regions that were defined as metal provinces. Arsenic did not follow a similar distribution to any other elements, and four arsenic provinces were separately determined. Nationwide geochemical datasets were not available for some other important elements such as Cd and Pb. Although these elements are included in the TAPIR system, their distribution does not necessarily follow the ones pre-defined for metal and arsenic provinces. Regional geochemical baseline values, presented as upper limit of geochemical variation within the region, can be used as trigger values to assess potential soil contamination. Baseline values have also been used to determine upper and lower guideline values that must be taken into account as a tool in basic risk assessment. If regional geochemical baseline values are available, the national guideline values prescribed in the Decree based on ecological risks can be modified accordingly. The national geochemical baseline database provides scientifically sound, easily accessible and generally accepted information on the baseline values, and it can be used in various

A novel analytical solution for estimating aquifer properties within a horizontally anisotropic aquifer bounded by a stream

Science.gov (United States)

Huang, Yibin; Zhan, Hongbin; Knappett, Peter S. K.

2018-04-01

Past studies modeling stream-aquifer interaction commonly account for vertical anisotropy in hydraulic conductivity, but rarely address horizontal anisotropy, which may exist in certain sedimentary environments. If present, horizontal anisotropy will greatly impact stream depletion and the amount of recharge a pumped aquifer captures from the river. This scenario requires a different and somewhat more sophisticated mathematical approach to model and interpret pumping test results than previous models used to describe captured recharge from rivers. In this study, a new mathematical model is developed to describe the spatiotemporal distribution of drawdown from stream-bank pumping with a well screened across a horizontally anisotropic, confined aquifer, laterally bounded by a river. This new model is used to estimate four aquifer parameters including the magnitude and directions of major and minor principal transmissivities and storativity based on the observed drawdown-time curves within a minimum of three non-collinear observation wells. In order to approve the efficacy of the new model, a MATLAB script file is programmed to conduct a four-parameter inversion to estimate the four parameters of concern. By comparing the results of analytical and numerical inversions, the accuracy of estimated results from both inversions is acceptable, but the MATLAB program sometimes becomes problematic because of the difficulty of separating the local minima from the global minima. It appears that the new analytical model of this study is applicable and robust in estimating parameter values for a horizontally anisotropic aquifer laterally bounded by a stream. Besides that, the new model calculates stream depletion rate as a function of stream-bank pumping. Unique to horizontally anisotropic and homogeneous aquifers, the stream depletion rate at any given pumping rate depends closely on the horizontal anisotropy ratio and the direction of the principle transmissivities relative to

Estimating Groundwater Mounding in Sloping Aquifers for Managed Aquifer Recharge.

Science.gov (United States)

Zlotnik, Vitaly A; Kacimov, Anvar; Al-Maktoumi, Ali

2017-11-01

Design of managed aquifer recharge (MAR) for augmentation of groundwater resources often lacks detailed data, and simple diagnostic tools for evaluation of the water table in a broad range of parameters are needed. In many large-scale MAR projects, the effect of a regional aquifer base dip cannot be ignored due to the scale of recharge sources (e.g., wadis, streams, reservoirs). However, Hantush's (1967) solution for a horizontal aquifer base is commonly used. To address sloping aquifers, a new closed-form analytical solution for water table mound accounts for the geometry and orientation of recharge sources at the land surface with respect to the aquifer base dip. The solution, based on the Dupiuit-Forchheimer approximation, Green's function method, and coordinate transformations is convenient for computing. This solution reveals important MAR traits in variance with Hantush's solution: mounding is limited in time and space; elevation of the mound is strongly affected by the dip angle; and the peak of the mound moves over time. These findings have important practical implications for assessment of various MAR scenarios, including waterlogging potential and determining proper rates of recharge. Computations are illustrated for several characteristic MAR settings. © 2017, National Ground Water Association.

Assessment of the groundwater chemistry of a complex aquifer system in the context of urbanization in Sub-Saharan Africa: case study in semiarid southwest Niger

Science.gov (United States)

Boubakar Hassane, A.; Favreau, G.; Leduc, C.; Ousmane, B.; Soumaila, A.

2010-12-01

The groundwater chemistry in the local vicinity of the city of Niamey was investigated in order to identify the origin of the groundwater mineralization and, in particular, to elucidate the impact of urbanization on the groundwater resources. Sources of pollution of concern in the urban area are solid waste and material deposited on the ground and latrines. Contaminants from these sources are mobilized and transported by recharge and lixiviation from rising groundwater levels. Piezometric data monitoring at 70 sites was conducted monthly from March 2004 to February 2005 to evaluate the seasonal variability of groundwater levels. Groundwater samples for chemical data were collected from the major aquifers in 74 dug wells, 14 boreholes and 1 spring for 2 years (232 samples in 4 campaigns). Data were also compiled from previous studies on groundwater, rain water, surface waters, latrines and soils. Geochemical data (major ions) are used to define groundwater groups, to map their distribution in the study area, and to evaluate their origin. We combined multivariate statistical methods, scatter diagrams, ionic ratios, and Piper diagrams to decipher the processes affecting the water chemistry at large (Niamey) and local (wells) scale. The piezometric time series revealed seasonal variability in all wells indicating that the study area is a recharge zone, which enhances the transfer of contaminants from the surface. The geochemical monitoring revealed high spatial and temporal variability in chemical parameters. Processes controlling the groundwater chemistry at large scales in the aquifers include atmospheric inputs (rainfall and dust) in the poorly mineralized formations, evapotranspiration in the soil layers, and alteration of silicates. Processes specific to individual wells are production of weak acids (H2CO3) and bases (HCO3-) in soil layers near pollutant sources, leaching of ions (Ca2+, Mg2+, Na+, K+, NH4+, NO3-, Cl-, HCO3-, SO42-) from pollutants, ion exchange

Calcite raft geochemistry as a hydrological proxy for Holocene aquifer conditions in Hoyo Negro and Ich Balam (Sac Actun Cave System), Quintana Roo, Mexico

Science.gov (United States)

Kovacs, Shawn E.; Reinhardt, Eduard G.; Chatters, James C.; Rissolo, Dominique; Schwarcz, Henry P.; Collins, Shawn V.; Kim, Sang-Tae; Nava Blank, Alberto; Luna Erreguerena, Pilar

2017-11-01

Two cores from calcite rafts deposits located in Cenote Ich Balam and Hoyo Negro were dated and analyzed for 87Sr/86Sr, δ18O, δ13C, Sr/Ca and Cl/Ca. The geochemical records show changing aquifer salinity spanning the last ∼ 8.5 cal kyrs BP and interrelationships with Holocene climate trends (wet and dry periods). During the wet mid-Holocene, the salinity of the meteoric Water Mass (WM; at 7.8-8.3 cal kyrs BP) was relatively high at 1.5-2.7 ppt and then became less saline (1.0-1.5 ppt) during the last ∼ 7000 yrs as climate became progressively drier. High salinity of the meteoric WM during the wet mid-Holocene is attributed to increased turbulent mixing between the meteoric and underlying marine WM. Increased precipitation, in terms of amount, frequency, and intensity (e.g. hurricanes) causes higher flow of meteoric water towards the coast and mixing at the halocline, a phenomenon recorded with recent instrumental monitoring of the aquifer. Conversely, during dry periods reduced precipitation and flow in the meteoric WM would result in lower salinity. Karst properties and Holocene sea-level rise also seem to have an effect on the aquifer. When the regionally extensive network of shallow cave passages (∼ 10-12 m water depth) are flooded at ∼ 8000 cal yrs BP, there is a rapid shift in salinity. This study demonstrates that calcite raft deposits can be used as paleo-environmental recorders documenting the effects of sea level and climate change on aquifer condition.

Geochemical modelling of worst-case leakage scenarios at potential CO2-storage sites - CO2 and saline water contamination of drinking water aquifers

Science.gov (United States)

Szabó, Zsuzsanna; Edit Gál, Nóra; Kun, Éva; Szőcs, Teodóra; Falus, György

2017-04-01

Carbon Capture and Storage is a transitional technology to reduce greenhouse gas emissions and to mitigate climate change. Following the implementation and enforcement of the 2009/31/EC Directive in the Hungarian legislation, the Geological and Geophysical Institute of Hungary is required to evaluate the potential CO2 geological storage structures of the country. Basic assessment of these saline water formations has been already performed and the present goal is to extend the studies to the whole of the storage complex and consider the protection of fresh water aquifers of the neighbouring area even in unlikely scenarios when CO2 injection has a much more regional effect than planned. In this work, worst-case scenarios are modelled to understand the effects of CO2 or saline water leaks into drinking water aquifers. The dissolution of CO2 may significantly change the pH of fresh water which induces mineral dissolution and precipitation in the aquifer and therefore, changes in solution composition and even rock porosity. Mobilization of heavy metals may also be of concern. Brine migration from CO2 reservoir and replacement of fresh water in the shallower aquifer may happen due to pressure increase as a consequence of CO2 injection. The saline water causes changes in solution composition which may also induce mineral reactions. The modelling of the above scenarios has happened at several methodological levels such as equilibrium batch, kinetic batch and kinetic reactive transport simulations. All of these have been performed by PHREEQC using the PHREEQC.DAT thermodynamic database. Kinetic models use equations and kinetic rate parameters from the USGS report of Palandri and Kharaka (2004). Reactive transport modelling also considers estimated fluid flow and dispersivity of the studied formation. Further input parameters are the rock and the original ground water compositions of the aquifers and a range of gas-phase CO2 or brine replacement ratios. Worst-case scenarios

Aquifer thermal-energy-storage modeling

Science.gov (United States)

Schaetzle, W. J.; Lecroy, J. E.

1982-09-01

A model aquifer was constructed to simulate the operation of a full size aquifer. Instrumentation to evaluate the water flow and thermal energy storage was installed in the system. Numerous runs injecting warm water into a preconditioned uniform aquifer were made. Energy recoveries were evaluated and agree with comparisons of other limited available data. The model aquifer is simulated in a swimming pool, 18 ft by 4 ft, which was filled with sand. Temperature probes were installed in the system. A 2 ft thick aquifer is confined by two layers of polyethylene. Both the aquifer and overburden are sand. Four well configurations are available. The system description and original tests, including energy recovery, are described.

Beryllium in river baseflow, shallow groundwaters and major aquifers of the U.K

International Nuclear Information System (INIS)

Edmunds, W.M.; Trafford, J.M.

1993-01-01

Out of 924 samples from 13 aquifer units in the United Kingdom, Be was detected in only 12. In carbonate aquifers no Be was found above the detection limit of 0.05 μg/1. The occurrence of Be was restricted to arenaceous aquifers where concentrations up to 1 μg/1 were found mainly in the Carboniferous Millstone Grit and Lower Cretaceous Lower Greensand. Interstitial water profiles from the unsaturated zones of the Lower Greensand and Triassic sandstone contain Be concentrations in excess of 10 μg/1 within the top 10 m which may persist to the water table at concentrations near to 1 μg/1. The only major anomaly to be found in river baseflow was from the Mourne Mountains of Northern Ireland where Be concentrations of up to 4.7 μg/1 were found associated with the outcrop of the Tertiary granite intrusion. Elsewhere, Be (0.22 μg/1) was found in neutral groundwaters derived from granite feeding the acid Loch Fleet (southern Scotland) in which concentrations of 0.09 μg/1 were maintained. Beryllium occurrence therefore depends strongly on geology. The predominant aqueous species below pH 5.5 is Be 2+ and above this Be(OH) + dominates. The presence of high Al in most waters sampled greatly suppresses the formation of BeF complex ions. Beryllium shows close geochemical behaviour with Mg across a range of pH which may have environmental consequences, if Be substitution for Mg takes place. (author)

Remediation of a contaminated thin aquifer by horizontal wells

Energy Technology Data Exchange (ETDEWEB)

Breh, W.; Suttheimer, J.; Hoetzl, H. [Univ. of Karlsruhe (Germany); Frank, K. [GEO-Service GmbH, Rheinmuenster (Germany)

1997-12-31

At an industrial site in Bruchsal (Germany) a huge trichloroethene contamination was found. After common remedial actions proved to be widely ineffective, new investigations led to a highly contaminated thin aquifer above the main aquifer. The investigation and the beginning of the remediation of the thin aquifer by two horizontal wells is described in this paper. Special attention was given to the dependence between precipitation and the flow direction in the thin aquifer and to hydraulic connections between the thin and the main aquifer. Also a short introduction into a new remedial technique by horizontal wells and first results of the test phase of the horizontal wells are given.

Groundwater vulnerability mapping in Guadalajara aquifers system (Western Mexico)

Science.gov (United States)

Rizo-Decelis, L. David; Marín, Ana I.; Andreo, Bartolomé

2016-04-01

Groundwater vulnerability mapping is a practical tool to implement strategies for land-use planning and sustainable socioeconomic development coherent with groundwater protection. The objective of vulnerability mapping is to identify the most vulnerable zones of catchment areas and to provide criteria for protecting the groundwater used for drinking water supply. The delineation of protection zones in fractured aquifers is a challenging task due to the heterogeneity and anisotropy of hydraulic conductivities, which makes difficult prediction of groundwater flow organization and flow velocities. Different methods of intrinsic groundwater vulnerability mapping were applied in the Atemajac-Toluquilla groundwater body, an aquifers system that covers around 1300 km2. The aquifer supplies the 30% of urban water resources of the metropolitan area of Guadalajara (Mexico), where over 4.6 million people reside. Study area is located in a complex neotectonic active volcanic region in the Santiago River Basin (Western Mexico), which influences the aquifer system underneath the city. Previous works have defined the flow dynamics and identified the origin of recharge. In addition, the mixture of fresh groundwater with hydrothermal and polluted waters have been estimated. Two main aquifers compose the multilayer system. The upper aquifer is unconfined and consists of sediments and pyroclastic materials. Recharge of this aquifer comes from rainwater and ascending vertical fluids from the lower aquifer. The lower aquifer consists of fractured basalts of Pliocene age. Formerly, the main water source has been the upper unit, which is a porous and unconsolidated unit, which acts as a semi-isotropic aquifer. Intense groundwater usage has resulted in lowering the water table in the upper aquifer. Therefore, the current groundwater extraction is carried out from the deeper aquifer and underlying bedrock units, where fracture flow predominates. Pollution indicators have been reported in

Assessment of microbial in situ activity in contaminated aquifers

Energy Technology Data Exchange (ETDEWEB)

Kaestner, M. [UFZ-Umweltforschungszentrum Leipzig-Halle GmbH, Department Bioremediation, Permoserstrasse 15, 04318 Leipzig (Germany); Fischer, A.; Nijenhuis, I.; Stelzer, N.; Bombach, P.; Richnow, H.H. [UFZ-Umweltforschungszentrum Leipzig-Halle GmbH, Department Isotopenbiogeochemie, Permoserstrasse 15, 04318 Leipzig (Germany); Geyer, R. [UFZ-Umweltforschungszentrum Leipzig-Halle GmbH, Department Umweltmikrobiologie, Permoserstrasse 15, 04318 Leipzig (Germany); Tebbe, C.C. [Institut fuer Agraroekologie, Bundesforschungsanstalt fuer Landwirtschaft (FAL), D-38116 Braunschweig (Germany)

2006-06-15

Microbial ecologists and environmental engineers share the interest in identifying the key microorganisms responsible for compound turnover in the environment and in estimating the respective transformation rates. For the successful application of Natural Attenuation processes, a reliable assessment of the in situ turnover of a contaminant in an aquifer is essential. Here, we review and present new details of two recently developed approaches concerning the assessment of in situ biodegradation: (i) determination of biodegradation caused by microbial metabolism in a contamination plume by stable isotope fractionation analysis (SIFA) and (ii) determination of the actual degradation under the respective environmental conditions in the aquifer by using in situ microcosms (BACTRAPS registered) amended with {sup 13}C-labeled substrates as tracer compounds. Based on stable isotope fractionation analysis, the degradation occurring under anoxic biogeochemical conditions at a respective site can be calculated for the entire plume. This has been shown for benzene and toluene at the Zeitz site and partly for chlorobenzene at the Bitterfeld site. By use of the in situ microcosm approach with {sup 13}C-labeled compounds, the microbial in situ degradation under strictly anaerobic conditions could be proven for benzene and toluene in Zeitz and for chlorobenzene in Bitterfeld. The transformation of {sup 13}C-carbon of the labeled substrate into microbial fatty acids confirmed the assimilation of the pollutant resulting in the formation of biomass. In addition, metabolites such as benzylsuccinic acid were found in the toluene-amended microcosms indicating anaerobic degradation of toluene. This result corresponds to the geochemical conditions found at the field site and therefore, the microcosm approach with {sup 13}C-labeled compounds can be used to assign the predominant in situ degradation pathways in a contaminated aquifer. Since fatty acids profiles alone are often too

Geochemical features and effects on deep-seated fluids during the May-June 2012 southern Po Valley seismic sequence

Directory of Open Access Journals (Sweden)

Francesco Italiano

2012-10-01

Full Text Available A periodic sampling of the groundwaters and dissolved and free gases in selected deep wells located in the area affected by the May-June 2012 southern Po Valley seismic sequence has provided insight into seismogenic-induced changes of the local aquifer systems. The results obtained show progressive changes in the fluid geochemistry, allowing it to be established that deep-seated fluids were mobilized during the seismic sequence and reached surface layers along faults and fractures, which generated significant geochemical anomalies. The May-June 2012 seismic swarm (mainshock on May 29, 2012, M 5.8; 7 shocks M >5, about 200 events 3 > M > 5 induced several modifications in the circulating fluids. This study reports the preliminary results obtained for the geochemical features of the waters and gases collected over the epicentral area from boreholes drilled at different depths, thus intercepting water and gases with different origins and circulation. The aim of the investigations was to improve our knowledge of the fluids circulating over the seismic area (e.g. origin, provenance, interactions, mixing of different components, temporal changes. This was achieved by collecting samples from both shallow and deep-drilled boreholes, and then, after the selection of the relevant sites, we looked for temporal changes with mid-to-long-term monitoring activity following a constant sampling rate. This allowed us to gain better insight into the relationships between the fluid circulation and the faulting activity. The sampling sites are listed in Table 1, along with the analytical results of the gas phase. […

Geochemical controls on shale groundwaters: Results of reaction path modeling

International Nuclear Information System (INIS)

Von Damm, K.L.; VandenBrook, A.J.

1989-03-01

The EQ3NR/EQ6 geochemical modeling code was used to simulate the reaction of several shale mineralogies with different groundwater compositions in order to elucidate changes that may occur in both the groundwater compositions, and rock mineralogies and compositions under conditions which may be encountered in a high-level radioactive waste repository. Shales with primarily illitic or smectitic compositions were the focus of this study. The reactions were run at the ambient temperatures of the groundwaters and to temperatures as high as 250/degree/C, the approximate temperature maximum expected in a repository. All modeling assumed that equilibrium was achieved and treated the rock and water assemblage as a closed system. Graphite was used as a proxy mineral for organic matter in the shales. The results show that the presence of even a very small amount of reducing mineral has a large influence on the redox state of the groundwaters, and that either pyrite or graphite provides essentially the same results, with slight differences in dissolved C, Fe and S concentrations. The thermodynamic data base is inadequate at the present time to fully evaluate the speciation of dissolved carbon, due to the paucity of thermodynamic data for organic compounds. In the illitic cases the groundwaters resulting from interaction at elevated temperatures are acid, while the smectitic cases remain alkaline, although the final equilibrium mineral assemblages are quite similar. 10 refs., 8 figs., 15 tabs

Determination of {sup 222}Rn and its physico-chemical and biological characteristics in aquifers of Toluca valley; Determinacion de {sup 222}Rn y caracteristicas fisicoquimicas y biologicas en acuiferos del Valle de Toluca

Energy Technology Data Exchange (ETDEWEB)

Hernandez, A.; Aranda, P.; Ceballos, S.; Cruz, D.; Jauregui, B.; Lopez, R.; Pena, P.; Salazar, S.; Segovia, N.; Tamez, E. [Instituto nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico)

1997-07-01

In this work it is realized a geochemical study which includes the evaluation of {sup 222} Rn concentration in drinking water wells at Toluca city and a spring water of Almoloya de Juarez municipality at State of mexico. the same is studied about evolution of {sup 222} Rn concentration in water of the hydrating which supply it to those wells. the geochemical evaluation also covers the determination of major and minor elements or trace and the biological analysis of water. The study includes two seasonal cycles, the low water mark one and other the rainy for being able to evaluate the aquifers reloading effects in the water composition. (Author)

Groundwaters of Florence (Italy): Trace element distribution and vulnerability of the aquifers

Energy Technology Data Exchange (ETDEWEB)

Bencini, A.; Ercolanelli, R.; Sbaragli, A. [Univ. of Florence (Italy)] [and others

1993-11-01

Geochemical and hydrogeological research has been carried out in Florence, to evaluate conductivity and main chemistry of groundwaters, the pattern of some possible pollutant chemical species (Fe, Mn, Cr, Cu, Pb, Zn, NO{sub 2}, NO{sub 3}), and the vulnerability of the aquifers. The plain is made up of Plio-Quaternary alluvial and lacustrine sediments for a maximum thickness of 600 m. Silts and clays, sometimes with lenses of sandy gravels, are dominant, while considerable deposits of sands, pebbles, and gravels occur along the course of the Arno river and its tributary streams, and represent the most important aquifer of the plain. Most waters show conductivity values around 1000-1200 {mu}S, and almost all of them have an alkaline-earth-bicarbonate chemical character. In western areas higher salt content of the groundwaters is evident. Heavy metal and NO{sub 2}, NO{sub 3} analyses point out that no important pollution phenomena affect the groundwaters; all mean values are below the maximum admissible concentration (MAC) for drinkable waters. Some anomalies of NO{sub 2}, NO{sub 3}, Fe, Mn, and Zn are present. The most plausible causes can be recognized in losses of the sewage system; use of nitrate compounds in agriculture; oxidation of well pipes. All the observations of Cr, Cu, and Pb are below the MAC; the median values of <3, 3.9, and 1.1 {mu}g/l, respectively, could be considered reference concentrations for groundwaters in calcareous lithotypes, under undisturbed natural conditions. Finally, a map of vulnerability shows that the areas near the Arno river are highly vulnerable, for the minimum thickness (or lacking) of sediments covering the aquifer. On the other hand, in the case of pollution, several factors not considered could significantly increase the self-purification capacity of the aquifer, such asdilution of groundwaters, bacteria oxidation of nitrogenous species, and sorption capacity of clay minerals and organic matter. 31 refs., 6 figs., 5 tabs.

Investigation by multivariate analysis of groundwater composition in a multilayer aquifer system from North Africa: A multi-tracer approach

Energy Technology Data Exchange (ETDEWEB)

Dassi, Lassaad, E-mail: lassaad@geologist.com [Faculte des Sciences, Departement des Sciences de la Terre, Zrig, Gabes 6072 (Tunisia)

2011-08-15

Highlights: > We investigate the hydrodynamics and hydrochemistry of a multilayer aquifer system. > We examine the geochemical evolution, the origins and the circulation patterns of groundwater. > The mineralization is controlled by water-rock interaction and return flow process. > Groundwater derives from palaeoclimatic and modern end-members. > Mixing by upward and downward leakage occurs between these two end-members. - Abstract: A multi-tracer approach has been carried out in the Sbeitla multilayer aquifer system, central Tunisia, to investigate the geochemical evolution, the origin of groundwaters and their circulation patterns. It involves statistical data analysis coupled with the definition of the hydrochemical and isotopic features of the different groundwaters. Principal Components Analysis (PCA) of geochemical data used in conjunction with bivariate diagrams of major and trace elements indicate that groundwater mineralization is mainly controlled by water-rock interaction and anthropogenic processes in relation to return flow of irrigation waters. The PCA of isotopic data and bivariate conventional diagrams of stable and radiogenic isotopes i.e. {delta}{sup 18}O vs. {delta}{sup 2}H and {delta}{sup 18}O vs. {sup 14}C provide valuable information about the origin and the circulation patterns of the different groundwater groups. They permit classifying groundwaters into three groups. The first group is characterized by low {sup 3}H concentrations, low {sup 14}C activities and depleted stable isotope contents. It corresponds to an old end-member in relation with palaeoclimatic recharge which occurred during the Late Pleistocene and the Early Holocene humid periods. The second group is distinguished by high to moderate {sup 3}H concentrations, high {sup 14}C activities and enriched heavy isotope signatures. It corresponds to a modern end-member originating from a mixture of post-nuclear and present-day recharge in relation to return flow of irrigation waters

Impacts of geochemical and environmental factors on seasonal variation of heavy metals in a coastal lagoon Yucatan, Mexico.

Science.gov (United States)

Arcega-Cabrera, F; Garza-Pérez, R; Noreña-Barroso, E; Oceguera-Vargas, I

2015-01-01

This study investigated the influence of geochemical and environmental factors on seasonal variation in metals in Yucatan's Chelem lagoon. Anthropogenic activities discharge non-treated wastewater directly into it with detrimental environmental consequences. Accordingly, this study established the spatial and temporal patterns of fine grain sediments and concentrations of heavy metals. Multivariate analyses showed fine grain facies deposition, transition sites dominated by fine grain transport, and fine grain erosion sites. Spatial and temporal variations of heavy metals concentration were significant for Cd, Cu, Cr, and Pb. As, Cd, and Sn were as much as 12 times higher than SQuiRTs standards (Buchman 2008). The results indicate that aquifer water is bringing metals from relatively far inland and releasing them into the lagoon. Thus, it appears that the contamination of this lagoon is highly complex and must take into account systemic connections with inland anthropogenic activates and pollution, as well as local factors.

Predicted nitrate and arsenic concentrations in basin-fill aquifers of the Southwestern United States

Science.gov (United States)

Anning, David W.; Paul, Angela P.; McKinney, Tim S.; Huntington, Jena M.; Bexfield, Laura M.; Thiros, Susan A.

2012-01-01

The National Water-Quality Assessment (NAWQA) Program of the U.S. Geological Survey (USGS) is conducting a regional analysis of water quality in the principal aquifer systems across the United States. The Southwest Principal Aquifers (SWPA) study is building a better understanding of the susceptibility and vulnerability of basin-fill aquifers in the region to groundwater contamination by synthesizing baseline knowledge of groundwater-quality conditions in 16 basins previously studied by the NAWQA Program. The improved understanding of aquifer susceptibility and vulnerability to contamination is assisting in the development of tools that water managers can use to assess and protect the quality of groundwater resources.Human-health concerns and economic considerations associated with meeting drinking-water standards motivated a study of the vulnerability of basin-fill aquifers to nitrate con­tamination and arsenic enrichment in the southwestern United States. Statistical models were developed by using the random forest classifier algorithm to predict concentrations of nitrate and arsenic across a model grid that represents about 190,600 square miles of basin-fill aquifers in parts of Arizona, California, Colorado, Nevada, New Mexico, and Utah. The statistical models, referred to as classifiers, reflect natural and human-related factors that affect aquifer vulnerability to contamina­tion and relate nitrate and arsenic concentrations to explana­tory variables representing local- and basin-scale measures of source, aquifer susceptibility, and geochemical conditions. The classifiers were unbiased and fit the observed data well, and misclassifications were primarily due to statistical sampling error in the training datasets.The classifiers were designed to predict concentrations to be in one of six classes for nitrate, and one of seven classes for arsenic. Each classification scheme allowed for identification of areas with concentrations that were equal to or exceeding

Genesis and evolution of the fumaroles of vulcano (Aeolian Islands, Italy): a geochemical model

Science.gov (United States)

Carapezza, M.; Nuccio, P. M.; Valenza, M.

1981-09-01

A geochemical model explaining the presence of fumaroles having different gas composition and temperature at the top of the crater and along the northeastern coast of Vulcano island is proposed. A pressurized biphase (liquid-vapor) reservoir at the depth of about 2 km is hypothesized. Energy and mass balance sheets control P-T conditions in the system. P-T must vary along a boiling curve of brine as liquid is present. The CO2 content in the steam is governed by the thermodynamic properties of the fluids in the H2-NaCl-CO2 system. On the assumption that oxygen fugacity in the system is between the HM-FMQ oxygen buffers, observed SO2/H2S, CO2/CO, CO/CH4 ratios in the fumarolic gases at the Fossa crater appear in equilibrium with a temperature higher than that observed, such as may exist at depth. The more reduced gas phases present on the sea-side may result from re-equilibrium processes in shallower aquifers. The suggested model would help in monitoring changes in volcanic activity by analyzing fumarolic gases.

Anoxic nitrate reduction coupled with iron oxidation and attenuation of dissolved arsenic and phosphate in a sand and gravel aquifer

Science.gov (United States)

Smith, Richard L.; Kent, Douglas B.; Repert, Deborah A.; Böhlke, J.K.

2017-01-01

Nitrate has become an increasingly abundant potential electron acceptor for Fe(II) oxidation in groundwater, but this redox couple has not been well characterized within aquifer settings. To investigate this reaction and some of its implications for redox-sensitive groundwater contaminants, we conducted an in situ field study in a wastewater-contaminated aquifer on Cape Cod. Long-term (15 year) geochemical monitoring within the contaminant plume indicated interacting zones with variable nitrate-, Fe(II)-, phosphate-, As(V)-, and As(III)-containing groundwater. Nitrate and phosphate were derived predominantly from wastewater disposal, whereas Fe(II), As(III), and As(V) were mobilized from the aquifer sediments. Multiple natural gradient, anoxic tracer tests were conducted in which nitrate and bromide were injected into nitrate-free, Fe(II)-containing groundwater. Prior to injection, aqueous Fe(II) concentrations were approximately 175 μM, but sorbed Fe(II) accounted for greater than 90% of the total reactive Fe(II) in the aquifer. Nitrate reduction was stimulated within 1 m of transport for 100 μM and 1000 μM nitrate additions, initially producing stoichiometric quantities of nitrous oxide (>300 μM N). In subsequent injections at the same site, nitrate was reduced even more rapidly and produced less nitrous oxide, especially over longer transport distances. Fe(II) and nitrate concentrations decreased together and were accompanied by Fe(III) oxyhydroxide precipitation and decreases in dissolved phosphate, As(III), and As(V) concentrations. Nitrate N and O isotope fractionation effects during nitrate reduction were approximately equal (ε15N/ε18O = 1.11) and were similar to those reported for laboratory studies of biological nitrate reduction, including denitrification, but unlike some reported effects on nitrate by denitrification in aquifers. All constituents affected by the in situ tracer experiments returned to pre-injection levels after several

Geophysical Monitoring of Coupled Microbial and Geochemical Processes During Stimulated Subsurface Bioremediation

International Nuclear Information System (INIS)

Williams, Kenneth H.; Kemna, Andreas; Wilkins, Michael J.; Druhan, Jennifer L.; Arntzen, Evan V.; N'Guessan, A. Lucie; Long, Philip E.; Hubbard, Susan S.; Banfield, Jillian F.

2009-01-01

Understanding how microorganisms alter their physical and chemical environment during bioremediation is hindered by our inability to resolve subsurface microbial activity with high spatial resolution. Here we demonstrate the use of a minimally invasive geophysical technique to monitor stimulated microbial activity during acetate amendment in an aquifer near Rifle, Colorado. During electrical induced polarization (IP) measurements, spatiotemporal variations in the phase response between imposed electric current and the resultant electric field correlated with changes in groundwater geochemistry accompanying stimulated iron and sulfate reduction and sulfide mineral precipitation. The magnitude of the phase response varied with measurement frequency (0.125 and 1 Hz) and was dependent upon the dominant metabolic process. The spectral effect was corroborated using a biostimulated column experiment containing Rifle sediments and groundwater. Fluids and sediments recovered from regions exhibiting an anomalous phase response were enriched in Fe(II), dissolved sulfide, and cell-associated FeS nanoparticles. The accumulation of mineral precipitates and electroactive ions altered the ability of pore fluids to conduct electrical charge, accounting for the anomalous IP response and revealing the usefulness of multifrequency IP measurements for monitoring mineralogical and geochemical changes accompanying stimulated subsurface bioremediation

Ground-water quality of the surficial aquifer system and the upper Floridan Aquifer, Ocala National Forest and Lake County, Florida, 1990-99

Science.gov (United States)

Adamski, J.C.; Knowles, Leel

2001-01-01

Data from 217 ground-water samples were statistically analyzed to assess the water quality of the surficial aquifer system and Upper Floridan aquifer in the Ocala National Forest and Lake County, Florida. Samples were collected from 49 wells tapping the surficial aquifer system, 141 wells tapping the Upper Floridan aquifer, and from 27 springs that discharge water from the Upper Floridan aquifer. A total of 136 samples was collected by the U.S. Geological Survey from 1995 through 1999. These data were supplemented with 81 samples collected by the St. Johns River Water Management District and Lake County Water Resources Management from 1990 through 1998. In general, the surficial aquifer system has low concentrations of total dissolved solids (median was 41 milligrams per liter) and major ions. Water quality of the surficial aquifer system, however, is not homogeneous throughout the study area. Concentrations of total dissolved solids, many major ions, and nutrients are greater in samples from Lake County outside the Ocala National Forest than in samples from within the Forest. These results indicate that the surficial aquifer system in Lake County outside the Ocala National Forest probably is being affected by agricultural and (or) urban land-use practices. High concentrations of dissolved oxygen (less than 0.1 to 8.2 milligrams per liter) in the surficial aquifer system underlying the Ocala National Forest indicate that the aquifer is readily recharged by precipitation and is susceptible to surface contamination. Concentrations of total dissolved solids were significantly greater in the Upper Floridan aquifer (median was 182 milligrams per liter) than in the surficial aquifer system. In general, water quality of the Upper Floridan aquifer was homogeneous, primarily being a calcium or calciummagnesium- bicarbonate water type. Near the St. Johns River, the water type of the Upper Floridan aquifer is sodium-chloride, corresponding to an increase in total dissolved

Assessment of managed aquifer recharge at Sand Hollow Reservoir, Washington County, Utah, updated to conditions through 2014

Science.gov (United States)

Marston, Thomas M.; Heilweil, Victor M.

2016-09-08

Sand Hollow Reservoir in Washington County, Utah, was completed in March 2002 and is operated primarily for managed aquifer recharge by the Washington County Water Conservancy District. From 2002 through 2014, diversions of about 216,000 acre-feet from the Virgin River to Sand Hollow Reservoir have allowed the reservoir to remain nearly full since 2006. Groundwater levels in monitoring wells near the reservoir rose through 2006 and have fluctuated more recently because of variations in reservoir stage and nearby pumping from production wells. Between 2004 and 2014, about 29,000 acre-feet of groundwater was withdrawn by these wells for municipal supply. In addition, about 31,000 acre-feet of shallow seepage was captured by French drains adjacent to the North and West Dams and used for municipal supply, irrigation, or returned to the reservoir. From 2002 through 2014, about 127,000 acre-feet of water seeped beneath the reservoir to recharge the underlying Navajo Sandstone aquifer.Water quality continued to be monitored at various wells in Sand Hollow during 2013–14 to evaluate the timing and location of reservoir recharge as it moved through the aquifer. Changing geochemical conditions at monitoring wells WD 4 and WD 12 indicate rising groundwater levels and mobilization of vadose-zone salts, which could be a precursor to the arrival of reservoir recharge.

Source, variability, and transformation of nitrate in a regional karst aquifer: Edwards aquifer, central Texas

Energy Technology Data Exchange (ETDEWEB)

Musgrove, M., E-mail: mmusgrov@usgs.gov [U.S. Geological Survey, 1505 Ferguson Lane, Austin, TX 78754 (United States); Opsahl, S.P. [U.S. Geological Survey, 5563 DeZavala, Ste. 290, San Antonio, TX 78249 (United States); Mahler, B.J. [U.S. Geological Survey, 1505 Ferguson Lane, Austin, TX 78754 (United States); Herrington, C. [City of Austin Watershed Protection Department, Austin, TX 78704 (United States); Sample, T.L. [U.S. Geological Survey, 19241 David Memorial Dr., Ste. 180, Conroe, TX 77385 (United States); Banta, J.R. [U.S. Geological Survey, 5563 DeZavala, Ste. 290, San Antonio, TX 78249 (United States)

2016-10-15

Many karst regions are undergoing rapid population growth and expansion of urban land accompanied by increases in wastewater generation and changing patterns of nitrate (NO{sub 3}{sup −}) loading to surface and groundwater. We investigate variability and sources of NO{sub 3}{sup −} in a regional karst aquifer system, the Edwards aquifer of central Texas. Samples from streams recharging the aquifer, groundwater wells, and springs were collected during 2008–12 from the Barton Springs and San Antonio segments of the Edwards aquifer and analyzed for nitrogen (N) species concentrations and NO{sub 3}{sup −} stable isotopes (δ{sup 15}N and δ{sup 18}O). These data were augmented by historical data collected from 1937 to 2007. NO{sub 3}{sup −} concentrations and discharge data indicate that short-term variability (days to months) in groundwater NO{sub 3}{sup −} concentrations in the Barton Springs segment is controlled by occurrence of individual storms and multi-annual wet-dry cycles, whereas the lack of short-term variability in groundwater in the San Antonio segment indicates the dominance of transport along regional flow paths. In both segments, longer-term increases (years to decades) in NO{sub 3}{sup −} concentrations cannot be attributed to hydrologic conditions; rather, isotopic ratios and land-use change indicate that septic systems and land application of treated wastewater might be the source of increased loading of NO{sub 3}{sup −}. These results highlight the vulnerability of karst aquifers to NO{sub 3}{sup −} contamination from urban wastewater. An analysis of N-species loading in recharge and discharge for the Barton Springs segment during 2008–10 indicates an overall mass balance in total N, but recharge contains higher concentrations of organic N and lower concentrations of NO{sub 3}{sup −} than does discharge, consistent with nitrification of organic N within the aquifer and consumption of dissolved oxygen. This study demonstrates

Source, variability, and transformation of nitrate in a regional karst aquifer: Edwards aquifer, central Texas

International Nuclear Information System (INIS)

Musgrove, M.; Opsahl, S.P.; Mahler, B.J.; Herrington, C.; Sample, T.L.; Banta, J.R.

2016-01-01

Many karst regions are undergoing rapid population growth and expansion of urban land accompanied by increases in wastewater generation and changing patterns of nitrate (NO 3 − ) loading to surface and groundwater. We investigate variability and sources of NO 3 − in a regional karst aquifer system, the Edwards aquifer of central Texas. Samples from streams recharging the aquifer, groundwater wells, and springs were collected during 2008–12 from the Barton Springs and San Antonio segments of the Edwards aquifer and analyzed for nitrogen (N) species concentrations and NO 3 − stable isotopes (δ 15 N and δ 18 O). These data were augmented by historical data collected from 1937 to 2007. NO 3 − concentrations and discharge data indicate that short-term variability (days to months) in groundwater NO 3 − concentrations in the Barton Springs segment is controlled by occurrence of individual storms and multi-annual wet-dry cycles, whereas the lack of short-term variability in groundwater in the San Antonio segment indicates the dominance of transport along regional flow paths. In both segments, longer-term increases (years to decades) in NO 3 − concentrations cannot be attributed to hydrologic conditions; rather, isotopic ratios and land-use change indicate that septic systems and land application of treated wastewater might be the source of increased loading of NO 3 − . These results highlight the vulnerability of karst aquifers to NO 3 − contamination from urban wastewater. An analysis of N-species loading in recharge and discharge for the Barton Springs segment during 2008–10 indicates an overall mass balance in total N, but recharge contains higher concentrations of organic N and lower concentrations of NO 3 − than does discharge, consistent with nitrification of organic N within the aquifer and consumption of dissolved oxygen. This study demonstrates that subaqueous nitrification of organic N in the aquifer, as opposed to in soils, might be a

Aquifer test to determine hydraulic properties of the Elm aquifer near Aberdeen, South Dakota

Science.gov (United States)

Schaap, Bryan D.

2000-01-01

The Elm aquifer, which consists of sandy and gravelly glacial-outwash deposits, is present in several counties in northeastern South Dakota. An aquifer test was conducted northeast of Aberdeen during the fall of 1999 to determine the hydraulic properties of the Elm aquifer in that area. An improved understanding of the properties of the aquifer will be useful in the possible development of the aquifer as a water resource. Historical water-level data indicate that the saturated thickness of the Elm aquifer can change considerably over time. From September 1977 through November 1985, water levels at three wells completed in the Elm aquifer near the aquifer test site varied by 5.1 ft, 9.50 ft, and 11.1 ft. From June 1982 through October 1999, water levels at five wells completed in the Elm aquifer near the aquifer test site varied by 8.7 ft, 11.4 ft, 13.2 ft, 13.8 ft, and 19.7 ft. The water levels during the fall of 1999 were among the highest on record, so the aquifer test was affected by portions of the aquifer being saturated that might not be saturated during drier times. The aquifer test was conducted using five existing wells that had been installed prior to this study. Well A, the pumped well, has an operating irrigation pump and is centrally located among the wells. Wells B, C, D, and E are about 70 ft, 1,390 ft, 2,200 ft, and 3,100 ft, respectively, in different directions from Well A. Using vented pressure transducers and programmable data loggers, water-level data were collected at the five wells prior to, during, and after the pumping, which started on November 19, 1999, and continued a little over 72 hours. Based on available drilling logs, the Elm aquifer near the test area was assumed to be unconfined. The Neuman (1974) method theoretical response curves that most closely match the observed water-level changes at Wells A and B were calculated using software (AQTESOLV for Windows Version 2.13-Professional) developed by Glenn M. Duffield of Hydro

Effects of a Reservoir Water on the GW Quality in a Coastal Aquifer of Semi-arid Region, North-east of Tunisia

Science.gov (United States)

Uchida, C.; Kawachi, A.; Tsujimura, M.; Tarhouni, J.

2015-12-01

This study investigated effects of a reservoir water in a salinized shallow aquifer based on spatial distribution of geochemical properties in groundwater (GW). In many coastal shallow aquifers of arid and semi-arid regions, groundwater table (GWT) depression and salinization have occurred due to GW overexploitation. In Korba aquifer, north-east of Tunisia, after a dam reservoir has been constructed in order to assure a water resource for irrigation, improvement of GW level and quality have been observed in the downstream area of the dam (area-A), while the GW in the other area (area-B) still has high salinity. This study, therefore, aimed to investigate the effects of the reservoir water on the GW quality. In June 2013, water quality survey and sampling were carried out at 60 wells (GW), a dam reservoir, river and the sea. Major ions, boron, bromide, and oxygen-18 and deuterium in collected samples were analyzed. From the results, in the area-B, the GWT was lower than the sea level and the high salinity were observed. The Br- concentration of the GW was correlated with the Cl- concentration, and the values of B/Cl- and Br-/Cl- of the GW were similar to the seawater. Since the GWT depression allowed the seawater to intrude into the aquifer, the GW salinization occurred in this area. On the other hand, in the area-A, GWT was higher than the seawater level, and the Na+ and Cl- concentrations were lower than the area-B. Especially, in the irrigated areas by using the reservoir water, the isotopic values, B/Cl- and Br-/Cl- of the GW were relatively higher than the others. The reservoir water has high isotopic values due to evaporation effect, and the B/Cl- and Br-/Cl- values become higher due to organic matters in sediment of the reservoir or soil in the filtration process. Thus, in addition to the direct infiltration from the reservoir into the aquifer, irrigation using a reservoir water probably has a positive impact on the GW quality in this area.

Coupled geochemical and solute transport code development

International Nuclear Information System (INIS)

Morrey, J.R.; Hostetler, C.J.

1985-01-01

A number of coupled geochemical hydrologic codes have been reported in the literature. Some of these codes have directly coupled the source-sink term to the solute transport equation. The current consensus seems to be that directly coupling hydrologic transport and chemical models through a series of interdependent differential equations is not feasible for multicomponent problems with complex geochemical processes (e.g., precipitation/dissolution reactions). A two-step process appears to be the required method of coupling codes for problems where a large suite of chemical reactions must be monitored. Two-step structure requires that the source-sink term in the transport equation is supplied by a geochemical code rather than by an analytical expression. We have developed a one-dimensional two-step coupled model designed to calculate relatively complex geochemical equilibria (CTM1D). Our geochemical module implements a Newton-Raphson algorithm to solve heterogeneous geochemical equilibria, involving up to 40 chemical components and 400 aqueous species. The geochemical module was designed to be efficient and compact. A revised version of the MINTEQ Code is used as a parent geochemical code

Bioremediation of a diesel fuel contaminated aquifer: simulation studies in laboratory aquifer columns

Science.gov (United States)

Hess, A.; Höhener, P.; Hunkeler, D.; Zeyer, J.

1996-08-01

The in situ bioremediation of aquifers contaminated with petroleum hydrocarbons is commonly based on the infiltration of groundwater supplemented with oxidants (e.g., O 2, NO 3-) and nutrients (e.g., NH 4+, PO 43-). These additions stimulate the microbial activity in the aquifer and several field studies describing the resulting processes have been published. However, due to the heterogeneity of the subsurface and due to the limited number of observation wells usually available, these field data do not offer a sufficient spatial and temporal resolution. In this study, flow-through columns of 47-cm length equipped with 17 sampling ports were filled with homogeneously contaminated aquifer material from a diesel fuel contaminated in situ bioremediation site. The columns were operated over 96 days at 12°C with artificial groundwater supplemented with O 2, NO 3- and PO 43-. Concentration profiles of O 2, NO 3-, NO 2-, dissolved inorganic and organic carbon (DIC and DOC, respectively), protein, microbial cells and total residual hydrocarbons were measured. Within the first 12 cm, corresponding to a mean groundwater residence time of < 3.6 h, a steep O 2 decrease from 4.6 to < 0.3 mg l -1, denitrification, a production of DIC and DOC, high microbial cell numbers and a high removal of hydrocarbons were observed. Within a distance of 24 to 40.5 cm from the infiltration, O 2 was below 0.1 mg l -1 and a denitrifying activity was found. In the presence and in the absence of O 2, n-alkanes were preferentially degraded compared to branched alkanes. The results demonstrate that: (1) infiltration of aerobic groundwater into columns filled with aquifer material contaminated with hydrocarbons leads to a rapid depletion of O 2; (2) O 2 and NO 3- can serve as oxidants for the mineralization of hydrocarbons; and (3) the modelling of redox processes in aquifers has to consider denitrifying activity in presence of O 2.

Mapping of coastal aquifer vulnerable zone in the south west coast of Kanyakumari, South India, using GIS-based DRASTIC model.

Science.gov (United States)

Kaliraj, S; Chandrasekar, N; Peter, T Simon; Selvakumar, S; Magesh, N S

2015-01-01

The south west coast of Kanyakumari district in Tamil Nadu, India, is significantly affected by seawater intrusion and diffusion of pollutants into the aquifers due to unregulated beach placer mining and other anthropogenic activities. The present study investigates the vulnerability of the coastal aquifers using Geographic Information System (GIS)-based DRASTIC model. The seven DRASTIC parameters have been analyzed using the statistical equation of this model to demarcate the vulnerable zones for aquifer contamination. The vulnerability index map is prepared from the weighted spatial parameters, and an accounting of total index value ranged from 85 to 213. Based on the categorization of vulnerability classes, the high vulnerable zones are found near the beach placer mining areas between Manavalakurichi and Kodimanal coastal stretches. The aquifers associated with settlements and agricultural lands in the middle-eastern part have experienced high vulnerability due to contaminated water bodies. Similarly, the coastal areas of Thengapattinam and Manakudi estuary and around the South Tamaraikulam have also been falling under high vulnerability condition due to backwater and saltpan. In general, the nearshore region except the placer mining zone and the backwater has a moderately vulnerable condition, and the vulnerability index values range from 149 to180. Significantly, the northern and northeastern uplands and some parts of deposition zones in the middle-south coast have been identified as low to no vulnerable conditions. They are structurally controlled by various geological features such as charnockite, garnet biotite gneiss and granites, and sand dunes, respectively. The aquifer vulnerability assessment has been cross-verified by geochemical indicators such as total dissolved solids (TDS), Cl(-), HCO₃(-), and Cl(-)/HCO₃(-) ratio. The high ranges of TDS (1,842--3,736 mg/l) and Cl(-) (1,412--2,112 mg/l) values are well correlated with the observed high

Transient well flow in leaky multiple-aquifer systems

Science.gov (United States)

Hemker, C. J.

1985-10-01

A previously developed eigenvalue analysis approach to groundwater flow in leaky multiple aquifers is used to derive exact solutions for transient well flow problems in leaky and confined systems comprising any number of aquifers. Equations are presented for the drawdown distribution in systems of infinite extent, caused by wells penetrating one or more of the aquifers completely and discharging each layer at a constant rate. Since the solution obtained may be regarded as a combined analytical-numerical technique, a type of one-dimensional modelling can be applied to find approximate solutions for several complicating conditions. Numerical evaluations are presented as time-drawdown curves and include effects of storage in the aquitard, unconfined conditions, partially penetrating wells and stratified aquifers. The outcome of calculations for relatively simple systems compares very well with published corresponding results. The proposed multilayer solution can be a valuable tool in aquifer test evaluation, as it provides the analytical expression required to enable the application of existing computer methods to the determination of aquifer characteristics.

Analysis of data from test-well sites along the downdip limit of freshwater in the Edwards Aquifer, San Antonio, Texas, 1985-87

Science.gov (United States)

Groschen, G.E.

1994-01-01

Many researchers have studied the downdip limit of freshwater in the Edwards aquifer or various aspects of the saline-water zone and its relation to the freshwater zone. These studies were summarized and used to synthesize a consistent hydrologic and geochemical framework from which to interpret data from field studies. The concept derived from the previous work on the downdip limit of the freshwater zone is that fresh recharge water entered the aquifer and developed a vast flow system controlled by barrier faults. Some recharge water flows into the saline-water zone rather than toward major freshwater discharge points. The water that enters the salinewater zone continues to dissolve gypsum and dolomite, and calcite precipitates out of the water. This process of dedolomitization has helped to develop the large secondary porosity of the freshwater zone as the downdip limit of the freshwater zone progressively moved downdip in recent geologic time.

Guarani aquifer hydrogeological synthesis of the Guarani aquifer system. Edicion bilingue

International Nuclear Information System (INIS)

2009-01-01

This work represents the synthesis of current knowledge of the Guarani Aquifer System, based on technical products made by different companies and consultants who participated in the framework of the Project for Environmental Protection and Sustainable Development of the Guarani Aquifer.

Monitoring Aquifer Depletion from Space: Case Studies from the Saharan and Arabian Aquifers

Science.gov (United States)

Ahmed, M.; Sultan, M.; Wahr, J. M.; Yan, E.

2013-12-01

Access to potable fresh water resources is a human right and a basic requirement for economic development in any society. In arid and semi-arid areas, the characterization and understanding of the geologic and hydrologic settings of, and the controlling factors affecting, these resources is gaining increasing importance due to the challenges posed by increasing population. In these areas, there is immense natural fossil fresh water resources stored in large extensive aquifers, the transboundary aquifers. Yet, natural phenomena (e.g., rainfall patterns and climate change) together with human-related factors (e.g., population growth, unsustainable over-exploitation, and pollution) are threatening the sustainability of these resources. In this study, we are developing and applying an integrated cost-effective approach to investigate the nature (i.e., natural and anthropogenic) and the controlling factors affecting the hydrologic settings of the Saharan (i.e., Nubian Sandstone Aquifer System [NSAS], Northwest Sahara Aquifer System [NWSA]) and Arabian (i.e., Arabian Peninsula Aquifer System [APAS]) aquifer systems. Analysis of the Gravity Recovery and Climate Experiment (GRACE)-derived Terrestrial Water Storage (TWS) inter-annual trends over the NSAS and the APAS revealed two areas of significant TWS depletions; the first correlated with the Dakhla Aquifer System (DAS) in the NSAS and second with the Saq Aquifer System (SAS) in the APAS. Annual depletion rates were estimated at 1.3 × 0.66 × 109 m3/yr and 6.95 × 0.68 × 109 m3/yr for DAS and SAS, respectively. Findings include (1) excessive groundwater extraction, not climatic changes, is responsible for the observed TWS depletions ;(2) the DAS could be consumed in 350 years if extraction rates continue to double every 50 years and the APAS available reserves could be consumed within 60-140 years at present extraction (7.08 × 109 m3/yr) and depletion rates; and (3) observed depletions over DAS and SAS and their

Field demonstration of CO2 leakage detection in potable aquifers with a pulselike CO2-release test.

Science.gov (United States)

Yang, Changbing; Hovorka, Susan D; Delgado-Alonso, Jesus; Mickler, Patrick J; Treviño, Ramón H; Phillips, Straun

2014-12-02

This study presents two field pulselike CO2-release tests to demonstrate CO2 leakage detection in a shallow aquifer by monitoring groundwater pH, alkalinity, and dissolved inorganic carbon (DIC) using the periodic groundwater sampling method and a fiber-optic CO2 sensor for real-time in situ monitoring of dissolved CO2 in groundwater. Measurements of groundwater pH, alkalinity, DIC, and dissolved CO2 clearly deviated from their background values, showing responses to CO2 leakage. Dissolved CO2 observed in the tests was highly sensitive in comparison to groundwater pH, DIC, and alkalinity. Comparison of the pulselike CO2-release tests to other field tests suggests that pulselike CO2-release tests can provide reliable assessment of geochemical parameters indicative of CO2 leakage. Measurements by the fiber-optic CO2 sensor, showing obvious leakage signals, demonstrated the potential of real-time in situ monitoring of dissolved CO2 for leakage detection at a geologic carbon sequestration (GCS) site. Results of a two-dimensional reactive transport model reproduced the geochemical measurements and confirmed that the decrease in groundwater pH and the increases in DIC and dissolved CO2 observed in the pulselike CO2-release tests were caused by dissolution of CO2 whereas alkalinity was likely affected by carbonate dissolution.

Source, variability, and transformation of nitrate in a regional karst aquifer: Edwards aquifer, central Texas.

Science.gov (United States)

Musgrove, MaryLynn; Opsahl, Stephen P.; Mahler, Barbara J.; Herrington, Chris; Sample, Thomas; Banta, John

2016-01-01

Many karst regions are undergoing rapid population growth and expansion of urban land accompanied by increases in wastewater generation and changing patterns of nitrate (NO3−) loading to surface and groundwater. We investigate variability and sources of NO3− in a regional karst aquifer system, the Edwards aquifer of central Texas. Samples from streams recharging the aquifer, groundwater wells, and springs were collected during 2008–12 from the Barton Springs and San Antonio segments of the Edwards aquifer and analyzed for nitrogen (N) species concentrations and NO3− stable isotopes (δ15N and δ18O). These data were augmented by historical data collected from 1937 to 2007. NO3− concentrations and discharge data indicate that short-term variability (days to months) in groundwater NO3− concentrations in the Barton Springs segment is controlled by occurrence of individual storms and multi-annual wet-dry cycles, whereas the lack of short-term variability in groundwater in the San Antonio segment indicates the dominance of transport along regional flow paths. In both segments, longer-term increases (years to decades) in NO3− concentrations cannot be attributed to hydrologic conditions; rather, isotopic ratios and land-use change indicate that septic systems and land application of treated wastewater might be the source of increased loading of NO3−. These results highlight the vulnerability of karst aquifers to NO3− contamination from urban wastewater. An analysis of N-species loading in recharge and discharge for the Barton Springs segment during 2008–10 indicates an overall mass balance in total N, but recharge contains higher concentrations of organic N and lower concentrations of NO3−than does discharge, consistent with nitrification of organic N within the aquifer and consumption of dissolved oxygen. This study demonstrates that subaqueous nitrification of organic N in the aquifer, as opposed to in soils, might be a previously

Statistical interpretation of geochemical data

International Nuclear Information System (INIS)

Carambula, M.

1990-01-01

Statistical results have been obtained from a geochemical research from the following four aerial photographies Zapican, Carape, Las Canias, Alferez. They have been studied 3020 samples in total, to 22 chemical elements using plasma emission spectrometry methods.

Uruguay mining inventory. Geochemical prospecting results of the Las Flores aerial map

International Nuclear Information System (INIS)

Zeegers, H.; Bonnefoy, D.; Garau, M.; Spangenberg, J.

1981-01-01

In the context of the Uruguay mining inventory, the aerial photography map Las Flores had been covered by a specific strategic which included geochemical prospecting elements. The surface covered has the 550 km2, and 1042 samples which they have been analized in Orleans France. 22 elements by plasma spectroscopy and gold by atomic absorption and for uranium laser spectroscopy . They have been evidenced the following anomalies: gold, Pb, Pb-Ba-Cu, Ba and Ni-Cr

Integrated geophysical-geochemical methods for archaeological prospecting

OpenAIRE

Persson, Kjell

2005-01-01

A great number of field measurements with different methods and instruments were conducted in attempts to develop a method for an optimal combination of various geochemical and geophysical methods in archaeological prospecting. The research presented in this thesis focuses on a study of how different anthropogenic changes in the ground can be detected by geochemical and geophysical mapping and how the results can be presented. A six-year pilot project, Svealand in Vendel and Viking periods (S...

Groundwater vulnerability mapping of Qatar aquifers

Science.gov (United States)

Baalousha, Husam Musa

2016-12-01

Qatar is one of the most arid countries in the world with limited water resources. With little rainfall and no surface water, groundwater is the only natural source of fresh water in the country. Whilst the country relies mainly on desalination of seawater to secure water supply, groundwater has extensively been used for irrigation over the last three decades, which caused adverse environmental impact. Vulnerability assessment is a widely used tool for groundwater protection and land-use management. Aquifers in Qatar are carbonate with lots of fractures, depressions and cavities. Karst aquifers are generally more vulnerable to contamination than other aquifers as any anthropogenic-sourced contaminant, especially above a highly fractured zone, can infiltrate quickly into the aquifer and spread over a wide area. The vulnerability assessment method presented in this study is based on two approaches: DRASTIC and EPIK, within the framework of Geographical Information System (GIS). Results of this study show that DRASTIC vulnerability method suits Qatar hydrogeological settings more than EPIK. The produced vulnerability map using DRASTIC shows coastal and karst areas have the highest vulnerability class. The southern part of the country is located in the low vulnerability class due to occurrence of shale formation within aquifer media, which averts downward movement of contaminants.

Coastal groundwater salinization: Focus on the vertical variability in a multi-layered aquifer through a multi-isotope fingerprinting (Roussillon Basin, France)

Energy Technology Data Exchange (ETDEWEB)

Petelet-Giraud, Emmanuelle, E-mail: e.petelet@brgm.fr [BRGM, Avenue C. Guillemin, BP 36009, 45060 Orléans Cedex 02 (France); Négrel, Philippe [BRGM, Avenue C. Guillemin, BP 36009, 45060 Orléans Cedex 02 (France); Aunay, Bertrand [BRGM, Réunion Agency, 5, rue Sainte-Anne, CS 51016, 97404 Saint Denis Cedex (France); Ladouche, Bernard; Bailly-Comte, Vincent [BRGM Montpellier Agency, 1039, rue de Pinville, 34000 Montpellier (France); Guerrot, Catherine; Flehoc, Christine [BRGM, Avenue C. Guillemin, BP 36009, 45060 Orléans Cedex 02 (France); Pezard, Philippe; Lofi, Johanna [Géosciences Montpellier, UMR 5243, Université de Montpellier, cc069, Place Eugène Bataillon, 34095 Montpellier Cedex 05 (France); Dörfliger, Nathalie [BRGM, Avenue C. Guillemin, BP 36009, 45060 Orléans Cedex 02 (France)

2016-10-01

The Roussillon sedimentary Basin (South France) is a complex multi-layered aquifer, close to the Mediterranean Sea facing seasonally increases of water abstraction and salinization issues. We report geochemical and isotopic vertical variability in this aquifer using groundwater sampled with a Westbay System® at two coastal monitoring sites: Barcarès and Canet. The Westbay sampling allows pointing out and explaining the variation of water quality along vertical profiles, both in productive layers and in the less permeable ones where most of the chemical processes are susceptible to take place. The aquifer layers are not equally impacted by salinization, with electrical conductivity ranging from 460 to 43,000 μS·cm{sup −1}. The δ{sup 2}H–δ{sup 18}O signatures show mixing between seawater and freshwater components with long water residence time as evidenced by the lack of contribution from modern water using {sup 3}H, {sup 14}C and CFCs/SF6. S(SO{sub 4}) isotopes also evidence seawater contribution but some signatures can be related to oxidation of pyrite and/or organically bounded S. In the upper layers {sup 87}Sr/{sup 86}Sr ratios are close to that of seawater and then increase with depth, reflecting water–rock interaction with argillaceous formations while punctual low values reflect interaction with carbonate. Boron isotopes highlight secondary processes such as adsorption/desorption onto clays in addition to mixings. At the Barcarès site (120 m deep), the high salinity in some layers appear to be related neither to present day seawater intrusion, nor to Salses-Leucate lagoonwater intrusion. Groundwater chemical composition thus highlights binary mixing between fresh groundwater and inherited salty water together with cation exchange processes, water–rock interactions and, locally, sedimentary organic matter mineralisation probably enhanced by pyrite oxidation. Finally, combining the results of this study and those of Caballero and Ladouche (2015

Relation between "terra rossa" from the Apulia aquifer of Italy and the radon content of groundwater: Experimental results and their applicability to radon occurrence in the aquifer

Science.gov (United States)

Tadolini, T.; Spizzico, M.

The radon-222 (222Rn) activity in groundwater of the Apulian karstic aquifer in southern Italy is as great as 500 Becquerel per liter (Bq/L) locally. Normal radium-226 (226Ra) activity in the limestone and calcareous dolomites of the aquifer is not enough to explain such a high level. Laboratory investigations identified high 226Ra activity in the "terra rossa," the residuum occupying fissures and cavities in the bedrock, and also the relation between (1) 226Ra-bearing bedrock and "terra rossa" and (2) 222Rn in water. The "terra rossa" is the primary source of the radon in the groundwater. The experimental results show the need to characterize the "terra rossa" of Apulia on the basis of 226Ra activity and also to study the distribution and variations in 222Rn activity over time in the aquifer. Résumé L'activité du radon-222 (222Rn) dans les eaux souterraines de l'aquifère karstique des Pouilles, dans le sud de l'Italie, atteint localement 500 Becquerel par litre (Bq/L). L'activité normale du radium-226 (226Ra) dans les calcaires et dans les calcaires dolomitiques de l'aquifère n'est pas assez élevée pour expliquer des valeurs aussi élevées. Des analyses de laboratoire ont mis en évidence une forte activité en 226Ra dans la terra rossa, remplissage de fissures et de cavités de la roche, ainsi qu'une relation entre (1) la roche et la terra rossa contenant du 226Ra et (2) le 222Rn dans l'eau. La terra rossa est la source primaire de radon dans l'eau souterraine. Les résultats expérimentaux montrent qu'il est nécessaire de caractériser la terra rossa des Pouilles par son activité en 226Ra et d'étudier la distribution et les variations de l'activité en 222Rn au cours du temps dans l'aquifère. Resumen La actividad del radon-222 (222Rn) en el agua subterránea del acuífero cárstico de Apulia, al sur de Italia, alcanza localmente los 500Bq/L. La actividad normal del radio-226 (226Ra) en las calcitas y dolomitas del acuífero no es suficiente para

Hydrochemical processes in a shallow coal seam gas aquifer and its overlying stream–alluvial system: implications for recharge and inter-aquifer connectivity

International Nuclear Information System (INIS)

Duvert, Clément; Raiber, Matthias; Owen, Daniel D.R.; Cendón, Dioni I.; Batiot-Guilhe, Christelle; Cox, Malcolm E.

2015-01-01

margins. Most waters collected from the coal-bearing aquifer also showed an enhanced influence of weathering during the wet season, which was likely triggered by the water–rock interaction with fresh recharge waters. An increase in both residual alkalinity and carbon isotopic ratios at two locations indicated inter-aquifer mixing between alluvium and bedrock during the wet season. The results of this study emphasise the need for conducting baseline hydrochemical surveys prior to CSG development in order to describe the transient nature of recharge and inter-aquifer mixing processes

Potential for a process-based monitoring method above geologic carbon storage sites using dissolved gases in freshwater aquifers

Energy Technology Data Exchange (ETDEWEB)

Romanak, Katherine [Gulf Coast Carbon Center, Bureau of Economic Geology, The University of Texas at Austin, TX 78713 (United States); Dobeck, Laura; Spangler, Lee [Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT 59717 (United States); Dixon, Tim [IEA Greenhouse Gas R and D Programme, Cheltenham GL52 7RZ (United Kingdom)

2013-07-01

The process-based method is a new technique for monitoring CO{sub 2} storage permanence in the vadose zone above geologic carbon storage (GCS) sites. This method uses ratios of coexisting gas species to understand geochemical processes rather than comparing CO{sub 2} concentrations with large baseline data sets, thereby making monitoring more efficient. In the vadose zone, ratios among coexisting gases (CO{sub 2}, O{sub 2}, N{sub 2} and CH{sub 4}) have been used to distinguish biologic respiration, water-rock-CO{sub 2} interaction, and methane oxidation from a leakage signal. We report the preliminary results of a feasibility test conducted in July 2012 at the Zero Emission Research and Technology Center (ZERT) controlled release site in Montana, USA to discern whether the method could be applied to dissolved gases in groundwater, thereby enhancing groundwater monitoring. Preliminary results are favorable, making the process-based approach potentially useful for monitoring shallow freshwater aquifers above GCS sites. (authors)

Hydrogeochemistry of regional aquifer systems from Tuscany (central Italy): the state of the art before the definition of a geochemical baseline

Science.gov (United States)

Nisi, Barbara; Battaglini, Raffaele; Raco, Brunella

2013-04-01

European Community Water Framework Directive (WFD) and its derivative regulations have recognized the urgent need to adopt specific measures against the contamination of water bodies by individual pollutants that may significantly affect the quality of water itself. Italian regulation takes into account the EU Directives, and charges the regional authorities to create monitoring networks and produce assessment reports on the contamination of groundwater. The knowledge of "natural baseline" for various dissolved elements in groundwaters on a regional scale becomes of primary importance to distinguish natural sources and anthropogenic inputs. The studied area includes the whole Tuscan regional district (central Italy) and covers an area of about 23,000 km2. From a geolithological point of view, Tuscan territory consists of several complexes outcropping regionally, the most typical features being the Mesozoic and Cenozoic carbonate and evaporitic formations, overlain by flysch sequences, as well as granite intrusions and volcanic rocks. Moreover, two geothermal areas (Larderello and Mt. Amiata), a large number of thermal springs and CO2-rich gas vents are mostly present in the central-southern part of Tuscany. Finally in southern Tuscany (e.g. Campiglia M.Ma, Mt. Amiata, Elba Island), mining districts, predominantly characterized by polimetallic sulphides ore deposits, were exploited since the Etruscan time. In this work statistical distribution models are used to develop summary statistics and estimate probabilities of exceeding water-quality standards according to the National Legislative Decree 152/06. Descriptive statistics on solute concentrations are based on geochemical data from the main Tuscan aquifers and investigated by the CNR-IGG (Institute of Geosciences and Earth Resources of Pisa, Italy) and Department of Earth Sciences (University of Florence, Italy). The data processing was carried out on 4,767 water samples collected from 1997 to 2009. According to

Hydrogeology and geochemistry of aquifers underlying the San Lorenzo and San Leandro areas of the East Bay Plain, Alameda County, California

Science.gov (United States)

Izbicki, John A.; Borchers, James W.; Leighton, David A.; Kulongoski, Justin T.; Fields, Latoya; Galloway, Devin L.; Michel, Robert L.

2003-01-01

The East Bay Plain, on the densely populated eastern shore of San Francisco Bay, contains an upper aquifer system to depths of 250 feet below land surface and an underlying lower aquifer system to depths of more than 650 feet. Injection and recovery of imported water has been proposed for deep aquifers at two sites within the lower aquifer system. Successful operation requires that the injected water be isolated from surface sources of poor-quality water during storage and recovery. Hydraulic, geochemical, and isotopic data were used to evaluate the isolation of deeper aquifers. Ground-water responses to tidal changes in the Bay suggest that thick clay layers present within these deposits effectively isolate the deeper aquifers in the northern part of the study area from overlying surficial deposits. These data also suggest that the areal extent of the shallow and deep aquifers beneath the Bay may be limited in the northern part of the study area. Despite its apparent hydraulic isolation, the lower aquifer system may be connected to the overlying upper aquifer system through the corroded and failed casings of abandoned wells. Water-level measurements in observation wells and downward flow measured in selected wells during nonpumped conditions suggest that water may flow through wells from the upper aquifer system into the lower aquifer system during nonpumped conditions. The chemistry of water from wells in the East Bay Plain ranges from fresh to saline; salinity is greater than seawater in shallow estuarine deposits near the Bay. Water from wells completed in the lower aquifer system has higher pH, higher sodium, chloride, and manganese concentrations, and lower calcium concentrations and alkalinity than does water from wells completed in the overlying upper aquifer system. Ground-water recharge temperatures derived from noble-gas data indicate that highly focused recharge processes from infiltration of winter streamflow and more diffuse recharge processes from

Maps of estimated nitrate and arsenic concentrations in basin-fill aquifers of the southwestern United States

Science.gov (United States)

Beisner, Kimberly R.; Anning, David W.; Paul, Angela P.; McKinney, Tim S.; Huntington, Jena M.; Bexfield, Laura M.; Thiros, Susan A.

2012-01-01

Human-health concerns and economic considerations associated with meeting drinking-water standards motivated a study of the vulnerability of basin-fill aquifers to nitrate contamination and arsenic enrichment in the southwestern United States. Statistical models were developed by using the random forest classifier algorithm to predict concentrations of nitrate and arsenic across a model grid representing about 190,600 square miles of basin-fill aquifers in parts of Arizona, California, Colorado, Nevada, New Mexico, and Utah. The statistical models, referred to as classifiers, reflect natural and human-related factors that affect aquifer vulnerability to contamination and relate nitrate and arsenic concentrations to explanatory variables representing local- and basin-scale measures of source and aquifer susceptibility conditions. Geochemical variables were not used in concentration predictions because they were not available for the entire study area. The models were calibrated to assess model accuracy on the basis of measured values.Only 2 percent of the area underlain by basin-fill aquifers in the study area was predicted to equal or exceed the U.S. Environmental Protection Agency drinking-water standard for nitrate as N (10 milligrams per liter), whereas 43 percent of the area was predicted to equal or exceed the standard for arsenic (10 micrograms per liter). Areas predicted to equal or exceed the drinking-water standard for nitrate include basins in central Arizona near Phoenix; the San Joaquin Valley, the Santa Ana Inland, and San Jacinto Basins of California; and the San Luis Valley of Colorado. Much of the area predicted to equal or exceed the drinking-water standard for arsenic is within a belt of basins along the western portion of the Basin and Range Physiographic Province that includes almost all of Nevada and parts of California and Arizona. Predicted nitrate and arsenic concentrations are substantially lower than the drinking-water standards in much of

Carboniferous Granitoid Magmatism of Northern Taimyr: Results of Isotopic-Geochemical Study and Geodynamic Interpretation

Science.gov (United States)

Kurapov, M. Yu.; Ershova, V. B.; Makariev, A. A.; Makarieva, E. V.; Khudoley, A. K.; Luchitskaya, M. V.; Prokopiev, A. V.

2018-03-01

Data on the petrography, geochemistry, and isotopic geochronology of granites from the northern part of the Taimyr Peninsula are considered. The Early-Middle Carboniferous age of these rocks has been established (U-Pb, SIMS). Judging by the results of 40Ar/39Ar dating, the rocks underwent metamorphism in the Middle Permian. In geochemical and isotopic composition, the granitic rocks have much in common with evolved I-type granites. This makes it possible to specify a suprasubduction marginal continental formation setting. The existence of an active Carboniferous margin along the southern edge of the Kara Block (in presentday coordinates) corroborates the close relationship of the studied region with the continent of Baltia.

Nutrient Removal during Stormwater Aquifer Storage and Recovery in an Anoxic Carbonate Aquifer.

Science.gov (United States)

Vanderzalm, Joanne L; Page, Declan W; Dillon, Peter J; Barry, Karen E; Gonzalez, Dennis

2018-03-01

Stormwater harvesting coupled to managed aquifer recharge (MAR) provides a means to use the often wasted stormwater resource while also providing protection of the natural and built environment. Aquifers can act as a treatment barrier within a multiple-barrier approach to harvest and use urban stormwater. However, it remains challenging to assess the treatment performance of a MAR scheme due to the heterogeneity of aquifers and MAR operations, which in turn influences water treatment processes. This study uses a probabilistic method to evaluate aquifer treatment performance based on the removal of total organic C (TOC), N, and P during MAR with urban stormwater in an anoxic carbonate aquifer. Total organic C, N, and P are represented as stochastic variables and described by probability density functions (PDFs) for the "injectant" and "recovery"; these injectant and recovery PDFs are used to derive a theoretical MAR removal efficiency PDF. Four long-term MAR sites targeting one of two tertiary carbonate aquifers (T1 and T2) were used to describe the nutrient removal efficiencies. Removal of TOC and total N (TN) was dominated by redox processes, with median removal of TOC between 50 and 60% at all sites and TN from 40 to 50% at three sites with no change at the fourth. Total P removal due to filtration and sorption accounted for median removal of 29 to 53%. Thus, the statistical method was able to characterize the capacity of the anoxic carbonate aquifer treatment barrier for nutrient removal, which highlights that aquifers can be an effective long-term natural treatment option for management of water quality, as well as storage of urban stormwater. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Managed Aquifer Recharge Using Treated Wastewater: An Option to Manage a Coastal Aquifer In Oman For Better Domestic Water Supply

Science.gov (United States)

Al-Maktoumi, Ali; Zekri, Slim; ElRawy, Mustafa

2016-04-01

Arid countries, such as the Sultanate of Oman, are facing challenges of water shortages threatening economic development and social stability. Most of those countries are vulnerable to the potential adverse impacts of climate change, the most significant of which are increased average temperatures, less and more erratic precipitation, sea level rise, and desertification. The combined effect of existing adverse conditions and likely impacts of future climate change will make water management even more difficult than what it is today. Tremendous efforts have been devoted to augment the water resources. Managed Aquifer Recharge (MAR) is practiced widely to store water during periods of surpluses and withdraw during deficits from an aquifer. In Muscat, there will be a surplus of >100,000 m3/day of TWW during winter months in the coming few years. The aquifer along the northern coast of Oman (Al-Khawd Aquifer) is conducive for MAR. Data show that TWW volumes will increase from 7.6 Mm3 in 2003 to 70.9 Mm3 in 2035 in Muscat city only. This study assesses, using MODFLOW 2005 numerical code, the impact of MAR using TWW on better management of the Al-Khawd unconfined coastal aquifer for better urban water supply. Specifically, aiming to maximize withdrawals from the domestic wells with minimize adverse effect of seawater intrusion. The model operates under a number of constrains that minimize the loss to the sea and the injected TWW must not migrates upstream (due to developed mound) and reach the wellfields used for domestic supply. The hypothetical injection wells are located downstream the domestic wellfield zone. The results of different managerial scenarios show that MAR produces a hydraulic barrier that decelerates the seawater intrusion which allows higher abstraction of pristine water from the upstream part of the aquifer. MAR along with redistribution/relocation of public wells allows abstraction of 2 times the current abstraction rate (around 6 Mm3/year to 12 Mm3

Regeneration of a confined aquifer after redevelopment and decommission of artesian wells, example from Grafendorf aquifer (Styria, Austria)

Science.gov (United States)

Mehmedovski, Nudzejma; Winkler, Gerfried

2016-04-01

Water is essential for life and it is therefore necessary to protect drinking water sustainably. Compared to shallow groundwater, deeper groundwater is especially important due to its characteristic tendency to remain extensively unaffected by environmental impacts. Thus, the uncontrolled waste of this valuable resource has to be avoided. A lot of artesian wells have been established in Grafendorf bei Hartberg (Styria, Austria). Almost all wells were not state-of-the art. As a result the different aquifer horizons began to intermix. Additionally some of the artesian wells had a permanent free overflow and the water was not even used. Consequently, since 1950, where the mean discharge of 37 wells was 0,334 l/s per well, the discharge has decreased to 0,090 l/s until 2013, which means a decline of about 75 %. As a reaction to these declines a decommissioning campaign was conducted where 69 artesian wells have been closed by injecting a cement-bentonite suspension (ratio 3:1). The Grafendorf aquifer is situated in the Styrian Basin and consists of 5 separated artesian horizons in Neogene sediments. These artesian horizons range from 42 m (1st horizon) to 176 m (5th horizon) and mostly consist of sand, partly of fine/medium/coarse gravel and partially with minor clay content. In order to analyse the reaction of the Grafendorf aquifer to these redevelopments, 5 monitoring wells could be used for the analysis. Some monitoring wells include different aquifer horizons and hydraulically short cut them. Thus, in this work the analysis focus on the general trend of the whole aquifer system neglecting the individual interactions between the different aquifers. In a first investigation step the hydraulic properties of the aquifer system has been determined using pumping tests which were analysed with different analytical solutions with the software AQTESOLV. Overall the pumping test solutions hardly differ in the transmissivity and hydraulic conductivity. On the contrary the

Saltwater intrusion in the surficial aquifer system of the Big Cypress Basin, southwest Florida, and a proposed plan for improved salinity monitoring

Science.gov (United States)

Prinos, Scott T.

2013-01-01

The installation of drainage canals, poorly cased wells, and water-supply withdrawals have led to saltwater intrusion in the primary water-use aquifers in southwest Florida. Increasing population and water use have exacerbated this problem. Installation of water-control structures, well-plugging projects, and regulation of water use have slowed saltwater intrusion, but the chloride concentration of samples from some of the monitoring wells in this area indicates that saltwater intrusion continues to occur. In addition, rising sea level could increase the rate and extent of saltwater intrusion. The existing saltwater intrusion monitoring network was examined and found to lack the necessary organization, spatial distribution, and design to properly evaluate saltwater intrusion. The most recent hydrogeologic framework of southwest Florida indicates that some wells may be open to multiple aquifers or have an incorrect aquifer designation. Some of the sampling methods being used could result in poor-quality data. Some older wells are badly corroded, obstructed, or damaged and may not yield useable samples. Saltwater in some of the canals is in close proximity to coastal well fields. In some instances, saltwater occasionally occurs upstream from coastal salinity control structures. These factors lead to an incomplete understanding of the extent and threat of saltwater intrusion in southwest Florida. A proposed plan to improve the saltwater intrusion monitoring network in the South Florida Water Management District’s Big Cypress Basin describes improvements in (1) network management, (2) quality assurance, (3) documentation, (4) training, and (5) data accessibility. The plan describes improvements to hydrostratigraphic and geospatial network coverage that can be accomplished using additional monitoring, surface geophysical surveys, and borehole geophysical logging. Sampling methods and improvements to monitoring well design are described in detail. Geochemical analyses

Ground-water flow directions and estimation of aquifer hydraulic properties in the lower Great Miami River Buried Valley aquifer system, Hamilton Area, Ohio

Science.gov (United States)

Sheets, Rodney A.; Bossenbroek, Karen E.

2005-01-01

The Great Miami River Buried Valley Aquifer System is one of the most productive sources of potable water in the Midwest, yielding as much as 3,000 gallons per minute to wells. Many water-supply wells tapping this aquifer system are purposely placed near rivers to take advantage of induced infiltration from the rivers. The City of Hamilton's North Well Field consists of 10 wells near the Great Miami River, all completed in the lower Great Miami River Buried Valley Aquifer System. A well-drilling program and a multiple-well aquifer test were done to investigate ground-water flow directions and to estimate aquifer hydraulic properties in the lower part of the Great Miami River Buried Valley Aquifer System. Descriptions of lithology from 10 well borings indicate varying amounts and thickness of clay or till, and therefore, varying levels of potential aquifer confinement. Borings also indicate that the aquifer properties can change dramatically over relatively short distances. Grain-size analyses indicate an average bulk hydraulic conductivity value of aquifer materials of 240 feet per day; the geometric mean of hydraulic conductivity values of aquifer material was 89 feet per day. Median grain sizes of aquifer material and clay units were 1.3 millimeters and 0.1 millimeters, respectively. Water levels in the Hamilton North Well Field are affected by stream stage in the Great Miami River and barometric pressure. Bank storage in response to stream stage is evident. Results from a multiple-well aquifer test at the well field indicate, as do the lithologic descriptions, that the aquifer is semiconfined in some areas and unconfined in others. Transmissivity and storage coefficient of the semiconfined part of the aquifer were 50,000 feet squared per day and 5x10-4, respectively. The average hydraulic conductivity (450 feet per day) based on the aquifer test is reasonable for glacial outwash but is higher than calculated from grain-size analyses, implying a scale effect

Modelling the transfer of chemical pollutants to the aquifer in the very low level waste disposal site of El Cabril, Spain

International Nuclear Information System (INIS)

Duro, L.; Merino, J.; Grive, M.; Jordana, S.; Bruno, J.; Ordonez, M.

2005-01-01

A Very Low Level Radioactive Waste disposal site is being planned in El Cabril, Spain, where a Low and Intermediate Level Radioactive Waste disposal site is already located. As part of the ongoing safety assessment for this new facility, we have modelled the transfer of chemical pollutants from the disposal site to the underlying aquifer. The conceptual model is based on the water transport due to the infiltration of rain through the disposal cell. The source term is given by the dissolution of the initial inventory limited by sorption in cement (the main form of the waste) and secondary phase solubility. Several assumptions have been made: all protective layers are degraded, the system is saturated and the water flux is stationary and unidimensional in the vertical direction. A compartment modelling approach has been followed, and the system has been divided in four compartments: Top clay layer, Waste, Bottom clay layer and Subsoil. The latter acts as a sink representing the discharge to the aquifer. Advective and diffusive fluxes are defined between the compartments taking into account hydrological, geochemical and transport properties of the different materials and compounds. The results of the simulation (up to 106 years) show that there is an initial increase in the contaminant release to the aquifer due to the leaching of the waste by the infiltrating waters until a maximum is obtained. In most of the elements the maximum is given by their respective solubility limit and therefore the release is constant during all the time the concentration in the pore water is controlled by solubility. (author)

Geochemical behaviour of natural uranium-series nuclides in geological formation

International Nuclear Information System (INIS)

Yamakawa, Minoru

1991-01-01

Recent research and investigation show that the Tono uranium deposit and its natural uranium-series nuclides have been preserved, without any significant changes like re-migration or reconcentration, throughout geological events such as upheaval-submergence, marine transgression-regression, and faulting which can readily change geological, hydrogeological, and geochemical conditions. This situation might have come about as a result of being kept in a geometrical closure system, with reducing and milk alkalic geochemical conditions, from the hydrogeological and geochemical point of view. (author)

Geochemical mapping study of Panjang island

International Nuclear Information System (INIS)

Sutisna; Sumardjo

2010-01-01

Impact of industrial and regional development are not only related to an improvement of socio-economic, but also to an environmental conservation and sustainable. This impact could be observed on a change of geochemical mapping before and after an operational of the industry. In the relation with a regional development and resources utilization, the geochemical mapping have been done in the aim to know a resources and an elemental distribution at Panjang island. In this research, ko-Instrumental Neutron Activation Analysis (k_0-INAA) have been applied in an elemental quantification on the geochemical mapping. Pencuplikan of geochemical sample have been carried out by using a grid systematic method with a sample density of about 10 sample per square kilometre involved 85 pencuplikan point. The geochemical sample of sediment and soil have been provided as a dry weight of 100 mesh. Internal quality control have done by using a number of Standard Reference Materials obtained from US. Geological Survey. Fifteen elements of Sc, Co, In, Rb, Mo, Ba, Ce, Nd, Eu, La, Yb, Th, U, lr and Hf contained in standard materials have been evaluated. The analysis result show that a relative standard deviation less than 11 %, except for Mo (13 %) and lr (26 %). Fourteen elements of Al, Br, Ca, Co, Eu, Fe, La, U, Na, Ce, Mn, As, Sc and Th have been mapped and presented in this paper. The major elements of Ca, Al and Fe, and minor elements of Mn, U and Sc are distributed at all region. The lanthanide elements of La, Ce and Eu have vary concentration and could be found at the middle to the north of the island. (author)

Geochemical behavior of uranium mill tailings leachate in the subsurface

International Nuclear Information System (INIS)

Brookins, D.G.

1993-01-01

Leachate generated from surface disposal of acidic uranium mill tailings at Maybell, CO has impacted groundwater quality within the underlying mineralized Browns Park Formation. The extent of groundwater contamination, however, is located directly beneath the tailings impoundment. The milling process consisted of sulfuric acid extraction of uranium from the feed ore by a complex chemical leaching and precipitation process. Tailings leachate at the site contains elevated concentrations of Al, As, Cd, Mo, Ni, NO 3 , Se, U, and other solutes. From column leach tests, the concentrations of contaminants within tailings pore fluid are SO 4 >NH 4 >NO 3 >U>Se>Ni>As>Cd at pH 4.0. The carbonate buffering capacity of the tailings subsoil has decreased because of calcite dissolution in the presence of acidic leachate. Groundwater quality data, mineralogical and microbiological studies, and geochemical modeling suggest that As, NO 3 , Se, U and other solutes are being removed from solution through precipitation, adsorption, and denitrification processes under reducing conditions. Presence of hydrogen sulfide, liquid and gaseous hydrocarbons, dissolved organic, and abundant pyrite within the Browns Park Formations have maintained reducing conditions subjacent to the tailings impoundment. Groundwater is in close equilibrium with coffinite and uraninite, the primary U(IV) minerals extracted from the Browns Parks Formation. Denitrifying bacteria identified in this study catalyze redox reactions involving NO 3 . Subsequently, contaminant distributions of NO 3 decrease 1000 times beneath the tailings impoundment. Applying geochemical and biochemical processes occurring at Maybell provides an excellent model for in situ aquifer restoration programs considered at other uranium tailings and heavy-metal-mixed waste contaminated sites. (author) 4 figs., 4 tabs., 27 refs

Identifying Stream/Aquifer Exchange by Temperature Gradient in a Guarani Aquifer System Outcrop Zone

Science.gov (United States)

Wendland, E.; Rosa, D. M. S.; Anache, J. A. A.; Lowry, C.; Lin, Y. F. F.

2017-12-01

Recharge of the Guarani Aquifer System (GAS) in South America is supposed to occur mainly in the outcrop zones, where the GAS appears as an unconfined aquifer (10% of the 1.2 Million km2 aquifer extension). Previous evaluations of recharge are based essentially on water balance estimates for the whole aquifer area or water table fluctuations in monitoring wells. To gain a more detailed understanding of the recharge mechanisms the present work aimed to study the stream aquifer interaction in a watershed (Ribeirão da Onça) at an outcrop zone. Two Parshall flumes were installed 1.3 km apart for discharge measurement in the stream. Along this distance an optic fiber cable was deployed to identify stretches with gaining and losing behavior. In order to estimate groundwater discharge in specific locations, 8 temperature sticks were set up along the stream reach to measure continuously the vertical temperature gradient. A temperature probe with 4 thermistors was also used to map the shallow streambed temperature gradient manually along the whole distance. The obtained results show a discharge difference of 250 m3/h between both flumes. Since the last significant rainfall (15 mm) in the watershed occurred 3 months ago, this value can be interpreted as the base flow contribution to the stream during the dry season. Given the temperature difference between groundwater ( 24oC) and surface water ( 17oC) the fiber-optic distributed temperature sensing (FO-DTS) allowed the identification of stretches with gaining behavior. Temperature gradients observed at the streambed varied between 0.67 and 14.33 oC/m. The study demonstrated that heat may be used as natural tracer even in tropical conditions, where the groundwater temperature is higher than the surface water temperature during the winter. The obtained results show that the discharge difference between both flumes can not be extrapolated without detailed analysis. Gaining and loosing stretches have to be identified on order

A convenient method for estimating the contaminated zone of a subsurface aquifer resulting from radioactive waste disposal into ground

International Nuclear Information System (INIS)

Fukui, Masami; Katsurayama, Kousuke; Uchida, Shigeo.

1981-01-01

Studies were conducted to estimate the contamination spread resulting from the radioactive waste disposal into a subsurface aquifer. A general equation, expressing the contaminated zone as a function of radioactive decay, the physical and chemical parameters of soil is presented. A distribution coefficient was also formulated which can be used to judge the suitability of a site for waste disposal. Moreover, a method for predicting contaminant concentration in groundwater at a site boundary is suggested for a heterogeneous media where the subsurface aquifer has different values of porosity, density, flow velocity, distribution coefficient and so on. A general equation was also developed to predict the distribution of radionuclides resulting from the disposal of a solid waste material. The distributions of contamination was evaluated for 90 Sr and 239 Pu which obey a linear adsorption model and a first order kinetics respectively. These equations appear to have practical utility for easily estimating groundwater contamination. (author)

Hydrogeochemical Modelling for Groundwater in Neyveli Aquifer, Tamil Nadu, India, Using PHREEQC: A Case Study

Energy Technology Data Exchange (ETDEWEB)

Chidambaram, S.; Anandhan, P. [Annamalai University, Department of Earth Sciences (India); Prasanna, M. V., E-mail: geoprasanna@gmail.com [Curtin University, Department of Applied Geology, School of Engineering and Science (Malaysia); Ramanathan, AL. [Jawaharlal Nehru University, School of Environmental Sciences (India); Srinivasamoorthy, K. [Pondicherry University, Department of Earth Sciences, School of Physical, Chemical and Applied Sciences (India); Senthil Kumar, G. [HNB Garwhal University, Department of Geology (India)

2012-09-15

Sophisticated geochemical models have been used to describe and predict the chemical behaviour of complex natural waters and also to protect the groundwater resources from future contamination. One such model is used to study the hydrogeochemical complexity in a mine area. Extraction of groundwater from the coastal aquifer has been in progress for decades to mine lignite in Neyveli. This extraction has developed a cone of depression around the mine site. This cone of depression is well established by the geochemical nature of groundwater in the region. 42 groundwater samples were collected in a definite pattern and they were analysed for major cations, anions and trace elements. The saturation index (SI) of the groundwater for carbonate, sulphate and silica minerals was studied and it has been correlated with the recharge and the discharge regions. The SI of alumino silicates has been used to decipher the stage of weathering. The SI{sub Gibbsite} - SI{sub K-feldspar} has been spatially distributed and the regions of discharge and recharge were identified. Then two flow paths A1 and A2 were identified and inverse modelling using PHREEQC were carried out to delineate the geochemical process that has taken place from recharge to discharge. The initial and final solutions in both the flow paths were correlated with the thermodynamic silicate stability diagrams of groundwater and it was found that the state of thermodynamic stability of the end solutions along the flow path were approaching similar states of equilibrium at the discharge.

Assessing the Vulnerability of Public-Supply Wells to Contamination: Floridan Aquifer System Near Tampa, Florida

Science.gov (United States)

Jagucki, Martha L.; Katz, Brian G.; Crandall, Christy A.; Eberts, Sandra M.

2009-01-01

This fact sheet highlights findings from the vulnerability study of a public-supply well in Temple Terrace, Florida, northeast of Tampa. The well selected for study typically produces water at the rate of 700 gallons per minute from the Upper Floridan aquifer. Water samples were collected at the public-supply well and at monitoring wells installed in or near the simulated zone of contribution to the supply well. Samples of untreated water from the public-supply wellhead contained the undesirable constituents nitrate, arsenic, uranium, radon-222, volatile organic compounds (VOCs), and pesticides, although all were detected at concentrations less than established drinking-water standards, where such standards exist. Overall, study findings point to four primary factors that affect the movement and fate of contaminants and the vulnerability of the public-supply well in Temple Terrace: (1) groundwater age (how long ago water entered, or recharged, the aquifer); (2) short-circuiting of contaminated water through sinkholes; (3) natural geochemical processes within the aquifer; and (4) pumping stress. Although the public-supply well is completed in the Upper Floridan aquifer, it produces water with concentrations of nitrate, VOCs, and the natural contaminant radon that are intermediate between the typical composition of water from the Upper Floridan aquifer and that of the overlying surficial aquifer system. Mixing calculations show that the water produced by the public-supply well could consist of upwards of 50 percent water from the surficial aquifer system mixed with water from the Upper Floridan aquifer. Anthropogenically affected water from the surficial aquifer system travels rapidly to depth through sinkholes that must be directly connected to the cavernous zone intersected by the public-supply well (and several other production wells in the region). Such solution features serve as fast pathways to the well and circumvent the natural attenuation of nitrate and

Results from a workshop on research needs for modeling aquifer thermal energy storage systems

Science.gov (United States)

Drost, M. K.

1990-08-01

A workshop an aquifer thermal energy storage (ATES) system modeling was conducted by Pacific Northwest Laboratory (PNL). The goal of the workshop was to develop a list of high priority research activities that would facilitate the commercial success of ATES. During the workshop, participants reviewed currently available modeling tools for ATES systems and produced a list of significant issues related to modeling ATES systems. Participants assigned a priority to each issue on the list by voting and developed a list of research needs for each of four high-priority research areas; the need for a feasibility study model, the need for engineering design models, the need for aquifer characterization, and the need for an economic model. The workshop participants concluded that ATES commercialization can be accelerated by aggressive development of ATES modeling tools and made specific recommendations for that development.

Aquifer thermal energy stores in Germany

International Nuclear Information System (INIS)

Kabus, F.; Seibt, P.; Poppei, J.

2000-01-01

This paper describes the state of essential demonstration projects of heat and cold storage in aquifers in Germany. Into the energy supply system of the buildings of the German Parliament in Berlin, there are integrated both a deep brine-bearing aquifer for the seasonal storage of waste heat from power and heat cogeneration and a shallow-freshwater bearing aquifer for cold storage. In Neubrandenburg, a geothermal heating plant which uses a 1.200 m deep aquifer is being retrofitted into an aquifer heat storage system which can be charged with the waste heat from a gas and steam cogeneration plant. The first centralised solar heating plant including an aquifer thermal energy store in Germany was constructed in Rostock. Solar collectors with a total area of 1000m 2 serve for the heating of a complex of buildings with 108 flats. A shallow freshwater-bearing aquifer is used for thermal energy storage. (Authors)

Organic and inorganic carbon dynamics in a karst aquifer: Santa Fe River Sink-Rise system, north Florida, USA

Science.gov (United States)

Jin, Jin; Zimmerman, Andrew R.; Moore, Paul J.; Martin, Jonathan B.

2014-03-01

Spatiotemporal variations in dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), major ions concentrations and other geochemical parameters including stable carbon isotopes of DIC (δ13CDIC), were measured in surface water and deep and shallow well water samples of the Santa Fe River Sink-Rise eogenetic karst system, north Florida, USA. Three end-member water sources were identified: one DOC-rich/DIC-poor/δ13CDIC-depleted, one DOC-poor/DIC-rich/δ13CDIC-enriched, and one enriched in major ions. Given their spatiotemporal distributions, they were presumed to represent soil water, upper aquifer groundwater, and deep aquifer water sources, respectively. Using assumed ratios of Na+, Cl, and SO42- for each end-member, a mixing model calculated the contribution of each water source to each sample. Then, chemical effects of biogeochemical reactions were calculated as the difference between those predicted by the mixing model and measured species concentrations. In general, carbonate mineral dissolution occurred throughout the Sink-Rise system, surface waters were net autotrophic and the subsurface was in metabolic balance, i.e., no net DOC or DIC production or consumption. However, there was evidence for chemolithoautotrophy, perhaps by hydrogen oxidizing microbes, at some deep aquifer sites. Mineralization of this autochthonous natural dissolved organic matter (NDOM) led to localized carbonate dissolution as did surface water-derived NDOM supplied to shallow well sites during the highest flow periods. This study demonstrates linkages between hydrology, abiotic and microbial processes and carbon dynamics and has important implications for groundwater quality, karst morphologic evolution, and hydrogeologic projects such as aquifer storage and recovery in karst systems.

Arsenic and radionuclide occurrence and relation to geochemistry in groundwater of the Gulf Coast Aquifer System in Houston, Texas, 2007–11

Science.gov (United States)

Oden, Jeannette H.; Szabo, Zoltan

2016-03-21

The U.S. Geological Survey (USGS), in cooperation with the City of Houston, began a study in 2007 to determine concentrations, spatial extent, and associated geochemical conditions that might be conducive for mobility and transport of selected naturally occurring trace elements and radionuclides in the Gulf Coast aquifer system in Houston, Texas. Water samples were collected from 91 municipal supply wells completed in the Evangeline and Chicot aquifers of the Gulf Coast aquifer system in northeastern, northwestern, and southwestern Houston; hereinafter referred to as northeast, northwest and southwest Houston areas. Wells were sampled in three phases: (1) 28 municipal supply wells were sampled during 2007–8, (2) 60 municipal supply wells during 2010, and (3) 3 municipal supply wells during December 2011. During each phase of sampling, samples were analyzed for major ions, selected trace elements, and radionuclides. At a subset of wells, concentrations of arsenic species and other radionuclides (carbon-14, radium-226, radium-228, radon-222, and tritium) also were analyzed. Selected physicochemical properties were measured in the field at the time each sample was collected, and oxidation-reduction potential and unfiltered sulfides also were measured at selected wells. The source-water (the raw, ambient water withdrawn from municipal supply wells prior to water treatment) samples were collected for assessment of aquifer conditions in order to provide community water-system operators information that could be important when they make decisions about which treatment processes to apply before distributing finished drinking water.

EPA Region 1 Sole Source Aquifers

Data.gov (United States)

U.S. Environmental Protection Agency — This coverage contains boundaries of EPA-approved sole source aquifers. Sole source aquifers are defined as an aquifer designated as the sole or principal source of...

Managed aquifer recharge in the Marecchia alluvial fan (Rimini - Italy, start of the test and first results

Directory of Open Access Journals (Sweden)

Paolo Severi

2014-09-01

Full Text Available Among the actions designed to manage the water crisis that have taken place in the summers of recent years in the southeastern part of the Emilia-Romagna Region, it has recently launched a trial of managed aquifer recharge in the alluvial fan of the Marecchia river (Rimini, where annually are withdrawn about 28 million m3 of water, 19 of witch for drinking water use. This test consists in conveying into quarry lake, located in the recharge area of the alluvial fan, an additional volume of water through a channel. The increase in the volume of water in the lake, should result in a rapid increase in the availability of water in the aquifers. To verify the recharge efficacy a special monitoring network consisting of 20 measuring points, 5 of which are specially drilled, it has been implemented. In 9 of these points a data logger for the continuous measure of level, temperature and electric conductivity at 20°C, it has been installed. A data logger has also been positioned in the channel from which the water flows into the lake. For about a month groundwater level was monitored prior to the recharge experiment. On 25 February 2014 managed aquifer recharge began and the volume of water flowing through the canal to lake until April 30, 2014, was approximately 600,000 m3. In this period it was possible to observe that the intervention produces the expected effects, thus inducing an increase in the groundwater level which is maximum near the lake and decreases away from it. The rise in the water level of the lake has been rapid and substantial. Within the area of the lake have settled some protected bird species in need of a precise environmental balance for nesting; an excessive increase of the lake level could put at risk of flooding some nests present. The objective of the following phases of the study will be to calibrate an adequate water level of the lake, to the purposes of managed aquifer recharge and to maintain the existing ecosystem. At the

Development and Modelling of a High-Resolution Aquifer Analog in the Guarani Aquifer (Brazil)

OpenAIRE

Höyng, Dominik

2014-01-01

A comprehensive and detailed knowledge about the spatial distribution of physical and chemical properties in heterogeneous porous aquifers plays a decisive role for a realistic representation of governing parameters in mathematical models. Models allow the simulation, prediction and reproduction of subsurface flow and transport characteristics. This work explains the identification, characterization and effects of small-scale aquifer heterogeneities in the Guarani Aquifer System (GAS) in S...

Sources of high-chloride water and managed aquifer recharge in an alluvial aquifer in California, USA

Science.gov (United States)

O'Leary, David R.; Izbicki, John A.; Metzger, Loren F.

2015-11-01

As a result of pumping in excess of recharge, water levels in alluvial aquifers within the Eastern San Joaquin Groundwater Subbasin, 130 km east of San Francisco (California, USA), declined below sea level in the early 1950s and have remained so to the present. Chloride concentrations in some wells increased during that time and exceeded the US Environmental Protection Agency's secondary maximum contaminant level of 250 mg/L, resulting in removal of some wells from service. Sources of high-chloride water include irrigation return in 16 % of sampled wells and water from delta sediments and deeper groundwater in 50 % of sampled wells. Chloride concentrations resulting from irrigation return commonly did not exceed 100 mg/L, although nitrate concentrations were as high as 25 mg/L as nitrogen. Chloride concentrations ranged from less than 100-2,050 mg/L in wells affected by water from delta sediments and deeper groundwater. Sequential electromagnetic logs show movement of high-chloride water from delta sediments to pumping wells through permeable interconnected aquifer layers. δD and δ18O data show most groundwater originated as recharge along the front of the Sierra Nevada, but tritium and carbon-14 data suggest recharge rates in this area are low and have decreased over recent geologic time. Managed aquifer recharge at two sites show differences in water-level responses to recharge and in the physical movement of recharged water with depth related to subsurface geology. Well-bore flow logs also show rapid movement of water from recharge sites through permeable interconnected aquifer layers to pumping wells.

Sources of high-chloride water and managed aquifer recharge in an alluvial aquifer in California, USA

Science.gov (United States)

O'Leary, David; Izbicki, John A.; Metzger, Loren F.

2015-01-01

As a result of pumping in excess of recharge, water levels in alluvial aquifers within the Eastern San Joaquin Groundwater Subbasin, 130 km east of San Francisco (California, USA), declined below sea level in the early 1950s and have remained so to the present. Chloride concentrations in some wells increased during that time and exceeded the US Environmental Protection Agency’s secondary maximum contaminant level of 250 mg/L, resulting in removal of some wells from service. Sources of high-chloride water include irrigation return in 16 % of sampled wells and water from delta sediments and deeper groundwater in 50 % of sampled wells. Chloride concentrations resulting from irrigation return commonly did not exceed 100 mg/L, although nitrate concentrations were as high as 25 mg/L as nitrogen. Chloride concentrations ranged from less than 100–2,050 mg/L in wells affected by water from delta sediments and deeper groundwater. Sequential electromagnetic logs show movement of high-chloride water from delta sediments to pumping wells through permeable interconnected aquifer layers. δD and δ18O data show most groundwater originated as recharge along the front of the Sierra Nevada, but tritium and carbon-14 data suggest recharge rates in this area are low and have decreased over recent geologic time. Managed aquifer recharge at two sites show differences in water-level responses to recharge and in the physical movement of recharged water with depth related to subsurface geology. Well-bore flow logs also show rapid movement of water from recharge sites through permeable interconnected aquifer layers to pumping wells.

Proceedings of the workshop on geochemical modeling

International Nuclear Information System (INIS)

1986-01-01

The following collection of papers was presented at a workshop on geochemical modeling that was sponsored by the Office of Civilian Radioactive Waste Management Program at the Lawrence Livermore National Laboratory (LLNL). The LLNL Waste Management Program sponsored this conference based on their belief that geochemical modeling is particularly important to the radioactive waste disposal project because of the need to predict the consequences of long-term water-rock interactions at the proposed repository site. The papers included in this volume represent a subset of the papers presented at the Fallen Leaf Lake Conference and cover a broad spectrum of detail and breadth in a subject that reflects the diverse research interests of the conference participants. These papers provide an insightful look into the current status of geochemical modeling and illustrate how various geochemical modeling codes have been applied to problems of geochemical interest. The emphasis of these papers includes traditional geochemical modeling studies of individual geochemical systems, the mathematical and theoretical development and refinement of new modeling capabilities, and enhancements of data bases on which the computations are based. The papers in this proceedings volume have been organized into the following four areas: Geochemical Model Development, Hydrothermal and Geothermal Systems, Sedimentary and Low Temperature Environments, and Data Base Development. The participants of this symposium and a complete list of the talks presented are listed in the appendices

Proceedings of the workshop on geochemical modeling

Energy Technology Data Exchange (ETDEWEB)

1986-01-01

The following collection of papers was presented at a workshop on geochemical modeling that was sponsored by the Office of Civilian Radioactive Waste Management Program at the Lawrence Livermore National Laboratory (LLNL). The LLNL Waste Management Program sponsored this conference based on their belief that geochemical modeling is particularly important to the radioactive waste disposal project because of the need to predict the consequences of long-term water-rock interactions at the proposed repository site. The papers included in this volume represent a subset of the papers presented at the Fallen Leaf Lake Conference and cover a broad spectrum of detail and breadth in a subject that reflects the diverse research interests of the conference participants. These papers provide an insightful look into the current status of geochemical modeling and illustrate how various geochemical modeling codes have been applied to problems of geochemical interest. The emphasis of these papers includes traditional geochemical modeling studies of individual geochemical systems, the mathematical and theoretical development and refinement of new modeling capabilities, and enhancements of data bases on which the computations are based. The papers in this proceedings volume have been organized into the following four areas: Geochemical Model Development, Hydrothermal and Geothermal Systems, Sedimentary and Low Temperature Environments, and Data Base Development. The participants of this symposium and a complete list of the talks presented are listed in the appendices.

Hydric results in Guarani Aquifer System formation zone through by hydrogeological monitoring in representative basin

International Nuclear Information System (INIS)

Wendland, E.; Barreto, C.; Gomes, L.; Dias Paiva, J.

2007-01-01

This work describes the direct and deep recharge in the Guarani Aquifer System, based on the evaluation of data acquired at the Ribeirao da Onca watershed, which is located at the outcrop zone of the GAS in Sao Paulo State, Brazil. During one year hydrological data (precipitation, temperature, discharge etc) have been monitored at the watershed. Using water level fluctuation measured in 23 monitoring wells, the direct recharge, the free aquifer storage and the base flow could be evaluated.The direct recharge of the system at the watershed has been estimated to 29% of the total precipitation in the period. Due to the drainage by the Ribeirao da Onca, the deep recharge, which effectively reaches the GAS, is reduced to 3,5% of the annual precipitation

Adsorption of phosphate from municipal effluents using cryptocrystalline magnesite: complementing laboratory results with geochemical modelling

CSIR Research Space (South Africa)

Masindi, Vhahangwele

2015-11-01

Full Text Available chemisorption. Adsorption isotherms fitted well to Langmuir adsorption isotherm than Freundlich adsorption isotherms, demonstrating monolayer adsorption. PHREEQC geochemical model showed Mg(sub3)(PO(sub4))(sub2) and MgHPO(sub4):3H(sub2)O as the phosphatebearing...

Summary of hydrologic testing of the Floridan aquifer system at Fort Stewart, coastal Georgia, 2009-2010

Science.gov (United States)

Gonthier, Gerald J.

2011-01-01

Two test wells were completed at Fort Stewart, coastal Georgia, to investigate the potential for using the Lower Floridan aquifer as a source of water to satisfy anticipated, increased water needs. The U.S. Geological Survey, in cooperation with the U.S. Department of the Army, completed hydrologic testing of the Floridan aquifer system at the study site, including flowmeter surveys, slug tests, and 24- and 72-hour aquifer tests by mid-March 2010. Analytical approaches and model simulation were applied to aquifer-test results to provide estimates of transmissivity and hydraulic conductivity of the multilayered Floridan aquifer system. Data from a 24-hour aquifer test of the Upper Floridan aquifer were evaluated by using the straight-line Cooper-Jacob analytical method. Data from a 72-hour aquifer test of the Lower Floridan aquifer were simulated by using axisymmetric model simulations. Results of aquifer testing indicated that the Upper Floridan aquifer has a transmissivity of 100,000 feet-squared per day, and the Lower Floridan aquifer has a transmissivity of 7,000 feet-squared per day. A specific storage for the Floridan aquifer system as a result of model calibration was 3E-06 ft–1. Additionally, during a 72-hour aquifer test of the Lower Floridan aquifer, a drawdown response was observed in two Upper Floridan aquifer wells, one of which was more than 1 mile away from the pumped well.

Sharp fronts within geochemical transport problems

International Nuclear Information System (INIS)

Grindrod, P.

1995-01-01

The authors consider some reactive geochemical transport problems in groundwater systems. When incoming fluid is in disequilibrium with the mineralogy sharp transition fronts may develop. They show that this is a generic property for a class of systems where the timescales associated with reaction and diffusion phenomena are much shorter than those associated with advective transport. Such multiple timescale problems are relevant to a variety of processes in natural systems: mathematically methods of singular perturbation theory reduce the dimension of the problems to be solved locally. Furthermore, they consider how spatial heterogeneous mineralogy can impact upon the propagation of sharp geochemical fronts. The authors developed an asymptotic approach in which they solve equations for the evolving geometry of the front and indicate how the non-smooth perturbations due to natural heterogeneity of the mineralogy on underlying ground water flow field are balanced against the smoothing effect of diffusion/dispersive processes. Fronts are curvature damped, and the results here indicate the generic nature of separate front propagation within both model (idealized) and natural (heterogeneous) geochemical systems

Direct-push geochemical profiling for assessment of inorganic chemical heterogeneity in aquifers

Science.gov (United States)

Schulmeister, M.K.; Healey, J.M.; Butler, J.J.; McCall, G.W.

2004-01-01

Discrete-depth sampling of inorganic groundwater chemistry is essential for a variety of site characterization activities. Although the mobility and rapid sampling capabilities of direct-push techniques have led to their widespread use for evaluating the distribution of organic contaminants, complementary methods for the characterization of spatial variations in geochemical conditions have not been developed. In this study, a direct-push-based approach for high-resolution inorganic chemical profiling was developed at a site where sharp chemical contrasts and iron-reducing conditions had previously been observed. Existing multilevel samplers (MLSs) that span a fining-upward alluvial sequence were used for comparison with the direct-push profiling. Chemical profiles obtained with a conventional direct-push exposed-screen sampler differed from those obtained with an adjacent MLS because of sampler reactivity and mixing with water from previous sampling levels. The sampler was modified by replacing steel sampling components with stainless-steel and heat-treated parts, and adding an adapter that prevents mixing. Profiles obtained with the modified approach were in excellent agreement with those obtained from an adjacent MLS for all constituents and parameters monitored (Cl, NO3, Fe, Mn, DO, ORP, specific conductance and pH). Interpretations of site redox conditions based on field-measured parameters were supported by laboratory analysis of dissolved Fe. The discrete-depth capability of this approach allows inorganic chemical variations to be described at a level of detail that has rarely been possible. When combined with the mobility afforded by direct-push rigs and on-site methods of chemical analysis, the new approach is well suited for a variety of interactive site-characterization endeavors. ?? 2003 Elsevier B.V. All rights reserved.

Investigating river–aquifer relations using water temperature in an anthropized environment (Motril-Salobreña aquifer)

DEFF Research Database (Denmark)

Duque, Carlos; Calvache, Marie; Engesgaard, Peter Knudegaard

2010-01-01

Heat was applied as a tracer for determining river–aquifer relations in the Motril-Salobreña aquifer (S Spain). The aquifer has typically been recharged by River Guadalfeo infiltration, nevertheless from 2005 a dam was constructed changing the traditional dynamic river flow and recharge events...

Groundwaters of Florence (Italy): Trace element distribution and vulnerability of the aquifers

Science.gov (United States)

Bencini, A.; Ercolanelli, R.; Sbaragli, A.; Verrucchi, C.

1993-11-01

Geochemical and hydrogeological research has been carried out on 109 wells in the alluvial plain of Florence, in order to evaluate conductivity and main chemistry of ground waters, the pattern of some possible pollutant chemical species (Fe, Mn, Cr, Cu, Pb, Zn, NO2, NO3), and the vulnerability of the aquifers. The plain is made up of Plio-Quaternary alluvial and lacustrine sediments for a maximum thickness of 600 m. Silts and clays, sometimes with lenses of sandy gravels, are dominant, while considerable deposits of sands, pebbles, and gravels occur along the course of the Arno river and its tributary streams, and represent the most important aquifer of the plain. The groundwaters analyzed belong to this aquifer or to the smaller ones, hosted in the gravel lenses. Most waters show conductivity values around 1000 1200 μS, and almost all of them have an alkaline-earth-bicarbonate chemical character; these features are consistent with the mainly calcareous lithology of the aquifers. In the western areas a higher salt content of the groundwaters is evident, probably related to the presence of industrial activities which use water desalinators. Heavy metal and NO2, NO3 analyses point out that no important pollution phenomena affect the groundwaters; all the mean values of the chemical considered species are below the maximum admissible concentration (MAC) fixed by the European Community for drinkable waters. Nevertheless, some anomalies of NO2, NO3, Fe, Mn, and Zn are present in the plain. Apart from Mn, which seems to be released by certain calcareous gravels, the other anomalies have a local influence, since they disappear even in the nearest wells. The most plausible causes can be recognized in losses of the sewage system (NO2=3 4 mg/t); use of nitrate compounds in agriculture (NO3=60 70 mg/l); oxidation of well pipes (Fe ≈ 20 mg/l; Zn ≈ 6 mg/l). As regards Cr, Cu, and Pb, all the observations are below the MAC; therefore, the median values of bacteria oxidation

Review of Aquifer Storage and Recovery Performance in the Upper Floridan Aquifer in Southern Florida

Science.gov (United States)

Reese, Ronald S.

2006-01-01

Introduction: Interest and activity in aquifer storage and recovery (ASR) in southern Florida has increased greatly during the past 10 to 15 years. ASR wells have been drilled to the carbonate Floridan aquifer system at 30 sites in southern Florida, mostly by local municipalities or counties located in coastal areas. The primary storage zone at these sites is contained within the brackish to saline Upper Floridan aquifer of the Floridan aquifer system. The strategy for use of ASR in southern Florida is to store excess freshwater available during the wet season in an aquifer and recover it during the dry season when needed for supplemental water supply. Each ASR cycle is defined by three periods: recharge, storage, and recovery. This fact sheet summarizes some of the findings of a second phase retrospective assessment of existing ASR facilities and sites.

Geologic CO2 Sequestration: Predicting and Confirming Performance in Oil Reservoirs and Saline Aquifers

Science.gov (United States)

Johnson, J. W.; Nitao, J. J.; Newmark, R. L.; Kirkendall, B. A.; Nimz, G. J.; Knauss, K. G.; Ziagos, J. P.

2002-05-01

Reducing anthropogenic CO2 emissions ranks high among the grand scientific challenges of this century. In the near-term, significant reductions can only be achieved through innovative sequestration strategies that prevent atmospheric release of large-scale CO2 waste streams. Among such strategies, injection into confined geologic formations represents arguably the most promising alternative; and among potential geologic storage sites, oil reservoirs and saline aquifers represent the most attractive targets. Oil reservoirs offer a unique "win-win" approach because CO2 flooding is an effective technique of enhanced oil recovery (EOR), while saline aquifers offer immense storage capacity and widespread distribution. Although CO2-flood EOR has been widely used in the Permian Basin and elsewhere since the 1980s, the oil industry has just recently become concerned with the significant fraction of injected CO2 that eludes recycling and is therefore sequestered. This "lost" CO2 now has potential economic value in the growing emissions credit market; hence, the industry's emerging interest in recasting CO2 floods as co-optimized EOR/sequestration projects. The world's first saline aquifer storage project was also catalyzed in part by economics: Norway's newly imposed atmospheric emissions tax, which spurred development of Statoil's unique North Sea Sleipner facility in 1996. Successful implementation of geologic sequestration projects hinges on development of advanced predictive models and a diverse set of remote sensing, in situ sampling, and experimental techniques. The models are needed to design and forecast long-term sequestration performance; the monitoring techniques are required to confirm and refine model predictions and to ensure compliance with environmental regulations. We have developed a unique reactive transport modeling capability for predicting sequestration performance in saline aquifers, and used it to simulate CO2 injection at Sleipner; we are now

Porosity Development in a Coastal Setting: A Reactive Transport Model to Assess the Influence of Heterogeneity of Hydrological, Geochemical and Lithological Conditions

Science.gov (United States)

Maqueda, A.; Renard, P.; Cornaton, F. J.

2014-12-01

Coastal karst networks are formed by mineral dissolution, mainly calcite, in the freshwater-saltwater mixing zone. The problem has been approached first by studying the kinetics of calcite dissolution and then coupling ion-pairing software with flow and mass transport models. Porosity development models require high computational power. A workaround to reduce computational complexity is to assume the calcite dissolution reaction is relatively fast, thus equilibrium chemistry can be used to model it (Sanford & Konikow, 1989). Later developments allowed the full coupling of kinetics and transport in a model. However kinetics effects of calcite dissolution were found negligible under the single set of assumed hydrological and geochemical boundary conditions. A model is implemented with the coupling of FeFlow software as the flow & transport module and PHREEQC4FEFLOW (Wissmeier, 2013) ion-pairing module. The model is used to assess the influence of heterogeneities in hydrological, geochemical and lithological boundary conditions on porosity evolution. The hydrologic conditions present in the karst aquifer of Quintana Roo coast in Mexico are used as a guide for generating inputs for simulations.

Hydrogeological modeling constraints provided by geophysical and geochemical mapping of a chlorinated ethenes plume in northern France

Science.gov (United States)

Razafindratsima, Stephen; Guérin, Roger; Bendjoudi, Hocine; de Marsily, Ghislain

2014-09-01

A methodological approach is described which combines geophysical and geochemical data to delineate the extent of a chlorinated ethenes plume in northern France; the methodology was used to calibrate a hydrogeological model of the contaminants' migration and degradation. The existence of strong reducing conditions in some parts of the aquifer is first determined by measuring in situ the redox potential and dissolved oxygen, dissolved ferrous iron and chloride concentrations. Electrical resistivity imaging and electromagnetic mapping, using the Slingram method, are then used to determine the shape of the pollutant plume. A decreasing empirical exponential relation between measured chloride concentrations in the water and aquifer electrical resistivity is observed; the resistivity formation factor calculated at a few points also shows a major contribution of chloride concentration in the resistivity of the saturated porous medium. MODFLOW software and MT3D99 first-order parent-daughter chain reaction and the RT3D aerobic-anaerobic model for tetrachloroethene (PCE)/trichloroethene (TCE) dechlorination are finally used for a first attempt at modeling the degradation of the chlorinated ethenes. After calibration, the distribution of the chlorinated ethenes and their degradation products simulated with the model approximately reflects the mean measured values in the observation wells, confirming the data-derived image of the plume.

Groundwater Contamination by Uranium and Mercury at the Ridaura Aquifer (Girona, NE Spain

Directory of Open Access Journals (Sweden)

Andrés Navarro

2016-08-01

Full Text Available Elevated concentrations of uranium and mercury have been detected in drinking water from public supply and agricultural wells in alluvial and granitic aquifers of the Ridaura basin located at Catalan Coastal Ranges (CCR. The samples showed high concentrations of U above the U.S. standards and the World Health Organization regulations which set a maximum value of 30 µg/L. Further, high mercury concentrations above the European Drinking Water Standards (1 μg/L were found. Spatial distribution of U in groundwater and geochemical evolution of groundwater suggest that U levels appear to be highest in granitic areas where groundwater has long residence times and a significant salinity. The presence of high U concentrations in alluvial groundwater samples could be associated with hydraulic connection through fractures between the alluvial system and deep granite system. According to this model, oxidizing groundwater moving through fractures in the leucocratic/biotitic granite containing anomalous U contents are the most likely to acquire high levels of U. The distribution of Hg showed concentrations above 1 μg/L in 10 alluvial samples, mainly located near the limit of alluvial aquifer with igneous rocks, which suggests a possible migration of Hg from granitic materials. Also, some samples showed Hg concentrations comprised between 0.9 and 1.5 μg/L, from wells located in agricultural areas.

Geochemical baseline studies of soil in Finland

Science.gov (United States)

Pihlaja, Jouni

2017-04-01

The soil element concentrations regionally vary a lot in Finland. Mostly this is caused by the different bedrock types, which are reflected in the soil qualities. Geological Survey of Finland (GTK) is carrying out geochemical baseline studies in Finland. In the previous phase, the research is focusing on urban areas and mine environments. The information can, for example, be used to determine the need for soil remediation, to assess environmental impacts or to measure the natural state of soil in industrial areas or mine districts. The field work is done by taking soil samples, typically at depth between 0-10 cm. Sampling sites are chosen to represent the most vulnerable areas when thinking of human impacts by possible toxic soil element contents: playgrounds, day-care centers, schools, parks and residential areas. In the mine districts the samples are taken from the areas locating outside the airborne dust effected areas. Element contents of the soil samples are then analyzed with ICP-AES and ICP-MS, Hg with CV-AAS. The results of the geochemical baseline studies are published in the Finnish national geochemical baseline database (TAPIR). The geochemical baseline map service is free for all users via internet browser. Through this map service it is possible to calculate regional soil baseline values using geochemical data stored in the map service database. Baseline data for 17 elements in total is provided in the map service and it can be viewed on the GTK's web pages (http://gtkdata.gtk.fi/Tapir/indexEN.html).

Alligator Rivers Analogue project. Geochemical Data Bases

International Nuclear Information System (INIS)

Bennett, D.G.; Read, D.

1992-01-01

The Koongarra uranium deposit in the Northern Territory of Australia is being studied to evaluate the processes involved in the geochemical alteration of the ore body and the formation of the uranium dispersion fan. A broad range of research is being undertaken into the geochemistry and hydrology of the site with the aim of understanding the transport of radionuclides through the system. During the project a range of geochemical and hydrogeochemical models have been developed to account for measured data from the site and with which to predict site evolution. The majority of these models are based on the premise of thermodynamic chemical equilibrium and employ fundamental thermodynamic data to characterise the chemistry of the system. From the differences which exist between the thermodynamic data bases (Appendices I and II) it is possible to gain a view of the level of uncertainty associated with thermodynamic data in each set of calculations. This report gives a brief introduction to the geochemical processes underlying the models, and details the equations used to quantify the more common of these processes (e.g. aqueous speciation and mineral solubility). A description is given of the computer codes (EQ3/6, PHREEQE, MINTEQ) most commonly used during the project for geochemical modelling. Their key features are highlighted and comparisons made. It is concluded that the degree of uncertainty in geochemical modelling studies arising as a result of using one code rather than another is relatively insignificant when compared to that related to differences in the underlying data bases. 73 refs., 3 figs

Simulated effects of groundwater withdrawals from the Kirkwood-Cohansey aquifer system and Piney Point aquifer, Maurice and Cohansey River Basins, Cumberland County and vicinity, New Jersey

Science.gov (United States)

Gordon, Alison D.; Buxton, Debra E.

2018-05-10

groundwater demand in 2050 at municipal public-supply wells; and (5) estimated 2050 monthly groundwater demand at municipal public-supply wells for which pumping of selected municipal public-supply wells was moved to a deeper part of the Kirkwood-Cohansey aquifer system. The results of the baseline scenario (scenario 1) were used for comparison with the results of scenarios 2‒5.The results of scenarios 2‒3 indicate that simulated water-level declines occurred in the Cohansey River Basin when full-allocation groundwater withdrawals were incorporated (scenarios 2 and 3). In scenarios 2 and 3, full-allocation withdrawals in the Cohansey River Basin were approximately 266 and 407 percent greater, respectively, than in the baseline scenario. In scenario 2, the largest decline in simulated water levels was more than 67 ft in June and September of scenario year 11, whereas in scenario 3, simulated water levels declined as much as 90 ft in June and more than 100 ft in September of scenario year 11. These simulated declines occurred in a small area around one pumped well in the Cohansey River Basin. The average decline in simulated water levels for this basin was less than 10 ft for scenario 2 and less than 20 ft for scenario 3. In scenario 2, the Menantico Creek subbasin in the Maurice River Basin had a decrease in base flow during about 29 percent of the 11-year simulation period, and in scenario 3, the decrease occurred during about 71 percent of the 11-year simulation period. In scenario 3, base flow in the Cohansey River Basin was less than the 7-day 10-year low flow in all months of simulation years 7 through 11. Several agricultural-irrigation wells and a number of public-supply wells are within the Cohansey River Basin and the Menantico Creek subbasin.Three additional scenarios were simulated to evaluate the possible use of the Piney Point aquifer in the Cumberland County study area using the New Jersey Regional Aquifer-System Analysis model, which incorporates all

Impact of climate changes during the last 5 million years on groundwater in basement aquifers.

Science.gov (United States)

Aquilina, Luc; Vergnaud-Ayraud, Virginie; Les Landes, Antoine Armandine; Pauwels, Hélène; Davy, Philippe; Pételet-Giraud, Emmanuelle; Labasque, Thierry; Roques, Clément; Chatton, Eliot; Bour, Olivier; Ben Maamar, Sarah; Dufresne, Alexis; Khaska, Mahmoud; Le Gal La Salle, Corinne; Barbecot, Florent

2015-09-22

Climate change is thought to have major effects on groundwater resources. There is however a limited knowledge of the impacts of past climate changes such as warm or glacial periods on groundwater although marine or glacial fluids may have circulated in basements during these periods. Geochemical investigations of groundwater at shallow depth (80-400 m) in the Armorican basement (western France) revealed three major phases of evolution: (1) Mio-Pliocene transgressions led to marine water introduction in the whole rock porosity through density and then diffusion processes, (2) intensive and rapid recharge after the glacial maximum down to several hundred meters depths, (3) a present-day regime of groundwater circulation limited to shallow depth. This work identifies important constraints regarding the mechanisms responsible for both marine and glacial fluid migrations and their preservation within a basement. It defines the first clear time scales of these processes and thus provides a unique case for understanding the effects of climate changes on hydrogeology in basements. It reveals that glacial water is supplied in significant amounts to deep aquifers even in permafrosted zones. It also emphasizes the vulnerability of modern groundwater hydrosystems to climate change as groundwater active aquifers is restricted to shallow depths.

Groundwater chemistry and occurrence of arsenic in the Meghna floodplain aquifer, southeastern Bangladesh

Science.gov (United States)

Zahid, A.; Hassan, M.Q.; Balke, K.-D.; Flegr, M.; Clark, D.W.

2008-01-01

Dissolved major ions and important heavy metals including total arsenic and iron were measured in groundwater from shallow (25-33 m) and deep (191-318 m) tube-wells in southeastern Bangladesh. These analyses are intended to help describe geochemical processes active in the aquifers and the source and release mechanism of arsenic in sediments for the Meghna Floodplain aquifer. The elevated Cl- and higher proportions of Na+ relative to Ca2+, Mg2+, and K+ in groundwater suggest the influence by a source of Na+ and Cl-. Use of chemical fertilizers may cause higher concentrations of NH 4+ and PO 43- in shallow well samples. In general, most ions are positively correlated with Cl-, with Na+ showing an especially strong correlation with Cl-, indicating that these ions are derived from the same source of saline waters. The relationship between Cl-/HCO 3- ratios and Cl- also shows mixing of fresh groundwater and seawater. Concentrations of dissolved HCO 3- reflect the degree of water-rock interaction in groundwater systems and integrated microbial degradation of organic matter. Mn and Fe-oxyhydroxides are prominent in the clayey subsurface sediment and well known to be strong adsorbents of heavy metals including arsenic. All five shallow well samples had high arsenic concentration that exceeded WHO recommended limit for drinking water. Very low concentrations of SO 42- and NO 3- and high concentrations of dissolved Fe and PO 43- and NH 4+ ions support the reducing condition of subsurface aquifer. Arsenic concentrations demonstrate negative co-relation with the concentrations of SO 42- and NO 3- but correlate weakly with Mo, Fe concentrations and positively with those of P, PO 43- and NH 4+ ions. ?? 2007 Springer-Verlag.

Geospatial compilation of historical water-level changes in the Chicot and Evangeline aquifers 1977-2013 and Jasper aquifer 2000-13, Gulf Coast aquifer system, Houston-Galveston region, Texas

Science.gov (United States)

Johnson, Michaela R.; Linard, Joshua I.

2014-01-01

The U.S. Geological Survey (USGS) in cooperation with the Harris-Galveston Subsidence District, City of Houston, Fort Bend Subsidence District, Lone Star Groundwater Conservation District, and Brazoria County Groundwater Conservation District has produced an annual series of reports that depict water-level changes in the Chicot, Evangeline, and Jasper aquifers of the Gulf Coast aquifer system in the Houston-Galveston region, Texas, from 1977 to 2013. Changes are determined from water-level measurements between December and March of each year from groundwater wells screened in one of the three aquifers. Existing published maps and unpublished geographic information system (GIS) datasets were compiled into a comprehensive geodatabase of all water-level-change maps produced as part of this multiagency effort. Annual water-level-change maps were georeferenced and digitized where existing GIS data were unavailable (1979–99). Existing GIS data available for 2000–13 were included in the geodatabase. The compilation contains 121 datasets showing water-level changes for each primary aquifer of the Gulf Coast aquifer system: 56 for the Chicot aquifer (1977; 1979–2013 and 1990; 1993–2013), 56 for the Evangeline aquifer (1977; 1979–2013 and 1990; 1993–2013), and 9 for the Jasper aquifer (2000; 2005–13).

Guarani aquifer

International Nuclear Information System (INIS)

2007-01-01

The environmental protection and sustain ability develop project of Guarani Aquifer System is a join work from Argentina, Brazil, Paraguay and Uruguay with a purpose to increase the knowledge resource and propose technical legal and organizational framework for sustainable management between countries.The Universities funds were created as regional universities support in promotion, training and academic research activities related to environmental al social aspects of the Guarani Aquifer System.The aim of the project is the management and protection of the underground waters resources taking advantage and assesment for nowadays and future generations

ALOPEX stochastic optimization for pumping management in fresh water coastal aquifers

International Nuclear Information System (INIS)

Stratis, P N; Saridakis, Y G; Zakynthinaki, M S; Papadopoulou, E P

2014-01-01

Saltwater intrusion in freshwater aquifers is a problem of increasing significance in areas nearby the coastline. Apart from natural disastrous phenomena, such as earthquakes or floods, intense pumping human activities over the aquifer areas may change the chemical composition of the freshwater aquifer. Working towards the direction of real time management of freshwater pumping from coastal aquifers, we have considered the deployment of the stochastic optimization Algorithm of Pattern Extraction (ALOPEX), coupled with several penalty strategies that produce convenient management policies. The present study, which further extents recently derived results, considers the analytical solution of a classical model for underground flow and the ALOPEX stochastic optimization technique to produce an efficient approach for pumping management over coastal aquifers. Numerical experimentation also includes a case study at Vathi area on the Greek island of Kalymnos, to compare with known results in the literature as well as to demonstrate different management strategies