Decadal-scale changes in dissolved-solids concentrations in groundwater used for public supply, Salt Lake Valley, Utah

Science.gov (United States)

Thiros, Susan A.; Spangler, Larry

2010-01-01

Basin-fill aquifers are a major source of good-quality water for public supply in many areas of the southwestern United States and have undergone increasing development as populations have grown over time. During 2005, the basin-fill aquifer in Salt Lake Valley, Utah, provided approximately 75,000 acre-feet, or about 29 percent of the total amount of water used by a population of 967,000. Groundwater in the unconsolidated basin-fill deposits that make up the aquifer occurs under unconfined and confined conditions. Water in the shallow unconfined part of the groundwater system is susceptible to near-surface contamination and generally is not used as a source of drinking water. Groundwater for public supply is withdrawn from the deeper unconfined and confined parts of the system, termed the principal aquifer, because yields generally are greater and water quality is better (including lower dissolved-solids concentrations) than in the shallower parts of the system. Much of the water in the principal aquifer is derived from recharge in the adjacent Wasatch Range (mountain-block recharge). In many areas, the principal aquifer is separated from the overlying shallow aquifer by confining layers of less permeable, fine-grained sediment that inhibit the downward movement of water and any potential contaminants from the surface. Nonetheless, under certain hydrologic conditions, human-related activities can increase dissolved-solids concentrations in the principal aquifer and result in groundwater becoming unsuitable for consumption without treatment or mixing with water having lower dissolved-solids concentrations. Dissolved-solids concentrations in areas of the principal aquifer used for public supply typically are less than 500 milligrams per liter (mg/L), the U.S. Environmental Protection Agency (EPA) secondary (nonenforceable) drinking-water standard. However, substantial increases in dissolved-solids concentrations in the principal aquifer have been documented in some

Dissolved Organic Carbon 14C in Southern Nevada Groundwater and Implications for Groundwater Travel Times

Energy Technology Data Exchange (ETDEWEB)

Hershey, Ronald L. [Nevada University, Reno, NV (United States). Desert Research Institute; Fereday, Wyall [Nevada University, Reno, NV (United States). Desert Research Institute; Thomas, James M [Nevada University, Reno, NV (United States). Desert Research Institute

2016-08-01

Dissolved inorganic carbon (DIC) carbon-14 (¹⁴C) ages must be corrected for complex chemical and physical reactions and processes that change the amount of ¹⁴C in groundwater as it flows from recharge to downgradient areas. Because of these reactions, DIC ¹⁴C can produce unrealistically old ages and long groundwater travel times that may, or may not, agree with travel times estimated by other methods. Dissolved organic carbon (DOC) ¹⁴C ages are often younger than DIC ¹⁴C ages because there are few chemical reactions or physical processes that change the amount of DOC ¹⁴C in groundwater. However, there are several issues that create uncertainty in DOC ¹⁴C groundwater ages including limited knowledge of the initial (A₀) DOC ¹⁴C in groundwater recharge and potential changes in DOC composition as water moves through an aquifer. This study examines these issues by quantifying A₀ DOC ¹⁴C in recharge areas of southern Nevada groundwater flow systems and by evaluating changes in DOC composition as water flows from recharge areas to downgradient areas. The effect of these processes on DOC ¹⁴C groundwater ages is evaluated and DOC and DIC ¹⁴C ages are then compared along several southern Nevada groundwater flow paths. Twenty-seven groundwater samples were collected from springs and wells in southern Nevada in upgradient, midgradient, and downgradient locations. DOC ¹⁴C for upgradient samples ranged from 96 to 120 percent modern carbon (pmc) with an average of 106 pmc, verifying modern DOC ¹⁴C ages in recharge areas, which decreases uncertainty in DOC ¹⁴C A₀ values, groundwater ages, and travel times. The HPLC spectra of groundwater along a flow path in the Spring Mountains show the same general pattern indicating that the DOC compound composition does not change along this flow path

Field Tests of Real-time In-situ Dissolved CO2 Monitoring for CO2 Leakage Detection in Groundwater

Science.gov (United States)

Yang, C.; Zou, Y.; Delgado, J.; Guzman, N.; Pinedo, J.

2016-12-01

Groundwater monitoring for detecting CO2 leakage relies on groundwater sampling from water wells drilled into aquifers. Usually groundwater samples are required be collected periodically in field and analyzed in the laboratory. Obviously groundwater sampling is labor and cost-intensive for long-term monitoring of large areas. Potential damage and contamination of water samples during the sampling process can degrade accuracy, and intermittent monitoring may miss changes in the geochemical parameters of groundwater, and therefore signs of CO2 leakage. Real-time in-situ monitoring of geochemical parameters with chemical sensors may play an important role for CO2 leakage detection in groundwater at a geological carbon sequestration site. This study presents field demonstration of a real-time in situ monitoring system capable of covering large areas for detection of low levels of dissolved CO2 in groundwater and reliably differentiating natural variations of dissolved CO2 concentration from small changes resulting from leakage. The sand-alone system includes fully distributed fiber optic sensors for carbon dioxide detection with a unique sensor technology developed by Intelligent Optical Systems. The systems were deployed to the two research sites: the Brackenridge Field Laboratory where the aquifer is shallow at depths of 10-20 ft below surface and the Devine site where the aquifer is much deeper at depths of 140 to 150 ft. Groundwater samples were periodically collected from the water wells which were installed with the chemical sensors and further compared to the measurements of the chemical sensors. Our study shows that geochemical monitoring of dissolved CO2 with fiber optic sensors could provide reliable CO2 leakage signal detection in groundwater as long as CO2 leakage signals are stronger than background noises at the monitoring locations.

Dissolved gasesous hydrocarbons in shallow groundwater of Lower Saxony, Germany - Revisited 2016

Science.gov (United States)

Schloemer, Stefan; Illing, Christian J.; Blumenberg, Martin; Oest, Johanna; Elbracht, Jörg

2017-04-01

Many concerns arise within the public and government/political institutions over potential groundwater contamination from deep drilling operations. For this reason we initiated a baseline study in 2014 on the distribution of dissolved methane, ethane and propane in shallow groundwater ( 1000 groundwater wells, Schloemer et al., 2016) of Lower Saxony, which includes the major petroleum and natural gas provinces in Germany. We observed a variation of dissolved methane concentration over 7 orders of magnitude (20 nl/l to 60 ml/l [v/v]). Methane delta13C compositions ranged from -110‰ to +25‰ vs VPDB, narrowly clustering around -70‰ at high concentrations but being increasingly more variable at lower concentrations (-40‰ to -80‰)). Most of the data are clearly indicative for methanogenic processes, samples unusually enriched in delta13C can best be explained by secondary methane oxidation. Although some general regional trend can be observed, results are highly variable within short lateral distances or within different aquifers/filter depths. Frequently ethane (27% of samples, median 50nl/l) and occasionally propane (8%, median 23nl/l) has been detected. Lacking the carbon isotope composition of these homologues and thus solely based on the extremely low concentrations and atypical ethane/propane ratios, these have been tentatively interpreted as ubiquitous microbial background. From the original 2014 sample set around 100 wells have been selected for consecutive testing through 2015. In spring 2016 a total number of 1100 wells have been sampled, 700 of which had already been part of the initial study, providing us with the unique opportunity to assess long term variations. The overall comparison of these 700 samples revealed only small relative variations in methane concentrations (mostly ± 5‰ in 25% of samples). Minor variations could be related to uncertainties in laboratory analysis (± 10% in concentration, ± 0.5‰ delta13C). To which extent the

Source and Processes of Dissolved Organic Matter in a Bangladesh Groundwater

Science.gov (United States)

McKnight, D. M.; Simone, B. E.; Mladenov, N.; Zheng, Y.; Legg, T. M.; Nemergut, D.

2010-12-01

Arsenic contamination of groundwater is a global health crisis, especially in Bangladesh where an estimated 40 million people are at risk. The release of geogenic arsenic bound to sediments into groundwater is thought to be influenced by dissolved organic matter (DOM) through several biogeochemical processes. Abiotically, DOM can promote the release of sediment bound As through the formation of DOM-As complexes and competitive interactions between As and DOM for sorption sites on the sediment. Additionally, the labile portion of groundwater DOM can serve as an electron donor to support microbial growth and the more recalcitrant humic DOM may serve as an electron shuttle, facilitating the eventual reduction of ferric iron present as iron oxides in sediments and consequently the mobilization of sorbed As and organic material. The goal of this study is to understand the source of DOM in representative Bangladesh groundwaters and the DOM sorption processes that occur at depth. We report chemical characteristics of representative DOM from a surface water, a shallow low-As groundwater, mid-depth high-As groundwater from the Araihazar region of Bangladesh. The humic DOM from groundwater displayed a more terrestrial chemical signature, indicative of being derived from plant and soil precursor materials, while the surface water humic DOM had a more microbial signature, suggesting an anthropogenic influence. In terms of biogeochemical processes occurring in the groundwater system, there is evidence from a diverse set of chemical characteristics, ranging from 13C-NMR spectroscopy to the analysis of lignin phenols, for preferential sorption onto iron oxides influencing the chemistry and reactivity of humic DOM in high As groundwater in Bangladesh. Taken together, these results provide chemical evidence for anthropogenic influence and the importance of sorption reactions at depth controlling the water quality of high As groundwater in Bangladesh.

Initial site characterisation of a dissolved hydrocarbon groundwater plume discharging to a surface water environment

International Nuclear Information System (INIS)

Westbrook, S.J.; Commonwealth Scientific and Industrial Research Organisation Land and Water, Wembley, WA; Davis, G.B.; Rayner, J.L.; Fisher, S.J.; Clement, T.P.

2000-01-01

Preliminary characterisation of a dissolved hydrocarbon groundwater plume flowing towards a tidally- and seasonally-forced estuarine system has been completed at a site in Perth, Western Australia. Installation and sampling of multiport boreholes enabled fine scale (0.5-m) vertical definition of hydrocarbon concentrations. Vertical electrical conductivity profiles from multiport and spear probe sampling into the river sediments indicated that two groundwater/river water interfaces or dispersion zones are present: (a) an upper dispersion zone between brackish river water and groundwater, and (b) a lower interface between groundwater and deeper saline water. On-line water level loggers show that near-shore groundwater levels are also strongly influence by tidal oscillation. Results from the initial site characterisation will be used to plan further investigations of contaminated groundwater/surface water interactions and the biodegradation processes occurring at the site

Determination of dissolved gases in basalt groundwater in the Pasco Basin, Washington

International Nuclear Information System (INIS)

Halko, D.J.

1986-09-01

The determination of dissolved gases in groundwater is required for complete hydrochemical characterization of the Columbia River Basalt Group beneath the Hanford Site. A gas chromatographic method has been developed for the determination of argon, oxygen, nitrogen, carbon monoxide, carbon dioxide, and methane in groundwater. In addition to a gas chromatograph equipped with thermal conductivity and flame ionization detectors, equipment utilized consists of a purge device that strips these gases from solution for subsequent separation using Molecular Sieve 5A and porous polymer columns. This technique is capable of accommodating pressurized fluid samples collected from the deep aquifers with in situ samplers. The analysis is discussed in detail

The effect of microbial activity and adsorption processes on groundwater dissolved organic carbon character and concentration

Science.gov (United States)

Meredith, K.; McDonough, L.; Oudone, P.; Rutlidge, H.; O'Carroll, D. M.; Andersen, M. S.; Baker, A.

2017-12-01

Balancing the terrestrial global carbon budget has proven to be a significant challenge. Whilst the movement of carbon in the atmosphere, rivers and oceans has been extensively studied, the potential for groundwater to act as a carbon source or sink through both microbial activity and sorption to and from mineral surfaces, is poorly understood. To investigate the biodegradable component of groundwater dissolved organic carbon (DOC), groundwater samples were collected from multiple coastal and inland sites. Water quality parameters such as pH, electrical conductivity, temperature, dissolved oxygen were measured in the field. Samples were analysed and characterised for their biodegradable DOC content using spectrofluorometric and Liquid Chromatography-Organic Carbon Detection (LC-OCD) techniques at set intervals within a 28 day period. Further to this, we performed laboratory sorption experiments on our groundwater samples using different minerals to examine the effect of adsorption processes on DOC character and concentration. Calcium carbonate, quartz and iron coated quartz were heated to 400ºC to remove potential carbon contamination, and then added at various known masses (0 mg to 10 g) to 50 mL of groundwater. Samples were then rotated for two hours, filtered at 0.2 μm and analysed by LC-OCD. This research forms part of an ongoing project which will assist in identifying the factors affecting the mobilisation, transport and removal of DOC in uncontaminated groundwater. By quantifying the relative importance of these processes, we can then determine whether the groundwater is a carbon source or sink. Importantly, this information will help guide policy and identify the need to include groundwater resources as part of the carbon economy.

Passive sampling and analyses of common dissolved fixed gases in groundwater

International Nuclear Information System (INIS)

Spalding, Brian Patrick; Watson, David B.

2008-01-01

An in situ passive sampler and gas chromatographic protocol for analysis of the major and several minor fixed gases in groundwater was developed. A gas-tight syringe, mated to a short length of silicone tubing, was equilibrated with dissolved gases in groundwater by immersing in monitoring wells and was used to transport and to inject a 0.5 mL gas sample into a gas chromatograph. Using Ar carrier gas, a HaySep DB porous polymer phase, and sequential thermal conductivity and reductive gas detectors allowed good sensitivity for He, Ne, H2, N2, O2, CO, CH4, CO2, and N2O. Within 4 days of immersion in groundwater, samplers initially filled with either He or air attained the same and constant gas composition at an Oak Ridge, Tennessee, site heavily impacted by uranium, acidity, and nitrate. Between June 2006 and July 2007, 12 permanent groundwater wells were used to test the passive samplers in groundwater contaminated by a group of four closed radioactive wastewater seepage ponds; over a thousand passive gas samples from these wells averaged 56% CO2, 32.4% N2, 2.5% O2, 2.5% N2O, 0.20% CH4, 0.096% H2, and 0.023% CO with an average recovery of 95 14% of the injected gas volume

Dynamics of submarine groundwater discharge and associated fluxes of dissolved nutrients, carbon, and trace gases to the coastal zone (Okatee River estuary, South Carolina)

Science.gov (United States)

Porubsky, W.P.; Weston, N.B.; Moore, W.S.; Ruppel, C.; Joye, S.B.

2014-01-01

Multiple techniques, including thermal infrared aerial remote sensing, geophysical and geological data, geochemical characterization and radium isotopes, were used to evaluate the role of groundwater as a source of dissolved nutrients, carbon, and trace gases to the Okatee River estuary, South Carolina. Thermal infrared aerial remote sensing surveys illustrated the presence of multiple submarine groundwater discharge sites in Okatee headwaters. Significant relationships were observed between groundwater geochemical constituents and 226Ra activity in groundwater with higher 226Ra activity correlated to higher concentrations of organics, dissolved inorganic carbon, nutrients, and trace gases to the Okatee system. A system-level radium mass balance confirmed a substantial submarine groundwater discharge contribution of these constituents to the Okatee River. Diffusive benthic flux measurements and potential denitrification rate assays tracked the fate of constituents in creek bank sediments. Diffusive benthic fluxes were substantially lower than calculated radium-based submarine groundwater discharge inputs, showing that advection of groundwater-derived nutrients dominated fluxes in the system. While a considerable potential for denitrification in tidal creek bank sediments was noted, in situ denitrification rates were nitrate-limited, making intertidal sediments an inefficient nitrogen sink in this system. Groundwater geochemical data indicated significant differences in groundwater chemical composition and radium activity ratios between the eastern and western sides of the river; these likely arose from the distinct hydrological regimes observed in each area. Groundwater from the western side of the Okatee headwaters was characterized by higher concentrations of dissolved organic and inorganic carbon, dissolved organic nitrogen, inorganic nutrients and reduced metabolites and trace gases, i.e. methane and nitrous oxide, than groundwater from the eastern side

Recharge processes and vertical transfer investigated through long-term monitoring of dissolved gases in shallow groundwater

Science.gov (United States)

de Montety, V.; Aquilina, L.; Labasque, T.; Chatton, E.; Fovet, O.; Ruiz, L.; Fourré, E.; de Dreuzy, J. R.

2018-05-01

We investigated temporal variations and vertical evolution of dissolved gaseous tracers (CFC-11, CFC-12, SF6, and noble gases), as well as 3H/3He ratio to determine groundwater recharge processes of a shallow unconfined, hard-rock aquifer in an agricultural catchment. We sampled dissolved gas concentration at 4 locations along the hillslope of a small experimental watershed, over 6 hydrological years, between 2 and 6 times per years, for a total of 20 field campaigns. We collected groundwater samples in the fluctuation zone and the permanently saturated zone using piezometers from 5 to 20 m deep. The purpose of this work is i) to assess the benefits of using gaseous tracers like CFCs and SF6 to study very young groundwater with flows suspected to be heterogeneous and variable in time, ii) to characterize the processes that control dissolved gas concentrations in groundwater during the recharge of the aquifer, and iii) to understand the evolution of recharge flow processes by repeated measurement campaigns, taking advantage of a long monitoring in a site devoted to recharge processes investigation. Gas tracer profiles are compared at different location of the catchment and for different hydrologic conditions. In addition, we compare results from CFCs and 3H/3He analysis to define the flow model that best explains tracer concentrations. Then we discuss the influence of recharge events on tracer concentrations and residence time and propose a temporal evolution of residence times for the unsaturated zone and the permanently saturated zone. These results are used to gain a better understanding of the conceptual model of the catchment and flow processes especially during recharge events.

Effect of TCE concentration and dissolved groundwater solutes on NZVI-promoted TCE dechlorination and H2 evolution.

Science.gov (United States)

Liu, Yueqiang; Phenrat, Tanapon; Lowry, Gregory V

2007-11-15

Nanoscale zero-valent iron (NZVI) is used to remediate contaminated groundwater plumes and contaminant source zones. The target contaminant concentration and groundwater solutes (NO3-, Cl-, HCO3-, SO4(2-), and HPO4(2-)) should affect the NZVI longevity and reactivity with target contaminants, but these effects are not well understood. This study evaluates the effect of trichloroethylene (TCE) concentration and common dissolved groundwater solutes on the rates of NZVI-promoted TCE dechlorination and H2 evolution in batch reactors. Both model systems and real groundwater are evaluated. The TCE reaction rate constant was unaffected by TCE concentration for [TCE] TCE concentration up to water saturation (8.4 mM). For [TCE] > or = 0.46 mM, acetylene formation increased, and the total amount of H2 evolved at the end of the particle reactive lifetime decreased with increasing [TCE], indicating a higher Fe0 utilization efficiency for TCE dechlorination. Common groundwater anions (5mN) had a minor effect on H2 evolution but inhibited TCE reduction up to 7-fold in increasing order of Cl- TCE reduction but increased acetylene production and decreased H2 evolution. NO3- present at > 3 mM slowed TCE dechlorination due to surface passivation. NO3- present at 5 mM stopped TCE dechlorination and H2 evolution after 3 days. Dissolved solutes accounted for the observed decrease of NZVI reactivity for TCE dechlorination in natural groundwater when the total organic content was small (< 1 mg/L).

Paleotemperatures derived from noble gases dissolved in groundwater and in relation to soil temperature

International Nuclear Information System (INIS)

Stute, M.; Sonntag, C.

1992-01-01

Measurements of He, Ne, Ar, Kr and Xe dissolved in groundwater at two sites (Bocholt, Germany, and the Great Hungarian Plain) were taken to prove the reliability of noble gas temperatures as indicators of paleotemperatures. Noble gas temperatures of groundwater of Holocene age were found to reflect the annual mean soil temperature in the recharge are with an accuracy close to the precision of measurement (1σ approx. ±0.5 deg. C). Noble gas temperature data demonstrate the influence of vegetation cover on the soil temperature in the infiltration area. Groundwater formed in forests at the Bocholt site shows noble gas temperatures that are 2.2 deg. C lower than the groundwater formed in fields or meadows. The temperature data obtained from groundwater of the Great Hungarian Plain for the last glaciation are ≥ 8.6 deg. C lower than data from recent groundwater for maximum glaciation (approx. 18,000 years ago) and 4.7 ± 1 deg. C lower for the preceding interstadial (approx. 28,000-35,000 years ago). These data permit independent reconstruction of paleoclimatic conditions. (author). 19 refs, 3 figs, 1 tab

Natural spatial and temporal variations in groundwater chemistry in fractured, sedimentary rocks: scale and implications for solute transport

International Nuclear Information System (INIS)

Hoven, Stephen J. van der; Kip Solomon, D.; Moline, Gerilynn R.

2005-01-01

Natural tracers (major ions, δ 18 O, and O 2 ) were monitored to evaluate groundwater flow and transport to a depth of 20 m below the surface in fractured sedimentary (primarily shale and limestone) rocks. Large temporal variations in these tracers were noted in the soil zone and the saprolite, and are driven primarily by individual storm events. During nonstorm periods, an upward flow brings water with high TDS, constant δ 18 O, and low dissolved O 2 to the water table. During storm events, low TDS, variable δ 18 O, and high dissolved O 2 water recharges through the unsaturated zone. These oscillating signals are rapidly transmitted along fracture pathways in the saprolite, with changes occurring on spatial scales of several meters and on a time scale of hours. The variations decreased markedly below the boundary between the saprolite and less weathered bedrock. Variations in the bedrock units occurred on time scales of days and spatial scales of at least 20 m. The oscillations of chemical conditions in the shallow groundwater are hypothesized to have significant implications for solute transport. Solutes and colloids that adsorb onto aquifer solids can be released into solution by decreases in ionic strength and pH. The decreases in ionic strength also cause thermodynamic undersaturation of the groundwater with respect to some mineral species and may result in mineral dissolution. Redox conditions are also changing and may result in mineral dissolution/precipitation. The net result of these chemical variations is episodic transport of a wide range of dissolved solutes or suspended particles, a phenomenon rarely considered in contaminant transport studies

Dissolved organic matter composition of winter flow in the Yukon River basin: Implications of permafrost thaw and increased groundwater discharge

Science.gov (United States)

O'Donnell, Jonathan A.; Aiken, George R.; Walvoord, Michelle Ann; Butler, Kenna D.

2012-01-01

Groundwater discharge to rivers has increased in recent decades across the circumpolar region and has been attributed to thawing permafrost in arctic and subarctic watersheds. Permafrost-driven changes in groundwater discharge will alter the flux of dissolved organic carbon (DOC) in rivers, yet little is known about the chemical composition and reactivity of dissolved organic matter (DOM) of groundwater in permafrost settings. Here, we characterize DOM composition of winter flow in 60 rivers and streams of the Yukon River basin to evaluate the biogeochemical consequences of enhanced groundwater discharge associated with permafrost thaw. DOC concentration of winter flow averaged 3.9 ± 0.5 mg C L−1, yet was highly variable across basins (ranging from 20 mg C L−1). In comparison to the summer-autumn period, DOM composition of winter flow had lower aromaticity (as indicated by specific ultraviolet absorbance at 254 nm, or SUVA254), lower hydrophobic acid content, and a higher proportion of hydrophilic compounds (HPI). Fluorescence spectroscopy and parallel factor analysis indicated enrichment of protein-like fluorophores in some, but not all, winter flow samples. The ratio of DOC to dissolved organic nitrogen, an indicator of DOM biodegradability, was positively correlated with SUVA254 and negatively correlated with the percentage of protein-like compounds. Using a simple two-pool mixing model, we evaluate possible changes in DOM during the summer-autumn period across a range of conditions reflecting possible increases in groundwater discharge. Across three watersheds, we consistently observed decreases in DOC concentration and SUVA254 and increases in HPI with increasing groundwater discharge. Spatial patterns in DOM composition of winter flow appear to reflect differences in the relative contributions of groundwater from suprapermafrost and subpermafrost aquifers across watersheds. Our findings call for more explicit consideration of DOC loss and stabilization

Groundwater and surface-water interaction, water quality, and processes affecting loads of dissolved solids, selenium, and uranium in Fountain Creek near Pueblo, Colorado, 2012–2014

Science.gov (United States)

Arnold, L. Rick; Ortiz, Roderick F.; Brown, Christopher R.; Watts, Kenneth R.

2016-11-28

In 2012, the U.S. Geological Survey, in cooperation with the Arkansas River Basin Regional Resource Planning Group, initiated a study of groundwater and surface-water interaction, water quality, and loading of dissolved solids, selenium, and uranium to Fountain Creek near Pueblo, Colorado, to improve understanding of sources and processes affecting loading of these constituents to streams in the Arkansas River Basin. Fourteen monitoring wells were installed in a series of three transects across Fountain Creek near Pueblo, and temporary streamgages were established at each transect to facilitate data collection for the study. Groundwater and surface-water interaction was characterized by using hydrogeologic mapping, groundwater and stream-surface levels, groundwater and stream temperatures, vertical hydraulic-head gradients and ratios of oxygen and hydrogen isotopes in the hyporheic zone, and streamflow mass-balance measurements. Water quality was characterized by collecting periodic samples from groundwater, surface water, and the hyporheic zone for analysis of dissolved solids, selenium, uranium, and other selected constituents and by evaluating the oxidation-reduction condition for each groundwater sample under different hydrologic conditions throughout the study period. Groundwater loads to Fountain Creek and in-stream loads were computed for the study area, and processes affecting loads of dissolved solids, selenium, and uranium were evaluated on the basis of geology, geochemical conditions, land and water use, and evapoconcentration.During the study period, the groundwater-flow system generally contributed flow to Fountain Creek and its hyporheic zone (as a single system) except for the reach between the north and middle transects. However, the direction of flow between the stream, the hyporheic zone, and the near-stream aquifer was variable in response to streamflow and stage. During periods of low streamflow, Fountain Creek generally gained flow from

Occurrences of dissolved trace metals (Cu, Cd, and Mn) in the Pearl River Estuary (China), a large river-groundwater-estuary system

Science.gov (United States)

Wang, Deli; Lin, Wenfang; Yang, Xiqian; Zhai, Weidong; Dai, Minhan; Arthur Chen, Chen-Tung

2012-12-01

This study for the first time examined dissolved metals (Cu, Cd, and Mn) together with dissolved oxygen and carbonate system in the whole Pearl River Estuary system, from the upper rivers to the groundwater discharges until the estuarine zone, and explored their potential impacts in the adjacent northern South China Sea (SCS) during May-August 2009. This river-groundwater-estuary system was generally characterized by low dissolved metal levels as a whole, whilst subject to severe perturbations locally. In particular, higher dissolved Cu and Cd occurred in the North River (as high as 60 nmol/L of Cu and 0.99 nmol/L of Cd), as a result of an anthropogenic source from mining activities there. Dissolved Cu levels were elevated in the upper estuary near the city of Guangzhou (Cu: ˜40 nmol/L), which could be attributable to sewage and industrial effluent discharges there. Elevated dissolved metal levels (Cu: ˜20-40 nmol/L; Cd: ˜0.2-0.8 nmol/L) also occurred in the groundwaters and parts of the middle and lower estuaries, which could be attributable to a series of geochemical reactions, e.g., chloride-induced desorption from the suspended sediments, oxidation of metal sulfides, and the partial dissolution of minerals. The high river discharge during our sampling period (May-August 2009) significantly diluted anthropogenic signals in the estuarine mixing zone. Of particular note was the high river discharge (which may reach 18.5 times as high as in the dry season) that transported anthropogenic signals (as indicated by dissolved Cu and Cd) into the adjacent shelf waters of the northern SCS, and might have led to the usually high phytoplankton productivity there (chlorophyll-a value >10 μg/L).

The origin and isotopic composition of dissolved sulfide in groundwater from carbonate aquifers in Florida and Texas

International Nuclear Information System (INIS)

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

1981-01-01

The delta 34 S values of dissolved sulfide and the sulfur isotope fractionations between dissolved sulfide and sulfate species in Floridan ground water generally correlate with dissolved sulfate concentrations which are related to flow patterns and residence time within the aquifer. The dissolved sulfide derives from the slow in situ biogenic reduction of sulfate dissolved from sedimentary gypsum in the aquifer. In areas where the water is oldest, the dissolved sulfide has apparently attained isotopic equilibrium with the dissolved sulfate at the temperature of the system. This approach to equilibrium reflects an extremely slow reduction rate of the dissolved sulfate by bacteria; this slow rate probably results from very low concentrations of organic matter in the aquifer. In the reducing part of the Edwards aquifer, Texas, there is a general down-gradient increase in both dissolved sulfide and sulfate concentrations, but neither the delta 34 S values of sulfide nor the sulfide-sulfate isotope fractionation correlates with the ground-water flow pattern. The dissolved sulfide species appear to be derived primarily from biogenic reduction of sulfate ions whose source is gypsum dissolution although upgradient diffusion of H 2 S gas from deeper oil field brines may be important in places. (author)

Distribution and origin of dissolved methane, ethane and propane in shallow groundwater of Lower Saxony, Germany

International Nuclear Information System (INIS)

Schloemer, S.; Elbracht, J.; Blumenberg, M.; Illing, C.J.

2016-01-01

More than 90% of Germany's domestic natural gas production and reserves are located in Lower Saxony, North Germany. Recently, research has been intensified with respect to unconventional shale gas, revealing a large additional resource potential in northern Germany. However, many concerns arise within the general public and government/political institutions over potential groundwater contamination from additional gas wells through hydraulic fracturing operations. In order to determine the naturally occurring background methane concentrations, ∼1000 groundwater wells, covering ∼48 000 km 2 , have been sampled and subsequently analyzed for dissolved methane, ethane and propane and the isotopic composition of methane (δ 13 C). Dissolved methane concentrations cover a range of ∼7 orders of magnitude between the limit of quantification at ∼20 nl/l and 60 ml/l. The majority of groundwater wells exhibit low concentrations (<1 μl/l), a small number of samples (65) reveal concentration in the range >10 ml/l. In 27% of all samples ethane and in 8% ethane and propane was detected. The median concentration of both components is generally very low (ethane 50 nl/l, propane 23 nl/l). Concentrations reveal a bimodal distribution of the dissolved gas, which might mirror a regional trend due to different hydrogeological settings. The isotopic composition of methane is normally distributed (mean ∼ −70‰ vs PDB), but shows a large variation between −110‰ and +20‰. Samples with δ 13 C values lower than −55‰ vs PDB (66%) are indicative for methanogenic biogenic processes. 5% of the samples are unusually enriched in 13 C (≥25‰ vs PDB) and can best be explained by microbial methane oxidation. According to a standard diagnostic diagram based on methane δ 13 C values and the ratio of methane over the sum over ethane plus propane (“Bernard”-diagram) less than 4% of the samples plot into the diagnostic field of typical thermogenic natural

The isotopic chemical and dissolved gas concentrations in groundwater near Venterstad, Cape Province

International Nuclear Information System (INIS)

Vogel, J.C.; Talma, A.S.; Heaton, T.H.E.

1980-01-01

Groundwater was collected for a multi parameter investigation from 27 boreholes within a radius of 120 km from Venterstad (Cape Province). The samples were analysed for the isotopes carbon-14, carbon-13, oxygen-18, tritium and radon-222, for the dissolved gases nitrogen, oxygen, argon, methane and helium and for the major ionic species. These data, with those collected during previous investigations of the flooding of the Orange Fish tunnel, are used to discuss the geohydrology of the area. Three water types of different origin were delineated

Hydro-ecological controls on dissolved carbon dynamics in groundwater and export to streams in a temperate pine forest

Science.gov (United States)

Deirmendjian, Loris; Loustau, Denis; Augusto, Laurent; Lafont, Sébastien; Chipeaux, Christophe; Poirier, Dominique; Abril, Gwenaël

2018-02-01

We studied the export of dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC) from forested shallow groundwater to first-order streams, based on groundwater and surface water sampling and hydrological data. The selected watershed was particularly convenient for such study, with a very low slope, with pine forest growing on sandy permeable podzol and with hydrology occurring exclusively through drainage of shallow groundwater (no surface runoff). A forest plot was instrumented for continuous eddy covariance measurements of precipitation, evapotranspiration, and net ecosystem exchanges of sensible and latent heat fluxes as well as CO2 fluxes. Shallow groundwater was sampled with three piezometers located in different plots, and surface waters were sampled in six first-order streams; river discharge and drainage were modeled based on four gauging stations. On a monthly basis and on the plot scale, we found a good consistency between precipitation on the one hand and the sum of evapotranspiration, shallow groundwater storage and drainage on the other hand. DOC and DIC stocks in groundwater and exports to first-order streams varied drastically during the hydrological cycle, in relation with water table depth and amplitude. In the groundwater, DOC concentrations were maximal in winter when the water table reached the superficial organic-rich layer of the soil. In contrast, DIC (in majority excess CO2) in groundwater showed maximum concentrations at low water table during late summer, concomitant with heterotrophic conditions of the forest plot. Our data also suggest that a large part of the DOC mobilized at high water table was mineralized to DIC during the following months within the groundwater itself. In first-order streams, DOC and DIC followed an opposed seasonal trend similar to groundwater but with lower concentrations. On an annual basis, leaching of carbon to streams occurred as DIC and DOC in similar proportion, but DOC export occurred in

Hydro-ecological controls on dissolved carbon dynamics in groundwater and export to streams in a temperate pine forest

Directory of Open Access Journals (Sweden)

L. Deirmendjian

2018-02-01

Full Text Available We studied the export of dissolved inorganic carbon (DIC and dissolved organic carbon (DOC from forested shallow groundwater to first-order streams, based on groundwater and surface water sampling and hydrological data. The selected watershed was particularly convenient for such study, with a very low slope, with pine forest growing on sandy permeable podzol and with hydrology occurring exclusively through drainage of shallow groundwater (no surface runoff. A forest plot was instrumented for continuous eddy covariance measurements of precipitation, evapotranspiration, and net ecosystem exchanges of sensible and latent heat fluxes as well as CO2 fluxes. Shallow groundwater was sampled with three piezometers located in different plots, and surface waters were sampled in six first-order streams; river discharge and drainage were modeled based on four gauging stations. On a monthly basis and on the plot scale, we found a good consistency between precipitation on the one hand and the sum of evapotranspiration, shallow groundwater storage and drainage on the other hand. DOC and DIC stocks in groundwater and exports to first-order streams varied drastically during the hydrological cycle, in relation with water table depth and amplitude. In the groundwater, DOC concentrations were maximal in winter when the water table reached the superficial organic-rich layer of the soil. In contrast, DIC (in majority excess CO2 in groundwater showed maximum concentrations at low water table during late summer, concomitant with heterotrophic conditions of the forest plot. Our data also suggest that a large part of the DOC mobilized at high water table was mineralized to DIC during the following months within the groundwater itself. In first-order streams, DOC and DIC followed an opposed seasonal trend similar to groundwater but with lower concentrations. On an annual basis, leaching of carbon to streams occurred as DIC and DOC in similar proportion, but DOC export

Dissolution Dominating Calcification Process in Polar Pteropods Close to the Point of Aragonite Undersaturation

Science.gov (United States)

Bednaršek, Nina; Tarling, Geraint A.; Bakker, Dorothee C. E.; Fielding, Sophie; Feely, Richard A.

2014-01-01

Thecosome pteropods are abundant upper-ocean zooplankton that build aragonite shells. Ocean acidification results in the lowering of aragonite saturation levels in the surface layers, and several incubation studies have shown that rates of calcification in these organisms decrease as a result. This study provides a weight-specific net calcification rate function for thecosome pteropods that includes both rates of dissolution and calcification over a range of plausible future aragonite saturation states (Ωar). We measured gross dissolution in the pteropod Limacina helicina antarctica in the Scotia Sea (Southern Ocean) by incubating living specimens across a range of aragonite saturation states for a maximum of 14 days. Specimens started dissolving almost immediately upon exposure to undersaturated conditions (Ωar∼0.8), losing 1.4% of shell mass per day. The observed rate of gross dissolution was different from that predicted by rate law kinetics of aragonite dissolution, in being higher at Ωar levels slightly above 1 and lower at Ωar levels of between 1 and 0.8. This indicates that shell mass is affected by even transitional levels of saturation, but there is, nevertheless, some partial means of protection for shells when in undersaturated conditions. A function for gross dissolution against Ωar derived from the present observations was compared to a function for gross calcification derived by a different study, and showed that dissolution became the dominating process even at Ωar levels close to 1, with net shell growth ceasing at an Ωar of 1.03. Gross dissolution increasingly dominated net change in shell mass as saturation levels decreased below 1. As well as influencing their viability, such dissolution of pteropod shells in the surface layers will result in slower sinking velocities and decreased carbon and carbonate fluxes to the deep ocean. PMID:25285916

Effect of phytoremediation on concentrations of benzene, toluene, naphthalene, and dissolved oxygen in groundwater at a former manufactured gas plant site, Charleston, South Carolina, USA, 1998–2014

Science.gov (United States)

Landmeyer, James E.; Effinger, Thomas N.

2016-01-01

Concentrations of benzene, toluene, naphthalene, and dissolved oxygen in groundwater at a former manufactured gas plant site near Charleston, South Carolina, USA, have been monitored since the installation of a phytoremediation system of hybrid poplar trees in 1998. Between 2000 and 2014, the concentrations of benzene, toluene, and naphthalene (BT&N) in groundwater in the planted area have decreased. For example, in the monitoring well containing the highest concentrations of BT&N, benzene concentrations decreased from 10,200 µg/L to less than 4000 µg/L, toluene concentrations decreased from 2420 µg/L to less than 20 µg/L, and naphthalene concentrations decreased from 6840 µg/L to less than 3000 µg/L. Concentrations of BT&N in groundwater in all wells were observed to be lower during the summer months relative to the winter months of a particular year during the first few years after installing the phytoremediation system, most likely due to increased transpiration and contaminant uptake by the hybrid poplar trees during the warm summer months; this pathway of uptake by trees was confirmed by the detection of benzene, toluene, and naphthalene in trees during sampling events in 2002, and later in the study in 2012. These data suggest that the phytoremediation system affects the groundwater contaminants on a seasonal basis and, over multiple years, has resulted in a cumulative decrease in dissolved-phase contaminant concentrations in groundwater. The removal of dissolved organic contaminants from the aquifer has resulted in a lower demand on dissolved oxygen supplied by recharge and, as a result, the redox status of the groundwater has changed from anoxic to oxic conditions. This study provides much needed information for water managers and other scientists on the viability of the long-term effectiveness of phytoremediation in decreasing groundwater contaminants and increasing dissolved oxygen at sites contaminated by benzene, toluene, and naphthalene.

Dissolved gases

International Nuclear Information System (INIS)

Heaton, T.H.E.

1981-01-01

The concentrations of gaseous nitrogen, argon, oxygen and helium dissolved in groundwater are often different from their concentrations in rain and surface waters. These differences reflect changes in the gas content occurring after rain or surface water, having infiltrated into the ground, become isolated from equilibrium contact with the atmosphere. A study of these changes can give insight into the origin and subsequent subsurface history of groundwater. Nitrogen and argon concentrations for many groundwaters in southern Africa indicate that excess air is added to water during infiltration. The amount of excess air is believed to reflect the physical structure of the unsaturated zone and the climate of the recharge area. Since nitrogen and argon are essentially conservative in many aquifer environments in South Africa, their concentrations can be used in distinguishing grondwaters of different recharge origins. In some areas the high helium content of the groundwater suggests that much of the helium is derived through migration from a source outside (e.g. below) the aquifer itself. Radiogenic helium concentrations nevertheless show, in two artesian aquifers, a close linear relationship to the radiocarbon age of the groundwater. This indicates a uniformity in the factors responsible for the accumulation of helium, and suggests that in these circumstances helium data can be used to give information on the age of very old groundwater. In some groundwater dissolved oxygen concentrations are found to decrease with increasing groundwater age. Whilst the rate of decrease may be very different for different aquifers, the field measurement of oxygen may be useful in preliminary surveys directed toward the location of recharge areas

The source and behavior of iodine dissolving in groundwater in the Mobara gas field, Japan

Energy Technology Data Exchange (ETDEWEB)

Kamei, Gento [Japan Nuclear Cycle Development Inst., Tokai, Ibaraki (Japan). Tokai Works

2002-06-01

The groundwater of the Mobara gas-field in Boso peninsula, eastern Japan, contains considerable amount, around 100 mg/L, of iodine besides dissolved methane. Twelve groundwater samples from gas-producing wells to the aquifer within the Kazusa Group in Mobara and Naruto districts have been analyzed for iodine, pH, Eh, HCO{sub 3}{sup -}, NH{sub 4}{sup +}, SiO{sub 2}(aq), {delta}D, {delta}{sup 18}O, {delta}{sup 13}C{sub CH4} and seventeen elements. There is a good correlation between the concentrations of the dissolved elements to those in marine algae. The principal source of the iodine is believed to be algae buried in the sediments and the iodine has been discharged to the porefluid during decomposition of the tissue. The molar ratio of I{sup -}/Cl{sup -} in the groundwater increases from 1.0 x 10{sup 3} to 2.2 x 10{sup 3} with changing the depth from 2000 to 1000 meters below the surface and turns to decrease from 2.2 x 10{sup 3} to 1.8 x 10{sup 3} with going up from 1000 to 500 meters. This tendency may be caused by the variation of buried organisms due to changing the sedimentary environment. The observed variation in the ratio indicates that the iodine discharged in the pore fluid did not migrate significantly after the deposition of the formation. This paper can be regarded as an English version of Japanese article written by Kamei, which was published on the 'Shigen Chishitsu (Resource Geology)' 51(2)145-151(2000). (author)

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

The hydrochemistry of groundwater in rural communities within the Tema District, Ghana.

Science.gov (United States)

Fianko, Joseph Richmond; Nartey, Vincent K; Donkor, Augustine

2010-09-01

A detailed study has been carried out on groundwater in rural communities in the Tema District of the Greater Accra region of Ghana to establish the hydrochemistry and identify the various sources of contaminants as well assess the physical and chemical quality of the groundwater to ascertain their wholesomeness and the health impacts of the groundwater on the communities. The groundwater was found to vary considerably in terms of chemical and physical properties. Generally, the water was mildly acidic (pH 4.3-7.4), brackish to fresh, and undersaturated with respect to gypsum and halite. The majority of groundwater clustered toward Ca-Mg-SO(4) and Na-Cl facies. About 70% of boreholes sampled have elevated levels of NO(3)(-) -N, Cl(-), and SO(4)(2-) emanating from anthropogenic activities.

Attempt of groundwater dating using the drilled rock core. 1. Development of the rock sampling method for measurement of noble gases dissolved in interstitial water in rock

International Nuclear Information System (INIS)

Mahara, Yasunori

2002-01-01

Groundwater dating in low permeable rock is very difficult and impracticable, because we take a very long time to collect groundwater sample in a borehole and have to invest much fund in production of the in-situ groundwater sampler and in operation of it. If we can directly measure noble gases dissolved in interstitial groundwater in rock core, we have a big merit to estimate groundwater resident time easy. In this study, we designed and produced a high vacuum container to let dissolved noble gases diffuse until reaching in equilibrium, and we made a handling manual of the rock core into the container and a procedure to vacuum out air from the sealed container. We compared data sets of noble gas concentration obtained from rock cores and groundwater sample collected from boreholes in-situ. The measured rocks are pumice-tuff rock, mud rock and hornfels, which have their permeabilities of 10 -6 cm/s, 10 -9 cm/s and 10 -11 cm/s, respectively. Consequently, we evaluated the rock core method is better than the in-situ groundwater sampling method for low permeable rock. (author)

SITE demonstration of the Dynaphore/Forager Sponge technology to remove dissolved metals from contaminated groundwater

Energy Technology Data Exchange (ETDEWEB)

Esposito, C.R. [Environmental Protection Agency, Edison, NJ (United States); Vaccaro, G. [Science Applications International Corp., Hackensack, NJ (United States)

1995-10-01

A Superfund Innovative Technology Evaluation (SITE) demonstration was conducted of the Dynaphore/Forager Sponge technology during the week of April 3, 1994 at the N.L. Industries Superfund Site in Pedricktown, New Jersey. The Forager Sponge is an open-celled cellulose sponge incorporating an amine-containing chelating polymer that selectively absorbs dissolved heavy metals in both cationic and anionic states. This technology is a volume reduction technology in which heavy metal contaminants from an aqueous medium are concentrated into a smaller volume for facilitated disposal. The developer states that the technology can be used to remove heavy metals from a wide variety of aqueous media, such as groundwater, surface waters and process waters. The sponge matrix can be directly disposed, or regenerated with chemical solutions. For this demonstration the sponge was set up as a mobile pump-and-treat system which treated groundwater contaminated with heavy metals. The demonstration focused on the system`s ability to remove lead, cadmium, chromium and copper from the contaminated groundwater over a continuous 72-hour test. The removal of heavy metals proceeded in the presence of significantly higher concentrations of innocuous cations such as calcium, magnesium, sodium, potassium and aluminum.

δ34S and δ18O of dissolved sulfate as biotic tracer of biogeochemical influences on arsenic mobilization in groundwater in the Hetao Plain, Inner Mongolia, China.

Science.gov (United States)

Li, M D; Wang, Y X; Li, P; Deng, Y M; Xie, X J

2014-12-01

Environmental isotopology of sulfur and oxygen of dissolved sulfate in groundwater was conducted in the Hetao Plain, northwestern China, aiming to better understand the processes controlling arsenic mobilization in arsenic-rich aqueous systems. A total of 22 groundwater samples were collected from domestic wells in the Hetao Plain. Arsenic concentrations ranged from 11.0 to 388 μg/L. The δ(34)S-SO4 and δ(18)O-SO4 values of dissolved sulfate covered a range from +1.48 to +22.4‰ and +8.17‰ to +14.8‰ in groundwater, respectively. The wide range of δ(34)S-SO4 values reflected either an input of different sources of sulfate, such as gypsum dissolution and fertilizer application, or a modification from biogeochemical process of bacterial sulfate reduction. The positive correlation between δ(34)S-SO4 and arsenic concentrations suggested that bacteria mediated processes played an important role in the mobilization of arsenic. The δ(18)O-SO4 values correlated non-linearly with δ(34)S-SO4, but within a relatively narrow range (+8.17 to +14.8‰), implying that complexities inherent in the sulfate-oxygen (O-SO4(2-)) origins, for instance, water-derived oxygen (O-H2O), molecular oxygen (O-O2) and isotope exchanging with dissolved oxides, are accounted for oxygen isotope composition of dissolved sulfate in groundwater in the Hetao Plain.

Hydrogeochemical and Isotopic Study of Groundwaters from the Gañuelas-Mazarrón Tertiary Basin (Murcia, Spain)

International Nuclear Information System (INIS)

Rodrigo-Naharro, J.; Delgado, A.; Clemente-Jul, C.; Pérez del Villar, L.

2015-01-01

The hydrogeochemical characterisation of groundwaters from the Gañuelas-Mazarrón Tertiary Basin included: i) to establish the different hydrofacies present in the basin; ii) to perform a cluster analysis in order to reduce the water samples, grouping them according to their physicochemical characteristics; and iii) to determine the most relevant ion ratios for understanding the water/ rock interaction processes that regulate the main features and evolution of groundwaters. It has also been discussed the origin and concentration of the minor and trace elements to evaluate the capability of groundwaters to transport heavy elements, toxic or innocuous, towards the surface, thus determining their suitability for human consumption. Besides, the hydrogeochemical modeling has allowed determining the degree of groundwaters saturation with respect to the most representative mineral phases of the aquifers, which, in turn, it has been used to calculate their theoretical temperature in depth. The isotopic characterisation of groundwaters has included the isotopic signatures of the stable (δ18O, δ2H, δ13C-DIC, δ34S(SO4 2-) and δ18O(SO4 2-)) and radioactive (238U, 234U and 226Ra) isotopes. The first have been used to distinguish the groundwaters origin, as well as the origin of the dissolved C and SO4 2-. The radioactive isotopes have been used to determine the water/rock interaction processes involving 238U radioactive series, as well as to explain the origin of the dissolved 222Rn in groundwaters. The most important hydrogeochemical results obtained from groundwaters are: i) a large variety of hydrofacies is represented in them, corroborated by the cluster analysis; ii) they are not suitable for human consumption; iii) they have remained, apparently, over-saturated with respect to calcite and aragonite, and under-saturated with respect to gypsum, anhydrite and halite, over time; iv) they present theoretical temperatures in depth much higher than in the surface; v) they

Groundwater-quality characteristics for the Wyoming Groundwater-Quality Monitoring Network, November 2009 through September 2012

Science.gov (United States)

Boughton, Gregory K.

2014-01-01

Groundwater samples were collected from 146 shallow (less than or equal to 500 feet deep) wells for the Wyoming Groundwater-Quality Monitoring Network, from November 2009 through September 2012. Groundwater samples were analyzed for physical characteristics, major ions and dissolved solids, trace elements, nutrients and dissolved organic carbon, uranium, stable isotopes of hydrogen and oxygen, volatile organic compounds, and coliform bacteria. Selected samples also were analyzed for gross alpha radioactivity, gross beta radioactivity, radon, tritium, gasoline range organics, diesel range organics, dissolved hydrocarbon gases (methane, ethene, and ethane), and wastewater compounds. Water-quality measurements and concentrations in some samples exceeded numerous U.S. Environmental Protection Agency (EPA) drinking water standards. Physical characteristics and constituents that exceeded EPA Maximum Contaminant Levels (MCLs) in some samples were arsenic, selenium, nitrite, nitrate, gross alpha activity, and uranium. Total coliforms and Escherichia coli in some samples exceeded EPA Maximum Contaminant Level Goals. Measurements of pH and turbidity and concentrations of chloride, sulfate, fluoride, dissolved solids, aluminum, iron, and manganese exceeded EPA Secondary Maximum Contaminant Levels in some samples. Radon concentrations in some samples exceeded the alternative MCL proposed by the EPA. Molybdenum and boron concentrations in some samples exceeded EPA Health Advisory Levels. Water-quality measurements and concentrations also exceeded numerous Wyoming Department of Environmental Quality (WDEQ) groundwater standards. Physical characteristics and constituents that exceeded WDEQ Class I domestic groundwater standards in some samples were measurements of pH and concentrations of chloride, sulfate, dissolved solids, iron, manganese, boron, selenium, nitrite, and nitrate. Measurements of pH and concentrations of chloride, sulfate, dissolved solids, aluminum, iron

Hydrochemistry of urban groundwater, Seoul, Korea: the impact of subway tunnels on groundwater quality.

Science.gov (United States)

Chae, Gi-Tak; Yun, Seong-Taek; Choi, Byoung-Young; Yu, Soon-Young; Jo, Ho-Young; Mayer, Bernhard; Kim, Yun-Jong; Lee, Jin-Yong

2008-10-23

Hydrogeologic and hydrochemical data for subway tunnel seepage waters in Seoul (Republic of Korea) were examined to understand the effect of underground tunnels on the degradation of urban groundwater. A very large quantity of groundwater (up to 63 million m3 year(-1)) is discharged into subway tunnels with a total length of 287 km, resulting in a significant drop of the local groundwater table and the abandonment of groundwater wells. For the tunnel seepage water samples (n = 72) collected from 43 subway stations, at least one parameter among pathogenic microbes (total coliform, heterotrophic bacteria), dissolved Mn and Fe, NH4+, NO3(-), turbidity, and color exceeded the Korean Drinking Water Standards. Locally, tunnel seepage water was enriched in dissolved Mn (avg. 0.70 mg L(-1), max. 5.58 mg L(-1)), in addition to dissolved Fe, NH4+, and pathogenic microbes, likely due to significant inflow of sewage water from broken or leaking sewer pipes. Geochemical modeling of redox reactions was conducted to simulate the characteristic hydrochemistry of subway tunnel seepage. The results show that variations in the reducing conditions occur in urban groundwater, dependent upon the amount of organic matter-rich municipal sewage contaminating the aquifer. The organic matter facilitates the reduction and dissolution of Mn- and Fe-bearing solids in aquifers and/or tunnel construction materials, resulting in the successive increase of dissolved Mn and Fe. The present study clearly demonstrates that locally significant deterioration of urban groundwater is caused by a series of interlinked hydrogeologic and hydrochemical changes induced by underground tunnels.

Assessing the effect of dissolved organic ligands on mineral dissolution rates: An example from calcite dissolution

International Nuclear Information System (INIS)

DeMaio, T.; Grandstaff, D.E.

1997-01-01

Experiments suggest that dissolved organic ligands may primarily modify mineral dissolution rates by three mechanisms: (1) metal-ligand (M-L) complex formation in solution, which increases the degree of undersaturation, (2) formation of surface M-L complexes that attack the surface, and (3) formation of surface complexes which passivate or protect the surface. Mechanisms (1) and (2) increase the dissolution rate and the third decreases it compared with organic-free solutions. The types and importance of these mechanisms may be assessed from plots of dissolution rate versus degree of undersaturation. To illustrate this technique, calcite, a common repository cementing and vein-filling mineral, was dissolved at pH 7.8 and 22 C in Na-Ca-HCO 3 -Cl solutions with low concentrations of three organic ligands. Low citrate concentrations (50 microM) increased the dissolution rate consistent with mechanism (1). Oxalate decreased the rate, consistent with mechanism (3). Low phthalate concentration (<50 microM) decreased calcite dissolution rates; however, higher concentrations increased the dissolution rates, which became faster than in inorganic solutions. Thus, phthalate exhibits both mechanisms (2) and (3) at different concentrations. In such cases linear extrapolations of dissolution rates from high organic ligand concentrations may not be valid

Dissolved methane in New York groundwater, 1999-2011

Science.gov (United States)

Kappel, William M.; Nystrom, Elizabeth A.

2012-01-01

fracturing in New York, the natural occurrence of methane in the State's aquifers needs to be documented. This brief report presents a compilation of data on dissolved methane concentrations in the groundwater of New York available from the U.S. Geological Survey (USGS) National Water Information System (NWIS) (http://waterdata.usgs.gov/nwis).

Dynamics of dissolved organic carbon (DOC) through stormwater basins designed for groundwater recharge in urban area: Assessment of retention efficiency.

Science.gov (United States)

Mermillod-Blondin, Florian; Simon, Laurent; Maazouzi, Chafik; Foulquier, Arnaud; Delolme, Cécile; Marmonier, Pierre

2015-09-15

Managed aquifer recharge (MAR) has been developed in many countries to limit the risk of urban flooding and compensate for reduced groundwater recharge in urban areas. The environmental performances of MAR systems like infiltration basins depend on the efficiency of soil and vadose zone to retain stormwater-derived contaminants. However, these performances need to be finely evaluated for stormwater-derived dissolved organic matter (DOM) that can affect groundwater quality. Therefore, this study examined the performance of MAR systems to process DOM during its transfer from infiltration basins to an urban aquifer. DOM characteristics (fluorescent spectroscopic properties, biodegradable and refractory fractions of dissolved organic carbon -DOC-, consumption by micro-organisms during incubation in slow filtration sediment columns) were measured in stormwater during its transfer through three infiltration basins during a stormwater event. DOC concentrations sharply decreased from surface to the aquifer for the three MAR sites. This pattern was largely due to the retention of biodegradable DOC which was more than 75% for the three MAR sites, whereas the retention of refractory DOC was more variable and globally less important (from 18% to 61% depending on MAR site). Slow filtration column experiments also showed that DOC retention during stormwater infiltration through soil and vadose zone was mainly due to aerobic microbial consumption of the biodegradable fraction of DOC. In parallel, measurements of DOM characteristics from groundwaters influenced or not by MAR demonstrated that stormwater infiltration increased DOC quantity without affecting its quality (% of biodegradable DOC and relative aromatic carbon content -estimated by SUVA254-). The present study demonstrated that processes occurring in soil and vadose zone of MAR sites were enough efficient to limit DOC fluxes to the aquifer. Nevertheless, the enrichments of DOC concentrations measured in groundwater below

Measurements of the Activity of dissolved H2O in an Andesite Melt

Science.gov (United States)

Moore, G. M.; Touran, J. P.; Pu, X.; Kelley, K. A.; Cottrell, E.; Ghiorso, M. S.

2016-12-01

The large effect of dissolved H2O on the physical and chemical nature of silicate melts, and its role in driving volcanism, is well known and underscores the importance of this volatile component. A complete understanding of the chemical behavior of dissolved H2O in silicate melts requires the quantification of its thermodynamic activity as a function of pressure, temperature, and melt composition, particularly at low H2O contents (i.e. at under-saturated conditions). Knowledge of the activity of H2O in silicate melts at H2O-undersaturated conditions will improve our understanding of hydrous phase equilibria, as well as our models of physical melt properties. Measurement of the activity of any silicate melt component, much less that of a volatile component such as H2O, is a difficult experimental task however. By using a modified double capsule design (Matjuschkin et al, 2015) to control oxygen fugacity in piston cylinder experiments, along with high precision X-ray absorption techniques (XANES) to measure iron oxidation state in silicate glasses (Cottrell et al, 2009), we are able to constrain the H2O activity in silicate melts at under-saturated conditions. Preliminary results on an andesite melt with low H2O content (3 wt%) have been shown (Moore et al, 2016) to match predicted H2O activity values calculated using the H2O equation of state of Duan and Zhang (1996) and the H2O solubility model of Ghiorso and Gualda (2015). More recent results on the same andesite melt containing approximately 5 wt% H2O however show a large negative deviation from the predicted values. Reversal experiments involving an oxidized starting material are ongoing, as well as further characterization of the samples to detect the presence of possible contaminants that would induce reduction of the melt beyond that related to the H2O activity (e.g. graphite contamination).

Contrasting Impact of Future CO2 Emission Scenarios on the Extent of CaCO3 Mineral Undersaturation in the Humboldt Current System

Science.gov (United States)

Franco, A. C.; Gruber, N.; Frölicher, T. L.; Kropuenske Artman, L.

2018-03-01

The eastern boundary upwelling systems are among those regions that are most vulnerable to an ocean acidification-induced transition toward undersaturated conditions with respect to mineral CaCO3, but no assessment exists yet for the Humboldt Current System. Here we use a high-resolution (˜7.5 km) regional ocean model to investigate past and future changes in ocean pH and CaCO3 saturation state in this system. We find that within the next few decades, the nearshore waters off Peru are projected to become corrosive year round with regard to aragonite, the more soluble form of CaCO3. The volume of aragonite undersaturated water off Peru will continue to increase in the future irrespective of the amount of CO2 emitted to the atmosphere. In contrast, the development of the saturation state with regard to calcite, a less soluble form of carbonate, depends strongly on the scenario followed. By 2050, calcite undersaturation appears in the nearshore waters off Peru occasionally, but by 2090 in a high-emission scenario (RCP8.5), ˜60% of the water in the euphotic zone will become permanently calcite undersaturated. Most of this calcite undersaturation off Peru can likely be avoided if a low emission scenario (RCP2.6) consistent with the Paris Agreement is followed. The progression of ocean acidification off Chile follows a similar pattern, except that the saturation states are overall higher. But also here, calcite undersaturated waters will become common in the subsurface waters under the RCP8.5 scenario by the end of this century, while this can be avoided under the RCP2.6 scenario.

Evaluation of aqueous geochemistry of fluoride enriched groundwater: A case study of the Patan district, Gujarat, Western India

Directory of Open Access Journals (Sweden)

Pankaj Kumar

2017-10-01

Saturation index for selected minerals suggests that most of the samples are oversaturated with calcite and undersaturated with fluorite. Calcite precipitation leads to the removal of Ca2+ from solution thus allowing more fluorite to dissolve. These released Ca2+ ions combine with CO32− ions to further enhance the precipitation of CaCO3.

Maps showing predicted probabilities for selected dissolved oxygen and dissolved manganese threshold events in depth zones used by the domestic and public drinking water supply wells, Central Valley, California

Science.gov (United States)

Rosecrans, Celia Z.; Nolan, Bernard T.; Gronberg, JoAnn M.

2018-01-31

The purpose of the prediction grids for selected redox constituents—dissolved oxygen and dissolved manganese—are intended to provide an understanding of groundwater-quality conditions at the domestic and public-supply drinking water depths. The chemical quality of groundwater and the fate of many contaminants is influenced by redox processes in all aquifers, and understanding the redox conditions horizontally and vertically is critical in evaluating groundwater quality. The redox condition of groundwater—whether oxic (oxygen present) or anoxic (oxygen absent)—strongly influences the oxidation state of a chemical in groundwater. The anoxic dissolved oxygen thresholds of water, making drinking water undesirable with respect to taste, staining, or scaling. Three dissolved manganese thresholds, supply water wells. The 50 µg/L event threshold represents the secondary maximum contaminant level (SMCL) benchmark for manganese (U.S. Environmental Protection Agency, 2017; California Division of Drinking Water, 2014), whereas the 300 µg/L event threshold represents the U.S. Geological Survey (USGS) health-based screening level (HBSL) benchmark, used to put measured concentrations of drinking-water contaminants into a human-health context (Toccalino and others, 2014). The 150 µg/L event threshold represents one-half the USGS HBSL. The resultant dissolved oxygen and dissolved manganese prediction grids may be of interest to water-resource managers, water-quality researchers, and groundwater modelers concerned with the occurrence of natural and anthropogenic contaminants related to anoxic conditions. Prediction grids for selected redox constituents and thresholds were created by the USGS National Water-Quality Assessment (NAWQA) modeling and mapping team.

Origin and Evolution of Reactive and Noble Gases Dissolved in Matrix Pore Water

Energy Technology Data Exchange (ETDEWEB)

Eichinger, F. [Hydroisotop GmbH, Schweitenkirchen (Germany); Rock-Water Interaction, Institute of Geological Sciences, University of Bern, Bern (Switzerland); Waber, H. N. [Rock-Water Interaction, Institute of Geological Sciences, University of Bern, Bern (Switzerland); Smellie, J. A.T. [Conterra AB, Stockholm (Sweden)

2013-07-15

Reactive and noble gases dissolved in matrix pore water of low permeable crystalline bedrock were successfully extracted and characterized for the first time based on drillcore samples from the Olkiluoto investigation site (SW Finland). Interaction between matrix pore water and fracture groundwater occurs predominately by diffusion. Changes in the chemical and isotopic composition of gases dissolved in fracture groundwater are transmitted and preserved in the pore water. Absolute concentrations, their ratios and the stable carbon isotope signature of hydrocarbon gases dissolved in pore water give valuable indications about the evolution of these gases in the nearby flowing fracture groundwaters. Inert noble gases dissolved in matrix pore water and their isotopes combined with their in situ production and accumulation rates deliver information about the residence time of pore water. (author)

Study of Factors Influencing Oxygen-18 Isotopic Contents of Dissolved Sulphate in the Shallow Groundwater In Karawang Area

International Nuclear Information System (INIS)

Ristin Pujiindiyati, E.; Bungkus Pratikno

2010-01-01

The study was conducted to investigate the factors influencing oxygen-18 isotopic contents of dissolved sulphate in shallow groundwater from Karawang area. The δ 18 O is a relative abundance of O-18 compared to O-16 in CO 2 gas. CO 2 gas was released from the equilibrium between water samples and CO 2 gas, and from the reduction of sulphate samples with graphite. From this investigation, the δ 18 O (H 2 O) values were in the range of -3.21 0 / 00 to 6.25 0 / 00 whereas the δ 18 O (SO 4 2- ) values were 9.64 0 / 00 to 20.72 0 / 00 . The wide variation of δ 18 O (SO 4 2- ) values might be result due to inhomogeneity of sulphate sources in groundwater where the groundwater sulphates were generally derived from the dissolution of marine evaporites rocks. The groundwaters and Citarum River near waters to Johar site showed lowering of δ 18 O (SO 4 2- ) values. It might be related to the present of the traditional market in this location. The lowering of these values might be due to the increase of the sulphate reduction process caused by anaerobic bacteria growth in organic garbage deposition. Plotting between δ 18 O (SO 4 2- ) and δ 18 O (H 2 O) exhibited that the oxygen contribution from H 2 O to form sulphate was less than 25%. This indicated that the shallow groundwater in Karawang is located in a non-saturated zone and had a biotic condition. (author)

Molecular characterisation of dissolved organic matter (DOM) in groundwaters from the Aespoe Underground Research Laboratory (Sweden)): A novel 'finger printing' tool for palaeo-hydrological assessment

International Nuclear Information System (INIS)

Vane, C. H.; Kim, A. W.; Milodowski, A. E.; Smellie, J.; Tullborg, E. L.; West, J. M.

2008-01-01

The molecular signature of dissolved organic matter (DOM) in groundwaters can be used as a tool when investigating the palaeo-hydrological response of groundwater systems in relation to changes in recharge environment, and also for examining groundwater compartmentalisation, mixing and transport at underground repositories for radioactive waste. The DOM in groundwaters from two compartmentalised bodies of groundwater of distinctly different origin within the Aespoe Underground Research Laboratory (URL) (Sweden)) and in Baltic seawater has been isolated using tangential flow ultrafiltration (TUF) and dia-filtration. Recoveries of DOM ranged from 34.7 to 0.1 mg/L with substantial differences in the concentrations of the groundwaters collected only 120 m apart. Analysis by infrared spectroscopy (IR) and pyrolysis gas chromatography-mass spectrometry (Py-GC-MS) of the isolated DOM revealed that the groundwaters contained abundant alkylphenols which may represent heavily decomposed proteins or lignins originating from biopolymers contained within soils. The difference in the distribution and relative abundance of major pyrolysis products groups such as alkylphenols confirmed that the groundwater and Baltic seawater DOM samples were chemically distinct indicating minimal infiltration of marine groundwater derived by recharge from the Baltic or earlier Littorina Sea within the two compartmentalised groundwater bodies. (authors)

Groundwater and solute transport modeling at Hyporheic zone of upper part Citarum River

Science.gov (United States)

Iskandar, Irwan; Farazi, Hendy; Fadhilah, Rahmat; Purnandi, Cipto; Notosiswoyo, Sudarto

2017-06-01

Groundwater and surface water interaction is an interesting topic to be studied related to the water resources and environmental studies. The study of interaction between groundwater and river water at the Upper Part Citarum River aims to know the contribution of groundwater to the river or reversely and also solute transport of dissolved ions between them. Analysis of drill logs, vertical electrical sounding at the selected sections, measurement of dissolved ions, and groundwater modeling were applied to determine the flow and solute transport phenomena at the hyporheic zone. It showed the hyporheic zone dominated by silt and clay with hydraulic conductivity range from 10-4∼10-8 m/s. The groundwater flowing into the river with very low gradient and it shows that the Citarum River is a gaining stream. The groundwater modeling shows direct seepage of groundwater into the Citarum River is only 186 l/s, very small compared to the total discharge of the river. Total dissolved ions of the groundwater ranged from 200 to 480 ppm while the river water range from 200 to 2,000 ppm. Based on solute transport modeling it indicates dissolved ions dispersion of the Citarum River into groundwater may occur in some areas such as Bojongsoang-Dayeuh Kolot and Nanjung. This situation would increase the dissolved ions in groundwater in the region due to the contribution of the Citarum River. The results of the research can be a reference for further studies related to the mechanism of transport of the pollutants in the groundwater around the Citarum River.

Radiation induced homogeneous precipitation in undersaturated solid-solutions

International Nuclear Information System (INIS)

Cauvin, Richard; Martin, Georges.

1978-01-01

The stability of various types of solid solutions under irradiation is studied. In this paper, observations made on AlZn solid solutions under 1 MeV electron irradiation are reported. Al-Zn was chosen as a prototype of solid solutions with a simple miscibility gap. It is shown that under appropriate irradiation conditions undersaturated AnZn solid solutions give rise to a homogeneous precipitation of coherent G.P. zones and of incoherent Zn precipitates the atomic volume of which is smaller than that of the matrix. We propose a more general treatment of solute concentration heterogeneities in solid solutions under irradiation and suggest how it might account for the nucleation of the observed phases. The growth of the observed precipitates is studied

Determination of the origin of dissolved inorganic carbon in groundwater around a reclaimed landfill in Otwock using stable carbon isotopes.

Science.gov (United States)

Porowska, Dorota

2015-05-01

Chemical and isotopic analyses of groundwater from piezometers located around a reclaimed landfill in Otwock (Poland) were performed in order to trace the origin of dissolved inorganic carbon (DIC) in the groundwater. Due to differences in the isotopic composition of carbon from different sources, an analysis of stable carbon isotopes in the groundwater, together with the Keeling plot approach and a two-component mixing model allow us to evaluate the relative contributions of carbon from these sources in the groundwater. In the natural (background) groundwater, DIC concentrations and the isotopic composition of DIC (δ(13)CDIC) comes from two sources: decomposition of organic matter and carbonate dissolution within the aquifer sediments, whereas in the leachate-contaminated groundwater, DIC concentrations and δ(13)CDIC values depend on the degradation of organic matter within the aquifer sediments and biodegradation of organic matter stored in the landfill. From the mixing model, about 4-54% of the DIC pool is derived from organic matter degradation and 96-46% from carbonate dissolution in natural conditions. In the leachate-contaminated groundwater, about 20-53% of the DIC is derived from organic matter degradation of natural origin and 80-47% from biodegradation of organic matter stored in the landfill. Partial pressure of CO2 (P CO2) was generally above the atmospheric, hence atmospheric CO2 as a source of carbon in DIC pool was negligible in the aquifer. P CO2 values in the aquifer in Otwock were always one to two orders of magnitude above the atmospheric P CO2, and thus CO2 escaped directly into the vadose zone. Copyright © 2015 Elsevier Ltd. All rights reserved.

Association between arsenic and different-sized dissolved organic matter in the groundwater of black-foot disease area, Taiwan.

Science.gov (United States)

Chen, Ting-Chien; Hseu, Zeng-Yei; Jean, Jiin-Shuh; Chou, Mon-Lin

2016-09-01

The formation of an arsenic (As)-dissolved organic matter (DOM) complex is important in driving the release of arsenic in groundwater. This study collected groundwater samples from a 20 m deep well throughout 2014 and separated each into three subsamples by ultrafiltration: high molecular weight-DOM (HDOM, 0.45 μm-10 kDa), medium molecular weight-DOM (MDOM, 10-1 kDa), and low molecular weight-DOM (LDOM, arsenic and the fractional DOM. Based on the EEM records, three fluorescence indicators were further calculated to characterize the DOM sources, including the fluorescence index (FI), the biological index (BI), and the humification index (HI). The experimental results indicated that arsenic in the groundwater was mainly partitioned into the MDOM and LDOM fractions. All fractional DOMs contained humic acid-like substances and were considered as microbial sources. LDOM had the highest humification degree and aromaticity, followed by MDOM and HDOM. The As and DOM association could be formed by a Fe-bridge, which was demonstrated by the Ks values and fourier transform infrared (FTIR) spectra of the DOM. The formation of AsFe-DOM complex was only significant in the MDOM and LDOM. Copyright © 2016 Elsevier Ltd. All rights reserved.

Shifting nitrous oxide source/sink behaviour in a subtropical estuary revealed by automated time series observations

Science.gov (United States)

Reading, Michael J.; Santos, Isaac R.; Maher, Damien T.; Jeffrey, Luke C.; Tait, Douglas R.

2017-07-01

The oceans are a major source of the potent greenhouse gas nitrous oxide (N2O) to the atmosphere. However, little information is available on how estuaries and the coastal ocean may contribute to N2O budgets, and on the drivers of N2O in aquatic environments. This study utilised five time series stations along the freshwater to marine continuum in a sub-tropical estuary in Australia (Coffs Creek, Australia). Each time series station captured N2O, radon (222Rn, a natural submarine groundwater discharge tracer), dissolved nitrogen, and dissolved organic carbon (DOC) concentrations for a minimum of 25 h. The use of automated time series observations enabled spatial and tidal-scale variability of N2O to be captured. Groundwater was highly enriched in N2O (up to 306 nM) compared to the receiving surface water. Dissolved N2O supersaturation as high as 386% (27.4 nM) was observed in the upstream freshwater and brackish water areas which represented only a small (∼13%) proportion of the total estuary area. A large area of N2O undersaturation (as low as 53% or 3.9 nM) was observed in the mangrove-dominated lower estuary. This undersaturated area likely resulted from N2O consumption due to nitrate/nitrite (NOx) limitation in mangrove sediments subject to shallow porewater exchange. Overall, the estuary was a minor source of N2O to the atmosphere as the lower mangrove-dominated estuary sink of N2O counteracted groundwater-dominated source of N2O in the upper estuary. Average area-weighted N2O fluxes at the water-air interface approached zero (0.2-0.7 μmol m-2 d-1, depending on piston velocity model used), and were much lower than nitrogen-rich Northern Hemisphere estuaries that are considered large sources of N2O to the atmosphere. This study revealed a temporally and spatially diverse estuary, with areas of N2O production and consumption related to oxygen and total dissolved nitrogen availability, submarine groundwater discharge, and uptake within mangroves.

Yucca Mountain Area Saturated Zone Dissolved Organic Carbon Isotopic Data

International Nuclear Information System (INIS)

Thomas, James; Decker, David; Patterson, Gary; Peterman, Zell; Mihevc, Todd; Larsen, Jessica; Hershey, Ronald

2007-01-01

Groundwater samples in the Yucca Mountain area were collected for chemical and isotopic analyses and measurements of water temperature, pH, specific conductivity, and alkalinity were obtained at the well or spring at the time of sampling. For this project, groundwater samples were analyzed for major-ion chemistry, deuterium, oxygen-18, and carbon isotopes of dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC). The U.S. Geological Survey (USGS) performed all the fieldwork on this project including measurement of water chemistry field parameters and sample collection. The major ions dissolved in the groundwater, deuterium, oxygen-18, and carbon isotopes of dissolved inorganic carbon (DIC) were analyzed by the USGS. All preparation and processing of samples for DOC carbon isotopic analyses and geochemical modeling were performed by the Desert Research Institute (DRI). Analysis of the DOC carbon dioxide gas produced at DRI to obtain carbon-13 and carbon-14 values was conducted at the University of Arizona Accelerator Facility (a NSHE Yucca Mountain project QA qualified contract facility). The major-ion chemistry, deuterium, oxygen-18, and carbon isotopes of DIC were used in geochemical modeling (NETPATH) to determine groundwater sources, f ow paths, mixing, and ages. The carbon isotopes of DOC were used to calculate groundwater ages that are independent of DIC model corrected carbon-14 ages. The DIC model corrected carbon-14 calculated ages were used to evaluate groundwater travel times for mixtures of water including water beneath Yucca Mountain. When possible, groundwater travel times were calculated for groundwater flow from beneath Yucca Mountain to down gradient sample sites. DOC carbon-14 groundwater ages were also calculated for groundwaters in the Yucca Mountain area. When possible, groundwater travel times were estimated for groundwater flow from beneath Yucca Mountain to down gradient groundwater sample sites using the DOC calculated

Isotope-geochemical studies on fractions of dissolved organic carbon (DOC) for determining the origin and evolution of DOC for purposes of groundwater dating

International Nuclear Information System (INIS)

Geyer, S.

1994-01-01

The laboratory work consisted in developing and testing methods of extraction and enrichment of individual high-purity DOC fractions (fulvic acids, humic acids, and low-molecular substances) with the aim of preparing large quantities of groundwaters (> 1000 l) with low DOC concentrations so as to obtain sufficient sampling material. Chemical characterisation of DOC consisted in an analysis of humic and fulvic acids with regard to element composition (C, H, N, O, S) and inorganic trace elements. Isotopic characterization of the DOC fractions consisted in determining 14 C, 13 C, and 2 H levels. For the first time δ 34 S and δ 15 N relations in humic and fulvic acids dissolved in groundwater were determined. (orig./DG) [de

Determination of the origin of dissolved inorganic carbon in groundwater around a reclaimed landfill in Otwock using stable carbon isotopes

Energy Technology Data Exchange (ETDEWEB)

Porowska, Dorota, E-mail: dorotap@uw.edu.pl

2015-05-15

Highlights: • Research showed the origin of DIC in the groundwater around a reclaimed landfill. • Carbon isotope was used to evaluate the contributions of carbon from different sources. • The leachate-contaminated water was isotopically distinct from the natural groundwater. • DIC in the natural groundwater comes from organic matter and dissolution of carbonates. • In the contaminated water, DIC comes from organic matter in the aquifer and landfill. - Abstract: Chemical and isotopic analyses of groundwater from piezometers located around a reclaimed landfill in Otwock (Poland) were performed in order to trace the origin of dissolved inorganic carbon (DIC) in the groundwater. Due to differences in the isotopic composition of carbon from different sources, an analysis of stable carbon isotopes in the groundwater, together with the Keeling plot approach and a two-component mixing model allow us to evaluate the relative contributions of carbon from these sources in the groundwater. In the natural (background) groundwater, DIC concentrations and the isotopic composition of DIC (δ{sup 13}C{sub DIC}) comes from two sources: decomposition of organic matter and carbonate dissolution within the aquifer sediments, whereas in the leachate-contaminated groundwater, DIC concentrations and δ{sup 13}C{sub DIC} values depend on the degradation of organic matter within the aquifer sediments and biodegradation of organic matter stored in the landfill. From the mixing model, about 4–54% of the DIC pool is derived from organic matter degradation and 96–46% from carbonate dissolution in natural conditions. In the leachate-contaminated groundwater, about 20–53% of the DIC is derived from organic matter degradation of natural origin and 80–47% from biodegradation of organic matter stored in the landfill. Partial pressure of CO{sub 2} (P CO{sub 2}) was generally above the atmospheric, hence atmospheric CO{sub 2} as a source of carbon in DIC pool was negligible in the

Air sparging of organic compounds in groundwater

International Nuclear Information System (INIS)

Hicks, P.M.

1994-01-01

Soils and aquifers containing organic compounds have been traditionally treated by excavation and disposal of the soil and/or pumping and treating the groundwater. These remedial options are often not practical or cost effective solutions. A more favorable alternative for removal of the adsorbed/dissolved organic compounds would be an in situ technology. Air sparging will remove volatile organic compounds from both the adsorbed and dissolved phases in the saturated zone. This technology effectively creates a crude air stripper below the aquifer where the soil acts as the ''packing''. The air stream that contacts dissolved/adsorbed phase organics in the aquifer induces volatilization. A case history illustrates the effectiveness of air sparging as a remedial technology for addressing organic compounds in soil and groundwater. The site is an operating heavy equipment manufacturing facility in central Florida. The soil and groundwater below a large building at the facility was found to contain primarily diesel type petroleum hydrocarbons during removal of underground storage tanks. The organic compounds identified in the groundwater were Benzene, Xylenes, Ethylbenzene and Toluenes (BTEX), Methyl tert-Butyl Ether (MTBE) and naphthalenes in concentrations related to diesel fuel

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.

Brackish groundwater in the United States

Science.gov (United States)

Stanton, Jennifer S.; Anning, David W.; Brown, Craig J.; Moore, Richard B.; McGuire, Virginia L.; Qi, Sharon L.; Harris, Alta C.; Dennehy, Kevin F.; McMahon, Peter B.; Degnan, James R.; Böhlke, John Karl

2017-04-05

in the United States. Previously published digital data relating to brackish groundwater resources were limited to a small number of State- and regional-level studies. Data sources for this assessment ranged from single publications to large datasets and from local studies to national assessments. Geochemical data included concentrations of dissolved solids, major ions, trace elements, nutrients, and radionuclides as well as physical properties of the water (pH, temperature, and specific conductance). Additionally, the database provides selected well information (location, yield, depth, and contributing aquifer) necessary for evaluating the water resource.The assessment was divided into national-, regional-, and aquifer-scale analyses. National-scale analyses included evaluation of the three-dimensional distribution of observed dissolved-solids concentrations in groundwater, the three-dimensional probability of brackish groundwater occurrence, and the geochemical characteristics of saline (greater than or equal to 1,000 mg/L of dissolved solids) groundwater resources. Regional-scale analyses included a summary of the percentage of observed grid cell volume in the region that was occupied by brackish groundwater within the mixture of air, water, and rock for multiple depth intervals. Aquifer-scale analyses focused primarily on four regions that contained the largest amounts of observed brackish groundwater and included a generalized description of hydrogeologic characteristics from previously published work; the distribution of dissolved-solids concentrations; considerations for developing brackish groundwater resources, including a summary of other chemical characteristics that may limit the use of brackish groundwater and the ability of sampled wells producing brackish groundwater to yield useful amounts of water; and the amount of saline groundwater being used in 2010.

Assessing the Impact of Animal Waste Lagoon Seepage on the Geochemistry of an Underlying Shallow Aquifer

Energy Technology Data Exchange (ETDEWEB)

McNab, W W; Singleton, M J; Moran, J E; Esser, B K

2006-03-07

Dairy facilities and similar confined animal operation settings pose a significant nitrate contamination threat via oxidation of animal wastes and subsequent transport to shallow groundwater. While nitrate contamination resulting from application of animal manure as fertilizer to fields is well recognized, the impact of manure lagoon leakage on groundwater quality is less well characterized. In this study, a dairy facility located in the southern San Joaquin Valley of California has been instrumented with monitoring wells as part of a two-year multidisciplinary study to evaluate nitrate loading and denitrification associated with facility operations. Among multiple types of data collected from the site, groundwater and surface water samples have been analyzed for major cations, anions, pH, oxidation-reduction potential, dissolved organic carbon, and selected dissolved gases (CO{sub 2}, CH{sub 4}, N{sub 2}, Ar, Ne). Modeling of putative geochemical processes occurring within the dairy site manure lagoons shows substantial off-gassing of CO{sub 2} and CH{sub 4} in response to mineralization of organic matter. The gas ebullition appears to strip dissolved gases, including Ar and Ne, from the lagoon water leaving concentrations that are undersaturated with respect to the atmosphere. The resulting fractionated dissolved gas signature serves as an effective tracer for the lagoon water in the underlying shallow groundwater and can be used to constrain inverse geochemical models that assess mixing fractions of lagoon water and local groundwater water. Together with ion exchange and mineral equilibria reactions, identification of lagoon seepage helps explain key attributes of the local groundwater chemistry, including input and cycling of nitrogen, across the site.

Investigating the salinization and freshening processes of coastal groundwater resources in Urmia aquifer, NW Iran.

Science.gov (United States)

Amiri, Vahab; Nakhaei, Mohammad; Lak, Razyeh; Kholghi, Majid

2016-04-01

This paper presents the results of an assessment about interaction between Urmia Lake (UL) and coastal groundwater in the Urmia aquifer (UA). This aquifer is the most significant contributor to the freshwater supply of the coastal areas. The use of hydrochemical facies can be very useful to identify the saltwater encroachment or freshening phases in the coastal aquifers. In this study, the analysis of salinization/freshening processes was carried out through the saturation index (SI), ionic deltas (Δ), binary diagrams, and hydrochemical facies evolution (HFE) diagram. Based on the Gibbs plot, the behavior of the major ions showed that the changes in the chemical composition of the groundwater are mainly controlled by the water-soil/rock interaction zone and few samples are relatively controlled by evaporation. A possible explanation for this phenomenon is that the deposited chloride and sulfate particles can form the minor salinity source in some coastal areas when washed down by precipitation. The SI calculations showed that all groundwater samples, collected in these periods, show negative saturation indices, which indicate undersaturation with respect to anhydrite, gypsum, and halite. In addition, except in a few cases, all other samples showed the undersaturation with respect to the carbonate minerals such as aragonite, calcite, and dolomite. Therefore, these minerals are susceptible to dissolution. In the dry season, the SI calculations showed more positive values with respect to dolomite, especially in the northern part of UA, which indicated a higher potential for precipitation and deposition of dolomite. The percentage of saltwater in the groundwater samples of Urmia plain was very low, ranging between 0.001 and 0.79 % in the wet season and 0.0004 and 0.81 % in the dry season. The results of HFE diagram, which was taken to find whether the aquifer was in the saltwater encroachment phase or in the freshening phase, indicated that except for a few wells

Developing a Hygrometer for Water-Undersaturated Lherzolite Melts

Science.gov (United States)

Guild, M. R.; Till, C. B.

2017-12-01

The effect of water on the composition of primitive mantle melts at arc volcanoes is a topic of wide interest and has been addressed in a number of previous experimental studies including Hirose & Kawamoto (1995), Gaetani & Grove (1998), Till et al. (2012) and Mitchell & Grove (2015). The current study builds upon the work by previous authors in an effort to develop a more robust hygrometer for primitive lherzolite melts at water-undersaturated conditions. The starting composition for this experimental study is a mixture of 75% primitive upper mantle and 25% primitive basalt (Baker et al., 1991) with a bulk H2O content of 2 wt. %. Experiments were performed at Arizona State University in the Experimental Petrology and Igneous processes Center (EPIC) from 1.2-1.6 GPa at 1150-1300 ºC for 2 days in a piston cylinder apparatus to reflect conditions relevant for arc melt equilibration (Till 2017). A double capsule design was used to prevent Fe and H2O loss with an inner Fe-presaturated Au80Pd20 capsule and an outer Au80Pd20 capsule. Run products were analyzed by electron microprobe and determined to be successful when they demonstrated 0-5% Fe-loss, olivine-melt KDs of 0.27-0.30, and minimal H2O loss. The water-undersaturated melt composition are in equilibrium with ol+opx+sp±cpx. Run products at 1.6 GPa do not contain cpx in the mineral assemblage over the studied temperature range. Observed melt compositions have SiO2 contents of 48-49 wt. % at 1.2 GPa and 46-49 wt.% at 1.6 GPa. Our experimental results suggest an enhanced effect of water on increasing the SiO2 content of the melt compared to previous studies on systems with similar water contents and anhydrous systems. Baker, et al., JGR 96, 21819-21842 (1991). Gaetani & Grove, CMP 131, 323-346 (1998). Hirose & Kawamoto, EPSL 133, 463-473 (1995). Mitchell & Grove, CMP 170, 13 (2015). Till, Am. Mineral, 102, 931-947 (2017). Till, et al., JGR 117 (2012).

The role of baseflow in dissolved solids delivery to streams in the Upper Colorado River Basin

Science.gov (United States)

Rumsey, C.; Miller, M. P.; Schwarz, G. E.; Susong, D.

2017-12-01

Salinity has a major effect on water users in the Colorado River Basin, estimated to cause almost $300 million per year in economic damages. The Colorado River Basin Salinity Control Program implements and manages projects to reduce salinity (dissolved solids) loads, investing millions of dollars per year in irrigation upgrades, canal projects, and other mitigation strategies. To inform and improve mitigation efforts, there is a need to better understand sources of salinity to streams and how salinity has changed over time. This study explores salinity in baseflow, or groundwater discharge to streams, to assess whether groundwater is a significant contributor of dissolved solids to streams in the Upper Colorado River Basin (UCRB). Chemical hydrograph separation was used to estimate long-term mean annual baseflow discharge and baseflow dissolved solids loads at stream gages (n=69) across the UCRB. On average, it is estimated that 89% of dissolved solids loads originate from the baseflow fraction of streamflow. Additionally, a statistical trend analysis using weighted regressions on time, discharge, and season was used to evaluate changes in baseflow dissolved solids loads in streams with data from 1987 to 2011 (n=29). About two-thirds (62%) of these streams showed statistically significant decreasing trends in baseflow dissolved solids loads. At the two most downstream sites, Green River at Green River, UT and Colorado River at Cisco, UT, baseflow dissolved solids loads decreased by a combined 780,000 metric tons, which is approximately 65% of the estimated basin-scale decrease in total dissolved solids loads in the UCRB attributed to salinity control efforts. Results indicate that groundwater discharged to streams, and therefore subsurface transport processes, play a large role in delivering dissolved solids to streams in the UCRB. Decreasing trends in baseflow dissolved solids loads suggest that salinity mitigation projects, changes in land use, and/or climate are

Modeling Dissolved Solids in the Rincon Valley, New Mexico Using RiverWare

Science.gov (United States)

Abudu, S.; Ahn, S. R.; Sheng, Z.

2017-12-01

Simulating transport and storage of dissolved solids in surface water and underlying alluvial aquifer is essential to evaluate the impacts of surface water operations, groundwater pumping, and climate variability on the spatial and temporal variability of salinity in the Rio Grande Basin. In this study, we developed a monthly RiverWare water quantity and quality model to simulate the both concentration and loads of dissolved solids for the Rincon Valley, New Mexico from Caballo Reservoir to Leasburg Dam segment of the Rio Grande. The measured flows, concentration and loads of dissolved solids in the main stream and drains were used to develop RiveWare model using 1980-1988 data for calibration, and 1989-1995 data for validation. The transport of salt is tracked using discretized salt and post-process approaches. Flow and salt exchange between the surface water and adjacent groundwater objects is computed using "soil moisture salt with supplemental flow" method in the RiverWare. In the groundwater objects, the "layered salt" method is used to simulate concentration of the dissolved solids in the shallow groundwater storage. In addition, the estimated local inflows under different weather conditions by using a calibrated Soil Water Assessment Tool (SWAT) were fed into the RiverWare to refine the simulation of the flow and dissolved solids. The results show the salt concentration and loads increased at Leasburg Dam, which indicates the river collects salts from the agricultural return flow and the underlying aquifer. The RiverWare model with the local inflow fed by SWAT delivered the better quantification of temporal and spatial salt exchange patterns between the river and the underlying aquifer. The results from the proposed modeling approach can be used to refine the current mass-balance budgets for dissolved-solids transport in the Rio Grande, and provide guidelines for planning and decision-making to control salinity in arid river environment.

34S and 18O in dissolved sulfate as tracers of hydrogeochemical evolution of the Triassic carbonate aquifer exposed to intense groundwater exploitation (Olkusz-Zawiercie region, southern Poland)

International Nuclear Information System (INIS)

Samborska, Katarzyna; Halas, Stanislaw

2010-01-01

Research highlights: → Groundwater table rebound in aquifer containing sulfide ore. → Degradation of water quality causes by the significant increase in sulfate concentrations. → Isotopic examinations of sulfate and sulfate concentrations along flow path. → Sulfate concentrations as a result of binary mixing of sources (sulfide and evaporate). → Changes in isotopic composition of sulfide in extended vadose zone. - Abstract: The objective of this study was to determine the sources of SO 4 2- in groundwater of the Olkusz-Zawiercie Major Groundwater Body. The quality of groundwater was relatively good in the past, but fluctuations of the water table level have caused degradation of water quality. Variations in the water table level and the formation of the depression cone have resulted from both groundwater withdrawal and Zn-Pb mine dewatering. As a result within the extended vadose zone of the aquifer, weathering of pyrite and accompanying sulfides has taken place. Since 1992 the water table has risen and this process has been associated with an increase in concentrations of SO 4 2- , Ca and Mg. At the same time, the pH has decreased and periodically high Fe concentrations have been detected. High concentrations of Mg and Sr have been observed and, since gypsum layers are known to be present, a de-dolomitisation process has been hypothesized. The PHREEQC program for Windows was used to estimate saturation indices for calcite, dolomite, gypsum and epsomite. Isotopic data for SO 4 2- dissolved in the groundwater and archival data on isotopic composition of ore sulfides were used to solve the isotope balance equation and to estimate the fraction of dissolved SO 4 2- that originated from pyrite oxidation and gypsum dissolution. The results have shown that dissolution of pyrite oxidation products has a significant influence on chemical composition of groundwater, especially in the southern part of the cone of depression. By solving the additional, combined mass

Redox control of arsenic mobilization in Bangladesh groundwater

International Nuclear Information System (INIS)

Zheng, Y.; Stute, M.; Geen, A. van; Gavrieli, I.; Dhar, R.; Simpson, H.J.; Schlosser, P.; Ahmed, K.M.

2004-01-01

Detailed hydrochemical measurements, δ 34 S SO4 and 3 H analyses were performed on 37 groundwater samples collected during February 1999, January and March 2000 from 6 locations in eastern and southeastern Bangladesh to examine redox processes that lead to As mobilization in groundwater. The study sites were chosen based on available nation-wide As surveys to span the entire spectrum of As concentrations in Bangladesh groundwater, and to represent 3 of 5 major geological units of the Ganges-Brahmaputra Delta: uplifted Pleistocene terrace, fluvial flood plain and delta plain. Arsenic was found to be mobilized under Fe-reducing conditions in shallow aquifers ( 4 -reducing conditions, suggesting that authigenic sulfide precipitation does not constitute a significant sink for As in these groundwaters. The redox state of the water was characterized by a variety of parameters including dissolved O 2 , NO 3 - , Mn 2+ , Fe 2+ concentrations, and SO 4 2- /Cl - ratios. High dissolved [As] (> 50 μg/l; or > 0.7 μM ) were always accompanied by high dissolved [HCO 3 - ] (> 4 mM), and were close to saturation with respect to calcite. Groundwater enriched in As (200-800 μg/l; or 2.7-10.7 μM) and phosphate (30-100 μM) but relatively low in dissolved Fe (5-40 μM) probably resulted from re-oxidation of reducing, As and Fe enriched water. This history was deduced from isotopic signatures of δ 34 S SO4 and 3 H 2 O ( 3 H) to delineate the nature of redox changes for some of the reducing groundwaters. In contrast, As is not mobilized in presumed Pleistocene aquifers, both shallow (30-60 m) and deep (150-270 m), because conditions were not reducing enough due to lack of sufficient O 2 demand

Iron oxidation kinetics and phosphorus immobilization at the groundwater-surface water interface

Science.gov (United States)

van der Grift, Bas; Rozemeijer, Joachim; Griffioen, Jasper; van der Velde, Ype

2014-05-01

Eutrophication of freshwater environments following diffuse nutrient loads is a widely recognized water quality problem in catchments. Fluxes of non-point P sources to surface waters originate from surface runoff and flow from soil water and groundwater into surface water. The availability of P in surface waters is controlled strongly by biogeochemical nutrient cycling processes at the soil-water interface. The mechanisms and rates of the iron oxidation process with associated binding of phosphate during exfiltration of anaerobic Fe(II) bearing groundwater are among the key unknowns in P retention processes in surface waters in delta areas where the shallow groundwater is typically pH-neutral to slightly acid, anoxic, iron-rich. We developed an experimental field set-up to study the dynamics in Fe(II) oxidation and mechanisms of P immobilization at the groundwater-surface water interface in an agricultural experimental catchment of a small lowland river. We physically separated tube drain effluent from groundwater discharge before it entered a ditch in an agricultural field. The exfiltrating groundwater was captured in in-stream reservoirs constructed in the ditch. Through continuous discharge measurements and weekly water quality sampling of groundwater, tube drain water, exfiltrated groundwater, and ditch water, we quantified Fe(II) oxidation kinetics and P immobilization processes across the seasons. This study showed that seasonal changes in climatic conditions affect the Fe(II) oxidation process. In winter time the dissolved iron concentrations in the in-stream reservoirs reached the levels of the anaerobic groundwater. In summer time, the dissolved iron concentrations of the water in the reservoirs are low, indicating that dissolved Fe(II) is completely oxidized prior to inflow into the reservoirs. Higher discharges, lower temperatures and lower pH of the exfiltrated groundwater in winter compared to summer shifts the location of the redox transition zone

Groundwater Quality Assessment Based on Geographical Information System and Groundwater Quality Index

Directory of Open Access Journals (Sweden)

Zahra Derakhshan

2015-06-01

Full Text Available Iran is located in an arid and semi-arid part of the world. Accordingly, the management of the water resources in the country is a priority. In this regard, determining the quality and pollution of surface water and groundwater is very important, especially in areas where groundwater resources are used for drinking. Groundwater quality index (GQI checks the components of the available water with various quality levels. To assess the quality of drinking groundwater of Yazd-Ardakan plain according to GQI in geographical information system (GIS environment, the electrical conductivity, sodium, calcium, magnesium, chlorine, pH, sodium adsorption ratio, bicarbonate, sulfate, potassium, water hardness, and all substances dissolved in the waters of 80 wells were determined. The samples were obtained from Yazd Regional Water Organization from 2005 to 2014. Using this data, the map components were plotted by Kriging geostatistical method. Then, the map of GQI was prepared after normalizing each map component, switching to a rating map, and extracting the weight of each component from the rating map. Based on the GQI index map, the index point which was 87 in 2005 has increased to 81 in 2014. These maps show a decline in groundwater quality from west to the east region. This decline in groundwater quality is due to the existence of Neogene Organizations in the east and geomorphologic unit of the bare epandage pediment in the west. The map removal and single-parameter sensitivity analysis showed that GQI index in Yazd-Ardakan plain is more sensitive to the components of electrical conductivity (EC, total dissolved solids (TDS, and total hardness (TH. Therefore, these components should be monitored more carefully and repeatedly.

Using dissolved gases to observe the evolution of groundwater age in a mountain watershed over a period of thirteen years

Science.gov (United States)

Manning, Andrew H.

2011-01-01

Baseflows in snowmelt-dominated mountain streams are critical for sustaining ecosystems and water resources during periods of greatest demand. Future climate predictions for mountainous areas throughout much of the western U.S. include increasing temperatures, declining snowpacks, and earlier snowmelt periods. The degree to and rate at which these changes will affect baseflows in mountain streams remains unknown, largely because baseflows are groundwater-fed and the relationship between climate and groundwater recharge/discharge rates in mountain watersheds is uncertain. We use groundwater age determinations from multiple dissolved gas tracers (CFCs, SF6, and 3H/3He) to track changes in groundwater age over a period of thirteen years in the Sagehen Creek watershed, Sierra Nevada Mountains, CA. Data were collected from springs and wells in 2009 and 2010 and combined with those obtained in prior studies from 1997 to 2003. Apparent ages range from 0 to >60 years. Comparison between variations in age and variations in snow water equivalent (SWE) and mean annual air temperature reveals the degree of correlation between these climate variables and recharge rate. Further, comparison of apparent ages from individual springs obtained at different times and using different tracers helps constrain the age distribution in the sampled waters. The age data are generally more consistent with an exponential age distribution than with piston-flow. However, many samples, even those with relatively old mean ages, must have a disproportionately large very young fraction that responds directly to annual SWE variations. These findings have important implications for how future baseflows may respond to decreasing SWE.

Metabolic Energy Demand Is Not Increased during Initial Shell Formation of Bivalves Exposed to Aragonite Undersaturation

Science.gov (United States)

Pan, F.; Frieder, C.; Applebaum, S.; Manahan, D. T.

2016-02-01

The Pacific oyster, Crassostrea gigas, is a major commercial species in global aquaculture. Ocean acidification is having a negative effect on larval production of this species, so the mechanisms of this impact are of considerable interest. Formation of new shell in C. gigas during the first 2-days post-fertilization results in a rapid six-fold increase in total mass. This period of early development has high sensitivity to changes in carbonate chemistry, in particular aragonite saturation state (Ω). An elevated energy cost for calcification at low Ω is often invoked as a mechanism. In this study, we characterized the developmental progression of first shell formation, total metabolic expenditure, and underlying biochemical processes of energy allocation during early development of C. gigas, under control (Ω >> 1) and undersaturated conditions (Ω pump activity (Na+, K+-ATPase) between the two treatments. We conclude that early development to the shelled-veliger larval stage does not require more energy at undersaturation. This finding helps constrain potential mechanisms of larval sensitivity to ocean acidification and narrows the focus for possible mitigation strategies for oyster aquaculture production.

Groundwater recharge and agricultural contamination

Science.gov (United States)

Böhlke, J.K.

2002-01-01

Agriculture has had direct and indirect effects on the rates and compositions of groundwater recharge and aquifer biogeochemistry. Direct effects include dissolution and transport of excess quantities of fertilizers and associated materials and hydrologic alterations related to irrigation and drainage. Some indirect effects include changes in water–rock reactions in soils and aquifers caused by increased concentrations of dissolved oxidants, protons, and major ions. Agricultural activities have directly or indirectly affected the concentrations of a large number of inorganic chemicals in groundwater, for example NO3–, N2, Cl, SO42–, H+, P, C, K, Mg, Ca, Sr, Ba, Ra, and As, as well as a wide variety of pesticides and other organic compounds. For reactive contaminants like NO3–, a combination of chemical, isotopic, and environmental-tracer analytical approaches might be required to resolve changing inputs from subsequent alterations as causes of concentration gradients in groundwater. Groundwater records derived from multi-component hydrostratigraphic data can be used to quantify recharge rates and residence times of water and dissolved contaminants, document past variations in recharging contaminant loads, and identify natural contaminant-remediation processes. These data indicate that many of the world's surficial aquifers contain transient records of changing agricultural contamination from the last half of the 20th century. The transient agricultural groundwater signal has important implications for long-term trends and spatial heterogeneity in discharge.

Nitrate in groundwater of the United States, 1991-2003

Science.gov (United States)

Burow, Karen R.; Nolan, Bernard T.; Rupert, Michael G.; Dubrovsky, Neil M.

2010-01-01

An assessment of nitrate concentrations in groundwater in the United States indicates that concentrations are highest in shallow, oxic groundwater beneath areas with high N inputs. During 1991-2003, 5101 wells were sampled in 51 study areas throughout the U.S. as part of the U.S. Geological Survey National Water-Quality Assessment (NAWQA) program. The well networks reflect the existing used resource represented by domestic wells in major aquifers (major aquifer studies), and recently recharged groundwater beneath dominant land-surface activities (land-use studies). Nitrate concentrations were highest in shallow groundwater beneath agricultural land use in areas with well-drained soils and oxic geochemical conditions. Nitrate concentrations were lowest in deep groundwater where groundwater is reduced, or where groundwater is older and hence concentrations reflect historically low N application rates. Classification and regression tree analysis was used to identify the relative importance of N inputs, biogeochemical processes, and physical aquifer properties in explaining nitrate concentrations in groundwater. Factors ranked by reduction in sum of squares indicate that dissolved iron concentrations explained most of the variation in groundwater nitrate concentration, followed by manganese, calcium, farm N fertilizer inputs, percent well-drained soils, and dissolved oxygen. Overall, nitrate concentrations in groundwater are most significantly affected by redox conditions, followed by nonpoint-source N inputs. Other water-quality indicators and physical variables had a secondary influence on nitrate concentrations.

Dissolved organic matter signatures vary between naturally acidic, circumneutral and groundwater-fed freshwaters in Australia.

Science.gov (United States)

Holland, Aleicia; Stauber, Jenny; Wood, Chris M; Trenfield, Melanie; Jolley, Dianne F

2018-06-15

Dissolved organic matter (DOM) plays important roles in both abiotic and biotic processes within aquatic ecosystems, and these in turn depend on the quality of the DOM. We collected and characterized chromophoric DOM (CDOM) from different Australian freshwater types (circumneutral, naturally acidic and groundwater-fed waterways), climatic regions and seasons. CDOM quality was characterized using absorbance and fluorescence spectroscopy. Excitation emission scans followed by parallel factor (PARAFAC) analysis showed that CDOM was characterized by three main components: protein-like, fulvic-like and humic-like components commonly associated with various waters globally in the Openfluor database. Principal component analysis showed that CDOM quality varied between naturally acidic, circumneutral and groundwater-fed waters, with unique CDOM quality signatures shown for each freshwater type. CDOM quality also differed significantly within some sites between seasons. Clear differences in dominant CDOM components were shown between freshwater types. Naturally acidic waters were dominated by highly aromatic (as indicated by the specific absorbance co-efficient (SAC 340 ) and the specific UV absorbance (SUVA 254 ) values which ranged between 31 and 50 cm 2  mg -1 and 3.9-5.7 mg C -1  m -1 respectively), humic-like CDOM of high molecular weight (as indicated by abs 254/365 which ranged from 3.8 to 4.3). In contrast, circumneutral waters were dominated by fulvic-like CDOM of lower aromaticity (SAC 340 : 7-21 cm 2  mg -1 and SUVA 254 : 1.5-3.0 mg C -1  m -1 ) and lower molecular weight (abs 254/365 5.1-9.3). The groundwater-fed site had a higher abundance of protein-like CDOM, which was the least aromatic (SAC 340 : 2-5 cm 2  mg -1 and SUVA 254 : 0.58-1.1 mg C -1  m -1 ). CDOM was generally less aromatic, of a lower molecular weight and more autochthonous in nature during the summer/autumn sampling compared to winter/spring. Significant

Hydrogeochemical and Isotopic Study of Groundwaters from the Gañuelas-Mazarrón Tertiary Basin (Murcia, Spain); Estudio Hidrogeoquímico e Isotópico de las Aguas de la Cuenca Terciaria de Gañuelas-Mazarrón (Murcia, España)

Energy Technology Data Exchange (ETDEWEB)

Rodrigo-Naharro, J.; Delgado, A.; Clemente-Jul, C.; Pérez del Villar, L.

2015-07-01

The hydrogeochemical characterisation of groundwaters from the Gañuelas-Mazarrón Tertiary Basin included: i) to establish the different hydrofacies present in the basin; ii) to perform a cluster analysis in order to reduce the water samples, grouping them according to their physicochemical characteristics; and iii) to determine the most relevant ion ratios for understanding the water/ rock interaction processes that regulate the main features and evolution of groundwaters. It has also been discussed the origin and concentration of the minor and trace elements to evaluate the capability of groundwaters to transport heavy elements, toxic or innocuous, towards the surface, thus determining their suitability for human consumption. Besides, the hydrogeochemical modeling has allowed determining the degree of groundwaters saturation with respect to the most representative mineral phases of the aquifers, which, in turn, it has been used to calculate their theoretical temperature in depth. The isotopic characterisation of groundwaters has included the isotopic signatures of the stable (δ18O, δ2H, δ13C-DIC, δ34S(SO4 2-) and δ18O(SO4 2-)) and radioactive (238U, 234U and 226Ra) isotopes. The first have been used to distinguish the groundwaters origin, as well as the origin of the dissolved C and SO4 2-. The radioactive isotopes have been used to determine the water/rock interaction processes involving 238U radioactive series, as well as to explain the origin of the dissolved 222Rn in groundwaters. The most important hydrogeochemical results obtained from groundwaters are: i) a large variety of hydrofacies is represented in them, corroborated by the cluster analysis; ii) they are not suitable for human consumption; iii) they have remained, apparently, over-saturated with respect to calcite and aragonite, and under-saturated with respect to gypsum, anhydrite and halite, over time; iv) they present theoretical temperatures in depth much higher than in the surface; v) they

Ground water dating on the basis of the 14C content of dissolved humic and fulvic acids. Final report

International Nuclear Information System (INIS)

Kim, J.I.; Artinger, R.; Buckau, G.; Kardinal, C.; Geyer, S.; Wolf, M.; Halder, H.; Fritz, P.

1995-05-01

The groundwater dating on the basis of the 14 C content of dissolved organic carbon (DOC) is studied. Fulvic acids (FA) and humic acids (HA) are used as DOC fractions. In addition, the groundwaters are dated with the 14 C content of the dissolved inorganic carbon (DIC). The isotopic contents of 2 H, 3 H, 13 C, 15 N, 18 O, and 34 S of groundwater and humic substances are alse determined. The isolated humic substances are characterized with regard to their chemical composition as well as their molecular size and spectroscopic properties. For aquifer systems which have a neglectable content of sedimentary organic carbon (SOC), the 14 C dating of FA show plausible groundwater ages. In aquifer systems with a high SOC content, the mixing of 14 C free FA from sediment partly falsifies the 14 C groundwater age as determined by dissolved FA. Due to the high transfer of HA from sediment to groundwater, HA are less suitable for groundwater dating. The FA characterization allows the distinction between FA of sedimentary origin and FA which infiltrate with seepage water. Several starting points for a correction of the calculated 14 C ages of FA exist. The results indicate, 14 C groundwater dating with fulvic acids is a valuable expansion of groundwater dating methods. (orig.) [de

Linking groundwater dissolved organic matter to sedimentary organic matter from a fluvio-lacustrine aquifer at Jianghan Plain, China by EEM-PARAFAC and hydrochemical analyses.

Science.gov (United States)

Huang, Shuang-bing; Wang, Yan-xin; Ma, Teng; Tong, Lei; Wang, Yan-yan; Liu, Chang-rong; Zhao, Long

2015-10-01

The sources of dissolved organic matter (DOM) in groundwater are important to groundwater chemistry and quality. This study examined similarities in the nature of DOM and investigated the link between groundwater DOM (GDOM) and sedimentary organic matter (SOM) from a lacustrine-alluvial aquifer at Jianghan Plain. Sediment, groundwater and surface water samples were employed for SOM extraction, optical and/or chemical characterization, and subsequent fluorescence excitation-emission matrix (EEM) and parallel factor analyses (PARAFAC). Spectroscopic properties of bulk DOM pools showed that indices indicative of GDOM (e.g., biological source properties, humification level, aromaticity and molecule mobility) varied within the ranges of those of two extracted end-members of SOM: humic-like materials and microbe-associated materials. The coexistence of PARAFAC compositions and the sustaining internal relationship between GDOM and extracted SOM indicate a similar source. The results from principal component analyses with selected spectroscopic indices showed that GDOM exhibited a transition trend regarding its nature: from refractory high-humification DOM to intermediate humification DOM and then to microbe-associated DOM, with decreasing molecular weight. Correlations of spectroscopic indices with physicochemical parameters of the groundwater suggested that GDOM was released from SOM and was modified by microbial diagenetic processes. The current study demonstrated the associations of GDOM with SOM from a spectroscopic viewpoint and provided new evidence supporting SOM as the source of GDOM. Copyright © 2015 Elsevier B.V. All rights reserved.

Dissolved nitrogen in drinking water resources of farming ...

African Journals Online (AJOL)

Dissolved nitrogen in drinking water resources of farming communities in Ghana. ... African Journal of Environmental Science and Technology ... Concentrations of these potentially toxic substances were below WHO acceptable limits for surface and groundwaters, indicating these water resources appear safe for drinking ...

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.

A groundwater mass flux model for screening the groundwater-to-indoor-air exposure pathway

Energy Technology Data Exchange (ETDEWEB)

McHugh, T.; Blanc, P.C. de; Connor, J. [Groundwater Services Inc, Houston, TX (United States)

2003-07-01

The potential for human exposure via volatilisation of groundwater contaminants into indoor air has been a focus of increasing concern in recent years. At a small number of sites, elevated indoor vapour concentrations have been measured within buildings overlying shallow groundwater contaminated with chlorinated solvents, causing public concern over the potential for similar problems at other corrective action sites. In addition, use of the screening-levelmodel developed by Johnson and Ettinger (1991) for the groundwater-to-indoor-air exposure pathway has suggested that low microgram per litre (ug/L)-range concentrations of either chlorinated or non-chlorinated volatile organic compounds dissolved in groundwater could result in indoor vapour concentrations in excess of applicable risk-based exposure limits. As an alternative screening tool, this paper presents a groundwater mass flux model for evaluation of transport to indoor air. The mass flux model is intended to serve as a highly conservative screening tool that over-predicts groundwater-to-indoor-air mass flux, yet still provides sufficient sensitivity to identify sites for which the groundwater-to-indoor air exposure pathway is not a concern. (orig.)

Isotope and minor element geochemistry of high arsenic groundwater from Hangjinhouqi, the Hetao Plain, Inner Mongolia

International Nuclear Information System (INIS)

Deng Yamin; Wang Yanxin; Ma Teng

2009-01-01

High As groundwater is widely distributed in the northwestern Hetao Plain, an arid region with slow groundwater flow. Arsenic concentration in groundwater ranges from 1 to 1000 μg/L. Most water samples have elevated salinities, with Cl and/or HCO 3 as the dominant anions and Na as the dominant cation. High concentrations of As in shallow aquifers are associated with strongly reducing conditions, as evidenced by high concentrations of dissolved organic C (DOC), NH 4 , dissolved sulfide, arsenite and dissolved CH 4 , and relatively low concentrations of NO 3 - and SO 4 2- . Results of the hydrochemical, and H and O isotope geochemical studies indicate that evapotranspiration is an important process controlling the enrichment of Na and Cl as well as trace elements such as As, B, F and Br in groundwater. In Na-HCO 3 -dominated groundwaters, As, B and F were enriched. Decades of irrigation using Yellow River water has resulted in elevation of the groundwater level, which has accelerated salt accumulation in shallow groundwater and surface soil. In addition, irrigation is responsible for the release of some components from aquifer materials and mixing with saline groundwaters, as indicated by minor element and isotope geochemical data. Used to trace groundwater flow paths, Sr isotope composition also indicates that bedrock weathering is one of the primary sources of As in groundwater in the study area.

Detection of 14C in natural trace organics recovered from groundwater

International Nuclear Information System (INIS)

Murphy, E.; Long, A.; Davis, S.N.; Donahue, D.

1985-01-01

Radiocarbon measurements on dissolved inorganic carbon (DIC) in groundwater have given the authors insight into chemical and hydrological processes occurring in aquifers. Carbon-14 analyses on various dissolved organic carbon (DOC) fractions from groundwater are only starting, but, as is true for DIC 14 C measurements, their significance reaches beyond dating of water and into chemical processes in the aquifer and recharge zone. When combined with information on the chemical character of the DOC, 14 C data may clarify the origin and diagenesis of organic carbon in groundwater. In the past, research into the 14 C has been discouraged by the low concentrations of DOC in groundwater, typically in the μg/l range. The tandem accelerator at the University of Arizona can analyze 14 C in as little as 1 mg of carbon, thus requiring isolation of the DOC from 200 l or less of groundwater. This paper describes the techniques bring used for separation of the DOC in groundwater, some of the data collected, and the significance of these data

Comparison of the hydrogeology and water quality of a ground-water augmented lake with two non-augmented lakes in northwest Hillsborough County, Florida

Science.gov (United States)

Metz, Patricia A.; Sacks, Laura A.

2002-01-01

lakes, which is additional evidence of the limited confinement at Round Lake. A comparison of the water quality and lake-bottom sediments at the three lakes indicate that Round Lake is strongly influenced by the addition of large quantities of calcium-bicarbonate enriched augmentation water. Round Lake had higher alkalinity, pH, calcium and dissolved oxygen concentrations, specific conductance, and water clarity than the two non-augmented lakes. Round Lake was generally saturated to supersaturated with respect to calcite, but was undersaturated when augmentation was low and after high rainfall periods. Calcium carbonate has accumulated in the lake sediments from calcite precipitation, from macrophytes such as Nitella sp., and from the deposition of carbonate-rich mollusk shells, such as Planerbella sp., both of which thrive in the high alkalinity lake water. Lake-bottom sediments and aquatic biota at Round Lake had some of the highest radium-226 activity levels measured in a Florida lake. The high radium-226 levels (27 disintegrations per minute per dry mass) can be atrributed to augmenting the lake with ground water from the Upper Floridan aquifer. Although the ground water has relatively low levels of radium-226 (5.8 disintegrations per minute per liter), the large volumes of ground water added to the lake for more than 30 years have caused radium-226 to accumulate in the sediments and lake biota.The Round Lake basin had higher calcium and bicarbonate concentrations in the surficial aquifer than at the non-augmented lakes, which indicates the lateral leakage of calcium-bicarbonate enriched lake water into the surficial aquifer. Deuterium and oxygen-18 data indicated that water in well nests near the lake consists of as much as 100 percent lake leakage, and water from the augmentation well had a high percentage of recirculated lake water (between 59 and 73 percent lake leakage). The ground water surrounding Round Lake was undersaturated with respect to calcite

Fresh meteoric versus recirculated saline groundwater nutrient inputs into a subtropical estuary

International Nuclear Information System (INIS)

Sadat-Noori, Mahmood; Santos, Isaac R.; Tait, Douglas R.; Maher, Damien T.

2016-01-01

The role of groundwater in transporting nutrients to coastal aquatic systems has recently received considerable attention. However, the relative importance of fresh versus saline groundwater-derived nutrient inputs to estuaries and how these groundwater pathways may alter surface water N:P ratios remains poorly constrained. We performed detailed time series measurements of nutrients in a tidal estuary (Hat Head, NSW, Australia) and used radium to quantify the contribution of fresh and saline groundwater to total surface water estuarine exports under contrasting hydrological conditions (wet and dry season). Tidally integrated nutrient fluxes showed that the estuary was a source of nutrients to the coastal waters. Dissolved inorganic nitrogen (DIN) export was 7-fold higher than the average global areal flux rate for rivers likely due to the small catchment size, surrounding wetlands and high groundwater inputs. Fresh groundwater discharge was dominant in the wet season accounting for up to 45% of total dissolved nitrogen (TDN) and 48% of total dissolved phosphorus (TDP) estuarine exports. In the dry season, fresh and saline groundwater accounted for 21 and 33% of TDN export, respectively. The combined fresh and saline groundwater fluxes of NO_3, PO_4, NH_4, DON, DOP, TDN and TDP were estimated to account for 66, 58, 55, 31, 21, 53 and 47% of surface water exports, respectively. Groundwater-derived nitrogen inputs to the estuary were responsible for a change in the surface water N:P ratio from typical N-limiting conditions to P-limiting as predicted by previous studies. This shows the importance of both fresh and saline groundwater as a source of nutrients for coastal productivity and nutrient budgets of coastal waters. - Highlights: • Groundwater TDN and TDP fluxes account for 53 and 47% of surface water exports. • The estuary DIN export was 7-fold higher than the average global areal flux. • Fresh GW nutrient input dominated the wet season and saline GW the

Elevated concentrations of dissolved Ba, Fe and Mn in a mangrove subterranean estuary: Consequence of sea level rise?

Science.gov (United States)

Sanders, Christian J.; Santos, Isaac R.; Barcellos, Renato; Silva Filho, Emmanoel V.

2012-07-01

Groundwater underlying a mangrove habitat was studied to determine the geochemical nature of Ba, Fe and Mn as related to dissolved organic carbon (DOC), SO4 and salinity (Sepetiba Bay, Brazil). Wells were placed across geobotanic facies and sampled monthly for a year. We observed non-conservative behavior and elevated concentrations of dissolved metals relative to local end-members (i.e., fresh river water and seawater). Average Ba concentrations were near 2000 nM in an area with low salinity (˜5.3). Dissolved Fe (up to 654 μM) was two orders of magnitude greater in fresh groundwater than in the seaward sampling stations. Manganese concentrations were greatest (112 μM) in the high salinity (˜65) zone, being directly influenced by salinity. Groundwater Ba, Fe and Mn showed differing site specific concentrations, likely related to ion exchange processes and redox-controlled cycling along distinct mangrove facies. The results of this work show that metal concentrations are altered relative to conservative mixing between terrestrial and marine endmembers, illustrating the importance of mangrove subterranean estuaries as biogeochemical reactors. Roughly-estimated submarine groundwater discharge-derived dissolved Ba, Fe and Mn fluxes were at least one order of magnitude greater than river-derived fluxes into Sepetiba Bay.

Increased concentrations of potassium in heartwood of trees in response to groundwater contamination

Science.gov (United States)

Vroblesky, Don A.; Yanosky, Thomas M.; Siegel, Frederic R.

1992-03-01

The wood of tuliptrees ( Liriodendron tulipifera L.) growing above groundwater contamination from a hazardous-waste landfill in Maryland contained elevated concentrations of potassium (K). The groundwater contamination also contained elevated concentrations of dissolved K, as well as arsenic (As), cadmium (Cd), chloride (Cl), iron (Fe), manganese (Mn), zinc (Zn), and organic solvents. The dissolved K is derived from disposed smoke munitions. The excess K in the tuliptrees is concentrated in the heartwood, the part of the xylem most depleted in K in trees growing outside of the contamination. These data show that the uptake and translocation of K by tuliptrees can be strongly influenced by the availability of K in groundwater contamination and suggest the utility of this species as an areal indicator of groundwater contamination.

In Situ Groundwater Denitrification in the Riparian Zone of a Short-Rotation Woody Crop Experimental Watershed

Science.gov (United States)

Jeffers, J. B.; Jackson, C. R.; Rau, B.; Pringle, C. M.; Matteson, C.

2017-12-01

The southeastern United States has potential to become a major producer of short rotation woody crops (SRWC) for the production of biofuels, but this will require converting to more intensive forest management practices that will increase nitrate (NO3-) loading and alter nitrogen cycling in nearby freshwater ecosystems. Water quality monitoring in an experimental short-rotation woody crop watershed in the Coastal Plain of South Carolina has shown increased concentrations of NO3- in groundwater but no evidence of increased NO3- in riparian groundwater or surface waters. Forested riparian areas established as streamside management zones (SMZ) are known to act as buffers to surface water bodies by mitigating nutrients. The objectives of this study were to quantify denitrification by measuring dinitrogen (N2) and nitrous oxide (N2O) concentrations along groundwater flow paths and analyze relationships between denitrification estimates, nutrients, and water chemistry parameters. A network of piezometers has been established in the Fourmile Experimental Watershed at the Department of Energy - Savannah River Site. Water samples were collected monthly and were analyzed for concentrations of nutrients (temperature, specific conductivity, dissolved oxygen, pH, dissolved organic carbon) and dissolved gases (N2, Ar, N2O). Preliminary data showed greater dissolved N2O concentrations than dissolved N2 concentrations in groundwater. The ratios of N2O to combined end products of denitrification (N2O / N2O+N2) ranged from 0.33 to 0.99. Mean N2O+N2 concentrations were greater in groundwater samples in the SRWC plot and along the SMZ boundary than along the ephemeral stream within the riparian zone. Correlations between water chemistry parameters and N2 concentrations are indicative of known biogeochemical driving factors of denitrification. Continued monthly sampling will be coupled with analysis of nutrient concentrations (NO3-, NH4+, TN) to help determine transport and processing

Hydrogeologic and geochemical studies of selected natural radioisotopes and barium in groundwater in Illinois. Final report

International Nuclear Information System (INIS)

Gilkeson, R.H.; Cartwright, K.; Cowart, J.B.; Holtzman, R.B.

1983-05-01

Dissolved concentrations of the natural radioisotopes 222 Rn, 226 Ra, 228 Ra, 230 Th, 232 Th, 234 U and 238 U and the element Ba 2+ were investigated in a study of high concentrations of 226 Ra, 228 Ra, and Ba 2+ in groundwater from the Cambrian and Ordovician bedrock of northern Illinois. The high radium and barium concentrations are naturally present in the major aquifers - the sandstone bedrock; therefore, remedial well construction measures will not lower the concentrations. The combined concentrations of 226 Ra and 228 Ra range from 2.3 to 50.2 pCi/L; the majority of analyses exceed the limit in the drinking water regulations of 5.0 pCi/L. The 226 Ra/ 228 Ra activity ratio ranges from 0.2 to 41.0; a 226 Ra analysis has no validity for predicting the 228 Ra concentration. Important controls on dissolved 226 Ra concentrations are secondary U on the sandstone matrix and the ionic strength of groundwater. The distribution of accessory minerals that contain 232 Th is believed to be an important control on dissolved 228 Ra concentrations. Locally the dissolved 226 Ra and 228 Ra concentrations are affected by dissolution-precipitation of secondary barite. Dissolved concentrations of 222 Rn and U are less than proposed drinking water regulations. The extreme enrichment in 234 U that occurs widespread in groundwater from the Cambrian and Ordovician bedrock is unique and problematic. The enrichment may reflect recharge of uranium to the bedrock by glacial processes. Dissolved Ba 2+ concentrations range from 2+ concentrations occur in groundwater that is depleted in dissolved SO 4 2- by anaerobic microbial reactions. A map presents the distribution of Ba 2+ in groundwater from the Cambrian and Ordovician bedrock in northeastern Illinois. 60 references, 13 figures, 3 tables

Dating base flow in streams using dissolved gases and diurnal temperature changes

Science.gov (United States)

Sanford, Ward E.; Casile, Gerolamo C.; Haase, Karl B.

2015-01-01

A method is presented for using dissolved CFCs or SF6 to estimate the apparent age of stream base flow by indirectly estimating the mean concentration of the tracer in the inflowing groundwater. The mean value is estimated simultaneously with the mean residence times of the gas and water in the stream by sampling the stream for one or both age tracers, along with dissolved nitrogen and argon at a single location over a period of approximately 12–14 h. The data are fitted to an equation representing the temporal in-stream gas exchange as it responds to the diurnal temperature fluctuation. The efficacy of the method is demonstrated by collecting and analyzing samples at six different stream locations across parts of northern Virginia, USA. The studied streams drain watersheds with areas of between 2 and 122 km2 during periods when the diurnal stream temperature ranged between 2 and 5°C. The method has the advantage of estimating the mean groundwater residence time of discharge from the watershed to the stream without the need for the collection of groundwater infiltrating to streambeds or local groundwater sampled from shallow observation wells near the stream.

Increased concentrations of potassium in heartwood of trees in response to groundwater contamination

Science.gov (United States)

Vroblesky, D.A.; Yanosky, T.M.; Siegel, F.R.

1992-01-01

The wood of tuliptrees (Liriodendron tulipifera L.) growing above groundwater contamination from a hazardous-waste landfill in Maryland contained elevated concentrations of potassium (K). The groundwater contamination also contained elevated concentrations of dissolved K, as well as arsenic (As), cadmium (Cd), chloride (Cl), iron (Fe), manganese (Mn), zinc (Zn), and organic solvents. The dissolved K is derived from disposed smoke munitions. The excess K in the tuliptrees is concentrated in the heartwood, the part of the xylem most depleted in K in trees growing outside of the contamination. These data show that the uptake and translocation of K by tuliptrees can be strongly influenced by the availability of K in groundwater contamination and suggest the utility of this species as an areal indicator of groundwater contamination. ?? 1992 Springer-Verlag New York Inc.

Geochemical interpretation of groundwaters from Finnsjoen, Sweden

International Nuclear Information System (INIS)

Puigdomenech, I.

1987-01-01

Computer calculations with aqueous speciation models (WATEQ3 and EQ3NR) give a picture of the water-rock interactions. The mineral saturation indices of calcite, strontianite, rhodochrosite, and siderite show that the concentration levels of Ca 2+ , Sr 2+ , Mn 2+ and Fe 2+ are probably fixed by the aqueous carbonate system and its minerals. However, unreasonably high saturation indices of calcite (up to + 1.7) confirm the uncertainties in the pH-values. Computer simulations with the EQ6 code show that CO 2 (g) outgassing/ingassing might have contributed errors in the pH measurements during the sampling procedure. EQ6 simulations also show that mixing of waters from different aquifers might have induced transient over- or undersaturation of carbonate minerals. Equilibrium between groundwaters and fluorite and barite appear to fix the concentrations of F - and Ba 2+ respectively. (orig./DG)

Decoupling of dissolved organic matter patterns between stream and riparian groundwater in a headwater forested catchment

Science.gov (United States)

Bernal, Susana; Lupon, Anna; Catalán, Núria; Castelar, Sara; Martí, Eugènia

2018-03-01

Streams are important sources of carbon to the atmosphere, though knowing whether they merely outgas terrestrially derived carbon dioxide or mineralize terrestrial inputs of dissolved organic matter (DOM) is still a big challenge in ecology. The objective of this study was to investigate the influence of riparian groundwater (GW) and in-stream processes on the temporal pattern of stream DOM concentrations and quality in a forested headwater stream, and whether this influence differed between the leaf litter fall (LLF) period and the remaining part of the year (non-LLF). The spectroscopic indexes (fluorescence index, biological index, humification index, and parallel factor analysis components) indicated that DOM had an eminently protein-like character and was most likely originated from microbial sources and recent biological activity in both stream water and riparian GW. However, paired samples of stream water and riparian GW showed that dissolved organic carbon (DOC) and nitrogen (DON) concentrations as well as the spectroscopic character of DOM differed between the two compartments throughout the year. A simple mass balance approach indicated that in-stream processes along the reach contributed to reducing DOC and DON fluxes by 50 and 30 %, respectively. Further, in-stream DOC and DON uptakes were unrelated to each other, suggesting that these two compounds underwent different biogeochemical pathways. During the LLF period, stream DOC and DOC : DON ratios were higher than during the non-LLF period, and spectroscopic indexes suggested a major influence of terrestrial vegetation on stream DOM. Our study highlights that stream DOM is not merely a reflection of riparian GW entering the stream and that headwater streams have the capacity to internally produce, transform, and consume DOM.

Fresh meteoric versus recirculated saline groundwater nutrient inputs into a subtropical estuary

Energy Technology Data Exchange (ETDEWEB)

Sadat-Noori, Mahmood, E-mail: mahmood.sadat-noori@scu.edu.au [National Marine Science Centre, School of Environment, Science and Engineering, Southern Cross University, Coffs Harbour, NSW (Australia); School of Environment, Science and Engineering, Southern Cross University, Lismore, NSW (Australia); Santos, Isaac R. [National Marine Science Centre, School of Environment, Science and Engineering, Southern Cross University, Coffs Harbour, NSW (Australia); Tait, Douglas R. [National Marine Science Centre, School of Environment, Science and Engineering, Southern Cross University, Coffs Harbour, NSW (Australia); School of Environment, Science and Engineering, Southern Cross University, Lismore, NSW (Australia); Maher, Damien T. [School of Environment, Science and Engineering, Southern Cross University, Lismore, NSW (Australia)

2016-10-01

The role of groundwater in transporting nutrients to coastal aquatic systems has recently received considerable attention. However, the relative importance of fresh versus saline groundwater-derived nutrient inputs to estuaries and how these groundwater pathways may alter surface water N:P ratios remains poorly constrained. We performed detailed time series measurements of nutrients in a tidal estuary (Hat Head, NSW, Australia) and used radium to quantify the contribution of fresh and saline groundwater to total surface water estuarine exports under contrasting hydrological conditions (wet and dry season). Tidally integrated nutrient fluxes showed that the estuary was a source of nutrients to the coastal waters. Dissolved inorganic nitrogen (DIN) export was 7-fold higher than the average global areal flux rate for rivers likely due to the small catchment size, surrounding wetlands and high groundwater inputs. Fresh groundwater discharge was dominant in the wet season accounting for up to 45% of total dissolved nitrogen (TDN) and 48% of total dissolved phosphorus (TDP) estuarine exports. In the dry season, fresh and saline groundwater accounted for 21 and 33% of TDN export, respectively. The combined fresh and saline groundwater fluxes of NO{sub 3}, PO{sub 4}, NH{sub 4}, DON, DOP, TDN and TDP were estimated to account for 66, 58, 55, 31, 21, 53 and 47% of surface water exports, respectively. Groundwater-derived nitrogen inputs to the estuary were responsible for a change in the surface water N:P ratio from typical N-limiting conditions to P-limiting as predicted by previous studies. This shows the importance of both fresh and saline groundwater as a source of nutrients for coastal productivity and nutrient budgets of coastal waters. - Highlights: • Groundwater TDN and TDP fluxes account for 53 and 47% of surface water exports. • The estuary DIN export was 7-fold higher than the average global areal flux. • Fresh GW nutrient input dominated the wet season and

Removal of both dissolved and particulate iron from groundwater

NARCIS (Netherlands)

Teunissen, K.; Abrahamse, A.; Leijssen, H.; Rietveld, L.; Van Dijk, H.

2008-01-01

Iron is the primary source for discolouration problems in the drinking water distribution system. The removal of iron from groundwater is a common treatment step in the production of drinking water. Even when clear water meets the drinking water standards, the water quality in the distribution

STATISTICAL INVESTIGATION OF THE GROUNDWATER SYSTEM IN DARB EL-ARBAEIN, SOUTHWESTERN DESERT, EGYPT

Directory of Open Access Journals (Sweden)

Kashouty Mohamed El

2009-12-01

Full Text Available In Darb El Arbaein, the groundwater is the only water resources. The aquifer system starts from Paleozoic-Mesozoic to Upper Cretaceous sandstone rocks. They overlay the basement rocks and the aquifer is confined. In the present research, the performance of the statistical analyses to classify groundwater samples depending on their chemical characters has been tested. The hydrogeological and hydrogeochemical data of 92 groundwater samples was obtained from the GARPAD authority in northern, central, and southern Darb El Arbaein. A robust classification scheme for partitioning groundwater chemistry into homogeneous groups was an important tool for the characterization of Nubian sandstone aquifer. We test the performance of the many available graphical and statistical methodologies used to classify water samples. R-mode, Q-mode, correlation analysis, and principal component analysis were investigated. All the methods were discussed and compared as to their ability to cluster, ease of use, and ease of interpretation. The correlation investigation clarifies the relationship among the lithology, hydrogeology, and anthropogenic. Factor investigation revealed three factors namely; the evaporation process-agriculturalimpact-lithogenic dissolution, the hydrogeological characteristics of the aquifer system, and the surface meteoric water that rechargethe aquifer system. Two main clusters that subdivided into four sub clusters were identified in groundwater system based on hydrogeological and hydrogeochemical data. They reflect the impact of geomedia, hydrogeology, geographic position, and agricultural wastewater. The groundwater is undersaturated with respect to most selected minerals. The groundwater was supersaturated with respect to iron minerals in northern and southern Darb El Arbaein. The partial pressure of CO2 of the groundwater versus saturation index of calcite shows the gradual change in PCO2 from atmospheric to the present aquifer

Assessment of hydrogeochemistry and environmental isotopes of surface and groundwaters in the Kütahya Plain, Turkey

Science.gov (United States)

Abadi Berhe, Berihu; Erdem Dokuz, Uğur; Çelik, Mehmet

2017-10-01

The aim of the present work is to determine the geochemical processes that control the nature of the groundwater and assess the quality of water for drinking and public health purposes. Surface and groundwater samples of Kütahya plain were analyzed for their physio-chemical and environmental isotope properties. The relative concentrations of the water ions were found to occur in the order of Ca2+>Mg2+>(K+ + Na+) and HCO3->SO42->Cl-. Piper diagram shows that Ca-Mg/Mg-Ca-HCO3 was the dominant water types. Waters in the area were super-saturated with respect to carbonates. However, they were under-saturated with respect to sulphate minerals. The groundwaters had a mean isotopic composition of -67.32 δ2H and -9.72 δ18O and were comparatively lower than surface waters -64.64 δ2H and -9.25 δ18O. Tritium activities in groundwater from the wells ranged from 1.00 to 8.38 TU with a mean value of 4.37 TU. The impact of agricultural practices and poor sanitation conditions is indicated by the positive correlation between K+ - NO3-, K+- NO2- and HCO3- - Cl- ions as well as Na+ and Mg2+ ions with SO42-ion. The groundwater quality of Kütahya plain is influenced by various natural and anthropogenic factors.

Dissolved Nutrients from Submarine Groundwater in Flic en Flac ...

African Journals Online (AJOL)

through a thin blanket of unconsolidated sediment through a fracture system and is concentrated along the ... The lagoon is subjected to diffuse SGD flows which may contribute to its high dissolved nutrient values. ... coastal zone management and similar tropical volcanic lagoonal systems. INTRODUCTION. Lagoons and ...

REE and Y in groundwater in the upper 1.2 km of Proterozoic granitoids (Eastern Sweden) - Assessing the role of composition and origin of groundwaters, geochemistry of fractures, and organic/inorganic aqueous complexation

Science.gov (United States)

Mathurin, Frédéric A.; Åström, Mats E.; Drake, Henrik; Maskenskaya, Olga M.; Kalinowski, Birgitta E.

2014-11-01

Yttrium and rare earth elements (YREEs) are studied in groundwater in the shallow regolith aquifer and the fracture networks of the upper 1.2 km of Paleoproterozoic granitoids in boreal Europe (Laxemar and Forsmark areas, Sweden). The study includes groundwater sampled via a total of 34 shallow boreholes reaching the bottom of the regolith aquifer, and 72 deep boreholes with equipment designed for retrieval of representative groundwater at controlled depths in the fractured bedrock. The groundwater composition differs substantially between regolith and fracture groundwater and between areas, which affects the dissolved YREE features, including concentrations and NASC normalized patterns. In the fresh groundwater in the regolith aquifers, highest YREE concentrations occur (10th and 90th percentile; Laxemar: 4.4-82 μg L-1; Forsmark: 1.9-19 μg L-1), especially in the slightly acidic groundwater (pH: 6.3-7.2 - Laxemar), where the normalized YREE patterns are slightly enriched in light REEs (LaNASC/YNASC: 1.1-2.4). In the recharge areas, where redox potentials of the regolith groundwater is more moderate, negative Ce anomaly (Laxemar: 0.37-0.45; Forsmark: 0.15-0.92) and positive Y anomaly (mainly in Forsmark: 1.0-1.7) are systematically more pronounced than in discharge areas. The significant correlations between the YREE features and dissolved organic carbon, minor elements, and somewhat pH suggest a strong control of humic substances (HSs) together with Al rich colloids and redox sensitive Fe-Mn hydrous precipitates on the dissolved YREE pools. In the bedrock fractures, the groundwater is circumneutral to slightly basic and displays YREE concentrations that are at least one order of magnitude lower than the regolith groundwater, and commonly below detection limit in the deep brackish and saline groundwater, with some exceptions such as La and Y. At intermediate depth (>50 m), where groundwater of meteoric origin percolates, the LaNASC/YNASC values moderately to

Occurrence of phosphorus in groundwater and surface water of northwestern Mississippi

Science.gov (United States)

Welch, Heather L.; Kingsbury, James A.; Coupe, Richard H.

2010-01-01

Previous localized studies of groundwater samples from the Mississippi River Valley alluvial (MRVA) aquifer have demonstrated that dissolved phosphorus concentrations in the aquifer are much higher than the national background concentration of 0.03 milligram per liter (mg/L) found in 400 shallow wells across the country. Forty-six wells screened in the MRVA aquifer in northwestern Mississippi were sampled from June to October 2010 to characterize the occurrence of phosphorus in the aquifer, as well as the factors that might contribute to high dissolved phosphorus concentrations in groundwater. Dissolved phosphorus concentrations ranged from 0.12 to 1.2 mg/L with a median concentration of 0.62 mg/L. The predominant subunit of the MRVA aquifer in northwestern Mississippi is the Holocene alluvium in which median dissolved phosphorus concentrations were higher than the Pleistocene valley trains deposits subunit. Highest phosphorus concentrations occurred in water from wells located along the Mississippi River. A general association between elevated phosphorus concentrations and dissolved iron concentrations suggests that reducing conditions that mobilize iron in the MRVA aquifer also might facilitate transport of phosphorus. Using baseflow separation to estimate the contribution of baseflow to total streamflow, the estimated contribution to the total phosphorus load associated with baseflow at the Tensas River at Tendal, LA, and at the Bogue Phalia near Leland, MS, was 23 percent and 8 percent, respectively. This analysis indicates that elevated concentrations of dissolved phosphorus in the MRVA aquifer could be a possible source of phosphorus to streams during baseflow conditions. However, the fate of phosphorus in groundwater discharge and irrigation return flow to streams is not well understood.

An initial examination of tungsten geochemistry along groundwater flow paths

Science.gov (United States)

Dave, H. B.; Johannesson, K. H.

2008-12-01

Groundwater samples were collected along groundwater flow paths from the Upper Floridan (Florida), Carrizo Sand (Texas), and the Aquia (Maryland) aquifers and analyzed for tungsten (W) concentrations by high- resolution inductively couple plasma mass spectrometry. At each well head, groundwater samples were also analyzed for pH, specific conductance, temperature, alkalinity, dissolved oxygen (DO), oxidation-reduction potential (Eh), dissolved iron speciation, and dissolved sulfide [S(-II)] concentrations. Sediment samples from the Carrizo Sand and Aquia aquifers were also collected and subjected to sequential extractions to provide additional insights into the solid-phase speciation of W in these aquifers. Tungsten concentrations varied along the groundwater flow paths chiefly in response to changing pH, and to a lesser extent, variations in the redox conditions. For groundwater from the Carrizo Sand aquifer, W ranges between 3.64 and 1297 pmol/kg, exhibiting the lowest values proximal to the recharge zone. Tungsten concentrations progressively increase along the flow path, reaching 1297 pmol/kg in the sulfidic groundwaters located approximately 60 km downgradient from the recharge area. Tungsten is strongly correlated with S(-II) concentrations and pH in Carrizo groundwaters (r = 0.95 and 0.78, respectively). Within the Aquia aquifer, however, W generally occurs at lower concentrations than the Carrizo (14 to 184 pmol/kg; mean = 80 pmol/kg), and shows no systematic trends along the flow path (e.g., r = 0.08 and 0.4 for W vs. S(-II) and pH, respectively). Our data are consistent with the increase in W concentrations in Carrizo groundwaters reflecting, in part, pH-related desorption, which has been shown to be substantial for pH greater than 8. Moreover, because of the broad similarities in the chemistry of W and Mo, which forms thiomolybdates in sulfidic waters, we suggest that thiotungstate complexes may form in sulfidic groundwaters, thus partially explaining the

Flourescence Humic Substances in Arsenic Contaminated Groundwater of Bangladesh

Directory of Open Access Journals (Sweden)

SHAFI M. TAREQ

2012-06-01

Full Text Available In the past, only arsenic (As concentrations in groundwater of Bangladesh were considered as having direct effects on the epidemical degrees of different types of diseases including arsenicosis, but the results of the present investigation indicated that fluorescence humic substance (HS is also an important component of dissolved organic matter in groundwater of Bangladesh. Therefore, it is suspected that both fluorescent HS and As in groundwater may have effects on the biological toxicity. The evidence of presence of high fluorescent HS and As in groundwater of Faridpur supports the above synergistic effect. The spatial distribution of fluorescence HS and As in groundwater of Faridpur indicated that the variations may be related to local hydrogeological conditions.

Measurement of dissolved Cs-137 in stream water, soil water and groundwater at Headwater Forested Catchment in Fukushima after Fukushima Dai-ichi Nuclear Power Plant Accident

Science.gov (United States)

Iwagami, Sho; Tsujimura, Maki; Onda, Yuichi; Sakakibara, Koichi; Konuma, Ryohei; Sato, Yutaro

2016-04-01

Radiocesium migration from headwater forested catchment is important perception as output from the forest which is also input to the subsequent various land use and downstream rivers after Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident. In this study, dissolved Cs-137 concentration of stream water, soil water and groundwater were measured. Observations were conducted at headwater catchment in Yamakiya district, located 35 km northwest of FDNPP from April 2014 to November 2015. Stream water discharge was monitored and stream water samples were taken at main channel and sub channel. Stream water discharge was monitored by combination of parshallflume and v-notch weir. Stream water was sampled manually at steady state condition in 3-4 month interval and also intense few hours interval sampling were conducted during rainfall events using automated water sampler. Around the sub channel, it is found that there is a regularly saturated area at the bottom of the slope, temporary saturated area which saturate during the rainy season in summer and regularly dry area. 6 interval cameras were installed to monitor the changing situation of saturated area. Suction lysimeters were installed at three areas (regularly saturated area, temporary saturated area and dry area) for sampling soil water in depth of 0.1 m and 0.3 m. Boreholes were installed at three points along the sub channel. Three boreholes with depth of 3 m, 5 m and 10 m were installed at temporary saturated area, 20 m upstream of sub channel weir. Another three boreholes with depth of 3 m, 5 m and 10 m were installed at dry area, 40 m upstream of sub channel weir. And a borehole with depth of 20 m was installed at ridge of sub catchment, 52 m upstream of sub channel weir. Groundwater was sampled by electrically powered pump and groundwater level was monitored. Also suction-free lysimeter was installed at temporary saturated area for sampling the near surface subsurface water. Soil water samples were collected

Modeled Sources, Transport, and Accumulation of Dissolved Solids in Water Resources of the Southwestern United States.

Science.gov (United States)

Anning, David W

2011-10-01

Information on important source areas for dissolved solids in streams of the southwestern United States, the relative share of deliveries of dissolved solids to streams from natural and human sources, and the potential for salt accumulation in soil or groundwater was developed using a SPAtially Referenced Regressions On Watershed attributes model. Predicted area-normalized reach-catchment delivery rates of dissolved solids to streams ranged from Salton Sea accounting unit.

Deep groundwater redox reactions in the Palmottu uranium deposit: The role of uranium and iron in these processes

International Nuclear Information System (INIS)

Bruno, J.; Cera, E.; Duro, L.; Ahonen, L.

1996-12-01

The reduction oxidation properties of the deep bedrock and groundwater are important geochemical factors with respect to the chemical stability of the multibarrier system, which isolates the disposed nuclear fuel from biosphere. In the report are described the results of the redox experiments carried out in the field using the natural groundwaters of Palmottu, in Nummi-Pusula, Finland. The experiments include (1) measurements of natural water redox potential values during four to eight hours continuous pumping; (2) monitoring of the redox-potential response to an artificial change of pH of the groundwater. Separate tests were made in iron and uranium-rich groundwaters, respectively. The data of the field experiments were used in the redox-modelling of the iron and uranium systems. In accordance with earlier knowledge, it was showed that dissolved iron is an important redox electrolyte in natural waters, at least at concentration levels of milligrams per liter. However, a striking observation was that in the absence of dissolved iron dissolved uranium (in concentrations of about 200 nM or more) seems to be able to give nernstian response on platinum electrode in acid/base titrations. The effective redox properties of the bedrock-groundwater system depend on the availability and reactivity of solid phases able to exchange electrons with dissolved redox electrolytes. The present results indicate that, in the bedrock/groundwater system of the Palmottu uranium mineralization, uranium minerals are important redox buffers. (orig.) (refs.)

an approach to estimate total dissolved solids in groundwater using

African Journals Online (AJOL)

resistivities of the aquifer delineated were subsequently used to estimate TDS in groundwater which was correlated with those ... the concentrations of these chemical constituents in the ..... TDS determined by water analysis varied between 17.

Cyclic metal migration in a groundwater stream

International Nuclear Information System (INIS)

Goerlich, W.; Portmann, W.; Wernli, C.; Linder, P.; Burkart, W.

1988-04-01

The behaviour of dissolved (<0.45 μm) inorganic species (e.g. metals, anions), and changes in relevant properties of polluted river water during infiltration into adjacent groundwater are investigated. Water from the river and from several wells is analyzed for temporal and spacial changes. For many of the measured quantities a pronounced annual cycle is observed. The temperature differences between summer and winter influence biological activity. Growth and degradation of organic material lead to drastic changes in pH and redox conditions in the near infiltration field. During summer, under relatively anoxic conditions, manganese oxides/hydroxides dissolve. In winter, the higher concentration of dissolved oxygen induce reprecipitation of manganese. Trace metal mobility (e.g. Cu, Zn, Cd) is influenced by these annual variations. In the river, daily cycles are observed for many of the measured quantities. These short term variations are induced by photosynthesis and respiration of aquatic biota. The cyclic behaviour disappears during the early stage of infiltration. The changes between river and groundwater can be modelled by a combination of simplified electron transfer and weathering reactions. (author) 11 refs., 5 figs

Earthquake chemical precursors in groundwater: a review

Science.gov (United States)

Paudel, Shukra Raj; Banjara, Sushant Prasad; Wagle, Amrita; Freund, Friedemann T.

2018-03-01

We review changes in groundwater chemistry as precursory signs for earthquakes. In particular, we discuss pH, total dissolved solids (TDS), electrical conductivity, and dissolved gases in relation to their significance for earthquake prediction or forecasting. These parameters are widely believed to vary in response to seismic and pre-seismic activity. However, the same parameters also vary in response to non-seismic processes. The inability to reliably distinguish between changes caused by seismic or pre-seismic activities from changes caused by non-seismic activities has impeded progress in earthquake science. Short-term earthquake prediction is unlikely to be achieved, however, by pH, TDS, electrical conductivity, and dissolved gas measurements alone. On the other hand, the production of free hydroxyl radicals (•OH), subsequent reactions such as formation of H2O2 and oxidation of As(III) to As(V) in groundwater, have distinctive precursory characteristics. This study deviates from the prevailing mechanical mantra. It addresses earthquake-related non-seismic mechanisms, but focused on the stress-induced electrification of rocks, the generation of positive hole charge carriers and their long-distance propagation through the rock column, plus on electrochemical processes at the rock-water interface.

Hydrogeology, simulated ground-water flow, and ground-water quality, Wright-Patterson Air Force Base, Ohio

Science.gov (United States)

Dumouchelle, D.H.; Schalk, C.W.; Rowe, G.L.; De Roche, J.T.

1993-01-01

percent of the total ground-water flow in the study area. Ground waters in the vicinity of Wright-Patterson Air Force Base can be classified into two compositional groups on the basis of their chemical composition: calcium magnesium bicarbonate-type and sodium chloride-type waters. Calcium magnesium bicarbonate-type waters are found in the glacial deposits and the Brassfield Limestone, whereas the sodium chloride waters are exclusively associated with the shales. Equilibrium speciation calculations indicate that ground water of the glacial drift aquifer is in equilibrium with calcite, dolomite, and chalcedony, but is undersaturated with respect to gypsum and fluorite. Waters from the shales are slightly supersaturated with respect to calcite, dolomite, and siderite but are undersaturated with respect to chalcedony. Simple-mass balance calculations treating boron as a conservative species indicate that little (origin for all ground water beneath Wright-Patterson Air Force Base, but the data were inconclusive with respect to identification of distinct isotopic differences between water collected from the glacial drift and bedrock aquifers. Tritium concentrations used to distinguish waters having a pre-and post-1953 recharge component indicate that most water entered the glacial drift aquifer after 1953. This finding indicates that recharge from shallow to deep parts (greater than 150 feet) of the aquifer takes place over time intervals of a few years or decades. However, the fact that some deep parts of the glacial aquifer did not contain measurable tritium indicates that ground-water flow from recharge zones to these parts of the aquifer takes decades or longer.

Evaluation of high-frequency mean streamwater transit-time estimates using groundwater age and dissolved silica concentrations in a small forested watershed

Science.gov (United States)

Peters, Norman E.; Burns, Douglas A.; Aulenbach, Brent T.

2014-01-01

Many previous investigations of mean streamwater transit times (MTT) have been limited by an inability to quantify the MTT dynamics. Here, we draw on (1) a linear relation (r 2 = 0.97) between groundwater 3H/3He ages and dissolved silica (Si) concentrations, combined with (2) predicted streamwater Si concentrations from a multiple-regression relation (R 2 = 0.87) to estimate MTT at 5-min intervals for a 23-year time series of streamflow [water year (WY) 1986 through 2008] at the Panola Mountain Research Watershed, Georgia. The time-based average MTT derived from the 5-min data was ~8.4 ± 2.9 years and the volume-weighted (VW) MTT was ~4.7 years for the study period, reflecting the importance of younger runoff water during high flow. The 5-min MTTs are normally distributed and ranged from 0 to 15 years. Monthly VW MTTs averaged 7.0 ± 3.3 years and ranged from 4 to 6 years during winter and 8–10 years during summer. The annual VW MTTs averaged 5.6 ± 2.0 years and ranged from ~5 years during wet years (2003 and 2005) to >10 years during dry years (2002 and 2008). Stormflows are composed of much younger water than baseflows, and although stormflow only occurs ~17 % of the time, this runoff fraction contributed 39 % of the runoff during the 23-year study period. Combining the 23-year VW MTT (including stormflow) with the annual average baseflow for the period (~212 mm) indicates that active groundwater storage is ~1,000 mm. However, the groundwater storage ranged from 1,040 to 1,950 mm using WY baseflow and WY VW MTT. The approach described herein may be applicable to other watersheds underlain by granitoid bedrock, where weathering is the dominant control on Si concentrations in soils, groundwater, and streamwater.

Catchment tracers reveal discharge, recharge and sources of groundwater-borne pollutants in a novel lake modelling approach

Science.gov (United States)

Kristensen, Emil; Madsen-Østerbye, Mikkel; Massicotte, Philippe; Pedersen, Ole; Markager, Stiig; Kragh, Theis

2018-02-01

Groundwater-borne contaminants such as nutrients, dissolved organic carbon (DOC), coloured dissolved organic matter (CDOM) and pesticides can have an impact the biological quality of lakes. The sources of pollutants can, however, be difficult to identify due to high heterogeneity in groundwater flow patterns. This study presents a novel approach for fast hydrological surveys of small groundwater-fed lakes using multiple groundwater-borne tracers. Water samples were collected from the lake and temporary groundwater wells, installed every 50 m within a distance of 5-45 m to the shore, were analysed for tracer concentrations of CDOM, DOC, total dissolved nitrogen (TDN, groundwater only), total nitrogen (TN, lake only), total dissolved phosphorus (TDP, groundwater only), total phosphorus (TP, lake only), δ18O / δ16O isotope ratios and fluorescent dissolved organic matter (FDOM) components derived from parallel factor analysis (PARAFAC). The isolation of groundwater recharge areas was based on δ18O measurements and areas with a high groundwater recharge rate were identified using a microbially influenced FDOM component. Groundwater discharge sites and the fractions of water delivered from the individual sites were isolated with the Community Assembly via Trait Selection model (CATS). The CATS model utilized tracer measurements of TDP, TDN, DOC and CDOM from the groundwater samples and related these to the tracer measurements of TN, TP, DOC and CDOM in the lake. A direct comparison between the lake and the inflowing groundwater was possible as degradation rates of the tracers in the lake were taken into account and related to a range of water retention times (WRTs) of the lake (0.25-3.5 years in 0.25-year increments). These estimations showed that WRTs above 2 years required a higher tracer concentration of inflowing water than found in any of the groundwater wells around the lake. From the estimations of inflowing tracer concentration, the CATS model isolated

The interaction between surface water and groundwater and its ...

Indian Academy of Sciences (India)

Surface water; groundwater; stable isotopes; water quality; Second Songhua River basin. .... The total dissolved solid (TDS) was calculated by the con- centrations of major ions in ...... evaluating water quality management effectiveness; J.

Evaluation on changes caused by volcanic activities in the groundwater environment as a natural barrier for the HLW disposal. Literature survey and groundwater observation conducted at Mt. Iwate

International Nuclear Information System (INIS)

Mahara, Yasunori; Nakata, Eiji; Tanaka, Kazuhiro

2000-01-01

It is very important in the site characterization for the HLW disposal to understand changes in geochemical performances caused by volcanic activities in the groundwater environment as the natural barrier. The various effects and its magnitude of changes were listed up and were filed from literature surveys of the correlation between volcanic activities and hydrological can geochemical changes (e.g. water temperature, water pressure, water level, dissolved gas concentration of He and Rn, isotopic ratio of He, and chloride concentration) in volcanic aquifer. However, it is difficult to evaluate the magnitude of impacts, which volcanic activities will give to the groundwater environment in the natural barrier, through only the literature surveys. We have started monitoring of groundwater level and changes in groundwater quality, since volcanic activities have enhanced at Mt. Iwate from June in 1998. Judging from variation of isotopic ratio of dissolved He in groundwater, a prompt and sharp signals indicating volcanic activities will easily be found in shallow groundwater and discharged ponds. On the other hands, geochemical conditions in deep groundwater surroundings from some 100 m to 1000 m deep will be very stable, if the area being more than 5 km apart from the volcanic active center. Consequently, our observed results suggest that the groundwater environment which is not directly disturbed by the underground magmatic activities spreads under the area that is connected to trench side of the volcanic front. (author)

Uranium isotopes in groundwater occurring at Amazonas State, Brazil

International Nuclear Information System (INIS)

Luiz da Silva, Márcio; Bonotto, Daniel Marcos

2015-01-01

This paper reports the behavior of the dissolved U-isotopes 238 U and 234 U in groundwater providing from 15 cities in Amazonas State, Brazil. The isotope dilution technique accompanied by alpha spectrometry were utilized for acquiring the U content and 234 U/ 238 U activity ratio (AR) data, 0.01–1.4 µg L −1 and 1.0–3.5, respectively. These results suggest that the water is circulating in a reducing environment and leaching strata containing minerals with low uranium concentration. A tendency to increasing ARs values following the groundwater flow direction is identified in Manaus city. The AR also increases according to the SW–NE directions: Uarini→Tefé; Manacapuru→Manaus; Presidente Figueiredo→São Sebastião do Uatumã; and Boa Vista do Ramos→Parintins. Such trends are possibly related to several factors, among them the increasing acid character of the waters. The waters analyzed are used for human consumption and the highest dissolved U content is much lower than the maximum established by the World Health Organization. Therefore, in view of this radiological parameter they can be used for drinking purposes. - Highlights: • U-isotopes data in important aquifer systems in Amazon area. • Application of the U-isotopes data to investigate the groundwater flow direction. • Evaluation of the drinking-water quality in terms of dissolved uranium

A review of single-sample-based models and other approaches for radiocarbon dating of dissolved inorganic carbon in groundwater

Science.gov (United States)

Han, L. F; Plummer, Niel

2016-01-01

Numerous methods have been proposed to estimate the pre-nuclear-detonation 14C content of dissolved inorganic carbon (DIC) recharged to groundwater that has been corrected/adjusted for geochemical processes in the absence of radioactive decay (14C0) - a quantity that is essential for estimation of radiocarbon age of DIC in groundwater. The models/approaches most commonly used are grouped as follows: (1) single-sample-based models, (2) a statistical approach based on the observed (curved) relationship between 14C and δ13C data for the aquifer, and (3) the geochemical mass-balance approach that constructs adjustment models accounting for all the geochemical reactions known to occur along a groundwater flow path. This review discusses first the geochemical processes behind each of the single-sample-based models, followed by discussions of the statistical approach and the geochemical mass-balance approach. Finally, the applications, advantages and limitations of the three groups of models/approaches are discussed.The single-sample-based models constitute the prevailing use of 14C data in hydrogeology and hydrological studies. This is in part because the models are applied to an individual water sample to estimate the 14C age, therefore the measurement data are easily available. These models have been shown to provide realistic radiocarbon ages in many studies. However, they usually are limited to simple carbonate aquifers and selection of model may have significant effects on 14C0 often resulting in a wide range of estimates of 14C ages.Of the single-sample-based models, four are recommended for the estimation of 14C0 of DIC in groundwater: Pearson's model, (Ingerson and Pearson, 1964; Pearson and White, 1967), Han & Plummer's model (Han and Plummer, 2013), the IAEA model (Gonfiantini, 1972; Salem et al., 1980), and Oeschger's model (Geyh, 2000). These four models include all processes considered in single-sample-based models, and can be used in different ranges of

The soil organic carbon content of anthropogenically altered organic soils effects the dissolved organic matter quality, but not the dissolved organic carbon concentrations

Science.gov (United States)

Frank, Stefan; Tiemeyer, Bärbel; Bechtold, Michel; Lücke, Andreas; Bol, Roland

2016-04-01

Dissolved organic carbon (DOC) is an important link between terrestrial and aquatic ecosystems. This is especially true for peatlands which usually show high concentrations of DOC due to the high stocks of soil organic carbon (SOC). Most previous studies found that DOC concentrations in the soil solution depend on the SOC content. Thus, one would expect low DOC concentrations in peatlands which have anthropogenically been altered by mixing with sand. Here, we want to show the effect of SOC and groundwater level on the quantity and quality of the dissolved organic matter (DOM). Three sampling sites were installed in a strongly disturbed bog. Two sites differ in SOC (Site A: 48%, Site B: 9%) but show the same mean annual groundwater level of 15 and 18 cm below ground, respectively. The SOC content of site C (11%) is similar to Site B, but the groundwater level is much lower (-31 cm) than at the other two sites. All sites have a similar depth of the organic horizon (30 cm) and the same land-use (low-intensity sheep grazing). Over two years, the soil solution was sampled bi-weekly in three depths (15, 30 and 60 cm) and three replicates. All samples were analyzed for DOC and selected samples for dissolved organic nitrogen (DON) and delta-13C and delta-15N. Despite differences in SOC and groundwater level, DOC concentrations did not differ significantly (A: 192 ± 62 mg/L, B: 163 ± 55 mg/L and C: 191 ± 97 mg/L). At all sites, DOC concentrations exceed typical values for peatlands by far and emphasize the relevance even of strongly disturbed organic soils for DOC losses. Individual DOC concentrations were controlled by the temperature and the groundwater level over the preceding weeks. Differences in DOM quality were clearer. At site B with a low SOC content, the DOC:DON ratio of the soil solution equals the soil's C:N ratio, but the DOC:DON ratio is much higher than the C:N ratio at site A. In all cases, the DOC:DON ratio strongly correlates with delta-13C. There is no

Groundwater quality and hydrochemical properties of Al-Ula Region, Saudi Arabia.

Science.gov (United States)

Toumi, Naji; Hussein, Belal H M; Rafrafi, Sarra; El Kassas, Neama

2015-03-01

Groundwater quality monitoring is one of the most important aspects in groundwater studies in arid environments particularly in developing countries, like Saudi Arabia, due to the fast population growth and the expansion of irrigated agriculture and industrial uses. Groundwater samples have been collected from eight locations in Al-Ula in Saudi Arabia during June 2012 and January 2013 in order to investigate the hydrochemical characteristics and the groundwater quality and to understand the sources of dissolved ions. Physicochemical parameters of groundwater such as electrical conductivity, pH, total dissolved solid, and major cations and anions were determined. Chloride was found to be the dominant anion followed by HCO(-) 3 and SO4 (2-). Groundwater of the study area is characterized by the dominance of alkaline earths (Ca(2+) + Mg(2+)) over alkali metals (Na(+) + K(+)). The analytical results show that the groundwater is generally moderately hard and slightly alkaline in nature. The binary relationships of the major ions reveal that water quality of the Al-Ula region is mainly controlled by rock weathering, evaporation, and ion exchange reactions. Piper diagram was constructed to identify hydrochemical facies, and it was found that majority of the samples belong to Ca-Cl and mixed Ca-Mg-Cl facies. Chemical indices like chloro-alkali indices, sodium adsorption ratio, percentage of sodium, residual sodium carbonate, and permeability index were calculated. Also, the results show that the chemical composition of groundwater sources of Al-Ula is strongly influenced by lithology of country rocks rather than anthropogenic activities.

Changes in groundwater chemistry before two consecutive earthquakes in Iceland

KAUST Repository

Skelton, Alasdair

2014-09-21

Groundwater chemistry has been observed to change before earthquakes and is proposed as a precursor signal. Such changes include variations in radon count rates1, 2, concentrations of dissolved elements3, 4, 5 and stable isotope ratios4, 5. Changes in seismic wave velocities6, water levels in boreholes7, micro-seismicity8 and shear wave splitting9 are also thought to precede earthquakes. Precursor activity has been attributed to expansion of rock volume7, 10, 11. However, most studies of precursory phenomena lack sufficient data to rule out other explanations unrelated to earthquakes12. For example, reproducibility of a precursor signal has seldom been shown and few precursors have been evaluated statistically. Here we analyse the stable isotope ratios and dissolved element concentrations of groundwater taken from a borehole in northern Iceland between 2008 and 2013. We find that the chemistry of the groundwater changed four to six months before two greater than magnitude 5 earthquakes that occurred in October 2012 and April 2013. Statistical analyses indicate that the changes in groundwater chemistry were associated with the earthquakes. We suggest that the changes were caused by crustal dilation associated with stress build-up before each earthquake, which caused different groundwater components to mix. Although the changes we detect are specific for the site in Iceland, we infer that similar processes may be active elsewhere, and that groundwater chemistry is a promising target for future studies on the predictability of earthquakes.

Hydrogeochemical quality and suitability studies of groundwater in northern Bangladesh.

Science.gov (United States)

Islam, M J; Hakim, M A; Hanafi, M M; Juraimi, Abdul Shukor; Aktar, Sharmin; Siddiqa, Aysha; Rahman, A K M Shajedur; Islam, M Atikul; Halim, M A

2014-07-01

Agriculture, rapid urbanization and geochemical processes have direct or indirect effects on the chemical composition of groundwater and aquifer geochemistry. Hydro-chemical investigations, which are significant for assessment of water quality, were carried out to study the sources of dissolved ions in groundwater of Dinajpur district, northern Bangladesh. The groundwater samplish were analyzed for physico-chemical properties like pH, electrical conductance, hardness, alkalinity, total dissolved solids and Ca2+, Mg2+, Na+, K+, CO3(2-), HCO3(-), SO4(2-) and Cl- ions, respectively. Based on the analyses, certain parameters like sodium adsorption ratio, soluble sodium percentage, potential salinity, residual sodium carbonate, Kelly's ratio, permeability index and Gibbs ratio were also calculated. The results showed that the groundwater of study area was fresh, slightly acidic (pH 5.3-6.4) and low in TDS (35-275 mg I(-1)). Ground water of the study area was found suitable for irrigation, drinking and domestic purposes, since most of the parameters analyzed were within the WHO recommended values for drinking water. High concentration of NO3- and Cl- was reported in areas with extensive agriculture and rapid urbanization. Ion-exchange, weathering, oxidation and dissolution of minerals were major geochemical processes governing the groundwater evolution in study area. Gibb's diagram showed that all the samples fell in the rock dominance field. Based on evaluation, it is clear that groundwater quality of the study area was suitable for both domestic and irrigation purposes.

Changes in groundwater chemistry before two consecutive earthquakes in Iceland

KAUST Repository

Skelton, Alasdair; André n, Margareta; Kristmannsdó ttir, Hrefna; Stockmann, Gabrielle; Mö rth, Carl-Magnus; Sveinbjö rnsdó ttir, Á rny; Jonsson, Sigurjon; Sturkell, Erik; Guð rú nardó ttir, Helga Rakel; Hjartarson, Hreinn; Siegmund, Heike; Kockum, Ingrid

2014-01-01

Groundwater chemistry has been observed to change before earthquakes and is proposed as a precursor signal. Such changes include variations in radon count rates1, 2, concentrations of dissolved elements3, 4, 5 and stable isotope ratios4, 5. Changes in seismic wave velocities6, water levels in boreholes7, micro-seismicity8 and shear wave splitting9 are also thought to precede earthquakes. Precursor activity has been attributed to expansion of rock volume7, 10, 11. However, most studies of precursory phenomena lack sufficient data to rule out other explanations unrelated to earthquakes12. For example, reproducibility of a precursor signal has seldom been shown and few precursors have been evaluated statistically. Here we analyse the stable isotope ratios and dissolved element concentrations of groundwater taken from a borehole in northern Iceland between 2008 and 2013. We find that the chemistry of the groundwater changed four to six months before two greater than magnitude 5 earthquakes that occurred in October 2012 and April 2013. Statistical analyses indicate that the changes in groundwater chemistry were associated with the earthquakes. We suggest that the changes were caused by crustal dilation associated with stress build-up before each earthquake, which caused different groundwater components to mix. Although the changes we detect are specific for the site in Iceland, we infer that similar processes may be active elsewhere, and that groundwater chemistry is a promising target for future studies on the predictability of earthquakes.

Characterization of colloids in groundwater

International Nuclear Information System (INIS)

Kim, J.I.; Buckau, G.; Klenze, R.

1987-07-01

Natural colloids in the Gorleben aquifer systems have been investigated as for their chemical composition, quantification and size distribution. Humic substances appear to be the major organic materials in these groundwaters, generating humic colloids which are analysed to be humic acid (and fulvic acid) loaded with a large number of trace heavy metal ions. These metal ions include natural homologues of actinides and some fission products in trivalent, tetravalent and hexavalent state. Concentrations of trivalent and tetravalent heavy metal ions are linearly correlated with the dissolved organic carbon (DDC) concentration in different groundwaters. The DOC is found to be present as humic colloids. The Am 3+ ions introduced in such a groundwater readily undergo the generation of its pseudocolloids through sorption or ion exchange reactions with humic colloids. The chemical behaviour of Am(III), being similar to the trivalent metal ions, e.g. Fe 3+ , REE etc. found in natural colloids, has been investigated by laser induced photoacoustic spectroscopy (LPAS). Groundwaters from Ispra, Markham Clinton and Felslabor Grimsel. Bidistilled water and one of Gorleben groundwaters, Gohy 1011, are taken for the purpose of comparison. This groundwater contains the least amount of natural colloids of all Gorleben groundwaters hitherto investigated. An indirect quantification is made by comparison of the LPAS results with experiment from Latex solution. (orig./IRB)

Hydrochemical and isotopic characteristics of groundwater in the northeastern Tennger Desert, northern China

Science.gov (United States)

Wang, Liheng; Dong, Yanhui; Xu, Zhifang; Qiao, Xiaojuan

2017-12-01

Groundwater is typically the only water source in arid regions, and its circulation processes should be better understood for rational resource exploitation. Stable isotopes and major ions were investigated in the northeastern Tengger Desert, northern China, to gain insights into groundwater recharge and evolution. In the northern mountains, Quaternary unconsolidated sediments, exposed only in valleys between hills, form the main aquifer, which is mainly made of aeolian sand and gravel. Most of the mountain groundwater samples plot along the local meteoric water line (LMWL), with a more depleted signature compared to summer precipitation, suggesting that mountain groundwater was recharged by local precipitation during winter. Most of the groundwater was fresh, with total dissolved solids less than 1 g/L; dominant ions are Na+, SO4 2- and Cl-, and all mineral saturation indices are less than zero. Evaporation, dissolution and cation exchange are the major hydrogeochemical processes. In the southern plains, however, the main aquifers are sandstone. The linear regression line of δD and δ 18O of groundwater parallels the LMWL but the intercept is lower, indicating that groundwater in the plains has been recharged by ancient precipitation rather than modern. Both calcite and dolomite phases in the plains groundwater are close to saturation, while gypsum and halite can still be dissolved into the groundwater. Different recharge mechanisms occur in the northern mountains and the southern plains, and the hydraulic connection between them is weak. Because of the limited recharge, groundwater exploitation should be limited as much as possible.

Groundwater-derived nutrient inputs to the Upper Gulf of Thailand

Science.gov (United States)

Burnett, William C.; Wattayakorn, Gullaya; Taniguchi, Makoto; Dulaiova, Henrieta; Sojisuporn, Pramot; Rungsupa, Sompop; Ishitobi, Tomotoshi

2007-01-01

We report here the first direct measurements of nutrient fluxes via groundwater discharge into the Upper Gulf of Thailand. Nutrient and standard oceanographic surveys were conducted during the wet and dry seasons along the Chao Phraya River, Estuary and out into the Upper Gulf of Thailand. Additional measurements in selected near-shore regions of the Gulf included manual and automatic seepage meter deployments, as well as nutrient evaluations of seepage and coastal waters. The river transects characterized the distribution of biogeochemical parameters in this highly contaminated urban environment. Seepage flux measurements together with nutrient analyses of seepage fluids were used to estimate nutrient fluxes via groundwater pathways for comparison to riverine fluxes. Our findings show that disseminated seepage of nutrient-rich mostly saline groundwater into the Upper Gulf of Thailand is significant. Estimated fluxes of dissolved inorganic nitrogen (DIN) supplied via groundwater discharge were 40-50% of that delivered by the Chao Phraya River, inorganic phosphate was 60-70%, and silica was 15-40%. Dissolved organic nitrogen (DON) and phosphorus (DOP) groundwater fluxes were also high at 30-40% and 30-130% of the river inputs, respectively. These observations are especially impressive since the comparison is being made to the river that is the largest source of fresh water into the Gulf of Thailand and flows directly through the megacity of Bangkok with high nutrient loadings from industrial and domestic sources.

Microbiology of Olkiluoto Groundwater 2004 - 2006

International Nuclear Information System (INIS)

Pedersen, K.

2008-02-01

The microbiology of shallow and deep groundwater in Olkiluoto, Finland, was analysed for almost three years from 2004 to 2006. The extensive sampling and analysis programme produced a substantial database, including 60 analytical datasets on the microbiology of Olkiluoto groundwater, which is described and interpreted here. One part of this database comprises 39 complete analytical datasets on microbiology, chemistry, and dissolved gas composition assembled on four sampling campaigns from measurements from 16 shallow observation tubes and boreholes ranging in depth from 3.5 to 24.5 m. The second part of the database contains 21 datasets on microbiology and chemistry covering 13 deep boreholes ranging in depth from 35 to 450 m. In addition, the database contains 33 completed analyses of gas covering 14 deep boreholes ranging in depth from 40 to 742 m. Most of these analyses were completed before the onset of ONKALO construction, and the remaining samples were collected before ONKALO construction had extended below a depth of 100 m; therefore, this dataset captures the undisturbed conditions before the building of ONKALO. Shallow groundwater in Olkiluoto contained dissolved oxygen at approximately 10% or less of saturation. The presence of aerobic and anaerobic microorganisms, including methane-oxidizing bacteria, has been documented. The data confirm earlier suggested processes of oxygen reduction in the shallow part of the bedrock. These microbial processes reduce intruding oxygen in the shallow groundwater using dissolved organic carbon and methane as the main electron donors. Microbiological and geochemical data strongly suggest that the anaerobic microbial oxidation of methane (ANME) is active at a depth down to approximately 300 m in Olkiluoto, as has been suggested previously, based on interpretations of geochemical data. However, proof of the presence and activity of ANME microorganisms is needed before the existence of active ANME processes in Olkiluoto

Volcanic degassing at Somma-Vesuvio (Italy) inferred by chemical and isotopic signatures of groundwater

Energy Technology Data Exchange (ETDEWEB)

Caliro, S. [Osservatorio Vesuviano sezione di Napoli dell' Istituto, Nazionale Geofisica Vulcanologia, Via Diocleziano 328, 80124 Naples (Italy)]. E-mail: caliro@ov.ingv.it; Chiodini, G. [Osservatorio Vesuviano sezione di Napoli dell' Istituto, Nazionale Geofisica Vulcanologia, Via Diocleziano 328, 80124 Naples (Italy); Avino, R. [Osservatorio Vesuviano sezione di Napoli dell' Istituto, Nazionale Geofisica Vulcanologia, Via Diocleziano 328, 80124 Naples (Italy); Cardellini, C. [Dipartimento di Scienze della Terra, Universita di Perugia (Italy); Frondini, F. [Dipartimento di Scienze della Terra, Universita di Perugia (Italy)

2005-06-15

A geochemical model is proposed for water evolution at Somma-Vesuvio, based on the chemical and isotopic composition of groundwaters, submarine gas emission and chemical composition of the dissolved gases. The active degassing processes, present in the highest part of the volcano edifice, strongly influence the groundwater evolution. The geological-volcanological setting of the volcano forces the waters infiltrating at Somma-Vesuvio caldera, enriched in volcanic gases, to flow towards the southern sector to an area of high pCO{sub 2} groundwaters. Reaction path modelling applied to this conceptual model, involving gas-water-rock interaction, highlights an intense degassing process in the aquifer controlling the chemical and isotopic composition of dissolved gases, total dissolved inorganic C (TDIC) and submarine gas emission. Mapping of TDIC shows a unique area of high values situated SSE of Vesuvio volcano with an average TDIC value of 0.039 mol/L, i.e., one order of magnitude higher than groundwaters from other sectors of the volcano. On the basis of TDIC values, the amount of CO{sub 2} transported by Vesuvio groundwaters was estimated at about 150 t/d. This estimate does not take into account the fraction of gas loss by degassing, however, it represents a relevant part of the CO{sub 2} emitted in this quiescent period by the Vesuvio volcanic system, being of the same order of magnitude as the CO{sub 2} diffusely degassed from the crater area.

Volcanic degassing at Somma-Vesuvio (Italy) inferred by chemical and isotopic signatures of groundwater

International Nuclear Information System (INIS)

Caliro, S.; Chiodini, G.; Avino, R.; Cardellini, C.; Frondini, F.

2005-01-01

A geochemical model is proposed for water evolution at Somma-Vesuvio, based on the chemical and isotopic composition of groundwaters, submarine gas emission and chemical composition of the dissolved gases. The active degassing processes, present in the highest part of the volcano edifice, strongly influence the groundwater evolution. The geological-volcanological setting of the volcano forces the waters infiltrating at Somma-Vesuvio caldera, enriched in volcanic gases, to flow towards the southern sector to an area of high pCO 2 groundwaters. Reaction path modelling applied to this conceptual model, involving gas-water-rock interaction, highlights an intense degassing process in the aquifer controlling the chemical and isotopic composition of dissolved gases, total dissolved inorganic C (TDIC) and submarine gas emission. Mapping of TDIC shows a unique area of high values situated SSE of Vesuvio volcano with an average TDIC value of 0.039 mol/L, i.e., one order of magnitude higher than groundwaters from other sectors of the volcano. On the basis of TDIC values, the amount of CO 2 transported by Vesuvio groundwaters was estimated at about 150 t/d. This estimate does not take into account the fraction of gas loss by degassing, however, it represents a relevant part of the CO 2 emitted in this quiescent period by the Vesuvio volcanic system, being of the same order of magnitude as the CO 2 diffusely degassed from the crater area

High cesium concentrations in groundwater in the upper 1.2 km of fractured crystalline rock - Influence of groundwater origin and secondary minerals

Science.gov (United States)

Mathurin, Frédéric A.; Drake, Henrik; Tullborg, Eva-Lena; Berger, Tobias; Peltola, Pasi; Kalinowski, Birgitta E.; Åström, Mats E.

2014-05-01

Dissolved and solid phase cesium (Cs) was studied in the upper 1.2 km of a coastal granitoid fracture network on the Baltic Shield (Äspö Hard Rock Laboratory and Laxemar area, SE Sweden). There unusually high Cs concentrations (up to 5-6 μg L-1) occur in the low-temperature (single and primary control of dissolved Cs in these systems. The high Cs concentrations in the saline groundwater is ascribed to long-term weathering of minerals, primarily Cs-enriched fracture coatings dominated by illite and mixed-layer clays and possibly wall rock micaceous minerals. The high Cs concentrations in the groundwater of marine origin are, in contrast, explained by relatively fast cation exchange reactions. As indicated by the field data and predicted by 1D solute transport modeling, alkali cations with low-energy hydration carried by intruding marine water are capable of (NH4+ in particular and K+ to some extent) replacing Cs+ on frayed edge (FES) sites on illite in the fracture coatings. The result is a rapid and persistent (at least in the order of decades) buildup of dissolved Cs concentrations in fractures where marine water flows downward. The identification of high Cs concentrations in young groundwater of marine origin and the predicted capacity of NH4+ to displace Cs from fracture solids are of particular relevance in the disposal of radioactive nuclear waste deep underground in crystalline rock.

Sea-water/groundwater interactions along a small catchment of the European Atlantic coast

International Nuclear Information System (INIS)

Einsiedl, Florian

2012-01-01

The geochemistry and isotopic composition of a karstic coastal aquifer in western Ireland has shed light on the effect of sea-water/groundwater interactions on the water quality of Ireland’s Atlantic coastal zone. The use of stable isotope data from the IAEA precipitation station in Valentia, located in SW Ireland has facilitated the characterization of groundwater recharge conditions in the western part of Ireland and suggests that groundwater is mostly replenished by the isotopically light winter precipitation. The dissolved SO 4 2- in the karstic groundwater that was collected during baseflow conditions with δ 34 S values between 4.6‰ and 18‰ may be composed of S stemming from three principal sources: SO 4 2- derived from precipitation which is composed of both sea-spray S (δ 34 S: 20‰) and an isotopically light anthropogenic source (δ 34 S: 1–5‰), SO 4 2- stemming from animal slurries (δ 34 S: ∼5‰), and intruding sea-water SO 4 2- (δ 34 S: 20.2‰). The isotopic composition of δ 18 O in dissolved groundwater SO 4 2- collected during baseflow conditions is interpreted as reflecting sea-water intrusion to the karstic coastal groundwater system. The highest δ 18 O values in dissolved groundwater SO 4 2- were in samples collected near the coast (4.8 ± 0.4‰) and the lowest (2 ± 0.5‰) were collected further inland. The δ 15 N and δ 18 O values of groundwater NO 3 - were between 3.4‰ and 11.4‰ and approximately 7.7‰, respectively, and reflect geochemical conditions in the aquifer that do not promote attenuation of NO 3 - through denitrification. As a result N loading to Kinvara Bay that is controlled by submarine groundwater discharge (SGD) was calculated as 5 tons/day on average compared to an estimated N-input that derives from precipitation of approximately 2.5 tons/a. SGD into the bay may result in near coastal sea-water quality changes. These results represent one of the first studies addressing the effect of groundwater

Groundwater-Quality Data in the South Coast Range-Coastal Study Unit, 2008: Results from the California GAMA Program

Science.gov (United States)

Mathany, Timothy M.; Burton, Carmen A.; Land, Michael; Belitz, Kenneth

2010-01-01

the 70 wells sampled, 3 surface-water samples were collected in streams near 2 of the sampled wells in order to better comprehend the interaction between groundwater and surface water in the area. The groundwater samples were analyzed for organic constituents (volatile organic compounds [VOC], pesticides and pesticide degradates, polar pesticides and metabolites, and pharmaceutical compounds), constituents of special interest (perchlorate, N-nitrosodimethylamine [NDMA], and 1,2,3-TCP), naturally occurring inorganic constituents (trace elements, nutrients, dissolved organic carbon [DOC], major and minor ions, silica, total dissolved solids [TDS], and alkalinity), and radioactive constituents (gross alpha and gross beta radioactivity). Naturally occurring isotopes (stable isotopes of hydrogen and oxygen in water, stable isotopes of nitrogen and oxygen in dissolved nitrate, stable isotopes of sulfur in dissolved sulfate, stable isotopes of carbon in dissolved inorganic carbon, activities of tritium, and carbon-14 abundance), and dissolved gases (including noble gases) also were measured to help identify the sources and ages of the sampled groundwater. In total, 298 constituents and field water-quality indicators were investigated. Three types of quality-control samples (blanks, replicates, and matrix-spikes) were collected at approximately 3 to 12 percent of the wells in the SCRC study unit, and the results for these samples were used to evaluate the quality of the data for the groundwater samples. Field blanks rarely contained detectable concentrations of any constituent, suggesting that contamination from sample collection procedures was not a significant source of bias in the data for the groundwater samples. Differences between replicate samples generally were less than 10 percent relative and/or standard deviation, indicating acceptable analytical reproducibility. Matrix-spike recoveries were within the acceptable range (70 to 130 percent) for approximately 84

Evaluation of the sustainability of deep groundwater as an arsenic-safe resource in the Bengal Basin

OpenAIRE

Michael, Holly A.; Voss, Clifford I.

2008-01-01

Tens of millions of people in the Bengal Basin region of Bangladesh and India drink groundwater containing unsafe concentrations of arsenic. This high-arsenic groundwater is produced from shallow (150 m where groundwater arsenic concentrations are nearly uniformly low, and many more wells are needed, however, the sustainability of deep, arsenic-safe groundwater has not been previously assessed. Deeper pumping could induce downward migration of dissolved arsenic, permanently destroying the dee...

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

Seawater-groundwater exchange and nutrients carried by submarine groundwater discharge in different types of wetlands at Jiaozhou Bay, China

Science.gov (United States)

Qu, Wenjing; Li, Hailong; Huang, Hao; Zheng, Chunmiao; Wang, Chaoyue; Wang, Xuejing; Zhang, Yan

2017-12-01

In Jiaozhou Bay, there are four wetland types, including sandy beaches, mud flats, tidal marshes, and estuarine intertidal zones. Four typical transects representing each of the wetland types were selected to investigate the flow dynamics, seawater-groundwater exchange and nutrients carried by submarine groundwater discharge (SGD). Based on field measurements of groundwater heads and salinity along each transect, the SGD averaged over the observation period was estimated using generalized Darcy's law. The SGD along the four transects ranges from 3.6 × 10-3 to 7.6 cm/d with the maximum occurring at the sandy beach. The SGD rate has a good correlation with the hydraulic conductivities of the wetland sediments. There is a positive correlation between the ratio of NO3-N/DIN and SGD rates. The SGD-associated nutrient output rate ranges from 3.3 × 10-2 to 9.5 mmol/m2/d for DIN (dissolved inorganic nitrogen), and from 6.2 × 10-5 to 1.8 × 10-2 mmol/m2/d for DIP (dissolved inorganic phosphorus). Compared to the nutrients delivered by the river, nutrients carried by SGD provide a more important source for the phosphate-limited environment to plankton in Jiaozhou Bay.

QA issues for site hydrochemical data used for groundwater evolution models

Energy Technology Data Exchange (ETDEWEB)

Savage, D. [Quintessa Ltd., Nottingham (United Kingdom); Miller, B. [QuantiSci Ltd., Melton Mowbray (United Kingdom); Sasamoto, Hiroshi; Yui, Mikazu [Japan Nuclear Cycle Development Inst., Tokai Works, Tokai, Ibaraki (Japan)

1999-06-01

Groundwater data used for modelling site or repository evolution need to be assessed for their quality and whether they are 'fit for purpose', prior to utilization. This report discuss factors and issues which impinge upon the quality of such data. It is recommended that geochemical modelleres: are aware of how groundwater samples were collected, whether during drilling, during hydraulic testing, or thereafter, by in-situ measurement, pumped from boreholes, or by pressurised sampler; are aware of what procedures (if any) were used to 'correct' samples for drill fluid contamination and what errors were associated with those methods; are aware of whether samples were subject to de-pressurisation during sampling, and whether geochemical modelling techniques were applied to correct the compositions of samples for that process; request different measures of redox activity (e.g., electrode measurements of Eh, concentrations of different redox-sensitive aqueous species) to be applied to key groundwater samples to investigate the extent of redox equilibrium; are aware of how groundwater samples were filtered and preserved for off-site analysis; ensure that adequate methods of groundwater filtration (< 0.1 {mu}m) and chemical analysis are applied to ensure accurate and reproducible analyses for dissolved aluminum at low levels of concentration (generally less than 0.2 mg/L); are aware of elemental errors and detection limits in chemical analysis of groundwater samples and assess the quality of groundwater analyses via ion exchange balances and via a comparison of measured and calculated values for total dissolved solids contents; ensure that detailed mineralogical analysis is carried out on rock samples from locations where key groundwater samples have been extracted. (author)

QA issues for site hydrochemical data used for groundwater evolution models

International Nuclear Information System (INIS)

Savage, D.; Miller, B.; Sasamoto, Hiroshi; Yui, Mikazu

1999-06-01

Groundwater data used for modelling site or repository evolution need to be assessed for their quality and whether they are 'fit for purpose', prior to utilization. This report discuss factors and issues which impinge upon the quality of such data. It is recommended that geochemical modelleres: are aware of how groundwater samples were collected, whether during drilling, during hydraulic testing, or thereafter, by in-situ measurement, pumped from boreholes, or by pressurised sampler; are aware of what procedures (if any) were used to 'correct' samples for drill fluid contamination and what errors were associated with those methods; are aware of whether samples were subject to de-pressurisation during sampling, and whether geochemical modelling techniques were applied to correct the compositions of samples for that process; request different measures of redox activity (e.g., electrode measurements of Eh, concentrations of different redox-sensitive aqueous species) to be applied to key groundwater samples to investigate the extent of redox equilibrium; are aware of how groundwater samples were filtered and preserved for off-site analysis; ensure that adequate methods of groundwater filtration (< 0.1 μm) and chemical analysis are applied to ensure accurate and reproducible analyses for dissolved aluminum at low levels of concentration (generally less than 0.2 mg/L); are aware of elemental errors and detection limits in chemical analysis of groundwater samples and assess the quality of groundwater analyses via ion exchange balances and via a comparison of measured and calculated values for total dissolved solids contents; ensure that detailed mineralogical analysis is carried out on rock samples from locations where key groundwater samples have been extracted. (author)

Baseline assessment of groundwater quality in Pike County, Pennsylvania, 2015

Science.gov (United States)

Senior, Lisa A.; Cravotta, Charles A.

2017-12-29

The Devonian-age Marcellus Shale and the Ordovician-age Utica Shale, which have the potential for natural gas development, underlie Pike County and neighboring counties in northeastern Pennsylvania. In 2015, the U.S. Geological Survey, in cooperation with the Pike County Conservation District, conducted a study that expanded on a previous more limited 2012 study to assess baseline shallow groundwater quality in bedrock aquifers in Pike County prior to possible extensive shale-gas development. Seventy-nine water wells ranging in depths from 80 to 610 feet were sampled during June through September 2015 to provide data on the presence of methane and other aspects of existing groundwater quality in the various bedrock geologic units throughout the county, including concentrations of inorganic constituents commonly present at low values in shallow, fresh groundwater but elevated in brines associated with fluids extracted from geologic formations during shale-gas development. All groundwater samples collected in 2015 were analyzed for bacteria, dissolved and total major ions, nutrients, selected dissolved and total inorganic trace constituents (including metals and other elements), radon-222, gross alpha- and gross beta-particle activity, dissolved gases (methane, ethane, and propane), and, if sufficient methane was present, the isotopic composition of methane. Additionally, samples from 20 wells distributed throughout the county were analyzed for selected man-made volatile organic compounds, and samples from 13 wells where waters had detectable gross alpha activity were analyzed for radium-226 on the basis of relatively elevated gross alpha-particle activity.Results of the 2015 study show that groundwater quality generally met most drinking-water standards for constituents and properties included in analyses, but groundwater samples from some wells had one or more constituents or properties, including arsenic, iron, manganese, pH, bacteria, sodium, chloride, sulfate

Bacterial sulphate reduction and mixing processes at the Aespoe Hard Rock Laboratory indicated by groundwater δ34S isotope signatures

International Nuclear Information System (INIS)

Wallin, Bill

2011-04-01

This report includes data mostly obtained from δ 34 S isotope measurements of groundwater at the Aespoe Island and one sampling from the Laxemar site, southeastern Sweden, during tunnel construction. Early sampling at Aespoe (up to 1992), before tunnel excavation, indicates a groundwater system with multiple sulphur sources. The isotope changes over time in the dissolved sulphate were studied during a sampling campaign in the monitoring phase from 1993 to 1995. A total of 88 samples were collected by SKB between 1992 and 1995 from core-drilled surface boreholes and from boreholes drilled in the tunnel (34 of these samples were collected from the tunnel boreholes). The results of the analyses have been the focus of discussion of the isotope changes with time in the dissolved sulphate (SO 4 2- ). The results indicate that the sulphur isotope signatures in the dissolved sulphate of the groundwater and those from fracture-filling sulphides at Aespoe originate from multiple sulphur sources in the groundwater at Aespoe and Laxemar. The data may be grouped as follows: a) typically homogeneous marine signatures of dissolved SO 4 2- are observed, with δ 34 S values of approximately +21 per mille CDT at intermediate depths of approximately 100-250 m; b) dissolved sulphate in the groundwater at greater depths (below 600 m) with average values of approximately +10 per mille CDT; and c) a dissolved SO 4 2- originating from a mixture of these sulphur sources (100-600m), although there is a difference between a mixture and modification by reduction. Reduced sulphur with low δ 34 S values is also recorded in fracture-filling sulphides, with δ 34 S values of approximately 0 to -10 per mille CDT. This may contribute to small changes in the isotope signature of the dissolved SO 4 2- , probably by sulphide oxidation in the past. The changes in the δ 34 S isotope data for dissolved SO 4 2- over the 1992-1996 period suggest a complex situation, indicating both sulphate reduction by

Continuous in-situ monitoring of dissolved gases for the characterization of the Critical Zone with a MIMS

Science.gov (United States)

Chatton, Eliot; Labasque, Thierry; Aquilina, Luc; de la Bernardie, Jérôme; Guihéneuf, Nicolas

2016-04-01

In the perspective of a temporal and spatial exploration of the Critical Zone, we developed an in situ monitoring instrument for continuous dissolved gas analysis (N2, O2, CO2, CH4, He, Ne, Ar, Kr, Xe). With a large resolution (5 orders of magnitude) and a capability of high frequency multi-tracer analysis (1 gas every 1.5 seconds), the MIMS (Membrane Inlet Mass Spectrometer) is an innovative tool allowing the investigation of a large panel of physical and biogeochemical processes. First of all, this study presents the results of groundwater tracer tests using dissolved gases in order to evaluate transport properties of a fractured media in Brittany, France (Ploemeur, ORE H+). The tracer test experiment showed that the MIMS is perfectly suitable for field work. The instrument provides precise measurements accurate enough to produce breakthrough curves during groundwater tracer tests. The results derived from 4He data gives transport parameters in good agreement with the results obtained with a fluorescent tracer. Combined with a pump and a multi-parameter probe, the MIMS is also capable to perform accurate dissolved gases well-logs allowing a real-time estimation of recharge conditions (temperature, excess air), aquifer stratification, redox conditions and groundwater residence time by 4He dating. Therefore, the MIMS is a valuable tool for in situ characterization of biogeochemical reactivity in aquatic systems, the determination of aquifer transport properties, the monitoring of groundwater recharge conditions and the characterization of aquifer-river exchanges.

Catchment tracers reveal discharge, recharge and sources of groundwater-borne pollutants in a novel lake modelling approach

Directory of Open Access Journals (Sweden)

E. Kristensen

2018-02-01

Full Text Available Groundwater-borne contaminants such as nutrients, dissolved organic carbon (DOC, coloured dissolved organic matter (CDOM and pesticides can have an impact the biological quality of lakes. The sources of pollutants can, however, be difficult to identify due to high heterogeneity in groundwater flow patterns. This study presents a novel approach for fast hydrological surveys of small groundwater-fed lakes using multiple groundwater-borne tracers. Water samples were collected from the lake and temporary groundwater wells, installed every 50 m within a distance of 5–45 m to the shore, were analysed for tracer concentrations of CDOM, DOC, total dissolved nitrogen (TDN, groundwater only, total nitrogen (TN, lake only, total dissolved phosphorus (TDP, groundwater only, total phosphorus (TP, lake only, δ18O ∕ δ16O isotope ratios and fluorescent dissolved organic matter (FDOM components derived from parallel factor analysis (PARAFAC. The isolation of groundwater recharge areas was based on δ18O measurements and areas with a high groundwater recharge rate were identified using a microbially influenced FDOM component. Groundwater discharge sites and the fractions of water delivered from the individual sites were isolated with the Community Assembly via Trait Selection model (CATS. The CATS model utilized tracer measurements of TDP, TDN, DOC and CDOM from the groundwater samples and related these to the tracer measurements of TN, TP, DOC and CDOM in the lake. A direct comparison between the lake and the inflowing groundwater was possible as degradation rates of the tracers in the lake were taken into account and related to a range of water retention times (WRTs of the lake (0.25–3.5 years in 0.25-year increments. These estimations showed that WRTs above 2 years required a higher tracer concentration of inflowing water than found in any of the groundwater wells around the lake. From the estimations of inflowing tracer concentration

Influence of groundwater composition on subsurface iron and arsenic removal

KAUST Repository

Moed, David H.; Van Halem, Doris; Verberk, J. Q J C; Amy, Gary L.; Van Dijk, Johannis C.

2012-01-01

Subsurface arsenic and iron removal (SAR/SIR) is a novel technology to remove arsenic, iron and other groundwater components by using the subsoil. This research project investigated the influence of the groundwater composition on subsurface treatment. In anoxic sand column experiments, with synthetic groundwater and virgin sand, it was found that several dissolved substances in groundwater compete for adsorption sites with arsenic and iron. The presence of 0.01 mmol L -1phosphate, 0.2 mmol L -1 silicate, and 1 mmol L -1 nitrate greatly reduced the efficiency of SAR, illustrating the vulnerability of this technology in diverse geochemical settings. SIR was not as sensitive to other inorganic groundwater compounds, though iron retardation was limited by 1.2 mmol L -1 calcium and 0.06 mmol L -1 manganese. © IWA Publishing 2012.

Influence of groundwater composition on subsurface iron and arsenic removal

KAUST Repository

Moed, David H.

2012-06-01

Subsurface arsenic and iron removal (SAR/SIR) is a novel technology to remove arsenic, iron and other groundwater components by using the subsoil. This research project investigated the influence of the groundwater composition on subsurface treatment. In anoxic sand column experiments, with synthetic groundwater and virgin sand, it was found that several dissolved substances in groundwater compete for adsorption sites with arsenic and iron. The presence of 0.01 mmol L -1phosphate, 0.2 mmol L -1 silicate, and 1 mmol L -1 nitrate greatly reduced the efficiency of SAR, illustrating the vulnerability of this technology in diverse geochemical settings. SIR was not as sensitive to other inorganic groundwater compounds, though iron retardation was limited by 1.2 mmol L -1 calcium and 0.06 mmol L -1 manganese. © IWA Publishing 2012.

Non-conservative behavior of fluorescent dissolved organic matter (FDOM) within a subterranean estuary

Science.gov (United States)

Suryaputra, I. G. N. A.; Santos, I. R.; Huettel, M.; Burnett, W. C.; Dittmar, T.

2015-11-01

The role of submarine groundwater discharge (SGD) in releasing fluorescent dissolved organic matter (FDOM) to the coastal ocean and the possibility of using FDOM as a proxy for dissolved organic carbon (DOC) was investigated in a subterranean estuary in the northeastern Gulf of Mexico (Turkey Point, Florida). FDOM was continuously monitored for three weeks in shallow beach groundwater and in the adjacent coastal ocean. Radon (222Rn) was used as a natural groundwater tracer. FDOM and DOC correlated in groundwater and seawater samples, implying that FDOM may be a proxy of DOC in waters influenced by SGD. A mixing model using salinity as a seawater tracer revealed FDOM production in the high salinity region of the subterranean estuary. This production was probably a result of infiltration and transformation of labile marine organic matter in the beach sediments. The non-conservative FDOM behavior in this subterranean estuary differs from most surface estuaries where FDOM typically behaves conservatively. At the study site, fresh and saline SGD delivered about 1800 mg d-1 of FDOM (quinine equivalents) to the coastal ocean per meter of shoreline. About 11% of this input was related to fresh SGD, while 89% were related to saline SGD resulting from FDOM production within the shallow aquifer. If these fluxes are representative of the Florida Gulf Coast, SGD-derived FDOM fluxes would be equivalent to at least 18% of the potential regional riverine FDOM inputs. To reduce uncertainties related to the scarcity of FDOM data, further investigations of river and groundwater FDOM inputs in Florida and elsewhere are necessary.

Anaerobic biodegradation of dissolved ethanol in a pilot-scale sand aquifer: Variability in plume (redox) biogeochemistry

Science.gov (United States)

McLeod, Heather C.; Roy, James W.; Slater, Gregory F.; Smith, James E.

2018-01-01

The use of ethanol in alternative fuels has led to contamination of groundwater with high concentrations of this easily biodegradable organic compound. Previous laboratory and field studies have shown vigorous biodegradation of ethanol plumes, with prevalence of reducing conditions and methanogenesis. The objective of this study was to further our understanding of the dynamic biogeochemistry processes, especially dissolved gas production, that may occur in developing and aging plume cores at sites with ethanol or other organic contamination of groundwater. The experiment performed involved highly-detailed spatial and temporal monitoring of ethanol biodegradation in a 2-dimensional (175 cm high × 525 cm long) sand aquifer tank for 330 days, with a vertical shift in plume position and increased nutrient inputs occurring at Day 100. Rapid onset of fermentation, denitrification, sulphate-reduction and iron(III)-reduction occurred following dissolved ethanol addition, with the eventual widespread development of methanogenesis. The detailed observations also demonstrate a redox zonation that supports the plume fringe concept, secondary reactions resulting from a changing/moving plume, and time lags for the various biodegradation processes. Additional highlights include: i) the highest dissolved H2 concentrations yet reported for groundwater, possibly linked to vigorous fermentation in the absence of common terminal electron-acceptors (i.e., dissolved oxygen, nitrate, and sulphate, and iron(III)-minerals) and methanogenesis; ii) evidence of phosphorus nutrient limitation, which stalled ethanol biodegradation and perhaps delayed the onset of methanogenesis; and iii) the occurrence of dissimilatory nitrate reduction to ammonium, which has not been reported for ethanol biodegradation to date.

Groundwater salinity in coastal aquifer of Karachi, Pakistan

International Nuclear Information System (INIS)

Mashiatullah, A.; Qureshi, R.M.; Ahmad, E.; Tasneem, M.A.; Sajjad, M.I.; Khan, H.A.

2002-01-01

Potable groundwater salinity has become a problem of great concern in the Karachi Metropolis, which is not only the most populous and biggest industrial base but also the largest coastal dwelling of Pakistan. Stable isotope techniques [O/sup 18/ content of Oxygen in the water molecular and C/sup 13/ content of the Total Dissolved Inorganic Carbon (TDIC)] have been used, in conjunction with physiochemical tools (temperature, dissolved oxygen, pH, redox electrical conductivity, salinity), to examine the quality of potable water and the source of salinity. Surface water samples (12 No.) were collected from polluted streams, namely: Layeri River, Malir River; Hub River/Hub Lake and the Indus River. Shallow groundwater samples (7 No. ) were collected from operating dug wells. Relatively deep groundwater samples (12 No.) were collected from operating dug wells, relatively deep groundwater samples (12 No.) were collected from pumping wells/tube-wells. Physicochemical analysis of water samples was completed in the field. In the laboratory, water samples were analyzed for O/sup 18/ content of oxygen in the water molecule and C/sup 13/ content of the TDIC, using specific gas extraction systems and a modified GD-150 gas source mass spectrometer. It is concluded from this preliminary investigation that the potable aquifer system in coastal Karachi hosts a mixture of precipitation (rainwater only) from hinterlands, trapped seawater in relatively deep aquifer system, as well as intruded seawater under natural infiltration conditions and/or induced recharge conditions (in shallow aquifers). (author)

Alternative designs for petroleum product storage tanks for groundwater protection.

Science.gov (United States)

Oke Adeleke, Samson

In developing countries, there are numerous occurrences of petroleum product spillage in groundwater. The current practice of burying storage tanks beneath the surface without adequate safety devices facilitates this phenomenon. Underground tanks rust and leak, and spilled petroleum products migrate downward. The movement of the oil in the soil depends on its viscosity and quantity, the permeability of the soil/rock, and the presence of fractures within the rock. The oil spreads laterally in the form of a thin pancake due to its lower specific gravity, and soluble components dissolve in water. The pollution plume of petroleum products and dissolved phases moves in the direction of groundwater flow in the aquifer within the pores of soil and sediments or along fractures in basement complex areas. Most communities reply heavily on groundwater for potable and industrial supplies. However, the sustainability of this resource is under threat in areas where there are filling stations as a result of significant groundwater contamination from petroleum product spillage. Drinking water becomes unpalatable when it contains petroleum products in low concentrations, and small quantities may contaminate large volumes of water. Considering the losses incurred from spillage, the cost of cleaning the aquifer, and the fact that total cleansing and attenuation is impossible, the need to prevent spillage and if it happens to prevent it from getting into the groundwater system is of paramount importance. This paper proposes alternative design procedures with a view to achieving these objectives.

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

Groundwater hydrochemistry evaluation in rural Botswana: A ...

African Journals Online (AJOL)

... of groundwater from domestic water supply boreholes across rural Botswana. Ionic concentrations of K+, Na+, Ca2+, Mg2+, F-, Cl-, SO4 2-, HCO3 -, Fe3+, Mn-, and N. Parameters such as pH, total dissolved solids (TDS), and electrical conductance (EC) were correlated and their levels compared to international standards.

Research and development of groundwater dating (Part 3). A proposal of determination method for diffusion coefficients of dissolved helium in rock and applicability of estimation of diffusion coefficients using anions

International Nuclear Information System (INIS)

Higashihara, Tomohiro; Nakata, Kotaro; Hasegawa, Takuma

2006-01-01

Dissolved helium in groundwater is one of the most suitable tracers for the groundwater dating. The diffusion coefficients in aquitard and aquifer were important to estimate an accumulation of the helium in groundwater. However, few papers have been reported about the diffusion of helium in rocks. In this study, effective diffusion coefficients of the helium in sandstones and mudstone were determined using a through-diffusion method. The effective diffusion coefficients of helium were in the range of 1.5 x 10 -10 to 1.1 x 10 -9 m 2 s -1 and larger than those of Br - ions. Geometrical factors for the diffusion of helium were also larger than those for the diffusion of Br - ions. This fact suggests that diffusion path of helium in the rocks is not more restricted than that of Br - ions. The diffusion coefficients of helium were also estimated using the diffusion coefficient of helium in bulk water and formation factors for diffusion of Br - ions. The estimated diffusion coefficients of helium were larger than the effective diffusion coefficients. It is clarified that the effective diffusion coefficients of helium are underestimated by the estimation method using anions. (author)

Impact of stormwater infiltration basins on groundwater quality, Perth metropolitan region, Western Australia

Science.gov (United States)

Appleyard, S. J.

1993-08-01

Twelve bores were sunk adjacent to three stormwater infiltration basins in the Perth metropolitan area to examine the impact of runoff from a light industrial area, a medium-density residential area, and a major arterial road on groundwater quality, and to examine the hydrological response of the aquifer to runoff recharge. Automatic and manual water level monitoring between April and November 1990 indicated that groundwater levels responded within minutes to recharge from the infiltration basins. Peak water levels of up to 2.5 m above rest levels occurred 6 24 h after the commencement of ponding in the infiltration basins. There was a marked reduction in salinity and increase in dissolved oxygen concentrations in the upper part of the aquifer downgradient of the infiltration basins. Concentrations of toxic metals, nutrients, pesticides, and phenolic compounds in groundwater near the infiltration basins were low and generally well within Australian drinking water guidelines. However, sediment in the base of an infiltration basin draining a major road contained in excess of 3500 ppm of lead. Phthalates, which are US EPA priority pollutants, were detected in all but one bore near the infiltration basins. Their detection may be a sampling artifact, but they may also be derived from the plastic litter that accumulates in the infiltration basins. The concentration of iron in groundwater near the infiltration basins appears to be controlled by dissolved oxygen concentrations, with high iron concentrations occurring where dissolved oxygen concentrations are low. Pumping bores located near infiltration basins may suffer from iron encrustation problems caused by the mixing of shallow, oxygenated groundwater with water containing higher concentrations of iron from deeper in the aquifer.

Chlorinated solvents in groundwater of the United States

Science.gov (United States)

Moran, M.J.; Zogorski, J.S.; Squillace, P.J.

2007-01-01

Four chlorinated solvents-methylene chloride, perchloroethene (PCE), 1,1,1-trichloroethane, and trichloroethene (TCE)-were analyzed in samples of groundwater taken throughout the conterminous United States by the U.S. Geological Survey. The samples were collected between 1985 and 2002 from more than 5,000 wells. Of 55 volatile organic compounds (VOCs) analyzed in groundwater samples, solvents were among the most frequently detected. Mixtures of solvents in groundwater were common and may be the result of common usage of solvents or degradation of one solvent to another. Relative to other VOCs with Maximum Contaminant Levels (MCLs), PCE and TCE ranked high in terms of the frequencies of concentrations greater than or near MCLs. The probability of occurrence of solvents in groundwater was associated with dissolved oxygen content of groundwater, sources such as urban land use and population density, and hydraulic properties of the aquifer. The results reinforce the importance of understanding the redox conditions of aquifers and the hydraulic properties of the saturated and vadose zones in determining the intrinsic susceptibility of groundwater to contamination by solvents. The results also reinforce the importance of controlling sources of solvents to groundwater. ?? 2007 American Chemical Society.

Overview of groundwater quality in the Piceance Basin, western Colorado, 1946--2009

Science.gov (United States)

Thomas, J.C.; McMahon, P.B.

2013-01-01

Groundwater-quality data from public and private sources for the period 1946 to 2009 were compiled and put into a common data repository for the Piceance Basin. The data repository is available on the web at http://rmgsc.cr.usgs.gov/cwqdr/Piceance/index.shtml. A subset of groundwater-quality data from the repository was compiled, reviewed, and checked for quality assurance for this report. The resulting dataset consists of the most recently collected sample from 1,545 wells, 1,007 (65 percent) of which were domestic wells. From those samples, the following constituents were selected for presentation in this report: dissolved oxygen, dissolved solids, pH, major ions (chloride, sulfate, fluoride), trace elements (arsenic, barium, iron, manganese, selenium), nitrate, benzene, toluene, ethylbenzene, xylene, methane, and the stable isotopic compositions of water and methane. Some portion of recharge to most of the wells for which data were available was derived from precipitation (most likely snowmelt), as indicated by δ2H [H2O] and δ18O[H2O] values that plot along the Global Meteoric Water Line and near the values for snow samples collected in the study area. Ninety-three percent of the samples were oxic, on the basis of concentrations of dissolved oxygen that were greater than or equal to 0.5 milligrams per liter. Concentration data were compared with primary and secondary drinking-water standards established by the U.S. Environmental Protection Agency. Constituents that exceeded the primary standards were arsenic (13 percent), selenium (9.2 percent), fluoride (8.4 percent), barium (4.1 percent), nitrate (1.6 percent), and benzene (0.6 percent). Concentrations of toluene, xylenes, and ethylbenzene did not exceed standards in any samples. Constituents that exceeded the secondary standard were dissolved solids (72 percent), sulfate (37 percent), manganese (21 percent), iron (16 percent), and chloride (10 percent). Drinking-water standards have not been established for

Geochemical characterization and evaluation of groundwater suitability for domestic and agricultural utility in semi-arid region of Basara, Telangana State, South India

Science.gov (United States)

Adimalla, Narsimha; Venkatayogi, Sudarshan

2018-03-01

Hydrogeochemical investigations were carried out in semi-arid region of Basara to estimate the quality of groundwater for its suitability for domestic and agricultural purposes. For this region 34 groundwater samples were collected in different locations and analyzed for various ions, viz., Na+, Ca2+, Mg2+, K+, Cl-, HCO3 -, SO4 2-, CO3 2-, HCO3 -, NO3 - and F- to assess the water chemistry with sodium absorption ratio, %Na, residual sodium carbonate, magnesium hazard. The nitrate and fluoride concentrations were above the maximum permissible limit, while calcium, sodium, potassium and chloride were found below the desirable limits in most of the groundwater samples. The Wilcox diagram illustrates that 59% of the samples belong to excellent to good category, while the US Salinity Laboratory diagram indicates medium salinity/low sodium content in 64.70% of samples. In general, the geochemistry of groundwater in Basara region is influenced by the water rock processes through percolation and dissolution of rock forming minerals, while calculated values of saturation index for Anhydrite, Aragonite, Artinite, Brucite, Calcite, Fluorite, Gypsum, Dolomite and Magnesite of the groundwater samples were less than zero, indicating under-saturation. Chadha rectangular diagram for geochemical classification and hydrochemical processes of groundwater for Basara provinces indicates 50% of Na+-Cl-, 29% of Ca2+-Mg2+-Cl- and 18% of the water samples concentrate in the category of Na+-HCO3 - type.

Modeling Effects of Groundwater Basin Closure, and Reversal of Closure, on Groundwater Quality

Science.gov (United States)

Pauloo, R.; Guo, Z.; Fogg, G. E.

2017-12-01

Population growth, the expansion of agriculture, and climate uncertainties have accelerated groundwater pumping and overdraft in aquifers worldwide. In many agricultural basins, a water budget may be stable or not in overdraft, yet disconnected ground and surface water bodies can contribute to the formation of a "closed" basin, where water principally exits the basin as evapotranspiration. Although decreasing water quality associated with increases in Total Dissolved Solids (TDS) have been documented in aquifers across the United States in the past half century, connections between water quality declines and significant changes in hydrologic budgets leading to closed basin formation remain poorly understood. Preliminary results from an analysis with a regional-scale mixing model of the Tulare Lake Basin in California indicate that groundwater salinization resulting from open to closed basin conversion can operate on a decades-to-century long time scale. The only way to reverse groundwater salinization caused by basin closure is to refill the basin and change the hydrologic budget sufficiently for natural groundwater discharge to resume. 3D flow and transport modeling, including the effects of heterogeneity based on a hydrostratigraphic facies model, is used to explore rates and time scales of groundwater salinization and its reversal under different water and land management scenarios. The modeling is also used to ascertain the extent to which local and regional heterogeneity need to be included in order to appropriately upscale the advection-dispersion equation in a basin scale groundwater quality management model. Results imply that persistent managed aquifer recharge may slow groundwater salinization, and complete reversal may be possible at sufficiently high water tables.

The isotopic, chemical and dissolved gas concentrations in groundwater near Beaufort West

International Nuclear Information System (INIS)

Vogel, J.C.; Talma, A.S.; Heaton, T.H.E.

1980-01-01

Groundwater was collected from fifteen boreholes over an area of 500 sq km to the north-east of Beafort West, Cape Province, South Africa. Six boreholes were sampled at different depths using a pump equipped with inflatable packers. Samples were analysed for their carbon-14, tritium, oxygen-18, carbon-13, helium, nitrogen, argon, oxygen and radon-222 contents, uranium-234/uranium-238 activity ratios, and major ion chemistry. The study was a reconnaisance survey, but demonstrated the usefulness of multi-parameter investigations. The data are used in discussing the geohydrology of the area with emphasis on the recharge sources of groundwater in the pediment and at the foot of the surrounding escarpment

Assessment on seasonal variation of groundwater quality of phreatic aquifers - A river basin system

Digital Repository Service at National Institute of Oceanography (India)

Laluraj, C.M.; Gopinath, G.

suspended solids (TDS), fluoride and total iron content will help to identify the quality of ground water. Groundwater contamination can often have serious ill ef- fects on human health. Groundwater with low pH values can cause gastrointestinal disorders... is considered as an important parameter for irrigation and industrial purposes. Total dissolved solids help to identify the potability of groundwater. Total iron content may not have direct effects on human health but is of importance due to aesthetic reasons...

A pilot study for the extraction and treatment of groundwater from a manufactured gas plant site. Final report

International Nuclear Information System (INIS)

1997-12-01

This report describes a pilot study involving treatment of contaminated groundwater at a former manufactured gas plant site on the eastern seaboard of the US. The work was performed in order to provide the design basis for a full-scale groundwater extraction and treatment system at the site, as well as to develop a generic approach to selection of groundwater treatment sequences at other MGP sites. It included three main components: hydrogeologic investigations, bench-scale treatability studies, and pilot-scale treatability studies. Technologies evaluated in bench-scale work included gravity settling, filtration, and dissolved air flotation (DAF) for primary treatment of nonaqueous phase materials; biological degradation, air stripping, and carbon adsorption for secondary treatment of dissolved organics; and carbon adsorption as tertiary treatment of remaining dissolved contaminants. Pilot-scale studies focused on collecting system performance data fore three distinct levels of contamination. Two treatment trains were evaluated. One consisted of DAF, fluidized-bed biotreatment, and filtration plus carbon adsorption; the other used the same steps except to substitute air stripping for fluidized bed treatment. The final effluents produced by both treatment sequences were similar and demonstrated complete treatment of the groundwater. Besides detailing system design and performance for the treatability studies, the report includes an analysis of groundwater treatment applications to MGP sites in general, including a discussion of capital and operating costs

Fluvial fluxes of natural radium isotopes and dissolved barium for Ubatuba embayments, Sao Paulo

International Nuclear Information System (INIS)

Sousa, Keila Cristina Pinheiro Marchini de

2008-01-01

Radium isotopes are among the most important isotopes in the environment from both radioprotection and geo-hydrological points of view. They are also a powerful tool for studying geohydrological processes and have been used intensively as tracers of groundwater sources that discharge into the coastal ocean.The complex exchange of fluvial, subsurface and seawater within a coastal area directly affects global biogeochemical cycles. Environmental scientists have few tools to accurately quantify such processes and must therefore rely on various tracer techniques. Radium isotopes have been frequently applied as tracers of submarine groundwater discharge (SGD). The unique radium signature of SGD is acquired within the subterranean estuary, a mixing zone between fresh groundwater and seawater in coastal aquifers. In this study we determined the fluvial fluxes of the radium isotopes and dissolved barium for Ubatuba embayments, northernmost part of Sao Paulo Bight. The research work was carried out from April/ 2007 to August/ 2007 and covered 17 small rivers sources that belong to the major surface draining system of such coastal area. During this period of investigation, groundwater samples were also collected from 10 sources available in this coastal region. Activity concentrations of 223 Ra in riverine waters discharging to Ubatuba and Caraguatatuba embayments varied from -1 to 335 mBq 1000L -1 (in Cocanha River), while 224 Ra concentrations ranged from 17 mBq 100L -1 to 7270 mBq 100L -1 . Activity concentrations up to 1424 mBq 100L -1 were observed for 226 Ra in riverine waters, while 228 Ra concentrations varied from 1412 mBq 100L -1 to 4058 mBq 100L -1 . Groundwater activity concentrations of 223 Ra varied from 1 mBq 100L -1 to 126 mBq 100L -1 , while 224 Ra ranged from 118 mBq 100L -1 to 3701 mBq 100L -1 . 223 Ra/ 224 Ra activity ratios up to 0.7x10 -1 and 0.2 were observed in riverine and groundwater, respectively. For 226 Ra groundwater activity concentrations

Transient changes in shallow groundwater chemistry during the MSU ZERT CO2 injection experiment

Science.gov (United States)

Apps, J.A.; Zheng, Lingyun; Spycher, N.; Birkholzer, J.T.; Kharaka, Y.; Thordsen, J.; Kakouros, E.; Trautz, R.

2011-01-01

Food-grade CO2 was injected into a shallow aquifer through a perforated pipe placed horizontally 1-2 m below the water table at the Montana State University Zero Emission Research and Technology (MSU-ZERT) field site at Bozeman, Montana. The possible impact of elevated CO2 levels on groundwater quality was investigated by analyzing 80 water samples taken before, during, and following CO2 injection. Field determinations and laboratory analyses showed rapid and systematic changes in pH, alkalinity, and conductance, as well as increases in the aqueous concentrations of trace element species. The geochemical data were first evaluated using principal component analysis (PCA) in order to identify correlations between aqueous species. The PCA findings were then used in formulating a geochemical model to simulate the processes likely to be responsible for the observed increases in the concentrations of dissolved constituents. Modeling was conducted taking into account aqueous and surface complexation, cation exchange, and mineral precipitation and dissolution. Reasonable matches between measured data and model results suggest that: (1) CO2 dissolution in the groundwater causes calcite to dissolve. (2) Observed increases in the concentration of dissolved trace metals result likely from Ca+2-driven ion exchange with clays (smectites) and sorption/desorption reactions likely involving Fe (hydr)oxides. (3) Bicarbonate from CO2 dissolution appears to compete for sorption with anionic species such as HAsO4-2, potentially increasing dissolved As levels in groundwater. ?? 2011 Published by Elsevier Ltd.

Iron behavior in the ozonation and filtration of groundwater

Energy Technology Data Exchange (ETDEWEB)

Sallanko, J.; Lakso, E.; Ropelinen, J. [University of Oulu, Oulu (Finland)

2006-08-15

In Finnish groundwater, the main substances that require treatment are iron and manganese. In addition to this, groundwaters are soft and acidic. Iron removal is usually relatively effective by oxidizing dissolved iron into an insoluble form, either by aeration or chemical oxidation and removing the formed precipitate by sand filtration. Sometimes, if the untreated water contains high amounts of organic matter, problems may arise for iron removal. In Finland, it is quite common that groundwater contains high levels of both iron and natural organic matter, mainly as humic substances. The groundwater of the Kukkala intake plant in Liminka has been found to be problematic, due to its high level of natural organic matter. This research studied the removal of iron from this water by means of oxidation with ozone and filtration. While the oxidation of iron by ozone was rapid, the precipitate particles formed were small, and thus could not be removed by sand and anthracite filtration, and the iron residue in the treated water was more than 2 mg L{sup -1}. And while the filtration was able to remove iron well without the feed of ozone, the iron residue in the treated water was only 0.30 mg L{sup -1}. In this case, iron was led to the filter in a bivalent dissolved form. So, the result of iron removal was the best when the sand/anthracite filter functioned largely as an adsorption filter.

Assessment of groundwater quality at the Nigerian Institute for ...

African Journals Online (AJOL)

This study was carried out to ascertain the suitability of the Nigerian Institute for Oceanography and Marine Research's groundwater resources for aquaculture purposes. The samples were subjected to physico-chemical analyses and the parameters analyzed are Iron, pH, Sulphide ion Total Ammonia, Dissolved Oxygen, ...

Hydrochemical assessment of groundwater used for irrigation in Rumphi and Karonga districts, Northern Malawi

Science.gov (United States)

Wanda, Elijah M. M.; Gulula, Lewis C.; Phiri, Ambrose

Irrigation water quality is an essential component of sustainable agriculture. Irrigation water quality concerns have often been neglected over concerns of quantity in most irrigation projects in Malawi. In this study, a hydrochemical assessment of groundwater was carried out to characterize, classify groundwater and evaluate its suitability for irrigation use in Karonga and Rumphi districts, Northern Malawi. Groundwater samples were collected during wet (January-April 2011) and dry (July-September 2011) seasons from 107 shallow wells and boreholes drilled for rural water supply using standard sampling procedures. The water samples were analysed for pH, major ions, total dissolved solids and electrical conductivity (EC), using standard methods. Multivariate chemometric (such as Kruskal Wallis test), hydrographical methods (i.e. Piper diagram) and PHREEQC geochemical modelling program were used to characterise the groundwater quality. Electrical conductivity, percentage sodium ion (% Na+), residual sodium carbonate (RSC), total dissolved solids (TDS), sodium adsorption ratio (SAR), Kelly’s ratio (KR) and permeability index (PI) were used to evaluate the suitability of water for irrigation. It was established that groundwater is neutral to alkaline and mostly freshwater (TDS management is suggested for sustainable development of the water resources for better plant growth, long-term as well as maintaining human health in the study area.

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

Groundwater quality and hydrogeological characteristics of Malacca state in Malaysia

Directory of Open Access Journals (Sweden)

Shirazi Sharif Moniruzzaman

2015-03-01

Full Text Available Groundwater quality and aquifer productivity of Malacca catchment in Peninsular Malaysia are presented in this article. Pumping test data were collected from 210 shallow and 17 deep boreholes to get well inventory information. Data analysis confirmed that the aquifers consisting of schist, sand, limestone and volcanic rocks were the most productive aquifers for groundwater in Malacca state. GIS-based aquifer productivity map was generated based on bedrock and discharge capacity of the aquifers. Aquifer productivity map is classified into three classes, namely high, moderate and low based on discharge capacity. Groundwater potential of the study area is 35, 57 and 8% of low, moderate and high class respectively. Fifty two shallow and 14 deep aquifer groundwater samples were analyzed for water quality. In some cases, groundwater quality analysis indicated that the turbidity, total dissolved solids, iron, chloride and cadmium concentrations exceeded the limit of drinking water quality standards.

Hydrogeochemical investigations of groundwater in Ziarat valley, Baluchistan

International Nuclear Information System (INIS)

Akram, W.; Ahmad, M.; Rafiq, M.

2010-03-01

Present study was undertaken in Ziarat Valley, Baluchistan to investigate recent trends of groundwater chemistry (geochemical facies, geochemical evolution) and assess the groundwater quality for drinking and irrigation purposes. For this purpose samples of groundwater (open wells, tube wells, karezes, springs) were periodically collected from different locations and analyzed for dissolved chemical constituents such as sodium, potassium, magnesium, calcium, carbonate, bicarbonate, chloride and sulphate. The data indicated that concentrations of sodium, potassium, calcium and magnesium vary from 5 to 113,0.3 to 3,18 to 62 and 27 to 85 mg/l respectively. Values of anions i. e. bicarbonate, chloride and sulphate lie in the range of 184 to 418, 14 to 77 and 8 to 318 mg/l respectively. Hydrogeochemical facies revealed that groundwater in the study area belongs to Mg-HCO/sub 3/ type at 72% surveyed locations. Dissolution and calcite precipitation were found to be the main processes controlling the groundwater chemistry. Chemical quality was assessed for drinking use by comparing with WHO, Indian and proposed national standards, and for irrigation use using empirical indices such as SAR and RSC. The results show that groundwater is quite suitable for irrigation and drinking purposes. (author)

Evaluating hydrochemical data from shallow groundwater in Forsmark from a microbiological perspective

International Nuclear Information System (INIS)

Hallbeck, Lotta

2008-03-01

Oxygen is one of the chemical species that can corrode a copper canister in a KBS-3 repository. It is therefore important to determine whether oxygen dissolved in precipitation or groundwater could reach repository depth by groundwater transport. This matter can be determined by gaining an understanding of the oxygen-consuming microbial processes that take place in shallow groundwater in the area of interest. This report evaluates hydrogeochemical data from shallow groundwater in the Forsmark area from a microbiological perspective. Hydrogeochemical data were gathered from soil pipes at depths from 1.6 to 9.6 m and from percussion-drilled boreholes having mid-point depths of between c. 30 and c. 180 m. Only a few of the percussion-drilled boreholes had packers installed. The sampled sections were therefore very long, allowing groundwater from many different depths to mix. Oxygen and oxidation-reduction potential (ORP) were measured in groundwater in soil pipes but not in percussion-drilled boreholes. The poor quality of the oxygen data made it difficult to identify the depth of origin of completely oxygen-free groundwater. Parameters that indicated ongoing anaerobic microbial processes, such as nitrite, ferrous iron, dissolved manganese, and sulphide, were found in many soil pipes. The soil pipes displayed individual chemical profiles in terms of chemical species related to microbial activity. The microbial activity could not be linked to the classes of soil pipe, i.e. recharge, discharge, or intermittent. Existing soil pipes and percussion-drilled boreholes could be used for additional sampling of microbial parameters. Such sampling would benefit from careful hypothesis-driven description of the sampling parameters and experience-guided choice of sampling methods

Evaluating hydrochemical data from shallow groundwater in Forsmark from a microbiological perspective

Energy Technology Data Exchange (ETDEWEB)

Hallbeck, Lotta (Microbial Analytics Sweden AB, Goeteborg (Sweden))

2008-03-15

Oxygen is one of the chemical species that can corrode a copper canister in a KBS-3 repository. It is therefore important to determine whether oxygen dissolved in precipitation or groundwater could reach repository depth by groundwater transport. This matter can be determined by gaining an understanding of the oxygen-consuming microbial processes that take place in shallow groundwater in the area of interest. This report evaluates hydrogeochemical data from shallow groundwater in the Forsmark area from a microbiological perspective. Hydrogeochemical data were gathered from soil pipes at depths from 1.6 to 9.6 m and from percussion-drilled boreholes having mid-point depths of between c. 30 and c. 180 m. Only a few of the percussion-drilled boreholes had packers installed. The sampled sections were therefore very long, allowing groundwater from many different depths to mix. Oxygen and oxidation-reduction potential (ORP) were measured in groundwater in soil pipes but not in percussion-drilled boreholes. The poor quality of the oxygen data made it difficult to identify the depth of origin of completely oxygen-free groundwater. Parameters that indicated ongoing anaerobic microbial processes, such as nitrite, ferrous iron, dissolved manganese, and sulphide, were found in many soil pipes. The soil pipes displayed individual chemical profiles in terms of chemical species related to microbial activity. The microbial activity could not be linked to the classes of soil pipe, i.e. recharge, discharge, or intermittent. Existing soil pipes and percussion-drilled boreholes could be used for additional sampling of microbial parameters. Such sampling would benefit from careful hypothesis-driven description of the sampling parameters and experience-guided choice of sampling methods

Predicting redox conditions in groundwater at a regional scale

Science.gov (United States)

Tesoriero, Anthony J.; Terziotti, Silvia; Abrams, Daniel B.

2015-01-01

Defining the oxic-suboxic interface is often critical for determining pathways for nitrate transport in groundwater and to streams at the local scale. Defining this interface on a regional scale is complicated by the spatial variability of reaction rates. The probability of oxic groundwater in the Chesapeake Bay watershed was predicted by relating dissolved O2 concentrations in groundwater samples to indicators of residence time and/or electron donor availability using logistic regression. Variables that describe surficial geology, position in the flow system, and soil drainage were important predictors of oxic water. The probability of encountering oxic groundwater at a 30 m depth and the depth to the bottom of the oxic layer were predicted for the Chesapeake Bay watershed. The influence of depth to the bottom of the oxic layer on stream nitrate concentrations and time lags (i.e., time period between land application of nitrogen and its effect on streams) are illustrated using model simulations for hypothetical basins. Regional maps of the probability of oxic groundwater should prove useful as indicators of groundwater susceptibility and stream susceptibility to contaminant sources derived from groundwater.

The distribution of methane in groundwater in Alberta (Canada) and associated aqueous geochemistry conditions

Science.gov (United States)

Humez, Pauline; Mayer, Bernhard; Nightingale, Michael; Becker, Veith; Kingston, Andrew; Taylor, Stephen; Millot, Romain; Kloppmann, Wolfram

2016-04-01

Development of unconventional energy resources such as shale gas and coalbed methane has generated some public concern with regard to the protection of groundwater and surface water resources from leakage of stray gas from the deep subsurface. In terms of environmental impact to and risk assessment of shallow groundwater resources, the ultimate challenge is to distinguish: (a) natural in-situ production of biogenic methane, (b) biogenic or thermogenic methane migration into shallow aquifers due to natural causes, and (c) thermogenic methane migration from deep sources due to human activities associated with the exploitation of conventional or unconventional oil and gas resources. We have conducted a NSERC-ANR co-funded baseline study investigating the occurrence of methane in shallow groundwater of Alberta (Canada), a province with a long record of conventional and unconventional hydrocarbon exploration. Our objective was to assess the occurrence and sources of methane in shallow groundwaters and to also characterize the hydrochemical environment in which the methane was formed or transformed through redox processes. Ultimately our aim was to determine whether methane was formed in-situ or whether it migrated from deeper formations into shallow aquifers. Combining hydrochemical and dissolved and free geochemical gas data from 372 groundwater samples obtained from 186 monitoring wells of the provincial groundwater observation well network (GOWN) in Alberta, it was found that methane is ubiquitous in groundwater in Alberta and is predominantly of biogenic origin. The highest concentrations of dissolved biogenic methane (> 0.01 mM or > 0.2 mg/L), characterized by δ13CCH4 values deep thermogenic gas that had migrated in significant amounts into shallow aquifers either naturally or via anthropogenically induced pathways. This study shows that the combined interpretation of aqueous geochemistry data in concert with the chemical and isotopic composition of dissolved and

Major ions composition of the groundwater and surface water ...

African Journals Online (AJOL)

The total ionic concentration increases dramatically from the highlands towards the rift valley following the regional groundwater flow directions to low-lying regions characterized by low annual rainfall and high evapotranspiration. In the rift the total dissolved solids (TDS) variation is dramatic (in places more than 50 fold).

Groundwater Quality in Jingyuan County, a Semi-Humid Area in Northwest China

Directory of Open Access Journals (Sweden)

Wu Jianhua

2011-01-01

Full Text Available Groundwater quality assessment is an essential study which plays an important role in the rational development and utilization of groundwater in any part of the world. In the study, groundwater qualities in Jingyuan County, in Ningxia, China were assessed with entropy weighted water quality index method. In the assessment, 12 hydrochemical parameters including chloride, sulphate, sodium, iron, pH, total dissolved solid (TDS, total hardness (TH, nitrate, ammonia, nitrogen, fluoride, iodine and nitrite were selected. The assessment results show that the concentrations of iodine, TH, iron and TDS are the most influencing parameters affecting the groundwater quality. The assessment results are rational and are in consistency with the results of filed investigation of which both indicates the groundwater in Jingyuan County is fit for drinking.

Iron oxidation kinetics and phosphate immobilization along the flow-path from groundwater into surface water

Science.gov (United States)

van der Grift, B.; Rozemeijer, J. C.; Griffioen, J.; van der Velde, Y.

2014-11-01

The retention of phosphorus in surface waters through co-precipitation of phosphate with Fe-oxyhydroxides during exfiltration of anaerobic Fe(II) rich groundwater is not well understood. We developed an experimental field set-up to study Fe(II) oxidation and P immobilization along the flow-path from groundwater into surface water in an agricultural experimental catchment of a small lowland river. We physically separated tube drain effluent from groundwater discharge before it entered a ditch in an agricultural field. Through continuous discharge measurements and weekly water quality sampling of groundwater, tube drain water, exfiltrated groundwater, and surface water, we investigated Fe(II) oxidation kinetics and P immobilization processes. The oxidation rate inferred from our field measurements closely agreed with the general rate law for abiotic oxidation of Fe(II) by O2. Seasonal changes in climatic conditions affected the Fe(II) oxidation process. Lower pH and lower temperatures in winter (compared to summer) resulted in low Fe oxidation rates. After exfiltration to the surface water, it took a couple of days to more than a week before complete oxidation of Fe(II) is reached. In summer time, Fe oxidation rates were much higher. The Fe concentrations in the exfiltrated groundwater were low, indicating that dissolved Fe(II) is completely oxidized prior to inflow into a ditch. While the Fe oxidation rates reduce drastically from summer to winter, P concentrations remained high in the groundwater and an order of magnitude lower in the surface water throughout the year. This study shows very fast immobilization of dissolved P during the initial stage of the Fe(II) oxidation process which results in P-depleted water before Fe(II) is completely depleted. This cannot be explained by surface complexation of phosphate to freshly formed Fe-oxyhydroxides but indicates the formation of Fe(III)-phosphate precipitates. The formation of Fe(III)-phosphates at redox gradients

Knowledge and understanding of dissolved solids in the Rio Grande–San Acacia, New Mexico, to Fort Quitman, Texas, and plan for future studies and monitoring

Science.gov (United States)

Moyer, Douglas; Anderholm, Scott K.; Hogan, James F.; Phillips, Fred M.; Hibbs, Barry J.; Witcher, James C.; Matherne, Anne Marie; Falk, Sarah E.

2013-01-01

the Rio Grande study area. The pattern in dissolved-solids concentrations along the Rio Grande is one of increasing concentration with increasing distance downstream from Elephant Butte and Caballo Reservoirs. The concentration of dissolved solids in the Rio Grande doubles (approximately 500 to 1,000 mg/L) from below Elephant Butte Reservoir to El Paso and increases by more than a factor of 5 (approximately 500 to 3,200 mg/L) from below Elephant Butte Reservoir to Fort Quitman. Marked increases in the concentration of dissolved solids commonly coincide with contributions from agricultural drains, wastewater-treatment plants, regional groundwater, and upward-flowing saline groundwater. The greatest factor, from the surface-water system, in controlling dissolved solids in the Rio Grande is the amount of water that is being transported or stored. Annual variation in streamflow is influenced primarily by climate (precipitation and evaporation) and management of Elephant Butte and Caballo Reservoirs (water storage and release cycles). Seasonal variation in streamflow within the Rio Grande study area is generally categorized generally as irrigation (March–September) and nonirrigation (October–February) seasons; with streamflow in the Rio Grande is highest during the irrigation season and lowest during the nonirrigation season. Dissolved-solids loads during the irrigation season decrease between Leasburg and Fort Quitman primarily because of irrigation diversions and losses to the underlying alluvial aquifer. Conversely, dissolved-solids loads during the nonirrigation season increase between Caballo Dam and Fort Quitman primarily because of the inflow of dissolved solids from agricultural drains, wastewater-treatment plants, and groundwater with elevated concentrations of dissolved solids. Many studies have mass-balance budgets that account for the mass of dissolved solids transported along the Rio Grande. Results from mass-balance budgets developed for dissolved solids

Trends in concentrations of nitrate and total dissolved solids in public supply wells of the Bunker Hill, Lytle, Rialto, and Colton groundwater subbasins, San Bernardino County, California: Influence of legacy land use

Science.gov (United States)

Kent, Robert; Landon, Matthew K.

2013-01-01

Concentrations and temporal changes in concentrations of nitrate and total dissolved solids (TDS) in groundwater of the Bunker Hill, Lytle, Rialto, and Colton groundwater subbasins of the Upper Santa Ana Valley Groundwater Basin were evaluated to identify trends and factors that may be affecting trends. One hundred, thirty-one public-supply wells were selected for analysis based on the availability of data spanning at least 11 years between the late 1980s and the 2000s. Forty-one of the 131 wells (31%) had a significant (p relations of nitrate trends to depth, lateral position, and VOCs imply that increasing nitrate concentrations are associated with nitrate loading from historical agricultural land use and that more recent urban land use is generally associated with lower nitrate concentrations and greater VOC occurrence. Increasing TDS trends were associated with relatively greater current nitrate concentrations and relatively greater amounts of urban land. Decreasing TDS trends were associated with relatively greater amounts of natural land use. Trends in TDS concentrations were not related to depth, lateral position, or VOC occurrence, reflecting more complex factors affecting TDS than nitrate in the study area.

Environmental impact of municipal dumpsite leachate on ground-water quality in Jawaharnagar, Rangareddy, Telangana, India

Science.gov (United States)

Soujanya Kamble, B.; Saxena, Praveen Raj

2017-10-01

The aim of the present work was to study the impact of dumpsite leachate on ground-water quality of Jawaharnagar village. Leachate and ground-water samples were investigated for various physico-chemical parameters viz., pH, total dissolved solids (TDS), total hardness (TH), calcium (Ca2+), magnesium (Mg2+), sodium (Na+), potassium (K+), chloride (Cl-), carbonates (CO3 2-), bicarbonates (HCO3 -), nitrates (NO3 -), and sulphates (SO4 2-) during dry and wet seasons in 2015 and were reported. The groundwater was hard to very hard in nature, and the concentrations of total dissolved solids, chlorides, and nitrates were found to be exceeding the permissible levels of WHO drinking water quality standards. Piper plots revealed that the dominant hydrochemical facies of the groundwater were of calcium chloride (CaCl2) type and alkaline earths (Ca2+ and Mg2+) exceed the alkali (Na+ and SO4 2-), while the strong acids (Cl- and SO4 2-) exceed the weak acids (CO3 2- and HCO3 -). According to USSL diagram, all the ground-water samples belong to high salinity and low-sodium type (C3S1). Overall, the ground-water samples collected around the dumpsite were found to be polluted and are unfit for human consumption but can be used for irrigation purpose with heavy drainage and irrigation patterns to control the salinity.

Impact of storm water on groundwater quality below retention/detention basins.

Science.gov (United States)

Zubair, Arif; Hussain, Asif; Farooq, Mohammed A; Abbasi, Haq Nawaz

2010-03-01

Groundwater from 33 monitoring of peripheral wells of Karachi, Pakistan were evaluated in terms of pre- and post-monsoon seasons to find out the impact of storm water infiltration, as storm water infiltration by retention basin receives urban runoff water from the nearby areas. This may increase the risk of groundwater contamination for heavy metals, where the soil is sandy and water table is shallow. Concentration of dissolved oxygen is significantly low in groundwater beneath detention basin during pre-monsoon season, which effected the concentration of zinc and iron. The models of trace metals shown in basin groundwater reflect the land use served by the basins, while it differed from background concentration as storm water releases high concentration of certain trace metals such as copper and cadmium. Recharge by storm water infiltration decreases the concentration and detection frequency of iron, lead, and zinc in background groundwater; however, the study does not point a considerable risk for groundwater contamination due to storm water infiltration.

Modeling groundwater flow and quality

Science.gov (United States)

Konikow, Leonard F.; Glynn, Pierre D.; Selinus, Olle

2013-01-01

In most areas, rocks in the subsurface are saturated with water at relatively shallow depths. The top of the saturated zone—the water table—typically occurs anywhere from just below land surface to hundreds of feet below the land surface. Groundwater generally fills all pore spaces below the water table and is part of a continuous dynamic flow system, in which the fluid is moving at velocities ranging from feet per millennia to feet per day (Fig. 33.1). While the water is in close contact with the surfaces of various minerals in the rock material, geochemical interactions between the water and the rock can affect the chemical quality of the water, including pH, dissolved solids composition, and trace-elements content. Thus, flowing groundwater is a major mechanism for the transport of chemicals from buried rocks to the accessible environment, as well as a major pathway from rocks to human exposure and consumption. Because the mineral composition of rocks is highly variable, as is the solubility of various minerals, the human-health effects of groundwater consumption will be highly variable.

Assessment of fluoride in groundwater and urine, and prevalence of fluorosis among school children in Haryana, India

Science.gov (United States)

Haritash, A. K.; Aggarwal, Ankur; Soni, Jigyasa; Sharma, Khyati; Sapra, Mohnish; Singh, Bhupinder

2018-05-01

Considering the health effects of fluoride, the present study was undertaken to assess the concentration of fluoride in groundwater, and urine of school children in Bass region of Haryana state. Fluoride in groundwater was observed to vary from 0.5 to 2.4 mg/l with an average concentration of 0.46 mg/l. On the other hand, F- in urine ranged from below the detection limit to 1.8 mg/l among girls and 0.17-1.2 mg/l among the boys. Higher average concentration of fluoride in urine (0.65 mg/l for boys and 0.34 mg/l for girls) may be ascribed to exposure to bioavailable fluoride through food, milk, tea, toothpaste, etc., in addition to intake through groundwater. Relatively more intake of water and food by the boys might be the reason for more cases of severe dental fluorosis (44%) among boys compared to girls (29% cases of moderate to severe dental fluorosis). The groundwater quality for drinking was compromised with respect to dissolved solids, hardness, magnesium ions, and dissolved iron. Hydro-geochemical investigation revealed that rock-water interaction, in terms of direct cation exchange, dominantly regulates groundwater chemistry, and groundwater is of Ca-Na-HCO3 type.

Hydrochemistry and groundwater system of the Zerka Ma'in-Zara thermal field, Jordan

Science.gov (United States)

Rimawi, Omar; Salameh, Elias

1988-03-01

A groundwater flow model through the different geological successions from the Upper Cretaceous through the Lower Cretaceous Sandstone and older units is presented in this paper. The model is supported by the hydrochemical evolution of water types from the recharge areas in the highlands to discharge sites of thermal water at the slopes overlooking the Dead Sea. The thermal water discharged in the Zerka Ma'in-Zara areas consists of three end members mixed in different ratios with a component of old (many thousands of years) thermal water undersaturated in carbonate minerals and containing hundreds of milligrams per liter of free CO 2. The release of CO 2 gas upon discharge renders the water oversaturated with respect to carbonate minerals which results in aragonite precipitation. The elevated temperature of the water in the reservoir (73-82°C) is attributed to the presence of a heat-storing layer topping the aquifer.

In Situ Bioreduction of Uranium (VI) to Submicromolar Levels and Reoxidation by Dissolved Oxygen

International Nuclear Information System (INIS)

Wu, Weimin; Carley, Jack M.; Luo, Jian; Ginder-Vogel, Matthew A.; Cardenas, Erick; Leigh, Mary Beth; Hwang, Chaichi; Kelly, Shelly D.; Ruan, Chuanmin; Wu, Liyou; Van Nostrand, Joy; Gentry, Terry J.; Lowe, Kenneth Alan; Mehlhorn, Tonia L.; Carroll, Sue L.; Luo, Wensui; Fields, Matthew Wayne; Gu, Baohua; Watson, David B.; Kemner, Kenneth M.; Marsh, Terence; Tiedje, James; Zhou, Jizhong; Fendorf, Scott; Kitanidis, Peter K.; Jardine, Philip M.; Criddle, Craig

2007-01-01

Groundwater within Area 3 of the U.S. Department of Energy (DOE) Environmental Remediation Sciences Program (ERSP) Field Research Center at Oak Ridge, TN (ORFRC) contains up to 135 (micro)M uranium as U(VI). Through a series of experiments at a pilot scale test facility, we explored the lower limits of groundwater U(VI) that can be achieved by in-situ biostimulation and the effects of dissolved oxygen on immobilized uranium. Weekly 2 day additions of ethanol over a 2-year period stimulated growth of denitrifying, Fe(III)-reducing, and sulfate-reducing bacteria, and immobilization of uranium as U(IV), with dissolved uranium concentrations decreasing to low levels. Following sulfite addition to remove dissolved oxygen, aqueous U(VI) concentrations fell below the U.S. Environmental Protection Agency maximum contaminant limit (MCL) for drinking water ( -1 or 0.126 (micro)M). Under anaerobic conditions, these low concentrations were stable, even in the absence of added ethanol. However, when sulfite additions stopped, and dissolved oxygen (4.0-5.5 mg L -1 ) entered the injection well, spatially variable changes in aqueous U(VI) occurred over a 60 day period, with concentrations increasing rapidly from <0.13 to 2.0 (micro)M at a multilevel sampling (MLS) well located close to the injection well, but changing little at an MLS well located further away. Resumption of ethanol addition restored reduction of Fe(III), sulfate, and U(VI) within 36 h. After 2 years of ethanol addition, X-ray absorption near-edge structure spectroscopy (XANES) analyses indicated that U(IV) comprised 60-80% of the total uranium in sediment samples. At the completion of the project (day 1260), U concentrations in MLS wells were less than 0.1 (micro)M. The microbial community at MLS wells with low U(VI) contained bacteria that are known to reduce uranium, including Desulfovibrio spp. and Geobacter spp., in both sediment and groundwater. The dominant Fe(III)-reducing species were Geothrix spp

Subsurface Transport Behavior of Micro-Nano Bubbles and Potential Applications for Groundwater Remediation

Directory of Open Access Journals (Sweden)

Hengzhen Li

2013-12-01

Full Text Available Micro-nano bubbles (MNBs are tiny bubbles with diameters on the order of micrometers and nanometers, showing great potential in environmental remediation. However, the application is only in the beginning stages and remains to be intensively studied. In order to explore the possible use of MNBs in groundwater contaminant removal, this study focuses on the transport of MNBs in porous media and dissolution processes. The bubble diameter distribution was obtained under different conditions by a laser particle analyzer. The permeability of MNB water through sand was compared with that of air-free water. Moreover, the mass transfer features of dissolved oxygen in water with MNBs were studied. The results show that the bubble diameter distribution is influenced by the surfactant concentration in the water. The existence of MNBs in pore water has no impact on the hydraulic conductivity of sand. Furthermore, the dissolved oxygen (DO in water is greatly increased by the MNBs, which will predictably improve the aerobic bioremediation of groundwater. The results are meaningful and instructive in the further study of MNB research and applications in groundwater bioremediation.

Shallow ground-water conditions, Tom Green County, Texas

Science.gov (United States)

Lee, J.N.

1986-01-01

Most of the water needs of Tom Green County, Texas, are supplied by ground water; however, the city of San Angelo is supplied by surface water. Groundwater withdrawals during 1980 (latest year for which data are available) in Tom Green County totaled about 15,300 acre-feet, all derived from shallow aquifers. Shallow aquifers in this report refer to the ground-water system generally less than 400 feet deep that contains water with less than a 10,000 milligrams per liter concentration of dissolved solids; aquifers comprising this system include: The Leona, Comanche Peak, Trinity, Blaine, San Angelo, Choza, Bullwagon, Vale, Standpipe, and Arroyo aquifers.

Characterization of DOM in landfill leachate polluted groundwater with electrospary LC-MS

DEFF Research Database (Denmark)

Persson, L.; Alsberg, T.; Odham, G.

2001-01-01

Dissolved organic matter in leachate polluted groundwater, downgradient a landfill, was analysed with electrospray mass spectrometry. The results indicate that the DOM change qualitatively in the gradient, becoming more uniform in functional groups and hydrofobicity. Those changes may affect...

Delineating fresh water and brackish water aquifers by GIS and groundwater quality data

International Nuclear Information System (INIS)

Yasin, M.; Latif, M.

2007-01-01

This study was conducted in the Mona project area, Bhalwal, district Sargodha to delineate fresh water and brackish water aquifers by GIS (Geographic Information System) and historic groundwater quality data of 138 deep tube wells installed in the study area. The groundwater quality zonations were made by overlapping maps of TDS (Total Dissolved Solids), SAR (Sodium Adsorption Ratio) and RSC (Residual Sodium Carbonate). Seven zones of groundwater quality consisting of good, marginal, hazardous and their combinations were identified. The results indicated redistribution of salts in the aquifer and rise in water table in some parts of the study area from 1965-1997. (author)

Pathways for arsenic from sediments to groundwater to streams: Biogeochemical processes in the Inner Coastal Plain, New Jersey, USA

Science.gov (United States)

Barringer, Julia L.; Mumford, Adam; Young, Lily Y.; Reilly, Pamela A.; Bonin, Jennifer L.; Rosman, Robert

2010-01-01

The Cretaceous and Tertiary sediments that underlie the Inner Coastal Plain of New Jersey contain the arsenic-rich mineral glauconite. Streambed sediments in two Inner Coastal Plain streams (Crosswicks and Raccoon Creeks) that traverse these glauconitic deposits are enriched in arsenic (15–25 mg/kg), and groundwater discharging to the streams contains elevated levels of arsenic (>80 μg/L at a site on Crosswicks Creek) with arsenite generally the dominant species. Low dissolved oxygen, low or undetectable levels of nitrate and sulfate, detectable sulfide concentrations, and high concentrations of iron and dissolved organic carbon (DOC) in the groundwater indicate that reducing environments are present beneath the streambeds and that microbial activity, fueled by the DOC, is involved in releasing arsenic and iron from the geologic materials. In groundwater with the highest arsenic concentrations at Crosswicks Creek, arsenic respiratory reductase gene (arrA) indicated the presence of arsenic-reducing microbes. From extracted DNA, 16s rRNA gene sequences indicate the microbial community may include arsenic-reducing bacteria that have not yet been described. Once in the stream, iron is oxidized and precipitates as hydroxide coatings on the sediments. Arsenite also is oxidized and co-precipitates with or is sorbed to the iron hydroxides. Consequently, dissolved arsenic concentrations are lower in streamwater than in the groundwater, but the arsenic contributed by groundwater becomes part of the arsenic load in the stream when sediments are suspended during high flow. A strong positive relation between concentrations of arsenic and DOC in the groundwater samples indicates that any process—natural or anthropogenic—that increases the organic carbon concentration in the groundwater could stimulate microbial activity and thus increase the amount of arsenic that is released from the geologic materials.

Sustainable in-well vapor stripping: A design, analytical model, and pilot study for groundwater remediation

Science.gov (United States)

Sutton, Patrick T.; Ginn, Timothy R.

2014-12-01

A sustainable in-well vapor stripping system is designed as a cost-effective alternative for remediation of shallow chlorinated solvent groundwater plumes. A solar-powered air compressor is used to inject air bubbles into a monitoring well to strip volatile organic compounds from a liquid to vapor phase while simultaneously inducing groundwater circulation around the well screen. An analytical model of the remediation process is developed to estimate contaminant mass flow and removal rates. The model was calibrated based on a one-day pilot study conducted in an existing monitoring well at a former dry cleaning site. According to the model, induced groundwater circulation at the study site increased the contaminant mass flow rate into the well by approximately two orders of magnitude relative to ambient conditions. Modeled estimates for 5 h of pulsed air injection per day at the pilot study site indicated that the average effluent concentrations of dissolved tetrachloroethylene and trichloroethylene can be reduced by over 90% relative to the ambient concentrations. The results indicate that the system could be used cost-effectively as either a single- or multi-well point technology to substantially reduce the mass of dissolved chlorinated solvents in groundwater.

In-situ study of migration and transformation of nitrogen in groundwater based on continuous observations at a contaminated desert site

Science.gov (United States)

Zuo, Rui; Jin, Shuhe; Chen, Minhua; Guan, Xin; Wang, Jinsheng; Zhai, Yuanzheng; Teng, Yanguo; Guo, Xueru

2018-04-01

The objective of this study was to explore the controlling factors on the migration and transformation of nitrogenous wastes in groundwater using long-term observations from a contaminated site on the southwestern edge of the Tengger Desert in northwestern China. Contamination was caused by wastewater discharge rich in ammonia. Two long-term groundwater monitoring wells (Wells 1# and 2#) were constructed, and 24 water samples were collected. Five key indicators were tested: ammonia, nitrate, nitrite, dissolved oxygen, and manganese. A numerical method was used to simulate the migration process and to determine the migration stage of the main pollutant plume in groundwater. The results showed that at Well 1# the nitrogenous waste migration process had essentially been completed, while at Well 2# ammonia levels were still rising and gradually transitioning to a stable stage. The differences for Well 1# and Well 2# were primarily caused by differences in groundwater flow. The change in ammonia concentration was mainly controlled by the migration of the pollution plume under nitrification in groundwater. The nitrification rate was likely affected by changes in dissolved oxygen and potentially manganese.

Comparison of physico-chemical parameters of groundwater from shallow aquifers near 2 thermal power plants in Punjab

International Nuclear Information System (INIS)

Gill, S.K.; Sahota, S.K.; Sahota, G.P.S.; Sahota, B.K.; Sahota, H.S.

1993-01-01

Physico-chemical parameters of groundwater from shallow aquifers near thermal power plants at Bathinda and Ropar have been measured. Increase in metallic content of water is noted in both the cases due to deposition of coal fly ash from the power plants on the soil. High values of calcium chloride, calcium carbonate and total dissolved solids are observed in Bathinda groundwater while Ropar groundwater is rich in ferric, fluoride and nitrate contents. (author). 8 refs., 1 fig., 1 tab

Tailings From Mining Activities, Impact on Groundwater, and Remediation

Directory of Open Access Journals (Sweden)

Khalid Al-Rawahy

2001-12-01

Full Text Available Effluent wastes from mining operations and beneficiation processes are comprized mostly of the following pollutants: total suspended solids (TTS, alkalinity or acidity (pH, settleable solids, iron in ferrous mining, and dissolved metals in nonferrous mining. Suspended solids consist of small particles of solid pollutants that resist separation by conventional means. A number of dissolved metals are considered toxic pollutants. The major metal pollutants present in ore mining and beneficiation waste waters include arsenic, cadmium, copper, lead, mercury, nickel, and zinc. Tailings ponds are used for both the disposal of solid waste and the treatment of waste-water streams. The supernatant decanted from these ponds contains suspended solids and, at times, process reagents introduced to the water during ore beneficiation. Leakage of material from tailings pond into groundwater is one possible source of water pollution in the mining industry. Percolation of waste-water from impoundment may occur if tailings ponds are not properly designed. This paper addresses potential groundwater pollution due to effluent from mining activities, and the possible remediation options.

Cl/Br ratios and chlorine isotope evidences for groundwater salinization and its impact on groundwater arsenic, fluoride and iodine enrichment in the Datong basin, China.

Science.gov (United States)

Li, Junxia; Wang, Yanxin; Xie, Xianjun

2016-02-15

In order to identify the salinization processes and its impact on arsenic, fluoride and iodine enrichment in groundwater, hydrogeochemical and environmental isotope studies have been conducted on groundwater from the Datong basin, China. The total dissolved solid (TDS) concentrations in groundwater ranged from 451 to 8250 mg/L, and 41% of all samples were identified as moderately saline groundwater with TDS of 3000-10,000 mg/L. The results of groundwater Cl concentrations, Cl/Br molar ratio and Cl isotope composition suggest that three processes including water-rock interaction, surface saline soil flushing, and evapotranspiration result in the groundwater salinization in the study area. The relatively higher Cl/Br molar ratio in groundwater from multiple screening wells indicates the contribution of halite dissolution from saline soil flushed by vertical infiltration to the groundwater salinization. However, the results of groundwater Cl/Br molar ratio model indicate that the effect of saline soil flushing practice is limited to account for the observed salinity variation in groundwater. The plots of groundwater Cl vs. Cl/Br molar ratio, and Cl vs δ(37)Cl perform the dominant effects of evapotranspiration on groundwater salinization. Inverse geochemical modeling results show that evapotranspiration may cause approximately 66% loss of shallow groundwater to account for the observed hydrochemical pattern. Due to the redox condition fluctuation induced by irrigation activities and evapotranspiration, groundwater salinization processes have negative effects on groundwater arsenic enrichment. For groundwater iodine and fluoride enrichment, evapotranspiration partly accounts for their elevation in slightly saline water. However, too strong evapotranspiration would restrict groundwater fluoride concentration due to the limitation of fluorite solubility. Copyright © 2015. Published by Elsevier B.V.

Impact of Coastal Development and Marsh Width Variability on Groundwater Quality in Estuarine Tidal Creeks

Science.gov (United States)

Shanahan, M.; Wilson, A. M.; Smith, E. M.

2017-12-01

Coastal upland development has been shown to negatively impact surface water quality in tidal creeks in the southeastern US, but less is known about its impact on groundwater. We sampled groundwater in the upland and along the marsh perimeter of tidal creeks located within developed and undeveloped watersheds. Samples were analyzed for salinity, dissolved organic carbon, nitrogen and phosphorus concentrations. Groundwater samples collected from the upland in developed and undeveloped watersheds were compared to study the impact of development on groundwater entering the marsh. Groundwater samples collected along the marsh perimeter were analyzed to study the impact of marsh width variability on groundwater quality within each creek. Preliminary results suggest a positive correlation between salinity and marsh width in undeveloped watersheds, and a higher concentration of nutrients in developed versus undeveloped watersheds.

Iron Isotope Variations in Reduced Groundwater and in Drinking Water Supplies: A Case Study of Hanoi, Vietnam

Science.gov (United States)

Teutsch, N.; Berg, M.; von Gunten, U.; Halliday, A.

2004-12-01

In reduced groundwater iron is involved in biotic and abiotic transformation processes, both of which could lead to iron isotope fractionation. The reduced groundwater aquifers in the area of the Vietnamese capital of Hanoi are the main drinking water sources for the city. These groundwaters contain arsenic, which imposes a serious health threat to millions of people. Dissolved arsenic is related to the reducing conditions prevalent in the groundwater, and iron and arsenic contents are correlated in the sediments. We are employing iron isotope composition as a tool to better understand the processes leading to the transformation of iron in the groundwater and its role in various biogeochemical processes in reduced environments. Drinking water is supplied to the city of Hanoi from several water treatment plants (WTP) which pump the raw groundwater from a lower aquifer, while the rural surroundings pump untreated groundwater from an upper aquifer by private tubewells. Surface water from the Red River delta is the main source of recharge to these two aquifers. Due to high content of particulate natural organic matter (NOM) in the sediment leading to extensive microbial activity, the groundwaters are anoxic and rich in dissolved iron(II). The iron(II) removal in the WTPs is carried by a multi-step treatment including aeration, settling, filtration, and chlorination. We have collected natural groundwater samples for isotopic analysis from two aquifers at several locations, a groundwater depth profile and its corresponding sediment phases from the upper aquifer and the underlying aquitard, raw and treated water from several WTPs, as well as the corresponding iron(III) precipitates. The iron concentrations of groundwaters analysed in this study range from 3 to 28 mg/L and δ 57Fe (57/54 deviation from IRMM 014) values vary between -1.2 and +1.5 ‰ . The sediment depth profile has a δ 57Fe around +0.3 ‰ , which implies that the high values obtained in the groundwater

Investigation of sulphide in core drilled boreholes KLX06, KAS03 and KAS09 at Laxemar and Aespoe Chemical-, microbiological- and dissolved gas data from groundwater in four borehole sections

Energy Technology Data Exchange (ETDEWEB)

Rosdahl, Anette (Geosigma AB (Sweden)); Pedersen, Karsten; Hallbeck, Lotta (Microbial Analytics Sweden AB (Sweden)); Wallin, Bill (Geokema AB (Sweden))

2011-01-15

This report describes a study performed during 2009 which focused on the production of sulphide (microbial sulphate reduction) in deep groundwater that was implemented in the core drilled boreholes KLX06, -475 to 482 meter above sea level, m a s l, KAS03,-97 to 241 and -613 to 984 m a s l, and KAS09, -96 to -125 m a s l, at Laxemar and Aspo. The study aimed to increase knowledge of background groundwater levels of sulphide and its variations in time and space through the analysis of sulphide and parameters related to sulphide production. Sampling of groundwater was conducted in three core drilled boreholes of varying age as time series with continuous pumping and as single samples. The analysis program covered chemical parameters (pH, chloride, sulphate, iron, and organic carbon), dissolved gas composition, stable isotopes in groundwater (delta2H, delta18O, delta34S, delta13C), stable isotopes of gaseous compounds (delta2H, delta13C, delta18O), microbiological parameters (sulphate- and iron reducing bacteria, SRB and IRB), phthalates and low molecular mass organic acids (LMMOA). The sampling in KLX06 was carried out as time series with a 9 week pause in pumping. When the water volume discharged was about 150 times that of the packer-isolated borehole section, sulphides decreased from 7 mg L-1 to 0.05 mg L-1 and the salinity increased from 740 to 1,480 mg L-1. After a 9 weeks pause in pumping, the sulphide concentration and salinity again approached the original values, i.e. 7 mg L-1 of sulphide and 450 mg L-1 of chloride. The SRB and IRB showed high concentrations that were reduced during pumping in the borehole. The water in the standpipe which has a different water composition than the groundwater, also showed similar high concentrations of sulphide and SRB. The standpipe is a plastic pipe in the wider upper part of the borehole; connected with the tube from the packer of the borehole section and used to accommodate a filter and a groundwater pump when collecting

Investigation of sulphide in core drilled boreholes KLX06, KAS03 and KAS09 at Laxemar and Aespoe: Chemical-, microbiological- and dissolved gas data from groundwater in four borehole sections

International Nuclear Information System (INIS)

Rosdahl, Anette; Pedersen, Karsten; Hallbeck, Lotta; Wallin, Bill

2011-01-01

This report describes a study performed during 2009 which focused on the production of sulphide (microbial sulphate reduction) in deep groundwater that was implemented in the core drilled boreholes KLX06, -475 to 482 meter above sea level, m a s l, KAS03,-97 to 241 and -613 to 984 m a s l, and KAS09, -96 to -125 m a s l, at Laxemar and Aspo. The study aimed to increase knowledge of background groundwater levels of sulphide and its variations in time and space through the analysis of sulphide and parameters related to sulphide production. Sampling of groundwater was conducted in three core drilled boreholes of varying age as time series with continuous pumping and as single samples. The analysis program covered chemical parameters (pH, chloride, sulphate, iron, and organic carbon), dissolved gas composition, stable isotopes in groundwater (δ 2 H, δ 18 O, δ 34 S, δ 13 C), stable isotopes of gaseous compounds (δ 2 H, δ 13 C, δ 18 O), microbiological parameters (sulphate- and iron reducing bacteria, SRB and IRB), phthalates and low molecular mass organic acids (LMMOA). The sampling in KLX06 was carried out as time series with a 9 week pause in pumping. When the water volume discharged was about 150 times that of the packer-isolated borehole section, sulphides decreased from 7 mg L -1 to 0.05 mg L -1 and the salinity increased from 740 to 1,480 mg L -1 . After a 9 weeks pause in pumping, the sulphide concentration and salinity again approached the original values, i.e. 7 mg L -1 of sulphide and 450 mg L -1 of chloride. The SRB and IRB showed high concentrations that were reduced during pumping in the borehole. The water in the standpipe which has a different water composition than the groundwater, also showed similar high concentrations of sulphide and SRB. The standpipe is a plastic pipe in the wider upper part of the borehole; connected with the tube from the packer of the borehole section and used to accommodate a filter and a groundwater pump when collecting

Geochemical modelling of grout-groundwater-rock interactions at the seal-rock interface

International Nuclear Information System (INIS)

Alcorn, S.; Christian-Frear, T.

1992-02-01

Theoretical investigations into the longevity of repository seals have dealt primarily with the development of a methodology to evaluate interactions between portland cement-based grout and groundwater. Evaluation of chemical thermodynamic equilibria among grout, groundwater, and granitic host rock phases using the geochemical codes EQ3NR/EQ6 suggests that a fracture filled with grout and saturated with groundwater will tend to fill and 'tighten' with time. These calculations predict that some grout and rock phases will dissolve, and that there will be precipitation of secondary phases which collectively have a larger overall volume than that of the material dissolved. Model assumptions include sealing of the fracture in a sluggish hydrologic regime (low gradient) characterized by a saline groundwater environment. The results of the calculations suggest that buffering of the fracture seals chemical system by the granitic rock may be important in determining the long-term fate of grout seals and the resulting phase assemblage in the fracture. The similarity of the predicted reaction product phases to those observed in naturally filled fractures suggests that with time equilibrium will be approached and grouted fractures subject to low hydrologic gradients will continue to seal. If grout injected into fractures materially reduces groundwater flux, the approach to chemical equilibrium will likely be accelerated. In light of this, even very thin or imperfectly grouted fractures would tighten in suitable hydrogeologic environments. In order to determine the period of time necessary to approach equilibrium, data on reaction rates are required. (au)

The role of groundwater discharge fluxes on Si:P ratios in a major tributary to Lake Erie.

Science.gov (United States)

Maavara, Taylor; Slowinski, Stephanie; Rezanezhad, Fereidoun; Van Meter, Kimberly; Van Cappellen, Philippe

2018-05-01

Groundwater discharge can be a major source of nutrients to river systems. Although quantification of groundwater nitrate loading to streams is common, the dependence of surface water silicon (Si) and phosphorus (P) concentrations on groundwater sources has rarely been determined. Additionally, the ability of groundwater discharge to drive surface water Si:P ratios has not been contextualized relative to riverine inputs or in-stream transformations. In this study, we quantify the seasonal dynamics of Si and P cycles in the Grand River (GR) watershed, the largest Canadian watershed draining into Lake Erie, to test our hypothesis that regions of Si-rich groundwater discharge increase surface water Si:P ratios. Historically, both the GR and Lake Erie have been considered stoichiometrically P-limited, where the molar Si:P ratio is greater than the ~16:1 phytoplankton uptake ratio. However, recent trends suggest that eastern Lake Erie may be approaching Si-limitation. We sampled groundwater and surface water for dissolved and reactive particulate Si as well as total dissolved P for 12months within and downstream of a 50-km reach of high groundwater discharge. Our results indicate that groundwater Si:P ratios are lower than the corresponding surface water and that groundwater is a significant source of bioavailable P to surface water. Despite these observations, the watershed remains P-limited for the majority of the year, with localized periods of Si-limitation. We further find that groundwater Si:P ratios are a relatively minor driver of surface water Si:P, but that the magnitude of Si and P loads from groundwater represent a large proportion of the overall fluxes to Lake Erie. Copyright © 2017 Elsevier B.V. All rights reserved.

1997 Comprehensive TNX Area Annual Groundwater and Effectiveness Monitoring Report

International Nuclear Information System (INIS)

Chase, J.

1998-04-01

Shallow groundwater beneath the TNX Area at the Savannah River Site (SRS) has been contaminated with chlorinated volatile organic compounds (CVOCs) such as trichloroethylene (TCE) and carbon tetrachloride. In November 1994, an Interim Record of Decision (IROD) was agreed to and signed by the U. S. Department of Energy (DOE), the Environmental Protection Agency (EPA), and the South Carolina Department of Health ampersand Environmental Control (SCDHEC). The Interim Record of Decision requires the installation of a hybrid groundwater corrective action (HGCA) to stabilize the plume of groundwater contamination and remove CVOCs dissolved in the groundwater. The hybrid groundwater corrective action included a recovery well network, purge water management facility, air stripper, and an airlift recirculation well. The recirculation well was dropped pursuant to a test that indicated it to be ineffective at the TNX Area. Consequently, the groundwater corrective action was changed from a hybrid to a single action, pump-and-treat approach. The Interim Action (IA) T-1 air stripper system began operation on September 16, 1996. a comprehensive groundwater monitoring program was initiated to measure the effectiveness of the system. As of December 31, 1997, the system has treated 32 million gallons of contaminated groundwater removed 32 pounds of TCE. The recovery well network created a 'capture zone' that stabilized the plume of contaminated groundwater

1997 Comprehensive TNX Area Annual Groundwater and Effectiveness Monitoring Report

Energy Technology Data Exchange (ETDEWEB)

Chase, J.

1998-04-01

Shallow groundwater beneath the TNX Area at the Savannah River Site (SRS) has been contaminated with chlorinated volatile organic compounds (CVOCs) such as trichloroethylene (TCE) and carbon tetrachloride. In November 1994, an Interim Record of Decision (IROD) was agreed to and signed by the U. S. Department of Energy (DOE), the Environmental Protection Agency (EPA), and the South Carolina Department of Health {ampersand} Environmental Control (SCDHEC). The Interim Record of Decision requires the installation of a hybrid groundwater corrective action (HGCA) to stabilize the plume of groundwater contamination and remove CVOCs dissolved in the groundwater. The hybrid groundwater corrective action included a recovery well network, purge water management facility, air stripper, and an airlift recirculation well. The recirculation well was dropped pursuant to a test that indicated it to be ineffective at the TNX Area. Consequently, the groundwater corrective action was changed from a hybrid to a single action, pump-and-treat approach. The Interim Action (IA) T-1 air stripper system began operation on September 16, 1996. a comprehensive groundwater monitoring program was initiated to measure the effectiveness of the system. As of December 31, 1997, the system has treated 32 million gallons of contaminated groundwater removed 32 pounds of TCE. The recovery well network created a `capture zone` that stabilized the plume of contaminated groundwater.

Coupled S and Sr isotope evidences for elevated arsenic concentrations in groundwater from the world's largest antimony mine, Central China

Science.gov (United States)

Wen, Bing; Zhou, Aiguo; Zhou, Jianwei; Liu, Cunfu; Huang, Yuliu; Li, Ligang

2018-02-01

The Xikuangshan(XKS) mine, the world's largest antimony mine, was chosen for a detailed arsenic hydrogeochemical study because of the elevated arsenic in bedrock aquifers used by local residents. Hydrochemical data, δ34S values of dissolved SO42- and 87Sr/86Sr ratios have been analyzed to identify the predominant geochemical processes that control the arsenic mobilization within the aquifers. Groundwater samples can be divided into three major types: low arsenic groundwater (0-50 μg/L), high arsenic groundwater (50-1000 μg/L) and anomalous high arsenic groundwater (>1000 μg/L). Arsenic occurs under oxidizing conditions at the XKS Sb mine as the HAsO42- anion. The Ca/Na ratio correlates significantly with HCO3-/Na and Sr/Na ratios, indicating that carbonate dissolution and silicate weathering are the dominant processes controlling groundwater hydrochemistry. The δ34S values of the groundwater indicate that dissolved SO42- in groundwater is mainly sourced from the oxidation of sulfide minerals, and elevated As concentrations in groundwater are influenced by the mixing of mine water and surface water. Furthermore, the δ34S values are not correlated with dissolved As concentrations and Fe concentrations, suggesting that the reduction dissolution of Fe(III) hydroxides is not the dominant process controlling As mobilization. The 87Sr/86Sr ratios imply that elevated As concentrations in groundwater are primarily derived from the interaction with the stibnite and silicified limestone. More specifically, the excess-Na ion, the feature of Ca/Na ratio, and the spatial association of elevated As concentrations in groundwater collectively suggest that high and anomalous high arsenic groundwater are associated with smelting slags and, in particular, the arsenic alkali residue. In general, the hydrochemistry analysis, especially the S and Sr isotope evidences elucidate that elevated As concentrations and As mobilization are influenced by several geochemical processes

Natural radioactivity in groundwater from the south-eastern Arabian Peninsula and environmental implications

DEFF Research Database (Denmark)

Murad, A.; Zhou, X. D.; Yi, P.

2014-01-01

increase the radioactivity in the groundwater. This conclusion is also supported by the positive correlation between radioactivity and amount of total dissolved solid. Particular water purification technology and environmental impact assessments are essential for sustainable and secure use...

Removal of dissolved organic matter in municipal effluent with ozonation, slow sand filtration and nanofiltration as high quality pre-treatment option for artificial groundwater recharge.

Science.gov (United States)

Linlin, Wu; Xuan, Zhao; Meng, Zhang

2011-04-01

In the paper the combination process of ozonation, slow sand filtration (SSF) and nanofiltration (NF) was investigated with respect to dissolved organic matter (DOM) removal as high quality pre-treatment option for artificial groundwater recharge. With the help of ozonation leading to breakdown of the large organic molecules, SSF preferentially removes soluble microbial by-product-like substances and DOM with molecular weight (MW) less than 1.0 kDa. NF, however, removes aromatic, humic acid-like and fulvic acid-like substances efficiently and specially removes DOM with MW above 1.0 kDa. The residual DOM of the membrane permeate is dominated by small organics with MW 500 Da, which can be further reduced by the aquifer treatment, despite of the very low concentration. Consequently, the O(3)/SSF/NF system offers a complementary process in DOM removal. Dissolved organic carbon (DOC) and trihalomethane formation potential (THMFP) can be reduced from 6.5±1.1 to 0.7±0.3 mg L(-1) and from 267±24 to 52±6 μg L(-1), respectively. The very low DOC concentration of 0.6±0.2 mg L(-1) and THMFP of 44±4 μg L(-1) can be reached after the aquifer treatment. Copyright © 2011 Elsevier Ltd. All rights reserved.

Genesis of the gossan at the Las Cruces Ore Deposit (SW Spain). Groundwater-Rock Interaction.

Science.gov (United States)

Scheiber, L.; Ayora, C.; Vázquez-Suñé, E.; Soler, A.

2016-12-01

The Las Cruces deposit has sparked an interest in the scientific community due to the exceptional genesis and mineralogical composition. The original gossan formed by goethite and hematite has been replaced by siderite and galena rock. The current gossan composition is as the result of the interaction of groundwater that circulates through the Niebla-Posadas aquifer and a gossan formed by Fe-oxyhydroxides. The groundwater conditions promoted the reductive dissolution of Pb-bearing goethite by the organic matter degradation and the formation of siderite and galena. Hydrochemical and isotopic characteristics of groundwater endorses this hypothesis. Thus, negative Eh values, the existence of H2S and the tendency to light sulfate isotope values show the reducing conditions of groundwater. The key role of the organic matter degradation is marked by the high ammonium, boron and dissolved organic carbon (DOC) concentrations together the light δ13C values, both in groundwater and siderite. The siderite precipitation is confirmed by the high pH values (up to 10), the low amount of Fe (<10ppb) and the thermodynamic calculations. The Fe-oxyhydroxides are a high adsorption capacity which is capable of absorbing metals as arsenic, lead and antimony. The reductive dissolution of these minerals involves the release of these metal to groundwater. Then, the groundwater rich in sulfur and an excess of lead produce the galena precipitation. The likeness between the δ34S values, both the gossan and groundwater, reveals that the sulfur of the galena come from the currently groundwater. A reactive transport model confirm that the present day groundwater flux and composition is able to form the siderite rock in less than 1Ma, with no external supply of reactants. The limiting factor of the process is the Dissolved Organic Carbon (DOC) concentration in groundwater, i.e., higher concentrations would decrease the formation time, whereas the result is not sensitive to flow conditions.

Summertime calcium carbonate undersaturation in shelf waters of the western Arctic Ocean – how biological processes exacerbate the impact of ocean acidification

OpenAIRE

N. R. Bates; M. I. Orchowska; R. Garley; J. T. Mathis

2013-01-01

The Arctic Ocean accounts for only 4% of the global ocean area, but it contributes significantly to the global carbon cycle. Recent observations of seawater CO2-carbonate chemistry in shelf waters of the western Arctic Ocean, primarily in the Chukchi Sea, from 2009 to 2011 indicate that bottom waters are seasonally undersaturated with respect to calcium carbonate (CaCO3) minerals, particularly aragonite. Nearly 40% of sampled bottom waters on the shelf have saturation states...

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.

Carbon isotope systematics of the Cambrian–Vendian aquifer system in the northern Baltic Basin: Implications to the age and evolution of groundwater

International Nuclear Information System (INIS)

Raidla, Valle; Kirsimäe, Kalle; Vaikmäe, Rein; Kaup, Enn; Martma, Tõnu

2012-01-01

Groundwater in the Cambrian–Vendian aquifer system has a strongly depleted stable isotope composition (δ 18 O values of about −22‰) and a low radiocarbon concentration, which suggests that the water is of glacial origin from the last Ice Age. The aim of this paper was to elucidate the timing of infiltration of glacial waters and to understand the geochemical evolution of this groundwater. The composition of the dissolved inorganic C (DIC) in Cambrian–Vendian groundwater is influenced by complex reactions and isotope exchange processes between water, organic materials and rock matrix. The δ 13 C composition of dissolved inorganic C in Cambrian–Vendian water also indicates a bacterial modification of the isotope system. The corrected radiocarbon ages of groundwater are between 14,000 and 27,000 radiocarbon years, which is coeval with the advance of the Weichselian Glacier in the area.

Size-fractionation of groundwater arsenic in alluvial aquifers of West Bengal, India: the role of organic and inorganic colloids.

Science.gov (United States)

Majumder, Santanu; Nath, Bibhash; Sarkar, Simita; Chatterjee, Debashis; Roman-Ross, Gabriela; Hidalgo, Manuela

2014-01-15

Dissolved organic carbon (DOC) and Fe mineral phases are known to influence the mobility of arsenic (As) in groundwater. Arsenic can be associated with colloidal particles containing organic matter and Fe. Currently, no data is available on the dissolved phase/colloidal association of As in groundwater of alluvial aquifers in West Bengal, India. This study investigated the fractional distribution of As (and other metals/metalloids) among the particulate, colloidal and dissolved phases in groundwater to decipher controlling behavior of organic and inorganic colloids on As mobility. The result shows that 83-94% of As remained in the 'truly dissolved' phases (i.e., 0.05 μm size) colloidal particles, which indicates the close association of As with larger Fe-rich inorganic colloids. In smaller (i.e., <0.05 μm size) colloidal particles strong positive correlation is observed between As and DOC (r(2)=0.85), which highlights the close association of As with smaller organic colloids. As(III) is mainly associated with larger inorganic colloids, whereas, As(V) is associated with smaller organic/organometallic colloids. Scanning Electron Microscopy and Energy Dispersive X-ray spectroscopy confirm the association of As with DOC and Fe mineral phases suggesting the formation of dissolved organo-Fe complexes and colloidal organo-Fe oxide phases. Attenuated total reflectance-Fourier transform infrared spectroscopy further confirms the formation of As-Fe-NOM organometallic colloids, however, a detailed study of these types of colloids in natural waters is necessary to underpin their controlling behavior. © 2013 Elsevier B.V. All rights reserved.

Evaluating hydrochemical data from shallow groundwater in Laxemar from a microbiological perspective

Energy Technology Data Exchange (ETDEWEB)

Hallbeck, Lotta (Microbial Analytics Sweden AB, Goeteborg (Sweden))

2008-01-15

Oxygen is one of the chemical species that can corrode a copper canister in a KBS-3 repository. It is therefore important to determine whether oxygen dissolved in precipitation or groundwater could reach repository depth by means of groundwater transport. This can be determined by gaining an understanding of the oxygen-consuming microbial processes that take place in shallow groundwater in the area of interest. This report evaluates hydrogeochemical data from shallow groundwater in the Laxemar area from a microbiological perspective. Hydrogeochemical data were gathered from soil pipes at depths from 1.6 to 16.5 m and from percussion-drilled boreholes having mid-point depths of between 28.5 and 131 m. Only a few of the percussion-drilled boreholes had packers installed; the sampled sections were therefore very extended, allowing groundwaters from many different depths to mix. Oxygen and oxygen reduction potential (ORP) were not measured in groundwater from soil pipes or percussion drilled boreholes. The report therefore focuses on parameters that indicated ongoing anaerobic microbial processes, such as nitrite, ferrous iron, dissolved manganese, and sulphide, that were found in many soil pipes. Even though many of the soil pipes were located in similar environments and at relatively similar depths, ranging from 3.5 to 6 m, they displayed individual chemical profiles in terms of chemical species related to microbial activity. The microbial activity could not be linked to the classes of soil pipe, i.e. recharge, discharge, or intermittent. Existing soil pipes and percussion-drilled boreholes could be used for additional sampling to measure microbial parameters. Such sampling would benefit from the careful hypothesis-driven description of the sampling parameters and experience-guided choice of sampling methods

Evaluating hydrochemical data from shallow groundwater in Laxemar from a microbiological perspective

International Nuclear Information System (INIS)

Hallbeck, Lotta

2008-01-01

Oxygen is one of the chemical species that can corrode a copper canister in a KBS-3 repository. It is therefore important to determine whether oxygen dissolved in precipitation or groundwater could reach repository depth by means of groundwater transport. This can be determined by gaining an understanding of the oxygen-consuming microbial processes that take place in shallow groundwater in the area of interest. This report evaluates hydrogeochemical data from shallow groundwater in the Laxemar area from a microbiological perspective. Hydrogeochemical data were gathered from soil pipes at depths from 1.6 to 16.5 m and from percussion-drilled boreholes having mid-point depths of between 28.5 and 131 m. Only a few of the percussion-drilled boreholes had packers installed; the sampled sections were therefore very extended, allowing groundwaters from many different depths to mix. Oxygen and oxygen reduction potential (ORP) were not measured in groundwater from soil pipes or percussion drilled boreholes. The report therefore focuses on parameters that indicated ongoing anaerobic microbial processes, such as nitrite, ferrous iron, dissolved manganese, and sulphide, that were found in many soil pipes. Even though many of the soil pipes were located in similar environments and at relatively similar depths, ranging from 3.5 to 6 m, they displayed individual chemical profiles in terms of chemical species related to microbial activity. The microbial activity could not be linked to the classes of soil pipe, i.e. recharge, discharge, or intermittent. Existing soil pipes and percussion-drilled boreholes could be used for additional sampling to measure microbial parameters. Such sampling would benefit from the careful hypothesis-driven description of the sampling parameters and experience-guided choice of sampling methods

Arsenic mineral dissolution and possible mobilization in mineral–microbe–groundwater environment

International Nuclear Information System (INIS)

Islam, A.B.M.R.; Maity, Jyoti Prakash; Bundschuh, Jochen; Chen, Chien-Yen; Bhowmik, Bejon Kumar; Tazaki, Kazue

2013-01-01

Highlights: ► Bacteria use arsenic minerals for their growth without supplementary nutrient. ► Enzymatically active bacteria survive in the arsenic contaminated environment. ► Mostly bacillus, coccus and filamentous dissolves the arsenic mineral. ► Except enargite, soluble-As was detected with respect to other arsenic mineral. ► Dissolution: native-As > arsenolite > orpiment > realgar > arsenopyrite > tennantite. -- Abstract: Arsenic (As) is widely distributed in the nature as ores or minerals. It has been attracted much attention for the global public health issue, especially for groundwater As contamination. The aim of this study was to elucidate the characteristics of microbes in groundwater where As-minerals were dissolved. An ex situ experiment was conducted with 7 standard As-minerals in bacteria-free groundwater and stored in experimental vessels for 1 year without supplementary nutrients. The pH (6.7–8.4) and Eh S.H.E. (24–548 mV) changed between initial (0 day) and final stages (365 days) of experiment. The dissolution of As was detected higher from arsenolite (4240 ± 8.69 mg/L) and native arsenic (4538 ± 9.02 mg/L), whereas moderately dissolved from orpiment (653 ± 3.56 mg/L) and realgar (319 ± 2.56 mg/L) in compare to arsenopyrite (85 ± 1.25 mg/L) and tennantite (3 ± 0.06 mg/L). Optical microscopic, scanning electron microscopic observations and flurometric enumeration revealed the abundance of As-resistant bacillus, coccus and filamentous types of microorganisms on the surface of most of As-mineral. 4′-6-Diamidino-2-phenylindole (DAPI)-stained epifluorescence micrograph confirmed the presence of DNA and carboxyfluorescein diacetate (CFDA) staining method revealed the enzymatically active bacteria on the surface of As-minerals such as in realgar (As 4 S 4 ). Therefore, the microbes enable to survive and mobilize the As in groundwater by dissolution/bioweathering of As-minerals

Arsenic mineral dissolution and possible mobilization in mineral–microbe–groundwater environment

Energy Technology Data Exchange (ETDEWEB)

Islam, A.B.M.R., E-mail: uttambangla@yahoo.com [Department of Human Ecology, School of International Health, Graduate School of Medicine, The University of Tokyo,7-3-1, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan); ITO Public Nuisance Research Institute, 1-26-8, Omori Kita, Otaku, Tokyo 142-0016 (Japan); Maity, Jyoti Prakash, E-mail: jyoti_maity@yahoo.com [Department of Earth and Environmental Sciences, National Chung Cheng University, 168 University Road, Ming-Shung, Chiayi County 62102, Taiwan (China); Bundschuh, Jochen [Faculty of Engineering and Surveying, University of Southern Queensland, Toowoomba, Queensland 435 (Australia); KTH-International Groundwater Arsenic Research Group, Department of Land and Water Resources Engineering, Royal Institute of Technology (KTH) Teknikringen 76,SE-10044 Stockholm (Sweden); Department of Earth Sciences, National Cheng Kung University, University Road, Tainan, 70101, Taiwan (China); Chen, Chien-Yen [Department of Earth and Environmental Sciences, National Chung Cheng University, 168 University Road, Ming-Shung, Chiayi County 62102, Taiwan (China); Bhowmik, Bejon Kumar [Department of Biotechnology, Graduate School of Agriculture and Life science, The University of Tokyo, 1-1-1,Yayoi, Bunkyo-ku, Tokyo 113-0033 (Japan); Tazaki, Kazue [Department of Earth Sciences, Faculty of Science, Kanazawa University, Kakuma, Kanazawa, Ishikawa 920-1192 (Japan)

2013-11-15

Highlights: ► Bacteria use arsenic minerals for their growth without supplementary nutrient. ► Enzymatically active bacteria survive in the arsenic contaminated environment. ► Mostly bacillus, coccus and filamentous dissolves the arsenic mineral. ► Except enargite, soluble-As was detected with respect to other arsenic mineral. ► Dissolution: native-As > arsenolite > orpiment > realgar > arsenopyrite > tennantite. -- Abstract: Arsenic (As) is widely distributed in the nature as ores or minerals. It has been attracted much attention for the global public health issue, especially for groundwater As contamination. The aim of this study was to elucidate the characteristics of microbes in groundwater where As-minerals were dissolved. An ex situ experiment was conducted with 7 standard As-minerals in bacteria-free groundwater and stored in experimental vessels for 1 year without supplementary nutrients. The pH (6.7–8.4) and Eh{sub S.H.E.} (24–548 mV) changed between initial (0 day) and final stages (365 days) of experiment. The dissolution of As was detected higher from arsenolite (4240 ± 8.69 mg/L) and native arsenic (4538 ± 9.02 mg/L), whereas moderately dissolved from orpiment (653 ± 3.56 mg/L) and realgar (319 ± 2.56 mg/L) in compare to arsenopyrite (85 ± 1.25 mg/L) and tennantite (3 ± 0.06 mg/L). Optical microscopic, scanning electron microscopic observations and flurometric enumeration revealed the abundance of As-resistant bacillus, coccus and filamentous types of microorganisms on the surface of most of As-mineral. 4′-6-Diamidino-2-phenylindole (DAPI)-stained epifluorescence micrograph confirmed the presence of DNA and carboxyfluorescein diacetate (CFDA) staining method revealed the enzymatically active bacteria on the surface of As-minerals such as in realgar (As{sub 4}S{sub 4}). Therefore, the microbes enable to survive and mobilize the As in groundwater by dissolution/bioweathering of As-minerals.

Preliminary assessment of water chemistry related to groundwater flooding in Wawarsing, New York, 2009-11

Science.gov (United States)

Brown, Craig J.; Eckhardt, David A.; Stumm, Frederick; Chu, Anthony

2012-01-01

Water-quality samples collected in an area prone to groundwater flooding in Wawarsing, New York, were analyzed and assessed to better understand the hydrologic system and to aid in the assessment of contributing water sources. Above average rainfall over the past decade, and the presence of a pressurized water tunnel that passes about 700 feet beneath Wawarsing, could both contribute to groundwater flooding. Water samples were collected from surface-water bodies, springs, and wells and analyzed for major and trace inorganic constituents, dissolved gases, age tracers, and stable isotopes. Distinct differences in chemistry exist between tunnel water and groundwater in unconsolidated deposits and in bedrock, and among groundwater samples collected from some bedrock wells during high head pressure and low head pressure of the Rondout-West Branch Tunnel. Samples from bedrock wells generally had relatively higher concentrations of sulfate (SO42-), strontium (Sr), barium (Ba), and lower concentrations of calcium (Ca) and bicarbonate (HCO3-), as compared to unconsolidated wells. Differences in stable-isotope ratios among oxygen-18 to oxygen-16 (δ18O), hydrogen-2 to hydrogen-1 (δ2H), sulfur-34 to sulfur-32(δ34S) of SO42-, Sr-87 to Sr-86 (87Sr/86Sr), and C-13 to C-12 (δ13C) of dissolved inorganic carbon (DIC) indicate a potential for distinguishing water in the Delaware-West Branch Tunnel from native groundwater. For example, 87Sr/86Sr ratios were more depleted in groundwater samples from most bedrock wells, as compared to samples from surface-water sources, springs, and wells screened in unconsolidated deposits in the study area. Age-tracer data provided useful information on pathways of the groundwater-flow system, but were limited by inherent problems with dissolved gases in bedrock wells. The sulfur hexafluoride (SF6) and (or) chlorofluorocarbons (CFCs) apparent recharge years of most water samples from wells screened in unconsolidated deposits and springs ranged

Effects of residential wastewater treatment systems on ground-water quality in west-central Jefferson County, Colorado

Science.gov (United States)

Hall, Dennis C.; Hillier, D.E.; Nickum, Edward; Dorrance, W.G.

1981-01-01

The use of residential wastewater-treatment systems in Evergreen Meadows, Marshdale, and Herzman Mesa, Colo., has degraded ground-water quality to some extent in each community. Age of community; average lot size; slope of land surface; composition, permeability, and thickness of surficial material; density, size , and orientation of fractures; maintenance of wastewater-treatment systems; and presence of animals are factors possibly contributing to the degradation of ground-water quality. When compared with effluent from aeration-treatment tanks, effluent fom septic-treatment tanks is characterized by greater biochemical oxygen demand and greater concentrations of detergents. When compared with effluent from septic-treatment tanks, effluent from aeration-treatment tanks is characterized by greater concentrations of dissolved oxygen, nitrite, nitrate, sulfate, and dissolved solids. (USGS)

In situ treatment of arsenic-contaminated groundwater by air sparging.

Science.gov (United States)

Brunsting, Joseph H; McBean, Edward A

2014-04-01

Arsenic contamination of groundwater is a major problem in some areas of the world, particularly in West Bengal (India) and Bangladesh where it is caused by reducing conditions in the aquifer. In situ treatment, if it can be proven as operationally feasible, has the potential to capture some advantages over other treatment methods by being fairly simple, not using chemicals, and not necessitating disposal of arsenic-rich wastes. In this study, the potential for in situ treatment by injection of compressed air directly into the aquifer (i.e. air sparging) is assessed. An experimental apparatus was constructed to simulate conditions of arsenic-rich groundwater under anaerobic conditions, and in situ treatment by air sparging was employed. Arsenic (up to 200 μg/L) was removed to a maximum of 79% (at a local point in the apparatus) using a solution with dissolved iron and arsenic only. A static "jar" test revealed arsenic removal by co-precipitation with iron at a molar ratio of approximately 2 (iron/arsenic). This is encouraging since groundwater with relatively high amounts of dissolved iron (as compared to arsenic) therefore has a large theoretical treatment capacity for arsenic. Iron oxidation was significantly retarded at pH values below neutral. In terms of operation, analysis of experimental results shows that periodic air sparging may be feasible. Copyright © 2014 Elsevier B.V. All rights reserved.

Mixing-induced groundwater denitrification beneath a manured field in southern Alberta, Canada

International Nuclear Information System (INIS)

McCallum, J.E.; Ryan, M.C.; Mayer, B.; Rodvang, S.J.

2008-01-01

Contamination of shallow groundwater by NO 3 - from manure may occur under fields where manure is spread as fertilizer and for disposal. Attenuation of NO 3 - in groundwater occurs through denitrification under certain conditions, or NO 3 - -contaminated younger groundwater may mix with older groundwater, lowering the NO 3 - concentration. In this study, δ 15 N and δ 18 O values of NO 3 - , and δ 18 O and δ 2 H values in groundwater under a manured field were evaluated to determine if groundwater NO 3 - concentrations were influenced through mixing of shallower, manure-impacted groundwater with older groundwater, or if denitrification was reducing NO 3 - concentrations. The younger groundwater showed clear evidence of manure impact with elevated Cl - (∼85 mg L -1 ) and NO 3 - concentrations (∼50 mg NO 3 -N L -1 ), and δ 15 N and δ 18 O values of NO 3 - consistent with a manure source. Vertical hydraulic gradients and δ 18 O and δ 2 H values in groundwater suggest older, more reduced groundwater is upwelling locally and mixing with the shallow groundwater. Decreasing NO 3 :Cl ratios, decreasing dissolved O 2 concentrations, and increasing δ 15 N and δ 18 O values of NO 3 - suggest that denitrification occurs locally in the aquifer. The extent of denitrification is proportional to the fraction of deeper groundwater in the aquifer. Denitrification apparently does not proceed in the younger, manure-impacted groundwater in the absence of mixing

Assessing the relative bioavailability of DOC in regional groundwater systems

Science.gov (United States)

Chapelle, Francis H.; Bradley, Paul M.; Journey, Celeste A.; McMahon, Peter B.

2013-01-01

It has been hypothesized that the degree to which a hyperbolic relationship exists between concentrations of dissolved organic carbon (DOC) and dissolved oxygen (DO) in groundwater may indicate the relative bioavailability of DOC. This hypothesis was examined for 73 different regional aquifers of the United States using 7745 analyses of groundwater compiled by the National Water Assessment (NAWQA) program of the U.S. Geological Survey. The relative reaction quotient (RRQ), a measure of the curvature of DOC concentrations plotted versus DO concentrations and regressed to a decaying hyperbolic equation, was used to assess the relative bioavailability of DOC. For the basalt aquifer of Oahu, Hawaii, RRQ values were low (0.0013 mM−2), reflecting a nearly random relationship between DOC and DO concentrations. In contrast, on the island of Maui, treated sewage effluent injected into a portion of the basalt aquifer resulted in pronounced hyperbolic DOC-DO behavior and a higher RRQ (142 mM−2). RRQ values for the 73 aquifers correlated positively with mean concentrations of ammonia, dissolved iron, and manganese, and correlated negatively with mean pH. This indicates that greater RRQ values are associated with greater concentrations of the final products of microbial reduction reactions. RRQ values and DOC concentrations were negatively correlated with the thickness of the unsaturated zone (UNST) and depth to the top of the screened interval. Finally, RRQ values were positively correlated with mean annual precipitation (MAP), and the highest observed RRQ values were associated with aquifers receiving MAP rates ranging between 900 and 1300 mm/year. These results are uniformly consistent with the hypothesis that the hyperbolic behavior of DOC-DO plots, as quantified by the RRQ metric, can be an indicator of relative DOC bioavailability in groundwater systems.

Assessing the relative bioavailability of DOC in regional groundwater systems.

Science.gov (United States)

Chapelle, Francis H; Bradley, Paul M; Journey, Celeste A; McMahon, Peter B

2013-01-01

It has been hypothesized that the degree to which a hyperbolic relationship exists between concentrations of dissolved organic carbon (DOC) and dissolved oxygen (DO) in groundwater may indicate the relative bioavailability of DOC. This hypothesis was examined for 73 different regional aquifers of the United States using 7745 analyses of groundwater compiled by the National Water Assessment (NAWQA) program of the U.S. Geological Survey. The relative reaction quotient (RRQ), a measure of the curvature of DOC concentrations plotted versus DO concentrations and regressed to a decaying hyperbolic equation, was used to assess the relative bioavailability of DOC. For the basalt aquifer of Oahu, Hawaii, RRQ values were low (0.0013 mM(-2)), reflecting a nearly random relationship between DOC and DO concentrations. In contrast, on the island of Maui, treated sewage effluent injected into a portion of the basalt aquifer resulted in pronounced hyperbolic DOC-DO behavior and a higher RRQ (142 mM(-2)). RRQ values for the 73 aquifers correlated positively with mean concentrations of ammonia, dissolved iron, and manganese, and correlated negatively with mean pH. This indicates that greater RRQ values are associated with greater concentrations of the final products of microbial reduction reactions. RRQ values and DOC concentrations were negatively correlated with the thickness of the unsaturated zone (UNST) and depth to the top of the screened interval. Finally, RRQ values were positively correlated with mean annual precipitation (MAP), and the highest observed RRQ values were associated with aquifers receiving MAP rates ranging between 900 and 1300 mm/year. These results are uniformly consistent with the hypothesis that the hyperbolic behavior of DOC-DO plots, as quantified by the RRQ metric, can be an indicator of relative DOC bioavailability in groundwater systems. Published 2012. This article is a U.S. Government work and is in the public domain in the USA.

Water-carbon Links in a Tropical Forest: How Interbasin Groundwater Flow Affects Carbon Fluxes and Ecosystem Carbon Budgets

Energy Technology Data Exchange (ETDEWEB)

Genereux, David [North Carolina State Univ., Raleigh, NC (United States); Osburn, Christopher [North Carolina State Univ., Raleigh, NC (United States); Oberbauer, Steven [Florida Intl Univ., Miami, FL (United States); Oviedo Vargas, Diana [North Carolina State Univ., Raleigh, NC (United States); Dierick, Diego [Florida Intl Univ., Miami, FL (United States)

2017-03-27

This report covers the outcomes from a quantitative, interdisciplinary field investigation of how carbon fluxes and budgets in a lowland tropical rainforest are affected by the discharge of old regional groundwater into streams, springs, and wetlands in the forest. The work was carried out in a lowland rainforest of Costa Rica, at La Selva Biological Station. The research shows that discharge of regional groundwater high in dissolved carbon dioxide represents a significant input of carbon to the rainforest "from below", an input that is on average larger than the carbon input "from above" from the atmosphere. A stream receiving discharge of regional groundwater had greatly elevated emissions of carbon dioxide (but not methane) to the overlying air, and elevated downstream export of carbon from its watershed with stream flow. The emission of deep geological carbon dioxide from stream water elevates the carbon dioxide concentrations in air above the streams. Carbon-14 tracing revealed the presence of geological carbon in the leaves and stems of some riparian plants near streams that receive inputs of regional groundwater. Also, discharge of regional groundwater is responsible for input of dissolved organic matter with distinctive chemistry to rainforest streams and wetlands. The discharge of regional groundwater in lowland surface waters has a major impact on the carbon cycle in this and likely other tropical and non-tropical forests.

Natural organics in groundwaters and their potential effect on contaminant transport in granitic rock

International Nuclear Information System (INIS)

Vilks, P.; Bachinski, D.B.; Richer, D.

1996-07-01

Naturally occurring organics in groundwaters of the Whiteshell Research Area (WRA) of southern Manitoba and of the Atikokan Research Area of northwestern Ontario were investigated to assess their potential role in radionuclide transport within granite fractures of the Canadian Shield. A survey of dissolved organic carbon (DOC) concentrations, carried out to determine the variability in the organic content of these groundwaters, showed average concentrations in WRA deep groundwaters of 0.8 ± 0.1 mg/L for Fracture Zone 2, 0.8 ± 0.4 mg/L for near-vertical fractures, and 2.3 ± 0.8 mg/L for deeper saline groundwater. Surface waters and near-surface groundwaters had significantly higher DOC with 29.2 ± 0.6 mg/L in streams from the East Swamp. The DOC consisted mainly of hydrophilic neutral compounds 60 to 75%, and hydrophobic and hydrophilic acids 23 to 39%, along with very small amounts of hydrophobic bases and neutrals, and hydrophilic bases. The average complexing capacity of natural organics in WRA deep groundwaters was calculated to be 6.7 x 10 -6 eq/L. The ability of these organics to complex radionuclides was tested using conditional stability constants from the literature for humic complex formation with trivalent, tetravalent, pentavalent and hexavalent actinides. The chemistries of Np(V) and U(VI) were predicted to be dominated by inorganic complexes and not significantly affected by organics. Accurate predictions for AM(III) and Th(IV) could not be made since the literature contains a wide range in values of stability constants for humic complexes with these elements. Surface waters and near-surface groundwaters in many areas of the Canadian Shield contain enough humics to complex a significant fraction of dissolved actinides. Radiocarbon ages of humics from WRA groundwater varied between 3600 and 6200 years before present, indicating that a component of humic substances in deep groundwaters must originate from near-surface waters. 54 refs., 15 tabs., 5

Estimation of groundwater residence time and evaluation of geomorphological processes using cosmogenic and terrigenic radionuclides and isotopes of noble gases

International Nuclear Information System (INIS)

Mahara, Yasunori; Ohta, Tomoko; Igarashi, Toshifumi

2013-01-01

In this paper, the estimation of groundwater residence time and geomorphological changing processes are discussed by focusing on isotopes of noble gases and radionuclides with a long half-life as an environmental tracer. Noble gases and radionuclides are produced in the atmospheric air and terrestrial rocks by spallation and various muon reactions during cosmic rays irradiation. Groundwater dating and geomorphological changing are estimated from changes in the number of atoms of cosmogenic and terrigenic nuclides in groundwater and terrestrial rock. The main tools of groundwater dating are combination of the dissolved helium and tritium (half-life T 1/2 =12.3 y) for younger groundwater less than 60 years of residence time, and of the dissolved helium and 36 Cl (T 1/2 =3.01 x 10 5 y) for older groundwater over million years. On the other hand, the main tools on the geomorphological changes are the estimation of exposure time using cosmogenic radionuclides ( 10 Be(half-life T 1/2 =1.6 x 10 6 y), 14 C (T 1/2 =5730 y), 26 Al (T 1/2 =7.16 x 10 5 y) and 36 Cl) and cosmogenic stable noble gases ( 3 He and 21 Ne) produced in rock. (author)

Cl/Br ratios and chlorine isotope evidences for groundwater salinization and its impact on groundwater arsenic, fluoride and iodine enrichment in the Datong basin, China

Energy Technology Data Exchange (ETDEWEB)

Li, Junxia; Wang, Yanxin, E-mail: yx.wang@cug.edu.cn; Xie, Xianjun

2016-02-15

In order to identify the salinization processes and its impact on arsenic, fluoride and iodine enrichment in groundwater, hydrogeochemical and environmental isotope studies have been conducted on groundwater from the Datong basin, China. The total dissolved solid (TDS) concentrations in groundwater ranged from 451 to 8250 mg/L, and 41% of all samples were identified as moderately saline groundwater with TDS of 3000–10,000 mg/L. The results of groundwater Cl concentrations, Cl/Br molar ratio and Cl isotope composition suggest that three processes including water-rock interaction, surface saline soil flushing, and evapotranspiration result in the groundwater salinization in the study area. The relatively higher Cl/Br molar ratio in groundwater from multiple screening wells indicates the contribution of halite dissolution from saline soil flushed by vertical infiltration to the groundwater salinization. However, the results of groundwater Cl/Br molar ratio model indicate that the effect of saline soil flushing practice is limited to account for the observed salinity variation in groundwater. The plots of groundwater Cl vs. Cl/Br molar ratio, and Cl vs δ{sup 37}Cl perform the dominant effects of evapotranspiration on groundwater salinization. Inverse geochemical modeling results show that evapotranspiration may cause approximately 66% loss of shallow groundwater to account for the observed hydrochemical pattern. Due to the redox condition fluctuation induced by irrigation activities and evapotranspiration, groundwater salinization processes have negative effects on groundwater arsenic enrichment. For groundwater iodine and fluoride enrichment, evapotranspiration partly accounts for their elevation in slightly saline water. However, too strong evapotranspiration would restrict groundwater fluoride concentration due to the limitation of fluorite solubility. - Highlights: • Natural high arsenic, fluoride and iodine groundwater co-occur with saline water. �

Cl/Br ratios and chlorine isotope evidences for groundwater salinization and its impact on groundwater arsenic, fluoride and iodine enrichment in the Datong basin, China

International Nuclear Information System (INIS)

Li, Junxia; Wang, Yanxin; Xie, Xianjun

2016-01-01

In order to identify the salinization processes and its impact on arsenic, fluoride and iodine enrichment in groundwater, hydrogeochemical and environmental isotope studies have been conducted on groundwater from the Datong basin, China. The total dissolved solid (TDS) concentrations in groundwater ranged from 451 to 8250 mg/L, and 41% of all samples were identified as moderately saline groundwater with TDS of 3000–10,000 mg/L. The results of groundwater Cl concentrations, Cl/Br molar ratio and Cl isotope composition suggest that three processes including water-rock interaction, surface saline soil flushing, and evapotranspiration result in the groundwater salinization in the study area. The relatively higher Cl/Br molar ratio in groundwater from multiple screening wells indicates the contribution of halite dissolution from saline soil flushed by vertical infiltration to the groundwater salinization. However, the results of groundwater Cl/Br molar ratio model indicate that the effect of saline soil flushing practice is limited to account for the observed salinity variation in groundwater. The plots of groundwater Cl vs. Cl/Br molar ratio, and Cl vs δ"3"7Cl perform the dominant effects of evapotranspiration on groundwater salinization. Inverse geochemical modeling results show that evapotranspiration may cause approximately 66% loss of shallow groundwater to account for the observed hydrochemical pattern. Due to the redox condition fluctuation induced by irrigation activities and evapotranspiration, groundwater salinization processes have negative effects on groundwater arsenic enrichment. For groundwater iodine and fluoride enrichment, evapotranspiration partly accounts for their elevation in slightly saline water. However, too strong evapotranspiration would restrict groundwater fluoride concentration due to the limitation of fluorite solubility. - Highlights: • Natural high arsenic, fluoride and iodine groundwater co-occur with saline water. • Groundwater

Maps of the Bonsall area of the San Luis Rey River valley, San Diego County, California, showing geology, hydrology, and ground-water quality

Science.gov (United States)

Izbicki, John A.

1985-01-01

In November 1984, 84 wells and 1 spring in the Bonsall area of the San Luis Rey River valley were inventoried by U.S. Geological Survey personnel. Depth to water in 38 wells ranged from 1.3 to 38 ft and 23 wells had depths to water less than 10 feet. Dissolved solids concentration of water from 29 wells and 1 spring sampled in autumn 1983 and spring 1984 ranged from 574 to 2,370 mgs/L. Groundwater with a dissolved solids concentration less than 1,000 mgs/L was generally restricted to the eastern part of the aquifer. The total volume of alluvial fill in the Bonsall area is 113,000 acre-feet; the amount of groundwater storage available in the alluvial aquifer is 18,000 acre-feet. The alluvial aquifer is, in part, surrounded and underlain by colluvium and weathered crystalline rock that add some additional groundwater storage capacity to the system. Data in this report are presented on five maps showing well locations , thickness of alluvial fill, water level contours in November 1983 and hydrographs of selected wells, groundwater quality in spring 1960 and graphs showing changes in dissolved solids concentrations of water from selected wells with time, and groundwater quality in spring 1984. This report is part of a larger cooperative project between the Rainbow Municipal Irrigation District and the U.S. Geological Survey. The purpose of the larger project is to develop an appropriate groundwater management plan for the Bonsall area of the San Luis Rey River valley. (USGS)

Water resources and effects of potential surface coal mining on dissolved solids in Hanging Woman Creek basin, southeastern Montana

Science.gov (United States)

Cannon, M.R.

1989-01-01

Groundwater resources of the Hanging Woman Creek basin, Montana include Holocene and Pleistocene alluvial aquifers and sandstone , coal, and clinker aquifers in the Paleocene Fort Union Formation. Surface water resources are composed of Hanging Woman Creek, its tributaries, and small stock ponds. Dissolved-solids concentrations in groundwater ranged from 200 to 11,00 mg/L. Generally, concentrations were largest in alluvial aquifers and smallest in clinker aquifers. Near its mouth, Hanging Woman Creek had a median concentration of about 1,800 mg/L. Mining of the 20-foot to 35-foot-thick Anderson coal bed and 3-foot to 16-foot thick Dietz coal bed could increase dissolved-solids concentrations in shallow aquifers and in Hanging Woman Creek because of leaching of soluble minerals from mine spoils. Analysis of saturated-paste extracts from 158 overburden samples indicated that water moving through mine spoils would have a median increase in dissolved-solids concentration of about 3,700 mg/L, resulting in an additional dissolved-solids load to Hanging Woman Creek of about 3.0 tons/day. Hanging Woman Creek near Birney could have an annual post-mining dissolved-solids load of 3,415 tons at median discharge, a 47% increase from pre-mining conditions load. Post-mining concentrations of dissolved solids, at median discharge, could range from 2,380 mg/L in March to 3,940 mg/L in August, compared to mean pre-mining concentrations that ranged from 1,700 mg/L in July, November, and December to 2,060 mg/L in May. Post-mining concentrations and loads in Hanging Woman Creek would be smaller if a smaller area were mined. (USGS)

Minimum energy requirements for desalination of brackish groundwater in the United States with comparison to international datasets

Science.gov (United States)

Ahdab, Yvana D.; Thiel, Gregory P.; Böhlke, John Karl; Stanton, Jennifer S.; Lienhard, John H.

2018-01-01

This paper uses chemical and physical data from a large 2017 U.S. Geological Surveygroundwater dataset with wells in the U.S. and three smaller international groundwater datasets with wells primarily in Australia and Spain to carry out a comprehensive investigation of brackish groundwater composition in relation to minimum desalinationenergy costs. First, we compute the site-specific least work required for groundwater desalination. Least work of separation represents a baseline for specific energy consumptionof desalination systems. We develop simplified equations based on the U.S. data for least work as a function of water recovery ratio and a proxy variable for composition, either total dissolved solids, specific conductance, molality or ionic strength. We show that the U.S. correlations for total dissolved solids and molality may be applied to the international datasets. We find that total molality can be used to calculate the least work of dilute solutions with very high accuracy. Then, we examine the effects of groundwater solute composition on minimum energy requirements, showing that separation requirements increase from calcium to sodium for cations and from sulfate to bicarbonate to chloride for anions, for any given TDS concentration. We study the geographic distribution of least work, total dissolved solids, and major ions concentration across the U.S. We determine areas with both low least work and high water stress in order to highlight regions holding potential for desalination to decrease the disparity between high water demand and low water supply. Finally, we discuss the implications of the USGS results on water resource planning, by comparing least work to the specific energy consumption of brackish water reverse osmosisplants and showing the scaling propensity of major electrolytes and silica in the U.S. groundwater samples.

Arsenic mineral dissolution and possible mobilization in mineral-microbe-groundwater environment.

Science.gov (United States)

Islam, A B M R; Maity, Jyoti Prakash; Bundschuh, Jochen; Chen, Chien-Yen; Bhowmik, Bejon Kumar; Tazaki, Kazue

2013-11-15

Arsenic (As) is widely distributed in the nature as ores or minerals. It has been attracted much attention for the global public health issue, especially for groundwater As contamination. The aim of this study was to elucidate the characteristics of microbes in groundwater where As-minerals were dissolved. An ex situ experiment was conducted with 7 standard As-minerals in bacteria-free groundwater and stored in experimental vessels for 1 year without supplementary nutrients. The pH (6.7-8.4) and EhS.H.E. (24-548 mV) changed between initial (0 day) and final stages (365 days) of experiment. The dissolution of As was detected higher from arsenolite (4240 ± 8.69 mg/L) and native arsenic (4538 ± 9.02 mg/L), whereas moderately dissolved from orpiment (653 ± 3.56 mg/L) and realgar (319 ± 2.56 mg/L) in compare to arsenopyrite (85 ± 1.25mg/L) and tennantite (3 ± 0.06 mg/L). Optical microscopic, scanning electron microscopic observations and flurometric enumeration revealed the abundance of As-resistant bacillus, coccus and filamentous types of microorganisms on the surface of most of As-mineral. 4'-6-Diamidino-2-phenylindole (DAPI)-stained epifluorescence micrograph confirmed the presence of DNA and carboxyfluorescein diacetate (CFDA) staining method revealed the enzymatically active bacteria on the surface of As-minerals such as in realgar (As4S4). Therefore, the microbes enable to survive and mobilize the As in groundwater by dissolution/bioweathering of As-minerals. Copyright © 2012. Published by Elsevier B.V.

Maintained larval growth in mussel larvae exposed to acidified under-saturated seawater

Science.gov (United States)

Ventura, Alexander; Schulz, Sabrina; Dupont, Sam

2016-03-01

Ocean acidification (OA) is known to affect bivalve early life-stages. We tested responses of blue mussel larvae to a wide range of pH in order to identify their tolerance threshold. Our results confirmed that decreasing seawater pH and decreasing saturation state increases larval mortality rate and the percentage of abnormally developing larvae. Virtually no larvae reared at average pHT 7.16 were able to feed or reach the D-shell stage and their development appeared to be arrested at the trochophore stage. However larvae were capable of reaching the D-shell stage under milder acidification (pHT ≈ 7.35, 7.6, 7.85) including in under-saturated seawater with Ωa as low as 0.54 ± 0.01 (mean ± s. e. m.), with a tipping point for normal development identified at pHT 7.765. Additionally growth rate of normally developing larvae was not affected by lower pHT despite potential increased energy costs associated with compensatory calcification in response to increased shell dissolution. Overall, our results on OA impacts on mussel larvae suggest an average pHT of 7.16 is beyond their physiological tolerance threshold and indicate a shift in energy allocation towards growth in some individuals revealing potential OA resilience.

Temporal variations of methane concentration and isotopic composition in groundwater of the St. Lawrence Lowlands, eastern Canada

Science.gov (United States)

Rivard, Christine; Bordeleau, Geneviève; Lavoie, Denis; Lefebvre, René; Malet, Xavier

2018-03-01

Dissolved methane concentrations in shallow groundwater are known to vary both spatially and temporally. The extent of these variations is poorly documented although this knowledge is critical for distinguishing natural fluctuations from anthropogenic impacts stemming from oil and gas activities. This issue was addressed as part of a groundwater research project aiming to assess the risk of shale gas development for groundwater quality over a 500-km2 area in the St. Lawrence Lowlands (Quebec, Canada). A specific study was carried out to define the natural variability of methane concentrations and carbon and hydrogen isotope ratios in groundwater, as dissolved methane is naturally ubiquitous in aquifers of this area. Monitoring was carried out over a period of up to 2.5 years in seven monitoring wells. Results showed that for a given well, using the same sampling depth and technique, methane concentrations can vary over time from 2.5 to 6 times relative to the lowest recorded value. Methane isotopic composition, which is a useful tool to distinguish gas origin, was found to be stable for most wells, but varied significantly over time in the two wells where methane concentrations are the lowest. The use of concentration ratios, as well as isotopic composition of methane and dissolved inorganic carbon (DIC), helped unravel the processes responsible for these variations. This study indicates that both methane concentrations and isotopic composition, as well as DIC isotopes, should be regularly monitored over at least 1 year to establish their potential natural variations prior to hydrocarbon development.

HANFORD GROUNDWATER REMEDIATION

Energy Technology Data Exchange (ETDEWEB)

CHARBONEAU, B; THOMPSON, M; WILDE, R.; FORD, B.; GERBER, M.S.

2006-02-01

By 1990 nearly 50 years of producing plutonium put approximately 1.70E + 12 liters (450 billion gallons) of liquid wastes into the soil of the 1,518-square kilometer (586-square mile) Hanford Site in southeast Washington State. The liquid releases consisted of chemicals used in laboratory experiments, manufacturing and rinsing uranium fuel, dissolving that fuel after irradiation in Hanford's nuclear reactors, and in liquefying plutonium scraps needed to feed other plutonium-processing operations. Chemicals were also added to the water used to cool Hanford's reactors to prevent corrosion in the reactor tubes. In addition, water and acid rinses were used to clean plutonium deposits from piping in Hanford's large radiochemical facilities. All of these chemicals became contaminated with radionuclides. As Hanford raced to help win World War II, and then raced to produce materials for the Cold War, these radioactive liquid wastes were released to the Site's sandy soils. Early scientific experiments seemed to show that the most highly radioactive components of these liquids would bind to the soil just below the surface of the land, thus posing no threat to groundwater. Other experiments predicted that the water containing most radionuclides would take hundreds of years to seep into groundwater, decaying (or losing) most of its radioactivity before reaching the groundwater or subsequently flowing into the Columbia River, although it was known that some contaminants like tritium would move quickly. Evidence today, however, shows that many contaminants have reached the Site's groundwater and the Columbia River, with more on its way. Over 259 square kilometers (100 square miles) of groundwater at Hanford have contaminant levels above drinking-water standards. Also key to successfully cleaning up the Site is providing information resources and public-involvement opportunities to Hanford's stakeholders. This large, passionate, diverse, and

Sorption of neptunium under oxidizing and reducing groundwater conditions

International Nuclear Information System (INIS)

Hakanen, M.

1991-01-01

Sorption of neptunium was studied under aerobic, anoxic and reducing groundwater conditions using solutions with initial Np concentrations of 10 -14 to 10 -8 mol/l. Under aerobic conditions the sorption was the same for all concentrations. Under anoxic conditions the same proportion of neptunium (70-80%) was removed from the water. The neptunium sorbed on rock surfaces was of mixed oxidation states. Only Np(V) was found in waters. Under reducing groundwater conditions, nearly all the neptunium was removed from water. The sorbed neptunium was at first almost completely in the form of Np(IV). The submicrogram amounts of neptunium were partly oxidized with time, but Np(V) did not dissolve in reducing water. The holding oxidant character of the tonalite to Np(V) and, the holding reductant character of rocks to small amounts of Np(IV), was demonstrated under anaerobic and reducing groundwater conditions, respectively. (orig.)

Geochemistry and isotope hydrology of groundwaters in the Stripa Granite: results and preliminary interpretation

International Nuclear Information System (INIS)

Fritz, P.; Barker, J.F.; Gale, J.E.

1979-04-01

The results of geochemical and isotopic analyses on water samples from the granite at Stripa, Sweden, are presented. Groundwater samples collected from shallow, private wells; surface boreholes; and boreholes drilled from the 330 m and 410 m mine levels were analyzed for their major ion chemistry, dissolved gases, and environmental isotope contents. The principal change in the chemical load with depth is typified by chloride concentration, which increases from less than 5 mg/liter to about 300 mg/liter. There is a parallel increase in pH, which changes from about 6.5 to over 9.75. It is important to notice that calcite saturation is maintained and that, because of rising pH, dissolved inorganic carbon is lost. The total carbonate content thus decreases from about 70 mg/liter to less than 7 mg/liter. The 18 O and deuterium analyses demonstrate that different fracture systems contain different water masses, whose age increases with depth. Groundwater age determinations with 14 C and isotopes of the uranium decay series strongly indicate that water ages exceed 25,000 years. The 13 C contents of the aqueous carbonate in these groundwaters indicate groundwater recharge through vegetated soil, presumably during an interglacial period. The 13 C and 18 O determinations show that most fracture calcites have formed in a wide variety of depositional environments, and not in the waters circulating today

Lead pollution of soil and groundwater in clay-pigeon shooting ranges

International Nuclear Information System (INIS)

Hahn, R.

1990-01-01

Within the framework of the exemplary investigation of soil and groundwater pollution with lead on clay-pigeon shooting ranges, three facilities were sampled. The analyses for depth distribution in the main area of the ammunition deposition showed that the dissolved lead amounts are as a rule smaller than the limiting value of the Sewage Sludge Regulation (100 mg/kg). In two groundwater samples, no lead could be found. Considerable amounts of small lead balls are found on the soil surface, but only a very small part appears to be washed out and adsorbed by the soil matrix. (orig.) [de

Long-term natural attenuation of carbon and nitrogen within a groundwater plume after removal of the treated wastewater source.

Science.gov (United States)

Repert, Deborah A; Barber, Larry B; Hess, Kathryn M; Keefe, Steffanie H; Kent, Douglas B; LeBlanc, Denis R; Smith, Richard L

2006-02-15

Disposal of treated wastewater for more than 60 years onto infiltration beds on Cape Cod, Massachusetts produced a groundwater contaminant plume greater than 6 km long in a surficial sand and gravel aquifer. In December 1995 the wastewater disposal ceased. A long-term, continuous study was conducted to characterize the post-cessation attenuation of the plume from the source to 0.6 km downgradient. Concentrations and total pools of mobile constituents, such as boron and nitrate, steadily decreased within 1-4 years along the transect. Dissolved organic carbon loads also decreased, but to a lesser extent, particularly downgradient of the infiltration beds. After 4 years, concentrations and pools of carbon and nitrogen in groundwater were relatively constant with time and distance, but substantially elevated above background. The contaminant plume core remained anoxic for the entire 10-year study period; temporal patterns of integrated oxygen deficit decreased slowly at all sites. In 2004, substantial amounts of total dissolved carbon (7 mol C m(-2)) and fixed (dissolved plus sorbed) inorganic nitrogen (0.5 mol N m(-2)) were still present in a 28-m vertical interval at the disposal site. Sorbed constituents have contributed substantially to the dissolved carbon and nitrogen pools and are responsible for the long-term persistence of the contaminant plume. Natural aquifer restoration at the discharge location will take at least several decades, even though groundwater flow rates and the potential for contaminant flushing are relatively high.

Considerations in modeling groundwater inflow to underground respositories

International Nuclear Information System (INIS)

Freeze, G.; Christian-Frear, T.

1996-01-01

Groundwater in and around underground radioactive waste repositories has several potential effects on repository performance. Repository excavation produces conditions where the repository is underpressured relative to the surrounding host rock, resulting in groundwater inflow to the repository. The presence of groundwater has been shown to enhance gas generation from emplaced waste forms, which expedites repository pressurization. Repository pressurization results in an increased driving force for dissolved radionuclide movement away from the repository. Repository excavation also produces a zone surrounding the repository having disturbed hydrologic and geochemical properties. Within the disturbed rock zone (DRZ), intrinsic permeability and porosity change over time due to the formation of microfractures and grain boundary dilation. Additionally, elastic and inelastic changes in pore volume may cause variation in the near-field fluid pressure and fluid saturation distributions that influence groundwater flow toward the repository excavation. Increased permeability, decreased pore-fluid pressure, and partially saturated conditions in the DRZ contribute to enhancing potential release pathways away from the repository. It is important for a repository performance assessment to consider chemical processes, hydrologic processes, as well as the complex coupling between these processes

Groundwater and underground coal gasification in Alberta

International Nuclear Information System (INIS)

Haluszka, A.; MacMillan, G.; Maev, S.

2010-01-01

Underground coal gasification has potential in Alberta. This presentation provided background information on underground coal gasification and discussed groundwater and the Laurus Energy demonstration project. A multi-disciplined approach to project assessment was described with particular reference to geologic and hydrogeologic setting; geologic mapping; and a hydrogeologic numerical model. Underground coal gasification involves the conversion of coal into synthesis gas or syngas. It can be applied to mined coal at the surface or applied to non-mined coal seams using injection and production wells. Underground coal gasification can effect groundwater as the rate of water influx into the coal seams influences the quality and composition of the syngas. Byproducts created include heat as well as water with dissolved concentrations of ammonia, phenols, salts, polyaromatic hydrocarbons, and liquid organic products from the pyrolysis of coal. A process overview of underground coal gasification was also illustrated. It was concluded that underground coal gasification has the potential in Alberta and risks to groundwater could be minimized by a properly designed project. refs., figs.

Hydrochemistry and Isotope Hydrology for Groundwater Sustainability of the Coastal Multilayered Aquifer System (Zhanjiang, China

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Pengpeng Zhou

2017-01-01

Full Text Available Groundwater sustainability has become a critical issue for Zhanjiang (China because of serious groundwater level drawdown induced by overexploitation of its coastal multilayered aquifer system. It is necessary to understand the origins, material sources, hydrochemical processes, and dynamics of the coastal groundwater in Zhanjiang to support its sustainable management. To this end, an integrated analysis of hydrochemical and isotopic data of 95 groundwater samples was conducted. Hydrochemical analysis shows that coastal groundwater is fresh; however, relatively high levels of Cl−, Mg2+, and total dissolved solid (TDS imply slight seawater mixing with coastal unconfined groundwater. Stable isotopes (δ18O and δ2H values reveal the recharge sources of groundwater in the multilayered aquifer system. The unconfined groundwater originates from local modern precipitation; the confined groundwater in mainland originates from modern precipitation in northwestern mountain area, and the confined groundwater in Donghai and Leizhou is sourced from rainfall recharge during an older period with a colder climate. Ionic relations demonstrate that silicate weathering, carbonate dissolutions, and cation exchange are the primary processes controlling the groundwater chemical composition. Declining trends of groundwater level and increasing trends of TDS of the confined groundwater in islands reveal the landward extending tendency of the freshwater-seawater mixing zone.

The variation of calcium, magnesium, sodium, potassium and bicarbonate concentration, pH and conductivity in groundwater of Karachi region

International Nuclear Information System (INIS)

Zubair, A.; Ali, S.I.

2002-01-01

Groundwater in Karachi is influenced mainly by the evaporation / crystallization process as expressed by the Na/(Na+Ca) weight concentration ratio. The high coefficient of determined between conductivity and total dissolved ions concentration in meq/sup -1/ revealed that major ions affect the conductivity of groundwater. It was also found that groundwater quality with respect to cations is not significantly influenced by geology, particularly in the Urban are of the city, where the 90% of the population resides. The relationship between conductivity and bicarbonate concentration shows that supersaturation of groundwater with carbon dioxide is responsible for general depression of pH. (author)

Installation of a groundwater monitoring-well network on the east side of the Uncompahgre River in the Lower Gunnison River Basin, Colorado, 2014

Science.gov (United States)

Thomas, Judith C.

2015-10-07

The east side of the Uncompahgre River Basin has been a known contributor of dissolved selenium to recipient streams. Discharge of groundwater containing dissolved selenium contributes to surface-water selenium concentrations and loads; however, the groundwater system on the east side of the Uncompahgre River Basin is not well characterized. The U.S. Geological Survey, in cooperation with the Colorado Water Conservation Board and the Bureau of Reclamation, has established a groundwater-monitoring network on the east side of the Uncompahgre River Basin. Thirty wells total were installed for this project: 10 in 2012 (DS 923, http://dx.doi.org/10.3133/ds923), and 20 monitoring wells were installed during April and June 2014 which are presented in this report. This report presents location data, lithologic logs, well-construction diagrams, and well-development information. Understanding the groundwater system can provide managers with an additional metric for evaluating the effectiveness of salinity and selenium control projects.

Source partitioning of anthropogenic groundwater nitrogen in a mixed-use landscape, Tutuila, American Samoa

Science.gov (United States)

Shuler, Christopher K.; El-Kadi, Aly I.; Dulai, Henrietta; Glenn, Craig R.; Fackrell, Joseph

2017-12-01

This study presents a modeling framework for quantifying human impacts and for partitioning the sources of contamination related to water quality in the mixed-use landscape of a small tropical volcanic island. On Tutuila, the main island of American Samoa, production wells in the most populated region (the Tafuna-Leone Plain) produce most of the island's drinking water. However, much of this water has been deemed unsafe to drink since 2009. Tutuila has three predominant anthropogenic non-point-groundwater-pollution sources of concern: on-site disposal systems (OSDS), agricultural chemicals, and pig manure. These sources are broadly distributed throughout the landscape and are located near many drinking-water wells. Water quality analyses show a link between elevated levels of total dissolved groundwater nitrogen (TN) and areas with high non-point-source pollution density, suggesting that TN can be used as a tracer of groundwater contamination from these sources. The modeling framework used in this study integrates land-use information, hydrological data, and water quality analyses with nitrogen loading and transport models. The approach utilizes a numerical groundwater flow model, a nitrogen-loading model, and a multi-species contaminant transport model. Nitrogen from each source is modeled as an independent component in order to trace the impact from individual land-use activities. Model results are calibrated and validated with dissolved groundwater TN concentrations and inorganic δ15N values, respectively. Results indicate that OSDS contribute significantly more TN to Tutuila's aquifers than other sources, and thus should be prioritized in future water-quality management efforts.

Groundwater Pollution Sources Apportionment in the Ghaen Plain, Iran

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Mohammad Reza Vesali Naseh

2018-01-01

Full Text Available Although Iran’s Ghaen Plain provides saffron to much of the world, no regional groundwater quality (GQ assessment has yet been undertaken. Given the region’s potential for saltwater intrusion and heavy metal contamination, it is important to assess the GQ and determine its main probable source of pollution (MPSP. Such knowledge would allow for informed mitigation or elimination of the potential adverse health effects of this groundwater through its use as drinking water, or indirectly as a result of the consumption of groundwater-irrigated crops. Total dissolved solids, sodium, and chloride in the water of the majority of 16 wells sampled within the region exceeded World Health Organization and Iranian permissible standards for drinking water. The groundwater proved to only be suitable for irrigating salt tolerant crops under good drainage conditions. Due to the precipitation of calcium carbonate in the water supply facilities, the water from all wells was deemed unsuitable for industrial purposes. Heavy metal pollution and contamination indices showed no groundwater contamination. Analysis of ionic ratios and the application of principal components analysis indicated the MPSP to be saltwater intrusion, with the geology subtending the plain, and to a lesser extent, anthropogenic activities. Reducing groundwater withdrawals, particularly those for agricultural production by using high performance irrigation methods could reduce saltwater intrusion and improve GQ in the Ghaen Plain.

Groundwater Pollution Sources Apportionment in the Ghaen Plain, Iran.

Science.gov (United States)

Vesali Naseh, Mohammad Reza; Noori, Roohollah; Berndtsson, Ronny; Adamowski, Jan; Sadatipour, Elaheh

2018-01-22

Although Iran's Ghaen Plain provides saffron to much of the world, no regional groundwater quality (GQ) assessment has yet been undertaken. Given the region's potential for saltwater intrusion and heavy metal contamination, it is important to assess the GQ and determine its main probable source of pollution (MPSP). Such knowledge would allow for informed mitigation or elimination of the potential adverse health effects of this groundwater through its use as drinking water, or indirectly as a result of the consumption of groundwater-irrigated crops. Total dissolved solids, sodium, and chloride in the water of the majority of 16 wells sampled within the region exceeded World Health Organization and Iranian permissible standards for drinking water. The groundwater proved to only be suitable for irrigating salt tolerant crops under good drainage conditions. Due to the precipitation of calcium carbonate in the water supply facilities, the water from all wells was deemed unsuitable for industrial purposes. Heavy metal pollution and contamination indices showed no groundwater contamination. Analysis of ionic ratios and the application of principal components analysis indicated the MPSP to be saltwater intrusion, with the geology subtending the plain, and to a lesser extent, anthropogenic activities. Reducing groundwater withdrawals, particularly those for agricultural production by using high performance irrigation methods could reduce saltwater intrusion and improve GQ in the Ghaen Plain.

Groundwater quality and its suitability for drinking and irrigational use in the Southern Tiruchirappalli district, Tamil Nadu, India

Science.gov (United States)

Selvakumar, S.; Ramkumar, K.; Chandrasekar, N.; Magesh, N. S.; Kaliraj, S.

2017-03-01

A total of 20 groundwater samples were collected from both dug and bore wells of southern Tiruchirappalli district and analyzed for various hydrogeochemical parameters. The analyzed physicochemical parameters such as pH, electrical conductivity, total dissolved solids, calcium, magnesium, sodium, potassium, bicarbonate, carbonate, sulfate, chloride, nitrate, and fluoride are used to characterize the groundwater quality and its suitability for drinking and irrigational uses. The results of the chemical analysis indicates that the groundwater in the study area is slightly alkaline and mainly contains Na+, Ca2+, and Mg2+ cations as well as HCO3 2-, Cl-, SO4 2-and NO3 - anions. The total dissolved solids mainly depend on the concentration of major ions such as Ca, Mg, Na, K, HCO3, Cl, and SO4. Based on TDS, 55 % of the samples are suitable for drinking and rest of the samples are unsuitable for drinking. The total hardness indicates that majority of the groundwater samples are found within the permissible limit of WHO. The dominant hydrochemical facies for groundwater are Ca-Mg-Cl, Ca-HCO3, and Ca-Cl type. The USSL graphical geochemical representation of groundwater quality suggests that majority of the water samples belongs to high medium salinity with low alkali hazards. The Gibb's plot indicates that the groundwater chemistry of the study area is mainly controlled by evaporation and rock-water interaction. Spearman's correlation and factor analysis were used to distinguish the statistical relation between different ions and contamination source in the study area.

Dissolved Organic Matter (DOM) Export from Watersheds to Coastal Oceans

Science.gov (United States)

Chen, R. F.; Gardner, G. B.; Peri, F.

2016-02-01

Dissolved organic matter (DOM) from terrestrial plants and soils is transported by surface waters and groundwaters to coastal ocean waters. Along the way, photochemical and biological degradation can remove DOM, and in situ processes such as phytoplankton leaching and sediment sources can add to the DOM in the river water. Wetlands, especially coastal wetlands can add significant amounts of DOM that is carried by rivers and is exported through estuaries to coastal systems. We will present observational data from a variety of coastal systems (San Francisco Bay, Boston Harbor, Chesapeake Bay, Hudson River, the Mississippi River, and a small salt marsh in the Gulf of Mexico). High resolution measurements of chromophoric dissolved organic matter (CDOM) can be correlated with dissolved organic carbon (DOC) so can be used to estimate DOC in specific systems and seasons. Gradients in CDOM/DOC combined with water fluxes can be used to estimate DOC fluxes from a variety of coastal watersheds to coastal systems. Influences of land use, system size, residence time, DOM quality, and photochemical and biological degradation will be discussed. The significance of coastal wetlands in the land-to-ocean export of DOC will be emphasized.

Effects of stormwater infiltration on quality of groundwater beneath retention and detention basins

Science.gov (United States)

Fischer, D.; Charles, E.G.; Baehr, A.L.

2003-01-01

Infiltration of storm water through detention and retention basins may increase the risk of groundwater contamination, especially in areas where the soil is sandy and the water table shallow, and contaminants may not have a chance to degrade or sorb onto soil particles before reaching the saturated zone. Groundwater from 16 monitoring wells installed in basins in southern New Jersey was compared to the quality of shallow groundwater from 30 wells in areas of new-urban land use. Basin groundwater contained much lower levels of dissolved oxygen, which affected concentrations of major ions. Patterns of volatile organic compound and pesticide occurrence in basin groundwater reflected the land use in the drainage areas served by the basins, and differed from patterns in background samples, exhibiting a greater occurrence of petroleum hydrocarbons and certain pesticides. Dilution effects and volatilization likely decrease the concentration and detection frequency of certain compounds commonly found in background groundwater. High recharge rates in storm water basins may cause loading factors to be substantial even when constituent concentrations in infiltrating storm water are relatively low.

Groundwater-level trends and forecasts, and salinity trends, in the Azraq, Dead Sea, Hammad, Jordan Side Valleys, Yarmouk, and Zarqa groundwater basins, Jordan

Science.gov (United States)

Goode, Daniel J.; Senior, Lisa A.; Subah, Ali; Jaber, Ayman

2013-01-01

Changes in groundwater levels and salinity in six groundwater basins in Jordan were characterized by using linear trends fit to well-monitoring data collected from 1960 to early 2011. On the basis of data for 117 wells, groundwater levels in the six basins were declining, on average about -1 meter per year (m/yr), in 2010. The highest average rate of decline, -1.9 m/yr, occurred in the Jordan Side Valleys basin, and on average no decline occurred in the Hammad basin. The highest rate of decline for an individual well was -9 m/yr. Aquifer saturated thickness, a measure of water storage, was forecast for year 2030 by using linear extrapolation of the groundwater-level trend in 2010. From 30 to 40 percent of the saturated thickness, on average, was forecast to be depleted by 2030. Five percent of the wells evaluated were forecast to have zero saturated thickness by 2030. Electrical conductivity was used as a surrogate for salinity (total dissolved solids). Salinity trends in groundwater were much more variable and less linear than groundwater-level trends. The long-term linear salinity trend at most of the 205 wells evaluated was not increasing, although salinity trends are increasing in some areas. The salinity in about 58 percent of the wells in the Amman-Zarqa basin was substantially increasing, and the salinity in Hammad basin showed a long-term increasing trend. Salinity increases were not always observed in areas with groundwater-level declines. The highest rates of salinity increase were observed in regional discharge areas near groundwater pumping centers.

Tracer attenuation in groundwater

Science.gov (United States)

Cvetkovic, Vladimir

2011-12-01

The self-purifying capacity of aquifers strongly depends on the attenuation of waterborne contaminants, i.e., irreversible loss of contaminant mass on a given scale as a result of coupled transport and transformation processes. A general formulation of tracer attenuation in groundwater is presented. Basic sensitivities of attenuation to macrodispersion and retention are illustrated for a few typical retention mechanisms. Tracer recovery is suggested as an experimental proxy for attenuation. Unique experimental data of tracer recovery in crystalline rock compare favorably with the theoretical model that is based on diffusion-controlled retention. Non-Fickian hydrodynamic transport has potentially a large impact on field-scale attenuation of dissolved contaminants.

Arsenic, manganese and aluminum contamination in groundwater resources of Western Amazonia (Peru).

Science.gov (United States)

de Meyer, Caroline M C; Rodríguez, Juan M; Carpio, Edward A; García, Pilar A; Stengel, Caroline; Berg, Michael

2017-12-31

This paper presents a first integrated survey on the occurrence and distribution of geogenic contaminants in groundwater resources of Western Amazonia in Peru. An increasing number of groundwater wells have been constructed for drinking water purposes in the last decades; however, the chemical quality of the groundwater resources in the Amazon region is poorly studied. We collected groundwater from the regions of Iquitos and Pucallpa to analyze the hydrochemical characteristics, including trace elements. The source aquifer of each well was determined by interpretation of the available geological information, which identified four different aquifer types with distinct hydrochemical properties. The majority of the wells in two of the aquifer types tap groundwater enriched in aluminum, arsenic, or manganese at levels harmful to human health. Holocene alluvial aquifers along the main Amazon tributaries with anoxic, near pH-neutral groundwater contained high concentrations of arsenic (up to 700μg/L) and manganese (up to 4mg/L). Around Iquitos, the acidic groundwater (4.2≤pH≤5.5) from unconfined aquifers composed of pure sand had dissolved aluminum concentrations of up to 3.3mg/L. Groundwater from older or deeper aquifers generally was of good chemical quality. The high concentrations of toxic elements highlight the urgent need to assess the groundwater quality throughout Western Amazonia. Copyright © 2017 Elsevier B.V. All rights reserved.

Discharge of 210Po and 210Pb in coastal groundwater to the ocean

International Nuclear Information System (INIS)

Kim, Intae; Kim, Tae-hoon; Kim, Guebuem

2013-01-01

The activities of 210 Po and 210 Pb were measured for the truly dissolved (<10 kDa) and colloidal (10 kDa - 0.45 ìm) phases in coastal ground water in 2010 and 2011. The sampling sites include the coast of a large tidal flat (Hampyeong Bay) and a volcanic island, Jeju, Korea, where submarine groundwater discharge (SGD) were reported to be higher than typical continental margins. The total dissolved fraction was separated into the colloidal and truly dissolved fractions using a tangential flow filtration (TFF) system (PLCGC Pellicon). The total 210 Po and 210 Pb activities in ground water were 1.0 - 18.2 dpm/100L (9.7±7.6 dpm/100L) an 2.9 - 29.1 dpm/100L (16.8±10.7 dpm/100L) in the Hampyeong Bay and Jeju Island samples, respectively. The total 210 Po and 210 Pb activities in groundwater were similar to or even slightly lower than those in the typical seawater. These lower activities seem to be due to the rapid adsorption of Po and Pb on to particles in the subterranean estuary. The proportions of the truly dissolved and colloidal phases were, respectively, 73±5% and 27±5% for 210 Po, and 60±5% and 40±5% for 210 Pb. This result is consistent with the earlier study that more than half of the some dissolved trace metals in coastal ground water are in the colloidal form. Thus, our result implies that the colloidal forms are important in controlling the behaviour of Po, Pb, and other trace metals in the subterranean estuary and SGD-associated fluxes to the ocean. (author)

Initial studies of submarine groundwater discharge in Mississippi coastal waters

Science.gov (United States)

Shiller, A. M.; Moore, W. S.; Joung, D. J.; Box, H.; Ho, P.; Whitmore, L. M.; Gilbert, M.; Anderson, H.

2017-12-01

Submarine groundwater discharge (SGD) is a critical component of coastal ecosystems, affecting biogeochemistry and productivity. The SGD flux and effect on the ecosystem of the Mississippi (MS) Bight has not previously been studied. We have determined Ba, δ18O of water, and Ra-isotopes, together with nutrients, chlorophyll, and dissolved oxygen (DO) during multiple cruises from fall 2015 to summer 2016. Water isotope distributions (δ18O) show that, although the MS River Delta bounds the western side of the Bight, nonetheless, Mobile Bay and other local rivers are the Bight's dominant freshwater sources. But elevated dissolved Ba and Ra isotopes cannot be explained by river input. Spatially, SGD in the MS Bight occurs over a wide area, with hot spots near the barrier islands (e.g., Chandeleurs, Horn and Dauphin Islands) and the mouth of Mobile Bay, probably in association with old buried river channels, or dredged ship channels. Based on their high concentrations in saline groundwaters sampled on the barrier islands, the elevated Ba and Ra in MS Bight water are likely due to SGD. In subsurface waters, long-lived Ra isotopes were negatively correlated with DO during spring and summer 2016, suggesting direct discharge of DO-depleted groundwater and/or accumulation of SGD-derived Ra and microbial DO consumption under strongly stratified conditions. Our ongoing study suggests that seasonal variability in flushing, water stratification, and SGD input play important roles in biological production and bottom water hypoxia in the MS Bight.

Interaction between surface water areas and groundwater in Hanoi city, Viet Nam

Science.gov (United States)

Hayashi, T.; Kuroda, K.; Do Thuan, A.; Tran Thi Viet, N.; Takizawa, S.

2012-12-01

Hanoi is the capital of Viet Nam and the second largest city in this country (population: 6.45 million in 2009). Hanoi city has developed along the Red River and has many lakes, ponds and canals. However, recent rapid urbanization of this city has reduced number of natural water areas such as ponds and lakes by reclamation not only in the central area but the suburban area. Canals also have been reclaimed or cut into pieces. Contrary, number of artificial water areas such as fish cultivation pond has rapidly increased. On the other hand, various kind of waste water flows into these natural and artificial water areas and induces pollution and eutrophication. These waste waters also have possibility of pollution of groundwater that is one of major water resources in this city. In addition, groundwater in this area has high concentrations of Arsenic, Fe and NH4. Thus, groundwater use may causes re-circulation of Arsenic. However, studies on the interaction between surface water areas and groundwater and on the role of surface water areas for solute transport with water cycle are a few. Therefore, we focused on these points and took water samples of river, pond and groundwater from four communities in suburban areas: two communities are located near the Red River and other two are far from the River. Also, columnar sediment samples of these ponds were taken and pore water was abstracted. Major dissolved ions, metals and stable isotopes of oxygen and hydrogen of water samples were analyzed. As for water cycle, from the correlation between δ18O and δD, the Red River water (after GNIR) were distributed along the LMWL (δD=8.2δ18O+14.1, calculated from precipitation (after GNIP)). On the other hand, although the pond waters in rainy season were distributed along the LMWL, that in dry season were distributed along the local evaporation line (LEL, slope=5.6). The LEL crossed with the LMWL at around the point of weighted mean values of precipitation in rainy season and of

The Lavia testborehole - a summary of the groundwater investigations in 1984-1985

International Nuclear Information System (INIS)

Wickstroem, P.; Lampen, P.

1986-06-01

In the spring of 1984, a 1001 m deep test borehole with a diameter of 56 mm was core-drilled in a granitic intrusion in Lavia in southwestern Finland. The drilling fluid which was taken from the borehole well was labelled with a stable tracer, i.e. an iodine. Gas-lift pumping by nitrogen gas was carried out after the drilling 1984 and in the spring 1985. The groundwater samples were taken with the equipment developed for deep boreholes. The equipment comprises straddle paker system with a membrane pump and a flow-through-cell system with electrodes. Specific conductivity, amount of dissolved oxygen, pS, pH, temperature and redox-potential of the groundwater samples were measured in this system. Sampling prosedure and data acquisition will be controlled by a microcomputer. The groundwater samples were taken four times at different depths during 1984 - 1985. Sampling was made from 5.4 metre packer-isolated zones from the depths 94 - 99 m, 119 - 124 m, 422 - 427 m, 547 - 552 m, 905 - 910 m and 965 - 970 m. At the depth of 9971 - 1001 m only a single packer was used. The consentration of iodine was frequently controlled during the sampling. Groundwater samples were taken for different physico-chemical analyses. Also samples for isotope and noble gas analyses were taken. The iodine analyses gave the evidence that varying amounts of drilling fluid remain in the bedrock. The analyses manifest that the groundwater of the test borehole has quite a low ionic strength. The measurements of the redox-potential and the amount of dissolved oxygen indicate that reducing conditions seem to exist at the depths of 422 - 427 m and 905 - 910 m. A percussion borehole was drilled near the test borehole without using any drilling fluid. Water samples that had not been contaminated by drilling fluid were taken once. (author)

Hydrogeological, petrophysical and hydrogeochemical characteristics of the groundwater aquifers east of Wadi El-Natrun, Egypt

Directory of Open Access Journals (Sweden)

Zenhom E. Salem

2016-06-01

The concentrations of TDS and the dissolved elements are higher in the shallow groundwater compared to the deeper one, which could be related to soil salinity and evaporation processes. Ion exchange, water–rock interaction and evaporation processes are the main geochemical processes affecting the chemistry of the studied groundwater. Sodium chloride/bicarbonate types are the most common chemical types in the study area. Most of the water samples are of old meteoric origin (Na2SO4 type and old marine origin (MgCl2 type. On the basis of SAR and EC values it is concluded that most of the groundwater samples are suitable for irrigation purposes.

Hydrochemical and multivariate analysis of groundwater quality in the northwest of Sinai, Egypt.

Science.gov (United States)

El-Shahat, M F; Sadek, M A; Salem, W M; Embaby, A A; Mohamed, F A

2017-08-01

The northwestern coast of Sinai is home to many economic activities and development programs, thus evaluation of the potentiality and vulnerability of water resources is important. The present work has been conducted on the groundwater resources of this area for describing the major features of groundwater quality and the principal factors that control salinity evolution. The major ionic content of 39 groundwater samples collected from the Quaternary aquifer shows high coefficients of variation reflecting asymmetry of aquifer recharge. The groundwater samples have been classified into four clusters (using hierarchical cluster analysis), these match the variety of total dissolvable solids, water types and ionic orders. The principal component analysis combined the ionic parameters of the studied groundwater samples into two principal components. The first represents about 56% of the whole sample variance reflecting a salinization due to evaporation, leaching, dissolution of marine salts and/or seawater intrusion. The second represents about 15.8% reflecting dilution with rain water and the El-Salam Canal. Most groundwater samples were not suitable for human consumption and about 41% are suitable for irrigation. However, all groundwater samples are suitable for cattle, about 69% and 15% are suitable for horses and poultry, respectively.

Importance of Rocks and Their Weathering Products on Groundwater Quality in Central-East Cameroon

Directory of Open Access Journals (Sweden)

Merlin Gountié Dedzo

2017-04-01

Full Text Available The present work highlights the influence of lithology on water quality in Méiganga and its surroundings. The main geological formations in this region include gneiss, granite and amphibolite. The soils developed on these rocks are of ABC type, which are acidic to slightly acidic. Electrical conductivity (EC, organic matter, total nitrogen, nitrate-nitrogen, sulfate, chloride, phosphorus and exchangeable base values were low to very low in the soil samples. Groundwater samples were investigated for their physicochemical characteristics. The wide ranges of EC values (15.1–436 µS/cm and total dissolved solids (9–249 mg/L revealed the heterogeneous distribution of hydrochemical processes within the groundwater of the area. The relative abundance of major dissolved species (mg/L was Ca2+ > Na+ > Mg2+ > K+ for cations and HCO3− >> NO3− > Cl− > SO42− for anions. All the groundwater samples were soft, with total hardness values (2.54–136.65 mg/L below the maximum permissible limits of the World Health Organization (WHO guideline. The majority of water samples (67% were classified as mixed CaMg-HCO3 type. Alkaline earth metal contents dominated those of alkali metals in 66.66% of samples. Thus, for the studied groundwater, Mg2+ and Ca2+ ion adsorption by clay minerals was almost nonexistent; this implies their release into the solution, which accounts for their high concentrations compared to alkali metals. Ion geochemistry revealed that water-rock interactions (silicate weathering and ion exchange processes regulated the groundwater chemistry. One water sample points towards the evaporation domain of this diagram, indicating that groundwater probably does not originate from a deeper system. Kaolinite is the most stable secondary phase in the waters in the study area, in accordance with the geochemical process of monosiallitization, which predominated in the humid tropical zone.

Field Evidence for Co-Metabolism of Trichloroethene Stimulated by Addition of Electron Donor to Groundwater

Energy Technology Data Exchange (ETDEWEB)

Conrad, Mark E.; Brodie, Eoin L.; Radtke, Corey W.; Bill, Markus; Delwiche, Mark E.; Lee, M. Hope; Swift, Dana L.; Colwell, Frederick S.

2010-05-17

For more than 10 years, electron donor has been injected into the Snake River aquifer beneath the Test Area North site of the Idaho National Laboratory for the purpose of stimulating microbial reductive dechlorination of trichloroethene (TCE) in groundwater. This has resulted in significant TCE removal from the source area of the contaminant plume and elevated dissolved CH4 in the groundwater extending 250 m from the injection well. The delta13C of the CH4 increases from 56o/oo in the source area to -13 o/oo with distance from the injection well, whereas the delta13C of dissolved inorganic carbon decreases from 8 o/oo to -13 o/oo, indicating a shift from methanogenesis to methane oxidation. This change in microbial activity along the plume axis is confirmed by PhyloChip microarray analyses of 16S rRNA genes obtained from groundwater microbial communities, which indicate decreasing abundances of reductive dechlorinating microorganisms (e.g., Dehalococcoides ethenogenes) and increasing CH4-oxidizing microorganisms capable of aerobic co-metabolism of TCE (e.g., Methylosinus trichosporium). Incubation experiments with 13C-labeled TCE introduced into microcosms containing basalt and groundwater from the aquifer confirm that TCE co-metabolism is possible. The results of these studies indicate that electron donor amendment designed to stimulate reductive dechlorination of TCE may also stimulate co-metabolism of TCE.

Fe(II) oxidation kinetics and Fe hydroxyphosphate precipitation upon aeration of anaerobic (ground)water

NARCIS (Netherlands)

van der Grift, B.; Griffioen, J.; Behrends, T.; Wassen, M.J.; Schot, P.P.; Osté, Leonard

2015-01-01

Exfiltration of anaerobic Fe-rich groundwater into surface water plays an important role in controlling the transport of phosphate (P) from agricultural areas to the sea. Previous laboratory and field studies showed that Fe(II) oxidation upon aeration leads to effective immobilization of dissolved P

A new device for continuous monitoring the CO2 dissolved in water

Science.gov (United States)

de Gregorio, S.; Camarda, M.; Cappuzzo, S.; Giudice, G.; Gurrieri, S.; Longo, M.

2009-04-01

The measurements of dissolved CO2 in water are common elements of industrial processes and scientific research. In order to perform gas dissolved measurements is required to separate the dissolved gaseous phase from water. We developed a new device able to separate the gases phase directly in situ and well suitable for continuous measuring the CO2 dissolved in water. The device is made by a probe of a polytetrafluorethylene (PTFE) tube connected to an I.R. spectrophotometer (I.R.) and a pump. The PTFE is a polymeric semi-permeable membrane and allows the permeation of gas in the system. Hence, this part of the device is dipped in water in order to equilibrate the probe headspace with the dissolved gases. The partial pressure of the gas i in the headspace at equilibrium (Pi) follows the Henry's law: Pi=Hi•Ci, where Hi is the Henry's constant and Ci is the dissolved concentration of gas i. After the equilibrium is achieved, the partial pressure of CO2 inside the tube is equal to the partial pressure of dissolved CO2. The concentration of CO2 is measured by the I.R. connected to the tube. The gas is moved from the tube headspace to the I.R. by using the pump. In order to test the device and assess the best operating condition, several experimental were performed in laboratory. All the test were executed in a special apparatus where was feasible to create controlled atmospheres. Afterward the device has been placed in a draining tunnel sited in the Mt. Etna Volcano edifice (Italy). The monitored groundwater intercepts the Pernicana Fault, along which degassing phenomena are often observed. The values recorded by the station result in agreement with monthly directly measurements of dissolved CO2 partial pressure.

Groundwater sampling from shallow boreholes (PP and PR) and groundwater observation tubes (PVP) at Olkiluoto in 2004

Energy Technology Data Exchange (ETDEWEB)

Hirvonen, H. [Teollisuuden Voima Oyj, Eurajoki (Finland)

2005-11-15

Groundwater sampling from the shallow boreholes and groundwater observation tubes was performed in summer 2004 (PP2, PP3, PP7, PP8, PRl, PVPl, PVP3A, PVP3B, PVP4A and PVP4B) and in autumn 2004 (PP2, PP3, PP5, PP7, PP8, PP9, PP36, PP37, PP39, PR1, PR2, PVP1, PVP3A, PVP3B, PVP4A, PVP8A, PVP9A, PVP9B, PVP10B, PVP11, PVP12, PVP13, PVP14 and PVP20). The results from previous samplings have been used in the hydrogeochemical baseline characterization at Olkiluoto and some of the latest results have also been part of the ONKALO monitoring program. This study contains data on preliminary pumping of the sampling points and pumping for groundwater sampling and chemical analyses in the laboratory. This study also includes comparison with analytical results obtained between 1995-2004. The total dissolved solids (TDS) of groundwater samples were mainly below 1000 mg/L. According to Davis's TDS classification, these waters were fresh waters. The only exception was the water sample from shallow borehole PP7 (1400mg/L and 1450mg/L), which was brackish. Several different groundwater types were observed, but the most common water type was Ca-HCO{sub 3} (five samples). Analytical results from 1995-2003 were compared. During 2001-2003 in groundwater samples from sampling points PVP1, PVP9A and PP7 all measured main parameters changed considerably, but from summer 2003 to autumn 2004 the greatest alterations occurred in PR2, PVP1, PVP3A and PVP3B waters. These changes can be seen in almost all parameters. For other samples only minor changes in results were observed during the reference period. (orig.)

Dissolved radon and uranium in groundwater in a potential coal seam gas development region (Richmond River Catchment, Australia).

Science.gov (United States)

Atkins, Marnie L; Santos, Isaac R; Perkins, Anita; Maher, Damien T

2016-04-01

The extraction of unconventional gas resources such as shale and coal seam gas (CSG) is rapidly expanding globally and often prevents the opportunity for comprehensive baseline groundwater investigations prior to drilling. Unconventional gas extraction often targets geological layers with high naturally occurring radioactive materials (NORM) and extraction practices may possibly mobilise radionuclides into regional and local drinking water resources. Here, we establish baseline groundwater radon and uranium levels in shallow aquifers overlying a potential CSG target formation in the Richmond River Catchment, Australia. A total of 91 groundwater samples from six different geological units showed highly variable radon activities (0.14-20.33 Bq/L) and uranium levels (0.001-2.77 μg/L) which were well below the Australian Drinking Water Guideline values (radon; 100 Bq/L and uranium; 17 μg/L). Therefore, from a radon and uranium perspective, the regional groundwater does not pose health risks to consumers. Uranium could not explain the distribution of radon in groundwater. Relatively high radon activities (7.88 ± 0.83 Bq/L) in the fractured Lismore Basalt aquifer coincided with very low uranium concentrations (0.04 ± 0.02 μg/L). In the Quaternary Sediments aquifers, a positive correlation between U and HCO3(-) (r(2) = 0.49, p uranium was present as uranyl-carbonate complexes. Since NORM are often enriched in target geological formations containing unconventional gas, establishing radon and uranium concentrations in overlying aquifers comprises an important component of baseline groundwater investigations. Copyright © 2016 Elsevier Ltd. All rights reserved.

Microbial DNA; a possible tracer of groundwater

Science.gov (United States)

Sugiyama, Ayumi; Segawa, Takuya; Furuta, Tsuyumi; Nagaosa, Kazuyo; Tsujimura, Maki; Kato, Kenji

2017-04-01

chemical materials dissolved in groundwater. Though viral particle was employed as a tracer to chase the movement of groundwater, it doesn't tell the chemical and physical environmental condition where the particle was incorporated into groundwater. Thus, we propose microbial DNA as a new tracer to track the route of groundwater.

Controls on groundwater flow in the Bengal Basin of India and Bangladesh: regional modeling analysis

Science.gov (United States)

Michael, Holly A.; Voss, Clifford I.

2009-11-01

Groundwater for domestic and irrigation purposes is produced primarily from shallow parts of the Bengal Basin aquifer system (India and Bangladesh), which contains high concentrations of dissolved arsenic (exceeding worldwide drinking water standards), though deeper groundwater is generally low in arsenic. An essential first step for determining sustainable management of the deep groundwater resource is identification of hydrogeologic controls on flow and quantification of basin-scale groundwater flow patterns. Results from groundwater modeling, in which the Bengal Basin aquifer system is represented as a single aquifer with higher horizontal than vertical hydraulic conductivity, indicate that this anisotropy is the primary hydrogeologic control on the natural flowpath lengths. Despite extremely low hydraulic gradients due to minimal topographic relief, anisotropy implies large-scale (tens to hundreds of kilometers) flow at depth. Other hydrogeologic factors, including lateral and vertical changes in hydraulic conductivity, have minor effects on overall flow patterns. However, because natural hydraulic gradients are low, the impact of pumping on groundwater flow is overwhelming; modeling indicates that pumping has substantially changed the shallow groundwater budget and flowpaths from predevelopment conditions.

Controls on groundwater flow in the Bengal Basin of India and Bangladesh: Regional modeling analysis

Science.gov (United States)

Michael, H.A.; Voss, C.I.

2009-01-01

Groundwater for domestic and irrigation purposes is produced primarily from shallow parts of the Bengal Basin aquifer system (India and Bangladesh), which contains high concentrations of dissolved arsenic (exceeding worldwide drinking water standards), though deeper groundwater is generally low in arsenic. An essential first step for determining sustainable management of the deep groundwater resource is identification of hydrogeologic controls on flow and quantification of basin-scale groundwater flow patterns. Results from groundwater modeling, in which the Bengal Basin aquifer system is represented as a single aquifer with higher horizontal than vertical hydraulic conductivity, indicate that this anisotropy is the primary hydrogeologic control on the natural flowpath lengths. Despite extremely low hydraulic gradients due to minimal topographic relief, anisotropy implies large-scale (tens to hundreds of kilometers) flow at depth. Other hydrogeologic factors, including lateral and vertical changes in hydraulic conductivity, have minor effects on overall flow patterns. However, because natural hydraulic gradients are low, the impact of pumping on groundwater flow is overwhelming; modeling indicates that pumping has substantially changed the shallow groundwater budget and flowpaths from predevelopment conditions. ?? Springer-Verlag 2009.

Nutrients fluxes from groundwater discharge into Mangueira Lagoon (Rio Grande do Sul, Brazil); Fluxos de nutrientes associados as descargas de agua subterranea para a Lagoa Mangueira (Rio Grande do Sul, Brasil)

Energy Technology Data Exchange (ETDEWEB)

Andrade, Carlos F.F.; Niencheski, Luis F.H.; Attisano, Karina K.; Milani, Marcio R., E-mail: pgofcfa@furg.br [Instituto de Oceanografia, Universidade Federal do Rio Grande, Campus Carreiros, Rio Grande, RS (Brazil); Santos, Isaac R. [Department of Oceanography, Florida State University, Tallahassee, FL (United States); Milani, Idel C. [Departamento de Engenharia Hidrica, Centro de Desenvolvimento Tecnologico, Universidade Federal de Pelotas, Campus Porto, Pelotas, RS (Brazil)

2012-07-01

This study assesses the importance of groundwater discharge to dissolved nutrient levels in Mangueira Lagoon. A transect of an irrigation canal in the margin of Lagoon demonstrated a strong geochemical gradient due to high groundwater inputs in this area. Using {sup 222}Rn as a quantitative groundwater tracer, we observed that the flux of dissolved inorganic nitrogen (DIN), silicate and phosphate (1178 and 1977; 26190 and 35652; 167 and 188 mol d{sup -1} for winter and summer, respectively) can continually supply/sustain primary production. The irrigation canals act as an artificial underground tributary and represent a new source of nutrients to coastal lagoons. (author)

Quantifying shallow and deep groundwater inputs to rivers with groundwater dating in hydrological observatories.

Science.gov (United States)

Aquilina, Luc; Marçais, Jean; Gauvain, Alexandre; Kolbe, Tamara; de Dreuzy, Jean-Raynald; Labasque, Thierry; Abbott, Benjamin W.; Vergnaud, Virginie; Chatton, Eliot; Thomas, Zahra; Ruiz, Laurent; Bour, Olivier; Pinay, Gilles

2017-04-01

River water derives in part from groundwater—water that has spent some time in the subsurface (e.g. soil, unsaturated zone, saturated zone). However, because groundwater residence times vary from months to millennia, determining the proportion of shallow and deep groundwater contribution can be challenging. Groundwater dating with anthropogenic gases and natural geochemical tracers can decipher the origin of groundwater contribution to rivers, particularly when repeat samplings are carried out in different hydrological conditions. Here, we present two different applications of this approach from three hydrological observatories (H+ hydrogeological network; Aghrys and Armorique observatories) in western France, all these observatories belonging to the OZCAR national network. We carried out a regional investigation of mean groundwater ages in hard rock aquifers in Brittany, using long-term chronicles from hydrological observatories and regional monitoring sites. We determined the mean residence-time (RT) and annual renewal rate (RR) of four compartments of these aquifers: the direct contribution of a very young water component (i.e. RT less than 1-2 yr), the upper variably saturated zone (RR 27-33%), the weathered layer (RR 1.8-2.1%) and the fractured zone (RR 0.1%). From these values and a nitrate chronicle, we were able to determine the respective contributions of each compartment to the largest river in Brittany, the Vilaine, which drains 30% of the region. We found that the deep fractured compartment with very slow renewal times contributed to 25-45% of river water in winter and 30-60% in summer. The very young water which includes direct precipitation and soil fluxes constituted 40-65% of the winter river water (Aquilina et al., 2012). To complement these estimates, we investigated the relationship between dissolved silica and groundwater age in the Armorique hydrological observatory in northern Brittany. We computed the silica concentration expected along the

Hydrogeochemical characteristics of groundwater in selected areas of NWFP

International Nuclear Information System (INIS)

Akram, W.; Sajjad, M.I.; Sheikh, M.R.; Iqbal, M.Z.

1998-01-01

Chemical composition of ground water in selected area of NWFP (Pakistan) was investigated. Water samples were collected from existing open well, tube wells, springs and the river Indus. Important physico-chemical parameter like temperature, pH and electrical conductivity were measured in situ. All the collected samples were analysed for their dissolved chemical constituents (Na, K, Ca, Mg, Cl, HCO/sub 3/, NO/sub 3, SO/sub 4///0 in the laboratory. Different standard technique likes atomic absorption spectrophotometry, UV-visible spectrophotometry, ion selective electrodes and titrimetry were used for sample analyses. Data was used to study the recent trends of ground water chemistry in these areas. Chemical quality of groundwater was evaluated to determine its suitability for drinking purposes by comparing with WHO standards. It was found that groundwater in these areas meets the norms of good quality drinking water except in very few locations. Different compositional types of water were also identified. It was observed that Ca is the dominant cation at most of the locations which is balanced by HCO/sub 3/ giving rise to calcium bicarbonate type groundwater. At few locations groundwater of sodium sodium bicarbonate or mixed type was also encountered. (author)

Hydrothermal waste package interactions with methane-containing basalt groundwater

International Nuclear Information System (INIS)

McGrail, B.P.

1984-11-01

Hydrothermal waste package interaction tests with methane-containing synthetic basalt groundwater have shown that in the absence of gamma radiolysis, methane has little influence on the glass dissolution rate. Gamma radiolysis tests at fluxes of 5.5 x 10 5 and 4.4 x 10 4 R/hr showed that methane-saturated groundwater was more reducing than identical experiments where Ar was substituted for CH 4 . Dissolved methane, therefore, may be beneficial to the waste package in limiting the solubility of redox sensitive radionuclides such a 99 Tc. Hydrocarbon polymers known to form under the irradiation conditions of these tests were not produced. The presence of the waste package constituents apparently inhibited the formation of the polymers, however, the mechanism which prevented their formation was not determined

Geomicrobial investigations of groundwaters from Olkiluoto, Haestholmen, Kivetty and Romuvaara, Finland

Energy Technology Data Exchange (ETDEWEB)

Haveman, S.A.; Pedersen, K. [Goeteborg Univ. (Sweden); Ruotsalainen, P. [Fintact Oy, Helsinki (Finland)

1998-08-01

Groundwater from four deep hard rock sites being considered for nuclear waste disposal in Finland (Olkiluoto, Haestholmen, Kivetty and Romuvaara) were investigated for microbial populations. Bacteria will be present in a waste disposal vault, so it is important to understand the microbiology of any potential site. Groundwater samples were collected from 200 to 950 m depth and included fresh, brackish and saline waters. Samples were collected with a pressurized groundwater sampler, PAVE, which is an excellent tool for microbiological sampling. Total cell numbers were typical for deep groundwater, 105 to 106 cells/ml. Growth media designed using groundwater chemistry data were used for enumeration of methanogens, acetogens, sulfate reducing bacteria (SRB) and iron reducing bacteria (IRB). Microbial populations varied between sites. Iron sulfide fracture minerals are common in the brackish high sulfate groundwaters of Olkiluoto, where SRB predominated. Haestholmen groundwater has high dissolved iron, iron hydroxide fracture minerals and IRB were the main microbial population. Kivetty and Romuvaara had mixed populations. It has been proposed that deep subsurface ecosystems are based on hydrogen and carbon dioxide which provide energy and carbon to support the food chain. Signs of such an ecosystem were seen in Olkiluoto. More study is needed to understand the basis for deep subsurface life. From a microbiological point of view, all sites investigated are equally suitable for nuclear waste disposal. (orig.) 66 refs.

Geomicrobial investigations of groundwaters from Olkiluoto, Haestholmen, Kivetty and Romuvaara, Finland

International Nuclear Information System (INIS)

Haveman, S.A.; Pedersen, K.; Ruotsalainen, P.

1998-08-01

Groundwater from four deep hard rock sites being considered for nuclear waste disposal in Finland (Olkiluoto, Haestholmen, Kivetty and Romuvaara) were investigated for microbial populations. Bacteria will be present in a waste disposal vault, so it is important to understand the microbiology of any potential site. Groundwater samples were collected from 200 to 950 m depth and included fresh, brackish and saline waters. Samples were collected with a pressurized groundwater sampler, PAVE, which is an excellent tool for microbiological sampling. Total cell numbers were typical for deep groundwater, 105 to 106 cells/ml. Growth media designed using groundwater chemistry data were used for enumeration of methanogens, acetogens, sulfate reducing bacteria (SRB) and iron reducing bacteria (IRB). Microbial populations varied between sites. Iron sulfide fracture minerals are common in the brackish high sulfate groundwaters of Olkiluoto, where SRB predominated. Haestholmen groundwater has high dissolved iron, iron hydroxide fracture minerals and IRB were the main microbial population. Kivetty and Romuvaara had mixed populations. It has been proposed that deep subsurface ecosystems are based on hydrogen and carbon dioxide which provide energy and carbon to support the food chain. Signs of such an ecosystem were seen in Olkiluoto. More study is needed to understand the basis for deep subsurface life. From a microbiological point of view, all sites investigated are equally suitable for nuclear waste disposal. (orig.)

Filter-separable constituents of groundwater from the Columbia River plateau

International Nuclear Information System (INIS)

Seitz, M.G.; Boggs, S. Jr.

1984-01-01

The purpose of this procedure is to prepare groundwaters from the Columbia River basalt, northeastern Oregon, for batch partitioning experiments by concentration dissolved organic carbon (DOC) in water samples by ultrafiltration. Water samples were double-filtered through 0.4-μm Nuclepore polycarbonate filters to remove particulates before beginning the ultrafiltration process. The results of these experiments do not indicate a consistent relation between the distribution of americium with coexisting basalt and groundwater and the DOC content of the groundwater at 25 0 C, but there is some indication of increasing sorption of americium on basalt with increasing DOC at 90 0 C. However, any simple interpretation of the effects of DOC on the sorption behavior of americium must be made with caution, as there are other variables in the chemistry of the groundwaters that may also have important controls on this process. Another important observation from this set of experiments is that ultrafiltration does not seem to be an effective means of concentrating DOC without affecting the other trace constituents of groundwaters. The observed fractionation of groundwater chemistry as a result of the ultrafiltration procedure is not yet understood. However, for further progress in experiments of this type, it may be necessary to develop an alternative means of concentrating organic compounds that would allow the maintenance of constant values of other trace constituents as an experimental control

Groundwater salinity at Olkiluoto and its effects on a spent fuel repository

Energy Technology Data Exchange (ETDEWEB)

Vieno, T. [VTT Energy, Espoo (Finland)

2000-06-01

The Olkiluoto island rose from the Baltic Sea 2500 to 3000 years ago. The layered sequence of groundwaters can be related to climatic and shoreline changes from modern tune through former Baltic stages to the deglaciation phase about 10 000 years ago and even to preglacial times. Fresh groundwater is found to the depth of about 150 metres, brackish between 100 and 400 metres, deeper groundwaters are saline. At the depth of 500 meters, the content of Total Dissolved Solids (TDS) varies between 10 and 25 g/l. The most saline waters at depths greater than 800 metres have TDS values between 30 and 75 g/l. These deep saline waters seem to have been undisturbed during the most recent glaciation and even much longer in the past. Today fresh water infiltrating at the surface gradually displaces brackish and saline groundwater in the bedrock. Due to the still ongoing postglacial land uplift, Olkiluoto is likely to become an inland site with brackish or fresh groundwater at the depth of 500 metres within the next 10 000 years. During the construction and operation phases groundwater will be drawn into the repository from the surrounding bedrock. As a consequence, more saline groundwaters, presently laying 100 to 200 metres below the repository level, may rise to the disposal level. After the closing of the repository the salinity distribution will gradually return towards the natural state. During the glacial cycle groundwater salinity may increase, for example, during freezing of groundwater into permafrost, when dissolved solids concentrate in the remaining water phase, and in a situation where deep saline groundwaters from under the centre of the glacier are pushed to the upper parts of the bedrock at the periphery of the glacier. The most significant open issue related to saline groundwater is the performance of the tunnel backfill which in the BS-3 concept has been planned to consist of a mixture of crushed rock and 10-30% of bentonite. Saline groundwater may

A city scale study on the effects of intensive groundwater heat pump systems on heavy metal contents in groundwater.

Science.gov (United States)

García-Gil, Alejandro; Epting, Jannis; Garrido, Eduardo; Vázquez-Suñé, Enric; Lázaro, Jesús Mateo; Sánchez Navarro, José Ángel; Huggenberger, P; Calvo, Miguel Ángel Marazuela

2016-12-01

As a result of the increasing use of shallow geothermal resources, hydraulic, thermal and chemical impacts affecting groundwater quality can be observed with ever increasing frequency (Possemiers et al., 2014). To overcome the uncertainty associated with chemical impacts, a city scale study on the effects of intensive geothermal resource use by groundwater heat pump systems on groundwater quality, with special emphasis on heavy metal contents was performed. Statistical analysis of geochemical data obtained from several field campaigns has allowed studying the spatiotemporal relationship between temperature anomalies in the aquifer and trace element composition of groundwater. The relationship between temperature and the concentrations of trace elements resulted in weak correlations, indicating that temperature changes are not the driving factor in enhancing heavy metal contaminations. Regression models established for these correlations showed a very low reactivity or response of heavy metal contents to temperature changes. The change rates of heavy metal contents with respect to temperature changes obtained indicate a low risk of exceeding quality threshold values by means of the exploitation regimes used, neither producing nor enhancing contamination significantly. However, modification of pH, redox potential, electrical conductivity, dissolved oxygen and alkalinity correlated with the concentrations of heavy metals. In this case, the change rates of heavy metal contents are higher, with a greater risk of exceeding threshold values. Copyright © 2016 Elsevier B.V. All rights reserved.

Assessing biosynthetic potential of agricultural groundwater through metagenomic sequencing: A diverse anammox community dominates nitrate-rich groundwater.

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William B Ludington

Full Text Available Climate change produces extremes in both temperature and precipitation causing increased drought severity and increased reliance on groundwater resources. Agricultural practices, which rely on groundwater, are sensitive to but also sources of contaminants, including nitrate. How agricultural contamination drives groundwater geochemistry through microbial metabolism is poorly understood.On an active cow dairy in the Central Valley of California, we sampled groundwater from three wells at depths of 4.3 m (two wells and 100 m (one well below ground surface (bgs as well as an effluent surface water lagoon that fertilizes surrounding corn fields. We analyzed the samples for concentrations of solutes, heavy metals, and USDA pathogenic bacteria of the Escherichia coli and Enterococcus groups as part of a long term groundwater monitoring study. Whole metagenome shotgun sequencing and assembly revealed taxonomic composition and metabolic potential of the community.Elevated nitrate and dissolved organic carbon occurred at 4.3m but not at 100m bgs. Metagenomics confirmed chemical observations and revealed several Planctomycete genomes, including a new Brocadiaceae lineage and a likely Planctomycetes OM190, as well novel diversity and high abundance of nano-prokaryotes from the Candidate Phyla Radiation (CPR, the Diapherotrites, Parvarchaeota, Aenigmarchaeota, Nanoarchaeota, Nanohaloarchaea (DPANN and the Thaumarchaeota, Aigarchaeota, Crenarchaeota, Korarchaeota (TACK superphyla. Pathway analysis suggests community interactions based on complimentary primary metabolic pathways and abundant secondary metabolite operons encoding antimicrobials and quorum sensing systems.The metagenomes show strong resemblance to activated sludge communities from a nitrogen removal reactor at a wastewater treatment plant, suggesting that natural bioremediation occurs through microbial metabolism. Elevated nitrate and rich secondary metabolite biosynthetic capacity suggest

Evaluation of ground-water flow and solute transport in the Lompoc area, Santa Barbara County, California

Science.gov (United States)

Bright, Daniel J.; Nash, David B.; Martin, Peter

1997-01-01

Ground-water quality in the Lompoc area, especially in the Lompoc plain, is only marginally acceptable for most uses. Demand for ground water has increased for municipal use since the late 1950's and has continued to be high for irrigation on the Lompoc plain, the principal agricultural area in the Santa Ynez River basin. As use has increased, the quality of ground water has deteriorated in some areas of the Lompoc plain. The dissolved-solids concentration in the main zone of the upper aquifer beneath most of the central and western plains has increased from less than 1,000 milligrams per liter in the 1940's to greater than 2,000 milligrams per liter in the 1960's. Dissolved- solids concentration have remained relatively constant since the 1960's. A three-dimensional finite-difference model was used to simulate ground-water flow in the Lompoc area and a two-dimensional finite-element model was used to simulate solute transport to gain a better understanding of the ground-water system and to evaluate the effects of proposed management plans for the ground-water basin. The aquifer system was simulated in the flow model as four horizontal layers. In the area of the Lompoc plain, the layers represent the shallow, middle, and main zones of the upper aquifer, and the lower aquifer. For the Lompoc upland and Lompoc terrace, the four layers represent the lower aquifer. The solute transport model was used to simulate dissolved-solids transport in the main zone of the upper aquifer beneath the Lompoc plain. The flow and solute-transport models were calibrated to transient conditions for 1941-88. A steady-state simulation was made to provide initial conditions for the transient-state simulation by using long-term average (1941-88) recharge rates. Model- simulated hydraulic heads generally were within 5 feet of measured heads in the main zone for transient conditions. Model-simulated dissolved- solids concentrations for the main zone generally differed less than 200milligrams

Modeling the long-term fate of agricultural nitrate in groundwater in the San Joaquin Valley, California

Science.gov (United States)

Chapelle, Francis H.; Campbell, Bruce G.; Widdowson, Mark A.; Landon, Mathew K.

2013-01-01

Nitrate contamination of groundwater systems used for human water supplies is a major environmental problem in many parts of the world. Fertilizers containing a variety of reduced nitrogen compounds are commonly added to soils to increase agricultural yields. But the amount of nitrogen added during fertilization typically exceeds the amount of nitrogen taken up by crops. Oxidation of reduced nitrogen compounds present in residual fertilizers can produce substantial amounts of nitrate which can be transported to the underlying water table. Because nitrate concentrations exceeding 10 mg/L in drinking water can have a variety of deleterious effects for humans, agriculturally derived nitrate contamination of groundwater can be a serious public health issue. The Central Valley aquifer of California accounts for 13 percent of all the groundwater withdrawals in the United States. The Central Valley, which includes the San Joaquin Valley, is one of the most productive agricultural areas in the world and much of this groundwater is used for crop irrigation. However, rapid urbanization has led to increasing groundwater withdrawals for municipal public water supplies. That, in turn, has led to concern about how contaminants associated with agricultural practices will affect the chemical quality of groundwater in the San Joaquin Valley. Crop fertilization with various forms of nitrogen-containing compounds can greatly increase agricultural yields. However, leaching of nitrate from soils due to irrigation has led to substantial nitrate contamination of shallow groundwater. That shallow nitrate-contaminated groundwater has been moving deeper into the Central Valley aquifer since the 1960s. Denitrification can be an important process limiting the mobility of nitrate in groundwater systems. However, substantial denitrification requires adequate sources of electron donors in order to drive the process. In many cases, dissolved organic carbon (DOC) and particulate organic carbon

Groundwater Quality Improvement by Using Aeration and Filtration Methods

OpenAIRE

Nik N. Nik Daud; Nur H. Izehar; B. Yusuf; Thamer A. Mohamed; A. Ahsan

2013-01-01

An experiment was conducted using two aeration methods (water-into-air and air-into-water) and followed by filtration processes using manganese greensand material. The properties of groundwater such as pH, dissolved oxygen, turbidity and heavy metal concentration (iron and manganese) will be assessed. The objectives of this study are i) to determine the effective aeration method and ii) to assess the effectiveness of manganese greensand as filter media in removing iron an...

Genesis and transport of hexavalent chromium in the system ophiolitic rocks - groundwater

Science.gov (United States)

Shchegolikhina, Anastasia; Guadagnini, Laura; Guadagnini, Alberto

2015-04-01

Our study aims at contributing to the quantification and characterization of chromium transport processes from host rocks and soil matrices to groundwater. We focus on dissolved hexavalent chromium detected in groundwaters of geological regions with ophiolitic rocks (ophiolites and serpentinites) inclusions due to its critical ecological impact. (Oze et al., 2004). Despite the large number of analyses on the occurrence of high concentrations of hazardous hexavalent chromium ions in natural waters, only few studies were performed with the objective of identifying and investigating the geochemical reactions which could occur in the natural system rock - groundwater - dissolved chromium (Fantoni et al., 2002, Stephen and James, 2004, Lelli et al., 2013). In this context, there is a need for integration of results obtained from diverse studies in various regions and settings to improve our knowledge repository. Our theoretical analyses are grounded and driven by practical scenarios detected in subsurface reservoirs exploited for civil and industrial use located in the Emilia-Romagna region (Italy). Available experimental datasets are complemented with data from other international regional-scale settings (Altay mountains region, Russia). Modeling of chromium transformation and migration particularly includes characterization of the multispecies geochemical system. A key aspect of our study is the analysis of the complex competitive sorption processes governing heavy metal evolution in groundwater. The results of the research allow assessing the critical qualitative features of the mechanisms of hexavalent chromium ion mobilization from host rocks and soils and the ensuing transformation and migration to groundwater under the influence of diverse environmental factors. The study is then complemented by the quantification of the main sources of uncertainty associated with prediction of heavy metal contamination levels in the groundwater system explored. Fantoni, D

Arsenic transport in groundwater, surface water, and the hyporheic zone of a mine-influenced stream-aquifer system

OpenAIRE

Brown, Brendan

2005-01-01

We investigated the transport of dissolved arsenic in groundwater, surface water and the hyporheic zone in a stream-aquifer system influenced by an abandoned arsenopyrite mine. Mine tailing piles consisting of a host of arsenic-bearing minerals including arsenopyrite and scorodite remain adjacent to the stream and represent a continuous source of arsenic. Arsenic loads from the stream, springs, and groundwater were quantified at the study reach on nine dates from January to August 2005 and ...

Application of krypton-85 in groundwater dating

International Nuclear Information System (INIS)

Rozanski, K.

1979-01-01

The method for determination 85 Kr activity in groundwater and its application in isotope hydrology is presented. Various aspects of 85 Kr presence in the earth's ecosphere are discussed in the first part of the paper. The method for 85 Kr activity measurement in groundwater is presented in the second part of the paper. Analytical procedure consists of the following steps: extraction of the gases dissolved in water sample, separation of the Ar+Kr mixture from the gases, 85 Kr activity measurement in miniature proportional counter, mass spectrometry determination of the krypton gas volume in the proportional counter. About 7 days is necessary for complete analysis of one sample - the error of analysis not exceeds 10 per cent. The results of 85 Kr activity measurements (together with tritium and carbon 14 C determinations) in 14 different water samples allowed to verify usefulness of 85 Kr dating of young water. (author)

Arsenic in groundwaters of rural India: its geochemistry and mitigation approaches

Science.gov (United States)

Chatterjee, Debashis; Majumder, Santanu; Kundu, Amit; Barman, Sandipan; Chatterjee, Debankur; Bhattacharya, Prosun

2016-04-01

During the last few decades, arsenic (As) has been recognized as the most threatening contaminant in natural waters (especially groundwater). It has become a menace to the health of millions of people worldwide. Many large and small communities experience As contamination in groundwater and/or drinking water supplies in south-east Asia and the problem is grave in West Bengal and Bangladesh (Bengal Delta Plain, BDP) both in terms of human exposure as well as spatial coverage. It is frequently observed that As concentration in contaminated wells exceeds both WHO guideline value (10 mg/l) and stipulated National standard (50 mg/l) for both Bangladesh and India. Dissolved forms of As in the BDP water include arsenite (~50-70%), arsenate (~30-50%) and ultra-trace amount of monomethylarsonic acid and dimethylarsinic acid. Arsenite and arsenate species can interchange depending on redox potential (Eh), pH and biological processes. The prevailing local geomorphological features (surface water, sanitation, agricultural activity) can also influence the mobilization of As in addition to the dominant geological factors. Therefore, the local sedimentology and hydrogeology should also be given importance prior to implement or consider any policy to mitigate the As contamination of groundwater. Conventional treatment techniques to remove As from groundwater are costly and difficult to practice in rural areas of the BDP. There are several techniques available for groundwater As removal. Iron and Alum coagulation, softening [mediated by calcite or Mg(OH)2 formation], by reverse osmosis, using zero-valent iron and nanoparticulate zero-valent iron, several natural/synthetic metal oxides, naturally found minerals like siderite, hematite, using iron doped activated carbons, development of bio-physicochemical techniques, using granular TiO2 adsorbent are some of the many proposed removal techniques investigated by various researchers. Instead of using hazardous chemicals (e.g. chlorine

Using Spatial Clustering in Forecasting Groundwater Quality Parameters by ANFIS

Directory of Open Access Journals (Sweden)

MohammadTaghi Alami

2016-07-01

Full Text Available Groundwater is a major source of water supply for domestic, agricultural, and industrial uses; hence, its quality modeling is an important task in hydro-environmental studies. While many data-based models have been developed for this purpose, the performance of such data-based models can be drastically enhanced if they are based on temporal and spatial pre-processing. In this study, geostatistics tools (e.g., Co-Kriging, as spatial estimators, and self-organizing map (SOM, as a clustering technique, were employed in conjunction with Adaptive Neuro-Fuzzy Inference System (ANFIS for the temporal forecasting of such quality parameters as electrical conductivity (EC and total dissolved solids (TDS of the groundwater in Ardabil Plain. Using the results thus obtained, the impact of spatial data clustering was also investigated on the same parameters. The results showed that, if propoer input data are selected, the proposed spatial clustering technique is capable of imporving groundwater quality forecasts made by ANFIS.

Quantity and quality of groundwater discharge in a hypersaline lake environment

Science.gov (United States)

Anderson, R.B.; Naftz, D.L.; Day-Lewis, F. D.; Henderson, R.D.; Rosenberry, D.O.; Stolp, B.J.; Jewell, P.

2014-01-01

Geophysical and geochemical surveys were conducted to understand groundwater discharge to Great Salt Lake (GSL) and assess the potential significance of groundwater discharge as a source of selenium (Se). Continuous resistivity profiling (CRP) focusing below the sediment/water interface and fiber-optic distributed temperature sensing (FO-DTS) surveys were conducted along the south shore of GSL. FO-DTS surveys identified persistent cold-water temperature anomalies at 10 separate locations. Seepage measurements were conducted at 17 sites (mean seepage rate = 0.8 cm/day). High resistivity anomalies identified by the CRP survey were likely a mirabilite (Na2SO4·10H2O) salt layer acting as a semi-confining layer for the shallow groundwater below the south shore of the lake. Positive seepage rates measured along the near-shore areas of GSL indicate that a ∼1-m thick oolitic sand overlying the mirabilite layer is likely acting as a shallow, unconfined aquifer. Using the average seepage rate of 0.8 cm/day over an area of 1.6 km2, an annual Se mass loading to GSL of 23.5 kg was estimated. Determination of R/Ra values (calculated 3He/4He ratio over the present-day atmospheric 3He/4He ratio) 34S and δ18O isotopic values in samples of dissolved sulfate from the shallow groundwater below the mirabilite are almost identical to the isotopic signature of the mirabilite core material. The saturation index calculated for groundwater samples using PHREEQC indicates the water is at equilibrium with mirabilite. Water samples collected from GSL immediately off shore contained Se concentrations that were 3–4 times higher than other sampling sites >25 km offshore from the study site and may be originating from less saline groundwater seeps mixing with the more saline water from GSL. Additional evidence for mixing with near shore seeps is found in the δD and δ18O isotopic values and Br:Cl ratios. Geochemical modeling for a water sample collected in the vicinity of the study area

The discharge of nitrate-contaminated groundwater from developed shoreline to marsh-fringed estuary

Science.gov (United States)

Portnoy, J.W.; Nowicki, B.L.; Roman, C.T.; Urish, D.W.

1998-01-01

As residential development, on-site wastewater disposal, and groundwater contamination increase in the coastal zone, assessment of nutrient removal by soil and sedimentary processes becomes increasingly important. Nitrogen removal efficiency depends largely on the specific flow paths taken by groundwater as it discharges into nitrogen-limited estuarine waters. Shoreline salinity surveys, hydraulic studies, and thermal infrared imagery indicated that groundwater discharge into the Nauset Marsh estuary (Eastham, Massachusetts) occurred in high-velocity seeps immediately seaward of the upland-fringing salt marsh. Discharge was highly variable spatially and occurred through permeable, sandy sediments during low tide. Seepage chamber monitoring showed that dissolved inorganic nitrogen (principally nitrate) traversed nearly conservatively from the aquifer through shallow estuarine sediments to coastal waters at flux rates of 1–3 mmol m−2 h−1. A significant relationship between pore water NO3-N concentrations and NO3-N flux rates may provide a rapid method of estimating nitrogen loading from groundwater to the water column.

Estimation of the groundwater quality in the western part of Lipjan (Kosovo

Directory of Open Access Journals (Sweden)

Fatbardh Gashi

2015-12-01

Full Text Available The study of the effect of anthropogenic activity on the water quality was carried out in the western part of Lipjan (Kosovo. The software “Statistica 6.0” was used for calculations of basic statistical parameters and anomalies (extremes and outliers. The levels of some physicochemical parameters of groundwater are compared with the World Health Organization standards for drinking water. Our results show significant pollution (high values of electrical conductivity, total dissolved solids and consumption of KMnO4 of groundwaters as a result of anthropogenic activity coming from settlements, pollution of small rivers (Vodavoda and Grika and wastewaters in the surrounding area.

Integration of ground-water and vadose-zone geochemistry to investigate hydrochemical evolution

International Nuclear Information System (INIS)

Fisher, R.S.; Mullican, W.F.

1990-01-01

This paper summarizes the results of an extensive groundwater-sampling program conducted in the Hueco Bolson and Diablo Plateau area of West Texas. The origin, hydrochemical evolution, and age of groundwater in arid lands of Trans-Pecos Texas were investigated by combining mineralogic analyses of soils and aquifer matrix, chemical analyses of readily soluble materials in soils and water extracted from the thick, unsaturated zone, and chemical and isotopic analyses of groundwater from three principal aquifers, the Diablo Plateau, Hueco Bolson, and Rio Grande alluvial aquifers. Repeated groundwater sampling over a 3-year period and quarterly sampling of selected wells revealed no significant short-term chemical or isotopic variability. Groundwater ages range from recent to nearly 28,000 years; the distribution of ages reflects relative permeability (transmissivity) of the aquifers. Most groundwaters evolve from calcium-bicarbonate to sodium-sulfate types because of carbonate and sulfate mineral dissolution coupled with exchange of aqueous calcium and magnesium for sodium on clay minerals. Water in the Rio Grande alluvial aquifer evolved to a sodium-chloride type as a result of extensive evapotranspiration on irrigated fields. The appendices list detailed results of field measurements of temperature, pH, Eh, dissolved oxygen, and major ion concentrations

Photocatalytic degradation of dissolved organic matter in the ground water employing TiO2 film supported on stainless steel plate

International Nuclear Information System (INIS)

Andayani, W.; Sumartono, A.; Lindu, M.

2012-01-01

The Taman Palem Residences, Cengkareng, Indonesia has a groundwater problem as a main sources of drinking water in the area due to yellowish brown colour of the water, that may come from dissolved organic matter (DOM), humic substances. Photocatalytic degradation using TiO 2 coated on a stainless steel plate (8 x 8 cm) to degrade the dissolved organic matter was studied. Groundwater samples were collected at 150 m deep from Taman Palem Residences. The TiO 2 catalyst was made from deep coating in a sol-gel system of titanium (IV) diisopropoxidebisacetylacetonate (TAA) precursor and immobilized at stainless steel plate (8 x 8 cm), followed by calcination at 525°C. Two catalyst sheets were put in batch reactor containing groundwater. The ground water containing DOM were irradiated by UV black light at varying initial pH values i.e 5, 7 and 9. Sampling of solution was taken at the interval time of 0, 1, 2, 4, and 6 hours. DOM residu in water before and after irradiation were measured by spectrophotometer UV-Vis at 300 nm. Photocatalytic degradation of DOM was greater in acid solution than in basic solution. The determination of intermediate degradation products by HPLC revealed that oxalic acid was detected consistently. (author)

A Natural Analogue Approach for Discriminating Leaks of CO2 Stored Underground Using Groundwater Geochemistry Statistical Methods, South Korea

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Kwang-Koo Kim

2017-12-01

Full Text Available Carbon capture and storage (CCS is one of several useful strategies for capturing greenhouse gases to counter global climate change. In CCS, greenhouse gases such as CO2 that are emitted from stacks are isolated in underground geological storage. Natural analogue studies that can provide insights into possible geological CO2 storage sites, can deliver crucial information about the safety and security of geological sequestration, the long-term impact of CO2 storage on the environment, and the field operation and monitoring requirements for geological sequestration. This study adopted a probability density function (PDF approach for CO2 leakage monitoring by characterizing naturally occurring CO2-rich groundwater as an analogue that can occur around a CO2 storage site due to CO2 dissolving into fresh groundwater. Two quantitative indices, (QItail and QIshift, were estimated from the PDF test and were used to compare CO2-rich and ordinary groundwaters. Key geochemical parameters (pH, electrical conductance, total dissolved solids, HCO3−, Ca2+, Mg2+, and SiO2 in different geological regions of South Korea were determined through a comparison of quantitative indices and the respective distribution patterns of the CO2-rich and ordinary groundwaters.

Distributional patterns of arsenic concentrations in contaminant plumes offer clues to the source of arsenic in groundwater at landfills

Science.gov (United States)

Harte, Philip T.

2015-01-01

The distributional pattern of dissolved arsenic concentrations from landfill plumes can provide clues to the source of arsenic contamination. Under simple idealized conditions, arsenic concentrations along flow paths in aquifers proximal to a landfill will decrease under anthropogenic sources but potentially increase under in situ sources. This paper presents several conceptual distributional patterns of arsenic in groundwater based on the arsenic source under idealized conditions. An example of advanced subsurface mapping of dissolved arsenic with geophysical surveys, chemical monitoring, and redox fingerprinting is presented for a landfill site in New Hampshire with a complex flow pattern. Tools to assist in the mapping of arsenic in groundwater ultimately provide information on the source of contamination. Once an understanding of the arsenic contamination is achieved, appropriate remedial strategies can then be formulated.

Nitrate pollution of groundwater; all right…, but nothing else?

International Nuclear Information System (INIS)

Menció, Anna; Mas-Pla, Josep; Otero, Neus; Regàs, Oriol; Boy-Roura, Mercè

2016-01-01

Contamination from agricultural sources and, in particular, nitrate pollution, is one of the main concerns in groundwater management. However, this type of pollution entails the entrance of other substances into the aquifer, as well as it may promote other processes. In this study, we deal with hydrochemical and isotopic analysis of groundwater samples from four distinct zones in Catalonia (NE Spain), which include 5 different aquifer types, to investigate the influence of fertilization on the overall hydrochemical composition of groundwater. Results indicate that intense fertilizer application, causing high nitrate pollution in aquifers, also homogenize the contents of the major dissolved ions (i.e.; Cl - , SO 4 2- , Ca 2+ , Na + , K + , and Mg 2+ ). Thus, when groundwater in igneous and sedimentary aquifers is compared, significant differences are observed under natural conditions for Cl - , Na + and Ca 2+ (with p-values ranging from < 0.001 to 0.038), and when high nitrate concentrations occur, these differences are reduced (most p-values ranged between 0.054 and 0.978). Moreover, positive linear relationships between nitrate and some ions are found indicating the magnitude of the fertilization impact on groundwater hydrochemistry (with R 2 values of 0.490, 0.609 and 0.470, for SO 4 2- , Ca 2+ and Cl - , respectively). Nevertheless, the increasing concentration of specific ions is not only attributed to agricultural pollution, but to their enhancing effect upon the biogeochemical processes that control water-rock interactions. Such results raise awareness that these processes should be evaluated in advance in order to assess an adequate groundwater resources management. - Highlights: • The effects of nitrate pollution have been evaluated in five different aquifer types • Statistical and multivariate analyses are used to identify groundwater changes • Agricultural pollution modifies groundwater conditions and geochemical processes • Manure application

Hydrochemistry in the development of groundwater flow models at the Hanford site

International Nuclear Information System (INIS)

Early, T.O.

1986-01-01

Site characterization activities in progress at the Hanford Site include efforts to understand the groundwater flow regime within the Columbia River Basalt Group. Hydrochemical data from deep boreholes at Hanford suggest that groundwater has migrated upward at an unknown rate from the underlying sediments and mixed with more dilute shallow groundwaters within basalt aquifers. The driving force for upward flow is hypothesized to result from a regional flow system. Detailed analysis of deep groundwaters indicates that two major types exist. For example, water underlying the western part of the Site are sulfate poor and associated with relatively abundant dissolved methane. Deep groundwaters of the second type, lying to the east, are relatively sulfate rich but contain essentially no methane. Specific features of the source regions that yield these different geochemical types are poorly known but association of the western waters with methane-producing coal strata is proposed. At the level of the proposed repository evidence seems to point to little lateral flow. At shallower depths a somewhat more active lateral flow system is possible. The direction of lateral flow, whatever its rate, appears to be structurally controlled

Comparison of dissolved and particulate arsenic distributions in shallow aquifers of Chakdaha, India, and Araihazar, Bangladesh

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Ahmed Kazi M

2008-01-01

Full Text Available Abstract Background The origin of the spatial variability of dissolved As concentrations in shallow aquifers of the Bengal Basin remains poorly understood. To address this, we compare here transects of simultaneously-collected groundwater and aquifer solids perpendicular to the banks of the Hooghly River in Chakdaha, India, and the Old Brahmaputra River in Araihazar, Bangladesh. Results Variations in surface geomorphology mapped by electromagnetic conductivity indicate that permeable sandy soils are associated with underlying aquifers that are moderately reducing to a depth of 10–30 m, as indicated by acid-leachable Fe(II/Fe ratios 5 mg L-1. More reducing aquifers are typically capped with finer-grained soils. The patterns suggest that vertical recharge through permeable soils is associated with a flux of oxidants on the banks of the Hooghly River and, further inland, in both Chakdaha and Araihazar. Moderately reducing conditions maintained by local recharge are generally associated with low As concentrations in Araihazar, but not systematically so in Chakdaha. Unlike Araihazar, there is also little correspondence in Chakdaha between dissolved As concentrations in groundwater and the P-extractable As content of aquifer particles, averaging 191 ± 122 ug As/L, 1.1 ± 1.5 mg As kg-1 (n = 43 and 108 ± 31 ug As/L, 3.1 ± 6.5 mg As kg-1 (n = 60, respectively. We tentatively attribute these differences to a combination of younger floodplain sediments, and therefore possibly more than one mechanism of As release, as well as less reducing conditions in Chakdaha compared to Araihazar. Conclusion Systematic dating of groundwater and sediment, combined with detailed mapping of the composition of aquifer solids and groundwater, will be needed to identify the various mechanisms underlying the complex distribution of As in aquifers of the Bengal Basin.

Tracing coastal and estuarine groundwater discharge sources in a complex faulted and fractured karst aquifer system

Science.gov (United States)

Lagomasino, D.; Price, R. M.

2013-05-01

the western boundary of the reserve. Fresh groundwater and surface water from the southern evaporate region was characterized as a calcium sulfate water that was identified to contribute the southern portions of the Bahia de la Ascension. In the northern portions of the Bahia, surface and shallow groundwater chemistry was characterized as a more calcium bicarbonate-type water from the north that was undersaturated with respect to calcite. The implications from this preliminary study address the complex nature of the karst aquifer and help define groundwater flow pathways from the interior of the Yucatan peninsula to the coastal wetlands. Further investigation in the area will increase our understanding of the origin, transport, and fate of shallow groundwater; and identify areas of coastal brackish groundwater discharge from the mixing of fresh groundwater and seawater.

Groundwater quality from a part of Prakasam District, Andhra Pradesh, India

Science.gov (United States)

Subba Rao, N.

2018-03-01

Quality of groundwater is assessed from a part of Prakasam district, Andhra Pradesh, India. Groundwater samples collected from thirty locations from the study area were analysed for pH, electrical conductivity (EC), total dissolved solids (TDS), calcium (Ca2+), magnesium (Mg2+), sodium (Na+), potassium (K+), bicarbonate ( {HCO}3^{ - } ), chloride (Cl-), sulphate ( {SO}4^{2 - } ), nitrate ( {NO}3^{ - } ) and fluoride (F-). The results of the chemical analysis indicate that the groundwater is alkaline in nature and are mainly characterized by Na+- {HCO}3^{ - } and Na+-Cl- facies. Groundwater chemistry reflects the dominance of rock weathering and is subsequently modified by human activities, which are supported by genetic geochemical evolution and hydrogeochemical relations. Further, the chemical parameters (pH, TDS, Ca2+, Mg2+, Na+, {HCO}3^{ - } , Cl-, {SO}4^{2 - } , {NO}3^{ - } and F-) were compared with the drinking water quality standards. The sodium adsorption ratio, percent sodium, permeability index, residual sodium carbonate, magnesium ratio and Kelly's ratio were computed and USSL, Wilcox and Doneen's diagrams were also used for evaluation of groundwater quality for irrigation. For industrial purpose, the pH, TDS, {HCO}3^{ - } , Cl- and {SO}4^{2 - } were used to assess the impact of incrustation and corrosion activities on metal surfaces. As a whole, it is observed that the groundwater quality is not suitable for drinking, irrigation and industrial purposes due to one or more chemical parameters exceeding their standard limits. Therefore, groundwater management measures were suggested to improve the water quality.

Release of arsenic to deep groundwater in the Mekong Delta, Vietnam, linked to pumping-induced land subsidence.

Science.gov (United States)

Erban, Laura E; Gorelick, Steven M; Zebker, Howard A; Fendorf, Scott

2013-08-20

Deep aquifers in South and Southeast Asia are increasingly exploited as presumed sources of pathogen- and arsenic-free water, although little is known of the processes that may compromise their long-term viability. We analyze a large area (>1,000 km(2)) of the Mekong Delta, Vietnam, in which arsenic is found pervasively in deep, Pliocene-Miocene-age aquifers, where nearly 900 wells at depths of 200-500 m are contaminated. There, intensive groundwater extraction is causing land subsidence of up to 3 cm/y as measured using satellite-based radar images from 2007 to 2010 and consistent with transient 3D aquifer simulations showing similar subsidence rates and total subsidence of up to 27 cm since 1988. We propose a previously unrecognized mechanism in which deep groundwater extraction is causing interbedded clays to compact and expel water containing dissolved arsenic or arsenic-mobilizing solutes (e.g., dissolved organic carbon and competing ions) to deep aquifers over decades. The implication for the broader Mekong Delta region, and potentially others like it across Asia, is that deep, untreated groundwater will not necessarily remain a safe source of drinking water.

The immigration model and its implications of natural radionuclides of coastal groundwater in Xiamen

International Nuclear Information System (INIS)

Cai Minggang; Huang Yipu; Chen Min; Liu Guangshan

2004-01-01

The natural radionuclides in groundwater systems are considered to reside in three pools: dissolved, sorbed (on rock surface), and solid. Transfer of radionuclides between the dissolved and solid pools is accomplished chiefly by dissolution, (co-)precipitation and/or a-recoil. The mass balance equations model of the natural radionuclides of dissolved and adsorbed phase reservoir in groundwater is established by setting certain conditions and parameters. The modeling equations form the basic of our assessment of the effects of sorption-desorption, dissolution-precipitation, and advection-diffusion in radionuclide transport in the groundwater. The interaction between groundwater and rock in Xiamen coastal aquifers were studied quantitatively using this model, which gave us reasonable explanation for the spatial distribution of natural radium, radon isotopes activities and their activities ratio. α-recoil supply rates of 222 Rn (P r,Rn-222 ) and 224 Ra (P α,Ra-224 ) range from 0.09 x 10 3 to 3.44 x 10 3 atoms·m -3 ·s -1 and from 0.13 x l0 3 to 4.91 x 10 3 atoms·m -3 ·s -1 , respectively. P α,Ra-224 is also found to be larger than P r,Rn-222 in every station, revealing that aquifer solids contain more thorium than uranium in studied area. Both of P r,Rn-222 and P α,Ra-224 of coastal groundwater decreased seaward, revealing a-recoil supplying rates of 222 Rn and 224 Ra by aquifers rock decreased gradually, which gave good explanation of the spatial distribution characters of above two nuclides. P r,Rn-222 /A Rn-222 increase seaward from 0.3 to 0.9 along the major paths, with the average value of 0.6. Such results reveal that the primary source of groundwater 222 Rn in these areas is α-recoil of 226 Ra decay in solid pool, and its relative increase along the paths. Another source of 222 Rn is 226 Ra decay in tile sorbed pool (R f,Ra-226 ·A Ra-226 ), which attributes about 40 percent of total source of coastal groundwater 222 Rn. P α,Ra-224 /A Ra-224 ranges

The immigration model and its implications of natural radionuclides of coastal groundwater in Xiamen

International Nuclear Information System (INIS)

Cai Minggang; Huang Yipu; Chen Min; Liu Guangshan

2005-01-01

The natural radionuclides in groundwater systems are considered to reside in three pools: dissolved, sorbed (on rock surface), and solid. Transfer of radionuclides between the dissolved and solid pools is accomplished chiefly by dissolution. (co-)precipitation and/or α-recoil. The mass balance equations model of the natural radionuclides of dissolved and adsorbed phase reservoir in groundwater is established by setting certain conditions and parameters. The modeling equations form the basic of our assessment of the effects of sorption-desorption, dissolution-precipitation, and advection-diffusion in radionuclide transport in the groundwater. The interaction between groundwater and rock in Xiamen coastal aquifers were studied quantitatively using this model, which gave us reasonable explanation for the spatial distribution of natural radium, radon isotopes activities and their activities ratio. α-recoil supply rates of 222 Rn (P r,Rn-22 -2) and 224 Ra (P a,Ra-224 ) range from 0.09 x l0 3 to 3.44 x 10 3 atoms·m -3 ·s -1 and from 0.13 x 10 3 to 4.91 x 10 3 x 10 3 atoms·m -3 ·s -1 , respectively. P a,Ra-224 is also found to be larger than P r,Rn-222 in every station, revealing that aquifer solids contain more thorium than uranium in studied area. Both of P r,Rn-222 and P a,Ra-224 of coastal groundwater decreased seaward, revealing α-recoil supplying rates of 222 Rn and 224 Ra by aquifers rock decreased gradually, which gave good explanation of the spatial distribution characters of above two nuclides. P r,Rn-222 /A Rn-222 increase seaward from 0.3 to 0.9 along the major paths, with the average value of 0.6, Such results reveal that the primary source of groundwater 222 Rn in these areas is α-recoil of 226 Ra decay in solid pool, and its relative increase along the paths. Another source of 222 Rn is 226 Ra decay in the sorbed pool (R f,Ra-226 ·A Ra-226 ), which attributes about 40 per cent of total source of coastal groundwater 222 Rn. P α,Ra-224 /A Ra-224

Groundwater denitrification in two agricultural river catchments: influence of hydro-geological setting and aquifer geochemistry

Science.gov (United States)

McAleer, Eoin; Mellander, Per-Erik; Coxon, Catherine; Richards, Karl G.; Jahangir, Mohammad M. R.

2015-04-01

Identifying subsurface environments with a natural capacity for denitrification is important for improving agricultural management. At the catchment scale, a complex hierarchy of landscape, hydro-geological and physico-chemical characteristics combine to affect the distribution of groundwater nitrate (NO3-). This study was conducted along four instrumented hillslopes in two ca. 10km2 agricultural river catchments in Ireland, one dominated by arable and one by grassland agriculture. Both catchments are characterised by well drained soils, but have differing aquifer characteristics. The arable catchment is underlain by weathered Ordovician slate bedrock which is extensively fractured with depth. The grassland catchment is characterised by Devonian sandstone bedrock, exhibiting both lateral (from upslope to near stream) and vertical variations in permeability along each hillslope. The capacity for groundwater denitrification was assessed by examining the concentration and distribution patterns of N species (total nitrogen, nitrate, nitrite, ammonium), dissolved organic carbon (DOC), dissolved oxygen (DO) and redox potential (Eh) in monthly samples from shallow and deep groundwater piezometers (n=37). Additionally, the gaseous products of denitrification: nitrous oxide (N2O) and excess dinitrogen (excess N2) were measured seasonally using gas chromatography and membrane inlet mass spectroscopy, respectively. The slate catchment was characterised by uniformity, both laterally and vertically, in aquifer geochemistry and gaseous denitrification products. The four year spatial mean groundwater NO3--N concentration was 6.89 mg/l and exhibited low spatial and temporal variability (temporal SD: 1.19 mg/l, spatial SD: 1.185 mg/l). Elevated DO concentrations (mean: 9.75 mg/l) and positive Eh (mean: +176.5mV) at all sample horizons indicated a setting with little denitrification potential. This non-reducing environment was reflected in a low accumulation of denitrification

NMR Based Sensors for In Situ Monitoring of Changes in Groundwater Chemistry

Science.gov (United States)

2017-04-21

check on the sensor accuracy. Alternatively, sampling of plumes with temporally variable behavior (e.g., seasonal changes in groundwater flow ...Oxygen Samples were prepared with high concentrations of dissolved oxygen by bubbling compressed gas through samples of deionized water. Samples with...sensitive polymers due to the presence of multiple relaxation domains (i.e. the observed relaxation behaviour is the product of multiple processes

Chlorine isotopes and their application to groundwater dating at Olkiluoto

International Nuclear Information System (INIS)

Gascoyne, M.

2014-09-01

The chlorine isotopes 36 Cl and 37 Cl have been shown to be useful tracers of groundwater, and for investigations of sources of dissolved Cl, mixing of fluids, water-rock interactions in sedimentary environments and in identifying solute sources and transport mechanisms. In addition, the radioactive isotope, 36 Cl, is a useful tracer for determining the residence time of groundwater. This report examines the results of Cl isotopic analysis of groundwaters from as deep as 1000 m at the Olkiluoto site in southwest Finland. Thirty-four samples were analysed for 36 Cl/Cl and 29 were analysed for 37 Cl (expressed as δ 37 Cl). The value δ 37 Cl was found to stabilize at higher salinities and the maximum range of δ 37 Cl was from about - 0.6 to +0.6 per mille. Because of this limited range and the relatively large error margins associated with the δ 37 Cl measurement, the usefulness of this ratio appears to be limited. Therefore, the main part of this report is largely focused on 36 Cl. Estimation of residence time of 36 Cl gives results that support the presence of at least five groundwater types at Olkiluoto. The consistency of 36 Cl/Cl ratios in groundwaters of several widely separated, deep locations and different rock compositions, suggests that these deeper groundwaters are in secular equilibrium and, therefore, likely to be older than 1.5 million years. (orig.)

Groundwater quality around Tummalapalle area, Cuddapah District, Andhra Pradesh, India

Science.gov (United States)

Sreedhar, Y.; Nagaraju, A.

2017-11-01

The suitability of groundwater for drinking and irrigation was assessed in Tummalapalle area. Forty groundwater samples were analysed for major cations, anions and other parameters such as pH, electrical conductivity, total dissolved solids (TDS), total alkalinity and total hardness (TH). The parameters such as sodium adsorption ratio, adjusted sodium adsorption ratio (adj.SAR), per cent sodium, potential salinity, residual sodium carbonate, non-carbonate hardness, Kelly's ratio and permeability index were calculated for the evaluation of irrigation water quality. Groundwater chemistry was also analysed by statistical analysis, USSL, Wilcox, Doneen, Piper and Chadhas diagrams, to find out their suitability for irrigation. TDS and TH were used as main parameters to interpret the suitability of groundwater for drinking purpose. The correlation coefficient matrix between the hydrochemical parameters was carried out using Pearson's correlation to infer the possible water-rock interactions responsible for the variation of groundwater chemistry and this has been supported by Gibbs diagram. The results indicate that the groundwater in Tummalapalle area is alkaline in nature. Ca-Mg-HCO3 is the dominant hydrogeochemical facies. Water chemistry of the study area strongly reflects the dominance of weathering of rock-forming minerals such as bicarbonates and silicates. All parameters and diagrams suggest that the water samples of the study are good for irrigation, and the plots of TDS and TH suggest that 12.5% of the samples are good for human consumption.

Imaging subsurface migration of dissolved CO2 in a shallow aquifer using 3-D time-lapse electrical resistivity tomography

DEFF Research Database (Denmark)

Auken, Esben; Doetsch, Joseph; Fiandaca, Gianluca

2014-01-01

Contamination of groundwater by leaking CO2 is a potential risk of carbon sequestration. With the help of a field experiment in western Denmark, we investigate to what extent surface electrical resistivity tomography (ERT) can detect and image dissolved CO2 in a shallow aquifer. For this purpose...... the injection start. During these 120days, the CO2 migrates about 25m in the expected groundwater flow direction. Water electrical conductivity (EC) sampling using small screens in 29 wells allows for very good verification of the ERT results. Water EC and ERT results generally agree very well, with the water...

Arsenic mobilization in a freshening groundwater system formed within glaciomarine deposits

International Nuclear Information System (INIS)

Cavalcanti de Albuquerque, R.; Kirste, D.

2012-01-01

Arsenic release to groundwater and conditions favoring As mobility are investigated in a system of aquifers formed within unconsolidated Quaternary sediments. The studied groundwater system is comprised of unconfined aquifers formed in glaciofluvial sediments with Ca–Mg–HCO 3 groundwater, and confined aquifers formed within glaciomarine sediments with high As (above 10 μg/L) Na–HCO 3 or Na–Cl groundwater. A positive relationship of As concentrations with the Na/(Ca + Mg) ratio of groundwater indicates that As release occurs in glaciomarine sediments concurrent to cation exchange reactions related to groundwater freshening. Arsenic is mobile in confined aquifers as a result of groundwater basic pH which prevents arsenate from adsorbing to mineral surfaces, and reducing conditions that favor speciation to arsenite. Selected extractions applied to sediment core samples indicate that As occurs in sediments predominantly in sulfide minerals and in Mn oxides and/or Fe oxyhydroxides. General positive relationships between As and the reduced species Fe 2+ , NH 3 and dissolved S 2− suggest that As release occurs at increasingly reducing conditions. Despite likely As release via Fe oxyhydroxide reductive dissolution, Fe remains at relatively low concentrations in groundwater (up to 0.37 mg/L) as a result of possible Fe adsorption and Fe reprecipitation as carbonate minerals favored by basic pH and high alkalinity. The presence of S 2− in some samples, a negative relationship between δ 34 S of SO 4 and SO 4 2- concentrations, and a positive relationship between δ 34 S and δ 18 O of SO 4 indicate that groundwater in confined aquifers is undergoing bacterial SO 4 reduction.

Tracking groundwater discharge to a large river using tracers and geophysics.

Science.gov (United States)

Harrington, Glenn A; Gardner, W Payton; Munday, Tim J

2014-01-01

Few studies have investigated large reaches of rivers in which multiple sources of groundwater are responsible for maintaining baseflow. This paper builds upon previous work undertaken along the Fitzroy River, one of the largest perennial river systems in north-western Australia. Synoptic regional-scale sampling of both river water and groundwater for a suite of environmental tracers ((4) He, (87) Sr/(86) Sr, (222) Rn and major ions), and subsequent modeling of tracer behavior in the river, has enabled definition and quantification of groundwater input from at least three different sources. We show unambiguous evidence of both shallow "local" groundwater, possibly recharged to alluvial aquifers beneath the adjacent floodplain during recent high-flow events, and old "regional" groundwater introduced via artesian flow from deep confined aquifers. We also invoke hyporheic exchange and either bank return flow or parafluvial flow to account for background (222) Rn activities and anomalous chloride trends along river reaches where there is no evidence of the local or regional groundwater inputs. Vertical conductivity sections acquired through an airborne electromagnetic (AEM) survey provide insights to the architecture of the aquifers associated with these sources and general groundwater quality characteristics. These data indicate fresh groundwater from about 300 m below ground preferentially discharging to the river, at locations consistent with those inferred from tracer data. The results demonstrate how sampling rivers for multiple environmental tracers of different types-including stable and radioactive isotopes, dissolved gases and major ions-can significantly improve conceptualization of groundwater-surface water interaction processes, particularly when coupled with geophysical techniques in complex hydrogeological settings. © 2013, National Ground Water Association.

Prediction of Groundwater Quality Trends Resulting from Anthropogenic Changes in Southeast Florida.

Science.gov (United States)

Yi, Quanghee; Stewart, Mark

2018-01-01

The effects of surface water flow system changes caused by constructing water-conservation areas and canals in southeast Florida on groundwater quality under the Atlantic Coastal Ridge was investigated with numerical modeling. Water quality data were used to delineate a zone of groundwater with low total dissolved solids (TDS) within the Biscayne aquifer under the ridge. The delineated zone has the following characteristics. Its location generally coincides with an area where the Biscayne aquifer has high transmissivities, corresponds to a high recharge area of the ridge, and underlies a part of the groundwater mound formed under the ridge prior to completion of the canals. This low TDS groundwater appears to be the result of pre-development conditions rather than seepage from the canals constructed after the 1950s. Numerical simulation results indicate that the time for low TDS groundwater under the ridge to reach equilibrium with high TDS surface water in the water-conservation areas and Everglades National Park are approximately 70 and 60 years, respectively. The high TDS groundwater would be restricted to the water-conservation areas and the park due to its slow eastward movement caused by small hydraulic gradients in Rocky Glades and its mixing with the low TDS groundwater under the high-recharge area of the ridge. The flow or physical boundary conditions such as high recharge rates or low hydraulic conductivity layers may affect how the spatial distribution of groundwater quality in an aquifer will change when a groundwater flow system reaches equilibrium with an associated surface water flow system. © 2017, National Ground Water Association.

Determinants of Shallow Groundwater As Variability in Bangladesh

Science.gov (United States)

Radloff, K. A.; Zheng, Y.; Stute, M.; Rahman, M.; Mihajlov, I.; Siu, H.; Huq, M.; Choudhury, I.; Ahmed, K.; van Geen, A.

2010-12-01

Manually operated tube wells that tap into shallow aquifers remain a critical source of untreated drinking water in south Asia and an estimated 37 million people are still exposed to elevated levels of As in Bangladesh(1). This field effort sought to address two questions. What mechanisms control the partitioning of As between groundwater and sediment? How does groundwater transport affect the spatial variability of dissolved As? Understanding the source of groundwater variability is essential for understanding how [As] will change with time, especially as Bangladesh and its water demands develop. Arsenic mobility and transport within the shallow aquifer was investigated at a 0.5 km2 site where [As] increases from conditions measured by spiking freshly collected sediment was remarkably uniform: Kd = 1.5 ± 0.5 L/kg, at 14 of 15 locations. Push- pull tests were used to alter groundwater [As] surrounding a well, without disturbing the sediment. The aquifer responded to the imposed dis-equilibrium by either adsorbing or desorbing As within a few days. These results provide further evidence that groundwater [As] is controlled by As sorption reactions with the sediment that reach equilibrium rapidly compared to the time scale of groundwater flow. A simple reactive-transport model for the site based on the measured partitioning coefficient, Kd, however, supports the notion that the [As] gradient observed reflects the gradual removal of As by groundwater flow over hundreds to thousands of years. The onset of irrigation and industrial pumping at this site has induced a reversal in flow, consequently groundwater now moves from high [As] into low [As] areas. This change could result in rising [As] to levels >50 μg/L in the village within the next few decades. The rapid economic development of Bangladesh could induce similar changes in groundwater flow, and thus As concentrations, elsewhere. This suggests that periodic monitoring of shallow wells low in As within regions of

Stable Isotopes of Dissolved Nitrate and Boron as Indicators of the Origin and Fate of Nitrate Contamination in Groundwater. Results from the Western Po Plain (Northern Italy)

Energy Technology Data Exchange (ETDEWEB)

Sacchi, E. [Dipartimento di Scienze della Terra e dell' Ambiente, Universita di Pavia (Italy); Istituto di Geoscienze e Georisorse, CNR, Pavia (Italy); Delconte, C. A. [Istituto di Geoscienze e Georisorse, CNR (Italy); Dipartimento di Scienze della Terra e dell' Ambiente, Universita di Pavia (Italy); Pennisi, M. [Istituto di Geoscienze e Georisorse, CNR, Pisa (Italy); Allais, E. [ISO4 s.n.c., Torino (Italy)

2013-07-15

Stable isotopes of dissolved nitrates and boron represent a powerful tool, complementary to existing monitoring data, enabling the identification of nitrate sources, the assessment of their relative contribution to nitrate pollution and the quantification of nitrate transport and removal processes. This contribution aims to present groundwater isotope data obtained in an area of 15 000 km{sup 2} of the western Po plain. Nitrate isotope data show that synthetic fertilisers and anthropogenic organic matter are the main sources of contamination. {delta}{sup 11}B allows the discrimination between manure derived and sewage derived contamination. Results indicate that even in agricultural areas, contamination from sewage exists. Samples from the suburban area of Milan, where sewage was considered the most likely source of contamination, show instead a {delta}{sup 11}B typical for cattle manure. This study demonstrates that the attribution of the contamination to a source based solely on present-day land use may lead to inappropriate conclusions. (author)

Use of radiogenic noble gases for dating groundwater

International Nuclear Information System (INIS)

Marine, I.W.

1981-01-01

The accumulation in groundwater of products from the radioactive decay of elements naturally found in rocks offers a potential for measuring the time that the groundwater has been in contact with the rock. This method of dating groundwater has an advantage over using decay products from atmospheric radionuclides in that the amount of decay product becomes greater with increasing age rather than less. Different decay products accumulate at different rates, however, and, thus, have a different potential usefulness in age determinations. The most useful decay product is helium, which is produced from uranium and thorium. The use of argon-40 produced from potassium is limited because it is abundant in meteoric water. Neon, xenon, and krypton can be used, but only with great difficulty because they are produced in extremely small quantities. In general, the potential for error increases when a long time is required to produce a small quantity of the dating nuclide. An example is given of the use of helium dissolved in groundwater to obtain an age of 840,000 y for water in crystalline metamorphic rock beneath the Savannah River Plant near Aiken, SC. Combined with other information, this water age can be used to measure the hydraulic conductivity of a large mass of rock (tens of kilometers in length). The hydraulic conductivity so calculated compares favorably with that obtained from hydraulic tests

Flood-controlled excess-air formation favors aerobic respiration and limits denitrification activity in riparian groundwater

Directory of Open Access Journals (Sweden)

Simone ePeter

2015-11-01

Full Text Available The saturated riparian zones of rivers act as spatially and temporally variable biogeochemical reactors. This complicates the assessment of biogeochemical transport and transformation processes. During a flood event, excess-air formation, i.e. the inclusion and dissolution of air bubbles into groundwater, can introduce high amounts of dissolved O2 and thereby affect biogeochemical processes in groundwater. With the help of a field-installed membrane-inlet mass-spectrometer we resolved the effects of flood induced excess-air formationon organic carbon and nitrogen transformations in groundwater of different riparian zones of a restored section of the River Thur, Switzerland. The results show that the flood event triggered high aerobic respiration activity in the groundwater below a zone densely populated with willow plants. The flood introduced high concentrations of O2 (230 µmol L–1 to the groundwater through the formation of excess air and transported up to ~400 µmol L 1 organic carbon from the soil/root layer into groundwater during the movement of the water table. A rapid respiration process, quantified via the measurements of O2, CO2 and noble-gas concentrations, led to fast depletion of the introduced O2 and organic carbon and to high CO2 concentration (590 µmol L–1 in the groundwater shortly after the flood. The synchronous analysis of different nitrogen species allowed studying the importance of denitrification activity. The results indicate that in the willow zone excess-air formation inhibited denitrification through high O2 concentration input. Instead, the observed decrease in nitrate concentration (~50 µmol N L 1 may be related to fostered nitrate uptake by plants. In the other riparian zones closer to the river, no significant excess-air formation and corresponding respiration activity was observed. Overall, analyzing the dissolved gases in the groundwater significantly contributed to deciphering biogeochemical processes in

Relationship of Shallow Groundwater Quality to Hydraulic Fracturing Activities in Antrim and Kalkaska Counties, MI

Science.gov (United States)

Stefansky, J. N.; Robertson, W. M.; Chappaz, A.; Babos, H.; Israel, S.; Groskreutz, L. M.

2015-12-01

Hydraulic fracturing (fracking) of oil and natural gas (O&G) wells is a widely applied technology that can increase yields from tight geologic formations. However, it is unclear how fracking may impact shallow groundwater; previous research into its effects has produced conflicting results. Much of the worry over potential impacts to water quality arises from concerns about the produced water. The water produced from O&G formations is often salty, contains toxic dissolved elements, and can be radioactive. If fracking activities cause or increase connectivity between O&G formations and overlying groundwater, there may be risks to aquifers. As one part of a groundwater quality study in Antrim and Kalkaska Counties, MI, samples were collected from the unconfined glacial aquifer (3-300 m thick) and produced water from the underlying Antrim formation, a shallow (180-670 m deep) natural gas producing black shale. Groundwater samples were collected between 200 to 10,000 m distance from producing Antrim gas wells and from a range of screened intervals (15-95 m). Samples were analyzed for major constituents (e.g., Br, Cl), pH, conductivity, and dissolved oxygen (DO). The specific conductance of groundwater samples ranged from 230-1020 μS/cm; DO ranged from 0.4-100% saturation. Preliminary results show a slight inverse correlation between specific conductance and proximity to producing Antrim wells. The observed range of DO saturation in glacial aquifer groundwater appears to be related to both screened depth of the water wells and proximity to Antrim wells. During sampling, some well owners expressed concerns about the effects of fracking on groundwater quality and reported odd smells and tastes in their water after O&G drilling occurred near their homes. The results of this study and reported observations provide evidence to suggest a potential hydrogeological connection between the Antrim formation and the overlying glacial aquifer in some locations; it also raises

Radon as a natural geochemical tracer for study of groundwater discharge into lakes

International Nuclear Information System (INIS)

Schmidt, Axel

2008-01-01

In the presented work the suitability of the naturally occurring radioactive noble gas isotope radon-222 for qualitative and quantitative description of groundwater discharge into lakes was studied. Basis of these investigations was the development of two innovative techniques for the on-site determination of radon in water. In the ex-situ radon measurement procedure, water from the source concerned is taken up in an exchange cell used for this purpose. Inside this cell, the radon dissolved in water is transferred via diffusion into a closed counter-flow of air and subsequently detected by a radon-in-air monitor. Where the in-situ radon determination is concerned, a module composed of a semipermeable membrane is introduced into a water column. Subsequently, the radon dissolved in the water body diffuses through the membrane into the corresponding air flow, by means of which it is transferred into a radon-in-air monitor and is detected. Combination of the developed mobile radon extraction techniques with a suitable and portable radon monitor allow the detection of radon-222 with sufficient accuracy (smaller 20 %) in groundwater as well as in surface waters, i.e., within a broad range of concentrations. Radon-222 was subsequently used to characterize groundwater discharge into a meromictic and a dimictic lake, i.e. two types of lake basically distinct from each other with respect to their water circulation properties were investigated. The use of the noble gas isotope radon-222 as a geochemical tracer makes the application of on-site detection techniques possible and that this in turn permits a rapid, reliable, and cost-effective assessment of groundwater discharge rates into lake water bodies

Radon as a natural geochemical tracer for study of groundwater discharge into lakes

Energy Technology Data Exchange (ETDEWEB)

Schmidt, Axel

2008-06-27

In the presented work the suitability of the naturally occurring radioactive noble gas isotope radon-222 for qualitative and quantitative description of groundwater discharge into lakes was studied. Basis of these investigations was the development of two innovative techniques for the on-site determination of radon in water. In the ex-situ radon measurement procedure, water from the source concerned is taken up in an exchange cell used for this purpose. Inside this cell, the radon dissolved in water is transferred via diffusion into a closed counter-flow of air and subsequently detected by a radon-in-air monitor. Where the in-situ radon determination is concerned, a module composed of a semipermeable membrane is introduced into a water column. Subsequently, the radon dissolved in the water body diffuses through the membrane into the corresponding air flow, by means of which it is transferred into a radon-in-air monitor and is detected. Combination of the developed mobile radon extraction techniques with a suitable and portable radon monitor allow the detection of radon-222 with sufficient accuracy (smaller 20 %) in groundwater as well as in surface waters, i.e., within a broad range of concentrations. Radon-222 was subsequently used to characterize groundwater discharge into a meromictic and a dimictic lake, i.e. two types of lake basically distinct from each other with respect to their water circulation properties were investigated. The use of the noble gas isotope radon-222 as a geochemical tracer makes the application of on-site detection techniques possible and that this in turn permits a rapid, reliable, and cost-effective assessment of groundwater discharge rates into lake water bodies.

The survey reasarch about groundwater in a mine making use of the sour method to immerse at originl place in Xinjiang province

International Nuclear Information System (INIS)

Xu Yiqun; Yang Yihan

2014-01-01

Basing on a mine making use of a sour method to immerse at original place in Xiniang province, building up a monitor network of mine and its Surroundings groundwater, by the mispreads experiment at the spot and the Earth physical method to mointer Pollute scope and imitate the flow of groundwater and the movement of dissolve quality. Making use of the method speaking of to investigate groundwater in mineral layer completely. According to the investigating result, Comparing the original date of groundwater in mineral layer and the national Quality standard of groundwater to evaluate the present Pollute condition of groundwater existmg in the A # , B # mine ore aquifer. This studies Proves that Pollution mainly exists in the A # , B # mine ore aquifer and its surrounding limited area, groundwater upper or lower the ore aquifer is not affected by pollution. (authors)

Groundwater-quality data in the Western San Joaquin Valley study unit, 2010 - Results from the California GAMA Program

Science.gov (United States)

Mathany, Timothy M.; Landon, Matthew K.; Shelton, Jennifer L.; Belitz, Kenneth

2013-01-01

), constituents of special interest (perchlorate, N-nitrosodimethylamine [NDMA], and 1,2,3-trichloropropane [1,2,3-TCP]), and naturally occurring inorganic constituents (trace elements, nutrients, dissolved organic carbon [DOC], major and minor ions, silica, total dissolved solids [TDS], alkalinity, total arsenic and iron [unfiltered] and arsenic, chromium, and iron species [filtered]). Isotopic tracers (stable isotopes of hydrogen, oxygen, and boron in water, stable isotopes of nitrogen and oxygen in dissolved nitrate, stable isotopes of sulfur in dissolved sulfate, isotopic ratios of strontium in water, stable isotopes of carbon in dissolved inorganic carbon, activities of tritium, and carbon-14 abundance), dissolved standard gases (methane, carbon dioxide, nitrogen, oxygen, and argon), and dissolved noble gases (argon, helium-4, krypton, neon, and xenon) were measured to help identify sources and ages of sampled groundwater. In total, 245 constituents and 8 water-quality indicators were measured. Quality-control samples (blanks, replicates, or matrix spikes) were collected at 16 percent of the wells in the WSJV study unit, and the results for these samples were used to evaluate the quality of the data from the groundwater samples. Blanks rarely contained detectable concentrations of any constituent, suggesting that contamination from sample collection procedures was not a significant source of bias in the data for the groundwater samples. Replicate samples all were within acceptable limits of variability. Matrix-spike recoveries were within the acceptable range (70 to 130 percent) for approximately 87 percent of the compounds. This study did not evaluate the quality of water delivered to consumers. After withdrawal, groundwater typically is treated, disinfected, and (or) blended with other waters to maintain water quality. Regulatory benchmarks apply to water that is delivered to the consumer, not to untreated groundwater. However, to provide some context for the results

Speciation and mobility of trace elements and uranium in a river/groundwater infiltration system

International Nuclear Information System (INIS)

Gunten, H.R. von

1994-01-01

The infiltration and migration behaviour of dissolved species from the river Glatt, Switzerland, into a hydrologically connected shallow groundwater aquifer was investigated for more than 10 years. Seasonal cycles of the concentrations of several species were observed in the sediments of the riverbed and in the groundwater. The bacteria-mediated oxidation of organic matter and aquatic biota in the riverbed sediments governed related chemical and redox processes which led to significant changes in the composition and properties of the infiltrating water. Up to 1990, significant peaks of manganese, cadmium, uranium and other trace elements appeared each summer in the interstitial water of the sediments and in the groundwater. Recently, these peaks disappeared completely. The authors attribute these drastic changes in the water chemistry to a more efficient removal of the nutrient phosphate from surface waters

Isotope geochemistry of sulfur in forest soils and in new groundwater below forest soils

International Nuclear Information System (INIS)

Mayer, B.

1993-04-01

The isotope geochemistry of sulphur in aerobic forest soils and new groundwater below forest soils was investigated for the purpose of investigating the transport and transformation behaviour of sulfate in the water-unsaturated zone. The effects of hydrodynamic and biogeochemical processes on the development of seepage water sulfate isotopes between depositions and groundwater were investigated by means of laboratory experiments, profile studies, lysimeter experiments, and field studies in order to determine the sulphur conversion processes. Dissolved sulphur from precipitates, seepage water, creek water and groundwater, as well as sulphur extracted from soil samples, were precipitated in the form of BaSO 4 or AgS 2 , decomposed thermally into SO 2 or CO 2 , and the 34 S/ 32 S and 18 O/ 16 O isotope ratios were determined by mass spectrometry. (orig.) [de

The Effect of CO2 on Partial Reactive Crystallization of MORB-Eclogite-derived Basaltic Andesite in Peridotite and Generation of Silica-Undersaturated Basalts

Science.gov (United States)

Mallik, A.; Dasgupta, R.

2012-12-01

Recycled oceanic crust (MORB-eclogite) is considered to be the dominant heterogeneity in Earth's mantle. Because MORB-eclogite is more fusible than peridotite, siliceous partial melt derived from it must react with peridotite while the latter is still in the subsolidus state. Thus, studying such reactive process is important in understanding melting dynamics of the Earth's mantle. Reaction of MORB-eclogite-derived andesitic partial melt with peridotite can produce alkalic melts by partial reactive crystallization but these melts are not as silica-undersaturated as many natural basanites, nephelinites or melititites [1]. In this study, we constrain how dissolved CO2 in a siliceous MORB-eclogite-derived partial melt affects the reaction phase equilibria involving peridotite and can produce nephelinitic melts. Here we compare experiments on CO2-free [1] and 2.6 wt.% CO2 bearing andesitic melt+lherzolite mixtures conducted at 1375 °C and 3 GPa with added melt fraction of 8-50 wt.%. In both CO2-free and CO2-bearing experiments, melt and olivine are consumed and opx and garnet are produced, with the extent of modal change for a given melt-rock ratio being greater for the CO2-bearing experiments. While the residue evolves to a garnet websterite by adding 40% of CO2-bearing melt, the residue becomes olivine-free by adding 50% of the CO2-free melt. Opx mode increases from 12 to ~55 wt.% for 0 to 40% melt addition in CO2-bearing system and 12 to ~43 wt.% for 0 to 50% melt addition in CO2-free system. Garnet mode, for a similar range of melt-rock ratio, increases from ~10 to ~15 wt.% for CO2 bearing system and to ~11 wt.% for CO2-free system. Reacted melts from 25-33% of CO2-bearing melt-added runs contain ~39 wt.% SiO2 , ~11-13 wt.% TiO2, ~9 wt.% Al2O3, ~11 wt.% FeO*, 16 wt.% MgO, 10-11 wt.% CaO, and 3 wt.% Na2O whereas experiments with a similar melt-rock ratio in a CO2-free system yield melts with 44-45 wt.% SiO2, 6-7 wt.% TiO2, 13-14 wt.% Al2O3, 10-11 wt.% FeO*, 12-13 wt

The role of alluvial aquifer sediments in attenuating a dissolved arsenic plume.

Science.gov (United States)

Ziegler, Brady A; Schreiber, Madeline E; Cozzarelli, Isabelle M

2017-09-01

In a crude-oil-contaminated sandy aquifer at the Bemidji site in northern Minnesota, biodegradation of petroleum hydrocarbons has resulted in release of naturally occurring As to groundwater under Fe-reducing conditions. This study used chemical extractions of aquifer sediments collected in 1993 and 2011-2014 to evaluate the relationship between Fe and As in different redox zones (oxic, methanogenic, Fe-reducing, anoxic-suboxic transition) of the contaminated aquifer over a twenty-year period. Results show that 1) the aquifer has the capacity to naturally attenuate the plume of dissolved As, primarily through sorption; 2) Fe and As are linearly correlated in sediment across all redox zones, and a regression analysis between Fe and As reasonably predicted As concentrations in sediment from 1993 using only Fe concentrations; 3) an As-rich "iron curtain," associated with the anoxic-suboxic transition zone, migrated 30m downgradient between 1993 and 2013 as a result of the hydrocarbon plume evolution; and 4) silt lenses in the aquifer preferentially sequester dissolved As, though As is remobilized into groundwater from sediment after reducing conditions are established. Using results of this study coupled with historical data, we develop a conceptual model which summarizes the natural attenuation of As and Fe over time and space that can be applied to other sites that experience As mobilization due to an influx of bioavailable organic matter. Copyright © 2017 Elsevier B.V. All rights reserved.

The role of alluvial aquifer sediments in attenuating a dissolved arsenic plume

Science.gov (United States)

Ziegler, Brady A.; Schreiber, Madeline E.; Cozzarelli, Isabelle M.

2017-01-01

In a crude-oil-contaminated sandy aquifer at the Bemidji site in northern Minnesota, biodegradation of petroleum hydrocarbons has resulted in release of naturally occurring As to groundwater under Fe-reducing conditions. This study used chemical extractions of aquifer sediments collected in 1993 and 2011–2014 to evaluate the relationship between Fe and As in different redox zones (oxic, methanogenic, Fe-reducing, anoxic-suboxic transition) of the contaminated aquifer over a twenty-year period. Results show that 1) the aquifer has the capacity to naturally attenuate the plume of dissolved As, primarily through sorption; 2) Fe and As are linearly correlated in sediment across all redox zones, and a regression analysis between Fe and As reasonably predicted As concentrations in sediment from 1993 using only Fe concentrations; 3) an As-rich “iron curtain,” associated with the anoxic-suboxic transition zone, migrated 30 m downgradient between 1993 and 2013 as a result of the hydrocarbon plume evolution; and 4) silt lenses in the aquifer preferentially sequester dissolved As, though As is remobilized into groundwater from sediment after reducing conditions are established. Using results of this study coupled with historical data, we develop a conceptual model which summarizes the natural attenuation of As and Fe over time and space that can be applied to other sites that experience As mobilization due to an influx of bioavailable organic matter.

Groundwater geochemistry and its implications for arsenic mobilization in shallow aquifers of the Hetao Basin, Inner Mongolia

International Nuclear Information System (INIS)

Guo Huaming; Yang Suzhen; Tang Xiaohui; Li Yuan; Shen Zhaoli

2008-01-01

Arsenic concentrations in shallow groundwaters from the Hetao Basin of Inner Mongolia range between 0.6 and 572 μg/L. High As groundwaters generally occur in the shallow alluvial-lacustrine aquifers, which are mainly composed of black (or dark grey) fine sands in a reducing environment. They are characterized by high concentrations of dissolved Fe, Mn, HCO 3 - , P and S 2- , and low concentrations of NO 3 - and SO 4 2- . Low SO 4 2- coupled with high S 2- suggests that SO 4 2- reduction has been an active process. In the reducing groundwaters, inorganic As(III) accounts for around 75% of total dissolved As. Total As contents in the sediments from three representative boreholes are observed to be 7.3-73.3 mg/kg (average of 18.9 mg/kg). The total As is mildly-strongly correlated with total Fe and total Mn, while a quite weak correlation exists between total As and total S, suggesting that the As is associated with Fe-Mn oxides, rather than sulfides in the sediments. It is found in the sequential extraction that chemically active As is mainly bound to Fe-Mn oxides, up to 3500 μg/kg. The mobilization of As under reducing conditions is believed to include reductive dissolution of Fe-Mn oxides and reduction of adsorbed As. Although exchangeable As is labile and very vulnerable to hydrogeochemical condition, the contribution is relatively limited due to the low concentrations. The competition between As and other anions (such as HPO 4 2- ) for binding sites on Fe-Mn oxides may also give rise to the release of As into groundwater. Slow groundwater movement helps accumulation of the released As in the groundwaters

Biogeochemical transport in the Loxahatchee River estuary, FL: The role of submarine groundwater discharge

Science.gov (United States)

Swarzenski, P.; Orem, B.; McPherson, B.; Baskaran, M.; Wan, Y.

2005-05-01

The distributions of dissolved organic carbon (DOC), silica, select trace elements (Mn, Fe, Ba, Sr, Co, V,) and a suite of naturally-occurring radionuclides in the U/Th decay series (222Rn, 223,224,226,228Ra, 238U) were studied during high and low discharge conditions in the Loxahatchee River estuary, Florida. The zero-salinity endmember of this still relatively pristine estuary may reflect not only river-borne constituents, but also those advected during active groundwater/surface-water discharge. During low discharge conditions, with the notable exception of Co, trace metals indicate nearly conservative mixing from a salinity of ~12 through the estuary (This statement contracdicts with what is said in p. 7). In contrast, of the trace metals studied, only Sr, Fe, U and V exhibited conservative estuarine mixing during high discharge. Dissolved organic carbon and Si concentrations were highest at zero salinities, and generally decreased with an increase in salinity during both discharge regimes, indicating removal of land-derived dissolved organic matter and silica in the estuary. Suspended particulate matter (SPM) concentrations were generally lowest ( 28 dpm L-1) at the freshwater endmember of the estuary, and appear to identify regions of the river most influenced by active submarine groundwater discharge (where is the data that show this?). Activities of four naturally-occurring isotopes of Ra (223,224,226,228Ra) in this estuary and select adjacent shallow groundwater wells indicate mean estuarine water mass residence times of less than 1 day; values in close agreement to those calculated by tidal prism and tidal period. A radium-based model for estimating submarine groundwater discharge to the Loxahatchee River estuary yielded an average of 1.03 V 3.84 x 105 m3 day-1, depending on river discharge stage as well as slight variations in the particular Ra models used. Such calculated flux estimates are in close agreement with results obtained from a 2-day

Natural radioactivity in groundwater from the south-eastern Arabian Peninsula and environmental implications.

Science.gov (United States)

Murad, A; Zhou, X D; Yi, P; Alshamsi, D; Aldahan, A; Hou, X L; Yu, Z B

2014-10-01

Groundwater is the most valuable resource in arid regions, and recognizing radiological criteria among other water quality parameters is essential for sustainable use. In the investigation presented here, gross-α and gross-β were measured in groundwater samples collected in the south-eastern Arabian Peninsula, 67 wells in Unite Arab Emirates (UAE), as well as two wells and one spring in Oman. The results show a wide gross-α and gross-β activities range in the groundwater samples that vary at 0.01∼19.5 Bq/l and 0.13∼6.6 Bq/l, respectively. The data show gross-β and gross-α values below the WHO permissible limits for drinking water in the majority of the investigated samples except those in region 4 (Jabel Hafit and surroundings). No correlation between groundwater pH and the gross-α and gross-β, while high temperatures probably enhance leaching of radionuclides from the aquifer body and thereby increase the radioactivity in the groundwater. This conclusion is also supported by the positive correlation between radioactivity and amount of total dissolved solid. Particular water purification technology and environmental impact assessments are essential for sustainable and secure use of the groundwater in regions that show radioactivity values far above the WHO permissible limit for drinking water.

Experiences of Mass Pig Carcass Disposal Related to Groundwater Quality Monitoring in Taiwan

Directory of Open Access Journals (Sweden)

Zeng-Yei Hseu

2016-12-01

Full Text Available The pig industry is the most crucial animal industry in Taiwan; 10.7 million pigs were reared for consumption in 1996. A foot and mouth disease (FMD epidemic broke out on 19 March 1997, and 3,850,536 pigs were culled before July in the same year. The major disposal method of pig carcasses from the FMD outbreak was burial, followed by burning and incineration. To investigate groundwater quality, environmental monitoring of burial sites was performed from October 1997 to June 1999; groundwater monitoring of 90–777 wells in 20 prefectures was performed wo to six times in 1998. Taiwanese governmental agencies analyzed 3723 groundwater samples using a budget of US $1.5 million. The total bacterial count, fecal coliform, Salmonella spp., nitrite-N, nitrate-N, ammonium-N, sulfate, non-purgeable organic carbon, total oil, and total dissolved solid were recognized as indicators of groundwater contamination resulting from pig carcass burial. Groundwater at the burial sites was considered to be contaminated on the basis of the aforementioned indicators, particularly groundwater at burial sites without an impermeable cloth and those located at a relatively short distance from the monitoring well. The burial sites selected during outbreaks in Taiwan should have a low surrounding population, be away from water preservation areas, and undergo regular monitoring of groundwater quality.

Isotopic study of the effect of Tarbela reservoir on the groundwater system in the downstream areas

International Nuclear Information System (INIS)

Sajjad, M.I.; Tasneem, M.A.; Hussain, S.D.; Khan, I.H.; Ali, M.; Latif, Z.

1994-04-01

Isotopic studies were carried out on the right side of river Indus, downstream of Tarbela dam to study the effect of Tarbela Reservoir on the groundwater system. The main objectives of the study were to determine the hydraulic connection, if any, between the Tarbela Lake and the groundwater appearing in the ponds near Gadon Amazai, see the effect of Tarbela dam on the groundwater system in the downstream areas, compute the relative contribution of different recharge sources towards groundwater system and to estimate residence time of groundwater in the area. Isotopic data reveals that the ponds near Gadoon Amazai area are being recharged by local rains and there is no contribution of Tarbela lake. The area around Gadoon Amazai, Topi and Kalabat is solely recharged by local rains while the area around Swabi, Zaida and Lahor has mixed recharge with major contribution from local canal system. Tritium data suggests that the residence time of groundwater in the study area varies from a few years to 30 years. Te groundwater in the area has low dissolved salt contents and is, generally, of good quality. (author) 19 figs

Influences of groundwater extraction on flow dynamics and arsenic levels in the western Hetao Basin, Inner Mongolia, China

Science.gov (United States)

Zhang, Zhuo; Guo, Huaming; Zhao, Weiguang; Liu, Shuai; Cao, Yongsheng; Jia, Yongfeng

2018-04-01

Data on spatiotemporal variations in groundwater levels are crucial for understanding arsenic (As) behavior and dynamics in groundwater systems. Little is known about the influences of groundwater extraction on the transport and mobilization of As in the Hetao Basin, Inner Mongolia (China), so groundwater levels were recorded in five monitoring wells from 2011 to 2016 and in 57 irrigation wells and two multilevel wells in 2016. Results showed that groundwater level in the groundwater irrigation area had two troughs each year, induced by extensive groundwater extraction, while groundwater levels in the river-diverted (Yellow River) water irrigation area had two peaks each year, resulting from surface-water irrigation. From 2011 to 2016, groundwater levels in the groundwater irrigation area presented a decreasing trend due to the overextraction. Groundwater samples were taken for geochemical analysis each year in July from 2011 to 2016. Increasing trends were observed in groundwater total dissolved solids (TDS) and As. Owing to the reverse groundwater flow direction, the Shahai Lake acts as a new groundwater recharge source. Lake water had flushed the near-surface sediments, which contain abundant soluble components, and increased groundwater salinity. In addition, groundwater extraction induced strong downward hydraulic gradients, which led to leakage recharge from shallow high-TDS groundwater to the deep semiconfined aquifer. The most plausible explanation for similar variations among As, Fe(II) and total organic carbon (TOC) concentrations is the expected dissimilatory reduction of Fe(III) oxyhydroxides.

Measuring the pollutant transport capacity of dissolved organic matter in complex matrixes

DEFF Research Database (Denmark)

Persson, L.; Alsberg, T.; Odham, G.

2003-01-01

Dissolved organic matter (DOM) facilitated transport in contaminated groundwater was investigated through the measurement of the binding capacity of landfill leachate DOM (Vejen, Denmark) towards two model pollutants (pyrene and phenanthrene). Three different methods for measuring binding capacity....... It was further concluded that DOM facilitated transport should be taken into account for non-ionic PAHs with lg K OW above 5, at DOM concentrations above 250 mg C/L. The total DOM concentration was found to be more important for the potential of facilitated transport than differences in the DOM binding capacity....

Source and distribution of naturally occurring arsenic in groundwater from Alberta’s Southern Oil Sands Regions

International Nuclear Information System (INIS)

Moncur, Michael C.; Paktunc, Dogan; Jean Birks, S.; Ptacek, Carol J.; Welsh, Brent; Thibault, Yves

2015-01-01

Highlights: • Widespread naturally occurring As in groundwater with concentrations up to 179 μg/L. • 50% of the 816 water wells sampled exceeded 10 μg/L of As. • As(III) was the dominant species in 74% of the groundwater samples. • Shallow groundwater As is derived from arsenian pyrite oxidation. • In deeper sediments, As release is associated with Fe(III) reduction. - Abstract: Arsenic (As) concentrations as high as 179 μg/L have been observed in shallow groundwater in the Alberta’s Southern Oil Sand Regions. The geology of this area of Alberta includes a thick cover (up to 200 m) of unconsolidated glacial deposits, with a number of regional interglacial sand and gravel aquifers, underlain by marine shale. Arsenic concentrations observed in 216 unconsolidated sediment samples ranged from 1 and 17 ppm. A survey of over 800 water wells sampled for As in the area found that 50% of the wells contained As concentrations exceeding drinking water guidelines of 10 μg/L. Higher As concentrations in groundwater were associated with reducing conditions. Measurements of As speciation from 175 groundwater samples indicate that As(III) was the dominant species in 74% of the wells. Speciation model calculations showed that the majority of groundwater samples were undersaturated with respect to ferrihydrite, suggesting that reductive dissolution of Fe-oxyhydroxides may be the source of some As in groundwater. Detailed mineralogical characterization of sediment samples collected from two formations revealed the presence of fresh framboidal pyrite in the deeper unoxidized sediments. Electron microprobe analysis employing wavelength dispersive spectrometry indicated that the framboidal pyrite had variable As content with an average As concentration of 530 ppm, reaching up to 1840 ppm. In contrast, the oxidized sediments did not contain framboidal pyrite, but exhibited spheroidal Fe-oxyhydroxide grains with elevated As concentrations. The habit and composition suggest

Use of environmental isotopes for studying human induced change in groundwater environment in Lahore, Pakistan

International Nuclear Information System (INIS)

Ahmad, M.; Akram, W.; Sajjad, M.I.; Rafiq, M.; Tasneem, Azam M.

2002-01-01

Lahore is the second biggest city of Pakistan where groundwater is the only source of drinking water supply for the city. On the other hand, the quality of groundwater is being degraded due to various human activities especially due to waste disposal practices. Untreated domestic and industrial wastes are discharged into open channels, drains, etc. which leads to surface water and groundwater pollution. This study was undertaken to assess the changes in groundwater environment due to such activities. Water samples were collected on periodical basis from existing handpumps, tube wells and drains and analyzed for isotopic ( 2 H, 3 H, 13 C, 18 O) and major dissolved ions. Samples having high nitrate were analyzed for 15 N. Selected samples were also analyzed for Coliform bacteria. Results of only selected parameters are discussed here. The data showed that quality of shallow groundwater has deteriorated at most of the locations and concentrations of several chemical parameters are higher than WHO permissible levels for drinking water. Comparison with a previous study carried out in 1991, indicated a clear increasing trend of total dissolved salts in groundwater. An outstanding feature of the data is the increasing trend of nitrate concentrations both in shallow and deep groundwater. Results of nitrate analysis indicate that concentrations vary from 10 to 188 mg/l in shallow groundwater and 9 to 41 mg/l in deep groundwater. Frequency histogram of nitrate concentrations is shown. Nitrates which were generally a few ppm have increased at almost all the surveyed locations and have even crossed the WHO limit of 45 mg/l at several shallow locations. High nitrate waters exist as isolated pockets. Results of tritium analysis indicated that shallow groundwater has generally high tritium values. Presence of more nitrate at shallow depths, occurrence of high nitrate waters as isolated pockets and high tritium in contaminated waters suggest that nitrates are derived from as

Depth Stratification Leads to Distinct Zones of Manganese and Arsenic Contaminated Groundwater.

Science.gov (United States)

Ying, Samantha C; Schaefer, Michael V; Cock-Esteb, Alicea; Li, Jun; Fendorf, Scott

2017-08-15

Providing access to safe drinking water is a global challenge, for which groundwater is increasingly being used throughout the world. However, geogenic contaminants limit the suitability of groundwater for domestic purposes over large geographic areas across most continents. Geogenic contaminants in groundwater are often evaluated individually, but here we demonstrate the need to evaluate multiple contaminants to ensure that groundwater is safe for human consumption and agricultural usage. We compiled groundwater chemical data from three aquifer regions across the world that have been reported to have widespread As and Mn contamination including the Glacial Aquifer in the U.S., the Ganges-Brahmaputra-Mehta Basin within Bangladesh, and the Mekong Delta in Cambodia, along with newly sampled wells in the Yangtze River Basin of China. The proportion of contaminated wells increase by up to 40% in some cases when both As and Mn contaminants are considered. Wilcoxon rank-sum analysis indicates that Mn contamination consistently occurs at significantly shallower depths than As contaminated wells in all regions. Arsenic concentrations in groundwater are well predicted by redox indicators (Eh and dissolved oxygen) whereas Mn shows no significant relationship with either parameter. These findings illustrate that the number of safe wells may be drastically overestimated in some regions when Mn contamination is not taken into account and that depth may be used as a distinguishing variable in efforts to predict the presence of groundwater contaminants regionally.

Organic carbon input in shallow groundwater at Aspo, southeastern Sweden

International Nuclear Information System (INIS)

Wallin, B.

1993-01-01

The variation in carbon and oxygen isotopes in calcite fissure fillings and dissolved carbonate from shallow groundwaters has been examined at Aspo, southeastern Sweden. The shallow water lens is refilled by meteoric water and is considered as an open system. The σ 13 C-signatures of the dissolved carbonate fall within a narrow range of -15.8 to -17.4 per-thousand, indicative of organic an organic carbon source. The low σ 13 C-values suggest that input of soil-CO 2 is the dominating carbon source for the system. σ 13 C and σ 18 O-values in the calcite fissure fillings show a wide range in values with a possible two end-member mixing of early post glacial atmospheric CO 2 dominated system to a present day soil-CO 2 dominating carbon source

In situ treatment of cyanide-contaminated groundwater by iron cyanide precipitation

International Nuclear Information System (INIS)

Ghosh, R.S.; Dzombak, D.A.; Luthy, R.G.; Smith, J.R.

1999-01-01

Groundwater contamination with cyanide is common at many former or active industrial sites. Metal-cyanide complexes typically dominate aqueous speciation of cyanide in groundwater systems, with iron-cyanide complexes often most abundant. Typically, metal-cyanide complexes behave as nonadsorbing solutes in sand-gravel aquifer systems in the neutral pH range, rendering cyanide relatively mobile in groundwater systems. Groundwater pump-and-treat systems have often been used to manage cyanide contamination in groundwater. This study examined the feasibility of using in situ precipitation of iron cyanide in a reactive barrier to attenuate the movement of cyanide in groundwater. Laboratory column experiments were performed in which cyanide solutions were passed through mixtures of sand and elemental iron filings. Removal of dissolved cyanide was evaluated in a variety of cyanide-containing influents under various flow rates and sand-to-iron weight ratios. Long-term column tests performed with various cyanide-containing influents under both oxic and anoxic conditions, at neutral pH and at flow rates typical of sand-gravel porous media, yielded effluent concentrations of total cyanide as low as 0.5 mg/L. Effluent cyanide concentrations achieved were close to the solubilities of Turnbull's blue-hydrous ferric oxide solid solutions, indicating co-precipitation of the two solids. Maximum cyanide removal efficiency was achieved with approximately 10% by weight of iron in the sand-iron mixtures; higher iron contents did not increase removal efficiency significantly. Results obtained indicate that in situ precipitation is a promising passive treatment approach for cyanide in groundwater

Geochemistry of groundwater in the eastern Snake River Plain aquifer, Idaho National Laboratory and vicinity, eastern Idaho

Science.gov (United States)

Rattray, Gordon W.

2018-05-30

Nuclear research activities at the U.S. Department of Energy (DOE) Idaho National Laboratory (INL) in eastern Idaho produced radiochemical and chemical wastes that were discharged to the subsurface, resulting in detectable concentrations of some waste constituents in the eastern Snake River Plain (ESRP) aquifer. These waste constituents may pose risks to the water quality of the aquifer. In order to understand these risks to water quality the U.S. Geological Survey, in cooperation with the DOE, conducted a study of groundwater geochemistry to improve the understanding of hydrologic and chemical processes in the ESRP aquifer at and near the INL and to understand how these processes affect waste constituents in the aquifer.Geochemistry data were used to identify sources of recharge, mixing of water, and directions of groundwater flow in the ESRP aquifer at the INL. The geochemistry data were analyzed from 167 sample sites at and near the INL. The sites included 150 groundwater, 13 surface-water, and 4 geothermal-water sites. The data were collected between 1952 and 2012, although most data collected at the INL were collected from 1989 to 1996. Water samples were analyzed for all or most of the following: field parameters, dissolved gases, major ions, dissolved metals, isotope ratios, and environmental tracers.Sources of recharge identified at the INL were regional groundwater, groundwater from the Little Lost River (LLR) and Birch Creek (BC) valleys, groundwater from the Lost River Range, geothermal water, and surface water from the Big Lost River (BLR), LLR, and BC. Recharge from the BLR that may have occurred during the last glacial epoch, or paleorecharge, may be present at several wells in the southwestern part of the INL. Mixing of water at the INL primarily included mixing of surface water with groundwater from the tributary valleys and mixing of geothermal water with regional groundwater. Additionally, a zone of mixing between tributary valley water and

Quality of groundwater and surface water, Wood River Valley, south-central Idaho, July and August 2012

Science.gov (United States)

Hopkins, Candice B.; Bartolino, James R.

2013-01-01

Residents and resource managers of the Wood River Valley of south-central Idaho are concerned about the effects that population growth might have on the quality of groundwater and surface water. As part of a multi-phase assessment of the groundwater resources in the study area, the U.S. Geological Survey evaluated the quality of water at 45 groundwater and 5 surface-water sites throughout the Wood River Valley during July and August 2012. Water samples were analyzed for field parameters (temperature, pH, specific conductance, dissolved oxygen, and alkalinity), major ions, boron, iron, manganese, nutrients, and Escherichia coli (E.coli) and total coliform bacteria. This study was conducted to determine baseline water quality throughout the Wood River Valley, with special emphasis on nutrient concentrations. Water quality in most samples collected did not exceed U.S. Environmental Protection Agency standards for drinking water. E. coli bacteria, used as indicators of water quality, were detected in all five surface-water samples and in two groundwater samples collected. Some analytes have aesthetic-based recommended drinking water standards; one groundwater sample exceeded recommended iron concentrations. Nitrate plus nitrite concentrations varied, but tended to be higher near population centers and in agricultural areas than in tributaries and less populated areas. These higher nitrate plus nitrite concentrations were not correlated with boron concentrations or the presence of bacteria, common indicators of sources of nutrients to water. None of the samples collected exceeded drinking-water standards for nitrate or nitrite. The concentration of total dissolved solids varied considerably in the waters sampled; however a calcium-magnesium-bicarbonate water type was dominant (43 out of 50 samples) in both the groundwater and surface water. Three constituents that may be influenced by anthropogenic activity (chloride, boron, and nitrate plus nitrite) deviate from this

Groundwater-quality data in the Klamath Mountains study unit, 2010: results from the California GAMA Program

Science.gov (United States)

Mathany, Timothy M.; Belitz, Kenneth

2014-01-01

Groundwater quality in the 8,806-square-mile Klamath Mountains (KLAM) study unit was investigated by the U.S. Geological Survey (USGS) from October to December 2010, as part of the California State Water Resources Control Board (SWRCB) Groundwater Ambient Monitoring and Assessment (GAMA) Program’s Priority Basin Project (PBP). The GAMA-PBP was developed in response to the California Groundwater Quality Monitoring Act of 2001 and is being conducted in collaboration with the SWRCB and Lawrence Livermore National Laboratory (LLNL). The KLAM study unit was the thirty-third study unit to be sampled as part of the GAMA-PBP. The GAMA Klamath Mountains study was designed to provide a spatially unbiased assessment of untreated-groundwater quality in the primary aquifer system and to facilitate statistically consistent comparisons of untreated-groundwater quality throughout California. The primary aquifer system is defined by the perforation intervals of wells listed in the California Department of Public Health (CDPH) database for the KLAM study unit. Groundwater quality in the primary aquifer system may differ from the quality in the shallower or deeper water-bearing zones; shallower groundwater may be more vulnerable to surficial contamination. In the KLAM study unit, groundwater samples were collected from sites in Del Norte, Siskiyou, Humboldt, Trinity, Tehama, and Shasta Counties, California. Of the 39 sites sampled, 38 were selected by using a spatially distributed, randomized grid-based method to provide statistical representation of the primary aquifer system in the study unit (grid sites), and the remaining site was non-randomized (understanding site). The groundwater samples were analyzed for basic field parameters, organic constituents (volatile organic compounds [VOCs] and pesticides and pesticide degradates), inorganic constituents (trace elements, nutrients, major and minor ions, total dissolved solids [TDS]), radon-222, gross alpha and gross beta

Impacts of swine manure pits on groundwater quality

International Nuclear Information System (INIS)

Krapac, I.G.; Dey, W.S.; Roy, W.R.; Smyth, C.A.; Storment, E.; Sargent, S.L.; Steele, J.D.

2002-01-01

New information is presented on impacts on groundwater by manure storage in deep ground pits. - Manure deep-pits are commonly used to store manure at confined animal feeding operations. However, previous to this study little information had been collected on the impacts of deep-pits on groundwater quality to provide science-based guidance in formulating regulations and waste management strategies that address risks to human health and the environment. Groundwater quality has been monitored since January 1999 at two hog finishing facilities in Illinois that use deep-pit systems for manure storage. Groundwater samples were collected on a monthly basis and analyzed for inorganic and bacteriological constituent concentrations. The two sites are located in areas with geologic environments representing different vulnerabilities for local groundwater contamination. One site is underlain by more than 6 m of clayey silt, and 7-36 m of shale. Concentrations of chloride, ammonium, phosphate, and potassium indicated that local groundwater quality had not been significantly impacted by pit leakage from this facility. Nitrate concentrations were elevated near the pit, often exceeding the 10 mg N/l drinking water standard. Isotopic nitrate signatures suggested that the nitrate was likely derived from soil organic matter and fertilizer applied to adjacent crop fields. At the other site, sandstone is located 4.6-6.1 m below land surface. Chloride concentrations and δ 15 N and δ 18 O values of dissolved nitrate indicated that this facility may have limited and localized impacts on groundwater. Other constituents, including ammonia, potassium, phosphate, and sodium were generally at or less than background concentrations. Trace- and heavy-metal concentrations in groundwater samples collected from both facilities were at concentrations less than drinking water standards. The concentration of inorganic constituents in the groundwater would not likely impact human health. Fecal

Impacts of swine manure pits on groundwater quality

Energy Technology Data Exchange (ETDEWEB)

Krapac, I.G.; Dey, W.S.; Roy, W.R.; Smyth, C.A.; Storment, E.; Sargent, S.L.; Steele, J.D

2002-12-01

New information is presented on impacts on groundwater by manure storage in deep ground pits. - Manure deep-pits are commonly used to store manure at confined animal feeding operations. However, previous to this study little information had been collected on the impacts of deep-pits on groundwater quality to provide science-based guidance in formulating regulations and waste management strategies that address risks to human health and the environment. Groundwater quality has been monitored since January 1999 at two hog finishing facilities in Illinois that use deep-pit systems for manure storage. Groundwater samples were collected on a monthly basis and analyzed for inorganic and bacteriological constituent concentrations. The two sites are located in areas with geologic environments representing different vulnerabilities for local groundwater contamination. One site is underlain by more than 6 m of clayey silt, and 7-36 m of shale. Concentrations of chloride, ammonium, phosphate, and potassium indicated that local groundwater quality had not been significantly impacted by pit leakage from this facility. Nitrate concentrations were elevated near the pit, often exceeding the 10 mg N/l drinking water standard. Isotopic nitrate signatures suggested that the nitrate was likely derived from soil organic matter and fertilizer applied to adjacent crop fields. At the other site, sandstone is located 4.6-6.1 m below land surface. Chloride concentrations and {delta}{sup 15}N and {delta}{sup 18}O values of dissolved nitrate indicated that this facility may have limited and localized impacts on groundwater. Other constituents, including ammonia, potassium, phosphate, and sodium were generally at or less than background concentrations. Trace- and heavy-metal concentrations in groundwater samples collected from both facilities were at concentrations less than drinking water standards. The concentration of inorganic constituents in the groundwater would not likely impact human

Phosphate interference during in situ treatment for arsenic in groundwater.

Science.gov (United States)

Brunsting, Joseph H; McBean, Edward A

2014-01-01

Contamination of groundwater by arsenic is a problem in many areas of the world, particularly in West Bengal (India) and Bangladesh, where reducing conditions in groundwater are the cause. In situ treatment is a novel approach wherein, by introduction of dissolved oxygen (DO), advantages over other treatment methods can be achieved through simplicity, not using chemicals, and not requiring disposal of arsenic-rich wastes. A lab-scale test of in situ treatment by air sparging, using a solution with approximately 5.3 mg L(-1) ferrous iron and 200 μg L(-1) arsenate, showed removal of arsenate in the range of 59%. A significant obstacle exists, however, due to the interference of phosphate since phosphate competes for adsorption sites on oxidized iron precipitates. A lab-scale test including 0.5 mg L(-1) phosphate showed negligible removal of arsenate. In situ treatment by air sparging demonstrates considerable promise for removal of arsenic from groundwater where iron is present in considerable quantities and phosphates are low.

Isotope variations of dissolved Zn in the Rio Grande watershed, USA: The role of adsorption on Zn isotope composition

Science.gov (United States)

Szynkiewicz, Anna; Borrok, David M.

2016-01-01

In order to better understand the factors influencing zinc (Zn) isotope composition in hydrological systems, we analyzed the δ66Zn of dissolved Zn in the streams and groundwater of the Upper and Middle Rio Grande watershed in Colorado and New Mexico, United States. The stream water samples have a wider variation of δ66Zn (-0.57 to + 0.41 ‰ relative to the JMC 3-0749-Lyon standard) than groundwater samples (-0.13 to + 0.12 ‰) and than samples from streams that are in close proximity to abandoned mining sites (+0.24 to + 0.40 ‰). Regional changes of bedrock geology, from primarily igneous rocks to primarily sedimentary rocks, have no resolvable effect on the δ66Zn of aqueous samples. Instead, an increase in water pH from 7.5 to 8.5 corresponds to a considerable decrease in the δ66Zn of dissolved Zn (R2 = - 0.37, p = 0.003, n = 22). Consequently, we link the observed Zn isotope variations to the process of adsorption of Zn onto suspended sediment and bedrock minerals (average Δ66Znadsorbed-dissolved = + 0.31 ‰). Our results are in good agreement with previous experimental and empirical studies suggesting that Zn adsorption leads to a residual dissolved pool enriched in light Zn isotopes. Given that anthropogenic Zn sources can also be responsible for lowering of δ66Zn, and may overlap with the pH/adsorption effect on δ66Zn, the latter needs to be carefully considered in future studies to differentiate between natural and anthropogenic factors influencing Zn isotopes in this and other aquatic systems.

Municipal waste management and groundwater contamination processes in Córdoba Province, Argentina

Directory of Open Access Journals (Sweden)

Daniel Emilio Martínez

2010-12-01

Full Text Available In Coronel Moldes, Argentina, waste management practices consist in municipal waste being tipped directly onto an area of sand dunes at the municipal waste disposal site (MWDS. Moreover, untreated liquid waste from septic tanks and latrines from urban areas are discharged in the same place. This co-disposal waste management is very common in many regions of Argentina and its impact on the groundwater of Coronel Moldes has not been evaluated. The study area is located in the vicinity of a MWDS in a flatlands environment that is typical of Argentina. The main objective of this study was to evaluate the impacts on groundwater quality of current waste management practices in order to consider the requirement for new guidelines for sustainable groundwater management. Three groundwater monitoring wells were installed up-, across- and down-gradient of the MWDS. The principal aquifer is formed by sandy silt sediments (loess. Groundwater levels in the area of the MWDS are between 5.6 m and 7.8 m. The Vulnerability index indicates that groundwater in this area has a high vulnerability. Groundwater in the vicinity of the MWDS shows elevated electrical conductivity, high concentrations of Cl-, Na+, and HCO3- ions, COD, BOD5 and aerobic bacteria and less dissolved oxygen than the background values indicating the presence of organic matter. Municipal waste management represents a significant omission in current groundwater protection policy at Coronel Moldes. Strict supervision of solid and liquid municipal waste disposal needs to be instigated in order to ensure that the groundwater remains free of contamination and to allow a sustainable environmental management.

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.

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.

The Slow Moving Threat of Groundwater Salinization: Mechanisms, Costs, and Adaptation Strategies

Science.gov (United States)

Pauloo, R.; Guo, Z.; Fogg, G. E.

2016-12-01

Population growth, the Green Revolution, and climate uncertainties have accelerated overdraft in groundwater basins worldwide, which in some regions is converting these basins into closed hydrologic systems, where the dominant exits for water are evapotranspiration and pumping. Irrigated agricultural basins are particularly at risk to groundwater salinization, as naturally occurring (i.e., sodium, potassium, chloride) and anthropogenic (i.e., nitrate fertilizers) salts leach back into the water table through the root zone, while a large portion of pumped groundwater leaves the system as it is evapotranspired by crops. Decreasing water quality associated with increases in Total Dissolved Solids (TDS) has been documented in aquifers across the United States in the past half century. This study suggests that the increase in TDS in aquifers can be partially explained by closed basin hydrogeology and rock-water interactions leading to groundwater salinization. This study will present: (1) a report on historical water quality in the Tulare basin, (2) a forward simulation of salt balance in Tulare Basin based on the Department of Water Resources numerical model C2VSim, and a simple mixing model, (3) an economic analysis forecasting the cost of desalination under varying degrees of managed groundwater recharge where the basin is gradually filled, avoiding hydraulic closure.

Fast Oxidation Processes in a Naturally Reduced Aquifer Zone Caused by Dissolved Oxygen

Science.gov (United States)

Davis, J. A.; Jemison, N. E.; Williams, K. H.; Hobson, C.; Bush, R. P.

2014-12-01

The occurrence of naturally reduced zones is quite common in alluvial aquifers in the western U.S.A. due to the burial of woody debris in flood plains. The naturally reduced zones are heterogeneously dispersed in such aquifers and are characterized by high concentrations of organic carbon and reduced phases, including iron sulfides and reduced forms of metals, including uranium(IV). The persistence of high concentrations of dissolved uranium(VI) at uranium-contaminated aquifers on the Colorado Plateau has been attributed to slow oxidation of insoluble uranium(IV) mineral phases that are found in association with these natural reducing zones, although there is little understanding of the relative importance of various potential oxidants. Three field experiments were conducted within an alluvial aquifer adjacent to the Colorado River near Rifle, CO wherein groundwater associated with naturally reduced zones was pumped into a gas-impermeable tank, mixed with a conservative tracer (Br-), bubbled with a gas phase composed of 97% O2 and 3% CO2, and then returned to the subsurface in the same well from which it was withdrawn. Within minutes of re-injection of the oxygenated groundwater, dissolved uranium(VI) concentrations increased from less than 1 μM to greater than 2.5 μM, demonstrating that oxygen can be an important oxidant for uranium in these field systems if supplied to the naturally reduced zones. Small concentrations of nitrate were also observed in the previously nitrate-free groundwater, and Fe(II) decreased to the detection limit. These results contrast with other laboratory and field results in which oxygen was introduced to systems containing high concentrations of mackinawite (FeS) rather than the more crystalline iron sulfides found in aged, naturally reduced zones. The flux of oxygen to the naturally reduced zones in the alluvial aquifers occurs mainly through interactions between groundwater and gas phases at the water table, and seasonal variations

Effluents from a waste rock deposit of a former uranium mine in Saxony/Germany - Mass flow balance of water and dissolved solids

International Nuclear Information System (INIS)

Biehler, D.

2002-01-01

Soon after uranium mining had ceased in eastern Germany in 1990, work for remediation of several mining sites began. The Wismut GmbH, owner of the Mine of Dresden-Gittersee's waste rock dump, introduced the concept of reducing the impact to the environment via water and air paths by implementing a multi-layer soil cover. The deposit consists mainly of waste rock (clastic sediments of Doehlener Becken, deep metamorphic rocks) but also of low-grade ore (U-rich coal) and tailing materials. At the time when remediation started, the effluents completely infiltrated the underground. Because of previous surface exfiltration activities, they were already known to be very rich in dissolved solids, especially in sulphate and uranium. As demanded by the state authorities, the owner funded a vast hydrogeological study of the site. In testing the efficiency of surface sealing, the study indicated a mass flow balance of water and dissolved solids for the current situation, and predicted emissions into the water path which would occur after realisation of the proposed soil cover. The field investigation program consisted of: measurements of flow, of concentrations of dissolved solids (esp. U and Ra-226) and of contents of environmental isotopes in precipitation, surface runoff, seepage water and groundwater in the current condition of the dump; the study of waste rock material (geochemistry, mineralogy); waste rock material elution tests; underground investigation by drilling boreholes up to 270 m in depth. The resulting data allowed for: a hydrogeological conceptual model of the site; a consistent mass flow balance for the current condition of the dump; a prediction of concentrations in groundwater resulting after the realisation of a soil cover. The predictions show that the concentrations of dissolved solids in the contaminated groundwater would be significantly decreased. Furthermore it would be possible to reach the standards for drinking water with respect to uranium

Groundwater-quality data in the Bear Valley and Selected Hard Rock Areas study unit, 2010: Results from the California GAMA Program

Science.gov (United States)

Mathany, Timothy M.; Belitz, Kenneth

2013-01-01

pesticide degradates, pharmaceutical compounds, and wastewater indicator compounds [WICs]), constituents of special interest (perchlorate, N-nitrosodimethylamine [NDMA], and 1,2,3-trichloropropane [1,2,3-TCP]), and inorganic constituents (trace elements, nutrients, dissolved organic carbon [DOC], major and minor ions, silica, total dissolved solids [TDS], alkalinity, and arsenic and iron species), and uranium and other radioactive constituents (radon-222 and activities of tritium and carbon-14). Isotopic tracers (of hydrogen and oxygen in water, of nitrogen and oxygen in dissolved nitrate, of dissolved boron, isotopic ratios of strontium in water, and of carbon in dissolved inorganic carbon) and dissolved noble gases (argon, helium-4, krypton, neon, and xenon) were measured to help identify the sources and ages of sampled groundwater. In total, groundwater samples were analyzed for 289 unique constituents and 8 water-quality indicators in the BEAR study unit. Quality-control samples (blanks, replicate pairs, or matrix spikes) were collected at 13 percent of the sites in the BEAR study unit, and the results for these samples were used to evaluate the quality of the data from the groundwater samples. Blank samples rarely contained detectable concentrations of any constituent, indicating that contamination from sample collection or analysis was not a significant source of bias in the data for the groundwater samples. Replicate pair samples all were within acceptable limits of variability. Matrix-spike sample recoveries were within the acceptable range (70 to 130 percent) for approximately 84 percent of the compounds. This study did not evaluate the quality of water delivered to consumers. After withdrawal, groundwater typically is treated, disinfected, and (or) blended with other waters to maintain water quality. Regulatory benchmarks apply to water that is delivered to the consumer, not to untreated groundwater. However, to provide some context for the results, concentrations

Physicochemical Assessment of Surface and Groundwater Quality of the Greater Chittagong Region of Bangladesh

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M. J. Ahmed

2010-12-01

Full Text Available The study was carried out to assess surface and groundwater quality of the greater Chittagong (Chittagong and Cox’s Bazar districts and Chittagong Hill Tracts (Rangamati, Khagrachhari and Bandarban districts of Bangladesh. To study the various physicochemical and microbiological parameters, surface water samples from the Karnafuli, Halda, Sangu, Matamuhuri, Bakkhali, Naf, Kasalong, Chingri and Mayani Rivers, Kaptai Lake and groundwater samples from almost every Upazilas, smaller administrative unit of Bangladesh, were collected and analyzed. The statistical methods of sampling were used for collecting samples. Samples were preserved using suitable preservation methods. Water samples from the freshwater resources were collected from different points and tide conditions and at different seasons for continuous monitoring during the hydrological years 2008-2009. The collected samples were analyzed for the following parameters: pH, electrical conductivity (EC, total dissolved solids (TDS, total suspended solids (TSS, total solids (TS, dissolved oxygen (DO, transparency, acidity, dissolved carbon dioxide, total alkalinity, total hardness, chloride, ammonia-N, hydrogen sulfide, sulphate-S, o-phosphate-P, biochemical oxygen demand (BOD, chemical oxygen demand (COD, nitrate-N, nitrite-N, total nitrite and nitrate-N, arsenic, iron, manganese, copper, nickel, chromium, cadmium, lead, calcium, magnesium, sodium and potassium using the procedure outlined in the standard methods. Average values of maximum physicochemical and microbiological parameters studied for the Karnafuli River were found higher than the World Health Organization (WHO guideline. The maximum water quality parameters of Kaptai Lake and other Rivers of Chittagong region were existed within the permissible limits of WHO guideline. The data showed the water quality slightly differs in pre-monsoon and post-monsoon than monsoon season. The concentration of different constituents of most of

Chemical Evolution of Groundwater Near a Sinkhole Lake, Northern Florida: 2. Chemical Patterns, Mass Transfer Modeling, and Rates of Mass Transfer Reactions

Science.gov (United States)

Katz, Brian G.; Plummer, L. Niel; Busenberg, Eurybiades; Revesz, Kinga M.; Jones, Blair F.; Lee, Terrie M.

1995-06-01

Chemical patterns along evolutionary groundwater flow paths in silicate and carbonate aquifers were interpreted using solute tracers, carbon and sulfur isotopes, and mass balance reaction modeling for a complex hydrologic system involving groundwater inflow to and outflow from a sinkhole lake in northern Florida. Rates of dominant reactions along defined flow paths were estimated from modeled mass transfer and ages obtained from CFC-modeled recharge dates. Groundwater upgradient from Lake Barco remains oxic as it moves downward, reacting with silicate minerals in a system open to carbon dioxide (CO2), producing only small increases in dissolved species. Beneath and downgradient of Lake Barco the oxic groundwater mixes with lake water leakage in a highly reducing, silicate-carbonate mineral environment. A mixing model, developed for anoxic groundwater downgradient from the lake, accounted for the observed chemical and isotopic composition by combining different proportions of lake water leakage and infiltrating meteoric water. The evolution of major ion chemistry and the 13C isotopic composition of dissolved carbon species in groundwater downgradient from the lake can be explained by the aerobic oxidation of organic matter in the lake, anaerobic microbial oxidation of organic carbon, and incongruent dissolution of smectite minerals to kaolinite. The dominant process for the generation of methane was by the CO2 reduction pathway based on the isotopic composition of hydrogen (δ2H(CH4) = -186 to -234‰) and carbon (δ13C(CH4) = -65.7 to -72.3‰). Rates of microbial metabolism of organic matter, estimated from the mass transfer reaction models, ranged from 0.0047 to 0.039 mmol L-1 yr-1 for groundwater downgradient from the lake.

Assessing quality and quantity of groundwater DOC in relation to plant export from different over-winter green-cover treatments in tillage farming systems

Science.gov (United States)

Premrov, Alina; Coxon, Catherine; Hackett, Richard; Richards, Karl

2010-05-01

The biogeochemistry of nitrogen is often connected to carbon and C/N dynamics. The dissolved organic carbon (DOC) electron donor availability can be related to groundwater denitrification (Buss, et al. 2005). Therefore groundwater nitrate attenuation processes are also frequently linked to carbon availability. In recent years the role of over-winter green cover in tillage farming has been studied extensively. Nevertheless further research on the biogeochemical effect of green cover on soil/sediment and groundwater quality is still needed. In particular plant roots are known to exude different types of organic compounds, but their role in groundwater quality has not been investigated in depth. According to Cannavo et al. (2004a,b), in addition to quantity, the quality of water-extractable soil organic matter (e.g. molecular size/weight) has also an important role for microbial activity. In this study we investigate the effect of over-winter green-cover on potential DOC export to shallow groundwater (2 - 5 m below ground level), located on tillage land in Oak Park, Carlow, Ireland. The experiment includes three over-winter green-cover treatments: natural green-cover, mustard and no-cover (sprayed with herbicide following harvest); and is underlain by a sand and gravel aquifer. The site is equipped with 4 shallow piezometers per treatment (total no. of piezometers is 20, including treatments and surrounding piezometers). In addition to monitoring the quantity of DOC concentrations in shallow groundwater under different green cover treatments over time, an attempt was made to evaluate the quality of dissolved organic matter in shallow groundwater using Excitation Emission Fluorescence Matrix (EEFM) profiles obtained from analyses performed on a Varian Fluorescence Spectrophotometer of a single batch of samples (from all 20 installed piezometers in September 2009). To evaluate the quality of dissolved organic matter in shallow groundwater, computation of the

Surface-water and groundwater interactions in an extensively mined watershed, upper Schuylkill River, Pennsylvania, USA

Science.gov (United States)

Cravotta,, Charles A.; Goode, Daniel J.; Bartles, Michael D.; Risser, Dennis W.; Galeone, Daniel G.

2014-01-01

Streams crossing underground coal mines may lose flow, while abandoned mine drainage (AMD) restores flow downstream. During 2005-12, discharge from the Pine Knot Mine Tunnel, the largest AMD source in the upper Schuylkill River Basin, had near-neutral pH and elevated concentrations of iron, manganese, and sulfate. Discharge from the tunnel responded rapidly to recharge but exhibited a prolonged recession compared to nearby streams, consistent with rapid infiltration and slow release of groundwater from the mine. Downstream of the AMD, dissolved iron was attenuated by oxidation and precipitation while dissolved CO2 degassed and pH increased. During high-flow conditions, the AMD and downstream waters exhibited decreased pH, iron, and sulfate with increased acidity that were modeled by mixing net-alkaline AMD with recharge or runoff having low ionic strength and low pH. Attenuation of dissolved iron within the river was least effective during high-flow conditions because of decreased transport time coupled with inhibitory effects of low pH on oxidation kinetics. A numerical model of groundwater flow was calibrated using groundwater levels in the Pine Knot Mine and discharge data for the Pine Knot Mine Tunnel and the West Branch Schuylkill River during a snowmelt event in January 2012. Although the calibrated model indicated substantial recharge to the mine complex took place away from streams, simulation of rapid changes in mine pool level and tunnel discharge during a high flow event in May 2012 required a source of direct recharge to the Pine Knot Mine. Such recharge produced small changes in mine pool level and rapid changes in tunnel flow rate because of extensive unsaturated storage capacity and high transmissivity within the mine complex. Thus, elimination of stream leakage could have a small effect on the annual discharge from the tunnel, but a large effect on peak discharge and associated water quality in streams.

Hydraulic performance of permeable barriers for in situ treatment of contaminated groundwater

International Nuclear Information System (INIS)

Smyth, D.J.A.; Shikaze, S.G.; Cherry, J.A.

1997-01-01

The passive interception and in situ treatment of dissolved contaminants in groundwater by permeable reactive barriers has recently gained favor at an increasing number of sites as an alternative to conventional approaches to groundwater remediation such as the pump-and-treat method. Permeable reactive barriers have two essential functions. The first is that the barriers must be installed in a position such that all of the plume passes through the reactive system. The second function is to achieve acceptable treatment of the contamination by physical, chemical or biological means within or downgradient of the barrier. In this paper, issues associated with the hydraulic performance of permeable reaction barriers are evaluated using a three-dimensional groundwater flow model. The efficiency of plume capture by permeable wall and funnel-and-gate systems is examined for some generic and for site-specific hydrogeologic systems. The results have important implications to decisions pertaining to the selection, design and installation of permeable reactive barrier systems

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.

Restoration of groundwater after solution mining at the Highland Uranium Project, Wyoming, USA

Energy Technology Data Exchange (ETDEWEB)

Hunter, J. [Waste Technology Group, British Nuclear Fuels PLC, Risley, Warrington (United Kingdom); Huffman, L. [Power Resources Inc., Highland Uranium Mine, Glenrock, Wyoming (United States)

2000-07-01

The Highland Project, located in Converse County, Wyoming, has had a successful 11 year history of in-situ leach mining of Tertiary roll-front uranium deposits. The uranium ore is oxidized and solubilized by circulating native groundwater, containing additional dissolved O{sub 2} and CO{sub 2}, within confined fluvial aquifers at depths of 200 - 250 m. The changing chemistry of this groundwater during leaching is discussed, as are the various treatment techniques that have been used to restore this fluid at the end of mining. Examples are provided which demonstrate the varying effectiveness of each technique for the reduction of elevated concentrations of different groundwater parameters. The complications arising from the proximity of the earliest wellfields to abandoned, conventional mine workings, as well as unexpected side effects from each restoration method, have combined to make an interesting case history from this long established mining operation. (author)

Excess air in groundwater as a potential indicator of past environmental changes

International Nuclear Information System (INIS)

Aeschenbach-Hertig, W.; Beyerle, U.; Holocher, J.; Peeters, F.; Kipfer, R.

2002-01-01

Dissolved noble gases in groundwater are used to reconstruct paleotemperature, but also yield information about 'excess air', a component of dissolved gases in excess of solubility equilibrium, derived from dissolution of trapped air in the ground. A good characterization of the excess air component is necessary not only to obtain reliable noble gas temperatures, but also to investigate the potential of excess air as a proxy for past environmental conditions. Two excess air related quantities can be derived from groundwater noble gas data sets: The initial air/water ratio and the pressure exerted on the entrapped air. Under recharge conditions typical for many aquifers, the excess of dissolved gases, expressed by the relative Ne excess ΔNe, is mainly determined by the hydrostatic pressure on the entrapped air. Thus, we suggest that ΔNe is essentially a measure of the amplitude of water table fluctuations in the recharge area. Comparing data sets from three aquifers in temperate, humid latitudes and three aquifers in tropical, semi-arid regions, we find that ΔNe is generally higher in the tropical aquifers, possibly related to larger water table fluctuations in these aquifers characterized by deep unsaturated zones. Whereas ΔNe shows little temporal variation in the mid-latitude aquifers, there is a strong signal of higher ΔNe in the paleowaters of the tropical aquifers as compared to water recharged under modern climate conditions. This finding may indicate a higher variability of recharge in the past at the studied tropical sites. (author)

Quality assessment of surface and groundwater of Taluka Daur, district Nawabshah, Sindh, Pakistan

International Nuclear Information System (INIS)

Majidano, S.A.; Khuhawar, M.Y.; Channar, A.H.

2010-01-01

In present work groundwater and surface water samples are analyzed from Taluka Daur, district Nawabshah, Sindh. 38 water samples of the study area were examined. The physico-chemical parameters of the water samples were found in the following ranges pH 6.64-8.18, total dissolved salts (TDS) 188-26752 mg/L, HCO/sub 3/ 27-5011 mg/L, total hardness (TH) 62-13200 mg/L, chloride 41-13953 mg/L, SO/sub 4/ 23-5122 mg/L, ortho-phosphate (P) 0.09-0.144 mg/L, total phosphate (P) 0.097-0.925 mg/L, NO/sub 2/-N 0-0.662 mg/L, NO/sub 3/-N 0.02-1.993 mg/L and dissolved oxygen 1.1-10.0 mg/L. The concentration of essential metal ions (Na, Ca, Mg, and K) was found in the ranges of 18-4600 mg/L, 12-3610 mg/L, 4-1308 mg/L and 3-570 mg/L, respectively. Only ten samples were found suitable and rest of the samples were unsuitable for human consumption. The study shows that the groundwater of the major portion of study area is not suitable for drinking purpose. (author)

Chemical and isotopic compositions of water and dissolved sulfate from shallow wells on Vulcano Island, Aeolian Archipelago, Italy

Energy Technology Data Exchange (ETDEWEB)

Cortecci, G.; Dinelli, E.; Boschetti, T. [University of Bologna (Italy). Dept. of Earth and Geological Environmental Sciences; Bolognesi, L. [International Institute for Geothermal Research, Pisa (Italy); Ferrara, G. [University of Pisa (Italy). Dept. of Earth Sciences

2001-02-01

Twenty-two cold and thermal waters from shallow wells sampled in June 1995 in the Vulcano Porto area, Vulcano Island, were analyzed for major and minor chemical constituents, oxygen and hydrogen isotopes and tritium contents, and sulfur isotopes in the dissolved sulfate. The sulfur isotopic composition of the dissolved sulfate ranges between + 0.6 and + 6.5 per mille (mean + 3.7{+-}1.7 per mille), and is interpreted as deriving mainly from fumarolic SO{sub 2} undergoing oxidation in deep and shallow aquifers, with possible minor contributions from oxidation of H{sub 2}S. Dissolution of secondary anhydrite may have been a minor source of the isotopically heavy aqueous sulfate in the cold groundwaters. The chemical and isotopic features of the waters support previous interpretative hydrologic models of Vulcano Porto, which comprise a number of aquifers fed basically by two major end-members, i.e. meteoric water and crater-type fumarolic inputs, the latter in the form of absorbed emissions or condensate. These data, along with the sulfur isotopes of aqueous sulfate, exclude involvement of seawater in the recharge of the groundwater system of the island. (author)

Effects of groundwater withdrawals from the Hurricane Fault zone on discharge of saline water from Pah Tempe Springs, Washington County, Utah

Science.gov (United States)

Gardner, Philip M.

2018-04-10

Pah Tempe Springs, located in Washington County, Utah, contribute about 95,000 tons of dissolved solids annually along a 1,500-foot gaining reach of the Virgin River. The river gains more than 10 cubic feet per second along the reach as thermal, saline springwater discharges from dozens of orifices located along the riverbed and above the river on both banks. The spring complex discharges from fractured Permian Toroweap Limestone where the river crosses the north-south trending Hurricane Fault. The Bureau of Reclamation Colorado River Basin Salinity Control Program is evaluating the feasibility of capturing and desalinizing the discharge of Pah Tempe Springs to improve downstream water quality in the Virgin River. The most viable plan, identified by the Bureau of Reclamation in early studies, is to capture spring discharge by pumping thermal groundwater from within the Hurricane Fault footwall damage zone and to treat this water prior to returning it to the river.Three multiple-day interference tests were conducted between November 2013 and November 2014, wherein thermal groundwater was pumped from fractured carbonate rock in the fault damage zone at rates of up to 7 cubic feet per second. Pumping periods for these tests lasted approximately 66, 74, and 67 hours, respectively, and the tests occurred with controlled streamflows of approximately 2.0, 3.5, and 24.5 cubic feet per second, respectively, in the Virgin River upstream from the springs reach. Specific conductance, water temperature, and discharge were monitored continuously in the river (upstream and downstream of the springs reach) at selected individual springs, and in the pumping discharge during each of the tests. Water levels were monitored in three observation wells screened in the thermal system. Periodic stream and groundwater samples were analyzed for dissolved-solids concentration and the stable isotopes of oxygen and hydrogen. Additional discrete measurements of field parameters (specific

Effects of clay minerals, hydroxides, and timing of dissolved organic matter addition on the competitive sorption of copper, nickel, and zinc : a column experiment

NARCIS (Netherlands)

Refaey, Y.; Jansen, B.; Parsons, J.R.; de Voogt, P.; Bagnis, S.; Markus, A.; El-Shater, A.-H.; El-Haddad, A.-A.; Kalbitz, K.

2017-01-01

Infiltration of heavy metal (HM) polluted wastewater can seriously compromise soil and groundwater quality. Interactions between mineral soil components (e.g. clay minerals) and dissolved organic matter (DOM) play a crucial role in determining HM mobility in soils. In this study, the influence of

Quasi-three-dimensional analysis of ground water flow and dissolved multicomponent solute transport in saturated porous media

International Nuclear Information System (INIS)

Tang, Yi.

1991-01-01

A computational procedure was developed in this study to provide flexibility needed in the application of three-dimensional groundwater flow and dissolved multicomponent solute transport simulations. In the first part of this study, analytical solutions were proposed for the dissolved single-component solute transport problem. These closed form solutions were developed for homogeneous but stratified porous media. This analytical model took into account two-dimensional diffusion-advection in the main aquifer layer and one-dimensional diffusion-advection in the adjacent aquitards, as well as first order radioactive decay and linear adsorption isotherm in both aquifer and aquitards. The associated analytical solutions for solute concentration distributions in the aquifer and aquitards were obtained using Laplace Transformation and Method of Separation of Variables techniques. Next, in order to analyze the problem numerically, a quasi-three-dimensional finite element algorithm was developed based on the multilayer aquifer concept. In this phase, advection, dispersion, adsorption and first order multi-species chemical reaction terms were included to the analysis. Employing this model, without restriction on groundwater flow pattern in the multilayer aquifer system, one may analyze the complex behavior of the groundwater flow and solute movement pattern in the system. These numerical models may be utilized as calibration tools in site characterization studies, or as predictive models during the initial stages of a typical site investigation study. Through application to several test and field problems, the usefulness, accuracy and efficiency of the proposed models were demonstrated. Comparison of results with analytical solution, experimental data and other numerical methods were also discussed

Nitrate pollution of groundwater; all right…, but nothing else?

Energy Technology Data Exchange (ETDEWEB)

Menció, Anna, E-mail: anna.mencio@udg.edu [Grup de Geologia Aplicada i Ambiental (GAiA), Centre de Recerca en Geologia i Cartografia Ambiental (Geocamb), Deptartament de Ciències Ambientals, Facultat de Ciències, Universitat de Girona, 17071 Girona (Spain); Mas-Pla, Josep, E-mail: jmas@icra.cat [Grup de Geologia Aplicada i Ambiental (GAiA), Centre de Recerca en Geologia i Cartografia Ambiental (Geocamb), Deptartament de Ciències Ambientals, Facultat de Ciències, Universitat de Girona, 17071 Girona (Spain); Institut Català de Recerca de l’Aigua (ICRA) (Spain); Otero, Neus, E-mail: notero@ub.edu [Grup de Mineralogia Aplicada i Geoquímica de Fluids, Departament de Cristallografia, Mineralogia i Dipòsits Minerals, Facultat de Geologia, Universitat de Barcelona (UB), C/ Martí i Franquès, s/n – 08028 Barcelona (Spain); Regàs, Oriol [Grup de Geologia Aplicada i Ambiental (GAiA), Centre de Recerca en Geologia i Cartografia Ambiental (Geocamb), Deptartament de Ciències Ambientals, Facultat de Ciències, Universitat de Girona, 17071 Girona (Spain); Boy-Roura, Mercè [Institut Català de Recerca de l’Aigua (ICRA) (Spain); and others

2016-01-01

Contamination from agricultural sources and, in particular, nitrate pollution, is one of the main concerns in groundwater management. However, this type of pollution entails the entrance of other substances into the aquifer, as well as it may promote other processes. In this study, we deal with hydrochemical and isotopic analysis of groundwater samples from four distinct zones in Catalonia (NE Spain), which include 5 different aquifer types, to investigate the influence of fertilization on the overall hydrochemical composition of groundwater. Results indicate that intense fertilizer application, causing high nitrate pollution in aquifers, also homogenize the contents of the major dissolved ions (i.e.; Cl{sup -}, SO{sub 4}{sup 2-}, Ca{sup 2+}, Na{sup +}, K{sup +}, and Mg{sup 2+}). Thus, when groundwater in igneous and sedimentary aquifers is compared, significant differences are observed under natural conditions for Cl{sup -}, Na{sup +} and Ca{sup 2+} (with p-values ranging from < 0.001 to 0.038), and when high nitrate concentrations occur, these differences are reduced (most p-values ranged between 0.054 and 0.978). Moreover, positive linear relationships between nitrate and some ions are found indicating the magnitude of the fertilization impact on groundwater hydrochemistry (with R{sup 2} values of 0.490, 0.609 and 0.470, for SO{sub 4}{sup 2-}, Ca{sup 2+} and Cl{sup -}, respectively). Nevertheless, the increasing concentration of specific ions is not only attributed to agricultural pollution, but to their enhancing effect upon the biogeochemical processes that control water-rock interactions. Such results raise awareness that these processes should be evaluated in advance in order to assess an adequate groundwater resources management. - Highlights: • The effects of nitrate pollution have been evaluated in five different aquifer types • Statistical and multivariate analyses are used to identify groundwater changes • Agricultural pollution modifies

Contributions of Phosphorus from Groundwater to Streams in the Piedmont, Blue Ridge, and Valley and Ridge Physiographic Provinces, Eastern United States

Science.gov (United States)

Denver, Judith M.; Cravotta,, Charles A.; Ator, Scott W.; Lindsey, Bruce D.

2011-01-01

Phosphorus from natural and human sources is likely to be discharged from groundwater to streams in certain geochemical environments. Water-quality data collected from 1991 through 2007 in paired networks of groundwater and streams in different hydrogeologic and land-use settings of the Piedmont, Blue Ridge, and Valley and Ridge Physiographic Provinces in the eastern United States were compiled and analyzed to evaluate the sources, fate, and transport of phosphorus. The median concentrations of phosphate in groundwater from the crystalline and siliciclastic bedrock settings (0.017 and 0.020 milligrams per liter, respectively) generally were greater than the median for the carbonate setting (less than 0.01 milligrams per liter). In contrast, the median concentrations of dissolved phosphate in stream base flow from the crystalline and siliciclastic bedrock settings (0.010 and 0.014 milligrams per liter, respectively) were less than the median concentration for base-flow samples from the carbonate setting (0.020 milligrams per liter). Concentrations of phosphorus in many of the stream base-flow and groundwater samples exceeded ecological criteria for streams in the region. Mineral dissolution was identified as the dominant source of phosphorus in the groundwater and stream base flow draining crystalline or siliciclastic bedrock in the study area. Low concentrations of dissolved phosphorus in groundwater from carbonate bedrock result from the precipitation of minerals and (or) from sorption to mineral surfaces along groundwater flow paths. Phosphorus concentrations are commonly elevated in stream base flow in areas underlain by carbonate bedrock, however, presumably derived from in-stream sources or from upland anthropogenic sources and transported along short, shallow groundwater flow paths. Dissolved phosphate concentrations in groundwater were correlated positively with concentrations of silica and sodium, and negatively with alkalinity and concentrations of calcium

Hydrogeologic framework, arsenic distribution, and groundwater geochemistry of the glacial-sediment aquifer at the Auburn Road landfill superfund site, Londonderry, New Hampshire

Science.gov (United States)

Degnan, James R.; Harte, Philip T.

2013-01-01

been observed in the wetland, streams, and pond downgradient of the landfills. Piezometers were installed in some of these locations to confirm groundwater discharge, measure vertical-flow gradients, and to provide a way to sample the discharging groundwater. Understanding the movement of leachate in groundwater is complicated by the presence of preferential flow paths through aquifer materials with differing hydraulic properties; these preferential flow paths can affect rates of recharge, geochemical conditions, and contaminant fluxes. In areas adjacent to the three capped landfills, infiltration of precipitation containing oxygenated water through permeable deltaic sediments in the former gravel pit area causes increases in dissolved oxygen concentrations and decreases in arsenic concentrations. Layered deltaic sediments produce anisotropic hydraulic characteristics and zones of high hydraulic conductivity. The glacial-sediment aquifer also includes glaciolacustrine sediments that have low permeability and limit infiltration at the surface Discharge of leachate-affected groundwater may be limited in areas of organic muck on the bottom of Whispering Pines Pond because the muck may act as a semiconfining layer. Geophysical survey results were used to identify several areas with continuous beds of muck and an underlying highresistivity layer on top of a layer of low resistivity that may represent leachate-affected groundwater. The high-resistivity layer is likely groundwater associated with oxygenated recharge, which would cause arsenic to adsorb onto aquifer sediments and reduce concentrations of dissolved arsenic in groundwater. Surface and borehole geophysical data collected in 2011 were used to identify potentially high-permeability or contaminated zones in the aquifer (preferential flowpaths) as well as low-permeability zones that may promote contamination through back diffusion. Some groundwater in parts of the glacial-sediment aquifer where the leachate plumes

Dissolved atmospheric gas in xylem sap measured with membrane inlet mass spectrometry.

Science.gov (United States)

Schenk, H Jochen; Espino, Susana; Visser, Ate; Esser, Bradley K

2016-04-01

A new method is described for measuring dissolved gas concentrations in small volumes of xylem sap using membrane inlet mass spectrometry. The technique can be used to determine concentrations of atmospheric gases, such as argon, as reported here, or for any dissolved gases and their isotopes for a variety of applications, such as rapid detection of trace gases from groundwater only hours after they were taken up by trees and rooting depth estimation. Atmospheric gas content in xylem sap directly affects the conditions and mechanisms that allow for gas removal from xylem embolisms, because gas can dissolve into saturated or supersaturated sap only under gas pressure that is above atmospheric pressure. The method was tested for red trumpet vine, Distictis buccinatoria (Bignoniaceae), by measuring atmospheric gas concentrations in sap collected at times of minimum and maximum daily temperature and during temperature increase and decline. Mean argon concentration in xylem sap did not differ significantly from saturation levels for the temperature and pressure conditions at any time of collection, but more than 40% of all samples were supersaturated, especially during the warm parts of day. There was no significant diurnal pattern, due to high variability between samples. © 2015 John Wiley & Sons Ltd.

Groundwater flow and its effect on salt dissolution in Gypsum Canyon watershed, Paradox Basin, southeast Utah, USA

Science.gov (United States)

Reitman, Nadine G.; Ge, Shemin; Mueller, Karl

2014-09-01

Groundwater flow is an important control on subsurface evaporite (salt) dissolution. Salt dissolution can drive faulting and associated subsidence on the land surface and increase salinity in groundwater. This study aims to understand the groundwater flow system of Gypsum Canyon watershed in the Paradox Basin, Utah, USA, and whether or not groundwater-driven dissolution affects surface deformation. The work characterizes the groundwater flow and solute transport systems of the watershed using a three-dimensional (3D) finite element flow and transport model, SUTRA. Spring samples were analyzed for stable isotopes of water and total dissolved solids. Spring water and hydraulic conductivity data provide constraints for model parameters. Model results indicate that regional groundwater flow is to the northwest towards the Colorado River, and shallow flow systems are influenced by topography. The low permeability obtained from laboratory tests is inconsistent with field observed discharges, supporting the notion that fracture permeability plays a significant role in controlling groundwater flow. Model output implies that groundwater-driven dissolution is small on average, and cannot account for volume changes in the evaporite deposits that could cause surface deformation, but it is speculated that dissolution may be highly localized and/or weaken evaporite deposits, and could lead to surface deformation over time.

Characterization of groundwater composition in Punjab state with special emphasis on uranium content, speciation and mobility

Energy Technology Data Exchange (ETDEWEB)

Kumar, Ajay; Rout, Sabyasachi; Mishra, Manish K.; Ravi, P.M. [Bhabha Atomic Reseach Centre, Mumbai (India). Health Physics Div.; Tripathi, R.M. [Bhabha Atomic Reseach Centre, Mumbai (India). Environmental Assessment Div.; Ghosh, A.K. [Bhabha Atomic Reseach Centre, Mumbai (India). Health, Safety and Environmental Group

2014-04-01

Groundwaters (borewell and handpump) were sampled from two districts (Bathinda and Mansa) of Punjab state and analyzed for their major ionic concentrations and uranium isotope compositions in order to assess the possible origins of the waters and water-rock interactions that occurred in the deep aquifer system. The major ionic concentrations of waters were plotted on a Piper diagram and grouped into four dominant hydrochemical facies as (Na+K)-SO{sub 4}+Cl type (69%-73%), (Ca+Mg)-SO{sub 4}+Cl type (6% - 21%), (Ca+Mg)-HCO{sub 3} type (4% - 6%) and (Na+K)-HCO{sub 3} type (2% - 19%). It was observed that mobility of uranium in groundwater was very much influenced by TDS (total dissolved solids). To investigate the various mechanisms for deriving the elevated uranium concentrations in groundwater, {sup 234}U/{sup 238}U activity ratios (ARs) were calculated using the determined activity levels of {sup 234}U and {sup 238}U. The mean ARs was found to be near unity (i.e. secular equilibrium) in the study regions confirmed that uranium in groundwaters was mainly resulted from its host/parent rocks through weathering processes. The concentration of HCO{sub 3}{sup -} in ground water showed one order of magnitude higher than the total dissolved SiO{sub 2} indicates that carbonate weathering was the dominant process due to major water-rock interaction. The uranium speciation in groundwaters was investigated by an equilibrium model calculation using MEDUSA (make equilibrium diagrams using sophisticated algorithms) under the influence of redox conditions and complexant concentration. At the observed range of pH values, the predominant redox speciation of uranium was observed as hydroxo-carbonato complexes of (UO{sub 2}){sub 2}(CO{sub 3})(OH){sub 3}{sup -} and hydroxyl complexes of UO{sub 2}(OH){sub 3}{sup -} which might be caused for increasing the solubility of uranium. Due to very low concentration of phosphate in groundwater, its effects on U(VI)-aqueous speciation was

Effects of groundwater-flow paths on nitrate concentrations across two riparian forest corridors

Science.gov (United States)

Speiran, Gary K.

2010-01-01

Groundwater levels, apparent age, and chemistry from field sites and groundwater-flow modeling of hypothetical aquifers collectively indicate that groundwater-flow paths contribute to differences in nitrate concentrations across riparian corridors. At sites in Virginia (one coastal and one Piedmont), lowland forested wetlands separate upland fields from nearby surface waters (an estuary and a stream). At the coastal site, nitrate concentrations near the water table decreased from more than 10 mg/L beneath fields to 2 mg/L beneath a riparian forest buffer because recharge through the buffer forced water with concentrations greater than 5 mg/L to flow deeper beneath the buffer. Diurnal changes in groundwater levels up to 0.25 meters at the coastal site reflect flow from the water table into unsaturated soil where roots remove water and nitrate dissolved in it. Decreases in aquifer thickness caused by declines in the water table and decreases in horizontal hydraulic gradients from the uplands to the wetlands indicate that more than 95% of the groundwater discharged to the wetlands. Such discharge through organic soil can reduce nitrate concentrations by denitrification. Model simulations are consistent with field results, showing downward flow approaching toe slopes and surface waters to which groundwater discharges. These effects show the importance of buffer placement over use of fixed-width, streamside buffers to control nitrate concentrations.

The use of carbon isotopes in the study of groundwater of the Bambui calcareous-central region of Bahia (Brazil)

International Nuclear Information System (INIS)

Cabral, F.C.F.

1978-06-01

Groundwater of 34 wells and of a spring of the Bambui limestone aquifer, in central Bahia, Brazil, were analized for the 14 C and 13 C content. One sample of soil CO 2 and four of soil organic matter were analized for 13 C. From these data were calculated the 14 C ages of these waters. A major difficulty in the use of radiocarbon in groundwater hydrology is the estimation of the initial 14 C concentration. In many cases, this can be simply determined by the fraction of carbon derived from soil gas, relative to the total carbon dissolved, by the use of Δ 13 C of the soil organic matter, limestone and dissolved carbon in water. This approach does not seem to be completely valid in arid ou semi-arid regions, specially where the pH of the soil is relatively high. In this case, the isotopic composition of the soil water can be determined if the pCO 2 and pH of the soil can be estimated and if the isotopic composition of the soil CO 2 can be known. The final isotopic composition of the groundwater is a combination of the isotopic composition of the soil water and any limestone thereafter dissolved. The 14 C ages of the water samples analized ranged from modern to about 13000 years. The recharge areas of the aquifer are clearly indicated, as the probable underground flow directions. The interpretation of the radiocarbon data is in accord with the hydrologic data. (Author) [pt

Contaminated groundwater characterization at the Chalk River Laboratories, Ontario, Canada

Energy Technology Data Exchange (ETDEWEB)

Schilk, A.J.; Robertson, D.E.; Thomas, C.W.; Lepel, E.A. [Pacific Northwest National Lab., Richland, WA (United States); Champ, D.R.; Killey, R.W.D.; Young, J.L.; Cooper, E.L. [Chalk River Labs., Chalk River, Ontario (Canada)

1993-03-01

The licensing requirements for the disposal of low-level radioactive waste (10 CFR 61) specify the performance objectives and technical requisites for federal and commercial land disposal facilities, the ultimate goal of which is to contain the buried wastes so that the general population is adequately protected from harmful exposure to any released radioactive materials. A major concern in the operation of existing and projected waste disposal sites is subterranean radionuclide transport by saturated or unsaturated flow, which could lead to the contamination of groundwater systems as well as uptake by the surrounding biosphere, thereby directly exposing the general public to such materials. Radionuclide transport in groundwater has been observed at numerous commercial and federal waste disposal sites [including several locations within the waste management area of Chalk River Laboratories (CRL)], yet the physico-chemical processes that lead to such migration are still not completely understood. In an attempt to assist in the characterization of these processes, an intensive study was initiated at CRL to identify and quantify the mobile radionuclide species originating from three separate disposal sites: (a) the Chemical Pit, which has received aqueous wastes containing various radioisotopes, acids, alkalis, complexing agents and salts since 1956, (b) the Reactor Pit, which has received low-level aqueous wastes from a reactor rod storage bay since 1956, and (c) the Waste Management Area C, a thirty-year-old series of trenches that contains contaminated solid wastes from CRL and various regional medical facilities. Water samples were drawn downgradient from each of the above sites and passed through a series of filters and ion-exchange resins to retain any particulate and dissolved or colloidal radionuclide species, which were subsequently identified and quantified via radiochemical separations and gamma spectroscopy. These groundwaters were also analyzed for anions

Iodine-129 and Iodine-127 speciation in groundwater at the Hanford Site, U.S.: iodate incorporation into calcite

International Nuclear Information System (INIS)

Zhang, Saijin; Yeager, Chris; Wellman, Dawn M.; Santschi, Peter H.

2013-01-01

The Hanford Site, the most contaminated nuclear site in the United States, has large radioactive waste plumes containing high 129I levels. The geochemical transport and fate of radioiodine depends largely on its chemical speciation that is greatly affected by environmental factors. This study reports, for the first time, the speciation of stable and radioactive iodine in the groundwater from the Hanford Site. Iodate was the dominant species and accounts for up to 84%, followed by organo-iodine and minimal levels of iodide. The relatively high pH and oxidizing environment may have prevented iodate reduction. Our results identified that calcite precipitation caused by degassing of CO2 during deep groundwater sampling incorporated between 7 to 40% of dissolved iodine (including 127I and 129I) that was originally in the groundwater, transforming dissolved to particulate iodate during sampling. In order to understand the mechanisms underlying iodine incorporation by calcite, laboratory experiments were carried out to replicate this iodine sequestering processes. Two methods were utilized in this study, 1) addition of sodium carbonate; 2) addition of calcium chloride followed by sodium carbonate where the pH was well controlled at ~8.2, which is close to the average pH of Hanford Site groundwater. It was demonstrated that iodate was the main species incorporated into calcite and this incorporation process could be impeded by elevated pH and decreasing ionic strength in groundwater. This study provides critical information for predicting the long-term fate and transport of 129I at the Hanford Site and reveals a potential means for improved remediation strategies of 129I

Geochemical modelling of groundwater evolution and residence time at the Olkiluoto site

International Nuclear Information System (INIS)

Pitkaenen, P.; Luukkonen, A.; Ruotsalainen, P.; Leino-Forsman, H.; Vuorinen, U.

1999-05-01

An understanding of the geochemical evolution of groundwater is an essential part of the performance assessment and safety analysis of the final disposal of radioactive waste into the bedrock. The performance of technical barriers and migration of possibly released radionuclides depend on chemical conditions. A prerequisite for understanding these factors is the ability to specify the water-rock interactions which control chemical conditions in groundwater. The objective of this study is to interpret the processes and factors which control the hydrogeochemistry, such as pH and redox conditions. A model of the hydrogeochemical progress in different parts of the crystalline bedrock at Olkiluoto has been created and the significance of chemical reactions and groundwater mixing along different flowpaths calculated. Long term hydrodynamics have also been evaluated. The interpretation and modelling are based on water samples (63 altogether) obtained from precipitation, Baltic Sea, soil layer, shallow wells in the bedrock, and eight deep boreholes in the bedrock for which a comprehensive data set on dissolved chemical species and isotopes was available. Some analyses of dissolved gases and fracture calcite and their isotopic measurements were also utilised. The data covers the bedrock at Olkiluoto to a depth of 1000 m. The results from groundwater chemistry, isotopes, petrography, hydrogeology of the site, geomicrobial studies, and PCA and speciation calculations were used in the evaluation of evolutionary processes at the site. The geochemical interpretation of water-rock interaction, isotope-chemical evolution and mixing of palaeo water types were approached by mass-balance calculations (NETPATH). Reaction-path calculations (EQ3/6) were used to verify the thermodynamic feasibility of the reaction models obtained. The interpretation and calculation of hydrochemical data from Olkiluoto reveals the complex nature of hydrogeochemical evolution at the site. Changes in

Geochemical modelling of groundwater evolution and residence time at the Olkiluoto site

Energy Technology Data Exchange (ETDEWEB)

Pitkaenen, P.; Luukkonen, A. [VTT Communities and Infrastructure, Espoo (Finland); Ruotsalainen, P. [Fintact Oy (Finland); Leino-Forsman, H.; Vuorinen, U. [VTT Chemical Technology, Espoo (Finland)

1999-05-01

An understanding of the geochemical evolution of groundwater is an essential part of the performance assessment and safety analysis of the final disposal of radioactive waste into the bedrock. The performance of technical barriers and migration of possibly released radionuclides depend on chemical conditions. A prerequisite for understanding these factors is the ability to specify the water-rock interactions which control chemical conditions in groundwater. The objective of this study is to interpret the processes and factors which control the hydrogeochemistry, such as pH and redox conditions. A model of the hydrogeochemical progress in different parts of the crystalline bedrock at Olkiluoto has been created and the significance of chemical reactions and groundwater mixing along different flowpaths calculated. Long term hydrodynamics have also been evaluated. The interpretation and modelling are based on water samples (63 altogether) obtained from precipitation, Baltic Sea, soil layer, shallow wells in the bedrock, and eight deep boreholes in the bedrock for which a comprehensive data set on dissolved chemical species and isotopes was available. Some analyses of dissolved gases and fracture calcite and their isotopic measurements were also utilised. The data covers the bedrock at Olkiluoto to a depth of 1000 m. The results from groundwater chemistry, isotopes, petrography, hydrogeology of the site, geomicrobial studies, and PCA and speciation calculations were used in the evaluation of evolutionary processes at the site. The geochemical interpretation of water-rock interaction, isotope-chemical evolution and mixing of palaeo water types were approached by mass-balance calculations (NETPATH). Reaction-path calculations (EQ3/6) were used to verify the thermodynamic feasibility of the reaction models obtained. The interpretation and calculation of hydrochemical data from Olkiluoto reveals the complex nature of hydrogeochemical evolution at the site. Changes in

Mechanisms of uranium interactions with hydroxyapatite: Implications for groundwater remediation

Science.gov (United States)

Fuller, C.C.; Bargar, J.R.; Davis, J.A.; Piana, M.J.

2002-01-01

The speciation of U(VI) sorbed to synthetic hydroxyapatite was investigated using a combination of U LIII-edge XAS, synchrotron XRD, batch uptake measurements, and SEM-EDS. The mechanisms of U(VI) removal by apatite were determined in order to evaluate the feasibility of apatitebased in-situ permeable reactive barriers (PRBs). In batch U(VI) uptake experiments with synthetic hydroxyapatite (HA), near complete removal of dissolved uranium (>99.5%) to use in development of PRBs for groundwater U(VI) remediation.

The evolution of redox conditions and groundwater geochemistry in recharge-discharge environments on the Canadian Shield

International Nuclear Information System (INIS)

Gascoyne, M.

1996-10-01

Groundwater composition evolves along flow paths from recharge to discharge in response to interactions with bedrock and fracture-filling minerals, and dissolution of soluble (Cl-rich) salts in the rock matrix. The groundwater redox potential changes from oxidizing to reducing conditions due, initially, to rapid consumption of dissolved oxygen by organics in the upper ∼100 m of bedrock and, subsequently, interaction with Fe (II)-containing minerals. Measured Eh values of groundwaters at depth in the granitic Lac du Bonnet batholith indicate that biotite and chlorite control groundwater redox potential. This is supported by other geochemical characteristics such as absence of CH 4 , H 2 S, H 2 , NO 3 , low concentrations of Fe (II), and abundance of SO 4 . Further evidence of evolution of redox conditions is given by variations in U concentration ranging from up to 1000 μg/L in dilute near-surface waters to <1 μg/L in some deep, saline groundwaters. Groundwaters at about 400 m depth in a recharge area on the Lac du Bonnet batholith contain significantly more U than groundwaters further along the flow path or near surface in discharge areas. Uranium concentration is found to be a useful and sensitive indicator of redox conditions. (author)

Shallow groundwater quality and geochemistry in the Fayetteville Shale gas-production area, north-central Arkansas, 2011

Science.gov (United States)

Kresse, Timothy M.; Warner, Nathaniel R.; Hays, Phillip D.; Down, Adrian; Vengosh, Avner; Jackson, Robert B.

2012-01-01

analyses. Additionally, no statistical difference existed between chloride concentrations from water-quality data collected for this study from 94 wells located less than 2 miles from a gas-production well and 33 wells located 2 miles or more from a gas-production well; a Wilcoxon rank-sum test showed a p-value of 0.71. Major ion chemistry was investigated to understand the effects of geochemical and reduction-oxidation (redox) processes on the shallow groundwater in the study area along a continuum of increased rock-water interaction represented by increases in dissolved solids concentration. Groundwater in sandstone formations is represented by a low dissolved solids concentration (less than 30 mg/L) and slightly acidic water type. Shallow shale aquifers were represented by dissolved solids concentrations ranging upward to 686 mg/L, and water types evolving from a dominantly mixed-bicarbonate and calcium-bicarbonate to a strongly sodium-bicarbonate water type. Methane concentration and carbon isotopic composition were analyzed in 51 of the 127 samples collected for this study. Methane occurred above a detection limit of 0.0002 mg/L in 32 of the 51 samples, with concentrations ranging upward to 28.5 mg/L. Seven samples had methane concentrations greater than or equal to 0.5 mg/L. The carbon isotopic composition of these higher concentration samples, including the highest concentration of 28.5 mg/L, shows the methane was likely biogenic in origin with carbon isotope ratio values ranging from -57.6 to -74.7 per mil. Methane concentrations increased with increases in dissolved solids concentrations, indicating more strongly reducing conditions with increasing rock-water interaction in the aquifer. As such, groundwater-quality data collected for this study indicate that groundwater chemistry in the shallow aquifer system in the study area is a result of natural processes, beginning with recharge of dilute atmospheric precipitation and evolution of observed groundwater

Development of a groundwater monitoring system at Horonobe Underground Research Center

International Nuclear Information System (INIS)

Nanjo, Isao; Amano, Yuki; Iwatsuki, Teruki; Murakami, Hiroaki; Kunimaru, Takanori; Morikawa, Keita; Hosoya, Shinichi

2012-03-01

Japan Atomic Energy Agency (JAEA) develops basic investigation techniques for deep geological environment around Underground Research Laboratory (URL) at Horonobe area, Japan. The observation technique of hydrochemical condition in low permeable sedimentary rock around the facility is one of R and D subjects. We report, 1) development of hydrochemical monitoring system to observe water pressure, pH, electric conductivity, dissolved oxygen, redox potential and temperature, 2) hydrochemical observation results around URL under construction. The applicability of the hydrochemical monitoring system is evaluated for low permeable sedimentary rock bearing abundant dissolved gases. The hydrochemical observation during facility construction demonstrates that pH and redox potential of groundwater almost did not changed even at hydraulic disturbed zone (water pressure decreased zone). A CD-ROM is attached as an appendix. (J.P.N.)

Water quality analysis of groundwater in crystalline basement rocks, Northern Ghana

Science.gov (United States)

Anku, Y.S.; Banoeng-Yakubo, B.; Asiedu, D.K.; Yidana, S.M.

2009-01-01

Hydrochemical data are presented for groundwater samples, collected from fractured aquifers in parts of northern Ghana. The data was collected to assess the groundwater suitability for domestic and agricultural use. Results of the study reveal that the pH of the groundwater in the area is slightly acidic to slightly alkaline. The electrical conductivity values, total dissolved solids (TDS) values and calcium, magnesium and sodium concentrations in the groundwater are generally below the limit set by the WHO for potable water supply. On the basis of activity diagrams, groundwater from the fractured aquifers appears to be stable within the montmorillonite field, suggesting weathering of silicate minerals. An inverse distance weighting interpolator with a power of 2 was applied to the data points to produce prediction maps for nitrate and fluoride. The distribution maps show the presence of high nitrate concentrations (50-194??mg/l) in some of the boreholes in the western part of the study area indicating anthropogenic impact on the groundwater. Elevated fluoride level (1.5-4??mg/l), higher than the WHO allowable fluoride concentration of 1.5, is recorded in the groundwater underlying the northeastern part of the study area, more specifically Bongo and its surrounding communities of the Upper East region. Results of this study suggest that groundwater from the fractured aquifers in the area exhibit low sodicity-low salinity (S1-C1), low sodicity-medium salinity (S1-C2) characteristics [United States Salinity Laboratory (USSL) classification scheme]. All data points from this study plot within the 'Excellent to good' category on a Wilcox diagram. Groundwater in this area thus appears to provide irrigation water of excellent quality. The hydrochemical results indicate that, although nitrate and fluoride concentrations in some boreholes are high, the groundwater in the study area, based on the parameters analyzed, is chemically potable and suitable for domestic and

Remediation of arsenic-contaminated groundwater by in-situ stimulating biogenic precipitation of iron sulfides.

Science.gov (United States)

Pi, Kunfu; Wang, Yanxin; Xie, Xianjun; Ma, Teng; Liu, Yaqing; Su, Chunli; Zhu, Yapeng; Wang, Zhiqiang

2017-02-01

Severe health problems due to elevated arsenic (As) in groundwater have made it urgent to develop cost-effective technologies for As removal. This field experimental study tested the feasibility of in-situ As immobilization via As incorporation into newly formed biogenic Fe(II) sulfides in a typical As-affected strongly reducing aquifer at the central part of Datong Basin, China. After periodic supply of FeSO 4 into the aquifer for 25 d to stimulate microbial sulfate reduction, dissolved sulfide concentrations increased during the experiment, but the supplied Fe(II) reacted quickly with sulfide to form Fe(II)-sulfides existing majorly as mackinawite as well as a small amount of pyrite-like minerals in sediments, thereby restricting sulfide build-up in groundwater. After the completion of field experiment, groundwater As concentration decreased from an initial average value of 593 μg/L to 159 μg/L, with an overall As removal rate of 73%, and it further declined to 136 μg/L adding the removal rate up to 77% in 30 d after the experiment. The arsenite/As total ratio gradually increased over time, making arsenite to be the predominant species in groundwater residual As. The good correlations between dissolved Fe(II), sulfide and As concentrations, the increased abundance of As in newly-formed Fe sulfides as well as the reactive-transport modeling results all indicate that As could have been adsorbed onto and co-precipitated with Fe(II)-sulfide coatings once microbial sulfate reduction was stimulated after FeSO 4 supply. Under the strongly reducing conditions, sulfide may facilitate arsenate reduction into arsenite and promote As incorporation into pyrite or arsenopyrite. Therefore, the major mechanisms for the in-situ As-contaminated groundwater remediation can be As surface-adsorption on and co-precipitation with Fe(II) sulfides produced during the experimental period. Copyright © 2016. Published by Elsevier Ltd.

Electron Shuttling by Dissolved Humic Substances: Using Fluorescence Spectroscopy to Move Beyond the Laboratory to Natural Lakes, Streams and Groundwaters

Science.gov (United States)

McKnight, D. M.

2017-12-01

Humic substances are an important class of reactive chemical species in natural waters, and one important role is their capacity to as an electron acceptor and/or electron shuttle to ferric iron present as solid phase ferric oxides. Several lines of evidence point to quinone-like moieties being the main redox active moieties that can be used by microbes in respiration. Concomitantly, the humic fraction of dissolved organic mater (DOM) contains the dominant fluorophores in many natural waters. Examination of excitation emission matrices (EEMs) across redox gradients in diverse aquatic systems show that the EEMs are generally red-shifted under reducing conditions, such as anoxic bottom waters in lakes and hypoxic waters in riparian wetlands. Furthermore, there is striking similarity between the humic fluorophores that are resolved by statistical analysis and the fluorescence spectra of model quinone compounds, with the more reduced species having red-shifted fluorescence spectra. This apparent red-shift can be quantified based on the distribution of apparently "quinone-like", "semi-quinone-like" and "hydroquinone-like" fluorophores determined by the PARAFAC statistical analysis. Because fluorescence spectroscopy can be applied at ambient DOM concentrations for samples that have been maintained in an anoxic condition, fluorescence spectroscopy can provide insight into the role of humic electron shuttling in natural systems. Examples are presented demosntrating the changing EEMs in anoxic bottomwaters in a lake in the McMurdo Dry Valleys following a major flood event and the role of organic material in the mobilization of arsenic in shallow groundwater in South East Asia.

Biodegradation of cyanide in groundwater and soils from gasworks sites in south-eastern Australia

Energy Technology Data Exchange (ETDEWEB)

Meehan, S.M.E.; Weaver, T.R.; Lawrence, C.R. [University of Melbourne, Parkvills, Vic. (Australia). School of Earth Sciences

1999-07-01

Groundwater from a gasworks site in south-eastern Australia has been found to contain high concentrations of cyanide (total), sulphate, and ammonia (1400 mg L{sup -1}, 6500 mg L{sup -1}, and 580 mg L{sup -1} respectively). Soil from another gasworks site has been found to contain 587 mg kg{sup -1} of cyanide (total), with concentrations of cyanide in the groundwater at this site being relatively low ({lt} 21 mgL{sup -1} CN(Total)). Experiments were conducted to determine the biodegradation rates of cyanide in groundwater and soils using samples from both sites. Column experiments and bioreactors were constructed to produce both aerobic and anaerobic conditions for the groundwater containing high concentrations of cyanide. Samples of water were taken periodically to analyse the pH, redox potential, temperature, and concentrations of cyanide (free and total), sulphate, ammonia, nitrate and dissolved organic carbon (DOC). Initial results indicate that concentrations of cyanide are declining in both aerobic and anaerobic conditions, with biodegradation one process producing degradation. 9 refs., 4 figs., 2 tabs.

Influence of volcanic history on groundwater patterns on the west slope of the Oregon High Cascades.

Science.gov (United States)

A. Jefferson; G. Grant; T. Rose

2006-01-01

Spring systems on the west slope of the Oregon High Cascades exhibit complex relationships among modern topography, lava flow geometries, and groundwater flow patterns. Seven cold springs were continuously monitored for discharge and temperature in the 2004 water year, and they were periodically sampled for ?18O, ?D, tritium, and dissolved noble gases. Anomalously high...

Arsenic mobility in groundwater/surface water systems in carbonate-rich Pleistocene glacial drift aquifers (Michigan)

International Nuclear Information System (INIS)

Szramek, Kathryn; Walter, Lynn M.; McCall, Patti

2004-01-01

waters have very low As and Fe contents, consistent with the stability of oxyhydroxides under oxidizing vadose conditions. When CO 2 charged groundwaters discharge in streams and fens, dissolved As is effectively removed by adsorption onto Fe-oxides or carbonate marls. Although Fe does not display conservative behavior with As in groundwaters, a strong positive correlation exists between As and Sr concentrations. As water-rock interactions proceed, the As/Fe and Sr/Ca ratios would be expected to increase because both As and Sr behave as incompatible elements. Comparisons with groundwater chemistries from other drift-hosted aquifers proximate to the Marshall sandstone are consistent with these relations. Thus, the Sr content of carbonate-rich groundwaters may provide useful constraints on the occurrence, origin and evolution of dissolved As in such systems

Monitoring report of groundwater quality around the Yotsugi mill-tailings dam, Ningyo-toge, Okayama, Japan

International Nuclear Information System (INIS)

Matsumura, Toshihiro; Takeuchi, Akira; Sato, Kazuhiko; Tsurudome, Koji; Tokizawa, Takayuki

1999-08-01

Monitoring of groundwater quality from boreholes around the Yotsugi mill-tailings dam, in the Ningyo-toge Environmental Engineering Center, JNC, have been carried out to estimate extent and quality of contaminated water plume from the mill-tailings pile. In this report, data collected from 1979 to 1998 fiscal year were listed and their spatial and time variation of physicochemical parameters, uranium and radium were also summarized. Additionally, groundwater sampler has been improved and analytical method has been modified. Some results from groundwater quality were; 1. Uranium and radium concentrations were low, although unexpected change was appeared in some borehole. 2. Water table and temperature from boreholes on the left bank of the dam showed drastically change. 3. Electric conductivity and concentrations or various dissolved ions tend to high from the embankment upward, whereas they tend to low from the embankment downward. (author)

Regional distribution of microbes in groundwater from Haestholmen, Kivetty, Olkiluoto and Romuvaara, Finland

Energy Technology Data Exchange (ETDEWEB)

Haveman, S.A.; Nilsson, E.L.; Pedersen, K. [Goeteborg University (Sweden)

2000-06-01

Groundwater was sampled with the PAVE groundwater sampling system from eight boreholes at Haestholmen, Kivetty, Olkiluoto and Romuvaara, Finland, in 1998 and 1999, for investigation of microbial populations. The groundwater samples had a wide range of salinity and chemistry and contained 104-105 cells per ml, which is typical for subsurface groundwater. In preparing culture media, two approaches were used and compared. Natural, groundwater-based media were prepared from groundwater from the same section of each borehole tested, and synthetic media were prepared based on groundwater chemistry data. No significant difference was observed between the two types of media for brackish and saline groundwater. The groundwater to a depth of 750 m contained mainly sulphate-reducing bacteria (SRB), ironreducing bacteria (IRB) and heterotrophic acetogenic (HA) bacteria. Autotrophic acetogenic (AA) bacteria and methanogenic archaea were found in some samples. Iron-reducing and HA bacteria predominated in brackish groundwater from Haestholmen, with SRB present in smaller numbers. A different microbial population was found in deep saline groundwater from Haestholmen and Olkiluoto that consists of a large proportion of a saline or brine end member. No SRB or AA bacteria were cultured; instead, the microbial population consisted of HA bacteria and either IRB or methanogens. In Olkiluoto, SRB predominated in the brackish and saline groundwater at depths to about 500 m, while methanogens were found in deeper saline groundwater. Stable isotope data (C-13) indicated that the methanogens are part of an autotrophic population consuming dissolved inorganic carbon (DIC) and hydrogen and producing methane and organic carbon. This deep ecosystem may be independent of surface life processes. A high-level radioactive waste (HLW) repository at 500 m depth in the Fennoscandian Shield will be inhabited by SRB, IRB and acetogens. Methanogens may also be present. These anaerobic micro

Identification of manganese as a toxicant in a groundwater treatment system: Addressing naturally occurring toxicants

International Nuclear Information System (INIS)

Goodfellow, W. Jr.; Sohn, V.; Richey, M.; Yost, J.

1995-01-01

Effluent from a groundwater remediation system at a bulk oil storage and distribution terminal has been chronically toxic to Ceriodaphnia dubia. The remediation system was designed in response to a hydrocarbon plume in the area of the terminal. The remediation system consists of a series of groundwater recovery wells and groundwater intercept trench systems with groundwater treatment and phased-separated hydrocarbon recovery systems. The groundwater treatment and petroleum recovery systems consist of oil/water separators, product recovery tanks, air strippers, filters, and carbon adsorption units. The characteristics of this effluent are low total suspended solids, total dissolved solids, and hardness concentrations as well as meeting stringent NPDES permit requirements for lead, copper, zinc, mercury, total petroleum hydrocarbons, and BTEX. Additional priority pollutant evaluations revealed no compounds of concern. Performance of a Toxicity identification Evaluation (TIE) indicated that manganese was the principle toxicant in the effluent. Manganese is a naturally occurring constituent in this groundwater source and is not added to the treatment system. This paper will present the results of the TIE with a discussion of treatability/control options for manganese control at this facility. Recommendations for addressing naturally occurring toxicants that are not a result of the facility's operations will also be presented

Thorium coprecipitation method for spectrophotometric determination of arsenic (III) and arsenic (V) in groundwaters

International Nuclear Information System (INIS)

Tamari, Yuzo; Yamamoto, Nobuki; Tsuji, Haruo; Kusaka, Yuzuru

1989-01-01

A new coprecipitation method for the spectrophotometry of arsenic (III) and arsenic (V) in groundwater has been developed. Arsenic (III) and arsenic (V) were coprecipitated with thorium (IV) hydroxide from 1000ml of groundwater at pH9. The precipitate was centrifuged and then dissolved with hydrochloric acid. Arsenic (III) was spectrophotometrically determined by the usual silver diethylditiocarbamate (Ag-DDTC) method after generating the arsenic to arsine with sodium tetrahydroborate under masking the thorium with EDTA-NaF at pH6. From another portion of the same groundwater, both arsenic (III) and arsenic (V) were determined by the Ag-DDTC method after reducing all the arsenic to arsine with sodium tetrahydroborate at pH less than 1 in the presence of the EDTA-NaF. The concentration of arsenic (V) was obtained by subtracting that of arsenic (III) from the total for arsenic. (author)

Dissolved inorganic carbon and organic carbon in mires in the Forsmark area. A pilot study

Energy Technology Data Exchange (ETDEWEB)

Loefgren, Anders [EcoAnalytica, Haegersten (Sweden)

2011-12-15

Dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC) are the large dissolved carbon pools in mires. They are both related to a number of factors such as groundwater flow, minerogenic influence and peat properties, which all are more or less related to peatland development stage. In a scenario of a release of radionuclides from an underground repository containing radioactive material, behaviour of these pools during the mire ontogeny will be of importance for the understanding of how C-14 will constitute a potential risk to humans and non-human biota. In this pilot study, DIC and DOC concentrations were investigated for three mires representing a potential sequence of peatland development in a coastal area at Forsmark in central Sweden characterized by land upheaval, a flat topography and calcareous content in the soil. The mires where chosen based on difference in height above the sea level, covering approximate 1000 years, and characteristics based on their vegetation. Water samples were collected during August from all three mires at two different depths in the anoxic layer of the mires, by extracting water from peat obtained with a peat corer. DIC concentrations where related to the age of the mires, with the lowest concentrations in the highest located mire. There was a positive correlation between pH and DIC, where the higher DIC concentrations were found in the 'richer' fens. DIC concentrations were also positively related to the conductivity within and between the mires, where conductivity would be a proxy for the dominating cation Ca{sup 2+} associated to the calcareous-influenced groundwater. DOC concentrations were highest in the oldest mire, but were similar in the younger mires. No patterns were found between DIC and DOC, and the peat bulk density. The report ends with suggestions on how a continued study could be improved.

Dissolved inorganic carbon and organic carbon in mires in the Forsmark area. A pilot study

International Nuclear Information System (INIS)

Loefgren, Anders

2011-12-01

Dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC) are the large dissolved carbon pools in mires. They are both related to a number of factors such as groundwater flow, minerogenic influence and peat properties, which all are more or less related to peatland development stage. In a scenario of a release of radionuclides from an underground repository containing radioactive material, behaviour of these pools during the mire ontogeny will be of importance for the understanding of how C-14 will constitute a potential risk to humans and non-human biota. In this pilot study, DIC and DOC concentrations were investigated for three mires representing a potential sequence of peatland development in a coastal area at Forsmark in central Sweden characterized by land upheaval, a flat topography and calcareous content in the soil. The mires where chosen based on difference in height above the sea level, covering approximate 1000 years, and characteristics based on their vegetation. Water samples were collected during August from all three mires at two different depths in the anoxic layer of the mires, by extracting water from peat obtained with a peat corer. DIC concentrations where related to the age of the mires, with the lowest concentrations in the highest located mire. There was a positive correlation between pH and DIC, where the higher DIC concentrations were found in the 'richer' fens. DIC concentrations were also positively related to the conductivity within and between the mires, where conductivity would be a proxy for the dominating cation Ca 2+ associated to the calcareous-influenced groundwater. DOC concentrations were highest in the oldest mire, but were similar in the younger mires. No patterns were found between DIC and DOC, and the peat bulk density. The report ends with suggestions on how a continued study could be improved

Variability of the groundwater sulfate concentration in fractured rock slopes: a tool to identify active unstable areas

Directory of Open Access Journals (Sweden)

S. Binet

2009-12-01

Full Text Available Water chemical analysis of 100 springs from the Orco and the Tinée valleys (Western Italy and Southern France and a 7 year groundwater chemistry monitoring of the 5 main springs were performed. All these springs drain from crystalline rock slopes. Some of these drain from currently active gravitational slope deformations.

All groundwaters flowing through presently unstable slopes show anomalies in the sulfate concentrations compared to stable aquifers. Particularly, an increase of sulfate concentrations was observed repeatedly after each of five consecutive landslides on the La Clapière slope, thus attesting to the mechanical deformations are at the origin of this concentration change. Significant changes in the water chemistry are produced even from slow (mm/year and low magnitude deformations of the geological settings.

Pyrite nuclei in open fractures were found to be coated by iron oxides. This suggests that the increase of dissolved sulfate relates to oxidative dissolution of Pyrite. Speciation calculations of Pyrite versus Gypsum confirmed that observed changes in the sulfate concentrations is predominantly provided from Pyrite. Calculated amounts of dissolved minerals in the springs water was obtained through inverse modelling of the major ion water analysis data. It is shown that the concentration ratio of calculated dissolved Pyrite versus calculated dissolved gneiss rock allows us to unambiguously distinguish water from stable and unstable areas. This result opens an interesting perspective for the follow-up of sliding or friction dynamic in landslides or in (a seismic faults.

Carbon dioxide degassing at the groundwater-stream-atmosphere interface: isotopic equilibration and hydrological mass balance in a sandy watershed

Science.gov (United States)

Deirmendjian, Loris; Abril, Gwenaël

2018-03-01

Streams and rivers emit significant amounts of CO2 and constitute a preferential pathway of carbon transport from terrestrial ecosystems to the atmosphere. However, the estimation of CO2 degassing based on the water-air CO2 gradient, gas transfer velocity and stream surface area is subject to large uncertainties. Furthermore, the stable isotope signature of dissolved inorganic carbon (δ13C-DIC) in streams is strongly impacted by gas exchange, which makes it a useful tracer of CO2 degassing under specific conditions. For this study, we characterized the annual transfers of dissolved inorganic carbon (DIC) along the groundwater-stream-river continuum based on DIC concentrations, stable isotope composition and measurements of stream discharges. We selected a homogeneous, forested and sandy lowland watershed as a study site, where the hydrology occurs almost exclusively through drainage of shallow groundwater (no surface runoff). We observed the first general spatial pattern of decreases in pCO2 and DIC and an increase in δ13C-DIC from groundwater to stream orders 1 and 2, which was due to the experimentally verified faster degassing of groundwater 12C-DIC compared to 13C-DIC. This downstream enrichment in 13C-DIC could be modelled by simply considering the isotopic equilibration of groundwater-derived DIC with the atmosphere during CO2 degassing. A second spatial pattern occurred between stream orders 2 and 4, consisting of an increase in the proportion of carbonate alkalinity to the DIC accompanied by the enrichment of 13C in the stream DIC, which was due to the occurrence of carbonate rock weathering downstream. We could separate the contribution of these two processes (gas exchange and carbonate weathering) in the stable isotope budget of the river network. Thereafter, we built a hydrological mass balance based on drainages and the relative contribution of groundwater in streams of increasing order. After combining with the dissolved CO2 concentrations, we

Petrol contaminated groundwater treatment with air-stripper in Balassagyarmat, Hungary

International Nuclear Information System (INIS)

Szabo, Peter; Bernath, Balazs

2005-01-01

Hydrocarbon contaminated groundwater is a common environmental problem in Hungary. Leakage of underground storage tanks, pipe break or illegal tapping as well as lorry accidents can be mentioned as main reasons. MEGATERRA Ltd. elaborated, adopted and tested several groundwater clean-up methods. These methods are based on detailed survey and investigation, sampling and analysis, delineation of contaminated groundwater, risk assessment, establishment of monitoring wells, pumping tests and remediation action plan. One of these methods was implemented by MEGATERRA Ltd. in Balassagyarmat, Hungary. Contamination source was a 10 m 3 vol. simple wall underground fuel-storage tank, which had been emptied. When the remediation started in April 1998, the petrol had already been accumulated on the ground water table forming a 5-7 m wide and 10-15 m long plume being expanded to SSE-NNW direction. The area of the dissolved hydrocarbon contaminated groundwater-body was 1 000 m 2 and its concentration reached up to 30-40 mg/l TPH. The free-phase hydrocarbon layer was 10 cm thick. For the remediation of contaminated groundwater MEGATERRA Ltd. applied pump and treat method, namely groundwater pumping using extraction well, skimming of free-phase hydrocarbon, stripping of the contaminated ground water in air-stripper tower and draining of the treated groundwater into a drainage ditch. In the centre of the plume we established an extraction well with 300 mm diameter in a 500 mm borehole. Peristaltic skimmer pump was used inside the extraction well to remove the free phase petrol from the ground water surface.Because of the intense volatility of the pollutant we applied aeration (stripping) technology. The extracted contaminated groundwater was cleaned in air-stripper equipment being able to eliminate efficiently the volatile pollutants from the water. The aeration tower is a compact cylindrical shaped column with 650 mm in diameter. Its height depends on the pollutant's type The

Trends in concentrations of nitrate and total dissolved solids in public supply wells of the Bunker Hill, Lytle, Rialto, and Colton groundwater subbasins, San Bernardino County, California: influence of legacy land use.

Science.gov (United States)

Kent, Robert; Landon, Matthew K

2013-05-01

Concentrations and temporal changes in concentrations of nitrate and total dissolved solids (TDS) in groundwater of the Bunker Hill, Lytle, Rialto, and Colton groundwater subbasins of the Upper Santa Ana Valley Groundwater Basin were evaluated to identify trends and factors that may be affecting trends. One hundred, thirty-one public-supply wells were selected for analysis based on the availability of data spanning at least 11 years between the late 1980s and the 2000s. Forty-one of the 131 wells (31%) had a significant (p<0.10) increase in nitrate and 14 wells (11%) had a significant decrease in nitrate. For TDS, 46 wells (35%) had a significant increase and 8 wells (6%) had a significant decrease. Slopes for the observed significant trends ranged from -0.44 to 0.91 mg/L/yr for nitrate (as N) and -8 to 13 mg/L/yr for TDS. Increasing nitrate trends were associated with greater well depth, higher percentage of agricultural land use, and being closer to the distal end of the flow system. Decreasing nitrate trends were associated with the occurrence of volatile organic compounds (VOCs); VOC occurrence decreases with increasing depth. The relations of nitrate trends to depth, lateral position, and VOCs imply that increasing nitrate concentrations are associated with nitrate loading from historical agricultural land use and that more recent urban land use is generally associated with lower nitrate concentrations and greater VOC occurrence. Increasing TDS trends were associated with relatively greater current nitrate concentrations and relatively greater amounts of urban land. Decreasing TDS trends were associated with relatively greater amounts of natural land use. Trends in TDS concentrations were not related to depth, lateral position, or VOC occurrence, reflecting more complex factors affecting TDS than nitrate in the study area. Published by Elsevier B.V.

Groundwater Quality Data in the Mojave Study Unit, 2008: Results from the California GAMA Program

Science.gov (United States)

Mathany, Timothy M.; Belitz, Kenneth

2009-01-01

Groundwater quality in the approximately 1,500 square-mile Mojave (MOJO) study unit was investigated from February to April 2008, as part of the Priority Basin Project of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The GAMA Priority Basin Project was developed in response to the Groundwater Quality Monitoring Act of 2001 and is being conducted by the U.S. Geological Survey (USGS) in cooperation with the California State Water Resources Control Board (SWRCB). MOJO was the 23rd of 37 study units to be sampled as part of the GAMA Priority Basin Project. The MOJO study was designed to provide a spatially unbiased assessment of the quality of untreated ground water used for public water supplies within MOJO, and to facilitate statistically consistent comparisons of groundwater quality throughout California. Samples were collected from 59 wells in San Bernardino and Los Angeles Counties. Fifty-two of the wells were selected using a spatially distributed, randomized grid-based method to provide statistical representation of the study area (grid wells), and seven were selected to aid in evaluation of specific water-quality issues (understanding wells). The groundwater samples were analyzed for a large number of organic constituents [volatile organic compounds (VOCs), pesticides and pesticide degradates, and pharmaceutical compounds], constituents of special interest (perchlorate and N-nitrosodimethylamine [NDMA]) naturally occurring inorganic constituents (nutrients, dissolved organic carbon [DOC], major and minor ions, silica, total dissolved solids [TDS], and trace elements), and radioactive constituents (gross alpha and gross beta radioactivity, radium isotopes, and radon-222). Naturally occurring isotopes (stable isotopes of hydrogen, oxygen, and carbon, stable isotopes of nitrogen and oxygen in nitrate, and activities of tritium and carbon-14), and dissolved noble gases also were measured to help identify the sources and ages of the sampled

Modeling of groundwater using the isotopic technique in the sedimentary aquifer of the Mahafaly basin, southwestern Madagascar

International Nuclear Information System (INIS)

Fareze, L.H.

2016-01-01

The Mahafaly sedimentary basin, southwest of Madagascar belongs to the region where the water resources management problem, such as high groundwater mineralization and dry wells lingers. In this research work, hydrochemistry and isotopes techniques are used to assess the groundwater characteristics, to determine the groundwater origin and to understand their geochemical evolution. The development of an hydrological model using Modflow software contribute to control the groundwater flow and predict the dissolved particles evolution and travel time according to their flow direction. Dissolution of halite, calcite and gypsum and cation exchange are the main sources of the groundwater mineralization in the study area. The groundwater isotopic composition indicates that the groundwaters are directly recharged by local precipitation, having a mean time of 25 years. A mixture of groundwater and Onilahy river water occurs in adjacent aquifers, of which residence time is about 60 years. A mixture of recent and old groundwaters by the upwelling of the deep waters is observed in the southern aquifer of Isalo, confirmed by the tritium concentration value, which is lower than 0,5UT. The model established indicates a high groundwater flow rate from the recharge area, located in Betioky hill. This is due to a steep slope with a hydraulic conductivity of about 10 -5 m.s -1 , although other flow directions have been identified. The model predicts a decrease of the hydraulic head during the last decades. [fr

New Zealand guidelines for the collection of groundwater samples for chemical and isotopic analyses

International Nuclear Information System (INIS)

Rosen, M.R.; Cameron, S.G.; Reeves, R.R.; Taylor, C.B.

1999-01-01

Chemical and isotopic analyses of groundwater are important tools for differentiating between the natural composition and human-induced contaminants of groundwater. A comprehensive suite of inorganic water chemical analyses is necessary to characterise waters. The geology of New Zealand is diverse, so it is impractical to characterise a ''typical'' groundwater chemical composition. Each aquifer system should be evaluated individually because the major dissolved species contain useful information about the pathways of water through the soil zone into the aquifer. Analyses of major ions such as chloride, nitrate, potassium and sulphate often give indication of septic systems and agricultural contamination. The minor ions, while most are not considered contaminants, are often indicators of human activity. Iron and manganese are good indicators of Eh potential, which is an important control on the mobility of many heavy metals. The inexpensive inorganic chemical analytical suite should be used as a guide to advisability of more expensive contaminant testing. The purpose of this manual is to provide consistent groundwater sampling guidelines for use throughout New Zealand. Sinton's (1998) guide to groundwater sampling techniques provided a sound basis for the accurate collection of groundwater samples. However Sinton did not address sampling materials and techniques for the collection of samples for ultra trace component analysis or the collection of environmental isotope samples. These important aspects of groundwater sampling have been included in this updated manual. (author). 30 refs., 12 figs., 5 tabs., 1 appendix

Appraisal of groundwater resources of Ziarat valley using isotopic techniques

International Nuclear Information System (INIS)

Ahmad, M.; Akram, W.; Tasneem, M.A.; Rafique, M.

2009-07-01

Study of water resources of Ziarat Valley was carried out to investigate groundwater recharge mechanism and effectiveness of delay action dams. Samples of precipitation (rain, snow), dam reservoirs and groundwater (dug wells, tube wells, karezes, springs) were periodically collected from different locations and analyzed for environmental isotopes (/sup 2/H, /sup 3/H, /sup 18/O, /sup 34/S). The data indicate that rainfall and snow samples show wide ranges of delta /sup 2/H and delta /sup 18/O. However, the mean values for these isotopes are -6.4% and -37% respectively. Mean tritium value of rain is 9TU. Delta /sup 2/H and delta /sup 18/O values of dam reservoirs range from -6.7 to +4.9% and -42 to +30% respectively. Average isotopic indices of all the karezes are close to each other. Mean delta /sup 18/O and delta /sup 2/H values of Sandaman Tangi, Faran Tangi and Quaid springs vary from -6.3 to -6% and -40 to -31%. Tritium concentration of Sandaman Tangi and Faran Tangi springs (7 TU) is less than Quaid spring (11TU). Ranges of mean delta /sup 18/O and delta /sup 2/H values of all the groundwater samples (wells, karezes, springs) are -6.6 to -2.2% and -40 to -16% respectively. Delta /sup 34/S values of dissolved sulphates in groundwater vary from -8.5 to -0.8%. In /sup 18/O vs. /sup 2/H plot, most of the groundwater samples lie close to LMWL indicating the meteoric origin. Reservoir water in Pechi Dam shows highly enriched isotopic values in summer due to evaporation. Such enriched values are not depicted by the groundwater in the wells and karezes downstream of the dam. This implies that there is no significant recharge from this dam. Similar is the case of Mana Dam. Vouch Ghouski Dam has some contribution towards groundwater recharge while Warchoom Dam is much effective and makes significant contribution. Results of tritium dating suggest that residence time of groundwater is quite short (only few years). (author)

In situ air sparging for bioremediation of groundwater and soils

International Nuclear Information System (INIS)

Lord, D.; Lei, J.; Chapdelaine, M.C.; Sansregret, J.L.; Cyr, B.

1995-01-01

Activities at a former petroleum products depot resulted in the hydrocarbon contamination of soil and groundwater over a 30,000-m 2 area. Site remediation activities consisted of three phases: site-specific characterization and treatability study, pilot-scale testing, and full-scale bioremediation. During Phase 1, a series of site/soil/waste characterizations was undertaken to ascertain the degree of site contamination and to determine soil physical/chemical and microbiological characteristics. Treatability studies were carried out to simulate an air sparging process in laboratory-scale columns. Results indicated 42% mineral oil and grease removal and 94% benzene, toluene, ethylbenzene, and xylenes (BTEX) removal over an 8-week period. The removal rate was higher in the unsaturated zone than in the saturated zone. Phase 2 involved pilot-scale testing over a 550-m 2 area. The radius of influence of the air sparge points was evaluated through measurements of dissolved oxygen concentrations in the groundwater and of groundwater mounding. A full-scale air sparging system (Phase 3) was installed on site and has been operational since early 1994. Physical/chemical and microbiological parameters, and contaminants were analyzed to evaluate the system performance

Particulate Pyrite Autotrophic Denitrification (PPAD) for Remediation of Nitrate-contaminated Groundwater

Science.gov (United States)

Tong, S.; Rodriguez-Gonzalez, L. C.; Henderson, M.; Feng, C.; Ergas, S. J.

2015-12-01

The rapid movement of human civilization towards urbanization, industrialization, and increased agricultural activities has introduced a large amount of nitrate into groundwater. Nitrate is a toxic substance discharged from groundwater to rivers and leads to decreased dissolved oxygen and eutrophication. For this experiment, an electron donor is needed to convert nitrate into non-toxic nitrogen gas. Pyrite is one of the most abundant minerals in the earth's crust making it an ideal candidate as an electron donor. The overall goal of this research was to investigate the potential for pyrite to be utilized as an electron donor for autotrophic denitrification of nitrate-contaminated groundwater. Batch studies of particulate pyrite autotrophic denitrification (PPAD) of synthetic groundwater (100 mg NO3--N L-1) were set up with varying biomass concentration, pyrite dose, and pyrite particle size. Reactors were seeded with mixed liquor volatile suspended solids (VSS) from a biological nitrogen removal wastewater treatment facility. PPAD using small pyrite particles (exhibited substantial nitrate removal rate, lower sulfate accumulation (5.46 mg SO42-/mg NO3--N) and lower alkalinity consumption (1.70 mg CaCO3/mg NO3--N) when compared to SOD (7.54 mg SO42-/mg NO3--N, 4.57 mg CaCO3/mg NO3--N based on stoichiometric calculation). This research revealed that the PPAD process is a promising technique for nitrate-contaminated groundwater treatment and promoted the utilization of pyrite in the field of environmental remediation.

Naturally occurring arsenic in the groundwater at the Kansas City Plant

Energy Technology Data Exchange (ETDEWEB)

Korte, N.E.

1990-12-01

This report describes an investigation concerning the presence of arsenic in concentrations exceeding 0.4 mg/L in the groundwater under the Department of Energy's Kansas City Plant (KCP). The study consisted of four distinct phases: a thorough review of the technical literature, a historical survey of arsenic use at the facility, a laboratory study of existing techniques for determining arsenic speciation, and a field program including water, soil, and sediment sampling. The historical survey and literature review demonstrated that plant activities had not released significant quantities of arsenic to the environment but that similar occurrences of arsenic in alluvial groundwater are widespread in the midwestern United States. Laboratory studies showed that a chromatographic separation technique was necessary to accurately determine arsenic speciation for the KCP groundwater samples. Field studies revealed that naturally occurring reducing conditions prevalent in the subsurface are responsible for dissolving arsenic previously sorbed by iron oxides. Indeed, the data demonstrated that the bulk arsenic concentration of site subsoils and sediments is {approximately}7 mg/kg, whereas the arsenic content of iron oxide subsamples is as high as 84 mg/kg. Literature showed that similar concentrations of arsenic in sediments occur naturally and are capable of producing the levels of arsenic found in groundwater monitoring wells at the KCP. The study concludes, therefore, that the arsenic present in the KCP groundwater is the result of natural phenomena. 44 refs., 8 figs., 14 tabs.

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

Science.gov (United States)

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.

Concentrations and speciation of arsenic along a groundwater flow-path in the Upper Floridan aquifer, Florida, USA

Science.gov (United States)

Haque, S. E.; Johannesson, K. H.

2006-05-01

Arsenic (As) concentrations and speciation were determined in groundwaters along a flow-path in the Upper Floridan aquifer (UFA) to investigate the biogeochemical “evolution“ of As in this relatively pristine aquifer. Dissolved inorganic As species were separated in the field using anion-exchange chromatography and subsequently analyzed by inductively coupled plasma mass spectrometry. Total As concentrations are higher in the recharge area groundwaters compared to down-gradient portions of UFA. Redox conditions vary from relatively oxic to anoxic along the flow-path. Mobilization of As species in UFA groundwaters is influenced by ferric iron reduction and subsequent dissolution, sulfate reduction, and probable pyrite precipitation that are inferred from the data to occur along distinct regions of the flow-path. In general, the distribution of As species are consistent with equilibrium thermodynamics, such that arsenate dominates in more oxidizing waters near the recharge area, and arsenite predominates in the progressively reducing groundwaters beyond the recharge area.

Hydrogeochemistry of deep groundwaters in the central part of the Fennoscandian Shields

International Nuclear Information System (INIS)

Blomqvist, R.

1999-01-01

Saline groundwaters are frequent in the central part of the Fennoscandian Shield. The results indicate large variations in groundwater chemistry and in the spatial distribution of saline groundwaters. The depths of the fresh/saline groundwater boundaries vary considerably but generally the boundary is located at 300-600 m. In some cases fresh bicarbonate groundwaters are encountered throughout the drill hole. More commonly, however, bicarbonate waters occur only as an upper layer, up to a few hundred metres in extent, overlying chloride waters of varying salinity. In coastal areas saline groundwaters are frequently found much closer to ground surface. Long-term water-rock interaction and incursions of present/ancient sea water are considered the main processes affecting the evolution of the saline groundwater bodies, while isolation from the surface-close hydrological cycle seems to be a prerequisite for the preservation of these waters. Ancient preferential leaching of low-Rb/Sr minerals (most likely plagioclase) and/or fluid inclusions are the main contribution for dissolved solids in water-rock interaction. The strontium isotope results imply that saline groundwaters in crystalline rocks do not evolve as isolated small pockets with a restricted volume of rock but may constitute more open systems in which lateral hydrogeochemical interaction extends over distances of at least hundreds of metres. One potential mechanism for formation of young calcites is related to glacial rebound where release of stress and increase in temperature in fractures make the groundwaters oversaturated with respect to calcite. Δ 18 depleted groundwaters have been observed from several sampling sites in Finland, indicative of glacial meltwater intrusion in the bedrock. As saline waters have been documented to have long residence times and are not associated with active meteoric water circulation, bedrock suites hosted by saline groundwaters could be considered as potential repository

Overview of groundwater management approaches at salinisation risk

Science.gov (United States)

Polemio, Maurizio; Zuffianò, Livia Emanuela

2013-04-01

All natural waters contain dissolved minerals from interactions with atmospheric and soil gases, mixing with other solutions, and/or interactions with the biosphere and lithosphere. In many cases, these processes result in natural waters containing solute or salinity above concentrations recommended for a specified use, which creates significant social and economic problems. Groundwater salinisation can be caused by natural phenomena and anthropogenic activities. For the former case, we can distinguish terrestrial and marine phenomena. Approximately 16% of the total area of continental earth is potentially involved in groundwater salinisation. Seawater intrusion can be considered to be the primary phenomenon to be studied in terms of groundwater salinisation. Three schematic approaches to the protection of groundwater via salinisation mitigation and/or groundwater salinity improvement are described based on the classifications of the primary salinisation sources and focusing on the effect of seawater intrusion. The complexity of these approaches generally increases due to difficulties caused by groundwater quality and quantity degradation and increased demand for quality water. In order from the lowest to the highest complexity, these approaches are the engineering approach, the discharge management approach, and the water and land management approach. The engineering approach is realised on the local or detailed scale with the purpose of controlling the salinisation, optimising the well discharge with specific technical solutions and/or completing works to improve the quality and/or quantity of the discharged fresh groundwater. The discharge management approach encompasses at least an entire coastal aquifer and defines rules concerning groundwater utilisation and well discharge. The water and land management approach should be applied on the regional scale. Briefly, this approach becomes necessary when one or more need creates an overall framework of high

The effect of industrial effluent stream on the groundwater

International Nuclear Information System (INIS)

Yasar, A.; Ahmad, N.; Chaudhry, M.N.; Sarwar, M.

2005-01-01

This study was performed to investigate the effect of the industrial wastewater stream on the groundwater. Wastewater was characterized in terms of inorganic and organic constituents. Inorganic constituents included Na/sup +/, Ca/sup 2+/ K/sup +/, Cl/sup -/, NO/sub 3//sup -/ and SO/sub 4//sup 2-/ coupled with heavy metal elements such as, Cd, Cr, Pb, Mn, Cu, Ni, Fe and In. Organic load of the stream was determined in terms of chemical oxygen demand (COD), biological oxygen demand (BOD/sub 5/) and ammonia-nitrogen (NH/sub 3/-N) contents. Other characteristics were pH, electrical conductivity (EC) and total dissolved solids (TDS). The correlation coefficients between quality parameter pairs of stream water and groundwater were determined to ascertain the source of groundwater contamination. At station 1, BOD/sub 5/ and COD contents were 20 times and Cr concentration was 10 times higher than the permissible limits for stream water [1]. Contents of these parameters reflected the level of industrial and domestic pollution coming from India. However, large variations in the levels of these parameters at down stream sites of the drain were characteristic of type and nature of industrial effluents and domestic sewage joining the stream. Analysis results of more than one hundred groundwater samples from shallow and deep wells around the drain showed that groundwater of shallow aquifers was contaminated due to drain water. A comparison of the contents of these parameters in shallow wells with WHO standards showed that some parameters such as turbidity, TDS, Na/sup +/, F -and heavy metals like Cr were found higher than the permissible limits. (author)