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1.
Sharma S  Frost CD 《Ground water》2008,46(2):329-334
Recovery of hydrocarbons commonly is associated with coproduction of water. This water may be put to beneficial use or may be reinjected into subsurface aquifers. In either case, it would be helpful to establish a fingerprint for that coproduced water so that it may be tracked following discharge on the surface or reintroduction to geologic reservoirs. This study explores the potential of using δ13C of dissolved inorganic carbon (DIC) of coalbed natural gas (CBNG)–coproduced water as a fingerprint of its origin and to trace its fate once it is disposed on the surface. Our initial results for water samples coproduced with CBNG from the Powder River Basin show that this water has strongly positive δ13CDIC (12‰ to 22‰) that is readily distinguished from the negative δ13C of most surface and ground water (−8‰ to −11‰). Furthermore, the DIC concentrations in coproduced water samples are also high (more than 100 mg C/L) compared to the 20 to 50 mg C/L in ambient surface and ground water of the region. The distinctively high δ13C and DIC concentrations allow us to identify surface and ground water that have incorporated CBNG-coproduced water. Accordingly, we suggest that the δ13CDIC and DIC concentrations of water can be used for long-term monitoring of infiltration of CBNG-coproduced water into ground water and streams. Our results also show that the δ13CDIC of CBNG-coproduced water from two different coal zones are distinct leading to the possibility of using δ13CDIC to distinguish water produced from different coal zones.  相似文献   

2.
Pore water collected from piezometers installed in a thick clay-rich till were used to compare and evaluate four techniques for obtaining δD and δ18O values in these media. The techniques included mechanical squeezing, centrifugation, azeotropic distillation, and a direct soil-water equilibration technique. Direct CO2-core equilibration yielded sufficiently accurate and reproducible δ18O results of pore water in clay-rich tills. In addition, this method eliminated the need for labor-intensive complete extraction of water from the geologic media. Mechanical squeezing and centrifugation produced results similar to direct equilibration. However, both of these methods exhibited a greater degree of variability and were laborious and more time consuming. Small differences in δ18O values between piezometer water and equilibrated, squeezed, and centhfuged samples suggested that each method collected different fractions of the clay-water reservoir. Although these subtle differences were not conclusive, they did suggest the presence of weakly bound water and highlighted the difference between these three techniques for determining the stable isotopic composition of pore water in clay-rich aquitards. Azeotropic distillation produced a high level of discrepancy in δD andδ18O results compared to the other methods. Incomplete extraction was considered the most probable cause of this error. The results of this study suggested that direct equilibration is the best method for determining detailed δD and δ18O values of pore water in clay-rich aquitards.  相似文献   

3.
Non-point source pollution of ground water systems has become a national concern in recent years. Researchers and regulatory agencies are investigating the source and processes of the contamination. Agricultural best management practices (BMPs) traditionally developed to reduce non-point source pollution of surface water resources are being investigated for their impact on ground water quality. This study used the CREAMS model to simulate the long-term effects of seven different BMPs on nitrate nitrogen (NO3-N) loadings to a shallow, unconfined ground water system. Two representative watersheds, 5.8 and 8.9 hectares (14.3 and 22 acres) in area, in the Coastal Plain physiographic region of Maryland were selected for study. Soils in these watersheds belong to the Matapeake silt loam series and have moderate infiltration capacity. Results from this study indicated that BMPs used in conjunction with winter cover (barley) reduced NO3-N leaching to the ground water system. It was also found that turfgrass reduced surface losses of water and nitrogen, but increased leaching losses of water and NO3-N significantly. All of the BMPs simulated in this study resulted in leachate NO3-N concentrations exceeding 10 ppm, the U.S. EPA health standard for public drinking water, indicating a need for alternate practices for reducing nitrate leaching.  相似文献   

4.
Soil-solution samplers and shallow ground water monitoring wells were utilized to monitor nitrate movement to ground water following H2O2 application to a clogged soil absorption system. Nitrate-nitrogen concentrations in soil water and shallow ground water ranged from 29 to 67 mg/L and 9 to 22 mg/L, respectively, prior to H2O2 treatment. Mean nitrate-nitrogen concentrations in soil water and ground water increased and ranged from 67 to 115 mg/L and 23 to 37 mg/L, respectively, one week after H2O2 application. Elevated concentrations of nitrate-nitrogen above background persisted for several weeks following H2O2 treatment. The H2O2 treatment was unsuccessful in restoring the infiltrative capacity of a well-structured soil. Application of H2O2 to the soil absorption system poses a threat of nitrate contamination of ground water and its usefulness should be fully evaluated before rehabilitation is attempted.  相似文献   

5.
Machida I  Lee SH 《Ground water》2008,46(4):532-537
We observed long-term changes in the concentrations of dissolved ions in ground water caused by leachate from new volcanic ejecta deposited on the ground surface of the volcanic Miyakejima Island, Japan. Water samples were collected from nine wells and two rain collectors over a period of more than 10 years, and samples of runoff water were collected periodically. The samples were analyzed for temperature, pH, alkalinity, Cl−, and SO42−; some of the samples were also analyzed for δ13C. Because the leachate from the volcanic ejecta contained sulfate, we recorded an increase in SO42− concentrations in the (unconfined) well water. The increase in SO42− was initially detected between less than 1.4 and 5.2 years after the eruption, showing peak concentrations from 2.4 to 6.4 years after the eruption. This delayed response reflects the transit time of downward-moving SO42− in the vadose zone, corresponding to an apparent movement rate of 0.4 to 7.2 cm/d. The rate relates to the mean recharge, represented as a fraction of local mean rainfall, and is calculated using the Cl− balance method. The magnitude of the recorded increases reflects the volume of volcanic mudflow on the ground surface within the basin. For the management of ground water after an eruption, it is therefore important to know the chemical properties of the volcanic ejecta and the spatial distribution of mudflow to estimate the magnitude of the effect of ejecta on ground water quality.  相似文献   

6.
To assess the vulnerability of ground water to contamination in the karstic Upper Floridan aquifer (UFA), age-dating tracers and selected anthropogenic and naturally occurring compounds were analyzed in multiple water samples from a public supply well (PSW) near Tampa, Florida. Samples also were collected from 28 monitoring wells in the UFA and the overlying surficial aquifer system (SAS) and intermediate confining unit located within the contributing recharge area to the PSW. Age tracer and geochemical data from the earlier stage of the study (2003 through 2005) were combined with new data (2006) on concentrations of sulfur hexafluoride (SF6), tritium (3H), and helium-3, which were consistent with binary mixtures of water for the PSW dominated by young water (less than 7 years). Water samples from the SAS also indicated mostly young water (less than 7 years); however, most water samples from monitoring wells in the UFA had lower SF6 and 3H concentrations than the PSW and SAS, indicating mixtures containing high proportions of older water (more than 60 years). Vulnerability of the PSW to contamination was indicated by predominantly young water and elevated nitrate-N and volatile organic compound concentrations that were similar to those in the SAS. Elevated arsenic (As) concentrations (3 to 19 μg/L) and higher As(V)/As(III) ratios in the PSW than in water from UFA monitoring wells indicate that oxic water from the SAS likely mobilizes As from pyrite in the UFA matrix. Young water found in the PSW also was present in UFA monitoring wells that tap a highly transmissive zone (43- to 53-m depth) in the UFA.  相似文献   

7.
Vertical depth profiles of pore water isotopes (δD and δ18O) in clay-rich aquitards have been used to show that solute transport is dominated by molecular diffusion, to define the timing of geologic events, and to estimate vertical hydraulic conductivity. The interpretation of the isotopic profiles in these studies was based on pore water samples collected from piezometers installed in nests (typically 4 to 15 piezometers) over depths of 10 to 80 m. Data from piezometer nests generally have poor vertical resolution (meters), raising questions about their capacity to reveal the impact of finer scale heterogeneities such as permeable sand bodies or fractured till zones on solute transport. Here, we used high-resolution (30-cm) depth profiles of δD and δ18O from two continuously cored boreholes in a till aquitard to provide new insights into the effects of sand bodies on solute transport. High-resolution core-derived profiles indicate that such heterogeneities can cause major deviations from one-dimensional diffusion profiles. Further, comparison of piezometer-measured values with best-fit diffusion trends shows subtle deviations, suggesting the presence of heterogeneities that should not be ignored. High-resolution profiles also more clearly defined the contact between the highly fractured oxidized zone and the underlying unoxidized zone than the piezometers.  相似文献   

8.
Methyl tert -butyl ether (MTBE) and benzene have been measured since 1993 in a shallow, sandy aquifer contaminated by a mid-1980s release of gasoline containing fuel oxygenates. In wells downgradient of the release area, MTBK was detected before benzene, reflecting a chromatographic-like separation of these compounds in the direction of ground water flow. Higher concentrations of MTBE and benzene were measured in the deeper sampling ports of multilevel sampling wells located near the release area, and also up to 10 feet (3 m) below the water table surface in nested wells located farther from the release area. This distribution of higher concentrations at depth is caused by recharge events that deflect originally horizontal ground water flowlines. In the laboratory, microcosms containing aquifer material incubated with uniformly labeled 14C-MTBE under aerobic and anaerobic. Fe(III)-reducing conditions indicated a low but measurable biodegradation potential (<3%14C-MTBW as 14CO2) after a seven-month incubation period, Tert -butyl alcohol (TBA), a proposed microbial-MTBE transformation intermediate, was detected in MTBE-contaminated wells, but TBA was also measured in unsaturated release area sediments. This suggests that TBA may have been present in the original fuel spilled and does not necessarily reflect microbial degradation of MTBE. Combined, these data suggest that milligram per liter to microgram per liter decreases in MTBE concentrations relative to benzene are caused by the natural attenuation processes of dilution and dispersion with less-contaminated ground water in the direction of flow rather than biodegradation at this point source gasoline release site.  相似文献   

9.
Masaaki  Okuda  Hiroomi  Nakazato  Norio  Miyoshi  Takeshi  Nakagawa  Hiroko  Okazaki  Saneatsu  Saito  Asahiko  Taira 《Island Arc》2006,15(3):338-354
Abstract   The 250-m Choshi core (CHOSHI-1), drilled from hemipelagic muds of the Inubo Group, has been physically, geochemically and tephrochronologically analyzed back to 1 Ma. We provide pollen results for the 19–169 m section of the core (400–780 ka) bracketed by the marker tephra Ty1 (equivalent to J4) and the Brunhes–Matuyama paleomagnetic boundary. The results show good agreement with the corresponding oxygen isotope (δ18O) profile, with high δ18O intervals dominated by boreal conifers Picea , Abies , Pinus (subgen. Haploxylon ) and Tsuga ( diversifolia ), whereas low δ18O intervals are dominated by temperate conifers Cryptomeria , Taxaceae-Cephalotaxaceae-Cupressaceae and Sciadopitys . In order to confirm pollen-climate relations for the relevant taxa, a modern surface pollen dataset for the Japanese archipelago was consulted. In this analysis, the ratios of Cryptomeria / Picea and temperate/boreal conifers serve as proxies for the 100-kyr glacial/interglacial cycle during the Middle Pleistocene. Distinct signals for marine isotope stages (MIS) 11, 12, 13–15, 16, 17 and 18–19 are recognized in accordance with the tephrochronology and δ18O of the same core. Application of the criteria to an independent pollen record from Lake Biwa provides an integrated pollen stratigraphy for mid-latitude Japan during the past 800 ky. Some degree of uncertainty remains in the chronology of the MIS13–15 interval, relating to the uncertainty in the eruption age of widespread tephra Ks11.  相似文献   

10.
A six year field experiment has shown that a sand-bentonite mixture used to seal monitoring wells in aquitards contributes solutes to the ground water sampled from these wells. Monitoring wells were installed at field sites with hydraulic conductivity (K) ranging from 5 × 10 -9 m/s to 3 × 1011 m/s. In most cases the boreholes remained dry during installation which allowed the placement of a dry powdered bentonite/sand mixture tagged with potassium bromide (KBr) to seal and separate sampling points. Over six years, wells were sampled periodically and ground-water samples were analyzed for Br and Cl and other major ions. Typical Br results ranged from 10 mg/1 to 35 mg/1 in the first 700 days, as compared to an estimated initial concentration in the seal material of about 75 mg/1. After six years the bromide concentrations had decreased to between 3 mg/1 and 5 mg/1. The total mass of Br removed in six years is less than 50% of that placed; therefore the contamination effects, although considerably diminished, persist. The trends of Br, Cl, Na, and SO4 indicate that varying degrees of contamination occur. These data show that the materials used to seal monitoring wells in aquitards can have a significant and long-lasting impact on the chemistry of the water in the wells.  相似文献   

11.
Tomohiro  Toki  Toshitaka  Gamo  Urumu  Tsunogai 《Island Arc》2006,15(3):285-291
Abstract   We collected free-gas and in situ fluid samples up to a depth of 200.6 m from the Sagara oil field, central Japan (34°44'N, 138°15'E), during the Sagara Drilling Program (SDP) and measured the concentrations and stable carbon isotopic compositions of CH4 and C2H6 in the samples. A combination of the CH4/C2H6 ratios with the carbon isotope ratios of methane indicates that the hydrocarbon gases are predominantly of thermogenic origin at all depths. The isotope signature of hydrocarbon gases of δ13      < δ13     suggests that these gases in the Sagara oil field are not generated by polymerization, but by the decomposition of organic materials.  相似文献   

12.
The artificial sweetener acesulfame (ACE) is a potentially useful tracer of waste water contamination in groundwater. In this study, ACE concentrations were measured in waste water and impacted groundwater at 12 septic system sites in Ontario, Canada. All samples of septic tank effluent (n = 37) had ACE >6 µg/L, all samples of groundwater from the proximal plume zones (n = 93) had ACE >1 µg/L and, almost all samples from the distal plume zones had ACE >2 µg/L. Mean mass ratios of total inorganic nitrogen/ACE at the 12 sites ranged from 680 to 3500 for the tank and proximal plume samples. At five sites, decreasing ratio values in the distal zones indicated nitrogen attenuation. These ratios were applied to three aquifers in Canada that are nitrate‐stressed and an urban stream where septic systems are present nearby to estimate the amount of waste water nitrate contamination. At the three aquifer locations that are agricultural, low ACE values (<0.02‐0.15 µg/L) indicated that waste water contributed <15% of the nitrate in most samples. In groundwater discharging to the urban stream, much higher ACE values (0.2‐11 µg/L) indicated that waste water was the likely source of >50% of the nitrate in most samples. This study confirms that ACE is a powerful tracer and demonstrates its use as a diagnostic tool for establishing whether waste water is a significant contributor to groundwater contamination or not.  相似文献   

13.
Hui-Long  Xu  Jian-Wei  Shen Xue-Wu  Zhou 《Island Arc》2006,15(1):199-209
Abstract   Geothermal waters in the Niigata Sedimentary Basin, central Japan, are divided into four groups based on their chemical composition (i.e. Na-SO4-type, Na-SO4-Cl-type, Na-Cl-type and Na-Cl-HCO3-type). The Na-SO4-type geothermal water forms as a consequence of water–rock interaction and generally occurs in the outer part of the basin. The Na-Cl-type geothermal water is further subdivided into the original Na-Cl-type geopressured thermal water and the mixed Na-Cl-type geothermal water, in terms of its geochemical and isotopic composition. The original Na-Cl-type geopressured thermal water originates from a geopressured hydrothermal system containing the altered fossil formation waters that are sealed at depth. It moves up to the upper part of the depositional succession or the ground, and generally does not mix with groundwater that is of meteoric origin. This type of water is cooled by heat conduction. The concentration of Cl– in this type of thermal water is very similar to that in seawater. The δD and δ18O values are approximately constant and independent of temperature. The original Na-Cl-type geopressured thermal water is distributed mainly along anticlinal axes in folded Neogene formations. The mixed Na-Cl-type geothermal water is related to the expulsion activity of the geopressured hydrothermal system and occurs mostly along active faults. It is formed by shallow groundwater of meteoric origin being mixed with geopressured hydrothermal water when the geopressured hydrothermal system was expulsed along active faults by paroxysmal tectonic events.  相似文献   

14.
Using nitrate to quantify quick flow in a karst aquifer   总被引：3，自引：0，他引：3  
Mahler BJ  Garner BD 《Ground water》2009,47(3):350-360
In karst aquifers, contaminated recharge can degrade spring water quality, but quantifying the rapid recharge (quick flow) component of spring flow is challenging because of its temporal variability. Here, we investigate the use of nitrate in a two-endmember mixing model to quantify quick flow in Barton Springs, Austin, Texas. Historical nitrate data from recharging creeks and Barton Springs were evaluated to determine a representative nitrate concentration for the aquifer water endmember (1.5 mg/L) and the quick flow endmember (0.17 mg/L for nonstormflow conditions and 0.25 mg/L for stormflow conditions). Under nonstormflow conditions for 1990 to 2005, model results indicated that quick flow contributed from 0% to 55% of spring flow. The nitrate-based two-endmember model was applied to the response of Barton Springs to a storm and results compared to those produced using the same model with δ18O and specific conductance (SC) as tracers. Additionally, the mixing model was modified to allow endmember quick flow values to vary over time. Of the three tracers, nitrate appears to be the most advantageous because it is conservative and because the difference between the concentrations in the two endmembers is large relative to their variance. The δ18O-based model was very sensitive to variability within the quick flow endmember, and SC was not conservative over the timescale of the storm response. We conclude that a nitrate-based two-endmember mixing model might provide a useful approach for quantifying the temporally variable quick flow component of spring flow in some karst systems.  相似文献   

15.
Beginning in 1990, 2,588 wells were sampled within the Inner Coastal Plain of Georgia in an effort to assess the quality of ground water in this major farm belt. The project was one aspect of an EPA-sponsored program to assess ground-water quality statewide. Several variables were measured, including pH, specific conductivity, dissolved oxygen, temperature, nitrate, nitrite, total hardness, calcium, magnesium, and bicarbonate. In some wells sulfate, chloride, potassium, iron, and manganese contents were also determined. Particular emphasis was placed, however, on pH, specific conductivity, temperature, and nitrite/nitrate content. Generally, pH was between 6 and 8, and temperatures were within a range of 18° and 24°Celsius. Measurements of specific conductivity varied, but averaged 250–275 microsiemens/cm. Nitrite contamination was negligible, and nitrate contamination of the ground water within the shallow aquifers did not appear to be significant. In fact, 56% of the wells sampled showed no detectable signs of nitrate or nitrite contamination. There were, however, a few isolated wells where nitrate as nitrogen measurements exceeded the EPA's Safe Drinking Water Standard of 10 ppm. The general lack of contamination may be the result of the nature of the agricultural practices used in this region and/or the effect of natural denitrification.  相似文献   

16.
Akira  Imai  Nobuo  Geshi  Taketo  Shimano  Setsuya  Nakada 《Island Arc》2007,16(1):83-92
Abstract   The variation of sulphur isotopic composition during the 2000 eruption of the Miyakejima Volcano was examined in order to monitor the temporal change of the volcanic activity. The δ34S values of water-soluble sulphate leached from volcanic ash effused during intermittent eruptions from July to September 2005 range from +5 to +11‰ with a fluctuation of ca 3‰ within a single eruption. The δ34S value of sulphuric acid mist collected with 'Cu-metal trap' placed on the flank of the volcano from December 2000 to January 2001 is +6.2‰. These sulphur isotopic compositions of sulphate, which were isotopically equilibrated in the subvolcanic hydrothermal system, indicate that the temperature of the hydrothermal system beneath the caldera increased after the period of intermittent phreatic and phreatomagmatic eruptions. Then, the δ34S value of sulphuric acid trapped from January to March 2001 was +9.0‰ and the δ34S value of water-soluble sulphate on volcanic ash emitted with minor eruption in May 2001 was +11.0‰, suggesting a decrease in temperature of the subvolcanic hydrothermal system.  相似文献   

17.
Abstract Isotopic compositions of He, Ne and Ar were measured on Plio–Quaternary alkaline basalts of Marib–Sirwah and Shuqra volcanic fields in Yemen, south-western Arabian Peninsula. Very high 3He/4He isotope ratios were found in olivine phenocrysts of some Quaternary alkaline basalts in both volcanic fields, located on the margin of the dispersed Afar mantle plume, compared with the Afar–Ethiopian province in the center of the mantle plume. This suggests that the Afar mantle plume source may consist of common component (C or focal zone (FOZO)) with variable primordial 3He/4He ratio rather than high μ mantle (HIMU) component. The three component mixing C as the Afar mantle plume, depleted mantle (DM) as upper mantle and lithospheric mantle with a hybrid enriched mantle I–II (EM I–EM II) characteristics may be adequate to explain He–Sr–Nd–Pb isotope variation for the Afar–Arabian Cenozoic volcanics. The occurrence of high 3He/4He ratios in the Marib–Sirwah volcanic field appears to show that the primitive basaltic magma, derived from the margin of the dispersed trous-like Afar mantle plume during 15–0 Ma, was not by contamination of lithospheric and upper mantle materials in comparison with that from the center of the Afar mantle plume as a result of relatively low thermal anomaly.  相似文献   

18.
Benzene, toluene, ethylbenzene, and xylene (BTEX) hydrocarbons are typically the most abundant carbon source for bacteria in gasoline-contaminated ground water. In situ bioremediation strategies often involve stimulating bacterial heterotrophic production in an attempt to increase carbon demand of the assemblage. This may, in turn, stimulate biodegradation of contaminant hydrocarbons. In this study, ground water circulation wells (GCWs) were used as an in situ treatment for a fuel-contaminated aquifer to stimulate bacterial production, purportedly by increasing oxygen transfer to the subsurface, circulating limiting nutrients, enhancing bioavailability of hydrocarbons, or by removing metabolically inhibitory volatile organics. Bacterial production, as measured by rates of bacterial protein synthesis, was stimulated across the zone of influence (ZOI) of a series of GCWs. Productivity increased from ∼102 to >105 ng C/L hour across the ZOI, suggesting that treatment stimulated overall biodegradation of carbon sources present in the ground water. However, even if BTEX carbon met all bacterial carbon demand, biodegradation would account for <4.3% of the total estimated BTEX removed from the ground water. Although bacterial productivity measurements alone cannot prove the effectiveness of in situ bioremediation, they can estimate the maximum amount of contaminant that may be biodegraded by a treatment system.  相似文献   

19.
Shunso  Ishihara Akira  Sasaki 《Island Arc》1994,3(2):122-130
Abstract Sulfide minerals of late Cenozoic vein-type deposits of southwest Hokkaido and Kuril Islands yielded δ34CDT S values of 2 to 8 permil, which are typical green-tuff values of magnetite-series igneous terrane. Sulfides of the Kitami district of northeast Hokkaido, on the other hand, are characterized by negative δ34SCDT values, ranging from 0 to - 7 permil. This unique value among ore deposits in the late Cenozoic back-arc terranes in the Japanese Islands is considered to have resulted from extraction of 32S enriched sulfur from the basement rocks, because of well-developed N-S fracturing in the basement, which is characteristic of the axial belt and Kitami district of Hokkaido.  相似文献   

20.
Nitrate concentrations in ground water on Long Island, New York, have increased markedly in the last 30 years. A significant amount of this increase has been attributed to lawn and garden fertilizers in addition to cesspool and septic-tank discharges. The increase in nitrate concentration is of particular concern in the central and eastern part of the island, where ground water is the sole source of drinking water. Ground-water samples were collected from 14 wells screened near the water table in the sewered Twelve Pines housing development constructed in Medford, Suffolk County, in 1970. Samples were collected during 1972–79 and analyzed for total ammonium, organic nitrogen, and nitrate. Statistical analyses indicate that concentrations of nitrate-nitrogen in water from 10 of the wells increased significantly during 1972–79; those in water from the other four wells did not. Nitrogen loads were estimated to be 2,300 kg/yr from fertilizers, less than 80 kg/yr from irrigation water, 200 kg/yr from animals, and less than 670 kg/yr from precipitation. Leakage from sewers was considered negligible. Nitrate-nitrogen isotope ratios also suggest that the greatest source of nitrogen is from cultivation sources (either mineralized soil nitrogen or fertilizers) rather than human or animal wastes.  相似文献   

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