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1.
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   

2.
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   

3.
A large number of ground water samples (360) was collected from 60 stations over six consecutive seasons to study the influence of the main sewerage drain on shallow ground water table beneath the municipal area of Cuttack, India. A majority of the samples collected from stations close to the drain exceeded the maximum permissible limits set by the World Health Organization (WHO). Almost all the samples near the drain exceeded the WHO limit for NO3- and Na+. However, the concentrations decreased as the distance from the drain increased. The winter season registered the maximum concentrations of NH4+, NO3-, and SO42- ions whereas the minimum values always coincided with the rainy season. R-mode factor analysis was conducted to find relationships amongst the 16 chemical parameters studied. Fluoride showed a negative correlation with Cl-, Na+, NO3-, SO42-, and PO43-. The concentration of F- may be lower in raw waste water than naturally occurs in the ground water. Therefore, a decrease in the concentration of F- near the drain may be attributed to dilution by contributions of waste water to the ground water. The rest of the parameters were found to be directly related to the distance of collection points to the sewerage. The distribution of nutrients is strongly affected by leaching of waste water into the ground water.  相似文献   

4.
本文利用2012年4月30日至5月10日华北地区大气湍流实验资料,分析了冬小麦田下垫面温度、湿度、二氧化碳(CO2)和甲烷(CH4)的湍流统计和输送特征,利用涡旋相关法计算的CH4通量值确定了松弛涡旋累积(REA)法计算CH4通量的经验系数.结果表明,不稳定层结下,温度、湿度、CO2和CH4的归一化标准差随稳定度参数z/L的关系满足-1/3幂次关系.热量、水汽和CO2水平方向的湍流输送和垂直方向的比值与稳定度参数z/L存在一定的相关关系,但CH4没有类似特征.实验期间,感热通量数值较低,潜热通量较高;CO2在夜间表现出微弱的向上输送,其余时段为向下输送,可以认为实验站所在地区是碳汇;CH4的湍流输送整体为向下输送,无明显的日变化规律,可以认为是CH4汇.利用松弛涡旋累积法获取CO2和CH4通量的参数取值分别为0.61和0.30.  相似文献   

5.
Abstract
Determination of chemical constituent ratios allows distinction between two salinization mechanisms responsible for shallow saline ground water and vegetative-kill areas in parts of west Texas. Mixing of deep-basin (high Cl) salt water and shallow (low Cl) ground water results in saline waters with relatively low Ca/Cl, Mg/Cl, SO44/ Cl, Br/Cl, and NO3/Cl ratios. In scattergrams of major chemical constituents vs. chloride, plots of these waters indicate trends with deep-basin brines as high Cl end members. Evaporation of ground water from a shallow water table, in contrast, results in saline water that has relatively high Ca/Cl, Mg/Cl, SO4/Cl, and Br/CL ratios. Trends indicated by plots of this water type do not coincide with trends indicated by plots of sampled brines. Leaching of soil nitrate in areas with a shallow water table accounts for high NO3 concentrations in shallow ground water.  相似文献   

6.
Hydrogen gas was discovered within the steel casing above standing water in a percussion-drilled borehole on the Hanlord Site in south-central Washington state. In situ measurements of the borehole fluids indicated anoxic, low-Eh (<-400 mV) conditions. Ground water sampled from adjacent wells in the same formation indicated that the ground water was oxygenated. H2 was generated during percussion drilling, due to the decomposition of borehole waters as a result of aqueous reactions with drilled sediment and steel from the drilling tools or casing. The generation of H2 within percussion-drilled boreholes that extend below the water table may be more common than previously realized. The ambient concentration of H2 produced during drilling was limited by microbial activity within the casing-resident fluids. H2 was generated abiotically in the laboratory, whereby sterilized borehole slurry samples produced 100 times more H2 than unsterilizcd samples. It appears that H2 is metabolized by microorganisms and concentrations might be significantly greater if not for microbial metabolism.  相似文献   

7.
Electro-osmosis (EO), the movement of water through porous media in response to an electric field, offers a means for extracting contaminated ground water from fine-grained sediments, such as clays, that are not easily amenable to conventional pump-and-treat approaches. The EO-induced water flux is proportional to the voltage gradient in a manner analogous to the flux dependence on the hydraulic gradient under Darcy's law. The proportionality constant, the soil electro-osmotic conductivity or keo, is most easily measured in soil cores using bench-top tests, where flow is one-dimensional and interfering effects attributable to Darcy's law can be directly accounted for. In contrast, quantification of EO fluxes and keo in the field under deployment conditions can be difficult because electrodes are placed in ground water wells that may be screened across a heterogeneous mixture of lithologies. As a result, EO-induced water fluxes constitute an approximate radial flow system that is superimposed upon a Darcy flow regime through permeable pathways that may or may not be coupled with hydraulic head differences created by the EO-induced water fluxes. A single well comparative tracer test, which indirectly measures EO fluxes by comparing wellbore tracer dilution rates between background and EO-induced water fluxes, may provide a means for routinely quantifying the efficacy of EO systems in such settings. EO fluxes measured in field tests through this technique at a ground water contamination site were used to estimate a mean keo value through a semianalytic line source model of the electric field. The resulting estimate agrees well with values reported in the literature and with values obtained with bench-top tests conducted on a soil core collected in the test area.  相似文献   

8.
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   

9.
Methane concentrations and selected chemical parameters in interstitial water were examined along subsurface flowpath in two subsystems (hyporheic and parafluvial sediments) in the Sitka stream, Czech Republic. Interstitial methane concentrations exhibited a distinct spatial pattern. In the hyporheic downwelling zone where the sediments are relatively well oxygenated due to high hydrologic exchange with the surface water, low interstitial methane concentrations, averaging 9.3 μg CH4/l, were found. In contrast, upwelling sediments and parafluvial sediments (active channel sediments lateral to the wetted channel) had significantly higher methane concentrations (p < 0.05, and p < 0.01, respectively), averaging 43.2 μg CH4/l and 160.5 μg CH4/l, respectively. Dissolved oxygen was the highest where surface water entered hyporheic/parafluvial sediments and decreased with water residence time in the sediments (p < 0.01). Nitrate concentrations decreased along the flowpath and were significantly lower at downstream end of the riffle (p < 0.001). Sulfate concentrations also show a slight decline with the water residence time, but differences were not significant. Effect of both nitrate and sulfate on methanogenesis is also discussed. The interstitial methane concentration significantly increased with surface water temperature (p < 0.001) and was negatively correlated with redox potential (p < 0.01) and dissolved oxygen (p < 0.05).  相似文献   

10.
A direct aqueous injection capillary gas chromatography/flame ionization (GC/FID) procedure for the analysis of petroleum-contaminated water was developed and applied to seven water samples saturated with different petroleum products. Separation of C1 to C4 alcohols, C6 to C9 monoaromatics, MTBE, phenol, aniline, and other compounds, and the detection of BTEX compounds at concentrations at or below their maximum contaminant levels (MCLs) is reported. Among the test compounds analyzed, the only pair found to coelute were 1-butanol and benzene. A method for confirmation of alcohols and polar compounds in the presence of dissolved petroleum hydrocarbons was also evaluated. In this case, water samples were analyzed before and after purging. Polar compounds were found to be significant components of the water soluble fractions of commercial petroleum products.  相似文献   

11.
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   

12.
The area surrounding the Colorado Department of Transportation Materials Testing Laboratory in Denver was the subject of intense investigation, involving the collection of thousands of ground water, soil-gas, and indoor air samples in order to investigate indoor air impacts associated with a subsurface release of chlorinated solvents. The preremediation portion of that data set is analyzed and reduced in this work to ground water–to-indoor air attenuation factors (αgw= the ratio of the measured indoor air concentration to the soil-gas concentration predicted to be in equilibrium with the local ground water concentration). The empirical αgw values for this site range from about 10−6 to 10−4 with an overall average of 3 × 10−5 (μg/L indoor air)/(μg/L soil gas). The analysis of this data set highlights the need for a thorough data review and data screening when using large data sets to derive empirical relationships between subsurface concentrations and indoor air. More specifically, it is necessary to identify those parts of the data that contain a strong vapor intrusion pathway signal, which generally will require concentrations well above reported detection levels combined with spatial or temporal correlation of subsurface and indoor concentrations.  相似文献   

13.
We investigated the distribution of naturally occurring geochemical tracers (222Rn, 223Ra, 224Ra, 226Ra, CH4, δ18O, and δ2H) in the water column and adjacent groundwater of Mangueira Lagoon as proxies of groundwater discharge. Mangueira Lagoon is a large (90 km long), shallow (4–5 m deep), fresh, and non-tidal coastal lagoon in southern Brazil surrounded by extensively irrigated rice plantations and numerous irrigation canals. We hypothesized that the annual, intense irrigation for rice agriculture creates extreme conditions that seasonally change groundwater discharge patterns in the adjacent lagoon. We further supposed that dredging of irrigation canals alters groundwater fluxes.

While the activities of 222Rn in shallow groundwater were 2–3 orders of magnitude higher than in surface water, CH4 and radium isotopes were only 1 order of magnitude higher. Therefore, 222Rn appears to be the preferred groundwater tracer in this system. Radon concentrations and conductivities were dramatically higher near the pump house of rice irrigation canals, consistent with a groundwater source. Modeling of radon inventories accounting for total inputs (groundwater advection, diffusion from sediments, and decay of 226Ra) and losses (atmospheric evasion, horizontal mixing and decay) indicated that groundwater advection rates in the irrigation canals (25 cm/d) are over 2 orders of magnitude higher than along the shoreline (0.1 cm/d). Nearly 75% of the total area of the canals is found in the southern half of the lagoon, where groundwater inputs seem to be higher as also indicated by methane and stable isotope trends. In spite of the relatively small area of the canals, we estimate that they contribute nearly 70% of the total (57,000 m3/d) groundwater input into the entire Mangueira Lagoon. We suggest that the dredging of these canals cut through aquitards which previously restricted upward advection from the underlying permeable strata. The irrigation channels may therefore represent an important but previously overlooked source of nutrients and other dissolved chemicals derived from agricultural practices into the lagoon.  相似文献   


14.
Azimuth-dependent AVO in reservoirs containing non-orthogonal fracture sets   总被引：1，自引：0，他引：1  
Azimuthal anisotropy in rocks can result from the presence of one or more sets of partially aligned fractures with orientations determined by the stress history of the rock. The symmetry of a rock with horizontal bedding that contains two or more non-orthogonal sets of vertical fractures may be approximated as monoclinic with a horizontal plane of mirror symmetry. For offsets that are small compared with the depth of the reflector, the azimuthal variation in P-wave AVO gradient for such a medium varies with azimuth as     where φ is the azimuth measured with respect to the fast polarization direction for a vertically polarized shear wave. φ 2 depends on both the normal compliance B N and the shear compliance B T of the fractures and may differ from zero if B N B T varies significantly between fracture sets. If B N B T is the same for all fractures,     and the principal axes of the azimuthal variation in P-wave AVO for fixed offset are determined by the polarization directions of a vertically propagating shear wave. At larger offsets, terms in     and     are required to describe the azimuthal variation in AVO accurately. φ 4 and φ 6 also depend on B N B T. For gas-filled open fractures     but a lower value of B N B T may result from the presence of a fluid with non-zero bulk modulus.  相似文献   

15.
Electromigration is proposed as an in situ method for preconcentrating contaminants in ground water prior to pumping and treating. In earlier investigations by the senior author and co-workers, it was found that Cu in synthetic ground water migrated strongly to a Pt cathode and plated out as metallic copper. In the present study, carbon electrodes were inserted into a laboratory column of fine quartz sand that was saturated with a lower concentration of CuSO4 solution. A fixed potential of 2.5 V was applied, causing dissolved Cu and SO4 to accumulate strongly at the cathode and anode, respectively. Only minor plating-out of Cu took place on the carbon electrodes. In addition to the use of carbon electrodes, the present research also investigated the effects of a lower concentration of metal, accumulation of SO4 adjacent to the anodes, adsorption of Cu on the sand, and competition by moving ground water.
At an imposed voltage of 2.5 V and in the presence of 65 mg/L of dissolved Cu and 96 mg/L of SO4 (0.001 M CuSO4 solution), electrolysis of water caused large changes in the pH and speciation of the aqueous components, as well as precipitation of solid Cu-hydroxides. Significant retardation of Cu occurred in the presence of ground water flowing at an average intergranular velocity of 0.2 m/day, but only minor retardation at water velocities of 1.9 and 2.9 m/day.
Sulfate tends to migrate strongly to the anodes, suggesting that in situ electromigration may offer a useful new method for preconcentrating such highly soluble ions as SO4, NO3, and CI that are difficult to remove by conventional pump-and-treat methods. A number of potential problems exist that should be addressed in a field test.  相似文献   

16.
A small stream in the Great Plains of USA was sampled to understand the streamflow components following intense precipitation and the influence of water storage structures in the drainage basin. Precipitation, stream, ponds, ground-water and soil moisture were sampled for determination of isotopic (D, 18O) and chemical (Cl, SO4) composition before and after two intense rain events. Following the first storm event, flow at the downstream locations was generated primarily through shallow subsurface flow and runoff whereas in the headwaters region – where a pond is located in the stream channel – shallow ground-water and pond outflow contributed to the flow. The distinct isotopic signatures of precipitation and the evaporated pond water allowed separation of the event water from the other sources that contributed to the flow. Similarly, variations in the Cl and SO4 concentrations helped identify the relative contributions of ground-water and soil moisture to the streamflow. The relationship between deuterium excess and Cl or SO4 content reveals that the early contributions from a rain event to streamflow depend upon the antecedent climatic conditions and the position along the stream channel within the watershed. The design of this study, in which data from several locations within a watershed were collected, shows that in small streams changes in relative contributions from ground water and soil moisture complicate hydrograph separation, with surface-water bodies providing additional complexity. It also demonstrates the usefulness of combined chemical and isotopic methods in hydrologic investigations, especially the utility of the deuterium excess parameter in quantifying the relative contributions of various source components to the stream flow.  相似文献   

17.
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   

18.
对首都圈地区跨18条活动断裂的35条剖面进行了土壤气浓度和通量测量, 结果显示: 各测量剖面土壤气Rn, Hg和CO2的浓度平均值分别为3.2—45.0 kBq/m3, 3.9—24.9 ng/m3和0.154%—2.175%; 其通量平均值分别为3.8—152.1 mBq/(m2·s), 0.1-42.6 ng/(m2·h)和8.5—89.4 g/(m2·d)． 研究区土壤气Rn, Hg和CO2的浓度和通量均呈东高西低的变化趋势, 与首都圈地区由西至东应力水平增高、 地壳厚度逐渐减薄、 沉积层厚度增大、 地震活动逐渐增强等趋势相对应, 这表明首都圈地区土壤气的区域地球化学特征主要受控于上地壳物质结构、 深部气体补给和地震活动, 同时也受到自然环境及土壤类型的影响．   相似文献   

19.
Seismic velocities ( V p and V s) of compressional (P-) and shear (S-) waves are important parameters for the characterization of marine sediments with respect to their sedimentological and geotechnical properties. P- and S-wave velocity data of near-surface marine sediments (upper 9 m) of the continental slope of the Barents Sea are analysed and correlated to sedimentological and geotechnical properties. The results show that the S-wave velocity is much more sensitive to changes in lithology and mechanical properties than the P-wave velocity, which is characterized by a narrow range of values. The correlation coefficients between S-wave velocity and silt and clay content, wet bulk density, porosity, water content and shear strength are higher than 0.5 while the correlation coefficients of P-wave velocity and the same parameters are always lower than 0.4. Although the relationship between V s and clay content has been widely described, the data show that V s is better correlated with silt content than with clay content for the sediments of the area investigated. However, they show different trends. While V s increases with increasing clay content, it decreases with increasing silt content.  相似文献   

20.
Large differences in chemistry between sampling points separated In short vertical intervals are often observed in contaminant plumes in both granular and fractured aquifers. However, most regional models assume that such differences will be reduced by dispersive mixing during transport. At a field site located in a discharge area on the Oak Ridge Reservation, Tennessee, ground water flows along discrete flowpaths, as evidenced by the presence of four distinct water types—Ca-HCO3, Ca-Na-HCO3, and Na-Ca-HCO3, and Na-Ca-HCO3-S04—in samples collected from shallow (< 3D in) multilevel wells. The preservation of distinct chemical signatures suggests that ground water must he contained in discrete flow zones during much of its transport time. The chemical composition of the water types can be explained primarily by strata-bound flow over varying flowpath lengths and secondarily by mixing of waters during cross-formational flow in a discharge zone. The hydrochemical facies identified by correlation of water types between the boreholes indicate the general orientation of ground water How paths. These inferred flowpaths are oblique to the orientation of the measured hydraulic gradient and are more closely aligned with bedding and the calculated flow direction. Results of this study indicate that discrete multilevel sampling for analysis of major ions, in addition to information gathered from tracer tests, borehole flow tests. and visual core observations, can provide valuable information on flow directions and preferential flowpaths for contaminant transport.  相似文献   

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