The Correlation Between Bedrock Uranium and Dissolved Radon in Ground Water of a Fractured Carbonate Aquifer in Southwestern Ohio

Two hypotheses have previously been proposed for the source of elevated radon in ground water of southwestern Ohio: (1) penecontemporaneous uranium at the Silurian-Ordovician unconformity, and/or (2) parent radionuclides transported from fragments of uranium-rich Ohio Shale within the glacial drift above the aquifer. To further test the first hypothesis, vertical profiles of dissolved radon in ground water and uranium in rock cores were obtained at two locations immediately underlain by the Silurian/Ordovician unconformity. Radon concentrations exceeding 1000 pCi/l occurred in zones where the bedrock had uranium concentrations greater than 1.5 ppm. Radon concentrations of less than 500 pCi/l occurred in zones where the rock had uranium concentrations below 0.25 ppm. A log-linear regression model between uranium and radon had a correlation coefficient of 0.82. Three aspects of the results support the hypothesis that the source is transported, although not necessarily from fragments of Ohio Shale. First, the high uranium-radon zones did not occur consistently or exclusively at the Silurian/Ordovician unconformity. Second, the high uranium-radon zones are correlated to fracture zones having a higher hydraulic conductivity and thus appear to be related to the zones of greater flow and transport. Third, the amount of uranium-radon disequilibrium increases exponentially with increasing hydraulic conductivity. The hypothesis of a penecontemporaneous source, not supported by our study, arose when previous investigators conducted regional surveys of domestic wells and springs and found a correspondence between elevated radon and the location of the Silurian-Ordovician unconformity. The observations of the previous investigators can be explained by the fact that the basal Silurian is in some places a horizon of higher hydraulic conductivity that facilitates transport. The two most probable external sources of uranium would be uranium-containing detritus in the glacial drift or uranium-containing phosphate fertilizers spread on the surface. Given that the uranium was transported into the aquifer during the Holocene, it could not have generated enough radium in the time elapsed since entering the aquifer to produce the radon levels that were measured. This observation indicates that radium was cotransported with uranium into the zones of high radon.     

Radon-222 in groundwater of the Long Valley caldera,California

In the Long Valley caldera, where seismicity has continued essentially uninterrupted since mid-1980 and uplift is documented, samples of water from hot, warm, and cold springs have been collected since September, 1982, and their²²²Rn concentrations analyzed. Concurrently, rocks encompassing the hydrologic systems feeding the springs were analyzed for their radioelement contents, because their uranium is the ultimate source of the²²²Rn in the water.The²²²Rn concentration in the springs varies inversely with their temperature and specific conductance. High concentrations (1500 to 2500 picocuries per liter) occur in dilute cold springs on the margins of the caldera, while low contents (12 to 25 pCi/l) occur in hot to boiling springs. Springwater radon concentrations also correlate slightly with the uranium content of the encompassing rocks.A continuous monitoring system was installed in August, 1983, at a spring issuing from basalt, to provide hourly records of radon concentration. A gamma detector is submerged in a natural pool, and we have observed that the radioactivity measured in this manner is due almost entirely to the²²²Rn concentration of the water. Initial operation shows diurnal and semidiurnal variations in the²²²Rn concentration of the springwater that are ascribed to earth tides, suggesting that those variations are responding to small changes in stress in the rocks encompassing the hydrologic system.     

Static and push-pull methods using radon-222 to characterize dense nonaqueous phase liquid saturations

Naturally occurring radon in ground water can potentially be used as an in situ partitioning tracer to characterize dense nonaqueous phase liquid (DNAPL) saturations. The static method involves comparing radon concentrations in water samples from DNAPL-contaminated and noncontaminated portions of an aquifer, while the push-pull method involves the injection (push) and extraction (pull) of a radon-free test solution from a single well. In the presence of DNAPL, radon concentrations during the pull phase are retarded, with retardation manifested in greater dispersion of radon concentrations relative to a conservative tracer. The utility of these methods was investigated in the laboratory using a physical aquifer model (PAM). Static and push-pull tests were performed before and after contamination of the PAM sediment pack with trichloroethene (TCE), and after alcohol cosolvent flushing and pump-and-treat remediation. Numerical simulations were used to estimate the retardation factor for radon in push-pull tests. Radon partitioning was observed in static and push-pull tests conducted after TCE contamination. Calculated TCE saturations ranged up to 1.4% (static test) and 14.1% (push-pull test). Post-remediation tests showed decreases in TCE saturations. The results show that radon is sensitive to changes in DNAPL saturation in space and time. However, the methods are sensitive to DNAPL saturation heterogeneity, test location, sample size, and test design. The influence of these factors on test results, as well as the apparent overestimation of the retardation factor in push-pull tests, warrant further investigation.     

Stratigraphic Trapping of Spilled Jet Fuel Beneath the Water Table

Environmental conditions and the initial attempt to recover JP-4 jet fuel from a shallow aquifer at a tank farm in Hanahan, South Carolina, in 1975. allowed the jet fuel to become stratigraphically trapped below the water table. The trapped jet fuel remained an undetected source of dissolved hydrocarbon contamination in shallow ground water in the area for 17 years. The trapped jet fuel was located when a variety of chemical, hydrologic. geologic, and historical evidence led investigators to install and sample deeper wells. These findings emphasize the need to use an integrated approach lo evaluating the data when determining the extent of contamination and planning fuel recovery operations in a lithologically heterogeneous aquifer.     

A mechanism for anomalous decline in radon precursory to an earthquake

Mechanisms for interpreting anomalous decreases in radon in ground water prior to earthquakes are examined with the help of a case study to show that radon potentially is a sensitive tracer of strain changes in the crust preceding an earthquake. The 2003 Chengkung earthquake of magnitude (M) 6.8 on December 10, 2003, was the strongest earthquake near the Chengkung area in eastern Taiwan since 1951. The Antung radon-monitoring station was located 20 km from the epicenter. Approximately 65 d prior to the 2003 Chengkung earthquake, precursory changes in radon concentration in ground water were observed. Specifically, radon decreased from a background level of 780 pCi/L to a minimum of 330 pCi/L. The Antung hot spring is situated in a fractured block of tuffaceous sandstone surrounded by ductile mudstone. Given these geological conditions, we hypothesized that the dilation of brittle rock mass occurred at a rate faster than the recharge of pore water and gas saturation developed in newly created cracks preceding the earthquake. Radon partitioning into the gas phase may explain the anomalous decrease of radon precursory to the 2003 Chengkung earthquake. To support the hypothesis, vapor-liquid, two-phase radon-partitioning experiments were conducted at formation temperature (60 degrees C) using formation brine from the Antung hot spring. Experimental data indicated that the decrease in radon required a gas saturation of 10% developed in rock cracks. The observed decline in radon can be correlated with the increase in gas saturation and then with the volumetric strain change for a given fracture porosity.     

氡预报地震的实验研究

有关氡气的来源、变化机制及共和地应力的关系尚处于研究过程中。本文将围绕这一问题对岩石标本进行压力试验和溶解试验,为氡预报地震的压溶机制提供实验依据。作者在对唐山地区水氡普查测定的基础上,采集井孔围岩及岩芯标本,开展岩石铀(钍)含量、岩石压氡、岩石水溶解氡及井孔水氡含量之间的综合研究。初步认为,当岩石受压变形破裂时井孔围岩中放射性元素的含量与氡逸出量呈正向关系     

Delineation of regional arid karstic aquifers: an integrative data approach

This research integrates data procedures for the delineation of regional ground water flow systems in arid karstic basins with sparse hydrogeologic data using surface topography data, geologic mapping, permeability data, chloride concentrations of ground water and precipitation, and measured discharge data. This integrative data analysis framework can be applied to evaluate arid karstic aquifer systems globally. The accurate delineation of ground water recharge areas in developing aquifer systems with sparse hydrogeologic data is essential for their effective long-term development and management. We illustrate the use of this approach in the Cuatrociénegas Basin (CCB) of Mexico. Aquifers are characterized using geographic information systems for ground water catchment delineation, an analytical model for interbasin flow evaluation, a chloride balance approach for recharge estimation, and a water budget for mapping contributing catchments over a large region. The test study area includes the CCB of Coahuila, Mexico, a UNESCO World Biosphere Reserve containing more than 500 springs that support ground water-dependent ecosystems with more than 70 endemic organisms and irrigated agriculture. We define recharge areas that contribute local and regional ground water discharge to springs and the regional flow system. Results show that the regional aquifer system follows a topographic gradient that during past pluvial periods may have linked the Río Nazas and the Río Aguanaval of the Sierra Madre Occidental to the Río Grande via the CCB and other large, currently dry, upgradient lakes.     

Thermomagnetic characteristics in late orogenic granites and gneisses of the southern Appalachian Piedmont

Thermomagnetic curves have been obtained for samples from 25 granites and gneisses in Georgia, South Carolina, and North Carolina. This data set can be divided into two distinct curve types: Type I includes rocks which exhibit no distinct Curie points and a linear decrease in magnetization with increasing temperature; Type II curves exhibit a distinct Curie point over a range of temperatures expected for magnetite (500–580°C). Synthetic samples constructed from magnetite and hematite powder exhibit Type I behavior when the hematite to magnetite ratio is high (e.g. 15 : 1). Examination of polished sections shows relatively coarse-grained magnetite only in Type II rocks. We interpret our data to indicate that Type I thermomagnetic curves are dominated by relatively large hematite/magnetite ratios while Type II granites are characterized by relatively coarse-grained magnetite. Type I granite samples have low magnetic susceptibility values (less than 4 × 10^?4 cgs) while most Type II granite samples have higher values. The Type I granites are invariably¹⁸O-enriched whereas Type II granites typically exhibit low¹⁸O/¹⁶O ratios. These relationships are consistent with previously reported correlations of susceptibility (generally indicative of magnetite content) and oxygen isotopic trends in the southern Appalachian Piedmont.     

MTBE and gasoline hydrocarbons in ground water of the United States

The occurrence of methyl tert-butyl ether (MTBE) and gasoline hydrocarbons was examined in three types of studies of ground water conducted by the U.S. Geological Survey: major aquifer surveys, urban land-use studies, and agricultural land-use studies. The detection frequency of MTBE was dependent on the study type, with the highest detection frequency in urban land-use studies. Only 13 ground water samples from all study types, or 0.3%, had concentrations of MTBE that exceeded the lower limit of the U.S. EPA's Drinking-Water Advisory. The detection frequency of MTBE was highest in monitoring wells located in urban areas and in public supply wells. The detection frequency of any gasoline hydrocarbon also was dependent on study type and generally was less than the detection frequency of MTBE. The probability of detecting MTBE in ground water was strongly associated with population density, use of MTBE in gasoline, and recharge. Ground water in areas with high population density, in areas where MTBE is used as a gasoline oxygenate, and in areas with high recharge rates had a greater probability of MTBE occurrence. Also, ground water from public supply wells and shallow ground water underlying urban land-use areas had a greater probability of MTBE occurrence compared to ground water from domestic wells and ground water underlying rural land-use areas. The probability of detecting MTBE in ground water was weakly associated with the density of leaking underground storage tanks, soil permeability, and aquifer consolidation, and only concentrations of MTBE >0.5 microg/L were associated with dissolved oxygen.     

Impact of Turbidity on TCE and Degradation Products in Ground Water

Elevated particulate concentrations in ground water samples can bias contaminant concentration data. This has been particularly problematic for metal analyses where artificially increased turbidity levels can affect metals concentrations and confound interpretation of the data. However, few studies have been conducted to determine the impact of particulates on trichloroethylene (TCE), cis-dichloroethylene (c-DCE), and vinyl chloride concentrations.
Laboratory batch studies and field investigations were conducted to evaluate the effects of suspended solids on VOC concentrations in ground water samples analyzed by purge-and-trap gas chromatography. Three different solids were used to assess the effects of suspended particulates. The solids were aquifer material from a field site in North Carolina and two reference clay minerals (kaolinite and Namontimorillonite). During the laboratory portion of this study, the solids were used to determine effects on TCE concentrations under controlled laboratory conditions.
The same solids were used in a field study to compare the laboratory results with field results. Solids were added to the sample vials prior it) sample collection to intentionally increase turbidity levels in the water samples. Results of the study indicate essentially no decrease in TCE, c-DCH, or vinyl chloride concentrations due to increased turbidity levels.     

The permeability of the Elkhorn fault zone,South Park,Colorado

The purposes of this study are to use both field and modeling approaches to characterize the permeability of a fault and to assess the role of the fault on regional ground water flow. The study subject is the Elkhorn fault, a low-angle reverse fault that brings Precambrian crystalline rocks over the sediments of Colorado's South Park Basin. The fault is hypothesized to act as a low-permeability barrier to flow, restricting interaction between the crystalline aquifer and the basin sediments. To test this hypothesis and to better predict the permeability structure of the fault, we synthesized geologic data to create a geologic model of the fault, conducted aquifer tests to estimate the hydrogeologic properties of the fault zone, and used ground water modeling to test the influence of a range of hydraulic properties for the fault zone on ground water flow in the region. Our study suggests that the fault is a low-permeability feature. Estimated heads are best matched to observations by modeling the fault as a 10-foot-thick interval of low-permeability fault gouge. Steady-state flow models show that much of the flow in the study area is topographically driven near land surface. Flow rates decrease with depth in the aquifers. In the footwall, ground water moves updip in the Michigan-San Isabel syncline to discharge in the South Park Basin. In the hanging wall, ground water moves east to a regional ground water divide. Sensitivity analyses indicate that hydraulic heads are most sensitive to changes in hydraulic conductivity and recharge.     

Development of saline ground water through transpiration of sea water

As vegetation usually excludes salt during water uptake, transpiration will increase the salinity of the residual water. If the source water is sea water, then the residual water may become highly saline. In the unconfined coastal aquifer of the tropical Burdekin River delta, northeastern Australia, areas of highly saline ground water with chloride concentrations up to almost three times that of sea water occur up to 15 km from the present coastline, and are attributed to transpiration by mangrove vegetation during periods of high sea level. Radiogenic ((14)C) carbon isotope analyses indicate that ground water with chloride concentrations between 15,000 and 35,000 mg/L is mostly between 4000 and 6000 years old, at which time sea level was 2 to 3 m higher than present. Stable isotope analyses of oxygen-18 and deuterium show no evidence for evaporative enrichment of this water. Oxygen-18, deuterium, and stable (delta(13)C) carbon isotope analyses of ground water and soil water point to a recharge environment beneath the mangrove forests during this postglacial sea level high stand. During that period, transpiration of the mangrove forests would have led to high chloride concentrations in the residual ground water, without inducing isotopic fractionation. Due to the higher density, this hypersaline water moved downward through the aquifer by gravity and has formed lenses of highly saline ground water at the bottom of the unconfined aquifer.     

Influence of fracture anisotropy on ground water ages and chemistry,Valley and Ridge province,Pennsylvania

Model ground water ages based on chlorofluorocarbons (CFCs) and tritium/helium-3 (³H/³He) data were obtained from two arrays of nested piezometers located on the north limb of an anticline in fractured sedimentary rocks in the Valley and Ridge geologic province of Pennsylvania. The fracture geometry of the gently east plunging fold is very regular and consists predominately of south dipping to subhorizontal to north dipping bedding-plane parting and east striking, steeply dipping axial-plane spaced cleavage. In the area of the piezometer arrays, which trend north-south on the north limb of the fold, north dipping bedding-plane parting is a more dominant fracture set than is steeply south dipping axial-plane cleavage. The dating of ground water from the piezometer arrays reveals that ground water traveling along paths parallel to the dip direction of bedding-plane parting has younger ³H/³He and CFC model ages, or a greater component of young water, than does ground water traveling along paths opposite to the dip direction. In predominantly unmixed samples there is a strong positive correlation between age of the young fraction of water and dissolved sodium concentration. The travel times inferred from the model ages are significantly longer than those previously calculated by a ground water flow model, which assumed isotropically fractured layers parallel to topography. A revised model factors in the directional anisotropy to produce longer travel times. Ground water travel times in the watershed therefore appear to be more influenced by anisotropic fracture geometry than previously realized. This could have significant implications for ground water models in other areas underlain by similarly tilted or folded sedimentary rock, such as elsewhere in the Valley and Ridge or the early Mesozoic basins.     

Effects of water use on arsenic release to well water in a confined aquifer

Field-based experiments were designed to investigate the release of naturally occurring, low to moderate (< 50 microg/L) arsenic concentrations to well water in a confined sandstone aquifer in northeastern Wisconsin. Geologic, geochemical, and hydrogeologic data collected from a 115 m2 site demonstrate that arsenic concentrations in ground water are heterogeneous at the scale of the field site, and that the distribution of arsenic in ground water correlates to solid-phase arsenic in aquifer materials. Arsenic concentrations in a test well varied from 1.8 to 22 microg/L during experiments conducted under no, low, and high pumping rates. The quality of ground water consumed from wells under typical domestic water use patterns differs from that of ground water in the aquifer because of reactions that occur within the well. Redox conditions in the well can change rapidly in response to ground water withdrawals. The well borehole is an environment conducive to microbiological growth, and biogeochemical reactions also affect borehole chemistry. While oxidation of sulfide minerals appears to release arsenic to ground water in zones within the aquifer, reduction of arsenic-bearing iron (hydr)oxides is a likely mechanism of arsenic release to water having a long residence time in the well borehole.     

Influence of ancient thrust faults on the hydrogeology of the Blue Ridge Province

The Blue Ridge Province contains ubiquitous northeast-southwest-trending thrust faults or smaller thrust "slivers" that greatly impact the nature and character of ground water flow in this region. Detailed investigations at a field site in Floyd County, Virginia, indicate that high-permeability zones occur in the brittle crystalline rocks above these thrust faults. Surface and borehole geophysics, aquifer tests, and chlorofluorocarbon and geochemical data reveal that the shallow saprolite aquifer is separated from the deeper fault-zone aquifer by a low-fracture permeability bedrock confining unit, the hydraulic conductivity of which has been estimated to be six orders of magnitude less than the conductivity of the fault zones at the test site. Within the Blue Ridge Province, these fault zones can occur at depths of 300 m or more, can contain a significant amount of storage, and yield significant quantities of water to wells. Furthermore, it is expected that these faults may compartmentalize the deep aquifer system. Recharge to and discharge from the deep aquifer occurs by slow leakage through the confining unit or through localized breach zones that occur where quartz accumulated in high concentrations during metamorphism and later became extensively fractured during episodes of deformation. The results of this investigation stress the importance of thrust faults in this region and suggest that hydrogeologic models for the Blue Ridge Province include these ancient structural features. Faults in crystalline-rock environments may not only influence the hydrology, they may dominate the flow characteristics of a region.     

地热异常区不同含水层水化学组分差异

对天津周良庄地热区不同含水层水化学背景开展实验研究,结果发现：随含水层埋藏深度加大,气体组分变化较大,水氡、水汞、离子组分变化较平稳,水氡背景值偏低.在此基础上,从含水层岩性、取样条件、水化学组分特性、地质构造等方面,对不同含水层之间水化学组分的差异性进行分析,认为区域内特殊地质构造是影响差异性的重要因素.     

Radiocarbon and δ13C Values Related to Ground-Water Recharge and Mixing

Ground-water levels in the Upper Floridan aquifer beneath the southeastern coast of South Carolina have undergone pumpage-induced declines approaching 20 ft below sea level at the southern end of Hilton Head Island. This scenario suggests the potential exists for the inducement of recharge to the Upper Floridan aquifer across the island, which could affect the quality of water being pumped by wells. However, low radiocarbon concentrations in ground-water samples (0.5 to 1.4 ± 0.1 PMC) indicate that most of the water is relict ground water reflecting prepumpage ground-water flow conditions in the Upper Floridan aquifer. The isotopic data indicate long residence times and water-chemistry evolution more characteristic of ground-water recharge occurring farther inland prior to the commencement of pumpage in the late 1800s. Radiocarbon concentrations (as Percent Modern Carbon) and stable carbon isotope ratios (as δ¹³C in dissolved inorganic carbon) determined during this study and reported in other studies on and around Hilton Head Island varied in a systematic manner. Heavier δ¹³C values (–2.8 to –1.6 per mil) in ground water beneath southern Hilton Head Island reflect ground-water discharge from prepumpage flowpaths originating over 100 miles away, hence a depletion in radiocarbon concentration with corrected ground-water ages no younger than 16,000 yrs BP. In contrast, lighter δ¹³C values (–13.9 to –8.67 per mil) beneath the northern part of the island indicate recent recharge as a result of water-level declines, and recharge in areas off the island that have not changed as a result of pumpage (evidenced by enrichment in radiocarbon with corrected ground-water ages no older than 4,000 yrs BP). This suggests that the δ¹³C composition of ground water in the Upper Floridan aquifer is a useful indicator of mixing between ground waters from different sources, and can be used to delineate recharge-discharge patterns. This approach may be applicable to other aquifers of highly evolved ground-water chemistry in regional carbonate aquifer systems that may be receiving recent recharge. Moreover, this approach could prove useful in delineating the contribution of recent water being captured by pumped wells as part of wellhead protection programs designed to assess aquifer vulnerability from surficial contaminant sources.     

Iron and Manganese in Groundwater: Using Kriging and GIS to Locate High Concentrations in Buncombe County,North Carolina

For health, economic, and aesthetic reasons, allowable concentrations (as suggested by the United States Environmental Protection Agency) of the secondary contaminants iron (Fe) and manganese (Mn) found present in drinking water are 0.3 and 0.05 mg/L, respectively. Water samples taken from private drinking wells in rural communities within Buncombe County, North Carolina contain concentrations of these metals that exceed secondary water quality criteria. This study predicted the spatial distribution of Fe and Mn in the county, and evaluated the effect of site environmental factors (bedrock geology, ground elevation, saprolite thickness, and drinking water well depth) in controlling the variability of Fe and Mn in groundwater. A statistically significant correlation between Fe and Mn concentrations, attributable to bedrock geology, was identified. Prediction models were created using ordinary kriging and cokriging interpolation techniques to estimate the presence of Fe and Mn in groundwater where direct measurements are not possible. This same procedure can be used to estimate the trend of other contaminants in the groundwater in different areas with similar hydrogeological settings.     

Geochemical precursors to seismic activity

Studies of earthquake precursory phenomena during the last several decades have found that significant geophysical and geochemical changes can occur prior to intermediate and large earthquakes. Among the more intensely investigated geochemical phenomena have been: (1) changes in the concentrations of dissolved ions and gases in groundwaters and (2) variations in the concentrations of crustal and mantle volatiles in ground gases. The concentration changes have typically showed no conanomalies trend (either increasing or decreasing), and the spatial and temporal distribution of the observed anomalies have been highly variable. As a result, there is little agreement on the physical or chemical processes responsible for the observed anomalies. Mechanisms proposed to account for precursory groundwater anomalies include ultrasonic vibration, pressure sensitive solubility, pore volume collapse, fracture induced increases in reactive surfaces, and aquifer breaching/fluid mixing. Precursory changes in soil gas composition have been suggested to result from pore volume collapse, micro-fracture induced exposure of fresh reactive silicate surfaces, and breaching of buried gas-rich horizons. An analysis of the available field and laboratory data suggests that the aquifer breaching/fluid mixing (AB/FM) model can best account for many of the reported changes in temperature, dissolved ion and dissolved gas concentrations in groundwater. Ultrasonic vibration and pressure sensitive solubility models cannot reasonably account for the geochemical variations observed and, although the pore collapse model could explain some of the observed chemical changes in groundwater and ground gas, uncertainties remain regarding its ability to generate anomalies of the magnitude observed. Other geochemical anomalies, in particular those associated with hydrogen and radon, seem best accounted for by increases in reactive surface areas (IRSA model) that may accompany precursory deformation around the epicenter of an impending earthquake. Analysis of the probable response of these models to the earthquake preparation process, as well as to other environmental factors, suggests that geochemical monitoring programs can provide information that may be valuable in forecasting the probability of an earthquake; however, because of the complexity of the earthquake preparation process, the absolute prediction of seismic events using geochemical methods alone, does not presently appear to be feasible.     

Evidence for Enhanced Mineral Dissolution in Organic Acid-Rich Shallow Ground Water

Total concentrations of formate, acetate, and isobutyrate varied from less than 5 to greater than 9,000 μmol/l over distances of < 3 m in ground water from a shallow hydrocarbon contaminated aquifer. Laboratory incubations of aquifer material indicate that organic acid concentrations were dependent on the amount of hydrocarbon loading in the sediment and the relative rates of microbial organic acid production and consumption. In heavily contaminated sediments, production greatly exceeded consumption and organic acid concentrations increased. In lightly contaminated sediments rates were essentially equal and organic acid concentrations remained low. Concentrations of dissolved calcium, magnesium, and iron generally were one to two orders of magnitude higher in organic acid-rich ground water than in ground water having low organic acid concentrations. Carbonate and Fe(III)-oxyhydroxide minerals were the likely sources of these elements. Similarly, concentrations of dissolved silica, derived from quartz and k-feldspar, were higher in organic acid-rich ground water than in other waters. The positive relation (r = 0.60, p < .05, n = 16) between concentrations of silica and organic acids suggests that the microbially mediated buildup of organic acids in ground water enhanced quartz/k-feldspar dissolution in the aquifer, although it was not the only factor influencing their dissolution. A model that included organic acid microequivalents normalized by cation microequivalents significantly strengthened the correlation (r = 0.79, p < .001, n = 16) between dissolved silica and organic acid concentrations, indicating that competition between silica and cations for complexation sites on organic acids also influenced quartz/k-feldspar dissolution. Physical evidence for enhanced mineral dissolution in organic acid-rich waters included scanning electron microscopy images of highly corroded quartz and k-feldspar grains from portions of the aquifer containing organic acid-rich ground water. Microporosity generated in hydrocarbon contaminated sediments may adversely affect remediation efforts that depend on the efficient injection of electron acceptors into an aquifer or on the recovery of solutes from an aquifer.