Recommended Sampling Intervals for Arsenic in Private Wells

Geogenic arsenic in drinking water is a worldwide problem. For private well owners, testing (e.g., private or government laboratory) is the main method to determine arsenic concentration. However, the temporal variability of arsenic concentrations is not well characterized and it is not clear how often private wells should be tested. To answer this question, three datasets, two new and one publicly available, with temporal arsenic data were utilized: 6370 private wells from New Jersey tested at least twice since 2002, 2174 wells from the USGS NAWQA database, and 391 private wells sampled 14 years apart from Bangladesh. Two arsenic drinking water standards are used for the analysis: 10 µg/L, the WHO guideline and EPA standard or maximum contaminant level (MCL) and 5 µg/L, the New Jersey MCL. A rate of change was determined for each well and these rates were used to predict the temporal change in arsenic for a range of initial arsenic concentrations below an MCL. For each MCL and initial concentration, the probability of exceeding an MCL over time was predicted. Results show that to limit a person to below a 5% chance of drinking water above an MCL, wells that are ½ an MCL and above should be tested every year and wells below ½ an MCL should be tested every 5 years. These results indicate that one test result below an MCL is inadequate to ensure long-term compliance. Future recommendations should account for temporal variability when creating drinking water standards and guidance for private well owners.     

The Utility of Multiple-Completion Monitoring Wells for Describing a Solvent Plume

At a study site in the midwestern United States, multiple-completion wells demonstrated that a vertical hydraulic gradient was responsible for the contamination pattern exhibited by chlorinated solvent plumes. The typical pattern consisted of little or no contamination in the upper portion of the aquifer with concentrations increasing with depth. When ground water contamination was discovered in an unexpected portion of the site, water level elevations and contaminant distribution data obtained from multiple-completion wells resulted in identification of the source location. The well eventually determined to be located in the source area displayed contaminant levels much higher in the upper zone of the aquifer — the opposite contamination pattern of other on-site wells. Such results indicated that the spill had occurred near this location and that solvent residing along the capillary fringe was continuing to contaminate the aquifer.     

Naturally Occurring Arsenic in Sandstone Aquifer Water Supply Wells of Northeastern Wisconsin

The U.S. Environmental Protection Agency (EPA) maximum contaminant level (MCL) of 50 μg/L for arsenic was exceeded in 86 of 2125 water supply wells sampled over a broad geographic range in pails of Drown. Outagamie and Winnebago Counties, Wisconsin. The hydrologic and geochemical properties of the area were examined and the source of arsenic was determined to be natural, Ground water collected from two geologic formations, the St. Peter Sandstone and the overlying Platteville/Galena Dolomite, was found to be the principal source of the elevated arsenic concentrations. These two Formations supply a large portion of eastern Wisconsin private wells with their drinking water.
Three wells were found within Outagamie County to have an unusually low pH. Results suggest that the cause of the low pH in these wells is of natural origin induced by the oxidation of iron sulfide minerals. In this reaction iron sulfide minerals are oxidized. forming sulfuric acid causing a low pH and a high concentration of various metals to leach from native rock formations into the water supply.
Based on the data gathered from this study, an arsenic advisory area was designated for both Outagamie and Winnebago Counties. Guidelines were developed for well drillers and owners constructing new wells within the advisory area to reduce the likelihood of arsenic presence in the water supply. Fifteen wells containing arsenic exceeding the MCL were successfully reconstructed or new wells were constructed based on the guidelines developed. These constructions substantially reduced arsenic levels in the well water supplies.     

Organic Halogen Group Parameters as Indicators of Ground Water Contamination

A regional survey of Danish ground water demonstrated the presence of adsorbable organic halogens (AOX) in almost all of 142 wells (99 percent). Generally, the presence of AOX was not related to point or non-point source contamination with halogenated organics. However, the AOX concentrations varied with the geology of the aquifers. Extractable organic halogens (EOX) and volatile organic halogens (VOX) were far less prevalent (detected in 4 percent of sampled wells) and the detection could, in most cases, be explained by contamination or chlorination of the wells. The VOX concentrations corresponded to the concentrations of identified, volatile contaminants. The study demonstrates the presence of a natural background level of AOX in the investigated aquifers. This must be considered in the interpretation of AOX results as an indicator of ground water contamination with haloorganics. Similar background levels of EOX or VOX were not delected.     

Temporal changes in water quality at a childhood leukemia cluster

Since 1997, 15 cases of acute lymphocytic leukemia and one case of acute myelocytic leukemia have been diagnosed in children and teenagers who live, or have lived, in an area centered on the town of Fallon, Nevada. The expected rate for the population is about one case every five years. In 2001, 99 domestic and municipal wells and one industrial well were sampled in the Fallon area. Twenty-nine of these wells had been sampled previously in 1989. Statistical comparison of concentrations of major ions and trace elements in those 29 wells between 1989 and 2001 using the nonparametric Wilcoxon signed-rank test indicate water quality did not substantially change over that period; however, short-term changes may have occurred that were not detected. Volatile organic compounds were seldom detected in ground water samples and those that are regulated were consistently found at concentrations less than the maximum contaminant level (MCL). The MCL for gross-alpha radioactivity and arsenic, radon, and uranium concentrations were commonly exceeded, and sometimes were greatly exceeded. Statistical comparisons using the nonparametric Wilcoxon rank-sum test indicate gross-alpha and -beta radioactivity, arsenic, uranium, and radon concentrations in wells used by families having a child with leukemia did not statistically differ from the remainder of the domestic wells sampled during this investigation. Isotopic measurements indicate the uranium was natural and not the result of a 1963 underground nuclear bomb test near Fallon. In arid and semiarid areas where trace-element concentrations can greatly exceed the MCL, household reverse-osmosis units may not reduce their concentrations to safe levels. In parts of the world where radon concentrations are high, water consumed first thing in the morning may be appreciably more radioactive than water consumed a few minutes later after the pressure tank has been emptied because secular equilibrium between radon and its immediate daughter progeny is attained in pressure tanks overnight.     

Monitoring well interception with fractures in clayey till

When using monitoring wells for investigation of contaminant sources in clayey till, there is a high risk that fractures may cause mobile contaminants to bypass the monitoring wells. This paper indicates that the probability of interception between monitoring wells and hydraulic conductive fractures is often significantly less than 50%. Based on a field experiment and application of a calibrated discrete fracture matrix diffusion numerical model (FRAC3Dvs), the paper also evaluates pesticide-monitoring results for different positions of monitoring well screen relative to fractures. For well screens situated 0.25 and 2 m from a conductive fracture, the first concentrations of the pesticide metabolite (2,6 dichlorobenzamide, "BAM") would be measured two years and 18 years, respectively, after the contaminant had been transported into an underlying aquifer. In this way, underlying aquifers may be subjected to contamination by downward moving contamination without being observed in monitoring wells in the till.     

Temporal Changes in VOC Discharge to Surface Water from a Fractured Rock Aquifer During Well Installation and Operation, Greenville, South Carolina

Analysis of the vapor in passive vapor samplers retrieved from a streambed in fractured rock terrain implied that volatile organic carbon (VOC) discharge from ground water to surface water substantially increased following installation of a contaminant recovery well using air rotary drilling. The air rotary technique forced air into the aquifer near the stream. The injection produced an upward hydraulic gradient that appears to have transported water and contaminants from deeper parts of the aquifer through fractures into shallow parts of the aquifer. Once in the shallow flow regime, the contamination was transported to the stream, where it discharged during the next several weeks following well installation. After the recovery well was activated and began continuously pumping contaminated ground water to a treatment facility, the VOC concentrations in the stream bottom passive vapor samplers decreased to below detectable concentrations, suggesting that the withdrawal had captured the contaminated ground water that previously had discharged to the stream.     

Techniques and Equipment Used in Contaminant Detection at Hoe Creek Underground Coal Gasification Experimental Site

Data from an existing network of ground water monitoring wells at the U.S. Department of Energy (DOE) Hoe Creek Underground Coal Gasification (UCG) Experimental Site indicated that organic contaminants, particularly phenols produced during gasification experiments, were threatening neighboring ground water resources. The existing monitoring well network was sparse and further definition of the extent and direction of contaminant migration was needed. Additionally, water level data, important in determining flow directions, was incomplete. A field program was designed and implemented to locate and define the organic contamination and expand the existing ground water monitoring program. The program utilized field analysis of phenol for contaminant detection and well location, followed by completion using gas-drive ground water samplers/piezometers. Geophysical logging was used to permit optimum placement of the samplers. The geologic aspects of the site posed some interesting problems to the installation of the samplers. The contaminant plume edge was defined in the east, west and south directions during the field program. Further work is needed in the north direction.     

Groundwater Quality Impacts from a Full‐Scale Integrated Constructed Wetland

The concept of integrated constructed wetlands (ICW) promotes in‐situ soils to construct and line wetland cells. The integrity of soil material, however, may provide a potential pathway for contaminants to flow into the underlying groundwater. This study assessed the extent of groundwater quality deterioration due to the establishment of a full‐scale ICW system treating domestic wastewater in Ireland. The ICW is located at Glaslough in Co. Monaghan, Ireland. It consists of two sedimentation ponds and a sequence of five shallow vegetated wetland cells. The ICW cells were lined with 500‐mm thick local subsoil material, which comprised a mixture of alluvium, organic soils, tills, and gravel. Groundwater samples and head data were collected from eight piezometers, which were installed around the ICW cells. The groundwater and wetland water samples were analysed for water quality parameters such as bulk organic matter, nutrients, and pathogens. Overall, the quality of groundwater underlying the ICW system recorded some contamination with bulk organic matter and some inorganic nutrients. Significantly higher contaminant concentrations were recorded in monitoring wells upgradient and near to the distal wetland cells than downgradient ones, which were near to the proximal cells. For the downgradient piezometers, concentrations seldomly exceeded the natural background levels. Detailed analyses through the application of chemometrics models indicated that the source of contamination was largely of geogenic origin. Findings suggest that ICW systems pose a minimal risk to the groundwater quality; the greatest risk was associated with the distal wetland cells.     

Influence of Casing Materials on Trace-Level Chemicals in Well Water

Four well casing materials — polyvinyl chloride (PVC), polytetrafluoroethylene (PTFE), and stainless steel 304 (SS 304) and 316 (SS 316) — were examined to determine their suitability for monitoring inorganic and organic constituents in well water.
The inorganic study used a factorial design to test the effect of concentration of mixed metals (arsenic [As], chromium [Cr], lead [Pb], and cadmium [Cd]), pH, and organic carbon. Sample times were 0.5, 4, 8, 24, and 72 hours. Except for slow loss of Pb, PTFE well casings had no significant effect on the concentration of metals in solution. For the other casings, changes in analyte concentration often exceeded 10 percent in eight hours or less and, thus, could bias analyses of samples taken from wells constructed with these materials. Specifically, PVC casings sorbed Pb and leached Cd; SS 316 casings sorbed As and Pb and leached Cd; and SS 304 casings sorbed As, Cr, and Pb and leached Cd. Both stainless steel casing materials showed markedly poorer performance than the PVC casings.
The well casings were also tested for sorption/desorption of 10 organic substances from the following classes: chlorinated alkehes, chlorinated aromatics, nitroaromatics and nitramines. Sample times were 0, 1, 8, 24, and 72 hours, seven days, and six weeks. There were no detectable losses of analytes in any of the sample solutions containing stainless steel well casings. Significant loss of some analytes was observed in sample solutions containing plastic casings, although losses were always more rapid with the PTFE casings than with PVC. Chlorinated organic substances were lost most rapidly. For samples containing PTFE casings, losses of some of these compounds were rapid enough (>10 percent in eight hours) to be of concern for ground water monitoring. Losses of hydrophobic organic constituents in samples containing PTFE casings were correlated with the compound's octanol/water partition coefficient.     

Relating nitrogen sources and aquifer susceptibility to nitrate in shallow ground waters of the United States

Characteristics of nitrogen loading and aquifer susceptibility to contamination were evaluated to determine their influence on contamination of shallow ground water by nitrate. A set of 13 explanatory variables was derived from these characteristics, and variables that have a significant influence were identified using logistic regression (LR). Multivariate LR models based on more than 900 sampled wells predicted the probability of exceeding 4 mg/L of nitrate in ground water. The final LR model consists of the following variables: (1) nitrogen fertilizer loading (p-value = 0.012); (2) percent cropland-pasture (p < 0.001); (3) natural log of population density (p < 0.001); (4) percent well-drained soils (p = 0.002); (5) depth to the seasonally high water table (p = 0.001); and (6) presence or absence of a fracture zone within an aquifer (p = 0.002). Variables 1-3 were compiled within circular, 500 m radius areas surrounding sampled wells, and variables 4-6 were compiled within larger areas representing targeted land use and aquifers of interest. Fitting criteria indicate that the full logistic-regression model is highly significant (p < 0.001), compared with an intercept-only model that contains none of the explanatory variables. A goodness-of-fit test indicates that the model fits the data well, and observed and predicted probabilities of exceeding 4 mg/L nitrate in ground water are strongly correlated (r2 = 0.971). Based on the multivariate LR model, vulnerability of ground water to contamination by nitrate depends not on any single factor but on the combined, simultaneous influence of factors representing nitrogen loading sources and aquifer susceptibility characteristics.     

Pump-and-Treat Accomplishments: A Review of the Effectiveness of Ground Water Remediation in Santa Clara Valley, California

Pump and treat has been successful in significantly reducing the volatile organic contaminant concentrations in ground water in Santa Clara Valley. California. The California Regional Water Quality Control Board. San Francisco Bay Region, currently oversees 61 sites in Santa Clara Valley with operating pump-and-treat systems, of which 42 sites have been extracting ground water since at least 1987. This review- evaluates the effects of ground water extraction on contaminant concentrations at 37 of those 42 sites. The evaluation focuses on trichloroethane, trichloroethene, and dichloroethane, as these were the most prevalent contaminants encountered at the sites. The majority of sites obtained greater than 90 percent reduction in maximum concentrations for one or more of the three contaminants. While only one of the 37 sites obtained maximum contaminant levels (MCL) for all contaminants, six of the sites included in the analyses reached MCLs for one or more of the sampled contaminants, and an additional seven of the sites are near MCLs for al least one contaminant. Our findings indicate that, while pump and treat successfully reduced maximum concentrations al most of the sites reviewed, successful attempts to reduce maximum contaminant concentrations to below MCLs are limited.     

Screened Auger Sampling: The Technique and Two Case Studies

The screened auger is a laser-slotted, hollow-stem auger through which a representative sample of ground water is pumped from an aquifer and tested for water-quality parameters by appropriate field-screening methods. Screened auger sampling can be applied to ground water quality remedial investigations, providing:(1) a mechanism for determining a monitoring well's optimal screen placement in a contaminant plume; and (2) data to define the three-dimensional configuration of the contaminant plume.
Screened auger sampling has provided an efficient method for investigating hexavalent chromium and volatile organic compound contamination in two sandy aquifers in Cadillac, Michigan. The aquifers approach 200 feet in thickness and more than 1 square mile in area. A series of screened auger borings and monitoring wells was installed, and ground water was collected at 10-foot intervals as the boreholes were advanced to define the horizontal and vertical distribution of the contaminant plumes. The ability of the screened auger to obtain representative ground water samples was supported by the statistical comparison of field screening results and subsequent laboratory analysis of ground water from installed monitoring wells.     

Passive Samplers for Monitoring VOCs in Groundwater and the Prospects Related to Mass Flux Measurements

Measurement and interpretation of mass fluxes in favor of concentrations is gaining more and more interest, especially within the framework of the characterization and management of large-scale volatile organic carbon (VOC) groundwater contamination (source zones and plumes). Traditional methods of estimating contaminant fluxes and discharges involve individual measurements/calculations of the Darcy water flux and the contaminant concentrations. However, taken into account the spatially and temporally varying hydrologic conditions in complex, heterogeneous aquifers, higher uncertainty arises from such indirect estimation of contaminant fluxes. Therefore, the potential use of passive sampling devices for the direct measurement of groundwater-related VOC mass fluxes is examined. A review of current passive samplers for the measurement of organic contaminants in water yielded the selection of 18 samplers that were screened for a number of criteria. These criteria are related to the possible application of the sampler for the measurement of VOC mass fluxes in groundwater. This screening study indicates that direct measurement of VOC mass fluxes in groundwater is possible with very few passive samplers. Currently, the passive flux meter (PFM) is the only passive sampler which has proven to effectively measure mass fluxes in near source groundwater. A passive sampler for mass flux measurement in plume zones with regard to long-term monitoring (several months to a year) still needs to be developed or optimized. A passive sampler for long-term monitoring of contaminant mass fluxes in groundwater would be of considerable value in the development of risk-based assessment and management of soil and groundwater pollutions.     

Spatial survey of trace metal contaminants in the sediments of the Elizabeth River, Virginia

The Elizabeth River is a sub-estuary of the James River, the most southern tributary of the Chesapeake Bay. It is a highly industrialized area, and has been designated a "toxic hot spot" due to the heavy loads of contaminant metals and organic compounds in its bed sediments. Fifty surface sediment samples were taken along the channels and shoals of the Mainstem and the Southern Branch portions of the river. The samples were analyzed for trace metals (Cd, Cr, Cu, Pb and Zn), Fe and particle properties (% sand, % silt, % clay and specific surface area) to discern the spatial distribution of contaminant metals in this system. Enrichment factors were calculated to assess the overall level of contamination relative to other surrounding waterways as well as historic contamination levels within the river itself. The highest levels of metals were found to be in close proximity to industrial sources of contamination. The overall level of contamination was 3-10 times higher than baseline levels within the river, and 2-3 times higher than contaminant levels in other area waters.     

Vertical Contaminant Profiling of Volatile Organic* in a Deep Fractured Basalt Aquifer

Volatile organic compounds delected in ground water from wells at Test Area North (TAN) at the Idaho National Engineering Laboratory (INEL) prompted RCRA facility investigations in 1989 and 1990 and a CERCLA-driven RI/FS in 1992. In order to address ground water treatment feasibility, one of the main objectives, of the 1992 remedial investigation was to determine the vertical extent of ground water contamination, where the principle contaminant, of concern is trichloroethylene (TCE). It was hypothesized that a sedimentary interbed at depth in the fractured basalt aquifer could be inhibiting vertical migration of contaminants to lower aquifers. Due to the high cost of drilling and installation of ground water monitoring wells at this facility (greater than $100,000 per well), a real time method was proposed for obtaining and analyzing ground water samples during drilling to allow accurate placement of well screens in zones of predicted VOC contamination. This method utilized an inflatable pump packer pressure transducer system interfaced with a datalogger and PC at land surface. This arrangement allowed for real lime monitoring of hydraulic head above and below the packer to detect leakage around the packer during pumping and enabled collection of head data during pumping for estimating hydrologic properties. Analytical results were obtained in about an hour from an on-site mobile laboratory equipped with a gas chromalograplvmass spectrometer (GC/MS). With the hydrologic and analytical results in hand, a decision was made to either complete the well or continue drilling to the next test zone. In almost every case, analytical results of ground water samples taken from the newly installed wells closely replicated the water quality of ground water samples obtained through the pump packer system.     

Field Comparison of Micropurging vs. Traditional Ground Water Sampling

Micropurge sampling of ground water wells has been suggested as a possible replacement to traditional purge and sample methods. To compare methods, duplicate ground water samples were collected at two field sites using iraditional and micropurge methods. Samples were analyzed for selected organic and inorganic constituents, and the results were compared statistically. Analysis of the data using the nonparametric sign test indicates that within a 95 percent confidence interval, there was no significant difference between the two methods for the site contaminants and the majority of analytes. These analytical results were supported by visual observations with the colloidal borescope, which demonstrated impacts on the flow system in the well when using traditional sampling methods. Under selected circumstances, the results suggest replacing traditional sampling with micropurging based on reliability, cost, and waste minimization.     

Low-Flow Purging and Sampling of Ground Water Monitoring Wells with Dedicated Systems

A field study was conducted to assess purging requirements for dedicated sampling systems in conventional monitoring wells and for pumps encased in short screens and buried within a shallow sandy aquifer. Low-flow purging methods were used, and wells were purged until water quality indicator parameters (dissolved oxygen, specific conductance, turbidity) and contaminant concentrations (chromate, trichloroethylene, dichloroethylene) reached equilibrium. Eight wells, varying in depth from 4.6 to 15.2 m below ground surface, were studied. The data show that purge volumes were independent of well depth or casing volumes. Contaminant concentrations equilibrated with less than 7.5 I. of purge volume in all wells. Initial contaminant concentration values were generally within 20 percent of final values. Water quality parameters equilibrated in less than 10 L in all wells and were conservative measures for indicating the presence of adjacent formation water. Water quality parameters equilibrated faster in dedicated sampling systems than in portable systems and initial turbidity levels were lower.     

A Remedial Investigation of an Organically Polluted Outwash Aquifer

A glacial outwash aquifer underlying the Gloucester Landfill near Ottawa, Canada, has become polluted with various organic chemicals following the disposal of laboratory solvents in shallow trenches immediately above the aquifer. Several remedial alternatives have been considered by the government of Canada. Impermeable barrier walls were rejected as being unsuitable given the permeable nature of the underlying bedrock. It appears improbable that pools of liquid organic chemicals (DNAPLs) exist within the aquifer, although ganglia are likely present. Therefore, much of the contaminant plume can be removed hydraulically over a period of five years by the operation of four purge wells discharging to an on-site treatment plant from which the purified water is returned to the aquifer by recharge wells. The residual contamination is anticipated to be cleaned up by in situ biorestoration techniques currently under development.     

Comparison of Fiberglass and Other Polymeric Well Casings, Part I: Susceptibility to Degradation by Chemicals

Previous research has shown that the most commonly used well casing materials-stainless steel. polyvinyl chloride (PVC). and polytetra-fluoroethylene (PTFE)-are not suited for all monitoring environments and applications. This study is part of a series of experiments that were conducted to determine the suitability of four other polymeric well casing materials-acrylonitrile butadiene styrene (ABS), fluorinalcd ethylene propylene (FHP), fiberglass-reinlorced epoxy (FRE), and fiberglass-reinforced plastic (FRP)- for use in ground water monitoring wells. In these studies, these four materials were compared with two other commonly used polymeric well casings, PVC and PTFE. Part I of these studies examines the resistance of these materials to degradation by chemicals. Future reports will consider sorption and leaching of organic and metal contaminants.
In this study, the six materials were exposed to 28 neat organic compounds (including one acid) and to extremely acidic and alkaline aqueous solutions for up to 112 days. This was done to simulate the most aggressive environments to which monitoring well casings may be exposed. The casings were observed for changes in weight and signs of physical degradation (swelling, softening, deterioration, or dissolution).
The two fluorinated polymers (FEP and PTFE) were not degraded by any of the lest chemicals. Among the nonfluorinated products tested. FRE was the most inert. Three organic chemicals caused the glass fibers to separate. and two organic solvents caused weight gains exceeding 10 percent. ABS was the most readily degraded material tested. By the end of the study, only the acid and alkaline solutions had little effect on ABS. FRP was more severely degraded by the organic chemicals than FRH but was less affected than PVC. FRP and FRE. lost weight when exposed to the highly acidic conditions.