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Marcel Belaval

Publications and source records attributed to Marcel Belaval.

11 recordsLinked to original sources

Linking stream-reach nitrogen loads and groundwater “reachsheds” to inform wastewater-nitrogen management actions, Cape Cod, Massachusetts

Study Region Cape Cod, Massachusetts, U.S.A. Study Focus Anthropogenic nitrogen (N) is a key factor in degrading groundwater and surface-water quality, particularly in coastal New England where onsite wastewater systems are prevalent. This study evaluated whether direct N-load measurements in streams on Cape Cod, Massachusetts, coupled with flow-path information from groundwater-flow models, can effectively identify potential land areas where nitrogen mitigation could substantially reduce loads to receiving waters. Nitrogen fluxes were measured along 63 stream reaches during winter and summer and paired with simulated groundwater recharge areas to identify and rank potential areas for reduction of nonpoint-source N inputs. New Hydrologic Insights for the Region Reach-scale nitrate-N loads ranged from −39.1–1182 kg-N/yr per 100 m of stream, indicating spatially variable groundwater inputs across seasons. “Reachsheds” — areas contributing groundwater recharge to specific stream reaches — were delineated using a regional groundwater-flow model. Strong correlations were found between observed N loads and land-use characteristics, especially the number of septic systems and total N inputs from the sum of considered sources. Observed N loads were moderately correlated with recharge area size and wastewater flow estimates. Correlating reach-specific groundwater N loads with land use and parcel-scale nitrogen-yield data identified reachsheds with the highest potential for N load reduction. This approach enables targeted implementation of restoration efforts to optimize nutrient management and support regional load reduction.

Massachusetts↗

Evaluating the effects of replacing septic systems with municipal sewers on groundwater quality in a densely developed coastal neighborhood, Falmouth, Massachusetts, 2016–19

Land disposal of sewage wastewater through septic systems and cesspools is a major cause of elevated concentrations of nitrogen in the shallow coastal aquifers of southern New England. The discharge of nitrogen from these sources at the coast is affecting the environmental health of coastal saltwater bodies. In response, local, State, and Federal agencies are considering expensive actions to mitigate these effects, including installing municipal sewer systems. To increase the understanding of the effects of municipal sewering on groundwater quality discharging to coastal surface waters, a network of multilevel monitoring wells was established in a densely developed coastal neighborhood on the Maravista peninsula, Falmouth, Massachusetts, which was undergoing conversion from onsite septic disposal to municipal sewering. The geohydrology of the study area on the peninsula is generally characterized as consisting of fine to coarse, well-sorted sands containing 2.9 to 9.3 meters of fresh groundwater and a flow system characterized by a groundwater divide slightly west of the center of the peninsula. The magnitude of hydraulic gradients at the water table is gently sloping, ranging from 0.000032 to 0.00059, and affected by daily and bimonthly tidal fluctuations from adjacent coastal ponds. On the western side of the divide, upgradient from Little Pond, average linear groundwater velocities and traveltimes along shallow flow paths, estimated from observed hydraulic gradients and estimated aquifer hydraulic conductivity and effective porosity, range from 0.076 to 0.094 meters per day and 7.8 to 9.7 years, respectively. The groundwater monitoring network consists of 14 profile sites on the peninsula that each include a multilevel sampler for water-quality data collection and a shallow monitoring well for groundwater-level measurements. The study area encompasses about 230 residences that transitioned from onsite septic disposal to municipal sewering between spring 2017 and summer 2019. An additional multilevel sampler that was in a residential coastal setting but not undergoing sewering also was sampled periodically as a reference site. Elevated nitrogen, as compared to typical uncontaminated, fresh groundwater in the Cape Cod aquifer, predominately as nitrate, was measured in 15 water-quality profiles at nitrate concentrations as great as 26.2 milligrams per liter as nitrogen ( n =749; mean and median values were 5.1 and 4.1 milligrams per liter as nitrogen, respectively). At all 14 profile sites and the reference profile site on a nearby peninsula, wastewater effects were denoted by increased nitrate, boron, and specific conductance, and by decreased pH and dissolved oxygen. The highest concentrations of nitrate typically occurred in the deepest one-half of the freshwater zone and in intervals of suboxic and oxic groundwater. Thickness-weighted mean and maximum nitrate concentrations, and total nitrate mass from four sampling rounds, provided a metric to evaluate expected changes at the 14 profile sites on the peninsula. Nitrate concentrations varied moderately by site between sampling rounds through both the presewering (June 2016 and April 2017) and transitional periods (April 2018 and June 2019). Nitrate concentrations greater than the U.S. Environmental Protection Agency maximum contaminant level for nitrate in drinking water (10 milligrams per liter as nitrogen), were detected at 9 of the 14 profile sites and at the reference site. The average of the mean thickness-weighted nitrate concentrations for the four full sampling rounds was greater than 5.0 milligrams per liter as nitrogen at 8 sites (7 profile sites and the reference site) and greater than 8 milligrams per liter as nitrogen at 3 profile sites. The total nitrate mass per square meter of land area at each profile site ranged from 1,830 to 36,800 milligrams per square meter. Nitrate mass flux, across a 500-meter-long section upgradient from Little Pond and covering about 15 percent of the total pond shoreline length, ranged from 124.3 to 192.6 kilograms per year for the four full sampling rounds under three groundwater-flow conditions. The expected improvements in groundwater quality in the freshwater zone should be characterized by decreases in concentrations of dissolved total and inorganic nitrogen and common ions such as boron, chloride, and fluoride. A statistical analysis using the Regional Kendall test for sampling points grouped in specific depth ranges confirmed that water-quality changes were statistically significant in at least one depth group during the 3-year sampling period (nitrate: −0.76 milligram per liter per year; specific conductance: −12.1 microsiemens per centimeter at 25 degrees Celsius per year; dissolved oxygen: 0.82 milligram per liter per year); however, the rate at which the water-quality improvements will result in decreases in nitrate mass loads to the coastal ponds primarily depends on groundwater traveltimes and the rate of flushing of wastewater constituents from the aquifer.

Massachusetts↗

Hydrologic site assessment for passive treatment of groundwater nitrogen with permeable reactive barriers, Cape Cod, Massachusetts

Wastewater disposal associated with rapid population growth and development on Cape Cod, Massachusetts, during the past several decades has resulted in widespread contamination of groundwater with nitrogen. As a result, water quality in many of the streams, lakes, and coastal embayments on Cape Cod is impaired by excess nitrogen. To reduce nitrogen loads to these impaired water bodies, watershed-based planning is currently [2019] underway following a regional strategy, the section 208 areawide water-quality management plan update for Cape Cod. In the updated plan, traditional (sewering) and alternative wastewater management options are under consideration for restoring water quality in impaired surface-water bodies. Permeable reactive barriers, which are reactive zones emplaced below the water table for passive treatment of groundwater contaminants, are one of the alternatives being considered by Cape Cod towns as a potentially cost-effective technology for the removal of nitrogen from groundwater. However, the effectiveness of permeable reactive barriers depends on local conditions, and site-specific hydrologic and water-quality data are needed to inform the decision to install a permeable reactive barrier in a given location. These data are not available in most locations on Cape Cod; consequently, site assessments are needed before selecting this treatment option. To address this need, the U.S. Environmental Protection Agency, U.S. Geological Survey, and Cape Cod Commission formed a technical team in 2015 to develop and evaluate a hydrologic site-assessment approach for permeable reactive barrier installation. The approach developed by the technical team includes a preliminary regional assessment followed by a phased onsite investigation. The approach was intended to provide the hydrologic data needed to make informed decisions on site suitability and to support installation and monitoring should the site be deemed appropriate for a permeable reactive barrier. The factors that were evaluated to characterize local hydrologic conditions and inform site selection included groundwater flow directions and rates, depth to the water table, hydraulic conductivity and degree of heterogeneity of the aquifer, spatial distribution and concentration of nitrate and oxidation-reduction-sensitive constituents, thickness and depth of the treatment zone, distance to downgradient water bodies, and access for drilling and permeable reactive barrier installation. The approach was demonstrated on Cape Cod by conducting a preliminary assessment of 27 sites, from which 5 sites were selected for onsite investigations. Results indicated that the site-assessment approach was successful for screening sites and characterizing the geologic, hydrologic, and water-quality conditions at the sites selected for onsite investigations. Overall, the phased assessment evaluated in this study provided an efficient means of obtaining the hydrologic information needed to determine if a site was suitable for permeable reactive barrier installation on Cape Cod for the passive treatment of nitrogen in groundwater.

Massachusetts↗

Geochemical conditions and nitrogen transport in nearshore groundwater and the subterranean estuary at a Cape Cod embayment, East Falmouth, Massachusetts, 2013–14

Nitrogen transport and transformation were studied during 2013 to 2014 by the U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, in a subterranean estuary beneath onshore locations on the Seacoast Shores peninsula, a residential area in Falmouth, Massachusetts, served by septic systems and cesspools, and adjacent offshore locations in the Eel River, a saltwater embayment connected to the ocean. The field investigation included installation and sampling of clusters of wells and temporary sampling points near a transect extending from about 35 meters (m) onshore to 18 m offshore. The fresh groundwater at the study site formed a lens about 11 m thick at the shoreline that was underlain by saline groundwater. Groundwater flow in the water-table aquifer was oriented northwestward toward the embayment. Nitrate concentrations in the fresh groundwater at a site about 35 m onshore increased in the downward direction from less than 500 micromoles per liter near the water table to about 1,700 micromoles per liter just above the freshwater/saltwater transition zone. Dissolved oxygen was largely absent in the onshore fresh groundwater. Distributions of salinity, dissolved oxygen, and nitrate at the shoreline and offshore generally were similar to those onshore; at some locations, however, shallow saline water was present above the freshwater, and there were scattered occurrences of elevated dissolved oxygen concentrations. Geochemical indicators of nitrate reduction, including concentrations of the reaction product nitrogen gas, stable isotope ratios of nitrate and nitrogen gas, and changes in alkalinity, provided evidence for nitrate reduction in two zones separated vertically by a zone 7–8 m thick with no evidence of nitrate reduction. The shallow nitrate-reduction zone was near the water table in fresh groundwater onshore, where nitrate reduction may be related to particular recharge conditions at nearby sources. The shallow nitrate-reduction zone also may be related to an interval of fine-grained sediments at about the same altitude (−1 to −6 m relative to the National Geodetic Vertical Datum of 1929), where flow is slower and reactive electron donors such as solid organic carbon, iron, or sulfide phases may be present to drive the reduction. The deep nitrate-reduction zone was near the freshwater/saltwater transition zone, where nitrate reduction may be related to mixing of freshwater containing nitrate and saltwater containing dissolved organic carbon and ammonium, or to fine-grained sediments near the transition zone. The maximum amount of nitrate converted to nitrogen gas was estimated to be less than or equal to 300 micromoles per liter in both nitrate-reduction zones. The presence of nitrate and low dissolved oxygen concentrations in the 7–8-meter-thick zone between the shallow and deep nitrate-reduction zones are conditions that could permit nitrate reduction. The absence of evidence of nitrate reduction in the high-nitrate zone may have resulted from the lack of reactive electron donors in that depth interval. The high-nitrate zone dissipated somewhat in the offshore direction, but the current study did not extend far enough to encompass the fresh groundwater discharge area or determine how much of the nitrate was removed prior to discharge. A shallow intertidal saltwater cell was formed during a spring tide by saltwater infiltration during tidal run-up on the beach. Nitrate reduction might have occurred if nitrate-containing fresh groundwater discharging to the estuary mixed with the saltwater containing dissolved organic carbon in this zone, but samples collected from the intertidal saltwater cell during this study were not analyzed for indicators of nitrate reduction. Elevated dissolved oxygen concentrations in fresh groundwater 9 m offshore may indicate that groundwater flow was partly oblique to the sampling transect or that groundwater from a regional flow system was converging under the river near the study area. Flow directions also may have been affected by aquifer heterogeneity such as the shallow fine-grained sediments onshore and at the bottom of the Eel River. Improved understanding of the fate of nitrate in this type of complex setting might be gained by including additional characterization of aquifer heterogeneity and groundwater flow and extending investigations of nitrate reduction to the shallow sediments in the intertidal saltwater cell and adjacent subtidal zone and to locations farther offshore beneath the estuary.

Massachusetts↗

Factors affecting temporal variability of arsenic in groundwater used for drinking water supply in the United States

The occurrence of arsenic in groundwater is a recognized environmental hazard with worldwide importance and much effort has been focused on surveying and predicting where arsenic occurs. Temporal variability is one aspect of this environmental hazard that has until recently received less attention than other aspects. For this study, we analyzed 1245 wells with two samples per well. We suggest that temporal variability, often reported as affecting very few wells, is perhaps a larger issue than it appears and has been masked by datasets with large numbers of non-detect data. Although there was only a slight difference in arsenic concentration variability among samples from public and private wells (p = 0.0452), the range of variability was larger for public than for private wells. Further, we relate the variability we see to geochemical factors&mdash;primarily variability in redox&mdash;but also variability in pH and major-ion chemistry. We also show that in New England there is a weak but statistically significant indication that seasonality may have an effect on concentrations, whereby concentrations in the first two quarters of the year (January&ndash;June) are significantly lower than in the second two quarters (July&ndash;December) (p < 0.0001). In the Central Valley of California, though not statistically significant (p = 0.4169), arsenic concentration is lower in the first quarter of the year but increases in subsequent quarters. In both regions, these changes appear to follow groundwater levels. It is possible that this difference in arsenic concentrations is related to groundwater level changes, pumping stresses, evapotranspiration effects, or perhaps mixing of more oxidizing, lower pH recharge water in wetter months. Focusing on the understanding the geochemical conditions in aquifers where arsenic concentrations are concerns and causes of geochemical changes in the groundwater environment may lead to a better understanding of where and by how much arsenic will vary over time.

Science of the Total Environment↗

Arsenic, iron, lead, manganese, and uranium concentrations in private bedrock wells in southeastern New Hampshire, 2012-2013

Trace metals, such as arsenic, iron, lead, manganese, and uranium, in groundwater used for drinking have long been a concern because of the potential adverse effects on human health and the aesthetic or nuisance problems that some present. Moderate to high concentrations of the trace metal arsenic have been identified in drinking water from groundwater sources in southeastern New Hampshire, a rapidly growing region of the State (Montgomery and others, 2003). During the past decade (2000–10), southeastern New Hampshire, which is composed of Hillsborough, Rockingham, and Strafford Counties, has grown in population by nearly 48,700 (or 6.4 percent) to 819,100. These three counties contain 62 percent of the State’s population but encompass only about 22 percent of the land area (New Hampshire Office of Energy and Planning, 2011). According to a 2005 water-use study (Hayes and Horn, 2009), about 39 percent of the population in these three counties in southeastern New Hampshire uses private wells as sources of drinking water, and these wells are not required by the State to be routinely tested for trace metals or other contaminants. Some trace metals have associated human-health benchmarks or nonhealth guidelines that have been established by the U.S. Environmental Protection Agency (EPA) to regulate public water supplies. The EPA has established a maximum contaminant level (MCL) of 10 micrograms per liter (μg/L) for arsenic (As) and a MCL of 30 μg/L for uranium (U) because of associated health risks (U.S. Environmental Protection Agency, 2012). Iron (Fe) and manganese (Mn) are essential for human health, but Mn at high doses may have adverse cognitive effects in children (Bouchard and others, 2011; Agency for Toxic Substances and Disease Registry, 2012); therefore, the EPA has issued a lifetime health advisory (LHA) of 300 μg/L for Mn. Recommended secondary maximum contaminant levels (SMCLs) for Fe (300 μg/L) and Mn (50 μg/L) were established primarily as nonhealth guidelines—based on aesthetic considerations, such as taste or the staining of laundry and plumbing fixtures—because these contaminants, at the SMCLs, are not considered to present risks to human health. Because lead (Pb) contamination of drinking water typically results from corrosion of plumbing materials belonging to water-system customers but still poses a risk to human health, the EPA established an action level (AL) of 15 μg/L for Pb instead of an MCL or SMCL (U.S. Environmental Protection Agency, 2012). The 15-μg/L AL for Pb has been adopted by the New Hampshire Department of Environmental Services for public water systems, and if exceeded, the public water system must inform their customers and undertake additional actions to control corrosion in the pipes of the distribution system (New Hampshire Department of Environmental Services, 2013). Unlike the quality of drinking water provided by public water suppliers, the quality of drinking water obtained from private wells in New Hampshire is not regulated; consequently, private wells are sampled only when individual well owners voluntarily choose to sample them. The U.S. Geological Survey (USGS), in cooperation with the EPA New England, conducted an assessment in 2012–13 to provide private well owners and State and Federal health officials with information on the distribution of trace-metal (As, Fe, Pb, Mn, and U) concentrations in groundwater from bedrock aquifers in the three counties of southeastern New Hampshire. This fact sheet analyzes data from water samples collected by a randomly selected group of private well owners from the three-county study area and describes the major findings for trace-metal concentrations.

New Hampshire↗

Heterogeneous redox conditions, arsenic mobility, and groundwater flow in a fractured-rock aquifer near a waste repository site in New Hampshire, USA

Anthropogenic sources of carbon from landfill or waste leachate can promote reductive dissolution of in situ arsenic (As) and enhance the mobility of As in groundwater. Groundwater from residential-supply wells in a fractured crystalline-rock aquifer adjacent to a Superfund site in Raymond, New Hampshire, USA, showed evidence of locally enhanced As mobilization in relatively reducing (mixed oxic-anoxic to anoxic) conditions as determined by redox classification and other lines of evidence. Redox classification was determined from geochemical indicators based on threshold concentrations of dissolved oxygen (DO), nitrate (NO 3- ), iron (Fe 2+ ), manganese (Mn 2+ ), and sulfate (SO 4 2- ). Redox conditions were evaluated also based on methane (CH 4 ), excess nitrogen gas (N 2 ) from denitrification, the oxidation state of dissolved As speciation (As(III) and As(V)), and several stable isotope ratios. Samples from the residential-supply wells primarily exhibit mixed redox conditions, as most have long open boreholes (typically 50&ndash;100 m) that receive water from multiple discrete fractures with contrasting groundwater chemistry and redox conditions. The methods employed in this study can be used at other sites to gauge redox conditions and the potential for As mobilization in complex fractured crystalline-rock aquifers where multiple lines of evidence are likely needed to understand As occurrence, mobility, and transport.

New Hampshire↗

Geophysical and flow-weighted natural-contaminant characterization of three water-supply wells in New Hampshire

Three bedrock water-supply systems in New Hampshire were studied, using borehole geophysics and flow-weighted sampling techniques, to determine the sources and distribution of natural contaminants in water entering the boreholes and to assess whether borehole modifications might be used to reduce contaminant levels. Well water in more than 100 community water-supply systems in New Hampshire have natural contaminants, such as arsenic and uranium, above the U.S. Environmental Protection Agency maximum contaminant levels of 10 and 30 micrograms per liter, respectively. The water-system wells were studied to identify fractional contributions of natural contaminants from specific fracture zones. The yields and flow-weighted contaminant levels of such fracture zones were assessed to determine if a modification of the borehole might lead to a reduction in the system&rsquo;s contaminant levels. The water-supply systems investigated were typical of small community water systems in New Hampshire where a water system may serve 100 connections or less. Each water system consisted of two wells, approximately 300 to 400 feet deep, in generally low-yielding (about 10 gallons per minute or less) crystalline bedrock. The wells were typically operated a few hours per day to fill a storage tank and had tens of feet of drawdown caused by the low well yields. The systems selected had contaminant concentrations slightly above MCL, or a low-level contamination. One of the water systems investigated had low-level (10 to 24 micrograms per liter) arsenic contamination, and two of the water systems had low-level uranium (30 to 40 micrograms per liter) contamination. The contaminant values were blended-water concentrations from the two wells in a system. Each water system had differences in contaminant concentrations between the two wells. In each case, the well with the greater concentration of the two was selected for investigation. In two of the three systems investigated, there was either not enough variation in the borehole contaminant concentration or not enough water-yielding fractures for borehole modifications to be a viable potential remedy to elevated contamination. However, borehole and contaminant conditions in one of the bedrock supply-well systems may be favorable to potential improvement of supplied water by borehole modification where selected fracture zones are sealed off from supplying water to the well.

New Hampshire↗

Continuous-resistivity profiling for coastal ground-water investigations: Three case studies

Continuous-resistivity profiling (CRP) was used at three sites to investigate submarine groundwater discharge (SGD) and to delineate the subsurface saltwater/freshwater interface. At the first site, in Georgetown, South Carolina, CRP was used to locate possible areas of SGD in the Winyah Bay estuary. The data show evidence of SGD in the Pee Dee River, feeding into Winyah Bay, at approximately the location of the forest/marsh boundary. In Waquoit Bay, Massachusetts, CRP was used to further map the extent of SGD already measured by sea floor seepage meters and to delineate the subsurface saltwater/freshwater boundary. The data show evidence for a focused groundwater plume beneath the bay that may extend 350 meters (m) out from the shore. Finally, CRP was used in Orleans, Massachusetts, to verify a groundwater model prediction of freshwater-saturated sediments underlying an area of Cape Cod Bay, just west of Rock Harbor. The data support the prediction of freshwater-saturated sediments beneath the bay. Results from all three sites show the value of CRP in coastal groundwater investigations.

Massachusetts, South Carolina↗

An integrated surface-geophysical investigation of the University of Connecticut landfill, Storrs, Connecticut: 2000

A surface-geophysical investigation to characterize the hydrogeology and contaminant distribution of the former landfill area at the University of Connecticut in Storrs, Connecticut, was conducted in 2000 to supplement the preliminary hydrogeologic assessment of the contamination of soil, surface water, and ground water at the site. A geophysical-toolbox approach was used to characterize the hydrogeology and contaminant distribution of the former landfill. Two-dimensional direct-current resistivity, inductive terrain-conductivity, and seismic-refraction surface-geophysical data were collected and interpreted in an iterative manner with exploratory drilling, borehole geophysics, and hydraulic testing. In this investigation, a geophysical-toolbox approach was used to 1) further define previously identified conductive anomalies and leachate plumes; 2) identify additional leachate plumes, possible fracture zones, and (or) conductive lithologic layers in the bedrock; and 3) delineate bedrock-surface topography in the drainage valleys north and south of the landfill. Resistivity and terrain-conductivity surveys were used to further delineate previously identified geophysical anomalies to the north and southwest of the landfill. A conductive anomaly identified in the terrain-conductivity survey to the north of the landfill in 2000 had a similar location and magnitude as an anomaly identified in terrain-conductivity surveys conducted in 1998 and 1999. Collectively, these surveys indicated that the magnitude of the conductive anomaly decreased with depth and with distance from the landfill. These anomalies indicated landfill leachate in the overburden and shallow bedrock. Results of previous surface-geophysical investigations southwest of the landfill indicated a shallow conductive anomaly in the overburden that extended into the fractured-bedrock aquifer. This conductive anomaly had a sheet-like geometry that had a north-south strike, dipped to the west, and terminated abruptly about 450 feet southwest of the landfill. The sheet-like conductive anomaly was interpreted as a fractured, conductive lithologic feature filled with conductive fluids. To further delineate this anomaly, two two-dimensional resistivity profiles were collected west of the sheet-like conductive anomaly to assess the possibility that the sheet-like conductive anomaly continued to the west in its down-dip direction. Each of the north-south oriented resistivity profiles showed bullet-shaped rather than linear-shaped anomalies, with a relatively smaller magnitude of conductivity than the sheet-like conductive anomaly to the east. If these bullet-like features are spatially connected, they may represent a linear, or pipe-like, conductive anomaly in the bedrock with a trend of N290°E and a plunge of 12°. Additional surveys were conducted to assess the apparent southern termination of the sheet-like conductive feature. Terrain-conductivity surveys indicated the sheet-like feature was not continuous to the south. A two-dimensional resistivity line and a coincident terrain-conductivity profile indicated the presence of a steep, eastward dipping, low magnitude, electrically conductive anomaly on the eastern end of the profile. Although the sheet-like conductive anomaly apparently did not continue to the south, the survey conducted in 2000 identified an isolated, weak conductive anomaly south of the previously identified anomaly. Inductive terrain-conductivity surveys performed north of the sheet-like conductive anomaly and west of the landfill indicated the anomaly did not extend to the north into the area of the former chemical-waste disposal pits. No conductive plumes or conductive features were observed in the subsurface bedrock west of the landfill. A conductive anomaly was identified in the southern section of the new terrain-conductivity grid. The magnitude and distribution of the apparent conductivity of this anomaly was identified as a nearly vertical sheet-like conductive feature. The anomaly extended north-south for 150 feet, and the depth and (or) magnitude of the conductive anomaly decreased towards the south. Based on the location, orientation, and dip, this feature was interpreted as a separate anomaly rather than as a continuation of the sheet-like, conductive bedrock feature that was previously identified southwest of the landfill. No other new conductive anomalies were identified south or west of the landfill. Seismic-refraction surveys were used to delineate the depth to the water table and the depth and topography of the bedrock surface. The seismic-refraction surveys at the northern and southern ends of the landfill confirm the presence of shallow bedrock at 25 feet below land surface. Seismic-refraction surveys conducted southwest of the landfill in a minor topographic valley indicate the bedrock is about 10 feet below land surface.

Connecticut↗

Integrated geophysical characterization of the Winthrop Landfill Southern Flow Path, Winthrop, Maine

The U.S. Geological Survey (USGS), in cooperation with United Technologies Corporation, used an integrated suite of borehole, surface, and water-borne geophysical methods near the site of the former Winthrop Landfill, Winthrop, Maine, to investigate the hydrogeology controlling the transport of leachate from the landfill to nearby Annabessacook Lake. During the fall of 2000 and summer of 2001, the USGS conducted borehole electromagnetic (EM) induction and gamma logging, and inductive terrain-conductivity, two-dimensional (2D) resistivity, continuous seismic reflection, and magnetic surveys. The objectives of this integrated geophysical study were to provide constraints on the location and extent of the southern flow path(s) of contamination from the landfill to the lake; identify shoreline seep geophysical signatures; identify potentially hidden seeps in the lake; and determine depth to bedrock below Annabessacook Lake in the study area. Interpretation of surface 2D resistivity, magnetic, and inductive terrain-conductivity data and borehole EM logs delineates an electrically conductive anomaly consistent with a leachate plume moving from the current landfill boundary southward through the overburden to the shores of Annabessacook Lake. Surface and borehole geophysical data collected south and southeast of the landfill indicate the presence of discrete, shallow conductive anomalies at the southeastern edge of the landfill and near the lakeshore. The conductive anomalies appear at increasing depths closer to the lake. Magnetic anomalies offshore confirm the presence of iron-rich landfill leachate discharging into the lake south of the landfill. High-resolution swept-frequency seismic data used to map sediment and grain size distribution in the lake sub-bottom along the shoreline identified sediment-infilled bedrock lows that may act as conduits for contaminant migration.

Maine↗