Geology Reports⌕ Search

Geology topics

J.T. De Roche

Publications and source records attributed to J.T. De Roche.

6 recordsLinked to original sources

Hydrogeology, simulated ground-water flow, and ground-water quality, Wright-Patterson Air Force Base, Ohio

Ground water is the primary source of water in the Wright-Patterson Air Force Base area. The aquifer consists of glacial sands and gravels that fill a buried bedrock-valley system. Consolidated rocks in the area consist of poorly permeable Ordovician shale of the Richmondian stage, in the upland areas, the Brassfield Limestone of Silurian age. The valleys are filled with glacial sediments of Wisconsinan age consisting of clay-rich tills and coarse-grained outwash deposits. Estimates of hydraulic conductivity of the shales based on results of displacement/recovery tests range from 0.0016 to 12 feet per day; estimates for the glacial sediments range from less than 1 foot per day to more than 1,000 feet per day. Ground water flow from the uplands towards the valleys and the major rivers in the region, the Great Miami and the Mad Rivers. Hydraulic-head data indicate that ground water flows between the bedrock and unconsolidated deposits. Data from a gain/loss study of the Mad River System and hydrographs from nearby wells reveal that the reach of the river next to Wright-Patterson Air Force Base is a ground-water discharge area. A steady-state, three-dimensional ground-water-flow model was developed to simulate ground-water flow in the region. The model contains three layers and encompasses about 100 square miles centered on Wright-Patterson Air Force Base. Ground water enters the modeled area primarily by river leakage and underflow at the model boundary. Ground water exits the modeled area primarily by flow through the valleys at the model boundaries and through production wells. A model sensitivity analysis involving systematic changes in values of hydrologic parameters in the model indicates that the model is most sensitive to decreases in riverbed conductance and vertical conductance between the upper two layers. The analysis also indicates that the contribution of water to the buried-valley aquifer from the bedrock that forms the valley walls is about 2 to 4 percent of the total ground-water flow in the study area. Ground waters in the vicinity of Wright-Patterson Air Force Base can be classified into two compositional groups on the basis of their chemical composition: calcium magnesium bicarbonate-type and sodium chloride-type waters. Calcium magnesium bicarbonate-type waters are found in the glacial deposits and the Brassfield Limestone, whereas the sodium chloride waters are exclusively associated with the shales. Equilibrium speciation calculations indicate that ground water of the glacial drift aquifer is in equilibrium with calcite, dolomite, and chalcedony, but is undersaturated with respect to gypsum and fluorite. Waters from the shales are slightly supersaturated with respect to calcite, dolomite, and siderite but are undersaturated with respect to chalcedony. Simple-mass balance calculations treating boron as a conservative species indicate that little (< 5 percent) or no recharge from the shales to the glacial drift aquifer takes place. Data on the stable isotopes of oxygen and hydrogen indicate a meteoric origin for all ground water beneath Wright-Patterson Air Force Base, but the data were inconclusive with respect to identification of distinct isotopic differences between water collected from the glacial drift and bedrock aquifers. Tritium concentrations used to distinguish waters having a pre-and post-1953 recharge component indicate that most water entered the glacial drift aquifer after 1953. This finding indicates that recharge from shallow to deep parts (greater than 150 feet) of the aquifer takes place over time intervals of a few years or decades. However, the fact that some deep parts of the glacial aquifer did not contain measurable tritium indicates that ground-water flow from recharge zones to these parts of the aquifer takes decades or longer.

Water-Resources Investigations Report↗

Hydrogeology and water quality near a solid- and hazardous-waste landfill, Northwood, Ohio

Hydrogeology and water quality of ground water and selected streams were evaluated near a landfill in northwestern Ohio. The landfill is used for codisposal of solid and hazardous waste. Water-level and geologic data were collected from 36 wells and 3 surface-water sites during the period November 1983 to November 1985. Water-quality samples were collected from 18 wells and 3 surface-water sites this during this same period. The primary aquifers in the area are the Greenfield Dolomite and underlying Lockport Dolomite of Silurian age. These bedrock carbonates are overlain by two clay tills of Wisconsin age. The tills are capped by a glacial lake clay. The tills generally are saturated, but do not yield sufficient water to be considered an aquifer. Two wells in the study area yield water, in part, from discontinuous deposits of outwash sand and gravel at the lower till-bedrock interface. Regional ground-water flow is from southwest to northeast; local flow is influenced by a ground-water mound centered under the northernmost cells of the landfill. Water levels in wells penetrating refuse within the landfill and the presence of leachate seeps indicate that the refuse is saturated. Head relations among the landfill, till, and dolomite aquifer indicate a vertical component of flow downward from the landfill to the dolomite aquifer. Water levels near the landfill fluctuate as much as 14 feet per year, in contrast to fluctuations of less than 3 feet per year in wells upgradient landfill. Ground waters from wells completed in the dolomite aquifer and glacial till were found to have major-iron concentrations controlled, in large part, by reaction with calcite, dolomite, and other minerals in the aquifer. Only minor departures from equilibrium mineral saturation were noted for ground water, except in wells affected by cement/grout contamination. Molal ratios of calcuim:magnesium in ground water suggest a similar chemical evolution of waters throughout the dolomite aquifer in the study area. Stable-isotope ratios of oxygen and hydrogen indicate the source of water in the till unit and dolomite aquifer is atmospheric precipitation. Elevated levels of total dissolved solids, boron, ammonia, and iron in the leachate and in wells downgradient of the landfill may indicate mixing of ground water with leachate. Oxygen and hydrogen stable-isotope ratios were used to differentiate waters from the glacial till and dolomite aquifer. Isotope ratios also show a shift off the local mixing line for leachate and for a well just downgradient from the landfill. The shift to heavier values of o D in the well water may be indicative of leachate mixing with ground water. The effect of this mixing denoted by hydrologic, isotopic, and chemical-quality data is limited mostly to elevated levels of the common ions. Analysis did not indicate significant levels of toxic metals or organic contaminants except phenol, which was present at concentrations of from 1 to 5 micrograms per liter in six wells. Analysis of water-quality data from nearby streams suggest that surface leaching from the landfill does not significantly affect stream-water quality, but may contribute to higher level of trace metals in the streambed sediments.

Water-Resources Investigations Report↗

Hydrogeology and effects of landfills on ground-water quality, southern Franklin County, Ohio

Hydrogeology and water quality were evaluated near five land-fills along a 5-mile segment of the Scioto River valley south of Columbus, Ohio. Heterogenous surficial deposits o sand, gravel, and till up to 160 feet thick are hydraulically connected to the underlying Devonian limestone, the landfills and Scioto River, which has been leveed with 12 to 35 feet of refuse. Ground-water withdrawals caused a maximum 21-foot decline in ground-water levels from 1979 to 1982. The study reach of Scioto River within the influence of ground-water pumping is a losing stream, except for s small segment adjacent to one landfill. Analysis of variance indicated significant difference in ground-water quality between wells upgradient of landfills, down-gradient of landfills, and wells penetrating refuse. Elevated specific conductance and concentrations of total dissolved solids, ammonia, carbon dioxide, and dissolved organic carbon in water from wells downgradient from and penetrating landfills indicate leachate production and migration is occurring. Analysis of bed-material samples from Scioto River and Scioto Big Run revealed concentrations of polynuclear aromatic hydrocarbons ranging from 220 to 9,440 micograms per kilogram of sediment (?g/kg) and concentrations of toxic metals ranging from 1 to 720 ?g/kg. Samples from an upstream control station on Scioto River contained no organic compounds and lower concentrations of metals (ranging from 1 to 260 ?g/kg). Because of multiple land uses within the study area, organic compounds recovered from the streamed sediments cannot be attributed to any single source. The generation of hydrogen sulfide and methane gases, presence of a zone of increased hardness, elevated concentrations of common ionic species, and dominance of ammonia over other nitrogen species indicate that leachate is being produced and its migrating from four landfills and the river levee. Based on hydraulic relationships between ground water and surface water, it is highly probable that ground water contaminated by leachate from the levee and from one of the landfills is discharging to Scioto River. Leachate-enriched groundwater from other landfills also may begin to discharge to the river if water-withdrawal patterns in the study area change.

Water-Resources Investigations Report↗

Water quality of a stream-aquifer system, southern Franklin County, Ohio

The chemical quality of the water resources in the Scioto River valley south of Columbus, Ohio, was evaluated on the basis of data collected from 74 wells and 4 surface-water sites. A very hard calcium bicarbonate water that is high in dissolved solids is characteristic of the aquifer. Mean pH of the ground water is 7.3, and bicaerbonate concentrations range from 238 to 530 milligrams per liter. Concentrations of dissolved iron in water samples (0.01 to 3.9 milligrams per liter) frequently exceed the drinking water standard of 0.3 milligrams per liter established by the Ohio Environmental Protection Agency. The chemical quality of local streams closely resembles the ground-water quality, except for higher concentrations of sodium, chloride, and sulfate in the surface water. Microbiological testing of ground water for fecal bacteria indicated concentrations ranging from 1 to 2,400 colonies per 100 milliliters. The higher concentrations were observed in one well on the Scioto River flood plain after a flood event. Mass-balance calculations of the chemical data indicate that pH is buffered primarily by the carbonate system. Data for pH, calculated Eh, and concentrations of ferrous iron and reduced sulfur show that areas of different chemical environments exist within the aquifer. A reaction model of an induced-infiltration radial collector system indicates the amount of mass transfer (chemical reactions that occur as ground water and surface water mix) is small, and that the mixing ratio between ground and surface waters is four to one.

Water-Resources Investigations Report↗

Ground-water quality in the vicinity of landfill sites, southern Franklin County, Ohio

The hydrogeology and ground-water quality in the vicinity of five landfills in southern Franklin County, Ohio, were investigated by use of data obtained from 46 existing wells, 1 seep, 1 surface-water site, and 1 leachate-collection site. Interpretation was based on data from the wells, a potentiometric-surface map, and chemical analyses. Four of the five landfills are in abandoned sand and gravel pits. Pumping of water from a quarry near the landfills has modified the local ground-water flow pattern, increased the hydraulic gradient, and lowered the water table. Ground water unaffected by the landfills is a hard, calcium bicarbonate type with concentrations of dissolved iron and dissolved sulfate as great as 3.0 milligrams per liter and 200 milligrams per liter, respectively. Water sampled from wells downgradient from two landfills shows an increase in sodium, chloride, and other constituents. The change in water quality cannot be traced directly to the landfills, however, because of well location and the presence of other potential sources of contamination. Chemical analysis of leachate from a collection unit at one landfill shows significant amounts of zinc, chromium, copper, and nickel, in addition to high total organic carbon, biochemical oxygen demand, and organic nitrogen. Concentrations of chloride, iron, lead, manganese and phenolic compounds exceed Ohio Environmental Protection Agency Water Quality Standards for drinking water. Water from unaffected wells within the study area have relatively small amounts of these constituents. (USGS)

Open-File Report↗