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R.T. Kay

Publications and source records attributed to R.T. Kay.

3 recordsLinked to original sources

Concentrations of polycyclic aromatic hydrocarbons and inorganic constituents in ambient surface soils, Chicago, Illinois: 2001-2002

Samples of ambient surface soils were collected from 56 locations in Chicago, Illinois, using stratified random sampling techniques and analyzed for polycyclic aromatic hydrocarbon (PAH) compounds and inorganic constituents. PAHs appear to be derived primarily from combustion of fossil fuels and may be affected by proximity to industrial operations, but do not appear to be substantially affected by the organic carbon content of the soil, proximity to nonindustrial land uses, or proximity to a roadway. Atmospheric settling of particulate matter appears to be an important mechanism for the placement of PAH compounds into soils. Concentrations of most inorganic constituents are affected primarily by soil-forming processes. Concentrations of lead, arsenic, mercury, calcium, magnesium, phosphorus, copper, molybdenum, zinc, and selenium are elevated in ambient surface soils in Chicago in comparison to the surrounding area, indicating anthropogenic sources for these elements in Chicago soils. Concentrations of calcium and magnesium in Chicago soils appear to reflect the influence of the carbonate bedrock parent material on the chemical composition of the soil, although the effects of concrete and road fill cannot be discounted. Concentrations of inorganic constituents appear to be largely unaffected by the type of nearby land use. Copyright ?? Taylor & Francis Group, LLC.

Soil and Sediment Contamination

Potentiometric levels and water quality in the aquifers underlying Belvidere, Illinois, 1993–96

In 1992, the U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency (USEPA), began a study of the hydrogeology and water quality of the aquifers underlying the vicinity of Belvidere, Boone County, Ill. Previously, volatile organic compounds (VOC's) and other constituents of industrial origin were detected in one or more ground-water samples from about 100 of the approximately 700 monitoring and water-supply wells in the area, including the 8 municipal wells in Belvidere. A glacial drift aquifer underlies at least 50 percent of the 80-square-mile study area; bedrock aquifers that underlie virtually all of the study area include the Galena-Platteville, St. Peter Sandstone, Ordovician, and Cambrian-Ordovician aquifers. During 1993, water levels were measured in 152 wells and water-quality samples were collected from 97 wells distributed throughout the study area. During 1994–96, similar data were collected from 31 wells. Potentiometric levels in the glacial drift and Galena-Platteville aquifers are similar and range from about 750 to 900 feet above sea level. The potentiometric surfaces of the aquifers are subdued representations of the land surface. Horizontal ground-water flow in the aquifers primarily is towards the Kishwaukee River, which flows through the central part of the study area, and its principal tributaries. Vertical ground-water flow appears to be downward at most locations in the study area, particularly in the urbanized areas affected by pumping of the Belvidere municipal wells and upland areas remote from the principal surface-water drainages. Flow appears to be upward between the Galena-Platteville and glacial drift aquifers where ground water discharges to the Kishwaukee River and its principal tributaries. All water samples were analyzed for VOC's. Selected samples also were analyzed for trace metals, cyanide, semivolatile organic compounds, or other constituents. VOC's were detected in samples from 50 wells (52 percent of total wells sampled). Twenty-seven specific VOC's were identified in the samples. Samples were collected from six municipal wells in use during the study; two wells were not in use because one or more VOC's exceeded maximum contaminant levels (MCL's). Two VOC's were detected in one of the samples at concentrations below MCL's established by the USEPA for protection of public-water supplies. Samples from 21 wells had at least one VOC detected at a concentration above MCL's. The VOC's detected above MCL's and their maximum concentrations were 1,2-dichloroethene (total), 470 micrograms per liter; trichloroethene (TCE), 360 micrograms per liter; tetrachloroethene (PCE), 82 micrograms per liter; benzene, 53 micrograms per liter; and vinyl chloride, 11 micrograms per liter. TCE and PCE were the most frequently detected VOC's and generally had the highest concentrations. VOC's with concentrations above MCL's were detected in samples from 15 wells open to the glacial drift aquifer and 6 wells open to the Galena-Platteville aquifer. Generally, the concentrations of VOC's were higher, and number and type of VOC's detected were greater in the glacial drift aquifer than in the Galena-Platteville aquifer and the deeper bedrock aquifers. The high concentrations and spatial distribution of VOC's in the glacial drift aquifer usually were related to nearby sources of contamination. Except in the immediate vicinity of a known hazardous-waste site, possible sources of VOC's in the bedrock aquifers were difficult to identify in the study area; VOC concentrations at most locations in the bedrock aquifers were below 5 micrograms per liter. Most locations where VOC's were detected in the glacial and bedrock aquifers were within about 1,000 feet of the Kishwaukee River. Hydrogeologic factors that affect the distribution of VOC's in the aquifers include ground-water flow through (1) the glacial drift aquifer with discharge to the nearby Kishwaukee River; and (2) the weathered-surface deposits, bedding-plane partings, and fractures in the Galena-Platteville aquifer. One bedding-plane parting intersecting wells that represent an area of about 1.5 square miles has a horizontal hydraulic conductivity as high as 220 feet per day. Pumping of high-capacity wells may contribute to the widespread distribution of VOC’s at low concentrations in the bedrock aquifers.

Illinois

Geohydrology and ground-water quality in the vicinity of a ground-water-contamination site in Rockford, Illinois

A geohydrologic investigation was performed by the U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, to determine the distribution of volatile organic compounds in a fractured-rock aquifer near the Southeast Rockford Groundwater Contamination Site in Rockford, Ill. The geologic units of concern are the St. Peter Sandstone and Glenwood Formation; the dolomites of the Platteville and Galena Groups of Ordovician age; and the sands, gravels, silts, and clays of Quaternary age. The hydraulic units of concern are the unconsolidated aquifer, composed of sand and gravel; the fractured- dolomite aquifer, composed of the Galena and Platteville Groups and the dolomitic sections of the Glenwood Formation; and the sandstone aquifer, composed of the St. Peter Sandstone and the sandstone beds in the Glenwood Formation. The dolomite aquifer is well connected hydraulically to the overlying unconsolidated aquifer and the underlying sandstone aquifer. Caliper and acoustic-televiewer logs show several subhorizontal fractures in the dolomite that can be correlated throughout the study area. Comparison of televiewer and flowmeter logs indicates that most of the flow in the dolomite aquifer is through these fractures. Ground-water flow through two of the fractures can be correlated over large parts of the study area. Volatile organic compounds, in concentrations exceeding 2,000 micrograms per liter, were detected within the entire thickness of the dolomite aquifer where flow is measurable. Volatile organic compounds were detected in an area of the aquifer where they were thought to be absent in previous investigations.

Illinois