Search USGSSearch

Geology topics

Sheridan K. Haack

Publications and source records attributed to Sheridan K. Haack.

25 records · Page 2Linked to original sources

Arsenic in ground water in Livingston County, Michigan

Previous studies of ground-water resources in Michigan by the Michigan Department of Community Health (MDCH), the Michigan Department of Environmental Quality (MDEQ), and the U.S. Geological Survey (USGS) indicate that in several counties in the southeastern part of the State the concentrations of arsenic in ground water may exceed the U.S. Environmental Protection Agency (USEPA) maximum contaminant level (MCL) of 50 micrograms per liter [µg/L]. This MCL was established in 1986. The Safe Drinking Water Act, as amended in 1996, requires USEPA to revise this standard in 2000. In June 2000, the USEPA proposed a revised MCL of 5 µg/L. In 1996, the USGS, in cooperation with the MDEQ and the Health Departments of Genesee, Huron, Lapeer, Livingston, Oakland, Sanilac, Shiawassee, Tuscola and Washtenaw counties, began a study of the factors controlling arsenic occurrence and concentrations in ground water in southeastern Michigan. This study is one of four USGS Drinking Water Initiative projects throughout the United States.

Michigan

Arsenic in ground water in Shiawassee County, Michigan

Previous studies of ground-water resources in Michigan by the Michigan Department of Community Health (MDCH), the Michigan Department of Environmental Quality (MDEQ), and the U.S. Geological Survey (USGS) indicate that in several counties in the southeastern part of the State the concentrations of arsenic in ground water may exceed the U.S. Environmental Protection Agency (USEPA) maximum contaminant level (MCL) of 50 micrograms per liter [µg/L]. This MCL was established in 1986. The Safe Drinking Water Act, as amended in 1996, requires USEPA to revise this standard in 2000. In June 2000, the USEPA proposed a revised MCL of 5 µg/L. In 1996, the USGS, in cooperation with the MDEQ and the Health Departments of Genesee, Huron, Lapeer, Livingston, Oakland, Sanilac, Shiawassee, Tuscola and Washtenaw counties, began a study of the factors controlling arsenic occurrence and concentrations in ground water in southeastern Michigan. This study is one of four USGS Drinking Water Initiative projects throughout the United States.

Michigan

Arsenic in ground water in Sanilac County, Michigan

Previous studies of ground-water resources in Michigan by the Michigan Department of Community Health (MDCH), the Michigan Department of Environmental Quality (MDEQ), and the U.S. Geological Survey (USGS) indicate that in several counties in the southeastern part of the State the concentrations of arsenic in ground water may exceed the U.S. Environmental Protection Agency (USEPA) maximum contaminant level (MCL) of 50 micrograms per liter [µg/L]. This MCL was established in 1986. The Safe Drinking Water Act, as amended in 1996, requires USEPA to revise this standard in 2000. In June 2000, the USEPA proposed a revised MCL of 5 µg/L. In 1996, the USGS, in cooperation with the MDEQ and the Health Departments of Genesee, Huron, Lapeer, Livingston, Oakland, Sanilac, Shiawassee, Tuscola and Washtenaw counties, began a study of the factors controlling arsenic occurrence and concentrations in ground water in southeastern Michigan. This study is one of four USGS Drinking Water Initiative projects throughout the United States.

Michigan

Arsenic in ground water in Tuscola County, Michigan

Previous studies of ground-water resources in Michigan by the Michigan Department of Community Health (MDCH), the Michigan Department of Environmental Quality (MDEQ), and the U.S. Geological Survey (USGS) indicate that in several counties in the southeastern part of the State the concentrations of arsenic in ground water may exceed the U.S. Environmental Protection Agency (USEPA) maximum contaminant level (MCL) of 50 micrograms per liter [µg/L]. This MCL was established in 1986. The Safe Drinking Water Act, as amended in 1996, requires USEPA to revise this standard in 2000. In June 2000, the USEPA proposed a revised MCL of 5 µg/L. In 1996, the USGS, in cooperation with the MDEQ and the Health Departments of Genesee, Huron, Lapeer, Livingston, Oakland, Sanilac, Shiawassee, Tuscola and Washtenaw counties, began a study of the factors controlling arsenic occurrence and concentrations in ground water in southeastern Michigan. This study is one of four USGS Drinking Water Initiative projects throughout the United States.

Michigan

Arsenic in ground water in Washtenaw County, Michigan

Previous studies of ground-water resources in Michigan by the Michigan Department of Community Health (MDCH), the Michigan Department of Environmental Quality (MDEQ), and the U.S. Geological Survey (USGS) indicate that in several counties in the southeastern part of the State the concentrations of arsenic in ground water may exceed the U.S. Environmental Protection Agency (USEPA) maximum contaminant level (MCL) of 50 micrograms per liter [µg/L]. This MCL was established in 1986. The Safe Drinking Water Act, as amended in 1996, requires USEPA to revise this standard in 2000. In June 2000, the USEPA proposed a revised MCL of 5 µg/L. In 1996, the USGS, in cooperation with the MDEQ and the Health Departments of Genesee, Huron, Lapeer, Livingston, Oakland, Sanilac, Shiawassee, Tuscola and Washtenaw counties, began a study of the factors controlling arsenic occurrence and concentrations in ground water in southeastern Michigan. This study is one of four USGS Drinking Water Initiative projects throughout the United States.

Michigan

Arsenic concentration and selected geochemical characteristics for ground water and aquifer materials in southeastern Michigan

Fifty-six private wells, 20 public wells and 38 monitoring wells in ten counties in southeastern Michigan were sampled to determine the concentration of naturally-occurring arsenic and specific geochemical parameters. The majority of ground water samples were analyzed for pH, dissolved oxygen, oxidation/reduction potential, specific conductance, major ions, dissolved and suspended organic carbon, and arsenic. Selected samples were analyzed for minor elements, nutrients, the isotope ratio of carbon and the concentration of tritium. The Mississippian Marshall Sandstone comprises a major aquifer in southeastern Michigan. To compare the lithology of the Marshall Aquifer to water chemistry, two new wells were drilled through the Marshall Sandstone to the underlying Coldwater Shale. Depth-specific bedrock and water samples were collected from these wells. For public and private drinking-water wells, the lowest concentration detected by USGS analysis was <1 microgram per liter and the highest was 220 micrograms per liter. Arsenic concentrations near or exceeding the current USEPA standard of 50 micrograms per liter occurred in ground water from each of the major aquifers in the study area. In the two newly-drilled wells, the lowest concentration detected by the USGS was <1 microgram per liter at about 350 ft below land surface and the highest concentration of 140 micrograms per liter was detected at around 50 ft below land surface. The data from this study may be used to indicate well characteristics and water chemistry factors that are related to arsenic in ground water in southeastern Michigan.

Michigan

Comparison of Eh and H2 measurements for delineating redox processes in a contaminated aquifer

Measurements of oxidation-reduction potential ( E h ) and concentrations of dissolved hydrogen (H 2 ) were made in a shallow groundwater system contaminated with solvents and jet fuel to delineate the zonation of redox processes. E h measurements ranged from +69 to -158 mV in a cross section of the contaminated plume and accurately delineated oxic from anoxic groundwater. Plotting measured E h and pH values on an equilibrium stability diagram indicated that Fe(III) reduction was the predominant redox process in the anoxic zone and did not indicate the presence of methanogenesis and sulfate reduction. In contrast, measurements of H 2 concentrations indicated that methanogenesis predominated in heavily contaminated sediments near the water table surface (H 2 ∼ 7.0 nM) and that the methanogenic zone was surrounded by distinct sulfate-reducing (H 2 ∼ 1-4 nM) and Fe(III)-reducing (H 2 ∼ 0.1-0.8 nM) zones. The presence of methanogenesis, sulfate reduction, and Fe(III) reduction was confirmed by the distribution of dissolved oxygen, sulfate, Fe(II), and methane in groundwater. These results show that H 2 concentrations were more useful for identifying anoxic redox processes than E h measurements in this groundwater system. However, H 2 -based redox zone delineations are more reliable when H 2 concentrations are interpreted in the context of electron-acceptor (oxygen, nitrate, sulfate) availability and the presence of final products [Fe(II), sulfide, methane] of microbial metabolism.

Environmental Science & Technology