Search USGS⌕ Search

Geology topics

Stephanie Dunkle Shapiro

Publications and source records attributed to Stephanie Dunkle Shapiro.

7 recordsLinked to original sources
USGS2006

The chemical quality of self-supplied domestic well water in the United States

Existing water quality data collected from domestic wells were summarized to develop the first national‐scale retrospective of self‐supplied drinking water sources. The contaminants evaluated represent a range of inorganic and organic compounds, and although the data set was not originally designed to be a statistical representation of national occurrence, it encompasses large parts of the United States including at least some wells sampled in every state and Puerto Rico. Inorganic contaminants were detected in many of the wells, and concentrations exceeded the U.S. EPA maximum contaminant levels (MCLs; federal drinking water standards used to regulate public drinking water quality) more often than organic contaminants. Of the inorganic constituents evaluated, arsenic concentrations exceeded the MCL (10 μg/L) in ∼11% of the 7580 wells evaluated, nitrate exceeded the MCL (10 mg/L) in ∼8% of the 3465 wells evaluated, uranium‐238 exceeded the MCL (30 μg/L) in ∼4% of the wells, and radon‐222 exceeded 300 and 4000 pCi/L (potential drinking water standards currently under review by the U.S. EPA) in ∼75% and 9% of the wells, respectively. The MCLs for total mercury and fluoride were each exceeded in <1% of the wells evaluated. The MCL was exceeded in <1% of all wells for all anthropogenically derived organic contaminants evaluated and was not exceeded for many contaminants. In addition, 10 contaminants evaluated do not currently have an MCL. Atrazine, however, was detected in 24% of the wells evaluated and was the most frequently detected organic contaminant of the 28 organic contaminants evaluated in this study. Simazine and metolachlor each were detected in ∼9% of all wells and tied for second in frequency of detection for organic contaminants. The third and fourth most frequently detected organic contaminants were methyl tert ‐butyl ether (MTBE) (6%) and chloroform (5%), respectively. Because the water quality of domestic wells is not federally regulated or nationally monitored, this study provides a unique, previously nonexistent, perspective on the quality of the self‐supplied drinking water resources used by ∼45 million Americans in the United States.

Ground Water Monitoring and Remediation↗
USGS2005

The stability of chlorofluorocarbons (CFCs) in ground-water samples archived in borosilicate ampoules

The U.S. Geological Survey (USGS) Chlorofluorocarbon (CFC) Laboratory in Reston, Va., has been measuring concentrations of CFCs in ground-water samples since 1989 to estimate the year that a water sample was recharged to a ground-water flow system. The water samples have been collected in flame-sealed borosilicate ampoules. Typically for each site, three samples were analyzed within days to a few months after collection, and additional samples were archived for extended periods of time (up to four years). The stability of CFC concentrations in the archived water samples from the USGS CFC Laboratory was investigated by analyzing the CFC concentrations in archived water samples and comparing them with the CFC concentrations that were obtained soon after the samples were collected. The archived samples selected for analysis were chosen from sites with a wide variety of hydrogeologic and geochemical conditions. For CFC-11 and CFC-12 concentrations, approximately 14% and 10.5%, respectively, of the archived samples were statistically different (both higher and lower) from the concentrations obtained from analyses conducted soon after the sample collection. Most of the extraneous values were attributed to natural variability of CFC concentrations originally in the water discharged from wells, rather than to microbial degradation within the ampoule on storage.

Virginia↗
USGS1999

Use of environmental tracers to evaluate ground-water age and water-quality trends in a buried-valley aquifer, Dayton area, southwestern Ohio

Chlorofluorocarbons (CFC method) and tritium and helium isotopes (3H-3He method) were used as environmental tracers to estimate ground-water age in conjunction with efforts to develop a regional ground-water flow model of the buried-valley aquifer in the Dayton area, southwestern Ohio. This report describes results of CFC and water-quality sampling, summarizes relevant aspects of previously published work, and describes the use of 3H-3He ages to characterize temporal trends in ground-water quality of the buried-valley aquifer near Dayton, Ohio. Results of CFC sampling indicate that approximately 25 percent of the 137 sampled wells were contaminated with excess CFC's that rendered the ground water unsuitable for age dating. Evaluation of CFC ages obtained for the remaining samples indicated that the CFC compounds used for dating were being affected by microbial degradation. The degradation occurred under anoxic conditions that are found in most parts of the buried-valley aquifer. As a result, ground-water ages derived by the CFC method were too old and were inconsistent with measured tritium concentrations and independently derived 3H-3He ages. Limited data indicate that dissolved methane may play an important role in the degradation of the CFC's. In contrast, the 3H-3He technique was found to yield ground-water ages that were chemically and hydrologically reasonable. Ground-water ages derived by the 3H-3He technique were compared to values for selected water- quality characteristics to evaluate temporal trends in ground-water quality in the buried- valley aquifer. Distinct temporal trends were not identified for pH, alkalinity, or calcium and magnesium because of rapid equilibration of ground-water with calcite and dolomite in aquifer sediments. Temporal trends in which the amount of scatter and the number of outlier concentrations increased as ground-water age decreased were noted for sodium, potassium, boron, bromide, chloride, ammonia, nitrate, phosphate, sulfate, and organic carbon. Elevated concentrations of these constituents in shallow ground water are probably related to human activities. Temporal trends in which concentrations declined as ground-water age increased may reflect natural processes that reduce constituent concentrations to low levels. For example, the absence of nitrate detections in ground water recharged before 1980 may indicate natural removal of nitrate by bacterially mediated denitrification. Temporal trends observed for dissolved oxygen, iron, nitrate and silica indicate that these constituents may help identify recently (post-1990) recharged ground water.

Ohio↗
USGS1998

Tritium-helium 3 dating under complex conditions in hydraulically stressed areas of a buried-valley aquifer

The 3 H- 3 He dating method is applied in a buried-valley aquifer near Dayton, Ohio. The study area is large, not all sampling locations lie along well-defined flow paths, and existing wells with variable screen lengths and diameters are used. Reliable use of the method at this site requires addressing several complications: (1) The flow system is disturbed because of high pumping rates and induced infiltration; (2) tritium contamination is present in several areas of the aquifer; and (3) radiogenic helium concentrations are elevated in a significant number of the wells. The 3 H- 3 He ages are examined for self-consistency by comparing the reconstructed tritium evolution to the annual weighted tritium measured in precipitation; deviations result from dispersion, tritium contamination, and mixing. 3 H- 3 He ages are next examined for consistency with chlorofluorocarbon ages; the agreement is poor because of degradation of CFCs. Finally, the 3 H- 3 He ages are examined for consistency with the current understanding of local hydrologic processes; the ages are generally supported by hydrogeologic data and the results of groundwater flow modeling coupled with particle-tracking analyses.

Ohio↗