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Municipal ground-water development and withdrawals in the central Lower Peninsula of Michigan, 1870-1987

Municipal water-supply systems in the central Lower Peninsula of Michigan were categorized into four regions on the basis of source of water for 1987. These categories included water systems that obtained water from aquifers in glacial drift, bedrock, or both, as well as those that obtained water from surface-water sources. Data on ground-water development were collected for 182 municipal water-supply systems for the period 1870-1987. Of the 182 systems, 135 used ground water for supply. Wells in glacial-drift aquifers supplied water for 60 municipalities; wells in bedrock aquifers supplied 58 municipalities. Combinations of wells in bedrock and glacial-drift aquifers supplied 17 municipalities. Surface-water sources supplied 45 municipalities; two municipalities used surface water and ground water. Of the 182 municipal systems, withdrawal data were available for only 145. Withdrawal data were collected for the period 1903-1985. Analysis of annual ground-water withdrawal data for the 145 municipal water-supply systems indicates that average annual per capita municipal ground-water withdrawal ranged from 60 gallons per day per person in 1915 to 166 gallons per day per person in 1973. The maximum reported groundwater withdrawal for the area was 103 million gallons per day in 1979. Records from most municipalities include long periods for which no ground-water withdrawal data are available. The average annual per capita data among the municipalities varies over the period of record because of incomplete reporting of pumping rates, unusually high pumping rates, short-term economic changes, and other changes not associated with local population changes.

Michigan↗

Selected ground-water information for the Columbia Plateau Regional Aquifer System, Washington and Oregon, 1982-1985; Volume I. Geohydrology

This data report presents groundwater information collected and analyzed as part of the U.S. Geological Survey 's Columbia Plateau Regional Aquifer System Analysis study. The information was gathered from July 1982 through September 1985 in the part of the aquifer system in central and eastern Washington, and north-central and eastern Oregon. The report consists of three volumes: volume I, geohydrology; volume II, water levels; and volume III, groundwater quality. (See also W89-02573) (USGS)

Open-File Report↗

Hydrogeology and ground-water quality of the northern part of the Town of Oyster Bay, Nassau County, New York, in 1980

This report presents geohydrologic and water quality data from the northern part of the Town of Oyster Bay, in the north-shore area of Long Island. The groundwater reservoir underlying the area consists of clay, silt, sand, and gravel layers that form six geohydrologic units; from bottom to top: the Lloyd aquifer, Raritan clay, Magothy aquifer, Port Washington aquifer, Port Washington confining unit, and the upper glacial aquifer. Crystalline bedrock underlies the Lloyd aquifer and forms the base of the groundwater system. The regional drought of 1962-67 caused groundwater levels to decline as much as 16 feet, but the water table altitude in 1980 equaled or exceeded predrought levels. Water levels measured in wells screened in the lower part of the Magothy aquifer and in the Lloyd aquifer throughout much of the area are still below those measured before the drought but are recovering. Groundwater in some areas contains nitrates, volatile organic compounds, and chloride in concentrations that exceed New York State drinking-water standards. Contamination is limited largely to the upper glacial aquifer and upper part of the Magothy aquifer. Saltwater has been reported in some wells along the shore but probably represents a natural condition rather than saltwater encroachment due to excessive pumping. (Author 's abstract)

Water-Resources Investigations Report↗

Water-quality assessment of the Rio Grande Valley, Colorado, New Mexico, and Texas: Shallow ground-water quality of a land-use area in the San Luis Valley, south-central Colorado, 1993

This report describes the quality of shallow ground water in an agricultural area in the San Luis Valley, Colorado, and discusses how natural and human factors affect the quality of shallow ground water. Thirty-five wells were installed, and water samples were collected from these wells and analyzed for selected dissolved common constituents, nutrients, trace elements, radionuclides, and synthetic organic compounds. The San Luis Valley is a high intermontane valley that is partially drained by the Rio Grande. The San Luis Valley land-use study area was limited to a part of the valley where the depth to water is generally less than 25 feet. The area where the 35 monitor wells were installed was further limited to the part of the study area where center-pivot overhead sprinklers are used to irrigate crops. Precipitation, runoff from adjacent mountainous areas, and ground-water inflow from the adjacent mountainous areas are the main sources of water to the aquifers in the San Luis Valley. Discharge of water from the shallow, unconfined aquifer in the valley is mainly from evapotranspiration. The dominant land use in the San Luis Valley is agriculture, although nonirrigated land and residential land are interspersed with agricultural land. Alfalfa, native hay, barley, wheat, potatoes, and other vegetables are the main crops. Dissolved-solids concentrations in shallow ground water sampled ranged from 75 to 1,960 milligrams per liter. The largest median concentration of cations was for calcium, and the largest median concentration of anions was for bicarbonate in shallow ground water in the San Luis Valley. Calcium concentrations ranged from 7.5 to 300 milligrams per liter, and bicarbonate concentrations ranged from 28 to 451 milligrams per liter. Nitrite plus nitrate concentrations ranged from less than 0.1 to 58 milligrams per liter as N; water from 11 wells had nitrite plus nitrate concentrations greater than 10 milligrams per liter as N. With the exception of the following trace elements--aluminum, barium, iron, manganese, molybdenum, and uranium--the concentrations of trace elements were less than 10 micrograms per liter in 90 percent of the samples. All trace-element concentrations measured were below the maximum contaminant levels set by the U.S. Environmental Protection Agency. Five samples exceeded the proposed maximum contaminant level of 0.02 milligram per liter for uranium. All samples collected exceeded the proposed maximum contaminant level for radon-222. The volatile organic compound methyltertbutylether was detected in one sample at a concentration of 0.6 microgram per liter. Of the pesticides analyzed for, one or more were detected in water from 5 of the 35 wells sampled. Metribuzin was the most commonly detected pesticide and was detected in water from three wells at concentrations ranging from an estimated 0.005 to 0.017 microgram per liter. Metolachlor (detected in one sample at a concentration of 0.072 microgram per liter), prometon (detected in one sample at a concentration of 0.01 microgram per liter), and p,p'-DDE (detected in one sample at an estimated concentration of 0.002 microgram per liter) were the other pesticides detected. The U.S. Environmental Protection Agency lifetime health advisory for metolachlor, metribuzin, and prometon is 100 micrograms per liter, which is much larger than the concentrations measured in the shallow ground water sampled for this study. The elevated nitrite plus nitrate concentrations in shallow ground water are indicative of leaching of fertilizers from the land surface. This conclusion is consistent with conclusions made in other investigations of the San Luis Valley.

Colorado↗

Guidelines and standard procedures for studies of ground-water quality; selection and installation of wells, and supporting documentation

This is the first of a two-part report to document guidelines and standard procedures of the U.S. Geological Survey for the acquisition of data in ground-water-quality studies. This report provides guidelines and procedures for the selection and installation of wells for water-quality studies/*, and the required or recommended supporting documentation of these activities. Topics include (1) documentation needed for well files, field folders, and electronic files; (2) criteria and information needed for the selection of water-supply and observation wells, including site inventory and data collection during field reconnaissance; and (3) criteria and preparation for installation of monitoring wells, including the effects of equipment and materials on the chemistry of ground-water samples, a summary of drilling and coring methods, and information concerning well completion, development, and disposition.

Water-Resources Investigations Report↗

Distribution of methyl tert-butyl ether (MTBE) and selected water-quality constituents in the surficial aquifer at the Dover National Test Site, Dover Air Force Base, Delaware, 2001

A joint study by the Dover National Test Site, Dover Air Force Base, Delaware, and the U.S. Geological Survey was conducted from June 27 through July 18, 2001, to determine the spatial distribution of the gasoline oxygenate additive methyl tert-butyl ether and selected water-quality constituents in the surficial aquifer underlying the Dover National Test Site. This report provides a summary assessment of the distribution of methyl tert-butyl ether and a preliminary screening of selected constituents that may affect natural attenuation and remediation demonstrations at the Dover National Test Site. The information gathered during this study is designed to assist potential remedial investigators who are considering conducting a methyl tert-butyl ether remedial demonstration at the test site. In addition, the study supported a planned enhanced bioremediation demonstration and assisted the Dover National Test Site in identifying possible locations for future methyl tert-butyl ether remediation demonstrations. A direct-push drill rig was used to collect a total of 147 ground-water samples (115 VOC samples and 32 quality-assurance samples) at varying depths. Volatile organic compounds were above the method reporting limits in 59 of the 115 ground-water samples. The concentrations ranged from below detection limits to maximum values of 12.4 micrograms per liter of cis-1,2-dichloro-ethene, 1.14 micrograms per liter of trichloro-ethene, 2.65 micrograms per liter of tetrachloro-ethene, 1,070 micrograms per liter of methyl tert-butyl ether, 4.36 micrograms per liter of benzene, and 1.8 micrograms per liter of toluene. Vinyl chloride, ethylbenzene, p,m-xylene, and o-xylene were not detected in any of the samples collected during this investigation. Methyl tert-butyl ether was detected in 47 of the 115 ground-water samples. The highest concentrations of methyl tert-butyl ether were detected in the surficial aquifer from ?4.6 to 6.4 feet mean sea level; however, methyl tert-butyl ether was detected as deep as ?9.5 feet mean sea level. Increased methane concentrations and decreased dissolved oxygen concentrations that were found in association with the ground-water samples that contained methyl tert-butyl ether are preliminary indicators that will assist in determining if natural attenuation of methyl tert-butyl ether is occurring in the surficial aquifer. A full assessment of natural attenuation of methyl tert-butyl ether at the site is beyond the scope of this study, but the data collected during the study will be useful in selecting appropriate remedial methyl tert-butyl ether demonstrations.

Delaware↗

Water quality data for selected wells in the Coastal Plain of New Jersey, 1996-98

Water-quality data were collected during 1996-98 for 217 wells in New Jersey and 3 wells in New York as part of the U. S. Geological Survey's National Water Quality Assessment Program. Samples were collected for five ground-water surveys that were designed to assess water quality in major aquifer systems, with an emphasis on recently recharged (shallow) ground water associated with present and recent human activities. This report (1) summarizes the hydrogeologic framework in the areas of data collection; (2) describes the objectives and procedures for designing each ground-water survey; (3) summarizes the procedures and protocols for data collec-tion, analysis, and quality control; and (4) lists the concentrations of inorganic constituents, volatile organic compounds, pesticides, nutrients, and trace elements present in the ground-water samples.

Open-File Report↗

Records and water-level measurements of selected wells and chemical analysis of ground water, East Shore area, Davis, Weber, and Box Elder Counties

This report is intended to serve two purposes: (1) to make available to the public basic ground-water data useful in planning and studying development of water resources and (2) to supplement an interpretive report that will be published later. Records were collected during the period 1935-61 by the U.S. Geological Survey in cooperation with the Utah State Engineer as a part of the investigation of the ground-water resources of the East Shore area in Davis, Weber, and southern Box Elder Counties, Utah. During the period 1952-61 additional records were collected by the U.S. Bureau of Reclamation. The interpretive material will be published cooperatively by the U.S. Geological Survey and the Utah State Engineer as a report entitled "Groundwater conditions in the East Shore area, Utah, 1953-61," by Ralph E. Smith. This report is most useful in predicting conditions likely to be found in areas that are being considered as well sites. The person considering the new well can spot the proposed site on plate 1 and examine the records of nearby wells as shown on the tables and figures. From table 1 he can note (1) the depth and diameter of wells in the vicinity and the yield of some of those wells, and (2) the depth to water or the feet of water pressure in wells in the vicinity; from table 2 and figure 2 he may note the historic fluctuations and trends of water levels in the vicinity; and from tables 3 and l he may note the chemical quality of the water from wells in the vicinity and the use made of this water. If the reader decides from his examination that conditions are favorable, he may place an application to drill a well with the State Engineer. If the State Engineer believes unappropriated water is available, the application may be approved after minimum statutory requirements have been satisfied. The report is also useful when planning large-scale developments of water supply. This and other uses of the report will be helped by use of the interpretive report upon its release.

Utah↗

Ground-water investigations of the Project Gnome area, Eddy and Lea Counties, New Mexico

The U.S. Atomic Energy Commission, through the Office of Test Operations, Albuquerque Operations Office, plans to detonate a nuclear device in a massive salt bed 1,200 feet beneath the land surface. The project, known as Project Gnome, is an element of the Plowshare program--a study of peacetime applications of nuclear fission. The location of the proposed underground shot is in a sparsely-populated area in southeastern Eddy County, N. Mex., east of the Pecos River and about 25 miles southeast of the city of Carlsbad. The area is arid to Semiarid and ground water is a vital factor in the economic utilization of the land, which is primarily used for stock raising. An investigation of the Project Gnome site and surrounding area for the purposes of evaluating the ground-water resources and the possible effect upon them from the detonation of the nuclear shot was desired by the Commission. This report describes work done by the U.S. Geological Survey on behalf of the Commission and presents results of the investigation of the ground-water resources and geology of the area. The most intensive investigations were made within a 15-mile radius of the site of Project Gnome and mainly on the east side of the Pecos River. The total area of study of over 1,200 square miles includes parts of Eddy and Lea Counties, N. Mex. The Project Gnome site is in the sedimentary Delaware Basin. It is underlain by about 18,000 feet of sedimentary rocks ranging in age from Ordovician to Recent. Upper Permian evaporitic rocks, which contain the principal source of potash available in the United States, are worked in nearby mines. The potash minerals are found in a massive salt bed about 1,400 feet thick in the Salado Formation of Permian age. The land surface of the area is covered mostly by a wind-blown sand and caliche; however, rocks of the Rustler Formation of Permian age and younger rocks of Permian, Triassic, Pleistocene(?) and Recent age crop out at several localities. Solution by ground water of salt at the top of the Salado Formation and of anhydrite within the Rustler Formation has removed thick sections of these rocks. A subsequent lowering of the land surface and differential collapse of the Rustler has formed many sinkholes and has created a karst topography over much of the western part of the area. Ground water is obtained from rocks of Permian, Triassic, Tertiary, and Quaternary age in the general region. However, the only aquifer at the Gnome site is the Culebra Dolomite Member of the Rustler Formation of Permian age. The aquifer is about 500 feet beneath the surface at the site and is about 30 feet thick. An aquifer, immediately above the top of the salt, contains a brine solution in Nash Draw, a few miles west of the Gnome site. This aquifer discharges into the Pecos River and is a major source of contamination of the river water. No potable water is known to be present in the area below the top of the salt of the Salado Formation. The ground water in the area is generally under artesian pressure. The general direction of ground-water movement is toward the Pecos River both east and west of the river. At the Gnome site the artesian head of the water in the Culebra Dolomite Member is about 7.5 feet. The water moves westward through the aquifer at a rate of about ? foot per day. The most widespread utilization of ground water east of the river is for stock use. Irrigation usage west of the Pecos River accounts for the largest withdrawal of water. Wells range in depth from a few tens of feet to nearly 800 feet. Water levels range from a few feet to about 500 feet below the surface. A test well at the Gnome site drawing water from the Culebra Dolomite Member was pumped at a rate of 100 gpm (gallons per minute); however, most wells east of the river yield only a few gpm. Irrigation wells west of the river yield as much as 3,500 gpm. Most of the water in the area is highly mineralized and is suitable only for use by livest

Open-File Report↗

Water resources data, Maryland and Delaware, water year 1997, volume 2. ground-water data

The Water Resources Division of the U.S. Geological Survey, in cooperation with State agencies, obtains a large amount of data pertaining to the water resources of Maryland and Delaware each water year. These data, accumulated during many water years, constitute a valuable data base for developing an improved understanding of the water resources of the State. To make these data readily available to interested parties outside the U.S. Geological Survey, the data are published annually in this report series entitled 'Water Resources Data - Maryland and Delaware.' This series of annual reports for Maryland and Delaware began with the 1961 water year with a report that contained only data relating to the quantities of surface water. For the 1964 water year, a similar report was introduced that contained only data relating to water quality. Beginning with the l975 water year, the report format was changed to present, in one volume, data on quantities of surface water, quality of surface and ground water, and ground-water levels. In the 1989 water year, the report format was changed to two volumes. Both volumes contained data on quantities of surface water, quality of surface and ground water, and ground-water levels. Volume 1 contained data on the Atlantic Slope Basins (Delaware River thru Patuxent River) and Volume 2 contained data on the Monongahela and Potomac River basins. Beginning with the 1991 water year, Volume 1 contains all information on quantities of surface water and surface- water-quality data and Volume 2 contains ground-water levels and ground-water-quality data. This report is Volume 2 in our 1998 series and includes records of water levels and water quality of ground-water wells and springs. It contains records for water levels at 397 observation wells, discharge data for 6 springs, and water quality at 107 wells. Location of ground-water level wells are shown on figures 3 and 4. The location for the ground-water-quality sites are shown on figures 5. These data represent that part of the National Water Data System collected by the U.S. Geological Survey and cooperating State and Federal agencies in Maryland and Delaware. Prior to introduction of this series and for several water years concurrent with it, water resources data for Maryland and Delaware were published in U.S. Geological Survey Water-Supply Papers. Data on water levels for the 1935 through 1974 water years were published under the title 'Ground-Water Levels in the United States.' The above mentioned Water-Supply Papers may be consulted in the libraries of the principal cities of the United States and may be purchased from the Branch of Information Services, Federal Center, Bldg. 41, Box 25286, Denver, CO 80225-0286. Publications similar to this report are published annually by the Geological Survey for all States. These official Survey reports have an identification number consisting of the two-letter State abbreviation, the last two digits of the water year, and the volume number. For example, this volume is identified as 'U.S. Geological Survey Water-Data Report MD-DE-98-2.' For archiving and general distribution, the reports for l971- 74 water years also are identified as water data reports. These water-data reports are for sale in paper copy or in microfiche by the National Technical Information Service, U.S. Department of Commerce, Springfield, VA 22161. Additional information, including current prices, for ordering specific reports may be obtained from the District Chief at the address given on the back of the title page or by telephone (410)238-4200.

Water Data Report↗

Determination of pharmaceutical compounds in surface- and ground-water samples by solid-phase extraction and high-performance liquid chromatography-electrospray ionization mass spectrometry

Commonly used prescription and over-the-counter pharmaceuticals are possibly present in surface- and ground-water samples at ambient concentrations less than 1 μg/L. In this report, the performance characteristics of a combined solid-phase extraction isolation and high-performance liquid chromatography–electrospray ionization mass spectrometry (HPLC–ESI-MS) analytical procedure for routine determination of the presence and concentration of human-health pharmaceuticals are described. This method was developed and used in a recent national reconnaissance of pharmaceuticals in USA surface waters. The selection of pharmaceuticals evaluated for this method was based on usage estimates, resulting in a method that contains compounds from diverse chemical classes, which presents challenges and compromises when applied as a single routine analysis. The method performed well for the majority of the 22 pharmaceuticals evaluated, with recoveries greater than 60% for 12 pharmaceuticals. The recoveries of angiotensin-converting enzyme inhibitors, a histamine (H2) receptor antagonist, and antihypoglycemic compound classes were less than 50%, but were retained in the method to provide information describing the potential presence of these compounds in environmental samples and to indicate evidence of possible matrix enhancing effects. Long-term recoveries, evaluated from reagent-water fortifications processed over 2 years, were similar to initial method performance. Method detection limits averaged 0.022 μg/L, sufficient for expected ambient concentrations. Compound-dependent matrix effects on HPLC/ESI-MS analysis, including enhancement and suppression of ionization, were observed as a 20–30% increase in measured concentrations for three compounds and greater than 50% increase for two compounds. Changing internal standard and more frequent ESI source maintenance minimized matrix effects. Application of the method in the national survey demonstrates that several pharmaceuticals are routinely detected at 0.010–0.100 μg/L concentrations.

Journal of Chromatography A↗