Ground-water levels and their relationship to ground-water problems in Suffolk County, Long Island, New York
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Geohydrologic and water-quality data collected during 1997 through 2000 in the vicinity of a former waste-oil refinery near Westville, Indiana, define a plume of 1,4-dioxane in ground water that extends to the southwest approximately 0.8 miles from the refinery site. Concentrations of 1,4-dioxane in the plume ranged from 3 to 31,000 micrograms per liter. Ground water containing 1,4-dioxane is discharged to Crumpacker Ditch, approximately one-half mile west of the refinery site. Concentrations of 1,4-dioxane detected in surface water ranged from 8 to 140 micrograms per liter; 1,4-dioxane also is transported in ground water beneath the ditch. The study area is underlain by glacial deposits of sand and gravel that overlie lacustrine clay and shale. The sand and gravel deposits form an extensive aquifer ranging from 148 to 215 feet thick in the study area. Ground water generally flows from northeast to southwest and the depth to water ranges from about 3 to 36 feet below land surface. The average horizontal hydraulic conductivity of the aquifer, determined from a multiple-well aquifer test, was 121 feet per day, and the transmissivity was 18,600 feet squared per day. Vertical hydraulic conductivity ranged from 24 to 36 feet per day and specific yield ranged from 0.05 to 0.08. Analysis of single-well aquifer tests indicated that horizontal hydraulic conductivity ranged from 0.6 to 127 feet per day and was largest in the lower part of the aquifer. Horizontal gradients averaged about 0.001 feet per foot; estimated ground-water- flow velocities averaged about 0.1 feet per day in the upper and middle parts of the glacial aquifer and about 0.4 feet per day near the bottom of the aquifer. Analytical results of water samples indicate the ground water generally is a calcium-bicarbonate type with a nearly neutral pH. Specific conductivity ranged from 437 to 1,030 microsiemens per centimeter at 25 degrees Celsius in water from wells upgradient from the refinery site and 330 to 3,780 microsiemens per centimeter at 25 degrees Celsius in water from downgradient wells. Barium, iron, manganese, nickel, and zinc commonly were detected in samples of ground water. Volatile organic compounds (including chlorinated solvents and aromatic hydrocarbons) were consistently detected in samples from shallow wells near the boundaries of the former refinery site. Concentrations of 1,4-dioxane were detected in water from wells screened in the upper, middle, and lower parts of the aquifer downgradient from the site and in samples of surface water collected approximately 5 miles downstream from where the plume intersects Crumpacker Ditch. A three-dimensional, four layer groundwater- flow model was constructed and calibrated to match ground-water levels and streamflow measured during December 1997. The model was used to simulate possible mechanisms of contaminant release, the effect of increased pumpage from water-supply wells, and pumping at the leading edge of the plume as a possible means of remediation. Based on simulation of three waste-oil lagoons, a vertical hydraulic conductivity of 0.2 feet per day was required to move contaminants into the bottom layer of the model at a constant leakage rate of about 98 gallons per minute. Simulations of a disposal well in layer 3 of the model indicated an injection rate of 50 gallons per minute was necessary to spread contaminants vertically in the aquifer. Simulated pumping rates of about 300 and 1,000 gallons per minute were required for water supply wells at the Town of Westville and the Westville Correctional Facility to draw water from the plume of 1,4-dioxane. Simulated pumping from hypothetical wells at the leading edge of the plume indicated that three wells, each pumping 25 gallons per minute from model layer 3, would capture the plume of 1,4-dioxane.
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Water-resources data for the 2003 water year for New Jersey are presented in three volumes, and consists of records of stage, discharge, and water quality of streams: stage, contents, and water quality of lakes and reservoirs; and water levels and water quality of ground water. Volume 2 contains a summary of the hydrologic conditions for 2003 water year; a listing of current water resource projects in New Jersey; a bibliography of water-related reports, articles, and fact sheets completed by the Geological Survey in recent years; records of ground-water levels from 185 wells; and a table of discontinued observation wells for which ground-water-level data are available. The locations of the ground-water level sites are shown on figure 4. These data represent that part of the National Water Data System operated by the U.S. Geological Survey and cooperating Federal, Sate, and local agencies in New Jersey.
Water-resources data for the 2004 water year for New Jersey are presented in three volumes, and consists of records of stage, discharge, and water quality of streams: stage, contents, and water quality of lakes and reservoirs; and water levels and water quality of ground water. Volume 2 contains a summary of the hydrologic conditions for 2004 water year; a listing of current water resource projects in New Jersey; a bibliography of water-related reports, articles, and fact sheets completed by the Geological Survey in recent years; records of ground-water levels from 196 wells; and a table of discontinued observation wells for which ground-water-level data are available. The locations of the ground-water level sites are shown on figure 4. These data represent that part of the National Water Data System operated by the U.S. Geological Survey and cooperating Federal, Sate, and local agencies in New Jersey.
Water-resources data for the 1998 water year for New Jersey are presented in three volumes, and consists of records of stage, discharge, and water quality of streams; stage, contents, and water quality of lakes and reservoirs; and water levels and water quality of ground water. Volume 2 contains a summary of the hydrologic conditions for 1998 water year; a listing of current water resource projects in New Jersey; a bibliography of water-related reports, articles, and fact sheets completed by the Geological Survey in recent years; records of ground-water levels from 190 wells; and a table of discontinued observation wells for which ground-water-level data are available. The locations of the ground-water level sites are shown on figure 3. These data represent that part of the National Water Data System operated by the U.S. Geological Survey and cooperating Federal, State, and local agencies in New Jersey.
The central Sevier Valley, in the central part of Utah, extends from the town of Kingston to the Yuba Dam and from the Tushar and Valley Mountains and the Pavant Range to the Sevier, Fishlake, Wasatch, and Gunnison Plateaus. A geologic and hydrologic investigation of the valley was made to determine the relation between surface water and ground water and to determine if ground water can be used for irrigation supplies without affecting existing water uses. During the investigation, data were collected for about 700 wells and 26 springs. Monthly water-level measurements were made at 93 observation wells, and automatic recording gages were maintained at 6 additional wells. Chemical analyses were made of water collected from 68 wells and springs. Test holes were drilled at 21 sites to determine the thickness and hydrologic properties of the waterbearing materials. Consumption of ground water by vegetation was estimated on the basis of area and applied rates of evapotranspiration.
Water resources data for Iowa for the 1998 water year consists of records of stage, discharge, and water quality of streams; stage, and/or contents of lakes and reservoirs; ground water levels and water quality of ground-water wells. This report volume contains discharge records for 32 gaging stations; stage or contents for 2 lakes; water quality for 1 stream-gaging station, and sediment records for 3 stream-gaging stations. Also included are data for 34 crest-stage partial record stations and ground-water levels for 176 wells. Additional water data were collected at various sites, but are not part of the systematic data collection program and are published as miscellaneous discharge and miscellaneous water-quality analyses.
A study of the Hillsborough River watershed was conducted between October 1999 through September 2003 to characterize the hydrology, water quality, and interaction between the surface and ground water in the highly karstic uppermost part of the watershed. Information such as locations of ground-water recharge and discharge, depth of the flow system interacting with the stream, and water quality in the watershed can aid in prudent water-management decisions. The upper Hillsborough River watershed covers a 220-square-mile area upstream from Hillsborough River State Park where the watershed is relatively undeveloped. The watershed contains a second order magnitude spring, many karst features, poorly drained swamps, marshes, upland flatwoods, and ridge areas. The upper Hillsborough River watershed is subdivided into two major subbasins, namely, the upper Hillsborough River subbasin, and the Blackwater Creek subbasin. The Blackwater Creek subbasin includes the Itchepackesassa Creek subbasin, which in turn includes the East Canal subbasin. The upper Hillsborough River watershed is underlain by thick sequences of carbonate rock that are covered by thin surficial deposits of unconsolidated sand and sandy clay. The clay layer is breached in many places because of the karst nature of the underlying limestone, and the highly variable degree of confinement between the Upper Floridan and surficial aquifers throughout the watershed. Potentiometric-surface maps indicate good hydraulic connection between the Upper Floridan aquifer and the Hillsborough River, and a poorer connection with Blackwater and Itchepackesassa Creeks. Similar water level elevations and fluctuations in the Upper Floridan and surficial aquifers at paired wells also indicate good hydraulic connection. Calcium was the dominant ion in ground water from all wells sampled in the watershed. Nitrate concentrations were near or below the detection limit in all except two wells that may have been affected by fertilizer or animal waste. Wells at the Blackwater Creek and Hillsborough River at State Road 39 transects showed little seasonal variation in dissolved organic carbon. Dissolved organic carbon concentrations, however, were greater during the wet season than during the dry season at the Hillsborough River Tract transect, indicating some influence from surface-water sources. During dry periods, streamflow in the upper Hillsborough River was sustained by ground water from the underlying Upper Floridan aquifer. During wet periods, streamflow had additional contributions from runoff, and release of water from extensive riverine wetlands, and by overflow from the Withlacoochee River. In contrast, streamflow in Blackwater and Itchepackesassa Creeks was less constant, with many no-flow days occurring during dry periods. During wet season storm events, streamflow peaks occur more rapidly because there is greater confinement between the surficial deposits and the Upper Floridan aquifer, and these creeks have been highly channelized, leaving less of the adjacent wetlands intact. During dry periods, Blackwater Creek is dry upstream from its confluence with Itchepackesassa Creek, and all downstream flow is from Itchepackesassa Creek. Much of the dry season flow in Itchepackesassa Creek originates from a treated wastewater effluent outfall located on East Canal. Long-term streamflow at the Hillsborough River and Blackwater Creek stations was greater than the discharge observed during the study period. Water quality in the upper Hillsborough River is influenced by ground-water discharge. The chemical composition of water from Blackwater Creek, Itchepackesassa Creek, and East Canal was more variable because there was less ground-water discharge to these creeks than to the upper Hillsborough River, and because of the influence of wastewater effluent. Strontium isotope data indicated that the source of the water at all Hillsborough River sites during the dry season was the Oli
Commonly measured water quality parameters were compared to heat as tracers of stream water exchange with ground water. Temperature, specific conductance, and chloride were sampled at various frequencies in the stream and adjacent wells over a 2-year period. Strong seasonal variations in stream water were observed for temperature and specific conductance. In observation wells where the temperature response correlated to stream water, chloride and specific conductance values were similar to stream water values as well, indicating significant stream water exchange with ground water. At sites where ground water temperature fluctuations were negligible, chloride and/or specific conductance values did not correlate to stream water values, indicating that ground water was not significantly influenced by exchange with stream water. Best-fit simulation modeling was performed at two sites to derive temperature-based estimates of hydraulic conductivities of the alluvial sediments between the stream and wells. These estimates were used in solute transport simulations for a comparison of measured and simulated values for chloride and specific conductance. Simulation results showed that hydraulic conductivities vary seasonally and annually. This variability was a result of seasonal changes in temperature-dependent hydraulic conductivity and scouring or clogging of the streambed. Specific conductance fits were good, while chloride data were difficult to fit due to the infrequent (quarterly) stream water chloride measurements during the study period. Combined analyses of temperature, chloride, and specific conductance led to improved quantification of the spatial and temporal variability of stream water exchange with shallow ground water in an alluvial system.
Water resources data for the 1998 water year for Maryland and Delaware consist of records of water levels and water quality of ground-water wells. This report (Volume 2. Ground-Water Data) contains water levels at 393 observation wells, discharge records for 6 springs and water quality at 290 wells and 23 streambed piezometers. Locations of ground-water level wells are shown on figures 5 and 6. Locations of ground-water-quality sites are shown on figure 7. The data in this report represent that part of the National Water Data System collected by the U.S. Geological Survey and cooperating State, local, and Federal agencies in Maryland and Delaware.
Water resources data for the 2000 water year for Maryland and Delaware consist of records of water levels and water quality of ground-water wells. This report (Volume 2. Ground-Water Data) contains water levels at 347 observation wells, discharge records for 5 springs, and water quality at 225 wells, 13 piezometers, and 4 springs. Locations of ground-water level wells are shown on figures 5 and 6. Locations of ground-water-quality sites are shown on figure 7. The data in this report represent that part of the National Water Data System collected by the U.S. Geological Survey and cooperating State, local, and Federal agencies in Maryland and Delaware.
Water resources data for the 1999 water year for Maryland and Delaware consist of records of water levels and water quality of ground-water wells. This report (Volume 2. Ground-Water Data) contains water levels at 395 observation wells, discharge records for 6 springs and water quality at 1 spring, 186 wells, and 27 streambed piezometers. Locations of ground-water level wells are shown on figures 5 and 6. Locations of ground-water-quality sites are shown on figure 7. The data in this report represent that part of the National Water Data System collected by the U.S. Geological Survey and cooperating State, local, and Federal agencies in Maryland and Delaware.
Water from 265 domestic wells that tap the unconfined Kirkwood-Cohansey aquifer system in the Coastal Plain of New Jersey contained concentrations of mercury that are equal to or exceed the U.S. Environmental Protection Agency maximum contaminant level (MCL) of 2 ug/L (micrograms per liter). The wells range in depth from 50 to 200 feet, and are located in 32 discrete, mostly residential, areas that were developed primarily on former agricultural land during the 1950?s through the 1970?s. Concentrations in two other areas exceeded 1 ug/L. Naturally occurring mercury concentrations in ground water from the Kirkwood-Cohansey aquifer system typically are less than 0.01 ug/L, but concentrations in water from some wells were as much as 42 ug/L. No evidence currently exists that conclusively links known point sources such as landfills, industrial operations, or commercial enterprises to most of the elevated concentrations of mercury in ground water in the residential areas. Possible sources of the mercury include pesticides and atmospheric deposition. Analysis of water from wells in 6 of the 34 areas for other constituents indicates that nitrate concentrations also commonly are elevated above background levels (which typically are undetectable at 0.01 milligrams per liter), and exceed the MCL of 10 milligrams per liter in some samples. Several volatile organic compounds (VOCs), including chloroform, also have been measured in water from wells at many of the 34 sites. Analytical results for water samples collected at several depths from boreholes at 2 of the 34 sites indicate elevated concentrations of calcium, magnesium, barium, strontium, nitrate, and chloride, which may be related to both agricultural chemical applications and septic-system effluent. Determinations of tritium and helium concentrations indicate that water containing elevated concentrations of mercury recharged the aquifer between 9.4 and 79 years ago, which includes the period during which many of the 34 sites were undergoing a change from agricultural or undeveloped to residential land use. Batch equilibrium experiments were used to measure adsorption of dissolved mercury, mercuric chloride, and phenylmercuric acetate by aquifer sediments at pH 3.5-4.0, 4.5-5.0, and 5.5-6.0. In nearly all cases, 55 to 95 percent of the mercury added to the sediments was adsorbed. Mercury mobilization from aquifer sediments inoculated with mercury was investigated by leaching the sediments with two concentrations of nitric acid (a component of acid rain), a sodium chloride solution (simulating road salt), and three fertilizer solutions. A solution of 20-20-20 (nitrogenphosphorous-potassium) fertilizer removed virtually all of the mercury with which the sediments had been inoculated. The sodium chloride solution was moderately effective in removing applied mercury from the sediments, as was a solution of nitric acid. A more dilute nitric acid solution and two sodium nitrate fertilizer solutions were less effective. Results of these experiments indicate that mercury adsorbs to aquifer sediments, but that varying amounts can be removed by infiltrating solutions, some of which can be related to specific land uses. Land-use history at the 34 sites generally indicates a change from agricultural or undeveloped settings to residential settings. Whatever the source of mercury to these sites, a change in the geochemical environment of the soil and aquifer brought about by land-use change probably provides mechanisms for mobilizing the mercury from soils and sediments to ground water.
Ground water vulnerability maps developed using the DRASTIC method have been produced in many parts of the world. Comparisons of those maps with actual ground water quality data have shown that the DRASTIC method is typically a poor predictor of ground water contamination. This study significantly improved the effectiveness of a modified DRASTIC ground water vulnerability map by calibrating the point rating schemes to actual ground water quality data by using nonparametric statistical techniques and a geographic information system. Calibration was performed by comparing data on nitrite plus nitrate as nitrogen (NO 2 + NO 3 -N) concentrations in ground water to land-use, soils, and depth to first-encountered ground water data. These comparisons showed clear statistical differences between NO 2 + NO 3 -N concentrations and the various categories. Ground water probability point ratings for NO 2 + NO 3 -N contamination were developed from the results of these comparisons, and a probability map was produced. This ground water probability map was then correlated with an independent set of NO 2 + NO 3 -N data to demonstrate its effectiveness in predicting elevated NO 2 + NO 3 -N concentrations in ground water. This correlation demonstrated that the probability map was effective, but a vulnerability map produced with the uncalibrated DRASTIC method in the same area and using the same data layers was not effective. Considerable time and expense have been outlaid to develop ground water vulnerability maps with the DRASTIC method. This study demonstrates a cost-effective method to improve and verify the effectiveness of ground water vulnerability maps.
In 1978 the U.S. Geological Survey began a 5-year study of the High Plains regional aquifer system to provide hydrologic information for evaluating the effects of long-term development of the aquifer and to develop a capability for predicting aquifer response to alternative changes in ground-water management. By use of a digital model, this report presents a quantitative description of the High Plains aquifer in Oklahoma. The High Plains aquifer consists predominantly of the Tertiary Ogallala Formation and overlying Quaternary alluvium and terrace deposits which are hydraulically connected to the High Plains aquifer. Much of the aquifer is underlain by formations of Permian through Cretaceous age, which generally have very small hydraulic conductivities. In some areas parts of underlying Triassic, Jurassic, or Cretaceous rocks are hydraulically connected with the aquifer. The High Plains aquifer is a water-table aquifer in which water moves generally to the east-southeast. Before the beginning of extensive irrigation of the 1960's, the aquifer was essentially in dynamic equilibrium with recharge from precipitation balanced by natural discharge from the aquifer. Ground-water discharge appeared in streams leaving the area or was returned to the atmosphere through evapotranspiration. Accurate records of irrigation pumpage are not available from the High Plains. In order to estimate irrigation pumpage, published records of crop distribution were used and a consumptive use was assigned to each principal irrigated crop. This method gave an estimated irrigation demand. Pumpage was taken as a percentage of the total irrigation demand. Irrigation has decreased ground-water discharge from the High Plains aquifer. Ground-water discharge was estimated as approximately 118 cubic feet per second in 1980. A finite-difference digital model was used to simulate flow in the High Plains aquifer. The recharge was adjusted so that 1980 ground-water discharge was 118 cubic feet per second, the estimated ground-water discharge for 1980. Recharge in the eastern half of the modeled area was 0.45 inch per year; one-half this value was used in the western half of the modeled area. Hydraulic conductivity was divided into three zones: 19.3 feet per day in the eastern zone; 16.2 feet per day in the central zone; and 8.28 feet per day in the western zone. A specific yield of 14.7 percent was used in the model. Using all these parameters, the model was calibrated so that the mean difference between predevelopment modeled and measured head was -0.044 foot. Following the calibration procedure, the model was used to predict the volumes of water in storage and distribution of saturated thickness in 1993 and 2020 using the 1980 pumping rates. The calculated quantity of water in storage in the aquifer in 1941 (predevelopment) was approximately 135.2 million acre-feet; in 1980, approximately 121.9 million acre-feet; in 1993 approximately 112.7 million acre-feet; and in 2020, approximately 96.2 million acre-feet. The High Plains aquifer in Oklahoma will continue to be an important source of water past the year 2000. As withdrawals continue from the aquifer at the present rate, the water table will continue to decline and when the water table drops below the streambed in any part of the area, ground-water discharge to streams will cease in that area. Based on the calculated volumes of water in storage, the volume of water remaining in storage as compared to the predevelopment volume is as follows: 90 percent in 1980, 83 percent in 1993, and 71 percent in 2020.
Analyses of water samples collected since 1934 from some of the irrigation wells in the Lompoc subarea of the Santa Ynes River valley have shown a gradual deterioration in the chemical quality of the water. Most of the ground water pumped in the subarea has a dissolved-solids contents ranging from about 700 to about 2,000 parts per million, of which sulfate and chloride are the predominant constituents. Suitability of the water for irrigation is variable and is dependent principally on "potential salinity" of the water, soil permeability, and type of crop. Changes in water quality are not consistent throughout the subarea. No doubt the chloride concentration increases as a result of both the recycling irrigation water and inflow of high-chloride low-sulfate connate water from the consolidated Tertiary rocks. The influence of recycled irrigation water is indicated by increase concentrations of chloride and sulfate in a ratio of 1:2. Inflow of high-chloride low-sulfate connate water is indicated by increased chloride concentration correlated with little or no change in sulfate concentration. Peak chloride concentrations in three local areas are probably the result of the inflow of connate water. Furthermore, ground-water gradients in each of the local areas are favorable for inflow from the consolidated rocks.
Water resources data for the 1997 water year for Wyoming consists of records of stage, discharge and water quality of streams; stage and contents of lakes and reservoirs, and water levels and water quality of ground water. Volume 2 of this report contains water levels records for 82 wells. Additional ground-water data were collected at various sites, not part of the systematic data collection program, and are published as miscellaneous studies and programs. These data together with the data in Volume 1 represent part of the National Water Data System operated by theU.S. Geological Survey and cooperating State and Federal agencies in Wyoming.