Geology Reports⌕ Search

SEARCH · Geology Reports

Results for “Chemistry and Water”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,081 records · Page 60Linked to original sources
USGS2022

Sensitivity of headwater streamflow to thawing permafrost and vegetation change in a warming Arctic

Climate change has the potential to impact headwater streams in the Arctic by thawing permafrost and subsequently altering hydrologic regimes and vegetation distribution, physiognomy and productivity. Permafrost thaw and increased subsurface flow have been inferred from the chemistry of large rivers, but there is limited empirical evidence of the impacts to headwater streams. Here we demonstrate how changing vegetation cover and soil thaw may alter headwater catchment hydrology using water budgets, stream discharge trends, and chemistry across a gradient of ground temperature in northwestern Alaska. Colder, tundra-dominated catchments shed precipitation through stream discharge, whereas in warmer catchments with greater forest extent, evapotranspiration and infiltration are substantial fluxes. Forest soils thaw earlier, remain thawed longer, and display seasonal water content declines, consistent with greater evapotranspiration and infiltration. Streambed infiltration and water chemistry indicate that even minor warming can lead to increased infiltration and subsurface flow. Additional warming, permafrost loss, and vegetation shifts in the Arctic will deliver water back to the atmosphere and to subsurface aquifers in many regions, with the potential to substantially reduce discharge in headwater streams, if not compensated by increasing precipitation. Decreasing discharge in headwater streamflow will have important implications for aquatic and riparian ecosystems.

Alaska↗
USGS2007

Influence of Locally Derived Recharge on the Water Quality and Temperature of Springs in Hot Springs National Park, Arkansas

The hot springs of Hot Springs National Park consist of a mixture of water from two recharge components: a primary hot-water component and a secondary cold-water component. Widespread distribution of fractures enables mixing of the hot- and cold-water components of flow near the discharge area for the springs. Urbanization in the area near the hot springs of Hot Springs National Park has increased the potential for degradation of the quality of surface-water runoff and locally derived ground-water recharge to the hot springs. Previous studies by the U.S. Geological Survey have indicated that water from some cold-water springs and wells in the vicinity of Hot Springs, Arkansas, showed evidence of contamination and that water from locally derived cold-water recharge might contribute 25 percent of the total flow to the hot springs after storms. Water samples were collected during base-flow conditions at nine hot springs and two cold-water springs in September 2000. Nine hot springs and one cold-water spring were resampled in October 2001 after a storm that resulted in a measurable decrease in water temperature in selected hot springs. Water samples were analyzed for a variety of dissolved chemical constituents (nutrients, major ions, trace elements, pesticides, semivolatile compounds, isotopes, and radiochemicals), physical properties, field measurements, and bacteria. Comparison of analyses of samples collected during base-flow conditions from the springs in 2000 and during a storm event in 2001 with the results from earlier studies dating back to the late 1800's indicates that little change in major, minor, and trace constituent chemistry has occurred and that the water continues to be of excellent quality. Water-quality data show distinguishable differences in water chemistry of the springs during base-flow and stormflow conditions, indicating changing input of cold-water recharge relative to hot-water recharge. Silica, total dissolved solids, strontium, barium, and sulfate show statistically significant differences between the median values of base-flow and stormflow samples. While variations in these constituents do not degrade water quality, the differences do provide evidence of variability in the factors controlling water quality of the hot springs and show that water quality is influenced by the locally derived, cold-water component of flow to the springs. Water temperature was measured continuously (3-minute intervals) between August 2000 and October 2002 at four hot springs. Continuous water-temperature data at the springs provide no indication of persistent long-term change in water temperature through time. Short time-scale water-temperature decreases occur in response to mixing of hot-springs water with locally derived recharge after storm events; the magnitude of these decreases varied inversely with the amount of rainfall. Maximum decreases in water temperature for specific storms had a non-linear relation with the amount of precipitation measured for the events. Response time for water temperature to begin decreasing from baseline temperature as a result of storm recharge was highly variable. Some springs began decreasing from baseline temperature as quickly as 1 hour after the beginning of a storm; one spring had an 8-hour minimum response time to show a storm-related temperature decrease. Water-quality, water-temperature, isotopic, and radiochemical data provide multiple lines of evidence supporting the importance of the contribution of cold-water recharge to hot springs. All the springs sampled indicated some measure of influence from local recharge. Binary mixing models using silica and total dissolved solids indicate that cold-water recharge from stormflow contributes an estimated 10 to 31 percent of the flow of hot springs. Models using water temperature indicate that cold-water recharge from stormflow contributes an estimated 1 to 35 percent of the flow of the various hot springs. Alth

Scientific Investigations Report↗
USGS2003

Evaluation of tracer tests completed in 1999 and 2000 on the upper Santa Clara River, Los Angeles and Ventura Counties, California

The interaction of surface water and hyporheic water along the Santa Clara River in Los Angeles and Ventura Counties, California, was evaluated by conducting tracer tests and analyzing water-quality data under different flow conditions in October 1999 and May 2000. Tracer and water-quality samples were collected at multiple river and hyporheic sites as well as at the Los Angeles County Sanitation Districts Saugus and Valencia Water Reclamation Plants. These water reclamation plants provide the main source of base flow in the river. Rhodamine WT dye was injected into the river to determine river traveltimes and to indicate when Lagrangian water-quality sampling could be performed at each site. Sodium bromide was injected into the river at a constant rate at the water reclamation plants to evaluate the surface-water and shallow ground-water interactions in the hyporheic zone. In the upper reach of the study area, which extends 2.9 river miles downstream from the Saugus Water Reclamation Plant, traveltime was 3.2 hours during May 2000. In the lower reach, which extends 14.1 river miles downstream from the Valencia Water Reclamation Plant, traveltime was 9.6 hours during October 1999 and 7.1 hours during May 2000. The sodium bromide tracer was detected at both hyporheic locations sampled during October 1999, and at two of the three hyporheic locations sampled during May 2000. On the basis of Rhodamine dye tests, flow curves were constructed from the discharge measurements in the Valencia reach. Flow-curve results indicate net gains in flow throughout most, but not all, of the upper parts of the reach and net losses in flow at the lower part of the reach. Lagrangian water-quality sampling provides information on the changes in chemistry as the water flows downstream from the water reclamation plants. Along both reaches there is an increase in sulfate (40-60 mg/L in the Saugus reach and 160 mg/L in the Valencia reach) and a decrease in chloride (about 45 mg/L in the Saugus reach and about 10 mg/L in the Valencia reach). The increasing sulfate concentrations are consistent with discharge of higher sulfate ground water into the river. Along both reaches there is a trend of decreasing ammonia and slightly increasing nitrate concentrations. This trend is consistent with nitrification. Samples were also analyzed for numerous compounds associated with wastewater, but analysis focused on four indicators. Concentrations of wastewater indicators in the Santa Clara River were low and decreased downstream from the reclamation plants. There is general consistency between the chemical and tracer data collected from the hyporheic and the river-aquifer flow regime within a reach. The water quality at the hyporheic site in a gaining reach of the river resembled that of the local ground water and no wastewater indicators or injected tracers were observed; whereas, the water quality at the hyporheic sites in a losing reach of the river resembled the water quality of the river at the corresponding river site, and injected tracers were observed.

California↗
USGS1999

Water resources of the Batavia Kill basin at Windham, Greene County, New York

The water resources of a 27.6-square-mile section of the Batavia Kill Basin near the village of Windham, N.Y., which has undergone substantial development, were evaluated. The evaluation entailed (1) estimation of the magnitude and distribution of several hydrologic components, including recharge, (2) measurement of discharge and chemical quality of the Batavia Kill and selected tributaries, (3) analysis of ground-water flow and chemistry, and (4) a conceptualization of the ground-water flow system. The region consists of deeply dissected, relatively flat-lying, clastic sedimentary sequences variably overlain by as much as 120 feet of glacial deposits. The types of bedrock fractures and their distribution in the Batavia Kill valley are consistent with valley stress-relief characteristics. Till predominates in the uplands, and stratified drift typically dominates within the valley of the Batavia Kill and the lower section of its largest tributary valley (Mitchell Hollow). Fractured bedrock is the most commonly used water source within the study area. The areas of highest yielding bedrock generally are with valleys, where the shallow fractures are saturated. Stratified-drift aquifers are also limited to the largest valleys; the greatest saturated thicknesses are in the Batavia Kill valley at Windham. A conceptual model of ground-water flow within the study areas suggests that the zones of most active flow are shallow fractured bedrock in upland areas and the shallow stratified drift in the largest valleys. The hydrogeologic system has been altered by development; major effects include (1) chemical alteration of natural ground-water and surface-water quality by point- and nonpoint-source contaminants, (2) hydraulic interconnection of other-wise isolated bedrock fractures by wellbores, and (3) drawdowns in wells within the Batavia Kill valley by pumping from the bedrock aquifer. Water resource development of the most promising unconsolidated aquifer beneath Windham may be precluded by the potential for contamination by leachate from an abandoned landfill, road-salt stockpiles, and domestic septic systems in the area.

New York↗
USGS2015

An evaluation of the residual toxicity and chemistry of a sodium hydroxide-based ballast water treatment system for freshwater ships

Nonnative organisms in the ballast water of freshwater ships must be killed to prevent the spread of invasive species. The ideal ballast water treatment system (BWTS) would kill 100% of ballast water organisms with minimal residual toxicity to organisms in receiving waters. In the present study, the residual toxicity and chemistry of a BWTS was evaluated. Sodium hydroxide was added to elevate pH to >11.5 to kill ballast water organisms, then reduced to pH <9 by sparging with wet-scrubbed diesel exhaust (the source of CO 2 ). Cladocerans ( Ceriodaphnia dubia ), amphipods ( Hyalella azteca ), and fathead minnows ( Pimephales promelas ) were exposed for 2 d to BWTS water under an air atmosphere (pH drifted to ≥9) or a 2.5% CO 2 atmosphere (pH 7.5–8.2), then transferred to control water for 5 d to assess potential delayed toxicity. Chemical concentrations in the BWTS water met vessel discharge guidelines with the exception of concentrations of copper. There was little to no residual toxicity to cladocerans or fish, but the BWTS water was toxic to amphipods. Maintaining a neutral pH and diluting BWTS water by 50% eliminated toxicity to the amphipods. The toxicity of BWTS water would likely be minimal because of rapid dilution in the receiving water, with subsurface release likely preventing pH rise. This BWTS has the potential to become a viable method for treating ballast water released into freshwater systems.

Environmental Toxicology and Chemistry↗
USGS2002

Interactions between groundwater and surface water: The state of the science

The interactions between groundwater and surface water are complex. To understand these interactions in relation to climate, landform, geology, and biotic factors, a sound hydrogeoecological framework is needed. All these aspects are synthesized and exemplified in this overview. In addition, the mechanisms of interactions between groundwater and surface water (GW-SW) as they affect recharge-discharge processes are comprehensively outlined, and the ecological significance and the human impacts of such interactions are emphasized. Surface-water and groundwater ecosystems are viewed as linked components of a hydrologic continuum leading to related sustainability issues. This overview concludes with a discussion of research needs and challenges facting this evolving field. The biogeochemical processes within the upper few centimeters of sediments beneath nearly all surface-water bodies (hyporheic zone) have a profound effect on the chemistry of the water interchange, and here is where most of the recent research has been focusing. However, to advance conceptual and other modeling of GW-SW systems, a broader perspective of such interactions across and between surface-water bodies is needed, including multidimensional analyses, interface hydraulic characterization and spatial variability, site-to-region regionalization approaches, as well as cross-disciplinary collaborations.

Hydrogeology Journal↗
USGS2000

Hydrogeology, water quality, and stormwater-sediment chemistry of the Grande Wash area, Fort McDowell Indian Reservation, Maricopa County, Arizona

Grande Wash is a tributary of the Verde River and drains an area of 13 square miles within the McDowell Mountains and the Town of Fountain Hills in Central Arizona. The wash enters the Fort McDowell Indian Reservation at the eastern boundary of Fountain Hills and is incised in coarse-grained alluvium that is contiguous with the alluvial aquifer along the Verde River. The aquifer is used by the Fort McDowell Indian Community and the City of Phoenix for municipal water supplies. Episodic flows in Grande Wash, in response to storms, carry potentially hazardous runoff from Fountain Hills onto the reservation. Additional potential hazards to ground water include contamination from a wastewater-treatment plant located less than 1 mile upstream from the reservation boundary, and from a landfill and a cement-processing plant immediately adjacent to the main channel of the wash. Coarse-grained deposits in Grande Wash also include recent stream-channel deposits, soil backfill, landfill material, and the upper coarse-grained layer of basin-fill sediments. Surface-geophysical surveys and drilling indicated that the coarse-grained deposits are less than 60-feet thick along the wash and in adjacent areas within the reservation, and are underlain by a thick clay and silt unit, the base of which is below the bottom of the deepest monitor well (317 feet below land surface). The coarse-grained deposits form the alluvial aquifer beneath Grande Wash. Ground water in the alluvial aquifer beneath the wash is shallow and mounded above a less permeable clay and silt unit. Depth to water in the aquifer ranges from 1 to 22 feet below land surface. Saturation of the coarse-grained deposits does not extend laterally for more than about 1,000 feet from the main channel of Grande Wash; the extent varies in response to recharge amounts. Flux of ground water through the alluvial aquifer beneath the wash is toward the Verde River and is estimated to be about 8,000 cubic feet per day (about 0.2 acre-feet per day). The flow rate is four orders of magnitude less than the flow rate in the Verde River. Vertical flux of ground water through the underlying clay and silt unit is estimated to be 7,000 cubic feet per day (0.17 acre-feet per day). The volume of ground water in storage in the alluvial aquifer beneath Grande Wash is estimated to be about 5.6 million cubic feet (129 acre-feet). Concentrations of dissolved inorganic constituents in ground water and surface water are high relative to concentrations found in the regional aquifer in surrounding areas and are indicative of salts that can be expected to be mobilized by runoff in the drainage area. Concentrations of nitrate, chloride, and sulfate are near U.S. Environmental Protection Agency Primary or Secondary Drinking-Water Regulations. Concentrations of arsenic, antimony, and strontium are below drinking-water standards but can be attributed to geologic deposits in and near the study area. Low concentrations of anthropogenic compounds, including chloroform and dichlorobromomethane, were detected. These compounds are disinfection by-products of chlorinated water. Eight pesticide compounds were detected in the surface water, and two pesticide compounds were detected in the ground water. Pesticide concentrations were below U.S. Environmental Protection Agency Maximum Contaminant Levels. Several other organic anthropogenic compounds that probably originated from commercial activities in the area were detected but at concentrations below laboratory calibration standards. Concentrations of trace metals in the stormwater sediment collected from the sediment retention basin in the lowest part of the wash were low and several were below the laboratory’s detection limits. Concentrations of most organic compounds in the stormwater sediment were below detection limits. Organic compounds present at concentrations above detection limits were p-cresol and two phthalate esters—bis (2-ethylhexyl) phthalate and dibutyl phthalate. P-cresol is used in pesticides or in disinfectants and deodorizers, and phthalate esters are commonly used in plastics, hydraulic fluid, and electric capacitors.

Arizona↗
USGS2004

Hydrogeology and Water Quality of the Pepacton Reservoir Watershed in Southeastern New York. Part 3. Responses of Stream Base-Flow Chemistry to Hydrogeologic Factors and Nonpoint-Sources of Contamination

Base-flow samples were collected seasonally from 20 small streams in the 372-square-mile Pepacton Reservoir watershed to evaluate the effects of hydrogeologic factors and nonpoint sources of contamination on the chemical composition of ground-water discharge. The reservoir provides part of New York City?s water supply. The subbasins represented one of three general types of land use, each with at least 45 percent forested area (mostly on the hillsides): farmed (dairy) land, formerly farmed land with low-density residential development, or forested land with little or no development. The subbasin areas ranged from 0.38 to 10.23 square miles. All streams were sampled in December 2000 and in May, July, and October 2001. Three of the sites were designated as landuse- index sites and were sampled as many as five additional times during the study. No samples exceeded state or federal drinking-water standards for chloride, sodium, nitrate, orthophosphate, herbicides, or herbicide degradates. The chemical composition of base-flow samples was classified into major-ion water types, which were broadly defined as naturally occurring and road-salt-affected water types. About one-third of the base-flow samples were roadsalt- affected types. Natural water types were differentiated as dilute or evolved. Dilute waters have bicarbonate and sulfate as dominant anions and evolved waters have only bicarbonate as a dominant anion. Dilute water types indicate relatively short ground-water residence times or contact with unreactive aquifer material. Evolved waters have either longer ground-water residence time or contact with more reactive aquifer material than dilute ground waters. The larger subbasins with wider valley-bottom areas were more likely to have evolved water types than small subbasins with little floodplain development. Positive correlations between selected constituents and the intensity of nonpoint sources emphasize the connection between land use, shallow ground-water quality, and stream base-flow water quality. Chloride and sodium, which are relatively conservative constituents, showed strong linear relations with annual estimates of road-salt application during all four sampling periods. Nonconservative constituents, such as the nutrients nitrate and orthophosphate, showed linear relations with manure production rate among farmed basins, but only at specific times of the year because of losses through biologic activity. Nitrate showed the strongest relation in winter because losses to biological activity were at a minimum. Orthophosphate showed the strongest relation in early summer, when hydrologic and chemical conditions appear to favor release from sediments. Atmospheric nitrogen deposition is an additional source of nitrogen that can be released from mature or stressed forested basins. Detections of herbicides (atrazine, metolachlor, simazine) and herbicide degradates ( Metolachlor ESA, alachlor ESA, deethylatrazine) in base flow were closely correlated with subbasins in which corn was grown during the study. Atrazine was detected at the farmed index site only in early summer, after application and two rain storms. This detection corresponded to the peak orthophosphate concentration. In contrast, metolachlor ESA was detected in nearly all farmedindex- subbasin samples and peaked in late summer, when percent base-flow contributions from farmed valley-bottom areas were likely highest. The implications of this study are that seasonal and more frequent base-flow surveys of water chemistry from small stream basins can help refine the understanding of local hydrogeologic systems and define the effects of nonpointsource contamination on base-flow water quality. The concentration of most nonpoint sources in valley-bottom or lower-hillside areas helped indicate the relative contributions of water from hillside and valley-bottom areas at different times of year. The positive correlations between the intensity of nonpoint-source activities and nonpoint-source constituents in base flow underscores the link between land use (nonpoint sources), ground-water quality, and surface-water quality.

Scientific Investigations Report↗
USGS2005

Use of tree-ring chemistry to document historical ground-water contamination events

The annual growth rings of tulip trees ( Liriodendron tulipifera L.) appear to preserve a chemical record of ground-water contamination at a landfill in Maryland. Zones of elevated iron and chlorine concentrations in growth rings from trees immediately downgradient from the landfill are closely correlated temporally with activities in the landfill expected to generate iron and chloride contamination in the ground water. Successively later iron peaks in trees increasingly distant from the landfill along the general direction of ground-water flow imply movement of iron-contaminated ground water away from the landfill. The historical velocity of iron movement (2 to 9 m/yr) and chloride movement (at least 40 m/yr) in ground water at the site was estimated from element-concentration trends of trees at successive distances from the landfill. The tree-ring-derived chloride-transport velocity approximates the known ground-water velocity (30 to 80 m/yr). A minimum horizontal hydraulic conductivity (0.01 to .02 cm/s) calculated from chloride velocity agrees well with values derived from aquifer tests (about 0.07 cm/s) and from ground-water modeling results (0.009 to 0.04 cm/s).

Groundwater↗
USGS2010

Hydrogeology and water quality of the Floridan aquifer system and effect of Lower Floridan aquifer pumping on the Upper Floridan aquifer at Hunter Army Airfield, Chatham County, Georgia

Test drilling and field investigations, conducted at Hunter Army Airfield (HAAF), Chatham County, Georgia, during 2009, were used to determine the geologic, hydraulic, and water-quality characteristics of the Floridan aquifer system and to evaluate the effect of Lower Floridan aquifer (LFA) pumping on the Upper Floridan aquifer (UFA). Field investigation activities included (1) constructing a 1,168-foot (ft) test boring and well completed in the LFA, (2) collecting drill cuttings and borehole geophysical logs, (3) collecting core samples for analysis of vertical hydraulic conductivity and porosity, (4) conducting flowmeter and packer tests in the open borehole within the UFA and LFA, (5) collecting depth-integrated water samples to assess basic ionic chemistry of various water-bearing zones, and (6) conducting aquifer tests in the new LFA well and in an existing UFA well to determine hydraulic properties and assess interaquifer leakage. Using data collected at the site and in nearby areas, model simulation was used to quantify the effects of interaquifer leakage on the UFA and to determine the amount of pumping reduction required in the UFA to offset drawdown resulting from the leakage. Borehole-geophysical and flowmeter data indicate the LFA at HAAF consists of limestone and dolomitic limestone between depths of 703 and 1,080 ft, producing water from six major permeable zones: 723-731; 768-785; 818-837; 917-923; 1,027-1,052; and 1,060-1,080 ft. Data from a flowmeter survey, conducted at a pumping rate of 748 gallons per minute (gal/min), suggest that the two uppermost zones contributed 469 gal/min or 62.6 percent of the total flow during the test. The remaining four zones contributed from 1.7 to 18 percent of the total flow. Grab water samples indicate that with the exception of fluoride, constituent concentrations in the LFA increased with depth; water from the deepest interval (1,075 ft) contained chloride and sulfate concentrations of 480 and 240 milligrams per liter (mg/L), respectively. These relatively high concentrations were interpreted to have little effect on the overall quality of the well because flowmeter results indicated that water from 1,060 to 1,080 ft contributed less than 2 percent of the total flow to the completed well. Results of a 72-hour aquifer test indicate that pumping a LFA well at a rate of 748 gal/min produced a drawdown response of 0.76 ft in a well completed in the UFA located 176 ft from the pumped well. A revised regional groundwater-flow model was used to simulate long-term (steady-state) leakage response of the UFA to pumping from the LFA and to estimate the equivalent amount of pumping from the UFA that would produce similar drawdown. Pumping the well at a rate of 748 gal/min (about 1 million gallons per day [Mgal/d]) resulted in a maximum simulated steady-state drawdown of 36.2 ft in the LFA and was greater than 1 ft over a 146 square-mile area. Simulated steady-state drawdown in the overlying UFA that resulted from interaquifer leakage was greater than 1 ft over a 141 square-mile area and was 2.03 ft at the pumped well. Flow to the pumped well was derived from increased lateral flow across the specified-head boundary (0.02 Mgal/d) and increased leakage from the UFA (0.52 Mgal/d), and by reductions in discharge to the Lower Floridan confining unit (0.53 Mgal/d) and to the lateral specified-head boundary (0.53 Mgal/d). Sixty-five percent of the leakage from the UFA occurred within 1 mile of the pumped well. This larger contribution results from a larger head gradient between the pumped well and the overlying aquifer in areas close to the pumped well. The Georgia Environmental Protection Division interim permitting strategy for the LFA requires simulation of (1) aquifer leakage from the UFA to LFA resulting from pumping the new LFA well, and (2) the equivalent rate of UFA pumping that induces the identical maximum drawdown in the UFA that would be expected as a result of pumping th

Georgia↗
USGS2011

Hydrogeology and water quality of the Floridan aquifer system and effects of Lower Floridan aquifer pumping on the Upper Floridan aquifer at Fort Stewart, Georgia

Test drilling, field investigations, and digital modeling were completed at Fort Stewart, GA, during 2009?2010, to assess the geologic, hydraulic, and water-quality characteristics of the Floridan aquifer system and evaluate the effect of Lower Floridan aquifer (LFA) pumping on the Upper Floridan aquifer (UFA). This work was performed pursuant to the Georgia Environmental Protection Division interim permitting strategy for new wells completed in the LFA that requires simulation to (1) quantify pumping-induced aquifer leakage from the UFA to LFA, and (2) identify the equivalent rate of UFA pumping that would produce the same maximum drawdown in the UFA that anticipated pumping from LFA well would induce. Field investigation activities included (1) constructing a 1,300-foot (ft) test boring and well completed in the LFA (well 33P028), (2) constructing an observation well in the UFA (well 33P029), (3) collecting drill cuttings and borehole geophysical logs, (4) collecting core samples for analysis of vertical hydraulic conductivity and porosity, (5) conducting flowmeter and packer tests in the open borehole within the UFA and LFA, (6) collecting depth-integrated water samples to assess basic ionic chemistry of various water-bearing zones, and (7) conducting aquifer tests in new LFA and UFA wells to determine hydraulic properties and assess interaquifer leakage. Using data collected at the site and in nearby areas, model simulation was used to assess the effects of LFA pumping on the UFA. Borehole-geophysical and flowmeter data indicate the LFA at Fort Stewart consists of limestone and dolomitic limestone between depths of 912 and 1,250 ft. Flowmeter data indicate the presence of three permeable zones at depth intervals of 912-947, 1,090-1,139, and 1,211?1,250 ft. LFA well 33P028 received 50 percent of the pumped volume from the uppermost permeable zone, and about 18 and 32 percent of the pumped volume from the middle and lowest permeable zones, respectively. Chemical constituent concentrations increased with depth, and water from all permeable zones contained sulfate at concentrations that exceeded the U.S. Environmental Protection Agency secondary maximum contaminant level of 250 milligrams per liter. A 72-hour aquifer test pumped LFA well 33P028 at 740 gallons per minute (gal/min), producing about 39 ft of drawdown in the pumped well and about 0.4 foot in nearby UFA well 33P029. Simulation using the U.S. Geological Survey finite-difference code MODFLOW was used to determine long-term, steady-state flow in the Floridan aquifer system, assuming the LFA well was pumped continuously at a rate of 740 gal/min. Simulated steady-state drawdown in the LFA was identical to that observed in pumped LFA well 33P028 at the end of the 72-hour test, with values larger than 1 ft extending 4.4 square miles symmetrically around the pumped well. Simulated steady-state drawdown in the UFA resulting from pumping in LFA well 33P028 exceeded 1 ft within a 1.4-square-mile circular area, and maximum drawdown in the UFA was 1.1 ft. Leakage from the UFA through the Lower Floridan confining unit contributed about 98 percent of the water to the well; lateral flow from specified-head model boundaries contributed about 2 percent. About 80 percent of the water supplied to LFA well 33P028 originated from within 1 mile of the well, and 49 percent was derived from within 0.5 mile of the well. Vertical hydraulic gradients and vertical leakage are progressively higher near the LFA pumped well which results in a correspondingly higher contribution of water from the UFA to the pumped well at distances closer to the pumped well. Simulated pumping-induced interaquifer leakage from the UFA to the LFA totaled 725 gal/min (1.04 million gallons per day), whereas simulated pumping at 205 gal/min (0.3 million gallons per day) from UFA well 33P029 produced the equivalent maximum drawdown as pumping LFA well 33P028 at 740 gal/min during the aquifer test. This equivalent pumpin

Georgia↗
USGS2000

A hydrologic primer for New Jersey watershed management

The U.S. Geological Survey (USGS) and the N.J. Department of Environmental Protection (NJDEP), and many other agencies and organizations are striving to educate the public about New Jersey&rsquo;s water resources. In 1996, the NJDEP began implementing a &ldquo;watershed management approach&rdquo; to maintain the physical, chemical, and biological integrity of New Jersey&rsquo;s waters. This approach concentrates on managing individual watershed areas by (1) defining the physical geographic boundaries of the watersheds, (2) basing water policy on sound scientific principles, and (3) developing partnerships with the public--the people most affected by watershed-management policies. New Jersey can be divided into five water regions as defined by the NJDEP: the Northeast, Raritan, Northwest, Lower Delaware, and Atlantic Coastal water regions (fig. 1). Each water region has been divided into three to five &ldquo;watershed-management areas,&rdquo; each of which encompasses a particular group of major rivers (fig. 2a-e). Each watershed management area consists of many smaller watersheds. Hydrologic data collected by Federal and State government agencies are invaluable as resources to policymakers who make decisions that affect the use of water in a particular watershed. The purpose of this report is to educate water-resource managers, policymakers, government officials, and the public about hydrologic concepts and the water-resource data needed to make informed decisions about water-management issues. (&ldquo;Hydrologic&rdquo; means relating to the occurrence, distribution, movement, and chemistry of all waters of the Earth (Fetter, 1980)). The first part of the report describes basic hydrologic concepts and includes explanations of the hydrologic cycle, the water budget, the surfacewater and ground-water flow systems, water-quality concepts and standards, and water use. The second part of the report summarizes the types of waterresource data that are available from Federal and State government agencies. Instructions on how to obtain the data and contact the appropriate Federal and State agencies, as well as suggestions for additional reading, also are included.

New Jersey↗
USGS1998

Chemistry and isotopic composition of ground water along a section near the Newmark area, San Bernardino County, California

Chemical and isotopic analyses and flow-meter measurements in pumped wells were used to determine the source, movement, and age of ground water along a section of the valley-fill aquifer from the San Jacinto Fault to the base of the San Bernardino Mountains near the Newmark area in the Bunker Hill Basin of southern California. Water samples were collected from four multiple-depth well sites, from different depths within three production wells, and from two nearby streams; these samples were analyzed for major ions, selected trace elements, stable isotopes of oxygen and hydrogen (delta oxygen-18 and delta deuterium), tritium, and carbon-14. Within the production wells, variations in vertical flowrate with depth were recorded during pumped conditions using a standard spinner tool. Where saturated, the upper 200 feet of unconsolidated deposits contributed as much as 60 percent of the well discharge; deposits at depths greater than 700 feet contributed less than 10 percent. Chemical analyses indicate that three general zones of ground-water quality are present along a north-south section--an oxygenated zone near the base of the San Bernardino Mountains, an oxygen-depleted zone near the San Jacinto Fault, and a deeper zone characterized by concentrations of fluoride greater than 1 mg/L and by a general water-quality composition similar to that of base flow in East Twin Creek. The presence of tritium in water from wells along the section indicates that post-1952 recharge has moved rapidly through the valley-fill aquifer to depths as great as 800 feet. Carbon-14 data indicate that the maximum age of ground water, sampled at depths ranging from 600 to 1,000 feet, is less than 5,000 years before present. Ground water along the study section is much younger than ground water from similar depths in other nearby basins. Delta oxygen-18 and delta deuterium data indicate that as much as 25 percent of the discharge from some wells near the base of the San Bernardino Mountains is water that was imported from northern California. Improved knowledge of depth-dependent ground-water flow along this section can aid in the design of an effective strategy for basin management, including remediation of the Newmark area, which is designated by the U.S. Environmental Protection Agency as a Superfund cleanup site.

Water-Resources Investigations Report↗
USGS1994

Effects of selective handling of pyritic, acid-forming materials on the chemistry of pore gas and ground water at a reclaimed surface coal mine in Clarion County, PA, USA

A change from dragline to “selective handling” mining methods at a reclaimed surface coal mine in western Pennsylvania did not significantly affect concentrations of metals in ground water because oxidation of pyrite and dissolution of siderite were not abated. Throughout the mine, placement of pyritic material near the land surface facilitated the oxidation of pyrite, causing the consumption of oxygen (O 2 ) and release of acid, iron, and sulfate ions. Locally in the unsaturated zone, water sampled within or near pyritic zones was acidic, with concentrations of sulfate exceeding 3,000 milligrams per liter (mg/L). However, acidic conditions generally did not persist below the water table because of neutralization by carbonate minerals. Dissolution of calcite, dolomite, and siderite in unsaturated and saturated zones produced elevated concentrations of carbon dioxide (CO 2 ), alkalinity, calcium, magnesium, iron, and manganese. Alkalinity concentrations of 600 to 800 mg/L as CaCO 3 were common in water samples from the unsaturated zone in spoil, and alkalinities of 100 to 400 mg/L as CaCO 3 were common in ground-water samples from the underlying saturated zone in spoil and bedrock. Saturation indices indicated that siderite could dissolve in water throughout the spoil, but that calcite dissolution or precipitation could occur locally. Calcite dissolution could be promoted as a result of pyrite oxidation, gypsum precipitation, and calcium ion exchange for sodium. Calcite precipitation could be promoted by evapotranspiration and siderite dissolution, and corresponding increases in concentrations of alkalinity and other solutes. Partial pressures of O 2 (Po 2 ) and CO 2 (Pco 2 ) in spoil pore gas indicated that oxidation of pyrite and precipitation of ferric hydroxide, coupled with dissolution of calcite, dolomite, and siderite were the primary reactions affecting water quality. Highest vertical gradients in Po 2 , particularly in the near-surface zone (0-1 m), did not correlate with concentrations of total sulfur in spoil. This lack of correlation could indicate that total sulfur concentrations in spoil do not reflect the amount of reactive pyrite or that oxidation rates can be controlled more by rates of O 2 diffusion than the amount of pyrite. Hence, if placed in O 2 -rich zones near the land surface, even small amounts of disseminated pyritic material can be relatively significant sources of acid and mineralized water.

Pennsylvania↗
USGS2019

Pallid sturgeon basin-wide contaminants assessment

Pallid sturgeon (Scaphirhynchus albus), listed as endangered in 1990 under the federal Endangered Species Act (United States Fish and Wildlife Service (USFWS), 1990), have declined due to habitat loss, commercial fishing, and hybridization. Pollution in the Missouri and Mississippi Rivers has to-date only received minor attention as a factor in the on-going decline of wild pallid sturgeon populations (Jacobson et al. 2016a; Bergman 2008). Pallid sturgeon experts and contaminant specialists conceived of the Pallid Sturgeon Basin-Wide Contaminants Assessment (Assessment) to identify potentially harmful contaminants (contaminants of concern), their distribution within pallid sturgeon habitat, and their effects on pallid sturgeon at the landscape level. Extant water quality and analytical chemistry data from samples of river water, sediment, and sturgeon tissues from past studies, assessments, or monitoring activities throughout the species’ range were used to establish a list of contaminants. The list includes: metal and non-metal elements, pesticides, organic industrial chemicals, hormones, nutrients, and other potential water quality contaminants. Environmental samples collected from January 1, 2001 through December 31, 2014, when available, were used for all evaluations. This report is effectively a screening level hazard assessment whereby contituents of concern that may pose a potential harm to pallid sturgeon have been identified. These constituents of concern warrant further examination to determine the level of risk they pose to pallid sturgeon. The Assessment process was one of comparing the existing environmental data for individual constituents to reference values for adverse effects on fish specifically or aquatic life generally. The product of the Assessment is a simplified summary that is geographically organized by pallid sturgeon management unit that generally categorizes each individual contaminant or water quality constituent according to operationally defined levels of concern. This hazard assessment identifies potential constituents of concern to pallid sturgeon and may support prioritization for future data collection and research to enable a quantitative risk assessment. Regional data density at spatial and temporal scales notwithstanding, the Assessment points to some generalities in contaminant concerns within and across management units. Metals but not pesticides are the predominant contaminant of concern in the Great Plains Management Unit (GPMU). In the Central Lowlands Management Unit (CLMU), selenium exceeds benchmark levels. Triazine herbicides are potentially of concern in all but the GPMU. Concentrations of legacy contaminants such as PCBs and DDT and its metabolites exceeded benchmarks in samples from the CLMU, Interior Highlands Mangement Unit (IHMU), and Coastal Plains Management Unit (CPMU), but local and national trends indicate environmental levels of these contaminants continue to decline. Observed concentrations of nutrients and indicators of nutrient pollution were above benchmark levels throughout the pallid sturgeon’s range; however, the significance for pallid sturgeon health specifically is unknown. Almost no information exists on contemporary contaminants of concern such as the natural and synthetic estrogens (estradiol, ethinyl estradiol, and estrone) or polybrominated diphenyls (PBDEs). There are considerable informational data gaps for contaminants throughout the species’ range. Water quality measurements were the most frequent data encountered whereas, sediment and tissue data were orders of magnitude less frequent. The paucity of sediment and tissue concentrations, particularly the latter, prevents any meaningful conclusions regarding adverse effects of these contaminants on the growth and reproduction of pallid sturgeon. However, the Assessment could form the basis for regional workshops with subject matter specialists to develop plans to evaluate the contaminants most likely to affect pallid sturgeon health.

Missouri River basin, Mississippi River basin↗
USGS2004

Variation in responses to spawning Pacific salmon among three south-eastern Alaska streams

1. Pacific salmon are thought to stimulate the productivity of the fresh waters in which they spawn by fertilising them with marine-derived nutrients (MDN). We compared the influence of salmon spawners on surface streamwater chemistry and benthic biota among three southeastern Alaska streams. Within each stream, reaches up- and downstream of barriers to salmon migration were sampled during or soon after spawners entered the streams. 2. Within streams, concentrations of dissolved ammonium and soluble reactive phosphorus (SRP), abundance of epilithon (chlorophyll a and ash-free dry mass) and biomass of chironomids were significantly higher in reaches with salmon spawners. In contrast, biomass of the mayflies Epeorus spp. and Rhithrogena spp. was significantly higher in reaches lacking spawners. 3. Among streams, significant differences were found in concentrations of dissolved ammonium, dissolved organic carbon, nitrate and SRP, abundance of epilithon, and the biomass of chironomids and Rhithrogena. These differences did not appear to reflect differences among streams in spawner density, nor the changes in water chemistry resulting from salmon spawners. 4. Our results suggest that the 'enrichment' effect of salmon spawners (e.g. increased streamwater nutrient concentrations) was balanced by other concurrent effects of spawners on streams (e.g. sediment disturbance). Furthermore, the collective effect of spawners on lotic ecosystems is likely to be constrained by conditions unique to individual streams, such as temperature, background water chemistry and light attenuation.

Freshwater Biology↗
USGS2006

Variability of isotope and major ion chemistry in the Allequash Basin, Wisconsin

As part of ongoing research conducted at one of the U.S. Geological Survey's Water, Energy, and Biogeochem-ical Budgets sites, work was undertaken to describe the spatial and temporal variability of stream and ground water isotopic composition and cation chemistry in the Trout Lake watershed, to relate the variability to the watershed flow system, and to identify the linkages of geochemical evolution and source of water in the watershed. The results are based on periodic sampling of sites at two scales along Allequash Creek, a small headwater stream in northern Wisconsin. Based on this sampling, there are distinct water isotopic and geochemical differences observed at a smaller hillslope scale and the larger Allequash Creek scale. The variability was larger than expected for this simple watershed, and is likely to be seen in more complex basins. Based on evidence from multiple isotopes and stream chemistry, the flow system arises from three main source waters (terrestrial-, lake-, or wetland-derived recharge) that can be identified along any flowpath using water isotopes together with geochemical characteristics such as iron concentrations. The ground water chemistry demonstrates considerable spatial variability that depends mainly on the flow-path length and water mobility through the aquifer. Calcium concentrations increase with increasing flowpath length, whereas strontium isotope ratios increase with increasing extent of stagnation in either the unsaturated or saturated zones as waters move from source to sink. The flowpath distribution we identify provides important constraints on the calibration of ground water flow models such as that undertaken by Pint et al. (this issue).

Wisconsin↗