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Hydrologic data for the Walker River Basin, Nevada and California, water years 2010–14

Walker Lake is a threatened and federally protected desert terminal lake in western Nevada. To help protect the desert terminal lake and the surrounding watershed, the Bureau of Reclamation and U.S. Geological Survey have been studying the hydrology of the Walker River Basin in Nevada and California since 2004. Hydrologic data collected for this study during water years 2010 through 2014 included groundwater levels, surface-water discharge, water chemistry, and meteorological data. Groundwater levels were measured in wells, and surface-water discharge was measured in streams, canals, and ditches. Water samples for chemical analyses were collected from wells, streams, springs, and Walker Lake. Chemical analyses included determining physical properties; the concentrations of major ions, nutrients, trace metals, dissolved gases, and radionuclides; and ratios of the stable isotopes of hydrogen and oxygen. Walker Lake water properties and meteorological parameters were monitored from a floating platform on the lake. Data collection methods followed established U.S. Geological Survey guidelines, and all data are stored in the National Water Information System database. All of the data are presented in this report and accessible on the internet, except multiple-depth Walker Lake water-chemistry data, which are available only in this report.

California, Nevada

Water-quality data for streams in the southern Yampa River basin, northwestern Colorado

Increases in coal mining in Colorado have raised questions regarding the impact of mining on the quality of surface water. An area where increases have caused particular concern is in northwestern Colorado, in the southern part of the Yampa River basin. In order to identify the changes produced by mining in the area it is necessary first to identify the water chemistry resulting from the geology, climate, and land use. To answer the above questions, a program for the synoptic collection of water-quality data was developed in which a network of sampling sites was established to determine the surface-water chemistry. This study was begun in April 1981. Water-quality samples were collected from sites on all continuously flowing streams in the southern part of the Yampa River basin from the Oak Creek drainage near Steamboat Springs on the east to the surface-water gaging station on the Yampa River near Maybell on the west. Each water-quality site was sampled repetitively as changes occurred in discharge and specific conductance. Water-quality data from surface-water gaging stations in the area for water years 1976 to 1981 are included in the report.

Open-File Report

Critical shifts in trace metal transport and remediation performance under future low river flows

Exceptionally low river flows are predicted to become more frequent and more severe across many global regions as a consequence of climate change. Investigations of trace metal transport dynamics across streamflows reveal stark changes in water chemistry, metal transformation processes, and remediation effectiveness under exceptionally low-flow conditions. High spatial resolution hydrological and water quality datasets indicate that metal-rich groundwater will exert a greater control on stream water chemistry and metal concentrations because of climate change. This is because the proportion of stream water sourced from mined areas and mineralized strata will increase under predicted future low-flow scenarios (from 25% under Q45 flow to 66% under Q99 flow in this study). However, mineral speciation modelling indicates that changes in stream pH and hydraulic conditions at low flow will decrease aqueous metal transport and increase sediment metal concentrations by enhancing metal sorption directly to streambed sediments. Solute transport modelling further demonstrates how increases in the importance of metal-rich diffuse groundwater sources at low flow could minimize the benefits of point source metal contamination treatment. Understanding metal transport dynamics under exceptionally low flows, as well as under high flows, is crucial to evaluate ecosystem service provision and remediation effectiveness in watersheds under future climate change scenarios.

Environmental Science & Technology

Determining long time-scale hyporheic zone flow paths in Antarctic streams

In the McMurdo Dry Valleys of Antarctica, glaciers are the source of meltwater during the austral summer, and the streams and adjacent hyporheic zones constitute the entire physical watershed; there are no hillslope processes in these systems. Hyporheic zones can extend several metres from each side of the stream, and are up to 70 cm deep, corresponding to a lateral cross‐section as large as 12 m 2 , and water resides in the subsurface year around. In this study, we differentiate between the near‐stream hyporheic zone, which can be characterized with stream tracer experiments, and the extended hyporheic zone, which has a longer time‐scale of exchange. We sampled stream water from Green Creek and from the adjacent saturated alluvium for stable isotopes of D and 18 O to assess the significance and extent of stream‐water exchange between the streams and extended hyporheic zones over long time‐scales (days to weeks). Our results show that water residing in the extended hyporheic zone is much more isotopically enriched (up to 11‰ D and 2·2‰ 18 O) than stream water. This result suggests a long residence time within the extended hyporheic zone, during which fractionation has occurred owing to summer evaporation and winter sublimation of hyporheic water. We found less enriched water in the extended hyporheic zone later in the flow season, suggesting that stream water may be exchanged into and out of this zone, on the time‐scale of weeks to months. The transient storage model OTIS was used to characterize the exchange of stream water with the extended hyporheic zone. Model results yield exchange rates (α) generally an order magnitude lower (10 −5 s −1 ) than those determined using stream‐tracer techniques on the same stream. In light of previous studies in these streams, these results suggest that the hyporheic zones in Antarctic streams have near‐stream zones of rapid stream‐water exchange, where ‘fast’ biogeochemical reactions may influence water chemistry, and extended hyporheic zones, in which slower biogeochemical reaction rates may affect stream‐water chemistry at longer time‐scales.

Hydrological Processes

Water-quality characteristics and trend analyses for the Tongue, Powder, Cheyenne, and Belle Fourche River drainage basins, Wyoming and Montana, for selected periods, water years 1991 through 2010

The Powder River structural basin in northeastern Wyoming and southeastern Montana is an area of ongoing coalbed natural gas (CBNG) development. Waters produced during CBNG development are managed with a variety of techniques, including surface impoundments and discharges into stream drainages. The interaction of CBNG-produced waters with the atmosphere and the semiarid soils of the Powder River structural basin can affect water chemistry in several ways. Specific conductance and sodium adsorption ratios (SAR) of CBNG-produced waters that are discharged to streams have been of particular concern because they have the potential to affect the use of the water for irrigation. Water-quality monitoring has been conducted since 2001 at main-stem and tributary sites in the Tongue, Powder, Cheyenne, and Belle Fourche River drainage basins in response to concerns about CBNG effects. A study was conducted to summarize characteristics of stream-water quality for water years 2001–10 (October 1, 2000, to September 30, 2010) and examine trends in specific conductance, SAR, and primary constituents that contribute to specific conductance and SAR for changes through time (water years 1991–2010) that may have occurred as a result of CBNG development. Specific conductance and SAR are the focus characteristics of this report. Dissolved calcium, magnesium, and sodium, which are primary contributors to specific conductance and SAR, as well as dissolved alkalinity, chloride, and sulfate, which are other primary contributors to specific conductance, also are described. Stream-water quality in the Tongue, Powder, Cheyenne, and Belle Fourche River drainage basins was variable during water years 2001–10, in part because of variations in streamflow. In general, annual runoff was less than average during water years 2001–06 and near or above average during water years 2007–10. Stream water of the Tongue River had the smallest specific conductance values, sodium adsorption ratios, and major ion concentrations of the main-stem streams. Sites in the Tongue River drainage basin typically had the smallest range of specific conductance and SAR values. The water chemistry of sites in the Powder River drainage basin generally was the most variable as a result of diverse characteristics of that basin. Plains tributaries in the Powder River drainage basin had the largest range of specific conductance and SAR values, in part due to the many tributaries that receive CBNG-produced waters. Trends were analyzed using the seasonal Kendall test with flow-adjusted concentrations to determine changes to water quality through time at sites in the Tongue, Powder, Cheyenne, and Belle Fourche River drainage basins. Trends were evaluated for water years 2001–10 for 17 sites, which generally were on the main-stem streams and primary tributaries. Trends were evaluated for water years 2005–10 for 26 sites to increase the spatial coverage of sites. Trends were evaluated for water years 1991–2010 for eight sites to include water-quality data collected prior to widespread CBNG development and expand the temporal context of trends. Consistent patterns were not observed in trend results for water years 2001–10 for flow-adjusted specific conductance and SAR values in the Tongue, Powder, and Belle Fourche River drainage basins. Significant (p-values less than 0.05) upward trends in flow-adjusted specific conductance values were determined for 3 sites, a downward trend was determined for 1 site, and no significant (p-value greater than 0.05) trends were determined for 13 sites. One of the sites with a significant upward trend was the Tongue River at the Wyoming-Montana State line. No trend in flow-adjusted specific conductance values was determined for the Powder River at Moorhead, Mont. Significant upward trends in flow-adjusted SAR values were determined for 2 sites and no significant trends were determined for 15 sites. No trends in flow-adjusted SAR values were determined for the Tongue River at the Wyoming-Montana State line or for the Powder River at Moorhead, Mont. One of the sites with a significant upward trend in flow-adjusted SAR values was the Powder River at Arvada, Wyo. For water years 2005–10, significant upward trends in flow-adjusted specific conductance values were determined no significant trends were determined for 13 sites. A significant upward trend was determined for flow-adjusted specific conductance values for the Tongue River at the Wyoming-Montana State line. No trend in flow-adjusted specific conductance values was determined for the Powder River at Moorhead, Mont. Significant upward trends in flow-adjusted SAR values were determined for 4 sites, downward trends were determined for 5 sites, and no significant trend was determined for 17 sites. No trends in flow-adjusted SAR values were determined for the Tongue River at the Wyoming-Montana State line or for the Powder River at Moorhead, Mont. Results of the seasonal Kendall test applied to flow-adjusted specific conductance values for water years 1991–2010 indicated no significant trend for eight sites in the Tongue, Powder, and Belle Fourche River drainage basins. No significant trend in flow-adjusted specific conductance was determined for the Tongue River at the Wyoming-Montana State line or the Powder River at Moorhead, Mont. Results of the seasonal Kendall test applied to flow-adjusted SAR values for water years 1991–2010 indicated an upward trend for one site and no significant trend for four sites in the Powder and Belle Fourche River drainage basins. The significant upward trend in flow-adjusted SAR values was determined for the Powder River at Arvada, Wyo., for water years 1991–2010. Results indicate that CBNG development in the Powder River structural basin may have contributed to some trends, such as the upward trend in flow-adjusted SAR for the Powder River at Arvada, Wyo., for water years 1991–2010. An upward trend in flow-adjusted alkalinity concentrations for water years 2001–10 also was determined for the Powder River at Arvada, Wyo. Trend results are consistent with changes that can occur from the addition of sodium and bicarbonate associated with CBNG-produced waters to the Powder River. Upward trends in constituents at other sites, including the Belle Fourche River, may be the result of declining CBNG development, indicating that CBNG-produced waters may have had a dilution effect on some streams. The factors affecting other trends could not be determined because multiple factors could have been affecting the stream-water quality or because trends were observed at sites upstream from CBNG development that may have affected water-quality trends at sites downstream.

Wyoming;Montana

The isometric log-ratio (ilr)-ion plot: A proposed alternative to the Piper diagram

The Piper diagram has been a staple for the analysis of water chemistry data since its introduction in 1944. It was conceived to be a method for water classification, determination of potential water mixing between end-members, and to aid in the identification of chemical reactions controlling a sample set. This study uses the information gleaned over the years since the release of the Piper diagram and proposes an alternative to it, capturing the strengths of the original diagram while adding new ideas to increase its robustness. The new method uses compositional data analysis to create 4 isometric log-ratio coordinates for the 6 major chemical species analyzed in the Piper diagram and transforms the data to a 4-field bi-plot, the ilr-ion plot. This ilr-ion plot conveys all of the information in the Piper diagram (water mixing, water types, and chemical reactions) while also visualizing additional data, the ability to examine Ca 2+ /Mg 2+ versus Cl-/SO 4 2− . The Piper and the ilr-ion plot were also compared using multiple synthetic and real datasets in order to illustrate the caveats and the advantages of using either diagram to analyze water chemistry data. Although there are challenges with using the ilr-ion plot (e.g., missing or zero values zeros in the dataset must be imputed by positive real numbers), it appears that the use of compositional data analysis coupled with the ilr-ion plot provides a more in-depth and complete analysis of water quality data compared to the original Piper diagram.

Journal of Geochemical Exploration

Subsurface water piping prevents meromixis in a deep volcanic crater lake (Dominica, West Indies)

Boeri Lake—a small (3.6 ha) but deep (39.6 m) crater lake on Morne Micotrin in Dominica, West Indies—presents a limnological enigma; it exhibits strong morphometric and circumstantial evidence for meromixis, yet it is not stratified. We tested the hypothesis that water seepage from Boeri Lake overcomes morphometric drivers of stratification and prevents the onset of meromixis. We compared water chemistry and plankton community composition in Boeri Lake to perennial streams on Morne Micotrin to assess if water discharging from these springs originates in Boeri Lake. Lacustrine phytoplankton and zooplankton taxa were detected in nearby streams, which also had similar water chemistry to Boeri Lake. In contrast, two other streams that drain Morne Micotrin and one neighboring reference stream had little in common with waters from Boeri Lake. This suggests that Boeri Lake’s anomalous limnology is explained by hydrologic connectivity to nearby flanking streams, and supports our hypothesis that subsurface water piping, combined with high annual rainfall, stymies the onset of meromixis. We provide an explanation for how holomictic lakes can persist and transport organisms through the ground in tropical mountain ecosystems and discuss implications of consistent water piping for plankton community assembly on island lakes.

Hydrobiologia

Changes in stream chemistry and nutrient export following a partial harvest in the Catskill Mountains, New York, USA

Clearcut forest harvesting typically results in large changes in stream water chemistry in northeastern North America. The effects of partial forest harvests on stream chemistry have not received as much attention, even though partial cutting is a more common forestry practice than clearcutting in this region. Changes in stream water chemistry following a partial cut are reported here from a 10 ha study catchment in a northern hardwood forest in the Catskill Mountains of southern New York, and are compared to those of a nearby 48 ha reference catchment. The lower two thirds of the treatment catchment was harvested in February-April 2002 by a shelterwood method, such that 33% of the basal area of the catchment was removed. Stream NO3-, NH4+, Ca2+, K+, and total dissolved aluminum (Alto) concentrations increased significantly after the harvest. Stream Ca2+, Mg2+ and NH4+ concentrations peaked 5 months after the initiation of the harvest, NO 3- and K+ concentrations peaked 6 months after cutting, and Alto concentrations peaked 1 year after cutting. Streamflow was not significantly affected by the harvest when compared to the flow of three nearby streams. Export of NO3- in stream water increased five-fold the year after the cut, and briefly exceeded atmospheric inputs of inorganic nitrogen during 4 months in the fall of 2002. Changes in stream NO3- and K+ concentrations were less than predicted by the relative basal area removed compared with those of a recent nearby clearcut. In contrast, changes in Ca2+, Mg 2+ and Alto concentrations were approximately proportional to basal area removal in these two cuts. Stream chemistry returned to values close to those of the pre-cut period and to reference values by early spring of 2003, just over a year after the initiation of the harvest, except for NO 3- concentrations, which remained elevated above background 18-20 months after completion of the cut.

Forest Ecology and Management

Geohydrology of a deep-aquifer system monitoring-well site at Marina, Monterey County, California

In 2000, a deep-aquifer system monitoring-well site (DMW1) was completed at Marina, California to provide basic geologic and hydrologic information about the deep-aquifer system in the coastal region of the Salinas Valley. The monitoring-well site contains four wells in a single borehole; one completed from 930 to 950 feet below land surface (bls) in the Paso Robles Formation (DMW1-4); one 1,040 to 1,060 feet below land surface in the upper Purisima Formation (DMW1-3); one from 1,410 to 1,430 feet below land surface in the middle Purisima Formation (DMW1-2); and one from 1,820 to 1,860 feet below land surface in the lower Purisima Formation (DMW1-1). The monitoring site is installed between the coast and several deep-aquifer system supply wells in the Marina Coast Water District, and the completion depths are within the zones screened in those supply wells. Sediments below a depth of 955 feet at DMW1 are Pliocene age, whereas the sediments encountered at the water-supply wells are Pleistocene age at an equivalent depth. Water levels are below sea level in DMW1 and the Marina Water District deep-aquifer system supply wells, which indicate that the potential for seawater intrusion exists in the deep-aquifer system. If the aquifers at DMW1 are hydraulically connected with the submarine outcrops in Monterey Bay, then the water levels at the DMW1 site are 8 to 27 feet below the level necessary to prevent seawater intrusion. Numerous thick fine-grained interbeds and confining units in the aquifer systems retard the vertical movement of fresh and saline ground water between aquifers and restrict the movement of seawater to narrow water-bearing zones in the upper-aquifer system.Hydraulic testing of the DMW1 and the Marina Water District supply wells indicates that the tested zones within the deep-aquifer system are transmissive water-bearing units with hydraulic conductivities ranging from 2 to 14.5 feet per day. The hydraulic properties of the supply wells and monitoring wells are similar, even though the wells are completed in different geologic formations.Geophysical logs collected at the DMW1 site indicate saline water in most water-bearing zones shallower than 720 feet below land surface and from about 1,025 to 1,130 feet below land surface, and indicate fresher water from about 910 to 950 feet below land surface (DMW1-4), 1,130 to 1,550 feet below land surface, and below 1,650 feet below land surface. Temporal differences between electromagnetic induction logs indicate possible seasonal seawater intrusion in five water-bearing zones from 350 to 675 feet below land surface in the upper-aquifer system.The water-chemistry analyses from the deep-aquifer system monitoring and supply wells indicate that these deep aquifers in the Marina area contain potable water with the exception of the saline water in well DMW1-3. The saline water from well DMW1-3 has a chloride concentration of 10,800 milligrams per liter and dissolved solids concentration of 23,800 milligrams per liter. The source of this water was determined not to be recent seawater based on geochemical indicators and the age of the ground water. The high salinity of this ground water may be related to the dissolution of salts from the saline marine clays that surround the water-bearing zone screened by DMW1-3. The major ion water chemistry of the monitoring wells and the nearby MCWD water-supply wells are similar, which may indicate they are in hydraulic connection, even though the stratigraphic layers differ below 955 feet below land surface.No tritium was detected in samples from the deep monitoring wells. The lack of tritium suggest that there is no recent recharge water (less than 50 years old) in the deep-aquifer system at the DMW1 site. The carbon-14 analyses of these samples indicate ground water from the monitoring site was recharged thousands of years ago.

California

Simulated effects of ground-water augmentation on the hydrology of Round and Halfmoon Lakes in northwestern Hillsborough County, Florida

Pumpage from the Upper Floridan aquifer in northwest Hillsborough County near Tampa, Florida, has induced downward leakage from the overlying surficial aquifer and lowered the water table in many areas. Leakage is highest where the confining layer separating the aquifers is breached, which is common beneath many of the lakes in the study area. Leakage of water to the Upper Floridan aquifer has lowered the water level in many lakes and drained many wetlands. Ground water from the Upper Floridan aquifer has been added (augmented) to some lakes in an effort to maintain lake levels, but the resulting lake-water chemistry and lake leakage patterns are substantially different from those of natural lakes. Changes in lake-water chemistry can cause changes in lake flora, fauna, and lake sediment composition, and large volumes of lake leakage are suspected to enhance the formation of sinkholes near the shoreline of augmented lakes. The leakage rate of lake water through the surficial aquifer to the Upper Floridan aquifer was estimated in this study using ground-water-flow models developed for an augmented lake (Round Lake) and non-augmented lake (Halfmoon Lake). Flow models developed with MODFLOW were calibrated through nonlinear regression with UCODE to measured water levels and monthly net ground-water-flow rates from the lakes estimated from lake-water budgets. Monthly estimates of ground-water recharge were computed using an unsaturated flow model (LEACHM) that simulated daily changes in storage of water in the soil profile, thus estimating recharge as drainage to the water table. Aquifer properties in the Round Lake model were estimated through transient-state simulations using two sets of monthly recharge rates computed during July 1996 to February 1999, which spanned both average conditions (July 1996 through October 1997), and an El Niño event (November 1997 through September 1998) when the recharge rate doubled. Aquifer properties in the Halfmoon Lake model were estimated through steady-state simulations of average conditions in July 1996. Simulated hydrographs computed by the Round and Halfmoon Lake models closely matched measured water-level fluctuations, except during El Niño, when the Halfmoon Lake model was unable to accurately reproduce water levels. Possibly, potential recharge during El Niño was diverted through ground-water-flow outlets that were not represented in the Halfmoon Lake model, or a large part of the rainfall was diverted into runoff before it could become recharge. Solute transport simulations with MT3D indicate that leakage of lake water extended 250 to 400 feet into the surficial aquifer around Round Lake, and from 75 to 150 feet around Halfmoon Lake before flowing to the underlying Upper Floridan aquifer. These results are in agreement with concentrations of stable isotopes of oxygen-18 (d18O) and deuterium (dD) in the surficial aquifer. Schedules of monthly augmentation rates to maintain constant stages in Round and Halfmoon Lakes were computed using an equation that accounted for changes in the Upper Floridan aquifer head and the deviation from the mean recharge rate. Resulting lake stages were nearly constant during the first half of the study, but increased above target lake stages during El Niño; modifying the computation of augmentation rates to account for the higher recharge rate during El Niño resulted in lake stages that were closer to the target lake stage. Substantially more lake leakage flows to the Upper Floridan aquifer from Round Lake than from Halfmoon Lake, because the estimated vertical hydraulic conductivities of lake and confining layer sediments and breaches in the confining layer beneath Round Lake are much greater. Augmentation rates required to maintain the low guidance stages in Round Lake (53 feet) and Halfmoon Lake (42 feet) under average Upper Floridan aquifer heads are estimated as 33,850 cubic feet per day and 1,330 to 10,000 cubic feet per day, respectively. These rates equate to 26 inches per month of water applied to the entire surface of Round Lake and 0.34 to 2.5 inches per month of water applied to Halfmoon Lake.

Florida

Hydrogeologic framework, ground-water geochemistry, and assessment of nitrogen yield from base flow in two agricultural watersheds, Kent County, Maryland

Hydrostratigraphic and geochemical data collected in two adjacent watersheds on the Delmarva Peninsula, in Kent County, Maryland, indicate that shallow subsurface stratigraphy is an important factor that affects the concentrations of nitrogen in ground water discharging as stream base flow. The flux of nitrogen from shallow aquifers can contribute substantially to the eutrophication of streams and estuaries, degrading water quality and aquatic habitats. The information presented in this report includes a hydrostratigraphic framework for the Locust Grove study area, analyses and interpretation of ground-water chemistry, and an analysis of nutrient yields from stream base flow. An understanding of the processes by which ground-water nitrogen discharges to streams is important for optimal management of nutrients in watersheds in which ground-water discharge is an appreciable percentage of total streamflow. The U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency (USEPA), collected and analyzed hydrostratigraphic and geochemical data in support of ground-water flow modeling by the USEPA. The adjacent watersheds of Morgan Creek and Chesterville Branch have similar topography and land use; however, reported nitrogen concentrations are generally 6 to 10 milligrams per liter in Chesterville Branch but only 2 to 4 milligrams per liter in Morgan Creek. Ground water in the surficial aquifer in the recharge areas of both streams has high concentrations of nitrate (greater than 10 milligrams per liter as N) and dissolved oxygen. One component of the ground water discharging to Morgan Creek typically is anoxic and contains virtually no dissolved nitrate; most of the ground water discharging to Chesterville Branch is oxygenated and contains moderately high concentrations of nitrate. The surficial aquifer in the study area is composed of the deeply weathered sands and gravels of the Pensauken Formation (the Columbia aquifer) and the underlying glauconitic sands of the upper Aquia Formation (the Aquia aquifer). The lower 6 to 9 meters of the Aquia Formation is a low-permeability silt-clay with abundant glauconite. The Aquia confining layer underlies the Columbia-Aquia surficial aquifer throughout the study area. The sediment redox transition, identified in cores, that occurs in the upper 0.5 to 1 meter of the Aquia confining layer is thought to be a site for subsurface denitrification of ground water. The first confined aquifer is composed of the glauconitic sands in the upper 9 to 11 meters of the Hornerstown Formation. The Hornerstown aquifer is underlain by 10 to 15 meters of glauconitic silt-clay at the base of the Hornerstown Formation (the Hornerstown confining layer), and 5 meters of low-permeability clay in the underlying Severn Formation. The Aquia and Hornerstown Formations dip and thicken to the southeast, and the Aquia confining layer subcrops shallowly (within 5 meters of the land surface) in a band that strikes southwest to northeast across the northern edge of the study area. The surficial aquifer is very thin (generally less than 5 meters) north of Morgan Creek, and the alluvial valley of Morgan Creek has incised into the top of the Aquia confining layer. In contrast, the Aquia confining layer lies 22 meters below Chesterville Branch, and the surficial aquifer approaches 30 meters in thickness (away from the creek). Chemically reduced iron sulfides and glauconite in the Aquia confining layer are likely substrates for denitrification of nitrate in ground water. Evidence from the dissolved concentrations of nitrate, sulfate, iron, argon, and nitrogen gas, and stable nitrogen isotopes support the interpretation that ground water flowing near the top of the Aquia confining layer, or through the confined Hornerstown aquifer, has undergone denitrification. This process appears to have the greatest effect on ground-water chemistry north of Morgan Creek, where the surficial aquifer is thin and a greater percentage of the ground water contacts the Aquia confining layer. The base-flow discharges of total nitrogen from the two watersheds are of similar magnitude, although Chesterville Branch has somewhat higher loads (29,000 kilograms of nitrogen per year) than Morgan Creek (20,000 kilograms of nitrogen per year), although Morgan Creek has a larger drainage area and a greater discharge of water. The base-flow yield of nitrogen (load per unit area) in Chesterville Branch (median of 0.058 grams per second per square kilometer at the outlet) is more than twice that of Morgan Creek (median of 0.022 grams per second per square kilometer at the outlet), reflecting the higher concentration of nitrate in ground water discharging to Chesterville Branch. Total nitrogen concentrations tend to decrease downstream in Chesterville Branch and increase downstream in Morgan Creek. The downstream trend in Chesterville Branch may be affected by instream nitrogen uptake and denitrification, and an increasing proportion of older, denitrified ground water in downstream discharge. The downstream trends in Morgan Creek may be affected by inflow from tributaries, downstream changes in the source of discharge water, and downstream changes in the riparian zone, which could affect the processes and degree of denitrification. Although these two watersheds appear to have landscape features (such as topography, land use, and soils) that would produce similar nitrogen discharges, a more detailed examination of landscape features indicates that Chesterville Branch has soils that are slightly better drained, tributary stream outlets at higher altitudes, and a slightly higher percentage of agricultural land. All of these factors have been related to higher nitrogen yields. Nonetheless, most of the data support the interpretation that hydrostratigraphy has the greatest effect in producing the difference in nitrogen yields between the two watersheds.

Maryland

Quality of water and chemistry of bottom sediment in the Rillito Creek basin, Tucson, Arizona, 1992-93

Physical and chemical data were collected from four surface-water sites, six ground-water sites, and two bottom-sediment sites during 1992-93. Specific conductance, hardness, alkalinity, and dissolved- solids concentrations generally were higher in ground water than in surface water. The median concentrations of dissolved major ions, with the exception of potassium, were higher in ground water than in surface water. In surface water and ground water, calcium was the dominant cation, and bicarbonate was the dominant anion. Concentrations of dissolved nitrite and nitrite plus nitrate in surface water and ground water did not exceed the U.S. Environmental Protection Agency maximum contaminant levels of 1 and 10 milligrams per liter for drinking water, respectively. Ammonium plus organic nitrogen in bottom sediment was detected at the highest concentration of any nitrogen species. Median values for most of the dissolved trace elements in surface water and ground water were below the detection levels. Dissolved trace elements in surface water and ground water did not exceed the U.S. Environmental Protection Agency maximum contaminant levels for drinking water. Trace-element concentrations in bottom sediment were similar to trace-element concentrations reported for soils of the western conterminous United States. Several organochlorine pesticides and priority pollutants were detected in surface-water and bottom-sediment samples; however, they did not exceed water-quality standards. Pesticides or priority pollutants were not detected in ground-water samples.

Water-Resources Investigations Report

Relation of hydrogeologic characteristics to distribution of radioactivity in ground water, Newark Basin, New Jersey

The distribution of radioactivity in ground water in the Newark Basin is controlled by the lithology of the aquifer and the degree of contact between the water that flows through the fractured strata and the radioactive lithologic units. The primary water-bearing lithologic units of the Newark Basin that contain elevated levels of radioactivity are the arkosic sandstones of the Stockton Formation and the black mudstones of the lower part of the Passaic Formation. Lithologic and hydrogeologic characteristics of these rock aquifers that affect the spatial distribution of radionuclides in the water include the concentration of radioactive minerals in the strata; the continuity of radioactive strata; the orientation, depth, interconnectedness, and continuity of regional and local fracture patterns; and the geochemical environment, which affects radionuclide solubility. The stratigraphic zones of uranium enrichment and the continuity of the radioactive strata differ between the Stockton Formation and the lower part of the Passaic Formation. Uranium enrichment in both formations, however, is identified in permeable sections of strata that have sharp contacts with, or that are enclosed by, less permeable zones. In the Stockton Formation, basal conglomerates overlying fine-grained mudstones are the most radioactive lithology. In interbedded red and black mudstones of the lower part of the Passaic Formation, the uranium-rich zones are the black and white carbonate-rich siltstone and mudstone laminae overlying massive fine-grained mudstones. Most samples of the arkosic sandstones of the Stockton Formation tended to be slightly enriched in uranium relative to thorium, whereas all samples of the black mudstones of the lower part of the Passaic Formation were heavily enriched in uranium with respect to thorium, with a maximum concentration of uranium of 6,200 parts per million (ppm). Spatial orientation of radioactive zones is controlled by the depositional environment of the host lithology. Radioactive strata in the arkosic sandstones of the Stockton Formation, which is deltaic or fluvial/deltaic in origin, arc stratigraphically discontinuous and nonplanar. In contrast, the radioactive lacustrine black mudstones of the lower part of the Passaic Formation are laterally continuous and planar. Geophysical logs of boreholes indicate that the number and depths of probable waterbearing fractures are greater in the arkoses of the Stockton Formation and red mudstones of the lower part of the Passaic Formation than in the interbedded red and black mudstones of the lower part of the Passaic Formation, despite the fact that fracture-density counts in cores indicate that black mudstones are more highly fractured than the other rock types. The total number of fractures is greater and bedding-plane fractures are generally more common in the lower part of the Passaic Formation than in the Stockton Formation. Fractures in the Stockton Formation form a well-connected network consisting of both bedding-plane and several sets of high-angle fractures present on a regional scale. The large-scale continuity of interconnected bedding-plane fractures and high-angle regional fractures may be partly responsible for the higher yields observed for wells in the Stockton Formation than for wells in the Passaic Formation and may facilitate migration of dissolved radionuclides far from their source. The well-connected fracture network may increase the likelihood that circulating water comes in contact with radioactive strata. Water in the black mudstones of the lower part of the Passaic Formation may also contain high levels of radioactivity, primarily as a result of the high frequency of radioactive strata and of fracturing, rather than the presence of a well-connected regional fracture system. Ground-water chemistry is dominated by the calcium cation and the bicarbonate anion, both derived from abundant secondary calcite in the fractures. The concentrations of uranium and radium in water that comes into contact with radioactive rock are controlled by the water chemistry. Uranium is the dominant alpha emitter in the oxidizing waters in the red mudstones of the Passaic Formation, whereas radium-226 (226Ra) is the dominant alpha emitter in the suboxic (reducing) water in the black mudstones of the lower part of the Passaic Formation. Because the lithology of the Stockton Formation and, in places, the lower part of the Passaic Formation varies greatly, wells can intercept multiple fracture zones that can contain oxic or suboxic waters, thereby resulting in the presence of both uranium and radium in detectable quantities in the same water sample.

New Jersey

Using bioavailability modeling to refine copper treatments for zebra mussel control and better understanding risks to non-target species

Copper can be toxic to aquatic organisms at high concentrations and has been previously used successfully to control zebra mussels ( Dreissena polymorpha ). Because copper’s toxicity changes with water chemistry, using the same copper concentration in different waterbodies could yield different outcomes. We demonstrate how measuring water chemistry parameters and using the Biotic Ligand Model (BLM) and multiple linear regression (MLR) models can predict a suitable, site-specific copper concentration for management. We exposed zebra mussel adults and non-target organisms to varying concentrations of copper over 10 d in a mobile laboratory. We found that one non-target species, Daphnia magna , had a 50% chance of survival at 9.50 µg Cu/L (i.e., the 50% lethal concentration, LC 50 ), within our BLM-predicted range of 3.38–16.95 µg Cu/L LC 50 values. In the future, managers could make similar predictions and tailor their copper concentrations to their management goals. We also measured zebra mussel larvae mortality at copper concentrations ranging from 0 to 191 µg Cu/L. While those results were inconclusive, we present the results of this work as a foundation for future projects. Our study underscores the importance of developing site-specific copper concentration recommendations and demonstrates the potential utility of the BLM and MLR approaches for informing those recommendations.

Minnesota

Transient hydrogeological controls on the chemistry of a seepage lake

A solute mass balance method was used to estimate groundwater inflow and outflow rates for Nevins Lake, Michigan, a seepage lake in the upper peninsula that historically has shown extremely variable water chemistry compared with most other seepage lakes. A 4-year study (1989–1992) of the hydrology and geochemistry of Nevins Lake and its contiguous groundwater system revealed that changes in the mass of dissolved solutes are the result of annual hydraulic gradient reversals. A pronounced acidification of Nevins Lake from 1986 to 1988 was likely caused by drought-induced diminished groundwater inflow rates. In this study, dissolved calcium (the major cation in water of Nevins Lake, groundwater, and precipitation) was used for estimating mass flow rates. During the 1989–1992 period, Nevins Lake showed a reproducible annual cycle in calcium mass. Immediately following spring snowmelt and the resulting hydraulic gradient reversal, the mass of dissolved calcium in the lake increases rapidly, and then it decreases steadily throughout the summer and early fall, at which time the lake becomes hydraulically mounded and receives no groundwater inflow. Groundwater flow rates estimated by the solute mass balance method are sensitive to assumed solute concentrations in discharging groundwater. Pore water samples from the lake bed are shown to be more representative of water discharging to the lake than are samples from piezometers near the lake shore, but spatial and temporal variability in pore water chemistry must be considered. Stable isotope analyses ( 18 O and 2 H) of lake water, groundwater, and pore water samples show that water discharging to Nevins Lake in the spring is entirely recycled lake water, and no groundwater derived from terrestrial recharge reaches the lake. The conceptual model formulated during this study linking lake chemistry and the contiguous groundwater system and general groundwater flow patterns surrounding highly transient lake systems are likely transferable to other similar systems.

Michigan

Response of fish assemblages to declining acidic deposition in Adirondack Mountain lakes, 1984–2012

Adverse effects of acidic deposition on the chemistry and fish communities were evident in Adirondack Mountain lakes during the 1980s and 1990s. Fish assemblages and water chemistry in 43 Adirondack Long-Term Monitoring (ALTM) lakes were sampled by the Adirondack Lakes Survey Corporation and the New York State Department of Environmental Conservation during three periods (1984–87, 1994–2005, and 2008–12) to document regional impacts and potential biological recovery associated with the 1990 amendments to the 1963 Clean Air Act (CAA). We assessed standardized data from 43 lakes sampled during the three periods to quantify the response of fish-community richness, total fish abundance, and brook trout ( Salvelinus fontinalis) abundance to declining acidity that resulted from changes in U.S. air-quality management between 1984 and 2012. During the 28-year period, mean acid neutralizing capacity (ANC) increased significantly from 3 to 30 μeq/L and mean inorganic monomeric Al concentrations decreased significantly from 2.22 to 0.66 μmol/L, yet mean species richness, all species or total catch per net night (CPNN), and brook trout CPNN did not change significantly in the 43 lakes. Regression analyses indicate that fishery metrics were not directly related to the degree of chemical recovery and that brook trout CPNN may actually have declined with increasing ANC. While the richness of fish communities increased with increasing ANC as anticipated in several Adirondack lakes, observed improvements in water quality associated with the CAA have generally failed to produce detectable shifts in fish assemblages within a large number of ALTM lakes. Additional time may simply be needed for biological recovery to progress, or else more proactive efforts may be necessary to restore natural fish assemblages in Adirondack lakes in which water chemistry is steadily recovering from acidification.

New York

Hydrology and geochemistry of a surface coal mine in northwestern Colorado

The hydrology and geochemistry of a reclaimed coal mine in northwestern Colorado were monitored during water years 1988 and 1989. Some data also were collected in water years 1987 and 1990. This report describes (1) the sources of hydrologic recharge to and discharge from reclaimed spoil, (2) the relative contributions of recharge to the reclaimed spoil aquifer from identified source waters and the rate of water movement from those sources to the reclaimed spoil, and (3) the geochemical reactions that control water quality in reclaimed spoil. The study area was at a dip-slope coal mine encompassing about 7 square miles with land slopes of varying aspect. The area was instrumented and monitored at five sites; two sites had unmined and reclaimed- spoil areas adjacent to each other and three sites were unmined. The mined areas had been reclaimed. Instrumentation at the study sites included 1 climate station, 3 rain gages, 19 soil-water access tubes, 2 lysimeters, 18 wells completed in bedrock, 7 wells completed in reclaimed spoil, and 2 surface- water gaging stations. The results of the study indicate that the reclaimed spoil is recharged from surface recharge and underburden aquifers. Discharge, as measured by lysimeters, was about 3 inches per year and occurred during and after snowmelt. Hydraulic-head measurements indicated a potential for ground-water movement from deeper to shallower aquifers. Water levels rose in the reclaimed-spoil aquifer and spring discharge at the toe of the spoil slopes increased rapidly in response to snowmelt. Water chemistry, stable isotopes, geochemical models, and mass-balance calculations indicate that surface recharge and the underburden aquifers each contribute about 50 percent of the water to the reclaimed-spoil aquifers. Geochemical information indicates that pyrite oxidation and dissolution of carbonate and efflorescent sulfate minerals control the water chemistry of the reclaimed-spoil aquifer.

Water-Resources Investigations Report

Diatom (Bacillariophyta) community response to water quality and land use

Aquatic algal communities are sensitive to environmental stresses and are used as indicators of water quality. Diatoms were collected from three streams that drain the Great Marsh at Indiana Dunes National Lakeshore. Diatom communities, water chemistry, and land use were measured at each site to test the hypothesis that differences in land use indirectly affect diatom communities, through changes in water quality. Relationships among these variables were examined by correlation, cluster, and detrended correspondence analysis. Several water chemistry variables were correlated to several land-use categories. Diatom species diversity was most variable in disturbed areas with poorer water quality and was correlated with land use and total alkalinity, total hardness, and specific conductance. Sites within each stream were grouped in terms of their diatom assemblage by both cluster and detrended correspondence analysis with but two exceptions in Dunes Creek. Diatom communities in the three streams responded to land use through its effects on water quality. The results of this study demonstrate the use of diatom assemblages as indicators of water quality, which can be linked to land use in a watershed.

Indiana