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USGS1963

Water resources of Red River Parish, Louisiana

Red River Parish is on the eastern flank of the Sabine uplift in northwestern Louisiana. The 'area is underlain by lignitic clay and sand of Paleocene and Eocene age which dip to the east at the rate of about 30 feet per mile. The Red River is entrenched in these rocks in the western part of the parish. Alternating valley filling and erosion during the Quaternary period have resulted in the present lowland with flanking terraces. In the flood-plain area moderate to large quantities of very hard, iron-bearing water, suitable for irrigation, are available to wells in the alluvial sand and gravel of Quaternary age. The aquifer ranges in thickness from 20 to slightly more than 100 feet. It is recharged by downward seepage of rainfall through overlying clay and silt, by inflow from older sands adjacent to and beneath the entrenched valley, and by infiltration from the streams where the water table is below stream level during flood stages or as a result of pumping. Water levels are highest in the middle of the valley. Ground water moves mainly toward the Red River on the east and Bayou Pierre on the west, but small amounts move down the valley. Computations based on water-level and aquifer-test data indicate that the Quaternary alluvium contains more than 330 billion gallons of ground water in storage and that the maximum discharge of ground water to the streams is slightly more than 30 mgd (million gallons per day). At times of high river stage, surface water flows into the aquifer at a rate that depends in part upon the height and duration of the river stage. Moderate supplies of soft, iron-bearing water may be obtained from dissected Pleistocene terrace deposits that flank the flood plains of the Red River and Black Lake Bayou. However, the quantity of water that can be pumped from these deposits varies widely from place to place because of differences in the areal extent and saturated thickness of the segments of the deposits; this extent and thickness are governed in turn by the amount of erosion the deposits have undergone. Beds of fine-grained lignitic sands of Tertiary age contain water of generally good quality to depths of 150 to 450 feet. The thinness and low permeability of the sands restrict their development to low-yield wells. Water from these sands in the western part of the parish, where they lie beneath the alluvial valley, is more mineralized than that from the younger Tertiary sands exposed in the east-central area. Streamflow records have been collected on the principal streams in Red River Parish since 1939. Additional spot low-flow data were obtained on several small streams originating within the parish for a study made in connection with the preparation of this report. Quality-of-water data for streams in the parish were collected on an occasional spot-sampling basis prior to and during this investigation. The largest source of surface water in the parish is the Red River, which drains approximately 63,400 square miles upstream from the parish. The Red River has an average flow of about 13,100 cfs (cubic feet per second), or about 8,500 mgd. Many of the streams that drain the upland area are not dependable sources of supply because their flows are not well sustained during dry seasons. The average annual precipitation over the parish is about 52 inches, of which about 17 inches becomes runoff; this runoff is equivalent to a continuous flow of about 1.25 cfs per square mile. Seasonal and annual runoff varies, but no significant trends have been noticed. The principal surface-water problems in the parish pertain to flood control, drainage, irrigation, and navigation. Flood problems have been alleviated considerably by the operation of Denison Dam (Lake Texoma), the completion of levees on the Red River, channel improvements on Bayou Pierre, and the completion of Wallace Lake reservoir on Cypress Bayou. There are wet lands along the Red River that would be very productive if properly drained

Water Supply Paper↗

USGS2018

Role of fault gouge during Interaction between hydraulic fracture and a preexisting fracture

Enhanced reservoir connectivity generally requires maximizing the intersection between hydraulic fracture (HF) and preexisting underground natural fractures (NF), while having the hydraulic fracture continue to propagate across the natural fractures. Observations of downhole core samples suggest that these natural fractures are in fact veins filled with minerals such as calcite (Mighani et al., 2016). We study this interaction during the approach of a hydraulic fracture to a smooth saw-cut fracture under triaxial stress conditions. The specimen is Solnhofen limestone, a fine-grained (<5 µm grain), low permeability (<10 nD) carbonate. The differential stress (1-20 MPa) and inclination of the fault which determines the approach angle, θ (30, 60°) are the experimental variables. We conduct the experiments on both bare surface and gouge-filled fault surfaces. The gouge is a 1 mm thick crushed powder of Solnhofen limestone with <106 µm grain size. During the hydraulic fracture, acoustic emissions (AE), inferred slip velocity, axial stress and pore pressure are recorded at a 5 MHz sampling rate. The hydraulic fracture was able to cross the bare surface fault with small induced fault slip. The fault gouge increased the coefficient of friction significantly from 0.12 (bare, polished surface) to > 0.44 (gouged layer). However, the gouge-filled fault arrested the hydraulic fracture and generated a slip event with different characteristics: 1- The stress drop was larger while the generated AE signals had lower magnitude. 2- Slip velocity recorded by the vibrometer was of the same order of magnitude for the bare and gouge-filled faults, but the slip duration increased from 29 µsec for bare surface to ~2.5 msec (~90 times longer rise time) for the gouge-filled fault. The experiments suggest that the gouge-filled fault can accommodate much larger displacement while promoting slow slip on the fault which is harder to detect as AE signals. The observed long duration slip events are similar to the field observations of the long period and long duration (LPLD) events during the stimulation of clay-rich shale formations (Zoback et al., 2012). While the intrinsic low strength, high ductility, and unfavorably oriented natural fractures in shale formations are expected to reduce the occurrence of induced seismicity, our experiments suggest an additional mechanism for the observed LPLD events, i.e. the role of fault gouge. They also suggest that the microseismic detection techniques may under-predict the stimulated volume as the activation of natural gouge-filled fractures may proceed aseismically.

Conference Paper↗

USGS2019

Water-quality and geochemical variability in the Little Arkansas River and Equus aquifer, south-central Kansas, 2001–16

The city of Wichita’s water supply currently (2019) comes from two primary sources: Cheney Reservoir and the Equus Beds aquifer. The Equus Beds aquifer storage and recovery project was developed to help the city of Wichita meet increasing future water demands. Source water for artificial recharge comes from the Little Arkansas River during above-base-flow conditions, is treated using National Primary Drinking Water Regulations as a guideline, and is injected into the Equus Beds aquifer through recharge wells or surface spreading basins for later use. The Equus Beds aquifer storage and recovery project currently (2019) consists of two coexisting phases. Phase I began in 2007 and captures Little Arkansas River water and indirect streambank diversion well water for aquifer recharge using 4 wells and 2 recharge basins. Phase II began in 2013 and currently (2019) includes a surface-water treatment facility, a river intake facility, eight recharge injection wells, and a third recharge basin. The U.S. Geological Survey, in cooperation with the City of Wichita, completed this study to summarize water-quality and geochemical variability of the Equus Beds aquifer. Data in this report can be used to establish baseline conditions before implementing artificial aquifer recharge further, document groundwater quality, evaluate changing conditions, identify environmental factors affecting groundwater, provide science-based information for decision making, and help meet regulatory monitoring requirements. Physicochemical properties were measured and water-quality data were collected from 2 Little Arkansas River surface-water sites and 63 Equus Beds aquifer groundwater sites, including 38 areal assessment index wells (IWs) during 2001 through 2016. Data collection included discrete samples and additional continuous measurements at selected sites. Discretely collected samples were analyzed for physicochemical properties, dissolved solids, primary ions, nutrients (nitrogen and phosphorus species), organic carbon, indicator bacteria, trace elements, arsenic species, organic compounds, and radioactivity. This report focuses discussion on aquifer water quality. Federal drinking-water criteria were used to evaluate aquifer water quality. Primary drinking-water criteria are those that are enforceable for public drinking water. Secondary criteria are those that can cause aesthetics or tastes that are unpleasant. Continuously collected data at a subset of sites included streamflow, groundwater levels, water temperature, specific conductance, pH, oxidation-reduction potential (ORP), dissolved oxygen, turbidity, nitrate plus nitrite, and fluorescent dissolved organic matter. Continuous measurement of physicochemical properties in near-real time allowed characterization of Little Arkansas River surface water and Equus Beds aquifer groundwater during conditions and time scales that would not have been possible otherwise and served as a complement to discrete water-quality sampling. During 2001 through 2016, less than 1 percent of chloride and nitrate plus nitrite, 7 percent of dissolved iron, 48 percent of dissolved manganese, 12 percent of dissolved arsenic, and 39 percent of atrazine detections in surface-water samples exceeded their respective Federal primary or secondary drinking-water criteria. None of the surface-water samples collected exceeded the Federal sulfate criterion, and every sample had detections of total coliform bacteria during the study. Constituents of concern in the Equus Beds aquifer exceeded their respective Federal criteria throughout the study period and included chloride, sulfate, nitrate plus nitrite, Escherichia coli ( E. coli ), total coliforms, and dissolved iron and arsenic species. About 5 percent of shallow (less than 80 feet) and 7 percent of deep (greater than 80 feet) IW chloride sample concentrations exceeded the secondary Federal criterion of 250 milligrams per liter (mg/L). Chloride tended to exceed its criterion in shallow and deep wells along the Arkansas River and near Burrton, Kansas, an area with past oil and gas activities. Chloride concentrations near Burrton were larger in the deep parts of the aquifer. About 18 percent of shallow and 13 percent of deep IW sulfate sample concentrations exceeded the secondary Federal criterion of 250 mg/L. Mean sulfate concentrations tended to exceed the criterion in the central part of the study area. Shallow IW mean nitrate plus nitrite (hereafter referred to as “nitrate”) was substantially larger than mean deep IW nitrate. Geochemical conditions in the deeper aquifer reduced forms of nitrogen to species such as ammonia. About 15 percent of shallow and less than 1 percent of deep IW nitrate sample concentrations exceeded the Federal criterion of 10 mg/L. Mean shallow IW nitrate concentrations exceeded the criterion in the northeastern and southeastern parts of the study area; on average, deep IW nitrate concentrations did not exceed the criterion. E. coli and fecal coliform bacteria detections were usually at or near the detection limit. E. coli was detected in 3 percent of shallow and deep IWs, and fecal coliform bacteria were detected in 8 percent of shallow and 6 percent of deep IWs. Total coliforms were detected in 24 percent of shallow and 12 percent of deep IWs. E. coli coliphage was detected in two shallow IW samples (1 percent of samples) at the detection limit and was not detected in deep IW samples. Dissolved iron was detected in 51 percent of shallow and 62 percent of deep IW samples. Dissolved iron concentrations exceeded the secondary Federal criterion of 0.3 mg/L in 38 percent of shallow and 46 percent of deep IW samples. Mean dissolved iron concentrations were largest mostly in the central and northwest part of the study area corresponding to an area of the aquifer where aquifer material is more clay-rich. The distribution of large dissolved iron concentrations was similar to that of large sulfate concentrations. About 55 percent of shallow and 92 percent of deep IW dissolved manganese samples exceeded the secondary Federal criterion of 0.05 mg/L. Almost all samples from the central and northern parts of the study area had mean dissolved manganese concentrations that exceeded the Federal criterion in the shallow part of the aquifer. Mean dissolved manganese concentrations in the shallow part of the aquifer were substantially large (greater than 1,000 micrograms per liter [μg/L]) in wells near the Little Arkansas River and in the central part of the study area because of chemically reducing conditions in the aquifer that likely related to larger percentages of clay in the aquifer material. Concentrations of dissolved arsenic species generally were larger in the deep parts of the aquifer. Arsenite was the dominant form of arsenic on average in shallow (52 percent) and deep (55 percent) IWs. About 12 percent of shallow and 34 percent of deep IW dissolved arsenic sample concentrations exceeded the Federal primary drinking criterion of 10 μg/L. Shallow IW dissolved arsenic concentrations were larger near the Little Arkansas River and the center of the study area; large shallow IW dissolved arsenic concentrations (10–50 μg/L) in the center of the study area correspond to areas that have had the most water-level recovery since the historical low in 1993. Mean ORP in shallow IWs generally decreased with increasing water-level depths and were inversely related to mean dissolved arsenic concentrations because of more reducing conditions (smaller ORP) at larger depths below the land surface. Larger dissolved arsenic concentrations in the shallow parts of the aquifer were associated with decreases in water levels and a subsequent decrease in ORP and thus more reducing conditions. Atrazine was detected in about 58 percent of shallow and 28 percent of deep IWs and did not exceed the primary Federal criterion of 3 μg/L in any groundwater samples. Atrazine concentrations in shallow IWs generally were largest in the northwest part of the study area near the North Branch Kisiwa Creek, and atrazine concentrations in deep IWs generally were largest most often in the southern part of the study area. Gross α radioactivity concentrations exceeded the primary Federal criterion of 15 picocuries per liter in 4 percent of shallow IW samples. Gross α and gross β radioactivity concentrations generally were larger in the southern third of the aquifer. Most groundwater-sample-simulated minerals saturation indices (SIs) were consistently negative (undersaturated). Minerals that had SI values that were consistently or typically positive (oversaturated) included iron oxide, hydroxide, and quartz-group minerals. Several SI values for arsenic- and manganese-bearing minerals were consistently negative. Some manganese-bearing mineral SI values ranged from undersaturated to oversaturated in shallow and deep IWs during the study. Several carbonate minerals in shallow and deep IWs varied across their equilibrium state. Calcite SI values were larger more often in the deep parts of the aquifer and did not show a clear distributional pattern. Mean and median calcite SI values for shallow and deep IWs were negative (undersaturated) indicating the potential for calcite dissolution if calcite is present for a substantial part of the study period. However, some individual calcite SI values in this study indicated saturation and subsequent calcite precipitation may occur in the study area, potentially resulting in formation of calcite mineral deposits that may reduce efficiency of injection wells. SI values with respect to iron hydroxide varied across their equilibrium states. Mean and median SI values with respect to iron hydroxide were undersaturated in shallow and deep IWs; however, some samples had positive SI values indicating there is potential for iron hydroxide precipitation, possibly caused by leaching and oxidation of iron-containing minerals, like pyrite, in the aquifer material.

Kansas↗

USGS1981

E-field ratio telluric survey near the Big Maria Mountains, Riverside County, California

The U.S. Geological Survey (USGS) under the Wilderness Act (Public Law 88-577) and the Federal Land Policy and Management Act (Public Law 94-579) has the responsibility, along with the U.S. Bureau of Mines, to survey certain areas in order to determine their mineral resource potential. This report presents results of three electric-field ratio telluric traverses conducted as part of the Bureau of Land Management Wilderness Program in the Big Maria Mountains, Riverside County, Calif. The telluric traverses were run on the southwest side of the Big Maria Mountains in an attempt to define the location of major buried faults near the eroded front of the range. E-field ratio tellurics is a descriptive name applied to the electrical exploration technique used in this survey. The telluric method refers to the measurement of the earth's electric field generated by induction from natural electromagnetic waves arriving at the surface. The E-field ratio telluric method uses a receiving array of three electrodes spaced equidistant and inline. This array is, in effect, two colinear dipoles sharing a common electrode. The potential difference across each dipole is then proportional to the component of the telluric field in the direction of the array. This configuration permits the measurement of the ratio of the telluric field at each dipole in the direction of the dipole line, and hence the name. The traverse data is extended by moving the three-electrode array forward one dipole length so that the forward electrode becomes the center electrode for the next ratio measurement. Electric-field data so obtained are proportional to the square root of the apparent resistivity of the earth at the location of the dipoles. However, because the apparent resistivity can be a function of the dipole direction, it is important to know the orientation of the dipoles with respect to major structures. Because the resistivity of fluid-saturated earth materials is largely dependent on the porosity of the rocks, the salinity of the pore fluid, and the presence of clays or similar material where surface conduction is high, alluvial fill, argillite and similar rocks tend to have low resistivities whereas igneous or high-grade metamorphic rocks have high resistivities. Variation in the electrical properties along a traverse may then be used to infer lithologic or structural changes.

California↗

USGS2003

Geologic map of the Rio Puerco quadrangle, Bernalillo and Valencia Counties, New Mexico

The Rio Puerco quadrangle is located southwest of Albuquerque in central New Mexico and covers part of the western part of the Isleta Reservation. The U.S. Geological Survey, the New Mexico Bureau of Geology and Mineral Resources, and the University of New Mexico have conducted geologic mapping on the Isleta Reservation and vicinity as part of the Middle Rio Grande Basin Project. The map area contains surficial deposits, calcic soils, fluvial deposits of the Rio Puerco, deposits of the Santa Fe Group, and three volcanic fields. The area is characterized by predominantly north-trending normal faults with generally down-to-the-east movement. Post-Santa Fe Group deposits are composed of surficial deposits (Pleistocene-Holocene) and fluvial deposits of the Rio Puerco (Pleistocene-Holocene). The surficial deposits are divided into eolian, alluvial, colluvial, and landslide deposits. The fluvial deposits of the Rio Puerco consist of four terrace and present channel deposits. The Santa Fe Group is divided into lower and upper parts. The lower part of the Santa Fe Group is exposed near the southwestern corner of the study area where deposits consist of reddish-brown mudstone and sandstone correlated to the Popotosa Formation (Unit 1) of Lozinsky and Tedford (1991). They interpreted deposition of the unit in a basin-floor playa setting. The Popotosa Formation is in fault contact to the east with deposits of the upper Santa Fe Group. The upper Santa Fe Group is derived from major tributary fluvial systems (ancestral Rio Puerco Puerco and possibly the Rio San Jose drainages) draining the adjacent Colorado Plateau and Sierra Nacimiento and correlated to parts of Kelley's (1977) Ceja Formation of the Santa Fe Group and equivalent to Machette's (1978) Sierra Ladrones Formation, Connell's Arroyo Ojito Formation (Connell and others, 1999, and Maldonado's lithofacies of the Isleta Reservation (Maldonado and Atencio,1998a, b). The group also locally includes a fine- grained unit (lower Pleistocene) referred to here as the sand, silt, and clay of Chavez Grant (Qsc). The Ceja Formation of the Santa Fe Group as defined here is divided into the following units in descending stratigraphic order: (1) upper sand and gravel unit (upper Pliocene), (2) middle silt, sand, and clay unit (upper Pliocene), and (3) lower sand and gravel unit (Pliocene). The three volcanic fields in the map area are: (1) basalt of Cat Hills, dated at 98-110 ka and composed of seven lava flows and four cinder cones; the flows overlie calcic soils that overlie the upper sand and gravel unit of the Ceja Formation; (2) lava flow of Cat Mesa, dated at about 3 Ma and interfingers with the upper part of the Ceja Formation; (3) diabase of Mohinas Mountain, dated at 8.3 Ma (Baldridge and others, 1987) and intrudes the Popotosa Formation. Numerous high-angle faults cut the area but are mostly buried. The faults generally trend north but deviate to the northwest and northeast. The major normal faults are the Cat Mesa and Mohinas Mountain faults.

Miscellaneous Field Studies Map↗

USGS1996

Water quality of surficial aquifers in the Georgia-Florida Coastal Plain

The National Water Quality Assessment Program of the U.S. Geological Survey established the Georgia-Florida Coastal Plain study unit in 1991. The ground-water study-unit survey was conducted in 1993 to provide a broad overview of water quality in surficial aquifers. Three land resource provinces were included in the Georgia-Florida Coastal Plain study-unit survey: the Central Florida Ridge, the Coastal Flatwoods, and the Southern Coastal Plain. The U.S. Geological Survey sampled 37 wells in surficial aquifers, 18 in the Coastal Flatwoods and 19 in the Southern Coastal Plain. The Florida Department of Environmental Protection sampled 27 wells tapping surficial aquifers in the Central Florida Ridge as part of the background ground-water quality monitoring network from 1985 through 1989. The data were used to characterize water quality in surficial aquifers of the Central Florida Ridge. Results of the study-unit survey indicated that dissolved solids concentrations in ground water were mostly less than 100 mg/L (milligrams per liter). Higher medians of pH, specific conductance, and concentrations of calcium, bicarbonate, and dissolved solids were measured in samples from the Central Florida Ridge compared to the Southern Coastal Plain and Coastal Flatwoods, probably because of a greater percentage of carbonate minerals in aquifer materials. The U.S. Environmental Protection Agency secondary maximum contaminant level for iron of 300 ug/L (micrograms per liter) in drinking water was exceeded in 15 of 45 samples. Concentrations of nitrate as nitrogen were less than 3.0 mg/L in most samples (74 percent), indicating little or no influence from human activity. Only five samples (9 percent) had concentrations above 10 mg/L, the U.S. Environmental Protection Agency maximum contaminant level for nitrate concentration in drinking water. Significantly lower median concentrations of nitrate were measured in samples from polyvinyl chloride monitoring wells with diameters less than 6 inches than in large diameter, uncased, or iron-cased wells. The median nitrate concentration was 0.05 mg/L in water from monitoring wells, 1.0 mg/L in samples from iron cased wells, and 2.0 mg/L in samples from uncased wells. Concentrations of volatile organic compounds were mostly less than the detection levels and exceeded 1 ug/L in only four samples. Compounds detected at concentrations greater than 1 ug/L were: tetrachloroethane (8.77 ug/L), toluene (23 ug/L) and chloromethane (21 ug/L). Atrazine, desethyl-atrazine, and metolachlor were the only pesticides detected; concentrations were less than 0.02 ug/L, except for metolachlor (2.5 ug/L). Detection of organic compounds in surficial aquifers may be associated with specific activities or sources near the well. Concentrations of radon exceeded the U.S. Environmental Protection Agency proposed maximum contaminant level of 300 picocuries per liter (pCi/L) in 33 samples from wells on the Coastal Flatwoods and the Southern Coastal Plain. Concentrations as high as 13,000 pCi/L were detected in northern Florida. Although uranium concentrations were less than 1 ug/L in all but one sample (1.3 ug/L) from the Southern Coastal Plain, elevated radon concentrations indicate that uranium is present in aquifer material. Uranium is most likely sorbed to iron oxides and clays in subsurface materials. Tritium concentrations indicated that ground water was recharged by precipitation during the past 40 years. Higher concentrations of tritium in ground water were found in the northern part of the study area and may be related to Savannah River Nuclear Facility.

Florida, Georgia↗

USGS2014

Aquifers of Arkansas: protection, management, and hydrologic and geochemical characteristics of groundwater resources in Arkansas

Sixteen aquifers in Arkansas that currently serve or have served as sources of water supply are described with respect to existing groundwater protection and management programs, geology, hydrologic characteristics, water use, water levels, deductive analysis, projections of hydrologic conditions, and water quality. State and Federal protection and management programs are described according to regulatory oversight, management strategies, and ambient groundwater-monitoring programs that currently (2013) are in place for assessing and protecting groundwater resources throughout the State. Physical attributes, groundwater geochemistry, and groundwater quality are described for each of the 16 aquifers of the State. Information in regard to the hydrology and geochemistry of each of the aquifers is summarized from about 550 historical and recent publications. Additionally, more than 8,000 sites with groundwater-quality data were obtained from the U.S. Geological Survey National Water Information System and the Arkansas Department of Environmental Quality databases and entered into a spatial database to investigate distribution and trends in chemical constituents for each of the aquifers. The 16 aquifers of the State were divided into two major physiographic regions of the State: the Coastal Plain Province (referred to as Coastal Plain) of eastern and southern Arkansas, which includes 11 of the 16 aquifers, and the Interior Highlands Division (referred to as Interior Highlands) of western Arkansas, which includes the remaining 5 aquifers. The 11 aquifers in the Coastal Plain consist of various geologic units that are Cenozoic in age and consist primarily of Cretaceous, Tertiary, and Quaternary sands, gravels, silts, and clays. Groundwater in the Coastal Plain represents one of the most valuable natural resources in the State, driving the economic engines of agriculture, while also supplying abundant water for commercial, industrial, and public-supply use. In terms of age from youngest to oldest, the aquifers of the Coastal Plain include Quaternary alluvial aquifers, including the Mississippi River Valley alluvial aquifer (the most important aquifer in Arkansas in terms of volume of use and economic benefits), the Jackson Group (a regional confining unit that served for decades as an important source of domestic supply), and the Cockfield, Sparta, Cane River, Carrizo, Wilcox, Nacatoch, Ozan, Tokio, and Trinity aquifers. The Mississippi River Valley alluvial aquifer accounts for approximately 94 percent of all groundwater used in the State, and the aquifer is used primarily for irrigation purposes. The Sparta aquifer is the second most important aquifer in terms of use, and the aquifer was used in the past dominantly as a source of public and industrial supply, although increasing irrigation use is occurring because of critically declining water levels in the Mississippi River Valley alluvial aquifer. Other aquifers of the Coastal Plain generally are used as important local sources of domestic, industrial, and public supply, in addition to other minor uses. Water quality generally is good for all aquifers of the Coastal Plain, except for elevated iron concentrations and localized areas of high salinity. The high salinity results from intrusion from underlying formations, evapotranspiration processes in areas of low recharge, and inadequate flushing in downgradient areas of residual salinity from deposition in marine environments. Trends in the spatial distribution of individual chemical constituents are related to position along the flow path for most aquifers of the Coastal Plain. These trends include elevated iron and nitrate concentrations with lower pH values and dissolved solids in groundwater from the outcrop areas, transitioning to lower iron and nitrate (related to changes in redox) and higher pH and dissolved solids (dominantly from the dissolution of carbonate minerals) in groundwater downgradient from outcrop areas. Groundwater generally trended from a calcium- to a sodium-bicarbonate water type with increasing cation exchange along the flow path. The Interior Highlands of western Arkansas has less reported groundwater use than other areas of the State, reflecting a combination of factors. These factors include prevalent and increasing use of surface water, less intensive agricultural uses, lower population and industry densities, lesser potential yield of the resource, and lack of detailed reporting. The overall low yields of aquifers of the Interior Highlands result in domestic supply as the dominant use, with minor industrial, public, and commercial-supply use. Where greater volumes are required for growth of population and industry, surface water is the greatest supplier of water needs in the Interior Highlands. The various aquifers of the Interior Highlands generally occur in shallow, fractured, well-indurated, structurally modified bedrock of this mountainous region of the State, as compared to the relatively flat-lying, unconsolidated sediments of the Coastal Plain. In terms of age from youngest to oldest, the aquifers of the Interior Highlands include: the Arkansas River Valley alluvial aquifer, the Ouachita Mountains aquifer, the Western Interior Plains confining system, the Springfield Plateau aquifer, and the Ozark aquifer. Spatial trends in groundwater geochemistry in the Interior Highlands differ greatly from trends noted for aquifers of the Coastal Plain. In the Coastal Plain, the prevalence of long regional flow paths results in regionally predictable and mappable geochemical changes along the flow paths. In the Interior Highlands, short, topographically controlled flow paths (from hilltops to valleys) within small watersheds represent the predominant groundwater-flow system. As such, dense data coverage from numerous wells would be required to effectively characterize these groundwater basins and define small-scale geochemical changes along any given flow path for aquifers of the Interior Highlands. Changes in geochemistry generally were related to rock type and residence time along individual flow paths. Dominant changes in geochemistry for the Ouachita Mountains aquifer and the Western Interior Plains confining system are attributed to rock/water interaction and changes in redox zonation along the flow path. In these areas, groundwater evolves along flow paths from a calcium- to a sodium-bicarbonate water type with increasing reducing conditions resulting in denitrification, elevated iron and manganese concentrations, and production of methane in the more geochemically evolved and strongest reducing conditions. In the Ozark and Springfield Plateau aquifers, rapid influx of surface-derived contaminants, especially nitrogen, coupled with few to no attenuation processes was attributed to the karst landscape developed on Mississippian- and Ordovician-age carbonate rocks of the Ozark Plateaus. Increasing nitrate concentrations are related to increasing agricultural land use, and areas of mature karst development result in higher nitrate concentrations than areas with less karst features.

Arkasas↗

USGS1996

Summary of the Snake River plain Regional Aquifer-System Analysis in Idaho and eastern Oregon

Regional aquifers underlying the 15,600-square-mile Snake River Plain in southern Idaho and eastern Oregon was studied as part of the U.S. Geological Survey's Regional Aquifer-System Analysis program. The largest and most productive aquifers in the Snake River Plain are composed of Quaternary basalt of the Snake River Group, which underlies most of the 10,8000-square-mile eastern plain. Aquifer tests and simulation indicate that transmissivity of the upper 200 feet of the basalt aquifer in the eastern plain commonly ranges from about 100,000 to 1,000,000 feet squared per day. However, transmissivity of the total aquifer thickness may be as much as 10 million feet squared per day. Specific yield of the upper 200 feet of the aquifer ranges from about 0.01 to 0.20. Average horizontal hydraulic conductivity of the upper 200 feet of the basalt aquifer ranges from less than 100 to 9,000 feet per day. Values may be one to several orders of magnitude higher in parts in individual flows, such as flow tops. Vertical hydraulic conductivity is probably several orders of magnitude lower than horizontal hydraulic conductivity and is generally related to the number of joints. Pillow lava in ancestral Snake River channels has the highest hydraulic conductivity of all rock types. Hydraulic conductivity of the basalt decreases with depth because of secondary filling of voids with calcite and silica. An estimated 80 to 120 million acre-feet of water is believed to be stored in the upper 200 feet of the basalt aquifer in the eastern plain. The most productive aquifers in the 4,800-square-mile western plain are alluvial sand and gravel in the Boise River valley. Although aquifer tests indicate that transmissivity of alluvium in the Boise River valley ranges from 5,000 to 160,000 feet squared per day, simulation suggests that average transmissivity of the upper 500 feet is generally less than 20,000 feet squared per day. Vertically averaged horizontal hydraulic conductivity of the upper 500 feet of alluvium ranges from about 4 to 40 feet per day; higher values can be expected in individual sand and gravel zones. Vertical hydraulic conductivity is considerably lower because of the presence of clay layers. Hydraulic heads measured in piezometers, interpreted from diagrams showing ground-water flow and equipotential lines and estimated by computer simulation, demonstrate that water movement is three dimensional through the rock framework. Natural recharge takes place along the margins of the plain where head decreases with depth; discharge takes place near some reaches of the Snake River and the Boise River where head increases with depth. Geothermal water in rhyolitic rocks in the western plain and western part of the eastern plain has higher hydraulic head than the overlying cold water. Geothermal water, therefore, moves upward and merges into the cold-water system. Basin water-budget analyses indicate that the volume of cold water. Carbon-14 age determinations, which indicate that residence time of geothermal water is 17,700 to 20,300 years, plus or minus 4,000 years, imply slow movement of water through the geothermal system. Along much of its length, the Snake River gains large quantities of ground water. On the eastern plain, the river gained about 1.9 million acre-feet of water between Blackfoot and Neeley, Idaho, in 1980. Between Milner and King Hill, Idaho, the river gained 4.7 million acre-feet, mostly as spring flow from the north side. Upstream from Blackfoot and in the vicinity of Lake Walcott, the rover loses flow to ground water during parts or all of the year. On the western plain, river gains from ground water are small relative to those on the eastern plain; most are from seepage. Streams in tributary drainage basins supply calcium/bicarbonate type and calcium/magnesium/bicarbonate type water to the plain. Water type is a reflection of the chemical composition of rocks in the drainage basin, Concentrations of dissolved solids are smallest, about 50 milligrams per liter, in streams such as the Boise River that drain areas of granitic rocks; concentrations are greatest, about 400 milligrams per liter, in streams such as the Owyhee and Raft Rivers that drain area of sedimentary rocks. Water chemistry reflects the interaction of surface water and ground water. The chemical composition of ground water in the plain is essentially the same as that in streamflow and groundwater discharge from tributary drainage basins. Tributary drainage basins supplied 85 percent of the ground-water recharge in the eastern plain during 1980 and a nearly equivalent percentage of the solute load in ground water; human activities and dissolution of minerals supplied the other solutes. Dissolved-solids concentrations in ground water were generally less than 400 milligrams per liter. Water from the lower geothermal system is chemically different from water from the upper cold-water system. Geothermal water typically has greater concentrations of sodium, bicarbonate, sulfate, chloride, fluoride, silica, arsenic, boron, and lithium and smaller concentrations of calcium, magnesium, and hydrogen. Difference are attributed to ion exchange as geothermal moves through the rock framework. Irrigation, mostly on the Snake River Plain, accounted for about 96 percent of consumptive water use in Idaho during 1980. The use of surface water for irrigation for more than 100 years has caused major changes in the hydrologic system on the plain. Construction of dams, reservoirs, and diversifications effected planned changes in the surface-water system but resulted in largely unplanned changes in the ground-water system. During those years of irrigation, annual recharge in the main part of the eastern plain increased to about 6.7 million acre-feet in 1980, or by about 70 percent. Most of the increase was from percolation of surface water diverted for irrigation. From preirrigation to 1952, groundwater storage increased about 24 million acre-feet, and storage decreased from 1952 to 1964 and from 1976 to 1980 because of below-normal precipitation and increased withdrawals of ground water for irrigation. Annual ground-water discharge increased to about 7.1 million acre-feet in 1980, or about 80 percent since the start of irrigation. About 10 percent of the 1980 total discharge was ground-water pumpage. About 3.1 million acres, or almost one-third of the plain, was irrigated during 1980: 2.0 million acres with surface water, 1.0 million acres with ground water, and 0.1 million acres with combined surface and ground water. About 8.9 million acre-feet of Snake River water was diverted for irrigation during 1980 and 2.3 million acre-feet of ground water was pumped from 5,300 wells. Most irrigation wells on the eastern plain are open to basalt. About two-thirds of them yield more than 1,500 gallons per minute with a reported maximum of 7,240 gallons per minute; drawdown is less than 20 feet in two-thirds of the wells. Most irrigation wells on the western plain are open to sedimentary rocks. About one-third of them yield more than 1,00 gallons per minute with a reported maximum of 3,850 gallons per minute; drawndown is less than 20 feet in about one-fifth of the wells. The major instream use of water on the Snake River Plain is hydroelectric power generation. Fifty-two million acre-feet of water generated 2.6 million megawatthours of electricity during 1980. Digital computer ground-water flows models of the eastern and western plain reasonably simulated regional changes in water levels and ground-water discharges from 1880 (preirrigation) to 1980. Model results support the concept of three-dimensional flow and the hypotheses of no underflow between the eastern and western plain. Simulation of the regional aquifer system in the eastern plain indicates that is 1980 hydrologic conditions, including pumpage, were to remain the same for another 30 years, moderate declines in ground-water levels and decreases in spring discharges would continue. Increased ground-water pumpage to irrigate an additional 1 million acres could cause ground-water levels to decline a few tens of feet in the central part of the plain and could cause corresponding decreases in ground-water discharge. A combination of actions such as increased ground-water pumpage and decreased use of surface water for irrigation (resulting in reduced recharge) would accentuate the changes.

Idaho;Oregon↗

USGS2006

Regional evaluation of the hydrogeologic framework, hydraulic properties, and chemical characteristics of the intermediate aquifer system underlying southern west-central Florida

Three major aquifer systems-the surficial aquifer system, the intermediate aquifer system, and the Floridan aquifer system-are recognized in the approximately 5,100-square-mile southern west-central Florida study area. The principal source of freshwater for all uses is ground water supplied from the three aquifer systems. Ground water from the intermediate aquifer system is considered only moderately abundant compared to the Upper Floridan aquifer, but it is an important source of water where the Upper Floridan aquifer contains water too mineralized for most uses. In the study area, the potential ground-water resources of the intermediate aquifer system were evaluated by regionally assessing the vertical and lateral distribution of hydrogeologic, hydraulic, and chemical characteristics. Although the intermediate aquifer system is considered a single entity, it is composed of multiple water-bearing zones separated by confining units. Deposition of a complex assemblage of carbonate and siliciclastic sediments during the late Oligocene to early Pliocene time resulted in discontinuities that are reflected in transitional and abrupt contacts between facies. Discontinuous facies produce water-bearing zones that may be locally well-connected or culminate abruptly. Changes in the depositional environment created the multilayered intermediate aquifer system that contains as many as three zones of enhanced water-bearing capacity. The water-bearing zones consist of indurated limestone and dolostone and in some places unindurated sand, gravel, and shell beds, and these zones are designated, in descending order, as Zone 1, Zone 2, and Zone 3. Zone 1 is thinnest (<80 feet thick) and is limited to <20 percent (southern part) of the study area. Zone 2, the only regionally extensive zone, is characterized by moderately low permeability. Zone 3 is found in about 50 percent of the study area, has the highest transmissivities, and generally is in good hydraulic connection with the underlying Upper Floridan aquifer. In parts of the study area, particularly in southwestern Hillsborough County and southeastern De Soto and Charlotte Counties, Zone 3 likely is contiguous with and part of the Upper Floridan aquifer. Transmissivity of the intermediate aquifer system ranges over five orders of magnitude from about 1 to more than 40,000 feet squared per day (ft2/d), but rarely exceeds 10,000 ft2/d. The overall transmissivity of the intermediate aquifer system is substantially lower (2 to 3 orders of magnitude) than the underlying Upper Floridan aquifer. Transmissivity varies vertically among the zones within the intermediate aquifer system; Zone 2 has the lowest median transmissivity (700 ft2/d), Zone 1 has a moderate median transmissivity (2,250 ft2/d), and Zone 3 has the highest median transmissivity (3,400 ft2/d). Additionally, the transmissivity varies geographically (from site to site) within a zone. Specifically, a region of relatively low transmissivity (<100 ft2/d) throughout the vertical extent of the intermediate aquifer system is present in the central part of the study area. This low transmissivity region is encompassed by a larger region of moderately low transmissivity (<1,000 ft2/d) that covers a large part of the study area. Clay beds and fine-grained carbonates form the confining units between the water-bearing zones and are characterized by low leakance. Leakance through the intermediate aquifer system confining units ranges over 4 orders of magnitude from 4.2x10-7 to 6.0x10-3 feet per day per foot [(ft/d)/ft]. Despite the large range, the geometric mean and median leakances of individual confining units are within the same order of magnitude, 10-5 (ft/d)/ft, which is 2 orders of magnitude less than the median leakance of the semiconfining unit within the Upper Floridan aquifer. Major ion concentrations in water from the intermediate aquifer system, and throughout the ground-water flow system, generally increase with depth. T

Scientific Investigations Report↗

USGS2025

Tracking diagenetic alteration of magnetic susceptibility in thrust ridge and slope basin sediments of the Cascadia margin (ODP Sites 1249 and 1252; IODP Site U1325)

We investigated sediment core records from the Cascadia Margin (Ocean Drilling Program Sites 1249 and 1252 at Hydrate Ridge; Integrated Ocean Drilling Program Site U1325 offshore Vancouver Island) using a Zr/Rb heavy mineral proxy from X-ray fluorescence (XRF) core scanning to identify intervals of primary detrital magnetic susceptibility (κ) and predict intervals where diagenesis caused magnetite dissolution by hydrogen sulfide. We also measured total sulfur (TS) content, grain size distributions, total organic carbon (TOC) content, and the magnetic mineral assemblage to further constrain the role of diagenesis on κ. Understanding how κ can be used to better characterize the varied effects of detrital and diagenetic signals in marine settings is important for understanding biogeochemical cycling and records of paleoenvironmental change. The upper 100 m of slope basin Site 1252 contains multiple intervals (> 90 m total) of decreased κ correlated with elevated TS content, consistent with dissolution of magnetite and precipitation of pyrite, iron monosulfides, and/or elemental sulfur. Similarly at the other slope basin site, Site U1325, κ is lower and TS is elevated in the interval between 24 and 51 mbsf, due to sulfide formation. At both slope basin sites, these low κ intervals correspond with high TOC, suggesting the possibility that organoclastic sulfate reduction (OSR) is likely a major driver of diagenetic alteration of κ at these sites. High TS:TOC ratios at Site U1325 suggests anaerobic oxidation of methane (AOM) during sulfate-methane transition zone (SMTZ) migration may have contributed to alteration of κ. In contrast, within the upper 90 m of Site 1249, a methane seep site at the summit of Hydrate Ridge, κ is almost entirely altered by diagenetic processes, with much of the low κ explained by a high degree of iron sulfide formation, while some intervals are affected by precipitation of magnetic iron sulfides that maintain or even increase κ. The presence of abundant methane seepage and gas hydrate as well as chemosynthetic seafloor fauna at this site, suggests that sulfide is released to the water column and AOM, rather than OSR, drives diagenetic alteration of κ at this site. Overall, the slope basin sites show episodic variation of κ that is influenced by TOC content, likely driven by changes in marine primary productivity and sedimentation rate, while the seep site shows consistently altered κ with lower TS content and no correlation with TOC. Methane seep environments likely experience loss of hydrogen sulfide to the water column and oxidation of hydrogen sulfide by seafloor seep fauna, which limits the amount of solid phase sulfur (pyrite, iron monosulfides, elemental sulfur) that can be precipitated within the sediments. In contrast, the migration of a buried SMTZ at slope basin sites results in enhanced sulfur precipitation within the sediments. This integrated magnetic and geochemical approach reveals the diagenetic production pathway and residence time of sulfide with the sediment column ultimately controls the style and degree of diagenetic loss of κ in marine sediments. This approach works best in environments with unaltered reference intervals/sites, consistent magnetic mineralogy, and clay-to-silt grain sizes.

Cascadia margin, Pacific Ocean↗

USGS2009

Evolution and preservation potential of fluvial and transgressive deposits on the Louisiana inner shelf: Understanding depositional processes to support coastal management

The barrier-island systems of the Mississippi River Delta plain are currently undergoing some of the highest rates of shoreline retreat in North America (~20 m/year). Effective management of this coastal area requires an understanding of the processes involved in shoreline erosion and measures that can be enacted to reduce loss. The dominant stratigraphy of the delta plain is fluvial mud (silts and clays), delivered in suspension via a series of shallow-water delta lobes that prograded across the shelf throughout the Holocene. Abandonment of a delta lobe through avulsion leads to rapid land subsidence through compaction within the muddy framework. As the deltaic headland subsides below sea level, the marine environment transgresses the bays and wetlands, reworking the available sands into transgressive barrier shorelines. This natural process is further complicated by numerous factors: (1) global sea-level rise; (2) reduced sediment load within the Mississippi River; (3) diversion of the sediment load away from the barrier shorelines to the deep shelf; (4) storm-induced erosion; and (5) human alteration of the littoral process through the construction of hardened shorelines, canals, and other activities. This suite of factors has led to the deterioration of the barrier-island systems that protect interior wetlands and human infrastructure from normal wave activity and periodic storm impact. Interior wetland loss results in an increased tidal prism and inlet cross-sectional areas, and expanding ebb-tidal deltas, which removes sand from the littoral processes through diversion and sequestration. Shoreface erosion of the deltaic headlands does not provide sufficient sand to balance the loss, resulting in thinning and dislocation of the islands. Abatement measures include replenishing lost sediment with similar material, excavated from discrete sandy deposits within the muddy delta plain. These sand bodies were deposited by the same cyclical processes that formed the barrier islands, and understanding these processes is necessary to characterize their location, extent, and resource potential. In this paper we demonstrate the dominant fluvial and marine-transgressive depositional processes that occur on the inner shelf, and identify the preservation and resource potential of fluvio-deltaic deposits for coastal management in Louisiana.

Geo-Marine Letters↗

USGS1959

Geology and ground-water resources of the upper Lodgepole Creek drainage basin, Wyoming, with a section on chemical quality of the water

The principal sources of ground-water supply in the upper Lodgepole Creek drainage basin-the part of the basin west of the Wyoming-Nebraska State line-are the Brule formation of Oligocene age, the Arikaree formation of Miocene age, the Ogallala formation of Pliocene age, and the unconsolidated deposits of Quaternary age. The Brule formation is a moderately hard siltstone that generally is not a good aquifer. However, where it is fractured or where the upper part consists of pebbles of reworked siltstone, it will yield large quantities of water to wells. Many wells in the Pine Bluffs lowland, at the east end of the area, derive water from the Brule. The Arikaree formation, which consists of loosely to moderately cemented fine sand, will yield small quantities of water to wells but is not thick enough or permeable enough to supply sufficient water for irrigation. Only a few wells derive water from it. The Ogallala formation consists of lenticular beds of clay, silt, sand, and gravel which, in part, are cemented with calcium carbonate. Only the lower part of the formation is saturated. Nearly all the wells in the upland part of the area tap the Ogallala, but they supply water in amounts sufficient for domestic and stock use only. Two of the wells have a moderately large discharge, and other wells of comparable discharge probably could be drilled in those parts of the upland where the saturated part of the Ogallala is fairly thick. Most of the unconsolidated deposits of Quaternary age are very permeable and, where a sufficient thickness is saturated, will yield large quantities of water to wells. These deposits are a significant source of water supply in the southeastern part of the area. The Chadron formation of Oligocene age, which underlies the Brule formation, is a medium- to coarse-grained sandstone where it crops out in the Islay lowland. No wells tap the Chadron, but it probably would yield small quantities of water to wells. It lies at a relatively shallow depth beneath most of the Islay lowland, near the west end of the area, and at a depth of about 800 feet beneath the Pine Bluffs lowland. In the latter area it probably is finer grained and may not be permeable enough to yield water to wells. All the ground water in the area is derived from precipitation. It is estimated that about 5 percent of the precipitation infiltrates directly to the zone of saturation. The remainder either is evaporated immediately; is retained by the soil, later to be evaporated or transpired; or is discharged by overland flow to the surface drainage courses. Most of the water that reaches the surface drainage courses eventually sinks to the zone of saturation or is evaporated. The slope of the water table and the movement of ground water are generally eastward. The depth to water ranges from less than 10 feet in parts of the valley to about 300 feet in the upland areas. In much of the Pine Bluffs lowland, the depth to water is less than 50 feet. Ground water not pumped from wells within the area is discharged by evapotranspiration where the water table is close to the land surface, by outflow into streams, or by underflow eastward beneath the State line. The chemical quality of ground water from the principal sources is remarkably uniform, and the range in concentration of dissolved constituents is narrow. In general, the water is of the calcium bicarbonate type, is hard (hardness as CaC03 is as high as 246 ppm), and contains less than about 400 parts per million of dissolved solids, which is a moderate mineralization. Silica constitutes a large proportion of the dissolved solids. The water is suitable for irrigation and, except for iron in water from some wells that tap the Ogallala formation, meets the drinking water standards of the U.S. Public Health Service for chemical constituents. Because the water is siliceous, alkaline, and hard, it is unsuitable for many industrial uses unless treated.

Water Supply Paper↗

USGS2001

Quality of water in alluvial aquifers in eastern Iowa

The goal of the U.S. Geological Survey (USGS) National Water-Quality Assessment (NAWQA) Program is to assess the status and trends in the quality of the Nation's surface and ground water, and to better understand the natural and human factors affecting water quality. The Eastern Iowa Basins study unit encompasses an area of about 50,500 square kilometers (19,500 square miles) in eastern Iowa and southern Minnesota and is one of 59 study units in the NAWQA program. Land-use studies are an important component of the NAWQA program, and are designed to assess the concentration and distribution of water-quality constituents in recently recharged ground water associated with the most significant land use and hydrogeologic settings within a study unit. The focus of the land-use study in the Eastern Iowa Basins study unit is agricultural and urban land uses and alluvial aquifers. Agriculture is the dominant land use in the study unit. Urban areas, although not extensive, represent important potential source areas of contaminants associated with residential, commercial, and industrial activities. Alluvial aquifers are present throughout much of the study unit, and constitute a major ground-water supply that is susceptible to contamination from land-use activities. Ground-water samples were collected from monitoring wells at 31 agricultural and 30 urban sites in the Eastern Iowa Basins study unit during June-August 1997 to evaluate the effects of land use and hydrogeology on the water quality of alluvial aquifers. Calcium, magnesium, and bicarbonate were the dominant ions in most samples and were likely derived from solution of carbonate minerals (calcite and dolomite) present in alluvial detrital deposits. Tritium-based ages indicate ground water was most likely recharged after the 1950's at all but one sampling site. Agricultural and urban land-use areas have remained relatively stable in the study area since the 1950's, therefore the effects of current land use should be reflected in ground water sampled during this study. Sodium and chloride concentrations were significantly higher in samples from urban areas, where roads are more numerous and road salts may be more frequently applied, than in agricultural areas. Nitrate was detected in 94 percent of samples from agricultural areas and 77 percent of samples from urban areas. Nitrate concentrations were significantly higher in agricultural areas than in urban areas and exceeded the U.S. Environmental Protection Agency maximum contaminant level for drinking water (10 milligrams per liter as N) in 39 percent of samples from agricultural areas. Nitrate concentrations in samples from urban areas did not exceed the maximum contaminant level. Greater usage of fertilizers in agricultural areas most likely contributes to higher nitrate concentrations in samples from those areas. Pesticides were detected in 84 percent of samples from agricultural areas and 70 percent from urban areas. Atrazine and metolachlor were the most frequently detected pesticides in samples from agricultural areas; atrazine and prometon were the most frequently detected pesticides in samples from urban areas. None of the pesticide concentrations exceeded U.S. Environmental Protection Agency maximum contaminant levels or lifetime health advisories for drinking water. Pesticide degradates were detected in 94 percent of samples from agricultural areas and 53 percent from urban areas. Metolachlor ethane sulfonic acid and deethylatrazine were the most frequently detected metabolites in samples from agricultural areas; metolachlor ethane sulfonic acid and alachlor ethane sulfonic acid were the most frequently detected degradates in samples from urban areas. Total degradate concentrations were significantly higher in samples from agricultural areas than in samples from urban areas. Total pesticide concentrations (parent compounds) tended to be higher in samples from agricultural areas; however, this difference was not statistically significant. Degradates constituted the major portion of the total residue concentration in the alluvial aquifer. Volatile organic compounds were detected in 40 percent of samples from urban areas and 10 percent from agricultural areas. Methyl tert-butyl ether was the most commonly detected volatile organic compound and was present in 23 percent of samples from urban areas. Elevated concentrations (greater than 30 micrograms per liter) of methyl tert-butyl ether and BTEX compounds (benzene, toluene, ethylbenzene, and xylene) in two samples from urban areas suggest the possible presence of point-source gasoline leaks or spills. Factors other than land use may contribute to observed differences in water quality between and within agricultural and urban areas. Nitrate, atrazine, deethylatrazine, and deisopropylatrazine concentrations were significantly higher in shallow wells with sample intervals nearer the water table and in wells with thinner cumulative clay thickness above the sample intervals, suggesting that longer flow paths allow for greater residence time and increase opportunities for sorbtion, degradation, and dispersion which may contribute to decreases in nutrient and pesticide concentrations with depth. Nitrogen speciation was influenced by redox conditions. Nitrate concentrations were significantly higher in ground water with dissolved-oxygen concentrations in excess of 0.5 milligrams per liter. Ammonia concentrations were higher in ground water with dissolved-oxygen concentrations of 0.5 milligrams per liter or less, however, this relation was not statistically significant. The amount of available organic matter may limit denitrification rates. Elevated nitrate concentrations (greater than 2.0 mg/L) were significantly related to lower dissolved organic carbon concentrations in water samples from both agricultural and urban areas. A similar relation between nitrate concentrations (in water) and organic carbon concentrations (in aquifer material) also was observed but was not statistically significant.

Iowa↗

USGS2000

Effects of land use and hydrogeology on the water quality of alluvial aquifers in eastern Iowa and southern Minnesota, 1997

Ground-water samples were collected from monitoring wells at 31 agricultural and 30 urban sites in the Eastern Iowa Basins study unit during June–August 1997 to evaluate the effects of land use and hydrogeology on the water quality of alluvial aquifers. Ground-water samples were analyzed for common ions, nutrients, dissolved organic carbon, tritium, radon-222, pesticides and pesticide metabolites, volatile organic compounds, and environmental isotopes. Calcium, magnesium, and bicarbonate were the dominant ions in most samples and were likely derived from solution of carbonate minerals (calcite and dolomite) present in alluvial detrital deposits. Chloride and nitrate were dominant anions in samples from several wells. Sodium and chloride concentrations were significantly higher in samples from urban areas, where roads are more numerous and road salts may be more frequently applied, than in agricultural areas. Nitrate was detected in 94 percent of samples from agricultural areas and 77 percent of samples from urban areas. Nitrate concentrations were significantly higher in agricultural areas than in urban areas and exceeded the U.S. Environmental Protection Agency maximum ontaminant level for drinking water (10 milligrams per liter as N) in 39 percent of samples from agricultural areas. Nitrate concentrations in samples from urban areas did not exceed the maximum contaminant level. Greater use of fertilizers in agricultural areas most likely contributes to higher nitrate concentrations in samples from those areas. Tritium-based ages indicate ground water was most likely recharged after the 1950’s at all but one sampling site. Agricultural and urban land-use areas have remained relatively stable in the study area since the 1950’s; therefore, the effects of current land use should be reflected in ground water sampled during this study. Radon-222 was detected in all samples and exceeded the U.S. Environmental Protection Agency’s previously proposed maximum contaminant level for drinking water (300 picocuries per liter) in 71 percent of samples. Pesticides were detected in 84 percent of samples from agricultural areas and 70 percent from urban areas. Atrazine and metolachlor were the most frequently detected pesticides in samples from agricultural areas; atrazine and prometon were the most frequently detected pesticides in samples from urban areas. None of the pesticide oncentrations exceeded U.S. Environmental Protection Agency maximum contaminant levels or lifetime health advisories for drinking water. Pesticide metabolites were detected in 94 percent of samples from agricultural areas and 53 percent from urban areas. Metolachlor ethane sulfonic acid and deethylatrazine were the most frequently detected metabolites in samples from agricultural areas; metolachlor ethane sulfonic acid and alachlor ethane sulfonic acid were the most frequently detected metabolites in samples from urban areas. Total metabolite concentrations were significantly higher in samples from agricultural areas than in samples from urban areas. Total pesticide concentrations (parent compounds) tended to be higher in samples from agricultural areas; however, this difference was not statistically significant. Metabolites constituted the major portion of the total residue concentration in the alluvial aquifer. Volatile organic compounds were detected in 40 percent of samples from urban areas and 10 percent from agricultural areas. Methyl tertbutyl ether was the most commonly detected volatile organic compound and was present in 23 percent of samples from urban areas. Elevated concentrations (greater than 30 micrograms per liter) of methyl tert-butyl ether and BTEX compounds (benzene, toluene, ethylbenzene, and xylene) in two samples from urban areas suggest the possible presence of point-source gasoline leaks or spills. Factors other than land use may contribute to observed differences in water quality between and within agricultural and urban areas. Nitrate, atrazine, deethylatrazine, and deisopropylatrazine concentrations were significantly higher in shallow wells with sample intervals nearer the water table and in wells with thinner cumulative clay thickness above the sample intervals. These relations suggest that longer flow paths allow for greater residence time and increase opportunities for sorption, degradation, and dispersion, which may contribute to decreases in nutrient and pesticide concentrations with depth. Nitrogen speciation was influenced by redox conditions. Nitrate concentrations were significantly higher in ground water with dissolved-oxygen concentrations in excess of 0.5 milligram per liter. Ammonia concentrations were higher in ground water with dissolved-oxygen concentrations of 0.5 milligram per liter or less; however, this relation was not statistically significant. The amount of available organic matter may limit denitrification rates. Elevated nitrate concentrations (greater than 2.0 mg/L) were significantly related to lower dissolved organic carbon concentrations in water samples from both agricultural and urban areas. A similar relation between nitrate concentrations (in water) and organic carbon concentrations (in aquifer material) also was observed but was not statistically significant.

Iowa, Minnesota↗

USGS1997

Variations in pore-water quality, mineralogy, and sedimentary texture of clay-silts in the lower Miocene Kirkwood Formation, Atlantic City, New Jersey

Properties of and pore-water solute chemistry in confining units in the New Jersey Coastal Plain were studied to determine whether leakage of solute-enriched pore water from confining units affects regional aquifer-water chemistry, which ultimately may result in aquifer waters with high sodium and bicarbonate concentrations. Pore-water samples collected from a continuously cored borehole in the lower Miocene Kirkwood Formation at Atlantic City, NJ, were analyzed: 15 samples were obtained from clay-silt confining-unit sediments, and four samples were from silt interbeds in the sand of the major confined aquifer in the region, the Atlantic City 800-ft sand. The samples were analyzed to assess interrelations among mineralogy, texture, fluidretention properties, sediment chemistry, and pore-water chemistry, and to document the scale of variation in these properties. Linear regressions were developed to describe the relations of constituents dissolved in 14 pore-water samples collected from the lower confining unit overlying the Atlantic City 800-ft sand and from the silt interbeds in the upper sand unit of the Atlantic City 800-ft sand. The regressions were for concentrations of magnesium and calcium (m = 0.27, R2 = 0.99); concentrations of sodium and the sum of calcium and magnesium (m = 0.17, R 2 = 0.92); concentrations of sulfate and the sum of calcium and magnesium (m = 1.14, R 2 = 0.99); and concentrations of sodium and sulfate (m = 0.14, R 2 = 0.89). The percentage of fine sand was greatest in the shallowest sampled interval, where pore-water concentrations of calcium, magnesium, and sulfate were greatest. The pore-water samples were of three distinct water-quality types (hydrogeochemical facies): a calcium-sulfate type, a mixed calcium-sodium-sulfate-chloride-bicarbonate type, and a sodium-sulfate-bicarbonate-chloride type. The first two types were found only in the lower confining unit; the third type was found only in the composite confining unit underlying the Atlantic City 800-ft sand. Each of these hydrogeochemical facies generally is found within distinct intervals over a range of tens of feet in the core. Krige estimates of pore-water–constituent variations with depth were made by using only the analytical results for the 14 samples from the lower confining unit overlying the Atlantic City 800-ft sand and the silt interbeds in the upper sand unit of the Atlantic City 800-ft sand. Geostatistical analysis of the pore-water–quality data generally resulted in two types of semivariograms. One semivariogram type best fits concentration trends with depth for calcium, magnesium, strontium, sodium, sulfate, and specific conductance; lithium and chloride may also fit this semivariogram type. The other semivariogram type best fits concentration trends with depth for silica, cation exchange capacity, and dissolved inorganic carbon. The scale of variation of the concentrations and properties is indicated by the maximum lag autocorrelation distance of the theoretical semivariograms (the range) and ranged from 44 to 110 ft (13.4–33.5 m). The scale of variation of pore-water major-ion concentrations of sulfate, chloride, calcium, and magnesium alone is on the order of 65–70 ft (19.8–21.3 m). The semivariograms for all pore-water constituents except silica have significant variance at the smallest lag distance, indicating that the constituent concentration varied over a larger scale than the sampling interval. The dominant exchangeable cation in the sediment is calcium. Cation exchange reactions do not appear to be the dominant process in the sediments of the lower confining unit above the Atlantic City 800-ft sand, because a linear correlation exists between the concentration of sodium and the sum of calcium and magnesium concentrations in the pore water; concentrations of all these constituents increase in the upward flow direction, and the ratio of sodium to chloride in the pore water is about 1.0. Two significant principal components explained 82.5% of the total variation in pore-water solute chemistry. Principal component 1 represents about 53% of the variation in pore-water quality and includes calcium, magnesium, sulfate, strontium, and lithium. Coupled chemical processes in the confining units, such as incongruent dissolution of carbonate and other mineral phases or redox transformations of sulfur, likely explain the covariance of these constituents. Principal component 2 represents about 30% of the variation and includes sodium, dissolved inorganic carbon, and chloride. Covariance of sodium and chloride probably is caused by the presence of residual seawater.

New Jersey↗