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Scott Christenson

Publications and source records attributed to Scott Christenson.

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Hydrogeology and simulation of groundwater flow in the Arbuckle-Simpson aquifer, south-central Oklahoma

The Arbuckle-Simpson aquifer in south-central Oklahoma provides water for public supply, farms, mining, wildlife conservation, recreation, and the scenic beauty of springs, streams, and waterfalls. Proposed development of water supplies from the aquifer led to concerns that large-scale withdrawals of water would cause decreased flow in rivers and springs, which in turn could result in the loss of water supplies, recreational opportunities, and aquatic habitat. The Oklahoma Water Resources Board, in collaboration with the Bureau of Reclamation, the U.S. Geological Survey, Oklahoma State University, and the University of Oklahoma, studied the aquifer to provide the Oklahoma Water Resources Board the scientific information needed to determine the volume of water that could be withdrawn while protecting springs and streams. The U.S. Geological Survey, in coopertion with the Oklahoma Water Resources Board, did a study to describe the hydrogeology and simulation of groundwater flow of the aquifer. The outcrop of the Arbuckle-Simpson aquifer covers an area of about 520 square miles in Carter, Coal, Johnston, Murray, and Pontotoc Counties. Three subdivisions of the aquifer outcrop were designated for this study: the eastern, central, and western Arbuckle-Simpson aquifer. This study emphasized the eastern Arbuckle-Simpson aquifer because it is the largest part of the aquifer by area and volume; most groundwater withdrawals are from the eastern Arbuckle-Simpson aquifer; and the largest (by flow) streams and springs sourced from the aquifer are on the eastern Arbuckle-Simpson aquifer. The aquifer lies in an uplifted area commonly referred to as the Arbuckle Mountains, which is characterized by great thicknesses of mostly carbonate rocks, uplifts, folded structures, and large fault displacements. The Arbuckle-Simpson aquifer is contained in three major rock units of Late Cambrian to Middle Ordovician age: the Timbered Hills, Arbuckle, and Simpson Groups. The aquifer is underlain by low-permeability Cambrian and Proterozoic igneous and metamorphic rocks, and is confined above by younger sedimentary rocks of various ages in areas where the top of the aquifer dips below the surface. The major part of the Arbuckle-Simpson aquifer is the Arbuckle Group, which consists of as much as 6,700 feet of limestone in the western Arbuckle-Simpson aquifer, but which thins to an estimated 3,000 feet of predominantly dolostone in the eastern Arbuckle-Simpson aquifer. Water is obtained from cavities, solution channels, fractures, and intercrystalline porosity in the limestone and dolostone. The overlying Simpson Group, consisting of sandstones, shales, and limestones, is as much as 2,300 feet thick in the western Arbuckle-Simpson aquifer, but generally is less than 1,000 feet thick in the eastern aquifer. Water in the Simpson Group is stored primarily in pore spaces between the sand grains in the sandstones. A digital, three-dimensional geologic framework model was constructed to define the geometric relations of fault blocks and subsurface rock units across complex fault zones of the eastern Arbuckle-Simpson aquifer. Geologic data for the model were obtained from 126 drill holes; stratigraphic contacts and faults defined from a digitized version of the surface geologic map; and fault geometry, stratigraphic thickness, and information compiled from geologic and hydrogeologic reports and maps. Groundwater in the aquifer moves from areas of high head (altitude) to areas of low head along streams and springs. The potentiometric surface in the eastern Arbuckle-Simpson aquifer generally slopes from a topographic high from northwest to the southeast, indicating that regional groundwater flow is predominantly toward the southeast. Freshwater is known to extend beyond the aquifer outcrop near the City of Sulphur, Oklahoma, and Chickasaw National Recreation Area, where groundwater flows west from the outcrop of the eastern Arbuckle-Simpson aquifer and becomes confin

Scientific Investigations Report

Stable-isotope ratios of hydrogen and oxygen in precipitation at Norman, Oklahoma, 1996–2008

Precipitation samples for measurement of stable-isotope ratios of hydrogen (delta 2 H) and oxygen (delta 18 O) were collected at the Norman Landfill Research Site in Norman, Oklahoma, from May 1996 to October 2008. Rainfall amounts also were measured at the site (U.S. Geological Survey gaging station 07229053) during the collection period. The delta 2 H of precipitation samples ranged from -121.9 to +8.3 per mil, and the delta 18 O of precipitation ranged from -16.96 to +0.50 per mil. The volume-weighted average values for delta 2 H and delta 18 O of precipitation over the 12-year measurement period were -31.13 per mil for delta 2 H and -5.57 per mil for delta 18 O. Average summer-season delta 2 H and delta 18 O values of precipitation usually were more positive (enriched in the heavier isotopes) than winter values.

Oklahoma

Assessing groundwater availability in the High Plains aquifer in parts of Colorado, Kansas, Nebraska, New Mexico, Oklahoma, South Dakota, Texas, and Wyoming

The U.S. Geological Survey's Groundwater Resources Program is conducting an assessment of groundwater availability to gain a clearer understanding of the status of the Nation's groundwater resources and the natural and human factors that can affect those resources. The goals of this national effort are to define the current status and improve understanding of the Nation's groundwater resources, to better estimate availability and suitability of those resources for use in the future, and to provide tools to estimate the future availability of ground-water for its various uses. Assessments will be completed for regional aquifer systems across the Nation to help characterize how much water we have, where groundwater resources are most stressed, how groundwater availability is changing, and where groundwater resources are most available for future use.

Colorado, Kansas, Nebraska, New Mexico, Oklahoma,

Three-dimensional geologic model of the Arbuckle-Simpson aquifer, south-central Oklahoma

The Arbuckle-Simpson aquifer of south-central Oklahoma encompasses more than 850 square kilometers and is the principal water resource for south-central Oklahoma. Rock units comprising the aquifer are characterized by limestone, dolomite, and sandstones assigned to two lower Paleozoic units: the Arbuckle and Simpson Groups. Also considered to be part of the aquifer is the underlying Cambrian-age Timbered Hills Group that contains limestone and sandstone. The highly faulted and fractured nature of the Arbuckle-Simpson units and the variable thickness (600 to 2,750 meters) increases the complexity in determining the subsurface geologic framework of this aquifer. A three-dimensional EarthVision (Trademark) geologic framework model was constructed to quantify the geometric relationships of the rock units of the Arbuckle-Simpson aquifer in the Hunton anticline area. This 3-D EarthVision (Trademark) geologic framework model incorporates 54 faults and four modeled units: basement, Arbuckle-Timbered Hills Group, Simpson Group, and post-Simpson. Primary data used to define the model's 54 faults and four modeled surfaces were obtained from geophysical logs, cores, and cuttings from 126 water and petroleum wells. The 3-D framework model both depicts the volumetric extent of the aquifer and provides the stratigraphic layer thickness and elevation data used to construct a MODFLOW version 2000 regional groundwater-flow model.

Open-File Report

Geochemistry of the Arbuckle-Simpson Aquifer

The Arbuckle-Simpson aquifer in south-central Oklahoma provides water for public supply, farms, mining, wildlife conservation, recreation, and the scenic beauty of springs, streams, and waterfalls. A new understanding of the aquifer flow system was developed as part of the Arbuckle-Simpson Hydrology Study, done in 2003 through 2008 as a collaborative research project between the State of Oklahoma and the Federal government. The U.S. Geological Survey collected 36 water samples from 32 wells and springs in the Arbuckle-Simpson aquifer in 2004 through 2006 for geochemical analyses of major ions, trace elements, isotopes of oxygen and hydrogen, dissolved gases, and dating tracers. The geochemical analyses were used to characterize the water quality in the aquifer, to describe the origin and movement of ground water from recharge areas to discharge at wells and springs, and to determine the age of water in the aquifer.

Oklahoma

Geochemical investigation of the Arbuckle-Simpson Aquifer, South-Central Oklahoma, 2004-06

A geochemical reconnaissance investigation of the Arbuckle-Simpson aquifer in south-central Oklahoma was initiated in 2004 to characterize the ground-water quality at an aquifer scale, to describe the chemical evolution of ground water as it flows from recharge areas to discharge in wells and springs, and to determine the residence time of ground water in the aquifer. Thirty-six water samples were collected from 32 wells and springs distributed across the aquifer for chemical analysis of major ions, trace elements, isotopes of oxygen and hydrogen, dissolved gases, and age-dating tracers. In general, the waters from wells and springs in the Arbuckle-Simpson aquifer are chemically suitable for all regulated uses, such as public supplies. Dissolved solids concentrations are low, with a median of 347 milligrams per liter (mg/L). Two domestic wells produced water with nitrate concentrations that exceeded the U.S. Environmental Protection Agency's nitrate maximum contaminant level (MCL) of 10 mg/L. Samples from two wells in the confined part of the aquifer exceeded the secondary maximum contaminant level (SMCL) for chloride of 250 mg/L and the SMCL of 500 mg/L for dissolved solids. Water samples from these two wells are not representative of water samples from the other wells and springs completed in the unconfined part of the aquifer. No other water samples from the Arbuckle-Simpson geochemical reconnaissance exceeded MCLs or SMCLs, although not every chemical constituent for which the U.S. Environmental Protection Agency has established a MCL or SMCL was analyzed as part of the Arbuckle-Simpson geochemical investigation. The major ion chemistry of 34 of the 36 samples indicates the water is a calcium bicarbonate or calcium magnesium bicarbonate water type. Calcium bicarbonate water type is found in the western part of the aquifer, which is predominantly limestone. Calcium magnesium bicarbonate water is found in the eastern part of the aquifer, which is predominantly a dolomite. The major ion chemistry for these 34 samples is consistent with a set of water-rock interactions. Rainfall infiltrates the soil zone, where the host rock, limestone or dolomite, dissolves as a result of uptake of carbon dioxide gas. Some continued dissolution of dolomite and precipitation of calcite occur as the water flows through the saturated zone. The major ion chemistry of the two samples from wells completed in the confined part of the aquifer indicates the water is a sodium chloride type. Geochemical inverse modeling determined that mixing of calcite-saturated recharge water with brine and dissolving calcite, dolomite, and gypsum accounts for the water composition of these two samples. One of the two samples, collected at Vendome Well in Chickasaw National Recreation Area, had a mixing fraction of brine of about 1 percent. The brine component of the sample at Vendome Well is likely to account for the relatively large concentrations of many of the trace elements (potassium, fluoride, bromide, iodide, ammonia, arsenic, boron, lithium, selenium, and strontium) measured in the water sample. Carbon-14, helium-3/tritium, and chlorofluorocarbons were used to calculate ground-water ages, recharge temperatures, and mixtures of ground water in the Arbuckle-Simpson aquifer. Thirty four of 36 water samples recharged the aquifer after 1950, indicating that water is moving quickly from recharge areas to discharge at streams and springs. Two exceptions to this classification were noted in samples 6 and 15 (Vendome Well). Ground-water ages determined for these two samples by using carbon-14 are 34,000 years (site 6) and 10,500 years (site 15). Concentrations of dissolved argon, neon, and xenon in water samples were used to determine the temperature of the water when it recharged the aquifer. The mean annual air temperature at Ada, Oklahoma, is 16 degrees Celsius (C) and the median temperature of the 30 reconnaissance water samples was 18.1 C. The av

Oklahoma

Elements in cottonwood trees as an indicator of ground water contaminated by landfill leachate

Ground water at the Norman Landfill Research Site is contaminated by a leachate plume emanating from a closed, unlined landfill formerly operated by the city of Norman, Oklahoma, Ground water contaminated by the leachate plume is known to be elevated in the concentration of many, organic and inorganic constituents. Specific conductance, alkalinity, chloride, dissolved organic carbon, boron, sodium, strontium, and deuterium in ground water are considered to be indicators of the leachate plume at this site. Leaf samples of broad-leafed cottonwood, Populus deltoides, were collected from 57 sites around the closed landfill. Cottonwood, a phreatophyte or “well plant,” functions as a & surrogate well and serves as a ground water quality sampler. The leaf samples were combusted to ash and analyzed by instrumental neutron activation for 35 elements and by prompt-gamma instrumental neutron activation, for boron. A monitoring well was located within a few meters of a sampled cottonwood tree at 15 of the 57 sites, and ground water samples were collected from these monitoring wells simultaneously with a leaf sample. The chemical analyses of the ground water and leaf samples from these 15 sites indicated that boron, bromine, sodium, and strontium concentrations in leaves were significantly correlated with leachate indicator constituents in ground water. A point-plot map of selected percentiles indicated high concentrations of boron, bromine, and sodium in leaf ash from sites downgradient of the most recent landfill and from older landfills nearby. Data from leaf analysis greatly extended the known areal extent of the leachate plume previously determined from a network of monitoring wells and geophysical surveys. This phytosgeochemical study provided a cost-effective method for assessing the extent of a leachate plume from an old landfill. Such a method may be useful as a preliminary sampling tool to guide the design of hydrogeochemical and geophysical studies.

Oklahoma

Naturally Occurring Arsenic in Ground Water, Norman, Oklahoma, 2004, and Remediation Options for Produced Water

In 2000, the U.S. Environmental Protection Agency (EPA) reviewed the arsenic drinking water standard for public water supplies. Considering the available research and statistics on the health effects of arsenic ingestion, the EPA reduced the Maximum Contaminant Level (MCL) for public drinking water from 50 micrograms per liter (?g/L) to 10 ?g/L (U.S. Environmental Protection Agency, 2001a). As a result of the more stringent standard, the EPA estimates that about 3,000 public water providers across the United States must take action to meet the new standard before it becomes effective on January 23, 2006 (U.S. Environmental Protection Agency, 2001b). The City of Norman (City) is one of several Oklahoma municipalities affected by the new arsenic standard. About 20 percent of Norman?s water is supplied by wells completed in the Central Oklahoma (Garber-Wellington) aquifer; the rest is supplied by Lake Thunderbird (fig. 1) or purchased from Oklahoma City. The Norman well field is composed of 24 active wells, and water produced from about half of the wells will not be in compliance with the new MCL (figs. 2 and 3). Chemical treatment of water with elevated arsenic is possible, but it is generally cost prohibitive. Another costly solution is simply to abandon the high-arsenic wells and replace them with new wells in low-arsenic areas. In the next phase of well construction beginning in 2005, the City plans to construct as many as 30 new wells in northeast Norman (Bryan Mitchell, City of Norman, oral commun., 2005). The new wells will replace production lost to the new arsenic standard and add new production to keep pace with rapidly growing consumer demand. Well modification to exclude arsenic-bearing water from existing wells is a more cost-effective solution, but it requires a great deal of knowledge about local aquifer properties and individual well dynamics to decide which wells are good candidates for modification. With the goal of determining if well modification can be used to bring some of Norman?s high-arsenic wells into compliance with the new arsenic standard, the EPA Office of Research and Development (ORD) initiated a three-year research project in 2003 with participation from the U.S. Geological Survey (USGS), Oklahoma State University, and the City of Norman. The primary objectives of the project are to: (1) determine where naturally occurring arsenic is entering wells by collecting water samples at different depths, (2) investigate the utility of new methods for collecting water-quality data in a pumping well, (3) better understand the stratigraphy and composition of aquifer rocks, (4) assess 10 wells for the possibility of arsenic remediation by well modification, and (5) evaluate the effectiveness of well modification in bringing marginal wells into compliance with the new arsenic MCL. The purpose of this report is to describe the occurrence of arsenic in ground water near Norman, Oklahoma, and available options for reducing arsenic concentrations in produced ground water.

Fact Sheet

Recharge processes in an alluvial aquifer riparian zone, Norman Landfill, Norman, Oklahoma, 1998-2000

Analyses of stable isotope profiles (d2H and d18O) in the saturated zone, combined with water-table fluctuations, gave a comprehensive picture of recharge processes in an alluvial aquifer riparian zone. At the Norman Landfill U.S. Geological Survey Toxic Substances Hydrology research site in Norman, Oklahoma, recharge to the aquifer appears to drive biodegradation, contributing fresh supplies of electron acceptors for the attenuation of leachate compounds from the landfill. Quantifying recharge is a first step in studying this process in detail. Both chemical and physical methods were used to estimate recharge. Chemical methods included measuring the increase in recharge water in the saturated zone, as defined by isotopic signature, specific conductance or chloride measurements; and infiltration rate estimates using storm event isotopic signatures. Physical methods included measurement of water-table rise after individual rain events and on an approximately monthly time scale. Evapotranspiration rates were estimated using diurnal watertable fluctuations; outflux of water from the alluvial aquifer during the growing season had a large effect on net recharge at the site. Evaporation and methanogenesis gave unique isotopic signatures to different sources of water at the site, allowing the distinction of recharge using the offset of the isotopic signature from the local meteoric water line. The downward movement of water from large, isotopically depleted rain events in the saturated zone yielded recharge rate estimates (2.2 - 3.3 mm/day), and rates also were determined by observing changes in thickness of the layer of infiltrated recharge water at the top of the saturated zone (1.5 - 1.6 mm/day). Recharge measured over 2 years (1998-2000) in two locations at the site averaged 37 percent of rainfall, however, part of this water had only a short residence time in the aquifer. Isotopes showed recharge water entering the ground-water system in winter and spring, then being removed during the growing season by phreatophyte transpiration. Recharge timing was variable over the course of the study; July and August were the only months that had no recharge in both years. Recharge to the aquifer from the slough (wetland pond) was estimated at one location using the isotopic signature of water affected by evaporation. Recharge was correlated with the rainfall amount over the period of estimation, suggesting that recharge from the slough to the downgradient aquifer was an episodic process, corresponding to elevated water levels in the slough after large rain events.

Oklahoma