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Research about Oklahoma

Source-linked reports with geographic coverage including Oklahoma.

At least 307 records · Page 17Linked to original sources

Effects of municipal ground-water withdrawals on the Arbuckle-Simpson aquifer, Pontotoc County, Oklahoma

The Arbuckle-Simpson aquifer in south-central Oklahoma consists of a thick sequence of folded and faulted carbonate and clastic rocks of Upper Cambrian to Middle Ordovician age. Fractures and karst features locally increase the aquifer's capacity to transmit and store ground water. The aquifer is a principal source of water for municipal and rural users. A hydrologic study was conducted to evaluate the effects of municipal ground-water withdrawal from the Arbuckle-Simpson aquifer on local ground-water levels and discharge from nearby springs and streams in south-central Pontotoc County. A municipal well was pumped for 63 hours at an average rate of 1,170 gallons per minute. A maximum observed drawdown of 0.3 feet was recorded half a mile from the pumping well. Drawdown was observed as far as 1.2 miles from the pumping well. No measurable response was observed at any of the surface-water-discharge measurement sites; however, recharge from precipitation may have masked any decreases in discharge caused by the pumping. Simultaneous pumping of two municipal wells for 241 hours at average rates of 1,170 and 2,730 gallons per minute resulted in a maximum observed drawdown of 1.3 feet recorded at an average distance of 0.80 miles from the pumping wells. The most distant drawdown observed was at an average distance 1.1 miles from the pumped wells. Less that 2 days after pumping stopped, increases in springflow were recorded at two springs; it is unknown whether these discharge responses reflect the effects of recharge from precipitation, or the combined effects of precipitation and the cessation of ground-water withdrawal. The effects of the stress tests on the hydrologic system were offset by recharge from concurrent precipitation. The maximum observed drawdown represents about 6 percent of the median natural water-level fluctuation during the study period. The effect of drawdown could become critical during extended periods of low precipitation, if water levels are already near the bottom of domestic wells in the area. However, a comparison of maximum observed drawdown (1.3 ft) with the minimum saturated thickness of fresh ground water (1,500 ft) suggests that municipal pumping had little effect on the amount of ground water stored in the Arbuckle-Simpson aquifer in the study area. This evaluation is based on the limited pumping rates and times of the stress tests.

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Hydrogeology of the Chickasaw National Recreation Area, Murray County, Oklahoma

The Travertine District (Park) of the Chickasaw National Recreation Area, operated and maintained by the National Park Service, is near the City of Sulphur in south-central Oklahoma. The Park was established in 1902 because of its unique hydrologic setting, which includes Rock Creek, Travertine Creek, numerous mineralized and freshwater springs, and a dense cover of riparian vegetation. Since the turn of the century several flowing artesian wells have been drilled within and adjacent to the Park. Discharge from many of these springs and the numbers of flowing wells have declined substantially during the past 86 years. To determine the cause of these declines, a better understanding of the hydrologic system must be obtained. The U.S. Geological Survey, in cooperation with the National Park Service, has appraised hydrologic information obtained for the Park from several studies conducted during 1902-87. The principal geologic units referred to in this report are the Arbuckle Group and the overlying Simpson Group. These rocks are of Upper Cambrian to Middle Ordovician age and are composed of dolomitic limestone, with some sandstones and shales in the Simpson Group. Surface geologic maps give a general understanding of the regional subsurface geology, but information about the subsurface geology within the Park is poor. The Simpson and Arbuckle aquifers are the principal aquifers in the study area. The two aquifers are not differentiated readily in some parts of the study area because of the similarity of the Simpson and Arbuckle rocks; thus, both water-bearing units are referred to frequently as the Arbuckle-Simpson aquifer. The aquifers are confined under the Park, but are unconfined east and south of the Park. Precipitation on the outcrop area of the Arbuckle aquifer northeast and east of the Park recharges the freshwater springs (Antelope and Buffalo Springs) near the east boundary of the Park. The source of water from mineralized springs located in the central part of the Park, and flowing wells within and north of the Park, is believed to be a mix of waters from rocks of the Arbuckle and Simpson Groups. The source of water from two highly mineralized springs, Bromide and Medicine, that ceased to flow in the early 1970’s is believed to be from the Simpson Group. Water-quality characteristics reflect the sources of ground water in the study area. The highly mineralized springs near the western end of the Park are a sodium chloride type with dissolved solids greater than 4,500 mg/L. The freshwater springs near the eastern end of the Park are a calcium bicarbonate type with total dissolved solids of less than 400 mg/L. Flow from the artesian wells has declined substantially during the past 86 years and the wells are estimated to currently discharge only about 10 percent of the total flow reported in 1939. The depletion is believed to be caused by a gradual lowering of the hydraulic head within the aquifer. The influence on the hydrologic system of local municipal and industrial pumping from the Arbuckle-Simpson aquifer is difficult to discern because the system is much more sensitive to precipitation than to pumpage. Ground-water levels and spring flows in this region respond rapidly to precipitation. The effects of withdrawals from the City of Sulphur and Oklahoma Gas and Electric Company power-plant water-well fields are not discernible at wells and springs. The hydrologic system may be influenced by pumping, particularly during extended dry periods of several years, but the impact of pumping on the system cannot be determined without further investigation.

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Parathion poisoning of Mississippi kites in Oklahoma

Parathion(phosphorothioic acid O, O-diethyl O-[4-nitrophenyl] ester) is a broad spectrum organophosphorus insecticide, used on a variety of crops and occasionally for mosquito control, and is highly toxic to birds (Smith 1987). Intentional poisoning with parathion is reported to have killed more than 8000 red-winged blackbirds (Agelaius phoeniceus), common grackles (Quiscalus quiscula), brown-headed cowbirds (Molothrus ater) and European starlings (Sturnus vulgaris) in two separate instances (Stone et al. 1984). Use of parathion on wheat fields has resulted in the mortality of about 1600 Canada geese (Branta canadensis) and other waterfowl in one instance (White et al. 1982) and about 200 Canada geese in another (Flickinger et al. 1991). More than 200 laughing gulls (Larus atricilla) died near cotton fields treated with parathion (White et al. 1979). Secondary poisoning of raptors resulting from the consumption of prey exposed to parathion, has been reported experimentally and in the field. Stone et al. (1984) found two dead red-tailed hawks (Buteo jamaicensis), a Cooper's hawk (Accipiter cooperii) and an American kestrel (Falco sparverius) that had fed on blackbirds killed by parathion. One of four American kestrels died after being fed cricket frogs (Acris crepitans) that had been exposed to 10ppm parathion for 96 hr (Fleming et al. 1982). The Mississippi kite (Ictinia mississippensis) is highly insectivorous (Brown and Amadon 1968) and is thus subject to secondary poisoning resulting from consumption of insects exposed to pesticides. I report here an instance of secondary parathion poisoning in wild Mississippi kites.

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Nature of migrabitumen and their relation to regional thermal maturity, Ouachita Mountains, Oklahoma

Two grahamite and three impsonite localities are within an 82-km-long segment of the Ouachita Mountains of southeastern Oklahoma. Grab samples were collected to study the petrographic and geochemical characteristics of the migrabitumen at the grahamite-impsonite transition and the relation of the migrabitumen to the regional thermal maturity pattern. Maximum and random bitumen reflectance values increased from 0·75 to 1·80% from west to east, consistent with the regional thermal maturation trend. Mean bireflectance values increased from 0·04 to 0·38%. The two grahamite samples are classified at the grahamite-impsonite boundary with conflicting petrographic (bitumen reflectance) and bulk chemical (volatile matter) maturity indicators. The regional maturation trend, based on vitrinite reflectance and bitumen reflectance values, was confirmed by a detailed geochemical investigation of bitumen extracts. Although biomarker analyses were influenced by extensive biodegradation effects, molecular parameters based on the phenanthrenes, dibenzothiophenes, and tricyclic terpanes were identified as useful maturity indicators.

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Ground-water-quality assessment of the Central Oklahoma Aquifer, Oklahoma: Geochemical and geohydrologic investigations

The National Water-Quality Assessment pilot project for the Central Oklahoma aquifer examined the chemical and isotopic composition of ground water, the abundances and textures of minerals in core samples, and water levels and hydraulic properties in the flow system to identify geochemical reactions occurring in the aquifer and rates and directions of ground-water flow. The aquifer underlies 3,000 square miles of central Oklahoma and consists of Permian red beds, including parts of the Permian Garber Sandstone, Wellington Formation, and Chase, Council Grove, and Admire Groups, and Quaternary alluvium and terrace deposits. In the part of the Garber Sandstone and Wellington Formation that is not confined by the Permian Hennessey Group, calcium, magnesium, and bicarbonate are the dominant ions in ground water; in the confined part of the Garber Sandstone and Wellington Formation and in the Chase, Council Grove, and Admire Groups, sodium and bicarbonate are the dominant ions in ground water. Nearly all of the Central Oklahoma aquifer has an oxic or post-oxic environment as indicated by the large dissolved concentrations of oxygen, nitrate, arsenic(V), chromium(VI), selenium(VI), vanadium, and uranium. Sulfidic and methanic environments are virtually absent. Petrographic textures indicate dolomite, calcite, sodic plagioclase, potassium feldspars, chlorite, rock fragments, and micas are dissolving, and iron oxides, manganese oxides, kaolinite, and quartz are precipitating. Variations in the quantity of exchangeable sodium in clays indicate that cation exchange is occurring within the aquifer. Gypsum may dissolve locally within the aquifer, as indicated by ground water with large concentra-tions of sulfate, but gypsum was not observed in core samples. Rainwater is not a major source for most elements in ground water, but evapotranspiration could cause rainwater to be a significant source of potassium, sulfate, phosphate and nitrogen species. Brines derived from seawater are the most likely source of bromide and chloride in the aquifer. The dominant reaction in recharge is the uptake of carbon dioxide gas from the unsaturated zone (about 2.0 to 4.0 millimoles per liter) and the dissolution of dolomite (about 0.3 to 1.0 millimoles per liter). This reaction generates calcium, magnesium, and bicarbonate water composition. If dolomite does not dissolve to equilibrium, pH values range from 6.0 to 7.3; if dolomite dissolves to equilibrium, pH values are about 7.5. By the time recharge enters the deeper flow system, all ground water is saturated or supersaturated with dolomite and calcite. After carbonate-mineral equilibration has occurred, cation exchange of calcium and magnesium for sodium is the dominant geochemical reaction, which occurs to a substantial extent only in parts of the aquifer. Mass transfers of cation exchange greater than 2.0 millimoles per liter occur in the confined part of the Garber Sandstone and Wellington Formation and in parts of the Chase, Council Grove, and Admire Groups. Associated with cation exchange is dissolution of small quantities of dolomite, calcite, biotite, chlorite, plagioclase, or potassium feldspar, which produces pH values that range from 8.6 to 9.1. Large tritium concentrations indicate ground-water ages of less than about 40 years for most samples of recharge. Carbon-14 ages for samples from the unconfined aquifer generally are less than 10,000 years. Carbon-14 ages of ground water in the confined part of the aquifer range from about 10,000 to 30,000 years or older. These ages produce a time trend in deuterium values that qualitatively is consistent with the timing of the transition from the last glacial maximum to the present interglacial period. The most transmissive geologic units in the Central Oklahoma aquifer are the Garber Sandstone and Wellington Formation and the alluvium and terrace deposits; the Chase, Council Grove, and Admire Groups are less transmissive on the basis of available specific-capacity data. The transmissivities of the Permian geologic units depend largely on the percentage of sandstone; the percentage is greatest in the central part of the aquifer and decreases in all directions from this central part. Because of large mudstone and siltstone contents, the Hennessey Group and the Vanoss Formation are assumed to be confining units above and below the aquifer. The Cimarron and Canadian Rivers are defined to be the northern and southern extent of the aquifer because of decreases in transmissivity beyond the rivers and because there is no indication of ground-water underflow at these rivers. The eastern boundary of the aquifer is the limit of the outcrop of the Chase, Council Grove, and Admire Groups. The presence of brines in the western part of the study unit and below the aquifer indicate the extent of the freshwater flow system in these directions. Regional ground-water flow is west to east; the Deep Fork is a major discharge area for the regional flow system. Local flow systems are present within the unconfined part of the study unit. Most streams are gaining streams, and very few losing streams are evident. Median values of aquifer properties were estimated as follows: recharge to the saturated zone, 1.6 inches per year; evapotranspiration of water that never reaches the saturated zone, 25 to 30 inches per year; porosity, 0.22; storage coefficient, 0.0002; transmissivity, 260 to 450 feet squared per day; horizontal hydraulic conductivity, 4.5 feet per day; and the ratio of horizontal to vertical hydraulic conductivity, 10,000. Reported ground-water withdrawals peaked in 1985 at 13,900 million gallons but had decreased to 7,860 million gallons by 1989. Unreported domestic withdrawals were estimated to be 1,685 million gallons in 1980. The flow system in the aquifer can be considered to have three major components: (1) A shallow, local flow system in the unconfined part of the aquifer, (2) a deep, regional flow system in the unconfined part of the aquifer, and (3) a deep, regional flow system in the confined part of the aquifer. In the shallow, local flow system, water flows relatively quickly along short flowlines from the point of recharge to the point of discharge at the nearest stream. Many water samples from shallow wells contain large concentrations of tritium, which indicate ground-water ages of less than 40 years. In the deep, regional flow system in the unconfined part of the aquifer, water takes more time to flow along longer flowlines than in the shallow, local flow system. Much of the water in this flow system is recharged along ridges that correspond to ground-water divides between drainage basins. Transit times for water recharging the aquifer along ridges is greater than 5,000 years, computed using a numerical flow model in conjunction with a particle-tracking model. The deep, regional flow system in the confined part of the Garber Sandstone and Wellington Formation is recharged from a small part of the outcrop area of the Garber Sandstone. From the recharge area, water flows west under the confining unit to discharge to streams as far away as the Cimarron River. Flowpaths are relatively long, as much as 50 miles. The transit times in this flow system range from thousands to tens of thousands of years. The long-term hydrogeochemical process occurring in the Central Oklahoma aquifer is removal of unstable minerals, including dolomite, calcite, biotite, chlorite, and feldspars, and the replacement of exchangeable sodium on clays with calcium and magnesium. Over geologic time, the flux of water through the rapidly moving, local flow system has been sufficient to remove most of the dolomite, calcite, and exchangeable sodium. In places, chlorite and feldspars have been removed. In the deep, regional flow system of the unconfined part of the Garber Sandstone and Wellington Formation, the flux of water has been sufficient to remove most of the exchangeable sodium, but carbonate minerals remain sufficiently abundant to maintain dolomite and calcite equilibrium. In the confined part of the Garber Sandstone and Wellington Formation and in the less transmissive parts of the unconfined aquifer, including the Chase, Council Grove, and Admire Groups, ground-water flow is slowest, and the flux of water and extent of reaction have been insufficient to remove either the carbonate minerals or the exchangeable sodium on clays.

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Hydrogeologic maps of the central Oklahoma aquifer, Oklahoma

This report presents hydrogeologic maps of the Central Oklahoma aquifer. The maps were prepared by measuring water levels in wells during the winder of 1986 and 1987; examination of geophysical logs to determine the altitudes of the top of selected geologic units and the base of fresh ground water; and compilation of existing information on the stratigraphy of selected geologic units and the base of fresh ground water.

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Ground-water-quality assessment of the central Oklahoma aquifer, Oklahoma: Hydrologic, water-quality, and quality-assurance data 1987-90

This report presents data collected from 202 wells between June 1987 and September 1990 as part of the Central Oklahoma aquifer pilot study of the National Water-Quality Assessment Program. The report describes the sampling networks, the sampling procedures, and the results of the ground-water quality and quality-assurance sample analyses. The data tables consist of information about the wells sampled and the results of the chemical analyses of ground water and quality-assurance sampling. Chemical analyses of ground-water samples in four sampling networks are presented: A geochemical network, a low-density survey bedrock network, a low-density survey alluvium and terrace deposits network, and a targeted urban network. The analyses generally included physical properties, major ions, nutrients, trace substances, radionuclides, and organic constituents. The chemical analyses of the ground-water samples are presented in five tables: (1) Physical properties and concentrations of major ions, nutrients, and trace substances; (2) concentrations of radionuclides and radioactivities; (3) carbon isotope ratios and delta values (d-values) of selected isotopes; (4) concentrations of organic constituents; and (5) organic constituents not reported in ground-water samples. The quality of the ground water sampled varied substantially. The sum of constituents (dissolved solids) concentrations ranged from 71 to 5,610 milligrams per liter, with 38 percent of the wells sampled exceeding the Secondary Maximum Contaminant Level of 500 milligrams per liter established under the Safe Drinking Water Act. Values of pH ranged from 5.7 to 9.2 units with 20 percent of the wells outside the Secondary Maximum Contaminant Level of 6.5 to 8.5 units. Nitrite plus nitrate concentrations ranged from less than 0.1 to 85 milligrams per liter with 8 percent of the wells exceeding the proposed Maximum Contaminant Level of 10 milligrams per liter. Concentrations of trace substances were highly variable, ranging from below the reporting level to concentrations over the Maximum Contaminant Levels for several constituents (arsenic, barium, cadmium, chromium, lead, and selenium). Radionuclide activities also were highly variable. Gross alpha radioactivity ranged from 0.1 to 210 picocuries per liter as 230thorium. Of the wells sampled, 20 percent exceeded the proposed Maximum Contaminant Level of 15 picocuries per liter for gross alpha radioactivity. Organic constituents were detected in 39 percent of the 170 wells sampled for organic constituents; in most cases concentrations were at or near the laboratory minimum reporting levels. Ten of the wells sampled for organic constituents had one or more constituents (chlordane, dieldrin, heptachlor epoxide, trichloroethylene, 1,1-dichloroethylene, 1,1,1-trichloroethane) at concentrations equal to or greater than the Maximum Contaminant Level or acceptable concentrations as suggested in the Environmental Protection Agency's Health Advisory Summaries. Quality-assurance sampling included duplicate samples, repeated samples, blanks, spikes, and blind samples. These samples proved to be essential in evaluating the accuracy of the data, particularly in the case of volatile organic constituents.

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Water Resources Data, Oklahoma, Water Year 1991

Water resources data for the 1991 water year for Oklahoma consists of records of stage, discharge, and water quality of streams; stage, contents, and water quality of lakes or reservoirs; and water levels of ground-water wells. This report contains discharge records for 131 gaging stations; stage and contents for 30 lakes or reservoirs; water quality for 46 gaging stations and 2 lakes. Also included are 11 partial-record stations and 27 ground-water sites. These data represent that part of the National Water Data System collected by the U.S. Geological Survey and cooperating State and Federal agencies in Oklahoma.

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A comparison of short-term measurements of lake evaporation using eddy correlation and energy budget methods

Concurrent short-term measurements of evaporation from a shallow lake, using eddy correlation and energy budget methods, indicate that sensible and latent heat flux between lake and atmosphere, and energy storage in the lake, may vary considerably across the lake. Measuring net radiation with a net radiometer on the lake appeared to be more accurate than measuring incoming radiation nearby and modeling outgoing radiation. Short-term agreement between the two evaporation measurements was obtained by using an energy storage term that was weighted to account for the area-of-influence of the eddy correlation sensors. Relatively short bursts of evaporation were indicated by the eddy correlation sensors shortly after midnight on two of three occasions.

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Organic petrology of epi-impsonite at Page, Oklahoma, U.S.A.

Impsonite (asphaltic pyrobitumen) occurs as fracture-filling veins cutting massive sandstone in the frontal Ouachita Mountains near Page, Oklahoma. The Page impsonite formed from low-temperature alteration of crude oil. Mean maximum bitumen reflectance in oil immersion ( R max "> R max ) of seven samples is 1.41–1.96%. Mean apparent bireflectance of these samples is 0.15–0.54%. The Page deposit classifies at the upper end of epi-impsonite in the generic classification for solid bitumen, based on physical, chemical, and optical characteristics, and as post-oil with unlimited migration in the genetic classification for solid bitumen.

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Ore microscopy of the Paoli silver-copper deposit, Oklahoma

The Paoli silver-copper deposit is located in south-central Oklahoma, 56 km south-southeast from Norman, Oklahoma. It was mined for high-grade silver-copper near the beginning of this century, and intensive exploratory drilling during the early 1970's delineated unmined portions of the deposit. A collaborative study between the U.S.G.S., the Kansas Geological Survey, and the University of Missouri-Rolla was undertaken to provide new information on the character of red bed copper deposits of the Midcontinent region. The Paoli deposit has been interpreted to occur as a roll-front type of deposit. The silver and copper mineralization occurs within paleochannels in the Permian Wellington Formation. The silver-copper interfaces appear to be controlled by oxidation-reduction interfaces that are marked by grey to red color changes in the host sandstone. Ore microscopic examinations of polished thin sections show that unoxidized ore consists of chalcocite, digenite, chalcopyrite, covellite and pyrite; and oxidized ores are characterized by covellite, bornite, hematite and goethite. In sandstone-hosted ores, chalcocite and digenite replace dolomite and border clastic quartz grains. In siltstone-hosted ores, the copper sulfide grains have varied shapes; most are irregular in shape and 5–25 μm across, others have euhedral shapes suggestive of pyrite crystal replacements, and some are crudely spherical and are 120–200 μm across. Chalcopyrite is the predominant copper sulfide at depth. Covellite and malachite replace chalcocite and digenite near the surface. Silver only occurs as native silver; most as irregularly shaped grains 40–80 μm across, but some as cruciform crystals that are up to 3.5 mm across. The native silver has been deposited after copper sulfides, and locally replaces chalcocite. Surficial nodules of pyrite, malachite and hematite locally are present in outcrops at the oxidation-reduction fronts. Polished sections of the nodules show that malachite forms a cement around quartz sand grains, and brecciated pyrite grains are surrounded by rims of hematite and goethite. Dolomite is the principal sandstone cement. Cathodoluminescence microscopic study of the mineral has shown that it was deposited during seven periods before the copper sulfide mineralization.

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