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At least 37 records · Page 2Linked to original sources
USGS1999

Chemical composition and geologic history of saline waters in Aux Vases and Cypress Formations, Illinois Basin

Seventy-six samples of formation waters were collected from oil wells producing from the Aux Vases or Cypress Formations in the Illinois Basin. Forty core samples of the reservoir rocks were also collected from the two formations. Analyses of the samples indicated that the total dissolved solids content (TDS) of the waters ranged from 43,300 to 151,400 mg/L, far exceeding the 35,400 mg/mL of TDS found in typical seawater. Cl-Br relations suggested that high salinities in the Aux Vases and Cypress formation waters resulted from the evaporation of original seawater and subsequent mixing of the evaporated seawater with concentrated halite solutions. Mixing with the halite solutions increased Na and Cl concentrations and diluted the concentration of other ions in the formation waters. The elemental concentrations were influenced further by diagenetic reactions with silicate and carbonate minerals. Diagenetic signatures revealed by fluid chemistry and rock mineralogy delineated the water-rock interactions that took place in the Aux Vases and Cypress sandstones. Dissolution of K-feldspar released K into the solution, leading to the formation of authigenic illite and mixed-layered illite/smectite. Some Mg was removed from the solution by the formation of authigenic chlorite and dolomite. Dolomitization, calcite recrystallization, and contribution from clay minerals raised Sr levels significantly in the formation waters. The trend of increasing TDS of the saline formation waters with depth can be explained with density stratification. But, it is difficult to explain the combination of the increasing TDS and increasing Ca/Na ratio with depth without invoking the controversial 'ion filtration' mechanism.

Aquatic Geochemistry↗
USGS1970

Geologic log and chemical data, diamond drill hole 1, Samrah, Kingdom of Saudi Arabia

Diamond drill hole number 1 at the Samrah ancient mine, Kingdom of Saudi Arabia penetrated a series of mineralized fractures. Lead, zinc, and silver are the principal ore metals and galena and sphalerito are the ore minerals identified to date. Throughout the core there is a somewhat better correlation of silver with zinc than with lead. The richest interval of core is in the main vein, 51-1/2 feet of core from 430 to 482 feet, and averages nearly 20 ounces of silver to the ton. Within this interval, 15 feet of core from 444 to 459 feet averages 60 ounces of silver to the ton. The richest single sample represents the five-foot interval from 454 to 459 feet and is reported to contain nearly 140 ounces of silver to the ton. All of these intervals contain recoverable quantities of lead and zinc and some contain a small amount of gold.

Open-File Report↗
USGS1981

Geologic, hydrologic, and chemical data from test wells in the Dickson area, Tennessee

Seventeen test wells were drilled at 12 sites in south central Dickson County, Tenn. Most of the sites were selected on the basis of carefully developed concepts of groundwater occurrence. These wells range from 20 to 400 feet deep and average 276 feet deep. The yields range from 0 to 300 gal/min and average 69 gal/min, with 6 wells yielding more than 100 gal/min. The water-bearing zones in rock that yield more than 50 gal/min are all between 100 and 200 feet below land surface. Sulfur gas was detected in two of the wells and large concentrations of iron were present in other wells. Capacity tests were conducted on those wells which yield more than 100 gal/min. The specific capacities of these wells range from 1.36 to 8.11 and average 3.46 gal/min for each foot of drawdown.

Tennessee↗
USGS2004

Studies by the U.S. Geological Survey on sources, transport, and fate of agricultural chemicals

The U.S. Geological Survey's National Water-Quality Assessment (NAWQA) Program is assessing the sources, transport, and fate of chemicals applied to crops in agricultural basins across the Nation (referred to as "study units," see map). Chemicals selected for study include nutrients (nitrogen and phosphorus) and about 50 commonly used pesticides and their transformation products, including triazine and acetanilide herbicides such as atrazine and metolachlor, and organophosphorus insecticides such as chlorpyrifos and diazinon. The basins in the studies represent a range of agricultural settings—with varying crop types and agricultural practices related to tillage, irrigation, artificial drainage, and chemical use—as well as a range of landscapes with different geology, soils, topography, climate, and hydrology. Consistent methodology and analysis allow comparisons among the different basins. This study design leads to an improved understanding of the many factors that can affect the movement of water and chemicals in different agricultural settings (see "Complex factors," next page). Information from these studies will help with decision-making related to chemical use, conservation, and other farming practices that are used to reduce runoff of agricultural chemicals and sediment from fields. This information also will benefit the U.S. Environmental Protection Agency, the Department of Agriculture, local and regional water managers, and agricultural chemical manufacturers who are involved in managing chemical use and pesticide registration.

Fact Sheet↗
USGS1976

Guidelines for sample collecting and analytical methods used in the U.S. Geological Survey for determining chemical composition of coal

This report is intended to meet the many requests for information on current U.S. Geological Survey procedures in handling coal samples. In general, the exact type and number of samples of coal and associated rock to be collected are left to the best judgment of the geologist. Samples should be of unweathered coal or rock and representative of the bed or beds sampled; it is recommended that two channel samples, separated by 10 to 100 yards (10 to 100 metres) and weighing 4 to 5 pounds ( 1.8 to 2.3 kilograms) each, be collected of each 5 feet ( 1.5 metres) of vertical section. Care must be taken to avoid any sample contamination, and to record the exact locality, thickness, and stratigraphic information for each sample. Analytical methods are described for the determination of major, minor, and trace elements in coal. Hg, As, Sb, F, Se, U, and Th are determined in the raw coal, and the following 34 elements are determined after ashing the coal: Si, Al, Ca, Mg, Na, K, Fe (total), Cl, Ti, Mn, P, S (total), Cd, Li, Cu, Zn, Pb, B, Ba, Be, Co, Cr, Ga, La, Mo, Nb, Ni, Sc, Sr, Ti, V, Y, Yb, and Zr. The methods used to determine these elements include atomic absorption spectroscopy, X-ray fluorescence spectroscopy, optical emission spectroscopy, spectrophotometry, selective-ion electrode, and neutron activation analysis. A split of representative coal samples is submitted to the U.S. Bureau of Mines for proximate, ultimate, forms of sulfur, and Btu determinations.

Circular↗
USGS2025

Applying geological unit distribution and chemical weathering indices to evaluate potential lithological sources of Al, As and Pb to the San Juan River, Four Corners region, USA

In arid to semi-arid landscapes, sporadic monsoonal events, varying widely in scale and distribution, can generate overland flow resulting in streamflow in ephemeral channels. These channels may contain metal-laden sediments that are a by-product of the weathering and erosion of local geological units. To evaluate the potential for local geology to contribute aluminium (Al), arsenic (As) and lead (Pb) to the San Juan River, northwestern New Mexico, USA, the distributions of geological units were delineated for 12 hydrological basins within the greater San Juan River watershed. Concentrations of Al, As and Pb in the predominant geological units were compiled from data in the National Geochemical Database. Chemical indices of weathering (CIW) were calculated for geological units with greater than 5% coverage in the entire San Juan River watershed. Based on CIWs of the major geological units, the Mesaverde Group (CIW = 95.2), Chinle and Dolores Formations ( combined ) (CIW = 93.3), and Mancos Shale ( combined ) (CIW = 82.6) are the most likely units to weather, erode and contribute sediments with elevated concentrations of Al, As and Pb to the San Juan River. The results of this study show the importance of understanding geological sources of sediments because they could be substantial contributors of constituents of concern to water, especially in arid environments where surface water may be the only source of water in the region.

Arizona, Colorado, New Mexico, Utah↗
USGS1984

The occurrence and behavior of radium in saline formation water of the U.S. Gulf Coast region

Radium has been measured in deep saline formation waters produced from a variety of U.S. Gulf Coast subsurface environments, including oil reservoirs, gas reservoirs and water-producing geopressured aquifers. A strong positive correlation has been found between formation-water salinity and Ra activity, resulting from the interaction of formation water with aquifer matrix. Ra isotopes enter the fluid phase after being produced by the decay of parent elements U and Th, which are located at sites on and within the solid matrix. Processes that are belived to be primarily responsible for transferring Ra from matrix to formation water are chemical leaching and alpha-particle recoil. Factors controlling the observed salinity-Ra relationship may be one or a combination of the following factors: (a) ion exchange; (b) increased solubility of matrix silica surrounding Ra atoms, coupled with a salinity-controlled rate of reequilibration of silica between solution and quartz grains; and (c) the equilibration of Ra in solution with detrial barite within the aquifer. No difference was found in the brine-Ra relation in water produced from oil or gas wells and water produced from wells penetrating only water-bearing aquifers, although the relation was more highly correlated for water-bearing aquifers than hydrocarbon-containing reservoirs. ?? 1984.

Chemical Geology↗
USGS2012

Distribution and geochemistry of selected trace elements in the Sacramento River near Keswick Reservoir

The effect of heavy metals from the Iron Mountain Mines (IMM) Superfund site on the upper Sacramento River is examined using data from water and bed sediment samples collected during 1996-97. Relative to surrounding waters, aluminum, cadmium, cobalt, copper, iron, lead, manganese, thallium, zinc and the rare-earth elements (REE) were all present in high concentrations in effluent from Spring Creek Reservoir (SCR), which enters into the Sacramento River in the Spring Creek Arm of Keswick Reservoir. SCR was constructed in part to regulate the flow of acidic, metal-rich waters draining the IMM Superfund site. Although virtually all of these metals exist in SCR in the dissolved form, upon entering Keswick Reservoir they at least partially converted via precipitation and/or adsorption to the particulate phase. In spite of this, few of the metals settled out; instead the vast majority was transported colloidally down the Sacramento River at least to Bend Bridge, 67 km from Keswick Dam. The geochemical influence of IMM on the upper Sacramento River was variable, chiefly dependent on the flow of Spring Creek. Although the average flow of the Sacramento River at Keswick Dam is 250 m 3 /s (cubic meters per second), even flows as low as 0.3 m 3 /s from Spring Creek were sufficient to account for more than 15% of the metals loading at Bend Bridge, and these proportions increased with increasing Spring Creek flow. The dissolved proportion of the total bioavailable load was dependent on the element but steadily decreased for all metals, from near 100% in Spring Creek to values (for some elements) of less than 1% at Bend Bridge; failure to account for the suspended sediment load in assessments of the effect of metals transport in the Sacramento River can result in estimates which are low by as much as a factor of 100.

California↗
USGS2014

Vibrational, X-ray absorption, and Mössbauer spectra of sulfate minerals from the weathered massive sulfide deposit at Iron Mountain, California

The Iron Mountain Mine Superfund site in California is a prime example of an acid mine drainage (AMD) system with well developed assemblages of sulfate minerals typical for such settings. Here we present and discuss the vibrational (infrared), X-ray absorption, and Mössbauer spectra of a number of these phases, augmented by spectra of a few synthetic sulfates related to the AMD phases. The minerals and related phases studied in this work are (in order of increasing Fe 2 O 3 /FeO): szomolnokite, rozenite, siderotil, halotrichite, römerite, voltaite, copiapite, monoclinic Fe 2 (SO 4 ) 3 , Fe 2 (SO 4 ) 3 ·5H 2 O, kornelite, coquimbite, Fe(SO 4 )(OH), jarosite and rhomboclase. Fourier transform infrared spectra in the region 750–4000 cm −1 are presented for all studied phases. Position of the FTIR bands is discussed in terms of the vibrations of sulfate ions, hydroxyl groups, and water molecules. Sulfur K-edge X-ray absorption near-edge structure (XANES) spectra were collected for selected samples. The feature of greatest interest is a series of weak pre-edge peaks whose position is determined by the number of bridging oxygen atoms between Fe 3+ octahedra and sulfate tetrahedra. Mössbauer spectra of selected samples were obtained at room temperature and 80 K for ferric minerals jarosite and rhomboclase and mixed ferric–ferrous minerals römerite, voltaite, and copiapite. Values of Fe 2+ /[Fe 2+ + Fe 3+ ] determined by Mössbauer spectroscopy agree well with those determined by wet chemical analysis. The data presented here can be used as standards in spectroscopic work where spectra of well-characterized compounds are required to identify complex mixtures of minerals and related phases.

California↗
USGS1979

Geology, coal resources, and chemical analyses of coal from the Fruitland Formation, Kimbeto EMRIA study site, San Juan County, New Mexico

The Kimbeto EMRIA study site, an area of about 20 square miles (52 km2), is located on the south margin of the San Juan Basin on the gently northward-dipping strata of the Upper Cretaceous Fruitland Formation and the Kirtland Shale. The coal beds are mainly in the lower 150 feet (45 m) of the Fruitland Formation. Coal resources--measured, indicated, and inferred--with less than 400 feet (120 m) of overburden in the site are 69,085,000 short tons (62,660,100 metric tons), 369,078,000 short tons (334,754,000 metric tons), and 177,803,000 short tons (161,267,000 metric tons) respectively. About 68 percent of these resources are overlain by 200 feet (60 m) or less of overburden. The apparent rank of the coal ranges from subbituminous B to subbituminous A. The average Btu/lb value of 14 core samples from the site on the as-received basis is 8,240 (4580 Kcal/kg), average ash content is 23.4 percent, and average sulfur content is 0.5 percent. Analyses of coal from the Kimbeto EMRIA study site show significantly higher ash content and significantly lower contents of volatile matter, fixed carbon, carbon, and a significantly lower heat of combustion when compared with other coal analyses from the Rocky Mountain province.

New Mexico↗