USGS Science⌕ Search

SEARCH · USGS Science

Results for “Chemical Geology”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 451 records · Page 25Linked to original sources

Water analyses from the laboratory of the United States Geological Survey

This paper contains 203 water analyses, which were made in the chemical laboratory of the United States Geological Survey. Most of these analyses have been published elsewhere, but many of the original documents are out of print, and are therefore obtainable with difficulty. Furthermore, the form of statement given the analyses has varied from time to time, so that the printed records show a lack of uniformity.

Water Supply Paper↗

Chapter G: Tentative Correlation Between CIPW Normin pl (Total Plagioclase) and Los Angeles Wear in Precambrian Midcontinental Granites-Examples from Missouri and Oklahoma, with Applications and Limitations for Use

The normative chemical classification of Cross, Iddings, Pirsson, and Washington (CIPW) is commonly used in igneous petrology to distinguish igneous rocks by comparing their magmatic chemistries for similar and dissimilar components. A potential use for this classification other than in petrologic studies is in the rapid assessment of aggregate sources, possibly leading to an economic advantage for an aggregate producer or user, by providing the opportunity to determine whether further physical testing of an aggregate is warranted before its use in asphalt or concrete pavement. However, the CIPW classification currently should not be substituted for the physical testing required in specifications by State departments of transportation. Demands for physical testing of aggregates have increased nationally as users seek to maximize the quality of the aggregate they purchase for their pavements. Concrete pavements are being laid with increased thicknesses to withstand increasing highway loads. New pavement mixes, most notably Superior Performance Asphalt Pavement ('Superpave'), are designed for additional service life. For both concrete and asphalt, the intent is to generate a durable pavement with a longer service life that should decrease overall life-cycle costs. Numerous aggregate producers possess chemical-composition data available for examination to answer questions from the potential user. State geological surveys also possess chemical-composition data for stone sources. Paired with the results of physical testing, chemical- composition data provide indicative information about stone durability and aggregate strength. The Missouri Department of Transportation has noted a possible relation among coarse-grained Precambrian granites of the midcontinental region, correlating the results of abrasion testing with the contents of normative minerals, also known as normins, calculated from chemical composition data. Thus, normin pl ( total plagioclase) can predict, by way of simple regression, the Los Angeles wear for granite samples collected in Missouri. The results of this abrasion testing were extended to another granite in Oklahoma where normin pl predicted Los Angeles wear to within 0.6 percent. This relation may also exist for granitic rocks outside the Oklahoma-Missouri region, as well as for other igneous-rock types.

Bulletin↗

Surface-water-quality assessment of the Upper Illinois River basin in Illinois, Indiana, and Wisconsin : data on manmade nonagricultural volatile and semivolatile organic chemicals in water, May 1988 through March 1990

This report contains data from the survey of manmade nonagricultural volatile and semivolatile organic chemicals in surface water in the upper Illinois River basin from May 1988 through March l990. In addition to the data, sampling methods and quality-assurance procedures are described. The survey was part of the upper Illinois River basin pilot project of the National Water-Quality Assessment program conducted by the U.S. Geological Survey. The organic chemicals analyzed from the water samples were those expected to be associated primarily with effluent from point sources in urban areas. A low-flow synoptic investigation of 52 volatile and 54 semivolatile organic chemicals was conducted at 31 sites in July 1988. Additional samples were collected monthly at two sites to continue to test for the presence of 43 volatile organic chemicals from December 1988 through March l990, and of all semivolatile organic chemicals at two sites from August through September 1988.

Open-File Report↗

Hydrologic data from an area southwest of Tallahassee, Florida, where municipal wastewater effluent is applied by spray irrigation

The effects of spray irrigation using municipal wastewater effluent on a ground-water system (in particular, on the water of the Floridan aquifer) were investigated. The area irrigated was 4 miles southwest of Tallahassee, Florida, on an area covered in part by pine forest and in part by selected grasses and forage crops. Hydrologic and geologic data were collected from 1972 to 1981. Hydrologic data include ground-water levels, water quality, and spray-irrigation rates. Ground-water level measurements were made at 60 wells. Water-quality samples were collected at 1 municipal wastewater effluent site, 3 springs, 17 soil sites, and 64 wells. Water-quality data were obtained from physical, chemical, and bacteriological analyses. Geologic data include geophysical logs and lithologic descriptions of 34 wells. (USGS)

Open-File Report↗

Chemical analyses of lignite from the Wilcox Group, Texas region, central and eastern Texas

As part of a continuing program by the U.S. Geological Survey to collect and chemically analyze representative sales of U.S. coal, 45 samples of lignite and lignite-associated rocks were collected strip mines and drill holes in Freestone and Milam counties in central Texas, and in Harrison, Rains, Titus, Van Zandt, and Wood Counties in eastern Texas. The sampled areas are in the Texas region of the Gulf province (Trumbull, 1960). Figure 1 shows the counties from which the samples were collected. Brief descriptions of the 45 samples are given in table 1. Thirty-one samples (twenty-six lignite and five lignite-associated rock) were collected from four active strip mines in Freestone, Harrison, Milam, and Titus Counties by the Texas Bureau of Economic Geology; 14 samples (13 lignite and 1 carbonaceous shale) were collected from nine drill holes in connection with the U.S. Bureau of Mines evaluation of coal resources in the proposed Carl L. Estes Lake site, Rains, Van Zandt, and Wood Counties (Ward, 1977). All samples included in this report are from the Wilcox Group of Eocene age. The Wilcox Group is undifferentiated in Harrison, Rains, Titus, Van Zandt, and Wood Counties. Lignite in this area is in the upper two-thirds of the Wilcox. In Freestone and Milam Counties, the Wilcox Group is subdivided into the Hooper, Simsboro, and Calvert Bluff Formations. Lignite in this area is predominantly in the Calvert Bluff Formation, with minor amounts in the Hooper Formation. A generalized stratigraphic column of the Wilcox Group and associated Tertiary strata is given in figure 2. The Calvert Bluff Formation and undifferentiated Wilcox Group consist of clastic debris deposited in a fluvial environment, in which major channel complexes characterized by sand deposition divide interchannel areas composed of mud. Lignite was deposited as a blanket peat in freshwater swamps and marshes within interchannel areas. Individual lignite beds are lenticular bodies extending 3 to 20 km laterally; thicknesses are generally 1 to 3 m, rarely as much as 6 m. Descriptions of geology and lignite occurrences are in Fisher (1963), Kaiser (1974, 1978), and Kaiser and others (1978).

Texas↗

Technical note—Relative variability of selected turbidity standards and sensors in use by the U.S. Geological Survey

The challenges associated with field measurements of turbidity are well known and result primarily from differences in reported values that depend on instrument design and the resulting need for reporting units that are specific to those designs. A critical challenge for making comparable turbidity measurements is the selection and use of appropriate turbidity standards for sensor calibration. The accepted primary standards for turbidity measurements use formazin made from scratch; all others should relate back to readings obtained using standard formazin. However, because turbidity is a qualitative property of water, comparing standards is not as simple as it is for many chemical measurements. The U.S. Geological Survey “National Field Manual for the Collection of Water-Quality Data” currently allows for the use of two standards, formazin and polymer beads, for the calibration of field turbidimeters. Another challenge for making comparable turbidity measurements is selection of turbidity sensors. A turbidity sensor commonly used in the U.S. Geological Survey, the Yellow Springs Instruments (YSI) 6136, has been replaced by the manufacturer with the YSI EXO turbidity sensor. Both sensors operate on the same principles but have slight design differences that result in readings that are not directly comparable on a 1:1 basis. Differences in calibration standards and sensors are a cause of concern in ongoing studies that require switching calibration standards or sensor types, and for comparisons of data collected with sensors calibrated by using different calibration standards, different sensor types, or both. The objectives of this study were to evaluate the response of two YSI turbidity sensors in both formazin-based standards (StablCal) and polymer turbidity standards (in this case YSI brand; however, other brands are available) and to compare the performance of the YSI EXO and YSI 6136 turbidity sensors under similar laboratory and environmental (field) conditions. To quantify these differences, a series of laboratory and field side-by-side comparisons were conducted. Nine field comparisons of YSI EXO and YSI 6136 sensors were performed at site locations in Kansas and Virginia. Two field comparisons of StablCal and polymer calibration standards were performed in Kansas, both using YSI EXO turbidity sensors. Five laboratory comparisons between the YSI EXO and YSI 6136 turbidity sensors were performed, and seven laboratory comparisons between StablCal and polymer turbidity standards were performed using YSI EXO turbidity sensors. The results can help the USGS and others better understand how turbidity data can differ depending on the sensors and calibration standards used. Key findings and conclusions include the following— Regardless of the comparison, strong linear associations were typically found across all measures of turbidity under field and laboratory conditions, but linear associations were not necessarily 1:1 and varied by type of standard, type of sensor, and field and laboratory conditions. The mean relative percentage differences for all but a few comparisons were greater than 10 percent but less than 30 percent. However, differences were inconsistent across the laboratory and field conditions measured in this study, precluding the ability to formulate definitive statements of consistent directional bias depending on the type of standard or sensor used. Across all tests and a range of 0 to 1,000 formazin nephelometric units (FNU), no consistent bias between the YSI EXO and YSI 6136 turbidity sensors was observed, but either regression relations were near 1:1 or the YSI EXO turbidity readings were lower than those measured with the YSI 6136. Relative percentage differences typically exceeded the 10- and 30-percent benchmarks. However, most (about 95 percent) of the absolute differences between turbidity values measured with the YSI EXO and those measured with the YSI 6136 sensors were less than 20 FNU. In laboratory experiments, when turbidity was “constant,” the absolute difference between YSI EXO and YSI 6136-measured turbidity values ranged from near 0 FNU to nearly 400 FNU (over a range of 0 to 1,000 FNU). Substantial variability in turbidity measurements makes comparison between standards and sensor types challenging. Given the inherent variability in turbidity measurements and the lack of consistent bias between calibration standards or sensors, changing methods during an ongoing study would compromise the comparability of the data. The effect of changing methods ultimately depends on study objectives. If method changes are required, laboratory- and field-based comparisons across a range of conditions ideally would be conducted to determine whether site-specific biases can be identified.

Open-File Report↗

Arsenic in groundwater in the North Carolina Eastern slate belt (Esb): Nash and halifax counties, north carolina

Naturally occurring arsenic-contaminated groundwater is present within the Eastern Slate Belt (ESB) of North Carolina. Long-term, integrated geologic and geo-chemical investigations havedetermined the presence of arsenic by analyzing precipitates from first and second order streams under base flow conditions. When groundwater discharges into streams, arsenic and other metals are precipitated from solution, due to redox changes between the subsurface and surface environments. Analyses (As, base metals, Fe and Mn) were determined following chemical extraction ofnaturally occurring manganese-iron oxide-coatings, which had precipitated from solution onto stream-bed cobbles. Additionally, artificial redox fronts were produced by placing ceramic tilesin streambeds to collect and analyze oxide precipitates. Thermochemical plots from these data, as well as information from respective stream water measurements (pH and Eh), water sampling, and rock chemical analyses indicate mobile arsenic in predicted stability fields. Initial results show that naturally occurring arsenic-contaminated groundwater is present within the study area. However, the resulting oxidation and pre-cipitation within streams appreciably removes thiscontaminant from surface water solution.

North Carolina↗

An investigation of ground-water recharge by injection in the Palo Alto Baylands, California: Hydraulic and chemical interactions — Final report

The U.S. Geological Survey, in cooperation with the Santa Clara Valley Water District, has completed a study of ground-water recharge by injection in the Palo Alto baylands along San Francisco Bay, California. Selected wells within the Water District 's injection-extraction network were monitored to determine hydraulic and chemical interactions affecting well-field operation. The well field was installed to prevent and eliminate saline contamination in the local shallow aquifer system. The primary focus of this study is on factors that affect injection efficiency, specifically well and aquifer clogging. Mixing and break-through curves for major chemical constituents indicate ion exchange, adsorption, and dissolution reactions. Freshwater breakthrough was detected in water-level data, which reflected fluid-density change as well as head buildup. Dissolution of calcium carbonate caused by dilution of saline ground water probably accounts for an apparent increase in specific capacity possibly related to improved aquifer permeability. Adsorption evidently removed trace elements during passage of injected water through the aquifer. In terms of hydraulic and chemical compatibility, the well field is a viable system for ground-water recharge. Aquifer heterogeneity and operational constraints reduce the efficiency of the system. Efficiency may be maximized by careful attention to extraction distribution and quantity and to injection distribution, quantity, and water quality. (USGS)

California↗

Methods for geochemical analysis

The laboratories for analytical chemistry within the Geologic Division of the U.S. Geological Survey are administered by the Office of Mineral Resources. The laboratory analysts provide analytical support to those programs of the Geologic Division that require chemical information and conduct basic research in analytical and geochemical areas vital to the furtherance of Division program goals. Laboratories for research and geochemical analysis are maintained at the three major centers in Reston, Virginia, Denver, Colorado, and Menlo Park, California. The Division has an expertise in a broad spectrum of analytical techniques, and the analytical research is designed to advance the state of the art of existing techniques and to develop new methods of analysis in response to special problems in geochemical analysis. The geochemical research and analytical results are applied to the solution of fundamental geochemical problems relating to the origin of mineral deposits and fossil fuels, as well as to studies relating to the distribution of elements in varied geologic systems, the mechanisms by which they are transported, and their impact on the environment.

Bulletin↗

Chemical analyses of coal from the Mesa Verde Formation, Grand Mesa coal field, Delta and Mesa counties, Colorado

As part of a continuing program by the U.S. Geological Survey to collect and chemically analyze representative samples of U.S. coals, 45 coal samples were collected from the Upper Cretaceous Mesaverde Formation, Grand Mesa coal field, Delta and Mesa Counties, Colorado. These samples were collected from cores (30 samples, 11 locations), mines (11 face channel samples, 9 locations), and from drill cuttings (4 samples, 1 location). U.S. Geological Survey sample numbers, index map locations, coal thickness or depth interval sampled, and brief descriptions for the 45 samples are listed in table 1. Sampling locations are shown in figure 1. Geophysical logs for all samples summarized in this report can be found in Eager (1978,1979).

Colorado↗

Sidescan sonar imagery and surficial geologic interpretation of the sea floor off Branford, Connecticut

The U.S. Geological Survey (USGS), in cooperation with the National Oceanic and Atmospheric Administration (NOAA) and the Connecticut Department of Environmental Protection (CT DEP), Figure 1 - Map of Study Areahas produced detailed geologic maps of the sea floor in Long Island Sound, a major East Coast estuary surrounded by the most densely populated region of the United States. These studies have built upon cooperative research between the USGS and the State of Connecticut that was initiated in 1982. The current phase of this research program is directed toward studies of sea-floor sediment distribution, processes that control sediment distribution, nearshore environmental concerns, and the relation of benthic community structures to the sea-floor geology. Anthropogenic wastes, toxic chemicals, and changes in land-use patterns resulting from residential, commercial, and recreational development have stressed the environment of the Sound, causing degradation and potential loss of benthic habitats (Koppelman and others, 1976; Long Island Sound Study, 1994). Detailed maps of the sea floor are needed to help evaluate the extent of adverse impacts and to help wisely manage resources in the future. Therefore, in a continuing effort to better understand Long Island Sound, we are constructing and interpreting sidescan sonar mosaics (complete-coverage acoustic images of the sea floor) within specific areas of special interest (Poppe and Polloni, 1998). The mosaic presented herein, which was produced during survey H11043 by NOAA 's Atlantic Hydrographic Branch, covers approximately 41.1 km 2 of the sea floor in north-central Long Island Sound off Branford, Connecticut. Shell bed provides shelter for juvenille skate.The mosaic and its interpretation serve many purposes, including: (1) defining the geological variability of the sea floor, which is one of the primary controls of benthic habitat diversity; (2) improving our understanding of the processes that control the distribution and transport of bottom sediments and the distribution of benthic habitats and associated infaunal community structures; and (3) providing a detailed framework for future research, monitoring, and management activities. The sidescan sonar mosaic also serves as a base map for subsequent sedimentological, geochemical, and biological observations, because precise information on environmental setting is important for selection of sampling sites and for appropriate interpretation of point measurements.

Connecticut↗

Sensitivity of high-elevation streams in the Southern Blue Ridge Province to acidic deposition

The Southern Blue Ridge Province, which encompasses parts of northern Georgia, eastern Tennessee, and western North Carolina, has been predicted to be sensitive to impacts from acidic deposition, owing to the chemical composition of the bedrock geology and soils. This study confirms the predicted potential sensitivity, quantifies the level of total alkalinity and describes the chemical characteristics of 30 headwater streams of this area. Water chemistry was measured five times between April 1983 and June 1984 at first and third order reaches of each stream during baseflow conditions. Sensitivity based on total alkalinity and the Calcite Saturation Index indicates that the headwater streams of the Province are vulnerable to acidification. Total alkalinity and p11 were generally higher in third order reaches (mean, 72 ?eq/? and 6.7) than in first order reaches (64 ?eq/? and 6.4). Ionic concentrations were low, averaging 310 and 340 ?eq/? in first and third order reaches, respectively. A single sampling appears adequate for evaluating sensitivity based on total alkalinity, but large temporal variability requires multiple sampling for the detection of changes in pH and alkalinity over time. Monitoring of stream water should continue in order to detect any subtle effects of acidic deposition on these unique resource systems.

Journal of the American Water Resources Associatio↗

Chemical analyses of coal from the Dakota and Straight Cliffs formations, southwestern Utah region, Kane and Garfield counties, Utah

As part of a continuing program by the U.S. Geological Survey to collect and chemically analyze representative samples of U.S. coals, 26 coal samples were collected from the Cretaceous Dakota and Straight Cliffs Formations, Southwestern Utah Region, Kane and Garfield Counties, Utah. Seven samples are from four core holes in the Dakota Formation of the Kolob coal field; nine samples are from six core holes and one face channel in the Dakota Formation of the Alton coal field; and ten samples are from three core holes in the Straight Cliffs Formation of the Kaiparowits Plateau coal field. The location of the Southwestern Utah Region and the Kolob, Alton and Kaiparowits Plateau coal fields are shown in figure 1 and sample localities are shown in figure 2. Brief descriptions for all 26 samples are given in table 1.

Utah↗

Comparison of gas chromatography/mass spectrometry and immunoassay techniques on concentrations of atrazine in storm runoff

Gas chromatography/mass spectrometry (GC/MS) and enzyme-linked immunosorbent assay (ELISA) techniques were used to measure concentrations of dissolved atrazine in 149 surface-water samples. Samples were collected during May 1992–September 1993 near the mouth of the White River (Indiana) and in two small tributaries of the river. GC/MS was performed on a Hewlett-Packard 5971 A, with electron impact ionization and selected ion monitoring of filtered water samples extracted by C-18 solid phase extraction; ELISA was performed with a magnetic-particle-based assay with photometric analysis. ELISA results compared reasonably well to GC/MS measurements at concentrations below the Maximum Contaminant Level for drinking water set by the U.S. Environmental Protection Agency (3.0 μg/L), but a systematic negative bias was observed at higher concentrations. When higher concentration samples were diluted into the linear range of calibration, the relation improved. A slight positive bias was seen in all of the ELISA data compared to the GC/MS results, and the bias could be partially explained by correcting the ELISA data for cross reactivity with other triazine herbicides. The highest concentrations of atrazine were found during the first major runoff event after the atrazine was applied. Concentrations decreased throughout the rest of the sampling period even though large runoff events occurred during this time, indicating that most atrazine loading to surface waters in the study area occurs within a few weeks after application. Use of brand names is for identification purposes only and does not constitute endorsement by the U.S. Geological Survey, the Uniroyal Chemical Company, or Wichita State University.

Indiana↗

An evaluation of procedures used in computing chemical denudation rates

Computations of chemical denudation rates (that is, the average rate of lowering of the earth's crust by chemical processes) should be based only upon those components of dissolved loads of streams that are derived from chemical weathering of rocks and soils, even though identification of those components is difficult and imprecise. Past computations of chemical denudation rates exaggerated by 1.4 to 2.4 times the significance of this process because they were calculated from total dissolved loads. Identification of separate denudation and nondenudation components in a water analysis can be done most readily for streams in crystalline silicate rock terrane where commonly 25 to 55 percent of the dissolved solids are HCO 3 −1 , SO 4 −2 , Cl −1 , and NO 3 −1 that cannot be derived from the underlying rock; instead these ions are derived either directly from the atmosphere or from atmosphere-biosphere interactions. Most of the remaining solutes are derived from chemical weathering or rainfall, or both. Existing data are often insufficient to separate these two components, but atmospheric contributions to dissolved loads of dilute natural waters are substantial. The commonly observed increased concentration of dissolved solids in chemically polluted rivers is produced by concentration of natural dissolved loads by evaporation, and by addition of solutes not present in natural waters. Concentration of natural solutes represents a modification of natural denudation processes that does not change the rate of denudation. Addition of new solutes represents man-induced, accelerated chemical denudation. Extrapolation of modern chemical denudation rates to geologic situations is extremely imprecise because of uncertainties in assessing man's influence on present dissolved loads, in reconstructing the number and magnitude of past climatic changes, and in evaluating the effects of evolving flora and fauna.

Bulletin of the Geological Society of America↗

Origin of precambrian iron formations

A statistical study of the chemical composition of the Precambrian iron formations of the Canadian Shield affords a new approach to the origin of these unusual formations . The average total iron content of 2,200 samples from the literature and from unpublished mining company analyses is 26.7 percent Fe. The average Fe content for 16 iron formations in the United States and Canada ranges from 24.5 to 34.1 percent. Low contents of A1203, Ti02, P2O5, and CaO characterize the Precambrian iron formations compared to the relatively large amounts of these constituents in the post- Precambrian iron -bearing sediments. The chemical data emphasize that whereas iron , manganese, and silica were transported and deposited together in the cherty iron formations of the Precambrian , these same elements were chemically differentiated in younger geological time in large but separate deposits of iron and silica. Isotopic age determinations indicate that cherty iron formations were deposited during a long interval of geologic time from approximately 1,700 to 3,000 million years ago. A model is proposed to explain the origin of the iron formations of the Lake Superior type based on the absence or marked deficiency of free oxygen in the atmosphere prior to the Late Precambrian . Lateritic weathering under these conditions permitted the transport of iron and manganese together with silica. The weathered mantle effectively retained aluminum, titanium, phosphorus, and colloidal clay. Graphitic material of biogenic origin is closely associated with the Precambrian iron formations . Although it is uncertain whether iron was precipitated directly through biologic processes, the removal of C02 and the liberation of oxygen to the sea water through photosynthesis of primitive plants undoubtedly influenced the energy relationships among the iron minerals. As a result of the variable conditions the iron formations commonly are characterized by nonequilibrium mineral assemblages. In Late Precambrian time a critical level of free oxygen in the atmosphere was attained permitting a marked acceleration in plant growth and in accretion of oxygen. This stage in the development of an oxygenated atmosphere was reached at least 1,200 million years ago and effectively curtailed the development of cherty iron formations of the Lake Superior type.

Economic Geology↗

Crossing disciplines and scales to understand the critical zone

The Critical Zone (CZ) is the system of coupled chemical, biological, physical, and geological processes operating together to support life at the Earth's surface. While our understanding of this zone has increased over the last hundred years, further advance requires scientists to cross disciplines and scales to integrate understanding of processes in the CZ, ranging in scale from the mineral-water interface to the globe. Despite the extreme heterogeneities manifest in the CZ, patterns are observed at all scales. Explanations require the use of new computational and analytical tools, inventive interdisciplinary approaches, and growing networks of sites and people.

Elements↗

Biosolids, Crop, and Ground-Water Data for a Biosolids-Application Area Near Deer Trail, Colorado, 2004 Through 2006

From 2004 through 2006, the U.S. Geological Survey monitored the chemical composition of biosolids, crops, dust, and ground water related to biosolids applications near Deer Trail, Colorado, in cooperation with the Metro Wastewater Reclamation District. This monitoring effort was a continuation of the monitoring program begun in 1999 in cooperation with the Metro Wastewater Reclamation District and the North Kiowa Bijou Groundwater Management District. The monitoring program addresses concerns from the public about the chemical effects from applications of biosolids to farmland in the Deer Trail, Colorado, area. This report presents chemical data from 2004 through 2006 for biosolids, crops, and alluvial and bedrock ground water. The chemical data include the constituents of highest concern to the public (arsenic, cadmium, copper, lead, mercury, molybdenum, nickel, selenium, zinc, and plutonium) in addition to many other constituents. The ground-water section also includes climate and water-level data.

Data Series↗