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 1,315 records · Page 73Linked to original sources

Thermal springs in Lake Baikal

Pore waters extracted from sediment cores were analyzed for their oxygen and hydrogen isotopic compositions and major ion chemistry to determine the source of water from a vent area for diffuse lake-bottom thermal springs or seeps in Frolikha Bay, northeastern Lake Baikal. The δ 18 O values of pore waters range from -15.2‰ to -16.7‰, and δD values range from -119‰ to -126‰ (both isotopes determined relative to standard mean ocean water [SMOW]). Bottom water in Lake Baikal has a δ 18 O value of -5.6‰ and a δD value of -120‰ Pore waters in the vent area are significantly enriched in Mg, B, Ca, and especially Na and have the lowest δD and δ 18 O values; these pore waters are isotopically and chemically distinct from pore waters in other, more typical parts of the lake. The pore-water isotopic data fall on a local meteoric water line, and covariations in water isotopes and chemistry are not consistent with evaporation or hydrothermal water-rock interaction. The thermal springs represent discharging meteoric waters that have been gently heated during subsurface circulation and are largely unaltered isotopically. Chemical variations are most likely due to dissolution of subsurface evaporites.

Geology↗

A method for discriminating between biogenic and chemical origins of the ore-stage pyrite in a roll-type uranium deposit

Some roll-type uranium deposits are marginal to an altered tongue in sandstone beds that originally contained more-or-less uniformly distributed pyrite. Mineralizing solutions percolated through the sandstone, oxidized nearly all the pre-existing pyrite, and then redeposited part of the pyrite downstream in an embryonic ore zone. The pyrite and the entire ore zone continued to migrate downstream in the sandstone, much as a sand dune migrates. The amount of pyrite in mature deposits varies systematically with the position in the ore body. It is postulated that the rate at which the pyrite was redeposited controlled the systematic variation in distribution of pyrite.Biogenic and chemical models which are described in the literature provide alternate explanations for the genesis of roll-type uranium deposits in sandstone. The different theoretical rates for the precipitation of pyrite in the two genetic models provide a distinctive distribution of pyrite that characterizes each process. The theoretical difference between the biogenic and chemical models provides a mathematical technique for identifying the origin of a deposit. Mathematical analysis of the pyrite content of a uranium deposit in the Shirley Basin, Wyoming, illustrates a practical application of the theory. Although a definite conclusion about the origin of roll-type deposits would require considerably more data than are now available, the pyrite content of this deposit does correspond to the theoretical pyrite content of the chemical model, suggesting that a disproportionation reaction was involved in its formation.

Wyoming↗

Atrazine concentrations in near-surface aquifers: A censored regression approach

In 1991, the U.S. Geological Survey (USGS) conducted a study to investigate the occurrence of atrazine (2-chloro-4-ethylamino-6- isopropylamino-s-triazine) and other agricultural chemicals in near-surface aquifers in the midcontinental USA. Because about 83% of the atrazine concentrations from the USGS study were censored, standard statistical estimation procedures could not be used. To determine factors that affect atrazine concentrations in groundwater while accommodating the high degree of data censoring. Tobit models were used (normal homoscedastic, normal heteroscedastic, lognormal homoscedastic, and lognormal heteroscedastic). Empirical results suggest that the lognormal heteroscedastic Tobit model is the model of choice for this type of study. This model determined the following factors to have the strongest effect on atrazine concentrations in groundwater: percent of pasture within 3.2 km, percent of forest within 3.2 km (2 mi), mean open interval of the well, primary water use of a well, aquifer class (unconsolidated or bedrock), aquifer type (unconfined or confined), existence of a stream within 30 m (100 ft), existence of a stream within 30 m to 0.4 km (0.25 mi), and existence of a stream within 0.4 to 3.2 km. Examining the elasticities of the continuous explanatory factors provides further insight into their effects on atrazine concentrations in groundwater. This study documents a viable statistical method that can be used to accommodate the complicating presence of censured data, a feature that commonly occurs in environmental data.

Journal of Environmental Quality↗

Methods of collection and quality assessment of arsenic data in well-water supplies in Maine, 2001–2 and 2006–7

The U.S. Geological Survey, in cooperation with the U.S. Centers for Disease Control and Prevention and the Maine Center for Disease Control and Prevention, assessed the chemical characteristics and the occurrence, distribution, and oxidation state of inorganic arsenic in drinking water from selected domestic well-water supplies in Maine in 2001–2 and 2006–7. The data collected provide support for evaluating arsenic-removal efficiencies of household water-purification systems and provide information to State and local officials that can be used in determining a water-treatment approach for the removal of arsenic from drinking water.

Maine↗

Selected Physical, Chemical, and Biological Data Used to Study Urbanizing Streams in Nine Metropolitan Areas of the United States, 1999-2004

This report documents and summarizes physical, chemical, and biological data collected during 1999-2004 in a study titled Effects of Urbanization on Stream Ecosystems, undertaken as part of the U.S. Geological Survey's National Water-Quality Assessment Program. Data-collection methods and data processing are described in this report for streamflow; stream temperature; instream chemistry; instream aquatic habitat; and algal, macroinvertebrate, and fish communities. Data summaries prepared for analytical use are presented in downloadable data tables.

Data Series↗

Brianna postcard

Brianna is a hydrologist in the Hydrologic Investigations (Studies) Unit. She received a bachelor of science degree in chemical engineering and a master’s degree in civil engineering from the University of Kansas.

General Information Product↗

Pesticides data-collection activities of the U.S. Geological Survey in Texas

The water-resources investigations program of the Geological Survey has the objective of seeing that the Nation's water resources are appraised and that the necessary water data to develop and manage them efficiently are available when needed. In carrying out this objective, the Survey is the primary source of hydrologic data that are basic not only to the quantification of the water resource but also to its development and conservation. In recent years, the need has developed for the Survey to provide data and technology to predict the impact of man's activities upon the water resource and the water environment. To accomplish its mission, the Geological Survey determines the source, quantity, quality, distribution, movement, and availability of both surface and ground water. This work includes the assessment of the chemical, physical, and biological quality of water resources and its relation to various parts of the hydrologic cycle; research to improve the scientific basis of investigations and techniques; design and operation of a national water-data network; and publication of its investigations.

Texas↗

Characterization and modes of occurrence of elements in feed coal and coal combustion products from a power plant utilizing low-sulfur coal from the Powder River Basin, Wyoming

The U.S. Geological Survey and the University of Kentucky Center for Applied Energy Research are collaborating with an Indiana utility company to determine the physical and chemical properties of feed coal and coal combustion products from a coal-fired power plant. The Indiana power plant utilizes a low-sulfur (0.23 to 0.47 weight percent S) and lowash (4.9 to 6.3 weight percent ash) subbituminous coal from the Wyodak-Anderson coal zone in the Tongue River Member of the Paleocene Fort Union Formation, Powder River Basin, Wyoming. Based on scanning electron microscope and X-ray diffraction analyses of feed coal samples, two mineral suites were identified: (1) a primary or detrital suite consisting of quartz (including beta-form grains), biotite, feldspar, and minor zircon; and (2) a secondary authigenic mineral suite containing alumino-phosphates (crandallite and gorceixite), kaolinite, carbonates (calcite and dolomite), quartz, anatase, barite, and pyrite. The primary mineral suite is interpreted, in part, to be of volcanic origin, whereas the authigenic mineral suite is interpreted, in part, to be the result of the alteration of the volcanic minerals. The mineral suites have contributed to the higher amounts of barium, calcium, magnesium, phosphorus, sodium, strontium, and titanium in the Powder River Basin feed coals in comparison to eastern coals. X-ray diffraction analysis indicates that (1) fly ash is mostly aluminate glass, perovskite, lime, gehlenite, quartz, and phosphates with minor amounts of periclase, anhydrite, hematite, and spinel group minerals; and (2) bottom ash is predominantly quartz, plagioclase (albite and anorthite), pyroxene (augite and fassaite), rhodonite, and akermanite, and spinel group minerals. Microprobe and scanning electron microscope analyses of fly ash samples revealed quartz, zircon, and monazite, euhedral laths of corundum with merrillite, hematite, dendritic spinels/ferrites, wollastonite, and periclase. The abundant calcium and magnesium mineral phases in the fly ash are attributed to the presence of carbonate, clay, and phosphate minerals in the feed coal and their alteration to new phases during combustion. The amorphous diffraction-scattering maxima or glass 'hump' appears to reflect differences in chemical composition of fly ash and bottom ash glasses. In Wyodak-Anderson fly and bottom ashes, the center point of scattering maxima is due to calcium and magnesium content, whereas the glass 'hump' of eastern fly ash reflects variation in aluminum content. The calcium- and magnesium-rich and alumino-phosphate mineral phases in the coal combustion products can be attributed to volcanic minerals deposited in peat-forming mires. Dissolution and alteration of these detrital volcanic minerals occurred either in the peat-forming stage or during coalification and diagenesis, resulting in the authigenic mineral suite. The presence of free lime (CaO) in fly ash produced from Wyodak-Anderson coal acts as a self-contained 'scrubber' for SO3, where CaO + SO3 form anhydrite either during combustion or in the upper parts of the boiler. Considering the high lime content in the fly ash and the resulting hydration reactions after its contact with water, there is little evidence that major amounts of leachable metals are mobilized in the disposal or utilization of this fly ash.

Scientific Investigations Report↗

Water Resources Data - Wisconsin, Water Year 2002

Water-resources data for the 2002 water year for Wisconsin include records of streamflow at gaging stations, partial record stations, and miscellaneous sites, records of precipitation, and records of chemical, biological, and physical characteristics of surface water. In addition, water levels in observation wells are reported. These data were collected by the U.S. Geological Survey in cooperation with State and local agencies and other Federal agencies in Wisconsin.

Water Data Report↗

Water Resources Data - Wisconsin, Water Year 2003

Water-resources data for the 2003 water year for Wisconsin include records of streamflow at gaging stations, partialrecord stations, and miscellaneous sites, records of precipitation, and records of chemical, biological, and physical characteristics of surface water. In addition, water levels in observation wells are reported. These data were collected by the U.S. Geological Survey in cooperation with State and local agencies and other Federal agencies in Wisconsin.

Water Data Report↗

Water resources data - Wisconsin, water year 2005

Water-resources data for the 2005 water year for Wisconsin include records of streamflow at gaging stations, partial-record stations, and miscellaneous sites, records of precipitation, and records of chemical, biological, and physical characteristics of surface water. In addition, water levels in observation wells are reported. These data were collected by the U.S. Geological Survey in cooperation with State and local agencies and other Federal agencies in Wisconsin.

Water Data Report↗

Mineralogical studies of the nitrate deposits of Chile IV. Brüggenite, Ca(IO3)2-H2O, a new saline mineral

Br ü ggenite, Ca(I0 3 )2 - H2 0, is found in veins of high-purity soda niter in rhyolite tuff at Pampa Pique III, Oficina Lautaro, Chile, as long columnar anhedral crystals, as prismatic crystals, and as irregular anhedral crystals or encrusting masses. The mineral is colorless to bright yellow, and transparent to translucent, has vitreous luster and a hardness of about 3 1 / 2 , is brittle, and has conchoidal fracture. It is biaxial and has variable optic angle and refractive indices, which were determined by the spindle-stage method. Refractive indices are as follows: n α =1.772-1.779, n β =1.795-1.802, and n γ =1.817-1.824 (all ± 0.003); optic angle shows a range of 2 V Z = 86°-96°; Z = b and X ∧ c = -47°; dispersion (Z) is r < v , moderate. Brüggenite is monoclinic, space group P 2 1 / c , with a=8.509±0.001 A, b = 10.027±0.002 A, c = 7.512±0.001 A, β = 95°16.00'±0.55', volume 638.2 A 3 , Z = 4, G (calc) = 4.244, G (meas) =4.24±0.01. The X-ray diffraction powder pattern of brüggenite has the following strong lines ( hkl , d hkl 1 ): 031, 3.051 A (100); 220, 3.238 A (90); 200, 4.235 A (80); 002, 3.739 A (60); 012, 3.503 A (60); 231, 2.522 A (60). The composition was confirmed by chemical analyses.

Antofagasta Province↗

Hydrogeology, chemical characteristics, and water sources and pathways in the zone of contribution of a public-supply well in San Antonio, Texas

In 2001, the National Water-Quality Assessment (NAWQA) Program of the U.S. Geological Survey initiated a series of studies on the transport of anthropogenic and natural contaminants (TANC) to public-supply wells (PSWs). The main goal of the TANC project was to better understand the source, transport, and receptor factors that control contaminant movement to PSWs in representative aquifers of the United States. Regional- and local-scale study areas were selected from within existing NAWQA study units, including the south-central Texas Edwards aquifer. The local-scale TANC study area, nested within the regional-scale NAWQA study area, is representative of the regional Edwards aquifer. The PSW selected for study is within a well field of six production wells. Although a single PSW was initially selected, because of constraints of well-field operation, samples were collected from different wells within the well field for different components of the study. Data collected from all of the well-field wells were considered comparable because of similar well construction, hydrogeology, and geochemistry. An additional 38 PSWs (mostly completed in the confined part of the aquifer) were sampled throughout the regional aquifer to characterize water quality. Two monitoring well clusters, with wells completed at different depths, were installed to the east and west of the well field (the Zarzamora and Timberhill monitoring well clusters, respectively). One of the monitoring wells was completed in the overburden to evaluate potential hydrologic connectivity with the Edwards aquifer. Geophysical and flowmeter logs were collected from one of the well-field PSWs to determine zones of contribution to the wellbore. These contributing zones, associated with different hydrogeologic units, were used to select monitoring well completion depths and groundwater sample collection depths for depth-dependent sampling. Depth-dependent samples were collected from the PSW from three different depths and under three different pumping conditions. Additionally, selected monitoring wells and one of the well-field PSWs were sampled several times in response to a rainfall and recharge event to assess short-term (event-scale) temporal variations in water quality. For comparison purposes, groundwater samples were categorized as being from regional aquifer PSWs, from the well field (wellhead samples), from the monitoring wells (excluding the overburden well), from the overburden well, from the PSW depth-dependent sampling, and from temporal sampling. Groundwater samples were analyzed for inorganic, organic, isotopic, and age-dating tracers to characterize geochemical conditions in the aquifer and provide understanding of the mechanisms of mobilization and movement of selected constituents from source areas to a PSW. Sources, tracers, and conditions used to assess water quality and processes affecting the PSW and the aquifer system included (1) carbonate host rock composition; (2) physicochemical constituents; (3) major and trace element concentrations; (4) saturation indices with respect to minerals in aquifer rocks; (5) elemental ratios, such as magnesium to calcium ratios, that are indicative of water-rock interaction processes; (6) oxidation-reduction conditions; (7) nutrient concentrations, in particular nitrate concentrations; (8) the isotopic composition of nitrate, which can point to specific nitrate sources; (9) strontium isotopes; (10) stable isotopes of hydrogen and oxygen; (11) organic contaminant concentrations, including pesticides and volatile organic compounds; (12) age tracers, apparent-age distribution, and dissolved gas data used in age interpretations; (13) depth-dependent water chemistry collected from the PSW under different pumping conditions to assess zones of contribution; and (14) temporal variability in groundwater composition from the PSW and selected monitoring wells in response to an aquifer recharge event. Geochemical results indicate that the well-field and monitoring well samples were largely representative of groundwater in the regional confined aquifer. Constituents of concern in the Edwards aquifer for the long-term sustainability of the groundwater resource include the nutrient nitrate and anthropogenic organic contaminants. Nitrate concentrations (as nitrogen) for regional aquifer PSWs had a median value of 1.9 milligrams per liter, which is similar to previously reported values for the regional aquifer. Nitrate-isotope compositions for groundwater samples collected from the well-field PSWs and monitoring wells had a narrow range, with values indicative of natural soil organic values. A comparison with historical nitrate-isotope values, however, suggests that a component of nitrate in groundwater from biogenic sources might have increased over the last 30 years. Several organic contaminants (the pesticide atrazine, its degradate deethylatrazine, trichloromethane (chloroform; a drinking-water disinfection byproduct), and the solvent tetrachloroethene (PCE)) were widely distributed throughout the regional aquifer and in the local-scale TANC study area at low concentrations (less than 1 microgram per liter). Higher concentrations of PCE were detected in samples from the well-field PSWs and Zarzamora monitoring wells relative to the regional aquifer PSWs. The urban environment is a likely source of contaminants to the aquifer, and these results indicate that one or more local urban sources might be supplying PCE to the Zarzamora monitoring wells and the well-field wells. Samples from the well field also had high concentrations of chloroform relative to the monitoring wells and regional aquifer PSWs. For samples from the regional aquifer PSWs, the most frequently detected organic contaminants generally decreased in concentration with increasing well depth. Deeper wells might intercept longer regional flow paths with higher fractions of older water or water recharged in rural recharge areas in the western part of the aquifer that have been less affected by anthropogenic contaminants. A scenario of hypothetical contaminant loading was evaluated by using results from groundwater-flow-model particle tracking to assess the response of the aquifer to potential contamination. Results indicate that the aquifer responds quickly (less than 1 year to several years) to contaminant loading; however, it takes a relatively long time (decades) for concentrations to reach peak values. The aquifer also responds quickly (less than 1 year to several years) to the removal of contaminant loading; however, it also takes a relatively long time (decades) to reach near background concentrations. Interpretation of geochemical age tracers in this well-mixed karst system was complicated by contamination of a majority of measured tracers and complexities of extensive mixing. Age-tracer results generally indicated that groundwater samples were composed of young, recently recharged water with piston-flow model ages ranging from less than 1 to 41 years, with a median of 17 years. Although a piston-flow model is typically not valid for karst aquifers, the model ages provide a basis for comparing relative ages of different samples and a reference point for more complex hydrogeologic models for apparent-age interpretations. Young groundwater ages are consistent with particle-tracking results from hydrogeologic modeling for the local-scale TANC study area. Age-tracer results compared poorly with other geochemical indicators of groundwater residence time and anthropogenic effects on water quality, indicating that hydrogeologic conceptual models used in groundwater age interpretations might not adequately account for mixing in this karst system. Groundwater samples collected from the well field under a variety of pumping conditions were relatively homogeneous and well mixed for numerous geochemical constituents (with the notable exception of age tracers). Groundwater contributions to the PSW were dominated by well-mixed, relatively homogeneous groundwater, typical of the regional confined aquifer. Zones of preferential flow were determined for the PSW, but groundwater samples from different stratigraphic units were not geochemically distinct. Variations in chemical constituents in response to a rainfall and aquifer recharge event occurred but were relatively minor in the PSW and monitoring wells. This observation is consistent with the hypothesis that the response to individual recharge events in the confined aquifer, unless intersecting conduit flow paths, might be attenuated by mixing processes along regional flow paths. Results of this study are consistent with the existing conceptual understanding of aquifer processes in this karst system and are useful for water-resource development and management practices.

Texas↗

PFAS in the environment

The U.S. Geological Survey (USGS) is working with Federal, State, and local partners to monitor and evaluate perfluoroalkyl and polyfluoroalkyl substances (PFAS) in the State’s groundwater and surface waters. PFAS are synthetic chemicals with widespread commercial and industrial use that can take a very long time to break down in the environment and may affect human health. The USGS in New York is working with experts across the Nation to develop and implement rigorous and innovative techniques to detect PFAS at concentrations as low as parts per trillion to help the public understand the spatial distribution and magnitude of PFAS contamination within the environment.

General Information Product↗

Quaternary geologic map of the Regina 4° x 6° quadrangle, United States and Canada

For scientific purposes, the map differentiates Quaternary surficial deposits and materials on the basis of clast lithology or composition, matrix texture or particle size, structure, genesis, stratigraphic relations, engineering geologic properties, and relative age, as shown on the correlation diagram and indicated in the 'Description of Map Units'. Deposits of some constructional landforms, such as end moraines, are distinguished as map units. Deposits of erosional landforms, such as outwash terraces, are not distinguished, although glaciofluvial, ice-contact, fluvial, and lacustrine deposits that are mapped may be terraced. Differentiation of sequences of fluvial and glaciofluvial deposits at this scale is not possible. For practical purposes, the map is a surficial materials map. Materials are distinguished on the basis of lithology or composition, texture or particle size, and other physical, chemical, and engineering characteristics. It is not a map of soils that are recognized and classified in pedology or agronomy. Rather, it is a generalized map of soils as recognized in engineering geology, or of substrata or parent materials in which pedologic or agronomic soils are formed. As a materials map, it serves as a base from which a variety of maps for use in planning engineering, land-use planning, or land-management projects can be derived and from which a variety of maps relating to earth surface processes and Quaternary geologic history can be derived.

Regina quadrangle↗