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Results for “Chemical Geology”

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

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At least 811 records · Page 45Linked to original sources
USGS1980

Chemical and physical characteristics of natural ground waters in Michigan: A preliminary report

Wide variations occur in the chemical and physical characteristics of natural groundwaters in Michigan. Dissolved-solids concentrations range from 23 to 2,100 milligrams per liter. Waters having low dissolved-solids concentrations are calcium bicarbonate waters. Sodium, sulfate, and chloride increase as mineralization increases. Iron, aluminum, and titanium are higher at some locations than is common in most natural waters. Lead concentrations exceed those desirable in drinking water at some locations in the northern part of the Lower Peninsula. Generalized areal patterns of water quality variation suggest that geology is a primary cause of differences across the State. Examples of chemical associations in water suggest that chemical analyses may be valuable in tracing and identifying mineral deposits.

Michigan↗
USGS1989

Natural ground-water quality in Michigan, 1974-87

Wide variations occur in the chemical and physical characteristics of natural groundwaters in Michigan. Dissolved-solids concentrations range from 20 to 76,000 mg/L. Waters having low dissolved-solids concentrations are calcium bicarbonate-type waters. Sodium, sulfate, and chloride increase as mineralization increases. Iron, aluminum, and titanium concentrations are higher at some locations than is common in most natural waters. Lead concentrations exceed U.S. Environmental Protection Agency 's primary drinking-water regulations at some locations in the northern part of the lower Peninsula. Generalized areal patterns of water-quality variability indicate that geology is a primary cause of differences across the State. Examples of chemical associations in water indicate that chemical analyses may be valuable in tracing and identifying mineral deposits.

Michigan↗
USGS2007

Aquatic Communities and Selected Water Chemistry in St. Vrain Creek near the City of Longmont, Colorado, Wastewater-Treatment Plant, 2005 and 2006

In 2005, the U.S. Geological Survey and the City of Longmont, Colo., began a study to document chemical characteristics of St. Vrain Creek that had previously been unavailable either due to high cost of analysis or lack of analytical capability. Stream samples were collected at seven sites on St. Vrain Creek during the spring of 2005 and 2006 for analysis of wastewater compounds. A Lagrangian-sampling design was followed during each sampling event, and time-of-travel studies were conducted just prior to each sampling event to determine appropriate sampling times for the synoptic. In addition, semipermeable membrane devices, passive samplers that concentrate hydrophobic organic chemicals, were installed at six sites during the spring of 2005 and 2006 for approximately 4 weeks. After retrieval, contaminant residues concentrated in the semipermeable membrane devices were recovered and used in a toxicity assay that provided a screen for aryl hydrocarbon receptor type compounds, including polycyclic aromatic hydrocarbons, polychlorinated biphenyls, dioxins, and furans. In addition, the U.S. Geological Survey summarized information on macroinvertebrate and fish communities known from St. Vrain Creek dating back to the early 1900s in order to assess their utility in evaluating wastewater-treatment plant upgrades and habitat improvement projects. Unfortunately, because of inconsistencies in data collection these data cannot be used as intended; however, they are useful for understanding to some degree gross patterns in fish species distribution, but less so for macroinvertebrates.

Data Series↗
USGS2020

Fate and behavior tools related to inland spill response—Workshop on the U.S. Geological Survey’s role in Federal science support

Executive Summary There is a growing body of tools available for science support for determining the fate and behavior of industrial and agricultural chemicals that are rapidly injected (“spilled”) into aquatic environments. A 2-day roundtable-style workshop was held by the U.S. Geological Survey (USGS) in Middleton, Wisconsin, in December 2017 to describe and explore existing Federal science support for spill fate and behavior tools used for inland spills, ongoing and new fate and behavior studies, and science gaps in planning and response tools as part of the USGS Midcontinent Region’s efforts to include spill response as part of its strategic plans. A total of 28 attendees representing a variety of Federal, State, and regional entities presented on programs and tools used in various aspects of spill response. Most programs and tools discussed were for spills in riverine environments but tools and applications for spills in lakes, on land surfaces, in urban storm sewer networks, and groundwater also were discussed. A primary workshop focus was to facilitate communication and increase potential for future collaboration among agencies for inland spill science support. The role and need for more USGS science support within the inland spill community was discussed. Enhanced communication is needed within the USGS and the U.S. Department of the Interior science programs, as well as within and among other agencies that do emergency planning and response. A main conclusion of the workshop was that there are untapped resources of the USGS outlined in the agency’s science strategy that could strengthen science support for fate and behavior tools in inland areas, especially in the Upper Mississippi River, Ohio River, and Great Lakes Basins where large freshwater resources overlap with dense corridors of oil and hazardous substances, with transportation networks, and with large populations centers. Fate and behavior tools are being developed quickly for inland spill response by multiple Federal agencies in partnership with local and regional entities. Applicability of these tools ranges from planning and preparedness, to the early stages of spill response for protection of human life and property, and to the application of monitoring and models to assess the long-term consequences of spills. Key findings from the workshop, with an emphasis on potential further development of USGS science support, include the following: •The national and regional response to spills occurs within an established system that must be respected by all parties involved in spill response. The USGS’s role is to support spill responders who are physically working at a spill scene, deploying booms and using other efforts to contain and recover spilled materials. •The USGS has tools that have been used throughout spill response operations, from early response to recovery and restoration. Developing a more formal role for the USGS to participate in science support for inland spills on a consistent basis is a desired outcome. This will require the USGS to improve internal and external communication and would be best accomplished by assigning one or more coordinator positions within the agency to plan and oversee USGS spill-response efforts. More involvement of the USGS on National and Regional Response Teams, especially in the realm of the Science and Technology Subcommittees, will gofar in increasing external communication and integration of fate and behavior tools. •Rapid response to spills requires modeling and mapping of plumes and associated time-of-travel estimation for a range of stream sizes across the United States. Many existing models use USGS streamgage data and the USGS National Hydrography Dataset. Nearly all existing models would benefit from updated linkages to USGS StreamStats and its soon-to-be released time-of-travel estimates,real-time velocity, stream morphology, and slope data. Integrating USGS tools with those from other agencies could be done to better serve the larger spill response community. • A problem is that existing models to rapidly predict plume extent, as well as more followup/longer-term fate and transport models, can be unknown or unavailable to spill responders. Thus, creating and strengthening linkages among USGS scientists skilled at using these tools is needed to support spill response with the on-scene responders. • Research for inland spill fate and behavior done outside of an immediate spill response can assist with spill planning and preparedness by (1) revealing sites likely to experience spills in the future (high-risk sites) and (2) understanding how a spilled substance might behave under a range of environmental conditions. However, USGS research on this topic has been scarce and subject to funding availability. Examples include the 2010 Line 6B Spill release into the Kalamazoo River in Michigan, where the USGS provided science support for a variety of fate and behavior tools for stream and impoundment environments. A long-term research site in Bemidji, Minnesota, provides important insights into transformations and longevity of spilled oil in groundwater and groundwater-surface water interactions. • Linking stream models to other components of this inland environment, including groundwater, overland flow, and karst, is needed. Stream network data can be linked to underground conduits such as storm sewers and karst groundwater systems. Stream models can also be linked with geospatial data such as that contained in U.S. Environmental Protection Agency’s interactive mapping tools. • The USGS is uniquely qualified to collect water-quality data during spills in the United States because of its many geographically dispersed water science centers, its knowledge and preparedness for flood measurement and documentation, and its cadre of skilled water-quality employees. Rapid-deployment gages, used for floods, could also be used for spills if they included spill-specific sensors. Coordinated expertise at USGS water and environmental science centers can be used for monitoring spill effects and for assessing risk to water quality and ecological communities. • Scientists at the USGS have proven capable of providing science coordination and technical assistance within the Incident Command Structure at the request of the lead on-scene coordinator. This external coordination, as well as internal communication within USGS Water, Hazards, and Ecosystems Mission Areas, could be improved by establishing and naming a USGS spills coordinator. Scott Morlock, Jo Ellen Hinck, and Faith Fitzpatrick are currently (2017) serving in informal coordination roles in addition to their traditional duties.

Open-File Report↗
USGS2009

A proposed origin for fossilized Pennsylvanian plant cuticles by pyrite oxidation (Sydney Coalfield, Nova Scotia, Canada)

Fossilized cuticles, though rare in the roof rocks of coal seam in the younger part of the Pennsylvanian Sydney Coalfield, Nova Scotia, represent nearly all of the major plant groups. Selected for investigation, by methods of Fourier transform infrared spectroscopy (FTIR) and elemental analysis, are fossilized cuticles (FCs) and cuticles extracted from compressions by Schulze's process (CCs) of Alethopteris ambigua. These investigations are supplemented by FTIR analysis of FCs and CCs of Cordaites principalis, and a cuticle-fossilized medullosalean(?) axis. The purpose of this study is threefold: (1) to try to determine biochemical discriminators between FCs and CCs of the same species using semi-quantitative FTIR techniques; (2) to assess the effects chemical treatments have, particularly Schulze's process, on functional groups; and most importantly (3) to study the primary origin of FCs. Results are equivocal in respect to (1); (2) after Schulze's treatment aliphatic moieties tend to be reduced relative to oxygenated groups, and some aliphatic chains may be shortened; and (3) a primary chemical model is proposed. The model is based on a variety of geological observations, including stratal distribution, clay and pyrite mineralogies associated with FCs and compressions, and regional geological structure. The model presupposes compression-cuticle fossilization under anoxic conditions for late authigenic deposition of sub-micron-sized pyrite on the compressions. Rock joints subsequently provided conduits for oxygen-enriched ground-water circulation to initiate in situ pyritic oxidation that produced sulfuric acid for macerating compressions, with resultant loss of vitrinite, but with preservation of cuticles as FCs. The timing of the process remains undetermined, though it is assumed to be late to post-diagenetic. Although FCs represent a pathway of organic matter transformation (pomd) distinct from other plant-fossilization processes, global applicability of the chemical models remains to be tested. CCs and FCs are inferred endpoints on a spectrum of pomd which complicates assessing origin of in-between transformations (partially macerated cuticles). FCs index highly acidic levels that existed locally in the roof rocks.

Bulletin of Geosciences↗
USGS2020

Physical and chemical stressors on algal, invertebrate, and fish communities in 14 Milwaukee area streams, 2004–2013

In 2004, the U.S. Geological Survey (USGS) began sampling 14 wadable streams in urban or urbanizing watersheds near Milwaukee, Wisconsin. The overall goal of the study is to assess the health of the aquatic communities in the Milwaukee Metropolitan Sewerage District planning area to inform current and future watershed management. In addition to collection of biological data on aquatic communities, physical and chemical data were also collected to evaluate effects of potential environmental stressors on the aquatic communities. This fact sheet summarizes the primary results of the study from 2004 to 2013. Detailed information is described in Scudder Eikenberry and others (2020a), and all data are available in Scudder Eikenberry and others (2020b; https://doi.org/10.5066/P9FWMODL ).

Wisconsin↗
USGS1977

Chemical data and variation diagrams of igneous rocks from the Timber Mountain-Oasis Valley Caldera Complex, southern Nevada

Silica variation diagrams presented here are based on 162 chemical analyses of tuffs, lavas, and intrusives, representative of volcanic centers of the Timber Mountain-Oasis Valley caldera complex and cogenetic rocks of the Silent Canyon ca1dera. Most of the volcanic units sampled are shown on the U.S. Geological Survey geologic map of the Timber Mountain caldera area (I-891) and are described in U.S. Geological Survey Professional Paper 919. Early effusives of the complex, although slightly altered, are probably chemically, and petrographically, more like the calc-alkalic Fraction Tuff (Miocene) of the northern Nellis Air Force Base Bombing and Gunnery Range to the north, whereas effusives of later Miocene age, such as the Paintbrush and Timber Mountain Tuffs, are alkali-calcic.

Nevada↗
USGS1997

Agricultural chemicals in Iowa's ground water, 1982-95: What are the trends?

The Iowa Department of Natural Resources. Geological Survey Bureau: the University of Iowa Hygienic Laboratory; and the U.S. Geological Survey (USGS) have been working together to address this question. As part of the Iowa Ground-Water Monitoring Program (IGWM). water samples have been collected from selected Iowa municipal wells since 1982. An examination of this data identified two trends: (1) concentrations of atrazine in Iowa's ground water generally were decreasing over time, and (2) concentrations of metolachlor generally were increasing. Continuing ground-water sampling can determine if these trends represent long-term changes in chemical concentrations.

Iowa↗
USGS2006

Coupling chemical weathering with soil production across soil-mantled landscapes

Soil-covered upland landscapes constitute a critical part of the habitable world. Our understanding of how they evolve as a function of different climatic, tectonic and geological regimes is important across a wide range of disciplines and depends, in part, on understanding the links between chemical and physical weathering processes. Extensive previous work has shown that soil production rates decrease with increasing soil column thickness, but chemical weathering rates were not measured. Here we examine a granitic, soil-mantled hillslope at Point Reyes, California, where soil production rates were determined using in situ produced cosmogenic nuclides ( 10 Be and 26 Al), and we quantify the extent as well as the rates of chemical weathering of the saprolite from beneath soil from across the landscape. We collected saprolite samples from the base of soil pits and analysed them for abrasion pH as well as for major and trace elements by X-ray fluorescence spectroscopy, and for clay mineralogy by X-ray diffraction spectroscopy. Our results show for the first time that chemical weathering rates decrease with increasing soil thickness and account for 13 to 51 per cent of total denudation. We also show that spatial variation in chemical weathering appears to be topographically controlled: weathering rate decreases with slope across the divergent ridge and increases with upslope contributing area in the convergent swale. Furthermore, to determine the best measure for the extent of saprolite weathering, we compared four different chemical weathering indices – the Vogt ratio, the chemical index of alteration (CIA), Parker's index, and the silicon–aluminium ratio – with saprolite pH. Measurements of the CIA were the most closely correlated with saprolite pH, showing that weathering intensity decreases linearly with an increase in saprolite pH from 4·7 to almost 7. Data presented here are among the first to couple directly rates of soil production and chemical weathering with how topography is likely to control weathering at a hillslope scale.

Earth Surface Processes and Landforms↗
USGS2012

Chemicals of emerging concern in water and bottom sediment in Great Lakes areas of concern, 2010 to 2011-Collection methods, analyses methods, quality assurance, and data

The U.S. Geological Survey (USGS) cooperated with the U.S. Environmental Protection Agency and the U.S. Fish and Wildlife Service on a study to identify the occurrence of chemicals of emerging concern (CECs) in water and bottom-sediment samples collected during 2010–11 at sites in seven areas of concern (AOCs) throughout the Great Lakes. Study sites include tributaries to the Great Lakes in AOCs located near Duluth, Minn.; Green Bay, Wis.; Roches­ter, N.Y.; Detroit, Mich.; Toledo, Ohio; Milwaukee, Wis.; and Ashtabula, Ohio. This report documents the collection meth­ods, analyses methods, quality-assurance data and analyses, and provides the data for this study. Water and bottom-sediment samples were analyzed at the USGS National Water Quality Laboratory in Denver, Colo., for a broad suite of CECs. During this study, 135 environmental and 23 field dupli­cate samples of surface water and wastewater effluent, 10 field blank water samples, and 11 field spike water samples were collected and analyzed. Sixty-one of the 69 wastewater indicator chemicals (laboratory method 4433) analyzed were detected at concentrations ranging from 0.002 to 11.2 micrograms per liter. Twenty-eight of the 48 pharmaceuticals (research method 8244) analyzed were detected at concentrations ranging from 0.0029 to 22.0 micro­grams per liter. Ten of the 20 steroid hormones and sterols analyzed (research method 4434) were detected at concentrations ranging from 0.16 to 10,000 nanograms per liter. During this study, 75 environmental, 13 field duplicate samples, and 9 field spike samples of bottom sediment were collected and analyzed for a wide variety of CECs. Forty-seven of the 57 wastewater indicator chemicals (laboratory method 5433) analyzed were detected at concentrations ranging from 0.921 to 25,800 nanograms per gram. Seventeen of the 20 steroid hormones and sterols (research method 6434) analyzed were detected at concentrations ranging from 0.006 to 8,921 nanograms per gram. Twelve of the 20 pharmaceuticals (research method 8244) analyzed were detected at concentrations ranging from 2.35 to 453.5 nanograms per gram. Six of the 11 antidepressants (research method 9008) analyzed were detected at concentrations ranging from 2.79 to 91.6 nanograms per gram.

Great Lakes↗
USGS2008

Methane hydrates

Gas hydrate is a solid, naturally occurring substance consisting predominantly of methane gas and water. Recent scientific drilling programs in Japan, Canada, the United States, Korea and India have demonstrated that gas hydrate occurs broadly and in a variety of forms in shallow sediments of the outer continental shelves and in Arctic regions. Field, laboratory and numerical modelling studies conducted to date indicate that gas can be extracted from gas hydrates with existing production technologies, particularly for those deposits in which the gas hydrate exists as pore-filling grains at high saturation in sand-rich reservoirs. A series of regional resource assessments indicate that substantial volumes of gas hydrate likely exist in sand-rich deposits. Recent field programs in Japan, Canada and in the United States have demonstrated the technical viability of methane extraction from gas-hydrate-bearing sand reservoirs and have investigated a range of potential production scenarios. At present, basic reservoir depressurisation shows the greatest promise and can be conducted using primarily standard industry equipment and procedures. Depressurisation is expected to be the foundation of future production systems; additional processes, such as thermal stimulation, mechanical stimulation and chemical injection, will likely also be integrated as dictated by local geological and other conditions. An innovative carbon dioxide and methane swapping technology is also being studied as a method to produce gas from select gas hydrate deposits. In addition, substantial additional volumes of gas hydrate have been found in dense arrays of grain-displacing veins and nodules in fine-grained, clay-dominated sediments; however, to date, no field tests, and very limited numerical modelling, have been conducted with regard to the production potential of such accumulations. Work remains to further refine: (1) the marine resource volumes within potential accumulations that can be produced through exploratory drilling programs; (2) the tools for gas hydrate detection and characterisation from remote sensing data; (3) the details of gas hydrate reservoir production behaviour through additional, well-monitored and longer duration field tests and (4) the understanding of the potential environmental impacts of gas hydrate resource development. The results of future production tests, in the context of varying market and energy supply conditions around the globe, will be the key to determine the ultimate timing and scale of the commercial production of natural gas from gas hydrates.

Book chapter↗
USGS1972

Subduction zones: Not relevant to present-day problems of waste disposal

SUBDUCTION zones are considered to be sites of disposal for vast areas of the Earth's surface 1 , while new surface is generated simultaneously at rise crests 2 . Bostrom and Sherif 3 suggest that the world's industrial and domestic waste be dumped into subduction zones at deep sea trenches to allow nature to complete the recycling process at geologically rapid rates of 5 to 10 cm/yr. They also point out that trenches are often sites of rapid rates of deposition and suggest that the dumped wastes would, speaking geologically, soon be buried. Francis 4 suggests that canisters of toxic chemical and radioactive wastes could be dumped onto trench sediments and be expected to sink at rates of 20 m/yr, assuming that the mass of turbidites in the trench fill often spontaneously liquefies on shaking by earthquakes. The assumption is based on the supposed lack of evidence for deformed sediment in trenches. I will argue that the suggestion of Bostrom and Sherif 3 is not useful for the next few dozen generations of human populations and will point out observational evidence to show that Francis's 4 assumption is incorrectly founded.

Nature↗
USGS1971

Banquet speech "Man's conquest of energy, its ecological and human consequences"

The world's energy resources suitable for power production are of two classes: (1) various channels of the continuous energy flux from extraterrestrial sources, and from the earth's interior, and (2) chemical, thermal, and nuclear energy stored in the outer part of the lithosphere and in the oceans. The continuous energy influxes are from: solar radiation, 178,000 × 1012 watts; geothermal energy, 32 × 1012 watts; and tidal energy, 3 × 1012 watts. Of the solar energy influx, the only fraction suitable at present for large-scale power production is the approximately 40,000 × 1012 watts expended in evaporation of water and in atmospheric and oceanic circulation. Of this, the world's potential water power is about 2.9 × 1012 watts. A very small fraction of the solar influx, 40 × 1012 watts, is stored chemically by photosynthesis. A minute fraction of this, stored during the geologic past, is the source of the energy of the fossil fuels, coal and petroleum. Tidal power is capable of large-scale development in a small number of coastal localities with a total potential power of about 64,000 megawatts. Of the sources of stored energy, geothermal energy is the least important. Installed capacity by 1970 is about 1,125 electrical megawatts, and the ultimate potential is estimated at about 60,000 megawatts, with a lifetime of probably less than a century. The largest sources of stored energy, other than nuclear, are the fossil fuels. The initial minable world reserves of coal and lignite are estimated to have been about 7.

IEEE Transactions on Nuclear Science↗
USGS2020

Major-element compositional data and thermal data for drill core from Kīlauea Iki lava lake, plus analyses of glasses from scoria of the 1959 summit eruption of Kīlauea Volcano, Hawaii

This report presents electron microprobe data on glasses and selected crystalline phases from Kīlauea Iki lava lake and glasses from the 1959 summit eruption of Kīlauea Volcano, Hawaii. Some of these data have been published previously, but the complete set has not been published before. In addition, this report includes electron microprobe data for phases in melting experiments reported earlier, which form the basis for using many of the glass compositions reported here to estimate quenching temperatures of the samples. Finally, because of the latter application, this report includes all useful field determinations of temperature taken in Kīlauea Iki boreholes from 1967 to 1988. These field measurements have been merged with geothermometry based on glass and Fe-Ti oxide compositions to produce a comprehensive review of all available thermal information for Kīlauea Iki. Making these datasets available completes documentation of field and chemical information on Kīlauea Iki lava lake, supplementing six previous U.S. Geological Survey Open-File Reports listed in the References Cited.

Hawaii↗
USGS1977

GEOTHERM user guide

GEOTHERM is a computerized geothermal resources file developed by the U.S. Geological Survey. The file contains data on geothermal fields, wells, and chemical analyses from the United states and international sources. The General Information Processing System (GIPSY) in the IBM 370/155 computer is used to store and retrieve data. The GIPSY retrieval program contains simple commands which can be used to search the file, select a narrowly defined subset, sort the records, and output the data in a variety of forms. Eight commands are listed and explained so that the GEOTHERM file can be accessed directly by geologists. No programming experience is necessary to retrieve data from the file.

Open-File Report↗
USGS1978

Selected data from thermal-spring areas, southwestern Montana

During 1975-77 the Montana district of the U.S. Geological Survey collected and assembled data describing the flow, temperature, and chemical characteristics of thermal and related waters. The work was part of an assessment of the geothermal resources of southwestern Montana, excluding Yellowstone Park. The purpose of this report is to present representative data from 24 thermal springs and 3 deep wells where water temperatures exceed 38°C (100°F).

Montana↗