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At least 469 records · Page 26Linked to original sources
USGS2010

Monitoring and assessment of ocean acidification in the Arctic Ocean-A scoping paper

Carbon dioxide (CO2) in the atmosphere is absorbed at the ocean surface by reacting with seawater to form a weak, naturally occurring acid called carbonic acid. As atmospheric carbon dioxide increases, the concentration of carbonic acid in seawater also increases, causing a decrease in ocean pH and carbonate mineral saturation states, a process known as ocean acidification. The oceans have absorbed approximately 525 billion tons of carbon dioxide from the atmosphere, or about one-quarter to one-third of the anthropogenic carbon emissions released since the beginning of the Industrial Revolution. Global surveys of ocean chemistry have revealed that seawater pH has decreased by about 0.1 units (from a pH of 8.2 to 8.1) since the 1700s due to absorption of carbon dioxide (Raven and others, 2005). Modeling studies, based on Intergovernmental Panel on Climate Change (IPCC) CO2 emission scenarios, predict that atmospheric carbon dioxide levels could reach more than 500 parts per million (ppm) by the middle of this century and 800 ppm by the year 2100, causing an additional decrease in surface water pH of 0.3 pH units. Ocean acidification is a global threat and is already having profound and deleterious effects on the geology, biology, chemistry, and socioeconomic resources of coastal and marine habitats. The polar and sub-polar seas have been identified as the bellwethers for global ocean acidification.

Open-File Report↗
USGS1995

United States Geological Survey, programs in Nevada

The U.S. Geological Survey (USGS) has been collecting and interpreting natural-resources data in Nevada for more than 100 years. This long-term commitment enables planners to manage better the resources of a State noted for paradoxes. Although Nevada is one of the most sparsely populated States in the Nation, it has the fastest growing population (fig. 1). Although 90 percent of the land is rural, it is the fourth most urban State. Nevada is the most arid State and relies heavily on water resources. Historically, mining and agriculture have formed the basis of the economy; now tourism and urban development also have become important. The USGS works with more than 40 local, State, and other Federal agencies in Nevada to provide natural-resources information for immediate and long-term decisions. Subjects included in this fact sheet: Low-Level Radioactive-Waste Disposal Mining and Water in the Humboldt Basin Aquifer Systems in the Great Basin Water Allocation in Truckee and Carson Basins National Water-Quality Assessment Program Minerals Assessment for Land Management Irrigation Drainage Ground-Water Movement at Nevada Test Site Oil and Gas Resources National Mapping Program Digital Mapping and Aerial Photography Collection of Hydrologlc Data Geologic Mapping Earthquake Hazards Assessing Mineral Resources of the Subsurface Earth Observation Data Cooperative Programs

Nevada↗
USGS2026

The Great Lakes Geologic Mapping Coalition—Working collaboratively to understand the geology of the Great Lakes Region

Introduction The Great Lakes Geologic Mapping Coalition (GLGMC), commonly referred to as the “Coalition,” is a partnership between the U.S. Geological Survey (USGS), the U.S. States of Illinois, Indiana, Michigan, Minnesota, New York, Ohio, Pennsylvania, and Wisconsin and the Canadian province of Ontario. The member States receive funding for geologic mapping work from the USGS National Cooperative Geologic Mapping Program (NCGMP), whereas Ontario participates as a nonfunded partner. The mission of the GLGMC is to produce three-dimensional (3D) geologic maps that depict unconsolidated sediments and near-surface bedrock in the Great Lakes region of North America. Geologic maps are the basis of most earth science investigations and help support resource exploration (energy, minerals, groundwater), natural hazard mitigation, infrastructure development, and land-use planning, all of which can be used to advance economic development and strengthen national security in the Great Lakes region. During the last few million years, the Great Lakes region has experienced repeated glacial advances and retreats, leaving behind extensive sediments, abundant natural resources, and widespread effects on the underlying bedrock geology (Swezey and others, 2022). Linked by shared histories of past glaciations, industrial agriculture, and legacy automotive, coal, steel, and manufacturing industries, the GLGMC member States collaborate to improve the understanding of the 3D distribution of the sediments overlying the region’s bedrock (fig. 1). Developing a comprehensive subsurface 3D framework of this glaciated terrain can provide earth science data to policymakers at all levels. These insights facilitate informed decisions on the exploration, use, and protection of vital resources, such as critical minerals, industrial materials, and aquifers, thereby supporting economic prosperity and the well-being of the citizens of this region. Since its inception in 1998, the Coalition has completed more than 100 geologic mapping projects across the Great Lakes region. Each project aims to deliver geologic maps, 3D datasets, and other information that improves understanding of the geology of the Great Lakes region, with an emphasis on economic and water resources. Key deliverables include 3D geologic maps and models typically portraying sediment thickness, often derived from top-of-bedrock and borehole data. These products are developed through a combination of fieldwork, subsurface modeling, and the collection and analysis of rock and sediment cores. To support Coalition goals, member States collaborate with scientists working on related STATEMAP, EDMAP, and FEDMAP projects. Coalition scientists also engage with Tribal Nations in the Great Lakes region to ensure that Tribal interests pertaining to Coalition work are addressed. Through this collaboration, the Coalition unites the efforts of State, Federal, and Tribal Nation stakeholders to advance geologic data production and enhance understanding of the geologic resources of the Great Lakes region.

Illinois, Indiana, Michigan, Minnesota, New York, ↗
USGS2014

Aquifers of Arkansas: protection, management, and hydrologic and geochemical characteristics of groundwater resources in Arkansas

Sixteen aquifers in Arkansas that currently serve or have served as sources of water supply are described with respect to existing groundwater protection and management programs, geology, hydrologic characteristics, water use, water levels, deductive analysis, projections of hydrologic conditions, and water quality. State and Federal protection and management programs are described according to regulatory oversight, management strategies, and ambient groundwater-monitoring programs that currently (2013) are in place for assessing and protecting groundwater resources throughout the State. Physical attributes, groundwater geochemistry, and groundwater quality are described for each of the 16 aquifers of the State. Information in regard to the hydrology and geochemistry of each of the aquifers is summarized from about 550 historical and recent publications. Additionally, more than 8,000 sites with groundwater-quality data were obtained from the U.S. Geological Survey National Water Information System and the Arkansas Department of Environmental Quality databases and entered into a spatial database to investigate distribution and trends in chemical constituents for each of the aquifers. The 16 aquifers of the State were divided into two major physiographic regions of the State: the Coastal Plain Province (referred to as Coastal Plain) of eastern and southern Arkansas, which includes 11 of the 16 aquifers, and the Interior Highlands Division (referred to as Interior Highlands) of western Arkansas, which includes the remaining 5 aquifers. The 11 aquifers in the Coastal Plain consist of various geologic units that are Cenozoic in age and consist primarily of Cretaceous, Tertiary, and Quaternary sands, gravels, silts, and clays. Groundwater in the Coastal Plain represents one of the most valuable natural resources in the State, driving the economic engines of agriculture, while also supplying abundant water for commercial, industrial, and public-supply use. In terms of age from youngest to oldest, the aquifers of the Coastal Plain include Quaternary alluvial aquifers, including the Mississippi River Valley alluvial aquifer (the most important aquifer in Arkansas in terms of volume of use and economic benefits), the Jackson Group (a regional confining unit that served for decades as an important source of domestic supply), and the Cockfield, Sparta, Cane River, Carrizo, Wilcox, Nacatoch, Ozan, Tokio, and Trinity aquifers. The Mississippi River Valley alluvial aquifer accounts for approximately 94 percent of all groundwater used in the State, and the aquifer is used primarily for irrigation purposes. The Sparta aquifer is the second most important aquifer in terms of use, and the aquifer was used in the past dominantly as a source of public and industrial supply, although increasing irrigation use is occurring because of critically declining water levels in the Mississippi River Valley alluvial aquifer. Other aquifers of the Coastal Plain generally are used as important local sources of domestic, industrial, and public supply, in addition to other minor uses. Water quality generally is good for all aquifers of the Coastal Plain, except for elevated iron concentrations and localized areas of high salinity. The high salinity results from intrusion from underlying formations, evapotranspiration processes in areas of low recharge, and inadequate flushing in downgradient areas of residual salinity from deposition in marine environments. Trends in the spatial distribution of individual chemical constituents are related to position along the flow path for most aquifers of the Coastal Plain. These trends include elevated iron and nitrate concentrations with lower pH values and dissolved solids in groundwater from the outcrop areas, transitioning to lower iron and nitrate (related to changes in redox) and higher pH and dissolved solids (dominantly from the dissolution of carbonate minerals) in groundwater downgradient from outcrop areas. Groundwater generally trended from a calcium- to a sodium-bicarbonate water type with increasing cation exchange along the flow path. The Interior Highlands of western Arkansas has less reported groundwater use than other areas of the State, reflecting a combination of factors. These factors include prevalent and increasing use of surface water, less intensive agricultural uses, lower population and industry densities, lesser potential yield of the resource, and lack of detailed reporting. The overall low yields of aquifers of the Interior Highlands result in domestic supply as the dominant use, with minor industrial, public, and commercial-supply use. Where greater volumes are required for growth of population and industry, surface water is the greatest supplier of water needs in the Interior Highlands. The various aquifers of the Interior Highlands generally occur in shallow, fractured, well-indurated, structurally modified bedrock of this mountainous region of the State, as compared to the relatively flat-lying, unconsolidated sediments of the Coastal Plain. In terms of age from youngest to oldest, the aquifers of the Interior Highlands include: the Arkansas River Valley alluvial aquifer, the Ouachita Mountains aquifer, the Western Interior Plains confining system, the Springfield Plateau aquifer, and the Ozark aquifer. Spatial trends in groundwater geochemistry in the Interior Highlands differ greatly from trends noted for aquifers of the Coastal Plain. In the Coastal Plain, the prevalence of long regional flow paths results in regionally predictable and mappable geochemical changes along the flow paths. In the Interior Highlands, short, topographically controlled flow paths (from hilltops to valleys) within small watersheds represent the predominant groundwater-flow system. As such, dense data coverage from numerous wells would be required to effectively characterize these groundwater basins and define small-scale geochemical changes along any given flow path for aquifers of the Interior Highlands. Changes in geochemistry generally were related to rock type and residence time along individual flow paths. Dominant changes in geochemistry for the Ouachita Mountains aquifer and the Western Interior Plains confining system are attributed to rock/water interaction and changes in redox zonation along the flow path. In these areas, groundwater evolves along flow paths from a calcium- to a sodium-bicarbonate water type with increasing reducing conditions resulting in denitrification, elevated iron and manganese concentrations, and production of methane in the more geochemically evolved and strongest reducing conditions. In the Ozark and Springfield Plateau aquifers, rapid influx of surface-derived contaminants, especially nitrogen, coupled with few to no attenuation processes was attributed to the karst landscape developed on Mississippian- and Ordovician-age carbonate rocks of the Ozark Plateaus. Increasing nitrate concentrations are related to increasing agricultural land use, and areas of mature karst development result in higher nitrate concentrations than areas with less karst features.

Arkasas↗
USGS2015

Coles Hill Uranium Deposit, Virginia, United States, and the Application of UNFC-2009

The case study presented here reviews the uranium resource estimates and summarizes the property situation of the Coles Hill uranium Deposit. Uranium resources at Coles Hill are then classified according to UNFC-2009. The Coles Hill Deposit is located in Pittsylvania County, southern Virginia, United States (Figure 14). Coles Hill was discovered by the Marline Corporation who identified an outcropping surface radiometric anomaly in 1979. The deposit was delineated by Marline and UMETCO (a subsidiary of the Union Carbide Corporation) from 1979 to 1984. In all, 182 rotary holes (38,037 metres (124,799 feet) of drilling) and 74 core holes (19,836 m (65,082 feet) of drilling) were completed and two distinct deposits, the North and South Coles Hill Deposits were defined [66]. Marline let its option to develop the property lapse in response to low uranium prices and a moratorium on uranium mining in Virginia that was passed in 1982. In 2006, a corporation formed by the majority property owner, Virginia Uranium LLC, consolidated 2,296 acres (929 hectares (ha)) in surface rights and 2,940 acres (1,190 ha) in mineral rights, which cover most of the north and south deposits. In 2008, Virginia Uranium drilled 3 core holes and 7 rotary holes. Geophysical surveys were completed for 5 historic holes to confirm earlier results. The Marline core was donated to, and is curated by, the Virginia Natural History Museum; the Marline core is stored on site along with the core drilled in 2008 by Virginia Uranium. The property is accessible from secondary paved roads and the infrastructure, including access to power and water and proximity to local support services, is excellent.

Book chapter↗
USGS2026

The United States Magnetotelluric Array and the National Impedance Map

The United States Magnetotelluric Array (USMTArray) data set, collected in the years 2006–2024, consists of more than 1,700 long-period magnetotelluric stations covering the entirety of the contiguous United States on a quasi-regular 70 km grid. Funding across multiple federal agencies was critical to sustaining this effort to its completion. Important components of the project included active guidance and participation from the MT community, the open and timely availability of all data, and the application of consistent instrumentation and robust data processing. Together with parallel advancement in the development of publicly available three-dimensional (3D) inversion codes, the USMTArray has revitalized the US magnetotelluric community and increased the visibility of magnetotellurics within the Earth-science community. Taken as a whole, these data are visualized as the National Impedance Map, which, together with a 3D synthesis conductivity model of the nation, reveals the electrical architecture of the contiguous US. USMTArray data are used by researchers worldwide for fundamental and applied studies, including investigations of continental architecture and evolution, estimation of hazards to critical infrastructure due to geomagnetic storms, and assessment of the nation's undiscovered geothermal and mineral resources. We here review the history and development of the project, discuss the challenges and successes in its execution, present the National Impedance Map and synthesis conductivity model, and highlight the breadth of research stemming from this rich data set.

conterminous United States↗
USGS1962

Antimony in the United States, exclusive of Alaska and Hawaii

The principal sources of antimony in the United States (exclusive of Alaska and Hawaii) are shown on the accompanying map. The types of deposits are indicated by shape of symbols and the relative importance of the deposits is indicated by size of symbols. In the locality index the localities are listed by States and are keyed by numbers to the map. Localities are distinguished by name of mine, prospect, or geographic area, and their coordinates are given to the nearest minute of latitude and longitude. Geologic relations of each occurrence are characterized briefly. The text and map were compiled from published and unpublished information, and at least one reference is given for each locality if reports on it have been published.

Continental United States↗
USGS2017

Rhenium

Rhenium is one of the rarest elements in Earth’s continental crust; its estimated average crustal abundance is less than 1 part per billion. Rhenium is a metal that has an extremely high melting point and a heat-stable crystalline structure. More than 80 percent of the rhenium consumed in the world is used in high-temperature superalloys, especially those used to make turbine blades for jet aircraft engines. Rhenium’s other major application is in platinum-rhenium catalysts used in petroleum refining. Rhenium rarely occurs as a native element or as its own sulfide mineral; most rhenium is present as a substitute for molybdenum in molybdenite. Annual world mine production of rhenium is about 50 metric tons. Nearly all primary rhenium production (that is, rhenium produced by mining rather than through recycling) is as a byproduct of copper mining, and about 80 percent of the rhenium obtained through mining is recovered from the flue dust produced during the roasting of molybdenite concentrates from porphyry copper deposits. Molybdenite in porphyry copper deposits can contain hundreds to several thousand grams per metric ton of rhenium, although the estimated rhenium grades of these deposits range from less than 0.1 gram per metric ton to about 0.6 gram per metric ton. Continental-arc porphyry copper-(molybdenum-gold) deposits supply most of the world’s rhenium production and have large inferred rhenium resources. Porphyry copper mines in Chile account for about 55 percent of the world’s mine production of rhenium; rhenium is also recovered from porphyry copper deposits in the United States, Armenia, Kazakhstan, Mexico, Peru, Russia, and Uzbekistan. Sediment-hosted strata-bound copper deposits in Kazakhstan (of the sandstone type) and in Poland (of the reduced-facies, or Kupferschiefer, type) account for most other rhenium produced by mining. These types of deposits also have large amounts of identified rhenium resources. The future supply of rhenium is likely to depend largely on the capacity of the specialized processing facilities needed to recover rhenium from molybdenite concentrates. The environmental consequences of rhenium recovery are closely linked to the consequences of mining large porphyry copper and strata-bound copper deposits; no additional environmental impact from recovery of rhenium from these deposits has been identified. No information is available regarding the potential toxic effects of rhenium on humans, partly because of the low natural abundance of rhenium.

Professional Paper↗
USGS2001

Assessment method for epithermal gold deposits in northeast Washington State using weights-of-evidence GIS modeling

The weights-of-evidence analysis, a quantitative mineral resource mapping tool, is used to delineate favorable areas for epithermal gold deposits and to predict future exploration activity of the mineral industry for similar deposits in a four-county area (222 x 277 km), including the Okanogan and Colville National Forests of northeastern Washington. Modeling is applied in six steps: (1) building a spatial digital database, (2) extracting predictive evidence for a particular deposit, based on an exploration model, (3) calculating relative weights for each predictive map, (4) combining the geologic evidence maps to predict the location of undiscovered mineral resources and (5) measuring the intensity of recent exploration activity by use of mining claims on federal lands, and (6) combining mineral resource and exploration activity into an assessment model of future mining activity. The analysis is accomplished on a personal computer using ArcView GIS platform with Spatial Analyst and Weights-of-Evidence software. In accord with the descriptive model for epithermal gold deposits, digital geologic evidential themes assembled include lithologic map units, thrust faults, normal faults, and igneous dikes. Similarly, geochemical evidential themes include placer gold deposits and gold and silver analyses from stream sediment (silt) samples from National Forest lands. Fifty mines, prospects, or occurrences of epithermal gold deposits, the training set, define the appropriate a really-associated terrane. The areal (or spatial) correlation of each evidential theme with the training set yield predictor theme maps for lithology, placer sites and normal faults. The weights-of-evidence analysis disqualified the thrust fault, dike, and gold and silver silt analyses evidential themes because they lacked spatial correlation with the training set. The decision to accept or reject evidential themes as predictors is assisted by considering probabilistic data consisting of weights and contrast values calculated for themes according to areal correlation with the training sites. Predictor themes having acceptable weights and contrast values are combined into a preliminary model to predict the locations of undiscovered epithermal gold deposits. This model facilitates ranking of tracts as non-permissive, permissive or favorable categories based on exclusionary, passive, and active criteria through evaluation of probabilistic data provided by interaction of predictor themes. The method is very similar to the visual inspection method of drawing conclusions from anomalies on a manually overlain system of maps. This method serves as a model for future mineral assessment procedures because of its objective nature. To develop a model to predict future exploration activity, the locations of lode mining claims were summarized for 1980, 1985, 1990, and 1996. Land parcels containing historic claims were identified either as those with mining claims present in 1980 or valid claims present in 1985. Current claim parcels were identified as those containing valid lode claims in either 1990 or 1996. A consistent parcel contains both historic and current claims. The epithermal gold and mining claim activity models were combined into an assessment (or mineral resource-activity) model to assist in land use decisions by providing a prediction of mineral exploration activity on federal land in the next decade. Ranks in the assessment model are: (1) no activity, (2) low activity, (3) low to moderate activity, (4) moderate activity and (5) high activity.

Washington↗
USGS2013

USGS Arctic Ocean carbon cruise 2010: field activity H-03-10-AR to collect carbon data in the Arctic Ocean, August - September 2010

Carbon dioxide (CO 2 ) in the atmosphere is absorbed at the surface of the ocean by reacting with seawater to form carbonic acid, a weak, naturally occurring acid. As atmospheric carbon dioxide increases, the concentration of carbonic acid in seawater also increases, causing a decrease in ocean pH and carbonate mineral saturation states, a process known as ocean acidification. The oceans have absorbed approximately 525 billion tons of carbon dioxide from the atmosphere, or about one-quarter to one-third of the anthropogenic carbon emissions released since the beginning of the Industrial Revolution (Sabine and others, 2004). Global surveys of ocean chemistry have revealed that seawater pH has decreased by about 0.1 units (from a pH of 8.2 to 8.1) since the 1700s due to absorption of carbon dioxide (Caldeira and Wickett, 2003; Orr and others, 2005; Raven and others, 2005). Modeling studies, based on Intergovernmental Panel on Climate Change (IPCC) CO 2 emission scenarios, predict that atmospheric carbon dioxide levels could reach more than 500 parts per million (ppm) by the middle of this century and 800 ppm by the year 2100, causing an additional decrease in surface water pH of 0.3 pH units. Ocean acidification is a global threat and is already having profound and deleterious effects on the geology, biology, chemistry, and socioeconomic resources of coastal and marine habitats (Raven and others, 2005; Ruttiman, 2006). The polar and sub-polar seas have been identified as the bellwethers for global ocean acidification.

Data Series↗
USGS2013

USGS Arctic Ocean carbon cruise 2011: field activity H-01-11-AR to collect carbon data in the Arctic Ocean, August - September 2011

Carbon dioxide (CO 2 ) in the atmosphere is absorbed at the surface of the ocean by reacting with seawater to form a weak, naturally occurring acid called carbonic acid. As atmospheric carbon dioxide increases, the concentration of carbonic acid in seawater also increases, causing a decrease in ocean pH and carbonate mineral saturation states, a process known as ocean acidification. The oceans have absorbed approximately 525 billion tons of carbon dioxide from the atmosphere, or about one-quarter to one-third of the anthropogenic carbon emissions released since the beginning of the Industrial Revolution (Sabine and others, 2004). Global surveys of ocean chemistry have revealed that seawater pH has decreased by about 0.1 units (from a pH of 8.2 to 8.1) since the 1700s due to absorption of carbon dioxide (Caldeira and Wickett, 2003; Orr and others, 2005; Raven and others, 2005). Modeling studies, based on Intergovernmental Panel on Climate Change (IPCC) CO 2 emission scenarios, predict that atmospheric carbon dioxide levels could reach more than 500 parts per million (ppm) by the middle of this century and 800 ppm by the year 2100, causing an additional decrease in surface water pH of 0.3 pH units. Ocean acidification is a global threat and is already having profound and deleterious effects on the geology, biology, chemistry, and socioeconomic resources of coastal and marine habitats (Raven and others, 2005; Ruttiman, 2006). The polar and sub-polar seas have been identified as the bellwethers for global ocean acidification.

Data Series↗
USGS1962

Chromite in the United States, exclusive of Alaska and Hawaii

The chromite deposits in the United States (exclusive of Alaska and Hawaii) are shown on the accompanying map. In compiling the map, the deposits were classified in five size categories according to the estimated total quantity of chromite present before mining. The map shows, by different symbols, deposits of chromite in ultramafic rocks, beach sands in which chromite is an important constituent, and lateritic iron ores in which chromium has been concentrated by weathering of peridotite in situ. Although geologically significant amounts of chromium are known to occur in some gabbros and sedimentary rocks other than beach sands and laterite, the data are too fragmentary to show on the map.

Mineral Investigations Resource Map↗
USGS1980

Thorium resources of selected regions in the United States

Thorium resources have been assessed in a previous report entitled 'Principal thorium resources in the United States' (Staatz and others, 1979) for (1) veins in the larger districts, {2) massive carbonatites, {3) disseminated deposits, and {4) stream placers of North and South Carolina. This report is a sequel to that report and assesses thorium resources in {1) Florida beach placers, (2) Idaho stream placers, (3) veins and pipes in the Bokan Mountain district, Alaska, (4) carbonatite dikes, and {5) apatite-bearing iron deposits near Mineville, New York. Thorium resources for each of these categories are divided into reserves and probable potential resources. When data are available, each of these is then divided into the following cost categories: (1) the amount of ThO2 producible at a cost of less than $15/lb (per pound), (2) the amount producible at a cost of between $15 and $30/lb, and (3) the amount producible at a cost of between $30 and $50/1b. Beach placers of northern Florida have reserves of 16,200 short tons of ThO2 and probable potential resources of 5,120 tons of ThO2. These deposits are heavy-mineral placers that are mined for a variety of minerals--principally titanium minerals and zircon. The thorium-bearing mineral in these placers, monazite, makes up only a minor part of the heavy minerals. Therefore, production of ThO2 from these placers is dependent on the markets for other heavy minerals. Assuming the market for other heavy minerals to be the same as in 1978, then 98 percent of the ThO2 could be produced for less than $15/lb. If, however, no other coproducts were produced, then the cost of producing ThO2 would be greater than $50/1b. Stream placers containing thorium are found along many streams that drain the Idaho batholith, but most are too small to add significantly to the thorium resources. The resources of the five largest districts, each of which consists of at least several individual placers, have been tabulated. These districts are (1) Long Valley, (2) Bear Valley, (3) Burgdorf-Warren area, (4) Boise Basin, and (5) Ell City-Newsome area. These five areas have reserves of 10,100 short tons of ThO2 and probable potential resources of 10,300 tons. Long Valley contains about half the reserves--5,680 tons of ThO2--and all the probable potential resources. Monazite is the most important heavy mineral in all except the Bear Valley deposit. Here euxenite, although not quite as abundant as monazite, is a more important mineral, because it contains approximately 14.5 percent U3O8 in addition to 5 percent ThO2. Reserves in this placer amount to 1,605 short tons of ThO2 and 1,475 tons of U3O8. Eighty-two percent of the reserves and all of the probable potential resources can be produced at less than $30/1b of ThO2. The lower cost reserves are concentrated in the Long and Bear Valley areas. Here 64 percent of the ThO2 can be produced for less than $15/1b and another 29 percent of the ThO2 at between $15 and $30/lb. Sixteen veins and pipelike bodies are evaluated in the Bokan Mountain area of southeastern Alaska. The district contains other deposits that are too poorly exposed to make meaningful resource estimates. Reserves estimated in this district are 1,440 short tons of ThO2; probable potential resources amount to 2,320 tons of ThO2. About 99 percent of these resources are in deposits whose grade is at least 0.2 percent ThO2. In addition, these deposits contain reserves of 420 tons of U3O8 and probable potential resources of 820 tons of U3O8. Eighty-two percent of the reserves and probable potential resources can be produced at less than $15/lb. The average grade of this ore is 0.54 percent ThO2 and 0 15 percent U3O8. Some carbonatite dikes, although generally not as high grade as the veins, contain resources of thorium. Carbonatite dikes in the following six districts were investigated: (1) Wet Mountains, Colo.; (2) Powderhorn district, Colorado; (3) Mountain Pass area, California; (4) Bearpaw

Circular↗
USGS1967

Iron in the United States, exclusive of Alaska and Hawaii

The iron-ore deposits in the United States (exclusive of Alaska and Hawaii) are shown on the accompanying map; many iron-bearing deposits that are of lesser or only potential value are also shown. Because these deposits range widely in extent, two general categories of symbols are used, each of which is subdivided as explained below. The first category is for deposits of such restricted extent that they can be represented by a "spot": the second is for deposits which, although not necessarily extremely large in terms of volume or tonnage, are either continuous (or essentially so) or clustered in reasonably well-defined districts of numerous small occurrences.

Mineral Investigations Resource Map↗
USGS1875

Preliminary report upon a reconnaissance through southern and southeastern Nevada, made in 1869

By authority from headquarters Military Division of the Pacific, Lieut. George M. Wheeler, United States Engineers, will proceed with his civil assistants and three enlisted men to either Camps Halleck or Ruby, Nevada, and having been joined by Lieut. D.W. Lockwood, United States Engineers, now en route via Fort Churchill, will there organize a party, to consist of two-non-commissioned officers and twenty-three enlisted men, (cavalry, or infantry mounted,) such drivers, packers, and guides as may be required; equip them with the necessary, full, and complete outfit, as far as the resources of the posts will enable him so to do; after which he will proceed, via the White Pine district, to make a thorough and careful reconnaissance of the district of country to the south and east of White Pine, extending thereto from the White Pine or Grant district, of obtaining correct data for a military map of the country, and for the selection of the site or sites for such military post or posts to cover the mining country south and east of White Pine from hostile Indians, as may be required. Such explorations and examinations as may will be made in reference to the physical geography of the country, its resources in wood, water, agricultural or mineral productions. The character, habits, and numbers of Indian tribes, and their dispositions toward settlers and miners, will be subjects for investigations.

Nevada↗
USGS2020

Statewide assessment of karst aquifers in New York with an inventory of closed-depression and focused-recharge features

Karst is a landscape formed from the dissolution of soluble rock or rock containing minerals that are easily dissolved from within the rock. The landscape is characterized by sinkholes, caves, losing streams, springs, and underground drainage systems, which rapidly move water through the karst. The two forms of karst in New York State include carbonate karst, which forms in carbonate rock (limestone, marble, and dolostone), and evaporite karst, which forms in rock that contains the evaporite minerals gypsum and halite. Past and recent studies of karst across the State have shown that areas of focused recharge in karstic carbonate rock allow contaminants to enter aquifer systems with little attenuation. Focused areas of recharge need to be identified to help prevent such contamination from sources on or adjacent to the karst. The New York State Departments of Environmental Conservation and Health are collaborating with the agricultural community to make farmers and farm-planning advisors more aware of karst and how to manage daily farming activities to reduce their impact on surface water and groundwater resources, especially in karst areas. There is also a need to make regulators, planners, and the general public aware of New York’s karst resources and to properly protect and manage these resources to protect the quality of groundwater and surface water that can flow into, through, and from karst bedrock. Using publicly available geospatial data, karst bedrock and closed depressions over or near karst rock were identified across New York. Carbonate, evaporite, and marble geologic units were selected from a statewide 1:250,000-scale bedrock geology dataset. The selected geologic units were intersected with 7.5-minute quadrangle maps to define the study area. The U.S. Geological Survey has compiled an inventory of closed depressions from statewide digital contour data, scanned 7.5-minute topographic maps known as a digital raster graphics, and light detection and ranging (lidar) digital elevation models. Analysis of the data resulted in the identification of 5,023 closed depressions statewide. The inventory was conducted to eliminate duplication of results from analysis of the three data sources. A series of overlay analyses was conducted using the closed depressions and thematic data known to be key factors in determining the probability of a closed depression contributing to focused groundwater recharge; the thematic data include bedrock geology, soil type, soil infiltration rate, and land cover. Though the extent of karst development is important in understanding the interaction between surface water and groundwater in karst terrains, some of the worst cases of groundwater contamination in karst can occur where only minor karst features might be present. The presence of karst—be it a short section of a solutioned fracture or an extensive cave system—requires careful consideration, forward-looking environmental planning, and consistent water-quality protection to preserve New York State’s water resources.

New York↗
USGS2014

Mineral resource of the month: Iron and steel

Iron is one of the most abundant elements on Earth, but it does not occur in nature in a useful metallic form. Although ancient people may have recovered some iron from meteorites, it wasn’t until smelting was invented that iron metal could be derived from iron oxides. After the beginning of the Iron Age in about 1200 B.C., knowledge of iron- and steelmaking spread from the ancient Middle East through Greece to the Roman Empire, then to Europe and, in the early 17th century, to North America. The first successful furnace in North America began operating in 1646 in what is now Saugus, Mass. Introduction of the Bessemer converter in the mid-19th century made the modern steel age possible. Pig iron is a high-carbon alloy made by smelting iron ore in a blast furnace with carbonaceous material, typically coke, as a reducing agent. Limestone is added to the iron ore-coke charge as a fluxing agent to remove impurities. Steel is produced from pig iron by removing some of the carbon in a basic oxygen converter and adding several alloying elements, such as manganese, chromium, copper, nickel, titanium, molybdenum, tungsten and vanadium. Steel is also made by recycling ferrous scrap in an electric arc furnace. There are many grades of steel, but the three major types of steel are carbon, alloy and stainless. About 93 percent of the steel made in the United States is carbon steel, which contains a maximum 2 percent carbon. Applications are found in appliances, construction, shipbuilding, containers and packaging, as well as in the automotive, machinery and equipment industries. Alloy steel, about 5 percent of annual production, contains as much as 4 percent alloying elements. Special applications for alloy steel include use in machined parts and tool fabrication. Stainless steel, which accounts for about 2 percent of annual steel production, is formed by adding chromium and usually nickel to steel to make it highly corrosion-resistant. Since 2008, steelmaking capacity has greatly exceeded apparent steel consumption, primarily as a result of China’s rapid economic expansion and rapidly increasing capacity. This has resulted in an influx of steel products into the United States and other steelmaking countries that already have excess capacity. Demand by China’s steelmakers has also driven unprecedented increases in the prices of iron ore and metallurgical coal. In the short term, steelmaking capacity, globally and especially in China, is expected to continue to exceed steel consumption, with steel prices and production costs remaining stable.

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USGS1965

Barite in the United States, exclusive of Alaska and Hawaii

The mineral barite, barium sulfate, is the chief source of barium and its compounds needed for many industrial processes and products. Barite is found the world over and is abundant and widely distributed throughout the United States. The barite deposits of the United States (exclusive of Alaska and Hawaii) are shown on the accompanying map. The principal geologic type of deposit is indicated by the shape of symbol and the relative importance of the deposit is indicated by the size of symbol. This text lists localities by State, and index numbers are keyed to the map. Localities are distinguished by name of mine, prospect, or geographic area; their coordinates are given to the nearest minute of latitude and longitude. Geologic relations of each occurrence, if known, are summarized briefly. The text and map were compiled from published and unpublished information, and at least one reference is given for each locality, if reports have been published. The listings in some States are preceded by a principal reference which is a major source of information about deposits in those States.

Mineral Investigations Resource Map↗