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USGS2017

Annual review 2016: Exploration review

This summary of international mineral exploration activities for the year 2016 draws upon information from industry sources, published literature, SNL Metals & Mining (SNL), an offering of S&P Global Market Intelligence (New York, NY), and specialists in the U.S. Geological Survey (USGS) National Minerals Information Center. Three types of information are reported and analyzed in this annual review of international exploration: 1) budgetary statistics expressed in U.S. dollars provided by SNL; 2) regional and site-specific exploration activities that took place in 2016 as compiled by the USGS and 3) regional events and legislation that affected exploration activities including economic, social and political conditions, which were derived from published sources and discussions with USGS and industry specialists. Commodity and regional compilations are presented in this summary. Because multiple sources were used to develop commodity and regional compilations, statistics may vary depending on the source and type of data that are being reported.

Mining Engineering↗

USGS2005

Chapter K: Progress in the Evaluation of Alkali-Aggregate Reaction in Concrete Construction in the Pacific Northwest, United States and Canada

The supply of aggregates suitable for use in construction and maintenance of infrastructure in western North America is a continuing concern to the engineering and resources-management community. Steady population growth throughout the region has fueled demand for high-quality aggregates, in the face of rapid depletion of existing aggregate resources and slow and difficult permitting of new sources of traditional aggregate types. In addition to these challenges, the requirement for aggregates to meet various engineering standards continues to increase. In addition to their physical-mechanical properties, other performance characteristics of construction aggregates specifically depend on their mineralogy and texture. These properties can result in deleterious chemical reactions when aggregate is used in concrete mixes. When this chemical reaction-termed 'alkali-aggregate reaction' (AAR)-occurs, it can pose a major problem for concrete structures, reducing their service life and requiring expensive repair or even replacement of the concrete. AAR is thus to be avoided in order to promote the longevity of concrete structures and to ensure that public moneys invested in infrastructure are well spent. Because the AAR phenomenon is directly related to the mineral composition, texture, and petrogenesis of the rock particles that make up aggregates, an understanding of the relation between the geology and the performance of aggregates in concrete is important. In the Pacific Northwest, some aggregates have a moderate to high AAR potential, but many others have no or only a low AAR potential. Overall, AAR is not as widespread or serious a problem in the Pacific Northwest as in other regions of North America. The identification of reactive aggregates in the Pacific Northwest and the accurate prediction of their behavior in concrete continue to present challenges for the assessment and management of geologic resources to the owners and operators of pits and quarries and to the users of the concrete aggregates mined from these deposits. This situation is complicated by the length of time typically required for AAR to become noticeable in concrete construction in the Pacific Northwest, commonly on such a scale that other deterioration mechanisms may have masked the effects of AAR. Distinguishing between the effects of AAR and those related to other problems in concrete is important for understanding the nature and severity of AAR throughout the Pacific Northwest. Furthermore, developing an understanding of the extent of the problem will assist efforts to maximize the intelligent and stewardly use of aggregate resources in the Pacific Northwest. This chapter illustrates the current 'state of the art' of AAR studies in the Pacific Northwest, a region with a common geologic heritage as well as many distinct geologic elements. The optimal use of aggregates in the construction of concrete structures that will achieve their design life is possible through an understanding of the engineering and geologic properties of these aggregates and of their geologic setting.

Bulletin↗

USGS2012

Stratiform chromite deposit model

A new descriptive stratiform chromite deposit model was prepared which will provide a framework for understanding the characteristics of stratiform chromite deposits worldwide. Previous stratiform chromite deposit models developed by the U.S. Geological Survey (USGS) have been referred to as Bushveld chromium, because the Bushveld Complex in South Africa is the only stratified, mafic-ultramafic intrusion presently mined for chromite and is the most intensely researched. As part of the on-going effort by the USGS Mineral Resources Program to update existing deposit models for the upcoming national mineral resource assessment, this revised stratiform chromite deposit model includes new data on the geological, mineralogical, geophysical, and geochemical attributes of stratiform chromite deposits worldwide. This model will be a valuable tool in future chromite resource and environmental assessments and supplement previously published models used for mineral resource evaluation. Stratiform chromite deposits are found throughout the world, but the chromitite seams of the Bushveld Complex, South Africa, are the largest and most intensely researched. The chromite ore is located primarily in massive chromitite seams and, less abundantly, in disseminated chromite-bearing layers, both of which occur in the ultramafic section of large, layered mafic-ultramafic stratiform complexes. These mafic-ultramafic intrusions mainly formed in stable cratonic settings or during rift-related events during the Archean or early Proterozoic, although exceptions exist. The chromitite seams are cyclic in nature as well as laterally contiguous throughout the entire intrusion. Gangue minerals include olivine, pyroxenes (orthopyroxene and clinopyroxene), plagioclase, sulfides (pyrite, chalcopyrite, pyrrhotite, pentlandite, bornite), platinum group metals (mainly laurite, cooperite, braggite), and alteration minerals. A few deposits also contain rutile and ilmenite. The alteration phases include serpentine, chlorite, talc, magnetite, kaemmererite, uvarovite, hornblende, and carbonate minerals, such as calcite and dolomite. Stratiform chromite deposits are primarily hosted by peridotites, harzburgites, dunites, pyroxenites, troctolites, and anorthosites. Although metamorphism may have altered the ultramafic regions of layered intrusions postdeposition, only igneous processes are responsible for formation. From a diagnostic standpoint and for assessment purposes, they have no temporal or spatial relation to sedimentary rocks. The exact mechanisms responsible for the development of stratiform chromite deposits and the large, layered mafic-ultramafic intrusions where they are found are highly debated. The leading argument postulates that a parent magma mixed with a more primitive magma during magma chamber recharge. The partially differentiated magma could then be forced into the chromite stability field, resulting in the massive chromitite layers found in stratiform complexes. Contamination of the parent magma by localized assimilation of felsic country rock at the roof of the magma chamber has also been proposed as a mechanism of formation. Others suggest that changes in pressure or oxygen fugacity may be responsible for the occurrence of massive chromitite seams in layered mafic, ultramafic intrusions. The massive chromitite layers contain high levels of chromium and strong associations with platinum group elements. Anomalously high magnesium concentrations as well as low sodium, potassium, and phosphorus concentrations are also important geochemical features of stratiform chromite deposits. The presence of orthopyroxenite in many of the deposits suggests high silica and high magnesium concentrations in the parent magma. Most environmental concerns associated with the mining and processing of chromite ore focus on the solubility of chromium and its oxidation state. Although trivalent chromium (Cr 3+ ) is an essential micronutrient for humans, hexavalent chromium (Cr 6+ ) is highly toxic. Chromium-bearing solid phases that occur in the chromite ore-processing residue, for example, can effect the geochemical behavior and oxidation state of chromium in the environment.

Scientific Investigations Report↗

USGS2002

Relationship of the 1999 Hector Mine and 1992 Landers fault ruptures to offsets on neogene faults and distribution of late Cenozoic basins in the eastern California shear zone

This report examines the Hector Mine and Landers earthquakes in the broader context of faults and fault-related basins of the eastern California shear zone (ECSZ). We compile new estimates of total strike-slip offset (horizontal separation) at nearly 30 fault sites based on offset magnetic anomaly pairs. We also present a map of the depth to pre-Cenozoic basement rock (thickness of basin-filling late Cenozoic deposits) for the region, based on an inversion of gravity and geologic data. Our estimates of total long-term strike-slip offsets on faults that slipped during the 1999 Hector Mine (3.4 km), and the 1992 Landers earthquakes (3.1 ? to 4.6 km) fall within the 3- to 5-km range of total strike-slip offset proposed for most faults of the western ECSZ. Faults having offsets as great as 20 km are present in the eastern part of the ECSZ. Although the Landers rupture followed sections of a number of faults that had been mapped as independent structures, the similarity in total strike-slip offset associated with these faults is compatible with one of the following hypotheses: (1) the Landers multistrand rupture is a typical event for this linked fault system or (2) this complex rupture path has acted as a coherent entity when viewed over some characteristic multiearthquake cycle. The second hypothesis implies that, for each cycle, slip associated with smaller earthquakes on individual fault segments integrates to a uniform slip over the length of the linked faults. With one exception, the region surrounding the Hector Mine and Landers ruptures is devoid of deep late Cenozoic basins. In particular, no deep basins are found immediately north of the Pinto Mountain fault, a place where a number of kinematic models for development of the ECSZ have predicted basins. In contrast, some basins exist near Barstow and along the eastern part of the ECSZ, where the model of Dokka et al. (1998) predicts basins.

Bulletin of the Seismological Society of America↗

USGS2011

Mineral resource of the month: feldspar

The article focuses on feldspar, a mineral that composes of potassium, sodium, or a fusion of the two, and its various applications. According to estimates by scientists, the mineral is present at 60 percent of the crust of Earth, wherein it is commonly used for making glass and ceramics. Global mining of feldspar was about 20 million metric tons in 2010, wherein Italy, Turkey, and China mine 55 percent of the feldspar worldwide.

Earth↗

USGS1946

Copper deposits at the Rush and Brown mine and Venus prospect, Prince of Wales Island, southeastern Alaska

The Rush and Brown mine and the Venus prospect are near the head of Kasaan Bay about 10 miles northwest of the village of Kasaan and about 45 miles northwest of Ketchikan, the nearest port. (See fig. 1.) They are in an area of moderate relief in in which some hills are a little more than 500 feet high. Much of the area is covered with glacial drift and dense vegetation. Muskegs are numerous. Outcrops are scarce and are confined mostly to steep slopes, stream beds, and places where development work has been done on the ore deposits. Topographic, geologic, and magnetic surveys of the vicinities of the ore deposits were made by the Geological Survey in 1943, and a brief examination of a portion of the underground workings at the Rush and Brown mine was made in 1944. The area is underlain principally by greenstone which has been intruded by bodies of pyroxenite, gabbro, and diorite. Foliation in the greenstone is obscure. post of the intrusive bodies trend northwesterly. The principal ore deposits are veins containing chiefly pyrite, chalcopyrite, and pyrrhotite. A few deposits of copper-bearing magnetite have been found. Most of these are small, but a larger one at the Rush and Brown mine has been mined for its copper and precious metals.

Alaska↗

USGS2003

Geochemistry, geochronology, mineralogy, and geology suggest sources of and controls on mineral systems in the southern Toquima Range, Nye County, Nevada

Geochemistry maps showing the distribution and abundance of 18 elements in about 1,400 rock samples, both mineralized and unmineralized, from the southern Toquima Range, Nev., indicate major structural and lithologic controls on mineralization, and suggest sources of the elements. Radiometric age data, lead mineralogy and paragenesis data, and lead-isotope data supplement the geochemical and geologic data, providing further insight into timing, sources, and controls on mineralization. Major zones of mineralization are centered on structural margins of calderas and principal northwest-striking fault zones, as at Round Mountain, Manhattan, and Jefferson mining districts, and on intersections of low-angle and steep structures, as at Belmont mining district. Paleozoic sedimentary rocks, mostly limestones (at Manhattan, Jefferson, and Belmont districts), and porous Oligocene ash-flow tuffs (at Round Mountain district) host the major deposits, although all rock types have been mineralized as evidenced by numerous prospects throughout the area. Principal mineral systems are gold-silver at Round Mountain where about 7 million ounces of gold and more than 4 million ounces of silver has been produced; gold at Gold Hill in the west part of the Manhattan district where about a half million ounces of gold has been produced; gold-mercury-arsenic-antimony in the east (White Caps) part of the Manhattan district where a few hundred thousand ounces of gold has been produced; and silver-lead-antimony at Belmont where more than 150,000 ounces of silver has been produced. Lesser amounts of gold and silver have been produced from the Jefferson district and from scattered mines elsewhere in the southern Toquima Range. A small amount of tungsten was produced from mines in the granite of the Round Mountain pluton exposed east of Round Mountain, and small amounts of arsenic, antimony, and mercury have been produced elsewhere in the southern Toquima Range. All elements show unique distribution patterns that suggest specific sources and lithologic influences on deposition, as well as multiple episodes of mineralization. Principal episodes of mineralization are Late Cretaceous (molybdenum and tungsten in and near granite; silver at Belmont and Silver Point mines), early Oligocene [tourmaline and base- and precious-metals around the granodiorite of Dry Canyon stock as well as at Manhattan(?)], late Oligocene (gold at Round Mountain and Jefferson), and Miocene (gold at Manhattan). Most likely principal sources of molybdenum, tungsten, silver, and bismuth are Cretaceous granites; of antimony, arsenic, and mercury are intermediate-composition early Oligocene intrusives; and of gold are early and late Oligocene and early Miocene magmas of the volcanic cycle. Lead may have been derived principally from Cretaceous granitic magma and Paleozoic sedimentary rocks. Several areas prospective for undiscovered mineral deposits are suggested by spatial patterns of element distributions related to geologic features. The Manhattan district in the vicinity of the White Caps mine may be underlain by a copper-molybdenum porphyry system related to a buried stock; peripheral high-grade gold veins and skarn deposits may be present below deposits previously mined. The Jefferson district also may be underlain by a copper-molybdenum porphyry system related to a buried stock, it too with peripheral high-grade gold deposits. The Bald Mountain Canyon belt of small gold veins has potential for deeper deposits in buried porous ash-flow tuff similar to the huge Round Mountain low-grade gold-silver deposit. Several other areas have potential for a variety of mineral deposits. Altogether the geochemical, geochronologic, mineralogic, and geologic evidence suggests recurring mineralizing episodes of varied character, from Late Cretaceous to late Tertiary time, related to a long-lived hot spot deep in the crust or in the upper mantle. Granite plutons of Late Cretaceous age were minerali

Nevada↗

USGS1920

The r and s molybdenum mine, Toas County, New Mexico

No abstract available.

New Mexico↗

USGS2008

Understanding contaminants associated with mineral deposits

Interdisciplinary studies by the U.S. Geological Survey (USGS) have resulted in substantial progress in understanding the processes that control the release of metals and acidic water from inactive mines and mineralized areas, the transport of metals and acidic water to streams, and the fate and effect of metals and acidity on downstream ecosystems. The potential environmental effects associated with abandoned and inactive mines, resulting from the complex interaction of a variety of chemical and physical processes, is an area of study that is important to the USGS Mineral Resources Program. Understanding the processes contributing to the environmental effects of abandoned and inactive mines is also of interest to a wide range of stakeholders, including both those responsible for managing lands with historically mined areas and those responsible for anticipating environmental consequences of future mining operations. The recently completed (2007) USGS project entitled 'Process Studies of Contaminants Associated with Mineral Deposits' focused on abandoned and inactive mines and mineralized areas in the Rocky Mountains of Montana, Colorado, New Mexico, Utah, and Arizona, where there are thousands of abandoned mines. Results from these studies provide new information that advances our understanding of the physical and biogeochemical processes causing the mobilization, transport, reaction, and fate of potentially toxic elements (including aluminum, arsenic, cadmium, copper, iron, lead, and zinc) in mineralized near-surface systems and their effects on aquatic and riparian habitat. These interdisciplinary studies provide the basis for scientific decisionmaking and remedial action by local, State, and Federal agencies charged with minimizing the effects of potentially toxic elements on the environment. Current (2007) USGS research highlights the need to understand (1) the geologic sources of metals and acidity and the geochemical reactions that release them from their sources, (2) the pathways that facilitate transport from those sources, and (3) the processes that control the fate of the elements once released from the sources. Experts in the fields of economic geology, structural geology, mineralogy, geophysics, geochemistry, hydrology, ground-water modeling, microbiology, and toxicology came together for a series of studies that address these relationships on scales ranging from the microscopic to the watershed. This Circular presents results and highlights from the detailed, interdisciplinary studies that include investigations in both mining-affected areas and mineralized but unmined areas. The first section of the Circular describes laboratory and site-scale field investigations that primarily focus on mineralogic and biologic controls on the source and release of metals and acidity from mine-waste rock and hydrothermally altered areas. The second section describes a set of basin- to watershed-scale studies that not only investigate the source and release of metals and acidity but also the transport of these constituents away from the source areas. The third section is a summary of results from postremediation ecosystem monitoring. For more information on these and other project-related studies, please visit the project Web site at http://minerals.cr.usgs.gov/projects/contaminants/index.html. The Web site includes a complete bibliography and detailed descriptions of each interdisciplinary study.

Circular↗

USGS2010

Influence of sulfur-bearing polyatomic species on high precision measurements of Cu isotopic composition

An increased interest in high precision Cu isotope ratio measurements using multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) has developed recently for various natural geologic systems and environmental applications, these typically contain high concentrations of sulfur, particularly in the form of sulfate (SO 4 2- ) and sulfide (S). For example, Cu, Fe, and Zn concentrations in acid mine drainage (AMD) can range from 100??g/L to greater than 50mg/L with sulfur species concentrations reaching greater than 1000mg/L. Routine separation of Cu, Fe and Zn from AMD, Cu-sulfide minerals and other geological matrices usually incorporates single anion exchange resin column chromatography for metal separation. During chromatographic separation, variable breakthrough of SO 4 2- during anion exchange resin column chromatography into the Cu fractions was observed as a function of the initial sulfur to Cu ratio, column properties, and the sample matrix. SO 4 2- present in the Cu fraction can form a polyatomic 32 S- 14 N- 16 O- 1 H species causing a direct mass interference with 63 Cu and producing artificially light ?? 65 Cu values. Here we report the extent of the mass interference caused by SO 4 2- breakthrough when measuring ?? 65 Cu on natural samples and NIST SRM 976 Cu isotope spiked with SO 4 2- after both single anion column chromatography and double anion column chromatography. A set of five 100??g/L Cu SRM 976 samples spiked with 500mg/L SO 4 2- resulted in an average ?? 65 Cu of -3.50?????5.42??? following single anion column separation with variable SO 4 2- breakthrough but an average concentration of 770??g/L. Following double anion column separation, the average SO 4 2- concentration of 13??g/L resulted in better precision and accuracy for the measured ?? 65 Cu value of 0.01?????0.02??? relative to the expected 0??? for SRM 976. We conclude that attention to SO 4 2- breakthrough on sulfur-rich samples is necessary for accurate and precise measurements of ?? 65 Cu and may require the use of a double ion exchange column procedure. ?? 2010.

Chemical Geology↗

USGS2008

Progression in sulfur isotopic compositions from coal to fly ash: Examples from single-source combustion in Indiana

Sulfur occurs in multiple mineral forms in coals, and its fate in coal combustion is still not well understood. The sulfur isotopic composition of coal from two coal mines in Indiana and fly ash from two power plants that use these coals were studied using geological and geochemical methods. The two coal beds are Middle Pennsylvanian in age; one seam is the low-sulfur (< 1%) Danville Coal Member of the Dugger Formation and the other is the high-sulfur (> 5%) Springfield Coal Member of the Petersburg Formation. Both seams have ash contents of approximately 11%. Fly-ash samples were collected at various points in the ash-collection system in the two plants. The results show notable difference in ??34S for sulfur species within and between the low-sulfur and high-sulfur coal. The ??34S values for all sulfur species are exclusively positive in the low-sulfur Danville coal, whereas the ??34S values for sulfate, pyritic, and organic sulfur are both positive and negative in the high-sulfur Springfield coal. Each coal exhibits a distinct pattern of stratigraphic variation in sulfur isotopic composition. Overall, the ??34S for sulfur species values increase up the section in the low-sulfur Danville coal, whereas they show a decrease up the vertical section in the high-sulfur Springfield coal. Based on the evolution of ??34S for sulfur species, it is suggested that there was influence of seawater on peat swamp, with two marine incursions occurring during peat accumulation of the high-sulfur Springfield coal. Therefore, bacterial sulfate reduction played a key role in converting sulfate into hydrogen sulfide, sulfide minerals, and elemental sulfur. The differences in ??34S between sulfate sulfur and pyritic sulfur is very small between individual benches of both coals, implying that some oxidation occurred during deposition or postdeposition. The ??34S values for fly ash from the high-sulfur Springfield coal (averaging 9.7???) are greatly enriched in 34S relative to those in the parent coal (averaging 2.2???). This indicates a fractionation of sulfur isotopes during high-sulfur coal combustion. By contrast, the ??34S values for fly-ash samples from the low-sulfur Danville coal average 10.2???, only slightly enriched in 34S relative to those from the parent coal (average 7.5???). The ??34S values for bulk S determined directly from the fly-ash samples show close correspondence with the ??34S values for SO4- 2 leached from the fly ash in the low-sulfur coal, suggesting that the transition from pyrite to sulfate occurred via high-temperature oxidation during coal combustion. ?? 2007 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

USGS2009

Methods and basic data from mass-loading studies in American Fork, October 1999, and Mary Ellen Gulch, Utah, September 2000

Land-management agencies are faced with decisions about remediation in streams affected by mine drainage. In support of the U. S. Forest Service, for the Uinta National Forest, the U.S. Geological Survey conducted mass-loading studies in American Fork and Mary Ellen Gulch, Utah. Synoptic samples were collected along a 10,000-meter study reach in American Fork and 4,500-meter reach in Mary Ellen Gulch. Tracer-injection methods were combined with synoptic sampling methods to evaluate discharge and mass loading. This data-series report gives the results of the chemical analyses of these samples and provides the equations used to calculate discharge from tracer concentrations and loads from discharge and concentrations of the constituents. The detailed information from these studies will facilitate the preparation of interpretive reports and discussions with stakeholder groups. Data presented include detailed locations of the sampling sites, results of chemical analyses, and graphs of mass-loading profiles for major and trace elements in American Fork and Mary Ellen Gulch. Ultrafiltration was used to define filtered concentrations and total-recoverable concentrations were measured on unfiltered samples.

Utah↗

USGS2006

Navajo coal and air quality in Shiprock, New Mexico

Among the Navajo people, high levels of respiratory disease, such as asthma, exist in a population with low rates of cigarette smoking. Air quality outdoors and indoors affects respiratory health. Many Navajo Nation residents burn locally mined coal in their homes for heat, as coal is the most economical energy source. The U.S. Geological Survey and Dine College, in cooperation with the Navajo Division of Health, are conducting a study in the Shiprock, New Mexico, area to determine if indoor use of this coal might be contributing to some of the respiratory health problems experienced by the residents. Researchers in this study will (1) examine respiratory health data, (2) identify stove type and use, (3) analyze samples of coal that are used locally, and (4) measure and characterize air quality inside selected homes. This Fact Sheet summarizes the interim results of the study in both English and Navajo.

Fact Sheet↗

USGS2006

Navajo coal and air quality in Shiprock, New Mexico

Fact Sheet↗

USGS2000

Water-quality data for streams in the Boulder River Watershed, Jefferson County, Montana

Chemical data were collected in the Boulder River watershed of southwestern Montana during 1996-99 as part of a detailed interdisciplinary study characterizing the effects of historical inactive mines on streams in the watershed. This report presents water-quality data collected by the U.S. Geological Survey for physical properties, major ions, nutrients, and trace elements for 62 sites in and near the watershed. Supplementary historical water-quality data for 83 sites also are presented.

Montana↗

USGS2007

Regional geochemical results from the reanalysis of NURE stream sediment samples -- Eagle 3 degree quadrangle, east-central Alaska

This report presents reconnaissance geochemical data for a cooperative study in the Fortymile Mining District, east-central Alaska, initiated in 1997. This study has been funded by the U.S. Geological Survey (USGS) Mineral Resources Program. Cooperative funds were provided from various State of Alaska sources through the Alaska Department of Natural Resources. Results presented here represent the initial reconnaissance phase for this multidisciplinary cooperative study. In this phase, 239 sediment samples from the Eagle 3° Quadrangle of east-central Alaska, which had been collected and analyzed for the U.S. Department of Energy's National Uranium Resource Evaluation program (NURE) of the 1970's (Hoffman and Buttleman, 1996; Smith, 1997), are reanalyzed by newer analytical methods that are more sensitive, accurate, and precise (Arbogast, 1996; Taggart, 2002). The main objectives for the reanalysis of these samples were to establish lower limits of determination for some elements and to confirm the NURE data as a reliable predictive reconnaissance tool for future studies in Alaska's Eagle 3° Quadrangle. This study has wide implications for using the archived NURE samples and data throughout Alaska for future studies.

Alaska↗

USGS2025

Preparation and analysis methods for fish tissue collected from Lake Koocanusa, Montana

Lake Koocanusa, a reservoir, receives mine wastes from metallurgical coal mines in the Elk River Valley of British Columbia, Canada. Selenium and other elements discharged by the mines into the waters of the United States can pose unknown risks to aquatic life. The U.S. Geological Survey Wyoming-Montana Water Science Center can collaborate with Montana Fish, Wildlife and Parks and other State and Federal agencies to design studies and to collect fish tissues to help fill this knowledge gap. This report describes the processes, techniques, and methods used to collect and analyze fish tissue collected from Lake Koocanusa; and procedures used to review and manage data, including quality assurance and quality control procedures used by the U.S. Geological Survey Wyoming-Montana Water Science Center and supporting analytical laboratories. These fish tissue collections began in 2021.

Montana↗

USGS1971

Preliminary results of induced polarization-resistivity surveys in the Northgate district, Colorado

Induced polarization (I.P.) and resistivity surveys were made at selected locations in the Northgate district, Jackson County, Colorado. The objectives of the study were (1) to determine the feasibility of detecting and delineating pyrite-altered zones adjacent to fluorsparmineralized veins, and (2) to locate buried or obscured extensions of these fluorspar veins. The Northgate fluorspar deposits are among the largest in the western United States and have been commercially mined on a large scale since 1951. These deposits are being studied by Ronald G. Worl, U.S. Geological Survey, as part of an investigation of zoning in low-temperature barite, fluorite, and manganese oxide hydrothermal deposits. Of prime interest is the hypothesis that these deposits may form halos around adjacent base or precious metal deposits.

Colorado↗