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At least 829 records · Page 46Linked to original sources
USGS1986

Platinum-group element geochemistry of zoned ultramafic intrusive suites, Klamath Mountains, California and Oregon

Three postorogenic Alaskan-type ultramafic to mafic intrusive suites in the Klamath Mountains, ranging in age from 142 to 163 m.y. and intruding metavolcanic, metasedimentary, or ophiolitic cumulate ultramafie to gabbroic rocks, were examined for their platinum-group element content. The Lower Coon Mountain pluton consists of layered clinopyroxene-rich lithologies occurring in chronological sequence whereas the intrusive suite at Tincup Peak consists of a cogenetic sequence of wehrlite, clinopyroxenite, magnetite clinopyroxenite, feldspathic hornblende-magnetite clinopyroxenite, dunite-olivine clinopyroxenite, and hornblende gabbro. The ultramarie-mafic intrusive suite at Chanchelulla Peak, part of the Wildwood pluton, consists predominantly of clinopyroxenite, minor interlayered dunite, and wehrlite with minor hypabyssal gabbroic rocks. Clinopyroxene compositions in the three intrusive suites are calcium rich and range from Wo (sub 54.7) -En (sub 45.1) -Fs 19 to Wo (sub 44.9) -En (sub 43.8) -Fs (sub 11.3) and resemble clinopyroxene with alkalic affinities. Olivine ranges from Fo 72 to Fo 83 and plagioclase from An 68 to An 96 . Cyclic units of layered cumulus magnetite + spinel (+ or -ilmenite) and coarse interstitial magnetite occur at Tincup Peak and Lower Coon Mountain. All three intrusive suites contain disseminated pyrrhotite + chalcopyrite + or - pentlandite, but the Chanchelulla Peak intrusive body also contains lenticular zones of disseminated to interstitial sulfides near its contact with sulfide-bearing horn-felsic rocks. Characteristics of rocks from these three Klamath Mountains Alaskan-type intrusive suites are (1) Rh contents of near or less than 1 ppb, (2) Ir and Ru contents less than 100 and 20 ppb, (3) variable Pd contents between rock units within intrusive suites and among suites, and (4) relatively similar Pt contents within intrusive suites and among suites. Concentrations of Pd average 6.3 ppb at Lower Coon Mountain, 13.7 ppb at Chanchelulla Peak, and 36.4 ppb at Tincup Peak. Cohen-corrected abundance data for individual rock units within each intrusive suite yield a Pt/(Pt + Pd) ratio that is greater in olivine-rich rocks than in clinopy-roxenite than in gabbro suggesting chemical fractionation of Pd within intrusive suites.

Economic Geology↗
USGS2026

Complex carbonate ore mineralogy in the Mountain Pass carbonatite rare earth element deposit, USA

Economic concentrations of rare earth element (REE) minerals are uncommon in the Earth’s crust, with most occurring in carbonatites. Unlike most igneous rocks composed of silicate minerals, carbonatites are dominated by carbonate minerals, some of which can incorporate significant light REEs (LREEs; La, Ce, Pr, Nd). Technological applications of REEs are numerous and they have been identified as some of the most critical mineral commodities to the global economy. The Mountain Pass carbonatite stock in the Mojave Desert of California is the most economically significant REE deposit in the USA and contains a few to tens of percent (by volume) of the carbonate REE ore mineral bastnäsite. Despite the economic significance of the Mountain Pass deposit, studies of its ore mineralogy are limited. Here we present new carbonate ore mineralogy data for a compositionally diverse suite of carbonatitic rocks from the Mountain Pass stock and related dikes. Whole-rock geochemical data are integrated with mineral-scale textural and chemical data obtained by scanning electron microscopy (SEM), electron probe microanalysis (EPMA), and microRaman spectroscopy. Our results document a complex spectrum of REE-bearing carbonate minerals and intermediate mixed-layer structures. Mineral species include bastnäsite [REE(CO 3 )F], hydroxylbastnäsite [REE(CO 3 )OH], parisite [Ca(REE) 2 (CO 3 ) 3 F 2 ], synchysite [Ca(REE)(CO 3 ) 2 F], röntgenite [Ca 2 (Ce,La) 3 (CO 3 ) 5 F 3 ], and sahamalite [(Mg,Fe 2+ )(REE) 2 (CO 3 ) 4 ]. Carbonate ore mineralogy is heterogeneous within and between samples, including at the intracrystal scale. Complexly zoned crystals exhibit as many as five to six different compositional domains and syntaxial intergrowths, commonly with the more Ca-rich varieties (parisite, synchysite) forming crystal rims that surround relict bastnäsite cores. We attribute the phenocryst variability to changes in the chemistry and temperature of primary carbonatite magmas and evolved/exsolved fluids. Cross-cutting vein textures of calcite, celestine and various REE carbonate minerals, interstitial bastnäsite crystallization, breccia blocks lined by fine-grained bastnäsite, and the presence of hydroxylbastnäsite and partially hydroxylated bastnäsite point to the role of secondary hydrothermal processes in REE mineralization. Fluorcarbonate mineral compositions demonstrate that La and Ce are more structurally abundant in bastnäsite, whereas the more Ca-rich species (parisite, synchysite) contain a greater proportion of REE heavier than Pr (Nd, Sm, Eu, Gd) and Y. Atomic ratios of Pr/(Nd + Pr) are likewise variable, with the highest average value for bastnäsite (0.25) compared to parisite (0.22) and sychysite (0.21). This finding has geometallurgical implications, given that current mining operations are focused on recovery of Nd and Pr for high field strength permanent magnets and the Nd/Pr ratios are a critical factor in ore processing and magnet manufacture.

California↗
USGS2025

Rare earth element-mineralized carbonatite in the Bear Lodge Alkaline Complex, USA—Ore genesis implications from fluid inclusion characterization

Rare earth element (REE) resources of the Bear Lodge Alkaline Complex, Wyoming, are hosted in variably leached carbonatite spatially related to diatreme breccia pipes. We investigated the genesis of REE and lesser-known gold resources through fluid inclusion analysis of carbonatite, fluorite breccia, and smoky quartz vein samples. Physicochemical characteristics of inclusion-trapped fluids were evaluated using petrography, microthermometry, Raman spectroscopy, decrepitate mound analysis, energy-dispersive spectroscopy, laser ablation inductively coupled plasma mass spectrometry, and noble gas isotope analysis. Microthermometry results reveal three fluid types that affected carbonatite dikes within deeper zones that escaped near-surface, ore-grade REE enrichment: (1) high-temperature (330–432°C) magmatic fluid captured in fine-grained calcite; (2) REE-enriched alkali bicarbonate-sulfate brine; and (3) low-temperature (117–182°C) diluted magmatic or meteoric water. Multiphase brine-like inclusions contain burbankite, nahcolite, strontianite, celestine and alkali sulfate daughter crystals, linking them to early burbankite mineralization. Peripheral smoky quartz and fluorite occurrences at Smith Ridge, 1.5 km from the central carbonatite dike swarm, contain primary inclusions that are Cl-poor and rich in Na-HCO 3 -SO 4 , similar to secondary and pseudosecondary inclusions in carbonatites. Helium isotopes reveal a MORB-like source for carbonatite samples and an older crust signature at Smith Ridge, consistent with the proximal ridge-top exposures of Archean granite. Results from this fluid inclusion study coupled with previous studies of carbonatite mineral paragenesis, show that light REEs (LREEs) were not mobilized great distances. Instead, burbankite crystallized within carbonatite from alkali bicarbonate fluids. With sodium retained in early burbankite, outward-emanating fluids enriched in potassium relative to sodium (higher K:Na) resulted in potassium–ferric iron metasomatism of silicate host rocks. This alkali fractionation was accompanied by fractionation of LREEs and heavy REEs (HREEs), with LREEs dominating the central carbonatite resources. In contrast, areas of peripheral REE mineralization at Bear Lodge are commonly characterized by higher HREE:LREE ratios. The K:Na ratio of associated fenites or alteration assemblages could be indicative of early crystallized burbankite in carbonatites and REE fractionation processes potentially leading to areas of concentrated HREEs with greater supply vulnerabilities.

South Dakota, Wyoming↗
USGS2012

Origin of an unusual monazite-xenotime gneiss, Hudson Highlands, New York: SHRIMP U-Pb geochronology and trace element geochemistry

A pod of monazite-xenotime gneiss (MXG) occurs within Mesoproterozoic paragneiss, Hudson Highlands, New York. This outcrop also contains granite of the Crystal Lake pluton, which migmatized the paragneiss. Previously, monazite, xenotime, and zircon from MXG, plus detrital zircon from the paragneiss, and igneous zircon from the granite, were dated using multi-grain thermal ionization mass spectrometry (TIMS). New SEM imagery of dated samples reveals that all minerals contain cores and rims. Thus TIMS analyses comprise mixtures of age components and are geologically meaningless. New spot analyses by sensitive high resolution ion microprobe (SHRIMP) of small homogeneous areas on individual grains allows deconvolution of ages within complexly zoned grains. Xenotime cores from MXG formed during two episodes (1034 ± 10 and 1014 ± 3 Ma), whereas three episodes of rim formation are recorded (999 ± 7, 961 ± 11, and 874 ± 11 Ma). Monazite cores from MXG mostly formed at 1004 ± 4 Ma; rims formed at 994 ± 4, 913 ± 7, and 890 ± 7 Ma. Zircon from MXG is composed of oscillatory-zoned detrital cores (2000-1170 Ma), plus metamorphic rims (1008 ± 7, 985 ± 5, and ∼950 Ma). In addition, MXG contains an unusual zircon population composed of irregularly-zoned elongate cores dated at 1036 ± 5 Ma, considered to be the time of formation of MXG. The time of granite emplacement is dated by oscillatory-zoned igneous cores at 1058 ± 4 Ma, which provides a minimum age constraint for the time of deposition of the paragneiss. Selected trace elements, including all REE plus U and Th, provide geochemical evidence for the origin of MXG. MREE-enriched xenotime from MXG are dissimilar from typical HREE-enriched patterns of igneous xenotime. The presence of large negative Eu anomalies and high U and Th in monazite and xenotime are uncharacteristic of typical ore-forming hydrothermal processes. We conclude that MXG is the result of unusual metasomatic processes during high grade metamorphism that was initiated at about 1035 Ma. This rock was then subjected to repeated episodes of dissolution/reprecipitation for about 150 m.y. during regional cooling of the Hudson Highlands.

New York↗
USGS1998

Lead poisoning and trace elements in common eiders Somateria mollissima from Finland

We collected carcasses of 52 common eider Somateria mollissima adults and ducklings and blood samples from 11 nesting eider hens in the Gulf of Finland near Helsinki in 1994, 1995 and 1996. Samples of liver tissue were analysed for arsenic, cadmium, chromium, copper, iron, lead, magnesium, manganese, mercury, molybdenum, selenium and zinc. Blood was analysed for lead, mercury and selenium. Most of the 21 adults examined at necropsy were emaciated with empty gizzards, and no ingested shotgun pellets or other metal were found in any of the birds. Three adult females had a combination of lesions and tissue lead residues characteristic of lead poisoning. Two of these birds had acid-fast intranuclear inclusion bodies in renal epithelial cells and high concentrations of lead (73.4 and 73.3 ppm; all liver residues reported on dry weight basis) in their livers. The third was emaciated with a liver lead concentration of 47.9 ppm. An adult male had a liver lead concentration of 81.7 ppm, which is consistent with severe clinical poisoning. Two other adults, one male and one female, had liver lead concentrations of 14.2 and 8.03 ppm, respectively. Lead concentrations in the blood of hens ranged from 0.11 to 0.63 ppm wet weight. Selenium residues of A?60 ppm were found in the livers of five adult males. Selenium concentrations in the blood of hens ranged from 1.18 to 3.39 ppm wet weight. Arsenic concentrations of 27.5-38.5 ppm were detected in the livers of four adult females. Detectable concentrations of selenium, mercury and molybdenum were found more frequently in the livers of adult males arriving on the breeding grounds than in incubating females, while the reverse was true for arsenic, lead and chromium. Mean concentrations of selenium, copper and molybdenum were higher in the livers of arriving males than in the livers of incubating hens, but hens had greater concentrations of iron and magnesium. Concentrations of trace elements were lower in the livers of ducklings than in the livers of adults.

Wildlife Biology↗
USGS2000

Lateral ramps in the folded Appalachians and in overthrust belts worldwide— A fundamental element of thrust-belt architecture

Lateral ramps are zones where decollements change stratigraphic level along strike; they differ from frontal ramps, which are zones where decollements change stratigraphic level perpendicular to strike. In the Appalachian Mountains, the surface criteria for recognizing the subsurface presence of lateral ramps include (1) an abrupt change in wavelength or a termination of folds along strike, (2) a conspicuous change in the frequency of mapped faults or disturbed zones (extremely disrupted duplexes) at the surface, (3) long, straight river trends emerging onto the coastal plain or into the Appalachian Plateaus province, (4) major geomorphic discontinuities in the trend of the Blue Ridge province, (5) interruption of Mesozoic basins by cross-strike border faults, and (6) zones of modern and probable ancient seismic activity. Additional features related to lateral ramps include tectonic windows, cross-strike igneous intrusions, areas of giant landslides, and abrupt changes in Paleozoic sedimentation along strike. Proprietary strike-line seismic-reflection profiles cross three of the lateral ramps that were identified by using the surface criteria. The profiles confirm their presence and show their detailed nature in the subsurface. Like frontal ramps, lateral ramps are one of two possible consequences of fold-and-thrust-belt tectonics and are common elements in the Appalachian fold-and-thrust belt. A survey of other thrust belts in the United States and elsewhere strongly suggests that lateral ramps at depth can be identified by their surface effects. Lateral ramps probably are the result of thrust sheet motion caused by continued activation of ancient cratonic fracture systems. Such fractures localized the transform faults along which the continental segments adjusted during episodes of sea-floor spreading.

Pennsylvania↗
USGS1994

Major ions, nutrients, and trace elements in the Mississippi River near Thebes, Illinois, July through September 1993

Extensive flooding in the upper Mississippi River Basin during summer 1993 had a significant effect on the water quality of the Mississippi River. To evaluate the change in temporal distribution and transport of dissolved constituents in the Mississippi River, six water samples were collected by a discharge-weighted method from July through September 1993 near Thebes, Illinois. Sampling at this location provided water-quality information from the upper Mississippi, the Missouri, and the Illinois River Basins. Dissolved major constituents that were analyzed in each of the samples included bicarbonate, calcium (Ca), carbonate (C03), chloride (Cl), dissolved organic carbon, magnesium (Mg), potassium (K), silica NOD, sodium (Na), and sulfate (S04). Dissolved nutrients included ammonium ion (NH4), nitrate (N03), nitrite (N02), and orthophosphate (P04) . Dissolved trace elements included aluminum (Al), arsenic (As), barium (Ba), boron (B), beryllium (Be), bromide (Br), cadmium (Cd), chromium (Cr), cobalt, (Co), copper (Cu), fluoride (F), iron (Fe), lead, lithium (Li), manganese (Mn), mercury (Hg), molybdenum (Mo), nickel (Ni), strontium (Sr), thallium, uranium (U), vanadium (V), and zinc (Zn). Other physical properties of water that were measured included specific conductance, pH and suspended-sediment concentration (particle size, less than 63 micrometers). Results of this study indicated that large quantities of dissolved constituents were transported through the river system. Generally, pH, alkalinity, and specific conductance and the concentrations of B, Br, Ca, Cl, Cr, K, Li, Mg, Mo, Na, S04, Sr, U, and V increased as water discharge decreased, while concentrations of F, Hg, and suspended sediment sharply decreased as water discharge decreased after the crest of the flood. Concentrations of other constituents, such as Al, As, Ba, Be, Co, Cu, Ni, N03, N02, NH4, P04, and Si02, varied with time as discharge decreased after the crest of the flood. For most constituents, the load transported during floods generally is much greater than that transported during low-flow conditions. How ever, for Cd, Cr, Fe, Mn, V, and Zn, loads increased substantially as water discharge decreased after the crest of the flood.

Illinois↗
USGS1997

Trace elements and organic compounds associated with riverbed sediments in the Rio Grande/Rio Bravo basin, Mexico and Texas

In 1991, the Texas Natural Resource Conservation Commission (TNRCC) was mandated by the Texas Clean Rivers Act (Senate Bill 818) to assess water quality of rivers in Texas. Recent efforts to collect information for the assessment of water quality in the Rio Grande/Rio Bravo Basin have involved Federal agencies on both sides of the 1,248-mile U.S.-Mexico border?U.S. Environmental Protection Agency, U.S. Geological Survey (USGS), Secretaria de Desarollo Social (Secretary for Social Development, Mexico), National Water Commission of Mexico, and International Boundary and Water Commission?as well as State and local agencies in a spirit of international cooperation. Substantial efforts have been made to gather data needed to determine the quality of water and ecological status of the Rio Grande/Rio Bravo, especially at sites along the border (fig. 1). The purpose of this report is to assess selected historical data of trace elements and organic compounds in riverbed sediments of the Rio Grande/Rio Bravo, and of the Pecos River and the Arroyo Colorado in Texas.

Fact Sheet↗
USGS2014

Platinum-group elements: So many excellent properties

The platinum-group elements (PGE) include platinum, palladium, rhodium, ruthenium, iridium, and osmium. These metals have similar physical and chemical properties and occur together in nature. The properties of PGE, such as high melting points, corrosion resistance, and catalytic qualities, make them indispensable to many industrial applications. PGE are strategic and critical materials for many nations because they are essential for important industrial applications but are mined in a limited number of places and have no adequate substitutes. Exploration and mining companies have found approximately 104,000 metric tons of PGE (with minor gold) in mineral deposits around the world that could be developed. For PGE, almost all known production and resources are associated with three geologic features: the Bushveld Complex, a layered mafic-to-ultramafic intrusion in South Africa; the Great Dyke, a layered mafic-to-ultramafic intrusion in Zimbabwe; and sill-like intrusions associated with flood basalts in the Noril’sk-Talnakh area, Russia. To help predict where PGE supplies might be located, USGS scientists study how and where PGE resources are concentrated in the Earth's crust and use that knowledge to assess the likelihood that undiscovered PGE deposits may exist. Techniques used for assessing mineral resources were developed by the USGS to support the stewardship of Federal lands and evaluate mineral resource availability in a global context. The USGS also compiles statistics and information on the worldwide supply, demand, and flow of PGE. These data are all used to inform U.S. national policymakers.

Fact Sheet↗
USGS2014

The rare-earth elements: Vital to modern technologies and lifestyles

Until recently, the rare-earth elements (REEs) were familiar to a relatively small number of people, such as chemists, geologists, specialized materials scientists, and engineers. In the 21st century, the REEs have gained visibility through many media outlets because of (1) the public has recognized the critical, specialized properties that REEs contribute to modern technology, as well as (2) China's dominance in production and supply of the REEs and (3) international dependence on China for the majority of the world's REE supply. Since the late 1990s, China has provided 85–95 percent of the world’s REEs. In 2010, China announced their intention to reduce REE exports. During this timeframe, REE use increased substantially. REEs are used as components in high technology devices, including smart phones, digital cameras, computer hard disks, fluorescent and light-emitting-diode (LED) lights, flat screen televisions, computer monitors, and electronic displays. Large quantities of some REEs are used in clean energy and defense technologies. Because of the many important uses of REEs, nations dependent on new technologies, such as Japan, the United States, and members of the European Union, reacted with great concern to China’s intent to reduce its REE exports. Consequently, exploration activities intent on discovering economic deposits of REEs and bringing them into production have increased.

Fact Sheet↗
USGS2018

Rare earth element and rare metal inventory of central Asia

Rare earth elements (REE), with their unique physical and chemical properties, are an essential part of modern living. REE have enabled development and manufacture of high-performance materials, processes, and electronic technologies commonly used today in computing and communications, clean energy and transportation, medical treatment and health care, glass and ceramics, aerospace and defense, and metallurgy and chemical refining. Central Asia is an emerging REE and rare metals (RM) producing region. A newly compiled inventory of REE-RM-bearing mineral occurrences and delineation of areas-of-interest indicate this region may have considerable undiscovered resources.

Fact Sheet↗
USGS2024

Balancing natural resource use and extraction of uranium and other elements in the Grand Canyon region

The Grand Canyon region is an important natural, cultural, and archeological resource known worldwide. The region contains uranium resources that could be used to generate electricity. The U.S. Geological Survey (USGS), in cooperation with the National Park Service, Bureau of Land Management, and U.S. Department of Agriculture Forest Service, is conducting studies to answer questions about the environmental effects of mining uranium and other associated elements in the region.

Arizona↗
USGS2025

Rare earth elements on the Moon

Rare earth elements (REEs) are a scarce but vital resource for our modern economies and lifestyles. Since the late 1990s, China has supplied the vast majority of the world’s refined REEs. Increasing global demand has broadened the search for REE deposits to unconventional places, including the Moon. Although most lunar rocks have very low REE concentrations, Apollo samples showed that one type of lunar rock containing potassium (K), REEs, and phosphorus (P)—known by the acronym KREEP—has high concentrations of REEs. Data from orbiting satellites have identified locations where substantial deposits of KREEP are likely. The viability of mining these deposits depends on the evolution of REE economics, the development of the Earth-Moon infrastructure, and the findings from future lunar mineral exploration missions.

Fact Sheet↗
USGS1985

Maps showing distribution of anomalous concentrations of trace elements in the magnetic fraction of heavy-mineral concentrates, Domeland Wilderness and contiguous roadless areas, Kern and Tulare counties, California

The purpose of this map is to provide a geochemical framework for the mineral resource assessment of the Domeland Wilderness and contiguous roadless areas. The map shows the distribution of anomalous elements in the magnetic fraction of heavy-mineral concentrates derived from stream sediments.

California↗
USGS1993

Mineral resource assessment of rare-earth elements, thorium, titanium, and uranium in the Greenville 1° x 2° quadrangle, South Carolina, Georgia, and North Carolina

Mineral resources of the Greenville 1° x 2° quadrangle, South Carolina, Georgia, and North Carolina, were assessed between 1984 and 1990 under the Conterminuous United States Mineral Assessment Program (CUSMAP) of the U.S. Geological Survey (USGS). The mineral resource assessments were made on the basis of geologic, geochemical, and geophysical investigations and the presence of mines, prospects, and mineral occurrences from the literature. This report is an assessment of the rare-earth elements (REE), thorium, titanium, and uranium resources in the Greenville quadrangle and is based on heavy mineral concentrates collected in 1951-54 by the USGS (Overstreet and others, 1968; Caldwell and White, 1973; Cuppels and White, 1973); on the results of the U.S. Department of Energy, National Uranium Resource Evaluation (NURE) sampling program (Ferguson, 1978, 1979); on analyses of stream-sediment and heavy-mineral-concentrate samples (Jackson and Moore, 1992, G.C Cullin, USGS, unpub. data, 1992) on maps showing aerial gamma radiation in the Greenville quadrangle (D.L. Daniels, USGS, unpub. data, 1992); and on the geology as mapped by Nelson and others (1987, 1989).

Georgia, North Carolina, South Carolina↗
USGS2000

Distribution of a suite of elements including arsenic and mercury in Alabama coal

Arsenic and other elements are unusually abundant in Alabama coal. This conclusion is based on chemical analyses of coal in the U.S. Geological Survey's National Coal Resources Data System (NCRDS; Bragg and others, 1994). According to NCRDS data, the average concentration of arsenic in Alabama coal (72 ppm) is three times higher than is the average for all U.S. coal (24 ppm). Of the U.S. coal analyses for arsenic that are at least 3 standard deviations above the mean, approximately 90% are from the coal fields of Alabama. Figure 1 contrasts the abundance of arsenic in coal of the Warrior field of Alabama (histogram C) with that of coal of the Powder River Basin, Wyoming (histogram A), and the Eastern Interior Province including the Illinois Basin and nearby areas (histogram B). The Warrior field is by far the largest in Alabama. On the histogram, the large 'tail' of very high values (> 200 ppm) in the Warrior coal contrasts with the other two regions that have very few analyses greater than 200 ppm.

Alabama↗
USGS2002

Whole-rock and glass major-element geochemistry of Kilauea Volcano, Hawaii, near-vent eruptive products: September 1994 through September 2001

This report presents major-element geochemical data for glasses and whole-rock aliquots among 523 lava samples collected near the vent on Kilauea's east rift zone between September 1994 and October 2001. Information on sample collection, analysis techniques and analytical standard reproducibility are presented as a PDF file, which also includes a detailed explantion of the categories of sample information presented in the database spreadsheet. The sample database is downloadable as a separate Microsoft Excel file.

Hawai'i↗