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At least 1,189 records · Page 66Linked to original sources
USGS1999

Data on Holocene tephra (volcanic ash) deposits in the Alaska Peninsula and lower Cook Inlet region of the Aleutian volcanic arc, Alaska

This site provides information about the number, thickness, and grainsize of Holocene volcanic ash deposits at 50 localities in the eastern Aleutian volcanic arc. In addition, the major-element compositions of the glasses separated from more than 350 samples of tephra from these localities, determined by electron microprobe, are presented as a basis for correlating samples. Where known with reasonable certainty, the source of an analyzed sample is also identified for use in comparative studies of magma chemistry.

Alaska↗
USGS1979

Thermoluminescence dating of Hawaiian basalt

The thermoluminescence (TL) properties of plagioclase separates from 11 independently dated alkalic basalts 4,500 years to 3.3 million years old and 17 tholeiitic basalts 16 years to 450,000 years old from the Hawaiian Islands were investigated for the purpose of developing a TL dating method for young volcanic rocks. Ratios of natural to artificial TL intensity, when normalized for natural radiation dose rates, were used to quantify the thermoluminescence response of individual samples for age-determination purposes. The TL ratios for the alkalic basalt plagioclase were found to increase with age at a predictable exponential rate that permits the use of the equation for the best-fit line through a plot of the TL ratios relative to known age as a TL age equation. The equation is applicable to rocks ranging in composition from basaltic andesite to trachyte over the age range from about 2,000 to at least 250,000 years before present (B.P.). The TL ages for samples older than 50,000 years have a calculated precision of less than :t 10 percent and a potential estimated accuracy relative to potassium-argon ages of approximately :t 10 percent. An attempt to develop a similar dating curve for the tholeiitic basalts was not as successful, primarily because the dose rates are on the average lower than those for the alkalic basalts by a factor of 6, resulting in lower TL intensities in the tholeiitic basalts for samples of equivalent age, and also because the age distribution of dated material is inadequate. The basic TL properties of the plagioclase from the two rock types are similar, however, and TL dating of tholeiitic basalts should eventually be feasible over the age range 10,000 to at least 200,000 years B.P. The average composition of the plagioclase separates from the alkalic basalts ranges from oligoclase to andesine; compositional variations within this range have no apparent effect on the TL ratios. The average composition of the plagioclase from the tholeiitic basalts is labradorite. The natural radiogenic dose rates for the alkalic basalts calculated on the basis of assumed secular equilibrium range from 0.228 to 0.462 rad per year and average 0.335 rad per year exclusive of the cosmic-ray energy dose and with the alpha-particle component equal to one-tenth of the total alpha decay energy. The TL measurements were made using material of a 37 to 44-micrometer size range; the crushing required during sample preparation was found to have a negligible effect on natural TL. Both natural and artificial TL were filtered to the bandwidth 3,500 A to 5,000 A to restrict the light detected to that from the plagioclase emission peak centered at about 4,500 A and associated with structural defects. Within this bandwidth, the natural TL from both the alkalic and tholeiitic basalt plagioclase consists of a single peak with a maximum amplitude at about 350?C; the artificial TL glow curves produced by an exposure of the drained samples to a standard dose of X-radiation consist of four broad, variably overlapping peaks with maxima at about 110?C, 150?C, 225?C, and 300?C. The maximum amplitude of the 350?C natural and 300?C artificial TL peaks, both produced by the same general activation energy distribution of trapping centers, were used for TL dating. The high-temperature artificial TL peak occurs at a lower temperature than the corresponding natural TL peak owing to the presence of a large number of electrons retained in traps near the lower end of the trap-depth energy range in samples whose TL is measured a short time after intense artificial irradiation. These traps remain essentially empty in the natural environment owing to spontaneous decay and do not produce measurable low-temperature natural TL peaks. With prolonged storage after irradiation, the 300?C artificial TL peak migrates to higher temperatures and decreases in amplitude.

Professional Paper↗
USGS1980

Crystals of coexisting alunite and jarosite, Goldfield, Nevada

Alunite (KAl 3 (SO 4 ) 2 (OH) 6 ) and jarosite (KFe 3 (SO 4 ) 2 (OH) 6 ) coexist in optically continuous crystals in a sample from the Goldfield mining district, Esmeralda County, Nev. Beam scans with an electron microprobe indicate that no intermediate minerals of the solid-solution series alunite-jarosite occur in these crystals. An Eh-pH diagram demonstrating the equilibrium relations between alunite, jarosite, and geothite suggests the crystals most likely developed by a rise in Eh, which oxidized ferrous to ferric iron, thus allowing jarosite to precipitate.

Nevada↗
USGS2002

The Effect of Selected Cleaning Techniques on Berkshire Lee Marble: A Scientific Study at Philadelphia City Hall

This report describes a scientific investigation of the effects of eight different cleaning techniques on the Berkshire Lee marble component of the facade of the East Center Pavilion at Philadelphia City Hall; the study was commissioned by the city of Philadelphia. The eight cleaning techniques evaluated in this study were power wash (proprietary gel detergent followed by water rinse under pressure), misting (treatment with potable, nebulized water for 24-36 hours), gommage (proprietary Thomann-Hanry low-pressure, air-driven, small-particle, dry abrasion), combination (gommage followed by misting), Armax (sodium bicarbonate delivered under pressure in a water wash), JOS (dolomite powder delivered in a low-pressure, rotary-vortex water wash), laser (thermal ablation), and dry ice (powdered-dry-ice abrasion delivered under pressure). In our study approximately 160 cores were removed from the building for laboratory analysis. We developed a computer program to analyze scanning-electron-micrograph images for the microscale surface roughness and other morphologic parameters of the stone surface, including the near-surface fracture density of the stone. An analysis of more than 1,100 samples cut from the cores provided a statistical basis for crafting the essential elements of a reduced-form, mixed-kinetics conceptual model that represents the deterioration of calcareous stone in terms of self-organized soiling and erosion patterns. This model, in turn, provided a basis for identifying the variables that are affected by the cleaning techniques and for evaluating the extent to which such variables influence the stability of the stone. The model recognizes three classes of variables that may influence the soiling load on the stone, including such exogenous environmental variables as airborne moisture, pollutant concentrations, and local aerodynamics, and such endogenous stone variables as surface chemistry and microstructure (fracturing, roughness, and so on). This study showed that morphologic variables on the mesoscale to macroscale are not generally affected by the choice of a cleaning technique. The long-term soiling pattern on the building is independent of the cleaning technique applied. This study also showed that soluble salts do not play a significant role in the deterioration of Berkshire Lee marble. Although salts were evident in cracks and fissures of the heavily soiled stone, such salts did not penetrate the surface to a depth of more than a few hundred micrometers. The criteria used to differentiate the cleaning techniques were ultimately based on the ability of each technique to remove soiling without altering the texture of the stone surface. This study identified both the gommage and JOS techniques as appropriate for cleaning ashlar surfaces and the combination technique as appropriate for cleaning highly carved surfaces at the entablatures, cornices, and column capitals.

Professional Paper↗
USGS2003

Computation and analysis of the instantaneous-discharge record for the Colorado River at Lees Ferry, Arizona — May 8, 1921, through September 30, 2000

A gaging station has been operated by the U.S. Geological Survey at Lees Ferry, Arizona, since May 8, 1921. In March 1963, Glen Canyon Dam was closed 15.5 miles upstream, cutting off the upstream sediment supply and regulating the discharge of the Colorado River at Lees Ferry for the first time in history. To evaluate the pre-dam variability in the hydrology of the Colorado River, and to determine the effect of the operation of Glen Canyon Dam on the downstream hydrology of the river, a continuous record of the instantaneous discharge of the river at Lees Ferry was constructed and analyzed for the entire period of record between May 8, 1921, and September 30, 2000. This effort involved retrieval from the Federal Records Centers and then synthesis of all the raw historical data collected by the U.S. Geological Survey at Lees Ferry. As part of this process, the peak discharges of the two largest historical floods at Lees Ferry, the 1884 and 1921 floods, were reanalyzed and recomputed. This reanalysis indicates that the peak discharge of the 1884 flood was 210,000±30,000 cubic feet per second (ft 3 /s), and the peak discharge of the 1921 flood was 170,000±20,000 ft 3 /s. These values are indistinguishable from the peak discharges of these floods originally estimated or published by the U.S. Geological Survey, but are substantially less than the currently accepted peak discharges of these floods. The entire continuous record of instantaneous discharge of the Colorado River at Lees Ferry can now be requested from the U.S. Geological Survey Grand Canyon Monitoring and Research Center, Flagstaff, Arizona, and is also available electronically at http://www.gcmrc.gov. This record is perhaps the longest (almost 80 years) high-resolution (mostly 15- to 30-minute precision) times series of river discharge available. Analyses of these data, therefore, provide an unparalleled characterization of both the natural variability in the discharge of a river and the effects of dam operations on a river. Following the construction and quality-control checks of the continuous record of instantaneous discharge, analyses of flow duration, sub-daily flow variability, and flood frequency were conducted on the pre- and post-dam parts of the record. These analyses indicate that although the discharge of the Colorado River varied substantially prior to the closure of Glen Canyon Dam in 1963, operation of the dam has caused changes in discharge that are more extreme than the pre-dam natural variability. Operation of the dam has eliminated flood flows and base flows, and thereby has effectively "flattened" the annual hydrograph. Prior to closure of the dam, the discharge of the Colorado River at Lees Ferry was lower than 7,980 ft 3 /s half of the time. Discharges lower than about 9,000 ft 3 /s were important for the seasonal accumulation and storage of sand in the pre-dam river downstream from Lees Ferry. The current operating plan for Glen Canyon Dam no longer allows sustained discharges lower than 8,000 ft 3 /s to be released. Thus, closure of the dam has not only cut off the upstream supply of sediment, but operation of the dam has also largely eliminated discharges during which sand could be demonstrated to accumulate in the river. In addition to radically changing the hydrology of the river, operation of the dam for hydroelectric-power generation has introduced large daily fluctuations in discharge. During the pre-dam era, the median daily range in discharge was only 542 ft 3 /s, although daily ranges in discharge exceeding 20,000 ft 3 /s were observed during the summer thunderstorm season. Relative to the pre-dam period of record, dam operations have increased the daily range in discharge during all but 0.1 percent of all days. The post-dam median daily range in discharge, 8,580 ft 3 /s, exceeds the pre-dam median discharge of 7,980 ft 3 /s. Operation of the dam has also radically changed the frequency of floods on the Colorado River at Lees Ferry. The frequency of floods with peak discharges larger than about 29,000 ft 3 /s has greatly decreased, while the frequency of smaller floods, with peak discharges between 18,500 and 29,000 ft 3 /s, has increased substantially. Operation of the dam has greatly extended the duration of smaller floods; for example, each of the four longest periods of sustained flows in excess of 18,500 ft 3 /s occurred after closure of the dam.

Arizona↗
USGS2008

Analysis of GPS-measured deformation associated with the 2004-2006 dome-building eruption of Mount St. Helens, Washington

Detecting far-field deformation at Mount St. Helens since the crater-forming landslide and blast in 1980 has been difficult despite frequent volcanic activity and improved monitoring techniques. Between 1982 and 1991, the systematic extension of line lengths in a regional GPS trilateration network is consistent with recharge of a deep magma chamber during that interval. The rate of extension, however, averages only 3 mm/yr, and some of this apparent deformation may result from systematic scale error in the electronic distance measurements. Subsequent GPS surveys and data from a continuous GPS station, located 9 km north of Mount St. Helens and operating since 1997, show no significant volcanic deformation until the start of unrest on September 23, 2004. The current eruption has been accompanied by subtle but widespread inward and downward movement of GPS monitoring stations, exponentially decreasing with time and totaling as much as 30 mm. The observed deformation is consistent with the predictions of an elastic half-space model of a vertically elongate magma chamber with its center at a depth of around 7 to 8 km and with a total cavity-volume loss of about 16–24×10 6 m 3 . The discrepancy between the estimated cavity-volume loss and the >83×10 6 -m 3 volume of the erupted dome can be explained, for the most part, by exsolution of gas in the stored magma and by minor input of new magma during the eruption.

Washington↗
USGS2008

Plagioclase populations and zoning in dacite of the 2004-2005 Mount St. Helens eruption: Constraints for magma origin and dynamics

We investigated plagioclase phenocrysts in dacite of the 2004-5 eruption of Mount St. Helens to gain insights into the magmatic processes of the current eruption, which is characterized by prolonged, nearly solid-state extrusion, low gas emission, and shallow seismicity. In addition, we investigated plagioclase of 1980-86 dacite. Light and Nomarski microscopy were used to texturally characterize plagioclase crystals. Electron microprobe analyses measured their compositions. We systematically mapped and categorized all plagioclase phenocrysts in a preselected area according to the following criteria: (1) occurrence of zones of acicular orthopyroxene inclusions, (2) presence of dissolution surface(s), and (3) spatial association of 1 and 2. Phenocrysts fall into three main categories; one category contains four subcategories. The range of anorthite (An) content in 2004-5 plagioclase is about An 57-35 during the last 30-40 percent crystallization of plagioclase phenocrysts. Select microphenocrysts (10-50 μm) range from An 30 to An 42 . Anorthite content is lowest near outermost rims of phenocrysts, but zonation patterns between interior and rim indicate variable trends that correlate with textural features. Crystals without dissolution surfaces (about 14 percent of total) show steadily decreasing An content outward to the crystal rim (outer ~80 μm). All other crystals are banded as a consequence of dissolution; dissolution surfaces are band boundaries. Such crystals display normal outward An zoning within a single band that, following dissolution, is then overgrown abruptly by high-An material of the next band. Swarms of acicular orthopyroxene inclusions in plagioclase are characteristic of 2004-5 dacite. They occur mostly inward of dissolution surfaces, where band composition reaches lowest An content. The relative proportions of the three crystal types are distinctly different between 2004-5 dacite and 1980s dome dacite. We propose that crystals with no dissolution surfaces are those that were supplied last to the shallow reservoir, whereas plagioclase with increasingly more complex zoning patterns (that is, the number of zoned bands bounded by dissolution surfaces) result from prolonged residency and evolution in the reservoir. We propose that banding and An zoning across multiple bands are primarily a response to thermally induced fluctuations in crystallinity of the magma in combination with recharge; a lesser role is ascribed to cycling crystals through pressure gradients. Crystals without dissolution surfaces, in contrast, could have grown only in response to steady(?) decompression. Some heating-cooling cycles probably postdate the final eruption in 1986. They resulted from small recharge events that supplied new crystals that then experienced resorption-growth cycles. We suggest that magmatic events shortly prior to the current eruption, recorded in the outermost zones of plagioclase phenocrysts, began with the incorporation of acicular orthopyroxene, followed by last resorption, and concluded with crystallization of euhedral rims. Finally, we propose that 2004-5 dacite is composed mostly of dacite magma that remained after 1986 and underwent subsequent magmatic evolution but, more importantly, contains a component of new dacite from deeper in the magmatic system, which may have triggered the new eruption.

Washington↗
USGS2014

Petrologic insights into basaltic volcanism at historically active Hawaiian volcanoes

Study of the petrology of Hawaiian volcanoes, in particular the historically active volcanoes on the Island of Hawai‘i, has long been of worldwide scientific interest. When Dr. Thomas A. Jaggar, Jr., established the Hawaiian Volcano Observatory (HVO) in 1912, detailed observations on basaltic activity at Kīlauea and Mauna Loa volcanoes increased dramatically. The period from 1912 to 1958 saw a gradual increase in the collection and analysis of samples from the historical eruptions of Kīlauea and Mauna Loa and development of the concepts needed to evaluate them. In a classic 1955 paper, Howard Powers introduced the concepts of magnesia variation diagrams, to display basaltic compositions, and olivine-control lines, to distinguish between possibly comagmatic and clearly distinct basaltic lineages. In particular, he and others recognized that Kīlauea and Mauna Loa basalts must have different sources. Subsequent years saw a great increase in petrologic data, as the development of the electron microprobe made it possible to routinely monitor glass and mineral compositions, in addition to bulk rock compositions. We now have 100 years’ worth of glass compositions for Kīlauea summit eruptions, which, together with expanding databases on prehistoric tephras, provide important constraints on the nature of Kīlauea’s summit reservoir. A series of chemically distinctive eruptions in the 1950s and 1960s facilitated evaluation of magma mixing and transport processes at Kīlauea. At Mauna Loa, lava compositions are distinctive only at the trace element level, suggesting that its summit reservoir is better mixed than Kīlauea’s. Most summit lavas at both volcanoes, however, lie on olivine control lines having the same olivine composition (Fo 86–87 ). Study of the ongoing East Rift Zone eruption at Kīlauea has further illuminated the complexity of magma storage, resupply, and mixing along this very active rift zone. Studies of active and closed-system lava lakes have been part of HVO’s efforts since Jaggar’s unique descriptions of the Halema‘uma‘u lava lake that existed before 1924. Detailed study of closed-system bodies, including the 1959 Kīlauea Iki, 1963 ‘Alae, and 1965 and prehistoric Makaopuhi lava lakes and the Uēkahuna laccolith, have allowed recognition and quantification of processes of basalt differentiation. Specific topics reviewed herein include the occurrence of segregation veins and related structures, overall cooling history, and patterns of crystallization and reequilibration of olivine in various lava lakes. In recent decades, study of the submarine slopes of the Island of Hawai‘i and of Lō‘ihi Seamount has revolutionized our understanding of the early history of Hawaiian volcanoes. Observations of Lō‘ihi lavas first established the existence of an early alkalic stage in the evolution of Hawaiian volcanoes. Stages of volcanic development from inception to tholeiitic shield building can be observed in Kīlauea’s submarine and subaerial sections. One distinctive feature of submarine volcanics at Kīlauea, Mauna Loa, and Hualālai is that picritic lavas are more abundant than in subaerial eruptions. Also, olivine compositions of submarine lavas are more magnesian, ranging from Fo 88 at Kīlauea to Fo 89 at Hualālai. The most magnesian glasses known from Kīlauea (MgO=14.7–15.0 weight percent) were found along the submarine part of Kīlauea’s East Rift Zone. Contributions to our knowledge of the nature of the mantle source(s) of Hawaiian basalts are reviewed briefly, although this is a topic where debate is ongoing. Finally, our accumulated petrologic observations impose constraints on the nature of the summit reservoirs at Kīlauea and Mauna Loa, specifically whether the summit chamber has been continuous or segmented during past decades.

Hawaii↗
USGS2017

Beryllium

Beryllium is a mineral commodity that is used in a variety of industries to make products that are essential for the smooth functioning of a modern society. Two minerals, bertrandite (which is supplied domestically) and beryl (which is currently supplied solely by imports), are necessary to ensure a stable supply of high-purity beryllium metal, alloys, and metal-matrix composites and beryllium oxide ceramics. Although bertrandite is the source mineral for more than 90 percent of the beryllium produced globally, industrial beryl is critical for the production of the very high purity beryllium metal needed for some strategic applications. The current sole domestic source of beryllium is bertrandite ore from the Spor Mountain deposit in Utah; beryl is imported mainly from Brazil, China, Madagascar, Mozambique, and Portugal. High-purity beryllium metal is classified as a strategic and critical material by the Strategic Materials Protection Board of the U.S. Department of Defense because it is used in products that are vital to national security. Beryllium is maintained in the U.S. stockpile of strategic materials in the form of hot-pressed beryllium metal powder. Because of its unique chemical properties, beryllium is indispensable for many important industrial products used in the aerospace, computer, defense, medical, nuclear, and telecommunications industries. For example, high-performance alloys of beryllium are used in many specialized, high-technology electronics applications, as they are energy efficient and can be used to fabricate miniaturized components. Beryllium-copper alloys are used as contacts and connectors, switches, relays, and shielding for everything from cell phones to thermostats, and beryllium-nickel alloys excel in producing wear-resistant and shape-retaining high-temperature springs. Beryllium metal composites, which combine the fabrication ability of aluminum with the thermal conductivity and highly elastic modulus of beryllium, are ideal for producing aircraft and satellite structural components that have a high stiffness-to-weight ratio and low surface vibration. Beryllium oxide ceramics are used in a wide range of applications, including missile guidance systems, radar applications, and cell phone transmitters, and they are critical to medical technologies, such as magnetic resonance imaging (MRI) machines, medical lasers, and portable defibrillators. The United States is expected to remain self-sufficient with respect to most of its beryllium requirements, based on information available at the time this chapter was prepared (2013). The United States is one of only three countries that currently process beryllium ores and concentrate them into beryllium products, and these three countries supply most of the rest of the world with these products. Exploration for new deposits in the United States is limited because domestic beryllium production is dominated by a single producer that effectively controls the domestic beryllium market, which is relatively small and specialized, and the market cannot readily accommodate new competition on the raw material supply side.

Professional Paper↗
USGS2017

Germanium and indium

Germanium and indium are two important elements used in electronics devices, flat-panel display screens, light-emitting diodes, night vision devices, optical fiber, optical lens systems, and solar power arrays. Germanium and indium are treated together in this chapter because they have similar technological uses and because both are recovered as byproducts, mainly from copper and zinc sulfides. The world’s total production of germanium in 2011 was estimated to be 118 metric tons. This total comprised germanium recovered from zinc concentrates, from fly ash residues from coal burning, and from recycled material. Worldwide, primary germanium was recovered in Canada from zinc concentrates shipped from the United States; in China from zinc residues and coal from multiple sources in China and elsewhere; in Finland from zinc concentrates from the Democratic Republic of the Congo; and in Russia from coal. World production of indium metal was estimated to be about 723 metric tons in 2011; more than one-half of the total was produced in China. Other leading producers included Belgium, Canada, Japan, and the Republic of Korea. These five countries accounted for nearly 95 percent of primary indium production. Deposit types that contain significant amounts of germanium include volcanogenic massive sulfide (VMS) deposits, sedimentary exhalative (SEDEX) deposits, Mississippi Valley-type (MVT) lead-zinc deposits (including Irish-type zinc-lead deposits), Kipushi-type zinc-lead-copper replacement bodies in carbonate rocks, and coal deposits. More than one-half of the byproduct indium in the world is produced in southern China from VMS and SEDEX deposits, and much of the remainder is produced from zinc concentrates from MVT deposits. The Laochang deposit in Yunnan Province, China, and the VMS deposits of the Murchison greenstone belt in Limpopo Province, South Africa, provide excellent examples of indium-enriched deposits. The SEDEX deposits at Bainiuchang, China (located in southeastern Yunnan Province), and the Dabaoshan SEDEX deposit (located in the Nanling region of China) contain indium-enriched sphalerite. Another major potential source of indium occurs in the polymetallic tin-tungsten belt in the Eastern Cordillera of the Andes Mountains of Bolivia. Deposits there occur as dense arrays of narrow, elongate, indium-enriched tin oxide-polymetallic sulfide veins in volcanic rocks and porphyry stocks. Information about the behavior of germanium and indium in the environment is limited. In surface weathering environments, germanium and indium may dissolve from host minerals and form complexes with chloride, fluoride, hydroxide, organic matter, phosphate, or sulfate compounds. The tendency for germanium and indium to be dissolved and transported largely depends upon the pH and temperature of the weathering solutions. Because both elements are commonly concentrated in sulfide minerals, they can be expected to be relatively mobile in acid mine drainage where oxidative dissolution of sulfide minerals releases metals and sulfuric acid, resulting in acidic pH values that allow higher concentrations of metals to be dissolved into solution.

Professional Paper↗
USGS2017

Graphite

Graphite is a form of pure carbon that normally occurs as black crystal flakes and masses. It has important properties, such as chemical inertness, thermal stability, high electrical conductivity, and lubricity (slipperiness) that make it suitable for many industrial applications, including electronics, lubricants, metallurgy, and steelmaking. For some of these uses, no suitable substitutes are available. Steelmaking and refractory applications in metallurgy use the largest amount of produced graphite; however, emerging technology uses in large-scale fuel cell, battery, and lightweight high-strength composite applications could substantially increase world demand for graphite. Graphite ores are classified as “amorphous” (microcrystalline), and “crystalline” (“flake” or “lump or chip”) based on the ore’s crystallinity, grain-size, and morphology. All graphite deposits mined today formed from metamorphism of carbonaceous sedimentary rocks, and the ore type is determined by the geologic setting. Thermally metamorphosed coal is the usual source of amorphous graphite. Disseminated crystalline flake graphite is mined from carbonaceous metamorphic rocks, and lump or chip graphite is mined from veins in high-grade metamorphic regions. Because graphite is chemically inert and nontoxic, the main environmental concerns associated with graphite mining are inhalation of fine-grained dusts, including silicate and sulfide mineral particles, and hydrocarbon vapors produced during the mining and processing of ore. Synthetic graphite is manufactured from hydrocarbon sources using high-temperature heat treatment, and it is more expensive to produce than natural graphite. Production of natural graphite is dominated by China, India, and Brazil, which export graphite worldwide. China provides approximately 67 percent of worldwide output of natural graphite, and, as the dominant exporter, has the ability to set world prices. China has significant graphite reserves, and China’s graphite production is expected to increase, although rising labor costs and some mine production problems are developing. China is expected to continue to be the dominant exporter for the near future. Mexico and Canada export graphite mainly to the United States, which has not had domestic production of natural graphite since the 1950s. Most graphite deposits in the United States are too small, low-grade, or remote to be of commercial value in the near future, and the likelihood of discovering larger, higher-grade, or favorably located domestic deposits is unlikely. The United States is a major producer of synthetic graphite.

Professional Paper↗
USGS2015

Arctic Alaska’s Lower Cretaceous (Hauterivian and Barremian) mudstone succession—Linking lithofacies, texture, and geochemistry to marine processes

We present new images and descriptions of the lithofacies and organic facies of the pebble shale unit and lower part of the Hue Shale (Lower Cretaceous) of Arctic Alaska at a high magnification that illustrates their textural characteristics. Our aims were to describe and determine the distribution of facies in these petroleum source rocks and to identify the processes that formed them. We sampled at high-resolution and applied new petrographic techniques combined with scanning electron microscopy and geochemical analyses to samples collected from three widely spaced sections—located in exposures along the Canning River and continuous core from the Mikkelsen Bay State 1 and Orion 1 wells. Results from these three locations indicate that this succession consists primarily of clay-rich mudstones that are variously silt- or sand-bearing and clay-dominated mudstones that exhibit mainly relict, 2–5 millimeter thick bedding and common but variable microbioturbation, rare macrobioturbation, and common fabrics of pelleted clay and silt. These mudstones contain rare, poorly sorted, silt-rich basal laminae that are often discontinuous and have wavy, sharp bases and crude upward fining. In addition, mud-supported, outsized clasts (dropstones) of fine sand to pebble size are present throughout the succession as isolated clasts or in clusters. We interpret these textures and much of this succession to result from intermittent deposition by suspension settling from melting seasonal sea ice—sometimes sediment-laden—and associated primary productivity. Overall, this mudstone succession fines and deepens upward from the pebble shale unit into the Hue Shale. In the Hue Shale of the Orion well, however, different processes intermittently deposited thin, discrete intervals of coarser sediment that probably represent deposition from density currents. Also in the Hue Shale of the Orion well, several thicker sandstone and silt-dominated mudstone units with discordant, scoured bases and cut and fill structures represent erosion during higher energy events such as major storms. Other lithofacies within the succession are graded tuffs/bentonites and tuffaceous/bentonitic mudstones from episodic volcanic ash falls; these are abundant in the Hue Shale, and very rare in the pebble shale unit of the two wells. Organic-carbon rich strata associated with volcanic ash intervals of the pebble shale unit and Hue Shale in the Mikkelsen 1 well have some of the best petroleum source rock potential determined for this succession. Authigenic pyrite and carbonate-cement-dominated mudstone are also present in both units of all three sections. The carbonate-cemented units indicate breaks in sedimentation and are common in the Hue Shale and in sections of the pebble shale unit interpreted to be more distal, such as along the Canning River. Our results document the variation in facies and textures of the Hauterivian and Barremian Lower Cretaceous mudstone succession of Arctic Alaska. Comparison of these characteristics to the products of modern processes on the North Slope of Alaska, in the Beaufort Sea, and elsewhere suggest that this succession formed primarily from depositional processes related to seasonal sea ice with intermittent fluvial-sourced sediment deposited by density currents and episodic erosion and reworking by storms and other currents.

Alaska↗
USGS2023

Chromium in minerals and selected aquifer materials

Between 1952 and 1964, hexavalent chromium, Cr(VI), was released into groundwater from a Pacific Gas and Electric Company (PG&E) compressor station in Hinkley, California, in the western Mojave Desert 80 miles northeast of Los Angeles, California. In 2015, the extent of anthropogenic Cr(VI) in groundwater in Hinkley and Water Valleys was uncertain, but some Cr(VI) in groundwater may be naturally occurring from rock and aquifer material. To evaluate potential sources of natural Cr(VI), chromium and other selected trace-element concentrations were measured by inductively coupled plasma-mass spectrometry (ICP-MS), with multi-acid digestion, on 34 samples of surficial alluvium and core material from Hinkley and Water Valleys, California, and on 2 samples of alluvium from the mafic Sheep Creek fan to the southwest. Chromium concentrations in Hinkley and Water Valleys ranged from 2 to 110 milligrams per kilogram (mg/kg), with a median concentration of 14 mg/kg; concentrations were highest in weathered mafic hornblende diorite associated with Iron Mountain. High chromium concentrations also were present within fine-textured materials and visually abundant iron- and manganese-oxide coatings on the surfaces of mineral grains. For comparison, chromium concentrations as high as 170 mg/kg were measured in mafic alluvium from the Sheep Creek fan. In contrast, chromium concentrations were lowest in Mojave-type deposits (Mojave River stream and lake margin deposits), with a median of 6 mg/kg. Chromium concentrations measured by ICP-MS compared favorably with concentrations measured by portable (handheld) X-ray fluorescence (pXRF; chapter B), on the basis of least-squares regression results and a coefficient of determination (R 2 ) of 0.97. Minerals in bulk samples and the heavy (dense) mineral fractions isolated from those samples were identified using optical techniques, X-ray diffraction (XRD), and scanning electron microscopy (SEM). Quartz and feldspar were the most abundant minerals, especially within recent and older Mojave River deposits. Chromium concentrations were as high as 1,250 mg/kg in the heavy-mineral fraction, with specific gravity greater than 3.32. Chromium was not commonly detected in the light-mineral fraction, with specific gravity less than 2.85. Most chromium within the heavy-mineral fraction was substituted within magnetite mineral grains less than 100 micrometers (μm) in diameter, and almost no chromite was present within the heavy-mineral fraction. Although magnetite is resistive to weathering, weathering of magnetite to hematite was identified (1) in Miocene materials underlying unconsolidated deposits in the western subarea of Hinkley Valley and (2) in alluvium within Water Valley that contains weathered minerals eroded from Miocene rock. Less-dense, more easily weathered chromium-containing amphiboles, such as actinolite in older Mojave River alluvium and hornblende in locally derived alluvium from Iron Mountain, were identified optically. Magnetite was not identified in weathered hornblende diorite and was less abundant in locally derived materials and in Miocene materials than in Mojave-type deposits. A comparison of ICP-MS data and sequential extraction data shows that approximately 90 percent of chromium in aquifer material within Hinkley and Water Valleys was not extractable and was interpreted to reside within unweathered mineral grains. Most extractable chromium was within the strong acid extractable fraction. Chromium within the weakly sorbed, and specifically sorbed extractable fractions in oxide accumulations within the regulatory Cr(VI) plume is potentially mobile into groundwater with changes in ionic strength or pH. Although Hinkley and Water Valleys are regionally low in chromium, natural geologic sources of chromium may be present in aquifer materials penetrated by wells completed in (1) weathered hornblende diorite bedrock underlying the western subarea; (2) Miocene deposits underlying the western subarea and unconsolidated material in the northern subarea and Water Valley containing basalt or weathered minerals eroded from Miocene deposits; (3) unconsolidated material containing visually abundant iron- and manganese-oxide coatings on the surfaces of mineral grains that are present near the water table and near lithologic or geologic contacts; and (4) brown clay and mudflat/playa deposits in the northern subarea. Brown clay and mudflat/playa deposits in the eastern subarea near Mount General have a low-chromium, felsic mineralogy similar to Mojave River deposits and do not contain high concentrations of chromium; however, manganese(IV) oxides within these materials may facilitate oxidation of trivalent chromium, Cr(III), to Cr(VI).

California↗
USGS2023

Sequestration and reoxidation of chromium in experimental microcosms

Groundwater containing hexavalent chromium, Cr(VI), downgradient from the Pacific Gas and Electric Company (PG&E) Hinkley compressor station in the Mojave Desert, 80 miles northeast of Los Angeles, California, is undergoing bioremediation using added ethanol as a reductant in a volume of the aquifer defined as the in situ reactive zone (IRZ). This treatment reduces Cr(VI) to trivalent chromium, Cr(III), which is rapidly sequestered by sorption to aquifer particle surfaces and by co-precipitation within iron (Fe) or manganese (Mn) bearing minerals forming in place as reduction proceeds. Successful mitigation of the Cr(VI) plume is projected to require 10–95 years, at which time bioremediation with ethanol will likely cease. This projection assumes that Cr(VI) removal is permanent and that no Cr(III) will oxidize back to Cr(VI) in the event of changing hydrologic conditions that may cause oxygen-rich water to re-enter the IRZ. Laboratory microcosm experiments were done to explore the process of reductive sequestration of Cr(VI) to Cr(III) and the potential for reoxidation of Cr(III) to Cr(VI). In reductive sequestration experiments, batch microcosms were prepared with aquifer materials collected from sites upgradient of the Cr(VI) regulatory plume. Control microcosms were prepared using Fe- and Mn-coated quartz sand. Unfiltered Mojave River groundwater containing an added tracer of isotopically labeled chromium-50 were reacted with microcosm materials for up to 2 years; during this time, bio-reduction was stimulated by repeated additions of diluted ethanol to maintain reduced conditions within appropriate ranges, avoiding sulfate reducing or methanogenic conditions as much as possible while mimicking field conditions. Analysis of chromium-50, Fe, and Mn obtained by sequential extraction from microcosms harvested (incubation terminated and microcosm contents analyzed) at various times showed that some aqueous chromium (Cr) was sorbed to particle surfaces within hours; reduction to Cr(III) and incorporation into amorphous and crystalline solid phases occurred during the next few months. Amorphous Cr-containing fractions included Fe and Mn hydroxides and organic matter. Ultimately, most of the chromium-50 tracer was present in the less reactive crystalline phase. However, Fe and Mn were broadly distributed at later stages of reduction, and both were spatially co-located with Cr on a micrometer (μm) scale. Solid-phase data collected using scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS) and X-ray absorption spectroscopy (XAS) indicated that some Cr(III) was associated with mixed valence Fe oxides like magnetite and Fe-Mn oxides like jacobsite. Additionally, Cr(III) was observed within several μm of Fe and Mn embedded in clays and in mineral coatings. To evaluate the potential for reoxidation of Cr(III) to Cr(VI), additional batch microcosms of aquifer materials and mixtures of Fe- and Mn-coated sand were first reduced for more than 1 year and subsequently oxidized for almost 2 years. Hexavalent chromium was formed and was available for release to the aqueous phase during oxidation of all materials; however, the timing and amount of Cr(VI) formed and released varied among substrates. Artificial substrates containing more Mn produced more Cr(VI). Site material characteristic of recent Mojave River deposits contained within the IRZ produced the least Cr(VI) during oxidation, while site materials composed of older Mojave River aquifer material (containing more Mn) produced more Cr(VI). Site material collected from within the IRZ contained more Cr but produced an intermediate amount of Cr(VI) following oxidation. The combined results of microcosm chemistry and solid-phase analyses showed that the nature and locus of Cr(III) sequestration influenced its vulnerability to reoxidation to Cr(VI). It was concluded that co-location of Cr with Mn at later stages of reduction influenced the susceptibility of Cr(III) to reoxidation in microcosms. Reoxidation of Cr(III) to Cr(VI) was observed in experiments with previously reduced material after just 14 days exposure to oxygen. As much as 10 percent of added Cr was oxidized to Cr(VI) in microcosms prepared using recent Mojave River aquifer material, and as much as 20 percent of added Cr was oxidized to Cr(VI) in microcosms prepared using older Mojave River aquifer material. Less Cr(VI) (less than 3 percent of Cr added before reduction) was released to the aqueous phase, and this release occurred following longer oxygen exposure. Site managers may need to plan for long-term monitoring and the possibility of active maintenance of anoxic conditions within the IRZ to ensure permanent sequestration of Cr after bioremediation with ethanol ceases.

California↗
USGS2005

Geologic map of the Ikpikpuk River quadrangle, Alaska

This map is a product of the USGS Digital Geologic Maps of Northern Alaska project, which captures in digital format quadrangles across the entire width of northern Alaska. Sources include geologic maps previously published in hardcopy format and recent updates and revisions based on field mapping by the Alaska Department of Natural Resources, Division of Geological and Geophysical Surveys and Division of Oil and Gas, and the U.S. Geological Survey. Individual quadrangles are digitized at either 1:125,000 or 1:250,000 depending on the resolution of source maps. The project objective is to produce a set of digital geologic maps with uniform stratigraphic nomenclature and structural annotation, and publish those maps electronically. The paper version of this map is available for purchase from the USGS Store.

Alaska↗
USGS2006

Geologic map of the Lookout Ridge quadrangle, Alaska

This map is a product of the USGS Digital Geologic Maps of Northern Alaska project, which captures in digital format quadrangles across the entire width of northern Alaska. Sources include geologic maps previously published in hardcopy format and recent updates and revisions based on field mapping by the Alaska Department of Natural Resources, Division of Geological and Geophysical Surveys and Division of Oil and Gas, and the U.S. Geological Survey. Individual quadrangles are digitized at either 1:125,000 or 1:250,000 depending on the resolution of source maps. The project objective is to produce a set of digital geologic maps with uniform stratigraphic nomenclature and structural annotation, and publish those maps electronically. The paper version of this map is available for purchase from the USGS Store.

Alaska↗
USGS2006

Geologic map of the Utukok River quadrangle, Alaska

This map is a product of the USGS Digital Geologic Maps of Northern Alaska project, which captures in digital format quadrangles across the entire width of northern Alaska. Sources include geologic maps previously published in hardcopy format and recent updates and revisions based on field mapping by the Alaska Department of Natural Resources, Division of Geological and Geophysical Surveys and Division of Oil and Gas, and the U.S. Geological Survey. Individual quadrangles are digitized at either 1:125,000 or 1:250,000 depending on the resolution of source maps. The project objective is to produce a set of digital geologic maps with uniform stratigraphic nomenclature and structural annotation, and publish those maps electronically.

Alaska↗
USGS2008

Geologic map of the Point Lay quadrangle, Alaska

This map is a product of the USGS Digital Geologic Maps of Northern Alaska project, which captures in digital format quadrangles across the entire width of northern Alaska. Sources include geologic maps previously published in hardcopy format and recent updates and revisions based on field mapping by the Alaska Department of Natural Resources, Division of Geological and Geophysical Surveys and Division of Oil and Gas, and the U.S. Geological Survey. Individual quadrangles are digitized at either 1:125,000 or 1:250,000 depending on the resolution of source maps. The project objective is to produce a set of digital geologic maps with uniform stratigraphic nomenclature and structural annotation, and publish those maps electronically. The paper version of this map is available for purchase from the USGS Store.

Alaska↗