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.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802E","isbn":"978-1-4113-3991-0","usgsCitation":"Foley, N.K., Jaskula, B.W., Piatak, N.M., and Schulte, R.F., 2017, Beryllium, chap. E of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. E1–E32, https://doi.org/10.3133/pp1802E.","productDescription":"viii, 32 p.","numberOfPages":"44","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-045146","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334565,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/e/pp1802e.pdf","text":"Report","size":"15.7 MB","linkFileType":{"id":1,"text":"pdf"},"description":"Professional Paper 1802 E"},{"id":334564,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/e/coverthb1.jpg"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Niobium and tantalum are transition metals that are almost always found together in nature because they have very similar physical and chemical properties. Their properties of hardness, conductivity, and resistance to corrosion largely determine their primary uses today. The leading use of niobium (about 75 percent) is in the production of high-strength steel alloys used in pipelines, transportation infrastructure, and structural applications. Electronic capacitors are the leading use of tantalum for high-end applications, including cell phones, computer hard drives, and such implantable medical devices as pacemakers. Niobium and tantalum are considered critical and strategic metals based on the potential risks to their supply (because current production is restricted to only a few countries) and the significant effects that a restriction in supply would have on the defense, energy, high-tech industrial, and medical sectors.
The average abundance of niobium and tantalum in bulk continental crust is relatively low—8.0 parts per million (ppm) niobium and 0.7 ppm tantalum. Their chemical characteristics, such as small ionic size and high electronic field strength, significantly reduce the potential for these elements to substitute for more common elements in rock-forming minerals and make niobium and tantalum essentially immobile in most aqueous solutions. Niobium and tantalum do not occur naturally as pure metals but are concentrated in a variety of relatively rare oxide and hydroxide minerals, as well as in a few rare silicate minerals. Niobium is primarily derived from the complex oxide minerals of the pyrochlore group ((Na,Ca,Ce)2(Nb,Ti,Ta)2(O,OH,F)7), which are found in some alkaline granite-syenite complexes (that is, igneous rocks containing sodium- or potassium-rich minerals and little or no quartz) and carbonatites (that is, igneous rocks that are more than 50 percent composed of primary carbonate minerals, by volume). Tantalum is derived mostly from the mineral tantalite ((Fe,Mn)(Ta,Nb)2O6), which is found as an accessory mineral in rare-metal granites and pegmatites that are also enriched in lithium and cesium (termed lithium-cesium-tantalum (LCT)-type pegmatites).
Brazil and Canada are the leading nations that produce niobium mineral concentrates, but Brazil is by far the leading producer, accounting for about 90 percent of production, which comes mostly from weathered material derived from carbonatites. Brazil and Canada also have the largest identified niobium resources; additional resources, although they are less well reported, occur in Angola, Australia, China, Greenland, Malawi, Russia, and South Africa. Australia and Brazil have been the leading producers of tantalum mineral concentrates, although recently Ethiopia and Mozambique have also been significant suppliers of tantalum. Artisanal mining of columbite-tantalite (also called coltan) is practiced in many countries, particularly Burundi, the Democratic Republic of the Congo (Congo [Kinshasa]), Nigeria, Rwanda, and Uganda. Brazil has about 40 percent of the identified tantalum resources; other countries and regions with identified tantalum resources include, in decreasing order of resources, Australia, Asia, Russia and the Middle East, Africa, North America, and Europe. Identified niobium and tantalum resources in the United States are small, low grade, and difficult to recover and process, and are thus not commercially recoverable at current prices. Consequently, the United States meets its current and expected future needs for niobium and tantalum through imports of primary mineral concentrates and alloys and through recovery from foreign and domestic alloy scrap that contain the metals.
Environmentally, the main issues related to niobium and tantalum mining are land disruptions, the volume of waste materials and their disposal, and the radioactivity of some tailings and waste materials that contain thorium and uranium. Because of the relative biological inertness of niobium and tantalum, human and ecological health concerns are generally minimal under most natural conditions.
Demand for both niobium and tantalum is expected to increase as the world economy continues to recover from the downturn that began in 2008. Increased demand for niobium is linked to increased consumption of microalloyed steel, which is used in the manufacture of cars, buildings, ships, and refinery equipment. Demand for these steels will likely increase with continued economic development in such countries as Brazil, China, and India. In addition, increased global demand for cars, cell phones, computers, superconducting magnets, and other high-tech devices will likely spur increased demand for both niobium and tantalum. The estimated global reserves and resources of niobium and tantalum are large and appear more than sufficient to meet global demand for the foreseeable future, possibly the next 500 years. The sale of “conflict coltan” attributed to rebel forces waging a civil war in Congo (Kinshasa) has been of recent concern and has highlighted the need for a transparent and traceable global supply chain that can exclude illegal columbite-tantalite from the conventional market while discerning legitimate artisanal mine production in central Africa.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802M","isbn":"978-1-4113-3991-0","usgsCitation":"Schulz, K.J., Piatak, N.M., and Papp, J.F., 2017, Niobium and tantalum, chap. M of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. M1–M34, https://doi.org/10.3133/pp1802M.","productDescription":"viii, 34 p.","numberOfPages":"46","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-045581","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334595,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/m/coverthb1.jpg"},{"id":334596,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/m/pp1802m.pdf","text":"Report","size":"15.2 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 M"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
The platinum-group elements (PGEs)—platinum, palladium, rhodium, ruthenium, iridium, and osmium—are metals that have similar physical and chemical properties and tend to occur together in nature. PGEs are indispensable to many industrial applications but are mined in only a few places. The availability and accessibility of PGEs could be disrupted by economic, environmental, political, and social events. The United States net import reliance as a percentage of apparent consumption is about 90 percent.
PGEs have many industrial applications. They are used in catalytic converters to reduce carbon monoxide, hydrocarbon, and nitrous oxide emissions in automobile exhaust. The chemical industry requires platinum or platinum-rhodium alloys to manufacture nitric oxide, which is the raw material used to manufacture explosives, fertilizers, and nitric acid. In the petrochemical industry, platinum-supported catalysts are needed to refine crude oil and to produce aromatic compounds and high-octane gasoline. Alloys of PGEs are exceptionally hard and durable, making them the best known coating for industrial crucibles used in the manufacture of chemicals and synthetic materials. PGEs are used by the glass manufacturing industry in the production of fiberglass and flat-panel and liquid crystal displays. In the electronics industry, PGEs are used in computer hard disks, hybridized integrated circuits, and multilayer ceramic capacitors.
Aside from their industrial applications, PGEs are used in such other fields as health, consumer goods, and finance. Platinum, for example, is used in medical implants, such as pacemakers, and PGEs are used in cancer-fighting drugs. Platinum alloys are an ideal choice for jewelry because of their white color, strength, and resistance to tarnish. Platinum, palladium, and rhodium in the form of coins and bars are also used as investment commodities, and various financial instruments based on the value of these PGEs are traded on major exchanges.
PGEs are among the rarest metals; Earth’s upper crust contains only about 0.0005 part per million (ppm) platinum. Today, the average grade of PGEs in ores that are mined primarily for their PGE concentrations varies from 5 to 15 ppm, although the concentration of PGEs in hand-picked ore specimens may range from tens to hundreds of parts per million.
More than 100 different minerals have one of the PGEs as an essential component. PGE minerals occur as native metals. They also occur as compounds with other transition metals (copper, iron, mercury, nickel, and silver), post-transition metals (bismuth, lead, and tin), metalloids (antimony, arsenic, and tellurium), and nonmetals (selenium and sulfur).
From 1900 to 2011, approximately 14,200 metric tons of PGEs was produced, and roughly 95 percent of that production (13,500 metric tons) took place between 1960 and 2011. The breakdown of production by country shows that, since 1900, about 90 percent of the production came from South Africa and Russia. The secondary supply of platinum, palladium, and rhodium is obtained through the recycling of catalytic converters from end-of-life vehicles, jewelry, and electronic equipment. Recycled platinum, palladium, and rhodium provide a significant proportion of the world’s total supply; these secondary sources are sufficient to close the gap between world mine production and consumption.
Exploration and mining companies report resources of about 104,000 metric tons of PGEs (including minor amounts of gold) in mineral deposits around the world that could be developed. For PGEs, almost all the reported production and identified resources are associated with deposits in three geologic features—the Bushveld Complex, which is a layered mafic-to-ultramafic intrusion in South Africa; the Great Dyke, which is a layered mafic-to-ultramafic intrusion in Zimbabwe; and sill-like intrusions associated with flood basalts in the Noril’sk-Talnakh area of Russia.
The metallic forms of PGEs are generally considered to be inert. PGEs pose a risk to human health only in cases where individuals are occupationally exposed to synthetic PGE compounds, especially workers in precious-metal refineries. In the natural environment, background PGE concentrations are low in water, sediment, soil, and plants. Anthropogenic sources of PGEs in the environment include catalytic converters used in modern automobiles, platinum-based chemotherapy drugs, and smelter emissions.
The abundance of sulfide minerals defines the environmental and geologic characteristics of PGE-enriched magmatic sulfide deposits; those deposits with the highest amount of sulfide minerals could have the highest environmental impact. Acid rock drainage from reef-type and contact-type deposits is unlikely because the ores and their host rocks contain low proportions of sulfide minerals. For some conduit-type orebodies with massive ores, mineral-processing techniques separate and produce concentrates of copper-, iron-, and nickel-bearing sulfide minerals; those with copper and nickel are processed to extract metal, but the iron-sulfide minerals, mainly pyrrhotite, are discarded as waste. This results in waste material with a high acid-generating potential.
The most significant primary source of PGEs in the United States is a deposit in the Stillwater Complex, which is a layered igneous intrusion in Montana. Approximately 305 metric tons of platinum and palladium have been mined from the Stillwater Complex deposit since 1986. Exploration and development drilling indicate that another 2,200 metric tons are present. Mining has progressed to depths of 1,800 meters below the surface, but the bottom of the ore deposit has not been reached; geologic estimates suggest that another 1,000 to 6,200 metric tons of PGEs could be present at depth. In the future, PGEs may be mined from deposits found near the base of the Duluth Complex, which is a group of igneous intrusions in Minnesota.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802N","isbn":"978-1-4113-3991-0","usgsCitation":"Zientek, M.L., Loferski, P.J., Parks, H.L., Schulte, R.F., and Seal, R.R., II, 2017, Platinum-group elements, chap. N of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. N1–N91, https://doi.org/10.3133/pp1802N.","productDescription":"ix, 91 p.","numberOfPages":"106","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-052035","costCenters":[{"id":312,"text":"Geology, Minerals, Energy, and Geophysics Science Center","active":true,"usgs":true}],"links":[{"id":334214,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/n/coverthb1.jpg"},{"id":334215,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/n/pp1802n.pdf","text":"Report","size":"33.4 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 N"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Vanadium is used primarily in the production of steel alloys; as a catalyst for the chemical industry; in the making of ceramics, glasses, and pigments; and in vanadium redox-flow batteries (VRBs) for large-scale storage of electricity. World vanadium resources in 2012 were estimated to be 63 million metric tons, which include about 14 million metric tons of reserves. The majority of the vanadium produced in 2012 was from China, Russia, and South Africa.
Vanadium is extracted from several different types of mineral deposits and from fossil fuels. These deposits include vanadiferous titanomagnetite (VTM) deposits, sandstone-hosted vanadium (with or without uranium) deposits (SSV deposits), and vanadium-rich black shales. VTM deposits are the principal source of vanadium and consist of magmatic accumulations of ilmenite and magnetite containing 0.2 to 1 weight percent vanadium pentoxide (V2O5). SSV deposits are another important source; these deposits have average ore grades that range from 0.1 to greater than 1 weight percent V2O5. The United States has been and is currently the main producer of vanadium from SSV deposits, particularly those on the Colorado Plateau. Vanadium-rich black shales occur in marine successions that were deposited in epeiric (inland) seas and on continental margins. Concentrations in these shales regularly exceed 0.18 weight percent V2O5 and can be as high as 1.7 weight percent V2O5. Small amounts of vanadium have been produced from the Alum Shale in Sweden and from ferrophosphorus slag generated during the reduction of phosphate to elemental phosphorus in ore from shales of the Phosphoria Formation in Idaho and Wyoming. Because vanadium enrichment occurs in beds that are typically only a few meters thick, most of the vanadiferous black shales are not currently economic, although they may become an important resource in the future. Significant amounts of vanadium are recovered as byproducts of petroleum refining, and processing of coal, tar sands, and oil shales may be important future sources.
Vanadium occurs in one of four oxidation states in nature: +2, +3, +4, and +5. The V3+ ion has an octahedral radius that is almost identical to that of (Fe3+) and (Al3+) and, therefore, it substitutes in ferromagnesian minerals. During weathering, much of the vanadium may partition into newly formed clay minerals, and it either remains in the +3 valence state or oxidizes to the +4 valence state, both of which are relatively insoluble. If erosion is insignificant but chemical leaching is intense, the residual material may be enriched in vanadium, as are some bauxites and laterites. During the weathering of igneous, residual, or sedimentary rocks, some vanadium oxidizes to the +5 valence state, especially in the intensive oxidizing conditions that are characteristic of arid climates.
The average contents of vanadium in the environment are as follows: soils [10 to 500 parts per million (ppm)]; streams and rivers [0.2 to 2.9 parts per billion (ppb)]; and coastal seawater (0.3 to 2.8 ppb). Concentrations of vanadium in soils (548 to 7,160 ppm) collected near vanadium mines in China, the Czech Republic, and South Africa are many times greater than natural concentrations in soils. Additionally, if deposits contain sulfide minerals such as chalcocite, pyrite, and sphalerite, high levels of acidity may be present if sulfide dissolution is not balanced by the presence of acid-neutralizing carbonate minerals. Some of the vanadium-bearing deposit types, particularly some SSV and black-shale deposits, contain appreciable amounts of carbonate minerals, which lowers the acid-generation potential.
Vanadium is a micronutrient with a postulated requirement for humans of less than 10 micrograms per day, which can be met through dietary intake. Primary and secondary drinking water regulations for vanadium are not currently in place in the United States. Vanadium toxicity is thought to result from an intake of more than 10 to 20 milligrams per day. Vanadium is essential for some biological processes and organisms. For example, some nitrogen-fixing bacteria require vanadium for producing enzymes necessary to convert nitrogen from the atmosphere into ammonia, which is a more biologically accessible form of nitrogen.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802U","isbn":"978-1-4113-3991-0","usgsCitation":"Kelley, K.D., Scott, C.T., Polyak, D.E., and Kimball, B.E., 2017, Vanadium, chap. U of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. U1–U36, https://doi.org/10.3133/pp1802U.","productDescription":"viii, 36 p.","numberOfPages":"48","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-069568","costCenters":[{"id":171,"text":"Central Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334857,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/u/coverthb1.jpg"},{"id":334858,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/u/pp1802u.pdf","text":"Report","size":"10.2 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 U"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Cobalt is a silvery gray metal that has diverse uses based on certain key properties, including ferromagnetism, hardness and wear-resistance when alloyed with other metals, low thermal and electrical conductivity, high melting point, multiple valences, and production of intense blue colors when combined with silica. Cobalt is used mostly in cathodes in rechargeable batteries and in superalloys for turbine engines in jet aircraft. Annual global cobalt consumption was approximately 75,000 metric tons in 2011; China, Japan, and the United States (in order of consumption amount) were the top three cobalt-consuming countries. In 2011, approximately 109,000 metric tons of recoverable cobalt was produced in ores, concentrates, and intermediate products from cobalt, copper, nickel, platinum-group-element (PGE), and zinc operations. The Democratic Republic of the Congo (Congo [Kinshasa]) was the principal source of mined cobalt globally (55 percent). The United States produced a negligible amount of byproduct cobalt as an intermediate product from a PGE mining and refining operation in southeastern Montana; no U.S. production was from mines in which cobalt was the principal commodity. China was the leading refiner of cobalt, and much of its production came from cobalt ores, concentrates, and partially refined materials imported from Congo (Kinshasa).
The mineralogy of cobalt deposits is diverse and includes both primary (hypogene) and secondary (supergene) phases. Principal terrestrial (land-based) deposit types, which represent most of world’s cobalt mine production, include primary magmatic Ni-Cu(-Co-PGE) sulfides, primary and secondary stratiform sediment-hosted Cu-Co sulfides and oxides, and secondary Ni-Co laterites. Seven additional terrestrial deposit types are described in this chapter. The total terrestrial cobalt resource (reserves plus other resources) plus past production, where available, is calculated to be 25.5 million metric tons. Additional resources of cobalt are known to occur on the modern sea floor in aerially extensive deposits of Fe-Mn(-Ni-Cu-Co-Mo) nodules and Fe-Mn(-Co-Mo-rare-earth-element) crusts. Legal, economic, and technological barriers have prevented exploitation of these cobalt resources, which lie at water depths of as great as 6,000 meters, although advances in technology may soon allow production of these resources to be economically viable.
Environmental issues related to cobalt mining concern mainly the elevated cobalt contents in soils and waters. Although at low levels cobalt is essential to human health (it is the central atom in the critical nutrient vitamin B12), overexposure to high levels of cobalt may cause lung and heart dysfunction, as well as dermatitis. The ecological impacts of cobalt vary widely and can be severe for some species of fish and plants, depending on various environmental factors.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802F","isbn":"978-1-4113-3991-0","usgsCitation":"Slack, J.F., Kimball, B.E., and Shedd, K.B., 2017, Cobalt, chap. F of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. F1–F40, https://doi.org/10.3133/pp1802F.","productDescription":"viii, 40 p.","numberOfPages":"52","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-078704","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":339507,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/f/pp1802f.pdf","text":"Report ","size":"4.44 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 F"},{"id":339523,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/f/coverthb1.jpg"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Rhenium is one of the rarest elements in Earth’s continental crust; its estimated average crustal abundance is less than 1 part per billion. Rhenium is a metal that has an extremely high melting point and a heat-stable crystalline structure. More than 80 percent of the rhenium consumed in the world is used in high-temperature superalloys, especially those used to make turbine blades for jet aircraft engines. Rhenium’s other major application is in platinum-rhenium catalysts used in petroleum refining.
Rhenium rarely occurs as a native element or as its own sulfide mineral; most rhenium is present as a substitute for molybdenum in molybdenite. Annual world mine production of rhenium is about 50 metric tons. Nearly all primary rhenium production (that is, rhenium produced by mining rather than through recycling) is as a byproduct of copper mining, and about 80 percent of the rhenium obtained through mining is recovered from the flue dust produced during the roasting of molybdenite concentrates from porphyry copper deposits. Molybdenite in porphyry copper deposits can contain hundreds to several thousand grams per metric ton of rhenium, although the estimated rhenium grades of these deposits range from less than 0.1 gram per metric ton to about 0.6 gram per metric ton.
Continental-arc porphyry copper-(molybdenum-gold) deposits supply most of the world’s rhenium production and have large inferred rhenium resources. Porphyry copper mines in Chile account for about 55 percent of the world’s mine production of rhenium; rhenium is also recovered from porphyry copper deposits in the United States, Armenia, Kazakhstan, Mexico, Peru, Russia, and Uzbekistan. Sediment-hosted strata-bound copper deposits in Kazakhstan (of the sandstone type) and in Poland (of the reduced-facies, or Kupferschiefer, type) account for most other rhenium produced by mining. These types of deposits also have large amounts of identified rhenium resources. The future supply of rhenium is likely to depend largely on the capacity of the specialized processing facilities needed to recover rhenium from molybdenite concentrates.
The environmental consequences of rhenium recovery are closely linked to the consequences of mining large porphyry copper and strata-bound copper deposits; no additional environmental impact from recovery of rhenium from these deposits has been identified. No information is available regarding the potential toxic effects of rhenium on humans, partly because of the low natural abundance of rhenium.
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U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Selenium (Se) was discovered in 1817 in pyrite from copper mines in Sweden. It is a trace element in Earth’s crust, with an abundance of three to seven orders of magnitude less than the major rock-forming elements. Commercial use of selenium began in the United States in 1910, when it was used as a pigment for paints, ceramic glazes, and red glass. Since that time, it has had many other economic uses—notably, in the 1930s and 1940s, when it was used in rectifiers (which change alternating current to direct current), and in the 1960s, when it began to be used in the liner of photocopier drums. In the 21st century, other compounds have replaced selenium in these older products; modern uses for selenium include energy-efficient windows that limit heat transfer and thin-film photovoltaic cells that convert solar energy into electricity.
In Earth’s crust, selenium is found as selenide minerals, selenate and selenite salts, and as substitution for sulfur in sulfide minerals. It is the sulfide minerals, most commonly those in porphyry copper deposits, that provide the bulk of the selenium produced for the international commodity market. Selenium is obtained as a byproduct of copper refining and recovered from the anode slimes generated in electrolytic production of copper. Because of this, the countries that have the largest resources and (or) reserves of copper also have the largest resources and (or) reserves of selenium.
Because selenium occurs naturally in Earth’s crust, its presence in air, water, and soil results from both geologic reactions and human activity. Selenium is found concentrated naturally in soils that overlie bedrock with high selenium concentrations. Selenium mining, processing, use in industrial and agricultural applications, and disposal may all contribute selenium to the environment. A well-known case of selenium contamination from agricultural practices was discovered in 1983 in the Kesterson National Wildlife Refuge in California. There, waters draining from agricultural fields created wetlands with high concentrations of dissolved selenium in the water. The selenium was taken up by aquatic wildlife and caused massive numbers of embryonic deformities and deaths.
Regulatory agencies have since worked to safeguard ecological and human health by creating environmental exposure guidelines based upon selenium concentrations in water and in fish tissue. Any attempt to regulate selenium concentrations requires a delicate balance because selenium occurs naturally and is also a vital nutrient for the health of wildlife, domestic stock, and humans. Selenium is commonly added as a vitamin to animal feed, and in some regions of the United States and the world, it is added as an amendment to soils for uptake by agricultural crops.
The important role of selenium in economic products, energy supply, agriculture, and health will continue for well into the future. The challenge to society is to balance the benefits of selenium use with the environmental consequences of its extraction. Increased understanding of the elemental cycle of selenium in the earth may lead to new (or unconventional) sources of selenium, the discovery of new methods of extraction, and new technologies for minimizing the transfer of selenium from rock to biota, so to protect environmental and human health.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802Q","isbn":"978-1-4113-3991-0","usgsCitation":"Stillings, L.L., 2017, Selenium, chap. Q of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. Q1–Q55, https://doi.org/10.3133/pp1802Q.","productDescription":"viii, 55 p.","numberOfPages":"68","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-059321","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":335230,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/q/coverthb.jpg"},{"id":335231,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/q/pp1802q.pdf","text":"Report","size":"9.55 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 Q"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
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.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802J","usgsCitation":"Robinson, G.R., Jr., Hammarstrom, J.M., and Olson, D.W., 2017, Graphite, chap. J of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. J1–J24, https://doi.org/10.3133/pp1802J.","productDescription":"viii, 24 p.","numberOfPages":"36","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-044217","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334578,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/j/pp1802j.pdf","text":"Report","size":"4.30 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 J"},{"id":334577,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/j/coverthb1.jpg"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
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.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802I","isbn":"978-1-4113-3991-0","usgsCitation":"Shanks, W.C.P., III, Kimball, B.E., Tolcin, A.C., and Guberman, D.E., 2017, Germanium and indium, chap. I of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. I1–I27, https://doi.org/10.3133/pp1802I.","productDescription":"viii, 27 p.","numberOfPages":"39","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-052088","costCenters":[{"id":171,"text":"Central Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334573,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/i/coverthb1.jpg"},{"id":334574,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/i/pp1802i.pdf","text":"Report","size":"1.84 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 I"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Zirconium and hafnium are corrosion-resistant metals that are widely used in the chemical and nuclear industries. Most zirconium is consumed in the form of the main ore mineral zircon (ZrSiO4, or as zirconium oxide or other zirconium chemicals. Zirconium and hafnium are both refractory lithophile elements that have nearly identical charge, ionic radii, and ionic potentials. As a result, their geochemical behavior is generally similar. Both elements are classified as incompatible because they have physical and crystallochemical properties that exclude them from the crystal lattices of most rock-forming minerals. Zircon and another, less common, ore mineral, baddeleyite (ZrO2), form primarily as accessory minerals in igneous rocks. The presence and abundance of these ore minerals in igneous rocks are largely controlled by the element concentrations in the magma source and by the processes of melt generation and evolution. The world’s largest primary deposits of zirconium and hafnium are associated with alkaline igneous rocks, and, in one locality on the Kola Peninsula of Murmanskaya Oblast, Russia, baddeleyite is recovered as a byproduct of apatite and magnetite mining. Otherwise, there are few primary igneous deposits of zirconium- and hafnium-bearing minerals with economic value at present. The main ore deposits worldwide are heavy-mineral sands produced by the weathering and erosion of preexisting rocks and the concentration of zircon and other economically important heavy minerals, such as ilmenite and rutile (for titanium), chromite (for chromium), and monazite (for rare-earth elements) in sedimentary systems, particularly in coastal environments. In coastal deposits, heavy-mineral enrichment occurs where sediment is repeatedly reworked by wind, waves, currents, and tidal processes. The resulting heavy-mineral-sand deposits, called placers or paleoplacers, preferentially form at relatively low latitudes on passive continental margins and supply 100 percent of the world’s zircon. Zircon makes up a relatively small percentage of the economic heavy minerals in most deposits and is produced primarily as a byproduct of heavy-mineral-sand mining for titanium minerals.
From 2003 to 2012, world zirconium mineral concentrates production increased by more than 40 percent, and Australia and South Africa were the leading producers. Global consumption of zirconium mineral concentrates generally increased during the same time period, largely as a result of increased demand in developing economies in Asia and the Middle East. Global demand weakened in 2012, causing a decrease in world production of zirconium mineral concentrates and delaying the development of several new mining projects. Global consumption is expected to increase in the future, however, as demand from the ceramics, chemicals, and metals industries increases (driven by renewed growth in developing economies) and demand for zirconium and hafnium metal increases (driven by the construction and operation of new nuclear powerplants).
The behaviors of zirconium and hafnium in the environment are very similar to one another in that most zirconium- and hafnium-bearing minerals have limited solubility and reactivity. Anthropogenic sources of zirconium, and likely hafnium, are from industrial zirconium-containing byproducts and emissions from the processing of sponge zirconium, and exposure to the general population from these sources is small. Zirconium and hafnium are likely not essential to human health and generally are considered to be of low toxicity to humans. The main exposure risks are associated with industrial inhalation and dermal exposure. Because of the low solubility of zirconium and hafnium, ecological health concerns in the aquatic environment and in soils are minimal. Heavy-mineral-sand mining may lead to increased erosion rates when the mining is managed improperly. In addition, surface mining requires removal of the overlying organic soil layer and produces waste material that includes tailings and slimes. The soil removal and mining activity disturbs the surrounding ecosystem and alters the character of the landscape. Dry mineral separation processes create high amounts of airborne dust, whereas wet mineral separation processes do not. In operations that restore the landscape to pre-mining conditions, the volume of waste and the impact on the landscape may be relatively temporary.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802V","isbn":"978-1-4113-3991-0","usgsCitation":"Jones, J.V., III, Piatak, N.M., and Bedinger, G.M., 2017, Zirconium and hafnium, chap. V of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. V1–V26, https://doi.org/10.3133/pp1802V.","productDescription":"vii, 26 p.","numberOfPages":"38","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-049217","costCenters":[{"id":119,"text":"Alaska Science Center Geology Minerals","active":true,"usgs":true},{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":339506,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/v/pp1802v.pdf","text":"Report","size":"16.4 MB","description":"PP 1802 V"},{"id":339517,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/v/coverthb1.jpg"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Barite (barium sulfate, BaSO4) is vital to the oil and gas industry because it is a key constituent of the mud used to drill oil and gas wells. Elemental barium is an additive in optical glass, ceramic glazes, and other products. Within the United States, barite is produced mainly from mines in Nevada. Imports in 2011 (the latest year for which complete data were available) accounted for 78 percent of domestic consumption and came mostly from China.
Barite deposits can be divided into the following four main types: bedded-sedimentary; bedded-volcanic; vein, cavity-fill, and metasomatic; and residual. Bedded-sedimentary deposits, which are found in sedimentary rocks with characteristics of high biological productivity during sediment accumulation, are the major sources of barite production and account for the majority of reserves, both in the United States and worldwide. In 2013, China and India were the leading producers of barite, and they have large identified resources that position them to be significant producers for the foreseeable future. The potential for undiscovered barite resources in the United States and in many other countries is considerable, however. The expected tight supply and rising costs in the coming years will likely be met by increased production from such countries as Kazakhstan, Mexico, Morocco, and Vietnam.
Barium has limited mobility in the environment and exposed barium in the vicinity of barite mines poses minimal risk to human or ecosystem health. Of greater concern is the potential for acidic metal-bearing drainage at sites where the barite ores or waste rocks contain abundant sulfide minerals. This risk is lessened naturally if the host rocks at the site are acid-neutralizing, and the risk can also be lessened by engineering measures.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802D","isbn":"978-1-4113-3991-0","usgsCitation":"Johnson, C.A., Piatak, N.M., and Miller, M.M., 2017, Barite (Barium), chap. D of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. D1–D18, https://doi.org/10.3133/pp1802D.","productDescription":"vii, 18 p.","numberOfPages":"30","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-045302","costCenters":[{"id":211,"text":"Crustal Geophysics and Geochemistry Science Center","active":true,"usgs":true},{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334561,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/d/coverthb1.jpg"},{"id":334562,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/d/pp1802d.pdf","text":"Report","size":"3.91 MB","linkFileType":{"id":1,"text":"pdf"}}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
httsp://minerals.usgs.gov
Gallium is a soft, silvery metallic element with an atomic number of 31 and the chemical symbol Ga. Gallium is used in a wide variety of products that have microelectronic components containing either gallium arsenide (GaAs) or gallium nitride (GaN). GaAs is able to change electricity directly into laser light and is used in the manufacture of optoelectronic devices (laser diodes, light-emitting diodes [LEDs], photo detectors, and solar cells), which are important for aerospace and telecommunications applications and industrial and medical equipment. GaAs is also used in the production of highly specialized integrated circuits, semiconductors, and transistors; these are necessary for defense applications and high-performance computers. For example, cell phones with advanced personal computer-like functionality (smartphones) use GaAs-rich semiconductor components. GaN is used principally in the manufacture of LEDs and laser diodes, power electronics, and radio-frequency electronics. Because GaN power transistors operate at higher voltages and with a higher power density than GaAs devices, the uses for advanced GaN-based products are expected to increase in the future. Gallium technologies also have large power-handling capabilities and are used for cable television transmission, commercial wireless infrastructure, power electronics, and satellites. Gallium is also used for such familiar applications as screen backlighting for computer notebooks, flat-screen televisions, and desktop computer monitors.
Gallium is dispersed in small amounts in many minerals and rocks where it substitutes for elements of similar size and charge, such as aluminum and zinc. For example, gallium is found in small amounts (about 50 parts per million) in such aluminum-bearing minerals as diaspore-boehmite and gibbsite, which form bauxite deposits, and in the zinc-sulfide mineral sphalerite, which is found in many mineral deposits. At the present time, gallium metal is derived mainly as a byproduct of the processing of bauxite ore for aluminum; lesser amounts of gallium metal are produced from the processing of sphalerite ore from three types of deposits (sediment-hosted, Mississippi Valley-type, and volcanogenic massive sulfide) for zinc. The United States is expected to meet its current and expected future needs for gallium through imports of primary, recycled, and refined gallium, as well as through domestic production of recycled and refined gallium. The U.S. Geological Survey estimates that world resources of gallium in bauxite exceed 1 billion kilograms, and a considerable quantity of gallium could be present in world zinc reserves.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston VA","doi":"10.3133/pp1802H","isbn":"978-1-4113-3991-0","usgsCitation":"Foley, N.K., Jaskula, B.W., Kimball, B.E., and Schulte, R.F., 2017, Gallium, chap. H of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. H1–H35, https://doi.org/10.3133/pp1802H.","productDescription":"viii, 35 p.","numberOfPages":"48","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-045147","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334570,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/h/coverthb1.jpg"},{"id":334571,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/h/pp1802h.pdf","text":"Report","size":"21.5 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 H"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Antimony is an important mineral commodity used widely in modern industrialized societies. The element imparts strength, hardness, and corrosion resistance to alloys that are used in many areas of industry, including in lead-acid storage batteries. Antimony’s leading use is as a fire retardant in safety equipment and in household goods, such as mattresses. The U.S. Government has considered antimony to be a critical mineral mainly because of its use in military applications. The great majority of the world’s antimony comes from China, and much of the remainder is shipped to China for smelting. Antimony resources are unevenly distributed around the world. China has the bulk of the world’s identified resources; other countries that have identified antimony resources include Bolivia, Canada, Mexico, Russia, South Africa, Tajikistan, and Turkey. Resources in the United States are located mainly in Alaska, Idaho, Montana, and Nevada. The most significant antimony mineral deposits occur in geologic environments with a thick sequence of siliciclastic sedimentary rocks in areas with significant fault and fracture systems. The most common antimony ore mineral is stibnite (Sb2 S3 ), but more than 100 other minerals also contain antimony. The presence of antimony in surface waters and groundwaters results primarily from rock weathering, soil runoff, and anthropogenic sources. Global emissions of antimony to the atmosphere average 6,100 metric tons per year. Empirical data suggest that the acid-generating potential of antimony mine waste is low.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802C","isbn":"978-1-4113-3991-0","usgsCitation":"Seal, R.R., II, Schulz, K.J., and DeYoung, J.H., Jr., with contributions from David M. Sutphin, Lawrence J. Drew, James F. Carlin, Jr., and Byron R. Berger, 2017, Antimony, chap. C of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. C1–C17, https://doi.org/10.3133/pp1802C.","productDescription":"vii, 17 p.","numberOfPages":"30","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-078901","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":352475,"rank":3,"type":{"id":12,"text":"Errata"},"url":"https://pubs.usgs.gov/pp/1802/pp1802_erratum-march132018.txt","text":"Erratum","size":"1 KB","linkFileType":{"id":2,"text":"txt"}},{"id":339520,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/c/coverthb1.jpg"},{"id":339513,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/c/pp1802c.pdf","text":"Report","size":"7.05 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 C"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
The rare-earth elements (REEs) are 15 elements that range in atomic number from 57 (lanthanum) to 71 (lutetium); they are commonly referred to as the “lanthanides.” Yttrium (atomic number 39) is also commonly regarded as an REE because it shares chemical and physical similarities and has affinities with the lanthanides. Although REEs are not rare in terms of average crustal abundance, the concentrated deposits of REEs are limited in number.
Because of their unusual physical and chemical properties, the REEs have diverse defense, energy, industrial, and military technology applications. The glass industry is the leading consumer of REE raw materials, which are used for glass polishing and as additives that provide color and special optical properties to the glass. Lanthanum-based catalysts are used in petroleum refining, and cerium-based catalysts are used in automotive catalytic converters. The use of REEs in magnets is a rapidly increasing application. Neodymium-iron-boron magnets, which are the strongest known type of magnets, are used when space and weight are restrictions. Nickel-metal hydride batteries use anodes made of a lanthanum-based alloys.
China, which has led the world production of REEs for decades, accounted for more than 90 percent of global production and supply, on average, during the past decade. Citing a need to retain its limited REE resources to meet domestic requirements as well as concerns about the environmental effects of mining, China began placing restrictions on the supply of REEs in 2010 through the imposition of quotas, licenses, and taxes. As a result, the global rare-earth industry has increased its stockpiling of REEs; explored for deposits outside of China; and promoted new efforts to conserve, recycle, and substitute for REEs. New mine production began at Mount Weld in Western Australia, and numerous other exploration and development projects noted in this chapter are ongoing throughout the world.
The REE-bearing minerals are diverse and often complex in composition. At least 245 individual REE-bearing minerals are recognized; they are mainly carbonates, fluorocarbonates, and hydroxylcarbonates (n = 42); oxides (n = 59); silicates (n = 85); and phosphates (n = 26).
Many of the world’s significant REE deposits occur in carbonatites, which are carbonate igneous rocks. The REEs also have a strong genetic association with alkaline magmatism. The systematic geologic and chemical processes that explain these observations are not well understood. Economic or potentially economic REE deposits have been found in (a) carbonatites, (b) peralkaline igneous systems, (c) magmatic magnetite-hematite bodies, (d) iron oxide-copper-gold (IOCG) deposits, (e) xenotime-monazite accumulations in mafic gneiss, (f) ion-absorption clay deposits, and (g) monazite-xenotime-bearing placer deposits. Carbonatites have been the world’s main source for the light REEs since the 1960s. Ion-adsorption clay deposits in southern China are the world’s primary source of the heavy REEs. Monazite-bearing placer deposits were important sources of REEs before the mid-1960s and may be again in the future. In recent years, REEs have been produced from large carbonatite bodies mined at the Mountain Pass deposit in California and, in China, at the Bayan Obo deposit in Nei Mongol Autonomous Region, the Maoniuping deposit in Sichuan Province, the Daluxiang deposit in Sichuan Province, and the Weishan deposit in Anhui Province. Alkaline igneous complexes have recently been targeted for exploration because of their enrichments in the heavy REEs.
Information relevant to the environmental aspects of REE mining is limited. Little is known about the aquatic toxicity of REEs. The United States lacks drinking water standards for REEs. The concentrations of REEs in environmental media are influenced by their low abundances in crustal rocks and their limited solubility in most groundwaters and surface waters. The scarcity of sulfide minerals, including pyrite, minimizes or eliminates concerns about acid-mine drainage for carbonatite-hosted deposits and alkaline-intrusion-related REE deposits. For now, insights into environmental responses of REE mine wastes must rely on predictive models.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802O","isbn":"978-1-4113-3991-0","usgsCitation":"Van Gosen, B.S., Verplanck, P.L., Seal, R.R., II, Long, K.R., and Gambogi, Joseph, 2017, Rare-earth elements, chap. O of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. O1–O31, https://doi.org/10.3133/pp1802O.","productDescription":"viii, 31 p.","numberOfPages":"44","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-050900","costCenters":[{"id":171,"text":"Central Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334627,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/o/pp1802o.pdf","text":"Report","size":"4.50 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 O"},{"id":334626,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/o/coverthb1.jpg"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Fluorine compounds are essential in numerous chemical and manufacturing processes. Fluorspar is the commercial name for fluorite (isometric CaF2), which is the only fluorine mineral that is mined on a large scale. Fluorspar is used directly as a fluxing material and as an additive in different manufacturing processes. It is the source of fluorine in the production of hydrogen fluoride or hydrofluoric acid, which is used as the feedstock for numerous organic and inorganic chemical compounds.
The United States was the world’s leading producer of fluorspar until the mid-1950s. In the mid-1970s, the U.S. fluorspar mining industry began to decline because of foreign competition. By 1982, there was essentially only a single U.S. producer left, and that company ceased mining in 1996. Consumption of fluorspar in the United States peaked in the early 1970s, which was also the peak period of U.S. steel production. Since then, U.S. fluorspar consumption has decreased substantially; the United States has nonetheless increased its imports of downstream fluorine compounds, such as, in order of tonnage imported, hydrofluoric acid, aluminum fluoride, and cryolite. This combination of no U.S. production (until recently) and high levels of consumption has made the United States the world’s leading fluorspar-importing country, in all its various forms.
The number of fluorspar-exporting countries has decreased substantially in recent decades, and, as a result, the United States has become dependent on just a few countries to supply its needs. In 2013, the United States imported the majority of its fluorspar from three countries, which were, in descending order of the amount imported, Mexico, China, and South Africa.
Geologically, in igneous systems, fluorine is one of a number of elements that are “incompatible.” These incompatible elements become concentrated in the residual magma while the common silicates crystallize upon magma ascent and cooling, leading to relatively high fluorine concentrations in the more evolved or differentiated igneous rocks and in hydrothermal deposits associated with those evolved igneous rocks. In sedimentary rocks, fluorine’s highest concentrations are found in phosphorites because fluorine substitutes for hydroxyl ions in apatite, which leads to fluorine concentrations of, typically, from 2 to 4 weight percent in phosphorites. Because of the presence of fluorine, phosphate fertilizer manufacturers can produce a fluorosilicic acid byproduct. Most deposits mined for fluorine are hydrothermal, however, and consist of fluorine minerals that precipitated from hot water. Magmatic brines and brines from deep within sedimentary basins that have high concentrations of dissolved fluoride are the mineralizing fluids for various types of hydrothermal fluorspar deposits. Relatively dilute hydrothermal fluids that formed in some volcanic rocks can also transport sufficient fluoride to form a high-grade fluorspar deposit. Fluorite has low solubility in a common range of hydrothermal temperatures, particularly from about 160 degrees Celsius (°C) down to 60 °C. The increasing fluorite solubility below 60 °C partly explains why some water with exceptionally high levels of dissolved fluorine are found even at ambient temperatures in evaporitic lake basins in some East African Rift valleys in Kenya and Tanzania. The geologic conditions that led to the high concentrations there are known to exist in a number of other places in the world as well, including, perhaps, places in the Basin and Range province of the United States.
Eight minerals or mineral groups have sufficient fluorine in their structures to be considered as possible ores of the element; they are bastnaesite (also spelled bastnäsite; and other fluorocarbonates), cryolite, sellaite, villiaumite, fluorite, fluorapatite (in phosphorites), various phyllosilicates, and topaz. Fluorite is currently the only mineral that is mined for fluorine, and nomineral except fluorite is likely to become a source of commercially produced fluorine as a primary product as long as supplies from relatively thick and high-grade fluorite deposits continue to be available.
At least seven classes (which include one subclass) of hydrothermal fluorite deposits are recognized; they are classified according to their tectonic and (or) magmatic settings, as follows: (1) carbonatite-related fluorspar deposits; (2) alkaline-intrusion-related fluorspar deposits; (3) alkaline-volcanic-related epithermal fluorspar deposits; (4) Mississippi Valley-type fluorspar deposits (and a subclass of salt-related carbonate-hosted fluorspar deposits); (5) fluorspar deposits related to strongly differentiated granites; (6) subalkaline-volcanic-related epithermal fluospar deposits; and (7) fluorspar deposits that appear to be conformable within tuffaceous limy lacustrine sediments. An eighth class (not hydrothermal) is that of fluorspar deposits concentrated in soils and weathered zones; that is, residual fluorspar deposits. Generally, fluorspar deposits related to strongly differentiated granites have larger tonnages and lower grades than carbonatite-related fluorspar deposits, which, in turn, have larger tonnages and lower grades than fluorspar vein deposits from various other classes.
The United States has a few identified resources of fluorspar, most notably the Klondike II property in the Illinois- Kentucky fluorspar district located about 8 kilometers southwest of Salem, Kentucky, which has a large vein that contains at least 1.6 million metric tons at a grade of 60 percent CaF2 (Feytis, 2009). Additional fluorspar resources of lower grade but larger tonnage have been identified at Hicks Dome in the Illinois-Kentucky fluorspar district and at Lost River near the western tip of the Seward Peninsula in Alaska, along with a couple of dozen smaller, higher grade resources.
Internationally, new mines that either opened before the beginning of 2013 or were scheduled to open soon after that time include the Nui Phao tungsten-fluorspar-bismuth-copper-gold deposit in northern Vietnam; the St. Lawrence project in Newfoundland, Canada, which is located in a well-known fluorspar district; the Bamianshan deposit, which is related to a strongly differentiated granite in northwestern Zhejiang Province, China, near some of that Province’s large, subalkaline-volcanic-related epithermal veins; and the Nokeng project in South Africa, which is also related to a strongly differentiated granite. Other deposits in northwestern Australia, Nevada (United States), Norway, South Africa, and Sweden have been identified and could be put into production within just a few years.
Among undiscovered resources, an interesting possibility might be to produce a fluorine product from evaporitic, high-fluorine, high-pH sodium-carbonate brines like Lake Magadi (Kenya) and Lake Natron (Tanzania) in Africa’s Eastern Rift Valley. In addition, apparently conformable fluorspar deposits in tuffaceous limy lacustrine sediments, such as those in Italy, are likely to occur in similar young alkalic volcanic settings elsewhere in the world.
Modern geophysical and geochemical exploration techniques have typically not been brought to bear in exploration for new fluorspar deposits, although such techniques are likely to be used in future exploration. The tendency for fluorine to dissolve in significant concentrations in water at low temperature allows both surface water and groundwater to be used as sampling media in geochemical exploration. Evolved granite-related fluorspar deposits may be particularly susceptible to geophysical exploration methods because crystalline rocks that form a basement to sedimentary sections can be approximately defined with gravity and magnetic methods, and magnetite-bearing skarns can be directly detected with magnetic surveys.
Environmental considerations of fluorine mining focus especially on drinking water, where high fluorine concentrations can lead to tooth decay; dental and skeletal fluorosis; and bone and cartilage conditions, including genu valgum, which is the crippling bone deformity more commonly known as knock knee. Trace amounts of other elements in fluorspar ores are a concern at some deposits; for example, high beryllium concentrations in alkaline-volcanic-related epithermal deposits or high cadmium concentrations associated with Mississippi Valley-type and salt-related carbonate-hosted fluorspar deposits.
Future research might include testing whether fluorine can be extracted economically from high-pH, sodium-carbonate brines and exploring for new occurrences of apparently conformable fluorspar deposits in tuffaceous limy lacustrine sediments outside of the Latium Region of Italy. Other promising new areas of research could be studies of fluorspar deposit fluid inclusion compositions by quadrupole mass spectrometry, by noble gas mass spectrometry on irradiated fluid inclusions, or by chlorine isotopes, while also measuring the chemistry of the same fluid inclusions either by bulk crush-and-leach methods or by laser ablation-inductively coupled plasma mass spectrometry. Advanced studies of fluid inclusion chemistry could be applied beneficially to some of the enigmatic large epithermal fluorspar veins at various places in the world, where they might determine those deposits’ possible relationships to igneous intrusions, or to dissolved salt, or to heated meteoric water in volcanic sections, or perhaps to all three. This knowledge could help focus new exploration.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802G","isbn":"978-1-4113-3991-0","usgsCitation":"Hayes, T.S., Miller, M.M., Orris, G.J., and Piatak, N.M., 2017, Fluorine, chap. G of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. G1–G80, https://doi.org/10.3133/pp1802G.","productDescription":"viii, 80 p.","numberOfPages":"92","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-049496","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true},{"id":312,"text":"Geology, Minerals, Energy, and Geophysics Science Center","active":true,"usgs":true}],"links":[{"id":334567,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/g/coverthb1.jpg"},{"id":334568,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/g/pp1802g.pdf","text":"Report","size":"12.6 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 F"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Throughout most of human history, environmental stewardship during mining has not been a priority partly because of the lack of applicable laws and regulations and partly because of ignorance about the effects that mining can have on the environment. In the United States, the National Environmental Policy Act of 1969, in conjunction with related laws, codified a more modern approach to mining, including the responsibility for environmental stewardship, and provided a framework for incorporating environmental protection into mine planning. Today, similar frameworks are in place in the other developed countries of the world, and international mining companies generally follow similar procedures wherever they work in the world. The regulatory guidance has fostered an international effort among all stakeholders to identify best practices for environmental stewardship.
The modern approach to mining using best practices involves the following: (a) establishment of a pre-mining baseline from which to monitor environmental effects during mining and help establish geologically reasonable closure goals; (b) identification of environmental risks related to mining through standardized approaches; and (c) formulation of an environmental closure plan before the start of mining. A key aspect of identifying the environmental risks and mitigating those risks is understanding how the risks vary from one deposit type to another—a concept that forms the basis for geoenvironmental mineral-deposit models.
Accompanying the quest for best practices is the goal of making mining sustainable into the future. Sustainable mine development is generally considered to be development that meets the needs of the present generation without compromising the ability of future generations to meet their own needs. The concept extends beyond the availability of nonrenewable mineral commodities and includes the environmental and social effects of mine development.
Global population growth, meanwhile, has decreased the percentage of inhabitable land available to support society’s material needs. Presently, the land area available to supply the mineral resources, energy resources, water, food, shelter, and waste disposal needs of all Earth’s inhabitants is estimated to be 135 square meters per person. Continued global population growth will only increase the challenges of sustainable mining.
Current trends in mining are also expected to lead to new environmental challenges in the future, among which are mine-waste management issues related to mining larger deposits for lower ore grade; water-management issues related to both the mining of larger deposits and the changes in precipitation brought about by climate change; and greenhouse gas issues related to reducing the carbon footprint of larger, more energy-intensive mining operations.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802B","isbn":"978-1-4113-3991-0","usgsCitation":"Seal, R.R., II, Piatak, N.M., Kimball, B.E., and Hammarstrom, J.M., 2017, Environmental considerations related to mining of nonfuel minerals, chap. B of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. B1–B16, https://doi.org/10.3133/pp1802B.","productDescription":"vii, 16 p.","numberOfPages":"28","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-056555","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334557,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/b/coverthb1.jpg"},{"id":334560,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/b/pp1802b.pdf","text":"Report","size":"2.20 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 B"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Titanium is a mineral commodity that is essential to the smooth functioning of modern industrial economies. Most of the titanium produced is refined into titanium dioxide, which has a high refractive index and is thus able to impart a durable white color to paint, paper, plastic, rubber, and wallboard. Because of their high strength-to-weight ratio and corrosion resistance, titanium metal and titanium metal alloys are used in the aerospace industry as well as for welding rod coatings, biological implants, and consumer goods.
Ilmenite and rutile are currently the principal titanium-bearing ore minerals, although other minerals, including anatase, perovskite, and titanomagnetite, could have economic importance in the future. Ilmenite is currently being mined from two large magmatic deposits hosted in rocks of Proterozoic-age anorthosite plutonic suites. Most rutile and nearly one-half of the ilmenite produced are from heavy-mineral alluvial, fluvial, and eolian deposits. Titanium-bearing minerals occur in diverse geologic settings, but many of the known deposits are currently subeconomic for titanium because of complications related to the mineralogy or because of the presence of trace contaminants that can compromise the pigment production process.
Global production of titanium minerals is currently dominated by Australia, Canada, Norway, and South Africa; additional amounts are produced in Brazil, India, Madagascar, Mozambique, Sierra Leone, and Sri Lanka. The United States accounts for about 4 percent of the total world production of titanium minerals and is heavily dependent on imports of titanium mineral concentrates to meet its domestic needs.
Titanium occurs only in silicate or oxide minerals and never in sulfide minerals. Environmental considerations for titanium mining are related to waste rock disposal and the impact of trace constituents on water quality. Because titanium is generally inert in the environment, human health risks from titanium and titanium mining are minimal; however, the processes required to extract titanium from titanium feedstock can produce industrial waste.
","largerWorkType":{"id":18,"text":"Report"},"largerWorkTitle":"Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply","largerWorkSubtype":{"id":5,"text":"USGS Numbered Series"},"language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802T","isbn":"978-1-4113-3991-0","usgsCitation":"Woodruff, L.G., Bedinger, G.M., and Piatak, N.M., 2017, Titanium, chap. T of Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, p. T1–T23, https://doi.org/10.3133/pp1802T.","productDescription":"viii, 23 p.","numberOfPages":"36","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-045879","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":334850,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/t/coverthb1.jpg"},{"id":334851,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/t/pp1802t.pdf","text":"Report","size":"10.7 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802 T"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
https://minerals.usgs.gov
Mineral commodities are vital for economic growth, improving the quality of life, providing for national defense, and the overall functioning of modern society. Minerals are being used in larger quantities than ever before and in an increasingly diverse range of applications. With the increasing demand for a considerably more diverse suite of mineral commodities has come renewed recognition that competition and conflict over mineral resources can pose significant risks to the manufacturing industries that depend on them. In addition, production of many mineral commodities has become concentrated in relatively few countries (for example, tungsten, rare-earth elements, and antimony in China; niobium in Brazil; and platinum-group elements in South Africa and Russia), thus increasing the risk for supply disruption owing to political, social, or other factors. At the same time, an increasing awareness of and sensitivity to potential environmental and health issues caused by the mining and processing of many mineral commodities may place additional restrictions on mineral supplies. These factors have led a number of Governments, including the Government of the United States, to attempt to identify those mineral commodities that are viewed as most “critical” to the national economy and (or) security if supplies should be curtailed.
This book presents resource and geologic information on the following 23 mineral commodities currently among those viewed as important to the national economy and national security of the United States: antimony (Sb), barite (barium, Ba), beryllium (Be), cobalt (Co), fluorite or fluorspar (fluorine, F), gallium (Ga), germanium (Ge), graphite (carbon, C), hafnium (Hf), indium (In), lithium (Li), manganese (Mn), niobium (Nb), platinum-group elements (PGE), rare-earth elements (REE), rhenium (Re), selenium (Se), tantalum (Ta), tellurium (Te), tin (Sn), titanium (Ti), vanadium (V), and zirconium (Zr). For a number of these commodities—for example, graphite, manganese, niobium, and tantalum—the United States is currently wholly dependent on imports to meet its needs. The first two chapters (A and B) deal with general information pertinent to the study of mineral resources. Chapters C through V describe individual mineral commodities and include an overview of current uses of the commodity, identified resources and their distribution nationally and globally, the state of current geologic knowledge, the potential for finding additional deposits nationally and globally, and geoenvironmental issues that may be related to the production and uses of the commodity. These chapters are updates of the commodity chapters published in 1973 in U.S. Geological Survey Professional Paper 820, “United States Mineral Resources.”
","language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/pp1802","isbn":"978-1-4113-3991-0","usgsCitation":"Schulz, K.J., DeYoung, J.H., Jr., Seal, R.R., II, and Bradley, D.C., eds., 2017, Critical mineral resources of the United States—Economic and environmental geology and prospects for future supply: U.S. Geological Survey Professional Paper 1802, 797 p., https://doi.org/10.3133/pp1802.","productDescription":"Report: 862 p.; Data Release","numberOfPages":"862","onlineOnly":"N","additionalOnlineFiles":"N","ipdsId":"IP-069563","costCenters":[{"id":245,"text":"Eastern Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":350071,"rank":5,"type":{"id":22,"text":"Related Work"},"url":"https://mrdata.usgs.gov/pp1802/ ","text":"- Global Distribution of Selected Mines, Deposits, and Districts of Critical Minerals","linkFileType":{"id":5,"text":"html"},"description":"Global distribution of selected mines, deposits, and districts of critical minerals"},{"id":336929,"rank":2,"type":{"id":8,"text":"Cover"},"url":"https://pubs.usgs.gov/pp/1802/pp1802_frontbackcovers.pdf","text":"Front and Back Covers","size":"1.23 MB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802"},{"id":352473,"rank":7,"type":{"id":12,"text":"Errata"},"url":"https://pubs.usgs.gov/pp/1802/pp1802_erratum-march132018.txt","text":"Erratum","size":"1 KB","linkFileType":{"id":2,"text":"txt"}},{"id":336933,"rank":3,"type":{"id":2,"text":"Additional Report Piece"},"url":"https://pubs.usgs.gov/pp/1802/cover/pp1802frontmatter.pdf","text":"Professional Paper 1802 - Front Matter","size":"326 KB","linkFileType":{"id":1,"text":"pdf"},"description":"PP 1802","linkHelpText":" - Front Matter"},{"id":336928,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/pp/1802/coverthb.jpg"},{"id":350094,"rank":6,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/pp/1802/pp1802_entirebook.pdf","text":"Report (Entire Book)","size":"148 MB","linkFileType":{"id":1,"text":"pdf"}},{"id":349464,"rank":4,"type":{"id":30,"text":"Data Release"},"url":"https://doi.org/10.5066/F7GH9GQR","text":"USGS data release","description":"USGS data release","linkHelpText":"Global Distribution of Selected Mines, Deposits, and Districts of Critical Minerals"}],"contact":"Mineral Resources Program Coordinator
U.S. Geological Survey
913 National Center
Reston, VA 20192
Email: minerals@usgs.gov
http://minerals.usgs.gov
Solid organic matter (OM) plays an essential role in the generation, migration, storage, and production of hydrocarbons from economically important shale rock formations. Electron microscopy images have documented spatial heterogeneity in the porosity of OM at nanoscale, and bulk spectroscopy measurements have documented large variation in the chemical composition of OM during petroleum generation. However, information regarding the heterogeneity of OM chemical composition at the nanoscale has been lacking. Here we demonstrate the first application of atomic force microscopy-based infrared spectroscopy (AFM-IR) to measure the chemical and mechanical heterogeneity of OM in shale at the nanoscale, orders of magnitude finer than achievable by traditional chemical imaging tools such as infrared microscopy. We present a combination of optical microscopy and AFM-IR imaging to characterize OM heterogeneity in an artificially matured series of New Albany Shales. The results document the evolution of individual organic macerals with maturation, providing a microscopic picture of the heterogeneous process of petroleum generation.
The Yellowstone Plateau is one of the largest manifestations of silicic volcanism on Earth, and marks the youngest focus of magmatism associated with the Yellowstone Hot Spot. The earliest products of Yellowstone Hot Spot volcanism are from ~17 million years ago, but may be as old as ~32 Ma, and include contemporaneous eruption of voluminous mafic and silicic magmas, which are mostly located in the region of northwestern Nevada and southeastern Oregon. Since 17 Ma, the main locus of Yellowstone Hot Spot volcanism has migrated northeastward producing numerous silicic caldera complexes that generally remain active for ~2–4 million years, with the present-day focus being the Yellowstone Plateau. Northeastward migration of volcanism associated with the Yellowstone Hot Spot resulted in the formation of the Snake River Plain, a low relief physiographic feature extending ~750 kilometers from northern Nevada to eastern Idaho. Most of the silicic volcanic centers along the Snake River Plain have been inundated by younger basalt volcanism, but many of their ignimbrites and lava flows are exposed in the extended regions at the margins of the Snake River Plain.
","language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/sir20175022Q","usgsCitation":"Vazquez, J., Stelten, M., Bindeman, I., and Cooper, K., 2017, A field trip guide to the petrology of Quaternary volcanism on the Yellowstone Plateau: U.S. Geological Survey Scientific Investigations Report 2017–5022–Q, 68 p., https://doi.org/10.3133/sir20175022q.","productDescription":"x, 68 p.","numberOfPages":"82","onlineOnly":"Y","ipdsId":"IP-078151","costCenters":[{"id":617,"text":"Volcano Science Center","active":true,"usgs":true}],"links":[{"id":350111,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/sir/2017/5022/q/coverthb.jpg"},{"id":350112,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/sir/2017/5022/q/sir20175022q_.pdf","text":"Report","size":"9 MB","linkFileType":{"id":1,"text":"pdf"},"description":"SIR 2017-5022-Q"}],"country":"United States","state":"Wyoming","otherGeospatial":"Yellowstone National Park","geographicExtents":"{\n \"type\": \"FeatureCollection\",\n \"features\": [\n {\n \"type\": \"Feature\",\n \"properties\": {},\n \"geometry\": {\n \"type\": \"Polygon\",\n \"coordinates\": [\n [\n [\n -111.05529785156249,\n 44.04811573082351\n ],\n [\n -110.19012451171875,\n 44.04811573082351\n ],\n [\n -110.19012451171875,\n 45.00170912094224\n ],\n [\n -111.05529785156249,\n 45.00170912094224\n ],\n [\n -111.05529785156249,\n 44.04811573082351\n ]\n ]\n ]\n }\n }\n ]\n}","contact":"Volcano Science Center - Menlo Park
U.S. Geological Survey
345 Middlefield Road, MS 910
Menlo Park, CA 94025
This report describes the discovery and geology of two near-surface uranium deposits within calcareous lacustrine strata of Pleistocene age in west Texas, United States. Calcrete uranium deposits have not been previously reported in the United States. The west Texas uranium deposits share characteristics with some calcrete uranium deposits in Western Australia—uranium-vanadium minerals hosted by nonpedogenic calcretes deposited in saline lacustrine environments.
In the mid-1970s, Kerr-McGee Corporation conducted a regional uranium exploration program in the Southern High Plains province of the United States, which led to the discovery of two shallow uranium deposits (that were not publicly reported). With extensive drilling, Kerr-McGee delineated one deposit of about 2.1 million metric tons of ore with an average grade of 0.037 percent U3O8 and another deposit of about 0.93 million metric tons of ore averaging 0.047 percent U3O8.
The west-Texas calcrete uranium-vanadium deposits occur in calcareous, fine-grained sediments interpreted to be deposited in saline lakes formed during dry interglacial periods of the Pleistocene. The lakes were associated with drainages upstream of a large Pleistocene lake. Age determinations of tephra in strata adjacent to one deposit indicate the host strata is middle Pleistocene in age.
Examination of the uranium-vanadium mineralization by scanning-electron microscopy indicated at least two generations of uranium-vanadium deposition in the lacustrine strata identified as carnotite and a strontium-uranium-vanadium mineral. Preliminary uranium-series results indicate a two-component system in the host calcrete, with early lacustrine carbonate that was deposited (or recrystallized) about 190 kilo-annum, followed much later by carnotite-rich crusts and strontium-uranium-vanadium mineralization in the Holocene (about 5 kilo-annum). Differences in initial 234U/238U activity ratios indicate two separate, distinct fluid sources.
","language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/sir20175134","usgsCitation":"Van Gosen, B.S., and Hall, S.M., 2017, The discovery and character of Pleistocene calcrete uranium deposits in the Southern High Plains of west Texas, United States: U.S. Geological Survey Scientific Investigations Report 2017–5134, 27 p., https://doi.org/10.3133/sir20175134.","productDescription":"vi, 27 p.","numberOfPages":"36","onlineOnly":"Y","ipdsId":"IP-088741","costCenters":[{"id":171,"text":"Central Mineral and Environmental Resources Science Center","active":true,"usgs":true}],"links":[{"id":350099,"rank":3,"type":{"id":22,"text":"Related Work"},"url":"https://doi.org/10.3133/fs20173078","text":"U.S. Geological Survey Fact Sheet: ","linkHelpText":"Assessment of undiscovered resources in calcrete uranium deposits, Southern High Plains region of Texas, New Mexico, and Oklahoma, 2017"},{"id":350088,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/sir/2017/5134/coverthb.jpg"},{"id":350089,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/sir/2017/5134/sir20175134.pdf","text":"Report","size":"23.0 MB","linkFileType":{"id":1,"text":"pdf"},"description":"SIR 2017–5134"}],"country":"United States","state":"Texas","otherGeospatial":"Southern High Plains","geographicExtents":"{\n \"type\": \"FeatureCollection\",\n \"features\": [\n {\n \"type\": \"Feature\",\n \"properties\": {},\n \"geometry\": {\n \"type\": \"Polygon\",\n \"coordinates\": [\n [\n [\n -103.0517578125,\n 31.90087807776307\n ],\n [\n -100.8270263671875,\n 31.90087807776307\n ],\n [\n -100.8270263671875,\n 33.61919376817004\n ],\n [\n -103.0517578125,\n 33.61919376817004\n ],\n [\n -103.0517578125,\n 31.90087807776307\n ]\n ]\n ]\n }\n }\n ]\n}","contact":"Director, Central Mineral and Environmental Resources Science Center
U.S. Geological Survey
Box 25046, MS 973
Denver, CO 80225
Tsala Apopka Lake is a complex system of lakes and wetlands, with intervening uplands, located in Citrus County in west-central Florida. It is located within the 2,100 square mile watershed of the Withlacoochee River, which drains north and northwest towards the Gulf of Mexico. The lake system is managed by the Southwest Florida Water Management District as three distinct “pools,” which from upstream to downstream are referred to as the Floral City Pool, Inverness Pool, and Hernando Pool. Each pool contains a mixture of deep-water lakes that remain wet year round, ephemeral (seasonal) ponds and wetlands, and dry uplands. Many of the major deep-water lakes are interconnected by canals. Flow from the Withlacoochee River, when conditions allow, can be diverted into the lake system. Flow thorough the canals can be used to control the distribution of water between the three pools. Flow in the canals is controlled using structures, such as gates and weirs.
Hydrogeologic units in the study area include a surficial aquifer consisting of Quaternary-age sediments, a discontinuous intermediate confining unit consisting of Miocene- and Pliocene-age sediments, and the underlying Upper Floridan aquifer, which consists of Eocene- and Oligocene-age carbonates. The fine-grained quartz sands that constitute the surficial aquifer are generally thin, typically less than 25 feet thick, within the vicinity of Tsala Apopka Lake. A thin, discontinuous, sandy clay layer forms the intermediate confining unit. The Upper Floridan aquifer is generally unconfined in the vicinity of Tsala Apopka Lake because the intermediate confining unit is discontinuous and breached by numerous karst features. In the study area, the Upper Floridan aquifer includes the upper Avon Park Formation and Ocala Limestone. The Ocala Limestone is the primary source of drinking water and spring flow in the area.
The objectives of this study are to document the interaction of Tsala Apopka Lake, the surficial aquifer, and the Upper Floridan aquifer; and to estimate an annual water budget for each pool and for the entire lake system for 2004–12. The hydrologic interactions were evaluated using hydraulic head and geochemical data. Geochemical data, including major ion, isotope, and age-tracer data, were used to evaluate sources of water and to distinguish flow paths. Hydrologic connection of the surficial environment (lakes, ponds, wetlands, and the surficial aquifer) was quantified on the basis of a conceptualized annual water-budget model. The model included the change in surface water and groundwater storage, precipitation, evapotranspiration, surface-water inflow and outflow, and net groundwater exchange with the underlying Upper Floridan aquifer. The control volume for each pool extended to the base of the surficial aquifer and covered an area defined to exceed the maximum inundated area for each pool during 2004–12 by 0.5 foot. Net groundwater flow was computed as a lumped value and was either positive or negative, with a negative value indicating downward or lateral leakage from the control volume and a positive value indicating upward leakage to the control volume.
The annual water budget for Tsala Apopka Lake was calculated using a combination of field observations and remotely sensed data for each of three pools and for the composite three pool area. A digital elevation model at a 5-foot grid spacing and bathymetric survey data were used to define the land-surface elevation and volume of each pool and to calculate the changes in inundated area with change in lake stage. Continuous lake-stage and groundwater-level data were used to define the change in storage for each pool. The rainfall data used in the water-budget calculations were based on daily radar reflectance data and measured rainfall from weather stations. Evapotranspiration was computed as a function of reference evapotranspiration, adjusted to actual evapotranspiration using a monthly land-cover coefficient (based on evapotranspiration measurements at stations located in representative landscapes). Surface-water inflows and outflows were determined using stage data collected at a series of streamgages installed primarily at the water-control structures. Discharge was measured under varying flow regimes and ratings were developed for the water-control structures. The discharge data collected during the study period were used to calibrate a surface-water flow model for 2004–12. Flows predicted by the model were used in the water-budget analysis. Net groundwater flow was determined as the residual term in the water-budget equation.
The results of the water-budget analysis indicate that rainfall was the largest input of water to Tsala Apopka Lake, whereas evapotranspiration was the largest output. For the 2004–12 analysis period, surface-water inflow accounted for 11 percent of the inputs, net groundwater inflow accounted for 1 percent of inputs (annual periods with positive net groundwater flow were included as inputs, while annual periods with negative net groundwater flow were counted as outputs), and rainfall accounted for the remaining 88 percent. For the same period, the outputs consisted of 2 percent surface-water outflow, 12 percent net groundwater outflow, and 86 percent evapotranspiration. Net groundwater inflows and surface-water/groundwater storage were negligible during the water-budget period but could be important components of the budget in individual years.
The net groundwater flow was negative (downward) for 8 out of the 9 years modeled (2004–12), indicating that the Tsala Apopka Lake study area was primarily a recharge area for the underlying Upper Floridan aquifer during this time period. Groundwater-level elevation in paired wells (adjacent wells completed in the surficial aquifer and Upper Floridan aquifer) typically was higher in the surficial aquifer than the Upper Floridan aquifer. However, hydraulic head data indicate that the surficial aquifer often has discharge potential to the surface-water system, especially in the low lying areas near the major lakes. Surficial-aquifer water levels were often higher than lake stages, especially during wet periods, which is likely an indication of aquifer-to-lake seepage in these areas. East of the major lakes, hydraulic head data were nearly equal in the surficial aquifer and Upper Floridan aquifer, which is an indication that the Upper Floridan aquifer is unconfined. Based on deuterium and oxygen stable isotope data collected in December 2011 and December 2012, there was no evidence of recharge to the Upper Floridan aquifer from the wetlands east of the major lakes; aquifer isotopic ratios did not indicate an enriched source, which is typical of lake and wetland sources. West of the major lakes, there was evidence of enriched isotopic ratios in water samples from the Upper Floridan aquifer. Differences in hydraulic head at paired wells in the surficial aquifer and Upper Floridan aquifer indicated that the surficial aquifer has the potential to recharge the Upper Floridan aquifer in the western part of the pools and west of the major lakes.
","language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/sir20175132","collaboration":"Prepared in cooperation with the Southwest Florida Water Management District","usgsCitation":"McBride, W.S., Metz, P.A., Ryan, P.J., Fulkerson, Mark, and Downing, H.C., 2017, Groundwater levels, geochemistry, and water budget of the Tsala Apopka Lake system, west-central Florida, 2004–12: U.S. Geological Survey Scientific Investigations Report 2017–5132, 100 p., https://doi.org/10.3133/sir20175132.","productDescription":"xi, 100 p.","numberOfPages":"116","onlineOnly":"Y","ipdsId":"IP-059771","costCenters":[{"id":270,"text":"FLWSC-Tampa","active":true,"usgs":true}],"links":[{"id":350056,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/sir/2017/5132/sir20175132.pdf","text":"Report","size":"14.0 MB","linkFileType":{"id":1,"text":"pdf"},"description":"SIR 2017–5132"},{"id":350055,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/sir/2017/5132/coverthb.jpg"}],"country":"United States","state":"Florida","otherGeospatial":"Tsala Apopka Lake System","geographicExtents":"{\n \"type\": \"FeatureCollection\",\n \"features\": [\n {\n \"type\": \"Feature\",\n \"properties\": {},\n \"geometry\": {\n \"type\": \"Polygon\",\n \"coordinates\": [\n [\n [\n -82.452392578125,\n 28.66890107414433\n ],\n [\n -82.0520782470703,\n 28.66890107414433\n ],\n [\n -82.0520782470703,\n 29.00693934321682\n ],\n [\n -82.452392578125,\n 29.00693934321682\n ],\n [\n -82.452392578125,\n 28.66890107414433\n ]\n ]\n ]\n }\n }\n ]\n}","contact":"Director, Caribbean-Florida Water Science Center
U.S. Geological Survey
4446 Pet Lane, Suite 108
Lutz, FL 33559
Sequoia Scientific’s LISST-ABS is an acoustic backscatter sensor designed to measure suspended-sediment concentration at a point source. Three LISST-ABS were evaluated at the U.S. Geological Survey (USGS) Hydrologic Instrumentation Facility (HIF). Serial numbers 6010, 6039, and 6058 were assessed for accuracy in solutions with varying particle-size distributions and for the effect of temperature on sensor accuracy. Certified sediment samples composed of different ranges of particle size were purchased from Powder Technology Inc. These sediment samples were 30–80-micron (µm) Arizona Test Dust; less than 22-µm ISO 12103-1, A1 Ultrafine Test Dust; and 149-µm MIL-STD 810E Silica Dust. The sensor was able to accurately measure suspended-sediment concentration when calibrated with sediment of the same particle-size distribution as the measured. Overall testing demonstrated that sensors calibrated with finer sized sediments overdetect sediment concentrations with coarser sized sediments, and sensors calibrated with coarser sized sediments do not detect increases in sediment concentrations from small and fine sediments. These test results are not unexpected for an acoustic-backscatter device and stress the need for using accurate site-specific particle-size distributions during sensor calibration. When calibrated for ultrafine dust with a less than 22-µm particle size (silt) and with the Arizona Test Dust with a 30–80-µm range, the data from sensor 6039 were biased high when fractions of the coarser (149-µm) Silica Dust were added. Data from sensor 6058 showed similar results with an elevated response to coarser material when calibrated with a finer particle-size distribution and a lack of detection when subjected to finer particle-size sediment. Sensor 6010 was also tested for the effect of dissimilar particle size during the calibration and showed little effect. Subsequent testing revealed problems with this sensor, including an inadequate temperature compensation, making this data questionable. The sensor was replaced by Sequoia Scientific with serial number 6039. Results from the extended temperature testing showed proper temperature compensation for sensor 6039, and results from the dissimilar calibration/testing particle-size distribution closely corroborated the results from sensor 6058.
","language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/ofr20171154","usgsCitation":"Snazelle, T.T., 2017, Laboratory evaluation of the Sequoia Scientific LISST-ABS acoustic backscatter sediment sensor: U.S. Geological Survey Open-File Report 2017–1154, 21 p., https://doi.org/10.3133/ofr20171154.","productDescription":"Report: vii, 21 p.; Data; Metadata","numberOfPages":"34","onlineOnly":"Y","additionalOnlineFiles":"Y","ipdsId":"IP-083385","costCenters":[{"id":502,"text":"Office of Surface Water","active":true,"usgs":true}],"links":[{"id":350020,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/of/2017/1154/ofr20171154.pdf","text":"Report","size":"921 kB","linkFileType":{"id":1,"text":"pdf"},"description":"OFR 2017–1154"},{"id":350021,"rank":3,"type":{"id":16,"text":"Metadata"},"url":"https://www.sciencebase.gov/catalog/item/59ba9376e4b091459a563ba7","text":"Data and Metadata","linkHelpText":"HIF evaluation of LISST-ABS"},{"id":350019,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/of/2017/1154/coverthb.jpg"}],"contact":"Chief, Hydrologic Instrumentation Facility
U.S. Geological Survey
Building 2101
Stennis Space Center, MS 39529
We worked with managers in two focal areas to plan for the uncertain future by integrating quantitative climate change scenarios and simulation modeling into scenario planning exercises.
In our central North Dakota focal area, centered on Knife River Indian Villages National Historic Site, managers are concerned about how changes in flood severity and growing conditions for native and invasive plants may affect archaeological resources and cultural landscapes associated with the Knife and Missouri Rivers. Climate projections and hydrological modeling based on those projections indicate plausible changes in spring and summer soil moisture ranging from a 7 percent decrease to a 13 percent increase and maximum winter snowpack (important for spring flooding) changes ranging from a 13 percent decrease to a 47 percent increase. Facilitated discussions among managers and scientists exploring the implications of these different climate scenarios for resource management revealed potential conflicts between protecting archeological sites and fostering riparian cottonwood forests. The discussions also indicated the need to prioritize archeological sites for excavation or protection and culturally important plant species for intensive management attention.
In our southwestern South Dakota focal area, centered on Badlands National Park, managers are concerned about how changing climate will affect vegetation production, wildlife populations, and erosion of fossils, archeological artifacts, and roads. Climate scenarios explored by managers and scientists in this focal area ranged from a 13 percent decrease to a 33 percent increase in spring precipitation, which is critical to plant growth in the northern Great Plains region, and a slight decrease to a near doubling of intense rain events. Facilitated discussions in this focal area concluded that greater effort should be put into preparing for emergency protection, excavation, and preservation of exposed fossils or artifacts and revealed substantial opportunities for different agencies to learn from each other and cooperate on common management goals. Follow up quantitative simulation modeling of grassland dynamics helped quantify the degree of change expected in vegetation production under the wide range of climate scenarios and suggested that (a) low grazing rates could be adversely affecting vegetation composition in the national park and (b) understanding of the management practices needed to maintain desired vegetation conditions is incomplete.
","language":"English","publisher":"U.S. Geological Survey","publisherLocation":"Reston, VA","doi":"10.3133/ofr20171129","usgsCitation":"Symstad, A.J., Miller, B.W., Friedman, J.M., Fisichelli, N.A., Ray, A.J., Rowland, Erika, and Schuurman, G.W., 2017, Model-based scenario planning to inform climate change adaptation in the Northern Great Plains—Final report: U.S. Geological Survey Open-File Report 2017–1129, 22 p., https://doi.org/10.3133/ofr20171129.","productDescription":"Report: vii, 22 p.; Data Release","numberOfPages":"34","onlineOnly":"Y","ipdsId":"IP-089059","costCenters":[{"id":480,"text":"Northern Prairie Wildlife Research Center","active":true,"usgs":true}],"links":[{"id":348794,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/of/2017/1129/coverthb.jpg"},{"id":348795,"rank":2,"type":{"id":11,"text":"Document"},"url":"https://pubs.usgs.gov/of/2017/1129/ofr20171129.pdf","text":"Report","size":"2.63 MB","linkFileType":{"id":1,"text":"pdf"},"description":"OFR 2017–1129"},{"id":348796,"rank":3,"type":{"id":30,"text":"Data Release"},"url":"https://dx.doi.org/10.5066/F7T1524X","text":"USGS data release","linkHelpText":"State-and-transition simulation model of rangeland vegetation in southwest South Dakota (1969–2050)"}],"country":"United States","state":"Montana, Nebraska, North Dakota, South Dakota, Wyoming","geographicExtents":"{\n \"type\": \"FeatureCollection\",\n \"features\": [\n {\n \"type\": \"Feature\",\n \"properties\": {},\n \"geometry\": {\n \"type\": \"Polygon\",\n \"coordinates\": [\n [\n [\n -114,\n 41\n ],\n [\n -97,\n 41\n ],\n [\n -97,\n 49\n ],\n [\n -114,\n 49\n ],\n [\n -114,\n 41\n ]\n ]\n ]\n }\n }\n ]\n}","contact":"Director, Northern Prairie Wildlife Research Center
U.S. Geological Survey
8711 37th Street Southeast
Jamestown, North Dakota 58401