Critical Minerals in Subduction-related Magmatic-Hydrothermal Systems of the United States
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Acknowledgments
Numerous individuals provided information and insight on critical minerals in magmatic-hydrothermal, intrusion-related districts and deposits in Western States: Herb Duerr (Sunnyside, Arizona), Shaun Dykes (CuMo, Idaho), Bill Howald (Tonopah, Nevada), Buster Hunsaker and Mark Barton (McCullough Butte, Nevada), Hamish Martin (Resolution, Arizona), Eric Seedorff (copper-(molybdenum) deposits in Arizona), Ralph Stegen (Mo deposits), and Roger Steininger (Mo deposits). Drill hole analyses of the Pebble porphyry Cu-Mo deposit, Alaska, were provided by James Lang and Karen Kelley. Exploration and mining company websites and annual reports, 43-101 and technical reports, and archived records provided description of deposits and resources and, in some reports, quantification of critical minerals in them. Reviewers Jamie Brainard, Bob Seal, and Al Hofstra offered many relevant suggestions regarding content and presentation, most of which have been incorporated in some form.
Chemical Symbols
Al
aluminum
Sb
antimony
As
arsenic
Ba
barium
Be
beryllium
Bi
bismuth
Cd
cadmium
Ca
calcium
C
carbon
Ce
cerium
Cs
cesium
Cr
chromium
Co
cobalt
Cu
copper
Ga
gallium
Ge
germanium
Au
gold
Hf
hafnium
In
indium
Ir
iridium
Fe
iron
Pb
lead
La
lanthanum
Li
lithium
Mg
magnesium
Mn
manganese
Hg
mercury
Mo
molybdenum
Ni
nickel
Nb
niobium
Os
osmium
O
oxygen
Pd
palladium
P
phosphorus
Pt
platinum
K
potassium
Re
rhenium
Rh
rhodium
Rb
rubidium
Ru
ruthenium
Sc
scandium
Se
selenium
Ag
silver
Na
sodium
Sr
strontium
S
sulfur
Ta
tantalum
Te
tellurium
Tl
thallium
Th
thorium
Sn
tin
Ti
titanium
W
tungsten
U
uranium
V
vanadium
Zn
zinc
Zr
zirconium
Abstract
During the World War and Cold War eras (1910s–1990s), domestic consumption of numerous mineral commodities relied increasingly on imported supplies. Consumption reliance has since expanded to include 50 “critical minerals” (elements and mineral commodities) that are mostly to entirely imported and subject to curtailment by suppliers or supply chain disruption. New domestic supplies of critical minerals are being pursued by mining companies and by several federal departments and agencies. Information on domestic deposits and resources of critical minerals is being compiled by the U.S. Geological Survey Mineral Resources Program, which has organized investigations by mineral system, deposit type, and commodity.
Production, reserves, resources, and inventories of 21 critical minerals in domestic magmatic-hydrothermal deposits related to subduction-generated magmatism, and in tailings, slag, slimes, and electrolyte from copper concentrators, smelters, and refineries that processed some deposits, are largely restricted to Western States and Alaska. The critical mineral commodities Al, Sb, As, Bi, Co, fluorite, Ga, Ge, In, Mn, Ni, Nb, Pd, Pt, potash, Re, Ta, Te, Sn, W, and V are variably concentrated in porphyry/skarn copper-(molybdenum), skarn-replacement-vein (S-R-V) tungsten, polymetallic sulfide S-R-V intermediate sulfidation (IS), high-sulfidation gold-silver, low-sulfidation gold-silver, and lithocap alunite deposit types. These deposit types occur in porphyry copper-molybdenum-gold, alkalic porphyry, porphyry tin (granite related), and reduced intrusion-related mineral systems.
Production, reserves, and resources of Co, Ni, Nb, Pd, Pt, Ta, Sn, and V in subduction-related deposits in Western States are insignificant to small, mostly equivalent to months to a few years of recent annual domestic consumption (2016–2020). Significant inventories, equivalent to 2 or more years of consumption of aluminum, antimony, potash, and tungsten in unmined S-R-V tungsten, polymetallic sulfide S-R-V-IS, and lithocap alunite deposits vary from approximately 2 to 8 years. Several decades of consumption of arsenic, bismuth, fluorite, gallium, germanium, and indium exist in some polymetallic sulfide S-R-V-IS and lithocap alunite deposit types.
Based on concentrations of critical minerals in reserves, resources, drill holes, and deposit domains (ore types), and in captive refinery records, the largest domestic inventories of Sb, As, Bi, Re, and Te, and possibly Ga, Ge, In, Sn, and W, are in porphyry copper-molybdenum (Cu-Mo) deposits in Alaska, Idaho, Utah, and Arizona, and in interim products of processing porphyry Cu-Mo deposit ores for recovery of copper and molybdenum. Concentrations of critical minerals in archival specimens and sample collections, although somewhat biased by collection and conservation decisions and categorization, are broadly proportionate to those in reserves, resources, and drill holes. These concentrations imply significant inventories of some critical minerals in deposits for which production, resources, and refinery records are unavailable or incomplete.
Because of the large masses of ores mined and processed annually (hundreds of millions of metric tons) and in reserves and resources (hundreds of millions of metric tons to billions of metric tons), calculated inventories of critical minerals in porphyry Cu-Mo deposits are equivalent to decades and centuries of recent consumption. However, these inventories should not be considered consumable supplies without reserve definition and development of economically viable mining plans and recovery techniques. An expeditious strategy for elimination or reduction of import reliance is recovery, and improved recovery efficiency, of Sb, As, Bi, Re, and Te, and possibly Ga, Ge, In, Ni, Sn, Ti, and W; during concentration and refining of copper and molybdenum minerals in ores of operating porphyry Cu-Mo mines; and in unmined porphyry Cu-Mo resources. These chalcophile, siderophile, and lithophile critical minerals, often undetectable in ore, are concentrated (hundreds of parts per million to percents) in slimes and electrolyte during copper electrorefining or could be recovered, in part, during sulfide concentration and smelting. Other than rhenium (recovered during molybdenum refining) and tellurium, all have been routinely discarded.
Subsidization (for example, commodity price guarantees, tax credits, recovery technology development), political initiative, and (or) sustained market favorability could support new production of critical mineral commodities from subduction-related magmatic-hydrothermal deposits in Western States. In addition, insufficient domestic refining capacity could relegate the large inventories of critical minerals in porphyry Cu-Mo reserves and resources (for example, Pebble, Alaska; Resolution and Copper World [Rosemont], Arizona) to exportation in concentrates and importation insecurity, fortifying their present status.
Introduction
Critical minerals are mineral commodities “essential to the economic and national security of the United States” for which “the supply chain…is vulnerable to disruption” (Executive Office of the President, 2017; U.S. Department of Commerce, 2019). The term “critical minerals” refers to elements and minerals that are predominantly imported from various countries, some of which may discontinue exports to the United States because of political disputes or restricted availability of supplies. Presidential Executive Order No. 13817 (Executive Office of the President, 2017) and Secretarial Order No. 3359 (U.S. Department of the Interior, 2017) requested the U.S. Geological Survey (USGS) to determine possible domestic sources of critical minerals that could offset or eliminate import reliance. In 2018 a list of 35 critical minerals was released by the U.S. Department of the Interior (2018) (Fortier and others, 2018); 31 were designated import-reliant because imports provide more than 50 percent of annual domestic consumption. In 2021, zinc and nickel were added to the list, platinum group elements (PGE) and rare earth elements (REE) were individually listed, and several commodities were delisted (Nassar and Fortier, 2021), bringing the current list to 50 critical minerals. In response to the administration orders and first critical minerals list the USGS initiated and reorganized several projects, including the Earth Mineral Resources Initiative; the U.S. Mineral Deposit Database (USMIN) project; and the Systems Approach to Critical Minerals Inventory, Research, and Assessment project, to address domestic critical mineral supplies.
Domestic critical minerals covered in this report have been concentrated into deposits by magmatic and hydrothermal processes associated with plate subduction at convergent and transform plate margins of the Western United States. Subduction-related magmatism has been episodically active since the Early Triassic and is represented by granitic intrusions and volcanic fields in Arizona, California, Colorado, Idaho, Montana, Nevada, New Mexico, Oregon, Utah, and Washington. These igneous rocks mostly reflect partial melting of the mantle wedge by devolatilization of subducted oceanic crust and lesser pelagic sediments during convergent plate subduction. Basalt magmas generated by partial melting of mantle rocks intruded and partially melted lower and middle crust to form hybridized magmas. Hybridized magmas differentiated, buoyantly ascended, and erupted as andesites and felsic volcanic rocks or crystallized as granitic and porphyritic rocks in the upper crust. Production, resources, and inventories of metals and critical mineral commodities in the Western States were largely derived from, or occur in, deposits in granitic and porphyritic intrusions, in sedimentary rocks adjacent to intrusions, and in volcanic fields thought to overlie intrusions. Most deposits formed during the Late Cretaceous and Cenozoic. Those in westernmost States formed near the subduction zone during high-angle subduction and slab rollback whereas deposits in the Rocky Mountains States (Colorado, Montana, Wyoming, New Mexico, and parts of Utah) are thought to have formed when oceanic crust was subducted at low angles, thereby heating, and melting by devolatilization lithospheric mantle and lower crust hundreds of kilometers east of the subduction zone. This “flat slab” magmatism generally did not extend further east than the longitude of the Colorado Front Range, thus limiting critical minerals covered in this report to Western States (fig. 1; tables 1, 2).
Table 1.
Production of critical minerals in districts and deposits of Western States that are related to subduction magmatism, and possible resources of critical minerals where quantified, semi-quantified, or quantifiable.[Deposits and districts with production of critical minerals as primary products and coproducts are described in Section A; those with byproduct production are described in Section B. Possible significant resources of critical minerals are described in Section C. Assignment of primary products, coproducts, and byproducts in many districts and deposits is uncertain. Mineral systems and deposit types from Hofstra and Kreiner (2020). S-R-V, skarn-replacement-vein; IS, intermediate sulfidation; Cu-Mo-Au, copper-molybdenum-gold; PGE, platinum-group elements; REE, rare earth elements.]
Table 2.
Characteristics of the largest tungsten deposits and resources in Western States.[Latitude and longitude in decimal degrees north and west. S-R-V, skarn-replacement-vein; t, metric ton, Mt, million metric tons; Mst, million short tons; opt, troy ounces per short ton; ft, feet; USGS, U.S. Geological Survey.]
Deposit name | Alternate name | State | Latitude | Longitude | Owner | Production | Resource/ reserve estimate |
---|---|---|---|---|---|---|---|
Andrew Curtis | Andrew Curtis Mine, Andrew Group, Alron #1, Alron #2, Tiffany-Andrew Group, 4 Hi #1, Curtis Claims, Cattle Canyon Placers | Calif. | 34.258 | 117.685 | Curtis Tungsten, Inc. | 7.55 t WO3 concentrate (21–50%) from 1974 to 1982 | Reserves: 6,000 t W measured; 17,000 t W indicated; 216,000 t W inferred (Unruh and Graber, 1982) |
Pilot Mountain | Desert Scheelite, Aurora district | Nev. | 38.379 | 117.871 | Thor Mining PLC | Nominal; “R.C. Armstrong shipped tungsten ore from the Desert Scheelite mine to a custom mill” (Maurer and Wallace, 1956). | 18,600 t W indicated, 8,600 t W inferred (Thor Mining PLC, 2018a, b). |
Centennial | Mount Hamilton mine, Northeast Seligman mine, Treasure Hill mine | Nev. | 39.247 | 115.558 | Mount Hamilton Mining Company | 1997, 7.72 Mst at 0.035 opt Au | Reserve: 18,200 t W from a pre-1978 non-43-101 compliant source and unverified data (SRK Consulting, 2009a). |
Indian Springs | Gambel Ranch or Ludwig Tunnel | Nev. | 41.622 | 114.251 | Utah International, Inc.; Azl Resources Inc.; and Norman Ludwig | Past producer | Resource: 10,900 t W indicated, 9,900 t W inferred (Moran and Stryhas, 2007) |
Browns Lake | Ivanhoe, Lost Creek, Lentung, Red Button mine | Mont. | 45.521 | 112.836 | American Alloy Metals, Inc and Garrand Corp. | From 1953 to 1958, 567,477 short tons at 0.35 percent WO3; 1953–58, 19,200 short tons at 0.18 percent WO3 (Werner and others, 2014) | 14,400 t contained W (Werner and others, 2014) |
Pine Creek | Black Monster, Snow Queen, Union Carbide mine | Calif. | 37.362 | 118.704 | Pine Creek Tungsten Mining Llc, Avocet Ventures Inc., and U.S. Tungsten Corp. as of 1995 | >10,000 short tons; mine closed in 1986 (Werner and others, 2014) | Resource: 10,000 t W (Werner and others, 2014); |
Springer | Stank Hill, Mill City, Nevada Massachusetts | Nev. | 40.782 | 118.133 | Americas Bullion Royalty Corp. | ~10,800 t | 1,400 t W indicated and 6,900 t W inferred (McCandlish and Odell, 2012; SRK Consulting, 2009b) |
Atolia | -- | Calif. | 35.315 | 117.609 | -- | ~828,339 units WO3 (6,568 t W); 94% from veins and 6% from placers; ~54% of total production came from Union mine (developed to depth of 1,021 ft) | “a few thousand tons of 2% ore is in sight in the veins;” mill tailings were being retreated in 1940. Placer deposits contain an estimated 280,000 units WO3 (2,200 t W) and small but unquantified amounts of Au. |
Margerie Glacier | Leo Mark Anthony, Moneta Porcupine mines, Tarr Inlet | Alaska | 59.025 | 137.091 | National Wilderness | None | Resource: 14,500 t W inferred (Brew and others, 1978) |
CuMo | CuMo; CuMo Project | Idaho | 44.034 | 115.783 | American CuMo Mining Corporation; Mosquito Consolidated Gold Mines Ltd as of 2010; Amax Exploration, Inc. as of 1974 also listed in MRDS | None | Resource: 72,000 t W indicated; 42,000 t W inferred (Jones and others, 2011b) |
Sunrise | Brenmac | Wash. | 48.008 | 121.5045 | 1952: W.E. Oldfield; 1976: Ren Mac Mines, Ltd. |
None | 31,730 t W in 64.5 Mt grading 0.319% Cu, 0.071% Mo, 0.062% W, 0.002 opt Au, 0.049-0.088 opt Ag |
Table 2.
Characteristics of the largest tungsten deposits and resources in Western States.[Latitude and longitude in decimal degrees north and west. S-R-V, skarn-replacement-vein; t, metric ton, Mt, million metric tons; Mst, million short tons; opt, troy ounces per short ton; ft, feet; USGS, U.S. Geological Survey.]
Basis of resource/ reserve estimate | Deposit type | Ore minerals present | Elements in deposit | CM in resource | CM domestic consumption threshold (2019) | CM inventory besides W (metric tons) | References |
---|---|---|---|---|---|---|---|
“Extensive mapping, sampling and mill recovery tests” (Unruh and Graber, 1982) | W skarn (S-R-V; scheelite concentrated in shear zones) | Scheelite, barite | W, Ba | W, Ba | >2 years at 27,600 t W | No Ba inventory available | Evans and others (1977); Raney (1982); Unruh and Graber (1982); USGS (2010a); Carroll and others (2018) |
Drillcore, historic and recent | W skarn (S-R-V) | Scheelite, chalcopyrite, azurite | W, Cu, Ag, An, Au | W | >1 year at 13,800 t W | None | Maurer and Wallace (1956); Cowie (1985); Stager and Tingley (1988); Carroll and others (2018); Thor Mining PLC (2018a, b) |
Drill core | W skarn (S-R-V) | Scheelite; chalcopyrite; free gold; sphalerite; galena; pyrite; covellite; bornite; chalcopyrite; bournonite; jamesonite | Cu, Mo, W, Au, Ag, and Sb | W, Sb | >2 years at 27,600 t W but uncertain reliability of resource estimates | No Sb inventory available; Sb classified as a tertiary commodity | USGS (2007); Moran and others (2009); SRK Consulting (2009a, 2012, 2014); Carroll and others (2018) |
Drill core | W skarn (S-R-V) | Scheelite, powellite, molybdenite, tetrahedrite, chalcopyrite, | W, Mo, Cu | W | >1 year at 13,800 t W | None | Slack (1972); Moran and Stryhas (2007); USGS (2010b); Carroll and others (2018) |
Unspecified | W skarn (S-R-V) | Chalcopyrite, powellite, scheelite, bornite, covellite, malachite, pyrrhotite | W, Cu, Mo | W | >1 year at 13,800 t W | None | USGS (1992); Werner and others (2014); Carroll and others (2018) |
Drill core | W skarn (S-R-V) | Scheelite, bornite, chalcocite, chalcopyrite, covellite, molybdenite, powellite | W, Cu, Au, Mo, Ag | W | >1 year at 13,800 t W | None | Newberry (1982); USGS (1996); Kurtak (1998); Werner and others (2014); Carroll and others (2018) |
Drill core | W skarn (S-R-V) | Scheelite, molybdenite, chalcopyrite, sphalerite | W, Mo, Cu | W | <1 year at 13,800 t W | None | Johnson (1977); McCandlish and Odell (2012); Americas Bullion Royalty Corp (2014); Carroll and others (2018) |
Geologic estimation | W vein and W-Au placer | Scheelite | W, Au | W | <1 year at 13,800 t W | None | Lemmon and Dorr (1940); U.S. Bureau of Mines (1943) |
Unspecified | Porphyry Cu | Chalcopyrite, pyrrhotite, powellite, scheelite, molybdenite, arsenopyrite, sphalerite | Cu, W, Mo, Ag, Au | W | >1 year at 13,800 t W | None | Brew and others (1978); USGS (1988); Carroll and others (2018) |
Diamond drilling | Porphyry Cu+Mo | Molybdenite, chalcopyrite, and scheelite, perhaps microscopic gallite (CuGaS2) | Cu, Mo, Ag, W, Re, Ga, Pb, and Zn | W, Re, Ga | >2 years at 27,600 t W | Re has reported concentrations from 0.01 to 0.03 ppm in drill core intervals | USGS (2009); Jones and others (2011a, b); Giroux and others (2015); Carroll and others (2018); Hilscher and Dykes (2018) |
Drill core and underground workings | W-Cu-Mo breccia | Scheelite, chalcopyrite, molybdenite | W, Cu, Mo, Au, Ag | W; Bi, Re in concentrate | >2 years of recent domestic consumption | none | Derkey and others (1990); Lasmanis (1995); USGS (1997) |
Other smaller volume magmatism indirectly linked to plate tectonism includes partial melting of (1) lower crust rocks in the central and eastern Great Basin thickened by contraction and in part heated by oceanic crust during flat-slab subduction, (2) depressurized mantle in slab windows of the southern Cascades magmatic arc that were created by late Cenozoic impingement of the Pacific spreading center on the long-lived convergent subduction zone, and (3) depressurized mantle beneath crust in the Great Basin thinned by extension during the late Cenozoic. The small to moderately sized magmatic-hydrothermal deposits (less than 1 to several million metric tons [Mt]) formed during partial melting of tectonically thickened crust contain small masses of critical minerals. None of the deposits in the mostly small-volume volcanic fields of andesite, dacite, and rhyolite, and lesser basalt that represent magmatism of slab windows and extension younger than 17 mega-annum (Ma) contains appreciable quantities of critical minerals relative to recent domestic consumption.
Known and suspected subduction-related magmatic-hydrothermal deposits that contain critical minerals can be classified under four mineral systems and seven deposit types distinguished largely by characteristics of associated igneous rocks, hydrothermal mineral associations, and proportions of mineral commodities (table 1; Hofstra and Kreiner, 2020). Mineral systems evaluated in this report include porphyry copper-molybdenum-gold (Cu-Mo-Au), alkalic porphyry, porphyry tin (granite related), and reduced intrusion-related. Within these mineral systems deposit types represented include porphyry/skarn copper-gold (Cu-Au), skarn-replacement-vein (S-R-V) tungsten, polymetallic sulfide S-R-V intermediate sulfidation (IS), high-sulfidation gold-silver, low-sulfidation gold-silver, and lithocap alunite (aluminum, potash). Assignment of some deposits containing critical minerals to mineral systems and deposit types is problematic because of incomplete descriptions of deposits, especially small deposits, no known spatial or temporal association of deposits with subduction-related igneous rocks, and (or) deposit characteristics that do not easily fit the classification scheme but contain mineral commodities thought to have been concentrated by subduction-related magmatism. Some deposits containing critical minerals are therefore described in the “Unclassified Magmatic-Hydrothermal Deposits” sections.
Porphyry Cu-Mo-Au mineral systems consist of numerous deposit types including Cu-Mo-Au deposits in intrusions (often porphyritic and mostly calc-alkaline) and polymetallic sulfide S-R-V deposits and lithocap alunite deposits in adjacent and overlying sedimentary and volcanic rocks; some include high- and intermediate-sulfidation deposits (Hofstra and Kreiner, 2020). Porphyry Cu-Mo-Au systems occur within Phanerozoic magmatic arcs adjacent to subduction zones, and supply more than one-half of copper consumed annually worldwide. Critical minerals in porphyry Cu-Mo-Au systems in the Western United States include Al, Sb, As, Bi, Ga, Ge, In, Mn, Ni (designated a critical mineral in 2021), potash (KCl, K2SO4 salts; a critical mineral prior to 2021), Re (a critical mineral prior to 2021), Te, Ti, W, and Zn (designated a critical mineral in 2021) that occur in several deposit types. Critical minerals in other deposit types associated subduction-related magmatism include Al, Sb, Be, Bi, fluorite (CaF2), Li, potash, Ta, Te and Sn in polymetallic sulfide S-R-V-IS deposits, high-sulfidation gold-silver deposits, low-sulfidation gold-silver deposits, lithocap alunite deposits, and in deposits with unclear association with subduction-related magmatism (fig. 2).
Schematic diagram showing spatial relationships of deposit types (black labels) broadly associated with, in part, porphyry copper-molybdenum-gold (Cu-Mo-Au) mineral systems and critical minerals that have been produced or occur in reserves and resources (red labels). PGE, platinum-group elements; REE, rare earth elements.
Alkalic porphyry mineral systems include Cu-Mo-Au deposits and other deposit types that form in alkalic intrusions, in adjacent sedimentary and volcanic rocks, and in veins in intrusions and in adjacent rocks; they also occur within Phanerozoic magmatic arcs and continental rifts. Deposit types of this system in Western States include low-sulfidation gold deposits that are mined for gold and silver and enriched in tellurium, bismuth, and vanadium and fluorspar deposits (table 1).
Porphyry tin (granite-related) mineral systems include deposits that contain the critical minerals beryllium, lithium, niobium, tin, and tantalum. These deposits occur in or near granitic rocks and in pegmatites that reflect partial melting of continental crust to form peraluminous magmas. Deposit types represented in Western States are mostly Precambrian pegmatite deposits that have been mined for beryllium, lithium, niobium, REE, tantalum, and tin (table 1). They are not clearly related to subduction magmatism, contain minor amounts of critical minerals relative to recent domestic consumption, and are not covered in this report.
Reduced intrusion-related mineral systems form in continental magmatic arcs in and adjacent to intrusions that assimilated sedimentary strata containing hydrocarbons and pyrite. Deposit types include gold, skarn copper-molybdenum-tungsten (Cu-Mo-W), polymetallic sulfide S-R-V-IS, disseminated gold-silver, intermediate sulfidation, and graphite. In Western States, few unequivocal reduced intrusion-related deposits are known; several have been mined and explored for gold and lesser silver. Critical mineral concentrations and forms in them are largely unquantified.
The 35 critical minerals initially listed by the Department of the Interior, and the recent additions zinc and nickel, are mineral commodities that are produced and marketed as elements (for example, Al, In, Ni, Te, and Zn), compounds and alloys (for example, GaAs, Si1−xGex, SbPb, InSb, WC, FeV, and FeMn), oxides and carbonates (for example, SbO3, GeO2, Li2CO3, and WO3), and minerals (for example, barite, fluorite, and potash). Critical minerals in Western States that have been produced as primary products, coproducts, and byproducts, and that are known to occur in elevated concentrations in unmined deposits, in interim products of copper concentrators, smelters, and refineries (tailings, slags, slimes, and electrolyte), and in mine dumps, include Al, Sb, As, Be, Bi, fluorite, Ga, Ge, In, Li, Mn, Ni, Nb, Pd, Pt, potash, Re, Ta, Te, Sn, W, V, and Zn.
Descriptions of deposits and resources of the former critical mineral commodities potash and rhenium were completed prior to their delisting and are retained in this report. More recently listed zinc is not covered because of the anticipated time required for evaluation of the large amount of information available. Nickel occurrences in Western States are uncommon, insignificant relative to consumption, and (although in part related to subduction) not related to subduction magmatism. However, nickel in interim products of processing streams of porphyry Cu-Mo-Au ores is potentially recoverable in significant quantities and is correspondingly included where processing information is available.
Elevated concentrations of Al, Sb, As, Bi, Be, Ga, Ge, Mn, potash, and W in some deposits in Western States enabled their production as primary products and coproducts, although most production was small relative to domestic consumption, short lived, and subsidized. Deposits in which critical minerals are primary products are often not distinguishable from coproduct critical minerals because invariably there is insufficient published information to separate them, fluctuating commodity prices can change the relative values of commodities in ore and redefine ore tonnages and grades, and some production was subsidized by guaranteed prices and other federal government policies (for example, War Production Board, 1942; cover image). As used herein, a primary product is a mineral commodity that is essential to the economic viability of a mine (profitability), the basis for exploration, development, and sustained production. A coproduct is one or more mineral commodities produced with other mineral commodities because their combined value is essential for profitable mining. A byproduct is a mineral commodity that is recovered because it adds production value but is not essential to mine profitability.
Production of the primary commodities Cu, Mo, Pb, Zn, Au, and Ag in Western States enabled recovery of most critical minerals, including Sb, As, Bi, Mn, Nb, Pd, Pt, Re, Ta, Te, Sn, W, and V, mostly as byproducts, and in a few deposits as coproducts and primary products. However, many critical minerals in mined deposits occur in low concentrations and small quantities and were never recovered because of unprofitability, and in some cases, no world markets. The porphyry copper-molybdenum (Cu-Mo) deposits in Arizona, New Mexico, Utah, Montana, and Nevada contain small concentrations of critical minerals in ores; however, processing of large tonnages of ore annually for copper and molybdenum recovery concentrates some chalcophile and siderophile critical minerals (Sb, As, Ge, In, Ni, Re, and Te), several of which are episodically recovered and marketed (Re and Te). Unmined porphyry Cu-Mo resources in Alaska, Idaho, and Arizona similarly contain large inventories of these and other chalcophile and lithophile critical minerals (for example, Al, Ti, and Zr) that theoretically could be recovered during ore processing for copper and molybdenum recovery.
In this report, deposits containing critical minerals are grouped by mined deposits in which critical minerals were primary products and coproducts (chap. A) and byproducts (chap. B), by unmined deposits and interim products of copper production with large critical mineral inventories relative to recent domestic consumption (chap. C), and by deposits with elevated concentrations of critical minerals (greater than crustal abundances) in archival specimens and collection samples (chap. D). Within each chapter, deposits, unmined resources, interim products, and specimens and samples are organized by mineral system and deposit type.
With the exception of the Pebble porphyry Cu-Mo and Margerie Glacier tungsten deposits in Alaska, all critical mineral occurrences described in this report are in conterminous Western States. Locations and descriptions of deposits and resources in Alaska that contain critical minerals are available at the USMIN web site (https://mrdata.usgs.gov/deposit/). Deposits and resources containing the critical minerals Be, Li, Nb, PGE, REE, Sn, and Ta as primary products and coproducts, although mostly related to intrusions (for example, Elk Creek niobium, Nebraska; Mountain Pass REE, Calif.; Round Top REE, Tex.; Stillwater Mountains PGE, Mont.; Be-Li-Nb-Sn-Ta pegmatites, N. Mex. and S. Dak.) (USGS and others, 1965, 1975; Bellora and others, 2019; Karl and others, 2021), include deposits in Midwestern States that are not clearly subduction-related and therefore not described below.
This report (1) provides a historical perspective of critical minerals produced from subduction-related magmatic-hydrothermal systems in the Western United States, (2) describes significant inventories of critical minerals in unmined deposits and mine reserves, and (3) tracks critical minerals in interim products of copper refineries where they comprise significant inventories but mostly are not recovered. The report is intended to inform policy makers of the approximate masses of domestic critical minerals that conceivably could become supplies for consumption if economic incentives for their mining and recovery are enabled.
Brief History of Critical Minerals
The concept of critical minerals arose in the early 20th century with the expanded application of alloys and compounds of C, Cr, Fe, Mn, Ni, and W that greatly improved metal durability, machining efficacy, and armament effectiveness (Lovering, 1944; Andrews, 1955; Limbaugh, 2006, 2010; Schmidt, 2012). These ferroalloys and compounds became essential to national defense and industrial competitiveness. Their components, variously termed critical or strategic minerals, faced supply uncertainty because domestic production since World War I has been insufficient for consumption. Concerns over importation security of tungsten and other commodities crucial for machining and armaments escalated in the 1930s and during World War II. Price guarantees (for example, Sb, As, Mn, and W) (War Production Board, 1942; cover image) and other forms of subsidization by the federal government increased domestic production prior to and during World War II and the Korean War; they were episodically extended into the 1960s through much of the Cold War era. However, peak tungsten production, for example, from domestic mines never exceeded 50 percent of required World War II supplies (approximately equivalent to consumption) (fig. 3; Morgan, 1983); then, as now, importation with trade route protection, as required, secured necessary imports.
Bar chart of domestic tungsten supplies during World War II and pre- and post-war years derived from U.S. mines and imports (Morgan, 1983).
Domestic critical mineral deposits, reserves, resources, and inventories described in this report attest to small low-grade deposits and resources of tungsten and other critical minerals, non-recovery of critical minerals at operating and shuttered or demolished refineries, and disincentives to explore for and produce critical minerals in the United States. Many of the largest and highest-grade domestic metal deposits were discovered and mined in the 19th and 20th centuries when there were no or small world markets for commodities subsequently deemed critical or strategic minerals. Comprehensive descriptions of these major deposits and districts (for example, Ridge, 1968) seldom include critical mineral commodities because they had no bearing on production economics and there was no to small demand for many. Imported supplies were generally deemed secure until the vulnerability of oceanic shipping was revealed by World Wars I and II.
Before, during, and after World War II and during the Cold War era, numerous investigations of domestic sources of critical mineral commodities were conducted by the U.S. Bureau of Mines (USBM) and USGS to address wartime shortages and importation vulnerability (USBM, 1941a; Moon, 1950; Foster, 1988). Several “underground stockpiles” of unmined, marginal “ore” were blocked out (measured, indicated, and inferred reserves) by drill holes, surface excavations, underground development, and metallurgical test work. These marginal ores were assumed recoverable, if needed, whereas price guarantees were used to encourage domestic critical mineral production by the mining industry. Some cumulative tonnages of marginal ores defined by USBM investigations are likely too small or scattered or have grades that are too low to mine profitably today without subsidization; for example, 1.380 million short tons (Mst) (1.25 Mt) grading 33 to 53.5 percent fluorite are distributed among 36 deposits, approximately 18 Mst (16.4 Mt) grading 9 to 23.2 percent manganese are distributed among 39 deposits, and 10.6 Mst (9.6 Mt) of alunite in two deposits grading 21 to 31 percent Al2O3 (table 1 in Moon, 1950).
Occurrences of many critical minerals associated with subduction-related igneous rocks in Western States are variably described in War Mineral Reports (USBM, 1942–1945), in collaborative reports by the USGS and state geological surveys (for example, USGS and Montana Bureau of Mines and Geology, 1963; USGS and Nevada Bureau of Mines, 1964; USGS and others, 1964, 1965, 1966a, 1969, 1975), and in topical publications by the USGS, most of which stem from World War II and Cold War era supply concerns.
Limitations and Assumptions
Evaluation of critical minerals in this report was conditioned by the quality of published concentrations and brevity of deposit descriptions, by incomplete access to unpublished drill hole records and reserves of mined and unmined deposits, and by general disinterest in critical mineral exploration and recovery. These limitations lead to uncertainty in classification of some deposits and necessitated application of a mass threshold to distinguish significant domestic inventories of critical minerals based on their current consumption.
Quantification of critical minerals is limited by accuracy of published concentrations, especially low concentrations reported in pre-2000 publications. Recovery (free market and subsidized) of some chalcophile, siderophile, and lithophile critical mineral commodities was usually enabled by average grades and grade ranges of percents to tens of percents (for example, Sb, fluorite, Mn, and W). Production at these grades obtained from published sources is therefore considered reasonably accurate. However, multi-element analyses of critical minerals and other commodities in ores and rocks used in mineral deposit investigations before approximately 2000 had insufficient precision and detection limits to accurately quantify chalcophile and siderophile critical minerals that mostly occur in low concentrations (less than 1 percent; for example, Bi, PGE, and Te) in deposits described in this report. Over the past two decades multi-element analyses with lower detection limits have been increasingly used in mineral deposit exploration programs and reserve delineation of unmined deposits. Concentrations of critical minerals in exploration and deposit delineation drill holes that represent large masses of mineralized rocks are used in this report, as available, to evaluate critical mineral resources and inventories in unmined deposits and resources, in addition to those inventories determined from production and refining records (tables 3–15). Multi-element analyses of archival specimens and collection samples of mineralized rocks also reveal elevated concentrations of critical minerals that portend possibly significant inventories in numerous mining districts in Western States (tables 16–19). Known and suspected sites of critical minerals in deposits, resources, and interim recovery products are listed in table 20 and described in the text.
Table 3.
Element concentrations averaged from multi-element geochemical analyses of drill hole intervals in the Sunnyside porphyry copper-(molybdenum-silver) system, Santa Cruz County, Arizona.[Data from Granitto and others (2021). ppb, parts per billion; ppm, parts per million; wt %, weight percent; n/a, not available; DDH, diamond drill hole.]
Table 3.
Element concentrations averaged from multi-element geochemical analyses of drill hole intervals in the Sunnyside porphyry copper-(molybdenum-silver) system, Santa Cruz County, Arizona.[Data from Granitto and others (2021). ppb, parts per billion; ppm, parts per million; wt %, weight percent; n/a, not available; DDH, diamond drill hole.]
Table 4.
Multi-element analyses of drill hole and surface samples for preparation of standards and bulk metallurgical test samples, Hardshell-Alta-Hermosa silver-manganese-lead-zinc replacement deposit, Santa Cruz County, Arizona.[Data from Granitto and others (2021). Determined by WEII-21 (weight of submitted sample), ME-GRA21 (multi-element-gold by fire assay and gravimetric finish), ME-MS61 (multi-element-mass spectrometry 61 elements), Hg-CV41 (mercury-cold vapor), Ag-OG62 (silver by hydrofluoric-nitric-perchloric acid digestion with hydrochloric acid leach, inductively coupled plasma-atomic emission spectrography or atomic absorption spectrography finish), ), Pb-OG62 (lead by hydrofluoric-nitric-perchloric acid digestion with hydrochloric acid leach, inductively coupled plasma-atomic emission spectrography or atomic absorption spectrography finish), and Zn-OG62 (zinc by hydrofluoric-nitric-perchloric acid digestion with hydrochloric acid leach, inductively coupled plasma-atomic emission spectrography or atomic absorption spectrography finish). ppm, parts per million; wt %, weight percent.]
Table 5.
Concentrations of primary commodities and critical minerals in approximately 7,520 intervals of diamond drill holes in the Pebble porphyry copper deposit, Alaska.[Data from Granitto and others (2021). ppm, parts per million.]
Table 6.
Average concentrations of primary commodities and critical minerals in approximately 10,930 intervals of ~66 diamond drill holes and rotary drill holes in the CuMo porphyry copper-molybdenum deposit; sorted for copper concentrations of 1,000 ppm or more.[Data from Granitto and others (2021). Concentrations determined by AES-HF (atomic emission spectroscopy-hydrofluoric acid digestion), MS-HF (mass spectrometry-hydrofluoric acid digestion), and CM-HF (colorimetric spectrophotometry-hydrofluoric acid digestion. Silver, copper, molybdenum, and tungsten concentrations were determined in 835 intervals by AA-F-AE-P (atomic absorption-fluoride-atomic emission-phosphorus) and CM-HF. ppm, parts per million; wt %, weight percent.]
Table 7.
Average concentrations of antimony, arsenic, bismuth, and tungsten in drill hole intervals in and below gold-silver-antimony resources in the Yellow Pine district, Valley County, Idaho, composited for metallurgical recovery testing.[Data from Midas Gold, Inc. Concentrations determined by ICPMS (inductively coupled plasma mass spectrometry). g/t, grams per metric ton; Mt, million metric tons; DDH, diamond drill holes]
As of December 2020 (NS Energy, 2021).
Table 8.
Rotary, hammer, reverse-circulation, core, blast, drill holes and bulk, grab and cut surface and underground samples (some from historic collections) in the Cripple Creek gold district, Teller County, Colorado.[Data from Granitto and others (2021). ppb, parts per billion; opt, troy ounces per short ton; ppm, parts per million; wt %, weight percent; MS61, mass spectrometry-61 elements; BLD, below limit of detection.]
Table 9.
Compositions of anode copper from domestic copper smelters, 1986–2018.[Concentrations of copper and minor elements in copper at several stages of refining (matte, blister, anode) and in electrolytic cell residue (slime, anode mud) and electrolyte, are determined for quantification of precious metals and control of deleterious and beneficial elements. wt %, weight percent; ppm, parts per million; ?, queried as in original source.]
Smelter | Year | Anode copper composition | Source | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cu (wt %) | Ag | Au | S | Se | Te | As | Sb | Bi | Pb | Fe | Ni | Sn | O | |||
(ppm) | ||||||||||||||||
ASARCO Inc. | 2018 | 99.51 | 445 | 1.4 | 20 | 509 | 61 | 376 | 82 | 177 | 158 | 657 | 148 | -- | 1,727 | M. Moats, personal commun., 2019 |
Anodes from smelters at El Paso, Tex., and Hayden, Ariz., some from other smelters, and scrap | 2005 | 99.43 | 934 | 2.8 | 16 | 640 | 120 | 380 | 260 | 80 | 80 | 40 | 230 | -- | 1,800 | Moats and others (2007) |
2003 | 99.26 | 1,545 | 5.3 | 18 | 790 | 120 | 490 | 410 | 210 | 140 | 40 | 450 | -- | 1,800 | Moats and others (2013), Robinson and others (2003) | |
1999 | -- | -- | -- | -- | -- | -- | 390 | 340 | 130 | 110 | -- | -- | -- | -- | Larouche (2001) | |
1998 | 99.12 | 2,252 | 19.5 | 22 | 600 | 100 | 770 | 510 | 200 | 320 | 40 | 990 | -- | 1,600 | Davenport and others (1999) | |
1994 | 99.2 | 1,500 | 10 | 14 | 850 | 90 | 460 | 430 | 100 | 280 | 90 | 910 | -- | 1,800 | Schloen and Davenport (1995) | |
1991 | 99.3 | 1,200 | -- | -- | 600 | 100 | 400 | 550 | 45 | 500 | -- | 1,700 | -- | 1,600 | Schloen (1991) | |
1987 | 99.3 | 1,200 | -- | -- | 600 | 100 | 400 | 550 | 45 | 500 | -- | 1,700 | -- | 1,600 | Schloen (1987) | |
1986? | 98.6–99.4 | -- | -- | 10–30 | 600–700 | 40–200 | 300–900 | 500–800 | 20–60 | 300–400 | -- | 400–800 | 10–50 | 1,500 | Ramachandran and Wildman (1987) | |
Phelps Dodge/ Freeport-McMoRan, El Paso, Tex. | 2018 | 98.9–99.7 | 160–1,200 | 1–15 | 7–30 | 200–1,000 | 10–100 | 70–700 | 50–300 | 20–200 | 10–600 | 5–100 | 50–600 | -- | 1,050–2,400 | M. Moats, personal commun. 2019 |
Anodes from smelters at several sites including Miami and Douglas, Ariz. | 2005 | 98.9–99.7 | 160–1,200 | 1–15 | 7–30 | 200–1,000 | 10–100 | 100–3,000 | 30–500 | 5–100 | 10–600 | 5–100 | 50–600 | -- | 1,050–2,400 | Moats and others (2007) |
2003 | 99.5–99.7 | 160–412 | 5.15–7.2 | 7–30 | 200–400 | 40–85 | 10–900 | <1–60 | 20–130 | 50–100 | <1–80 | 50–700 | -- | 1,050–2,400 | Moats and others (2013), Robinson and others (2003) | |
1998 | 99.5–99.7 | 160–412 | 5.15–7.20 | 7–30 | 200–400 | 40–85 | 10–900 | <1–60 | 20–130 | 10–50 | <1–80 | 50–350 | -- | 1,050–2,400 | Davenport and others (1999) | |
1994 | 99.5–99.7 | 60–700 | 1.7–17 | 7–60 | 133–300 | 20–190 | 10–900 | 10–260 | 20–100 | 20–400 | 2–60 | 100–200 | -- | 1,200–1,600 | Schloen and Davenport (1995) | |
1991 | 99.6 | 200–300 | -- | -- | 125–400 | 20–100 | 50–300 | 30–200 | 10–100 | 20–200 | -- | 90–800 | -- | 1,200–1,700 | Schloen (1991) | |
1987 | 99.5 | 225–300 | -- | -- | 200–450 | 25–50 | 25–50 | 35–50 | 5–15 | 15–150 | -- | 100–700 | -- | 1,400–2,800 | Schloen (1987) | |
Kennecott/ Rio Tinto Utah Copper | 2014 | 99 | 430 | 34 | 27 | 614 | 81 | 1,966 | 30 | 529 | 2,531 | 28 | 316 | -- | 1,555 | Moats and others (2014b) |
Anodes from smelters at Garfield, Utah, and Magna, Utah (co-sited with copper refinery) | 2003 | 99 | 462 | 52 | 38 | 784 | 118 | 1,113 | 46 | 679 | 2,121 | 13 | 271 | -- | 1,709 | Moats and others (2007), Robinson and others (2007) |
2003 | 99 | 462 | 52 | 38 | 784 | 118 | 1,113 | 46 | 679 | 2,121 | 13 | 271 | -- | 1,709 | Moats and others (2013), Robinson and others (2003) | |
1999 | -- | -- | -- | -- | -- | -- | 1,000–4,000 | 100–125 | 400–600 | 2,500–4,000 | -- | 215 | -- | -- | Larouche (2001), Davenport and others (2001) | |
1998 | 99.1 | 500 | 50 | 20 | 600 | 150 | 2,000 | 150 | 500 | 3,000 | 10 | 250 | -- | 2,200 | Davenport and others (1999) | |
1994 | 99.4 | 500 | 60 | 30 | 500 | 60 | 1,000 | 100 | 300 | 2,500 | 20 | 300 | -- | 2,100 | Schloen and Davenport (1995) | |
1991 | 99.6 | 538 | -- | -- | 500 | 150 | 820 | 80 | 80 | 140 | -- | 210 | -- | 1,930 | Schloen (1991) | |
1987 | 99.6 | 403 | -- | -- | 500 | 140 | 560 | 60 | 33 | 63? | -- | 220 | -- | 900–1,200 | Schloen (1987) | |
Cyprus/ Phelps Dodge, Miami, Ariz. | 2003 | 99.5 | 500 | 2.5 | 18 | 320 | 12 | 680 | 100 | 12 | 90 | 12 | 600 | -- | 1,350 | Robinson and others (2003) |
1999 | -- | -- | -- | -- | -- | -- | 770 | 132 | 13 | 129 | -- | 514 | -- | Larouche (2001) | ||
1998 | 99.5 | 510 | 94 | 10 | 303 | 25 | 90 | 270 | 20 | 127 | 12 | 377 | -- | 1,500 | Davenport and others (1999) | |
1994 | 95.5 | 510 | 24 | 10 | 303 | 25 | 90 | 270 | 20 | 127 | 12 | 377 | -- | 1,500 | Schloen and Davenport (1995) | |
1991 | 99.5 | 400 | -- | -- | 300 | 20 | 80 | 150 | 12 | 100 | -- | 600 | -- | 1,600 | Schloen (1991) | |
White Pine Copper Refinery/ Copper Range Co./ BHP, White Pine, Mich. | 2003 | 99.55 | 550 | 25 | 15–45 | 400–600 | 50–100 | 350–400 | 20–30 | 10–20 | 150–450 | 50–150 | 50–150 | -- | 1,200–1,800 | Moats and others (2007) |
2003 | 99.55 | 550 | 25 | 15–45 | 400–600 | 50–100 | 350–400 | 20–30 | 10–20 | 150–450 | 50–150 | 50–150 | -- | 1,200–1,800 | Robinson and others (2003) | |
1998 | 99.5 | -- | -- | 40 | 350 | 100 | 300 | 30 | 20 | 150 | 50 | 50 | -- | 1,600 | Davenport and others (1999) | |
1994 | 99.6 | 700 | 3.5 | 6 | 250 | 30 | 250 | 25 | 50 | 15 | 35 | 110 | -- | 1,500 | Schloen and Davenport (1995) | |
1991 | 99.5–99.8 | 700 | -- | -- | 25–100 | 10–60 | 150 | 25 | 5 | 30 | -- | 40 | -- | 1,500–2,000 | Schloen (1991) | |
1987 | 99.5–99.8 | 700 | -- | -- | 25 | -- | 200 | 50 | 5 | 80 | -- | 150 | -- | 1,000–1,500 | Schloen (1987) | |
Magma Metals Co./ BHP, San Manuel, Ariz. | 1998 | 99.7 | 302 | 21.3 | 18 | 410 | 29 | 616 | 39 | 59 | 31 | 14 | 87 | -- | 1,306 | Davenport and others (1999) |
1994 | 99.7 | 375 | 8 | 20 | 450 | 40 | 320 | 70 | 70 | 50 | 15 | 120 | -- | 1,400 | Schloen and Davenport (1995) | |
1991 | 99.8 | 217 | -- | -- | 439 | 12 | 196 | 68 | 19 | 35 | -- | 68 | -- | 1,483 | Schloen (1991) | |
1987 | 99.78 | 175 | -- | -- | 415 | 6 | 24 | 73 | 3 | 63 | -- | 121 | -- | 900–1,200 | Schloen (1987) |
Table 10.
Compositions of tank house slimes from domestic copper refineries, 1986-2018.[Concentrations of copper and minor elements in copper at several stages of refining (matte, blister, anode) and in electrolytic cell residue (slime, anode mud) and electrolyte, are determined for quantification of precious metals and control of deleterious and beneficial elements. kg, kilogram; t, metric ton; wt %, weight percent; NR, not recorded.]
Refinery | kg slimes/ t anode | Slimes composition (wt %) | Source | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cu | Ag | Au | Pt | Pd | S | Se | Te | As | Sb | Bi | Pb | Fe | Ni | |||
ASARCO Inc., Amarillo and El Paso, Tex., Hayden, Ariz.; Amarillo, Tex. | 2.01 | 2.2 | 16.8 | 0.07 | -- | -- | -- | 23.2 | 0.8 | 3.4 | 2.0 | 6.8 | 7.6 | -- | -- | M. Moats, personal commun., 2019 |
Notes: refined anodes from ASARCO smelters at El Paso, Tex., and Hayden, Ariz.; also refines blister from other smelters, and #2 scrap | 2.2 | 19.6 | 18.6 | 0.12 | -- | -- | -- | 14.1 | 1.45 | 2.91 | 2.86 | 0.44 | 0.15 | -- | 0.74 | Moats and others (2007) |
4.3 | 4.63 | 48.12 | 0.18 | -- | -- | -- | 28.13 | 2.25 | 2.73 | 4.05 | 0.87 | 0.53 | -- | -- | Moats and others (2013), Robinson and others (2003) | |
7.42 | 3.7 | 38.4 | 0.29 | -- | -- | -- | 16.5 | 1 | 2.1 | 4.4 | 0.8 | 9.1 | -- | 1.7 | Davenport and others (1999) | |
6 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen and Davenport (1995) | ||||||||||||||
5 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1991) | ||||||||||||||
5 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1987) | ||||||||||||||
NR | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Ramachandran and Wildman (1987) | ||||||||||||||
Phelps Dodge/ Freeport-McMoRan, El Paso, Tex. | 0.9–1.8 | 1 | 18 | 0.2 | -- | -- | 12 | 19 | 0.4 | 3 | 5 | 0.7 | 5 | 0 | 0.1 | M. Moats, personal commun., 2019 |
27.1 | 12.2 | 0.12 | 0.0007 | 0.006 | -- | 8.8 | 3.1 | 1.7 | 0.66 | -- | 4.65 | 0.08 | 0.64 | Hait and others (2009) | ||
4–6 | 1 | 22 | 0.2 | -- | -- | 12 | 20 | 0.4 | 2 | 4 | 0.7 | 5 | 0.04 | 0.05 | Moats and others (2007) | |
4.4–6.4 | 25 | 17 | 0.2 | -- | -- | 12 | 10 | 2 | 2 | 1.7 | 1.7 | 3 | <1 | <1 | Moats and others (2013), Robinson and others (2003) | |
2.2–4.4 | 25 | 17 | 0.2 | -- | -- | 12 | 12 | 2 | 2 | 1.7 | 1.7 | 3 | <1 | <1 | Davenport and others (1999) | |
2.2–4.4 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen and Davenport (1995) | ||||||||||||||
1.5 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1991) | ||||||||||||||
1.75 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1987) | ||||||||||||||
Kennecott/ Rio Tinto Utah Copper, Magna, Utah | 10 | 25 | 4.5 | 0.4 | -- | -- | -- | 7.5 | 1 | 5 | 0.25 | 5 | 25 | 0.25 | 0.05 | M. Moats, personal commun., 2019 |
9.7 | 30 | 5 | 0.5 | -- | -- | 0 | 5 | 1 | 5 | 1 | 3 | 30 | 0.25 | 0.05 | Moats and others (2007), Robinson and others (2007) | |
9.7 | 30 | 5 | 0.5 | -- | -- | 0 | 5 | 1 | 5 | 1 | 3 | 30 | 0.25 | 0.05 | Moats and others (2013), Robinson and others (2003) | |
9.7 | 20 | 5 | 0.5 | -- | -- | 0 | 5 | 1 | 5 | 1 | 3 | 30 | 0.25 | 0.05 | Davenport and others (1999) | |
9.7 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen and Davenport (1995) | ||||||||||||||
5.3 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1991) | ||||||||||||||
5.3 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1987) | ||||||||||||||
Cyprus/ Phelps Dodge, Miami, Ariz. | 2 | 0.5 | 17 | 0.1 | -- | -- | 6 | 18 | 0.3 | 0.7 | 2 | 0.3 | 2 | 0.1 | 0.02 | Robinson and others (2003) |
1.6 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Davenport and others (1999) | ||||||||||||||
9.7 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen and Davenport (1995) | ||||||||||||||
1 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1991) | ||||||||||||||
White Pine Copper Refinery/ Copper Range Co./ BHP, White Pine, Mich. | 2.7 | 1–3 | 20 | 0.9 | -- | -- | 7 | 25 | 2 | 1 | 0.5 | 0.75 | 15 | 0.2 | 0.1 | Moats and others (2007) |
2.7 | 1–3 | 20 | 0.9 | -- | -- | 7 | 25 | 2 | 1 | 0.5 | 0.75 | 15 | 0.2 | 0.1 | Robinson and others (2003) | |
4 | 30 | 14.5 | 1.1 | -- | -- | -- | 16 | 2 | 1.2 | 0.5 | 0.5 | 7 | 0.05 | 0.05–0.1 | Davenport and others (1999) | |
1 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen and Davenport (1995) | ||||||||||||||
2 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1991) | ||||||||||||||
2 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1987) | ||||||||||||||
Magma Metals Co./ BHP, San Manuel, Ariz. | 1.6 | 1.0 | 16.0 | 1.2 | -- | -- | 26.0 | 1.1 | 0.2 | 0.2 | 0.8 | 0.8 | 2.1 | 0.2 | 0.004 | Davenport and others (1999) |
3.5 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen and Davenport (1995) | ||||||||||||||
NR | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1991) | ||||||||||||||
1.01 | NO SLIME ANALYSES REPORTED; COULD BE CALCULATED FROM REPORTED CATHODE ANALYSES | Schloen (1987) |
Table 11.
Copper and minor element concentrations in matte and blister copper and tank house slimes of domestic copper refineries, 1897–1973.[Concentrations of copper and minor elements in copper at several stages of refining (matte, blister, anode) and in electrolytic cell residue (slime, anode mud) and electrolyte, are determined for quantification of precious metals and control of deleterious and beneficial elements. wt %, weight percent; ppm, parts per million; opt, troy ounces per short ton.]
Blister Cu (~98%) is produced from matte by air oxidation of Cu and Fe sulfide minerals and separation from Fe oxide slag; it has characteristic nodular surfaces from quenched SO2 bubbles.
Table 11.
Copper and minor element concentrations in matte and blister copper and tank house slimes of domestic copper refineries, 1897–1973.[Concentrations of copper and minor elements in copper at several stages of refining (matte, blister, anode) and in electrolytic cell residue (slime, anode mud) and electrolyte, are determined for quantification of precious metals and control of deleterious and beneficial elements. wt %, weight percent; ppm, parts per million; opt, troy ounces per short ton.]
Pt (opt) |
Pd (opt) |
Te (wt %) |
Te (ppm) |
Se (wt %) |
Se (ppm) |
Se+Te (ppm) |
Bi (wt %) |
Bi (ppm) |
As (wt %) |
As (ppm) |
Sb (wt %) |
Sb (ppm) |
Source |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
-- | -- | -- | 50- 270- 190 |
-- | -- | -- | -- | 50- 550- 240 |
-- | 340- 1,080- 740 |
-- | 480- 1,570- 990 |
Keller, 1897 |
-- | -- | -- | -- | -- | -- | 150–500 | -- | -- | -- | 140–500 | -- | 100–330 | Douglas, 1899 |
-- | -- | 0.0088 | 88 | 0.0113 | -- | -- | 0.0044 | 44 | -- | -- | -- | -- | Sharwood, 1911 |
-- | -- | 0.001–0.01 | 10–100 | 0.001–0.01 | -- | -- | 0.03–0.05 | 300–500 | -- | -- | -- | -- | |
-- | -- | 2–3 | 20,000–30,000 | 2–3 | -- | -- | 2–3 | 20,000–30,000 | -- | -- | -- | -- | |
0.0034 | 0.0118 | 0.0028 | 2.8 | 0.028 | -- | -- | 0.0031 | 31 | -- | -- | -- | -- | Eiler, 1913 |
0.0102 | 0.044 | 0 | 0 | 0.0551 | -- | -- | 0.0002 | 2 | -- | -- | -- | -- | |
0.0133 | 0.0649 | 0.0336 | 33.6 | 0.0133 | -- | -- | 0.0094 | 94 | -- | -- | -- | -- | |
0.0132 | 0.0061 | 0.0017 | 1.7 | 0.018 | -- | -- | 0.0137 | 137 | -- | -- | -- | -- | |
0.0071 | 0.0333 | 0 | 0 | 0.021 | -- | -- | 0.0029 | 29 | -- | -- | -- | -- | |
-- | -- | -- | 170 | -- | 90 | -- | -- | 38 | -- | 1,180 | -- | 530 | Lapee, 1962 |
-- | -- | -- | 1,030 | -- | 110 | -- | -- | 25 | -- | 810 | -- | 420 | |
-- | -- | -- | 840 | -- | 120 | -- | -- | 57 | -- | 880 | -- | 730 | |
-- | -- | -- | 230 | -- | 200 | -- | -- | 33 | -- | 640 | -- | 220 | |
-- | -- | 5.14 | -- | 5.31 | -- | -- | -- | -- | -- | 56,300 | -- | 46,600 | Mosher, 1934 |
-- | -- | 3.49 | -- | 4.51 | -- | -- | -- | -- | -- | 36,000 | -- | 139,700 | |
-- | -- | 0.045 | -- | 0.061 | -- | -- | 0.008 | -- | 0.064 | -- | 0.031 | -- | Schloen and Elkin, 1954 |
-- | -- | 0.02 | -- | 0.07 | -- | -- | 0.002 | -- | 0.06 | -- | 0.1 | -- | |
-- | -- | -- | -- | 0.051 | -- | -- | 0.007 | -- | 0.06 | -- | 0.198 | -- | |
-- | -- | 0.024 | -- | 0.012 | -- | -- | 0.003 | -- | 0.059 | -- | 0.027 | -- | |
0.2 | 2.3 | 3 | -- | 12 | -- | -- | -- | -- | 2 | -- | 0.5 | -- | Leigh, 1973 |
Table 12.
Critical mineral concentrations in porphyry copper-(molybdenum) deposits based on average concentrations in drill hole intervals, deposit domains, mineralogical investigations, and resource and reserve tonnages.[Cu-(Mo), copper-(molybdenum); Mt, million metric tons; wt %, weight percent; ppm, parts per million; gd, granodiorite; cpy, chalcopyrite; bn, bornite; cc, chalcocite; en, enargite; tn, tennantite; NR, not reported; est., estimated; USGS, U.S. Geological Survey.]
Table 12.
Critical mineral concentrations in porphyry copper-(molybdenum) deposits based on average concentrations in drill hole intervals, deposit domains, mineralogical investigations, and resource and reserve tonnages.[Cu-(Mo), copper-(molybdenum); Mt, million metric tons; wt %, weight percent; ppm, parts per million; gd, granodiorite; cpy, chalcopyrite; bn, bornite; cc, chalcocite; en, enargite; tn, tennantite; NR, not reported; est., estimated; USGS, U.S. Geological Survey.]
Concentrations of critical minerals (value used for inventory in table 13)1 | Data source; references | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Sb | As | Bi | Ge | In | PGE | Re | Sn | Te | W | |
(ppm) | ||||||||||
4 | 41 | 1 | <1 | <1 | <0.02 | <1 | 2 | <1 | 13 | Table 5; USGS (2013a) |
1 | 6 | 3 | <1 | <1 | NR | <1 | 7 | <1 | 61 | Table 6; SRK Consulting (2020) |
12 | 27 | <10 | NR | NR | NR | NR | 2 | 34 | 9 | Table 7; Vikre and others (2014), Chaffee (2019) |
-- | -- | -- | -- | -- | -- | -- | -- | -- | -- | |
14–105 (60) | 17–183 (100) | 2–11 (6) | 1–2 (1.5) | <1 | <0.002 | 36 | 4–8 (6) | <1 | 14–65 (40) | Table 3; Vikre and others (2014) |
22–88 (55) | 230–611 (420) | 5–66 (35) | 2–4 (3) | 1–3 (2) | 0.001 | NR | 9–16 (13) | NR | 46–55 (50) | -- |
7.7 | 22.5 | 438.8 | 2.8 | 3.6 | NR | 31.6 | 4.1 | 16.5 | 31 | -- |
1,082 | 914 | 1 | 0.2 | 0.1 | NR | 0 | 2 | 4 | 10 | Table 4; South32 Limited (2020) |
-- | -- | -- | -- | -- | -- | -- | -- | -- | -- | South32 Limited (2020) |
21 | 210 | 111 | 4 | 2 | <0.012 | NR | 12 | NR | 123 | Table 3; Vikre and others (2014) |
-- | -- | <5.4 | -- | 0.07 | 0.014 | 0.04–0.27 | 6.9 | 0.34–4.8 | -- | Table 4 |
-- | -- | -- | -- | -- | -- | -- | -- | -- | -- | -- |
-- | -- | -- | -- | -- | -- | -- | -- | -- | -- | -- |
1.8 | 8.7 | 5.4 | <1 | <1 | NR | 0.55 | 6.9 | 4.8 | 21 | Austin and Ballantyne (2010) |
3.7 | 10.7 | 0.9 | <1 | <1 | NR | 0.09 | 1.3 | <1 | 12 | -- |
6.6 | 8.8 | 0.7 | <1 | NR | NR | NR | 0.5 | <1 | 1 | -- |
20.4 | 1,579 | -- | -- | -- | -- | -- | -- | -- | -- | Gunter and Austin (1997) |
<1 | 5.2 | <1 | -- | <1 | -- | <1 | 1.5 | <1 | 2.9 | Cohen (2011), Hudbay Minerals, Inc. (2021); J. Dilles, Oregon State University, written commun., 2021 |
-- | -- | -- | -- | -- | -- | -- | -- | 2.4 | -- | Table 12; Lori (2010) |
Table 13.
Critical mineral inventories in porphyry copper-(molybdenum) deposits based on average concentrations in drill hole intervals, deposit domains, mineralogical investigations, and resource/reserve tonnages.[Cu-(Mo), copper-(molybdenum); Mt, million metric tons; t, metric tons; est., estimated; USGS, U.S. Geological Survey.]
Porphyry Cu-(Mo) system | Resource (Mt) |
Reserve (Mt) |
Critical mineral inventories | Data source; references | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Sb | As | Bi | Ge | In | PGE | Re | Sn | Te | W | |||||
(t) | ||||||||||||||
Pebble, Alaska | 7,510 | -- | 30,040 | 307,910 | 7,510 | -- | -- | -- | -- | 15,020 | -- | 97,630 | Table 5; USGS (2013a) | |
CuMo, Idaho (>0.1 wt % Cu) | ~2,270 | -- | 2,270 | 13,620 | 6,810 | -- | -- | -- | -- | 15,898 | -- | 138,470 | Table 6; SRK Consulting (2020) | |
Red Mountain, Ariz. | 385 | -- | 4,620 | 10,395 | -- | -- | -- | -- | -- | -- | 13,090 | 3,465 | Table 7; Vikre and others (2014); Chaffee (2019) | |
100–150 | -- | -- | -- | -- | -- | -- | -- | -- | -- | -- | -- | |||
Sunnyside, Ariz. | 1,500 | -- | 90,000 | 150,000 | 9,000 | 2,350 | -- | -- | 54,000 | 9,000 | -- | 60,000 | Table 3; Vikre and others (2014) | |
800 | -- | 44,000 | 336,000 | 28,000 | 2,400 | 1,600 | -- | -- | 10,400 | -- | 24,800 | |||
1Est. 20 | -- | 154 | 450 | 8,776 | 56 | 72 | -- | 632 | 82 | 330 | 620 | |||
Hardshell-Alta-Hermosa, Ariz. | 2Est. 33 | -- | 35,706 | 3,016 | 33 | -- | -- | -- | -- | 66 | 132 | 330 | Table 4; South32 Limited, 2020 | |
Ventura, Ariz. | 3.6 | -- | 75.6 | 756 | 399.6 | 14.4 | 7.2 | -- | -- | 43.2 | -- | 442.8 | Table 3; Vikre and others (2014) | |
Bingham, Utah | -- | 552 | -- | -- | 4,200 | -- | 60 | 12 | 36–228 | 5,800 | 285–4,000 | -- | Table 4 | |
285 | -- | -- | -- | -- | -- | -- | -- | -- | -- | -- | -- | |||
20 | -- | -- | -- | -- | -- | -- | 3.8–20 | -- | -- | -- | -- | |||
285 | 552 | 513; 994 | 2,470; 4,802 | 1,539; 2,981 | -- | -- | -- | 157; 304 | 1,682; 3,809 | 1,368; 2,650 | 5,985; 11,592 | Gunter and Austin (1997); Austin and Ballantyne (2010); Rio Tinto (2021b) | ||
-- | -- | 1,055; 2,042 | 3,050; 5,906 | 257; 497 | -- | -- | -- | -- | 371; 718 | -- | 3,420; 6,624 | |||
-- | -- | 1,881; 3,643 | 2,508; 4,858 | 200; 386 | -- | -- | -- | -- | 143; 276 | -- | 29; 55 | |||
Yerington, Nev. | 2,219 | -- | -- | 11,539 | -- | -- | -- | -- | -- | 3,329 | -- | 6.435 | Cohen (2011); Hudbay Minerals, Inc. (2021); J. Dilles, Oregon State University, written commun., 2021 | |
159 | -- | -- | -- | -- | -- | -- | -- | -- | -- | -- | -- | Table 8; Lori (2010); Independent Mining Consultants, Inc. (2022) |
Critical mineral resources calculated using concentrations in diamond drill hole intercepts and an estimated tonnage.
Critical mineral resources calculated from separate concentrations in metallurgical composites and resource tonnage (South32 Limited, 2020).
Table 14.
Critical mineral inventories of porphyry copper-(molybdenum) deposits based on concentrations in anode copper and reserve tonnages.[Mt, million metric tons; wt %, weight percent; ppm, parts per million; t, metric tons; est., estimated; USGS, U.S. Geological Survey.]
Cu refinery (operator) | Ore source | Reserve/ production (Mt) | Years | Range of concentrations of Cu, monitored elements, and critical minerals in anode Cu | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cu (wt %) | Ag | Au | S | Se | Sb | As | Bi | Fe | |||||
(ppm) | |||||||||||||
Amarillo, Tex. (ASARCO) | ASARCO mines, Ariz. | Est. 700 | 1986/ 2018 | 98.6–99.51 | 445–1,500 | NR–19.5 | 10–30 | 509–850 | 82–800 | 300–900 | 45–210 | 40–657 | |
Magna, Utah (Kennecott/ Rio Tinto) | Bingham mine, Utah | 552 | 1987/ 2014 | 99–99.6 | 403–500 | 34–60 | 20–38 | 500–784 | 30–150 | 560–4,000 | 33–679 | 10–28 | |
El Paso, Tex. (Phelps Dodge/ Freeport-McMoRan) | Freeport-McMoRan mines, Ariz. | 11,254 | 1987/ 2018 | 98.9–99.7 | 60–1,200 | 1–17 | 7–60 | 133–1,000 | 1–500 | 10–3,000 | 5–200 | 1–100 | |
Miami, Ariz. (Cyprus/ Phelps Dodge) | Globe-Miami district mines, Ariz. | Unquantified refinery interim products | 1991/ 2003 | 99.5 | 400–510 | 2.5–94 | 10–18 | 300–320 | 100–270 | 80–770 | 12–20 | 12 | |
San Manuel, Ariz. (Magma Metals Co./ BHP) | San Manuel/ Kalamazoo mine, Ariz. | 797 | 1987/ 1998 | 99.7–99.8 | 175–375 | 8–21.3 | 18–20 | 410–450 | 39–73 | 24–616 | 3–70 | 14–15 | |
Amarillo, Tex. (ASARCO) | ASARCO mines, Ariz. | 148–1,700 | 80–500 | 10–50 (1,986) | 61–200 | 57,400–560,000 | 210,000–630,000 | 31,500–147,000 | 103,600–1,190,000 | 7,000–30,000 | 42,700–140,000 | Tables 9–11 | |
Magna, Utah (Kennecott/ Rio Tinto) | Bingham mine, Utah | 210–316 | 140–4,000 | NR | 60–150 | 16,560–82,800 | 309,120–2,208,000 | 18,216–374,800 | 115,920–174,432 | -- | 33,120–82,800 | Tables 9–11 | |
El Paso, Tex. (Phelps Dodge/ Freeport-McMoRan) | Freeport-McMoRan mines, Ariz. | 50–800 | 10–600 | NR | 10–190 | 11,254–5,627,000 | 112,540–33,762,000 | 562,700–2,250,800 | 562,700–9,003,200 | -- | 112,540–2,138,260 | Tables 9–11 | |
Miami, Ariz. (Cyprus/ Phelps Dodge) | Globe-Miami district mines, Ariz. | 377–600 | 90–129 | NR | 12–25 | -- | -- | -- | -- | -- | -- | Tables 9–11 | |
San Manuel, Ariz. (Magma Metals Co./ BHP) | San Manuel/ Kalamazoo mine, Ariz. | 68–121 | 31–63 | NR | 6–40 | 31,083–58,181 | 19,128–490,952 | 2,391–55,790 | 54,196–96,437 | -- | 4,782–31,880 | Tables 9–11; USGS (2013b) |
Table 15.
Estimated annual masses of critical minerals predicted in anode copper at operating copper refineries and not recovered (wasted) during production of anode copper at shuttered or demolished copper refineries, based on concentrations in anode copper, reserve tonnages, and mine life.[Mt, million metric tons; wt %, weight percent; yr, year; est, estimated; t, metric tons; %, percent; NR, not reported; USGS, U.S. Geological Survey.]