Critical Minerals in Subduction-related Magmatic-Hydrothermal Systems of the United States

Scientific Investigations Report 2023-5082
By: , and 

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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).

Figure 1. Five maps of deposits and resources of critical minerals distributed across
                     Western States.
Figure 1.

Maps showing locations of deposits and resources of critical minerals in Western States. A, Production (primary product; byproduct), reserves, and resources (including unmined deposits; mine, mill, and copper refinery interim products) of Sb, As, Bi, fluorite, Ga, Ge, In, Mn, potash, Te, Sn, Ti, and V in Western States (table 1). B, Porphyry copper-(molybdenum) (Cu-(Mo)) deposits in Western States. C, Porphyry Cu-Mo deposits and districts in Arizona and New Mexico. D, Porphyry Cu-Mo deposits and districts in Nevada. E, Tungsten deposits and resources in Western States and Alaska described in text and tabulated (open black diamonds; table 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.]

Deposit type Primary commodities; critical minerals Production of critical minerals in Western States Possible significant resources of critical minerals in Western States
Primary product, coproduct (chap. A) Byproduct (chap. B)1 Primary product, coproduct (chap. C) Byproduct (chap. C)
S-R-V tungsten W, Mo, Cu; W W: Pine Creek, Calif. Mo, Cu W: Andrew Curtis, Calif. --
W: Springer/ Nevada Massachusetts, Nev. -- W: Centennial, Nev. Au, Ag, Cu
W: Atolia, Calif -- W: Sunrise, Wash. Cu, Mo
W: Browns Lake, Mont. -- W: Pilot Mountain, Nev. Cu, Ag, Zn
-- -- W: Indian Springs, Nev. --
Porphyry/skarn copper Cu, Au, Ag, Mo; PGE, Te, Re, Co, Bi, U -- Te, PGE: Cu refineries and offsite Cu refinery, Magna, Utah Sb, As, Bi, Ge, In, Ni, PGE, Te: Cu refinery slimes2,3
-- PGE: Ely, Nev. Cu refinery, El Paso, Tex. Sb, As, Bi, Ge, In, Ni, PGE, Te: Cu refinery slimes2,3
-- PGE, Te: Bingham, Utah Cu refinery, Amarillo, Tex. Sb, As, Bi, Ge, In, Ni, PGE, Te: Cu refinery slimes2,3
-- Te: Butte, Mont. -- In: West Desert, Utah
-- Te: Amarillo, Tex. -- Te: Red Mountain, Ariz.4
-- -- -- Bi, Ge, In, Te: Sunnyside, Ariz.4
-- -- -- Re, PGE: Pebble, Alaska4
-- -- -- Ti (rutile): Bingham, Utah
-- -- -- Ti (rutile): Ajo, San Manuel, Bagdad, Ariz.
-- -- -- W: CuMo, Idaho
-- -- -- W: Margerie Glacier, Alaska
-- Re: Mo refineries --
-- Re: Bingham, Butte, Sierrita, Morenci, Bagdad, Santa Rita, others -- Re: Bingham, Butte, Sierrita, Morenci, Bagdad, Santa Rita. Other: Mo refineries
Polymetallic sulfide S-R-V-IS Cu, Zn, Cd, Pb, Ag, Au; Mn, Ge, Ga, In, Bi, Sb, As, W, Te V: St. Anthony mine, Mammoth, Ariz. Mn, Bi, As, Te: Butte, Mont. -- Mn: Hardshell-Alta-Hermosa, Ariz.
Bi: Leadville, Colo. Bi, Mn, Sb: Tintic, Utah -- --
-- Bi: Big, Little Cottonwood districts, Utah -- --
-- Bi?: Victoria, Nev. -- --
-- W, As: Gold Hill, Utah -- --
-- As: Eureka, Nev. (speiss) -- --
-- As: Battle Mountain district, Nev. -- --
-- Bi, Mn: Leadville, Colo. -- --
-- Mn: Gilman, Colo. -- --
-- Mn: Pioche-Bristol-Jackrabbit, Nev. -- --
-- Mn: Bisbee, Ariz. -- --
High-sulfidation gold-silver Au, Ag, Cu; As, Sb, Te, Bi, Sn, Ga -- -- -- Sb, As, Bi, Sn, Te, V: Goldfield, Nev.
-- -- -- Bi, Ga, Sb: Paradise Peak, Nev.
-- -- -- Sb, As, Bi, Te; Nevada-California districts
Lithocap alunite Al, K2SO4; Al, K2SO4, Ga Al, potash: Blawn Mountain, Utah -- Al, potash: Red Mountain, Ariz. --
Al, potash: Marysvale, Utah -- Al, potash: Sunnyside, Ariz. --
-- -- Al, potash: Resolution, Ariz. --
-- -- Al, potash: numerous deposits, Wash. --
Polymetallic sulfide S-R-V-IS Au, Ag, Pb, Zn, Cu; Ge, Ga, In, Bi, Te -- -- -- Te: Cripple Creek, Colo.
-- -- -- Te: Boulder district, Colo.
Porphyry/skarn
Polymetallic sulfide S-R-V-IS
Sn, W, Be; Sn, W, Be, Fluorite Cu, Sn: Majuba Hill, Nev. -- -- --
Cu, Zn, Pb, Ag, Au; Sn, Mn, Ge, Ga, In, Bi, Sb, As Sn: Temescal, Calif. -- -- --
-- Sn: Taylor Creek, N. Mex. -- Sn: Taylor Creek, N. Mex. --
Polymetallic, monometallic veins -- Sb: Yellow Pine, Idaho -- Sb: Yellow Pine, Idaho As, Bi, W: Yellow Pine, Idaho4
Sb: numerous districts, Nev. -- -- --
Sb: Coyote district, Utah -- Sb: Coyote district, Utah --
Sb, As: White Caps, Nev. -- -- --
Be, fluorite: Spor Mountain, Utah -- -- REE, Spor Mountain, Utah
Ge, Ga: Apex mine, Utah -- Ge, Ga: Apex mine, Utah --
-- -- Ga: Cordero/ McDermitt, Nev. --
Fluorite: Daisy mine, Nev. -- -- --
Fluorite: Baxter mine, Nev. -- -- --
Fluorite: Zuni Mountains, N. Mex. -- -- --
Fluorite: Lost Sheep mine, Utah -- -- --
Fluorite: Wagon Wheel Gap mine, Colo. -- -- --
-- -- Fluorite: McCullough Butte, Nev. --
-- -- -- Ti, Zr, Sn, White Mountains, Calif.
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.
1

Mining and (or) recovery enabled in part by subsidization, usually commodity price guarantees.

2

Includes mine waste (dumps, tailings, slag) and copper refinery slimes.

3

Calculated.

4

Inventory based on drill holes.

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.

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)
Table 2.    Characteristics of the largest tungsten deposits and resources in Western States.

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).

Figure 2. Spatial relationships of mineral systems and critical minerals.
Figure 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.

Figure 3. Combined imports and production of tungsten peaked in 1943.
Figure 3.

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 315). 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 1619). 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.]

Drill hole Depth (ft) Samples Au (ppb) Ag As Be Bi Cu Mn Mo Pb
from to (ppm)
BU-1 32 785 8 30.5 2.2 611.4 <5 5.1 3,058.4 -- 59.3 156.9
BB-2 40 140 10 46.1 4.4 207.0 -- 178.0 4,652.3 19.5 7.0 296.8
BB-3 14 90 8 18.1 4.8 98.1 -- 58.8 2,781.6 35.6 12.7 38.5
BB-3 600 720 12 51.9 3.2 157.5 -- 10.0 3,369.3 19.2 18.8 24.0
BB-4 12.6 200 19 43.5 3.6 411.3 -- 15.3 4,026.3 21.3 8.9 13.4
BB-6 20 120 10 23.2 8.6 476.0 -- 108.0 3,595.0 30.0 10.0 31.2
BB-6 300 490 19 49.9 12.8 1,568.4 -- 27.9 4,409.1 25.0 25.1 26.2
BB-2 to BB-6 average 78 38.8 6.2 486.4 <5 66.3 3,805.6 25.1 13.8 71.7
TM8 176 5,417 19 71.5 6.3 230.0 <5 48.5 3,150.1 -- 68.5 90.6
TR10 665 5,448 20 22.0 4.9 185.0 <5 2.2 3,118.2 -- 80.4 67.4
TM-13 3,900 4,040 14 23.9 8.5 102.5 0.5 11.4 585.3 3,677.5 97.6 1,197.2
TM-13 190 4,050 45 <104 1.5 17.1 <3 2.1 267.7 1,678.0 10.7 28,308.0
TM-14 540 4,580 95 21.6 0.9 42.3 -- -- 105.4 18.6 12.4 14.7
TM-14 n/a n/a n/a 17.6 0.9 31.0 -- 5.8 149.3 22.1 13.0 13.1
TM-14 n/a n/a n/a 16.7 1.8 64.2 -- 7.5 578.0 15.8 18.0 11.7
TM-14 n/a n/a n/a 12.6 0.7 103.9 -- 7.5 381.9 13.2 29.4 8.3
TM-14 n/a n/a n/a 14.4 1.6 32.0 -- 7.5 802.6 37.5 12.4 62.6
TM-14 4,400 4,580 19 8.3 2.1 63.1 -- 17.6 1,132.7 36.9 6.7 61.9
TM-14 540 4,580 114 15.2 1.3 56.1 <5 9.2 525.0 24.0 15.3 28.7
TCH-2 4,030 4,050 39 69.3 231.1 21.3 <3 652.4 5,464.2 11,235.1 10.7 18,708.4
4,653 4,949 -- -- -- -- -- -- -- -- -- --
TCH-2 4,109 5,300 61 <59 40.1 23.7 <9 225.1 2,587.9 10,828.9 68.9 7,826.7
TCH-2A 4,100 4,390 9 10.5 1.7 13.8 0.5 10.0 148.3 4,376.3 25.3 118.8
SU-2 241 802 3 29.7 4.0 1,296.7 <5 4.3 12,010.0 -- 138.0 321.7
4 DDH 180 2,735 11 76.7 34.5 210.0 <5 110.9 2,808.7 -- 19,841.7 887.2
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.

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.]

S (wt %) Sb V W Ga Ge In Li Ni Pd Pt Sn (ppm) Re (ppb) Te Zn
(ppm) (ppb) (ppm)
4.1 88.1 49.3 45.5 20.3 3.6 0.5 <10 64.8 1.0 1.2 15.8 -- -- --
4.1 28.0 1.9 -- -- -- -- -- -- -- -- -- -- -- --
3.8 12.5 1.4 -- -- -- -- -- -- -- -- -- -- -- --
2.5 5.0 2.8 -- -- -- -- -- -- -- -- -- -- -- --
3.0 26.4 2.2 -- -- -- -- -- -- -- -- -- -- -- --
4.7 87.5 1.9 -- -- -- -- -- -- -- -- -- -- -- --
5.0 92.4 1.9 -- -- -- -- -- -- -- -- -- -- -- --
3.8 42.0 2.0 <30 -- -- -- -- -- -- -- -- -- -- --
6.5 22.4 39.0 54.8 17.3 2.3 3.2 20.0 11.0 1.0 0.9 9.3 -- -- --
7.7 9.9 57.0 55.5 11.8 2.3 0.4 62.0 21.3 1.8 1.5 8.0 -- -- --
4.5 104.5 98.6 65.4 -- -- -- -- -- -- -- -- -- -- --
1.9 5.2 59.1 13.9 18.5 1 0.2 24.8 22.6 -- -- 3.6 36.2 0.7 556.1
3.9 7.5 3.9 -- -- -- -- -- -- -- -- -- -- -- --
5.5 9.4 2.2 -- -- -- -- -- -- -- -- -- -- -- --
3.8 22.5 1.5 -- -- -- -- -- -- -- -- -- -- -- --
4.9 20.4 2.7 -- -- -- -- -- -- -- -- -- -- -- --
3.7 11.1 3.1 -- -- -- -- -- -- -- -- -- -- -- --
4.2 12.7 3.7 -- -- -- -- -- -- -- -- -- -- -- --
4.3 13.9 2.8 <20 -- -- -- -- -- -- -- -- -- -- --
5.9 5.4 33.5 61.5 5.4 3.7 5.6 22.9 11.4 -- -- 5.2 19.4 29.8 96,282.5
-- -- -- -- -- -- -- -- -- -- -- -- -- -- --
1.4 9.9 243.9 0.4 8.7 1.8 1.5 45.6 19.0 -- -- 3.0 43.8 3.2 9,867.0
4.5 5.0 8.8 <30 -- -- -- -- -- -- -- -- -- -- --
17.6 161.3 80.3 61.3 12.0 2.0 <0.2 <10 18.7 1.0 2.0 13.7 -- -- --
10.4 21.1 87.4 123.4 17.9 3.7 2.2 <50 15.3 2.8 12.1 11.9 -- -- --
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.

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.]

Sample Recvd wt. (kg) Au Ag Ag (ppm) Al (wt %) As Ba Be Bi Ca (wt %) Cd Ce Co Cr Cs Cu Fe (wt %) Ga Ge
(ppm) (ppm) (ppm) (ppm)
WEI-21 ME-GRA21 ME-MS61
HDS-1A 0.06 <0.05 11 16.4 5.48 71.5 410 1.75 0.49 0.15 2.79 93 1 4 21.1 46.9 0.99 14.25 0.17
HDS-1B 0.05 <0.05 11 16.15 5.52 70.1 410 1.71 0.48 0.13 2.7 88.6 1 4 20 43.7 0.98 13.95 0.19
HDS-1C 0.06 <0.05 6 16.7 5.51 73 420 1.66 0.5 0.12 2.76 92.2 1 4 20.8 44.2 1 14.2 0.2
HDS-2A 0.06 <0.05 133 >100 2.13 2,880 350 0.88 0.67 1.68 26.3 32.6 5.9 22 3.04 1,195 4.03 15.05 0.11
HDS-2B 0.05 <0.05 142 >100 2.1 2,980 350 0.92 0.71 1.69 27.3 32.1 6.1 23 3.11 1,190 4.05 15.6 0.1
HDS-2C 0.04 0.13 125 >100 2.18 2,980 370 0.85 0.71 1.7 28.4 33.4 6.3 24 3.23 1,210 4.13 16.35 0.12
HDS-3A 0.06 0.07 147 >100 1.86 534 330 0.67 0.78 1.1 88.9 28.3 5.4 26 2.97 933 2.5 9.38 0.08
HDS-3B 0.05 0.11 138 >100 1.75 514 310 0.58 0.69 1.02 82.3 25.2 4.8 28 2.58 886 2.39 8.17 0.08
HDS-3C 0.06 0.1 144 >100 1.79 510 320 0.69 0.75 1.03 86 27.1 5.5 24 2.81 912 2.49 8.98 0.1
HDS-4A 0.05 0.13 391 >100 4.12 274 480 1.68 0.66 0.46 89.9 88.4 9.8 15 8.87 2,330 1.5 15.5 0.32
HDS-4B 0.06 <0.05 380 >100 4.17 281 490 1.42 0.66 0.47 90.3 89 9.7 14 8.9 2,280 1.47 15.45 0.29
HDS-4C 0.05 <0.05 393 >100 4.13 285 490 1.38 0.65 0.46 89.8 88.8 9.4 14 8.93 2,290 1.46 15.5 0.37
HDS-5A 0.06 0.26 1,105 >100 0.66 764 430 1.65 0.57 0.13 110 23.3 3.1 43 2.71 1,430 5.22 17.75 0.29
HDS-5B 0.06 0.19 1,075 >100 0.66 746 430 1.92 0.54 0.13 112.5 23.5 2.9 30 2.58 1,430 5.18 17.9 0.3
HDS-5C 0.06 0.2 1,000 >100 0.65 751 440 1.86 0.51 0.13 112 23.4 3.1 29 2.63 1,435 5.21 18.45 0.29
Average -- -- -- 16.4 -- 914.2 -- -- 0.6 -- -- -- 5.0 20.3 -- 1,177.1 -- 14.4 0.2
HDS-1A 6.1 0.24 0.063 3.09 44 15.1 0.34 1,555 -- 0.89 0.11 13 2.1 260 1,170 275 <0.002 0.01
HDS-1B 5.9 0.24 0.062 3.02 42.6 14.7 0.33 1,575 -- 0.77 0.1 12.7 2 250 1,160 269 <0.002 0.01
HDS-1C 6.1 0.24 0.063 3.08 43.9 15.4 0.34 1,595 -- 0.87 0.11 13.2 2.4 270 1,190 274 <0.002 0.01
HDS-2A 1.7 0.21 0.209 1.32 16.1 18.4 0.04 29,000 2.9 4.45 0.02 2.1 2.4 940 >10,000 79.7 0.002 0.08
HDS-2B 1.7 0.2 0.213 1.27 15.9 18.8 0.04 29,800 3 4.85 0.02 2.5 2.6 940 >10,000 82.2 0.002 0.08
HDS-2C 1.8 0.19 0.226 1.35 16.6 20 0.04 29,800 3 4.84 0.02 2.7 2.8 950 >10,000 87.8 0.002 0.08
HDS-3A 1.8 0.39 0.138 1.22 14 21.5 0.05 24,900 2.5 4.22 0.02 2.1 3.2 740 >10,000 84.4 0.002 0.08
HDS-3B 1.6 0.42 0.119 1.13 12.4 18.7 0.04 24,100 2.4 4.3 0.02 2.2 2.8 720 >10,000 72.1 <0.002 0.08
HDS-3C 1.7 0.43 0.135 1.17 13.4 21.1 0.04 24,400 2.4 3.63 0.02 1.9 3.1 710 >10,000 79.1 0.002 0.08
HDS-4A 4.1 0.56 0.195 2.02 34.1 16.5 <0.01 90,500 9.1 5.4 0.03 9 8.8 390 >10,000 149.5 <0.002 0.05
HDS-4B 4.2 0.56 0.204 1.99 34.4 16 <0.01 90,600 9.1 5.33 0.03 8.8 8.7 390 >10,000 150.5 <0.002 0.05
HDS-4C 4 0.68 0.2 2 33.9 15.1 <0.01 89,200 8.9 5.4 0.03 8.7 8.1 380 >10,000 148 0.002 0.05
HDS-5A 1.6 0.68 0.139 0.67 13.4 21 <0.01 95,400 9.5 13.2 0.02 4.9 20.5 260 >10,000 39.3 <0.002 0.06
HDS-5B 1.3 0.68 0.119 0.67 13.7 19.9 <0.01 97,100 9.7 10.1 0.02 4.3 19.1 260 >10,000 36.2 <0.002 0.06
HDS-5C 1.3 0.6 0.136 0.68 13.5 21.2 <0.01 97,000 9.7 10.15 0.02 4.7 19.6 270 >10,000 37.2 <0.002 0.06
Average -- -- 0.1 -- -- 18.2 -- 48,435.0 -- 5.2 -- 6.2 7.2 -- 1.173.3 124.3 0.0 --
HDS-1A 77.9 5.3 4 2 33.9 0.83 0.2 12.3 0.157 3.01 4.4 17 1.9 31.2 284 164 -- -- --
HDS-1B 75.7 5 4 1.9 32.3 0.83 0.18 12.1 0.155 2.91 4.2 16 1.9 29.5 281 159.5 -- -- --
HDS-1C 76.6 5.3 3 2 33.5 0.87 0.18 12.3 0.159 3.05 4.4 16 2 30.6 289 165 -- -- --
HDS-2A 1,965 3.3 6 2.1 26.7 <0.05 7.31 4.1 0.128 4.45 5.1 38 8.3 11.9 1,900 53.1 152 3.92 --
HDS-2B 2,040 3.4 6 2.2 27.4 0.05 7.68 4 0.127 4.55 5.2 38 9.4 12.2 1,850 53.6 155 3.86 --
HDS-2C 2,130 3.5 6 2.2 28.7 0.05 8.05 4.2 0.133 4.84 5.4 39 9.8 12.5 1,880 56.9 149 3.83 --
HDS-3A 1,590 2.9 4 1.2 35.3 <0.05 2.48 3.6 0.121 5.68 3.9 34 4.2 11.9 3,310 54.1 225 2.15 --
HDS-3B 1,560 2.5 4 1.1 31.1 <0.05 2.32 3.2 0.116 4.97 3.4 34 4.1 10.4 3,140 47 229 2.19 --
HDS-3C 1,555 2.7 4 1.2 33.4 <0.05 2.43 3.6 0.119 5.47 3.8 34 4 11.4 3,220 50.9 224 2.17 --
HDS-4A 457 4 7 2 39.2 0.6 0.98 7.8 0.164 16.15 6.1 48 8.9 25.9 >10,000 113.5 451 1.69 1.07
HDS-4B 461 4 5 1.9 38.9 0.59 0.82 8.1 0.164 16.95 6.3 48 8.9 23.7 >10,000 102.5 455 1.72 1.08
HDS-4C 461 4.3 5 1.9 38.6 0.61 0.76 8.2 0.164 16.55 6.4 48 8.7 23.3 >10,000 103 451 1.7 1.08
HDS-5A 1,275 0.8 4 3.6 102.5 0.37 6.98 2 0.144 28.9 7.7 23 28.5 14 7,750 49.4 1,330 6.91 --
HDS-5B 1,265 0.6 3 3 102.5 0.31 6.12 2 0.144 28.5 7.6 23 27.6 14.3 7,830 49.8 1,240 6.23 --
HDS-5C 1,270 1.1 4 3 103.5 0.35 7.4 2.1 0.143 29.6 8 23 27.8 14.6 7,820 40.3 1,230 6.21 --
Average 1,083.9 -- -- 2.1 -- -- 3.6 -- -- -- -- 31.9 -- -- 3,296.2 -- -- -- --
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.

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.]

Ag Al As Au Be Bi Cu Ga Ge In Li Mn Mo
(ppm)
1.30 75,370.85 41.48 0.27 1.36 1.20 2,897.28 19.26 0.17 0.05 16.76 446.71 203.35
15.31 22.31 0.02 0.00 0.35 24,616.06 3.89 8.71 1.67 0.40 0.62 222.05 13.00
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.

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.]

Intervals averaged Ag
(MS-HF)
Ag
(AA-F-AE-P)
Al
(wt %)
As Be Bi Cu
(AES-HF)
Cu
(AA-F-AE-P)
Ga Ge In K
(wt %)
Mn
(ppm) (ppm) (ppm)
~10,930 (total dataset) 2.65 -- 6.51 4.02 2.08 2.14 748.04 -- 18.88 0.12 0.06 3.41 218.05
2,261 with Cu >1,000 ppm 5.76 -- 6.56 5.77 2.14 3.25 1,627.17 -- 19.34 0.13 0.12 3.43 201.85
835 with Cu >1,000 ppm -- 4.33 -- -- -- -- -- 1,642.19 -- -- -- -- --
~10,930 (total dataset) 313.76 -- 5.18 27.57 0.02 0.26 0.64 1.85 5.24 0.86 0.23 17.27 40.22 --
2,261 with Cu >1,000 ppm 294.05 -- 5.16 -- 0.01 0.41 1.07 2.73 7.03 0.84 0.37 18.63 60.55 --
835 with Cu >1,000 ppm -- 327.97 -- -- -- -- -- -- -- -- -- -- -- 46.82
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.

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]

Resource Mass Composite Depth (ft) Sb As Bi W
(g/t)
Hangar Flats resource -- 8 DDH 3–1,014 10,473.8 27,791.2 5,138.9 317.3
West End resource -- 9 DDH 85–935 241.4 12,974.9 1,916.5 86.0
Yellow Pine resource -- 2 DDH 78–392 6,326.9 19,717.6 4,192.9 46.2
Average concentration -- -- -- 5,681 20,161 3,749 150
Total resource tonnage1 104 Mt -- -- 59,082 209,673 38,989 1,560
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.
1

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.]

Au (ppb) Au (opt) F (ppm) Hg (ppb) Ag (ppm) Al (wt %) As Ba Be Bi Ca (wt %) Cd Ce Co Cr Cs Cu
(ppm) (ppm)
MS61
1,155.2 BLD 1,448.3 BLD BLD BLD 132.4 BLD BLD 1.0 BLD BLD BLD 9.8 39.7 BLD 35.9
BLD 25.6 0.4 BLD 0.1 BLD BLD 39.6 BLD 1,005.5 47.7 BLD BLD 28.6 BLD 124.3 167.8
BLD BLD 8.9 BLD 10.7 637.7 BLD 4.8 BLD 0.4 BLD BLD 118.8 25.0 BLD 206.5 170.3
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.

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 9.    Compositions of anode copper from domestic copper smelters, 1986–2018.

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 10.    Compositions of tank house slimes from domestic copper refineries, 1986-2018.

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.]

Year Sample source Refinery location Sample analyzed Cu (wt %) Au (wt %) Au (ppm) Au (opt) Ag (wt %) Ag (ppm) Ag (opt) Au+Ag (ppm)
1897 Not provided Not provided Blister Cu1
[Subsample:
bottom-
center-
top of “ingot block”]
-- -- 0.68-
10.9-
0.89
-- -- 2,480-
6,410-
4,540
-- --
1899 Copper Queen mine, Bisbee district, Ariz. Douglas, Ariz.? Matte Cu2 50.5–98.9 -- -- -- -- -- -- --
1911 Copper Queen mine, Bisbee district, Ariz. Douglas, Ariz.? Matte Cu2 -- 0.0035 35 -- 0.02 200 -- --
Butte district, Mont. Great Falls reduction plant, Mont. Matte Cu -- 0.0003 0.3 -- 0.05 500 -- --
Anode mud -- 0.05–1 500–10,000 -- 23 230,000 -- --
1914 Mostly Bingham, Utah, Cu ore Garfield, Utah 5,000 short tons blister Cu3 -- -- -- 2.88 -- -- 34.80 --
Ely, Nev., Cu ore Ely (Steptoe), Nev. 3,000 short tons blister Cu3 -- -- -- 1.69 -- -- 5.50 --
Cu-Pb mattes from several Pb-Ag refineries Omaha, Nebr. 800 short tons blister Cu3 -- -- -- 3.50 -- -- 230.90 --
Not provided Mountain, Calif. 150 short tons blister Cu3 -- -- -- 14.18 -- -- 109.90 --
Pacific coast and Alaska Cu ores Tacoma, Wash. 800 short tons blister Cu3 -- -- -- 21.67 -- -- 67.10 --
1914 Butte, primarily; in mid-1950s ~30,000 short tons per year cement Cu from Yerington, Nev., were refined; small amounts of matte Cu and speiss received from International Smelting and Refining at Tooele, Utah; increased Se (1957) from Tooele products; Sb varied with converter used Great Falls reduction plant, Mont. Anode Cu4 99.13 -- -- -- -- -- -- 1,380
1926 Anode Cu4 99.28 -- -- -- -- -- -- 2,410
1929 Anode Cu4 99.30 -- -- -- -- -- -- 2,130
1957 Anode Cu4 99.55 -- -- -- -- -- -- 960
1934 Not provided Raritan Copper Works, Perth Amboy, N.J. Raw slime 18.10 -- -- 101.52 -- -- 5,131 --
Treated slime5 1.74 -- -- 146.2 -- -- 7,684 --
1954 Baltimore, Md. Baltimore, Md. -- 99.43 -- 1.41 -- -- 18.7 -- --
Raritan, N.J. Perth-Amboy, N.J. -- 99+ -- 1.5 -- -- 55 -- --
Tacoma, Wash. Tacoma, Wash. -- 98.08 -- 3.59 -- -- 90.2 -- --
Anaconda, Mont. Great Falls, Mont. -- 99.45 -- 0.32 -- -- 46.72 -- --
1973 Bingham, Utah, Cu ore Magna, Utah Anode mud 30 -- -- 290 -- -- 2,900 --
Table 11.    Copper and minor element concentrations in matte and blister copper and tank house slimes of domestic copper refineries, 1897–1973.
1

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.

2

Matte Cu (30–70%) is produced by initial melting of concentrate and gravitational removal of silicate slag.

3

Element concentrations calculated from tabulated bulk analyses.

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 11.    Copper and minor element concentrations in matte and blister copper and tank house slimes of domestic copper refineries, 1897–1973.
4

Anode Cu (99%) is produced by removing remaining S, Fe, and O from blister Cu; it is cast into sheets for further purification (to cathode Cu) by electrolysis.

5

Boiled, washed, and filtered.

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.]

Porphyry Cu-(Mo) system Deposit domain Resource
(Mt)
Reserve
(Mt)
Number of analyses Concentrations of primary, coproduct, and byproduct commodities
Cu Mo Pb Zn Au Ag Mn
(wt %) (ppm) (wt %)
Pebble, Alaska Cu-Mo-Ag-Au-mineralized gd 7,510 -- 7,520 0.41 0.024 0.002 NR 0.33 1.3 --
CuMo, Idaho (>0.1 wt % Cu) Cu-Mo-Ag-mineralized rocks ~2,270 -- 10,930 0.16 0.03 -- -- -- 5.7 --
Red Mountain, Ariz. Deep cpy-bn porphyry 385 -- 300 0.58 0.009 -- -- 0.004 0.12 --
Near surface cc-en 100–150 -- 0.31 0.02 -- -- -- -- --
Sunnyside, Ariz. Deep cpy porphyry 1,500 -- 95 0.33 0.011 -- -- <0.002 0.16 --
Near-surface cc-en-tn 800 -- 97 0.175 <0.01 -- -- <0.07 0.23 --
Deep polymetallic replacement NR -- 100 0.4 <0.01 13.3 5.3 0.07 136.5 0.44
Hardshell-Alta-Hermosa, Ariz. Polymetallic replacement -- -- 15 0.12 0.05 0.12 0.03 <0.26 347 4.84
Clark deposit 33 -- -- -- -- -- 2.31 -- 78 9.08
Ventura, Ariz. Mo-Cu breccia pipe 3.6 -- 11 2.4 2.4 0.89 NR 0.080 35 --
Bingham, Utah Cu-Mo porphyry -- 552 -- 0.44 0.031 -- -- 0.16 2.11 --
Cu-Mo porphyry 285 -- -- 0.38 0.017 -- -- 0.2 1.79 --
North Rim skarn 20 -- -- 3.65 -- -- -- 1.62 20.95 --
Cu-Mo ore 285 552 -- 0.69 0.106 -- -- 0.41 4.9 --
Mo core -- -- -- 0.14 0.096 -- -- 0.13 0.9 --
Barren core -- -- -- 0.06 0.012 -- -- 0.14 0.6 --
Ore stockpile -- 0.2 90 -- -- -- -- -- -- --
Yerington, Nev. Ann Mason Cu porphyry 2,219 -- 30 0.29 Est. 0.007 -- -- -- 0.66 --
MacArthur Cu porphyry 159 -- 1,000 0.21 -- -- -- -- -- --
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.

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 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.
1

Values in parentheses are average concentrations.

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)
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.
1

Critical mineral resources calculated using concentrations in diamond drill hole intercepts and an estimated tonnage.

2

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 911
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 911
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 911
Miami, Ariz. (Cyprus/ Phelps Dodge) Globe-Miami district mines, Ariz. 377–600 90–129 NR 12–25 -- -- -- -- -- -- Tables 911
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 911; USGS (2013b)
Table 14.    Critical mineral inventories of porphyry copper-(molybdenum) deposits based on concentrations in anode copper and reserve tonnages.

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.]

Cu refinery (operator) Ore source Mine reserves and forecasted production
Reserve (Mt) Production (Mt) Cu (wt %) Mine life (yr) Total Cu (reserves, production) (Mt) Est. Cu/yr (t) Est. % Cu production/ yr
Amarillo, Tex. (ASARCO) Mission complex (2016) 303.4 -- 0.42 12 1,274,280 106,190 52
Ray (2018; sulfide, mill ore) 444.7 -- 0.514 23 2,285,758 99,381 48
Silver Bell (2009) 141.4 -- 0.33 -- 466,620 -- --
Magna, Utah (Kennecott/Rio Tinto) Bingham mine, Utah 552 -- 0.44 11 2,428,800 220,800 --
El Paso, Tex. (Phelps Dodge/ Freeport-McMoRan) North America: Morenci, Bagdad, Safford, Sierrita, Miami, Ariz.; Chino, Tyrone, N.Mex. 11,254 -- -- 1Est. 16.6 23,550 11,418,000 --
Morenci 4,300 -- 0.23 -- 6,500 -- --
Sierrita 3,240 -- 0.22 -- 6,000 -- --
Bagdad 2,591 --