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Minerals & deposits

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USGS2018

Application of imaging spectroscopy for mineral exploration in Alaska: A study over porphyry Cu deposits in the eastern Alaska Range

The U.S. Geological Survey tested the utility of imaging spectroscopy (also referred to as hyperspectral remote sensing) as an aid to regional mineral exploration efforts in remote parts of Alaska. Airborne imaging spectrometer data were collected in 2014 over unmined porphyry Cu deposits in the eastern Alaska Range using the HyMap™ sensor. Maps of the distributions of predominant minerals, made by matching reflectance signatures in the remotely sensed data to reference spectra in the shortwave infrared region, do not uniquely discriminate individual rock units. However, they do highlight hydrothermal alteration associated with porphyry deposits and prospects hosted mostly within the Nabesna pluton. In and around porphyry Cu deposits at Orange Hill and Bond Creek, unique spectral signatures are related to variations in chlorite and white mica abundance and their chemical composition. This is best revealed in the longer-wavelength 2,200-nm Al-OH absorption feature positions in pixels spectrally dominated by white mica proximal to porphyry deposits. Similar spectral signatures of chlorite and white mica wavelength positions were also recognized away from the porphyry deposits; follow-up sampling identified these satellite areas to also contain Cu-Mo-Au mineralized rock. Our study confirms that airborne imaging spectroscopy has application for regional mineral exploration in exposed mountainous terrain in Alaska.

Alaska↗

USGS2019

Magmatic-hydrothermal gold mineralization at the Lone Tree Mine, Battle Mountain district, Nevada

The Lone Tree deposit is located in the northern Battle Mountain mining district, Nevada. Prior to mine closure in 2006, Santa Fe Pacific Gold and Newmont produced 4.2 Moz of gold at an average grade of 2.06 g/t at Lone Tree, primarily from the N-S– to NNW-SSE–striking Wayne zone. The ore is located between the Roberts Mountain and Golconda thrusts in siliciclastic rocks of the Ordovician Valmy Formation and in the Pennsylvanian-Permian Battle Mountain and Edna Mountain Formations, and above the Golconda thrust in siliciclastic and carbonate rocks of the Mississippian to Permian Havallah sequence. Ore is also hosted by rhyolitic dikes that were emplaced at 40.95 ± 0.06 Ma based on zircon U-Pb chemical abrasion-thermal ionization mass spectrometry. The gold is associated with sericitic and argillic alteration of the siliciclastic rocks and dikes and with decarbonatization and Fe carbonate alteration of the carbonate-bearing units, as well as in Fe-As sulfide and finegrained quartz alteration of all rock types. Oxidation affects 30 to 45% of the deposit, penetrating into the stratigraphy along numerous steeply dipping north-south, east-west, and north-northeast–south-southwest structures. Gold is positively correlated with Ag, As, Hg, and Sb. The highest Au grades occur in quartz-sulfide ore hosted in siliciclastic and carbonate sedimentary rocks and rhyolitic intrusions. In this ore style, fine-grained quartz and sericite are intergrown with disseminated sulfide minerals (quartz-sericite-pyrite alteration), constituting cores of weakly mineralized pyrite or marcasite, which are surrounded by fuzzy arsenopyrite rims that contain up to ~2,000 ppm Au. Low gold grades occur in late-stage banded pyrite breccias consisting of a finely zoned Au-poor pyrite matrix surrounding jigsaw-fit clasts of quartz-, illite-, barite-, and adularia-altered siliciclastic rock. The timing of main-stage mineralization is bracketed between the emplacement of the dikes and an adularia 40 Ar/ 39 Ar age of 40.14 ± 0.74 Ma. Sericite intergrown with arsenopyrite-rimmed pyrite in phenocrysts of the rhyolite dikes gave δ 18 O values of 1.6 to 9.5‰ and δ D values of –105 to –145‰. For temperatures of 300 ± 100°C, the calculated fluid isotopic compositions are consistent with felsic magmatic water and minor modifications by mixing with meteoric water and exchange with wall rocks. In the silica-sulfide ore, in situ isotopic laser ablation-multicollector-inductively coupled plasma-mass spectrometry (LA-MC-ICP-MS) analyses of pyrite cores yielded δ 34 S values ranging from 3.4 to 7.7‰, with average values of 5.6‰ in the felsic dikes, 4.5‰ in the siliciclastic rocks, and 5.3‰ in the carbonate rocks. These values match conventional pyrite δ 34 S data reported for Eocene porphyry systems elsewhere in the district. Nanoscale secondary ion mass spectrometry analyses show that gold and associated trace elements occur in submicron-scale zones within arsenopyrite rims on pyrite. The average δ 34 S values of the arsenopyrite rims are 5.3 to 6.5‰ heavier than the pyrite cores, indicating cooling and an increasing H 2 S/SO 2 ratio. The highest grades resulted from episodic pulses of a gold-rich fluid that was partly derived from, or exchanged with, the sedimentary host rocks. In situ LA-MC-ICP-MS δ 34 S values for the late-stage banded pyrite breccia become progressively lighter from veinlet margin to center, reaching a low of –32‰. These veinlets indicate a shift from main-stage quartz-sericite-pyrite and intermediate argillic alteration to more neutral pH and oxidizing conditions during late-stage mineralization, indicating either increasing interaction between the fluid and sedimentary sulfur sources in the host-rock package or bacterial sulfate reduction and supergene sulfide precipitation.

Nevada↗

USGS2021

Paragenesis of an orogenic gold deposit: New insights on mineralizing processes at the Grass Valley District, California

The Grass Valley orogenic gold district in the Sierra Nevada foothills province, central California, is the largest historical gold producer of the North American Cordillera. Gold mineralization is associated with shallowly dipping north-south veins hosted by the 160 Ma Grass Valley granodiorite to the southwest of the Grass Valley fault and steeply dipping east-west veins in accreted oceanic rocks to the northeast of this major fault. Quartz veins from both vein types show well-preserved primary textural relationships. Using a combination of petrographic and microanalytical techniques, the paragenetic sequence of minerals within the veins and the compositions of ore minerals were determined to constrain the mechanisms of quartz vein formation and gold deposition. The veins are composed of early quartz that formed through cooling of hydrothermal fluids derived from a geopressured reservoir at depth. The early quartz shows growth zoning in optical cathodoluminescence and contains abundant growth bands of primary inclusions. The primary inclusion assemblages and myriads of crosscutting secondary fluid inclusions have been affected by postentrapment modification, suggesting that early quartz formation was postdated by pronounced pressure fluctuations. These pressure fluctuations, presumably involving changes from lithostatic to hydrostatic conditions, may be related to fault failure of the host structure as predicted by the fault-valve model. Fluid flow associated with pressure cycling took place along microfractures and grain boundaries resulting in extensive recrystallization of the early quartz. Deposition of pyrite, arsenopyrite, and first-generation gold from these hydrothermal fluids causing recrystallization of the early quartz occurred as a result of wall-rock sulfidation. The gold forms invisible gold in the compositionally zoned pyrite or micron-sized inclusions within pyrite growth zones. The latest growth zones in euhedral quartz crystals that formed in association with this stage of the paragenesis contain very rare primary fluid inclusions that have not been affected by postentrapment modification. The hydrothermal system transitioned entirely to hydrostatic conditions immediately after formation of the latest quartz, explaining the preservation of the primary fluid inclusions. The formation of minor quartz in open spaces was followed by the deposition of second-generation native gold and telluride minerals that are commonly associated with base metal sulfides. Ore formation at this stage of the paragenesis is attributed to the rapid decompression of hydrothermal fluids escaping from the geopressured part of the crust into the overlying hydrostatic realm. There is no fluid inclusion evidence that this pressure drop resulted in fluid immiscibility of the hydrothermal fluids. Fluid inclusion evidence suggests that the north-south veins formed at a paleodepth of ~8 km, whereas the east-west veins appear to have formed at ~10 to 11 km below surface, confirming previous inferences that the NE-dipping Grass Valley reverse fault accommodated a large displacement. The findings of the study at Grass Valley have significant implications for the model for orogenic gold deposits, as the reconstruction of the paragenetic relationships provides evidence for the occurrence of two discrete events of gold introduction that occurred at different conditions during the evolution of the hydrothermal system.

California↗

USGS1997

Geologic setting and characteristic of mineral deposits in the central Wasatch Mountains, Utah

Base- and precious-metal deposits in the central Wasatch Mountains southeast of Salt Lake City were mined for more than 100 years beginning in 1868. Deposits present in the Park City, Little Cottonwood, and Big Cottonwood mining districts include Ag-Pb-Zn ± Cu ± Au replacements and veins, a low-grade porphyry Cu-Au deposit, Cu-bearing skarns, a quartz monzonite-type (low F) porphyry Mo deposit, and high sulfidation (quartz-alunite) Au deposits. Most production came from polymetallic replacement and vein deposits in the Park City mining district, which has a recorded production of more than 1.4 million oz Au, 253 million oz Ag, 2.7 billion lbs Pb, 1.5 billion lbs Zn, and 129 million lbs Cu from 1872 to 1978. Production in the Little and Big Cottonwood districts, mostly from Pb-Ag replacement deposits, was much smaller. Most mineral deposits in the central Wasatch Mountains are genetically related to the Wasatch igneous belt, a series of high-K calc-alkaline stocks and cogenetic volcanic rocks that formed about 41(?) to 30 Ma. The mineral deposits mostly formed near the end of magmatic activity between about 36 to 31.4 Ma. A subeconomic porphyry Mo deposit in the Little Cottonwood stock is notably younger having formed about 26 to 23.5 Ma. The intrusive rocks were emplaced mostly along the westward extension of the west-trending Uinta arch during a period of NW-SE-directed extension, and much of the mineralization in the Park City district was controlled by ENE-striking normal faults. About 15 degrees of eastward tilting of the central Wasatch Mountains during Late Cenozoic Basin and Range extension has resulted in progressively deeper levels of exposure from <1 km on the east to about 11 km on the west and in profound variations in the types of mineral deposits exposed in different parts of the range. Most deposits formed at paleodepths ≤5 km, and the most productive deposits in the Park City district formed at depths of 1 to 2 km. The porphyry Mo deposit in the Little Cottonwood stock formed at greater depths of about 6 km.

Utah↗

USGS1997

New K-Ar and 40Ar/39Ar ages of plutonism, hydrothermal alteration, and mineralization in the central Wasatch Mountains, Utah

Twenty-one new K-Ar and 10 new 40 Ar/ 39 Ar ages are reported for igneous and hydrothermal minerals from intrusive rocks of the Wasatch igneous belt in the central Wasatch Mountains. Interpretation of our new data combined with previously published K-Ar ages and with new 40 Ar/ 39 Ar and U-Pb ages reported by Vogel et al. (1997) suggests that the Clayton Peak stock was emplaced at about 36 to 35 Ma, the Alta stock at about 35 to 33 Ma, and the Little Cottonwood stock at about 31 to 30 Ma. Biotite K-Ar ages progressively increase from west to east in the Little Cottonwood stock, which is consistent with more rapid cooling of the eastern part of the stock and with other evidence suggesting about 15 degrees of eastward tilting of the central Wasatch Mountains following emplacement of the Wasatch igneous belt. Most porphyry stocks in the Park City mining district were emplaced at about 41 to 40 Ma; the Ontario stock was emplaced at about 36 Ma. Vein deposits in the Park City mining district formed at about 36 to 33 Ma. The Park Premier stock was emplaced in several pulses between about 35 to 32 Ma. Alteration related to porphyry copper mineralization in the Park Premier stock formed at 33.5 Ma and advanced argillic alteration and gold mineralization formed at 31.4 Ma. Molybdenum mineralization in the eastern part of the Little Cottonwood stock formed between 26 to 23.5 Ma.

Utah↗

USGS2018

Chapter 10: Regional- to deposit-scale geologic controls on copper-silver mineralization in the Kalahari Copperbelt, Botswana

The Kalahari Copperbelt in northwestern Botswana is characterized by structurally controlled, stratabound, mineralogically zoned copper-silver deposits hosted along a major redox boundary within a late Mesoproterozoic rift succession. Copper-silver mineralized rocks occur on the limbs and in the hinge positions of regional-scale folds that characterize the Pan-African Ghanzi-Chobe zone fold-and-thrust belt. Regional facies changes along the base of the transgressive marine D’Kar Formation, the host to the majority of mineralized rocks, delineate a series of synsedimentary basin highs and lows. The facies changes were identified through both lithostratigraphic analysis of drill holes and along-strike variations in magnetic lithostratigraphy, a technique that correlates the magnetic fabrics of second vertical derivative aeromagnetic maps with changes in lithostratigraphy. Basin highs controlled the development and distribution of favorable lithostratigraphic and lithogeochemical trap sites for later sulfide precipitation. Major facies changes across the Ghanzi Ridge area straddle a significant crustal structure identified in gravity datasets that appears to have influenced extensional activity during basin development. During basin inversion, the basin highs, cored by rheologically stronger bimodal volcanic rocks, localized strain within mechanically weaker rock types of the Ghanzi Group metasedimentary rocks, leading to the development of locally significant permeability and the formation of structural trap sites for mineralization by hot (250°–300°C), oxidizing, metalliferous Na-Ca-Cl brines. Structural permeability was maintained within trap sites due to silicification and/or feldspar alteration during progressive deformation and associated hydrothermal mineralizing events.

Kalahari Copperbelt↗

USGS1984

SURVEY OF ASBESTOS-RELATED DISEASES IN TRADES AND MINING OCCUPATIONS AND IN FACTORY AND MINING COMMUNITIES AS A MEANS OF PREDICTING HEALTH RISKS OF NONOCCUPATIONAL EXPOSURE TO FIBROUS MINERALS.

A review based on 36 published epidemiological studies is given of disease patterns that have developed among industrial workers, miners, and millers who had been exposed to dusts of one or more of the commercial asbestos minerals or to dusts from minerals perceived to be asbestos-like. Health data are also reviewed for individuals exposed to asbestos dusts in nonoccupational settings. From the published reports it is clear that there are very significant differences in the health effects of the several asbestos or asbestos-like minerals.

Conference Paper↗

USGS1984

A new occurrence of telluride minerals in South Carolina

A study of drill cores from the Haile gold mine, Lancaster County, South Carolina, has revealed grains containing large amounts of Te with various combinations of Pb, Ag and Au in pyrite. These telluride minerals have so far not been identified. The nearby Brewer mine, on the basis of chemical evidence, also contains tellurides. The probable telluride localities in South Carolina are now expanded to three, significantly increasing the few reports of Te minerals from the Au deposits of the southeastern Piedmont, many of which are now considered to be volcanogenic. The occurrence of telluride minerals in gold ore from the Haile-Brewer area may help to explain the divergence in Au/Ag ratios reported in chemical analyses of drill core, ore samples and production records. Te, in addition, may be useful in geochemical exploration programmes in the SE Piedmont, including programmes using heavy mineral concentrates derived from stream alluvium. -R.S.M.

South Carolina↗

USGS1987

Nature and distribution of potential heavy-mineral resources offshore of the Atlantic Coast of the United States.

The US is dependent on foreign imports of placer heavy minerals for a majority of its ilmenite and rutile, and virtually all of its monazite requirements. Although sand deposits in the SE US are important domestic sources of these heavy minerals (HM) and a number of other less well-known heavy-mineral species, global onshore reserves of placer minerals may fall short of demand in as few as 20 years. Insofar as they are important commodities for the future, offshore HM placers will become more important, but much research on them remains to be done. Results of recent offshore studies, based on surficial grab samples, indicate an average of about 2 weight percent HM in surficial Atlantic Continental Shelf (ACS) sediments, in strong contrast with previous estimates of an average of 0.16% HM. Although provocative, the information from these grab samples does not include the thickness of the HM deposits and thus their volume and tonnage cannot be estimated.-from Author

Marine Mining↗

USGS1989

Availability of a library of infrared (2.1-25.0 μm) mineral spectra

All previously published libraries of infrared mineral spectra are in the form of transmittance. Reflectance spectra are, however, more useful for remote sensing and some potential laboratory applications, such as the use of an infrared microscope for mineral identification on polished sections. This note points out that construction of a new library of infrared (2.1-25.0 μ m) mineral spectra is in progress. Both transmittance and reflectance measurements of a selection of 63 different, well-characteized minerals have been published to date. These data are available in both hard copy and digital form.

American Mineralogist↗

USGS2014

The role of conflict minerals, artisanal mining, and informal trading networks in African intrastate and regional conflicts

The relationship between natural resources and armed conflict gained public and political attention in the 1990s, when it became evident that the mining and trading of diamonds were connected with brutal rebellions in several African nations. Easily extracted resources such as alluvial diamonds and gold have been and continue to be exploited by rebel groups to fund their activities. Artisanal and small-scale miners operating under a quasi-legal status often mine these mineral deposits. While many African countries have legalized artisanal mining and established flow chains through which production is intended to travel, informal trading networks frequently emerge in which miners seek to evade taxes and fees by selling to unauthorized buyers. These networks have the potential to become international in scope, with actors operating in multiple countries. The lack of government control over the artisanal mining sector and the prominence of informal trade networks can have severe social, political, and economic consequences. In the past, mineral extraction fuelled violent civil wars in Sierra Leone, Liberia, and Angola, and it continues to do so today in several other countries. The significant influence of the informal network that surrounds artisanal mining is therefore an important security concern that can extend across borders and have far-reaching impacts.

Small Wars Journal↗

USGS1976

Halogen contents of igneous minerals as indicators of magmatic evolution of rocks associated with the Ray porphyry copper deposit, Arizona

The contents of Cl, F, and H 2 O+ (calculated) in some hydrous igneous minerals in intrusive rocks of Laramide age (70-60 m.y.) near Ray, Ariz., appear to be related to the age and the chemistry of the whole-rock samples. Apatite and biotite in younger, more silicic rocks contain more F but less Cl and H 2 O+ than apatite and biotite in older, more mafic rock; the same relations hold for F and H 2 O+ in sphene. Correlations of the abundance of Cl, F, and H 2 O+ in hornblende with rock chemistry and age are not as strong as for apatite, biotite, and sphene; igneous (?) epidote does not contain Cl and F in amounts detectable by electron microprobe analysis. The contents of Cl, F, and H 2 O+ in whole-rock samples decrease with increasing differentiation index and decreasing age. Data for a single pluton of variable composition mirror the results for a suite of different plutons and dikes. The data are satisfactorily although not exclusively explained by postulating that the melts each contained progressively less Cl, F, and H 2 O and that the hydrons minerals consumed most of the Cl, F, and H 2 O in the magmas. The data may also be explained by postulating that (1) the stocks evolved Cl-bearing water during their ascent and crystallization, or that (2) Cl and H 2 O were concentrated during differentiation of the stocks but the minerals failed to record their buildup. Both alternative explanations find problems with and require special conditions to satisfy field, chemical, and experimental data. If many of the special conditions are not met, a nearby batholithic parent to the stocks is not a favorable source of the mineralized fluids at Ray. Propylitic alteration of biotite results in Cl-poor chlorites and may have provided some Cl to hydrothermal fluids; biotite may have also supplied some F to propylitizing fluids through alteration.

Arizona↗

USGS1975

Perched silica minerals on mordenite fiber

Ellipsoidal quartz grains and spherulitic chalcedony are perched on mordenite fibers in geodes from Chihuahua, Mexico. Examination of samples of fibrous mordenite from six additional localities indicated that most mordenites have perched quartz crystals. A linear relationship exists between the Si:Al ratios and the refractive indices of the mordenites. The pH of the mineralizing solutions appears to be the primary factor controlling the presence of perched silica minerals (the lower the pH, the higher the Si:Al ratios and the lower the probability of precipitating quartz). Other factors that may affect the presence of lurched silica minerals are (1) the compactness of the mordenite fibers, (2) the morphology of the fibers, and (3) the concentration of Al, Ca, Na, and K in the mineralizing solutions.

Journal of Research of the U.S. Geological Survey↗

USGS2016

Coastal deposits of heavy mineral sands; Global significance and US resources

Ancient and modern coastal deposits of heavy mineral sands (HMS) are the principal source of several heavy industrial minerals, with mining and processing operations on every continent except Antarctica. For example, HMS deposits are the main source of titanium feedstock for the titanium dioxide (TiO 2 ) pigments industry, obtained from the minerals ilmenite (Fe 2 +TiO 3 ), rutile (TiO 2 ) and leucoxene (an alteration product of ilmenite). HMS deposits are also the principal source of zircon (ZrSiO 4 ), from which zirconium dioxide (ZrO 2 ) is obtained for uses mostly in refractory products. Sometimes monazite [(Ce,La,Nd,Th)PO 4 ] is recovered as a byproduct mineral, sought for its rare earth elements and thorium (Ault and others, 2016; Sengupta and Van Gosen, 2016; Van Gosen and Tulsidas, 2016).

Mining Engineering↗

USGS2014

Magmatism, metasomatism, tectonism, and mineralization in the Humboldt Range, Pershing County, Nevada

Introduction The Humboldt Range, Pershing County, Nevada, predominantly consists of Mesozoic igneous and sedimentary rocks that were modified several times by magmatism, metasomatism, and tectonism, and contain a variety of metallic (Ag, Au, Pb, Zn, Sb, W, Hg) and non-metallic (dumortierite, pinite, fluorite) mineral deposits (Knopf, 1924; Kerr and Jenney, 1935; Kerr, 1938; Cameron, 1939; Campbell, 1939; Kerr, 1940; Page et al., 1940; Johnson, 1977; Vikre, 1978; 1981; Crosby, 2012). Early Triassic Koipato Group volcanic rocks, which are widely exposed in the range, have been altered to quartz, muscovite (sericite), chlorite, pyrite, and other minerals during emplacement of Mesozoic intrusions and by crustal thickening. Most hydrothermal alteration of volcanic rocks and formation of mineral deposits involved externally derived water and other volatiles, although some volcanic strata were apparently altered by pore or dehydration water. Cospatial hydrothermal mineral assemblages and associations, produced by events widely spaced in time, are difficult to separate because of common mineralogy (quartz, sericite, and pyrite), partial to complete recrystallization, thermally compromised Ar geochronology, and lack of comprehensive investigations of volatile sources and deformational fabric. Distinguishing between metasomatic and metamorphic processes that affected rocks in the Humboldt Range is not straightforward.

Nevada↗

USGS2020

Precious and base metal mineralization within the lower stratigraphy of the Stillwater Complex: New targets defined and old targets revisited

Group Ten Metals is exploring for base and precious metals within the Stillwater Complex, a 2.7 Ga layered mafic/ultramafic intrusion, host to the world-class Sibanye platinum group element (PGE) mines. Group Ten controls approximately 25 kilometers of strike length of prospective mafic and ultramafic rocks in the western portion of the Complex. The property includes multiple target types and individual prospects. Stillwater Complex magmatic stratigraphy is divided into three major series based on the proportions of cumulus minerals—Basal, Ultramafic and Banded. Group Ten explores primarily within the lower third of the intrusion, from the Basal Series at the footwall contact, upwards into the Ultramafic Series which is divided into a lower Peridotite Zone and an upper Bronzitite Zone. Rocks of the Peridotite Zone are repetitive, laterally continuous and layered sequences of olivine, chromite and pyroxene cumulates. This model was developed in the eastern portion of the Complex. Mapping in the western portion of the Complex indicates that the Peridotite Zone is thinner than to the east and with cyclic units not as regularly developed. Group Ten has reviewed data from over 50 years of historical exploration in light of different commodity focus, land positions, analytical menus, and petrogenetic models to define a series of exploration targets. A six hole, 1,600 meter diamond drilling program targeting the Iron Mountain sector was completed in 2019; results are discussed in more detail below. At Iron Mountain the primary targets are Ni-Cu-PGE magmatic sulfides located within the Basal Series and lower Peridotite Zone, near the basal contact of the Complex. Important objectives included establishing the PGE tenor of sulfide mineralization drilled by AMAX in the 1970’s and penetrating basement rock rafts known to conceal mineralized (but not previously analyzed) ultramafic rocks beneath. Drilling also tested the PGE-enriched A-B chromitite package which rests stratigraphically above the previously tested zones. At Chrome Mountain, magmatic layering was disturbed or destroyed over large areas along a WNW axis that may be an artifact of early magma chamber deformation or result from much later, Laramide tectonism. Correlation of marker units, for example chromitite seams, are problematic in the disturbed area; these rocks are termed the Hybrid Unit. In addition, normal igneous stratigraphy appears to be intruded by discordant dunite masses, pyroxenite pegmatoids and magmatic breccias. This unusual assemblage of rock types is accompanied by significant and previously underappreciated PGE mineralization related to chromite schlieren and minor but persistent base metal sulfides.

Conference Paper↗

USGS2000

Alteration of reactive mineral surfaces by ground water

Two different investigations of shallow sandy aquifers inform our thinking about the role of reactive iron minerals in hydrogeological systems. Ground water in a number of settings has been described as having elevated concentrations of dissolved iron in anoxic portions of contaminant plumes (e.g. Baedecker et al., 1993; Lyngkilde and Christensen, 1992), and the coupling of microbial reduction of Fe(III) to the degradation of organic compounds links the study of the biogeochemistry of iron to our desire to understand processes influencing contaminated aquifers. Questions about the transport and fate of reactive constituents in ground water are linked to the study of iron through recognition of the importance of sorption processes on sesquioxide mineral surfaces common in sedimentary aquifers limiting the migration of metals, anions, and bacteria. We have been grappling with questions related to the stability of iron mineral phases in contaminated aquifers and the role of Fe(III)- bearing minerals and grain coatings as sorption substrates

Conference Paper↗

USGS2019

The US Geological Survey’s Earth Mapping Resources Initiative (Earth MRI)—Providing framework geologic, geophysical, and elevation data to the nation’s critical mineral-bearing regions

New detailed mapping of the geologic resources of the Nation has the potential to significantly close the gap in the essential data needed to fuel a modern era of economic development and technological innovation, while at the same time dramatically enhancing our understanding of the fundamental way geology impacts everyday life, from the domestic critical mineral resources that are necessary for modern technology and the economy, to domestic energy and water resources, geologic hazards, agriculture, and other pressing needs. The U.S. Geological Survey established the Earth Resources Mapping Initiative (Earth MRI) to address the shortfall in geologic, geophysical, and elevation data with sufficient detail to support evaluation of regions in the United States that have potential to host critical mineral resources. The new effort is a collaboration with the Association of American State Geologists, who are providing new detailed geologic maps and making available online archived data and information related to critical mineral resources. The geophysical and lidar surveys are being contracted through industry specialists to assure that high-quality data are available to the public. This article provides an overview of the Earth MRI effort with discussions on the initial geophysical surveys funded for areas that have known potential for rare earth element resources. Subsequent projects are being designed to address areas that may host other critical mineral resources.

Fast Times↗