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USGS1983

Iron disulfide minerals and the genesis of roll-type uranium deposits

FeS 2 minerals in host rocks for deposits that contain fossil vegetal (organic) matter differ in abundance, distribution, texture, and sulfur isotopic ratios from FeS 2 minerals in host rocks for deposits that do not contain fossil vegetal matter. In three South Texas deposits lacking such organic matter, preore FeS 2 is dominantly euhedral pyrite which formed in response to solutions emanating from these faults. Ore-stage FeS 2 is dominantly marcasite that occurs as overgrowths on preore pyrite. In three deposits (two in Wyoming and one in Texas) that contain organic matter, preore FeS 2 is also dominantly pyrite, but it occurs commonly as framboids and as replacements of plant fragments and is formed by bacterial sulfate reduction during early diagenesis and may be isotopically distinct from pyrite formed from fault-related fluids. Ore-stage FeS 2 in these deposits is primarily pyrite. Bacterial sulfate reduction provided sulfide for ore-stage pyrite in deposits which contain organic matter. Abiologic sulfur transformations tend to produce ore-stage marcasite in deposits that do not contain organic matter.

Economic Geology↗

USGS2013

Prospects for Ukrainian ferrous metals in the post-Soviet period

Two specialists on the mineral industries of the countries of the former USSR survey current problems confronting producers of ferrous metals in Ukraine and future prospects for domestic production and exports. A series of observations documenting the importance of ferrous metals production to Ukraine's economy is followed by sections describing investment plans and needs in the sector, and the role played by Ukraine within the iron and steel industry of the Soviet Union. The focus then turns to assessment of the current regional and global competitive position of Ukrainian producers for each of the major commodities of the sector-iron ore, manganese ore, ferroalloys, steel, and the products of the machine manufacturing and metal working industries. In conclusion, the paper discusses a potential regional industrial integration strategy analogous to that employed in the United States' Great Lakes/Midwest region, which possesses similar types of iron ore deposits and similar transport cost advantages and metallurgical and manufacturing industries.

Post-Soviet Geography and Economics↗

USGS1970

Economic geology of the Zipaquira quadrangle and adjoining area, Department of Cundinamarca, Colombia

At least four evaporite sequences are interbedded with Cretaceous strata in the Bogotga area of the Cordillera Oriental of Colombia. The easternmost and oldest evaporite interval is of probable Berriasian-Valanglnian age; the next oldest is of probable late Barremian-early Aptian age, and is followed by a possible late Aptian sequence. The westernmost and best known sequence is Turonian-early Coniacian in age, in the Sabana de Bogota. This youngest sequence contains the thickest known salt deposits and is probably the most widespread geographically. Three gypsum deposits of probable Barremian-Valanginian age are in the eastern part of the area under investigation. These deposits may have been leached from former salt accumulations. No other evaporites are exposed, but numerous brine springs are known, That the sources of these brines are neither deep not distant is suggested by the generally high concentrations, of the brines, the local presence of rute (leached salt residue), and the commonly significant amounts of H2S gas emitted at these springs. The rock salt exposed in three accessible mines commonly has a characteristic lamination caused by alternating layers of relatively pure halite and very argillaceous halite. Ubiquitously scattered throughout all salt deposits are small clasts of black, commonly pyritic, marly claystone. This lithology is also present as large claystone bodies conformably interbedded in the salt strata. Anhydrite is rare and is apparently more abundant at the Zipaquira mine that at the Nemocon and Upin mine. Paleontologic evidence in the Sabana de Bogota demonstrates that the salt-claystone series, hematite impregnated strata, and carbonaceous to locally coaly claystone are coeval. The salt-claystone facies may have been deposited in shallow evaporite pans that were separated within the overall evaporite interval by barriers on which the locally hematitic strata were deposited. The carbonaceous facies may also have formed in barrier areas or on the edges of the evaporite basins. Whether or not this facies relationship prevails in the older evaporite intervals is not known; meager evidence suggests that it does. Nonmetallic mineral resources other than the evaporite minerals are phosphate rock, limestone, kaolinite, and emeralds. Metallic mineral deposits present in the Zone include hematite at Pericos, La Caldera, Tibirita, Nueva Vizcaya, and Cerro de Montecristo; chalcopyrite at Cerro do Cobre and at Farallones de Medina; galena in several places along the Rio Farallones and Rio Gacheta; and spahlerite in the Junin district.

Open-File Report↗

USGS2010

Geochemical evolution of a high arsenic, alkaline pit-lake in the Mother Lode Gold District, California

The Harvard orebody at the Jamestown gold mine, located along the Melones fault zone in the southern Mother Lode gold district, California, was mined in an open-pit operation from 1987 to 1994. Dewatering during mining produced a hydrologic cone of depression; recovery toward the premining ground-water configuration produced a monomictic pit lake with alkaline Ca-Mg-HCO 3 -SO 4 –type pit water, concentrations of As up to 1,200 μ g/L, and total dissolved solids (TDS) up to 2,000 mg/L. In this study, pit-wall rocks were mapped and chemically analyzed to provide a context for evaluating observed variability in the composition of the pit-lake waters in relationship to seasonal weather patterns. An integrated hydrogeochemical model of pit-lake evolution based on observations of pit-lake volume, water composition (samples collected between 1998–2000, 2004), and processes occurring on pit walls was developed in three stages using the computer code PHREEQC. Stage 1 takes account of seasonally variable water fluxes from precipitation, evaporation, springs, and ground water, as well as lake stratification and mixing processes. Stage 2 adds CO 2 fluxes and wall-rock interactions, and stage 3 assesses the predictive capability of the model. Two major geologic units in fault contact comprise the pit walls. The hanging wall is composed of interlayered slate, metavolcanic and metavolcaniclastic rocks, and schists; the footwall rocks are chlorite-actinolite and talc-tremolite schists generated by metasomatism of greenschist-facies mafic and ultramafic igneous rocks. Alteration in the ore zone provides evidence for mineralizing fluids that introduced CO 2 , S, and K 2 O, and redistributed SiO 2 . Arsenian pyrite associated with the alteration weathers to produce goethite and jarosite on pit walls and in joints, as well as copiapite and hexahydrite efflorescences that accumulate on wall-rock faces during dry California summers. All of these pyrite weathering products incorporate arsenic at concentrations from <100 up to 1,200 ppm. In the pit lake, pH and TDS reach seasonal highs in the summer epilimnion; pH is lowest in the summer hypolimnion. Arsenic and bicarbonate covary in the hypolimnion, rising as stratification proceeds and declining during winter rains. The computational model suggests that water fluxes alone do not account for this seasonal variability. Loss of CO 2 to the atmosphere, interaction with pit walls including washoff of efflorescent salts during the first flush and seasonal rainfall, and arsenic sorption appear to contribute to the observed pit-lake characteristics.

California↗

USGS1955

Geochemistry and mineralogy of a uraniferous lignite [South Dakota]

Detailed studies have been carried out on a uraniferous lignite from the Mendenhall strip mine, Harding County, S. Dak. By means of heavy-liquid separations, a mineral-free concentrate of the lignite was obtained that contained 13.8 percent ash and 0.31 percent uranium in the ash. The minerals (gypsum 69 percent, jarosite 10 percent, quartz 2 percent, kaolinite and clay minerals 19 percent, and calcite trace) contain only 7 percent of the uranium in the original coal, indicating an association of the uranium with the organic components of the lignite.Batch extractions show that 88.5 percent of the uranium can be extracted from the lignite by two consecutive treatments with boiling 1 N hydrochloric acid. Continuous extraction with hot 6 N hydrochloric acid removes 98.6 percent of the uranium.Columns of coal were treated with water, 1 N hydrochloric acid, 6 N hydrochloric acid, and a solution of lanthanum nitrate. The experiment with lanthanum nitrate indicated that only 1.2 percent of the uranium in the coal is held by ion exchange. The elutriation experiments showed that the uranium is held in the coal as an organo-uranium compound or complex that is soluble at a pH of less than 2.18.A geochemical mechanism by which the uranium may have been introduced into and retained by the lignite is discussed.

South Dakota↗

USGS1981

A lithologic-tectonic framework for the metallogenic provinces of California

The lithologic-tectonic framework of California developed principally during Mesozoic time when various terranes of oceanic crust and island-arc crust were accreted to older sialic crust, resulting in westward growth of the continent. Emplacement of great batholithic masses of granitoid rocks cutting all these crustal types also took place during the Mesozoic period. The discrete tectonostratigraphic terranes that resulted from these events and subsequent Tertiary and Quaternary volcanic events are characterized by specific types of metallic mineral deposits or, in some terranes, by the virtual absence of deposits. Lead-silver-zinc replacement-type deposits are common in the Paleozoic carbonate terrane in the eastern part of the state and occur sporadically elsewhere in the miogeoclinal and cratonal terranes but are absent from the oceanic and island-arc terranes. The vast majority of contact metasomatic tungsten deposits, including all the large ones, are in pendants of miogeoclinal rocks in the Sierra Nevada batholith, but the important Atolia deposits reside in granitoid rocks that invade oceanic terrane. Molybdenum distribution closely follows that of tungsten. All the large contact metasomatic iron deposits in California are in craton and miogeoclinal terranes, but sparse small deposits of this type also occur in island-arc terranes of the northern Sierra Nevada and eastern Klamath Mountains. Lode gold deposits, although widely scattered, show a marked preference for oceanic and island-arc terranes that have been invaded by granitoid plutons. All the major deposits, including late Tertiary bonanza deposits such as Bodie, are in such terranes. It appears that magmatic processes were responsible for mobilizing and transporting the gold, but the metal was perhaps derived from the eugeosynclinal rocks, notably the mafic volcanics. Most mercury deposits are found in the Coast Ranges, where they commonly occur in silica-carbonate rock, an alteration product of serpentinite. The deposits appear to be spatially related to the Coast Range thrust, and the source of the mercury may have been sedimentary rocks of the underlying Franciscan assemblage. Epigenetic mineralization occurred at several different times during the Mesozoic, and again during Miocene and Pliocene time. The timing of mineralization events and the distribution of various deposit types indicate that no broad-scale zoning of epigenetic deposits exists around the Sierra Nevada batholith.Syngenetic deposits are represented mainly by massive sulfides, chert-associated manganese, and chromite. The massive sulfide deposits, with one exception, are restricted to island-arc terranes, and nearly all of these deposits are in silicic volcanic rocks. They are interpreted to be syngenetic with the enclosing rocks, although some redistribution of metals may have occurred after the original deposition. The deposits occur in volcanic sequences of at least five different ages ranging from Early Devonian to Late Jurassic or Early Cretaceous and, along with their enclosing rocks, were probably formed at some distance from their present sites. Chert-associated manganese deposits occur mainly in exotic blocks of oceanic crust in melange and probably formed in fairly deep ocean environments. Chromite is confined to ultramafic rock, much of which occupies suture zones separating various accreted terranes.

Economic Geology↗

USGS1997

Day one road log: Mid-Tertiary igneous rocks and mineral deposits in the central Wasatch Mountains, Utah

Today's field trip examines late Eocene and Oligocene granitoid intrusions, cogenetic volcanic rocks (Keetley Volcanics), and associated hydrothermally altered and mineralized rocks in the central Wasatch Mountains. Because of late Cenozoic tilting related to Basin and Range extension, a continuum of mid-Tertiary paleodepths is exposed that ranges from about 11 km on the west side of the Little Cottonwood stock to the actual paleosurface on the east side of the range (Fig. 1; John, 1989a). Consequently, we will see a wide variety of textures and styles of emplacement in the intrusive rocks, and a correspondingly wide variety of hydrothermal alteration types and mineral deposits (Lawton et al., 1980; John, 1989a). Mid-Tertiary igneous rocks in the central Wasatch Mountains consist of three phaneritic stocks exposed in the western and central parts of the range (Little Cottonwood, Alta, and Clayton Peak stocks); six porphyry to fine-grained phaneritic stocks exposed in the middle and eastern parts of the range, primarily in the Park City mining district (Flagstaff, Glencoe, Mayflower, Ontario, Pine Creek, and Valeo stocks); a subvolcanic porphyry complex (Park Premier stock) exposed near the Park Premier mine which is now partly covered by water filling the Jordanelle Reservoir; and coeval volcanic rocks (Keetley Volcanics), subvolcanic intrusions, and a volcanic neck (Indian Hollow plug) are exposed on the east side of the range (Figs. 2 and 3). The intrusive rocks range from coarse-grained, coarsely porphyritic on the west to fine-grained, porphyroaphanitic on the east (John, 1989a). They form a high-K, calc-alkaline series (Vogel

Utah↗

USGS2014

Mineral resource of the month: Iron and steel

Iron is one of the most abundant elements on Earth, but it does not occur in nature in a useful metallic form. Although ancient people may have recovered some iron from meteorites, it wasn’t until smelting was invented that iron metal could be derived from iron oxides. After the beginning of the Iron Age in about 1200 B.C., knowledge of iron- and steelmaking spread from the ancient Middle East through Greece to the Roman Empire, then to Europe and, in the early 17th century, to North America. The first successful furnace in North America began operating in 1646 in what is now Saugus, Mass. Introduction of the Bessemer converter in the mid-19th century made the modern steel age possible. Pig iron is a high-carbon alloy made by smelting iron ore in a blast furnace with carbonaceous material, typically coke, as a reducing agent. Limestone is added to the iron ore-coke charge as a fluxing agent to remove impurities. Steel is produced from pig iron by removing some of the carbon in a basic oxygen converter and adding several alloying elements, such as manganese, chromium, copper, nickel, titanium, molybdenum, tungsten and vanadium. Steel is also made by recycling ferrous scrap in an electric arc furnace. There are many grades of steel, but the three major types of steel are carbon, alloy and stainless. About 93 percent of the steel made in the United States is carbon steel, which contains a maximum 2 percent carbon. Applications are found in appliances, construction, shipbuilding, containers and packaging, as well as in the automotive, machinery and equipment industries. Alloy steel, about 5 percent of annual production, contains as much as 4 percent alloying elements. Special applications for alloy steel include use in machined parts and tool fabrication. Stainless steel, which accounts for about 2 percent of annual steel production, is formed by adding chromium and usually nickel to steel to make it highly corrosion-resistant. Since 2008, steelmaking capacity has greatly exceeded apparent steel consumption, primarily as a result of China’s rapid economic expansion and rapidly increasing capacity. This has resulted in an influx of steel products into the United States and other steelmaking countries that already have excess capacity. Demand by China’s steelmakers has also driven unprecedented increases in the prices of iron ore and metallurgical coal. In the short term, steelmaking capacity, globally and especially in China, is expected to continue to exceed steel consumption, with steel prices and production costs remaining stable.

Earth↗

USGS1956

Uranium deposits of the northern part of the Boulder Batholith, Montana

Uranium minerals and radioactivity anomalies occur in many silverlead veins and chalcedony veins and vein zones in the Boulder batholith of southwestern Montana. Pitchblende has been identified in a few silverlead veins. These silver-lead veins occupy shear zones along which there is no evidence of large-scale lateral displacement. The wall rock adjacent to the veins is intensely silicified and sericitized quartz monzonite and granodiorite. The veins have yielded substantial quantities of lead, silver, zinc, and gold. The silver-lead veins consist principally of galena, sphalerite, tetrahedrite, chalcopyrite, and pyrite in a gangue of light- to dark-gray quartz, altered rock, gouge, and subordinate chalcedony and carbonate minerals. No anomalous radioactivity nor uranium minerals have been found in similar veins in prebatholithic rocks of the area.Chalcedony veins and vein zones, some of which are uraniferous, are distinctly different from the silver-lead veins and, with a single exception, are known only in the batholith. The chalcedony vein zones consist of one or more discontinuous stringers or veins of chalcedony and microcrystalline quartz in silicified and sericitized quartz monzonite and granodiorite, and in less strongly altered alaskite. Only small amounts of silver ore have been produced from these chalcedony veins and vein zones. All of the veins are early Tertiary in age, but the silver-lead veins probably are older than the chalcedony veins. Uranium is closely associated with chalcedony and microcrystalline quartz in both types of veins. This association suggests that all of the uranium in the area is of the same age. If so, some of the silver-lead veins must have been re-opened during the period of chalcedony vein formation.

Montana↗

USGS1989

A reinterpretation of the δD H 2 O of inclusion fluids in contemporaneous quartz and sphalerite, Creede mining district, Colorodo: a generic problem for shallow orebodies?

Water extracted from fluid inclusions in quartz from shallow epithermal ore deposits often has a hydrogen isotope composition (δD) different from that of water extracted from inclusions in associated minerals. This difference is usually attributed to the involvement of primary fluids from multiple sources. Isotopic and homogenization and freezing temperature determinations on fluid inclusions from contemporaneous quartz and sphalerite from the epithermal, silver and base metal orebodies of the OH vein, Creede district, Colorado, suggest an alternative explanation. In near-surface deposits, differences between δD H 2 O of inclusion fluids in ore minerals and quartz may result, instead, from contamination during extraction of the fluids contained in primary inclusions by shallow ground water trapped in pseudosecondary inclusions in quartz. Quartz from the OH vein contains two principal petrographically distinct populations of fluid inclusions: primary and pseudosecondary. The primary inclusions have salinities ranging from 5 to 10 equiv wt percent NaCl, and the salinities of pseudosecondary inclusions cluster between 0 and 1 percent. Primary inclusions in quartz from one locality have a measured δD H 2 O value of -69 per mil, while pseudosecondary inclusions at the same locality have a δD H 2 O value of -102 per mil. Both salinity and isotopic values for primary inclusions in quartz are similar to those for primary inclusions in contemporaneous sphalerite. Homogenization temperatures for primary and pseudosecondary inclusions in quartz range from 191° to 280° C and from 199° to 278° C, respectively. The δD H 2 O value measured on fluid inclusions from bulk crystals ranges between -97 and -85 per mil and represents a mixture of fluids from both primary and pseudosecondary inclusions. We interpret the data to indicate that one or more episodes of abrupt incursion of cooler, overlying ground water into the ore zone caused thermal cracking of the quartz crystals during the time interval of mineralization. Subsequent healing of the fractures trapped heated, low-salinity ground water in pseudosecondary inclusions. The abrupt incursions of overlying ground water are speculated to have resulted from either collapse of a transient vapor-dominated region of the ore zone, or catastrophic venting of the system through hydrothermal eruption(s). The unusually high contrast between the salinities of the ore-depositing fluids and the ground water overlying the ore zone allowed recognition of this phenomenon at Creede. It is likely, however, that Creede is not unique. Similar phenomena may be common in shallow ore zones where rapid fluctuation of an interface between a deep, high-temperature thermal plume and an overlying, cooler ground water may be expected to occur. Careful study of the origins of fluid inclusions, particularly in quartz, is essential to characterize the primary ore fluids and to assess the role of ground water in the hydrology of shallow ore deposits.

Colorado↗

USGS1977

Data from geologic investigations in the Yemen Arab Republic during 1976

The results of semiquantitative spectrographic analyses for 31 elements in 126 specimens of rocks from the Yemen Arab Republic, collected mainly during February 1976 from the Precambrian area in the southeastern part of the country, provide background data for use in geochemical evaluation of areas potentially favorable for mineral deposits. Gold and thorium were undetected; the lower limits of determination are 10 parts per million (ppm) and 20 ppm, respectively. For the other elements, the abundances follow geochemical norms for crustal distribution: (1) Fe, Nb, and Zr in Holocene weathering products; (2) Ca and Sr in Pliocene limestone; (3) Mo in Pliocene(?) or Miocene(?) dikes; (4) Be, La, and Sn in Miocene(?) alkalic granite; (5) As, Be, and La in Tertiary and/or Cretaceous felsic tuff; (6) V in Tertiary and/or Cretaceous carbonaceous sedimentary rocks interbedded with volcanic rocks; (7) Be, La, Sn, and Zr in Tertiary and/or Cretaceous undivided volcanics; (8) Sn and W in Precambrian felsite and pegmatite; (9) Co, Cr, Ni, and Ti in Precambrian mafic rocks; (10) Mg and Sr in Precambrian marble and calcsilicate rocks; (11) Y in Precambrilan schist; (12) B and Sc dispersed in rocks of many ages; and (13) Ag, Ba, Bi, Cd, Cu, Mn, Pb, Sb, Sn, and Zn in a hydrothermal replacement deposit in Precambrian sediment. None of the rocks contained as much as 205 ppm equivalent uranium. The highest values for Ag, Cu, Pb, Zn, and Cd were obtained on a sample of hydrothermally altered siltstone not personally collected by the writers. It was said to have come from the Ma'rib area in the eastern part of the Yemen Arab Republic. The source must be studied, because this single sample is high-grade base-metal ore. Among the samples collected by the writers, the economically most significant are altered tuffs, ignimbrites, and felsites exposed between Jibal Hufash and Manakhah on the road from Hudaydah to San'a'. They are strongly anomalous for As and weakly anomalous, variously, for Hg, Mo, and Pb, which elements may constitute an epigenetic dispersion pattern from hidden sulfide deposits. Inasmuch as chalcopyrite and native copper have been reported in the vicinity of Jabal Haraz in the Manakhah area, the rocks of the Yemen Volcanics in this region should be explored for base-metal sulfide deposits. The first results of paleontologic examinations of fossils collected during 1975 and 1976 are presented, as are a list of Landsat images covering the Yemen Arab Republic, and a selected bibliography of reports on geology and the allied sciences relating to the Yemen Arab Republic.

Open-File Report↗

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↗

USGS2012

The physical hydrogeology of ore deposits

Hydrothermal ore deposits represent a convergence of fluid flow, thermal energy, and solute flux that is hydrogeologically unusual. From the hydrogeologic perspective, hydrothermal ore deposition represents a complex coupled-flow problem—sufficiently complex that physically rigorous description of the coupled thermal (T), hydraulic (H), mechanical (M), and chemical (C) processes (THMC modeling) continues to challenge our computational ability. Though research into these coupled behaviors has found only a limited subset to be quantitatively tractable, it has yielded valuable insights into the workings of hydrothermal systems in a wide range of geologic environments including sedimentary, metamorphic, and magmatic. Examples of these insights include the quantification of likely driving mechanisms, rates and paths of fluid flow, ore-mineral precipitation mechanisms, longevity of hydrothermal systems, mechanisms by which hydrothermal fluids acquire their temperature and composition, and the controlling influence of permeability and other rock properties on hydrothermal fluid behavior. In this communication we review some of the fundamental theory needed to characterize the physical hydrogeology of hydrothermal systems and discuss how this theory has been applied in studies of Mississippi Valley-type, tabular uranium, porphyry, epithermal, and mid-ocean ridge ore-forming systems. A key limitation in the computational state-of-the-art is the inability to describe fluid flow and transport fully in the many ore systems that show evidence of repeated shear or tensional failure with associated dynamic variations in permeability. However, we discuss global-scale compilations that suggest some numerical constraints on both mean and dynamically enhanced crustal permeability. Principles of physical hydrogeology can be powerful tools for investigating hydrothermal ore formation and are becoming increasingly accessible with ongoing advances in modeling software.

Economic Geology↗

USGS1998

Geodynamics of magmatic Cu-Ni-PGE sulfide deposits: New insights from the Re-Os isotope system

In this study, we reassess crustal contamination and sulfide ore-forming processes in some of the largest magmatic ore deposits, using published Re-Os isotope data and a modeling methodology that incorporates the R factor, defined as the effective mass of silicate magma with which a given mass of sulfide magma has equilibrated, in an Re-Os isotope mixing equation. We show that there is less disparity between conclusions based on Re-Os isotope data compared to other isotopic systems if the R factor is considered. Komatiite-associated Ni sulfide ore systems typically have high Os concentrations. low Re/Os ratios, and near-chondritic initial Os isotope compositions. For magmatic sulfide ores that are interpreted to have experienced relatively low R factors (<500), such as those at Kambalda, this severely limits the amount of wholesale crustal contamination as well as selective contamination of komatiitic magma by sedimentary sulfide components. The Re-Os geochemistry of these ores is most consistent with derivation from uncontaminated komatiites unless R factors are much higher (<2,000). Sulfide saturation in these ore systems may, therefore, have been achieved via changes in intensive parameters of the komatiite lavas cooling or decompression) or changes in compositional parameters transparent to the Re-Os isotope system (e.g., f O2 /f S2 /f H2O ). Basalt-gabbro-associated Cu-Ni sulfide ore systems at Duluth. Sudbury, and Stillwater are quite distinct from those at Kambalda by having comparatively low Os concentrations, high Re/Os ratios, and high initial Os isotope compositions. These chemical and isotopic characteristics are indicative of significant interactions between their parental basaltic magmas and old crust because there are no known mantle reservoirs with such extreme geochemical characteristics. Our modeling suggests that for Cu-Ni sulfide ores at Duluth, Sudbury, and Stillwater to maintain the observed high initial Os isotope compositions inherited from a crustal contaminant, R factors for these systems must have been low (<10,000), consistent with their low metal concentrations. Thus, we interpret this style of base metal sulfide mineralization to be derived from crustally contaminated but less dynamic magmatic systems that did not permit extensive equilibration of sulfide magma with silicate magma. For basalt-gabbro-associated Cu-Ni-PGE-rich sulfide ore systems that have Re-Os geochemical characteristics more similar to those associated with komatiites, R factors must have been high (>10,000 for Noril'sk-Talnakh and the J-M reef, Stillwater Complex). In these very dynamic magmatic ore systems, crustal contamination processes are more difficult to assess using Re-Os isotopes as the effects of contamination are masked by the R factor process in which sulfide magma equilibrates with extensive amounts of asthenospheric mantle-derived magma. Sulfide protore for these systems may, then, have been very radiogenic and of crustal origin prior to R factor processes that occurred during transport in feeder conduits and in upper crustal magma chambers. This study, therefore, highlights the need for caution when interpreting the Re-Os isotope geochemistry of sulfide ores from dynamic magmatic systems. The results of our reinvestigation of these giant ore deposits suggest that geodynamic processes associated with large magmatic systems, including major lithospheric pathways to the surface, changes in flow regime, coupled magma flow-through and magma mixing (providing enhanced R factors), may be critical to our understanding of the emplacement, localization, and quality of magmatic sulfide deposits. Thus, the timing and exact mechanism of sulfide saturation may be subordinate to dynamic magmatic processes in the localization of economic concentrations of magmatic sulfides.

Economic Geology↗

USGS2018

Quartz solubility in the H2O-NaCl system: A framework for understanding vein formation in porphyry copper deposits

Porphyry copper deposits consist of low-grade stockwork and disseminated sulfide zones that contain characteristic vein generations formed during the evolution of the magmatic-hydrothermal systems. The present contribution proposes an interpretive framework for the formation of porphyry veins that is based on quartz solubility calculations in the H 2 O-NaCl system at temperatures of 100° to 1,000°C and pressures of 1 to 2,000 bar. The model predicts that high-temperature (≳500°C) quartz in A veins of deep (≳4 km) porphyry deposits forms as a result of the cooling of ascending intermediate-density fluids at lithostatic conditions. In deposits of intermediate depths (~1.5–4 km), A vein quartz is mostly formed through cooling of ascending hydrothermal fluids under closed-system conditions or quasi-isobaric cooling under open-system conditions within the two-phase field of the H 2 O-NaCl system. In shallow (≲1.5 km) porphyry deposits, rapid decompression can also result in quartz precipitation, forming so-called banded veins. The high-temperature quartz in A veins is associated with potassic alteration. During continued cooling of the magmatic-hydrothermal system, quartz is formed at intermediate temperatures (≳375°–500°C). This quartz overprints earlier A veins and forms B veins. The fluid inclusion inventory of this quartz generation suggests formation at fluctuating pressure conditions, marking the lithostatic to hydrostatic transition, and the change of wall-rock behavior from ductile to brittle conditions. The quartz is precipitated because of cooling and decompression of the magmatic-hydrothermal fluids under K-feldspar-stable conditions. Textural evidence from many porphyry veins suggests that hypogene sulfide minerals present in A and B veins postdate the quartz, as contacts between quartz and sulfide minerals commonly show dissolution textures. Hypogene sulfide minerals in C veins form at conditions of retrograde quartz solubility, explaining why these veins contain little to no quartz. The quartz solubility calculations suggest that C vein formation occurs at temperatures of ~375° to 450°C from low-salinity, single-phase fluids escaping from the lithostatic to the hydrostatic environment. At the upper end of this temperature range, C veins are biotite stable. However, these veins are associated with chlorite, chlorite-K-feldspar, or chlorite-sericite alteration in most deposits. Late quartz is formed during continued cooling of the hydrothermal fluids at ≲375°C within the single-phase field of the H 2 O-NaCl system as quartz solubility under these conditions decreases with temperature. This process is responsible for the formation of quartz in D veins and later base metal-bearing E veins, which are associated with phyllic, advanced argillic, or argillic alteration.

Economic Geology↗

USGS2014

Aquifers of Arkansas: protection, management, and hydrologic and geochemical characteristics of groundwater resources in Arkansas

Sixteen aquifers in Arkansas that currently serve or have served as sources of water supply are described with respect to existing groundwater protection and management programs, geology, hydrologic characteristics, water use, water levels, deductive analysis, projections of hydrologic conditions, and water quality. State and Federal protection and management programs are described according to regulatory oversight, management strategies, and ambient groundwater-monitoring programs that currently (2013) are in place for assessing and protecting groundwater resources throughout the State. Physical attributes, groundwater geochemistry, and groundwater quality are described for each of the 16 aquifers of the State. Information in regard to the hydrology and geochemistry of each of the aquifers is summarized from about 550 historical and recent publications. Additionally, more than 8,000 sites with groundwater-quality data were obtained from the U.S. Geological Survey National Water Information System and the Arkansas Department of Environmental Quality databases and entered into a spatial database to investigate distribution and trends in chemical constituents for each of the aquifers. The 16 aquifers of the State were divided into two major physiographic regions of the State: the Coastal Plain Province (referred to as Coastal Plain) of eastern and southern Arkansas, which includes 11 of the 16 aquifers, and the Interior Highlands Division (referred to as Interior Highlands) of western Arkansas, which includes the remaining 5 aquifers. The 11 aquifers in the Coastal Plain consist of various geologic units that are Cenozoic in age and consist primarily of Cretaceous, Tertiary, and Quaternary sands, gravels, silts, and clays. Groundwater in the Coastal Plain represents one of the most valuable natural resources in the State, driving the economic engines of agriculture, while also supplying abundant water for commercial, industrial, and public-supply use. In terms of age from youngest to oldest, the aquifers of the Coastal Plain include Quaternary alluvial aquifers, including the Mississippi River Valley alluvial aquifer (the most important aquifer in Arkansas in terms of volume of use and economic benefits), the Jackson Group (a regional confining unit that served for decades as an important source of domestic supply), and the Cockfield, Sparta, Cane River, Carrizo, Wilcox, Nacatoch, Ozan, Tokio, and Trinity aquifers. The Mississippi River Valley alluvial aquifer accounts for approximately 94 percent of all groundwater used in the State, and the aquifer is used primarily for irrigation purposes. The Sparta aquifer is the second most important aquifer in terms of use, and the aquifer was used in the past dominantly as a source of public and industrial supply, although increasing irrigation use is occurring because of critically declining water levels in the Mississippi River Valley alluvial aquifer. Other aquifers of the Coastal Plain generally are used as important local sources of domestic, industrial, and public supply, in addition to other minor uses. Water quality generally is good for all aquifers of the Coastal Plain, except for elevated iron concentrations and localized areas of high salinity. The high salinity results from intrusion from underlying formations, evapotranspiration processes in areas of low recharge, and inadequate flushing in downgradient areas of residual salinity from deposition in marine environments. Trends in the spatial distribution of individual chemical constituents are related to position along the flow path for most aquifers of the Coastal Plain. These trends include elevated iron and nitrate concentrations with lower pH values and dissolved solids in groundwater from the outcrop areas, transitioning to lower iron and nitrate (related to changes in redox) and higher pH and dissolved solids (dominantly from the dissolution of carbonate minerals) in groundwater downgradient from outcrop areas. Groundwater generally trended from a calcium- to a sodium-bicarbonate water type with increasing cation exchange along the flow path. The Interior Highlands of western Arkansas has less reported groundwater use than other areas of the State, reflecting a combination of factors. These factors include prevalent and increasing use of surface water, less intensive agricultural uses, lower population and industry densities, lesser potential yield of the resource, and lack of detailed reporting. The overall low yields of aquifers of the Interior Highlands result in domestic supply as the dominant use, with minor industrial, public, and commercial-supply use. Where greater volumes are required for growth of population and industry, surface water is the greatest supplier of water needs in the Interior Highlands. The various aquifers of the Interior Highlands generally occur in shallow, fractured, well-indurated, structurally modified bedrock of this mountainous region of the State, as compared to the relatively flat-lying, unconsolidated sediments of the Coastal Plain. In terms of age from youngest to oldest, the aquifers of the Interior Highlands include: the Arkansas River Valley alluvial aquifer, the Ouachita Mountains aquifer, the Western Interior Plains confining system, the Springfield Plateau aquifer, and the Ozark aquifer. Spatial trends in groundwater geochemistry in the Interior Highlands differ greatly from trends noted for aquifers of the Coastal Plain. In the Coastal Plain, the prevalence of long regional flow paths results in regionally predictable and mappable geochemical changes along the flow paths. In the Interior Highlands, short, topographically controlled flow paths (from hilltops to valleys) within small watersheds represent the predominant groundwater-flow system. As such, dense data coverage from numerous wells would be required to effectively characterize these groundwater basins and define small-scale geochemical changes along any given flow path for aquifers of the Interior Highlands. Changes in geochemistry generally were related to rock type and residence time along individual flow paths. Dominant changes in geochemistry for the Ouachita Mountains aquifer and the Western Interior Plains confining system are attributed to rock/water interaction and changes in redox zonation along the flow path. In these areas, groundwater evolves along flow paths from a calcium- to a sodium-bicarbonate water type with increasing reducing conditions resulting in denitrification, elevated iron and manganese concentrations, and production of methane in the more geochemically evolved and strongest reducing conditions. In the Ozark and Springfield Plateau aquifers, rapid influx of surface-derived contaminants, especially nitrogen, coupled with few to no attenuation processes was attributed to the karst landscape developed on Mississippian- and Ordovician-age carbonate rocks of the Ozark Plateaus. Increasing nitrate concentrations are related to increasing agricultural land use, and areas of mature karst development result in higher nitrate concentrations than areas with less karst features.

Arkasas↗

USGS1981

A review of regional mineral resource assessment methods

Over 100 papers on regional mineral resource assessment of nonfuels are classified according to method(s) used and form(s) of product in order to help identify possible methods for future assessments. Types of products that have been used include: tons of metal; tons of rock and associated grade; gross value; potential; number of deposits; probability of one or more deposits; tons of rock, grade, and number of deposits by type; potential supply; and net value. Assessment methods considered are: time-rate, crustal abundance, cumulative tonnage versus grade, simple subjective, complex subjective, Bayesian, frequency, trend, geometric probability, multiple regression, discriminant analysis, modified component, multivariate logistic, cluster analysis or pattern recognition, and simulation.Selection of a method to be employed in an assessment should be based on: (1) appropriateness of the product to the problem, (2) limitations in resources, such as information or time available for the assessment, (3) the level of uncertainty and acceptability of biases in the assessment, and (4) the need for verification of results and acceptance of the method.

Economic Geology↗

USGS2012

Geologic setting, sedimentary architecture, and paragenesis of the Mesoproterozoic sediment-hosted Sheep Creek Cu-Co-Ag deposit, Helena embayment, Montana

The northern margin of the Helena Embayment contains extensive syngenetic to diagenetic massive pyrite horizons that extend over 25 km along the Volcano Valley-Buttress fault zone and extend up to 8 km basinward (south) within the Mesoproterozoic Newland Formation. The Sheep Creek Cu-Co deposit occurs within a structural block along a bend in the fault system, where replacement-style chalcopyrite mineralization is spatially associated mostly with the two stratigraphically lowest massive pyrite zones. These mineralized pyritic horizons are intercalated with debris flows derived from synsedimentary movement along the Volcano Valley-Buttress fault zone. Cominco American Inc. delineated a geologic resource of 4.5 Mt at 2.5% Cu and 0.1% Co in the upper sulfide zone and 4 Mt at 4% Cu within the lower sulfide zone. More recently, Tintina Resources Inc. has delineated an inferred resource of 8.48 Mt at 2.96% Cu, 0.12% Co, and 16.4 g/t Ag in the upper sulfide zone. The more intact upper sulfide zone displays significant thickness variations along strike thought to represent formation in at least three separate subbasins. The largest accumulation of mineralized sulfide in the upper zone occurs as an N-S–trending body that thickens southward from the generally E trending Volcano Valley Fault and probably occupies a paleograben controlled by normal faults in the hanging wall of the Volcano Valley Fault. Early microcrystalline to framboidal pyrite was accompanied by abundant and local barite deposition in the upper and lower sulfide zones, respectively. The sulfide bodies underwent intense (lower sulfide zone) to localized (upper sulfide zone) recrystallization and overprinting by coarser-grained pyrite and minor marcasite that is intergrown with and replaces dolomite. Silicification and paragenetically late chalcopyrite, along with minor tennantite in the upper sulfide zone, replaces fine-grained pyrite, barite, and carbonate. The restriction of chalcopyrite to inferred synsedimentary E- and northerly trending faults and absence of definitive zonation with respect to the Laramide Volcano Valley Fault in the lower sulfide zone suggest a diagenetic age related to basin development for the Sheep Creek Cu-Co-Ag deposit.

Montana↗