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Airborne biogeophysical mapping of hidden mineral deposits

Airborne survey techniques have been developed to detect and map forest canopies affected by metal-induced stress. A high spectral resolution airborne spectroradiometer system, used over a known forest-covered copper soil anomaly, has revealed previously unknown spectral changes in the near-infrared chlorophyll absorption spectrum. The metal-induced spectral shifts have subsequently been reproduced in the laboratory at Columbia University. Waveform analysis techniques specifically designed for computer analysis of the high spectral resolution aircraft data filter out the very strong background noise introduced by variations in normal, unstressed vegetation canopy and by topographic effects. The wave-form method proves most effective in extracting the subtle spectral indicators of metal-induced stress. The analytic method is a unique frequency domain technique made possible by the high spectral resolution of the 500-channel spectroradiometer system. The biogeophysical technique is demonstrated by three mapping surveys of Cotter Basin, Montana, and Spirit Lake, Washington. This airborne mapping technique presents new application opportunities in large areas of the world where heavy forest cover has in the past made geologic and geophysical exploration tedious and expensive. The tree cover with widespreading and deeply penetrating root systems is turned to an advantage in the airborne biogeophysical technique by detecting metal-induced changes in the chlorophyll reflectance spectrum.

Montana↗

Derivation of S and Pb in phanerozoic intrusion-related metal deposits from neoproterozoic sedimentary pyrite, Great Basin, United States

The thick (≤8 km), regionally extensive section of Neoproterozoic siliciclastic strata (terrigenous detrital succession, TDS) in the central and eastern Great Basin contains sedimentary pyrite characterized by mostly high δ 34 S values (−11.6 to 40.8‰, >70% exceed 10‰; 51 analyses) derived from reduction of seawater sulfate, and by markedly radiogenic Pb isotopes ( 207 Pb/ 204 Pb >19.2; 15 analyses) acquired from clastic detritus eroded from Precambrian cratonal rocks to the east-southeast. In the overlying Paleozoic section, Pb-Zn-Cu-Ag-Au deposits associated with Jurassic, Cretaceous, and Tertiary granitic intrusions (intrusion-related metal deposits) contain galena and other sulfide minerals with S and Pb isotope compositions similar to those of TDS sedimentary pyrite, consistent with derivation of deposit S and Pb from TDS pyrite. Minor element abundances in TDS pyrite (e.g., Pb, Zn, Cu, Ag, and Au) compared to sedimentary and hydrothermal pyrite elsewhere are not noticeably elevated, implying that enrichment in source minerals is not a precondition for intrusion-related metal deposits. Three mechanisms for transferring components of TDS sedimentary pyrite to intrusion-related metal deposits are qualitatively evaluated. One mechanism involves (1) decomposition of TDS pyrite in thermal aureoles of intruding magmas, and (2) aqueous transport and precipitation in thermal or fluid mixing gradients of isotopically heavy S, radiogenic Pb, and possibly other sedimentary pyrite and detrital mineral components, as sulfide minerals in intrusion-related metal deposits. A second mechanism invokes mixing and S isotope exchange in thermal aureoles of Pb and S exsolved from magma and derived from decomposition of sedimentary pyrite. A third mechanism entails melting of TDS strata or assimilation of TDS strata by crustal or mantle magmas. TDS-derived or assimilated magmas ascend, decompress, and exsolve a mixture of TDS volatiles, including isotopically heavy S and radiogenic Pb from sedimentary pyrite, and volatiles acquired from deeper crustal or mantle sources. In the central and eastern Great Basin, the wide distribution and high density of small to mid-sized vein, replacement, and skarn intrusion-related metal deposits in lower Paleozoic rocks that contain TDS sedimentary pyrite S and Pb reflect (1) prolific Jurassic, Cretaceous, and Tertiary magmatism, (2) a regional, substrate reservoir of S and Pb in permeable and homogeneous siliciclastic strata, and (3) relatively small scale concentration of substrate and magmatic components. Large intrusion-related metal deposits in the central and eastern Great Basin acquired S and most Pb from thicker lithospheric sections.

Economic Geology↗

Organic matter diagenesis as the key to a unifying theory for the genesis of tabular uranium-vanadium deposits in the Morrison Formation, Colorado Plateau

Interstitial, epigenetic amorphous organic matter is intimately associated with uranium in the Grants uranium region on the southern part of the Colorado Plateau in northwestern New Mexico and is considered essential to genetic models for these deposits. In contrast, uranium minerals are intimately associated with authigenic vanadium chlorite and vanadium oxides in amorphous organic matter-poor ores of the Slick Rock and Henry Mountains mining districts on the northern part of the plateau, and therefore, in some genetic models amorphous organic matter is not considered crucial to the formation of these deposits. Differences in organic matter content can be explained by recognizing that amorphous organic matter-poor deposits have been subjected to more advanced stages of diagenesis than amorphous organic matter-rich deposits, during which organic compounds were broken down, solubilized, and removed during various diagenetic stages (e.g., sulfate reduction, methanogenesis, and organic acid production). Most diagenetic alterations (e.g., dissolution of framework grains and cements and precipitation of coarse-grained coffinite, vanadium clays, and vanadium oxides) characteristic of amorphous organic matter-poor deposits occurred when temperatures exceeded 80 degrees C--a temperature typical of the organic acid stage of diagenesis.Two factors combined to assure that a high percentage of the amorphous organic matter was removed from the Morrison Formation during diagenesis: the fact that the organic matter was humic (and therefore highly oxygenated), and that the juxtaposition of authigenic smectite and amorphous organic matter on grain rims facilitated clay mineral-organic catalysis reactions leading to the breakdown of large organic molecules into smaller, soluble molecules.Evidence that amorphous organic matter was involved in the genesis of organic matter-poor, as well as organic matter-rich, deposits includes the presence of leached iron-titanium oxides and strongly etched garnets (both attributed to leaching by organic acids), the gradation from organic matter-rich to organic matter-poor deposits in the Grants uranium region, the inverse correlation between the amount of amorphous organic matter and the intensity of diagenetic alteration, the ubiquitous occurrence of amorphous organic matter inclusions in coffinite, and the similarity in geometry of tabular uranium-vanadium ores and Holocene humate deposits. By recognizing that amorphous organic matter was crucial to the initial concentration of uranium (even in those deposits that presently contain little amorphous organic matter) and by recognizing the effects of the various stages of diagenesis on the ore, one genetic model may be applied to all of the sandstone-hosted, tabular-type uranium-vanadium deposits in the Morrison Formation on the Colorado Plateau.

Economic Geology↗

Metamorphism and gold mineralization in the Blue Ridge, southernmost Appalachians

Lode gold mineralization in the Blue Ridge of the southernmost Appalachians is hosted by metavolcanic rocks (e.g., Anna Howe mine, AL; Royal Vindicator mine, GA), metaplutonic rocks (e.g., Hog Mountain mine, AL), and metasedimentary rocks (e.g., Lowe, Tallapoosa, and Jones Vein mines, AL). Most gold occurs in synkinematic quartz + or - plagioclase + or - pyrite + or - pyrrhotite + or - chlorite veins localized along polydeformational faults that juxtapose rocks with significantly different peak metamorphic mineral assemblages.Mineralogy, chemistry, and O and H isotope studies suggest that the three types of host rocks have undergone differing amounts and types of alteration during mineralization. Limited wall-rock alteration in metavolcanic- and metasediment-hosted deposits, and relatively extensive wall-rock alteration in granitoid-hosted deposits, suggests that most deposits formed from fluids that were close to equilibrium with metavolcanic and metasedimentary rocks. Stable isotope compositions of the fluids calculated from vein minerals and vein selvages are consistent with a predominantly metasedimentary fluid source, but vary from deposit to deposit (-22 to -47ppm delta D, 4-5ppm, delta 18 O, and 5-7ppm delta 34 S at Anna Howe and Royal Vindicator; -48 to -50ppm delta D, 9-13ppm delta 18 O, and ca. 19ppm delta 34 S at Lowe and Jones Vein; and -22 to -23ppm delta D, 8-11ppm delta 18 O, 9-10ppm delta 34 S, and -6 delta 13 C at Hog Mountain). Silicate mineral thermobarometry of vein, vein selvage, and wall-rock mineral assemblages indicate that mineralization and regional metamorphism occured at greenschist to amphibolite facies (480 degrees + or - 75 degrees C at Anna Howe, 535 degrees + or - 50 degrees C at 6.4 + or - 1 kbars at Lowe, 530 degrees + or - 50 degrees C at 6.9 + or - 1 kbars at Tallapoosa, and 460 degrees + or - 50 degrees C at 5.5 + or - 1 kbars at Hog Mountain). Oxygen isotope fractionation between vein minerals and selvage minerals consistently records equilibration temperatures that are similar to or slightly lower than those estimated from silicate thermometry.Auriferous veins contain numerous fluid inclusions that were emplaced in several stages and can be subdivided into five compositional types based on salt and CO 2 concentrations. Fluid inclusion isochores for early formed inclusions from these veins intercept the pressure and temperature conditions estimated from silicate mineral thermobarometry and stable isotope thermometry, and are compatible with entrapment at those conditions. These fluids exhibit significant variation in salinity (X (sub NaCl equiv ) ) = 0.0-0.2) and CO 2 (X (sub CO 2 ) = 0.0-0.2), suggesting variation in fluid-wall-rock interaction that accompanied gold deposition during declining temperatures. Less abundant and later fluids within the veins are dominantly CO 2 .The association of gold mineralization with structurally controlled concordant and discordant quartz sulfide veins, and the temperatures and pressures of wall-rock alteration and regional metamorphism indicate that the present distribution of gold is a result of metamorphism during progressive D 2 -D 3 deformation. Isotopic data for alteration envelopes date this event as Alleghanian: 279 + or - 14 Ma (K-Ar whole rock) and 343 + or - 18 Ma (K-Ar biotite) at Lowe; and 315 + or - 18 Ma (Rb-Sr whole-rock isochron; 87 Sr/ 86 Sr i = 0.7061 + or - 0.0008) and 294 + or - 16 Ma (K-Ar whole-rock) at Hog Mountain. Available data are compatible with development of the lodes during early Alleghanian overthrusting of allochthons over sedimentary rocks of the autochthonous North American margin. The implication is that the fluids were derived from metasedimentary and/or metavolcanic formations in the lower parts of the crystalline thrust stack (or possibly from underlying autochthonous sedimentary formations), ascended along permeable fault zones, and were emplaced as veins into dilatent areas in and adjacent to the fault zones.

Economic Geology↗

Studies of fluid inclusions I: Low temperature application of a dual-purpose freezing and heating stage

The design and operation of a microscope freezing stage developed for use at magnifications up to 500X are described. It makes possible studies of low - temperature phase changes such as the freezing of a saline water phase, and hence an estimate of the total salt concentration, in fluid inclusions as small as 10 microns (10-6 milligram in weight). The crystal or polished mineral plate containing the inclusions is viewed while immersed in a thermostated heat exchange medium (acetone) circulating rapidly in order to minimize thermal gradients. The stage permits easy operation at temperatures down to -35° C, with electrical control to ±0.05° C, and to much lower temperatures with manual control. With substitution of silicone oil for acetone, the same stage can be used for heating experiments up to +250° C. Calibration points in the low range indicate the accuracy of freezing temperature determinations on optimum material to be better than ±0.1° C. The low relief of ice crystals in water solution places considerable importance on sample selection, preparation, and lighting. As a result of almost ubiquitous and drastic supercooling (meta-stability), -35° C is inadequate to freeze most inclusions . Holding at -78.5° C (acetone + solid CO 2 ) for thirty minutes is generally adequate, although a few samples require extended immersion in liquid nitrogen at -196° C to cause freezing of even a part of their inclusions . Such extensive supercooling is not possible with most surface waters owing to the presence of abundant extraneous solid nuclei for the crystallization of ice.

Economic Geology↗

Cruise Report; RV Moana Wave cruise M1-01-GM; the bathymetry and acoustic backscatter of the mid shelf to upper slope off Panama City, Florida, northeastern Gulf of Mexico; September 3, through October 12, 2001, Panama City, FL to Panama City, FL

A zone of deep-water reefs is thought to extend from the mid and outer shelf south of Mississippi and Alabama to at least the northwestern Florida shelf off Panama City, Florida (Figure 1, 67kb). The reefs off Mississippi and Alabama are found in water depths of 60 to 120 m (Ludwick and Walton, 1957; Gardner et al., in press) and were the focus of a multibeam echosounder (MBES) mapping survey by the U.S. Geological Survey (USGS) in 2000 (Gardner et al., 2000; in press). If this deep-water-reef trend does exist along the northwestern Florida shelf, then it is critical to determine the accurate geomorphology and type of the reefs that occur because of their importance as benthic habitats for fisheries. Precisely georeferenced high-resolution mapping of bathymetry is a fundamental first step in the study of areas suspected to be critical habitats. Morphology is thought to be critical to defining the distribution of dominant demersal plankton/planktivores communities. Fish faunas of shallow hermatypic reefs have been well studied, but those of deep ahermatypic reefs have been relatively ignored. The ecology of deep-water ahermatypic reefs is fundamentally different from hermatypic reefs because autochthonous intracellular symbiotic zooxanthellae (the carbon source for hermatypic corals) do not form the base of the trophic web in ahermatypic reefs. Instead, exogenous plankton, transported to the reef by currents, serves as the primary carbon source. Thus, one of the principle uses of the morphology data will be to identify whether any reefs found are hermatypic or ahermatypic in origin. Community structure and trophodynamics of demersal fishes of the outer continental of the northeastern Gulf of Mexico presently are the focus of a major USGS reseach project. A goal of the project is to answer questions concerning the relative roles played by morphology and surficial geology in controling biological differentiation. Deep-water reefs are important because they are fish havens, key spawning sites, and are critical early larval and juvenile habitats for economically important sport/food fishes. It is known that deep-water reefs function as a key source for re-population (via seasonal and ontogenetic migration) of heavily impacted inshore reefs. The deep-water reefs south of Mississippi and Alabama support a lush fauna of ahermatypic hard corals, soft corals, black corals, sessile crinoids and sponges, that together form a living habitat for a well-developed fish fauna. The fish fauna comprises typical Caribbean reef fishes and Carolinian shelf fishes, plus epipelagic fishes, and a few deep-sea fishes. The base of the megafaunal invertebrate food web is plankton, borne by essentially continuous semi-laminar currents generated by eddies, spawned off the Loop Current, that periodically travel across the shelf edge. A few, sidescan-sonar surveys have been made of areas locally identified as Destin Pinnacles, Steamboat Lumps Marine Reserve (Koenig et al., 2000; Scanlon, et al., 2000; 2001), Twin Ridges (Briere, et al., 2000; Scanlon, et al., 2000), and Madison-Swanson Marine Reserve (Koenig et al., 2000; Scanlon, et al., 2000; 2001). However, no quantitative and little qualitative information about the geomorphology and surficial geology can be gained from these data. Existing bathymetry along the northwestern Florida shelf suggests the existence of areas of possible isolated deep-water reefs. NOAA bathymetric maps NOS NH16-9 and NG16-12 show geomorphic expressions that hint of the presence of reefs in isolated areas rather than in a continuous zone. There has been no systematic, high-resolution bathymetry collected in this area, prior to this cruise. After the successful mapping of the deep-water reefs on the Mississippi and Alabama shelf (Gardner et al., 2000; in press), a partnership composed of the USGS, Minerals Management Service, and NOAA was formed to continue the deep-reef mapping to the northwest Florida mid shelf and upper slope. This cruise is the first fruit of that partnership.

Florida↗

Sinter-vein correlations at Buckskin Mountain, National district, Humboldt County, Nevada

At Buckskin Mountain (elev 2,650 m, 8,743 ft), Humboldt County, Nevada, a hydrothermal system, imposed on a middle Miocene volcanic sequence with contrasting permeabilities and tensile strengths, produced alteration assemblages controlled by elevation, from Hg-mineralized sinter to subjacent precious metal veins over a vertical distance exceeding 790 m. Sinter and epiclastic deposits, interpreted to be remnant paleosurface basinal strata enclosed by 16.6 to 16.1 Ma rhyolites, overlie older volcaniclastic basinal deposits and were part of a regional fluvial-lacustrine system developed among ca. 16 to 12 Ma basalt-rhyolite eruptive centers throughout the northern Great Basin. Because of contrasting erosional resistance among altered and unaltered rocks, Buckskin Mountain represents inverse topography with sinter and silicified epiclastic deposits at the summit. Sinter and veins, correlated by common elements, similar mineralogy, age constraints, textures, S isotope compositions, and fluid inclusion microthermometry, were deposited by sinter-vein fluid, the first of two sequential hydrothermal fluid regimes that evolved in response to magmatism, tectonism, hydrology, and topography. Thermal quenching of distally derived sinter-vein fluid in planar conduits caused deposition of banded quartz-silicate-selenide-sulfide veins ???270 to > 440 m below sinter at 16.1 Ma; vei??ns were initially enveloped by zoned selvages of proximal K-feldspar + K-mica + quartz + pyrite and distal illite + chlorite + calcite + pyrite. Mixing of sinter-vein fluid with local meteoric water in saturated basinal deposits caused deposition of silica, Hg-Se-S-Cl minerals, and precious metals in sinter and epiclastic deposits. Elevated ???Se/???S in sinter-vein fluid, and the relatively large stability fields of reduced aqueous selenide species in the temperature range of 250?? to <100??C, enabled (but was not the cause of) codeposition of selenide-sulfide minerals and common element associations in veins and sinter. Acid-sulfate fluid of the second fluid regime was derived from oxidation of H2S and other volatiles exsolved from sinter-vein fluid. Acid-sulfate fluid produced (1) a subhorizontal zone of partially leached basinal deposits and rhyolite from the paleosurface to a depth of ???60 m, and (2) laterally pervasive zones, ???100 to 200 m thick, of quartz + alunite ?? hematite and quartz + kaolinite + pyrite in volcaniclastic deposits immediately beneath partially leached rocks, but this fluid did not decompose selenide-sulfide-precious metal phases in sinter. Paragenetically late vein and wall-rock assemblages, including marcasite + pyrite, calcite, and kaolinite-replaced K minerals, record deeper transition of sinter-vein fluid into acid-sulfate fluid in vein conduits. This transition occurred as regional subsidence, manifested by the Goosey Lake depression immediately east of Buckskin Mountain, lowered the pieziometric surface at Buckskin Mountain, terminated sinter deposition, and caused boiling and/or degassing of sinter-vein fluid. The timing of subsidence is recorded by a decrease in alunite ages, from ca. 15.8 to 15.6 Ma, with depth below sinter. Lateral replacement of sinter and partially leached epiclastic deposits and rhyolite by opal-A marks the termination of the two hydrothermal regimes that lasted ???0.5 m.y. and followed rhyolitic volcanism of similar duration. Veins and sinter display textures that attest to plastic deformation, spalling, and gravitational settling, and indicate fluid-flow direction, velocity, and density stratification which, with conduit topology, may have influenced precious metal tenor in the veins. Components of sinter and veins were transported as colloids, formed in supersaturated sinter-vein fluid, that aggregated or coagulated as incompetent gelatinous layers in shallow pools and in underlying, near-vertical conduits in rhyolite and initially crystallized as opal and chalcedony. The low thermal conductivity of ho

Economic Geology↗

Geology and uranium-vanadium deposits of the slick rock district, San Miguel and Dolores counties, Colorado

Sedimentary rocks known in the Slick Rock district in southwestern Colorado range in age from Devonian (?) to Cretaceous, and aggregate about 13,000 feet in maximum thickness. Important uranium-vanadium production has come from deposits in the Salt Wash member of the Morrison formation of Late Jurassic age. The sedimentary rocks are gently folded in the Dolores and Glade anticlines and the Disappointment syncline, and are cut by the Dolores fault zone in the north part of the district and by the Glade fault zone in the south part of the district . Principal fracture sets are oriented approximately parallel to the major faults. Detrital hematite, magnetite, and ilmenite in rocks of the Morrison formation not affected by epigenetic alteration contain appreciable amounts of several of the elements found in the ore deposits . Epigenetic alteration processes have bleached large volumes of rock and largely destroyed these minerals. Such alteration is spatially associated with the Dolores fault zone. Most of the known ore deposits are in the north part of the Slick Rock district in a belt called the Dolores ore zone. The zone lies along the Dolores fault zone but is wider than the fault zone. All known deposits are associated with abundant carbonaceous plant material. Uranium-vanadium deposits in the district are chiefly tabular to lenticular and are roughly parallel to the sedimentary bedding. Some ore bodies, however, are narrow, elongate, and curve sharply across bedding; these bodies have been called "rolls" by the miners. Mineral zoning is evident in some roll bodies; carbonates, goethite (altered from pyrite), selenides, and sulfides are commonly found in concentric layers at the concave edge of rolls. This zoning, and the relationship of roll ore bodies to sedimentary structures and lithology, suggest that ore was deposited at an interface between two solutions, possibly cool connate water and a warmer ore solution. On a district scale, copper and lead are distinctly most abundant in the ore deposits within and immediately adjacent to the Dolores fault zone, and less abundant in deposits toward the edge of the zone. Uranium-vanadium deposits in the district occur only in sandstone that is considered to be epigenetically altered, and the most extensive epigenetic changes have occurred close to ore bodies. It is concluded that ground water, heated and set into circulation near the end of Cretaceous time by igneous intrusions in the La Sal and other centers on the Colorado Plateau, picked up elements from sedimentary rocks where they had been faulted and fractured, and deposited the elements at solution interfaces where accumulations of carbonaceous material provided favorable chemical conditions for precipitation.

Colorado, Utah↗

Environment of ore deposition at the Mex-Tex deposits, Hansonburg District, New Mexico, from studies of fluid inclusions

These deposits , in Pennsylvanian limestone and shale, contain barite, fluorite, low-silver galena with "J-type" lead, and quartz, and only minor amounts of other minerals. Mineralization occurs in veins, in blankets of bedded, rhythmically banded "coontail" ore , and in vuggy, coarsely crystalline open-space fillings in tectonic and solution channels in limestone adjacent to faults. Except for widespread silicification, the mineralization is very similar to that of the southern Illinois deposits . The main stages of hypogene mineralization are: 1) sphalerite, pyrite, galena and chalcopyrite; 2) five easily recognizable substages of fluorite with intermittent quartz and barite; and 3) late calcite.More than 500 primary and 2,500 pseudosecondary inclusions , mainly from fluorite, were studied on the freezing and heating microscope stages. Some primary inclusions contain organic matter. Gross supercooling indicates slow ore - fluid movement. Recognizable planes of pseudo-secondaries (each containing 20-200 inclusions ) yield data essentially identical with coeval primaries, but the few planes of presumed secondaries do not.The first three substages of fluorite formed from fluids that were essentially constant in temperature at 186°-205° C (assumed pressure correction +10° C), but increased in salinity from aproximately 10 up to 15 weight percent salts. Succeeding substages formed at gradually decreasing temperatures (to about 140° C) and increasing salinity (maximum 17%), with breaks marking several individual substages. A few inclusions in an early barite have anomalously low homogenization temperatures. Coarse selenite has primary inclusions full of fresh water and hence is presumed to be supergene.These data do not prove any given theory or origin for the fluids or the deposits , but they do place some limits on possible mechanisms of origin.

New Mexico↗

"Ribbon rock", an unusual beryllium-bearing tactite

The beryllium deposits at Iron Mountain, near the northern end of the Sierra Cuchillo in Sierra and Socorro Counties, New Mexico, are unusual products of contact metamorphism. They occur in irregular bodies of tactile formed by replacement of Paleozoic limestone, generally at or near contacts with small intrusive masses of rhyolite, aplite, and fine-grained granite. The metamorphism took place in mid-Tertiary time. Beryllium is present chiefly in the complex silicate minerals helvite and danalite, and is a minor constituent of the garnet grossularite, a boron-bearing idocrase, and chlorite. These minerals are known to occur in noteworthy concentrations in only one type of rock, a peculiar rhythmically layered variety of tactile to which the name "ribbon rock" is given. The structure of such tactite is very conspicuous, and appears in section as thin, finely crenulated bands of magnetite alternating with similar bands of silicate minerals and finely crystalline fluorite. Concentric banding about fluorite-rich pod-like masses is common. Bodies of "ribbon rock" range in size from inch-thick lenses to large masses amounting to thousands of tons; most appear to have been formed along contacts between re-crystallized limestone and massive magnetite-andradite tactite, chiefly by replacing fluids penetrating the limestone from fractures. The layered structure is interpreted as a diffusion effect.The formation of massive and "ribbon rock" tactites can be traced through a range of falling temperature from a stage characterized by deposition from iron-rich vapors to a stage in which hydrothermal solutions were dominant. Both vapors and liquids appear to have been acid. Reducing conditions undoubtedly existed during the latter part of the hydrothermal stage. The occurrence of beryllium in "ribbon rock," but not in typical massive tactite, may signify that its compounds in deposits at or near intrusive contacts are confined to rocks of hydrothermal origin. The occurrence of "ribbon rock" is suggested as a potentially useful clue for recognition of beryllium-bearing contact deposits elsewhere; at least two other occurrences of what apparently is "ribbon rock" have been described in the literature.

New Mexico↗

Constraints on the timing of Co-Cu ± Au mineralization in the Blackbird district, Idaho, using SHRIMP U-Pb ages of monazite and xenotime plus zircon ages of related Mesoproterozoic orthogneisses and metasedimentary rocks

The Blackbird district, east-central Idaho, contains the largest known Co reserves in the United States. The origin of strata-hosted Co-Cu ± Au mineralization at Blackbird has been a matter of controversy for decades. In order to differentiate among possible genetic models for the deposits, including various combinations of volcanic, sedimentary, magmatic, and metamorphic processes, we used U-Pb geochronology of xenotime, monazite, and zircon to establish time constraints for ore formation. New age data reported here were obtained using sensitive high resolution ion microprobe (SHRIMP) microanalysis of (1) detrital zircons from a sample of Mesoproterozoic siliciclastic metasedimentary country rock in the Blackbird district, (2) igneous zircons from Mesoproterozoic intrusions, and (3) xenotime and monazite from the Merle and Sunshine prospects at Blackbird. Detrital zircon from metasandstone of the biotite phyllite-schist unit has ages mostly in the range of 1900 to 1600 Ma, plus a few Neoarchean and Paleoproterozoic grains. Age data for the six youngest grains form a coherent group at 1409 ± 10 Ma, regarded as the maximum age of deposition of metasedimentary country rocks of the central structural domain. Igneous zircons from nine samples of megacrystic granite, granite augen gneiss, and granodiorite augen gneiss that crop out north and east of the Blackbird district yield ages between 1383 ± 4 and 1359 ± 7 Ma. Emplacement of the Big Deer Creek megacrystic granite (1377 ± 4 Ma), structurally juxtaposed with host rocks in the Late Cretaceous ca. 5 km north of Blackbird, may have been involved in initial deposition of rare earth elements (REE) minerals and, possibly, sulfides. In situ SHRIMP ages of xenotime and monazite in Co-rich samples from the Merle and Sunshine prospects, plus backscattered electron imagery and SHRIMP analyses of trace elements, indicate a complex sequence of Mesoproterozoic and Cretaceous events. On the basis of textural relationships observed in thin section, xeno-time and cobaltite formed during multiple episodes. The oldest age for xenotime (1370 ± 4 Ma), determined on oscillatory-zoned cores, may date the time of initial cobaltite formation, and provides a minimum age for the host metasedimentary rocks. Additional Proterozoic xenotime growth events occurred at 1315 to 1270 Ma and ca. 1050 Ma. Other xenotime grains and rims grew in conjunction with cobaltite during Cretaceous metamorphism. However, ages of these growth episodes cannot be precisely determined due to matrix effects on 206 Pb/ 238 U data for xenotime. Monazite, some of which encloses cobaltite, uniformly has Cretaceous ages that mainly are 110 ± 3 and 92 ± 5 Ma. These data indicate that xenotime, monazite, and cobaltite were extensively mobilized and precipitated during Middle to Late Cretaceous metamorphic events.

Idaho↗

A new model for tabular-type uranium deposits

Tabular-type uranium deposits occur as tabular, originally subhorizontal bodies entirely within reduced fluvial sandstones of Late Silurian age or younger. This paper proposes that belts of tabular-type uranium deposits formed in areas of mixed local and regional ground-water discharge shortly after deposition of the host sediments. The general characteristics of tabular-type uranium deposits, especially the most studied deposits, those in the Uravan mineral belt, Henry basin, and Grants uranium region, indicate that their essential feature was the formation at a density-stratified ground-water interface in areas of local and regional ground-water discharge. Reconstruction of the paleohydrogeology is the key to understanding the formation of these deposits. Gravity-driven ground water recharged in major highlands and discharged in lowlands at major concave changes in paleotopographic slope. Shallow local and deep regional ground-water systems were characterized by dilute and saline water, respectively. Typically, underlying marine rocks, especially evaporites, provided the solutes to the deep regional ground water. A density-stabilized interface existed at the ground-water divide between local and regional flow systems. Tabular-type uranium deposits formed where these divides or interfaces intersected pockets of reduction where organic matter accumulated. The precipitation of humate and uranium at an interface accounts for the tabular shape and the tendency of deposits to rise stratigraphically into the basin. Geologic ground-water controls that favor discharge, such as the pinch-out of major aquifers, are also favorable for uranium ore. The combination of topographic and geologic features that both cause discharge is most favorable for ore deposition.

Economic Geology↗

Environment of ore deposition in the Creede mining district, San Juan Mountains, Colorado; Part IV, source of fluids, from oxygen, hydrogen, and carbon isotope studies

The hydrogen isotopic composition of fluids responsible for formation of the near-surface silver-base metal vein deposits at Creede was measured by direct analysis of inclusion fluids in sphalerite, quartz, and rhodochrosite and was estimated from analyses of illite and chlorite. The oxygen isotopic composition was determined directly on inclusion fluids in sphalerite and was estimated from analyses of quartz, illite, rhodochrosite, siderite, and adularia. The carbon isotopic composition was estimated from analyses of rhodochrosite and siderite. The ranges in isotopic composition for water and CO 2 in the fluids associated with the formation of each of the minerals is given below (number of determinations given in parentheses):Mineral delta D (sub H 2 ) O ppm delta 18 O (sub H 2 ) O ppm delta 13 C (sub CO 2 ) ppmSphalerite -81 to -54 (4) -10.1 to -4.5 (4)Quartz -97 to -86 (4) -5.9 to 1.8 (18)Illite -62 to -50 (8) -1.6 to 1.2(7)Chlorite -64 to -55 (10) -2.2 to 0.8 (10)Adularia 4.2 (1)Rhodochrosite -82 to -78 (2) 4.2 to 9.4 (9) -5.7 to -4.2 (9)Siderite 4.9 to 9.9 (6) -6.9 to -2.7 (6)The delta D (sub H 2 ) O and delta 18 O (sub H 2 ) O values of fluids associated with the formation of sphalerite, quartz, illite/chlorite, and carbonate minerals differ substantially from one another, and these differences appear to have been maintained throughout the depositional history, regardless of the positions of the minerals in the paragenetic sequence.The data suggest that waters from three coexisting reservoirs fed the vein system alternately and episodically during vein formation, and apparently there was little mixing of the fluids from the different reservoirs. The hydrogen, oxygen, and carbon isotope data suggest that the carbonate waters were deep seated, probably dominantly magmatic, in origin. The sphalerite and illite/chlorite waters must have been dominantly meteoric in origin and substantially oxygen shifted by exchange with the volcanic country rocks. The quartz waters were also oxygen shifted meteoric waters but were some 40 per mil lower in deuterium content than the sphalerite and illite/chlorite waters.We propose that the quartz fluids entered the vein system from reservoirs beneath the mountainous areas to the north in the vicinity of the present Continental Divide, but that the sphalerite and illite/chlorite fluids entered the vein system from a topographically low area to the south along the structural moat of the Creede caldera. The difference in delta D between the two meteoric waters may reflect differences in altitude of the recharge areas for the two reservoirs or may be clue to isotopic evolution of the closed-basin lake and interstitial waters in the moat surrounding the Creede caldera.

Colorado↗

Structural framework, stratigraphy, and petroleum geology of the area of oil and gas lease Sale No. 49 on the U.S. Atlantic continental shelf and slope

On September 23, 1977, the U.S. Department of the Interior announced the tentative selection of 136 tracts for Sale No. 49 of oil and gas leases in the Baltimore Canyon Trough on the U.S. Atlantic Continental Shelf and Slope. This report summarizes the geology and petroleum potential of the area. The Baltimore Canyon Trough is an elongate, seaward-opening sedimentary basin filled by as much as 14 km of Mesozoic and Cenozoic sedimentary rocks. The basin first formed under the New Jersey shelf and gradually spread west and south as the area subsided after the rifting that formed the Atlantic basin. Rocks of the Triassic and Jurassic Systems together are more than 8 km thick in a depocenter areally restricted to the northern part of the trough. Basal Jurassic rocks are apparently nonmarine sedimentary rocks bedded with evaporite deposits. Direct evidence that some salt is in the basal Jurassic section comes from the Houston Oil and Minerals 676-1 well, which penetrated salt at a depth of about 3.8 km. During the Middle and Late Jurassic, more open marine conditions prevailed than in the Early Jurassic, and carbonate banks and reefs formed discontinuously along the seaward side of the shelf. Sand flats likely occupied the central part of the shelf, and these probably graded shoreward into nonmarine red beds that accumulated in a bordering coastal plain. Thick nonmarine sands and silty shales of Late Jurassic age were deposited in what is now the nearshore and midshelf area. These sedimentary rocks probably grade into thick marine carbonate rocks near the present shelf edge. During the Cretaceous, less sediment accumulated (about 4 km) than during the Jurassic, and most was deposited during Early Cretaceous time. The Cretaceous units show two main trends through time-a diminishing rate of sediment accumulation and an increase in marine character of sediments. During the Middle and Late Cretaceous, calcareous sand and mud filled the basin, buried the shelf-edge reefs and later spilled across the reefs into the oceanic basin as worldwide sea level reached a maximum. Cenozoic deposits are spread over the present shelf and adjacent Coastal Plain in overlapping sheets of marine and nonmarine sediment. The maximum thickness (1.5 km) is along the outer part of the present shelf. Major tectonic deformation in the Baltimore Canyon Trough area appears to have terminated near the end of the Early Cretaceous, when at least one large mafic intrusion (Great Stone dome) was emplaced. Upper Cretaceous sedimentary rocks are arched above older uplifted fault blocks near the shelf edge; this arching may be the result of draping due to differential compaction or, perhaps, minor movement of the fault blocks during Late Cretaceous time. The dominance of terrestrial over marine-derived organic matter in sediment samples from the COST No. B-2 well indicates that economic amounts of liquid petroleum hydrocarbons were probably not generated in the area but suggests a high potential for generation of wet or dry gas. Supporting evidence for the presence of natural-gas deposits on the slope comes from AMCOR 6021, the upper 305 m of which penetrated sediments that contained methane, ethane, and propane. Texaco, Inc., has announced that its 598-1 well yielded nearly 479,000 m s of natural gas per day from two zones during early testing. Further indication of possible gas deposits comes from analyzing the amplitude (bright spots) of seismic data. Geochemical studies of the COST No. B-2 well have shown that the shelf area of the Baltimore Canyon Trough has a relatively low geothermal gradient today and that it apparently has had a gradient as low or even lower throughout the Cretaceous to Holocene. A controversy exists concerning the maturity of the basal sediments penetrated by the COST No. B-2 well. Although significant amounts of gaseous hydrocarbons may have been generated, large amounts of liquid petroleum hydrocarbons probably hav

Circular↗

Platinum-group elements

The platinum-group elements (PGEs)—platinum, palladium, rhodium, ruthenium, iridium, and osmium—are metals that have similar physical and chemical properties and tend to occur together in nature. PGEs are indispensable to many industrial applications but are mined in only a few places. The availability and accessibility of PGEs could be disrupted by economic, environmental, political, and social events. The United States net import reliance as a percentage of apparent consumption is about 90 percent. PGEs have many industrial applications. They are used in catalytic converters to reduce carbon monoxide, hydrocarbon, and nitrous oxide emissions in automobile exhaust. The chemical industry requires platinum or platinum-rhodium alloys to manufacture nitric oxide, which is the raw material used to manufacture explosives, fertilizers, and nitric acid. In the petrochemical industry, platinum-supported catalysts are needed to refine crude oil and to produce aromatic compounds and high-octane gasoline. Alloys of PGEs are exceptionally hard and durable, making them the best known coating for industrial crucibles used in the manufacture of chemicals and synthetic materials. PGEs are used by the glass manufacturing industry in the production of fiberglass and flat-panel and liquid crystal displays. In the electronics industry, PGEs are used in computer hard disks, hybridized integrated circuits, and multilayer ceramic capacitors. Aside from their industrial applications, PGEs are used in such other fields as health, consumer goods, and finance. Platinum, for example, is used in medical implants, such as pacemakers, and PGEs are used in cancer-fighting drugs. Platinum alloys are an ideal choice for jewelry because of their white color, strength, and resistance to tarnish. Platinum, palladium, and rhodium in the form of coins and bars are also used as investment commodities, and various financial instruments based on the value of these PGEs are traded on major exchanges. PGEs are among the rarest metals; Earth’s upper crust contains only about 0.0005 part per million (ppm) platinum. Today, the average grade of PGEs in ores that are mined primarily for their PGE concentrations varies from 5 to 15 ppm, although the concentration of PGEs in hand-picked ore specimens may range from tens to hundreds of parts per million. More than 100 different minerals have one of the PGEs as an essential component. PGE minerals occur as native metals. They also occur as compounds with other transition metals (copper, iron, mercury, nickel, and silver), post-transition metals (bismuth, lead, and tin), metalloids (antimony, arsenic, and tellurium), and nonmetals (selenium and sulfur). From 1900 to 2011, approximately 14,200 metric tons of PGEs was produced, and roughly 95 percent of that production (13,500 metric tons) took place between 1960 and 2011. The breakdown of production by country shows that, since 1900, about 90 percent of the production came from South Africa and Russia. The secondary supply of platinum, palladium, and rhodium is obtained through the recycling of catalytic converters from end-of-life vehicles, jewelry, and electronic equipment. Recycled platinum, palladium, and rhodium provide a significant proportion of the world’s total supply; these secondary sources are sufficient to close the gap between world mine production and consumption. Exploration and mining companies report resources of about 104,000 metric tons of PGEs (including minor amounts of gold) in mineral deposits around the world that could be developed. For PGEs, almost all the reported production and identified resources are associated with deposits in three geologic features—the Bushveld Complex, which is a layered mafic-to-ultramafic intrusion in South Africa; the Great Dyke, which is a layered mafic-to-ultramafic intrusion in Zimbabwe; and sill-like intrusions associated with flood basalts in the Noril’sk-Talnakh area of Russia. The metallic forms of PGEs are generally considered to be inert. PGEs pose a risk to human health only in cases where individuals are occupationally exposed to synthetic PGE compounds, especially workers in precious-metal refineries. In the natural environment, background PGE concentrations are low in water, sediment, soil, and plants. Anthropogenic sources of PGEs in the environment include catalytic converters used in modern automobiles, platinum-based chemotherapy drugs, and smelter emissions. The abundance of sulfide minerals defines the environmental and geologic characteristics of PGE-enriched magmatic sulfide deposits; those deposits with the highest amount of sulfide minerals could have the highest environmental impact. Acid rock drainage from reef-type and contact-type deposits is unlikely because the ores and their host rocks contain low proportions of sulfide minerals. For some conduit-type orebodies with massive ores, mineral-processing techniques separate and produce concentrates of copper-, iron-, and nickel-bearing sulfide minerals; those with copper and nickel are processed to extract metal, but the iron-sulfide minerals, mainly pyrrhotite, are discarded as waste. This results in waste material with a high acid-generating potential. The most significant primary source of PGEs in the United States is a deposit in the Stillwater Complex, which is a layered igneous intrusion in Montana. Approximately 305 metric tons of platinum and palladium have been mined from the Stillwater Complex deposit since 1986. Exploration and development drilling indicate that another 2,200 metric tons are present. Mining has progressed to depths of 1,800 meters below the surface, but the bottom of the ore deposit has not been reached; geologic estimates suggest that another 1,000 to 6,200 metric tons of PGEs could be present at depth. In the future, PGEs may be mined from deposits found near the base of the Duluth Complex, which is a group of igneous intrusions in Minnesota.

Professional Paper↗

Copper in the United States, exclusive of Alaska and Hawaii

The copper districts in the United States (exclusive of Alaska and Hawaii) are shown on the accompanying map. In compiling the map, the estimated total quantity of copper present before mining was used to assign districts to size categories, and both production and reserves are included without distinction as to the status of exploitation. Four categories have been distinguished: deposits that contain 50+ to 1,000 tons; 1,000 to 50,000 tons; 50,000 to 1 million tons; and over 1 million tons of copper respectively. In many of the smaller deposits copper occurs with other metals, as gold, silver; lead, or zinc, that may be quantitatively and economically more important than the contained copper. Thus, for example, a deposit that contains large values in gold or zinc may contain only a small amount of copper and is shown on this map as a small copper deposit. Five principal morphologic types of deposits have been distinguished on the map by letter symbols. These are disseminated, replacement, vein, massive sulfide, and native copper deposits (see Explanation). They are not strictly genetic types, however, for the disseminated deposits, the massive sulfide deposits, and many of the vein deposits were formed largely or entirely by replacement processes. The symbols show either individual mines or the approximate centers of districts. Some of the more prominent districts are identified by name on the map, and all with over 1,000 tons of copper are numbered to correspond to the Locality Index. As mining district names do not always correspond to locality names, and a name established through common usage may not be the legal name of the mining district, several names are given in the index for some localities. The index is arranged alphabetically by States. Both published and unpublished data were used, and at least one reference is given for each locality if reports on it have been published.

Mineral Investigations Resource Map↗

U-Pb isotope systematics and age of uranium mineralization, Midnite mine, Washington.

Uranium ores at the Midnite mine, near Spokane, Washington, occur in phyllites and calcsilicates of the Proterozoic Togo Formation, near the margins of an anomalously uraniferous, porphyritic quartz monzonite of Late Cretaceous age. The present geometry of the ore zones is tabular, with the thickest zones above depressions in the pluton-country rock contact. Analyses of high-grade ores from the mine define a 207 Pb/ 204 Pb- 235 U/ 204 Pb isochron indicating an age of mineralization of 51.0 + or - 0.5 m.y. This age coincides with a time of regional volcanic activity (Sanpoil Volcanics), shallow intrusive activity, erosion, and faulting. U-Th-Pb isotopic ages of zircons from the porphyritic quartz monzonite in the mine indicate an age of about 75 m.y., hence the present orebodies were formed about 24 m.y. after its intrusion. The 51-m.y. time of mineralization probably represents a period of mobilization and redeposition of uranium by supergene ground waters, perhaps aided by mild heating and ground preparation and preserved by a capping of newly accumulated, impermeable volcanic rocks. It seems most likely that the initial concentration of uranium occurred about 75 m.y. ago, probably from relatively mild hydrothermal fluids in the contact-metamorphic aureole of the U-rich porphyritic quartz monzonite.Pitchblende, coffinitc, pyrite, marcasite, and hisingerite are the most common minerals in the uranium-bearing veinlets, with minor sphalerite and chalcopyrite. Coffinitc with associated marcasite is paragenetically later than pitchblende, though textural and isotopic evidence suggests no large difference in the times of pitchblende and colfinite formation.The U-Pb isotope systematics of total ores and of pitchblende-coffinite and pyrite-marcasite separates show that whereas open system behavior for U and Pb is essentially negligible for large (200-500 g) ore samples, Pb migration has occurred on a scale of 1 to 10 mm (out of pitchblende and coffinite and into pyrite and marcasite). Also, long-term continuous leakage of radioactive daughters of 238 U (probably 222 Rn) has occurred on scales of from approximately 100 mu m approximately 10 cm. The isotopic composition of unsupported radiogenic Pb in pyrite-marcasite seems to depend on the mineralogical microenvironment of the grains, so that the radiogenic Pb in pyrite-marcasite intimately intermixed with pitchblende-coffinite tends to be deficient in 206 Pb, and the radiogenic Pb in pyrite-marcasite in gangue tends to have excess 206 Pb. These systematics probably reflect differences between the average distances of Pb and 222 Rn diffusion since the formation of the ores.

Washington↗

Constraints from fluid inclusions on sulfide precipitation mechanisms and ore fluid migration in the Viburnum Trend lead district, Missouri

Measurements on fluid inclusions in hydrothermal dolomite cements place constraints on sulfide precipitation mechanisms and on the thermal-hydrologic processes which formed the Viburnum Trend Mississippi Valley-type lead district. Homogenization temperatures and freezing point depressions were determined for fluid inclusions in Bonneterre Dolomite-hosted dolomite cements in mine samples, as well as drill core from up to 13 km outside of the district. A well-defined cathodoluminescent zonation distinguishes dolomite growth zones in the Vi-burnurn Trend as older or younger than main-stage mineralization (octahedral galena) and facilitates correlation with other dolomites outside the Viburnum Trend.Homogenization temperatures and salinities in samples from mines are not systematically different from those of samples outside of the district. Medians of homogenization temperature distributions differ by not more than 25 degrees C, so that a temperature gradient, if present, should not have exceeded approximately 25 degrees C within the study area. These observations are interpreted to indicate that the Viburnum Trend was not strongly thermally anomalous with respect to surrounding country rock and that fluid flow occurred on a broad scale through not only the Lamotte Sandstone but through the overlying Cambrian carbonates as well.The absence of a significant, recognizable decrease in temperature either vertically within the section or east-west across the district, coupled with the minor amount of silica in the district, argues against cooling as a primary cause of sulfide precipitation. Fluids whose primary aquifer was the Lamotte Sandstone, predominantly a quartz arenite, should have been in equilibrium with quartz. Quartz in the Viburnum Trend occurs as a minor, drusy, vug-lining phase, but the district lacks the intense silicification found in other Mississippi Valley-type districts such as Tri-State (Oklahoma, Kansas, Missouri). Quartz solubility is strongly temperature dependent and, under equilibrium conditions, a decrease of 10 degrees C or more should have precipitated at least as many moles of silica as galena (assuming a galena solubility of between 1 and 10 ppm). Clearly this is not the case, as galena is far more abundant than quartz in the Viburnum Trend.Ice final-melting temperatures (T m ) in fluid inclusions generally range from -14 degrees to -27 degrees C for primary dolomite-hosted inclusions. Using these T m values and cation ratios for the inclusion fluids, absolute concentrations for the individual cations and chloride were calculated using the thermochemical model of Spencer et al. (1990). The corresponding high but variable salinities, 3.9 to 5.9 chloride molality, are evidence for the presence of more than one distinct fluid during mineralization.In a reduced sulfur mineralization model with Pb carried as chloride complexes, dilution is also a possible sulfide precipitation mechanism. The difference in Pb solubility (for an equal quantity of reduced sulfur) in the extremes of the chloride concentration range, 3.9 vs. 5.9 molal, reaches 1 ppm only for pH values below approximately 4.5. Accepting 1 ppm as a minimum metal concentration for a viable ore-forming fluid, dilution only appears capable of precipitating sulfides in a fluid with pH near the lower limit of values considered geologically reasonable or attainable.Dolomite cements hosting warm (approximately 105 degrees -125 degrees C) saline fluid inclusions are ubiquitous in the porous dolomitic facies of the Bonneterre Dolomite. Based on stratigraphic reconstructions, however, it is unlikely that the Bonneterre was buried deeper than 1.5 km. The distribution of warm inclusions beyond the Viburnum Trend district implies that fluid migration was regional in scale. Fluid inclusion temperatures inconsistent with typical basement heat-flow-controlled geothermal gradients (25 degrees -35 degrees C/km) may be explained by long-distance migration of warm, basin-derived brines. Elevated temperatures observed in fluid inclusions at shallow stratigraphic depths are consistent with a gravity flow hydrologic system characterized by rapid flow rates and the capacity for advective heat transport.

Economic Geology↗