Geology Reports⌕ Search

SEARCH · Geology Reports

Results for “Rocks & Minerals”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,477 records · Page 82Linked to original sources

Sedimentary facies of iron-formation

The sedimentary iron -formations of Precambrian age in the Lake Superior region can be divided on the basis of the dominant original iron mineral into four principal facies : sulfide, carbonate, oxide, and silicate. As chemical sediments, these rocks reflect certain aspects of the chemistry of the depositional environments. The major control, at least for the sulfide, carbonate, and oxide types, probably was the oxidation potential. The evidence indicates that deposition took place in restricted basins, which were separated from the open sea by thresholds that inhibited free circulation and permitted development of abnormalities in oxidation potential and water composition. The sporadic distribution of metamorphism and of later oxidation permits description of the primary facies on the basis of unoxidized, essentially unmetamorphosed material. The sulfide facies is represented by black slates in which pyrite may make up as much as 40 percent of the rock. The free-carbon content of these rocks typically ranges from 5 to 15 percent, indicating that ultra-stagnant conditions prevailed during deposition. Locally, the pyritic rocks contain layers of iron -rich carbonate. The carbonate facies consists, in its purer form, of interbedded iron -rich carbonate and chert. It is a product of an environment in which oxygen concentration was sufficiently high to destroy most of the organic material but not high enough to permit formation of ferric compounds. The oxide facies is found as two principal types, one characterized by magnetite and the other by hematite. Both minerals appear to be of primary origin. The magnetite-banded rock is one of the dominant lithologies in the region; it consists typically of magnetite interlayered with chert, carbonate, or iron silicate, or combinations of the three. Its mineralogy and association suggest origin under weakly oxidizing to moderately reducing conditions, but the mode of precipitation of magnetite is not clearly understood. The hematite-banded rocks consist of finely crystalline hematite interlayered with chert or jasper. Oolitic structure is common. This facies doubtless accumulated in a strongly oxidizing, probably near-shore, environment similar to that in which younger hema-titic ironstones such as the Clinton oolite were deposited. The silicate facies contains one or more of the hydrous ferrous silicates (greenalite, minnesotaite, stilpnomelane, chlorite) as a major constituent. Granule structure, similar to that of glauconite, is typical of some varieties; others are nongranular and finely laminated. The most common association of the silicate rocks is with either carbonate- or magnetite-bearing rocks, which suggests that the optimum conditions for deposition ranged from slightly oxidizing to slightly reducing. The relationship between the iron -rich rocks and volcanism, stressed by many authors, is considered by the writer to be structural, not chemical: in the Lake Superior region both iron -deposition and volcanism are believed to be related to geosynclinal development during Huronian time. In Michigan, the lower Huronian rocks are iron -poor quartzite and dolomite-typical "stable-shelf" deposits; much of the upper Huronian consists of iron -poor graywacke and slate with associated volcanic rocks -a typical "geosynclinal" assemblage. Thus the iron -rich beds of the middle Huronian and lower part of the upper Huronian were deposited during a transitional stage in structural history. The major environmental requirement for deposition of iron - formation is the closed or restricted basin; this requirement coincides in time with what would be a normal stage in evolution of the geosyncline: namely, structural development of offshore buckles or swells that subsequently develop into island arcs characterized by volcanism.

Lake Superior↗

Isotopic analysis of radium geochemistry at discrete intervals in the Midwestern Cambrian-Ordovician aquifer system

Radium (Ra) is a geogenic radioactive contaminant that frequently occurs at elevated levels in the Midwestern Cambrian-Ordovician aquifer system (MCOAS). Geochemical indicators (e.g., redox conditions or total dissolved solids) can broadly characterize conditions associated with elevated Ra levels in groundwater, but do not consistently correlate to elevated Ra within specific stratigraphic horizons. A coupled geochemical and isotopic study of groundwater and aquifer solids for major and trace elements, Ra, and uranium (U) at discrete intervals in the MCOAS was used to elucidate processes that may be responsible for this disconnect, via analysis of groundwater as well as extracted and digested solid aquifer samples. We find that the potential for Ra mobilization varies by stratigraphic unit, as observed by whole-rock 226 Ra/ 238 U (dis)equilibrium. Overall, the examined aqueous geochemical characteristics (e.g., redox conditions, total dissolved solids) do not explain Ra concentrations within the system, suggesting that alternative factors, like solid-phase associations or the extent of alpha recoil damage, may be more important. A relation between aqueous 87 Sr/ 86 Sr and 226 Ra suggests that minerals with radiogenic 87 Sr/ 86 Sr are more likely to release 226 Ra to the aqueous system. Overall, the release of U and Ra due to water-rock interaction varies with discrete stratigraphy, depending on aqueous geochemistry and available mineral associations. Due to complex Ra-rock interactions and the heterogeneous geology of the MCOAS, aqueous geochemistry does not fully predict the mobilization and concentration of Ra in groundwater. As sources and sinks of Ra within the MCOAS vary across stratigraphy, knowledge of aqueous geochemistry, available solid-phase associations, and nuclide leachability all are important to consider for understanding elevated Ra occurrence in aquifer systems.

Wisconsin↗

U-Pb, Re-Os, and Ar/Ar geochronology of rare earth element (REE)-rich breccia pipes and associated host rocks from the Mesoproterozoic Pea Ridge Fe-REE-Au deposit, St. Francois Mountains, Missouri

Rare earth element (REE)-rich breccia pipes (600,000 t @ 12% rare earth oxides) are preserved along the margins of the 136-million metric ton (Mt) Pea Ridge magnetite-apatite deposit, within Mesoproterozoic (~1.47 Ga) volcanic-plutonic rocks of the St. Francois Mountains terrane in southeastern Missouri, United States. The breccia pipes cut the rhyolite-hosted magnetite deposit and contain clasts of nearly all local bedrock and mineralized lithologies. Grains of monazite and xenotime were extracted from breccia pipe samples for SHRIMP U-Pb geochronology; both minerals were also dated in one polished thin section. Monazite forms two morphologies: (1) matrix granular grains composed of numerous small (<50 μ m) crystallites intergrown with rare xenotime, thorite, apatite, and magnetite; and (2) coarse euhedral, glassy, bright-yellow grains similar to typical igneous or metamorphic monazite. Trace element abundances (including REE patterns) were determined on selected grains of monazite (both morphologies) and xenotime. Zircon grains from two samples of host rhyolite and two late felsic dikes collected underground at Pea Ridge were also dated. Additional geochronology done on breccia pipe minerals includes Re-Os on fine-grained molybdenite and 40 Ar/ 39 Ar on muscovite, biotite, and K-feldspar. Ages (±2 σ errors) obtained by SHRIMP U-Pb analysis are as follows: (1) zircon from the two host rhyolite samples have ages of 1473.6 ± 8.0 and 1472.7 ± 5.6 Ma; most zircon in late felsic dikes is interpreted as xenocrystic (age range ca. 1522–1455 Ma); a population of rare spongy zircon is likely of igneous origin and yields an age of 1441 ± 9 Ma; (2) pale-yellow granular monazite—1464.9 ± 3.3 Ma (no dated xenotime); (3) reddish matrix granular monazite—1462.0 ± 3.5 Ma and associated xenotime—1453 ± 11 Ma; (4) coarse glassy-yellow monazite—1464.8 ± 2.1, 1461.7 ± 3.7 Ma, with rims at 1447.2 ± 4.7 Ma; and (5) matrix monazite (in situ)—1464.1 ± 3.6 and 1454.6 ± 9.6 Ma, and matrix xenotime (in situ)—1468.0 ± 8.0 Ma. Two slightly older ages of cores are about 1478 Ma. The young age of rims on the coarse glassy monazite coincides with an Re-Os age of 1440.6 ± 9.2 Ma determined in this study for molybdenite intergrown with quartz and allanite, and with the age of monazite inclusions in apatite from the magnetite ore ( Neymark et al., 2016 ). A 40 Ar/ 39 Ar age of 1473 ± 1 Ma was obtained for muscovite from a breccia pipe sample. Geochronology and trace element geochemical data suggest that the granular matrix monazite and xenotime (in polygonal texture), and cores of coarse glassy monazite precipitated from hydrothermal fluids during breccia pipes formation at about 1465 Ma. The second episode of mineral growth at ca. 1443 Ma may be related to faulting and fluid flow that rebrecciated the pipes. The ca. 10-m.y. gap between the ages of host volcanic rocks and breccia pipe monazite and xenotime suggests that breccia pipe mineral formation cannot be related to the felsic magmatism represented by the rhyolitic volcanic rocks, and hence is linked to a different magmatic-hydrothermal system.

Missouri↗

Bokan Mountain peralkaline granitic complex, Alexander terrane (southeastern Alaska): evidence for Early Jurassic rifting prior to accretion with North America

The circular Bokan Mountain complex (BMC) on southern Prince of Wales Island, southernmost Alaska, is a Jurassic peralkaline granitic intrusion about 3 km in diameter that crosscuts igneous and metasedimentary rocks of the Alexander terrane. The BMC hosts significant rare metal (rare earth elements, Y, U, Th, Zr, and Nb) mineralization related to the last stage of BMC emplacement. U–Pb (zircon) and 40 Ar/ 39 Ar (amphibole and whole-rock) geochronology indicates the following sequence of intrusive activity: ( i ) a Paleozoic basement composed mainly of 469 ± 4 Ma granitic rocks; ( ii ) intrusion of the BMC at 177 ± 1 Ma followed by rapid cooling through ca. 550 °C at 176 ± 1 Ma that was synchronous with mineralization associated with vertical, WNW-trending pegmatites, felsic dikes, and aegirine–fluorite veins and late-stage, sinistral shear deformation; and ( iii ) intrusion of crosscutting lamprophyre dikes at >150 Ma and again at ca. 105 Ma. The peralkaline nature of the BMC and the WNW trend of associated dikes suggest intrusion during NE–SW rifting that was followed by NE–SW shortening during the waning stages of BMC emplacement. The 177 Ma BMC was synchronous with other magmatic centres in the Alexander terrane, such as (1) the Dora Bay peralkaline stock and (2) the bimodal Moffatt volcanic suite located ∼30 km north and ∼100 km SE of the BMC, respectively. This regional magmatism is interpreted to represent a regional extensional event that precedes deposition of the Late Jurassic – Cretaceous Gravina sequence that oversteps the Wrangellia and Alexander exotic accreted terranes and the Taku and Yukon–Tanana pericratonic terranes of the Canadian–Alaskan Cordillera.

Alaska↗

Prehnite- and pumpellyite-bearing mineral assemblages, west side of the Appalachian metamorphic belt, Pennsylvania to Newfoundland

Prehnite- and/or pumpellyite-bearing meta-igneous rocks are found on the west side of the Appalachian metamorphic belt (1) near Jonestown, south-eastern Pennsylvania; (2) on Rensselaer Plateau, eastern New York; (3) near Quebec City, Quebec; and (4) at Little Port, Humber Arm, western Newfoundland. The assemblages critical to determining the conditions of metamorphism are (1) chlorite-epidote-hematite-pumpellyite-prehnite; actinolite-chlorite-hematite-pumpellyite-stilpnomelane; (2) actinolite-chlorite-epidote-stilpnomelane; chlorite-epidote-pumpellyite-stilpnomelane; chlorite-epidote-hematite-pumpellyite; (3) chlorite-epidote-hematite-pumpellyite-stilpnomelane; chlorite-epidote-pumpellyite-prehnite; and (4) chlorite-epidote-prehnite; chlorite-prehnite-stilpnomelane; chlorite-epidote-pumpellyite-prehnite. One pumpellyite-bearing rock from western Newfoundland shows a later vein of analcime-calcite. All the assemblages also include quartz, sphene, calcite, K-mica, and albite. Analysis of the mineral assemblages by the Schreinemakers method for the phases actinolite-chlorite-epidote-hematite-prehnite-pumpellyite-stilpnomelane shows that the different localities can be assigned different metamorphic grades. Though the detailed results of the Schreinemakers analysis depend on the assumed source of ferric iron in epidote, the major conclusions are not affected. The thermodynamic role of calcite is more problematic, but it appears that CO 2 did not behave as a boundary-value component during metamorphism. If calcite is treated as an excess phase, the Schreinemakers bundle decomposes to a net in a multisystem. Plotted on such a net, the various localities again occupy different parts signifying different metamorphic grades. The occurrence of pumpellyite-bearing assemblages on the west flank of the northern Appalachian metamorphic belt might suggest that these assemblages, contrary to the ideas of Miyashiro and of others, do not indicate high-pressure and low-temperature type of metamorphism. These assemblages, however, are compatible with an alternative interpretation as remnants of a high-pressure, low-temperature Taconic metamorphic regime, whose imprint within most of the Appalachian metamorphic belt has been obliterated by later events. Such a reconstruction is compatible with the suggestion that this zone, lying near the margin of the early Paleozoic craton, was an active subduction zone during the Taconic orogeny.

Appalachian metamorphic belt↗

Antimony ore in the Fairbanks district, Alaska

Antimony-bearing ores in the Fairbanks district, Alaska, are found principally in two areas, the extremities of which are at points 10 miles west and 23 miles northeast of Fairbanks; and one of two minor areas lies along this same trend 30 miles farther to the northeast. These areas are probably only local manifestations of mineralization that affected a much broader area and formed antimony-bearing deposits in neighboring districts, the closest of which is 50 miles away. The ores were exposed largely as a result of lode gold mining, but at two periods in the past, high prices for antimony ore warranted an independent production and about 2500 tons of stibnite ore was shipped. The sulfide deposits occupy the same fractures along which a gold-quartz mineralization of greater economic importance occurred; and both are probably genetically related to igneous rocks which intrude the schistose country rock. The sulfide is in part contemporaneous with some late-stage quartz in which it occurs as disseminated crystals; and in part the latest filling in the mineralized zones where it forms kidney-shaped masses of essentially solid sulfide. One extremely long mass must have contained nearly 100 tons of ore, but the average of the larger kidneys is closer to several tons. Much of the ore is stibnite, with quartz as a minor impurity, and assays show the tenor to vary from 40 to 65 percent antimony. Sulphantimonites are less abundant but likewise occur as disseminated crystals and as kidney-shaped bodies. Antimony oxides appear on the weathered surface and along fractures within the sulfide ore. Deposits containing either stibnite or sulphantimonite are known at more than 50 localities, but only eighteen have produced ore and the bulk of this came from the mines. The geology of the deposit, and the nature, extent, and period of the workings are covered in the detailed descriptions of individual occurrences. Several geologic and economic factors, which greatly affect prospecting and mining for stibnite ore in the area, are outlined. The principal available ore and reserves are considered to be ores earlier mined but never shipped, ore minable from near-surface deposits, and ores recoverable as a by-product of future gold mining. The outlook for stibnite production in the district is very uncertain. Apparently the greater portion of stibnite ore has already been recovered and present operations will strip the two principal areas of the district. This conclusion is based on the scanty discoveries since the last war and the fact that the areas are so pock-marked with prospects that there is little likelihood that any other large near-surface bodies remain to be discovered. Future prospecting would essentially be limited to attempts to seek the continuation of lodes previously having high yields of stibnite.

Open-File Report↗

Magnesite and brucite in the United States, exclusive of Alaska and Hawaii

The important deposits of magnesite (MgCO 3 ) and brucite (MgO.H 2 O) in the United States (exclusive of Alaska and Hawaii) are shown on the accompanying map. Single deposits and groups of deposits are shown by geometric symbols according to four size categories based on estimated production plus reserves. These categories are: less than 10,000 tons, 10,000 to 100,000 tons, 100,000 to 1,000,000 tons, and more than 1,000,000 tons. Occurrences of mineralogic interest only are not shown. All map locations are numbered consecutively in each State and keyed to the locality index. The geographical coordinates in the locality index represent the centers of the geometric symbols. Thus, the same coordinates are assigned to all deposits covered by a group symbol. The map was compiled from published reports and data in the files of the United States Geological Survey. The names, geographic coordinates, and geologic types of deposits are given in the locality index. The principal published reports used in compiling the map are listed in the selected references. The main types of commercial deposits of magnesite in the United States are: (1) replacement bodies in limestone and dolomite; (2) replacements and veins in serpentine; and (3) sedimentary beds. Other magnesite deposits of varied origin and less common occurrence include beds associated with talc, chlorite, and mica schists; and veins and lenses in altered tuffs. Brucite is a relatively rare mineral of secondary origin which usually accompanies other magnesian minerals, particularly magnesite and hydromagnesite, and is associated with carbonate rocks and serpentine. Magnesite was first mined in California in 1886, and the State was the only domestic producer until the development of the Washington deposits began in 1916. In recent years, the main production of magnesite has been from Stevens County, Washington, and Nye County, Nevada. Production in California has been intermittent since 1945. Magnesite deposits in Texas were mined during and immediately after World War II. At present (1961) the only brucite deposits being worked are those at Gabbs, Nye County, Nevada. They have been mined almost continuously since 1935.

Mineral Investigations Resource Map↗

Element partitioning in magnetite under low-grade metamorphic conditions – A case study from the Proterozoic Belt Supergroup, USA

The distribution and partitioning of elements in igneous rocks is well established for various melt –(fluid) –solid pairs and provides important insights into the petrogenesis of these rocks. Studies of the partitioning behavior of elements under metamorphic conditions are scarce and commonly focus on high-grade metamorphic facies. Little is known about the partitioning behavior of elements under low-grade metamorphic conditions. Greenschist-facies metasedimentary rocks of the North American Belt Supergroup host magnetite that displays equilibrium features with co-existing mineral phases such as quartz and carbonate. Magnetite is an ideal target for geochemical investigations because it can incorporate a large number of cations and is sensitive to changes in temperature, oxygen fugacity, pressure, whole-rock composition, and cooling trends. Whole-rock major and trace element analyses have been undertaken on representative samples from Belt Supergroup metasedimentary rocks using X-ray luorescence. Electron microprobe and laser ablation ICP-MS were used to obtain major and trace element concentrations for magnetite hosted in these rocks. Stable-isotope geothermometry of magnetite–quartz and magnetite–carbonate pairs constrain metamorphic temperatures to ca. 390°C. Partition coefficients (D) for magnetite–matrix pairs presumably reflect equilibrium at these low-grade metamorphic conditions. Except for Mn and Ni, which show comparable partition coefficients, the calculated values are one to two orders of magnitude lower than those for igneous magnetite. Aluminum displays the lowest calculated partition coefficient with a value of 0.006 and Ni and Fe the highest values with 6.3 and 20.9, respectively. Of the elements that commonly occur in spinel-group minerals, two groups can be distinguished: (1) elements that preferentially partition into the host rock (D<1): Al, Mg, Pb, and Ti and (2) elements that show a preference to partition into magnetite (D>1): Zn, Mn, Cr, V, Ni, and Fe.

European Journal of Mineralogy↗

Central Colorado Assessment Project (CCAP)-Geochemical data for rock, sediment, soil, and concentrate sample media

This database was initiated, designed, and populated to collect and integrate geochemical data from central Colorado in order to facilitate geologic mapping, petrologic studies, mineral resource assessment, definition of geochemical baseline values and statistics, environmental impact assessment, and medical geology. The Microsoft Access database serves as a geochemical data warehouse in support of the Central Colorado Assessment Project (CCAP) and contains data tables describing historical and new quantitative and qualitative geochemical analyses determined by 70 analytical laboratory and field methods for 47,478 rock, sediment, soil, and heavy-mineral concentrate samples. Most samples were collected by U.S. Geological Survey (USGS) personnel and analyzed either in the analytical laboratories of the USGS or by contract with commercial analytical laboratories. These data represent analyses of samples collected as part of various USGS programs and projects. In addition, geochemical data from 7,470 sediment and soil samples collected and analyzed under the Atomic Energy Commission National Uranium Resource Evaluation (NURE) Hydrogeochemical and Stream Sediment Reconnaissance (HSSR) program (henceforth called NURE) have been included in this database. In addition to data from 2,377 samples collected and analyzed under CCAP, this dataset includes archived geochemical data originally entered into the in-house Rock Analysis Storage System (RASS) database (used by the USGS from the mid-1960s through the late 1980s) and the in-house PLUTO database (used by the USGS from the mid-1970s through the mid-1990s). All of these data are maintained in the Oracle-based National Geochemical Database (NGDB). Retrievals from the NGDB and from the NURE database were used to generate most of this dataset. In addition, USGS data that have been excluded previously from the NGDB because the data predate earliest USGS geochemical databases, or were once excluded for programmatic reasons, have been included in the CCAP Geochemical Database and are planned to be added to the NGDB.

Colorado↗

Porosity variability in limestone sequences

Porosity is the state of being porous, as measured by the percentage of bulk volume of a rock or soil that is occupied by space, whether isolated or connected. In hydrocarbon-bearing limestone settings, subsurface porous strata containing the oil or gas usually underlie non-porous caprock through which hydrocarbons cannot pass. In settings, subsurface freshwater aquifers beneath caprock can become contaminated by saltwater intrusion during periods of drought. Islands of the Florida Keys consist of two types of emergent 125-ka limestone, a highly porous fossil coral reef with large voids and a less porous oolite with small grains and interstices. Both limestones are capped by impervious laminated Holocene calcrete whose dimensions differ greatly (Figure 1a and b). Porosity variability in the limestones is thought to be the cause. The less permeable oolite retained rainfall moisture longer, allowing longer periods of calcrete buildup. Reddish and brownish layers in both illustrated calcrete samples represent periods of influx of non-carbonate minerals on African dust. The hiatus or gap in these rock records represents an interval of >115 kyr during which no marine or terrestrial deposition is recorded.

Book chapter↗

Geology of the Cooper Ridge NE Quadrangle, Sweetwater County, Wyoming

The Cooper Ridge NE 7?-minute quadrangle is 18 miles southeast of Rock Springs, Wyo., on the east flank of the Rock Springs uplift. Upper Cretaceous rocks composing the Rock Springs Formation, Ericson Sandstone, Almond Formation, Lewis Shale, Fox Hills Sandstone, and Lance Formation, Paleocene rocks composing the Fort Union Formation, and Eocene rocks composing the Wasatch Formation are exposed and dip 5?-8? southeast. Outcrops are unfaulted and generally homoclinal, but a minor cross-trending fold, the Jackknife Spring anticline, plunges southeastward and interrupts the northeast strike of beds. Older rocks in the subsurface are faulted and folded, especially near the Brady oil and gas field. Coal beds are present in the Almond, Lance, and Fort Union Formations. Coal resources are estimated to be more than 762 million short tons in 16 beds more than 2.5 feet thick, under less than 3,000 ft of overburden. Nearly 166 million tons are under less than 200 ft of overburden and are recoverable by strip mining. Unknown quantities of oil and gas are present in the Cretaceous Rock Springs, Blair, and Dakota Formations, Jurassic sandstone (Entrada Sandstone of drillers), Jurassic(?) and Triassic(?) Nugget Sandstone, Permian Park City Formation, and Pennsylvanian and Permian Weber Sandstone at the Brady field, part of which is in the southeast corner of the quadrangle, and in the Dakota Sandstone at the Prenalta Corp. Bluewater 33-32 well near the northern edge of the quadrangle. Other minerals include uranium in the Almond Formation and titanium in the Rock Springs Formation.

Professional Paper↗

Links between tectonics, magmatism, and mineralization in the formation of Late Cretaceous porphyry systems in the Yukon-Tanana upland, eastern Alaska, USA

Cretaceous-Paleocene porphyry Cu(±Mo±Au) occurrences are scattered throughout the Yukon-Tanana upland in eastern Alaska. Known occurrences in eastern Alaska are poorly characterized, despite a resurgence in exploration. Porphyry deposits in the upland are emplaced into structurally complex metamorphic rocks representing a variety of tectonic environments, resulting in diverse alteration and mineralization assemblages. New mapping, drill core logging, petrography, geochemistry, geochronology, and structural analysis allow improved characterization of the parameters of porphyry systems and identify key linkages to regional tectonic and magmatic events. New sericite 40 Ar/ 39 Ar and zircon U/Pb dates constrain porphyry systems to the Late Cretaceous-earliest Paleocene (ca. 71-63 Ma). Zircon Hf-isotope ratios and Ce and Eu concentrations indicate that Late Cretaceous-Paleocene intrusions emplaced into basement dominated by Triassic and Jurassic plutons are more isotopically juvenile, reflecting more oxidized conditions. In contrast, those emplaced into basement dominated by mid-Cretaceous plutons are more reduced crustal geochemical-affinity. Diversity in mineral assemblages in contrasting systems may reflect emplacement into crustal domains of varying compositions and oxidation states. Those formed within a domain containing more-oxidized Triassic and Jurassic plutons are molybdenite-rich and apparently lack gold. In contrast, systems formed within domains dominated by more reduced mid-Cretaceous plutons contain lower-sulfidation state mineral assemblages with reported gold.

Alaska, Yukon↗

Environmental effects of hydrothermal alteration and historical mining on water and sediment quality in Central Colorado

The U.S. Geological Survey conducted an environmental assessment of 198 catchments in a 54,000-km2 area of central Colorado, much of which is on Federal land. The Colorado Mineral Belt, a northeast-trending zone of historical base- and precious-metal mining, cuts diagonally across the study area. The investigation was intended to test the hypothesis that degraded water and sediment quality are restricted to catchments in which historical mining has occurred. Water, streambed sediment, and aquatic insects were collected from (1) catchments underlain by single lithogeochemical units, some of which were hydrothermally altered, that had not been prospected or mined; (2) catchments that contained evidence of prospecting, most of which contain hydrothermally altered rock, but no historical mining; and (3) catchments, all of which contain hydrothermally altered rock, where historical but now inactive mines occur. Geochemical data determined from catchments that did not contain hydrothermal alteration or historical mines met water quality criteria and sediment quality guidelines. Base-metal concentrations from these types of catchments showed small geochemical variations that reflect host lithology. Hydrothermal alteration and mineralization typically are associated with igneous rocks that have intruded older bedrock in a catchment. This alteration was regionally mapped and characterized primarily through the analysis of remote sensing data acquired by the ASTER satellite sensor. Base-metal concentrations among unaltered rock types showed small geochemical variations that reflect host lithology. Base-metal concentrations were elevated in sediment from catchments underlain by hydrothermally altered rock. Classification of catchments on the basis of mineral deposit types proved to be an efficient and accurate method for discriminating catchments that have degraded water and sediment quality. Only about 4.5 percent of the study area has been affected by historical mining, whereas a larger part of the study area is underlain by hydrothermally altered rock that has weathered to produce water and sediment with naturally elevated geochemical baselines.

Colorado↗

Geologic report and recommendations for the cobalt mission to Morocco sponsored by The Trade and Development Program of the International Development Cooperation Agency

A mission sponsored by the Trade and Development Program (TDP) of the International Development Cooperation Agency (IDCA) went to Morocco to evaluate the possibility of finding additional sources of cobalt in that country, as well as other types of mineralization. Information obtained during this trip shows Morocco to be a country for which much geologic information is available and in which there are many favorable target areas for future exploration. Work in the Bou Azzer district (Morocco's principal cobalt district) shows that much excellent geologic work has been done in searching for additional deposits. However, a number of useful approaches to locate cobalt have not been tried, and their use might be successful. The potential for undiscovered deposits in the Bou Azzer region seems very high. The cobalt mineralization in the Siroua uplift is different from that in the Bou Azzer district. However, geologic similarities between the two areas suggest that a genetic link may exist between the two types of mineralization. This further indicates that cobalt deposits of the Bou Azzer types might be present in the Siroua region. Examination of the Bleida copper mine shows it to be a well-exposed volcanic hosted stratabound copper deposit. Large unexplored areas containing similar rocks occur near this deposit and may contain as yet undiscovered copper mineralization.

Open-File Report↗

Analyzing legacy U.S. Geological Survey geochemical databases using GIS: applications for a national mineral resource assessment

This report emphasizes geographic information system analysis and the display of data stored in the legacy U.S. Geological Survey National Geochemical Database for use in mineral resource investigations. Geochemical analyses of soils, stream sediments, and rocks that are archived in the National Geochemical Database provide an extensive data source for investigating geochemical anomalies. A study area in the Egan Range of east-central Nevada was used to develop a geographic information system analysis methodology for two different geochemical datasets involving detailed (Bureau of Land Management Wilderness) and reconnaissance-scale (National Uranium Resource Evaluation) investigations. ArcGIS was used to analyze and thematically map geochemical information at point locations. Watershed-boundary datasets served as a geographic reference to relate potentially anomalous sample sites with hydrologic unit codes at varying scales. The National Hydrography Dataset was analyzed with Hydrography Event Management and ArcGIS Utility Network Analyst tools to delineate potential sediment-sample provenance along a stream network. These tools can be used to track potential upstream-sediment-contributing areas to a sample site. This methodology identifies geochemically anomalous sample sites, watersheds, and streams that could help focus mineral resource investigations in the field.

Egan Range↗

Metamorphism in the Adirondacks: II. The role of fluids

Quantitative estimates of metamorphic fluid speciation, stable isotopic analyses, and studies of fluid inclusions all document the local complexity of fluids in the deep crustal rocks exposed in the Adirondack Mountains, NY. Estimates of the activity of H 2 O in the granulite facies are substantially lower than in the amphibolite facies gneisses. The onset of low water activities in semi-pelitic gneisses generally correlates with migmatitic textures in the uppermost amphibolite facies, suggesting that partial melts absorbed H 2 O at the peak of metamorphism. In granulite facies marbles and calc-silicates, conditions varied from extremely undersaturated in H 2 O-CO 2 fluid to fluid saturated, and α H2O and α CO2 show sharp gradients within single outcrops. Low values of f O2 and f H2O , or of f CO2 , and f H2O indicate fluid-absent conditions for some orthogneisses and marbles, which are inferred to have been ‘dry’ rocks before and during granulite facies recrystallization. Wollastonite is preserved from early contact metamorphism and serves as an index mineral for fluid-absent conditions in granulites where α H2O is low. Values of f O2 range from near the hematite + magnetite buffer in metamorphosed iron formation to substantially below the quartz + magnetite + fayalite buffer in some orthogneisses. The anorthosite suite is more oxidized than some associated granitic gneisses. Halogens (F and Cl) substitute extensively for OH in micas and amphiboles, extending their stability, although F 2 , Cl 2 , HCl, and HF are minor components in any fluid. Oxybiotite-type exchanges involving O for OH are also important, extending the stability of biotite. Stable isotopic ratios of O and C demonstrate that premetamorphic whole-rock compositions are commonly preserved whereas mineral compositions generally reflect equilibration at the peak of metamorphism. The Marcy Anorthosite Massif was intruded as a high δ 18 O magma. The combination of mineral equilibria, stable isotope data, and fluid inclusions is used to identify and to distinguish among pre-orogenic contact metamorphic/hydrothermal events, peak metamorphic events, and retrograde/postmetamorphic events. Polymetamorphism is documented at skarn zones adjacent to anorthosite, where large volumes of hydrothermal fluid were channeled during early, shallow contact metamorphism and where conditions were fluid poor during subsequent regional metamorphism. Peak metamorphic events are inferred to have been caused primarily by magmatic processes of intrusion and anatexis. Partial melting has caused low values of α H2O in many rocks, but in other cases low values of α H2O are recorded in orthogneisses derived from H 2 O-poor magmas. Isotopic studies show that maximum fluid/rock ratios were <0·l and possibly 0·0 for infiltrating fluids at the peak of metamorphism in many localities. No evidence of pervasive, regional infiltration by a fluid at the peak of metamorphism has been substantiated in the Adirondacks. Fluid inclusions containing high-density CO 2 or CO 2 + H 2 O represent conditions from after the peak of metamorphism and document isobaric cooling, in agreement with estimates from garnet zoning. Fine-scale retrograde veins are common and are associated with high-density CO 2 -rich fluid inclusions.

New York↗

Mineral Resources of the Antelope Wilderness Study Area, Nye County, Nevada

At the request of the U.S. Bureau of land Management, 83,100 acres of the Antelope Wilderness Study Area (NV-4)60-231/241) was studied. In this report the studied area is called the 'wilderness study area', or simply the 'study area.' No identified mineral or energy resources occur within the study area. The southern part of the area has moderate mineral resource potential for undiscovered gold and silver, and the Woodruff Formation in the southern part of the area has high resource potential for undiscovered vanadium, zinc, selenium, molybdenum, and silver (fig. 1). This assessment is based on field geochemical studies in 1984 and 1985 by the U.S. Bureau of Mines and field geochemical studies and geologic mapping by the U.S. Geological Survey in 1984 and 1985. The remainder of the study area has low resource potential for undiscovered gold, silver, lead, zinc, manganese, tin, and molybdenum. The study area also has low resource potential for undiscovered oil and gas resources. The Antelope Wilderness Study Area is about midway between Tonopah and Eureka, Nev., in the northern Hot Creek Range and southern Antelope Range of central Nevada. It is accessible by unimproved dirt roads extending 20 mi (miles) north from U.S. Highway 6 and 40 mi south from U.S. Highway 50 (fig. 2). Most of the study area consists of rugged mountainous terrain having approximately 2,600 ft (feet) of relief. The mountain range is a block tilted gently to the east and bounded on both sides by normal faults that dip steeply to moderately west and have major displacements. Most of the study area is underlain by a thick sequence of Tertiary volcanic rocks that predominantly consist of silicic ash-flow tuff, the Windous Butte Formation. Paleozoic and lower Mesozoic (see geologic time chart in appendix) marine sediments occur along the southern margin of the study area, and lower Paleozoic rocks are exposed in the northeast corner. The areas of exposed Paleozoic-Mesozoic rocks along the southern margin of the study area have moderate mineral resource potential for gold and silver in sediment-hosted, disseminated, epithermal (low-temperature) gold-silver deposits (fig. 1). These rocks consist of folded and thrust-faulted, fine-grained clastic sediments and limestone and dolomite that locally have been brecciated and hydrothermally altered. The alteration (locally, strong silicification) and geochemical associations of these rocks indicate a favorable environment for such deposits. Exploration for disseminated gold deposits in the same geologic environment is currently being conducted just south of the study area. The remainder of the study area has low resource potential for epithermal gold and silver vein deposits in the Tertiary volcanic rocks. The Cenozoic sedimentary basins adjacent to the fault-bounded mountain block have moderate potential for petroleum resources; the study area itself has low potential for petroleum resources.

Bulletin↗

A topology of mineralization and its meaning for prospecting

Epigenetic mineral deposits are universal members of an orderly spatial and temporal arrangement of igneous rocks, endomorphic rocks, and hydrothermally altered rocks. The association and sequence of these rocks is invariant whereas the metric relations and configurations of the properties of these rocks are unlimited in variety. This characterization satisfies the doctrines of topology. Metric relations are statistical, and their modes are among the better guides to optimal areas for exploration. Metric configurations are graphically irregular and unpredictable mathematical surfaces like mountain topography. Each mineral edifice must be mapped to locate its mineral deposits. All measurements and observations are only positive or neutral for the occurrence of a mineral deposit. Effective prospecting is based on an increasing density of positive data with proximity to the mineral deposit. This means sampling for maximal numbers of positive data, pragmatically the highest ore-element assays at each site, by selecting rock showing maximal development of lode attributes.

Book chapter↗