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At least 1,387 records · Page 77Linked to original sources

The mineral resource potential of the Harrat Nawasif, sheet 21/42 C, Ranyah, sheet 21/42 D, and Jabal Dalfa, sheet 21/43 C quadrangles, Kingdom of Saudi Arabia

Areas with mineral resource potential in the Harrat Nawasif, Ranyah, and Jabal Dalfa quadrangles in the central Precambrian Shield of Saudi Arabia have been identified by reconnaissance rock geochemistry and inspection of ancient prospects. Locally anomalous areas in perthitic, alkalic granite terrane in the Ranyah quadrangle possibly contain niobium, zirconium, thorium, fluorite, rare-earth, tin, molybdenum, or copper mineralization. The reconnaissance rock geochemical survey in layered volcanic and volcaniclastic terrane in the Jabal Dalfa quadrangle identified a zinc anomaly in quartzite and a nickel-copper zone that is an extension of the Jabal Judayr prospect, where a low-grade, nickel-copper sulfide deposit is known. The Precambrian terrane in the Harrat Nawasif quadrangle has no known mineral resource potential.

Open-File Report↗

The triple argon isotope composition of groundwater on ten-thousand-year timescales

Understanding the age and movement of groundwater is important for predicting the vulnerability of wells to contamination, constraining flow models that inform sustainable groundwater management, and interpreting geochemical signals that reflect past climate. Due to both the ubiquity of groundwater with order ten-thousand-year residence times and its importance for climate reconstruction of the last glacial period, there is a strong need for improving geochemical dating tools on this timescale. Whereas 14 C of dissolved inorganic carbon and dissolved 4 He are common age tracers for Late Pleistocene groundwater, each is limited by systematic uncertainties related to aquifer composition and lithology, and the extent of water-rock interaction. In principle, radiogenic 40 Ar in groundwater acquired from decay of 40 K in aquifer minerals should be insensitive to some processes that impact 14 C and 4 He and thus represent a useful, complementary age tracer. In practice, however, detection of significant radiogenic 40 Ar signals in groundwater has been limited to a small number of studies of extremely old groundwater (>100 ka). Here we present the first high-precision (<1‰) measurements of triple Ar isotopes ( 40 Ar, 38 Ar, 36 Ar) in groundwater. We introduce a model that distinguishes radiogenic 40 Ar from atmospheric 40 Ar by using the non-radiogenic Ar isotopes ( 36 Ar, 38 Ar) to correct for mass-dependent fractionation. Using this model, we investigate variability in radiogenic 40 Ar excess (Δ 40 Ar) across 58 groundwater samples collected from 36 wells throughout California (USA). We find that Δ 40 Ar ranges from ~0‰ (the expected minimum value) to +4.2‰ across three study areas near Fresno, San Diego, and the western Mojave Desert. Based on measurements from a network of 23 scientific monitoring wells in San Diego, we find evidence for a strong dependence of Δ 40 Ar on aquifer lithology. We suggest that Δ 40 Ar is fundamentally controlled by the weathering of old K-bearing minerals and thus reflects both the degree of groundwater-rock interaction, which is related to groundwater age, and the integrated flow through different geological formations. Future studies of Late Pleistocene groundwater may benefit from high-precision triple Ar isotope measurements as a new tool to better interpret 14 C- and 4 He-based constraints on groundwater age and flow.

Chemical Geology↗

Electrical studies at the proposed Wahmonie and Calico Hills nuclear waste sites, Nevada Test Site, Nye County, Nevada

Two sites in the southwest quadrant of the Nevada Test Site (NTS) were investigated as potential repositories for high-level nuclear waste. These are designated the Wahmonie and Calico Hills sites. The emplacement medium at both sites was to be an inferred intrusive body at shallow depth; the inference of the presence of the body was based on aeromagnetic and regional gravity data. This report summarizes results of Schlumberger VES, induced polarization dipole-dipole traverses and magnetotelluric soundings made in the vicinity of the sites in order to characterize the geoelectric section. At the Wahmonie site VES work identified a low resistivity unit at depth surrounding the inferred intrusive body. The low resistivity unit is believed to be either the argillite (Mississippian Eleana Formation) or a thick unit of altered volcanic rock (Tertiary). Good electrical contrast is provided between the low resistivity unit and a large volume of intermediate resistivity rock correlative with the aeromagnetic and gravity data. The intermediate resistivity unit (100-200 ohm-m) is believed to be the intrusive body. The resistivity values are very low for a fresh, tight intrusive and suggest significant fracturing, alteration and possible mineralization have occurred within the upper kilometer of rock. Induced polarization data supports the VES work, identifies a major fault on the northwest side of the inferred intrusive and significant potential for disseminated mineralization within the body. The mineralization potential is particularly significant because as late as 1928, a strike of high grade silver-gold ore was made at the site. The shallow electrical data at Calico Hills revealed no large volume high resistivity body that could be associated with a tight intrusive mass in the upper kilometer of section. A drill hole UE 25A-3 sunk to 762 m (2500 ft) at the site revealed only units of the Eleana argillite thermally metamorphosed below 396 m (1300 ft) and in part highly magnetic. Subsequent work has shown that much if not all of the magnetic and gravity anomalies can be attributed to the Eleana Formation. The alteration and doming, however, still argue for an intrusive but at greater depth than originally thought. The electrical, VES, and IP data show a complex picture due to variations in structure and alteration within the Eleana and surrounding volcanic units. These data do not suggest the presence of an intrusive in the upper kilometer of section. The magnetotelluric data however gives clear evidence for a thick, resistive body in the earth's crust below the site. While the interpreted depth is very poorly constrained due to noise and structural problems, the top of the resistive body is on the order of 2.5 km deep. The IP data also identifies area of increased polarizability at Calico Hills, which may also have future economic mineralization.

Open-File Report↗

Acid-rock drainage at Skytop, Centre County, Pennsylvania, 2004

Recent construction for Interstate Highway 99 (I?99) exposed pyrite and associated Zn-Pb sulfide minerals beneath a >10-m thick gossan to oxidative weathering along a 40-60-m deep roadcut through a 270-m long section of the Ordovician Bald Eagle Formation at Skytop, near State College, Centre County, Pennsylvania. Nearby Zn-Pb deposits hosted in associated sandstone and limestone in Blair and Centre Counties were prospected in the past; however, these deposits generally were not viable as commercial mines. The pyritic sandstone from the roadcut was crushed and used locally as road base and fill for adjoining segments of I?99. Within months, acidic (pH<3), metal-laden seeps and runoff from the exposed cut and crushed sandstone raised concerns about surface- and ground-water contamination and prompted a halt in road construction and the beginning of costly remediation. Mineralized sandstones from the cut contain as much as 34 wt. % Fe, 28 wt. % S, 3.5 wt. % Zn, 1% wt. Pb, 88 ppm As, and 32 ppm Cd. A composite of <2 mm material sampled from the cut face contains 8.1 wt. % total sulfide S, 0.6 wt. % sulfate S, and is net acidic by acid-base accounting (net neutralization potential ?234 kg CaCO3/t). Primary sulfide minerals include pyrite, marcasite, sphalerite (2 to 12 wt. % Fe) and traces of chalcopyrite and galena. Pyrite occurs in mm- to cm-scale veinlets and disseminated grains in sandstone, as needles, and in a locally massive pyrite-cemented breccia along a fault. Inclusions (<10 ?m) of CdS and Ni-Co-As minerals in pyrite and minor amounts of Cd in sphalerite (0.1 wt. % or less) explain the primary source of trace metals in the rock and in associated secondary minerals and seepage. Wet/dry cycles associated with intermittent rainfall promoted oxidative weathering and dissolution of primary sulfides and their oxidation products. Resulting sulfate solutions evaporated during dry periods to form intermittent ?blooms? of soluble, yellow and white efflorescent sulfate salts (copiapite, melanterite, and halotrichite) on exposed rock and other surfaces. Salts coating the cut face incorporated Fe, Al, S, and minor Zn. They readily dissolved in deionized water in the laboratory to form solutions with pH <2.5, consistent with field observations. In addition to elevated dissolved Fe and sulfate concentrations (>1,000 mg/L), seep waters at the base of the cut contain >100 mg/L dissolved Zn and >1 mg/L As, Co, Cu, and Ni. Lead is relatively immobile (<10 ?g/L in seep waters). The salts sequester metals and acidity between rainfall events. Episodic salt dissolution then contributes pulses of contamination including acid to surface runoff and ground water. The Skytop experience highlights the need to understand dynamic interactions of mineralogy and hydrology in order to avoid potentially negative environmental impacts associated with excavation in sulfidic rocks.

Open-File Report↗

Quantitative approaches to characterizing natural chemical weathering rates

Silicate minerals, constituting more than 90% of the rocks exposed at the earth’s surface, are commonly formed under temperature and pressure conditions that make them inherently unstable in surficial environments. Undoubtedly, the most significant aspect of chemical weathering resulting from this instability is the formation of soils which makes life possible on the surface of the earth. Many soil macronutrients in this “critical zone” are directly related to the rate at which primary minerals weather (Huntington, 1995; Chadwick et al., 2003). Chemical weathering also creates economically significant ore deposits, such as those for Al and U (Samma, 1986; Misra, 2000), as well as potentially releasing high concentrations of toxic trace elements such as Se and As (Frankenberger and Benson, 1994). Silicate weathering is a significant buffer to acidification caused by atmospheric deposition (Driscoll et al., 1989) and from land use practices (Farley and Werritty, 1989). Atmospheric CO 2 levels have been primarily controlled by the balance between silicate weathering and the rate of volcanic inputs from the Earth’s interior, a relationship which may explain long-term climate stability (Ruddiman, 1997)

Book chapter↗

Magmatism and Epithermal Gold-Silver Deposits of the Southern Ancestral Cascade Arc, Western Nevada and Eastern California

Many epithermal gold-silver deposits are temporally and spatially associated with late Oligocene to Pliocene magmatism of the southern ancestral Cascade arc in western Nevada and eastern California. These deposits, which include both quartz-adularia (low- and intermediate-sulfidation; Comstock Lode, Tonopah, Bodie) and quartz-alunite (high-sulfidation; Goldfield, Paradise Peak) types, were major producers of gold and silver. Ancestral Cascade arc magmatism preceded that of the modern High Cascades arc and reflects subduction of the Farallon plate beneath North America. Ancestral arc magmatism began about 45 Ma, continued until about 3 Ma, and extended from near the Canada-United States border in Washington southward to about 250 km southeast of Reno, Nevada. The ancestral arc was split into northern and southern segments across an inferred tear in the subducting slab between Mount Shasta and Lassen Peak in northern California. The southern segment extends between 42&deg;N in northern California and 37&deg;N in western Nevada and was active from about 30 to 3 Ma. It is bounded on the east by the northeast edge of the Walker Lane. Ancestral arc volcanism represents an abrupt change in composition and style of magmatism relative to that in central Nevada. Large volume, caldera-forming, silicic ignimbrites associated with the 37 to 19 Ma ignimbrite flareup are dominant in central Nevada, whereas volcanic centers of the ancestral arc in western Nevada consist of andesitic stratovolcanoes and dacitic to rhyolitic lava domes that mostly formed between 25 and 4 Ma. Both ancestral arc and ignimbrite flareup magmatism resulted from rollback of the shallowly dipping slab that began about 45 Ma in northeast Nevada and migrated south-southwest with time. Most southern segment ancestral arc rocks have oxidized, high potassium, calc-alkaline compositions with silica contents ranging continuously from about 55 to 77 wt%. Most lavas are porphyritic and contain coarse plagioclase &plusmn; hornblende, biotite, and pyroxene phenocrysts. Seven epithermal gold-silver deposits with >1 Moz gold production, several large elemental sulfur deposits, and many large areas (10s to >100 km2) of hydrothermally altered rocks are present in the southern ancestral arc, especially south of latitude 40&deg;N. These deposits are principally hosted by intermediate to silicic lava dome complexes; only a few deposits are associated with mafic- to intermediate-composition stratovolcanoes. Large deposits are most abundant and well developed in volcanic fields whose evolution spanned millions of years. Most deposits are hundreds of thousands to several million years younger than their host rocks, although some quartz-alunite deposits are essentially coeval with their host rocks. Variable composition and thickness of crustal basement is the primary control on mineralization along the length of the southern ancestral arc; most deposits and large alteration zones are localized in basement rock terranes with a strong continental affinity, either along the edge of the North American craton (Goldfield, Tonopah) or in an accreted terrane with continental affinities (Walker Lake terrane; Aurora, Bodie, Comstock Lode, Paradise Peak). Epithermal deposits and quartz-alunite alteration zones are scarce to absent in the northern part of the ancestral arc above an accreted island arc (Black Rock terrane) or unknown basement rocks (Modoc Plateau). Walker Lane structures and areas that underwent large magnitude extension during the Late Cenozoic (areas with Oligocene-early Miocene volcanic rocks dipping >40&deg;) do not provide regional control on mineralization. Instead, these features may have served as local-scale conduits for mineralizing fluids.

Eastern California and Western Nevada↗

Tephroite in California manganese deposits

Recent studies of manganese deposits and mineral specimens in the Sierran belt of sedimentary rocks as well as in the Klamath Mountains to the north and in the Rand Mountains to the south, have shown the presence of tephroite , the orthosilicate of manganese (Mn2Si04), at numerous localities. Earlier studies of these deposits have shown that the original layered deposits of carbonate and hydrous silicates of manganese have been widely altered by metamorphism to spessartite (Mn3Al2-(SiO.),), rhodonite (MnSi03), and piedmontite (Ca2(Al,Mn"',Fe"')3-Si3Oi2(OH)). Recent work shows that layered manganese oxides also were present in the original sedimentary rocks. It shows also, that tephroite has formed widely in the original assemblage of carbonate, silicate, and oxide of manganese ; in several localities, a little alleghanyite (2Mn2-S1O4 - Mn(OH,F)2) has been formed. Rhodonite, spessartite, and piedmontite uniformly follow the tephroite ; in places, bementite and neotocite are present. In one deposit a little pyroxmangite ( (Mn,Fe,Ca)Si03) has been noted and in another, some crystals that are probably pyrophanite (MnTi03), not yet recorded in the United States. By contrast, the restudy of large collections of material from deposits in sedimentary rocks of the Franciscan formation in the Coast Ranges indicates the tephroite is very uncommon; it has been recognized with assurance at only one locality-Alum Rock Park, Santa Clara County. In the Coast Ranges, rhodonite and spessartite, the high manganese garnet, are very uncommon. The assemblages of manganese silicates indicate that the layered deposits of manganese minerals in the Sierra belt have been metamorphosed to a higher degree than those of the Coast Ranges. This review also shows the presence of axinite, the boro-silicate of aluminum, calcium, and manganese , in three deposits .

California↗

Geology of the Copper King Mine area, Prairie Divide, Larimer County, Colorado (Part 1)

The Copper King mine, in Larimer County, Colo., in the northern part of the Front Range of Colorado, was operated for a short time prior to World War II for copper and zino, but since 1949, when pitchblende was discovered on the mine dump, it has been worked for uranium. The bedrock in the mine area consists predominantly of pre-Cambrian (Silver Plums) granite with minor migmatite and metasediments--biotite-quartz-plagioclase gneiss, biotite schist, quartzite, amphibolite, amphibole skarn, and biotite skols. The metasediments occur as inclusions that trend northeast in the granite. This trend is essentially parallel to the prevailing foliation in the granite. At places the metasediments are crosscut sharply by the granite to form angular, partly discordant, steep-walled bodies in the granite. Faults, confined to a narrow zone that extends through the mine, cut both the pre-Cambrian rocks and the contained sulfide deposits. The Copper King fault, a breccia zone, contains a deposit of pitchblende; the other faults are believed to be later than the ore. The two types of mineral deposits--massive sulfide and pitchblende deposits--in the mine area, are of widely different mineralogy, age, and origin. The massive sulfide deposits are small and consist of pyrite, sphalerite, chalcopyrite, pyrrhotite, and in places magnetite in amphibole skarn, mice skols, and quartzite. The deposit at the Copper King mine has yielded small quantities of high-grade sphalerite ore. The massive sulfides are pyrometasomatic deposits of pre-Cambrian age. The pitchblende at the Copper King mine is principally in the Copper King vein, a tight, hard breccia zone that cuts through both granite and the massive sulfide deposit. A small part of the pitchblende is in small fractures near the vein and in boxwork pyrite adjacent to the vein; the post-ore faults, close to their intersection with the Copper King vein, contain some radioactive material, but elsewhere, so far as is known, they are barren. The pitchblende in the deposit forms a steeply plunging ore shoot that has a horizontal length of more than 50 feet and a vertical height of about 85 feet. The thickness of the ore shoot averages about 2 feet, but it ranges from a feather edge to about 4 feet. The hard pitch-blende is intimately intergrown with siderite; other gangue minerals include pyrite, quartz, and finely comminuted fragments of the wall rocks. The vein was repeatedly reopened during mineral deposition as shown by several stages of brecciation and recommended by the vein matter. The pitchblende deposit probably formed at intermediate temperatures and depths and, according to the Pb/U ratio, is about 60 million years old--an early Tertiary age.

Colorado↗

The Iron Hill (Powderhorn) carbonatite complex, Gunnison County, Colorado — A potential source of several uncommon mineral resources

A similar version of this slide show was presented on three occasions during 2008: two times to local chapters of the Society for Mining, Metallurgy, and Exploration (SME), as part of SME's Henry Krumb lecture series, and the third time at the Northwest Mining Association's 114th Annual Meeting, held December 1-5, 2008, in Sparks (Reno), Nevada. In 2006, the U.S. Geological Survey (USGS) initiated a study of the diverse and uncommon mineral resources associated with carbonatites and associated alkaline igneous rocks. Most of these deposit types have not been studied by the USGS during the last 25 years, and many of these mineral resources have important applications in modern technology. The author chose to begin this study at Iron Hill in southwestern Colorado because it is the site of a classic carbonatite complex, which is thought to host the largest known resources of titanium and niobium in the United States.

Colorado↗

Petrologic, tectonic, and metallogenic evolution of the Ancestral Cascades magmatic arc, Washington, Oregon, and northern California

Present-day High Cascades arc magmatism was preceded by ∼40 m.y. of nearly cospatial magmatism represented by the ancestral Cascades arc in Washington, Oregon, and northernmost California (United States). Time-space-composition relations for the ancestral Cascades arc have been synthesized from a recent compilation of more than 4000 geochemical analyses and associated age data. Neither the composition nor distribution of ancestral Cascades magmatism was uniform along the length of the ancestral arc through time. Initial (>40 to 36 Ma) ancestral Cascades magmatism (mostly basalt and basaltic andesite) was focused at the north end of the arc between the present-day locations of Mount Rainier and the Columbia River. From 35 to 18 Ma, initial basaltic andesite and andesite magmatism evolved to include dacite and rhyolite; magmatic activity became more voluminous and extended along most of the arc. Between 17 and 8 Ma, magmatism was focused along the part of the arc coincident with the northern two-thirds of Oregon and returned to more mafic compositions. Subsequent ancestral Cascades magmatism was dominated by basaltic andesite to basalt prior to the post–4 Ma onset of High Cascades magmatism. Transitional tholeiitic to calc-alkaline compositions dominated early (before 40 to ca. 25 Ma) ancestral Cascades eruptive products, whereas the majority of the younger arc rocks have a calc-alkaline affinity. Tholeiitic compositions characteristic of the oldest ancestral arc magmas suggest development associated with thin, immature crust and slab window processes, whereas the younger, calc-alkaline magmas suggest interaction with thicker, more evolved crust and more conventional subduction-related magmatic processes. Presumed changes in subducted slab dip through time also correlate with fundamental magma composition variation. The predominance of mafic compositions during latest ancestral arc magmatism and throughout the history of modern High Cascades magmatism probably reflects extensional tectonics that dominated during these periods of arc magmatism. Mineral deposits associated with ancestral Cascades arc rocks are uncommon; most are small and low grade relative to those found in other continental magmatic arcs. The small size, low grade, and dearth of deposits, especially in the southern two-thirds of the ancestral arc, probably reflect many factors, the most important of which may be the prevalence of extensional tectonics within this arc domain during this magmatic episode. Progressive clockwise rotation of the forearc block west of the evolving Oregon part of the ancestral Cascades magmatism produced an extensional regime that did not foster significant mineral deposit formation. In contrast, the Washington arc domain developed in a transpressional to mildly compressive regime that was more conducive to magmatic processes and hydrothermal fluid channeling critical to deposit formation. Small, low-grade porphyry copper deposits in the northern third of the ancestral Cascades arc segment also may be a consequence of more mature continental crust, including a Mesozoic component, beneath Washington north of Mount St. Helens.

California, Oregon, Washington↗

Application of ultraviolet reflectance and stimulated luminescence to the remote detection of natural materials

Carbonate rocks and evaporite deposits commonly exhibit relatively high reflectance in the ultraviolet (<3600A), and some outcrops of these materials are selectively shown on ultraviolet imagery. Other materials which are commonly strongly imaged on ultraviolet imagery and photography include water, snow, concrete, and metallic objects, particularly aluminum. Outdoor tests of an active ultraviolet imaging system have demonstrated the feasibility of imaging ultraviolet stimulated luminescence of such minerals as talc, dolomite, and deweylite along quarry faces from distances of several hundred feet. The system features a cathode ray tube transmitter, an image dissector receiver, and a video monitor on which the distribution of luminescent material is imaged as the outcrop is scanned. A pulsed ultraviolet laser emitting at 3371A has been used successfully in the laboratory to stimulate phosphorescence of selected rock and mineral specimens and to discriminate between them on the basis of decay time which ranges from less than three to more than 10 microseconds. Initial results suggest that sodic feldspars have longer decay periods than calcic feldspars. Some granites also appear to have decay periods significantly different from other types of granite in the same locality. Outdoor tests with a high-resolution grating spectrometer were successful in detecting luminescent materials by means of the so-called "Fraunhofer line-depth method". This method is advantageous because it uses the sun so an ultraviolet source and therefore ifs independent of low-powered artificial sources such as cathode ray tubes, lasers, and mercury vapor lamps„ A Fraunhofer line- discriminator suitable for aircraft operation has been constructed, and initial on-the- ground tests are being performed on Rhodamine WT, a luminescent dye used by hydrologists and oceanographers in studies of current dynamics in streams and estuaries.

Open-File Report↗

A reconnaissance for signs of a Mississippi Valley-type lead-zinc mineralizing system on the eastern flank of the Rutbah Uplift, Anbar Province, Iraq

Reconnaissance field visits and rock sampling were conducted at eight geologically selected locations within Mesozoic rocks on the eastern flank of the Rutbah Uplift, Anbar Province, western Iraq, in an attempt to determine if these rocks have been affected by a Mississippi Valley-Type (MVT) lead-zinc mineralizing system. Samples subsequently were studied by carbonate mineral staining, transmitted and reflected light petrology, and scanning electron microscopy with semi-quantitative energy dispersive elemental analyses. Single samples were studied by each, inductively coupled plasma mass spectrometry analyses of trace elements and fluid inclusion microthermometry. Permissive evidence indicates that there has been a MVT system present, but none of the evidence is considered definitive.

Anbar Province↗

Origin and significance of postore dissolution collapse breccias cemented with calcite and barite at the Meikle gold deposit, Northern Carlin trend, Nevada

The final event in a complicated hydrothermal history at the Meikle gold deposit was gold deficient but caused extensive postore dissolution of carbonate, collapse brecciation, and precipitation of calcite and barite crystals in the resulting cavities. Although previously interpreted to be part of the Carlin -type hydrothermal system, crosscutting relationships and U-Th-Pb geochronology constrain this hydrothermal event to late Pliocene time (ca. 2 Ma), nearly 36 Ma after ore formation. Mineralogic, fluid inclusion, and stable isotope data indicate that postore hydrothermal fluids were reduced, H 2 S-rich, unevolved meteoric waters ((δ 18 O = -17‰) of low temperature (ca. 65°C). The δ 18 O values of barite and calcite indicate that these minerals were in isotopic equilibrium, requiring that barite SO 4 was derived from the oxidation of reduced sulfur; however, preexisting sulfides in breccia cavities were not oxidized. The δ 34 S (15‰) values of barite are higher than those of local bulk sulfide and supergene alunite indicating that SO 4 was not derived from supergene oxidation of local sulfide minerals. The 15 per mil δ 34 S value suggests that the H 2 S in the fluids may have been leached from sulfur-rich organic matter in the local carbonaceous sedimentary rocks. A reduced H 2 S-rich fluid is also supported by the bright cathodoluminescence of calcite which indicates that it is Mn rich and Fe poor. Calcite has a narrow range of δ 13 C values (0.3-1.8‰) that are indistinguishable from those of the host Bootstrap limestone, indicating that CO 2 in the fluid was from dissolution of the local limestone. These data suggest that dissolution and brecciation of the Bootstrap limestone occurred where H 2 S-rich fluids encountered more oxidizing fluids and formed sulfuric acid (H 2 SO 4 ). Intense fracturing in the mine area by previous structural and hydrothermal events probably provided conduits for the descent of oxidized surface water which mixed with the underlying H 2 S-rich waters to form the dissolving acid. The surface-derived fluid apparently contained sufficient oxygen to produce H 2 SO 4 from H 2 S but not enough to alter pyrite to Fe oxide. Although H 2 S is an important gold -transporting ligand, the temperature was too low to transport a significant amount of gold . The presence of analogous calcite - and barite -lined cavities in other Carlin -type deposits suggests that the generation (and oxidation) of H 2 S-rich meteoric waters was a common phenomenon in north-central Nevada . Previous sulfur isotope studies have also shown that the Paleozoic sedimentary rocks were the principal source of H 2 S in Devonian sedimentary exhalative-type, Jurassic intrusion-related, Eocene Carlin -type, and Miocene low-sulfidation gold deposits in the region. The similar sulfur source in all of these systems suggests that basin brines, magmatic fluids, and meteoric waters all evolved to be H 2 S-rich ore fluids by circulation through Paleozoic sedimentary rocks. Thus, although not directly related to gold mineralization, the recent hydrologic history of the deposit provides important clues to earlier ore-forming processes that were responsible for gold mineralization.

Nevada↗

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

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

Nevada↗

Mineral resources of Du Noir Addition, Washakie Wilderness area, Fremont County, Wyoming

The Du Noir Addition to the Washakie Wilderness area consists of 34,200 acres (13,840 hectares) of scenic mountainous terrain that adjoins the Teton Wilderness and Washakie Wilderness areas. The area was studied in 1973 by the U.S. Geological Survey and U.S. Bureau of Mines to evaluate its mineral, fuel, and geothermal energy potential. This evaluation is based on a search of the geologic literature, claim and production records, and fieldwork including mapping, inspection of claims and prospects, interpretation of aeromagnetic maps, and analyses of bedrock and stream-sediment samples. Flat-lying Eocene volcaniclastic rocks of the Absaroka volcanic field are exposed in about two-thirds of the Du Noir Addition. These volcanics unconformably overlie the deeply eroded, northwest-trending Du Noir anticline in which Paleozoic marine strata of Devonian through Permian age are exposed. Of lesser importance are small deposits of Eocene non-volcanic conglomerate, and basaltic intrusive and extrusive rocks of late Pliocene and possibly younger age. The results of this study indicate that the mineral, fuel, and geothermal potential of the Du Noir Addition are minimal. Low-grade copper-molybdenum mineralization occurs outside the addition, associated with intrusive rocks, but no indications of alteration or mineralization were found within the study area. Anomalous, but not economically important, concentrations of molybdenum and uranium were found in Permian and Eocene carbonaceous shales. Phosphate rock in the Phosphoria Formation occurs in beds too thin to constitute a resource. Large amounts of very pure limestone are present in the Madison Limestone, but equally pure limestone, much closer to transportation facilities, is found throughout this part of Wyoming. That part of the Du Noir anticline in the addition is too deeply eroded to be a likely reservoir of oil and gas. Present data indicates a low potential for geothermal energy in or near the addition.

Wyoming↗

Mineral resource potential map of the Natural Area Roadless Area, Baker County, Florida

The Natural Area Roadless Area, which is in the Osceola National Forest in Baker County, Fla., is underlain by sedimentary rocks containing phosphate deposits that are not a potential mineral resource by todays standards. The region has a low potential for oil and gas and virtually no potential for other valuable minerals. The phosphate deposits are either slightly low in tonnage and P 2 O 5 content, high in MgO and/or Fe 2 O 3 + Al 2 O 3 , or the ratio of CaO to P 2 O 5 is too high for deposits that can be mined profitably at the present time. A low potential for oil and gas is indicated by the numerous dry holes in the region and the absence of the formations that contain these hydrocarbons in southern and westernmost Florida. The only mineral material that has been produced in the study area is clayey sand, used in stabilizing Forest Service roads. This type of clayey sand has no particular value because there are virtually unlimited quantities in the surrounding region. The peaty material in the area is too high in ash content to be mined. Large quantities of limestone underlie the area but are too deeply buried to be quarried. Heavy-mineral and clay deposits, which are mined elsewhere in northern peninsular Florida, are not present in the study area.

Florida↗

Beryllium geochemistry in soils: Evaluation of 10Be/9Be ratios in authigenic minerals as a basis for age models

Soils contain a diverse and complex set of chemicals and minerals. Being an 'open system', both in the chemical and nuclear sense, soils have defied quantitative nuclear dating. However, based on the published studies of the cosmogenic atmospheric 10Be in soils, its relatively long half-life (1.5 Ma), and the fact that 10Be gets quickly incorporated in most soil minerals, this radionuclide appears to be potentially the most useful for soil dating. We therefore studied the natural variations in the specific activities of 10Be with respect to the isotope 9Be in mineral phases in eight profiles of diverse soils from temperate to tropical climatic regimes and evaluated the implications of the data for determining the time of formation of soil minerals, following an earlier suggestion [Lal et al., 1991. Development of cosmogenic nuclear methods for the study of soil erosion and formation rates. Current Sci. 61, 636-639.]. We find that the 10Be/9Be ratios in both bulk soils and in the authigenic mineral phases are confined within a narrower range than in 10Be concentrations. Also, the highest 10Be/9Be ratios in authigenic minerals are observed at the soil-rock interface as predicted by the model. We present model 10Be/9Be ages of the B-horizon and the corresponding soil formation rates for several soil profiles. The present study demonstrates that the 10Be/9Be ratios in the authigenic phases, e.g. clay and Fe-hydroxides, can indeed be used for obtaining useful model ages for soils younger than 10-15 Ma. However, the present work has to be pushed considerably further, to take into account more realistic age models in which, for instance, downward transport of 10Be and clays, and in-situ dissolution of clay minerals at depths, altering the 10Be/9Be ratios of the acidic solutions, are included. We show that in the case of younger soils (< 1 Ma) studied here, their 10Be inventories and 10Be/9Be ratios have been significantly disturbed possibly by mixing with transported soils. ?? 1997 Elsevier Science B.V.

Chemical Geology↗

Investigations of the characteristics, origin, and residence time of the upland residual mantle of the Piedmont of Fairfax County, Virginia

Undisturbed cores of upland regolith developed from a variety of crystalline rocks of the Piedmont province in Fairfax County, Va., have been obtained by using a combination of Shelby tubes, Denison sampler, and modified diamond core drilling. The core study correlated variations in chemistry, mineralogy, and texture with engineering properties throughout individual weathering profiles and contrasted these parameters among weathering profiles developed from various parent rocks. Coring sites were chosen to obtain a maximum depth of weathering on diverse lithologies. The rocks that were investigated included metapelite, metagraywacke, granite, diabase, and serpentinite. Four to twelve samples per core were selected for analysis of petrography, texture, clay mineralogy, and major-element chemistry. The number of samples was determined on the basis of (1) the thickness of the weathering profile (from about 1 m in serpentinite to more than 30 m in pelitic schist) and (2) megascopic changes in the weathering profile. Shear strength and compressibility were determined on corresponding segments of core. Standard penetration tests were performed adjacent to coring sites to evaluate in-place engineering properties. The regolith profiles on all rocks can be subdivided into soil, massive subsoil, saprolite, and weathered rock zones. Major differences in thicknesses of these zones are related to parent rock. Total regolith thickness is related to saprolite thickness. Saprolite is thickest on quartzofeldspathic metapelite, metagraywacke, and granite; thinner on diabase; and thinnest on serpentinite. Thickness of saprolite is related to rock structure and mineralogy. Geochemical changes of saprolite developed from each rock type follow predictable trends from fresh rock to soil profile, with increases in Ti, AI, Fe 3 +, and H 2 0+relative to absolute losses of Si, Fe2+, Mg, Ca, and Na. These variations are more pronounced in the weathering profiles above mafic and ultramafic rocks than in those above metagraywacke. Clay minerals in granite, schist, and metagraywacke saprolites are kaolinite, dioctahedral vermiculite, interlayered mica-vermiculite, and minor illite. Gibbsite is developed in near-surface samples of schist. Standard penetration test data for the upper 7 m of saprolite above schist, metagraywacke, and granite suggest alternations between stronger and weaker horizons that correlate with megascopic ally identified zones: soil, massive subsoil, and saprolite. The data correlate with density. Shear strength increases fairly regularly downward in the weathering profile. The engineering behavior of diabase saprolite is controlled by a dense, plastic, near-surface clay layer (montmorillonite and kaolinite) overlying rock that is weathered to a granular state (grus); the engineering properties of serpentinite are controlled by a very thin weathering profile. Similarities in regolith thickness, zonation, mineralogy, and chemistry of quartzofeldspathic rocks indicate the existence of fundamental geochemical and geomechanical controls on regolith evolution on the Piedmont upland. Data from the profiles of quartzofeldspathic regolith are used to construct a model suggesting the principal rate-control steps in the development and downwasting of the upland regolith. This model is consistent with available information about Piedmont hydrology and tectonic uplift.

Professional Paper↗