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At least 1,027 records · Page 57Linked to original sources

Radioactivity at the Copper Creek copper lode prospect, Eagle district, east-central Alaska

Investigation of radioactivity anomalies at the Copper Creek copper lode prospect, Eagle district, east-central Alaska, during 1949 disclosed that the radioactivity is associated with copper mineralization in highly metamorphosed sedimentary rocks. These rocks are a roof pendant in the Mesozoic "Charley River" batholith. The radioactivity is probably all due to uranium associated with bornite and malachite.

Alaska↗

Unravelling the structural control of mississippi valley-type deposits and prospects in carbonate sequences of the Western Canada Sedimentary Basin

Re-examination of selected MVT outcrops and cores in the Interior Plains and Rocky Moun-tains of Alberta, corroborated with previous paragenetic, isotopic and structural data, suggests Laramide structural channelling of dolomitizing and mineralizing fluids into strained carbonate rocks. At Pine Point, extensional faults underlying the trends of MVT ore bodies and brittle faults overprinting the Great Slave Lake Shear Zone define apinnate fault geometry and appear to be kinematically linked. Chemical and isotopic characteristics of MVT parental fluids are consistent with seawater and brine convection within fault-confined verticalaquifers, strong water-basement rock interaction, metalleaching from the basement, and focused release of hydrothermal fluids within linear zones of strained carbonate caprocks. Zones of recurrent strain in the basement and a cap of carbonate strata constitute the critical criteria for MVTexploration target selection in the WCSB.

Bulletin of the Geological Survey of Canada↗

Water chemistry at Snowshoe Mountain, Colorado: mixed processes in a common bedrock

At Snowshoe Mountain the primary bedrock is quite homogeneous, but weathering processes vary as waters moves through the soils, vadose zone and phreatic zone of the subsurface. In the thin soil, physical degradation of tuff facilitates preferential dissolution of potassium ion from glass within the rock matrix, while other silicate minerals remain unaltered. In the vadose zone, in the upper few meters of fractured bedrock, dilute water infiltrates during spring snowmelt and summer storms, leading to preferential dissolution of augite exposed on fracture surfaces. Deeper yet, in the phreatic zone of the fractured bedrock, Pleistocene calcite fracture fillings dissolve, and dioctahedral and trioctahedral clays form as penetrative weathering alters feldspar and pyroxene. Alkalinity is generated and silica concentrations are buffered by mineral alteration reactions.

Colorado↗

A case of Te-rich low-sulfidation epithermal Au-Ag deposits in a calc-alkaline magmatic arc, NE China

Tellurium-bearing low-sulfidation epithermal Au-Ag deposits are significant producers of gold, silver, and potentially strategic elements if mineral processing methods are optimized for recovery. Although these deposits are generally related to alkaline magmatism, our study documents an unusual occurrence of Te-rich low-sulfidation epithermal systems in the North Heilongjiang Belt in northeast China that is spatially and temporally associated with calc-alkaline magmatism and tectonic extension in a continental arc‐setting. In the North Heilongjiang Belt, Te-bearing Au-Ag deposits are usually sited in dilatant zones, mostly along extensional NW structures or at their intersections with deep‐seated NE-striking faults such as the Nenjiang-Heihe and Jiayin-Mudanjiang lineaments. Of these deposits, Sandaowanzi is well‐known for its bonanza gold grades. These faults localized andesitic to rhyolitic volcano-plutonic centers that evolved from mantle‐derived mafic melts to intermediate compositions due to differentiation and crustal assimilation as documented by their mineralogy and Sr, Nd, and Pb isotope compositions. During assimilation of country rocks, fluids containing 3 He and other volatiles derived from mantle magmas displaced or mixed with external groundwater containing radiogenic 4 He derived from country rocks. In this belt, the bulk metal content of Au, Ag and Te was probably introduced by deep mantle‐derived mafic‐intermediate calc‐alkaline intrusions. However, our study does not exclude input of metals leached from underlying metasedimentary rocks and older Te‐bearing Au mineralization. The noble gas, hydrogen, oxygen and lead isotope compositions of fluid inclusions and ore minerals suggest that the deposits formed by mixing between magmatic fluids and convecting meteoric ground waters containing lead leached from surrounding country rocks. At deeper levels, isotopic evidence suggests that Au-Ag-Te (Bi) precipitated with pyrite, quartz, sericite, and carbonate minerals due to mixing with Te-rich fluids. At shallower levels, Au and Ag precipitated contemporaneously with base‐metal sulfides, hydrothermal quartz and sericite during episodic boiling as evidenced by silica morphology and mineral textures. The relatively uniform spacing of epithermal systems along NW- and NE-trending structures in the North Heilongjiang Belt was used to identify unexplored spaces within this mineral belt that are prospective for concealed low-sulfidation epithermal gold deposits. Although some of the Au-Ag deposits in this belt are enriched in Te, there is a lack of coeval alkaline igneous rocks that are commonly associated with Te-bearing gold deposits elsewhere in the world (e.g., Cripple Creek, Emperor, and Lihir Island).

North Heilongjiang Belt↗

Hydrothermal alteration mineralogy of SOH drill holes, Kilauea East Rift Zone geothermal area, Hawaii

Thirty-eight hydrothermal minerals were identified from 356 drill-core specimens that were obtained from three Scientific Observation Holes (SOH-1, SOH-2, and SOH-4) drilled along the lower East Rift Zone (ERZ) of Kilauea Volcano, Hawaii. The minerals formed during alteration of basaltic rocks and glass by hot, circulating, waters in aquifers consisting of variable mixtures of meteoric water and sea water. Several zeolites, hydrated calcium silicates, carbonates, clays, silicates, sulfates, sulfides, and other minerals were found filling open spaces of vesicles, fractures, and between breccia fragments of the recovered drill core; many specimens that originally consisted of glass are completely altered to some of these minerals, especially clays. Several hydrothermal minerals (erionite, mordenite, truscottite, smectite, chlorite-smectite, chalcedony, anhydrite, and hematite), occur in the SOH drill holes at higher measured temperatures than the same minerals are found in geothermal drill holes of Iceland or other geothermal areas, suggesting that temperatures within the ERZ geothermal system have increased since the minerals formed. Fluid-inclusion freezing data for quartz, anhydrite, and calcite from the three SOH holes show that composition of the inclusion fluids ranges from dilute meteoric water to highly modified sea water concentrated by boiling. Comparison of measured drill-hole temperatures with fluid-inclusion homogenization-temperature data indicates that only about 15% of the fluid inclusions could have formed under the present thermal conditions. The majority of fluid inclusions studied apparently formed during one or more temperature fluctuations associated with the emplacement of nearby dikes and their subsequent cooling. Bacteria-like particles at 1734.6 m depth in SOH-4 could be very significant because the particles occurred at much hotter temperatures (about 265°C) than the generally accepted 110°C limit for survival of bacteria. The presence of Cl in the particles suggests that they might have lived in a saline environment and did not result from contamination by the fresh water drilling fluids. We reccomend that future drilling and subsequent handling of drill hole specimens in the ERZ and elsewhere employ controls to minimize and(or) recognize bacterial contamination.

Open-File Report↗

Compositional and mineralogic constraints on the genesis of ophiolite hosted nickel mineralization in the Pevkos area, Limassol Forest, Cyprus

Mineralization composed dominantly of primary troilite, maucherite, pentlandite, and chalcopyrite, and secondary valleriite occurs in serpentinized transition zone rocks of the Limasol Forest segment of the Troodos ophiolite complex, Cyprus. Whole-rock and electron microprobe analyses of this mineralization gives ranges of Cu/(Cu+Ni)=0.16 to 0.47, Pt/(Pt+Pd)=0.66 to 0.51, Ni/Co=6.33 to 13.4, and chondrite normalized plots with low concentrations of Rh, Pt, and Pd, but relatively high Au. Estimated distribution coefficients of nickel and iron between olivine and ore range from 0.5 to 7.4. Most of these data are unlike values from magmatic sulfide deposits and indicate either a complete alteration of a preexisting magmatic sulfide concentration or, more likely, a nonmagmatic origin for this mineralization. ?? 1985 Springer-Verlag.

Mineralium Deposita↗

Carbonatites: A review

The carbonatites are essentially carbonate-silicate rock with a great variety of other minerals. In this review the writer stresses the field and geochemical relationships of the carbonatites and alkalic igneous rocks and concludes that carbonatites were deposited by carbonatic solutions having a wide range of temperature, pressure, and concentration and derived from alkalic magmas during the process of silicate crystallization. Brogger's concept of carbonate magma is evaluated in the light of more recent field and laboratory investigations, and the conclusion is reached that a carbonate magma in the normal sense is less likely to exist than carbonate-rich solutions which at elevated temperature and pressure can have a higher concentration of dissolved ingredients than normally believed for hydrothermal solutions. At many localities the carbonatites occur as veinlike or dikelike bodies or as cores in volcanic plugs of alkalic rocks. Recent investigations indicate that the carbonatites and related alkalic rocks represent a relatively unevaluated category of ore deposits that contain an impressive reserve of such rare commodities as niobium (columbium), titanium, zirconium, rare earths, barium, strontium, uranium, magnetite, phosphate, vermiculite, and agricultural lime.

GSA Bulletin↗

New techniques for the quantification and modeling of remotely sensed alteration and linear features in mineral resource assessment studies

Linear structural features and hydrothermally altered rocks that were interpreted from Landsat data have been used by the U.S. Geological Survey (USGS) in regional mineral resource appraisals for more than a decade. In the past, linear features and alterations have been incorporated into models for assessing mineral resources potential by manually overlaying these and other data sets. Recently, USGS research into computer-based geographic information systems (GIS) for mineral resources assessment programs has produced several new techniques for data analysis, quantification, and integration to meet assessment objectives.

Pecora XI Symposium↗

Differentiation and magma mixing on Kilauea's east rift zone: A further look at the eruptions of 1955 and 1960. Part II. The 1960 lavas

New and detailed petrographic observations, mineral compositional data, and whole-rock vs glass compositional trends document magma mixing in lavas erupted from Kilauea's lower east rift zone in 1960. Evidence includes the occurrence of heterogeneous phenocryst assemblages, including resorbed and reversely zoned minerals in the lavas inferred to be hybrids. Calculations suggest that this mixing, which is shown to have taken place within magma reservoirs recharged at the end of the 1955 eruption, involved introduction of four different magmas. These magmas originated beneath Kilauea's summit and moved into the rift reservoirs beginning 10 days after the eruption began. We used microprobe analyses of glass to calculate temperatures of liquids erupted in 1955 and 1960. We then used the calculated proportions of stored and recharge components to estimate the temperature of the recharge components, and found those temperatures to be consistent with the temperature of the same magmas as they appeared at Kilauea's summit. Our studies reinforce conclusions reached in previous studies of Kilauea's magmatic plumbing. We infer that magma enters shallow storage beneath Kilauea's summit and also moves laterally into the fluid core of the East rift zone. During this process, if magmas of distinctive chemistry are present, they retain their chemical identity and the amount of cooling is comparable for magma transported either upward or laterally to eruption sites. Intrusions within a few kilometers of the surface cool and crystallize to produce fractionated magma. Magma mixing occurs both within bodies of previously fractionated magma and when new magma intersects a preexisting reservoir. Magma is otherwise prevented from mixing, either by wall-rock septa or by differing thermal and density characteristics of the successive magma batches.

Bulletin of Volcanology↗

Results of a geochemical survey, Aban Al Ahmar Quadrangle, Sheet 25F, Kingdom of Saudi Arabia

The interpretation of geochemical data from a regional survey of the Aban al Ahmar quadrangle resulted in the selection of areas for follow-up studies. The results of detailed geochemical studies of these areas, combined with field observation, resulted in the selection of areas of moderate to high mineral resource potential. The most important areas are (1) the Jibal Minyah area, Aban al Asmar area, Jibal Suwaj area, and Nubayah area where tin and tungsten mineralization are associated with Abanat-suite rocks or possible buried Abanat-suite plutons; (2) several areas containing rocks of the Murdama group in the northern part of the quadrangle, the Buqaya al Luaah area, and the Jabal Akkash area where precious- and base-metal mineralization are generally associated with small Idah-suite plutons; and (3) the southern periphery of Jibal Qitan associated with skarn mineralization. The Aban al Ahmar quadrangle (sheet 25F) lies in the northeastern part of the Proterozoic Arabian Shield. Plots showing the distribution of single elements and factor scores of the regional geochemical data for wadi concentrates were used to select favorable areas for follow-up work. Detailed follow-up studies consisted of the collection of samples of rocks, wadi concentrates, and wadi sediments. The most useful pathfinder elements for precious- and base-metal mineralization are Cu and Pb, and for tin and tungsten mineralization they are Sn, La, Nb, Y, and Be. R-mode factor analysis of the regional geochemical data resulted in two factors that reflect mineralization: precious- and base-metal mineralization; and Abanat-suite lithology and, therefore, tin and tungsten mineralization. A major problem in the interpretation of the regional geochemical data resulted from incomplete removal of magnetite from the samples prior to analysis. The presence of magnetite can cause anomalous values of Ni, Fe, V, Cu, and Co in samples because of it's ability to incorporate these elements into its structure during magmatic crystallization.

Open-File Report↗

Mesozoic magmatism and base-metal mineralization in the Fortymile mining district, eastern Alaska — Initial results of petrographic, geochemical, and isotopic studies in the Mount Veta area

We present here the initial results of a petrographic, geochemical, and isotopic study of Mesozoic intrusive rocks and spatially associated Zn-Pb-Ag-Cu-Au prospects in the Fortymile mining district in the southern Eagle quadrangle, Alaska. Analyzed samples include mineralized and unmineralized drill core from 2006 and 2007 exploration by Full Metal Minerals, USA, Inc., at the Little Whiteman (LWM) and Fish prospects, and other mineralized and plutonic samples collected within the mining district is part of the USGS study. Three new ion microprobe U-Pb zircon ages are: 210 ± 3 Ma for quartz diorite from LWM, 187 ± 3 Ma for quartz monzonite from Fish, and 70.5 ± 1.1 Ma for altered rhyolite porphyry from Fish. We also present 11 published and unpublished Mesozoic thermal ionization mass spectrometric U-Pb zircon and titanite ages and whole-rock geochemical data for the Mesozoic plutonic rocks. Late Triassic and Early Jurassic plutons generally have intermediate compositions and are slightly foliated, consistent with synkinematic intrusion. Several Early Jurassic plutons contain magmatic epidote, indicating emplacement of the host plutons at mesozonal crustal depths of greater than 15 km. Trace-element geochemical data indicate an arc origin for the granitoids, with an increase in the crustal component with time. Preliminary study of drill core from the LWM Zn-Pb-Cu-Ag prospect supports a carbonate-replacement model of mineralization. LWM massive sulfides consist of sphalerite, galena, and minor pyrite and chalcopyrite, in a gangue of calcite and lesser quartz; silver resides in Sb-As-Ag sulfosalts and pyrargyrite, and probably in submicroscopic inclusions within galena. Whole-rock analyses of LWM drill cores also show elevated In, an important metal in high-technology products. Hypogene mineralized rocks at Fish, below the secondary Zn-rich zone, are associated with a carbonate host and also may be of replacement origin, or alternatively, may be a magnetite-bearing Zn skarn. Cu-Zn-Pb-Ag-Au showings at the Oscar pros-pect occur in marble-hosted magnetite and pyrrhotite skarn that is spatially related to the stocks, dikes, and sills of the Early Jurassic syenite of Mount Veta. Mineralized rocks at the Eva Creek Ag-Zn-Pb-Cu prospect are within 1.5 km of the Mount Veta pluton, which is epidotized and locally altered along its contact with metamorphosed country rock east of the prospect. We report five new sulfide Pb-isotopic analyses from the LWM, Oscar, and Eva Creek prospects and compare these sulfide Pb-isotopic ratios with those for sulfides from nearby deposits and prospects in the Yukon-Tanana Upland and with feldspar Pb-isotopic ratios for Mesozoic plutons in the region. Disparities between the Pb-isotopic ratios for sulfides and igneous feldspars are consistent with a carbonate-replacement model for both the LWM and Eva Creek prospects. The presence in the Fortymile district of base-metal sulfides within both calc-silicate-rich skarns and the calc-silicate-free carbonate replacement deposits may reflect multistage mineralization by magmatic-hydrothermal systems during the emplacement of two or more magmatically unrelated igneous intrusions. Alternatively, all of the mineralized occurrences could be products of one regionally zoned system that formed during the intrusion of a single pluton. In addition to the likely origin of some of the base-metal occurrences by intrusion-related hydrothermal fluids, proximity of the LWM prospect to the northeast-striking, high-angle Kechumstuk Fault suggests that fluid flow along the fault also played an important role during carbonate-replacement mineralization.

Alaska↗

Similarities, differences, and some genetic problems of the Wyoming and Colorado plateau types of uranium deposits in sandstone

Uranium deposits of the Wyoming roll type and the Colorado Plateau peneconcordant type are the principal domestic resources of uranium. Both types occur in lenticular sandstone beds of continental origin, have a similar suite of elements and minerals, are associated with mildly altered rock, and are thought to have formed by reduction precipitation from ground waters before significant regional deformation. They differ in several respects. The Wyoming deposits are in unlithified sandstone that is highly arkosic, whereas the Colorado Plateau deposits are in lithified sandstone that is only slightly to moderately arkosic. Uranium is the only ore metal in the Wyoming deposits, whereas vanadium or copper is more abundant than uranium in some of the Plateau deposits. The Wyoming deposits are elongate crescent-shaped bodies that extend vertically through, or partly through, a sandstone unit and which are scattered, like widely spaced beads on a string, along miles-long interfaces between oxidized (altered) and unoxidized sandstone, whereas the Plateau deposits are thin tabular layers that are nearly concordant to bedding and which occur as discrete bodies, like raisins in raisin bread, enveloped in rock altered by reduction. The Wyoming ore rolls and interfaces were dynamic, having been pushed downdip by downward-moving oxygen-bearing water that passed through the interfaces and deposited the ore minerals on the reducing side, whereas the Plateau deposits seemingly formed as static bodies, localized by intensive reducing "patches" in a mildly reducing environment. These differences focus attention on genetic problems relating to the Eh of the ore-bearing and altering solutions, the shape and localization of deposits, and the source of the uranium.

Arizona, Colorado, New Mexico, South Dakota, Utah,↗

Genesis of ore deposits in the San Juan Volcanic Field, Southwestern Colorado-lead isotope evidence

In the San Juan volcanic area of southwestern Colorado, the isotopic composition of lead in ores and ore prospects of Cenozoic age ranges widely: 17.72 to 21.13 for 206 Pb/ 204 Pb; 15.50 to 15.81 for 207 Pb/ 204 Pb; and 37.21 to 38 for 208 Pb/ 204 Pb. Examination of the lead isotope data indicates that once deposition of lead minerals begins, further exchange of lead between fluid and wall rock is insignificant. This conclusion is supported by the relatively constant isotopic composition of the lead in these ores, which is not affected by the grade of ore mineralization or type of wall rock. The values of 206 Pb/ 204 Pb in some vein-type deposits exceed the maximum value known for all Mesozoic and Cenozoic igneous rocks of the Rocky Mountain region. These isotopic relations show that if ore-forming solutions are composed of meteoric water, as indicated in studies of light stable isotopes, they must have penetrated deep enough to acquire lead from Pre-cambrian rocks or sediments derived from them. The fact that some of these vein ores are now in Cenozoic igneous rocks indicates the ore fluid had an upward vertical component to its movement. The lead isotope data therefore support a circulating cell hypothesis for these kinds of ores, as suggested by many recent studies of light stable isotopes as related to mineralization. Some other deposits (Summitville, Jasper, Red Mountain district) have values of 206 Pb/ 204 Pb similar to those of the large volumes of altered rock that enclose them ( 206 Pb/ 204 Pb ∼ 18.5), suggesting that in places the lead may have been locally derived by leaching of the adjacent rocks or from magmatogenic fluids. When the lead isotope data are treated in detail, the rocks and galenas of the Platoro caldera complex, of the central San Juan caklera complex, and of the Baughman Creek center appear to contain significant components derived from 1,400- to l,500-m.y.-old and 1,700- to 1,800 m.y.-old source materials. These also are the ages of the two main groups of rocks that comprise the Precambrian basement under the San Juan volcanic area. Although the data from the western San Juan caldera complex scatter considerably, the only obvious source for the lead seems to be the 1,700- to l,800-m.y.-old rocks or detritus of such age in Phanerozoic sediments. Where the involvement of 1,400- to l,500-m.y.-old sources is greatest, the Th/U ratio in the source material is small (calculated to be about 0.7), whereas the Th/U ratio of the 1,700- to l,800-m.y.-old source material appears to be 2.3 to 3.3. The largest Th/U values are from the western San Juan caldera complex. © 1979 Society of Economic Geologists, Inc.

Colorado↗

Reconstruction of an early Permian, sublacustrine magmatic-hydrothermal system: Mount Carlton epithermal Au-Ag-Cu deposit, northeastern Australia

The Mt. Carlton Au-Ag-Cu deposit, northern Bowen basin, northeastern Australia, is an uncommon example of a sublacustrine hydrothermal system containing economic high-sulfidation epithermal mineralization. The deposit formed in the early Permian and comprises vein- and hydrothermal breccia-hosted Au-Cu mineralization within a massive rhyodacite porphyry (V2 open pit) and stratabound Ag-barite mineralization within volcano-lacustrine sedimentary rocks (A39 open pit). These orebodies are all associated with extensive advanced argillic alteration of the volcanic host rocks. Stable isotope data for disseminated alunite ( δ 34 S = 6.3–29.2‰; δ 18 OSO 4 = –0.1 to 9.8‰; δ 18 O OH = –15.3 to –3.4‰; δ D = –102 to –79‰) and pyrite ( δ 34 S = –8.8 to –2.7‰), and void-filling anhydrite ( δ 34 S = 17.2–19.2‰; δ 18 O SO4 = 1.8–5.7‰), suggest that early advanced argillic alteration formed within a magmatic-hydrothermal system. The ascending magmatic vapor ( δ 34 S ΣS ≈ –1.3‰) was absorbed by meteoric water (~50–60% meteoric component), producing an acidic (pH ≈ 1) condensate that formed a silicic → quartz-alunite → quartz-dickite-kaolinite zoned alteration halo with increasing distance from feeder structures. The oxygen and hydrogen isotope compositions of alunite-forming fluids at Mt. Carlton are lighter than those documented at similar deposits elsewhere, probably due to the high paleolatitude (~S60°) of northeastern Australia in the early Permian. Veins of coarse-grained, banded plumose alunite ( δ 34 S = 0.4– 7.0‰; δ 18 O SO4 = 2.3–6.0‰; δ 18 O OH = –10.3 to –2.9‰; δ D = –106 to –93‰) formed within feeder structures during the final stages of advanced argillic alteration. Epithermal mineralization was deposited subsequently, initially as fracture- and fissure-filling, Au-Cu–rich assemblages within feeder structures at depth. As the mineralizing fluids discharged into lakes, they produced syngenetic Ag-barite ore. Isotope data for ore-related sulfides and sulfosalts ( δ 34 S = –15.0 to –3.0‰) and barite ( δ 34 S = 22.3–23.8‰; δ 18 O SO4 = –0.2 to 1.3‰), and microthermometric data for primary fluid inclusions in barite (Th = 116°– 233°C; 0.0–1.7 wt % NaCl), are consistent with metal deposition at temperatures of ~200 ± 40°C (for Au-Cu mineralization in V2 pit) and ~150 ± 30°C (Ag mineralization in A39 pit) from a low-salinity, sulfur- and metal-rich magmatic-hydrothermal liquid that mixed with vapor-heated meteoric water. The mineralizing fluids initially had a high-sulfidation state, producing enargite-dominated ore with associated silicification of the early-altered wall rock. With time, the fluids evolved to an intermediate-sulfidation state, depositing sphalerite- and tennantite-dominated ore mineral assemblages. Void-filling massive dickite ( δ 18 O = –1.1 to 2.1‰; δ D = –121 to –103‰) with pyrite was deposited from an increasingly diluted magmatic-hydrothermal liquid (≥70% meteoric component) exsolved from a progressively degassed magma. Gypsum ( δ 34 S = 11.4–19.2‰; δ 18 O SO4 = 0.5–3.4‰) occurs in veins within postmineralization faults and fracture networks, likely derived from early anhydrite that was dissolved by circulating meteoric water during extensional deformation. This process may explain the apparent scarcity of hypogene anhydrite in lithocaps elsewhere. While the Mt. Carlton system is similar to those that form subaerial high-sulfidation epithermal deposits, it also shares several key characteristics with magmatic-hydrothermal systems that form base and precious metal mineralization in shallow-submarine volcanic arc and back-arc settings. The lacustrine paleosurface features documented at Mt. Carlton may be useful as exploration indicators for concealed epithermal mineralization in similar extensional terranes elsewhere.

Economic Geology↗

Miocene magmatism in the Bodie Hills volcanic field, California and Nevada: A long-lived eruptive center in the southern segment of the ancestral Cascades arc

The Middle to Late Miocene Bodie Hills volcanic field is a >700 km 2 , long-lived (∼9 Ma) but episodic eruptive center in the southern segment of the ancestral Cascades arc north of Mono Lake (California, U.S.). It consists of ∼20 major eruptive units, including 4 trachyandesite stratovolcanoes emplaced along the margins of the field, and numerous, more centrally located silicic trachyandesite to rhyolite flow dome complexes. Bodie Hills volcanism was episodic with two peak periods of eruptive activity: an early period ca. 14.7–12.9 Ma that mostly formed trachyandesite stratovolcanoes and a later period between ca. 9.2 and 8.0 Ma dominated by large trachyandesite-dacite dome fields. A final period of small silicic dome emplacement occurred ca. 6 Ma. Aeromagnetic and gravity data suggest that many of the Miocene volcanoes have shallow plutonic roots that extend to depths ≥1–2 km below the surface, and much of the Bodie Hills may be underlain by low-density plutons presumably related to Miocene volcanism. Compositions of Bodie Hills volcanic rocks vary from ∼50 to 78 wt% SiO 2 , although rocks with <55 wt% SiO 2 are rare. They form a high-K calc-alkaline series with pronounced negative Ti-P-Nb-Ta anomalies and high Ba/Nb, Ba/Ta, and La/Nb typical of subduction-related continental margin arcs. Most Bodie Hills rocks are porphyritic, commonly containing 15–35 vol% phenocrysts of plagioclase, pyroxene, and hornblende ± biotite. The oldest eruptive units have the most mafic compositions, but volcanic rocks oscillated between mafic and intermediate to felsic compositions through time. Following a 2 Ma hiatus in volcanism, postsubduction rocks of the ca. 3.6–0.1 Ma, bimodal, high-K Aurora volcanic field erupted unconformably onto rocks of the Miocene Bodie Hills volcanic field. At the latitude of the Bodie Hills, subduction of the Farallon plate is inferred to have ended ca. 10 Ma, evolving to a transform plate margin. However, volcanism in the region continued until 8 Ma without an apparent change in rock composition or style of eruption. Equidimensional, polygenetic volcanoes and the absence of dike swarms suggest a low differential horizontal stress regime throughout the lifespan of the Bodie Hills volcanic field. However, kinematic data for veins and faults in mining districts suggest a change in the stress field from transtensional to extensional approximately coincident with the inferred cessation of subduction. Numerous hydrothermal systems were operative in the Bodie Hills during the Miocene. Several large systems caused alteration of volcaniclastic rocks in areas as large as 30 km 2 , but these altered rocks are mostly devoid of economic mineral concentrations. More structurally focused hydrothermal systems formed large epithermal Au-Ag vein deposits in the Bodie and Aurora mining districts. Economically important hydrothermal systems are temporally related to intermediate to silicic composition domes. Rock types, major and trace element compositions, petrographic characteristics, and volcanic features of the Bodie Hills volcanic field are similar to those of other large Miocene volcanic fields in the southern segment of the ancestral Cascade arc. Relative to other parts of the ancestral arc, especially north of Lake Tahoe in northeastern California, the scarcity of mafic rocks, relatively K-rich calc-alkaline compositions, and abundance of composite dome fields in the Bodie Hills may reflect thicker crust beneath the southern ancestral arc segment. Thicker crust may have inhibited direct ascent and eruption of mafic, mantle-derived magma, instead stalling its ascent in the lower or middle crust, thereby promoting differentiation to silicic compositions and development of porphyritic textures characteristic of the southern ancestral arc segment.

California, Nevada↗

Effects of mother lode-type gold mineralization on 187Os/188Os and platinum group element concentrations in peridotite: Alleghany District, California

Osmium isotope compositions and concentrations of Re, platinum group elements (PGE), and Au were determined for host peridotites (serpentinites and barzburgites) and hydrothermally altered ultramafic wall rocks associated with Mother Lode-type hydrothermal gold-quartz vein mineralization in the Alleghany district, California. The host peridotites have Os isotope compositions and Re, PGE, and Au abundances typical of the upper mantle at their presumed formation age during the late Proterozoic or early Paleozoic. The hydrothermally altered rocks have highly variable initial Os isotope compositions with ??os, values (% deviation of 187OS/188OS from the chondritic average calculated for the approx. 120 Ma time of mineralization) ranging from -1.4 to -8.3. The lowest Os isotope compositions are consistent with Re depletion of a chondritic source (e.g., the upper mantle) at ca. 1.6 Ga. Most of the altered samples are enriched in Au and have depleted and fractionated abundances of Re and PGE relative to their precursor peridotites. Geoehemical characteristics of the altered samples suggest that Re and some PGE were variably removed from the ultramafic rocks during the mineralization event. In addition to Re, the Pt and Pd abundances of the most intensely altered rocks appear to have been most affected by mineralization. The 187Os-depleted isotopic compositions of some altered rocks are interpreted to be a result of preferential 187Os loss via destruction of Re-rich phases during the event. For these rocks, Os evidently is not a useful tracer of the mineralizing fluids. The results do, however, provide evidence for differential mobility of these elements, and mobility of 187Os relative to the initial bulk Os isotope composition during hydrothermal metasomatic alteration of ultramafic rocks. ?? 2007 Society of Economic Geologists, Inc.

Economic Geology↗

Summaries of data on and lists of references to metallic and selected nonmetallic mineral deposits in the Talkeetna Mountains Quadrangle, Alaska

These summaries of data on metallic and selected nonmetallic mineral occurrences and lists of selected references to them in Geological Survey, U.S. Bureau of Mines, and State of Alaska Division of Geological and Geophysical Surveys (and predecessor State agencies) reports and maps are designed to aid in library research on the mineral resources of the Talkeetna Mountains quadrangle, Alaska. The references listed are selected in the sense that mainly statistical reports such as the annual Minerals Yearbook of the U.S. Bureau of Mines and many annual and biennial reports of the Alaska Division of Geological and Geophysical Surveys and its predecessor agencies are not included. Also not included are data on many claims about which little more than their locations is known (for example, localities 3 and 6 in Csejtey and Miller, 1978 (OF 78- 558B)). These omissions should not be interpreted as a judgement that the claims are not on valid mineral occurrences, but only that there are insufficient data to describe any mineral deposit that might be present. Geochemical anomalies determined by analyses of rock and stream—sediment samples in which no metallic mineral was identified are also omitted. This report is divided into three parts: a section made up of summaries of data and reference lists arranged alphabetically by occurrence name; a second section that lists synonyms for names in the first section and the names of owners and operators of mines and prospects; and a final section that lists alphabetically by author all references mentioned in the first section and in these introductory paragraphs.

Alaska↗

Summaries of data on and lists of references to metallic and selected nonmetallic mineral deposits in fifteen quadrangles in southwestern and west-central Alaska

These summaries of data on metallic and selected nonmetallic mineral occurrences and lists of selected references to them in Geological Survey, U.S. Bureau of Mines, and State of Alaska Division of Geological and Geophysical Surveys (and predecessor State and Territorial agencies) reports and maps released before Jan. 1, 1980, and in one abstract of a report presented orally at a scientific meeting, are designed to aid in library research on the mineral resources of 14 quadrangles in southwestern Alaska and the Saint Lawrence quadrangle in west—central Alaska. The references are selected in the sense that mainly statistical reports such as the annual Minerals Yearbook of the U.S. Bureau of Mines and many annual and biennial reports of the Alaska Division of Geological and Geophysical Surveys and its predecessor agencies are not included. Also not included are data on many claims about which little more than their locations is known (for example, localities 11 to 14 in MacKevett and Holloway, 1977 (OF 77-169D), p. 28). These omissions should not be interpreted as a judgement that the claims are not on valid mineral occurrences, but only that there are insufficient data to describe any mineral deposit that might be present. Geochemical anomalies determined by analyses of rock and stream—sediment samples in which no metallic mineral was identified are also omitted. Work now in progress should add greatly to the knowledge of mineral resources in several quadrangles on the Alaska Peninsula.

Alaska↗