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At least 901 records · Page 50Linked to original sources
USGS2010

Legacy of the California Gold Rush: Environmental geochemistry of arsenic in the southern Mother Lode Gold District

Gold mining activity in the Sierra Nevada foothills, both recently and during the California Gold Rush, has exposed arsenic-rich pyritic rocks to weathering and erosion. This study describes arsenic concentration and speciation in three hydrogeologic settings in the southern Mother Lode Gold District: mineralized outcrops and mine waste rock (overburden); mill tailings submerged in a water reservoir; and lake waters in this monomictic reservoir and in a monomictic lake developing within a recent open-pit mine. These environments are characterized by distinct modes of rock-water interaction that influence the local transport and fate of arsenic. Arsenic in outcrops and waste rock occurs in arsenian pyrite containing an average of 2 wt% arsenic. Arsenic is concentrated up to 1300 ppm in fine-grained, friable, iron-rich weathering products of the arsenian pyrite (goethite, jarosite, copiapite), which develop as efflorescences and crusts on weathering outcrops. Arsenic is sorbed as a bidentate complex on goethite, and substitutes for sulfate in jarosite. Submerged mill tailings obtained by gravity core at Don Pedro Reservoir contain arsenic up to 300 ppm in coarse sand layers. Overlying surface muds have less arsenic in the solid fraction but higher concentrations in porewaters (up to 500 μg/L) than the sands. Fine quartz tailings also contain up to 3.5 ppm mercury related to the ore processing. The pH values in sediment porewaters range from 3.7 in buried gypsum-bearing sands and tailings to 7 in the overlying lake sediments. Reservoir waters immediately above the cores contain up to 3.5 μg/L arsenic; lake waters away from the submerged tailings typically contain less than 1 μg/L arsenic. Dewatering during excavation of the Harvard open-pit mine produced a hydrologic cone of depression that has been recovering toward the pre-mining groundwater configuration since mining ended in 1994. Aqueous arsenic concentrations in the 80 m deep pit lake are up to 1000 μg/L. Redistribution of the arsenic occurs during summer stratification, with highest concentrations at middle depths. The total mass of arsenic in the pit lake increases coinciding with early winter rains that erode, partially dissolve, and transport arsenic-bearing salts into the pit lake. Arsenic concentration, speciation, and distribution in the Sierra Nevada foothills depend on many factors, including the lithologic sources of arsenic, climatic influences on weathering of host minerals, and geochemical characteristics of waters with which source and secondary minerals react. Oxidation of arsenian pyrite to goethite, jarosite, and copiapite causes temporary attenuation of arsenic during summer, when these secondary minerals accumulate; subsequent rapid dissemination of arsenic into the aqueous environment is caused by annual winter storms. As the population of the Mother Lode area grows, it is increasingly important to consider these effects during planning and development of land and groundwater resources.

California↗
USGS2014

Rare chemical constituents of amelia (Virginia) pegmatite dikes, and their mineral sources

Students of Igneous phenomena have long since become familiar with the occurrence of rare minerals in pegmatitic bodies. The great local concentration of rare elements in pegmatite minerals provides a remarkably good opportunity for the Investigation of deep-seated rock constituents, for it is reasonable to suppose that these same elements are widely distributed in minute amounts through the parent rocks to which they are genetically related; but their concentration in pegmatite bodies affords a record of their presence that is lacking in other rocks. The unusual number of rare minerals of the Amelia, Virginia, pegmatites has long attracted attention, and the rare elements of the more abundant minerals which have been investigated in the laboratories of the United States Geological Survey afford an unusual opportunity to study the rare constituents of a pegmatite. This famous locality for rare minerals is situated 38 miles southwest of Richmond, just south of Appomattox River, on the Piedmont plateau.

Eos, Transactions, American Geophysical Union↗
USGS2024

Lead isotopes in New England (USA) volcanogenic massive sulphide deposits: Implications for metal sources and pre-accretionary tectonostratigraphic terranes

Lead isotope values for volcanogenic massive sulfide (VMS) deposits provide important insights into metal sources and the nature of pre-accretionary tectonostratigraphic terranes and underlying basements. Deposits of this type in New England formed in diverse tectonic settings including volcanic arcs and backarcs, a supra–subduction zone arc, a rifted forearc foreland basin, and a rifted continental margin. Following VMS mineralization on or near the seafloor, components of the tectonostratigraphic assemblages—volcanic ± sedimentary rocks, coeval intrusions, sulfide deposits, and underlying basements—were diachronously accreted to the Laurentian margin during the Paleozoic. Lead isotope data for galena show relatively large ranges for 206 Pb/ 204 Pb, 207 Pb/ 204 Pb, and 208 Pb/ 204 Pb. Evaluation of potential lead sources, using for comparison Pb-isotope data from modern and ancient settings, suggests that principal sources include the mantle, volcanic ± sedimentary rocks, and deeper basement rocks. Integration of the Pb-isotope values with published data such as Nd isotopes for the volcanic rocks and from deep seismic reflection profiles points to the involvement of several basements, including those of Grenvillian, Ganderian, Avalonian, and West African (and (or) Amazonian) affinity. Clustering of Pb-isotope data for VMS deposits within individual Cambrian and Ordovician volcanic and volcanosedimentary settings, delineated by differences in 206 Pb/ 204 Pb and µ ( 238 U/ 204 Pb) values, are consistent with lead derivation from at least four and possibly five different tectonostratigraphic assemblages with isotopically distinct basements. Collectively, our Pb-isotope data for New England VMS deposits provide a novel window into the nature of subarc basement rocks during pre-accretionary sulfide mineralization outboard of Laurentia during early Paleozoic time.

Canadian Journal of Earth Sciences↗
USGS2002

Argon thermochronology of mineral deposits; a review of analytical methods, formulations, and selected applications

40Ar/39Ar geochronology is an experimentally robust and versatile method for constraining time and temperature in geologic processes. The argon method is the most broadly applied in mineral-deposit studies. Standard analytical methods and formulations exist, making the fundamentals of the method well defined. A variety of graphical representations exist for evaluating argon data. A broad range of minerals found in mineral deposits, alteration zones, and host rocks commonly is analyzed to provide age, temporal duration, and thermal conditions for mineralization events and processes. All are discussed in this report. The usefulness of and evolution of the applicability of the method are demonstrated in studies of the Panasqueira, Portugal, tin-tungsten deposit; the Cornubian batholith and associated mineral deposits, southwest England; the Red Mountain intrusive system and associated Urad-Henderson molybdenum deposits; and the Eastern Goldfields Province, Western Australia.

Bulletin↗
USGS1982

Uranium and other element geochemical covariation in a granitic host rock and in the derived sediment, Deep Creek Range, Juab County, Utah

Correlation and factor analysis of geochemical data from a Tertiary biotite quartz monzonite, the Ibapah stock, and from derived sediment shows on comparison a major shift in element covariation among uranium and 24 other elements. Samples used were collected for a 1978 study in the central part of the Deep Creek Range, Juab County, Utah. Computed correlations among elements in granitic igneous rock samples suggest a high degree of covariation among elements that compose the rock. Uranium, however, shows significant correlation with only 12 elements and almost zero correlation with thorium. Computed correlations among elements in the derived sediment suggest that major decreases have occurred in covariation of the elements in the derived sands. Uranium in the sands, however, shows 15 significant correlations compared to 12 in the igneous rock samples, and shows an extremely high correlation with thorium. Factor analysis shows three geochemical petrogenic factors and the regional Be-U mineralization factor in the igneous rocks, and two mechanical segregation and one chemical precipitation factors in the sediments.

Open-File Report↗
USGS2004

Mineralogy at Meridiani Planum from the Mini-TES experiment on the opportunity rover

The Miniature Thermal Emission Spectrometer (Mini-TES) on Opportunity investigated the mineral abundances and compositions of outcrops, rocks, and soils at Meridiani Planum. Coarse crystalline hematite and olivine-rich basaltic sands were observed as predicted from orbital TES spectroscopy. Outcrops of aqueous origin are composed of 15 to 35% by volume magnesium and calcium sulfates [a high-silica component modeled as a combination of glass, feldspar, and sheet silicates (???20 to 30%)], and hematite; only minor jarosite is identified in Mini-TES spectra. Mini-TES spectra show only a hematite signature in the millimeter-sized spherules. Basaltic materials have more plagioclase than pyroxene, contain olivine, and are similar in inferred mineral composition to basalt mapped from orbit. Bounce rock is dominated by clinopyroxene and is close in inferred mineral composition to the basaltic martian meteorites. Bright wind streak material matches global dust. Waterlain rocks covered by unaltered basaltic sands suggest a change from an aqueous environment to one dominated by physical weathering.

Science↗
USGS2018

High microscale variability in Raman thermal maturity estimates from shale organic matter

Raman spectroscopy has recently received attention as a means to estimate thermal maturity of organic matter in petroleum generating source rocks to complement more traditional approaches such as vitrinite reflectance and programmed pyrolysis. While many studies have observed positive correlations between source rock thermal maturity and Raman spectral parameters, little attention has been given to the degree of variation in the Raman response across individual organic grains, especially for shales or mudrocks with highly dispersed organic matter. Here the spatial variation in Raman estimates of thermal maturity within individual organic grains is assessed from shales from the Boquillas, Marcellus, Niobrara, and Woodford Formations. The thermal maturity parameters extracted from Raman spectra can vary widely across distances of ≤5 μm within the same organic grain. These results illustrate the high degree of chemical heterogeneity inherent to the organic matter within these source rocks. Additionally, the spatial pattern of the Raman parameters, as revealed by 2D Raman mapping, imply that organic matter structure is influenced by associations with mineral surfaces within the surrounding rock matrix. Chemical heterogeneity and matrix effects directly impact the Raman response from these types of materials and thus the extracted thermal maturity estimate. These findings highlight the care which must be adopted when making Raman measurements of organic matter within source rock matrices, especially for samples which feature highly dispersed, heterogeneous organic matter as found in petroliferous mudrocks.

International Journal of Coal Geology↗
USGS2021

Brine-driven destruction of clay minerals in Gale crater, Mars

Mars’ sedimentary rock record preserves information on geological (and potential astrobiological) processes that occurred on the planet billions of years ago. The Curiosity rover is exploring the lower reaches of Mount Sharp, in Gale crater on Mars. A traverse from Vera Rubin ridge to Glen Torridon has allowed Curiosity to examine a lateral transect of rock strata laid down in a martian lake ~3.5 billion years ago. We report spatial differences in the mineralogy of time-equivalent sedimentary rocks <400 meters apart. These differences indicate localized infiltration of silica-poor brines, generated during deposition of overlying magnesium sulfate–bearing strata. We propose that destabilization of silicate minerals driven by silica-poor brines (rarely observed on Earth) was widespread on ancient Mars, because sulfate deposits are globally distributed.

Science↗
USGS1999

Age constraints on Jerritt Canyon and other Carlin-type gold deposits in the western United States-relationship to mid-Tertiary extension and magmatism

Carlin-type gold deposits are difficult to date and a wide range of ages has been reported for individual deposits. Therefore, several methods were employed to constrain the age of the gold deposits in the Jerritt Canyon district. Dated igneous rocks with well-documented crosscutting relationships to ore provided the most reliable constraints. K/Ar and 40 Ar/ 39 Ar dates on igneous rocks are as follows: andesite dikes 324 Ma, sericitic alteration in andesite dikes 118 Ma, basalt dikes 40.8 Ma, quartz monzonite dikes 39.2 Ma, and calc-alkaline ignimbrites 43.1 to 40.1 Ma. Of these, only the andesite and basalt dikes are clearly altered and mineralized. The gold deposits are, therefore, younger than the 40.8 Ma basalt dikes. The sericitic alteration in the andesite dikes is unrelated to the gold deposits. A number of dating techniques did not work. K/Ar and 40 Ar/ 39 Ar dates on mica from mineralized Ordovician to Devonian sedimentary rocks gave misleading results. The youngest date of 149 Ma from the smallest <0.1-mu m-size fraction shows that the temperature (120 degrees -260 degrees C) and duration (?) of hydrothermal activity was insufficient to reset preexisting fine-grained micas in the host rocks. The temperature and duration was also insufficient to anneal fission tracks in zircon from Ordovician quartzites as they yield Middle Proterozoic dates in both mineralized and barren samples. Apatites were too small for fission track dating. Hydrothermal sulfides have pronounced crustal osmium isotope signatures ( 187 Os/ 188 Os initial = 0.9-3.6) but did not yield a meaningful isochron due to very low Re and Os concentrations and large analytical uncertainties. Paleomagnetic dating techniques failed because the hydrothermal fluids sulfidized nearly all of the iron in the host rocks leaving no remnant magnetism.When published isotopic dates from other Carlin-type deposits in Nevada and Utah are subject to the rigorous evaluation developed for the Jerritt Canyon study, most deposits can be shown to have formed between 42 and 30 Ma. K/Ar and 40 Ar/ 39 Ar dates on the youngest preore igneous rocks range from 41 to 32 Ma, whereas the oldest postore igneous rocks range from 35 to 33 Ma. Hydrothermal adularia from the Twin Creeks deposit yields similar 40 Ar/ 39 Ar dates of 42 Ma. K/Ar dates on supergene alunite range from 4 to 30 Ma. K/Ar and 40 Ar/ 39 Ar dates on micas separated from sedimentary (395-43 Ma) and igneous (145-38 Ma) rocks are usually much older than the gold deposits and most are suspect because they are from incompletely reset preore micas or from mixtures of preore and ore-stage mica. Fission track dates on zircons are also generally older than the deposits (169-35 Ma) and are not completely reset by mineralization. Apatites are likley to be reset by the hydrothermal systems (and by younger thermal events) and yield dates (83-22 Ma) that are younger than those from zircon. Independent support of a mid-Tertiary age is provided by the low delta D (sub H 2 O) values of hydrothermal fluids from 10 widely separated Carlin-type deposits (-134 + or - 23ppm). The low delta D (sub H 2 O) values are consistent with a mid-Tertiary age when the climate was cool but are inconsistent with the Cretaceous and Jurassic ages favored by some workers when the climate was warm. The age and distribution of Carlin-type deposits coincides with areas that underwent extension and calc-alkaline magmatism over the same time period. Despite this relationship, the deposits lack clear spatial or genetic relationships to mid-Tertiary epizonal plutons. Rather, many deposits are localized along preexisting crustal fault zones. In the Getchell trend, structures tapped deep-sourced metamorphic (or magmatic) fluids and subsequently variably exchanged meteoric water. In the other trends and districts only variably exchanged meteoric water has been detected. These relationships suggest either that all of the deposits formed from deep-sourced fluids and were subsequently flooded by meteoric water, or, that fluids from different sources evolved to produce deposits with similar charateristics.

Economic Geology↗
USGS2012

Tectonic relations of carbon dioxide discharges and earthquakes

CO 2 ‐rich springs occur worldwide along major zones of seismicity. They are mostly in young orogenic belts, but some are in areas of rifting continental platforms. Analyses of 13 C content indicate that much of the CO 2 is derived from the mantle and that other important sources are the metamorphism of marine carbonate‐bearing sedimentary rocks and the degradation of organic material. The presence of calc‐silicate minerals, such as pumpellyite in metagraywacke, is evidence of former conversion of carbonate‐bearing rocks into calc‐silicate minerals and release of CO 2 . The CO 2 pressure in fractured rocks of a fault zone reduces the effective normal stress and, if it is sufficiently great, allows the fault to slip. If the pressure were maintained at a sufficiently high level, the fault behavior might be characterized by frequent small earthquakes and aseismic creep such as occur along active segments of the San Andreas system. The presence of CO 2 ‐rich springs may indicate a potentially hazardous seismic region. Monitoring of CO 2 discharges could be useful in earthquake prediction.

Journal of Geophysical Research B: Solid Earth↗
USGS1963

Fluvial sediments a summary of source, transportation, deposition, and measurement of sediment discharge

This paper presents a broad but undetailed picture of fluvial sediments in streams, reservoirs, and lakes and includes a discussion of the processes involved in the movement of sediment by flowing water. Sediment is fragmental material that originates from the chemical or physical disintegration of rocks. The disintegration products may have many different shapes and may range in size from large boulders to colloidal particles. In general, they retain about the same mineral composition as the parent rocks. Rock fragments become fluvial sediment when they are entrained in a stream of water. The entrainment may occur as sheet erosion from land surfaces, particularly for the fine particles, or as channel erosion after the surface runoff has accumulated in streams. Fluvial sediments move in streams as bedload (particles moving within a few particle diameters of the streambed) or as suspended sediment in the turbulent flow. The discharge of bedload varies with several factors, which may include particle size and a type of effective shear on the surface of the streambed. The discharge of suspended sediment depends partly on concentration of moving sediment near the streambed and hence on discharge of bedload. However, the concentration of fine sediment near the streambed varies widely, even for equal flows, and, therefore, the discharge of fine sediment normally cannot be computed theoretically. The discharge of suspended sediment also depends on velocity, turbulence, depth of flow, and fall velocity of the particles. In general, the coarse sediment transported by a stream moves intermittently and is discharged at a rate that depends on properties of the flow and of the sediment. If an ample supply of coarse sediment is available at the surface of the streambed, the discharge of the coarse sediment, such as sand, can be roughly computed from properties of the available sediment and of the flow. On the other hand, much of the fine sediment in a stream usually moves nearly continuously at about the velocity of the flow, and even low flows can transport large amounts of fine sediment. Hence, the discharge of fine sediments, being largely dependent on the availability of fine sediment upstream rather than on the properties of the sediment and of the flow at a cross section, can seldom be computed from properties, other than concentrations based directly on samples, that can be observed at the cross section. Sediment particles continually change their positions in the flow; some fall to the streambed, and others are removed from the bed. Sediment deposits form locally or over large areas if the volume rate at which particles settle to the bed exceeds the volume rate at which particles are removed from the bed. In general, large particles are deposited more readily than small particles, whether the point of deposition is behind a rock, on a flood plain, within a stream channel, or at the entrance to a reservoir, a lake, or the ocean. Most samplers used for sediment observations collect a water-sediment mixture from the water surface to within a few tenths of a foot of the streambed. They thus sample most of the suspended sediment, especially if the flow is deep or if the sediment is mostly fine; but they exclude the bedload and some of the suspended sediment in a layer near the streambed where the suspended-sediment concentrations are highest. Measured sediment discharges are usually based on concentrations that are averages of several individual sediment samples for a cross section. If enough average concentrations for a cross section have been determined, the measured sediment discharge can be computed by interpolating sediment concentrations between sampling times. If only occasional samples were collected, an average relation between sediment discharge and flow can be used with a flow-duration curve to compute roughly the average or the total sediment discharges for any periods of time for which the flow-duration c

Bulletin↗
USGS2012

Nickel: makes stainless steel strong

Nickel is a silvery-white metal that is used mainly to make stainless steel and other alloys stronger and better able to withstand extreme temperatures and corrosive environments. Nickel was first identified as a unique element in 1751 by Baron Axel Fredrik Cronstedt, a Swedish mineralogist and chemist. He originally called the element kupfernickel because it was found in rock that looked like copper ( kupfer ) ore and because miners thought that "bad spirits" ( nickel ) in the rock were making it difficult for them to extract copper from it. Approximately 80 percent of the primary (not recycled) nickel consumed in the United States in 2011 was used in alloys, such as stainless steel and superalloys. Because nickel increases an alloy's resistance to corrosion and its ability to withstand extreme temperatures, equipment and parts made of nickel-bearing alloys are often used in harsh environments, such as those in chemical plants, petroleum refineries, jet engines, power generation facilities, and offshore installations. Medical equipment, cookware, and cutlery are often made of stainless steel because it is easy to clean and sterilize. All U.S. circulating coins except the penny are made of alloys that contain nickel. Nickel alloys are increasingly being used in making rechargeable batteries for portable computers, power tools, and hybrid and electric vehicles. Nickel is also plated onto such items as bathroom fixtures to reduce corrosion and provide an attractive finish.

Fact Sheet↗
USGS1985

Map showing geochemical summary for the Bald Rock and Middle Fork Feather River Roadless Areas, Butte and Plumas counties, California

The Bald Rock Roadless Area consists of 3,850 acres in Butte County, Calif. The Middle Rock Feather River Roadless Area consists of 29,300 acres ub Butte and Plumas Counties, Calif. Both roadless areas are in the Plumas National Forest and are on the west slope of the northern Sierra Nevada southwest of Quincy, Calif. (fig. 1). The two roadless areas are alined along the Middle Fork of the Feather River where they include the narrow canyon bottoms and precipitous sidewalls of the Middle Fork and several tributary drainages. Altitudes range from 800 ft in the canyon of the Middle Fork to approximately 6,600 ft at the northwest corner of the map area. The geology of the roadless areas has been briefly summarized by Sorenson and Pietropaoll (1982). This paper summarizes and interprets the semiquantitative emission spectrographic analyses of 106 rock sample and 165 samples of nonmagnetics heavy-mineral stream-sediment concentrates from the Blad Rock and Middle Fork Feather River Roadless Area (Sorenson and others, 1982).

California↗
USGS2000

Diagenesis of the Purington Shale in the Illinois Basin and implications for the diagenetic state of sedimentary rocks of shallow Paleozoic basins

The clay minerals, micas, and feldspars of the Pennsylvanian-age Purington Shale have been more diagenetically active than generally recognized. They have undergone diagenetic changes comparable to those of Cenozoic and Mesozoic sedimentary rocks buried three to four times as deeply and heated to approximately twice the temperature. The Purington Shale on the Western Shelf of the Illinois Basin has experienced maximum burial of ???1.0 km and was never heated to more than 60??C, except for a very brief time at about 80??C. The illite/smectite (I/S) of the Purington Shale has ???90% illite. The chemical compositions of the feldspar assemblage in the 0.09-0.063-mm fraction differ from most modern detrital suites of feldspars but are similar to diagenetic sequences described by others from much greater burial depths and are extensively, but not completely, albitized. The simplest interpretation of the apparently advanced stage of diagenesis is that the diagenetic processes have been operating at less pressure and lower temperature but for a longer time; an example of low-temperature, time-dependent diagenesis. By similar reasoning, the apparently anomalously advanced maturity of all of the sedimentary rocks in the relatively shallow Illinois Basin is explained. This generalization should be considered for all shallow Paleozoic basins and should influence (1) exploration for petroleum, (2) use of modal and chemical analyses for determining provenance, and (3) use of chemical composition of shales as proxy for crustal evolution.

Journal of Geology↗
USGS1987

Evidence for Late-Paleozoic brine migration in Cambrian carbonate rocks of the central and southern Appalachians: Implications for Mississippi Valley-type sulfide mineralization

Many Lower Paleozoic limestones and dolostones in the Valley and Ridge province of the central and southern Appalachians contain 10 to 25 weight percent authigenic potassium feldspar. This was considered to be a product of early diagenesis, however, 40 Ar 39 Ar "> 40 Ar 39 Ar analyses of overgrowths on detrital K-feldspar in Cambrian carbonate rocks from Pennsylvania, Maryland, Virginia, and Tennessee yield Late Carboniferous-Early Permian ages (278–322 Ma). Simple mass balance calculations suggest that the feldspar could not have formed isochemically, but required the flux of multiple pore volumes of fluid through the rocks, reflecting regional fluid migration events during the Late-Paleozoic Alleghanian orogeny. Microthermometric measurements of fluid inclusions in overgrowths on detrital K-feldspar and quartz grains from unmineralized rocks throughout the study area indicate homogenization temperatures from 100° to 200°C and freezing point depressions of −14° to −18.5°C (18–21 wt.% NaCl equiv). The apparent similarity of these fluids to fluid inclusions in ore and gangue minerals of nearby Mississippi Valley-type (MVT) deposits suggests that the regional occurrences of authigenic K-feldspar and MVT mineralization may be genetically related. This hypothesis is supported by the discovery of authigenic K-feldspar intergrown with sphalerite in several mines of the Mascot-Jefferson City District, E. Tennessee. Regional potassic alteration in unmineralized carbonate rocks and localized occurrences of MVT mineralization are both explainable by a gravity-driven flow model, in which deep brines migrate towards the basin margin under a hydraulic gradient established during the Alleghanian orogeny. The authigenic K-feldspar may reflect the loss of K during disequilibrium cooling of the ascending brines. MVT deposits are probably localized manifestations of the same migrating fluids, occurring where the necessary physical and chemical traps are present.

Geochimica et Cosmochimica Acta↗
USGS2021

Hydrogeochemistry in the Yukon-Tanana Upland region of east-central Alaska: Possible exploration tool for porphyry-style deposits

A hydrogeochemical study using high resolution ICP-MS was undertaken at the Taurus and other porphyry Cu-Mo(-Au) occurrences and Ag-Au-Cu (+/- Pb, Zn) occurrences with epithermal-style characteristics in the Yukon-Tanana upland region of eastern Alaska. Surface water samples were collected from 30 sites on creeks that drain known deposits and occurrences and surrounding presumably unmineralized areas. Water samples for the entire ∼9 km length of McCord Creek, which drains the Taurus deposit, and those from streams draining the areas at and near the Bluff and Dennison porphyry occurrences have high conductivity values (492 to 1250 μS/cm) and consistently high concentrations of B (3-250 μg/L), Co (2.3 to 42 μg/L), Mn (339 to 4750 μg/L), Re (0.012 to 0.1 μg/L), and SO 4 2- (>200 mg/L), all of which are well above the median value for this data set and significantly greater than concentrations in water samples from the unmineralized areas. These are the best pathfinder elements specifically for porphyry style deposits because most of them are not anomalous in waters near epithermal occurrences. Copper concentrations are high (up to 115 μg/L) in some low-pH water samples from McCord Creek and drainages around Bluff, and a few near neutral pH waters have high molybdenum (>1 μg/L), but neither element is consistently anomalous in close vicinity to the porphyry occurrences, possibly due to a metal-poor, sulfide-poor leached cap (average of ∼50 m) that overlies supergene and hypogene mineralized zones and is the dominant rock at surface. High concentrations of Bi and/or As occur in many waters associated with mineralized areas, particularly the Bluff and Dennison occurrences. In general, the element associations related to porphyry deposits reflect the deposit mineralogy, as well as size of the footprint related to alteration and mineralization.

Alaska↗
USGS1963

Degree of oxidation of adirondack iron oxide and iron-titanium oxide minerals in relation to petrogeny

Partial chemical analyses of the accessory iron oxide and iron-titanium oxide minerals from more than one hundred samples of Adirondack igneous, metamorphic, and metasomatic rocks portray the degree of oxidation of the minerals and afford a basis for a discussion of their relation to the accompanying silicate assemblage and petrogeny. Among the granitic igneous rocks, the green pyroxenic facies have the least oxidized iron-titanium oxide minerals and a pink potassium-rich microperthitic microcline facies the most oxidized. Granites and syenites may crystallize with either an iron-rich variety of hornblende (or pyroxene) plus ilmenite, or with an iron-magnesium variety of hornblende (or of pyroxene) plus magnetite plus ilmenite, depending on the degree of oxidation. The granite facies of the orthogneisses of the Diana Complex (Precambrian) have a more oxidized mineral assemblage than the syenitic and quartz syenitic facies. The anorthosites and gabbro anorthosites have relatively oxygen-rich oxide minerals. Orthogneisses in the granulite facies have a lower ratio of Fe 2 O 3 /FeO than similar gneisses in the amphibolite facies. At least part of this lower ratio is due to metamorphism at higher temperatures and pressures. A regional belt of granitic orthogneiss metamorphosed in the amphibolite facies has a magnetite-sphene instead of a magnetite-ilmenite assemblage. Metasomatism of biotite-quartz-plagioclase gneiss to sillimanitic quartz-microcline gneisses is accompanied by decrease in mafic silicates and a series of changes of minerals in intermediate stages such that, in general, biotite yields with increasing degrees of oxidation successively such assemblages as (1) biotite, garnet, magnetite, hemo-ilmenite, and ilmeno-hematite; (2) pale brown mica, sillimanite, magnetite, and ilmeno-hematite; and (3) rutilo-hematite, rutile, and meagre silicates including sillimanite, muscovite, and chlorite. Diabase altered to monzodiorite by potassium-bearing solutions has ilmeno-magnetite partly altered to ilmeno-maghemite.

Journal of Petrology↗
USGS1963

Geology of the Anlauf and Drain quadrangles, Douglas and Lane counties, Oregon

The Anlauf and Drain quadrangles, Oregon, lie about 20 miles south of the City of Eugene, in Douglas and Lane Counties. They constitute an area of about 435 square miles that includes parts of both the Cascade Range and Coast Range physiographic provinces. A sequence of lower Tertiary sedimentary and volcanic rocks with a maximum thickness of about 20,000 feet is exposed in the area. The oldest part of this sequence is the Umpqua formation of early Eocene age consisting of a lower Member of vesicular and amygdaloidal olivine basalt flows, a middle member of water-laid vitric and lapilli crystal tuff, and an upper member of interbedded fissile siltstone and basaltic sandstone which contains a 300-foot tongue of massive to thick-bedded basaltic sandstone near its top. These rocks are predominantly of marine origin, although the general absence of pillow structures Which are common in basaltic lavas of equivalent age elsewhere in the Coast Ranges suggests that some of the flows were poured out subaerially. The overlying tuff member, however, contains Foraminifera and in places has a lime content slightly in excess of 10 percent. Mollusca and Foraminifera indicate that the Umpqua formation is of early Eocene age and is a correlative of the Capay formation of California. The Tyee formation of middle Eocene age overlies the Umpqua formation and consists of more than 5,000 feet of rhythmically deposited sandstone and siltstone in beds 2 to 30 feet thick. The basal part of each bed consists of medium- to coarse-grained sandstone that grades upward into line-grained sandstone and siltstone. The principal constituents of the sandstone are quartz, partly altered feldspar, mica, clay, and fragments of basalt, fine-grained argillaceous rocks, and mica schist. Other detrital minerals include epidote, garnet, blue-green hornblende, tourmaline, and zoisite. The depositional environment of the Tyee formation is poorly known, although the rhythmic-graded bedding suggests turbidity currents. About 500 feet of sandstone and siltstone assigned to the Spencer formation of late Eocene age unconformably overlies the Tyee formation. The Spencer formation, better exposed in the east-central part of the Coast Ranges, contains marine fossils but also has thin impure coal beds, indicative of strand-line accumulation. The sandstone in the Spencer formation is very similar to that in the Tyee formation, from which it was probably derived. The Fisher formation contains about 5,500 feet of nonmarine pyroclastic and Volcanic rocks that are related to the volcanic rock sequences of the western Cascade Range. The formation is characterized by a wide variety of rock types, including conglomerate, tuffaceous sandstone and siltstone, vitric and crystal tuff, waterlaid and mudflow breccia, and andesitic lava flows. These rocks generally occur in lenticular beds that have little stratigraphic significance. The rocks apparently accumulated on a plain slightly above sea level that was subjected alternately to flooding by running water and to desiccation. Fossil leaves from the lowermost part of the Fisher formation are of late Eocene age; the upper part of the formation is of early, and possibly middle, Oligocene age. A few exposures of olivine basalt were mapped in the extreme northern part of the Anlauf quadrangle. The flows, more extensively exposed to the north, overlie the Fisher formation, and, therefore, are tentatively considered to be post-Oligocene in age. All these stratigraphic units, but principally the Fisher formation, are cut by dikes, sills, and stocklike bodies of porphyritic basalt, diabase, and norite. Contemporaneously with the emplacement of most of these rocks, in late Miocene(?) time, hydrothermal solutions locally altered the sedimentary and extrusive igneous rocks and deposited cinnabar and other sulfide minerals, carbonates, and silica. Three parallel northeastward-trending anticlines in the older marine rocks are the most conspicuous structural features in the area. These folds plunge both to the northeast and southwest and expose in their central parts basalt flows of the Umpqua formation. The rocks along the west margin of the area dip westward into a structural basin in the adjacent Elkton quadrangle, whereas to the east the Fisher formation generally has an easterly dip typical of the nonmarine rocks in the western Cascade Range. Geologic studies in the Anlauf and Drain quadrangles were undertaken principally to evaluate the petroleum possibilities of the area. Available data indicate that source beds and reservoir rock suitable for the formation and accumulation of petroleum are absent in this part of the Coast Ranges, but because of the lack of subsurface information, this evaluation is only tentative. Mineral deposits of economic value in the area include quicksilver and alumina clay.

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