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At least 559 records · Page 31Linked to original sources
USGS1983

Mapping of hydrothermally altered rocks using airborne multispectral scanner data, Marysvale, Utah, mining district

Multispectral data covering an area near Marysvale, Utah, collected with the airborne National Aeronautics and Space Administration (NASA) 24-channel Bendix multispectral scanner, were analyzed to detect areas of hydrothermally altered, potentially mineralized rocks. Spectral bands were selected for analysis that approximate those of the Landsat 4 Thematic Mapper and which are diagnostic of the presence of hydrothermally derived products. Hydrothermally altered rocks, particularly volcanic rocks affected by solutions rich in sulfuric acid, are commonly characterized by concentrations of argillic minerals such as alunite and kaolinite. These minerals are important for identifying hydrothermally altered rocks in multispectral images because they have intense absorption bands centered near a wavelength of 2.2 ??m. Unaltered volcanic rocks commonly do not contain these minerals and hence do not have the absorption bands. A color-composite image was constructed using the following spectral band ratios: 1.6??m/2.2??m, 1.6??m/0.48??m, and 0.67??m/1.0??m. The particular bands were chosen to emphasize the spectral contrasts that exist for argillic versus non-argillic rocks, limonitic versus nonlimonitic rocks, and rocks versus vegetation, respectively. The color-ratio composite successfully distinguished most types of altered rocks from unaltered rocks. Some previously unrecognized areas of hydrothermal alteration were mapped. The altered rocks included those having high alunite and/or kaolinite content, siliceous rocks containing some kaolinite, and ash-fall tuffs containing zeolitic minerals. The color-ratio-composite image allowed further division of these rocks into limonitic and nonlimonitic phases. The image did not allow separation of highly siliceous or hematitically altered rocks containing no clays or alunite from unaltered rocks. A color-coded density slice image of the 1.6??m/2.2??m band ratio allowed further discrimination among the altered units. Areas containing zeolites and some ash-fall tuffs containing montmorillonite were readily recognized on the color-coded density slice as having less intense 2.2-??m absorption than areas of highly altered rocks. The areas of most intense absorption, as depicted in the color-coded density slice, are dominated by highly altered rocks containing large amounts of alunite and kaolinite. These areas form an annulus, approximately 10 km in diameter, which surrounds a quartz monzonite intrusive body of Miocene age. The patterns of most intense alteration are interpreted as the remnants of paleohydrothermal convective cells set into motion during the emplacement of the central intrusive body. ?? 1983.

Advances in Space Research↗
USGS1957

Core logs from Owens, China, Searles, and Panamint basins, California

Detailed logs of drill cores are presented in this report. The drill cores are of sediments from four basins that were occupied during the Pleistocene by a continuous chain of lakes. Owens Lake basin (one hole, 920 feet) contains fine-grained sediments and includes locally many diatoms and ostracodes. China Lake basin (one hole, 700 feet) contains silt- to sand-sized clastic sediments and some calcite and gaylussite; a few diatoms, ostracodes, and mollusks are present. Searles Lake basin (one hole, 875 feet) contains many layers of gaylussite- or pirssonite-bearing sediments intercalated with beds of halite, trona, and lesser amounts of other minerals peculiar to Searles Lake; the top 120 feet consists of thicker evaporite bodies with a more complex mineralogy. Panamint basin (three holes, 500, 375, and 995 feet) contains clastic deposits ranging from clay to gravel, a small amount of gypsum, anhydrite, a trace of bassanite, and thick bodies of halite in the basin center; a few diatoms and ostracodes are present.

Bulletin↗
USGS1987

Dinosaurs, spherules, and the “magic” layer: A new K-T boundary clay site in Wyoming

A new Cretaceous-Tertiary (K-T) boundary clay site has been found along Dogie Creek in Wyoming in the drainage of Lance Creek—the type area of the Lance Formation of latest Cretaceous age. The boundary clay was discovered in the uppermost part of the Lance Formation, 4–7 cm beneath the lowest lignite in the Paleocene Fort Union Formation and approximately 1 m above a fragmented dinosaur bone. The boundary clay consists of a basal kaolinitic claystone layer as much as 3 cm thick containing hollow goyazite spherules, overlain by a 2–3 mm smectitic layer (the “magic” layer) containing both shock-metamorphosed minerals and an iridium anomaly of 21 ppb. A palynological break coincides with the base of the claystone layer; numerous Late Cretaceous palynomorph species terminate at this boundary. The paleontological significance of this new boundary site lies in its close association with the well-studied assemblage of dinosaurs and other vertebrates and flora within the type area of the Lance Formation. The spherules at the Dogie Creek site are extremely well preserved by virtue of their replacement by the mineral goyazite. This preservation should facilitate the resolution of the origin of the spherules and of their host layer.

Wyoming↗
USGS2008

Deposition of talc - kerolite-smectite - smectite at seafloor hydrothermal vent fields: Evidence from mineralogical, geochemical and oxygen isotope studies

Talc, kerolite-smectite, smectite, chlorite-smectite and chlorite samples from sediments, chimneys and massive sulfides from six seafloor hydrothermal areas have been analyzed for mineralogy, chemistry and oxygen isotopes. Samples are from both peridotite- and basalt-hosted hydrothermal systems, and basaltic systems include sediment-free and sediment-covered sites. Mg-phyllosilicates at seafloor hydrothermal sites have previously been described as talc, stevensite or saponite. In contrast, new data show tri-octahedral Mg-phyllosilicates ranging from pure talc and Fe-rich talc, through kerolite-rich kerolite-smectite to smectite-rich kerolite-smectite and tri-octahedral smectite. The most common occurrence is mixed-layer kerolite-smectite, which shows an almost complete interstratification series with 5 to 85% smectitic layers. The smectite interstratified with kerolite is mostly tri-octahedral. The degree of crystal perfection of the clay sequence decreases generally from talc to kerolite-smectite with lower crystalline perfection as the proportion of smectite layers in kerolite-smectite increases. Our studies do not support any dependence of the precipitated minerals on the type/subtype of hydrothermal system. Oxygen isotope geothermometry demonstrates that talc and kerolite-smectite precipitated in chimneys, massive sulfide mounds, at the sediment surface and in open cracks in the sediment near seafloor are high-temperature (> 250????C) phases that are most probably the result of focused fluid discharge. The other end-member of this tri-octahedral Mg-phyllosilicate sequence, smectite, is a moderate-temperature (200-250????C) phase forming deep within the sediment (??? 0.8??m). Chlorite and chlorite-smectite, which constitute the alteration sediment matrix around the hydrothermal mounds, are lower-temperature (150-200????C) phases produced by diffuse fluid discharge through the sediment around the hydrothermal conduits. In addition to temperature, other two controls on the precipitation of this sequence are the silica activity and Mg/Al ratio (i.e. the degree of mixing of seawater with hydrothermal fluid). Higher silica activity favors the formation of talc relative to tri-octahedral smectite. Vent structures and sedimentary cover preclude complete mixing of hydrothermal fluid and ambient seawater, resulting in lower Mg/Al ratios in the interior parts of the chimneys and deeper in the sediment which leads to the precipitation of phyllosilicates with lower Mg contents. Talc and kerolite-smectite have very low trace- and rare earth element contents. Some exhibit a negative or flat Eu anomaly, which suggests Eu depletion in the original hydrothermal fluid. Such Eu depletion could be caused by precipitation of anhydrite or barite (sinks for Eu2+) deeper in the system. REE abundances and distribution patterns indicate that chlorite and chlorite-smectite are hydrothermal alteration products of the background turbiditic sediment. ?? 2007 Elsevier B.V. All rights reserved.

Chemical Geology↗
USGS1998

Ordovician K-bentonites in the Argentine Precordillera: Relations to Gondwana margin evolution

Ordovician K-bentonites have now been recorded from >20 localities in the vicinity of the Argentine Precordillera. Most occur in the eastern thrust belts, in the San Juan Limestone and the overlying the Gualcamayo Formation, but a few ash beds are known also from the central thrust belts. The oldest occur in the middle Arenig I. victoriae lunatus graptolite ( Oe. evae conodont) Zone, and the youngest in the middle Llanvirn P. elegans ( P. suecicus ) Zone. Mineralogical characteristics, typical of other Ordovician K-bentonites, include a matrix of illite/smectite mixed-layer clay and a typical felsic volcanic phenocryst assemblage: biotite, beta-form quartz, alkali and plagioclase feldspar, apatite, and zircon, with lesser amounts of hornblende, clinopyroxene, titanite and Fe-Ti oxides. The proportions of the mineral phases and variations in their crystal chemistry are commonly unique to individual (or small groups of) K-bentonite beds. Glass melt inclusions preserved in quartz are rhyolitic in composition. The sequence is unique in its abundance of K-bentonite beds, but a close association between the Precordillera and other Ordovician sedimentary basins cannot be established. The ash distribution is most consistent with palaeogeographical reconstructions in which early Ordovician drifting of the Precordillera occurred in proximity to one or more volcanic arcs, and with eventual collision along the Andean margin of Gondwana during the mid-Ordovician Ocloyic event of the Famatinian orogeny. The Puna-Famatina terrane northeast of the Precordillera might have served as the source of the K-bentonite ashes, possibly in concert with active arc magmatism on the Gondwana plate itself.

Geological Society Special Publication↗
USGS2006

Environmental aspects of produced-water salt releases in onshore and coastal petroleum-producing areas of the conterminous U.S. - a bibliography

Environmental effects associated with the production of oil and gas have been reported since the first oil wells were drilled in the Appalachian Basin in Pennsylvania and Kentucky in the early to mid-1800s. The most significant of these effects are the degradation of soils, ground water, surface water, and ecosystems they support by releases of suspended and dissolved hydrocarbons and co-produced saline water. Produced water salts are less likely than hydrocarbons to be adsorbed by mineral phases in the soil and sediment and are not subject to degradation by biologic processes. Sodium is a major dissolved constituent in most produced waters and it causes substantial degradation of soils through altering of clays and soil textures and subsequent erosion. Produced water salts seem to have the most wide-ranging effects on soils, water quality, and ecosystems. Trace elements, including boron, lithium, bromine, fluorine, and radium, also occur in elevated concentrations in some produced waters. Many trace elements are phytotoxic and are adsorbed and may remain in soils after the saline water has been flushed away. Radium-bearing scale and sludge found in oilfield equipment and discarded on soils pose additional hazards to human health and ecosystems. This bibliography includes studies from across the oil- and natural-gas-producing areas of the conterminous United States that were published in the last 80 yrs. The studies describe the effects of produced water salts on soils, water quality, and ecosystems. Also included are reports that describe (1) the inorganic chemistry of produced waters included in studies of formation waters for various purposes, (2) other sources of salt affecting water quality that may be mistaken for produced water effects, (3) geochemical and geophysical techniques that allow discrimination of salt sources, (4) remediation technologies designed to repair damage caused to soils and ground water by produced water salts, and (5) contamination by naturally occurring radioactive materials (NORM)at oilfield sites.

Open-File Report↗
USGS2010

Mineral resource of the month: perlite

The article talks about perlite, which is a mineral used as an aggregate for lightweight construction products, filler for paints and horticultural soil blends. Perlite comes from viscous lava, mined and processed to produce lightweight material that competes with pumice, exfoliated vermiculite and expanded clay and shale. It is mined in about 35 countries that include Greece, Japan and the U.S. Other uses include insulation, concrete and plaster aggregate, and stonewashing.

Earth↗
USGS1990

A geochemical sampling technique for use in areas of active alpine glaciation: an application from the central Alaska Range

In mountainous regions containing extensive glacier systems there is a lack of suitable material for conventional geochemical sampling. As a result, in most geochemical sampling programs a few stream-sediment samples collected at, or near, the terminus of valley glaciers are used to evaluate the mineral potential of the glaciated area. We have developed and tested a technique which utilizes the medial moraines of valley glaciers for systematic geochemical exploration of the glacial catchment area. Moraine sampling provides geochemical information that is site-specific in that geochemical anomalies can be traced directly up-ice to bedrock sources. Traverses were made across the Trident and Susitna glaciers in the central Alaska Range where fine-grained (clay to sand size) samples were collected from each medial moraine. These samples were prepared and chemically analyzed to determine the concentration of specific elements. Fifty pebbles were collected at each moraine for archival purposes and for subsequent lithologic identification. Additionally, fifty cobbles and fifty boulders were examined and described at each sample site to determine the nature and abundance of lithologies present in the catchment area, the extent and nature of visible mineralization, the presence and intensity of hydrothermal alteration and the existence of veins, dikes and other minor structural features. Results from the central Alaska Range have delineated four distinct multi-element anomalies which are a response to potential mineralization up-ice from the medial moraine traverse. By integrating the lithologic, mineralogical and geochemical data the probable geological setting of the geochemical anomalies is determined.

Journal of Geochemical Exploration↗
USGS2006

Unusual Holocene and late Pleistocene carbonate sedimentation in Bear Lake, Utah and Idaho, USA

Bear Lake (Utah-Idaho, USA) has been producing large quantities of carbonate minerals of varying mineralogy for the past 17,000 years. The history of sedimentation in Bear Lake is documented through the study of isotopic ratios of oxygen, carbon, and strontium, percent organic carbon, percent CaCO3, X-ray diffraction mineralogy, HCl-leach inorganic geochemistry, and magnetic properties on samples from three piston cores. Historically, the Bear River, the main source of water for Great Salt Lake, did not enter Bear Lake until it was artificially diverted into the lake at the beginning of the 20th century. However, during the last glacial interval, the Bear River did enter Bear Lake depositing red, calcareous, silty clay. About 18,000 years ago, the Bear River became disconnected from Bear Lake. A combination of warmer water, increased evaporation, and increased organic productivity triggered the precipitation of calcium carbonate, first as calcite. As the salinity of the lake increased due to evaporation, aragonite began to precipitate about 11,000 years ago. Aragonite is the dominant mineral that accumulated in bottom sediments of the lake during the Holocene, comprising an average of about 70 wt.% of the sediments. Aragonite formation in a large, cold, oligotrophic, high latitude lake is highly unusual. Lacustrine aragonite usually is found in small, saline lakes in which the salinity varies considerably over time. However, Bear Lake contains endemic ostracodes and fish, which indicate that the chemistry of the lake has remained fairly constant for a long time. Stable isotope data from Holocene aragonite show that the salinity of Bear Lake increased throughout the Holocene, but never reached highly evolved values of ??18O in spite of an evaporation-dominated water balance. Bear Lake hydrology combined with evaporation created an unusual situation that produced large amounts of aragonite, but no evaporite minerals.

Sedimentary Geology↗
USGS2012

The impact of biotic/abiotic interfaces in mineral nutrient cycling: A study of soils of the Santa Cruz chronosequence, California

Biotic/abiotic interactions between soil mineral nutrients and annual grassland vegetation are characterized for five soils in a marine terrace chronosequence near Santa Cruz, California. A Mediterranean climate, with wet winters and dry summers, controls the annual cycle of plant growth and litter decomposition, resulting in net above-ground productivities of 280–600 g m −2 yr −1 . The biotic/abiotic (A/B) interface separates seasonally reversible nutrient gradients, reflecting biological cycling in the shallower soils, from downward chemical weathering gradients in the deeper soils. The A/B interface is pedologically defined by argillic clay horizons centered at soil depths of about one meter which intensify with soil age. Below these horizons, elevated solute Na/Ca, Mg/Ca and Sr/Ca ratios reflect plagioclase and smectite weathering along pore water flow paths. Above the A/B interface, lower cation ratios denote temporal variability due to seasonal plant nutrient uptake and litter leaching. Potassium and Ca exhibit no seasonal variability beneath the A/B interface, indicating closed nutrient cycling within the root zone, whereas Mg variability below the A/B interface denotes downward leakage resulting from higher inputs of marine aerosols and lower plant nutrient requirements. The fraction of a mineral nutrient annually cycled through the plants, compared to that lost from pore water discharge, is defined their respective fluxes F j,plants = q j,plants /( q j,plants + q j,discharge ) with average values for K and Ca ( F K,plants = 0.99; F Ca,plants = 0.93) much higher than for Mg and Na ( F Mg,plants 0.64; F Na,plants = 0.28). The discrimination against Rb and Sr by plants is described by fractionation factors ( K Sr/Ca = 0.86; K Rb/K = 0.83) which are used in Rayleigh fractionation-mixing calculations to fit seasonal patterns in solute K and Ca cycling. K Rb/K and K 24 Mg / 22 Mg "> K24Mg/22Mg values (derived from isotope data in the literature) fall within fractionation envelopes bounded by inputs from rainfall and mineral weathering. K Sr/Ca and K 44 Ca / 40 Ca "> K44Ca/40Ca fractionation factors fall outside these envelopes indicating that Ca nutrient cycling is closed to these external inputs. Small net positive K and Ca fluxes (6–14 mol m −2 yr −1 ), based on annual mass balances, indicate that the soils are accumulating mineral nutrients, probably as a result of long-term environmental disequilibrium.

California↗
USGS1990

Collection and analysis of colloidal particles transported in the Mississippi River, U.S.A.

Sediment transport has long been recognized as an important mechanism for the transport of contaminants in surface waters. Suspended sediment has traditionally been divided into three size classes: sand-sized (>63 ??m), silt-sized (<63 ??m but settleable) and clay-sized (non-settleable). The first two classes are easily collected and characterized using screens (sand) and settling (silt). The clay-sized particles, more properly called colloids, are more difficult to collect and characterize, and until recently received little attention. From the hydrologic perspective, a colloid is a particle, droplet, or gas bubble with at least one dimension between 0.001 and 1 ??m. Because of their small size, colloids have large specific surface areas and high surface free energies which may facilitate sorption of hydrophobic materials. Understanding what types of colloids are present in a system, how contaminants of interest interact with these colloids, and what parameters control the transport of colloids in natural systems is critical if the relative importance of colloid-mediated transport is to be understood. This paper describes the collection, concentration and characterization of colloidal materials in the Mississippi River. Colloid concentrations, particle-size distributions, mineral composition and electrophoretic mobilities were determined. Techniques used are illustrated with samples collected at St. Louis, Missouri, U.S.A.Sediment transport has long been recognized as an important mechanism for the transport of contaminants in surface waters. Suspended sediment has traditionally been divided into three size classes: sand-sized (> 63 ??m), silt-sized (< 63 ??m but settleable) and clay-sized (non-settleable). The first two classes are easily collected and characterized using screens (sand) and settling (silt). The clay-sized particles, more properly called colloids, are more difficult to collect and characterize, and until recently received little attention. From the hydrologic perspective, a colloid is a particle, droplet, or gas bubble with at least one dimension between 0.001 and 1 ??m. Because of their small size, colloids have large specific surface areas and high surface free energies which may facilitate sorption of hydrophobic materials. Understanding what types of colloids are present in a system, how contaminants of interest interact with these colloids, and what parameters control the transport of colloids in natural systems is critical if the relative importance of colloid-mediated transport is to be understood. This paper describes the collection, concentration and characterization of colloidal materials in the Mississippi River. Colloid concentrations, particle-size distributions, mineral composition and electrophoretic mobilities were determined. Techniques used are illustrated with samples collected at St. Louis, Missouri, U.S.A.

Journal of Contaminant Hydrology↗
USGS1989

Geochemical expression of early diagenesis in middle Eocene-lower Oligocene pelagic sediments in the southern Labrador Sea, Site 647, ODP Leg 105

Geochemical analyses of the middle Eocene through lower Oligocene lithologic Unit IIIC (260-518 meters below sea floor [mbsf]) indicate a relatively constant geochemical composition of the detrital fraction throughout this depositional interval at Ocean Drilling Program (ODP) Site 647 in the southern Labrador Sea. The main variability occurs in redox-sensitive elements (e.g., iron, manganese, and phosphorus), which may be related to early diagenetic inability in anaerobic pore waters during bacterial decomposition of organic matter. Initial preservation of organic matter was mediated by high sedimentation rates (36 m/m.Y.). High iron (Fe) and manganese (Mn) contents are associated with carbonate concretions of siderite, manganosiderite, and rhodochrosite. These concretions probably formed in response to elevated pore-water alkalinity and total dissolved carbon dioxide (CO2) concentrations resulting from bacterial sulfate reduction, as indicated by nodule stable-isotope compositions and pore-water geochemistry. These nodules differ from those found in upper Cenozoic hemipelagic sequences in that they are not associated with methanogenesis. Phosphate minerals (carbonate-fluorapatite) precipitated in some intervals, probably as the result of desorption of phosphorus from iron and manganese during reduction. The bulk chemical composition of the sediments differs little from that of North Atlantic Quaternary abyssal red clays, but may contain a minor hydrothermal component. The silicon/ aluminum (Si/Al) ratio, however, is high and variable and probably reflects original variations in biagenic opal, much of which is now altered to smectite and/or opal CT. An increase in the sodium/potassium (Na/K) ratio in the upper Eocene corresponds to the beginning of coarser-grained feldspar flux to the site, possibly marking the onset of more vigorous deep currents. Although the Site 647 cores provide a nearly complete high-resolution, high-latitude Eocene-Oligocene record, the high sedimentation rate and somewhat unusual diagenetic conditions have led to variable alteration of benthic foraminifers and fine-fraction carbonate and have overprinted the original stable-isotope records. Planktonic foraminifers are less altered, but on the whole, there is little chance of sorting out the nature and timing of environmental change on the basis of our stable-isotope analyses.

Proceedings of the Ocean Drilling Program: Scienti↗
USGS1998

Oreshoot zoning in the Carlin-type Betze orebody, Goldstrike Mine, Eureka County, Nevada

Field and laboratory investigations of the giant Betze gold orebody, the largest Carlin-type deposit known, in the north-central Carlin trend, Nevada document that the orebody is composed of individual high-grade oreshoots that contain different geologic, mineralogic, and textural characteristics. The orebody is typical of many structurally controlled Carlin-type deposits, and is hosted in thin-bedded, impure carbonate or limy siltstone, breccia bodies, and intrusive or calc-silicate rock. Most ores in the Betze orebody are highly sheared or brecciated and show evidence of syndeformational hydrothermal deposition. The interplay between rock types and pre- and syn-structural events accounts for most of the distribution and zoning of the oreshoots. Hydrothermal alteration is scale dependent, either in broad, pervasive alteration patterns, or in areas related to various oreshoots. Alteration includes decarbonatization (~decalcification) of carbonate units, argillization (illite-clay), and silicification. Patterns of alteration zoning in and surrounding the Betze orebody define a large porous, dilated volume of rock where high fluid flow predominated. Local restriction of alteration to narrow illite- and clay-rich selvages around unaltered marble or calc-silicate rock phacoids implies that fluid flow favored permeable structures and deformed zones. Gold mainly is present as disseminated sub-micron-sized particles, commonly associated with Asñrich pyrite, although one type of oreshoot contains micron-size free gold. Oreshoots form a three-dimensional zoning pattern in the orebody within a WNW-striking structural zone of shearing and shear folding, termed the Dillon deformation zone (DDZ). Main types of oreshoots are: (1) rutile-bearing siliceous oreshoots; (2) illite-clay-pyrite oreshoots; (3) realgar- and orpiment-bearing oreshoots; (4) stibnite-bearing siliceous oreshoots; and (5) polymetallic oreshoots. Zoning patterns result from paragenetically early development of illite-clay-pyrite oreshoots during movement along the DDZ, and subsequent silicification and brecciation, associated with formation of the realgar- and orpiment-bearing, and stibnite-bearing oreshoots. Additional shear movement along the DDZ followed. Polymetallic oreshoots, which contain minerals rich in Hg, Cu, Zn, Ag, and native Au, were the last ores to form and overprint most earlier oreshoots. Ore textures, gouge, phyllonitic rock, alteration style, and previously documented isotopic and fluid-inclusion data, all indicate a weakly to moderately saline fluid that ascended and cooled during structural displacements. Changing conditions, due to water-wall rock reactions and P-T changes during deformation, are probably responsible for fluid variation that resulted in zoning of the different oreshoots during dynamic interaction of the Au-bearing fluid with the wall rock. This investigation indicates that isolated As-, Sb-, and Hg-rich ores are separate parts of a larger single gold system. This large gold system was contemporaneous with post-Jurassic brittle-ductile deformation, on the basis of deformed mineralized pods of the Jurassic Goldstrike pluton, and large-scale hydrothermal flow, and together they appear to be an integral part of the formation of some Carlin-type gold deposits in north-central Nevada.

Nevada↗
USGS1978

Geochemical map showing the distribution and abundance of copper in stream sediments in the Seward and Blying Sound quadrangles, Alaska

Reconnaissance geochemical and mineralogical sampling was done in the Seward and Blying Sound quadrangles during 1975 and 1976 as part of the Alaska Mineral Resources Assessment Program (AMRAP). This map shows the distribution and abundance of copper in stream-sediment samples. Stream-sediment samples were collected at 569 sites from active stream channels and locally, from the interface of streambeds with intermediate- to low-tide beaches. Most of the stream sediment is fine- to coarse-grained sand, with a clay-silt fraction in streams discharging from glaciers. The stream sediment samples were air dried and sieved through a 80-mesh (0.2 mm) sieve, and the minus-80 mesh fraction was saved for analysis. A split of each sample was analyzed for copper and 15 other elements by a semiquantitative spectrographic method (Grimes and Marranzino, 1968). Other splits were analyzed for gold and zinc by atomic absorption methods (Warren and others, 1969). Sample sites and copper values (in parts per million) are indicated on the map by symbols identified in the histogram. The weakly anomalous values are considered to be significant only where they were detected in stream-sediment or heavy-mineral concentrate samples that also contained strongly anomalous values of other metals such as arsenic, gold, lead or tungsten. The map shows two populations for copper in stream sediments. One population consisting of generally lower copper values represents the samples collected from the sedimentary terrane in the central and western parts of the quadrangles. The other population consisting of generally higher copper values includes samples collected in areas of sheeted basalt dikes and pillow basalts in the eastern part of the quadrangles and from the sedimentary terrane of Latouche Island; in these areas chalcopyrite and pyrite were observed as fine-grained disseminations in the rocks and as mineral particles in the heavy-mineral concentrates.

Alaska↗
USGS1962

Tuscaloosa formation in Tennessee

Late Cretaceous Tuscaloosa Formation occurs as discontinuous remnants that cap many of the ridges in the Western Highland Rim. Typically the formation consists of well-rounded, poorly sorted chert gravel which is trimodal in size distribution. The gravel fraction (mode 15 to 40+ mm) consists of Devonian and Mississippian chert and a small percentage of sandstone pebbles. The medium sand fraction (mode 0.5 mm) consists mainly of angular to well-rounded chert grains developed by attrition during transport. Well-rounded and frosted quartz grains also are present. The fine fraction (mode 0.15 mm) consists of clay, authi-genic (?) mica, and quartz. At its eastern limit the Tuscaloosa is locally well sorted and contains quartz pebbles and a large proportion of quartz sand. Also present in the same area are well-sorted, heavy-mineral-bearing sands and bimodal (0.04, 0.2 mm) siltstone, which contains sand-sized pellet aggregates and fragmentary plant fossils. The finest fraction (less than 0.044 mm) of both eastern and western facies of the Tuscaloosa consists of 60-80 per cent quartz, 5-30 per cent kaolin, and 5-30 per cent montmorillonite, all of which are present in Devonian and Mississippian bedrock. Minor exotic constituents include volcanic(?) glass and heavy minerals. The Mississippian chert gravel in the Tuscaloosa is of local origin, but the Devonian chert was transported from a western source. Other components from a western source are sandstone pebbles and frosted sand grains, both of which probably were derived from Cambrian or Ordovician formations that cropped out on the Pascola arch, an eastward-sloping extension of the Ozark dome. Quartz pebbles, heavy minerals, and some of the angular quartz sand present at the eastern edge of the Tuscaloosa may have been derived from Pennsylvanian sandstone and conglomerates that cropped out north and south of the Pascola arch. Most of the Tuscaloosa Formation is believed to be of nonmarine origin, deposited on the eastward-sloping flank of the Pascola arch. The eastern facies of the Tuscaloosa is believed to be partly marine in origin, the exotic components having been swept in by longshore currents. During deposition of the Tuscaloosa , the Ozark dome and the Cincinnati arch were connected by the Pascola arch, which is now deeply buried beneath the Mississippi Embayment, At that time the Pascola arch stood structurally about 3000 feet higher than at present, and its structural shape and dimensions were comparable to the present Nashville dome. During deposition of the Tuscaloosa the Nashville dome was structurally about 1000 feet lower than at present, and its crest probably was submerged beneath the sea.

Tennessee↗
USGS1995

Estimated discharge and chemical-constituent loading from the upper Floridan aquifer to the lower St. Johns River, northeastern Florida, 1990-91

The lower St. Johns River, a 101-mile long segment of the St. Johns River, begins at the confluence of the Ocklawaha River and ends where the river discharges into the Atlantic Ocean at Mayport. The St. Johns River is affected by tides as far upstream as Lake George, 106 miles from the mouth. Saltwater from the ocean advances inland during each incoming tide and recedes during each outgoing tide. The chemical quality of the lower St. Johns River is highly variable primarily because of the inflow of saltwater from the ocean, and in some areas, from the discharge of mineralized ground water. Three hydrogeologic units are present in the study area: the surficial aquifer system, the intermediate confining unit, and the Floridan aquifer system. The surficial aquifer system overlies the intermediate confining unit and consists of deposits containing sand, clay, shell, and some limestone and dolomite. The intermediate confining unit underlies all of the study area and retards the vertical movement of water between the surficial aquifer system and the Floridan aquifer system. The intermediate confining unit consists of beds of relatively low permeability sediments that vary in thickness and areal extent and can be breached by sinkholes, fractures, and other openings. The Floridan aquifer system primarily consists of limestone and dolomite. The quality of water in the Upper Floridan aquifer varies throughout the study area. Dissolved solids in water range from about 100 to more than 5,000 milligrams per liter. Chloride and sulfate concentrations in water from the Upper Floridan aquifer range from about 4 to 3,700 milligrams per liter and from 1 to 1,300 milligrams per liter, respectively. The rate of leakage through the intermediate confining unit is controlled by the leakance coefficient of the intermediate confining unit and by the head difference between the Upper Floridan aquifer and the surficial aquifer system. The total ground-water discharge from the Upper Floridan aquifer to the St. Johns River within the lower St. Johns River drainage basin, based on the potentiometric surface of the Upper Floridan aquifer in September 1990, was estimated to be 86 cubic feet per second. Total estimated ground-water discharge to the lower St. Johns River in September 1991, when heads in the Upper Floridan aquifer averaged about 4 feet higher than in 1990, was 133 cubic feet per second. The load of dissolved-solids that discharged from the Upper Floridan aquifer into the lower St. Johns River on the basis of September 1990 heads is estimated to be 47,000 tons per year. Estimated chloride and sulfate loads are 18,000 and 9,500 tons per year, respectively. Dissolved-solids, chloride, and sulfate loads discharging into the lower St. Johns River are estimated to be 81,000, 39,000, and 15,000 tons per year, respectively, on the basis of September 1991 heads.

Florida↗
USGS2012

Occurrence model for volcanogenic beryllium deposits

Current global and domestic mineral resources of beryllium (Be) for industrial uses are dominated by ores produced from deposits of the volcanogenic Be type. Beryllium deposits of this type can form where hydrothermal fluids interact with fluorine and lithophile-element (uranium, thorium, rubidium, lithium, beryllium, cesium, tantalum, rare earth elements, and tin) enriched volcanic rocks that contain a highly reactive lithic component, such as carbonate clasts. Volcanic and hypabyssal high-silica biotite-bearing topaz rhyolite constitutes the most well-recognized igneous suite associated with such Be deposits. The exemplar setting is an extensional tectonic environment, such as that characterized by the Basin and Range Province, where younger topaz-bearing igneous rock sequences overlie older dolomite, quartzite, shale, and limestone sequences. Mined deposits and related mineralized rocks at Spor Mountain, Utah, make up a unique economic deposit of volcanogenic Be having extensive production and proven and probable reserves. Proven reserves in Utah, as reported by the U.S. Geological Survey National Mineral Information Center, total about 15,900 tons of Be that are present in the mineral bertrandite (Be 4 Si 2 O 7 (OH) 2 ). At the type locality for volcanogenic Be, Spor Mountain, the tuffaceous breccias and stratified tuffs that host the Be ore formed as a result of explosive volcanism that brought carbonate and other lithic fragments to the surface through vent structures that cut the underlying dolomitic Paleozoic sedimentary rock sequences. The tuffaceous sediments and lithic clasts are thought to make up phreatomagmatic base surge deposits. Hydrothermal fluids leached Be from volcanic glass in the tuff and redeposited the Be as bertrandite upon reaction of the hydrothermal fluid with carbonate clasts in lithic-rich sections of tuff. The localization of the deposits in tuff above fluorite-mineralized faults in carbonate rocks, together with isotopic evidence for the involvement of magmatic water in an otherwise meteoric water-dominated hydrothermal system, indicate that magmatic volatiles contributed to mineralization. At the type locality, hydrothermal alteration of dolomite clasts formed layered nodules of calcite, opal, fluorite, and bertrandite, the latter occurring finely intergrown with fluorite. Alteration assemblages and elemental enrichments in the tuff and surrounding volcanic rocks include regional diagenetic clays and potassium feldspar and distinctive hydrothermal halos of anomalous fluorine, lithium, molybdenum, niobium, tin, and tantalum, and intense potassium feldspathization with sericite and lithium-smectite in the immediate vicinity of Be ore. Formation of volcanogenic Be deposits is due to the coincidence of multiple factors that include an appropriate Be-bearing source rock, a subjacent pluton that supplied volatiles and heat to drive convection of meteoric groundwater, a depositional site characterized by the intersection of normal faults with permeable tuff below a less permeable cap rock, a fluorine-rich ore fluid that facilitated Be transport (for example, BeF 4 2- complex), and the existence of a chemical trap that caused fluorite and bertrandite to precipitate at the former site of carbonate lithic clasts in the tuff.

Scientific Investigations Report↗
USGS1945

Ground-water conditions in the vicinity of Carlsbad, New Mexico

The area included in this investigation lies in Eddy County, New Mexico, largely between the foothills of the Guadalupe Mountains on the west and the Pecos River on the east, and extends from Carlsbad southward to Black River. The Pecos River drains the entire area, and in the growing season when water is diverted at Avalon Dam for irrigation its flow in this locality is maintained largely by the numerous springs emerging in the river channel north of Carlsbad. Carlsbad and vicinity depend on ground water fro a domestic water supply as the waters of the Pecos River are too highly mineralized for domestic use. About 1,120 acres of land was irrigation by ground water in the vicinity of Carlsbad in 1940. Valley fill, of Quaternary age, extends over most of the area, largely as a thin veneer, but it has a maximum known thickness of 256 feet. It is made up largely of clay with lenses of conglomerate, gravel, and sand. The Rustler formation, of upper Permian age, underlies the fills and is composed of gypsum and red beds with one persistent bed of limestone. The Salado formation, which is composed chiefly of halite (common salt), underlies the Rustler formation elsewhere buy it is absent over most of the area described in this paper. This Castile formations, which is predominantly anhydrite, underlies the Salado and overlies the Delaware Mountain group, of middle Permian age, which is deeply buried in most of the area. The upper part of the Delaware Mountain group grades into the Capitan and Carlsbad limestones to the north, east, and west, the latter being exposed near Carlsbad and in the foothills of the Guadalupe Mountain. The Carlsbad limestone in turn grades into the upper part of the Chalk Bluff formation. Ground water apparently moves eastward from the Guadalupe Mountains through the Carlsbad limestone to recharge the aquifers in the Delaware Mountain, Castile, and Salado units. In these formations the water soon becomes too highly mineralized for domestic or irrigation use. A large part of the water in the Carlsbad limestone emerges in the spring area north of Carlsbad, and a part of it moves into the valley fill in Dark Canyon Arroyo. The water in the fill of Dark Canyon Arroyo moves laterally into the limestone of the Rustier formation. The water moving eastward in the valley fill and Rustier limestone becomes progressively more mineralized and in the farmland area in the Carlsbad Irrigation Dstrict it is unfit for domestic use. In addition, highly mineralized water seeping from the farmlands and canals in the Carlsbad Irrigation District commingles with the water from the west, and the resulting mixture is undesirable even for watering stock, although if necessity it is much used for that purpose. Water occurs in channels of the Carlsbad limestone, and wells drilled into it generally obtain large yields id hard but potable water. The municipal supply of the city of Carlsbad is derived from 4 wells (1940) in the Carlsbad limestone. The aquifer has a high transmissibility in the vicinity of Carlsbad, as was shown by a test made on one of the wells owned by Southwestern Public Service Co. This well has a specific capacity of 275 gallons per minute per foot of drawdown. The present withdrawal of water from wells penetrating the aquifers in the Carlsbad limestone averages about 4 second-feet (about 2,600,00 gallons a day). The average flow emerging in the spring area in the Pacos River north of Carlsbad is about 60 second-feet (about 40 million gallons a day). It appears that about 12 second-feet of this flow (about 8 million gallons a day) comes from aquifers in the Carlsbad limestone and that the remainder represents leakage from Lake Avalon and the canal system. The valley fill is less permeable than the Carlsbad limestone but in some places sufficient yields are obtained for irrigation purposes. A test made on a well in the fill just south of Carlsbad showed the aquifer in that locality to have a transmissibility of about 60,000. Contamination of the household wells in West Carlsbad does not appear to be taking place at the present time although the juxtaposition of cesspools and outhouses on the one hand and poorly cased wells for domestic water supply on the other makes the situation dangerous.

New Mexico↗