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At least 163 records · Page 9Linked to original sources

USGS2013

Temporal and spatial distribution of alteration, mineralization and fluid inclusions in the transitional high-sulfidation epithermal-porphyry copper system at Red Mountain, Arizona

Red Mountain, Arizona, is a Laramide porphyry Cu system (PCD) that has experienced only a modest level of erosion compared to most other similar deposits in the southwestern United States. As a result, the upper portion of the magmatic–hydrothermal system, which represents the transition from shallower high-sulfidation epithermal mineralization to deeper porphyry Cu mineralization, is well preserved. Within the Red Mountain system, alteration, mineralization and fluid inclusion assemblages show a systematic distribution in both time and space. Early-potassic alteration (characterized by the minerals biotite and magnetite) is paragenetically earlier than late-potassic alteration (K-feldspar–anhydrite) and both are followed by later phyllic (sericite–pyrite) alteration. Advanced argillic alteration (pyrophyllite–alunite–other clay minerals) is thought to be coeval with or postdate phyllic alteration. Minerals characteristic of advanced argillic alteration are present in the near surface. Phyllic alteration extends to greater depths compared to advanced argillic alteration. Early-potassic and late-potassic alteration are only observed in the deepest part of the system. Considerable overlap of phyllic alteration with both early-potassic and late-potassic alteration zones is observed. The hypogene mineralization contains 0.4–1.2% Cu and is spatially and temporally related to the late-potassic alteration event. Molybdenum concentration is typically < 300 ppm but positive anomalies (between 600 and 1200 ppm) occur, and typically correlate with the zones of higher Cu grades. Silver and Au range up to 50 ppm and 1 ppm, respectively, and mostly occur in the deeper parts of the system. Individual assays of up to 18 ppm Au and 274 ppm Ag in the shallower part of the system are interpreted to be associated with areas of highly focused fluid flow (i.e., breccias and thick veins). A near-surface, discontinuous chalcocite blanket is represented by scattered Cu anomalies within the mixed oxide/sulfide zone and its discontinuous nature may reflect differential permeability along fractures and faults. In the deepest part of the system, an early generation of low-to-moderate density and salinity liquid + vapor inclusions with opaque daughter minerals is followed in time by halite-bearing inclusions that also contain opaque daughter minerals indicating that an early intermediate-density magmatic fluid evolved to a high-density, high-salinity mineralizing fluid. The increase in density and salinity of fluids with time observed in the deeper parts of the system may be the result of immiscibility (“boiling”) of the earlier magmatic fluids or may reflect the compositional evolution of fluids that exsolved from the magma. Trails of inclusions consisting of only vapor-rich inclusions are common in the shallow parts of the system, and are associated with advanced argillic alteration, suggesting that intense boiling (“flashing”) occurred at (or below) this level. Fluid inclusion assemblages consisting of coexisting vapor-rich and halite-bearing inclusions are observed in samples extending from the surface to the upper part of the late-potassic zone, indicating that fluid immiscibility occurred within this depth interval.

Arizona↗

USGS2011

What makes a natural clay antibacterial?

Natural clays have been used in ancient and modern medicine, but the mechanism(s) that make certain clays lethal against bacterial pathogens has not been identified. We have compared the depositional environments, mineralogies, and chemistries of clays that exhibit antibacterial effects on a broad spectrum of human pathogens including antibiotic resistant strains. Natural antibacterial clays contain nanoscale (<200 nm), illite-smectite and reduced iron phases. The role of clay minerals in the bactericidal process is to buffer the aqueous pH and oxidation state to conditions that promote Fe 2+ solubility. Chemical analyses of E. coli killed by aqueous leachates of an antibacterial clay show that intracellular concentrations of Fe and P are elevated relative to controls. Phosphorus uptake by the cells supports a regulatory role of polyphosphate or phospholipids in controlling Fe 2+ . Fenton reaction products can degrade critical cell components, but we deduce that extracellular processes do not cause cell death. Rather, Fe 2+ overwhelms outer membrane regulatory proteins and is oxidized when it enters the cell, precipitating Fe 3+ and producing lethal hydroxyl radicals.

Environmental Science & Technology↗

USGS2001

Formation and use of coal combustion residues from three types of power plants burning Illinois coals

Coal, ash, and limestone samples from a fluidized bed combustion (FBC) plant, a pulverized coal combustion (PC) plant, and a cyclone (CYC) plant in Illinois were analyzed to determine the combustion behavior of mineral matter, and to propose beneficial uses for the power plant ashes. Pyrite and marcasite in coal were converted during combustion to glass, hematite and magnetite. Calcite was converted to lime and anhydrite. The clay minerals were altered to mullite and glass. Quartz was partially altered to glass. Trace elements in coal were partially mobilized during combustion and, as a result, emitted into the atmosphere or adsorbed on fly ash or on hardware on the cool side of the power plants. Overall, the mobilities of 15 trace elements investigated were lower at the FBC plant than at the other plants. Only F and Mn at the FBC plant, F, Hg, and Se at the PC plant and Be, F, Hg, and Se at the CYC plant had over 50% of their concentrations mobilized. Se and Ge could be commercially recovered from some of the combustion ashes. The FBC ashes could be used as acid neutralizing agents in agriculture and waste treatment, and to produce sulfate fertilizers, gypsum wall boards, concrete, and cement. The PC and CYC fly ashes can potentially be used in the production of cement, concrete, ceramics, and zeolites. The PC and CYC bottom ashes could be used in stabilized road bases, as frits in roof shingles, and perhaps in manufacturing amber glass. ?? 2001 Elsevier Science Ltd. All rights reserved.

Fuel↗

USGS2021

The role of hydrates, competing chemical constituents, and surface composition on CLNO2 formation

Atomic chlorine (Cl • ) affects air quality and atmospheric oxidizing capacity. Nitryl chloride (ClNO 2 ) – a common Cl • source–forms when chloride-containing aerosols react with dinitrogen pentoxide (N 2 O 5 ). A recent study showed that saline lakebed (playa) dust is an inland source of particulate chloride (Cl – ) that generates high ClNO 2 . However, the underlying physiochemical factors responsible for observed yields are poorly understood. To elucidate these controlling factors, we utilized single particle and bulk techniques to determine the chemical composition and mineralogy of playa sediment and dust samples from the southwest United States. Single particle analysis shows trace highly hygroscopic magnesium and calcium Cl-containing minerals are present and likely facilitate ClNO 2 formation at low humidity. Single particle and mineralogical analysis detected playa sediment organic matter that hinders N 2 O 5 uptake as well as 10 Å-clay minerals (e.g., Illite) that compete with water and chloride for N 2 O 5 . Finally, we show that the composition of the aerosol surface, rather than the bulk, is critical in ClNO 2 formation. These findings underscore the importance of mixing state, competing reactions, and surface chemistry on N 2 O 5 uptake and ClNO 2 yield for playa dusts and, likely, other aerosol systems. Therefore, consideration of particle surface composition is necessary to improve ClNO 2 and air quality modeling.

Environmental Science Technology↗

USGS2001

Updip limit of the seismogenic zone beneath the accretionary prism of southwest Japan: An effect of diagenetic to low-grade metamorphic processes and increasing effective stress

Off southwest Japan the seaward limit of coseismic displacement (or updip limit of the seismogenic zone) of the 1946 M w 8.3 thrust earthquake reaches to 4 km depth and ∼40 km landward of the trench. This limit coincides with the estimated location of the 150 °C isotherm, and has been linked to changes in physical properties associated with the smectite to illite clay-mineral transition. Here we show that this limit correlates with a suite of diagenetic to low-grade metamorphic processes characterized by (1) declining fluid production and decreasing fluid pressure ratio (λ * ) and (2) active clay, carbonate, and zeolite cementation and the transition to pressure solution and quartz cementation. These diagenetic to low-grade metamorphic changes cause the onset of velocity weakening during thrust faulting, an increase in effective stress, and strengthening of the hanging wall, which together combine to produce recordable earthquakes.

Geology↗

USGS2008

Holocene debris flows on the Colorado Plateau: The influence of clay mineralogy and chemistry

Holocene debris flows do not occur uniformly on the Colorado Plateau province of North America. Debris flows occur in specific areas of the plateau, resulting in general from the combination of steep topography, intense convective precipitation, abundant poorly sorted material not stabilized by vegetation, and the exposure of certain fine-grained bedrock units in cliffs or in colluvium beneath those cliffs. In Grand and Cataract Canyons, fine-grained bedrock that produces debris flows contains primarily single-layer clays—notably illite and kaolinite—and has low multilayer clay content. This clay-mineral suite also occurs in the colluvium that produces debris flows as well as in debris-flow deposits, although unconsolidated deposits have less illite than the source bedrock. We investigate the relation between the clay mineralogy and major-cation chemistry of fine-grained bedrock units and the occurrence of debris flows on the entire Colorado Plateau. We determined that 85 mapped fine-grained bedrock units potentially could produce debris flows, and we analyzed clay mineralogy and major-cation concentration of 52 of the most widely distributed units, particularly those exposed in steep topography. Fine-grained bedrock units that produce debris flows contained an average of 71% kaolinite and illite and 5% montmorillonite and have a higher concentration of potassium and magnesium than nonproducing units, which have an average of 51% montmorillonite and a higher concentration of sodium. We used multivariate statistics to discriminate fine-grained bedrock units with the potential to produce debris flows, and we used digital-elevation models and mapped distribution of debris-flow producing units to derive a map that predicts potential occurrence of Holocene debris flows on the Colorado Plateau.

Arizona, Colorado, New Mexico, Utah↗

USGS2010

Holocene variations in mineral and grain-size composition along the East Greenland glaciated margin (ca 67°–70°N): local versus long-distance sediment transport

Quantitative X-Ray Diffraction (qXRD) analysis of the <2 mm sediment fraction from surface (sea floor) samples, and marine sediment cores that span the last 10-12 cal ka BP, are used to describe spatial and temporal variations in non-clay mineral compositions for an area between Kangerlussuaq Trough and Scoresby Sund (???67??-70??N), East Greenland. Bedrock consists primarily of an early Tertiary alkaline complex with high weight% of pyroxene and plagioclase. Farther inland and to the north, the bedrock is dominantly felsic with a high fraction of quartz and potassium feldspars. Principal Component (PC) analysis of the non-clay sediment compositions indicates the importance of quartz and pyroxene as compositional end members, with an abrupt shift from quartz and k-feldspar dominated sediments north of Scoresby Sund to sediments rich in pyroxene and plagioclase feldspars offshore from the early Tertiary basaltic outcrop. Coarse (<2 mm or <1 mm) ice-rafted sediments are largely absent from the trough sediments between ???8 and 5 cal ka BP, but then increase in the last 4 cal ka BP. Compositional unmixing of the sediments in Grivel Basin and Kangerlussuaq Trough indicate the dominance of local over long distance sediment sources, with pulses of sediment from tidewater glaciers in Kangerlussuaq and Nansen fjords reaching the inner shelf during the Neoglaciation. The change in IRD is more dramatic in the sediment grain-size proxies than in the quartz wt%. Forty to seventy percent of the variance in the quartz records from either side of Denmark Strait is explained by low frequency trends, but the data from the Grivel Basin, East Greenland, are distinctly different, with an approximate 2500 yr periodicity. ?? 2010 Elsevier Ltd.

Quaternary Science Reviews↗

USGS2014

Spatial and stratigraphic distribution of water in oil shale of the Green River Formation using Fischer Assay, Piceance Basin, northwestern Colorado

The spatial and stratigraphic distribution of water in oil shale of the Eocene Green River Formation in the Piceance Basin of northwestern Colorado was studied in detail using some 321,000 Fischer assay analyses in the U.S. Geological Survey oil-shale database. The oil-shale section was subdivided into 17 roughly time-stratigraphic intervals, and the distribution of water in each interval was assessed separately. This study was conducted in part to determine whether water produced during retorting of oil shale could provide a significant amount of the water needed for an oil-shale industry. Recent estimates of water requirements vary from 1 to 10 barrels of water per barrel of oil produced, depending on the type of retort process used. Sources of water in Green River oil shale include (1) free water within clay minerals; (2) water from the hydrated minerals nahcolite (NaHCO 3 ), dawsonite (NaAl(OH) 2 CO 3 ), and analcime (NaAlSi 2 O 6 .H 2 0); and (3) minor water produced from the breakdown of organic matter in oil shale during retorting. The amounts represented by each of these sources vary both stratigraphically and areally within the basin. Clay is the most important source of water in the lower part of the oil-shale interval and in many basin-margin areas. Nahcolite and dawsonite are the dominant sources of water in the oil-shale and saline-mineral depocenter, and analcime is important in the upper part of the formation. Organic matter does not appear to be a major source of water. The ratio of water to oil generated with retorting is significantly less than 1:1 for most areas of the basin and for most stratigraphic intervals; thus water within oil shale can provide only a fraction of the water needed for an oil-shale industry.

Colorado↗

USGS2014

Spatial and stratigraphic distribution of water in oil shale of the Green River Formation using Fischer assay, Piceance Basin, northwestern Colorado

Colorado↗

USGS1985

Digital image processing techniques for detecting surface alteration - An application on the Alaska Peninsula: A section in The United States Geological Survey in Alaska: Accomplishments during 1983

The tectonic evolution of the Alaska Peninsula makes it a likely area for the discovery of significant mineral deposits. However, because of problems associated with remoteness and poor weather, little detailed mineral exploration work has been carried on there. This study focuses on using Landsat multispectral scanner data for the Port Moller, Stepovak Bay, and Simeon of Island Quadrangles to detect surface alteration, probably limonitic (iron oxide staining) and(or) argillic (secondary clay minerals) in character, that could be indicative of mineral deposits. The techniques used here are useful for mapping deposits that have exposed surface alteration of at least an hectare, the approximate spatial resolution of the Landsat data. Virtually cloud-free Landsat coverage was used, but to be detected, the alteration area must also be unobscured by vegetation. Not all mineral deposits will be associated with surface alteration, and not all areas of surface alteration will have valuable mineral deposits.

Alaska↗

USGS2001

Impact of climate and parent material on chemical weathering in Loess-derived soils of the Mississippi River valley

Peoria Loess-derived soils on uplands east of the Mississippi River valley were studied from Louisiana to Iowa, along a south-to-north gradient of decreasing precipitation and temperature. Major element analyses of deep loess in Mississippi and Illinois show that the composition of the parent material is similar in the northern and southern parts of the valley. We hypothesized that in the warmer, wetter parts of the transect, mineral weathering should be greater than in the cooler, drier parts of the transect. Profile average values of CaO/TiO 2 , MgO/TiO 2 , K 2 O/TiO 2 and Na 2 O/TiO 2 , Sr/Zr, Ba/Zr, and Rb/Zr represent proxies for depletion of loess minerals such as calcite, dolomite, hornblende, mica, and plagioclase. All ratios show increases from south to north, supporting the hypothesis of greater chemical weathering in the southern part of the valley. An unexpected result is that profile average values of Al 2 O 3 /TiO 2 and Fe 2 O 3 /TiO 2 (proxies for the relative abundance of clay minerals) show increases from south to north. This finding, while contrary to the evidence of greater chemical weathering in the southern part of the transect, is consistent with an earlier study which showed higher clay contents in Bt horizons of loess-derived soils in the northern part of the transect. We hypothesize that soils in the northern part of the valley received fine-grained loess from sources to the west of the Mississippi River valley either late in the last glacial period, during the Holocene or both. In contrast, soils in the southern part of the valley were unaffected by such additions.

Arkansas, Illinois, Iowa, Kentucky, Louisiana, Mis↗

USGS1987

Hydrogeologic and water-quality characteristics of glacial-drift aquifers in Minnesota

Water in Minnesota 's glacial drift aquifers generally is of acceptable quality for most uses, including household supply, industrial use, and irrigation. The aquifers generally contain calcium magnesium bicarbonate-type waters, but other types are present also. Calcium magnesium sulfate-type waters are common in the confined drift aquifers in the southwestern and northwestern parts of the State. The elevated concentrations of sulfate, which exceed limits recommended for drinking water by the EPA, results mainly from solution of sulfate bearing minerals in rocks of Cretaceous age that have been reworked in deep glacial drift. Sodium and chloride-type waters are common in drift aquifers in northwestern Minnesota owing to the inflow of saline water from bedrock aquifers of Paleozoic age North Dakota. Cation exchange with clay minerals in the drift also is a source of sodium to these waters, particularly in the confined drift aquifers. Some of the water from these aquifers are unsuitable for irrigation because of elevated concentrations of sodium, and some are unsuitable for drinking because of elevated concentrations of chloride. Concentrations of nitrite plus nitrate (as N) locally exceed the EPA recommended limits for drinking water in central and northwestern Minnesota. Shallow, unconfined drift aquifers are particularly susceptible to nitrate contamination from land surface. Confined drift aquifers are much less susceptible because overlying till deposits retard downward movement of contaminants to the deeper aquifers. Nitrate contamination, which may cause methemoglobinemia in infants, is one of the more serious water quality concerns in Minnesota. Iron and manganese concentrations commonly exceed EPA 's recommendations for drinking water throughout the State, but these constituents affect aesthetic properties of water rather than health.

Minnesota↗

USGS1956

Silica in hot-spring waters

The silica in hot-spring waters and in a few cold waters was studied by moans of the colorimetrie ammonium-molybdate method of analysis. Murata found in 1947 that only a part of the total silica in aged samples of high-silica waters was determinable by the colorimetric method. Weitz , franck And schuchard later showed that ammonium molybdate reacts readily with the monomeric form of silica (probably H 4 SiO 4 ) but very slowly with polymeric silica. If the colorimetric measurement is completed in two or three minutes, only the monomer is determined. Nearly all silica of hot springs is in the monomeric form. Solubility equilibrium exists between dissolved (monomeric) and amorphous silica. For the hot springs that were studied, the solubility is about 315 p.p.m. at 90°C and 110 p.p.m. at 25°C, which is very similar to Krauskopf's experimental data. Monomeric silica polymerizes so slowly to colloidal silica that many waters are supersaturated with respect to amorphous silica. The rate of polymerization is influenced by pH, temperature, degree of supersaturation, presence of previously formed colloidal and gelatinous silica and contact with opal and other substances. Supersaturated acid waters and alkaline waters with less than 100% supersaturation tend to remain supersaturated almost indefinitely, with little or no change. Precipitation of colloidal silica is favoured by high temperature and contact with opal. Many connate and other ground waters, including some thermal springs, are much below saturation with respect to amorphous silica, probably because low-solubility quartz and chalcedony have been precipitating. Quartz is favoured by relatively high temperature, slow rale of precipitation, and low degree of supersaturation, and is believed to form by deposition of monomeric molecules. Chalcedony is probably deposited when the degree of supersaturation is moderately high and the rate of deposition is relatively fast. The ranges of temperature over which quartz and chalcedony deposit no doubt overlap, but, if other factors are equal, quartz is favoured by high temperature. Opal is favoured by relatively low temperature and rapid rate of precipitation. Although opal has probably been deposited at temperatures as high as 140°C, it is unstable and is slowly converted to chalcedony or quartz. Water that is saturated with respect to opal is highly supersaturated with respect to quartz. Opal is probably formed from monomeric or more probably, the smaller polymeric molecules of silica, retaining some of their water content. Evidence is lacking for the direct conversion of gelatinous silica to opal. Some differences in solubility probably exist between amorphous opal and opal that shows X-ray patterns like that of cristobalite. The suggestion is made that clay minerals form by combination of monomeric silica and a comparable form of monomeric alumina, which must have very low solubility in waters within the pH range of 5 to 9. Because of the abundance and relatively high solubility of silica, the proposed reaction, dissolved alumina + dissolved silica ⇌ clay, is ordinarily displaced strongly to the right in hydrothermal alteration and in ordinary soil formation. With removal of free silica, aided by tropical rainfall and temperatures, the reaction may be displaced to the left by dissolution and removal of silica from the system. Alumina, because of its very low solubility, remains as bauxite.

Geochimica et Cosmochimica Acta↗

USGS2008

The evolution of volcano-hosted geothermal systems based on deep wells from Karaha-Telaga Bodas, Indonesia

Temperature and pressure surveys, fluid samples, and petrologic analyses of rock samples from deep drill holes at the Karaha - Telaga Bodas geothermal field on the volcanic ridge extending northward from Galunggung Volcano, West Java, have provided a unique opportunity to characterize the evolution of an active volcano-hosted geothermal system. Wells up to 3 km in depth have encountered temperatures as high as 353??C and a weakly altered granodiorite that intruded to within 2 to 3 km of the surface. The intrusion is shallowest beneath the southern end of the field where an acid lake overlies a nearly vertical low resistivity structure (<10 ohm-m) defined by magnetotelluric measurements. This structure is interpreted to represent a vapor-dominated chimney that provides a pathway to the surface for magmatic gases. Four distinct hydrothermal mineral assemblages document the evolution of the geothermal system and the transition from liquid- to vapor-dominated conditions. The earliest assemblage represents the initial liquid-dominated system generated during emplacement of the granodiorite between 5910 ?? 76 and 4200 ?? 150 y BP. Tourmaline, biotite, actinolite, epidote and clay minerals were deposited contemporaneously at progressively greater distances from the intrusive contact (assemblage 1). At 4200 ?? 150 y BP, flank collapse and the formation of the volcano's crater, Kawah Galunggung, resulted in catastrophic decompression and boiling of the hydrothermal fluids. This event initiated development of the modern vapor-dominated regime. Chalcedony and then quartz were deposited as the early low salinity liquids boiled (assemblage 2). Both vapor- and liquid-rich fluid inclusions were trapped in the quartz crystals. Liquid-rich fluid inclusions from the southern part of the field record salinities ranging from 0 to 26 weight percent NaCl- CaCl2 equivalent and locally contain fluorite daughter crystals. We suggest, based on temperature-salinity relationships and evidence of boiling, that these fluids were progressively concentrated as steam was lost from the system. However, mixing with fluids derived from the underlying intrusion or generated during the formation of acid SO4 water on the vapor-dominated chimney margins could have contributed to the observed salinities. As pressures declined, CO2- and SO4-rich steam-heated water drained downward, depositing anhydrite and calcite (assemblage 3) in the fractures, limiting further recharge. Fluid inclusions with salinities up to 31 weight percent NaCl equivalent were trapped in these minerals as the descending water vaporized. The final assemblage is represented by precipitates of NaCl, KCl and FeClx deposited on rock surfaces in portions of the vapor-dominated zone that boiled dry. Vapor-dominated conditions extend over a distance of at least 10 km and to depths below sea level. Deep wells drilled into the underlying liquid-dominated reservoir in the northern and central part of the volcanic ridge produce low salinity fluids representing recent recharge of meteoric and steam-heated water. The evolution of volcanic-hosted vapor-dominated geothermal systems can be described by a five stage model. Stage 1 involves the formation of an over-pressured liquid-dominated geothermal system soon after magmatic intrusion. In Stages 2 and 3, pressures progressively decrease, and a curtain of steam-heated water surrounding a magmatic vapor-dominated chimney at 350??C and 14 ?? 2 MPa develops. The relatively low pressure near the base of the chimney causes liquid inflow adjacent to the intrusion and the development of a secondary marginal vapor-dominated zone. In Stage 4, the magmatic vapor discharge from the intrusion becomes small, vapor pressure declines, and the secondary vapor-dominated zone expands above the intrusion. In Stage 5, the vapor-dominated zone floods because heat from the intrusion is insufficient to boil all liquid inflow. A more common, liquid-dominated volcanic-hosted system the

American Journal of Science↗

USGS2019

Controls on organic matter distributions in Eocene Lake Uinta, Utah and Colorado

The Green River Formation deposited in Eocene Lake Uinta in the Uinta and Piceance Basins, Utah and Colorado, contains the largest oil shale resource in the world with an estimated 1.53 trillion barrels of oil in-place in the Piceance Basin and 1.32 trillion barrels in the Uinta Basin. The Douglas Creek arch, a slowly subsiding hinge-line between the two basins, created separate deep depocenters with shallow water conditions near the crest of the arch. Lake Uinta was a saline lake throughout its history with a lower saline to hypersaline layer (monimolimnion) and an upper less saline layer (mixolimnion). Most of the organic matter in the Green River Formation was derived primarily from algae that lived in the photic zone of the lake and is very hydrogen-rich and oil-prone. In many modern large and deep lakes, rates of organic matter production are highly variable due to differences in nutrient supply. However, cyclonic circulation often leads to winnowing out organic and mineral matter in the mixolimnion leading to organic and fine-grained mineral matter being deposited in increasing amounts toward hydro-dynamically dead zones in the center of the circulation producing concentric bands of increasing organic matter content. Organic matter transport through the dense, hypersaline monimolimnion may have been facilitated by low density organic matter attaching to more dense clay mineral particles. Most of the oil shale intervals deposited in Lake Uinta display similar patterns in their organic matter distributions, increasing in very regular fashion toward the central areas of the lake’s two depocenters. This concentric feature is particularly prominent in the most laminated oil shale zones. Here, we propose that cyclonic circulation was present in Lake Uinta. Each basin appears to have had its own circulation currents, separated by shallow water conditions near the Douglas Creek arch, as well as one hydro-dynamically dead zone. Sediment gravity flow processes were also very active in some strata of Lake Uinta, leading to the reworking and redepositing of sediments. Two general types of sediment gravity flows are recognized: (1) organic-rich sediment gravity flows that reworked and may have concentrated organic-rich material closer to the two deep depocenters, and (2) sandstone and siltstone-rich organic-poor mass movement deposits that originated on marginal shelves. Mass movements could have been triggered by various natural processes and/or possibly by the movement of dense brines that evolved on marginal shelves and moved along the bottom of the water column toward the deep part of the lake. The uppermost, poorly consolidated sediment layer was incorporated in sediment gravity flows as they moved, and in many cases sediment gravity flows scoured down significantly into the more consolidated underlying sediment producing large rip-up clasts of laminated sediments. Truncation of more than 100 ft occurs at the base of a sequence of sediment gravity flows in one well, indicating a significant incised channel. Coarser-grained sediment gravity flows terminated before reaching the lake’s deepest areas, forming thick concentric buildups of organically-lean sediment near the base of the marginal slopes. Intervals dominated by organic-rich fine-grained sediment gravity flows have tightly concentric bands of increasing organic matter toward the deepest parts of the lake and can be organically richer than the richest laminated intervals. There is some evidence that the hydro-dynamically quiet zones did not always correspond closely to the deepest areas of the lake, extending in some cases into shallower areas.

Colorado, Utah↗

USGS1981

Tertiary carbonate-dissolution cycles on the Sierra Leone Rise, eastern equatorial Atlantic Ocean

Most of the Tertiary section on Sierra Leone Rise off northwest Africa consists of chalk, marl, and limestone that show cyclic alterations of clay-rich and clay-poor beds about 20–60 cm thick. On the basis of biostratigraphic accumulation rates, the cycles in Oligocene and Miocene chalk have periods which average about 44,000 years, and those in Eocene siliceous limestone have periods of 4000–27,000 years. Several sections were sampled in detail to further define the cycles in terms of content of CaCO 3 , clay minerals, and relative abundances of calcareous nannofossils. Extending information gained by analyses of Pleistocene cores from the continental margin of northwest Africa to the Tertiary cycles on Sierra Leone Rise, both dilution by noncarbonate material and dissolution of CaCO 3 could have contributed to the observed relative variations in clay and CaCO 3 . However, dissolution of CaCO 3 as the main cause of the carbonate-clay cycles on the Sierra Leone Rise, rather than dilution by clay, is suggested by the large amount of change (several thousand percent) in terrigenous influx required to produce the observed variations in amount of clay and by the marked increase in abundance of dissolution-resistant discoasters relative to more easily dissolved coccoliths in low-carbonate parts of cycles. The main cause of dissolution of CaCO 3 was shoaling of the carbonate compensation depth (CCD) during the early Neogene and climatically induced fluctuations in the thickness of Antarctic Bottom Water.

Marine Geology↗

USGS1999

Determination of chemical-constituent loads during base-flow and storm-runoff conditions near historical mines in Prospect Gulch, upper Animas River watershed, southwestern Colorado

Prospect Gulch is a major source of iron, aluminum, zinc, and other metals to Cement Creek. Information is needed to prioritize remediation and develop strategies for cleanup of historical abandoned mine sites in Prospect Gulch. Chemical-constituent loads were determined in Prospect Gulch, a high-elevation alpine stream in southwestern Colorado that is affected by natural acid drainage from weathering of hydro-thermally altered igneous rock and acidic metal-laden discharge from historical abandoned mines. The objective of the study was to identify metal sources to Prospect Gulch. A tracer solution was injected into Prospect Gulch during water-quality sampling so that loading of geochemical constituents could be calculated throughout the study reach. A thunderstorm occurred during the tracer study, hence, metal loads were measured for storm-runoff as well as for base flow. Data from different parts of the study reach represents different flow conditions. The beginning of the reach represents background conditions during base flow immediately upstream from the Lark and Henrietta mines (samples PG5 to PG45). Other samples were collected during storm runoff conditions (PG100 to PG291); during the first flush of metal runoff following the onset of rainfall (PG303 to PG504), and samples PG542 to PG700 were collected during low-flow conditions. During base-flow conditions, the percentage increase in loads for major constituents and trace metals was more than an order of magnitude greater than the corresponding 36 % increase in stream discharge. Within the study reach, the highest percentage increases for dissolved loads were 740 % for iron (Fe), 465 % for aluminum (Al), 500 % for lead (Pb), 380 % for copper (Cu), 100 % for sulfate (SO4), and 50 % for zinc (Zn). Downstream loads near the mouth of Prospect Gulch often greatly exceeded the loads generated within the study reach but varied by metal species. For example, the study reach accounts for about 6 % of the dissolved-Fe load, 13 % of the dissolved-Al load, and 18 % of the dissolved-Zn load; but probably contributes virtually all of the dissolved Cu and Pb. The greatest downstream gains in dissolved trace-metal loads occurred near waste-rock dumps for the historical mines. The major sources of trace metals to the study reach were related to mining. The major source of trace metals in the reach near the mouth is unknown, however is probably related to weathering of highly altered igneous rocks, although an unknown component of trace metals could be derived from mining sources The late-summer storm dramatically increased the loads of most dissolved and total constituents. The effects of the storm were divided into two distinct periods; (1) a first flush of higher metal concentrations that occurred soon after rainfall began and (2) the peak discharge of the storm runoff. The first flush contained the highest loads of dissolved Fe, total and dissolved Zn, Cu, and Cd. The larger concentrations of Fe and sulfate in the first flush were likely derived from iron hydroxide minerals such as jarosite and schwertmanite, which are common on mine dumps in the Prospect Gulch drainage basin. Peak storm runoff contained the highest measured loads of total Fe, and of total and dissolved calcium, magnesium, silica and Al, which were probably derived from weathering of igneous rocks and clay minerals in the drainage basin.

Colorado↗

USGS1985

Comparative geochemical and mineralogical studies of two cyclic transgressive pelagic limestone units, cretaceous Western Interior Basin, U.S.

Pelagic limestone units were deposited in the North American Western Interior seaway during two major Cretaceous transgressive episodes. The Bridge Creek Limestone Member of the Greenhorn Formation, deposited during the Late Cenomanian-Early Turonian transgression, and the Smoky Hill Member of the Niobrara Formation, deposited during the overall Early Coniacian-Early Campanian transgression, are both enriched in organic-carbon and exhibit smallscale carbonate cycles representing periodicities in the range 20 to 40 ky. The distinct periodicity and overall unusual depositional milieu of both units are reflected in their sedimentary structures, mineralogy, and geochemistry. The Bridge Creek Limestone at Pueblo, Colorado, averages 78% CaCO 3 and 1.75% organic carbon with ranges of 42-96% and 0.06-6.97%, respectively, across small-scale cycles. High concentrations of Al, Fe, Mg, K, Ti, Na, Cr, Ni, V; higher Sr/Ca and lower Si/Al ratios; and lighter δ 18 0 in CaCO 3 in dark-colored clay-rich beds all suggest periodic influx of terrestrial clay minerals during times of peak fresh water runoff from uplifted highlands to the west. Higher Sr/Ca ratios in marlstone beds than in limestone beds suggest that the marlstone beds have undergone less diagenetic removal of Sr. Higher concentrations of organic carbon, hydrogen, and sulfur, and preservation of some lamination in the clay-rich beds also suggest that the times of enhanced runoff may have induced stable salinity stratification in the water column, which led to gradual depletion of dissolved oxygen in the bottom waters and enhanced preservation of organic carbon in sediments. The geochemistry also suggests that a significant change in sedimentation occurred at the Cenomanian-Turonian boundary. The geochemical characteristics of the Niobrara Formation near Fort collins, Colorado, are very similar to those of the Bridge Creek Limestone at Pueblo, suggesting similar depositional conditions and source of clastic materials. However, the small scale cycles are present but more subdued in the Niobrara Formation than in the Bridge Creek Limestone, and the Niobrara Formation in the Fort Collins area has not been as altered by diagenesis.

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