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At least 397 records · Page 22Linked to original sources

USGS2000

Regoliths of the middle-Atlantic Piedmont and evolution of a polymorphic landscape

The regolith overlying the alumino-silicate rocks of the middle-Atlantic Piedmont Province consists primarily of saprolite with a thin veneer of diamictons of colluvial origin. Thickness and distribution of the saprolite is related to landform and lithology. For example, on uplands isovolumetric weathering of the Loch Raven Schist produces saprolite averaging 55 ft (17 m) thick. On Port Deposit Gneiss, saprolite beneath uplands averages 42 ft (13 m) in thickness. The saprolite results from the reaction of alumino-silicate rocks with through-flowing groundwater. Chemical weathering of the rock results in clay and resistate minerals, residual rock layers, corestones, and pinnacles. Surface erosion of saprolite with quartzite and metagraywacke residual layers may produce a 'washboard' topography. Surface erosion of a metagabbro saprolite containing corestones and pinnacles results in a surface with lag deposits of corestones and emergent pinnacles. The diamicton material comes from the underlying saprolite, weathered rock and bedrock. Generally, diamictons are thinner on uplands and upper slopes, and thicker at the base of slopes and in hollows and gathering areas of first-order streams. The saprolite and colluvium reflect response of geomorphic processes (chemical weathering, fluvial incision, and periglacial processes) to rock lithology and landscape. The modifications to the landscape have been driven by neotectonic crustal warping and alternating periglacial-humid temperate climates. Altogether these varied interactions have resulted in a Holocene polymorphic landscape.

Southeastern Geology↗

USGS2003

Applied geochemistry, geology and mineralogy of the northernmost Carlin trend, Nevada

Investigations in the northernmost Carlin trend were undertaken to advance understanding of the geochemical signatures and genesis of precious metal deposits in the trend . Two fundamental geologic relationships near the trend significantly affect regional geochemical distributions: a remarkably intact lower Paleozoic stratigraphic sequence of siliceous rocks in the upper plate of the middle Paleozoic Roberts Mountains thrust, and the widespread repetition of rocks high in the upper plate during late Paleozoic thrusting that thickens the cover above mineralized rock in the lower plate. A compilation of previously published chemical analyses of 440 stream sediment samples and 115 rocks from two 7 1/2-minute quadrangles, as well as new chemical analyses of approximately 1,000 drill core samples in a 1,514 m (4,970 ft) hole through the Rodeo Creek deposit were used to construct three-dimensional element distribution models that highlight metal zonation in the mineralized systems. The Rodeo Creek deposit comprises deep Ag base-metal ± Au-mineralized rock below the Roberts Mountains thrust and contains an unusually high Ag/Au ratio greater than 30. Stacked geochemical halos related to the deposit are confined to the lower plate of the Roberts Mountains thrust and include two horizons of Hg, Cu, and Zn anomalies-as much as 180 m above the deposit-that mostly result from mercurian sphalerite. Extremely subtle indications of mineralization in the upper plate of the Roberts Mountains thrust above the deposit include arsenopyrite overgrowths on small pyrite crystals in 50- to 75-μm-wide clay-carbonate veinlets that lack alteration halos, arsenical rims on small disseminated crystal of recrystallized diagenetic pyrite, and partial replacement of diagenetic pyrite by tennantite. Some of these minerals contain anomalously high Au. However, these As-(Au)-bearing rocks most likely represent another locus of largely untested mineralized rock rather than distal halos related to either the Rodeo Creek or the nearby Dee and Storm gold deposits. Application of micromineralogic techniques helped to identify mineral assemblages that are specific to mineralization and provided an empirical foundation for interpretations of geochemical halos in the Carlin trend . District-scale geochemical patterns of several elements in stream sediments and surface rocks coincide with the northernmost Carlin trend and can be used to explore for Carlin -type deposits. Concentrations of elevated As and Sb in stream sediments (as much as 54 ppm As) have northwest-elongate lobate patterns that clearly outline the trend across a width of approximately 4 km. Arsenic contents of exposed rocks (as much as 90 ppm As) strongly correlate with As contents of derivative stream sediments, and rock contents of Sb show a somewhat lesser but nonetheless strong and similar correspondence. Factor analysis of stream-sediment data shows that those factor scores that are correlated with As, Sb, Au, and Pb also are high along the trend and suggest that mineralized rocks may be present. Although As was not detected by scanning electron microscope-energy dispersive spectrometer (SEM-EDS) studies in heavy mineral concentrates of high-As stream sediments in the Carlin trend , X-ray absorption near-edge spectra (XANES) of selected light fractions of stream sediment samples indicate that Al-bearing phases, such as gibbsite, amorphous Al oxyhydroxides, or aluminosilicate clay minerals host most of the As(V). The best fit, visually and in terms of the lowest residual, was obtained by a model compound of As(V) sorbed to gibbsite. Thus, most As in stream sediments derived from altered rock within the Carlin trend apparently is contained in light fractions. The geochemical character of young, unconsolidated, postmineral deposits that cover mineralized rocks on the Carlin trend partly results from mineralized sources along the trend . Concentration of As in the Miocene Carlin Formation shows an exceptionally well developed progressive increase to about 30 ppm As as altered rock surrounding the trend is approached. Mineralized and/or altered rock fragments probably have been shed directly into the sedimentary basin of the Carlin Formation, and migration of As, now fixed as As(V), also may have occurred in the supergene environment after material was recycled out of the Carlin Formation and into present-day gulleys.

Nevada↗

USGS1979

Sand dunes on the central Delmarva Peninsula, Maryland and Delaware

Inconspicuous ancient sand dunes are present in parts of the central Delmarva Peninsula, Maryland and Delaware. Many dunes are roughly V-shaped, built by northwest winds, especially on the east sides of some of the large rivers. On the uplands, the form and spacing of the dunes are variable. A surficial blanket composed mainly of medium and fine-grained sand-the Parsonsburg Sand-forms both the ancient dunes and the broad plains between the dunes. The sand that forms the dunes is massive and intensely burrowed in the upper part; traces of horizontal or slightly inclined bedding appear near the base. Quartz is the dominant mineral constituent of the sand. Microline is abundant in the very fine to fine sand fraction. The heavy-mineral assemblages (high zircon, tourmaline, rutile) are more mature than in most of the possible source rocks. The most abundant minerals in the clay-sized fraction are dioctahedral vermiculite, kaolinite, illite, montmorillonite, and gibbsite. The first four minerals are common in deposits of late Wisconsin and Holocene age. The gibbsite may be detrital, coming from weathered rocks of Tertiary age. The soil profile in the dune sand is weakly to moderately developed. At or near the base of the Parsonsburg Sand are peaty beds that range in age from about 30,000 to about 13,000 radiocarbon years B.P. Microfloral assemblages in the peaty beds suggest that the dunes on the uplands formed in a spruce parkland during the late Wisconsin glacial maximum. The river dunes may also be of late Wisconsin age, but could be Holocene.

Professional Paper↗

USGS2002

Mapped minerals at Questa, New Mexico, using airborne visible-infrared imaging spectrometer (AVIRIS) data – Preliminary report for: First quarterly report of the U.S. Geological Survey investigation of baseline and pre-mining ground-water quality in the Red River Valley Basin, New Mexico, November 13, 2001

This preliminary study for the First Quarterly Report has spectrally mapped hydrothermally altered minerals useful in assisting in assessment of water quality of the Red River. Airborne Visible-Infrared Imaging Spectrometer (AVIRIS) data was analyzed to characterize mined and unmined ground at Questa, New Mexico. AVIRIS data covers the Red River drainage north of the river, from between the town of Questa on the west, to east of the town of Red River. The data was calibrated and analyzed using U.S. Geological Survey custom software and spectral mineral library. AVIRIS data was tested for spectral features that matched similar features in the spectral mineral library. Goodness-of-fit and band-depth were calculated for each comparison of spectral features and used to identify surface mineralogy. Mineral distribution, mineral associations, and AVIRIS pixel spectra were examined. Mineral maps show the distribution of iron hydroxides, iron sulfates, clays, micas, carbonates, and other minerals. Initial results show a system of alteration suites that overprint each other. Quartz-sericite-pyrite (QSP) alteration grading out to propylitic alteration (epidote and calcite) was identified at the Questa Mine (molybdenum porphyry) and a similar alteration pattern was mapped at the landslide ("scar") areas. Supergene weathering overprints the altered rock, as shown by jarosite, kaolinite, and gypsum. In the spectral analysis, hydrothermally altered ground appears to be more extensive at the unmined Goat Hill Gulch and the mined ground, than the ?scars? to the east. Though the "scars" have similar overall altered mineral suites, there are differences between the "scars" in sericite, kaolinite, jarosite, gypsum, and calcite abundance. Fieldwork has verified the results at the central unmined "scar" areas.

New Mexico↗

USGS2017

Timescales of carbon turnover in soils with mixed crystalline mineralogies

Organic matter–mineral associations stabilize much of the carbon (C) stored globally in soils. Metastable short-range-order (SRO) minerals such as allophane and ferrihydrite provide one mechanism for long-term stabilization of organic matter in young soil. However, in soils with few SRO minerals and a predominance of crystalline aluminosilicate or Fe (and Al) oxyhydroxide, C turnover should be governed by chemisorption with those minerals. Here, we correlate mineral composition from soils containing small amounts of SRO minerals with mean turnover time (TT) of C estimated from radiocarbon ( 14 C) in bulk soil, free light fraction and mineral-associated organic matter. We varied the mineral amount and composition by sampling ancient soils formed on different lithologies in arid to subhumid climates in Kruger National Park (KNP), South Africa. Mineral contents in bulk soils were assessed using chemical extractions to quantify Fe oxyhydroxides and SRO minerals. Because of our interest in the role of silicate clay mineralogy, particularly smectite (2 : 1) and kaolinite (1 : 1), we separately quantified the mineralogy of the clay-sized fraction using X-ray diffraction (XRD) and measured 14 C on the same fraction. Density separation demonstrated that mineral associated C accounted for 40–70 % of bulk soil organic C in A and B1 horizons for granite, nephelinite and arid-zone gabbro soils, and > 80 % in other soils. Organic matter strongly associated with the isolated clay-sized fraction represented only 9–47 % of the bulk soil C. The mean TT of C strongly associated with the clay-sized fraction increased with the amount of smectite (2 : 1 clays); in samples with > 40 % smectite it averaged 1020 ± 460 years. The C not strongly associated with clay-sized minerals, including a combination of low-density C, the C associated with minerals of sizes between 2 µm and 2 cm (including Fe oxyhydroxides as coatings), and C removed from clay-sized material by 2 % hydrogen peroxide had TTs averaging 190 ± 190 years in surface horizons. Summed over the bulk soil profile, we found that smectite content correlated with the mean TT of bulk soil C across varied lithologies. The SRO mineral content in KNP soils was generally very low, except for the soils developed on gabbros under more humid climate that also had very high Fe and C contents with a surprisingly short, mean C TTs. In younger landscapes, SRO minerals are metastable and sequester C for long timescales. We hypothesize that in the KNP, SRO minerals represent a transient stage of mineral evolution and therefore lock up C for a shorter time. Overall, we found crystalline Fe-oxyhydroxides (determined as the difference between Fe in dithionate citrate and oxalate extractions) to be the strongest predictor for soil C content, while the mean TT of soil C was best predicted from the amount of smectite, which was also related to more easily measured bulk properties such as cation exchange capacity or pH. Combined with previous research on C turnover times in 2 : 1 vs. 1 : 1 clays, our results hold promise for predicting C inventory and persistence based on intrinsic timescales of specific carbon–mineral interactions.

SOIL↗

USGS2004

Common clay and shale

Part of the 2003 industrial minerals review. The legislation, production, and consumption of common clay and shale are discussed. The average prices of the material and outlook for the market are provided.

Mining Engineering↗

USGS2003

Field guide to hydrothermal alteration in the White River altered area and in the Osceola Mudflow, Washington

The Cenozoic Cascades arcs of southwestern Washington are the product of long-lived, but discontinuous, magmatism beginning in the Eocene and continuing to the present (for example, Christiansen and Yeats, 1992). This magmatism is the result of subduction of oceanic crust beneath the North American continent. The magmatic rocks are divided into two subparallel, north-trending continental-margin arcs, the Eocene to Pliocene Western Cascades, and the Quaternary High Cascades, which overlies, and is east of, the Western Cascades. Both arcs are calc-alkaline and are characterized by voluminous mafic lava flows (mostly basalt to basaltic andesite compositions) and scattered large stratovolcanoes of mafic andesite to dacite compositions. Silicic volcanism is relatively uncommon. Quartz diorite to granite plutons are exposed in more deeply eroded parts of the Western Cascades Arc (for example, Mount Rainier area and just north of Mt. St. Helens). Hydrothermal alteration is widespread in both Tertiary and Quaternary igneous rocks of the Cascades arcs. Most alteration in the Tertiary Western Cascades Arc resulted from hydrothermal systems associated with small plutons, some of which formed porphyry copper and related deposits, including copper-rich breccia pipes, polymetallic veins, and epithermal gold-silver deposits. Hydrothermal alteration also is present on many Quaternary stratovolcanoes of the High Cascades Arc. On some High Cascades volcanoes, this alteration resulted in severely weakened volcanic edifices that were susceptible to failure and catastrophic landslides. Most notable is the sector collapse of the northeast side of Mount Rainier that occurred about 5,600 yr. B.P. This collapse resulted in formation of the clay-rich Osceola Mudflow that traveled 120 km down valley from Mount Rainier to Puget Sound covering more than 200 km2. This field trip examines several styles and features of hydrothermal alteration related to Cenozoic magmatism in the Cascades arcs. The morning of the trip will examine the White River altered area, which includes high-level alteration related to a large, early Miocene magmatic-hydrothermal system exposed about 10 km east of Enumclaw, Washington. Here, vuggy silica alteration is being quarried for silica and advanced argillic alteration has been prospected for alunite. Clay-filled fractures and sulfide-rich, fine-grained sedimentary rocks of hydrothermal origin locally are enriched in precious metals. Many hydrothermal features common in high-sulfidation gold-silver deposits and in advanced argillic alteration zones overlying porphyry copper deposits (for example, Gustafson and Hunt, 1975; Hedenquist and others, 2000; Sillitoe, 2000) are exposed, although no economic base or precious metal mineralized rock has been discovered to date. The afternoon will be spent examining two exposures of the Osceola Mudflow along the White River. The Osceola Mudflow contains abundant clasts of altered Quaternary rocks from Mount Rainier that show various types of hydrothermal alteration and hydrothermal features. The mudflow matrix contains abundant hydrothermal clay minerals that added cohesiveness to the debris flow and helped allow it to travel much farther down valley than other, noncohesive debris flows from Mount Rainier (Crandell, 1971; Vallance and Scott, 1997). The White River altered area is the subject of ongoing studies by geoscientists from Weyerhaeuser Company and the U.S. Geological Survey (USGS). The generalized descriptions of the geology, geophysics, alteration, and mineralization presented here represent the preliminary results of this study (Ashley and others, 2003). Additional field, geochemical, geochronologic, and geophysical studies are underway. The Osceola Mudflow and other Holocene debris flows from Mount Rainier also are the subject of ongoing studies by the USGS (for example, Breit and others, 2003; John and others, 2003; Plumlee and others, 2003, Sisson and others, 2003; Vallance and others, 2003). Studies of hydrothermal alteration in the Osceola Mudflow are being used to better understand fossil hydrothermal systems on Mount Rainier and potential hazards associated with this alteration.

Washington↗

USGS2003

Common clay and shale

Part of the 2002 industrial minerals review. The production, consumption, and price of shale and common clay in the U.S. during 2002 are discussed. The impact of EPA regulations on brick and structural clay product manufacturers is also outlined.

Mining Engineering↗

USGS2001

Ball clay

Part of the 2000 annual review of the industrial minerals sector. A general overview of the ball clay industry is provided. In 2000, sales of ball clay reached record levels, with sanitary ware and tile applications accounting for the largest sales. Ball clay production, consumption, prices, foreign trade, and industry news are summarized. The outlook for the ball clay industry is also outlined.

Mining Engineering↗

USGS2010

Mineral and Vegetation Maps of the Bodie Hills, Sweetwater Mountains, and Wassuk Range, California/Nevada, Generated from ASTER Satellite Data

Multispectral remote sensing data acquired by the Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) were analyzed to identify and map minerals, vegetation groups, and volatiles (water and snow) in support of geologic studies of the Bodie Hills, Sweetwater Mountains, and Wassuk Range, California/Nevada. Digital mineral and vegetation mapping results are presented in both portable document format (PDF) and ERDAS Imagine format (.img). The ERDAS-format files are suitable for integration with other geospatial data in Geographic Information Systems (GIS) such as ArcGIS. The ERDAS files showing occurrence of 1) iron-bearing minerals, vegetation, and water, and 2) clay, sulfate, mica, carbonate, Mg-OH, and hydrous quartz minerals have been attributed according to identified material, so that the material detected in a pixel can be queried with the interactive attribute identification tools of GIS and image processing software packages (for example, the Identify Tool of ArcMap and the Inquire Cursor Tool of ERDAS Imagine). All raster data have been orthorectified to the Universal Transverse Mercator (UTM) projection using a projective transform with ground-control points selected from orthorectified Landsat Thematic Mapper data and a digital elevation model from the U.S. Geological Survey (USGS) National Elevation Dataset (1/3 arc second, 10 m resolution). Metadata compliant with Federal Geographic Data Committee (FGDC) standards for all ERDAS-format files have been included, and contain important information regarding geographic coordinate systems, attributes, and cross-references. Documentation regarding spectral analysis methodologies employed to make the maps is included in these cross-references.

Scientific Investigations Map↗

USGS1954

The East Slope No. 2 uranium prospect, Piute County, Utah

The secondary uranium minerals autunite, metatorbernite, uranophane(?), and schroeckingerite occur in altered hornfels at the East Slope No. 9. uranium prospect. The deposit, in sec. 6, T. 9.7 S., R. 3 W., Piute County, Utah, is about 1 mile west of the Bullion Monarch mine which is in the central producing area of the Marysvale uranium district. Hornfels, formed by contact metamorphism of rocks of the Bullion Canyon volcanics borderhug the margin of a quartz monzonite stock, is in fault contact with the later Mount Belknap rhyolite. The hornfels was intensely altered by hydrothermal solutions in pre-Mount Belknap time. Hematite-alunite-quartz-kaolinite rock, the most completely altered hornfels, is surrounded by orange to white argillized hornfels containing beidellite-montmorillonite clay, and secondary uranium minerals. The secondary uranium minerals probably have been derived from pitchblende, the primary ore mineral in other deposits of the Marysvale area. The two uranium-rich zones, 4 feet ad 5 feet thick, have been traced on the surface for 60 feet and 110 feet, respectively. Channel samples from these zones contained as much as 0.047 percent uranium. The deposit is significant because of its position outside the central producing area and because of the association of uranium minerals with alunitic rock in hydrothermally altered hornfels of volcanic rocks of early Tertiary age.

Circular↗

USGS2009

The role of reaction affinity and secondary minerals in regulating chemical weathering rates at the Santa Cruz Soil Chronosequence, California

In order to explore the reasons for the apparent discrepancy between laboratory and field weathering rates and to determine the extent to which weathering rates are controlled by the approach to thermodynamic equilibrium, secondary mineral precipitation, and flow rates, a multicomponent reactive transport model (CrunchFlow) was used to interpret soil profile development and mineral precipitation and dissolution rates at the 226 ka Marine Terrace Chronosequence near Santa Cruz, CA. Aqueous compositions, fluid chemistry, transport, and mineral abundances are well characterized [White A. F., Schulz M. S., Vivit D. V., Blum A., Stonestrom D. A. and Anderson S. P. (2008) Chemical weathering of a Marine Terrace Chronosequence, Santa Cruz, California. I: interpreting the long-term controls on chemical weathering based on spatial and temporal element and mineral distributions. Geochim. Cosmochim. Acta 72 (1), 36-68] and were used to constrain the reaction rates for the weathering and precipitating minerals in the reactive transport modeling. When primary mineral weathering rates are calculated with either of two experimentally determined rate constants, the nonlinear, parallel rate law formulation of Hellmann and Tisserand [Hellmann R. and Tisserand D. (2006) Dissolution kinetics as a function of the Gibbs free energy of reaction: An experimental study based on albite feldspar. Geochim. Cosmochim. Acta 70 (2), 364-383] or the aluminum inhibition model proposed by Oelkers et al. [Oelkers E. H., Schott J. and Devidal J. L. (1994) The effect of aluminum, pH, and chemical affinity on the rates of aluminosilicate dissolution reactions. Geochim. Cosmochim. Acta 58 (9), 2011-2024], modeling results are consistent with field-scale observations when independently constrained clay precipitation rates are accounted for. Experimental and field rates, therefore, can be reconciled at the Santa Cruz site. Additionally, observed maximum clay abundances in the argillic horizons occur at the depth and time where the reaction fronts of the primary minerals overlap. The modeling indicates that the argillic horizon at Santa Cruz can be explained almost entirely by weathering of primary minerals and in situ clay precipitation accompanied by undersaturation of kaolinite at the top of the profile. The rate constant for kaolinite precipitation was also determined based on model simulations of mineral abundances and dissolved Al, SiO 2 (aq) and pH in pore waters. Changes in the rate of kaolinite precipitation or the flow rate do not affect the gradient of the primary mineral weathering profiles, but instead control the rate of propagation of the primary mineral weathering fronts and thus total mass removed from the weathering profile. Our analysis suggests that secondary clay precipitation is as important as aqueous transport in governing the amount of dissolution that occurs within a profile because clay minerals exert a strong control over the reaction affinity of the dissolving primary minerals. The modeling also indicates that the weathering advance rate and the total mass of mineral dissolved is controlled by the thermodynamic saturation of the primary dissolving phases plagioclase and K-feldspar, as is evident from the difference in propagation rates of the reaction fronts for the two minerals despite their very similar kinetic rate laws. ?? 2009 Elsevier Ltd.

Geochimica et Cosmochimica Acta↗

USGS1945

Manganese content of the Shady dolomite in Bumpass Cove, Tennessee

The Shady dolomite in Bumpass Cove, Tennessee, contains deposits of hydrothermal sulphide minerals, and its residual clay contains oxidized manganese deposits. New chemical evidence bearing on the source of this manganese is presented.Chemical analyses of isolated components of sulphide-bearing dolomite show that the percentage of manganese is highest in country-rock dolomite unaffected by hydrothermal action, and that the manganese is present as carbonate. Manganese determinations on samples from a drill hole show that 43 feet of beds, about 100 feet above the base of the Shady dolomite, average 0.6 per cent manganese oxide, and that adjacent beds carry smaller amounts. Manganese carbonate, deposited with the original carbonate rock, is therefore considered to be the source of the manganese deposits of Bumpass Cove

Tennessee↗

USGS1969

Micromineralogy of silver-bearing sphalerite from Flat River, Missouri

Detailed mineralogical and chemical study of sphalerite-rich lead ores from Flat River, Mo., confirms the presence of anomalous amounts of silver in the sphalerite. Although silver is closely associated with chlorine and no silver sulfide minerals were identified, geochemical considerations indicate the silver may be in the form of discrete submicron-size grains of sulfide rather than chloride. However, the close correlation between abundance variations in silver, chlorine, cadmium, iron, and minor lead suggests the possible existence of submicron-size grains of a complex chloride or oxychloride. Results from detailed chemical study of sphalerite show: (1) chlorine is present in areas containing silver and changes in abundance of both elements are similar; (2) the mole ratio of chlorine to silver varies from approximately 3:1 to 6:1 with an approximate average of 5:1 and the total content of each element varies widely between grains and within the same grain; (3) taking total silver in any analysis and calculating the amount of chlorine required for silver chloride leaves an excess of chlorine; (4) in chlorine-deficient areas the amounts of iron and cadmium substituting for zinc in the sphalerite structure vary widely; and (5) in areas containing chlorine, changes in abundance of iron and cadmium vary directly with that of chlorine. The fine-grained dusty opaque inclusions characterize sphalerite from this area; they were identified as mainly galena with lesser amounts of pyrite and cassiterite. Galena is silver-free (<0.02 weight percent Ag) and is essentially pure lead sulfide. Other sulfides identified include pyrite, a cobalt-nickel-iron sulfide of composition Co (sub 0.55) Ni (sub 0.25) Fe (sub 0.20) S (sub 2.00), and an iron-cobalt-nickel sulfide containing 22-28 weight percent Fe, 10-15 weight percent Co, and 3-5 weight percent Ni. Anomalous amounts of tin present as cassiterite are associated with the gangue minerals quartz, potash feldspar, a kaolinite-type clay, and trace amounts of cuprite. Carbonate gangue minerals include calcite, dolomite, ankerite, magnesite, and minor amounts of cerussite. Chemical analyses were made of many minerals and physical and textural relationships examined.

Missouri↗

USGS1953

Geology of the Plumtree area, Spruce Pine district, North Carolina

This report describes the results of study and geologic mapping (1:12,000) in the 70-square-mile Plumtree area in the northeastern part of the Spruce Pine pegmatite district, on the Blue Ridge upland in western North Carolina. The district has been the chief domestic source of feldspar and sheet mica. The mining belt just west of the Blue Ridge Front trends northeast and is 25 miles long and 10 miles wide. The center of the Plumtree area lies 10 miles northeast of Spruce Pine pegmatite district, on the Blue Ridge upland in western North Carolina. The district has been the chief domestic source of feldspar and sheet mica. The mining belt just west of the Blue Ridge Front trends northeast and is 25 miles long and 10 miles wide. The center of the Plumtree area lies 10 miles northeast of Spruce Pine and includes parts of Mitchell and Avery Counties shown on the portions of the 7.5-minute Spruce Pine, Linville Falls, Newland, North Carolina, and Carvers Gap, North Carolina and Tennessee quadrangle. The topography varies from rugged mountains to rounded or flat topped hills near the entrenched, meandering master streams. Old erosion surfaces are approximately 600,1,100, 1,500, and 2,500 feet above the present master stream level. The area is in late youth or early maturity after rejuvenation.. The regionally metamorphosed rocks of the amophibolite facies form three mappable units: mica gneiss, mica schist, and hornblende rock. These rocks, perhaps of Precambrian age, are intimately interlayered with thicknesses of the individual layers ranging from less than one inch to several tons of feet. Field relationships and chemical data suggest that the mica (Carolina-type) rocks were derived from sandstones, graywackes, and shales and that the hornblende-rich (Roan-type) layers were derived from impure carbonate rocks. The igneous rocks include alaskite and associated pegmatite of early Paleozoic age (?), dunite and associated soapstone of a prepegmatite age, and a few diabasic dikes of post-pegmatite age (Triassic?). The alaskite and pegmatite have similar bulk compositions, notably low in iron (0.3 percent). The major constituents in order of decreasing abundance are plagioclase, perthitic microcline, quartz, and muncovite. All of these minerals, as well as clay deposits derived from the weathering of alaskite under old terraces, have economic value. The zoned pegmatites contain fewer zones which are less complex mineralogically than those in the pegmatites of many other areas. These essentially unmetamorphosed bodies were intruded approximately at the peak of the regional metamorphism. Their emplacement was controlled by local structure and rock type. The source of this igneous material may have been the mobilized portions of the Cranberry gneiss which underlies the area. The dunite bodies were intruded early in the metamorphic cycle. The bodies are commonly zoned: from the wall rock inwards (1) talc-antrophyllite-serpentine fringe, (3) serpentinized dunite, (3) granular olivine core. Dunite, chromite, vermiculite, and anthophyllite are the major economic commodities. Extensive hydrothermal alteration of dunite bodies produced soapstone. The area is the northeast end of a southwest plunging synclinorium about 20 miles wide with the steeper limb on the northwest side. There are three structural zones: zone I on the northwest is characterized by the northeast-trending isoclinal folds with steep southeast dips; zone II on the southwest includes an area of rocks with low and variable dip; zone III is the complex central core. In the extreme northeast zones I and II have an indistinct boundary where they coalesce along the rim of the synclinorium. Six stratigraphic units are exposed totaling approximately 10,500 feet of metamorphic rocks. Small scale structural features include a foliation, and a lineation in the planes of the foliation. Minor folding reflects the trends of the major structures. There are randomly orient

Open-File Report↗

USGS1981

Sediment parameters for a fine-grained sediment deposit on the southeastern New England continental shelf

An area of fine-grained sediments south of Martha's Vineyard, Massachusetts, has been interpreted as a contemporary deposit. Textural analysis of cores from this area indicates that the deposit consists of sandy to clayey silts overlying a well sorted relict sand. The maximum thickness of the fine sediments is about 6 meters as determined from a core near the center of this deposit. The mineralogy of the <2 um size fraction is similar in both the fine sediments of the contemporary deposit and the underlying coarse sands. The assemblage consists of about 60% illite, 20% chlorite, and 10% kaolinite with minor amounts of mixed-layered clay and smectites. Heavy mineral analysis from a core near the center of the deposit reveals that opaque minerals, framboidal pyrite, muscovite, hornblende, garnet, and tourmaline constitute over 65% of the total downcore assemblage. Pyrite concentrations vary widely at some intervals and may reflect areas of micro-reducing conditions within the core or changes in source area with time. A persistent mica content indicates the presence of a low-energy environment throughout the depositional history of these fine sediments. Downcore organic carbon concentrations are generally uniform in the fine sediments and average about 1.5 percent. Surficial concentration from a core near the center of this feature is about 10 times greater than concentrations for coarse-grained sands on the surrounding shelf.

New England continental shelf↗

USGS1955

Geology and ground-water resources of Webster County, Iowa

Webster County, comprising an area of 718 square miles just northwest of the center of Iowa, had a population of 44,241 in 1950, with 25,115 in Fort Dodge, the principal city. Some 94.4 percent of the county is in farm land; corn is the principal crop and is used in the raising of hogs and cattle, an important occupation in this part of the country. Mineral products include gypsum, clay, coal, sand, gravel and limestone. The mean annual precipitation at Fort Dodge is 31.21 inches, of which more than 3 inches normally occurs during each of the months May, June, July, August, and September. The average number of growing days is 150. The warmest month generally is July; during December, January, and February the average temperature normally is below freezing. The upland area, comprising over 80 percent of the county, is mostly a gently undulating, slightly eroded glacial-drift plain. Morainal hills of low relief occur in the extreme southern and northern parts of the county. The Des Moines River flows through the county from north to south and, together with its tributaries, drains the entire county except the southwestern part, which is tributary to the Raccoon River. The Des Moines River has cut a deep, narrow valley about 90 feet below the upland in the northern part of the county and about 220 feet below the upland in the southern part. The tributary streams commonly have shallow valleys more than a few miles back from the Des Moines River. Glacial deposits of Pleistocene age, ranging in thickness from 50 feet in the north to 175 feet in the south, mantle the indurated rocks over all the upland area, but indurated rocks ranging in age from Mississippian to Cretaceous are exposed in places along the valleys of the Des Moines River and its tributaries.

Iowa↗

USGS2016

Aptian ‘Shale Gas’ Prospectivity in the Downdip Mississippi Interior Salt Basin, Gulf Coast, USA

This study evaluates regional ‘shale gas’ prospectivity of the Aptian section (primarily Pine Island Shale) in the downdip Mississippi Salt Basin (MSB). Previous work by the U.S. Geological Survey estimated a mean undiscovered gas resource of 8.8 trillion cubic feet (TCF) in the chronostratigraphic-equivalent Pearsall Formation in the Maverick Basin of south Texas, where industry has established a moderately successful horizontal gas and liquids play. Wells penetrating the downdip MSB Aptian section at depths of 12,000-15,000 ft were used to correlate formation tops in a 15-well cross-section extending about 200 miles (mi) east-southeastward from Adams Co. to Jackson Co. Legacy cuttings from these wells were analyzed for thermal maturity and source rock quality. Bitumen reflectance (n=53) increases with increasing present-day burial depth in the east-central study area from 1.0% to 1.7%. As the Aptian section shallows in Adams Co. to the west, bitumen Ro values are higher (1.7-2.0%), either from relatively greater heat flux or greater mid-Cenomanian uplift and erosion in this area. Total organic carbon (TOC) content ranges 0.01-1.21 and averages 0.5 wt.% (n=51); pyrolysis output (S2; n=51) averages 0.40 mg HC/g rock, indicating little present-day hydrocarbon-generative potential. Bitumen reflectance is preferred as a thermal maturity parameter as Tmax values are unreliable. Normalized X-ray diffraction (XRD) mineral analyses (n=26) indicate high average clay abundance (53 wt.%) relative to quartz (29%) and carbonate (18%). Mineral content shows a spatial relationship to an Appalachian orogen clastic sediment source, with proximal high clay and quartz and distal high carbonate content. Clastic influx from the Appalachian orogen is confirmed by detrital zircon U-Pb ages with dominant Grenville and Paleozoic components [105 ages from a Rodessa sandstone and 112 ages from a Paluxy (Albian) sandstone]. Preliminary information from fluid inclusion microthermometry (41 aqueous measurements from calcite cements in one argillaceous James Limestone sample) indicates homogenization temperatures (Th) of 120-135°C, consistent with present-day bottom-hole conditions and measured bitumen Ro values towards the western end of the MSB. Downdip in the central MSB, microthermometry (26 aqueous measurements from quartz dust rims in one Paluxy sandstone sample) and measured bitumen Ro values indicate maximum temperatures may have been significantly higher (~25°C) than present-day conditions. High inclusion salinities (15-25 wt.% salt) at both locations suggest interaction of pore fluids with evaporites. Mercury injection capillary pressure (MICP) analyses (n=3) indicate porosity ranges 1.3-2.1% and permeability 0.006-0.02 µD for Pine Island and Rodessa shales. Overall, results from this work indicate generally poor ‘shale gas’ prospectivity compared to other shale reservoirs based primarily on depth, low organic content, low porosity, and high clay content. However, thickness and thermal maturity are appropriate, moderate reservoir pressures are present, and petroleum systems modelling by others has indicated high undiscovered gas potential for the basin as a whole.

Conference Paper↗