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At least 487 records · Page 27Linked to original sources

Groundwater-quality data and regional trends in the Virginia Coastal Plain, 1906-2007

A newly developed regional perspective of the hydrogeology of the Virginia Coastal Plain incorporates updated information on groundwater quality in the area. Local-scale groundwater-quality information is provided by a comprehensive dataset compiled from multiple Federal and State agency databases. Groundwater-sample chemical-constituent values and related data are presented in tables, summaries, location maps, and discussions of data quality and limitations. Spatial trends in groundwater quality and related processes at the regional scale are determined from interpretive analyses of the sample data. Major ions that dominate the chemical composition of groundwater in the deep Piney Point, Aquia, and Potomac aquifers evolve eastward and with depth from (1) 'hard' water, dominated by calcium and magnesium cations and bicarbonate and carbonate anions, to (2) 'soft' water, dominated by sodium and potassium cations and bicarbonate and carbonate anions, and lastly to (3) 'salty' water, dominated by sodium and potassium cations and chloride anions. Chemical weathering of subsurface sediments is followed by ion exchange by clay and glauconite, and subsequently by mixing with seawater along the saltwater-transition zone. The chemical composition of groundwater in the shallower surficial and Yorktown-Eastover aquifers, and in basement bedrock along the Fall Zone, is more variable as a result of short flow paths between closely located recharge and discharge areas and possibly some solutes originating from human sources. The saltwater-transition zone is generally broad and landward-dipping, based on groundwater chloride concentrations that increase eastward and with depth. The configuration is convoluted across the Chesapeake Bay impact crater, however, where it is warped and mounded along zones having vertically inverted chloride concentrations that decrease with depth. Fresh groundwater has flushed seawater from subsurface sediments preferentially around the impact crater as a result of broad contrasts between sediment permeabilities. Paths of differential flushing are also focused along the inverted zones, which follow stratigraphic and structural trends southeastward into North Carolina and northeastward beneath the chloride mound across the outer impact crater. Brine within the inner impact crater has probably remained unflushed. Regional movement of the saltwater-transition zone takes place over geologic time scales. Localized movement has been induced by groundwater withdrawal, mostly along shallow parts of the saltwater-transition zone. Short-term episodic withdrawals result in repeated cycles of upconing and downconing of saltwater, which are superimposed on longer-term lateral saltwater intrusion. Effective monitoring for saltwater intrusion needs to address multiple and complexly distributed areas of potential intrusion that vary over time. A broad belt of large groundwater fluoride concentrations underlies the city of Suffolk, and thins and tapers northward. Fluoride in groundwater probably originates by desorbtion from phosphatic sedimentary material. The high fluoride belt possibly was formed by initial adsorbtion of fluoride onto sediment oxyhydroxides, followed by desorbtion along the leading edge of the advancing saltwater-transition zone. Large groundwater iron and manganese concentrations are most common to the west along the Fall Zone, across part of the saltwater-transition zone and eastward, and within shallow groundwater far to the east. Iron and manganese initially produced by mineral dissolution along the Fall Zone are adsorbed eastward and with depth by clay and glauconite, and subsequently desorbed along the leading edge of the advancing saltwater-transition zone. Iron and manganese in shallow groundwater far to the east are produced by reaction of sediment organic matter with oxyhydroxides. Large groundwater nitrate and ammonium concentrations are mostly limited to shallow depths. Most nitrate a

Professional Paper↗

Controls on the Karaha-Telaga Bodas geothermal reservoir, Indonesia

Karaha-Telaga Bodas is a partially vapor-dominated, fracture-controlled geothermal system located adjacent to Galunggung Volcano in western Java, Indonesia. The geothermal system consists of: (1) a caprock, ranging from several hundred to 1600 m in thickness, and characterized by a steep, conductive temperature gradient and low permeability; (2) an underlying vapor-dominated zone that extends below sea level; and (3) a deep liquid-dominated zone with measured temperatures up to 353 ??C. Heat is provided by a tabular granodiorite stock encountered at about 3 km depth. A structural analysis of the geothermal system shows that the effective base of the reservoir is controlled either by the boundary between brittle and ductile deformational regimes or by the closure and collapse of fractures within volcanic rocks located above the brittle/ductile transition. The base of the caprock is determined by the distribution of initially low-permeability lithologies above the reservoir; the extent of pervasive clay alteration that has significantly reduced primary rock permeabilities; the distribution of secondary minerals deposited by descending waters; and, locally, by a downward change from a strike-slip to an extensional stress regime. Fluid-producing zones are controlled by both matrix and fracture permeabilities. High matrix permeabilities are associated with lacustrine, pyroclastic, and epiclastic deposits. Productive fractures are those showing the greatest tendency to slip and dilate under the present-day stress conditions. Although the reservoir appears to be in pressure communication across its length, fluid, and gas chemistries vary laterally, suggesting the presence of isolated convection cells. ?? 2006 CNR.

Geothermics↗

Composition of aeolian dust in natural traps on isolated surfaces of the central Mojave Desert - Insights to mixing, sources, and nutrient inputs

The recognition and characterization of aeolian dust in soil contribute to a better understanding of landscape and ecosystem dynamics of drylands. Results of this study show that recently deposited dust, sampled in isolated, mostly high-ground settings, is chemically and mineralogically similar on varied geologic substrates over a large area (15 000 km2) in the Mojave Desert. The silt-plus-clay fraction (fines) on these isolated surfaces is closely alike in magnetic-mineral composition, in contrast to greatly dissimilar magnetic compositions of rock surfaces of vastly different lithologies, on which the fines have accumulated. The fines, thus, are predominantly deposited dust. The amounts of potential nutrients in the sampled dust are much more uniform than might be provided by direct, local weathering of bedrock or by dust locally derived from nearby weathered products. The compositional similarity of the dust on these surfaces is interpreted to result from mixing of fines in the atmosphere as well as in fluvial, alluvial, and lacustrine depositional settings prior to dust emission.

Journal of Arid Environments↗

Figurines, flint clay sourcing, the Ozark Highlands, and Cahokian acquisition

At the pinnacle of Eastern Woodlands’ prehistoric cultural development, Cahokia has been interpreted as a political and economic power participating in prestige-goods exchanges and trade networks stretching from the Great Plains to the South Atlantic. Among the more spectacular of the Cahokian elite artifacts were stone pipes and figurines made from a distinctive red stone previously identified as Arkansas bauxite. In this research, we used a combination of X-ray diffraction, sequential acid dissolution, and inductively coupled plasma analyses to establish the source of the raw material used in the manufacture of the red figurines and pipes that epitomize the Cahokian-style. Our research demonstrates that these objects were made of locally available flint clays. This finding, in conjunction with other evidence, indicate Cahokian exploitation of many mineral and stone resources focuses on the northern Ozark Highlands to the exclusion of other areas. These findings indicate that we must reassess the direction, extent, and role of Cahokian external contacts and trade in elite goods.

Illinois↗

A note on the frictional strength of laumontite from Cajon Pass, California

Laumontite mineralization is pervasive in joints and shear zones encountered in the Cajon Pass drillhole in southern California. In order to determine whether a gouge composed of this hydrated mineral affects shear strength in a manner similar to low-strength, clay-rich fault gouges, frictional sliding experiments were performed under dry, saturated and high pore pressure conditions at effective pressures up to 450 MPa. Coefficients of friction ranged between 0.66 and 0.84, consistent with most crustal rocks and well above the values typical of clay-rich San Andreas fault gouges. Saturation state had no effect on strength or sliding stability. These results suggest that the presence of laumontite in shear zones at Cajon Pass will not affect the shear strength of the rock in a way that can account for the inferred low ambient shear stresses. -Authors

Geophysical Research Letters↗

Localized sulfate-reducing zones in a coastal plain aquifer

High concentrations of dissolved iron in ground water of coastal plain or alluvial aquifers contribute to the biofouling of public supply wells for which treatment and remediation is costly. Many of these aquifers, however, contain zones in which microbial sulfate reduction and the associated precipitation of iron-sulfide minerals decreases iron mobility. The principal water- bearing aquifer (Magothy Aquifer of Cretaceous age) hi Suffolk County, New York, contains localized sulfate-redudng zones hi and near lignite deposits, which generally are associated with clay lenses. Microbial analyses of core samples amended with [ 14 C]-acetate indicate that microbial sulfate reduction is the predominant terminal-electron-accepting process (TEAP) in poorly permeable, lignite-rich sediments at shallow depths and near the ground water divide. The sulfate-reducing zones are characterized by abundant lignite and iron-sulfide minerals, low concentrations of Fe(III) oxyhydroxides, and by proximity to clay lenses that contain pore water with relatively high concentrations of sulfate and dissolved organic carbon. The low permeability of these zones and, hence, the long residence time of ground water within them, permit the preservation and (or) allow the formation of iron-sulfide minerals, including pyrite and marcasite. Both sulfate-reducing bacteria (SRB) and iron-reducing bacteria (IRB) are present beneath and beyond the shallow sulfate-reducing zones. A unique Fe(HI)-reducing organism, MD-612, was found in core sediments from a depth of 187 m near the southern shore of Long Island. The distribution of poorly permeable, lignite-rich, sulfate-reducing zones with decreased iron concentration is varied within the principal aquifer and accounts for the observed distribution of dissolved sulfate, iron, and iron suit Ides in the aquifer. Locating such zones for the placement of production wells would be difficult, however, because these zones are of limited aerial extent.

Ground Water↗

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

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

Colorado↗

Stratigraphic framework and heavy minerals of the continental shelf of Onslow and Long Bays, North Carolina

One hundred fourteen vibracores from the Atlantic continental shelf offshore of southeastern North Carolina were opened, described, and processed over several contract years (years 6-9) of the Minerals Management Service-Association of American State Geologists Continental Margins program. Reports for years 9 and 10 of the program compiled the results of the work and assembled the data for release as an interactive CD-ROM report, respectively. The continental shelf of Onslow and Long Bays consists predominantly of outcropping Cretaceous through late Tertiary geologic units. Nearshore these units are covered and incised by late Tertiary and Quaternary units. From oldest to youngest, formally recognized geologic units mapped as part of this study are the Late Cretaceous Peedee Formation-a muddy, fine- to medium-grained quartz sand with trace amounts of glauconite and phosphate; the Paleocene Beaufort Formation-a muddy, fine- to medium-grained glauconitic quartz sand with locally occurring turritelid-mold biosparrudite; the middle Eocene Castle Hayne Formation-a sandy bryozoan biomicrudite and biosparrudite; the Oligocene River Bend Formation-a sandy molluscan-mold biosparrudite; and the Miocene Pungo River Formation-a medium-grained, poorly sorted slightly shelly phosphatic sand. Informal units include a very widespread, unnamed fine- to very fine grained, well-sorted, dolomitic muddy quartz sand that is biostratigraphically equivalent to the Oligocene River Bend Formation; several large valley-fill lithosomes composed of biomicrudite, biomicrite, and biosparrudite of Plio/Pleistocene age; muddy, shelly sands and silty clays of Pliocene, Pleistocene, or mixed Plio/Pleistocene age; and loose, slightly shelly, medium- to coarse-grained sands assigned a Holocene age. Heavy minerals (SG > 2.96) comprise an average of 0.54 wt% (on a bulk-sample basis) of the sediments in 306 samples derived from the 114 vibracores. Heavy-mineral content ranges from <0.01 to 3.69 wt%. The economic heavy mineral content (EHM = ilmenite + zircon + rutile + aluminosilicates + leucoxene [altered ilmenite] + monazite) of the bulk samples averages 0.26 wt% in a range of <0.01-1.70 wt%. As a percentage of the heavy-mineral concentrate, the average EHM value is 45.78% in a range of 0.27-68.60%. The distribution of heavy minerals offshore of southeastern North Carolina is controlled by the lithostratigraphic framework. The unnamed Oligocene sand unit has the highest heavy-mineral content, averaging 0.86 wt% on a bulk-sample basis. The remaining geologic units and their heavy-mineral content (in decreasing order of abundance) are Beaufort (0.64%), Holocene sand (0.60%), Plio-Pleistocene muddy sand and silty clay (0.59%), Peedee (0.42%), River Bend (0.34%), Plio-Pleistocene carbonate (0.12%), and Castle Hayne (0.08%). The heavy-mineral assemblage is fairly consistent throughout the different units. Significantly smaller percentages of heavy minerals correlate with increased amounts of CaCO 3 in the sediments. The sediments analyzed in this study have significantly lower overall heavy-mineral content, as well as lower EHM content than sediments that are known to host commercially important heavy-mineral deposits in the southeastern United States. The potential for economic deposits of heavy minerals in the area of this study, therefore, appears to be limited.

Marine Georesources and Geotechnology↗

Preliminary study on the mode of occurrence of arsenic in high arsenic coals from southwest Guizhou Province

Coal samples from high arsenic coal areas have been analyzed by electron micropbe analyzer (EMPA), scanning electron microscopy with an energy dispersive X-ray analyzer (SEM-EDX), X-ray diffinction analysis (XRD), low temperature ashing (LTA), transmission electron microscopy (TEM), X-ray absorption fine structure (XAFS), instnunent neutron activation analysis (INAA) and wet chemical analysis. Although some As-bearing minerals such as pyrite, arsenopyrite, realgar (?), As-bearing sulfate, and As-bearing clays are found in the high arsenic coals, their contents do not account for the abundance of arsenic in the some coals. Analysis of the coal indicates that arsenic exists mainly in the form of A s 5+ and A s 3+ , combined with compounds in the organic matrix. The occurrence of such exceptionally high arsenic contents in coal and the fact that the arsenic is dominantly organically associated are unique observations. The modes of occurrence of arsenic in high As-coals are discussed.

Science in China, Series D: Earth Sciences↗

Tertiary gold-bearing channel gravel in northern Nevada County, California

The remains of a huge Tertiary gravel-filled channel lie in the area between the South and Middle Yuba Rivers in northern Nevada County, Calif. The deposits in this channel were the site of some of the most productive hydraulic gold mines in California between the 1850's and 1884. The gravel occupies a major channel and parts of several tributaries that in Tertiary time cut into a surface of Paleozoic and Mesozoic igneous and metamorphic rocks. The gravel is partly covered by the remains of an extensive sheet of volcanic rocks, but it crops out along the broad crest of the ridge between the canyons of the South and Middle Yuba Rivers. The lower parts of the gravel deposits generally carry the highest values of placer gold. Traditionally, the richest deposits of all are found in the so-called blue gravel, which, when present, lies just above the bedrock and consists of a very coarse, poorly sorted mixture of cobbles, pebbles, sand, and clay. It is unoxidized, and, at least locally, contains appreciable quantities of secondary sulfide minerals, chiefly pyrite. Information in drill logs from private sources indicates that a 2-mile stretch of the channel near North Columbia contains over half a million ounces of gold dispersed through about 22 million cubic yards of gravel at a grade .averaging about 81 cents per cubic yard. The deposit is buried at depths ranging from 100 to 400 feet. Several geophysical methods have been tested for their feasibility in determining the configuration of the buried bedrock surface, in delineating channel gravel buried under volcanic rocks, and in identifying concentrations of heavy minerals within the gravel. Although the data have not yet been completely processed, preliminary conclusions indicate that some methods may be quite useful. A combination of seismic-refraction and gravity methods was used to determine the depth and configuration of the bottom of the channel to an accuracy within 10 percent as checked by the drill holes. Seismic-refraction methods have identified depressions which are in the bedrock surface, below volcanic rocks, and which may be occupied by gravels. Seismic methods, however, cannot actually recognize the presence of low-velocity gravels beneath the higher velocity volcanic rocks. Electromagnetic methods, supplemented in part by induced-polarization methods, show promise of being able to recognize and trace blue gravel buried less than 200 feet deep. A broad vague magnetic anomaly across the channel suggests that more precise magnetic studies might delineate concentrations of magnetic material. The usefulness of resistivity methods appears from this study to be quite restricted because of irregular topography and the variable conductivity of layers within the gravel.

Circular↗

Maps showing mines, quarries, oil and gas activity, and sample localities in and near the Sipsey Wilderness and additions, Lawrence and Winston counties, Alabama

The U.S. Bureau of Mines conducted a field reconnaissance of Sipsey Wilderness in the fall of 1978 and of the roadless areas in the spring and summer of 1979. Mines, quarries, prospects, exposures, and drill sites in and near the study area were examined. Fifty-three samples were collected during the field work; sample localities are shown in figure 3. Analyses and preliminary test results for all limestone, clay and shale, sandstone, and coal samples were reported by Mory and others (1981). Mineral resource potential of the Sipsey Wilderness and additions is reported by Schweinfurth and others (1982). No mining activities are being conducted in the study area at present. Previous mining has been limited to small-scale production of limestone and coal. Two oil and gas test holes have been drilled inside the study area.

Alabama↗

Geologic Map of the Kings Mountain and Grover Quadrangles, Cleveland and Gaston Counties, North Carolina, and Cherokee and York Counties, South Carolina

This geologic map of the Kings Mountain and Grover 7.5-min quadrangles, N.C.-S.C., straddles a regional geological boundary between the Inner Piedmont and Carolina terranes. The Kings Mountain sequence (informal name) on the western flank of the Carolina terrane in this area includes the Neoproterozoic Battleground and Blacksburg Formations. The Battleground Formation has a lower part consisting of metavolcanic rocks and interlayered schist and an upper part consisting of quartz-sericite phyllite and schist interlayered with quartz-pebble metaconglomerate, aluminous quartzite, micaceous quartzite, manganiferous rock, and metavolcanic rocks. The Blacks-burg Formation consists of phyllitic metasiltstone interlayered with thinner units of marble, laminated micaceous quartzite, hornblende gneiss, and amphibolite. Layered metamorphic rocks of the Inner Piedmont terrane include muscovite-biotite gneiss, muscovite schist, and amphibolite. The Kings Mountain sequence has been intruded by metatonalite and metatrondhjemite (Neoproterozoic), metagabbro and metadiorite (Paleozoic?), and the High Shoals Granite (Pennsylvanian). Layered metamorphic rocks of the Inner Piedmont in this area have been intruded by the Toluca Granite (Ordovician?), the Cherryville Granite and associated pegmatite (Mississippian), and spodumene pegmatite (Mississippian). Diabase dikes (early Jurassic) are locally present throughout the area. Ductile fault zones of regional scale include the Kings Mountain and Kings Creek shear zones. In this area, the Kings Mountain shear zone forms the boundary between the Inner Piedmont and Carolina terranes, and the Kings Creek shear zone separates the Battleground Formation from the Blacksburg Formation. Structural styles change across the Kings Mountain shear zone from steeply dipping layers, foliations, and folds on the southeast to gently and moderately dipping layers, foliations, and recumbent folds on the northwest. Mineral assemblages in the Kings Mountain sequence show a westward decrease from upper amphibolite facies (sillimanite zone) near the High Shoals Granite in the eastern side of the map area to upper greenschist (epidote-amphibolite) facies in the south-central part of the area near the Kings Mountain shear zone. Amphibolite-facies mineral assemblages in the Inner Piedmont terrane increase in grade from the kyanite zone near the Kings Mountain shear zone to the sillimanite zone in the northwestern part of the map area. Surficial deposits include alluvium in the stream valleys and colluvium along ridges and steep slopes. These quadrangles are unusual in the richness and variety of the mineral deposits that they contain, which include spodumene (lithium), cassiterite (tin), mica, feldspar, silica, clay, marble, kyanite and sillimanite, barite, manganese, sand and gravel, gold, pyrite, and iron.

Scientific Investigations Map↗

Porosity of the Marcellus Shale: A contrast matching small-angle neutron scattering study

Neutron scattering techniques were used to determine the effect of mineral matter on the accessibility of water and toluene to pores in the Devonian Marcellus Shale. Three Marcellus Shale samples, representing quartz-rich, clay-rich, and carbonate-rich facies, were examined using contrast matching small-angle neutron scattering (CM-SANS) at ambient pressure and temperature. Contrast matching compositions of H 2 O, D 2 O and toluene, deuterated toluene were used to probe open and closed pores of these three shale samples. Results show that although the mean pore radius was approximately the same for all three samples, the fractal dimension of the quartz-rich sample was higher than for the clay-rich and carbonate-rich samples, indicating different pore size distributions among the samples. The number density of pores was highest in the clay-rich sample and lowest in the quartz-rich sample. Contrast matching with water and toluene mixtures shows that the accessibility of pores to water and toluene also varied among the samples. In general, water accessed approximately 70–80% of the larger pores (>80 nm radius) in all three samples. At smaller pore sizes (~5–80 nm radius), the fraction of accessible pores decreases. The lowest accessibility to both fluids is at pore throat size of ~25 nm radii with the quartz-rich sample exhibiting lower accessibility than the clay- and carbonate-rich samples. The mechanism for this behaviour is unclear, but because the mineralogy of the three samples varies, it is likely that the inaccessible pores in this size range are associated with organics and not a specific mineral within the samples. At even smaller pore sizes (~<2.5 nm radius), in all samples, the fraction of accessible pores to water increases again to approximately 70–80%. Accessibility to toluene generally follows that of water; however, in the smallest pores (~<2.5 nm radius), accessibility to toluene decreases, especially in the clay-rich sample which contains about 30% more closed pores than the quartz- and carbonate-rich samples. Results from this study show that mineralogy of producing intervals within a shale reservoir can affect accessibility of pores to water and toluene and these mineralogic differences may affect hydrocarbon storage and production and hydraulic fracturing characteristics

International Journal of Coal Geology↗

What's weathering? Mineralogy and field leach studies in mine waste, Leadville and Montezuma mining districts, Colorado

Weathering is important in the development of rock fabrics that control porosity in mine-waste materials, and in turn, porosity affects metal transport through and from mine-waste piles into watersheds. Mine-waste piles are dynamic physical and chemical systems as evidenced by remnant Fe-oxide boxwork structures after sulfide minerals, development of alteration rinds and etch pits on grains, and precipitation of secondary minerals under low temperature conditions. These microscale changes in the mine-waste materials are the result of partial to total dissolution of sulfide and other minerals. Mine-waste materials from the Dinero, Lower Chatauqua, and Saints John sites, Leadville and Montezuma mining districts, Colorado, exhibit rock fabrics that indicate that weathering products, e.g., Fe oxyhydroxides, jarosite, and clays, have been transported in suspension through the waste piles and deposited in voids and as coatings on rock fragments. Microscale characterization of weathered, partially dissolved minerals lends insight into the source of leachable metals in these mine-waste sites. Mineralogic studies show that galena in the Lower Chatauqua waste is enriched in Ag. Qualitative and semiquantitative microanalysis of weathered, altered galena grains from all three sites show that the Ag-bearing galena is more susceptible to dissolution. It is not surprising, then, that solutions experimentally leached from Lower Chatauqua waste are higher in Pb (2310 ppb) compared to leachates from the Dinero (31 ppb) and Saints John (1360 ppb) wastes. The mobility of metals is increased at acidic pH. Using the USGS Field Leach Test protocol, leachate derived from the Dinero waste has a pH of 3 and high concentrations of Al (443 ppb), Fe (441 ppb), and Zn (7970 ppb). Leachate from Sts. John tailings has a pH about 4 and high concentrations of Mn (1520 ppb), Zn (2240 ppb), and Pb (1360 ppb). Leachate from the Lower Chatauqua waste has an intermediate pH of 5, but in addition to the high Pb level already mentioned, it contains high levels of K (1.9 ppm), Mn (6720 ppb), and Zn (1550 ppb). The high concentration of metals, despite the intermediate pH of the leachate, may be explained by acidic microenvironments that exist at the surfaces of sulfide minerals, where sulfur-and iron-oxidizing microbes may flourish. It is at the reactive mineral-oxygen-water interface where metals are released and low-pH sulfate precipitates such as jarosite-beudantite form.

Colorado↗

Crystallographic controls on the frictional behavior of dry and water-saturated sheet structure minerals

We compare the frictional strengths of 17 sheet structure mineral powders, measured under dry and water-saturated conditions, to identify the factors that cause many of them to be relatively weak. The dry coefficient of friction μ ranges upward from 0.2 for graphite, leveling off at 0.8 for margarite, clintonite, gibbsite, kaolinite, and lizardite. The values of μ (dry) correlate directly with calculated (001) interlayer bond strengths of the minerals. This correlation occurs because shear becomes localized along boundary and Riedel shears and the platy minerals in them rotate into alignment with the shear planes. For those gouges with μ (dry) < 0.8, shear occurs by breaking the interlayer bonds to form new cleavage surfaces. Where μ (dry) = 0.8, consistent with Byerlee's law, the interlayer bonds are sufficiently strong that other frictional processes dominate. The transition in dry friction mechanisms corresponds to calculated surface energies of 2–3 J/m 2 . Adding water causes μ to decrease for every mineral tested except graphite. If the minerals are separated into groups with similar crystal structures, μ (wet) increases with increasing interlayer bond strength within each group. This relationship also holds for the swelling clay montmorillonite, whose water-saturated strength is consistent with the strengths of nonswelling clays of similar crystal structure. Water in the saturated gouges forms thin, structured films between the plate surfaces. The polar water molecules are bonded to the plate surfaces in proportion to the mineral's surface energy, and μ (wet) reflects the stresses required to shear through the water films.

Journal of Geophysical Research B: Solid Earth↗

Summary of the mineralogy of the Colorado Plateau uranium ores

In the Colorado Plateau uranium has been produced chiefly from very shallow mines in carnotite ores (oxidized vanadiferous uranium ores) until recent deeper mining penetrated black unoxidized ores in water-saturated rocks and extensive exploration has discovered many deposits of low to nonvanadiferous ores. The uranium ores include a wide range from highly vanadiferous and from as much as one percent to a trace of copper, and contain a small amount of iron and traces of lead, zinc, molybdenum, cobalt, nickel, silver, manganese, and other metals. Recent investigation indicates that the carnotite ores have been derived by progressive oxidation of primary (unoxidized) black ores that contain low-valent uranium and vanadium oxides and silicates. The uranium minerals, uraninite and coffinite, are associated with coalified wood or other carbonaceous material. The vanadium minerals, chiefly montroseite, roscoelite, and other vanadium silicates, occur in the interstices of the sandstone and in siltstone and clay pellets as well as associated with fossil wood. Calcite, dolomite, barite and minor amounts of sulfides, arsenides, and selenides occur in the unoxidized ore. Partially oxidized vanadiferous ore is blue black, purplish brown, or greenish black in contrast to the black or dark gray unoxidized ore. Vanadium combines with uranium to form rauvite. The excess vanadium is present in corvusite, fernandinite, melanovanadite and many other quadrivalent and quinquevalent vanadium minerals as well as in vanadium silicates. Pyrite and part or all of the calcite are replaced by iron oxides and gypsum. In oxidized vanadiferous uranium ores the uranium is fixed in the relatively insoluble minerals carnotite and tyuyamunite, and the excess vanadium commonly combines with one or more of the following: calcium, sodium, potassium, magnesium, aluminum, iron, copper, manganese, or barium, or rarely it forms the hydrated pentoxide. The relatively stable vanadium silicates are little affected by oxidation. The unoxidized nonvanadiferous ores contain uraninite and coffinite in close association with coalified wood and iron and copper sulfides, and traces of many other sulfides, arsenides and selenides. The oxidized nonvanadiferous ores differ from the vanadiferous ores because, in the absence of vanadium to complex the uranium, a great variety of secondary yellow and greenish-yellow uranyl minerals are formed. The uranyl sulfates and carbonates are more common than the oxides, phosphates, arsenates, and silicates. Because the sulfates and carbonates are much less stable that carnotite, the oxidized nonvanadiferous ores occure only as halos around cores of unoxidized ore and do not form large oxidized deposits close to the surface of the ground as carnotite ores. Oxidation has taken place since the lowering of the water table in the present erosion cycle. Because of local structures and the highly lenticular character of the fluviatile host rocks perched water tables and water-saturated lenses of sandstone are common high above the regional water table. Unoxidized ore has been preserved in these water-saturated rocks and the boundary between oxidized and unoxidized ore is very irregular.

Utah↗

Geology of the Anlauf and Drain Quadrangles, Douglas and Lane Counties, Oregon

The Anlauf and Drain quadrangles, Oregon, lie about 20 miles south of the city of Eugene, in Douglas and Lane Counties. They constitute an area of about 435 square miles that includes parts of both the Cascade Range and Coast Range physiographic provinces. A sequence of lower Tertiary sedimentary and volcanic rocks with a maximum thickness of about 20,000 feet is exposed in the area. The oldest part of this sequence is the Umpqua formation of early Eocene age consisting of a lower member of vesicular and amygdaloidal olivine basalt flows, a middle member of water-laid vitric and lapilli crystal tuff, and an upper member of interbedded fissile siltstone and basaltic sandstone which contains a 300-foot tongue of massive to thick-bedded basaltic sandstone near its top. These rocks are predominantly of marine origin, although the general absence of pillow structures which are common in basaltic lavas of equivalent age elsewhere in the Coast Ranges suggests that some of the flows were poured out subaerially. The overlying tuff member, however, contains Foraminifera and in places has a lime content slightly in excess of 10 percent. Mollusca and Foraminifera indicate that the Umpqua formation is of early Eocene age and is a correlative of the Capay formation of California. The Tyee formation of middle Eocene age overlies the Umpqua formation and consists of more than 5,000 feet of rhythmically deposited sandstone and siltstone in beds 2 to 30 feet thick. The basal part of each bed consists of medium- to coarse-grained sandstone that grades upward into fine-grained sand- stone and siltstone. The principal constituents of the sandstone are quartz, partly a1tered feldspar, mica, clay, and fragments of basalt, fine-grained argillaceous rocks, and mica schist. Other detrital minerals include epidote, garnet, blue-green hornblende, tourmaline, and zoisite. The depositional environment of the Tyee formation is poorly known, although the rhythmic-graded bedding suggests turbidity currents. About 500 feet of sandstone and siltstone assigned to the Spencer formation of late Eocene age unconformably overlies the Tyee formation. The Spencer formation, better exposed in the east-central part of the Coast Ranges, contains marine fossils but also has thin impure coal beds, indicative of strand-line accumulation. The sandstone in the Spencer formation is very similar to that in the Tyee formation, from which it was probably derived. The Fisher formation contains about 5,500 feet of nonmarine pyroclastic and volcanic rocks that are related to the volcanic rock sequences of the western Cascade Range. The formation is characterized by a wide variety of rock types, including conglomerate, tuffaceous sandstone and siltstone, vitric and crystal tuff, waterlaid and mudflow breccia, and andesitic lava flows. These rocks gen- erally occur in lenticular beds that have little stratigraphic significance. The rocks apparently accumulated on a plain slightly above sea level that was subjected alternately to fiooding by running water and to desiccation. Fossil leaves from the lowermost part of the Fisher formation are of late Eocene age; the upper part of the formation is of early, and possibly niiddle, Oligocene age. A few exposures of olivine basalt were mapped in the extreme northern part of the Anlauf quadrangle. The flows, more extensively exposed to the north, overlie the Fisher formation, and, therefore, are tentatively considered to be post-Oligocene in age. All these stratigraphic units, but principally the Fisher formation, are cut by dikes, sills, and stocklike bodies of 'porphyritic basalt, diabase, and norite. Contemporaneously with the emplacement of most of these rocks, in late Miocene (?) time, hydrothermal solutions locailly altered the sedimentary and extrusive igneous racks and deposited cinnabar and other sulfide minerals, carbonates, and silica. Three parallel nartheastward-trending

Bulletin↗

Determination of pre-mining geochemical conditions and paleoecology in the Animas River Watershed, Colorado

Determination of the pre-mining geochemical baseline in bed sediments and the paleoecology in a watershed impacted by historical mining activity is of utmost importance in establishing watershed restoration goals. We have approached this problem in the Animas River watershed using geomorphologic mapping methods to identify old pre-mining sediments. A systematic evaluation of possible sites resulted in collection of a large number of samples of pre-mining sediments, overbank sediments, and fluvial tailings deposits from more than 50 sites throughout the watershed. Chemical analysis of individual stratigraphic layers has resulted in a chemical stratigraphy that can be tied to the historical record through geochronological and dendochronological studies at these sites. Preliminary analysis of geochemical data from more than 500 samples from this study, when coupled with both the historical and geochronological record, clearly show that there has been a major impact by historical mining activities on the geochemical record preserved in these fluvial bed sediments. Historical mining activity has resulted in a substantial increase in metals in the very fine sand to clay sized component of the bed sediment of the upper Animas River, and Cement and Mineral Creeks. Enrichment factors for metals in modern bed sediments, relative to the pre-mining sediments, range from a factor of 2 to 6 for arsenic, 4 to more than 10 for cadmium, 2 to more than 10 for lead, 2 to 5 for silver, and 2 to more than 15 for zinc. However, the pre-mining bed sediment geochemical baseline is high relative to crustal abundance levels of many orerelated metals and the watershed would readily be identified as a highly mineralized area suitable for mineral exploration if it had not been disturbed by historical mining activity. We infer from these data that the water chemistry in the streams was less acidic prior to historical mining activity in the watershed. Paleoentologic evidence does not indicate a healthy aquatic habitat in any of the stream reaches investigated above the confluence of the Animas River with Mineral Creek (fig. 1) prior to the impact of historical mining activity. The absence of paleoentologic remains is interpreted to reflect the poor preservation regime of the bed sediment materials sampled. The fluvial sediments sampled in this study represent higher energy environments than are conducive to the preservation of most aquatic organisms including fish remains. We interpret the sedimentological data to indicate that there has been substantial loss of riparian habitat in the upper Animas River above Howardsville as a result of historical mining activity.

Colorado↗