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At least 667 records · Page 37Linked to original sources
USGS1990

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

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

Journal of Contaminant Hydrology↗
USGS1989

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

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

Proceedings of the Ocean Drilling Program: Scienti↗
USGS1998

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

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

Nevada↗
USGS1978

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

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

Alaska↗
USGS2007

Arsenic attenuation by oxidized aquifer sediments in Bangladesh

Recognition of arsenic (As) contamination of shallow fluvio-deltaic aquifers in the Bengal Basin has resulted in increasing exploitation of groundwater from deeper aquifers that generally contain low concentrations of dissolved As. Pumping-induced infiltration of high-As groundwater could eventually cause As concentrations in these aquifers to increase. This study investigates the adsorption capacity for As of sediment from a low-As aquifer near Dhaka, Bangladesh. A shallow, chemically-reducing aquifer at this site extends to a depth of 50 m and has maximum As concentrations in groundwater of 900 μg/L. At depths greater than 50 m, geochemical conditions are more oxidizing and groundwater has < 5 μg/L As. There is no thick layer of clay at this site to inhibit vertical transport of groundwater. Arsenite [As(III)] is the dominant oxidation state in contaminated groundwater; however, data from laboratory batch experiments show that As(III) is oxidized to arsenate [As(V)] by manganese (Mn) minerals that are present in the oxidized sediment. Thus, the long-term viability of the deeper aquifers as a source of water supply is likely to depend on As(V) adsorption. The adsorption capacity of these sediments is a function of the oxidation state of As and the concentration of other solutes that compete for adsorption sites. Arsenite that was not oxidized did adsorb, but to a much lesser extent than As(V). Phosphate (P) caused a substantial decrease in As(V) adsorption. Increasing pH and concentrations of silica (Si) had lesser effects on As(V) adsorption. The effect of bicarbonate (HCO 3 ) on As(V) adsorption was negligible. Equilibrium constants for adsorption of As(V), As(III), P, Si, HCO 3 , and H were determined from the experimental data and a quantitative model developed. Oxidation of As(III) was modeled with a first-order rate constant. This model was used to successfully simulate As(V) adsorption in the presence of multiple competing solutes. Results from these experiments show that oxidized sediments have a substantial but limited capacity for removal of As from groundwater.

Dhaka↗
USGS1962

Tuscaloosa formation in Tennessee

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

Tennessee↗
USGS1995

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

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

Florida↗
USGS1982

Mineral resource potential map of the James River Face Wilderness, Bedford and Rockbridge counties, Virginia

The rocks in the James River Face Wilderness are shales and quartzites that overlie a meta-igneous basement. They are folded into a large southwestward-plunging anticline that is cut off on the east and south by an extensive thrust fault that brings old basement rocks over the younger sedimentary rocks. Geochemical studies of stream sediments, soils, and rocks do not reveal any unusually high metal concentrations, but a large resource of metallurgical-grade quartzite and shale suitable for structural clay products and lightweight aggregate is in the wilderness. Antietam (Erwin) Quartzite has been quarried at three sites in the wilderness as raw material for silicon used in the manufacture of ferrosilicon. Other uses included crushed rock for concrete aggregate, road metal, and railroad ballast, and sand for cement and mortar. Potential uses include ganister for silica brick and specialty sands such as filter and furnace sand. Firing tests on samples of shale from the Harpers (Hampton) Formation show that it could be used for the manufacture of brick and as lightweight aggregate. Of marginal economic interest are heavy-mineral layers in the basal Unicoi (Weverton) Formation.

Virginia↗
USGS1991

Geochemistry of a Tertiary sedimentary phosphate deposit: Baja California Sur, Mexico

The San Gregorio Formation in Baja California Sur, a phosphate-enriched sedimentary unit of late Oligocene to early Miocene age, has been analyzed in two areas (La Purisima and San Hilario) for its chemical composition (major oxides, Cu, Cd, Cr, Co, V, and rare-earth elements - REE) and isotopic composition (??18O and ??13C). A detrital and a marine component were determined from major oxides. The detrital component consists of an unaltered volcanic-ash fraction and a terrigenous clay-silt fraction. The marine component, which accumulated initially as biogenic and hydrogenous material, is now present as opal-A, opal-CT, CaCO3, organic matter, and an authigenic phosphate fraction, mostly pelletal and composed of the carbonate-fluorapatite mineral francolite. The minor elements have been partitioned into these components by assuming a constant composition for the two detrital fractions. The composition of the marine component of minor elements can then be interpreted by assuming that the stoichiometry of the original accumulating organic matter was equal to that of modern plankton. The Cu and Cd contents in the marine component of all rocks require that the seawater-derived fractions of these two metals were supplied to the seafloor solely by organic matter. Enrichments of Cr and V at both sites required an additional marine input. On the basis of their geochemistry in the modern ocean, Cr and V could have precipitated, or been adsorbed, onto settling particles from an O2 minimum zone in which the O2 content was low enough to promote denitrification rather than oxygen respiration. An enrichment of the REE, now within the apatite fraction, resulted from their adsorption onto particulates also in the O2 minimum zone and to the dissolution and alteration of biogenic phases (predominantly silica) within the sediment. Co and Fe2O3 show no enrichment above a detrital contribution. The ??18O-values of apatites from the La Purisima site are heavier than those of apatites from the San Hilario site, whereas the ??13C-values show the opposite trend. One possible interpretation of these variations is that ??18O reflects seawater values and ??13C sediment pore water values. This interpretation suggests that upwelling rates and primary productivity within the water column were greater at La Purisima, an interpretation that is corroborated by a greater abundance of apatite measured in outcrop at La Purisima. The Ce anomalies of the phosphate-enriched samples also differ between the two sites, indicating that they also recorded water masses, similar to the ??18O-values. ?? 1991.

Chemical Geology↗
USGS2012

Occurrence model for volcanogenic beryllium deposits

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

Scientific Investigations Report↗
USGS1945

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

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

New Mexico↗
USGS2014

Comparative mineral chemistry and textures of SAFOD fault gouge and damage-zone rocks

Creep in the San Andreas Fault Observatory at Depth (SAFOD) drillhole is localized to two foliated gouges, the central deforming zone (CDZ) and southwest deforming zone (SDZ). The gouges consist of porphyroclasts of serpentinite and sedimentary rock dispersed in a foliated matrix of Mg-smectite clays that formed as a result of shearing-enhanced reactions between the serpentinite and quartzofeldspathic rocks. The CDZ takes up most of the creep and exhibits differences in mineralogy and texture from the SDZ that are attributable to its higher shearing rate. In addition, a ∼0.2-m-wide sector of the CDZ at its northeastern margin (NE-CDZ) is identical to the SDZ and may represent a gradient in creep rate across the CDZ. The SDZ and NE-CDZ have lower clay contents and larger porphyroclasts than most of the CDZ, and they contain veinlets and strain fringes of calcite in the gouge matrix not seen elsewhere in the CDZ. Matrix clays in the SDZ and NE-CDZ are saponite and corrensite, whereas the rest of the CDZ lacks corrensite. Saponite is younger than corrensite, reflecting clay crystallization under declining temperatures, and clays in the more actively deforming portions of the CDZ have better equilibrated to the lower-temperature conditions.

California↗
USGS1998

Influence of an igneous intrusion on the inorganic geochemistry of a bituminous coal from Pitkin County, Colorado

Although the effects of igneous dikes on the organic matter in coal have been observed at many localities there is virtually no information on the effects of the intrusions of the inorganic constituents in the coal. Such a study may help to elucidate the behavior of trace elements during in situ gasification of coal and may provide insights into the resources potential for coal and coke affected by the intrusion. To determine the effects of an igneous intrusion on the inorganic chemistry of a coal we used a series of 11 samples of coal and natural coke that had been collected at intervals from 3 to 106 cm from a dike that intruded the bituminous Dutch Creek coal in Pitkin, CO. The samples were chemically analyzed for 66 elements. SEM-EDX and X-ray diffraction analysis were performed on selected samples. Volatile elements such as F, Cl, Hg, and Se are not depleted in the samples (coke and coal) nearest the dike that were exposed to the highest temperatures. Their presence in these samples is likely due to secondary enrichment following volatilization of the elements inherent in the coal. Equilibration with ground water may account for the uniform distribution of Na, B, and Cl. High concentrations of Ca, Mg, Fe, Mn, Sr, and CO2 in the coke region are attributed to the reaction of CO and CO2 generated during the coking of the coal with fluids from the intrusion, resulting in the precipitation of carbonates. Similarly, precipitation of sulfide minerals in the coke zone may account for the relatively high concentrations of Ag, Hg, Cu, Zn, and Fe. Most elements are concentrated at the juncture of the fluidized coke and the thermally metamorphosed coal. Many of the elements enriched in this region (for example, Ga, Ge, Mo, Rb, U, La, Ce, Al, K, and Si) may have been adsorbed on either the clays or the organic matter or on both.Although the effects of igneous dikes on the organic matter in coal have been observed at many localities there is virtually no information on the effects of the intrusions on the inorganic constituents in the coal. Such a study may help to elucidate the behavior of trace elements during in situ gasification of coal and may provide insights into the resource potential of coal and coke affected by the intrusion. To determine the effects of an igneous intrusion on the inorganic chemistry of a coal we used a series of 11 samples of coal and natural coke that had been collected at intervals from 3 to 106 cm from a dike that intruded the bituminous Dutch Creek coal in Pitkin, CO. The samples were chemically analyzed for 66 elements. SEM-EDX and X-ray diffraction analysis were performed on selected samples. Volatile elements such as F, Cl, Hg, and Se are not depleted in the samples (coke and coal) nearest the dike that were exposed to the highest temperatures. Their presence in these samples is likely due to secondary enrichment following volatilization of the elements inherent in the coal. Equilibration with ground water may account for the uniform distribution of Na, B, and Cl. High concentrations of Ca, Mg, Fe, Mn, Sr, and CO2 in the coke region are attributed to the reaction of CO and CO2 generated during the coking of the coal with fluids from the intrusion, resulting in the precipitation of carbonates. Similarly, precipitation of sulfide minerals in the coke zone may account for the relatively high concentrations of Ag, Hg, Cu, Zn, and Fe. Most elements are concentrated at the juncture of the fluidized coke and the thermally metamorphosed coal. Many of the elements enriched in this region (for example, Ga, Ge, Mo, Rb, U, La, Ce, Al, K, and Si) may have been adsorbed on either the clays or the organic matter or on both.

International Journal of Coal Geology↗
USGS1989

The Relief Canyon gold deposit, Nevada: A mineralized solution breccia

The Relief Canyon gold deposit in the Humboldt Range of western Nevada is a low-grade, high-tonnage orebody of Tertiary or younger age. The host rocks include limestones of the Triassic Cane Spring Formation, which are overlain by shales of the Triassic Grass Valley Formation. The rocks were folded and metamorphosed to greenschist grade during Jurassic and Cretaceous regional tectonic activity. Mesozoic thrusting may have occurred along the shale-limestone contact, but evidence has been obscured by later hydrothermal activity. The sedimentary rocks were nominally offset along several Late Tertiary normal faults related to uplift of the range.The upper part of the Cane Spring Formation is composed of a poorly sorted breccia composed of limestone clasts with a clay matrix. Irregular pockets within this zone are filled with clay- to pebble-sized fragments derived from the Grass Valley shale. The enclosing limestone beds were tilted moderately to the southwest during Mesozoic deformation, whereas bedding within these pockets is generally horizontal, indicating post-tilting deposition of the sediments. The sediments show graded bedding and other sedimentary features that indicate deposition from flowing water. Thermally mature carbon derived from the limestone is also concentrated in small pockets in the matrix. The breccia unit is likely the product of low-temperature solution brecciation. Ground water dissolved much of the limestone directly beneath the shales, progressively creating irregular cavities and the breccia. Sediments derived from the overlying Grass Valley shale were fiuvially deposited as a matrix to the developing solution breccia.Episodic pulses of hydrothermal fluids were introduced along faults and possibly mixed with the ground water in the breccia zone. Initially, jasperoids formed along the faults, but later hydrothermal pulses introduced gold, silica, and fluorine into both the early jasperoids and the unconsolidated cave-fill sediments to form the orebody. Continued solution-related brecciation chaotically disrupted the gold deposit.Gold, fluorite, pyrite, silver, calcite, and fine-grained silica are the principal hydrothermal minerals in the deposit. Gold was deposited as micron-sized flakes of native gold and rarely as electrum during a relatively late stage of silicification of the jasperoids, the carbon-rich zones, and the clay-rich matrix of the breccia. Fluorite was deposited with and later than the gold in the jasperoids, and it in part replaced the clay-rich breccia matrix. Antimony, arsenic, mercury, and thallium are directly associated with gold in the orebody.The deposit formed at a relatively shallow depth. On the basis of fluid inclusion data, late-stage hydrothermal fluids related to gold and fluorite deposition were extremely dilute and had temperatures near 200 degrees C. The fluid inclusions in fluorite show no evidence for boiling, but porous crackle breccias in the jasperoids suggest that hydrobrecciation took place.

Economic Geology↗
USGS2011

Transient changes in shallow groundwater chemistry during the MSU ZERT CO2 injection experiment

Food-grade CO 2 was injected into a shallow aquifer through a perforated pipe placed horizontally 1–2 m below the water table at the Montana State University Zero Emission Research and Technology (MSU-ZERT) field site at Bozeman, Montana. The possible impact of elevated CO 2 levels on groundwater quality was investigated by analyzing 80 water samples taken before, during, and following CO 2 injection. Field determinations and laboratory analyses showed rapid and systematic changes in pH, alkalinity, and conductance, as well as increases in the aqueous concentrations of trace element species. The geochemical data were first evaluated using principal component analysis (PCA) in order to identify correlations between aqueous species. The PCA findings were then used in formulating a geochemical model to simulate the processes likely to be responsible for the observed increases in the concentrations of dissolved constituents. Modeling was conducted taking into account aqueous and surface complexation, cation exchange, and mineral precipitation and dissolution. Reasonable matches between measured data and model results suggest that: (1) CO 2 dissolution in the groundwater causes calcite to dissolve. (2) Observed increases in the concentration of dissolved trace metals result likely from Ca +2 -driven ion exchange with clays (smectites) and sorption/desorption reactions likely involving Fe (hydr)oxides. (3) Bicarbonate from CO 2 dissolution appears to compete for sorption with anionic species such as HAsO 4 −2 , potentially increasing dissolved As levels in groundwater.

Conference Paper↗
USGS2010

Geochemical and mineralogical evidence for Sahara and Sahel dust additions to Quaternary soils on Lanzarote, eastern Canary Islands, Spain

Africa is the most important source of dust in the world today, and dust storms are frequent on the nearby Canary Islands. Previous workers have inferred that the Sahara is the most important source of dust to Canary Islands soils, with little contribution from the Sahel region. Soils overlying a late Quaternary basalt flow on Lanzarote, Canary Islands, contain, in addition to volcanic minerals, quartz and mica, exotic to the island's bedrock. Kaolinite in the soils also likely has an exotic origin. Trace-element geochemistry shows that the soils are derived from varying proportions of locally derived basalt and African dust. Major-element geochemistry, clay mineralogy and interpretation of satellite imagery suggest that dust additions to the Canary Islands come not only from the Sahara Desert, but also from the Sahel region. ?? Published 2010. This article is a US Government work and is in the public domain in the USA.

Terra Nova↗
USGS1959

Core logs from Searles Lake, San Bernardino County, California

Forty-one drill holes in the saline deposit on Searles Lake, San Bernardino County, Calif., were cored and logged. Drill holes averaged about 100 feet in depth; the majority are located around the margins of the dry lake. The saline deposit consists of an upper salt body about 39 square miles in area, of which 12 square miles are exposed in the central part of the lake, and a lower salt body of approximately the same areal extent found at greater depth. The 2 salt bodies are separated by a seam of clay or marl averaging about 12 feet thick. Isopach maps show the salt bodies are slightly elongated to the north; maximum thicknesses of the upper and lower salt bodies are 95 and 54 feet, respectively. Core logs, in written and graphic form, show the chief minerals of the saline bodies are halite, trona, hanksite, borax, and burkeite; relatively minor quantities of 13 additional minerals are described. The 41 drill-hole logs are shown graphically in columnar sections which give thicknesses, mineralogy, and mineral percentages; 15 representative written logs are published in full.

Bulletin↗
USGS2015

REE enrichment in granite-derived regolith deposits of the southeast United States: Prospective source rocks and accumulation processes

The Southeastern United States contains numerous anorogenic, or A-type, granites, which constitute promising source rocks for REE-enriched ion adsorption clay deposits due to their inherently high concentrations of REE. These granites have undergone a long history of chemical weathering, resulting in thick granite-derived regoliths, akin to those of South China, which supply virtually all heavy REE and Y, and a significant portion of light REE to global markets. Detailed comparisons of granite regolith profiles formed on the Stewartsville and Striped Rock plutons, and the Robertson River batholith (Virginia) indicate that REE are mobile and can attain grades comparable to those of deposits currently mined in China. A REE-enriched parent, either A-type or I-type (highly fractionated igneous type) granite, is thought to be critical for generating the high concentrations of REE in regolith profiles. One prominent feature we recognize in many granites and mineralized regoliths is the tetrad behaviour displayed in REE chondrite-normalized patterns. Tetrad patterns in granite and regolith result from processes that promote the redistribution, enrichment, and fractionation of REE, such as late- to post- magmatic alteration of granite and silicate hydrolysis in the regolith. Thus, REE patterns showing tetrad effects may be a key for discriminating highly prospective source rocks and regoliths with potential for REE ion adsorption clay deposits.

Conference Paper↗