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At least 595 records · Page 33Linked to original sources

USGS2017

Wisconsin Glaciation of the Sierra Nevada (79,000-15,000 yr B.P.) as recorded by rock flour in sediments of Owens Lake, California

Chemical analyses of the clay-sized fractions of 564 continuous sediment samples (200-yr resolution) from composite core OL90/92 allow quantification of an abundance of glacial rock flour. Rock flour produced during glacier advances is represented by clay-sized plagioclase, K-feldspar, and biotite in homogeneous internal composition. The abundance of rock flour is deemed proportional to the intensity of glacies advances. Age control for the composite section is provided by combining previously published radiocarbon dates on organics, U/Th dates on ostracode shells, and U/Th dates on saline minerals from nearby Searles Lake correlated to OL92 by pollen. The rock flour record displays three levels of variability: (1) a dominant one of about 20,000 yr related to summer insolation and precipitation; (2) an intermediate one of 3000-5000 yr, perhaps related to North Atlantic Heinrich events; and (3) a minor one of 1000-2000 yr, perhaps related to North Atlantic thermohaline-driven air-temperature variation. ?? 2001 University of Washington.

Quaternary Research↗

USGS1964

Origin of precambrian iron formations

A statistical study of the chemical composition of the Precambrian iron formations of the Canadian Shield affords a new approach to the origin of these unusual formations . The average total iron content of 2,200 samples from the literature and from unpublished mining company analyses is 26.7 percent Fe. The average Fe content for 16 iron formations in the United States and Canada ranges from 24.5 to 34.1 percent. Low contents of A1203, Ti02, P2O5, and CaO characterize the Precambrian iron formations compared to the relatively large amounts of these constituents in the post- Precambrian iron -bearing sediments. The chemical data emphasize that whereas iron , manganese, and silica were transported and deposited together in the cherty iron formations of the Precambrian , these same elements were chemically differentiated in younger geological time in large but separate deposits of iron and silica. Isotopic age determinations indicate that cherty iron formations were deposited during a long interval of geologic time from approximately 1,700 to 3,000 million years ago. A model is proposed to explain the origin of the iron formations of the Lake Superior type based on the absence or marked deficiency of free oxygen in the atmosphere prior to the Late Precambrian . Lateritic weathering under these conditions permitted the transport of iron and manganese together with silica. The weathered mantle effectively retained aluminum, titanium, phosphorus, and colloidal clay. Graphitic material of biogenic origin is closely associated with the Precambrian iron formations . Although it is uncertain whether iron was precipitated directly through biologic processes, the removal of C02 and the liberation of oxygen to the sea water through photosynthesis of primitive plants undoubtedly influenced the energy relationships among the iron minerals. As a result of the variable conditions the iron formations commonly are characterized by nonequilibrium mineral assemblages. In Late Precambrian time a critical level of free oxygen in the atmosphere was attained permitting a marked acceleration in plant growth and in accretion of oxygen. This stage in the development of an oxygenated atmosphere was reached at least 1,200 million years ago and effectively curtailed the development of cherty iron formations of the Lake Superior type.

Economic Geology↗

USGS1983

Preliminary appraisal of the hydrology of the Stigler area, Haskell County, Oklahoma

Bed rock in the Stigler area of southeastern Oklahoma consists principally of shale, siltstone, and sandstone of the McAlester, Savanna, and Boggy Formations of Pennsylvanian age. These rocks have been folded to form the Stigler syncline on the north and the Antioch anticline on the south. An area of several square miles is underlain by terrace deposits, mostly sandy silt, as much as 25 feet thick. Alluvium along the streams is 5 to 10 feet thick and consists mainly of sandy silt. Neither the terrace deposits nor the alluvium are hydrologically significant. Water in the bedrock is under artesian conditions. Well depths range from 34 to 235 feet and average 95 feet. The water level in most wells is less than 30 feet below the land surface. Because the rocks have minimal permeability, well yields probably are less than 5 gallons per minute. Much of the area is provided with water by a rural water district. Based on specific-conductance measurements, dissolved-solids concentrations in ground water are estimated to range from 200 to 2,500 milligrams per liter. Nor relationship between variations in specific conductance and well depth, geographic distribution, or geologic formation is apparent. Streams in the area are ephemeral and extended periods of no flow can be expected. During much of the period of record, streamflow in Taloka Creek was maintained by water pumped from an active coal mine. Water upstream from the mine area had a mean dissolved-solids concentration of 72 milligrams per liter whereas water downstream from the mine area had a mean concentration of 1,323 milligrams per liter. At times, downstream concentrations of some toxic metals exceeded the standards for drinking water set by the U.S. Environmental Protection Agency. Samples of water collected from Taloka Creek since mining ceased did not have excessive concentrations of toxic metals. Maximum suspended-sediment discharge of Taloka Creek was about 1,660 tons per day. Silt-clay particles (diameters less than 0.062 millimeter) were the dominant grain size. Observed and measured effects of surface mining for coal on the hydrologic system include (1) creation of additional water storage in the surface mine pond, (2) disruption of drainage in an area of about 1 square mile, and (3) increased mineralization of water in Taloka Creek. Other possible effects include (4) changes in permeability and storage of water in mine spoil, (5) minor changes in streamflow and runoff characteristics, and (6) temporary increase in the sediment load of Taloka Creek.

Water-Resources Investigations Report↗

USGS1973

Gold-bearing arsenian pyrite determined by microprobe analysis, Cortez and Carlin Gold Mines, Nevada

Studies of polished sections and chemical analyses made by electron microprobe show that gold and arsenic in the unoxidized ores from the Cortez and Carlin mines are most abundant in pyrite. Gold, as particles too small to be seen under the microscope, along with arsenic is concentrated in tiny pyrite grains (<0.005 mm) and in thin rims of larger pyrite grains. It is concentrated also in arsenopyrite which is sparsely distributed in the Cortez ore. Traces of gold are contained in sphalerite and chalcopyrite sparsely disseminated in Carlin ore. Mercury and antimony occur also in the pyrite, and antimony is in illite as well. Little if any gold or arsenic is contained in quartz, carbonate, clay, and carbonaceous material. In oxidized ore, the sulfur and carbonaceous material have been removed and gold and arsenic occur in iron oxide pseudomorphs after pyrite. Gold can be seen in the oxidized ore, indicating that it has been mobilized and concentrated. No association was found between gold and the carbonaceous material. During mineralization, calcite was removed from the fractured silty carbonate of the Roberts Mountains Formation, creating micropore space in which pyrite, quartz, and illite were deposited. The average tenor of the pyrite, if all the gold were in the pyrite, would be 0.10 percent at Cortez and 0.14 percent at Carlin. These calculated values are similar to the analytical values. The calculated tenor of the carbonaceous material, however-if such material were considered to be the mineral host of the gold-would be 0.28 percent at Cortez and 1 percent at Carlin. These figures are unreasonable when compared with the analytical data, which show that the carbonaceous material contains no detectable amounts of gold. © 1973 Society of Economic Geologists, Inc.

Nevada↗

USGS2013

Nickel-cobalt laterites: A deposit model

Nickel-cobalt (Ni-Co) laterite deposits are supergene enrichments of Ni±Co that form from intense chemical and mechanical weathering of ultramafic parent rocks. These regolith deposits typically form within 26 degrees of the equator, although there are a few exceptions. They form in active continental margins and stable cratonic settings. It takes as little as one million years for a laterite profile to develop. Three subtypes of Ni-Co laterite deposits are classified according to the dominant Ni-bearing mineralogy, which include hydrous magnesium (Mg)-silicate, smectite, and oxide. These minerals form in weathering horizons that begin with the unweathered protolith at the base, saprolite next, a smectite transition zone only in profiles where drainage is very poor, followed by limonite, and then capped with ferricrete at the top. The saprolite contains Ni-rich hydrous Mg-silicates, the Ni-rich clays occur in the transition horizon, and Ni-rich goethite occurs in the limonite. Although these subtypes of deposits are the more widely used terms for classification of Ni-Co laterite deposits, most deposits have economic concentrations of Ni in more than one horizon. Because of their complex mineralogy and heterogeneous concentrations, mining of these metallurgically complex deposits can be challenging. Deposits range in size from 2.5 to about 400 million tonnes, with Ni and Co grades of 0.66–2.4 percent (median 1.3) and 0.01–0.15 percent (median 0.08), respectively. Modern techniques of ore delineation and mineralogical identification are being developed to aid in streamlining the Ni-Co laterite mining process, and low-temperature and low-pressure ore processing techniques are being tested that will treat the entire weathered profile. There is evidence that the production of Ni and Co from laterites is more energy intensive than that of sulfide ores, reflecting the environmental impact of producing a Ni-Co laterite deposit. Tailings may include high levels of magnesium, sulfate, and manganese and have the potential to be physically unstable.

Scientific Investigations Report↗

USGS1979

Mineral resources of the Citico Creek Wilderness Study Area, Monroe County, Tennessee

The proposed Citico Creek Wilderness comprises about 5,670 hectares (56.7 km2) in the Cherokee National Forest south of the Little Tennessee River in easternmost Monroe County, Tennessee. Principal drainages are Citico Creek and Doublecamp Creek. Rocks of the study area include greenschist-facies arkosic metasandstone, metagraywacke, slate, and metaconglomerate of the Great Smoky Group of late Precambrian age. Minor deposits of unconsolidated Quaternary alluvium locally mantle the bedrock. Deformation is shown by asymmetric and overturned folds and by several major faults. More than 500 sample s of soil, rock, and stream sediment were collected and analyzed for 31 major, minor, and trace elements by semiquantitative spectrographic, atomic absorption, and fire assay methods No significant metal anomalies were detected. Concentrations of Cu, Co, As, Pb, and Zn slightly higher than background are found within sulfidic parts of a distinctive stratigraphic unit composed of graphitic slate and metagraywacke. Pyrite and pyrrhotite are the chief sulfide minerals, with traces o f accessory sphalerite, chalcopyrite, galena, and arsenopyrite occurring as microscopic intergrowths. A reconnaissance ground radiometric survey and subsequent neutron activation analyses of selected radioactive rock samples show that the sulfidic parts of the graphitic slate unit have a relatively high content of Th and U, but are not potentially economic. No metallic mineral resources appear to exist within the Citico Creek Wilderness Study Area. Resources of slate, silica, and stone are present, but they display no special qualities to differentiate them from other such material throughout the region. Ceramic evaluation tests on selected samples of slate indicate that the slate would have only marginal use for structural clay products such as brick and tile. Minor sand and gravel deposits occur along a few streams but are present in larger quantities and are more easily recovered in other areas.

Tennessee↗

USGS1971

Selected fluvial monazite deposits in the southeastern United States

Farther southwest in Georgia, around Griffin and Zebullon, along streams tributary to the Flint River in the monazite belt the flood plains are generally small and discontinuous, and only about 1 percent of the sediment is gravel. The area between Griffin, Zebullon, and the Flint River is underlain by biotite schist and biotite gneiss into which biotite granite has been intruded. Only along one stream, Flat Creek, which drains monazite-bearing granite near Zetella, Ga., are the tenors in monazite even moderately high, but a combination of thick, clayey overburden and discontinuous flood plains make the stream unsuitable for placer mining. Elsewhere in the Flint River area the heavy-mineral concentrates contain less than 1 percent monazite. The southwesternmost area in which reconnaissance of the monazite belt was conducted includes a groups of southwest-flowing tributaries to the Chattahoochee River north of Pine Mountain and near La Grange, Ga. A combination of three characteristics of the alluvium make the area unfavorable for mining: (1) the upper half of the sedimentary sequence is clay and silt, (2) there is scant gravel, and (3) much of the sand is fine grained. Monazite is associated with the Snelson Granite, schists, and gneisses north of the Towaliga fault, but even in this area the tenor of most riffle sediments is only 0.1 to 0.5 pound of monazite per cubic yard, and the average tenor of the alluvium is about 0.2 pound per cubic Yard. Rocks south of the Towaliga fault contain scant monazite. The monazite-bearing area in the drainage basin of the Chattahoochee River has no monazite placers. Evidence from the areas on the Flint and Chattahoochee Rivers shows that streams in western Georgia are a much poorer source of monazite than streams farther to the northeast in Georgia, South Carolina, and North Carolina. Also, the northeastern part of the belt in the drainage basins of the Yadkin and Dan Rivers is a poorer source for monazite than the area between the Savannah and Catawba Rivers, S.C.-N.C. Monazite-bearing crystalline rocks in the western belt contain about 0.06 pound of monazite per cubic yard. Residual soil derived from the crystalline rocks contains about 0.3 to 0.4 pound of monazite per cubic yard, and colluvial sediments formed by sheet-wash from saprolite, residual soil, and, rarely, old stream deposits, have an average of 3.1 pounds of monazite to the cubic yard. The data on the tenors of residual and colluvial deposits are far less comprehensive than those an the quantity of monazite in the crystalline rocks, but the tenors are probably of the correct order of magnitude. Neither the crystalline rocks nor the residual soils are ores of monazite. Because the colluvial deposits are thin and have patch distribution they could not be mined independently, but some colluvium could be stripped from the adjoining hills in conjunction with the mining of alluvial deposits in the valleys. It is most unlikely that alluvial monazite placers have formed in the trunk streams leading southeastward out of the monazite belt. Churn drilling on the Broad and North Tyger Rivers, South Carolina, at the east edge of the belt has shown that the bulk of the alluvium is fine-grained sediment that contains 0.2 to 0.4 pound of monazite per cubic yard--tenors that represent no considerable enrichment over those in the crystalline rocks and residual soils. The probable persistence of predominantly fine-grained alluvium downstream to the Coastal Plain and the certain dilution of monazite-bearing concentrates by the inflow of monazite-free suites of heavy minerals between the belt and the fall line suggest that the trunk streams east of the belt are the least favorable sources for alluvial monazite in the Piedmont?

Open-File Report↗

USGS2023

Stratigraphic architecture and fluvial interpretations of the Upper Cretaceous (Turonian?) Middendorf Formation, Chesterfield County, South Carolina, U.S.A.

The Upper Cretaceous (Turonian?) Middendorf Formation is a sand-rich stratigraphic unit of fluvial origin that forms a large aquifer in the U.S. Atlantic Coastal Plain. In Chesterfield County (South Carolina), which is the site of the type locality, the formation ranges in thickness from 66.5 to > 119.7 meters. The base of the formation is an unconformity above Paleozoic metasiltstone, and the upper contact is an unconformity above which lies sand of the Quaternary Pinehurst Formation. Outcrops display the following five facies assemblages: 1) sandstone to conglomeratic sandstone (fluvial bar and channel deposits), 2) beds of alternating laminae of sandstone and mudstone (fluvial overbank or floodplain deposits), 3) ≥ 1 m-thick beds of clay (swamp deposits, floodplain deposits, and/or sediment that accumulated in abandoned fluvial channels), 4) 0.2–0.5 m-thick planar to slightly undulatory beds of framework-supported sandstone with a mud matrix (traction-dominated current deposits at the top of fluvial bars, upper-flow-regime bedform deposits in subsidiary fluvial channels, or coarse-grained overbank deposits), and 5) sandstone to conglomeratic sandstone cemented by iron (interpreted as fluvial bar and channel deposits, with the iron cement being a diagenetic “groundwater ferricrete” that formed via the circulation of shallow groundwater and the oxidation of iron-bearing minerals). Kaolinite in various forms is pervasive throughout the formation and is interpreted as an early diagenetic phenomenon that formed by prolonged postdepositional weathering and flushing by meteoric water under a warm and humid paleoclimate. The fluvial system that formed the Middendorf Formation prograded into the area from the west or northwest from uplifted margins of Mesozoic rift basins and/or the Appalachian Mountains. This progradation was a response to a base-level fall and the sediment accumulated during base-level lowstand and subsequent early transgression. In Chesterfield County, the Middendorf Formation can be subdivided into three fining-upward sequences. Each sequence consists predominantly of medium to coarse sand with a greater abundance of gravel in the lower part of the sequence and a greater abundance of clay and silt beds in the upper part. Each sequence is interpreted as either a response to autogenic processes or a response to allogenic sea-level changes, specifically a higher-order (higher-frequency) progression from relative lowstand conditions to early transgression whereby coarse sand and gravel (e.g., fluvial bar and channel deposits) were preserved during initial lowstand conditions and a greater proportion of mud and finer-grained sand (floodplain deposits) were preserved during subsequent early transgression. The Middendorf Formation is correlative with several other kaolinite-rich fluvial sandstones in North America including the Raritan Formation in New Jersey, the Tuscaloosa Formation of the eastern Gulf of Mexico (Alabama, Mississippi, Louisiana), the Woodbine Formation of the central Gulf of Mexico (Texas), and the Frontier Formation of Wyoming. The accumulation and preservation of these formations occurred in response to a Turonian eustatic sea-level fall and subsequent transgression, and the early diagenetic kaolinite in these formations is attributed to similar warm and humid paleoclimate conditions.

South Carolina↗

USGS1979

Geology and industrial mineral resources of the Macon-Gordon kaolin district, Georgia

The Macon-Gordon kaolin district is about 80 miles (130 km) southeast of Atlanta, Georgia. It extends across the boundary between, and includes parts of, the Piedmont and Atlantic Coastal Plain physiographic provinces. The rocks in the Piedmont are mainly intensely folded sericite schist and granite gneiss containing irregular masses of amphibolite and feldspathic biotite gneiss and scattered igneous intrusive rocks. Most of the crystalline rocks are thought to be of Paleozoic age, but some of the intrusive rocks may be younger. The crystalline rocks are cut by a major unconformity and are overlain by sedimentary formations ranging in age from Cretaceous to Miocene. The valuable kaolin deposits occur in the Cretaceous beds, undivided, and in the Huber Formation which is of Paleocene to middle Eocene age. The resources of kaolin in the district are estimated in millions of metric tons as follows: reserves, 100; subeconomic resources, 700 to 900; undiscovered resources, probably 700 to 1,000. In addition to kaolin, the leading mineral commodity mined in the district, crushed stone and sand are now being produced, and fuller's earth and a minor amount of limestone were formerly produced. The crushed stone is quarried from igneous rocks in the Piedmont province. The sand is washed from the Cretaceous beds, undivided. The fuller's earth was mined from the Twiggs Clay Member of the Barnwell Formation, and limestone was dug from the Tivola Limestone.

Georgia↗

USGS2004

Summary of the hydrogeology of the Valley and Ridge, Blue Ridge, and Piedmont Physiographic Provinces in the eastern United States

The Appalachian Valley and Piedmont Regional Aquifer-System Analysis study (1988-1993) analyzed rock types in the 142,000-square-mile study area, identified hydrogeologic terranes, determined transmissivity distributions, determined the contribution of ground water to streamflow, modeled ground-water flow, described water quality, and identified areas suitable for the potential development of municipal and industrial ground-water supplies. Ground-water use in the Valley and Ridge, the Blue Ridge, and the Piedmont Physiographic Provinces exceeds 1.7 billion gallons per day. Thirty-three rock types in the study area were analyzed, and the rock types with similar water-yielding characteristics were combined and mapped as 10 hydrogeologic terranes. Based on well records, the interquartile ranges of estimated transmissivities are between 180 to 17,000 feet squared per day (ft 2 /d) for five hydrologic terranes in the Valley and Ridge; between 9 to 350 ft 2 /d for two terranes in the Blue Ridge; and between 9 to 1,400 ft 2 /d for three terranes in the Piedmont Physiographic Province. Based on streamflow records, the interquartile ranges of estimated transmissivities for all three physiographic provinces are between 290 and 2,900 ft 2 /d. The mean ground-water contribution to streams from 157 drainage basins ranges from 32 to 94 percent of mean streamflow with a median of 67 percent. In three small areas in two of the physiographic provinces, more than 54 percent of ground-water flow was modeled as shallow and local. Although ground-water chemical composition in the three physiographic provinces is distinctly different, the water generally is not highly mineralized, with a median dissolved-solids concentration of 164 milligrams per liter, and is mostly calcium, magnesium, and bicarbonate. Based on aquifer properties and current pumpage, areas favorable for the development of municipal and industrial ground-water supplies are underlain by alluvium of glacial origin near the northeastern part of the study area, by clay-free carbonate rocks primarily in the Valley and Ridge Physiographic Province, and by siliciclastic rocks in the three northernmost Mesozoic basins.

Alabama, Delaware, Georgia, Maryland, New Jersey, ↗

USGS1974

Geology and mineralogy of phosphate rock in the Bambui group near Cedro do Abaete and vicinity, Minas Gerais, Brazil

Discontinuous lenticular masses of phosphate rock are present near or at the contact between the green mudstone and the underlying red and yellow clay-stone units of the Serra da Saudade Member of the Rio Paraopeba Formation of the Bambui Group of late Precambrian to early Paleozoic age. The lenses are as much as 8 meters thick and 400 meters long. The phosphate rock is folded and faulted and is overlain by flat-lying rocks of Cretaceous age. The phosphate mineral is a carbonate fluorapatite, but only a small amount of C0 2 substitutes for PO 4 . Crystalline apatite in veinlets is clearly younger than the groundmass apatite, and contains almost no C0 2 . Surficial parts of the phosphate lenses have been altered to a rock characterized by aluminum phosphate. Samples of the green mudstone contain muscovite-illite, quartz, and what is believed to be glauconite. Samples collected adjacent to the phosphate lenses also contain veinlets of apatite or wavellite. Chemical analyses of the phosphate rock show that it contains from 16 to 35 percent P 2 0 5 , and all samples are deficient in Ca0 relative to P 2 0 5 , indicating that some of the phosphate in all samples is combined with alumina. The samples contain as much as 8 percent K 2 0 in the minerals muscovite-illite or glauconite. All the samples collected are extremely fine grained. The rocks are laminated and show the effects of slight deformation; for example, crumpled bedding, offset veinlets, and slight development of muscovite along bedding planes. The phosphate probably is not economically important on the world market, but possibly could be used locally for direct application depending on agricultural lands.

Minas Gerais↗

USGS2006

A 16-year record of eolian dust in Southern Nevada and California, USA: Controls on dust generation and accumulation

An ongoing project monitors modern dust accumulation in the arid southwestern United States to (1) determine the rate and composition of dust inputs to soils and (2) relate dust accumulation to weather patterns to help predict the effects of climate change on dust production and accumulation. The 16-year records of 35 dust-trap sites in the eastern Mojave Desert and southern Great Basin reveal how generation and accumulation of dust, including the silt-clay, carbonate, and soluble-salt fractions, is affected by the amount and seasonal distribution of rainfall and the behavior of different source types (alluvium, dry playas, and wet playas). Accumulation rates (fluxes) of the silt-clay fraction of dust, including carbonates, range from about 2-20 g/m2/yr. Average rates are higher in the southern part of the study area (south of latitude 36.5??N) and annually fluctuate over a larger range than rates in the northern part of the area. Sites throughout the study area show peaks in dust flux in the 1984-1985 sampling period and again in 1997-1999; northern sites also show increased flux in 1987-1988 and southern sites in 1989-1991. These peaks of dust flux correspond with both La Nina (dry) conditions and with strong El Nino (wet) periods. The accumulation rates of different components of mineral dusts fluctuate differently. For example, soluble-salt flux increases in 1987-1988, coincident with a moderate El Nino event, and increases very strongly in 1997-1999, overlapping with a strong El Nino event. Both of these high-rainfall winters were preceded and accompanied by strong summer rains. In contrast, little or no change in soluble-salt flux occurred during other periods of high winter rainfall but little summer rain, e.g. 1992-1995. The differences between northern vs. southern sites and between sites with playa dust sources vs. alluvial dust sources indicate that regional differences in the response of precipitation and vegetation growth to ENSO influence and differences in the response of source types control dust production and accumulation. A major factor is the hydrologic condition of surface sediments. The silt-clay and soluble-salt fluxes increased during the El Nino events of 1987-1988 and 1997-1998 at sites close to "wet" playas with shallow depths to groundwater (<10 m), consistent with the concept that active evaporative concentration of salts disrupts surface crusts and increases the susceptibility of surface sediment to deflation. The silt-clay flux also increased during drought periods (1989-1991, 1995-1997) at sites downwind of alluvial sources and "dry" playas with deeper groundwater (<10 m). These increases are probably related to the die-off of drought-stressed vegetation on alluvial sediments, and in some cases to local runoff events that deliver fresh sediment to playa margins and distal portions of alluvial fans. ?? 2006 Elsevier Ltd. All rights reserved.

Journal of Arid Environments↗

USGS2008

Hydrated silicate minerals on Mars observed by the Mars Reconnaissance Orbiter CRISM instrument

Phyllosilicates, a class of hydrous mineral first definitively identified on Mars by the OMEGA (Observatoire pour la Mineralogie, L’Eau, les Glaces et l’Activitié) instrument 1 , 2 , preserve a record of the interaction of water with rocks on Mars. Global mapping showed that phyllosilicates are widespread but are apparently restricted to ancient terrains and a relatively narrow range of mineralogy (Fe/Mg and Al smectite clays). This was interpreted to indicate that phyllosilicate formation occurred during the Noachian (the earliest geological era of Mars), and that the conditions necessary for phyllosilicate formation (moderate to high pH and high water activity 3 ) were specific to surface environments during the earliest era of Mars’s history 4 . Here we report results from the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) 4 of phyllosilicate-rich regions. We expand the diversity of phyllosilicate mineralogy with the identification of kaolinite, chlorite and illite or muscovite, and a new class of hydrated silicate (hydrated silica). We observe diverse Fe/Mg-OH phyllosilicates and find that smectites such as nontronite and saponite are the most common, but chlorites are also present in some locations. Stratigraphic relationships in the Nili Fossae region show olivine-rich materials overlying phyllosilicate-bearing units, indicating the cessation of aqueous alteration before emplacement of the olivine-bearing unit. Hundreds of detections of Fe/Mg phyllosilicate in rims, ejecta and central peaks of craters in the southern highland Noachian cratered terrain indicate excavation of altered crust from depth. We also find phyllosilicate in sedimentary deposits clearly laid by water. These results point to a rich diversity of Noachian environments conducive to habitability.

Nature↗

USGS2022

Development and description of a composite hydrogeologic framework for inclusion in a geoenvironmental assessment of undiscovered uranium resources in Pliocene- to Pleistocene-age geologic units of the Texas Coastal Plain

A previously completed mineral resources assessment of the Texas Coastal Plain indicated the potential for the future discovery of uranium resources. Geoenvironmental assessments that include the hydrogeologic framework can be used as a tool to understand the potential effects of mining operations. The hydrogeologic framework for this study focused on the composite hydrogeologic unit of the tract permissive for the occurrence of uranium consisting of the upper part of the Miocene-age Fleming Formation/Lagarto Clay, Pliocene-age Goliad and Pleistocene-age Willis Sands, Pleistocene-age Lissie and Beaumont Formations, and Holocene-age alluvial sediments (fluvial alluvium and eolian sand deposits). This composite hydrogeologic unit, which contains the Chicot and Evangeline aquifers of the Gulf Coast aquifer system, is intended for inclusion in a regional-scale geoenvironmental assessment of as yet undiscovered uranium resources. This article provides (1) a brief literature review describing the geologic and hydrogeologic settings, (2) the methodology used to develop a composite hydrogeologic framework, and (3) descriptions and maps of the land-surface altitude, composite hydrogeologic unit base and midpoint depth, water-level altitude, depth of water, unsaturated and saturated zone thickness, and transmissivity and hydraulic conductivity. A composite hydrogeologic unit, created by combining geologic and hydrogeologic data and maps for individual geologic and hydrogeologic units, is intended for use as a tool in a geoenvironmental assessment to evaluate potential contaminant migration through various avenues. Potential applications include using the hydrogeologic framework as an input into a geoenvironmental assessment to help estimate the potential for (1) runoff of contaminants into surface water, (2) infiltration of contaminants into the groundwater (aquifers), or (3) movement of contaminants from the mining area through wind, groundwater-flow, or streamflow in a given permissive tract. The procedures outlined in this paper also provide a method for developing hydrogeologic frameworks that can be applied in other areas where mining may occur.

Texas↗

USGS1984

Geologic and hydrologic characterization and evaluation of the Basin and Range Province relative to the disposal of high-level radioactive waste: Part I, Introduction and guidelines

The U.S. Geological Survey's program for geologic and hydrologic evaluation of physiographic provinces to identify areas potentially suitable for locating repository sites for disposal of high-level nuclear wastes was announced to the Governors of the eight States in the Basin and Range Province on May 5, 1981. Representatives of Arizona, California, Idaho, New Mexico, Nevada, Oregon, Texas, and Utah, were invited to cooperate with the Federal Government in the evaluation process. Each Governor was requested to nominate an Earth scientist to represent the State in a province working group composed of State and U.S. Geological Survey representatives. This report, Part I of a three-part report, provides the background, introduction and scope of the study. This part also includes a discussion of geologic and hydrologic guidelines that will be used in the evaluation process and illustrates geohydrologic environments and the effect of individual factors in providing multiple natural barriers to radionuclide migration. Part II is a reconnaissance characterization of the geologic and hydrologic factors to be used in the initial screening of the Basin and Range Province. Part III will be the initial evaluation of the Province and will identify regions that appear suitable for further study. The plan for study of the Province includes a stepwise screening process by which successively smaller land units are considered in increasing detail. Each step involves characterization of the geology and hydrology and selection of subunits for more intensive characterization. Selection of subunits for further study is by evaluation of geologic and hydrologic conditions following a set of guidelines. By representation on the Province Working Group, the States participate in a consultation and review role in: (1) Establishing geologic and hydrologic guidelines, and (2) characterizing and evaluating the Province. The States also participate in compilation of geologic and hydrologic data used in characterizing the Province. The current (1983) needs for a high-level radioactive waste repository include: (1) Disposal in a mined repository; (2) retrievability of the waste for as much as 50 years; and (3) confidence of isolation of the waste from the accessible environment. Isolation of the waste needs to be assured using geologic and hydrologic conditions that: (1) Minimize risk of inadvertent future intrusions by man; (2) minimize the possibility of disturbance by processes that would expose the waste or increase its mobility; and (3) provide a system of natural barriers to the migration of waste by ground water. The guidelines adopted by the Province Working Group are designed to provide a standard with which these conditions can be compared. The guidelines can be grouped into four principal categories: (1) Potential host media, (2) ground-water conditions, (3) tectonic conditions, and. (4) occurrence of natural resources. Ideally the host medium constitutes the first natural barrier to migration of radionculides. The host medium ideally should be a rock type that prevents or retards dissolution and transport of radionuclides. Rocks in both the saturated and unsaturated zones may have desirable characteristics for host media. Rocks-other than the host-in the ground-water flow path from the repository ideally should be major barriers to radionuclide migration. Confining beds of low permeability might be present to retard the rate of flow between more permeable beds. Additionally, sorption of radionuclides by materials such as clays and zeolites in the flow path can further retard the flow of radionuclides by several orders of magnitude. Tectonic conditions in an area should not present a probable cause for exhumation or increased mobility of radioactive waste. Natural resources are a factor for consideration because of the problem of future human intrusion and exposure to radioactivity in the quest for minerals, oil, gas, water, and geothermal resources. The ultimate evaluation of the suitability of a geohydrologic environment for developing a mined repository needs to assess all geologic and hydrologic characteristics and their interaction in providing confidence that a geohydrologic environment will effectively isolate radionuclides from human access. Several hypothetical settings with typical geohydrologic conditions in the Basin and Range Province are used to illustrate the effect of multiple barriers in the isolation of radionuclides.

Arizona, California, Idaho, Nevada, New Mexico, Or↗

USGS2009

The Eocene-Oligocene sedimentary record in the Chesapeake Bay impact structure: Implications for climate and sea-level changes on the western Atlantic margin

A multidisciplinary investigation of the Eocene-Oligocene transition in the International Continental Scientific Drilling Program (ICDP)-U.S. Geological Survey (USGS) Eyreville core from the Chesapeake Bay impact basin was conducted in order to document environmental changes and sequence stratigraphic setting. Planktonic foraminifera and calcareous nannofossil biostratigraphy indicate that the Eyreville core includes an expanded upper Eocene (Biozones E15 to E16 and NP19/20 to NP21, respectively) and a condensed Oligocene-Miocene (NP24-NN1) sedimentary sequence. The Eocene-Oligocene contact corresponds to a =3-Ma-long hiatus. Eocene- Oligocene sedimentation is dominated by great diversity and varying amounts of detrital and authigenic minerals. Four sedimentary intervals are identified by lithology and mineral content: (1) A 30-m-thick, smectite- and illite-rich interval directly overlies the Exmore Formation, suggesting long-term reworking of impact debris within the Chesapeake Bay impact structure. (2) Subsequently, an increase in kaolinite content suggests erosion from soils developed during late Eocene warm and humid climate in agreement with data derived from other Atlantic sites. However, the kaolinite increase may also be explained by change to a predominant sediment input from outside the Chesapeake Bay impact structure caused by progradation of more proximal facies belts during the highstand systems tract of the late Eocene sequence E10.Spectral analysis based on gamma-ray and magnetic susceptibility logs suggests infl uence of 1.2 Ma low-amplitude oscillation of the obliquity period during the late Eocene. (3) During the latest Eocene (Biozones NP21 and E16), several lithological contacts (clay to clayey silt) occur concomitant with a prominent change in the mineralogical composition with illite as a major component: This lithological change starts close to the Biozone NP19/20-NP21 boundary and may correspond to sequence boundary E10-E11 as observed in other northwest Atlantic margin sections. It could result from a shift to more distal depositional environments and condensed sedimentation during maximum fl ooding, rather than refl ecting a climatic change in the hinterland. The distinct 1% increase of the oxygen isotopes may correspond to the short-term latest Eocene "precursor isotope event." (4) The abrupt increase of sediment grainsize, carbonate content, and abundance of authigenic minerals (glauconite) across the major unconformity that separates Eocene from Oligocene sediments in the Eyreville core refl ects deposition in shallower settings associated with erosion, winnowing, and reworking. Sediments within the central crater were affected by the rapid eustatic sea-level changes associated with the greenhouse-icehouse transition, as well as by an abrupt major uplift event and possibly enhanced current activity on the northwestern Atlantic margin. ?? 2009 The Geological Society of America.

Chesapeake Bay↗

USGS1996

MUDMASTER: A Program for Calculating Crystalline Size Distributions and Strain from the Shapes of X-Ray Diffraction Peaks

Particle size may strongly influence the physical and chemical properties of a substance (e.g. its rheology, surface area, cation exchange capacity, solubility, etc.), and its measurement in rocks may yield geological information about ancient environments (sediment provenance, degree of metamorphism, degree of weathering, current directions, distance to shore, etc.). Therefore mineralogists, geologists, chemists, soil scientists, and others who deal with clay-size material would like to have a convenient method for measuring particle size distributions. Nano-size crystals generally are too fine to be measured by light microscopy. Laser scattering methods give only average particle sizes; therefore particle size can not be measured in a particular crystallographic direction. Also, the particles measured by laser techniques may be composed of several different minerals, and may be agglomerations of individual crystals. Measurement by electron and atomic force microscopy is tedious, expensive, and time consuming. It is difficult to measure more than a few hundred particles per sample by these methods. This many measurements, often taking several days of intensive effort, may yield an accurate mean size for a sample, but may be too few to determine an accurate distribution of sizes. Measurement of size distributions by X-ray diffraction (XRD) solves these shortcomings. An X-ray scan of a sample occurs automatically, taking a few minutes to a few hours. The resulting XRD peaks average diffraction effects from billions of individual nano-size crystals. The size that is measured by XRD may be related to the size of the individual crystals of the mineral in the sample, rather than to the size of particles formed from the agglomeration of these crystals. Therefore one can determine the size of a particular mineral in a mixture of minerals, and the sizes in a particular crystallographic direction of that mineral.

Open-File Report↗

USGS2017

Rare-earth elements

The rare-earth elements (REEs) are 15 elements that range in atomic number from 57 (lanthanum) to 71 (lutetium); they are commonly referred to as the “lanthanides.” Yttrium (atomic number 39) is also commonly regarded as an REE because it shares chemical and physical similarities and has affinities with the lanthanides. Although REEs are not rare in terms of average crustal abundance, the concentrated deposits of REEs are limited in number. Because of their unusual physical and chemical properties, the REEs have diverse defense, energy, industrial, and military technology applications. The glass industry is the leading consumer of REE raw materials, which are used for glass polishing and as additives that provide color and special optical properties to the glass. Lanthanum-based catalysts are used in petroleum refining, and cerium-based catalysts are used in automotive catalytic converters. The use of REEs in magnets is a rapidly increasing application. Neodymium-iron-boron magnets, which are the strongest known type of magnets, are used when space and weight are restrictions. Nickel-metal hydride batteries use anodes made of a lanthanum-based alloys. China, which has led the world production of REEs for decades, accounted for more than 90 percent of global production and supply, on average, during the past decade. Citing a need to retain its limited REE resources to meet domestic requirements as well as concerns about the environmental effects of mining, China began placing restrictions on the supply of REEs in 2010 through the imposition of quotas, licenses, and taxes. As a result, the global rare-earth industry has increased its stockpiling of REEs; explored for deposits outside of China; and promoted new efforts to conserve, recycle, and substitute for REEs. New mine production began at Mount Weld in Western Australia, and numerous other exploration and development projects noted in this chapter are ongoing throughout the world. The REE-bearing minerals are diverse and often complex in composition. At least 245 individual REE-bearing minerals are recognized; they are mainly carbonates, fluorocarbonates, and hydroxylcarbonates (n = 42); oxides (n = 59); silicates (n = 85); and phosphates (n = 26). Many of the world’s significant REE deposits occur in carbonatites, which are carbonate igneous rocks. The REEs also have a strong genetic association with alkaline magmatism. The systematic geologic and chemical processes that explain these observations are not well understood. Economic or potentially economic REE deposits have been found in (a) carbonatites, (b) peralkaline igneous systems, (c) magmatic magnetite-hematite bodies, (d) iron oxide-copper-gold (IOCG) deposits, (e) xenotime-monazite accumulations in mafic gneiss, (f) ion-absorption clay deposits, and (g) monazite-xenotime-bearing placer deposits. Carbonatites have been the world’s main source for the light REEs since the 1960s. Ion-adsorption clay deposits in southern China are the world’s primary source of the heavy REEs. Monazite-bearing placer deposits were important sources of REEs before the mid-1960s and may be again in the future. In recent years, REEs have been produced from large carbonatite bodies mined at the Mountain Pass deposit in California and, in China, at the Bayan Obo deposit in Nei Mongol Autonomous Region, the Maoniuping deposit in Sichuan Province, the Daluxiang deposit in Sichuan Province, and the Weishan deposit in Anhui Province. Alkaline igneous complexes have recently been targeted for exploration because of their enrichments in the heavy REEs. Information relevant to the environmental aspects of REE mining is limited. Little is known about the aquatic toxicity of REEs. The United States lacks drinking water standards for REEs. The concentrations of REEs in environmental media are influenced by their low abundances in crustal rocks and their limited solubility in most groundwaters and surface waters. The scarcity of sulfide minerals, including pyrite, minimizes or eliminates concerns about acid-mine drainage for carbonatite-hosted deposits and alkaline-intrusion-related REE deposits. For now, insights into environmental responses of REE mine wastes must rely on predictive models.

Professional Paper↗