USGS Science⌕ Search

Geology topics

Eugene E. Foord

Publications and source records attributed to Eugene E. Foord.

15 recordsLinked to original sources
USGS2024

Reassessment of the volkonskoite-chromian smectite nomenclature problem.

The name volkonskoite was first used in 1830 to describe a bright blue-green, chromium-bearing clay material from the Okhansk region, west of the Ural Mountains, U.S.S.R. Since that time, the name has been applied to numerous members of the smectite group of clay minerals, although the reported chromium content has ranged from 1% to about 30% Cr 2 O 3 . The name has also been applied to some chromian chlorites. Because volkonskoite has been used for materials that differ not only in their chromium content but also in their basic structure, the species status of the mineral has been unclear. To resolve this uncertainty, two specimens of volkonskoite from (1) Mount Efimiatsk, the type locality in the Soviet Union (USNM 16308) and (2) the Okhansk region in the Perm Basin, U.S.S.R. (USNM R4820), were examined by several mineralogical techniques. Neotype sample 16308 has the following structural formula: (Ca 0.11 Mg 0.11 Fe 2+ 0.03 K 0.02 )(Cr 1.18 Mg 0.78 Fe 3+ 0.29 Ca 0.02 )(Si 3.50 Al 0.51 )O 10 (OH) 2 ⋅3.64H 2 O. Sample R4820 has the following structural formula: (Ca 0.25 Mg 0.05 Fe 2+ 0.01 K 0.03 Mn 0.01 )(Cr 1.07 Mg 0.75 Fe 3+ 0.35 (Si 3.59 Al 0.43 )O 10 (OH) 2 ⋅4.22H 2 O. Mössbauer spectroscopy indicates that 91% and 98% of the iron is present as Fe 3+ in samples 16308 and R4820, respectively. X-ray powder diffraction patterns of both samples have broad lines corresponding to minerals of the smectite group. On the basis of these data, volkonskoite appears to be a dioctahedral member of the smectite group that contains chromium as the dominant cation in the octahedral layer. Smectites containing less than this amount of octahedral chromium should not be called volkonskoite, but should be named by chemical element adjectives, e.g., chromian montmorillonite, chromian nontronite.

Clays and Clay Minerals↗
USGS2024

Phosphates in some Missouri refractory clays

This paper describes in detail phosphate minerals occurring in refractory clays of Missouri and their effect on the refractory degree of the clays. The minerals identified include carbonate-fluorapatite (francolite), crandallite, goyazite, wavellite, variscite and strengite. It is emphasized that these phosphates occur only in local isolated concentrations, and not generally in Missouri refractory clays. The Missouri fireclay region comprises 2 districts, northern and southern, separated by the Missouri River. In this region, clay constitutes a major part of the Lower Pennsylvanian Cheltenham Formation. The original Cheltenham mud was an argillic residue derived from leaching and dissolution of pre-Pennsylvanian carbonates. The mud accumulated on a karstic erosion surface truncating the pre-Cheltenham rocks. Fireclays of the northern district consist mainly of poorly ordered kaolinite, with variable but minor amounts of illite, chlorite and fine-grained detrital quartz. Clays of the southern district were subjected to extreme leaching that produced well-ordered kaolinite flint clays. Local desilication formed pockets of diaspore, or more commonly, kaolinite, with oolite-like nubs or burls of diaspore (“burley”" clay). The phosphate-bearing materials have been studied by X-ray diffraction (XRD), scanning electron microscopy-energy dispersive spectral analysis (SEM-EDS) and chemical analysis. Calcian goyazite was identified in a sample of diaspore, and francolite in a sample of flint clay. A veinlet of wavellite occurs in flint clay at one locality, and a veinlet of variscite-strengite at another locality. The Missouri flint-clay-hosted francolite could not have formed in the same manner as marine francolite. The evidence suggests that the Cheltenham francolite precipitated from ion complexes in pore water, nearly simultaneously with crystallization of kaolinite flint clay from an alumina-silica gel. Calcian goyazite is an early diagenetic addition to its diaspore host. The wavellite and variscite-strengite veinlets are secondary, precipitated from ion complexes in ground water percolating along cracks in the flint clay. The flint clay host of the variscite-strengite veinlet contains strontian crandallite. All of the phosphates contain significant amounts of strontium. The source of P, Ca and Sr was the marine carbonates. Dissolution of these carbonates produced the argillic residue that became the primordial Cheltenham paludal mud, which ultimately altered to fireclay. Preliminary firing tests show that the presence of phosphates lowers fusion temperature. However, it is not clear whether poor refractoriness is due to the presence of phosphates, per se, or to Ca, Sr and other alkaline elements present in the phosphates.

Clays and Clay Minerals↗
USGS2018

Zinc- and Y-group-bearing senaite from St Peters Dome, and new data on senaite from Dattas, Minas Gerais, Brazil

A Zn- and Y-group-bearing senaite, formulated as AM 21 O 38 (Pb 0.63 Na 0.46 Ba 0.11 ) Σ1.20 (Ti 14.64 Zn 1.74 Y‒group REE 0.70 Mn 0.38 Nb 0.20 Sn 0.03 Zr 0.03 Th 0.02 ) Σ20.9 O 38 , a member of the crichtonite group, is a newly characterized phase associated with murataite at the St Peters Dome area, Colorado. The Zn- and Y-group-bearing senaite is uranium-free and nonmetamict, but otherwise is comparable to known senaites and davidites in X-ray diffraction pattern, symmetry, and structure. The REE distribution shows a strong dominance of Y and the Y-group REE which are present in M (1). Megascopically, the mineral is black, submetallic, and opaque; in polished section it appears to be white and moderately bright compared with murataite. Cleavage is absent but twinning on {52 0} is present. Senaite and hitherto unreported zinc-bearing senaite from Dattas, Diamantina, Minas Gerais, Brazil, have the following respective structural formulas as determined by electron microprobe: (Pb 0.76 Sr 0.20 La 0.08 Ce 0.07 Ba 0.04 ) Σ1.15 (Ti 12.89 Mn 0.88 Y 0.59 Zn 0.12 Mg 0.07 Nb 0.03 Cr 0.02 Th 0.02 ) Σ20.61 O 38 and (Pb 0.89 Ba 0.15 Ce 0.02 Sr 0.02 ) Σ1.08 (Ti 14.57 Zn 1.76 Na 0.63 Mn 0.50 Y 0.28 Nb 0.14 Mg 0.04 Cr 0.02 ) Σ20.83 O 38

Dattas, Minas Gerais↗
USGS2018

Uranoan thorite in lithophysal rhyolite - Topaz Mountain, Utah, U.S.A.

Uranoan thorite crystals have been found occurring as a sparse constituent in lithophysae in 6.1 to 6.8 Ma alkali rhyolite flows at Thomas Mountain, Utah, USA. The crystals are associated with sandidine, quartz, topaz, hematite, magnetite, and calcite; they are leek to dark grass green, transparent, well-formed, euhedral prisms, showing development of forms {100}, {101}, and {111}. The mineral is both optically isotropic, with a refractive index of 1.86(1), and X-ray amorphous, indicating its metamict state. Electron microprobe analysis yields: SiO 2 17.3, ThO 2 56.8, UO 2 25.4, total 99.5%, and a structural formula of (Th 0.72 U 0.31 ) Σ1.03 Si 0.97 O 4 . This appears to be the first reported occurrence of thorite in volcanic rocks of rhyolitic composition, and may account for part or all of the Th reported in alkali rhyolites and so-called ‘topaz-rhyolites’ of the western USA.

Utah↗
USGS2018

Meurigite, a new fibrous iron phosphate resembling kidwellite

Meurigite is a new hydrated potassium iron phosphate related to kidwellite and with structural similarities to other late-stage fibrous ferric phosphate species. It has been found at four localities so far — the Santa Rita mine, New Mexico, U.S.A.; the Hagendorf-Sud pegmatite in Bavaria, Germany; granite pegmatite veins at Wycheproof, Victoria, Australia; and at the Gold Quarry Mine, Nevada, U.S.A. The Santa Rita mine is the designated type locality. Meurigite occurs as tabular, elongated crystals forming spherical and hemispherical clusters and drusy coatings. The colour ranges from creamy white to pale yellow and yellowish brown. At the type locality, the hemispheres may reach 2 mm across, but the maximum diameter reached in the other occurrences is usually less than 0.5 mm. A wide variety of secondary phosphate minerals accompanies meurigite at each locality, with dufrenite, cyrilovite, beraunite, rockbridgeite and leucophosphite amongst the most common. Vanadates and uranates occur with meurigite at the Gold Quarry mine. Electron microprobe analysis and separate determination of H 2 O and CO 2 on meurigite from the type locality gave a composition for which several empirical formulae could be calculated. The preferred formula, obtained on the basis of 35 oxygen atoms, is which simplies Qualitative analyses only were obtained for meurigite from the other localities, due to the softness and openness of the aggregates. Because of the fibrous nature of meurigite, it was not possible to determine the crystal structure, hence the exact stoichiometry remains uncertain. The lustre of meurigite varies from vitreous to waxy for the Santa Rita mine mineral, to silky for the more open sprays and internal surfaces elsewhere. The streak is very pale yellow to cream and the estimated Mohs hardness is about 3. Cleavage is perfect on {001} and fragments from the type material have a mean specific gravity of 2.96. The strongest lines in the X-ray powder pattern for the type material are ( d obs , I obs , hkl ) 3.216(100)404; 4.84(90)111; 3.116(80)205; 4.32(70)112; 9.41(60)201; 3.470(60)800. The X-ray data were indexed on the basis of a monoclinic unit cell determined from electron diffraction patterns. The cell parameters, refined by least squares methods, are a = 29.52(4), b = 5.249(6), c = 18.26(1) Å, β = 109.27(7)°, V = 2672(3) Å 3 , and Z = 4. The calculated density is 2.89 gcm −3 . The space group is either C 2, Cm or C 2 / m . X-ray powder data for meurigite are closely similar to those for kidwellite and phosphofibrite, but meurigite appears to be characterised by a strong 14 Å reflection. The relationship between these three minerals remains uncertain in the absence of structural data. On the available evidence, meurigite and kidwellite are not the respective K and Na-endmembers of a solid solution series. The meurigite cell parameters suggest it belongs to a structural family of fibrous ferric phosphates, such as rockbridgeite, dufrenite and beraunite, which have a discrete 5 Å fibre axis. Meurigite occurs in widely varying environments, its formation probably favoured by late-stage solutions rich in K rather than Na.

Mineralogical Magazine↗
USGS2003

Geochemistry, geochronology, mineralogy, and geology suggest sources of and controls on mineral systems in the southern Toquima Range, Nye County, Nevada

Geochemistry maps showing the distribution and abundance of 18 elements in about 1,400 rock samples, both mineralized and unmineralized, from the southern Toquima Range, Nev., indicate major structural and lithologic controls on mineralization, and suggest sources of the elements. Radiometric age data, lead mineralogy and paragenesis data, and lead-isotope data supplement the geochemical and geologic data, providing further insight into timing, sources, and controls on mineralization. Major zones of mineralization are centered on structural margins of calderas and principal northwest-striking fault zones, as at Round Mountain, Manhattan, and Jefferson mining districts, and on intersections of low-angle and steep structures, as at Belmont mining district. Paleozoic sedimentary rocks, mostly limestones (at Manhattan, Jefferson, and Belmont districts), and porous Oligocene ash-flow tuffs (at Round Mountain district) host the major deposits, although all rock types have been mineralized as evidenced by numerous prospects throughout the area. Principal mineral systems are gold-silver at Round Mountain where about 7 million ounces of gold and more than 4 million ounces of silver has been produced; gold at Gold Hill in the west part of the Manhattan district where about a half million ounces of gold has been produced; gold-mercury-arsenic-antimony in the east (White Caps) part of the Manhattan district where a few hundred thousand ounces of gold has been produced; and silver-lead-antimony at Belmont where more than 150,000 ounces of silver has been produced. Lesser amounts of gold and silver have been produced from the Jefferson district and from scattered mines elsewhere in the southern Toquima Range. A small amount of tungsten was produced from mines in the granite of the Round Mountain pluton exposed east of Round Mountain, and small amounts of arsenic, antimony, and mercury have been produced elsewhere in the southern Toquima Range. All elements show unique distribution patterns that suggest specific sources and lithologic influences on deposition, as well as multiple episodes of mineralization. Principal episodes of mineralization are Late Cretaceous (molybdenum and tungsten in and near granite; silver at Belmont and Silver Point mines), early Oligocene [tourmaline and base- and precious-metals around the granodiorite of Dry Canyon stock as well as at Manhattan(?)], late Oligocene (gold at Round Mountain and Jefferson), and Miocene (gold at Manhattan). Most likely principal sources of molybdenum, tungsten, silver, and bismuth are Cretaceous granites; of antimony, arsenic, and mercury are intermediate-composition early Oligocene intrusives; and of gold are early and late Oligocene and early Miocene magmas of the volcanic cycle. Lead may have been derived principally from Cretaceous granitic magma and Paleozoic sedimentary rocks. Several areas prospective for undiscovered mineral deposits are suggested by spatial patterns of element distributions related to geologic features. The Manhattan district in the vicinity of the White Caps mine may be underlain by a copper-molybdenum porphyry system related to a buried stock; peripheral high-grade gold veins and skarn deposits may be present below deposits previously mined. The Jefferson district also may be underlain by a copper-molybdenum porphyry system related to a buried stock, it too with peripheral high-grade gold deposits. The Bald Mountain Canyon belt of small gold veins has potential for deeper deposits in buried porous ash-flow tuff similar to the huge Round Mountain low-grade gold-silver deposit. Several other areas have potential for a variety of mineral deposits. Altogether the geochemical, geochronologic, mineralogic, and geologic evidence suggests recurring mineralizing episodes of varied character, from Late Cretaceous to late Tertiary time, related to a long-lived hot spot deep in the crust or in the upper mantle. Granite plutons of Late Cretaceous age were minerali

Nevada↗
USGS1999

Cooling rates and crystallization dynamics of shallow level pegmatite-aplite dikes, San Diego County, California

Pegmatites of the Pala and Mesa Grande Pegmatite Districts, San Diego County, California are typically thin, sheet-like composite pegmatite-aplite dikes. Aplitic portions of many dikes display pronounced mineralogical layering referred to as "line rock," characterized by fine-grained, garnet-rich bands alternating with albite- and quartz-rich bands. Thermal modeling was performed for four dikes in San Diego County including the 1 m thick Himalaya dike, the 2 m thick Mission dike, the 8 m thick George Ashley dike, and the 25 m thick Stewart dike. Calculations were based on conductive cooling equations accounting for latent heat of crystallization, a melt emplacement temperature of 650 °C into 150 °C fractured, gabbroic country rock at a depth of 5 km, and an estimated 3 wt% initial H 2 O content in the melt. Cooling to <550 °C at the center of each dike occurred in ~9 years for the Stewart dike, ~340 days for the George Ashley dike, ~22 days for the Mission dike, and ~5 days for the Himalaya dike. Based on these calculations, growth rates for large pegmatitic minerals such as the 10 cm long Himalaya hanging wall tourmaline crystals may have been on the order of 10 -5 cm/s. Crystal size distribution (CSD) studies of garnet from layered aplites suggest growth rates of about 10 -6 cm/s. These results indicate that the dikes cooled and crystallized rapidly, with variable nucleation rates but high overall crystal-growth rates. Initial high nucleation rates coincident with emplacement and strong undercooling can account for the millimeter-size aplite grains. Lower nucleation rates coupled with high growth rates can explain the decimeter-size minerals in the hanging walls, cores, and miarolitic cavities of the pegmatites. The presence of tourmaline and/or lepidolite throughout these dikes suggests that although the melts were initially H 2 O-undersaturated, high melt concentrations of incompatible (or fluxing) components such as B, F, and Li (&plusmn;H 2 O), aided in the development of large pegmatitic crystals that grew rapidly in the short times suggested by the conductive cooling models.

American Mineralogist↗
USGS1996

Chronology of Late Cretaceous igneous and hydrothermal events at the Golden Sunlight gold-silver breccia pipe, southwestern Montana

Gold mineralization at the Golden Sunlight breccia pipe, southwestern Montana, is related to emplacement of Late Cretaceous alkali-calcic rhyolite and subsequent collapse of the Belt Supergroup wallrock and rhyolite in the pipe. The pipe is inferred to grade downward into an alkalic porphyry molybdenum system. The pipe is cut by alkalic to sub-alkalic lamprophyre dikes and sills, which locally contain high-grade gold where emplaced along late shear zones and vein systems. Determination of the emplacement age of the rhyolite is hampered by inherited lead or inherited Late Archean zircon from the source region of the rhyolite. An emplacement age of about 80 Ma for the rhyolite can be inferred if a basement age of 2,600 Ma is assumed. This Late Archean age is in agreement with basement ages determined in many parts of southwestern Montana. A 206 Pb- 238 U whole-rock date of 84 ? 18 Ma from altered and mineralized Belt Supergroup strata and rhyolite in the breccia pipe indicates hydrothermal alteration related to gold mineralization in Late Cretaceous time. Although sericite is a relatively widespread hydrothermal mineral, attempts to date the very fine grained material by the 40 Ar- 39 Ar method did not provide a spectra that could be interpreted unambiguously. A 40 Ar- 39 Ar plateau date of 76.9 ? 0.5 Ma from biotite phenocrysts in the lamprophyre indciates intrusion of mafic magma and attendant CO 2 metasomatism in the Late Cretaceous. Fission-track data from zircon in the rhyolite are permissive of slow uplift of the Belt Supergroup strata, 1U.S. Geological Survey, Box 25046, Denver Federal Center, Denver, CO 80225. 2Golden Sunlight Mines, Inc., 453 MT Highway 2 East, Whitehall, MT 59759. rhyolite, and lamprophyre between 55 and 50 Ma, but the data are not definitive. Rhyolitic welded tuff in the informally named units 7, 9, and 11 of the Elkhorn Mountains Volcanics is most similar in chemistry and age to the rhyolite at the Golden Sunlight mine. Trachybasalt in the Adel Mountains Volcanics and andesitic basalt in the informally named unit 8 of the Elkhorn Mountains Volcanics are the most analogous in chemistry and age to lamprophyres at the mine. The rhyolitic rocks appear to be derived from deep crustal sources, but data for the lamprophyres and mafic rocks in the Elkhorn Mountains Volcanics indicate that they were derived from the mantle.

Bulletin↗
USGS1989

Pb-Bi-Ag-Cu-(Hg) chemistry of galena and some associated sulfosalts. A review and some new data from Colorado California and Pennsylvania

Galena, associated with Pb-Bi-Ag sulfosalts and simple sulfides, contains varied amounts of Ag and Bi in the Dandy vein system, Idarado mine, Ouray, Colorado; the Jackass mine, Darwin District, California; and the Leadville district, Colorado. Silver- and bismuth-bearing galena associated with minor amounts of pyrite, chalcopyrite and sphalerite occur at the Pequea mine, Lancaster County, Pennsylvania. Ag and Bi contents in the Dandy suite of galena range from about 1.4 to 3.4 and 2.5 to 6.5 wt.% respectively, and are comparable or lower in galena from the other localities. Exsolved matildite is present in galena from the Dandy, Jackass and Leadville localities. The presence in significant amounts of both Ag and Bi in a Pb-rich sulfide system is necessary for formation of PbSss (galena solid-solution). If Ag (especially) and Bi (to a lesser extent) are absent, the galena formed will be essentially pure PbS. Some minor Sb may substitute for Bi. Compositional data for all of the galena samples are in agreement with a previously proposed linear relationship between a and Ag-Bi(Sb) content. Matildite and seven additional Pb-Bi-Ag-Cu sulfosalts have been identified from the Dandy vein system, based on electron-microprobe analyses and some X-ray powder-diffraction data.

Canadian Mineralogist↗
USGS1987

Shocked quartz in the Cretaceous-Tertiary boundary clays: Evidence for a global distribution

Shocked quartz grains displaying planar features were isolated from Cretaceous- Tertiary boundary clays at five sites in Europe, a core from the north-central Pacific Ocean, and a site in New Zealand. At all of these sites, the planar features in the shocked quartz can be indexed to rational crystallographic planes of the quartz lattice. The grains display streaking indicative of shock in x-ray diffraction photographs and also show reduced refractive indices. These characteristic features of shocked quartz at several sites worldwide confirm that an impact event at the Cretaceous-Tertiary boundary distributed ejecta products in an earth-girdling dust cloud, as postulated by the Alvarez impact hypothesis.

Science↗
USGS1986

Zimbabweite, a new alkali-lead arsenic tantalate from St Anns mine, Karoi district, Zimbabwe

Zimbabweite (Na,K) 2 PbAs 4 (Ta,Nb,Ti) 4 O 18 , a new mineral with trivalent arsenic, has been recognized at St Anns mine, southeast of Miami, Karoi district, Zimbabwe, in kaolinized pegmatite and dump material. The mineral is honey yellow-brown in large crystals, which are as much as 1 x 1 x 2 cm, and is clear pale yellow in thin fragments. Oxidation results in darkening of the color. There is one excellent cleavage, {010}. Zimbabweite has a Mohs hardness of 5 to 5.5, a white streak, adamantine luster, brittle fracture, is not magnetic, and does not fluoresce under either short wave or long wave ultraviolet light. d m = 6.20(3) and d c = 6.16 g/cm3. Optically, the mineral is biaxial (+), 2V Z = about 80°. Mean reflectances in air for an {010} = X-Z cleavage plate are : 589 nm--16.6 %, 470 nm--17.7 %, 546 nm--17.1 %, 650 nm--16.4 %. The indices of refraction determined by immersion methods are all greater than 2.10. Optic axis dispersion is very strong with ν > r, a = Z, b = Y, and c = X. The mineral is very pale yelow and is moderately pleochroic and X = pale yellow brown, Y = light reddish brown, and Z =reddish brown. Zimbabweite is insoluble in common acids or bases. A chemical analysis yielded, in weight percent, Ta 2 O 5 46.5, As 2 O 3 26.5, PbO 15.0, Nb 2 O 5 4.8, Na 2 O 3.1, K 2 O 1.5, TiO 2 1.4, BaO 0.4, UO 2 0.3, Bi 2 O 3 0.2, H 2 O (total) 0.19, SnO 2 0.1, F 0.04, SrO 0.02, total 100.05. A calculated formula is : (Na 1.51 K 0.48 Ba 0.04 ) Σ2.03 Pb 1.01 (As 4.03 Bi 0.01 ) Σ4.04 (Ta 3.17 Nb 0.55 Ti 0.26 U 0.02 Sn 0.01 ) Σ4.01 O 18 . Zimbabweite is orthorhombic, space group is Ccma or Cc2a , with a = 12.233(2)Å, b = 15.292(2)Å, c = 8.665(2)Å, V = 1621. 0(4) Å 3 , with Z = 4. No structural relationship between zimbabweite and any other tantalate minerals is apparent.

Karoi District↗