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F.E. Lichte

Publications and source records attributed to F.E. Lichte.

At least 19 recordsLinked to original sources
USGS2018

Proposed nomenclature for samarskite-group minerals: new data on ishikawaite and calciosamarskite

The current definition of samarskite-group minerals suggests that ishikawaite is a uranium rich variety of samarskite whereas calciosamarskite is a calcium rich variety of samarskite. Because these minerals are chemically complex, usually completely metamict, and pervasively altered, their crystal chemistry and structure are poorly understood. Warner and Ewing (1993) proposed that samarskite is an A 3+ B 5+ O 4 mineral with an atomic arrangement related to α-PbO 2 . X-ray diffraction analyses of the recrystallized type specimen of ishikawaite and the Ca-rich samarskite reveal that they have the same structure as samarskite-(Y) recrystallized at high temperatures. Electron microprobe analyses show that the only significant difference between samarskite-(Y), ishikawaite, and calciosamarskite lies in the occupancy of the A -site. The A -site of samarskite-(Y) is dominated by Y+ REE whereas the A -site of ishikawaite is dominantly U+Th and calciosamarskite is dominantly Ca. Additionally, a comparison of these data to those of Warner and Ewing (1993) show that in several cases Fe 2+ or Fe 3+ are dominant in the A -site. We propose that the name samarskite-( REE +Y) should be used when one of these elements is dominant and that the mineral be named with the most abundant of these elements as a suffix. The name ishikawaite should be used only when U+Th are dominant and the name calciosamarskite should only be used when Ca is the dominant cation at the A -site. Finally, because of the inability to quantify the valence state of iron in these minerals, the exact nature of the valence state of iron in these minerals could not be determined in this study.

Mineralogical Magazine↗
USGS2007

Determination of elements in National Bureau of Standards' geological reference materials SRM 278 obsidian and SRM 688 basalt by inductively coupled argon plasma-atomic emission spectrometry

Two new geologic reference materials, issued by the National Bureau of Standards as standard reference materials, have been analyzed by a precise, accurate, and rapid method of analysis for their element content. The described procedure uses a multi‐acid, low temperature digestion in a closed teflon vessel, followed by the simultaneous determination of 50 elements by inductively coupled argon plasma‐optical emission spectrometry. A preconcentration procedure was applied to a separate digestion for the accurate and precise determination of the rare earth elements. Average concentrations of 39 elements for SRM 278 obsidian and 36 elements for SRM 688 basalt are reported. The results for most elements are in good agreement with the certified values and those reported in the literature. Data for as many as 12 elements are reported for these samples for the first time.

Geostandards Newsletter↗
USGS2002

Determination of elemental content off rocks by laser ablation inductively coupled plasma mass spectrometry

A new method of analysis for rocks and soils is presented using laser ablation inductively coupled plasma mass spectrometry. It is based on a lithium borate fusion and the free-running mode of a Nd/YAG laser. An Ar/N2 sample gas improves sensitivity 7 ?? for most elements. Sixty-three elements are characterized for the fusion, and 49 elements can be quantified. Internal standards and isotopic spikes ensure accurate results. Limits of detection are 0.01 ??g/g for many trace elements. Accuracy approaches 5% for all elements. A new quality assurance procedure is presented that uses fundamental parameters to test relative response factors for the calibration.

Analytical Chemistry↗
USGS2002

Determination of the rare-earth elements in geological materials by inductively coupled plasma mass spectrometry

A method of analysis of geological materials for the determination of the rare-earth elements using the Inductively coupled plasma mass spectrometric technique (ICP-MS) has been developed. Instrumental parameters and factors affecting analytical results have been first studied and then optimized. Samples are analyzed directly following an acid digestion, without the need for separation or preconcentration with limits of detection of 2-11 ng/g, precision of ?? 2.5% relative standard deviation, and accuracy comparable to inductively coupled plasma emission spectrometry and instrumental neutron activation analysis. A commercially available ICP-MS instrument is used with modifications to the sample introduction system, torch, and sampler orifice to reduce the effects of high salt content of sample solutions prepared from geologic materials. Corrections for isobaric interferences from oxide ions and other diatomic and triatomic ions are made mathematically. Special internal standard procedures are used to compensate for drift in metahmetal oxide ratios and sensitivity. Reference standard values are used to verify the accuracy and utility of the method.

Analytical Chemistry↗
USGS2002

Determination of rare earth elements in geological materials by inductively coupled argon plasma/atomic emission spectrometry

Inductively coupled argon plasma/optical emission spectrometery (ICAP/OES) is useful as a simultaneous, multielement analytical technique for the determination of trace elements in geological materials. A method for the determination of trace-level rare earth elements (REE) in geological materials using an ICAP 63-channel emission spectrometer is described. Separation and preconcentration of the REE and yttrium from a sample digest are achieved by a nitric acid gradient cation exchange and hydrochloric acid anion exchange. Precision of 1-4% relative standard deviation and comparable accuracy are demonstrated by the triplicate analysis of three splits of BCR-1 and BHVO-1. Analyses of other geological materials including coals, soils, and rocks show comparable precision and accuracy.

Analytical Chemistry↗
USGS1999

Simmonsite, Na2LiAlF6, a new mineral from the Zapot amazonite-topazzinnwaldite pegmatite, Hawthorne, Nevada, U.S.A

Simmonsite, Na2LiAlF6, a new mineral of pegmatitic-hydrothermal origin, occurs in a late-stage breccia pipe structure that cuts the Zapot amazonite-topaz-zinnvvaldite pegmatite located in the Gillis Range, Mineral Co., Nevada, U.S.A. The mineral is intimately intergrown with cryolite, cryolithionite and trace elpasolite. A secondary assemblage of other alumino-fluoride minerals and a second generation of cryolithionite has formed from the primary assemblage. The mineral is monoclinic, P21 or P21/m, a = 7.5006(6) A??, b = 7.474(1) A??, c = 7.503(1) A??, ??= 90.847(9) ??, V=420.6(1) A??3, Z = 4. The four strongest diffraction maxima [d(A??), likl, I/I100] are (4.33, 111 and 111, 100); (1.877, 400 and 004, 90); (2.25, 13T, 113, 131 and 311, 70); and (2.65, 220, 202, 022, 60). Simmonsite is pale buff cream with white streak, somewhat greasy, translucent to transparent, Mohs hardness of 2.5-3, no distinct cleavage, subconchoidal fracture, no parting, not extremely brittle, Dm is 3.05(2) g/cm3, and Dc is 3.06(1) g/cm3. The mineral is biaxial, very nearly Isotropie, N is 1.359(1) for ?? = 589 nm, and birefringence is 0.0009. Electron microprobe analyses gave (wt%) Na = 23.4, Al = 13.9, F = 58.6, Li = 3.56 (calculated), with a total of 99.46. The empirical formula (based on 6 F atoms) is Na1.98Li1.00 ooAl|ooF6. The crystal structure was not solved, presumably because of unit-cell scale twinning, but similarities to the perovskite-type structure exist. The mineral is named for William B. Simmons, Professor of Mineralogy and Petrology, University of New Orleans, New Orleans.

American Mineralogist↗
USGS1997

The chemical evolution and paragenesis of uranium minerals from the ruggles and palermo granitic pegmatites, New Hampshire

A study of the chemical evolution and paragenesis of the uranium minerals at the Palermo No. 1 and Ruggles granitic pegmatites, Grafton County, New Hampshire, revealed four stages of secondary mineralization. A total of eight uranium minerals were identified in the four stages. The first stage is a mixture of uranyl oxide hydroxide-hydrates represented by mineral "A", which surrounds and replaces a uraninite core. The second stage is a carbonate stage found only at the Palermo No. 1 pegmatite, and is represented by rutherfordine. The third stage is represented by uranyl silicates. At the Palermo No. 1 pegmatite, this stage consists of ??-uranophane, and at the Ruggles pegmatite, it consists of soddyite and ??-uranophane. A final fourth stage is a phosphate stage represented by phosphuranylite and meta-autunite I. The first three stages of mineralization developed from hydrothermal and meteoric processes. With dropping temperatures, hydrothermal fluids reached meteoric temperatures and acquired the characteristics of meteoric water. The pH shifted from acidic (pH less than about 6 at 100??C) to alkaline (pH > 7 at 25??C). Since mineral "A" contains hydroxyl and a low amount of molecular water, it probably formed at a temperature greater than 100??C in the acidic environment. After the first stage, the hydrothermal fluids likely reached the temperatures of meteoric water. The initial pH of the meteoric water was acidic (pH less than about 6 at 25??C) and then slowly shifted to alkaline. The mineralizing fluids became oversaturated in CO3, Ca, K, and Si. Uraninite and mineral "A" became unstable and were replaced by rutherfordine and uranyl silicates. The fourth or phosphate stage developed from the introduction of groundwater. The uranyl phosphate minerals precipitated from an acidic fluid (pH < 7 at 25??C) that was oversaturated with Ca, K, U, and P.

Canadian Mineralogist↗
USGS1997

Additional studies on mixed uranyl oxide-hydroxide hydrate alteration products of uraninite from the palermo and ruggles granitic pegmatites, grafton county, New Hampshire

Additional studies on an incompletely characterized secondary uranium "mineral" from the Ruggles and Palermo granitic pegmatites, New Hampshire, referred to as mineral "A" by Frondel (1956), reveal a mixture of schoepite-group minerals and related uranyl oxide-hydroxide hydrated compounds. A composite chemical analysis yielded (in wt.%): PbO 4.85 (EMP), UO3 83.5 (EMP), BaO 0.675 (av. of EMP and ICP), CaO 0.167 (av. of EMP and ICP), K2O 2.455 (av. of EMP and ICP), SrO 0.21 (ICP), ThO2 0.85 (ICP), H2O 6.9, ??99.61. Powder-diffraction X-ray studies indicate a close resemblance in patterns between mineral "A" and several uranyl oxide-hydroxide hydrated minerals, including the schoepite family of minerals and UO2(OH)2. The powder-diffraction data for mineral "A" are most similar to those for synthetic UO2.86??1.5H2O and UO2(OH)2, but other phases are likely present as well. TGA analysis of both mineral "A" and metaschoepite show similar weight-loss and first derivative curves. The dominant losses are at 100??C, with secondary events at 400?? and 600??C. IR spectra show the presence of (OH) and H2O. Uraninite from both pegmatites, analyzed by LAM-ICP-MS, shows the presence of Th, Pb, K and Ca.

Canadian Mineralogist↗
USGS1996

Li- and F-bearing alkali amphibole from granitic pegmatite at Hurricane Mountain, Carroll County, New Hampshire

At Hurricane Mountain, Carroll County, New Hampshire, bodies of granitic pegmatite in riebeckite granite contain large (up to 10 cm long and 2 cm across) primary crystals of Li-bearing fluor-arfvedsonite in miarolitic cavities, grading to euhedral Li- and F-poor arfvedsonite. Fine-grained, fibrous, light blue-gray riebeckite occurs as a late-stage hydrothermal filling in the miarolitic cavities. The early, Li-rich, fluor-arfvedsonite has: a 9.836(5), b 17.997(7), c 5.316(4) A??, ?? 103.735(4)??, V 914.20(6) A??3; Z = 2, Dmeas. 3.34 g/cm3, Dcalc. 3.353 g/cm3; biaxial (-), 2Vmeas. 44(1)??, 2Vcalc. 46??; ?? 1.681(2), ?? 1.692(2), ?? 1.694(2), inclined dispersion, r > v; X ??? c -7??, Y = b, Z ??? a +7??; X dark blue, Y lavender gray, Z pale yellowish brown; X > Y > Z; X is opaque at 0.03 mm thickness. A structural formula, on the basis of 24 (O,OH,F) atoms is: (Na0.86K0.25)Na2(Fe2+2.54Fe3+1.485Mn0.10Zn 0.02Li0.49Ti0.07)(Si7.71Al 0.07)O22(F1.34OH0.63). Arfvedsonite within the miarolitic cavities contains less Li and F than that of the earlier generation, and the still later riebeckite contains only 0.09 wt.% Li2O and 0.3 wt.% F. The Fe3+:Fe2+ ratio of the early Li-bearing fluor-arfvedsonite and that of the euhedral arfvedsonite crystals within miarolitic cavities is 0.58. The late, fibrous, cavity-filling riebeckite has an Fe3+:Fe2+ ratio of 0.99. The total iron content of the three amphiboles increases with continued crystallization. These amphiboles are products of peralkaline pegmatites locally derived from peralkaline granite.

Canadian Mineralogist↗
USGS1996

Paragenetic and minor- and trace-element studies of Mississippi Valley-type ore deposits of the Silesian-Cracow district, Poland

Paragenetic and minor- and trace-element studies were conducted on samples of epigenetic ore and gangue minerals collected from mines and drill core in the Silesian-Cracow (S-C) district of southern Poland. Four discrete mineral suites representing four mineralizing stages can be identified throughout the district. The earliest epigenetic minerals deposited during stage 1 consist of a late dolomite cement together with minor pyrite and marcasite. Stage 2 was the first ore-forming stage and included repetitive deposition of sphalerite and galena in a variety of morphologies. Stage 3 abruptly followed the first ore stage and deposited marcasite and pyrite with variable amounts of late sphalerite and galena. In the samples studied, minerals deposited during stage 3 are predominately marcasite-pyrite with minor sphalerite and galena in the Pomorzany and Olkusz mines, whereas, at the Trzebionka mine, stage 3 mineralization deposited mostly galena and sphalerite with little marcasite or pyrite. Stage 4 minerals include contains barite, followed by calcite, with very minor pyrite and a rare, late granular sphalerite. Compared to other major Mississippi Valley-type (MVT) districts of the world, the Silesian-Cracow district contains sphalerite with the second largest range in Ag concentrations and the largest range in Fe and Cd concentrations of any district. Unlike in other districts, very wide ranges in minor- and trace-element concentrations are also observed in paragenetically equivalent samples collected throughout the district. This wide range indicates that the minor- and trace-element content of the ore-forming environment was highly variable, both spatially and temporally, and suggests that the hydrologic system that the ore fluids traversed from their basinal source was very complex. Throughout the district, a significant increase in Tl, Ge, and As concentrations is accompanied by a lightening of sulfur isotopes between stage 2 and stage 3 minerals. This change appears to record a major district-scale hydrologic event that probably reflects the introduction of fluids with significantly different geochemistry than that of earlier ore-forming fluids.

Prace - Panstwowego Instytutu Geologicznego↗
USGS1995

A new U-Ti-Ca-HREE hydrated oxide and associated niobian rutile from Topaz Valley, Utah

In October of 1988, specimens of yellow and/or white acicular needles growing out of equant to platy hematite were collected from the east side of Topaz Valley. For the past five years, attempts have been made by all of the authors to completely characterize what is believed to be a new mineral species. Because of several major factors the space group, exact formula, and structure are still unknown. The potentially new mineral and some associated minerals are described here with the hope that elsewhere in the world better and more material exists that will allow complete characterization. -from Authors

Mineralogical Record↗
USGS1995

Pink topaz from the Thomas Range, Juab County, Utah

The Thomas Range is world-famous for its production of topaz Al2SiO4(F,OH)2, occurring in lithophysal cavities in rhyolite. Topaz Valley, at the southern end of the range, is perhaps the single most famous locality. While fine-quality, sherry-orange crystals to 5 cm or more in length occur at various localities, pale to medium pink crystals were first reported from the Thomas Range in 1934. The cause of the unusual coloration, unknown for 60 years, is now believed to be substitution of Mn3+ ?? Fe3+ for Al3+. -Authors

Mineralogical Record↗
USGS1995

The biogeochemistry of wetlands in the San Luis Valley, Colorado: The effects of acid drainage from natural and mine sources

The Summitville Mine, located near the old mining town of Summitville in Rio Grande County, Colorado, operated between July 1986 and December 1992 as a large-tonnage open-pit heap-leach gold mine. During its 6 years of existence the trace metal levels in drainage water from the mine site were elevated over historical (pre-1986) levels (Moran and Wentz, 1974) due to input from three sources—heap leach water, seeps that occur throughout the mine workings, and an increase in the metal load of water coming from the old Reynolds Adit. Mine-drainage waters flow into Wightman Fork, a small tributary of the Alamosa River, which in turn flows east into the San Luis Valley. The increase in the trace metal burden of the Alamosa River watershed is of concern to farmers, land owners, and Federal and State wildlife agencies. The information presented here is largely abstracted from reports previously published (Balistrieri and others, 1995; Gough and others, 1995).

Colorado↗
USGS1994

McCrillisite, NaCs(Be,Li)Zr2(PO4)4.1-2H2O, a new mineral species from Mount Mica, Oxford County, Maine, and new data for gainesite

McCrillisite, a member of the gainesite group, occurs in the Mount Mica granitic pegmatite, South Paris, Oxford County, Maine. The mineral is a product of late-stage hydrothermal alteration and is associated with approximately 20 other silicate, oxide, carbonate, arsenite and phosphate minerals. Crystals occur in mm- to cm-sized cavities, and individuals are up to 1.2 mm in maximum dimension. The crystallography and mineral chemistry of McCrillisite are described. -from Authors

Canadian Mineralogist↗
USGS1994

Plumboan crichtonite: from the Fazenda Guariba, Minas Gerais, Brazil

Senaite, Pb(Ti,Fe,Mn)21O38, a member of the crichtonite group, was first described from alluvial gravels near Dattas, Minas Gerais, Brazil. It was subsequently reported (always from alluvial stream gravels) from about seven additional localities. "Senaite' from the first in situ source in Brazil, at the Fazenda Guariba, Minas Gerais, Brazil was described by Cassedanne (1988). Approximately 20 crystals of "senaite' from the Fazenda Guariba were examined chemically and all were found to be plumboan crichtonite rather than senaite. -from Authors

Mineralogical Record↗
USGS1993

Thortveitite and associated Sc-bearing minerals from Ravalli County, Montana

The rare Sc mineral thortveitite, (Sc,Y)2Si2O7, occurs as ??m- to mm-sized crystals in fluorite-bearing granitic pegmatites and the host melagabbro within the Crystal Mountain fluorite deposit, Ravalli County, Montana. Thortveitite is found as colorless and clear to smoky and translucent, subhedral to euhedral prisms up to 3 mm in length in the massive fluroite, as mm-sized anhedra to subhedra in diopside and edenite, and as ??m-sized droplet-like crystals in actinolite. Micrometric textures suggest that some thortveitite exsolved from actinolite, which contains between 1.2 and 2.9 wt.% Sc2O3. The source of the Sc is believed to be magmatic. The physical, optical and crystallographic properties of thortveitite are described. -from Authors

Canadian Mineralogist↗