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J.S. Huebner

Publications and source records attributed to J.S. Huebner.

17 recordsLinked to original sources
USGS1995

Heat capacities and thermodynamic properties of braunite (Mn7 SiO12) and rhodonite (MnSiO3)

The heat capacities, C0P, of synthetic rhodonite and braunite have been measured by adiabatic calorimetry from 6 to ~350 K. The heat capacity of braunite was also measured to ~900 K by differential scanning calorimetry. Brunite exhibits a ??-peak in C0P in the temperature region 93.4-94.2 K. Rhodonite did not show the expected peak in C0P characteristic of the co-operative ordering of the Mn2+ spins at temperatures above 6 K. A revised petrogenetic grid for the system Mn-Si-O-C at 2000 bars is presented and is consistent with both thermochemical values and occurrence of natural assemblages. -from Authors

American Mineralogist↗
USGS1995

Impedance spectra of hot, dry silicate minerals and rocks: qualitative interpretation of spectra

Impedance spectroscopy helps distinguish the contributions that grain interiors and grain boundaries make to electrical resistance of silicate minerals and rocks. Olivine, orthopyroxene, clinopyroxenes, and both natural and synthetic clinopyroxenite were measured. A network of electrical elements is presented for use in interpreting impedance spectra and conductive paths in hot or cold, wet or dry, minerals and rocks at any pressure. In dry rocks, a series network path predominates; in wet rocks, aqueous pore fluid and crystals both conduct. Finite resistance across the sample-electrode interface is evidence that electronic charge carriers are present at the surface, and presumably within, the silicate minerals and rocks measured. -from Authors

American Mineralogist↗
USGS1992

Chemical fluxes and origin of a manganese carbonate-oxide-silicate deposit in bedded chert

Lens-like rhodochrosite-rich bodies within interbedded chert and shale are associated with basalt and/or graywacke in ophiolitic and orogenic zones. The Buckeye manganese mine in the Franciscan Complex of the California Coast Ranges is associated with metagraywacke. Despite blueschist-facies metamorphism, this deposit preserves the compositions and some textural features of its sedimentary protoliths. For this reason, it is a suitable deposit with which to compare more intensely altered deposits, or deposits originating in different paleoenvironments. Six Mn-rich and three Mn-poor minerals form monomineralic layers and mixtures: rhodochrosite, gageite, Mn-oxides (hausmannite, braunite), divalent Mn-silicates (caryopilite, taneyamalite), chlorite, quartz (metachert) and aegirine-augite. The Mn-rich protoliths have high Mn/Fe combined with relatively low concentrations of Ca, Al, Ti, Co, Ni, Cu, Th and REE. REE patterns of various protoliths are distinct. Rhodochrosite and gageite layers are depleted (seawater ?? 5 ?? 104) and flat, whereas patterns of metachert and the Mn-silicate-rich layers mimic the patterns of metashale and metagraywacke (seawater ?? 106). Hausmannite layers have flat patterns (seawater ?? 7 ?? 104) whereas braunite-rich layers are more enriched (seawater ?? 2 ?? 105) and show a distinct positive Ce anomaly. Factor analysis reveals components and fluxes attributed to sub-seafloor fluids (Ni, As, Zn, Sb, W, Mn), seawater (Mg, Au, V, Mo), detritus and veins (Ca, Ba, Sr). Silica is negatively correlated with the sub-seafloor factor. The observed variances indicate that water from the sediment column mixed with seawater, that deposition occurred near the sediment-seawater interface before mixtures of subsurface fluid and seawater homogenized, and that the system was not entirely closed during metamorphism. The variations in REE enrichment can be related to kinetics of deposition: rhodochrosite and gageite were precipitated most rapidly, and therefore were the protoliths that most effectively diluted the REE-rich background resulting from fine clastic material (derived from distal turbidites). The variation of the Ce anomaly and U/Th among diverse lithologies and the differences in Mn oxidation states are consistent with progressive dilution of reduced subsurface fluids with oxidized seawater. By this scheme, rhodochrosite, gageite and hausmannite were deposited from the most reduced fluids, braunite from intermediate mixtures, and Mn-silicates from the sub-seafloor fluids most diluted with fresh seawater. Comparison of the Buckeye with other lens-like and sheet-like deposits having high Mn/Fe and containing Mn3+ and/or Mn2+ suggests that each had three essential fluxes: a sub-seafloor source of Mn, a local source of very soluble silica and a source of relatively fresh, oxygenated water. Additional fluxes, such as clastics, appear to be more characteristic of the paleoenvironment than the three essential fluxes. ?? 1992.

Chemical Geology↗
USGS1992

Mineralogy and geochemistry of two metamorphosed sedimentary manganese deposits, Sierra Nevada, California, USA

Laminated to massive rhodochrosite, hausmannite, and Mn-silicates from the Smith prospect and Manga-Chrome mine, Sierra Nevada, California were deposited as ocean floor sediments associated with chert and shale. The principal lithologies at Smith are chert, argillite, rhodochrosite-, hausmannite- and chlorite-rich layers, and relatively uncommon layers of jacobsite. The Manga-Chrome mine also contains layers rich in manganoan calcite and caryopilite. Tephroite, rhodonite, spessartine, and accessory alleghanyite and sonolite formed during metamorphism. Volcaniclastic components are present at Manga-Chrome as metavolcanic clasts and as Mn-poor, red, garnet- and hematite-rich layers. There is no evidence, such as relict lithologies, that Mn was introduced into Mn-poor lithologies such as chert, limestone or mudstone. Replacement of Mn-poor phases by Mn-rich phases is observed only in the groundmass of volcanic clasts that appear to have fallen into soft Mn-rich mud. Manganiferous samples from the Smith prospect and Manga-Chrome mine have high Mn Fe and low concentrations of Ni, Cu, Zn, Co, U, Th and the rare-earth elements that are similar to concentrations reported from other ancient Mn deposits found in chert-greenstone complexes and from manganiferous sediments and crusts that are forming near modern sea floor vents. The Sierra Nevada deposits formed as precipitates of Mn-rich sediments on the sea floor, probably from mixtures of circulating hydrothermal fluids and seawater. The composition of a metabasalt from the Smith prospect is consistent with those of island-arc tholeiites. Metavolcanic clasts from the Manga-Chrome mine are compositionally distinct from the Smith metabasalt and have alkaline to calc-alkaline affinities. A back-arc basin is considered to be the most likely paleoenvironment for the formation of the Mn-rich lenses at the Manga-Chrome mine and, by association, the Smith prospect. Layers of rhodochrosite, hausmannite and chert preserve the composition and some textures of the sedimentary protoliths at both Sierra Nevada deposits. Jacobsite-rich layers probably represent a Fe-rich protolith. Caryopilite and manganoan calcite represent additional protoliths at the Manga-Chrome mine. The metamorphic assemblage prehnite-chlorite-epidote-calcite in a metabasalt from the Smith prospect constrains regional metamorphic conditions to a maximum temperature of 325??C and a pressure of 2 kbar. Slightly higher temperatures are indicated by the presence of actinolite in another metabasalt. Compositions of Mn-rich minerals in Smith samples are consistent with these metamorphic conditions. ?? 1992.

LITHOS↗
USGS1988

Electrical conductivity of diopside: evidence for oxygen vacancies

Impedance spectra for two natural single crystals of diopside were obtained at 800 to 1300??C and 1-bar pressure over the frequency range 0.001 Hz to 100 kHz in a system closed to all components but oxygen. At both higher and lower fO2 values, no fO2 dependence of conductivity was observed, indicating the presence of different conduction mechanisms. At temperatures less than 1000??C, the activation energy is 1.3 eV, also suggesting a different conduction mechanism. Thus, at least four regimes are necessary to describe the conductivity of this diopside in T-fO2 space. The approximately -1/(7 ?? 1) value of d(log ??)/d(log fO2) in a high-temperature geologic region suggests a reaction by which oxygen vacancies control the conductivity. This relatively pure diopside is much less conducting than olivine or orthopyroxene. A second diopside with greater Fe content but otherwise similar in composition to the near-end-member diopside, is more conducting, has a smaller activation energy (1.0 eV) over the range 1050 to 1225??C, and shows only a weak negative fO2 dependence; suggesting that oxygen vacancies are present but are not the dominant defect in controlling the conductivity. -from Authors

American Mineralogist↗
USGS1987

Conodont color and textural alteration: An index to regional metamorphism, contact metamorphism, and hydrothermal alteration

Experimental and field data are used to extend the utility of conodonts as semi-quantitative thermal indices into the regimes of regional and contact metamorphism, as well as hydrothermal alteration. An Arrhenius plot of data from induced conodont color alteration by pyrolysis in air at 1 atm was used to generate the geologic temperatures for conodont color-alteration indices (CAI) above 300 °C, that is, for CAI values of 5½ through 8. Such CAI values occur in very low- to medium-grade, regionally metamorphosed, contact-metamorphosed, and hydrothermally altered rocks. The uniformity or variability of CAI values within a sample, together with conodont texture, can help to distinguish grades and environments of metamorphism, particularly in metacarbonate sequences. Induced CAI by pyrolysis in a water-methane mixture at ½ kbar results in retardation of CAI and in a disparate mixture of both low and high CAI values within each experimental sample. In this system, color-alteration processes, above a CAI of 2 to 3, seem to change from predominantly carbonization to predominantly loss of organic matter, presumably by oxidation and volatilization of oxides. These experiments approximate the type of CAI mixture characteristically found in conodonts recovered from hydrothermally altered rocks. These data indicate that CAI values of 6 to 8 cannot be used to assess precise temperatures of hydrothermally altered rocks but may serve as useful indicators of potential mineralization.

Geological Society of America Bulletin↗
USGS1986

Nature of phases synthesized along the join (Mg,Mn)2Si2O6.

Eight compositions were synthesized along this join. Orthopyroxene crystallized at X = Mn/(Mn + Mg) = 0.0-0.3, clinopyroxene at X 0.4-0.5, and pyroxmangite at X 0.65-1.0, consistent with the composition ranges that have been inferred by examination of metamorphic rock assemblages. Unit-cell dimensions for these phases and for rhodonite (X = 1.0) are presented, along with microprobe chemical analyses and phase diagrams.-J.A.Z.

American Mineralogist↗
USGS1985

Dissolution of olivine in basaltic liquids: experimental observations and applications.

Rates of olivine dissolution in synthetic lunar basalt 77115 and a silica-enriched 77115 composition (Sil-77115) at superliquidus temperatures have been determined. Dissolution-rate data have been applied to the problem of the thermal history of fragment-laden impact-melt rocks of the lunar highlands. Textural and chemical criteria are discussed for the recognition of olivine resorption (and growth) phenomena in igneous rocks. -J.A.Z.

American Mineralogist↗
USGS1982

Techniques for using iron crucibles in experimental igneous petrology.

Some iron crucibles contain impurities of Mn, Ti and other elements. Such impurities may alter the fO2 of the system and induce crucible-charge interactions. Pretreatment of impure iron crucibles in a CO2-CO atmosphere at 1050oC, under conditions slightly more reducing than Fe-Fe1-xO, minimizes undesirable changes in the bulk composition of the charge. -J.A.Z.

American Mineralogist↗
USGS1970

Crystallography of some lunar plagioclases

Crystals of calcic bytownite from type B rocks have space group I1 with c ≈ 14 angstroms. Bytownite crystals from type A rocks are more sodic and have space group C1, c ≈ 7 angstroms. Cell parameters of eight bulk feldspar separates from crystalline rocks indicate that the range of angle gamma is about 23 times the standard error of measurement, and its value might be useful for estimation of composition. Cell parameters of seven ilmenites are close to those of pure FeTiO 3 .

Science↗