Crystal chemical significance of chemical zoning in dissakisite-(Ce)

Dissakisites from Trimouns dolomite mine, France, have two kinds of single crystals: chemical-zoned and homogeneous types. Back-scattered electron microprobe (BSE) images of these dissakisites reveal both Ca–Al rich dark zones and Fe-ΣREE rich bright zones. Crystal structures of three dark and two bright zones in a chemical-zoned dissakisite and of a homogeneous zone in unzoned dissakisite were refined to individual R indices (about 3.0–5.0%) based on 1,400 observed [|F ₀| > 4σF ₀] reflections measured with MoKα X-radiation using the single crystal diffractometer. The differences in brightness between their BSE images arise from those in coupled substitutions of the elements occupying A2 and M3 sites. The main reason for these differences is that ten-coordinated A2 polyhedra and M3 octahedra are directly linked through their shared edge, which creates a great potential for making this coupled substitution. This zoning indicates that formation of the whole zoned crystal, where each zone could be grown steadily with its crystallographic axes mutually parallel to each other, may be identified as autoepitaxy.     

Finite difference analogue of the Coriolis force

It is shown by a numerical experiment with fine grid that the finite difference form of rotation of the Coriolis force used in ENDOH (1973) gives practically the same solution as that obtained by the use of the finite difference form pointed out byTakano (1974).     

Kosa (yellow sand) components in precipitation collected at central Japan

In east Asia, acidic gases derived from fossil fuel combustion have increased in the past decades. On the other hand, the Asian dust, also called Kosa (yellow sand) is transported following windstorms from arid lands in the Asian continent. Many researchers have been interested in the reaction between acidic aerosols and Kosa aerosols as well as the long-range transport of these emissions. To investigate the characteristics of chemical components in precipitation on a long-term basis over Japan, precipitation was sequentially collected from April 1984 to March 1997 at Kanazawa located near the coast of the Sea of Japan. Precipitation samples were collected at 1 mm intervals for the first 5 mm rainfall and all volume of rainwater after 6 mm for all precipitation events with an automatic wet only precipitation collector. According to the analyses of precipitation including Kosa aerosols during Kosa periods, the reaction in the air between Kosa and acidic components during the long-range transport was discussed.     

Near-infrared and Visible Light Microthermometry of Fluid Inclusions in Sphalerite from a Possible Southeast Extension of the Toyoha Polymetallic Deposit, Japan

Abstract. Near-infrared (NIR) and visible light microthermometry was applied to the fluid inclusions in sphalerite from a possible southeast extension of the Toyoha polymetallic deposit. Sphalerite occurs as euhedral-subhedral crystals or collo-form aggregates with a variety of color, which contain a well-developed growth banding. Combined with morphological observations, fluid inclusions in dark-colored sphalerite were examined using a near-infrared light microscopic technique, whereas those in light-colored sphalerite and quartz were examined by a conventional visible light microscopy.
Salinities of fluid inclusions in dark-colored sphalerite have a wide variation (1.0–10.3 wt % NaCl equiv.) compared to that in light-colored sphalerite and quartz (0.0–3.4 wt % NaCl equiv.). These variations suggest that the conventional microthermometric data from light-colored sphalerite and quartz were inadequate to interpret the ore formation process. Dark-colored colloform sphalerite and a dark core of subhedral sphalerite formed from high-salinity fluids (6.5–10.3 wt % NaCl equiv.) under highly supersaturated conditions with respect to sphalerite.
The NIR and visible light microthermometry of fluid inclusions in sphalerite combined with its morphological observations is an invaluable method to infer the formation conditions of sphalerite. The NIR and visible light microthermometry is useful to reveal how the nature of ore fluids changed with time.     

The effect of iron on montmorillonite stability. (I) Background and thermodynamic considerations

It is envisaged that high-level nuclear waste (HLW) will be disposed of in underground repositories. Many proposed repository designs include steel waste canisters and bentonite backfill. Natural analogues and experimental data indicate that the montmorillonite component of the backfill could react with steel corrosion products to produce non-swelling Fe-rich phyllosilicates such as chamosite, berthierine, or Fe-rich smectite. In K-bearing systems, the alteration of montmorillonite to illite/glauconite could also be envisaged. If montmorillonite were altered to non-swelling minerals, the swelling capacity and self-healing properties of the bentonite backfill could be reduced, thereby diminishing backfill performance. The main aim of this paper was to investigate Fe-rich phyllosilicate mineral stability at the canister-backfill interface using thermodynamic modelling. Estimates of thermodynamic properties were made for Fe-rich clay minerals in order to construct approximate phase-relations for end-member/simplified mineral compositions in logarithmic activity space. Logarithmic activity diagrams (for the system Al₂O₃-FeO-Fe₂O₃-MgO-Na₂O-SiO₂-H₂O) suggest that if pore waters are supersaturated with respect to magnetite in HLW repositories, Fe(II)-rich saponite is the most likely montmorillonite alteration product (if f_O2(g) values are significantly lower than magnetite-hematite equilibrium). Therefore, the alteration of montmorillonite may not be detrimental to nuclear waste repositories that include Fe, as long as the swelling behaviour of the Fe-rich smectite produced is maintained. If f_O2(g) exceeds magnetite-hematite equilibrium, and solutions are saturated with respect to magnetite in HLW repositories, berthierine is likely to be more stable than smectite minerals. The alteration of montmorillonite to berthierine could be detrimental to the performance of HLW repositories.     

Petrological,petrofabric, and oxygen isotopic study of five ungrouped meteorites related to brachinites

Northwest Africa (NWA) 6112, Miller Range (MIL) 090206 (plus its pairs: MIL 090340 and MIL 090405), and Divnoe are olivine‐rich ungrouped achondrites. We investigated and compared their petrography, mineralogy, and olivine fabrics. We additionally measured the oxygen isotopic compositions of NWA 6112. They show similar petrography, mineralogy, and oxygen isotopic compositions and we concluded that these five meteorites are brachinite clan meteorites. We found that NWA 6112 and Divnoe had a c axis concentration pattern of olivine fabrics using electron backscattered diffraction (EBSD). NWA 6112 and Divnoe are suggested to have been exposed to magmatic melt flows during their crystallization on their parent body. On the other hand, the three MIL meteorites have b axis concentration patterns of olivine fabrics. This indicates that the three MIL meteorites may be cumulates where compaction of olivine grains was dominant. Alternatively, they formed as residues and were exposed to olivine compaction. The presence of two different olivine fabric patterns implies that the parent body(s) of brachinite clan meteorites experienced diverse igneous processes.     

Cathodoluminescence of high-pressure feldspar minerals as a shock barometer

Cathodoluminescence (CL) analyses were carried out on maskelynite and lingunite in L6 chondrites of Tenham and Yamato-790729. Under CL microscopy, bright blue emission was observed in Na-lingunite in the shock veins. Dull blue-emitting maskelynite is adjacent to the shock veins, and aqua blue luminescent plagioclase lies farther away. CL spectroscopy of the Na-lingunite showed emission bands centered at ~330, 360–380, and ~590 nm. CL spectra of maskelynite consisted of emission bands at ~330 and ~380 nm. Only an emission band at 420 nm was recognized in crystalline plagioclase. Deconvolution of CL spectra from maskelynite successfully separated the UV–blue emission bands into Gaussian components at 3.88, 3.26, and 2.95 eV. For comparison, we prepared K-lingunite and experimentally shock-recovered feldspars at the known shock pressures of 11.1–41.2 GPa to measure CL spectra. Synthetic K-lingunite has similar UV–blue and characteristic yellow bands at ~550, ~660, ~720, ~750, and ~770 nm. The UV–blue emissions of shock-recovered feldspars and the diaplectic feldspar glasses show a good correlation between intensity and shock pressure after deconvolution. They may be assigned to pressure-induced defects in Si and Al octahedra and tetrahedra. The components at 3.88 and 3.26 eV were detectable in the lingunite, both of which may be caused by the defects in Si and Al octahedra, the same as maskelynite. CL of maskelynite and lingunite may be applicable to estimate shock pressure for feldspar-bearing meteorites, impactites, and samples returned by spacecraft mission, although we need to develop more as a reliable shock barometer.     

Mineralogical characterization of a unique material having heavy oxygen isotope anomaly in matrix of the primitive carbonaceous chondrite Acfer 094

We report the mineral compositions and micro-texture of the isotopically anomalous (δ^17,18O_SMOW ∼ +180‰) Fe-S-Ni-O material recently discovered in matrix of the primitive carbonaceous chondrite Acfer 094 [Sakamoto N., Seto Y., Itoh S., Kuramoto K., Fujino K., Nagashima K., Krot A. N. and Yurimoto H. (2007) Oxygen isotope evidence for remnants of the early solar system primordial water. Science317, 231-233]. Synchrotron radiation X-ray diffraction and transmission electron microscopy studies indicate that this material consists of the symplectitically intergrown magnetite (Fe₃O₄) and pentlandite (Fe_5.7Ni_3.3S₈) with magnetite/pentlandite volume ratio of ∼2.3. Magnetite forms column-shaped grains (10-30 nm in diameter and 100-200 nm in length); pentlandite occurs as worm-shaped grains or aggregates of grains 100-300 nm in size between magnetite crystals. Although both the X-ray diffraction and electron energy loss spectra support identification of iron oxide as magnetite, the electron diffraction patterns show that magnetite has a weak 3-fold superstructure, possibly due to ordering of vacancies. We infer that the isotopically anomalous symplectite formed by sulfurization and oxidization of metal grains either in the solar nebula or on an icy planetesimal. The intersite cation distribution of pentlandite suggests that timescale of oxidation was no longer than 1000 years.