Alkali (Rb/K) abundances in Allende barred-olivine chondrules: Implications for the melting conditions of chondrules

Abstract— In order to study abundances of alkali metals in chondrules, 25 petrographically characterized chondrules, including 18 barred olivine (BO) chondrules from the Allende (CV3) meteorite, were analyzed for alkalis (K and Rb) and alkaline earths (Sr, Ba, Ca and Mg) by mass spectrometric isotope dilution. Most BO chondrules with higher alkalis (>CI level) have nearly CI-chondritic Rb/K ratios, while those with lower alkalis clearly show higher Rb/K ratios than the CI-chondritic. In general, BO chondrules with higher Rb/K exhibit more depletion of alkalis relative to Ca. The mean olivine Fa for individual chondrules positively correlates with bulk alkali concentrations in BO type but not in porphyritic type chondrules. These observations suggest that some BO chondrules formed from more reducing assemblages of precursor minerals, which experienced more intensive vaporization losses of alkalis, accompanied by Rb/K fractionation, during the chondrule-formation melting.     

Maximal size of chondrules in shock wave heating model: Stripping of liquid surface in a hypersonic rarefied gas flow

Abstract— We examined partially molten dust particles that have a solid core and a surrounding liquid mantle, and estimated the maximal size of chondrules in a framework of the shock wave heating model for chondrule formation. First, we examined the dynamics of the liquid mantle by analytically solving the hydrodynamics equations for a core‐mantle structure via a linear approximation. We obtained the deformation, internal flow, pressure distribution in the liquid mantle, and the force acting on the solid core. Using these results, we estimated conditions in which liquid mantle is stripped off from the solid core. We found that when the particle radius is larger than about 1–2 mm, the stripping is expected to take place before the entire dust particle melts. So chondrules larger than about 1–2 mm are not likely to be formed by the shock wave heating mechanism. Also, we found that the stripping of the liquid mantle is more likely to occur than the fission of totally molten particles. Therefore, the maximal size of chondrules may be determined by the stripping of the liquid mantle from the partially molten dust particles in the shock waves. This maximal size is consistent with the sizes of natural chondrules.     

Distribution of gold and silver and its relation with hypogene ore minerals in the Esperanza porphyry deposit,Antofagasta Region,Chile

Modes of occurrence of Au‐ and Ag‐bearing phases and their relation with associated hypogene ore minerals were examined with the objective to elucidate Au‐Ag distribution at the Esperanza porphyry deposit in the Eocene Centinela copper belt, using ore‐microscope modal analysis, semi‐quantitative analyses by automated mineralogy, electron probe microanalysis, and secondary ion mass spectrometer. The Esperanza hypogene mineralization is characterized by early‐stage chalcopyrite‐rich veinlets in the potassic alteration zone and later polymetallic stage with tennantite and galena in the chlorite‐sericitic alteration zone. Only the early‐stage chalcopyrite contains fine‐grained electrum (Au₆₈Ag₃₂ ‐ Au₈₁Ag₁₉) and hessite (Ag₂Te), and thus yields positive correlations in Cu vs. Au and Cu vs. Ag grades that are clearly recognized in the hypogene sulfide zone. The early‐stage chalcopyrite grains frequently exhibit polysynthetic twinning suggestive of inversion from intermediate solid solution. These features suggest that the fine‐grained electrum and hessite are products exsolved in the cooling process with the intermediate solid solution to chalcopyrite inversion. In contrast, tennantite and galena of the later‐stage mineralization contain no detectable Ag, and it is thus proposed that the early‐stage inverted chalcopyrite is the principal storage of economically important precious metals.     

Petrogenesis of ultramafic rocks and olivine-rich troctolites from the East Taiwan Ophiolite in the Lichi mélange

Mineralogy and Petrology - We examine ultramafic and olivine-rich troctolite blocks of the East Taiwan Ophiolite (ETO) in the Lichi Mélange. Although ultramafic rocks are extensively...     

Coupled Simulation of Seismic Wave Propagation and Failure Phenomena by Use of an MPS Method

The failure of brittle materials, for example glasses and rock masses, is commonly observed to be discontinuous. It is, however, difficult to simulate these phenomena by use of conventional numerical simulation methods, for example the finite difference method or the finite element method, because of the presence of computational grids or elements artificially introduced before the simulation. It is, therefore, important for research on such discontinuous failures in science and engineering to analyze the phenomena seamlessly. This study deals with the coupled simulation of elastic wave propagation and failure phenomena by use of a moving particle semi-implicit (MPS) method. It is simple to model the objects of analysis because no grid or lattice structure is necessary. In addition, lack of a grid or lattice structure makes it simple to simulate large deformations and failure phenomena at the same time. We first compare analytical and MPS solutions by use of Lamb’s problem with different offset distances, material properties, and source frequencies. Our results show that analytical and numerical seismograms are in good agreement with each other for 20 particles in a minimum wavelength. Finally, we focus our attention on the Hopkinson effect as an example of failure induced by elastic wave propagation. In the application of the MPS, the algorithm is basically the same as in the previous calculation except for the introduction of a failure criterion. The failure criterion applied in this study is that particle connectivity must be disconnected when the distance between the particles exceeds a failure threshold. We applied the developed algorithm to a suspended specimen that was modeled as a long bar consisting of thousands of particles. A compressional wave in the bar is generated by an abrupt pressure change on one edge. The compressional wave propagates along the interior of the specimen and is visualized clearly. At the other end of the bar, the spalling of the bar is reproduced numerically, and a broken piece of the bar is formed and falls away from the main body of the bar. Consequently, these results show that the MPS method effectively reproduces wave propagation and failure phenomena at the same time.     

Geochemistry of spinel-hosted amphibole inclusions in abyssal peridotite: insight into secondary melt formation in melt–peridotite reaction

Spinel-hosted hydrous silicate mineral inclusions are often observed in dunite and troctolite as well as chromitite. Their origin has been expected as products associated with melt–peridotite reaction, based on the host rock origin. However, the systematics in mineralogical and geochemical features are not yet investigated totally. In this study, we report geochemical variations of the spinel-hosted pargasite inclusions in reacted harzburgite and olivine-rich troctolite collected from Atlantis Massif, an oceanic core complex, in the Mid-Atlantic Ridge. The studied samples are a good example to examine geochemical variations in the inclusions because the origin and geological background of the host rocks have been well constrained, such as the reaction between MORB melt and depleted residual harzburgite beneath the mid-ocean ridge spreading center. The trace-element compositions of the pargasite inclusions are characterized by not only high abundance of incompatible elements but also the LREE and HFSE enrichments. Distinctive trace-element partitioning between the pargasite inclusion and the host-rock clinopyroxene supports that the secondary melt instantaneously formed by the reaction is trapped in spinel and produces inclusion minerals. While the pargasite geochemical features can be interpreted by modal change reaction of residual harzburgite, such as combination of orthopyroxene decomposition and olivine precipitation, degree of the LREE enrichment as well as variation of HREE abundance is controlled by melt/rock ratio in the reaction. The spinel-hosted hydrous inclusion could be embedded evidence indicating melt–peridotite reaction even if reaction signatures in the host rock were hidden by other consequent reactions.     

Silica enrichment of Group II xenoliths by evolved alkali basalt from Jeju Island, South Korea: implication for modification of intraplate deep-seated rocks

Group II xenoliths, corresponding to the lithology of dunite, wehrlite to olivine clinopyroxenite and olivine websterite to websterite, occur in Pleisto-Holocene alkali basalts from Jeju Island, South Korea. The large grain size (up to 5?mm), moderate mg# [=100?×?Mg/(Mg?+?Fe_total) atomic ratio] of olivine (79–82) and pyroxenes (77–83), and absence of metamorphic textural features indicate that they are cumulates of igneous origin. Based on textural features, mineral equilibria and major and trace element variations, it can be inferred that the studied xenoliths were crystallized from basaltic melts enriched in incompatible trace elements and belong to the Jeju Pleisto-Holocene magma system. They appear to have been emplaced near the present Moho, an estimated 5–8?kbars beneath Jeju Island. Consolidation of cumulates was followed by infiltration of silica-enriched metasomatic melt, producing secondary orthopyroxenes at the expense of olivine. The metasomatic agent appears to have been a silica-enriched residual melt evolved from an initially slightly silica-undersaturated alkali basalt to silica-saturated compositions by fractional crystallization under relatively high pressure conditions. The result of this study indicates that relatively young olivine-bearing cumulates could have been metasomatized by a silica-enriched melt within underplates, suggesting that silica enrichment can occur in intraplate Moho-related rocks as well as in the upper mantle of the subarc area.     

Origin of wehrlite cumulates in the Moho transition zone of the Neoproterozoic Ras Salatit ophiolite,Central Eastern Desert,Egypt: crustal wehrlites with typical mantle characteristics

Ultramafic cumulates, mainly crustal true wehrlites, were discovered and described in the mantle–crust transition zone (MTZ) and the extremely lower layered gabbro sequence of the Ras Salatit ophiolite, Central Eastern Desert, Egypt. They form either boudinaged lensoidal tabular bodies or interdigitated layers often concordant with the planolinear fabrics of the Ras Salatit ophiolite rocks. The contact between wehrlites and the host MTZ dunite or layered gabbro is razor sharp, lobate and/or sinuous, without chilled margins or any visible deformations. The Ras Salatit wehrlites are orthopyroxene-free and composed mainly of olivine and clinopyroxene. They are texturally equilibrated and show a characteristic poikilitic texture. Crystallization order of the Ras Salatit wehrlites is olivine/spinel followed by clinopyroxene with the absence of plagioclase. Olivine and clinopyroxene of the Ras Salatit wehrlites are compositionally uniform and conspicuously high in Mg#, mostly around 0.93 and 0.92, respectively. Moreover, the clinopyroxene shows low Ti and Al contents coupled with marked depletion in LILE. The calculated melt in equilibrium with clinopyroxene from the Ras Salatit wehrlites is largely similar to lavas from the Izu-Bonin forearc. Given the above characteristics, the Ras Salatit wehrlites were produced by crystal accumulation from a hydrous depleted basaltic/tholeiitic melt corresponding to temperatures between 1,000 and 1,100°C at the oceanic crustal pressure (~2 kbar). The involved hydrous tholeiitic melt has been probably formed by fluid-assisted partial melting of a refractory mantle source (similar to the underlying harzburgites) in a somewhat shallow sub-arc environment.     

Structural changes of synthetic opal by heat treatment

The structural changes of synthetic opal by heat treatment up to 1,400 °C were investigated using scanning electron microscopy, X-ray diffraction, and Fourier transform infrared and Raman spectroscopies. The results indicate that the dehydration and condensation of silanol in opal are very important factors in the structural evolution of heat-treated synthetic opal. Synthetic opal releases water molecules and silanols by heat treatment up to 400 °C, where the dehydration of silanol may lead to the condensation of a new Si–O–Si network comprising a four-membered ring structure of SiO₄ tetrahedra, even at 400 °C. Above 600 °C, water molecules are lost and the opal surface and internal silanol molecules are completely dehydrated by heat effect, and the medium-temperature range structure of opal may begin to thermally reconstruct to six-membered rings of SiO₄ tetrahedra. Above 1,000 °C, the opal structure almost approaches that of silica glass with an average structure of six-membered rings. Above 1,200 °C, the opal changes to low-cristobalite; however, minor evidence of low-tridymite stacking was evident after heat treatment at 1,400 °C.