Crustal structure in the Mizuho Plateau, East Antarctica, by a two-dimensional ray approximation

Studies on the crustal and upper-mantle structure in Antarctica have been one of the major contributions to Antarctic research since the International Geophysical Year of 1957–1958. Many refraction surveys with small charge size have been conducted in Antarctica, but long-range experiments were also made in 5 regions on the margin of the Antarctic continent.In 1979–1981, the scientific program of the Japanese Antarctic Research Expedition was focused on the earth sciences, and in particular, an explosion seismic experiment along a long survey line was the major item during these years. An experiment along a 300 km-long line with three shots and 27 observation stations was successfully made in the northern Mizuho Plateau, East Antarctica.From the analysis of travel times and the amplitude study of synthetic seismograms, the crustal structure of the northern Mizuho Plateau was determined. The depths of the Conrad and the Moho discontinuties were determined as 31 km and 42 km, respectively. The P-wave velocity and depth relation was determined as 6.0 km/s on the surface of the bedrock, 6.3 km/s at a depth of 2 km, 6.8 km/s at the Conrad and 7.9 km/s at the Moho. The velocity in the crust increases gradually. The crustal structure obtained is representative of East Antarctica.     

Petrology of peridotite xenoliths in lamprophyre from Shingu,Southwestern Japan: Implications for origin of Fe-rich mantle peridotites

Summary Xenoliths of harzburgite, lherzolite, dunite and wehrlite (= Group I rocks) in lamprophyre dikes from Shingu are accompanied by large amounts of ultramafic-mafic xeno liths with Al- and Ti-rich clinopyroxene and/or kaersuite (websterite, clinopyroxenite, kaersutite rock, gabbro and anorthosite) (= Group II rocks). The latter rocks often crosscut the Group I rocks as veinlets, indicating that Group II rocks are younger. Although harzburgites and lherzolite from Shingu have ordinary modal compositions, the constituent minerals have extraordinary chemical characteristics; low Mg and Cr and high Ti, Al and Fe³⁺. Fo values of olivine range from 91 to 77. Cr/(Cr + Al) atomic ratios of spinel are lower than 0.5 even in harzburgites. Fe³⁺/(Cr+Al+Fe³⁺) atomic ratios of spinel are sometimes over 0.1. TiO₂ contents of clinopyroxene often exceed 0.5 wt%. These characteristics are revealed when Group I rocks are veined or selvaged by Group 11 rocks; chemical compositions of minerals in peridotites systematically change forwards the latter. This strongly suggests that injections of melts with alkali basaltic affinity which had precipitated Group 11 rocks resulted in diffusion metasomatism on the Group I rocks.It is likely that the metasomatized peridotites are widespread underneath the areas where alkali basalt magmatism had fluorished, such as southwestern Japan. Some of Fe-rich lherzolite and harzburgite xenoliths reported in the literature are possibly metasomatites.

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Petrologie von Peridotit-Xenolithen in Lamprophyren von Shingu, Südwest-Japan: Hinweise auf die Herkunft Fe-reicher Mantel-Peridotite

Zusammenfassung In lamprophyrischen Gängen von Shingu kommen Xenolithe von Harzburgit, Lherzolith, Dunit and Wehrlit (= Gesteinsgruppe I) vor. Sie werden von einer Vielzahl von ultramaf-isch-mafischen Xenolithen mit Al- and Ti-reichem Klinopyroxen and/oder Kaersutit (Websterit, Klinopyroxenit, Kaersutit-Gestein, Gabbro and Anorthosit) (=Gesteinsgruppe II) begleitet, die die Xenolithe der Gruppe I häufig gangförmig durchkreuzen, was auf ein jü ngeres Alter der Gesteinsgruppe II hinweist. Obwohl die Harzburgite and Lherzolithe von Shingu übliche modale Mineralbestände aufweisen, sind die Mineralchemismen außergewöhnlich: Niedrige Mg- and Cr- and hohe Ti-, Al- and Fe³⁺-Gehalte. Die Fo-Gehalte von Olivin reichen von 91 bis 77. Die Cr/(Cr+Al)-Atom-Verhältnisse der Spinelle sind kleiner als 0,5, sogar in den Harzburgiten; die Fe³⁺/(Cr+Al+Fe³⁺)-Atom-Verhaltnisse teilweise größer als 0,1. Der TiO₂-Gehalt im Klinopyroxen ist meist über 0,5 Gew.%. Diese Charakteristika zeigen sich dort, wo die Gesteinsgruppe II die Gesteinsgruppe I durchschlägt oder kontaktiert. Der Mineralchemismus in den Peridotiten ändert sich dabei systematisch. Es wird vermutet, daß Schmelzinjektionen mit alkali-basaltischer Affinität, von denen die Gesteinsgruppe II herstammt, eine Diffusions-Metasomatose der Gesteinsgruppe I verursacht hat.Es wird angenommen, daß metasomatisierte Peridotite an der Basis von alkali-basaltischem Magmatismus weft verbreitet sind, wie zum Beispiel in Südwest-Japan. Einige in der Literatur aufscheinende Fe-reiche Lherzolith- and Harzburgit-Xenolithe sind möglicherweise metasomatisch entstanden.

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With 6 Figures     

Multiple parent bodies of ordinary chondrites

Thermal histories of chondrite parent bodies are calculated from an initial state with material in a powder-like form, taking into account the effect of consolidation state on thermal conductivity. The very low thermal conductivity of the starting materials makes it possible for a small body with a radius of less than 100 km to be heated by several hundred degrees even if long-lived radioactive elements in chondritic abundances are the only source of heat. The maximum temperature is determined primarily by the temperature at which sintering of the constituent materials occurs. The thermal state of the interior of a chondrite parent body after sintering has begun is nearly isothermal. Near the surface, however, where the material is unconsolidated and the thermal conductivity is much lower, the thermal gradient is quite large. This result contradicts the conventional “onion-shell” model of chondrite parent bodies. But because the internal temperature is almost constant through the whole body, it supports a “multiple-parent bodies” model, according to which each petrologic type of chondrite comes from a different parent body.     

Formation of a solid solution in the MgSiO3–MnSiO3 perovskite system

Experiments using laser-heated diamond anvil cells combined with synchrotron X-ray diffraction and SEM–EDS chemical analyses have confirmed the existence of a complete solid solution in the MgSiO₃–MnSiO₃ perovskite system at high pressure and high temperature. The (Mg, Mn)SiO₃ perovskite produced is orthorhombic, and a linear relationship between the unit cell parameters of this perovskite and the proportion of MnSiO₃ components incorporated seems to obey Vegard’s rule at about 50 GPa. The orthorhombic distortion, judged from the axial ratios of a/b and \( \sqrt{2}\,a/c, \) monotonically decreases from MgSiO₃ to MnSiO₃ perovskite at about 50 GPa. The orthorhombic distortion in (Mg_0.5, Mn_0.5)SiO₃ perovskite is almost unchanged with increasing pressure from 30 to 50 GPa. On the other hand, that distortion in (Mg_0.9, Mn_0.1)SiO₃ perovskite increases with pressure. (Mg, Mn)SiO₃ perovskite incorporating less than 10 mol% of MnSiO₃ component is quenchable. A value of the bulk modulus of 256(2) GPa with a fixed first pressure derivative of four is obtained for (Mg_0.9, Mn_0.1)SiO₃. MnSiO₃ is the first chemical component confirmed to form a complete solid solution with MgSiO₃ perovskite at the P–T conditions present in the lower mantle.