西南日本の熱変成超苦鉄質岩体中のかんらん石と輝石の組成変化に関する覚書

This short article presents some diagrams showing the compositional variations of primary and metamorphic olivine, orthopyroxene and clinopyroxene in peridotites and serpentinites from thermally metamorphosed ultramafic complexes in SW Japan. In contrast to olivine, which shows a gradual change of chemical composition corresponding with metamorphic grade, orthopyroxene and clinopyroxene show clear differences in composition between primary and metamorphic phases. Compared with primary pyroxenes, even though their compositions could be variable depending on original rock composition, metamorphic orthopyroxene and metamorphic clinopyroxene is clearly deficient in Cr(2)O(3) and CaO, and in Cr(2)O(3) and Al(2)O(3), respectively. These characteristics are useful for the discrimination between the pyroxenes of different origin

Mafic alkaline metasomatism in the lithosphere underneath East Serbia: evidence from the study of xenoliths and the host alkali basalts

Effects of mafic alkaline metasomatism have been investigated by a combined study of the East Serbian mantle xenoliths and their host alkaline rocks. Fertile xenoliths and tiny mineral assemblages found in depleted xenoliths have been investigated. Fertile lithologies are represented by clinopyroxene (cpx)-rich lherzolite and spinel (sp)-rich olivine websterite containing Ti–Al-rich Cr-augite, Fe-rich olivine, Fe–Al-rich orthopyroxene and Al-rich spinel. Depleted xenoliths, which are the predominant lithology in the suite of East Serbian xenoliths, are harzburgite, cpx-poor lherzolite and rare Mg-rich dunite. They contain small-scale assemblages occurring as pocket-like, symplectitic or irregular, deformation-assisted accumulations of metasomatic phases, generally composed of Ti–Al- and incompatible element-rich Cr-diopside, Cr–Fe–Ti-rich spinel, altered glass, olivine, apatite, ilmenite, carbonate, feldspar, and a high-TiO2 (c. 11 wt%) phlogopite. The fertile xenoliths are too rich in Al, Ca and Fe to simply represent undepleted mantle. By contrast, their composition can be reproduced by the addition of 5–20 wt% of a basanitic melt to refractory mantle. However, textural relationships found in tiny mineral assemblages inside depleted xenoliths imply the following reaction: opx+sp1 (primary mantle Cr-spinel) ±phlogopite+Si-poor alkaline melt=Ti–Al-cpx+sp2 (metasomatic Ti-rich spinel)±ol±other minor phases. Inversion modelling, performed on the least contaminated and most isotopically uniform host basanites (87Sr/86Sr=c. 0.7031; 143Nd/144Nd=c. 0.5129), implies a source that was enriched in highly and moderately incompatible elements (c. 35–40× chondrite for U–Th–Nb–Ta, 2× chondrite for heavy rare earth elements (HREE), made up of clinopyroxene, carbonate (c. 5%), and traces of ilmenite (c. 1%) and apatite (c. 0.05%). A schematic model involves: first, percolation of CO2- and H2O-rich fluids and precipitation of metasomatic hydrous minerals; and, second, the subsequent breakdown of these hydrous minerals due to the further uplift of hot asthenospheric mantle. This model links intraplate alkaline magmatism to lithospheric mantle sources enriched by sublithospheric melts at some time in the past

The formation of boundary clinopyroxenes and associated glass veins in type B1 CAIs

We used focused ion beam thin section preparation and scanning transmission electron microscopy (FIB/STEM) to examine the interfacial region between spinel and host melilite for spinel grains in type B1 inclusions from the Allende and Leoville carbonaceous chondrites. Boundary clinopyroxenes decorating spinel surfaces have compositions similar to those of coarser clinopyroxenes from the same region of the inclusion, suggesting little movement after formation. Host melilite displays no anomalous compositions near the interface and late-stage minerals are not observed, suggesting that boundary pyroxenes did not form by crystallization of residual liquid. Allende spinels display either direct spinel-melilite contact or an intervening boundary clinopyroxene between the two phases. Spinel-melilite interfacial regions in a Leoville B1 are more complex, with boundary clinopyroxene, as observed in Allende, but also variable amounts of glass, secondary calcite, perovskite, and an Mg-, Al-, OH-rich and Ca-, Si-poor crystalline phase that may be a layered double hydrate. One possible scenario of formation for the glass veins is that open system alteration of melilite produced a porous, hydrated aggregate of Mg-carpholite or sudoite + aluminous diopside that was shock melted and quenched to a glass. The hydrated crystalline phase we observed may have been a shocked remnant of the precursor phase assemblage, but is more likely to have formed later by alteration of the glass. In the mantle, boundary clinopyroxenes may have been crystallized from Ti-rich liquids formed by the direct dissolution of perovskite and an associated Sc-Zr-rich phase or as a reaction product between dissolving perovskite and liquid. In the core, any perovskite and associated Ti-enriched liquids that may have originally been present disappeared before the growth of boundary clinopyroxene, and the observed boundary clinopyroxene may have nucleated and grown from the liquid, along with the larger core clinopyroxene

Ultramafic xenoliths from the Bearpaw Mountains, Montana, USA: evidence for multiple metasomatic events in the lithospheric mantle beneath the Wyoming craton

Ultramafic xenoliths in Eocene minettes of the Bearpaw Mountains volcanic field (Montana, USA), derived from the lower lithosphere of the Wyoming craton, can be divided based on textural criteria into tectonite and cumulate groups. The tectonites consist of strongly depleted spinel lherzolites, harzburgites and dunites. Although their mineralogical compositions are generally similar to those of spinel peridotites in off-craton settings, some contain pyroxenes and spinels that have unusually low Al2O3 contents more akin to those found in cratonic spinel peridotites. Furthermore, the tectonite peridotites have whole-rock major element compositions that tend to be significantly more depleted than non-cratonic mantle spinel peridotites (high MgO, low CaO, Al2O3 and TiO2) and resemble those of cratonic mantle. These compositions could have been generated by up to 30% partial melting of an undepleted mantle source. Petrographic evidence suggests that the mantle beneath the Wyoming craton was re-enriched in three ways: (1) by silicate melts that formed mica websterite and clinopyroxenite veins; (2) by growth of phlogopite from K-rich hydrous fluids; (3) by interaction with aqueous fluids to form orthopyroxene porphyroblasts and orthopyroxenite veins. In contrast to their depleted major element compositions, the tectonite peridotites are mostly light rare earth element (LREE)-enriched and show enrichment in fluid-mobile elements such as Cs, Rb, U and Pb on mantle-normalized diagrams. Lack of enrichment in high field strength elements (HFSE; e.g. Nb, Ta, Zr and Hf) suggests that the tectonite peridotites have been metasomatized by a subduction-related fluid. Clinopyroxenes from the tectonite peridotites have distinct U-shaped REE patterns with strong LREE enrichment. They have 143Nd/144Nd values that range from 0·5121 (close to the host minette values) to 0·5107, similar to those of xenoliths from the nearby Highwood Mountains. Foliated mica websterites also have low 143Nd/144Nd values (0·5113) and extremely high 87Sr/86Sr ratios in their constituent phlogopite, indicating an ancient (probably mid-Proterozoic) enrichment. This enriched mantle lithosphere later contributed to the formation of the high-K Eocene host magmas. The cumulate group ranges from clinopyroxene-rich mica peridotites (including abundant mica wehrlites) to mica clinopyroxenites. Most contain >30% phlogopite. Their mineral compositions are similar to those of phenocrysts in the host minettes. Their whole-rock compositions are generally poorer in MgO but richer in incompatible trace elements than those of the tectonite peridotites. Whole-rock trace element patterns are enriched in large ion lithophile elements (LILE; Rb, Cs, U and Pb) and depleted in HFSE (Nb, Ta Zr and Hf) as in the host minettes, and their Sr–Nd isotopic compositions are also identical to those of the minettes. Their clinopyroxenes are LREE-enriched and formed in equilibrium with a LREE-enriched melt closely resembling the minettes. The cumulates therefore represent a much younger magmatic event, related to crystallization at mantle depths of minette magmas in Eocene times, that caused further metasomatic enrichment of the lithosphere

Trace element geochemistry of peridotites from the Izu-Bonin-Mariana Forearc, Leg 125

Trace element analyses (first-series transition elements, Ti, Rb, Sr, Zr, Y, Nb, and REE) were carried out on whole rocks and minerals from 10 peridotite samples from both Conical Seamount in the Mariana forearc and Torishima Forearc Seamount in the Izu-Bonin forearc using a combination of XRF, ID-MS, ICP-MS, and ion microprobe. The concentrations of incompatible trace elements are generally low, reflecting the highly residual nature of the peridotites and their low clinopyroxene content (n ratios in the range of 0.05-0.25; several samples show possible small positive Eu anomalies. LREE enrichment is common to both seamounts, although the peridotites from Conical Seamount have higher (La/Ce)n ratios on extended chondrite-normalized plots, in which both REEs and other trace elements are organized according to their incompatibility with respect to a harzburgitic mantle. Comparison with abyssal peridotite patterns suggests that the LREEs, Rb, Nb, Sr, Sm, and Eu are all enriched in the Leg 125 peridotites, but Ti and the HREEs exhibit no obvious enrichment. The peridotites also give positive anomalies for Zr and Sr relative to their neighboring REEs. Covariation diagrams based on clinopyroxene data show that Ti and the HREEs plot on an extension of an abyssal peridotite trend to more residual compositions. However, the LREEs, Rb, Sr, Sm, and Eu are displaced off this trend toward higher values, suggesting that these elements were introduced during an enrichment event. The axis of dispersion on these plots further suggests that enrichment took place during or after melting and thus was not a characteristic of the lithosphere before subduction. Compared with boninites sampled from the Izu-Bonin-Mariana forearc, the peridotites are significantly more enriched in LREEs. Modeling of the melting process indicates that if they represent the most depleted residues of the melting events that generated forearc boninites they must have experienced subsolidus enrichment in these elements, as well as in Rb, Sr, Zr, Nb, Sm, and Eu. The lack of any correlation with the degree of serpentinization suggests that low-temperature fluids were not the prime cause of enrichment. The enrichment in the high-field-strength elements also suggests that at least some of this enrichment may have involved melts rather than aqueous fluids. Moreover, the presence of the hydrous minerals magnesio-hornblende and tremolite and the common resorption of orthopyroxene indicate that this high-temperature peridotite-fluid interaction may have taken place in a water-rich environment in the forearc following the melting event that produced the boninites. The peridotites from Leg 125 may therefore contain a record of an important flux of elements into the mantle wedge during the initial formation of forearc lithosphere. Ophiolitic peridotites with these characteristics have not yet been reported, perhaps because the precise equivalents to the serpentinite seamounts have not been analyzed

Impulsive supply of volatile-rich magmas in the shallow plumbing system of Mt. Etna volcano

Magma dynamics at Mt. Etna volcano are frequently recognized as the result of complex crystallization regimes that, at shallow crustal levels, unexpectedly change from H2O -undersaturated to H2O-saturated conditions, due to the impulsive and irregular arrival of volatile-rich magmas from mantle depths. On this basis, we have performed hydrous crystallization experiments for a quantitative understanding of the role of H2O in the differentiation of deep-seated trachybasaltic magmas at the key pressure of the Moho transition zone. For H2O = 2.1–3.2 wt %, the original trachybasaltic composition shifts towards phonotephritic magmas never erupted during the entire volcanic activity of Mt. Etna. Conversely, for H2O = 3.8–8.2 wt %, the obtained trachybasalts and basaltic trachyandesites reproduce most of the pre-historic and historic eruptions. The comparison with previous low pressure experimental data and natural compositions from Mt. Etna provides explanation for (1) the abundant release of H2O throughout the plumbing system of the volcano during impulsive ascent of deep-seated magmas; (2) the upward acceleration of magmas feeding gas-dominated, sustained explosive eruptions; (3) the physicochemical changes of gas-fluxed magmas ponding at shallow crustal levels; and (4) the huge gas emissions measured at the summit craters and flank vents which result in a persistent volcanic gas plume

Abundance and Partitioning of OH in a High-pressure Magmatic System: Megacrysts from the Monastery Kimberlite, South Africa

Concentrations of OH, and major and trace elements were determined in a suite of mantle-derived megacrysts that represent the crystallization products of a kimberlite-like magma at ~5 GPa and ~1400–1100°C. OH concentrations, determined by single-crystal Fourier transform infrared spectroscopy, display the following ranges (ppmw H2O): olivine 54–262, orthopyroxene 215–263, garnet 15–74, clinopyroxene 195–620, and zircon 28–34. High OH concentrations in olivine imply mantle conditions of origin, with limited H loss during ascent. OH is consistently correlated with megacryst composition, exhibiting trends with Mg-number that are similar to those of other minor and trace elements and indicating a record of high-pressure magmatic evolution. H substitution is not coupled to minor elements in olivine, but may be in ortho- and clinopyroxene. The OH–Mg-number trends of garnet and clinopyroxene show inflections related to co-precipitation of ilmenite, suggesting minor element (Ti) influence on OH partitioning. During differentiation, relative OH enrichment in clinopyroxene and olivine is consistent with proportional dependence on water activity, whereas that in garnet suggests a higher power-law dependence and/or influence of temperature. Inter-mineral distribution coefficients for OH between cpx, opx, olivine and zircon are thus constant, whereas partitioning between these minerals and garnet shows a factor 4–10 variation, correlated regularly with composition (and temperature). Calculation of solid–melt partition coefficients for H at 5 GPa over a range of magmatic evolution from 1380 to 1250°C yields: ol 0·0053–0·0046, opx 0·0093–0·0059, cpx 0·016–0·013, gt 0·0014–0·0003, bulk (garnet lherzolite–melt) 0·0063–0·0051. These are consistent with experimental studies and similar to values inferred from mid-ocean ridge basalt geochemistry, confirming the moderate incompatibility of H in mantle melting

Mineral chemistry of late Variscan gabbros from central Spain: constraints on crystallisation processes and nature of the parental magmas

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Staged storage and magma convection at Ambrym Volcano, Vanuatu

New mineral-melt thermobarometry and mineral chemistry data are presented for basaltic scoriae erupted from the Mbwelesu crater of Ambrym volcano, Vanuatu, during persistent lava lake activity in 2005 and 2007. These data reveal crystallisation conditions and enable the first detailed attempt at reconstruction of the central magma plumbing system of Ambrym volcano. Pressures and temperatures of magma crystallisation at Ambrym are poorly constrained. This study focuses on characterising the magma conditions underlying the quasipermanent lava lakes at the basaltic central vents, and examines petrological evidence for magma circulation. Mineral-melt equilibria for clinopyroxene, olivine and plagioclase allow estimation of pressures and temperatures of crystallisation, and reveal two major regions of crystallisation, at 24–29 km and 11–18 km depth, in agreement with indications from earthquake data of crustal storage levels at c.25–29 km and 12–21 km depth. Temperature estimates are ~1150–1170 ºC for the deeper region, and ~1110 1140 ºC in the midcrustal region, with lower temperatures of ~1090–1100 ºC for late-stage crystallisation. More primitive plagioclase antecrysts are thought to sample a slightly more mafic melt at sub-Moho depths. Resorption textures combined with effectively constant mafic mineral compositions suggest phenocryst convection in a storage region of consistent magma composition. In addition, basalt erupted at Ambrym has predominantly maintained a constant composition throughout the volcanic succession. This, coupled with recurrent periods of elevated central vent activity on the scale of months, suggest frequent magmatic recharge via steady-state melt generation at Ambrym