Magma (géologie) | EPFL Graph Search

thumb|Lave basaltique à Hawaï, constituée d'un magma basique. Un magma est une roche entièrement ou partiellement fondue. Il comporte nécessairement une phase liquide, généralement composée de silicates et contenant des gaz dissous. Il comporte souvent aussi, en suspension dans le liquide, une phase gazeuse (des bulles) et une ou plusieurs phases solides (des cristaux), qui proviennent respectivement de l'exsolution partielle des gaz dissous et de la solidification partielle du liquide par décompression et refroidissement. Le magma peut aussi comporter des éléments solides provenant des roches à travers lesquelles le magma est remonté : fragments de roches mantelliques ou crustales (xénolithes) et/ou cristaux isolés (xénocristaux). Les magmas se forment à haute température et sous haute pression par fusion partielle de la croûte terrestre ou du manteau. Moins denses que les roches solides de la lithosphère, ils sont entraînés vers le haut par la poussée d'Archimède, sous forme de dy

Distribution of platinum-group elements and Os isotopes in chromite ores from Mayari-Baracoa Ophiolitic Belt (eastern Cuba)

Reto Frei, Anders Meibom

The Mayari-Baracoa ophiolitic belt in eastern Cuba hosts abundant chromite deposits of historical economic importance. Among these deposits, the chemistry of chromite ore is very variable, ranging from high Al (Cr#=0.43-0.55) to high Cr (Cr#=0.60-0.83) compositions. Platinum-group element (PGE) contents are also variable (from 33 ppb to 1.88 ppm) and correlate positively with the Cr# of the ore. Bulk PGE abundances correlate negatively with the Pd/Ir ratio showing that chromite concentrates mainly Os, Ir and Ru which gives rise to the characteristic negatively sloped, chrondrite-normalized PGE patterns in many chromitites. This is consistent with the mineralogy of PGEs, which is dominated by members of the laurite-erlichmanite solid solution series (RuS2-OsS2), with minor amounts of irarsite (IrAsS), Os-Ir alloys, Ru-Os-Ir-Fe-Ni alloys, Ni-Rh-As, and sulfides of Ir, Os, Rh, Cu, Ni, and/or Pd. Measured Os-187/Os-188 ratios (from 0.1304 to 0.1230) are among the lower values reported for podiform chromitites. The Os-187/Os-188 ratios decrease with increasing whole-rock PGE contents and Cr# of chromite. Furthermore, gamma Os values of all but one of the chromitite samples are negative indicating a subchondiritc mantle source. gamma Os decrease with increasing bulk Os content and decreasing Re-187/Os-188 ratios. These mineralogical and geochemical features are interpreted in terms of chromite crystallization from melts varying in composition from back-arc basalts (Al-rich chromite) to boninites (Cr-rich chromite) in a suprasubduction zone setting. Chromite crystallization occurs as a consequence of magma mixing and assimilation of preexisting gabbro sills at the mantle-crust transition zone. Cr#, PGE abundances, and bulk Os isotopic composition of chromitites are determined by the combined effects of mantle source heterogeneity, the degree of partial melting, the extent of melt-rock interactions, and the local sulfur fugacity. Small-scale (mu m to cm) chemical and isotopic heterogeneities in the platinum-group minerals are controlled by the mechanism(s) of chromite crystallization in a heterogeneous environment created by the turbulent regime generated by successive inputs of different batches of melt.

2005

The statistical upper mantle assemblage

Anders Meibom

A fundamental challenge in modern mantle geochemistry is to link geochemical data with geological and geophysical observations. Most of the early geochemical models involved a layered mantle and the concept of geochemical reservoirs. Indeed, the two layer mantle model has been implicit in almost all geochemical literature and the provenance of oceanic island basalt (0113) and mid-ocean ridge basalt (MORB) [van Keken et al., Annu. Rev. Earth Planet. Sci. 30 (2002) 493-525]. Large-scale regions in the mantle, such as the 'convective' (i.e. well-stirred, homogeneous) upper mantle, sub-continental lithosphere, and the lower mantle were treated as distinct and accessible geochemical reservoirs. Here we discuss evidence for a ubiquitous distribution of small- to moderate-scale (i.e. 10(2)-10(5) m) heterogeneity in the upper mantle, which we refer to as the statistical upper mantle assemblage (SUMA). This heterogeneity forms as the result of long-term plate tectonic recycling of sedimentary and crustal components. The SUMA model does not require a convectively homogenized MORB mantle reservoir, which has become a frequently used concept in geochemistry. Recently, Kellogg et al. [Earth Planet. Sci. Lett. 204 (2002) 183-202] modeled MORB and OIB Sr and Nd isotopic compositions as local mantle averages of random distributions of depleted residues and recycled continental crustal material. In this model, homogenization of the MORB source region is achieved by convective stirring and mixing. In contrast, in the SUMA model, the isotopic compositions of MORB and OIB are the outcome of homogenization during sampling, by partial melting and magma mixing (e.g. [Helffrich and Wood, Nature 412 (2001) 501-507]), of a distribution of small- to moderate-scale upper mantle heterogeneity, as predicted by the central limit theorem. Thus, the 'SUMA' acronym also captures what we consider the primary homogenization process: sampling upon melting and averaging. SUMA does not require the participation of distinct (e.g. lower mantle) reservoirs to explain OIB compositions. The complementary methods outlined in this work and in e.g. Kellogg et al. and Helffrich and Wood, provide a strong link between geochemical data and potential geophysical observables, such as the degree of partial melting, size of the melting regime, the characteristic length scales of the chemical heterogeneity and bathymetry, seismic scattering and anisotropy. We support the view that statistical distributions of lithologic components and sampling theory should replace the concept of distinct, isolated geochemical reservoirs, and extensive convective stirring prior to sampling. (C) 2003 Elsevier B.V. All rights reserved.

2004

Unique large diamonds in a ureilite from Almahata Sitta 2008 TC3 asteroid

Philippe Gillet

The Almahata Sitta MS-170 ureilite (a piece of a breccia originating from the asteroid, 2008 TC3) consists mainly of olivine, with many diamond and graphite grains existing between the olivine grains. The occurrences of the diamonds are unique; i.e., (i) some diamonds exhibit sub-euhedral habits and (ii) some diamonds have large grain-size (up to about 40 mu m). Several diamonds are segmented into many fragments by fractures. Individual fragments have similar crystallographic orientation, which implies that the adjacent diamond segments were originally a single crystal. Large diamond assemblages occur besides such individual diamond grains. In one of the largest assemblages (almost about 100 mu m in size) has also the same crystallographic orientation. They can be regarded as the pieces of a previously unique single diamond, which provides evidence for large single-crystals diamond in meteorites. Almahata Sitta MS-170 is a meteorite fragment from the 2008 TC3 asteroid that underwent less shock than other ureilitic meteorites. It is unlikely that such large diamonds were formed from graphite through a shock-induced phase transformation during planetesimal collision, despite this idea being now widely accepted as the diamond formation mechanism of ureilites. Fine-scale heterogeneous distribution of impurities (hydrogen, nitrogen, and oxygen) exists in single crystal diamonds, indicative of sluggish growth. This distribution is reminiscent of sector zoning growth. Its grain size, the shock features of MS-170, and the C- and N-isotopic composition signatures allow us to revive classical and but not widely accepted models for diamond formation in ureilites; i.e., a diamond formed from partially melted magma or a C-O-H fluid in the deep interior of the ureilite parent-body or, alternatively, through a chemical vapor deposition (CVD) process in the solar nebula. Considering present mineralogical and isotopic features, the former scenario is more favorable. (C) 2015 Elsevier Ltd. All rights reserved.

Pergamon-Elsevier Science Ltd2015