Os-Hf-Sr-Nd isotopes and PGE were determined in peridotite xenoliths carried to the surface by Quaternary alkali basaltic magmas in the Tokinsky Stanovik Range on the Aldan shield. These data constrain the timing and nature of partial melting and metasomatism in the lithospheric mantle beneath SE Siberian craton. The xenoliths range from the rare fertile spinel lherzolites to the more abundant, strongly metasomatised olivine-rich (70-84%) rocks. Hf-Sr-Nd isotope compositions of the xenoliths are mainly within the fields of oceanic basalts. Most metasomatised xenoliths have lower Nd-143/Nd-144 and Hf-116/Hf-177 and higher Sr-117/Sr-86 than the host basalts indicating that the metasomatism is older and has distinct sources. A few xenoliths have elevated Hf-176/Hf-177 (up to 0.2838) and plot above the Hf-Nd mantle array defined by oceanic basalts.

An extensive study of peridotitic sulfide inclusion bearing diamonds and their prospective harzburgitic host rocks from the 53 Ma Panda kimberlite pipe, Ekati Mine, NWT Canada, has been undertaken with the Re-Os system to establish their age and petrogenesis. Diamonds with peridotitic sulfide inclusions have poorly aggregated nitrogen (< 30% N as B centers) at N contents of 200-800 ppm which differs from that of chromite and silicate bearing diamonds and indicates residence in the cooler portion of the Slave craton lithospheric mantle. For most of the sulfide inclusions, relatively low Re contents (average 0.457 ppm) and high Os contents (average 339 ppm) lead to extremely low Os-187/Os-188, typically << 0.05. An age of 3.52 +/- 0.17 Ga (MSWD = 0.46) and a precise initial Os-187/Os-188 of 0.1093 +/- 0.0001 are given by a single regression of 11 inclusions from five diamonds that individually provide coincident internal isochrons. This initial Os isotopic composition is 6% enriched in Os-187 over 3.5 Ga chondritic or primitive mantle. Sulfide inclusions with less radiogenic initial Os isotopic compositions reflect isotopic heterogeneity in diamond forming fluids. The harzburgites have even lower initial Os-187/Os-188 than the sulfide inclusions, some approaching the isotopic composition of 3.5 Ga chondritic mantle. In several cases isotopically distinct sulfides occur in different growth zones of the same diamond. This supports a model where C-O-H-S fluids carrying a radiogenic Os signature were introduced into depleted harzburgite and produced diamonds containing sulfides conforming to the 3.5 Ga isochron. Reaction of this fluid with harzburgite led to diamonds with less radiogenic inclusions while elevating the Os isotope ratios of some harzburgites. Subduction is a viable way of introducing such fluids. This implies a role for subduction in creating early continental nuclei at 3.5 Ga and generating peridotitic diamonds.

New volatile (H2O, CO2, S), halogen (F, Cl) and trace-element data for selected fresh MORB glasses are reported from two geologically and geophysically well-studied regions on the East Pacific Rise (8-10 degrees N and 12-14 degrees N) with distinct differences in spreading rate and magma supply. Sample locations include on-axis and young off-axis eruptions, as well as off-axis fissures, abyssal hills and pillow mounds. H2O, F, S and trace-element concentrations increase with decreasing MgO content, displaying over-enriched liquid lines of descent consistent with combined fractional and in-situ crystallization. A negative correlation between CO2/Nb and MgO indicates simultaneous degassing and magma crystallization, while broadening of this correlation to lower CO2/ Nb at constant MgO indicates shallow degassing and CO2 loss during magma transport to the seafloor.

In order to constrain the highly siderophile elements (HSE: Re and platinum group elements (PGE: Os, Ir, Ru, Pt and Pd)) host mineral(s) in refractory, base metal sulfide-free mantle residues, four very depleted spinel-harzburgites from the Lherz massif (France) have been analyzed for HSE in whole-rock and in major mineral separates (olivine, orthopyroxene, clinopyroxene and spinel) by isotope dilution. In addition, HSE host minerals have been separated and analyzed with a scanning electron microscope. Olivine and spinel show the highest HSE concentration especially for Os, Ir, Ru and Pt (up to 10 ppb) among the modally-major minerals, while the pyroxenes are 1-2 orders of magnitude poorer in HSE. The major minerals account for less than 30% of the whole-rock platinum group element budget. On the other hand, rare, micron to sub-micron platinum group minerals (PGM), such as Ru-Os +/- Ir sulfides and Pt-Ir +/- Os alloys, likely located in the intergranular spaces of the refractory depleted harzburgite, account for 50-100% of the HSE budget. The PGM grains are interpreted to be residual, having formed in response to the complete consumption of the base-metal sulfides by the high degree of partial melting (i.e. 23-24%) experienced by these samples. As they sequester the compatible platinum group elements (Os, Ir, Ru and Pt) in the mantle residue, these PGM provide key constraints for the modelling of PGE contents in terrestrial basalts (e.g. the solid/liquid partition coefficients needed to account for the compatible behavior of these elements in the mantle residue) and for understanding the long-lived Os isotope heterogeneities of the upper mantle, especially the old Re-Os ages found in young oceanic mantle. In fact, because of their Os-rich compositions and high melting temperatures, these microphases are likely to preserve their initial Os isotopic compositions unmodified over multiple events of mantle melting and mixing, and therefore generate, through recycling, heterogeneous Os isotopic signatures at different scales in the convecting mantle. (C) 2007 Elsevier Ltd. All rights reserved.

We have precisely measured Os isotopic ratios in bulk samples of five carbonaceous, two enstatite and two ordinary chondrites, as well as the acid-resistant residues of three carbonaceous chondrites. All bulk meteorite samples have uniform Os-186/Os-188, Os-188/Os-189 and Os-190/Os-189 ratios, when decomposed by an alkaline fusion total digestion technique. These ratios are also identical to estimates for Os in the bulk silicate Earth. Despite Os isotopic homogeneity at the bulk meteorite scale, acid insoluble residues of three carbonaceous chondrites are enriched in Os-186, Os-188 and Os-190, isotopes with major contributions from stellar s-process nucleosynthesis. Conversely, these isotopes are depleted in acid soluble portions of the same meteorites. The complementary enriched and depleted fractions indicate the presence of at least two types of Os-rich components in these meteorites, one enriched in Os isotopes produced by s-process nucleosynthesis, the other enriched in isotopes produced by the r-process. Presolar silicon carbide is the most probable host for the s-process-enriched Os present in the acid insoluble residues. Because the enriched and depleted components present in these meteorites are combined in proportions resulting in a uniform chondritic/terrestrial composition, it requires that disparate components were thoroughly mixed within the solar nebula at the time of the initiation of planetesimal accretion. This conclusion contrasts with evidence from the isotopic compositions of some other elements (e.g., Sm, Nd, Ru, Mo) that suggests heterogeneous distribution of matter with disparate nucleosynthetic sources within the nebula. Published by Elsevier B.V.