Internal distribution of Li and B in serpentinites from the Feather River Ophiolite, California based on laser ablation ICP-MS

International audienceLaser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) analyses of B and Li in serpentinized peridotites from the Feather River Ophiolite (California) indicates that B is enriched in serpentine minerals compared to the whole-rock and less altered olivine grains while Li in serpentine is depleted or comparable to whole-rock Li. The high B contents of serpentine minerals correlate with the relatively enriched whole-rock B contents. The low Li contents of serpentine minerals are consistent with the relatively low Li whole-rock contents and suggest that only small amounts of Li were added during serpentinization or that some Li was even leached out. A simple model of partial melting shows that Li/Yb increases with increasing melt depletion (and clinopyroxene depletion) in the peridotitic residue because Li is most compatible in olivine while Yb is most compatible in clinopyroxene. Thus, high Li/Yb ratios in peridotites by themselves do not indicate secondary enrichments in Li. However, Li/Yb and Yb contents of many of the Feather River Ophiolites plot above the melt depletion curve in Li/Yb versus Yb space, indicating that these serpentinites experienced subtle and preferential enrichments in Li during serpentinization. If serpentinized oceanic lithospheric mantle, as represented by the Feather River Ophiolite, is important in subduction recycling, then recycled mantle domains having a serpentinite protolith might be characterized by strong B enrichments but only small Li enrichments

Pt, Au, Pd and Ru Partitioning Between Mineral and Silicate Melts: The Role of Metal Nanonuggets

The partition coefficients of Pt and other Pt Group Elements (PGE) between metal and silicate D(sub Metal-Silicate) and also between silicate minerals and silicate melts D(sub Metal-Silicate) are among the most challenging coefficients to obtain precisely. The PGE are highly siderophile elements (HSE) with D(sub Metal-Silicate) >10(exp 3) due to the fact that their concentrations in silicates are very low (ppb to ppt range). Therefore, the analytical difficulty is increased by the possible presence of HSE-rich-nuggets in reduced silicate melts during experiments). These tiny HSE nuggets complicate the interpretation of measured HSE concentrations. If the HSE micro-nuggets are just sample artifacts, then their contributions should be removed before calculations of the final concentration. On the other hand, if they are produced during the quench, then they should be included in the analysis. We still don't understand the mechanism of nugget formation well. Are they formed during the quench by precipitation from precursor species dissolved homogeneously in the melts, or are they precipitated in situ at high temperature due to oversaturation? As these elements are important tracers of early planetary processes such as core formation, it is important to take up this analytical and experimental challenge. In the case of the Earth for example, chondritic relative abundances of the HSE in some mantle xenoliths have led to the concept of the "late veneer" as a source of volatiles (such as water) and siderophiles in the silicate Earth. Silicate crystal/liquid fractionation is responsible for most, if not all, the HSE variation in the martian meteorite suites (SNC) and Pt is the element least affected by these fractionations. Therefore, in terms of reconstructing mantle HSE abundances for Mars, Pt becomes a very important player. In the present study, we have performed high temperature experiments under various redox conditions in order to determine the abundances of Pt, Au, Ru and Pd in minerals (olivine and diopside) and in silicate melts, but also to characterize the sizes, density and chemistry of HSE nuggets when present in the samples

A " high 4 He/ 3 He " mantle material detected under the East Pacific Rise (15°4′N)

International audienceWe investigate in details helium isotope data reported in Mougel et al. (2014) for 14 basaltic samples collected on the East Pacific Rise by submersible (15°4′N) where the ridge interacts with the Mathematician seamounts. Samples locations are separated by only few hundred meters across a 15 km along-axis profile. The data reveal a strong geochemical variability that has never been observed at such high spatial resolution for helium isotope compositions. Moreover, they reveal an unusually high 4 He/ 3 He mantle component also characterized by unradiogenic lead, atypical in oceanic basalts. He-Pb systematics suggests a mixture between a nonradiogenic lead and radiogenic helium pyroxenitic component, recycled from the deep continental lithosphere and the ambient peridotitic mantle. The He isotope difference between these two end-members can be interpreted as a time evolution of two distinct mantle sources after a slight (U + Th)/ 3 He fractionation, likely due to some ancient degassing during the formation of deep continental pyroxenites

Trace element geochemistry of K-rich impact spherules from howardites

The howardite-eucrite-diogenite (HED) achondrites are a group of meteorites that probably originate from the asteroid Vesta. Howardites are complex polymict breccias that sometimes contain, in addition to various rock debris, impact melt glasses which show an impressive range of compositions. In this paper we report on the geochemistry and O isotopes of a series of 6 Saharan polymict breccias (4 howardites and 2 polymict eucrites), and on the trace element abundances of high-K impact spherules found in two of them, Northwest Africa (NWA) 1664 and 1769, which are likely paired. The high-K impact spherules found in the howardites NWA 1664 and NWA 1769 display remarkable trace element patterns. Compared to eucrites or howardites, they all show prominent enrichments in Cs, Rb, K, Li and Ba, strong depletion in Na, while the REE and other refractory elements are unfractionated. These features could not have been generated during impact melting of their host howardites, nor other normal HED target materials. The involvement of Na-poor rocks, and possibly rocks of granitic composition, appears likely. Although these lithologies cannot be well constrained at present, our results demonstrate that the surface of Vesta is certainly more diverse than previously thought. Indeed, despite the large number of available HED meteorites (about 1000 different meteorites), the latter are probably not sufficient to describe the whole surface of their parent body

Genetic Relations Between the Aves Ridge and the Grenada Back-Arc Basin, East Caribbean Sea

The Grenada Basin separates the active Lesser Antilles Arc from the Aves Ridge, described as a Cretaceous‐Paleocene remnant of the “Great Arc of the Caribbean.” Although various tectonic models have been proposed for the opening of the Grenada Basin, the data on which they rely are insufficient to reach definitive conclusions. This study presents, a large set of deep‐penetrating multichannel seismic reflection data and dredge samples acquired during the GARANTI cruise in 2017. By combining them with published data including seismic reflection data, wide‐angle seismic data, well data and dredges, we refine the understanding of the basement structure, depositional history, tectonic deformation and vertical motions of the Grenada Basin and its margins as follows: (1) rifting occurred during the late Paleocene‐early Eocene in a NW‐SE direction and led to seafloor spreading during the middle Eocene; (2) this newly formed oceanic crust now extends across the eastern Grenada Basin between the latitude of Grenada and Martinique; (3) asymmetrical pre‐Miocene depocenters support the hypothesis that the southern Grenada Basin originally extended beneath the present‐day southern Lesser Antilles Arc and probably partly into the present‐day forearc before the late Oligocene‐Miocene rise of the Lesser Antilles Arc; and (4) the Aves Ridge has subsided along with the Grenada Basin since at least the middle Eocene, with a general subsidence slowdown or even an uplift during the late Oligocene, and a sharp acceleration on its southeastern flank during the late Miocene. Until this acceleration of subsidence, several bathymetric highs remained shallow enough to develop carbonate platforms

11B-rich fluids in subduction zones: the role of antigorite dehydration in subducting slabs and boron isotope heterogeneity in the mantle

Serpentinites form by hydration of mantle peridotite and constitute the largest potential reservoir of fluid-mobile elements entering subduction zones. Isotope ratios of one such element, boron, distinguish fluid contributions from crustal versus serpentinite sources. Despite 85% of boron hosted within abyssal peridotite being lost at the onset of subduction at the lizardite-to-antigorite transition, a sufficient cargo of boron to account for the composition of island arc magma is retained (c. 7 μg g− 1, with a δ11B of + 22‰) until the down-going slab reaches the antigorite-out isograd. At this point a 11B-rich fluid, capable of providing the distinctive δ11B signature of island arc basalts, is released. Beyond the uniquely preserved antigorite-out isograd in serpentinites from Cerro del Almirez, Betic Cordillera, Spain, the prograde lithologies (antigorite–chlorite–orthopyroxene–olivine serpentinite, granofels-texture chlorite-harzburgite and spinifex-texture chlorite-harzburgite) have very different boron isotope signatures (δ11B = − 3 to + 6‰), but with no significant difference in boron concentration compared to the antigorite-serpentinite on the low P–T side of the isograd. 11B-rich fluid, which at least partly equilibrated with pelagic sediments, is implicated in the composition of these prograde lithologies, which dehydrated under open-system conditions. Serpentinite-hosted boron lost during the early stages of dehydration is readily incorporated into forearc peridotite. This, in turn, may be dragged to sub-arc depths as a result of subduction erosion and incorporated in a mélange comprising forearc serpentinite, altered oceanic crust and pelagic sediment. At the antigorite-out isograd it dehydrates, thus potentially providing an additional source of 11B-rich fluids

Origin of Light Noble Gases (He, Ne, and Ar) on Earth: A Review

We review the different scenarios for the origin of light noble gases (He, Ne, and Ar) on Earth. Several sources could have contributed to the Earth's noble gas budget: implanted solar wind, solar nebula gas, chondrites, and comets. Although there is evidence for solar-like neon in the Earth's mantle, questions remain as to its origin. A new compilation of noble gas data in lunar soils, interplanetary dust particles, micrometeorites, and solar wind allows examination of the implanted solar wind composition, which is key to understanding the solar-like mantle neon isotope composition. We show that lunar soils that reflect this solar-wind-implanted signature have a Ne-20/Ne-22 ratio very close to that of ocean island basalts. New data and calculations illustrate that the measured plume source Ne-20/Ne-22 ratio is close to the primitive mantle ratio, when taking into account mixing with the upper mantle (that has lower Ne-20/Ne-22 ratio). This favors early solar wind implantation to account for the origin of light volatiles (He, Ne, and possibly H) in the Earth's mantle: they were incorporated by solar wind irradiation into the Earth's precursor grains during the first few Myr of the solar system's formation. These grains must have partially survived accretion processes (only a few percent are needed to satisfy the Earth's budget of light volatiles). As for the atmosphere, the neon isotope composition can be explained by mixing 36% of mantle gases having this solar-wind-implanted signature and 64% of chondritic gases delivered in a late veneer phase

Quantifying trace element disequilibria in mantle xenoliths and abyssal peridotites

We apply a tool based on element distribution between orthopyroxene and clinopyroxene for quantifying rare earth element (REE) disequilibria in ultramafic rocks in the subsolidus state. We present case studies of the REE contents of mineral cores in mantle xenoliths and abyssal peridotites using in situ analytical tools. Even when only mineral cores are measured (to avoid enriched rims), equilibrium is not always achieved on the mineral scale. Mineral cores in mantle xenoliths are closer to equilibrium than those in abyssal peridotites even though mantle xenoliths are known to be light REE-contaminated from the host lava. In the case of the abyssal peridotites, 13 out of 14 are out of equilibrium with the least metasomatized most in disequilibrium and the most metasomatized closest to equilibrium. We discuss hypotheses for these observations, but regardless of what caused the disequilibria, this tool allows one to “see through” the effects of secondary processes, such as infiltration by fluid inclusions via cracks and diffusive exchange between minerals and melts/fluids along grain boundaries. The ease of making in situ REE measurements makes this tool formidable in identifying different generations of clinopyroxenes in ultramafic lithologies. Such data will complement the interpretation of isotopic and petrographic studies of continental and oceanic lithospheric mantle

A highly unradiogenic lead isotopic signature revealed by volcanic rocks from the East Pacific Rise

International audienceRadiogenic isotopes in oceanic basalts provide a window into the different geochemical components defining the composition of Earth's mantle. Here we report the discovery of a novel geochemical signature in volcanic glasses sampled at a sub-kilometre scale along the East Pacific Rise between 15°37′N and 15°47′N. The most striking aspect of this signature is its unradiogenic lead (206Pb/204Pb=17.49, 207Pb/204Pb=15.46 and 208Pb/204Pb=36.83). In conjunction with enriched Sr, Nd and Hf signatures, Pb isotopes depict mixing lines that trend away from any known mantle end-members. We suggest that this unradiogenic lead component sampled by magmatic melts corresponds to a novel upper mantle reservoir that should be considered in the Pb isotope budget of the bulk silicate Earth. Major, trace element and isotope compositions are suggestive of an ancient and lower continental origin for this unradiogenic lead component, possibly sulphide-bearing pyroxenites that were preserved even after prolonged stirring within the ambient upper mantle