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The concentrations of halogens in serpentinised olivine-rich lithologies in the lower oceanic crust (e.g. troctolites and wehrlites) and altered-gabbros, recovered from IODP Hole U1309D on the Atlantis Massif of the Mid-Atlantic Ridge, are contrasted. The aims were to evaluate if serpentinisation of lower crustal lithologies could significantly contribute to the volatile budget of oceanic lithosphere and test if serpentinites formed from seawater preserve seawater-like halogen signatures. The olivine-rich lithologies are variably serpentinised by lizardite with minor chrysotile. The maximum concentrations of halogens in the most strongly serpentinised samples are 70 µg/g F, 2,100 µg/g Cl, 9,800 ng/g Br and 8 ng/g I. In comparison, the maxima in interlayered gabbros are 200 µg/g F, 130 µg/g Cl, 400 ng/g Br and 9 ng/g I. The Br/Cl ratios of the altered gabbros are strongly influenced by the presence of amphibole, which preferentially incorporates the smaller halides. The serpentinised lithologies have low F/Cl ratios, due to their strong enrichment in seawater-derived Cl, and they have Br/Cl and I/Cl ratios intermediate of unaltered oceanic crust and seawater-derived fluids. Br/Cl and I/Cl ratios similar to seawater are best preserved in the most Cl-rich samples consistent with these ratios fingerprinting the fluid responsible for serpentinisation. Serpentinites formed from seawater in the lower ocean crust and lithosphere are likely to have low I/Cl ratios. Serpentinsed lithologies in the lower crust (and mantle lithosphere) could, therefore, significantly contribute to halogen subduction helping to explain the range of I/Cl ratios in arc lavas and a proposed decrease of mantle I/Cl over time.

The formation of carbonated serpentinites (serpentine, Mg-Ca carbonates) and listvenites (quartz, Mg-carbonate) by reactions between exhumed mantle peridotites and percolating CO2-bearing fluids is a major sink for carbon from spreading ridges to ophiolites and orogenic suture zones. During ICDP Oman Drilling Project, the transition from the base of the Semail Ophiolite to its metamorphic sole was drilled at Hole BT1B (Wadi Mansah), allowing to recover ~200 m of variously carbonated serpentinites and listvenites, and underlying metabasalts. Mineralogical and geochemical investigations indicate that carbonation at the expense of the Wadi Mansah peridotites was triggered by the migration of multiple fluid batches along the basal thrust at shallow depths and low temperatures (50-250 °C). To better constrain the impacts of fluid source(s) and protolith compositions on reaction pathways and oxidation state during carbonation, we carried out iron and zinc isotopes study of 19 variously carbonated peridotites (13 listvenites, 5 carbonated serpentinites, one serpentinized harzburgite) and of 6 underlying metamorphic samples from Wadi Mansah area (including 3 BT1B samples).The partially serpentinized harzburgite and carbonated serpentinites have δ56Fe and δ66Zn compositions ranging between -0.05 – +0.06 ‰ and -0.11 – +0.15, respectively, overlapping that of previously analysed abyssal (δ56Fe: -0.15 – +0.11 ‰; δ66Zn: +0.12 – +0.62 ‰), ophiolitic (δ56Fe: -0.27 – +0.14 ‰; δ66Zn: -0.56 – +0.38 ‰), orogenic (δ56Fe: -0.06 – +0.12 ‰; δ66Zn: +0.03 – +0.55 ‰), and fore-arc (δ56Fe: -0.26 – +0.09 ‰) peridotites. In contrast, listvenites display highly variable δ56Fe and δ66Zn values, between -0.33 – +0.2 ‰ and -0.46 – +0.64 ‰ respectively. Iron isotopes compositions show a positive correlation with bulk iron contents. Zinc isotope compositions are positively correlated to δ13CTC values, suggesting a high mobility of Zn in carbonate-bearing fluids. The lightest δ66Zn values were measured in listvenites with minor amounts of fuchsite (Cr-mica), that often display evidences for breakdown of Cr-spinel. Metamorphic sole samples display isotopic compositions typical of mafic rocks (δ56Fe: +0.01 – +0.24 ‰; δ66Zn: +0.24 – +0.47 ‰), in agreement with an oceanic crust-derived protolith (MORB, δ56Fe: +0.06 – +0.18; δ66Zn: +0.27 – +0.30 ‰).Our results suggest an important control of the protolith chemistry and complexation with dissolved carbon in reactive fluids on the Fe and Zn isotopes compositions.

International audience; The Oman Drilling Project “Multi-Borehole Observatory” (MBO) samples an area of active weathering of tectonically exposed peridotite. This article reviews the geology of the MBO region, summarizes recent research, and provides new data constraining ongoing alteration. Host rocks are partially to completely serpentinized, residual mantle harzburgites, and replacive. Dunites show evidence for “reactive fractionation,” in which cooling, crystallizing magmas reacted with older residues of melting. Harzburgites and dunites are 65%–100% hydrated. Ferric to total iron ratios vary from 50% to 90%. In Hole BA1B, alteration extent decreases with depth. Gradients in water and core composition are correlated. Serpentine veins are intergrown with, and cut, carbonate veins with measurable 14C. Ongoing hydration is accompanied by SiO2 addition. Sulfur enrichment in Hole BA1B may result from oxidative leaching of sulfur from the upper 30 m, coupled with sulfate reduction and sulfide precipitation at 30–150 m. Oxygen fugacity deep in Holes BA3A, NSHQ14, and BA2A is fixed by the reaction 2H2O = 2H2 + O2 combined with oxidation of ferrous iron in serpentine, brucite, and olivine. fO2 deep in Holes BA1A, BA1D, and BA4A is 3–4 log units above the H2O-H2 limit, controlled by equilibria involving serpentine and brucite. Variations in alteration are correlated with texture, with reduced, low SiO2 assemblages in mesh cores recording very low water/rock ratios, juxtaposed with adjacent veins recording much higher ratios. The proportion of reduced mesh cores versus oxidized veins increases with depth, and the difference in fO2 recorded in cores and veins decreases with depth.

International audience; The composition of the intrusive gabbroic lower oceanic crust remains poorly characterized in comparison to the extrusive portion of the oceanic crust, especially for intermediate-fast spreading mid-ocean ridges. This is a consequence of limited exposures of extant lower oceanic crust or ophiolites similar to mid-ocean ridge crust. One of the best analogues for mid-ocean ridge crust is the southern Samail ophiolite that formed during a period of rapid seafloor spreading above a nascent subduction zone. Here, we focus on the geochemical stratigraphy (whole rock and mineral major and trace element compositions) of the 5,200 m-thick, lower crustal, Wadi Khafifah section of the Wadin Tayin massif in the southern Samail (Oman) ophiolite. Gabbros from the lowermost 3,700 m of this section (the “lower gabbros”) show no systematic changes in composition with height above the Mantle Transition Zone. In contrast, gabbros from the uppermost 1,500 m (the “upper gabbros”) display marked increases in incompatible trace element concentration with increasing height. Liquids in equilibrium with the lower gabbros have major and trace element compositions that overlap with those measured in the upper gabbros and sheeted dikes. Upper gabbros preserve mineral cores with primitive major element compositions that overlap with the range of lower gabbros; however, upper gabbro whole rock compositions are significantly more enriched in incompatible trace elements relative to the lower gabbros. Our data reveal that the upper gabbros are a composite of accumulated minerals derived from primitive melts and a large fraction of evolved melts derived from the fractionation of the lower gabbros. We propose a new “Full Sheeted Sills” model for the lower oceanic crust in which primitive magmas from the mantle are emplaced throughout the lower crust and crystallized in situ. After diking events, evolved magmas leave the lower gabbros and replenish the upper gabbros, thereby contributing to the higher incompatible trace element budget in the upper gabbros relative to the lower gabbros. Our reconstructed bulk compositions of the lower plutonic crust and the bulk oceanic crust from the Wadi Khafifah section yield a plausible primary mantle-derived magma composition in equilibrium with depleted mid-ocean ridge basalts mantle.

International audience; We characterized the texture, composition, and seismic properties of the lithospheric mantle atop the Hawaiian plume by petrostructural analysis of 48 spinel peridotite xenoliths from four localities in three Hawaiian islands. Coarse-porphyroclastic peridotites with variable degrees of recrystallization, recorded by growth of strain-free neoblasts onto the deformed microstructure, predominate. Full evolution of this process produced equigranular microstructures. Some peridotites have coarse-granular microstructures. Coarse-granular and coarse-porphyroclastic peridotites have strong orthorhombic or axial-[100] olivine crystal-preferred orientations (CPOs). Recrystallization produced some dispersion and, locally, changed the olivine CPO towards axial-[010]. Enrichment in pyroxenes relative to model melting trends and pyroxenes with interstitial shapes and CPO uncorrelated with the olivine CPO imply refertilization by reactive melt percolation. The unusual spatial distribution of the recrystallized fraction, Ti enrichment, and Rare Earth Element fractionation in recrystallized, equigranular, and coarse-granular peridotites support that these microstructures are produced by static recrystallization triggered by melt percolation. However, there is no simple relation between microstructure and chemical or modal composition. This, together with marked variations in mineral chemistry among samples, implies multiple spatially heterogeneous melt-rock reaction events. We interpret the coarse-porphyroclastic microstructures and CPO as representative of the original oceanic lithosphere fabric. Annealing changed the microstructure to coarse-granular, but did not modify significantly the olivine CPO. Recrystallization produced moderate dispersion of the CPO. "Normal" oceanic lithosphere seismic anisotropy patterns are therefore preserved. Yet Fe enrichment, refertilization, and limited heating of the base of the lithosphere may reduce seismic velocities by up to 2%, partially explaining negative velocity anomalies imaged at lithospheric depths beneath Hawaii.

The oceanic crust, covering two-thirds of the Earth's surface, is formed along mid-oceanic ridges by crystallization at shallow levels of melts formed at depth by partial melting of mantle peridotite. Yet, the process of melt transport to the ridge axis remains poorly understood. Ophiolites, which provide a window into the uppermost mantle, contain dunite bodies often interpreted as relics of melt flow conduits, formed by pyroxene dissolution during melt-peridotite interaction. Here, we present structural and geochemical data on peridotites from the southeastern Oman ophiolite where three types of dunite, corresponding to the Moho transition zone (MTZ), the main and basal mantle sections, are identified. We focus on osmium isotopes, which are particularly well-adapted to tracing melt flow through peridotites. Osmium isotope signatures from host harzburgites accord with abyssal peridotite values and do not vary systematically with setting. In contrast, dunite Os compositions depend on structural context. Basal dunites display compositions similar to harzburgite values, while MTZ dunites have highly radiogenic compositions similar to those of the overlying crust, requiring extensive interaction with melts more radiogenic than MORB. Modeling shows that melts percolating through and equilibrating with dunite channels would acquire unradiogenic compositions, inconsistent with the observed Os signatures of MTZ dunites and lower crust. Thus, our findings require melt transport without equilibration with dunite or harzburgite, arguing for rapid or at least chemically isolated melt migration from the mantle source to the Moho.

International audience; Although the axial melt lens (AML) beneath fast-spreading mid-ocean ridges has been detected by seismic reflection for decades, its nature and role in the accretion of lower oceanic crust and the evolution and eruption of mid-ocean ridge basalts (MORB) are still poorly constrained. Plutonic rocks consisting of quartz-bearing gabbros, diorites and tonalites, which might represent the upper part of a fossilized AML, have for the first time been recovered from an intact fast-spreading oceanic crust section by Integrated Ocean Drilling Program (IODP) Hole 1256D. Whole-rock major elements show a wide and continuous compositional range (e.g. Mg# 24–70) and apparent enrichments in Ti and Fe at intermediate MgO contents (4–6 wt %). Trace element characteristics are coherent for the different lithology groups defined by petrography and mineral modes; that is, gabbro, clinopyroxene-rich diorite, amphibole-rich or oxide-rich diorite and tonalite. The gabbros and diorites are consistent with modeled products of MORB fractional crystallization, composed of mixed melt and cumulate in varying ratios. Modeled trace elements (especially with respect to Eu) support a model in which the tonalites originated from low-degree partial melting of the sheeted dikes overlying the AML, rather than extreme fractional crystallization. Enrichments in rare earth elements (REE) in clinopyroxenes from the gabbroic and dioritic intrusive rocks suggest strong assimilation of REE-rich tonalitic components by evolved MORB magmas. Hydrothermal alteration was pervasive during cooling of the plutonic system, which can be traced by petrography, mineral compositions and bulk-rock geochemistry. The upper part of AML, largely composed of low-density and high-viscosity felsic magmas, may serve as a barrier to eruptible MORB melts in the lower part of AML.

Microbathymetry data, in situ observations, and sampling along the 13°20′N and 13°20′N oceanic core complexes (OCCs) reveal mechanisms of detachment fault denudation at the seafloor, links between tectonic extension and mass wasting, and expose the nature of corrugations, ubiquitous at OCCs. In the initial stages of detachment faulting and high-angle fault, scarps show extensive mass wasting that reduces their slope. Flexural rotation further lowers scarp slope, hinders mass wasting, resulting in morphologically complex chaotic terrain between the breakaway and the denuded corrugated surface. Extension and drag along the fault plane uplifts a wedge of hangingwall material (apron). The detachment surface emerges along a continuous moat that sheds rocks and covers it with unconsolidated rubble, while local slumping emplaces rubble ridges overlying corrugations. The detachment fault zone is a set of anostomosed slip planes, elongated in the along-extension direction. Slip planes bind fault rock bodies defining the corrugations observed in microbathymetry and sonar. Fault planes with extension-parallel stria are exposed along corrugation flanks, where the rubble cover is shed. Detachment fault rocks are primarily basalt fault breccia at 13°20′N OCC, and gabbro and peridotite at 13°30′N, demonstrating that brittle strain localization in shallow lithosphere form corrugations, regardless of lithologies in the detachment zone. Finally, faulting and volcanism dismember the 13°30′N OCC, with widespread present and past hydrothermal activity (Semenov fields), while the Irinovskoe hydrothermal field at the 13°20′N core complex suggests a magmatic source within the footwall. These results confirm the ubiquitous relationship between hydrothermal activity and oceanic detachment formation and evolution.

International audience; nternational Ocean Discovery Program (IODP) Expedition 352 recovered a high-fidelity record of volcanism related to subduction initiation in the Bonin fore-arc. Two sites (U1440 and U1441) located in deep water nearer to the trench recovered basalts and related rocks; two sites (U1439 and U1442) located in shallower water further from the trench recovered boninites and related rocks. Drilling in both areas ended in dolerites inferred to be sheeted intrusive rocks. The basalts apparently erupted immediately after subduction initiation and have compositions similar to those of the most depleted basalts generated by rapid sea-floor spreading at mid-ocean ridges, with little or no slab input. Subsequent melting to generate boninites involved more depleted mantle and hotter and deeper subducted components as subduction progressed and volcanism migrated away from the trench. This volcanic sequence is akin to that recorded by many ophiolites, supporting a direct link between subduction initiation, fore-arc spreading, and ophiolite genesis.

International audience; The building of oceanic crust at Oceanic Core Complexes (OCC) has been described as a complex process involving multiple intrusions of magma over a protracted period of time. The migration of primitive magmas (i.e., Mid Ocean Ridge Basalts, MORBs) can lead to melt-rock interactions during reactive porous flow processes through the lithosphere. The timescales of these reactive processes and the subsequent cooling of the modified crystal matrix remain unconstrained. Diffusion modelling has beenwidely used to retrieve timescales of magmatic processes. In this study, we use diffusion models to constrain (i) the minimum timescales of melt-rock interactions and (ii) the cooling rates of the gabbroic sequence forming the oceanic crust at an OCC.We chose samples of the most primitive olivine-rich troctolites fromthe gabbroic sequence sampled in IODP Hole U1309D (AtlantisMassif OCC, Mid-Atlantic Ridge 30°N). Olivine-rich troctolites were interpreted as marking local partial assimilation of mantle intervals into the oceanic crust, and thus allowed to understand the dynamics of mantle assimilation and the formation of slow-spreading oceanic crust at the Atlantis Massif OCC. Olivines in olivine-rich troctolites represent relicts of pre-existing mantle olivine, while clinopyroxenes and plagioclases are crystallized during reactive percolation. Olivine chemical compositions show that olivine-rich troctolites inherit chemical heterogeneity from the mantle precursor. Flat geochemical profiles in olivine indicate complete chemical re-equilibration of olivine crystals with the locally modified percolating melt. Exception is made for most Ca profiles that show lower Ca contents at the olivine rim compared to the relative crystal core, as the result of subsolidus cooling. Three-dimensional (3D) diffusion models at magmatic conditions (T = 1210–1300 °C and P = 2 kbar) reveal that complete chemical re-equilibration of 4 mm-size mantle-derived olivine with percolating MORB-type melts can be attained within durations of less than 300 yr. The Ca-in-olivine geospeedometer reveal that cooling rates from ~1200 °C to ~1050 °C are constant downhole and on average 0.004 °C/yr; they are comparable with lower temperature cooling rates (850 °C–250 °C) estimated at the AtlantisMassif OCC. The minimumtimescales from 3D models point to rather fast re-equilibration of olivine. The downhole chemical heterogeneity inherited from the precursor mantle, coupled with the timescales of diffusive re-equilibration suggest that the partial assimilation of the upwelling mantle and its incorporation into the oceanic crust occurred in the time-frame of a single melt input. Our cooling data are consistentwith building of the oceanic crust at OCCs controlled by continuous uplift, in turn governed by long-lived detachment faults. The latter contribute to the rapid cooling of the assimilated mantle intervals and the magma bodies. Diffusion models of geochemical profiles in olivine from a single crustal section allow to reconstitute the early magmatic processes leading to mantle assimilation and early crystallization of gabbros, and the cooling history of the oceanic crust at OCC from magmatic conditions to hydrothermalism.

Tectonic mixing of slab- and mantle-derived materials at the interface between converging plates highly enhances fluid-mediated mass transfer from the slab to the overlying mantle. Subduction mélanges can provide information about the interaction among different slices accreted at plate interface domains, with implications on the tectonic and geochemical evolution of the plate-interface itself. At Cima di Gagnone, pelitic schists andgneissenclose chloriteharzburgiteandgarnetperidotitelenses, like in subduction mélanges located in-between downgoing slabs and overlying mantle. These peridotites host MORB-typeeclogiteand metarodingite, and derive from dehydration of serpentinized mantleprotoliths. Their enrichment in fluid-mobile B, As, Sb, U, Th is the result of an early-stage oceanicserpentinization, followed by interaction with hostmetasedimentsduring subduction burial. Here we define the element exchange process in the Gagnone mélange by means of the B, Sr and Pb isotope analysis of its main lithologies (ultramafic,mafic rocksand paragneiss). The87Sr/86Sr and206Pb/204Pb ratios ofultramafic rocks(0.7090–0.7124 and 18.292–18.837, respectively) show enrichments in radiogenic Sr and Pb after exchange with the host paraschist (up to 0.728787Sr/86Sr; 18.751206Pb/204Pb). The δ11B values of peridotites (down to −10‰) point to a combined effect of (1)11B release to deserpentinization fluids (serpentinized protoliths likely had positive δ11B and lower radiogenic Sr, Pb), and of (2) exchange with fluids from the surrounding metasediments. The whole Gagnone rock-suite is finally overprinted by retrograde fluids that essentially bring to an increase in radiogenic Pb (about 19.0206Pb/204Pb) and to values of 0.71087Sr/86Sr and of −10‰ δ11B. The recognition of different stages of interaction between mantle rocks and sedimentary/crustal reservoirs allows us to define the geochemical effects related to the early coupling of such rocks along the plate-interface. Our study shows that ultramafic rocks involved in subduction-zonemetamorphismand serpentinization uptake radiogenic Pb and Sr released by associated sedimentary reservoirs. The exchange process envisioned here is not only representative of subduction mélanges: it can also be a proxy of mass transfer between slab and serpentinized supra-subduction mantle, as occurs in forearcs. Dehydration of the Gagnone-type serpentinized mantle releases crust-derived components to arcs, without direct involvement of metasediment dehydration and/or melting in subarc environments. The retention of appreciable amounts of fluid-mobile elements, radiogenic Pb and Sr in dehydrated Gagnone peridotites has implications on element recycling in the deep Earth’s mantle.

International audience; Deep melt intrusion and melt-peridotite interaction may introduce small-scale heterogeneity in the MORB mantle. These processes generate pyroxenite-bearing veined mantle that represent potential mantle sources of oceanic basalts. Natural proxies of such veined mantle are very rare and our understanding of mechanisms governing the chemical modification of mantle peridotite by MORB-type pyroxenite emplacement is very limited. We report the results of detailed spatially-controlled chemical profiles in pyroxenite-peridotite associations from the Northern Apennine ophiolitic mantle sequences (External Liguride Units, Italy), and investigate the extent and mechanism driving the local modification of peridotite by the interaction with pyroxenite-derived melt. Pyroxenites occur as cm-thick layers parallel to mantle tectonite foliation and show diffuse orthopyroxene-rich reaction rims along the pyroxenite-peridotite contact. Relative to distal unmodified peridotites, wall-rock peridotites show i) modal orthopyroxene enrichment at the expense of olivine, ii) higher Al, Ca, Si contents and slightly lower XMg, iii) Al-richer spinel and lower-XMg pyroxenes. Clinopyroxenes from wall-rock peridotites exhibit variable LREE-MREE fractionation, always resulting in SmN/NdN ratios lower than distal peridotites. From the contact with pyroxenite layers, peridotite clinopyroxenes record a REE compositional gradient up to about 15 cm marked by an overall REE increase away from the pyroxenite. Beyond 15 cm, and up to 23 cm, the MREE and HREE content decreases while the LREEs remain at nearly constant abundances. This REE gradient is well reproduced by a two-step numerical simulation of reactive melt percolation assuming variable amounts of olivine assimilation and pyroxene crystallization. Percolative reactive flow at decreasing melt mass and rather high instantaneous melt/peridotite ratio (initial porosity of 30%), combined with high extents of fractional crystallization (i.e. relatively low Ma/Mc ratio), accounts for the overall REE enrichment in the first 15 cm. Change of melt-rock reaction regime, mostly determined by the drastic decrease of porosity (Φi = 0.01) due to increasing crystallization rates, results in more efficient chemical buffering of the host peridotite on the HREE composition of the differentiated liquids through ion-exchange chromatographic-type processes, determining the observed increase of the LREE/HREE ratio. Emplacement of thin (cm-sized) pyroxenite veins by deep melt infiltration is able to metasomatize a much larger volume of the host peridotite. Hybrid mantle domains made by pyroxenite, metasomatized peridotite and unmodified peridotite potentially represent mantle sources of E-MORB. Results of this work stress the key role of melt-peridotite reactions in modifying the upwelling mantle prior to oceanic basalts production.

International audience; Over the last decades, numerous studies have emphasized the role of serpentinites in the subduction zone geodynamics. Their presence and role in subduction environments are recognized through geophysical, geochemical and field observations of modern and ancient subduction zones and large amounts of geochemical database of serpentinites have been created. Here, we present a review of the geochemistry of serpentinites, based on the compilation of ~ 900 geochemical data of abyssal, mantle wedge and exhumed serpentinites after subduction. The aim was to better understand the geochemical evolution of these rocks during their subduction as well as their impact in the global geochemical cycle. When studying serpentinites, it is essential to determine their protoliths and their geological history before serpentinization. The geochemical data of serpentinites shows little mobility of compatible and rare earth elements (REE) at the scale of hand-specimen during their serpentinization. Thus, REE abundance can be used to identify the protolith for serpentinites, as well as magmatic processes such as melt/rock interactions before serpentinization. In the case of subducted serpentinites, the interpretation of trace element data is difficult due to the enrichments of light REE, independent of the nature of the protolith. We propose that enrichments are probably not related to serpentinization itself, but mostly due to (sedimentary-derived) fluid/rock interactions within the subduction channel after the serpentinization. It is also possible that the enrichment reflects the geochemical signature of the mantle protolith itself which could derive from the less refractory continental lithosphere exhumed at the ocean-continent transition. Additionally, during the last ten years, numerous analyses have been carried out, notably using in situ approaches, to better constrain the behavior of fluid-mobile elements (FME; e.g. B, Li, Cl, As, Sb, U, Th, Sr) incorporated in serpentine phases. The abundance of these elements provides information related to the fluid/rock interactions during serpentinization and the behavior of FME, from their incorporation to their gradual release during subduction. Serpentinites are considered as a reservoir of the FME in subduction zones and their role, notably on arc magma composition, is underestimated presently in the global geochemical cycle.

International audience; Mid-ocean ridge basalt (MORB) is the most abundant magma on Earth, and provides a geochemical window into the mantle. Deriving mantle composition and melting processes from the erupted lavas requires correction to be made for their evolution as they pass through and generate the oceanic crust. This is typically done by assuming that modification of melts in crustal magma chambers occurs exclusively by fractional crystallisation. However, extensive mineral major- and trace element data from a full section of fast-spread lower crustal rocks exposed in Hess Deep (equatorial Pacific Ocean) demonstrate that their evolution is instead controlled by reactive porous flow. These reactions lead to a strong enrichment in, and fractionation of, incompatible trace elements in the melt (as recorded by clinopyroxene compositions), leading to melt compositions far outside of the compositional realm of MORB both in terms of trace element abundances and ratios. The reactive signature increases in strength up section, peaking in varitextured gabbros interpreted to represent the fossilised axial melt lens, indicating that reactive porous flow occurred on the scale of the entire lower crust. The enrichment of the melt is coupled with a strong trace element depletion of plagioclase, olivine, and, to a lesser extent, clinopyroxene cores, suggesting that these phases represent the residues of the reactions from which trace elements have been removed. The dominant role of reactive porous flow, and the resulting deviations from fractional crystallisation predictions, suggest that the lower oceanic crust plays a much more complex and significant role in modifying the compositions of MORB than previously expected, with consequent implications for models of mantle processes.

The Lanzo peridotite massif is a fragment of oceanic lithosphere generated in an ocean-continent transition context and eclogitized during alpine collision. Despite the subduction history, the massif has preserved its sedimentary oceanic cover, suggesting that it may have preserved its oceanic structure. It is an exceptional case for studying the evolution of a fragment of the lithosphere from its oceanization to its subduction and then exhumation. We present a field and petrological study retracing the different serpentinization episodes and their impact on the massif structure. The Lanzo massif is composed of slightly serpentinized peridotites (

Serpentinization of the oceanic lithosphere contributes significantly to the geochemical cycle from spreading ridges to subduction zones. In situ trace element analysis of oceanic serpentinites from the Mid-Atlantic Ridge and the Greater Antilles (Cuba, Dominican Republic) shows that all serpentine minerals are enriched in fluid-mobile elements (FME: As, Sb, B, Li, Cs, Pb, U, Ba, Sr). We observe no loss of these elements from abyssal to subduction environments during prograde metamorphism. Moreover, the transition from lizardite/chrysotile to antigorite during subduction is marked by a strong over-enrichment in As and Sb in antigorite, indicating late contamination by a sedimentary source. This suggests that a second stage of serpentinization occurs in the earlier stages of subduction, when newly formed or reactivated normal faults ease fluid penetration, and/or in the subduction channel. Our study shows that, from spreading ridges to forearc environments, serpentines act as sponges for FME. We posit that, until ultimate antigorite breakdown, serpentinites efficiently transport significant amounts of FME down to great depths in the mantle.

The Oman ophiolite consists of several massifs cropping out along a 500 km long band trending NW-SE along the coast of Oman; it is one of the best exposed sections of oceanic crust and mantle in the world. There is a gradient in igneous processes and composition in the ophiolite, with the northern massifs recording a polygenetic igneous history involving an increasingly important subduction component, whereas the southern massifs were formed primarily via a mid-ocean ridge basalt (MORB)-like, single-stage process at a submarine spreading ridge. In this study we use geochemical data from Wadi Tayin, which is one of the southern massifs of the Oman ophiolite, to constrain the composition and genesis of oceanic crust and upper mantle. The Wadi Tayin harzburgites are residues of partial melting that are as depleted as the most depleted mid-ocean ridge peridotites. They have low middle- to heavy rare earth element ratios, most probably reflecting melting close to and beyond the exhaustion of clinopyroxene. Like many abyssal peridotites, the Wadi Tayin samples show enrichment in highly incompatible elements, giving rise to U-shaped MORB-normalized trace element patterns. We favor the idea that this is caused by enrichment of highly incompatible elements along grain boundaries in peridotite, which may be the result of near-equilibrium partitioning between grain boundaries and grain interiors, rather than disequilibrium processes. Equilibrium partitioning between crystals and grain boundaries during melting and melt extraction is also our preferred explanation for ubiquitous high Pb contents relative to Ce and La in our samples as well as in most abyssal peridotites. The Wadi Tayin samples record substantial variability in terms of osmium isotopic composition and platinum group element (PGE) concentrations. The more radiogenic nature of the dunites and impregnated peridotites compared with the residual harzburgites may be due to relatively high Os-187/Os-188 in melt transported through the dunites. The presence of residual peridotites with whole-rock osmium isotopic compositions less radiogenic than MORB may be explained by melting of a veined (upwelling) mantle forming mixed melts in which much of the Os derives from veins with high Re/Os in a matrix of previously depleted peridotite. An important result of this study is that the shallowest samples are refertilized (i.e. anomalously enriched in incompatible elements), and record relatively high metamorphic closure temperatures. These observations suggest that migrating melt underwent crystallization during rapid cooling in the uppermost mantle during and immediately after ridge magmatism. A variety of geothermometers all yield the result that the stratigraphically highest harzburgites equilibrated at higher temperature than the deeper ones. The systematic decrease in closure temperature with increasing depth below the Moho transition zone probably reflects systematic variation in cooling rate as a function of depth in the mantle section. We hypothesize that the refertilization and higher closure temperatures recorded by the uppermost mantle samples are linked. More rapid cooling led to higher closure temperatures, and to partial crystallization of migrating melts in the shallowest part of the mantle section, yielding slightly elevated abundances of elements such as Ca and Na, and incompatible trace elements.

Seismic anisotropy in subduction zones results from a combination of various processes. Although it depends primarily on the orientation of olivine in response to flow, the presence of water and melt in the wedge may modify the deformation of olivine. The melt distribution also influences anisotropy. Direct observations of the deformation and melt-rock interactions in a strongly depleted spinel-harzburgite massif from the Cache Creek terrane in the Canadian Cordillera allow evaluating the relative contribution of each process. Structural mapping shows that this massif has recorded high-temperature, low-stress deformation, high degrees of partial melting, and synkinematic melt-rock interaction at shallow depths (

Abyssal peridotite from the 15°20′N area of the Mid-Atlantic Ridge show complex geochemical variations among the different sites drilled during ODP Leg 209. Major element compositions indicate variable degrees of melt depletion and refertilization as well as local hydrothermal metasomatism. Strongest evidence for melt–rock interactions are correlated Light Rare Earth Element (LREE) and High Field Strength Element (HFSE) additions at Sites 1270 and 1271. In contrast, hydrothermal alteration at Sites 1274, 1272, and 1268 causes LREE mobility associated with minor HFSE variability, reflecting the low solubility of HFSE in aqueous solutions. Site 1274 contains the least-altered, highly refractory, peridotite with strong depletion in LREE and shows a gradual increase in the intensity of isochemical serpentinization; except for the addition of H 2 O which causes a mass gain of up to 20 g/100 g. The formation of magnetite is reflected in decreasing Fe 2+ /Fe 3+ ratios. This style of alteration is referred to as rock-dominated serpentinization. In contrast, fluid-dominated serpentinization at Site 1268 is characterized by gains in sulfur and development of U-shaped REE pattern with strong positive Eu anomalies which are also characteristic for hot (350 to 400 °C) vent-type fluids discharging from black smoker fields. Serpentinites at Site 1268 were overprinted by talc alteration under static conditions due to interaction with high a SiO 2 fluids causing the development of smooth, LREE enriched patterns with pronounced negative Eu anomalies. These results show that hydrothermal fluid–peridotite and fluid–serpentinite interaction processes are an important factor regarding the budget of exchange processes between the lithosphere and the hydrosphere in slow spreading environments.

In addition to thermal erosion, plume/lithosphere interaction may induce significant changes in the lithosphere chemical composition. To constrain the extent of this process in an oceanic environment and its consequences on the lithosphere seismic properties, we investigated the relationship between petrological processes and microstructure in mantle xenoliths from different hotspots tracks in South Pacific Superswell region: the Austral-Cook, Society, and Marquesas islands in French Polynesia. Olivine forsterite contents in the studied spinel peridotites vary continuously from Fo91 to Fo83. Dunites and wehrlites display the lowest forsterite contents. Their microstructure and high Ni contents preclude a cumulate origin, suggesting that these rocks result from melt/rock reactions involving olivine precipitation and pyroxene dissolution. In addition, lherzolites and wehrlites display evidence of late crystallization of clinopyroxene, which may result from a nearsolidus melt–freezing reaction. These data suggest that the lithosphere above a mantle plume undergoes a complex sequence of magmatic processes that significantly change its composition. These compositional changes, particularly iron enrichment in olivine, result in lower P- and S-waves velocities. Relative to normal lithospheric mantle, compositionally induced seismic anomalies may attain 2.2% for S-waves and 1% for P-waves. Smaller negative anomalies for P-waves are due to a higher sensitivity to modal composition. Conversely, crystal-preferred orientations (CPO) and seismic anisotropy are little affected by these processes. Lherzolites and harzburgites, independent from composition, show high-temperature porphyroclastic microstructures and strong olivine CPO. Dunites and wehrlites display annealing microstructures to which is associated a progressive dispersion of the olivine CPO. Very weak, almost random olivine CPO is nevertheless rare, suggesting

The compositions of glass clasts in volcaniclastic rocks recovered from drilling at Site 1184 on the eastern salient of the Ontong Java Plateau (OJP) are investigated using microbeam analytical methods for major, minor and trace elements. These data are com- pared with whole-rock elemental and isotopic data for bulk tuff samples, and with data from basalts on the high plateau of the OJP. Three subunits of Hole 1184A contain blocky glass clasts, thought to represent the juvenile magmatic component of the phreatomagmatic eruptions that generated the volcaniclastic rocks. The glass clasts have unaltered centres, and are all basaltic low-K tholeiites, with flat chondrite-normalized rare earth element (REE) patterns. Their elemental compositions are very similar to the Kwaimbaita-type and Kroenke-type basalts sampled on the high plateau. Each subunit has a distinct glass com- position and there is no intermixing of glass compositions between subunits, indicating that each subunit is the result of one eruptive phase, and that the volcaniclastic sequence has not experienced reworking. The relative heterogeneity preserved at Site 1184 contrasts with the uniformity of compositions recovered from individual sites on the high plateau, and suggests that the eastern salient of the OJP had a different type of magma plumbing system. Our data support the hypothesis that the voluminous subaerially erupted volcani- clastic rocks at Site 1184 belong to the same magmatic event as the construction of the main Ontong Java Plateau. Thus, the OJP would have been responsible for volatile fluxes into the atmosphere in addition to chemical fluxes into the oceans, and these factors may have influenced the contemporaneous oceanic anoxic event.

The objectives for Expedition 352 were to drill through the entire volcanic sequence of the Bonin fore arc to 1. Obtain a high-fidelity record of magmatic evolution during subduction initiation and early arc development, 2. Test the hypothesis that fore-arc basalt lies beneath boninite and understand chemical gradients within these units and across the transition, 3. Use drilling results to understand how mantle melting processes evolve during and after subduction initiation, and 4. Test the hypothesis that the fore-arc lithosphere created during subduction initiation is the birthplace of suprasubduction zone (SSZ) ophiolites. Expedition 352 successfully cored 1.22 km of igneous basement and 0.46 km of over-lying sediment, providing diverse, stratigraphically controlled suites of fore-arc basalts (FAB) and boninite related to seafloor spreading and earliest arc development. FAB were recovered at the two deeper water sites (U1440 and U1441) and boninites at the two sites (U1439 and U1442) drilled upslope to the west. FAB lavas and dikes are depleted in high-field strength trace elements such as Ti and Zr relative to mid-ocean-ridge basalt but have relatively diverse concentrations of trace elements bezcause of variation in degrees of melting and amount of subducted fluids involved in their genesis. All FAB magmas underwent significant crystal fractionation in a persistent magma chamber system. Holes U1439C and U1442A yielded entirely boninitic lavas. We defined three boninite differentiation series based on variations in MgO, SiO2, and TiO2 concentrations of the parental magmas. Lavas in both pairs of holes have compositions that generally become more primitive and have lower TiO2 concentrations upward. The presence of dikes at the base of the sections at Sites U1439 and U1440 provides evidence that boninitic and FAB lavas are both underlain by their own conduit systems and that FAB and boninite group lavas are likely offset more horizontally than vertically. We thus propose that seafloor spreading related to subduction initiation migrated from east to west after subduction initiation and during early arc development. Initial spreading was likely rapid, and an axial magma chamber was present. Melting was largely decompressional during this period, but subducted fluids affected some melting. As subduction continued and spreading migrated to the west, the embryonic mantle wedge became more depleted, and the influence of subducted constituents dramatically increased, causing the oceanic crust to be built of boninitic rather than tholeiitic magma. The general decrease in fractionation upward reflects the eventual disappearance of persistent magma chambers, either because spreading rate was decreasing with distance from the trench or because spreading was succeeded by off-axis magmatism trenchward of the ridge. The extreme depletion of the sources for all boninitic lavas was likely related to the incorporation of mantle residues from FAB generation. This mantle depletion continued during generation of lower silica boninitic magmas, exhausting clinopyroxene from the mantle such that the capping high-Si, low-Ti boninites were generated from harzburgite. Additional results of the cruise include recovery of Eocene to recent deep-sea sediment that records variation in sedimentation rates with time resulting from variations in climate, the position of the carbonate compensation depth, and local structural control. Three phases of highly explosive volcanism (latest Pliocene to Pleistocene, late Miocene to earliest Pliocene, and Oligocene) were identified, represented by 132 graded air fall tephra layers. Structures found in the cores and reflected in seismic profiles show that this area had periods of normal, reverse, and strike-slip faulting. Finally, basement rock P-wave velocities were shown to be slower than those observed during logging of normal ocean crust sites.

The Oman ophiolite exposes a large and well-preserved mantle section beneath a palaeo-spreading centre. The mantle section is mainly composed of extremely refractory harzburgites with relatively homogeneous modal and major element compositions. Nevertheless, our trace element data exhibit variations connected with the main mantle structures, which allow us to define three geochemical and structural domains. The main harzburgitic mantle section, mainly constituted of strongly refractory harzburgites characterised by chondrite-normalised REE patterns that are steadily depleted from HREE to LREE. These rocks are interpreted as mantle residues after s 15% melt extraction. Their REE signature can be explained by melt transport associated with partial melting. The diapir areas (mainly the Maqsad diapir), defined by plunging lineations. They are constituted of harzburgites with roughly the same modal composition as the main mantle section but distinct, concave-upward REE patterns. The regions of most active upwelling (characterised by sub-vertical lineations) are further distinguished by higher Al2O3/CaO ratios and TiO2 contents. This character is ascribed to focused partial melt upwelling. The diapirs are interpreted as local instabilities in upwelling mantle, possibly triggered by feedback mechanisms between deformation and melt percolation. The Maqsad diapir is topped by a thick, dunitic, mantle^crust transition zone (MTZ) that displays the same trace-element signature as the diapir. However, the dunites are distinguished by low Mg# values and Ni contents. Together with structural evidence, this allows us to interpret the MTZ dunites as diapir harzburgites that were strongly modified by olivine-forming melt^rock reactions at high melt/ rock ratios. The MTZ is thought to act as a major collecting zone for mantle melts. The cpx-harzburgites from the base of the mantle section. These rocks are distinguished by high clinopyroxene contents (s 5%), low AL2O3/CaO and ‘spoon-shaped’ REE patterns. They were individualised from the rest of the harzburgite mantle section by a cpxforming melt^rock reaction at decreasing malt mass. This reaction probably occurred at near-solidus conditions along the lithosphere^asthenosphere boundary. The formation of these three domains may be integrated in a geodynamic scenario involving the reactivation of an oceanic lithosphere, a process that would be related to the ridge propagator identified in the Oman ophiolite. fl 2000 Elsevier Science B.V. All rights reserved.

The eastern end of the Haylayn massif exposes a complex paleoridge structure interpreted as the tip of a northwestward propagating segment (Nicolas et al., this issue). The area, revisited from a petrostructural and geochemical viewpoint, offers the most documented exposures of the association of olivine gabbros and gabbronorites in Oman (Juteau et al., 1988). Gabbronorites were injected while the main gabbro unit was deforming in the magmatic state. Both units do not differ chemically, except for the SiO2 enrichment of the orthopyroxene-rich gabbros relative to olivine-gabbro. In addition, they display the same trace element signature, which implies the same parent magma for both units. The extension of the stability field of orthopyroxene is assigned to increase of oxygen fugacity due to hydration. The source of hydration is the ridge axis hydrothermal circulation, suggesting hydrothermal/magma interaction at temperatures above the gabbro solidus. The distribution of gabbronorites at the scale of the entire ophiolite suggests a relation with ridge tectonics where high-T conditions of hydrothermal-magmatic interaction are met. Such conditions are met when propagating segments rotate the structures of the dying magma chamber.

As opposed to ocean crustal drilling that often yields a discontinuous core, ophiolites provide a unique opportunity to study continuous sections of oceanic basalts. In order to provide high frequency constraints on the construction of the upper oceanic crust, a continuous 280 m thick volcanic transect was sampled in the Semail ophiolite in Oman. The analyzed section is located in the Sarami Massif, in the central part of the ophiolite, and exposed along Wadi Shaffan. A multidisciplinary study was carried out after sampling in the field. Core measurements including porosity, grain density, compressional velocity, magnetic susceptibility and electrical resistivity for over 100 samples from this transect have been made. Geochemical analyses including major, trace and Rare Earth Elements were also performed on 23 selected samples from this transect. The Wadi Shaffan transect appears as composed of two main petrological and geochemical members providing the main lithostratigraphic signal. The boundary between the two sequences is marked by the presence of a massive flow unit equating to the most primitive lava and across which significant changes in mineralogy and texture are observed. The physical properties equally record significant changes. In all, the section is characterized by chemical compositions coherent with that of V1-Geotime volcanism and appears as built through two main sequences of volcanic activity. The magnetic susceptibility profile correlated to geochemical variations present the most detailed evolution allowing to individualize a succession of at least 4 volcanic phases. These phases are interpreted as magmatic cycles characterized by differentiation processes, allowing one to place high frequency constraints on the volcanic behavior of fast spreading ridges. Some of the physical properties also reflect this series of differentiation trends, as noticed in the past from downhole measurements recorded in the context of deep ocean drilling into the crust.

International audience; During the last decade, Integrated Ocean Drilling Program (IODP) has made substantial progress in sampling the deeper parts of the ocean crust (>1 km below seafloor). Holes into slow-spread Atlantic ocean crust at Site U1309 and fast-spread Pacific crust at Site 1256 shed light on important unknown and poorly understood aspects of the architecture and accretion of modern ocean crust. Recent drilling into Pacific lower crust tectonically exposed at Hess Deep also provides new insights (Site U1415). Key observations and findings include the possible implication of mantle rocks in magmatic accretion of the lower crust at slow-spreading ridges, the confirmation that the development of oceanic core complexes via detachment faulting involves tectonic rotation of the footwall, a detailed and comprehensive picture of the complex interplay between magmatic, metamorphic, and hydrothermal processes at the base of the sheeted dike complex at fast-spreading ridges, and the first sampling of significant sections of layered gabbros in fast-spread lower crust.

Mantle rock studies provide evidence of interaction with upwelling magmas. In erogenic lherzolites, one of the most conspicuous effects of these interactions is the development of harzburgite and dunite bands. Recent studies have suggested that these bands were formed at the expense of the host lherzolites by melt-rock reactions associated with magma percolation. In order to better understand the geochemical effects associated with percolation-reaction processes, we propose a numerical model of melt infiltration that takes into account modal variations in time and space resulting from melt-rock reactions. Melt volume variations are considered by means of porosity variations, and a local equilibrium approach is used for trace element exchange between melt and minerals. The transport of trace elements by the interstitial melt is described by a mass balance equation while the modal variations are constrained by the mineralogical trends observed in refractory peridotites massifs. The model is applied to RBE, Cr and Ni in percolated peridotites affected by an olivine-forming reaction, with the aim of reproducing the evolution of these elements in refractory peridotites from the Ronda massif. Our modelling can explain the negative correlation between the LREE/HREE ratio and the HREE content and between Cr and Ni in the Ronda refractory peridotites. Our results validate the hypothesis that, in the Ronda, the bands of refractory peridotites represent porous-flow channels formed by olivine-forming melt-rock reaction, at increasing melt volume. Because similar geochemical features are observed in ophiolitic peridotites and in mantle xenoliths, it is likely that melt-rock reactions associated with magmatic infiltration are widespread and represent important mantle processes.

Expedition 335 of the riserless drilling platform Puntarenas, Costa Rica, to Balboa, Panama Site 1256 13 April-3 June 2011

International audience; Serpentinites from subduction environments represent an important sink for fluid-mobile elements. In order to constrain geochemical behavior of fluid-mobile elements hosted by serpentine phases during subduction processes, we carried out a geochemical study (trace elements and Pb isotopes) of a series of serpentinites and cumulates from the accretionary wedge of Greater Caribbean (Cuba and Dominican Republic). The trace element compositions of the primary and alteration-related phases were analyzed in situ using LA-HR-ICP-MS techniques. The studied samples represent parts of the subducted proto-Atlantic oceanic lithosphere, which has experienced low to high grade metamorphism (greenschist to eclogite facies), before being exhumed; a subset of these samples were derived from the mantle wedge. This sampling provides the opportunity to trace the chemical mobility of fluid-mobile elements during prograde metamorphism along a cold geotherm in an oceanic subduction setting.

The 1415 m deep IODP Hole U1309D (Mid-Atlantic Ridge, 30 degrees N) is the second deepest hole drilled into slow spreading oceanic lithosphere. The recovered section comprises essentially gabbroic rocks, with a large range of compositions. The most primitive end-members of the gabbroic sequence, herein referred to as olivine-rich troctolites (ol > similar to 70%), have textures and geochemical compositions intermediate between that of mantle peridotites and primitive cumulates, indicative of melt impregnation processes. We carried out a detailed microstructural study to further characterize the petrogenetic processes leading to their formation, as well as discuss their mode of emplacement and relationship with neighboring mantle lithosphere. In olivine-rich troctolites, olivines range from coarse-grained subhedral crystals, commonly containing well-developed subgrains, to medium-grained rounded crystals with fewer or no substructures. They are embedded in large, undeformed pyroxene and plagioclase poikiloblasts. Olivine substructures reveal dislocation creep that is consistent with activation of the main high-temperature slip systems, dominantly (010)[100]. Olivine crystallographic preferred orientation is very weak but generally shows a relatively stronger, uncommon [001] concentration. These unusual olivine fabrics are interpreted as resulting from melt impregnation of a previously deformed olivine matrix: the solid olivine framework is disrupted by olivine corrosion along grain and subgrain boundaries, and the high-temperature plastic fabric is modified in a liquid-dominated regime. Based on mineral composition and fabrics and in comparison with what is observed in impregnated mantle rocks elsewhere, we posit that olivine represents relicts of mantle peridotites disaggregated by large melt influx, although the mantle origin of olivine is not unequivocally demonstrated yet. Whatever the initial lithology, impregnation by large volumes of melt has strongly modified the original composition and microstructure. If the mantle origin hypothesis is correct, the original olivine fabric could have been efficiently weakened by dunitization prior to disruption of the olivine framework by melt impregnation. Incorporation, at the base of the lithosphere, of small slivers of impregnated dunite into gabbroic sections, trapped between successive igneous units, may be a common mechanism of lower crustal accretion at slow spreading ridges. Extensive melt-rock interaction processes are expected to contribute significantly to the final chemical composition of erupted lavas.