FLUID IN CONVERGENT MARGIN SYSTEMS

[1] A comprehensive geochemical study, including B, Pb, Sr, and Nd isotopes, has been carried out on El Salvador subduction-related lavas. The rocks have arc-type incompatible element distributions with high LILE/HFSE ratios, nearly constant 143Nd/144Nd (≈0.5130), and small differences in 207Pb/204Pb (15.53–15.57), whereas 87Sr/86Sr ranges from 0.7035 to 0.7039. Boron isotopic composition varies widely, between −2.7‰ and +6.3‰. The boron isotope signature points to involvement of fluid inputs from (1) a high-δ11B serpentinite fluid from serpentized mantle wedge dragged beneath the volcanic arc or from the subducting lithosphere and (2) a low-δ11B fluid from the progressive dehydration of subducted altered basaltic crust and/or sediments. The observed sample variability is explained with a model in which different proportions of serpentinite-derived (10–50%) and slab-derived fluids are added to an enriched-DMM source, triggering its partial melting. We suggest a model in which tectonic erosion, i.e., dragging down of slivers of serpentinized upper plate mantle, was responsible for the occurrence of serpentinite reservoir, 11B-enriched in the forearc by shallow fluids

Syros Metasomatic Tourmaline: Evidence for Very High-δ11B Fluids in Subduction Zones

High-pressure (HP) metamorphic blocks enclosed in a mafic to ultramafic matrix from a mélange on the island of Syros are rimmed by tourmaline-bearing reaction zones (blackwalls). The B isotopic composition of dravitic tourmaline within these blackwalls was investigated in situ by secondary ion mass spectrometry. Boron in these tourmalines is unusually heavy, with δ11B values exceeding +18‰ in all investigated samples and reaching an extreme value of +28·4‰ in one sample. Blackwalls formed during exhumation of the HP mélange at a depth of 20-25 km at temperatures of 400-430°C, by influx of external hydrous fluids. The compositions of the fluids are estimated to be in the range of 100-300 μg/g B with δ11B values of +18 to +28‰. The high δ11B values cannot be explained by tourmaline formation from unmodified slab-derived fluids. However, such fluids could interact with the material in the exhumation channel on their way from the dehydrating slab to the site of tourmaline formation in the blackwalls. This could produce exceptionally high δ11B values in the fluids, a case that is modelled in this study. The model demonstrates that subduction fluids may be effectively modified in both trace element and isotopic composition during their migration through the material overlying the subducting slab. Blackwall tourmaline from Syros has a large grain size (several centimetres), high abundance, and an exceptionally high δ11B value. The formation of tourmaline at the contact between mafic or felsic HP blocks and their ultramafic matrix involved fluids released during dehydration reactions in the subducting slab. It forms a heavy-boron reservoir in hybrid rocks overlying the subducting slab, and may, thus, have a significant impact on the geochemical cycle of B and its isotopes in subduction zone

The crystalline units of the High Himalayas in the Lahul-Zanskar region (northwest India): metamorphic-tectonic history and geochronology of the collided and imbricated Indian plate

In the High Himalayan belt of northwest India, crustal thickening linked to Palaeogene collision between India and Eurasia has led to the formation of two main crystalline tectonic units separated by the syn-metamorphic Miyar Thrust: the High Himalayan Crystallines sensu stricto (HHC) at the bottom, and the Kade Unit at the top. These units are structurally interposed between the underlying Lesser Himalaya and the very low-grade sediments of the Tibetan nappes. They consist of paragneisses, orthogneisses, minor metabasics and, chiefly in the HHC, leucogranites. The HHC registers: a polyphase metamorphism with two main stages designated as M1 and M2; a metamorphic zonation with high-temperature recrystallization and migmatization at middle structural levels and medium-temperature assemblages at upper and lower levels. In contrast, the Kade Unit underwent a low-temperature metamorphism. Rb-Sr and U-Th-Pb isotope data point to derivation of the orthogneisses from early Palaeozoic granitoids, while the leucogranites formed by anatexis of the HHC rocks and were probably emplaced during Miocene time. Most of the complicated metamorphic setting is related to polyphase tectonic stacking of the HHC with the ‘cooler' Kade Unit and Lesser Himalaya during the Himalayan history. However, a few inconsistencies exist for a purely Himalayan age of some Ml assemblages of the HHC. As regards the crustal-derived leucogranites, the formation of a first generation mixed with quartzo-feldspathic leucosomes was possibly linked to melt-lubricated shear zones which favoured rapid crustal displacements; at upper levels they intruded during stage M2 and the latest movements along the syn-metamorphic Miyar Thrust, but before juxtaposition of the Tibetan nappes along the late- metamorphic Zanskar Faul

Boron isotope ratio (delta B-11) measurements in water framework directive monitoring programs: comparison between double focusing sector field ICP and thermal ionization mass spectrometry

International audienceThe aim of our research was to compare delta B-11 measurements performed with thermal ionization mass spectrometry (TIMS) and sector field-inductively coupled plasma-mass spectrometry (SF-ICP-MS) and evaluate the feasibility of implementing stable isotope methods in European water framework directive (WFD) monitoring programs. The comparison was based on delta B-11 measurements of 192 ground-and surface water samples and 15 leachates of nitrate pollution source materials (organic and mineral fertilisers). The precision of delta B-11 measurements attainable with SF-ICP-MS, 2 sigma= +/- 2.6 parts per thousand; (n = 192), is as expected lower than the precision achieved by TIMS, 2 sigma= +/- 0.3 parts per thousand (n=183). However the ease of use, rapidity and availability of SF-ICP-MS on one hand and the observed variability in delta B-11 in ground-and surface water on the other (from -3.4 to +37 parts per thousand), demonstrates that using SF-ICP-MS as an isotopic screening method would promote the use of isotopic methodology for WFD monitoring. Based on the results of the different case studies it is shown that retrieving precise information on the identification of pollution sources from delta B-11 values requires reaching the best analytical precision and accuracy possible. Hence, the superior precision of TIMS advantages tracing of nitrate pollution sources. However for some cases, e. g. trying to decipher contributions between sources with really distinct delta B-11 signatures (e.g. manure and sewage effluent), SF-ICP-MS results lead to the same conclusions and can therefore be used as a first approachable screening method for the determination of delta B-11 in WFD monitoring programs

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

Boron isotopic composition of olivine-hosted melt inclusions from Gorgona komatiites, Colombia : new evidence supporting wet komatiite origin

Author Posting. © The Author(s), 2011. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Earth and Planetary Science Letters 312 (2011): 201–212, doi:10.1016/j.epsl.2011.09.033.A fundamental question in the genesis of komatiites is whether 30 these rocks originate from partial melting of dry and hot mantle, 400−500°C hotter than typical sources of MORB and OIB magmas, or if they were produced by hydrous melting of the source at much lower temperatures, similar or only moderately higher than those known today. Gorgona Island, Colombia, is a unique place where Phanerozoic komatiites occur and whose origin is directly connected to the formation of the Caribbean Large Igneous Province. The genesis of Gorgona komatiites remains controversial, mostly because of the uncertain origin of volatile components which they appear to contain. These volatiles could equally result from shallow level magma contamination, melting of a “damp” mantle or fluid-induced partial melting of the source due to devolatilization of the ancient subducting plate. We have analyzed boron isotopes of olivine40 hosted melt inclusions from the Gorgona komatiites. These inclusions are characterized by relatively high contents of volatile components and boron (0.2−1.0 wt.% H2O, 0.05−0.08 wt.% S, 0.02−0.03 wt.% Cl, 0.6−2.0 μg/g B), displaying positive anomalies in the overall depleted, primitive mantle (PM) normalized trace element and REE spectra ([La/Sm]n = 0.16−0.35; [H2O/Nb]n = 8−44; [Cl/Nb]n = 27−68; [B/Nb]n = 9-30, assuming 300 μg/g H2O, 8 μg/g Cl and 0.1 μg/g B in PM; Kamenetsky et al., 2010. Composition and temperature of komatiite melts from Gorgona Island constrained from olivine-hosted melt inclusions. Geology 38, 1003–1006). The inclusions range in δ11B values from −11.5 to +15.6 ± 2.2‰ (1 SE), forming two distinct trends in a δ11B vs. B-concentration diagram. Direct assimilation of seawater, seawater-derived components, altered oceanic crust or marine sediments by ascending komatiite magma cannot readily account for the volatile contents and B isotope variations. Alternatively, injection of <3% of a 11B enriched fluid to the mantle source could be a plausible explanation for the δ11B range that also may explain the H2O, Cl and B excess.Financial support to AAG during data acquisition and manuscript preparation was provided by Northeast National Ion Microprobe Facility (Woods Hole Oceanographic Institution, USA) and the Centre de Recherches Pétrographiqueset Géochimiques (France). This research was also supported by the Australian Research Council (Research Fellowship and Discovery grants to VSK). We acknowledge partial support of the Alexander von Humboldt Foundation, Germany (F.W. Bessel Award to VSK and Wolfgang Paul Award to A.V. Sobolev who provided access to the electron microprobe at the Max Planck Institute, Mainz, Germany

Serpentinization in the trench-outer rise region offshore of Nicaragua: constraints from seismic refraction and wide-angle data

Recent seismic evidence suggested that most oceanic plate hydration is associated with trench-outer rise faulting prior to subduction. Hydration at trenches may have a significant impact on the subduction zone water cycle. Previous seismic experiments conducted to the northwest of Nicoya Peninsula, Northern Costa Rica, have shown that the subducting Cocos lithosphere is pervasively altered, which was interpreted to be due to both hydration (serpentinization) and fracturing of the crustal and upper-mantle rocks. New seismic wide-angle reflection and refraction data were collected along two profiles, running parallel to the Middle American trench axis offshore of central Nicaragua, revealing lateral changes of the seismic properties of the subducting lithosphere. Seismic structure along both profiles is characterized by low velocities both in the crust and upper mantle. Velocities in the uppermost mantle are found to be in the range 7.3–7.5 km s−1; thus are 8–10 per cent lower than velocities typical for unaltered peridotites and hence confirm the assumption that serpentinization is a common process at the trench-outer rise area offshore of Nicaragua. In addition, a prominent velocity anomaly occurred within the crust beneath two seamounts. Here, velocity reduction may indicate increased porosity and perhaps permeability, supporting the idea that seamounts serve as sites for water percolation and circulation

The effect of subduction on the sulphur, carbon and redox budget of lithospheric mantle

Subduction of hydrated lithospheric mantle introduces H O, ferric iron, oxidized carbon and sulphur to the subduction zone system. The fate of these components is poorly known, but is intimately linked to the global geochemical cycles of iron, carbon and sulphur, the genesis of arc-related ore deposits, the temporal evolution of mantle redox state and subduction-related earthquakes and magmatism. thermocalc is used to provide first-order constraints on the effect of subduction zone metamorphism on metamorphic redistribution of iron, carbon, sulphur and water in ultramafic rocks via construction of P−T and T-X(O) pseudosections with open system calculation of the effect of fluid loss. The calculations replicate observed mineral assemblages in high-P to low-T ultramafic rocks at P−T conditions consistent with those suggested by other workers. The results are consistent with open system fluid loss without significant fluid infiltration. Water loss is complete by 850 C, the corresponding depth of fluid loss being consistent with that inferred for earthquakes in subducting slabs. Losses of carbon and sulphur are relatively minor, at around 5 GPa, below the depths of the source zone for arc volcanoes.Oxygen activity for rocks in closed systems that evolve with a fixed redox budget is calculated to change from ΔFMQ −1 at 350 C to over ΔFMQ +3 at 850 C. This result emphasizes the need to consider redox budget as well as oxygen activity when the results of experiments performed at fixed oxygen activity relative to some buffer are interpreted in the context of natural systems. In open systems, devolatilization is calculated to increase the redox budget and oxygen activity of the residue via loss of methane and H S at the brucite-out and serpentine-out reactions respectively. No fluid-induced mechanism for oxidation of sub-arc mantle by transfer of redox budget from hydrated ultramafic lithologies to the overlying sub-arc mantle was identified, although further thermodynamic data on fluid species such as S are required to confirm this