No abstract

On Earth, most of the critical processes happen at the frontiers between envelopes and especially at the Moho between the mantle and the crust. Beneath oceanic spreading centres, the dunitic transition zone (DTZ) appears as a major interface between the upwelling and partially molten peridotitic mantle and the accreting gabbroic lower crust. Better constraints on the processes taking part in the DTZ allows improved understanding of the interactions between silicate melts and hydrated fluids, which act competitively to generate the petrological Moho. Here we combine mineral and whole rock major and trace element data with a structural approach along three cross-sections up to 300 m thick above the fossil Maqsad mantle diapir (Oman ophiolite) in order to understand the vertical organization of the DTZ with depth. Our results highlight that most of the faults or fractures cross-cutting the DTZ were ridge-related and active at an early, high temperature magmatic stage. Chemical variations along the cross-sections define trends with a characteristic vertical scale of few tens *Manuscript EPSL-D-18-00894R3 Click here to view linked References of meters. There is a clear correlation between the chemical variation pattern and the distribution of fault zones, not only for fluid-mobile elements but also for immobile elements such as REE and HFSE. Faults, despite displaying very limited displacements, enhanced both melt migration and extraction up to the crust and deep hydrothermal fluids introduction down to the Moho level. We propose that these faults are a vector for upwelling melt modification by hybridization, with hydrothermal fluids and/or silicic hydrous melts, and crystallization. Infiltration of these melts or fluids in the country rock governs part of the gradational evolutions recorded in composition of both the olivine matrix and interstitial phases away from faults. Finally, these faults likely control the thermal structure of the mantle-crust transition as evidenced by the spatial distribution of the crystallization products from percolating melts, organizing the transition zone into pure dunites to impregnated dunites horizons. In this context, the DTZ appears as a reactive interface that developed by the combination of three primary processes: tectonics, magmatism and deep, high temperature hydrothermal circulations. Accordingly, these features fundamentally contribute to the variable petrological and geochemical organization of the DTZ and possibly of the lower crust below oceanic spreading centers, and may be a clue to interpret part the heterogeneity observed in MORB signatures worldwide.

The Maqsad area in the Oman ophiolite exposes a >300 m thick dunitic mantle-crust transition zone (DTZ) that developed above a mantle diapir. The Maqsad DTZ is primarily f "p " w h scattered chromite and chromite seams) and " p g " which exhibit a significant lithological variability, including various kinds of clinopyroxene-, plagioclase-, orthopyroxene-, amphibole (hornblende/pargasite)bearing dunites. These minerals are interstitial between olivine grains and their variable abundance and distribution suggest that they crystallized from a percolating melt. Generally studied through in-situ mineral characterization, the whole rock composition of dunites is poorly documented. This study reports on whole rock and minerals major and trace element *Manuscript contents on 79 pure to variably impregnated dunites collected systematically along cross sections from the base to the top of the DTZ. In spite of its high degree of depletion, the olivine matrix is selectively enriched in the most incompatible trace elements such as LREE, HFSE, Th, U, Rb and Ba. These data support the view that this enrichment has been acquired early in the magmatic evolution of the DTZ, during the dunitization process itself. The dissolution of orthopyroxene from mantle harzburgites enhanced by the involvement of hydrothermal fluids produced low amounts of melts enriched in silica and in some trace elements that re-equilibrated with the olivine matrix. This pristine signature of the DTZ dunite was eventually variably altered by percolation of melts with a Mid-Ocean Ridge Basalt (MORB) affinity but displaying a wide spectrum of composition attributable to evolution by fractional crystallization and hybridization with the silica enriched, hydrated melts. The olivine matrix has been partially or fully re-equilibrated with these melts, smoothing the early strong concave-upward REE pattern in dunite. The chemical variability in the interstitial minerals bears witness of the percolation of MORB, issued from the mantle decompression melting, variably hybridized with melt batches produced within the DTZ by melt-rock reaction and poorly homogenized before reaching the lower crust. Our results lead to the conclusion that pure and impregnated dunites are end-members that recorded different stages of the same initial igneous processes: pure dunites are residues left after extraction of a percolating melt while impregnated dunites correspond to a stage frozen before complete melt extraction. Therefore dunites trace elements contents allow deciphering the multi-stage processes that led to their formation at the mantle-crust transition zone. Keywords Oman ophiolite; dunitic mantle-crust transition zone; trace elements; melt-rock reactions; melt percolation; refertilization 1995a; Kelemen et al., 1997b). In this way, the DTZ appears to be a reactive interface where melts are focused, transformed and potentially accumulated, then distributed beneath the midocean ridge. Crystallization associated to melt migration through the mantle-crust transition zone accou...

The evolution of the seawater oxygen isotopic composition (δ18O) through geological time remains controversial. Yet, the past δ18Oseawater is key to assess past seawater temperatures, providing insights into past climate change and life evolution. Here we provide a new and unprecedentedly precise δ18O value of −1.33 ± 0.98‰ for the Neoproterozoic bottom seawater supporting a constant oxygen isotope composition through time. We demonstrate that the Aït Ahmane ultramafic unit of the ca. 760 Ma Bou Azzer ophiolite (Morocco) host a fossil black smoker-type hydrothermal system. In this system we analyzed an untapped archive for the ocean oxygen isotopic composition consisting in pure magnetite veins directly precipitated from a Neoproterozoic seawater-derived fluid. Our results suggest that, while δ18Oseawater and submarine hydrothermal processes were likely similar to present day, Neoproterozoic oceans were 15–30 °C warmer on the eve of the Sturtian glaciation and the major life diversification that followed.

The Moroccan Anti-Atlas orogenic belt encloses several Precambrian inliers comprising two major Neoproterozoic ophiolitic complexes: the Sirwa and Bou Azzer ophiolites. These ophiolites expose crustal and mantle units, thrusting over fragments of a long-lived intra-oceanic arc system. We present a detailed geochronological and petrogeochemical study of three mafic/ultramafic units of these two ophiolites: the Khzama sequence (Sirwa ophiolite) and the Northern and Southern Aït Ahmane sequences (Bou Azzer ophiolite). The crystallization of layered metagabbros from the Bou Azzer ophiolite (North Aït Ahmane sequence) has been dated here at 759 ± 2 Ma (U-Pb on zircons). This new age for the Bou Azzer ophiolite is similar to the formation of the Sirwa ophiolite (762 Ma) and suggests that both units formed during the same spreading event. Metabasalts of the three units show tholeiitic signature but with variable subduction-related imprints marked by LILE enrichments, HFSE depletions and variable Ti contents, similar to modern back-arc basin basalts (BABB). Their back-arc origin is also supported by the geochemical signature of ultramafic units showing very low contents in major and trace incompatible elements (Al 2 O 3 : 0.12-1.53 wt%, Ti: 3.5-64.2 ppm and Nb: 0.004-0.10 ppm), attesting of a highly refractory protolith. This is in agreement with the high Cr# (0.44-0.81) and low to intermediate Mg# (0.25-0.73) of their constitutive Cr-spinels. Dynamic melting models suggest that these serpentinites experienced intense and polyphased hydrous melting events, strongly influenced by supra-subduction zone SSZ-fluid influx and subduction-related melt percolation. Being particularly affected by these SSZ-melt/rock interactions and closer to arc units to the south, the Sirwa ophiolite and the South Aït Ahmane unit of the Bou Azzer ophiolite likely represent an early stage of the arc-back-arc system, which has been more influenced by the magmatic products of the arc activity compared to the North Aït Ahmane unit of the Bou Azzer ophiolite.

We present an integrated study combining detailed field, geochronological and geochemical data of a Neoproterozoic intra-oceanic arc systems exposed in the Pan-African belt of the Moroccan Anti-Atlas. The arc rock units exposed in Bou Azzer and Sirwa inliers consist of a tectonic patchwork of back-arc ophiolitic sequences to the north thrusted onto accreted arc complexes to the south. Arc complexes are composed of amphibolite, granodioritic and granitic gneisses intruded by various undeformed hydrous ultramafic (hornblendite), mafic (hornblende-gabbro, diorite) and felsic (granodiorite, tonalite, granite) arc lithologies. We show that these complexes are remnants of a long-lived (120 Myr) Neoproterozoic oceanic arc, punctuated by three successive magmatic episodes (760-730 Ma, 710-690 Ma, 660-640 Ma respectively) interspersed with periods of magmatic quiescence. The typical geochemical arc signature and positive ƐNd t values for the igneous rocks emplaced during each magmatic episode (medians at +7.1, +5.4 and +5.7, from older to younger) attest that their parental magmas derived from a depleted mantle source without substantial assimilation by the WAC older crustal basement. Trace-element geochemistry, i.e. Sr/Y, La/Yb, of intermediate to felsic arc rocks produced during each magmatic pulse suggests that the arc crust was thickened (> 30-35 km) over a short time period between the first and second magmatic episodes (730-710 Ma) which coincides with an important regional shortening event. Soft-docking of the oceanic arc on a buoyant transitional margin is invoked to explain tectonic inversion in overriding plate, leading to shortening and related thickening of the arc crust. Concomitant magmatic shutdown resulting from a reorganization of subduction dynamics (i.e. change in slab geometry, flip in subduction polarity). A non-tectonic critical thickening of the arc crust is invoked to explain the second magmatic shutdown (680-660 Ma), by freezing the subarc mantle influx. This lull period is followed by a third magmatic episode which is likely triggered by delamination of the dense lower crust and reactivation of subarc mantle flow. This is supported by the bimodal chemical signature of evolved magmatic products, suggesting two distinct sources partial melts from the foundered lower crust and new magmatic products which differentiated from a post-delamination thinned crust.

The establishment of the Antarctic Circumpolar Current (ACC) is one of the most important events for both global oceanic circulation and climate of the Cenozoic. The onset of this major current hinges on the opening of two major oceanic passages, the Drake Passage and the Tasmanian gateways that connect Pacific, Atlantic and Indian oceans allowing a modern-like thermohaline circulation. For decades, the ACC onset has been considered as the trigger of the Oligocene glaciation at 33.7 Ma, which marks the beginning of the modern icehouse climate. Today, this scenario is debated. The main obstacle to evaluate the ACC influence on the Oligocene glaciation remains the ill-constrained timing of the Drake Passage gateway opening. Here, we analyse the geochemical composition and Sr isotope ratio of dated planktonic and benthic foraminifera from two IODP and ODP legs in the Southern Atlantic and Pacific oceans (SAO and PO, respectively) to assess the variability of seawater masses' chemical composition through time and to better constrain the timing of the Drake Passage gateway opening along the Eocene-Oligocene interval. These results, based on seawater paleo temperature (Mg/Ca molar ratios), redox (Ce/Ce* anomaly) and provenance ( 87 Sr/ 86 Sr) proxies, highlight a gradual seawater mass mixing between the SAO and PO from 31 Ma to 26 Ma. Combined with a reconsideration of the fossil fish teeth Neodymium isotope records, these geochemical tracers evidencing the SAO-PO interconnection depicts the Drake Passage gateway opening and deepening during this 31-26 Ma interval and thus, the timing of the ACC onset. Hence, antecedence of the Oligocene glaciation onset (at 33.7 Ma) relative to the ACC onset (31-26 Ma) implies that the ACC did not trigger the Oligocene glaciation and that the role of atmospheric pCO2 should be further considered.

No abstract