Vicente López Sánchez-Vizcaíno

Enrichment of HFSE in chlorite-harzburgite produced by high-pressure dehydration of antigorite-serpentinite: Implications for subduction magmatism

[1]xa0Depletion of high-field-strength trace elements (HFSE) relative to normal mid-ocean basalts (N-MORB) is the most distinctive geochemical fingerprint of subduction magmatism. Proposed hypotheses advocate that this “subduction” signature is acquired during melting and/or fluid transfer either in the mantle wedge or in the crust of the subducting oceanic plate. Here we provide field-based and geochemical evidence showing that high-pressure dehydration of antigorite-serpentinite produces chlorite-harzburgite relatively enriched in HFSE due to the stabilization of F-OH-Ti-clinohumite intergrowths with prograde olivine. Available experimental data indicate that in hydrated, intermediate to warm subduction zones, clinohumite-olivine intergrowths can be stable in prograde chlorite-harzburgite olivine at subarc depths. In these settings, deserpentinization may act as a source of fluids leaching large-ion lithophile elements (LILE), Pb, and Sr from the overlying crust and sediments on their way up to the mantle wedge. Stabilization of chlorite-harzburgites with clinohumite-olivine intergrowths in the mantle wedge, on the other hand, acts as a sink of HFSE by selectively fractionating them from other incompatible trace elements in fluids emanating from the slab. Resulting arc fluids in equilibrium with wedge chlorite-harzburgite are strongly depleted in HFSE and transfer this depletion to the overlying hot mantle wedge, where subduction magmas are generated.

Retrograde formation of NaCl-scapolite in high pressure metaevaporites from the Cordilleras Béticas (Spain)

AbstractA Permo-Triassic pelite-carbonate rock series (with interacalated metabasitic rocks) in the Cordilleras Béticas, Spain, was metamorphosed during the Alpine metamorphism at high pressures (Pmin near 18 kbar). The rocks show well preserved sedimentary features of evaporites such as pseudomorphs of talc, of kyanite-phengitetalc-biotite, and of quartz after sulfate minerals, and relicts of baryte, anhydrite, NaCl, and KCl, indicating a salt-clay mixture of illite, chlorite, talc, and halite as the original rock. The evaporitic metapelites have a whole rock composition characterized by high Mg/(Mg+Ca) ratios>0.7, variable alkaline and Sr, Ba, contents, but are mostly K2O rich (<8.8 wt%). The F (<2600 ppm), Cl (<3600 ppm), and P2O5 (<0.24 wt%) contents are also high. The pelitic member of this series is a fine grained biotite rock. Kyanite-phengite-talc-biotite aggregates in pseudomorphs developed in the high pressure stage. Albite-rich plagioclase was formed when the rocks crossed the albite stability curve in the early stages of the uplift. Scapolite, rich in NaCl (Ca/(Ca+Na) mol% 24–40) and poor in SO4, with Cl/(Cl+CO3) ratios between 0.6 and 0.8, formed as porphyroblasts, sometimes replacing up to 60% of the rock in a late stage of metamorphism (between 10 and 5 kbar, near 600°C). No reaction with albite is observed, and the scapolite formed from biotite by: n

FTIR and Raman spectroscopy characterization of fluorine-bearing titanian clinohumite in antigorite serpentinite and chlorite harzburgite

begin{gathered} Al - biotite + CaCO_3 + NaCl + SiO_2 hfill = Al - poor biotite + scapolite + MgCO_3 + KCl hfill + MgCl_2 + H_2 O hfill end{gathered}

Metamorphic Record of High-pressure Dehydration of Antigorite Serpentinite to Chlorite Harzburgite in a Subduction Setting (Cerro del Almirez, Nevado–Filábride Complex, Southern Spain)

nnCalculated fluid composition in equilibrium with scapolite indicates varying salt concentrations in the fluid. Distribution of Cl and F in biotite and apatite also indicates varying fluid compositions.

An experimental investigation of antigorite dehydration in natural silica-enriched serpentinite

AbstractnThe Cerro del Almirez massif (Spain) represents a unique fragment of serpentinized oceanic lithosphere that has been first equilibrated in the antigorite stability field (Atg-serpentinites) and then dehydrated into chlorite–olivine–orthopyroxene (Chl-harzburgites) at eclogite facies conditions during subduction. The massif preserves a dehydration front between Atg-serpentinites and Chl-harzburgites. It constitutes a suitable place to study redox changes in serpentinites and the nature of the released fluids during their dehydration. Relative to abyssal serpentinites, Atg-serpentinites display a low Fe3+/FeTotal(BR) (=0.55) and magnetite modal content (=2.8–4.3xa0wt%). Micro-X-ray absorption near-edge structure (μ-XANES) spectroscopy measurements of serpentines at the Fe–K edge show that antigorite has a lower Fe3+/FeTotal ratio (=0.48) than oceanic lizardite/chrysotile assemblages. The onset of Atg-serpentinites dehydration is marked by the crystallization of a Fe3+-rich antigorite (Fe3+/FeTotalxa0=xa00.6–0.75) in equilibrium with secondary olivine and by a decrease in magnetite amount (=1.6–2.2xa0wt%). This suggests a preferential partitioning of Fe3+ into serpentine rather than into olivine. The Atg-breakdown is marked by a decrease in Fe3+/FeTotal(BR) (=0.34–0.41), the crystallization of Fe2+-rich phases and the quasi-disappearance of magnetite (=0.6–1.4xa0wt.%). The observation of Fe3+-rich hematite and ilmenite intergrowths suggests that the O2 released by the crystallization of Fe2+-rich phases could promote hematite crystallization and a subsequent increase in fo2 inside the portion of the subducted mantle. Serpentinite dehydration could thus produce highly oxidized fluids in subduction zones and contribute to the oxidization of the sub-arc mantle wedge.

Tschermak's substitution in antigorite and consequences for phase relations and water liberation in high-grade serpentinites

Titanian clinohumite is an accessory phase found in peridotites, and it can be a key repository of volatile and other trace elements in sub-arc mantle. To characterize spectroscopic variations due to volatile elements in the phase, we have investigated the infrared spectroscopic characteristics of a suite of naturally occurring Ti clinohumite minerals with varying F and Ti concentrations. Samples were ultramafic rocks from Cerro del Almirez, Spain and Cima di Gagnone, Switzerland. The infrared spectra corresponding to OH vibrations showed systematic variation in regard to the abundance of F in Ti clinohumite. In particular, the intensity ratios of infrared absorption spectra at 3,565 and 3,390xa0cm-1 correlated linearly with the abundance of F independently of the crystal orientation. Raman spectra did not corroborate the Fourier transform infrared (FTIR) results. This intensity ratio provides an alternative analytical criterion for the characterization of Ti clinohumite.