Abstract

Current knowledge on the solidus temperature for carbonated eclogites suggests that carbonatitic liquids should not form from a subducted oceanic lithosphere at sub-arc depth. However, the oceanic crust includes a range of gabbroic rocks, altered on rifts and transforms, with large amounts of anorthite-rich plagioclase forming epidote on metamorphism. Epidote disappearance with pressure depends on the normative anorthite content of the bulk composition; we therefore expect that altered gabbros might display a much wider pressure range where epidote persists, potentially affecting the solidus relationships. A set of experimental data up to 4.6 GPa, and 1000 °C, including new syntheses on mafic eclogites with 36.8 % normative anorthite, is discussed to unravel the effect of variable bulk and volatile compositions in model eclogites, enriched in the normative anorthite component (An 37 and An 45). Experiments are performed in piston cylinder and multianvil machines. Garnet, clinopyroxene, and coesite form in all syntheses. Lawsonite was found to persist at 3.7 GPa, 750 °C, with both dolomite and magnesite; at 3.8 GPa, 775–800 °C, fluid-saturated conditions, epidote coexists with kyanite, dolomite, and magnesite. The anhydrous assemblage garnet, omphacite, aragonite, and kyanite is found at 4.2 GPa, 850 °C. At 900 °C, a silicate glass of granitoid composition, a carbonatitic precipitate, and Na-carbonate are observed. Precipitates are interpreted as evidence of hydrous carbonatitic liquids at run conditions; these liquids produced are richer in Ca compared to experimental carbonatites from anhydrous experiments, consistently with the dramatic role of H2O in depressing the solidus temperature for CaCO3. The fluid-absent melting of the assemblage epidote + dolomite, enlarged in its pressure stability for An-rich gabbros, is expected to promote the generation of carbonatitic liquids. The subsolidus breakdown of epidote in the presence of carbonates at depths exceeding 120 km provides a major source of C-O-H volatiles at sub-arc depth. In warm subduction zones, the possibility of extracting carbonatitic liquids from a variety of gabbroic rocks and epidosites offers new scenarios on the metasomatic processes in the lithospheric wedge of subduction zones and a new mechanism for recycling carbon.

Highlights

  • Epidote is a hydroxylated Ca-Al-silicate commonly observed in a variety of high-pressure rocks, from basaltic eclogites, to metagabbros and rodingites of the metamorphosed oceanic crust, to intermediate rock compositions representative of slices of the continental crust involved in high-pressure processes at subduction zones

  • Hydrous phases are absent in all runs on starting material 80-3, with normative anorthite content (An) = 36.8, the stability field of epidote expected to be restricted to approximately 3.5 GPa in this bulk composition

  • The stability field of epidote is maximized in mafic bulk compositions originally enriched in anorthitic plagioclase, and reaches 3.8–4 GPa in phase relations presented here

Read more

Summary

Introduction

Epidote is a hydroxylated Ca-Al-silicate commonly observed in a variety of high-pressure rocks, from basaltic eclogites, to metagabbros and rodingites of the metamorphosed oceanic crust, to intermediate rock compositions representative of slices of the continental crust involved in high-pressure processes at subduction zones. The extent of pressure stability of epidote in eclogites has been proposed to be a function of the normative anorthite content (An) of the bulk composition of the system of interest. Zoisite was found in eclogite assemblages in a MOR basalt composition with normative anorthite content An = 31 % to 3 GPa by Poli et al (2009) and up to at least 4 GPa, 900 °C in a plagioclaserich gabbro, An = 71 % by Wittenberg et al (2003). As the wet solidus for MOR basalts approaches such conditions (Fig. 1), epidote is expected to affect melting of mafic eclogites at pressures largely exceeding the amphibole stability field, down to sub-arc depths. The role and pressure effect of Fe3+ is unexplored and may further expand epidote stability if Fe3+ preferentially partitions in epidote with respect to garnet

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call