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Abstract During the subduction of an oceanic plate, fluids are released from metabasaltic crust, metasediment, and serpentinite under high‐pressure/low‐temperature conditions. Although some fluids may eventually leave the slab, some participate in metamorphic reactions within the slab during subduction and exhumation. To identify fluid sources and other controls influencing mineral composition, we report the in situ‐measured δ¹⁸O of lawsonite and garnet in blueschist‐ to eclogite‐facies rocks from 10 subduction zones that represent various field settings, including mélanges, structurally coherent terranes, and an eclogite xenolith derived from a subducted plate. Lawsonite records distinct δ¹⁸O depending on the host rock type and other rock types that were fluid sources during lawsonite growth. In general, lawsonite in metabasalt (7.6 ± 0.2–14.8 ± 1.1‰) is isotopically lighter than in metasediment (20.6 ± 1.4–24.1 ± 1.3‰) but heavier than in metagabbro (4.0 ± 0.4–7.9 ± 0.3‰). The extent of δ¹⁸O fractionation was evaluated for lawsonite–fluid and lawsonite–garnet pairs as a function of temperature (T). Results demonstrate that variations of >1.7‰ in lawsonite and >0.9‰ in garnet are not related to changingT. More likely, the relative contributions of fluids derived from isotopically heavier lithologies (e.g., sediments) versus lighter lithologies (e.g., ultramafic rocks) are the major control. Monte Carlo simulations were performed to investigate the sources of metasomatic fluids and the water/rock ratio that formed lawsonite‐bearing metasomatite. Results indicate that δ¹⁸O_Lwsand δ¹⁸O_Grtrecord interactions with fluids sourced from diverse lithologies (sediment, serpentinite), further supporting that δ¹⁸O_Lwsis a useful indicator of subduction fluid‐rock interactions. 

Abstract Owing to the importance of serpentinites for planetary geochemical and geodynamic processes, there has been much work discerning the origins of their parent rocks, including distinguishing between serpentinites derived from a subducting plate versus overlying mantle in exhumed subduction complexes. The island of New Caledonia (SW Pacific Ocean) provides a rare window into Cenozoic Pacific subduction processes. The island is unique in exposing both an exceptionally preserved high‐pressure, low‐temperature subduction complex and one of the largest supra‐subduction zone ophiolites in the world. Previous studies disagree on the origin of serpentinites in the subduction complex. In this study, we analyze 23 serpentinites from this complex for whole‐rock major and trace element geochemistry and stable isotope (δD, δ¹⁸O) compositions. Our data reveal two distinct groups of serpentinites: Group I samples in the northern portion of the complex are pervasively serpentinized, and exhibit enriched heavy rare earth element (REE) compositions and δ¹⁸O values between +6.7‰ and +10.2‰. In contrast, Group II serpentinites in the south preserve relict orthopyroxene and olivine, and show depleted trace element compositions and comparatively lower δ¹⁸O values between +5.1‰ and +8.0‰. We interpret Group I serpentinites to derive from downgoing plate mantle, whereas Group II serpentinites derive from overlying mantle wedge, exhibiting remarkable similarity to the REE geochemistry of the structurally overlying New Caledonia ophiolite. Our results establish the subduction complex in New Caledonia as an unusual natural record of the entrainment and exhumation of mantle from both the overlying mantle wedge and the downgoing plate in an oceanic subduction zone. 

Abstract. The hydrous Ca–Al silicates lawsonite and epidote group minerals (EGMs) are key phases in subduction-zone H2O and element cycling. In high-pressure–low-temperature metamorphic rocks, Fe in both minerals is typically assumed to be entirely Fe3+, which substitutes for Al in octahedral sites as a major component in most EGMs and as a minor component in lawsonite and zoisite. New Fe micro-X-ray absorption near-edge spectroscopy (μ-XANES) analyses show substantial Fe2+ in lawsonite in blueschist from New Caledonia and zoisite from an unknown locality. Analysed Fe-rich EGMs (epidote, clinozoisite) contain primarily Fe3+. Lawsonite and some EGMs in subducted oceanic crust may contain more Fe2+ than is currently known, with possible implications for understanding subduction redox processes and conditions and why they vary in different subduction zones. 

Abstract Lawsonite is a major host mineral of trace elements (TEs; e.g. REE, Sr, Pb, U, Th) and H2O in various rock types (metabasite, metasediment, metasomatite) over a wide range of depths in subduction zones. Consequently, the composition of lawsonite is a useful archive to track chemical exchanges that occurred during subduction and/or exhumation, as recorded in high-pressure/low-temperature (HP/LT) terranes. This study provides an extensive dataset of major element and TE compositions of lawsonite in HP/LT rocks from two mélanges (Franciscan/USA; Rio San Juan/Dominican Republic), two structurally coherent terranes (Tavşanlı/Turkey; Alpine Corsica/France), and the eclogite blocks of the Pinchi Lake/Canada complex. Bulk major and TE compositions were also determined for lawsonite-bearing host rocks to understand petrogenesis and assess compositional evolution. Most analyzed mélange and coherent-terrane metabasalts have normal mid-ocean ridge/back-arc basin basalt signatures and they preserve compositional evidence supporting interactions with (meta)sediment ± metagabbro/serpentinite (e.g. LILE/LREE enrichments; Ni/Cr enrichments). Most lawsonite grains analyzed are compositionally zoned in transition-metal elements (Fe, Ti, Cr), other TEs (e.g. Sr, Pb), and/or REE, with some grains showing compositional variations that correlate with zoning patterns (e.g. Ti-sector zoning, core-to-rim zoning in Fe, Cr-oscillatory zoning). Our results suggest that compositional variations in lawsonite formed in response to crystallographic control (in Ti-sector zoning), fluid–host rock interactions, modal changes in minerals, and/or element fractionation with coexisting minerals that compete for TEs (e.g. epidote, titanite). The Cr/V and Sr/Pb ratios of lawsonite are useful to track the compositional influence of serpentinite/metagabbro (high Cr/V) and quartz-rich (meta)sediment (low Sr/Pb). Therefore, lawsonite trace and rare earth element compositions effectively record element redistribution driven by metamorphic reactions and fluid–rock interactions that occurred in subduction systems. 

Recycling is not just for plastic. Did you know that the Earth recycles? Recycling happens because the outer part of the planet is made up of large moving pieces of rock. Some of these pieces, called tectonic plates, sink deep down into the Earth. The deeper they go, the more heat and pressure they experience. This causes chemical reactions, including melting of the minerals that make up the rocks. Elements and water trapped inside the melting minerals are released and erupt from volcanoes, returning to the surface. The Earth has recycled! In this article, we present new research on a mineral called lawsonite. Lawsonite only forms in plates that dive into the Earth. Lawsonite has returned to the Earth’s surface in a few rare places where we can collect and analyze it. The composition of elements inside the lawsonite mineral help us understand the deep part of the Earth recycling system.