Makoto Miura

Rare nickel hydroxide-hydroxyl carbonate, theophrastite (Ni(OH)₂)-zaratite (Ni₃(CO₃)(OH)₄·4H₂O) aggregates were found from a partially serpentinized dunite from Fujiwara, the Sanbagawa metamorphic belt of high-pressure intermediate type, Japan. The dunite was regionally metamorphosed within the Sanbagawa subduction complex of Cretaceous age. The theophrastite-zaratite aggregate from Fujiwara most typically occurs in association with nickel sulfides, which form a composite grain with awaruite and magnetite within an antigorite-rich part of the rock. The theophraste-zaratite formed possibly together with millerite (NiS) from heazlewoodite (Ni₃S₂). This represents a partial desulfurization of heazlewoodite, which contains or interlocks with laths of antigorite, suggesting their cogenesis. The desulfurization occurred at an early stage of, or during, exhumation of the subduction complex toward the surface, where sulfur was oxidized and removed as sulfate ions. Serpentinization of olivine has not been associated with the formation of theophrastite-zaratite, and an oxidized condition has been kept at this post-serpentinization stage. The sulfate ions liberated in part precipitated anhydrite where calcium was available in the surrounding rocks. This shows one of the shallow migration pathways of sulfur in the subduction zone, especially to the forearc area.

The role of water-rich solutions in the formation of chromitites has been the matter of controversy. We found small chromite concentrations (chromitites) in diopsidites, precipitated from high-temperature hydrothermal fluids, in the mantle to the crust of the Oman ophiolite. Here, we present petrologic characteristics of the hydrothermal chromitites to understand their genesis. In the chromitites, the chromite is associated with uvarovite in the crust and diopside + grossular in the mantle. They are discriminated from the magmatic podiform chromitite by dominance of the Ca-Al silicates in the matrix. The fluids responsible for chromite precipitation are possibly saline, being derived from the seawater circulated into the mantle through the crust. The saline fluids precipitate chromite to form chromite upon decompression and cooling, and transport platinum-group elements (especially Pt and Pd). The fluids obtain Ca and Al from the crustal rocks and Cr from the mantle rocks during circulation. Saline fluids are also supplied from the slab to the mantle wedge, and can metasomatically precipitate chromite and pyroxenes within peridotites. They re-distribute Cr and chromite in peridotites along with circulation of saline fluids in the mantle wedge.

Lithology and petrologic nature of the forearc mantle have been left unclear due to the very limited sampling to date. Here, we present petrological data on a forearc peridotite suite obtained as xenoliths in an alkali basalt dike (7.5 Ma) from the Bankawa area in the Southwest Japan arc for our better understanding of the forearc mantle. The host alkali basalt is of asthenosphere origin, and passed through a slab window with slight chemical modification by the slab-derived component. The Bankawa peridotite suite is comprised of lherzolites, which contain various amounts of secondary phlogopite and were metasomatized to various degrees. The least metasomatized lherzolite exhibits Fo₉₁ of olivine, Cr/(Cr + Al) = 0.3 of chromian spinel, and depletion of middle to light rare-earth elements in clinopyroxene, and is overall similar to an abyssal lherzolite. It had originally formed at the proto-Pacific Ocean and then was trapped at a eastern margin of Eurasian continent by initiation of subduction. The forearc mantle peridotite formed as a residue of proto-arc magma formation is depleted harzburgite as represented by the peridotites obtained from the forearc seafloor, but can be less depleted abyssal peridotite if being devoid of partial melting or reaction with magmas after entrapment.

Ultrahigh-pressure (UHP) chromitites containing UHP minerals such as coesite and diamond have been reported from some ophiolites in Tibet and the Polar Urals. Their nature, i.e., origin, P-T path and abundance, however, are still controversial and left unclear. Here we describe chromitites in the Higashi-akaishi (HA) ultramafic complex in the Cretaceous Sanbagawa metamorphic belt, Japan, which experienced UHP condition (up to 3.8 GPa) at the peak metamorphism via subduction, in order to understand the nature of UHP chromitites. The HA peridotites typically contain garnets and are associated with eclogites, and their associated chromitites are expected to have experienced the UHP metamorphism. The Higashi-akaishi (HA) chromitites show banded to massive structures and are concordant to foliation of the surrounding peridotite. Chromian spinels in the chromitite and surrounding peridotites were sometimes fractured by deformation, and contain various inclusions, i.e., blade- and needle-like diopside lamellae, and minute inclusions of pyroxenes, olivine, and pargasite. The peculiar UHP minerals, such as coesite and diamond, have not been found under the microscope and the Raman spectrometer. Spinels in the HA chromitites show high Cr#s (0.7 to 0.85), and low Ti contents (<0.1 wt %), suggesting a genetic linkage to an arc magma. The HA chromitites share the basic petrographic and chemical features (i.e., diopside lamellae and arc-related spinel chemistry) with the UHP chromitites from Tibet and the Polar Urals. This suggests that some of the characteristics of the UHP chromitite can be obtained by compression, possibly via deep subduction, of low-P chromitite.

The Mersin ophiolite, Turkey, is of typical arc type based on geochemistry of crustal rocks without any signs of mid-ocean ridge (MOR) affinity. We examined its ultramafic rocks to reveal sub-arc mantle processes. Mantle peridotites, poor in clinopyroxene (1 km) in Mersin than in MOR-related ophiolite (mostly < 500 m), and this is one of the features of arc-type ophiolite.

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