The metallogeny of Japan can be grouped into four environments: (1) Paleozoic-Mesozoic stratiform Cu and Mn deposits within accretionary complexes, (2) Cretaceous-Paleogene post-accretionary deposits related to felsic magmatism in a continental-margin arc environment, (3) Miocene epigenetic and syngenetic deposits related to felsic magmatism during back-arc opening, and (4) late Miocene-Quaternary volcanogenic deposits in an island-arc environment. Group (1) deposits were a major source of Cu and Mn for the Japanese mining industry, and this style of mineralization is reviewed here. The stratiform Cu and Mn deposits were formed on the sea floor during the late Paleozoic to Mesozoic, and were subsequently accreted to active continental margins mainly in Jurassic to Cretaceous age. The Cu sulfide deposits, termed Besshi type, are classified into two subtypes: the Besshi-subtype deposit is related to basaltic volcanism, probably at a mid-oceanic ridge or rise; the Hitachi subtype is related to bimodal volcanism, probably in a back-arc or continental rift. Most of the Besshisubtype deposits occur in the Sanbagawa metamorphic belt, with some occurrences in weakly metamorphosed Jurassic and Cretaceous accretionary terrains. This subtype is divided into two groups: the sediment-barren group is hosted by basalt-chert sequences; whereas the sedimentcovered group is hosted by basalt-shale sequences. Both subtypes are characterized by S isotope trends similar to those of sea-floor sulfide deposits now forming at mid-oceanic ridges. The Hitachi-subtype deposits occur in late Paleozoic volcanic-sedimentary sequences and lack pelagic sediments. These deposits are characterized by association of sphalerite-and barite-rich ores. The Mn deposits occur mainly in Middle Jurassic to Early Cretaceous accretionary complexes containing abundant chert beds of Triassic to Jurassic age. Their locations are well separated from those of the Cu sulfide deposits. The Mn deposits are divided into two types: the Mn type, hosted by chert, and the Fe-Mn type, sandwiched between chert and basaltic volcanic rocks. The Mn-type ores appear to have deposited on the deep-sea floor further from the site of hydrothermal activity than the Fe-Mn type. Primary Mn precipitates may have been transformed to rhodochrosite and other Mn-minerals during diagenesis. Many of the Mn deposits were significantly metamorphosed during intrusion of Cretaceous granitoids, resulting in a very complex mineralogy.

In Snake Pit massive sulfide fragments and friable, unconsolidated material recovered during ODP Leg 106, isocubanite and pyrite are generally the predominant phases, followed by marcasite, chalcopyrite, sphalerite, and pyrrhotite. Detailed analyses of paragenetic relations of minerals indicate that isocubanite first precipitated together with pyrrhotite. With decreasing temperature, chalcopyrite and sphalerite precipitated, and at the latest stage colloform sphalerite-pyrite (or colloform marcasite) formed. Isocubanite usually has exsolution lamellae of chalcopyrite and less commonly of pyrrhotite.The average bulk chemical composition of the friable, unconsolidated material indicates that it is rich in copper, reflecting the dominance of isocubanite in the specimens, and is characterized by high Co, low Pb, and Ag contents. Sulfur isotope ratios are very uniform, ranging in S 34 S from +1.2 to +2.8%c. The obtained values are apparently low, compared to those for the eastern Pacific sulfide samples, reflecting a smaller contribution of seawater sulfate in the Snake Pit sulfide deposit.

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A sulfide chimney ore sampled from the flank of the active Tiger vent area in the Yonaguni Knoll IV hydrothermal field, south Okinawa trough, consists of anhydrite, pyrite, sphalerite, galena, chalcopyrite and bismuthinite. Electron microprobe analysis indicates that the chalcopyrite contains up to 2.4 wt% Sn, whereas bismuthinite contains up to 1.7 wt% Pt, 0.8 wt% Cu and 0.5 wt% Fe. The Sn-rich chalcopyrite and Pt-Cu-Febearing bismuthinite are the first reported occurrence of such minerals in an active submarine hydrothermal system. The results confirm that Sn enters the chalcopyrite as a solid solution towards stannite by the coupled substitution of Sn , whereas Pt, Cu and Fe enter the bismuthinite structure as a solid solution during rapid nucleation. The fluid inclusions homogenization temperatures in anhydrite (220-310°C) and measured end-member temperature of the vent fluids on-site (325°C) indicate that Sn-bearing chalcopyrite and Pt-Cu-Fe-bearing bismuthinite express the original composition of the minerals that precipitated as metastable phases at a temperature above 300°C. The result observed in this study implies that sulfides in ancient volcanogenic massive sulfide deposits have similar trace element distribution during nucleation but it is remobilised during diagenesis, metamorphism or supergene enrichment processes.

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