4.7 Article

Subseafloor sulphide deposit formed by pumice replacement mineralisation

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE RESEARCH
DOI: 10.1038/s41598-021-87050-z

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Funding

  1. Council for Science, Technology and Innovation (CSTI) through its Cross-ministerial Strategic Innovation Promotion Program (SIP) Next-generation technology for ocean resources exploration

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Seafloor massive sulphide (SMS) deposits, future resources of base and precious metals, form through exhalative deposition on the seafloor and subseafloor mineral replacement. Studies of a modern SMS deposit indicate that sulphides initially form as framboidal pyrite aggregates, evolving into colloform and euhedral pyrite, and then being replaced by chalcopyrite, sphalerite and galena. The presence of anhydrite-rich layers within sediment controls precipitation of a sulphide body extending hundreds of meters laterally, impacting global metal cycling.
Seafloor massive sulphide (SMS) deposits, modern analogues of volcanogenic massive sulphide (VMS) deposits on land, represent future resources of base and precious metals. Studies of VMS deposits have proposed two emplacement mechanisms for SMS deposits: exhalative deposition on the seafloor and mineral and void space replacement beneath the seafloor. The details of the latter mechanism are poorly characterised in detail, despite its potentially significant role in global metal cycling throughout Earth's history, because in-situ studies require costly drilling campaigns to sample SMS deposits. Here, we interpret petrographic, geochemical and geophysical data from drill holes in a modern SMS deposit and demonstrate that it formed via subseafloor replacement of pumice. Samples from the sulphide body and overlying sediment at the Hakurei Site, Izena Hole, middle Okinawa Trough indicate that sulphides initially formed as aggregates of framboidal pyrite and matured into colloform and euhedral pyrite, which were replaced by chalcopyrite, sphalerite and galena. The initial framboidal pyrite is closely associated with altered material derived from pumice, and alternating layers of pumiceous and hemipelagic sediments functioned as a factory of sulphide mineralisation. We infer that anhydrite-rich layers within the hemipelagic sediment forced hydrothermal fluids to flow laterally, controlling precipitation of a sulphide body extending hundreds of meters.

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