This paper presents mineralogical and geochemical data on seafloor massive sulfides (SMS) from the Ashadze-1 hydrothermal field at the Mid-Atlantic Ridge (MAR). The Ashadze-1 deposit is associated with the uplifted lower crust and upper mantle (oceanic core complex, OCC) of the MAR segment characterized by asymmetric mode of accretion. The OCC is represented by deep-seated gabbro-peridotite rocks exhumed on the rift valley slope along the detachment fault, during seafloor spreading. Hydrothermal processes in OCC environments result in different deposit composition and morphology compared to basalt-hosted systems. Abundant chimneys and enrichment in particular metals, including copper, zinc, gold, cobalt and tin are typical for this type of SMS deposit. The Ashadze-1 deposit is considered an example of a hydrothermal system in the initial stage of evolution marked by the young age of the sulfides (<7.2 kyr). The mineralogy of Ashadze-1 reflects primary ore-forming processes unaffected by post formation alteration. We propose a model for the primary ore-forming hydrothermal process in an ultramafic-hosted environment on the modern seafloor.
The Semyenov-2 hydrothermal field located at 13°31′N of the Mid-Atlantic Ridge (MAR) is associated with an oceanic core complex (OCC) and hosted by peridotites and basalts with minor amounts of gabbro and plagiogranites. Seafloor massive sulphides (SMS) are represented by chimneys with zonality, massive sulphides without zonality and sulphide breccia cemented by opal and aragonite. The mean value of Au (20.6 ppm) and Te (40 ppm) is much higher than average for the MAR SMS deposits (3.2 ppm and 8.0 ppm, respectively). Generally, these high concentrations reflect the presence of a wide diversity of Au and Te minerals associated with major mineral paragenesis: primary native gold, melonite (NiTe2) and tellurobismuthite (Bi2Te3) are related to high-temperature chalcopyrite (~350 °C); electrum (AuAg)1, hessite (Ag2Te) and altaite (PbTe) are related to medium- and low-temperature Zn-sulphide and opal assemblages (260–230 °C). Calaverite (AuTe2) and Te-rich “fahlore” Cu12(Sb,As,Te)4S13 are texturally related to the chalcopyrite-bornite-covellite. Enrichment of Au in sulphide breccia with opal and aragonite cement is driven by the re-deposition and the process of hydrothermal reworking of sulphide. The low-temperature fluid mobilizes gold from primary sulphide, along with Au and Te minerals. As a result, the secondary gold re-precipitate in cement of sulphide breccia. An additional contribution of Au enrichment is the presence of aragonite in the Cu-Zn breccia where the maximal Au content (188 ppm) is reached.
The massive sulfide ores of the Pobeda hydrothermal fields are grouped into five main mineral microfacies: (1) isocubanite-pyrite, (2) pyrite-wurtzite-isocubanite, (3) pyrite with minor isocubanite and wurtzite-sphalerite microinclusions, (4) pyrite-rich with framboidal pyrite, and (5) marcasite-pyrite. This sequence reflects the transition from feeder zone facies to seafloor diffuser facies. Spongy, framboidal, and fine-grained pyrite varieties replaced pyrrhotite, greigite, and mackinawite “precursors”. The later coarse and fine banding oscillatory-zoned pyrite and marcasite crystals are overgrown or replaced by unzoned subhedral and euhedral pyrite. In the microfacies range, the amount of isocubanite, wurtzite, unzoned euhedral pyrite decreases versus an increasing portion of framboidal, fine-grained, and spongy pyrite and also marcasite and its colloform and radial varieties. The trace element characteristics of massive sulfides of Pobeda seafloor massive sulfide (SMS) deposit are subdivided into four associations: (1) high temperature—Cu, Se, Te, Bi, Co, and Ni; (2) mid temperature—Zn, As, Sb, and Sn; (3) low temperature—Pb, Sb, Ag, Bi, Au, Tl, and Mn; and (4) seawater—U, V, Mo, and Ni. The high contents of Cu, Co, Se, Bi, Te, and values of Co/Ni ratios decrease in the range from unzoned euhedral pyrite to oscillatory-zoned and framboidal pyrite, as well as to colloform and crystalline marcasite. The trend of Co/Ni values indicates a change from hydrothermal to hydrothermal-diagenetic crystallization of the pyrite. The concentrations of Zn, As, Sb, Pb, Ag, and Tl, as commonly observed in pyrite formed from mid- and low-temperature fluids, decline with increasing crystal size of pyrite and marcasite. Coarse oscillatory-zoned pyrite crystals contain elevated Mn compared to unzoned euhedral varieties. Framboidal pyrite hosts maximum concentrations of Mo, U, and V probably derived from ocean water mixed with hydrothermal fluids. In the Pobeda SMS deposit, the position of microfacies changes from the black smoker feeder zone at the base of the ore body, to seafloor marcasite-pyrite from diffuser fragments in sulfide breccias. We suggest that the temperatures of mineralization decreased in the same direction and determined the zonal character of deposit.
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