Abstract
Primary base metal massive sulphide deposits are formed as a rule in seafloor depressions. Ore formation is preceded by stratification of seawaters into oxiding and reducing zones. Hydrothermal sedimentary pyritic bodies are formed in two stages. During sedimentogenesis, monosulphide iron and non-ferrous thin sediments are accumulated under thermodynamic disequilibrium conditions. During diagenesis, sea-floor sulphide sediments are crystallized as a result of their interaction with pore solutions. The latter, according the thermodynamic data, are characterized by the buffer ratio of sulphur in oxidized and reduced forms. The process of diagenesis results in standard base metal zonation. If pyrite-bearing fluids are characterized by increased total activity of sulphur, then such a zonation is complicated by an additional zonal distribution of sulphides and sulphates. The disappearance of anhydrite at the barite-polymetallic level is due to the spontaneous evolution of the external physical and chemical parameters against a background of temperature decrease and displacement of the invariant barite-calcite-anhydrite equilibrium towards to barite crystallization field.
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© 1986 Springer-Verlag Berlin Heidelberg
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Tvalchrelidze, A.G. (1986). Physico-Chemical Conditions of Base Metal Sulphide Ore Formation. In: Friedrich, G.H., Genkin, A.D., Naldrett, A.J., Ridge, J.D., Sillitoe, R.H., Vokes, F.M. (eds) Geology and Metallogeny of Copper Deposits. Special Publication No. 4 of the Society for Geology Applied to Mineral Deposits, vol 4. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-70902-9_26
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DOI: https://doi.org/10.1007/978-3-642-70902-9_26
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