Abstract
The coexistence of sulfide liquids (or more accurately, FeSO liquids) with silicate liquids in a variety of magma systems is well known, as is the ability of immiscible FeSO liquids to segregate Ni, Cu and platinum-group metals into orebodies. Evidence for association of FeSO liquids with magmas that form mid-ocean ridge basalts (MORB) comes from sulfide globules in basalt glass from Siqueiros Fracture Zone, East Pacific Rise; three fracture zones in the Indian Ocean; Lau Basin; and ∼ 23 previously published oceanic localities. Approximately 40% of the sulfur originally present in magma at Siqueiros Fracture Zone exsolves as a sulfide liquid during fractional crystallization. Virtually all of the Cu, and 20% of the Ni, originally in the magma is extracted by the sulfide liquid. Significant variations in the ability of FeSO liquids to partition Ni Cu exist among MORB and other mafic magmas, such as komatiites and layered mafic intrusions. Nernst partition coefficients (sulfide to silicate melt; D S L ) are 2–3 times higher for Ni in MORB than in komatiite, and ∼ 5 times higher for Cu. Reasons for this variation are not entirely clear, but a possible contributing factor is that FeSO liquids in MORB appear to have a higher oxygen content than those in komatiites. That FeSO liquids associated with MORB magma are oxygen-rich is suggested by low observed values at Siqueiros Fracture Zone for the NiFe exchange coefficient K D3 [1.21−4.56; K D3 = ( Fe Ni ) olivine ( Fe Ni ) sulfide ]. It has been previously shown that natural magmatic FeSO liquids are rich in O 2− [ O ( S + O) is apparently always greater than ∼ 0.49], and that K D3 is inversely correlated with O ( S + O) . K D3-values below ∼ 12 would result from FeSO liquids with O ( S + O) > 0.49 . K D3-value of> 20 would be impossible (values from 12 to 20 would be unlikely) because they would require an FeSO liquid poor in O 2−. This argument for low K D3 in magmas is strengthened by the low K D3-values of MORB, whose globules are inarguably of magmatic origin. K D3 in komatiites is higher than in MORB (indicating a lower oxygen fugacity in komatiite magma) and varies from ∼ 5 to > 20, with values of > 20 coming from highly metamorphosed komatiites. Fleet and MacRae argued on the basis of experimental results that K D3-values of < 20 could not result from equilibration at magmatic temperatures and that orebodies associated with komatiites would have to be of hydrothermal origin. But those experiments were carried out at O ( S + O) = 0 , an unrealistic value for magmatic FeSO liquids. K D3-values in komatiites of > 20 could not have resulted from magmatic processes, but might have come from metamorphism under oxygen-deficient conditions.
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