Olivine from Reykjanes ridge and Iceland tholeiites, and its significance to the two-mantle source model

Abstract Experimental data from the system CaO-MgO-Na 2 O-Al 2 O 3 -SiO 2 and from the system CaO-MgO-FeO-Al 2 O 3 -SiO 2 are used to show the nature of the changes in composition, with temperature and with pressure, of liquids in equilibrium with augite, plagioclase, and olivine as MgO in the system CaO-MgO-Al 2 O 3 -SiO 2 is partially replaced by FeO and as Na 2 O replaces CaO. As differentiation of tholeiitic basalts proceeds, Fe/Mg increases, Na/Ca increases, and normative hypersthene increases and these effects alter the solubilities, and hence the proportions of augite, plagioclase, and olivine which co-precipitate. In particular olivine becomes more soluble (less is precipitated) as Fe/Mg increases; plagioclase becomes more soluble but augite less soluble as Na/(Na + Ca) increases; augite also becomes less soluble as normative hypersthene increases, and as pressure is reduced during ascent. Experimental data from remelted ocean tholeiites encounter the same equilibrium and are presented and compared with the data from synthetic systems. Some natural examples of daughter liquids related to parents by crystallization of augite, plagioclase, olivine, are combined with the experimental data and with some model calculations to demonstrate that only a very limited range of proportions of augite : plagioclase: olivine (approximately 30 : 50 : 15 to 20 : 60: 20) produces daughter liquids which lie on the major element variation of the tholeiitic basalt series. Other proportions lead to daughter liquids which are not basalts. In the light of these restrictions, several recent publications are reinterpreted as examples of fractionation of augite, plagioclase, and olivine, rather than examples of partial melting. The recognition of the small effect that massive (50 to 83%) crystallization has on basaltic chemistry by contrast with the large effect that small accumulations of phenocrysts can have is particularly emphasized in this reinterpretation. Comparisons and possible relationships are suggested between some low-K 2 O, low-TiO 2 tholeiites; some calcic-, aphyric-, dykes of some tholeiitic provinces; some chilled margins of some layered intrusions; some basalts from Iceland, and some basalts from the ocean ridges.

10.1180/minmag.1983.047.343.06

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Citations (26)

Petrological and trace element geochemical features of the Okete Volcanics, western North Island, New Zealand

Contributions to Mineralogy and Petrology (1984)

R. M. Briggs Gordon G. Goleš

Ultramafic rock

Fractional crystallization (geology)

Xenolith

Peridotite

Alkali basalt

Incompatible element