Browsing by Author "Ridley, WI"
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Item Open Access Lava geochemistry as a probe into crustal formation at the East Pacific Rise(Oceanography, 2012-03-01) Perfit, MR; Wanless, VD; Ridley, WI; Klein, E; Smith, MC; Goss, AR; Hinds, JS; Kutza, S; Fornari, DJItem Open Access Reconciling geochemical and geophysical observations of magma supply and melt distribution at the 9N overlapping spreading center, East Pacific Rise(Geochemistry, Geophysics, Geosystems, 2012-11-01) Wanless, VD; Perfit, MR; Klein, EM; White, S; Ridley, WIEarly studies of mid-ocean ridge discontinuities, such as transform faults and overlapping spreading centers, suggested a lower magma supply compared to ridge segment centers. This is reflected in bathymetrically deeper ridge axes, decreased hydrothermal activity, and the eruption of more evolved lava compositions. While many signatures of lower magma supply are observed at the 9N overlapping spreading center on the East Pacific Rise, geophysical studies indicate extensive sub-surface melt in the region, suggesting that the present magmatic system is not diminished. Here major and trace element concentrations of erupted lavas are used to better understand magma supply at a large second-order ridge discontinuity. We show that the wide range of lava compositions erupted at the 9N overlapping spreading center is generally consistent with early petrologic models of ridge propagation and require variable degrees of fractional crystallization, extensive magma mixing, and in some instances crustal assimilation. Moderately evolved ferrobasalts and FeTi basalts erupted at the OSC indicate that crustal residence times are long enough for significant crystallization of all magmas within the region, but the presence of dacitic lavas reflects periods of even lower magma supply, where melt replenishment is subordinate to cooling and crystallization. The geophysical observations of extensive melt within the shallow crust are reconciled with the geochemistry of the lavas, if melts are supplied intermittently to the propagating ridge over relatively short timescales. © 2012. American Geophysical Union. All Rights Reserved.Item Open Access Volatile abundances and oxygen isotopes in basaltic to dacitic lavas on mid-ocean ridges: The role of assimilation at spreading centers(Chemical Geology, 2011-08-07) Wanless, VD; Perfit, MR; Ridley, WI; Wallace, PJ; Grimes, CB; Klein, EMMost geochemical variability in MOR basalts is consistent with low- to moderate-pressure fractional crystallization of various mantle-derived parental melts. However, our geochemical data from MOR high-silica glasses, including new volatile and oxygen isotope data, suggest that assimilation of altered crustal material plays a significant role in the petrogenesis of dacites and may be important in the formation of basaltic lavas at MOR in general. MOR high-silica andesites and dacites from diverse areas show remarkably similar major element trends, incompatible trace element enrichments, and isotopic signatures suggesting similar processes control their chemistry. In particular, very high Cl and elevated H2O concentrations and relatively light oxygen isotope ratios (~5.8‰ vs. expected values of ~6.8‰) in fresh dacite glasses can be explained by contamination of magmas from a component of ocean crust altered by hydrothermal fluids. Crystallization of silicate phases and Fe-oxides causes an increase in δ18O in residual magma, but assimilation of material initially altered at high temperatures results in lower δ18O values. The observed geochemical signatures can be explained by extreme fractional crystallization of a MOR basalt parent combined with partial melting and assimilation (AFC) of amphibole-bearing altered oceanic crust. The MOR dacitic lavas do not appear to be simply the extrusive equivalent of oceanic plagiogranites. The combination of partial melting and assimilation produces a distinct geochemical signature that includes higher incompatible trace element abundances and distinct trace element ratios relative to those observed in plagiogranites. © 2011 Elsevier B.V.