E.M. Klein | Geology Reports

USGS2011

Volatile abundances and oxygen isotopes in basaltic to dacitic lavas on mid-ocean ridges: The role of assimilation at spreading centers

Most 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.

Chemical Geology↗

USGS2007

Petrology and geochemistry of primitive lower oceanic crust from Pito Deep: Implications for the accretion of the lower crust at the Southern East Pacific Rise

A suite of samples collected from the uppermost part of the plutonic section of the oceanic crust formed at the southern East Pacific Rise and exposed at the Pito Deep has been examined. These rocks were sampled in situ by ROV and lie beneath a complete upper crustal section providing geological context. This is only the second area (after the Hess Deep) in which a substantial depth into the plutonic complex formed at the East Pacific Rise has been sampled in situ and reveals significant spatial heterogeneity in the plutonic complex. In contrast to the uppermost plutonic rocks at Hess Deep, the rocks studied here are generally primitive with olivine forsterite contents mainly between 85 and 88 and including many troctolites. The melt that the majority of the samples crystallized from was aggregated normal mid-ocean ridge basalt (MORB). Despite this high Mg# clinopyroxene is common despite model predictions that clinopyroxene should not reach the liquidus early during low-pressure crystallization of MORB. Stochastic modeling of melt crystallisation at various levels in the crust suggests that it is unlikely that a significant melt mass crystallized in the deeper crust (for example in sills) because this would lead to more evolved shallow level plutonic rocks. Similar to the upper plutonic section at Hess Deep, and in the Oman ophiolite, many samples show a steeply dipping, axis-parallel, magmatic fabric. This suggests that vertical magmatic flow is an important process in the upper part of the seismic low velocity zone beneath fast-spreading ridges. We suggest that both temporal and spatial (along-axis) variability in the magmatic and hydrothermal systems can explain the differences observed between the Hess Deep and Pito Deep plutonics. ?? Springer-Verlag 2007.

Contributions to Mineralogy and Petrology↗