Reaction between mid‐ocean ridge basalt (MORB) and crystal mush in the lower oceanic crust has been invoked to explain chemical variations of both MORB and minerals in the lower oceanic crust. Nonetheless, such reactions have been little studied experimentally. We conducted experiments to investigate the mechanisms and chemical consequences of melt‐mush interaction by reacting molten MORB with troctolite at 0.5 GPa. Isothermal experiments demonstrate that melt infiltrates into troctolite with dissolution of plagioclase and olivine. The reacted melts have higher MgO and Al2O3and lower TiO2and Na2O contents and crystallize more primitive olivine and plagioclase compared to those crystallized from the unreacted melts, suggesting melt‐mush reaction could result in the formation of high‐Al basalt. The melt compositional variations induced by reaction also significantly affect the calculated pressures for MORB fractionation, indicating that major element‐based barometers for MORB fractionation can only be used reliably if reaction can be ruled out. After reaction, the troctolite contains olivine with plagioclase inclusions and poikilitic clinopyroxene with partially resorbed olivine and plagioclase chadacrysts, indicating that melt‐mush interaction occurs through dissolution‐reprecipitation mechanisms. Clinopyroxene has high Mg# (>83) and elevated Na2O and TiO2contents, and olivine has different Fo versus Ni correlations from fractional crystallization models, which provide testable parameters for the effect of melt‐mush reaction in the rock record. By comparison with samples from lower oceanic crust and layered intrusions, we propose that melt‐mush reaction plays an important role during magma transport in the crystal mush in both oceanic and continental magma systems.
Oceanic Zircon Records Extreme Fractional Crystallization of MORB to Rhyolite on the Alarcon Rise Mid-Ocean Ridge
Abstract The first known occurrence of rhyolite along the submarine segments of the mid-ocean ridge (MOR) system was discovered on Alarcon Rise, the northernmost segment of the East Pacific Rise (EPR), by the Monterey Bay Aquarium Research Institute in 2012. Zircon trace element and Hf and O isotope patterns indicate that the rhyolite formed by extreme crystal fractionation of primary mid-ocean ridge basalt (MORB) sourced from normal to enriched MOR mantle with little to no addition of continental lithosphere or hydrated oceanic crust. A large range in zircon ɛHf spanning 11 ɛ units is comparable to the range of whole rock ɛHf from the entire EPR. This variability is comparable to continental granitoids that develop over long periods of time from multiple sources. Zircon geochronology from Alarcon Rise suggests that at least 20 kyr was needed for rhyolite petrogenesis. Grain-scale textural discontinuities and trace element trends from zircon cores and rims are consistent with crystal fractionation from a MORB magma with possible perturbations associated with mixing or replenishment events. Comparison of whole rock and zircon oxygen isotopes with modeled fractionation and zircon-melt patterns suggests that, after they formed, rhyolite magmas entrained hydrated mafic crust from conduit walls during ascent and/or were hydrated by seawater in the vent during eruption. These data do not support a model where rhyolites formed directly from partial melts of hydrated oceanic crust or do they require assimilation of such crust during fractional crystallization, both models being commonly invoked for the formation of oceanic plagiogranites and dacites. A spatial association of highly evolved lavas (rhyolites) with an increased number of fault scarps on the northern Alarcon Rise might suggest that low magma flux for ~20 kyr facilitated extended magma residence necessary to generate rhyolite from MORB.
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- Award ID(s):
- 2004618
- NSF-PAR ID:
- 10397169
- Date Published:
- Journal Name:
- Journal of Petrology
- Volume:
- 63
- Issue:
- 6
- ISSN:
- 0022-3530
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1093/petrology/egac040
