Abstract

Basaltic crystal cargoes often preserve records of mantle-derived chemical variability that have been erased from their carrier liquids by magma mixing. However, the consequences of mixing between similarly primitive but otherwise chemically variable magmas remain poorly understood despite ubiquitous evidence of chemical variability in primary melt compositions and mixing-induced disequilibrium within erupted crystal cargoes. Here we report observations from magma–magma reaction experiments performed on analogues of primitive Icelandic lavas derived from distinct mantle sources to determine how their crystal cargoes respond to mixing-induced chemical disequilibrium. Chemical variability in our experimental products is controlled dominantly by major element diffusion in the melt that alters phase equilibria and triggers plagioclase resorption within regions that were initially plagioclase saturated. Isothermal mixing between chemically variable basaltic magmas may therefore play important but previously underappreciated roles in creating and modifying crystal cargoes by unlocking plagioclase-rich mushes and driving resorption, (re-)crystallisation and solid-state diffusion.

Highlights

  • Physical mingling is vital for homogenising mantle-derived chemical variability in primitive basalts, diffusion is required for all phases to attain equilibrium

  • In line with dynamic mixing experiments[30,31,32], our magma–magma reaction experiments suggest that chemically variable magmas must be mechanically thinned to filaments no more than a few mm wide for diffusive homogenisation to be achieved within the day-long timescales associated with mixing processes in basaltic plumbing systems[24,25]

  • Chemical variability in olivine-hosted melt inclusions from individual eruptions records the entrapment of variably mixed melts, suggesting that crystallisation and diffusive homogenisation occur over broadly similar timescales[8,15]

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Summary

Introduction

Where error functions could be fitted to our glass composition profiles by assuming that melt viscosity does not vary across experimental products (Supplementary Data 7), estimated effective binary diffusion coefficients are typically within one ln unit of regressions through published datasets that follow Mg#cpx = Mg/(Mg + Fe) on a molar basis] is related to sector zoning[55], a slight difference in mean Mg#cpx between the products of the experiments on the Háleyjabunga and Stapafell analogues (0.835 versus 0.850, respectively) reflects differences in their melt FeO* contents (Fig. 8c).

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