New crystallization temperatures for four eruptions from the Northern Volcanic Zone of Iceland are determined using olivine-spinel aluminum exchange thermometry. Differences in the olivine crystallization temperatures between these eruptions are consistent with variable extents of cooling during fractional crystallization. However, the crystallization temperatures for Iceland are systematically offset to higher temperatures than equivalent olivine-spinel aluminum exchange crystallization temperatures published for MORB, an effect that cannot be explained by fractional crystallization. The highest observed crystallization temperature in Iceland is 1399 6 208C. In order to convert crystallization temperatures to mantle potential temperature, we developed a model of multilithology mantle melting that tracks the thermal evolution of the mantle during isentropic decompression melting. With this model, we explore the controls on the temperature at which primary melts begin to crystallize, as a function of source composition and the depth from which the magmas are derived. Large differences (2008C) in crystallization temperature can be generated by variations in mantle lithology, a magma's inferred depth of origin, and its thermal history. Combining this model with independent constraints on the magma volume flux and the effect of lithological heterogeneity on melt production, restricted regions of potential temperature-lithology space can be identified as consistent with the observed crystallization temperatures. Mantle potential temperature is constrained to be 1480
The 2018 lower East Rift Zone (LERZ) eruption and the accompanying collapse of the summit caldera marked the most destructive episode of activity at Kı̄lauea Volcano in the last 200 years. The eruption was extremely well‐monitored, with extensive real‐time lava sampling as well as continuous geodetic data capturing the caldera collapse. This multiparameter data set provides an exceptional opportunity to determine the reservoir geometry and magma transport paths supplying Kı̄lauea’s LERZ. The forsterite contents of olivine crystals, together with the degree of major element disequilibrium with carrier melts, indicates that two distinct crystal populations were erupted from Fissure 8 (termed high‐ and low‐Fo). Melt inclusion entrapment pressures reveal that low‐Fo olivines (close to equilibrium with their carrier melts) crystallized within the Halema’uma’u reservoir (∼2‐km depth), while many high‐Fo olivines (>Fo81.5; far from equilibrium with their carrier melts) crystallized within the South Caldera reservoir (∼3–5‐km depth). Melt inclusions in high‐Fo olivines experienced extensive post‐entrapment crystallization following their incorporation into cooler, more evolved melts. This favored the growth of a CO2‐rich vapor bubble, containing up to 99% of the total melt inclusion CO2 budget (median = 93%). If this CO2‐rich bubble is not accounted for, entrapment depths are significantly underestimated. Conversely, reconstructions using equation of state methods rather than direct measurements of vapor bubbles overestimate entrapment depths. Overall, we show that direct measurements of melts and vapor bubbles by secondary‐ion mass spectrometry and Raman spectroscopy, combined with a suitable H2O‐CO2 solubility model, is a powerful tool to identify the magma storage reservoirs supplying volcanic eruptions.
Understanding the solubility and degassing of volatiles in silicate melts is a crucial component of modeling volcanic systems. As dissolved components, volatiles (primarily 2 H E O and 2 CO E) affect magma viscosity, rheology, and crystal growth. In addition, due to the strong dependence of volatile solubility on pressure, measured volatile concentrations in preserved high-pressure melts (i.e., melt inclusions: liquid magma trapped within crystals at high pressure, then brought to the surface during an eruption) can be used to determine preeruptive magmatic storage pressures, and thus depths. Importantly, volatile exsolution-driven overpressure of a magmatic system is likely the trigger of many explosive volcanic eruptions (Blake, 1984; Stock IACOVINO ET AL.
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