13 research outputs found

    Pollution from the 2014–15 Bárðarbunga eruption monitored by snow cores from the Vatnajökull glacier, Iceland

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    The chemical composition of Icelandic rain and snow is dominated by marine aerosols, however human and volcanic activity can also affect these compositions. The six month long 2014-15 Bárdarbunga volcanic eruption was the largest in Iceland for more than 200years and it released into the atmosphere an average of 60kt/day SO 2 , 30kt/day CO 2 , 500t/day HCl and 280t/day HF. To study the effect of this eruption on the winter precipitation, snow cores were collected from the Vatnajökull glacier and the highlands northeast of the glacier. In addition to 29 bulk snow cores from that precipitated from September 2014 until March 2015, two cores were sampled in 21 and 44 increments to quantify the spatial and time evolution of the chemical composition of the snow.The pH and chemical compositions of melted snow samples indicate that snow has been affected by the volcanic gases emitted during the Bárdarbunga eruption. The pH of the melted bulk snow cores ranged from 4.41 to 5.64 with an average value of 5.01. This is four times greater H + activity than pure water saturated with the atmospheric CO 2 . The highest concentrations of volatiles in the snow cores were found close to the eruption site as predicted from CALPUFF SO 2 gas dispersion quality model. The anion concentrations (SO 4 , Cl, and F) were higher and the pH was lower compared to equivalent snow samples collected during 1997-2006 from the unpolluted Icelandic Langjökull glacier. Higher SO 4 and Cl concentrations in the snow compared with the unpolluted rainwater of marine origin confirm the addition of a non-seawater SO 4 and Cl. The δ 34 S isotopic composition confirms that the sulphur addition is of volcanic aerosol origin.The chemical evolution of the snow with depth reflects changes in the lava effusion and gas emission rates. Those rates were the highest at the early stage of the eruption. Snow that fell during that time, represented by samples from the deepest part of the snow cores, had the lowest pH and highest concentrations of SO 4 , F, Cl and metals, compared with snow that fell later in the winter. Also the Al concentration, did exceed World Health Organisation drinking water standard of 3.7μmol/kg in the lower part of the snow core closest to the eruption site.Collected snow represents the precipitation that fell during the eruption period. Nevertheless, only minor environmental impacts are evident in the snow due to its interaction with the volcanic aerosol gases. In addition, the microbial communities identified in the snow that fell during the eruption were similar to those found in snow from other parts of the Arctic, confirming an insignificant impact of this eruption on the snow microecology

    Instrumental mass fractionation during sulfur isotope analysis by secondary ion mass spectrometry in natural and synthetic glasses

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    Sulfur isotope ratios are among the most commonly studied isotope systems in geochemistry. While sulfur isotope ratio analyses of materials such as bulk rock samples, gases, and sulfide grains are routinely carried out, in-situ analyses of silicate glasses such as those formed in magmatic systems are relatively scarce in the literature. Despite a number of attempts in recent years to analyse sulfur isotope ratios in volcanic and experimental glasses by secondary ion mass spectrometry (SIMS), the effects of instrumental mass fractionation (IMF) during analysis remain poorly understood. In this study we use more than 600 sulfur isotope analyses of nine different glasses to characterise the matrix effects that arise during sulfur isotope analysis of glasses by SIMS. Samples were characterised for major element composition, sulfur content, and sulfur isotope ratios by independent methods. Our glasses contain between 500 and 3400 ppm sulfur and cover a wide compositional range, including low-silica basanite, rhyolite, and phonolite, allowing us to investigate composition-dependent IMF. We use SIMS in multi-collection mode with a Faraday cup/electron multiplier detector configuration to achieve uncertainty of 0.3‰ to 2‰ (2σ) on measured δ34S. At high sulfur content, the analytical error of our SIMS analyses is similar to that of bulk analytical methods, such as gas-source isotope ratio mass spectrometry. We find IMF causes an offset of −12‰ to +1‰ between bulk sulfur isotope ratios and those measured by SIMS. Instrumental mass fractionation correlates non-linearly with glass sulfur contents and with a multivariate regression model combining glass Al, Na, and K contents. Both ln(S) and Al-Na-K models are capable of predicting IMF with good accuracy: 84% (ln(S)) and 87% (Al-Na-K) of our analyses can be reproduced within 2σ combined analytical uncertainty after a correction for composition-dependent IMF is applied. The process driving IMF is challenging to identify. The non-linear correlation between glass S content and IMF in our dataset resembles previously documented correlation between glass H2O abundance and IMF during D/H ratio analyses by SIMS, and could be attributed to changes in 32S− and 34S− ion yields with changing S content and glass composition. However, a clear correlation between S ion yields and S content cannot be identified in our dataset. We speculate that accumulation of alkalis at the SIMS crater floor may be the principal driving force of composition-dependent IMF. Nonetheless, other currently unknown factors could also influence IMF observed during S isotope ratio analyses of glasses by SIMS. Our results demonstrate that the use of multiple, well-characterised standards with a wide compositional range is required to calibrate SIMS instruments prior to sulfur isotope analyses of unknown silicate glasses. Matrix effects related to glass Al-Na-K contents are of particular importance for felsic systems, where alkali and aluminium contents can vary considerably more than in mafic magmas

    Hydraulically linked reservoirs simultaneously fed the 1975–1984 Krafla Fires eruptions: Insights from petrochemistry

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    The 1975–1984 Krafla Fires in northeast Iceland was the first plate-boundary rifting episode to be tracked using seismic and geodetic monitoring. Geophysical observations from this episode have inspired conceptual models of magma transport during plate spreading, but a lack of complementary petrologic insights has hindered a holistic understanding of the events. To address this knowledge gap, we studied the petrochemistry of all nine Krafla Fires basaltic eruptions. Our large dataset of new whole-rock, matrix glass and mineral analyses from samples collected during or shortly after each eruption reveal a clear compositional bimodality in the erupted magmas that persisted across the episode, with evolved quartz tholeiite (MgO = 5.7–6.4 wt.%) erupted inside Krafla caldera, and more primitive (usually olivine-normative) tholeiite (MgO = 6.4–8.7 wt%) erupted north of the caldera margin. Barometric calculations indicate tapping of these magmas from distinct reservoirs: a primitive lower-crustal reservoir at a most probable depth of ∼14–19 km, and a more evolved, shallower reservoir at a most probable depth of ∼7–9 km beneath the caldera. These reservoirs were tapped simultaneously in several of the nine eruptions, and in three events the two magma types mixed near the northern caldera margin. Varying levels of trace element depletion in the deep-sourced primitive melts reflect incomplete mixing of diverse mantle-derived melts at depth; the most enriched of these melts could be parental to evolved inside-caldera magma via fractional crystallization. Clinopyroxene rims on gabbroic nodules from primitive September 1984 lavas record lower crustal pressures, while diffusion models suggest that these rims grew up to within a few months before eruption. Ascent of the primitive magma from the lower crust thus occurred over timescales much shorter than eruptive repose periods, without prolonged stalling at shallow depths. These observations are inconsistent with the view that the eruptions were entirely fed by lateral magma outflow from the shallow reservoir. They instead require some decoupling of the flow paths of the two magma types: the primitive magma either bypassed the sub-caldera reservoir laterally or ascended vertically beneath the northern vents. The two reservoirs nonetheless shared a hydraulic connection and jointly responded to rifting. Comparison of the Krafla Fires with other rifting events and eruptions highlights the complexity and diversity of magma transport during plate boundary rifting events, which is not yet captured by a generalizable model. Integration of petrologic, geochemical and geophysical data is essential to provide a holistic view of future rifting events in Iceland and at other spreading centres.<br/

    Rapid shifting of a deep magmatic source at Fagradalsfjall volcano, Iceland

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    AbstractRecent Icelandic rifting events have illuminated the roles of centralized crustal magma reservoirs and lateral magma transport1–4, important characteristics of mid-ocean ridge magmatism1,5. A consequence of such shallow crustal processing of magmas4,5 is the overprinting of signatures that trace the origin, evolution and transport of melts in the uppermost mantle and lowermost crust6,7. Here we present unique insights into processes occurring in this zone from integrated petrologic and geochemical studies of the 2021 Fagradalsfjall eruption on the Reykjanes Peninsula in Iceland. Geochemical analyses of basalts erupted during the first 50 days of the eruption, combined with associated gas emissions, reveal direct sourcing from a near-Moho magma storage zone. Geochemical proxies, which signify different mantle compositions and melting conditions, changed at a rate unparalleled for individual basaltic eruptions globally. Initially, the erupted lava was dominated by melts sourced from the shallowest mantle but over the following three weeks became increasingly dominated by magmas generated at a greater depth. This exceptionally rapid trend in erupted compositions provides an unprecedented temporal record of magma mixing that filters the mantle signal, consistent with processing in near-Moho melt lenses containing 107–108 m3 of basaltic magma. Exposing previously inaccessible parts of this key magma processing zone to near-real-time investigations provides new insights into the timescales and operational mode of basaltic magma systems.</jats:p
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