Gradual inflation of magma chambers often precedes eruptions at highly active volcanoes. During such eruptions, rapid deflation occurs as magma flows out and pressure is reduced. Less is known about the deformation style at moderately active volcanoes, such as Eyjafjallajökull, Iceland, where an explosive summit eruption of trachyandesite beginning on 14 April 2010 caused exceptional disruption to air traffic, closing airspace over much of Europe for days. This eruption was preceded by an effusive flank eruption of basalt from 20 March to 12 April 2010. The 2010 eruptions are the culmination of 18 years of intermittent volcanic unrest. Here we show that deformation associated with the eruptions was unusual because it did not relate to pressure changes within a single magma chamber. Deformation was rapid before the first eruption (>5 mm per day after 4 March), but negligible during it. Lack of distinct co-eruptive deflation indicates that the net volume of magma drained from shallow depth during this eruption was small; rather, magma flowed from considerable depth. Before the eruption, a ∼0.05 km(3) magmatic intrusion grew over a period of three months, in a temporally and spatially complex manner, as revealed by GPS (Global Positioning System) geodetic measurements and interferometric analysis of satellite radar images. The second eruption occurred within the ice-capped caldera of the volcano, with explosivity amplified by magma-ice interaction. Gradual contraction of a source, distinct from the pre-eruptive inflation sources, is evident from geodetic data. Eyjafjallajökull's behaviour can be attributed to its off-rift setting with a 'cold' subsurface structure and limited magma at shallow depth, as may be typical for moderately active volcanoes. Clear signs of volcanic unrest signals over years to weeks may indicate reawakening of such volcanoes, whereas immediate short-term eruption precursors may be subtle and difficult to detect.
We present a comprehensive set of Sr, Nd, and O isotope data and trace element concentrations from tholeiitic and alkaline lavas of the neovolcanic zones of Iceland (picrites, olivine and quartz tholeiites, transitional and alkali basalts, differentiated rocks). Variations in the oxygen isotope results allow us to distinguish two groups. The first, which comprises quartz tholeiites and more differentiated rocks usually associated with central volcanoes, has low r5180 values (+5 to + 1%o) resulting from interaction with the hydrothermally altered Icelandic crust. The second group, which contains picrites, olivine tholeiites, and alkali basalts, has normal mantle oxygen isotopic compositions (r5180 --+5 to +6%o) which are thought to represent those of the mantle source. Nd isotopic compositions vary greatly, from •43Nd/•44Nd -0.51314 in picrites to 0.51295 in alkali basalts. To produce such a variation for rocks with the chemical compositions of Icelandic volcanics (147Sm/144Nd = 0.12-0.28) requires >200 m.y., a period that greatly exceeds the maximum age of Icelandic crust. Previous models, in which the Sr isotopic variations were explained in terms of evolution of crustal reservoirs, are invalidated, and mantle reservoirs with different Nd and Sr isotopic compositions are indicated. The Iceland data define a linear array in the Sr-Nd isotope diagram which overlaps both mid-ocean ridge basalt and oceanic island basalt fields and indicates mixing between depleted and enriched end-members. Alkali basalts come preferentially from an isotopically and chemically enriched component of the Iceland plume, and picrites come from a more refractory, more depleted portion. Positive Sr, Rb, and Ba anomalies are present in picrites and other lavas with low trace element contents. These anomalies are not correlated with isotopic differences but are nevertheless believed to result from interaction between the parent magmas of these rocks and altered Icelandic crust. This indicates that even the most primitive Icelandic lavas have been contaminated with some crustal material. Pb [Hart et al., 1973; Sun and Jahn, 1975; O'Nions et al., 1977; Zindler et al., 1979]. Models proposed to explain the chemical data fall into two groups. The first requires the existence of isotopic heterogeneities in the mantle [Zindler et al., 1979]: the chemically •Now at G6osciences Marines, Ifremer-Brest, Plouzan6, France. 2Now at G6osciences, Universit6 de Rennes 1, Rennes, France. and isotopically enriched lavas come from a source within the plume; the less enriched lavas come either from another component of the plume [Elliott et al., 1991] or from the depleted source of North Atlantic MORB [Schilling, 1973; Hart et al., 1973 ; Langmuir et al., 1978]. In the second type of model a homogeneous mantle source yields magmas that interact with old, hydrothermally altered Icelandic crust during their ascent and eruption [Oskarsson et al., 1982; Steinthorsson et al., 1985; H•mond et al., 1988; Nicholson et al., 1991]. The basis of the latter type of model w...
The 1783-1784 Laki tholeiitic basalt fissure eruption in Iceland was one of the greatest atmospheric pollution events of the past 250 years, with widespread effects in the northern hemisphere. The degassing history and volatile budget of this event are determined by measurements of pre-eruption and residual contents of sulfur, chlorine, and fluorine in the products of all phases of the eruption. In fissure eruptions such as Laki, degassing occurs in two stages: by explosive activity or lava fountaining at the vents, and from the lava as it flows away from the vents. Using the measured sulfur concentrations in glass inclusions in phenocrysts and in groundmass glasses of quenched eruption products, we calculate that the total accumulative atmospheric mass loading of sulfur dioxide was 122 Mt over a period of 8 months. This volatile release is sufficient to have generated F250 Mt of H 2 SO 4 aerosols, an amount which agrees with an independent estimate of the Laki aerosol yield based on atmospheric turbidity measurements. Most of this volatile mass (F60 wt.%) was released during the first 1.5 months of activity. The measured chlorine and fluorine concentrations in the samples indicate that the atmospheric loading of hydrochloric acid and hydrofluoric acid was F7.0 and 15.0 Mt, respectively. Furthermore, F75% of the volatile mass dissolved by the Laki magma was released at the vents and carried by eruption columns to altitudes between 6 and 13 km. The high degree of degassing at the vents is attributed to development of a separated two-phase flow in the upper magma conduit, and implies that high-discharge basaltic eruptions such as Laki are able to loft huge quantities of gas to altitudes where the resulting aerosols can reside for months or even 1-2 years. The atmospheric volatile contribution due to subsequent degassing of the Laki lava flow is only 18 wt.% of the total dissolved in the magma, and these emissions were confined to the lowest regions of the troposphere and therefore important only over Iceland. This study indicates that determination of the amount of sulfur degassed from the Laki magma batch by measurements of sulfur in the volcanic products (the petrologic method) yields a result which is sufficient to account for the mass of aerosols estimated by other methods.
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