181 research outputs found
The viscosity of magmatic silicate liquids: A model for calculation
A simple model has been designed to allow reasonably accurate calculations of viscosity as a function of temperature and composition. The problem of predicting viscosities of anhydrous silicate liquids has been investigated since such viscosity numbers are applicable to many extrusive melts and to nearly dry magmatic liquids in general. The fluidizing action of water dissolved in silicate melts is well recognized and it is now possible to predict the effect of water content on viscosity in a semiquantitative way. Water was not incorporated directly into the model. Viscosities of anhydrous compositions were calculated, and, where necessary, the effect of added water and estimated. The model can be easily modified to incorporate the effect of water whenever sufficient additional data are accumulated
Lower crustal crystallization and melt evolution at mid-ocean ridges
Author Posting. © The Author(s), 2012. This is the author's version of the work. It is posted here by permission of Nature Publishing Group for personal use, not for redistribution. The definitive version was published in Nature Geoscience 5 (2012): 651–655, doi:10.1038/ngeo1552.Mid-ocean ridge magma is produced when Earth’s mantle rises beneath the ridge axis and melts as a result of the decrease in pressure. This magma subsequently undergoes cooling and crystallization to form the oceanic crust. However, there is no consensus on where within the crust or upper mantle crystallization occurs1-5. Here we provide direct geochemical evidence for the depths of crystallization beneath ridge axes of two spreading centres located in the Pacific Ocean: the fast-spreading-rate East Pacific Rise and intermediate-spreading-rate Juan de Fuca Ridge. Specifically, we measure volatile concentrations in olivine-hosted melt inclusions to derive vapour-saturation pressures and to calculate crystallisation depth. We also analyse the melt inclusions for major and trace element concentrations, allowing us to compare the distributions of crystallisation and to track the evolution of the melt during ascent through the oceanic crust. We find that most crystallisation occurs within a seismically-imaged melt lens located in the shallow crust at both ridges, but over 25% of the melt inclusions have crystallisation pressures consistent with formation in the lower oceanic crust. Furthermore, our results suggest that melts formed beneath the ridge axis can be efficiently mixed and undergo olivine crystallisation in the mantle, prior to ascent into the ocean crust.This research was supported by the National Science
Foundation (EAR-0646694) and the WHOI Deep Ocean Exploration Institute/Ocean
Ridge Initiative.2013-02-1
Explosive volcanism on the ultraslow-spreading Gakkel ridge, Arctic Ocean
Author Posting. © Nature Publishing Group, 2008. This is the author's version of the work. It is posted here by permission of Nature Publishing Group for personal use, not for redistribution. The definitive version was published in Nature 453 (2008): 1236-1238, doi:10.1038/nature07075.Roughly 60% of the Earth’s outer surface is comprised of oceanic crust formed by volcanic
processes at mid-ocean ridges (MORs). Although only a small fraction of this vast volcanic
terrain has been visually surveyed and/or sampled, the available evidence suggests that
explosive eruptions are rare on MORs, particularly at depths below the critical point for
steam (3000 m). A pyroclastic deposit has never been observed on the seafloor below 3000
m, presumably because the volatile content of mid-ocean ridge basalts is generally too low
to produce the gas fractions required to fragment a magma at such high hydrostatic
pressure. We employed new deep submergence technologies during an International Polar
Year expedition to the Gakkel Ridge in the Arctic Basin at 85°E, to acquire the first-ever
photographic images of ‘zero-age’ volcanic terrain on this remote, ice-covered MOR. Our
imagery reveals that the axial valley at 4000 m water depth is blanketed with
unconsolidated pyroclastic deposits, including bubble wall fragments (limu o Pele),
covering a large area greater than 10 km2. At least 13.5 wt% CO2 is required to fragment
magma at these depths, which is ~10x greater than the highest values measured to-date in
a MOR basalt. These observations raise important questions regarding the accumulation
and discharge of magmatic volatiles at ultra-slow spreading rates on the Gakkel Ridge (6-
14 mm yr-1, full-rate), and demonstrate that large-scale pyroclastic activity is possible
along even the deepest portions of the global MOR volcanic system.This research was
funded by the National Aeronautics and Space Administration, the National Science Foundation,
and the Woods Hole Oceanographic Institution
Fluidal pyroclasts reveal the intensity of peralkaline rhyolite pumice cone eruptions
This work is a contribution to the Natural Environment Research Council (NERC) funded RiftVolc project (NE/L013932/1, Rift volcanism: past, present and future) through which several of the authors are supported. In addition, Clarke was funded by a NERC doctoral training partnership grant (NE/L002558/1).Peralkaline rhyolites are medium to low viscosity, volatile-rich magmas typically associated with rift zones and extensional settings. The dynamics of peralkaline rhyolite eruptions remain elusive with no direct observations recorded, significantly hindering the assessment of hazard and risk. Here we describe uniquely-preserved, fluidal-shaped pyroclasts found within pumice cone deposits at Aluto, a peralkaline rhyolite caldera in the Main Ethiopian Rift. We use a combination of field-observations, geochemistry, X-ray computed microtomography (XCT) and thermal-modelling to investigate how these pyroclasts are formed. We find that they deform during flight and, depending on size, quench prior to deposition or continue to inflate then quench in-situ. These findings reveal important characteristics of the eruptions that gave rise to them: that despite the relatively low viscosity of these magmas, and similarities to basaltic scoria-cone deposits, moderate to intense, unstable, eruption columns are developed; meaning that such eruptions can generate extensive tephra-fall and pyroclastic density currents.Publisher PDFPeer reviewe
Mixing of rhyolite, trachyte and basalt magma erupted from a vertically and laterally zoned reservoir, composite flow P1, Gran Canaria
The 14.1 Ma composite welded ignimbrite P1 (45 km3 DRE) on Gran Canaria is compositionally zoned from a felsic lower part to a basaltic top. It is composed of four component magmas mixed in vertically varying proportions: (1) Na-rhyolite (10 km3) zoned from crystal-poor to highly phyric; (2) a continuously zoned, evolved trachyte to sodic trachyandesite magma group (6 km3); (3) a minor fraction of Na-poor trachyandesite (<1 km3); and (4) nearly aphyric basalt (26 km3) zoned from 4.3 to 5.2 wt% MgO. We distinguish three sites and phases of mixing: (a) Mutual mineral inclusions show that mixing between trachytic and rhyolitic magmas occurred during early stages of their intratelluric crystallization, providing evidence for long-term residence in a common reservoir prior to eruption. This first phase of mixing was retarded by increasing viscosity of the rhyolite magma upon massive anorthoclase precipitation and accumulation. (b) All component magmas probably erupted through a ring-fissure from a common upper-crustal reservoir into which the basalt intruded during eruption. The second phase of mixing occurred during simultaneous withdrawal of magmas from the chamber and ascent through the conduit. The overall withdrawal and mixing pattern evolved in response to pre-eruptive chamber zonation and density and viscosity relationships among the magmas. Minor sectorial variations around the caldera reflect both varying configurations at the conduit entrance and unsteady discharge. (c) During each eruptive pulse, fragmentation and particulate transport in the vent and as pyroclastic flows caused additional mixing by reducing the length scale of heterogeneities. Based on considerations of magma density changes during crystallization, magma temperature constraints, and the pattern of withdrawal during eruption, we propose that eruption tapped the P1 magma chamber during a transient state of concentric zonation, which had resulted from destruction of a formerly layered zonation in order to maintain gravitational equilibrium. Our model of magma chamber zonation at the time of eruption envisages a basal high-density Na-poor trachyandesite layer that was overlain by a central mass of highly phyric rhyolite magma mantled by a sheath of vertically zoned trachyte-trachyandesite magma along the chamber walls. A conventional model of vertically stacked horizontal layers cannot account for the deduced density relationships nor for the withdrawal pattern
Transfer von festen, flüssigen und gasförmigen Stoffen aus Vulkanen in die Atmosphäre
Die häufigsten vulkanischen Volatilen sind H2O, CO2, SO3 und Halogene. Zusammensetzung, Menge und Injektionsraten von vulkanischen Gasen und Partikeln in die Troposphäre und Stratosphäre hängen ab von der chemischen Zusammensetzung eines Magmas, dem plattentektonischen Milieu sowie Eruptionsmechanismen und Eruptionsraten. Über 90% der eruptierten Magmen sind basaltischer Zusammensetzung mit niedriger Viskosität, relativ geringen Volatilengehalten und meist niedrigen Eruptionsraten sowie wenig explosiven Eruptionen überwiegend entlang der mittelozeanischen Rücken in großen Wassertiefen. Magmen in Inselbögen und Subduktionszonen an Kontinenträndern sind H2O-reich, in anderen plattentektonischen Milieus überwiegt in basaltischen Magmen CO2. In mafischen Magmen ist CO2 schlecht löslich und kann daher schon mehrere Kilometer unter der Erdoberfläche als Gasphase aus einem Magma entweichen. Felsische (hochdifferenzierte) Magmen, H2O-reich und CO2-arm, eruptieren oft hochexplosiv, insbesondere an Subduktionszonen, und mit hohen Eruptionsraten, z.B. El Chichón (Mexiko, 1982) und Pinatubo (Philippinen, 1991). Ihre Eruptionssäulen (Gas-/Partikelgemische) können bis ca. 40 km Höhe erreichen und sind Hauptlieferant der in die Stratosphäre injizierten Gasmengen
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