Storage, Ascent, and Release of Silicic Magma in Caldera-forming Eruptions

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Myers, Madison Logan

The mechanisms and timescales associated with the triggering of caldera-forming eruptions remain ambiguous and poorly constrained. Do such eruptions start vigorously, then escalate, or can there be episodicity? Are they triggered through internal processes (e.g. recharge, buoyancy), or can external modulations play an important role? Key to answering these questions is the ability to reconstruct the state of the magma body immediately prior to eruption. My dissertation research seeks to answer these questions through detailed investigation of four voluminous caldera-forming eruptions: (1) 650 km3, 0.767 Ma Bishop Tuff, Long Valley, (2) 530 km3, 25.4 ka Oruanui eruption, Taupo, (3) 2,500 km3, 2.08 Ma Huckleberry Ridge Tuff, Yellowstone and (4) 250 km3, 26.91 Ma Cebolla Creek Tuff, Colorado. The main techniques I applied integrated glass geochemistry (major, trace and volatile), diffusion modeling, and detailed field sampling. In chapters two, three, and four these methods are applied to the initial fall deposits of three supereruptions (Bishop, Oruanui and Huckleberry Ridge) that preserve field-evidence for different opening behaviors. These behaviors range from continuous deposition of fall deposits and ignimbrite (Bishop), to repetitive start/stop behavior, with time breaks between eruptive episodes on the order of weeks to months (Oruanui, Huckleberry Ridge). To reconstruct the timescales of opening activity and relate this to conduit processes, I used two methods that exploit diffusion of volatiles through minerals and melt, providing estimates for the rate at which magmas ascended to the surface. This knowledge is then integrated with the pre-eruptive configuration of the magma body, based on melt inclusion chemistry, to interpret what triggered these systems into unrest. Finally, in chapter five I take a different approach by integrating geochemical data for melt inclusions and phenocryst minerals to test whether the mechanism of heat and volatile recharge

The evolution of magma during continental rifting: New constraints from the isotopic and trace element signatures of silicic magmas from Ethiopian volcanoes

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Hutchison, William; Mather, Tamsin A.; Pyle, David M.; Boyce, Adrian J.; Gleeson, Matthew L. M.; Yirgu, Gezahegn; Blundy, Jon D.; Ferguson, David J.; Vye-Brown, Charlotte; Millar, Ian L.; Sims, Kenneth W. W.; Finch, Adrian A.

2018-05-01

Magma plays a vital role in the break-up of continental lithosphere. However, significant uncertainty remains about how magma-crust interactions and melt evolution vary during the development of a rift system. Ethiopia captures the transition from continental rifting to incipient sea-floor spreading and has witnessed the eruption of large volumes of silicic volcanic rocks across the region over ∼45 Ma. The petrogenesis of these silicic rocks sheds light on the role of magmatism in rift development, by providing information on crustal interactions, melt fluxes and magmatic differentiation. We report new trace element and Sr-Nd-O isotopic data for volcanic rocks, glasses and minerals along and across active segments of the Main Ethiopian (MER) and Afar Rifts. Most δ18 O data for mineral and glass separates from these active rift zones fall within the bounds of modelled fractional crystallization trajectories from basaltic parent magmas (i.e., 5.5-6.5‰) with scant evidence for assimilation of Pan-African Precambrian crustal material (δ18 O of 7-18‰). Radiogenic isotopes (εNd = 0.92- 6.52; 87Sr/86Sr = 0.7037-0.7072) and incompatible trace element ratios (Rb/Nb productivity or where crustal structure inhibits magma ascent). This has important implications for understanding the geotectonic settings that promote extreme melt evolution and, potentially, genesis of economically-valuable mineral deposits in ancient rift-settings. The limited isotopic evidence for assimilation of Pan-African crustal material in Ethiopia suggests that the pre-rift crust beneath the magmatic segments has been substantially modified by rift-related magmatism over the past ∼45 Ma; consistent with geophysical observations. We argue that considerable volumes of crystal cumulate are stored beneath silicic volcanic systems (>100 km3), and estimate that crystal cumulates fill at least 16-30% of the volume generated by crustal extension under the axial volcanoes of the MER and Manda Hararo

Na, Rb and Cs partitioning between metal, silicate and sulfide: Implications for volatile depletion in terrestrial planets

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Boujibar, A.; Fei, Y.; Du, Z.; Righter, K.; Bullock, E. S.

2017-12-01

Inner Solar System materials are known for their depletion in volatile elements, including the moderately volatile alkalis: Na, K, Rb, and Cs. The origin of this depletion is still uncertain, as several processes could have been involved, during the nebular condensation or planetary accretion. Volatile depletion is commonly estimated through comparison of alkali concentrations relatively to those of chondrites, assuming they remain in planetary mantles during core segregation. However, experimental studies show that substantial K can partition into metals that are enriched in sulfur and oxygen. Several models have also suggested that sulfides may have played an important role during episodes of sulfide segregation from a crystallizing magma ocean (sulfide matte) or accretion of S-rich planetary embryos. For Mercury, a sulfide layer could be present between core and mantle, due to immiscibility between Si-rich and S-rich metals. Therefore, here we investigate whether alkali elements (Na, Cs and Rb) could be partly sequestered in planetary cores during their differentiation. We conducted experiments at high pressure and temperature (1 to 5 GPa and up to 1900 °C) to determine partition coefficients of Na, Rb and Cs between metal and silicate. Our results show that pressure, temperature, sulfur and oxygen in metals enhance the partitioning of Na, Rb and Cs into metals, as previously found for K. For all three investigated alkalis (Na, Rb and Cs), we found a maximum partition coefficient of 1 between sulfides containing 13 wt% O and silicate melt. Therefore, S-rich cores or sulfide layers formed due to immiscibility in Fe-S-O systems could have acted as important geochemical reservoirs for alkali elements. Using our experimental data and different assumptions on initial bulk abundances, we evaluate volatile depletion in terrestrial planets, by comparing resulting mantle alkali concentrations after core segregation, with actual concentrations in the Earth's mantle.

The influence of magma viscosity on convection within a magma chamber

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Schubert, M.; Driesner, T.; Ulmer, P.

2012-12-01

Magmatic-hydrothermal ore deposits are the most important sources of metals like Cu, Mo, W and Sn and a major resource for Au. It is well accepted that they are formed by the release of magmatic fluids from a batholith-sized magma body. Traditionally, it has been assumed that crystallization-induced volatile saturation (called "second boiling") is the main mechanism for fluid release, typically operating over thousands to tens of thousands of years (Candela, 1991). From an analysis of alteration halo geometries caused by magmatic fluids, Cathles and Shannon (2007) suggested much shorter timescales in the order of hundreds of years. Such rapid release of fluids cannot be explained by second boiling as the rate of solidification scales with the slow conduction of heat away from the system. However, rapid fluid release is possible if convection is assumed within the magma chamber. The magma would degas in the upper part of the magma chamber and volatile poor magma would sink down again. Such, the rates of degassing can be much higher than due to cooling only. We developed a convection model using Navier-Stokes equations provided by the computational fluid dynamics platform OpenFOAM that gives the possibility to use externally derived meshes with complex (natural) geometries. We implemented a temperature, pressure, composition and crystal fraction dependent viscosity (Ardia et al., 2008; Giordano et al., 2008; Moore et al., 1998) and a temperature, pressure, composition dependent density (Lange1994). We found that the new viscosity and density models strongly affect convection within the magma chamber. The dependence of viscosity on crystal fraction has a particularly strong effect as the steep viscosity increase at the critical crystal fraction leads to steep decrease of convection velocity. As the magma chamber is cooling from outside to inside a purely conductive layer is developing along the edges of the magma chamber. Convection continues in the inner part of the

Infrared Spectroscopy and Stable Isotope Geochemistry of Hydrous Silicate Glasses

Energy Technology Data Exchange (ETDEWEB)

Stolper, Edward

2007-03-05

The focus of this DOE-funded project has been the study of volatile components in magmas and the atmosphere. Over the twenty-one year period of this project, we have used experimental petrology and stable isotope geochemistry to study the behavior and properties of volatile components dissolved in silicate minerals and melts and glasses. More recently, we have also studied the concentration and isotopic composition of CO2 in the atmosphere, especially in relation to air quality issues in the Los Angeles basin.

Making mushy magma chambers in the lower continental crust: Cold storage and compositional bimodality

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Jackson, Matthew; Blundy, Jon; Sparks, Steve

2017-04-01

the local melt fraction is too low to form a mobile magma. The model results are consistent with geochemical data suggesting that lower crustal magma reservoirs supply silicic and mafic melts to arc volcanoes, but intermediate magmas are formed by mixing in shallower reservoirs. We suggest here that lower crustal magma chambers primarily form in response to changes in bulk composition caused by melt migration and chemical reaction in a mush reservoir. This process is different to the conventional and widely applied models of magma chamber formation. Similar processes are likely to operate in shallow mush reservoirs, but will likely be further complicated by the presence of volatile phases, and mixing of different melt compositions sourced from deeper mush reservoirs.

Creep of Sylramic-iBN Fiber Tows at Elevated Temperature in Air and in Silicic Acid-Saturated Steam

Science.gov (United States)

2015-06-01

CREEP OF SYLRAMIC-iBN FIBER TOWS AT ELEVATED TEMPERATURE IN AIR AND IN SILICIC ACID-SATURATED STEAM ...protection in the United States. AFIT-ENY-15-J-46 CREEP OF SYLRAMIC-iBN FIBER TOWS AT ELEVATED TEMPERATURE IN AIR AND IN SILICIC ACID-SATURATED STEAM ...DISTRIBUTION UNLIMITED. AFIT-ENY-15-J-46 CREEP OF SYLRAMIC-iBN FIBER TOWS AT ELEVATED TEMPERATURE IN AIR AND IN SILICIC ACID-SATURATED STEAM

Rapid cooling and cold storage in a silicic magma reservoir recorded in individual crystals.

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Rubin, Allison E; Cooper, Kari M; Till, Christy B; Kent, Adam J R; Costa, Fidel; Bose, Maitrayee; Gravley, Darren; Deering, Chad; Cole, Jim

2017-06-16

Silicic volcanic eruptions pose considerable hazards, yet the processes leading to these eruptions remain poorly known. A missing link is knowledge of the thermal history of magma feeding such eruptions, which largely controls crystallinity and therefore eruptability. We have determined the thermal history of individual zircon crystals from an eruption of the Taupo Volcanic Zone, New Zealand. Results show that although zircons resided in the magmatic system for 10 3 to 10 5 years, they experienced temperatures >650° to 750°C for only years to centuries. This implies near-solidus long-term crystal storage, punctuated by rapid heating and cooling. Reconciling these data with existing models of magma storage requires considering multiple small intrusions and multiple spatial scales, and our approach can help to quantify heat input to and output from magma reservoirs. Copyright © 2017, American Association for the Advancement of Science.

Storage conditions of the mafic and silicic magmas at Cotopaxi, Ecuador

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Martel, Caroline; Andújar, Joan; Mothes, Patricia; Scaillet, Bruno; Pichavant, Michel; Molina, Indira

2018-04-01

The 2015 reactivation of the Cotopaxi volcano urges us to understand the complex eruptive dynamics of Cotopaxi for better management of a potential major crisis in the near future. Cotopaxi has commonly transitioned from andesitic eruptions of strombolian style (lava flows and scoria ballistics) or nuées ardentes (pyroclastic flows and ash falls) to highly explosive rhyolitic ignimbrites (pumiceous pyroclastic flows), which entail drastically different risks. To better interpret geophysical and geochemical signals, Cotopaxi magma storage conditions were determined via existing phase-equilibrium experiments that used starting materials chemically close to the Cotopaxi andesites and rhyolites. The results suggest that Cotopaxi's most mafic andesites (last erupted products) can be stored over a large range of depth from 7 km to ≥16 km below the summit (pressure from 200 to ≥400 MPa), 1000 °C, NNO +2, and contain 4.5-6.0±0.7 wt% H2O dissolved in the melt in equilibrium with 30-40% phenocrysts of plagioclase, two pyroxenes, and Fe-Ti oxides. These mafic andesites sometimes evolve towards more silicic andesites by cooling to 950 °C. Rhyolitic magmas are stored at 200-300 MPa (i.e. 7-11 km below the summit), 750 °C, NNO +2, and contain 6-8 wt% H2O dissolved in a nearly aphyric melt (<5% phenocrysts of plagioclase, biotite, and Fe-Ti oxides). Although the andesites produce the rhyolitic magmas by fractional crystallization, the Cotopaxi eruptive history suggests reactivation of either reservoirs at distinct times, likely reflecting flux or time fluctuations during deep magma recharge.

Magma buoyancy and volatile ascent driving autocyclic eruptivity at Hekla Volcano (Iceland)

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Hautmann, Stefanie; Sacks, I. Selwyn; Linde, Alan T.; Roberts, Matthew J.

2017-09-01

Volcanic eruptions are typically accompanied by ground deflation due to the withdrawal of magma from depth and its effusion at the surface. Here, based on continuous high-resolution borehole strain data, we show that ground deformation was absent during the major effusion phases of the 1991 and 2000 eruptions of Hekla Volcano, Iceland. This lack of surface deformation challenges the classic model of magma intrusion/withdrawal as source for volcanic ground uplift/subsidence. We incorporate geodetic and geochemical observables into theoretical models of magma chamber dynamics in order to constrain quantitatively alternative co- and intereruptive physical mechanisms that govern magma propagation and system pressurization. We find the lack of surface deformation during lava effusion to be linked to chamber replenishment from below whilst magma migrates as a buoyancy-driven flow from the magma chamber towards the surface. We further demonstrate that intereruptive pressure build-up is likely to be generated by volatile ascent within the chamber rather than magma injection. Our model explains the persistent periodic eruptivity at Hekla throughout historic times with self-initiating cycles and is conceptually relevant to other volcanic systems.

A volatile topic: Parsing out the details of Earth's formation through experimental metal-silicate partitioning of volatile and moderately volatile elements

Science.gov (United States)

Mahan, B. M.; Siebert, J.; Blanchard, I.; Badro, J.; Sossi, P.; Moynier, F.

2017-12-01

Volatile and moderately volatile elements display different volatilities and siderophilities, as well as varying sensitivity to thermodynamic controls (X, P, T, fO2) during metal-silicate differentiation. The experimental determination of the metal-silicate partitioning of these elements permits us to evaluate processes controlling the distribution of these elements in Earth. In this work, we have combined metal-silicate partitioning data and results for S, Sn, Zn and Cu, and input these characterizations into Earth formation models. Model parameters such as source material, timing of volatile delivery, fO2 path, and degree of impactor equilibration were varied to encompass an array of possible formation scenarios. These models were then assessed to discern plausible sets of conditions that can produce current observed element-to-element ratios (e.g. S/Zn) in the Earth's present-day mantle, while also satisfying current estimates on the S content of the core, at no more than 2 wt%. The results of our models indicate two modes of accretion that can maintain chondritic element-to-element ratios for the bulk Earth and can arrive at present-day mantle abundances of these elements. The first mode requires the late addition of Earth's entire inventory of these elements (assuming a CI-chondritic composition) and late-stage accretion that is marked by partial equilibration of large impactors. The second, possibly more intuitive mode, requires that Earth accreted - at least initially - from volatile poor material preferentially depleted in S relative to Sn, Zn, and Cu. From a chemical standpoint, this source material is most similar to type I chondrule rich (and S poor) materials (Hewins and Herzberg, 1996; Mahan et al., 2017; Amsellem et al., 2017), such as the metal-bearing carbonaceous chondrites.

Chemistry of the subalkalic silicic obsidians

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MacDonald, Ray; Smith, Robert L.; Thomas, John E.

1992-01-01

Nonhydrated obsidians are quenched magmatic liquids that record in their chemical compositions details of the tectonic environment of formation and of the differentiation mechanisms that affected their subsequent evolution. This study attempts to analyze, in terms of geologic processes, the compositional variations in the subalkalic silicic obsidians (Si02≥70 percent by weight, molecular (Na2O+K20)>Al2O3). New major- and trace-element determinations of 241 samples and a compilation of 130 published major-element analyses are reported and interpreted. Obsidians from five different tectonic settings are recognized: (1) primitive island arcs, (2) mature island arcs, (3) continental margins, (4) continental interiors, and (5) oceanic extensional zones. Tectonomagmatic discrimination between these groups is successfully made on Nb-Ta, Nb-FeOt and Th-Hf-Ta plots, and compositional ranges and averages for each group are presented. The chemical differences between groups are related to the type of crust in which magmas were generated. With increasingly sialic (continental type) crust, the obsidians show overall enrichment in F, Be, Li, Mo, Nb, Rb, Sn, Ta, U, W, Zn, and the rare-earth elements, and depletion in Mg, Ca, Ba, Co, Sc, Sr, and Zr. They become more potassic, have higher Fe/Mg and F/Cl ratios, and lower Zr/Hf, Nb/Ta, and Th/U ratios. Higher values of total rare-earth elements are accompanied by light rare-earth-element enrichment and pronounced negative Eu anomalies. An attempt is made to link obsidian chemistry to genetic mechanlism. Two broad groups of rocks are distinguished: one generated where crystal-liquid processes dominated (CLPD types), which are the products of crustal anatexis, possibly under conditions of low halogen fugacity, ± crystal fractionation ± magma mixing; and a second group represented by rocks formed in the upper parts of large magma chambers by interplays of crystal fractionation, volatile transfer, magma mixing, and possibly various

Degassing during magma ascent in the Mule Creek vent (USA)

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Stasiuk, M.V.; Barclay, J.; Carroll, M.R.; Jaupart, Claude; Ratte, J.C.; Sparks, R.S.J.; Tait, S.R.

1996-01-01

The structures and textures of the rhyolite in the Mule Creek vent (New Mexico, USA) indicate mechanisms by which volatiles escape from silicic magma during eruption. The vent outcrop is a 300-m-high canyon wall comprising a section through the top of a feeder conduit, vent and the base of an extrusive lava dome. Field relations show that eruption began with an explosive phase and ended with lava extrusion. Analyses of glass inclusions in quartz phenocrysts from the lava indicate that the magma had a pre-eruptive dissolved water content of 2.5-3.0 wt% and, during eruption, the magma would have been water-saturated over the vertical extent of the present outcrop. However, the vesicularity of the rhyolite is substantially lower than that predicted from closed-system models of vesiculation under equilibrium conditions. At a given elevation in the vent, the volume fraction of primary vesicles in the rhyolite increases from zero close to the vent margin to values of 20-40 vol.% in the central part. In the centre the vesicularity increases upward from approximately 20 vol.% at 300 m below the canyon rim to approximately 40 vol.% at 200 m, above which it shows little increase. To account for the discrepancy between observed vesicularity and measured water content, we conclude that gas escaped during ascent, probably beginning at depths greater than exposed, by flow through the vesicular magma. Gas escape was most efficient near the vent margin, and we postulate that this is due both to the slow ascent of magma there, giving the most time for gas to escape, and to shear, favouring bubble coalescence. Such shear-related permeability in erupting magma is supported by the preserved distribution of textures and vesicularity in the rhyolite: Vesicles are flattened and overlapping near the dense margins and become progressively more isolated and less deformed toward the porous centre. Local zones have textures which suggest the coalescence of bubbles to form permeable

Diffusive exchange of trace elements between basaltic-andesite and dacitic melt: Insights into potential metal fractionation during magma mixing

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Fiege, A.; Ruprecht, P.; Simon, A. C.; Holtz, F.

2017-12-01

Mafic magma recharge is a common process that triggers physical and chemical mixing in magmatic systems and drives their evolution, resulting in, e.g., hybridization and volcanic eruptions. Once magma-magma contact is initiated, rapid heat-flux commonly leads to the formation of a cooling-induced crystal mush on the mafic side of the interface. Here, on a local scale (µm to cm), at the magma-magma interface, melt-melt diffusive exchange is required to approach equilibrium. Significant chemical potential gradients drive a complex, multi-element mass flux between the two systems (Liang, 2010). This diffusive-equilibration often controls crystal dissolution rates within the boundary layers and, thus, the formation of interconnected melt or fluid networks. Such networks provide important pathways for the transport of volatiles and trace metals from the mafic recharge magma to the felsic host magma, where the latter may feed volcanic activities and ore deposits. While major element diffusion in silicate melts is mostly well understood, even in complex systems, the available data for many trace element metals are limited (Liang, 2010; Zhang et al., 2010). Differences in diffusivity in a dynamic, mixing environment can cause trace element fractionation, in particular during crystallization and volatile exsolution and separation. This may affect trace element signatures in phenocrysts and magmatic volatile phases that can form near a magma-magma boundary. As a result, the chemistry of volcanic gases and magmatic-hydrothermal ore deposits may be partially controlled by such mixing phenomena. We performed melt-melt diffusion-couple experiments at 150 MPa, 1100°C, FMQ, FMQ+1 and FMQ+3 (FMQ: fayalite-magnetite-quartz oxygen fugacity buffer). Hydrated, sulfur-bearing cylinders of dacite and basaltic andesite were equilibrated for up to 20 h. Major and trace element gradients were measured by using laser-ablation ICP-MS and electron microprobe analyses. The results we will

Using experimental petrology to constrain genesis of wet, silicic magmas in the Tonga-Kermadec island arc

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Brens, R.; Rushmer, T. A.; Turner, S.; Adam, J.

2012-12-01

The Tongan arc system is comprised of a pair of island chains, where the western chain is the active volcanic arc. A range of rock suites, from basaltic andesites (53-56% SiO2) to dacites (64-66% SiO2), has been recovered from Late, Tofua and Fonualei in the Tonga-Kermadec primitive island arc system. For which the question arises: What is the mechanism that allows for silicic magmas to develop in a primitive island arc system? Caufield et al. (2012) suggest that fractional crystallization of a multi magma chamber process, with varying depth, is responsible for the silicic magma generation in this arc. Models such as this one have been proposed and experimentally tested in other systems (Novarupta, Alaska) to explain the origin of these silicic rocks. Our Tongan suite of rocks has had a full geochemical analysis for majors, traces and isotopes. The lavas from Tofua and Late are Fe-rich and have low concentrations of K, Rb, Ba, Zr, REE, Pb and U. However, experimental studies are needed to complement the extensive geochemical analysis done on the Tongan arc. Former geochemical work done on the igneous rocks from both of these volcanic suites from this arc suggests that the source of these rocks extend from 1.5-5.5 km in depth (Caulfield et al., 2012). Here, we present an experimental study of the phase equilibria on a natural andesitic sample (Late 1, from Ewart et al., 1975) from the island of Late. Experiments were run using the temperature constraints between 900 to 1220oC, pressure from 5 to 25 kbars and H2O addition of mostly 5wt% (but some results were obtained at 2wt% in the rocks). In the presence of 5 wt% water, phase equilibria of these experiments show the garnet stability field at >10 kb for 900 oC and increases with increasing temperature, while plagioclase enters at lower pressures when garnet exits. Experimental results currently suggests, at lower temperatures (900-950oC), a fractional crystallization relationship due to shallow level pressures of

Differentiation of Asteroid 4 Vesta: Core Formation by Iron Rain in a Silicate Magma Ocean

Science.gov (United States)

Kiefer, Walter S.; Mittlefehldt, David W.

2017-01-01

Geochemical observations of the eucrite and diogenite meteorites, together with observations made by NASA's Dawn spacecraft while orbiting asteroid 4 Vesta, suggest that Vesta resembles H chondrites in bulk chemical composition, possible with about 25 percent of a CM-chondrite like composition added in. For this model, the core is 15 percent by mass (or 8 percent by volume) of the asteroid, with a composition of 73.7 percent by weight Fe, 16.0 percent by weight S, and 10.3 percent by weight Ni. The abundances of moderately siderophile elements (Ni, Co, Mo, W, and P) in eucrites require that essentially all of the metallic phase in Vesta segregated to form a core prior to eucrite solidification. The combination of the melting phase relationships for the silicate and metal phases, together with the moderately siderophile element concentrations together require that complete melting of the metal phase occurred (temperature is greater than1350 degrees Centigrade), along with substantial (greater than 40 percent) melting of the silicate material. Thus, core formation on Vesta occurs as iron rain sinking through a silicate magma ocean.

Chemical Zoning of Feldspars in Lunar Granitoids: Implications for the Origins of Lunar Silicic Magmas

Science.gov (United States)

Mills, R. D; Simon, J. I.; Alexander, C.M. O'D.; Wang, J.; Christoffersen, R.; Rahman, Z..

2014-01-01

Fine-scale chemical and textural measurements of alkali and plagioclase feldspars in the Apollo granitoids (ex. Fig. 1) can be used to address their petrologic origin(s). Recent findings suggest that these granitoids may hold clues of global importance, rather than of only local significance for small-scale fractionation. Observations of morphological features that resemble silicic domes on the unsampled portion of the Moon suggest that local, sizable net-works of high-silica melt (>65 wt % SiO2) were present during crust-formation. Remote sensing data from these regions suggest high concentrations of Si and heat-producing elements (K, U, and Th). To help under-stand the role of high-silica melts in the chemical differentiation of the Moon, three questions must be answered: (1) when were these magmas generated?, (2) what was the source material?, and (3) were these magmas produced from internal differentiation. or impact melting and crystallization? Here we focus on #3. It is difficult to produce high-silica melts solely by fractional crystallization. Partial melting of preexisting crust may therefore also have been important and pos-sibly the primary mechanism that produced the silicic magmas on the Moon. Experimental studies demonstrate that partial melting of gabbroic rock under mildly hydrated conditions can produce high-silica compositions and it has been suggested by that partial melting by basaltic underplating is the mechanism by which high-silica melts were produced on the Moon. TEM and SIMS analyses, coordinated with isotopic dating and tracer studies, can help test whether the minerals in the Apollo granitoids formed in a plutonic setting or were the result of impact-induced partial melting. We analyzed granitoid clasts from 3 Apollo samples: polymict breccia 12013,141, crystalline-matrix breccia 14303,353, and breccia 15405,78

Sulfur concentration at sulfide saturation (SCSS) in magmatic silicate melts

Science.gov (United States)

Liu, Yanan; Samaha, Naji-Tom; Baker, Don R.

2007-04-01

The sulfur concentration in silicate melts at sulfide saturation (SCSS) was experimentally investigated in a temperature range from 1150 to 1450 °C and a pressure range from 500 MPa to 1 GPa in a piston-cylinder apparatus. The investigated melt compositions varied from rhyolitic to basaltic and water concentrations varied from 0 to ˜9 wt%. All experiments were saturated with FeS melt or pyrrhotite crystals. Temperature was confirmed to have a positive effect on the SCSS. Experimental oxygen fugacities were either near the carbon-carbon monoxide buffer or one log unit above the nickel-nickel oxide buffer, and found to positively affect the SCSS. Combining our results with data from the literature we constructed a model to predict the SCSS in melts ranging in composition from komatiitic to rhyolitic, with water concentrations from 0 to 9 wt%, at pressures from 1 bar to 9 GPa and oxygen fugacities between ˜2 log units below the fayalite-magnetite-quartz buffer to ˜2 log units above it. The coefficients were obtained by multiple linear regression of experimental data and the best model found for the prediction of the SCSS is: ln(Sinppm)=11.35251-{4454.6}/{T}-0.03190{P}/{T}+0.71006ln(MFM)-1.98063[(MFM)(XO)]+0.21867ln(XO)+0.36192lnX where P is in bar, T is in K, MFM is a compositional parameter describing the melt based upon cation mole fractions: MFM={Na+K+2(Ca+Mg+Fe)}/{Si×(Al+Fe)}, XO is the mole fraction of water in the melt, and X is the mole fraction of FeO in the melt. This model was independently tested against experiments performed on anhydrous and hydrous melts in the temperature range from 800 to 1800 °C and 1-9 GPa. The model typically predicts the measured values of the natural log of the SCSS (in ppm) for komatiitic to rhyolitic (˜42 to ˜74 wt% SiO 2) melts to within 5% relative, but is less accurate for high-silica (>76 wt% SiO 2) rhyolites, especially those with molar ratios of iron to sulfur below 2. We demonstrate how this model can be used with

Silicate melts density, buoyancy relations and the dynamics of magmatic processes in the upper mantle

Science.gov (United States)

Sanchez-Valle, Carmen; Malfait, Wim J.

2016-04-01

Although silicate melts comprise only a minor volume fraction of the present day Earth, they play a critical role on the Earth's geochemical and geodynamical evolution. Their physical properties, namely the density, are a key control on many magmatic processes, including magma chamber dynamics and volcanic eruptions, melt extraction from residual rocks during partial melting, as well as crystal settling and melt migration. However, the quantitative modeling of these processes has been long limited by the scarcity of data on the density and compressibility of volatile-bearing silicate melts at relevant pressure and temperature conditions. In the last decade, new experimental designs namely combining large volume presses and synchrotron-based techniques have opened the possibility for determining in situ the density of a wide range of dry and volatile-bearing (H2O and CO2) silicate melt compositions at high pressure-high temperature conditions. In this contribution we will illustrate some of these progresses with focus on recent results on the density of dry and hydrous felsic and intermediate melt compositions (rhyolite, phonolite and andesite melts) at crustal and upper mantle conditions (up to 4 GPa and 2000 K). The new data on felsic-intermediate melts has been combined with in situ data on (ultra)mafic systems and ambient pressure dilatometry and sound velocity data to calibrate a continuous, predictive density model for hydrous and CO2-bearing silicate melts with applications to magmatic processes down to the conditions of the mantle transition zone (up to 2773 K and 22 GPa). The calibration dataset consist of more than 370 density measurements on high-pressure and/or water-and CO2-bearing melts and it is formulated in terms of the partial molar properties of the oxide components. The model predicts the density of volatile-bearing liquids to within 42 kg/m3 in the calibration interval and the model extrapolations up to 3000 K and 100 GPa are in good agreement

Mafic-silicic magma interaction in the layered 1.87 Ga Soukkio Complex in Mäntsälä, southern Finland

Directory of Open Access Journals (Sweden)

Toni T. Eerola

2002-01-01

Full Text Available The Svecofennian layered Soukkio Complex (1.87 Ga in Mäntsälä, southern Finland, consists of layered tholeiitic gabbro and porphyritic calc-alkaline monzonite, quartz monzonite and granite, mingled together. The gabbro belongs to a group of ten mafic-ultramafic intrusions of Mäntsälä, part of the 150 km long and 20 km wide, linear, E-W trending Hyvinkää–Mäntsälä Gabbroic Belt(HMGB, representing syn-collisional magmatism. Structures and textures related to magma mingling and mixing occur in a 1–2 km wide zone around Lake Kilpijärvi, located at the center of the Soukkio Complex. The complex is compositionally stratified and consists of four zones:its base, found at the Western Zone, is a dynamically layered gabbro. The followingtonalite is probably a result of magma mixing. Felsic amoeboid layers and pipes, alternating with or cutting the fine-grained gabbro in the Central-Western Zone, resemble those of mafic-silicic layered intrusions in general. Mafic magmatic enclaves (MMEs and pillows form the South-Central Zone and disrupted synplutonic mafic dykes or sheets intruded the granite in the Eastern Zone. The MMEs and disrupted synplutonic mafic dykes or sheets show cuspate and chilled margins against the felsic host, quartz ocelli, corroded K-feldspar xenocrysts with or without plagioclase mantles, and acicular apatite, all typical features of magma mingling and mixing. Mixing is suggested by intermediate composition of MMEs between granitoid and gabbro, as well as by their partly linear trends in some Harker diagrams. REE composition of the MMEs is similar to that of the Soukkio Gabbro, as expected for granite hosted MMEs. The model proposed for evolution of the Soukkio Complex involves intrusion of mafic magma into the crust, causing its partial melting. This generated granitic magma above the mafic chamber. Injections of mafic magma invaded the felsic chamber and those magmas interacted mainly by intermingling. Mingling and

The crustal magma storage system of Volcán Quizapu, Chile, and the effects of magma mixing on magma diversity

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Bergantz, George W.; Cooper, Kari M.; Hildreth, Edward; Ruprecht, Phillipp

2012-01-01

Crystal zoning as well as temperature and pressure estimates from phenocryst phase equilibria are used to constrain the architecture of the intermediate-sized magmatic system (some tens of km3) of Volcán Quizapu, Chile, and to document the textural and compositional effects of magma mixing. In contrast to most arc magma systems, where multiple episodes of open-system behavior obscure the evidence of major magma chamber events (e.g. melt extraction, magma mixing), the Quizapu magma system shows limited petrographic complexity in two large historical eruptions (1846–1847 and 1932) that have contrasting eruptive styles. Quizapu magmas and peripheral mafic magmas exhibit a simple binary mixing relationship. At the mafic end, basaltic andesite to andesite recharge magmas complement the record from peripheral cones and show the same limited range of compositions. The silicic end-member composition is almost identical in both eruptions of Quizapu. The effusive 1846–1847 eruption records significant mixing between the mafic and silicic end-members, resulting in hybridized andesites and mingled dacites. These two compositionally simple eruptions at Volcán Quizapu present a rare opportunity to isolate particular aspects of magma evolution—formation of homogeneous dacite magma and late-stage magma mixing—from other magma chamber processes. Crystal zoning, trace element compositions, and crystal-size distributions provide evidence for spatial separation of the mafic and silicic magmas. Dacite-derived plagioclase phenocrysts (i.e. An25–40) show a narrow range in composition and limited zonation, suggesting growth from a compositionally restricted melt. Dacite-derived amphibole phenocrysts show similar restricted compositions and furthermore constrain, together with more mafic amphibole phenocrysts, the architecture of the magmatic system at Volcán Quizapu to be compositionally and thermally zoned, in which an andesitic mush is overlain by a homogeneous dacitic

Direct evidence for the origin of low-18O silicic magmas: Quenched samples of a magma chamber's partially-fused granitoid walls, Crater Lake, Oregon

International Nuclear Information System (INIS)

Bacon, C.R.; Adami, L.H.; Lanphere, M.A.

1989-01-01

Partially fused granitoid blocks were ejected in the climactic eruption of Mount Mazama, which was accompanied by collapse of Crater Lake caldera. Quartz, plagioclase, and glass in the granitoids have much lower δ 18 O values (-3.4 to +4.9per mille) than any fresh lavas of Mount Mazama and the surrounding region (+5.8 to +7.0per mille). Oxygen isotope fractionation between phases in granitoids is consistent with equilibrium at T≥900deg C following subsolidus exchange with hydrothermal fluids of meteoric origin. Assimilation of ≅ 10-20% of material similar to these granitoids can account for the O and Sr isotopic compositions of lavas and juvenile pyroclasts derived from the climactic magma chamber, many of which have δ 18 O values ≅ 0.5per mille or more lower than comparable lavas of Mount Mazama. The O isotope data provide the only clear evidence for such assimilation because the mineralogy and chemical and radiogenic isotopic compositions of the granitoids (dominantly granodiorite) are similar to those of erupted juvenile magmas. The granitoid blocks from Crater Lake serve as direct evidence for the origin of 18 O depletion in large, shallow silicic magma bodies. (orig.)

Volatile-induced magma differentiation in the plumbing system of Mt. Etna volcano (Italy): evidence from glass in tephra of the 2001 eruption

Science.gov (United States)

Ferlito, Carmelo; Viccaro, Marco; Cristofolini, Renato

2008-02-01

Mount Etna volcano was shaken during the summer 2001 by one of the most singular eruptive episodes of the last centuries. For about 3 weeks, several eruptive fractures developed, emitting lava flows and tephra that significantly modified the landscape of the southern flank of the volcano. This event stimulated the attention of the scientific community especially for the simultaneous emission of petrologically distinct magmas, recognized as coming from different segments of the plumbing system. A stratigraphically controlled sampling of tephra layers was performed at the most active vents of the eruption, in particular at the 2,100 m (CAL) and at the 2,550 m (LAG) scoria cones. Detailed scanning electron microscope and energy dispersive x-ray spectrometer (SEM-EDS) analyses performed on glasses found in tephra and comparison with lava whole rock compositions indicate an anomalous increase in Ti, Fe, P, and particularly of K and Cl in the upper layers of the LAG sequence. Mass balance and thermodynamic calculations have shown that this enrichment cannot be accounted for by “classical” differentiation processes, such as crystal fractionation and magma mixing. The analysis of petrological features of the magmas involved in the event, integrated with the volcanological evolution, has evidenced the role played by volatiles in controlling the magmatic evolution within the crustal portion of the plumbing system. Volatiles, constituted of H2O, CO2, and Cl-complexes, originated from a deeply seated magma body (DBM). Their upward migration occurred through a fracture network possibly developed by the seismic swarms during the period preceding the event. In the upper portion of the plumbing system, a shallower residing magma body (ABT) had chemical and physical conditions to receive migrating volatiles, which hence dissolved the mobilized elements producing the observed selective enrichment. This volatile-induced differentiation involved exclusively the lowest erupted

Volatile diffusion in silicate melts and its effects on melt inclusions

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P. Scarlato

2005-06-01

Full Text Available A compendium of diffusion measurements and their Arrhenius equations for water, carbon dioxide, sulfur, fluorine, and chlorine in silicate melts similar in composition to natural igneous rocks is presented. Water diffusion in silicic melts is well studied and understood, however little data exists for melts of intermediate to basic compositions. The data demonstrate that both the water concentration and the anhydrous melt composition affect the diffusion coefficient of water. Carbon dioxide diffusion appears only weakly dependent, at most, on the volatilefree melt composition and no effect of carbon dioxide concentration has been observed, although few experiments have been performed. Based upon one study, the addition of water to rhyolitic melts increases carbon dioxide diffusion by orders of magnitude to values similar to that of 6 wt% water. Sulfur diffusion in intermediate to silicic melts depends upon the anhydrous melt composition and the water concentration. In water-bearing silicic melts sulfur diffuses 2 to 3 orders of magnitude slower than water. Chlorine diffusion is affected by both water concentration and anhydrous melt composition; its values are typically between those of water and sulfur. Information on fluorine diffusion is rare, but the volatile-free melt composition exerts a strong control on its diffusion. At the present time the diffusion of water, carbon dioxide, sulfur and chlorine can be estimated in silicic melts at magmatic temperatures. The diffusion of water and carbon dioxide in basic to intermediate melts is only known at a limited set of temperatures and compositions. The diffusion data for rhyolitic melts at 800°C together with a standard model for the enrichment of incompatible elements in front of growing crystals demonstrate that rapid crystal growth, greater than 10-10 ms-1, can significantly increase the volatile concentrations at the crystal-melt interface and that any of that melt trapped

Crustal thermal state and origin of silicic magma in Iceland: the case of Torfajökull, Ljósufjöll and Snæfellsjökull volcanoes

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Martin, E.; Sigmarsson, O.

2007-05-01

Pleistocene and Holocene peralkaline rhyolites from Torfajökull (South Iceland Volcanic Zone) and Ljósufjöll central volcanoes and trachytes from Snæfellsjökull (Snæfellsnes Volcanic Zone) allow the assessment of the mechanism for silicic magma genesis as a function of geographical location and crustal geothermal gradient. The low δ18O (2.4‰) and low Sr concentration (12.2 ppm) measured in Torfajökull rhyolites are best explained by partial melting of hydrated metabasaltic crust followed by major fractionation of feldspar. In contrast, very high 87Sr/86Sr (0.70473) and low Ba (8.7 ppm) and Sr (1.2 ppm) concentrations measured in Ljósufjöll silicic lavas are best explained by fractional crystallisation and subsequent 87Rb decay. Snæfellsjökull trachytes are also generated by fractional crystallisation, with less than 10% crustal assimilation, as inferred from their δ18O. The fact that silicic magmas within, or close to, the rift zone are principally generated by crustal melting whereas those from off-rift zones are better explained by fractional crystallisation clearly illustrates the controlling influence of the thermal state of the crust on silicic magma genesis in Iceland.

Magma mixing and the generation of isotopically juvenile silicic magma at Yellowstone caldera inferred from coupling 238U–230Th ages with trace elements and Hf and O isotopes in zircon and Pb isotopes in sanidine

Science.gov (United States)

Stelten, Mark E.; Cooper, Kari M.; Vazquez, Jorge A.; Reid, Mary R.; Barfod, Gry H.; Wimpenny, Josh; Yin, Qing-Zhu

2013-01-01

The nature of compositional heterogeneity within large silicic magma bodies has important implications for how silicic reservoirs are assembled and evolve through time. We examine compositional heterogeneity in the youngest (~170 to 70 ka) post-caldera volcanism at Yellowstone caldera, the Central Plateau Member (CPM) rhyolites, as a case study. We compare 238U–230Th age, trace-element, and Hf isotopic data from zircons, and major-element, Ba, and Pb isotopic data from sanidines hosted in two CPM rhyolites (Hayden Valley and Solfatara Plateau flows) and one extracaldera rhyolite (Gibbon River flow), all of which erupted near the caldera margin ca. 100 ka. The Hayden Valley flow hosts two zircon populations and one sanidine population that are consistent with residence in the CPM reservoir. The Gibbon River flow hosts one zircon population that is compositionally distinct from Hayden Valley flow zircons. The Solfatara Plateau flow contains multiple sanidine populations and all three zircon populations found in the Hayden Valley and Gibbon River flows, demonstrating that the Solfatara Plateau flow formed by mixing extracaldera magma with the margin of the CPM reservoir. This process highlights the dynamic nature of magmatic interactions at the margins of large silicic reservoirs. More generally, Hf isotopic data from the CPM zircons provide the first direct evidence for isotopically juvenile magmas contributing mass to the youngest post-caldera magmatic system and demonstrate that the sources contributing magma to the CPM reservoir were heterogeneous in 176Hf/177Hf at ca. 100 ka. Thus, the limited compositional variability of CPM glasses reflects homogenization occurring within the CPM reservoir, not a homogeneous source.

Solubility of C-O-H volatiles in graphite-saturated martian basalts and application to martian atmospheric evolution

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Stanley, B. D.; Hirschmann, M. M.; Withers, A. C.

2012-12-01

The modern martian atmosphere is thin, leading to surface conditions too cold to support liquid water. Yet, there is evidence of liquid surface water early in martian history that is commonly thought to require a thick CO2 atmosphere. Our previous work follows the analysis developed by Holloway and co-workers (Holloway et al. 1992; Holloway 1998), which predicts a linear relationship between CO2 and oxygen fugacity (fO2) in graphite-saturated silicate melts. At low oxygen fugacity, the solubility of CO2 in silicate melts is therefore very low. Such low calculated solubilities under reducing conditions lead to small fluxes of CO2 associated with martian magmatism, and therefore production of a thick volcanogenic CO2 atmosphere could require a prohibitively large volume of mantle-derived magma. The key assumption in these previous calculations is that the carbonate ion is the chief soluble C-O-H species. The results of the calculations would not be affected appreciably if molecular CO2, rather than carbonate ion, were an important species, but could be entirely different if there were other appreciable C-species such as CO, carbonyl (C=O) complexes, carbide (Si-C), or CH4. Clearly, graphite-saturated experiments are required to explore how much volcanogenic C may be degassed by reduced martian lavas. A series of piston-cylinder experiments were performed on synthetic martian starting materials over a range of oxygen fugacities (IW+2.3 to IW-0.9), and at pressures of 1-3 GPa and temperatures of 1340-1600 °C in Pt-graphite double capsules. CO2 contents in experimental glasses were determined using Fourier transform infrared spectroscopy (FTIR) and range from 0.0026-0.50 wt%. CO2 solubilities change by one order of magnitude with an order of magnitude change in oxygen fugacity, as predicted by previous work. Secondary ion mass spectrometry (SIMS) determinations of C contents in glasses range from 0.0131-0.2626 wt%. C contents determined by SIMS are consistently higher

Location of silicic caldera formation in arc settings

Energy Technology Data Exchange (ETDEWEB)

Hughes, Gwyneth R; Mahood, Gail A [Department of Geological and Environmental Sciences, Stanford University, 450 Serra, Mall, Building 320, Stanford, CA 94305-2115 (United States)

2008-10-01

Silicic calderas are the surface expressions of silicic magma chambers, and thus their study may yield information about what tectonic and crustal features favor the generation of evolved magma. The goal of this study is to determine whether silicic calderas in arc settings are preferentially located behind the volcanic front. After a global analysis of young, arc-related calderas, we find that silicic calderas at continental margins do form over a wide area behind the front, as compared to other types of arc volcanoes.

Magmas near the critical degassing pressure drive volcanic unrest towards a critical state

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Chiodini, Giovanni; Paonita, Antonio; Aiuppa, Alessandro; Costa, Antonio; Caliro, Stefano; De Martino, Prospero; Acocella, Valerio; Vandemeulebrouck, Jean

2016-01-01

During the reawaking of a volcano, magmas migrating through the shallow crust have to pass through hydrothermal fluids and rocks. The resulting magma–hydrothermal interactions are still poorly understood, which impairs the ability to interpret volcano monitoring signals and perform hazard assessments. Here we use the results of physical and volatile saturation models to demonstrate that magmatic volatiles released by decompressing magmas at a critical degassing pressure (CDP) can drive volcanic unrest towards a critical state. We show that, at the CDP, the abrupt and voluminous release of H2O-rich magmatic gases can heat hydrothermal fluids and rocks, triggering an accelerating deformation that can ultimately culminate in rock failure and eruption. We propose that magma could be approaching the CDP at Campi Flegrei, a volcano in the metropolitan area of Naples, one of the most densely inhabited areas in the world, and where accelerating deformation and heating are currently being observed. PMID:27996976

Geochemistry and volatile content of magmas feeding explosive eruptions at Telica volcano (Nicaragua)

Science.gov (United States)

Robidoux, P.; Rotolo, S. G.; Aiuppa, A.; Lanzo, G.; Hauri, E. H.

2017-07-01

Telica volcano, in north-west Nicaragua, is a young stratovolcano of intermediate magma composition producing frequent Vulcanian to phreatic explosive eruptions. The Telica stratigraphic record also includes examples of (pre)historic sub-Plinian activity. To refine our knowledge of this very active volcano, we analyzed major element composition and volatile content of melt inclusions from some stratigraphically significant Telica tephra deposits. These include: (1) the Scoria Telica Superior (STS) deposit (2000 to 200 years Before Present; Volcanic Explosive Index, VEI, of 2-3) and (2) pyroclasts from the post-1970s eruptive cycle (1982; 2011). Based on measurements with nanoscale secondary ion mass spectrometry, olivine-hosted (forsterite [Fo] > 80) glass inclusions fall into 2 distinct clusters: a group of H2O-rich (1.8-5.2 wt%) inclusions, similar to those of nearby Cerro Negro volcano, and a second group of CO2-rich (360-1700 μg/g CO2) inclusions (Nejapa, Granada). Model calculations show that CO2 dominates the equilibrium magmatic vapor phase in the majority of the primitive inclusions (XCO2 > 0.62-0.95). CO2, sulfur (generally 400 MPa) and early crystallization of magmas. Chlorine exhibits a wide concentration range (400-2300 μg/g) in primitive olivine-entrapped melts (likely suggesting variable source heterogeneity) and is typically enriched in the most differentiated melts (1000-3000 μg/g). Primitive, volatile-rich olivine-hosted melt inclusions (entrapment pressures, 5-15 km depth) are exclusively found in the largest-scale Telica eruptions (exemplified by STS in our study). These eruptions are thus tentatively explained as due to injection of deep CO2-rich mafic magma into the shallow crustal plumbing system. More recent (post-1970), milder (VEI 1-2) eruptions, instead, do only exhibit evidence for low-pressure (P viscosity of resident magma in shallow plumbing system (< 2.4 km), due to crystallization and degassing.

Derivation of intermediate to silicic magma from the basalt analyzed at the Vega 2 landing site, Venus.

Science.gov (United States)

Shellnutt, J Gregory

2018-01-01

Geochemical modeling using the basalt composition analyzed at the Vega 2 landing site indicates that intermediate to silicic liquids can be generated by fractional crystallization and equilibrium partial melting. Fractional crystallization modeling using variable pressures (0.01 GPa to 0.5 GPa) and relative oxidation states (FMQ 0 and FMQ -1) of either a wet (H2O = 0.5 wt%) or dry (H2O = 0 wt%) parental magma can yield silicic (SiO2 > 60 wt%) compositions that are similar to terrestrial ferroan rhyolite. Hydrous (H2O = 0.5 wt%) partial melting can yield intermediate (trachyandesite to andesite) to silicic (trachydacite) compositions at all pressures but requires relatively high temperatures (≥ 950°C) to generate the initial melt at intermediate to low pressure whereas at high pressure (0.5 GPa) the first melts will be generated at much lower temperatures (< 800°C). Anhydrous partial melt modeling yielded mafic (basaltic andesite) and alkaline compositions (trachybasalt) but the temperature required to produce the first liquid is very high (≥ 1130°C). Consequently, anhydrous partial melting is an unlikely process to generate derivative liquids. The modeling results indicate that, under certain conditions, the Vega 2 composition can generate silicic liquids that produce granitic and rhyolitic rocks. The implication is that silicic igneous rocks may form a small but important component of the northeast Aphrodite Terra.

Petrology of the 1995/2000 Magma of Copahue, Argentina

Science.gov (United States)

Goss, A.; Varekamp, J. C.

2001-05-01

Phreatomagmatic eruptions of Copahue in July/August,1995 and July/August 2000 produced mixed juvenile clasts, silica-rich debris from the hydrothermal system, and magmatic scoria with 88 percent SiO2. These high-SiO2 clasts carry an as yet unidentified (crystobalite?), euhedral silica phase in great abundance, which is riddled with tan, primary melt inclusions. The mixed clasts have bands of mafic material with small euhedral olivine, clinopyroxene, and plagioclase that are mixed with an intermediate magma with coarser, resorbed phenocrysts of olivine, plagioclase, clino- and ortho- pyroxene, and rare occurrences of the silica phase. These ejecta are intimate mixtures of a relatively felsic magma similar to Pleistocene Copahue lavas and a mafic basaltic andesite, with minor contributions of a magma contaminated with silica-rich hydrothermal wallrock material. Two-pyroxene geothermometry indicates crystallization temperatures of 1020 deg - 1045 deg C. Glass inclusions (59-63 percent SiO2) in plagioclase and olivine crystals yield very low volatile contents in the melt (0.4-1.5 percent H2O). The 1995/2000 magmas resided at shallow level and degassed into the active volcano-hydrothermal system which discharges acid fluids into the Copahue crater lake and hot springs. More mafic magma intruded this shallow batch and the mixture rose into the hydrothermal system and assimilated siliceous wall rock. A Ti-diffusion profile in a magnetite crystal suggests that the period between magma mixing and eruption was on the order of 4-10 weeks, and the temperature difference between resident and intruding magma was about 50-60 oC.

Numerical modeling of magma-repository interactions

NARCIS (Netherlands)

Bokhove, Onno

2001-01-01

This report explains the numerical programs behind a comprehensive modeling effort of magma-repository interactions. Magma-repository interactions occur when a magma dike with high-volatile content magma ascends through surrounding rock and encounters a tunnel or drift filled with either a magmatic

Sulfur Concentration at Sulfide Saturation in Anhydrous Silicate Melts at Crustal Conditions

Science.gov (United States)

Liu, Y.; Samaha, N.; Baker, D. R.

2006-05-01

The sulfur concentration in silicate melts at sulfide saturation (SCSS) was experimentally investigated in a temperature range from 1250°C to 1450°C and a pressure range from 500 MPa to 1 GPa in a piston-cylinder apparatus. The investigated melt compositions varied from rhyolitic to basaltic. All experiments were saturated with a FeS melt. Temperature was confirmed to have a positive effect on the SCSS and no measurable pressure effect was observed. Oxygen fugacity was controlled to be either near the carbon-carbon monoxide buffer or one log unit above the nickel-nickel oxide buffer, and found to positively affect the SCSS. A series of models were constructed to predict the SCSS as a function of temperature, pressure, melt composition, oxygen fugacity and sulfur fugacity of the system. The coefficients were obtained by the regression of experimental data from this study and from data in the literature. The best model found for the prediction of the SCSS is: ln S (ppm) = 996/T + 9.875 + 0.997 ln MFM + 0.1901 ln fO2 - 0.0722 (P/T) -0.115 ln f S2, where P is in bar, T is in K, and MFM is a compositional parameter describing the melt based upon cation mole fractions: MFM = [Na + K + 2 (Ca + Mg+ Fe2+)]/[Si × (Al + Fe3+)]. This model predicts the SCSS in anhydrous silicate melts from rhyolitic to basaltic compositions at crustal conditions from 1 bar to 1.25 GPa, temperatures from ~1200 to 1400 C, and oxygen fugacities between approximately two log units below the fayalite-quartz-magnetite buffer and one log unit above the nickel-nickel oxide buffer. For cases where the oxygen and sulfur fugacities can not be adequately estimated a simpler model also works acceptably: ln S (ppm) = -5328/T + 8.431 + 1.244 ln MFM - 0.01704(P/T) + ln aFeS, where aFeS is the activity of FeS in the sulfide melt and is well approximated by a value of 1. Additional experiments were performed on other basalts in a temperature range from 1250 C to 1450 C at 1 GPa to test the models. The model

Constraining the Volatile Regime of Primitive Somma-Vesuvius Magmas Based on the Compositions of Phenocrysts and Melt Inclusions

Science.gov (United States)

Danyushevsky, L. V.; Esposito, R.; De Vivo, B.; Redi, D.; Lima, A.; Bodnar, R. J.; Gurenko, A.

2017-12-01

The volcanic complex of Mt. Somma-Vesuvius is located in the Campanian Plain on east of Naples. We present the results of a mineralogical and melt inclusion studies of primitive volcanic products erupted during the last 2 magmatic cycles of Soma-Vesuvius, aimed at better understanding the volatile fluxes and eruptive behaviour of the volcano. Our results suggest that despite large differences in the compositions of the erupted magmas (from olivine-bearing basaltic lavas to leucite-bearing phonolites) and the eruption style (from plinian to strombolian), there was very little change in the nature of the parental magmas. Melt inclusions in olivine phenocrysts in all volcanic products and styles reveal the highest volatile contents in the most magnesian, early formed crystals (Fo90; H2O 4-5 wt%; CO2 3,000-4,000 ppm), decreasing to near 0 levels of concentrations in olivine Fo70. Major and trace element compositions of the clinopyroxene phenocrysts (Mg#92-70) also suggest a similar parental magma composition and similar liquid lines of decent for all Somma-Vesuvius eruptions. Our results are best explained by a model which relates the eruption style to the intensity of melt supply under the volcano. High intensity plinian eruptions occur after a prolonged repose time, whereas strombolian eruptions occur during periods of more frequent volcanic activity [1]. We will also discuss possible implications for the role of carbonate assimilation during magma evolution of Somma-Vesuvius and for total volatile budget of the SOmma-Vesuvius eruptions. [1] [42] Lima, A., Danyushevsky, L.V., De Vivo, B. and Fedele, L. 2003: A model for the evolution of the Mt. Somma-Vesuvius magmatic system based on fluid and melt inclusion investigations. In: Melt Inclusions in volcanic systems: Methods, applications and Problems (B. De Vivo & R.J. Bodnar, Eds), Series: Developments in Volcanology. No. 5 Elsevier, Amsterdam, 227-251

Hydrogen isotopic fractionation during crystallization of the terrestrial magma ocean

Science.gov (United States)

Pahlevan, K.; Karato, S. I.

2016-12-01

Models of the Moon-forming giant impact extensively melt and partially vaporize the silicate Earth and deliver a substantial mass of metal to the Earth's core. The subsequent evolution of the terrestrial magma ocean and overlying vapor atmosphere over the ensuing 105-6 years has been largely constrained by theoretical models with remnant signatures from this epoch proving somewhat elusive. We have calculated equilibrium hydrogen isotopic fractionation between the magma ocean and overlying steam atmosphere to determine the extent to which H isotopes trace the evolution during this epoch. By analogy with the modern silicate Earth, the magma ocean-steam atmosphere system is often assumed to be chemically oxidized (log fO2 QFM) with the dominant atmospheric vapor species taken to be water vapor. However, the terrestrial magma ocean - having held metallic droplets in suspension - may also exhibit a much more reducing character (log fO2 IW) such that equilibration with the overlying atmosphere renders molecular hydrogen the dominant H-bearing vapor species. This variable - the redox state of the magma ocean - has not been explicitly included in prior models of the coupled evolution of the magma ocean-steam atmosphere system. We find that the redox state of the magma ocean influences not only the vapor speciation and liquid-vapor partitioning of hydrogen but also the equilibrium isotopic fractionation during the crystallization epoch. The liquid-vapor isotopic fractionation of H is substantial under reducing conditions and can generate measurable D/H signatures in the crystallization products but is largely muted in an oxidizing magma ocean and steam atmosphere. We couple equilibrium isotopic fractionation with magma ocean crystallization calculations to forward model the behavior of hydrogen isotopes during this epoch and find that the distribution of H isotopes in the silicate Earth immediately following crystallization represents an oxybarometer for the terrestrial

Effect of temperature on hydration kinetics and polymerization of tricalcium silicate in stirred suspensions of CaO-saturated solutions

International Nuclear Information System (INIS)

Grant, Steven A.; Boitnott, Ginger E.; Korhonen, Charles J.; Sletten, Ronald S.

2006-01-01

Tricalcium silicate was hydrated at 274, 278, 283, 298, and 313 K in stirred suspensions of saturated CaO solutions under a nitrogen-gas atmosphere until the end of deceleratory period. The suspension conductivities and energy flows were measured continuously. The individual reaction rates for tricalcium silicate dissolution, calcium silicate hydrate precipitation, and calcium hydroxide precipitation were calculated from these measurements. The results suggest that the proportion of tricalcium silicate dissolved was determined by the rate of tricalcium silicate dissolution and the time to very rapid calcium hydroxide precipitation. The time to very rapid calcium hydroxide precipitation was more sensitive to changes in temperature than was the rate of tricalcium silicate dissolution, so that the proportion of tricalcium silicate hydration dissolved by the deceleratory period increased with decreasing temperature. The average chain length of the calcium silicate hydrate ascertained by magic-angle spinning nuclear magnetic resonance spectroscopy increased with increasing temperature

Mantle to surface degassing of carbon- and sulphur-rich alkaline magma at El Hierro, Canary Islands

Science.gov (United States)

Longpré, Marc-Antoine; Stix, John; Klügel, Andreas; Shimizu, Nobumichi

2017-02-01

Basaltic volcanoes transfer volatiles from the mantle to the surface of the Earth. The quantification of deep volatile fluxes relies heavily on estimates of the volatile content of primitive magmas, the best archive of which is provided by melt inclusions. Available data from volcanoes producing mafic alkaline lavas in a range of tectonic settings suggest high volatile fluxes, but information remains sparse, particularly for intraplate ocean islands. Here we present measurements of volatile and trace element concentrations, as well as sulphur speciation, in olivine-hosted melt inclusions and matrix glasses from quenched basanite lava balloon samples from the 2011-2012 submarine eruption at El Hierro, Canary Islands. The results reveal remarkably high concentrations of dissolved volatiles and incompatible trace elements in this magma, with ∼80 ppm Nb and up to 3420 ppm CO2, 3.0 wt.% H2O and 5080 ppm S. Reconstructed primitive CO2 contents, considering CO2/Nb systematics and possible CO2 sequestration in shrinkage bubbles, reach weight percent levels, indicating that carbon is a major constituent of Canary Island magmas at depth and that exsolution of a CO2-rich fluid begins in the mantle at pressures in excess of 1 GPa. Correlations between sulphur concentration, sulphur speciation and water content suggest strong reduction of an initially oxidised mantle magma, likely controlled by coupled H2O and S degassing. This late-stage redox change may have triggered sulphide saturation, recorded by globular sulphide inclusions in clinopyroxene and ulvöspinel. The El Hierro basanite thus had a particularly high volatile-carrying capacity and released a minimum of 1.3-2.1 Tg CO2 and 1.8-2.9 Tg S to the environment, causing substantial stress on the local submarine ecosystem. These results highlight the important contribution of alkaline ocean island volcanoes, such as the Canary Islands, to volatile fluxes from the mantle.

Dynamic observations of vesiculation reveal the role of silicate crystals in bubble nucleation and growth in andesitic magmas

Energy Technology Data Exchange (ETDEWEB)

Pleše, P.; Higgins, M. D.; Mancini, L.; Lanzafame, G.; Brun, F.; Fife, J. L.; Casselman, J.; Baker, D. R.

2018-01-01

Bubble nucleation and growth control the explosivity of volcanic eruptions, and the kinetics of these processes are generally determined from examinations of natural samples and quenched experimental run products. These samples, however, only provide a view of the final state, from which the initial conditions of a time-evolving magmatic system are then inferred. The interpretations that follow are inexact due to the inability of determining the exact conditions of nucleation and the potential detachment of bubbles from their nucleation sites, an uncertainty that can obscure their nucleation location – either homogeneously within the melt or heterogeneously at the interface between crystals and melts. We present results of a series of dynamic, real-time 4D X-ray tomographic microscopy experiments where we observed the development of bubbles in crystal bearing silicate magmas. Experimentally synthesized andesitic glasses with 0.25–0.5 wt% H2O and seed silicate crystals were heated at 1 atm to induce bubble nucleation and track bubble growth and movement. In contrast to previous studies on natural and experimentally produced samples, we found that bubbles readily nucleated on plagioclase and clinopyroxene crystals, that their contact angle changes during growth and that they can grow to sizes many times that of the silicate on whose surface they originated. The rapid heterogeneous nucleation of bubbles at low degrees of supersaturation in the presence of silicate crystals demonstrates that silicates can affect when vesiculation ensues, influencing subsequent permeability development and effusive vs. explosive transition in volcanic eruptions.

Dynamic observations of vesiculation reveal the role of silicate crystals in bubble nucleation and growth in andesitic magmas

Science.gov (United States)

Pleše, P.; Higgins, M. D.; Mancini, L.; Lanzafame, G.; Brun, F.; Fife, J. L.; Casselman, J.; Baker, D. R.

2018-01-01

Bubble nucleation and growth control the explosivity of volcanic eruptions, and the kinetics of these processes are generally determined from examinations of natural samples and quenched experimental run products. These samples, however, only provide a view of the final state, from which the initial conditions of a time-evolving magmatic system are then inferred. The interpretations that follow are inexact due to the inability of determining the exact conditions of nucleation and the potential detachment of bubbles from their nucleation sites, an uncertainty that can obscure their nucleation location - either homogeneously within the melt or heterogeneously at the interface between crystals and melts. We present results of a series of dynamic, real-time 4D X-ray tomographic microscopy experiments where we observed the development of bubbles in crystal bearing silicate magmas. Experimentally synthesized andesitic glasses with 0.25-0.5 wt% H2O and seed silicate crystals were heated at 1 atm to induce bubble nucleation and track bubble growth and movement. In contrast to previous studies on natural and experimentally produced samples, we found that bubbles readily nucleated on plagioclase and clinopyroxene crystals, that their contact angle changes during growth and that they can grow to sizes many times that of the silicate on whose surface they originated. The rapid heterogeneous nucleation of bubbles at low degrees of supersaturation in the presence of silicate crystals demonstrates that silicates can affect when vesiculation ensues, influencing subsequent permeability development and effusive vs. explosive transition in volcanic eruptions.

The mechanics of shallow magma reservoir outgassing

Science.gov (United States)

Parmigiani, A.; Degruyter, W.; Leclaire, S.; Huber, C.; Bachmann, O.

2017-08-01

Magma degassing fundamentally controls the Earth's volatile cycles. The large amount of gas expelled into the atmosphere during volcanic eruptions (i.e., volcanic outgassing) is the most obvious display of magmatic volatile release. However, owing to the large intrusive:extrusive ratio, and considering the paucity of volatiles left in intrusive rocks after final solidification, volcanic outgassing likely constitutes only a small fraction of the overall mass of magmatic volatiles released to the Earth's surface. Therefore, as most magmas stall on their way to the surface, outgassing of uneruptible, crystal-rich magma storage regions will play a dominant role in closing the balance of volatile element cycling between the mantle and the surface. We use a numerical approach to study the migration of a magmatic volatile phase (MVP) in crystal-rich magma bodies ("mush zones") at the pore scale. Our results suggest that buoyancy-driven outgassing is efficient over crystal volume fractions between 0.4 and 0.7 (for mm-sized crystals). We parameterize our pore-scale results for MVP migration in a thermomechanical magma reservoir model to study outgassing under dynamical conditions where cooling controls the evolution of the proportion of crystal, gas, and melt phases and to investigate the role of the reservoir size and the temperature-dependent viscoelastic response of the crust on outgassing efficiency. We find that buoyancy-driven outgassing allows for a maximum of 40-50% volatiles to leave the reservoir over the 0.4-0.7 crystal volume fractions, implying that a significant amount of outgassing must occur at high crystal content (>0.7) through veining and/or capillary fracturing.

Zircon crytallization and recycling in the magma chamber of the rhyolitic Kos Plateau Tuff (Aegean arc)

Science.gov (United States)

Bachman, O.; Charlier, B.L.A.; Lowenstern, J. B.

2007-01-01

In contrast to most large-volume silicic magmas in continental arcs, which are thought to evolve as open systems with significant assimilation of preexisting crust, the Kos Plateau Miff magma formed dominantly by crystal fractionation of mafic parents. Deposits from this ??? 60 km3 pyroclastic eruption (the largest known in the Aegean arc) lack xenocrystic zircons [secondary ion mass spectrometry (SIMS) U-Pb ages on zircon cores never older than 500 ka] and display Sr-Nd whole-rock isotopic ratios within the range of European mantle in an area with exposed Paleozoic and Tertiary continental crust; this evidence implies a nearly closed-system chemical differentiation. Consequently, the age range provided by zircon SIMS U-Th-Pb dating is a reliable indicator of the duration of assembly and longevity of the silicic magma body above its solidus. The age distribution from 160 ka (age of eruption by sanidine 40Ar/39Ar dating; Smith et al., 1996) to ca. 500 ka combined with textural characteristics (high crystal content, corrosion of most anhydrous phenocrysts, but stability of hydrous phases) suggest (1) a protracted residence in the crust as a crystal mush and (2) rejuvenation (reduced crystallization and even partial resorption of minerals) prior to eruption probably induced by new influx of heat (and volatiles). This extended evolution chemically isolated from the surrounding crust is a likely consequence of the regional geodynamics because the thinned Aegean microplate acts as a refractory container for magmas in the dying Aegean subduction zone (continent-continent subduction). ?? 2007 Geological Society of America.

Zircon crystallization and recycling in the magma chamber of the rhyolitic Kos Plateau Tuff (Aegean arc)

Science.gov (United States)

Bachman, O.; Charlier, B.L.A.; Lowenstern, J. B.

2007-01-01

In contrast to most large-volume silicic magmas in continental arcs, which are thought to evolve as open systems with significant assimilation of preexisting crust, the Kos Plateau Tuff magma formed dominantly by crystal fractionation of mafic parents. Deposits from this ~60 km3 pyroclastic eruption (the largest known in the Aegean arc) lack xenocrystic zircons [secondary ion mass spectrometry (SIMS) U-Pb ages on zircon cores never older than 500 ka] and display Sr-Nd whole-rock isotopic ratios within the range of European mantle in an area with exposed Paleozoic and Tertiary continental crust; this evidence implies a nearly closed-system chemical differentiation. Consequently, the age range provided by zircon SIMS U-Th-Pb dating is a reliable indicator of the duration of assembly and longevity of the silicic magma body above its solidus. The age distribution from 160 ka (age of eruption by sanidine 40Ar/39Ar dating; Smith et al., 1996) to ca. 500 ka combined with textural characteristics (high crystal content, corrosion of most anhydrous phenocrysts, but stability of hydrous phases) suggest (1) a protracted residence in the crust as a crystal mush and (2) rejuvenation (reduced crystallization and even partial resorption of minerals) prior to eruption probably induced by new influx of heat (and volatiles). This extended evolution chemically isolated from the surrounding crust is a likely consequence of the regional geodynamics because the thinned Aegean microplate acts as a refractory container for magmas in the dying Aegean subduction zone (continent-continent subduction).

Eruptive dynamics during magma decompression: a laboratory approach

Science.gov (United States)

Spina, L.; Cimarelli, C.; Scheu, B.; Wadsworth, F.; Dingwell, D. B.

2013-12-01

A variety of eruptive styles characterizes the activity of a given volcano. Indeed, eruptive styles can range from effusive phenomena to explosive eruptions, with related implications for hazard management. Rapid changes in eruptive style can occur during an ongoing eruption. These changes are, amongst other, related to variations in the magma ascent rate, a key parameter affecting the eruptive style. Ascent rate is in turn dependent on several factors such as the pressure in the magma chamber, the physical properties of the magma and the rate at which these properties change. According to the high number of involved parameters, laboratory decompression experiments are the best way to achieve quantitative information on the interplay of each of those factors and the related impact on the eruption style, i.e. by analyzing the flow and deformation behavior of the transparent volatile-bearing analogue fluid. We carried out decompression experiments following different decompression paths and using silicone oil as an analogue for the melt, with which we can simulate a range of melt viscosity values. For a set of experiments we added rigid particles to simulate the presence of crystals in the magma. The pure liquid or suspension was mounted into a transparent autoclave and pressurized to different final pressures. Then the sample was saturated with argon for a fixed amount of time. The decompression path consists of a slow decompression from the initial pressure to the atmospheric condition. Alternatively, samples were decompressed almost instantaneously, after established steps of slow decompression. The decompression path was monitored with pressure transducers and a high-speed video camera. Image analysis of the videos gives quantitative information on the bubble distribution with respect to depth in the liquid, pressure and time of nucleation and on their characteristics and behavior during the ongoing magma ascent. Furthermore, we also monitored the evolution of

The origin and evolution of silicic magmas during continental rifting: new constraints from trace elements and oxygen isotopes from Ethiopian volcanoes

Science.gov (United States)

Hutchison, W.; Boyce, A.; Mather, T. A.; Pyle, D. M.; Yirgu, G.; Gleeson, M. L.

2017-12-01

The petrologic diversity of rift magmas is generated by two key processes: interaction with the crust via partial melting or assimilation; and closed-system fractional crystallization of the parental magma. It is not yet known whether these two petrogenetic processes vary spatially between different rift settings, and whether there are any significant secular variations during rift evolution. The Ethiopian Rift is the ideal setting to test these hypotheses because it captures the transition from continental rifting to sea-floor spreading and has witnessed the eruption of large volumes of mafic and silicic volcanic rocks since 30 Ma. We use new oxygen isotope (δ18O) and trace element data to fingerprint fractional crystallisation and partial crustal melting processes in Ethiopia and evaluate spatial variations between three active rift segments. δ18O measurements are used to examine partial crustal melting processes. We find that most δ18O data from basalts to rhyolites fall within the bounds of modelled fractional crystallization trajectories (i.e., 5.5-6.5 ‰). Few samples deviate from this trend, emphasising that fractional crystallization is the dominant petrogenetic processes and that little fusible Precambrian crustal material (δ18O of 7-18 ‰) remain to be assimilated beneath the magmatic segments. Trace element systematics (e.g., Ba, Sr, Rb, Th and Zr) further underscore the dominant role of fractional crystallization but also reveal important variations in the degree of melt evolution between the volcanic systems. We find that the most evolved silicic magmas, i.e., those with greatest peralkalinity (molar Na2O+K2O>Al2O3), are promoted in regions of lowest magma flux off-axis and along rift. Our findings provide new information on the nature of the crust beneath Ethiopia's active magmatic segments and also have relevance for understanding ancient rift zones and the geotectonic settings that promote genesis of economically-valuable mineral deposits.

The Effect of Pressure on Iron Speciation in Silicate Melts at a Fixed Oxygen Fugacity: The Possibility of a Redox Profile Through a Terrestrial Magma Ocean

Science.gov (United States)

Armstrong, K.; Frost, D. J.; McCammon, C. A.; Rubie, D. C.; Boffa Ballaran, T.

2017-12-01

As terrestrial planets accreted, mantle silicates equilibrated with core-forming metallic iron, which would have imposed a mantle oxygen fugacity below the iron-wüstite oxygen buffer. Throughout Earth's history, however, the oxygen fugacity of at least the accessible portions of the upper mantle has been 4-5 orders of magnitude higher. The process that caused the rapid increase in the redox state of the mantle soon after core formation is unclear. Here we test the possibility that pressure stabilises ferric iron in silicate melts, as has been observed in silicate minerals. A deep magma ocean, which would have likely existed towards the end of accretion, could then develop a gradient in oxygen fugacity for a fixed ferric-ferrous ratio as a result of pressure. We have equilibrated an andesitic melt with a Ru-RuO2 buffer in a multianvil press between 5 and 24 GPa. Further experiments were performed on the same melt in equilibrium with iron metal. The recovered melts were then analysed using Mössbauer spectroscopy to determine the ferric/ferrous ratio. The results show that for the Ru-RuO2 buffer at lower pressures, the ferric iron content decreases with pressure, due to a positive volume change of the reaction FeO + 1/4O2 = FeO1.5. Ferric iron content also appears to be sensitive to water content at lower pressures. However, above 15 GPa this trend apparently reverses and the ferric iron content increases with pressure. This reversal in pressure dependence would drive the oxygen fugacity of a deep magma ocean with a fixed ferric/ferrous ratio down with increasing depth. This would create a redox gradient, where the magma ocean could potentially be in equilibrium with metallic iron at its base but more oxidised in its shallower regions. Crystallisation of this magma ocean could render an upper mantle oxygen fugacity similar to that in the Earth's accessible mantle today.

Influence of volatile degassing on the eruptibility of large igneous province magmatic systems

Science.gov (United States)

Mittal, T.; Richards, M. A.

2017-12-01

Magmatic volatiles, in particular their buoyancy, may play a critical role in determining whether a magma reservoir can build up enough overpressure leading to drive flood basalt eruptions (Black & Manga 2017). Thus, it is important to understand the extent to which volatiles can remain trapped in a magmatic system and how they influence the eruptibility. Although the high-temperature metamorphic aureloe around a magma chamber is typically considered to have low permeability due to ductile creep, recent theoretical, experimental, and field work (e.g. Noriaki et al. 2017) have highlighted the role of dynamic permeability in magmatic systems. Consequently, the effective permeability of the crust when magma is present in the system can be orders of magnitude larger than that of exhumed rock samples. We model dynamic permeability changes as a competition between hydro-fracturing (increased porosity) and fracture closure by ductile creep and hydrothermal mineral precipitation (reduced porosity) and find yearly-to-decadal time-scales for periodic fracturing and fluid loss events and an increase in average permeability. We then use a fully coupled poro-thermo-elastic framework to model to explore the macroscopic influence of volatile loss on the stress state of the crust in this higher time-averaged permeability setting. We derive new semi-analytical solutions and combine them with a magma chamber box model (modified from Degruyter & Huber 2014) to analyze system-scale dynamics for both basaltic and silicic magmatic systems. We find that passive degassing likely has a substantial temporal influence on the stress distribution in the crust and the highly crystalline mush zone immediately surrounding a magma reservoir, and find an additional scale : pore-pressure diffusion timescale that exerts a first-order control on the magnitude and frequency of volcanic eruptions. We also explore how disconnected magma batches interact indirectly with each other and its implications for

Lattice thermal conductivity of silicate glasses at high pressures

Science.gov (United States)

Chang, Y. Y.; Hsieh, W. P.

2016-12-01

Knowledge of the thermodynamic and transport properties of magma holds the key to understanding the thermal evolution and chemical differentiation of Earth. The discovery of the remnant of a deep magma ocean above the core mantle boundary (CMB) from seismic observations suggest that the CMB heat flux would strongly depend on the thermal conductivity, including lattice (klat) and radiative (krad) components, of dense silicate melts and major constituent minerals around the region. Recent measurements on the krad of dense silicate glasses and lower-mantle minerals show that krad of dense silicate glasses could be significantly smaller than krad of the surrounding solid mantle phases, and therefore the dense silicate melts would act as a thermal insulator in deep lower mantle. This conclusion, however, remains uncertain due to the lack of direct measurements on the lattice thermal conductivity of silicate melts under relevant pressure-temperature conditions. Besides the CMB, magmas exist in different circumstances beneath the surface of the Earth. Chemical compositions of silicate melts vary with geological and geodynamic settings of the melts and have strong influences on their thermal properties. In order to have a better view of heat transport within the Earth, it is important to study compositional and pressure dependences of thermal properties of silicate melts. Here we report experimental results on lattice thermal conductivities of silicate glasses with basaltic and rhyolitic compositions up to Earth's lower mantle pressures using time-domain thermoreflectance coupled with diamond-anvil cell techniques. This study not only provides new data for the thermal conductivity of silicate melts in the Earth's deep interior, but is crucial for further understanding of the evolution of Earth's complex internal structure.

Volcanic emission of radionuclides and magma dynamics

International Nuclear Information System (INIS)

Lambert, G.; Le Cloarec, M.F.; Ardouin, B.; Le Roulley, J.C.

1985-01-01

210 Pb, 210 Bi and 210 Po, the last decay products of the 238 U series, are highly enriched in volcanic plumes, relative to the magma composition. Moreover this enrichment varies over time and from volcano to volcano. A model is proposed to describe 8 years of measurements of Mt. Etna gaseous emissions. The lead and bismuth coefficients of partition between gaseous and condensated phases in the magma are determined by comparing their concentrations in lava flows and condensated volatiles. In the case of volatile radionuclides, an escaping time is calculated which appears to be related to the volcanic activity. Finally, it is shown that that magma which is degassing can already be partly degassed; it should be considered as a mixture of a few to 50% of deep non-degassed magma with a well degassed superficial magma cell. (orig.)

The Evidence from Inclusions in Pumices for the Direct Degassing of Volatiles from the Magma to the Hydrothermal Fluids in the Okinawa Trough

Institute of Scientific and Technical Information of China (English)

YU Zenghui; ZHAI Shikui; ZHAO Guangtao

2002-01-01

This article presents the evidence in support of the direct magma degassing as the principal mechanism of volatilesreleasing into the hydrothermal fluids in the Okinawa Trough, as contrasted to the argument for the hydrothermal strippingof volatiles from the volcanic rocks.Laser Raman microprobe and stepped-heating techniques are employed to determine the compositions and contents of thevolatiles in pumices in the middle Okinawa Trough. The results show that the volatiles are similar to the gases in the hy-drothermal fluids and hydrothermal minerals in composition, the mean percent content of each component and variationtrend. This indicates the direct influence of magma degassing on the hydrothermal fluids. In addition, the contents ofvolatiles in pumices are rather low and do not support the hydrothermal stripping as the main mechanism to enrich the fluidswith gases. The results are consistent with the idea that the direct magma degassing is more important than hydrothermalstripping in supplying gases to the hydrothermal fluids in the Okinawa Trough.

Decadal to monthly timescales of magma transfer and reservoir growth at a caldera volcano.

Science.gov (United States)

Druitt, T H; Costa, F; Deloule, E; Dungan, M; Scaillet, B

2012-02-01

Caldera-forming volcanic eruptions are low-frequency, high-impact events capable of discharging tens to thousands of cubic kilometres of magma explosively on timescales of hours to days, with devastating effects on local and global scales. Because no such eruption has been monitored during its long build-up phase, the precursor phenomena are not well understood. Geophysical signals obtained during recent episodes of unrest at calderas such as Yellowstone, USA, and Campi Flegrei, Italy, are difficult to interpret, and the conditions necessary for large eruptions are poorly constrained. Here we present a study of pre-eruptive magmatic processes and their timescales using chemically zoned crystals from the 'Minoan' caldera-forming eruption of Santorini volcano, Greece, which occurred in the late 1600s BC. The results provide insights into how rapidly large silicic systems may pass from a quiescent state to one on the edge of eruption. Despite the large volume of erupted magma (40-60 cubic kilometres), and the 18,000-year gestation period between the Minoan eruption and the previous major eruption, most crystals in the Minoan magma record processes that occurred less than about 100 years before the eruption. Recharge of the magma reservoir by large volumes of silicic magma (and some mafic magma) occurred during the century before eruption, and mixing between different silicic magma batches was still taking place during the final months. Final assembly of large silicic magma reservoirs may occur on timescales that are geologically very short by comparison with the preceding repose period, with major growth phases immediately before eruption. These observations have implications for the monitoring of long-dormant, but potentially active, caldera systems.

Artificial magma program: Report on workshop held in Oak Ridge, Tennessee on March 29-30, 1994

International Nuclear Information System (INIS)

Naney, M.T.; Jacobs, G.K.

1995-03-01

A workshop was organized and conducted in Oak Ridge, Tennessee, on March 29 and 30, 1994, to evaluate the use of in situ vitrification (ISV) technology to produce large silicate melts that would serve as analogs for natural magmas for the study of magmatic properties and processes. ISV technology would permit experiments to test hypotheses or provide new data that cannot be tested or obtained through bench-top experimentation or the study of natural systems. The scale of ISV melts is intermediate between that of natural lava lakes and laboratory crucible experiments, with melt volumes from 15 to 300 m 3 easily obtained. This approach permits investigation of dynamic processes which operate on scales difficult to simulate through bench-top experimentation and that are not amenable to direct observation or control in natural systems (e.g., degassing, convection, and crystal settling). Several aspects of the ISV process make it uniquely applicable for the study of magma systems. The process produces open-quotes containerlessclose quotes silicate melts, which permits development of important analog components of natural magma systems including: partial melt zones, stopping, contact metamorphic haloes, and open-quotes hydrothermalclose quotes fluids. The lack of a melt open-quotes containerclose quotes also enables use of standard field-scale geophysical instrumentation for studying the seismic and electrical properties of the melt and host materials. In addition, volatile and particulate emissions from the melt can be sampled using methods that avoid reaction with, and contamination by, host rocks. The consensus of the group was that the use of melts generated by ISV technology provided unique opportunities to advance the understanding of magmas and magmatic processes and warranted development of a proposal

Sphene and zircon in the Highland Range volcanic sequence (Miocene, southern Nevada, USA): Elemental partitioning, phase relations, and influence on evolution of silicic magma

Science.gov (United States)

Colombini, L.L.; Miller, C.F.; Gualda, G.A.R.; Wooden, J.L.; Miller, J.S.

2011-01-01

Sphene is prominent in Miocene plutonic rocks ranging from diorite to granite in southern Nevada, USA, but it is restricted to rhyolites in coeval volcanic sequences. In the Highland Range volcanic sequence, sphene appears as a phenocryst only in the most evolved rocks (72-77 mass% SiO2; matrix glass 77-78 mass% SiO2). Zr-in-sphene temperatures of crystallization are mostly restricted to 715 and 755??C, in contrast to zircon (710-920??C, Ti-in-zircon thermometry). Sphene rim/glass Kds for rare earth elements are extremely high (La 120, Sm 1200, Gd 1300, Lu 240). Rare earth elements, especially the middle REE (MREE), decrease from centers to rims of sphene phenocrysts along with Zr, demonstrating the effect of progressive sphene fractionation. Whole rocks and glasses have MREE-depleted, U-shaped REE patterns as a consequence of sphene fractionation. Within the co-genetic, sphene-rich Searchlight pluton, only evolved leucogranites show comparable MREE depletion. These results indicate that sphene saturation in intruded and extruded magmas occurred only in highly evolved melts: abundant sphene in less silicic plutonic rocks represents a late-stage 'bloom' in fractionated interstitial melt. ?? 2011 Springer-Verlag.

Platinum-group element geochemistry used to determine Cu and Au fertility in the Northparkes igneous suites, New South Wales, Australia

Science.gov (United States)

Hao, Hongda; Campbell, Ian H.; Park, Jung-Woo; Cooke, David R.

2017-11-01

Recent studies have shown that platinum-group elements (PGE) can be used to constrain the timing of sulfide saturation in evolving felsic systems. In this study, we report trace-element, PGE, Re and Au data for the barren and ore-associated suites of intermediate to felsic rocks from the Northparkes Cu-Au porphyry region, emphasizing the timing of sulfide saturation and its influence on the tenor of the associated hydrothermal mineralization. Two barren suites, the Goonumbla and Wombin Volcanics and associate intrusive rocks, are found in the region. Geochemical modelling shows that the barren suites are dominated by plagioclase-pyroxene fractionation, whereas the ore-associated Northparkes Cu-Au porphyry suite is characterized by plagioclase-amphibole fractionation, which requires the ore-bearing suite to have crystallized from a wetter magma than barren suites. The concentrations of PGE, Re and Au in the barren suites decrease continuously during fractional crystallization. This is attributed to early sulfide saturation with the fraction of immiscible sulfide precipitation required to produce the observed trend, being 0.13 and 0.16 wt.% for the Goonumbla and Wombin suites, respectively. The calculated partition coefficients for Au and Pd required to model the observed change in these elements with MgO are well below published values, indicating that R, the mass ratio of silicate to sulfide melt, played a significant role in controlling the rate of decline of these elements with fractionation. Palladium in the ore-associated suite, in contrast, first increases with fractionation then decreases abruptly at 1.2 wt.% MgO. The sharp decrease is attributed to the onset of sulfide precipitation. Platinum on the other hand shows a moderate decrease, starting from the highest MgO sample analysed, but then decreasing strongly from 1.2 wt.% MgO. The initial Pt decrease is attributed to precipitation of a platinum-group mineral (PGM), probably a Pt-Fe alloy, and the sharp

Intrusion of basaltic magma into a crystallizing granitic magma chamber: The Cordillera del Paine pluton in southern Chile

Science.gov (United States)

Michael, Peter J.

1991-10-01

, sodic plagioclase, mica and quartz. The early formed gabbroic minerals (and their coronas) are very similar to phenocrysts in late basaltic dikes that cut the upper levels of the CP granite. The inferred parental magmas of both dikes and gabbros were very similar to subalkaline basalts of the Patagonian Plateau that erupted at about the same time, 35 km to the east. Mafic and silicic magmas at Cordillera del Paine are consanguineous, as demonstrated by alkalinity and trace-element ratios. However, the contemporaneity of mafic and silicic magmas precludes a parent-daughter relationship. The granitic magma most likely was derived by differentiation of mafic magmas that were similar to those that later intruded it. Or, the granitic magma may have been contaminated by mafic magmas similar to the PMC magmas before its shallow emplacement. Mixing would be favored at deeper levels when the cooling rate was lower and the granitic magma was less solidified.

Magma Expansion and Fragmentation in a Propagating Dike (Invited)

Science.gov (United States)

Jaupart, C. P.; Taisne, B.

2010-12-01

The influence of magma expansion due to volatile exsolution and gas dilation on dike propagation is studied using a new numerical code. Many natural magmas contain sufficient amounts of volatiles for fragmentation to occur well below Earth's surface. Magma fragmentation has been studied for volcanic flows through open conduits but it should also occur within dikes that rise towards Earth's surface. We consider the flow of a volatile-rich magma in a hydraulic fracture. The mixture of melt and gas is treated as a compressible viscous fluid below the fragmentation level and as a gas phase carrying melt droplets above it. A numerical code solves for elastic deformation of host rocks, the flow of the magmatic mixture and fracturing at the dike tip. With volatile-free magma, a dike fed at a constant rate in a uniform medium adopts a constant shape and width and rises at a constant velocity. With volatiles involved, magma expands and hence the volume flux of magma increases. With no fragmentation, this enhanced flux leads to acceleration of the dike. Simple scaling laws allow accurate predictions of dike width and ascent rate for a wide range of conditions. With fragmentation, dike behavior is markedly different. Due to the sharp drop of head loss that occurs in gas-rich fragmented material, large internal overpressures develop below the tip and induce swelling of the nose region, leading to deceleration of the dike. Thus, the paradoxical result is that, with no viscous impediment on magma flow and a large buoyancy force, the dike stalls. This process may account for some of the tuffisite veins and intrusions that are found in and around magma conduits, notably in the Unzen drillhole, Japan. We apply these results to the two-month long period of volcanic unrest that preceded the May 1980 eruption of Mount St Helens. An initial phase of rapid earthquake migration from the 7-8 km deep reservoir to shallow levels was followed by very slow progression of magma within the

Influence of extrusion rate and magma rheology on the growth of lava domes: Insights from particle-dynamics modeling

Science.gov (United States)

Husain, Taha; Elsworth, Derek; Voight, Barry; Mattioli, Glen; Jansma, Pamela

2014-09-01

Lava domes are structures that grow by the extrusion of viscous silicic or intermediate composition magma from a central volcanic conduit. Repeated cycles of growth are punctuated by collapse, as the structure becomes oversized for the strength of the composite magma that rheologically stiffens and strengthens at its surface. Here we explore lava dome growth and failure mechanics using a two-dimensional particle-dynamics model. The model follows the evolution of fractured lava, with solidification driven by degassing induced crystallization of magma. The particle-dynamics model emulates the natural development of dome growth and rearrangement of the lava dome which is difficult in mesh-based analyses due to mesh entanglement effects. The deformable talus evolves naturally as a frictional carapace that caps a ductile magma core. Extrusion rate and magma rheology together with crystallization temperature and volatile content govern the distribution of strength in the composite structure. This new model is calibrated against existing observational models of lava dome growth. Results show that the shape and extent of the ductile core and the overall structure of the lava dome are strongly controlled by the infusion rate. The effects of extrusion rate on magma rheology are sensitive to material stiffness, which in turn is a function of volatile content and crystallinity. Material stiffness and material strength are key model parameters which govern magma rheology and subsequently the morphological character of the lava dome and in turn stability. Degassing induced crystallization causes material stiffening and enhances material strength reflected in non-Newtonian magma behavior. The increase in stiffness and strength of the injected magma causes a transition in the style of dome growth, from endogenous expansion of a ductile core, to stiffer and stronger intruding material capable of punching through the overlying material and resulting in the development of a spine or

Segregating gas from melt: an experimental study of the Ostwald ripening of vapor bubbles in magmas

Science.gov (United States)

Lautze, Nicole C.; Sisson, Thomas W.; Mangan, Margaret T.; Grove, Timothy L.

2011-01-01

Diffusive coarsening (Ostwald ripening) of H2O and H2O-CO2 bubbles in rhyolite and basaltic andesite melts was studied with elevated temperature–pressure experiments to investigate the rates and time spans over which vapor bubbles may enlarge and attain sufficient buoyancy to segregate in magmatic systems. Bubble growth and segregation are also considered in terms of classical steady-state and transient (non-steady-state) ripening theory. Experimental results are consistent with diffusive coarsening as the dominant mechanism of bubble growth. Ripening is faster in experiments saturated with pure H2O than in those with a CO2-rich mixed vapor probably due to faster diffusion of H2O than CO2 through the melt. None of the experimental series followed the time1/3 increase in mean bubble radius and time-1 decrease in bubble number density predicted by classical steady-state ripening theory. Instead, products are interpreted as resulting from transient regime ripening. Application of transient regime theory suggests that bubbly magmas may require from days to 100 years to reach steady-state ripening conditions. Experimental results, as well as theory for steady-state ripening of bubbles that are immobile or undergoing buoyant ascent, indicate that diffusive coarsening efficiently eliminates micron-sized bubbles and would produce mm-sized bubbles in 102–104 years in crustal magma bodies. Once bubbles attain mm-sizes, their calculated ascent rates are sufficient that they could transit multiple kilometers over hundreds to thousands of years through mafic and silicic melt, respectively. These results show that diffusive coarsening can facilitate transfer of volatiles through, and from, magmatic systems by creating bubbles sufficiently large for rapid ascent.

Temperature dependence of sulfide and sulfate solubility in olivine-saturated basaltic magmas

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Beermann, O.; Botcharnikov, R. E.; Holtz, F.; Diedrich, O.; Nowak, M.

2011-12-01

The sulfur concentration at pyrrhotite- and anhydrite-saturation in primitive hydrous basaltic melt of the 2001-2002 eruption of Mt. Etna was determined at 200 MPa, T = 1050-1250 °C and at log fO 2 from FMQ to FMQ+2.2 (FMQ is Fayalite-Magnetite-Quartz oxygen buffer). At 1050 °C Au sample containers were used. A double-capsule technique, using a single crystal olivine sample container closed with an olivine piston, embedded in a sealed Au 80Pd 20 capsule, was developed to perform experiments in S-bearing hydrous basaltic systems at T > 1050 °C. Pyrrhotite is found to be a stable phase coexisting with melt at FMQ-FMQ+0.3, whereas anhydrite is stable at FMQ+1.4-FMQ+2.2. The S concentration in the melt increases almost linearly from 0.12 ± 0.01 to 0.39 ± 0.02 wt.% S at FeS-saturation and from 0.74 ± 0.01 to 1.08 ± 0.04 wt.% S at anhydrite-saturation with T ranging from 1050-1250 °C. The relationships between S concentration at pyrrhotite and/or anhydrite saturation, MgO content of the olivine-saturated melt, T, and log fO 2 observed in this study and from previous data are used to develop an empirical model for estimating the magmatic T and fO 2 from the S and MgO concentrations of H 2O-bearing olivine-saturated basaltic melts. The model can also be used to determine maximum S concentrations, if fO 2 and MgO content of the melt are known. The application of the model to compositions of melt inclusions in olivines from Mt. Etna indicates that the most primitive magmas trapped in inclusions might have been stored at log fO 2 slightly higher than FMQ+1 and at T = 1100-1150 °C, whereas more evolved melts could have been trapped at T ⩽ 1100 °C. These values are in a good agreement with the estimates obtained by other independent methods reported in the literature.

Magma wagging and whirling in volcanic conduits

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Liao, Yang; Bercovici, David; Jellinek, Mark

2018-02-01

Seismic tremor characterized by 0.5-7 Hz ground oscillations commonly occur before and during eruptions at silicic volcanoes with widely ranging vent geometries and edifice structures. The ubiquitous characteristics of this tremor imply that its causes are potentially common to silicic volcanoes. Here we revisit and extend to three dimensions the magma-wagging model for tremor (Jellinek and Bercovici, 2011; Bercovici et al., 2013), wherein a stiff magma column rising in a vertical conduit oscillates against a surrounding foamy annulus of bubbly magma, giving rise to tremor. While prior studies were restricted to two-dimensional lateral oscillations, here we explore three-dimensional motion and additional modes of oscillations. In the absence of viscous damping, the magma column undergoes 'whirling' motion: the center of each horizontal section of the column traces an elliptical trajectory. In the presence of viscous effect we identify new 'coiling' and 'uncoiling' column bending shapes with relatively higher and comparable rates of dissipation to the original two-dimensional magma wagging model. We also calculate the seismic P-wave response of the crustal material around the volcanic conduit to the new whirling motions and propose seismic diagnostics for different wagging patterns using the time-lag between seismic stations. We test our model by analyzing pre-eruptive seismic data from the 2009 eruption of Redoubt Volcano. In addition to suggesting that the occurrence of elliptical whirling motion more than 1 week before the eruption, our analysis of seismic time-lags also implies that the 2009 eruption was accompanied by qualitative changes in the magma wagging behavior including fluctuations in eccentricity and a reversal in the direction of elliptical whirling motion when the eruption was immediately impending.

Chlorine as a geobarometer tool: Application to the explosive eruptions of the Volcanic Campanian District (Mount Somma-Vesuvius, Phlegrean Fields, Ischia)

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Balcone-Boissard, Hélène; Boudon, Georges; Zdanowicz, Géraldine; Orsi, Giovanni; Civetta, Lucia; Webster, Jim D.; Cioni, Raffaello; D'Antonio, Massimo

2016-04-01

One of the current stakes in modern volcanology is the definition of magma storage conditions which has direct implications on the eruptive style and thus on the associated risks and the management of likely related crisis. In alkaline differentiated magmas, chlorine (Cl), contrary to H2O, occurs as a minor volatile species but may be used as a geobarometer. Numerous experimental studies on Cl solubility have highlighted its saturation conditions in silicate melts. The NaCl-H2O system is characterized by immiscibility under wide ranges of pressure, temperature and NaCl content (pre-eruptive conditions, of utmost importance for the interpretation of the monitoring data and the identification of precursory signals.

Eruption and Degassing Processes in a Supervolcanic System: The Volatile Record Preserved in Melt Inclusions from the 3.49Ma Tara Ignimbrite in the Central Andes

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Grocke, S.; de Silva, S. L.; Schmitt, A. K.; Wallace, P. J.

2010-12-01

Analysis of H2O and CO2 in quartz and sanidine-hosted melt inclusions from one of the youngest supervolcanic eruptions in the Altiplano Puna Volcanic Complex (APVC) in the Central Andes provides information on crystallization depths and eruption and degassing processes. At least 740 km3 of high-K, metaluminous, rhyodacite to rhyolite magma erupted from the Guacha Caldera in southwest Bolivia, producing three phases of the 3.49 Ma Tara Ignimbrite: a Plinian fall-deposit, an extensive ignimbrite, and several post-caldera domes. Infrared spectroscopic analyses of quartz-hosted melt inclusions from Tara Plinian pumice have H2O contents of ~4.5 wt % and variable CO2 contents (110-300 ppm), corresponding to vapor saturation pressures up to 180 MPa. In contrast, sanidine-hosted melt inclusions from the Plinian-fall deposit contain bubbles, lower water contents (1.4-2.2 wt %) and lower CO2 (87-143 ppm). These vesiculated melt inclusions and low volatile contents suggest that the sanidine crystals leaked on their ascent to the surface and therefore do not record accurate pre-eruptive melt volatile contents. In contrast, quartz-hosted melt inclusions from post-caldera dome samples contain lower H2O contents of 2.5-3.5 wt % (average 2.9 wt %) and no detectable CO2, corresponding to vapor saturation pressures of 50-90 MPa. These data indicate that the preeruptive plinian stage Tara magma was vapor saturated at the time of melt inclusion entrapment and stored between 5-6 km, while those from the post-caldera domes were trapped at 2-3 km. Differences in CO2 between Plinian and dome melt inclusions require that the post-caldera dome quartzes represent a different generation of crystals that grew as the magma slowly rose and progressively degassed at 2-3 km. During this shallow crystallization, the magma evolved further and eventually fed the post-caldera domes, one of which is a high-Si rhyolite. Consistent with this interpretation, melt inclusions from post-caldera dome samples

Redox systematics of a magma ocean with variable pressure-temperature gradients and composition.

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Righter, K; Ghiorso, M S

2012-07-24

Oxygen fugacity in metal-bearing systems controls some fundamental aspects of the geochemistry of the early Earth, such as the FeO and siderophile trace element content of the mantle, volatile species that influence atmospheric composition, and conditions for organic compounds synthesis. Redox and metal-silicate equilibria in the early Earth are sensitive to oxygen fugacity (fO(2)), yet are poorly constrained in modeling and experimentation. High pressure and temperature experimentation and modeling in metal-silicate systems usually employs an approximation approach for estimating fO(2) that is based on the ratio of Fe and FeO [called "ΔIW (ratio)" hereafter]. We present a new approach that utilizes free energy and activity modeling of the equilibrium: Fe + SiO(2) + O(2) = Fe(2)SiO(4) to calculate absolute fO(2) and relative to the iron-wüstite (IW) buffer at pressure and temperature [ΔIW (P,T)]. This equilibrium is considered across a wide range of pressures and temperatures, including up to the liquidus temperature of peridotite (4,000 K at 50 GPa). Application of ΔIW (ratio) to metal-silicate experiments can be three or four orders of magnitude different from ΔIW (P,T) values calculated using free energy and activity modeling. We will also use this approach to consider the variation in oxygen fugacity in a magma ocean scenario for various thermal structures for the early Earth: hot liquidus gradient, 100 °C below the liquidus, hot and cool adiabatic gradients, and a cool subsolidus adiabat. The results are used to assess the effect of increasing P and T, changing silicate composition during accretion, and related to current models for accretion and core formation in the Earth. The fO(2) in a deep magma ocean scenario may become lower relative to the IW buffer at hotter and deeper conditions, which could include metal entrainment scenarios. Therefore, fO(2) may evolve from high to low fO(2) during Earth (and other differentiated bodies) accretion. Any

In-situ, high pressure and temperature experimental determination of hydrogen isotope fractionation between coexisting hydrous melt and silicate-saturated aqueous fluid

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Mysen, B. O.

2012-12-01

Hydrogen isotope fractionation between water-saturated silicate melt and silicate-saturated aqueous fluid has been determined experimentally, in-situ with the samples in the 450-800C and 101-1567 MPa temperature and pressure range, respectively. The temperatures are, therefore higher than those where hydrogen bonding in fluids and melts is important [1]. The experiments were conducted with a hydrothermal diamond anvil cell (HDAC) as the high-temperature/-pressure tool and vibrational spectroscopy to determine D/H fractionation. Compositions were along the haploandesite join, Na2Si4O9 - Na2(NaAl)4O9 [Al/(Al+Si)=0-0.1], and a 50:50 (by volume) H2O:D2O fluid mixture as starting material. Platinum metal was used to enhance equilibration rate. Isotopic equilibrium was ascertained by using variable experimental duration at given temperature and pressure. In the Al-free Na-silicate system, the enthalpy change of the (D/H) equilibrium of fluid is 3.1±0.7 kJ/mol, whereas for coexisting melt, ΔH=0 kJ/mol within error. With Al/(Al+Si)=0.1, ΔH=5.2±0.9 kJ/mol for fluid and near 0 within error for coexisting melt melt. For the exchange equilibrium between melt and fluid, H2O(melt)+D2O(fluid)=H2O(fluid)+D2O(melt), the ΔH=4.6±0.7 and 6.5±0.7 kJ/mol for the two Al-free and Al-bearing compositions, respectively, respectively. The D/H equilibration within fluids and melts and, therefore, D/H partitioning between coexisting fluid and melt reflect the influence of dissolved H2O(D2O) in melts and dissolved silicate components in H2O(D2O) fluid on their structure. The positive temperature- and pressure-dependence of silicate solubility and on silicate structure in silicate-saturated aqueous fluid governs the D/H fractionation in the fluid because increasing silicate solute concentration in fluid results in silicate polymerization [2]. These structural effects may be analogous to observed solute-dependent oxygen isotope fractionation between brine and CO2 [3]. In the temperature

Shallow Chamber & Conduit Behavior of Silicic Magma: A Thermo- and Fluid- Dynamic Parameterization Model of Physical Deformation as Constrained by Geodetic Observations: Case Study; Soufriere Hills Volcano, Montserrat

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Gunn de Rosas, C. L.

2013-12-01

The Soufrière Hills Volcano, Montserrat (SHV) is an active, mainly andesitic and well-studied stratovolcano situated at the northern end of the Lesser Antilles Arc subduction zone in the Caribbean Sea. The goal of our research is to create a high resolution 3D subsurface model of the shallow and deeper aspects of the magma storage and plumbing system at SHV. Our model will integrate inversions using continuous and campaign geodetic observations at SHV from 1995 to the present as well as local seismic records taken at various unrest intervals to construct a best-fit geometry, pressure point source and inflation rate and magnitude. We will also incorporate a heterogeneous media in the crust and use the most contemporary understanding of deep crustal- or even mantle-depth 'hot-zone' genesis and chemical evolution of silicic and intermediate magmas to inform the character of the deep edifice influx. Our heat transfer model will be constructed with a modified 'thin shell' enveloping the magma chamber to simulate the insulating or conducting influence of heat-altered chamber boundary conditions. The final forward model should elucidate observational data preceding and proceeding unrest events, the behavioral suite of magma transport in the subsurface environment and the feedback mechanisms that may contribute to eruption triggering. Preliminary hypotheses suggest wet, low-viscosity residual melts derived from 'hot zones' will ascend rapidly to shallower stall-points and that their products (eventually erupted lavas as well as stalled plutonic masses) will experience and display two discrete periods of shallow evolution; a rapid depressurization crystallization event followed by a slower conduction-controlled heat transfer and cooling crystallization. These events have particular implications for shallow magma behaviors, notably inflation, compressibility and pressure values. Visualization of the model with its inversion constraints will be affected with Com

Magma Transport from Deep to Shallow Crust and Eruption

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White, R. S.; Greenfield, T. S.; Green, R. G.; Brandsdottir, B.; Hudson, T.; Woods, J.; Donaldson, C.; Ágústsdóttir, T.

2016-12-01

We have mapped magma transport paths from the deep (20 km) to the shallow (6 km) crust and in two cases to eventual surface eruption under several Icelandic volcanoes (Askja, Bardarbunga, Eyjafjallajokull, Upptyppingar). We use microearthquakes caused by brittle fracture to map magma on the move and tomographic seismic studies of velocity perturbations beneath volcanoes to map the magma storage regions. High-frequency brittle failure earthquakes with magnitudes of typically 0-2 occur where melt is forcing its way through the country rock, or where previously frozen melt is repeatedly re-broken in conduits and dykes. The Icelandic crust on the rift zones where these earthquakes occur is ductile at depths greater than 7 km beneath the surface, so the occurrence of brittle failure seismicity at depths as great as 20 km is indicative of high strain rates, for which magma movement is the most likely explanation. We suggest that high volatile pressures caused by the exsolution of carbon dioxide in the deep crust is driving the magma movement and seismicity at depths of 15-20 km. Eruptions from shallow crustal storage areas are likewise driven by volatile exsolution, though additional volatiles, and in particular water are also involved in the shallow crust.

Temporal Evolution of Volcanic and Plutonic Magmas Related to Porphyry Copper Ores Based on Zircon Geochemistry

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Dilles, J. H.; Lee, R. G.; Wooden, J. L.; Koleszar, A. M.

2015-12-01

Porphyry Cu (Mo-Au) and epithermal Au-Ag ores are globally associated with shallow hydrous, strongly oxidized, and sulfur-rich arc intrusions. In many localities, long-lived magmatism includes evolution from early andesitic volcanic (v) and plutonic (p) rocks to later dacitic or rhyolitic compositions dominated by plutons. We compare zircon compositions from three igneous suites with different time spans: Yerington, USA (1 m.y., p>v), El Salvador, Chile (4 m.y., p>v), and Yanacocha, Peru (6 m.y., v>p). At Yerington granite dikes and ores formed in one event, at ES in 2 to 3 events spanning 3 m.y., and at Yanacocha in 6 events spanning 5 m.y. At both ES and Yanacocha, high-Al amphiboles likely crystallized at high temperature in the mid-crust and attest to deep magmas that periodically recharged the shallow chambers. At Yanacocha, these amphiboles contain anhydrite inclusions that require magmas were sulfur-rich and strongly oxidized (~NNO+2). The Ti-in-zircon geothermometer provides estimates of 920º to 620º C for zircon crystallization, and records both core to rim cooling and locally high temperature rim overgrowths. Ore-related silicic porphyries yield near-solidus crystallization temperatures of 750-650°C consistent with low zircon saturation temperatures. The latter zircons have large positive Ce/Ce* and small negative Eu/Eu*≥0.4 anomalies attesting to strongly oxidized conditions (Ballard et al., 2001), which we propose result from crystallization and SO2 loss to the magmatic-hydrothermal ore fluid (Dilles et al., 2015). The Hf, REE, Y, U, and Th contents of zircons are diverse in the magma suites, and Th/U vs Yb/Gd plots suggest a dominant role of crystal fractionation with lesser roles for both crustal contamination and mixing with high temperature deep-sourced mafic magma. Ce/Sm vs Yb/Gd plots suggest that magma REE contents at contamination are most evident in pre-ore magmas, whereas ore-forming intrusions at low temperatures are dominated by crystal

Evidence for a sulfur-undersaturated lunar interior from the solubility of sulfur in lunar melts and sulfide-silicate partitioning of siderophile elements

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Steenstra, E. S.; Seegers, A. X.; Eising, J.; Tomassen, B. G. J.; Webers, F. P. F.; Berndt, J.; Klemme, S.; Matveev, S.; van Westrenen, W.

2018-06-01

Sulfur concentrations at sulfide saturation (SCSS) were determined for a range of low- to high-Ti lunar melt compositions (synthetic equivalents of Apollo 14 black and yellow glass, Apollo 15 green glass, Apollo 17 orange glass and a late-stage lunar magma ocean melt, containing between 0.2 and 25 wt.% TiO2) as a function of pressure (1-2.5 GPa) and temperature (1683-1883 K). For the same experiments, sulfide-silicate partition coefficients were derived for elements V, Cr, Mn, Co, Cu, Zn, Ga, Ge, As, Se, Mo, Sn, Sb, Te, W and Pb. The SCSS is a strong function of silicate melt composition, most notably FeO content. An increase in temperature increases the SCSS and an increase in pressure decreases the SCSS, both in agreement with previous work on terrestrial, lunar and martian compositions. Previously reported SCSS values for high-FeO melts were combined with the experimental data reported here to obtain a new predictive equation to calculate the SCSS for high-FeO lunar melt compositions. Calculated SCSS values, combined with previously estimated S contents of lunar low-Ti basalts and primitive pyroclastic glasses, suggest their source regions were not sulfide saturated. Even when correcting for the currently inferred maximum extent of S degassing during or after eruption, sample S abundances are still > 700 ppm lower than the calculated SCSS values for these compositions. To achieve sulfide saturation in the source regions of low-Ti basalts and lunar pyroclastic glasses, the extent of degassing of S in lunar magma would have to be orders of magnitude higher than currently thought, inconsistent with S isotopic and core-to-rim S diffusion profile data. The only lunar samples that could have experienced sulfide saturation are some of the more evolved A17 high-Ti basalts, if sulfides are Ni- and/or Cu rich. Sulfide saturation in the source regions of lunar melts is also inconsistent with the sulfide-silicate partitioning systematics of Ni, Co and Cu. Segregation of

Magma reservoirs and neutral buoyancy zones on Venus - Implications for the formation and evolution of volcanic landforms

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Head, James W.; Wilson, Lionel

1992-01-01

The production of magma reservoirs and neutral buoyancy zones (NBZs) on Venus and the implications of their development for the formation and evolution of volcanic landforms are examined. The high atmospheric pressure on Venus reduces volatile exsolution and generally serves to inhibit the formation of NBZs and shallow magma reservoirs. For a range of common terrestrial magma-volatile contents, magma ascending and erupting near or below mean planetary radius (MPR) should not stall at shallow magma reservoirs; such eruptions are characterized by relatively high total volumes and effusion rates. For the same range of volatile contents at 2 km above MPR, about half of the cases result in the direct ascent of magma to the surface and half in the production of neutral buoyancy zones. NBZs and shallow magma reservoirs begin to appear as gas content increases and are nominally shallower on Venus than on earth. For a fixed volatile content, NBZs become deeper with increasing elevation: over the range of elevations treated in this study (-1 km to +4.4 km) depths differ by a factor of 2-4. Factors that may account for the low height of volcanoes on Venus are discussed.

Chondritic Mn/Na ratio and limited post-nebular volatile loss of the Earth

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Siebert, Julien; Sossi, Paolo A.; Blanchard, Ingrid; Mahan, Brandon; Badro, James; Moynier, Frédéric

2018-03-01

The depletion pattern of volatile elements on Earth and other differentiated terrestrial bodies provides a unique insight as to the nature and origin of planetary building blocks. The processes responsible for the depletion of volatile elements range from the early incomplete condensation in the solar nebula to the late de-volatilization induced by heating and impacting during planetary accretion after the dispersion of the H2-rich nebular gas. Furthermore, as many volatile elements are also siderophile (metal-loving), it is often difficult to deconvolve the effect of volatility from core formation. With the notable exception of the Earth, all the differentiated terrestrial bodies for which we have samples have non-chondritic Mn/Na ratios, taken as a signature of post-nebular volatilization. The bulk silicate Earth (BSE) is unique in that its Mn/Na ratio is chondritic, which points to a nebular origin for the depletion; unless the Mn/Na in the BSE is not that of the bulk Earth (BE), and has been affected by core formation through the partitioning of Mn in Earth's core. Here we quantify the metal-silicate partitioning behavior of Mn at deep magma ocean pressure and temperature conditions directly applicable to core formation. The experiments show that Mn becomes more siderophile with increasing pressure and temperature. Modeling the partitioning of Mn during core formation by combining our results with previous data at lower P-T conditions, we show that the core likely contains a significant fraction (20 to 35%) of Earth's Mn budget. However, we show that the derived Mn/Na value of the bulk Earth still lies on the volatile-depleted end of a trend defined by chondritic meteorites in a Mn/Na vs Mn/Mg plot, which tend to higher Mn/Na with increasing volatile depletion. This suggests that the material that formed the Earth recorded similar chemical fractionation processes for moderately volatile elements as chondrites in the solar nebula, and experienced limited post

Reconciling Gases With Glasses: Magma Degassing, Overturn and Mixing at Kilauea Volcano, Hawai`i

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Edmonds, M.; Gerlach, T. M.

2006-12-01

Our understanding of the volatile budget at Kilauea Volcano is based on measurements of the abundance of volatile elements in volcanic glasses and gases. Observations of volcanic gases gave rise to a fundamental model describing volatile fractionation between the summit and rift zone during the current eruption [Gerlach and Graeber, 1985]. Other workers' analysis of glasses from the Puna Ridge, Kilauea Iki and Pu`u `O`o indicate that magma degassing, drain-back, mixing and assimilation are important processes at Kilauea Volcano. Volcanic gases have not illustrated these kinds of processes clearly in the past, owing to infrequent and poorly resolved data. New, detailed studies of volcanic gas emissions have refined our understanding of volatile degassing and magma budgets at Kilauea Volcano. Open Path Fourier Transform Infra-Red spectroscopy measurements carried out during 2004-2005 allow retrieval of the relative abundances of the major volatile species H2O, CO2 and SO2, which together make up >99 vol% of the magmatic vapor phase. The proportions of these gases vary over time and space and can be used to infer magma transport, ascent, degassing, overturn and mixing and gas segregation processes within the plumbing system of Kilauea Volcano. Gases from Pu`u `O`o in 2004-2005 display a range in composition. A trend relates molar C/S to the total H2O content of the gases over time and space; total H2O ranges from 60-98 mol %, while molar C/S ranges from 50. The range in volcanic gas composition over time and space is caused by magma degassing, overturn and mixing of partially degassed magma with fresh primary magma beneath Pu`u `O`o. Measurements of the mean rate of magma degassing (from SO2 emissions) and mean lava effusion rate (from geophysical measurements of lava tube flux) suggest that a larger volume (DRE) of magma is degassing than is being erupted, on average. This analysis suggests that magma storage in the Rift Zone might be important during eruptions as

Numerical modeling perspectives on zircon crystallization and magma reservoir growth at the Laguna del Maule volcanic field, central Chile

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Andersen, N. L.; Dufek, J.; Singer, B. S.

2017-12-01

Magma reservoirs in the middle to upper crust are though to accumulate incrementally over 104 -105 years. Coupled crystallization ages and compositions of zircon are a potentially powerful tracer of reservoir growth and magma evolution. However, complex age distributions and disequilibrium trace element partitioning complicate the interpretation of the zircon record in terms of magmatic processes. In order to make quantitative predictions of the effects of magmatic processes that contribute reservoir growth and evolution—such as cooling and crystallization, magma recharge and mixing, and rejuvenation and remelting of cumulate-rich reservoir margins—we develop a model of zircon saturation and growth within a numerical framework of coupled thermal transfer, phase equilibrium, and magma dynamics. We apply this model to the Laguna del Maule volcanic field (LdM), located in central Chile. LdM has erupted at least 40 km3 of rhyolite from 36 vents distributed within a 250 km2 lake basin. Ongoing unrest demonstrates the large, silicic magma system beneath LdM remains active to this day. Zircon from rhyolite erupted between c. 23 and 1.8 ka produce a continuous distribution of 230Th-238U ages ranging from eruption to 40 ka, as well as less common crystal domains up to 165 ka and rare xenocrysts. Zircon trace element compositions fingerprint compositionally distinct reservoirs that grew within the larger magma system. Despite the dominantly continuous distributions of ages, many crystals are characterized by volumetrically substantial, trace element enriched domains consistent with rapid crystal growth. We utilize numerical simulations to assess the magmatic conditions required to catalyze these "blooms" of crystallization and the magma dynamics that contributed to the assembly of the LdM magma system.

A temporal record of pre-eruptive magmatic volatile contents at Campi Flegrei: Insights from texturally-constrained apatite analyses

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Stock, Michael J.; Isaia, Roberto; Humphreys, Madeleine C. S.; Smith, Victoria C.; Pyle, David M.

2016-04-01

Apatite is capable of incorporating all major magmatic volatile species (H2O, CO2, S, Cl and F) into its crystal structure. Analysis of apatite volatile contents can be related to parental magma compositions through the application of pressure and temperature-dependent exchange reactions (Piccoli and Candela, 1994). Once included within phenocrysts, apatite inclusions are isolated from the melt and preserve a temporal record of magmatic volatile contents in the build-up to eruption. In this work, we measured the volatile compositions of apatite inclusions, apatite microphenocrysts and pyroxene-hosted melt inclusions from the Astroni 1 eruption of Campi Flegrei, Italy (Stock et al. 2016). These data are coupled with magmatic differentiation models (Gualda et al., 2012), experimental volatile solubility data (Webster et al., 2014) and thermodynamic models of apatite compositional variations (Piccoli and Candela, 1994) to decipher pre-eruptive magmatic processes. We find that apatite halogen/OH ratios decreased through magmatic differentiation, while melt inclusion F and Cl concentrations increased. Melt inclusion H2O contents are constant at ~2.5 wt%. These data are best explained by volatile-undersaturated differentiation over most of the crystallisation history of the Astroni 1 melt, with melt inclusion H2O contents reset at shallow levels during ascent. Given the high diffusivity of volatiles in apatite (Brenan, 1993), the preservation of volatile-undersaturated melt compositions in microphenocrysts suggests that saturation was only achieved 10 - 103 days before eruption. We suggest that late-stage transition into a volatile-saturated state caused an increase in magma chamber overpressure, which ultimately triggered the Astroni 1 eruption. This has major implications for monitoring of Campi Flegrei and other similar volcanic systems. Piccoli and Candela, 1994. Am. J. of Sc., 294, 92-135. Stock et al., 2016, Nat. Geosci. Gualda et al., 2012. J. Pet., 53, 875

Redox Evolution in Magma Oceans Due to Ferric/Ferrous Iron Partitioning

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Schaefer, L.; Elkins-Tanton, L. T.; Pahlevan, K.

2017-12-01

A long-standing puzzle in the evolution of the Earth is that while the present day upper mantle has an oxygen fugacity close to the QFM buffer, core formation during accretion would have occurred at much lower oxygen fugacities close to IW. We present a new model based on experimental evidence that normal solidification and differentiation processes in the terrestrial magma ocean may explain both core formation and the current oxygen fugacity of the mantle without resorting to a change in source material or process. A commonly made assumption is that ferric iron (Fe3+) is negligible at such low oxygen fugacities [1]. However, recent work on Fe3+/Fe2+ ratios in molten silicates [2-4] suggests that the Fe3+ content should increase at high pressure for a given oxygen fugacity. While disproportionation was not observed in these experiments, it may nonetheless be occurring in the melt at high pressure [5]. Therefore, there may be non-negligible amounts of Fe3+ formed through metal-silicate equilibration at high pressures within the magma ocean. Homogenization of the mantle and further partitioning of Fe2+/Fe3+ as the magma ocean crystallizes may explain the oxygen fugacity of the Earth's mantle without requiring additional oxidation mechanisms. We present here models using different parameterizations for the Fe2+/Fe3+ thermodynamic relationships in silicate melts to constrain the evolution of the redox state of the magma ocean as it crystallizes. The model begins with metal-silicate partitioning at high pressure to form the core and set the initial Fe3+ abundance. Combined with previous work on oxygen absorption by magma oceans due to escape of H from H2O [6], we show that the upper layers of solidifying magma oceans should be more oxidized than the lower mantle. This model also suggests that large terrestrial planets should have more oxidized mantles than small planets. From a redox perspective, no change in the composition of the Earth's accreting material needs to be

Radiographic visualization of magma dynamics in an erupting volcano.

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Tanaka, Hiroyuki K M; Kusagaya, Taro; Shinohara, Hiroshi

2014-03-10

Radiographic imaging of magma dynamics in a volcanic conduit provides detailed information about ascent and descent of magma, the magma flow rate, the conduit diameter and inflation and deflation of magma due to volatile expansion and release. Here we report the first radiographic observation of the ascent and descent of magma along a conduit utilizing atmospheric (cosmic ray) muons (muography) with dynamic radiographic imaging. Time sequential radiographic images show that the top of the magma column ascends right beneath the crater floor through which the eruption column was observed. In addition to the visualization of this magma inflation, we report a sequence of images that show magma descending. We further propose that the monitoring of temporal variations in the gas volume fraction of magma as well as its position in a conduit can be used to support existing eruption prediction procedures.

Contribution of early impact events to metal-silicate separation, thermal annealing, and volatile redistribution: Evidence in the Pułtusk H chondrite

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Krzesińska, Agata M.

2017-11-01

Three-dimensional X-ray tomographic reconstructions and petrologic studies reveal voluminous accumulations of metal in Pułtusk H chondrite. At the contact of these accumulations, the chondritic rock is enriched in troilite. The rock contains plagioclase-rich bands, with textures suggesting crystallization from melt. Unusually large phosphates are associated with the plagioclase and consist of assemblages of merrillite, and fluorapatite and chlorapatite. The metal accumulations were formed by impact melting, rapid segregation of metal-sulfide melt and the incorporation of this melt into the fractured crater basement. The impact most likely occurred in the early evolution of the H chondrite parent body, when post-impact heat overlapped with radiogenic heat. This enabled slow cooling and separation of the metallic melt into metal-rich and sulfide-rich fractions. This led to recrystallization of chondritic rock in contact with the metal accumulations and the crystallization of shock melts. Phosphorus was liberated from the metal and subsumed by the silicate shock melt, owing to oxidative conditions upon slow cooling. The melt was also a host for volatiles. Upon further cooling, phosphorus reacted with silicates leading to the formation of merrillite, while volatiles partitioned into the residual halogen-rich, dry fluid. In the late stages, the fluid altered merrillite to patchy Cl/F-apatite. The above sequence of alterations demonstrates that impact during the early evolution of chondritic parent bodies might have contributed to local metal segregation and silicate melting. In addition, postshock conditions supported secondary processes: compositional/textural equilibration, redistribution of volatiles, and fluid alterations.

Long term storage of explosively erupted magma at Nevado de Toluca volcano, Mexico

Science.gov (United States)

Arce, J. L.; Gardner, J.; Macias, J. L.

2007-12-01

Dacitic magmas production is common in subduction-related volcanoes, occurring in those with a long period of activity as a result of the magmatic evolution. However, in this evolution many factors (i.e. crystal fractionation, assimilation, magma mixing) can interact to produce dacites. Nevado de Toluca volcano (4,680 masl; 19°09'N; 99°45'W) Central Mexico has recorded a long period of time producing dacites explosively, at least during 42 ka of activity, involving several km3 of magma, with two important Plinian-type eruptions occurred at ~21.7 ka (Lower Toluca Pumice) and ~10.5 ka (Upper Toluca Pumice). Questions like, what was the mechanism responsible to produce voluminous dacitic magma and how the volatiles and pressure changed in the Nevado de Toluca system, remain without answers. Dacites from the Lower Toluca Pumice (LTP) contain plagioclase, amphibole, iron-titanium oxides, and minor resorbed biotite, set in a glassy-vesicular matrix and the Upper Toluca Pumice (UTP) dacites contain the same mineral phases plus orthopyroxene. Ilmenite- ulvospinel geothermometry yielded a temperature of ~860°C for the LTP dacite, a little hotter than the UTP (~ 840°C). Based on hydrothermal experiments data, amphibole is stable above 100 MPa under 900°C, while plagioclase crystallizes up to 250-100 MPa at temperatures of 850-900°C. Pyroxene occurs only at pressures of 200-100 MPa with its respective temperatures of 825-900°C. Water contents in the LTP magma (2-3.5 wt %) are similar to that calculated for the UTP magma (1.3-3.6 wt %). So, there are only small changes in temperature and pressure from ~21.7 ka to 10.5 ka. It is noteworthy that orthopyroxene is absent in the LTP, however reaction-rimmed biotite (probably xenocrystic) is commonly observed in all dacites. Hence, almost all dacitic magmas seem to be stored at relatively similar pressures, water contents, and temperatures. All of these data could suggest repetitive basic magma injections producing the

The origin of volatiles in the Earth's mantle

Science.gov (United States)

Hier-Majumder, Saswata; Hirschmann, Marc M.

2017-08-01

The Earth's deep interior contains significant reservoirs of volatiles such as H, C, and N. Due to the incompatible nature of these volatile species, it has been difficult to reconcile their storage in the residual mantle immediately following crystallization of the terrestrial magma ocean (MO). As the magma ocean freezes, it is commonly assumed that very small amounts of melt are retained in the residual mantle, limiting the trapped volatile concentration in the primordial mantle. In this article, we show that inefficient melt drainage out of the freezing front can retain large amounts of volatiles hosted in the trapped melt in the residual mantle while creating a thick early atmosphere. Using a two-phase flow model, we demonstrate that compaction within the moving freezing front is inefficient over time scales characteristic of magma ocean solidification. We employ a scaling relation between the trapped melt fraction, the rate of compaction, and the rate of freezing in our magma ocean evolution model. For cosmochemically plausible fractions of volatiles delivered during the later stages of accretion, our calculations suggest that up to 77% of total H2O and 12% of CO2 could have been trapped in the mantle during magma ocean crystallization. The assumption of a constant trapped melt fraction underestimates the mass of volatiles in the residual mantle by more than an order of magnitude.Plain Language SummaryThe Earth's deep interior contains substantial amounts of volatile elements like C, H, and N. How these elements got sequestered in the Earth's interior has long been a topic of debate. It is generally assumed that most of these elements escaped the interior of the Earth during the first few hundred thousand years to create a primitive atmosphere, leaving the mantle reservoir nearly empty. In this work, we show that the key to this paradox involves the very early stages of crystallization of the mantle from a global magma ocean. Using numerical models, we show

The timing of compositionally-zoned magma reservoirs and mafic 'priming' weeks before the 1912 Novarupta-Katmai rhyolite eruption

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Singer, Brad S.; Costa, Fidel; Herrin, Jason S.; Hildreth, Wes; Fierstein, Judith

2016-01-01

The June 6, 1912 eruption of more than 13 km3 of dense rock equivalent (DRE) magma at Novarupta vent, Alaska was the largest of the 20th century. It ejected >7 km3 of rhyolite, ~1.3 km3 of andesite and ~4.6 km3 of dacite. Early ideas about the origin of pyroclastic flows and magmatic differentiation (e.g., compositional zonation of reservoirs) were shaped by this eruption. Despite being well studied, the timing of events that led to the chemically and mineralogically zoned magma reservoir remain poorly known. Here we provide new insights using the textures and chemical compositions of plagioclase and orthopyroxene crystals and by reevaluating previous U-Th isotope data. Compositional zoning of the magma reservoir likely developed a few thousand years before the eruption by several additions of mafic magma below an extant silicic reservoir. Melt compositions calculated from Sr contents in plagioclase fill the compositional gap between 68 and 76% SiO2 in whole pumice clasts, consistent with uninterrupted crystal growth from a continuum of liquids. Thus, our findings support a general model in which large volumes of crystal-poor rhyolite are related to intermediate magmas through gradual separation of melt from crystal-rich mush. The rhyolite is incubated by, but not mixed with, episodic recharge pulses of mafic magma that interact thermochemically with the mush and intermediate magmas. Hot, Mg-, Ca-, and Al-rich mafic magma intruded into, and mixed with, deeper parts of the reservoir (andesite and dacite) multiple times. Modeling the relaxation of the Fe-Mg concentrations in orthopyroxene and Mg in plagioclase rims indicates that the final recharge event occurred just weeks prior to the eruption. Rapid addition of mass, volatiles, and heat from the recharge magma, perhaps aided by partial melting of cumulate mush below the andesite and dacite, pressurized the reservoir and likely propelled a ~10 km lateral dike that allowed the overlying rhyolite to reach the surface.

Evidence of denser MgSiO3 glass above 133 gigapascal (GPa) and implications for remnants of ultradense silicate melt from a deep magma ocean.

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Murakami, Motohiko; Bass, Jay D

2011-10-18

Ultralow velocity zones are the largest seismic anomalies in the mantle, with 10-30% seismic velocity reduction observed in thin layers less than 20-40 km thick, just above the Earth's core-mantle boundary (CMB). The presence of silicate melts, possibly a remnant of a deep magma ocean in the early Earth, have been proposed to explain ultralow velocity zones. It is, however, still an open question as to whether such silicate melts are gravitationally stable at the pressure conditions above the CMB. Fe enrichment is usually invoked to explain why melts would remain at the CMB, but this has not been substantiated experimentally. Here we report in situ high-pressure acoustic velocity measurements that suggest a new transformation to a denser structure of MgSiO(3) glass at pressures close to those of the CMB. The result suggests that MgSiO(3) melt is likely to become denser than crystalline MgSiO(3) above the CMB. The presence of negatively buoyant and gravitationally stable silicate melts at the bottom of the mantle, would provide a mechanism for observed ultralow seismic velocities above the CMB without enrichment of Fe in the melt. An ultradense melt phase and its geochemical inventory would be isolated from overlying convective flow over geologic time.

Temperatures and isotopic evolution of silicic magmas, Taupo Volcanic Zone and Coromandel, New Zealand

International Nuclear Information System (INIS)

Blattner, P.; Rui-Zhong, Hu; Graham, I.J.; Houston-Eleftheriadis, C.

1996-01-01

A new set of oxygen and strontium isotope data on rhyolitic lavas and ignimbrites of the Taupo Volcanic Zone (TVZ) and the Coromandel Peninsula provides new limits for petrogenetic models. For oxygen isotopes, the rock matrix is frequently altered, so that values for magma need to be phenocryst based. Within TVZ a trend towards more negative delta 1 8 O values for more recent magmas appears likely (average before about 1 Ma and for Coromandel near 8.0 per thousand; after 1 Ma near 7.5 per thousand). This could indicate the gradual removal of supracrustal contaminants from the zones of magma accumulation and extrusion. Similar trends within Coromandel cannot yet be resolved. A generally positive correlation is found for oxygen and strontium isotopes of magmas. Most magmas have a limited range of isotopic values, which then becomes a useful fingerprint (e.g., the Mamaku, Matahina, and Waiotapu Ignimbrites). A narrow range of eruption temperatures of 880 plus or minus 60degC is derived from quartz-plagioclase fractionations of 0.98 plus or minus 0.25 per thousand delta 1 8 O for 15 magmas. Some delta 1 8 O values of quartz and feldspar phenocrysts are sufficiently low to suggest interaction between surface water and magma. However, large negative oxygen isotope anomalies (such as known from Yellowstone), could be no more than partially concealed by the isotopically less depleted meteoric water of New Zealand, and have not yet been found in New Zealand. (author). 45 refs., 3 tabs., 6 figs

Interior Volatile Reservoirs in Mercury

Science.gov (United States)

Anzures, B. A.; Parman, S. W.; Milliken, R. E.; Head, J. W.

2018-05-01

More measurements of 1) surface volatiles, and 2) pyroclastic deposits paired with experimental volatile analyses in silicate minerals can constrain conditions of melting and subsequent eruption on Mercury.

Chlorine as a geobarometer tool: Application to the large explosive eruptions of Vesuvius

Science.gov (United States)

Balcone-Boissard, Hélène; Boudon, Georges; Cioni, Raffaello; Zdanowicz, Géraldine; Orsi, Giovanni; Civetta, Lucia

2015-04-01

One of the current stakes in modern volcanology is the definition of magma storage conditions which has direct implications on the eruptive style and thus on the associated risks and the management of likely related crisis. In alkaline differentiated magmas, chlorine (Cl), contrary to H2O, occurs as a minor volatile species but may be used as a geobarometer. Numerous experimental studies on Cl solubility have highlighted its saturation conditions in alkaline silicate melts. The NaCl-H2O system is characterized by immiscibility under wide ranges of pressure, temperature and NaCl content (pre-eruptive H2O content for the different magma compositions, varying between 3.5 and 7 wt%. The results, in large agreement with literature, are very promising. The Cl geobarometer may help scientists to define the reservoir dynamics through time and provide strong constraints on pre-eruptive conditions, of outmost importance for the interpretation of the monitoring data and the identification of precursory signals.

In defense of Magnetite-Ilmenite Thermometry in the Bishop Tuff and its implication for gradients in silicic magma reservoirs

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Evans, Bernard W; Hildreth, Edward; Bachmann, Olivier; Scaillet, Bruno

2016-01-01

Despite claims to the contrary, the compositions of magnetite and ilmenite in the Bishop Tuff correctly record the changing conditions of T and fO2 in the magma reservoir. In relatively reduced (∆NNO magmas (e.g., Bishop Tuff, Taupo units), Ti behaves compatibly (DTi ≈ 2-3.5), leading to a decrease in TiO2 activity in the melt with cooling and fractionation. In contrast, FeTi-oxides are poorer in TiO2 in more oxidized magmas (∆NNO > 1, e.g., Fish Canyon Tuff, Pinatubo), and the d(aTiO2)/dT slope can be negative. Biotite, FeTi-oxides, liquid, and possibly plagioclase largely maintained equilibrium in the Bishop Tuff magma (unlike the pyroxenes, and cores of quartz, sanidine, and zircon) prior ro and during a mixing event triggered by a deeper recharge, which, based on elemental diffusion profiles in minerals, took place at least several decades before eruption. Equilibrating phases and pumice compositions show evolving chemical variations that correlate well with mutually consistent temperatures based on the FeTi-oxides, sanidine-plagioclase, and ∆18O quartz-magnetite pairs. Early Bishop Tuff (EBT) temperatures are lower (700 to ~780‎°C) than temperatures (780 to >820°C) registered in Late Bishop Tuff (LBT), the latter defined here not strictly stratigraphically, but by the presence of orthopyroxene and reverse-zoned rims on quartz and sanidine. The claimed similarity in compositions, Zr-saturation temperatures and thermodynamically calculated temperatures (730-740°C) between EBT and less evolved LBT reflect the use of glass inclusions in quartz cores in LBT that were inherited from the low temperature rhyolitic part of the reservoir characteristic of the EBT. LBT temperatures as high as 820°C, the preservation of orthopyroxene, and the presence of reverse-zoned minerals (quartz, sanidine, zircons) are consistent with magma recharge at the base of the zoned reservoir, heating the cooler rhyolitic melt, partly remelting cumulate mush, and introducing

Effects of Rotation on the Differentiation of a terrestrial Magma Ocean

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Maas, C.; Hansen, U.

2014-12-01

It is widely accepted that the Earth experienced several large impacts during its early evolution which led to the formation of one or more magma oceans. Differentiation processes in such a magma ocean are of great importance for the initial conditions of mantle convection and for the subsequent mantle structure. Convection in a magma ocean is most likely very vigorous. Further, rotation of the early Earth is supposed to be very fast. Therefore, and due to the small viscosity, it can be assumed that differentiation is strongly affected by rotation.To study the influence of rotation on the crystallization of a magma ocean, we employed a 3D Cartesian numerical model with low Prandtl number and used a discrete element method to describe silicate crystals.Our results show a crucial dependence on crystal density, rotation rate and latitude. Low rotation at the pole leads to a large fraction of suspended particles. With increasing rotation the particles settle at the bottom and form a stable stratified layer. In contrast to that at the equator at low rotation all particles settle at the bottom, at higher rotation they form a layer of significant thickness and at the highest rotation rate the particles accumulate in the middle of the magma ocean. In addition to that, we observe that due to the Coriolis force silicate crystals with different densities separate from each other. While lighter particles are at the bottom, denser particles accumulate at mid-depth at the same rotation rate. This could result in an unstable stratified mantle in the equatorial region after magma ocean solidification.All in all, rotation could lead to an asymmetrical crystallization of the magma ocean, with a contrary layering at the pole and the equator. This affects the composition of the early mantle and could explain the development of a localized magma ocean at the core-mantle boundary and the development of phase transitions observed in seismology, like the mantle transition zone.

Lunar magma transport phenomena

Science.gov (United States)

Spera, Frank J.

1992-01-01

An outline of magma transport theory relevant to the evolution of a possible Lunar Magma Ocean and the origin and transport history of the later phase of mare basaltic volcanism is presented. A simple model is proposed to evaluate the extent of fractionation as magma traverses the cold lunar lithosphere. If Apollo green glasses are primitive and have not undergone significant fractionation en route to the surface, then mean ascent rates of 10 m/s and cracks of widths greater than 40 m are indicated. Lunar tephra and vesiculated basalts suggest that a volatile component plays a role in eruption dynamics. The predominant vapor species appear to be CO CO2, and COS. Near the lunar surface, the vapor fraction expands enormously and vapor internal energy is converted to mixture kinetic energy with the concomitant high-speed ejection of vapor and pyroclasts to form lunary fire fountain deposits such as the Apollo 17 orange and black glasses and Apollo 15 green glass.

Temperatures and isotopic evolution of silicic magmas, Taupo Volcanic Zone and Coromandel, New Zealand

International Nuclear Information System (INIS)

Blattner, P.; Rui-Zhong H.; Graham, I.J.; Houston-Eleftheriadis, C.

1996-01-01

A new set of oxygen and strontium isotope data on rhyolitic lavas and ignimbrites of the Taupo Volcanic Zone (TVZ) and the Coromandel Peninsula provides new limits for petrogenic models. For oxygen isotopes, the rock matrix is frequently altered, so that values for magma need to be phenocryst based. Within TVZ a trend towards more negative δ 1 8O values for more recent magmas appears likely (average before about 1 Ma and for Coromandel near 8.0 per mille; after 1 Ma near 7.5 per mille). This could indicate the gradual removal of supracrustal contaminants from the zones of magma accumulation and extrusion. Similar trends within Coromandel cannot yet be resolved. A generally positive correlation is found for oxygen and strontium isotopes of magmas. Most magmas have a limited range of isotopic values, which then becomes a fingerprint (e.g., the Mamaku, Matahina, and Waiotapu Ignimbrites). A narrow range of eruption temperatures of 880 ± 60 o C is derived from quartz-plagioclase fractionations of 0.98 ± 0.25 per mille δ 1 8O values of quartz and feldspar phenocrysts are sufficiently low to suggest interaction between surface water and magma. However, large negative oxygen isotope anomalies (such as known from Yellowstone), could be no more than partially concealed by the isotopically less depleted meteoric water of New Zealand, and have not yet been found in New Zealand. (authors). 45 refs., 6 figs., 3 tabs

Superheat in magma oceans

Science.gov (United States)

Jakes, Petr

1992-01-01

The existence of 'totally molten' planets implies the existence of a superheat (excess of heat) in the magma reservoirs since the heat buffer (i.e., presence of crystals having high latent heat of fusion) does not exist in a large, completely molten reservoir. Any addition of impacting material results in increase of the temperature of the melt and under favorable circumstances heat is stored. The behavior of superheat melts is little understood; therefore, we experimentally examined properties and behavior of excess heat melts at atmospheric pressures and inert gas atmosphere. Highly siliceous melts (70 percent SiO2) were chosen for the experiments because of the possibility of quenching such melts into glasses, the slow rate of reaction in highly siliceous composition, and the fact that such melts are present in terrestrial impact craters and impact-generated glasses. Results from the investigation are presented.

A Thermodynamic Approach for Modeling H2O-CO2 Solubility in Alkali-rich Mafic Magmas at Mid-crustal Pressures

Science.gov (United States)

Allison, C. M.; Roggensack, K.; Clarke, A. B.

2017-12-01

Volatile solubility in magmas is dependent on several factors, including composition and pressure. Mafic (basaltic) magmas with high concentrations of alkali elements (Na and K) are capable of dissolving larger quantities of H2O and CO2 than low-alkali basalt. The exsolution of abundant gases dissolved in alkali-rich mafic magmas can contribute to large explosive eruptions. Existing volatile solubility models for alkali-rich mafic magmas are well calibrated below 200 MPa, but at greater pressures the experimental data is sparse. To allow for accurate interpretation of mafic magmatic systems at higher pressures, we conducted a set of mixed H2O-CO2 volatile solubility experiments between 400 and 600 MPa at 1200 °C in six mafic compositions with variable alkali contents. Compositions include magmas from volcanoes in Italy, Antarctica, and Arizona. Results from our experiments indicate that existing volatile solubility models for alkali-rich mafic magmas, if extrapolated beyond their calibrated range, over-predict CO2 solubility at mid-crustal pressures. Physically, these results suggest that volatile exsolution can occur at deeper levels than what can be resolved from the lower-pressure experimental data. Existing thermodynamic models used to calculate volatile solubility at different pressures require two experimentally derived parameters. These parameters represent the partial molar volume of the condensed volatile species in the melt and its equilibrium constant, both calculated at a standard temperature and pressure. We derived these parameters for each studied composition and the corresponding thermodynamic model shows good agreement with the CO2 solubility data of the experiments. A general alkali basalt solubility model was also constructed by establishing a relationship between magma composition and the thermodynamic parameters. We utilize cation fractions from our six compositions along with four compositions from the experimental literature in a linear

Noble Gas Isotope Evidence for Mantle Volatiles in the Cu-Mo Porphyry and Main Stage Polymetallic Veins at Butte, Montana

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Hofstra, A. H.; Rusk, B. G.; Manning, A. H.; Hunt, A. G.; Landis, G. P.

2017-12-01

Recent studies suggest that volatiles released from mafic intrusions may be important sources of heat, sulfur, and metals in porphyry Cu-Mo-Au and epithermal Au-Ag deposits associated with intermediate to silicic stocks. The huge Cu-Mo porphyry and Main Stage polymetallic vein deposits at Butte are well suited to test this hypothesis because there is no geologic or isotopic evidence of basaltic intrusions in the mine or drill holes. The Butte porphyry-vein system is associated with quartz monzonite stocks and dikes within the southwest part of the Late Cretaceous Boulder batholith. The Boulder batholith was emplaced into Mesoproterozoic to Mesozoic sedimentary rocks and Late Cretaceous volcanic rocks. The Boulder batholith and Butte intrusions have Sri and eNd values indicative of crustal contamination. Eu and Ce anomalies in zircon from Butte intrusions provide evidence of oxidation due to magma degassing. To ascertain the source of volatiles in this system, 11 samples from the Cu-Mo porphyry and 16 from Main Stage veins were selected. The isotopic composition of Ar, Ne, and He extracted from fluid inclusions in quartz, magnetite, pyrite, chalcopyrite, sphalerite, galena, enargite, and covellite were determined. Helium isotopes exceed blank levels in all samples and Ne and Ar in some samples. On a 38Ar/36Ar vs. 40Ar/36Ar diagram, data plot near air. On a 20Ne/22Ne vs. 21Ne/22Ne diagram, data extend from air along the trajectories of OIB and MORB. On a 36Ar/4He vs. 3He/4He RA diagram, data extend from crust toward the air-mantle mixing line. The maximum 3He/4He RA values in the Cu-Mo porphyry (2.86) and Main Stage veins (3.46) are from pyrite and these values correspond to 36 and 43 % mantle helium. The Ne and He results show that fluid inclusions contain volatiles discharged from mantle magmas and that these volatiles were diluted by groundwater containing He derived from country rocks. Despite the lack of mafic intrusions in the Butte magmatic center, noble gas

Evolution of C-O-H-N volatile species in the magma ocean during core formation.

Science.gov (United States)

Dalou, C.; Le Losq, C.; Hirschmann, M. M.; Jacobsen, S. D.; Fueri, E.

2017-12-01

The composition of the Hadean atmosphere affected how life began on Earth. Magma ocean degassing of C, O, H, and N was a key influence on the composition of the Hadean atmosphere. To identify the nature of degassed C-O-H-N species, we determined their speciation in reduced basaltic glasses (in equilibrium with Fe-C-N metal alloy, synthetized at 1400 and 1600 ºC and 1.2-3 GPa) via Raman spectroscopy. We addressed the effect of oxygen fugacity (fO2) on C-O-H-N speciation between IW-2.3 and IW-0.4, representing the evolution of the shallow upper mantle fO2 during the Hadean. We observe H2, NH2, NH3, CH3, CH4, CO, N2, and OH species in all glasses. With increasing ƒO2, our results support the formation of OH groups at the expense of N-H and C-H bonds in the melt, implying the equilibria at IW-2: (1) 2OH- (melt) + ½ N2 (melt) ↔ NH2 (melt) + 2 O2- (melt) , (2) 2OH- (melt) + ½ N2 (melt) + ½ H2 (melt) ↔ NH3 (melt) + 2 O2- (melt) . With increasing fO2, eqs. (1) and (2) shift to the left. From IW-2 to IW, we also observe an increase in the intensity of the NH2 peak relative to NH3. Carbon is present as CH3, CH4, and CO in all our glasses. While CO is likely the main carbon specie under reduced conditions (e.g., Armstrong et al. 2015), CH species should remain stable from moderately (IW-0.4) to very reduced (IW-3; Ardia et al. 2014; Kadik et al. 2015, 2017) conditions in hydrous silicate glasses following the equilibria: (3) 3OH- (melt) + C (graphite) ↔ CH3 (melt) + 3O2- (melt) , (4) 4OH- (melt) + C (graphite) ↔ CH4 (melt) + 4O2- (melt) . With increasing fO2, eqs. (3) and (4) shift to the left. As metal segregation and core formation drove the ƒO2 of the magma ocean from IW-4 to IW during the Hadean (Rubie et al. 2011), the nature of species degassed by the magma ocean should have evolved during that time. The C-O-H-N species we observe dissolved in our reduced glasses may not directly correspond to those degassed (Schaeffer and Fegley, 2007), but a better

Magma storage in a strike-slip caldera.

Science.gov (United States)

Saxby, J; Gottsmann, J; Cashman, K; Gutiérrez, E

2016-07-22

Silicic calderas form during explosive volcanic eruptions when magma withdrawal triggers collapse along bounding faults. The nature of specific interactions between magmatism and tectonism in caldera-forming systems is, however, unclear. Regional stress patterns may control the location and geometry of magma reservoirs, which in turn may control the spatial and temporal development of faults. Here we provide new insight into strike-slip volcano-tectonic relations by analysing Bouguer gravity data from Ilopango caldera, El Salvador, which has a long history of catastrophic explosive eruptions. The observed low gravity beneath the caldera is aligned along the principal horizontal stress orientations of the El Salvador Fault Zone. Data inversion shows that the causative low-density structure extends to ca. 6 km depth, which we interpret as a shallow plumbing system comprising a fractured hydrothermal reservoir overlying a magmatic reservoir with vol% exsolved vapour. Fault-controlled localization of magma constrains potential vent locations for future eruptions.

The chemical and isotopic differentiation of an epizonal magma body: Organ Needle pluton, New Mexico

Science.gov (United States)

Verplanck, P.L.; Farmer, G.L.; McCurry, M.; Mertzman, S.A.

1999-01-01

Major and trace element, and Nd and Sr isotopic compositions of whole rocks and mineral separates from the Oligocene, alkaline Organ Needle pluton (ONP), southern New Mexico, constrain models for the differentiation of the magma body parental to this compositionally zoned and layered epizonal intrusive body. The data reveal that the pluton is rimmed by lower ??(Nd) (~-5) and higher 87Sr/86Sr (~0.7085) syenitic rocks than those in its interior (??(Nd) ~ 2, 87Sr/86Sr ~0.7060) and that the bulk compositions of the marginal rocks become more felsic with decreasing structural depth. At the deepest exposed levels of the pluton, the ??(Nd)~-5 lithology is a compositionally heterogeneous inequigranular syenite. Modal, compositional and isotopic data from separates of rare earth element (REE)-bearing major and accesory mineral phases (hornblende, titanite, apatite, zircon) demonstrate that this decoupling of trace and major elements in the inequigranular syenite results from accumulation of light REE (LREE)-bearing minerals that were evidently separated from silicic magmas as the latter rose along the sides of the magma chamber. Chemical and isotopic data for microgranular mafic enclaves, as well as for restite xenoliths of Precambrian granite wall rock, indicate that the isotopic distinction between the marginal and interior facies of the ONP probably reflects assimilation of the wall rock by ??(Nd) ~-2 mafic magmas near the base of the magma system. Fractional crystallization and crystal liquid separation of the crystally contaminated magma at the base and along the margins of the chamber generated the highly silicic magmas that ultimately pooled at the chamber top.

Partitioning of U, Th and K Between Metal, Sulfide and Silicate, Insights into the Volatile-Content of Mercury

Science.gov (United States)

Habermann, M.; Boujibar, A.; Righter, K.; Danielson, L.; Rapp, J.; Righter, M.; Pando, K.; Ross, D. K.; Andreasen, R.; Chidester, B.

2016-01-01

During the early stages of the Solar System formation, especially during the T-Tauri phase, the Sun emitted strong solar winds, which are thought to have expelled a portion of the volatile elements from the inner solar system. It is therefore usually believed that the volatile depletion of a planet is correlated with its proximity to the Sun. This trend was supported by the K/Th and K/U ratios of Venus, the Earth, and Mars. Prior to the MESSENGER mission, it was expected that Mercury is the most volatile-depleted planet. However, the Gamma Ray Spectrometer of MESSENGER spacecraft revealed elevated K/U and K/Th ratios for the surface of Mercury, much higher than previous expectations. It is possible that the K/Th and K/U ratios on the surface are not a reliable gauge of the bulk volatile content of Mercury. Mercury is enriched in sulfur and is the most reduced of the terrestrial planets, with oxygen fugacity (fO2) between IW-6.3 and IW-2.6 log units. At these particular compositions, U, Th and K behave differently and can become more siderophile or chalcophile. If significant amounts of U and Th are sequestered in the core, the apparent K/U and K/Th ratios measured on the surface may not represent the volatile budget of the whole planet. An accurate determination of the partitioning of these elements between silicate, metal, and sulfide phases under Mercurian conditions is therefore essential to better constrain Mercury's volatile content and assess planetary formation models.

Magma heating by decompression-driven crystallization beneath andesite volcanoes.

Science.gov (United States)

Blundy, Jon; Cashman, Kathy; Humphreys, Madeleine

2006-09-07

Explosive volcanic eruptions are driven by exsolution of H2O-rich vapour from silicic magma. Eruption dynamics involve a complex interplay between nucleation and growth of vapour bubbles and crystallization, generating highly nonlinear variation in the physical properties of magma as it ascends beneath a volcano. This makes explosive volcanism difficult to model and, ultimately, to predict. A key unknown is the temperature variation in magma rising through the sub-volcanic system, as it loses gas and crystallizes en route. Thermodynamic modelling of magma that degasses, but does not crystallize, indicates that both cooling and heating are possible. Hitherto it has not been possible to evaluate such alternatives because of the difficulty of tracking temperature variations in moving magma several kilometres below the surface. Here we extend recent work on glassy melt inclusions trapped in plagioclase crystals to develop a method for tracking pressure-temperature-crystallinity paths in magma beneath two active andesite volcanoes. We use dissolved H2O in melt inclusions to constrain the pressure of H2O at the time an inclusion became sealed, incompatible trace element concentrations to calculate the corresponding magma crystallinity and plagioclase-melt geothermometry to determine the temperature. These data are allied to ilmenite-magnetite geothermometry to show that the temperature of ascending magma increases by up to 100 degrees C, owing to the release of latent heat of crystallization. This heating can account for several common textural features of andesitic magmas, which might otherwise be erroneously attributed to pre-eruptive magma mixing.

Rapid heterogeneous assembly of multiple magma reservoirs prior to Yellowstone supereruptions.

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Wotzlaw, Jörn-Frederik; Bindeman, Ilya N; Stern, Richard A; D'Abzac, Francois-Xavier; Schaltegger, Urs

2015-09-10

Large-volume caldera-forming eruptions of silicic magmas are an important feature of continental volcanism. The timescales and mechanisms of assembly of the magma reservoirs that feed such eruptions as well as the durations and physical conditions of upper-crustal storage remain highly debated topics in volcanology. Here we explore a comprehensive data set of isotopic (O, Hf) and chemical proxies in precisely U-Pb dated zircon crystals from all caldera-forming eruptions of Yellowstone supervolcano. Analysed zircons record rapid assembly of multiple magma reservoirs by repeated injections of isotopically heterogeneous magma batches and short pre-eruption storage times of 10(3) to 10(4) years. Decoupled oxygen-hafnium isotope systematics suggest a complex source for these magmas involving variable amounts of differentiated mantle-derived melt, Archean crust and hydrothermally altered shallow-crustal rocks. These data demonstrate that complex magma reservoirs with multiple sub-chambers are a common feature of rift- and hotspot related supervolcanoes. The short duration of reservoir assembly documents rapid crustal remelting and two to three orders of magnitude higher magma production rates beneath Yellowstone compared to continental arc volcanoes. The short pre-eruption storage times further suggest that the detection of voluminous reservoirs of eruptible magma beneath active supervolcanoes may only be possible prior to an impending eruption.

Tube pumices as strain markers of the ductile-brittle transition during magma fragmentation

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Martí, J.; Soriano, C.; Dingwell, D. B.

1999-12-01

Magma fragmentation-the process by which relatively slow-moving magma transforms into a violent gas flow carrying fragments of magma-is the defining feature of explosive volcanism. Yet of all the processes involved in explosively erupting systems, fragmentation is possibly the least understood. Several theoretical and laboratory studies on magma degassing and fragmentation have produced a general picture of the sequence of events leading to the fragmentation of silicic magma. But there remains a debate over whether magma fragmentation is a consequence of the textural evolution of magma to a foamed state where disintegration of walls separating bubbles becomes inevitable due to a foam-collapse criterion, or whether magma is fragmented purely by stresses that exceed its tensile strength. Here we show that tube pumice-where extreme bubble elongation is observed-is a well-preserved magmatic `strain marker' of the stress state immediately before and during fragmentation. Structural elements in the pumice record the evolution of the magma's mechanical response from viscous behaviour (foaming and foam elongation) through the plastic or viscoelastic stage, and finally to brittle behaviour. These observations directly support the hypothesis that fragmentation occurs when magma undergoes a ductile-brittle transition and stresses exceed the magma's tensile strength.

Core Formation on Asteroid 4 Vesta: Iron Rain in a Silicate Magma Ocean

Science.gov (United States)

Kiefer, Walter S.; Mittlefehldt, David W.

2017-01-01

Geochemical observations of the eucrite and diogenite meteorites, together with observations made by NASA's Dawn spacecraft, suggest that Vesta resembles H chondrites in bulk chemical composition, possibly with about 25% of a CM-chondrite like composition added in. For this model, the core is 15% by mass (or 8 volume %) of the asteroid. The abundances of moderately siderophile elements (Ni, Co, Mo, W, and P) in eucrites require that essentially all of the metallic phase in Vesta segregated to form a core prior to eucrite solidification. Melting in the Fe-Ni-S system begins at a cotectic temperature of 940 deg. C. Only about 40% of the total metal phase, or 3-4 volume % of Vesta, melts prior to the onset of silicate melting. Liquid iron in solid silicate initially forms isolated pockets of melt; connected melt channels, which are necessary if the metal is to segregate from the silicate, are only possible when the metal phase exceeds about 5 volume %. Thus, metal segregation to form a core does not occur prior to the onset of silicate melting.

The role of volatile-saturation and adiabatic ascent of moderately hydrous melts on the formation of orbicules and comb layers in shallow subvolcanic conduits (Fisher Lake, Sierra Nevada).

Science.gov (United States)

McCarthy, A. J.; Müntener, O.

2016-12-01

Orbicules and comb layers are enigmatic features found sparsely distributed along plutonic contacts in a wide range of igneous environments. We provide new insights into the mechanisms responsible for the formation of these features by studying the spatial distribution, mineralogy and geochemistry of comb layers and orbicules from the Northern Sierra Nevada, Fisher Lake (USA). Over a range of studied comb textured layering, we show that the large majority of comb layers are cumulates formed by the initiation of plagioclase growth as a comb textured mineral. Plagioclase fractionation is followed by pyroxenes + oxides fractionation. Continuous crystal fractionation and conductive cooling from the host rock leads to amphibole saturation and the formation of late stage comb textured amphibole, leading to the formation of plagioclase- and plagioclase-amphibole comb textures. The lack of amphibole comb textures on orbicule rims as opposed to their widespread occurrence in comb layers, suggests that the presence of a thermal gradient plays an important role in diversifying comb textures. We propose that comb layers and orbicules are unique features which are controlled by the volatile content of ascending melts and ascent mechanisms. Thermodynamic calculations indicate that near-adiabatic decompression of water-undersaturated melts (ca. 4wt% H2O) through the crust will lead to superheating and dissolution of pre-existing minerals. Upon saturation of volatiles at shallow depth, degassing-induced undercooling of the decompressing melt will trigger heterogeneous nucleation of plagioclase on host rocks and remobilized xenoliths. The rarity of orbicules and comb layers in volcanic and plutonic rocks worldwide suggests that adiabatic decompression of moderately hydrous melts leading to superheating is a rare phenomena, with most arc melts ascending and cooling in small reservoirs throughout the crust, prior to emplacement at shallow depth as crystal-bearing magmas.

Lead and strontium isotopic evidence for crustal interaction and compositional zonation in the source regions of Pleistocene basaltic and rhyolitic magmas of the Coso volcanic field, California

Science.gov (United States)

Bacon, C.R.; Kurasawa, H.; Delevaux, M.H.; Kistler, R.W.; Doe, B.R.

1984-01-01

The isotopic compositions of Pb and Sr in Pleistocene basalt, high-silica rhyolite, and andesitic inclusions in rhyolite of the Coso volcanic field indicate that these rocks were derived from different levels of compositionally zoned magmatic systems. The 2 earliest rhyolites probably were tapped from short-lived silicic reservoirs, in contrast to the other 36 rhyolite domes and lava flows which the isotopic data suggest may have been leaked from the top of a single, long-lived magmatic system. Most Coso basalts show isotopic, geochemical, and mineralogic evidence of interaction with crustal rocks, but one analyzed flow has isotopic ratios that may represent mantle values (87Sr/86Sr=0.7036,206Pb/204Pb=19.05,207Pb/204Pb=15.62,208Pb/204Pb= 38.63). The (initial) isotopic composition of typical rhyolite (87Sr/86Sr=0.7053,206Pb/204Pb=19.29,207Pb/204Pb= 15.68,208Pb/204Pb=39.00) is representative of the middle or upper crust. Andesitic inclusions in the rhyolites are evidently samples of hybrid magmas from the silicic/mafic interface in vertically zoned magma reservoirs. Silicic end-member compositions inferred for these mixed magmas, however, are not those of erupted rhyolite but reflect the zonation within the silicic part of the magma reservoir. The compositional contrast at the interface between mafic and silicic parts of these systems apparently was greater for the earlier, smaller reservoirs. ?? 1984 Springer-Verlag.

Seismic Tremors and Three-Dimensional Magma Wagging

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Liao, Y.; Bercovici, D.

2015-12-01

Seismic tremor is a feature shared by many silicic volcanoes and is a precursor of volcanic eruption. Many of the characteristics of tremors, including their frequency band from 0.5 Hz to 7 Hz, are common for volcanoes with very different geophysical and geochemical properties. The ubiquitous characteristics of tremor imply that it results from some generation mechanism that is common to all volcanoes, instead of being unique to each volcano. Here we present new analysis on the magma-wagging mechanism that has been proposed to generate tremor. The model is based on the suggestion given by previous work (Jellinek & Bercovici 2011; Bercovici et.al. 2013) that the magma column is surrounded by a compressible, bubble-rich foam annulus while rising inside the volcanic conduit, and that the lateral oscillation of the magma inside the annulus causes observable tremor. Unlike the previous two-dimensional wagging model where the displacement of the magma column is restricted to one vertical plane, the three-dimensional model we employ allows the magma column to bend in different directions and has angular motion as well. Our preliminary results show that, without damping from viscous deformation of the magma column, the system retains angular momentum and develops elliptical motion (i.e., the horizontal displacement traces an ellipse). In this ''inviscid'' limit, the magma column can also develop instabilities with higher frequencies than what is found in the original two-dimensional model. Lateral motion can also be out of phase for various depths in the magma column leading to a coiled wagging motion. For the viscous-magma model, we predict a similar damping rate for the uncoiled magma column as in the two-dimensional model, and faster damping for the coiled magma column. The higher damping thus requires the existence of a forcing mechanism to sustain the oscillation, for example the gas-driven Bernoulli effect proposed by Bercovici et al (2013). Finally, using our new 3

The role of liquid-liquid immiscibility and crystal fractionation in the genesis of carbonatite magmas: insights from Kerimasi melt inclusions

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Guzmics, Tibor; Zajacz, Zoltán; Mitchell, Roger H.; Szabó, Csaba; Wälle, Markus

2015-02-01

We have reconstructed the compositional evolution of the silicate and carbonate melt, and various crystalline phases in the subvolcanic reservoir of Kerimasi Volcano in the East African Rift. Trace element concentrations of silicate and carbonate melt inclusions trapped in nepheline, apatite and magnetite from plutonic afrikandite (clinopyroxene-nepheline-perovskite-magnetite-melilite rock) and calciocarbonatite (calcite-apatite-magnetite-perovskite-monticellite-phlogopite rock) show that liquid immiscibility occurred during the generation of carbonatite magmas from a CO2-rich melilite-nephelinite magma formed at relatively high temperatures (1,100 °C). This carbonatite magma is notably more calcic and less alkaline than that occurring at Oldoinyo Lengai. The CaO-rich (32-41 wt%) nature and alkali-"poor" (at least 7-10 wt% Na2O + K2O) nature of these high-temperature (>1,000 °C) carbonate melts result from strong partitioning of Ca (relative to Mg, Fe and Mn) in the immiscible carbonate and the CaO-rich nature (12-17 wt%) of its silicate parent (e.g., melilite-nephelinite). Evolution of the Kerimasi carbonate magma can result in the formation of natrocarbonatite melts with similar composition to those of Oldoinyo Lengai, but with pronounced depletion in REE and HFSE elements. We suggest that this compositional difference results from the different initial parental magmas, e.g., melilite-nephelinite at Kerimasi and a nephelinite at Oldoinyo Lengai. The difference in parental magma composition led to a significant difference in the fractionating mineral phase assemblage and the element partitioning systematics upon silicate-carbonate melt immiscibility. LA-ICP-MS analysis of coeval silicate and carbonate melt inclusions provides an opportunity to infer carbonate melt/silicate melt partition coefficients for a wide range of elements. These data show that Li, Na, Pb, Ca, Sr, Ba, B, all REE (except Sc), U, V, Nb, Ta, P, Mo, W and S are partitioned into the carbonate

Drilling Magma for Science, Volcano Monitoring, and Energy

Science.gov (United States)

Eichelberger, J. C.; Lavallée, Y.; Blankenship, D.

2017-12-01

Magma chambers are central to understanding magma evolution, formation of continental crust, volcanism, and renewal of hydrothermal systems. Information from geology, petrology, laboratory experiments, and geophysical imagery has led to little consensus except a trend to see magma systems as being crystal-dominant (mush) rather than melt dominant. At high melt viscosities, crystal-liquid fractionation may be achieved by separation of melt from mush rather than crystals from liquid suspension. That the dominant volume has properties more akin to solid than liquid might explain the difficulty in detecting magma geophysically. Recently, geothermal drilling has intersected silicic magma at the following depths and SiO2 contents are: Puna, Hawaii, 2.5 km, 67 wt%; Menengai, Kenya 2.1 km, 67 wt%; Krafla, Iceland, 2.1 km, 75 wt%. Some similarities are: 1) Drillers encountered a "soft", sticky formation; 2) Cuttings or chips of clear quenched glass were recovered; 3) The source of the glass flowed up the well; 4) Transition from solid rock to recovering crystal-poor glass occurred in tens of meters, apparently without an intervening mush zone. Near-liquidus magma at the roof despite rapid heat loss there presents a paradox that may be explained by very recent intrusion of magma, rise of liquidus magma to the roof replacing partially crystallized magma, or extremely skewed representation of melt over mush in cuttings (Carrigan et al, this session). The latter is known to occur by filter pressing of ooze into lava lake coreholes (Helz, this session), but cannot be verified in actual magma without coring. Coring to reveal gradients in phase composition and proportions is required for testing any magma chamber model. Success in drilling into and controlling magma at all three locations, in coring lava lakes to over 1100 C, and in numerical modeling of coring at Krafla conditions (Su, this session) show this to be feasible. Other unprecedented experiments are using the known

Methylated silicates may explain the release of chlorinated methane from Martian soil

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Bak, Ebbe N.; Jensen, Svend J. Knak; Nørnberg, Per; Finster, Kai

2016-01-01

The only organic compounds that have been detected in the Martian soil are simple chlorinated compounds released from heated surface material. However, the sources of the organic carbon are in dispute. Wind abraded silicates, which are widespread on the Martian surface, can sequester atmospheric methane which generates methylated silicates and thus could provide a mechanism for accumulation of reduced carbon in the surface soil. In this study we show that thermal volatilization of methylated silicates in the presence of perchlorate leads to the production of chlorinated methane. Thus, methylated silicates could be a source of the organic carbon released as chlorinated methane upon thermal volatilization of Martian soil samples. Further, our experiments show that the ratio of the different chlorinated compounds produced is dependent on the mass ratio of perchlorate to organic carbon in the soil.

Loki Patera: A Magma Sea Story

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Veeder, G. J.; Matson, D. L.; Rathbun, A. G.

2005-01-01

We consider Loki Patera on Io as the surface expression of a large uniform body of magma. Our model of the Loki magma sea is some 200 km across; larger than a lake but smaller than an ocean. The depth of the magma sea is unknown, but assumed to be deep enough that bottom effects can be ignored. Edge effects at the shore line can be ignored to first order for most of the interior area. In particular, we take the dark material within Loki Patera as a thin solidified lava crust whose hydrostatic shape follows Io's isostatic surface (approx. 1815 km radius of curvature). The dark surface of Loki appears to be very smooth on both regional and local (subresolution) scales. The thermal contrast between the low and high albedo areas within Loki is consistent with the observed global correlation. The composition of the model magma sea is basaltic and saturated with dissolved SO2 at depth. Its average, almost isothermal, temperature is at the liquidus for basalt. Additional information is included in the original extended abstract.

Controls on the organization of the plumbing system of subduction volcanoes : the roles of volatiles and edifice load

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Roman, A. M.; Bergal-Kuvikas, O.; Shapiro, N.; Taisne, B.; Gordeev, E.; Jaupart, C. P.

2017-12-01

Geochemical data indicate that subduction zone magmas are extracted from the mantle and rises through the crust, with a wide range of volatile contents. The main controls on magma ascent, storage and location of eruptive vents are not well understood. Flow through a volcanic system depends on magma density and viscosity, which depend in turn on chemical composition and volatile content. Thus, one expects that changes of eruption sites in space and time are related to geochemical variations. To test this hypothesis, we have focussed on Klyuchevskoy volcano, Kamchatka, a very active island arc volcano which erupts lavas with a wide range of volatile contents (e.g. 3-7 H20 wt. %). The most primitive high-Mg magmas were able to erupt and build a sizable edifice in an initial phase of activity. As the edifice grew, eruption of these magmas was suppressed in the focal area and occurred in distal parts of the volcano whilst summit eruptions involved differentiated high alumina basalts. Here we propose a new model for the development of the Klyuchevskoy plumbing system which combines edifice load, far field tectonic stress and the presence of volatiles. We calculate dyke trajectories and overpressures by taking into account the exsolution of volatiles in the magma. The most striking result is the progressive deflection of dykes towards the axial area as the edifice size increases. In this model, the critical parameters are the depth of volatile exsolution and the edifice size. Volatile-rich magmas degas at depth and experience a large increase in buoyancy which may overcome edifice-induced stresses at shallow levels. However, as the volcano grows, the stress barrier migrates downwards and may eventually act to stall dykes before gas exsolution takes place. Such conditions are likely to induce the formation of a shallow central reseroir, in which further magma focussing, mixing and contamination may take place. This model accounts for the co-evolution of magma composition

Iron Redox Systematics of Shergottites and Martian Magmas

Science.gov (United States)

Righter, Kevin; Danielson, L. R.; Martin, A. M.; Newville, M.; Choi, Y.

2010-01-01

Martian meteorites record a range of oxygen fugacities from near the IW buffer to above FMQ buffer [1]. In terrestrial magmas, Fe(3+)/ SigmaFe for this fO2 range are between 0 and 0.25 [2]. Such variation will affect the stability of oxides, pyroxenes, and how the melt equilibrates with volatile species. An understanding of the variation of Fe(3+)/SigmaFe for martian magmas is lacking, and previous work has been on FeO-poor and Al2O3-rich terrestrial basalts. We have initiated a study of the iron redox systematics of martian magmas to better understand FeO and Fe2O3 stability, the stability of magnetite, and the low Ca/high Ca pyroxene [3] ratios observed at the surface.

Rapid ascent of rhyolitic magma at Chaitén volcano, Chile.

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Castro, Jonathan M; Dingwell, Donald B

2009-10-08

Rhyolite magma has fuelled some of the Earth's largest explosive volcanic eruptions. Our understanding of these events is incomplete, however, owing to the previous lack of directly observed eruptions. Chaitén volcano, in Chile's northern Patagonia, erupted rhyolite magma unexpectedly and explosively on 1 May 2008 (ref. 2). Chaitén residents felt earthquakes about 24 hours before ash fell in their town and the eruption escalated into a Plinian column. Although such brief seismic forewarning of a major explosive basaltic eruption has been documented, it is unprecedented for silicic magmas. As precursory volcanic unrest relates to magma migration from the storage region to the surface, the very short pre-eruptive warning at Chaitén probably reflects very rapid magma ascent through the sub-volcanic system. Here we present petrological and experimental data that indicate that the hydrous rhyolite magma at Chaitén ascended very rapidly, with velocities of the order of one metre per second. Such rapid ascent implies a transit time from storage depths greater than five kilometres to the near surface in about four hours. This result has implications for hazard mitigation because the rapidity of ascending rhyolite means that future eruptions may provide little warning.

The partitioning of barium and lead between silicate melts and aqueous fluids at high pressures and temperatures

International Nuclear Information System (INIS)

Bureau, Helene; Menez, Benedicte; Khodja, Hicham; Daudin, Laurent; Gallien, Jean-Paul; Massare, Dominique; Shaw, Cliff; Metrich, Nicole

2003-01-01

The origin of subduction-related magmas is still a matter of debate in the Earth Sciences. These magmas are characterised by their distinctive trace element compositions compared to magmas from other tectonic settings, e.g. mid-ocean ridges or rifts. The distinct trace element composition of these magmas is generally attributed to alteration of the source region by a contaminating agent: either a silicate melt or a hydrous fluid, possibly chlorine-enriched. In this study, we have used μPIXE (proton induced X-ray emission) to analyse synthetic samples obtained from a micro-experimental petrology study that aims to determine the partitioning behaviour of two key elements, Ba and Pb, between silicate melt and both pure water and saline fluids. Our experiments were performed at high-pressure (>0.34-1.53 GPa) and high-temperature (697-1082 deg. C) in a hydrothermal diamond anvil cell, that was used as a transparent rapid quench autoclave. We observed that at high pressure and temperature, in the presence of pure water, Ba and Pb are not strongly fractionated into one phase or the other. The partition coefficient of Pb is ranging from 0.46 to 1.28. Results from one experiment performed at 0.83 GPa and 847 deg. C, in the presence of a saline fluid indicate that the presence of Cl induces strong fractionation of Pb and moderate fractionation of Ba both into the silicate melt. In addition, our data indicate that Cl is strongly partitioned into the fluid phase

Isotopic patterns in silicic ignimbrites and lava flows of the Mogan and lower Fataga Formations, Gran Canaria, Canary Islands

International Nuclear Information System (INIS)

Cousens, B.L.; Tilton, G.R.; Spera, F.J.

1990-01-01

We report the Sr, Pb, and Nd isotopic composition of thirty-six intercalated extracaldera silicic ignimbrites and basaltic lavas of the Miocene Hogarzales, Mogan, and Fataga Formations, Gran Canaria, Canary Islands. The aims are to constrain petrogenetic models for the silicic volcanics, and determine mantle source characteristics and temporal variations between 14.2 and ≅ 12.1 Ma. Feldspars from the extracaldera silicic ignimbrites are identical in isotopic composition to coeval extracaldera basaltic lavas, supporting a fractional crystallization model for the evolved lavas from parental Hogarzales basalts. 87 Sr/ 86 Sr ratios range from 0.70306 to 0.70341, 206 Pb/ 204 Pb from 19.32 to 19.90, 207 Pb/ 204 Pb from 15.56 to 15.65, and 208 Pb/ 204 Pb from 38.82 to 39.65. 143 Nd/ 144 Nd ratios are nearly constant at 0.512913±15. The source of Gran Canaria magmas is heterogeneous on small scales of both time and distance. Isotope-isotope and isotope-incompatible element plots suggest mixing between well-mixed, slightly enriched mantle (similar to PREMA as defined by Zindler and Hart) and the HIMU mantle component. The proportion of HIMU component (low 87 Sr/ 86 Sr, high 206 Pb/ 204 Pb) increases upsection. Stratigraphic patterns in major, trace element, and isotopic compositions may be explained by the influx of a geochemically distinct ''Fataga'' magma into the Tejeda magma chamber, which mixed with and/or finally completely displaced existing ''Lower Mogan'' magmas. Alternatively, mixing of these two end members could occur in the mantle, prior to injection into the chamber. There is no evidence of lithospheric/asthenospheric contamination in the late-stage shield magmas on Gran Canaria. (orig.)

Production and Preservation of Sulfide Layering in Mercury's Magma Ocean

Science.gov (United States)

Boukare, C.-E.; Parman, S. W.; Parmentier, E. M.; Anzures, B. A.

2018-05-01

Mercury's magma ocean (MMO) would have been sulfur-rich. At some point during MMO solidification, it likely became sulfide saturated. Here we present physiochemical models exploring sulfide layer formation and stability.

Permeability During Magma Expansion and Compaction

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Gonnermann, Helge. M.; Giachetti, Thomas; Fliedner, Céline; Nguyen, Chinh T.; Houghton, Bruce F.; Crozier, Joshua A.; Carey, Rebecca J.

2017-12-01

Plinian lapilli from the 1060 Common Era Glass Mountain rhyolitic eruption of Medicine Lake Volcano, California, were collected and analyzed for vesicularity and permeability. A subset of the samples were deformed at a temperature of 975°, under shear and normal stress, and postdeformation porosities and permeabilities were measured. Almost all undeformed samples fall within a narrow range of vesicularity (0.7-0.9), encompassing permeabilities between approximately 10-15 m2 and 10-10 m2. A percolation threshold of approximately 0.7 is required to fit the data by a power law, whereas a percolation threshold of approximately 0.5 is estimated by fitting connected and total vesicularity using percolation modeling. The Glass Mountain samples completely overlap with a range of explosively erupted silicic samples, and it remains unclear whether the erupting magmas became permeable at porosities of approximately 0.7 or at lower values. Sample deformation resulted in compaction and vesicle connectivity either increased or decreased. At small strains permeability of some samples increased, but at higher strains permeability decreased. Samples remain permeable down to vesicularities of less than 0.2, consistent with a potential hysteresis in permeability-porosity between expansion (vesiculation) and compaction (outgassing). We attribute this to retention of vesicle interconnectivity, albeit at reduced vesicle size, as well as bubble coalescence during shear deformation. We provide an equation that approximates the change in permeability during compaction. Based on a comparison with data from effusively erupted silicic samples, we propose that this equation can be used to model the change in permeability during compaction of effusively erupting magmas.

Magma Fertility is the First-Order Factor for the Formation of Porphyry Cu±Au Deposits

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Park, J. W.; Campbell, I. H.; Malaviarachchi, S. P. K.; Cocker, H.; Nakamura, E.; Kay, S. M.

2017-12-01

Magma fertility, the metal abundance in magma, has been considered to be one of the key factors for the formation of porphyry Cu±Au deposits. In this study we provide clear evidence to support the hypothesis that the platinum group element (PGE) can be used to distinguish barren from ore-bearing Cu±Au felsic suites. We determined the PGE contents of three barren volcanic and subvolcanic suites from Argentina and Japan, and compare the results with two porphyry Cu-bearing subvolcanic suites from Chile and two porphyry Cu-Au-bearing suites from Australia. The barren suites are significantly depleted in PGE abundances by the time of fluid exsolution, which is attributed to early sulfide saturation at mid to lower crust depths or assimilation of chalcophile element-poor crustal materials. Barren magma, produced by melting continental crust, may have been initially deficient in chalcophile elements. In contrast, the Cu±Au ore-bearing suites contain at least an order of magnitude higher PGE contents than those of the barren suites by the time of fluid saturation. They are characterized by late sulfide saturation in a shallow magma chamber, which allows the chalcophile elements to concentrate in the fractionating magma from which they are sequestered by ore-forming fluids. We suggest the Pd/MgO and Pd/Pt ratios of igneous rocks can be used as magma fertility indicators, and to distinguish between barren, porphyry Cu and porphyry Cu-Au magmatic systems.

The roles of fractional crystallization, magma mixing, crystal mush remobilization and volatile-melt interactions in the genesis of a young basalt-peralkaline rhyolite suite, the greater Olkaria volcanic complex, Kenya Rift valley

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Macdonald, R.; Belkin, H.E.; Fitton, J.G.; Rogers, N.W.; Nejbert, K.; Tindle, A.G.; Marshall, A.S.

2008-01-01

The Greater Olkaria Volcanic Complex is a young (???20 ka) multi-centred lava and dome field dominated by the eruption of peralkaline rhyolites. Basaltic and trachytic magmas have been erupted peripherally to the complex and also form, with mugearites and benmoreites, an extensive suite of magmatic inclusions in the rhyolites. The eruptive rocks commonly represent mixed magmas and the magmatic inclusions are themselves two-, three- or four-component mixes. All rock types may carry xenocrysts of alkali feldspar, and less commonly plagioclase, derived from magma mixing and by remobilization of crystal mushes and/or plutonic rocks. Xenoliths in the range gabbro-syenite are common in the lavas and magmatic inclusions, the more salic varieties sometimes containing silicic glass representing partial melts and ranging in composition from anorthite ?? corundum- to acmite-normative. The peralkaline varieties are broadly similar, in major element terms, to the eruptive peralkaline rhyolites. The basalt-trachyte suite formed by a combination of fractional crystallization, magma mixing and resorption of earlier-formed crystals. Matrix glass in metaluminous trachytes has a peralkaline rhyolitic composition, indicating that the eruptive rhyolites may have formed by fractional crystallization of trachyte. Anomalous trace element enrichments (e.g. ??? 2000 ppm Y in a benmoreite) and negative Ce anomalies may have resulted from various Na- and K-enriched fluids evolving from melts of intermediate composition and either being lost from the system or enriched in other parts of the reservoirs. A small group of nepheline-normative, usually peralkaline, magmatic inclusions was formed by fluid transfer between peralkaline rhyolitic and benmoreitic magmas. The plumbing system of the complex consists of several independent reservoirs and conduits, repeatedly recharged by batches of mafic magma, with ubiquitous magma mixing. ?? The Author 2008. Published by Oxford University Press. All

Short-circuiting magma differentiation from basalt straight to rhyolite?

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Ruprecht, P.; Winslow, H.

2017-12-01

Silicic magmas are the product of varying degrees of crystal fractionation and crustal assimilation/melting. Both processes lead to differentiation that is step-wise rather than continuous for example during melt separation from a crystal mush (Dufek and Bachmann, 2010). However, differentiation is rarely efficient enough to evolve directly from a basaltic to a rhyolitic magma. At Volcán Puyehue-Cordón Caulle, Chile, the magma series is dominated by crystal fractionation where mixing trends between primitive and felsic end members in the bulk rock compositions are almost absent (e.g. P, FeO, TiO2 vs. SiO2). How effective fraction is in this magmatic system is not well-known. The 2011-12 eruption at Cordón Caulle provides new constraints that rhyolitic melts may be derived directly from a basaltic mush. Minor, but ubiquitous mafic, crystal-rich enclaves co-erupted with the predominantly rhyolitic near-aphyric magma. These enclaves are among the most primitive compositions erupted at Puyehue-Cordón Caulle and geochemically resemble closely basaltic magmas that are >10 ka old (Singer et al. 2008) and that have been identified as a parental tholeiitic mantle-derived magma (Schmidt and Jagoutz, 2017) for the Southern Andean Volcanic Zone. The vesiculated nature, the presence of a microlite-rich groundmass, and a lack of a Eu anomaly in these encalves suggest that they represent recharge magma/mush rather than sub-solidus cumulates and therefore have potentially a direct petrogenetic link to the erupted rhyolites. Our results indicate that under some conditions crystal fractionation can be very effective and the presence of rhyolitic magmas does not require an extensive polybaric plumbing system. Instead, primitive mantle-derived magmas source directly evolved magmas. In the case, of the magma system beneath Puyehue-Cordón Caulle, which had three historic rhyolitic eruptions (1921-22, 1960, 2011-12) these results raise the question whether rhyolite magma extraction

Apatite: A New Tool For Understanding The Temporal Variability Of Magmatic Volatile Contents

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Stock, M. J.; Humphreys, M.; Smith, V.; Pyle, D. M.; Isaia, R.

2015-12-01

The apatite crystal structure is capable of incorporating H2O, F and Cl, as well as trace CO2 and sulphur. These can be related to parental magma compositions through application of a series of pressure and temperature-dependent exchange reactions (Piccoli and Candela, 1994), permitting apatite crystals to preserve a record of all major volatile species in the melt. Furthermore, due to the general incompatibility of P in other rock-forming minerals, apatite is ubiquitous in igneous systems and often begins crystallising early, such that apatite inclusions within phenocrysts record melt volatile contents throughout magmatic differentiation. In this work, we compare the compositions of apatite inclusions and microphenocrysts with pyroxene-hosted melt inclusions from the Astroni 1 eruption of Campi Flegrei, Italy. These data are coupled with magmatic differentiation models (Gualda et al., 2012), experimental volatile solubility data (Webster et al., 2014) and thermodynamic models of apatite compositional variations (Piccoli and Candela, 1994) to determine a time-series of magmatic volatile evolution in the build-up to eruption. We find that apatite halogen/OH ratios decreased through magmatic differentiation, while melt inclusion F and Cl concentrations increased. Melt inclusion H2O contents are constant at ~2.5 wt%. These data are best explained by volatile-undersaturated differentiation over most of the crystallisation history of the Astroni 1 melt, with melt inclusion H2O contents reset during ascent, due to rapid H diffusion through the phenocryst hosts (Woods et al., 2000). Given the rapid diffusivity of volatiles in apatite (Brenan, 1993), preservation of undersaturated compositions in microphenocrysts suggests that saturation was only achieved a few days to months before eruption and that it may have been the transition into a volatile-saturated state that ultimately triggered eruption. Piccoli and Candela, 1994. Am. J. of Sc., 294, 92-135. Gualda et al., 2012

Modeling Magma Mixing: Evidence from U-series age dating and Numerical Simulations

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Philipp, R.; Cooper, K. M.; Bergantz, G. W.

2007-12-01

Magma mixing and recharge is an ubiquitous process in the shallow crust, which can trigger eruption and cause magma hybridization. Phenocrysts in mixed magmas are recorders for magma mixing and can be studied by in- situ techniques and analyses of bulk mineral separates. To better understand if micro-textural and compositional information reflects local or reservoir-scale events, a physical model for gathering and dispersal of crystals is necessary. We present the results of a combined geochemical and fluid dynamical study of magma mixing processes at Volcan Quizapu, Chile; two large (1846/47 AD and 1932 AD) dacitic eruptions from the same vent area were triggered by andesitic recharge magma and show various degrees of magma mixing. Employing a multiphase numerical fluid dynamic model, we simulated a simple mixing process of vesiculated mafic magma intruded into a crystal-bearing silicic reservoir. This unstable condition leads to overturn and mixing. In a second step we use the velocity field obtained to calculate the flow path of 5000 crystals randomly distributed over the entire system. Those particles mimic the phenocryst response to the convective motion. There is little local relative motion between silicate liquid and crystals due to the high viscosity of the melts and the rapid overturn rate of the system. Of special interest is the crystal dispersal and gathering, which is quantified by comparing the distance at the beginning and end of the simulation for all particle pairs that are initially closer than a length scale chosen between 1 and 10 m. At the start of the simulation, both the resident and new intruding (mafic) magmas have a unique particle population. Depending on the Reynolds number (Re) and the chosen characteristic length scale of different phenocryst-pairs, we statistically describe the heterogeneity of crystal populations on the thin section scale. For large Re (approx. 25) and a short characteristic length scale of particle

Metal-Silicate-Sulfide Partitioning of U, Th, and K: Implications for the Budget of Volatile Elements in Mercury

Science.gov (United States)

Habermann, M.; Boujibar, A.; Righter, K.; Danielson, L.; Rapp, J.; Righter, M.; Pando, K.; Ross, D. K.; Andreasen, R.

2016-01-01

During formation of the solar system, the Sun produced strong solar winds, which stripped away a portion of the volatile elements from the forming planets. Hence, it was expected that planets closest to the sun, such as Mercury, are more depleted in volatile elements in comparison to other terrestrial planets. However, the MESSENGER mission detected higher than expected K/U and K/Th ratios on Mercury's surface, indicating a volatile content between that of Mars and Earth. Our experiments aim to resolve this discrepancy by experimentally determining the partition coefficients (D(sup met/sil)) of K, U, and Th between metal and silicate at varying pressure (1 to 5 GPa), temperature (1500 to 1900 C), oxygen fugacity (IW-2.5 to IW-6.5) and sulfur-content in the metal (0 to 33 wt%). Our data show that U, Th, and K become more siderophile with decreasing fO2 and increasing sulfur-content, with a stronger effect for U and Th in comparison to K. Using these results, the concentrations of U, Th, and K in the bulk planet were calculated for different scenarios, where the planet equilibrated at a fO2 between IW-4 and IW-7, assuming the existence of a FeS layer, between the core and mantle, with variable thickness. These models show that significant amounts of U and Th are partitioned into Mercury's core. The elevated superficial K/U and K/Th values are therefore only a consequence of the sequestration of U and Th into the core, not evidence of the overall volatile content of Mercury.

Phenomena associated with magma expansion into a drift

International Nuclear Information System (INIS)

Gaffney, E.S.

2002-01-01

One of the significant threats to the proposed Yucca Mountain nuclear waste repository has been identified as the possibility of intersection of the underground structure by a basaltic intrusion. Based on the geology of the region, it is assumed that such an intrusion would consist of an alkali basalt similar to the nearby Lathrop Wells cone, which has been dated at about 78 ka. The threat of radioactive release may be either from eruption through the surface above the repository of basalt that had been contaminated or from migration through ground water of radionucleides released as a result of damage to waste packages that interact with the magma. As part of our study of these threats, we are analyzing the phenomena associated with magma expansion into drifts in tuff. The early phenomena of the encounter of volatile-rich basaltic magma with a drift are discussed here.

Seismic tremors and magma wagging during explosive volcanism.

Science.gov (United States)

Jellinek, A Mark; Bercovici, David

2011-02-24

Volcanic tremor is a ubiquitous feature of explosive eruptions. This oscillation persists for minutes to weeks and is characterized by a remarkably narrow band of frequencies from about 0.5 Hz to 7 Hz (refs 1-4). Before major eruptions, tremor can occur in concert with increased gas flux and related ground deformation. Volcanic tremor is thus of particular value for eruption forecasting. Most models for volcanic tremor rely on specific properties of the geometry, structure and constitution of volcanic conduits as well as the gas content of the erupting magma. Because neither the initial structure nor the evolution of the magma-conduit system will be the same from one volcano to the next, it is surprising that tremor characteristics are so consistent among different volcanoes. Indeed, this universality of tremor properties remains a major enigma. Here we employ the contemporary view that silicic magma rises in the conduit as a columnar plug surrounded by a highly vesicular annulus of sheared bubbles. We demonstrate that, for most geologically relevant conditions, the magma column will oscillate or 'wag' against the restoring 'gas-spring' force of the annulus at observed tremor frequencies. In contrast to previous models, the magma-wagging oscillation is relatively insensitive to the conduit structure and geometry, which explains the narrow band of tremor frequencies observed around the world. Moreover, the model predicts that as an eruption proceeds there will be an upward drift in both the maximum frequency and the total signal frequency bandwidth, the nature of which depends on the explosivity of the eruption, as is often observed.

El Hierro's floating stones as messengers of crust-magma interaction at depth

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Burchardt, S.; Troll, V. R.; Schmeling, H.; Koyi, H.; Blythe, L. S.; Longpré, M. A.; Deegan, F. M.

2012-04-01

During the early stages of the submarine eruption that started on October 10 2011 south of El Hierro, Canary Islands, Spain, peculiar eruption products were found floating on the sea surface. These centimetre- to decimetre-sized "bombs" have been termed "restingolites" after the nearby village La Restinga and consist of a basaltic rind and a white to light grey core that resembles pumice in texture. According to Troll et al. (2011; see also Troll et al. EGU 2012 Abstracts), this material consists of a glassy matrix hosting extensive vesicle networks, which results in extremely low densities allowing these rocks to float on sea water. Mineralogical and geochemical analyses reveal that the "restingolites" originate from the sedimentary rocks (sand-, silt-, and mudstones) that form layer 1 of the oceanic crust beneath El Hierro. During the onset and early stages of the eruption, magma ponded at the base of this sedimentary sequence, breaking its way through the sedimentary rocks to the ocean floor. The textures of the "restingolites" reveal that crust-magma interaction during fragmentation and transport of the xenoliths involved rapid partial melting and volatile exsolution. Xenoliths strikingly similar to those from El Hierro are known from eruptions on other Canary Islands (e.g. La Palma, Gran Canaria, and Lanzarote). In fact, they resemble in texture xenoliths of various protoliths from volcanic areas worldwide (e.g. Krakatao, Indonesia, Cerro Quemado, Guatemala, Laacher See, Germany). This indicates that the process of partial melting and volatile exsolution, which the "restingolites" bear witness of, is probably occurring frequently during shallow crustal magma emplacement. Thermomechanical numerical models of the effect of the density decrease associated with the formation of vesicle networks in partially molten xenoliths show that xenoliths of crustal rocks initially sink in a magma chamber, but may start to float to the chamber roof once they start to heat up

Magma flow instability and cyclic activity at soufriere hills volcano, montserrat, british west indies

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Voight; Sparks; Miller; Stewart; Hoblitt; Clarke; Ewart; Aspinall; Baptie; Calder; Cole; Druitt; Hartford; Herd; Jackson; Lejeune; Lockhart; Loughlin; Luckett; Lynch; Norton; Robertson; Watson; Watts; Young

1999-02-19

Dome growth at the Soufriere Hills volcano (1996 to 1998) was frequently accompanied by repetitive cycles of earthquakes, ground deformation, degassing, and explosive eruptions. The cycles reflected unsteady conduit flow of volatile-charged magma resulting from gas exsolution, rheological stiffening, and pressurization. The cycles, over hours to days, initiated when degassed stiff magma retarded flow in the upper conduit. Conduit pressure built with gas exsolution, causing shallow seismicity and edifice inflation. Magma and gas were then expelled and the edifice deflated. The repeat time-scale is controlled by magma ascent rates, degassing, and microlite crystallization kinetics. Cyclic behavior allows short-term forecasting of timing, and of eruption style related to explosivity potential.

INTERACTIONS BETWEEN GABBROID AND GRANITOID MAGMAS DURING FORMATION OF THE PREOBRAZHENSKY INTRUSION, EAST KAZAKHSTAN

Directory of Open Access Journals (Sweden)

S. V. Khromykh

2017-01-01

Full Text Available The paper reports on studies of the Preobrazhensky gabbro‐granitoid intrusion, East Kazakhstan, com‐ posed of the rocks that belong to four phases of intrusion, from quartz monzonites and gabbroids to granite‐ leucogranites. Specific relationships between basite and granitoid rocks are usually classified as the result of interac‐ tions and mixing of liquid magmas, i.e. magma mingling and mixing. Basite rocks are represented by a series from biotite gabbros to monzodiorites. Granitoids rocks are biotite‐amphibole granites. Porphyric granosyenites, com‐ bining the features of both granites and monzodiorites, are also involved in mingling. It is established that the primary granitoid magmas contained granosyenite/quartz‐monzonite and occurred in the lower‐medium‐crust conditions in equilibrium with the garnet‐rich restite enriched with plagioclase. Monzodiorites formed during fractionation of the parent gabbroid magma that originated from the enriched mantle source. We propose a magma interaction model describing penetration of the basite magma into the lower horizons of the granitoid source, which ceased below the viscoplastic horizon of granitoids. The initial interaction assumes the thermal effect of basites on the almost crystal‐ lized granitic magma and saturation of the boundary horizons of the basite magma with volatile elements, which can change the composition of the crystallizing melt from gabbroid to monzodiorite. A ‘boundary’ layer of monzodiorite melt is formed at the boundary of the gabbroid and granitoid magmas, and interacts with granitoids. Due to chemical interactions, hybrid rocks – porphyric granosyenites – are formed. The heterogeneous mixture of monzodiorites and granosyenites is more mobile in comparison with the overlying almost crystallized granites. Due to contraction frac‐ turing in the crystallized granites, the heterogeneous mixture of monzodiorites and granosyenites penetrate into the

Siderophile Volatile Element Partitioning during Core Formation.

Science.gov (United States)

Loroch, D. C.; Hackler, S.; Rohrbach, A.; Klemme, S.

2017-12-01

Since the nineteen sixties it is known, that the Earth's mantle is depleted relative to CI chondrite in numerous elements as a result of accretion and core-mantle differentiation. Additionally, if we take the chondritic composition as the initial solar nebular element abundances, the Earth lacks 85 % of K and up to 98 % of other volatiles. However one potentially very important group of elements has received considerably less attention in this context and these elements are the siderophile but volatile elements (SVEs). SVEs perhaps provide important information regarding the timing of volatile delivery to Earth. Especially for the SVEs the partitioning between metal melt and silicate melt (Dmetal/silicate) at core formation conditions is poorly constrained, never the less they are very important for most of the core formation models. This study is producing new metal-silicate partitioning data for a wide range of SVEs (S, Se, Te, Tl, Ag, As, Au, Cd, Bi, Pb, Sn, Cu, Ge, Zn, In and Ga) with a focus on the P, T and fO2dependencies. The initial hypothesis that we are aiming to test uses the accretion of major portions of volatile elements while the core formation was still active. The key points of this study are: - What are the effects of P, T and fO2 on SVE metal-silicate partioning? - What is the effect of compositional complexity on SVE metal-silicate partioning? - How can SVE's D-values fit into current models of core formation? The partitioning experiments will be performed using a Walker type multi anvil apparatus in a pressure range between 10 and 20 GPa and temperatures of 1700 up to 2100 °C. To determine the Dmetal/silicate values we are using a field emission high-resolution JEOL JXA-8530F EPMA for major elements and a Photon Machines Analyte G2 Excimer laser (193 nm) ablation system coupled to a Thermo Fisher Element 2 single-collector ICP-MS (LA-ICP-MS) for the trace elements. We recently finished the first sets of experiments and can provide the

Making Earth's earliest continental crust - an analogue from voluminous Neogene silicic volcanism in NE-Iceland

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Berg, Sylvia E.; Troll, Valentin R.; Burchardt, Steffi; Riishuus, Morten S.; Deegan, Frances M.; Harris, Chris; Whitehouse, Martin J.; Gústafsson, Ludvik E.

2014-05-01

Borgarfjörður Eystri in NE-Iceland represents the second-most voluminous exposure of silicic eruptive rocks in Iceland and is a superb example of bimodal volcanism (Bunsen-Daly gap), which represents a long-standing controversy that touches on the problem of crustal growth in early Earth. The silicic rocks in NE-Iceland approach 25 % of the exposed rock mass in the region (Gústafsson et al., 1989), thus they significantly exceed the usual ≤ 12 % in Iceland as a whole (e.g. Walker, 1966; Jonasson, 2007). The origin, significance, and duration of the voluminous (> 300 km3) and dominantly explosive silicic activity in Borgarfjörður Eystri is not yet constrained (c.f. Gústafsson, 1992), leaving us unclear as to what causes silicic volcanism in otherwise basaltic provinces. Here we report SIMS zircon U-Pb ages and δ18O values from the region, which record the commencement of silicic igneous activity with rhyolite lavas at 13.5 to 12.8 Ma, closely followed by large caldera-forming ignimbrite eruptions from the Breiðavik and Dyrfjöll central volcanoes (12.4 Ma). Silicic activity ended abruptly with dacite lava at 12.1 Ma, defining a ≤ 1 Myr long window of silicic volcanism. Magma δ18O values estimated from zircon range from 3.1 to 5.5 (± 0.3; n = 170) and indicate up to 45 % assimilation of a low-δ18O component (e.g. typically δ18O = 0 ‰, Bindeman et al., 2012). A Neogene rift relocation (Martin et al., 2011) or the birth of an off-rift zone to the east of the mature rift associated with a thermal/chemical pulse in the Iceland plume (Óskarsson & Riishuus, 2013), likely brought mantle-derived magma into contact with fertile hydrothermally-altered basaltic crust. The resulting interaction triggered large-scale crustal melting and generated mixed-origin silicic melts. Such rapid formation of silicic magmas from sustained basaltic volcanism may serve as an analogue for generating continental crust in a subduction-free early Earth (e.g. ≥ 3 Ga, Kamber et

Mantle to surface degassing of alkalic magmas at Erebus volcano, Antarctica

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Oppenheimer, C.; Moretti, R.; Kyle, P.R.; Eschenbacher, A.; Lowenstern, J. B.; Hervig, R.L.; Dunbar, N.W.

2011-01-01

Continental intraplate volcanoes, such as Erebus volcano, Antarctica, are associated with extensional tectonics, mantle upwelling and high heat flow. Typically, erupted magmas are alkaline and rich in volatiles (especially CO2), inherited from low degrees of partial melting of mantle sources. We examine the degassing of the magmatic system at Erebus volcano using melt inclusion data and high temporal resolution open-path Fourier transform infrared (FTIR) spectroscopic measurements of gas emissions from the active lava lake. Remarkably different gas signatures are associated with passive and explosive gas emissions, representative of volatile contents and redox conditions that reveal contrasting shallow and deep degassing sources. We show that this unexpected degassing signature provides a unique probe for magma differentiation and transfer of CO2-rich oxidised fluids from the mantle to the surface, and evaluate how these processes operate in time and space. Extensive crystallisation driven by CO2 fluxing is responsible for isobaric fractionation of parental basanite magmas close to their source depth. Magma deeper than 4kbar equilibrates under vapour-buffered conditions. At shallower depths, CO2-rich fluids accumulate and are then released either via convection-driven, open-system gas loss or as closed-system slugs that ascend and result in Strombolian eruptions in the lava lake. The open-system gases have a reduced state (below the QFM buffer) whereas the closed-system gases preserve their deep oxidised signatures (close to the NNO buffer). ?? 2011 Elsevier B.V.

The decompression of basaltic magma into a sub-surface repository

NARCIS (Netherlands)

Bokhove, Onno; Woods, A.W.

2002-01-01

We examine the ascent of volatile-rich basaltic magma through a vertical dike that intersects a horizontal tunnel of comparable cross-sectional area to the dike and located 300 $m$ below the surface and initially filled with air at atmospheric pressure. This process is a simplified representation of

Sr and Nd isotope geochemistry of coexisting alkaline magma series, Cantal, Massif Central, France

International Nuclear Information System (INIS)

Downes, H.

1984-01-01

Sr and Nd isotope analyses are presented for Tertiary continental alkaline volcanics from Cantal, Massif Central, France. The volcanics belong to two main magma series, silica-saturated and silica-undersaturated (with rare nephelinites). Trace element and isotopic data indicate a common source for the basic parental magmas of both major series; the nephelinites in contrast must have been derived from a mantle source which is isotopically and chemically distinct from that which gave rise to the basalts and basanites. 87 Sr/ 86 Sr initial ratios range from 0.7034 to 0.7056 in the main magma series (excluding rhyolites) and 143 Nd/ 144 Nd ratios vary between 0.512927 and 0.512669; both are correlated with increasing SiO 2 in the lavas. The data can be explained by a model of crustal contamination linked with fractional crystallisation. This indicates that crustal magma chambers are the sites of differentiation since only rarely do evolved magmas not show a crustal isotopic signature and conversely basic magmas have primitive isotopic ratios unless they contain obviuos crustal-derived xenocrysts. Potential contaminants include lower crustal granulites or partial melts of upper crustal units. Equal amounts of contamination are required for both magma series, refuting hypotheses of selective contamination of the silica-saturated series. The isotopic characteristics of the apparently primary nephelinite lavas demonstrates widespread heterogeneity in the mantle beneath Cantal. Some rhyolites, previously thought to be extremely contaminated or to be crustally derived, are shown to have undergone post-emplacement hydrothermal alteration. (orig.)

Silicate Inclusions in IAB Irons: Correlations Between Metal Composition and Inclusion Properties, and Inferences for Their Origin

Science.gov (United States)

Benedix, G. K.; McCoy, T. J.; Keil, K.

1995-09-01

IAB irons are the largest group of iron meteorites, exhibit a large range of siderophile element concentrations in their metal, and commonly contain silicate inclusions with roughly chondritic composition. They are closely related to IIICD irons [1,2] and their inclusions resemble winonaites [3]. It has been suggested that IAB's and IIICD's formed in individual impact melt pools [4,2] on a common parent body. However, it has also been suggested that fractional crystallization [5,6] of a S-saturated core could produce the observed siderophile element trends. Metal composition is correlated with silicate inclusion mineralogy in IIICD's [1], indicating reactions between solid silicates and the metallic magma in a core. These trends observed in IIICD's differ from those in IAB's, suggesting different parent bodies. A bi-modal grouping, based primarily on mineralogy and mineral abundances, was suggested for IAB inclusions [7]. However, recent recoveries of several new silicate-bearing IAB's, along with the emergence of new ideas on their origins, prompted a comprehensive study to document more fully the range of inclusions within IAB irons, to examine possible correlations between the compositions of the metallic host and the silicate inclusions, and to elucidate the origin of IAB irons. We are studying troilite-graphite-silicate inclusions in 24 IAB irons with Ni concentrations ranging from 6.6-25.0%. These include Odessa and Copiapo types [7], newly recovered meteorites (e.g., Lueders [8]) and meteorites with extreme Ni contents (e.g., Jenny's Creek, 6.8%; San Cristobal, 25.0% [9]). The inclusions exhibit a range of textures from recrystallized to partial melts (e.g., Caddo County [10]). Rigorous classification [7] is hampered by heterogeneities between group meteorites, between different samples of distinct meteorites, and within individual inclusions. While intergroup heterogeneities make comparisons between the suite of IAB's somewhat difficult, some general trends

Magma decompression rates during explosive eruptions of Kīlauea volcano, Hawaii, recorded by melt embayments

Science.gov (United States)

Ferguson, David J.; Gonnermann, Helge M.; Ruprecht, Philipp; Plank, Terry; Hauri, Erik H.; Houghton, Bruce F.; Swanson, Donald A.

2016-01-01

The decompression rate of magma as it ascends during volcanic eruptions is an important but poorly constrained parameter that controls many of the processes that influence eruptive behavior. In this study, we quantify decompression rates for basaltic magmas using volatile diffusion in olivine-hosted melt tubes (embayments) for three contrasting eruptions of Kīlauea volcano, Hawaii. Incomplete exsolution of H2O, CO2, and S from the embayment melts during eruptive ascent creates diffusion profiles that can be measured using microanalytical techniques, and then modeled to infer the average decompression rate. We obtain average rates of ~0.05–0.45 MPa s−1 for eruptions ranging from Hawaiian style fountains to basaltic subplinian, with the more intense eruptions having higher rates. The ascent timescales for these magmas vary from around ~5 to ~36 min from depths of ~2 to ~4 km, respectively. Decompression-exsolution models based on the embayment data also allow for an estimate of the mass fraction of pre-existing exsolved volatiles within the magma body. In the eruptions studied, this varies from 0.1 to 3.2 wt% but does not appear to be the key control on eruptive intensity. Our results do not support a direct link between the concentration of pre-eruptive volatiles and eruptive intensity; rather, they suggest that for these eruptions, decompression rates are proportional to independent estimates of mass discharge rate. Although the intensity of eruptions is defined by the discharge rate, based on the currently available dataset of embayment analyses, it does not appear to scale linearly with average decompression rate. This study demonstrates the utility of the embayment method for providing quantitative constraints on magma ascent during explosive basaltic eruptions.

Magma decompression rates during explosive eruptions of Kīlauea volcano, Hawaii, recorded by melt embayments

Science.gov (United States)

Ferguson, David J.; Gonnermann, Helge M.; Ruprecht, Philipp; Plank, Terry; Hauri, Erik H.; Houghton, Bruce F.; Swanson, Donald A.

2016-10-01

The decompression rate of magma as it ascends during volcanic eruptions is an important but poorly constrained parameter that controls many of the processes that influence eruptive behavior. In this study, we quantify decompression rates for basaltic magmas using volatile diffusion in olivine-hosted melt tubes (embayments) for three contrasting eruptions of Kīlauea volcano, Hawaii. Incomplete exsolution of H2O, CO2, and S from the embayment melts during eruptive ascent creates diffusion profiles that can be measured using microanalytical techniques, and then modeled to infer the average decompression rate. We obtain average rates of ~0.05-0.45 MPa s-1 for eruptions ranging from Hawaiian style fountains to basaltic subplinian, with the more intense eruptions having higher rates. The ascent timescales for these magmas vary from around ~5 to ~36 min from depths of ~2 to ~4 km, respectively. Decompression-exsolution models based on the embayment data also allow for an estimate of the mass fraction of pre-existing exsolved volatiles within the magma body. In the eruptions studied, this varies from 0.1 to 3.2 wt% but does not appear to be the key control on eruptive intensity. Our results do not support a direct link between the concentration of pre-eruptive volatiles and eruptive intensity; rather, they suggest that for these eruptions, decompression rates are proportional to independent estimates of mass discharge rate. Although the intensity of eruptions is defined by the discharge rate, based on the currently available dataset of embayment analyses, it does not appear to scale linearly with average decompression rate. This study demonstrates the utility of the embayment method for providing quantitative constraints on magma ascent during explosive basaltic eruptions.

Chemical consequences of compaction within the freezing front of a crystallizing magma ocean

Science.gov (United States)

Hier-Majumder, S.; Hirschmann, M. M.

2013-12-01

The thermal and compositional evolution of planetary magma oceans have profound influences on the early development and differentiation of terrestrial planets. During crystallization, rejection of elements incompatible in precipitating solids leads to petrologic and geochemical planetary differentiation, including potentially development of a compositionally stratified early mantle and evolution of thick overlying atmospheres. In cases of extremely efficient segregation of melt and crystals, solidified early mantles can be nearly devoid of key incompatible species including heat-producing (U, Th, K) and volatile (H,C,N,& noble gas) elements. A key structural component of a crystallizing magma ocean is the partially molten freezing front. The dynamics of this region influences the distribution of incompatible elements between the earliest mantle and the initial surficial reservoirs. It also can be the locus of heating owing to the dissipation of large amounts of tidal energy potentially available from the early Moon. The dynamics are influenced by the solidification rate, which is coupled to the liberation of volatiles owing to the modulating greenhouse effects in the overlying thick atmosphere. Compaction and melt retention in the freezing front of a magma ocean has received little previous attention. While the front advances during the course of crystallization, coupled conservation of mass, momentum, and energy within the front controls distribution and retention of melt within this layer. Due to compaction within this layer, melt distribution is far from uniform, and the fraction of melt trapped within this front depends on the rate of freezing of the magma ocean. During phases of rapid freezing, high amount of trapped melt within the freezing front retains a larger quantity of dissolved volatiles and the reverse is true during slow periods of crystallization. Similar effects are known from inferred trapped liquid fractions in layered mafic intrusions. Here we

Chlorine as a geobarometer for alkaline magmas: Evidence from a systematic study of the eruptions of Mount Somma-Vesuvius

Science.gov (United States)

Balcone-Boissard, H.; Boudon, G.; Cioni, R.; Webster, J. D.; Zdanowicz, G.; Orsi, G.; Civetta, L.

2016-02-01

Defining the magma storage conditions of a volcanic system is a major goal in modern volcanology due to its direct implications for the style of a possible eruption, and thus on the associated risk of any crisis and the necessary management and mitigation strategies. Below 200 MPa and at equivalent depths, the strongly non-ideal behaviour of the H-C-O-S-Cl-F system in the silicate melt causes unmixing of the fluid phase to form an H2O-rich vapour and a hydrosaline phase in equilibrium with the silicate melt, both responsible for buffering the chlorine (Cl) concentration. Following this equilibrium, the Cl concentration in melts may be used as a geobarometer for alkaline magmas. Systematic application of this method to the main explosive eruptions of Mount Somma-Vesuvius highlights two main magma ponding zones, at ~180-200 and ~100 MPa. At these pressures, the maximum pre-eruptive H2O contents for the different magma compositions can be estimated; the results obtained, largely in agreement with the current literature, therefore confirm the validity of the method. The Cl geobarometer may help scientists to define the variation of the magmatic reservoir location through time and thus provide strong constraints on pre-eruptive conditions, which are of utmost importance for volcanic crisis management.

Aleutian tholeiitic and calc-alkaline magma series I: The mafic phenocrysts

Science.gov (United States)

Kay, S. Mahlburg; Kay, Robert W.

1985-07-01

Diagnostic mafic silicate assemblages in a continuous spectrum of Aleutian volcanic rocks provide evidence for contrasts in magmatic processes in the Aleutian arc crust. Tectonic segmentation of the arc exerts a primary control on the variable mixing, fractional crystallization and possible assimilation undergone by the magmas. End members of the continuum are termed calc-alkaline (CA) and tholeiitic (TH). CA volcanic rocks (e.g., Buldir and Moffett volcanoes) have low FeO/MgO ratios and contain compositionally diverse phenocryst populations, indicating magma mixing. Their Ni and Cr-rich magnesian olivine and clinopyroxene come from mantle-derived mafic olivine basalts that have mixed with more fractionated magmas at mid-to lower-crustal levels immediately preceding eruption. High-Al amphibole is associated with the mafic end member. In contrast, TH lavas (e.g., Okmok and Westdahl volcanoes) have high FeO/MgO ratios and contain little evidence for mixing. Evolved lavas represent advanced stages of low pressure crystallization from a basaltic magma. These lavas contain groundmass olivine (FO 40 50) and lack Ca-poor pyroxene. Aleutian volcanic rocks with intermediate FeO/MgO ratios are termed transitional tholeiitic (TTH) and calc-alkaline (TCA). TCA magmas are common (e.g., Moffett, Adagdak, Great Sitkin, and Kasatochi volcanoes) and have resulted from mixing of high-Al basalt with more evolved magmas. They contain amphibole (high and low-Al) or orthopyroxene or both and are similar to the Japanese hypersthene-series. TTH magmas (e.g., Okmok and Westdahl) contain orthopyroxene or pigeonite or both, and show some indication of upper crustal mixing. They are mineralogically similar to the Japanese pigeonite-series. High-Al basalt lacks Mg-rich mafic phases and is a derivative magma produced by high pressure fractionation of an olivine tholeiite. The low pressure mineral assemblage of high-Al basalt results from crystallization at higher crustal levels.

Melt inclusion evidence for a volatile-enriched (H2O, Cl, B) component in parental magmas of Gorgona Island komatiites

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Kamenetsky, V.; Sobolev, A.; McDonough, W.

2003-04-01

Late Cretaceous komatiites of Gorgona Island are unambiguous samples of ultra-mafic melts related to a hot and possibly 'wet' mantle plume. Despite significant efforts in studying komatiites, their volatile abundances remain largely unknown because of significant alteration of rocks and lack of fresh glasses. This work presents major, trace and volatile element data for 22 partially homogenised (at 1275oC and 1 bar pressure) melt inclusions in olivine (Fo 90.5-91.5) from a Gorgona Isl. komatiite (# Gor 94-3). Major element compositions (except FeO which is notably lower by up to 5 wt% as a result of post-entrapment re-equilibration) and most lithophile trace elements of melt inclusions are indistinguishable from the whole rock komatiites. With the exception of three inclusions that have low Na, H2O, Cl, F and S (likely compromised and degassed during heating) most compositions are characterised by relatively constant and high volatile abundances (H2O 0.4-0.8 wt%, Cl 0.02-0.03 wt%, B 0.8-1.4 ppm). These are interpreted as representative of original volatiles in parental melts because they correspond to the internal volatile pressure in the closed inclusions significantly exceeding 1 bar pressure of heating experiment. Although H2O is strongly enriched (PM-normalised H2O/Ce 10-17) its concentrations correlate well with many elements (e.g. Yb, Er, Y, Ti, Sr, Be). Other positive anomalies on the overall depleted (La/Sm 0.26-0.33) PM normalized compositional spectra of melt inclusions are shown by B (B/K 2.4-5.4) and Cl (Cl/K 11-16). Compositions of melt inclusions, when corrected for Fe loss and recalculated in equilibrium with host olivine, have high MgO (15.4-16.4 wt%; Mg# of 74) and substantial H2O (0.4-0.6 wt%) contents. This together with the data on other 'enriched' elements argues for the presence of previously unknown volatile-enriched component in the parental melts of Gorgona Isl. komatiites. We discuss contamination of magmas by altered oceanic crust in the

NanoSIMS results from olivine-hosted melt embayments: Magma ascent rate during explosive basaltic eruptions

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Lloyd, Alexander S.; Ruprecht, Philipp; Hauri, Erik H.; Rose, William; Gonnermann, Helge M.; Plank, Terry

2014-08-01

The explosivity of volcanic eruptions is governed in part by the rate at which magma ascends and degasses. Because the time scales of eruptive processes can be exceptionally fast relative to standard geochronometers, magma ascent rate remains difficult to quantify. Here we use as a chronometer concentration gradients of volatile species along open melt embayments within olivine crystals. Continuous degassing of the external melt during magma ascent results in diffusion of volatile species from embayment interiors to the bubble located at their outlets. The novel aspect of this study is the measurement of concentration gradients in five volatile elements (CO2, H2O, S, Cl, F) at fine-scale (5-10 μm) using the NanoSIMS. The wide range in diffusivity and solubility of these different volatiles provides multiple constraints on ascent timescales over a range of depths. We focus on four 100-200 μm, olivine-hosted embayments erupted on October 17, 1974 during the sub-Plinian eruption of Volcán de Fuego. H2O, CO2, and S all decrease toward the embayment outlet bubble, while F and Cl increase or remain roughly constant. Compared to an extensive melt inclusion suite from the same day of the eruption, the embayments have lost both H2O and CO2 throughout the entire length of the embayment. We fit the profiles with a 1-D numerical diffusion model that allows varying diffusivities and external melt concentrations as a function of pressure. Assuming a constant decompression rate from the magma storage region at approximately 220 MPa to the surface, H2O, CO2 and S profiles for all embayments can be fit with a relatively narrow range in decompression rates of 0.3-0.5 MPa/s, equivalent to 11-17 m/s ascent velocity and an 8 to 12 minute duration of magma ascent from ~ 10 km depth. A two stage decompression model takes advantage of the different depth ranges over which CO2 and H2O degas, and produces good fits given an initial stage of slow decompression (0.05-0.3 MPa/s) at high

Magma genesis, storage and eruption processes at Aluto volcano, Ethiopia: lessons from remote sensing, gas emissions and geochemistry

Science.gov (United States)

Hutchison, William; Biggs, Juliet; Mather, Tamsin; Pyle, David; Gleeson, Matthew; Lewi, Elias; Yirgu, Gezahgen; Caliro, Stefano; Chiodini, Giovanni; Fischer, Tobias

2016-04-01

One of the most intriguing aspects of magmatism during the transition from continental rifting to sea-floor spreading is that large silicic magmatic systems develop within the rift zone. In the Main Ethiopian Rift (MER) these silicic volcanoes not only pose a significant hazard to local populations but they also sustain major geothermal resources. Understanding the journey magma takes from source to surface beneath these volcanoes is vital for determining its eruption style and for better evaluating the geothermal resources that these complexes host. We investigate Aluto, a restless silicic volcano in the MER, and combine a wide range of geochemical and geophysical techniques to constrain magma genesis, storage and eruption processes and shed light on magmatic-hydrothermal-tectonic interactions. Magma genesis and storage processes at Aluto were evaluated using new whole-rock geochemical data from recent eruptive products. Geochemical modelling confirms that Aluto's peralkaline rhyolites, that constitute the bulk of recent erupted products, are generated from protracted fractionation (>80 %) of basalt that is compositionally similar to rift-related basalts found on the margins of the complex. Crustal melting did not play a significant role in rhyolite genesis and melt storage depths of ~5 km can reproduce almost all aspects of their geochemistry. InSAR methods were then used to investigate magma storage and fluid movement at Aluto during an episode of ground deformation that took place between 2008 and 2010. Combining new SAR imagery from different viewing geometries we identified an accelerating uplift pulse and found that source models support depths of magmatic and/or fluid intrusion at ~5 km for the uplift and shallower depths of ~4 km for the subsidence. Finally, gas samples collected on Aluto in 2014 were used to evaluate magma and fluid transport processes. Our results show that gases are predominantly emanating from major fault zones on Aluto and that they

Isotopic composition of carbon in dacitic gases from Usu volcano (Japan). Relationship between the 13C/12C ratio of volatiles and the 87Sr/86Sr ratio of silicates in arc volcanism

International Nuclear Information System (INIS)

Allard, Patrick

1981-01-01

CO 2 emitted at 568 deg C by the new dacitic intrusion in Usu volcano (Japan) has a 13 C/ 12 C ratio of -4.4 per mill vs PDB. Such a value, together with previous isotopic data from other volcanoes in Japan, Indonesia, Central America, Lesser Antilles and New Zealand, enhance that the carbon released by magmas in subduction zones is systematically 13 C-enriched with respect to the primary carbon from rift areas. Such a 13 C enrichment in volatiles is explained in terms of crustal contamination by sedimentary carbon, and can be sowewhat related to a simultaneous increase of 87 Sr in the magma [fr

Beam depolarization and gain saturation in neodymium rods with a diameter of 85 mm

Energy Technology Data Exchange (ETDEWEB)

Sukhanov, V N; Ugodenko, A A

1990-04-01

Depolarization and gain saturation were investigated in rod amplifiers using phosphate and silicate Nd glasses 85 mm in diameter and 300 mm in length at a pulse duration of 35 ns. Total depolarization losses over the rod cross section were measured for various radial distributions of the small-signal gain. For the phosphate glass the losses amounted to 3-6 percent; for the silicate glass, they amounted to 4-7 percent. Saturation energy densities of 4.5 + or - 0.4 and 8.0 + or - 0.7 J/sq cm were obtained for the phosphate and silicate glass, respectively. 8 refs.

High-temperature apparatus for chaotic mixing of natural silicate melts

Energy Technology Data Exchange (ETDEWEB)

Morgavi, D.; Petrelli, M.; Vetere, F. P.; González-García, D.; Perugini, D., E-mail: diego.perugini@unipg.it [Department of Physics and Geology, Petro-Volcanology Research Group (PVRG), University of Perugia, Piazza Università, Perugia 06100 (Italy)

2015-10-15

A unique high-temperature apparatus was developed to trigger chaotic mixing at high-temperature (up to 1800 °C). This new apparatus, which we term Chaotic Magma Mixing Apparatus (COMMA), is designed to carry out experiments with high-temperature and high-viscosity (up to 10{sup 6} Pa s) natural silicate melts. This instrument allows us to follow in time and space the evolution of the mixing process and the associated modulation of chemical composition. This is essential to understand the dynamics of magma mixing and related chemical exchanges. The COMMA device is tested by mixing natural melts from Aeolian Islands (Italy). The experiment was performed at 1180 °C using shoshonite and rhyolite melts, resulting in a viscosity ratio of more than three orders of magnitude. This viscosity ratio is close to the maximum possible ratio of viscosity between high-temperature natural silicate melts. Results indicate that the generated mixing structures are topologically identical to those observed in natural volcanic rocks highlighting the enormous potential of the COMMA to replicate, as a first approximation, the same mixing patterns observed in the natural environment. COMMA can be used to investigate in detail the space and time development of magma mixing providing information about this fundamental petrological and volcanological process that would be impossible to investigate by direct observations. Among the potentials of this new experimental device is the construction of empirical relationships relating the mixing time, obtained through experimental time series, and chemical exchanges between the melts to constrain the mixing-to-eruption time of volcanic systems, a fundamental topic in volcanic hazard assessment.

High-temperature apparatus for chaotic mixing of natural silicate melts

International Nuclear Information System (INIS)

Morgavi, D.; Petrelli, M.; Vetere, F. P.; González-García, D.; Perugini, D.

2015-01-01

A unique high-temperature apparatus was developed to trigger chaotic mixing at high-temperature (up to 1800 °C). This new apparatus, which we term Chaotic Magma Mixing Apparatus (COMMA), is designed to carry out experiments with high-temperature and high-viscosity (up to 10 6 Pa s) natural silicate melts. This instrument allows us to follow in time and space the evolution of the mixing process and the associated modulation of chemical composition. This is essential to understand the dynamics of magma mixing and related chemical exchanges. The COMMA device is tested by mixing natural melts from Aeolian Islands (Italy). The experiment was performed at 1180 °C using shoshonite and rhyolite melts, resulting in a viscosity ratio of more than three orders of magnitude. This viscosity ratio is close to the maximum possible ratio of viscosity between high-temperature natural silicate melts. Results indicate that the generated mixing structures are topologically identical to those observed in natural volcanic rocks highlighting the enormous potential of the COMMA to replicate, as a first approximation, the same mixing patterns observed in the natural environment. COMMA can be used to investigate in detail the space and time development of magma mixing providing information about this fundamental petrological and volcanological process that would be impossible to investigate by direct observations. Among the potentials of this new experimental device is the construction of empirical relationships relating the mixing time, obtained through experimental time series, and chemical exchanges between the melts to constrain the mixing-to-eruption time of volcanic systems, a fundamental topic in volcanic hazard assessment

Dynamics of a large, restless, rhyolitic magma system at Laguna del Maule, southern Andes, Chile

Science.gov (United States)

Singer, Brad S.; Andersen, Nathan L.; Le Mével, Hélène; Feigl, Kurt L.; DeMets, Charles; Tikoff, Basil; Thurber, Clifford H.; Jicha, Brian R.; Cardonna, Carlos; Córdova, Loreto; Gil, Fernando; Unsworth, Martyn J.; Williams-Jones, Glyn; Miller, Craig W.; Fierstein, Judith; Hildreth, Edward; Vazquez, Jorge A.

2014-01-01

Explosive eruptions of large-volume rhyolitic magma systems are common in the geologic record and pose a major potential threat to society. Unlike other natural hazards, such as earthquakes and tsunamis, a large rhyolitic volcano may provide warning signs long before a caldera-forming eruption occurs. Yet, these signs—and what they imply about magma-crust dynamics—are not well known. This is because we have learned how these systems form, grow, and erupt mainly from the study of ash flow tuffs deposited tens to hundreds of thousands of years ago or more, or from the geophysical imaging of the unerupted portions of the reservoirs beneath the associated calderas. The Laguna del Maule Volcanic Field, Chile, includes an unusually large and recent concentration of silicic eruptions. Since 2007, the crust there has been inflating at an astonishing rate of at least 25 cm/yr. This unique opportunity to investigate the dynamics of a large rhyolitic system while magma migration, reservoir growth, and crustal deformation are actively under way is stimulating a new international collaboration. Findings thus far lead to the hypothesis that the silicic vents have tapped an extensive layer of crystal-poor, rhyolitic melt that began to form atop a magmatic mush zone that was established by ca. 20 ka with a renewed phase of rhyolite eruptions during the Holocene. Modeling of surface deformation, magnetotelluric data, and gravity changes suggest that magma is currently intruding at a depth of ~5 km. The next phase of this investigation seeks to enlarge the sets of geophysical and geochemical data and to use these observations in numerical models of system dynamics.

Fractionation, ascent, and extrusion of magma at the Santiaguito volcanic dome, Guatemala

Science.gov (United States)

Scott, J.; Mather, T. A.; Pyle, D. M.

2011-12-01

The silicic dome complex of Santiaguito, Guatemala has exhibited continuous low-level activity for nearly 90 years[1]. Despite its longevity, remarkably little is known about the magmatic plumbing system beneath Santiaguito. We present preliminary constraints on this system, based on petrological analyses of lava samples. Amphibole thermobarometry suggests magma evolves during slow ascent through a phenocryst fractionation zone - a complex of dikes and sills, extending from at least ~24 km to at most ~12 km beneath Santiaguito. Discontinuous plagioclase size distributions suggest this slow fractionation ends at depth, and degassing-induced crystallization of microlites begins. The texture and geochemistry of microlites is consistent with uninterrupted final ascent; there is no evidence of shallow magma storage beneath Santiaguito. The normative composition of matrix glass, and the morphology and volume of plagioclase microlites suggests ascending magma crosses the rigidification threshold within preserved, and ductile behaviour is replaced by dominantly brittle behaviour, previously referred to as "final melt quench". We suggest rigidification slows the ascent of magma and may create the conduit plug previously observed at Santiaguito[2]. This rigid mass of magma may begin to fracture almost immediately to form a semi-permeable plug, before extruding onto the surface as blocky lava. The extrusion rate may be reflected in the extent of matrix glass decomposition to crystalline silica and alkali feldspar. This preliminary picture of the plumbing system beneath Santiaguito may lead to a greater understanding of the behaviour of this enigmatic volcano, and of the danger it poses to the region. However, our findings raise many further questions about the dynamics within silicic dome-forming systems that need to be addressed if we are to work towards a broad and more universal understanding of similar systems worldwide and the hazards they represent. [1] Rose, W.I., 1972

THE VISCOUS TO BRITTLE TRANSITION IN CRYSTAL- AND BUBBLE-BEARING MAGMAS

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Mattia ePistone

2015-11-01

Full Text Available The transition from viscous to brittle behaviour in magmas plays a decisive role in determining the style of volcanic eruptions. While this transition has been determined for one- or two-phase systems, it remains poorly constrained for natural magmas containing silicic melt, crystals, and gas bubbles. Here we present new experimental results on shear-induced fracturing of three-phase magmas obtained at high-temperature (673-1023 K and high-pressure (200 MPa conditions over a wide range of strain-rates (5·10-6 s-1 to 4·10-3 s-1. During the experiments bubbles are deformed (i.e. capillary number are in excess of 1 enough to coalesce and generate a porous network that potentially leads to outgassing. A physical relationship is proposed that quantifies the critical stress required for magmas to fail as a function of both crystal (0.24 to 0.65 and bubble volume fractions (0.09 to 0.12. The presented results demonstrate efficient outgassing for low crystal fraction ( 0.44 promote gas bubble entrapment and inhibit outgassing. The failure of bubble-free, crystal-bearing systems is enhanced by the presence of bubbles that lower the critical failure stress in a regime of efficient outgassing, while the failure stress is increased if bubbles remain trapped within the crystal framework. These contrasting behaviours have direct impact on the style of volcanic eruptions. During magma ascent, efficient outgassing reduces the potential for an explosive eruption and favours brittle behaviour, contributing to maintain low overpressures in an active volcanic system resulting in effusion or rheological flow blockage of magma at depth. Conversely, magmas with high crystallinity experience limited loss of exsolved gas, permitting the achievement of larger overpressures prior to a potential sudden transition to brittle behaviour, which could result in an explosive volcanic eruption.

Non-traditional stable isotope behaviors in immiscible silica-melts in a mafic magma chamber.

Science.gov (United States)

Zhu, Dan; Bao, Huiming; Liu, Yun

2015-12-01

Non-traditional stable isotopes have increasingly been applied to studies of igneous processes including planetary differentiation. Equilibrium isotope fractionation of these elements in silicates is expected to be negligible at magmatic temperatures (δ(57)Fe difference often less than 0.2 per mil). However, an increasing number of data has revealed a puzzling observation, e.g., the δ(57)Fe for silicic magmas ranges from 0‰ up to 0.6‰, with the most positive δ(57)Fe almost exclusively found in A-type granitoids. Several interpretations have been proposed by different research groups, but these have so far failed to explain some aspects of the observations. Here we propose a dynamic, diffusion-induced isotope fractionation model that assumes Si-melts are growing and ascending immiscibly in a Fe-rich bulk magma chamber. Our model offers predictions on the behavior of non-traditional stable isotope such as Fe, Mg, Si, and Li that are consistent with observations from many A-type granitoids, especially those associated with layered intrusions. Diffusion-induced isotope fractionation may be more commonly preserved in magmatic rocks than was originally predicted.

Magma addition rates in continental arcs: New methods of calculation and global implications

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Ratschbacher, B. C.; Paterson, S. R.

2017-12-01

The transport of mass, heat and geochemical constituents (elements and volatiles) from the mantle to the atmosphere occurs via magma addition to the lithosphere. Calculation of magma addition rates (MARs) in continental arcs based on exposed proportions of igneous arc rocks is complex and rarely consistently determined. Multiple factors influence MAR calculations such as crust versus mantle contributions to magmas, a change in MARs across the arc and with depths throughout the arc crustal column, `arc tempos' with periods of high and low magmatic activity, the loss of previous emplaced arc rocks by subsequent magmatism and return to the mantle, arc migration, variations in the intrusive versus extrusive additions and evolving arc widths and thicknesses during tectonism. All of these factors need to be considered when calculating MARs.This study makes a new attempt to calculate MARs in continental arcs by studying three arc sections: the Famatinian arc, Argentina, the Sierra Nevada batholith, California and the Coast Mountain batholith, Washington and British Columbia. Arcs are divided into fore-arc, main arc and back arc sections and `boxes' with a defined width, length and thickness spanning upper middle and lower crustal levels are assigned to each section. Representative exposed crustal slices for each depth are then used to calculate MARs based on outcrop proportions for each box. Geochemical data is used to infer crustal recycling percentages and total thickness of the arc. Preliminary results show a correlation between MARs, crustal thicknesses and magmatic flare-up durations. For instance, the Famatinian arc shows a strong decrease in MARs between the main arc section (9.4 km3/Ma/arc-km) and the fore-arc (0.61 km3/Ma/arc-km) and back-arc (1.52 km3/Ma/arc-km) regions and an increase in the amount of magmatism with depth.Global MARs over geologic timescales have the potential to investigate mantle melt generation rates and the volatile outgassing contribution

Solubility of reduced C-O-H volatiles in basalt as a function of fCO: Implications for the early Earth, the moon, and Mars

Science.gov (United States)

Armstrong, L. S.; Hirschmann, M. M.

2013-12-01

Magmatic C-O-H volatiles influence the evolution of planetary atmospheres and, when precipitated and stored in solidified mantles, the dynamical evolution of planetary interiors. In the case of the Earth, the fO2 of the mantle near the end of core formation should have been ~IW-2, and subsequently increased to present-day values [1]. In experiments with fO2 ≤ IW, a variety of reduced volatile species have been found dissolved in magmas, including H2, CH4, CO, Fe(CO)5 and possibly Fe(CO)62+. However, there remains significant disagreement regarding the identity and concentrations of these volatiles in natural magmas, as well as their dependencies on intensive variables (T, P, fO2, fCO, fH2)[2-6]. Previous experiments document the importance of CO-related species [2,6], but were conducted over a limited range of fCO and had potentially interfering effects from poorly controlled variations in H2O. We aim to experimentally determine the solubility of C-O-H volatiles in basaltic magmas under reduced, C-saturated conditions while minimizing water content. The relationship between volatile speciation, fO2, and fCO at 1.2 GPa and 1400°C are constrained, laying the groundwork for a more extensive study at a range of conditions relevant to the interiors of the terrestrial planets and the moon. Both MORB and a martian basalt were studied, contained in Pt-C capsules with Fe × Pt × Si metal added to generate reducing conditions and to monitor fO2. A nominal amount of H2O is unavoidable in experimental charges, but was minimized by drying capsules prior to welding. Phase compositions were determined by electron microprobe and volatile concentrations were measured by FTIR spectroscopy. In preliminary experiments with fO2 of IW-0.70 to +1.75 (corresponding to log fCO of 3.3-4.5), H2O and CO2 concentrations as determined by FTIR are 113-13283 and 12-721 ppm, respectively. Most experiments also display a small FTIR peak at 2205 cm-1, whereas the most reduced experiments lack

The stable Cr isotopic compositions of chondrites and silicate planetary reservoirs

Science.gov (United States)

Schoenberg, Ronny; Merdian, Alexandra; Holmden, Chris; Kleinhanns, Ilka C.; Haßler, Kathrin; Wille, Martin; Reitter, Elmar

2016-06-01

The depletion of chromium in Earth's mantle (∼2700 ppm) in comparison to chondrites (∼4400 ppm) indicates significant incorporation of chromium into the core during our planet's metal-silicate differentiation, assuming that there was no significant escape of the moderately volatile element chromium during the accretionary phase of Earth. Stable Cr isotope compositions - expressed as the ‰-difference in 53Cr/52Cr from the terrestrial reference material SRM979 (δ53/52CrSRM979 values) - of planetary silicate reservoirs might thus yield information about the conditions of planetary metal segregation processes when compared to chondrites. The stable Cr isotopic compositions of 7 carbonaceous chondrites, 11 ordinary chondrites, 5 HED achondrites and 2 martian meteorites determined by a double spike MC-ICP-MS method are within uncertainties indistinguishable from each other and from the previously determined δ53/52CrSRM979 value of -0.124 ± 0.101‰ for the igneous silicate Earth. Extensive quality tests support the accuracy of the stable Cr isotope determinations of various meteorites and terrestrial silicates reported here. The uniformity in stable Cr isotope compositions of samples from planetary silicate mantles and undifferentiated meteorites indicates that metal-silicate differentiation of Earth, Mars and the HED parent body did not cause measurable stable Cr isotope fractionation between these two reservoirs. Our results also imply that the accretionary disc, at least in the inner solar system, was homogeneous in its stable Cr isotopic composition and that potential volatility loss of chromium during accretion of the terrestrial planets was not accompanied by measurable stable isotopic fractionation. Small but reproducible variations in δ53/52CrSRM979 values of terrestrial magmatic rocks point to natural stable Cr isotope variations within Earth's silicate reservoirs. Further and more detailed studies are required to investigate whether silicate

Sixty thousand years of magmatic volatile history before the caldera-forming eruption of Mount Mazama, Crater Lake, Oregon

Science.gov (United States)

Wright, Heather M.; Bacon, Charles R.; Vazquez, Jorge A.; Sisson, Thomas W.

2012-01-01

The well-documented eruptive history of Mount Mazama, Oregon, provides an excellent opportunity to use pre-eruptive volatile concentrations to study the growth of an explosive silicic magmatic system. Melt inclusions (MI) hosted in pyroxene and plagioclase crystals from eight dacitic–rhyodacitic eruptive deposits (71–7.7 ka) were analyzed to determine variations in volatile-element concentrations and changes in magma storage conditions leading up to and including the climactic eruption of Crater Lake caldera. Temperatures (Fe–Ti oxides) increased through the series of dacites, then decreased, and increased again through the rhyodacites (918–968 to ~950 to 845–895 °C). Oxygen fugacity began at nickel–nickel-oxide buffer (NNO) +0.8 (71 ka), dropped slightly to NNO +0.3, and then climbed to its highest value with the climactic eruption (7.7 ka) at NNO +1.1 log units. In parallel with oxidation state, maximum MI sulfur concentrations were high early in the eruptive sequence (~500 ppm), decreased (to ~200 ppm), and then increased again with the climactic eruption (~500 ppm). Maximum MI sulfur correlates with the Sr content (as a proxy for LREE, Ba, Rb, P2O5) of recharge magmas, represented by basaltic andesitic to andesitic enclaves and similar-aged lavas. These results suggest that oxidized Sr-rich recharge magmas dominated early and late in the development of the pre-climactic dacite–rhyodacite system. Dissolved H2O concentrations in MI do not, however, correlate with these changes in dominant recharge magma, instead recording vapor solubility relations in the developing shallow magma storage and conduit region. Dissolved H2O concentrations form two populations through time: the first at 3–4.6 wt% (with a few extreme values up to 6.1 wt%) and the second at ≤2.4 wt%. CO2 concentrations measured in a subset of these inclusions reach up to 240 ppm in early-erupted deposits (71 ka) and are below detection in climactic deposits (7.7 ka). Combined H2O and

Slab melting and magma formation beneath the southern Cascade arc

Science.gov (United States)

Walowski, Kristina J.; Wallace, Paul J.; Clynne, Michael A.; Rasmussen, D.J.; Weis, D.

2016-01-01

The processes that drive magma formation beneath the Cascade arc and other warm-slab subduction zones have been debated because young oceanic crust is predicted to largely dehydrate beneath the forearc during subduction. In addition, geochemical variability along strike in the Cascades has led to contrasting interpretations about the role of volatiles in magma generation. Here, we focus on the Lassen segment of the Cascade arc, where previous work has demonstrated across-arc geochemical variations related to subduction enrichment, and H-isotope data suggest that H2O in basaltic magmas is derived from the final breakdown of chlorite in the mantle portion of the slab. We use naturally glassy, olivine-hosted melt inclusions (MI) from the tephra deposits of eight primitive (MgO>7 wt%) basaltic cinder cones to quantify the pre-eruptive volatile contents of mantle-derived melts in this region. The melt inclusions have B concentrations and isotope ratios that are similar to mid-ocean ridge basalt (MORB), suggesting extensive dehydration of the downgoing plate prior to reaching sub-arc depths and little input of slab-derived B into the mantle wedge. However, correlations of volatile and trace element ratios (H2O/Ce, Cl/Nb, Sr/Nd) in the melt inclusions demonstrate that geochemical variability is the result of variable addition of a hydrous subduction component to the mantle wedge. Furthermore, correlations between subduction component tracers and radiogenic isotope ratios show that the subduction component has less radiogenic Sr and Pb than the Lassen sub-arc mantle, which can be explained by melting of subducted Gorda MORB beneath the arc. Agreement between pMELTS melting models and melt inclusion volatile, major, and trace element data suggests that hydrous slab melt addition to the mantle wedge can produce the range in primitive compositions erupted in the Lassen region. Our results provide further evidence that chlorite-derived fluids from the mantle portion of the

Magma Chamber Model of Batur Caldera, Bali, Indonesia: Compositional Variation of Two Facies, Large-Volume Dacitic Ignimbrites

Directory of Open Access Journals (Sweden)

Igan S. Sutawidjaja

2015-05-01

Full Text Available DOI:10.17014/ijog.2.2.111-124Batur is one of the finest known calderas on Earth, and is the source of at least two major ignimbrite eruptions with a combined volume of some 84 km3 and 19 km3. These ignimbrites have a similar compositions, raising the question of whether they are geneticaly related. The Batur Ignimbrite-1 (BI-1 is crystal poor, containing rhyodacitic (68 - 70wt % SiO2, white to grey pumices and partly welded and unwelded. The overlying Batur Ignimbrite-2 (BI-2 is a homogeneous grey to black dacitic pumices (64 - 66 wt % SiO2, unwelded and densely welded (40 - 60% vesicularity, crystal and lithic rich. Phase equilibria indicate that the Batur magma equilibrated at temperatures of 1100 - 1300oC with melt water contents of 3 - 6 wt%. The post-eruptive Batur magma was cooler (<1100oC and it is melt more water rich (> 6 wt % H2O. A pressure of 20 kbar is infered from mineral barometry for the Batur magma chamber. Magmatic chamber model is one in which crystals and melt separate from a convecting Batur magma by density differences, resulting in a stratified magma chamber with a homogeneous central zone, a crystal-rich accumulation zone near the walls or base, and a buoyant, melt-rich zone near the top. This is consistent with the estimated magma temperatures and densities: the pre-eruptive BI-1 magma was hoter (1300oC and more volatile rich (6 wt % H2O with density 2.25 g/cm3 than the BI-2 magma (1200oC; 4 wt % H2O in density was higher (2.50 g/cm3. Batur melt characteristics and intensive parameters are consistent with a volatile oversaturation-driven eruption. However, the higher H2O content, high viscosity and low crystal content of the BI-1 magma imply an external eruption trigger.

Air Sparging Versus Gas Saturated Water Injection for Remediation of Volatile LNAPL in the Borden Aquifer

Science.gov (United States)

Barker, J.; Nelson, L.; Doughty, C.; Thomson, N.; Lambert, J.

2009-05-01

In the shallow, rather homogeneous, unconfined Borden sand aquifer, field trials of air sparging (Tomlinson et al., 2003) and pulsed air sparging (Lambert et al., 2009) have been conducted, the latter to remediate a residual gasoline source emplaced below the water table. As well, a supersaturated (with CO2) water injection (SWI) technology, using the inVentures inFusion system, has been trialed in two phases: 1. in the uncontaminated sand aquifer to evaluate the radius of influence, extent of lateral gas movement and gas saturation below the water table, and 2. in a sheet pile cell in the Borden aquifer to evaluate the recovery of volatile hydrocarbon components (pentane and hexane) of an LNAPL emplaced below the water table (Nelson et al., 2008). The SWI injects water supersaturated with CO2. The supersaturated injected water moves laterally away from the sparge point, releasing CO2 over a wider area than does gas sparging from a single well screen. This presentation compares these two techniques in terms of their potential for remediating volatile NAPL components occurring below the water table in a rather homogeneous sand aquifer. Air sparging created a significantly greater air saturation in the vicinity of the sparge well than did the CO2 system (60 percent versus 16 percent) in the uncontaminated Borden aquifer. However, SWI pushed water, still supersaturated with CO2, up to about 2.5 m from the injection well. This would seem to provide a considerable advantage over air sparging from a point, in that gas bubbles are generated at a much larger radius from the point of injection with SWI and so should involve additional gas pathways through a residual NAPL. Overall, air sparging created a greater area of influence, defined by measurable air saturation in the aquifer, but air sparging also injected about 12 times more gas than was injected in the SWI trials. The pulsed air sparging at Borden (Lambert et al.) removed about 20 percent (4.6 kg) of gasoline

Io's theothermal (sulfur) - Lithosphere cycle inferred from sulfur solubility modeling of Pele's magma supply

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Battaglia, Steven M.; Stewart, Michael A.; Kieffer, Susan W.

2014-06-01

Surface deposits of volatile compounds such as water (Earth) or sulfur (Io) on volcanically active bodies suggest that a magmatic distillation process works to concentrate volatiles in surface reservoirs. On Earth, this is the combined hydrologic and tectonic cycle. On Io, sulfurous compounds are transferred from the interior to the surface reservoirs through a combination of a mantle-sourced magmatic system, vertical cycling of the lithosphere, and a sulfur-dominated crustal thermal system that we here call the "theothermal" system. We present a geochemical analysis of this process using previously inferred temperature and oxygen fugacity constraints of Pele's basaltic magma to determine the behavior of sulfur in the ionian magmas. Sulfate to sulfide ratios of Pele's magma are -4.084 ± 0.6 and -6.442 ± 0.7 log10 units, comparable to or lower than those of mid-ocean ridge basalts. This reflects the similarity of Io's oxidation state with Earth's depleted mantle as previously suggested by Zolotov and Fegley (Zolotov, M.Y., Fegley, B. [2000]. Geophys. Res. Lett. 27, 2789-2792). Our calculated limits of sulfur solubility in melts from Pele's patera (˜1100-1140 ppm) are also comparable to terrestrial mid-ocean ridge basalts, reflecting a compositional similarity of mantle sources. We propose that the excess sulfur obvious on Io's surface comes from two sources: (1) an insoluble sulfide liquid phase in the magma and (2) theothermal near-surface recycling.

Le gisement de sulfures à Ni-Cu-Au d'Älgliden, ceinture de Skellefte, en Suède : un gisement magmatique de Ni-Cu en zone de subduction

OpenAIRE

Coin , Kévin

2017-01-01

Most major sulfide Ni-Cu deposits originated from komatiitic or tholeiitic magmas that formed in association with mantle plumes. Their genesis involves the segregation of a immiscible sulfide liquid, reaction of the sulfide liquid with silicate melt to upgrade the sulfide in chalcophile elements, and the concentration of the sulfide liquid in economic amounts. Saturation in sulfide is commonly achieved by lowering the sulfide solubility via assimilation of siliceous wall rock or by increasing...

Rapid Crystallization of the Bishop Magma

Science.gov (United States)

Gualda, G. A.; Anderson, A. T.; Sutton, S. R.

2007-12-01

is 2 orders of magnitude smaller than the shortest durations derived from geochronology. In the current paradigm, this implies that the Bishop magma existed virtually free of crystals for 100-200 ka. Occasional recharge of the system could cause resorption of crystals. The challenge, however, is to explain how a large- volume, liquid- and volatile-rich system, was prevented from erupting for over 100 ka. The trouble is such that it puts into question the whole concept of a long-lived, liquid-rich magma body. Evidence has accumulated to show that the Bishop magma was stratified and did not convect during crystallization, the stratification was established prior to phenocryst crystallization, and crystal migration did not significantly perturb the stratification. All these are simpler to explain if liquid-rich magma only existed for a short period of time, and we estimate the time as being on the order of 1 ka. The geospeedometric timescale inferred can be reconciled with the geochronological evidence if we interpret zircon crystallization ages as reflecting episodic growth in response to waxing and waning of a mushy body, rather than continuous crystallization from liquid-rich magma in a long-lived, large-volume magma body. We speculate that only after 100-200 ka did favorable conditions emerge and allowed for the generation of a large volume of liquid-rich magma. Once such a body of magma was established, it progressed rather quickly towards eruption.

A magma ocean and the Earth's internal water budget

Science.gov (United States)

Ahrens, Thomas J.

1992-01-01

There are lines of evidence which relate bounds on the primordial water content of the Earth's mantle to a magma ocean and the accompanying Earth accretion process. We assume initially (before a magma ocean could form) that as the Earth accreted, it grew from volatile- (H2O, CO2, NH3, CH4, SO2, plus noble) gas-rich planetesimals, which accreted to form an initial 'primitive accretion core' (PAC). The PAC retained the initial complement of planetesimal gaseous components. Shock wave experiments in which both solid, and more recently, the gaseous components of materials such as serpentine and the Murchison meteorite have demonstrated that planetesimal infall velocities of less than 0.5 km/sec, induce shock pressures of less than 0.5 GPa and result in virtually complete retention of planetary gases.

Simultaneous counter-flow of chlorinated volatile organic compounds across the saturated-unsaturated interface region of an aquifer.

Science.gov (United States)

Ronen, Daniel; Lev-Wiener, Hagit; Graber, Ellen R; Dahan, Ofer; Weisbrod, Noam

2010-04-01

Concentrations of chlorinated volatile organic compounds (Cl-VOCs) at the saturated-unsaturated interface region (SUIR; depth of approximately 18m) of a sandy phreatic aquifer were measured in two monitoring wells located 25m apart. The concentrations of the Cl-VOCs obtained above and below the water table along a 413-day period are interpreted to depict variable, simultaneous and independent movement of trichlorothene, tetrachloroethene, 1,1-dichloroethene, cis-1,2-dichloroethene, 1,1,1-trichloroethane, chloroform and 1,1-dichloroethane vapors in opposite directions across the SUIR. Copyright (c) 2009 Elsevier Ltd. All rights reserved.

Recognizing subtle evidence for silicic magma derivation from petrochemically-similar arc crust: Isotopic and chemical evidence for the bimodal volcanic series of Gorely Volcanic Center, Kamchatka, Russia

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Seligman, A. N.; Bindeman, I. N.; Ellis, B. S.; Ponomareva, V.; Leonov, V.

2012-12-01

chemical compositions near the evolved ignimbrite compositions, strictly through 70-80% fractional crystallization at 1-2 kbars and NNO oxygen fugacity. The combination of light δ18O values as well as elevated 87Sr/86Sr and low 143Nd/144Nd values, in addition to the volumetric excess of silicic rocks suggest assimilation of the older and petrochemically-similar country-rocks (Karymshina volcano and/or the underlying Akhomten Massif). This research can be utilized for studies of other volcanoes at "long-term centers", underscoring the importance of using both isotopes and modeling of fractional crystallization to determine silicic magma derivation through coupled shallow crustal assimilation of similar older material and fractional crystallization.

The role of crystallization-driven exsolution on the sulfur mass balance in volcanic arc magmas

Science.gov (United States)

Su, Yanqing; Huber, Christian; Bachmann, Olivier; Zajacz, Zoltán; Wright, Heather M.; Vazquez, Jorge A.

2016-01-01

The release of large amounts of sulfur to the stratosphere during explosive eruptions affects the radiative balance in the atmosphere and consequentially impacts climate for up to several years after the event. Quantitative estimations of the processes that control the mass balance of sulfur between melt, crystals, and vapor bubbles is needed to better understand the potential sulfur yield of individual eruption events and the conditions that favor large sulfur outputs to the atmosphere. The processes that control sulfur partitioning in magmas are (1) exsolution of volatiles (dominantly H2O) during decompression (first boiling) and during isobaric crystallization (second boiling), (2) the crystallization and breakdown of sulfide or sulfate phases in the magma, and (3) the transport of sulfur-rich vapor (gas influx) from deeper unerupted regions of the magma reservoir. Vapor exsolution and the formation/breakdown of sulfur-rich phases can all be considered as closed-system processes where mass balance arguments are generally easier to constrain, whereas the contribution of sulfur by vapor transport (open system process) is more difficult to quantify. The ubiquitous “excess sulfur” problem, which refers to the much higher sulfur mass released during eruptions than what can be accounted for by amount of sulfur originally dissolved in erupted melt, as estimated from melt inclusion sulfur concentrations (the “petrologic estimate”), reflects the challenges in closing the sulfur mass balance between crystals, melt, and vapor before and during a volcanic eruption. In this work, we try to quantify the relative importance of closed- and open-system processes for silicic arc volcanoes using kinetic models of sulfur partitioning during exsolution. Our calculations show that crystallization-induced exsolution (second boiling) can generate a significant fraction of the excess sulfur observed in crystal-rich arc magmas. This result does not negate the important role of

The lunar core can be a major reservoir for volatile elements S, Se, Te and Sb.

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Steenstra, Edgar S; Lin, Yanhao; Dankers, Dian; Rai, Nachiketa; Berndt, Jasper; Matveev, Sergei; van Westrenen, Wim

2017-11-06

The Moon bears a striking compositional and isotopic resemblance to the bulk silicate Earth (BSE) for many elements, but is considered highly depleted in many volatile elements compared to BSE due to high-temperature volatile loss from Moon-forming materials in the Moon-forming giant impact and/or due to evaporative loss during subsequent magmatism on the Moon. Here, we use high-pressure metal-silicate partitioning experiments to show that the observed low concentrations of volatile elements sulfur (S), selenium (Se), tellurium (Te), and antimony (Sb) in the silicate Moon can instead reflect core-mantle equilibration in a largely to fully molten Moon. When incorporating the core as a reservoir for these elements, their bulk Moon concentrations are similar to those in the present-day bulk silicate Earth. This suggests that Moon formation was not accompanied by major loss of S, Se, Te, Sb from Moon-forming materials, consistent with recent indications from lunar carbon and S isotopic compositions of primitive lunar materials. This is in marked contrast with the losses of other volatile elements (e.g., K, Zn) during the Moon-forming event. This discrepancy may be related to distinctly different cosmochemical behavior of S, Se, Te and Sb within the proto-lunar disk, which is as of yet virtually unconstrained.

Zooming into the Paraná-Etendeka silicic volcanics, southern Brasil: a physical volcanological approach

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Gualda, G. A. R.; Gravley, D. M.; Harmon, L. J.; Tramontano, S.; Luchetti, A. C. F.; Nardy, A.

2015-12-01

Paraná-Etendeka volcanism led to the opening of the Atlantic Ocean during the early Cretaceous. Most Paraná research has focused on the regional scale geochemistry and geochronology. Complementarily, we have taken a physical volcanological approach to elucidate the styles and locations of silicic eruptions with a focus on extrusive vs. explosive varieties, and an ultimate goal to characterise the crustal magmatic conditions. Through satellite to microscopic observations we can zoom from volcanic edifice and deposit morphologies, remarkably preserved in the Mesozoic landscape, to primary microscopic textures. Lava domes appear in clusters with high relief and are surrounded by lower flat-topped terraces comprised of multiple tabular-shaped packages with conspicuous horizontal jointing. Joint thickness coincides with layering from mm-scale laminations to larger lens-shaped blobs up to 20 cm thick and more than a metre long. These layered deposits appear to be compressed and/or stretched into the finer laminations and grade up into the fatter lens-shaped blobs. In other regions, extensive plateaus dominate the landscape with flat-lying flow packages continuous over 10's of kilometres and possibly further. Rheomorphism is evident in places with sub-parallel joints that grade up into a zone of deformation where curvilinear to overturned joint patterns reflect lateral forcing in a more ductile flow regime. Microscopically the blobs and surrounding matrix are almost indistinguishable except for subtle differences in spherulite textures, zonal alteration and distribution of crystal sizes. Although our research is relatively nascent, our observations suggest eruptions may have ranged from edifice building effusive ones to more explosive ones, albeit possibly relatively low fire fountains feeding hybridised lava/pyroclastic flows. Some of these flows are extensive, tens to possibly hundreds of kilometres long, consistent with high eruption rates of hot magma. These

Helium isotope data from the Goldfield epithermal system, Nevada: Evidence for volatile input from a primitive mantle source during ore formation

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Hofstra, A. H.; Manning, A. H.

2013-12-01

Goldfield is the largest high sulfidation epithermal gold mining district in the United States with over 130 t of gold production and 23 sq. km. of argillic alteration (with alunite, pyrophyllite, or kaolinite). It formed at 20.0×0.5 Ma in an andesite to rhyolite volcanic field in the ancestral Cascades continental magmatic arc. Previous stable isotope studies of quartz, alunite, and sulfide minerals suggest that the gold ores formed in a magmatic vapor plume derived from a subjacent porphyry intrusion, which displaced and mixed with meteoric groundwater at shallow levels. The isotopic compositions of He, Ne, and Ar trapped in fluid inclusions in hydrothermal minerals (Cu-sulfides and sulfosalts, pyrite, quartz) were measured to further constrain volatile source and migration processes. Gases were released by thermal decrepitation at 300°C and analyzed using a high resolution static sector mass spectrometer. The isotopic compositions of Ne and Ar are typical of air-saturated water (ASW), indicating that the samples contain little nucleogenic Ne or radiogenic Ar derived from underlying old crustal sources. In contrast, He/Ne and He/Ar ratios are much greater than ASW, indicating that a component of He was produced in the subsurface. The wide range of He R/Ra values, 0.4 to 20, suggests that He was derived from both crustal and mantle sources. 4He/40Ar* and 4He/21Ne* systematics are characteristic of magma degassing. The highest R/Ra values (15-20) are well above those previously reported for modern volcanic rocks and geothermal fluids in subduction-related arcs. Such R/Ra values indicate a primitive mantle source, perhaps below the subducting slab. We hypothesize that the discharge of metal-laden fluids from the subjacent porphyry intrusion was influenced by the input of hot volatiles from mafic mantle-derived magmas. This scenario implies a magma column that remained open to the flux of volatiles over a considerable depth range, from the mantle to the shallow

The Origin of Silicic Arc Crust - Insights from the Northern Pacific Volcanic Arcs through Space and Time

Science.gov (United States)

Straub, S. M.; Kelemen, P. B.

2016-12-01

The remarkable compositional similarities of andesitic crust at modern convergent margins and the continental crust has long evoked the hypothesis of similar origins. Key to understanding either genesis is understanding the mode of silica enrichment. Silicic crust cannot be directly extracted from the upper mantle. Hence, in modern arcs, numerous studies - observant of the pervasive and irrefutable evidence of melt mixing - proposed that arc andesites formed by mixing of mantle-derived basaltic melts and fusible silicic material from the overlying crust. Mass balance requires the amount of silicic crust in such hybrid andesites to be on the order to tens of percent, implying that their composition to be perceptibly influenced by the various crustal basements. In order to test this hypothesis, major and trace element compositions of mafic and silicic arc magmas with arc-typical low Ce/PbMexico) were combined with Pb isotope ratios. Pb isotope ratios are considered highly sensitive to crustal contamination, and hence should reflect the variable composition of the oceanic and continental basement on which these arcs are constructed. In particular, in thick-crust continental arcs where the basement is isotopically different from the mantle and crustal assimilation thought to be most prevalent, silicic magmas must be expected to be distinct from those of the associated mafic melts. However, in a given arc, the Pb isotope ratios are constant with increasing melt silica regardless of the nature of the basement. This observation argues against a melt origin of silicic melts from the crustal basement and suggest them to be controlled by the same slab flux as their co-eval mafic counterparts. This inference is validated by the spatial and temporal pattern of arc Pb isotope ratios along the Northern Pacific margins and throughout the 50 million years of Cenozoic evolution of the Izu Bonin Mariana arc/trench system that are can be related to with systematic, `real

Depositional features and stratigraphic sections in granitic plutons: implications for the emplacement and crystallization of granitic magma

Science.gov (United States)

Wiebe, R. A.; Collins, W. J.

1998-09-01

Many granitic plutons contain sheet-like masses of dioritic to gabbroic rocks or swarms of mafic to intermediate enclaves which represent the input of higher temperature, more mafic magma during crystallization of the granitic plutons. Small-scale structures associated with these bodies (e.g. load-cast and compaction features, silicic pipes extending from granitic layers into adjacent gabbroic sheets) indicate that the sheets and enclave swarms were deposited on a floor of the magma chamber (on granitic crystal mush and beneath crystal-poor magma) while the mafic magma was incompletely crystallized. These structures indicate 'way up', typically toward the interior of the intrusions, and appear to indicate that packages of mafic sheets and enclave concentrations in these plutons are a record of sequential deposition. Hence, these plutons preserve a stratigraphic history of events involved in the construction (filling, replenishment) and crystallization of the magma chamber. The distinctive features of these depositional portions of plutons allow them to be distinguished from sheeted intrusions, which usually preserve mutual intrusive contacts and 'dike-sill' relations of different magma types. The considerable thickness of material that can be interpreted as depositional, and the evidence for replenishment, suggest that magma chamber volumes at any one time were probably much less than the final size of the pluton. Thus, magma chambers may be constructed much more slowly than presently envisaged. The present steep attitudes of these structures in many plutons may have developed gradually as the floor of the chamber (along with the underlying solidified granite and country rock) sank during continuing episodes of magma chamber replenishment. These internal magmatic structures support recent suggestions that the room problem for granites could be largely accommodated by downward movement of country rock beneath the magma chamber.

Modelling of Magma Density and Viscocity Changes and Their Influences towards the Characteristic of Kelud Volcano Eruption

Directory of Open Access Journals (Sweden)

Hanik Humaida

2014-06-01

Full Text Available DOI: 10.17014/ijog.v6i4.129The effusive eruption of Kelud Volcano in 2007 was different from the previous ones, which in general were more explosive. Among others, density and viscosity are factors that determine the type of eruption. Therefore, the study on the difference of the recent eruption style based on the density and viscosity of magma was carried out. The method used in this study was based on geochemical analysis of the rock and then a modeling was established by using the above parameter. The study on the explosive eruption was emphasized on the data of 1990 eruption, whereas the effusive eruption was based on the data of 2007 eruption. The result shows that the magma viscosity of Kelud Volcano depend on the H O concentration as one of the volatile compound in magma, and temperature which gives the exponential equation. The higher the increase of H O content the smaller the value of its viscosity as well as the higher the temperature. The H O content in silica fluid can break the polymer bond of the silica fluid, because a shorter polymer will produce a lower viscosity. The density of the silica content of Kelud Volcano ranges between andesitic and basaltic types, but andesite is more likely. The fluid density of the material of 1990 eruption is different from 2007 eruption. Compared to the 2007, the 1990 eruption material gave a lower density value in its silica fluid than that of the 2007 one. The low density value of the silica fluid of the 1990 eruption material was reflecting a more acid magma. The level of density value of silica fluid depends on its temperature. At the temperature of 1073 K the density of the 1990 Kelud magma is 2810 kg/m3 and the 2007 magma is 2818 kg/m3, whereas at a temperature of 1673 K, the density is 2672 kg/m3 and 2682 kg/m3 of the 1990 and 2007 eruptions respectively. A modeling by using an ideal gas law of Henry’s Law illustrated that the ascent of Kelud’s magma to the surface may cause changes

Terrestrial magma ocean and core segregation in the earth

Science.gov (United States)

Ohtani, Eiji; Yurimoto, Naoyoshi

1992-01-01

According to the recent theories of formation of the earth, the outer layer of the proto-earth was molten and the terrestrial magma ocean was formed when its radius exceeded 3000 km. Core formation should have started in this magma ocean stage, since segregation of metallic iron occurs effectively by melting of the proto-earth. Therefore, interactions between magma, mantle minerals, and metallic iron in the magma ocean stage controlled the geochemistry of the mantle and core. We have studied the partitioning behaviors of elements into the silicate melt, high pressure minerals, and metallic iron under the deep upper mantle and lower mantle conditions. We employed the multi-anvil apparatus for preparing the equilibrating samples in the ranges from 16 to 27 GPa and 1700-2400 C. Both the electron probe microanalyzer (EPMA) and the Secondary Ion Mass spectrometer (SIMS) were used for analyzing the run products. We obtained the partition coefficients of various trace elements between majorite, Mg-perovskite, and liquid, and magnesiowustite, Mg-perovskite, and metallic iron. The examples of the partition coefficients of some key elements are summarized in figures, together with the previous data. We may be able to assess the origin of the mantle abundances of the elements such as transition metals by using the partitioning data obtained above. The mantle abundances of some transition metals expected by the core-mantle equilibrium under the lower mantle conditions cannot explain the observed abundance of some elements such as Mn and Ge in the mantle. Estimations of the densities of the ultrabasic magma Mg-perovskite at high pressure suggest existence of a density crossover in the deep lower mantle; flotation of Mg-perovskite occurs in the deep magma ocean under the lower mantle conditions. The observed depletion of some transition metals such as V, Cr, Mn, Fe, Co, and Ni in the mantle may be explained by the two stage process, the core-mantle equilibrium under the lower

Reassessment of the origin of the Dun Mountain Ophiolite, New Zealand : Nd-isotopic and geochemical evolution of magma suites

International Nuclear Information System (INIS)

Sivell, W.J.; McCulloch, M.T.

2000-01-01

Magmatic suites with contrasting isotopic and geochemical compositions, sequentially emplaced in different tectonic regimes, comprise the Dun Mountain Ophiolite Belt (DMOB), New Zealand. At D'Urville Island, the northernmost exposure of the DMOB, earliest erupted (stage 1) pillow basalts ε Nd (T) = +6.3 to +7.5, and are incompatible element enriched, like basalts from geochemically anomalous ridge segments. Overlying stage 2 basalts (sheeted flows) show a narrow range of ε Nd (T) = +8.3 + or -0.2, with chemical characteristics of depleted backarc basin basalts. These rocks are intruded by mafic to silicic stage 3 magmas, which have high uniform initial 143 Nd/ 144 Nd ratios (ε Nd (T) = +9.3 + or -0.2) over a wide range of 147 Sm/ 144 Nd values (yielding a precise Early Permian Nd-isotope age of 278 ± 4 Ma (MSWD = 0.48)). Stage 3 magmas show pronounced subduction-related geochemical signatures similar to island arc tholeiites (IAT) from immature arcs. They are closely analogous to some (boninite)-IAT magmas which characterise 'infant arc' eruptive activity in forearc basins of present-day Western Pacific island arc systems. A wide variety of stage 3 magma compositions, ranging from near-primary basaltic dikes (Mg = 74) to extremely fractionated silicic plagiogranites with uniformly very depleted isotopic ratios, is consistent with slow spreading rates which gave rise to polybaric, closed-system fractionation of magmas and periodic chamber abandonment. Some stage 3 rocks with SiO 2 levels in the andesite range have low-TiO 2 contents and high Mg, and may be fractionated equivalents of boninites. High ε Nd (T) values of stage 3 magmas indicate a lack of subducted sediment with inherited crustal residence signatures, and reflect the extent of supra-subduction zone (SSZ) mantle wedge depletion. DMOB stage 3 magmas may represent foreac magmatism that was the precursor to normal subduction-related volcanism established by c. 265 Ma in the Brook Street Arc and derived

Magnetic mineralogy and rock magnetic properties of silicate and carbonatite rocks from Oldoinyo Lengai volcano (Tanzania)

Science.gov (United States)

Mattsson, H. B.; Balashova, A.; Almqvist, B. S. G.; Bosshard-Stadlin, S. A.; Weidendorfer, D.

2018-06-01

Oldoinyo Lengai, a stratovolcano in northern Tanzania, is most famous for being the only currently active carbonatite volcano on Earth. The bulk of the volcanic edifice is dominated by eruptive products produced by silica-undersaturated, peralkaline, silicate magmas (effusive, explosive and/or as cumulates at depth). The recent (2007-2008) explosive eruption produced the first ever recorded pyroclastic flows at this volcano and the accidental lithics incorporated into the pyroclastic flows represent a broad variety of different rock types, comprising both extrusive and intrusive varieties, in addition to various types of cumulates. This mix of different accidental lithics provides a unique insight into the inner workings of the world's only active carbonatite volcano. Here, we focus on the magnetic mineralogy and the rock magnetic properties of a wide selection of samples spanning the spectrum of Oldoinyo Lengai rock types compositionally, as well from a textural point of view. Here we show that the magnetic properties of most extrusive silicate rocks are dominated by magnetite-ulvöspinel solid solutions, and that pyrrhotite plays a larger role in the magnetic properties of the intrusive silicate rocks. The natrocarbonatitic lavas, for which the volcano is best known for, show distinctly different magnetic properties in comparison with the silicate rocks. This discrepancy may be explained by abundant alabandite crystals/blebs in the groundmass of the natrocarbonatitic lavas. A detailed combination of petrological/mineralogical studies with geophysical investigations is an absolute necessity in order to understand, and to better constrain, the overall architecture and inner workings of the subvolcanic plumbing system. The results presented here may also have implications for the quest in order to explain the genesis of the uniquely natrocarbonatitic magmas characteristic of Oldoinyo Lengai.

Core-Mantle Partitioning of Volatile Elements and the Origin of Volatile Elements in Earth and Moon

Science.gov (United States)

Righter, K.; Pando, K.; Danielson, L.; Nickodem, K.

2014-01-01

Depletions of siderophile elements in mantles have placed constraints on the conditions on core segregation and differentiation in bodies such as Earth, Earth's Moon, Mars, and asteroid 4 Vesta. Among the siderophile elements there are a sub-set that are also volatile (volatile siderophile elements or VSE; Ga, Ge, In, As, Sb, Sn, Bi, Zn, Cu, Cd), and thus can help to constrain the origin of volatile elements in these bodies, and in particular the Earth and Moon. One of the fundamental observations of the geochemistry of the Moon is the overall depletion of volatile elements relative to the Earth, but a satisfactory explanation has remained elusive. Hypotheses for Earth include addition during accretion and core formation and mobilized into the metallic core, multiple stage origin, or addition after the core formed. Any explanation for volatile elements in the Earth's mantle must also be linked to an explanation of these elements in the lunar mantle. New metal-silicate partitioning data will be applied to the origin of volatile elements in both the Earth and Moon, and will evaluate theories for exogenous versus endogenous origin of volatile elements.

Upward migration of Vesuvius magma chamber over the past 20,000 years.

Science.gov (United States)

Scaillet, B; Pichavant, M; Cioni, R

2008-09-11

Forecasting future eruptions of Vesuvius is an important challenge for volcanologists, as its reawakening could threaten the lives of 700,000 people living near the volcano. Critical to the evaluation of hazards associated with the next eruption is the estimation of the depth of the magma reservoir, one of the main parameters controlling magma properties and eruptive style. Petrological studies have indicated that during past activity, magma chambers were at depths between 3 and 16 km (refs 3-7). Geophysical surveys have imaged some levels of seismic attenuation, the shallowest of which lies at 8-9 km depth, and these have been tentatively interpreted as levels of preferential magma accumulation. By using experimental phase equilibria, carried out on material from four main explosive events at Vesuvius, we show here that the reservoirs that fed the eruptive activity migrated from 7-8 km to 3-4 km depth between the ad 79 (Pompeii) and ad 472 (Pollena) events. If data from the Pomici di Base event 18.5 kyr ago and the 1944 Vesuvius eruption are included, the total upward migration of the reservoir amounts to 9-11 km. The change of preferential magma ponding levels in the upper crust can be attributed to differences in the volatile content and buoyancy of ascending magmas, as well as to changes in local stress field following either caldera formation or volcano spreading. Reservoir migration, and the possible influence on feeding rates, should be integrated into the parameters used for defining expected eruptive scenarios at Vesuvius.

Empirical constraints on partitioning of platinum group elements between Cr-spinel and primitive terrestrial magmas

Science.gov (United States)

Park, Jung-Woo; Kamenetsky, Vadim; Campbell, Ian; Park, Gyuseung; Hanski, Eero; Pushkarev, Evgeny

2017-11-01

Recent experimental studies and in situ LA-ICP-MS analysis on natural Cr-spinel have shown that Rh and IPGEs (Ir-group platinum group elements: Ru, Ir, Os) are enriched in the lattice of Cr-spinel. However, the factors controlling the partitioning behaviour of these elements are not well constrained. In this study, we report the Rh, IPGE, and trace element contents in primitive Cr-spinel, measured by LA-ICP-MS, from nine volcanic suites covering various tectonic settings including island arc picrites, boninites, large igneous province picrites and mid-ocean ridge basalts. The aim is to understand the factors controlling the enrichment of Rh and IPGEs in Cr-spinels, to estimate empirical partition coefficients between Cr-spinel and silicate melts, and to investigate the role of Cr-spinel fractional crystallization on the PGE geochemistry of primitive magmas during the early stages of fractional crystallization. There are systematic differences in trace elements, Rh and IPGEs in Cr-spinels from arc-related magmas (Arc Group Cr-spinel), intraplate magmas (Intraplate Group Cr-spinel), and mid-ocean ridge magmas (MORB Group Cr-spinel). Arc Group Cr-spinels are systematically enriched in Sc, Co and Mn and depleted in Ni compared to the MORB Group Cr-spinels. Intraplate Group Cr-spinels are distinguished from the Arc Group Cr-spinels by their high Ni contents. Both the Arc and Intraplate Group Cr-spinels have total Rh and IPGE contents of 22-689 ppb whereas the MORB Group Cr-spinels are depleted in Rh and IPGE (total time-resolved spectra of LA-ICP-MS data for Cr-spinels mostly show constant count rates for trace element and Rh and IPGEs, suggesting homogeneous distribution of these elements in Cr-spinels. The PGE spikes observed in several Cr-spinels were interpreted to be PGE-bearing mineral inclusions and excluded from calculating the PGE contents of the Cr-spinels. On primitive mantle normalized diagrams the Arc Group Cr-spinels are characterized by a fractionated

Constraints on the source of Cu in a submarine magmatic-hydrothermal system, Brothers volcano, Kermadec island arc

Science.gov (United States)

Keith, Manuel; Haase, Karsten M.; Klemd, Reiner; Smith, Daniel J.; Schwarz-Schampera, Ulrich; Bach, Wolfgang

2018-05-01

Most magmatic-hydrothermal Cu deposits are genetically linked to arc magmas. However, most continental or oceanic arc magmas are barren, and hence new methods have to be developed to distinguish between barren and mineralised arc systems. Source composition, melting conditions, the timing of S saturation and an initial chalcophile element-enrichment represent important parameters that control the potential of a subduction setting to host an economically valuable deposit. Brothers volcano in the Kermadec island arc is one of the best-studied examples of arc-related submarine magmatic-hydrothermal activity. This study, for the first time, compares the chemical and mineralogical composition of the Brothers seafloor massive sulphides and the associated dacitic to rhyolitic lavas that host the hydrothermal system. Incompatible trace element ratios, such as La/Sm and Ce/Pb, indicate that the basaltic melts from L'Esperance volcano may represent a parental analogue to the more evolved Brothers lavas. Copper-rich magmatic sulphides (Cu > 2 wt%) identified in fresh volcanic glass and phenocryst phases, such as clinopyroxene, plagioclase and Fe-Ti oxide suggest that the surrounding lavas that host the Brothers hydrothermal system represent a potential Cu source for the sulphide ores at the seafloor. Thermodynamic calculations reveal that the Brothers melts reached volatile saturation during their evolution. Melt inclusion data and the occurrence of sulphides along vesicle margins indicate that an exsolving volatile phase extracted Cu from the silicate melt and probably contributed it to the overlying hydrothermal system. Hence, the formation of the Cu-rich seafloor massive sulphides (up to 35.6 wt%) is probably due to the contribution of Cu from a bimodal source including wall rock leaching and magmatic degassing, in a mineralisation style that is hybrid between Cyprus-type volcanic-hosted massive sulphide and subaerial epithermal-porphyry deposits.

The Life and Times of Supervolcanoes: Inferences from Long Valley Caldera

Science.gov (United States)

Simon, Justin

2014-01-01

Cataclysmic eruptions of silicic magma from "supervolcanoes" are among the most awe-inspiring natural phenomena found in the geologic record, in terms of size, power, and potential hazard. Based on the repose intervals between eruptions of this magnitude, the magmas responsible for them could accumulate gradually in the shallow crust over time scales that may be in excess of a million years (Smith, 1979; Spera and Crisp, 1981; Shaw, 1985). Pre-eruption magma residence time scales can also be inferred from the age difference between eruption (i.e., using 40Ar/39Ar dating to determine the time when hot erupted material cools to below its Ar closure temperature, 200 to 600 degC) and early pre-eruption crystallization (i.e., zircon saturation temperatures; Reid et al., 1997). I will discuss observations from Long Valley a Quaternary volcanic center in California. Long Valley is a voluminous, dominantly silicic caldera system. Based on extensive dating of accessory minerals (e.g., U-Th-Pb dating of zircon and allanite) along with geochemical and isotopic data we find that silicic magmas begin to crystallize 10's to 100's of thousands of years prior to their eruption and that rhyolites record episodes of punctuated and independent evolution rather than the periodic tapping of a long-lived magma. The more punctuated versus more gradual magma accumulation rates required by the absolute and model ages, respectively, imply important differences in the mass and heat fluxes associated with the generation, differentiation, and storage of voluminous rhyolites and emphasize the need to reconcile the magmatic age differences.

Magmatic Volatiles as an Amplifier of Centrifugal Volcanism

Science.gov (United States)

Pratt, V. R.

2017-12-01

There is a striking correlation between negated Length of Day -LOD and the 60-70 year period in 20th century global climate, associated by some with the so-called Atlantic Multidecadal Oscillation or AMO. A number of authors have suggested mechanisms by which the former might cause the latter. One such that this author finds quite compelling is that gravity fluctuations at low latitudes increase essentially linearly with LOD fluctuations and therefore moves magma towards or away from the surface as LOD decreases or increases, i.e. angular velocity increases or decreases, respectively. At AGU FM2016 we proposed the term "centrifugal volcanism" for this mechanism and listed four possible objections to it, explaining three to our satisfaction. The remaining objection is the very obvious one that the 4 ms increase in LOD between 1880 and 1910 seems far too small to be able to account for the observed variation of about a quarter of a degree. A basic mechanism underlying many violent eruptions is the strong positive feedback between reduction of pressure in magma and evaporation of dissolved volatiles found in some magmas, driving the magma outwards and thereby further reducing the pressure. The normal state of magma is equilibrium. Any fluctuation in gravity, even a very small one, can be sufficient to shift this equilibrium sufficiently far to set this positive feedback in motion. The relevant electrical analogy would be an operational amplifier whose amplification is greatly increased by a positive feedback. We therefore propose that the same mechanism responsible for some violent eruptions also serves to amplify the tiny changes in gravity sufficiently to increase or decrease the vertical component of the movement of magma in general. This movement, felt throughout the planet albeit most strongly at low latitudes, influences the temperature at ocean bottoms wherever there is a significant level of magmatic volatiles. This in turn creates thermals that are large

Can Fractional Crystallization of a Lunar Magma Ocean Produce the Lunar Crust?

Science.gov (United States)

Rapp, Jennifer F.; Draper, David S.

2013-01-01

New techniques enable the study of Apollo samples and lunar meteorites in unprecedented detail, and recent orbital spectral data reveal more about the lunar farside than ever before, raising new questions about the supposed simplicity of lunar geology. Nevertheless, crystallization of a global-scale magma ocean remains the best model to account for known lunar lithologies. Crystallization of a lunar magma ocean (LMO) is modeled to proceed by two end-member processes - fractional crystallization from (mostly) the bottom up, or initial equilibrium crystallization as the magma is vigorously convecting and crystals remain entrained, followed by crystal settling and a final period of fractional crystallization [1]. Physical models of magma viscosity and convection at this scale suggest that both processes are possible. We have been carrying out high-fidelity experimental simulations of LMO crystallization using two bulk compositions that can be regarded as end-members in the likely relevant range: Taylor Whole Moon (TWM) [2] and Lunar Primitive Upper Mantle (LPUM) [3]. TWM is enriched in refractory elements by 1.5 times relative to Earth, whereas LPUM is similar to the terrestrial primitive upper mantle, with adjustments made for the depletion of volatile alkalis observed on the Moon. Here we extend our earlier equilibrium-crystallization experiments [4] with runs simulating full fractional crystallization

Insight into silicate-glass corrosion mechanisms

Energy Technology Data Exchange (ETDEWEB)

Cailleteau, C; Angeli, F; Gin, S; Jollivet, P [CEA VALRHO, DEN, Lab Etude Comportement Long Terme, F-30207 Bagnols Sur Ceze, (France); Devreux, F [Ecole Polytech, CNRS, Lab Phys Mat Condensee, F-91128 Palaiseau, (France); Jestin, J [CEA, CNRS, Lab Leon Brillouin, F-91191 Gif Sur Yvette, (France); Spalla, O [CEA, DSM, Lab Interdisciplinaire Org Nanometr et Supramol, F-91191 Gif Sur Yvette, (France)

2008-07-01

The remarkable chemical durability of silicate glass makes it suitable for a wide range of applications. The slowdown of the aqueous glass corrosion kinetics that is frequently observed at long time is generally attributed to chemical affinity effects (saturation of the solution with respect to silica). Here, we demonstrate a new mechanism and highlight the impact of morphological transformations in the alteration layer on the leaching kinetics. A direct correlation between structure and reactivity is revealed by coupling the results of several structure-sensitive experiments with numerical simulations at mesoscopic scale. The sharp drop in the corrosion rate is shown to arise from densification of the outer layers of the alteration film, leading to pore closure. The presence of insoluble elements in the glass can inhibit the film restructuring responsible for this effect. This mechanism may be more broadly applicable to silicate minerals. (authors)

Temperature evolution during magma ascent in basaltic effusive eruptions: A numerical application to Stromboli volcano

Science.gov (United States)

La Spina, G.; Burton, M.; de'Michieli Vitturi, M.

2015-09-01

The dynamics of magma ascent are controlled by the complex, interdependent processes of crystallisation, rheological evolution, gas exsolution, outgassing, non-ideal gas expansion and temperature evolution. Temperature changes within the conduit, in particular, play a key role on ascent dynamics, since temperature strongly controls the crystallisation process, which in turn has an impact on viscosity and thus on magma ascent rate. The cooling produced by gas expansion is opposed by the heat produced by crystallisation, and therefore the temperature profile within the conduit is quite complex. This complexity means that unravelling the dynamics controlling magma ascent requires a numerical model. Unfortunately, comprehensive, integrated models with full thermodynamic treatment of multiple phases and rheological evolution are challenging to produce, due to the numerical challenges involved. Until now, models have tended to focus on aspects of the problem, without a holistic approach in which petrological, thermodynamic, rheological and degassing processes, and their interactions, were all explicitly addressed and quantified. Here, we present a new, multiphase steady-state model for magma ascent in which the main physical and chemical processes, such as crystallisation, degassing, outgassing, rheological evolution and temperature variations, are quantitatively calculated. Basaltic magma's crystallisation and flow are sensitive to initial temperature and volatile content, and therefore we investigate temperature variations during magma ascent in a basaltic system with a range of volatile contents. As a test case, we use one of the most well-studied recent basaltic effusive eruptions: the 2007 eruption of Stromboli, Italy. Assuming equilibrium crystallisation and exsolution, we compare the solutions obtained both with and without an isothermal constraint, finding that temperature variations within the conduit have a significant influence on the ascent dynamics and

Ultra-high chlorine in submarine Kı̄lauea glasses: Evidence for direct assimilation of brine by magma

Science.gov (United States)

Coombs, Michelle L.; Sisson, Thomas W.; Kimura, Jun-Ichi

2004-01-01

Basaltic glass grains from the submarine south flank of Kı̄lauea, Hawai′i, have Cl concentrations of 0.01–1.68 wt%, the latter being the highest Cl content yet recorded for a Hawaiian glass. The high-Cl glass grains are products of brine assimilation by tholeiite magma. The glasses are grains in a sandstone clast from bedded breccias draping the southwestern margin of Kı̄lauea’s submarine midslope bench. The clast contains two distinct suites of glass grains: abundant degassed tholeiites, perhaps derived from subaerial lavas of Mauna Loa that shattered upon ocean entry, and a smaller population of Kea-type tholeiite (n=17 analyzed) that erupted subaqueously, based on elevated S (780–1050 ppm), H2O (0.42–1.27 wt%), and CO2 (1000 ppm, six >5000 ppm, and two grains have >10 000 ppm dissolved Cl. Abundances of H2O, Na2O, K2O, and several trace elements increase regularly with Cl concentration, and we estimate that Cl enrichment was due to up to 13 wt% addition of a brine consisting of 78% H2O (wt), 13% Cl, 4.4% Na, 2.6% K, 2.6% Ca, 620 ppm Ba, 360 ppm Sr, 65 ppm Rb, and 7 ppm Pb. The large amounts of brine addition argue against bulk assimilation of low-porosity brine-bearing rock. The brine’s composition is appropriate for a seawater-derived hydrothermal fluid that reacted with basaltic wall rocks at T>100°C, losing Mg and S and gaining K, Ca, Rb, Ba, Sr, and Pb, followed by phase separation near 500°C and ∼50 MPa (5 km below sea level at hydrostatic pressure). Brine was assimilated at or near the depth it formed, as estimated on petrologic grounds, but under lithostatic conditions. The highest extents of assimilation either forced volatile saturation of the magma or enriched already coexisting magmatic vapor in H2O. Possible mechanisms for assimilation are: (1) forcible injection of brine into magma during bursting of overpressured pockets heated by new dikes, or (2) intrusion of magma into lenses or sills occupied by trapped brine.

Magma Chambers, Thermal Energy, and the Unsuccessful Search for a Magma Chamber Thermostat

Science.gov (United States)

Glazner, A. F.

2015-12-01

Although the traditional concept that plutons are the frozen corpses of huge, highly liquid magma chambers ("big red blobs") is losing favor, the related notion that magma bodies can spend long periods of time (~106years) in a mushy, highly crystalline state is widely accepted. However, analysis of the thermal balance of magmatic systems indicates that it is difficult to maintain a significant portion in a simmering, mushy state, whether or not the system is eutectic-like. Magma bodies cool primarily by loss of heat to the Earth's surface. The balance between cooling via energy loss to the surface and heating via magma accretion can be denoted as M = ρLa/q, where ρ is magma density, L is latent heat of crystallization, a is the vertical rate of magma accretion, and q is surface heat flux. If M>1, then magma accretion outpaces cooling and a magma chamber forms. For reasonable values of ρ, L, and q, the rate of accretion amust be > ~15 mm/yr to form a persistent volume above the solidus. This rate is extremely high, an order of magnitude faster than estimated pluton-filling rates, and would produce a body 10 km thick in 700 ka, an order of magnitude faster than geochronology indicates. Regardless of the rate of magma supply, the proportion of crystals in the system must vary dramatically with depth at any given time owing to transfer of heat. Mechanical stirring (e.g., by convection) could serve to homogenize crystal content in a magma body, but this is unachievable in crystal-rich, locked-up magma. Without convection the lower part of the magma body becomes much hotter than the top—a process familiar to anyone who has scorched a pot of oatmeal. Thermal models that succeed in producing persistent, large bodies of magma rely on scenarios that are unrealistic (e.g., omitting heat loss to the planet's surface), self-fulfilling prophecies (e.g., setting unnaturally high temperatures as fixed boundary conditions), or physically unreasonable (e.g., magma is intruded

Volcanic-plutonic connections and metal fertility of highly evolved magma systems: A case study from the Herberton Sn-W-Mo Mineral Field, Queensland, Australia

Science.gov (United States)

Cheng, Yanbo; Spandler, Carl; Chang, Zhaoshan; Clarke, Gavin

2018-03-01

Understanding the connection between the highly evolved intrusive and extrusive systems is essential to explore the evolution of high silicic magma systems, which plays an important role in discussions of planetary differentiation, the growth of continents, crustal evolution, and the formation of highly evolved magma associated Sn-W-Mo mineral systems. To discern differences between "fertile" and "non-fertile" igneous rocks associated with Sn-W-Mo mineralization and reveal the genetic links between coeval intrusive and extrusive rocks, we integrate whole rock geochemistry, geochronology and Hf isotope signatures of igneous zircons from contemporaneous plutonic and volcanic rocks from the world-class Herberton Mineral Field of Queensland, Australia. The 310-300 Ma intrusive rocks and associated intra-plutonic W-Mo mineralization formed from relatively oxidized magmas after moderate degrees of crystal fractionation. The geochemical and isotopic features of the coeval volcanic succession are best reconciled utilizing the widely-accepted volcanic-plutonic connection model, whereby the volcanic rocks represent fractionated derivatives of the intrusive rocks. Older intrusions emplaced at 335-315 Ma formed from relatively low fO2 magmas that fractionated extensively to produce highly evolved granites that host Sn mineralization. Coeval volcanic rocks of this suite are compositionally less evolved than the intrusive rocks, thereby requiring a different model to link these plutonic-volcanic sequences. In this case, we propose that the most fractionated magmas were not lost to volcanism, but instead were effectively retained at the plutonic level, which allowed further localized build-up of volatiles and lithophile metals in the plutonic environment. This disconnection to the volcanism and degassing may be a crucial step for forming granite-hosted Sn mineralization. The transition between these two igneous regimes in Herberton region over a ∼30 m.y. period is attributed to

The role of silicate surfaces on calcite precipitation kinetics

DEFF Research Database (Denmark)

Stockmann, Gabrielle J.; Wolff-Boenisch, Domenik; Bovet, Nicolas Emile

2014-01-01

The aim of this study is to illuminate how calcite precipitation depends on the identity and structure of the growth substrate. Calcite was precipitated at 25°C from supersaturated aqueous solutions in the presence of seeds of either calcite or one of six silicate materials: augite, enstatite......, labradorite, olivine, basaltic glass and peridotite rock. Calcite saturation was achieved by mixing a CaCl2-rich aqueous solution with a NaHCO3-Na2CO3 aqueous buffer in mixed-flow reactors containing 0.5-2g of mineral, rock, or glass seeds. This led to an inlet fluid calcite saturation index of 0.6 and a p...

Zoning and exsolution in cumulate alkali feldspars from the eruption (12.9 Ka) of Laacher see volcano (Western Germany) as an indicator of time-scales and dynamics of carbonate-silicate unmixing

Science.gov (United States)

Sourav Rout, Smruti; Wörner, Gerhard

2017-04-01

Time-scales extracted from the detailed analysis of chemically zoned minerals provide insights into crystal ages, magma storage and compositional evolution, including mixing and unmixing events. This allows having a better understanding of pre-eruptive history of large and potentially dangerous magma chambers. We present a comprehensive study of chemical diffusion across zoning and exsolution patterns of alkali feldspars in carbonatite-bearing cognate syenites from the 6.3 km3 (D.R.E) phonolitic Laacher See Tephra (LST) eruption 12.9 ka ago. The Laacher See volcano is located in the Quaternary East Eifel volcanic field of the Paleozoic Rhenish Massif in Western Germany and has produced a compositionally variable sequence in a single eruption from a magma chamber that was zoned from mafic phonolite at the base to highly evolved, actively degassing phonolite magma at the top. Diffusion chronometry is applied to major and trace element compositions obtained on alkali feldspars from carbonate-bearing syenitic cumulates. Methods used were laser ablation inductively coupled plasma mass spectrometry (LA ICP-MS) in combination with energy-dispersive and wavelength-dispersive electron microprobe analyses (EDS & WDS-EMPA). The grey scale values extracted from multiple accumulations of back-scattered electron images represent the K/Na ratio owing to the extremely low concentrations of Ba and Sr (transition and phase separation). A distinctive uphill diffusive analysis is used specifically for the phase separation in the case of exsolution features (comprising of albite- and orthoclase-rich phases) in sanidines. The error values are aggregates of propagated error through calculations and the uncertainty in temperature values. Trace element compositional data of distinct feldspar compositions that are assumed to have grown before and after silicate-carbonate unmixing are used to estimate partition coefficients between carbonate and silicate melt. The resulting values correlate

Quantitative evaluation of the effect of H2O degassing on the oxidation state of magmas

Science.gov (United States)

Lange, R. A.; Waters, L.

2014-12-01

The extent to which degassing of the H2O component affects the oxidation state of hydrous magmas is widely debated. Several researchers have examined how degassing of mixed H-C-O-S-Cl fluids may change the Fe3+/FeT ratio of various magmas, whereas our focus is on the H2O component. There are two ways that degassing of H2O by itself may cause oxidation: (1) the reaction: H2O (melt) + 2FeO (melt) = H2 (fluid) + Fe2O3 (melt), and/or (2) if dissolved water preferentially enhances the activity of ferrous vs. ferric iron in magmatic liquids. In this study, a comparison is made between the pre-eruptive oxidation states of 14 crystal-poor, jet-black obsidian samples (obtained from two Fe-Ti oxides) and their post-eruptive values (analyzed with the Wilson 1960 titration method tested against USGS standards). The obsidians are from Medicine Lake (CA), Long Valley (CA), and the western Mexican arc; all have low FeOT (1.1-2.1 wt%), rendering their Fe2+/Fe3+ ratios highly sensitive to the possible effects of substantial H2O degassing. The Fe-Ti oxide thermometer/oxybarometer of Ghiorso and Evans, (2008) gave temperatures for the 14 samples that range for 720 to 940°C and ΔNNO values of -0.9 to +1.4. With temperature known, the plagioclase-liquid hygrometer was applied and show that ≤ 6.5 wt% H2O was dissolved in the melts prior to eruption. In addition, pre-eruptive Cl and S concentrations were constrained on the basis of apatite analyses (Webster et al., 2009) and sulfur concentrations needed for saturation with pyrrhotite (Clemente et al., 2004), respectively. Maximum pre-eruptive chlorine and sulfur contents are 6000 and 200 ppm, respectively. After eruption, the rhyolites lost nearly all of their volatiles. Our results indicate no detectable change between pre- and post-eruptive Fe2+ concentrations, with an average deviation of ± 0.1 wt % FeO. Although degassing of large concentrations of S and/or Cl may affect the oxidation state of magmas, at the pre-eruptive levels

Silicate liquid immiscibility in magmas and in the system K2O-FeO-AI2O3-SiO2: an example of serendipity

Science.gov (United States)

Roedder, E.

1978-01-01

system, compositions near it show a number of phase changes and large amounts of crystallization with small temperature changes, generally in the range 1100-1150 C. Similar low-temperature, high-alkali immiscibility was discovered in a few exploratory runs in the equivalent systems with Rb or Cs substituting for K. But not in those with Li or Na. A review of the compositions and general behavior of systems involving immiscibility, both stable and metastable, and of the evidence for natural immiscibility. indicates that it may be a much more common feature than generally thought. Several examples of natural immiscibility are detailed; most yield a felsic. alkali-aluminosilicate melt and a mafic melt. from a wide variety of generally basaltic parental magmas, both under- and over saturated. Unfortunately, the best line of evidence for immiscibility in terrestrial rocks, a sharply defined meniscus between two compositionally disparate glasses, is by its very nature self-destructing, since it is effectively eliminated by either crystallization or gravitative separation and coalescence into separate magmas. Verification of operation of the exosolutionor 'splitting' process on a large scale will probably require careful study of isotopic and trace element partitioning in both laboratory and field. ?? 1978.

Petrogenesis of early cretaceous silicic volcanism in SE Uruguay. The role of mantle and crustal sources

International Nuclear Information System (INIS)

Lustrino, Michele; Morbidelli, Lucio; Marrazzo, Marianna; Melluso, Leone; Brotzu, Pietro; Tassinari, Colombo C.G.; Gomes, Celso B.; Ruberti, Excelso

2010-01-01

Early Cretaceous (∼129 Ma) silicic rocks crop out in SE Uruguay between the Laguna Merin and Santa Lucia basins in the Lascano, Sierra Sao Miguel, Salamanca and Minas areas. They are mostly rhyolites with minor quartz-trachytes and are nearly contemporaneous with the Parana-Etendeka igneous province and with the first stages of South Atlantic Ocean opening. A strong geochemical variability (particularly evident from Rb/Nb, Nb/Y trace element ratios) and a wide range of Sr-Nd isotopic ratios ( 143 Nd/ 144 Nd (129) =0.51178-0.51209; 87 Sr/ 86 Sr (129) =0.70840-0.72417) characterize these rocks. Geochemistry allows to distinguish two compositional groups, corresponding to the north-eastern (Lascano and Sierra Sao Miguel, emplaced on the Neo-Proterozoic southern sector of the Dom Feliciano mobile belt) and south-eastern localities (Salamanca, Minas, emplaced on the much older (Archean) Nico Perez terrane or on the boundary between the Dom Feliciano and Nico Perez terranes). These compositional differences between the two groups are explained by variable mantle source and crust contributions. The origin of the silicic magmas is best explained by complex processes involving assimilation and fractional crystallization and mixing of a basaltic magma with upper crustal lithologies, for Lascano and Sierra Sao Miguel rhyolites. In the Salamanca and Minas rocks genesis, a stronger contribution from lower crust is indicated. (author)

Experimental Study of Lunar and SNC Magmas

Science.gov (United States)

Rutherford, Malcolm J.

1998-01-01

The research described in this progress report involved the study of petrological, geochemical and volcanic processes that occur on the Moon and the SNC parent body, generally accepted to be Mars. The link between these studies is that they focus on two terrestrial-type parent bodies somewhat smaller than earth, and the fact that they focus on the role of volatiles in magmatic processes and on processes of magma evolution on these planets. The work on the lunar volcanic glasses has resulted in some exciting new discoveries over the years of this grant. We discovered small metal blebs initially in the Al5 green glass, and determined the significant importance of this metal in fixing the oxidation state of the parent magma (Fogel and Rutherford, 1995). More recently, we discovered a variety of metal blebs in the Al7 orange glass. Some of these Fe-Ni metal blebs were in the glass; others were in olivine phenocrysts. The importance of these metal spheres is that they fix the oxidation state of the parent magma during the eruption, and also indicate changes during the eruption (Weitz et al., 1997) They also yield important information about the composition of the gas phase present, the gas which drove the lunar fire-fountaining. One of the more exciting and controversial findings in our research over the past year has been the possible fractionation of H from D during shock (experimental) of hornblende bearing samples (Minitti et al., 1997). This research is directed at explaining some of the low H2O and high D/H observed in hydrous phases in the SNC meteorites.

Dynamics of differentiation in magma reservoirs

Science.gov (United States)

Jaupart, Claude; Tait, Stephen

1995-09-01

In large magma chambers, gradients of temperature and composition develop due to cooling and to fractional crystallization. Unstable density differences lead to differential motions between melt and crystals, and a major goal is to explain how this might result in chemical differentiation of magma. Arriving at a full description of the physics of crystallizing magma chambers is a challenge because of the large number of processes potentially involved, the many coupled variables, and the different geometrical shapes. Furthermore, perturbations are caused by the reinjection of melt from a deep source, eruption to the Earth's surface, and the assimilation of country rock. Physical models of increasing complexity have been developed with emphasis on three fundamental approaches. One is, given that large gradients in temperature and composition may occur, to specify how to apply thermodynamic constraints so that coexisting liquid and solid compositions may be calculated. The second is to leave the differentiation trend as the solution to be found, i.e., to specify how cooling occurs and to predict the evolution of the composition of the residual liquid and of the solid forming. The third is to simplify the physics so that the effects of coupled heat and mass transfer may be studied with a reduced set of variables. The complex shapes of magma chambers imply that boundary layers develop with density gradients at various angles to gravity, leading to various convective flows and profiles qf liquid stratification. Early studies were mainly concerned with describing fluid flow in the liquid interior of large reservoirs, due to gradients developed at the margins. More recent work has focused on the internal structure and flow field of boundary layers and in particular on the gradients of solid fraction and interstitial melt composition which develop within them. Crystal settling may occur in a surprisingly diverse range of regimes and may lead to intermittent deposition

Melt inclusions: Chapter 6

Science.gov (United States)

,; Lowenstern, J. B.

2014-01-01

Melt inclusions are small droplets of silicate melt that are trapped in minerals during their growth in a magma. Once formed, they commonly retain much of their initial composition (with some exceptions) unless they are re-opened at some later stage. Melt inclusions thus offer several key advantages over whole rock samples: (i) they record pristine concentrations of volatiles and metals that are usually lost during magma solidification and degassing, (ii) they are snapshots in time whereas whole rocks are the time-integrated end products, thus allowing a more detailed, time-resolved view into magmatic processes (iii) they are largely unaffected by subsolidus alteration. Due to these characteristics, melt inclusions are an ideal tool to study the evolution of mineralized magma systems. This chapter first discusses general aspects of melt inclusions formation and methods for their investigation, before reviewing studies performed on mineralized magma systems.

Lithospheric magma dynamics beneath the El Hierro Volcano, Canary Islands: insights from fluid inclusions

Science.gov (United States)

Oglialoro, E.; Frezzotti, M. L.; Ferrando, S.; Tiraboschi, C.; Principe, C.; Groppelli, G.; Villa, I. M.

2017-10-01

At active volcanoes, petrological studies have been proven to be a reliable approach in defining the depth conditions of magma transport and storage in both the mantle and the crust. Based on fluid inclusion and mineral geothermobarometry in mantle xenoliths, we propose a model for the magma plumbing system of the Island of El Hierro (Canary Islands). The peridotites studied here were entrained in a lava flow exposed in the El Yulan Valley. These lavas are part of the rift volcanism that occurred on El Hierro at approximately 40-30 ka. The peridotites are spinel lherzolites, harzburgites, and dunites which equilibrated in the shallow mantle at pressures between 1.5 and 2 GPa and at temperatures between 800 and 950 °C (low-temperature peridotites; LT), as well as at higher equilibration temperatures of 900 to 1100 °C (high-temperature peridotites; HT). Microthermometry and Raman analyses of fluid inclusions reveal trapping of two distinct fluid phases: early type I metasomatic CO2-N2 fluids ( X N2 = 0.01-0.18; fluid density (d) = 1.19 g/cm3), coexisting with silicate-carbonate melts in LT peridotites, and late type II pure CO2 fluids in both LT (d = 1.11-1.00 and 0.75-0.65 g/cm3) and HT ( d = 1.04-1.11 and 0.75-0.65 g/cm3) peridotites. While type I fluids represent metasomatic phases in the deep oceanic lithosphere (at depths of 60-65 km) before the onset of magmatic activity, type II CO2 fluids testify to two fluid trapping episodes during the ascent of xenoliths in their host mafic magmas. Identification of magma accumulation zones through interpretation of type II CO2 fluid inclusions and mineral geothermobarometry indicate the presence of a vertically stacked system of interconnected small magma reservoirs in the shallow lithospheric mantle between a depth of 22 and 36 km (or 0.67 to 1 GPa). This magma accumulation region fed a short-lived magma storage region located in the lower oceanic crust at a depth of 10-12 km (or 0.26-0.34 GPa). Following our model

Geodynamics of kimberlites on a cooling Earth: Clues to plate tectonic evolution and deep volatile cycles

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Tappe, Sebastian; Smart, Katie; Torsvik, Trond; Massuyeau, Malcolm; de Wit, Mike

2018-02-01

Kimberlite magmatism has occurred in cratonic regions on every continent. The global age distribution suggests that this form of mantle melting has been more prominent after 1.2 Ga, and notably between 250-50 Ma, than during early Earth history before 2 Ga (i.e., the Paleoproterozoic and Archean). Although preservation bias has been discussed as a possible reason for the skewed kimberlite age distribution, new treatment of an updated global database suggests that the apparent secular evolution of kimberlite and related CO2-rich ultramafic magmatism is genuine and probably coupled to lowering temperatures of Earth's upper mantle through time. Incipient melting near the CO2- and H2O-bearing peridotite solidus at >200 km depth (1100-1400 °C) is the petrologically most feasible process that can produce high-MgO carbonated silicate melts with enriched trace element concentrations akin to kimberlites. These conditions occur within the convecting asthenospheric mantle directly beneath thick continental lithosphere. In this transient upper mantle source region, variable CHO volatile mixtures control melting of peridotite in the absence of heat anomalies so that low-degree carbonated silicate melts may be permanently present at ambient mantle temperatures below 1400 °C. However, extraction of low-volume melts to Earth's surface requires tectonic triggers. Abrupt changes in the speed and direction of plate motions, such as typified by the dynamics of supercontinent cycles, can be effective in the creation of lithospheric pathways aiding kimberlite magma ascent. Provided that CO2- and H2O-fluxed deep cratonic keels, which formed parts of larger drifting tectonic plates, existed by 3 Ga or even before, kimberlite volcanism could have been frequent during the Archean. However, we argue that frequent kimberlite magmatism had to await establishment of an incipient melting regime beneath the maturing continents, which only became significant after secular mantle cooling to below

Magma reservoir dynamics at Toba caldera, Indonesia, recorded by oxygen isotope zoning in quartz.

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Budd, David A; Troll, Valentin R; Deegan, Frances M; Jolis, Ester M; Smith, Victoria C; Whitehouse, Martin J; Harris, Chris; Freda, Carmela; Hilton, David R; Halldórsson, Sæmundur A; Bindeman, Ilya N

2017-01-25

Quartz is a common phase in high-silica igneous rocks and is resistant to post-eruptive alteration, thus offering a reliable record of magmatic processes in silicic magma systems. Here we employ the 75 ka Toba super-eruption as a case study to show that quartz can resolve late-stage temporal changes in magmatic δ 18 O values. Overall, Toba quartz crystals exhibit comparatively high δ 18 O values, up to 10.2‰, due to magma residence within, and assimilation of, local granite basement. However, some 40% of the analysed quartz crystals display a decrease in δ 18 O values in outermost growth zones compared to their cores, with values as low as 6.7‰ (maximum ∆ core-rim  = 1.8‰). These lower values are consistent with the limited zircon record available for Toba, and the crystallisation history of Toba quartz traces an influx of a low-δ 18 O component into the magma reservoir just prior to eruption. Here we argue that this late-stage low-δ 18 O component is derived from hydrothermally-altered roof material. Our study demonstrates that quartz isotope stratigraphy can resolve magmatic events that may remain undetected by whole-rock or zircon isotope studies, and that assimilation of altered roof material may represent a viable eruption trigger in large Toba-style magmatic systems.

Effect of pressure on Fe3+/ΣFe ratio in a mafic magma and consequences for magma ocean redox gradients

Energy Technology Data Exchange (ETDEWEB)

Zhang, H. L.; Hirschmann, M. M.; Cottrell, E.; Withers, A. C.

2017-05-01

Experiments establishing the effect of pressure on the Fe³⁺/ΣFe ratio of andesitic silicate melts buffered by coexisting Ru and RuO₂ were performed from 100 kPa to 7 GPa and 1400–1750 °C. Fe³⁺/ΣFe ratios were determined by room temperature Mössbauer spectroscopy, but corrected for the effects of recoilless fraction. Fe³⁺/ΣFe ratios in quenched glasses decrease with increasing pressure consistent with previous results between 100 kPa and 3 GPa (O’Neill et al., 2006), but show only small pressure effects above 5 GPa. Ratios also decrease with increasing temperature. Mössbauer hyperfine parameters indicate mean coordination of Fe³⁺ ions of ~5 in glasses, with no dependence on the pressure from which the glasses were quenched, but show an increase with pressure in mean coordination of Fe²⁺ ions, from ~5 to ~6. XANES spectra on these glasses show variations in pre-edge intensities and centroid positions that are systematic with Fe³⁺/ΣFe, but are displaced from those established from otherwise identical andesitic glasses quenched at 100 kPa (Zhang et al., 2016). These systematics permit construction of a new XANES calibration curve relating pre-edge sub-peak intensities to Fe³⁺/ΣFe applicable to high pressure glasses. Consistent with interpretations of the Mössbauer hyperfine parameters, XANES pre-edge peak features in high pressure glasses are owing chiefly to the effects of pressure on the coordination of Fe²⁺ ions from ~5.5 to ~6, with negligible effects evident for Fe³⁺ ions. We use the new data to construct a thermodynamic model relating the effects of oxygen fugacity and pressure on Fe³⁺/ΣFe. We apply this model to calculate variations in oxygen fugacity in isochemical (constant Fe³⁺/ΣFe) columns of magma representative of magma oceans, in which fO2 is fixed at the base by equilibration with molten Fe. These calculations

Characterization and nutrient release from silicate rocks and influence on chemical changes in soil

Directory of Open Access Journals (Sweden)

Douglas Ramos Guelfi Silva

2012-06-01

Full Text Available The expansion of Brazilian agriculture has led to a heavy dependence on imported fertilizers to ensure the supply of the growing food demand. This fact has contributed to a growing interest in alternative nutrient sources, such as ground silicate rocks. It is necessary, however, to know the potential of nutrient release and changes these materials can cause in soils. The purpose of this study was to characterize six silicate rocks and evaluate their effects on the chemical properties of treated soil, assessed by chemical extractants after greenhouse incubation. The experimental design consisted of completely randomized plots, in a 3 x 6 factorial scheme, with four replications. The factors were potassium levels (0-control: without silicate rock application; 200; 400; 600 kg ha-1 of K2O, supplied as six silicate rock types (breccia, biotite schist, ultramafic rock, phlogopite schist and two types of mining waste. The chemical, physical and mineralogical properties of the alternative rock fertilizers were characterized. Treatments were applied to a dystrophic Red-Yellow Oxisol (Ferralsol, which was incubated for 100 days, at 70 % (w/w moisture in 3.7 kg/pots. The soil was evaluated for pH; calcium and magnesium were extracted with KCl 1 mol L-1; potassium, phosphorus and sodium by Mehlich 1; nickel, copper and zinc with DTPA; and the saturation of the cation exchange capacity was calculated for aluminum, calcium, magnesium, potassium, and sodium, and overall base saturation. The alternative fertilizers affected soil chemical properties. Ultramafic rock and Chapada mining byproduct (CMB were the silicate rocks that most influenced soil pH, while the mining byproduct (MB led to high K levels. Zinc availability was highest in the treatments with mining byproduct and Cu in soil fertilized with Chapada and mining byproduct.

Transport of metals and sulphur in magmas by flotation of sulphide melt on vapour bubbles

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Mungall, J. E.; Brenan, J. M.; Godel, B.; Barnes, S. J.; Gaillard, F.

2015-03-01

Emissions of sulphur and metals from magmas in Earth’s shallow crust can have global impacts on human society. Sulphur-bearing gases emitted into the atmosphere during volcanic eruptions affect climate, and metals and sulphur can accumulate in the crust above a magma reservoir to form giant copper and gold ore deposits, as well as massive sulphur anomalies. The volumes of sulphur and metals that accumulate in the crust over time exceed the amounts that could have been derived from an isolated magma reservoir. They are instead thought to come from injections of multiple new batches of vapour- and sulphide-saturated magmas into the existing reservoirs. However, the mechanism for the selective upward transfer of sulphur and metals is poorly understood because their main carrier phase, sulphide melt, is dense and is assumed to settle to the bottoms of magma reservoirs. Here we use laboratory experiments as well as gas-speciation and mass-balance models to show that droplets of sulphide melt can attach to vapour bubbles to form compound drops that float. We demonstrate the feasibility of this mechanism for the upward mobility of sulphide liquids to the shallow crust. Our work provides a mechanism for the atmospheric release of large amounts of sulphur, and contradicts the widely held assumption that dense sulphide liquids rich in sulphur, copper and gold will remain sequestered in the deep crust.

Metal/silicate partitioning of Pt and the origin of the "late veneer"

Science.gov (United States)

Ertel, W.; Walter, M. J.; Drake, M. J.; Sylvester, P. J.

2002-12-01

the melting point of the 1 atm, AnDi system and the melting point of the Pt capsule material. Over 150 piston cylinder and 12 multi anvil experiments have been performed. Pt solubility is only slightly dependent on temperature, decreasing between 1800 and 1400°C by less than an order of magnitude. In consequence, the partitioning behavior of Pt is mostly determined by its oxygen fugacity dependence, which has only been determined in 1 atm experiments. At 10 kbar, metal/silicate partition coefficients (D's) decrease by about 3 orders of magnitude. The reason for this is not understood, but might be attributed to a first order phase transition as found for, e.g., SiO2 or H2O. Above 10 kbar any increase in pressure does not lead to any further significant decrease in partition coefficients. Solubilities stay roughly constant up to 140 kbar. Abundances of moderately siderophile elements were possibly established by metal/silicate equilibrium in a magma ocean. These results for Pt suggest that the abundances of HSEs were most probably established by the accretion of a chondritic veneer following core formation, as metal/silicate partition coefficients are too high to be consistent with metal/silicate equilibrium in a magma ocean.

The Meaning of "Magma"

Science.gov (United States)

Bartley, J. M.; Glazner, A. F.; Coleman, D. S.

2016-12-01

Magma is a fundamental constituent of the Earth, and its properties, origin, evolution, and significance bear on issues ranging from volcanic hazards to planetary evolution. Unfortunately, published usages indicate that the term "magma" means distinctly different things to different people and this can lead to miscommunication among Earth scientists and between scientists and the public. Erupting lava clearly is magma; the question is whether partially molten rock imaged at depth and too crystal-rich to flow should also be called magma. At crystal fractions > 50%, flow can only occur via crystal deformation and solution-reprecipitation. As the solid fraction increases to 90% or more, the material becomes a welded crystal framework with melt in dispersed pores and/or along grain boundaries. Seismic images commonly describe such volumes of a few % melt as magma, yet the rheological differences between melt-rich and melt-poor materials make it vital not to confuse a large rock volume that contains a small melt fraction with melt-rich material. To ensure this, we suggest that "magma" be reserved for melt-rich materials that undergo bulk fluid flow on timescales consonant with volcanic eruptions. Other terms should be used for more crystal-rich and largely immobile partially molten rock (e.g., "crystal mush," "rigid sponge"). The distinction is imprecise but useful. For the press, the public, and even earth scientists who do not study magmatic systems, "magma" conjures up flowing lava; reports of a large "magma" body that contains a few percent melt can engender the mistaken perception of a vast amount of eruptible magma. For researchers, physical processes like crystal settling are commonly invoked to account for features in plutonic rocks, but many such processes are only possible in melt-rich materials.

Emplacement model of obsidian-rhyolite magma deduced from complete internal section of the Akaishiyama lava, Shirataki, northern Hokkaido, Japan

Science.gov (United States)

Wada, K.; Sano, K.

2016-12-01

Simultaneously explosive and effusive eruptions of silicic magmas has shed light on the vesiculation and outgassing history of ascending magmas in the conduit and emplacement model of obsidian-rhyolite lavas (Castro et al., 2014; Shipper et al, 2013). As well as the knowledge of newly erupted products such as 2008-2009 Chaitén and 2011-2012 Cordón Caule eruptions, field and micro-textural evidences of well-exposed internal structure of obsidian-rhyolite lava leads to reveal eruption processes of silicic magmas. The Shirataki monogenetic volcano field, 2.2 million year age, northern Hokkaido, Japan, contains many outcrops of obsidian and vesiculated rhyolite zones (SiO2=76.7-77.4 wt.%). Among their outcrops, Akaishiyama lava shows good exposures of internal sections from the top to the bottom along the Kyukasawa valley with thickness of about 190 meters, showing the symmetrical structure comprising a upper clastic zone (UCZ; 5m thick), an upper dense obsidian zone (UDO; 15m), an upper banded obsidian zone (UBO; 70-80m), a central rhyolite zone (CR; 65m), a lower banded obsidian zone (LBO; 15m), a lower dense obsidian zone (LDO; 20m), and a lower clastic zone (LCZ; 3m). The upper banded obsidian zone is characterized by existence of spherulite concentration layers with tuffisite veins and rhyolite enclaves. Spherulites consisting of albite, cristobalaite and obsidian glass, are clustered in the dense obsidian. Tuffisite veins show brecciated obsidians in tuffaceous matrix, showing an outgassing path during the emplacement of obsidian lava. Perpendicular dip of spherulite parallel rows indicates the banded zone itself was the domain of vent area. From the observation of these occurrences in the internal section and rock texture, we show the qualitative formation model of Shirataki obsidian-rhyolite lava.

Platinum-bearing chromite layers are caused by pressure reduction during magma ascent.

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Latypov, Rais; Costin, Gelu; Chistyakova, Sofya; Hunt, Emma J; Mukherjee, Ria; Naldrett, Tony

2018-01-31

Platinum-bearing chromitites in mafic-ultramafic intrusions such as the Bushveld Complex are key repositories of strategically important metals for human society. Basaltic melts saturated in chromite alone are crucial to their generation, but the origin of such melts is controversial. One concept holds that they are produced by processes operating within the magma chamber, whereas another argues that melts entering the chamber were already saturated in chromite. Here we address the problem by examining the pressure-related changes in the topology of a Mg 2 SiO 4 -CaAl 2 Si 2 O 8 -SiO 2 -MgCr 2 O 4 quaternary system and by thermodynamic modelling of crystallisation sequences of basaltic melts at 1-10 kbar pressures. We show that basaltic melts located adjacent to a so-called chromite topological trough in deep-seated reservoirs become saturated in chromite alone upon their ascent towards the Earth's surface and subsequent cooling in shallow-level chambers. Large volumes of these chromite-only-saturated melts replenishing these chambers are responsible for monomineralic layers of massive chromitites with associated platinum-group elements.

The effect of pressurized magma chamber growth on melt migration and pre-caldera vent locations through time at Mount Mazama, Crater Lake, Oregon

Science.gov (United States)

Karlstrom, Leif; Wright, Heather M.; Bacon, Charles R.

2015-01-01

The pattern of eruptions at long-lived volcanic centers provides a window into the co-evolution of crustal magma transport, tectonic stresses, and unsteady magma generation at depth. Mount Mazama in the Oregon Cascades has seen variable activity over the last 400 ky, including the 50 km3 climactic eruption at ca. 7.7 ka that produced Crater Lake caldera. The physical mechanisms responsible for the assembly of silicic magma reservoirs that are the precursors to caldera-forming eruptions are poorly understood. Here we argue that the spatial and temporal distribution of geographically clustered volcanic vents near Mazama reflects the development of a centralized magma chamber that fed the climactic eruption. Time-averaged eruption rates at Mount Mazama imply an order of magnitude increase in deep magma influx prior to the caldera-forming event, suggesting that unsteady mantle melting triggered a chamber growth episode that culminated in caldera formation. We model magma chamber–dike interactions over ∼50 ky preceding the climactic eruption to fit the observed distribution of surface eruptive vents in space and time, as well as petrologically estimated deep influx rates. Best fitting models predict an expanding zone of dike capture caused by a growing, oblate spheroidal magma chamber with 10–30 MPa of overpressure. This growing zone of chamber influence causes closest approaching regional mafic vent locations as well as more compositionally evolved Mazama eruptions to migrate away from the climactic eruptive center, returning as observed to the center after the chamber drains during the caldera-forming eruption.

The Thickness of the Mushy Layer on the Floor of the Skaergaard Magma Chamber at Apatite Saturation

DEFF Research Database (Denmark)

Holness, Marian B.; Tegner, Christian; Nielsen, Troels F. D.

2017-01-01

We present a novel way of constraining the thickness of the crystal mush in fractionated layered intrusions using detailed microstructural analysis. The results are combined with geochemical data to create a snapshot of the crystal mush on the floor of the Skaergaard magma chamber in the period i...

Improving Student Understanding of Magmatic Differentiation Using an M&M Magma Chamber

Science.gov (United States)

Wirth, K. R.

2003-12-01

Many students, especially those in introductory geology courses, have difficulty developing a deep understanding of the processes of magmatic differentiation. In particular, students often struggle to understand Bowen's reaction series and fractional crystallization. The process of fractional crystallization by gravity settling can be illustrated using a model magma chamber consisting of M&M's. In this model, each major cation (e.g., Si, Ti, Al, Fe, Mg, Ca, Na, K) is represented by a different color M&M; other kinds of differently colored or shaped pieces could also be used. Appropriate numbers of each color M&M are combined to approximate the cation proportions of a basaltic magma. Students then fractionate the magma by moving M&M's to the bottom of the magma chamber forming a series of cumulus layers; the M&M's are removed in the stoichiometric proportions of cations in the crystallizing minerals (e.g., olivine, pyroxene, feldspars, quartz, magnetite, ilmenite). Students observe the changing cation composition (proportions of colors of M&M's) in the cumulus layers and in the magma chamber and graph the results using spreadsheet software. More advanced students (e.g., petrology course) can classify the cumulates and resulting liquid after each crystallization step, and they can compare the model system with natural magmatic systems (e.g., absence of important fractionating phases, volatiles). Students who have completed this exercise generally indicate a positive experience and demonstrate increased understanding of Bowen's reaction series and fractionation processes. They also exhibit greater familiarity with mineral stoichiometry, classification, solid-solution in minerals, element behavior (e.g., incompatibility), and chemical variation diagrams. Other models (e.g., paths of equilibrium and fractional crystallization on phase diagrams) can also be used to illustrate differentiation processes in upper level courses (e.g., mineralogy and petrology).

Oxidation State of Iron in the Izu-Bonin Arc Initial Magma and Its Influence Factors

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Li, H.; Arculus, R. J.; Brandl, P. A.; Hamada, M.; Savov, I. P.; Zhu, S.; Hickey-Vargas, R.; Tepley, F. J., III; Meffre, S.; Yogodzinski, G. M.; McCarthy, A.; Barth, A. P.; Kanayama, K.; Kusano, Y.; Sun, W.

2014-12-01

The redox state of mantle-derived magmas is a controversial issue, especially whether island arc basalts are more oxidized than those from mid-ocean ridges. Usually, arc magmas have higher Fe3+/Fe2+ and calculated oxygen fugacity (fO2) than mid-ocean ridge basalts (MORB). It is the high fO2 of arc magma that apparently delays onset of sulfide fractionation and sequestration of precious/base metals thereby facilitating the formation of many giant gold-copper deposits typically associated with subduction zones. But due to a paucity of Fe3+/Fe2+ data for primary mantle-derived arc magmas, the cause for high fO2 of these magma types is still controversial; causes may include inter alia subduction-released oxidized material addition to the mantle wedge source of arc magma, partial melting of subducted slab, and redox changes occurring during ascent of the magma. Fortunately, IODP expedition 351 drilling at IODP Site U1438 in the Amami-Sankaku Basin of the northwestern Philipine Sea, adjacent to the proto-Izu-Bonin Arc at the Kyushu-Palau Ridge (KPR), recovered not only volcaniclastics derived from the inception of Izu-Bonin Mariana (IBM) arc in the Eocene, but also similar materials for the Arc's subsequent evolution through to the Late Oligocene and abandonment of the KPR as a remnant arc. Samples of the pre-Arc oceanic crustal basement were also recovered enabling us to determine the fO2of the mantle preceding arc inception. As the oxidation state of iron in basaltic glass directly relates to the fO2 , the Fe3+/∑Fe ratio [Fe3+/(Fe3++ Fe2+)] of basaltic glass are quantified by synchrotron-facilitated micro X-ray Absorption Near Edge Structure (XANES) spectroscopy to reflect its fO2. Fe K-edge µ-XANES spectra were recorded in fluorescence mode at Beamline 15U1, Shanghai Synchrotron Radiation Facility (SSRF). Synthetic silicate glass with known Fe3+/∑Fe ratio was used in data handling. The experimental results as well as preliminary data from IODP Expedition 351

Silicic melt evolution in the early Izu-Bonin arc recorded in detrital zircons: Zircon U-Pb geochronology and trace element geochemistry for Site U1438, Amami Sankaku Basin

Science.gov (United States)

Barth, A. P.; Tani, K.; Meffre, S.; Wooden, J. L.; Coble, M. A.

2016-12-01

Understanding the petrologic evolution of oceanic arc magmas through time is important because these arcs reveal the processes of formation and the early evolution of juvenile continental crust. The Izu-Bonin (IB) arc system has been targeted because it is one of several western Pacific intraoceanic arcs initiated at 50 Ma and because of its prominent spatial asymmetry, with widespread development of relatively enriched rear arc lavas. We examined Pb/U and trace element compositions in zircons recovered at IODP Site 351-U1438 and compared them to regional and global zircon suites. These new arc zircon data indicate that detrital zircons will yield new insights into the generation of IB silicic melts and form a set of useful geochemical proxies for interpreting ancient arc detrital zircon provenance. Project IBM drilling target IBM1 was explored by Expedition 351 at Site U1438, located in the proximal back-arc of the northern Kyushu-Palau Ridge (KPR) at 27.3°N. A 1.2 km thick section of Paleogene volcaniclastic rocks, increasingly lithified and hydrothermally altered with depth, constitutes a proximal rear arc sedimentary record of IB arc initiation and early arc evolution. The ages and compositions of U1438 zircons are compatible with provenance in one or more edifices of the northern KPR and are incompatible with drilling contamination. Melt zircon saturation temperatures and Ti-in-zircon thermometry suggest a provenance in relatively cool and silicic KPR melts. The abundances of selected trace elements with high native concentrations provide insight into the petrogenesis of U1438 detrital zircon host melts, and may be useful indicators of both short and long-term variations in melt compositions in arc settings. The U1438 zircons are slightly enriched in U and LREE and are depleted in Nb compared to zircons from mid-ocean ridges and the Parece-Vela Basin, as predicted for melts in a primitive oceanic arc setting with magmas derived from a highly depleted mantle

Petrological cycles and caldera-forming events

Science.gov (United States)

Bachmann, O.; Deering, C. D.

2012-12-01

Many caldera-forming events can be framed within broad petrological cycles; volcanic stratigraphy typically defines a trend from mafic to more silicic magmas with time, culminating in the catastrophic evacuation of an upper crustal reservoir filled with the silicic magma, followed by a return to the eruption of more mafic magmas shortly after caldera collapse. Understanding how such cycles develop has clear implications for characterizing the current state of an active system. Here, we focus on a detailed examination of the well-exposed Quaternary Kos-Nisyros eruptive sequence (eastern Aegean arc) to frame a potential model for such cycles. On the basis of zircon U/Th/Pb ages, building the upper crustal magma chamber large enough to induce caldera collapse required at least a few hundred thousand years. This timeframe is necessary not only for the accumulation of large amounts of viscous, gas-rich silicic magma, but also to heat the upper crust sufficiently to allow the developing reservoir to be maintained above the solidus. In the Kos-Nisyros volcanic center, small eruptions precede the caldera-forming event and mark this period of thermal maturation as the system transitions from intermediate to silicic magma, reaching the most-evolved state only shortly prior to the caldera-forming event, the Kos Plateau Tuff (> 60 km3 of volatile-rich, high-silica rhyolite). The Kos Plateau Tuff was then followed by small-volume eruptions of more mafic magma (basaltic andesite, andesite, and dacites) that are characterized by a drier mineral assemblage. With time, the system transitioned back to cold, wet, high-SiO2 rhyolite. We suggest that the changes in magma composition and mineralogy following the caldera-forming event are due to a near-complete crystallization of the non-erupted mush in the upper crustal reservoir as it is abruptly decompressed during eruption. This rapid crystallization (1) leads to the formation of a porphyritic texture in the crystalline residual - a

Moonage Daydream: Reassessing the Simple Model for Lunar Magma Ocean Crystallization

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Rapp, J. F.; Draper, D. S.

2016-01-01

Details of the differentiation of a global-scale lunar magma ocean (LMO) remain enigmatic, as the Moon is not simply composed of highlands anorthosite and a suite of mare basalts as inferred from early studies. Results from recent orbital missions, and the increasingly detailed study of lunar samples, have revealed a much larger range of lithologies, from relatively MgO-rich and "purest anorthosite" discovered on the lunar far side by the M3 instrument on Chandraayan-1 to more exotic lithologies such as Si-rich domes and spinel-rich clasts distributed globally. To understand this increasingly complex geology, we must understand the initial formation and evolution of the LMO, and the composition of the cumulates this differentiation could have produced. Several attempts at modelling such a crystallization sequence have been made, and have raised as many questions as they have answered. We present results from our ongoing experimental simulations of magma ocean crystallization, investigating two end-member bulk compositions (TWM and LPUM) under fully fractional crystallization conditions. These simulations represent melting of the entire silicate portion of the Moon, as an end-member starting point from which to begin assessing the evolution of the lunar interior and formation of the lunar crust.

Constraint on the magma sources in Luzon Island Philippines by using P and S wave local seismic tomography

Science.gov (United States)

Nghia, N. C.; Huang, B. S.; Chen, P. F.

2017-12-01

The subduction of South China Sea beneath the Luzon Island has caused a complex setting of seismicity and magmatism because of the proposed ridge subduction and slab tearing. To constrain the validity of slab tearing induced by ridge subduction and their effect, we performed a P and S wave seismic tomography travel time inversion using LOTOS code. The dataset has been retrieved from International Seismological Centre from 1960 to 2008. A 1D velocity inverted by using VELEST with a Vp/Vs ratio of 1.74 is used as the starting input velocity for tomographic inversion. Total of 20905 P readings and 8126 S readings from 2355 earthquakes events were used to invert for velocity structure beneath Luzon Island. The horizontal tomographic results show low-velocity, high Vp/Vs regions at the shallow depth less than 50 km which are interpreted as the magmatic chambers of the volcanic system in Luzon. At the suspected region of slab tearing at 16oN to 18oN, two sources of magma have been indentified: slab window magma at shallow depth (< 50 km) and magma induced by mantle wedge partial melting from higher depth. This slab melting may have changed the composition of magmatic to become more silicic with high viscosity, which explains the volcanic gap in this region. At the region of 14oN to 15oN, large magma chambers under active volcanos are identified which explain the active volcanism in this region. Contrast to the region of slab tearing, in this region, the magma chambers are fed by only magma from partial melting of mantle wedge from the depth higher than 100 km. These observations are consistent with previous work on the slab tearing of South China Sea and the activities of volcanism in the Luzon Island.

Geochemical evidences of magma dynamics at Campi Flegrei (Italy)

Science.gov (United States)

Caliro, S.; Chiodini, G.; Paonita, A.

2014-05-01

Campi Flegrei caldera, within the Neapolitan area of Italy, is potentially one of the most dangerous volcanoes in the world, and during the last decade it has shown clear signs of reactivation, marked by the onset of uplift and changes in the geochemistry of gas emissions. We describe a 30-year-long data set of the CO2-He-Ar-N2 compositions of fumarolic emissions from La Solfatara crater, which is located in the center of the caldera. The data display continuous decreases in both the N2/He and N2/CO2 ratios since 1985, paralleled by an increase in He/CO2. These variations cannot be explained by either processes of boiling/condensation in the local hydrothermal system or with changes in the mixing proportions between a magmatic vapor and hydrothermal fluids. We applied the magma degassing model of Nuccio and Paonita (2001, Earth Planet. Sci. Lett. 193, 467-481) using the most recent inert-gas solubilities in order to interpret these peculiar features in accordance with petrologic constraints derived from the ranges of the melt compositions and reservoir pressures at Campi Flegrei. The model simulations for mafic melts (trachybasalt and shoshonite) show a remarkably good agreement with the measured data. Both decompressive degassing of an ascending magma and mixing between magmatic fluids exsolved at various levels along the ascent path can explain the long-term geochemical changes. Recalling that (i) a sill-like reservoir of gases at a depth of 3-4 km seems to be the main source of ground inflation and (ii) there is petrologic and geophysical evidence for a reservoir of magma at about 8 km below Campi Flegrei, we suggest that the most-intense episodes of inflation occur when the gas supply to the sill-like reservoir comes from the 8 km-deep magma, although fluids exsolved by magma bodies at shallower depths also contribute to the gas budget. Our work highlights that, in caldera systems where the presence of hydrothermal aquifers commonly masks the magmatic signature

It's the little things that matter most: The role of volatiles in volcanoes and their magmatic roots

Science.gov (United States)

Keller, T.; Suckale, J.

2017-12-01

Many volcanic eruptions are driven by volatiles - mostly H2O and CO2 - that degas from magmas rising up beneath the volcano. Gas expands during ascent, thus frequently creating lavas with upward of 50% vesicularity. That is a particularly compelling observation considering that volatiles are only present at concentrations of order 100 ppm in the mantle source. Yet, even at these small concentrations, volatiles significantly lower the peridotite solidus. That leads to the production of reactive volatile-rich melts at depth, which has important consequences for melt transport in the asthenosphere. Thus, volatiles have a pivotal role both at the beginning and the end of the magmatic storyline. A growing amount of observational evidence provides various perspectives on these systems. Volcanic products are characterised increasingly well by geochemical and petrological data. And, volcano monitoring now often provides continuous records of degassing flux and composition. What is missing to better interpret these data are coupled fluid mechanic and thermodynamic models that link melt production and reactive transport in the mantle and crust with degassing-driven volcanic activity at the surface. Such models need to describe the deformation and segregation of multiple material phases (liquids, solids, gases) and track the reactive transport of diverse chemical components (major elements, trace elements, volatiles). I will present progress towards a generalization of existing two-phase model for melt transport in the mantle, extending them to three-phase flows appropriate for magma circulation and degassing in volcanoes. What sets the two environments apart is the presence of a compressible vapor in volcanoes. Also, volcanic degassing may occur by convecting suspensions as well as porous segregation. The model framework we are developing for these processes is based on mixture theory. Uncovering the underlying physics that connects these diverse expressions of magma

No effect of H2O degassing on the oxidation state of hydrous rhyolite magmas: a comparison of pre- and post-eruptive Fe2+ concentrations in six obsidian samples from the Mexican and Cascade arcs

Science.gov (United States)

Waters, L.; Lange, R. A.

2011-12-01

The extent to which degassing affects the oxidation state of arc magmas is widely debated. Several researchers have examined how degassing of mixed H-C-O-S-Cl fluids may change the Fe3+/FeT ratio of magmas, and it has been proposed that degassing may induce either oxidation or reduction depending on the initial oxidation state. A commonly proposed oxidation reaction is related to H2O degassing: H2O (melt) + 2FeO (melt) = H2 (fluid) + Fe2O3 (melt). Another mechanism by which H2O degassing can affect the iron redox state is if dissolved water affects the activity of ferrous and/or ferric iron in the melt. Although Moore et al. (1995) presented experiments showing no evidence of an affect of dissolved water on the activity of the ferric-ferrous ratio in silicate melts, other experimental results (e.g., Baker and Rutherford, 1996; Gaillard et al., 2001; 2003) indicate that there may be such an effect in rhyolite liquids. It has long been understood that rhyolites, owing to their low total iron concentrations, are more sensitive than other magma types to degassing-induced change in redox state. Therefore, a rigorous test of whether H2O degassing affects the redox state of arc magmas is best evaluated on rhyolites. In this study, a comparison is made between the pre-eruptive (pre-degassing) Fe2+ concentrations in six, phenocryst-poor (volatiles, as indicated by the low loss on ignition values (LOI ≤ 0.7 wt%). In order to test how much oxidation of ferrous iron occurred as a consequence of that degassing, we measured the ferrous iron concentration in the bulk samples by titration, using the Wilson (1960) method, which was successfully tested again three USGS and one Canadian Geological Survey standards. Our results indicate no detectable change within analytical error between pre- and post-eruptive FeO concentrations, with an average deviation of 0.09 wt% and a maximum deviation of 0.15 wt%. Our results show that H2O degassing has no effect on the redox state of

The Earth’s mantle before convection: Effects of magma oceans and the Moon (Invited)

Science.gov (United States)

Elkins-Tanton, L. T.; Smrekar, S. E.; Tobie, G.

2009-12-01

thick solid lid and diminished the likelihood of mantle remixing. Second, on an Earth-sized planet a magma ocean would solidify to produce very dense near-surface solids that also contain the bulk of the water held in the solid state, and the bulk of the incompatible elements. During gravitationally-driven overturn shallow, dense, damp solids carry their water as they sink into the perovskite stability zone and transform the bulk of their mineralogy into perovskite. The last solids that form near the surface exceed the likely water saturation levels of perovskite and will be forced to dewater as they cross the boundary into the lower mantle, leaving water behind in a rapid flux as the dense material sinks. This event will form a kind of “water catastrophe,” and would have the potential to partially melt the upper mantle, to produce a damp asthensosphere, and indeed to encourage convection. These results imply that planets in which perovskite is stable, that is, planets that are larger than Mars, are perhaps more likely to have an early initiation of plate tectonics, and that larger planets may have more violent and near-surface mantle volatile releases during any overturn event.

Long-Term Volumetric Eruption Rates and Magma Budgets

Energy Technology Data Exchange (ETDEWEB)

Scott M. White Dept. Geological Sciences University of South Carolina Columbia, SC 29208; Joy A. Crisp Jet Propulsion Laboratory, California Institute of Technology Pasadena, CA 91109; Frank J. Spera Dept. Earth Science University of California, Santa Barbara Santa Barbara, CA 93106

2005-01-01

A global compilation of 170 time-averaged volumetric volcanic output rates (Qe) is evaluated in terms of composition and petrotectonic setting to advance the understanding of long-term rates of magma generation and eruption on Earth. Repose periods between successive eruptions at a given site and intrusive:extrusive ratios were compiled for selected volcanic centers where long-term (>104 years) data were available. More silicic compositions, rhyolites and andesites, have a more limited range of eruption rates than basalts. Even when high Qe values contributed by flood basalts (9 ± 2 Å~ 10-1 km3/yr) are removed, there is a trend in decreasing average Qe with lava composition from basaltic eruptions (2.6 ± 1.0 Å~ 10-2 km3/yr) to andesites (2.3 ± 0.8 Å~ 10-3 km3/yr) and rhyolites (4.0 ± 1.4 Å~ 10-3 km3/yr). This trend is also seen in the difference between oceanic and continental settings, as eruptions on oceanic crust tend to be predominately basaltic. All of the volcanoes occurring in oceanic settings fail to have statistically different mean Qe and have an overall average of 2.8 ± 0.4 Å~ 10-2 km3/yr, excluding flood basalts. Likewise, all of the volcanoes on continental crust also fail to have statistically different mean Qe and have an overall average of 4.4 ± 0.8 Å~ 10-3 km3/yr. Flood basalts also form a distinctive class with an average Qe nearly two orders of magnitude higher than any other class. However, we have found no systematic evidence linking increased intrusive:extrusive ratios with lower volcanic rates. A simple heat balance analysis suggests that the preponderance of volcanic systems must be open magmatic systems with respect to heat and matter transport in order to maintain eruptible magma at shallow depth throughout the observed lifetime of the volcano. The empirical upper limit of Å`10-2 km3/yr for magma eruption rate in systems with relatively high intrusive:extrusive ratios may be a consequence of the fundamental parameters

Tomographic location of potential melt-bearing phenocrysts in lunar glass spherules

International Nuclear Information System (INIS)

Ebel, D.S.; Fogel, R.A.; Rivers, M.L.

2005-01-01

magma is thought to derive from ∼ 400 km depth, the calculations imply a 4 km depth of graphite oxidation (and melt saturation in C-O volatiles) during ascent. We have imaged several hundred similar orange glass spherules, from sample 74220,764, using synchrotron x-ray computer-aided microtomography (XRCMT). Our goals: (1) locate similar phenocrysts containing melt inclusions; (2) analyze phenocrysts to understand the evolution of the magma; (3) analyze melt and fluid inclusions using EPMA and FTIR to obtain direct evidence of magmatic volatiles and pristine bulk compositions.

Behavior of volatiles in arc volcanism : geochemical and petrologic evidence from active volcanoes in Indonesia

NARCIS (Netherlands)

Hoog, J.C.M. de

2001-01-01

Large amounts of material are recycled along subduction zones by uprising magmas, of which volcanoes are the surface expression. This thesis focuses on the behavior of volatiles elements (S, Cl, H) during these recycling processes. The study area is the Indonesian arc system, which

Juvenile pumice and pyroclastic obsidian reveal the eruptive conditions necessary for the stability of Plinian eruption of rhyolitic magma

Science.gov (United States)

Giachetti, T.; Shea, T.; Gonnermann, H. M.; McCann, K. A.; Hoxsie, E. C.

2016-12-01

Significant explosive activity generally precedes or coexists with the large effusion of rhyolitic lava (e.g., Mono Craters; Medicine Lake Volcano; Newberry; Chaitén; Cordón Caulle). Such explosive-to-effusive transitions and, ultimately, cessation of activity are commonly explained by the overall waning magma chamber pressure accompanying magma withdrawal, albeit modulated by magma outgassing. The tephra deposits of such explosive-to-effusive eruptions record the character of the transition - abrupt or gradual - as well as potential changes in eruptive conditions, such as magma composition, volatiles content, mass discharge rate, conduit size, magma outgassing. Results will be presented from a detailed study of both the gas-rich (pumice) and gas-poor (obsidian) juvenile pyroclasts produced during the Plinian phase of the 1060 CE Glass Mountain eruption of Medicine Lake Volcano, California. In the proximal deposits, a multitude of pumice-rich sections separated by layers rich in dense clasts suggests a pulsatory behavior of the explosive phase. Density measurements on 2,600 pumices show that the intermediate, most voluminous deposits have a near constant median porosity of 65%. However, rapid increase in porosity to 75-80% is observed at both the bottom and the top of the fallout deposits, suggestive of rapid variations in magma degassing. In contrast, a water content of pyroclastic obsidians of approximately 0.6 wt% does remain constant throughout the eruption, suggesting that the pyroclastic obsidians degassed up to a constant pressure of a few megapascals. Numerical modeling of eruptive magma ascent and degassing is used to provide constraints on eruption conditions.

Volatility of components of saturated vapours of UCl4-CsCl and UCl4-LiCl molten mixtures

International Nuclear Information System (INIS)

Smirnov, M.V.; Kudyakov, V.Ya.; Salyulev, A.B.; Komarov, V.E.; Posokhin, Yu.V.; Afonichkin, V.K.

1979-01-01

The flow method has been used for measuring the volatility of the components from UCl 4 -CsCl and UCl 4 -LiCl melted mixtures containing 2.0, 5.0, 12.0, 25.0, 33.0, 50.0, 67.0, and 83.0 mol.% of UCl 4 within the temperature ranges of 903-1188 K and 740-1200 K, respectively. The chemical composition of saturated vapours above the melted salts has been determined. The melted mixtures in question exhibit negative deviation from ideal behaviour. Made was the conclusion about the presence in a vapour phase, along with monomeric UCl 4 , LiCl, CsCl and Li 2 Cl 2 , Cs 2 Cl 2 dimers of double compounds of the MeUCl 5 most probable composition. Their absolute contribution into a total pressure above the UCl 4 -CsCl melted mixtures is considerably smaller than above the UCl 4 -LiCl mixtures

Advancing dynamic and thermodynamic modelling of magma oceans

Science.gov (United States)

Bower, Dan; Wolf, Aaron; Sanan, Patrick; Tackley, Paul

2017-04-01

The techniques for modelling low melt-fraction dynamics in planetary interiors are well-established by supplementing the Stokes equations with Darcy's Law. But modelling high-melt fraction phenomena, relevant to the earliest phase of magma ocean cooling, necessitates parameterisations to capture the dynamics of turbulent flow that are otherwise unresolvable in numerical models. Furthermore, it requires knowledge about the material properties of both solid and melt mantle phases, the latter of which are poorly described by typical equations of state. To address these challenges, we present (1) a new interior evolution model that, in a single formulation, captures both solid and melt dynamics and hence charts the complete cooling trajectory of a planetary mantle, and (2) a physical and intuitive extension of a "Hard Sphere" liquid equation of state (EOS) to describe silicate melt properties for the pressure-temperature (P-T) range of Earth's mantle. Together, these two advancements provide a comprehensive and versatile modelling framework for probing the far-reaching consequences of magma ocean cooling and crystallisation for Earth and other rocky planets. The interior evolution model accounts for heat transfer by conduction, convection, latent heat, and gravitational separation. It uses the finite volume method to ensure energy conservation at each time-step and accesses advanced time integration algorithms by interfacing with PETSc. This ensures it accurately and efficiently computes the dynamics throughout the magma ocean, including within the ultra-thin thermal boundary layers (modelling capabilities. The thermodynamics of mantle melting are represented using a pseudo-one-component model, which retains the simplicity of a standard one-component model while introducing a finite temperature interval for melting (important for multi-component systems). Our new high P-T liquid EOS accurately captures the energetics and physical properties of the partially molten

Magma-poor vs. magma-rich continental rifting and breakup in the Labrador Sea

Science.gov (United States)

Gouiza, M.; Paton, D.

2017-12-01

Magma-poor and magma-rich rifted margins show distinct structural and stratigraphic geometries during the rift to breakup period. In magma-poor margins, crustal stretching is accommodated mainly by brittle faulting and the formation of wide rift basins shaped by numerous graben and half-graben structures. Continental breakup and oceanic crust accretion are often preceded by a localised phase of (hyper-) extension where the upper mantle is embrittled, serpentinized, and exhumed to the surface. In magma-rich margins, the rift basin is narrow and extension is accompanied by a large magmatic supply. Continental breakup and oceanic crust accretion is preceded by the emplacement of a thick volcanic crust juxtaposing and underplating a moderately thinned continental crust. Both magma-poor and magma-rich rifting occur in response to lithospheric extension but the driving forces and processes are believed to be different. In the former extension is assumed to be driven by plate boundary forces, while in the latter extension is supposed to be controlled by sublithospheric mantle dynamics. However, this view fails in explaining observations from many Atlantic conjugate margins where magma-poor and magma-rich segments alternate in a relatively abrupt fashion. This is the case of the Labrador margin where the northern segment shows major magmatic supply during most of the syn-rift phase which culminate in the emplacement of a thick volcanic crust in the transitional domain along with high density bodies underplating the thinned continental crust; while the southern segment is characterized mainly by brittle extension, mantle seprentinization and exhumation prior to continental breakup. In this work, we use seismic and potential field data to describe the crustal and structural architectures of the Labrador margin, and investigate the tectonic and mechanical processes of rifting that may have controlled the magmatic supply in the different segments of the margin.

Petrology and oxygen isotope geochemistry of the Pucon ignimbrite - Southern Andean volcanic zone, Chile: Implications for genesis of mafic ignimbrites

International Nuclear Information System (INIS)

McCurry, Michael; Schmidt, Keegan

2001-01-01

Although mafic components of dominantly intermediate to silicic ignimbrites are rather common, voluminous, dominantly mafic ignimbrites are rare (e.g., Smith, 1979; cf. Freundt and Schmincke, 1995). Volcan Villarrica, the most active composite volcano in South America, located in the Southern Andean Volcanic Zone (SAVZ, Lopez-Escobar and Moreno, 1994a), has produced two such ignimbrites, respectively the Lican and Pucon Ignimbrites, in the last 14,000 years (Clavero, 1996). The two ignimbrites are low-Si andesite and basaltic-andesite to low-Si andesite, respectively, the former about twice as voluminous as the later (10 and 5 km 3 ). Eruption of the ignimbrites produced calderas respectively 5 and 2 km in diameter (Moreno, 1995; Clavero, 1996). In addition to its mafic bulk composition, the Pucon Ignimbrite (PI) is also distinguished by numerous xenolithic fragments among and also within magmatic pyroclasts. Many of these are fragments of granitoid rocks. Volcan Villarrica has also produced numerous smaller mafic ignimbrites and pyroclastic surge deposits, as well as dominantly basaltic fallout and lava flows (Lopez-Escobar and Moreno, 1994; Moreno, 1995; Clavero, 1996; Hickey-Vargas et al., 1989; Tormey et al., 1991). Reasons for the unusual style of mafic explosive activity at Volcan Villarrica are unclear. Clavero (1996), based upon an exemplary thesis-study of the physical volcanology and petrology of the PI, suggests it formed in response to a sequence of events beginning with injection of a shallow basaltic andesite magma chamber by hotter basaltic magma. In his model mixing and heat transfer between the two magmas initiated a violent Strombolian eruption that destabilized the chamber causing infiltration of large amounts of meteoric-water saturated country rocks. The Pucon Ignimbrite formed in response to subsequent phreatomagmatic interactions. In contrast, Lopez-Escobar and Moreno (1994) infer on geochemical grounds that volatiles leading to the explosive

Rapid magma evolution constrained by zircon petrochronology and 40Ar/39Ar sanidine ages for the Huckleberry Ridge Tuff, Yellowstone, USA

DEFF Research Database (Denmark)

Rivera, Tiffany; Storey, Michael; Schmitz, Mark

2014-01-01

volcanic activity, zircon morphological zoning patterns coupled to strongly correlated changes in Ti-in-zircon thermometry and trace element indicators of progressive differentiation provide a proxy record for the evolution of the HRT member B magma body. Tandem in situ and isotope dilution U-Pb dating......Understanding the time scales of magmatic differentiation, storage, and eruption of large volume silicic magmas is a primary goal of igneous petrology. Within the Huckleberry Ridge Tuff (HRT; Idaho, USA), representing the earliest and largest caldera-forming eruption associated with Yellowstone...... differentiated over ~10 k.y. prior to eruption at 2.0794 ± 0.0046 Ma as defined by new astronomically calibrated, single-crystal total fusion 40Ar/39Ar sanidine analyses. This refined eruption age demonstrates that the transitional polarity preserved by HRT member B does not record the Reunion subchron...

Shallow magma diversions during explosive maar-diatreme eruptions in mafic volcanic fields

Science.gov (United States)

Le Corvec, N.; Muirhead, J.; White, J. D. L.

2017-12-01

Maar-diatremes are inverted conical structures formed by subterranean excavation and remobilization of country rocks during explosive volcanism and common in mafic volcanic fields. We focus on impacts of excavation and filling of maar-diatremes on the local state of stress, and its subsequent influence on underlying feeder dikes, which are critical for understanding the development of intrusive networks that feed surface eruptions. We address this issue using finite element models in COMSOL Multiphysics®. Inverted conical structures of varying sizes are excavated in a gravitationally loaded elastic half-space, and then progressively filled with volcaniclastic material, resulting in changes in the orientations and magnitudes of stresses generated within surrounding rocks and within the filling portion of the maar-diatreme. Our results show that rapid unloading during maar-diatreme excavation generates a horizontal compressive stress state beneath diatremes. These stresses allow magma to divert laterally as saucer-shaped sills and circumferential dikes at varying depths in the shallow feeder system, and produce intrusion geometries consistent with both field observations from exhumed volcanic fields and conceptual models of diatreme growth. Stresses generated in these models also provide an explanation for the evolving locations of fragmentation zones over the course of diatreme's filling. In particular, results from this study suggest that: (1) extensional stresses at the base of the diatreme fill favor magma ascent in the lower half of the structure, and possibly promote volatile exsolution and magma fragmentation; and (2) increased filling of diatremes creates a shallow compressive stress state that can inhibit magma ascent to the surface, promoting widespread intra-diatreme explosions, efficient mixing of host rock, and upward widening of the diatreme structure.

Attributes of the soil fertilized with sewage sludge and calcium and magnesium silicate

Directory of Open Access Journals (Sweden)

Geraldo R. Zuba Junio

2015-11-01

Full Text Available ABSTRACTThis study aimed to evaluate the chemical attributes of an Inceptisol cultivated with castor bean (Ricinus communis L., variety ‘BRS Energia’, fertilized with sewage sludge compost and calcium (Ca and magnesium (Mg silicate. The experiment was conducted at the ICA/UFMG, in a randomized block design, using a 2 x 4 factorial scheme with three replicates, and the treatments consisted of two doses of Ca-Mg silicate (0 and 1 t ha-1 and four doses of sewage sludge compost (0, 23.81, 47.62 and 71.43 t ha-1, on dry basis. Soil organic matter (OM, pH, sum of bases (SB, effective cation exchange capacity (CEC(t, total cation exchange capacity (CEC(T, base saturation (V% and potential acidity (H + Al were evaluated. There were no significant interactions between doses of sewage sludge compost and doses of Ca-Mg silicate on soil attributes, and no effect of silicate fertilization on these attributes. However, fertilization with sewage sludge compost promoted reduction in pH and increase in H + Al, OM and CEC. The dose of 71.43 t ha-1 of sewage sludge compost promoted the best soil chemical conditions.

Magma Mixing: Magmatic Enclaves in Morne Micotrin, Dominica

Science.gov (United States)

Hickernell, S.; Frey, H. M.; Manon, M. R. F.; Waters, L. E.

2017-12-01

Magmatic enclaves in volcanic rocks provide direct evidence of magma mingling/mixing within a magma reservoir and may reinvigorate the system and trigger eruption, as documented at the Soufriere Hills in Montserrat. Lava domes on the neighboring island of Dominica also contain multiple enclave populations and may be evidence for similar magma chamber processes. The central dome of Micotrin is at the head of the Roseau Valley, which was filled with 3 km3 of pyroclastic deposits from eruptions spanning 65 - 25 ka. There appear to be two distinct types of enclaves in the crystal-rich Micotrin andesites (60 wt% SiO2), fine-grained and coarse-grained. Fine-grained mafic enclaves (52 wt% SiO2) vary in size from 1 to 15 cm in diameter, whereas the coarse-grained enclaves are generally larger and range from 3-20 cm. Fine-grained enclaves are saturated in plag (35%) + opx (35%) + cpx (20%) + oxides (10%). Average pyroxenes are 0.01 to 0.02 cm in size, whereas plagioclase averages 0.05 cm and up to 0.1 cm. The texture of the fine-grained enclaves is cumulate-like, devoid of microlites and matrix glass. Coarse-grained enclaves lack cpx and have different modal abundances and textures: plag (75%) + opx (10%) + oxides (5%) + plag microlites (10%). Plagioclase are 0.1 cm in size and orthopyroxenes average 0.05 cm. The coarse-grained enclaves are highly vesicular, a notable difference from the host as well as the fine-grained enclaves. The boundaries of both the fine- and coarse-grained enclaves are quite sharp and distinct and there do not appear to be enclave minerals disaggregated in the host rock. Temperatures were determined by two oxides. The fine-grained enclaves had two populations of magnetite, yielding 847 + 21° and 920 + 17°C. The coarse-grained enclave was 890 + 42 °C, but the oxides were extensively exsolved. Plagioclase composition in both coarse and fine-grained samples was comparable, ranging from An50 to An80. Despite compositional similarity the textures of

Silicon isotopes in angrites and volatile loss in planetesimals

Science.gov (United States)

Moynier, Frédéric; Savage, Paul S.; Badro, James; Barrat, Jean-Alix

2014-01-01

Inner solar system bodies, including the Earth, Moon, and asteroids, are depleted in volatile elements relative to chondrites. Hypotheses for this volatile element depletion include incomplete condensation from the solar nebula and volatile loss during energetic impacts. These processes are expected to each produce characteristic stable isotope signatures. However, processes of planetary differentiation may also modify the isotopic composition of geochemical reservoirs. Angrites are rare meteorites that crystallized only a few million years after calcium–aluminum-rich inclusions and exhibit extreme depletions in volatile elements relative to chondrites, making them ideal samples with which to study volatile element depletion in the early solar system. Here we present high-precision Si isotope data that show angrites are enriched in the heavy isotopes of Si relative to chondritic meteorites by 50–100 ppm/amu. Silicon is sufficiently volatile such that it may be isotopically fractionated during incomplete condensation or evaporative mass loss, but theoretical calculations and experimental results also predict isotope fractionation under specific conditions of metal–silicate differentiation. We show that the Si isotope composition of angrites cannot be explained by any plausible core formation scenario, but rather reflects isotope fractionation during impact-induced evaporation. Our results indicate planetesimals initially formed from volatile-rich material and were subsequently depleted in volatile elements during accretion. PMID:25404309

The Dovyren Intrusive Complex (Southern Siberia, Russia): Insights into dynamics of an open magma chamber with implications for parental magma origin, composition, and Cu-Ni-PGE fertility

Science.gov (United States)

Ariskin, Alexey; Danyushevsky, Leonid; Nikolaev, Georgy; Kislov, Evgeny; Fiorentini, Marco; McNeill, Andrew; Kostitsyn, Yuri; Goemann, Karsten; Feig, Sandrin T.; Malyshev, Alexey

2018-03-01

The Dovyren Intrusive Complex (DIC, Northern Baikal region, 728 Ma) includes the layered dunite-troctolite-gabbronorite Yoko-Dovyren massif (YDM), associated mafic-ultramafic sills, and dykes of olivine-rich to olivine-free gabbronorite. Major rock types of the DIC are presented, including a diversity of olivine orthocumulates to olivine-plagioclase and gabbroic adcumulates, carbonate-contaminated ultramafics and Cu-Ni-PGE mineralisation. Detailed comparisons of complete cross-sections of the YDM in its centre and at the NE and SW margins demonstrate differences in the cumulate succession, mineral chemistry, and geochemical structure that likely reflect variations in parental magma compositions. Combining petrochemical reconstructions for most primitive rocks and calculations using the COMAGMAT-5 model, it is shown that the central and peripheral parts of the intrusion formed by olivine-laden parental magmas ranged in their temperatures by 100 °C, approximately from 1290 °C ( 11 wt% MgO, olivine Fo88) to 1190 °C ( 8 wt% MgO, olivine Fo86). Thermodynamic modelling suggests that the most primitive high-Mg magma was S-undersaturated, whereas its derivatives became S-saturated at T piles to generate poorly-mineralised plagiodunite. In the troctolite and gabbroic parts of the Dovyren chamber, sulphide immiscibility likely occurred at lower temperatures, producing Cu-rich sulphide precursors, which gave rise to the 'platinum group mineral' (PGM-containing) troctolite and low-mineralised PGE-rich anorthosite in the Main Reef. The geochemical structure of the YDM demonstrates C-shaped distributions of TiO2, K2O, P2O5, and incompatible trace elements, which are 3-5 fold depleted in the cumulate rocks from the inner horizons of the intrusion with respect to the relatively thin lower and upper contact zones. In addition, a marked misbalance between estimates of the average composition of the YDM and that of the proposed olivine-laden parental magmas is established. This

Magmatic Longevity Constrained by ID-TIMS U-Pb Dating of Zircon and Titanite

Science.gov (United States)

Szymanowski, D.; Wotzlaw, J. F.; Ellis, B. S.; Bachmann, O.; Von Quadt, A.

2016-12-01

Clues about the timescales and thermal conditions associated with the growth and evacuation of large silicic magma reservoirs are frequently drawn from radiometric dating, diffusion modelling, or thermomechanical modelling. A growing amount of petrological and geochronological evidence, supported by thermal modelling, suggests that many silicic magma reservoirs may exist for some 104-106 years in the form of high-crystallinity mushes at relatively low temperatures ( 700-750°C; [1-3]). Geochronological studies addressing this issue typically utilise the U-Pb system in zircon capable of recording extended periods of crystallisation, particularly in evolved calc-alkaline systems that spend most of their lifetime zircon-saturated. In this study, we integrate U-Pb dating of zircon and titanite to investigate the longevity of the magma reservoir that produced the Kneeling Nun Tuff, a 35 Ma, >900 km3 crystal-rich rhyolitic super-eruption from the Mogollon-Datil volcanic field in New Mexico (USA). High-precision ID-TIMS U-Pb dates of single crystals of both zircon and titanite independently record a continuous crystallisation history over >400,000 years. We combine the dating of both accessory phases with textural, major, trace element and isotopic studies of single crystals, placing tight constraints on the thermal conditions of magma accumulation and storage while recording differentiation and rejuvenation processes within the magma reservoir. The results suggest a protracted `cool' upper-crustal storage of magma prior to the Kneeling Nun Tuff eruption followed by a melting event which reduced the magma crystallinity and conditioned it for eruption. [1] Bachmann & Bergantz (2004), J. Petrol. 45, 1565-1582. [2] Gelman et al. (2013), Geology 41, 759-762. [3] Cooper & Kent (2014), Nature 506, 480-483.

Magma emplacement in 3D

Science.gov (United States)

Gorczyk, W.; Vogt, K.

2017-12-01

Magma intrusion is a major material transfer process in Earth's continental crust. Yet, the mechanical behavior of the intruding magma and its host are a matter of debate. In this study, we present a series of numerical thermo-mechanical experiments on mafic magma emplacement in 3D.In our model, we place the magmatic source region (40 km diameter) at the base of the mantle lithosphere and connect it to the crust by a 3 km wide channel, which may have evolved at early stages of magmatism during rapid ascent of hot magmatic fluids/melts. Our results demonstrate continental crustal response due to magma intrusion. We observe change in intrusion geometries between dikes, cone-sheets, sills, plutons, ponds, funnels, finger-shaped and stock-like intrusions as well as injection time. The rheology and temperature of the host-rock are the main controlling factors in the transition between these different modes of intrusion. Viscous deformation in the warm and deep crust favours host rock displacement and magma pools along the crust-mantle boundary forming deep-seated plutons or magma ponds in the lower to middle-crust. Brittle deformation in the cool and shallow crust induces cone-shaped fractures in the host rock and enables emplacement of finger- or stock-like intrusions at shallow or intermediate depth. A combination of viscous and brittle deformation forms funnel-shaped intrusions in the middle-crust. Low-density source magma results in T-shaped intrusions in cross-section with magma sheets at the surface.

Wear and chemistry of zirconium-silicate, aluminium-silicate and zirconium-aluminium-silicate glasses in alkaline medium

International Nuclear Information System (INIS)

Rouse, C.G.; Lemos Guenaga, C.M. de

1984-01-01

A study of the chemical durability, in alkaline solutions, of zirconium silicate, aluminium silicate, zirconium/aluminium silicate glasses as a function of glass composition is carried out. The glasses were tested using standard DIN-52322 method, where the glass samples are prepared in small polished pieces and attacked for 3 hours in a 800 ml solution of 1N (NaOH + NA 2 CO 3 ) at 97 0 C. The results show that the presence of ZrO 2 in the glass composition increases its chemical durability to alkaline attack. Glasses of the aluminium/zirconium silicate series were melted with and without TiO 2 . It was shown experimentally that for this series of glasses, the presence of both TiO 2 and ZrO 2 gave better chemical durability results. However, the best overall results were obtained from the simpler zirconium silicate glasses, where it was possible to make glasses with higher values of ZrO 2 . (Author) [pt

Indigenous abundances of siderophile elements in the lunar highlands: implications for the origin of the Moon

International Nuclear Information System (INIS)

Delano, J.W.; Ringwood, A.E.

1978-01-01

Substantial indigeneous abundances of siderophile elements have been found to be present in the lunar highlands. The abundances of 13 siderophile elements in the parental magma were estimated by using a simple model. It is shown that metal/silicate fractionation within the Moon cannot have been the cause of the siderophile element abundances in the parental highlands magma and primitive, low-Ti mare basalts. The relative abundances of the indigenous siderophile elements in highlands and mare samples seem, instead, to be the result of complex processes which operated prior to the Moon's accretion. The abundances of the relatively involatile, siderophile elements in the parental highlands magma are strikingly similar to the abundances observed in terrestrial oceanic tholeiites. Furthermore, the abundances of the relatively volatile, siderophile elements in the parental highlands magma are also systematically related to the corresponding abundances in terrestrial oceanic tholeiites. In fact, the parental magma of the lunar highlands can be essentially regarded as having been a volatile-depleted terrestrial oceanic tholeite. The origin of the moon is discussed in the context of the results. The probability that depletion of siderophile elements occurred in an earlier generation of differentiated planetesimals similar to those which formed the basaltic achondrites, stony-irons, and irons is examined but can be dismissed on several grounds. It seems that the uniquely terrestrial 'siderophile signature' within the Moon can be explained only if the Moon was derived from the Earth's mantle subsequent to core-formation. (Auth.)

Fault-Magma Interactions during Early Continental Rifting: Seismicity of the Magadi-Natron-Manyara basins, Africa

Science.gov (United States)

Weinstein, A.; Oliva, S. J.; Ebinger, C.; Aman, M.; Lambert, C.; Roecker, S. W.; Tiberi, C.; Muirhead, J.

2017-12-01

Although magmatism may occur during the earliest stages of continental rifting, its role in strain accommodation remains weakly constrained by largely 2D studies. We analyze seismicity data from a 13-month, 39-station broadband seismic array to determine the role of magma intrusion on state-of-stress and strain localization, and their along-strike variations. Precise earthquake locations using cluster analyses and a new 3D velocity model reveal lower crustal earthquakes along projections of steep border faults that degas CO2. Seismicity forms several disks interpreted as sills at 6-10 km below a monogenetic cone field. The sills overlie a lower crustal magma chamber that may feed eruptions at Oldoinyo Lengai volcano. After determining a new ML scaling relation, we determine a b-value of 0.87 ± 0.03. Focal mechanisms for 66 earthquakes, and a longer time period of relocated earthquakes from global arrays reveal an along-axis stress rotation of 50 o ( N150 oE) in the magmatically active zone. Using Kostrov summation of local and teleseismic mechanisms, we find opening directions of N122ºE and N92ºE north and south of the magmatically active zone. The stress rotation facilitates strain transfer from border fault systems, the locus of early stage deformation, to the zone of magma intrusion in the central rift. Our seismic, structural, and geochemistry results indicate that frequent lower crustal earthquakes are promoted by elevated pore pressures from volatile degassing along border faults, and hydraulic fracture around the margins of magma bodies. Earthquakes are largely driven by stress state around inflating magma bodies, and more dike intrusions with surface faulting, eruptions, and earthquakes are expected.

DETERMINATION OF SATURATION VAPOR PRESSURE OF LOW VOLATILE SUBSTANCES THROUGH THE STUDY OF EVAPORATION RATE BY THERMOGRAVIMETRIC ANALYSIS

Directory of Open Access Journals (Sweden)

R. V. Ralys

2015-11-01

Full Text Available Subject of Study.Research of vapor pressure of low volatile substances is a complicated problem due to both direct experimental implementation complexity and, most significantly, the issues faced correctness of the analysis and processing of experimental data. That is why it is usually required engaging the reference substances (with vapor pressures well studied. The latter drastically reduces the effectiveness of the experimental methods used and narrows their applicability. The paper deals with an approach to the evaporation process description (sublimation of low volatile substances based on molecular kinetic description in view of diffusive and convection processes. The proposed approach relies on experimental thermogravimetricfindingsina wide range of temperatures, flow rates ofthe purge gas and time. Method. A new approach is based on the calculation of the vapor pressure and uses the data about the speed of evaporation by thermogravimetric analysis depending on the temperature, the flow rate of the purge gas, and the evaporation time. The basis for calculation is the diffusion-kinetic description of the process of evaporation (mass loss of the substance from the exposed surface. The method is applicable to determine the thermodynamic characteristics for both the evaporation (the equilibrium liquid - vapor and sublimation (the equilibrium solid - vapor. We proposed the appropriate method of the experiment and analysis of its data in order to find the saturated vapor pressure of individual substances of low volatility. Main Results. The method has been tested on substances with insufficiently reliable and complete study of the thermodynamic characteristics but, despite this, are often used (because of the other data limitations as reference ones. The vaporization process (liquid-vapor has been studied for di-n-butyl phthalate C16H22O4 at 323,15–443,15 К, and sublimation for benzoic acid C7H6O2at 303,15–183,15 К. Both processes have

Sunset Crater, AZ: Evolution of a highly explosive basaltic eruption as indicated by granulometry and clast componentry

Science.gov (United States)

Allison, C. M.; Clarke, A. B.; Pioli, L.; Alfano, F.

2011-12-01

Basaltic scoria cone volcanoes are the most abundant volcanic edifice on Earth and occur in all tectonic settings. Basaltic magmas have lower viscosities, higher temperatures, and lower volatile contents than silicic magmas, and therefore generally have a lower potential for explosive activity. However, basaltic eruptions display great variability in eruptive style, from mild lava flows to more energetic explosions with large plumes. The San Francisco Volcanic Field (SFVF) in northern Arizona, active from 6 Ma-present, consists of over 600 volcanoes, mostly alkali basalt scoria cones, and five silicic centers [Wood and Kienle (1990), Cambridge University Press]. The eruption of Sunset Crater in the SFVF during the Holocene was an anomalously large basaltic explosive eruption, consisting of eight tephra-bearing phases and three lava flows [Amos (1986), MS thesis, ASU]. Typical scoria cone-forming eruptions have volumes sorted. Future work will include textural analysis of bubbles and crystals to understand the ascent and cooling history of the different clast types, and also to better interpret differences in abundance as related to variations in eruption or vent dynamics.

Retrogressive hydration of calc-silicate xenoliths in the eastern Bushveld complex: evidence for late magmatic fluid movement

Science.gov (United States)

Wallmach, T.; Hatton, C. J.; De Waal, S. A.; Gibson, R. L.

1995-11-01

Two calc-silicate xenoliths in the Upper Zone of the Bushveld complex contain mineral assemblages which permit delineation of the metamorphic path followed after incorporation of the xenoliths into the magma. Peak metamorphism in these xenoliths occurred at T=1100-1200°C and P <1.5 kbar. Retrograde metamorphism, probably coinciding with the late magmatic stage, is characterized by the breakdown of akermanite to monticellite and wollastonite at 700°C and the growth of vesuvianite from melilite. The latter implies that water-rich fluids (X CO 2 <0.2) were present and probably circulating through the cooling magmatic pile. In contrast, calc-silicate xenoliths within the lower zones of the Bushveld complex, namely in the Marginal and Critical Zones, also contain melilite, monticellite and additional periclase with only rare development of vesuvianite. This suggests that the Upper Zone cumulate pile was much 'wetter' in the late-magmatic stage than the earlier-formed Critical and Marginal Zone cumulate piles.

Eruption Depths, Magma Storage and Magma Degassing at Sumisu Caldera, Izu-Bonin Arc: Evidence from Glasses and Melt Inclusions

Science.gov (United States)

Johnson, E. R.

2015-12-01

Island arc volcanoes can become submarine during cataclysmal caldera collapse. The passage of a volcanic vent from atmospheric to under water environment involves complex modifications of the eruption style and subsequent transport of the pyroclasts. Here, we use FTIR measurements of the volatile contents of glass and melt inclusions in the juvenile pumice clasts in the Sumisu basin and its surroundings (Izu-Bonin arc) to investigate changes in eruption depths, magma storage and degassing over time. This study is based on legacy cores from ODP 126, where numerous unconsolidated (250 m), massive to normally graded pumice lapilli-tuffs were recovered over four cores (788C, 790A, 790B and 791A). Glass and clast geochemistry indicate the submarine Sumisu caldera as the source of several of these pumice lapilli-tuffs. Glass chips and melt inclusions from these samples were analyzed using FTIR for H2O and CO2 contents. Glass chips record variable H2O contents; most chips contain 0.6-1.6 wt% H2O, corresponding to eruption depths of 320-2100 mbsl. Variations in glass H2O and pressure estimates suggest that edifice collapse occurred prior-to or during eruption of the oldest of these samples, and that the edifice may have subsequently grown over time. Sanidine-hosted melt inclusions from two units record variably degassed but H2O-rich melts (1.1-5.6 wt% H2O). The lowest H2O contents overlap with glass chips, consistent with degassing and crystallization of melts until eruption, and the highest H2O contents suggest that large amounts of degassing accompanied likely explosive eruptions. Most inclusions, from both units, contain 2-4 wt% H2O, which further indicates that the magmas crystallized at pressures of ~50-100 MPa, or depths ~400-2800 m below the seafloor. Further glass and melt inclusion analyses, including major element compositions, will elucidate changes in magma storage, degassing and evolution over time.

The role of magma mixing/mingling and cumulate melting in the Neapolitan Yellow Tuff caldera-forming eruption (Campi Flegrei, Southern Italy)

Science.gov (United States)

Forni, Francesca; Petricca, Eleonora; Bachmann, Olivier; Mollo, Silvio; De Astis, Gianfilippo; Piochi, Monica

2018-06-01

Understanding the mechanisms responsible for the generation of chemical gradients in high-volume ignimbrites is key to retrieve information on the processes that control the maturation and eruption of large silicic magmatic reservoirs. Over the last 60 ky, two large ignimbrites showing remarkable zoning were emplaced during caldera-forming eruptions at Campi Flegrei (i.e., Campanian Ignimbrite, CI, 39 ka and Neapolitan Yellow Tuff, NYT, 15 ka). While the CI displays linear compositional, thermal and crystallinity gradients, the NYT is a more complex ignimbrite characterized by crystal-poor magmas ranging in composition from trachy-andesites to phonolites. By combining major and trace element compositions of matrix glasses and mineral phases from juvenile clasts located at different stratigraphic heights along the NYT pyroclastic sequence, we interpret such compositional gradients as the result of mixing/mingling between three different magmas: (1) a resident evolved magma showing geochemical characteristics of a melt extracted from a cumulate mush dominated by clinopyroxene, plagioclase and oxides with minor sanidine and biotite; (2) a hotter and more mafic magma from recharge providing high-An plagioclase and high-Mg clinopyroxene crystals and (3) a compositionally intermediate magma derived from remelting of low temperature mineral phases (i.e., sanidine and biotite) within the cumulate crystal mush. We suggest that the presence of a refractory crystal mush, as documented by the occurrence of abundant crystal clots containing clinopyroxene, plagioclase and oxides, is the main reason for the lack of erupted crystal-rich material in the NYT. A comparison between the NYT and the CI, characterized by both crystal-poor extracted melts and crystal-rich magmas representing remobilized portions of a "mature" (i.e., sanidine dominated) cumulate residue, allows evaluation of the capability of crystal mushes of becoming eruptible upon recharge.

The permeability evolution of tuffisites and outgassing from dense rhyolitic magma

Science.gov (United States)

Heap, M. J.; Tuffen, H.; Wadsworth, F. B.; Reuschlé, T.; Castro, J. M.; Schipper, C. I.

2017-12-01

Recent observations of rhyolitic lava effusion from eruptions in Chile indicate that simultaneous pyroclastic venting facilitates outgassing. Venting from conduit-plugging lava domes is pulsatory and occurs through shallow fracture networks that deliver pyroclastic debris and exsolved gases to the surface. However, these fractures become blocked as the particulate fracture infill sinters viscously, thus drastically reducing permeability. Tuffisites, fossilized debris-filled fractures of this venting process, are abundant in pyroclastic material ejected during hybrid explosive-effusive activity. Dense tuffisite-hosting obsidian bombs ejected from Volcán Chaitén (Chile) in 2008 afford an opportunity to better understand the permeability evolution of tuffisites within low-permeability conduit plugs, wherein gas mobility is reliant upon fracture pathways. We use laboratory measurements of the permeability and porosity of tuffisites that preserve different degrees of sintering, combined with a grainsize-based sintering model and constraints on pressure-time paths from H2O diffusion, to place first-order constraints on tuffisite permeability evolution. Inferred timescales of sintering-driven tuffisite compaction and permeability loss, spanning minutes to hours, coincide with observed vent pulsations during hybrid rhyolitic activity and, more broadly, timescales of pressurization accompanying silicic lava dome extrusion. We therefore conclude that sintering exerts a first-order control on fracture-assisted outgassing from low-permeability, conduit-plugging silicic magma.

Disclosing Multiple Magma Degassing Sources Offers Unique Insights of What's Behind the Campi Flegrei Caldera Unrest

Science.gov (United States)

Moretti, R.; Civetta, L.; Orsi, G.; Arienzo, I.; D'Antonio, M.; Di Renzo, V.

2013-12-01

The definition of the structure and evolution of the magmatic system of Campi Flegrei caldera (CFc), Southern Italy, has been a fundamental tool for the assessment of the short-term volcanic hazard. The ensemble of geophysical and petrologic data show that the CFc magmatic system has been -and still is- characterized by two major reservoirs at different depths. From the deep one (around 8 km), less evolved magmas crystallize and degas, supplying fluids and magmas to the shallow (3-4 km) reservoirs. A thorough reconstruction of processes occurring in magma chamber/s prior and/or during the CFc eruptions has shown that magmas entering shallow reservoirs mixed with resident and crystallized batches. Also the 1982-85 unrest episode has been related to a magma intrusion of 2.1 x 10^7 m^3 at 3-4 km depth, on the basis of geophysical data (ground deformation, gravimetry, seismic imaging) and their interpretation. Thermodynamic evaluation of magma properties, at the time of emplacement, suggests for such an intrusion a bulk density of 2.000 kg/m^3 . Such a value testifies the high amount of exsolved volatiles within the system. The available record of geochemical and isotopic data on surface fumaroles, coupled with melt inclusion data, has already shown that dual (deep and shallow) magma degassing from such two reservoirs, as well as their interaction with the hydrothermal system, allows explaining the relevant fluctuations observed at crater fumaroles after the 1982-85 magma intrusion. An important role was played by the rapid crystallization (around 30 years) of the shallow magma, such that in the recent years gas discharges should be fuelled mostly by the deep magma. Such a process is well recorded in the fumarolic gas composition of the last ~10 years, but has to be reconciled with the unrest dynamics which took place after year 2000, characterized by a slow but continuous ground uplift. All geochemical indicators (major species and noble gases) point to three possible

Magma evolution inside the 1631 Vesuvius magma chamber and eruption triggering

Directory of Open Access Journals (Sweden)

Stoppa Francesco

2017-03-01

Full Text Available Vesuvius is a high-risk volcano and the 1631 Plinian eruption is a reference event for the next episode of explosive unrest. A complete stratigraphic and petrographic description of 1631 pyroclastics is given in this study. During the 1631 eruption a phonolite was firstly erupted followed by a tephritic phonolite and finally a phonolitic tephrite, indicating a layered magma chamber. We suggest that phonolitic basanite is a good candidate to be the primitive parental-melt of the 1631 eruption. Composition of apatite from the 1631 pyroclastics is different from those of CO2-rich melts indicating negligible CO2 content during magma evolution. Cross checking calculations, using PETROGRAPH and PELE software, accounts for multistage evolution up to phonolite starting from a phonolitic basanite melt similar to the Vesuvius medieval lavas. The model implies crystal settling of clinopyroxene and olivine at 6 kbar and 1220°C, clinopyroxene plus leucite at a pressure ranging from 2.5 to 0.5 kbar and temperature ranging from 1140 to 940°C. Inside the phonolitic magma chamber K-feldspar and leucite would coexist at a temperature ranging from from 940 to 840°C and at a pressure ranging from 2.5 to0.5 kbar. Thus crystal fractionation is certainly a necessary and probably a sufficient condition to evolve the melt from phono tephritic to phonolitic in the 1631 magma chamber. We speculate that phonolitic tephrite magma refilling from deeper levels destabilised the chamber and triggered the eruption, as testified by the seismic precursor phenomena before 1631 unrest.

Magma evolution inside the 1631 Vesuvius magma chamber and eruption triggering

Science.gov (United States)

Stoppa, Francesco; Principe, Claudia; Schiazza, Mariangela; Liu, Yu; Giosa, Paola; Crocetti, Sergio

2017-03-01

Vesuvius is a high-risk volcano and the 1631 Plinian eruption is a reference event for the next episode of explosive unrest. A complete stratigraphic and petrographic description of 1631 pyroclastics is given in this study. During the 1631 eruption a phonolite was firstly erupted followed by a tephritic phonolite and finally a phonolitic tephrite, indicating a layered magma chamber. We suggest that phonolitic basanite is a good candidate to be the primitive parental-melt of the 1631 eruption. Composition of apatite from the 1631 pyroclastics is different from those of CO2-rich melts indicating negligible CO2 content during magma evolution. Cross checking calculations, using PETROGRAPH and PELE software, accounts for multistage evolution up to phonolite starting from a phonolitic basanite melt similar to the Vesuvius medieval lavas. The model implies crystal settling of clinopyroxene and olivine at 6 kbar and 1220°C, clinopyroxene plus leucite at a pressure ranging from 2.5 to 0.5 kbar and temperature ranging from 1140 to 940°C. Inside the phonolitic magma chamber K-feldspar and leucite would coexist at a temperature ranging from from 940 to 840°C and at a pressure ranging from 2.5 to0.5 kbar. Thus crystal fractionation is certainly a necessary and probably a sufficient condition to evolve the melt from phono tephritic to phonolitic in the 1631 magma chamber. We speculate that phonolitic tephrite magma refilling from deeper levels destabilised the chamber and triggered the eruption, as testified by the seismic precursor phenomena before 1631 unrest.

Thermal History and Volatile Partitioning between Proto-Atmosphere and Interior of Mars Accreted in a Solar Nebula

Science.gov (United States)

Saito, Hiroaki; Kuramoto, Kiyoshi

2015-11-01

Recent precise Hf-W chronometry of Martian meteorites reveals that Mars had likely reached the half of its present mass within 3 Myr from the birth of the solar system (Dauphas and Pourmand, 2011). Hence, the accretion is considered to almost proceed within the solar nebula associated with the capture of nebula gas components. At the same time, the impact degassing may inevitably occur because impact velocity increases high enough for such degassing when a proto-planet gets larger than around lunar size. Thus, we can expect the formation of a hybrid-type proto-atmosphere that consists of nebula gas and degassed one.This study analyzes the thermal structure of this proto-atmosphere sustained by accretional heating by building a 1D radiative-convective equilibrium model. Raw materials of Mars are supposed to be volatile-rich on the basis of the geochemical systematics of Mars meteorites (Dreibus and Wanke, 1988). The composition of degassed component comprised of H2, H2O, CH4, and CO is determined by chemical equilibrium with silicate and metal under the physical condition of locally heated region generated by each impact (Kuramoto, 1997). Degassed component lies beneath the nebula gas atmosphere at altitudes below the compositional boundary height that would change depending on the amount of degassed component. The accretion time is taken to be from 1 to 6 Myr.Our model predicts that the surface temperature exceeds the liquidus temperature of rock when a proto Mars grows larger than 0.7 times of its present mass for the longest accretion time case. In this case, the magma ocean mass just after the end of accretion is 0.2 times of its present mass if heat transfer and heat sources such as short-lived radionuclides are neglected in the interior. The corresponding amount of water dissolved into the magma ocean would be around 1.8 times the present Earth ocean mass. These results suggest that the earliest Mars would be hot enough to form deep magma oceans, which

Re-appraisal of the Magma-rich versus Magma-poor Paradigm at Rifted Margins: consequences for breakup processes

Science.gov (United States)

Tugend, J.; Gillard, M.; Manatschal, G.; Nirrengarten, M.; Harkin, C. J.; Epin, M. E.; Sauter, D.; Autin, J.; Kusznir, N. J.; McDermott, K.

2017-12-01

Rifted margins are often classified based on their magmatic budget only. Magma-rich margins are commonly considered to have excess decompression melting at lithospheric breakup compared with steady state seafloor spreading while magma-poor margins have suppressed melting. New observations derived from high quality geophysical data sets and drill-hole data have revealed the diversity of rifted margin architecture and variable distribution of magmatism. Recent studies suggest, however, that rifted margins have more complex and polyphase tectono-magmatic evolutions than previously assumed and cannot be characterized based on the observed volume of magma alone. We compare the magmatic budget related to lithospheric breakup along two high-resolution long-offset deep reflection seismic profiles across the SE-Indian (magma-poor) and Uruguayan (magma-rich) rifted margins. Resolving the volume of magmatic additions is difficult. Interpretations are non-unique and several of them appear plausible for each case involving variable magmatic volumes and mechanisms to achieve lithospheric breakup. A supposedly 'magma-poor' rifted margin (SE-India) may show a 'magma-rich' lithospheric breakup whereas a 'magma-rich' rifted margin (Uruguay) does not necessarily show excess magmatism at lithospheric breakup compared with steady-state seafloor spreading. This questions the paradigm that rifted margins can be subdivided in either magma-poor or magma-rich margins. The Uruguayan and other magma-rich rifted margins appear characterized by an early onset of decompression melting relative to crustal breakup. For the converse, where the onset of decompression melting is late compared with the timing of crustal breakup, mantle exhumation can occur (e.g. SE-India). Our work highlights the difficulty in determining a magmatic budget at rifted margins based on seismic reflection data alone, showing the limitations of margin classification based solely on magmatic volumes. The timing of

Why Is There an Abrupt Transition from Solid Rock to Low Crystallinity Magma in Drilled Magma Bodies?

Science.gov (United States)

Eichelberger, J. C.; Carrigan, C. R.; Sun, Y.; Lavallée, Y.

2017-12-01

We report on a preliminary evaluation, from basic principles of heat and mass transfer, on the unexpectedly abrupt transition from cuttings of solid rock to fragments of crystal poor glass during drilling into magma bodies. Our analysis is based on conditions determined and inferred for the 2009 IDDP-1 well in Krafla Caldera, which entered apparently liquidus rhyolite magma at about 900oC at a depth of 2104 m. Simple conduction would predict some 30 m of crystallization and partial crystallization since the latest time the magma could have been intruded, approximately 30 years prior to discovery by drilling. Option 1: The expected crystallization of magma has occurred but interstitial melt remains. The pressure difference between lithostatic load of about 50 MPa on the mush and 20 MPa hydrostatic pressure in the well causes pore melt to flow from the permeable mush into the borehole, where it becomes the source of the quenched melt chips. To be viable, this mechanism must work over the time frame of a day. Option 2: The expected crystallization is occurring, but high Rayleigh number thermal convection in the magma chamber continuously displaces crystallizing roof magma by liquidus magma from the interior of the body. To be viable, this mechanism must result in overturning magma in the chamber on a time scale that is much shorter than that of crystallization. Option 3: Flow-induced crystal migration away from zones of high shear created during drilling into magma may preferentially produce low-crystal-content melt at the boundary of the borehole, which is then sampled.

Linking rapid magma reservoir assembly and eruption trigger mechanisms at evolved Yellowstone-type supervolcanoes

Science.gov (United States)

Wotzlaw, J.F.; Bindeman, I.N.; Watts, Kathryn E.; Schmitt, A.K.; Caricchi, L.; Schaltegger, U.

2014-01-01

The geological record contains evidence of volcanic eruptions that were as much as two orders of magnitude larger than the most voluminous eruption experienced by modern civilizations, the A.D. 1815 Tambora (Indonesia) eruption. Perhaps nowhere on Earth are deposits of such supereruptions more prominent than in the Snake River Plain–Yellowstone Plateau (SRP-YP) volcanic province (northwest United States). While magmatic activity at Yellowstone is still ongoing, the Heise volcanic field in eastern Idaho represents the youngest complete caldera cycle in the SRP-YP, and thus is particularly instructive for current and future volcanic activity at Yellowstone. The Heise caldera cycle culminated 4.5 Ma ago in the eruption of the ∼1800 km3 Kilgore Tuff. Accessory zircons in the Kilgore Tuff display significant intercrystalline and intracrystalline oxygen isotopic heterogeneity, and the vast majority are 18O depleted. This suggests that zircons crystallized from isotopically distinct magma batches that were generated by remelting of subcaldera silicic rocks previously altered by low-δ18O meteoric-hydrothermal fluids. Prior to eruption these magma batches were assembled and homogenized into a single voluminous reservoir. U-Pb geochronology of isotopically diverse zircons using chemical abrasion–isotope dilution–thermal ionization mass spectrometry yielded indistinguishable crystallization ages with a weighted mean 206Pb/238U date of 4.4876 ± 0.0023 Ma (MSWD = 1.5; n = 24). These zircon crystallization ages are also indistinguishable from the sanidine 40Ar/39Ar dates, and thus zircons crystallized close to eruption. This requires that shallow crustal melting, assembly of isolated batches into a supervolcanic magma reservoir, homogenization, and eruption occurred extremely rapidly, within the resolution of our geochronology (103–104 yr). The crystal-scale image of the reservoir configuration, with several isolated magma batches, is very similar to the

Experimental simulation of magma-carbonate interaction beneath Mt. Vesuvius, Italy

Science.gov (United States)

Jolis, E. M.; Freda, C.; Troll, V. R.; Deegan, F. M.; Blythe, L. S.; McLeod, C. L.; Davidson, J. P.

2013-11-01

We simulated the process of magma-carbonate interaction beneath Mt. Vesuvius in short duration piston-cylinder experiments under controlled magmatic conditions (from 0 to 300 s at 0.5 GPa and 1,200 °C), using a Vesuvius shoshonite composition and upper crustal limestone and dolostone as starting materials. Backscattered electron images and chemical analysis (major and trace elements and Sr isotopes) of sequential experimental products allow us to identify the textural and chemical evolution of carbonated products during the assimilation process. We demonstrate that melt-carbonate interaction can be extremely fast (minutes), and results in dynamic contamination of the host melt with respect to Ca, Mg and 87Sr/86Sr, coupled with intense CO2 vesiculation at the melt-carbonate interface. Binary mixing between carbonate and uncontaminated melt cannot explain the geochemical variations of the experimental charges in full and convection and diffusion likely also operated in the charges. Physical mixing and mingling driven by exsolving volatiles seems to be a key process to promote melt homogenisation. Our results reinforce hypotheses that magma-carbonate interaction is a relevant and ongoing process at Mt. Vesuvius and one that may operate not only on a geological, but on a human timescale.

Magma flow through elastic-walled dikes

NARCIS (Netherlands)

Bokhove, Onno; Woods, A.W.; de Boer, A

2005-01-01

A convection–diffusion model for the averaged flow of a viscous, incompressible magma through an elastic medium is considered. The magma flows through a dike from a magma reservoir to the Earth’s surface; only changes in dike width and velocity over large vertical length scales relative to the

Fault-magma interactions during early continental rifting: Seismicity of the Magadi-Natron-Manyara basins, Africa

Science.gov (United States)

Weinstein, A.; Oliva, S. J.; Ebinger, C. J.; Roecker, S.; Tiberi, C.; Aman, M.; Lambert, C.; Witkin, E.; Albaric, J.; Gautier, S.; Peyrat, S.; Muirhead, J. D.; Muzuka, A. N. N.; Mulibo, G.; Kianji, G.; Ferdinand-Wambura, R.; Msabi, M.; Rodzianko, A.; Hadfield, R.; Illsley-Kemp, F.; Fischer, T. P.

2017-10-01

Although magmatism may occur during the earliest stages of continental rifting, its role in strain accommodation remains weakly constrained by largely 2-D studies. We analyze seismicity data from a 13 month, 39-station broadband seismic array to determine the role of magma intrusion on state-of-stress and strain localization, and their along-strike variations. Precise earthquake locations using cluster analyses and a new 3-D velocity model reveal lower crustal earthquakes beneath the central basins and along projections of steep border faults that degas CO2. Seismicity forms several disks interpreted as sills at 6-10 km below a monogenetic cone field. The sills overlie a lower crustal magma chamber that may feed eruptions at Oldoinyo Lengai volcano. After determining a new ML scaling relation, we determine a b-value of 0.87 ± 0.03. Focal mechanisms for 65 earthquakes, and 13 from a catalogue prior to our array reveal an along-axis stress rotation of ˜60° in the magmatically active zone. New and prior mechanisms show predominantly normal slip along steep nodal planes, with extension directions ˜N90°E north and south of an active volcanic chain consistent with geodetic data, and ˜N150°E in the volcanic chain. The stress rotation facilitates strain transfer from border fault systems, the locus of early-stage deformation, to the zone of magma intrusion in the central rift. Our seismic, structural, and geochemistry results indicate that frequent lower crustal earthquakes are promoted by elevated pore pressures from volatile degassing along border faults, and hydraulic fracture around the margins of magma bodies. Results indicate that earthquakes are largely driven by stress state around inflating magma bodies.

Effect Of Intraruminal Infussion Of Saturated And Unsaturated Fatty ...

African Journals Online (AJOL)

This study describes the effect of intraruminal infusion of diferent proportions of palmitic (saturated fatty acid) and linolenic (unsaturated fatty acid) on rumen degradability of organic matter fraction of Pennisetium purpureum, total volatile fatty acid and total methane productions in West African Dwarf sheep. Five combination ...

Caldera resurgence driven by magma viscosity contrasts.

Science.gov (United States)

Galetto, Federico; Acocella, Valerio; Caricchi, Luca

2017-11-24

Calderas are impressive volcanic depressions commonly produced by major eruptions. Equally impressive is the uplift of the caldera floor that may follow, dubbed caldera resurgence, resulting from magma accumulation and accompanied by minor eruptions. Why magma accumulates, driving resurgence instead of feeding large eruptions, is one of the least understood processes in volcanology. Here we use thermal and experimental models to define the conditions promoting resurgence. Thermal modelling suggests that a magma reservoir develops a growing transition zone with relatively low viscosity contrast with respect to any newly injected magma. Experiments show that this viscosity contrast provides a rheological barrier, impeding the propagation through dikes of the new injected magma, which stagnates and promotes resurgence. In explaining resurgence and its related features, we provide the theoretical background to account for the transition from magma eruption to accumulation, which is essential not only to develop resurgence, but also large magma reservoirs.

Formation of anorthosite on the Moon through magma ocean fractional crystallization

Directory of Open Access Journals (Sweden)

Tatsuyuki Arai

2017-03-01

melt. One of the differences between the Earth and the Moon is the presence of water. If the terrestrial magma ocean was saturated with H2O, plagioclase could not crystallize, and anorthosite could not form.

Volatile-rich komatiitic and picritic melt inclusions in Cr-spinel beach sand from Gorgona Island, Colombia

Science.gov (United States)

Shimizu, K.; Shimizu, N.; Suzuki, K.; Tatsumi, Y.; Komiya, T.; Maruyama, S.

2007-12-01

Volatile content of komatiite is a key to constrain thermal evolution of the deep Earth. We report volatile contents with major and trace element compositions of melt inclusions (MIs) in chromian spinel (Cr-spinel) from beach sands of Gorgona Island, Colombia. Gorgona Island is ~90 Ma volcanic island, where picrites and the world-youngest komatiites occur. As Cr-spinel is dense and rigid oxide mineral that crystallizes only at early stages of crystallization, it is considered to be a superior container for retaining primitive melt, even including volatiles. Volatile (H2O, CO2, S, F and Cl) and trace element (K2O, Sr, Y, Zr, Nb, Ba, La, Ce, Sm, Dy, Yb) compositions of ~80 MIs were analyzed by SIMS (Cameca-1280 and 3f, respectively) at WHOI. MIs in the Cr-spinel from Gorgona Is. are classified into three types by their host Cr-spinel compositions such as low-Ti (P-type), high-Ti with high-Cr# (BK-type) and high-Ti with low-Cr# (K-type). MIs of P-type, BK-type and K-type are mostly in compositional ranges of picrite, high TiO2 komatiite (some basalt) and low TiO2 komatiite in Gorgona Island, respectively. Water content of P-type MIs is variable, ranging from 0.05 to 0.9 wt%, whereas those of BK and K-type MIs are limited (500 ppm) do not contain (shrinkage) bubbles and many of them are low in K2O. H2O/K2O, CO2/K2O, S/K2O and F/K2O ratios are positively correlated with Y/Sr ratios, indicating degassing trends of melt at crystallization, magma mixing and/or assimilation. Undegassed H2O/K2O, CO2/K2O, S/K2O and F/K2O ratios of komatiitic (picritic) melt are estimated to be ~10 (~40), ~80 (n.d.), ~7(~3) and ~1(~0.5), respectively, which are much higher than those estimated for the depleted source mantle of the MORB [1.6, 0.7, 1.6 and 0.2, respectively; Salters, V. & Stracke, A. (2004), Composition of the depleted mantle. Geochem. Geophys. Geosys. 5 (2003GC000597)]. The results suggest that Gorgona komatiite and picrite magmas were derived from volatile-rich sources. CO2

Time-resolved seismic tomography detects magma intrusions at Mount Etna.

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Patanè, D; Barberi, G; Cocina, O; De Gori, P; Chiarabba, C

2006-08-11

The continuous volcanic and seismic activity at Mount Etna makes this volcano an important laboratory for seismological and geophysical studies. We used repeated three-dimensional tomography to detect variations in elastic parameters during different volcanic cycles, before and during the October 2002-January 2003 flank eruption. Well-defined anomalous low P- to S-wave velocity ratio volumes were revealed. Absent during the pre-eruptive period, the anomalies trace the intrusion of volatile-rich (>/=4 weight percent) basaltic magma, most of which rose up only a few months before the onset of eruption. The observed time changes of velocity anomalies suggest that four-dimensional tomography provides a basis for more efficient volcano monitoring and short- and midterm eruption forecasting of explosive activity.

One hundred volatile years of volcanic gas studies at the Hawaiian Volcano Observatory: Chapter 7 in Characteristics of Hawaiian volcanoes

Science.gov (United States)

Sutton, A.J.; Elias, Tamar; Poland, Michael P.; Takahashi, T. Jane; Landowski, Claire M.

2014-01-01

The first volcanic gas studies in Hawai‘i, beginning in 1912, established that volatile emissions from Kīlauea Volcano contained mostly water vapor, in addition to carbon dioxide and sulfur dioxide. This straightforward discovery overturned a popular volatile theory of the day and, in the same action, helped affirm Thomas A. Jaggar, Jr.’s, vision of the Hawaiian Volcano Observatory (HVO) as a preeminent place to study volcanic processes. Decades later, the environmental movement produced a watershed of quantitative analytical tools that, after being tested at Kīlauea, became part of the regular monitoring effort at HVO. The resulting volatile emission and fumarole chemistry datasets are some of the most extensive on the planet. These data indicate that magma from the mantle enters the shallow magmatic system of Kīlauea sufficiently oversaturated in CO2 to produce turbulent flow. Passive degassing at Kīlauea’s summit that occurred from 1983 through 2007 yielded CO2-depleted, but SO2- and H2O-rich, rift eruptive gases. Beginning with the 2008 summit eruption, magma reaching the East Rift Zone eruption site became depleted of much of its volatile content at the summit eruptive vent before transport to Pu‘u ‘Ō‘ō. The volatile emissions of Hawaiian volcanoes are halogen-poor, relative to those of other basaltic systems. Information gained regarding intrinsic gas solubilities at Kīlauea and Mauna Loa, as well as the pressure-controlled nature of gas release, have provided useful tools for tracking eruptive activity. Regular CO2-emission-rate measurements at Kīlauea’s summit, together with surface-deformation and other data, detected an increase in deep magma supply more than a year before a corresponding surge in effusive activity. Correspondingly, HVO routinely uses SO2 emissions to study shallow eruptive processes and effusion rates. HVO gas studies and Kīlauea’s long-running East Rift Zone eruption also demonstrate that volatile emissions can

Mesoporous Silicate Materials in Sensing

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Paul T. Charles

2008-08-01

Full Text Available Mesoporous silicas, especially those exhibiting ordered pore systems and uniform pore diameters, have shown great potential for sensing applications in recent years. Morphological control grants them versatility in the method of deployment whether as bulk powders, monoliths, thin films, or embedded in coatings. High surface areas and pore sizes greater than 2 nm make them effective as adsorbent coatings for humidity sensors. The pore networks also provide the potential for immobilization of enzymes within the materials. Functionalization of materials by silane grafting or through cocondensation of silicate precursors can be used to provide mesoporous materials with a variety of fluorescent probes as well as surface properties that aid in selective detection of specific analytes. This review will illustrate how mesoporous silicas have been applied to sensing changes in relative humidity, changes in pH, metal cations, toxic industrial compounds, volatile organic compounds, small molecules and ions, nitroenergetic compounds, and biologically relevant molecules.

Constraining the volatile budget of the lunar interior

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Potts, N. J.; Bromiley, G. D.

2017-12-01

Measurements of volatiles (F, Cl, S, H2O) in a range of lunar samples confirm the presence of volatile material in lunar magmas. It remains unknown, however, where this volatile material is stored and when it was delivered to the Moon. On Earth, point defects within mantle olivine, and its high-pressure polymorphs, are thought to be the largest reservoir of volatile material. However, as volatiles have been cycled into and out of the Earth's mantle throughout geological time, via subduction and volcanism, this masks any original volatile signatures. As the Moon has no plate tectonics, it is expected that any volatile material present in the deep lunar interior would have been inherited during accretion and differentiation, providing insight into the delivery of volatiles to the early Earth-Moon system. Our aim was, therefore, to test the volatile storage capacity of the deep lunar mantle and determine mineral/melt partitioning for key volatiles. Experiments were performed in a primitive lunar mantle composition and run at relevant T, P, and at fO2 below the IW buffer. Experiments replicated the initial stages of LMO solidification with either olivine + melt, olivine + pyroxene + melt, or pyroxene + melt as the only phases present. Mineral-melt partition coefficients (Dx) derived for volatile material (F, Cl, S, H2O) vary significantly compared to those derived for terrestrial conditions. An order of magnitude more H2O was found to partition into lunar olivine compared to the terrestrial upper mantle. DF derived for lunar olivine are comparable to the highest terrestrial derived values whilst no Cl was found to partition into lunar olivine under these conditions. Furthermore, an inverse trend between DF and DOH hints towards coupled-substitution mechanisms between H and F under low-fO2/lunar bulk composition. These results suggest that if volatile material was present in the LMO a significant proportion could be partitioned into the lower lunar mantle. The

Subsurface Connections and Magma Mixing as revealed by Olivine- and Pyroxene-Hosted Melt Inclusions from Cerro Negro Volcano and the Las Pilas-El Hoyo Complex, Nicaragua.

Science.gov (United States)

Venugopal, S.; Moune, S.; Williams-Jones, G.

2015-12-01

Cerro Negro, the youngest volcano in the Central American Volcanic Belt, is a polygenetic cinder cone with relatively frequent explosive basaltic eruptions. Las Pilas, on the other hand, is a much larger and older complex with milder and less frequent eruptions. Based on historical data, these two closely spaced volcanoes have shown concurrent eruptive behavior, suggesting a subsurface connection. To further investigate this link, melt inclusions, which are blebs of melt trapped in growing crystals, were the obvious choice for optimal comparison of sources and determination of pre-eruptive volatile contents and magmatic conditions. Olivine-hosted inclusions were chosen for both volcanoes and pyroxene-hosted inclusions were also sampled from Las Pilas to represent the evolved melt. Major, volatile and trace elements reveal a distinct geochemical continuum with Cerro Negro defining the primitive end member and Las Pilas representing the evolved end member. Volatile contents are high for Cerro Negro (up to 1260 ppm CO2, 4.27 wt% H2O and 1700 ppm S) suggesting that volatile exsolution is likely the trigger for Cerro Negro's explosive eruptions. Las Pilas volatile contents are lower but consistent with degassing and evolutionary trends shown by major oxides. Trace element contents are rather unique and suggest Cerro Negro magmas fractionally crystallize while Las Pilas magmas are the products of mixing. Magmatic conditions were estimated with major and volatile contents: at least 2.4 kbar and 1170 °C for Cerro Negro melts and 1.3 kbar and 1130 °C for Las Pilas melts with an overall oxygen fugacity at the NNO buffer. In combination with available literature data, this study suggests an interconnected subsurface plumbing system and thus Cerro Negro should be considered as the newest vent within the Las Pilas-El Hoyo Complex.

Response to Comment on "Rapid cooling and cold storage in a silicic magma reservoir recorded in individual crystals".

Science.gov (United States)

Cooper, Kari M; Till, Christy B; Kent, Adam J R; Costa, Fidel; Rubin, Allison E; Gravley, Darren; Deering, Chad; Cole, Jim; Bose, Maitrayee

2017-12-22

In a recent paper, we used Li concentration profiles and U-Th ages to constrain the thermal conditions of magma storage. Wilson and co-authors argue that the data instead reflect control of Li behavior by charge balance during partitioning and not by experimentally determined diffusion rates. Their arguments are based on (i) a coupled diffusion mechanism for Li, which has been postulated but has not been documented to occur, and (ii) poorly constrained zircon growth rates combined with the assumption of continuous zircon crystallization. Copyright © 2017, American Association for the Advancement of Science.

Artificial magma and applications of the blasting technique

Energy Technology Data Exchange (ETDEWEB)

Ichioka, K [Chugoku Kaki KK, Japan

1974-01-01

Artifical magma is discussed. Solid magma is a high temperature source and fluid magma is also a heat carrier. Iron ores are examples of solid magma, silica-borate is an example of a hydrophobic heat carrier magma assuming a liquid phase at 600/sup 0/C, and S, Ag, Pb, etc. are also examples of heat carrier magma. In addition to these examples, basic salts such as NaNO/sub 3/, KNO/sub 3/, NaCl, CaCl, KCl, BaCl, and Na/sub 4/B/sub 4/O/sub 7/ can be used as artifical magma. These are artifical magmas or heat mediums capable of capturing geothermal heat when circulated inside volcanoes. The blasting technique's applications in geothermal wells are also discussed. The technique can be used to expand a well's diameter, repair the well bottom, regenerate old wells, clean wells, or cut steel pipe. Two figures and one table are provided.

Method for preparation of melts of alkali metal chlorides with highly volatile polyvalent metal chlorides

International Nuclear Information System (INIS)

Salyulev, A.B.; Kudyakov, V.Ya.

1990-01-01

A method for production of alkali metal (Cs, Rb, K) chloride melts with highly volatile polyvalent metal chlorides is suggested. The method consists, in saturation of alkali metal chlorides, preheated to the melting point, by volatile component vapours (titanium tetrachloride, molybdenum or tantalum pentachloride) in proportion, corresponding to the composition reguired. The saturation is realized in an evacuated vessel with two heating areas for 1-1.5 h. After gradual levelling of temperature in both areas the product is rapidly cooled. 1 fig.; 1 tab

Partial reactive crystallization of variable CO2-bearing siliceous MORB-eclogite-derived melt in fertile peridotite and genesis of alkalic basalts with signatures of crustal recycling

Science.gov (United States)

Mallik, A.; Dasgupta, R.

2013-12-01

The presence of heterogeneity in the form of recycled altered oceanic crust (MORB-eclogite) has been proposed in the source of HIMU ocean island basalts (OIBs) [1]. Partial melts of recycled oceanic crust, however, are siliceous and Mg-poor and thus do not resemble the major element compositions of alkalic OIBs that are silica-poor and Mg-rich. In an upwelling heterogenous mantle, MORB-eclogite undergoes melting deeper than volatile-free peridotite, hence, andesitic partial melt derived from eclogite will react with subsolidus peridotite. We have examined the effect of such a melt-rock reaction under volatile-free conditions at 1375 °C, 3 GPa by varying the melt-rock ratio from 8 to 50 wt.% [2]. We concluded that the reacted melts reproduce certain major element characteristics of oceanic basanites, but not nephelinites. Also, the melt-rock reaction produces olivine and garnet-bearing websteritic residue. Because presence of CO2 has been invoked in the source of many HIMU ocean islands, the effect of CO2 on such a melt-rock reaction needs to be evaluated. Accordingly, we performed reaction experiments on mixtures of 25% and 33% CO2-bearing andesitic partial melt and peridotite at 1375 °C, 3 GPa by varying the dissolved CO2 content of the reacting melts from 1 to 5 wt.% (bulk CO2 from 0.25 to 1.6 wt.%) [3, this study]. Owing to melt-rock reaction, with increasing CO2 in the bulk mixture, (a) modes of olivine and cpx decrease while melt, opx and garnet increase, (b) reacted melts evolve to greater degree of Si-undersaturation (from andesite through basanite to nephelinite), (c) enhanced crystallization of garnet take place with higher CO2 in the melt, reducing alumina content of the reacted melts, and (d) CaO and MgO content of the reacted melts increase, without affecting FeO* and Na2O contents (indicating greater propensity of Ca2+ and Mg2+ over Fe2+ and Na+ to enter silicate melt as carbonate). For a given melt-MgO, the CO2-bearing reacted melts are a better

Estimates of volume and magma input in crustal magmatic systems from zircon geochronology: the effect of modelling assumptions and system variables

Directory of Open Access Journals (Sweden)

Luca eCaricchi

2016-04-01

Full Text Available Magma fluxes in the Earth’s crust play an important role in regulating the relationship between the frequency and magnitude of volcanic eruptions, the chemical evolution of magmatic systems and the distribution of geothermal energy and mineral resources on our planet. Therefore, quantifying magma productivity and the rate of magma transfer within the crust can provide valuable insights to characterise the long-term behaviour of volcanic systems and to unveil the link between the physical and chemical evolution of magmatic systems and their potential to generate resources. We performed thermal modelling to compute the temperature evolution of crustal magmatic intrusions with different final volumes assembled over a variety of timescales (i.e., at different magma fluxes. Using these results, we calculated synthetic populations of zircon ages assuming the number of zircons crystallising in a given time period is directly proportional to the volume of magma at temperature within the zircon crystallisation range. The statistical analysis of the calculated populations of zircon ages shows that the mode, median and standard deviation of the populations varies coherently as function of the rate of magma injection and final volume of the crustal intrusions. Therefore, the statistical properties of the population of zircon ages can add useful constraints to quantify the rate of magma injection and the final volume of magmatic intrusions.Here, we explore the effect of different ranges of zircon saturation temperature, intrusion geometry, and wall rock temperature on the calculated distributions of zircon ages. Additionally, we determine the effect of undersampling on the variability of mode, median and standards deviation of calculated populations of zircon ages to estimate the minimum number of zircon analyses necessary to obtain meaningful estimates of magma flux and final intrusion volume.

Examining shear processes during magma ascent

Science.gov (United States)

Kendrick, J. E.; Wallace, P. A.; Coats, R.; Lamur, A.; Lavallée, Y.

2017-12-01

Lava dome eruptions are prone to rapid shifts from effusive to explosive behaviour which reflects the rheology of magma. Magma rheology is governed by composition, porosity and crystal content, which during ascent evolves to yield a rock-like, viscous suspension in the upper conduit. Geophysical monitoring, laboratory experiments and detailed field studies offer the opportunity to explore the complexities associated with the ascent and eruption of such magmas, which rest at a pivotal position with regard to the glass transition, allowing them to either flow or fracture. Crystal interaction during flow results in strain-partitioning and shear-thinning behaviour of the suspension. In a conduit, such characteristics favour the formation of localised shear zones as strain is concentrated along conduit margins, where magma can rupture and heal in repetitive cycles. Sheared magmas often record a history of deformation in the form of: grain size reduction; anisotropic permeable fluid pathways; mineral reactions; injection features; recrystallisation; and magnetic anomalies, providing a signature of the repetitive earthquakes often observed during lava dome eruptions. The repetitive fracture of magma at ( fixed) depth in the conduit and the fault-like products exhumed at spine surfaces indicate that the last hundreds of meters of ascent may be controlled by frictional slip. Experiments on a low-to-high velocity rotary shear apparatus indicate that shear stress on a slip plane is highly velocity dependent, and here we examine how this influences magma ascent and its characteristic geophysical signals.

Pressure Dependence of Komatiite Liquid Viscosity and Implications for Magma Ocean Rheology

Science.gov (United States)

O'Dwyer Brown, L.; Lesher, C. E.; Terasaki, H. G.; Yamada, A.; Sakamaki, T.; Shibazaki, Y.; Ohtani, E.

2009-12-01

The viscosities of komatiite liquids at high pressures and temperatures were investigated using the in-situ falling sphere technique at BL04B1, SPring-8. Komatiites are naturally occurring magmas, rich in network modifying cations. Despite the refractory and fluid nature of komatiite, we successfully measured the viscosity of molten komatiites from Gorgona Island, Colombia (MgO = 17.8 wt.%; NBO/T = 1.5) between 11 and 13 GPa at 2000 C, and from Belingwe, Zimbabwe (MgO = 28.14 wt.%; NBO/T = 2.1) from 12 to 14 GPa at 2000 C. Under isothermal conditions, the viscosity of Gorgona Island komatiite melt increased with pressure, consistent with our previous measurements at lower pressures for this composition. We interpreted this positive pressure dependence as the result of reductions in interatomic space diminishing the free volume of the liquid when compressed. The viscosity of molten komatiite from Belingwe also increased up to 12 GPa, however between 12 and 14 GPa the viscosity is nearly constant. In previous studies of depolymerized silicate liquids, the pressure dependence of viscosity has been shown to reverse from positive to negative between 8 and 10 GPa with corresponding changes in activation volume [1] [2]. In contrast, the activation volume for Belingwe liquid decreases to near zero, but does not become negative above 11 GPa. Similarly, the activation volume for Gorgona Island komatiite remains positive throughout the pressure range investigated. Molecular dynamics simulations of simple MgO-SiO2 liquids with NBO/T > 2 also show a positive pressure dependence, reflecting the dominant control of free-volume reduction on the viscosity of depolymerized melts. However, the more rapid reduction in activation volume with pressure in komatiite liquids may be related to the presence of Al, Ti and other cations that interact and undergo coordination changes unavailable in simple silicate liquids. Along Hadean and post-Hadean mantle adiabats the net effect of

Volatility of components of saturated vapours of UCl/sub 4/-CsCl and UCl/sub 4/-LiCl molten mixtures

Energy Technology Data Exchange (ETDEWEB)

Smirnov, M V; Kudyakov, V Ya; Salyulev, A B; Komarov, V E; Posokhin, Yu V; Afonichkin, V K

1979-01-01

The flow method has been used for measuring the volatility of the components from UCl/sub 4/-CsCl and UCl/sub 4/-LiCl melted mixtures containing 2.0, 5.0, 12.0, 25.0, 33.0, 50.0, 67.0, and 83.0 mol.% of UCl/sub 4/ within the temperature ranges of 903-1188 K and 740-1200 K, respectively. The chemical composition of saturated vapours above the melted salts has been determined. The melted mixtures in question exhibit negative deviation from ideal behaviour. Made was the conclusion about the presence in a vapour phase, along with monomeric UCl/sub 4/, LiCl, CsCl and Li/sub 2/Cl/sub 2/, Cs/sub 2/Cl/sub 2/ dimers of double compounds of the MeUCl/sub 5/ most probable composition. Their absolute contribution into a total pressure above the UCl/sub 4/-CsCl melted mixtures is considerably smaller than above the UCl/sub 4/ -LiCl mixtures.

New high pressure experiments on sulfide saturation of high-FeO∗ basalts with variable TiO2 contents - Implications for the sulfur inventory of the lunar interior

Science.gov (United States)

Ding, Shuo; Hough, Taylor; Dasgupta, Rajdeep

2018-02-01

In order to constrain sulfur concentration in intermediate to high-Ti mare basalts at sulfide saturation (SCSS), we experimentally equilibrated FeS melt and basaltic melt using a piston cylinder at 1.0-2.5 GPa and 1400-1600 °C, with two silicate compositions similar to high-Ti (Apollo 11: A11, ∼11.1 wt.% TiO2, 19.1 wt.% FeO∗, and 39.6 wt.% SiO2) and intermediate-Ti (Luna 16, ∼5 wt.% TiO2, 18.7 wt.% FeO∗, and 43.8 wt.% SiO2) mare basalts. Our experimental results show that SCSS increases with increasing temperature, and decreases with increasing pressure, which are similar to the results from previous experimental studies. SCSS in the A11 melt is systematically higher than that in the Luna 16 melt, which is likely due to higher FeO∗, and lower SiO2 and Al2O3 concentration in the former. Compared to the previously constructed SCSS models, including those designed for high-FeO∗ basalts, the SCSS values determined in this study are generally lower than the predicted values, with overprediction increasing with increasing melt TiO2 content. We attribute this to the lower SiO2 and Al2O3 concentration of the lunar magmas, which is beyond the calibration range of previous SCSS models, and also more abundant FeTiO3 complexes in our experimental melts that have higher TiO2 contents than previous models' calibration range. The formation of FeTiO3 complexes lowers the activity of FeO∗, aFeO∗silicate melt , and therefore causes SCSS to decrease. To accommodate the unique lunar compositions, we have fitted a new SCSS model for basaltic melts of >5 wt.% FeO∗ and variable TiO2 contents. Using previous chalcophile element partitioning experiments that contained more complex Fe-Ni-S sulfide melts, we also derived an empirical correction that allows SCSS calculation for basalts where the equilibrium sulfides contain variable Ni contents of 10-50 wt.%. At the pressures and temperatures of multiple saturation points, SCSS of lunar magmas with compositions from

The Boycott effect in magma chambers

Science.gov (United States)

Blanchette, F.; Peacock, T.; Bush, J. W. M.

2004-03-01

We investigate the plausibility of the stratified Boycott effect as a source of layering in magma chambers. Crystal settling within the magma chamber will generate buoyant fluid near the sloping sidewalls whose vertical ascent may be limited by the ambient stratification associated with vertical gradients in SiO2. The resulting flow may be marked by a layered structure, each layer taking the form of a convection cell spanning the lateral extent of the magma chamber. Using parameters relevant to magma chambers, we estimate that such convection cells would be established over a timescale of a month and have a depth on the order of 4m, which is roughly consistent with field observations of strata within solidified chambers.

Final report on the safety assessment of potassium silicate, sodium metasilicate, and sodium silicate.

Science.gov (United States)

Elmore, Amy R

2005-01-01

Potassium Silicate, Sodium Metasilicate, and Sodium Silicate combine metal cations with silica to form inorganic salts used as corrosion inhibitors in cosmetics. Sodium Metasilicate also functions as a chelating agent and Sodium Silicate as a buffering and pH adjuster. Sodium Metasilicate is currently used in 168 formulations at concentrations ranging from 13% to 18%. Sodium Silicate is currently used in 24 formulations at concentrations ranging from 0.3% to 55%. Potassium Silicate and Sodium Silicate have been reported as being used in industrial cleaners and detergents. Sodium Metasilicate is a GRAS (generally regarded as safe) food ingredient. Aqueous solutions of Sodium Silicate species are a part of a chemical continuum of silicates based on an equilibrium of alkali, water, and silica. pH determines the solubility of silica and, together with concentration, determines the degree of polymerization. Sodium Silicate administered orally is readily absorbed from the alimentary canal and excreted in the urine. The toxicity of these silicates has been related to the molar ratio of SiO2/Na2O and the concentration being used. The Sodium Metasilicate acute oral LD50 ranged from 847 mg/kg in male rats to 1349.3 mg/kg in female rats and from 770 mg/kg in female mice to 820 mg/kg in male mice. Gross lesions of variable severity were found in the oral cavity, pharynx, esophagus, stomach, larynx, lungs, and kidneys of dogs receiving 0.25 g/kg or more of a commercial detergent containing Sodium Metasilicate; similar lesions were also seen in pigs administered the same detergent and dose. Male rats orally administered 464 mg/kg of a 20% solution containing either 2.0 or 2.4 to 1.0 ratio of sodium oxide showed no signs of toxicity, whereas doses of 1000 and 2150 mg/kg produced gasping, dypsnea, and acute depression. Dogs fed 2.4 g/kg/day of Sodium Silicate for 4 weeks had gross renal lesions but no impairment of renal function. Dermal irritation of Potassium Silicate, Sodium

Apatite-Melt Partitioning at 1 Bar: An Assessment of Apatite-Melt Exchange Equilibria Resulting from Non-Ideal Mixing of F and Cl in Apatite

Science.gov (United States)

McCubbin, F. M.; Ustunisik, G.; Vander Kaaden, K. E.

2016-01-01

The mineral apatite [Ca5(PO4)3(F,Cl,OH)] is present in a wide range of planetary materials. Due to the presence of volatiles within its crystal structure (X-site), many recent studies have attempted to use apatite to constrain the volatile contents of planetary magmas and mantle sources. In order to use the volatile contents of apatite to precisely determine the abundances of volatiles in coexisting silicate melt or fluids, thermodynamic models for the apatite solid solution and for the apatite components in multi-component silicate melts and fluids are required. Although some thermodynamic models for apatite have been developed, they are incomplete. Furthermore, no mixing model is available for all of the apatite components in silicate melts or fluids, especially for F and Cl components. Several experimental studies have investigated the apatite-melt and apatite-fluid partitioning behavior of F, Cl, and OH in terrestrial and planetary systems, which have determined that apatite-melt partitioning of volatiles are best described as exchange equilibria similar to Fe-Mg partitioning between olivine and silicate melt. However, McCubbin et al. recently reported that the exchange coefficients may vary in portions of apatite compositional space where F, Cl, and OH do not mix ideally in apatite. In particular, solution calorimetry data of apatite compositions along the F-Cl join exhibit substantial excess enthalpies of mixing. In the present study, we conducted apatite-melt partitioning experiments in evacuated, sealed silica-glass tubes at approximately 1 bar and 950-1050 degrees Centigrade on a synthetic Martian basalt composition equivalent to the basaltic shergottite Queen Alexandria Range (QUE) 94201. These experiments were conducted dry, at low pressure, to assess the effects of temperature and apatite composition on the partitioning behavior of F and Cl between apatite and basaltic melt along the F-Cl apatite binary join, where there is non-ideal mixing of F and Cl

Volatile elements - water, carbon, nitrogen, noble gases - on Earth

Science.gov (United States)

Marty, B.

2017-12-01

Understanding the origin and evolution of life-bearing volatile elements (water, carbon, nitrogen) on Earth is a fruitful and debated area of research. In his pioneering work, W.W. Rubey inferred that the terrestrial atmosphere and the oceans formed from degassing of the mantle through geological periods of time. Early works on noble gas isotopes were consistent with this view and proposed a catastrophic event of mantle degassing early in Earth's history. We now have evidence, mainly from noble gas isotopes, that several cosmochemical sources contributed water and other volatiles at different stages of Earth's accretion. Potential contributors include the protosolar nebula gas that equilibrated with magma oceans, inner solar system bodies now represented by chondrites, and comets. Stable isotope ratios suggest volatiles where primarily sourced by planetary bodies from the inner solar system. However, recent measurements by the European Space Agency Rosetta probe on the coma of Comet 67P/Churyumov-Gerasimenko permit to set quantitative constraints on the cometary contribution to the surface of our planet. The surface and mantle reservoirs volatile elements exchanged volatile elements through time, with rates that are still uncertain. Some mantle regions remained isolated from whole mantle convection within the first tens to hundreds million years after start of solar system formation. These regions, now sampled by some mantle plumes (e.g., Iceland, Eifel) preserved their volatile load, as indicated by extinct and extant radioactivity systems. The abundance of volatile elements in the mantle is still not well known. Different approaches, such as high pressure experimental petrology, noble gas geochemistry, modelling, resulted in somewhat contrasted estimates, varying over one order of magnitude for water. Comparative planetology, that is, the study of volatiles on the Moon, Venus, Mars, Vesta, will shed light on the sources and strengths of these elements in the

Nanostructured silicate polymer concrete

Directory of Open Access Journals (Sweden)

Figovskiy Oleg L'vovich

2014-03-01

Full Text Available It has been known that acid-resistant concretes on the liquid glass basis have high porosity (up to 18~20 %, low strength and insufficient water resistance. Significant increasing of silicate matrix strength and density was carried out by incorporation of special liquid organic alkali-soluble silicate additives, which block superficial pores and reduce concrete shrinkage deformation. It was demonstrated that introduction of tetrafurfuryloxisilane additive sharply increases strength, durability and shock resistance of silicate polymer concrete in aggressive media. The experiments showed, that the strength and density of silicate polymer concrete increase in case of decreasing liquid glass content. The authors obtained optimal content of silicate polymer concrete, which possesses increased strength, durability, density and crack-resistance. Diffusive permeability of concrete and its chemical resistance has been investigated in various corroding media.

Crystallization of a compositionally stratified basal magma ocean

Science.gov (United States)

Laneuville, Matthieu; Hernlund, John; Labrosse, Stéphane; Guttenberg, Nicholas

2018-03-01

Earth's ∼3.45 billion year old magnetic field is regenerated by dynamo action in its convecting liquid metal outer core. However, convection induces an isentropic thermal gradient which, coupled with a high core thermal conductivity, results in rapid conducted heat loss. In the absence of implausibly high radioactivity or alternate sources of motion to drive the geodynamo, the Earth's early core had to be significantly hotter than the melting point of the lower mantle. While the existence of a dense convecting basal magma ocean (BMO) has been proposed to account for high early core temperatures, the requisite physical and chemical properties for a BMO remain controversial. Here we relax the assumption of a well-mixed convecting BMO and instead consider a BMO that is initially gravitationally stratified owing to processes such as mixing between metals and silicates at high temperatures in the core-mantle boundary region during Earth's accretion. Using coupled models of crystallization and heat transfer through a stratified BMO, we show that very high temperatures could have been trapped inside the early core, sequestering enough heat energy to run an ancient geodynamo on cooling power alone.

Magma storage constrains by compositional zoning of plagioclase from dacites of the caldera forming eruptions of Vetrovoy Isthmus and Lvinaya Past’ Bay (Iturup Island, Kurile Islands)

Science.gov (United States)

Maksimovich, I. A.; Smirnov, S. Z.; Kotov, A. A.; Timina, T. Yu; Shevko, A. V.

2017-12-01

The Vetrovoy Isthmus and the Lvinaya Past’ Bay on the Iturup island (Kuril island arc) are the results of large Plinian eruptions of compositionally similar dacitic magmas. This study is devoted to a comparative analysis of the storage and crystallization conditions for magma reservoirs, which were a source of large-scale explosive eruptions. The plagioclase is most informative mineral in studying of the melt evolution. The studied plagioclases possess a complex zoning patterns, which are not typical for silicic rocks in island-arc systems. It was shown that increase of Ca in the plagioclase up to unusually high An95 is related to increase of H2O pressure in both volcanic magma chambers. The study revealed that minerals of the Vetrovoy Isthmus and Lvinaya Past’ crystallized from compositionally similar melts. Despite the compositional similarity of the melts, the phenocryst assemblage of the Lvinaya Past’ differs from the Vetrovoy Isthmus by the presence of the amphibole, which indicates that the pressure in the magmatic chamber exceeded 1-2 kbar at a 4-6 wt. % of H2O in the melt. The rocks of the Vetrovoy Isthmus do not contain amphibole phenocrysts, but melt and fluid inclusions assemblages in plagioclase demonstrate that the magma degassed in the course of evolution. This is an indication that the pressure did not exceed significantly 1-2 kbar.

21 CFR 573.260 - Calcium silicate.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Calcium silicate. 573.260 Section 573.260 Food and... Listing § 573.260 Calcium silicate. Calcium silicate, including synthetic calcium silicate, may be safely used as an anticaking agent in animal feed, provided that the amount of calcium silicate does not...

High-Mg basalts as a Signal of Magma System Replenishment at Lopevi Island, Vanuatu

Science.gov (United States)

Stewart, R. B.; Smith, I. E.; Turner, M. B.; Cronin, S. J.

2007-05-01

Lopevi is is a basalt to basaltic andesite island stratovolcano in central Vanuatu and is part of a long-lived, mature Island Arc chain. Central Vanuatu is tectonically influenced by the subduction of the D'Entrecasteaux zone. Primitive rock types that have been identified from the arc include picrites, ankaramites and high MgO basalts. High MgO rocks are generally considered to be a relatively rare component of arc-type magma suites but as detailed sequence sampling of individual volcanoes occurs, they have been identified more often. Here we report on the occurrence of high-Mg basalts in a sequence of lavas erupted in the last 100 years from Lopevi volcano. Activity at Lopevi is characteristically intermittent with eruptive sequences occurring over a c. 6 year period, separated by longer periods of repose. A major eruptive episode in 1939 caused evacuation of the island and the next eruptive episode in the 1960's also led to evacuation. The 1960's cycle of activity ended in 1982. The most recent phase of activity commenced in 1998 with a return to eruption of more siliceous, high alumina basaltic andesite. Geochemical data show that the 1960's lavas were different from those erupted earlier and later. They are olivine basalts with up to 9 wt percent MgO, 70 ppm Ni and 300 ppm Cr; Al2O3 content is about 12 wt percent. The 2003 lavas and pre-1960's lavas, in contrast, are basaltic andesites with c. 4 wt percent MgO, less than 25 ppm Ni, less than 100 ppm Cr and c. 20 wt percent Al2O3. The 1960's Lopevi sequence of eruptions represents an injection of a more primitive, high MgO magma at the end of a 21 year quiescent period after the major eruptions of 1939. Injection of small batches of more primitive magmas over decadal time periods at Lopevi marks the initiation of a new magmatic cycle. The occurrence of high MgO magmas as part of a cycle that includes typically low MgO arc type rocks demonstrates a consanguineous relationship and shows that high MgO arc type

The Magma Chamber Simulator: Modeling the Impact of Wall Rock Composition on Mafic Magmas during Assimilation-Fractional Crystallization

Science.gov (United States)

Creamer, J. B.; Spera, F. J.; Bohrson, W. A.; Ghiorso, M. S.

2012-12-01

Although stoichiometric titration is often used to model the process of concurrent Assimilation and Fractional Crystallization (AFC) within a compositionally evolving magma body, a more complete treatment of the problem involves simultaneous and self-consistent determination of stable phase relationships and separately evolving temperatures of both Magma (M) and Wall Rock (WR) that interact as a composite M-WR system. Here we present results of M-WR systems undergoing AFC forward modeled with the Magma Chamber Simulator (MCS), which uses the phase modeling capabilities of MELTS (Ghiorso & Sack 1995) as the thermodynamic basis. Simulations begin with one of a variety of mafic magmas (e.g. HAB, MORB, AOB) intruding a set mass of Wall Rock (e.g. lherzolite, gabbro, diorite, granite, metapelite), and heat is exchanged as the M-WR system proceeds towards thermal equilibrium. Depending on initial conditions, the early part of the evolution can involve closed system FC while the WR heats up. The WR behaves as a closed system until it is heated beyond the solidus to critical limit for melt fraction extraction (fc), ranging between 0.08 and 0.12 depending on WR characteristics including composition and, rheology and stress field. Once fc is exceeded, a portion of the anatectic liquid is assimilated into the Magma. The MCS simultaneously calculates mass and composition of the mineral assemblage (Magma cumulates and WR residue) and melt (anatectic and Magma) at each T along the equilibration trajectory. Sensible and latent heat lost or gained plus mass gained by the Magma are accounted for by the MCS via governing Energy Constrained- Recharge Assimilation Fractional Crystallization (EC-RAFC) equations. In a comparison of two representative MCS results, consider a granitic WR intruded by HAB melt (51 wt. % SiO2) at liquidus T in shallow crust (0.1 GPa) with a WR/M ratio of 1.25, fc of 0.1 and a QFM oxygen buffer. In the first example, the WR begins at a temperature of 100o

Numerical modeling of bubble dynamics in magmas

Science.gov (United States)

Huber, Christian; Su, Yanqing; Parmigiani, Andrea

2014-05-01

Understanding the complex non-linear physics that governs volcanic eruptions is contingent on our ability to characterize the dynamics of bubbles and its effect on the ascending magma. The exsolution and migration of bubbles has also a great impact on the heat and mass transport in and out of magma bodies stored at shallow depths in the crust. Multiphase systems like magmas are by definition heterogeneous at small scales. Although mixture theory or homogenization methods are convenient to represent multiphase systems as a homogeneous equivalent media, these approaches do not inform us on possible feedbacks at the pore-scale and can be significantly misleading. In this presentation, we discuss the development and application of bubble-scale multiphase flow modeling to address the following questions : How do bubbles impact heat and mass transport in magma chambers ? How efficient are chemical exchanges between the melt and bubbles during magma decompression? What is the role of hydrodynamic interactions on the deformation of bubbles while the magma is sheared? Addressing these questions requires powerful numerical methods that accurately model the balance between viscous, capillary and pressure stresses. We discuss how these bubble-scale models can provide important constraints on the dynamics of magmas stored at shallow depth or ascending to the surface during an eruption.

[Study on two preparation methods for beta-CD inclusion compound of four traditional Chinese medicine volatile oils].

Science.gov (United States)

Li, Hailiang; Cui, Xiaoli; Tong, Yan; Gong, Muxin

2012-04-01

To compare inclusion effects and process conditions of two preparation methods-colloid mill and saturated solution-for beta-CD inclusion compound of four traditional Chinese medicine volatile oils and study the relationship between each process condition and volatile oil physical properties and the regularity of selective inclusion of volatile oil components. Volatile oils from Nardostachyos Radix et Rhizoma, Amomi Fructus, Zingiberis Rhizoma and Angelicaesinensis Radix were prepared using two methods in the orthogonal test. These inclusion compounds by optimized processes were assessed and compared by such methods as TLC, IR and scanning electron microscope. Inclusion oils were extracted by steam distillation, and the components found before and after inclusion were analyzed by GC-MS. Analysis showed that new inclusion compounds, but inclusion compounds prepared by the two processes had differences to some extent. The colloid mill method showed a better inclusion effect than the saturated solution method, indicating that their process conditions had relations with volatile oil physical properties. There were differences in the inclusion selectivity of components between each other. The colloid mill method for inclusion preparation is more suitable for industrial requirements. To prepare volatile oil inclusion compounds with heavy gravity and high refractive index, the colloid mill method needs longer time and more water, while the saturated solution method requires higher temperature and more beta-cyclodextrin. The inclusion complex prepared with the colloid mill method contains extended molecular weight chemical composition, but the kinds of components are reduced.

Comparative Magma Oceanography

Science.gov (United States)

Jones, J. H.

1999-01-01

The question of whether the Earth ever passed through a magma ocean stage is of considerable interest. Geochemical evidence strongly suggests that the Moon had a magma ocean and the evidence is mounting that the same was true for Mars. Analyses of martian (SNC) meteorites have yielded insights into the differentiation history of Mars, and consequently, it is interesting to compare that planet to the Earth. Three primary features of Mars contrast strongly to those of the Earth: (i) the extremely ancient ages of the martian core, mantle, and crust (about 4.55 b.y.); (ii) the highly depleted nature of the martian mantle; and (iii) the extreme ranges of Nd isotopic compositions that arise within the crust and depleted mantle. The easiest way to explain the ages and diverse isotopic compositions of martian basalts is to postulate that Mars had an early magma ocean. Cumulates of this magma ocean were later remelted to form the SNC meteorite suite and some of these melts assimilated crustal materials enriched in incompatible elements. The REE pattern of the crust assimilated by these SNC magmas was LREE enriched. If this pattern is typical of the crust as a whole, the martian crust is probably similar in composition to melts generated by small degrees of partial melting (about 5%) of a primitive source. Higher degrees of partial melting would cause the crustal LREE pattern to be essentially flat. In the context of a magma ocean model, where large degrees of partial melting presumably prevailed, the crust would have to be dominated by late-stage, LREE-enriched residual liquids. Regardless of the exact physical setting, Nd and W isotopic evidence indicates that martian geochemical reservoirs must have formed early and that they have not been efficiently remixed since. The important point is that in both the Moon and Mars we see evidence of a magma ocean phase and that we recognize it as such. Several lines of theoretical inference point to an early Earth that was also hot

Magma Dynamics at Yucca Mountain, Nevada

Energy Technology Data Exchange (ETDEWEB)

D. Krier

2005-08-29

Small-volume basaltic volcanic activity at Yucca Mountain has been identified as one of the potential events that could lead to release of radioactive material from the U.S. Department of Energy (DOE) designated nuclear waste repository at Yucca Mountain. Release of material could occur indirectly as a result of magmatic dike intrusion into the repository (with no associated surface eruption) by changing groundwater flow paths, or as a result of an eruption (dike intrusion of the repository drifts, followed by surface eruption of contaminated ash) or volcanic ejection of material onto the Earth's surface and the redistribution of contaminated volcanic tephra. Either release method includes interaction between emplacement drifts and a magmatic dike or conduit, and natural (geologic) processes that might interrupt or halt igneous activity. This analysis provides summary information on two approaches to evaluate effects of disruption at the repository by basaltic igneous activity: (1) descriptions of the physical geometry of ascending basaltic dikes and their interaction with silicic host rocks similar in composition to the repository host rocks; and (2) a summary of calculations developed to quantify the response of emplacement drifts that have been flooded with magma and repressurized following blockage of an eruptive conduit. The purpose of these analyses is to explore the potential consequences that could occur during the full duration of an igneous event.

Magma Dynamics at Yucca Mountain, Nevada

International Nuclear Information System (INIS)

D. Krier

2005-01-01

Small-volume basaltic volcanic activity at Yucca Mountain has been identified as one of the potential events that could lead to release of radioactive material from the U.S. Department of Energy (DOE) designated nuclear waste repository at Yucca Mountain. Release of material could occur indirectly as a result of magmatic dike intrusion into the repository (with no associated surface eruption) by changing groundwater flow paths, or as a result of an eruption (dike intrusion of the repository drifts, followed by surface eruption of contaminated ash) or volcanic ejection of material onto the Earth's surface and the redistribution of contaminated volcanic tephra. Either release method includes interaction between emplacement drifts and a magmatic dike or conduit, and natural (geologic) processes that might interrupt or halt igneous activity. This analysis provides summary information on two approaches to evaluate effects of disruption at the repository by basaltic igneous activity: (1) descriptions of the physical geometry of ascending basaltic dikes and their interaction with silicic host rocks similar in composition to the repository host rocks; and (2) a summary of calculations developed to quantify the response of emplacement drifts that have been flooded with magma and repressurized following blockage of an eruptive conduit. The purpose of these analyses is to explore the potential consequences that could occur during the full duration of an igneous event

Grain to outcrop-scale frozen moments of dynamic magma mixing in the syenite magma chamber, Yelagiri Alkaline Complex, South India

Directory of Open Access Journals (Sweden)

M.L. Renjith

2014-11-01

Full Text Available Magma mixing process is unusual in the petrogenesis of felsic rocks associated with alkaline complex worldwide. Here we present a rare example of magma mixing in syenite from the Yelagiri Alkaline Complex, South India. Yelagiri syenite is a reversely zoned massif with shoshonitic (Na2O + K2O=5–10 wt.%, Na2O/K2O = 0.5–2, TiO2 <0.7 wt.% and metaluminous character. Systematic modal variation of plagioclase (An11–16 Ab82–88, K-feldspar (Or27–95 Ab5–61, diopside (En34–40Fs11–18Wo46–49, biotite, and Ca-amphibole (edenite build up three syenite facies within it and imply the role of in-situ fractional crystallization (FC. Evidences such as (1 disequilibrium micro-textures in feldspars, (2 microgranular mafic enclaves (MME and (3 synplutonic dykes signify mixing of shoshonitic mafic magma (MgO = 4–5 wt.%, SiO2 = 54–59 wt.%, K2O/Na2O = 0.4–0.9 with syenite. Molecular-scale mixing of mafic magma resulted disequilibrium growth of feldspars in syenite. Physical entity of mafic magma preserved as MME due to high thermal-rheological contrast with syenite magma show various hybridization through chemical exchange, mechanical dilution enhanced by chaotic advection and phenocryst migration. In synplutonic dykes, disaggregation and mixing of mafic magma was confined within the conduit of injection. Major-oxides mass balance test quantified that approximately 0.6 portions of mafic magma had interacted with most evolved syenite magma and generated most hybridized MME and dyke samples. It is unique that all the rock types (syenite, MME and synplutonic dykes share similar shoshonitic and metaluminous character; mineral chemistry, REE content, coherent geochemical variation in Harker diagram suggest that mixing of magma between similar composition. Outcrop-scale features of crystal accumulation and flow fabrics also significant along with MME and synplutonic dykes in syenite suggesting that Yelagiri syenite magma chamber had evolved

Halogen degassing during ascent and eruption of water-poor basaltic magma

Science.gov (United States)

Edmonds, M.; Gerlach, T.M.; Herd, Richard A.

2009-01-01

A study of volcanic gas composition and matrix glass volatile concentrations has allowed a model for halogen degassing to be formulated for K??lauea Volcano, Hawai'i. Volcanic gases emitted during 2004-2005 were characterised by a molar SO2/HCl of 10-64, with a mean of 33; and a molar HF/HCl of 0-5, with a mean of 1.0 (from approximately 2500 measurements). The HF/HCl ratio was more variable than the SO2/HCl ratio, and the two correlate weakly. Variations in ratio took place over rapid timescales (seconds). Matrix glasses of Pele's tears erupted in 2006 have a mean S, Cl and F content of 67, 85 and 173??ppm respectively, but are associated with a large range in S/F. A model is developed that describes the open system degassing of halogens from parental magmas, using the glass data from this study, previously published results and parameterisation of sulphur degassing from previous work. The results illustrate that halogen degassing takes place at pressures of < 1??MPa, equivalent to < ~ 35??m in the conduit. Fluid-melt partition coefficients for Cl and F are low (< 1.5); F only degasses appreciably at < 0.1??MPa above atmospheric pressure, virtually at the top of the magma column. This model reproduces the volcanic gas data and other observations of volcanic activity well and is consistent with other studies of halogen degassing from basaltic magmas. The model suggests that variation in volcanic gas halogen ratios is caused by exsolution and gas-melt separation at low pressures in the conduit. There is no evidence that either diffusive fractionation or near-vent chemical reactions involving halogens is important in the system, although these processes cannot be ruled out. The fluxes of HCl and HF from K??lauea during 2004-5 were ~ 25 and 12??t/d respectively. ?? 2008 Elsevier B.V.

Pre-eruptive conditions of dacitic magma erupted during the 21.7 ka Plinian event at Nevado de Toluca volcano, Central Mexico

Science.gov (United States)

Arce, J. L.; Gardner, J. E.; Macías, J. L.

2013-01-01

The Nevado de Toluca volcano in Central Mexico has been active over the last ca. 42 ka, during which tens of km3 of pyroclastic material were erupted and two important Plinian-type eruptions occurred at ca. 21.7 ka (Lower Toluca Pumice: LTP) and ca. 10.5 ka (Upper Toluca Pumice: UTP). Samples from both the LTP and UTP contain plagioclase, amphibole, iron-titanium oxides, and minor anhedral biotite, set in a vesicular, rhyolitic, glassy matrix. In addition, UTP dacites contain orthopyroxene. Analysis of melt inclusions in plagioclase phenocrysts yields H2O contents of 2-3.5 wt.% for LTP and 1.3-3.6 wt.% for UTP samples. Ilmenite-ulvospinel geothermometry yields an average temperature of ~ 868 °C for the LTP magma (hotter than the UTP magma, ~ 842 °C; Arce et al., 2006), whereas amphibole-plagioclase geothermometry yields a temperature of 825-859 °C for the LTP magma. Water-saturated experiments using LTP dacite suggest that: (i) amphibole is stable above 100 MPa and below 900 °C; (ii) plagioclase crystallizes below 250-100 MPa at temperatures of 850-900 °C; and (iii) pyroxene is stable only below pressures of 200-100 MPa and temperatures of 825-900 °C. Comparison of natural and experimental data suggests that the LTP dacitic magma was stored at 150-200 MPa (5.8-7.7 km below the volcano summit). No differences in pressure found between 21.7 ka and 10.5 ka suggest that these two magmas were stored at similar depths. Orthopyroxene produced in lower temperature LTP experiments is compositionally different to those found in UTP natural samples, suggesting that they originated in two different magma batches. Whole-rock chemistry, petrographic features, and mineral compositions suggest that magma mixing was responsible for the generation of the dacitic Plinian LTP eruption.

Degassing vs. eruptive styles at Mt. Etna volcano (Sicily, Italy): Volatile stocking, gas fluxing, and the shift from low-energy to highly-explosive basaltic eruptions

Science.gov (United States)

Moretti, Roberto; Métrich, Nicole; Di Renzo, Valeria; Aiuppa, Alessandro; Allard, Patrick; Arienzo, Ilenia

2017-04-01

Basaltic magmas can transport and release large amounts of volatiles into the atmosphere, especially in subduction zones, where slab-derived fluids enrich the mantle wedge. Depending on magma volatile content, basaltic volcanoes thus display a wide spectrum of eruptive styles, from common Strombolian-type activity to Plinian events. Mt. Etna in Sicily, is a typical basaltic volcano where the volatile control on such a variable activity can be investigated. Based on a melt inclusion study in products from Strombolian or lava-fountain activity to Plinian eruptions, here we show that for the same initial volatile content, different eruptive styles reflect variable degassing paths throughout the composite Etnean plumbing system. The combined influence of i) crystallization, ii) deep degassing and iii) CO2 gas fluxing can explain the evolution of H2O, CO2, S and Cl in products from such a spectrum of activity. Deep crystallization produces the CO2-rich gas fluxing the upward magma portions, which will become buoyant and easily mobilized in small gas-rich batches stored within the plumbing system. When reaching gas dominated conditions (i.e., a gas/melt mass ratio of 0.3 and CO2,gas/H2Ogas molar ratio 5 ), these will erupt effusively or mildly explosively, whilst in case of the 122 BC Plinian eruption, open-system degassing conditions took place within the plumbing system, such that continuous CO2-fluxing determined gas accumulation on top of the magmatic system. The emission of such a cap in the early eruptive phase triggered the arrival of deep H2O-rich whose fast decompression and bubble nucleation lead to the highly explosive character, enhanced by abundant microlite crystallization and consequent increase of magma effective viscosity. This could explain why open system basaltic systems like Etna may experience highly explosive or even Plinian episodes during eruptions that start with effusive to mildly explosive phases. The proposed mechanism also determines a

Xe isotopic constraints on cycling of deep Earth volatiles

Science.gov (United States)

Parai, R.; Mukhopadhyay, S.

2017-12-01

The modern deep Earth volatile budget reflects primordial volatiles delivered during accretion, radiogenic ingrowth of volatile species (e.g., 40Ar produced by 40K decay), outgassing in association with mantle processing, and regassing via subduction. The noble gases are unique volatile tracers in that they are chemically inert, but are thought to be trapped within hydrous alteration phases in downwelling lithologies. Noble gases thus provide a tracer of volatile transport between the deep Earth and surface reservoirs. Constraints on the fluxes of noble gases between deep Earth and surface reservoirs over time can accordingly be used to provide insight into temperature conditions at subduction zones, limits on volatile cycling, and the evolving distribution of major volatile species in terrestrial reservoirs over time. Xe isotope systematics in mantle-derived rocks show that 80-90% of the mantle Xe budget is derived from recycling of atmospheric Xe, indicating that atmospheric Xe is retained in subducting slabs beyond depths of magma generation in subduction zones over Earth history. We present an integrated model of Xe cycling between the mantle and atmosphere in association with mantle processing over Earth history. We test a wide variety of outgassing and regassing rates and take the evolution of the atmospheric Xe isotopic composition [e.g., 1] into account. Models in which the deep Earth transitions from a net outgassing to net regassing regime best satisfy Xe isotopic constraints from mantle-derived rocks [2-6]. [1] Avice et al., 2017; Nature Communications, 8; [2] Mukhopadhyay, 2012, Nature 486, 101-104; [3] Parai et al., 2012, EPSL 359-360, 227-239; [4] Parai and Mukhopadhay, 2015, G-cubed 16, 719-735; [5] Peto et al., 2013, EPSL 369-370, 13-23; [6] Tucker et al., 2012, EPSL 355-356, 244-254.

Modeling Silicate Weathering for Elevated CO2 and Temperature

Science.gov (United States)

Bolton, E. W.

2016-12-01

A reactive transport model (RTM) is used to assess CO2 drawdown by silicate weathering over a wide range of temperature, pCO2, and infiltration rates for basalts and granites. Although RTM's have been used extensively to model weathering of basalts and granites for present-day conditions, we extend such modeling to higher CO2 that could have existed during the Archean and Proterozoic. We also consider a wide range of surface temperatures and infiltration rates. We consider several model basalt and granite compositions. We normally impose CO2 in equilibrium with the various atmospheric ranges modeled and CO2 is delivered to the weathering zone by aqueous transport. We also consider models with fixed CO2 (aq) throughout the weathering zone as could occur in soils with partial water saturation or with plant respiration, which can strongly influence pH and mineral dissolution rates. For the modeling, we use Kinflow: a model developed at Yale that includes mineral dissolution and precipitation under kinetic control, aqueous speciation, surface erosion, dynamic porosity, permeability, and mineral surface areas via sub-grid-scale grain models, and exchange of volatiles at the surface. Most of the modeling is done in 1D, but some comparisons to 2D domains with heterogeneous permeability are made. We find that when CO2 is fixed only at the surface, the pH tends toward higher values for basalts than granites, in large part due to the presence of more divalent than monovalent cations in the primary minerals, tending to decrease rates of mineral dissolution. Weathering rates increase (as expected) with increasing CO2 and temperature. This modeling is done with the support of the Virtual Planetary Laboratory.

Interaction of coeval felsic and mafic magmas from the Kanker ...

Indian Academy of Sciences (India)

66

20 crystallization of the latter, results in hybrid magmas under the influence of thermal and. 21 chemical exchange. The mechanical exchange occurs between the coexisting magmas due to. 22 viscosity contrast, if the mafic magma enters slightly later into the magma chamber, when the. 23 felsic magma started to crystallize.

Infrared spectroscopy of dust in the Taurus dark clouds: ice and silicates

International Nuclear Information System (INIS)

Whittet, D.C.B.; Adamson, A.J.; McFadzean, A.D.; Aitken, D.K.

1988-01-01

Low-resolution spectra are presented of the 3 μm water-ice and 10 μm silicate dust features for stars in the direction of the extensive dark cloud complex in Taurus. A total of 22 stars were observed at 3 μm, and 16 at 10 μm. Our sample includes both dust-embedded objects and background field stars seen through the cloud. New and previously published results are combined to investigate the correlation of the strengths of both features with visual extinction A v , and we demonstrate the existence of a very close linear correlation between the peak optical depth in the 3 μm feature and A v for field stars. Ice is detected in all cases where A v exceeds a threshold value of 3.3 ± 0.1 mag, a result which provides a firm observational basis for models of volatile mantle growth on grains in the dark cloud environment. In contrast, the silicate feature is rather poorly correlated with A v . (author)

Depth of origin of magma in eruptions.

Science.gov (United States)

Becerril, Laura; Galindo, Ines; Gudmundsson, Agust; Morales, Jose Maria

2013-09-26

Many volcanic hazard factors--such as the likelihood and duration of an eruption, the eruption style, and the probability of its triggering large landslides or caldera collapses--relate to the depth of the magma source. Yet, the magma source depths are commonly poorly known, even in frequently erupting volcanoes such as Hekla in Iceland and Etna in Italy. Here we show how the length-thickness ratios of feeder dykes can be used to estimate the depth to the source magma chamber. Using this method, accurately measured volcanic fissures/feeder-dykes in El Hierro (Canary Islands) indicate a source depth of 11-15 km, which coincides with the main cloud of earthquake foci surrounding the magma chamber associated with the 2011-2012 eruption of El Hierro. The method can be used on widely available GPS and InSAR data to calculate the depths to the source magma chambers of active volcanoes worldwide.

Mantle enrichment by volatiles as the Nazca plate subducts beneath the Payenia backarc of the Southern Volcanic Zone, Argentina

DEFF Research Database (Denmark)

Brandt, Frederik Ejvang

The thesis is a contribution towards the understanding of the generation of the source mantle for magmas related to the subduction of the Nazca plate under South America with an emphasis on the geochemistry of the volatiles Cl, F, S, H2O and CO2. The study presents analytical data for tephra, min...

Constraining magma physical properties and its temporal evolution from InSAR and topographic data only: a physics-based eruption model for the effusive phase of the Cordon Caulle 2011-2012 rhyodacitic eruption

Science.gov (United States)

Delgado, F.; Kubanek, J.; Anderson, K. R.; Lundgren, P.; Pritchard, M. E.

2017-12-01

The 2011-2012 eruption of Cordón Caulle volcano in Chile is the best scientifically observed rhyodacitic eruption and is thus a key place to understand the dynamics of these rare but powerful explosive rhyodacitic eruptions. Because the volatile phase controls both the eruption temporal evolution and the eruptive style, either explosive or effusive, it is important to constrain the physical parameters that drive these eruptions. The eruption began explosively and after two weeks evolved into a hybrid explosive - lava flow effusion whose volume-time evolution we constrain with a series of TanDEM-X Digital Elevation Models. Our data shows the intrusion of a large volume laccolith or cryptodome during the first 2.5 months of the eruption and lava flow effusion only afterwards, with a total volume of 1.4 km3. InSAR data from the ENVISAT and TerraSAR-X missions shows more than 2 m of subsidence during the effusive eruption phase produced by deflation of a finite spheroidal source at a depth of 5 km. In order to constrain the magma total H2O content, crystal cargo, and reservoir pressure drop we numerically solve the coupled set of equations of a pressurized magma reservoir, magma conduit flow and time dependent density, volatile exsolution and viscosity that we use to invert the InSAR and topographic data time series. We compare the best-fit model parameters with independent estimates of magma viscosity and total gas content measured from lava samples. Preliminary modeling shows that although it is not possible to model both the InSAR and the topographic data during the onset of the laccolith emplacement, it is possible to constrain the magma H2O and crystal content, to 4% wt and 30% which agree well with published literature values.

Transmission X-ray Diffraction (XRD) Patterns Relevant to the MSL Chemin Amorphous Component: Sulfates And Silicates

Science.gov (United States)

Morris, R. V.; Rampe, E. B.; Graff, T. G.; Archer, P. D., Jr.; Le, L.; Ming, D. W.; Sutter, B.

2015-01-01

The Mars Science Laboratory (MSL) CheMin instrument on the Curiosity rover is a transmission X-ray diffractometer (Co-Kalpha radiation source and a approx.5deg to approx.52deg 2theta range) where the analyzed powder samples are constrained to have discrete particle diameters XRD amorphous component. Estimates of amorphous component abundance, based on the XRD data itself and on mass-balance calculations using APXS data crystalline component chemistry derived from XRD data, martian meteorites, and/or stoichiometry [e.g., 6-9], range from approx.20 wt.% to approx.50 wt.% of bulk sample. The APXSbased calculations show that the amorphous component is rich in volatile elements (esp. SO3) and is not simply primary basaltic glass, which was used as a surrogate to model the broad band in the RN CheMin pattern. For RN, the entire volatile inventory (except minor anhydrite) is assigned to the amorphous component because no volatile-bearing crystalline phases were reported within detection limits [2]. For JK and CB, Fesaponite, basanite, and akaganeite are volatile-bearing crystalline components. Here we report transmission XRD patterns for sulfate and silicate phases relevant to interpretation of MSL-CheMin XRD amorphous components.

Zircons reveal magma fluxes in the Earth's crust.

Science.gov (United States)

Caricchi, Luca; Simpson, Guy; Schaltegger, Urs

2014-07-24

Magma fluxes regulate the planetary thermal budget, the growth of continents and the frequency and magnitude of volcanic eruptions, and play a part in the genesis and size of magmatic ore deposits. However, because a large fraction of the magma produced on the Earth does not erupt at the surface, determinations of magma fluxes are rare and this compromises our ability to establish a link between global heat transfer and large-scale geological processes. Here we show that age distributions of zircons, a mineral often present in crustal magmatic rocks, in combination with thermal modelling, provide an accurate means of retrieving magma fluxes. The characteristics of zircon age populations vary significantly and systematically as a function of the flux and total volume of magma accumulated in the Earth's crust. Our approach produces results that are consistent with independent determinations of magma fluxes and volumes of magmatic systems. Analysis of existing age population data sets using our method suggests that porphyry-type deposits, plutons and large eruptions each require magma input over different timescales at different characteristic average fluxes. We anticipate that more extensive and complete magma flux data sets will serve to clarify the control that the global heat flux exerts on the frequency of geological events such as volcanic eruptions, and to determine the main factors controlling the distribution of resources on our planet.

Using fumarolic inert gas composition to investigate magma dynamics at Campi Flegrei (Italy)

Science.gov (United States)

Chiodini, G.; Caliro, S.; Paonita, A.; Cardellini, C.

2013-12-01

volatiles, inert gases are the preferred species to achieve information on the dynamics and structure of the magma plumbing systems.

Variations in magma supply rate at Kilauea Volcano, Hawaii

Science.gov (United States)

Dvorak, John J.; Dzurisin, Daniel

1993-01-01

When an eruption of Kilauea lasts more than 4 months, so that a well-defined conduit has time to develop, magma moves freely through the volcano from a deep source to the eruptive site at a constant rate of 0.09 km3/yr. At other times, the magma supply rate to Kilauea, estimated from geodetic measurements of surface displacements, may be different. For example, after a large withdrawal of magma from the summit reservoir, such as during a rift zone eruption, the magma supply rate is high initially but then lessens and exponentially decays as the reservoir refills. Different episodes of refilling may have different average rates of magma supply. During four year-long episodes in the 1960s, the annual rate of refilling varied from 0.02 to 0.18 km3/yr, bracketing the sustained eruptive rate of 0.09 km3/yr. For decade-long or longer periods, our estimate of magma supply rate is based on long-term changes in eruptive rate. We use eruptive rate because after a few dozen eruptions the volume of magma that passes through the summit reservoir is much larger than the net change of volume of magma stored within Kilauea. The low eruptive rate of 0.009 km3/yr between 1840 and 1950, compared to an average eruptive rate of 0.05 km3/yr since 1950, suggests that the magma supply rate was lower between 1840 and 1950 than it has been since 1950. An obvious difference in activity before and since 1950 was the frequency of rift zone eruptions: eight rift zone eruptions occurred between 1840 and 1950, but more than 20 rift zone eruptions have occurred since 1950. The frequency of rift zone eruptions influences magma supply rate by suddenly lowering pressure of the summit magma reservoir, which feeds magma to rift zone eruptions. A temporary drop of reservoir pressure means a larger-than-normal pressure difference between the reservoir and a deeper source, so magma is forced to move upward into Kilauea at a faster rate.

21 CFR 172.410 - Calcium silicate.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Calcium silicate. 172.410 Section 172.410 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN... Agents § 172.410 Calcium silicate. Calcium silicate, including synthetic calcium silicate, may be safely...

Insights into the emplacement of upper-crustal plutons and their relationship to large silicic calderas, from field relationships, geochronology, and zircon trace element geochemistry in the Stillwater - Clan Alpine caldera complex, western Nevada, USA

Science.gov (United States)

Colgan, Joseph P.; John, David A.; Henry, Christopher D.; Watts, Kathryn E.

2018-01-01

Geologic mapping, new U-Pb zircon ages, and new and published 40Ar/39Ar sanidine ages document the timing and extent of Oligocene magmatism in the southern Stillwater Range and Clan Alpine Mountains of western Nevada, where Miocene extension has exposed at least six nested silicic calderas and underlying granitic plutons to crustal depths locally ≥ 9 km. Both caldera-forming rhyolitic tuffs and underlying plutons were emplaced in two episodes, one from about 30.4-28.2 Ma that included the Deep Canyon, Job Canyon, and Campbell Creek calderas and underlying plutons, and one from about 25.3-24.8 Ma that included the Louderback Mountains, Poco Canyon, and Elevenmile Canyon calderas and underlying plutons. In these two 1-2 m.y. periods, almost the entire Mesozoic upper crust was replaced by Oligocene intrusive and extrusive rocks to depths ≥ 9 km over an estimated total area of 1500 km2 (pre-extension). Zircon trace element geochemistry indicates that some plutonic rock can be solidified residual magma from the tuff eruptions. Most plutons are not solidified residual magma, although they directly underlie calderas and were emplaced along the same structures shortly after to as much as one million years after caldera formation. Magma chambers and plutons grew by floor subsidence accommodated by downward transfer of country rocks. If other Great Basin calderas are similar, the dense concentration of shallowly exposed calderas in central Nevada is underlain by a complexly zoned mid-Cenozoic batholith assembled in discrete pulses that coincided with formation of large silicic calderas up to 2500-5000 km3.

Experimental determination of the Mo isotope fractionation factor between metal and silicate liquids

Science.gov (United States)

Hin, R. C.; Burkhardt, C.; Schmidt, M. W.; Bourdon, B.

2011-12-01

The conditions and chemical consequences of core formation have mainly been reconstructed from experimentally determined element partition coefficients between metal and silicate liquids. However, first order questions such as the mode of core formation or the nature of the light element(s) in the Earth's core are still debated [1]. In addition, the geocentric design of most experimental studies leaves the conditions of core formation on other terrestrial planets and asteroids even more uncertain than for Earth. Through mass spectrometry, records of mass-dependent stable isotope fractionation during high-temperature processes such as metal-silicate segregation are detectable. Stable isotope fractionation may thus yield additional constrains on core formation conditions and its consequences for the chemical evolution of planetary objects. Experimental investigations of equilibrium mass-dependent stable isotope fractionation have shown that Si isotopes fractionate between metal and silicate liquids at temperatures of 1800°C and pressures of 1 GPa, while Fe isotopes leave no resolvable traces of core formation processes [2,3]. Molybdenum is a refractory and siderophile trace element in the Earth, and thus much less prone to complications arising from mass balancing core and mantle and from potential volatile behaviour than other elements. To determine equilibrium mass-dependent Mo isotope fractionation during metal-silicate segregation, we have designed piston cylinder experiments with a basaltic silicate composition and an iron based metal with ~8 wt% Mo, using both graphite and MgO capsules. Metal and silicate phases are completely segregated by the use of a centrifuging piston cylinder at ETH Zurich, thus preventing analysis of mixed metal and silicate signatures. Molybdenum isotope compositions were measured using a Nu Instruments 1700 MC-ICP-MS at ETH Zurich. To ensure an accurate correction of analytical mass fractionation a 100Mo-97Mo double spike was admixed

Distribution of Alkalis (Na, Cs, Rb) Between Silicate and Sulfide: Implications for Planetary Volatile Depletion

Science.gov (United States)

Boujibar, A.; Fei, Y.; Righter, K.; Du, Z.; Bullock, E.

2018-01-01

The abundances of volatile elements in the Earth's mantle are correlated with their temperatures of condensation. This depletion can be due to either incomplete condensation of the elements during the nebula condensation or evaporation processes during planetary growth. Elements that have affinities with metals (siderophile) and sulfides (chalcophile) are additionally depleted due to their segregation into the core. Therefore, study of lithophile elements could be useful to isolate processes of volatilization and their effect on the abundance of the elements in the Earth's mantle. However, the correlation of these lithophile elements including alkali elements, with their temperatures of condensation shows a significant scatter, which is difficult to reconcile with a depletion by vaporization or incomplete condensation alone.

MAGMA: analysis of two-channel microarrays made easy.

Science.gov (United States)

Rehrauer, Hubert; Zoller, Stefan; Schlapbach, Ralph

2007-07-01

The web application MAGMA provides a simple and intuitive interface to identify differentially expressed genes from two-channel microarray data. While the underlying algorithms are not superior to those of similar web applications, MAGMA is particularly user friendly and can be used without prior training. The user interface guides the novice user through the most typical microarray analysis workflow consisting of data upload, annotation, normalization and statistical analysis. It automatically generates R-scripts that document MAGMA's entire data processing steps, thereby allowing the user to regenerate all results in his local R installation. The implementation of MAGMA follows the model-view-controller design pattern that strictly separates the R-based statistical data processing, the web-representation and the application logic. This modular design makes the application flexible and easily extendible by experts in one of the fields: statistical microarray analysis, web design or software development. State-of-the-art Java Server Faces technology was used to generate the web interface and to perform user input processing. MAGMA's object-oriented modular framework makes it easily extendible and applicable to other fields and demonstrates that modern Java technology is also suitable for rather small and concise academic projects. MAGMA is freely available at www.magma-fgcz.uzh.ch.

Forecasting magma-chamber rupture at Santorini volcano, Greece.

Science.gov (United States)

Browning, John; Drymoni, Kyriaki; Gudmundsson, Agust

2015-10-28

How much magma needs to be added to a shallow magma chamber to cause rupture, dyke injection, and a potential eruption? Models that yield reliable answers to this question are needed in order to facilitate eruption forecasting. Development of a long-lived shallow magma chamber requires periodic influx of magmas from a parental body at depth. This redistribution process does not necessarily cause an eruption but produces a net volume change that can be measured geodetically by inversion techniques. Using continuum-mechanics and fracture-mechanics principles, we calculate the amount of magma contained at shallow depth beneath Santorini volcano, Greece. We demonstrate through structural analysis of dykes exposed within the Santorini caldera, previously published data on the volume of recent eruptions, and geodetic measurements of the 2011-2012 unrest period, that the measured 0.02% increase in volume of Santorini's shallow magma chamber was associated with magmatic excess pressure increase of around 1.1 MPa. This excess pressure was high enough to bring the chamber roof close to rupture and dyke injection. For volcanoes with known typical extrusion and intrusion (dyke) volumes, the new methodology presented here makes it possible to forecast the conditions for magma-chamber failure and dyke injection at any geodetically well-monitored volcano.

Mush Column Magma Chambers

Science.gov (United States)

Marsh, B. D.

2002-12-01

Magma chambers are a necessary concept in understanding the chemical and physical evolution of magma. The concept may well be similar to a transfer function in circuit or time series analysis. It does what needs to be done to transform source magma into eruptible magma. In gravity and geodetic interpretations the causative body is (usually of necessity) geometrically simple and of limited vertical extent; it is clearly difficult to `see' through the uppermost manifestation of the concentrated magma. The presence of plutons in the upper crust has reinforced the view that magma chambers are large pots of magma, but as in the physical representation of a transfer function, actual magma chambers are clearly distinct from virtual magma chambers. Two key features to understanding magmatic systems are that they are vertically integrated over large distances (e.g., 30-100 km), and that all local magmatic processes are controlled by solidification fronts. Heat transfer considerations show that any viable volcanic system must be supported by a vertically extensive plumbing system. Field and geophysical studies point to a common theme of an interconnected stack of sill-like structures extending to great depth. This is a magmatic Mush Column. The large-scale (10s of km) structure resembles the vertical structure inferred at large volcanic centers like Hawaii (e.g., Ryan et al.), and the fine scale (10s to 100s of m) structure is exemplified by ophiolites and deeply eroded sill complexes like the Ferrar dolerites of the McMurdo Dry Valleys, Antarctica. The local length scales of the sill reservoirs and interconnecting conduits produce a rich spectrum of crystallization environments with distinct solidification time scales. Extensive horizontal and vertical mushy walls provide conditions conducive to specific processes of differentiation from solidification front instability to sidewall porous flow and wall rock slumping. The size, strength, and time series of eruptive behavior

Environmental silicate nano-biocomposites

CERN Document Server

Pollet, Eric

2012-01-01

Environmental Silicate Nano-Biocomposites focuses on nano-biocomposites, which are obtained by the association of silicates such as bioclays with biopolymers. By highlighting recent developments and findings, green and biodegradable nano-composites from both renewable and biodegradable polymers are explored. This includes coverage of potential markets such as packaging, agricultures, leisure and the fast food industry. The knowledge and experience of more than twenty international experts in diverse fields, from chemical and biochemical engineering to applications, is brought together in four different sections covering: Biodegradable polymers and Silicates, Clay/Polyesters Nano-biocomposites, Clay/Agropolymers Nano-biocomposites, and Applications and biodegradation of Nano-biocomposites. By exploring the relationships between the biopolymer structures, the processes, and the final properties Environmental Silicate Nano-Biocomposites explains how to design nano-materials to develop new, valuable, environmenta...

SILICATE COMPOSITION OF THE INTERSTELLAR MEDIUM

International Nuclear Information System (INIS)

Fogerty, S.; Forrest, W.; Watson, D. M.; Koch, I.; Sargent, B. A.

2016-01-01

The composition of silicate dust in the diffuse interstellar medium and in protoplanetary disks around young stars informs our understanding of the processing and evolution of the dust grains leading up to planet formation. An analysis of the well-known 9.7 μ m feature indicates that small amorphous silicate grains represent a significant fraction of interstellar dust and are also major components of protoplanetary disks. However, this feature is typically modeled assuming amorphous silicate dust of olivine and pyroxene stoichiometries. Here, we analyze interstellar dust with models of silicate dust that include non-stoichiometric amorphous silicate grains. Modeling the optical depth along lines of sight toward the extinguished objects Cyg OB2 No. 12 and ζ Ophiuchi, we find evidence for interstellar amorphous silicate dust with stoichiometry intermediate between olivine and pyroxene, which we simply refer to as “polivene.” Finally, we compare these results to models of silicate emission from the Trapezium and protoplanetary disks in Taurus.

SILICATE COMPOSITION OF THE INTERSTELLAR MEDIUM

Energy Technology Data Exchange (ETDEWEB)

Fogerty, S.; Forrest, W.; Watson, D. M.; Koch, I. [Department of Physics and Astronomy, University of Rochester, Rochester, NY 14627 (United States); Sargent, B. A., E-mail: sfogerty@pas.rochester.edu [Center for Imaging Science and Laboratory for Multiwavelength Astrophysics, Rochester Institute of Technology, 54 Lomb Memorial Drive, Rochester, NY 14623 (United States)

2016-10-20

The composition of silicate dust in the diffuse interstellar medium and in protoplanetary disks around young stars informs our understanding of the processing and evolution of the dust grains leading up to planet formation. An analysis of the well-known 9.7 μ m feature indicates that small amorphous silicate grains represent a significant fraction of interstellar dust and are also major components of protoplanetary disks. However, this feature is typically modeled assuming amorphous silicate dust of olivine and pyroxene stoichiometries. Here, we analyze interstellar dust with models of silicate dust that include non-stoichiometric amorphous silicate grains. Modeling the optical depth along lines of sight toward the extinguished objects Cyg OB2 No. 12 and ζ Ophiuchi, we find evidence for interstellar amorphous silicate dust with stoichiometry intermediate between olivine and pyroxene, which we simply refer to as “polivene.” Finally, we compare these results to models of silicate emission from the Trapezium and protoplanetary disks in Taurus.

Silica-enriched mantle sources of subalkaline picrite-boninite-andesite island arc magmas

Science.gov (United States)

Bénard, A.; Arculus, R. J.; Nebel, O.; Ionov, D. A.; McAlpine, S. R. B.

2017-02-01

Primary arc melts may form through fluxed or adiabatic decompression melting in the mantle wedge, or via a combination of both processes. Major limitations to our understanding of the formation of primary arc melts stem from the fact that most arc lavas are aggregated blends of individual magma batches, further modified by differentiation processes in the sub-arc mantle lithosphere and overlying crust. Primary melt generation is thus masked by these types of second-stage processes. Magma-hosted peridotites sampled as xenoliths in subduction zone magmas are possible remnants of sub-arc mantle and magma generation processes, but are rarely sampled in active arcs. Published studies have emphasised the predominantly harzburgitic lithologies with particularly high modal orthopyroxene in these xenoliths; the former characteristic reflects the refractory nature of these materials consequent to extensive melt depletion of a lherzolitic protolith whereas the latter feature requires additional explanation. Here we present major and minor element data for pristine, mantle-derived, lava-hosted spinel-bearing harzburgite and dunite xenoliths and associated primitive melts from the active Kamchatka and Bismarck arcs. We show that these peridotite suites, and other mantle xenoliths sampled in circum-Pacific arcs, are a distinctive peridotite type not found in other tectonic settings, and are melting residues from hydrous melting of silica-enriched mantle sources. We explore the ability of experimental studies allied with mantle melting parameterisations (pMELTS, Petrolog3) to reproduce the compositions of these arc peridotites, and present a protolith ('hybrid mantle wedge') composition that satisfies the available constraints. The composition of peridotite xenoliths recovered from erupted arc magmas plausibly requires their formation initially via interaction of slab-derived components with refractory mantle prior to or during the formation of primary arc melts. The liquid

Unraveling the diversity in arc volcanic eruption styles: Examples from the Aleutian volcanic arc, Alaska

Science.gov (United States)

Larsen, Jessica F.

2016-11-01

The magmatic systems feeding arc volcanoes are complex, leading to a rich diversity in eruptive products and eruption styles. This review focuses on examples from the Aleutian subduction zone, encompassed within the state of Alaska, USA because it exhibits a rich diversity in arc structure and tectonics, sediment and volatile influx feeding primary magma generation, crustal magma differentiation processes, with the resulting outcome the production of a complete range in eruption styles from its diverse volcanic centers. Recent and ongoing investigations along the arc reveal controls on magma production that result in diversity of eruptive products, from crystal-rich intermediate andesites to phenocryst-poor, melt-rich silicic and mafic magmas and a spectrum in between. Thus, deep to shallow crustal "processing" of arc magmas likely greatly influences the physical and chemical character of the magmas as they accumulate in the shallow crust, the flow physics of the magmas as they rise in the conduit, and eruption style through differences in degassing kinetics of the bubbly magmas. The broad spectrum of resulting eruption styles thus depends on the bulk magma composition, melt phase composition, and the bubble and crystal content (phenocrysts and/or microlites) of the magma. Those fundamental magma characteristics are in turn largely determined by the crustal differentiation pathway traversed by the magma as a function of tectonic location in the arc, and/or the water content and composition of the primary magmas. The physical and chemical character of the magma, set by the arc differentiation pathway, as it ascends towards eruption determines the kinetic efficiency of degassing versus the increasing internal gas bubble overpressure. The balance between degassing rate and the rate at which gas bubble overpressure builds then determines the conditions of fragmentation, and ultimately eruption intensity.

Coccolithophores and calcite saturation state in the Baltic and Black Seas

Directory of Open Access Journals (Sweden)

T. Tyrrell

2008-04-01

Full Text Available The Baltic and Black Seas are both brackish, that is to say both have salinities intermediate between freshwater and seawater. The coccolithophore Emiliania huxleyi is abundant in one, the Black Sea, but absent from the other, the Baltic Sea. Here we present summertime coccolithophore measurements confirming this difference, as well as data on the calcium carbonate saturation state of the Baltic Sea. We find that the Baltic Sea becomes undersaturated (or nearly so in winter, with respect to both the aragonite and calcite mineral forms of CaCO₃. Data for the Black Sea are more limited, but it appears to remain strongly supersaturated year-round. The absence of E. huxleyi from the Baltic Sea could therefore potentially be explained by dissolution of their coccoliths in winter, suggesting that minimum annual (wintertime saturation states could be most important in determining future ocean acidification impacts. In addition to this potential importance of winter saturation state, alternative explanations are also possible, either related to differences in salinity or else to differences in silicate concentrations.

Pre-eruptive conditions of the Hideaway Park topaz rhyolite: Insights into metal source and evolution of magma parental to the Henderson porphyry molybdenum deposit, Colorado

Science.gov (United States)

Mercer, Celestine N.; Hofstra, Albert H.; Todorov, Todor I.; Roberge, Julie; Burgisser, Alain; Adams, David T.; Cosca, Michael A.

2015-01-01

The Hideaway Park tuff is the only preserved extrusive volcanic unit related to the Red Mountain intrusive complex, which produced the world-class Henderson porphyry Mo deposit. Located within the Colorado Mineral Belt, USA, Henderson is the second largest Climax-type Mo deposit in the world, and is therefore an excellent location to investigate magmatic processes leading to Climax-type Mo mineralization. We combine an extensive dataset of major element, volatile, and trace element abundances in quartz-hosted melt inclusions and pumice matrix glass with major element geochemistry from phenocrysts to reconstruct the pre-eruptive conditions and the source and evolution of metals within the magma. Melt inclusions are slightly peraluminous topaz rhyolitic in composition and are volatile-charged (≤6 wt % H2O, ≤600 ppm CO2, ∼0·3–1·0 wt % F, ∼2300–3500 ppm Cl) and metal-rich (∼7–24 ppm Mo, ∼4–14 ppm W, ∼21–52 ppm Pb, ∼28–2700 ppm Zn, shallow ascent and eruption. Filter pressing, crystal settling, magma recharge and mixing of less evolved rhyolite melt, and volatile exsolution were important processes during magma evolution; the low estimated viscosities (∼105–1010 Pa s) of these H2O- and F-rich melts probably enhanced these processes. A noteworthy discrepancy between the metal contents in the pumice matrix glass and in the melt inclusions suggests that after quartz crystallization ceased upon shallow magma ascent and eruption, the Hideaway Park magma exsolved an aqueous fluid into which Mo, Bi, Ag, Zn, Mn, Cs, and Y strongly partitioned. Given that the Henderson deposit contains anomalous abundances of not only Mo, but also W, Pb, Zn, Cu, Bi, Ag, and Mn, we suggest that these metals were sourced from similar fluids exsolved from unerupted portions of the same magmatic system. Trace element ratios imply that Mo was sourced deep, from either the lower crust or metasomatized mantle. The origin of sulfur remains unresolved

Modifying Silicates for Better Dispersion in Nanocomposites

Science.gov (United States)

Campbell, Sandi

2005-01-01

An improved chemical modification has been developed to enhance the dispersion of layered silicate particles in the formulation of a polymer/silicate nanocomposite material. The modification involves, among other things, the co-exchange of an alkyl ammonium ion and a monoprotonated diamine with interlayer cations of the silicate. The net overall effects of the improved chemical modification are to improve processability of the nanocomposite and maximize the benefits of dispersing the silicate particles into the polymer. Some background discussion is necessary to give meaning to a description of this development. Polymer/silicate nanocomposites are also denoted polymer/clay composites because the silicate particles in them are typically derived from clay particles. Particles of clay comprise layers of silicate platelets separated by gaps called "galleries." The platelet thickness is 1 nm. The length varies from 30 nm to 1 m, depending on the silicate. In order to fully realize the benefits of polymer/silicate nanocomposites, it is necessary to ensure that the platelets become dispersed in the polymer matrices. Proper dispersion can impart physical and chemical properties that make nanocomposites attractive for a variety of applications. In order to achieve nanometer-level dispersion of a layered silicate into a polymer matrix, it is typically necessary to modify the interlayer silicate surfaces by attaching organic functional groups. This modification can be achieved easily by ion exchange between the interlayer metal cations found naturally in the silicate and protonated organic cations - typically protonated amines. Long-chain alkyl ammonium ions are commonly chosen as the ion-exchange materials because they effectively lower the surface energies of the silicates and ease the incorporation of organic monomers or polymers into the silicate galleries. This completes the background discussion. In the present improved modification of the interlayer silicate surfaces

Comparison of two methods for extraction of volatiles from marine PL emulsions

DEFF Research Database (Denmark)

Lu, Henna Fung Sieng; Nielsen, Nina Skall; Jacobsen, Charlotte

2013-01-01

The dynamic headspace (DHS) thermal desorption principle using Tenax GR tube, as well as the solid phase micro‐extraction (SPME) tool with carboxen/polydimethylsiloxane 50/30 µm CAR/PDMS SPME fiber, both coupled to GC/MS were implemented for the isolation and identification of both lipid...... and Strecker derived volatiles in marine phospholipids (PL) emulsions. Comparison of volatile extraction efficiency was made between the methods. For marine PL emulsions with a highly complex composition of volatiles headspace, a fiber saturation problem was encountered when using CAR/PDMS‐SPME for volatiles...... analysis. However, the CAR/PDMS‐SPME technique was efficient for lipid oxidation analysis in emulsions of less complex headspace. The SPME method extracted volatiles of lower molecular weights more efficient than the DHS method. On the other hand, DHS Tenax GR appeared to be more efficient in extracting...

Geochemical modeling of the influence of silicate mineral alteration on alkalinity production and carbonate precipitation

Science.gov (United States)

Herda, Gerhard; Kraemer, Stephan M.; Gier, Susanne; Meister, Patrick

2016-04-01

High CO2 partial pressure (pCO2) in deep rock reservoirs causes acidification of the porefluid. Such conditions occur during injection and subsurface storage of CO2 (to prevent the release of greenhouse gas) but also naturally in zones of strong methanogenic microbial activity in organic matter-rich ocean margin sediments. The acidic fluids are corrosive to carbonates and bear the risk of leakage of CO2 gas to the surface. Porefluid acidification may be moderated by processes that increase the alkalinity, i.e. that produce weak acid anions capable of buffering the acidification imposed by the CO2. Often, alkalinity increases as a result of anaerobic microbial activity, such as anaerobic oxidation of methane. However, on a long term the alteration of silicates, in particular, clay minerals, may be a more efficient mechanism of alkalinity production. Under altered temperature, pressure and porefluid composition at depth, clay minerals may change to thermodynamically more stable states, thereby increasing the alkalinity of the porefluid by partial leaching of Mg-(OH)2 and Ca-(OH)2 (e.g. Wallmann et al., 2008; Mavromatis et al., 2014). This alteration may even be enhanced by a high pCO2. Thus, silicate alteration can be essential for a long-term stabilization of volatile CO2 in the form of bicarbonate or may even induce precipitation of carbonate minerals, but these processes are not fully understood yet. The goal of this study is to simulate the alkalinity effect of silicate alteration under diagenetic conditions and high pCO2 by geochemical modeling. We are using the program PHREEQC (Parkhurst and Appelo, 2013) to generate high rock/fluid ratio characteristics for deep subsurface rock reservoirs. Since we are interested in the long-term evolution of diagenetic processes, over millions of years, we do not consider kinetics but calculate the theoretically possible equilibrium conditions. In a first step we are calculating the saturation state of different clay minerals

Deep pooling of low degree melts and volatile fluxes at the 85°E segment of the Gakkel Ridge: Evidence from olivine-hosted melt inclusions and glasses

Science.gov (United States)

Shaw, Alison M.; Behn, Mark D.; Humphris, Susan E.; Sohn, Robert A.; Gregg, Patricia M.

2010-01-01

We present new analyses of volatile, major, and trace elements for a suite of glasses and melt inclusions from the 85°E segment of the ultra-slow spreading Gakkel Ridge. Samples from this segment include limu o pele and glass shards, proposed to result from CO 2-driven explosive activity. The major element and volatile compositions of the melt inclusions are more variable and consistently more primitive than the glass data. CO 2 contents in the melt inclusions extend to higher values (167-1596 ppm) than in the co-existing glasses (187-227 ppm), indicating that the melt inclusions were trapped at greater depths. These melt inclusions record the highest CO 2 melt concentrations observed for a ridge environment. Based on a vapor saturation model, we estimate that the melt inclusions were trapped between seafloor depths (˜ 4 km) and ˜ 9 km below the seafloor. However, the glasses are all in equilibrium with their eruption depths, which is inconsistent with the rapid magma ascent rates expected for explosive activity. Melting conditions inferred from thermobarometry suggest relatively deep (25-40 km) and cold (1240°-1325 °C) melting conditions, consistent with a thermal structure calculated for the Gakkel Ridge. The water contents and trace element compositions of the melt inclusions and glasses are remarkably homogeneous; this is an unexpected result for ultra-slow spreading ridges, where magma mixing is generally thought to be less efficient based on the assumption that steady-state crustal magma chambers are absent in these environments. All melts can be described by a single liquid line of descent originating from a pooled melt composition that is consistent with the aggregate melt calculated from a geodynamic model for the Gakkel Ridge. These data suggest a model in which deep, low degree melts are efficiently pooled in the upper mantle (9-20 km depth), after which crystallization commences and continues during ascent and eruption. Based on our melting model

Petrological constraints on the recycling of mafic crystal mushes, magma ascent and intrusion of braided sills in the Torres del Paine mafic complex (Patagonia)

Science.gov (United States)

Leuthold, Julien; Müntener, Othmar; Baumgartner, Lukas; Putlitz, Benita

2014-05-01

Cumulate and crystal mush disruption and reactivation are difficult to recognise in coarse grained shallow plutonic rocks. Mafic minerals included in hornblende and zoned plagioclase provide snapshots of early crystallization and cumulate formation, but are difficult to interpret in terms of the dynamics of magma ascent and possible links between silicic and mafic rock emplacement. We will present the field relations, the microtextures and the mineral chemistry of the Miocene mafic sill complex of the Torres del Paine intrusive complex (Patagonia, Chile) and its sub-vertical feeder-zone. The mafic sill complex was built up by a succession of braided sills of shoshonitic and high-K calc-alkaline porphyritic hornblende-gabbro and fine grained monzodioritic sills. The mafic units were over-accreted over 41±11 ka, underplating the overlying granite. Local diapiric structures and felsic magma accumulation between sills indicate limited separation of intercumulus liquid from the mafic sills. Anhedral hornblende cores, with olivine + clinopyroxene ± plagioclase ± apatite inclusions, crystallized at temperatures >900°C and pressures of ~300 to ~500 MPa. The corresponding rims and monzodiorite matrix crystallized at 950°C) from the middle crust reservoir to the emplacement level. We show that hornblende-plagioclase thermobarometry is a useful monitor for the determination of segregation conditions of granitic magmas from gabbroic crystal mushes, and for monitoring the evolution of shallow crustal magmatic crystallization, decompression and cooling.

Determination of the solubility of low volatility liquid organic compounds in water using volatile-tracer assisted headspace gas chromatography.

Science.gov (United States)

Zhang, Shu-Xin; Chai, Xin-Sheng; Barnes, Donald G

2016-02-26

This study reports a new headspace gas chromatographic method (HS-GC) for the determination of water solubility of low volatility liquid organic compounds (LVLOs). The HS-GC analysis was performed on a set of aqueous solutions containing a range of concentrations of toluene-spiked (as a tracer) LVLOs, from under-saturation to over-saturation. A plot of the toluene tracer GC signal vs. the concentration of the LVLO results in two lines of different slopes that intersect at the concentration corresponding to the compound's solubility in water. The results showed that the HS-GC method has good precision (RSD waters of environmental and biological systems. Copyright © 2016 Elsevier B.V. All rights reserved.

Magma-derived CO2 emissions in the Tengchong volcanic field, SE Tibet: Implications for deep carbon cycle at intra-continent subduction zone

Science.gov (United States)

Zhang, Maoliang; Guo, Zhengfu; Sano, Yuji; Zhang, Lihong; Sun, Yutao; Cheng, Zhihui; Yang, Tsanyao Frank

2016-09-01

Active volcanoes at oceanic subduction zone have long been regard as important pathways for deep carbon degassed from Earth's interior, whereas those at continental subduction zone remain poorly constrained. Large-scale active volcanoes, together with significant modern hydrothermal activities, are widely distributed in the Tengchong volcanic field (TVF) on convergent boundary between the Indian and Eurasian plates. They provide an important opportunity for studying deep carbon cycle at the ongoing intra-continent subduction zone. Soil microseepage survey based on accumulation chamber method reveals an average soil CO2 flux of ca. 280 g m-2 d-1 in wet season for the Rehai geothermal park (RGP). Combined with average soil CO2 flux in dry season (ca. 875 g m-2 d-1), total soil CO2 output of the RGP and adjacent region (ca. 3 km2) would be about 6.30 × 105 t a-1. Additionally, we conclude that total flux of outgassing CO2 from the TVF would range in (4.48-7.05) × 106 t a-1, if CO2 fluxes from hot springs and soil in literature are taken into account. Both hot spring and soil gases from the TVF exhibit enrichment in CO2 (>85%) and remarkable contribution from mantle components, as indicated by their elevated 3He/4He ratios (1.85-5.30 RA) and δ13C-CO2 values (-9.00‰ to -2.07‰). He-C isotope coupling model suggests involvement of recycled organic metasediments and limestones from subducted Indian continental lithosphere in formation of the enriched mantle wedge (EMW), which has been recognized as source region of the TVF parental magmas. Contamination by crustal limestone is the first-order control on variations in He-CO2 systematics of volatiles released by the EMW-derived melts. Depleted mantle and recycled crustal materials from subducted Indian continental lithosphere contribute about 45-85% of the total carbon inventory, while the rest carbon (about 15-55%) is accounted by limestones in continental crust. As indicated by origin and evolution of the TVF

Ground surface deformation patterns, magma supply, and magma storage at Okmok volcano, Alaska, from InSAR analysis: 1. Intereruption deformation, 1997–2008

Science.gov (United States)

Lu, Zhong; Dzurisin, Daniel; Biggs, Juliet; Wicks, Charles; McNutt, Steve

2010-01-01

Starting soon after the 1997 eruption at Okmok volcano and continuing until the start of the 2008 eruption, magma accumulated in a storage zone centered ~3.5 km beneath the caldera floor at a rate that varied with time. A Mogi-type point pressure source or finite sphere with a radius of 1 km provides an adequate fit to the deformation field portrayed in time-sequential interferometric synthetic aperture radar images. From the end of the 1997 eruption through summer 2004, magma storage increased by 3.2–4.5 × 107 m3, which corresponds to 75–85% of the magma volume erupted in 1997. Thereafter, the average magma supply rate decreased such that by 10 July 2008, 2 days before the start of the 2008 eruption, magma storage had increased by 3.7–5.2 × 107 m3 or 85–100% of the 1997 eruption volume. We propose that the supply rate decreased in response to the diminishing pressure gradient between the shallow storage zone and a deeper magma source region. Eventually the effects of continuing magma supply and vesiculation of stored magma caused a critical pressure threshold to be exceeded, triggering the 2008 eruption. A similar pattern of initially rapid inflation followed by oscillatory but generally slowing inflation was observed prior to the 1997 eruption. In both cases, withdrawal of magma during the eruptions depressurized the shallow storage zone, causing significant volcano-wide subsidence and initiating a new intereruption deformation cycle.

Major and trace element and volatile constraints on magma systematics of seamounts and axial ridge glasses from the East Pacific Rise between 8°N and 12°N

Science.gov (United States)

Lytle, M. L.; Kelley, K. A.; Wanless, V. D.; Hauri, E. H.

2017-12-01

The East Pacific Rise is a fast spreading mid-ocean ridge system (6-16cm/yr) consisting of many spreading ridges and transform faults. Focusing on a well-studied segment between 8-12°N, we present new SIMS measurements of magmatic volatiles (H2O, CO2, S, Cl, F) and new LA-ICP-MS trace element data in both on-axis and off-axis glasses, coupled with previously published data and use these data to relate melt composition to crystallization and melting processes. The seamounts range in composition from evolved (MgO = 5.54 wt%) to fairly primitive (MgO = 9.70 wt%), whereas on-axis samples have a narrower range of MgO (5.85 - 8.83 wt%). Seamounts span a wide range of enrichment in trace element compositions (La/Sm 0.45 - 4.63; Th/La 0.02 - 0.14; K/Ti 0.02 - 0.66), whereas on-axis glasses reflect NMORB compositions (La/Sm 0.5 - 1; Th/La 0.035 - 0.07; K/Ti 0.05 - 0.15). Light rare earth elements in the seamounts vary from depleted to enriched and have variable Eu anomalies (0.79 - 1.10), while on-axis samples have NMORB patterns with more negative Eu anomalies (0.74 - 1.00). The H2O content of the seamounts ranges from dry (0.05 wt%) to fairly wet (0.96 wt%), whereas on-axis samples have a narrower range (0.15 - 0.31 wt%). Cl contents show variable mixing between seawater and a magmatic component, with seamounts assimilating more seawater. Magmatic liquid lines of descent (LLD), recorded in glass, reflect fractional crystallization of olivine, plagioclase, and clinopyroxene, consistent with modal phenocryst abundances of the rocks. A multi-element approach (e.g., MgO vs. Al2O3, CaO, CaO/Al2O3), constrains LLDs, providing fractionation slopes, allowing mafic basalt compositions to be accurately corrected back to primary melts in equilibrium with Fo90. Using these melts, pressures and temperatures of melt equilibration can be constrained using melt thermobarometry. On-axis samples reflect higher PT conditions (1371°C; 1.37 GPa), although within error of seamounts (1340�

Oxygen isotopes and volatile contents of the Gorgona komatiites, Colombia: A confirmation of the deep mantle origin of H2O

Science.gov (United States)

Gurenko, Andrey A.; Kamenetsky, Vadim S.; Kerr, Andrew C.

2016-11-01

We report O isotopes in olivine grains (Fo89-93) and volatile contents (CO2, H2O, F, S, Cl) in olivine-hosted melt inclusions from one Gorgona picrite and five komatiites with the aim of constraining the origin of H2O in these magmas. These samples have previously been analysed for major and trace elements and volatile concentrations (H2O, S, Cl) and B isotopes in melt inclusions. A distinctive feature of the included melts is relatively high contents of volatile components and boron, which show positive anomalies in, otherwise depleted, primitive mantle normalised trace and rare earth element patterns and range in δ11 B from -11.5 to 15.6‰. In this study, the olivines were systematically analysed for O isotopes (1) in the centre of grains, (2) near the grain boundaries and, (3) as close as possible to the studied melt inclusions. The majority of olivines (∼66%) are ;mantle;-like, 4.8 ‰ ≤δ18 O ≤ 5.5 ‰, with a subordinate but still significant number (∼33%) above, and only 2 grains below, this range. There is no systematic difference between the central and marginal parts of the grains. Higher than ;mantle; δ18OOl values are ascribed to low-T (Gorgona mafic and ultramafic magmas.

Magma chamber interaction giving rise to asymmetric oscillations

Science.gov (United States)

Walwer, D.; Ghil, M.; Calais, E.

2017-12-01

Geodetic time series at four volcanoes (Okmok, Akutan, Shishaldin, and Réunion) are processed using Multi-channel Singular Spectrum Analysis (M-SSA) and reveal sawtooth-shaped oscillations ; the latter are characterized by short intervals of fast inflations followed by longer intervals of slower deflations. At Okmok and Akutan, the oscillations are first damped and then accentuated. At Okmok, the increase in amplitude of the oscillations is followed by an eruption. We first show that the dynamics of these four volcanoes bears similarities with that of a simple nonlinear, dissipative oscillator, indicating that the inflation-deflation episodes are relaxation oscillations. These observations imply that ab initio dynamical models of magma chambers should possess an asymmetric oscillatory regime. Next, based on the work of Whitehead and Helfrich [1991], we show that a model of two magma chambers — connected by a cylindrical conduit in which the magma viscosity depends on temperature — gives rise to asymmetric overpressure oscillations in the magma reservoirs. These oscillations lead to surface deformations that are consistent with those observed at the four volcanoes in this study. This relaxation oscillation regime occurs only when the vertical temperature gradient in the host rock between the two magma chambers is large enough and when the magma flux entering the volcanic system is sufficiently high. The magma being supplied by a deeper source region, the input flux depends on the pressure difference between the source and the deepest reservoir. When this difference is not sufficiently high, the magma flux exponentially decreases, leading to damped oscillations as observed at Akutan and Okmok. The combination of observational and modeling results clearly supports the role of relaxation oscillations in the dynamics of volcanic systems.

Space-weathering processes and products on volatile-rich asteroids

Science.gov (United States)

Britt, D.; Schelling, P.; Consolmagno, G.; Bradley, T.

2014-07-01

Space weathering is a generic term for the effects on atmosphereless solid bodies in the solar system from a range of processes associated with direct exposure to the space environment. These include impact processes (shock, vaporization, fragmentation, heating, melting, and ejecta formation), radiation damage (from galactic and solar cosmic rays), solar-wind effects (irradiation, ion implantation, and sputtering), and the chemical reactions driven by these processes. The classic example of space weathering is the formation of the lunar spectral red slope associated with the production of nanophase Fe (npFe0) in the dusty lunar regolith (C.R. Chapman, 2004, Annual Review of Earth & Planet. Sci. 32, C.M. Pieters, 2000, MAPS 35). Similar npFe0 has been recovered from asteroid (25143) Itokawa and some asteroid classes do exhibit modest spectral red slopes (T. Noguchi, 2011, Science 333). Space weathering can be thought of as driven by a combination of the chemical environment of space (hard vacuum, low oxygen fugacity, solar-wind implantation of hydrogen) along with thermal energy supplied by micrometeorite impacts. The forward modeling of space weathering as thermodynamically-driven decomposition of common rock-forming minerals suggests the production of a range of daughter products: (1) The silicate products typically lose oxygen, other volatile elements (i.e., sulfur and sodium), and metallic cations, producing minerals that are typically more disordered and less optically active than the original parent materials. (2) The decomposed metallic cations form in nano-sized blebs including npFe0, on the surfaces or in condensing rims of mineral grains. This creates a powerful optical component as seen in the lunar red slope. Surfaces with exposed npFe0 are an ideal environment for catalyzing further reactions. (3) The liberated volatile elements and gases (O, S, Na) may form an observable exosphere (e.g., Moon and Mercury) and can either escape from the body or

On magma fragmentation by conduit shear stress: Evidence from the Kos Plateau Tuff, Aegean Volcanic Arc

Science.gov (United States)

Palladino, Danilo M.; Simei, Silvia; Kyriakopoulos, Konstantinos

2008-12-01

Large silicic explosive eruptions are the most catastrophic volcanic events. Yet, the intratelluric mechanisms underlying are not fully understood. Here we report a field and laboratory study of the Kos Plateau Tuff (KPT, 161 ka, Aegean Volcanic Arc), which provides an excellent geological example of conduit processes that control magma vesiculation and fragmentation during intermediate- to large-scale caldera-forming eruptions. A prominent feature of the KPT is the occurrence of quite unusual platy-shaped tube pumice clasts in pyroclastic fall and current deposits from the early eruption phases preceding caldera collapse. On macroscopic and SEM observations, flat clast faces are elongated parallel to tube vesicles, while transverse surfaces often occur at ~ 45° to vesicle elongation. This peculiar pumice texture provides evidence of high shear stresses related to strong velocity gradients normal to conduit walls, which induced vesiculation and fragmentation of the ascending magma. Either an increasing mass discharge rate without adequate enlargement of a narrow central feeder conduit or a developing fissure-like feeder system related to incipient caldera collapse provided suitable conditions for the generation of plate tube pumice within magma volumes under high shear during the pre-climactic KPT eruption phases. This mechanism implies that the closer to the conduit walls (where the stronger are the velocity gradients) the larger was the proportion of plate vs. conventional (lensoid) juvenile fragments in the ascending gas-pyroclast mixture. Consequently, plate pumice clasts were mainly entrained in the outer portions of the jet and convecting regions of a sustained, Plinian-type, eruption column, as well as in occasional lateral blast currents generated at the vent. As a whole, plate pumice clasts in the peripheral portions of the column were transported at lower altitudes and deposited by fallout or partial collapse closer to the vent relative to lensoid ones

Ag Isotopic Evolution of the Mantle During Accretion: New Constraints from Pd and Ag Metal-Silicate Partitioning

Science.gov (United States)

Righter, K.; Schonbachler, M.

2018-01-01

Decay of (sup 107) Pd to (sup 107) Ag has a half-life of 6.5 times 10 (sup 6) mega-annums. Because these elements are siderophile but also volatile, they offer potential constraints on the timing of core formation as well as volatile addition. Initial modelling has shown that the Ag isotopic composition of the bulk silicate Earth (BSE) can be explained if accretion occurs with late volatile addition. These arguments were tested for sensitivity for pre-cursor Pd/Ag contents, and for a fixed Pd/Ag ratio of the BSE of 0.1. New Ag and Pd partitioning data has allowed a better understanding of the partitioning behavior of Pd and Ag during core formation. The effects of S, C and Si, and the effect of high temperature and pressure has been evaluated. We can now calculate D(Ag) and D(Pd) over the wide range of PT conditions and variable metallic liquid compositions that are known during accretion. We then use this new partitioning information to revisit the Ag isotopic composition of the BSE during accretion.

Geochemical evolution of Ngorongoro Caldera, Northern Tanzania: Implications for crust magma interaction

Science.gov (United States)

Mollel, Godwin F.; Swisher, Carl C.; Feigenson, Mark D.; Carr, Michael J.

2008-07-01

Ngorongoro Caldera is the largest and best-preserved of nine Plio-Pleistocene volcanoes that make-up the Ngorongoro Volcanic Highlands (NVH) complex situated at the southern bifurcation of Gregory Rift, part of the East African Rift system of northern Tanzania. We report here, major and trace element abundances, Sr-Nd-Pb isotope analyses and 40Ar/ 39Ar laser incremental-heating and total fusion ages on lava and tephra sampled from stratigraphic sections exposed within the Ngorongoro Caldera. Major and trace elements measured on samples collected from the Ngorongoro Caldera wall indicate a stratified magma chamber whose silicic top and basaltic bottom was inverted by sequential eruptions. Samples from the lower part of the exposed Ngorongoro Caldera wall are high in silica, alkalis and HFSE (High Field Strength Elements). The Zr, Nb and Hf concentrations are highly correlated with each other and decrease up-section, indicative of the extent of magma evolution. Modeling of major, trace as well as Sr, Nd and Pb isotope data suggests that assimilation fractional crystallization processes were essential in producing the observed geochemical variations. The Sr and Nd isotope ratios from the Ngorongoro samples are widely dispersed ( 87Sr/ 86Sr = 0.70405 to 0.70801, 143Nd/ 144Nd = 0.512205 to 0.512623) and Pb isotope ratios are consistent with previous studies: 206Pb/ 204Pb = 18.73 to 19.37, 207Pb/ 204Pb = 15.64 to 15.69, 208Pb/ 204Pb = 39.52 to 39.55. Although Sr isotopic ratios are similar to Oceanic Island Basalt (OIB), the more radiogenic samples ( 87Sr/ 86Sr > 0.705) from the lower part of the section suggest crust-magma interaction; this is supported by Ce/Pb ratios (Ngorongoro Caldera wall section yield 40Ar/ 39Ar ages of 2.25 ± 0.02 Ma to 2.01 ± 0.02 Ma, constraining a duration of volcanism of the order of ~ 240 kyr. These ages suggest correlation of a normal to reverse geomagnetic polarity transition measured in the Ngorongoro Caldera wall section with the ~ 2

21 CFR 582.2227 - Calcium silicate.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Calcium silicate. 582.2227 Section 582.2227 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Calcium silicate. (a) Product. Calcium silicate. (b) Tolerance. 2 percent and 5 percent. (c) Limitations...

Use of depleted uranium silicate glass to minimize release of radionuclides from spent nuclear fuel waste packages

International Nuclear Information System (INIS)

Forsberg, C.W.

1996-01-01

A Depleted Uranium Silicate Container Backfill System (DUSCOBS) is proposed that would use small, isotopically-depleted uranium silicate glass beads as a backfill material inside repository waste packages containing spent nuclear fuel (SNF). The uranium silicate glass beads would fill the void space inside the package including the coolant channels inside SNF assemblies. Based on preliminary analysis, the following benefits have been identified. DUSCOBS improves repository waste package performance by three mechanisms. First, it reduces the radionuclide releases from SNF when water enters the waste package by creating a local uranium silicate saturated groundwater environment that suppresses (a) the dissolution and/or transformation of uranium dioxide fuel pellets and, hence, (b) the release of radionuclides incorporated into the SNF pellets. Second, the potential for long-term nuclear criticality is reduced by isotopic exchange of enriched uranium in SNF with the depleted uranium (DU) in the glass. Third, the backfill reduces radiation interactions between SNF and the local environment (package and local geology) and thus reduces generation of hydrogen, acids, and other chemicals that degrade the waste package system. Finally, DUSCOBS provides a potential method to dispose of significant quantities of excess DU from uranium enrichment plants at potential economic savings. DUSCOBS is a new concept. Consequently, the concept has not been optimized or demonstrated in laboratory experiments

Density of alkaline magmas at crustal and upper mantle conditions by X-ray absorption

Science.gov (United States)

Seifert, R.; Malfait, W.; Petitgirard, S.; Sanchez-Valle, C.

2011-12-01

Silicate melts are essential components of igneous processes and are directly involved in differentiation processes and heat transfer within the Earth. Studies of the physical properties of magmas (e.g., density, viscosity, conductivity, etc) are however challenging and experimental data at geologically relevant pressure and temperature conditions remain scarce. For example, there is virtually no data on the density at high pressure of alkaline magmas (e.g., phonolites) typically found in continental rift zone settings. We present in situ density measurements of alkaline magmas at crustal and upper mantle conditions using synchrotron X-ray absorption. Measurements were conducted on ID27 beamline at ESRF using a panoramic Paris-Edinburgh Press (PE Press). The starting material is a synthetic haplo-phonolite glass similar in composition to the Plateau flood phonolites from the Kenya rift [1]. The glass was synthesized at 1673 K and 2.0 GPa in a piston-cylinder apparatus at ETH Zurich and characterized using EPMA, FTIR and density measurements. The sample contains less than 200 ppm water and is free of CO2. Single-crystal diamond cylinders (Øin = 0.5 mm, height = 1 mm) were used as sample containers and placed in an assembly formed by hBN spacers, a graphite heater and a boron epoxy gasket [2]. The density was determined as a function of pressure (1.0 to 3.1 GPa) and temperature (1630-1860 K) from the X-ray absorption contrast at 20 keV between the sample and the diamond capsule. The molten state of the sample during the data collection was confirmed by X-ray diffraction measurements. Pressure and temperature were determined simultaneously from the equation of state of hBN and platinum using the the double isochor method [3].The results are combined with available density data at room conditions to derive the first experimental equation of state (EOS) of phonolitic liquids at crustal and upper mantle conditions. We will compare our results with recent reports of the

Duration of a Magma Ocean and Subsequent Mantle Overturn in Mars: Evidence from Nakhlites

Science.gov (United States)

Debaille, V.; Brandon, A. D.; Yin, Q.-Z.; Jacobsen, B.

2008-01-01

It is now generally accepted that the heat produced by accretion, short-lived radioactive elements such as Al-26, and gravitational energy from core formation was sufficient to at least partially melt the silicate portions of terrestrial planets resulting in a global-scale magma ocean. More particularly, in Mars, the geochemical signatures displayed by shergottites, are likely inherited from the crystallization of this magma ocean. Using the short-lived chronometer Sm-146 - Nd-142 (t(sup 1/2) = 103 Myr), the duration of the Martian magma ocean (MMO) has been evaluated to being less than 40 Myr, while recent and more precise ND-142/ND-144 data were used to evaluate the longevity of the MMO to approximately 100 Myr after the solar system formation. In addition, it has been proposed that the end of the crystallization of the MMO may have triggered a mantle overturn, as a result of a density gradient in the cumulate layers crystallized at different levels. Dating the mantle overturn could hence provide additional constraint on the duration of the MMO. Among SNC meteorites, nakhlites are characterized by high epsilon W-182 of approximately +3 and an epsilon Nd-142 similar to depleted shergottites of +0.6-0.9. It has hence been proposed that the source of nakhlites was established very early in Mars history (approximately 8-10 Myr). However, the times recorded in HF-182-W-182 isotope system, i.e. when 182Hf became effectively extinct (approximately 50 Myr after solar system formation) are less than closure times recorded in the Sm-146-Nd-142 isotope system (with a full coverage of approximately 500 Myr after solar system formation). This could result in decoupling between the present-day measured epsilon W-182 and epsilon Nd-142 as the SM-146 may have recorded later differentiation events in epsilon ND-142 not observed in epsilon W-182 values. With these potential complexities in short-lived chronological data for SNC's in mind, new Hf-176/Hf-177, Nd-143/Nd-144 and Nd

21 CFR 182.2227 - Calcium silicate.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Calcium silicate. 182.2227 Section 182.2227 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR... Calcium silicate. (a) Product. Calcium silicate. (b) Tolerance. 2 percent and 5 percent. (c) Limitations...

Biological and therapeutic effects of ortho-silicic acid and some ortho-silicic acid-releasing compounds: New perspectives for therapy

Directory of Open Access Journals (Sweden)

Jurkić Lela Munjas

2013-01-01

Full Text Available Abstract Silicon (Si is the most abundant element present in the Earth's crust besides oxygen. However, the exact biological roles of silicon remain unknown. Moreover, the ortho-silicic acid (H4SiO4, as a major form of bioavailable silicon for both humans and animals, has not been given adequate attention so far. Silicon has already been associated with bone mineralization, collagen synthesis, skin, hair and nails health atherosclerosis, Alzheimer disease, immune system enhancement, and with some other disorders or pharmacological effects. Beside the ortho-silicic acid and its stabilized formulations such as choline chloride-stabilized ortho-silicic acid and sodium or potassium silicates (e.g. M2SiO3; M= Na,K, the most important sources that release ortho-silicic acid as a bioavailable form of silicon are: colloidal silicic acid (hydrated silica gel, silica gel (amorphous silicon dioxide, and zeolites. Although all these compounds are characterized by substantial water insolubility, they release small, but significant, equilibrium concentration of ortho-silicic acid (H4SiO4 in contact with water and physiological fluids. Even though certain pharmacological effects of these compounds might be attributed to specific structural characteristics that result in profound adsorption and absorption properties, they all exhibit similar pharmacological profiles readily comparable to ortho-silicic acid effects. The most unusual ortho-silicic acid-releasing agents are certain types of zeolites, a class of aluminosilicates with well described ion(cation-exchange properties. Numerous biological activities of some types of zeolites documented so far might probably be attributable to the ortho-silicic acid-releasing property. In this review, we therefore discuss biological and potential therapeutic effects of ortho-silicic acid and ortho-silicic acid -releasing silicon compounds as its major natural sources.

Contrasting sodic and mildly potassic magma differentiation lineages at The Pleaides volcanic complex, northern Victoria Land, Antarctica

Science.gov (United States)

Kim, J.; Park, J. W.; Lee, J.; Kyle, P. R.; Lee, M. J.

2017-12-01

The magma evolution of The Pleiades, a Quaternary alkaline volcanic complex in northern Victoria Land, Antarctica, is investigated using major and trace elements, and Sr, Nd and Pb isotopic data. The volcanic rocks can be subdivided into two distinct magmatic lineages based on petrography and whole-rock compositions: (1) a sodic silica-undersaturated alkaline lineage with abundant kaersutite phenocrysts, and (2) a mildly-potassic and mildly-alkaline, nearly silica-saturated lineage containing olivine but not kaersutite. The basanite and trachybasalt of both lineages exhibit similar degrees of negative K anomalies, moderately steep rare earth element patterns, and elevated trace element ratios such as Ce/Pb (> 20) and Nb/U (> 38), suggesting their primary magmas were generated by low degree (≤3%) of partial melting of amphibole and garnet-bearing mantle sources. The sodic lineage is characterized by elevated 206Pb/204Pb (>19.5) ratios and narrow ranges of 87Sr/86Sr (0.70313-0.70327) and 143Nd/144Nd (0.51289-0.51290) ratios consistent with a significant HIMU component typical of Neogene volcanic rocks in Antarctica. The mafic rocks of the potassic lineage have isotopic compositions similar to those of the sodic lineage, however the evolved lavas in the lineage have higher 87Sr/86Sr (> 0.7035) and lower 143Nd/144Nd (< 0.51285) and 206Pb/204Pb (< 19.3) ratios than the mafic rocks, suggesting significant amounts of crustal contamination. The pressure-temperature paths estimated by clinopyroxene-liquid thermobarometry are similar in each lineage. The mafic magmas were emplaced at Moho depths ( 1.2 GPa) and the evolved magmas pooled at middle-crustal depths ( 0.7 GPa). Mass-balance calculations based on whole-rock and mineral compositions show that kaersutite fractionation has played a major role in magma differentiation of the sodic lineage whereas the compositional variations of the potassic lineage can be ascribed to fractionation of a kaersutite-free mineral

Iron Redox Systematics of Martian Magmas

Science.gov (United States)

Righter, K.; Danielson, L.; Martin, A.; Pando, K.; Sutton, S.; Newville, M.

2011-01-01

Martian magmas are known to be FeO-rich and the dominant FeO-bearing mineral at many sites visited by the Mars Exploration rovers (MER) is magnetite [1]. Morris et al. [1] propose that the magnetite appears to be igneous in origin, rather than of secondary origin. However, magnetite is not typically found in experimental studies of martian magmatic rocks [2,3]. Magnetite stability in terrestrial magmas is well understood, as are the stability of FeO and Fe2O3 in terrestrial magmas [4,5]. In order to better understand the variation of FeO and Fe2O3, and the stability of magnetite (and other FeO-bearing phases) in martian magmas we have undertaken an experimental study with two emphases. First we document the stability of magnetite with temperature and fO2 in a shergottite bulk composition. Second, we determine the FeO and Fe2O3 contents of the same shergottite bulk composition at 1 bar and variable fO2 at 1250 C, and at variable pressure. These two goals will help define not only magnetite stability, but pyroxene-melt equilibria that are also dependent upon fO2.

Temporal constraints on magma generation and differentiation in a continental volcano: Buckland, eastern Australia

Science.gov (United States)

Crossingham, Tracey J.; Ubide, Teresa; Vasconcelos, Paulo M.; Knesel, Kurt M.; Mallmann, Guilherme

2018-03-01

The eastern margin of the Australian continent hosts a large number of Cenozoic intraplate volcanoes along a 2000 km long track. Here, we study mafic lavas from the Buckland volcano, Queensland, located in the northern (older) segment of this track, to assess magma generation and differentiation through time. The rocks are aphanitic to microporphyritic basalts, trachy-basalts and basanites. Incompatible element geochemistry together with Sr-Nd-Pb isotope ratios indicate that magmas formed from an enriched mantle I (EMI)-like garnet-bearing source with variable degrees of crustal contamination. Whole rock elemental variations suggest fractionation of olivine, plagioclase, clinopyroxene and/or magnetite. There is no petrographic or geochemical evidence of magma mixing in the studied rocks (e.g., lack of recycled minerals), suggesting a relatively quick ascent from the source to the surface without major storage at shallow levels. 40Ar/39Ar geochronology reveals two stages of volcanism: 30.3 ± 0.1 Ma and 27.4 ± 0.2 Ma. The Old Buckland (30.3 ± 0.1 Ma) melts have negative K anomalies, and incompatible element ratios suggest the occurrence of residual hydrous minerals in a metasomatised mantle source. We therefore infer that at the onset of volcanism, deep-mantle-derived magmas interacted with metasomatised sub-continental lithospheric mantle (SCLM). Major and trace element data, clinopyroxene thermobarometry and thermodynamic modelling indicate magma evolution by assimilation and fractional crystallisation (AFC) during ascent through the crust. Following a hiatus in volcanic activity of 2.5 Ma, eruption of Young Buckland (27.4 ± 0.2 Ma) lavas marked a shift towards more alkaline compositions. Trace element compositions indicate lower degrees of partial melting and a lack of interaction with metasomatic components. Young Buckland lavas become progressively more SiO2-saturated up stratigraphy, suggesting an increase in the degree of partial melting with time. Young

Insights into the emplacement of upper-crustal plutons and their relationship to large silicic calderas, from field relationships, geochronology, and zircon trace element geochemistry in the Stillwater – Clan Alpine caldera complex, western Nevada, USA

Science.gov (United States)

Colgan, Joseph P.; John, David A.; Henry, Christopher D.; Watts, Kathryn E.

2018-01-01

Geologic mapping, new U-Pb zircon ages, and new and published 40Ar/39Ar sanidine ages document the timing and extent of Oligocene magmatism in the southern Stillwater Range and Clan Alpine Mountains of western Nevada, where Miocene extension has exposed at least six nested silicic calderas and underlying granitic plutons to crustal depths locally ≥ 9 km. Both caldera-forming rhyolitic tuffs and underlying plutons were emplaced in two episodes, one from about 30.4–28.2 Ma that included the Deep Canyon, Job Canyon, and Campbell Creek calderas and underlying plutons, and one from about 25.3–24.8 Ma that included the Louderback Mountains, Poco Canyon, and Elevenmile Canyon calderas and underlying plutons. In these two 1–2 m.y. periods, almost the entire Mesozoic upper crust was replaced by Oligocene intrusive and extrusive rocks to depths ≥ 9 km over an estimated total area of ~ 1500 km2 (pre-extension). Zircon trace element geochemistry indicates that some plutonic rock can be solidified residual magma from the tuff eruptions. Most plutons are not solidified residual magma, although they directly underlie calderas and were emplaced along the same structures shortly after to as much as one million years after caldera formation. Magma chambers and plutons grew by floor subsidence accommodated by downward transfer of country rocks. If other Great Basin calderas are similar, the dense concentration of shallowly exposed calderas in central Nevada is underlain by a complexly zoned mid-Cenozoic batholith assembled in discrete pulses that coincided with formation of large silicic calderas up to 2500–5000 km3.

Bayesian inversion of data from effusive volcanic eruptions using physics-based models: Application to Mount St. Helens 2004--2008

Science.gov (United States)

Anderson, Kyle; Segall, Paul

2013-01-01

Physics-based models of volcanic eruptions can directly link magmatic processes with diverse, time-varying geophysical observations, and when used in an inverse procedure make it possible to bring all available information to bear on estimating properties of the volcanic system. We develop a technique for inverting geodetic, extrusive flux, and other types of data using a physics-based model of an effusive silicic volcanic eruption to estimate the geometry, pressure, depth, and volatile content of a magma chamber, and properties of the conduit linking the chamber to the surface. A Bayesian inverse formulation makes it possible to easily incorporate independent information into the inversion, such as petrologic estimates of melt water content, and yields probabilistic estimates for model parameters and other properties of the volcano. Probability distributions are sampled using a Markov-Chain Monte Carlo algorithm. We apply the technique using GPS and extrusion data from the 2004–2008 eruption of Mount St. Helens. In contrast to more traditional inversions such as those involving geodetic data alone in combination with kinematic forward models, this technique is able to provide constraint on properties of the magma, including its volatile content, and on the absolute volume and pressure of the magma chamber. Results suggest a large chamber of >40 km3 with a centroid depth of 11–18 km and a dissolved water content at the top of the chamber of 2.6–4.9 wt%.

Oxidation of volatile organic vapours in air by solid potassium permanganate

NARCIS (Netherlands)

Mahmoodlu, M.G.; Hartog, N.; Hassanizadeh, S.M.; Raoof, A.

2013-01-01

Volatile organic compounds (VOCs) may frequently contaminate groundwater and pose threat to human health when migrating into the unsaturated soil zone and upward to the indoor air. The kinetic of chemical oxidation has been investigated widely for dissolved VOCs in the saturated zone. But, so far

Measurements of the Activity of dissolved H2O in an Andesite Melt

Science.gov (United States)

Moore, G. M.; Touran, J. P.; Pu, X.; Kelley, K. A.; Cottrell, E.; Ghiorso, M. S.

2016-12-01

The large effect of dissolved H2O on the physical and chemical nature of silicate melts, and its role in driving volcanism, is well known and underscores the importance of this volatile component. A complete understanding of the chemical behavior of dissolved H2O in silicate melts requires the quantification of its thermodynamic activity as a function of pressure, temperature, and melt composition, particularly at low H2O contents (i.e. at under-saturated conditions). Knowledge of the activity of H2O in silicate melts at H2O-undersaturated conditions will improve our understanding of hydrous phase equilibria, as well as our models of physical melt properties. Measurement of the activity of any silicate melt component, much less that of a volatile component such as H2O, is a difficult experimental task however. By using a modified double capsule design (Matjuschkin et al, 2015) to control oxygen fugacity in piston cylinder experiments, along with high precision X-ray absorption techniques (XANES) to measure iron oxidation state in silicate glasses (Cottrell et al, 2009), we are able to constrain the H2O activity in silicate melts at under-saturated conditions. Preliminary results on an andesite melt with low H2O content (3 wt%) have been shown (Moore et al, 2016) to match predicted H2O activity values calculated using the H2O equation of state of Duan and Zhang (1996) and the H2O solubility model of Ghiorso and Gualda (2015). More recent results on the same andesite melt containing approximately 5 wt% H2O however show a large negative deviation from the predicted values. Reversal experiments involving an oxidized starting material are ongoing, as well as further characterization of the samples to detect the presence of possible contaminants that would induce reduction of the melt beyond that related to the H2O activity (e.g. graphite contamination).

Magma Dynamics in Dome-Building Volcanoes

Science.gov (United States)

Kendrick, J. E.; Lavallée, Y.; Hornby, A. J.; Schaefer, L. N.; Oommen, T.; Di Toro, G.; Hirose, T.

2014-12-01

The frequent and, as yet, unpredictable transition from effusive to explosive volcanic behaviour is common to active composite volcanoes, yet our understanding of the processes which control this evolution is poor. The rheology of magma, dictated by its composition, porosity and crystal content, is integral to eruption behaviour and during ascent magma behaves in an increasingly rock-like manner. This behaviour, on short timescales in the upper conduit, provides exceptionally dynamic conditions that favour strain localisation and failure. Seismicity released by this process can be mimicked by damage accumulation that releases acoustic signals on the laboratory scale, showing that the failure of magma is intrinsically strain-rate dependent. This character aids the development of shear zones in the conduit, which commonly fracture seismogenically, producing fault surfaces that control the last hundreds of meters of ascent by frictional slip. High-velocity rotary shear (HVR) experiments demonstrate that at ambient temperatures, gouge behaves according to Byerlee's rule at low slip velocities. At rock-rock interfaces, mechanical work induces comminution of asperities and heating which, if sufficient, may induce melting and formation of pseudotachylyte. The viscosity of the melt, so generated, controls the subsequent lubrication or resistance to slip along the fault plane thanks to non-Newtonian suspension rheology. The bulk composition, mineralogy and glass content of the magma all influence frictional behaviour, which supersedes buoyancy as the controlling factor in magma ascent. In the conduit of dome-building volcanoes, the fracture and slip processes are further complicated: slip-rate along the conduit margin fluctuates. The shear-thinning frictional melt yields a tendency for extremely unstable slip thanks to its pivotal position with regard to the glass transition. This thermo-kinetic transition bestows the viscoelastic melt with the ability to either flow or

Two-phase flow in volatile oil reservoir using two-phase pseudo-pressure well test method

Energy Technology Data Exchange (ETDEWEB)

Sharifi, M.; Ahmadi, M. [Calgary Univ., AB (Canada)

2009-09-15

A study was conducted to better understand the behaviour of volatile oil reservoirs. Retrograde condensation occurs in gas-condensate reservoirs when the flowing bottomhole pressure (BHP) lowers below the dewpoint pressure, thus creating 4 regions in the reservoir with different liquid saturations. Similarly, when the BHP of volatile oil reservoirs falls below the bubblepoint pressure, two phases are created in the region around the wellbore, and a single phase (oil) appears in regions away from the well. In turn, higher gas saturation causes the oil relative permeability to decrease towards the near-wellbore region. Reservoir compositional simulations were used in this study to predict the fluid behaviour below the bubblepoint. The flowing bottomhole pressure was then exported to a well test package to diagnose the occurrence of different mobility regions. The study also investigated the use of a two-phase pseudo-pressure method on volatile and highly volatile oil reservoirs. It was concluded that this method can successfully predict the true permeability and mechanical skin. It can also distinguish between mechanical skin and condensate bank skin. As such, the two-phase pseudo-pressure method is particularly useful for developing after-drilling well treatment and enhanced oil recovery process designs. However, accurate relative permeability and PVT data must be available for reliable interpretation of the well test in volatile oil reservoirs. 18 refs., 3 tabs., 9 figs.

Cost-benefit analyses for the development of magma power

International Nuclear Information System (INIS)

Haraden, John

1992-01-01

Magma power is the potential generation of electricity from shallow magma bodies in the crust of the Earth. Considerable uncertainty still surrounds the development of magma power, but most of that uncertainty may be eliminated by drilling the first deep magma well. The uncertainty presents no serious impediments to the private drilling of the well. For reasons unrelated to the uncertainty, there may be no private drilling and there may be justification for public drilling. In this paper, we present cost-benefit analyses for private and public drilling of the well. Both analyses indicate there is incentive for drilling. (Author)

NON-AUTOCLAVE SILICATE BRICK

Directory of Open Access Journals (Sweden)

V. N. Yaglov

2015-01-01

Full Text Available The paper proposes a technology for obtaining bricks on the basis of lime-silica mixtures where chemical interactions are practically completely realized in dispersive state at the stage of preparation of binding contact maturing and raw mixture as a whole. The role of forming operation (moulding is changed in principle because in this case conversion of dispersive system into a rock-like solid occurs and due to this the solid obtains complete water-resistance in contact with water immediately after forming operation. Theoretical basis for the developed technology is capability of silicate dispersive substances (hydrated calcium silicate to transit in non-stable state, to form a rock-like water-resistant solid in the moment of mechanical load application during forming process. Specific feature of the proposed method is an exclusion of additional operations for autoclaving of products from the process of obtaining a silicate brick.Synthetic hydrated calcium silicate in contrast to natural ones are more uniform in composition and structure, they contain less impurities and they are characterized by dispersive composition and due to the mentioned advantages they find wider practical application. Contact-condensation binders permit to manipulate product properties on their basis and ensure maximum correspondence to the requirements of the concrete application. Raw material sources for obtaining synthetic hydrated calcium silicates are practically un-limited because calcium-silicon containing substances are found as in various technogenic wastes so in natural compounds as well. So the problem for obtaining hydrated calcium silicates having contact-condensation ability for structure formation becomes more and more actual one. This transition is considered as dependent principally on arrangement rate of substance particles which determined the level of its instability.

Mobility of plume-derived volcanogenic elements in meteoric water at Nyiragongo volcano (Congo) inferred from the chemical composition of single rainfall events

Science.gov (United States)

Liotta, Marcello; Shamavu, Patient; Scaglione, Sarah; D'Alessandro, Walter; Bobrowski, Nicole; Bruno Giuffrida, Giovanni; Tedesco, Dario; Calabrese, Sergio

2017-11-01

The chemical composition of single rainfall events was investigated at Nyiragongo volcano (Democratic Republic of Congo) with the aim of determining the relative contributions of plume-derived elements. The different locations of the sampling sites allowed both plume-affected samples (hereafter referred to as ;fumigated samples;) and samples representative of the local background to be collected. The chemical composition of the local background reflects the peculiar geographic features of the area, being influenced by biomass burning, geogenic dust, and biological activity. Conversely, fumigated samples contain large amounts of volcanogenic elements that can be clearly distinguished from the local background. These elements are released into the atmosphere from the persistently boiling lava lake of the Nyiragongo crater and from the neonate lava lake of Nyamulagira. These emissions result in a volcanic plume that includes solid particles, acidic droplets, and gaseous species. The chemical signature of the volcanic emissions appears in falling raindrops as they interact with the plume. HCl and HBr readily dissolve in water, and so their ratio in rain samples reflects that of the volcanic plume. The transport of HF is mediated by the large amount of silicate particles generated at the magma-air interface. SO2 is partially converted into SO42- that dissolves in water. The refractory elements dissolved in rain samples derive from the dissolution of silicate particles, and most of them (Al, Mg, Ca, and Sr) are present at exactly the same molar ratios as in the rocks. In contrast, elements such as Na, K, Rb, Cu, and Pb are enriched relative to the whole-rock composition, suggesting that they are volatilized during magma degassing. After correcting for the dissolution of silicate particles, we can define that the volatility of the elements decreases in the following order: Pb ≫ Rb > K > Na. This finding, which is the first for a volcanic plume, is consistent with

A model of sulphur solubility for hydrous mafic melts: application to the determination of magmatic fluid compositions of Italian volcanoes

Directory of Open Access Journals (Sweden)

M. Pichavant

2005-06-01

Full Text Available We present an empirical model of sulphur solubility that allows us to calculate f S2 if P, T, fO2 and the melt composition, including H2O and S, are known. The model is calibrated against three main experimental data bases consisting in both dry and hydrous silicate melts. Its prime goal is to calculate the f S2 of hydrous basalts that currently lack experimental constraints of their sulphur solubility behaviour. Application of the model to Stromboli, Vesuvius, Vulcano and Etna eruptive products shows that the primitive magmas found at these volcanoes record f S2 in the range 0.1-1 bar. In contrast, at all volcanoes the magmatic evolution is marked by dramatic variations in f S2 that spreads over up to 9 orders of magnitude. The f S2 can either increase during differentiation or decrease during decompression to shallow reservoirs, and seems to be related to closed versus open conduit conditions, respectively. The calculated f S2 shows that the Italian magmas are undersaturated in a FeS melt, except during closed conduit conditions, in which case differentiation may eventually reach conditions of sulphide melt saturation. The knowledge of f S2, fO2 and fH2O allows us to calculate the fluid phase composition coexisting with magmas at depth in the C-O-H-S system. Calculated fluids show a wide range in composition, with CO2 mole fractions of up to 0.97. Except at shallow levels, the fluid phase is generally dominated by CO2 and H2O species, the mole fractions of SO2 and H2S rarely exceeding 0.05 each. The comparison between calculated fluid compositions and volcanic gases shows that such an approach should provide constraints on both the depth and mode of degassing, as well as on the amount of free fluid in magma reservoirs. Under the assumption of a single step separation of the gas phase in a closed-system condition, the application to Stromboli and Etna suggests that the main reservoirs feeding the eruptions and persistent

Regularities in Low-Temperature Phosphatization of Silicates

Science.gov (United States)

Savenko, A. V.

2018-01-01

The regularities in low-temperature phosphatization of silicates are defined from long-term experiments on the interaction between different silicate minerals and phosphate-bearing solutions in a wide range of medium acidity. It is shown that the parameters of the reaction of phosphatization of hornblende, orthoclase, and labradorite have the same values as for clayey minerals (kaolinite and montmorillonite). This effect may appear, if phosphotization proceeds, not after silicate minerals with a different structure and composition, but after a secondary silicate phase formed upon interaction between silicates and water and stable in a certain pH range. Variation in the parameters of the reaction of phosphatization at pH ≈ 1.8 is due to the stability of the silicate phase different from that at higher pH values.

Magma paths at Piton de la Fournaise Volcano

OpenAIRE

Michon , Laurent; Ferrazzini , Valérie; Di Muro , Andrea

2016-01-01

International audience; Several patterns of magma paths have been proposed since the 1980s for Piton de la Fournaise volcano. Given the significant differences, which are presented here, we propose a reappraisal of the magma intrusion paths using a 17-years-long database of volcano-tectonic seismic events and a detailed mapping of the scoria cones. At the edifice scale, the magma propagates along two N120 trending rift zones. They are wide, linear, spotted by small to large scoria cones and r...

Orientation of the eruption fissures controlled by a shallow magma chamber in Miyakejima

Directory of Open Access Journals (Sweden)

Nobuo Geshi

2016-11-01

Full Text Available Orientation of the eruption fissures and composition of the lavas of the Miyakejima volcano indicate tectonic influence of a shallow magma chamber on the distribution of eruption fissures. We examined the distributions and magmatic compositions of 23 fissures that formed within the last 2800 years, based on a field survey and a new dataset of 14C ages. The dominant orientation of the eruption fissures in the central portion of the volcano was found to be NE-SW, which is perpendicular to the direction of regional maximum horizontal compressive stress (σHmax. Magmas that show evidences of magma mixing between basaltic and andesitic magmas erupted mainly from the eruption fissures with a higher offset angle from the regional σHmax direction. The presence of a shallow dike-shaped magma chamber controls the distribution of the eruption fissures. The injection of basaltic magma into the shallow andesitic magma chamber caused the temporal rise of internal magmatic pressure in the shallow magma chamber. Dikes extending from the andesitic magma chamber intrude along the local compressive stress field which is generated by the internal excess pressure of the andesitic magma chamber. As the result, the eruption fissures trend parallel to the elongation direction of the shallow magma chamber. Injection of basaltic magma into the shallow andesitic magma chamber caused the magma mixing. Some basaltic dikes from the deep-seated magma chamber reach the ground surface without intersection with the andesitic magma chamber. The patterns of the eruption fissures can be modified in the future as was observed in the case of the destruction of the shallow magma chamber during the 2000 AD eruption.

Degassing of CO2, SO2, and H2S associated with the 2009 eruption of Redoubt Volcano, Alaska

Science.gov (United States)

Werner, Cynthia; Kelly, Peter J.; Doukas, Michael; Lopez, Taryn; Pfeffer, Melissa; McGimsey, Robert; Neal, Christina

2013-06-01

The 2009 eruption of Redoubt Volcano, Alaska was particularly well monitored for volcanic gas emissions. We report 35 airborne measurements of CO2, SO2, and H2S emission rates that span from October 2008 to August 2010. The magmatic system degassed primarily as a closed system although minor amounts of open system degassing were observed in the 6 months prior to eruption on March 15, 2009 and over 1 year following cessation of dome extrusion. Only 14% of the total CO2 was emitted prior to eruption even though high emissions rates (between 3630 and 9020 t/d) were observed in the final 6 weeks preceding the eruption. A minor amount of the total SO2 was observed prior to eruption (4%), which was consistent with the low emission rates at that time (up to 180 t/d). The amount of the gas emitted during the explosive and dome growth period (March 15-July 1, 2009) was 59 and 66% of the total CO2 and SO2, respectively. Maximum emission rates were 33,110 t/d CO2, 16,650 t/d SO2, and 1230 t/d H2S. Post-eruptive passive degassing was responsible for 27 and 30% of the total CO2 and SO2, respectively. SO2 made up on average 92% of the total sulfur degassing throughout the eruption. Magmas were vapor saturated with a C- and S-rich volatile phase, and regardless of composition, the magmas appear to be buffered by a volatile composition with a molar CO2/SO2 ratio of ~ 2.4. Primary volatile contents calculated from degassing and erupted magma volumes range from 0.9 to 2.1 wt.% CO2 and 0.27-0.56 wt.% S; whole-rock normalized values are slightly lower (0.8-1.7 wt.% CO2 and 0.22-0.47 wt.% S) and are similar to what was calculated for the 1989-90 eruption of Redoubt. Such contents argue that primary arc magmas are rich in CO2 and S. Similar trends between volumes of estimated degassed magma and observed erupted magma during the eruptive period point to primary volatile contents of 1.25 wt.% CO2 and 0.35 wt.% S. Assuming these values, up to 30% additional unerupted magma degassed in the

DUSCOBS - a depleted-uranium silicate backfill for transport, storage, and disposal of spent nuclear fuel

International Nuclear Information System (INIS)

Forsberg, C.W.; Pope, R.B.; Ashline, R.C.; DeHart, M.D.; Childs, K.W.; Tang, J.S.

1995-01-01

A Depleted Uranium Silicate COntainer Backfill System (DUSCOBS) is proposed that would use small, isotopically-depleted uranium silicate glass beads as a backfill material inside storage, transport, and repository waste packages containing spent nuclear fuel (SNF). The uranium silicate glass beads would fill all void space inside the package including the coolant channels inside SNF assemblies. Based on preliminary analysis, the following benefits have been identified. DUSCOBS improves repository waste package performance by three mechanisms. First, it reduces the radionuclide releases from SNF when water enters the waste package by creating a local uranium silicate saturated groundwater environment that suppresses (1) the dissolution and/or transformation of uranium dioxide fuel pellets and, hence, (2) the release of radionuclides incorporated into the SNF pellets. Second, the potential for long-term nuclear criticality is reduced by isotopic exchange of enriched uranium in SNF with the depleted uranium (DU) in the glass. Third, the backfill reduces radiation interactions between SNF and the local environment (package and local geology) and thus reduces generation of hydrogen, acids, and other chemicals that degrade the waste package system. In addition, the DUSCOBS improves the integrity of the package by acting as a packing material and ensures criticality control for the package during SNF storage and transport. Finally, DUSCOBS provides a potential method to dispose of significant quantities of excess DU from uranium enrichment plants at potential economic savings. DUSCOBS is a new concept. Consequently, the concept has not been optimized or demonstrated in laboratory experiments

The Surtsey Magma Series.

Science.gov (United States)

Schipper, C Ian; Jakobsson, Sveinn P; White, James D L; Michael Palin, J; Bush-Marcinowski, Tim

2015-06-26

The volcanic island of Surtsey (Vestmannaeyjar, Iceland) is the product of a 3.5-year-long eruption that began in November 1963. Observations of magma-water interaction during pyroclastic episodes made Surtsey the type example of shallow-to-emergent phreatomagmatic eruptions. Here, in part to mark the 50(th) anniversary of this canonical eruption, we present previously unpublished major-element whole-rock compositions, and new major and trace-element compositions of sideromelane glasses in tephra collected by observers and retrieved from the 1979 drill core. Compositions became progressively more primitive as the eruption progressed, with abrupt changes corresponding to shifts between the eruption's four edifices. Trace-element ratios indicate that the chemical variation is best explained by mixing of different proportions of depleted ridge-like basalt, with ponded, enriched alkalic basalt similar to that of Iceland's Eastern Volcanic Zone; however, the systematic offset of Surtsey compositions to lower Nb/Zr than other Vestmannaeyjar lavas indicates that these mixing end members are as-yet poorly contained by compositions in the literature. As the southwestern-most volcano in the Vestmannaeyjar, the geochemistry of the Surtsey Magma Series exemplifies processes occurring within ephemeral magma bodies on the extreme leading edge of a propagating off-axis rift in the vicinity of the Iceland plume.

The melt inclusion record from the rhyolitic Kos Plateau Tuff (Aegean Arc)

Science.gov (United States)

Bachmann, Olivier; Wallace, Paul J.; Bourquin, Julie

2010-02-01

The >60 km3 rhyolitic Kos Plateau Tuff provides an exceptional probe into the behavior of volatile components in highly evolved arc magmas: it is crystal-rich (30-40 vol% crystals), was rapidly quenched by the explosive eruptive process, and contains abundant homogeneous melt inclusions in large quartz crystals. Several methods for measuring major, trace and volatile element concentrations (SIMS, FTIR, Raman spectroscopy, electron microprobe, LA-ICPMS) were applied to these melt inclusions. We found a ~2 wt% range of H2O contents (4.5-6.5 wt% H2O, measured independently by SIMS, FTIR, and Raman spectroscopy) and relatively low CO2 concentrations (15-140 ppm measured by FTIR, with most analyses <100 ppm). No obvious correlations between H2O, CO2, major and trace elements are observed. These observations require a complex, protracted magma evolution in the upper crust that included: (1) vapor-saturated crystallization in a chamber located between 1.5 and 2.5 kb pressure, (2) closed-system degassing (with up to 10 vol% exsolved gas) as melts percolated upwards through a vertically extensive mush zone (2-4 km thick), and (3) periodic gas fluxing from subjacent, more mafic and more CO2-rich magma, which is preserved as andesite bands in pumices. These processes can account for the range of observed H2O and CO2 values and the lack of correlation between volatiles and trace elements in the melt inclusions.

Deep magma transport at Kilauea volcano, Hawaii

Science.gov (United States)

Wright, T.L.; Klein, F.W.

2006-01-01

The shallow part of Kilauea's magma system is conceptually well-understood. Long-period and short-period (brittle-failure) earthquake swarms outline a near-vertical magma transport path beneath Kilauea's summit to 20 km depth. A gravity high centered above the magma transport path demonstrates that Kilauea's shallow magma system, established early in the volcano's history, has remained fixed in place. Low seismicity at 4-7 km outlines a storage region from which magma is supplied for eruptions and intrusions. Brittle-failure earthquake swarms shallower than 5 km beneath the rift zones accompany dike emplacement. Sparse earthquakes extend to a decollement at 10-12 km along which the south flank of Kilauea is sliding seaward. This zone below 5 km can sustain aseismic magma transport, consistent with recent tomographic studies. Long-period earthquake clusters deeper than 40 km occur parallel to and offshore of Kilauea's south coast, defining the deepest seismic response to magma transport from the Hawaiian hot spot. A path connecting the shallow and deep long-period earthquakes is defined by mainshock-aftershock locations of brittle-failure earthquakes unique to Kilauea whose hypocenters are deeper than 25 km with magnitudes from 4.4 to 5.2. Separation of deep and shallow long-period clusters occurs as the shallow plumbing moves with the volcanic edifice, while the deep plumbing is centered over the hotspot. Recent GPS data agrees with the volcano-propagation vector from Kauai to Maui, suggesting that Pacific plate motion, azimuth 293.5?? and rate of 7.4 cm/yr, has been constant over Kilauea's lifetime. However, volcano propagation on the island of Hawaii, azimuth 325??, rate 13 cm/yr, requires southwesterly migration of the locus of melting within the broad hotspot. Deep, long-period earthquakes lie west of the extrapolated position of Kilauea backward in time along a plate-motion vector, requiring southwesterly migration of Kilauea's magma source. Assumed ages of 0

Viscosity controlled magma-carbonate interaction: a comparison of Mt. Vesuvius (Italy) and Mt. Merapi (Indonesia).

Science.gov (United States)

Blythe, L. S.; Misiti, V.; Masotta, M.; Taddeucci, J.; Freda, C.; Troll, V. R.; Deegan, F. M.; Jolis, E. M.

2012-04-01

Magma-carbonate interaction is increasingly seen as a viable and extremely important cause of magma contamination, and the generation of a crustally sourced CO2 phase (Goff et al., 2001; Freda et al., 2010). Even though the process is well recognized at certain volcanoes e.g. Popocatépetl, (Mexico); Merapi, (Indonesia); and Colli Albani, (Italy) (Goff et al., 2001; Deegan et al., 2010; Freda et al., 2010), neither the kinetics of carbonate assimilation nor its consequences for controlling the explosivity of eruptions have been constrained. Here we show the results of magma-carbonate interaction experiments conducted at 1200 °C and 0.5 GPa for varying durations (0 s, 60 s, 90 s and 300 s) for the Mt. Merapi (Indonesia) and Mt. Vesuvius (Italy) volcanic systems. We performed experiments using glassy starting materials specific to each volcano (shoshonite for Mt. Vesuvius, basaltic-andesite for Mt. Merapi) with different degrees of hydration (anhydrous vs hydration with ~ 2 wt % water) and using carbonate fragments of local origin; see Deegan et al., (2010) and Jolis et al., (2011). Experimental products include a gas phase (CO2-rich) and two melt phases, one pristine (Ca-normal) and one contaminated (Ca-rich) separated by a 'contamination front' which propagates outwards from the carbonate clast. Vesicles appear to nucleate in the contaminated glass and then migrate into the pristine one. Both contamination front propagation and bubble migration away from the carbonate are slower in anhydrous basaltic-andesite (Merapi anhydrous series) than in hydrated basaltic-andesite and shoshonite (Merapi and Vesuvius hydrated series), suggesting that assimilation speed is strongly controlled by the degree of hydration and the SiO2 content, both of which influence melt viscosity and hence diffusivity. As the carbonate dissolution proceeds in our experiments, initially dissolved and eventually exsolved CO2 builds up in the contaminated Ca-rich melt phase. Once melt volatile

Thermodynamics and Kinetics of Silicate Vaporization

Science.gov (United States)

Jacobson, Nathan S.; Costa, Gustavo C. C.

2015-01-01

Silicates are a common class of materials that are often exposed to high temperatures. The behavior of these materials needs to be understood for applications as high temperature coatings in material science as well as the constituents of lava for geological considerations. The vaporization behavior of these materials is an important aspect of their high temperature behavior and it also provides fundamental thermodynamic data. The application of Knudsen effusion mass spectrometry (KEMS) to silicates is discussed. There are several special considerations for silicates. The first is selection of an appropriate cell material, which is either nearly inert or has well-understood interactions with the silicate. The second consideration is proper measurement of the low vapor pressures. This can be circumvented by using a reducing agent to boost the vapor pressure without changing the solid composition or by working at very high temperatures. The third consideration deals with kinetic barriers to vaporization. The measurement of these barriers, as encompassed in a vaporization coefficient, is discussed. Current measured data of rare earth silicates for high temperature coating applications are discussed. In addition, data on magnesium-iron-silicates (olivine) are presented and discussed.

Partially molten magma ocean model

International Nuclear Information System (INIS)

Shirley, D.N.

1983-01-01

The properties of the lunar crust and upper mantle can be explained if the outer 300-400 km of the moon was initially only partially molten rather than fully molten. The top of the partially molten region contained about 20% melt and decreased to 0% at 300-400 km depth. Nuclei of anorthositic crust formed over localized bodies of magma segregated from the partial melt, then grew peripherally until they coverd the moon. Throughout most of its growth period the anorthosite crust floated on a layer of magma a few km thick. The thickness of this layer is regulated by the opposing forces of loss of material by fractional crystallization and addition of magma from the partial melt below. Concentrations of Sr, Eu, and Sm in pristine ferroan anorthosites are found to be consistent with this model, as are trends for the ferroan anorthosites and Mg-rich suites on a diagram of An in plagioclase vs. mg in mafics. Clustering of Eu, Sr, and mg values found among pristine ferroan anorthosites are predicted by this model

Thermal vesiculation during volcanic eruptions.

Science.gov (United States)

Lavallée, Yan; Dingwell, Donald B; Johnson, Jeffrey B; Cimarelli, Corrado; Hornby, Adrian J; Kendrick, Jackie E; von Aulock, Felix W; Kennedy, Ben M; Andrews, Benjamin J; Wadsworth, Fabian B; Rhodes, Emma; Chigna, Gustavo

2015-12-24

Terrestrial volcanic eruptions are the consequence of magmas ascending to the surface of the Earth. This ascent is driven by buoyancy forces, which are enhanced by bubble nucleation and growth (vesiculation) that reduce the density of magma. The development of vesicularity also greatly reduces the 'strength' of magma, a material parameter controlling fragmentation and thus the explosive potential of the liquid rock. The development of vesicularity in magmas has until now been viewed (both thermodynamically and kinetically) in terms of the pressure dependence of the solubility of water in the magma, and its role in driving gas saturation, exsolution and expansion during decompression. In contrast, the possible effects of the well documented negative temperature dependence of solubility of water in magma has largely been ignored. Recently, petrological constraints have demonstrated that considerable heating of magma may indeed be a common result of the latent heat of crystallization as well as viscous and frictional heating in areas of strain localization. Here we present field and experimental observations of magma vesiculation and fragmentation resulting from heating (rather than decompression). Textural analysis of volcanic ash from Santiaguito volcano in Guatemala reveals the presence of chemically heterogeneous filaments hosting micrometre-scale vesicles. The textures mirror those developed by disequilibrium melting induced via rapid heating during fault friction experiments, demonstrating that friction can generate sufficient heat to induce melting and vesiculation of hydrated silicic magma. Consideration of the experimentally determined temperature and pressure dependence of water solubility in magma reveals that, for many ascent paths, exsolution may be more efficiently achieved by heating than by decompression. We conclude that the thermal path experienced by magma during ascent strongly controls degassing, vesiculation, magma strength and the effusive

Experimental Study of the Partitioning of Siderophile Elements in a Crystallizing Lunar Magma Ocean

Science.gov (United States)

Galenas, M.; Righter, K.; Danielson, L.; Pando, K.; Walker, R. J.

2012-01-01

The distributions of trace elements between the lunar interior and pristine crustal rocks were controlled by the composition of starting materials, lunar core formation, and crystallization of the lunar magma ocean (LMO) [1]. This study focuses on the partitioning of highly siderophile elements (HSE) including Re, Os, Ir, Ru, Pt, Rh, Pd and Au as well as the moderately siderophile elements Mo and W, and the lithophile elements of Hf and Sr. Our experiments also include Ga, which can be slightly siderophile, but is mostly considered to be chalcophile. Partitioning of these elements is not well known at the conditions of a crystallizing LMO. Previous studies of HSE partitioning in silicate systems have yielded highly variable results for differing oxygen fugacity (fO2) and pressure [2-4]. For example, under certain conditions Pt is compatible in clinopy-roxene [2] and Rh and Ru are compatible in olivine [3]. The silicate compositions used for these experiments were nominally basaltic. Ruthenium, Rh, and Pd are incompatible in plagioclase under these conditions[4]. However, this latter study was done at extremely oxidizing conditions and at atmospheric pressure, possibly limiting the applicability for consideration of conditions of a crystallizing LMO. In this study we address the effects of pressure and oxygen fugacity on the crystal/liquid partition coefficients of these trace elements. We are especially interested in the plagioclase/melt partition coefficients so that it may be possible to use reverse modeling to constrain the concentrations of these elements in the lunar mantle through their abundances in pristine crustal rocks.

Thermally-assisted Magma Emplacement Explains Restless Calderas.

Science.gov (United States)

Amoruso, Antonella; Crescentini, Luca; D'Antonio, Massimo; Acocella, Valerio

2017-08-11

Many calderas show repeated unrest over centuries. Though probably induced by magma, this unique behaviour is not understood and its dynamics remains elusive. To better understand these restless calderas, we interpret deformation data and build thermal models of Campi Flegrei caldera, Italy. Campi Flegrei experienced at least 4 major unrest episodes in the last decades. Our results indicate that the inflation and deflation of magmatic sources at the same location explain most deformation, at least since the build-up of the last 1538 AD eruption. However, such a repeated magma emplacement requires a persistently hot crust. Our thermal models show that this repeated emplacement was assisted by the thermal anomaly created by magma that was intruded at shallow depth ~3 ka before the last eruption. This may explain the persistence of the magmatic sources promoting the restless behaviour of the Campi Flegrei caldera; moreover, it explains the crystallization, re-melting and mixing among compositionally distinct magmas recorded in young volcanic rocks. Our model of thermally-assisted unrest may have a wider applicability, possibly explaining also the dynamics of other restless calderas.

Unusual Iron Redox Systematics of Martian Magmas

Science.gov (United States)

Danielson, L.; Righter, K.; Pando, K.; Morris, R. V.; Graff, T.; Agresti, D.; Martin, A.; Sutton, S.; Newville, M.; Lanzirotti, A.

2012-01-01

Martian magmas are known to be FeO-rich and the dominant FeO-bearing mineral at many sites visited by the Mars Exploration rovers (MER) is magnetite. Morris et al. proposed that the magnetite appears to be igneous in origin, rather than of secondary origin. However, magnetite is not typically found in experimental studies of martian magmatic rocks. Magnetite stability in terrestrial magmas is well understood, as are the stabilities of FeO and Fe2O3 in terrestrial magmas. In order to better understand the variation of FeO and Fe2O3, and the stability of magnetite (and other FeO-bearing phases) in martian magmas, we have undertaken an experimental study with two emphases. First, we determine the FeO and Fe2O3 contents of super- and sub-liquidus glasses from a shergottite bulk composition at 1 bar to 4 GPa, and variable fO2. Second, we document the stability of magnetite with temperature and fO2 in a shergottite bulk composition.

«Magma»: as origens de Guimarães Rosa

Directory of Open Access Journals (Sweden)

Luiz Cláudio Vieira de Oliveira

2011-10-01

Full Text Available Resumo: Leitura de Magma, de Guimarães Rosa, com o objetivo de indicar a presença de temas, fragmentos, personagens, expressões e recursos estilísticos ali existentes, em outros textos do autor, cronologicamente posteriores.Palavras-chave: Literatura brasileira; Guimarães Rosa; Magma.Résumé: Lecture de Magma, de Guimarães Rosa, ayant l’objectif de montrer la présence de quelques sujets, fragments, personnages, expressions et traits stylistiques, que y sont présents, et aussi dans autres textes du même auteur, chronologiquement postérieurs.Mots-clés: Littérature brésilienne; Guimarães Rosa; Magma.Keywords: Brazilian literature; Guimarães Rosa; Magma.

Magma ascent, fragmentation and depositional characteristics of "dry" maar volcanoes: Similarities with vent-facies kimberlite deposits

Science.gov (United States)

Berghuijs, Jaap F.; Mattsson, Hannes B.

2013-02-01

Several maar craters within the Lake Natron-Engaruka monogenetic volcanic field (LNE-MVF) of northern Tanzania show compelling evidence for magmatic fragmentation and dry deposition. This is in contradiction of the common belief that most maars are formed through the explosive interaction between ascending magma and ground- or surface water. We here present a detailed study on the eruptive and depositional characteristics of the Loolmurwak and Eledoi maar volcanoes, two of the largest craters in the LNE-MVF, focusing on high-resolution stratigraphy, sedimentology, grain size distribution, pyroclast textures and morphologies, bulk geochemistry and mineral chemistry. At both maars, ejected material has been emplaced by a combination of pyroclastic surges and fallout. Indicators of phreatomagmatic fragmentation and wet deposition, such as impact sags, accretionary lapilli, vesiculated tuffs and plastering against obstacles, are absent in the deposits. Juvenile material predominantly occurs as fluidal-shaped vesicular melt droplets and contains no glass shards produced by the breakage of bubble walls. The Eledoi deposits comprise a large amount of inversely graded beds and lenses, which result from grain flow in a dry depositional environment. Preferential deposition of fine material toward the northern side of its crater can be related to effective wind winnowing in a dry eruption plume. This large variety of observations testifies to the dominance of magmatic fragmentation as well as dry deposition at the Loolmurwak and Eledoi maars, which is in line with what has been found for other structures in the LNE-MVF but contrasts with current ideas on maar formation. We infer that a volatile-rich, olivine melilitic magma was formed by small amounts of partial melting at upper mantle depths. With minimum average ascent rates of 5.3 m s- 1 for Loolmurwak and 26.2 m s- 1 for Eledoi, this magma rapidly moved toward the surface and exsolved a substantial amount of volatiles

Crystalline heterogeneities and instabilities in thermally convecting magma chamber

Science.gov (United States)

Culha, C.; Suckale, J.; Qin, Z.

2016-12-01

A volcanic vent can supply different densities of crystals over an eruption time period. This has been seen in Hawai'i's Kilauea Iki 1959 eruption; however it is not common for all Kilauea or basaltic eruptions. We ask the question: Under what conditions can homogenous magma chamber cultivate crystalline heterogeneities? In some laboratory experiments and numerical simulations, a horizontal variation is observed. The region where crystals reside is identified as a retention zone: convection velocity balances settling velocity. Simulations and experiments that observe retention zones assume crystals do not alter the convection in the fluid. However, a comparison of experiments and simulations of convecting magma with crystals suggest that large crystal volume densities and crystal sizes alter fluid flow considerably. We introduce a computational method that fully resolves the crystalline phase. To simulate basaltic magma chambers in thermal convection, we built a numerical solver of the Navier-Stoke's equation, continuity equation, and energy equation. The modeled magma is assumed to be a viscous, incompressible fluid with a liquid and solid phase. Crystals are spherical, rigid bodies. We create Rayleigh-Taylor instability through a cool top layer and hot bottom layer and update magma density while keeping crystal temperature and size constant. Our method provides a detailed picture of magma chambers, which we compare to other models and experiments to identify when and how crystals alter magma chamber convection. Alterations include stratification, differential settling and instabilities. These characteristics are dependent on viscosity, convection vigor, crystal volume density and crystal characteristics. We reveal that a volumetric crystal density variation may occur over an eruption time period, if right conditions are met to form stratifications and instabilities in magma chambers. These conditions are realistic for Kilauea Iki's 1959 eruption.

Complexities in Shallow Magma Transport at Kilauea (Invited)

Science.gov (United States)

Swanson, D. A.

2013-12-01

The standard model of Kilauea's shallow plumbing system includes magma storage under the caldera and conduits in the southwest rift zone (SWRZ) and the east rift zone (ERZ). As a field geologist, I find that seemingly aberrant locations and trends of some eruptive vents indicate complexities in shallow magma transport not addressed by the standard model. This model is not wrong but instead incomplete, because it does not account for the development of offshoots from the main plumbing. These offshoots supply magma to the surface at places that tell us much about the complicated stress system within the volcano. Perhaps most readily grasped are fissures peripheral to the north and south sides of the caldera. Somehow magma can apparently be injected into caldera-bounding faults from the summit reservoir complex, but the process and pathways are unclear. Of more importance is the presence of fissures with ENE trends on the east side of the caldera, including Kilauea Iki. Is this a rift zone that forms an acute angle with the ERZ? I think there is another explanation: the main part of the ERZ has migrated ~5 km SSE during the past few tens of thousands of years owing to seaward movement of the south flank, but older parts of the rift zone can be reactivated. The fissures east of the caldera have the ERZ trend and may record such reactivation; this interpretation includes the location of the largest eruption (15th century) known from Kilauea. Whether or not this interpretation has validity, the question remains: what changes in the plumbing system allow magma to erupt east of the caldera? The SWRZ can be divided into two sections, the SWRZ proper and the seismically active part (SASWRZ) southeast of the SWRZ. The total width of both sections is ~4 km. The SWRZ might be migrating SSE, as is the ERZ. Fissures in the SWRZ proper trend SW. Fissures in the SASWRZ, however, have ENE trends like that of the ERZ, although, because of en echelon offsets, the fissure zone itself

Geophysical Evidence for the Locations, Shapes and Sizes, and Internal Structures of Magma Chambers beneath Regions of Quaternary Volcanism

Science.gov (United States)

Iyer, H. M.

1984-04-01

at the onset of melting of rocks and to delineate in three dimensions the shape of the partly melted zone. Similarly, decreases in density and electrical resistivity in rocks during melting, can be detected. Seismic refraction and reflection are not yet used extensively in magma chamber studies. In a study, in the Yellowstone region, seismic delays occurring in a fan-shooting configuration and time-term modelling show the presence of an intense molten zone in the upper crust. Deep seismic sounding (a combination of seismic refraction and reflection) and modelling amplitude and velocity changes of diffracted seismic waves from explosions and earthquakes, have enabled mapping of small and large magma chambers beneath many volcanoes in Kamchatka, U.S.S.R. Teleseismic P-wave residuals have been used to model low-velocity bodies, interpreted as magma chambers, in several Quaternary volcanic centres in the U.S.A. The results show that magma chambers with volumes of a few hundred to a few thousand cubic kilometres volume seem to be confined to regions of silicic volcanism. Many of the magma bodies seem to have upper-mantle roots implying that they are not isolated pockets of partial melt, but may be deriving their magma supplies from deeper parental sources. Medium or large crustal magma chambers are absent in the andesitic volcanoes of western United States and the basaltic Kilauea volcano, Hawaii. However, regional velocity models of the Oregon Cascades and Hawaii show evidence for the presence of magma reservoirs in the upper mantle. The transport of magma to the upper crust in these regions probably occurs rapidly through narrow conduits, with transient storage occurring in small chambers of a few cubic kilometres volume. Very little use has been made of the gravity and magnetic maps to model magma chambers. The number of available case histories, though few, indicate that these data can be very useful to give constraints on the density and temperature in magma chambers

Better constraints on the size and volatile content of the Mount St. Helens magma reservoir following the end of the 2004-2008 eruption

Science.gov (United States)

Mastin, L. G.; Lisowski, M.; Beeler, N.; Roeloffs, E.

2008-12-01

The October 2004-January 2008 eruption of Mount St. Helens produced about 93 million cubic meters dense-rock equivalent (DRE) lava at a continuous rate that decreased monotonically from ~6 m3 s-1 to zero over its duration. From late October 2004 through the end of the eruption, continuous GPS stations around the mountain recorded inward deflation at a rate that dropped monotonically below the noise level by early 2007. The geodetic signal is consistent with a volume change Δ Vc of ~16-25M m3 in an ellipsoidal reservoir of volume Vc centered at ~9-14 km depth beneath the crater. Throughout the eruption we used physically based models to extrapolate trends in lava-dome volume and deflation, and to forecast the duration and final erupted volume, Ve, using assumed or geologically constrained values of Vc, average recharge rate R into the reservoir, and compressibilities of magma (Km = ( 1/ρ m )( ∂ ρ m /∂ p )) and of the reservoir (Kc = ( 1/Vc )( ∂ Vc /∂ p )), where ρ m is magma density and p is pressure). Curves that neglected recharge consistently under-predicted both the final duration and volume, while those that assumed a constant recharge rate predicted indefinite duration and volume. The fact that the eruption ended several months after deflation stopped suggests that the long-term average recharge was close to zero, or at least much less than the average eruption rate. The discrepancy between Ve (93M m3) and Δ VC (16-25M m3) can be accounted for by the elastic relation Ve /Δ Vc = ( 1 + Km /Kc ), with Km = 3 - 4 × 10- 10 Pa-1 calculated for reservoir magma with 1- 1.5% bubbles (constrained from gas studies of the erupted lava), and Kc = 1.1 - 1.5 × 10 - 10 Pa-1. Assuming that the pressure drop dp in the reservoir was only slightly greater than the ~5 MPa increase in pressure at the 2004 vent elevation due to growth of the 220-m-high lava dome, the elastic relation Ve = VC dp( Kc + Km ) suggests that the eruption could have been fed by a reservoir

Phosphorus availability in oxidic soils treated with lime and silicate applications

Directory of Open Access Journals (Sweden)

Aline da Silva Sandim

2014-08-01

Full Text Available Based on the assumption that silicate application can raise soil P availability for crops, the aim of this research was to compare the effect of silicate application on soil P desorption with that of liming, in evaluations based on two extractors and plant growth. The experiment was carried out in randomized blocks with four replications, in a 3 × 3 × 5 factorial design, in which three soil types, three P rates, and four soil acidity correctives were evaluated in 180 experimental plots. Trials were performed in a greenhouse using corn plants in 20-dm³ pots. Three P rates (0, 50 and 150 mg dm-3 were applied in the form of powder triple superphosphate and the soil was incubated for 90 days. After this period, soil samples were collected for routine chemical analysis and P content determination by the extraction methods resin, Mehlich-1 and remaining P. Based on the results, acidity correctives were applied at rates calculated for base saturation increased to 70 %, with subsequent incubation for 60 more days, when P content was determined again. The acidity correctives consisted of: dolomitic lime, steelmaking slag, ladle furnace slag, and wollastonite. Therefore, our results showed that slags raised the soil P content more than lime, suggesting a positive correlation between P and Si in soil. Silicon did not affect the extractor choice since both Mehlich-1 and resin had the same behavior regarding extracted P when silicon was applied to the soil. For all evaluated plant parameters, there was significant interaction between P rates and correctives; highest values were obtained with silicate.

Magma Ocean Depth and Oxygen Fugacity in the Early Earth--Implications for Biochemistry.

Science.gov (United States)

Righter, Kevin

2015-09-01

A large class of elements, referred to as the siderophile (iron-loving) elements, in the Earth's mantle can be explained by an early deep magma ocean on the early Earth in which the mantle equilibrated with metallic liquid (core liquid). This stage would have affected the distribution of some of the classic volatile elements that are also essential ingredients for life and biochemistry - H, C, S, and N. Estimates are made of the H, C, S, and N contents of Earth's early mantle after core formation, considering the effects of variable temperature, pressure, oxygen fugacity, and composition on their partitioning. Assessment is made of whether additional, exogenous, sources are required to explain the observed mantle concentrations, and areas are identified where additional data and experimentation would lead to an improved understanding of this phase of Earth's history.

Encapsulation of TRISO particle fuel in durable soda-lime-silicate glasses

International Nuclear Information System (INIS)

Heath, Paul G.; Corkhill, Claire L.; Stennett, Martin C.; Hand, Russell J.; Meyer, Willem C.H.M.; Hyatt, Neil C.

2013-01-01

Tri-Structural Isotropic (TRISO) coated particle-fuel is a key component in designs for future high temperature nuclear reactors. This study investigated the suitability of three soda lime silicate glass compositions, for the encapsulation of simulant TRISO particle fuel. A cold press and sinter (CPS) methodology was employed to produce TRISO particle–glass composites. Composites produced were determined to have an aqueous durability, fracture toughness and Vickers’ hardness comparable to glasses currently employed for the disposal of high level nuclear wastes. Sintering at 700 °C for 30 min was found to remove all interconnected porosity from the composite bodies and oxidation of the outer pyrolytic carbon layer during sintering was prevented by processing under a 5% H 2 /N 2 atmosphere. However, the outer pyrolytic carbon layer was not effectively wetted by the encapsulating glass matrix. The aqueous durability of the TRISO particle–glass composites was investigated using PCT and MCC-1 tests combined with geochemical modelling. It was found that durability was dependent on silicate and calcium solution saturation. This study provides significant advancements in the preparation of TRISO particle encapsulant waste forms. The potential for the use of non-borosilicate sintered glass composites for TRISO particle encapsulation has been confirmed, although further refinements are required

Encapsulation of TRISO particle fuel in durable soda-lime-silicate glasses

Energy Technology Data Exchange (ETDEWEB)

Heath, Paul G.; Corkhill, Claire L.; Stennett, Martin C.; Hand, Russell J. [Immobilisation Science Laboratory, Department of Materials Science and Engineering, Robert Hadfield Building, University of Sheffield, Sheffield S1 3JD (United Kingdom); Meyer, Willem C.H.M. [Necsa, South African Nuclear Energy Corporation, PO Box 582, Pretoria, Gauteng (South Africa); Hyatt, Neil C., E-mail: n.c.hyatt@sheffield.ac.uk [Immobilisation Science Laboratory, Department of Materials Science and Engineering, Robert Hadfield Building, University of Sheffield, Sheffield S1 3JD (United Kingdom)

2013-05-15

Tri-Structural Isotropic (TRISO) coated particle-fuel is a key component in designs for future high temperature nuclear reactors. This study investigated the suitability of three soda lime silicate glass compositions, for the encapsulation of simulant TRISO particle fuel. A cold press and sinter (CPS) methodology was employed to produce TRISO particle–glass composites. Composites produced were determined to have an aqueous durability, fracture toughness and Vickers’ hardness comparable to glasses currently employed for the disposal of high level nuclear wastes. Sintering at 700 °C for 30 min was found to remove all interconnected porosity from the composite bodies and oxidation of the outer pyrolytic carbon layer during sintering was prevented by processing under a 5% H{sub 2}/N{sub 2} atmosphere. However, the outer pyrolytic carbon layer was not effectively wetted by the encapsulating glass matrix. The aqueous durability of the TRISO particle–glass composites was investigated using PCT and MCC-1 tests combined with geochemical modelling. It was found that durability was dependent on silicate and calcium solution saturation. This study provides significant advancements in the preparation of TRISO particle encapsulant waste forms. The potential for the use of non-borosilicate sintered glass composites for TRISO particle encapsulation has been confirmed, although further refinements are required.

Polymer-Layer Silicate Nanocomposites

DEFF Research Database (Denmark)

Potarniche, Catalina-Gabriela

Nowadays, some of the material challenges arise from a performance point of view as well as from recycling and biodegradability. Concerning these aspects, the development of polymer layered silicate nanocomposites can provide possible solutions. This study investigates how to obtain polymer layered...... with a spectacular improvement up to 300 % in impact strength were obtained. In the second part of this study, layered silicate bio-nanomaterials were obtained starting from natural compounds and taking into consideration their biocompatibility properties. These new materials may be used for drug delivery systems...... and as biomaterials due to their high biocompatible properties, and because they have the advantage of being biodegradable. The intercalation process of natural compounds within silicate platelets was investigated. By uniform dispersing of binary nanohybrids in a collagen matrix, nanocomposites with intercalated...

LABORATORY INVESTIGATIONS OF SILICATE MUD CONTAMINATION WITH CALCIUM

Directory of Open Access Journals (Sweden)

Nediljka Gaurina-Međimurec

2004-12-01

Full Text Available The silicate-based drilling fluid is a low solids KCl/polymer system with the addition of soluble sodium or potassium silicate to enhance inhibition and wellbore stability. Silicate-based drilling fluids exhibit remarkable shale and chalk stabilizing properties, resulting in gauge hole and the formation of firm cuttings when drilling reactive shales and soft chalks. Silicates protect shales by in-situ gellation when exposed to the neutral pore fluid and precipitation, which occurs on contact with divalent ions present at the surface of the shale. Also, silicates prevent the dispersion and washouts when drilling soft chalk by reacting with the Ca2+ ions present on chalk surfaces of cutting and wellbore to form a protective film. The silicate-based drilling fluid can be used during drilling hole section through shale interbeded anhydrite formations because of its superior shale stabilizing characteristics. However, drilling through the anhydrite can decrease the silicate concentration and change rheological and filtration fluid properties. So, the critical concentration of calcium ions should be investigated by lab tests. This paper details the mechanism of shale inhibition using silicate-based drilling fluid, and presents results of lab tests conducted to ascertain the effect of Ca2+ ions on silicate level in the fluid and the fluid properties.

Structures and lithofacies of inferred silicic conduits in the Paraná-Etendeka LIP, southernmost Brazil

Science.gov (United States)

Simões, M. S.; Lima, E. F.; Sommer, C. A.; Rossetti, L. M. M.

2018-04-01

Extensive silicic units in the Paraná-Etendeka LIP have been long interpreted as pyroclastic density currents (rheomorphic ignimbrites) derived from the Messum Complex in Namibia. In recent literature, however, they have been characterized as effusive lava flows and domes. In this paper we describe structures and lithofacies related to postulated silicic lava feeder conduits at Mato Perso, São Marcos and Jaquirana-Cambará do Sul areas in southern Brazil. Inferred conduits are at least 15-25 m in width and the lithofacies include variably vesicular monomictic welded and non-welded breccias in the margins to poorly vesicular, banded, spherulitic and microfractured vitrophyres in the central parts. Flat-lying coherent vitrophyres and massive obsidian are considered to be the subaerial equivalents of the conduits. Large-scale, regional tectonic structures in southern Brazil include the NE-SW aligned Porto Alegre Suture, Leão and Açotea faults besides the Antas Lineament, a curved tectonic feature accompanying the bed of Antas river. South of the Antas Lineament smaller-scale, NW-SE lineaments limit the exposure areas of the inferred conduits. NE-SW and subordinate NW-SE structures within this smaller-scale lineaments are represented by the main postulated conduit outcrops and are parallel to the dominant sub-vertical banding in the widespread banded vitrophyre lithofacies. Upper lava flows display flat-lying foliation, pipe-like and spherical vesicles and have better developed microlites. Petrographic characteristics of the silicic vitrophyres indicate that crystal-poor magmas underwent distinct cooling paths for each inferred conduit area. The vitrophyre chemical composition is defined by the evolution of trachydacitic/dacitic vitrophyres with 62-65 wt% SiO2 to rhyodacite and rhyolite with 66-68 wt% SiO2. The more evolved rocks are assigned to the latest intrusive grey vitrophyre outcropping in the center of the conduits. Degassing pathways formed during

21 CFR 582.2122 - Aluminum calcium silicate.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Aluminum calcium silicate. 582.2122 Section 582.2122 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED....2122 Aluminum calcium silicate. (a) Product. Aluminum calcium silicate. (b) Tolerance. 2 percent. (c...

21 CFR 182.2122 - Aluminum calcium silicate.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Aluminum calcium silicate. 182.2122 Section 182.2122 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED....2122 Aluminum calcium silicate. (a) Product. Aluminum calcium silicate. (b) Tolerance. 2 percent. (c...

Volcanism on differentiated asteroids (Invited)

Science.gov (United States)

Wilson, L.

2013-12-01

The Dawn spacecraft's investigation of 4 Vesta, best-preserved of the early-forming differentiated asteroids, prompts a reappraisal of factors controlling igneous activity on such bodies. Analogy with melt transfer in zones of partial melting on Earth implies that silicate melts moved efficiently within asteroid mantles in complex networks of veins and dikes, so that only a few percent of the mantle consisted of melt at any one time. Thus even in cases where large amounts of mantle melting occurred, the melts did not remain in the mantle to form "magma oceans", but instead migrated to shallow depths. The link between magma flow rate and the stresses needed to keep fractures open and allow flow fast enough to avoid excessive cooling implies that only within asteroids with radii more than ~190-250 km would continuous magma flow from mantle to surface be possible. In all smaller asteroids (including Vesta) magma must have accumulated in sills at the base of the lithosphere (the conductively controlled ~10 km thick thermal boundary layer) or in crustal magma reservoirs near its base. Magma would then have erupted intermittently to the surface from these steadily replenished reservoirs. The average rates of eruption to the surface (or shallow intrusion) should balance the magma production rate, but since magma could accumulate and erupt intermittently from these reservoirs, the instantaneous eruption rates could be hundreds to thousands of cubic m/s, comparable to historic basaltic eruption rates on Earth and very much greater than the average mantle melting rate. The absence of asteroid atmospheres makes explosive eruptions likely even if magmas are volatile-poor. On asteroids with radii less than ~100 km, gases and sub-mm pyroclastic melt droplets would have had speeds exceeding the escape speed assuming a few hundred ppm volatiles, and only cm sized or larger clasts would have been retained. On larger bodies almost all pyroclasts will have returned to the surface

Zircon reveals protracted magma storage and recycling beneath Mount St. Helens

Science.gov (United States)

Claiborne, L.L.; Miller, C.F.; Flanagan, D.M.; Clynne, M.A.; Wooden, J.L.

2010-01-01

Current data and models for Mount St. Helens volcano (Washington, United States) suggest relatively rapid transport from magma genesis to eruption, with no evidence for protracted storage or recycling of magmas. However, we show here that complex zircon age populations extending back hundreds of thousands of years from eruption age indicate that magmas regularly stall in the crust, cool and crystallize beneath the volcano, and are then rejuvenated and incorporated by hotter, young magmas on their way to the surface. Estimated dissolution times suggest that entrained zircon generally resided in rejuvenating magmas for no more than about a century. Zircon elemental compositions reflect the increasing influence of mafic input into the system through time, recording growth from hotter, less evolved magmas tens of thousands of years prior to the appearance of mafic magmas at the surface, or changes in whole-rock geochemistry and petrology, and providing a new, time-correlated record of this evolution independent of the eruption history. Zircon data thus reveal the history of the hidden, long-lived intrusive portion of the Mount St. Helens system, where melt and crystals are stored for as long as hundreds of thousands of years and interact with fresh influxes of magmas that traverse the intrusive reservoir before erupting. ?? 2010 Geological Society of America.

Antibacterial Activity of Silicate Bioceramics

Institute of Scientific and Technical Information of China (English)

HU Sheng; NING Congqin; ZHOU Yue; CHEN Lei; LIN Kaili; CHANG Jiang

2011-01-01

Four kinds of pure silicate ceramic particles, CaSiO3, Ca3SiO5, bredigite and akermanite were prepared and their bactericidal effects were systematically investigated. The phase compositions of these silicate ceramics were characterized by XRD. The ionic concentration meas urement revealed that the Calcium (Ca) ion concentration were relatively higher in Ca3SiO5 and bredigite, and much lower in CaSiO3 and akermanite. Accordingly, the pH values of the four silicate ceramics extracts showed a positive correlation with the particle concentrations. Meanwhile, by decreasing the particle size, higher Ca ion concentrations can be achieved, leading to the increase of aqueous pH value as well. In summary, all of the four silicate ceramics tested in our study showed antibacterial effect in a dose-dependent manner. Generally, the order of their antibacterial activity against E.coli from strong to weak is Ca3SiO5, bredigite, CaSiO3 and akermanite.

TMVOC, simulator for multiple volatile organic chemicals

International Nuclear Information System (INIS)

Pruess, Karsten; Battistelli, Alfredo

2003-01-01

TMVOC is a numerical simulator for three-phase non-isothermal flow of water, soil gas, and a multicomponent mixture of volatile organic chemicals (VOCs) in multidimensional heterogeneous porous media. It is an extension of the TOUGH2 general-purpose simulation program developed at the Lawrence Berkeley National Laboratory. TMVOC is designed for applications to contamination problems that involve hydrocarbon fuel or organic solvent spills in saturated and unsaturated zones. It can model contaminant behavior under ''natural'' environmental conditions, as well as for engineered systems, such as soil vapor extraction, groundwater pumping, or steam-assisted source remediation. TMVOC is upwards compatible with T2VOC (Falta et al., 1995) and can be initialized from T2VOC-style initial conditions. The main enhancements in TMVOC relative to T2VOC are as follows: a multicomponent mixture of volatile organic chemicals can be modeled; any and all combinations of the three phases water-oil-gas are treated; several non-condensible gases may be present; diffusion is treated in all phases in a manner that is fully coupled with phase partitioning. This paper gives a brief summary of the methodology used in TMVOC as well as highlighting some implementation issues. Simulation of a NAPL spill and subsequent remediation is discussed for a 2-D vertical section of a saturated-unsaturated flow problem

Bursting the bubble of melt inclusions

Science.gov (United States)

Lowenstern, Jacob B.

2015-01-01

Most silicate melt inclusions (MI) contain bubbles, whose significance has been alternately calculated, pondered, and ignored, but rarely if ever directly explored. Moore et al. (2015) analyze the bubbles, as well as their host glasses, and conclude that they often hold the preponderance of CO2 in the MI. Their findings entreat future researchers to account for the presence of bubbles in MI when calculating volatile budgets, saturation pressures, and eruptive flux.

Amended Silicated for Mercury Control

Energy Technology Data Exchange (ETDEWEB)

James Butz; Thomas Broderick; Craig Turchi

2006-12-31

Amended Silicates{trademark}, a powdered, noncarbon mercury-control sorbent, was tested at Duke Energy's Miami Fort Station, Unit 6 during the first quarter of 2006. Unit 6 is a 175-MW boiler with a cold-side electrostatic precipitator (ESP). The plant burns run-of-the-river eastern bituminous coal with typical ash contents ranging from 8-15% and sulfur contents from 1.6-2.6% on an as-received basis. The performance of the Amended Silicates sorbent was compared with that for powdered activated carbon (PAC). The trial began with a period of baseline monitoring during which no sorbent was injected. Sampling during this and subsequent periods indicated mercury capture by the native fly ash was less than 10%. After the baseline period, Amended Silicates sorbent was injected at several different ratios, followed by a 30-day trial at a fixed injection ratio of 5-6 lb/MMACF. After this period, PAC was injected to provide a comparison. Approximately 40% mercury control was achieved for both the Amended Silicates sorbent and PAC at injection ratios of 5-6 lbs/MMACF. Higher injection ratios did not achieve significantly increased removal. Similar removal efficiencies have been reported for PAC injection trials at other plants with cold-side ESPs, most notably for plants using medium to high sulfur coal. Sorbent injection did not detrimentally impact plant operations and testing confirmed that the use of Amended Silicates sorbent does not degrade fly ash quality (unlike PAC). The cost for mercury control using either PAC or Amended Silicates sorbent was estimated to be equivalent if fly ash sales are not a consideration. However, if the plant did sell fly ash, the effective cost for mercury control could more than double if those sales were no longer possible, due to lost by-product sales and additional cost for waste disposal. Accordingly, the use of Amended Silicates sorbent could reduce the overall cost of mercury control by 50% or more versus PAC for locations where

Interstellar silicate analogs for grain-surface reaction experiments: Gas-phase condensation and characterization of the silicate dust grains

Energy Technology Data Exchange (ETDEWEB)

Sabri, T.; Jäger, C. [Laboratory Astrophysics Group of the Max Planck Institute for Astronomy at the Friedrich Schiller University Jena Institute of Solid State Physics, Helmholtzweg 3, D-07743 Jena (Germany); Gavilan, L.; Lemaire, J. L.; Vidali, G. [Observatoire de Paris/Université de Cergy-Pontoise, 5 mail Gay Lussac, F-95000 Cergy-Pontoise (France); Mutschke, H. [Laboratory Astrophysics Group of the Astrophysical Institute and University Observatory, Friedrich Schiller University Jena Schillergässchen 3, D-07743 Jena (Germany); Henning, T., E-mail: tolou.sabri@uni-jena.de [Max Planck Institute for Astronomy Königstuhl 17, D-69117 Heidelberg (Germany)

2014-01-10

Amorphous, astrophysically relevant silicates were prepared by laser ablation of siliceous targets and subsequent quenching of the evaporated atoms and clusters in a helium/oxygen gas atmosphere. The described gas-phase condensation method can be used to synthesize homogeneous and astrophysically relevant silicates with different compositions ranging from nonstoichiometric magnesium iron silicates to pyroxene- and olivine-type stoichiometry. Analytical tools have been used to characterize the morphology, composition, and spectral properties of the condensates. The nanometer-sized silicate condensates represent a new family of cosmic dust analogs that can generally be used for laboratory studies of cosmic processes related to condensation, processing, and destruction of cosmic dust in different astrophysical environments. The well-characterized silicates comprising amorphous Mg{sub 2}SiO{sub 4} and Fe{sub 2}SiO{sub 4}, as well as the corresponding crystalline silicates forsterite and fayalite, produced by thermal annealing of the amorphous condensates, have been used as real grain surfaces for H{sub 2} formation experiments. A specifically developed ultra-high vacuum apparatus has been used for the investigation of molecule formation experiments. The results of these molecular formation experiments on differently structured Mg{sub 2}SiO{sub 4} and Fe{sub 2}SiO{sub 4} described in this paper will be the topic of the next paper of this series.

Stratigraphy, distribution, and evidence for mafic triggering of the ca. 8.5 ka Driftwood Pumice eruption, Makushin Volcano, Alaska, U.S.A

Science.gov (United States)

Lerner, Allan H.; Crowley, Peter D.; Nicolaysen, Kirsten P.; Hazlett, Richard W.

2018-05-01

Makushin Volcano on Unalaska Island, Alaska, threatens the Aleutian's largest population centers (Unalaska and Dutch Harbor), yet its eruption mechanisms are poorly known. This study presents a detailed stratigraphic and geochemical investigation of Makushin's most recent highly explosive event: the ca. 8.5 ka Driftwood Pumice eruption. The Driftwood Pumice has measured thicknesses of over 2.5 m, and isopach reconstructions estimate a total deposit volume of 0.3 to 1.6 km3, indicating a VEI 4-5 eruption. Proximal deposits consist of normally-graded, tan, dacitic to andesitic pumice, capped by a thinner dark layer of lower-silica andesitic scoria mixed with abundant lithic fragments. This stratigraphy is interpreted as an initial vent-clearing eruption that strengthened into a climactic ejection of pumice and ash and concluded with vent destabilization and the eruption of somewhat more mafic, gas-poor magma. Within the pumice, geochemical trends, disequilibrium mineral populations, and mineral zonation patterns show evidence of magma mixing between a bulk silicic magma and a mafic melt. Euhedral high-Ca plagioclase (An68-91) and high-Mg olivine (Fo69-77) phenocrysts are in disequilibrium with trachydacitic glass (65-68 wt% SiO2) and more abundant sodic plagioclase (An34-55), indicating the former originally crystallized in a more mafic melt. Tephra whole rock compositions become more mafic upwards through the deposit, ranging from a basal low-silica dacite to an andesite (total range: 60.8-63.3 wt% SiO2). Collectively, these compositional variations suggest magma mixing in the Driftwood Pumice (DWP) magma reservoir, with a systematic increase in the amount of a mafic component (up to 25%) upward through the deposit. Olivine-liquid and liquid-only thermometry indicate the mafic magma intruded at temperatures 140-200 °C hotter than the silicic magma. Diffusion rates calculated for 5-7 μm thick, lower-Mg rims on the olivine phenocrysts (Fo60 rim vs Fo76 bulk) suggest

A petrogenetic model of the relationships among achondritic meteorites

Science.gov (United States)

Stolper, E.; Hays, J. F.; Mcsween, H. Y., Jr.

1979-01-01

Petrological evidence is used to support the hypothesis that although the magma source regions and parent bodies of basaltic achondrite, shergottite, nakhlite, and chassignite meteorites are clearly distinct, they may be simply related. It is proposed that the peridotites which on partial melting generated the parent magmas of the shergottite meteorites differed from those which gave rise to eucritic magmas by being enriched in a component rich in alkalis and other volatiles. Similarly, the source regions of the parent magmas of the nakhlite and chassignite meteorites differed from those on the shergottite parent body by being still richer in this volatile-rich component. These regions could have been related by processes such as mixture of variable amounts of volatile-rich and volatile-poor components in planetary or nebular settings, or alternatively by variable varying degrees of volatile loss from volatile-rich materials.

Shallow magma diversions during explosive diatreme-forming eruptions.

Science.gov (United States)

Le Corvec, Nicolas; Muirhead, James D; White, James D L

2018-04-13

The diversion of magma is an important mechanism that may lead to the relocation of a volcanic vent. Magma diversion is known to occur during explosive volcanic eruptions generating subterranean excavation and remobilization of country and volcanic rocks. However, feedbacks between explosive crater formation and intrusion processes have not been considered previously, despite their importance for understanding evolving hazards during volcanic eruptions. Here, we apply numerical modeling to test the impacts of excavation and subsequent infilling of diatreme structures on stress states and intrusion geometries during the formation of maar-diatreme complexes. Explosive excavation and infilling of diatremes affects local stress states which inhibits magma ascent and drives lateral diversion at various depths, which are expected to promote intra-diatreme explosions, host rock mixing, and vent migration. Our models demonstrate novel mechanisms explaining the generation of saucer-shaped sills, linked with magma diversion and enhanced intra-diatreme explosive fragmentation during maar-diatreme volcanism. Similar mechanisms will occur at other volcanic vents producing crater-forming eruptions.

Io: Loki Patera as a Magma Sea

Science.gov (United States)

Matson, Dennis L.; Davies, Ashley Gerard; Veeder, Glenn J.; Rathbun, Julie A.; Johnson, Torrence V.; Castillo, Julie C.

2006-01-01

We develop a physical model for Loki Patera as a magma sea. We calculate the total volume of magma moving through the Loki Patera volcanic system every resurfacing cycle (approx.540 days) and the resulting variation in thermal emission. The rate of magma solidification at times reaches 3 x 10(exp 6) kg per second, with a total solidified volume averaging 100 cu km per year. A simulation of gas physical chemistry evolution yields the crust porosity profile and the timescale when it will become dense enough to founder in a manner consistent with observations. The Loki Patera surface temperature distribution shows that different areas are at different life cycle stages. On a regional scale, however, there can be coordinated activity, indicated by the wave of thermal change which progresses from Loki Patera's SW quadrant toward the NE at a rate of approx.1 km per day. Using the observed surface temperature distribution, we test several mechanisms for resurfacing Loki Patera, finding that resurfacing with lava flows is not realistic. Only the crustal foundering process is consistent with observations. These tests also discovered that sinking crust has a 'heat deficit' which promotes the solidification of additional magma onto the sinking plate ("bulking up"). In the limiting case, the mass of sinking material can increase to a mass of approx.3 times that of the foundering plate. With all this solid matter sinking, there is a compensating upward motion in the liquid magma. This can be in excess of 2 m per year. In this manner, solid-liquid convection is occurring in the sea.

Effect of moisture and chitosan layered silicate on morphology and properties of chitosan/layered silicates films

International Nuclear Information System (INIS)

Silva, J.R.M.B. da; Santos, B.F.F. dos; Leite, I.F.

2014-01-01

Thin chitosan films have been for some time an object of practical assessments. However, to obtain biopolymers capable of competing with common polymers a significant improvement in their properties is required. Currently, the technology of obtaining polymer/layered silicates nanocomposites has proven to be a good alternative. This work aims to evaluate the effect of chitosan content (CS) and layered silicates (AN) on the morphology and properties of chitosan/ layered silicate films. CS/AN bionanocomposites were prepared by the intercalation by solution in the proportion 1:1 and 5:1. Then were characterized by infrared spectroscopy (FTIR), diffraction (XRD) and X-ray thermogravimetry (TG). It is expected from the acquisition of films, based on different levels of chitosan and layered silicates, choose the best composition to serve as a matrix for packaging drugs and thus be used for future research. (author)

VOLATILECALC: A silicate melt-H2O-CO2 solution model written in Visual Basic for excel

Science.gov (United States)

Newman, S.; Lowenstern, J. B.

2002-01-01

We present solution models for the rhyolite-H2O-CO2 and basalt-H2O-CO2 systems at magmatic temperatures and pressures below ~ 5000 bar. The models are coded as macros written in Visual Basic for Applications, for use within MicrosoftR Excel (Office'98 and 2000). The series of macros, entitled VOLATILECALC, can calculate the following: (1) Saturation pressures for silicate melt of known dissolved H2O and CO2 concentrations and the corresponding equilibrium vapor composition; (2) open- and closed-system degassing paths (melt and vapor composition) for depressurizing rhyolitic and basaltic melts; (3) isobaric solubility curves for rhyolitic and basaltic melts; (4) isoplethic solubility curves (constant vapor composition) for rhyolitic and basaltic melts; (5) polybaric solubility curves for the two end members and (6) end member fugacities of H2O and CO2 vapors at magmatic temperatures. The basalt-H2O-CO2 macros in VOLATILECALC are capable of calculating melt-vapor solubility over a range of silicate-melt compositions by using the relationships provided by Dixon (American Mineralogist 82 (1997) 368). The output agrees well with the published solution models and experimental data for silicate melt-vapor systems for pressures below 5000 bar. ?? 2002 Elsevier Science Ltd. All rights reserved.

Silicate melt metasomatism in the lithospheric mantle beneath SW Poland

Science.gov (United States)

Puziewicz, Jacek; Matusiak-Małek, Magdalena; Ntaflos, Theodoros; Grégoire, Michel; Kukuła, Anna

2014-05-01

The xenoliths of peridotites representing the subcontinental lithospheric mantle (SCLM) beneath SW Poland and adjacent parts of Germany occur in the Cenozoic alkaline volcanic rocks. Our study is based on detailed characterization of xenoliths occurring in 7 locations (Steinberg in Upper Lusatia, Księginki, Pilchowice, Krzeniów, Wilcza Góra, Winna Góra and Lutynia in Lower Silesia). One of the two major lithologies occurring in the xenoliths, which we call the "B" lithology, comprises peridotites (typically harzburgites) with olivine containing from 90.5 to 84.0 mole % of forsterite. The harzburgites contain no clinopyroxene or are poor in that mineral (eg. in Krzeniów the group "B" harzburgites contain pfu in ortho-, and pfu in clinopyroxene). The exception are xenoliths from Księginki, which contain pyroxenes characterised by negative correlation between mg# and Al. The REE patterns of both ortho- and clinopyroxene in the group "B" peridotites suggest equilibration with silicate melt. The rocks of "B" lithology were formed due to alkaline silicate melt percolation in the depleted peridotitic protolith. The basaltic melts formed at high pressure are usually undersaturated in both ortho- and clinopyroxene at lower pressures (Kelemen et al. 1992). Because of cooling and dissolution of ortho- and clinopyroxene the melts change their composition and become saturated in one or both of those phases. Experimental results (e.g. Tursack & Liang 2012 and references therein) show that the same refers to alkaline basaltic silicate melts and that its reactive percolation in the peridotitic host leads to decrease of Mg/(Mg+Fe) ratios of olivine and pyroxenes. Thus, the variation of relative volumes of olivine and orthopyroxene as well as the decrease of mg# of rock-forming silicates is well explained by reactive melt percolation in the peridotitic protolith consisting of high mg# olivine and pyroxenes (in the area studied by us that protolith was characterised by olivine

Sulfur release from the Columbia River Basalts and other flood lava eruptions constrained by a model of sulfide saturation

Science.gov (United States)

Blake, S.; Self, S.; Sharma, K.; Sephton, S.

2010-11-01

A very likely cause of widespread environmental impacts of flood basalt eruptions is the emission of sulfur, chlorine, and possibly fluorine from the erupting magma. We present new data on the S contents of rare glass inclusions and matrix glasses preserved in quenched lava selvages from lava fields of the Columbia River Basalt Group (CRBG; Ginkgo, Sand Hollow and Sentinel Gap flows, Wanapum Basalt Formation). We compare these results with published data from Neral and Jawar Formation lavas (Deccan Traps, India) and the Roza flow (CRBG). CRBG glass inclusions have up to 2000 ppm S and 15-16 wt.% FeO total. By contrast, the Deccan examples have about 1400 ppm S and 10 wt.% FeO total. Several of the glass inclusions are partly degassed, indicating entrapment during magma rise, and matrix glasses are typically more evolved than glass inclusions due to small amounts of in situ crystallization. Using only the highest S inclusions and taking account of the effect of in situ crystallization and degassing on the S content of the residual matrix glasses indicates S yields of about 0.07 to 0.1 wt.% from Deccan eruptions and about 0.15 wt.% from Wanapum (CRBG) eruptions. The pre-eruptive S contents of these magmas correlate with weight% FeO total in the same way as undegassed sulfide-saturated mid-ocean ridge basalts. Using oceanic basalts to define a sulfide saturation line, and data on S contents of degassed basalts, we propose an equation to estimate the weight% S yield (ΔS) from initially sulfide-saturated basalt liquid without the need to find well-preserved, rare, undegassed glass inclusions and matrix glasses: ΔS=(0.01418×FeO-0.06381)±0.02635. This compares well with independent estimates derived from the petrologic method by taking the difference in S concentration of glass inclusions and matrix glass. Applying our method to the aphyric Grande Ronde Basalts of the CRBG implies a total yield of about 1000 Gt SO 2 delivered into the Miocene atmosphere in

Decompression Induced Crystallization of Basaltic Andesite Magma: Constraints on the Eruption of Arenal Volcano, Costa Rica.

Science.gov (United States)

Szramek, L. A.; Gardner, J. E.; Larsen, J. F.

2004-12-01

Arenal Volcano is a small stratovolcano located 90 km NW of San Jose, Costa Rica. In 1968 current activity began with a Plinian phase, and has continued to erupt lava flows and pyroclastic flows intermittently since. Samples from the Plinian, pyroclastic flow, strombolian, and effusive phases have been studied texturally. Little variation in crystallinity occurs amongst the different phases. Number density of crystals, both 2D and 3D are 50-70 mm-2 and 30,000-50,000 mm-3 in the Plinian sample, compared to the lesser values in other eruptive types. Characteristic crystal size also increases as explosivity decreases. Two samples, both lava flows collected while warm, overlap with the Plinian sample. This suggests that the variations seen may be a result of cooling history. Plagioclase differs between the Plinian sample, in which they are only tabular in shape, and the other eruptive types, which contain both tabular and equant crystals. To link decompression paths of the Arenal magma to possible pre-eruptive conditions, we have carried out hydrothermal experiments. The experiments were preformed in TZM pressure vessels buffered at a fugacity of Ni-NiO and water saturation. Phase equilibria results in conjunction with mineral compositions and temperature estimates by previous workers from active lava flows and two-pyroxene geothermometry, constrain the likely pre-eruptive conditions for the Arenal magma to 950-1040° C with a water pressure of 50-80 MPa. Samples that started from conditions that bracket our estimated pre-eruptive conditions were decompressed in steps of 5-30 MPa and held for various times at each step until 20 MPa was reached, approximating average decompression rates of 0.25, 0.025, 0.0013 MPa/s. Comparison of textures found in the natural samples to the experimentally produced textures suggest that the Plinian eruption likely was fed by magma ascending at 0.05-1 m/s, whereas the less explosive phases were fed by magma ascending at 0.05 m/s or less.

Toward an integrative spatiotemporal architecture of the magma plumbing system leading to systematic Plinian eruption at Montagne Pelée Martinique (Lesser Antilles)

Science.gov (United States)

Boudon, G.; Balcone-Boissard, H.; Lyonnet, E.; Morgan, D. J.

2017-12-01

The dynamic of crustal magma reservoir may be at the origin of pressure/temperature variations that may trigger magma ascent and eruption. These changes can be registered during crystal growth and can probably produce at the surface geophysical or/and geochemical signals that could be registered by monitoring network, constituting precursory signals. For volcanoes where the plumbing system is well established in terms of volume and depth for a given cycle, repetitive eruptions of the same order of magnitude and involving similar magma composition may occur. It was the case for Montagne Pelée (Martinique, Lesser Antilles), sadly known for the 1902 lava dome-forming eruption that killed 30 000 inhabitants, and that produce repetitive Plinian eruptions in the last 15 ky. Are the perturbations in the dynamic of the magma storage identical for all these eruptions and is the timescale between these perturbations and the eruptions in the same order of magnitude? In the last decade, intracristalline diffusion modelling has been increasingly used to constrain timescale of magmatic processes. Recently this kind of investigations has been coupled to a petrological model of the magma storage region to better wholly describe its behaviour through a Crystal System Analysis (CSA) approach. Here we aim at constraining the pre-eruptive dynamic of the reservoir giving birth to the Plinian eruptions at Montagne Pelée. Precisely we attempt to identify the processes at the origin of the eruptions and the timescale between this process and the eruption. By studying the last five Plinian eruptions of this volcano the question of the systematic occurrence of one process at the same time prior eruption will be discussed. To achieve this goal we performed a detailed petrological description of the eruptive products of the first Plinian phase of these eruptions to build a CSA tree through EPMA and SEM analyses, coupled to Fe-Mg diffusion modelling in orthopyroxenes to retrieve timescale

Stochastic volatility of volatility in continuous time

DEFF Research Database (Denmark)

Barndorff-Nielsen, Ole; Veraart, Almut

This paper introduces the concept of stochastic volatility of volatility in continuous time and, hence, extends standard stochastic volatility (SV) models to allow for an additional source of randomness associated with greater variability in the data. We discuss how stochastic volatility...... of volatility can be defined both non-parametrically, where we link it to the quadratic variation of the stochastic variance process, and parametrically, where we propose two new SV models which allow for stochastic volatility of volatility. In addition, we show that volatility of volatility can be estimated...

Coupled interactions between volatile activity and Fe oxidation state during arc crustal processes

Science.gov (United States)

Humphreys, Madeleine C.S.; Brooker, R; Fraser, D.C.; Burgisser, A; Mangan, Margaret T.; McCammon, C

2015-01-01

Arc magmas erupted at the Earth’s surface are commonly more oxidized than those produced at mid-ocean ridges. Possible explanations for this high oxidation state are that the transfer of fluids during the subduction process results in direct oxidation of the sub-arc mantle wedge, or that oxidation is caused by the effect of later crustal processes, including protracted fractionation and degassing of volatile-rich magmas. This study sets out to investigate the effect of disequilibrium crustal processes that may involve coupled changes in H2O content and Fe oxidation state, by examining the degassing and hydration of sulphur-free rhyolites. We show that experimentally hydrated melts record strong increases in Fe3+/∑Fe with increasing H2O concentration as a result of changes in water activity. This is relevant for the passage of H2O-undersaturated melts from the deep crust towards shallow crustal storage regions, and raises the possibility that vertical variations in fO2 might develop within arc crust. Conversely, degassing experiments produce an increase in Fe3+/∑Fe with decreasing H2O concentration. In this case the oxidation is explained by loss of H2 as well as H2O into bubbles during decompression, consistent with thermodynamic modelling, and is relevant for magmas undergoing shallow degassing en route to the surface. We discuss these results in the context of the possible controls on fO2 during the generation, storage and ascent of magmas in arc settings, in particular considering the timescales of equilibration relative to observation as this affects the quality of the petrological record of magmatic fO2.

The expected greenhouse benefits from developing magma power at Long Valley, California

International Nuclear Information System (INIS)

Haraden, John.

1995-01-01

Magma power is the production of electricity from shallow magma bodies. Before magma becomes a practical source of power, many engineering problems must still be solved. When they are solved, the most likely site for the first magma power plant is Long Valley, California, USA. In this paper, we examine the greenhouse benefits from developing Long Valley. By generating magma power and by curtailing an equal amount of fossil power, we estimate the expected mass and the expected discounted value of reduced CO 2 emissions. For both measures, the expected benefits seem to be substantial. (author)

Magma chamber processes in central volcanic systems of Iceland

DEFF Research Database (Denmark)

Þórarinsson, Sigurjón Böðvar; Tegner, Christian

2009-01-01

are composed of 2-10 m thick melanocratic layers rich in clinopyroxene and sometimes olivine, relative to the thicker overlying leucocratic oxide gabbros. While the overall compositional variation is limited (Mg# clinopyroxene 72-84; An% plagioclase 56-85), the melanocratic bases display spikes in Mg# and Cr2O......3 of clinopyroxene and magnetite indicative of magma replenishment. Some macrorhythmic units show mineral trends indicative of up-section fractional crystallisation over up to 100 m, whereas others show little variation. Two populations of plagioclase crystals (large, An-rich and small, less An......-rich) indicate that the recharge magma carried plagioclase xenocrysts (high An-type). The lack of evolved gabbros suggests formation in a dynamic magma chamber with frequent recharge, tapping and fractionation. Modelling of these compositional trends shows that the parent magma was similar to known transitional...

The 1994-2001 eruptive period at Rabaul, Papua New Guinea: Petrological and geochemical evidence for basalt injections into a shallow dacite magma reservoir, and significant SO2 flux

Science.gov (United States)

Patia, H.; Eggins, S. M.; Arculus, R. J.; McKee, C. O.; Johnson, R. W.; Bradney, A.

2017-10-01

The eruptions that began at Rabaul Caldera on 19 September 1994 had two focal points, the vents Tavurvur and Vulcan, located 6 km apart on opposing sides of the caldera. Vulcan eruptives define a tight cluster of dacite compositions, whereas Tavurvur eruptives span an array from equivalent dacite compositions to mafic andesites. The eruption of geochemically and mineralogically identical dacites from both vents indicates sourcing from the same magma reservoir. This, together with previously reported H2O-CO2 volatile contents of dacite melt inclusions, a caldera-wide seismic low-velocity zone, and a seismically active caldera ring fault structure are consistent with the presence at 3-6 km depth of an extensive, tabular dacitic magma body having volume of about 15-150 km3. The Tavurvur andesites form a linear compositional array and have strongly bimodal phenocryst assemblages that reflect dacite hybridisation with a mafic basalt. The moderately large volume SO2 flux documented in the Tavurvur volcanic plume (and negligible SO2 flux in the Vulcan plume) combined with high dissolved S contents of basaltic melt inclusions trapped in olivine of Tavurvur eruptives, indicate that the amount of degassed basaltic magma was 0.1 km3 and suggest that the injection of this magma was confined to the Tavurvur-side (eastern to northeastern sector) of the caldera. Circumstantial evidence suggests that the eruption was triggered and evolved in response to a series of basaltic magma injections that may have commenced in 1971 and continued up until at least the start of the 1994 eruptions. The presence of zoned plagioclase phenocrysts reflecting older basalt-dacite interaction events (i.e. anorthite cores overgrown with thick andesine rims), evaluation of limited available data for the products of previous eruptions in 1878 and 1937-1943, and the episodic occurrence of major intra-caldera seismo-deformational events indicates that the shallow magma system at Rabaul Caldera is

Method of chemical analysis of silicate rocks (1962); Methode d'analyse chimique des roches silicatees (1962)

Energy Technology Data Exchange (ETDEWEB)

Pouget, R [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1962-07-01

A rapid method of analysis for the physical and chemical determination of the major constituents of silicate rocks is described. Water losses at 100 deg. C and losses of volatile elements at 1000 deg. C are estimated after staying in oven for these temperatures, or by mean of a thermo-balance. The determination of silica is made by a double insolubilization with hydrochloric acid on attack solution with sodium carbonate; total iron and aluminium, both with calcium and magnesium, after ammoniacal precipitation of Fe and Al, are determined on the filtration product of silica by titrimetry-photometry of their complexes with EDTA. The alkalis Na and K by flame spectrophotometry, Mn by colorimetry of the permanganate, and Ti by mean of his complex with H{sub 2}O{sub 2}, are determined on fluosulfuric attack solution. Phosphorus is determined by his complex with 'molybdenum blue' on a fluoro-nitro-boric attack solution; iron is estimated by potentiometry, with the help of bichromate on hydrofluoric solution. (author) [French] Une methode d'analyse rapide est decrite pour la determination physico-chimique des constituants principaux des roches silicatees. Les pertes en eau a 100 deg. C et en matieres volatiles a 1000 deg. C sont evaluees apres passage au four a ces temperatures, ou a l'aide d'une thermobalance. La determination de la silice se fait par double insolubilisation a l'acide chlorhydrique, sur une attaque au carbonate de sodium; le fer total et l'aluminium ainsi que le calcium et le magnesium, apres precipitation a l'ammoniaque des deux premiers metaux, sont determines sur le filtrat de la silice par titrimetrie-photometrie de leurs complexes avec l'E.D.T.A. Les alcalins sodium et potassium par spectrophotometrie de flamme, le manganese par colorimetrie du permanganate, le titane a l'aide de son complexe avec l'eau oxygenee, sont determines sur une attaque fluosulfurique. Le phosphore est determine par son complexe du 'bleu de molybdene' sur une attaque fluo

Adsorption of aqueous silicate on hematite

International Nuclear Information System (INIS)

Taylor, P.; Ticknor, K.V.

1997-08-01

During radioisotope sorption studies, adsorption of silicate from synthetic groundwaters by synthetic hematite was observed. To further investigate this observation, the adsorption of silicate onto hematite (α-Fe 2 O 3 ) powder from a neutral, aqueous NaC1 solution (0.1 mol/dm 3 ), containing 2.56 x 10 -4 mol/dm 3 of Si added as Na 2 SiO 3 ·9H 2 O, was measured at ∼21 deg C. Equilibrium adsorption of silicate amounted to ∼1.93 μmol/m 2 (one Si(O,OH) 4 moiety per 86 A 2 ). It is important to take this adsorption into account when evaluating the ability of iron oxides to adsorb other species, especially anions, from groundwaters. Silicate adsorption is known to diminish the ability of iron oxides to adsorb other anions. (author)

Temporal evolution of granitic magmas in the Luanchuan metallogenic belt, east Qinling Orogen, central China: Implications for Mo metallogenesis

Science.gov (United States)

Li, Dong; Han, Jiangwei; Zhang, Shouting; Yan, Changhai; Cao, Huawen; Song, Yaowu

2015-11-01

The Luanchuan metallogenic belt, located within the eastern part of the Qinling Orogen, central China, hosts a number of world-class Mo deposits that are closely related to small late Mesozoic granitic plutons. Zircon U-Pb dating of distinct plutons in the Luanchuan metallogenic belt has yielded ages of 153 ± 1, 154 ± 2, 152 ± 2, and 148 ± 1 Ma. Molybdenite Re-Os isotopic compositions of Yuku ore district in the southern part of Luanchuan metallogenic belt has yielded an isochron age of 146 ± 1 Ma, which is consistent with the large-scale mineralization ages in the northern part of the Luanchuan metallogenic belt. A combination of previous studies and new geochronological and isotopic data show a concordant temporal and genetic link between granitic magmatism and Mo mineralization in the Luanchuan metallogenic belt, suggesting that this mineralization episode formed the most extensive Mo mineralization belt in the east Qinling Orogen. Zircon grains from Mo-related granitic plutons show similar trace element distributions. High-precision Multi Collector-Inductively Coupled Plasma-Mass Spectrometry (MC-ICP-MS) Pb isotope analysis of K-feldspar megacrysts from mineralization-related granites suggest that they were derived from the lower crust. Similarly, the Pb isotopic compositions of pyrite coprecipitated with molybdenite also suggest that the metals were derived form the lower crust, with probably minor mantle contribution. A continuum mineralization model that describes the sourcing of Mo from an evolving granitic magma over successive differentiation events, possibly in separate but connected magma chambers, could explain the remarkable Mo enrichment in the Luanchuan metallogenic belt. The volatile- and Mo-bearing granitic magmas ascended as diapirs from the deep crust, and were emplaced as dikes in the upper crust. Lithological differences between these Mo-bearing granites may relate to different stages in the evolution of individual magmas. Finally, ore

The role of amphibole in Merapi arc magma petrogenesis: insights from petrology and geochemistry of lava hosted xenoliths and xenocrysts

Science.gov (United States)

Chadwick, J. P.; Troll, V. R.; Schulz, B.; Dallai, L.; Freda, C.; Schwarzkopf, L. M.; Annersten, H.; Skogby, H.

2010-05-01

deep- to mid-crustal processes given the stability field of amphibole. The individual amphibole xenocrysts are also co-genetic to the Merapi magma system and indicative of high-pressure crystallisation. Hydrogen isotope analyses of these large amphibole megacrysts, record a broad range of dD ratios (permil deviation of D/H isotope ratio from Standard Mean Ocean Water). The dD values of some of these crystals appear to be modified significantly from expected primary compositions, particularly towards the rims of amphiboles showing breakdown textures. The measured dD values possibly result from H-isotope re-equilibration with surrounding volatile vapour during eruption or via dehydration reactions. Mossbauer analysis of a selected pristine amphibole megacryst from this suite records 67 % of iron as Fe3+ in the M-sites. Complementary IR spectroscopy of this amphibole indicates no serious loss of OH groups. High H2O pressures at formation depth for this crystal have stabilized full hydrous compositions at ~ 2% H2O concentration in the amphibole. Such fully hydrated amphiboles could release their H2O on depressurisation on ascent prior to eruption, a process that consistent with the dD data. Analysis of these samples is ongoing, however this initial data indicates that amphibole is a key phase in Merapi magmatic evolution and is a likely source of volatiles through dehydration on ascent. This is of particular significance given the fact that water content of magma has a considerable impact on the explosive potential of subduction zone volcanism. (1) Davidson et al., 2007. Geology, 35: 787-790. (2) Tiepolo et al., 2002 Contrib. Min. Pet., 144:1-15.

Silicates materials of high vacuum technology

CERN Document Server

Espe, Werner

2013-01-01

Materials of High Vacuum Technology, Volume 2: Silicates covers silicate insulators of special importance to vacuum technology. The book discusses the manufacture, composition, and physical and chemical properties of technical glasses, quartz glass, quartzware, vycor glass, ceramic materials, mica, and asbestos.

Petrogenesis of pelitic xenoliths at the Babbitt CuNi deposit, Duluth Complex, Minnesota, U.S.A.

Science.gov (United States)

Ripley, Edward M.; Alawi, Jomaah A.

1988-02-01

The Babbitt deposit consists of disseminated CuFeNi sulfides found within mafic rocks of the Duluth Complex, generally near contacts with underlying metasedimentary rock types. Host rocks for the deposit include troctolites, olivine gabbros, gabbronorites, norites, and occasionally country rock hornfels. Xenoliths of country rocks are abundant in the deposit, and suggest a relationship between sulfide mineralization and country rock contamination. Country rocks in the Babbitt area include those of the middle Precambrian Biwabik Iron Formation, and both calcareous and non-calcareous pelites of the Virginia Formation. Xenoliths contain the assemblage cordierite-plagioclase-biotite-orthopyroxene, and are thought to have been derived from Virginia Formation protoliths. Comparison of protoliths and xenoliths using composition-volume, element ratio and mass-balance techniques suggests that xenoliths have been strongly depleted in volatiles, alkalis and Si. Footwall rocks show only a depletion in volatiles. Neither fluid-phase transport nor diffusion through an intergranular fluid can account for the mass of material transferred. Extensive partial melting of xenoliths, with residual enrichment of FeO, MgO and Al 2O 3, is the most viable transfer process. The lack of SiO 2 concentration gradients around xenoliths and anomalous igneous rock compositions suggest that desilicification occurred at a time when physical mixing of extracted partial melt and host magma was possible, and prior to final emplacement. Sulfide saturation may have been initiated due to Si assimilation with an auxiliary magma chamber. However, the composition of ores in the Babbitt deposit is consistent with saturation being achieved by addition of sediment-derived volatile sulfur, independent of major-element assimilation.

Extensive, water-rich magma reservoir beneath southern Montserrat

Science.gov (United States)

Edmonds, M.; Kohn, S. C.; Hauri, E. H.; Humphreys, M. C. S.; Cassidy, M.

2016-05-01

South Soufrière Hills and Soufrière Hills volcanoes are 2 km apart at the southern end of the island of Montserrat, West Indies. Their magmas are distinct geochemically, despite these volcanoes having been active contemporaneously at 131-129 ka. We use the water content of pyroxenes and melt inclusion data to reconstruct the bulk water contents of magmas and their depth of storage prior to eruption. Pyroxenes contain up to 281 ppm H2O, with significant variability between crystals and from core to rim in individual crystals. The Al content of the enstatites from Soufrière Hills Volcano (SHV) is used to constrain melt-pyroxene partitioning for H2O. The SHV enstatite cores record melt water contents of 6-9 wt%. Pyroxene and melt inclusion water concentration pairs from South Soufriere Hills basalts independently constrain pyroxene-melt partitioning of water and produces a comparable range in melt water concentrations. Melt inclusions recorded in plagioclase and in pyroxene contain up to 6.3 wt% H2O. When combined with realistic melt CO2 contents, the depth of magma storage for both volcanoes ranges from 5 to 16 km. The data are consistent with a vertically protracted crystal mush in the upper crust beneath the southern part of Montserrat which contains heterogeneous bodies of eruptible magma. The high water contents of the magmas suggest that they contain a high proportion of exsolved fluids, which has implications for the rheology of the mush and timescales for mush reorganisation prior to eruption. A depletion in water in the outer 50-100 μm of a subset of pyroxenes from pumices from a Vulcanian explosion at Soufrière Hills in 2003 is consistent with diffusive loss of hydrogen during magma ascent over 5-13 h. These timescales are similar to the mean time periods between explosions in 1997 and in 2003, raising the possibility that the driving force for this repetitive explosive behaviour lies not in the shallow system, but in the deeper parts of a vertically

Magma mixing in granitic rocks of the central Sierra Nevada, California

Science.gov (United States)

Reid, John B.; Evans, Owen C.; Fates, Dailey G.

1983-12-01

The El Capitan alaskite exposed in the North American Wall, Yosemite National Park, was intruded by two sets of mafic dikes that interacted thermally and chemically with the host alaskite. Comparisons of petrographic and compositional data for these dikes and alaskite with published data for Sierra Nevada plutons lead us to suggest that mafic magmas were important in the generation of the Sierra Nevada batholith. Specifically, we conclude that: (1) intrusion of mafic magmas in the lower crust caused partial melting and generation of alaskite (rhyolitic) magmas; (2) interaction between the mafic and felsic magmas lead to the observed linear variation diagrams for major elements; (3) most mafic inclusions in Sierra Nevada plutons represent chilled pillows of mafic magmas, related by fractional crystallization and granitoid assimilation, that dissolve into their felsic host and contaminate it to intermediate (granodioritic) compositions; (4) vesiculation of hydrous mafic magma upon chilling may allow buoyant mafic inclusions and their disaggregation products to collect beneath a pluton's domed ceiling causing the zoning (mafic margins-to-felsic core) that these plutons exhibit.

Degassing of CO2, SO2, and H2S associated with the 2009 eruption of Redoubt Volcano, Alaska

Science.gov (United States)

Werner, Cynthia A.; Kelly, Peter; Doukas, Michael P.; Lopez, Taryn; Pfeffer, Melissa; McGimsey, Robert G.; Neal, Christina

2013-01-01

The 2009 eruption of Redoubt Volcano, Alaska was particularly well monitored for volcanic gas emissions. We report 35 airborne measurements of CO2, SO2, and H2S emission rates that span from October 2008 to August 2010. The magmatic system degassed primarily as a closed system although minor amounts of open system degassing were observed in the 6 months prior to eruption on March 15, 2009 and over 1 year following cessation of dome extrusion. Only 14% of the total CO2 was emitted prior to eruption even though high emissions rates (between 3630 and 9020 t/d) were observed in the final 6 weeks preceding the eruption. A minor amount of the total SO2 was observed prior to eruption (4%), which was consistent with the low emission rates at that time (up to 180 t/d). The amount of the gas emitted during the explosive and dome growth period (March 15–July 1, 2009) was 59 and 66% of the total CO2and SO2, respectively. Maximum emission rates were 33,110 t/d CO2, 16,650 t/d SO2, and 1230 t/d H2S. Post-eruptive passive degassing was responsible for 27 and 30% of the total CO2 and SO2, respectively. SO2 made up on average 92% of the total sulfur degassing throughout the eruption. Magmas were vapor saturated with a C- and S-rich volatile phase, and regardless of composition, the magmas appear to be buffered by a volatile composition with a molar CO2/SO2 ratio of ~ 2.4. Primary volatile contents calculated from degassing and erupted magma volumes range from 0.9 to 2.1 wt.% CO2 and 0.27–0.56 wt.% S; whole-rock normalized values are slightly lower (0.8–1.7 wt.% CO2 and 0.22–0.47 wt.% S) and are similar to what was calculated for the 1989–90 eruption of Redoubt. Such contents argue that primary arc magmas are rich in CO2 and S. Similar trends between volumes of estimated degassed magma and observed erupted magma during the eruptive period point to primary volatile contents of 1.25 wt.% CO2 and 0.35 wt.% S. Assuming these values, up to 30% additional

Thermal evolution of magma reservoirs in the shallow crust and incidence on magma differentiation: the St-Jean-du-Doigt layered intrusion (Brittany, France)

Science.gov (United States)

Barboni, M.; Bussy, F.; Ovtcharova, M.; Schoene, B.

2009-12-01

Understanding the emplacement and growth of intrusive bodies in terms of mechanism, duration, thermal evolution and rates are fundamental aspects of crustal evolution. Recent studies show that many plutons grow in several Ma by in situ accretion of discrete magma pulses, which constitute small-scale magmatic reservoirs. The residence time of magmas, and hence their capacities to interact and differentiate, are controlled by the local thermal environment. The latter is highly dependant on 1) the emplacement depth, 2) the magmas and country rock composition, 3) the country rock thermal conductivity, 4) the rate of magma injection and 5) the geometry of the intrusion. In shallow level plutons, where magmas solidify quickly, evidence for magma mixing and/or differentiation processes is considered by many authors to be inherited from deeper levels. We show however that in-situ differentiation and magma interactions occurred within basaltic and felsic sills at shallow depth (0.3 GPa) in the St-Jean-du-Doigt bimodal intrusion, France. Field evidence coupled to high precision zircon U-Pb dating document progressive thermal maturation within the incrementally built laccolith. Early m-thick mafic sills are homogeneous and fine-grained with planar contacts with neighbouring felsic sills; within a minimal 0.5 Ma time span, the system gets warmer, adjacent sills interact and mingle, and mafic sills are differentiating in the top 40 cm of the layer. Rheological and thermal modelling show that observed in-situ differentiation-accumulation processes may be achieved in less than 10 years at shallow depth, provided that (1) the differentiating sills are injected beneath consolidated, yet still warm basalt sills, which act as low conductive insulating screens, (2) the early mafic sills accreted under the roof of the laccolith as a 100m thick top layer within 0.5 My, and (3) subsequent and sustained magmatic activity occurred on a short time scale (years) at an injection rate of ca. 0

Effect of inorganic salts on the volatility of organic acids.

Science.gov (United States)

Häkkinen, Silja A K; McNeill, V Faye; Riipinen, Ilona

2014-12-02

Particulate phase reactions between organic and inorganic compounds may significantly alter aerosol chemical properties, for example, by suppressing particle volatility. Here, chemical processing upon drying of aerosols comprised of organic (acetic, oxalic, succinic, or citric) acid/monovalent inorganic salt mixtures was assessed by measuring the evaporation of the organic acid molecules from the mixture using a novel approach combining a chemical ionization mass spectrometer coupled with a heated flow tube inlet (TPD-CIMS) with kinetic model calculations. For reference, the volatility, i.e. saturation vapor pressure and vaporization enthalpy, of the pure succinic and oxalic acids was also determined and found to be in agreement with previous literature. Comparison between the kinetic model and experimental data suggests significant particle phase processing forming low-volatility material such as organic salts. The results were similar for both ammonium sulfate and sodium chloride mixtures, and relatively more processing was observed with low initial aerosol organic molar fractions. The magnitude of low-volatility organic material formation at an atmospherically relevant pH range indicates that the observed phenomenon is not only significant in laboratory conditions but is also of direct atmospheric relevance.

Genesis of felsic plutonic magmas and their igneous enclaves