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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillian Magazines Ltd.
    Nature 410 (2001), S. 197-200 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The low concentrations of niobium, tantalum and titanium observed in island-arc basalts are thought to result from modification of the sub-arc mantle by a metasomatic agent, deficient in these elements, that originates from within the subducted oceanic crust. Whether this agent is an hydrous ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 430 (2004), S. 0 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Arising from: A. E. Saal, E. H. Hauri, C. H. Langmuir & M. R. Perfit Nature 419, 451–455 (2002); Saal et al. replyAssessing the conditions under which magmas become fluid-saturated has important ...
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 445 (2007), S. 194-197 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Volatiles carried by magmas, either dissolved or exsolved, have a fundamental effect on a variety of geological phenomena, such as magma dynamics and the composition of the Earth’s atmosphere. In particular, the redox state of volcanic gases emanating at the Earth’s surface is ...
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 126 (1997), S. 386-400 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Solidus temperatures of quartz–alkali feldspar assemblages in the haplogranite system (Qz-Ab-Or) and subsystems in the presence of H2O-H2 fluids have been determined at 1, 2, 5 and 8 kbar vapour pressure to constrain the effects of redox conditions on phase relations in quartzofeldspathic assemblages. The hydrogen fugacity (f H2) in the fluid phase has been controlled using the Shaw membrane technique for moderately reducing conditions (f H2 〈 60 bars) at 1 and 2 kbar total pressure. Solid oxygen buffer assemblages in double capsule experiments have been used to obtain more reducing conditions at 1 and 2 kbar and for all investigations at 5 and 8 kbar. The systems Qz-Or-H2O-H2 and Qz-Ab-H2O-H2 have only been investigated at moderately reducing conditions (1 and 5 kbar) and the system Qz-Ab-Or-H2O-H2 has been investigated at redox conditions down to IW (1 to 8 kbar). The results obtained for the water saturated solidi are in good agreement with those of previous studies. At a given pressure, the solidus temperature is found to be constant (within the experimental precision of ± 5°C) in the f H2 range of 0–75 bars. At higher f H2, generated by the oxygen buffers FeO-Fe3O4 (WM) and Fe-FeO (IW), the solidus temperatures increase with increasing H2 content in the vapour phase. The solidus curves obtained at 2 and 5 kbar have similar shapes to those determined for the same quartz - alkali feldspar assemblages with H2O-CO2- or H2O-N2-bearing systems. This suggests that H2 has the behaviour of an inert diluent of the fluid phase and that H2 solubility in aluminosilicate melts is very low. The application of the results to geological relevant conditions [HM (hematite-magnetite) 〉 f O2 〉 WM] shows that increasing f H2 produces a slight increase of the solidus temperatures (up to 30 °C) of quartz–alkali feldspar assemblages in the presence of H2O-H2 fluids between 1 and 5 kbar total pressure.
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  • 5
    Publication Date: 2012-02-01
    Description: Iron oxidation state and coordination geometry have been determined by Fe K-edge X-ray absorption near edge spectroscopy (XANES) for three sets of silicate glasses of peralkaline rhyolitic composition with different peralkalinity values. These compositions were chosen to investigate the effect of alkali content (and oxygen fugacity) on the Fe oxidation state. The samples were produced by means of hydrothermal vessels at 800 °C with oxygen fugacity conditions ranging from NNO-1.61 to NNO+2.96 log units.Comparison of the pre-edge peak data with those of Fe model compounds of known oxidation state and coordination number allowed determination of the Fe oxidation state and coordination number in all glasses analyzed. Within each group of samples, Fe tends to oxidize with increasing oxygen fugacity as expected. However, alkali content is shown to have a strong effect on the Fe3+/(Fe3++Fe2+) ratio at constant oxygen fugacity: this ratio varies from 0.25 to 0.55 (±0.05) for the least peralkaline series, and from 0.45 to 0.80 (±0.05) for the most peralkaline series. Moreover, pre-edge peak data clearly indicate that Fe3+ is in fourfold coordination in the most peralkaline glasses. Extrapolation of pre-edge peak data suggests the presence of both fourfold and fivefold coordination for trivalent Fe in the other two series. Divalent Fe is suggested to be mainly in fivefold coordination in all the three glass series. The presence of minor amounts of sixfold- and fourfold-coordinated Fe cannot be ruled out by XANES data alone. XANES data suggest that the amount of alkalis also affects the Fe3+ coordination environment resulting in a decrease in the average coordination numbers.Extended X-ray absorption fine structure (EXAFS) data of the most oxidized and peralkaline sample indicate that Fe3+ is in tetrahedral coordination with = 1.85 Å (±0.02). This value compares well with literature data for [4]Fe3+ in crystalline phases (e.g., in tetra-ferriphlogopite or rodolicoite) or in silicate glasses (e.g., phonolite glasses) supporting the XANES-determined coordination number obtained for the most peralkaline glasses.Calculated NBO/T ratios decrease slightly with Fe oxidation because of the higher fraction of network forming Fe, thus increasing the polymerization of the tetrahedral network.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 6
    Publication Date: 2021-01-25
    Description: Peralkaline rhyolites, associated with extensional tectonic settings, are medium to low viscosity magmas that often produce eruptive styles ranging from effusive to highly explosive eruptions. The role of pre-eruptive conditions and crystallization kinetics in influencing the eruptive style of peralkaline rhyolitic magmas has been investigated and debated considering equilibrium conditions. However, experimental constraints on the effect of disequilibrium in crystallization in such magmas are currently lacking in the literature. Therefore, we performed isobaric cooling experiments to investigate alkali feldspar crystallization kinetics in peralkaline rhyolitic melts. Experiments were performed under water-saturated, water-undersaturated, and anhydrous conditions between 25 and 100 MPa, at 670–790◦C and with experimental durations ranging from 0.5 to 420 h. Here we present the first data on crystallization kinetics of alkali feldspar, which is the main crystal phase in peralkaline rhyolitic melts, in order to improve our understanding of the evolutionary timescales of these melts and their ability to shift between effusive and explosive activity. Our experimental results indicate that the alkali feldspar nucleation delay can range from hours to several days as a function of undercooling and H2O content in the melt. Thus, a peralkaline rhyolitic magma can be stored at the pre-eruptive conditions for days without important variations of its crystal fraction. This suggests that crystallization may not necessarily play the main role in triggering fragmentation during explosive eruptions of peralkaline rhyolitic magmas.
    Description: PRIN 2009 (2009PZ47NA_002), FAR2012, PRIN 2017 (2017J277S9 – all MC) and the EU LIFE
    Description: Published
    Description: 177
    Description: 4V. Processi pre-eruttivi
    Description: JCR Journal
    Keywords: alkali feldspar ; peralkaline rhyolite ; nucleation delay ; crystallization kinetics ; Pantelleria volcanic system ; Crystallization Kinetics of Alkali Feldspar ; Peralkaline Rhyolitic Melts
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 7
    Publication Date: 2017-09-11
    Description: characterization of ultra-calcic arc melts, equilibrium phase relations have been determined experimentally for the La Sommata basalt (Som-1, Vulcano, Aeolian arc). Som-1 (Na2O + K2O = 4.46 wt.%, CaO = 12.97 wt.%, MgO = 8.78 wt.%, CaO/Al2O3 = 1.03) is a reference primitive ne-normative arc basalt with a strong ultra-calcic affinity. The experiments have been performed between 44 and 154 MPa, 1050 and 1150 °C and from NNO + 0.2 to NNO + 1.9. Fluid-present conditions were imposed with H2O–CO2 mixtures yielding melt H2O concentrations from0.7 to 3.5wt.%. Phases encountered include clinopyroxene, olivine, plagioclase and Fe-oxide. Clinopyroxene is slightly earlier than olivine in the crystallization sequence. It is the liquidus phase at 150 MPa, being joined by olivine on the liquidus between 44 and 88MPa. Plagioclase is the third phase to appear in the crystallization sequence and orthopyroxene was not found. Experimental clinopyroxenes (Fs7–16) and olivines (Fo78–92) partially reproduce the natural phenocryst compositions (respectively Fs5–7 and Fo87–91). Upon progressive crystallization, experimental liquids shift towards higher SiO2 (up to ~55 wt.%), Al2O3 (up to ~18 wt.%) and K2O (up to ~5.5wt.%) and lower CaO,MgO and CaO/Al2O3. Experimental glasses and natural whole-rock compositions overlap, indicating that progressive crystallization of Som-1 type melts can generate differentiated compositions such as those encountered at Vulcano. The lowpressure cotectic experimental glasses reproduce glass inclusions in La Sommata clinopyroxene but contrast with glass inclusions in olivine which preserve basaltic melts more primitive than Som-1. Phase relations for the La Sommata basalt are identical in all critical aspects to those obtained previously on a synthetic ultra-calcic arc composition. In particular, clinopyroxene+olivine co-saturation occurs at very low pressures (≤100 MPa). Ultra-calcic arc compositions do not represent primary mantle melts but result from the interaction between a primary mantle melt and clinopyroxene-bearing rocks in the arc crust. At Vulcano, primitive ultra-calcic end-member melts were generated between 250 and 350 MPa in the lower magma accumulation zone by reaction between hot primitive melts and wehrlitic or gabbroic lithologies. At Stromboli, golden pumices and glass inclusions with an ultra-calcic affinity were also generated at shallow pressures, between 150 and 250 MPa, suggesting that the interaction model is of general significance in the Aeolian arc.
    Description: Published
    Description: 85-101
    Description: 2V. Struttura e sistema di alimentazione dei vulcani
    Description: JCR Journal
    Keywords: Primitive arc magmas, Ultra-calcic Experiments, Phase equilibria, Vulcano, Aeolian arc ; Petrology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 8
    Publication Date: 2018-09-20
    Description: The relationships between trachytes and peralkaline rhyolites (i.e. pantellerites and comendites), which occur in many continental rift systems, oceanic islands and continental intraplate settings, is unclear. To fill this gap, we have performed phase equilibrium experiments on two representative metaluminous trachytes from Pantelleria to determine both their pre-eruptive equilibration conditions (pressure, temperature, H2O content and redox state) and liquid lines of descent. Experiments were performed in the temperature range 750–950 C, pressure 0 5–1 5 kbar and fluid saturation conditions with XH2O [¼H2O/(H2OþCO2)] ranging between zero and unity. Redox conditions were fixed below the nickel–nickel oxide buffer (NNO). The results show that at 950 C and melt water contents (H2Omelt) close to saturation, trachytes are at liquidus conditions at all pressures. Clinopyroxene is the liquidus phase, being followed by iron-rich olivine and alkali feldspar. Comparison of experimental and natural phases (abundances and compositions) yields the following pre-eruptive conditions: P¼160 5 kbar, T¼925625 C, H2Omelt¼261wt %, and fO2 between NNO– 0 5 and NNO– 2. A decrease in temperature from 950 C to 750 C, as well as of H2Omelt, promotes a massive crystallization of alkali feldspar to over 80 wt %. Iron-bearing minerals show gradual iron enrichment when T and fO2 decrease, trending towards the compositions of the phenocrysts of natural pantellerites. Despite the metaluminous character of the bulk-rock compositions, residual glasses obtained after 80 wt % crystallization evolve toward comenditic compositions, owing to profuse alkali feldspar crystallization, which decreases the Al2O3 of the melt, leading to a consequent increase in the peralkalinity index [PI¼molar (Na2OþK2O)/Al2O3]. This is the first experimental demonstration that peralkaline felsic derivatives can be produced by low-pressure fractional crystallization of metaluminous mafic magmas. Our results show that the pantelleritic magmas of basalt–trachyte–rhyolite igneous suites require at least 95 wt % of parental basalt crystallization, consistent with trace element evidence. Redox conditions, through their effect on Fe–Ti oxide stabilities, control the final iron content of the evolving melt.
    Description: Published
    Description: 559- 588
    Description: 2V. Struttura e sistema di alimentazione dei vulcani
    Description: JCR Journal
    Keywords: peralkaline silicic magmatism ; Pantelleria ; Green Tuff ; petrology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 9
    Publication Date: 2021-11-09
    Description: Volcanogenic halogens, in particular bromine, potentially play an important role in the ozone depletion of the atmosphere. Understanding bromine behaviour in magmas is therefore crucial to properly evaluate the contribution of volcanic eruptions to atmospheric chemistry and their environmental impact. To date, bromine partitioning between silicate melts and the gas phase is very poorly constrained, with the only relevant experimental studies limited to investigation of synthetic melt with silicic compositions. In this study, fluid/melt partitioning experiments were performed using natural silicate glasses with mafic, intermediate and silicic compositions. For each composition, experiments were run with various Br contents in the initial fluid (H2O–NaBr), at T–Pconditions representative of shallow magmatic reservoirs in volcanic arc contexts (100–200MPa, 900–1200◦C). The resulting fluid/melt partition coefficients (DBrf/m) are: 5.0 ±0.3 at 1200◦C–100MPa for the basalt, 9.1 ±0.6 at 1060◦C–200MPa for the andesite and 20.2 ±1.2 at 900◦C–200MPa for the rhyodacite. Our experiments show that DBrf/mincreases with increasing SiO2content of the melt (as for chlorine) and suggest that it is also sensitive to melt temperature (increase of DBrf/mwith decreasing temperature). We develop a simple model to predict the S–Cl–Br degassing behaviour in mafic systems, which accounts for the variability of S–Cl–Br compositions of volcanic gases from Etna and other mafic systems, and shows that coexisting magmatic gas and melt evolve from S-rich to Cl–Br enriched (relative to S) upon increasing degree of degassing. We also report first Br contents for melt inclusions from Etna, Stromboli, Merapi and Santorini eruptions and calculate the mass of bromine available in the magma reservoir prior to the eruptions under consideration. The discrepancy that we highlight between the mass of Br in the co-existing melt and fluid prior to the Merapi 2010 eruption (433 and 73 tons, respectively) and the lack of observed BrO (from space) hints at the need to investigate further Br speciation in ‘ash-rich’ volcanic plumes. Overall, our results suggest that the Br yield into the atmosphere of cold and silicic magmas will be much larger than that from hotter and more mafic magmas.
    Description: Published
    Description: 450-463
    Description: 4V. Processi pre-eruttivi
    Description: JCR Journal
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 10
    Publication Date: 2023-11-21
    Description: Crystallization experiments on two pantellerites from Pantelleria, Italy, provide new evidence for the relationships between mineral phases in pantelleritic rocks aswell as the influence of temperature and redox conditions on mineral assemblages. Experiments were performed at 1 kbar with temperature ranging between 750–900°C, and fluid saturation conditionswith XH2O (=H2O/H2O+CO2) between 0 and 1. Redox conditionswere fixed at, or slightly below, the FMQbuffer. Results showthat at temperature of 900 °C pantelleriticmagmas arewell above the liquidus regardless their water content; we also observed a decrease in liquidus temperature (800°C) with increasingly reducing conditions. Mineral assemblages of the natural rocks have been successfully reproduced, particularly the relationship between fayalite and aenigmatite, which appear to be strongly controlled by melt peralkalinity, temperature and redox conditions. This is the first time that fayalitic olivine have been synthetized in experimental studies on pantellerites, which was found to be stable only for temperatures ≥750°C while amphibole can be stable at temperatures as high as 800°C at high fF2. Experimental results have been compared with the composition of mineral phases as well as with the results obtained from mineral equilibrium, geothermometry, and oxygen barometry studies on pantelleritic lava and tuffs from Pantelleria (Italy), Eburru (Kenya) and Menengai (Kenya). Petrological characteristics appear similar at different locations worldwide, with typical assemblages of anorthoclase and sodian clinopyroxene with variable fayalite, aenigmatite, Fe-Ti oxides and amphibole.
    Description: Published
    Description: 105793
    Description: 4V. Processi pre-eruttivi
    Description: JCR Journal
    Keywords: Pantellerite, Mineral Equilibria, Experimental Petrolog, Peralkaline magmas ; 03.01. General
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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