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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International journal of earth sciences 80 (1991), S. 225-231 
    ISSN: 1437-3262
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Abstract New results obtained by the investigation of liquidus and solidus phase relationships in the haplogranite system Qz-Ab-Or are used to discuss the evolution of magmas during their ascent in the crust. It is assumed that the magmas are formed at 720°C, 820°C, 920°C and at a depth corresponding to a pressure of 8 kbar. The starting composition of the magma is taken as 50% melt plus 50% quartz and feldspars. In case of a closed system (no heat exchange and no transfer of elements) the melt fraction of magmas, the water activity and the viscosity increase with decreasing pressure. The temperature slightly decreases. At 700°C the viscosity is approximatively 2 orders of magnitude lower than at 900°C. This is related to the higher amount of water in the (H2O-undersaturated) melt at low T. It is also shown that dehydration melting is only realistic at high T (900°C). At lower temperatures water has to be added from outside to obtain an intrusive magma with approximatively 50% melt.
    Abstract: Résumé L'évolution des magmas granitiques au cours de leur ascension dans la croûte est discutée à la lumière de données nouvelles relatives aux relations entre phases liquides et solides dans le système Q-Ab-Or. On suppose que les magmas se forment à des températures de 720°C, 820°C, 920°C et à une profondeur correspondant à une pression de 8 Kb. On admet pour leur composition initiale un mélange de 50% de liquide et 50% de quartz + feldspaths. Dans le cas d'un système fermé (pas d'échange de chaleur ni de matière), la fraction liquide du magma, l'activité de l'eau et la viscosité augmentent quand la pression diminue; en même temps, la température décroît légèrement. A 700°C, la viscosité est d'environ 2 ordres de grandeur plus basse qu'à 900°C. Cette propriété est en relation avec la teneur en eau plus élevée dans le liquide (sous-saturé en eau) à basse température. On peut également montrer qu'une fusion déshydratante n'est vraisemblable qu'à haute température (900°C). Aux températures plus basses, de l'eau doit être apportée de l'extérieur pour l'obtention d'un magma à 50% de liquide.
    Notes: Zusammenfassung Neue Ergebnisse, erzielt durch Untersuchungen von Liquidus und Solidus Phasenbeziehungen des Granitsystems Qz-Ab-Or, werden benutzt, um die Entwicklung eines granitoiden Magmas während seines Aufstiegs zu diskutieren. Es wird vorausgesetzt, daß die Magmen bei Temperaturen von 720°C, 820°C und 920°C gebildet werden, sowie in einer Tiefe die einem Druck von 8 kbar entspricht. Die anfängliche Zusammensetzung des Magmas wird mit einem Verhältnis von 50% Schmelze sowie 50% Quarz und Feldspäten angenommen. Im Falle eines geschlossenen Systems (kein Austausch von Wärme und Elementen) steigt die Teilschmelzbildung von Magmen, die Aktivität des Wassers und die Viskosität bei abnehmenden Druck; hierbei sinkt die Temperatur leicht. Bei 700°C ist die Viskosität um ca. 2 Größenordnungen geringer als bei 900°C. Dies wird bedingt durch den höheren Gehalt an Wasser in der (H2O-untersättigten) Schmelze bei tieferen Temperaturen. Es wird außerdem gezeigt, daß Magmenbildung durch Dehydratation nur bei hohen Temperaturen realistisch ist (900°C). Bei tieferen Temperaturen muß Wasser von außen zugeführt werden um ein intrusives Magma zu erhalten, das ungefähr 50% Schmelze besitzt.
    Type of Medium: Electronic Resource
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  • 2
    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.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 130 (1998), S. 213-224 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Liquidus phase relations have been experimentally determined in the systems Qz-Ab-Or-(H2O), Qz-Ab-(H2O) and Qz-Or-(H2O) at H2O-undersaturated conditions (a H2O = 0.07) and P = 5 kbar. Starting materials were homogeneous synthetic glasses containing 1 wt% H2O. The liquidus temperatures were bracketed by crystallization and dissolution experiments. The results of kinetic studies showed that crushed glasses are the best starting materials to overcome undercooling and to minimize the temperature difference between the lowest temperature of complete dissolution (melting) and the highest temperature at which crystallization can be observed. At P = 5 kbar and a H2O = 0.07, the Qz-Ab eutectic composition is Qz32Ab68 at 1095 °C (±10 °C) and the Qz-Or eutectic is Qz38Or62 at 1030 °C (±10 °C). The minimum temperature of the ternary system Qz-Ab-Or is 990 °C (±10 °C) and the minimum composition is Qz32Ab35‐ Or33. The Qz content of the minimum composition in the system Qz-Ab-Or-H2O remains constant with changing a H2O. The normative Or content, however, increases by approximately 10 wt% with decreasing a H2O from 1 to 0.07. Such an increase has already been observed in the system Qz-Ab-Or-H2O-CO2 at high a H2O and it is concluded that the use of CO2 to reduce water activities does not influence the composition of the minima in quartz-feldspar systems. The determined liquidus temperature in melts with 1 wt% H2O is very similar to that obtained in previous nominally “dry” experiments. This discrepancy is interpreted to be due to problems in obtaining absolutely dry conditions. Thus, the hitherto published solidus and liquidus temperatures for “dry” conditions are probably underestimated.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 138 (2000), S. 337-347 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract A review of published and newly measured densities for 40 hydrous silicate glasses indicates that the room-temperature partial molar volume of water is 12.0 ± 0.5 cm3/mol. This value holds for simple or mineral compositions as well as for complex natural glasses, from rhyolite to tephrite compositions, prepared up to 10–20 kbar pressures and containing up to 7 wt% H2O. This volume does not vary either with the molar volume of the water-free silicate phase, with its degree of polymerization or with water speciation. Over a wide range of compositions, this constant value implies that the volume change for the reaction between hydroxyl ions and molecular water is zero and that, at least in glasses, speciation does not depend on pressure. Consistent with data from Ochs and Lange (1997, 1999), systematics in volume expansion for SiO2–M2O systems (M=H, Li, Na, K) suggests that the partial molar thermal expansion coefficient of H2O is about 4 × 10−5 K−1 in silicate glasses.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 113 (1993), S. 492-501 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The effects of F, B2O3 and P2O5 on the H2O solubility in a haplogranite liquid (36 wt. % SiO2, 39 wt. % NaAlSi3O8, 25 wt. % KAlSi3O8) have been determined at 0.5, 1, 2, and 3 kb and 800, 850, and 900°C. The H2O solubility increases with increasing F and B content of the melt. The H2O solubility increase in more important at high pressure (2 and 3 kb) than at low pressure (0.5 kb). At 2 kb and 800°C, the H2O solubility increases from 5.94 to 8.22 wt. % H2O with increasing F content in the melt from 0 to 4.55 wt. %, corresponding to a linear H2O solubility increase of 0.53 mol H2O/mol F. With addition of 4.35 wt. % B2O3, the H2O solubility increases up to 6.86 wt. % H2O at 2 kb and 800°C, corresponding to a linear increase of 1.05 mol H2O/mol B2O3. The results allow to define the individual effects of fluorine and boron on H2O solubility in haplogranitic melts with compositions close to that of H2O-saturated thermal minima (at 0.5–3 kb). Although P has a dramatic effect on the phase relations in the haplogranite system, its effect on the H2O solubility was found to be negligible in natural melt compositions. The concominant increase in H2O solubility and F can not be interpreted on the basis of the available spectroscopic data (existence of hydrated aluminofluoride complexes or not). In contrast, hydrated borates or more probably boroxol complexes have been demonstrated in B-bearing hydrous melts.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 136 (1999), S. 213-224 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The water solubility in haplogranitic melts (normative composition Ab39Or32Qz29) coexisting with H2O-H2 fluids at 800 and 950 °C and 1, 2 and 3 kbar vapour pressure has been determined using IR spectroscopy. The experiments were performed in internally heated pressure vessels and the hydrogen fugacity (f H2) was controlled using the double capsule technique and oxygen buffer assemblages (WM and IW). Due to the limited lifetimes of these oxygen buffers the water solubility was determined from diffusion profiles (concentration-distance profiles) measured with IR spectroscopy in the quenched glasses. The reliability of the experimental strategy was demonstrated by comparing the results of short- and long-duration experiments performed with pure H2O fluids. The water solubility in Ab39Or32Qz29 melts equilibrated with H2O-H2 fluids decreases progressively with decreasing f H2O, as f H2 (or X H2) increases in the fluid phase. The effect of H2 on the evolution of the water solubility is similar to that of CO2 or another volatile with a low solubility in the melt and can be calculated in a first approximation with the Burnham water solubility model. Recalculation of high temperature water speciation for AOQ melts coexisting with H2O-H2 fluids at 800 °C, 2 kbar suggests that the concentrations of molecular H2O are proportional to f H2O (calculated using available mixing models), indicating Henrian behaviour for the solubility of molecular H2O in haplogranitic melts.
    Type of Medium: Electronic Resource
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