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  • Artikel: DFG Deutsche Nationallizenzen  (21)
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  • Artikel: DFG Deutsche Nationallizenzen  (21)
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  • 1
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Science Inc
    Journal of metamorphic geology 20 (2002), S. 0 
    ISSN: 1525-1314
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Geologie und Paläontologie
    Notizen: Eclogite facies carbonate rocks have been discovered associated with the granulite–eclogite transitional rocks within Bergen Arc system, Caledonian Orogen of western Norway. The local occurrences of marbles and calc-silicates are found subparallel to the mafic eclogite facies shear zones on Holsnøy Island. Marbles contain the assemblage calcite (Ca0.99Sr0.01CO3), calcian strontianite (Ca0.18−0.44Sr0.53−0.84CO3), clinopyroxene (Jd7−32), epidote/allanite (Ps0−33), titanite, garnet (Alm52−56Grs28−33Pyp11−16), barite (Ba0.90−0.99Sr0.01−0.10SO4), celestine (Sr0.67−0.98Ba0.01−0.23Ca0.01−0.11SO4), and one apparently homogeneous grain of intermediate composition (Ba0.49Ca0.01Sr0.50SO4). Adjacent eclogites have clinopyroxene with similar jadeite contents (Jd14−34) and similar garnet (Alm51−60Grs26−36Pyp8−14) compositions. The marbles have high contents of Sr (9500–11000 p.p.m) and Y (115–130 p.p.m). However, low concentrations of some key trace elements (110–160 p.p.m. Ba and 〈5 p.p.m. Nb) appear to indicate that the marble is not a metamorphosed carbonatite. The 87Sr/86Sr ratios range from 0.7051 to 0.7059. Field and petrological relationships suggest that metasomatic reactions and fluids played a significant role in producing and/or modifying the marbles. The breakdown of scapolite in the granulite into carbonates and sulphates during eclogite facies metamorphism may have contributed to the metasomatic formation of the marbles along shear zones.Fluids involved during subduction are an important catalyst for metamorphism and are recognized to have played a critical role in the localized transformation from granulite to eclogite in the Holsnøy Island area. Thermobarometry indicates 640–690 °C and 18–20 kbar for adjacent eclogites and temperatures of 580–650 °C for the calc-silicates. The marble assemblages are consistent with fluid that is dominantly comprised of H2O (XCO2 〈 0.03) under high-pressure conditions. Phase equilibria of the marbles constrain the fO2 of the fluids and imply oxidizing conditions of the deep crustal fluids. At present the source of the fluids remains unresolved. The results provide additional insights into the variable and evolving nature of fluids related to subduction and high-pressure metamorphism.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Science Inc
    Journal of metamorphic geology 18 (2000), S. 0 
    ISSN: 1525-1314
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Geologie und Paläontologie
    Notizen: Semi-pelitic rocks ranging in grade from the prehnite–pumpellyite to the greenschist facies from south-eastern Otago, New Zealand, have been investigated in order to evaluate the reactions leading to formation and breakdown of stilpnomelane. Detrital grains of mica and chlorite along with fine-grained authigenic illite and chlorite occur in lower-grade rocks with compactional fabric parallel to bedding. At higher grades, detrital grains have undergone dissolution, and metamorphic phyllosilicates have crystallized with preferred orientation (sub)parallel to bedding, leading to slaty cleavage. Stilpnomelane is found in metapelites of the pumpellyite–actinolite facies and the chlorite zone of the greenschist facies, but only rarely in the biotite zone of the greenschist facies. Illite or phengite is ubiquitous, whereas chlorite occurs only rarely with stilpnomelane upgrade of the pumpellyite-out isograd. Chemical and textural relationships suggest that stilpnomelane formed from chlorite, phengite, quartz, K-feldspar and iron oxides. Stilpnomelane was produced by grain-boundary replacement of chlorite and by precipitation from solution, overprinting earlier textures. Some relict 14 Å chlorite layers are observed by TEM to be in the process of transforming to 12 Å stilpnomelane layers. The AEM analyses show that Fe is strongly partitioned over Mg into stilpnomelane relative to chlorite (KD≈2.5) and into chlorite relative to phengite (KD≈1.9). Modified A′FM diagrams, projected from the measured phengite composition rather than from ideal KAl3Si3O10(OH)2, are used to elucidate reactions among chlorite, stilpnomelane, phengite and biotite. In addition to pressure, temperature and bulk rock composition, the stilpnomelane-in isograd is controlled by variations in K, Fe3+/Fe2+, O/OH and H2O contents, and the locus of the isograd is expected to vary in rocks of different oxidation states and permeabilities. Biotite, quartz and less phengitic muscovite form from stilpnomelane, chlorite and phengite in the biotite zone. Projection of bulk rock compositions from phengite, NaAlO2, SiO2 and H2O reveals that they lie close to the polyhedra defined by the A′FM minerals and albite. Other extended A′FM diagrams, such as one projected from phengite, NaAlO2, CaAl2O4, SiO2 and H2O, may prove useful in the evaluation of other low-grade assemblages.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Journal of metamorphic geology 3 (1985), S. 0 
    ISSN: 1525-1314
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Geologie und Paläontologie
    Notizen: Abstract Chemical analysis (including H2, F2, FeO, Fe2O3) of a Mg-vesuvianite from Georgetown, Calif., USA, yields a formula, Ca18.92Mg1.88Fe3+0.40Al10.97Si17.81- O69.0.1(OH)8.84F0.14, in good agreement on a cation basis with the analysis reported by Pabst (1936). X-ray and electron diffraction reveal sharp reflections violating the space group P4/nnc as consistent with domains having space groups P4/n and P4nc. Refinement of the average crystal structure in space group P4/nnc is consistent with occupancy of the A site with Al, of the half-occupied B site by 0.8 Mg and 0.2 Fe, of the half-occupied C site by Ca, of the Ca (1,2,3) sites by Ca, and the OH and O(10) sites by OH and O. We infer an idealized formula for Mg-vesuvianite to be Ca19Mg(MgAl7)Al4Si18O69(OH)9, which is related to Fe3+-vesuvianite by the substitutions Mg + OH = Fe3++ O in the B and O(10) sites and Fe3+= Al in the AlFe site.Thermodynamic calculations using this formula for Mg-vesuvianite are consistent with the phase equilibria of Hochella, Liou, Keskinen & Kim (1982) but inconsistent with those of Olesch (1978). Further work is needed in determining the composition and entropy of synthetic vs natural vesuvianite before quantitative phase equilibria can be dependably generated. A qualitative analysis of reactions in the system CaO-MgO-Al2O3-SiO2-H2O-CO2 shows that assemblages with Mg-vesuvianite are stable to high T in the absence of quartz and require water-rich conditions (XH2O 〉 0.8). In the presence of wollastonite, Mg-vesuvianite requires very water-rich conditions (XH2O 〉 0.97).
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Journal of metamorphic geology 10 (1992), S. 0 
    ISSN: 1525-1314
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Geologie und Paläontologie
    Notizen: The Whitestone Anorthosite (WSA), located in the Central Gneiss Belt of the south-western Grenville Province, Ontario, exhibits a nearly concentric metamorphic envelope characterized by an increase in modal scapolite, hornblende, epidote and garnet, developed around a core of granulite facies clinopyroxene ± orthopyroxene ± garnet meta-anorthosite. Scapolite- and hornblende-bearing assemblages develop mainly at the expense of plagioclase and pyroxene within the envelope.Stable isotopic and petrological data for scapolite-bearing mineral assemblages within meta-anorthosite constrain the source of carbon responsible for CO3-scapolite formation and the extent of fluid/rock interaction between the anorthosite and adjacent lithologies. Stable isotopic data indicate increasing δ18O and δ13C from core to margin of the meta-anorthosite and for samples from the southern extension of the WSA, where it is ductilely deformed within the Parry Sound Shear Zone (PSSZ). The average δ18OSMOW value (whole rock) for the WSA core is 6.9‰, increasing to 11.5‰ where the WSA is in tectonic contact with marble breccia. The average δ13CPBD value of scapolite in meta-anorthosite from the centre of the WSA is -3.4‰, increasing to -0.5‰ at the eastern (marble) contact. Average values of δ13C for scapolite and whole-rock δ18O for samples from the shear zone are -1.0 and 8.0‰, respectively. Marbles have average δ18O and δ13C values of 19.2 and -0.4‰, respectively.The sulphate content of texturally primary scapolite decreases from the core of the WSA (XSO4= 0.48) to the eastern contact (≤0.05). Texturally late scapolite after plagioclase and garnet tends to be CO3-rich relative to texturally primary scapolite, and some scapolite grains show zoning in the anion site with CO3-enriched rims. Scapolite composition may vary at any scale from a single grain to outcrop.The pattern of isotopic enrichment in 13C and 18O preserved in the eastern margin of the WSA is consistent with marble as the major source of fluid contributing to the formation of the metamorphic envelope. The decrease in XSO4 and increase in XCO3 in scapolite toward the margin of the WSA indicate that the volatile content was reset by, or developed from, a CO2-bearing fluid. Assuming derivation of fluid from marble, minimum fluid/rock values at the margin of the WSA range from 0.03 for the least enriched, to 0.30 for the most isotopically enriched samples. Although marble is not found in immediate contact with samples of sheared meta-anorthosite from the PSSZ, a marble source is also consistent with the C and O isotope composition and anion chemistry of scapolite within these samples.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Science Inc
    Journal of metamorphic geology 21 (2003), S. 0 
    ISSN: 1525-1314
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Geologie und Paläontologie
    Notizen: Abstract The prograde metamorphism of eclogites is typically obscured by chemical equilibration at peak conditions and by partial requilibration during retrograde metamorphism. Eclogites from the Eastern Blue Ridge of North Carolina retain evidence of their prograde path in the form of inclusions preserved in garnet. These eclogites, from the vicinity of Bakersville, North Carolina, USA are primarily comprised of garnet–clinopyroxene–rutile–hornblende–plagioclase–quartz. Quartz, clinopyroxene, hornblende, rutile, epidote, titanite and biotite are found as inclusions in garnet cores. Included hornblende and clinopyroxene are chemically distinct from their matrix counterparts. Thermobarometry of inclusion sets from different garnets record different conditions. Inclusions of clinozoisite, titanite, rutile and quartz (clinozoisite + titanite = grossular + rutile + quartz + H2O) yield pressures (6–10 kbar, 400–600 °C and 8–12 kbar 450–680 °C) at or below the minimum peak conditions from matrix phases (10–13 kbar at 600–800 °C). Inclusions of hornblende, biotite and quartz give higher pressures (13–16 kbar and 630–660 °C). Early matrix pyroxene is partially or fully broken down to a diopside–plagioclase symplectite, and both garnet and pyroxene are rimmed with plagioclase and hornblende. Hypersthene is found as a minor phase in some diopside + plagioclase symplectites, which suggests retrogression through the granulite facies. Two-pyroxene thermometry of this assemblage gives a temperature of c. 750 °C. Pairing the most Mg-rich garnet composition with the assemblage plagioclase–diopside–hypersthene–quartz gives pressures of 14–16 kbar at this temperature. The hornblende–plagioclase–garnet rim–quartz assemblage yields 9–12 kbar and 500–550 °C. The combined P–T data show a clockwise loop from the amphibolite to eclogite to granulite facies, all of which are overprinted by a texturally late amphibolite facies assemblage. This loop provides an unusually complete P–T history of an eclogite, recording events during and following subduction and continental collision in the early Palaeozoic.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Contributions to mineralogy and petrology 98 (1988), S. 490-501 
    ISSN: 1432-0967
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie
    Notizen: Abstract The oxygen isotope ratios of various minerals were measured in a granulite-grade iron formation in the Wind River Range, Wyoming. Estimates of temperature and pressure for the terrane using well calibrated geothermometers and geobarometers are 730±50° C and 5.5±0.5 kbar. The mineral constraints on fluid compositions in the iron formation during retrogression require either very CO2-rich fluids or no fluid at all. In the iron formation, isotopic temperature estimates from quartz-magnetite fractionations are controlled by the proximity to the enclosing granitic gneiss, and range from 500° C (Δ qz − mt=10.0‰) within 2–3 meters of the orthogneiss contact to 600° C (Δ qz − mt=8.0‰) farther from the contact. Temperature estimates from other isotopic thermometers are in good agreement with those derived from the quartz-magnetite fractionations. During prograde metamorphism, the isotopic composition of the iron formation was lowered by the infiltration of an external fluid. Equilibrium was achieved over tens of meters. Closed-system retrograde exchange is consistent with the nearly constant whole-rock δ 18Owr value of 8.0±0.6‰. The greater Δ qz-mt values in the iron formation near the orthogneiss contact are most likely due to a lower oxygen blocking temperature related to greater exchange-ability of deformed minerals at the contact. Cooling rates required to preserve the quartz-magnetite fractionations in the central portion of the iron formation are unreasonably high (∼800° C/Ma). In order to preserve the 600° C isotopic temperature, the diffusion coefficient D (for α-quartz) should be two orders of magnitude lower than the experimentally determined value of 2.5×10−16 cm2/s at 833 K. There are no values for the activation energy (Q) and pre-exponential diffusion coefficient (D 0), consistent with the experimentally determined values, that will result in reasonable cooling rates for the Wind River iron formation. The discrepancy between the diffusion coefficient inferred from the Wind River terrane and that measured experimentally is almost certainly due to the enhancement of exchange by the presence of water in the laboratory experiments. Cooling rate estimates were also determined for iron formation retrograded under water-rich conditions. Application of the experimentally determined data to these rocks results in a reasonable cooling rate estimate, supporting the conclusion that the presence of water greatly enhances oxygen diffusion.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    [s.l.] : Nature Publishing Group
    Nature 347 (1990), S. 133-134 
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] HAYOB ETAL. REPLY - Harley and Harte and Barnicoat question our inference that granulite-facies paragneiss xenoliths from Quaternary eruptions in central Mexico preserve the highest regional metamor-phic temperatures yet recorded in deep-seated crustal rocks. Elsewhere, Harley2 has compiled P- T ...
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    [s.l.] : Nature Publishing Group
    Nature 342 (1989), S. 265-268 
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] So far most studies of xenoliths have focused on characterization of samples from the Earth's upper mantle6, and only limited mineralogical and geochemical data have been obtained on xenoliths believed to be from the lower crust. In addition, most studies of deep crustal xenoliths have concentrated ...
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    [s.l.] : Nature Publishing Group
    Nature 301 (1983), S. 226-228 
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] Fig. 1 Dehydration equilibria for synthetic tremolite2 for *H2o = 0.1, 0.25, 0.50, 0.75 and 1.0. We have found a series of metasediments containing enstatite and diopside located at Wolf Hill (JM/TRD) and Burnham Mountain (ST14) in the south-east Indian Lake Quadrangle in the Adirondack ...
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Springer
    Contributions to mineralogy and petrology 100 (1988), S. 92-106 
    ISSN: 1432-0967
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie
    Notizen: Abstract Recently published thermodynamic and experimental data in a variety of chemical systems have been evaluated to derive Gibbs free energies for hedenbergite and pyrope. These were used to calculate the geobarometric equilibria Hedenbergite+Anorthite=Grossular+Almandine +Quartz: “HD barometer”, Diopside+Anorthite=Grossular+Pyrope+Quartz: “DI barometer”. We have compared the pressures obtained from these equilibria for garnet-clinopyroxene-orthopyroxene-plagioclasequartz assemblages with the geobarometer Ferrosilite+Anorthite=Almandine+Grossular+Quartz: “FS barometer”. Pressures calculated for 68 samples containing the above assemblage from a variety of high grade metamorphic terranes indicate that, in general, the HD and DI barometers yield values that are in good agreement with the FS barometer, and that the three barometers are generally consistent with constraints from aluminosilicate occurrences. However, in some samples the HD barometer yields pressures up to 2 kbar greater than constraints imposed by the presence of an aluminosilicate phase. Relative to the FS barometer, the HD barometer overestimates pressure by an average of 0.2±1.0 (1σ) kbar and the DI barometer underestimates pressure by an average of 0.6±1.6 (1σ) kbar. The pressure discrepancies for the HD and DI barometers are likely to be a result of imprecision in thermodynamic data and activity models for silicates, and not a result of resetting of the clinopyroxene equilibria. The relative imprecision of the DI barometer relative to the FS barometer results from overestimates of pressure by the DI and FS barometers in Fe-rich and Mg-rich systems, respectively. Application of the HD and DI barometers to high grade Cpx-Gt-Pg-Qz assemblages yields pressures that are generally consistent with other petrologic constraints and geobarometers. It is concluded that the HD and DI barometers can place reasonable constraints on pressure (±1 kbar relative to the FS barometer) if not extrapolated to mineral assemblages whose compositions are extremely far removed from the end member system for which the barometers were calibrated.
    Materialart: Digitale Medien
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