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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 308 (1984), S. 538-541 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The overall stoichiometry of pyrite oxidation may be described by the reaction: FeS2(s) +15/4O2(aq) +7/2H2O Fe(OH)3(s) + 2H2SO4(aq). In order to understand the oxidation kinetics, intermediate steps in this reaction must be considered1. The following three reactions have been shown to operate ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 442 (2006), S. 908-911 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The presence of mass-independently fractionated sulphur isotopes (MIF-S) in many sedimentary rocks older than ∼2.4 billion years (Gyr), and the absence of MIF-S in younger rocks, has been considered the best evidence for a dramatic change from an anoxic to oxic atmosphere around ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 68 (1979), S. 187-205 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Late Cretaceous, granitic pegmatite-aplite dikes in southern California have been known for gem-quality minerals and as a commercial source of lithium. Minerals, whole-rock samples, and inclusion fluids from nine of these dikes and from associated wall rocks have been analyzed for their oxygen, hydrogen, and carbon isotope compositions to ascertain the origins and thermal histories of the dikes. Oxygen isotope geothermometry used in combination with thermometric data from primary fluid inclusions enabled the determination of the pressure regime during crystallization. Two groups of dikes are evident from their oxygen isotope compositions (δ18Oqtz≃+10.5 in Group A, and ≃+8.5 in Group B). Prior to the end of crystallization, Group A pegmatites had already extensively exchanged oxygen with their wall rocks, while Group B dikes may represent a closer approximation to the original isotopic composition of the pegmatite melts. Oxygen isotope fractionations between minerals are similar in all dikes and indicate that the pegmatites were emplaced at temperatures of about 730 ° to 700 ° C. Supersolidus crystallization began with the basal aplite zone and ended with formation of “quench aplite” in the pocket zone, nearly to 565 ° C. Subsolidus formation of gem-bearing pockets took place over a relatively narrow temperature range of about 40 ° C (approximately 565–525 ° C). Nearly closed-system crystallization is indicated. Hornblende in gabbroic and noritic wall rocks (δDw.r. = −90 to −130) in the Mesa Grande district crystallized in the presence of, or exchanged hydrogen with, meteoric water (δD≃ −90) prior to the emplacement of the pegmatite dikes. Magmatic water was subsequently added to the wall rocks adjacent to the pegmatites. Groups A and B pegmatites cannot be distinguished on the basis of their hydrogen isotope compositions. A decrease in δD of muscovite inward from the walls of the dikes reflects a decrease in temperature. δD values of H2O from fluid inclusions are: −50 to −73 (aplite and pegmatite zones); −62 to −75 (pocket quartz: Tourmaline Queen and Stewart dikes); and −50 ± 4 (pocket quartz from many dikes). The average δ13C of juvenile CO2 in fluid inclusions in Group B pegmatites is −7.9. In Group A pegmatities, δ13C of CO2 is more negative (−10 to −15.6), due to exchange of C with wall rocks and/or loss of 13C-enriched CO2 to an exsolving vapor phase. Pressures during crystallization of the pockets were on the order of 2,100 bars, and may have increased slightly during pocket growth. A depth of formation of at least 6.8 km (sp. gr. of over burden = 3.0, and P fiuid=P load) is indicated, and a rate of uplift of 0.07 cm/yr. follows from available geochronologic data.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 63 (1977), S. 1-49 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Garnet-pyroxene skarns were formed 90 m.y. B.P. in the Osgood Mountains at or near contacts of grandiorite with calcareous rocks of the Cambrian Preble Formation. The metasomatic replacement followed contact metamorphic recrystallization of the Preble. The sources, temperature, and variation in H2O/CO2 ratios of the metasomatic fluid are interpreted from 269 analyses of oxygen, carbon, hydrogen, and sulfur isotopes in whole rocks, minerals and inclusion fluids. Skarns formed in three mineralogical stages. Oxygen isotope data indicate that temperatures during the crystallization of garnet, pyroxene and wollastonite (Stage I) were least 550 ° C, and that the metasomatic fluid had an $${\text{X}}_{{\text{CO}}_{\text{2}} } $$ ≦ 0.035 in the massive skarns, and ≦ 0.12 in vein skarns up to 3 cm thick. Pore fluids in isotopic equilibrium with garnet in calc-silicate metamorphic rocks, on the other hand, had $${\text{X}}_{{\text{CO}}_{\text{2}} } $$ ≦ 0.15. The metasomatic fluids of Stage I were derived primarily from the crystallizing magma. The isotopic composition of magmatic water was δ18O =+9.0, δD= −30 to −45. Oxygen isotope temperatures of greater than 620 ° C were determined for the granodiorite. Isotopic and chemical equilibria between mineral surfaces and the metasomatic fluid were approached simultaneously in parts of the skarn several meters or more apart, while isotopic and chemical disequilibria (i.e. zoning) have been preserved between 20 to 40 μm-thick zones in grandite garnet. More Fe-, or andradite-rich garnet crystallized in more H2O-rich C-O-H fluids ( $${\text{X}}_{{\text{CO}}_{\text{2}} } $$ ≦ 0.01) than present with grossularite-rich garnet ( $${\text{X}}_{{\text{CO}}_{\text{2}} } $$ ≦ 0.035). Stage II was marked by the replacement of garnet and pyroxene by quartz, amphibole, plagioclase, epidote, magnetite, and calcite. Many of the replacement reactions took place over a relatively narrow range in temperature (480–550 ° C), as indicated by 18O fractionations between quartz and amphibole. Meteoric water comprised 20 to 50% of the metasomatic fluid during Stage II. Calcite was formed along with pyrite, minor pyrrhotite, and chalcopyrite during Stage III, although the crystallization of pyrite and calcite had begun earlier, during Stages I and II, respectively. Carbon and sulfur isotope compositions of calcite and pyrite indicate a magmatic source for most of the C and S in the metasomatic fluids of Stage III. By the end of Stage III, meteoric water constituted as much as 100% of the metasomatic fluid. Minerals from grandiorite and skarn do not show large depletions in 18O because the oxygen isotope composition of the metasomatic fluid was buffered by the calcareous wall rocks and the grandiorite. Meteoric water in the vicinity of the Osgood Mountains during the Late Crectaceous (δ18Ocale. ≃ −14.0, δD = − 107) was slightly enriched in 18O and D relative to present-day meteoric water (δ18O = 15.9, δD = − 117)
    Type of Medium: Electronic Resource
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