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Fluid Inclusion Data (fluid + inclusion_data)
Selected AbstractsGeochemical constraints of the eclogite and granulite facies metamorphism as recognized in the Raobazhai complex from North Dabie Shan, ChinaJOURNAL OF METAMORPHIC GEOLOGY, Issue 1 2001Y. L. Xiao Abstract A combined study of major and trace elements, fluid inclusions and oxygen isotopes has been carried out on garnet pyroxenite from the Raobazhai complex in the North Dabie Terrane (NDT). Well-preserved compositional zoning with Na decreasing and Ca and Mg increasing from the core to rim of pyroxene in the garnet pyroxenite indicates eclogite facies metamorphism at the peak metamorphic stage and subsequent granulite facies metamorphism during uplift. A P,T path with substantial heating (from c. 750 to 900 °C) after the maximum pressure reveals a different uplift history compared with most other eclogites in the South Dabie Terrane (SDT). Fluid inclusion data can be correlated with the metamorphic grade: the fluid regime during the peak metamorphism (eclogite facies) was dominated by N2 -bearing NaCl-rich solutions, whereas it changed into CO2 -dominated fluids during the granulite facies retrograde metamorphism. At a late retrograde metamorphic stage, probably after amphibolite facies metamorphism, some external low-salinity fluids were involved. In situ UV-laser oxygen isotope analysis was undertaken on a 7 mm garnet, and impure pyroxene, amphibole and plagioclase. The nearly homogeneous oxygen isotopic composition (,18OVSMOW = c. 6.7,) in the garnet porphyroblast indicates closed fluid system conditions during garnet growth. However, isotopic fractionations between retrograde phases (amphibole and plagioclase) and garnet show an oxygen isotopic disequilibrium, indicating retrograde fluid,rock interactions. Unusual MORB-like rare earth element (REE) patterns for whole rock of the garnet pyroxenite contrast with most ultra-high-pressure (UHP) eclogites in the Dabie-Sulu area. However, the age-corrected initial ,Nd(t) is ,,2.9, which indicates that the protolith of the garnet pyroxenite was derived from an enriched mantle rather than from a MORB source. Combined with the present data of oxygen isotopic compositions and the characteristic N2 content in the fluid inclusions, we suggest that the protolith of the garnet pyroxenite from Raobazhai formed in an enriched mantle fragment, which has been exposed to the surface prior to the Triassic metamorphism. [source] DEVONIAN CARBONATES OF THE NIGEL PEAK AREA, ROCKY MOUNTAINS, CANADA: A FOSSIL PETROLEUM SYSTEM?JOURNAL OF PETROLEUM GEOLOGY, Issue 3 2008J. Köster In this study we report on Devonian (Frasnian , Famennian) limestones and dolostones exposed near Nigel Peak in the Main Ranges of the Canadian Rocky Mountains. These carbonates are a proximal facies of the Southesk-Cairn Carbonate Complex. The investigated strata are stratigraphically equivalent to the oil- and gas bearing Nisku Formation in the subsurface of the Western Canada Sedimentary Basin, about 300 km to the east. The rocks were investigated by polarisation and cathodoluminescence microscopy, total organic carbon analysis, Rock-Eval pyrolysis, solid bitumen reflectance measurements, gas chromatography and fluid inclusion analysis. Thin section analyses showed that silt-grade quartz and saddle dolomite increase upward from the base of the stratigraphic section, and that porosities are generally low. This is due to reduction of pore space due to early cementation and extensive dolomitization. Cathodoluminescence identified up to four generations of calcite cements. TOC values ranged from 0.2 to 2.4 %. Rock-Eval pyrolysis of carbonate samples resulted in measurable S1 peaks but not S2 peaks, indicating that there was no residual petroleum generation potential. Organic petrographic analyses identified dispersed kerogen and migrabitumen, and calculated vitrinite reflectance values were around 4 % on average which implies peak temperatures of 234,262 °C (due to deep burial) or 309,352 °C (due to short term hydrothermal heating). Fluid inclusion data indicates at least one pulse of hot fluids with elevated homogenization temperatures of > 300 °C, and this may explain the high thermal maturity of the studied rocks. [source] Precipitation of lead,zinc ores in the Mississippi Valley-type deposit at Trèves, Cévennes region of southern FranceGEOFLUIDS (ELECTRONIC), Issue 1 2006D. LEACH Abstract The Trèves zinc,lead deposit is one of several Mississippi Valley-type (MVT) deposits in the Cévennes region of southern France. Fluid inclusion studies show that the ore was deposited at temperatures between approximately 80 and 150°C from a brine that derived its salinity mainly from the evaporation of seawater past halite saturation. Lead isotope studies suggest that the metals were extracted from local basement rocks. Sulfur isotope data and studies of organic matter indicate that the reduced sulfur in the ores was derived from the reduction of Mesozoic marine sulfate by thermochemical sulfate reduction or bacterially mediated processes at a different time or place from ore deposition. The large range of ,34S values determined for the minerals in the deposit (12.2,19.2, for barite, 3.8,13.8, for sphalerite and galena, and 8.7 to ,21.2, for pyrite), are best explained by the mixing of fluids containing different sources of sulfur. Geochemical reaction path calculations, based on quantitative fluid inclusion data and constrained by field observations, were used to evaluate possible precipitation mechanisms. The most important precipitation mechanism was probably the mixing of fluids containing different metal and reduced sulfur contents. Cooling, dilution, and changes in pH of the ore fluid probably played a minor role in the precipitation of ores. The optimum results that produced the most metal sulfide deposition with the least amount of fluid was the mixing of a fluid containing low amounts of reduced sulfur with a sulfur-rich, metal poor fluid. In this scenario, large amounts of sphalerite and galena are precipitated, together with smaller quantities of pyrite precipitated and dolomite dissolved. The relative amounts of metal precipitated and dolomite dissolved in this scenario agree with field observations that show only minor dolomite dissolution during ore deposition. The modeling results demonstrate the important control of the reduced sulfur concentration on the Zn and Pb transport capacity of the ore fluid and the volumes of fluid required to form the deposit. The studies of the Trèves ores provide insights into the ore-forming processes of a typical MVT deposit in the Cévennes region. However, the extent to which these processes can be extrapolated to other MVT deposits in the Cévennes region is problematic. Nevertheless, the evidence for the extensive migration of fluids in the basement and sedimentary cover rocks in the Cévennes region suggests that the ore forming processes for the Trèves deposit must be considered equally viable possibilities for the numerous fault-controlled and mineralogically similar MVT deposits in the Cévennes region. [source] Chemical, Isotopic, and Fluid Inclusion Evidence for the Hydrothermal Alteration of the Footwall Rocks of the BIF-Hosted Iron Ore Deposits in the Hamersley District, Western AustraliaRESOURCE GEOLOGY, Issue 2 2003Makoto Haruna Abstract. The petrography, chemical, fluid inclusion and isotope analyses (O, Rb-Sr) were conducted for the shale samples of the Mount McRae Shale collected from the Tom Price, Newman, and Paraburdoo mines in the Hamersley Basin, Western Australia. The Mount McRae Shale at these mines occurs as a footwall unit of the secondary, hematite-rich iron ores derived from the Brockman Iron Formation, one of the largest banded iron formations (BIFs) in the world. Unusually low contents of Na, Ca, and Sr in the shales suggest that these elements were leached away from the shale after deposition. The ,18O (SMOW) values fall in the range of + 15.0 to +17.9 per mil and show the positive correlation with calculated quartz/sericite ratios of the shale samples. This suggests that the oxygen isotopic compositions of shale samples were homogenized and equilibrated by postdepositional event. The pyrite nodules hosted by shales are often rimmed by thin layers of silica of varying crystallinity. Fluid inclusions in quartz crystals rimming a pyrite nodule show homogenization temperatures ranging from 100 to 240d,C for 47 inclusions and salinities ranging from 0.4 to 12.3 wt% NaCl equivalent for 18 inclusions. These fluid inclusion data give direct evidence for the hydrothermal activity and are comparable to those of the vein quartz collected from the BIF-derived secondary iron ores (Taylor et al, 2001). The Rb-Sr age for the Mount McRae Shale is 1,952 ± 289 Ma and at least 200 million years younger than the depositional age of the Brockman Iron Formation of , 2.5 Ga in age. All the data obtained in this study are consistent with the suggestion that high temperature hydrothermal fluids were responsible for both the secondary iron ore formation and the alteration of the Mount McRae Shale. [source] Mineral Paragenesis and Fluid Inclusions of Some Pluton-hosted Vein-type Copper Deposits in the Coastal Cordillera, Northern ChileRESOURCE GEOLOGY, Issue 1 2003Dania Trista Abstract. Formation conditions of some vein-type copper deposits of the Tocopilla district (Deseada, San Jose, Santa Rosa) and the Gatico district (Yohanita, Toldo-Velarde, Argentina) in the Coastal Cordillera of northern Chile were inferred from mineral paragenesis and fluid inclusion data, and were compared with those of neighboring stratiform copper deposits. The vein-type copper deposits are hosted in Late Jurassic dioritic to quartz-dioritic plutons intruding extensively an andesite-dominant volcanic pile of the Jurassic La Negra Formation. Primary mineralization is characterized by chalcopyrite + magnetite + pyrite + bornite, and supergene alteration of these minerals produced anilite, covellite, atacamite and chrysocolla. The hypogene mineral assemblage indicates relatively high sulfur fugacity and weakly oxidized conditions, distinct from the stratiform copper deposits formed under low sulfur fugacity and moderately oxidized conditions. Furthermore, the fluid inclusion data of the vein-type deposits indicate high temperature (401,560d,C) and high salinity (39,68 wt% NaCl equiv.) ranges in contrast to the stratiform deposits, suggesting that this type of deposits formed by magma-associated hypersaline ore fluids. [source] Mineralogy, Geochemistry, and Age Constraints on the Beni Bou Ifrour Skarn Type Magnetite Deposit, Northeastern MoroccoRESOURCE GEOLOGY, Issue 1 2002Mohammed EL RHAZI Abstract: The Beni Bou Ifrour deposit of northeastern Morocco is a skarn type magnetite deposit. K-Ar age determination suggests that the mineralization occurred at 7.040.47 Ma. The spatial relationship between skarn and dikes of microgran-odiorite derived from the batholith of Wiksane Granodiorite, and the similarity of age (8.020.22 Ma), confirms that the Wiksane Granodiorite is the igneous rock most probably related to mineralization. The skarn is distributed asymmetrically in the limestone, and magnetite ore was developed just below the calc-silicate skarn as two parallel beds separated by 100 m of barren limestone and schist. The mineralization can be divided into three stages. The early stage is characterized by the formation of calc-silicate minerals, mainly clinopyroxene (80,70 % diopside) and garnet (early almost pure andradite to the late 60 % andradite). The main stage is characterized by the formation of a large amount of magnetite. Epidote and quartz formed simultaneously with magnetite. Fluid temperatures exceeded 500 C during the early to main stages. Fluid with very high salinity (50,75 wt% NaCl equiv.) was responsible for the formation of the magnetite ore. The oxygen isotope composition, together with the fluid inclusion data, suggests that magmatic fluid was significant for the formation of calc-silicate skarn minerals and magnetite. Low temperature (-230C) and low salinity (-10 % NaCl equiv.) hydrothermal fluids dominated by meteoric water were responsible for the late stage quartz and calcite formation. [source] | ||||||||||