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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Environmental geology 29 (1997), S. 132-141 
    ISSN: 1432-0495
    Keywords: Key words Trace elements ; Indian rivers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract  Geochemical analyses of surface waters from rivers flowing through Orissa State, India, indicated that trace element concentrations were extremely variable and consistently higher than world river average. The Brahmani River was the most solute-rich river studied, followed by the Baitarani and Mahanadi Rivers. Although all three rivers drain similar geology, the Brahmani River catchment is heavily industrialized, and water samples collected upstream and downstream from industries indicated that anthropogenic activity directly influenced its chemical composition. Samples collected from several towns, in all three river systems, did not invariably show similar patterns, with various elements having higher dissolved concentrations upstream. Because the concentration of total solids increased downstream, this implied that some components of the sewage had effectively sequestered available elements from solution and converted them to particulate material. Although the impact of pollution is clearly recognizable in water samples collected in proximity to the anthropogenic source, there are only slight elemental accumulations in the lower reaches of the Mahanadi River, with no accumulation in the Brahmani River. Apparently for these large rivers, discharged effluent becomes rapidly diluted, while complexation and sedimentation further removes trace elements from the water column. However, in the less voluminous Baitarani River, elementar enrichment near the river's mouth suggests that in this secondary river, where dilution effects are less, the concerns over regional water quality may be more prevalent.
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford UK : Blackwell Science Ltd
    Sedimentology 45 (1998), S. 0 
    ISSN: 1365-3091
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: Tectonically isolated blocks of carbonate rocks present within the anhydritic Haselgebirge mélange of the Northern Calcareous Alps record a complex history of deformation and associated deep-burial diagenetic to very low-grade metamorphic reactions. Fluids were hot (up to ≈ 250 °C) and reducing brines charged with carbon dioxide. Individual carbonate outcrops within the mélange record different regimes of brine–rock reactions, ranging from pervasive dolomite recrystallization to dedolomitization. Early diagenetic features in these carbonates were almost entirely obliterated. Matrix dolomite alteration was related to thermochemical sulphate reduction (TSR) recognized by the replacement of anhydrite by calcite + pyrite ± native sulphur. Pyrite associated with TSR is coarsely crystalline and characterized by a small sulphur isotope fractionation relative to the precursor Permian anhydrite. Carbonates associated with TSR show low Fe/Mn ratios reflecting rapid reaction of ferrous iron during sulphide precipitation. As a result, TSR-related dolomite and calcite typically show bright Mn(II)-activated cathodoluminescence in contrast to the dull cathodoluminescence of many (ferroan) carbonate cements in other deep-burial settings. In addition to carbonates and sulphides, silicates formed closely related to TSR, including quartz, K-feldspar, albite and K-mica. 40Ar/39Ar analysis of authigenic K-feldspar yielded mostly disturbed step-heating spectra which suggest variable cooling through the argon retention interval for microcline during the Late Jurassic. This timing coincides with the recently recognized subduction and closure of the Meliata-Hallstatt ocean to the south of the Northern Calcareous Alps and strongly suggests that the observed deep-burial fluid–rock reactions were related to Jurassic deformation and mélange formation of these Permian evaporites.
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  • 3
    ISSN: 1365-3091
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: The Middle Muschelkalk (Middle Triassic) of the Catalan Coastal Range (north-east Spain) comprises sandstone, mudstone, anhydrite and minor carbonate layers. Interbedded sandstones and mudstones which are dominant in the north-eastern parts of the basin are terminal alluvial fan deposits. South-westward in the basin, the rocks become dominated by interbedded evaporites and mudstones deposited in sabkha/mudflat environments. The diagenetic and pore water evolution patterns of the Middle Muschelkalk suggest a strong facies control. During eodiagenesis, formation of microdolomite, anhydrite, baryte, magnesite, K-feldspar and mixed-layer chlorite/smectite was favoured within and adjacent to the sabkha/mudflat facies, whereas calcite, haematite, mixed-layer illite/smectite and quartz formed mainly in the alluvial facies. Low δ18OSMOW values for microdolomite (+23.7 to +28.4%) and K-feldspar overgrowths (+17.3 to +17.7%) suggest either low-temperature, isotopic disequilibrium or precipitation from low-18O porewaters. Low-18O waters might have developed, at least in part, during low-temperature alteration of volcanic rock fragments. During mesodiagenesis, precipitation of quartz overgrowths and coarse dolomite occurred in the alluvial sandstones, whereas recrystallization of microdolomite was dominant in the sabkha/mudflat facies. The isotopic compositions of these mesogenetic phases reflect increasing temperature during burial. Upon uplift and erosion, telogenetic calcite and trace haematite precipitated in fractures and replaced dolomite. The isotopic composition of the calcite (δ18OSMOW=+21.5 to +25.6%o; δ13C= 7.7 to - 5.6%o) and presence of haematite indicate infiltration of meteoric waters.
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  • 4
    ISSN: 1365-3091
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: Early diagenesis of the Upper Cretaceous (late Coniacian to early Santonian) Marshybank Formation was controlled by depositional environment (composition of depositional water, Fe and organic content of the sediment, sedimentation rate, proximity to the shoreline) and influx of meteoric water related to relative sea-level fall.Five depositional environments, each characterized by a distinct early diagenetic mineral assemblage, have been recognized. Offshore shelf sediments that were deposited in a dysaerobic environment are characterized by abundant framboidal pyrite and rare septarian concretions, composed of ‘early’ calcite and siderite. Intense sulphate reduction, promoted by the dysaerobic depositional water, was the primary influence on early diagenesis. Offshore shelf sediments deposited under aerobic conditions are characterized by abundant concretions, composed of two generations of siderite (S1 and S2). In this environment, methanogenesis, rather than sulphate reduction, was more important. Early diagenesis of the inner shelf sands was generally limited. However, in sands deposited proximal to the shoreline, mixing of marine and meteoric waters promoted crystallization of Fe-rich chlorite and siderite. The shoreface was characterized by dissolution of detrital minerals in the upper portion, and precipitation of kaolinite or illite/smectite in the lower portion. In the coastal plain environment, brackish water and early reducing conditions resulted in formation of abundant euhedral pyrite. Ankerite, rather than siderite, is the typical early diagenetic carbonate.The δ18O values of the earliest cements (i.e. ‘early’ calcite, siderite S1, inner shelf siderite) indicate crystallization from a low-18O, marine-derived porewater. Assuming crystallization at 25°C, a δ18O value of about −7‰ (SMOW) can be estimated for the seaway during Marshybank Formation time. Similar calculations for the overlying Dowling Member (Puskwaskau Formation) suggest that the δ18O value of the seaway increased to about −4% (SMOW), consistent with its transgressive nature. Very low δ18O values are exhibited by siderite S2. These results indicate crystallization during intermediate diagenesis (≥60°C) from meteoric water (≥− 15‰ SMOW) that entered the Marshybank Formation during sea-level lowstand.
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  • 5
    Publication Date: 2011-10-24
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 6
    Publication Date: 2013-02-01
    Description: Three types of subvertical leucogranites and pegmatites populate the Red Cross Lake pegmatite field, located in the Red Cross Lake greenstone belt of the Sachigo Subprovince, in the northwestern part of the Archean Superior Province of the Canadian Shield. The greenstone belt is situated in the northern margin of the Oxford–Stull domain of the North Caribou terrane, in tectonic contact with the Hudson Bay terrane. The tholeiitic greenstone belt, flanked by plutonic masses of tonalitic gneiss to the north and tonalite–granodiorite gneiss to the south, consists of a bimodal assemblage of metabasalt + subvolcanic metagabbro and felsic lapilli tuff of andesitic to rhyolitic compositions, mafic mylonite with a mylonitized granitoid, and volcaniclastic metagreywacke. Regional context and petrochemical features of the south-flanking tonalitic-granodioritic masses and of the greenstone-belt lithologies indicate a largely juvenile, deep-oceanic origin. To the north, the isotopic signatures of tonalitic-granodioritic masses indicate an older continental association. The leucogranites and pegmatites and related intrusions were subvertically emplaced into, or alongside, the predominantly mylonitized metavolcanic rocks of the WNW–ESE-trending North Kenyon Shear Zone. Some of the leucogranites are geochemically rather primitive, but they grade into more evolved pegmatite bodies and ultimately into extremely fractionated lepidolite-subtype pegmatites. Investigation of the origin of the rare-element enrichment in these pegmatites, within the limits of our reconnaissance sampling, did not show above-average enrichment of rare lithophile elements in any of the main regional map units.
    Print ISSN: 0008-4476
    Topics: Geosciences
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  • 7
    Publication Date: 2013-02-01
    Description: Spatial relations and bulk chemical compositions of three bodies of multiphase leucogranites and two categories of granitic pegmatites in the Archean Red Cross Lake greenstone belt, Sachigo Subprovince of the Superior Province in the Canadian Shield, indicate a comagmatic origin and an enormous range of fractionation. The leucogranite + pegmatite assemblages, probably emplaced at ~2.65 Ma, represent an upward fingering-out system presumably rooted in a deeper-seated granitic parent, which was derived by anatexis of felsic lithologies of the greenstone belt, with possible contribution from granitoid components of the flanking plutonic terranes. The leucogranitic melts so derived underwent extensive fractionation, culminating in the lepidolite pegmatites that solidified within the relatively low-P – high-T stability field of petalite. The most primitive fine-grained NGR leucogranite shows a K/Rb of 303. In contrast, the most evolved LPG lepidolite-type pegmatites [with albite 〉〉 K-feldspar, K-, Rb- and Cs-dominant lepidolite, spodumene + quartz after petalite, elbaite, beryl, pollucite, amblygonite, and (Ta,Sn)- oxide minerals] average K/Rb 1.8, and Cs 4199, Be 236, Ga 161, Nb 14, and Ta 349 ppm. Crystal–liquid and gravity-assisted liquid–liquid fractionation and differential solubilities of HFSE in the melts could have cooperated with selective complexing of elements and mass-controlled diffusion rates to attain the extreme enrichment and fractionation observed at the scale of pegmatite dikes down to local crystal-matrix levels. The bulk chemical composition of the dikes was not affected by mylonitization. The oxygen-isotope signature of the pegmatites also suggests relatively dry conditions during shearing, with very limited exchange with the host rocks. In contrast, the Rb–Sr isotopes are extensively disturbed in both the leucogranites and LPG dikes.
    Print ISSN: 0008-4476
    Topics: Geosciences
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  • 8
    Publication Date: 2014-01-11
    Description: In situ thermal recovery methods such as cyclic steam stimulation (CSS) are required to extract highly viscous bitumen from the Clearwater Formation oil sands of Alberta, Canada. The injection of hot fluids during CSS has altered the mineralogy of the sands, resulting in the loss of some minerals ( e.g. disseminated siderite, volcanic glass) and precipitation of others ( e.g. zeolites and abundant hydroxy-interlayered smectite). The high temperatures and high water–rock ratios associated with CSS might also alter the oxygen and hydrogen isotopic compositions of pre-existing clay minerals even in the absence of mineralogical changes. The present study exploits this fact to track the movement of injected hot fluids during CSS. Berthierine, a common diagenetic clay mineral in the Clearwater sands, survived CSS but acquired substantially lower 18 O and 2 H values in cores located ≤10 m from the injection well. In contrast, the oxygen and hydrogen isotopic compositions of berthierine in cores located further from the injection well were generally unaffected, except at the depth of steam injection where horizontal fractures facilitate greater lateral penetration of hot fluids. Smectitic clays in near-injector cores also acquired lower 18 O values during CSS, but a systematic shift in 2 H values was not observed. While hydrogen-isotope exchange undoubtedly occurred, the particular combination of temperature and H isotopic composition of the injected fluid used during CSS appears to have yielded post-steam 2 H values that are indistinguishable from pre-steam values. Only samples from near-injector core G-OB3 that contain hydroxy-interlayered smectite have lower 2 H values as a result of CSS.
    Print ISSN: 0009-8604
    Electronic ISSN: 1552-8367
    Topics: Geosciences
    Published by Clay Minerals Society
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  • 9
    Publication Date: 2014-12-31
    Description: Existing radiocarbon (14C) dates on American mastodon (Mammut americanum) fossils from eastern Beringia (Alaska and Yukon) have been interpreted as evidence they inhabited the Arctic and Subarctic during Pleistocene full-glacial times (∼18,000 14C years B.P.). However, this chronology is inconsistent with inferred habitat preferences of mastodons and correlative paleoecological evidence....
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 10
    Publication Date: 2013-07-24
    Description: Dioctahedral clays from an active continental geothermal system have been studied to assess their usefulness as proxies of paleo-hydrological and thermal conditions in the subsurface. Drill cuttings from Well WK244 in the Te Mihi area of the Wairakei Geothermal Field, New Zealand, were analyzed to determine the mineralogical, morphological, and isotopic characteristics of hydrothermal clays in these samples. Mixed-layer illite-dioctahedral smectite (I-S) and R0 chlorite-trioctahedral smectite are the main clay minerals, with I-S clays varying downward from R1 to R3 ordering and 50 to 〉90% illite over 160 m. The proportion of illite in I-S correlates positively with downhole temperature (r = 0.98) and I-S morphology changes from high aspect ratio ribbons, laths, and hairy fibers to pseudo-hexagonal plates with depth. Swelling clay percentages determined using the methylene blue method show a strong positive correlation with %S in I-S (r = 0.91), validating use of methylene blue as a rapid field tool for characterizing the smectite to illite transition in this active geothermal environment. The oxygen isotopic composition of I-S ( 18 O I-S ) decreases systematically with depth, and mostly reflects a progressive increase in subsurface temperature during clay formation. Estimates of water/rock ratios calculated using 18 O I-S values display stratigraphic variability that corresponds to variations in permeability. Oxygen isotopic measurements of I-S are a useful tool for understanding reservoir and permeability evolution in such geothermal systems and their related fossil analogs.
    Print ISSN: 0009-8604
    Electronic ISSN: 1552-8367
    Topics: Geosciences
    Published by Clay Minerals Society
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