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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 450 (2007), S. 1169-1170 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] It was almost 40 years ago that we found out what the Moon is made of: lunar samples collected during the Apollo missions turned out to consist of rocky material similar in composition to that found on Earth. We also think we know that the Moon formed from the accretion of molten and vaporized ...
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Crustal contamination of basalts located in the western United States has been generally under-emphasized, and much of their isotopic variation has been ascribed to multiple and heterogeneous mantle sources. Basalts of the Miocene Columbia River Basalt Group in the Pacific Northwest have passed through crust ranging from Precambrian to Tertiary in age. These flows are voluminous, homogenous, and underwent rapid effusion, all of which are disadvantages for crustal contamination while en route to the surface. The Picture Gorge Basalt of the Columbia River Basalt Group erupted through Paleozoic and Mesozoic oceanic accreted terranes in central Oregon, and earlier studies on these basalts provided no isotopic evidence for crustal contamination. New Sr, Nd, Pb, and O isotopic data presented here indicate that the isotopic variation of the Picture Gorge Basalt is very small, 87Sr/86Sr=0.70307–0.70371, ɛNd=+7.7-+4.8, δ18O=+5.6±6.1, and 206Pb/204Pb=18.80–18.91. Evaluation of the Picture Gorge compositional variation supports a model where two isotopic components contributed to Picture Gorge Basalt genesis. The first component (C1) is reflected by low 87Sr/86Sr, high ɛNd, and nonradiogenic Pb isotopic compositions. Basalts with C1 isotopic compositions have large MgO, Ni, and Cr contents and mantle-like δ18O=+5.6. C1 basalts have enrichments in Ba coupled with depletions in Nb and Ta. These characteristics are best explained by derivation from a depleted mantle source which has undergone a recent enrichment by fluids coming from a subducted slab. This C1 mantle component is prevalent throughout the Pacific Northwest. The second isotopic component has higher 87Sr/ 86Sr and δ18O, lower ɛNd, and more radiogenic Pb isotopic compositions than C1. There is a correlation in the Picture Gorge data of Sr, Nd, and Pb isotopes with differentiation indicators such as decreasing Mg#, and increasing K2O/TiO2, Ba, Ba/Zr, Rb/Sr, La/Sm, and La/Yb. Phase equilibrium and mineralogical constraints indicate that these compositional characteristics were inherited in the Picture Gorge magmas at crustal pressures, and thus the second isotopic component is most likely crustal in origin. Mixing and open-system calculations can produce the isotopic composition of the most evolved Picture Gorge flows from the most primitive compositions by 8 to 21% contamination of isotopic compositions similar to accreted terrane crust found in the Pacific Northwest. Therefore, in spite of the disadvantages for crustal contamination and their narrow range in isotopic compositions, the process controlling isotopic variation within the Picture Gorge Basalt is primarily crustal contamination. We suggest that comprehensive analyses for basaltic suites and careful consideration of these data must be made to test for crustal contamination, before variation resulting from mantle heterogeneity can be assessed.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 109 (1992), S. 275-294 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The peraluminous Drammen batholith (650 km2) is the largest granite complex within the mainly alkaline province of the Permo-Carboniferous Oslo Rift, and peraluminous to metaluminous granites are also present in the southern part of the otherwise alkaline Finnemarka complex (125 km2). The emplacement of the Drammen granite, and probably most of the other biotite granite complexes, predate the alkaline syenites and granites. The eight separate petrographic types of the Drammen batholith range in SiO2 from 70 to 79 wt.% and have experienced variable amounts of fractionation of feldspars, biotite, zircon, apatite, titanite and Fe−Ti-oxides. The initial Sr, Nd and Pb isotopic ratios and a decoupling between the variations in the SiO2 content and the aluminum saturation index [ASI=Al2O3/(CaO+Na2O +K2O)] show that the various intrusive phases are not strictly comagmatic. The εNd values of the southern part of Finnemarka (+3.5 to +4) and the northern part of the Drammen granite (+1 to +1.5) are high and indicate insignificant (for Finnemarka) to minor Precambrian crustal or enriched mantle contributions. The very low εSr values of all of these samples (−1 to −12, outside the main Oslo Rift magmatic array), point to a time integrated Rb-depleted crustal contaminant or an EM1 mantle component. The earliest extruded alkali basalts along the southwestern margin of the Oslo Rift are the only other samples within this low εSr area, but their isotopic signature may also be linked to a mantle enrichment event (involving an EM1 component), e.g. associated with the Fen carbonatite magmatism 540 Ma ago. For a given 206Pb/204Pb, the 208Pb/204Pb ratios of the Drammen and Finnemarka batholiths are distinctly lower than those of the Skien alkaline volcanics and all other magmatic Oslo Rift rocks. This may indicate that the lithosphere of the central part of the rift had a time integrated Th-depletion. The samples from the southern part of the Drammen batholith, characterized by the presence of abundant miarolitic cavities, have εNd near 0 (−0.7 to +0.4) but strongly elevated εSr of +35 to +67. The combined Pb isotopic ratios of all the samples analyzed indicate that the Precambrian crustal anatectic contribution is in the form of time integrated Th-and U-depleted lower crust, and the high +Sr of the sourthern part of the Drammen granite results from shallow level wallrock assimilation or magma-fluid interactions. The remarkably low contribution of old crustal components to the Finnemarka and the northernmost Drammen batholiths may result from extensive late Precambrian intracustal differentiation in southwestern Scandinavia, leading to widespread upper crustal granites (≈ 900 Ma) and a correspondingly dense and refractory lower crust, in particular in a zone intersecting the central part of the rift. Liquidus phase relations and mass-balance constrainst permit derivation of the granites from mildly alkaline to tholeiitic melts by extensive crystal fractionation of clinopyroxene-and amphibole-rich assemblages. It is equally possible to form the granitic magmas by partial melting of Permian gabbros of similar composition. Either scenario is consistent with the isotopic constrainst and with the presence of dense cumulates and/or residues in the lower crust. The lack of igneous rocks of intermediate composition associated with the Drammen and Finnemarka batholiths point to an efficient upper crustal density filtering. Considerable amounts of heat would be accumulated in this region if differentiated, intermediate melts could not escape to shallower levels. Successive magma injections would therefore easily result in partial melting of already solidified mafic to intermediate melts and cumulates, and it is suggested that the peraluminous granites formed mainly by water-undersaturated anatexis of mafic material.
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  • 4
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    PANGAEA
    In:  Supplement to: Brandon, Alan D; Snow, Jonathan E; Walker, Richard J; Morgan, John W; Mock, Timothy D (2000): 190Pt-186Os and 187Re-187Os systematics of abyssal peridotites. Earth and Planetary Science Letters, 177(3-4), 319-335, https://doi.org/10.1016/S0012-821X(00)00044-3
    Publication Date: 2024-01-09
    Description: Abyssal peridotites are normally thought to be residues of melting of the mid-ocean ridge basalt (MORB) source and are presumably a record of processes affecting the upper mantle. Samples from a single section of abyssal peridotite from the Kane Transform area in the Atlantic Ocean were examined for 190Pt-186Os and 187Re-187Os systematics. They have uniform 186Os/188Os ratios with a mean of 0.1198353 +/- 7, identical to the mean of 0.1198340 +/-12 for Os-Ir alloys and chromitites believed to be representative of the upper mantle. While the Pt/Os ratios of the upper mantle may be affected locally by magmatic processes, these data show that the Pt/Os ratio for the bulk upper mantle has not deviated by more than about +/- 30% from a chondritic Pt/Os ratio over 4.5 billion years. These observations are consistent with the addition of a chondritic late veneer after core separation as the primary control on the highly siderophile element budget of the terrestrial upper mantle. The 187Os/188Os of the samples range from 0.12267 to 0.12760 and correlate well with Pt and Pt/Os, but not Re/Os. These relationships may be explained by variable amounts of partial melting with changing D(Re), reflecting in part garnet in the residue, with a model-dependent melting age between about 600 and 1700 Ma. A model where the correlation between Pt/Os and 187Os/188Os results from multiple ancient melting events, in mantle peridotites that were later juxtaposed by convection, is also consistent with these data. This melting event or events are evidently unrelated to recent melting under mid-ocean ridges, because recent melting would have disturbed the relationship between Pt/Os and 187Os/188Os. Instead, this section of abyssal peridotite may be a block of refractory mantle that remained isolated from the convecting portions of the upper mantle for 600 Ma to 〉1 Ga. Alternatively, Pt and Os may have been sequestered during more recent melting and possibly melt/rock reaction processes, thereby preserving an ancient melting history. If representative of other abyssal peridotites, then the rocks from this suite with subchondritic 187Os/188Os are not simple residues of recent MORB source melting at ridges, but instead have a more complex history. This suite of variably depleted samples projects to an undepleted present-day Pt/Os of about 2.2 and 187Os/188Os of about 0.128-0.129, consistent with estimates for the primitive upper mantle.
    Keywords: 153-920B; 153-920D; DRILL; Drilling/drill rig; Joides Resolution; Leg153; Ocean Drilling Program; ODP; South Atlantic Ocean
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 5
    Publication Date: 2024-01-09
    Keywords: 153-920B; 153-920D; Calculated from weight loss after ignition at 550 °C; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Event label; Isotope ratio mass spectrometry; Joides Resolution; Leg153; Mass spectrometer VG Sector 54; Multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS); Ocean Drilling Program; ODP; ORDINAL NUMBER; Osmium; Osmium-184/Osmium-188, error; Osmium-184/Osmium-188 ratio; Osmium-186/Osmium-188, error; Osmium-186/Osmium-188 ratio; Osmium-187/Osmium-188, error; Osmium-187/Osmium-188 ratio; Platinum; Platinum-187/Osmium-188 ratio; Rhenium; Rhenium-187/Osmium-188 ratio; Sample code/label; Sample code/label 2; South Atlantic Ocean
    Type: Dataset
    Format: text/tab-separated-values, 190 data points
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  • 6
    Publication Date: 2024-01-09
    Keywords: 153-920B; 153-920D; Aluminium oxide; Calcium oxide; Chromium; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Event label; Iron oxide, FeO; Joides Resolution; Leg153; Loss on ignition; Magnesium number; Magnesium oxide; Manganese oxide; Nickel; Ocean Drilling Program; ODP; Phosphorus pentoxide; Potassium oxide; Sample code/label; Sample code/label 2; Silicon dioxide; Sodium oxide; South Atlantic Ocean; Strontium; Titanium dioxide; X-ray fluorescence (XRF)
    Type: Dataset
    Format: text/tab-separated-values, 102 data points
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  • 7
    Publication Date: 2024-01-09
    Description: The compatibility of vanadium (V) during mantle melting is a function of oxygen fugacity (fO2): at high fO2's, V becomes more incompatible. The prospects and limitations of using the V content of peridotites as a proxy for paleo-fO2 at the time of melt extraction were investigated here by assessing the uncertainties in V measurements and the sensitivity of V as a function of degree of melt extracted and fO2. V-MgO and V-Al2O3 systematics were found to be sensitive to fO2 variations, but consideration of the uncertainties in measurements and model parameters indicates that V is sensitive only to relative fO2 differences greater than ~2 log units. Post-Archean oceanic mantle peridotites, as represented by abyssal peridotites and obducted massif peridotites, have V-MgO and -Al2O3 systematics that can be modeled by 1.5 GPa melting between FMQ - 3 and FMQ - 1. This is consistent with fO2's of the mantle source for mid-ocean ridge basalts (MORBs) as determined by the Fe3+ activity of peridotitic minerals and basaltic glasses. Some arc-related peridotites have slightly lower V for a given degree of melting than oceanic mantle peridotites, and can be modeled by 1.5 GPa melting at fO2's as high as FMQ. However, the majority of arc-related peridotites have V-MgO systematics overlapping that of oceanic mantle peridotites, suggesting that although some arc mantle may melt under slightly oxidizing conditions, most arc mantle does not. The fact that thermobarometrically determined fO2's in arc peridotites and lavas can be significantly higher than that inferred from V systematics, suggests that V retains a record of the fO2 during partial melting, whereas the activity of Fe3+ in arc peridotitic minerals and lavas reflect subsequent metasomatic overprints and magmatic differentiation/emplacement processes, respectively. Peridotites associated with middle to late Archean cratonic mantle are characterized by highly variable V-MgO systematics. Tanzanian cratonic peridotites have V systematics indistinguishable from post-Archean oceanic mantle and can be modeled by 3 GPa partial melting at ~FMQ - 3. In contrast, many South African and Siberian cratonic peridotites have much lower V contents for a given degree of melting, suggesting at first glance that partial melting occurred at high fO2's. More likely, however, their unusually low V contents for a given degree of melting may be artifacts of excess orthopyroxene, a feature that pervades many South African and Siberian peridotites but not the Tanzanian peridotites. This is indicated by the fact that the V contents of South African and Siberian peridotites are correlated with increases in SiO2 content, generating data arrays that cannot be modeled by partial melting but can instead be generated by the addition of orthopyroxene through processes unrelated to primary melt depletion. Correction for orthopyroxene addition suggests that the South African and Siberian peridotites have V-MgO systematics similar to those of Tanzanian peridotites. Thus, if the Tanzanian peridotites represent the original partial melting residues, and if the South African and Siberian peridotites have been modified by orthopyroxene addition, then there is no indication that Archean cratonic mantle formed under fO2's significantly greater than that of modern oceanic mantle. Instead, the fO2's inferred from the V systematics in these three cratonic peridotite suites are within range of modern oceanic mantle. This also suggests that the transition from a highly reducing mantle in equilibrium with a metallic core to the present oxidized state must have occurred by late Archean times.
    Keywords: 153-920; Aluminium oxide; Calcium oxide; Calculated; COMPCORE; Composite Core; DSDP/ODP/IODP sample designation; Iron oxide, FeO; Joides Resolution; Leg153; Magnesium oxide; Manganese oxide; Ocean Drilling Program; ODP; Phosphorus pentoxide; Potassium oxide; Sample code/label; Silicon dioxide; Sodium oxide; South Atlantic Ocean; Sum; Titanium dioxide; Vanadium; X-ray fluorescence (XRF)
    Type: Dataset
    Format: text/tab-separated-values, 78 data points
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  • 8
  • 9
  • 10
    Publication Date: 2020-09-01
    Print ISSN: 0016-7037
    Electronic ISSN: 1872-9533
    Topics: Chemistry and Pharmacology , Geosciences
    Published by Elsevier
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