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  • 1990-1994  (12)
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  • 1
    ISSN: 1438-1168
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Zusammenfassung In dieser Arbeit werden Sr, Nd und Pb Isotopendaten transitionaler Basalt-peralkalischer Rhyolithabfolgen und räumlich mit diesen assoziierter kalkalkalischer Rhyolithe der D' Entrecasteaux Inseln im östlichen Papua Neuguinea vorgestellt. Beide Abfolgen zeigen für konvergiernde Plattenränder typische geochemische Signaturen (z.B. hohe Zr/Nb, La/Nb und niedrige Ta/Yb Verhältnisse im Vergleich mit OIB). Die transitionale Basalt-peralkalische Rhyolithabfolge und die kalkalkalischen Rhyolithe zeigen eine geringe Variation in ihren206Pb/204Pb (18.522–18.661),207/204Pb (15.543–15.631) und208Pb/204Pb (38.31–38.63) Verhältnissen, die mit denen von Vulkaniten aus Tonga, Fiji und den pazifischen MOR-Basalten und Sedimenten übereinstimmen. Die transitionale Basalt-peralkalische Rhyolithabfolge zeigt weiters eine geringe Variationsbreite der143Nd/144Nd Verhältnisse (0.513053–0.512984), aber eine größere Streuung der87Sr/86Sr Verhältnisse (0.703989–0.70585). Letztere reflektiern die Unsicherheiten der Alterseinstufung der Proben mit sehr hohen87Rb/86Sr Verhältnissen und die Effekte des Sr-Austausches mit Meerwasser. Die87Sr/86Sr Verhältnisse kalkalkalischer Rhyolithe variieren im Vergleich dazu gerigfügiger (0.703864–0.704028). Isotopen und Spurenelementdaten sind mit der Interpretation, daß die kalkalkalischen Rhyolithe durch partielle Anatexis junger Inselbogen-Protkruste entstanden sind, kompatibel. Die mit ihnen vergesellschafteten basischen bis intermediären klakalkalischen Magmen entstammen einer abgereicherten Mantelquelle, die zuvor durch Subduktionsprozesse entlang des Trobriandgrabens modifiziert wurde. Die transitionale Basalt-peralkalische Rhyolithabfolge entstand durch extensive magmatische Differentiation eines transitionalen basaltischen Stammagmas in einer relativ seicht liegenden Magmenkammer. Das Stammagma wurde durch partielle Aufschmelzung entweder eines abgereicherten MORB-Mantels oder einer weniger stark abgereicherten OIBQuelle, die zuvor durch Subduktionsprozesse modifiziert wurde, gebildet. Die Hyund O1-normativen transitionalen Basaltmagmen wurden wahrscheinlich im Zuge der Ausdünnung von Lithosphäre unter etwas höheren Drucken gebildet als die Quarznormativen kalkalkaischen Magmen. Die enge räumliche und zeitliche Beziehung der transitionalen Basalt-peralkalischen Rhyolithabfolge mit kalkalkalischen Vulkaniten spiegelt die komplexen und dynamischen geotektonischen Vorgänge im östlichen Papua Neuguinea wieder. Der Wechsel von kalkalkalischem zu alkalischem Magmatismus könnte durch die Umstellung von Kompressions- auf Extensionstektonik, die mit der Verlagerung des westlich gelegenen Woodlark Spreadingzenrums in das östliche Papua Neugiunea in Beziehung gebracht wird, erklärt werden.
    Notes: Summary Sr, Nd and Pb isotope data are presented for a transitional basalt-peralkaline rhyolite suite, and spatially associated calc-alkaline rhyolites from the D'Entrecasteaux Islands, eastern Papua New Guinea. Both suites have a typical convergent margin geochemical signature (i.e. high Zr/Nb, La/Nb, and low Ta/Yb compared with OIB). The transitional basalt-peralkaline rhyolite suite and calc-alkaline rhyolites have a restricted range of206Pb/204Pb (18.522–18.661),207Pb/204Pb (15.543–15.631), and208Pb/204Pb (38.31–38.63) values which overlap the fields of volcanics from Tonga, Fiji, and Pacific MORB and sediments. The transitional basalt-peralkaline rhyolite suite also displays a restricted range of143Nd/144Nd values (0.513053–0.512984), but a much broader range of87Sr/86Sr (0.703989–0.70585) values. The latter reflects uncertainties in the ages of samples with very high87Rb/86Sr values and the effects of Sr exchange with seawater. The calc-alkaline rhyolites have consistently lower143Nd/144Nd values (0.512923—0.512867), and a more restricted range of87Sr/86Sr values (0.703864–0.704028) compared with the transitional basalt-peralkaline rhyolite suite. The isotopic and trace element data are consistent with the interpretation that the calc-alkaline rhyolites were produced by partial melting of a young arc protocrust, whereas associated calc-alkaline basic and intermediate magmas were derived from a depleted mantle source which previously had been modified by subduction along the Trobriand Trough. The transitional basalt-peralkaline rhyolite suite was produced by extensive magmatic differentiation of a parental transitional basalt magma in a relatively shallow magma chamber. The parent magma was produced by partial melting of either a depleted MORB-source mantle or a less-depleted OIB-type source which previously had been modified by subduction processes. The hy- and ol-normative transitional basalt magmas were probably generated in response to lithospheric thinning at somewhat higher pressures than qz-normative calc-alkaline magmas. The close spatial and temporal relationship between the transitional basalt-peralkaline rhyolite suite and the tale-alkaline volcanics reflects the complex and dynamic tectonic setting of eastern Papua and the D'Entrecasteaux Islands. In particular, the change from calc-alkaline to alkaline magmatism appears to have occurred following a change from compressional to extensional tectonics resulting from the westward propogation of the Woodlark spreading ridge into eastern Papua.
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  • 2
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Bacteria were enriched from soil samples with succinate as carbon source and racemic 2-phenylpropionitrile as sole source of nitrogen. One of the isolates, strain d3, converted (R,S)-2-phenylpropionitrile with high enantioselectivity to (S)-2-phenylpropionic acid. Strain d3 was identified as Agrobacterium tumefaciens. Resting cells hydrolysed 2-phenylpropionitrile via 2-phenylpropionamide to 2-phenylpropionic acid. Racemic 2-phenylpropionitrile as well as 2-phenylpropionamide were converted to (S)-2-phenylpropionic acid with an enantiometric excess above 96%. The nitrile hydratase and the amidase were both shown to convert preferentially the S enantiomer of their respective substrate. These two enzymes were induced in the presence of (R,S)-2-phenylpropionitrile but only in the absence of ammonia. In addition to 2-phenylpropionitrile strain d3 could utilize various aliphatic and aromatic nitriles as nitrogen sources. Resting cells of strain d3 also converted (R,S)-2-phenylbutyronitrile, ibuprofen nitrile, ketoprofen nitrile and α-aminophenylacetonitrile with high enantioselectivity. The nitrile- and amide-converting enzyme activities were also found in cell-free extracts.
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  • 3
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Bacteria were enriched from soil samples with succinate as carbon source and racemic 2-phenylpropionitrile as sole source of nitrogen. One of the isolates, strain d3, converted (R,S)-2-phenylpropionitrile with high enantioselectivity to (S)–2-phenylpropionic acid. Strain d3 was identified as Agrobacterium tumefaciens. Resting cells hydrolysed 2-phenylpropionitrile via 2-phenylpropionamide to 2-phenylpropionic acid. Racemic 2-phenylpropionitrile as well as 2-phenylpropionamide were converted to (S)-2-phenylpropionic acid with an enantiomeric excess above 96%. The nitrile hydratase and the amidase were both shown to convert preferentially the S enantiomer of their respective substrate. These two enzymes were induced in the presence of (R,S)-2-phenylpropionitrile but only in the absence of ammonia. In addition to 2-phenylpropionitrile strain d3 could utilize various aliphatic and aromatic nitriles as nitrogen sources. Resting cells of strain d3 also converted (R,S)-2-phenylbutyronitrile, ibuprofen nitrile, ketoprofen nitrile and α-aminophenylacetonitrile with high enantioselectivity. The nitrile- and amide-converting enzyme activities were also found in cell-free extracts.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 105 (1990), S. 585-601 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Major, trace-element, and Sr-, Nd-and Pbisotope data are presented for volcanics from 12 active or recently active volcanoes from the islands of Flores, Adonara, Lembata and Batu Tara in the eastern Sunda are. The volcanics vary in composition from low-K tholeiite, through medium-and high-K calcalkaline types to the K-rich leucite basanites of Batu Tara. From the tholeiites to the leucite basanites there are marked increases in the concentrations of LILE (K, Rb, Ba, Sr), LREE and La/Yb, and all the volcanics have high Ba/ Nb, La/Nb and Ba/La compared with mid-ocean ridge and intraplate eruptives. K/Cs values are generally lower than OIB values, and overlap those of other arc volcanics and northeast Indian Ocean sediments. The volcanics exhibit a broad range of 87Sr/86Sr (0.70468–0.70706), 143Nd/144Nd (0.512946–0.512447), and a moderate range in 206Pb/204Pb (18.825–19.143), 207Pb/ 204Pb (15.643–15.760) and 208Pb/204Pb (38.97–39.51). Trace-element and isotopic data suggest that the mantle beneath the eastern Sunda arc is a complex heterogeneous mixture of 3 or 4 major source components: MORB-source or depleted MORB-source, OIB-source and subducted Indian Ocean sediment. The low-K tholeiites were probably formed by relatively large degrees of melting of depleted MORB-source mantle, modified by subduction-related fluids, whereas the trace-element and isotopic characteristics of the K-rich volcanics suggest that they were derived from an OIB source which and been modified by a subduction-related melt component. The source components of the medium-to high-K calcalkaline rocks are more difficult to determine, and probably include mixtures of MORB-source or OIB-source, and melt/fluid derived from subducted oceanic sediment. Minor-and trace-element modelling calculations indicate substantial difficulties in producing the relatively low Ti-contents of arc volcanics by melting OIB-source mantle. Where OIB mantle is considered to be an important component of arc magmas it is suggested that the HFSE are buffered to relatively low concentration by a residual Ti-rich accessory phase.
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  • 5
    ISSN: 1432-1866
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Proterozoic silicic magmatic activity in the Tennant Creek area includes a suite of pre- to syn-orogenic granitoids (i.e. the Tennant Creek Granite and compositionally similar porphyries) predominantly intruded during the period 1870–1830 Ma, a group of silicic volcanics and volcaniclastics (Flynn Subgroup) erupted shortly after the main D1 deformation, and apparently anorogenic silicic intrusives represented by the Warrego Granite. Chemical and petrographic data indicate that the majority of the pre- to syn-orogenic granitoids and porphyries are I-type or infracrustal-derived, whereas the peraluminous muscovite-rich Warrego Granite has many characteristics of supracrustal-derived (S-type) granitoids. The Warrego Granite also appears to be moderately fractionated with relatively low Ba, Sr, Zr, K/Rb, and high Th, Nb, Be, Bi, Rb/Sr compared with the associated I-type granitoids, porphyries and volcanics. Fractionation of feldspar and minor zircon has also resulted in substantial relative enrichment in LREE together with a pronounced negative Eu anomaly in the Warrego Granite. Previous studies suggest that the Cu-Au-Bi mineralisation at Tennant Creek post-dates formation of the host ironstones, but the absolute timing is imprecisely known. Mass-balance calculations utilising background Au concentrations for potential source rocks suggest it is feasible for the Au in some of the deposits to have been leached by relatively high-temperature (250 to 300 °C) deep basinal brines, and deposited by reaction with the ironstones. However, the inferred hydrothermal leaching cells would need to have been very large unless the leaching process was very effective. An alternative preferred model is that the mineralising fluids were exsolved from incompatible element-enriched, fractionated granitic magma, mixed with ground water, and reacted with the ironstones to deposit the base and precious metals. On the basis of chemical similarity to other granitoids closely associated with mineralisation, the Warrego Granite seems the most likely source of the fluids. However, problematic constraints imposed by the apparent age of the mineralisation (1810 Ma), and an emplacement age (Rb-Sr) of 1670 Ma for the Warrego Granite indicate a need for additional geochronological studies.
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  • 6
    Publication Date: 1994-11-01
    Print ISSN: 0175-7598
    Electronic ISSN: 1432-0614
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Published by Springer
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  • 7
    Publication Date: 1994-10-01
    Print ISSN: 0175-7598
    Electronic ISSN: 1432-0614
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Published by Springer
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  • 8
    Publication Date: 1993-10-01
    Print ISSN: 1046-5928
    Electronic ISSN: 1096-0279
    Topics: Biology , Medicine
    Published by Elsevier
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  • 9
    Publication Date: 1990-10-01
    Print ISSN: 0010-7999
    Electronic ISSN: 1432-0967
    Topics: Geosciences
    Published by Springer
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  • 10
    Publication Date: 1992-05-01
    Print ISSN: 0361-0128
    Electronic ISSN: 1554-0774
    Topics: Geosciences
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