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  • 1
    ISSN: 1365-3121
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: Clinopyroxene/melt pairs in strongly potassic silicate and carbonatite melts exhibit unusually high U/Th partitioning ratios of ˜ 3 and ˜ 2, respectively. These values are much higher than those found for aluminous clinopyroxenes in peridotite, and have the potential to cause significant (230Th)/(238U) isotope enrichment in volcanics. The potassic silicate (lamproite) and carbonatite melts correspond closely to the main agents of mantle metasomatism, indicating that clinopyroxene in metasomatized regions of the mantle may greatly affect U/Th disequilibria. Recycling of alkali pyroxenite veins in the oceanic lithosphere formed by solidification of melt in the extremities of the MORB melting region presents an alternative to eclogite recycling in MORB and OIB genesis.
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  • 2
    ISSN: 1438-1168
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Zusammenfassung Sm-Nd- und Rb-Sr-Isotope wurden in einer Abfolge von K-reichen OlivinTrachybasalten im Manning Massiv in den nördlichen Prince Charles Mountains, Ost-Antarktis, untersucht. Proben wurden systematisch von mehreren sich überlagernden Lavaströmen genommen, die Mächtigkeiten von 3,5 bis 6,5 m erreichen und dem Lambert-Amery Rift zugeordnet werden. Nd-Sr Isotopenzusammensetzung der Vulkanite sind ähnlich wie in Iherzolithischen Mantelxenolithen aus alkalischen Ultramafiten der Jetty Halbinsel. Allerdings deuten die Spurenelementgehalte sowie die Spurenelementverteilungen auf die Anwesenheit von Apatit, Amphibol, Ilmenit und Perowskit in der Quellenregionhin. Nd-Sr Isotope der Trachybasalte (143Nd/144Nd= 0.512026–0.512269;87Sr/86Sr = 0.707765–0.708046) weisen auf eine angereicherte Mantelzusammensetzung hin. Für die hier gefundenen Werte wird ein Mischungsmodell zwischen einem Peridotit-Nebengestein ähnlich wie in den Jetty Halbinsel Xenolithen und einer Schmelze vorgeschlagen, die aus ultramafischen Gängen innerhalb der Lithosphäre stammte. Die Kombination aus Isochronenalter und Modellalter der Vulkanite und der Xenolithe zeigt, daß nach der Bildung vor 1.2 Ga die Lithosphäre zwei Anreicherungsereignisse vor 0.9-1.0 Ga und 0.6 Ga erfahren hatte. Trotz der hohen Variation der143Nd/144Nd Verhältnisse ergeben sich für die unteren Lavaströme höhere Werte, während die oberen Bereiche an143Nd verarmt sind. Dies kann auf eine stetige Abnahme des Gang/Peridotit Verhältnisses von 35% auf 10% zurückgeführt werden, das auf eine fortschreitende Aufheizung der Quellenregion hinweist. Die Variation im143Nd/144Nd System wird aber nicht von einem Anstieg des87Sr/86Sr Verhältnisses begleitet, was mit ähnlichen Werten sowohl für die Gänge als auch für den angrenzenden Peridotit erklärt werden kann: das Nebengestein bestand aus einem angereicherten Peridotit, während die Gänge hauptsächlich aus Klinopyroxen und Amphibol zusammengesetzt waren. SEE-reiche Phasen wie Apatit und Perowskit kamen in so geringen Mengen vor, daß die Gesamtzusammensetzung der Gänge hohe Sr/Nd-Verhältnisse hatte. Rb-Sr Altersbestimmungen an Gesamtgesteinen der Manning Massiv-Vulkanite ergeben eine scheinbare Isochrone von 40±1.2 Ma (ISr = 0.70762), obwohl diese Altersinformation vermutlich durch die Mischungsprozesse während des partiellen Schmelzens verfälscht ist.
    Notes: Summary Rb-Sr and Sm-Nd isotopic investigations have been carried out on samples forming a sequence from the bottom to the top of a suite of K-rich olivine trachybasalts from the Manning Massif in the northern Prince Charles Mountains, East Antarctica. Several separate flows, each 3.5-6.5 m thick, occur as individual small outcrops and are related to the Lambert-Amery rift. Nd-Sr isotopic features of the volcanics are similar to those for lherzolite xenoliths from the Mesozoic alkaline ultramafic rocks of the adjacent Jetty Peninsula area, but the trace element abundances and patterns are consistent with the occurrence of minor phases such as apatite, amphibole, ilmenite and perovskite in the source region. According to Nd-Sr isotopic characteristics (143Nd/144Nd = 0.512026-0.512269;87Sr/86Sr = 0.707765-0.708046), the trachybasalts were generated from an enriched mantle source. These features are suggested here to result from isotopic mixing between peridotite wall-rocks similar to the Jetty Peninsula xenolith samples and melts derived from ultramafic veins in the lithosphere. A synthesis from isochron and model ages on volcanics and xenoliths indicates formation of the lithosphere at about 1.2 Ga, followed by two episodes of subsequent enrichment at 0.91.0 Ga and ca. 0.6 Ga. The143Nd/144Nd values for the volcanics show a wide range, but are more enriched for the bottom part of the suite, becoming more depleted towards the top. This may be explained by a steadily decreasing vein/wall-rock ratio from 35% to 10% due to progressive heating of the source region. This variation in ENd is not accompanied by a corresponding increase in87Sr/86Sr, which constrains both vein and wall-rock characteristics quite closely: the wall-rock was an enriched peridotite, whereas the vein assemblage comprised dominantly clinopyroxene and amphibole with a lesser, but essential, amount of phlogopite. REE-rich accessory phases such as apatite and perovskite were present in the vein, but were rare, so that the vein as a whole had high Sr/Nd. Rb-Sr age determination on Manning Massif bulk rocks gives an apparent isochron age of 40±1.2 Ma (ISr = 0.70762), although the age is probably falsified by the mixing processes during melting.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Mineralogy and petrology 34 (1985), S. 217-238 
    ISSN: 1438-1168
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Zusammenfassung Die Olivin-Leuzitite vom Gaussberg Vulkan, Antarktis, gehören zu den primären Gliedern der Lamproit-Gruppe der ultra-kalireichen Gesteine. Sie sind reich an Glas, weisen Mg-Werte um 70 auf, und führen Spinell-Lherzolith Xenolithe. Die Liquidus-Phasengleichgewichte bei Atmosphärendruck unter kontrollierten Sauerstoff-Partialdruckbedingungen wurden untersucht. Um Chromit als Liquidusphase zu stabilisieren, war es erforderlich, Cr2O3 zu den experimentellen Zusammensetzungen hinzuzufügen, obwohl Chromspinell als Einschluß in Olivin in den Ausgangsgesteinen auftritt; dies deutet eine Spinell-Franktionierung an. Die Resultate zeigten, daß diefO2-Bedingungen bei der Kristallisation durch das Fe3+-Verhältnis (100 Fe3+/(Fe3++Fe2+)) im Spinell, durch den Fe3+-Gehalt im Leuzit, und durch den Mg-Wert (100 mg/(Mg+Fe2+)) im Olivin charakterisiert sind. Die Liquidusphasen der Gaussberg Gesteine kristallisierten beifO2-Bedingungen etwas unterhalb NNO. Die Anwendung der Resultate auf andere Lamproite zeigt, daß diese unter Sauerstoff-Partialdruckbedingungen kristallisierten, die von oberhalb NNO (Leucite Hills) bis etwa MW (West Kimberley und die Spanish Fortunites) variierten. Der Gaussberg Olivin-Leuzitit enthält Leuzitkristalle mit deutlicher Zonierung; die Kernbereiche sind arm an dreiwertigem Eisen, während die Randzonen deutlich an Fe3+ angereichert sind. Dies weist auf eine Oxidation des Magmas während der Platznahme hin. Das Fe3+-Verhältnis der Spinelle ist sehr empfindlich gegenüber Änderungen des Sauerstoff-Partialdruckes; da einige lamproitische Magmen Diamanten führen, könnte sich dieses als ein sinnvoller Indikator für eine mögliche Diamantführung erweisen. Die Überlebensfähigkeit von Diamanten in lamproitischen Gesteinen wird sehr stark abhängig sein vonfO2: Magmen, die die Oberfläche unterfO2-Bedingungen entsprechend NNO oder darüber erreichten, werden keine Diamanten mehr erhalten.
    Notes: Summary Olivine leucitites from the Gaussberg volcano, Antarctica are primitive members of the lamproite group of ultrapotassic rocks. They are glass rich, have an Mg number of around 70, and carry spinel lherzolite xenoliths. Liquidus phase fields and compositions were studied experimentally at atmospheric pressure with controlled oxygen fugacities. Chrome-spinels occur as inclusions in olivines in the natural rock, but it was necessary to add Cr2O3 to the experiments to stabilize spinels at the liquidus, indicating that some fractionation of spinel has almost certainly occurred. Experimental results show thatfO2 conditions of crystallization can be characterized by ferric value (100 Fe3+/(Fe3++Fe2+)) of spinel, ferric iron content of leucite, and Mg-number (100 Mg/(Mg+Fe2+)) of olivine. The results demonstrate that the liquidus phases of the Gaussberg rocks crystallized atfO2 slightly below that of the NNO buffer. Application of the results to other lamproites indicates that they began to crystallize at oxygen fugacities varying from well above NNO (Leucite Hills) to around MW (West Kimberley and the Spanish fortunites). The Gaussberg olivine leucitite contains leucite cores poor in ferric iron with rims richer in ferric iron, indicating oxidation during emplacement. The ferric value of spinel is very sensitive to changes in oxygen fugacity and recognizing that some lamproitic magmas are known to contain diamonds, it may prove to be useful as a ‘diamond survival indicator’. The preservation of diamonds in lamproitic rocks will depend critically onfO2: diamonds are not likely to be preserved in rocks which reach the surface as liquids atfO2 near NNO or above.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 122 (1995), S. 79-96 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract  We have investigated new samples from the Gees mantle xenolith suite (West Eifel), for which metasomatism by carbonatite melt has been suggested. The major metasomatic change is transformation of harzburgites into phlogopite-rich wehrlites. Silicate glasses are associated with all stages of transformation, and can be resolved into two major groups: a strongly undersaturated alkaline basanite similar to the host magma which infiltrated the xenoliths during ascent, and Si-Al-enriched, variably alkaline glass present exclusively within the xenoliths. Si-Al-rich glasses (up to 72 wt% SiO2 when associated with orthopyroxene (Opx) are usually interpreted in mantle xenoliths as products of decompressional breakdown of hydrous phases like amphibole. In the Gees suite, however, amphibole is not present, nor can the glass be related to phlogopite breakdown. The Si-Al-rich glass is compositionally similar to glasses occurring in many other xenolith suites including those related to carbonatite metasomatism. Petrographically the silicate glass is intimately associated with the metasomatic reactions in Gees, mainly conversion of harzburgite orthopyroxene to olivine + clinopyroxene. Both phases crystallize as microlites from the glass. The chemical composition of the Si-Al-enriched glass shows that it cannot be derived from decompressional melting of the Gees xenoliths, but must have been present prior to their entrainment in the host magma. Simple mass-balance calculations, based on modal analyses, yield a possible composition of the melt prior to ascent of the xenoliths, during which glass + microlite patches were modified by dissolution of olivine, orthopyroxene and spinel. This parental melt is a calc-alkaline andesite (55–60 wt% SiO2), characterized by high Al2O3 (ca. 18 wt%). The obtained composition is very similar to high-alumina, calc-alkaline melts that should form by AFC-type reactions between basalt and harzburgite wall rock according to the model of Kelemen (1990). Thus, we suggest that the Si-Al-enriched glasses of Gees, and possibly of other suites as well, are remnants of upper mantle hybrid melts, and that the Gees suite was metasomatized by silicate and not carbonatite melts. High-Mg, high-Ca composition of metasomatic olivine and clinopyroxene in mantle xenoliths have been explained by carbonatite metasomatism. As these features are also present in the Gees suite, we have calculated the equilibrium Ca contents of olivine and clinopyroxene using the QUI1F thermodynamical model, to show that they are a simple function of silica activity. High-Ca compositions are attained at low a SiO2 and can thus be produced during metasomatism by any melt that is Opx-undersaturated, irrespective of whether it is a carbonatite or a silicate melt. Such low a SiO2 is recorded by the microlites in the Gees Si-Al-rich glasses. Our results imply that xenolith suites cannot confidently be related to carbonatite metasomatism if the significance of silicate glasses, when present, is not investigated.
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  • 5
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract New experimental amphibole/melt partition coefficients from a variety of geologically relevant amphibole (pargasite, kaersutite, and K-richterite) and melt compositions obtained under conditions of interest to upper-mantle studies are combined with the results of X-ray single-crystal structure refinement. The ideal cation radii (r0), calculated using the lattice-site elastic-strain model of Blundy and Wood (1994) under the hypothesis of complete REE (rare earth elements) ordering at [8]M4, mostly differ significantly from those obtained from both the structure refinement and the ionic radius of [8]Ca2+. Heavier REE may also strongly deviate from the parabolic trends defined by the other REE. On the basis of the crystal-chemical knowledge of major-element site-preference in amphibole and the occurrence of two sites with different co-ordination within the M4 cavity (M4 for Ca and Na, M4′ for Fe2+ and Mg), we propose a new model for REE incorporation. LREE order at the [8]M4 site, whereas HREE prefer the M4′ site with lower co-ordination in amphiboles with a significant cummingtonite component, and may also enter the M2 octahedron, at least in richterite. This more complex model is consistent with the observed Amph/LD, and drops the usual assumption that REE behave as a homogeneous group and order at the M4 site. The availability of multiple crystal-chemical mechanisms for REE3+ incorporation explains why measured and estimated Amph/LDHREE may differ by up to one order of magnitude. When REE enter two different sites within the same cavity, a fit performed on the basis of a single curve may appear correct, but the values obtained for r0 are biased towards those of the dominant site, and the Young's modulus is underestimated. When REE are incorporated in multiple sites in different cavities, the observed pattern cannot be reduced to a single curve, and the partition coefficients of heavy REE would be strongly underestimated by a single-site fit. The simplistic assumption that REE occupy a single site within the amphibole structure can thus substantially bias predictive models based on the elastic-strain theory. Our combined approach allows linkage between fine-scale site preference and the macroscopic properties of minerals and provides more reliable predictive models for mineral/melt partitioning. After the possible site-assignments have been identified, the shape of the Onuma curves constructed from accurately determined Amph/LDREE now allows the active mechanisms for REE incorporation in amphiboles to be recognised even where site populations are not available. The REE preference for polyhedra with smaller size and lower co-ordination than those occupied by Ca invalidates the general idea that Ca acts as a “carrier” for REE.
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  • 6
    Publication Date: 2016-07-01
    Print ISSN: 0022-3530
    Electronic ISSN: 1460-2415
    Topics: Geosciences
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  • 7
    Publication Date: 2012-04-25
    Description: High-Mg ultrapotassic volcanic rock occurrences of lamproitic affinity are exposed in southwestern Anatolia, mostly within the Menderes Massif. From north to south the lamproitic volcanism shows increasingly younger ages ranging from 20 to 4 Ma. Volcanism is contemporaneous with more voluminous shoshonitic, high-K calc-alkaline, and ultrapotassic magmatic activity in the Simav–Selendi, Usak, Kirka, Köroglu, Afyon and Isparta–Gölcük areas. The southward decrease in the age of the volcanism correlates with changes in geochemical composition, particularly a decrease in 87 Sr/ 86 Sr, 207 Pb/ 204 Pb, Zr/Nb and Th/Nb, and an increase in 143 Nd/ 144 Nd, 176 Hf/ 177 Hf, 206 Pb/ 204 Pb, 208 Pb/ 204 Pb and Ce/Pb, thus delineating a systematic change from orogenic (crust-like) to anorogenic (convecting mantle-like) signatures. Rare earth element compositions of clinopyroxene phenocrysts demonstrate an increasing role for residual garnet for locations in the central parts of the Menderes Massif, indicating a lithosphere thickness greater than 80 km. In contrast, K 2 O abundances remain nearly constant at around 7%, indicating buffering by phlogopite in the mantle source. Magma genesis in southwestern Anatolia is controlled by post-collisional extensional events initiated after major lithospheric thickening. Geochemical constraints suggest that the mantle source experienced two main geodynamic stages. The first stage caused ultradepletion of the mantle and subsequent metasomatic enrichment, which allowed coupling of the geochemical signatures of ultradepleted harzburgite with those of crust-derived sediments. This happened during the final closure stages of the southern Neotethys Ocean and the accretion of forearc oceanic lithosphere (island-arc type), as shallowly subducted material to the Anatolian lithosphere. The second stage is post-collisional, and is related to the collapse of the orogenic belt and the development of extension-related horst and graben structures. This stage is concurrent with the initiation of a thermal anomaly originating from a gap, identified by seismic tomography, in the subducted slab under western Anatolia. We propose that the lithospheric mantle underwent intense ‘asthenospherization’ owing to lithosphere–asthenosphere interaction, caused by the southward expansion of this gap during slab roll-back. The geochemical resemblance of the lamproites to more voluminous, contemporaneous shoshonitic magmas implies their derivation from a heterogeneous mantle source that had been affected by similar processes. These mantle processes may be closely associated with the major episode of uplift in the Menderes Massif.
    Print ISSN: 0022-3530
    Electronic ISSN: 1460-2415
    Topics: Geosciences
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  • 8
    Publication Date: 2011-07-24
    Description: Redox melting refers to any process by which melt is generated by the contact of a rock with a fluid or melt with a contrasting oxidation state. It was originally applied to melting owing to the oxidation of reduced CH 4 - and H 2 -bearing fluids in contact with more oxidized blocks in the mantle, particularly recycled crustal blocks. This oxidation mechanism causes an increase in the activity of H 2 O by the reaction of CH 4 with O 2 , and the increased a H 2 O causes a rapid drop in the solidus temperature, and is here termed hydrous redox melting (HRM). Recently, a second redox melting mechanism (carbonate redox melting; CRM) has been discovered that operates in more oxidized conditions, and may post-date the first mechanism in the same geographical area, explaining the sequence of igneous rock types from lamproites to ultramafic lamprophyres that occurs during the development of rifts through cratons. The CRM mechanism relies on the oxidation of solid carbon as graphite or diamond that has accumulated in the lithosphere over time. The solidus temperature for rocks with both CO 2 and H 2 O is lower than in conditions with H 2 O alone; it does not occur at depths less than 65 km, but has recently been confirmed experimentally to depths of at least 200 km. Melts produced by HRM are not SiO 2 -undersaturated, even at depths of 200 km, and may often resemble lamproites or SiO 2 -rich picrites, whereas melts produced by CRM are always SiO 2 -undersaturated and range from carbonatitic to ultramafic lamprophyric or melilititic with increasing degree of melting. The operation of redox melting may be more common than has been recognized because the oxidation state of the upper mantle is not uniform as a function of depth, geodynamic setting or geological time. The general decrease of oxygen fugacity ( f O 2 ) of c . 0·7 log units per 1 GPa pressure increase dictates that rapidly subducted oceanic lithosphere will be considerably more oxidized than ambient mantle peridotite at depths of 200–300 km. Hydrothermal alteration (serpentinization), addition of continental or carbonate sediments, and dehydration reactions during subduction all contribute to the heterogeneity of oxidation states in the subducted slab, which may vary over 6 log units; this raises the potential for redox reactions on local and regional scales. The oceanic lithosphere has a lower average f O 2 than either continental or cratonic mantle lithosphere at a given depth, so that the HRM mechanism dominates in recycled blocks and at the base of the continental lithosphere. The higher thermal gradients dictate that HRM is more common in the modern Earth beneath ocean islands and in upwelling mantle currents than in subduction zones. The oxidation state of the mantle is often described as having been constant since 3·5 Ga, but this overlooks the bias towards continental samples. Redox melting of oxidized recycled blocks (at approximately the fayalite–magnetite–quartz buffer) in the mantle was not important in the Hadean and Archaean, as it had to await the gradual oxidation of the mantle and the establishment of the subduction process, as well as the stabilization of the continents. The lack of CRM explains the lack of carbonatites before 2·7 Ga. However, the lower f O 2 of the Archaean asthenosphere and higher volatile contents caused more prevalent HRM in the Hadean and Archaean mantle. Degassing is controlled by solubility of volatile species in melts, which are H 2 O-rich but C-poor in reducing conditions. Silicate melts under reduced conditions contain much less carbon but more nitrogen than melts in the modern mantle, arguing for a nitrogen-rich, CO 2 -poor early atmosphere.
    Print ISSN: 0022-3530
    Electronic ISSN: 1460-2415
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  • 9
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    Unknown
    Geological Society of America (GSA)
    In: Geology
    Publication Date: 2017-04-12
    Description: The generation of strongly potassic melts in the mantle is generally thought to require the presence of phlogopite in the melting assemblage. In the Mediterranean region, trace element and isotope compositions indicate that continental crustal material is involved in the generation of many potassium-rich lavas. This is clearest in ultrapotassic rocks like lamproites and shoshonites, for which the relevant chemical signals are less diluted by extensive melting of peridotite. Furthermore, melting occurs here in young lithosphere, so the continental crust was not stored for a long period of time in the mantle before reactivation. We have undertaken two types of experiments to investigate the reaction between crust and mantle at 1000–1100 °C and 2–3 GPa. In the first, continental crustal metasediment (phyllite) and depleted peridotite (dunite) were juxtaposed as separate blocks, whereas in the second, the same rock powders were intimately mixed. In the first series, a clear reaction zone dominated by orthopyroxene was formed between dunite and phyllite but no hybridized melt could be found, whereas analyzable pools of hybridized melt occurred throughout the charges in the second series. Melt compositions show high abundances of Rb (100–220 ppm) and Ba (400–870 ppm), and consistent ratios of Nb/Ta (10–12), Zr/Hf (34–42), and Rb/Cs (28–34), similar to bulk continental crust. These experiments demonstrate that melts with as much as 5 wt% K 2 O may result from reaction between melts of continent-derived sediment and depleted peridotite at shallow mantle depths without the need for phlogopite or any other potassic phase in the residue.
    Print ISSN: 0091-7613
    Electronic ISSN: 1943-2682
    Topics: Geosciences
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  • 10
    Publication Date: 2014-06-28
    Description: We report results of a laser-ICP-MS investigation of trace element contents in the main constituent minerals of an amphibole-bearing migmatite from the Variscan orogen in northeastern Sardinia. The migmatite is associated with migmatised orthogneiss and Al-silicate-bearing pelitic migmatites. The protolith of the amphibole-bearing migmatite was a mid-Ordovician igneous rock of intermediate composition characterised by a biotite + plagioclase + quartz assemblage. The migmatite consists of mesosomes and tonalitic (or, less frequently, granodioritic) leucosomes, characterised by amphibole crystals (potassian ferropargasite) up to 2 cm in size. The tonalitic leucosomes are made up of quartz, plagioclase, ±K-feldspar, biotite, ±amphibole, garnet. The mesosomes are foliated rocks made up of the same minerals with different modal proportions. In leucosomes, amphibole is the most abundant mafic mineral, occurring as euhedral crystals rich in plagioclase, quartz, and small garnet inclusions. Garnet occurs as corroded and fractured grains in the matrix or within the amphibole. Zircon forms euhedral bipyramidal grains up to a few hundreds of micrometres in size. Some amphibole rims have higher REE and negative Eu anomalies whereas cores exhibit lower REE and positive Eu anomalies. Garnet has strongly fractionated REE patterns with chondrite-normalised abundances up to 2000 for HREE. Plagioclase has flat REE patterns with pronounced positive Eu anomalies. Zircon displays fractionated REE patterns with HREE enrichment, LREE depletion, positive anomalies for Ce and negative ones for Eu. Monazite shows high REE abundances, LREE enrichment, HREE depletion and negative Eu anomalies. Garnet is mostly a restitic phase, as indicated by significant variation in HREE concentrations between grains in the mesosome, the absence of a noticeable Eu anomaly, and Y depletion in the leucosomes as compared to the mesosomes. In the leucosomes and mesosomes, the cores of zoned amphibole are characterised by positive Eu anomalies: these crystallised from or in the presence of melt produced by anatexis of the original Bt + Pl + Qtz protolith. Adjacent rims with negative Eu-anomalies developed in coexistence with a Eu-depleted melt that had experienced plagioclase fractionation.
    Print ISSN: 0935-1221
    Electronic ISSN: 1617-4011
    Topics: Geosciences
    Published by Schweizerbart
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