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Titel Experimental study of the P-T stability of phlogopite in metasomatised peridotite with varying H2O contents in the deep cratonic lithosphere
VerfasserIn Greg Yaxley, Anja Rosenthal
Konferenz EGU General Assembly 2014
Medientyp Artikel
Sprache Englisch
Digitales Dokument PDF
Erschienen In: GRA - Volume 16 (2014)
Datensatznummer 250090414
Publikation (Nr.) Volltext-Dokument vorhandenEGU/EGU2014-4649.pdf
 
Zusammenfassung
Phlogopite is an important metasomatic, hydrous, potassic phase in peridotite from on- and off-cratonic lithospheric mantle. It is significant in petrogenesis of exotic mantle-derived magmas such as micaceous kimberlites, ultramafic lamprophyres, kamafugites, lamproites and olivine basanites[1-6]. Along with other potassic hydrous agents (fluids/melts), phlogopite is a major repository for potassium, H2O and F in K-enriched peridotitic mantle down to ~200 km or more (≈6 GPa[7-10]). Although some recent studies delineated phlogopite stability in peridotite at a given bulk H2O content1[1,8-10,12], we lack experimental investigations close to the limits of phlogopite stability in a model mantle composition enriched in K (i.e. by metasomatic agents) with varying amounts of H2O over a pressure range of 4-6 GPa, i.e. from ≈120 to 200 km deep. Variations in the %H2O available however determine the shape and location of the solidus, and hence the onset of partial melting of a K-enriched mantle enriched[8,13]. Our experimental base composition (HPK2) is fertile peridotite + 0.5wt% K2O. Mixes HPK2-0 and HPK2-13 were prepared by blending powdered high purity oxides or carbonates of Si, Ti, Al, Mg, Cr, Ni, Mn, Ca, Na and K. Mg(OH)2 was included in HPK2-13 to produce a mix with 13wt% H2O. HPK2-0 is anhydrous. HPK2-0 and HPK2-13 were blended to create 3 additional mixes with identical compositions but varying H2O contents, nominally 0.2, 2 and 5wt% H2O. Experiments were run in Au, AuPd or graphite (in Pt) capsules at 4-6 GPa and 1050-1350°C. Run products were analysed by EDS on a SEM. Experiments crystallized assemblages of olivine + orthopyroxene ± clinopyroxene ± garnet ± rutile ± phlogopite. We define the temperature stability limit of phlogopite in potassic-peridotite between 1200 and 1250°C at 4 GPa and <1300°C at 5 GPa, consistent with interpolation of data from previous lower[1] and higher pressure[14] investigations. We also demonstrate the leaching effect of large excesses of hydrous fluid. Sub-solidus runs with 13wt% H2O, at P-T conditions within the phlogopite stability field at low %H2O, are phlogopite and clinopyroxene-free, indicating that hydrous-fluids under these conditions may transport significant Na, K, Ca, Al and other solutes[8,12]. References 1 Mengel, K. & Green, D. H. Geol. Soc. Aust. Spec. Publ. 14, 571-581 (1989). 2 Mitchell, R. H. Kimberlites, orangeites, and related rocks. (Plenum Press, 1995). 3 Foley, S. Lithos 28, 435-453 (1992). 4 Prelevic, D. et al. Terra Nova 22, 443-452 (2010). 5 Tappe, S. et al. Earth Planet Sci Lett 256, 433-454 (2007). 6 Rosenthal, A., et al. Earth Planet Sci Lett 284, 236-248 (2009). 7 Foley, S. Geochim Cosmochim Acta 55, 2689-2694 (1991). 8 Green, D. H., et al. Nature 467, 448-497 (2010). 9 Konzett, J., et al. Contrib Mineral Petrol 163, 277-296 (2012). 10 Konzett, J. & Ulmer, P. J Petrol 40, 629-652 (1999). 11 Fumagalli, P., et al. Contrib Mineral Petrol 158, 723-737 (2009). 12 Kovács, I. et al. J Petrol 53, 2067-2093 (2012). 13 Niida, K. & Green, D. H. Contrib Mineral Petrol 135, 18-40 (1999). 14 Luth, R. Am Mineral 82, 1198-1209 (1997).