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1 GeoForschungsZentrum Potsdam, Division 4, Telegrafenberg, D-14473 Potsdam, Germany
2 Institut für Geowissenschaften der Technischen Universität Braunschweig, Abteilung für Mineralogie, Gausstrasse 28/29, D-38106 Braunschweig, Germany
Correspondence: * E-mail: feenstra{at}gfz-potsdam.de
Li-H-rich zincostaurolite locally formed at a metabauxite-marble contact along the eastern coast of Samos during early Alpine high-P, low-T metamorphism. The staurolite, which probably grew from gahnite, cookeite, kaolinite/pyrophyllite, diaspore, and minor Fe-oxide, occurs as prismatic crystals (up to several mm long) in a calcite matrix. It has an unusual composition with 7.512.9 wt% ZnO, 1.04.9 wt% FeO, 0.660.82 wt% Li2O, up to 2.6 wt% NiO and 0.59 wt% CoO, and
0.32 wt% MgO. Calculated structural formulae point to high H2O contents (
4.14 H atoms per 48 oxygen atoms). During late-Alpine uplift of the Samos rocks, the staurolite was, at greenschist-facies conditions, variably replaced by bluish cobaltoan gahnite (XZn > 0.82), white Na-Ca-Li mica, Ni-rich chlorite (XNi = 0.420.59), zincohögbomite (XZn = 0.680.80), diaspore, and Fe-(hydr)oxide. Detailed EMP work and determination of Li in staurolite and mica by SIMS indicates systematic Zn-Fe-Mg-Ni-Co-Li partitioning between staurolite and its decomposition products, implying local-scale chemical equilibrium. Balanced reaction equations based on mineral-chemical data indicate that the breakdown of staurolite occurred largely isochemically with only introduction of water, Na, and Ca into the reacting system. The breakdown of high-P staurolite during uplift and decompression is thought to be related to the sensitivity of its complex crystal chemistry to changes in physico-chemical conditions.
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