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We investigated rutile needles with a clear shape preferred orientation in garnet from (ultra-) high pressure metapelites from the Kimi Complex of the Greek Rhodope by electron microprobe, Electron Back Scatter Diffraction and TEM-techniques. A definite though complex crystallographic orientation relationship between the garnet host and rutile was identified in that Rt[001] is either parallel to Grt<111> or describes cones with opening angle 27.6° around Grt<111>. Each Rt[001] small circle representing a cone on the pole figure displays six maxima in the density plots. This evidence together with microchemical observations in TEM, when compared to various possible mechanisms of formation, corroborates a precipitate origin. A review of exchange vectors for Ti-substitution in garnet indicates that rutile formation from garnet cannot occur in a closed system. It requires that components are exchanged between the garnet interior and the rock matrix by solid state diffusion, a process we refer to as "open system precipitation" (OSP). The kinetically most feasible reaction of this type will dominate the overall process. The perhaps most efficient reaction involves internal oxidation of Fe 2+ to Fe 3+ and transfer from the dodecahedral to the octahedral site just vacated by Ti 4+ : 6

This study combines new data on tectonostratigraphy, macrostructures and microstructures, petrology, and geochronology to propose a comprehensive model for the tectonometamorphic evolution of the Rhodope orogen from the Jurassic to the early Paleogene. Rocks from two study areas in the central and eastern Greek Rhodope represent a continental suture zone (Rhodope Suture Zone), with the included material most likely forming an extensional allochthon south of the European continent during Permo/Triassic times that was subsequently subducted beneath Europe in the Early Jurassic (≥180 Ma). On the basis of comparable metamorphic ages and coherent structures but differences in metamorphic conditions and lithologies, the rocks of the Rhodope Suture Zone are subdivided into an upper and a lower part. The prograde history is linked with subduction‐related structures in the lower part (uniaxial stretching, deformation stage D1). In metapelites, the earliest stage of metamorphism recorded at circa 180 Ma occurred at least under ultrahigh‐pressure metamorphic conditions. The rocks of the upper part experienced isothermal decompression with partial anatexis. Exhumation paths of both parts differ in temperature because of the relative tectonic position within the exhuming wedge. Exhumation was forced by the Nestos Shear Zone that controlled the early phase of normal displacement by SW shearing at the base (lower part) and NE shearing on top (upper part) from the Late Jurassic to the Late Cretaceous (deformation stage D2). An intervening stage of mineral recrystallization and thermal reequilibration in the upper part was followed by a common exhumation history of both parts at pressures lower than about 12 kbar (35–40 km depth). During this stage, exhumation was controlled by southwest directed shearing and folding (deformation stage D3). Slab retreat to the south led to subsequent extension (deformation stage D4) and final exhumation coeval with the formation of basement domes, thus making the Rhodope a classic core complex juxtaposed with former structurally higher units.

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In deep and cold subduction such as that experienced by the UHP Units of the Western Alps, carbon dissolution is a relevant mechanism for carbon transfer from the slab into the mantle. The UHP impure Cal-Dol-marbles from the Dora-Maira Massif are studied to investigate the poorly known evolution of dolomite during deep subduction. Dolomite shows four stages of growth, from pre-Alpine to early-retrograde Alpine, coupled with chemical variations and distinct included mineral assemblages. To explain the evidence for growth and partial reabsorption of dolomite through HP prograde, UHP peak, and UHP early-retrograde Alpine metamorphism, a chemically simple marble (Cal, Dol, Di, Fo, and retrograde Atg, Tr, Mg-Chl) has been studied in detail. This is a preprint, the final version is subject to change, of the American Mineralogist (MSA) Cite as Authors (Year) Title. American Mineralogist, in press. (DOI will not work until issue is live.