COMPORTEMENT DES RADIOCHRONOMETRES Rb/Sr, Ar/Ar ET Sm/Nd AU COURS DU METAMORPHISME : CAS DES ECLOGITES DE L'ARC DE BERGEN (NORVEGE)

Understanding chemical element mobility during high-pressure metamorphism is paramount to the knowledge of eclogite transformation. In particular, the role of deformation and fluid circulations appears essential. In order to better decipher this role, we investigated eclogitic samples from the Lindås Nappe in the Bergen arcs (Norwegian Caledonides) which are related to a fluid/deformation metamorphic event. This study, based on detailed microtextural investigations, coupled with extensive in-situ (EMPA and LA-ICP-MS) and mineral fraction (ICP-MS) major and trace element analyses, demonstrates a contrasting behaviour during the eclogite and the amphibolite transformations. A single mineral species from the eclogite facies (i.e. phengite and epidote) depicts various chemical features depending on its textural location at thin section scale. The correlation with the mineralogical reaction occurring in each textural site demonstrates that the variations in composition are inherited from the chemistry of precursor minerals. Thus, the composition of eclogitic minerals is locally controlled by the composition of few hundred-micron microdomains. On the contrary, alteration phases of the amphibolite facies (symplectite and calcic amphibole) display clear enrichment in LILE, Pb, Sr and LREE compared to their precursor minerals (omphacite and garnet). This supports that the transport of elements at hand-sample scale was enhanced during the retrogression and elements were efficiently delocalised from one textural site to another. The contrasting behaviour for element mobility between peak eclogitic metamorphism and retrogression can be explained in term of rate process and fluid/deformation activity. During eclogitisation, deformation allows the formation of textural and mineralogical microdomains. Contemporaneously the fluid circulation favours the development of heterogeneities by transport of elements in excess towards areas protected from deformation where quartz lenses crystallise including phengites. This, together with very fast recrystallisation of eclogitic minerals, results in a heterogeneous redistribution of elements at a sample scale and to a chemical disequilibrium between different microdomains of hundred-micron size. During retrogression in the amphibolite facies coeval with long term ductile deformation, the fluids act as an efficient vector to redistribute the elements from a given textural site to another and, therefore, permit to reach a new chemical equilibrium between the crystallising phases at a hand-sample scale. Rb/Sr, 40Ar/39Ar and Sm/Nd isotopic data are reported in Caledonian eclogites from the Lindås Nappe, Bergen Arcs, Norway, in order to investigate processes controlling isotopic equilibrium at mineral scale in polymetamorphic rocks. The Bergen Arcs exposes Sveconorwegian c. 950-930 Ma granulites, partially overprinted by Caledonian eclogite-facies metamorphism at c. 425 Ma and amphibolite-facies metamorphism at c. 410 Ma. Geochemical and Rb-Sr data from more than ten phengite fractions separated from one sample reflect the composition of the microdomain (a few hundred-microns in size) in which phengite crystallized. Phengite crystallized after garnet or plagioclase by dissolution-precipitation processes yield apparent age between 700 and 600 Ma. At the time of their crystallization, these phengites inherited the isotopic composition of their precursor minerals, at a microdomain scale. Phengite from quartz veins, which crystallized from elements mobilized by the circulating fluid, yield an age closer to the eclogite-facies metamorphic age. The closed system evolution of the eclogitizing fluid, the segregation of textural and reactional microdomains, the high Sr content of the studied phengite and the short duration of the recrystallization processes (