The U-Pb and Sm-Nd dating of deep crustal rocks from the Bergen Arcs system helps resolve enigmatic aspects of the tectonic evolution of the Caledonian Orogen in western Norway and yields insights into the arrested stages of eclogite development within the granulites of the area. The U-Pb dating of zircon from one of the eclogite facies shear zones yields an upper intercept age of 945 ± 5 Ma [all errors two standard deviations (2σ)], which is similar to other zircon ages from the granulite facies protolith. The age is interpreted to represent the time of late Proterozoic (Sveconorwegian) granulite metamorphism. The U-Pb ages of sphene and epidote show that the eclogites formed early in the evolution of the Caledonian Orogen (pre-Scandian phase) at about 460 Ma. An eclogite facies quartz vein yields a Sm-Nd whole rock-garnet isochron of 440 ± 12 Ma that may reflect the onset of cooling immediately after peak eclogite facies conditions, although the Sm-Nd systematics reveal some isotopic disequilibrium within the sample. In tandem with previous 40Ar/39Ar age determinations from, an adjacent eclogite of 450 Ma for hornblende and 430 Ma for muscovite, these data indicate that < 30 Ma elapsed between formation of the eclogites and the initial stages of cooling and exhumation to at least mid-crustal levels. This corresponds to minimum cooling rates of 14 °C/m.y. The timing relations suggest that the formation and exhumation of these eclogites from the overlying Caledonian Nappe wedge in western Norway are related to an early phase of crustal subduction during or somewhat before the major phase of continent-continent collision.
The short period of time between the formation of the eclogites and the initial stages of exhumation and rapid cooling is consistent with the only partial and localized transformation of the granulite to eclogite. Isolated occurrences of eclogite within the granulite, the formation of eclogite along metasomatic fronts and the formation of hydrous eclogite facies minerals within the “dry” granulite all point to the importance of fluids in the transformation and re-equilibration of the granulite to eclogite. Together, field and isotopic data demonstrate that both the localized and limited access of fluids and the rapid cycling of continental crust through the deepest portions of the orogen to upper crustal levels resulted in the preservation of the arrested stages of eclogite formation and survival of the granulites metastably through eclogite facies conditions. 相似文献
Eclogite thermobarometry is crucial for constraining the depths and temperatures to which oceanic and continental crust subduct. However, obtaining the pressure and temperature (P–T) conditions of eclogites is complex as they commonly display high-variance mineral assemblages, and the mineral compositions only vary slightly with P–T. In this contribution, we present a comparison between two independent and commonly used thermobarometric approaches for eclogites: conventional thermobarometry and forward phase-equilibrium modelling. We assess how consistent the thermobarometric calculations are using the garnet–clinopyroxene–phengite barometer and garnet–clinopyroxene thermometer with predictions from forward modelling (i.e. comparing the relative differences between approaches). Our results show that the overall mismatch in methods is typically ±0.2–0.3 GPa and ±29–42°C although differences as large as 80°C and 0.7 GPa are possible for a few narrow ranges of P–T conditions in the forward models. Such mismatch is interpreted as the relative differences among methods, and not as absolute uncertainties or accuracies for either method. For most of the investigated P–T conditions, the relatively minor differences between methods means that the choice in thermobarometric method itself is less important for geological interpretation than careful sample characterization and petrographic interpretation for deriving P–T from eclogites. Although thermobarometry is known to be sensitive to the assumed XFe3+ of a rock (or mineral), the relative differences between methods are not particularly sensitive to the choice of bulk-rock XFe3+, except at high temperatures (>650°C, amphibole absent) and for very large differences in assumed XFe3+ (0–0.5). We find that the most important difference between approaches is the activity–composition (a–x) relations, as opposed to the end-member thermodynamic data or other aspects of experimental calibration. When equivalent a–x relations are used in the conventional barometer, P calculations are nearly identical to phase-equilibrium models (ΔP < 0.1). To further assess the implications of these results for real rocks, we also evaluate common mathematical optimizations of reaction constants used for obtaining the maximum P–T with conventional thermobarometric approaches (e.g. using the highest aGrs2 × aPrp in garnet and Si content in phengite, and the lowest aDi in clinopyroxene). These approaches should be used with caution, because they may not represent the compositions of equilibrium mineral assemblages at eclogite facies conditions and therefore systematically bias P–T calculations. Assuming method accuracy, geological meaningful Pmax at a typical eclogite facies temperature of ~660°C will be obtained by using the greatest aDi, aCel, and aPrp and lowest aGrs and aMs; garnet and clinopyroxene with the lowest Fe2+/Mg ratios may yield geological meaningful Tmax at a typical eclogite facies pressure of 2.5 GPa. 相似文献
Exhumed eclogitic crust is rare and exposures that preserve both protoliths and altered domains are limited around the world. Nominally anhydrous Neoproterozoic anorthositic granulites exposed on the island of Holsnøy, in the Bergen Arcs in western Norway, preserve different stages of progressive prograde deformation, together with the corresponding fluid‐assisted metamorphism, which record the conversion to eclogite during the Ordovician–Silurian Caledonian Orogeny. Four stages of deformation can be identified: (1) brittle deformation resulting in the formation of fractures and the generation of pseudotachylites in the granulite; (2) development of mesoscale shear zones associated with increased fluid–rock interaction; (3) the complete large‐scale replacement of granulite by hydrous eclogite with blocks of granulite sitting in an eclogitic “matrix”; and (4) the break‐up of completely eclogitized granulite by continued fluid influx, resulting in the formation of coarse‐grained phengite‐dominated mineral assemblages. P–T constraints derived from phase equilibria forward modelling of mineral assemblages of the early and later stages of the conversion to eclogite document burial and partial exhumation path with peak metamorphic conditions of ~21–22 kbar and 670–690°C. The P–T models, in combination with existing T–t constraints, imply that the Lindås Nappe underwent extremely rapid retrogressive pressure change. Fluid infiltration began on the prograde burial path and continued throughout the recorded P–T evolution, implying a fluid source that underwent progressive dehydration during subduction of the granulites. However, in places limited fluid availability on the prograde path resulted in assemblages largely consuming the available fluid, essentially freezing in snapshots of the prograde evolution. These were carried metastably deeper into the mantle with strain and metamorphic recrystallization partitioned into areas where ongoing fluid infiltration was concentrated. 相似文献
Granulite facies anorthosites on Holsenøy Island in the Bergen Arcs region of western Norway are transected by shear zones 0.1–100 m wide characterized by eclogite facies assemblages. Eclogite formation is related to influx of fluid along the shears at temperatures of c. 700d?C and pressures in excess of 1.7 GPa. Combined carbon and nitrogen stable isotope, 40Ar/36Ar, trace-element and petrological data have been used to determine the nature and distribution of fluids across the anorthosite-eclogite transition. A metre-wide drilled section traverses the eclogitic centre of the shear into undeformed granulite facies garnet-clinopyroxene anorthosite. Clinozoisite occurs along grain boundaries and microcracks in undeformed anorthosite up to 1 m from the centre of the shear and clinozoisite increases in abundance as the edge of the shear zone is approached. The eclogite-granulite transition, marked by the appearance of sodic pyroxene and loss of albite, occurs within the most highly sheared section of the traverse. The jadeite-in reaction coincides with increased paragonite activity in mica. The separation between paragonite and clinozoisite reaction fronts can be semiquantitatively modelled assuming advective fluid flow perpendicular to the shear zone. The inner section of the traverse (0.25 m wide) is marked by retrogressive replacement of omphacite by plagioclase + paragonite accompanied by veins of quartz-phengite-plagioclase. C-N-Ar characteristics of fluid inclusions in garnet show that fluids associated with precursor granulite, eclogite and retrogressed eclogite are isotopically distinct. The granulite-eclogite transition coincides with a marked change in CO2 abundance and δ13C (<36ppm, δ13C=-2% in the granulite; <180 ppm, δ13C=-10% in the eclogite). The distribution of Ar indicates mixing between influxed fluid (40Ar/36Ar > 25 times 103) and pre-existing Ar in the granulite (40Ar/36Ar < 8 times 103). δ15N values decrease from +6% in the anorthosite to +3% within the eclogite shear. The central zone of retrogressed eclogite post-dates shearing and is characterised by substantial enrichment of Si, K, Ba and Rb. Fluids are CO2-rich (δ13C ~ -5%) with variable N2 and Ar abundances and isotopic compositions. Both Ar and H2O have penetrated the underformed granulite fabric more than 0.5m beyond the granulite/eclogite transition during eclogite formation. Argon isotopes show a mixing profile consistent with diffusion through an interconnecting H2O-rich fluid network. In contrast, a carbon-isotope front coincides with the deformation boundary layer, indicating that the underformed anorthosite was impervious to CO2-rich fluids. This is consistent with the high dihedral angle of carbonic fluids, and may be interpreted in terms of evolving fluid compositions within the shear zone. 相似文献
最近在青藏高原拉萨地体新发现了一条榴辉岩带,该榴辉岩带位于冈底斯岩浆岛弧带的北缘。对该带榴辉岩的岩石地球化学特征及SmNd、RbSr同位素组成研究表明: ① 该带榴辉岩的原岩主要是一套低钾的大洋拉斑系列玄武岩,其原岩类似于典型的NMORB,源于亏损地幔; ② 该带榴辉岩样品 (87Sr/86Sr)i=0.70335~0.70457,变化范围较大,且与εNd(t)值及微量元素特征均没有好的对应关系,可能是由于该套岩石形成于大洋环境,形成后遭受了海水的蚀变作用;(3)该带榴辉岩全岩的SmNd等时线年龄为305.5±50Ma (2σ),(143Nd/144Nd)i=0.5126±0.00007 (2σ),表明该带榴辉岩可能形成于早石炭-晚二叠世,在这一时期冈底斯北缘可能存在古特提斯洋盆及古特提斯洋盆深俯冲作用。 相似文献