Eclogite-facies shear zones--deep crustal reflectors?

Strongly foliated eclogite-facies rocks in 30-150 m thick shear zones of Caledonian age occur within a Grenvillian garnet granulite-facies gabbro-anorthosite terrain in the Bergen Arcs of Norway. The predominant eclogite-facies mineral assemblages in the shear zones are omphacite + garnet + zoisite + kyanite in gabbroic anorthosite and omphacite + garnet in gabbro. Eclogite-facies rocks in shear zones are generally fine-grained; alternating omphacite/garnet- and kyanite/clinozoisite-rich layers define gneissic layering. A strong shape preferred orientation of omphacite, kyanite, and white mica (phengitic muscovite and/or paragonite) define the foliation. The anorthositic eclogites show omphacite b-axis maxima approximately normal to the foliation and c-axis girdles within the foliation plane. P-wave velocities (Vp) determined at confining pressures to 600 MPa for samples from eclogite-facies shear zones range from 8.3 to 8.5 km s-1 and anisotropy ranges from 1 to 7%. The few samples with more pronounced anisotropy tend to be approximately transversely isotropic with minimum velocities for propagation directions normal to foliation and maximum velocities for propagation directions parallel to foliation. The fast propagation direction lies within the c-axis girdles (parallel to foliation) and the slow propagation direction is parallel to the b-axis concentration (normal to foliation) in samples for which omphacite crystallographic preferred orientation was determined. Vp for the granulite-facies protoliths average about 7.5 km s-1. High calculated reflection coefficients for these shear zones, 0.04-0.14, indicate that they are excellent candidates for deep crustal reflectors in portions of crust that experienced high-pressure conditions but escaped thermal reactivation.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/31633/1/0000567.pd

Characterization of olivine fabrics and mylonite in the presence of fluid and implications for seismic anisotropy and shear localization

The Lindås Nappe, Bergen Arc, is located in western Norway and displays two high-grade metamorphic structures. A Precambrian granulite facies foliation is transected by Caledonian fluid-induced eclogite-facies shear zones and pseudotachylytes. To understand how a superimposed tectonic event may influence olivine fabric and change seismic anisotropy, two lenses of spinel lherzolite were studied by scanning electron microscope (SEM) and electron back-scattered diffraction (EBSD) techniques. The granulite foliation of the surrounding anorthosite complex is displayed in ultramafic lenses as a modal variation in olivine, pyroxenes, and spinel, and the Caledonian eclogite-facies structure in the surrounding anorthosite gabbro is represented by thin (<1 cm) garnet-bearing ultramylonite zones. The olivine fabrics in the spinel bearing assemblage were E-type and B-type and a combination of A- and B-type lattice preferred orientations (LPOs). There was a change in olivine fabric from a combination of A- and B-type LPOs in the spinel bearing assemblage to B- and E-type LPOs in the garnet lherzolite mylonite zones. Fourier transform infrared (FTIR) spectroscopy analyses reveal that the water content of olivine in mylonite is much higher (approximately 600 ppm H/Si) than that in spinel lherzolite (approximately 350 ppm H/Si), indicating that water caused the difference in olivine fabric. Fabric strength of olivine gets weaker as the grain size reduced, and as a result, calculated seismic properties for the two deformation stages reveal that P- and S-velocity anisotropies are significantly weaker in the mylonite. Microtextures and LPO data indicate that the deformation mechanism changed from dominant dislocation creep in spinel lherzolite to dislocation creep accompanied by grain-boundary sliding in mylonite. Shear localization in the mylonite appears to be originated from the grain size reduction through (1) enhanced dynamic recrystallization of olivine in the presence of water and (2) Zener pinning of clinopyroxene or (3) by ultracomminution during the pseudotachylyte stage

Brittle-ductile microfabrics in naturally deformed zircon : deformation mechanisms and consequences for U-Pb dating

We present an electron backscatter diffraction, cathodoluminescence, and radiogenic U-Pb dating study of large zircon grains (0.8-1.5 mm) that show evidence of intracrystalline deformation, fracturing, grain size reduction and a large spread in U-Pb ages. The samples are from an amphibolite facies deformation zone within granulite facies anorthositic rocks (Bergen Arc, Norway). Large zircon grains show three main lattice distortion types: (I) distortions with rotations around and an orientation change of -0.3 °/μm subparallel to (100); (II) highly distorted, half circular shaped zones located at grain edges with at least 0.8-1 °/μm distortions; and (III) low-angle boundary networks forming deformation zones up to 100 μm wide. Types II and III distortions exhibit significant disturbances of the otherwise homogeneous CL signature. Crystal plastic deformation with the slip system [010] (100) resulted in type I distortions. Stress concentrations at grain contacts between rheologically hard grains caused localized crystal plastic deformation with minor amount of microfracturing forming type II distortions. Type III distortions formed by crystal plastic deformation often associated with inclusions using several slip systems. Distortions of types I and II show minor and moderate resetting of the original ca. 900 Ma zircon grains, respectively, due to enhanced pipe diffusion along dislocation walls. In type II distortions, accelerated lattice diffusion through the highly distorted crystal lattice, combined with exceptionally high boundary to volume ratio, caused significant chemical disturbance and age resetting to 410 Ma. Fine-grained aggregates contain grains with low internal deformation and an oscillatory zoned CL signature (Z-grains) or high internal deformation and a disturbed CL signature (D-grains). Z- and D-grains are interpreted to have formed by heterogeneous nucleation and growth, and fracturing along strain-hardened low-angle boundaries present within types I and II, respectively. Z-grains show a clustered chemical signature with a 437 ±11 Ma age interpreted to directly date the Caledonian amphibolite facies reworking.20 page(s

Olivine pseudomorphs after serpentinized orthopyroxene record transient oceanic lithospheric mantle dehydration (Leka Ophiolite Complex, Norway)

We examine the partial survival of high-temperature mantle microstructures throughout multi-stage hydration- and dehydration-mediated pseudomorphism at differing pressure-temperature-fluid conditions. Throughout the harzburgitic mantle section of the Leka Ophiolite Complex (Norway), finite domains of parallel olivine encompassed by mesh-textured olivine resembling 'perfectly cleaved' olivine grains were identified. Crystallographic orientation mapping, combined with micro-computed tomography, reveals that the parallel olivine grains are highly misoriented (up to 90°) with no crystal-preferred orientation, despite remaining parallel in three dimensions. Parallel olivine grains exhibit free dislocations with low dislocation density, whereas within mesh-textured olivine dislocations are aligned into walls. MnO is enriched (up to 1·8 wt %) and NiO depleted (0·21 ± 0·24 wt %) within parallel olivine grains compared with mesh-textured olivine (0·29 ± 0·14 wt % MnO; 0·38 ± 0·19 wt % NiO). Clinopyroxene lamellae that are crystal-plastically deformed occur sandwiched in lizardite layers between every parallel olivine grain or fully enclosed within olivine. Al₂O₃ and Cr₂O₃ concentrations of clinopyroxene lamellae (2·09 ± 0·88 wt % Al₂O₃; 0·79 ± 0·27 wt % Cr₂O₃) overlap with those of primary clinopyroxene grains (2·43 ± 0·69 wt % Al₂O₃; 0·83 ± 0·36 wt % Cr₂O₃) and are distinctly different from those of secondary diopside found within the parallel olivine domains. Intragranular serpentine inclusions (XMg = 0·95 ± 0·01), displaying elevated Al₂O₃ (3·92 ± 4·10 wt %) and Cr₂O₃ (0·78 ± 0·82 wt %) concentrations, are exclusively found within parallel olivine grains. Lizardite (XMg = 0·92 ± 0·02) within the domains originates from hydration of parallel olivine and compositionally overlaps with mesh-texture lizardite. Antigorite (XMg = 0·95 ± 0·01) replaces both types of olivine grains. Whole-rock compositions indicate a harzburgitic composition; however, microstructural and chemical observations and the current absence of primary orthopyroxene suggest that the precursor silicate of every parallel olivine domain was a single orthopyroxene grain that was initially serpentinized and later dehydrated to result in the present microstructure. Although desilicification is necessary during the transformation of orthopyroxene to olivine via a bastite stage, calculations based on whole-rock compositions imply that the released SiO₂(aq) was mobile only over micrometer to centimeter scales, reacting with the surrounding olivine directly to form serpentine. Crosscutting relationships and serpentine compositions imply that dehydration occurred prior to the now evident lizardite- and antigorite-serpentinization. Comparison with the regional geological setting indicates that dehydration may have occurred transiently within the oceanic lithosphere prior to obduction.26 page(s

Microstructural Evolution of Amphibole Peridotites in Åheim, Norway, and the Implications for Seismic Anisotropy in the Mantle Wedge

The microstructure of amphibole peridotites from Åheim, Norway were analyzed to understand the evolution of the lattice-preferred orientation (LPO) of olivine throughout the Scandian Orogeny and its implication for the seismic anisotropy of the subduction zone. The Åheim peridotites had a porphyroclastic texture and some samples contained an abundant amount of hydrous minerals such as tremolite. Detailed microstructural analysis on the Åheim peridotites revealed multiple stages of deformation. The coarse grains showed an A-type LPO of olivine, which can be interpreted as the initial stage of deformation. The spinel-bearing samples showed a mixture of B-type and C-type LPOs of olivine, which is considered to represent the deformation under water-rich conditions. The recrystallized fine-grained olivine displays a B-type LPO, which can be interpreted as the final stage of deformation. Microstructures and water content of olivine indicate that the dominant deformation mechanism of olivine showing a B-type LPO is a dislocation creep under water-rich condition. The observation of the B-type LPO of olivine is important for an interpretation of trench-parallel seismic anisotropy in the mantle wedge. The calculated seismic anisotropy of the tremolite showed that tremolite can contribute to the trench-parallel seismic anisotropy in the mantle wedge

From peridotite to fuchsite bearing quartzite via carbonation and weathering: with implications for the Pb budget of continental crust

Abstract Extensive carbonation of peridotite results in listvenite, a rock composed of magnesite and quartz. At Gråberget, Røros, SE-Norway, a variably serpentinized peridotite body, surrounded by the Røros schists, a former abyssal sediment displays all stages of transformation of peridotite to quartzite. In this paper we record the sequence of steps in this process by combining the observation of mineral assemblages, textural relationships and geochemistry, and variations in Pb isotopic compositions. Initial serpentinization, a stage that also involved an enrichment in fluid-mobile elements (Pb, Sb and As), was followed by carbonation through CO 2 fluids that formed soapstone, and eventually listvenite. The listvenite grades by decreasing amounts of carbonates into fuchsite bearing quartzite. The carbonates dissolved during supergene alteration and formed pores coated with oxides of Fe, Mn and Ni resulting in a brown rock color. The quartzite displays porous stylolites enriched in Pb, As and Sb and fuchsite with porous chromite grains as the only relicts of the original mineralogy in the peridotite. The dissolution of the carbonate occurred at oxidizing conditions at temperatures below 150 °C, where the solubility of magnesite is higher than that of quartz. Formation of quartzite from peridotite is supported by low REE contents and lack of zircons in the two rock types. The transformation involved enrichment of Pb, coupled with the elimination of Mg and enrichment of Si. This chemical fractionation and selective transfer of elements to the continents is an important mechanism and needs to be taken into account in models of continental evolution

Ophicarbonates of the Feragen Ultramafic Body, central Norway

The carbonation of ultramafic rocks is a common alteration process in ophiolites and can occur in various settings. We provide the first detailed description of the carbonated peridotites (ophicarbonates) of the Feragen Ultramafic Body, central Norway, which have unusually variable compositions and microstructures. Lithologies range from pervasively carbonated serpentinites through carbonated serpentinite breccias to carbonated ultramafic conglomerates. Carbonate phases are Ca-carbonate, magnesite and dolomite. Some breccias are also cemented by coarsegrained brucite. This variability records strong variations in fluid chemistry and/or pressure and temperature conditions, both spatially and temporally. By analysing these altered ultramafic rocks using field relationships, optical microscopy, electron microprobe analysis and oxygen and carbon isotope compositions, we elucidate the history of the Feragen Ultramafic Body in more detail and emphasise the importance of deformation for the extent and type of alteration