An experimental study on the shallow-level migmatization of ferrogabbros from the Fuerteventura Basal Complex, Canary Islands

Spectacular shallow-level migmatization of ferrogabbroic rocks occurs in a metamorphic contact aureole of a gabbroic pluton of the Tierra Mala massif (TM) on Fuerteventura (Canary Islands). In order to improve our knowledge of the low pressure melting behavior of gabbroic rocks and to constrain the conditions of migmatization of the TM gabbros, we performed partial melting experiments on a natural ferrogabbro, which is assumed as protolith of the migmatites. The experiments were performed in an internally heated pressure vessel (IHPV) at 200 MPa, 930–1150 °C at relatively oxidizing conditions. Distinct amounts of water were added to the charge.

From 930 to 1000 °C, the observed experimental phases are plagioclase (An_60–70), clinopyroxene, amphibole (titanian magnesiohastingsites), two Fe–Ti oxides, and a basaltic, K-poor melt. Above 1000 °C, amphibole is no longer stable. The first melts are very rich in normative plagioclase (>70 wt.%). This indicates that at the beginning of partial melting plagioclase is the major phase which is consumed to produce melt. In the experiments, plagioclase is stable up to high temperatures (1060 °C) showing increasing An content with temperature. This is not compatible with the natural migmatites, in which An-rich plagioclase is absent in the melanosomes, while amphibole is stable. Our results show that the partial melting of the natural rocks cannot be regarded as an “in-situ” process that occurred in a closed system. Considerable amounts of alkalis probably transported by water-rich fluids, derived from the mafic pluton underplating the TM gabbro, were necessary to drive the melting reaction out of the stability range of plagioclase. A partial melting experiment with a migmatite gabbro showing typical “in-situ” textures as starting material supports this assumption.

Crystallization experiments performed at 1000 °C on a glass of the fused ferrogabbro with different water contents added to the charge show that generally high water activities could be achieved (crystallization of amphibole), independently of the bulk water content, even in a system with very low initial bulk water content (0.3 wt.%). Increasing water contents produce plagioclase richer in An, reduces the modal proportion of plagioclase in the crystallizing assemblage and extends the melt fraction. High melt fractions of >30 wt.% could only be observed in systems with high bulk water contents (>2 wt.%). This indicates that the migmatites were generated under water-rich conditions (probably water-saturated), since those migmatites, which are characterized as “in-situ” formations, show generally high amounts of leucosomes (>30 wt.%).     

Rutile R632 – A New Natural Reference Material for U‐Pb and Zr Determination

A new natural rutile reference material is presented, suitable for U‐Pb dating and Zr‐in‐rutile thermometry by microbeam methods. U‐Pb dating of rutile R632 using laser ablation ICP‐MS with both magnetic sector field and quadrupole instruments as well as isotope dilution‐thermal ionisation mass spectrometry yielded a concordia age of 496 ± 2 Ma. The high U content (> 300 μg g^?1) enabled measurement of high‐precision U‐Pb ages despite its young age. The sample was found to have a Zr content of 4294 ± 196 μg g^?1, which makes it an excellent complementary reference material for Zr‐in‐rutile thermometry. Individual rutile grains have homogeneous compositions of a number of other trace elements including V, Cr, Fe, Nb, Mo, Sn, Sb, Hf, Ta and W. This newly characterised material significantly expands the range of available rutile reference materials relevant for age and temperature determinations.     

Element signatures of subduction-zone fluids. An experimental study of the element partitioning (Dfluid/rock) of natural partly altered igneous rocks from the ODP drilling site 1,256

The trace element signatures of fluids were investigated by leaching experiments on natural samples of partly altered mafic igneous rocks recovered from the drilling site 1,256 of ODP Leg 206 on the Cocos plate (Central America). Experiments with ultrapure water were performed at 400 °C/0.4 GPa and 500 °C/0.7 GPa. Both fluids and residual solids were examined to obtain the partition coefficients (D^fluid/rock) of various trace elements. Element partition coefficients (D^fluid/rock) obtained at 500 °C/0.7 GPa are significantly lower compared to results obtained at 400 °C/0.4 GPa, which is in contrast to observations at higher pressures (2.2–6 GPa) and temperatures between 700 and 1,400 °C (Kessel et al. in Earth Planet Sci Lett 237: 873–892, 2005a; Spandler et al. in Chem Geol 239: 228–249, 2007). This finding may indicate a considerable pressure effect on the leaching processes and strongly divergent fluid–rock interactions in the upper part of a subduction zone at 0.4–0.7 GPa compared to deeper subduction areas with higher pressures. Furthermore, this may be interpreted as one of the earliest fractionation processes during the subduction of crustal material.     

Origin and age of ultramafic rocks and gabbros in the southern Puna of Argentina: an alleged Ordovician suture revisited

Ultramafic rocks and gabbros are exposed in the southern Puna (NW Argentina) in tectonic association with continental arc-related Ordovician (volcano) sedimentary successions and granitoids. The origin of this mafic rock suite has been debated for three decades as either representing an Ordovician terrane suture, primitive Ordovician arc-related rocks or relics of the pre-Ordovician basement in tectonic contact with the Ordovician retro-arc basin successions. We present the first U–Pb ages of primary and inherited zircon from gabbros of this mafic–ultramafic assemblage. LA-ICP-MS analyses on cores and rims of these zircon grains yielded a concordia age of 543.4 ± 7.2 Ma for the gabbroic rocks. Other analysed zircons have Mesoproterozoic, and Early Ediacaran core and rim ages indicating that the magmas also assimilated Meso- and Neoproterozoic crustal material prior to final crystallization. The mafic rocks witnessed higher metamorphic grade than associated Ordovician rocks, which are unmetamorphosed or only affected by anchimetamorphism. The gabbros are mostly tholeiitic and enriched in Zr, Th, as well as other incompatible elements and have εNd _t=540Ma ranging from 1.3 to 7.4 with most of the values between 5 and 7. ¹⁴⁷Sm/¹⁴⁴Nd ratios show evidence of weak crustal contamination. The mafic rocks do not reveal any affinity to mid-ocean ridge basalts in their geochemistry but point instead to an emplacement in an active plate margin arc environment. Chromites from ultramafic rocks show typical Ti, Al, Cr#, Fe³⁺ abundances found in magmatic arc rocks. The formation of the gabbros and the associated ultramafic rocks in the southern Argentine Puna is related to the evolution of the margin of the Pampia terrane, including the Puncoviscana basin, during the Late Neoproterozoic and earliest Cambrian. In contrast to previous interpretations, the rocks predate the Ordovician evolution of the Central proto-Andean active margin. Consequently, interpretations assuming these rocks to represent an oceanic terrane suture of Ordovician age have to be dismissed as much as all palaeotectonic models that define Ordovician terranes in the Central Andes based on assumption that the ultramafic rocks and gabbros exposed in the southern Puna mark plate boundaries.     

Neoarchean high-pressure margarite–phengitic muscovite–chlorite corona mantled corundum in quartz-free high-Mg,Al phlogopite–chlorite schists from the Bundelkhand craton,north central India

In quartz-free Fe, Na-poor and high-Mg, Al schists from the Bundelkhand craton in north central India, corundum porphyroblasts in finely interleaved phlogopite–chlorite aggregates with rare clinozoisite are mantled by fine-grained (<3 μm) intergrowths of outer collars (>200 μm wide) of phengitic-muscovite and chlorite (phlogopite + corundum + H₂O → phengitic-muscovite + chlorite), and <100 μm wide inner collars of margarite–muscovite (corundum + clinozoisite + phengitic muscovite → margarite + muscovite + H₂O). Wide-beam electron probe microanalyses indicate Mg in the bi-layered corona increases from corundum outwards, with a complementary decrease in Al and K. Si and Ca increase and then decrease to matrix values. The sharp chemical gradients across the highly structured bi-layered corona are inferred to suggest that the corona-forming reactions were promoted by local grain-boundary-controlled thermodynamic instability as opposed to element transport by advective diffusion. The P–T convergence of KMASH reactions and NCKMASH pseudosection phase relations computed using micro-domain compositions indicate the chlorite–phengitic muscovite outer collar formed at 18–20 kbar and ca. 630°C. The NCKMASH margarite–muscovite inner collar yielded lower metamorphic P–T conditions of 11 ± 3 kbar, ca. 630°C. U–Th–Pb chemical dating of metamorphic monazite and LA-ICPMS U–Pb isotope dating of re-equilibrated zircon yield ca. 2.78 Ga ages, which are interpreted to date corona formation and Neoarchean high-P metamorphism in the Bundelkhand craton, hitherto unknown in the Indian Precambrian. (220)     

Fluid venting and seepage at accretionary ridges: the Four Way Closure Ridge offshore SW Taiwan

Within the accretionary prism offshore SW Taiwan, widespread gas hydrate accumulations are postulated to occur based on the presence of a bottom simulating reflection. Methane seepage, however, is also widespread at accretionary ridges offshore SW Taiwan and may indicate a significant loss of methane bypassing the gas hydrate system. Four Way Closure Ridge, located in 1,500 m water depth, is an anticlinal ridge that would constitute an ideal trap for methane and consequently represents a site with good potential for gas hydrate accumulations. The analysis of high-resolution bathymetry, deep-towed sidescan sonar imagery, high-resolution seismic profiling and towed video observations of the seafloor shows that Four Way Closure Ridge is and has been a site of intensive methane seepage. Continuous seepage is mainly evidenced by large accumulations of authigenic carbonate precipitates, which appear to be controlled by the creation of fluid pathways through faulting. Consequently, Four Way Closure Ridge is not a closed system in terms of fluid migration and seepage. A conceptual model of the evolution of gas hydrates and seepage at accretionary ridges suggests that seepage is common and may be a standard feature during the geological development of ridges in accretionary prisms. The observation of seafloor seepage alone is therefore not a reliable indicator of exploitable gas hydrate accumulations at depth.     

Development and mass movement processes of the north-eastern Storegga Slide

The Storegga Slide, which occurred ～8100 years ago, is one of the world's largest and best studied exposed submarine landslides. In this study we use novel geomorphometric techniques to constrain the submarine mass movements that have shaped the north-eastern Storegga Slide, understand the link between different forms of failure, and propose a revised development model for this region. According to this model, the north-eastern part of the Storegga Slide has developed in four major events. The first event (event 1) was triggered in water depths of 1500–2000 m. In this event, the surface sediments were removed by debris flows and turbidity currents, and deposited in the Norwegian Sea Basin. Loading of the seabed by sediments mobilised by the debris flows and turbidity currents resulted in the development of an evacuation structure. Loss of support associated with this evacuation structure, reactivation of old headwalls and seismic loading activated spreading in the failure surface of event 1 up to the main headwall (event 2). In some areas, spreading blocks have undergone high displacement and remoulding. Parts of the spreading morphology and the underlying sediment have been deformed or removed by numerous debris flows and turbidity currents (event 3). We suggest that the higher displacement and remoulding of the spreading blocks, and their removal by debris flows and turbidity currents, was influenced by increased pore pressures, possibly due to gas hydrate dissolution/dissociation or by lateral variability in the deposition of contourite drifts in palaoeslide scars. The fourth event entailed a large, blocky debris flow that caused localised compression and transpressive shearing in the southern part of the spreading area.     

Experimental constraints on storage conditions in the chemically zoned phonolitic magma chamber of the Laacher See volcano

Phase relations of three samples of the Laacher See Tephra (LST) have been determined experimentally as a function of temperature (760 to 880 °C), pressure (200, 300 and 400 MPa), water content of the melt and oxygen fugacity (ƒO₂). The crystallization experiments were carried out at ƒO₂=NNO buffer and at NNO=+ 2.3 log units. The melt water contents varied between 6 and more than 8 wt% H₂O, corresponding to water-undersaturated and water saturated conditions respectively. The synthetic products are compared to the natural phases to constrain pre-eruptive conditions in the Laacher See magma chamber. The major phases occurring in the LST have been reproduced. The stability of hauyne is favoured at high ƒO₂ (≈NNO + 2.3). The CaO contents in melt and plagioclase synthesized under water-saturated conditions are significantly higher than in the natural phases, implying that most of the differentiation of the phonolites took place under water-undersaturated conditions. However, this does not exclude the presence of a S-, Cl- and CO₂-rich fluid phase in the upper parts of the magma chamber. The phase relationships and the TiO₂ contents of melts show that the temperature was lower than 760 °C in the upper part of the magma column (probably down to 720 °C in the most differentiated levels) and that temperatures above 840–860 °C prevailed in the lower part. The variation of the X _Mg of ferromagnesian minerals observed in both natural and experimental phases reflects the strong variations in ƒO₂ in the lower magma chamber just prior to eruption (probably variation of about 2 log units). The most probable explanation for these ƒO₂ variations is the injection of an oxidized alkali-rich magma, containing Mg-rich phenocrysts, at the base of a chemically zoned and more reduced magma column prior to eruption. Although the amount of injected magma may not have been very important, it was sufficient to change the ƒO₂ conditions locally, explaining the heterogeneous X _Mg of ferromagnesian minerals and the formation of hauyne at the base of the chamber. Received: 30 May 2000 / Accepted: 12 August 2000     

Fractionation of the noble metals by physical processes

During partial melting in the earth’s mantle, the noble metals become fractionated. Os, Ir, Ru, and Rh tend to remain in the mantle residue whereas Pt, Pd, and Re behave mildly incompatible and are sequestered to the silicate melt. There is consensus that sulfide plays a role in the fractionation process; the major noble metal repository in the mantle is sulfide, and most primitive mantle melts are sulfide-saturated when they leave their mantle sources. However, with sulfide–silicate partitioning, the fractionation cannot be modeled properly. All sulfide–silicate partition coefficients are so extremely high that a silicate melt segregating from a mantle source with residual sulfide should be largely platinum-group elements free. We offer a physical alternative to sulfide–silicate chemical partitioning and provide a mechanism of generating a noble metal-rich melt from a sulfide-saturated source: Because sulfide is at least partially molten at asthenospheric temperature, it will behave physically incompatible during melt segregation, and a silicate melt segregating from a mantle residue will entrain molten residual sulfide in suspension and incorporate it in the basaltic pool melt. The noble metal abundances of a basalt then become independent of sulfide–silicate chemical partitioning. They reflect the noble metal abundances in the drained sulfide fraction as well as the total amount of sulfide entrained. Contrary to convention, we suggest that a fertile, sulfide-rich mantle source has more potential to generate a noble metal-enriched basaltic melt than a refractory mantle source depleted by previous partial melting events.     

Microstructurally controlled trace element (Zr,U–Pb) concentrations in metamorphic rutile: An example from the amphibolites of the Bergen Arcs

As a common constituent of metamorphic assemblages, rutile provides constraints on the timing and conditions of rock transformation at high resolution. However, very little is known about the links between trace element mobility and rutile microstructures that result from synmetamorphic deformation. To address this issue, here we combine in situ LA-ICP-MS and sensitive high-resolution ion microprobe trace element data with electron back-scatter diffraction microstructural analyses to investigate the links between rutile lattice distortions and Zr and U–Pb systematics. Furthermore, we apply this integrated approach to constrain further the temperature and timing of amphibolite facies metamorphism and deformation in the Bergen Arcs of southwestern Norway. In outcrop, the formation of porphyroblastic rutile in dynamically hydrated leucocratic domains of otherwise rutile-poor statically hydrated amphibolite provides key contextual information on both the ambient conditions of hydration and deformation and the composition of the reactive fluid. Rutile in amphibolite recorded ambient metamorphic temperatures of ~590–730°C during static hydration of the granulitic precursor. By contrast, rutile from leucocratic domains in the directly adjacent shear zone indicates that deformation was accompanied by a localized increase in temperature. These higher temperatures are recorded in strain-free rutile (~600–860°C) and by Zr concentration measurements on low-angle boundaries and shear bands (620–820°C). In addition, we also observe slight depletions of Zr and U along rutile low-angle boundaries relative to strain-free areas in deformed grains from the shear zone. This indicates that crystal–plastic deformation facilitated the compositional re-equilibration of rutile upon cooling to slightly below the peak temperature of deformation. Cessation of deformation at mid-crustal conditions near ~600°C is recorded by late stage growth of small (<150 µm) rutile in the high-strain zones. U–Pb age data obtained from the strain-free and distorted rutile grains cluster in distinct populations of 437.4 ± 2.7 Ma and c. 405–410 Ma, respectively. These different ages are interpreted to reflect the difference in closure for thermally induced Pb diffusion between undeformed and deformed rutile during post-deformation exhumation and cooling. Thus, our results provide a reconstruction of the thermochronological history of the amphibolite facies rocks of the Lindås Nappe and highlight the importance of integration of microstructural data during application of thermometers and geochronometers.