The Petrology and Genesis of Silicic Magmas in the Kermadec Arc

<p>Recent work has shown that silicic volcanism can be abundant in intra-oceanic subduction settings, and is often associated with large explosive caldera-forming eruptions. Several major petrogenetic questions arise over the origin and eruption of large amounts of silicic magma at these relatively simple subduction settings. This study has investigated the geochemistry of pyroclasts collected from four volcanoes along the Kermadec arc, a young (<2 Myr) oceanic subduction zone in the southwest Pacific. Raoul, Macauley and a newly discovered volcano (here informally named 'New volcano') in the northern Kermadec arc, and Healy volcano in the southern Kermadec arc have all erupted dacitic to rhyolitic pumice within the last 10 kyr. For Raoul, New volcano and Healy, whole rock major element compositions fall with a limited compositional range. In contrast, pumice dredged from around Macauley caldera covers a wide compositional range indicating that there have been multiple silicic eruptions, not just the Sandy Bay Tephra exposed on Macauley Island. Distinctive crystal populations in both pumice samples and plutonic xenoliths suggest that many of the crystals did not grow in the evolved magmas, but were mixed in from other sources including gabbros and tonalites. Such open system mixing is ubiquitous in magmas from the four Kermadec volcanoes studied here. Silicic magmas, co-eruptive mafic enclaves and previously erupted basalts show sub-parallel REE patterns, and crystal composition and zonation suggests that mafic and silicic magmas have a strong genetic affiliation. Examination of whole rock, glass and mineral chemistry reveals that evolved magmas can be generated at each volcano through 60-75% crystal fractionation of a basaltic parent. These findings are not consistent with silicic magma generation via crustal anatexis, as previously suggested for the Kermadec arc. Although crystallisation is the dominant process driving melt evolution in the Kermadec volcanoes, the magmatic systems are open to contributions from both newly arriving melts and wholly crystalline plutonic bodies. Such processes occur in variable proportions between magma batches, and are largely reflected by small scale chemical variations between eruption units. Larger scale chemical trends reflect the position of the volcanoes along the arc, which in turn may reflect structural changes in the subduction zone and variations in sediment influx.</p>

The Petrology and Genesis of Silicic Magmas in the Kermadec Arc

<p>Recent work has shown that silicic volcanism can be abundant in intra-oceanic subduction settings, and is often associated with large explosive caldera-forming eruptions. Several major petrogenetic questions arise over the origin and eruption of large amounts of silicic magma at these relatively simple subduction settings. This study has investigated the geochemistry of pyroclasts collected from four volcanoes along the Kermadec arc, a young (<2 Myr) oceanic subduction zone in the southwest Pacific. Raoul, Macauley and a newly discovered volcano (here informally named 'New volcano') in the northern Kermadec arc, and Healy volcano in the southern Kermadec arc have all erupted dacitic to rhyolitic pumice within the last 10 kyr. For Raoul, New volcano and Healy, whole rock major element compositions fall with a limited compositional range. In contrast, pumice dredged from around Macauley caldera covers a wide compositional range indicating that there have been multiple silicic eruptions, not just the Sandy Bay Tephra exposed on Macauley Island. Distinctive crystal populations in both pumice samples and plutonic xenoliths suggest that many of the crystals did not grow in the evolved magmas, but were mixed in from other sources including gabbros and tonalites. Such open system mixing is ubiquitous in magmas from the four Kermadec volcanoes studied here. Silicic magmas, co-eruptive mafic enclaves and previously erupted basalts show sub-parallel REE patterns, and crystal composition and zonation suggests that mafic and silicic magmas have a strong genetic affiliation. Examination of whole rock, glass and mineral chemistry reveals that evolved magmas can be generated at each volcano through 60-75% crystal fractionation of a basaltic parent. These findings are not consistent with silicic magma generation via crustal anatexis, as previously suggested for the Kermadec arc. Although crystallisation is the dominant process driving melt evolution in the Kermadec volcanoes, the magmatic systems are open to contributions from both newly arriving melts and wholly crystalline plutonic bodies. Such processes occur in variable proportions between magma batches, and are largely reflected by small scale chemical variations between eruption units. Larger scale chemical trends reflect the position of the volcanoes along the arc, which in turn may reflect structural changes in the subduction zone and variations in sediment influx.</p>

Effect of Mn Substitution Fe on the Formability and Magnetic Properties of Amorphous Fe88Zr8B4 Alloy

Elemental substitution is commonly used to improve the formability of metallic glasses and the properties of amorphous alloys over a wide compositional range. Therefore, it is essential to investigate the influence of element content change on the formability as well as magnetic and other properties. The purpose is to achieve tailorable properties in these alloys with enhanced glass forming ability. In this work, the glass-forming ability (GFA) and magnetic properties of the minor Mn-substituted Fe88Zr8B4 amorphous alloy were investigated. The addition of Mn improving the amorphous forming ability of the alloy. With the addition of Mn, the magnetic transition temperature, saturation magnetization and the magnetic entropy changes (−ΔSm) peaks decreased simultaneously, which is possibly caused by the antiferromagnetic coupling between Fe and Mn atoms. The dependence of −ΔSmpeak on Tc displays a positive correlation compared to the −ΔSmpeak- Tc−2/3 relationship proposed by Belo et al.

Electronic properties of phases in the quasi-binary Bi2Se3-Bi2S3 system.

We explored the properties of the quasi-binary Bi2Se3-Bi2S3 system over a wide compositional range. X-ray diffraction analysis demonstrates that rhombohedral crystals can be synthesized within the solid solution interval 0-22...

Crystal Chemistry of an Erythrite-Köttigite Solid Solution (Co3–xZnx) (AsO4)2·8H2O

A wide compositional range, covering about 90% of an expected erythrite-köttigite substitutional solid solution with extreme compositions of (Co2.84Mg0.14Zn0.02) (AsO4)2·8H2O and (Zn2.74Co0.27) (AsO4)2·8H2O, was revealed in a suite of samples from a polymetallic ore deposit in Miedzianka, SW Poland. Members of the solid solution series were examined by means of Electron Probe Microanalysis (EPMA), Scanning Electron Microscopy (SEM)/Energy-Dispersive Spectrometer (EDS), X-ray single-crystal and powder diffraction, and Raman spectroscopy. Metal cations were randomly distributed between two special octahedral sites in the erythrite–köttigite structure. In response to Co ↔ Zn substitutions, small but significant changes in bond distances (particularly in [AsO4] tetrahedra), rotation, and distortion of co-ordination polyhedra were observed. Two sub-series of dominant cationic substitutions (Co-Mg-Ni and Co-Fe-Zn) were noted within the arsenate series of vivianite-group minerals linked by erythrite. The paragenetic sequence erythrite → Zn-rich erythrite → Co-rich köttigite → köttigite reflects the evolution of the solution’s pH towards increased acidity and a relative increase in the concentration of Zn ions following precipitation of erythrite.

Clinopyroxene/Melt Trace Element Partitioning in Sodic Alkaline Magmas

Clinopyroxene is a key fractionating phase in alkaline magmatic systems, but its impact on metal enrichment processes, and the formation of REE + HFSE mineralisation in particular, is not well understood. To constrain the control of clinopyroxene on REE + HFSE behaviour in sodic (per)alkaline magmas, a series of internally heated pressure vessel experiments was performed to determine clinopyroxene–melt element partitioning systematics. Synthetic tephriphonolite to phonolite compositions were run H2O-saturated at 200 MPa, 650–825°C with oxygen fugacity buffered to log f O2 ≈ ΔFMQ + 1 or log f O2 ≈ ΔFMQ +5. Clinopyroxene–glass pairs from basanitic to phonolitic fall deposits from Tenerife, Canary Islands, were also measured to complement our experimentally-derived data set. The REE partition coefficients are 0·3–53, typically 2–6, with minima for high-aegirine clinopyroxene. Diopside-rich clinopyroxene (Aeg5–25) prefer the MREE and have high REE partition coefficients (DEu up to 53, DSm up to 47). As clinopyroxene becomes more Na- and less Ca-rich (Aeg25–50), REE incorporation becomes less favourable, and both the VIM1 and VIIIM2 sites expand (to 0·79 Å and 1·12 Å), increasing DLREE/DMREE. Above Aeg50 both M sites shrink slightly and HREE (VIri ≤ 0·9 Å ≈ Y) partition strongly onto the VIM1 site, consistent with a reduced charge penalty for REE3+ ↔ Fe3+ substitution. Our data, complemented with an extensive literature database, constrain an empirical model that predicts trace element partition coefficients between clinopyroxene and silicate melt using only mineral major element compositions, temperature and pressure as input. The model is calibrated for use over a wide compositional range and can be used to interrogate clinopyroxene from a variety of natural systems to determine the trace element concentrations in their source melts, or to forward model the trace element evolution of tholeiitic mafic to evolved peralkaline magmatic systems.

Mineralogical Study of the Advanced Argillic Alteration Zone at the Konos Hill Mo–Cu–Re–Au Porphyry Prospect, NE Greece

The Konos Hill prospect in NE Greece represents a telescoped Mo–Cu–Re–Au porphyry occurrence overprinted by deep-level high-sulfidation mineralization. Porphyry-style mineralization is exposed in the deeper parts of the system and comprises quartz stockwork veins hosted in subvolcanic intrusions of granodioritic composition. Ore minerals include pyrite, molybdenite, chalcopyrite, and rheniite. In the upper part of the system, intense hydrothermal alteration resulted in the formation of a silicified zone and the development of various advanced argillic alteration assemblages, which are spatially related to N–S, NNW–SSE, and E–W trending faults. More distal and downwards, advanced argillic alteration gradually evolves into phyllic assemblages dominated by quartz and sericite. Zunyite, along with various amounts of quartz, alunite, aluminum phosphate–sulfate minerals (APS), diaspore, kaolinite, and minor pyrophyllite, are the main minerals in the advanced argillic alteration. Mineral-chemical analyses reveal significant variance in the SiO2, F, and Cl content of zunyite. Alunite supergroup minerals display a wide compositional range corresponding to members of the alunite, beudantite, and plumbogummite subgroups. Diaspore displays an almost stoichiometric composition. Mineralization in the lithocap consists of pyrite, enargite, tetrahedrite/tennantite, and colusite. Bulk ore analyses of mineralized samples show a relative enrichment in elements such as Se, Mo, and Bi, which supports a genetic link between the studied lithocap and the underlying Konos Hill porphyry-style mineralization. The occurrence of advanced argillic alteration assemblages along the N–S, NNW–SSE, and E–W trending faults suggests that highly acidic hydrothermal fluids were ascending into the lithocap environment. Zunyite, along with diaspore, pyrophyllite, and Sr- and Rare Earth Elements-bearing APS minerals, mark the proximity of the hypogene advanced argillic alteration zone to the porphyry environment.

Brønsted acids in ionic liquids: how acidity depends on the liquid structure

Gutmann Acceptor Number (AN) values have been determined for Brønsted acid–ionic liquid mixtures, over a wide compositional range.

Preparation and Properties of PTFE-PMMA Core-Shell Nanoparticles and Nanocomposites

The preparation of polytetrafluoroethylene-poly(methyl methacrylate) (PTFE-PMMA) core-shell particles was described, featuring controlled size and narrow size distribution over a wide compositional range, through a seeded emulsion polymerization starting from a PTFE seed of 26 nanometers. Over the entire MMA/PTFE range, the particle size increases as the MMA/PTFE ratio increases. A very precise control over the particle size can be exerted by properly adjusting the ratio between the monomer and the PTFE seed. Particles in the 80–240 nm range can be prepared with uniformity indexes suited to build 2D and 3D colloidal crystals. These core-shell particles were employed to prepare nanocomposites with different compositions, through an annealing procedure at a temperature higher than the glass transition temperature of the shell forming polymer. A perfect dispersion of the PTFE particles within the PMMA matrix was obtained and optically transparent nanocomposites were prepared containing a very high PTFE amount.