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>

Impact of the Allowed Compositional Range of Additively Manufactured 316L Stainless Steel on Processability and Material Properties

This work aims to show the impact of the allowed chemical composition range of AISI 316L stainless steel on its processability in additive manufacturing and on the resulting part properties. ASTM A276 allows the chromium and nickel contents in 316L stainless steel to be set between 16 and 18 mass%, respectively, 10 and 14 mass%. Nevertheless, the allowed compositional range impacts the microstructure formation in additive manufacturing and thus the properties of the manufactured components. Therefore, this influence is analyzed using three different starting powders. Two starting powders are laboratory alloys, one containing the maximum allowed chromium content and the other one containing the maximum nickel content. The third material is a commercial powder with the chemical composition set in the middle ground of the allowed compositional range. The materials were processed by laser-based powder bed fusion (PBF-LB/M). The powder characteristics, the microstructure and defect formation, the corrosion resistance, and the mechanical properties were investigated as a function of the chemical composition of the powders used. As a main result, solid-state cracking could be observed in samples additively manufactured from the starting powder containing the maximum nickel content. This is related to a fully austenitic solidification, which occurs because of the low chromium to nickel equivalent ratio. These cracks reduce the corrosion resistance as well as the elongation at fracture of the additively manufactured material that possesses a low chromium to nickel equivalent ratio of 1.0. A limitation of the nickel equivalent of the 316L type steel is suggested for PBF-LB/M production. Based on the knowledge obtained, a more detailed specification of the chemical composition of the type 316L stainless steel is recommended so that this steel can be PBF-LB/M processed to defect-free components with the desired mechanical and chemical properties.

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...

A structure hierarchy for silicate minerals: chain, ribbon, and tube silicates

A structure hierarchy is developed for chain-, ribbon- and tube-silicate based on the connectedness of one-dimensional polymerisations of (TO4)n− tetrahedra, where T = Si4+ plus P5+, V5+, As5+, Al3+, Fe3+, B3+, Be2+, Zn2+ and Mg2+. Such polymerisations are described by a geometrical repeat unit (with ng tetrahedra) and a topological repeat unit (or graph) (with nt vertices). The connectivity of the tetrahedra (vertices) in the geometrical (topological) repeat units is denoted by the expression cTr (cVr) where c is the connectivity (degree) of the tetrahedron (vertex) and r is the number of tetrahedra (vertices) of connectivity (degree) c in the repeat unit. Thus cTr = 1Tr12Tr23Tr34Tr4 (cVr = 1Vr12Vr23Vr34Vr4) represents all possible connectivities (degrees) of tetrahedra (vertices) in the geometrical (topological) repeat units of such one-dimensional polymerisations. We may generate all possible cTr (cVr) expressions for chains (graphs) with tetrahedron (vertex) connectivities (degrees) c = 1 to 4 where r = 1 to n by sequentially increasing the values of c and r, and by ranking them accordingly. The silicate (sensu lato) units of chain-, ribbon- and tube-silicate minerals are identified and associated with the relevant cTr (cVr) symbols. Following description and association with the relevant cTr (cVr) symbols of the silicate units in all chain-, ribbon- and tube-silicate minerals, the minerals are arranged into decreasing O:T ratio from 3.0 to 2.5, an arrangement that reflects their increasing structural connectivity. Considering only the silicate component, the compositional range of the chain-, ribbon- and tube-silicate minerals strongly overlaps that of the sheet-silicate minerals. Of the chain-, ribbon- and tube-silicates and sheet silicates with the same O:T ratio, some have the same cVr symbols (vertex connectivities) but the tetrahedra link to each other in different ways and are topologically different. The abundance of chain-, ribbon- and tube-silicate minerals decreases as O:T decreases from 3.0 to 2.5 whereas the abundance of sheet-silicate minerals increases from O:T = 3.0 to 2.5 and decreases again to O:T = 2.0. Some of the chain-, ribbon- and tube-silicate minerals have more than one distinct silicate unit: (1) vinogradovite, revdite, lintisite (punkaruaivite) and charoite have mixed chains, ribbons and/or tubes; (2) veblenite, yuksporite, miserite and okenite have clusters or sheets in addition to chains, ribbons and tubes. It is apparent that some chain-ribbon-tube topologies are favoured over others as of the ~450 inosilicate minerals, ~375 correspond to only four topologically unique graphs, the other ~75 minerals correspond to ~46 topologically unique graphs.