Abundance Gradients in the Outer Galactic Disk

Radial abundance gradients of the element ratios O/H, Ne/H, S/H, and Ar/H are determined for a sample of disk planetary nebulae, emphasizing the behaviour of the gradients at large galactocentric distances. This revised version was published online in July 2006 with corrections to the Cover Date.     

Die stratiforme Sulfidlagerstätte Walchen,Steiermark, Österreich: Geochemie und Genese

Zusammenfassung Die Neubearbeitung derstratiformen Sulfidlagerstätte Walchen bei Öblarn, Steiermark, offen-bart eine eisenbetonte submarin-exhalative Metallkonzentration in einem vulkano-sedimentären Rahmen. Dieser liegt heute in Form metamorpher Gesteine der untersten Grünschieferfazies vor. Mineralchemische Untersuchungen zeigen, daß die ehemalige intensivste metamorphe Überprägung der Lagerstätte im Bereich von 450°–500°C oberhalb 4 kb stattgefunden hat. Metavulkanite, vertreten durch Grünschiefer, lassen alkalibasaltische Affinität erkennen. Die vulkano-tektonische Position der Lagerstätte ist in einem intrakontinentalen Riftsystem zu sehen.

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The stratiform sulphide deposit at walchen, styria, austria: Geochemistry and genesis

Summary The Walchen deposit consists of a 1–2 m thick layer of massive to disseminated pyrite-pyrrhotite-chalcopyrite ore with an average grade of 1% Cu. It has been mined intermittently in the past. The ore horizon occurs within sericitic and quartzitic phyllites which carry intercalations with significant carbonate, garnet and graphite contents. The succession is of lower Paleozoic age and forms part of the Grauwackenzone, a volcano-sedimentary unit which separates the Central Alps from the Northern Calcareous Alps.The precursor rocks of the ore environment have been pelites and sandstones; greenschists occur in the hanging wall of the mineralization. Major and trace element analyses of greenschists reveal them as low-grade metamorphic equivalents of continental alkali basalts. Hydrothermal systems generated by volcanic activity were responsible for deposition of stratiform sulphides. The predominance of clastic sediments and the absence of stringer zones point towards a shallow depositional basin.Microprobe analyses of garnets from the ore environment reveal an increase in spessartine contents from 7 mol% in phyllites to 20 mol% in the vicinity of the ore horizon. Similar data have been reported from other stratabound base metal deposits (Broken Hill, N.S.W.; Kreuzeck Mountains, Austria; Gamsberg, South Africa); the manganese concentrations represent fossil manganese haloes.Pyrite carries minor Ni and Co (up to 0.03, respectively 0.3%), pyrrhotite averages 0.8% Ni and 0.1% Co, Fe-contents of sphalerite vary from 6.41–9.33%; Cd, In and Mn have not been recorded.Garnet-biotite pairs suggest maximum metamorphic temperatures of 450°–500°C: pressures of 4 to 5 kb have been estimated. The Walchen deposit is interpreted as the product of submarine exhalative processes in an incipient rift. It was affected by prograde metamorphism during the Variscan orogeny, and by retrograde affects during a later event. Isochemical metamorphism resulted in the preservation of a primary manganese halo.

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Mit 6 Abbildungen     

Carbon isotopic fractionation between CO2 vapour,silicate and carbonate melts: an experimental study to 30 kbar

The carbon isotopic fractionation between CO₂ vapour and sodamelilite (NaCaAlSi₂O₇) melt over a range of pressures and temperatures has been investigated using solid-media piston-cylinder high pressure apparatus. Ag₂C₂O₄ was the source of CO₂ and experimental oxygen fugacity was buffered at hematite-magnetite by the double capsule technique. The abundance and isotopic composition of carbon dissolved in sodamelilite (SM) glass were determined by stepped heating and the ¹³C of coexisting vapour was determined directly by capsule piercing. CO₂ solubility in SM displays a complex behavior with temperature. At pressures up to 10 kbars CO₂ dissolves in SM to form carbonate ion complexes and the solubility data suggest slight negative temperature dependence. Above 20 kbars CO₂ reacts with SM to form immiscible Na-rich silicate and Ca-rich carbonate melts and CO₂ solubility in Na-enriched silicate melt rises with increasing temperature above the liquidus. Measured values for carbon isotopic fractionation between CO₂ vapour and carbonate ions dissoived in sodamelilite melt at 1200°–1400° C and 5–30 kbars average 2.4±0.2, favouring¹³C enrichment in CO₂ vapour. The results are maxima and are independent of pressure and temperature. Similar values of 2 are obtained for the carbon isotopic fractionation between CO₂ vapour and carbonate melts at 1300°–1400° C and 20–30 kbars.     

Lithologische Studien und zyklische Sedimentation in der helvetischen Zone der Schweizeralpen

Ohne Zusammenfassung     

Co-diagenesis of iron and phosphorus in hydrothermal sediments from the southern East Pacific Rise: Implications for the evaluation of paleoseawater phosphate concentrations

We present a detailed study of the co-diagenesis of Fe and P in hydrothermal plume fallout sediments from ∼19°S on the southern East Pacific Rise. Three distal sediment cores from 340-1130 km from the ridge crest, collected during DSDP Leg 92, were analysed for solid phase Fe and P associations using sequential chemical extraction techniques. The sediments at all sites are enriched in hydrothermal Fe (oxyhydr)oxides, but during diagenesis a large proportion of the primary ferrihydrite precipitates are transformed to the more stable mineral form of goethite and to a lesser extent to clay minerals, resulting in the release to solution of scavenged P. However, a significant proportion of this P is retained within the sediment, by incorporation into secondary goethite, by precipitation as authigenic apatite, and by readsorption to Fe (oxyhydr)oxides. Molar P/Fe ratios for these sediments are significantly lower than those measured in plume particles from more northern localities along the southern East Pacific Rise, and show a distinct downcore decrease to a depth of ∼12 m. Molar P/Fe ratios are then relatively constant to a depth of ∼35 m. The Fe and P speciation data indicate that diagenetic modification of the sediments is largely complete by a depth of 2.5 m, and thus depth trends in molar P/Fe ratios can not solely be explained by losses of P from the sediment by diffusion to the overlying water column during early diagenesis. Instead, these sediments are likely recording changes in dissolved P concentrations off the SEPR, possibly as a result of redistribution of nutrients in response to changes in oceanic circulation over the last 10 million years. Furthermore, the relatively low molar P/Fe ratios observed throughout these sediments are not necessarily solely due to losses of scavenged P by diffusion to the overlying water column during diagenesis, but may also reflect post-depositional oxidation of pyrite originating from the volatile-rich vents of the southern East Pacific Rise. This study suggests that the molar P/Fe ratio of oxic Fe-rich sediments may serve as a proxy of relative changes in paleoseawater phosphate concentrations, particularly if Fe sulfide minerals are not an important component during transport and deposition.