Geomagnetic Pc3 Pulsations During the Total Solar Eclipse on Aug 11, 1999

The solar eclipse on August 11, 1999, observed in the region covered by many geomagnetic observatories, has offered a unique opportunity to look for an effect of the eclipse on geomagnetic pulsations. The pulsation activity digital data have been taken from Budkov Observatory in the Czech Republic (in the X component only), from observatories in Germany (Niemegk, Fürstenfeldbruck, Bad Bergzabern), in Hungary (Nagycenk), and for comparison in South Africa (Hermanus, conjugate-point station), and in Finland (Sodankylä, far from the eclipse zone). At all these stations the field in all three component has been recorded. The pulsation amplitudes in the X component exhibit a long-term minimum near the time of the eclipse. Spectral analysis of selected short intervals confirmed this decrease and also revealed a decrease of the average pulsation period during the eclipse. Such a change in the amplitude or in the period was not observed outside of the eclipse interval or in other days. Investigation in some narrower frequency bands showed that the maximal decrease occurred in the 15–20 s band. All these changes can be found in records from all the stations near the eclipse totality belt, also in records at the conjugate-point station, where no eclipse occurred. No signature has been found in records at the station situated far from the eclipse zone.     

Special Contributions: Pictorial Series of the Manifestations of the Dynamics of the Earth: 5. Kamchatka,Its Early Cartography and Recent Climate Changes

Studia Geophysica et Geodaetica -     

A consistent derivation of the wave-energy equation from basic hydrodynamic principles

Based on a decomposition of the velocity into mean flow, turbulent and wave components, momentum and hereafter a wave-energy equation is derived. It contains a turbulent energy dissipation term which is closed by applying a wave-related mixing length model and linear wave theory solutions. This closure produces a non-linear turbulent wave-energy dissipation including the wave energy in a 5/2 power law. The theory is able to predict correctly the shape of deep-water wave spectra according to Phillips' similarity law.Responsible Editor: Hans Burchard     

Diamond formation and source carbonation: mineral associations in diamonds from Namibia

Mineral inclusions in diamonds from Namibia document a range of mantle sources, including eclogitic, websteritic and peridotitic parageneses. Based on unusual textural features a group of inclusions showing websteritic, peridotitic and transitional chemical features is assigned to an 'undetermined suite' (12% of the studied diamonds). The mutual characteristic of this group is the occurrence of lamellar intergrowths of clinopyroxene and orthopyroxene. In addition, the 'undetermined suite' is associated with a number of uncommon phases: in one diamond MgCO₃ is enclosed by clinopyroxene. Other minerals that form touching inclusions with the pyroxene lamellae are (1) a SiO₂ phase observed in three diamonds, together with CaCO₃ in one of them, (2) phlogopite and a Cr-rich 'titanate' (probably lindsleyite). The inclusions document a metamorphic path of decreasing pressures and temperatures after entrapment in diamond. First, homogeneous low-Ca clinopyroxenes were entrapped at high temperatures. They subsequently exsolved orthopyroxene and probably also SiO₂ (coesite) on cooling along a P,T trajectory that did not allow garnet to be exsolved as well. Phlogopite, carbonates and LIMA phases are the result of overprint of a peridotitic source rock by a carbon-rich agent. The resulting unusual, olivine-free mineral association and the host diamonds are interpreted as products of extensive carbonation of the peridotite.     

A Sr isotope study on fluorite and siderite from post-orogenic mineral veins in the eastern Harz Mountains,Germany

Rb–Sr isotope data for siderite and fluorite from sediment-hosted epithermal mineral veins in the eastern Harz Mountains (Germany) are presented. Several fluorite and siderite-bearing paragenetic stages have been proposed for these veins, with the most important mineralization being related to a quartz–sulfide and a subsequent calcite–fluorite–quartz stage, which occurred at 226±1 and 209±2 Ma, respectively. Our Rb–Sr data do not permit the identification of distinct generations of siderite and fluorite, but rather reveal straight internal mixing relations, reflecting mixing of fluids or differential fluid–rock interaction processes. This indicates merely two significant phases of mineral deposition related to the quartz–sulfide and calcite–fluorite–quartz stages. It is shown that the Paleozoic sedimentary host rocks of the veins are the most likely source for the siderite Sr, whereas fluorite displays a two-component mixture between sedimentary Sr and radiogenic Sr derived from locally occurring Permian metavolcanic rocks. Editorial handling: B. Lehmann     

Geochemistry and mineralogy of Platinum-group elements in the Ransko gabbro–peridotite massif,Bohemian Massif (Czech Republic)

The Ransko gabbro-peridotite massif in Eastern Bohemia is a strongly differentiated intrusive complex of Lower Cambrian age. The complex hosts low grade Ni-Cu ores mainly developed close to the contact of olivine-rich rocks with gabbros, in troctolites and, to a much lesser extent, in both pyroxene and olivine gabbros and plagioclase-rich peridotites. The ore zone is characterized by strong serpentinization and uralitization. The total Ni + Cu locally reaches up to 4 wt%. Anomalous concentrations of platinum-group elements (PGE's) (maximum 532 ppb Pd, 182 ppb Pt, 53 ppb Rh, 15 ppb Ru, 41 ppb Ir) were detected in samples of Cu-Ni and Ni-Cu ores (maximum 2.63 wt% Ni and 2.31 wt% Cu) from the Jezírka orebody. The main ore paragenesis includes pyrrhotite, pentlandite, chalcopyrite, cubanite, pyrite, magnetite, mackinawite, valleriite, ilmenite and sphalerite. During this work, michenerite, froodite, sperrylite, gold, native bismuth, altaite, tsumoite, hessite, an unnamed Bi-Ni telluride, cobaltite-gersdorffite and galena were newly identified. The host rocks originated through partial melting of a slightly depleted mantle source with noble metals scavenged from this primitive magma prior to the development of these rocks.     

Groundwater and volcanoes: examples from the Azores archipelago

Groundwater at the Azores archipelago is a strategic resource for the freshwater supply. Freshwater, mineral and thermal water discharges occur in the archipelago, and especially at the Fogo and Furnas volcanoes (São Miguel). These discharges provide data for case studies of groundwater chemistry from volcanic monitoring due to the stable composition of the sampled waters. The mineral and thermal discharges are mainly of sodium bicarbonate types and present a large range of temperatures, from cold springs to waters at about 90 °C. Some boiling discharges have a sulfate-dominated composition, suggesting a steam-heating mechanism. Geochemical studies on these mineral and thermal waters began in the 19th century. Data gathered since these earlier studies provide a baseline for pH, temperature, CO₂ and major-element composition. Weekly measurements of pH and temperature also denote a rather stable behavior.     

GIS-based determination of the mean long-term groundwater recharge in Lower Saxony

This paper presents the findings of a collaborative research project of the Geological Survey of Lower Saxony (NLfB) and the Programme Group Systems Analysis and Technology Evaluation (STE) of Research Centre Jülich on the GIS-based determination of the mean long-term groundwater recharge in Lower Saxony using high-resolution digital data (Dörhöfer and others 2001). The model calculations were performed on the basis of the water-balance model GROWA (Kunkel and Wendland 2002) with a spatial resolution of 100x100 m². The accuracy of the calculated groundwater recharge values for the period 1961–1990 was verified on the basis of data from gauging stations and displayed a good agreement between observed runoff values and model results.     

Sequential extraction procedure in columns. Part 1: Development and description of a new method

A sequential extraction procedure was carried out in columns using reagents that are known to be reliable from batch tests. The intention was to distinguish between different chemical forms of iron and heavy metals in samples from reduced porous aquifers, which demands anaerobic conditions for the extraction procedure and the determination of small amounts of reactive mineral phases in a quartz dominated sediment system. By means of the developed method, anaerobic conditions can be guaranteed in the columns, which could not be realized to full satisfaction in batch tests that were carried out in a glove box. In order to distinguish between the fractions that were water soluble, exchangeable, bound to carbonates and bound to hydroxides, different reagents were pumped through the sediments and sampled after passage of the columns. Sediment samples of 10 kg each were investigated in this way. The extraction steps were known to be complete when analyses revealed that no further major and trace elements were leached out of the columns. This approach enabled well-adjusted amounts of reagents to be used. By means of the sequential extraction procedure in columns the composition of even small amounts of reactive mineral phases can be determined successfully, which contributes to a deeper understanding of the hydrogeochemical processes in aquifers. In batch tests this accuracy cannot be reached because of the surplus of the extraction solution in relation to the amount of sediment (higher solution-sediment ratio). Furthermore, larger samples are much more representative of the composition of the aquifers than smaller ones and the heterogeneity of the sediment does not limit the accuracy of the results as much as in batch tests. In addition, the technique of flushing sediment in a column is much more typical for the situation in an aquifer than suspending a few grams of a sample in the extracting reagents in batch extraction tests. In order to demonstrate the methodical improvements and field applications, the newly developed method was used to investigate the changing binding forms and mobility of iron and trace metals in samples from a lignite overburden dump, which are influenced by pyrite oxidation processes (acidification) followed by the addition of crushed limestone (neutralization) (see "Sequential extraction procedure in columns. Part 2: Application of a new method").