Crustal motion and deformation in Greece from a decade of GPS measurements, 1993–2003

The Hellenic plate boundary region, located in the collision zone between the Nubian/Arabian and Eurasian lithospheric plates, is one of the seismo-tectonically most active areas of Europe. During the last 15 years, GPS measurements have been used to determine the crustal motion in the area of Greece with the aim to better understand the geodynamical processes of this region. An extended reoccupation network covering whole Greece has been measured periodically in numerous GPS campaigns since the late eighties, and a continuous GPS network has been operated in the region of the Ionian Sea since 1995. In this paper, we present a new detailed high-quality solution of continuous and campaign-type measurements acquired between 1993 and 2003. During the GPS processing, a special effort was made to obtain consistent results with highest possible accuracies and reliabilities. Data of 54 mainly European IGS and EUREF sites were included in the GPS processing in order to obtain results which are internally consistent with the European kinematic field and order to allow for a regional interpretation. After an overview of the results of the IGS/EUREF sites, the results from more than 80 stations in Greece are presented in terms of velocities, time series, trajectories and strain rates. Previous geodetic, geological and seismological findings are generally confirmed and substantially refined. New important results include the observation of deformation zones to the north and to the south of the North Aegean Trough and in the West Hellenic arc region, arc-parallel extension of about 19 mm/yr along the Hellenic arc, and compression between the Ionian islands and the Greek mainland. Due to continuous long-term observations of 4–8 years, it was possible to extract height changes from the GPS time series. In Greece, we observe a differential subsidence of the order of 2 mm/yr between the northern and central Ionian islands across the Kefalonia fault zone. The differential subsidence of the central Ionian islands with respect to the northwestern Greek mainland amounts to 4 mm/yr.     

Georadiochemical evidence to weathering of mining residues of the Mansfeld mining district,Germany

Mining heaps are used as archives for the investigation of weathering processes. Aim of this work was to investigate the different weathering behavior of heap materials derived from Kupferschiefer mining with respect to environmental hazard. For this purpose, Kupferschiefer and slag material of two heaps of different age were examined regarding to the radionuclide distribution and geochemical composition. By measuring of the local dose rate, performing digital autoradiography and gamma spectrometry the radiological load of the heaps and the heap materials was determined. The geochemical characterization of the samples was performed by XRF, ICP–OES and ICP–MS. The results show a clear higher radionuclide load of the younger slag heap. A depletion of chalcophile and lithophile elements in the older slag was determined. Apart from a homogeneous radionuclide distribution, considerable radionuclide enrichments in fossil fragments could be proven. The results reveal a different weathering behavior of slag material in comparison to the Kupferschiefer depending on the chemical binding of the elements on organic and inorganic species. Natural organic matter as well as apatite in Kupferschiefer act as retention barrier for some metals.     

Neue ZnS-Polytypen (9R, 12R und 21R) in mesozoischen Sedimenten NW-Deutschlands

Summary Argillaceous sediments of jurassic and lower cretaceous age in NW-Germany contain in several localities authigenous ZnS-polytypes. The crystals with a maximum height of 2 mm exhibit hexagonal-pyramidal and trigonal-pyramidal habit.With X-ray rotation and precession technique the following polytypes could be identified: Sphalerite (3 R = 3 C) 211, 411, 6H 9R, 12R, 15R and 21R.The 9 R-, 12 R- and 21 R-polytypes have not until now been described elsewhere.The structures of the new polytypes were determined as 9R=(21), 12R=(13) and 21R=(3112).Oriented intergrowths of R- and H-polytypes were frequently observed. From the intergrowth-phenomena arguments for the environmental conditions of formation can be deducted.[/p]     

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Ohne Zusammenfassung     

Quaternary geology of the Amazonian Lowland

The Quaternary history of the Amazon lowlands is characterized by deposition of sediments of Andean provenance and by the influences of changing sea levels. Areas well above the present water tables were not reached by Pleistocene high-water stages. These areas have been intensively weathered since the Tertiary, forming hard lateritic weathering horizons. These weathering horizons are best explained by the relatively constant, humid tropical climate throughout the Quaternary. In the western Amazonian Lowland, flood plains corresponding to the different Pleistocene sea-level heights were formed. During low sea level, erosion in the drainage areas increased and the water levels of the central Amazon River system were lowered. Valleys drowned and lakes formed in the lower reaches of rivers and creeks during high sea-level stages. These lakes (ria lakes) remained in the valleys with rivers having a low sediment load. Seismic profiling (3.5 kHz) in some of these lakes clearly showed deposits of the three last periods of Quaternary high sea-level stages.     

Flow fields in reflected waves at a sloped sea wall

Wave run-up, and flow visualization experiments were conducted with a 1:2 sloped sea wall model. The visualization experiments gave an overview of flow fields in reflected, non-breaking conditions. Maximum particle velocities were found to be significantly smaller than suggested in the literature. Downrush produced a fast sheet flow, extending down to the toe of the sea wall. This created a ‘reverse’ breaker during the retreat of the initially non-breaking wave, which explains the high-energy dissipation rates for non-breaking waves reported in the literature. Embankments may therefore be exposed to wave impact pressures in areas up to 1.18H₀ below MWL.     

Transition from eclogite to amphibolite-facies metamorphism in the Austroalpine Ulten Zone

Summary The Ulten Zone of the Austroalpine crystalline basement south-west of Meran (Italy) contains metapelitic schists and granoblastic paragneisses, leucocratic orthogneisses, migmatites (in both gneiss-lithologies), metabasites and ultramafic lenses. Metamorphic textures of the metapelitic schists and granoblastic paragneisses indicate two different metamorphic events, characterized by two mineral assemblages, which differ in mineral chemistry: (1) an eclogite facies mineral assemblage (M1) comprising Grt-Ky I-Bt. Ms-Kfs-PI-Qtz-Rt, and (2) an amphibolite facies mineral assemblage (M2) comprising Grt-KyII-Bt-Ms-PI-Qtz-Ilm±St. For the M1 event, pressures of at least 15kbar and temperatures of about 700°±50°C can be estimated. The later amphibolite facies overprint occurred at pressures of 6 to 8kbar and about 600°±50°C. The M1 and M2 assemblages belong to a continuous clockwise metamorphic evolution during the Variscan orogeny. Evidence for Alpine metamorphism can only be detected by sericite rims around kyanite and reset biotite ages. The migmatites, which contribute about 15–30vol.% of all rocks in the investigated area, were formed on the prograde path during the M1 event. Dissolution of H₂O in the melted part of the migmatites resulted in a CO₂dominated fluid, which was trapped in primary kyanite (M1) fluid inclusions. Secondary H₂O-rich fluid inclusions are found in quartz grains and may represent the fluid which enabled a pervasive equilibration during M2.

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Übergang von eklogit-zu amphibolitfazieller Matamorphose in der austroalpinen Ultenzone

Zusammenfassung Die Ulten Zone, ein Teil des ostalpinen kristallinen basements, südwestlich von Meran, wird aus Metapeliten and granoblastischen Paragneisen, leukokraten Orthogneisen, Migmatiten (in beiden Lithologien), Metabasiten and ultramafischen Linsen aufgebaut. Metamorphe Texturen der Metapelite und granoblastischen Paragneise lassen auf zwei verschiedene metamorphe Ereignisse schließen, die durch unterschiedliche Mineral-chemismen und Paragenesen charakterisiert sind: (1) eine eklogitfazielle Paragenese (M1), bestehend aus Grt-KyI-Bt-Ms-Kfs-P1-Qtz-Rt und (2) eine amphibolitfazielle Paragenese (M2), bestehend aus Grt-KyII-Bt-Ms-P1-Qtz-Ilm±St. Für M1 konnten Minimaldrucke von 15kbar und Temperaturen von 700°±50°C abgeleitet werden. Die spätere amphibolitfazielle Überprägung fand bei 6 bis 8kbar und 600°±50°C statt. M1 und M2 gehören einer kontinuierlichen Metamorphoseentwicklung während der variszischen Orogenese an.Die Migmatite, ungefähr 15–30vol.% der Gesteine im untersuchten Gebiet, wurden am prograden Pfad während des M1 Ereignisses gebildet. Aufgrund der höheren Löslichkeit von H₂0 in der Schmelze, blieb ein CO₂, reiches Fluid zurück, das im primären Kyanit (M1) eingeschlossen wurde. Wässrige Flüssigkeitseinschlüsse können in Quarzkörnern gefunden werden. Dieses Fluid ist wahrscheinlich für die Reequilibrierung zu amphibolitfaziellen Bedingungen verantwortlich.

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With 5 Figures     

The shoshonite porphyry Cu-Au association in the Goonumbla District,N.S.W., Australia

Summary The Goonumbla porphyry copper-gold deposit in N.S.W., Australia, is hosted by late Ordovician (439.2 ± 1.2 Ma)shoshonitic igneous rocks. In terms of their petrography, the rocks vary from andesitic to dacitic lavas and tuffs which are partly intruded by monzonite stocks; they are characterized by high and variable Al₂O₃ (13.4–19.9 wt%), very high K₂O values (up to 6.8 wt%), and high K₂O/Na₂O ratios (0.58–1.48), which are typical for the shoshonite association. The rocks also have enriched LILE concentrations (Ba up to 1200 ppm, Sr up to 1350 ppm), low HFSE (TiO₂ < 0.67 wt%, Zr < 125 ppm, Nb < 10 ppm, Hf < 3.4 ppm), and very low LREE (La < 22.4 ppm, Ce < 31 ppm), which are typical for potassic volcanic rocks formed in alate oceanic-arc setting.Mineral chemistry of selected magmatic mica and apatite phenocrysts from host rocks reveals relatively high SrO and BaO contents (micas: 0.15 wt% and up to 0.28 wt%, respectively; apatites: up to 0.28 wt% and 0.19 wt%, respectively) and very high halogen concentrations. Micas are characterized by up to 3.9 wt% F and 0.14 wt% Cl, whereas apatites have up to 3.6 wt% F and 0.68 wt% Cl. These very high halogen contents compared to those from barren intrusions imply that the shoshonitic magmatism was the source of mineralization.Copper-gold mineralization consists mainly of bornite, chalcopyrite, chalcocite and minor pyrite and tetrahedrite. Native gold occurs mainly as minute grains within silicates of the host rocks, and more rarely as fine inclusions in the sulphides. Mineralization is accompanied by wallrock alteration comprising a spatially restricted potassic type and a regional propylitic alteration type.Thus, the porphyry copper-gold deposit in the Goonumbla district can be viewed as an additional example of a worldwide association between potassic/shoshonitic magmatism and base- and precious-metal mineralization. More specifically, it appears to be the oldest recorded example of a shoshontie-associated porphyry Cu-Au deposit from a late oceanic-arc setting, a possible modern analogue being Ladolam at Lihir Island, Papua New Guinea

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Die Shoshonit Porphyry Cu-Au Assoziation im Goonumbla Distrikt, N.S.W., Australien

Zusammenfassung Die Porphyry Cu-Au Vererzung im Goonumbla Distrikt in New South Wales, Australien, sitzt in oberordovizischen (ca. 439.2 ± 1.2 Ma) Shoshoniten auf. Das petrographische Spektrum dieser Gesteine reicht von andesitischen bis dazitischen Laven und Tuffen, die lokal von Monzonit-Stöcken intrudiert werden; die Gesteine besitzen hohe, aber variable Al₂O₃ Gehalte (13.4–19.9 Gew%), sehr hohe K₂O Gehalte (bis zu 6.8 Gew%) und hohe K₂O/Na₂O Verhältnisse (0.58–1.48), die typisch sind für Shoshonite. Außerdem weisen sie hohe Konzentrationen an LILE Elementen (Ba bis 1200 ppm, Sr bis 1350 ppm) auf und geringe Konzentrationen an HFSE (TiO₂ < 0.67 Gew%, Zr < 125 ppm, Nb < 10 ppm, Hf < 3.4 ppm) sowie an LREE (La < 22.4 ppm, Ce < 31 ppm), die als typisch gelten für potassische Vulkanite von ozeanischen Plattengrenzen.Die Mineralchemie von repräsentativen Glimmer- und Apatit-Phänokristallen ist charakterisiert durch hohe SrO und BaO Gehalte (Glimmer: 0.15 Gew%, bzw. bis 0.28 Gew%; Apatite: bis 0.28 Gew%, bzw. 0.19 Gew%). Sie enthalten ferner sehr hohe Halogen-Konzentrationen. Die Glimmer enthalten beispielsweise bis zu 3.9 Gew% F und 0.14 Gew% Cl, während Apatite bis zu 3.6 Gew% F und 0.68 Gew% Ci aufweisen. Dies erscheint nicht ungewöhnlich, weil Glimmer und Apatite von vererzten Mag matiten zumeist deutlich höhere Halogengehalte besitzen, als solche von unvererzten Magmatiten. Die hohen Halogen-Gehalte in Phänokristallen aus den Shoshoniten legen nahe, die Vulkanite als den Ursprung der Vererzung zu interpretieren.Die Cu-Au Vererzung besteht überwiegend aus den Sulfiden Bornit, Kupferkies, Kupferglanz und vereinzelt auftretendem Pyrit und Tetrahedrit. Gediegen Gold wird in der Regel nur als kleine Partikel innerhalb von Silikaten der shoshonitischen Wirtsgesteine und seltener als feine Einschlüsse in Sulfiden gefunden.Die Vererzung wird von hydrothermaler Alteration der Wirtsgesteine begleitet und zwei Alterationsarten lassen sich unterscheiden: eine potassische sowie eine regional zu beobachtende propylitische Alteration.Die Porphyry Cu-Au Lagerstätte im Goonumbla Gebiet ist ein Beispiel für die weltweit beobachtete Assoziation von Bunt- und Edelmetallvererzungen und potassisch/shoshonitischem Magmatismus. Der Goonumbla Distrikt stellt die älteste bisher bekannte Porphyry Cu-Au Lagerstätte aus einerspätgenetischen ozeanischen Plattengrenze dar. Einmodernes Beispiel für eine Cu-Au Lagerstätte vergleichbaren Typs ist Ladolam auf Lihir Island, Papua New Guinea.

     

Synthetic zeolites formed from expanded perlite: Type,formation conditions and properties

Summary The starting material used was expanded perlite with a grain size < 40 m (74.5 wt.% SiO₂; 12.5 wt.% Al₂O₃). This material is a waste product obtained during the production of expanded perlite. The experiments were carried out with KOH solutions, mixtures of KOH and NaOH solutions (1:1) as well as NaOH solutions in the concentration range 0.5 N to 6.0 N at temperatures of between 100° and 140°C and with reaction periods of 2 hours to 13 days in closed system. In the experiments with KOH containing solutions zeolite ZK-19 (phillipsite), W (merlinoite), G (chabazite) and F (edingtonite) formed. Without addition of aluminium high percentages of zeolite ZK-19 (80–100 wt.%) and zeolite W (90–100 wt.%) were obtained. The addition of aluminium rendered possibly the formation of 90 to 100 wt.% of zeolite G and 85 to 100 wt.% of zeolite F, respectively. In the experiments with NaOH solutions analcime, zeolite Na-Pc (gismondine), zeolite HS (sodalite hydrate) and zeolite A formed. High percentages of zeolite Na-Pc (90–100 wt.%), zeolite HS (up to 100 wt.%) and analcime (up to 100 wt.%) were synthesized without addition of aluminium. The formation of high percentages of zeolite A (95–100 wt.%), however, needs the addition of aluminium, NaCI and seed crystals. The temperature stability of the zeolites decreases in the following sequence: K-F > K-W K-ZK-19 (Na), K-W Na, K-F G_si-rich (Na), K-ZK-19 >> Na-Pc G_si-poor. Zeolite A has a very good temperature stability up to temperatures of } 550 °C similar to that of zeolite K-W. At higher temperatures, however, its stability is very poor. The NH₄ ⁺-exchange capacities (meq/g) of the different zeolites amount to the following values: ZK-19:2.8 - 3.2; W:3.0 - 3.2; G:2.3 - 3.6; A:3.1 - 3.2; Na-Pc:3.5 - 3.6; F : 3.9 - 4.8.

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Zeolithsynthese aus Blähperlit—Art, Bildungsbedingungen und Eigenschaften

Zusammenfassung Ausgangsmaterial der experimentellen Untersuchungen war Blähperlit mit einer Korngröße < 40 ,m (74,5 Gew.-% SiO₂; 12,5 Gew.-% Al₂O₃). Dieses Material ist ein Abfallprodukt, das bei der Produktion von Blähperlit anfällt. Die Experimente wurden mit KOH-Lösungen, Lösungsgemischen aus KOH und NaOH (1:1) sowie mit NaOH-Losungen im Konzentrationsbereich 0,5 n-6,0 n bei Temperaturen von 100° – 140°C und über Reaktionszeiten von 2 Stunden bis zu 13 Tagen im geschlossenen System durchgeführt. In den Experimenten mit KOH-hältigen Lösungen bildeten sich die Zeolithe ZK-19 (Phillipsit), W (Merlinoit), G (Chabasit) und F (Edingtonit). Hohe Prozentgehalte an Zeolith ZK-19 (80 – 100 Gew.-%) und Zeolith W (90–100 Gew.-%) entstehen nur ohne Zugabe von Aluminium. Die Bildung von 90–100 Gew.-% Zeolith G bzw. 85–100 Gew. % Zeolith F ist dagegen durch die Zugabe von Aluminium möglich. In den Experimenten mit NaOH-Lösungen bildeten sich die Zeolithe Analcim, Na-Pc (Gismondin), HS (Sodalithhydrat) und Zeolith A. Hohe Prozentanteile an Zeolith Na-Pc (90–100 Gew.-%), HS (bis zu 100 Gew. %) und Analcim (bis zu 100 Gew.-%) wurden ohne Aluminium-Zugabe synthetisiert. Die Bildung von hohen Gehalten an Zeolith A (95–100 Gew. %) ist jedoch nur unter Zugabe von Aluminium, NaCl und Kristallkeimen möglich.Die Temperaturbeständigkeit der Zeolithe nimmt in der folgenden Reihenfolge ab: K-F > K-W - K-ZK-19 (Na), K-W Na, K-F G_si-reich (Na), K-ZK-19 >> Na-Pc G_si-am. Zeolith A weist bis zu Temperaturen von etwa 550°C eine gute Temperaturbeständigkeit auf, die in etwa der von Zeolith K-W entspricht. Bei höheren Temperaturen ist die Beständigkeit jedoch sehr gering.Die NH⁴⁺-Austauschkapazitäten (mÄqu/g) der verschiedenen Zeolithe erreichen folgende Werte: ZK-19:2,8 - 3,2; W:3,0 - 3,2; G:2,3 - 3,6; A:3,1 - 3,2; Na-Pc:3,5 -3,6; F:3,9 - 4,8.

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With 2 Figures