Sr-isotope stratigraphy of the Upper Jurassic of central Portugal (Lusitanian Basin) based on oyster shells

Strontium isotope stratigraphy was performed on oyster shells from the Late Jurassic of the Lusitanian Basin (central Portugal). This represents the first approach to obtain numerical ages for these strata. The new chronostratigraphic data provide a more precise age determination of several units. After a basin-wide hiatus sedimentation in the Late Jurassic is proven in the Cabo Mondego and Cabaços formations to resume as early as the Middle Oxfordian. The Alcobaça formation can be placed in the latest Late Oxfordian to Late Kimmeridgian, while data from the upper part of the Abadia Formation indicate an Early to Late Kimmeridgian age. The Farta Pao formation ranges from the latest Kimmeridgian to the latest Tithonian. The largely synchronous Sobral, Arranhó I, and Arranhó II members are overlain by the late Early to Late Tithonian Freixial Member. The brief, local carbonate incursion of the Arranhó I member marks the Kimmeridgian–Tithonian boundary. Oysters are shown once more to be suitable for strontium isotope studies. Their calcitic shells are often unaffected by diagenesis. In particular for marginal marine Jurassic and Cretaceous strata, where belemnites are usually absent, oysters may serve as a valuable tool for isotope stratigraphy.     

Hydrothermal models of the Perth metropolitan area, Western Australia: implications for geothermal energy

Hydrothermal simulations are used to provide insight into the subsurface thermal regime of the Perth metropolitan area (PMA) in Western Australia. High average permeabilities and estimated fluid flow rates in shallow aquifers of the PMA suggest that advection and convection may occur in these aquifers. These processes are simulated, using a new geological model of the PMA to constrain the geometry of aquifers, aquitards and faults. The results show that advection has a strong influence on subsurface temperature, especially in the north of the PMA, where aquifer recharge creates an area of anomalously low temperature. Convection may be important, depending on the permeability of the Yarragadee Aquifer. If convection occurs, it creates thermal highs and lows with a spacing of approximately 5 km. Some of these thermal anomalies migrate over geological time due to coupling between advection and convection, but they are stationary on human timescales. Fault permeability influences the pattern of convection. Advection and convection cause variations in the geothermal gradient which cannot be predicted by conductive models; therefore, these processes should be considered in any model that is used for assessment of geothermal resources in the PMA.     

Total nitrogen content of deep sea basalts

Various models have been suggested concerning the origin and evolution of the earth's atmosphere. An estimate of the nitrogen content of the mantle could further constrain atmospheric models. Total nitrogen content was determined by thermal neutron activation analysis via ¹⁴N(n,p)¹⁴C. The ¹⁴C was converted to carbon dioxide and counted in miniature low level proportional counters. The total nitrogen content of U.S.G.S. standards BCR-1 and G-2 as determined by different laboratories is variable, probably due to atmospheric adsorption by the finely ground samples. Total nitrogen content was determined in deep sea basalt glasses from three regions: East Pacific Rise ($\text{15 ± 4, 18 ± 4}$, and $\text{7 ±}\text{ppm}\text{2 N}$), Mid-Atlantic Rift (FAMOUS Region:$\text{22 ± 5, 18 ± 3}$, and $\text{10 ± 2}\text{ppm}\text{N}$) and the Juan de Fuca Ridge ($\text{17 ± 4}\text{ppm}\text{N}$). Matrix material from the same samples as the glasses was available from the East Pacific Rise ($\text{37 ± 6, 26 ± 4}$, and $\text{34 ± 6}\text{ppm}\text{N}$) and the Mid-Atlantic Rift ($\text{39 ± 4}\text{ppm}\text{N}$) which are about 50 to 100% greater than the associated glasses. The increased matrix abundance may be due to incorporation of chemically bound nitrogen from sea water rather than dissolved molecular nitrogen. The nitrogen content of the FAMOUS samples are inconsistent with the model of Langmuir et al. (1977) for petrogenesis based on trace element data. Factors which can affect the observed nitrogen content in the basalts and the interpretation in terms of the mantle nitrogen abundance are discussed (e.g. partial melting and degassing of the basalts). A lower limit of about 2 ppm N in the mantle can be estimated.     

Thermal evolution of the central Halls Creek Orogen,northern Australia

The Halls Creek Orogen in northern Australia records the Palaeoproterozoic collision of the Kimberley Craton with the North Australian Craton. Integrated structural, metamorphic and geochronological studies of the Tickalara Metamorphics show that this involved a protracted episode of high‐temperature, low‐pressure metamorphism associated with intense and prolonged mafic and felsic intrusive activity in the interval ca 1850–1820 Ma. Tectonothermal development of the region commenced with an inferred mantle perturbation event, probably at ca 1880 Ma. This resulted in the generation of mafic magmas in the upper mantle or lower crust, while upper crustal extension preceded the rapid deposition of the Tickalara sedimentary protoliths. An older age limit for these rocks is provided by a psammopelitic gneiss from the Tickalara Metamorphics, which yield a ²⁰⁷Pb/²⁰⁶Pb SHRIMP age of 1867 ± 4 Ma for the youngest detrital zircon suite. Voluminous layered mafic intrusives were emplaced in the middle crust at ca 1860–1855 Ma, prior to the attainment of lower granulite facies peak metamorphic conditions in the middle crust. Locally preserved layer‐parallel D₁ foliations that were developed during prograde metamorphism were pervasively overprinted by the dominant regional S₂ gneissosity coincident with peak metamorphism. Overgrowths on zircons record a metamorphic ²⁰⁷Pb/²⁰⁶Pb age of 1845 ± 4 Ma. The S₂ fabric is folded around tight folds and cut by ductile shear zones associated with D₃ (ca 1830 Ma), and all pre‐existing structures are folded around large‐scale, open F₄ folds (ca 1820 Ma). Construction of a temperature‐time path for the mid‐crustal section exposed in the central Halls Creek Orogen, based on detailed SHRIMP zircon data, key field relationships and petrological evidence, suggests the existence of one protracted thermal event (>400–500°C for 25–30 million years) encompassing two deformation phases. Protoliths to the Tickalara Metamorphics were relatively cold (～350°C) when intruded by the Fletcher Creek Granite at ca 1850 Ma, but were subsequently heated rapidly to 700–800°C during peak metamorphism at ca 1845 Ma. Repeated injection of mafic magmas caused multiple remelting of the metasedimentary wall rocks, with mappable increases in leucosome volume that show a strong spatial relationship to these intrusives. This mafic igneous activity prolonged the elevated geotherm and ensured that the rocks remained very hot (≥650°C) for at least 10 million years. The Mabel Downs Tonalite was emplaced during amphibolite facies metamorphism, with intrusion commencing at ca 1835 Ma. Its compositional heterogeneity, and the presence of mutual cross‐cutting relations between ductile shear zones and multiple injections of mingled magma suggest that it was emplaced syn‐D₃. Broad‐scale folding attributable to F₄ was accompanied by widespread intrusion of granitoids, and F₄ fold limbs are truncated by large, mostly brittle retrograde S₄ shear zones.     

Fluid inclusion studies of the Abawso gold prospect,near the Ashanti Belt,Ghana

The major Ghanaian lode gold deposits are preferentially aligned along the western and eastern contacts of the Kumasi Basin with the Ashanti and Sefwi Belts, respectively. The investigated area of the Abawso small-scale concession, covering the workings of the old Ettadom mine, is situated 3 km west of the lithological contact of the Birimian metavolcanic rocks of the Akropong Belt in the east with the Birimian metasedimentary rocks of the Kumasi Basin in the west. The rocks of the Abawso concession represent a steeply NW-dipping limb of a SE-verging anticline with an axis plunging to the SW. Quartz veining occurs predominantly in the form of en échelon dilatational veins along NNE–SSW-striking shear zones of a few metres width and shows evidence of brittle and ductile deformation. Also stockwork-style quartz veining occurs in the vicinity of the main shaft of the old Ettadom mine. Hydrothermal alteration includes sericitisation, sulphidation and locally carbonatisation. The auriferous quartz veins mainly follow the trend of brittle to ductile deformed quartz veins; however, some occur in stockwork. Fluid inclusion studies reveal a large number of H₂O inclusions along intragranular trails in auriferous quartz vein samples, as well as an overall dominance of H₂O and H₂O-CO₂ inclusions over CO₂ inclusions. Textural observations and physico-chemical fluid inclusion properties indicate post-entrapment modifications for all quartz vein samples due to grain boundary migration recrystallisation. This process is interpreted to be responsible for the generation of the CO₂ inclusions from a H₂O-CO₂ parent fluid. In comparison with mineralisation at the Ashanti and Prestea deposits, which are characterised by CO₂±N₂ inclusions, the observed inclusion assemblage may be due to a shallower crustal level of mineralisation, or different degrees and styles of recrystallisation, or a less pronounced development of laminated quartz veins due to comparably restricted pressure fluctuations. Furthermore, the microthermometric observations allow the reconstruction of a possible retrograde P-T path, depicting near-isothermal decompression in the P-T range of the brittle/ductile transition.Editorial handling: E. Frimmel     

Experimental studies on the phase systems Fe-Ni-Pd-S and Fe-Pt-Pd-As-S applied to PGE deposits

Summary In the present paper current results of experimental investigation of the phase system Pd-Fe-Ni-S at 900°C, 725°C, 550°C and 400°C as well as of the phase system Pt-Fe-As-S at 850°C and 470°C are summarized. A preliminary note on the system Pt-Pd-As-S is added. Individual phase assemblages are presented, data on solubility of PGE in base metal sulphides/arsenides or alloys are given and solid solution ranges of important minerals are described as a function of temperature and phase assemblage. The extent and role of sulphide/arsenide melts in these systems are presented together with hints for, and examples of the application of the current experimental results for the explanation of ore-geological processes.

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Bisherige Ergebnisse experimenteller Untersuchungen in den Systemen Fe-Ni-Pd-S und Fe-Pt-Pd-As-S und ihre Bedeutung für Lagerstätten der Platin-Gruppen-Elemente

Zusammenfassung In der vorliegenden Arbeit werden bisherige Ergebnisse experimenteller Untersuchungen in den Phasensystemen Pd-Fe-Ni-S bei 900°C, 725°C, 550°C sowie 400°C, bzw. Pt-Fe-As-S bei 850°C und 470°C zusammengefasst. Vorläufige Anmerkungen zum System Pt-Pd-As-S werden gegeben. Die Phasenbeziehungen und die Löslichkeitsdaten von PGE's in Buntmetall-Sulfiden/Arseniden sowie deren Verbindungen werden präsentiert. Die Mischungsbereiche der wichtigsten Minerale werden als Funktion von Temperatur und Phasenvergesellschaftung diskutiert. Die Rolle von Sulfid/Arsenid Schmelzen in diesen Systemen und Beispiele für die Anwendung dieser experimentellen Ergebnisse zur Erklärung lagerstättenkundlicher Prozesse werden beschrieben.

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With 6 Figures     

Dike rock generation and magma interactions in the Bir Safsaf igneous complex,south-west Egypt: Implications for the Pan-African evolution in north-east Africa

The geological setting, ages, petrography and geochemistry of late Pan-African ( 580 Ma) calc-alkaline and tholeiitic dike rocks in the Bir Safsaf igneous complex of south-west Egypt are discussed. These basaltic to rhyolitic dikes intruded contemporaneously and shortly after the intrusion of granitoids. The major and trace element data, Sr and Nd isotope relations, in combination with textural observations, confirm complex interactions between most of the intermediate calcalkaline dike melts and plutonic melts, with different degrees of mixing, assimilation, replenishment and tapping of magma chambers. Trachytic and rhyolitic dikes are strongly differentiated melts from the granitic pluton. The tholeiitic dikes evolved dominantly by fractional crystallization processes. It is inferred that open system and closed system processes operated in calc-alkaline magma chambers, and that the calc-alkaline melts came from a garnet-and amphibole-bearing mantle, modified by a subduction component. Tholeiitic rocks were formed later by fractional crystallization and assimilation processes. Magma ascent of both dike types took place in an extensional environment and the presumed subduction zone has to be seen in connection with the Atmur-Delgo suture zone.     

Redistribution of HFSE elements during rutile replacement by titanite

Titanite growth at the expense of rutile during retrograde hydration of eclogite into amphibolite is a common phenomenon. We investigated an amphibolite sample from the Tromsø eclogite facies terrain in Northern Norway to gain insight into the trace element distribution between rutile and titanite during incomplete resorption of the rutile by titanite. Patchy compositional zoning of Al, Ti, and F in titanite relates to the presence of a fluid with variable Ti/Al and/or F during its growth. Laser ablation ICP–MS and electron microprobe data for high field strength elements (HFSE: Nb, Zr, Ta, and Hf) of rutile resorbed by titanite indicate a pronounced enrichment of these elements in the rim of a large single rutile crystal (~8 mm) and a systematic decrease towards uniform HFSE contents in the large core. HFSE contents of smaller rutile grains (~0.5 mm) and rutile inclusions (<100 μm) in the titanite overgrowth are similar or higher than in the rims of large rutile crystals. Element profiles from the rim inward demonstrate that HFSE enrichment in rutile is controlled by diffusion. HFSE ratios in diffusion-altered rutile show systematic variations compared with the uniform core composition of the large rutile. Modelling of Zr and Nb diffusion in rutile indicates that diffusion coefficients in rutile in fluid-dominated natural systems must be considerably higher than those determined experimentally at 1 bar in dry systems. Variations of HFSE contents in the newly formed titanite show no systematic spatial distribution. HFSE ratios in titanite and the rims of rutile are different, indicating different solid/fluid distribution coefficients in these minerals. Element fractionation by diffusion into the relict rutile and during fluid-mediated growth of new titanite could substantially change the HFSE budget of these minerals and could affect their use for geochemical tracing and other applications, such as Zr-based geothermobarometry.