Application of the QUILF thermobarometer to the peralkaline trachytes and pantellerites of the Eburru volcanic complex, East African Rift, Kenya

The Quaternary Eburru volcanic complex in the south-central Kenya Rift consists of pantelleritic trachytes and pantellerites. The phenocryst assemblage in the trachytes is sanidine + fayalite + ferrohedenbergite + aenigmatite ± quartz ± ilmenite ± magnetite ± pyrrhotite ± pyrite. In the pantellerites, the assemblage is sanidine + quartz + ferrohedenbergite + fayalite + aenigmatite + ferrorichterite + pyrrhotite ± apatite, although fayalite, ferrohedenbergite and ilmenite are absent from more evolved rocks (e.g. with SiO₂ > 71%). QUILF temperature calculations for the trachytes range from 709 to 793 °C and for the pantellerites 668–708 °C, the latter temperatures being among the lowest recorded for peralkaline silicic magmas. The QUILF thermobarometer demonstrates that the Eburru magmas crystallized at relatively low oxidation states (ΔFMQ + 0.5 to − 1.6) for both trachytes and pantellerites. The trachytes and pantellerites evolved along separate liquid lines of descent, the trachytes possibly deriving from a more mafic parent by fractional crystallization and the pantellerites from extreme fractionation of comenditic magmas.     

On the Importance of Geolithological Features for the Estimate of the Site Response: The Case of Catania Metropolitan Area (Italy)

The evaluation of seismic site response in the urban area of Catania was tackled by selecting test areas having peculiar lithological and structural features, potentially favourable to large local amplifications of ground motion. The two selected areas are located in the historical downtown and in the northern part of Catania where the presence of a fault is evident. Site response was evaluated using spectral ratio technique taking the horizontal- to-vertical component ratio of ambient noise. Inferences from microtremor measurements are compared with results from synthetic accelerograms and response spectra computed at all drillings available for this area. Such method is particularly suitable in urban areas where the nature of the outcropping geological units is masked by city growth and anthropic intervention on the surface geology. The microtremor H/V spectral ratios evaluated at soft sites located within the downtown profile tend to be smaller than that usually reported in the literature for such soils. A tendency for amplifications to peaks near 2 Hz is observed only in some sites located on recent alluvial deposits. Evidences for amplifications of site effects (frequency range 4–8 Hz) were observed in the sampling sites located on the fault, with a rapid decrease of spectral amplitude just a few tenths of metres away from the discontinuity. Numerical simulations evidenced the importance of geolithological features at depth levels even greater than 20–30 m. Besides this, the results strongly confirm the importance of the subsurface geological conditions, in the estimate of seismic hazard at urban scale.     

A framework for an optimised groundwater monitoring network and aggregated indicators

The implementation of the Water Framework Directive (EU 2000) requires a groundwater quality monitoring. It is used for characterisation of the ‘good’ chemical status of each groundwater body and for the restoration or protection purposes of those bodies already at ‘good’ status. Interpretative aspects are lying in the design of monitoring network and in the way of building global indicators. Attention is given here to the global chemical status of the groundwater bodies and to the role of diffuse pollution, much of which is brought via groundwater to surface water. Monitoring ‘local’ pollution associated with individual sites is not addressed. Groundwater bodies with different contrasted hydrogeology conditions, land use and topography have been considered to establish an approach for choosing an optimised monitoring network. Then, a quality assessment system has been developed and applied for qualifying the general status of each groundwater body. The use of non-dimensional indexes allows us to process with all kinds of chemical parameters in a normalised way and, by means of adequate aggregation rules, to qualify the general quality status of a groundwater body. The obtained diagnostic, even if not fully validated, is closely linked to the pragmatic objectives contained in the EU Water Directive.     

Geochemistry of silicic magmas in the Macolod Corridor, SW Luzon, Philippines: evidence of distinct, mantle-derived, crustal sources for silicic magmas

Silicic volcanic deposits (>65 wt% SiO₂), which occur as domes, lavas and pyroclastic deposits, are relatively abundant in the Macolod Corridor, SW Luzon, Philippines. At Makiling stratovolcano, silicic domes occur along the margins of the volcano and are chemically similar to the silicic lavas that comprise part of the volcano. Pyroclastic flows are associated with the Laguna de Bay Caldera and these are chemically distinct from the domes and lavas at Makiling stratovolcano. As a whole, samples from the Laguna de Bay Caldera contain lower concentrations of MgO and higher concentrations of Fe₂O_3(t) than the samples from domes and lavas. The Laguna de Bay samples are more enriched in incompatible trace elements. The silicic rocks from the domes, Makiling Volcano and Laguna de Bay Caldera all contain high alkalis and high K₂O/Na₂O ratios. Melting experiments of primitive basalts and andesites demonstrate that it is difficult to produce high K₂O/Na₂O silicic magmas by fractional crystallization or partial melting of a low K₂O/Na₂O source. However, recent melting experiments (Sisson et al., Contrib Mineral Petrol 148:635–661, 2005) demonstrate that extreme fractional crystallization or partial melting of K-rich basalts can produce these silicic magmas. Our model for the generation of the silicic magmas in the Macolod Corridor requires partial melting of mantle-derived, evolved, moderate to K-rich, crystallized calc-alkaline magmas that ponded and crystallized in the mid-crust. Major and trace element variations, along with oxygen isotopes and ages of the deposits, are consistent with this model. Electronic Supplementary Material Supplementary material is available for this article at     

The changing role of hydrogeology in semi-arid southern and eastern Africa

Much of southern and eastern Africa is semi-arid and heavily groundwater dependent. Borehole drilling commenced over a hundred years ago with magnetic and electrical resistivity surveys for borehole siting being introduced from 1936. Formalised training of hydrogeologists led in the 1970s to an almost standard approach to hydrogeological investigation and a period of stability followed, during which some major investigations were carried out. A period of decentralisation and fragmentation has since taken place in many parts of southern and eastern Africa, and groundwater monitoring and management are inadequate in many countries. All but six of the 14 SADC (Southern African Development Community) member states reportedly have an adequate monitoring network in place. However, groundwater demand is increasing and hydrogeologists need to promote the use of appropriate methodologies as an essential part of tackling the severe issues now facing the water sector in the region.     

P-T paths and problems of high-temperature polymetamorphism

Many Precambrian granulite-facies metamorphic complexes contain so-called straight gneisses, which are massive rocks with a clearly pronounced blastomylonitic texture, lineation, and gneissosity. These rocks occur exclusively in high-temperature ductile shear zones, which can develop either during the primary exhumation of rock complexes or during the overprinting by high-temperature dynamometamorphism. The main criterion for distinguishing between these two types of straight gneisses is the configuration of their P-T trajectories, which are recorded in the mineral assemblages in these rocks and their host gneisses. Ductile shear zones developed in Archean granulite gneisses simultaneously with their exhumation, and, hence, their P-T trajectories are segments of decompression and/or isobaric cooling paths. Straight gneisses in Proterozoic polymetamorphic complexes commonly compose high-temperature ductile shear zones overprinted on Archean granulite complexes, and the P-T paths of these rocks are Z-shaped. This means that, at a constant pressure in the middle part of the continental crust, the T _min of the older P-T trajectory corresponded to T _max of the younger trajectory, and often T _max–T _min > 100°C. Such ductile shear zones commonly have a strike-slip morphology and can be easily seen in aerial photographs and discerned during structural geological surveying. These zones can overprint older gneisses without any notable thermal effect on the latter. Relations of this type were identified in the granulite complexes of Limpopo in South Africa, Sharyzhalgai in the southwestern Baikal area, and Lapland in the Kola Peninsula. The results of our research propose a solution for the well-known problem of the significant discrepancies between the isotopic ages in high-temperature-high-pressure complexes and the partial or complete distortion of radiogenic isotopic systems under the effect of a newly inflowing metamorphic fluid. The application of geochronologic techniques to these situations is senseless, and only P-T trajectories provide insight into the actual age relations between the discrete tectono-metamorphic stages. It is thus expedient to conduct not only structural studies of metamorphic complexes but also their detailed petrological examination and the calculation of their P-T paths before geochronologic dating.     

Distribution of cadmium, chromium, copper, lead and zinc in marine sediments in Hong Kong waters

Partitioning of heavy metals (Cd, Cr, Cu, Pb, Zn) in marine sediments collected from various sites in Hong Kong waters were determined using sequential extraction method. Sediments from Kellette Bank, located in Victoria Harbour, had higher metal concentrations especially Cu and Zn than most other sites. Slightly over 20% of total Cu and Cr existed as readily available forms in Peng Chau and Kellette Bank. At most sampling sites, over 15% of the Cu existed as the exchangeable form indicating that Cu could be readily released into the aqueous phase from sediments. A significantly higher percentage of Pb and Zn was associated with the three non-residual fractions. Hence, there is a greater environmental concern for remobilization of Pb and Zn compared with Cr. The high amount of residual Cd (>50%) and the relatively lower Cd content indicate that little environmental concern is warranted for the remobilization of Cd. Distribution of metals in sediments collected from different depth at Kellette Bank shows that metal concentrations decreased with profile depth. The levels of Pb and Zn associated with the two readily available fractions increased sharply in the surface sediment. These metals represented the pollutants, which were introduced into the area in the mid-eighties through early nineties as a result of rapid economic and industrial development in the territory. As significant portions of these metals were bound to the readily available phases in the surface sediments, metal remobilization could be a concern. An erratum to this article can be found at     

Equation of state of MgGeO3 perovskite to 65 GPa: comparison with the post-perovskite phase

The equation of state of MgGeO₃ perovskite was determined between 25 and 66 GPa using synchrotron X-ray diffraction with the laser-heated diamond anvil cell. The data were fit to a third-order Birch–Murnaghan equation of state and yielded a zero-pressure volume (V ₀) of 182.2 ± 0.3 Å³ and bulk modulus (K ₀) of 229 ± 3 GPa, with the pressure derivative (K′₀ = (?K ₀/?P) _T ) fixed at 3.7. Differential stresses were evaluated using lattice strain theory and found to be typically less than about 1.5 GPa. Theoretical calculations were also carried out using density functional theory from 0 to 205 GPa. The equation of state parameters from theory (V ₀ = 180.2 Å³, K ₀ = 221.3 GPa, and K′₀ = 3.90) are in agreement with experiment, although theoretically calculated volumes are systematically lower than experiment. The properties of the perovskite phase were compared to MgGeO₃ post-perovskite phase near the observed phase transition pressure (～65 GPa). Across the transition, the density increased by 2.0(0.7)%. This is in excellent agreement with the theoretically determined density change of 1.9%; however both values are larger than those for the (Mg,Fe)SiO₃ phase transition. The bulk sound velocity change across the transition is small and is likely to be negative [?0.5(1.6)% from experiment and ?1.2% from theory]. These results are similar to previous findings for the (Mg,Fe)SiO₃ system. A linearized Birch–Murnaghan equation of state fit to each axis yielded zero-pressure compressibilities of 0.0022, 0.0009, and 0.0016 GPa^?1 for the a, b, and c axis, respectively. Magnesium germanate appears to be a good analog system for studying the properties of the perovskite and post-perovskite phases in silicates.     

The SHAND quaternary system for evaluating the supersilicic or subsilicic crystal-chemistry of eclogite minerals, and potential new UHPM pyroxene and garnet end-members

Summary The stoichiometry of pyroxenes {^viiiX^{2+ vi}Y^{2+ iv}Z⁴⁺ ₂ O₆} and garnets {^xiiX²⁺ ₃ ^viY³⁺ ₂ ^ivZ⁴⁺ ₃ O₁₂} is re-evaluated by a theoretical crystal-chemical approach that takes into account natural phenomena that do not fit with conventional anhydrous stoichiometric mineralogy: the existence in eclogites of microinclusions of other minerals that may have been exsolved from previous supersilicic or subsilicic UHPM pyroxene or garnet. Different definitions of supersilicic and subsilicic are discussed and the one based on the ability to exsolve SiO₂ and leave behind a stoichiometric pyroxene or garnet is recommended for general adoption. The SHAND system (S = Si et al.; H = H; A = Al et al.; N = Na et al.; D = divalents) for projecting multivariate chemical space involving 23 cations and 104 selected natural or potential mineral species on to two essential diagrams (SAND and SHND) is described in full for the first time. Numerous possible chemical exchanges are considered and justified with respect to known mineral phenomena such as cation vacancies, octahedral silicon or protonation. Several new potential end-members are presented, in particular “supersilipyx”, “supersiligar” and “subsiligar”. It is suggested that small quantities of these end-members can be incorporated into UHPM solid-solutions and lead to various exsolution phenomena during eclogite exhumation.