Kimberlite metasomatism at Murowa and Sese pipes, Zimbabwe

Metasomatism accompanying kimberlite emplacement is a worldwide phenomenon, although infrequently described or recognised. At the Cambrian-aged Murowa and Sese kimberlite clusters located within the Archean Zimbabwe Craton just north of the boundary with the Limpopo Mobile Zone in southern central Zimbabwe, the metasomatism is intense and well exposed and the processes can be readily studied. Dykes, sills and the root zones of pipes are exposed at the current erosion level. Kimberlite lithologies present are hypabyssal macrocrystic kimberlite (“HMK”), HMK breccia, and tuffisitic kimberlite breccia (“TKB”) including minor lithic tuffisitic kimberlite breccia (“LTKB”). Country rocks are 2.6 Ga Chibi and Zimbabwe granite batholiths emplaced into 2.6–2.9 Ga or earlier Archean tonalitic gneiss and greenstones. During initial metasomatism, the granites become spotted with green chlorite, needles of alkaline amphiboles (winchite, riebeckite, arfvedsonite) and pyroxenes (aegirine–augite) with minor carbonate and felts of talc. Oligoclase feldspar becomes converted to albite, extensively altered, dusted and reddened with hematite, whereas K-feldspar remains unaffected. The granites become converted to syenite through removal of quartz. More intense metasomatism at Murowa and Sese results in veins of green metasomatite which cut and disrupt the granite. Progressive disruption entrains granite blocks, breaking down the granite still further, spalling off needle-like granite slivers, and so giving rise to LTKB. This process of disruption and entrainment appears to be the manner of initial development of the pipe structure. The chemistry of the metasomatite is intermediate between granite and kimberlite. Compared to granite country rock it has markedly higher Mg, Cr, Ni, CO₂ and H₂O+, higher Ca, Mn, Nb, Sr, P, Fe³⁺/Fe²⁺ ratio, U, Co, and Cu, approximately equal TiO₂, K₂O, Na₂O, La, Ta, Rb, Zr, Zn and resultant lower SiO₂, Al₂O₃, Ga and Y. The metasomatite Na₂O/K₂O ratio is slightly higher than that of the granite. The metasomatic process is broadly analogous to fenitisation of granitic wall rock accompanying carbonatite complex emplacement. The metasomatism at Murowa and Sese was caused by fluids from the rising but confined proto-kimberlite melt penetrating into cracks and matrix of granite country rock and reacting with it. These fluids were CO₂-rich, hydrous, oxidising, enhanced in ultramafic elements and carried low levels of Na.     

Propagation of the Southwest Indian Ridge at the Rodrigues Triple Junction

The analysis of multibeam bathymetric data of the Southwest Indian Ridge(SWIR) domain between the triple junction traces from 68° E to theRodrigues Triple Junction (RTJ; 70° E) reveals the evolution of thisridge since magnetic anomaly 4 (8 Ma). Image processing has been used toshow that the horizontal component of strain due to a network of normal stepfaults increases dramatically between 69°30 E and the RTJ. Thisarea close to the RTJ is characterized by a deep graben at the foot of thetriple junction trace on the African plate and by a narrow fault-boundedridge that joins an offset of the trace on the Antarctic plate. In thatarea, spreading is primarily amagmatic and dominated by tectonic extensionprocesses. To the west of 69°30 E, some lobate bathymetricfeatures atop of a large topographic high suggest volcanic constructions.Between 68°10 E and 69°25 E the southern flank of theSWIR domain is wider than the northern one and is characterized by a series of 7 en echelon bathymetric highs similar in size,shape and orientation to the one centred at 69°30E near the present-day triple junction. Their en echelon organization along the triple junction trace on the Antarctic plate and the typical lack of conjugated parts on the northern flank show that these bathymetric highs have been shifted to the south by successive northward relocalisations of the SWIR rifting zone. This evolution results in the asymmetric spreading of the SWIR in the survey area. The off-axis bathymetric highs connect to the offsets of the triple junction trace on the Antarctic plate when the Southeast Indian Ridges lightly lengthenstoward the northwest and the triple junction is relocated to the north. We propose that the SWIR lengthens toward the northeast with two propagation modes: 1) a continuous and progressive propagation with distributed deformation in preexisting crust of the Central Indian Ridge, 2) a discontinuous propagation with focusing of the deformation in a rift zone when the triple junction migrates rapidly to the north. The modes of propagation of the SWIR are related to different localisation and distribution of strain which are in turn controlled by changes of the triple junction configurations due to propagation, recession or a symmetric spreading on the Central and Southeast Indian Ridges.     

Chemical ozone loss in the Arctic vortex in the winter 1995–96: HALOE measurements in conjunction with other observations

Severe chemical ozone loss has been detected in the Arctic in the winter and spring of 1995–96 by a variety of methods. Extreme reductions in column ozone due to halogen catalysed chemistry were derived from measurements of the Halogen Occultation Experiment (HALOE) on board the Upper Atmosphere Research Satellite in the Arctic vortex. Here, we discuss further aspects of the HALOE observations in the Arctic over this period. Potential problems, both in the data themselves and in the methodology of the data analysis are considered and the reason for the differences between the Arctic ozone losses deduced from HALOE data version 17 and 18 is analysed. Moreover, it is shown that HALOE measurements in the Arctic in winter and spring 1995–96 compare well with observations by other ground-based and satellite instruments.     

Dynamic evolution of nutrient discharge under stormflow and baseflow conditions in a coastal agricultural watershed in Ishigaki Island,Okinawa, Japan

Excessive terrestrial nutrient loadings adversely impact coral reefs by primarily enhancing growth of macroalgae, potentially leading to a phase‐shift phenomenon. Hydrological processes and other spatial and temporal factors affecting nutrient discharge must be examined to be able to formulate effective measures for reducing nutrient export to adjacent reefs. During storm events and baseflow periods, water samples were obtained from the tropical Todoroki River, which drains an intensively agricultural watershed into Shiraho coral reef. In situ nutrient analyzers were deployed for 6 months to hourly measure dissolved nutrient (NO₃⁻‐N and PO₄³⁻‐P) concentrations. Total phosphorus (TP) and suspended solid concentration (TSS) were increased by higher rainfall intensity (r = 0·94, p < 0·01) and river discharge Q (r = 0·88, p < 0·01). In contrast, NO₃⁻‐N concentration tends to decrease drastically (e.g. from 3 to 1 mg l⁻¹) during flood events. When base flow starts to dominate afterwards, NO₃⁻‐N manifested an increasing trend, but decreases when baseflow discharge becomes low. This counter‐clockwise hysteresis for NO₃⁻‐N highlights the significant influence of groundwater discharge. N delivery can therefore be considered a persistent process compared to sediment and P discharge, which are highly episodic in nature. Based on GIS analysis, nutrient concentration along the Todoroki River was largely affected by the percentage of sugarcane/bare areas and bedrock type. The spatial distribution of N concentration in the river reflects the considerable influence of subsurface geology—higher N levels in limestone‐dominated areas. P concentrations were directly related to the total length of artificial drainage, which enhances sediment transport. The use of high‐resolution monitoring data coupled with GIS‐based spatial analysis therefore enabled the clarification of control factors and the difference in the spatio‐temporal discharge characteristics between N and P. Thus, although erosion‐reduction schemes would reduce P discharge, other approaches (e.g. minimize fertilizer) are needed to reduce N discharge. Copyright © 2010 John Wiley & Sons, Ltd.     

Inverse analysis of deformation mechanism by geodetic surveys−a case study

In 1988 two large earthquakes with magnitude of Ms 7.6 and Ms 7.2 occurred in Lancang-Genma area, Southwest China. This paper discusses the determination of the spatial distribution of fault slip caused by the earthquakes using geodetic surveys. The prior information obtained from geological surveys and seismological investigations was used to determine the geometry of the fault plane and the average fault slip. The smooth constraints on the fault slips have been described by a normal distribution with hyperparameters, which are incorporated in the inversion analysis with a Bayesian model. Akaike’s Bayesian Information Criterion (ABIC) is used to get the optimal values of hyperparameters. Once the hyperparameters are determined, the maximum likelihood method is employed to estimate the patterns of a fault slip. Based on the results of inverse analysis monitoring geodetic surveys can be properly designed and conducted to obtain crust deformations and predict potential earthquake sources.     

Uranium co-precipitation with iron oxide minerals

In oxidizing environments, the toxic and radioactive element uranium (U) is most soluble and mobile in the hexavalent oxidation state. Sorption of U(VI) on Fe-oxides minerals (such as hematite [α-Fe₂O₃] and goethite [α-FeOOH]) and occlusion of U(VI) by Fe-oxide coatings are processes that can retard U transport in environments. In aged U-contaminated geologic materials, the transport and the biological availability of U toward reduction may be limited by coprecipitation with Fe-oxide minerals. These processes also affect the biological availability of U(VI) species toward reduction and precipitation as the less soluble U(IV) species by metal-reducing bacteria.To examine the dynamics of interactions between U(VI) and Fe oxides during crystallization, Fe-oxide phases (containing 0.5 to 5.4 mol% U/(U + Fe)) were synthesized by means of solutions of U(VI) and Fe(III). Wet chemical (digestions and chemical extractions) and spectroscopic techniques were used to characterize the synthesized Fe oxide coprecipitates after rinsing in deionized water. Leaching the high mol% U solids with concentrated carbonate solution (for sorbed and solid-phase U(VI) species) typically removed most of the U, leaving, on average, about 0.6 mol% U. Oxalate leaching of solids with low mol% U contents (about 1 mol% U or less) indicated that almost all of the Fe in these solids was crystalline and that most of the U was associated with these crystalline Fe oxides. X-ray diffraction and Fourier-transform infrared (FT-IR) spectroscopic studies indicate that hematite formation is preferred over that of goethite when the amount of U in the Fe-oxides exceeds 1 mol% U (∼4 wt% U). FT-IR and room temperature continuous wave luminescence spectroscopic studies with unleached U/Fe solids indicate a relationship between the mol% U in the Fe oxide and the intensity or existence of the spectra features that can be assigned to UO₂²⁺ species (such as the IR asymmetric υ₃ stretch for O = U = O for uranyl). These spectral features were undetectable in carbonate- or oxalate-leached solids, suggesting solid phase and sorbed U(VI)O₂²⁺ species are extracted by the leach solutions. Uranium L₃-edge x-ray absorption spectroscopic (XAFS) analyses of the unleached U-Fe oxide solids with less than 1 mol% U reveal that U(VI) exists with four O atoms at radial distances of 2.19 and 2.36 Å and second shell Fe at a radial distance at 3.19 Å.Because of the large ionic radius of UO₂²⁺ (∼1.8 Å) relative to that of Fe³⁺ (0.65 Å), the UO₂²⁺ ion is unlikely to be incorporated in the place of Fe in Fe(III)-oxide structures. Solid-phase U(VI) can exist as the uranyl [U(VI)O₂²⁺] species with two axial U-O double bonds and four or more equatorial U-O bonds or as the uranate species (such as γ-UO₃) without axial U-O bonds. Our findings indicate U⁶⁺ (with ionic radii of 0.72 to 0.8 Å, depending on the coordination environment) is incorporated in the Fe oxides as uranate (without axial O atoms) until a point of saturation is reached. Beyond this excess in U concentration, precipitating U(VI) forms discrete crystalline uranyl phases that resemble the uranyl oxide hydrate schoepite [UO₂(OH)₂·2H₂O]. Molecular modeling studies reveal that U⁶⁺ species could bond with O atoms from distorted Fe octahedra in the hematite structure with an environment that is consistent with the results of the XAFS. The results provide compelling evidence of U incorporation within the hematite structure.