Tectonically dewatered slates in the Ludlovian of the Lake District,England

Multiple siltstone dykes intruded parallel to cleavage in the Ludlovian argillites and graywackes of the Lake District throw new light on the origin of slaty cleavage. Pore pressures equalling lithostatic pressure developed during the Caledonian orogeny and caused tectonic dewatering of the partially lithified sediments. Slaty cleavage was initiated as an essentially planar structure by the intrusion of thin pelitic folia during the escape of the pore water. Cleavage folia and fold axial planes may have a common geometric relationship to the deforming stresses, but are independent of each other in origin. Continued deformation after tectonic dewatering refracted the cleavage by rotation of competent layers. Critical examination of evidence supporting traditional theories of slaty-cleavage formation shows that all observed relationships are compatible with the tectonic-dewatering theory.     

Gold recovery from a refractory pyrrhotite ore by biooxidation

The aim of the present investigation was to study the biooxidation of a refractory gold-bearing pyrrhotite, in order to increase the gold recovery during the subsequent conventional cyanidation.Bacterial cultures utilised in the biological test consisted predominantly of Thiobacillus genus. Tests were conducted at laboratory scale. The gold content of the ore sample, coming from Bolivia, was of 10 g t⁻¹ Au.After 24 h leaching time by direct cyanidation, low gold recovery was obtained (<20% Au), with a high reagent consumption. On the other hand, a high gold recovery was achieved for the biooxidated samples: after 24 h cyanidation gold dissolution reached about 91% Au.Experimental results have shown the technical feasibility of the biooxidative pretreatment prior to conventional leaching and a complete circuit of treatment, on laboratory scale, has been developed considering also the subsequent gold recovery by carbon adsorption/desorption and electrowinning.A gold extraction yield of about 86% was determined in the whole process for gold extraction from pyrrhotite (biooxidation, solid–liquid separation, cyanidation, adsorption, desorption, electrowinning).     

Mineralogy and geochemistry of lateritic soil profiles in Kerala, India

Lateritic soils near Calicut, Kerala, contain halloysite of intermediate hydration, kaolinite, goethite, gibbsite and quartz. The presence of halloysite is responsible for relatively high plasticity and cation-exchange capacity. Fe-hydroxide colloids along with halloysite contribute to significant phosphate uptake by this soil. Composition of local groundwater is consistent with weathering of sodic plagioclase to gibbsite, kaolinite and metastable halloysite.     

Radiating 1.0 Ga Mafic Dyke Swarms of Eastern Brazil and Western Africa: Evidence of Post-Assembly Extension in the Rodinia Supercontinent?

Several mafic dyke swarms of similar composition and age (tholeiite- ca.1.0 Ga) occur on both sides of the Atlantic Ocean in eastern South America and western Africa. When assembled to their pre-drift position in the Mesozoic, the Brazilian coastal dyke province of Bahia, and the African dykes in Cameroun (Ebolowa suite) and Congo (Comba and Sembe-Ouesso provinces) define a giant radiating pattern (1200 km × 800 km) similar to other dyke swarms elsewhere associated with large-scale continental rifting. Magma flow indicators of the Brazilian dykes and branching propagation styles of their African counterparts indicate that the dyke conduits were fed with magmas diverging from a source beneath the long axis of the Meso-Neoproterozoic West-Congolian Basin in Africa. There, MORB-like metabasalts have been described in the La Bikossi Group of the Mayombian Supergroup. Whether the rifting event and intrusion of dyke swarms were triggered or not by a mantle plume beneath part of the Rodinia subcontinental lithosphere remain to be confirmed.     

Characterisation of Memory Effects and Development of an Effective Wash Protocol for the Measurement of Petrogenetically Critical Trace Elements in Geological Samples by ICP-MS

High sensitivity and low detection limits would seem to make inductively coupled plasma-mass spectrometry (ICP-MS) an ideal analytical tool for determining low (sub-μg g^-1) concentrations of the rare earth elements (REE), Y, Zr, Nb, Hf, Ta, Sn, W, Mo, Th, and U in most mafic materials (e.g. Hall and Plant 1992). However, the generally "sticky" nature exhibited by most of the high field strength elements (HFSEs: Zr, Nb, Hf, Ta, Th and U) as well as Sn, W and Mo can result in spurious results due to memory effects transmitted between unknowns and calibration samples. This, in turn, can seriously compromise the sensitivity, accuracy, and precision of ICP-MS analyses for these elements in geological materials. Data resulting from analyses with poor accuracy and precision can lead to erroneous interpretation and misleading petrogenetic modelling. To resolve this problem, we propose an effective wash protocol for these critical trace elements.     

Barium silicates of the Berisal Complex, Switzerland: A study in geochronology and rare-gas release systematics

Barium silicate minerals such as celsian, ganterite, armenite, as well as Ba-bearing and Ba-free white mica from the Berisal Complex, Simplon Nappe, Swiss Alps, were dated by ³⁹Ar-⁴⁰Ar. Ages of Ba-free micas are ca. 17 Ma, while Ba and parentless ⁴⁰Ar are correlated in Ba silicates, suggesting common inheritance from the Paleozoic orthogneissic protolith. The release pattern of reactor-produced ³⁹Ar (or ³⁷Ar) from hydrated and anhydrous minerals is very similar, with apparent activation energies of ca. 180 kJ/mole and a conspicuous kink around 900 °C. White micas release Ar at higher temperature than the literature determination of their dehydroxylation. In addition to Ar, we studied the degassing of monoisotopic ¹³¹Xe produced from Ba during neutron irradiation. Xe is degassed at higher temperature than Ar, and again all analyzed silicates have the same apparent activation energy of ca. 300 kJ/mole. The decoupling of Ar and Xe rules out delamination as the dominant degassing mechanism in mica and implies that recoiled rare gas atoms mostly reside inside the T-O-T layers of the mica structure. The near-identical apparent activation energies in such diverse silicates as tecto-, phyllo- and cyclosilicate requires instead that the in-vacuo gas release kinetics are the same in all three silicates. As the only structural element common to these three silicate families are silica tetrahedra, it is possible that their well-known rotation plays a decisive role for in-vacuo Ar degassing; additional high-temperature in situ structural investigations on feldspars and micas would be needed to help constrain the mechanisms of laboratory Ar release.     

Evidence for the enhanced lability of dissolved organic matter following permafrost slope disturbance in the Canadian High Arctic

Arctic landscapes are believed to be highly sensitive to climate change and accelerated disturbance of permafrost is expected to significantly impact the rate of carbon cycling. While half the global soil organic matter (SOM) is estimated to reside in Arctic soils, projected warmer temperatures and permafrost disturbance will release much of this SOM into waterways in the form of dissolved organic matter (DOM). The spring thaw and subsequent flushing of soils releases the highest contributions of DOM annually but has historically been undersampled due to the difficulties of sampling during this period. In this study, passive samplers were placed throughout paired High Arctic watersheds during the duration of the 2008 spring flush in Nunavut, Canada. The watersheds are very similar with the exception of widespread active layer detachments (ALDs) that occurred within one of the catchments during a period of elevated temperatures in the summer of 2007. DOM samples were analyzed for structural and spectral characteristics via nuclear magnetic resonance (NMR) and fluorescence spectroscopy as well as vulnerability to degradation with simulated solar exposure. Lignin-derived phenols were further assessed utilizing copper(II) oxide (CuO) oxidation and gas chromatography/mass spectrometry (GC/MS). The samples were found to have very low dissolved lignin phenol content (∼0.07% of DOC) and appear to originate from primarily non-woody angiosperm vegetation. The acid/aldehyde ratios for dissolved vanillyl phenols were found to be high (up to 3.6), indicating the presence of highly oxidized lignin. Differences between DOM released from the ALD vs. the undisturbed watershed suggest that these shallow detachment slides have significantly impacted the quality of Arctic DOM. Although material released from the disturbed catchment was found to be highly oxidized, DOM in the lake into which this catchment drained had chemical characteristics indicating high contributions from microbial and/or primary productivity. The resulting pool of dissolved carbon within the lake appears to be more biologically- and photochemically-labile than material from the undisturbed system. These disturbances may have implications for projected climate warming; sustained elevated temperatures would likely perpetuate widespread ALDs and further affect carbon cycling in this environment.     

L'âge radiométrique du Miocène inférieur en Europe Occidentale et Centrale

Systematic research over years on datable horizons of lower Miocene age has led to an election of nine glauconite samples suitable for dating work. The chosen glauconites come from various regions of the tethys. Following careful sedimentological as well as stratigraphical studies the K-Ar ages of these glauconites were measured. The interpretation of the apparent ages found takes into consideration sedimentation, mineralogical quality and present knowledge of the genesis of the green glauconite pellets. The presented data allow to fix the basis of the Miocene at about 21–22 m. y. and the boundary of Aquitanian-Burdigalian at 18 m. y. The K-Ar data on glauconites presented here are in good agreement with newer measurements of other authors on high temperature minerals of the same age span.     

Re–Os isotope and platinum-group element geochemistry of the Pobei Ni–Cu sulfide-bearing mafic–ultramafic complex in the northeastern part of the Tarim Craton

A number of mafic–ultramafic intrusions that host Ni–Cu sulfide mineralization occur in the northeastern Tarim Craton and the eastern Tianshan Orogenic Belt (NW China). The sulfide-mineralized Pobei mafic–ultramafic complex is located in the northeastern part of the Tarim Craton. The complex is composed of gabbro and olivine gabbro, cut by dunite, wehrlite, and melatroctolite of the Poyi and Poshi intrusions. Disseminated Ni–Cu sulfide mineralization is present towards the base of the ultramafic bodies. The sulfide mineralization is typically low grade (<0.5 wt.% Ni and <2 wt.% S) with low platinum-group element (PGE) concentrations (<24.5 ppb Pt and <69 ppb Pd); the abundance of Cu in 100 % sulfide is 1–8 wt.%, and Ni abundance in 100 % sulfide is typically >4 wt.%. Samples from the Pobei complex have εNd (at 280 Ma) values up to +8.1, consistent with the derivation of the magma from an asthenospheric mantle source. Fo 89.5 mol.% olivine from the ultramafic bodies is consistent with a primitive parental magma. Sulfide-bearing dunite and wehrlite have high Cu/Pd ratios ranging from 24,000 to 218,000, indicating a magma that evolved under conditions of sulfide saturation. The grades of Ni, Cu, and PGE in 100 % sulfide show a strong positive correlation. A model for these variations is proposed where the mantle source of the Pobei magma retained ~0.033 wt.% sulfide during the production of a PGE-depleted parental magma. The parental magma migrated from the mantle to the crust and underwent further S saturation to generate the observed mineralization along with its high Cu/Pd ratio at an R-factor varying from 100 to 1,200. The mineralization at Poshi and Poyi has very high γOs (at 280 Ma) values (+30 to +292) that are negatively correlated with the abundance of Os in 100 % sulfide (5.81–271 ppb) and positively correlated with the Re/Os ratios; this indicates that sulfide saturation was triggered by the assimilation of crustal sulfide with both high γOs and Re/Os ratios. When compared to other Permian mafic–ultramafic intrusions with sulfide mineralization in the East Tianshan, the Poyi and Poshi ultramafic bodies were formed from more primitive magmas, and this helps to explain why the sulfide mineralization has high Ni tenor.     

Mg---NH4 exchange on humic acid: A radiotracer technique for conditional exchange constants in a seawater medium

A radiotracer technique, employing ²⁷Mg, is used to determine the Mg released by ammonium exchange on undis-solved humic acid in a seawater medium. This new method allows for the measurement of exchangeable Mg on the solid phase surface, which eliminates the problem caused by the high-Mg background in the seawater matrix. The precision calculated from the counting statistics is better than ±2%; the reproducibility among repeated counts ranged from ±1% to ±3%. The higher sensitivity of the method allows for monitoring the Mg---NH₄ exchange at concentrations as low as 30 mM NH₄. This is a major improvement relative to the data obtained with the analytical methods used so far, which allow detection of exchangeable Mg only at NH₄ concentrations higher than 1 M. The lower experimental concentrations are more in accordance with the natural ammonium levels found in anoxic marine sediments. For the undissolved humic acid used in this experiment, the amount of exchangeable Mg in apparent equilibrium with an ammonium-free seawater matrix was found to be 96.6 ± 0.4 meq/100g. The Mg---NH₄ exchange on humic acid in seawater comes to a steady-state value in < 18 min. The conditional equilibrium constant obtained for this reaction, K_cond = 0.039 ± 0.001 M⁻¹. The technique can be expanded to other geochemical solid phases in seawater and it can be modified to study the behavior of the major cations by using ²⁴Na, ⁴²K and ⁴⁹Ca.