Macro‐and Microstructural,Textural Fabrics and Deformation Mechanism of Calcite Mylonites from Xar Moron‐Changchun Dextral Shear Zone,Northeast China

The calcite mylonites in the Xar Moron-Changchun shear zone show a significance dextral shearing characteristics. The asymmetric(σ-structure) calcite/quartz grains or aggregates, asymmetry of calcite c-axes fabric diagrams and the oblique foliation of recrystallized calcite grains correspond to a top-to-E shearing. Mineral deformation behaviors, twin morphology, C-axis EBSD fabrics, and quartz grain size-frequency diagrams demonstrate that the ductile shear zone was developed under conditions of greenschist facies, with the range of deformation temperatures from 200 to 300°C. These subgrains of host grains and surrounding recrystallized grains, strong undulose extinction, and slightly curved grain boundaries are probably results of intracrystalline deformation and dynamic recrystallization implying that the deformation took place within the dislocation-creep regime at shallow crustal levels. The calculated paleo-strain rates are between 10~(–7.87)s~(–1) and 10~(–11.49)s~(–1) with differential stresses of 32.63–63.94 MPa lying at the higher bound of typical strain rates in shear zones at crustal levels, and may indicate a relatively rapid deformation. The S-L-calcite tectonites have undergone a component of uplift which led to subhorizontal lifting in an already non-coaxial compressional deformation regime with a bulk pure shear-dominated general shear. This E-W large-scale dextral strike-slip movement is a consequence of the eastward extrusion of the Xing'an-Mongolian Orogenic Belt, and results from far-field forces associated with Late Triassic convergence domains after the final closure of the Paleo-Asian Ocean.     

Form and distribution of gold mobilized into surface waters and sediments from a gossan tailings pile,Murray Brook massive sulphide deposit,New Brunswick,Canada

Stream waters and sediments draining a gossan tailings pile at the Murray Brook massive sulphide deposit were collected to investigate Au mobility. Weathering of the massive sulphides at Murray Brook during the Late Tertiary period resulted in the concentration of Au in the gossan cap overlying the supergene Cu and unoxidized massive sulphide zones of the deposit. The gossan was mined between 1989 and 1992, and Au and Ag were extracted using a cyanide vat leach process. Although stream sediments prior to mining had Au<5 ppb (the detection limit), sediments collected in 1997 had Au contents ranging up to 256 ppm with values up to 6 ppm more than 3 km downstream from the deposit. Dissolved Au contents were similarly anomalous, up to 19 μg/L and in excess of 3 μg/L 3 km downstream. The elevated Au contents in the waters and sediments are interpreted to reflect complexation of Au (as Au(CN)₂⁻) by cyanide hosted within the gossan tailings pile. Precipitation recharges through the tailings pile with groundwater flow exiting to Gossan Creek. Degradation of cyanide along the flow path and within Gossan Creek allows colloidal Au to form via reduction of Au(I) by Fe²⁺, consistent with SEM observations of Au as <1 μm subrounded particles. In the surface waters, the majority of the Au must be in a form <0.45 μm in size to account for the similarity in Au contents between the <0.45 μm and unfiltered samples. The very elevated stream sediment Au values close to the headwaters of Gossan Creek near the tailings indicate that upon exiting to the surface environment, Au(CN)₂⁻ complexes are rapidly destroyed and Au removed from solution. However, the high Au_{<0.004 μm}/Au_total in the headwaters and the extended Au dispersion in Gossan Creek waters and sediments suggest that Au(CN)₂⁻ complexes persist for the full length of Gossan Creek. The decrease in aqueous Au which is less than 0.004 μm indicates that Au is converted from a complexed form to a colloidal form with increasing distance downstream, consistent with dissolved NO₃⁻ contents which decrease from 5210 μg/L near the headwaters to 1350 μg/L at the lower end of the stream.     

Direct characterization of airborne particles associated with arsenic-rich mine tailings: Particle size,mineralogy and texture

Windblown and vehicle-raised dust from unvegetated mine tailings can be a human health risk. Airborne particles from As-rich abandoned Au mine tailings from Nova Scotia, Canada have been characterized in terms of particle size, As concentration, As oxidation state, mineral species and texture. Samples were collected in seven aerodynamically fractionated size ranges (0.5–16 μm) using a cascade impactor deployed at three tailings fields. All three sites are used for recreational activities and off-road vehicles were racing on the tailings at two mines during sample collection. Total concentrations of As in the <8 μm fraction varied from 65 to 1040 ng/m³ of air as measured by proton-induced X-ray emission (PIXE) analysis. The same samples were analysed by synchrotron-based microfocused X-ray absorption near-edge spectroscopy (μXANES) and X-ray diffraction (μXRD) and found to contain multiple As-bearing mineral species, including Fe–As weathering products. The As species present in the dust were similar to those observed in the near-surface tailings. The action of vehicles on the tailings surface may disaggregate material cemented with Fe arsenate and contribute additional fine-grained As-rich particles to airborne dust. Results from this study can be used to help assess the potential human health risks associated with exposure to airborne particles from mine tailings.     

Experimental deformation of partially melted granitic aggregates

Abstract The effects of varying amounts of partial melt on the deformation of granitic aggregates have been tested experimentally at conditions (900°C, 1500 MPa, 10^-4 to 10^-6/s) where melt-free samples deform by dislocation creep, with microstructures approximately equivalent to those of upper greenschist facies. Experiments were performed on samples of various grain sizes, including an aplite (150 μm) and sintered aggregates of quartz-albitemicrocline (10–50 and 2–10 μm). Water was added to the samples to obtain various amounts of melt (1–15% in the aplite, 1–5% in the sintered aggregates). Optical and TEM observations of the melt distribution in hydrostatically annealed samples show that the melt in the sintered aggregates is homogeneously distributed along an interconnected network of triple junction channels, while the melt in the aplites is inhomogeneously distributed. The effect of partial melt on deformation depends an melt amount and distribution, grain size and strain rate. For samples deformed with ? 1% melt, all grain sizes exhibit microstructures indicative of dislocation creep. For samples deformed with 3–5% melt, the 150 μm and 10–50 μm grain size samples also exhibit dislocation creep microstructures, but the 2–10 μm grain size samples exhibit abundant TEM-scale evidence of dissolution-precipitation and little evidence of dislocation activity, suggesting a switch in deformation mechanism to predominantly melt-enhanced diffusion creep. At natural strain rates melt-enhanced diffusion creep would predominate at larger grain sizes, although probably not for most coarse-grained granites. The effects of melt percentage and strain rate have been studied for the 150 μm aplites. For samples with ? 5 and 10% melt, deformation at 10^–6/s squeezes excess melt out of the central compressed region allowing predominantly dislocation creep. Conversely, deformation at 10^-5/s produces considerable cataclasis presumably because the excess melt cannot flow laterally fast enough and a high pore fluid pressure results. For samples with 15% melt, deformation at both strain rates produces cataclasis, presumably because the inhomogeneous melt distribution resulted in regions of decoupled grains, which would produce high stress concentrations at point contacts. At natural strain rates there should be little or no cataclasis if an equilibrium melt texture exists and if the melt can flow as fast as the imposed strain rate. However, if the melt is confined and cannot migrate, a high pore fluid pressure should promote brittle deformation.     

Consolidation and incipient oxidation of alkaline arsenopyrite-bearing mine tailings,Macraes Mine,New Zealand

Fine grained (ca. 15 μm), arsenopyrite-bearing mine tailings have been exposed to drying and oxidation for 4 a pending relocation. The tailings are still partly covered by a pond of decanted pore waters. The water table in drying tailings has lowered by 1–3 m and desiccation cracks up to 2 cm wide have formed on the 1 m scale, extending through the unsaturated zone. Tailings in the unsaturated zone have similar pore water contents to saturated tailings: typically 16–32 wt% water. Saturated tailings retain alkaline pH (ca. 10) from the mine cyanidation plant, but pH lowers progressively towards ca. 7 near the surface, or near desiccation cracks, in the unsaturated zone. The redox state of the tailings changes in parallel with pH, with an empirical relationship: Eh(mV)=−55 pH+290. Water in the remnant decant pond reflects this relationship also. Unsaturated tailings have variable but low permeabilities, typically 10⁻³ to 10⁻⁴ m/day, and more permeable horizons have allowed incursion of oxygenated air and/or rain water from desiccation cracks. Sulphide grains in all tailings examined are unaltered. Sulphides and solutions in the tailings are out of thermodynamic equilibrium predicted from the redox–pH conditions, due to kinetic constraints. Incursion of rain water locally facilitates deposition from pore waters of insoluble Fe oxide and arsenate minerals, thus fixing As in the dry unsaturated tailings.     

Geological analogue for circumneutral pH mine tailings: implications for long-term storage,Macraes Mine,Otago, New Zealand

Tailings from the Macraes Au mine cyanidation process are stored in an impoundment about 0.6 km² and 80 m deep whose pH is maintained near 8 by the neutralizing capacity of the gangue minerals. The tailings are sandy (>50 μm particles), have a hydraulic conductivity of about 10⁻² m/day, and contain 0.1–1.0 wt.% S and 0.1–1.5 wt.% graphitic C from the primary deposit. Concentrations of As in the pore water of the mixed tailings, which are a combination of various tailings types, range from 0.1 to 20 ppm, HCO₃^- is 100 to 200 ppm, and dissolved SO₄ is 100–1700 ppm. The mixed tailings will be stored in this impoundment in perpetuity after mining ceases. Confidence in the long-term pH stability of these tailings can be gained from examination of mineralogically and chemically similar geological analogues in the immediate vicinity. A sequence, typically about 5 m thick, of sands and gravels derived from the Macraes mineralized zone 12–28 ka ago contains rounded detrital sulfide mineral grains which are unoxidized despite their close proximity to the surface and the occasional incursion of oxygenated waters. These sediments have a hydraulic conductivity of about 10⁻⁴ m/day. Saturating water pH is currently 7–8. Sands with 0.2–0.8 wt.% organic C host SO₄-reducing bacteria (SRB), and local cementation by authigenic framboidal pyrite has occurred. SRB were found in water-saturated sediments with decreased hydraulic conductivity and alkaline and anoxic conditions. These bacteria are involved in the formation of authigenic framboidal pyrite, reducing the cycling of dissolved Fe in the sediments. Carbon is not a limiting factor in this process as organic matter is present in the sandstone and ground water contains up to 180 ppm HCO₃^-. Comparison of the 28 ka old sediments with the modern tailings suggests that the chemical behaviour of the two will be similar, possibly with the crystallization of authigenic pyrite in the tailings over the long term. As long as the present slightly anoxic and circumneutral pH environmental conditions are maintained in the mixed tailings impoundment, sulfide decomposition and acidification are unlikely.     

Investigating bauxite residue flocculation by hydroxamate and polyacrylate flocculants utilising the focussed beam reflectance measurement probe

Polyacrylate and hydroxamate flocculants are commonly used to aid solid–liquid separation of bauxite residue from pregnant liquor in the Bayer process. This study presents the direct examination of the bauxite residue flocculation with polyacrylate and hydroxamate flocculants, using the focussed beam reflectance measurement (FBRM) probe to monitor aggregate dimensions.The key difference between polyacrylate and hydroxamate flocculation was found to be the way the aggregates developed post-shear, with hydroxamate flocculation exhibiting a greater degree of post-shear flocculation. Polyacrylate aggregates were found to be more dense and shear resistant, while the hydroxamate aggregates exhibited greater fines capture and lower solids in the supernatant. The solids remaining in the supernatant after flocculation were found to differ for each flocculant, with the polyacrylate system having relatively more coarse particles within the solid and the hydroxamate system being relatively finer and more iron rich. The observed results are discussed in terms of the different way in which each polymer is considered to adsorb onto the residue material.     

Formation and geochemical significance of micrometallic aggregates including fissiogenic platinum group elements in the Oklo natural reactor, Gabon

Metallic aggregates with a size of a few tens μm and consisting mainly of Ru, Rh, Pd, Te, Pb, As, Sb, S and Bi were found in the acid residue of SD37-S2/CD uraninite taken from Oklo natural reactor zone (RZ) 13. Quantitative analyses of major elements using an electron probe microanalyzer and in situ isotopic analyses of Zr, Mo, Ru, Pb and U using a sensitive high-resolution ion microprobe were performed on the metallic aggregates to determine the geochemical behaviors of fission products and actinides and to ascertain the processes of formation of the aggregates in the RZs. The chemical compositions of the aggregates investigated in this study are significantly different from those reported previously, showing lower Pb content and no correlation between the contents of Pb and S in the individual grains. The ²³⁵U/²³⁸U ratios in metallic aggregates vary significantly from 0.00478 to 0.01466, indicating chemical fractionation between U and Pu during the formation of the aggregates. The Pb isotopic data indicate that most of the Pb in the aggregates decayed from 2.05 Ga-old uraninite that existed in the RZ originally and that there was chemical fractionation between U and Pb in some aggregates. The Zr and Mo isotopic ratios, ⁹⁰Zr/⁹¹Zr and ⁹⁵Mo/⁹⁷Mo, for most of the aggregates had small variations, which can be simply explained by constant separate mixing of fissiogenic and nonfissiogenic components. On the other hand, a large variation in the ⁹⁹Ru/¹⁰¹Ru ratio (0.324-1.73) cannot be explained only by a two component mixing theory; thus, chemical fractionation between Tc and Ru during the reactor criticality is suggested. The large variations in the ²³⁵U/²³⁸U and ⁹⁹Ru/¹⁰¹Ru isotopic ratios suggest that the aggregates formed under various redox conditions owing to the radiolysis of water.     

Post-deformational annealing of calcite rocks

The evolution of microstructure and crystallographic preferred orientation (CPO) during post-deformational annealing was studied on three calcite rock types differing in purity and grain size: Carrara marble (98% calcite, mean grain size of 115 μm), Solnhofen limestone (96%, 5 μm) and synthetic calcite aggregates (99%, 7 μm). Samples were first deformed in torsion at 727 °C at a shear strain rate of 3 × 10^{− 4} s^{− 1} to a shear strain of 5 and subsequently heat-treated at 727 °C for various durations between 0 and 24 h. Microstructures and CPOs were analysed by optical microscopy, image analysis and electron backscatter diffraction (EBSD).All rock types deformed in the dislocation creep field at the same applied conditions, but their microstructures and CPOs after deformation and after annealing differed depending on starting grain size and material composition. In Carrara marble and in the synthetic calcite aggregate, a strong CPO developed during deformation accompanied by dynamic recrystallisation with significant changes in grain size. During annealing, widespread grain growth and subtle changes of CPO occurred, and equilibrated foam microstructures were approached after long annealing times. The CPO is the only feature in annealed samples indicating an earlier deformation phase, although it is not always identical to the CPO formed during deformation. In the more impure Solnhofen limestone, secondary phases on grain boundaries suppressed grain boundary mobility and prevented both the formation of a recrystallisation CPO during deformation and grain size modification during deformation and annealing.     

Distribution of arsenic and nickel in uranium mill tailings,Rabbit Lake,Saskatchewan, Canada

The Rabbit Lake U mine in-pit tailings management facility (TMF) is located in northern Saskatchewan, Canada. The tailings body is approximately 425 m long×300 m wide and 91 m thick at its centre. An investigation of the TMF was performed to collect tailings samples from depth to quantify the distribution of As and Ni in the tailings with respect to ore type and assess the distribution of As and Ni with respect to tailings mineralogy. The tailings body consists of alternating layers of ice, frozen tailings and unfrozen tailings which varied in texture from a slurry to a firm silty sand. The tailings solids are predominately composed of quartz (16–36%), calcium sulphate (0.3–54%) and illite (3 and 14%). Arsenic and Ni concentrations in the tailings show similar patterns with depth which were strongly related to historical changes in As and Ni concentrations in the mill feed. Mineralogy of the ore bodies indicated that As and Ni in the mill feed occurred primarily as 1:1 molar ratio arsenides such as niccolite and gersdorffite. Arsenic and Ni concentrations in the tailings were also measured at a near 1:1 molar ratio. Mill process records showed that an average of 71% of the As in the mill feed was solubilized during leaching. SEM analysis suggested that solubilized As is precipitated as Ca²⁺, Fe³⁺ and Ni²⁺ arsenates during the neutralization process. Mill records indicated that 17,000 tonnes of As were discharged to the TMF of which approximately 88% was as arsenates and 12% as primary arsenides.     

Geotechnical Characteristics of Copper Mine Tailings: A Case Study

Waste management issue in mining industry has become increasingly important. In this regard, construction of tailings dams plays a major role. Most of the tailings dams require some kinds of remedial actions during their operational lifetime, among which heightening is the most common. In the first stage of the remedial provisions for Sarcheshmeh Copper Complex tailings dam in Iran, it has been decided to use hydrocyclone method to provide suitable construction material due to the high cost associated with using borrow materials for heightening of the dam. To undertake this project a series of laboratory experiments was performed to determine the copper ‘original tailings’ and ‘cycloned materials’ geotechnical characteristics to evaluate the applicability of the cycloned materials for construction purposes. Different laboratory experiments were conducted to determine the grain-size distribution, Atterberg limits, specific gravity, maximum density, shear strength parameters, consolidation coefficient, and hydraulic conductivity. The results were compared with those of similar mines to check whether they follow the trends observed in other copper tailing materials elsewhere. Variation of the cohesion and internal friction angle versus different compaction ratios were studied in order to determine realistic shear strength parameters for tailing dam stability analysis. In this study, using oedometer test, a mild linear relation between void ratio and the consolidation coefficient has been found for tailings materials. By considering the effects of void ratio and weight of passing sieve #200 materials, a new relationship is proposed that can be used for estimating the copper slimes hydraulic conductivity in seepage analysis of tailings dams.     

Biomass and productivity of three phytoplankton size classes in San Francisco Bay

Primary productivity of three size classes of phytoplankton (<5 μm, 5–22 μm, >22 μm) was measured monthly at six sites within San Francisco Bay throughout 1980. These sites in the three principal embayments were chosen to represent a range of environments, phytoplankton communities, and seasonal cycles in the estuary. Temporal variations in productivity for each size class generaly followed the seasonality of the corresponding fraction of phytoplankton biomass. The 5–22 μm size class accounted for 40 to 50% of the annual production in each embayment, but production by phytoplankton >22 μm ranged from 26% in the southern reach to 54% of total phytoplankton production in the landward embayment of the northern reach. A productivity index is derived that predicts daily productivity for each size class as a function of ambient irradiance and integrated chlorophylla in the photic zone. For the whole phytoplankton community and for each size class, this index was constant and estimated as ?0.76 g C m^?2 (g chlorophylla Einstein)^?1. The annual means of maximum carbon assimilation numbers were usually similar for the three size classes. Spatial and temporal variations in size-fractionated productivity are shown to be primarily due to differences in biomass rather than size-dependent carbon assimilation rates. *** DIRECT SUPPORT *** A01BY034 00005     

Heavy metal contamination of soils and waters in and around the Imcheon Au–Ag mine,Korea

The heavy metal contamination of soils and waters by metalliferous mining activities in an area of Korea was studied. In the study area of the Imcheon Au–Ag mine, soils and waters were sampled and analyzed using AAS for Cd, Cu, Pb and Zn. Analysis of HCO₃⁻, F⁻, NO₃⁻ and SO₄²⁻ in water samples was also undertaken by ion chromatography. Elevated concentrations of the metals were found in tailings. The maximum contents in the tailings were 9.4, 229, 6160 and 1640 mg/kg extracted by aqua regia and 1.35, 26.4, 70.3 and 410 mg/kg extracted by 0.1 N HCl solution for Cd, Cu, Pb and Zn, respectively. These metals are continuously dispersed downstream and downslope from the tailings by clastic movement through wind and water. Because of the existence of sulfides in the tailings, a water sample taken on the tailings site was very acidic with a pH of 2.2, with high total dissolved solids (TDS) of 1845 mg/l and electric conductivity (EC) of 3820 μS/cm. This sample also contained up to 0.27, 1.90, 2.80, 53.4, 4,700 mg/l of Cd, Cu, Pb, Zn and SO₄²⁻, respectively. TDS, EC and concentrations of metals in waters decreased with distance from the tailings. The total amount of pulverized limestone needed for neutralizing the acid tailings was estimated to be 46 metric tons, assuming its volume of 45,000 m³ and its bulk density of 1855 kg/m³.     

Sintering of olivine and olivine-basalt aggregates

The sintering behavior of olivine and olivine-basalt aggregates has been examined at temperatures near 1,300° C. Experimental factors contributing to rapid sintering kinetics and high-density, fine-grained specimens include: (i) the uniform dispersion of basalt throughout the specimen, (ii) a very fine, uniform particle size for the olivine powder, (iii) oxygen fugacities near the high P _O2 end of the olivine stability field, and (iv) rapid heating to the sintering temperature. Olivine-basalt specimens prepared from olivine particles coated with a synthetic basalt achieve chemical and microstructural equilibrium more rapidly, as well as produce higher density and finer grain-sized aggregates, than do specimens prepared by mechanical mixing of olivine and natural basalt powders. The grain boundary mobility for olivine, measured for olivine-basalt aggregates which have undergone secondary recrystallization, is on the order of 2×10^?15 (m/s)/(N/m²) in the temperature range 1,300–1,400° C. Solution-precipitation (pressure-solution) processes make an important contribution to the development of the microstructure in olivine-basalt aggregates.     

Dependence of radon exhalation on grain size of sedimentary waste

Tailings resulted from sulphuric acid leaching process of uranium from sedimentary rocks contain high concentrations of ²²⁶Ra and its daughters, the most important of which is ²²²Rn. Movement of radon gas out of the tailings is strongly influenced by the physicochemical characteristics of these tailings especially their radium content and the grain size. So, the tailing samples were size fractionated into four sizes (>?250, 250–125, 125–74 and <?74 µm). The natural radioactivity was investigated using hyper-pure germanium detector and solid-state nuclear track detectors (CR-39) for bulk size and after size fractionation. The activity concentrations of different radionuclides in size-fractionated tailing samples have been shown to be strongly dependent on the size of the particles. In the range of >?250 and <?74 µm, the activity concentrations of ²³⁰Th, ²²⁶Ra, ²¹⁴Pb, ²¹⁴Bi, ²¹⁰Pb, ²³²Th and ⁴⁰K increased throughout with decreasing particle size, while that of ²³⁸U, ²³⁴U and ²³⁵U have an opposite effect. The results revealed an inverse relationship between the radon exhalation rate and size fractionation. Also, the results showed a good correlation between radium activity concentration and radon mass exhalation rate.     

Distribution, characterization, and geochemical controls of elements of concern in uranium mine tailings, Key Lake, Saskatchewan, Canada

The distribution of As, Mo, Ni and Se in the aqueous and solid phases of U mine tailings in the Deilmann Tailings Management Facility (DTMF), located at the Key Lake mine in northern Saskatchewan, Canada, was defined using as-discharged tailings samples collected monthly starting in 1996 and core samples collected from the DTMF from 3 locations on 3 occasions between 2004 and 2009. These data indicated that the DTMF can be divided into two geochemical zones; tailings generated from the Deilmann ore body between 1996 and 2000 and tailings from the McArthur River ore body, mined after July 2000. The Deilmann tailings solids are generally characterized by greater elemental concentrations than those in the McArthur River tailings, particularly for As, Co and Ni. These elevated concentrations are attributed to the abundance of Ni–Co–As–S minerals in this ore. The mean aqueous concentrations of As, Mo, Ni, and Se are 3.7, 23.2, 0.14, and 0.02 mg L⁻¹, respectively, in the Deilmann porewaters and 0.20, 4.16, 0.06, and 0.03 mg L⁻¹, respectively, in the McArthur River porewaters. Similarly, the mean As, Mo, Ni, and Se solid phase concentrations are 5.89 × 10³, 69.9, 3.20 × 10³, and 17.4 μg g⁻¹, respectively, for the Deilmann tailings and 440, 13.6, 551, and 3.03 μg g⁻¹ in the McArthur River tailings. Statistically, pH remained unchanged from the time of discharge while Eh values have remained oxic with no significant change between the two tailings types over 15 a of residence time. Results from sequential extractions, thermodynamic modeling, and results of complimentary research indicated that ferrihydrite solubility is the dominant control on aqueous As concentrations and also plays a role in controlling dissolved Mo, Ni and Se.     

Transport properties of olivine grain boundaries from electrical conductivity experiments

Grain boundary processes contribute significantly to electronic and ionic transports in materials within Earth’s interior. We report a novel experimental study of grain boundary conductivity in highly strained olivine aggregates that demonstrates the importance of misorientation angle between adjacent grains on aggregate transport properties. We performed electrical conductivity measurements of melt-free polycrystalline olivine (Fo₉₀) samples that had been previously deformed at 1200 °C and 0.3 GPa to shear strains up to γ?=?7.3. The electrical conductivity and anisotropy were measured at 2.8 GPa over the temperature range 700–1400 °C. We observed that (1) the electrical conductivity of samples with a small grain size (3–6 µm) and strong crystallographic preferred orientation produced by dynamic recrystallization during large-strain shear deformation is a factor of 10 or more larger than that measured on coarse-grained samples, (2) the sample deformed to the highest strain is the most conductive even though it does not have the smallest grain size, and (3) conductivity is up to a factor of ~?4 larger in the direction of shear than normal to the shear plane. Based on these results combined with electrical conductivity data for coarse-grained, polycrystalline olivine and for single crystals, we propose that the electrical conductivity of our fine-grained samples is dominated by grain boundary paths. In addition, the electrical anisotropy results from preferential alignment of higher-conductivity grain boundaries associated with the development of a strong crystallographic preferred orientation of the grains.     

Development of fluid conduits in the auriferous shear zones of the Hutti Gold Mine, India: evidence for spatially and temporally heterogeneous fluid flow

The gold mineralization of the Hutti Mine is hosted by nine parallel, N–S trending, steeply dipping, 2–10 m wide shear zones, that transect Archaean amphibolites. The shear zones were formed after peak metamorphism during retrograde ductile D₂ shearing in the lower amphibolite facies. They were reactivated in the lower to mid greenschist facies by brittle–ductile D₃ shearing and intense quartz veining. The development of a S₂–S₃ crenulation cleavage facilitates the discrimination between the two deformation events and contemporaneous alteration and gold mineralization. Ductile D₂ shearing is associated with a pervasively developed distal chlorite–sericite alteration assemblage in the outer parts of the shear zones and the proximal biotite–plagioclase alteration in the center of the shear zones. D₃ is characterized by development of the inner chlorite-K-feldspar alteration, which forms a centimeter-scale alteration halo surrounding the laminated quartz veins and replaces earlier biotite along S₃. The average size of the laminated vein systems is 30–50 m along strike as well as down-dip and 2–6 m in width.Mass balance calculations suggest strong metasomatic changes for the proximal biotite–plagioclase alteration yielding mass and volume increase of ca. 16% and 12%, respectively. The calculated mass and volume changes of the distal chlorite–sericite alteration (ca. 11%, ca. 8%) are lower. The decrease in δ¹⁸O values of the whole rock from around 7.5‰ for the host rocks to 6–7‰ for the distal chlorite–sericite and the proximal biotite–plagioclase alteration and around 5‰ for the inner chlorite-K-feldspar alteration suggests hydrothermal alteration during two-stage deformation and fluid flow.The ductile D₂ deformation in the lower amphibolite facies has provided grain scale porosities by microfracturing. The pervasive, steady-state fluid flow resulted in a disseminated style of gold–sulfide mineralization and a penetrative alteration of the host rocks. Alternating ductile and brittle D₃ deformation during lower to mid greenschist facies conditions followed the fault-valve process. Ductile creep in the shear zones resulted in a low permeability environment leading to fluid pressure build-up. Strongly episodic fluid advection and mass transfer was controlled by repeated seismic fracturing during the formation of laminated quartz(-gold) veins. The limitation of quartz veins to the extent of earlier shear zones indicate the importance of pre-existing anisotropies for fault-valve action and economic gold mineralization.     

Weakening and strain localization produced by syn-deformational reaction of plagioclase

There are many observations in naturally deformed rocks on the effects of mineral reactions on deformation, but few experimental data. In order to study the effects of chemical disequilibrium on deformation we have investigated the hydration reaction plagioclase + H₂OM more albitic plagioclase + zoisite + kyanite + quartz. We utilized fine-grained (2-6 µm) plagioclase aggregates of two compositions (An54 and An60), both dried and with 0.1-0.4 wt% H₂O present, in shear deformation experiments at two sets of conditions: 900 °C, 1.0 GPa (in the plagioclase stability field) and 750 °C, 1.5 GPa (in the zoisite stability field). Dry samples and those deformed in the plagioclase stability field underwent homogeneous shearing by dislocation creep, but samples with 0.1 to 0.4 wt% water deformed in the zoisite stability field showed extreme strain localization into very narrow (~1-3 µm) shear bands after low shear strain. In these samples the microstructures of reaction products in the matrix differ from those in the shear bands. In the matrix, large (up to 400 µm) zoisite crystals grew in the direction of finite extension, and relict plagioclase grains are surrounded by rims of recrystallized grains that are more albitic. In the shear bands, the reaction products albitic plagioclase, zoisite, white mica, and traces of kyanite form polyphase aggregates of very fine-grained (<0.1 µm) dislocation-free grains. Most of the sample strain after % ~2 has occurred within the shear bands, within which the dominant deformation mechanism is inferred to be diffusion-accommodated grain boundary sliding (DAGBS). The switch from dislocation creep in dry samples deformed without reaction to DAGBS in reacted samples is associated with a decrease in flow stress from ~800 to <200 MPa. These experiments demonstrate that heterogeneous nucleation driven in part by chemical disequilibrium can produce an extremely fine-grained polyphase assemblage, leading to a switch in deformation mechanism and significant weakening. Thus, localization of deformation in polyphase rocks may occur on any pressure (P),temperature (T)-path where the equilibrium composition of the constituent minerals changes.     

Characterisation of the Sarcheshmeh copper mine tailings,Kerman province,southeast of Iran

Mineral processing operation at the Sarcheshmeh porphyry copper mine has produced huge quantities of tailings materials containing sulphide minerals in particular pyrite. These tailings materials were geochemically and mineralogically characterised to assess pyrite and chalcopyrite oxidation, acid mine drainage generation, and trace element mobility to lead development of a proper remediation plan. Five vertical trenches up to 4.2 m deep were excavated from the tailings surface, and 70 solid samples were taken in 0.3 m intervals. The samples were first mineralogically analysed. Pyrite was the main sulphide mineral found in the tailings. The gangue minerals include quartz ± muscovite–illite ± chlorite ± albite ± orthoclase ± halite. The samples were geochemically analysed for total concentrations of 62 elements, paste pH, SO₄ ^2?, CO₃ ^2?, and HCO₃ ^?. The maximum concentrations of SO₄ ^2? (1,300, 1,170, 1,852, 1,960 and 837 mg/L) were observed at a depth of 0.9 m in profiles A, B, C, D and E, respectively. The tailings have a high acid-producing potential and low acid-neutralising potential (pyrite 4–6 wt %, calcite 1 wt %). Fe₂(SO₄)₃, CuSO₄, MgSO₄ and MnSO₄ were the dominant secondary sulphate minerals in the tailings. The lowest pH values (2.9, 3 and 3) were measured at a depth of 0.3 m in the profiles A, B and C, 3.9 at a depth of 0.6 m in the profile D and 3 at a depth of 0.9 m in the profile E. The upper portions of the profiles C (1.8 m) and D (2.1 m) were moderately oxidised, while oxidation in the profiles A, B and E did not extend more than 1.2, 1.2 and 1.5 m beneath the tailings surface. Zn, Pb, Rb, U, Hf, Nd, Zr and Ga show almost a constant trend with depth. Cd, Sr, Th, La and Ce increased with increasing depth of the tailings materials while, Co, V, Ti, Cr, Cu, As, Mn, Ag, Mo and Ni exhibit initially a decreasing trend from tailings surface to the depths that vary between 0.9 and 1.2. They then remained constant with the depth. The results show pyrite and chalcopyrite oxidation at surface layers of the tailings and subsequent leaching of the oxidation products and trace elements by infiltrated atmospheric precipitation.