Surface chemical mechanisms of inadvertent recovery of chromite in UG2 ore flotation: Residual layer identification using statistical ToF-SIMS analysis

In the UG2 ore (Bushveld Complex, South Africa) flotation, normally more than 3% of the gangue minerals, principally chromite with talc and pyroxene, report to the concentrate diluting the PGM recovery and contributing to subsequent processing costs. Previous studies have identified residual talc-like layers on orthopyroxene surfaces in Merensky ore flotation contributing to inadvertent flotation of relatively large particles (20–150 µm) of this mineral. Chromite (75–150 µm) from flotation of UG2 ore has been similarly examined. Statistical comparison of ToF-SIMS analysis of particles from concentrate and tails reveals no significant difference in Cu, Pb, Ni and collector (IBX and DTP) signals between these streams but surface exposure of Mg and Si is favoured in the concentrate. The flotation rate of coarse chromite correlates with the exposures of magnesium and silicon in patches on the chromite surface; higher exposures give earlier flotation. Conversely, there is a negative correlation with signals corresponding to the chromite surface, i.e. Cr, Fe, Al. Flotation of chromite without collector has confirmed this statistical discrimination. Hydrophobic talc-like residual layers, similar to those found on orthopyroxene surfaces, probably from partial alteration, explain this flotation mechanism.     

Flotation kinetics of a pyritic gold ore

Kinetics of semi-batch flotation behavior of a gold ore from North-Western Quebec, Canada was investigated with respect to fineness of grind (P₈₀). The gold was mostly associated with pyrite in native form as inclusions and was also in contact with pyrite along the boundaries of non-sulphide gangue. Gold recoveries were found to increase from 91.8% to 95.8% as the particles size decreased from an F₈₀ of 205 μm to 53 μm. Data treatment according to the graphical method of kinetic analysis indicated a much better fit to second order kinetics for both gold and pyrite with correlation coefficients higher than 0.998 compared to first order kinetics with correlation coefficients of less than 0.95. Variation and implication of flotation rate constants are discussed with respect to chemical conditions and particle size.     

Metal and arsenic distribution in soil particle sizes relevant to soil ingestion by children

Ingestion of soil is a common behaviour in young children as a means of exploring their surroundings. Much attention has been given to remediation of point-source polluted sites with regard to potential health risks for children. However, because of diffuse pollution and long-range atmospheric deposition, soil contaminant levels are generally increased in urban areas compared to their rural counterparts, even in areas located away from any point sources of pollution. Intake of urban soil can thereby result in significant amounts of the child’s daily metal intake. In the present study, soil samples were collected from 25 playgrounds around urban Uppsala, Sweden and analysed for contents of Al, As, Fe, Cr, Cu, Cd, Hg, Mn, Ni, Pb, W and Zn. Prior to aqua regia digestion, the samples were wet-sieved in order to separate soil particle fractions representing deliberate (<4 mm) and involuntary (<50 μm) soil ingestion by children, as well as a third size fraction of 50–100 μm representing soil that is easily transported by suspension. While the metal and As contents in the 50–100 μm fraction were similar to those of the <4 mm fraction, the <50 μm fraction had metal and As contents on average one and a half times higher than those of the <4 mm fraction. The metal and As contents correlated negatively with the sand content in both particle size fractions <4 mm and 50–100 μm, suggesting a general decrease in metal and As content with increasing sand content. However, a positive correlation was found between sand content and the metal and As contents of the finest fraction (<50 μm), suggesting that when the sand content is high, the bulk of the sorbed elements are on the finest particles. The difference between metal and As contents in the different size fractions was greater in the soil sample with the highest sand content than in the sample with the lowest sand content. This implies that texture is a significant factor in metal and As distribution in soils with moderate metal and As contents, when the number of binding sites associated with small particles is low. Tolerable daily intake (TDI) values for Pb and As were exceeded at all sites, and at two sites for Cd, for children with pica behaviour. A high ingestion rate of mainly small particles could also result in the TDI value for Pb being exceeded at 10 sites and that for As at one site. This study also found that soil analysis by the procedure recommended by Swedish authorities accurately represents the metal intake from deliberate soil ingestion, whereas involuntary soil ingestion of mainly small particles could result in metal intakes which are up to twice as high.     

Characterisation of sphalerite and pyrite flotation samples by XPS and ToF-SIMS

The surface analytical techniques of X-ray Photoelectron Spectroscopy (XPS) and Time of Flight Secondary Ion Mass Spectroscopy (ToF-SIMS) have provided information on the type and concentration of species on the surface of sphalerite and pyrite particles in flotation concentrate and tail samples, but also on their distribution on each particle and across particles of different sizes. From this surface analytical study, a more accurate interpretation of the flotation results of sphalerite and pyrite minerals in a mixed mineral system could be made as a function of the concentrations of copper sulphate activator and xanthate collector, and particle size. In particular, it was found that sphalerite particles reporting to the concentrate are larger in size and contain less iron hydroxide on their surface than particles reporting to the tail. As for the pyrite particles, their lower recovery than the sphalerite particles is the result of a larger proportion of iron hydroxide on their surface inhibiting copper and collector adsorption.     

Is silt the most influential soil grain size fraction?

The contribution of individual grain size fractions (2000–500, 500–250, 250–63, 63–2 and < 2 μm) to bulk soil surface area and reactivity is discussed with reference to mineralogical and oxalate and dithionite extractions data. The 63–2 μm fraction contributed up to 56% and 67% of bulk soil volume and BET surface area, respectively. Consideration of these observations and the mineralogy of this fraction suggest that the 63–2 μm fraction may be the most influential for the release of elements via mineral dissolution in the bulk soil.     

Rheology of aqueous magnetite suspensions in uniform magnetic fields

Non-magnetized suspensions of magnetite particles with concentrations in excess of 30% by mass and particle size less than 75 μm exhibit Bingham plastic behaviour. When exposed to external magnetic fields of strengths in excess of 41 × 10⁻⁴ T, the rheological behaviour of the suspensions departs from the Bingham model and can be described by a Herschel–Bulkley model of the form τ = τ₀ + kγⁿ. The value of the index n was found to range from 0.38 to 0.9, depending on the magnetic field strength, solids concentration and particle size and correlations are proposed for the apparent viscosity of magnetized suspensions as a function of magnetic field strength and solids concentration.     

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.     

Biometry of the Late Cretaceous Arkhangelskiella group: ecophenotypes controlled by nutrient flux

This study focuses on the morphometry and taxonomy of the Late Cretaceous coccolith genus Arkhangelskiella. Sixty samples from the Campanian–Maastrichtian interval of DSDP Hole 390A (Blake Nose) were investigated for their contents of Arkhangelskiella spp. In each sample one hundred specimens of Arkhangelskiella spp. were examined by measuring the coccolith length and width, as well as the length and width of the central area. In the samples investigated the Arkhangelskiella group exhibits a large size variation, specimens length varies from 4.95 μm to 14.52 μm. Former taxonomic concepts, based on morphometry, subdivided the Arkhangelskiella group into three species: Arkhangelskiella maastrichtiana, Arkhangelskiella confusa and Arkhangelskiella cymbiformis. Our data show a large variability of the morphometric data (coccolith length, width of the outer rim). There is no indication for three independant species; two of the quoted taxa (1. thick outer rim = Arkhangelskiella maastrichtiana; 2. very thin outer rim = Arkkhangelskiella cymbiformis) seem to be extreme forms of a continuous morphometric lineage. The lower part of the investigated succession (139.92–133.42 mbsf) is dominated by small specimens with an average length of 6.8 μm whereas the upper part (132.86–126.15 mbsf) is characterized by larger specimens (mean 8.7 μm). In DSDP Hole 390A the size increase appears to be very abrupt, within two samples (samples 133.42 mbsf, 132.86 mbsf) the mean size increases by 1.51 μm. Previous morphometric studies of Arkhangelskiella indicate a more continuous size increase throughout the late Campanian–Maastrichtian. The abrupt size increase observed here hints toward a minor hiatus in DSDP Hole 390A separating upper Campanian from lower Maastrichtian sediments. It seems likely that the size increase of Arkhangelskiella reflects changes of various environmental factors like nutrient supply and sea water chemistry (Mg/Ca ratio; Ca concentration). A comparison of morphometric results with previous palaeoecological studies documents a nutrient control for the growth of Arkhangelskiella. Small specimens can be related to more mesotrophic conditions whereas large specimens are linked to oligotrophic surface waters.     

Re–Os dating of chalcopyrite from selected mineral deposits in the Kalatag district in the eastern Tianshan Orogen,China

The Kalatag Cu–Zn–Au district contains a number of economically important Cu deposits in eastern Tianshan in Xinjiang, NW China. Due to the lack of precise mineralization ages, the metallogenesis of this area has long been a matter of debate. In this study, chalcopyrite Re–Os isotope methods are used to date the South Meiling Cu–Zn and Hongshi Cu deposits in the eastern part of Kalatag area.The South Meiling Cu–Zn deposit is hosted in volcanic-sedimentary rocks of the Late Ordovician to Early Silurian Daliugou Formation. The deposit consists of two parts: a concordant massive sulfide ores and discordant vein-type ores located in the footwall strata. The principal ore minerals are pyrite, chalcopyrite, sphalerite, minor tetrahedrite, galena and pyrrhotite. Gangue minerals include quartz, sericite and barite, and minor chlorite, plagioclase and carbonate minerals. The Hongshi Cu deposit represents a hydrothermal vein system hosted in the mafic volcanic rocks of Daliugou Formation. The orebodies are associated with quartz veins and controlled by subsidiary faults of the Kalatag fault. The ore-forming process can be divided into the early, middle and late stages and is characterized by quartz–pyrite, quartz–chalcopyrite–pyrite and quartz–carbonate–gypsum veins, respectively.Re–Os analyses of chalcopyrite from the South Meiling Cu–Zn deposit yield an isochron age of 434.2 ± 3.9 Ma and initial ¹⁸⁷Os/¹⁸⁸Os ratio of 0.647 ± 0.098 (MSWD = 0.59). Re–Os analyses of chalcopyrite from the Hongshi Cu deposit yield an isochron age of 431.8 ± 2.7 Ma and initial ¹⁸⁷Os/¹⁸⁸Os ratio of − 0.165 ± 0.075 (MSWD = 0.77). Since chalcopyrite is the primary copper mineral, we interpret these isochron ages as the timing of Cu mineralization, based on field geology and petrographic evidence. These results suggest that the Re–Os ages presented here provide, for the first time, a direct constraint on an early Paleozoic Cu mineralization event of the eastern Tianshan Orogen. The high initial ¹⁸⁷Os/¹⁸⁸Os ratios (0.647 ± 0.098) ratio of ~ 434 Ma chalcopyrite from the South Meiling deposit suggest that the metal was sourced from a two end-member mixing of crust and mantle materials. Moreover, we propose that the VMS mineral system and hydrothermal vein system of the Kalatag district were related to the south-dipping subduction of the Kalamaili oceanic plate during the Late Ordovician–Silurian.     

Native antimony in the Baogutu gold deposit (west Junggar,NW China): Its occurrence and origin

The Baogutu gold deposit, West Junggar (Xinjiang, NW China), is composed of quartz–sulfide veins and their stockworks and is hosted within an Early Carboniferous volcanic–sedimentary sequence. Three ore-forming paragenetic stages can be identified: coarse-grained quartz–sulfide vein (stage I), gold-bearing fine-grained quartz–sulfide vein (stage II), and native antimony-bearing calcite–sulfide veinlets (stage III). The estimated formation temperatures (approximately 360 to 220 °C), fS₂ (? 7 to ? 15 log units), and fO₂ (? 26 to ? 43 log units) decrease from stage I, through stage II, to stage III. The nature of the hydrothermal fluid changed from weakly acidic (pH: 5 to 6 at stage I) to alkaline (pH: > 7 at stage III).Two different occurrences of native antimony could be identified: one coexists with chalcopyrite and pyrrhotite, whereas the other occurs as isolate grains within calcite veins. Native antimony (up to 100 μm in size) contains minor amounts of As (2.0 to 2.7 wt.%); empirical formula Sb_0.95–0.96As_0.03–0.04. Decrease of temperature and fO₂ at high pH and low fS₂ conditions favored co-precipitation of native antimony–ullmannite assemblages and the decomposition of tetrahedrite. Native antimony crystallized later than the native gold, suggesting fractionation between Au and Sb during the hydrothermal evolution of the deposit.     

Surface potential and dixanthogen stability on chalcopyrite surface

Contact angle measurements, ultraviolet (UV) spectroscopy and voltammetry were used in this investigation to study the effect of various externally applied potentials on the stability of dixanthogen at synthetic and natural chalcopyrite surfaces.The results of contact angle measurements indicate that synthetic and natural chalcopyrites have similar wettabilities. Their hydrophobic potential range in a 7 × 10^− 4 M PAX solution was + 0.04 V to + 0.44 V vs. NHE at pH 10 and was − 0.01 V to + 0.54 V at pH 7.UV spectroscopic results show that dixanthogen began to form on the chalcopyrite surface at a potential of + 0.04 V vs. NHE at pH 10 and − 0.01 V vs. NHE at pH 7. The amount of dixanthogen formed on the chalcopyrite surface initially increased with the increase of the applied potential and then decreased with the increasing potential. The optimum potential range for dixanthogen formation on the chalcopyrite surface was from + 0.14 V to + 0.34 V vs. NHE at pH 10 and from + 0.14 V to + 0.44 V vs. NHE at pH 7. It was difficult to completely remove the dixanthogen film on the chalcopyrite surface.     

Chemical and K–Ar systematics of a mylonitic mica after natural and experimental interactions with varied fluids

Flow-through and batch-leaching experiments combining mineralogical, chemical and K–Ar isotopic analyses of mica separates from a mylonitic sample of the Tyndrum faulting system in Scotland (U.K.) were conducted to evaluate and simulate the natural interaction with H₂SO₄-loaded river water at pHs of 3–4. The flow-through experiments with H₂SO₄-loaded and pure deionized water completed by a batch-leaching experiment with 1 M HCl at room temperature had varied effects on soluble mineral phases, such as Fe-sulfates and Ca/Mg-carbonates, that were present in the varied mica size fractions, but none caused the mineralogical and K–Ar characteristics of the mica to differ from separates of the natural environment.Despite the limited number of K–Ar ages, size fractionation of the mylonitic mica identified two generations of mica with different REE patterns. The coarser (2–8 μm) fraction yielded a high La/Yb ratio of 4.3 and crystallized at 359 ± 6 Ma at a temperature of 250–300 °C, probably during a major tectonic-thermal activity. The smaller (< 0.5 μm) fraction yielded a La/Yb ratio of 2.1, a younger K–Ar age at 315 ± 5 Ma and a lower crystallization temperature of about 200 °C.     

The use of water-extractable Cu,Mo, Zn,As, Pb concentrations and automated mineral analysis of flue dust particles as tools for impact studies in topsoils exposed to past emissions of a Cu-smelter

An exploratory study has been conducted to test the utility of automated mineral analysis observations to identify flue dust particles in topsoils exposed for several decades to emissions of a copper smelter. The methods used are readily available in mining countries. To identify the most impacted sites, the Cu, Zn, Pb, Mo and As levels in water and diluted sulphuric acid extractions of four topsoil size fractions (833–495 μm, 246–148 μm; 74–38 μm; <38 μm) were analysed. X-ray diffraction analyses were used to demonstrate the mineralogical degradation of smectite phases when approaching the smelter. Flue dust particles in different states of conservation in topsoils were directly observed by scanning electron microscopy (SEM) aided by energy dispersive detection of X-rays. Qemscan^® scanning of dispersed topsoil preparations (10,000 particles) pinpoints smelter particles by their density; flue dust pearls can be tracked by sorting particles according to their sphericity, clearly identifying them as pyrometallurgical products. When sorting soil particles by mineral groups (e.g. sulphides), an increase in this phase group can be observed when approaching the smelter. SEM resolution limits observations to particles larger than 2–3 μm. Smaller particles can be observed by transmission electron microscopy, although observer experience and the availability of equipment time are essential as is the case for SEM.     

Geochemistry,mineralogy and genesis of the Ayazmant Fe–Cu skarn deposit in Ayvalik, (Balikesir), Turkey

The Ayazmant Fe–Cu skarn deposit is located approximately 20 km SE of Ayval?k or 140 km N of Izmir in western Turkey. The skarn occurs at the contact between metapelites and the metabasites of the Early Triassic K?n?k Formation and the porphyritic hypabyssal intrusive rocks of the Late Oligocene Kozak Intrusive Complex. The major, trace, and rare earth-element geochemical analysis of the igneous rocks indicate that they are I-type, subalkaline, calc-alkaline, metaluminous, I-type products of a high-level magma chamber, generated in a continental arc setting. The ⁴⁰Ar–³⁹Ar isochron age obtained from biotite of hornfels is 20.3 ± 0.1 Ma, probably reflecting the age of metamorphic–bimetasomatic alteration which commenced shortly after intrusion into impure carbonates. Three stages of skarn formation and ore development are recognized: (1) Early skarn stage (Stage I) consisting mainly of garnet with grossular-rich (Gr_75–79) cores and andradite-rich (Gr_36–38) rims, diopside (Di_94–97), scapolite and magnetite; (2) sulfide-rich skarn (Stage II), dominated by chalcopyrite with magnetite, andraditic garnet (Ad₈₄–₈₉), diopside (Di₆₅–₇₅) and actinolite; and (3) retrograde alteration (Stage III) dominated by actinolite, epidote, orthoclase, phlogopite and chlorite in which sulfides are the main ore phases. ⁴⁰Ar–³⁹Ar age data indicate that potassic alteration, synchronous or postdating magnetite–pyroxene–amphibole skarn, occurred at 20.0 ± 0.1 Ma. The high pyroxene/garnet ratio, plus the presence of scapolite in calc-silicate and associated ore paragenesis characterized by magnetite (± hematite), chalcopyrite and bornite, suggests that the bulk of the Ayazmant skarns were formed under oxidized conditions. Oxygen isotope compositions of pyroxene, magnetite and garnet of prograde skarn alteration indicate a magmatic fluid with δ¹⁸O values between 5.4 and 9.5‰. On the basis of oxygen isotope data from mineral pairs, the early stage of prograde skarn formation is characterized by pyroxene (Di_94–97)-magnetite assemblage formed at an upper temperature limit of 576 °C. The lower temperature limit for magnetite precipitation is estimated below 300 °C, on the basis of magnetite–calcite pairs either as fracture-fillings or massive ore in recrystallized limestone-marble. The sulfide assemblage is dominated by chalcopyrite with subordinate molybdenite, pyrite, cubanite, bornite, pyrrhotite, galena, sphalerite and idaite. Gold–copper mineralization formed adjacent to andradite-dominated skarn which occurs in close proximity to the intrusion contacts. Native gold and electrum are most abundant in sulfides, as fine-grained inclusions; grain size with varying from 5 to 20 µm. Sulfur isotope compositions obtained from pyrrhotite, pyrite, chalcopyrite, sphalerite and galena form a narrow range between ? 4.8 and 1.6‰, suggesting the sulfur was probably mantle-derived or leached from magmatic rocks. Geochemical data from Ayazmant shows that Cu is strongly associated with Au, Bi, Te, Se, Cd, Zn, Pb, Ni and Co. The Ayazmant mineralizing system possesses all the ingredients of a skarn system either cogenetic with, or formed prior to a porphyry Cu(Au–Mo) system. The results of this study indicate that the Aegean Region of Turkey has considerable exploration potential for both porphyry-related skarns and porphyry Cu and Au mineralization.     

Tracking magmatic and hydrothermal Nb–Ta–W–Sn fractionation using mineral textures and composition: A case study from the late Cretaceous Jiepailing ore district in the Nanling Range in South China

The Jiepailing mining district in the Nanling range in South China is well-known for its granite-related Sn–Be–F-mineralization. Recently, drill holes have exposed an Nb–Ta–W–Sn mineralized granitic porphyry and topaz-bearing granite–greisen at depth, which we have studied here, using mineral (columbite, rutile, wolframite, cassiterite, zircon, and mica) major- and trace-element compositional data, mineral textures, and zircon and columbite U–Pb geochronology. Our age data shows that the porphyry and the granite and their mineralization formed at ~ 91–89 ± 1 Ma in the late-Cretaceous, and thus subsequent to the main ore-forming events of the region. Continuous mineral compositional trends indicate that the studied granitoids are related by progressive fractionation. We propose that: (1) subhedral–euhedral, low-Ta columbite crystallized from melt; (2) euhedral–subhedral rutile and wolframite and subhedral and subhedral cassiterite up to ~ 30 μm in size formed at the magmatic–hydrothermal transition of the system; and (3) high-Ta columbite and subhedral cassiterite up to ~ 10 μm in size formed from subsolidus hydrothermal fluids. In combination with the Nb, Ta, W, and Sn compositions of zircon and mica, their textures and compositional variation allow us to track the magmatic to hydrothermal rare-metal fractionation (concentration, mobilization, and deposition) of the system in detail, despite our limited access to it through only two exploration drill cores. Using the Nb, Ta, W, and Sn concentrations in zircon (refractory, early-crystallized) and in micas (late equilibrated), respectively, was particularly useful for tracing the partial loss of Sn and W ore components from the intrusion, and to constrain the information which is crucial for any rigorous ore exploration.     

Floatability of rare earth phosphors from waste fluorescent lamps

Zeta-potential measurements were made to determine the electric state of phosphor materials on the basis of which a feasibility study could be performed for the use of flotation in the recovery of fine (d₅₀ < 13 μm) rare earth phosphors from waste fluorescent lamps. Tests were carried out with pure specimens of white (calcium halo-phosphate), red, green and blue (rare earth) phosphors, with a 17 : 1 : 1 : 1 ratio of their mixture, and with actual waste phosphor materials. The effects of a cationic (dodecyl ammonium acetate, DAA) and two anionic (sodium dodecyl sulfate (SDS) and sodium oleate (NaOl)) collectors on the floatability of materials, as well as that of Na₂SiO₃ dispersant on the separation characteristics, were investigated at different pH ranges. The process, applied to actual discarded waste phosphors gave, in a two-stage separation scheme, sink products assaying 17.7–23.8% and 21.5–25.9% rare earth phosphors for DAA and SDS flotation, respectively. The recovery and Newton's efficiency were about 70–90% and 0.26–0.37, 66–82% and 0.18–0.20, respectively for DAA and SDS flotation.     

Characteristics of modern atmospheric dust deposition in snow in the Mt. Yulong region,southeastern Tibetan Plateau

We evaluated the concentration, size and distribution, and temporal variation of insoluble dust micro-particles in the snow, rainfall and water taken from the areas surrounding the Mt. Yulong to define the characteristics of modern atmospheric dust deposition and the contributions of different dust sources. The mean mass concentration (4511 μg kg⁻¹) of micro-particles with 0.57 < d < 26 μm, and the diameter (11.5 μm) of dust contained in the water bodies of the Mt. Yulong are roughly similar to those observed in other sites, implying that dust is primarily supplied through short-range transport from proximal source regions (several or hundreds of km distances). The mean mass concentrations of micro-particles with 0.57 < d < 26 μm is lower in the rainfall than in the snow and the river water, suggesting the rain water is an ideal source/carrier for detecting the characteristics of modern atmospheric micro-particles. Volume size distributions of micro-particles in the snow and water showed single modal structures having volume median diameters from 3 to 26 μm. Number concentrations of micro-particles in the snow were higher than that in the rainfall, the river water contains the least amount of micro-particles. Vertical profiles of the snowpits show that there is a strong lateral correlation among the dust peaks, indicating a regional uniformity of dust deposition and suitability of snow analysis for dust deposition. In addition, the bare rock of snow-free terrain in the Mt. Yulong region and the mineral particles from local rock weathering are also important sources for the dust deposition.     

Ion microprobe U–Th–Pb geochronology and study of micro-inclusions in zircon from the Himalayan high- and ultrahigh-pressure eclogites,Kaghan Valley of Pakistan

We report ion microprobe U–Th–Pb geochronology of in situ zircon from the Himalayan high- and ultrahigh-pressure eclogites, Kaghan Valley of Pakistan. Combined with the textural features, mineral inclusions, cathodoluminescence image information and the U–Th–Pb isotope geochronology, two types of zircons were recognized in Group I and II eclogites. Zircons in Group I eclogites are of considerably large size (>100 μm up to 500 μm). A few grains are euhederal and prismatic, show oscillatory zoning with distinct core–rim luminescence pattern. Several other grains show irregular morphology, mitamictization, embayment and boundary truncations. They contain micro-inclusions such as muscovite, biotite, quartz and albite. Core or middle portions of zircons from Group I eclogites yielded concordant U–Th–Pb age of 267.6 ± 2.4 Ma (MSWD = 8.5), have higher U and Th contents with a Th/U ratio > 1, indicating typical magmatic core domains. Middle and rim or outer portions of these zircons contain inclusions of garnet, omphacite, phengite and these portions show no clear zonation. They yielded discordant values ranging between 210 and 71 Ma, indicating several thermal or Pb-loss events during their growth and recrystalization prior to or during the Himalayan eclogite-facies metamorphism. Zircons in Group II eclogites are smaller in size, prismatic to oval, display patchy or sector zoning and contain abundant inclusions of garnet, omphacite, phengite, quartz, rutile and carbonates. They yielded concordant U–Th–Pb age of 44.9 ± 1.2 Ma (MSWD = 4.9). The lower U and Th contents and a lower Th/U ratio (<0.05) in these zircons suggest their formation from the recrystallization of the older zircons during the Himalayan high and ultrahigh-pressure eclogite-facies metamorphism.     

The genesis of metal zonation in the Weilasituo and Bairendaba Ag–Zn–Pb–Cu–(Sn–W) deposits in the shallow part of a porphyry Sn–W–Rb system,Inner Mongolia,China

The Weilasituo and Bairendaba Zn–Pb–Ag–Cu–(Sn–W) sulphide deposits are located in the southern part of Great Xing'an Range of Inner Mongolia in China. The deposits are located at shallow depths in the newly discovered Weilasituo porphyry hosting Sn–W–Rb mineralization. The mineralization at Weilasituo and Bairendaba consist of zoned massive sulphide veins within fractures cutting the Xilinhot Metamorphic Complex and quartz diorite. The Weilasituo deposit gradually zones from the Cu-rich Zn–Cu sulphide mineralization in the west to Zn-rich Zn–Cu sulphide mineralization in the east. The Bairendaba deposit has a Cu-bearing and Zn-rich core through a transitional zone devoid of copper to an outer zone of Zn–Pb–Ag mineralization. Three main veins contain more than 50 wt.% of the contained metal in the two deposits with their metal ratios displaying a systematic and gradual increase in Zn/Cu, Pb/Zn and Ag/Zn ratios from the western part of Weilasituo to the eastern part of Bairendaba.Three stages of vein-type mineralization are recognized. Early, sub-economic mineralization consists of a variable proportion of euhedral arsenopyrite, pyrite, quartz, and rare wolframite, scheelite, cassiterite, magnetite and cobaltite. This was succeeded by main stage mineralization with economic concentration of zoned Cu, Zn, Pb and Ag sulphide minerals along strike within the veins. The zones consist of the assemblages: (1) pyrrhotite–Fe-rich sphalerite–chalcopyrite(–quartz–fluorite) at west Weilasituo; (2) pyrrhotite–Fe-rich sphalerite–chalcopyrite(–galena–tetrahedrite–quartz–fluorite) at east Weilasituo; (3) pyrrhotite–Fe-rich sphalerite–chalcopyrite(–galena–tetrahedrite–quartz–fluorite) in the centre of Bairendaba; (4) pyrrhotite–Fe-rich sphalerite–galena(–chalcopyrite–tetrahedrite–quartz–fluorite) in the transition zone of Bairendaba; and (5) pyrrhotite–Fe-rich sphalerite–galena–tetrahedrite(–chalcopyrite–falkmanite–argentite–pyrargyrite–quartz–fluorite) in the outer zone at Bairendaba. Post-main ore stage is devoid of sulphides and characterized overprinting of fluorite, sericite, chlorite, illite, kaolinite and calcite.Zircon SHRIMP U–Pb dating, Zircon LA–ICP–MS U–Pb dating, molybdenite Re–Os isochron dating, and muscovite Ar–Ar dating indicate the Beidashan granitic batholith was intruded at 140 ± 3 Ma (MSWD = 3.3), the porphyritic monzogranite from marginal facies of the Beidashan batholith was intruded at 139 ± 2 Ma (MSWD = 0.75), the mineralized quartz porphyry was intruded at 135 ± 2 Ma (MSWD = 0.91), the greisen mineralization occurred at 135 ± 11 Ma (MSWD = 7.2), and the post-main ore stage muscovite deposited at 129.5 ± 0.9 Ma. The new geochronology data show the porphyry Sn–W–Rb and vein-type sulphide mineralization are contemporaneous with granitic magmatism in the region.The metal zonation at the Weilasituo and Bairendaba deposits is a result of progressive metal deposition. This was during the evolution of a metal-bearing fluid along the strike of the veins and during the main stage of ore formation at the upper part of the deep-seated porphyry Sn–W–Rb system. This progressive zonation indicates that the deposits represent end-numbers formed from one ore-forming fluid, which moved from west to east from the porphyry. The metal zonation patterns of the major veins are consistent with metal-bearing fluid entering the system with the precipitation of chalcopyrite proximally and sphalerite, galena and Ag-bearing minerals more distally. We show that the mechanism of metal deposition is therefore controlled by thermodynamic conditions resulting in the progressive separation of sulphides from the metal-bearing fluid. The temperature gradient between the inflow zone and the outflow zone appears to be one of the key parameters controlling the formation of the metal zonation pattern. The sulphide precipitation sequence is consistent with a low fS₂ and low fO₂ state of the acidic metal-bearing fluid. The metal zonation pattern provides helpful clues from which it is possible to establish the nature of fluid migration and metal deposition models to locate a possible porphyry mineralization at depth in the Great Xing'an Range, which is consistent with the geology of the newly discovered porphyry Sn–W–Rb system.     

The nature and distribution of Cu,Zn, Hg,and Pb in urban soils of a regional city: Lithgow,Australia

This study investigates the concentration and spatial distribution of Cu, Zn, Hg and Pb in the surface (0–2 cm) soils of a regional city in Australia. Surface soils were collected from road sides and analysed for their total Cu, Zn, Hg and Pb concentrations in the <180 μm and <2 mm grain size fractions. The average metal concentration of surface soils, relative to local background soils at 40–50 cm depth, are twice as enriched in Hg, more than three times enriched in Cu and Zn, and nearly six times as enriched in Pb. Median surface soil metal concentration values were Cu – 39 mg/kg (682 mg/kg max), Zn – 120 mg/kg (4950 mg/kg max), Hg – 44 μg/kg (14,900 μg/kg max) and Pb – 46 mg/kg (3490 mg/kg max). Five sites exceeded the Australian NEPC (1999) 300 mg/kg guideline for Pb in residential soils. Strong positive correlations between Cu, Zn and Pb, coupled with the spatial distribution of elevated soil concentrations towards the city centre and main roads suggest traffic and older housing as major sources of contamination. No spatial relationships were identified between elevated metal loadings and locations of past or present industries.