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1.
Adsorption onto Fe-containing minerals is a well-known remediation method for As-contaminated water and soil. In this study, the use of acid mine drainage sludge (AMDS) to adsorb As was investigated. AMDS is composed of amorphous particles and so has a large surface area (251.2 m2 g−1). Here, adsorption of both arsenite and arsenate was found to be almost 100%, under various initial AMDS dosages, with the arsenate adsorption rate being faster. The optimum pH for As adsorption onto AMDS was pH 7.0 and the maximum adsorption capacities for arsenite and arsenate were 58.5 mg g−1 and 19.7 mg g−1 AMDS, respectively. In addition, experiments revealed that AMDS dosages decreased As release from contaminated soil. Therefore, the AMDS used in this study was confirmed to be a suitable candidate for immobilizing both arsenite and arsenate in contaminated soils. 相似文献
2.
《Applied Geochemistry》2006,21(10):1760-1780
Sulfide-rich mine tailings in Adak that are exposed to weathering cause acid mine drainage characterized by low pH (2–4) and high SO4 (up to 800 mg L−1). Surface water, sediment and soil samples collected in this study contain higher concentrations of As, Cu, Fe and Zn, compared to the target and/or intervention limits set by international regulatory agencies. In particular, high As concentrations in water (up to 2900 μg L−1) and sediment (up to 900 mg kg−1) are of concern. There is large variability in trace element concentrations, implying that both physical (grain size) and chemical factors (pH, secondary phases as sulfides, Al-oxides or clay minerals) play an important role in their distribution. The low pH keeps the trace elements dissolved, and they are transported farther downstream. Trace element partition coefficients are low (log Kd = 0.3–4.3), and saturation indices calculated with PHREEQC are <0 for common oxide and sulfidic minerals. The sediment and soil samples indicate an enhanced pollution index (up to 17), and high enrichment factors for trace elements (As up to 38,300; Zn up to 800). Finally, leaves collected from different plant types indicate bioaccumulation of several elements (As, Al, Cu, Fe and Zn). However, some of the plants growing in this area (e.g., Salix, Equisétum) are generally resistant to metal toxicity, and hence, liming and phytoremediation could be considered as potential on-site remediation methods. 相似文献
3.
《Applied Geochemistry》2006,21(9):1522-1538
Factors controlling the chemical composition of water interacting with finely-crushed kimberlite have been investigated by sampling pore waters from processed kimberlite fines stored in a containment facility. Discharge water from the diamond recovery plant and surface water from the containment facility, which acts as plant intake water, were also sampled. All waters sampled are pH-neutral, enriched in SO4, Mg, Ca, and K, and low in Fe. Pore-water samples, representing the most concentrated waters, are characterized by the highest SO4 (up to 4080 mg l−1), Mg (up to 870 mg l−1), and Ca (up to 473 mg l−1). The water discharged from the processing plant has higher concentrations of all major dissolved constituents than the intake water. The dominant minerals present in the processed fines and the kimberlite ore are serpentine and olivine, with small amounts of Ca sulphate and Fe sulphide restricted to mud xenoclasts. Reaction and inverse modeling suggest that much of the water-rock interaction takes place within the plant and involves the dissolution of chrysotile and Ca sulphate, and precipitation of silica and Mg carbonate. Evapoconcentration also appears to be a significant process affecting pore water composition in the containment facility. The reaction proposed to be occurring during ore processing involves the dissolution of CO2(g) and may represent an opportunity to sequester atmospheric CO2 through mineral carbonation. 相似文献
4.
Titratable actual acidity (TAA) is a technique commonly used to estimate the existing pool of exchangeable H+ in acid sulfate soils (ASS). A widely adopted version of the TAA method involves titrating a 1M KCl suspension of oven-dry soil (1:40) with NaOH to a known pH endpoint. However, when ASS are subject to long term re-flooding during wetland remediation, former sulfuric horizons can develop substantial quantities of porewater Fe2+, non-sulfidic solid-phase Fe(II) and a variety of reduced inorganic sulfur (RIS) species (e.g. pyrite, mackinawite, greigite and elemental sulfur). For these sediments, an oven-drying approach may induce oxidation of the abundant Fe(II) and/or reactive RIS species, thereby generating H+ and leading to overestimation of existing in situ exchangeable H+. In this study, we compare TAA via the standard approach (1M KCl; 1:40; oven-dry soil, 4 hr extract; TAAD) with an identical O2-free extraction approach using wet-sediment (TAAW). We apply both methods to former sulfuric horizon sediments from freshwater re-flooded ASS wetlands. There are significant (α = 0.01) differences (up to 12×) between TAA measured by the two methods, with the oven-dried standard approach overestimating TAA relative to the wet, O2-free approach in 85% of cases. Despite the fact that all AVS-S and some S(0) was oxidised during the oven-drying process, the increases in TAA (TAAD–TAAW) show very weak correlation(s) with corresponding losses in RIS species or increases in water soluble sulfate and KCl extractable sulfate. However, oven-drying caused substantial loss of 1M KCl exchangeable Fe(II) and 1 M HCl-extractable Fe(II) and led to large increases in 1 M HCl-extractable Fe(III). These changes in Fe fractions displayed strong positive linear correlation (α = 0.01) with increases in TAA. Although this is not evidence of causality, it suggests that oxidation of Fe(II) species are playing an important role in the development of additional exchangeable H+ and may be largely responsible for the contrasting TAA derived by the two methods. The differences in TAA between the two methods are greatest in organic-rich surface sediments and are significantly positively correlated with total organic carbon content. These findings have major implications for accurately assessing TAA in re-flooded ASS wetlands. 相似文献
5.
This study seeks to quantify the rate and timing of regolith generation in the Critical Zone at the Susquehanna Shale Hills Critical Zone Observatory (SSHO). Meteoric 10Be depth profiles were determined using measurements from 30 hillslope soil and bedrock core samples in an effort to constrain 10Be inventories. The SSHO is located in the temperate climate zone of central Pennsylvania and comprises a first-order watershed developed entirely on a Fe-rich, organic-poor, Silurian-aged shale. Two major perturbations to the landscape have occurred at SSHO in the geologically recent past, including significant and sustained periglacial activity until after the retreat of the Laurentide ice sheet (～21 ka) and deforestation during early colonial land-use. Bulk soil samples (n = 16) were collected at three locations along a planar hillslope on the southern ridge of the catchment, representing the ridge top, mid-slope and valley floor. Rock chip samples (n = 14) were also collected from a 24 m deep core drilled into the northern ridge top. All meteoric 10Be concentration profiles show a declining trend with depth, with most of the 10Be retained in the uppermost decimeters of the soil. Meteoric 10Be inventories are higher at the mid-slope and valley floor sample sites, at 3.71 ± 0.02 × 1010 at/cm2 and 3.69 ± 0.02 × 1010 at/cm2, than at the ridge top site (1.90 ± 0.01 × 1010 at/cm2). The 10Be inventory at the convex ridge top site implies a minimum residence time of ～10.6 ka, or if erosion is steady, an erosion rate of 19.4 ± 0.2 m/My. 相似文献
6.
Rapid weathering and erosion rates in mountainous tropical watersheds lead to highly variable soil and saprolite thicknesses which in turn impact nutrient fluxes and biological populations. In the Luquillo Mountains of Puerto Rico, a 5-m thick saprolite contains high microorganism densities at the surface and at depth overlying bedrock. We test the hypotheses that the organisms at depth are limited by the availability of two nutrients, P and Fe. Many tropical soils are P-limited, rather than N-limited, and dissolution of apatite is the dominant source of P. We document patterns of apatite weathering and of bioavailable Fe derived from the weathering of primary minerals hornblende and biotite in cores augered to 7.5 m on a ridgetop as compared to spheroidally weathering bedrock sampled in a nearby roadcut.Iron isotopic compositions of 0.5 N HCl extracts of soil and saprolite range from about δ56Fe = 0 to ? 0.1‰ throughout the saprolite except at the surface and at 5 m depth where δ56Fe = ? 0.26 to ? 0.64‰. The enrichment of light isotopes in HCl-extractable Fe in the soil and at the saprolite–bedrock interface is consistent with active Fe cycling and consistent with the locations of high cell densities and Fe(II)-oxidizing bacteria, identified previously. To evaluate the potential P-limitation of Fe-cycling bacteria in the profile, solid-state concentrations of P were measured as a function of depth in the soil, saprolite, and weathering bedrock. Weathering apatite crystals were examined in thin sections and an apatite dissolution rate of 6.8 × 10? 14 mol m? 2 s? 1 was calculated. While surface communities depend on recycled nutrients and atmospheric inputs, deep communities survive primarily on nutrients released by the weathering bedrock and thus are tightly coupled to processes related to saprolite formation including mineral weathering. While low available P may limit microbial activity within the middle saprolite, fluxes of P from apatite weathering should be sufficient to support robust growth of microorganisms in the deep saprolite. 相似文献
7.
《Chemie der Erde / Geochemistry》2015,75(2):261-270
The aim of this study was to investigate the accumulation of arsenic (As) in and on roots of Zea mays (maize) and Helianthus annuus (sunflower) by means of synchrotron-based micro-focused X-ray fluorescence imaging (μ-XRF). Plant and soil samples were collected from two field sites in the Hetao Plain (Inner Mongolia, China) which have been regularly irrigated with As-rich groundwater. Detailed μ-XRF element distribution maps were generated at the Fluo-beamline of the Anka synchrotron facility (Karlsruhe Institute of Technology) to assess the spatial distribution of As in thin sections of plant roots and soil particles. The results showed that average As concentrations in the roots (14.5–27.4 mg kg−1) covered a similar range as in the surrounding soil, but local maximum root As concentrations reached up to 424 mg kg−1 (H. annuus) and 1280 mg kg−1 (Z. mays), respectively. Importantly, the results revealed that As had mainly accumulated at the outer rhizodermis along with iron (Fe). We therefore conclude that thin crusts of Fe-(hydr)oxides cover the roots and act as an effective barrier to As, similar to the formation of Fe plaque in rice roots. In contrast to permanently flooded rice paddy fields, regular flood irrigation results in variable redox conditions within the silty and loamy soils at our study site and fosters the formation of Fe-(hydr)oxide plaque on the root surfaces. 相似文献
8.
The original ore-fluid of the Huogeqi Cu–Pb–Zn deposit in Inner Mongolia, northern China, was enriched in heavy oxygen isotopes with δ18O values ranging from 9.9 to 11.4 per mil, which is characteristic of the metamorphic devolatilization of pelitic rocks. The δD values determined by direct measurement of syn-ore hydrothermal tremolite range from − 116 to − 82 per mil, lying between the domains of typical metamorphic fluid and meteoric water, which is in equilibrium with organic matter. Oxygen and hydrogen isotope ratios indicate that the ore-fluid was derived from deep-sourced metamorphic fluid and interacted with organic-rich shale during fluid migration, which is consistent with the fluid evolution history revealed by a previous fluid inclusion study. Sulfides in the deposit are characteristically enriched in heavy S isotopes, with an average δ34S value of 13.4 ± 6.2 per mil (1σ, n = 103). The S-isotope ratios are identical to stratabound sulfides generated through the non-bacterial reduction of Neoproterozoic marine sulfate (with δ34S values of ~ 17 per mil). Previous studies on lead isotopes of sulfides revealed that the ore-forming metals (Cu, Pb, and Zn) at the Huogeqi deposit were also remobilized from a stratabound source. This source was syngenetically elevated in its Cu-, Pb-, and Zn-sulfide content as a result of submarine hydrothermal activities forming sulfide-rich layers within a rift tectonic setting. The Fe isotope ratios for sulfides are consistent with those of an intercalated iron-formation within the ore-hosting rocks, suggesting that the Fe in the sulfides was derived from local host rocks during sulfide precipitation and the Fe-rich rocks are favorable lithological units for high-grade mineralization. The heterogeneous sources of ore-fluid, S, ore-forming metals, and Fe are explained by a multistage genetic model, which is supported by the geological characteristic of the deposit. The enriched sulfides were subsequently remobilized and enriched by metamorphic devolatilization during the Permian and Triassic periods. The metamorphic ore-fluid ascended along a shear zone and interacted with organic-rich shale. Sulfides eventually precipitated within the shear zone at a shallower crustal level, especially where the shear zone intersected Fe-rich host rocks. This multistage genetic model has implications for mineral exploration. Greenschist to amphibolite facies terranes containing thick Neoproterozoic rift sequences are ideal regions for potential Cu–Pb–Zn mineralization. In particular, intercalated volcanic rocks within the rift sequences are indicative of high heat-flow and are ideal for the development of submarine hydrothermal systems. The primary structures hosting mineralization and ore shoots in the Huogeqi area are jogs in the shear zones. In addition, Fe-rich lithological units, such as iron-formations, are ideal hosts for high-grade ore. 相似文献
9.
Copper and iron skarn deposits are economically important types of skarn deposits throughout the world, especially in China, but the differences between Cu and Fe skarn deposits are poorly constrained. The Edong ore district in southeastern Hubei Province, Middle–Lower Yangtze River metallogenic belt, China, contains numerous Fe and Cu–Fe skarn deposits. In this contribution, variations in skarn mineralogy, mineralization-related intrusions and sulfur isotope values between these Cu–Fe and Fe skarn deposits are discussed.The garnets and pyroxenes of the Cu–Fe and Fe skarn deposits in the Edong ore district share similar compositions, i.e., dominantly andradite (Ad29–100Gr0–68) and diopside (Di54–100Hd0–38), respectively. This feature indicates that the mineral compositions of skarn silicate mineral assemblages were not the critical controlling factors for variations between the Cu–Fe and Fe skarn deposits. Intrusions associated with skarn Fe deposits in the Edong ore district differ from those Cu–Fe skarn deposits in petrology, geochemistry and Sr–Nd isotope. Intrusions associated with Fe deposits have large variations in their (La/Yb)N ratios (3.84–24.6) and Eu anomalies (δEu = 0.32–1.65), and have relatively low Sr/Y ratios (4.2–44.0) and high Yb contents (1.20–11.8 ppm), as well as radiogenic Sr–Nd isotopes (εNd(t) = − 12.5 to − 9.2) and (87Sr/86Sr)i = 0.7067 to 0.7086. In contrast, intrusions associated with Cu–Fe deposits are characterized by relatively high Sr/Y (35.0–81.3) and (La/Yb)N (15.0–31.6) ratios, low Yb contents (1.00–1.62 ppm) without obvious Eu anomalies (δEu = 0.67–0.97), as well as (87Sr/86Sr)i = 0.7055 to 0.7068 and εNd(t) = − 7.9 to − 3.4. Geochemical evidence indicates a greater contribution from the crust in intrusions associated with Fe skarn deposits than in intrusions associated with Cu–Fe skarn deposits. In the Edong ore district, the sulfides and sulfates in the Cu–Fe skarn deposits have sulfur isotope signatures that differ from those of Fe skarn deposits. The Cu–Fe skarn deposits have a narrow range of δ34S values from − 6.2‰ to + 8.7‰ in sulfides, and + 13.2‰ to + 15.2‰ in anhydrite, while the Fe skarn deposits have a wide range of δ34S values from + 10.3‰ to + 20.0‰ in pyrite and + 18.9‰ to + 30.8‰ in anhydrite. Sulfur isotope data for anhydrite and sedimentary country rocks suggest that the formation of skarns in the Edong district involved the interaction between magmatic fluids and variable amounts of evaporites in host rocks. 相似文献
10.
《Chemie der Erde / Geochemistry》2015,75(3):345-356
The old Senhora das Fontes uranium mine, in central Portugal, consists of quartz veins which penetrated along fracture shear zones at the contact between graphite schist and orthogneiss. The mine was exploited underground until a depth of 90 m and was closed down in 1971. The ores from this mine and two others were treated in the mine area by the heap-leach process which ended in 1982. Seven dumps containing a total of about 33,800 m3 of material and partially covered by natural vegetation were left in the mine area. A remediation process took place from May 2010 to January 2011. The material deposited in dumps was relocated and covered with erosion resisting covers. Surface water and groundwater were collected in the wet season just before the remediation, in the following season at the beginning of the remediation and also after the remediation in the following dry season. Before, at the beginning and after the remediation, surface water and groundwater have an acid-to-alkaline pH, which decreased with the remediation, whereas Eh increased. In general, before the remediation, uranium concentration was up to 83 μg/L in surface water and up to 116 μg/L in groundwater, whereas at the beginning of the remediation it increases up to 183 μg/L and 272 μg/L in the former and the latter, respectively, due to the remobilization of mine dumps and pyrite and chalcopyrite exposures, responsible for the pH decrease. In general, after the remediation, the U concentration decreased significantly in surface water and groundwater at the north part of the mine area, but increased in both, particularly in the latter up to 774 μg/L in the south and southwest parts of this area, attributed to the remobilization of sulphides that caused mobilization of metals and arsenic which migrated to the groundwater flow. Uranium is adsorbed in clay minerals, but also in goethite as indicated by the geochemical modelling. After the remediation, the saturation indices of oxyhydroxides decrease as pH decreases. The remediation also caused decrease in Cd, Co, Cr, Ni, Pb, Zn, Cu, As, Sr and Mn concentrations of surface water and groundwater, particularly in the north part of the mine area, which is supported by the speciation modelling that shows the decrease of most dissolved bivalent species. However, in general, after the remediation, Th, Cd, Al, Li, Pb, Sr and As concentrations increased in groundwater and surface water at south and southwest of the mine area. Before and after the remediation, surface water and groundwater are contaminated in U, Cd, Cr, Al, Mn, Ni, Pb, Cu and As. Remediation caused only some improvement at north of the mine area, because at south and southwest part, after the remediation, the groundwater is more contaminated than before the remediation. 相似文献
11.
Serpentinite rocks, high in Mg and trace elements including Ni, Cr, Cd, Co, Cu, and Mn and low in nutrients such as Ca, K, and P, form serpentine soils with similar chemical properties resulting in chemically extreme environments for the biota that grow upon them. The impact of parent material on soil characteristics is most important in young soils, and therefore the incipient weathering of serpentinite rock likely has a strong effect on the development of serpentine soils and ecosystems. Additionally, porosity generation is a crucial process in converting rock into a soil that can support vegetation. Here, the important factors affecting the incipient weathering of serpentinite rock are examined at two sites in the Klamath Mountains, California. Serpentinite-derived soils and serpentinite rock cores were collected in depth profiles from each sampling location. Mineral dissolution in weathered serpentinite samples, determined by scanning electron microscopy, energy dispersive spectrometry, electron microprobe analyses, and synchrotron microXRD, is consistent with the order, from most weathered to least weathered: Fe-rich pyroxene > antigorite > Mg-rich lizardite > Al-rich lizardite. These results suggest that the initial porosity formation within serpentinite rock, impacting the formation of serpentine soil on which vegetation can exist, is strongly affected both by the presence of non-serpentine primary minerals as well as the composition of the serpentine minerals. In particular, the presence of ferrous Fe appears to contribute to greater dissolution, whereas the presence of Al within the parent rock appears to contribute to greater stability. Iron-oxidizing bacteria present at the soil–rock interface have been shown in previous studies to contribute to the transition from rock to soil, and soils and rock cores in this study were therefore tested for iron-oxidizing bacteria. The detection of biological iron oxidation in this study indicates that the early alteration of these Fe-rich minerals may be mediated by iron-oxidizing bacteria. These findings help provide insight into the incipient processes affecting serpentinite rock weathering, important to the development of extreme serpentine soils and the biota that grow on them. 相似文献
12.
Previous research has shown that Cu and Fe isotopes are fractionated by dissolution and precipitation reactions driven by changing redox conditions. In this study, Cu isotope composition (65Cu/63Cu ratios) was studied in profiles through sulphide-bearing tailings at the former Cu mine at Laver and in a pilot-scale test cell at the Kristineberg mine, both in northern Sweden. The profile at Kristineberg was also analysed for Fe isotope composition (56Fe/54Fe ratios). At both sites sulphide oxidation resulted in an enrichment of the lighter Cu isotope in the oxidised zone of the tailings compared to the original isotope ratio, probably due to preferential losses of the heavier Cu isotope into the liquid phase during oxidation of sulphides. In a zone with secondary enrichment of Cu, located just below the oxidation front at Laver, δ65Cu (compared to ERM-AE633) was as low as −4.35 ± 0.02‰, which can be compared to the original value of 1.31 ± 0.03‰ in the unoxidised tailings. Precipitation of covellite in the secondary Cu enrichment zone explains this fractionation. The Fe isotopic composition in the Kristineberg profile is similar in the oxidised zone and in the unoxidised zone, with average δ56Fe values (relative to the IRMM-014) of −0.58 ± 0.06‰ and −0.49 ± 0.05‰, respectively. At the well-defined oxidation front, δ56Fe was less negative, −0.24 ± 0.01‰. Processes such as Fe(II)–Fe(III) equilibrium and precipitation of Fe-(oxy)hydroxides at the oxidation front are assumed to cause this Fe isotope fractionation. This field study provides additional support for the importance of redox processes for the isotopic composition of Cu and Fe in natural systems. 相似文献
13.
In this study, we investigated Fe and Li isotope fractionation between mineral separates of olivine pheno- and xenocrysts (including one clinopyroxyene phenocryst) and their basaltic hosts. Samples were collected from the Canary Islands (Teneriffa, La Palma) and some German volcanic regions (Vogelsberg, Westerwald and Hegau). All investigated bulk samples fall in a tight range of Li and Fe isotope compositions (δ56Fewr = 0.06–0.17‰ and δ7Lima = 2.5–5.2‰, assuming δ7Li of the olivine-free matrix is virtually identical to that of the bulk sample for mass balance reasons). In contrast, olivine phenocrysts display highly variable, but generally light Fe and mostly light Li isotope compositions compared to their respective olivine-free basaltic matrix, which was considered to represent the melt (with δ56Feol = ? 0.24 to 0.14‰ and δ7Liol = ? 10.5 to + 6.5‰, respectively). Single olivine crystals from one sample display even a larger range of δ56Feol between ? 0.7 and + 0.1‰. One single clinopyroxene phenocryst displays the lightest Li isotope composition (δ7Licpx = ? 17.7‰), but no Fe isotope fractionation relative to melt. The olivine phenocrysts show variable Mg# and Ni (correlated in most cases) that range between 0.89 and 0.74 and between 300 and 3000 μg/g, respectively. These olivines likely grew by fractional crystallization in an evolving magma. One sample from the Vogelsberg volcano contained olivine xenocrysts (Mg# > 0.89 and Ni > 3000 μg/g), in addition to olivine phenocrysts. This sample displays the highest Li- and the second highest Fe-isotope fractionation between olivine and melt (Δ7Liol-melt = ? 13; Δ56Feol-melt = ? 0.29).Our data, i.e. the variable olivine- at constant whole rock and matrix isotope compositions, strongly indicate disequilibrium, i.e. kinetic Fe and Li isotope fractionation between olivine and melt (for Li also between cpx and melt) during fractional crystallization. Δ7Liol-melt is correlated with the Li partitioning between olivine and melt (i.e. with Liol/Limelt), indicating Li isotope fractionation due to preferential (faster) diffusion of 6Li into olivine during fractional crystallization. Olivine with low Δ7Liol-melt, also have low Δ56Feol-melt, indicating that Fe isotope fractionation is also driven by diffusion of isotopically light Fe into olivine, potentially, as Fe–Mg inter-diffusion. The lowest Δ56Feol-melt (? 0.40) was observed in a sample from Westerwald (Germany) with abundant magnetite, indicating relatively oxidizing conditions during magma differentiation. This may have enhanced equilibrium Fe isotope fractionation between olivine and melt or fine dispersed magnetite in the basalt matrix may have shifted its Fe isotope composition towards higher δ56Fe. The decoupling of Li- and Fe isotope fractionation in cpx is likely due to faster diffusion of Li relative to Fe in cpx, implying that the large investigated cpx phenocryst resided in the magma for only a short period of time which was sufficient for Li- but not for Fe diffusion. The absence of any equilibrium Fe isotope fractionation between the investigated cpx phenocryst and its basaltic host may be related to the similar Fe3 +/Fe2 + of cpx and melt. In contrast to cpx, the generally light Fe isotope composition of all investigated olivine separates implies the existence of equilibrium- (in addition to diffusion-driven) isotope fractionation between olivine and melt, on the order of 0.1‰. 相似文献
14.
《Lithos》2007,93(1-2):175-198
The Neoproterozoic (∼ 820 Ma) Aries micaceous kimberlite intrudes the central Kimberley Basin, northern Western Australia, and has yielded a suite of 27 serpentinised ultramafic xenoliths, including spinel-bearing and rare, metasomatised, phlogopite–biotite and rutile-bearing types, along with minor granite xenoliths. Proton-microprobe trace-element analysis of pyrope and chromian spinel grains derived from heavy mineral concentrates from the kimberlite has been used to define a ∼ 35–40 mW/m2 Proterozoic geotherm for the central Kimberley Craton. Lherzolitic chromian pyrope highly depleted in Zr and Y, and Cr-rich magnesiochromite xenocrysts (class 1), probably were derived from depleted garnet peridotite mantle at ∼ 150 km depth. Sampling of shallower levels of the lithospheric mantle by kimberlite magmas in the north and north-extension lobes entrained high-Fe chromite xenocrysts (class 2), and aluminous spinel-bearing xenoliths, where both spinel compositions are anomalously Fe-rich for spinels from mantle xenoliths. This Fe-enrichment may have resulted from Fe–Mg exchange with olivine during slow cooling of the peridotite host rocks. Fine exsolution rods of aluminous spinel in diopside and zircon in rutile grains in spinel- and rutile-bearing serpentinised ultramafic xenoliths, respectively, suggest nearly isobaric cooling of host rocks in the lithospheric mantle, and indicate that at least some aluminous spinel in spinel-facies peridotites formed through exsolution from chromian diopside. Fe–Ti-rich metasomatism in the spinel-facies Kimberley mantle probably produced high-Ti phlogopite–biotite + rutile and Ti, V, Zn, Ni-enriched aluminous spinel ± ilmenite associations in several ultramafic xenoliths. U–Pb SHRIMP 207Pb/206Pb zircon ages for one granite (1851 ± 10 Ma) and two serpentinised ultramafic xenoliths (1845 ± 30 Ma; 1861 ± 31 Ma) indicate that the granitic basement and lower crust beneath the central Kimberley Basin are at least Palaeoproterozoic in age. However, Hf-isotope analyses of the zircons in the ultramafic xenoliths suggest that the underlying lithospheric mantle is at least late Archean in age. 相似文献
15.
Lead has been exploited by man over thousands of years for a variety of metallurgical, medicinal, and industrial purposes. The cumulative output of Pb from mining is estimated to be 260 million metric tonnes and 85% of this has occurred over the last two centuries. Global annual production of Pb from mining was about 3 million tonnes at the turn of the millenium. Terrestrial ecosystems all over Norway have been contaminated moderately to strongly by Pb and other trace elements from atmospheric deposition. With the aim of developing a method for mapping the accumulated content of anthropogenic Pb and how deep in the soil profile the atmospherically deposited Pb has penetrated, the concentration of Pb and the 206Pb/207Pb ratio has been studied in podzolic forest soils at four locations with different lithology, i.e. age and type of bedrock, in the Oslo area. The concentrations of Pb in the soil profiles are 6.6–38.1 mg/kg (median 10.3). The 206Pb/207Pb ratio ranges between 1.168 and 1.314 (median 1.267) over the entire profile. In the upper 5 cm the range is 1.168–1.191, similar to ratios determined in recent atmospheric deposition. Applying three different methods, the amount of anthropogenically deposited Pb is estimated at 1–6 t/km2. 相似文献
16.
This study was aimed at evaluating the mechanical and pH-dependent leaching performance of a mixed contaminated soil treated with a mixture of Portland cement (CEMI) and pulverised fuel ash (PFA). It also sought to develop operating envelopes, which define the range(s) of operating variables that result in acceptable performance. A real site soil with low contaminant concentrations, spiked with 3000 mg/kg each of Cd, Cu, Pb, Ni and Zn, and 10,000 mg/kg of diesel, was treated with one part CEMI and four parts PFA (CEMI:PFA = 1:4) using different binder and water contents. The performance was assessed over time using unconfined compressive strength (UCS), hydraulic conductivity, acid neutralisation capacity (ANC) and pH-dependent leachability of contaminants. With binder dosages ranging from 5% to 20% and water contents ranging from 14% to 21% dry weight, the 28-day UCS was up to 500 kPa and hydraulic conductivity was around 10−8 m/s. With leachant pH extremes of 7.2 and 0.85, leachability of the contaminants was in the range: 0.02–3500 mg/kg for Cd, 0.35–1550 mg/kg for Cu, 0.03–92 mg/kg for Pb, 0.01–3300 mg/kg for Ni, 0.02–4010 mg/kg for Zn, and 7–4884 mg/kg for total petroleum hydrocarbons (TPHs), over time. Design charts were produced from the results of the study, which show the water and/or binder proportions that could be used to achieve relevant performance criteria. The charts would be useful for the scale-up and design of stabilisation/solidification (S/S) treatment of similar soil types impacted with the same types of contaminants. 相似文献
17.
When Fe(II) bearing groundwaters surface in streams, particulate authigenic Fe-rich material is produced by oxidation. Such freshly precipitated Fe minerals may be transported as suspended sediment and have a profound impact on the fate of trace metals and nutrients in rivers. The objective of this study was to monitor changes in mineralogy and composition of authigenic material from its source to streams of increasing order. Groundwaters, surface waters, and suspended sediment in streams of different order were sampled in the Kleine Nete catchment (Belgium), a lowland with Fe-rich groundwaters (3.5–53.8 mg Fe/L; pH 6.3–6.9). Fresh authigenic material (>0.45 μm) was produced by oxidising filtered (<0.45 μm) groundwater and surface water. This material contained, on average, 44% Fe, and smaller concentrations of C, P, and Ca. Iron EXAFS (Extended X-ray Absorption Fine Structure) spectroscopy showed that the Fe was present as poorly crystalline hydrous ferric oxides with a structure similar to that of ferrihydrite. The Fe concentration in the suspended sediment samples decreased to 36–40% (stream order 2), and further to 18–26% (stream order 4 and 5). Conversely, the concentrations of organic C, Ca, Si, and trace metals increased with increasing stream order, suggesting mixing of authigenic material with suspended sediment from a different source. The Fe speciation in the suspended sediment was similar to that in fresh authigenic material, but more Fe–Fe interactions were observed, i.e. it was increasingly hydrolysed, suggesting ageing reactions. The suspended sediment in the streams of order 4 and 5 is estimated to contain between 31% and 59% of authigenic material, but more data are needed to refine this estimate. The authigenic material is an important sink for P in these streams which may alleviate the eutrophication risk in this catchment. 相似文献
18.
《Chemie der Erde / Geochemistry》2016,76(3):353-362
Active and abandoned mine activities constitute the sources of deterioration of water and soil quality in many parts of the world, particularly in the African Copperbelt regions. The accumulation in soils and the release of toxic substances into the aquatic ecosystem can lead to water resources pollution and may place aquatic organisms and human health at risk. In this study, the impact of past mining activity (i.e., abandoned mine) on aquatic ecosystems has been studied using ICP-MS analysis for trace metals and Rare Earth Elements (REE) in sediment samples from Lubumbashi River (RL) and Tshamilemba Canal (CT), Katanga, Democratic Republic of the Congo (DRC). Soil samples from surrounding CT were collected to evaluate trace metal and REE concentrations and their spatial distribution. The extent of trace metal contamination compared to the background area was assessed by Enrichment Factor (EF) and Geoaccumulation Index (Igeo). Additionally, the trace metal concentrations probable effect levels (PELs) for their potential environmental impact was achieved by comparing the trace metal concentrations in the sediment/soil samples with the Sediment Quality Guidelines (SQGs). Spearman's Rank-order correlation was used to identify the source and origin of contaminants. The results highlighted high concentrations of trace metals in surface sediments of CT reaching the values of 40152, 15586, 610, 10322, 60704 and 15152 mg kg−1 for Cu, Co, Zn, Pb, Fe and Mn, respectively. In the RL, the concentrations reached the values of 24093, 2046, 5463, 3340, 68290 and 769 mg kg−1 for Cu, Co, Zn, Pb, Fe and Mn, respectively. The ΣREE varied from 66 to 218 and 142–331 mg kg−1 for CT and RL, respectively. The soil samples are characterized by variable levels of trace metals. The EF analysis showed “extremely severe enrichment” for Cu and Co. However, no enrichment was observed for REE. Except for Mo, Th, U, Eu, Mo, Ho and Tm for which Igeo is classified as “moderately polluted and/or unpolluted”, all elements in different sites are classified in the class 6, “extremely polluted”. The trace metal concentrations in all sampling sites largely exceeded the SQGs and the PELs for the Protection of Aquatic Life recommendation. Cu and Co had positive correlation coefficient values (r = 0.741, P < 0.05, n = 14). This research presents useful tools for the evaluation of water contamination in abandoned and active mining areas. 相似文献
19.
Abra is a blind, sedimentary rock-hosted polymetallic Fe–Pb–Zn–Ba–Cu ± Au ± Ag ± Bi ± W deposit, discovered in 1981, located within the easterly trending Jillawarra rift sub-basin of the Mesoproterozoic Edmund Basin, Capricorn Orogen, Western Australia. The Edmund Basin contains a 4–10 km thick succession of siltstone, sandstone, dolomitic siltstone, and stromatolitic dolomite. The age of the Edmund Group is between 1.66 and 1.46 Ga. The Abra polymetallic deposit is hosted in siltstone, dolostone, sandstone and conglomerate of the Irregully and Kiangi Creek Formations, but the mineralised zones do not extend above an erosion surface marking the change from fluvial to marine facies in the lower part of the Kiangi Creek Formation. The Abra deposit is characterised by a funnel-shaped brecciated zone, interpreted as a feeder pipe, overlain by stratiform–stratabound mineralisation. The stratiform–stratabound mineralisation includes a Red Zone and an underlying Black Zone. The Red Zone is characterised by banded jaspilite, hematite, galena, pyrite, quartz, barite, and siderite. The jaspilite and hematite cause the predominant red colouration. The Black Zone consists of veins and rhythmically banded sulphides, laminated and/or brecciated hematite, magnetite, Fe-rich carbonate and scheelite. In both zones, laminations and bands of sulphide minerals, Fe oxides, barite and quartz commonly exhibit colloform textures. The feeder pipe (Stringer Zone) merges with Black Zone and consists of a stockwork of Fe-carbonate-quartz, barite, pyrite, magnetite and chalcopyrite, exhibiting fluidised and/or jigsaw textures.The Abra mineral system is characterised by several overprinting phases of hydrothermal activity, from several stages of brecciation and fluidisation, barite and sulphide veining to barren low-temperature chalcedonic (epithermal regime) veining. Hydrothermal alteration minerals include multi-stage quartz, chlorite, prehnite, Fe-rich carbonate and albite. Albite (Na metasomatism) is an early alteration phase, whereas Fe-rich carbonate is a late phase. Fluid inclusion studies indicate that the ore fluids had temperatures ranging from 162 to 250 °C, with salinities ranging from 5.8 to about 20 wt.% NaCl. In the course of our studies, microthermometric and Raman microprobe analyses were performed on fluid inclusions in carbonate, quartz and barite grains. Fluid inclusions in quartz show homogenisation temperatures ranging from 150 to 170 °C with calculated salinities of between 3.7 and 13.8 wt.% NaCl.The sulphur isotopic system shows δ34S values ranging from 19.4 to 26.6‰ for sulphides and from 37.4 to 41.9‰ for barite (Vogt and Stumpfl, 1987, Austen, 2007). Sulphur isotope thermometry between sulphides and sulphide–barite pairs yields values ranging from 219 to 336 °C (Austen, 2007).Galena samples were analysed for Pb isotope ratios, which have been compared with previous Pb isotopic data. The new Pb isotope systematics show model ages of 1650–1628 Ma, consistent with the formation of the host Edmund Basin.Re–Os dating of euhedral pyrite from the Black Zone yielded an age of ~ 1255 Ma. This age corresponds to the 1320–1170 Ma Mutherbukin tectonic event in the Gascoyne Complex. This event is manifested primarily along a WNW-trending structural corridor of amphibolite facies rocks, about 250 km to the northwest of the Abra area. It is possible that the Re–Os age represents a younger re-activation event of an earlier SEDEX style system with a possible age range of 1640–1590 Ma.A genetic model for Abra is proposed based on the above data. The model involves two end-members ore-forming stages: the first is the formation of the SEDEX style mineral systems, followed by a second multi-phase stage during which there was repeated re-working of the mineral system, guided by seismic activity along major regional faults. 相似文献
20.
Remediation of 56 ML of acidic, contaminant-laden Baal Gammon mine pit water was undertaken using in situ hydrotalcite formation. The pit water composition was modified via the addition of MgCl2·6H2O to form a 2.5:1 M2+:M3+ metal ion ratio followed by the addition of NaOH to increase the pH 10 to induce spontaneous hydrotalcite precipitation. As a result of the in situ hydrotalcite precipitation a broad spectrum of elements of environmental concern including Al, Cd, Co, Cr, Cu, Fe, In, Mn, Mo, Ni, V and Zn were removed from solution. Significantly, an ore grade hydrotalcite precipitate containing Cu (8.0 ± 1.0%) and Zn (3.9 ± 0.5%) was produced directly from the mine pit water column allowing for potential recovery of valuable metals to offset remediation costs. The final water quality produced after in situ remediation was of a simple Na–Cl–SO4 type. 相似文献