Environmental assessment of Dhaka City (Bangladesh) based on trace metal contents in road dusts

Geochemical analysis of street dusts was conducted to evaluate the environment of Dhaka City, Bangladesh. Dust samples were collected from different areas (industrial, commercial, and residential) of Dhaka City, and their major, trace and rare earth elements (REE) were determined. Samples from the commercial area had Pb concentrations double those of the industrial and residential areas. Contents of Zn, Cu, Ni, and Cr in the industrial areas were greater than those in the commercial and residential areas. The REE patterns of all dusts in Dhaka are similar and are comparable to the average upper continental crust. The condition of the Dhaka environment was compared to that in Japan and other baseline sediments using Zn–Fe₂O₃ and Pb–Fe₂O₃ diagrams. Zn–Fe₂O₃ trends for the dusts show steep inclination compared to the baseline sediment and the Japanese urban sediment trends. Dhaka lake data show enrichment of Zn over the dusts, suggestive of Zn pollution from poorly controlled industrial sources. In contrast, on the Pb–Fe₂O₃ diagram, Dhaka dusts have greater Pb contents than lake sediments, probably due to the higher traffic density in the commercial area compared to the residential area including the area around the lake. The results suggest that higher levels of Pb and Zn in street dusts in Dhaka can most likely be attributed to the anthropogenic sources like vehicle emissions to the atmosphere and a rapid development.     

Lithogeochemical halos and geochemical vectors to stratiform sediment hosted Zn–Pb–Ag deposits, 1. Lady Loretta Deposit, Queensland

Stratiform sediment hosted Zn–Pb–Ag deposits, often referred to as SEDEX deposits, represent an economically important class of ore, that have received relatively little attention in terms of defining lithochemical halos and geochemical vectors useful to exploration. This study concentrates on the Lady Loretta deposit which is a typical example of the class of Proterozoic SEDEX deposits in northern Australia. We examined the major and trace element chemistry of carbonate-bearing sediments surrounding the deposit and defined a series of halos which extend for several hundred metres across strike and up to 1.5 km along strike. The stratiform ore lens is surrounded by an inner sideritic halo [Carr, G.R., 1984. Primary geochemical and mineralogical dispersion in the vicinity of the Lady Loretta Zn–Pb–Ag deposit, North Queensland. J. Geochem. Expl. 22, 217–238], followed by an outer ankerite/ferroan dolomite halo which merges with low iron dolomitic sediments representative of the regional background compositions. Carbonate within the inner siderite halo varies in composition from siderite to pistomesite (Fe_0.6Mg_0.4CO₃), whereas carbonate in the outer ankerite halo varies from ferroan dolomite to ankerite (Ca_0.5Mg_0.3Fe_0.2CO₃). Element dispersion around the stratiform ore lens is variable with Pb, Cu, Ba and Sr showing very little dispersion (<50 m across strike), Zn and Fe showing moderate dispersion (<100 m) and Mn and Tl showing broad dispersion (<200 m). Within the siderite halo Cu, Mg and Na show marked depletion compared to the surrounding sediments. The magnitude of element dispersion and change in carbonate chemistry around the Lady Loretta orebody has enabled the development of three geochemical vectors applicable to exploration. Whole rock analyses are used to calculate the three vector quantities as follows: (1) SEDEX metal index = Zn + 100Pb + 100Tl; (2) SEDEX alteration index = (FeO + 10MnO)100/(FeO + 10MnO + MgO); (3) manganese content of dolomite: MnO_d = (MnO × 30.41)/CaO. All three vectors increase to ore both across strike and along strike. The manganese content of dolomite (MnO_d) exhibits the most systematic pattern increasing from background values of about 0.2 wt% to a maximum of around 0.6 wt% at the boundary between the ankerite and siderite halos. Siderite within the inner halo contains considerably more Mn with MnO values of 0.4 to 4.0 wt%. It is suggested here that the basket of indices defined at Lady Loretta (Zn, Tl, metal index, alteration index, MnO_d and MnO_s) is applicable in the exploration for stratiform Zn–Pb–Ag deposits in dolomite-rich sedimentary basins generally. The indices defined can firstly assist in the identification of sedimentary units favourable for SEDEX mineralisation, and secondly provide vectors along these units to ore. The alteration index and MnO_d, however, should only be used for exploration dolomitic sequences; they are not recommended for exploration in clastic sequences devoid of carbonates.     

Stratigraphy and base metal mineralization in the Otavi Mountain Land, Northern Namibia—a review and regional interpretation

Sediment-hosted base metal sulfide deposits in the Otavi Mountain Land occur in most stratigraphic units of the Neoproterozoic Damara Supergroup, including the basal Nosib Group, the middle Otavi Group and the uppermost Mulden Group. Deposits like Tsumeb (Pb–Cu–Zn–Ge), Kombat (Cu–Pb–Zn), Berg Aukas (Zn–Pb–V), Abenab West (Pb–Zn–V) all occur in Otavi Group dolostones, whereas siliciclastic and metavolcanic rocks host Cu–(Ag) or Cu–(Au) mineralization, respectively. The Tsumeb deposit appears to have been concentrated after the peak of the Damara orogeny at around 530 Ma as indicated by radiometric age data.Volcanic hosted Cu–(Au) deposits (Neuwerk and Askevold) in the Askevold Formation may be related to ore forming processes during continental rifting around 746 Ma. The timing of carbonate-hosted Pb–Zn deposits in the Abenab Subgroup at Berg Aukas and Abenab is not well constrained, but the stable (S, O, C) and Pb isotope as well as the ore fluid characteristics are similar to the Tsumeb-type ores. Regional scale ore fluid migration typical of MVT deposits is indicated by the presence of Pb–Zn occurrences over 2500 km² within stratabound breccias of the Elandshoek Formation. Mulden Group siliciclastic rocks host the relatively young stratiform Cu–(Ag) Tschudi resource, which is comparable to Copperbelt-type sulfide ores.     

Geochronological framework and Pb, Sr isotope geochemistry of the Qingchengzi Pb–Zn–Ag–Au orefield, Northeastern China

The Qingchengzi orefield in northeastern China, is a concentration of several Pb–Zn, Ag, and Au ore deposits. A combination of geochronological and Pb, Sr isotopic investigations was conducted. Zircon SHRIMP U–Pb ages of 225.3 ± 1.8 Ma and 184.5 ± 1.6 Ma were obtained for the Xinling and Yaojiagou granites, respectively. By step-dissolution Rb–Sr dating, ages of 221 ± 12 Ma and 138.7 ± 4.1 Ma were obtained for the sphalerite of the Zhenzigou Zn–Pb deposit and pyrargyrite of the Ag ore in the Gaojiabaozi Ag deposit, respectively. Pb isotopic ratios of the Ag ore at Gaojiabaozi (²⁰⁶Pb/²⁰⁴Pb = 18.38 to 18.53) are higher than those of the Pb–Zn ores (²⁰⁶Pb/²⁰⁴Pb = 17.66 to 17.96; Chen et al. [Chen, J.F., Yu, G., Xue, C.J., Qian, H., He, J.F., Xing, Z., Zhang, X., 2005. Pb isotope geochemistry of lead, zinc, gold and silver deposit clustered region, Liaodong rift zone, northeastern China. Science in China Series D 48, 467–476.]). Triassic granites show low Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb = 17.12 to 17.41, ²⁰⁷Pb/²⁰⁴Pb = 15.47 to 15.54, ²⁰⁸Pb/²⁰⁴Pb = 37.51 to 37.89) and metamorphic rocks of the Liaohe Group have high ratios (²⁰⁶Pb/²⁰⁴Pb = 18.20 to 24.28 and 18.32 to 20.06, ²⁰⁷Pb/²⁰⁴Pb = 15.69 to 16.44 and 15.66 to 15.98, ²⁰⁸Pb/²⁰⁴Pb = 37.29 to 38.61 and 38.69 to 40.00 for the marble of the Dashiqiao Formation and schist of the Gaixian Formation, respectively).Magmatic activities at Qingchengzi and in adjacent regions took place in three stages, and each contained several magmatic pulses: ca. 220 to 225 Ma and 211 to 216 Ma in the Triassic; 179 to 185 Ma, 163 to 168 Ma, 155 Ma and 149 Ma in the Jurassic, as well as ca. 140 to 130 Ma in the Early Cretaceous. The Triassic magmatism was part of the Triassic magmatic belt along the northern margin of the North China Craton produced in a post-collisional extensional setting, and granites in it formed by crustal melting induced by mantle magma. The Jurassic and Early Cretaceous magmatism was related to the lithospheric delamination in eastern China. The Triassic is the most important metallogenic stage at Qingchengzi. The Pb–Zn deposits, the Pb–Zn–Ag ore at Gaojiabaozi, and the gold deposits were all formed in this stage. They are temporally and spatially associated with the Triassic magmatic activity. Mineralization is very weak in the Jurassic. Ag ore at Gaojiabaozi was formed in the Early Cretaceous, which is suggested by the young Rb–Sr isochron age, field relations, and significantly different Pb isotopic ratios between the Pb–Zn–Ag and Ag ores. Pb isotopic compositions of the Pb–Zn ores suggest binary mixing for the source of the deposits. The magmatic end-member is the Triassic granites and the other metamorphic rocks of the Liaohe Group. Slightly different proportions of the two end-members, or an involvement of materials from hidden Cretaceous granites with slightly different Pb isotopic ratios, is postulated to interpret the difference of Pb isotopic compositions between the Pb–Zn–(Ag) and Ag ores. Sr isotopic ratios support this conclusion. At the western part of the Qingchengzi orefield, hydrothermal fluid driven by the heat provided by the now exposed Triassic granites deposited ore-forming materials in the low and middle horizons of the marbles of the Dashiqiao Formation near the intrusions to form mesothermal Zn–Pb deposits. In the eastern part, hydrothermal fluids associated with deep, hidden Triassic intrusions moved upward along a regional fault over a long distance and then deposited the ore-forming materials to form epithermal Au and Pb–Zn–Ag ores. Young magmatic activities are all represented by dykes across the entire orefield, suggesting that the corresponding main intrusion bodies are situated in the deep part of the crust. Among these, only intrusions with age of ca. 140 Ma might have released sufficient amounts of fluid to be responsible for the formation of the Ag ore at Gaojiabaozi.Our age results support previous conclusions that sphalerite can provide a reliable Rb–Sr age as long as the fluid inclusion phase is effectively separated from the “sulfide” phase. Our work suggests that the separation can be achieved by a step-resolution technique. Moreover, we suggest that pyrargyrite is a promising mineral for Rb–Sr isochron dating.     

Environmental impact of the former Pb–Zn mining and smelting in East Belgium

In the mining district of Plombières-La Calamine (East Belgium), extensive Pb–Zn mining activities resulted in an important contamination of overbank sediments along the Geul river. Moreover, a huge amount of heavy metals is stored in a dredged mine pond tailing, which is located along the river. In the dredged mine pond tailing sediments, Pb–Zn minerals control the solubility of Zn, Pb and Cd. Although Pb, Zn and Cd display a lower solubility in overbank sediments compared to the mine tailing pond sediments, elevated concentrations of Pb, Zn and Cd are still found in the porewater of the overbank sediments. The considerable ‘actual’ and ‘potential’ mobility of Zn, Pb and Cd indicates that the mine pond tailing sediments and the overbank sediments downstream from the mine pond tailing represent a considerable threat for the environment. Besides the chemical remobilisation of metals from the sediments, the erosion of overbank sediments and the reworking of riverbed sediments act as a secondary source of pollution.     

Distribution patterns of some heavy metals in the surface sediment fractions at northern Safaga Bay, Red Sea, Egypt

The distribution patterns, the index of geo-accumulations (MI_geo), and the enrichment ratios (ER _n ) of the contaminant metals: Fe, Mn, Zn, Cu, Pb, and Ni were studied in gravel, sand, mud, coarse, medium, and fine sediment fractions of the uppermost layer of the bottom sediments collected from 12 stations covering the northern part of Safaga Bay. The distribution levels of these metals were increasing with grain size decreasing toward the central axis of the bay that extends NE–SW and southward to Safaga Harbour indicating that these metals concentrated mainly in the fine, very fine, and particulate fractions of sediments and to many anthropogenic sources. The geo-accumulation factor of Zn was more significant (MI_geo?≈?0.62–4.23) relative to the other metals. The bay was classified as moderately to strongly polluted by Zn while it is unpolluted to moderately polluted with the other metals with accumulation sequence of: Zn>Ni>Cu>Mn≥Pb. Zn and Ni recorded the highest enrichment ratios (average ER_Zn?≈?3.07 to 8.89; average ER_Ni?≈?0.84 to 3.63) in the different sediment fractions relative the other metals. These enrichment ratios classified the bay as minimal enrichment, suggestive of no or minimal pollution, to significant enrichment, suggestive of a significant pollution signals with metals sequence of: Zn>Ni>Cu>Pb>Mn.     

Geological features and origin of the Huize carbonate-hosted Zn–Pb–(Ag) District, Yunnan, South China

The Huize Zn–Pb–(Ag) district, in the Sichuan–Yunnan–Guizhou Zn–Pb–(Ag) metallogenic region, contains significant high-grade, Zn–Pb–(Ag) deposits. The total metal reserve of Zn and Pb exceeds 5 Mt. The district has the following geological characteristics: (1) high ore grade (Zn + Pb ≥ 25 wt.%); (2) enrichment in Ag and a range of other trace elements (Ge, In, Ga, Cd, and Tl), with galena, sphalerite, and pyrite being the major carriers of Ag, Ge, Cd and Tl; (3) ore distribution controlled by both structural and lithological features; (4) simple and limited wall-rock alteration; (5) mineral zonation within the orebodies; and (6) the presence of evaporite layers in the ore-hosting wall rocks of the Early Carboniferous Baizuo Formation and the underlying basement.Fluid-inclusion and isotope geochemical data indicate that the ore fluid has homogenisation temperatures of 165–220 °C, and salinities of 6.6–12 wt.% NaCl equiv., and that the ore-forming fluids and metals were predominantly derived from the Kunyang Group basement rocks and the evaporite-bearing rocks of the cover strata. Ores were deposited along favourable, specific ore-controlling structures. The new laboratory and field studies indicate that the Huize Zn–Pb–(Ag) district is not a carbonate-replacement deposit containing massive sulphides, but rather the deposits can be designated as deformed, carbonate-hosted, MVT-type deposits. Detailed study of the deposits has provided new clues to the localisation of concealed orebodies in the Huize Zn–Pb–(Ag) district and of the potential for similar carbonate-hosted sulphide deposits elsewhere in NE Yunnan Province, as well as the Sichuan–Yunnan–Guizhou Zn–Pb–(Ag) metallogenic region.     

Supercontinent evolution and the Proterozoic metallogeny of South America

The cratonic blocks of South America have been accreted from 2.2 to 1.9 Ga, and all of these blocks have been previously involved in the assembly and breakup of the Paleoproterozoic Atlantica, the Mesoproterozoic to Neoproterozoic Rodinia, and the Neoproterozoic to Phanerozoic West Gondwana continents. Several mineralization phases have sequentially taken place during Atlantica evolution, involving Au, U, Cr, W, and Sn. During Rodinia assembly and breakup and Gondwana formation, the crust-dominated metallogenic processes have been overriding, responsible for several mineral deposits, including Au, Pd, Sn, Ni, Cu, Zn, Mn, Fe, Pb, U, P₂O₅, Ta, W, Li, Be and precious stones. During Rodinia breakup, epicontinental carbonate-siliciclastic basins were deposited, which host important non-ferrous base metal deposits of Cu–Co and Pb–Zn–Ag in Africa and South America. Isotope Pb–Pb analyses of sulfides from the non-ferrous deposits unambiguously indicate an upper crustal source for the metals. A genetic model for these deposits involves extensional faults driving the circulation of hydrothermal mineralizing fluids from the Archean/Paleoproterozoic basement to the Neoproterozoic sedimentary cover. These relations demonstrate the individuality of metal associations of every sediment-hosted Neoproterozoic base-metal deposit of West Gondwana has been highly influenced by the mineralogical and chemical composition of the underlying igneous and metaigneous rocks.     

Geochemical stream sediment survey in Winder Valley, Balochistan, Pakistan

A pilot scale geochemical survey of sediments from the Winder Stream (SW Pakistan) and its tributaries was carried out. The Winder Stream mainly receives sediment from the southern extensions of the Mor and Pab Ranges in the District of Lasbela (Balochistan). In these two mountain ranges, rocks from Jurassic to Cretaceous age are exposed. Rocks of the Ferozabad Group comprise of carbonates and siliciclastics of Lower–Middle Jurassic age and occupy the dominant part of the Mor Range. These strata host syngenetic and epigenetic Zn–Pb–Ba mineralizations of Stratiform Sediment-Hosted (SSH) and Mississippi Valley Type (MVT) deposits.Quantitative estimates of mobile and immobile elements were made from active stream sediments of the Winder stream and its tributaries. The samples were analyzed for Ag, Zn, Pb, Cu, Ni, Co, V, Mn, Fe and Ba using atomic absorption spectroscopy. The abundance of these elements is discussed in relation to local geological conditions such as bedrock, climate, weathering, mobility and pH of the dispersing waters. A number of Zn anomalies have been distinguished in the study area. Kharrari (Zn, 360 ppm), Sand (Zn, 340 ppm) and Draber (Zn, 210 ppm) are demarcated as new areas for Zn mineralization. The present study also indicates prospects of Ag, Cu and V in the rocks of the Mor Range.Relationships between various elements have been identified from scattergrams and reflect genetic associations. Whereby the positive correlation between Cu–Zn (0.55, n=18) and Cu–Pb (0.63) is related to possible sulphide mineralization.     

Contamination and potential mobility assessment of heavy metals in urban soils of Hangzhou,China: relationship with different land uses

Concentration and distribution of heavy metals (Cd, Cu, Pb and Zn) in urban soils of Hangzhou, China, were measured based on different land uses. The contamination degree of heavy metals was assessed on the basis of pollution index (PI), integrated pollution index (IPI) and geoaccumulation index (I _geo). The 0.1 mol l⁻¹ HCl extraction procedure and gastric juice simulation test (GJST) were used to evaluate the potential mobility and environmental risk of heavy metals in urban soils. The average concentration of Cd, Cu, Pb and Zn in urban soils was measured at 1.2 (with a range of 0.7–4.6), 52.0 (7.4–177.3), 88.2 (15.0–492.1) and 206.9 (19.3–1,249.2) mg kg⁻¹, respectively. The degree of contamination increased in the order of industrial area (IA) > roadside (RS) > residential and commercial areas (RC) > public park and green areas (PG). The PIs for heavy metals indicated that there is a considerable Cd, Cu, Pb and Zn pollution, which originate from traffic and industrial activities. The IPI of these four metals ranged from 1.6 to 11.8 with a mean of 3.5, with the highest IPI in the industrial area. The assessment results of I _geo also supported that urban soil were moderately contaminated with Cd and to a lesser extent also with Cu, Pb and Zn. The IP and I _geo values reveal the pollution degree of heavy metal was the order of Cd > Pb > Zn ≈ Cu. It was shown that mobility and bioavailability of the heavy metals in urban soils increased in the order of Cd > Cu > Zn ≈ Pb. Owing to high mobility of Cd and Cu in the urban soils, further investigations are needed to understand their effect on the urban environment and human health. It is concluded that industrial activities and emissions from vehicles may be the major source of heavy metals in urban contamination. Results of this study present a rough guide about the distribution and potential environmental and health risk of heavy metals in the urban soils.     

The geochemistry, mineralogy and maturity of gossans derived from volcanogenic Zn–Pb–Cu deposits of the eastern Lachlan Fold Belt, NSW, Australia

The Eastern Highlands of Australia have probably been in existence since the Late Cretaceous or earlier and so there has been ample time for mature gossan profiles to form over outcropping volcanogenic Zn–Pb–Cu mineralisation in the eastern Lachlan Fold Belt. The mature gossan profiles are characterised by the upward progression from supergene sulfides to secondary sulfates, carbonates and phosphates into a Fe-oxide dominated surficial capping which may contain boxwork textures after the original sulfides (as at the Woodlawn massive sulfide deposit). However, the region has locally been subjected to severe erosion and the weathering profile over many deposits is incomplete (immature) with carbonate and phosphate minerals, especially malachite, being found in surficial material. These immature gossans contain more Cu, Pb and Zn but lower As, Sn (and probably Au) than the mature gossans. Although Pb is probably the best single pathfinder for Zn–Pb–Cu VHMS deposits of the eastern Lachlan Fold Belt, Ag, As, Au, Bi, Mo, Sb and Sn are also useful, with most of these elements able to be concentrated in substantial amounts in Fe oxides and alunite–jarosite minerals.     

Sulfur isotopic compositions of the Huize super-large Pb–Zn deposit, Yunnan Province, China: Implications for the source of sulfur in the ore-forming fluids

The Huize Pb–Zn deposit of Yunnan Province, China, is located in the center of the Sichuan–Yunnan–Guizhou Pb–Zn–Ag district. Four primary orebodies (orebody No. 1, No. 6, No. 8 and No. 10), with Pb + Zn reserves from 0.5 Mt to 1 Mt, have been found at depth in this deposit. This paper provides new data on the sulfur isotopic compositions of the four orebodies. The data show that the principal sulfide minerals (galena, sphalerite and pyrite) in the four orebodies are enriched in heavy sulfur, the δ³⁴S values between 10.9‰ and 17.7‰ and where δ³⁴S_pyrite > δ³⁴S_sphalerite > δ³⁴S_galena. The δ³⁴S values of sulfide are close to that of the sulfates from the carbonate strata within the region. The similarity in sulfur isotope composition between sulfides and sulfates indicates the sulfur in the ore-forming fluids was likely derived by thermochemical sulfate reduction of sulfates contained within carbonate units.     

Mineralogy and geochemistry of boehmite-rich coals: New insights from the Haerwusu Surface Mine, Jungar Coalfield, Inner Mongolia, China

Boehmite-rich coal of Pennsylvanian age was discovered earlier at the Heidaigou Surface Mine, Jungar Coalfield, Inner Mongolia, China. This paper reports new results on 29 bench samples of the no. 6 coal from a drill core from the adjacent Haerwusu Surface Mine, and provides new insights into the origin of the minerals and elements present. The results show that the proportion of inertinite in the no. 6 coal is higher than in other Late Paleozoic coals in northern China. Based on mineral proportions (boehmite to kaolinite ratio) and major element concentrations in the coal benches of the drill core, the no. 6 coal may be divided into five sections (I to V). Major minerals in Sections I and V are kaolinite. Sections II and IV are mainly kaolinite with a trace of boehmite, and Section III is high in boehmite. The boehmite is derived from bauxite in the weathered surface (Benxi Formation) in the sediment-source region. The no. 6 coal is rich in Al₂O₃ (8.89%), TiO₂ (0.47%), Li (116 μg/g), F (286 μg/g), Ga (18 μg/g), Se (6.1 μg/g), Sr (350 μg/g), Zr (268 μg/g), REEs (172 μg/g), Pb (30 μg/g), and Th (17 μg/g). The elements are classified into five associations by cluster analysis, i.e. Groups A, B, C, D, and E. Group A (ash–SiO₂–Al₂O₃–Na₂O–Li) and Group B (REE–Sc–In–Y–K₂O–Rb–Zr–Hf–Cs–U–P₂O₅–Sr–Ba–Ge) are strongly correlated with ash yield and mainly have an inorganic affinity. The elements that are negatively or less strongly correlated with ash yield (with exceptions of Fe₂O₃, Be, V, and Ni) are grouped in the remaining three associations: Group C, Se–Pb–Hg–Th–TiO₂–Bi–Nb–Ta–Cd–Sn; Group D, Co–Mo–Tl–Be–Ni–Sb–MgO–Re–Ga–W–Zn–V–Cr–F–Cu; and Group E, S–As–CaO–MnO–Fe₂O₃. Aluminum is mainly distributed in boehmite, followed by kaolinite. The high correlation coefficients of the Li–ash, Li–Al₂O₃, and Li–SiO₂ pairs indicate that Li is related to the aluminosilicates in the coal. The boehmite-rich coal is high in gallium and F, which occur in boehmite and the organic matter. Selenium and Pb are mainly in epigenetic clausthalite fillings in fractures. The abundant rare earth elements in the coal benches were supplied from two sources: the bauxite on the weathered surface of the Benxi Formation and from adjacent partings by groundwater leaching during diagenesis. The light rare earth elements (LREEs) are more easily leached from the partings and incorporated into the organic matter than the heavy REEs, leading to a higher ratio of LREEs to HREEs in the coal benches than in the overlying partings.     

Assessment of heavy metals contamination in urban topsoil from Changchun City,China

Due to the rapid urbanization and industrialization that has occurred in China over the last few decades, metals have been continuously emitted into the urban environment and now pose a serious threat to human health. Indeed, there is a growing concern over the potential for pollution of urban soils with heavy metals. Therefore, an extensive soil survey was conducted in urban areas of Changchun, China, to evaluate the current status of heavy metal contamination in soils and to evaluate its potential sources. A total of 352 samples of urban soils were collected from urban areas of Changchun using a systematic sampling strategy in which one sample per km² was taken (0 ~ 20 cm). The levels of Cu, Pb, Zn and the major elements (Mn, Al₂O₃, CaO, Fe₂O₃, MgO, SiO₂, K₂O and NaO) were then determined by X-Ray fluorescence spectrometry (XRF), while the level of Cd was determined by graphite furnace atomic absorption spectrometry (GF-AAS), and the Hg and As concentrations were determined by atomic fluorescence spectroscopy (AFS). The results indicated that, when compared with the background values of topsoil in the Changchun region, the topsoil in urban areas were enriched with metals, particularly Cu, Cd, Zn, Pb and Hg. The results of correlation coefficient analysis showed that Hg, As, Cd, Cu, Pb and Zn were significantly positive correlated with each other, while Cr and Mn formed another group. Moreover, significantly positive correlations were observed between pH and Zn, Pb, Cu, Cd, As and Hg, indicating that pH influences the distributions of these metals in urban soils in Changchun. Principal component analysis (PCA) was conducted to identify sources of heavy metals and the results revealed distinctly different associations among the trace metals and the major elements in the urban soils. The concentration of Cr appeared to be controlled by the parent material (natural sources), while Cu, Pb and Zn were mainly from vehicle emissions, with Zn primarily coming from vehicle tires. Additionally, Hg and As primarily originated from coal combustion, while Cd was mainly associated with industrial sources. According to the pollution index (PI) of each metal, the overall levels of metal pollution were not especially high, but there were clearly contaminated sites concentrated in the central and northeast portion of the studied region. The Nemerow integrated pollution index (NIPI) of the seven metals also indicated that urban soils in Changchun city were classified as having low level of pollution.     

Modeling of fluid pressure evolution related to sediment loading and thrust faulting in the Lanping basin: Implications for the formation of the Jinding Zn–Pb deposit, Yunnan, China

The Jinding Zn–Pb deposit occurs in Cretaceous and Paleocene siliciclastic rocks (mainly sandstones) in the Meso-Cenozoic Lanping basin, western Yunnan, China. With a reserve of approximately 200 Mt of ore containing 6.1% Zn and 1.3% Pb, Jinding is the largest sandstone-hosted Zn–Pb deposit in the world. Most previous studies assumed that the mineralizing fluids were derived from within the basin (including meteoric recharge), and the fluid flow was driven by topographic relief under a hydrostatic regime. In contrast, we propose that the mineralizing system was strongly overpressured based on observations of hydraulic fractures and fluid inclusion data. Numerical modeling results indicate that the overpressures could not have been produced by normal sediment compaction. Thrust faulting and input of mantle-derived fluids are likely responsible for the building-up of the high overpressures. The special hydrodynamic regime and potential contribution of mantle-derived fluids to the mineralizing system distinguish Jinding from other known sedimentary basin-related Pb–Zn deposits.     

Draa Sfar, Morocco: A Visean (331 Ma) pyrrhotite-rich, polymetallic volcanogenic massive sulphide deposit in a Hercynian sediment-dominant terrane

Draa Sfar is a Visean, stratabound, volcanogenic massive sulphide ore deposit hosted by a Hercynian carbonaceous, black shale-rich succession of the Jebilet terrane, Morocco. The ore deposit contains 10 Mt grading 5.3 wt.% Zn, 2 wt.% Pb, and 0.3 wt.% Cu within two main massive sulphides orebodies, Tazakourt (Zn-rich) and Sidi M'Barek (Zn–Cu rich). Pyrrhotite is by far the dominant sulphide (70 to 95% of total sulphides), sphalerite is fairly abundant, chalcopyrite and galena are accessory, pyrite, arsenopyrite and bismuth minerals are rare. Pyrrhotite is monoclinic and mineralogical criteria indicate that it is of primary origin and not formed during metamorphism. Its composition is very homogeneous, close to Fe₇S₈, and its absolute magnetic susceptibility is 2.10^− 3 SI/g. Ar–Ar dating of hydrothermal sericites from a coherent rhyolite flow or dome within the immediate deposit footwall indicates an age of 331.7 ± 7.9 Ma for the Draa Sfar deposit and rhyolite volcanism.The Draa Sfar deposit has undergone a low-grade regional metamorphic event that caused pervasive recrystallization, followed by a ductile–brittle deformation event that has locally imparted a mylonitic texture to the sulphides and, in part, is responsible for the elongated and sheet-like morphology of the sulphide orebodies. Lead isotope data fall into two compositional end-members. The least radiogenic end-member, (²⁰⁶Pb/²⁰⁴Pb = 18.28), is characteristic of the Tazakourt orebody, whereas the more radiogenic end-member (²⁰⁶Pb/²⁰⁴Pb  18.80) is associated with the Sidi M'Barek orebody, giving a mixing trend between the two end-members. Lead isotope compositions at Draa Sfar testify to a significant continental crust source for the base metals, but are different than those of the Hajar and South Iberian Pyrite Belt VMS deposits.The abundance of pyrrhotite versus pyrite in the orebodies is attributed to low fO₂ conditions and neither a high temperature nor a low aH₂S (below 10^− 3) is required. The highly anoxic conditions required to stabilize pyrrhotite over pyrite are consistent with formation of the deposit within a restricted, sediment-starved, anoxic basin characterized by the deposition of carbonaceous, pelagic sediments along the flank of a rhyolitic flow-dome complex that was buried by pelitic sediments. Deposition of sulphides likely occurred at and below the seafloor within anoxic and carbonaceous muds.Draa Sfar and other Moroccan volcanogenic massive sulphide deposits occur in an epicontinental volcanic domain within the outer zone of the Hercynian belt and formed within a sedimentary environment that has a high pelagic component. In spite of the diachronous emplacement between the IPB deposits (late Devonian to Visean) and Moroccan deposits (Dinantian), all were formed around 340 ± 10 Ma following a major phase of the Devonian compression.     

Petrochemical evidence on the probable origin of ferriferous metasediments in western Bushmanland

The mineralized Proterozoic metasediments of Bushmanland are characterized by the presence of ferriferous rocks. This includes banded and unbanded iron formations and various types of gossans. These units are not laterally extensive and occur in different stratigraphic levels. The prevalent minerals in the ferriferous rocks are hematite, magnetite, quartz, garnet, muscovite, biotite and sillimanite, but less common occurrences of graphite, alunite, plumbojarosite, gahnite and dufrenite have been noted. The chemical variation (wt%) is extensive: total Fe₂O₃ (1.3–93.5), SiO₂ (4–93), Al₂O₃ (0.2–14.0), CaO (0.02–20.7), MnO (0.0–14.3), MgO (0.0–5.7), TiO₂ (0.0–4.4), Na₂O (0.0–2.0), K₂O (0.0–1.5) and P₂O₅ (0.1–7.0). The preliminary nature of the data set precludes, however, firm conclusions regarding stratigraphic control of the chemical composition. The trace-element contents (ppm) extend over several orders of magnitude: Zn (0–7,000), Ba (0–5,200), Cu (0–1,400), Pb (0–1,070) and Ni (6–540). Collectively, the data indicate that most of the ferriferous rocks represent highly metamorphosed sediments.     

Environmental conditions inferred from multi-element concentrations in sediments off Cauvery delta,Southeast India

We present multi-element concentrations in the surface sediments from the offshore of Cauvery delta of southeast India to evaluate the impact of coastal pollution on the geochemical behaviour of surface deposits. For this study, 16 surface sediment samples were collected from the offshore of Cauvery delta of southeast India and were analysed using traditional XRF for various major (SiO₂, Al₂O₃, MgO, Fe₂O₃, MnO, Na₂O, K₂O, CaO, P₂O₅, TiO₂) and trace elements (Rb, Sr, Ba, Y, Zr, Nb, V, Cr, Co, Ni, Cu, Zn, Th, Pb) after powdering it to ASTM 230 (<63 μm). The main objectives of this study were to understand the geochemical behaviour of the coastal surface sediments and its performance and relation with the pollution indices and statistical analysis. To meet out the objective, pollution indices such as enrichment factor (EF), contamination factor (CF) and Geoaccumulation Index (I _geo) were calculated and statistical analyses were performed to understand the relationship between the geochemical parameters. Both EF and I _geo show the enrichment of Cu, Cr and Zr, whereas CF shows enrichment of Cu and Cr. Statistical analyses exhibit poor correlation between these elements and fine fraction indicating the insignificant role played by both grain size and organic matter. Strong positive association between Cu and Zn with CaCO₃ exhibits the role of carbonates in precipitating these metals from the overlying water column possibly related to agricultural pollution. Distribution and association of other elements suggest the influence of mineralogy in geochemical composition of surface sediments. Based on this study, we suggest that environmental indices alone should not be considered for evaluating environmental conditions and a prior geogenic characterisation of the sediments is necessary.     

Computer thermodynamic modeling of the transport and deposition of Sb and Au during the formation of Au-Sb deposits

Using the Chiller computer program, we performed modeling of the mechanisms of the joint transport and deposition of Au and Sb from various ore-forming solutions during the formation of Au-Sb deposits. Three models are considered by the example of the Uderei Au-Sb deposit in the Yenisei Ridge: (1) simple cooling (cooling only), (2) iso-enthalpy boiling (P = f(T)), and (3) solution–rock interaction (rock titration model). The behavior of Sb(III) and Au(I) in the system Au–Sb–Fe–Cu–Pb–Zn–As–H₂O–Cl–H₂S–CO₂ under hydrothermal conditions was studied. It is shown that both weakly alkaline (near-neutral) and reduced acidic Fe_aq²⁺-enriched low-chloride high-CO₂ and high-chloride hydrothermal solutions play a crucial role in the formation of gold parageneses of Au-Sb ores.     

2: Hydrothermal ore deposits related to post-orogenic extensional magmatism and core complex formation: The Rhodope Massif of Bulgaria and Greece

The Rhodope Massif in southern Bulgaria and northern Greece hosts a range of Pb–Zn–Ag, Cu–Mo and Au–Ag deposits in high-grade metamorphic, continental sedimentary and igneous rocks. Following a protracted thrusting history as part of the Alpine–Himalayan collision, major late orogenic extension led to the formation of metamorphic core complexes, block faulting, sedimentary basin formation, acid to basic magmatism and hydrothermal activity within a relatively short period of time during the Early Tertiary. Large vein and carbonate replacement Pb–Zn deposits hosted by high-grade metamorphic rocks in the Central Rhodopean Dome (e.g., the Madan ore field) are spatially associated with low-angle detachment faults as well as local silicic dyke swarms and/or ignimbrites. Ore formation is essentially synchronous with post-extensional dome uplift and magmatism, which has a dominant crustal magma component according to Pb and Sr isotope data. Intermediate- and high-sulphidation Pb–Zn–Ag–Au deposits and minor porphyry Cu–Mo mineralization in the Eastern Rhodopes are predominantly hosted by veins in shoshonitic to high-K calc-alkaline volcanic rocks of closely similar age. Base-metal-poor, high-grade gold deposits of low sulphidation character occurring in continental sedimentary rocks of synextensional basins (e.g., Ada Tepe) show a close spatial and temporal relation to detachment faulting prior and during metamorphic core complex formation. Their formation predates local magmatism but may involve fluids from deep mantle magmas.The change in geochemical signatures of Palaeogene magmatic rocks, from predominantly silicic types in the Central Rhodopes to strongly fractionated shoshonitic (Bulgaria) to calc-alkaline and high-K calc-alkaline (Greece) magmas in the Eastern Rhodopes, coincides with the enrichment in Cu and Au relative to Pb and Zn of the associated ore deposits. This trend also correlates with a decrease in the radiogenic Pb and Sr isotope components of the magmatic rocks from west to east, reflecting a reduced crustal contamination of mantle magmas, which in turn correlates with a decreasing crustal thickness that can be observed today. Hydrogen and oxygen isotopic compositions of the related hydrothermal systems show a concomitant increase of magmatic relative to meteoric fluids, from the Pb–Zn–Ag deposits of the Central Rhodopes to the magmatic rock-hosted polymetallic gold deposits of the Eastern Rhodopes.