Mineralogical,geochemical, and microbial investigation of a sulfide-rich tailings deposit characterized by neutral drainage

Mineralogical, geochemical and microbial characterization of tailings solids from the Greens Creek Mine, Juneau, Alaska, was performed to evaluate mechanisms controlling aqueous geochemistry of near-neutral pH pore water and drainage. Core samples of the tailings were collected from five boreholes ranging from 7 to 26 m in depth. The majority of the 51 samples (77%) were collected from the vadose zone, which can extend >18 m below the tailings surface. Mineralogical investigation indicates that the occurrence of sulfide minerals follows the general order: pyrite [FeS₂] >> sphalerite [(Zn,Fe)S] > galena [PbS], tetrahedrite [(Fe,Zn,Cu,Ag)₁₂Sb₄S₁₃] > arsenopyrite [FeAsS] and chalcopyrite [CuFeS₂]. Pyrite constitutes <20 to >35 wt.% of the tailings mineral assemblage, whereas dolomite [CaMg(CO₃)₂] and calcite [CaCO₃] are present at ?30 and 3 wt.%, respectively. The solid-phase geochemistry generally reflects the mineral assemblage. The presence of additional trace elements, including Cd, Cr, Co, Mo, Ni, Se and Tl, is attributed to substitution into sulfide phases. Results of acid–base accounting (ABA) underestimated both acid-generating potential (AP) and neutralization potential (NP). Recalculation of AP and NP based on solid-phase geochemistry and quantitative mineralogy yielded more representative results. Neutrophilic S-oxidizing bacteria (nSOB) and SO₄-reducing bacteria (SRB) are present with populations up to 10⁷ and 10⁵ cells g⁻¹, respectively. Acidophilic S-oxidizing bacteria (aSOB) and iron-reducing bacteria (IRB) were generally less abundant. Primary influences on aqueous geochemistry are sulfide oxidation and carbonate dissolution at the tailings surface, gypsum precipitation–dissolution reactions, as well as Fe reduction below the zone of sulfide oxidation. Pore-water pH values generally ranged from 6.5 to 7.5 near the tailings surface, and from approximately 7–8 below the oxidation zone. Elevated concentrations of dissolved SO₄, S₂O₃, Fe, Zn, As, Sb and Tl persisted under these conditions.     

Distribution of trace elements in soils surrounding the El Teniente porphyry copper deposit,Chile: the influence of smelter emissions and a tailings deposit

In the area surrounding the El Teniente giant porphyry copper deposit, eight soil sites were sampled at three depth levels in the summer 2004. The sites were selected for their theoretical potential of being influenced by past SO₂ emissions from the smelter and/or seepage from a now idle tailings impoundment. The soil mineralogy, grain size distribution, total organic matter contents, major element composition, cation exchange capacity, and Cu, Mo, Pb, Zn, As and SO₄ ²⁻ concentrations were determined for all samples after nitric acid extraction and separate leaches by ammonium acetate (pH 7) and sodium acetate (pH 5). For water rinses, only Cu could be determined with the analytical set-up used. Cu and SO₄ ²⁻ enrichment in topsoils was found at six sites either downwind from the smelter or within the combined influence of the smelter and the tailings impoundment. Both elements were released partially by ammonium and sodium acetate extractions. Due to the scarce background trace element concentrations of soil and rock outside the immediate mine area, assessment of trace element mobility for Mo, Zn, Pb and As was difficult. Arsenic was found to be concentrated in soil horizons with high smectite and/or organic matter contents. Mo appears to be linked to the presence of windblown tailings sediment in the soils. Mobilization of Mo, Zn, and As for the acetate extractions was minimal or below the detection limits for the AAS technique used. The presence of windblown tailings is considered to be an additional impact on the soils in the foothills of the El Teniente compound, together with the potential of acidity surges and Cu mobilization in topsoils after rainfalls. Two sites located at the western limit of the former SO₂ saturated zone with strongly zeolitized soils and underlying rock did not show any Cu or SO₄ ²⁻ enrichment in the topsoils, and remaining total trace element concentrations were below the known regional background levels.     

Contribution of a Dense Population of the Brittle Star <Emphasis Type="Italic">Acrocnida brachiata</Emphasis> (Montagu) to the Biogeochemical Fluxes of CO<Subscript>2</Subscript> in a Temperate Coastal Ecosystem

The production of organic matter and calcium carbonate by a dense population of the brittle star Acrocnida brachiata (Echinodermata) was calculated using demographic structure, population density, and relations between the size (disk diameter) and the ash-free dry weight (AFDW) or the calcimass. During a 2-year survey in the Bay of Seine (Eastern English Channel, France), organic production varied from 29 to 50 g_AFDW m⁻² year⁻¹ and CaCO₃ production from 69 to 104 g_CaCO3 m⁻² year⁻¹. Respiration was estimated between 1.7 and 2.0 mol_CO2 m⁻² year⁻¹. Using the molar ratio (ψ) of CO₂ released: CaCO₃ precipitated, this biogenic precipitation of calcium carbonate would result in an additional release between 0.5 and 0.7 mol_CO2 m⁻² year⁻¹ that represented 23% and 26% of total CO₂ fluxes (sum of calcification and respiration). The results of the present study suggest that calcification in temperate shallow environments should be considered as a significant source of CO₂ to seawater and thus a potential source of CO₂ to the atmosphere, emphasizing the important role of the biomineralization (estimated here) and dissolution (endoskeletons of dead individuals) in the carbon budget of temperate coastal ecosystems.     

Chemical and isotopic variations in the Wiśniówka Mała mine pit water,Holy Cross Mountains (south-central Poland)

In 2005 and 2006, hydrogeochemical study was carried out in the bipartite Wiśniówka Mała pit lake of the Holy Cross Mountains (south-central Poland). This is the largest acidic water body in Poland. This report presents the element concentrations in the water and sediment, stable sulfur and oxygen isotope ratios in the soluble sulfates, and stable oxygen isotope ratio in the water. The scope of the investigation also encompassed mineralogical examinations (scanning electron microscope, X-ray diffraction) of the sediment. The results of this study show that there is a spatial and temporal variability in concentrations of most elements and sulfur isotope ratios in the examined pit lake. The water of the western pond displayed a lower pH with a mean of 3.73 and higher conductivity (390 μS cm⁻¹) as well as higher concentrations of sulfates (156 mg L⁻¹) and most of the cations and anions. The concentrations of Fe²⁺ and Fe³⁺ averaged 0.8 and 0.4 mg·L⁻¹. In contrast, the eastern pond water revealed a higher pH (mean of 4.36), lower conductivity (293 μS cm⁻¹) and lower sulfate (90 mg L⁻¹) and trace metal levels. Similar variations were recorded in the stable sulfur isotope ratios. The δ³⁴S_V-CDT(SO₄ ²⁻) values in the water of the western pit pond were in the range of −6.7 to −4.6‰ (mean of −5.6‰), whereas that in the eastern pit pond ranged from −2.2 to −0.9‰ (−1.6‰). The alkalinity of the entire lake water was below 0.1 mg·L⁻¹ CaCO₃. No distinct difference in the δ¹⁸O_V-SMOW(SO₄ ²⁻) was noted between the western and eastern pit ponds. Compared to the Purple Pond in the Sudetes (Poland) and similar sites throughout the world, the examined pit lake is highlighted by distinctly low concentrations of sulfates, iron and other trace metals. Based on this and other studies performed in the Holy Cross Mountains, a conclusion can be drawn that the SO₄ ²⁻ in the Wiśniówka Mała pit lake water is a mixture of SO₄ ²⁻ derived from the following sources: (1) pyrite oxidation (especially in the western pond water), (2) leaching of soluble sulfates from soils and waste material, as well as (3) subordinate deposition of airborne sulfate precipitation.     

Thermodynamics of arsenates,selenites, and sulfates in the oxidation zone of sulfide ores: Part III: Eh-pH diagrams of the Me-As-H<Subscript>2</Subscript>O systems (Me = Co,Ni, Fe,Cu, Zn,Pb) at 25°C

The behavior of arsenic at the Earth’s surface and nearby at low temperatures and pressures depends mainly on the redox potential and the acidity-alkalinity of the crystallization media. These parameters determine the migration of arsenic compounds and their precipitation as various solid phases. Understanding the mechanism of arsenic’s behavior under surface conditions, which is important for solving environmental problems, is an urgent task of contemporary mineralogy and geochemistry. The activities of the components in natural waters beyond the zones of natural (oxidation zones) and man-made contamination with arsenic (a _ΣAs = 3 × 10⁻⁸, a _ΣFe = 10⁻⁵, a _ΣCu = 10⁻⁷, a _ΣZn = 5 × 10⁻⁷, a _ΣCo = 10⁻⁸, a _ΣNi = 6 × 10⁻⁸, a _ΣPb = 10⁻⁸) and in waters formed in the oxidation zone (a _ΣSe = 10⁻³, a _ΣFe = 10⁻², a _ΣCu = 10⁻², a _ΣZn = 5 × 10⁻², a _ΣCo = 10⁻³, a _ΣNi = 10⁻², a _ΣPb = 10⁻⁴) have been estimated. Eh-pH diagrams were calculated and plotted using the Geochemist’s Workbench (GMB 7.0) software package. The database comprises the thermodynamic parameters of 46 elements, 47 main particles, 48 redox pairs, 551 particles in solution, 624 solid phases, and 10 gases. The Eh-pH diagrams of the Me-As-H₂O systems (Me = Co, Ni, Fe, Cu, Zn, Pb) were plotted for the average contents of these elements in the underground water and for their higher contents in the oxidation zones of sulfide deposits. The formation of Co, Ni, Fe, Cu, Zn, and Pb arsenates at the surface is discussed.     

Thermodynamics of arsenates,selenites, and sulfates in the oxidation zone of sulfide ores: IV. Eh-pH diagrams of the Me-Se-H<Subscript>2</Subscript>O systems (Me = Co,Ni, Fe,Cu, Zn,Pb) at 25°C

The behavior of selenium at the Earth’s surface and nearby at low temperatures and pressures is controlled by variations of the redox potential and the acidity of solutions. These parameters determine the migration of selenium and its precipitation as various solid phases. Understanding the mechanism of selenium’s behavior under surface conditions, which is important for solving environmental problems, is an urgent task of contemporary mineralogy and geochemistry. The activities of components in natural waters beyond the zones of natural (oxidation zones) and man-made contamination with selenium (a _ΣSe = 10⁻⁹, a _ΣFe = 10⁻⁵, a _ΣCu = 10⁻⁷, a _ΣZn = 5 × 10⁻⁷, a _ΣCo = 10⁻⁸, a _ΣNi = 6 × 10⁻⁸, a _ΣPb = 10⁻⁸) and in waters formed in the oxidation zone (a _ΣSe = 10⁻⁵–10⁻⁴, a _ΣFe = 10⁻², a _ΣCu = 10⁻², a _ΣZn = 5 × 10⁻², a _ΣCo = 10⁻³, a _ΣNi = 10⁻², a _ΣPb = 10⁻⁴) have been estimated. Eh-pH diagrams were calculated and plotted using the Geochemist’s Workbench (GMB 7.0) software package. The database comprises the thermodynamic parameters of 46 elements, 47 main particles, 48 redox pairs, 551 particles in solution, 624 solid phases, and 10 gases. The Eh-pH diagrams of the Me-Se-H₂O systems (Me = Co, Ni, Fe, Cu, Zn, Pb) were plotted for the average contents of these elements in underground water and for their contents in oxidation zones of sulfide deposits. The formation of Co, Ni, Fe, Cu, Zn, and Pb selenites and selenates at the surface is discussed.     

Fluoride ion contamination in the groundwater of Mithi sub-district, the Thar Desert, Pakistan

Groundwater samples were collected from various localities of Mithi sub-district of the Thar Desert of Pakistan and analysed for fluoride ion along with other chemical parameters. The area is mainly covered by sand dunes and kaolin/granite at variable depths. Results showed that collected water samples were severely contaminated by the presence of fluoride ion and most of the samples have higher concentration than prescribed WHO standards (1.5 mg/l) for drinking water. Fluoride ion concentrations ranged between 0.09 and 11.63 mg/l with mean and median values of 3.64 and 3.44 mg/l, respectively, in this area whereas, distribution pattern showed high concentrations in the vicinity of Islamkot and Mithi towns. The content of F⁻ has also been correlated with other major ions found in the groundwater of the study area. The positive correlation of F⁻ with Na⁺ and HCO₃ ⁻ showed that the water with high Na⁺ and HCO₃ ⁻ stabilizes F⁻ ions in the groundwater of the Thar Desert. The pH versus F⁻ plots signifies high fluoride concentration at higher pH values, implying that alkaline environment favours the replacement of exchangeable OH⁻ with F⁻ in the groundwater of Mithi area. The saturation indices (SI) of fluorite (CaF₂) and calcite (CaCO₃) in the groundwater samples showed that most of the samples are oversaturated with respect to calcite whereas majority of samples have been found under saturated with respect to fluorite. The log TDS and Na/Na+Ca ratio reflected supremacy of weathering of rocks, which promotes the availability of fluoride ions in the groundwater. Piper diagram has been used to classify the hydrofacies. In the cation triangle, all samples are Na-type, while the anion triangle reflects major dominance of Cl-type with a minor influence of HCO₃ ⁻ and SO₄ ⁻.     

Early Permian plutons from the northern North China Block: constraints on continental arc evolution and convergent margin magmatism related to the Central Asian Orogenic Belt

Recent zircon dating identified several late Carboniferous to early Permian hornblende gabbro–diorite–quartz diorite–granodiorite–tonalite–granite plutons in lithological assemblages at the northern margin of the North China Block (NCB) that were previously regarded as Archaean to Palaeoproterozoic. Our geochronological results indicate that emplacement of these plutons was a continuous process during the late Carboniferous to early Permian, from 324 ± 6 to 274 ± 6 Ma, and lasted for at least 50 Ma. In this paper, the early Permian components with compositions from gabbro to granite within the intrusive complex were studied. The early Permian plutons exhibit calc-alkaline or high-K calc-alkaline, metaluminous geochemical features and highly variable SiO₂ contents. They have no significant Eu anomaly in their REE patterns, and in primitive-mantle-normalized spidergrams they display depletion in Th, U, Nb, Ta, P and Ti, and enrichment in Ba, K, Pb and Sr. The granitoid bodies within these plutons display I-type and adakitic geochemical signatures. The early Permian rocks exhibit low whole-rock initial ⁸⁷Sr/⁸⁶Sr ratios from 0.70520 to 0.70615 and have negative whole-rock ε _Nd(t) values ranging from −17.4 to −9.3 and zircon ε _Hf(t) values of −23.2 to −10.5. The gabbros exhibit higher ε _Nd(t) values from −11.1 to −9.3 and ε _Hf(t) values from −16.5 to −10.5, and one granodiorite exhibits an even lower ε _Nd(t) value of −17.4 and zircon ε _Hf(t) values of −23.2 to −15.1. Geochemical, Sr–Nd and in situ zircon Hf isotopic compositions suggest that the hornblende gabbros were derived from a metasomatized lithospheric mantle, and the diorite and quartz diorite were generated from a gabbroic magma by fractional crystallization, coupled with differential assimilation of ancient lower crustal material. The granodiorite was likely derived from partial melting of ancient lower crust with involvement of some mantle components. Involvement of both lithospheric mantle and ancient lower crust in the generation of the early Permian plutons indicates strong crust–mantle interaction in the northern NCB. Petrological associations as well as geochemical and Sr–Nd–Hf isotopic results show that the early Permian plutons were emplaced along an Andean-type active continental margin during southward subduction of the Palaeo-Asian oceanic plate beneath the NCB. Integration of our results with previously published data for late Carboniferous and late Permian to middle Triassic intrusions suggests that the continental arc on the northern margin of the NCB existed for at least 50 Ma during the late Palaeozoic, and final amalgamation of the Mongolian arc terranes with the northern NCB likely occurred during a period from ~270 to ~250 Ma, i.e, in the late Permian to earliest Triassic.     

Hydrochemical models of the sulphidic tailings dumps at Matchless (Namibia) and Selebi-Phikwe (Botswana)

The sulphidic tailings dumps at Matchless (Namibia) and Selebi-Phikwe (Botswana) are located in a similar semiarid environment but have a contrasting mineralogical composition. The Matchless tailings are pyrite-rich, whereas the Selebi-Phikwe tailings are dominated by pyrrhotite. Hydrochemical models are established with computer codes for water-balance, sulphide oxidation rate and hydrochemical equilibrium calculations. The data input is based on detailed mineralogical, chemical and kinetic investigations carried out on the core of boreholes drilled in 2000 and 2003. The oxidation of pyrrhotite proceeds at a much faster rate than the oxidation of pyrite. The PYROX code, which is used for kinetic calculations, can take these differences into account by applying different oxide-coating diffusion coefficients (D₂) for pyrrhotite and pyrite. Humidity-cell testing is widely used to predict the post-mining composition of drainage water in humid climates. However, the semiarid conditions at Matchless and Selebi-Phikwe only allow a minimal water flux within the dump. Under such conditions, humidity-cell testing is likely to overestimate the seepage-water pH. This is suggested by the hydrochemical equilibrium calculations for the post-mining period at Selebi-Phikwe, which predict a seepage-water pH about one unit lower than the pH at the end of the 26-weeks humidity-cell testing period. The acidity of the seepage water can be reduced by about half a pH unit, if an oxygen barrier below the evaporation zone is installed. A clay layer 0.5 m thick covered by >1.5 m tailings represents the optimal design for a wet barrier. All three computer codes used for water-balance calculations (HELP3, UNSAT-H and HYDRUS-1D), predict >85% average water saturation for such a layer, which diminishes the diffusion of oxygen into the pile and production of SO₄⁻² and H⁺. The alternative design for a dry barrier consists of a vegetated silt layer 1 m thick on top of the tailings. This barrier does not significantly influence the diffusion of oxygen although it reduces the net infiltration to ≤11 mm/year.     

Geochemistry and Os–Nd–Sr isotopes of the Gaositai Alaskan-type ultramafic complex from the northern North China craton: implications for mantle–crust interaction

We report petrological, chemical and Os–Nd–Sr isotopic data for the Gaositai ultramafic complex from northern North China craton (NCC) to reveal its petrogenesis. The complex shows features of Alaskan-type intrusions, including (1) the concentric zoning from dunite core, to clinopyroxenite and hornblendite in the rim, and the common cumulative textures; (2) the abundance of olivine, clinopyroxene and hornblende, and the scarcity of orthopyroxene and plagioclase, and (3) the systematic decrease in Mg# of ferromagnesian phases from core to rim, accompanied by the Fe-enrichment trend of accessory spinel. The different rock types show highly varied, radiogenic Os isotopic ratios (0.129–5.2), and unradiogenic Nd isotopic composition (ε_Nd(t) = −8 to −15), but are homogeneous in I_Sr ratios (0.7054–0.7066). The (¹⁸⁷Os/¹⁸⁸Os)_i ratios are found to be anti-correlated with ε_Nd(t) values and whole-rock Mg# as well. These data suggest significant crustal contamination during magma evolution. The crustal contaminants are dominantly Archean mafic rocks in the lower crust, and subordinate TTG gneisses at shallower crustal levels. The parental magma was hydrous picritic in composition, derived from an enriched lithospheric mantle source above a subduction zone. The zoned pattern of the complex formed probably through “flow differentiation” of a rapidly rising crystal mush along a fracture zone that was developed as a result of lithospheric extension in a back-arc setting in the northern margin of the NCC at ca. 280 Ma.     

Effect of acid mine drainage on a karst basin: a case study on the high-As coal mining area in Guizhou province,China

Acid mine drainage (AMD) is a common pollution in mining areas due to the oxidation of pyrite and associated sulfide minerals at mines, tailings and mine dumps. Elevated metals (Fe, Mn, Al) and metalloids (As, Hg) in AMD would deteriorate the local aquatic environment and influence the water supply. A carbonate basin with deposits of high-arsenic coal in Xingren County, southwestern China, was chosen to study the behavior of As and other chemical constituents along a river receiving AMD. Heavy metals (Fe, Mn) and major ions such as (Ca²⁺, Mg²⁺, Cl⁻, SO₄ ²⁻) in surface water, and As in sediment and surface water were analyzed. It was found that high concentrations of SO₄ ²⁻ (1,324–7,560 mg/L) and Fe (369–1,472 mg/L) in surface water were mainly controlled by the interactions between water and rocks such as the oxidation of pyrite in the local coal seams, precipitation and adsorption of iron minerals. Although ubiquitous carbonate minerals in the bedrock and the riverbeds, low pH (<3) water was maintained until 2 km downstream from the AMD source due to the Fe(hydro)oxide minerals coating on the surface of carbonate minerals to restrain the neutralization of acidic water. Moreover, the formation of Fe(hydro)oxide precipitations absorbed As was dominated the attenuation of As from water to sediment. Whereas, the dilution also played an important role in decrease of As in river water.     

Fluid evolution at the Variscan front in the vicinity of the Aachen thrust

Quartz–carbonate–chlorite veins were studied in borehole samples of the RWTH-1 well in Aachen. Veins formed in Devonian rocks in the footwall of the Aachen thrust during Variscan deformation and associated fluid flow. Primary fluid inclusions indicate subsolvus unmixing of a homogenous H₂O–CO₂–CH₄–(N₂)–Na–(K)–Cl fluid into a H₂O–Na–(K)–Cl solution and a vapour-rich CO₂–(H₂O, CH₄, N₂) fluid. The aqueous end-member composition resembles that of metamorphic fluids of the Variscan front zone with salinities ranging from 4 to 7% NaCl equiv. and maximum homogenisation temperatures of close to 400°C. Pressure estimates indicate a burial depth between 4,500 and 8,000 m at geothermal gradients between 50 and 75°C/26 MPa, but pressure decrease to sublithostatic conditions is also indicated, probably as a consequence of fracture opening during episodic seismic activity. A second fluid system, mainly preserved in pseudo-secondary and secondary fluid inclusions, is characterised by fluid temperatures between 200 and 250°C and salinities of <5% NaCl equiv. Bulk stable isotope analyses of fluids released from vein quartz, calcite, and dolomite by decrepitation yielded δD_H2O values from −89 to −113 ‰, δ¹³C_CH4 from −26.9 to −28.9‰ (VPDB) and δ¹³C_CO2 from −12.8 to −23.3‰ (VPDB). The low δD and δ¹³C range of the fluids is considered to be due to interaction with cracked hydrocarbons. The second fluid influx caused partial isotope exchange and disequilibrium. It is envisaged that an initial short lived flux of hot metamorphic fluids expelled from the epizonal metamorphic domains of the Stavelot–Venn massif. The metamorphic fluid was focused along major thrust faults of the Variscan front zone such as the Aachen thrust. A second fluid influx was introduced from formation waters in the footwall of the Aachen thrust as a consequence of progressive deformation. Mixing of the cooler and lower salinity formation water with the hot metamorphic fluid during episodic fluid trapping resulted in an evolving range of physicochemical fluid inclusion characteristics.     

Geochemical and Sr-Nd isotopic study of alkaline syenites in Liangtun-Kuangdonggou, Liaoning Province, China： Evidence for enriched mantle before 1.86 Ga and implications

The 1.86 Ga Liangtun-Kuangdonggou complex (LKC) is one of the oldest alkaline syenite bodies so far discovered in China. This syenite suite has elevated contents of total alkali (K2O Na2O), with an average of 10.50%, and a mean Rittmann Index (σ) of 6.48. The intrusions have slightly higher concentrations of K2O than those of Na2O on a weight percent basis, indicating the rocks belong to potassium-rich alkaline syenite series. Total rare-earth element concentrations (∑REE ) of the rocks are relatively high, ranging from 324×10 -6 to 1314×10 -6, with a mean value of 666×10 -6. The REE patterns are subparallel and rightward steep with (La/Yb)N >33, showing mild negative to positive Eu anomalies (δEu: 0.63-1.15). All samples exhibit strong LILE and LREE enrichments and TNT (Nb, Ta, Ti) and P depletions in multi-element spidergrams. On the εSr(t)-εNd(t) correlation diagram, most analytical data points plot within the enriched mantle field with low ( 87Sr/86Sr)i ratios (0.7045-0.7051) and negative εNd(t) values (-3.72--3.97), falling among those kimberlites from Fuxian County, Liaoning Provinve, from Mengyin County, Shandong Province and the Ⅱ-type kimberlites from South Africa. These characteristics imply that the LKC-rocks may have the same source as the above-mentioned kimberlites, i.e., they have close connections to the materials derived from enriched mantle reservoirs, further revealing that the upper mantle beneath the northeastern part of the North China Plate had been highly enriched before 1.86 Ga. Geodynamically, the LKC-rocks were formed in a within-plate environment with close genetic connections to rift-related alkaline magma activities possibly controlled by ancient mantle plumes.     

Early Paleozoic adakite in the Liuyuan area from the Beishan orogenic belt,NW Gansu Province: Petrogenesis and implication for tectonic setting

The Liuyuan area,which is located on the southern margin of the Beishan orogenic belt,develops abundant Early Paleozic granitoids.SHRIMP zircon U-Pb dating yielded a weighted mean 206Pb/238U age of 421±8 Ma for the Liuyuan granodiorite(Zhao Zehui et al.,2007),implying its Late Silurian intrusion.Geochemical compositions showed that the Liuyuan granodiorite is characterized by high SiO2(65.01%-67.31%),A12O3(17.17%-18.05%) and Na2O(Na2O/K2O=1.67-1.87) but low Mg# contents calculated as 100×Mg2+/(Mg2++∑Fe2+) from 28.77 to 31.15,as well as being enriched in Sr(472×10-6-517×10-6) but depleted in Yb(1.2×10-6-1.42×10-6) and Y(12.8×10-6-14×10-6).The REEs are characterized by right-inclined patterns with LREE enrichment,HREE depletion and slightly negative Eu anomalies(Eu/Eu*=0.91-0.97).Major and trace elements indicate that the granodiorite is an adakite.The Nb/Ta values of the granodiorite vary from 10.80 to 18.01 and Nb/U from 6.32 to 10.09,both lying between the values of the crust and the mantle.The rock has low εNd(t) values(-2.5--0.8) and high ISr(0.706321-0.706495).Geochemical and Sr-Nd isotopic compositions indicate that the Liuyuan granodiorite is possibly derived from partial melting of thickening lower crust,related to mantle underplating.The Yb-Ta and Y+Nb-Rb discriminant diagrams imply the Liuyuan granodiorite intruded in a local extensional tectonic setting during late collision.Combined with previous studies on geochronology,geochemistry and tectonic setting of granitoids,we interprete that the constraint of this adakite in the Liuyuan area indicates that the tectonic setting may have transformed from collision to extension during the Early Devonian.     

Distribution and Origin of Underground Water Chemical Fields in Songliao Continental Oil—Bearing Sedimentary Basin

There are many factors affecting ungerground water chemistry of an oil-bearing sedimentary basin.The properties of underground water show variations in the vertical direction, giving rise to a vertical zonation with respect to underground water chemistry,Five zones could be divided downwards,including 1)The freshening zone due to meteoric water leaching (A):2)the evaporation-concentration zone near the surface(B);3) the freshening zone due to stratum compaction-released water(C1)-infiltration-concentration zone during the mudstone compaction and water releasing(C2);4) the freshening zone for clay mineral dehydration(D);and 5)the seepage-concentration zone(E).The hydrodynamic fields in the Songliao Basin are obviously asymmetrical,with the characteristics of gravity-induced centripetal flow recharged by meteoric water along the edge to the inner part of the basin mainly in its northern and eastern regions,centrifugal flow and crossformational flow in the center of the basin,as well as the cross-formation flow-evaporation discharge area in its southern area.Hydrodynamics controls the planar distribution of underground-water chemical fields;1)the freshening area due to penetrating meteoric water generally at the basin edges;2)the freshening area for mudstone compaction-released water at the center of the basin;3) the cross-formational area as the transitional aqrea;and 4)the concentration area by cross-formational flow and evaporation.The mineralization degree and the concentrations of Na^ and Cl^- and their salinity coefficeents tend to increase,while the concentrations of(CO3^2- HCO3^-) and SO4^2- and the metamorphism and desulfuration coefficients tend to decrease along the centrifugal flow direction caused by mudstone compaction in the depression area.But all of them tend to increase along the gravity-induced centripetal flow direction.     

Elemental geochemistry and Nd isotopic characteristics of the metasedimentary rocks from the metamorphic belt in central Jiangxi： Provenance and tectonically environmental constraints

The metamorphic belt in central Jiangxi, located in the compound terrain within the Cathaysia, Yangtze Block and Caledonian fold zone of South China, is composed dominantly of meta-argillo-arenaceous rocks, with minor amphibolite. These rocks underwent amphibolite-facies metamorphism. The meta-argillo-arenaceous rocks show large variations in major element composition, but have similar REE patterns and trace element composition, incompatible element and LIE enrichments [ high Th/Sc (0.57-3.59) , La/Sc ( 1.46 - 12.4), La/Yb (5.84 - 19.0) ] and variable Th/U ratios, with ∑REE = 129-296μg/g, δEu =0.51 -0.86, and (La/Yb)N = 3.95 -12.9. The Nd isotopic model ages tDM of these rocks vary from 1597 to 2124 Ma. Their 143 Nd/144 Nd values are low [εNd (0) = - 11.4 to -- 15.8]. Some conclusions have been drawn as follows: (1) The metamorphic rocks in central Jiangxi Province are likely formed in a tectonic environment at the passive continental margin of the Cathaysia massif. (2) The metamorphosed argillo-arenaceous rocks are composed dominantly of upper crustal-source rocks (Al- and Krich granitic or/and sedimentary rocks of Early Proterozoic), which experienced good sorting, slow deposition and more intense chemical weathering. (3) According to the whole-rock Sm-Nd isochron ages (1113±49 to 1199 ± 26 Ma) of plagioclase-amphibole (schist) and Nd isotopic model age tDM ( 1597 - 2124Ma) of meta-argillo-arenaceous rocks, the metamorphic belt in central Jiangxi Province was formed during the Middle Proterozoic ( 1100 - 1600 Ma).     

Water quality assessment of groundwater in some rock types in parts of the eastern region of Ghana

A baseline study involving analyses of subsurface water samples from the Cape Coast granitoid complex, Lower Birimian, Togo Formation and the Voltaian Group, was carried out to assess their suitability for drinking, domestic and agricultural purposes. Study results show that pH within the range (3.0 ≤ pH ≤ 6.5) constitutes 74% of the boreholes analysed, and 51% have hardness values ranging from 7.89 to 73.24 mg/l as CaCO₃ and are described as soft. Total dissolved solids are less than 1,000 mg/l and generally characterized by low conductivity values, of which 95% are within the range (55 ≤ EC ≤ 1,500 μS/cm). The mean values of the major cations (Ca²⁺, Mg²⁺, Na⁺, K⁺) and anions (SO₄²⁻, Cl⁻, HCO₃⁻) are all within the World Health Organisation (WHO) standards. Five (5) of the boreholes sampled have nitrate (NO₃⁻) contamination. Even though NO₃⁻ contamination and acidic waters exist in some of the boreholes, the majority of the boreholes are excellent for drinking and domestic purposes. Assessment of the groundwaters for agricultural irrigation revealed three main categories. These are low salinity–low sodicity (C1–S1), medium salinity–low sodicity (C2–S1) and high salinity–low sodicity (C3–S1), using the US Salinity Laboratory (USSL) classification scheme. As much as 95% of the samples plotted in the ‘excellent to good’ and ‘good to permissible’ categories on the Wilcox diagram. The groundwater in the study area may therefore be regarded as good for irrigation activities. The major identifiable geochemical processes responsible for the evolution of the various ions are mineral weathering and chemical reactions.     

Fluid inclusion and stable isotope (O, H, C, and S) constraints on the genesis of the Serrinha gold deposit, Gurupi Belt, northern Brazil

The Serrinha gold deposit of the Gurupi Belt, northern Brazil, belongs to the class of orogenic gold deposits. The deposit is hosted in highly strained graphitic schist belonging to a Paleoproterozoic (∼2,160 Ma) metavolcano-sedimentary sequence. The ore-zones are up to 11 m thick, parallel to the regional NW–SE schistosity, and characterized by quartz-carbonate-sulfide veinlets and minor disseminations. Textural and structural data indicate that mineralization was syn- to late-tectonic and postmetamorphic. Fluid inclusion studies identified early CO₂ (CH₄-N₂) and CO₂ (CH₄-N₂)-H₂O-NaCl inclusions that show highly variable phase ratios, CO₂ homogenization, and total homogenization temperatures both to liquid and vapor, interpreted as the product of fluid immiscibility under fluctuating pressure conditions, more or less associated with postentrapment modifications. The ore-bearing fluid typically has 18–33mol% of CO₂, up to 4mol% of N₂, and less than 2mol% of CH₄ and displays moderate to high densities with salinity around 4.5wt% NaCl equiv. Mineralization occurred around 310 to 335°C and 1.3 to 3.0 kbar, based on fluid inclusion homogenization temperatures and oxygen isotope thermometry with estimated oxygen fugacity indicating relatively reduced conditions. Stable isotope data on quartz, carbonate, and fluid inclusions suggest that veins formed from fluids with δ¹⁸O_H2O and δD_H2O (310–335°C) values of +6.2 to +8.4‰ and −19 to −80‰, respectively, which might be metamorphic and/or magmatic and/or mantle-derived. The carbon isotope composition (δ¹³C) varies from −14.2 to −15.7‰ in carbonates; it is −17.6‰ in fluid inclusion CO₂ and −23.6‰ in graphite from the host rock. The δ³⁴S values of pyrite are −2.6 to −7.9‰. The strongly to moderately negative carbon isotope composition of the carbonates and inclusion fluid CO₂ reflects variable contribution of organic carbon to an originally heavier fluid (magmatic, metamorphic, or mantle-derived) at the site of deposition and sulfur isotopes indicate some oxidation of the originally reduced fluid. The deposition of gold is interpreted to have occurred mainly in response to phase separation and fluid-rock interactions such as CO₂ removal and desulfidation reactions that provoked variations in the fluid pH and redox conditions.     

Fluctuations in a magmatic sulphur isotope signature from the Pinnacles Mine,New South Wales,Australia

Sulphur isotopic compositions of 29 sulphide samples from the Broken Hill-type Pinnacles Deposit, NSW, are found to cluster at 0%. (mean −0.8‰). The restricted range of the (δ³⁴S) values between −3.5 and + 3.7‰ with a mean of −0.8‰, is interpreted as reflecting partial oxidation of a dominantly magmatic sulphur source. δ³⁴S data for galena samples fall into two groups: (1) isotopically heavier galenas (range −0.7 to 0.0‰; mean −0.4‰) which come mainly from the footwall Zn lode and (2) isotopically lighter galenas (range −3.5 to −0.8‰; mean −2.2‰) which are from the main Pb lode. Sphalerite, pyrrhotite and chalcopyrite have slightly heavier isotopic compositions (range −1.6 to +3.7‰ mean +0.3‰) but exhibit the same stratigraphic differentiation. These data are interpreted as representing fluctuating conditions at the site of ore deposition, in which upwelling hydrothermal fluids were subject to increasing fO₂ and decreasing temperature with time.     

Respiration and Calcification of <Emphasis Type="Italic">Crassostrea gigas</Emphasis>: Contribution of an Intertidal Invasive Species to Coastal Ecosystem CO<Subscript>2</Subscript> Fluxes

Respiration and calcification rates of the Pacific oyster Crassostrea gigas were measured in a laboratory experiment in the air and underwater, accounting for seasonal variations and individual size, to estimate the effects of this exotic species on annual carbon budgets in the Bay of Brest, France. Respiration and calcification rates changed significantly with season and size. Mean underwater respiration rates, deducted from changes in dissolved inorganic carbon (DIC), were 11.4 μmol DIC g⁻¹ ash-free dry weight (AFDW) h⁻¹ (standard deviation (SD), 4.6) and 32.3 μmol DIC g⁻¹ AFDW h⁻¹ (SD 4.1) for adults (80–110 mm shell length) and juveniles (30–60 mm), respectively. The mean daily contribution of C. gigas underwater respiration (with 14 h per day of immersion on average) to DIC averaged over the Bay of Brest population was 7.0 mmol DIC m⁻² day⁻¹ (SD 8.1). Mean aerial CO₂ respiration rate, estimated using an infrared gas analyzer, was 0.7 μmol CO₂ g⁻¹ AFDW h⁻¹ (SD 0.1) for adults and 1.1 μmol CO₂ g⁻¹ AFDW h⁻¹ (SD 0.2) for juveniles, corresponding to a mean daily contribution of 0.4 mmol CO₂ m⁻² day⁻¹ (SD 0.50) averaged over the Bay of Brest population (with 10 h per day of emersion on average). Mean CaCO₃ uptake rates for adults and juveniles were 4.5 μmol CaCO₃ g⁻¹ AFDW h⁻¹ (SD 1.7) and 46.9 μmol CaCO₃ g⁻¹ AFDW h⁻¹ (SD 29.2), respectively. The mean daily contribution of net calcification in the Bay of Brest C. gigas population to CO₂ fluxes during immersion was estimated to be 2.5 mmol CO₂ m⁻² day⁻¹ (SD 2.9). Total carbon release by this C. gigas population was 39 g C m⁻² year⁻¹ and reached 334 g C m⁻² year⁻¹ for densely colonized areas with relative contributions by underwater respiration, net calcification, and aerial respiration of 71%, 25%, and 4%, respectively. These observations emphasize the substantial influence of this invasive species on the carbon cycle, including biogenic carbonate production, in coastal ecosystems.