Tantalo–Niobate from the Apollo-17 Regolith

Doklady Earth Sciences - Particles of tantalo–niobate of the ferrotantalite-manganotantalite series are discovered for the first time in two lunar regolith fragments delivered by the...     

Oil geochemistry derived from the Qinjiatun–Qikeshu oilfields: insight from light hydrocarbons

A suite of 27 oils from the Qinjiatun–Qikeshu oilfields in the Lishu Fault Depression of the Songliao Basin was analyzed using whole oil gas chromatography. In combination with the relative distribution of C₂₇, C₂₈, and C₂₉ regular steranes, detailed geochemical analyses of light hydrocarbons in oil samples revealed crude oils characterized by the dual input of lower aquatic organisms and higher terrestrial plants. Several light hydrocarbon indicators suggest that the liquid hydrocarbons have maturities equivalent to vitrinite reflectances of around 0.78%–0.93%. This is consistent with the maturity determination of steranes C₂₉ 20S/(20S + 20R) and C₂₉ ααβ/(ααα + αββ). Crude oils derived from the two distinct oilfields likely both have source rocks deposited in a lacustrine environment based on light hydrocarbon parameters and on higher molecular weight hydrocarbon parameters. The results show that light hydrocarbon data in crude oils can provide important information for understanding the geochemical characteristics of the Qinjiatun–Qikeshu oils during geologic evolution.     

Evans blue removal from wastewater by rarasaponin–bentonite

The feasibility of natural bentonite and rarasaponin–bentonite for Evans blue removal from aqueous solution was studied. Rarasaponin is a natural surfactant obtained from Sapindus rarak DC was used as modifying agent for natural bentonite modification. Adsorption experiments were conducted in a batch system at various temperatures. Several temperature-dependent isotherm models (Langmuir, Freundlich, Sips and Toth) were used to represent equilibrium data. It was found that Toth model represents the adsorption equilibrium data better than other models. Kinetic data were best represented by the pseudo-first order model. The controlling mechanism of the adsorption of Evans blue onto natural bentonite and rarasaponin–bentonite was physical adsorption.     

Multistage growth of Fe–Mg–carpholite and Fe–Mg–chloritoid,from field evidence to thermodynamic modelling

We provide new insights into the prograde evolution of HP/LT metasedimentary rocks on the basis of detailed petrologic examination, element-partitioning analysis, and thermodynamic modelling of well-preserved Fe–Mg–carpholite- and Fe–Mg–chloritoid-bearing rocks from the Afyon Zone (Anatolia). We document continuous and discontinuous compositional (ferromagnesian substitution) zoning of carpholite (overall X _Mg = 0.27–0.73) and chloritoid (overall X _Mg = 0.07–0.30), as well as clear equilibrium and disequilibrium (i.e., reaction-related) textures involving carpholite and chloritoid, which consistently account for the consistent enrichment in Mg of both minerals through time, and the progressive replacement of carpholite by chloritoid. Mg/Fe distribution coefficients calculated between carpholite and chloritoid vary widely within samples (2.2–20.0). Among this range, only values of 7–11 correlate with equilibrium textures, in agreement with data from the literature. Equilibrium phase diagrams for metapelitic compositions are calculated using a newly modified thermodynamic dataset, including most recent data for carpholite, chloritoid, chlorite, and white mica, as well as further refinements for Fe–carpholite, and both chloritoid end-members, as required to reproduce accurately petrologic observations (phase relations, experimental constraints, Mg/Fe partitioning). Modelling reveals that Mg/Fe partitioning between carpholite and chloritoid is greatly sensitive to temperature and calls for a future evaluation of possible use as a thermometer. In addition, calculations show significant effective bulk composition changes during prograde metamorphism due to the fractionation of chloritoid formed at the expense of carpholite. We retrieve P–T conditions for several carpholite and chloritoid growth stages (1) during prograde stages using unfractionated, bulk-rock XRF analyses, and (2) at peak conditions using compositions fractionated for chloritoid. The P–T paths reconstructed for the Kütahya and Afyon areas shed light on contrasting temperature conditions for these areas during prograde and peak stages.     

Mid–Late Triassic metamorphic event for Changhai meta-sedimentary rocks from the SE Jiao–Liao–Ji Belt,North China Craton: Evidence from monazite U–Th–Pb and muscovite Ar–Ar dating

The precise constraints on the timing of metamorphism of the Changhai metamorphic complex is of great importance considering the prolonged controversial issue of the north margin and the extension of the Sulu–Dabie HP–UHP Belt. While the monazite U–Th–Pb and muscovite ⁴⁰Ar/³⁹Ar techniques are widely accepted as two of the most powerful dating tools for revealing the thermal histories of medium–low grade metamorphic rocks and precisely constraining the timing of metamorphism. The Changhai metamorphic complex at the SE Jiao–Liao–Ji Belt, North China Craton consists of a variety of pelitic schist and Grt–Ky-bearing paragneiss, and minor quartzite and marble. Analyses of mineral inclusions and back-scattered electric (BSE) images of monazites, combined with LA–ICP–MS U–Th–Pb ages for monazites and ⁴⁰Ar/³⁹Ar ages for muscovites, provide evidence of the origin and metamorphic age of the Changhai metamorphic complex. Monazites separates from various Grt–Mus schists and Grt–Ky–St–Mus paragneisses exhibit homogeneous BSE images from cores to rims, and contain inclusion assemblages of Grt + Mus + Qtz ± Ctd ± Ky in schist, and Grt + Ky + St + Mus + Pl + Kfs + Qtz inclusions in paragneiss. These inclusion assemblages are very similar to matrix minerals of host rocks, indicating they are metamorphic rather than inherited or detrital in origin. LA–ICP–MS U–Th–Pb dating reveals that monazites of schist and paragneiss have consistent ²⁰⁶Pb/²³⁸U ages ranging from 228.1 ± 3.8 to 218.2 ± 3.7 Ma. In contrast, muscovites from various schists show slightly older ⁴⁰Ar/³⁹Ar plateau ages of 236.1 ± 1.5 to 230.2 ± 1.2 Ma. These geochronological and petrological data conclude that the pelitic sediments have experienced a metamorphic event at the Mid–Late Triassic (236.1–218.2 Ma) rather than the Paleoproterozoic (1950–1850 Ma), commonly regarded as the Precambrian basement for the Jiao–Liao–Ji Belt. Hence, the Changhai metamorphic complex should be considered as a discrete lithotectonic group.This newly recognized Mid–Late Triassic metamorphic event (236.1–218.2 Ma) for the Changhai metamorphic complex is coeval with the HP–UHP metamorphic event (235–220 Ma) for Sulu–Dabie rocks. This leads us to speculate that the metamorphism of the Changhai complex belt along the SE margin of the North China Craton was genetically related to the Mid–Late Triassic collision of the North China and South China cratons. By the same token, the Sulu–Dabie HP–UHP Belt may have extended through Yantai, and the southern Yellow Sea, and to the southern side of the Changhai metamorphic complex.     

Evidence for xenolith–host basalt interaction from chemical patterns in Fe–Ti-oxides from mafic granulite xenoliths of the Bakony–Balaton Volcanic field (W-Hungary)

We investigate the effects of xenolith–host basalt interaction on lower crustal mafic granulite xenoliths from the Central Pannonian Basin. The xenoliths are devoid of any signs of melting, nevertheless various phenomena are identified, which indicate that the original mineralogy and chemistry of the xenoliths was modified during interaction with the host basalt. The rock-forming silicates are only slightly affected by alteration, but the Fe–Ti-oxides are overprinted to a significant extent. Complex chemical zoning patterns are detected using high-resolution element mapping in ilmenites and in lamellar titanomagnetite–ilmenite intergrowths. The chemical alteration of the Fe–Ti-oxides was diffusion-controlled and, hence, time and temperature dependent. On the basis of diffusion profiles in titanomagnetite we estimate the duration of xenolith–host basalt interaction to be at least 9–20 h. This is comparable to the time necessary for the ascent of the host basalt to the surface. It is too short to reflect alteration during granulite facies metamorphism in the deep crust. The chemical alteration of the titanomagnetite thus reflects the total duration of the xenolith–host basalt interaction.     

Native Alloys of the Pd–Pt and Ni–Cu–Al Systems from the AS Luna-24

The close intergrowth of two native alloys of the compositions Ni_0.59Cu_0.24Al_0.15Fe_0.01Mn_0.01 and Pd_0.55Pt_0.36Rh_0.09 with a size of 10 μm has been discovered in the regolith from the Mare Crisium. A conclusion on its exhalative origin is made.     

Arsenite removal from water by electro-coagulation on zinc–zinc and copper–copper electrodes

Removal of arsenite from aqueous solution was carried out using electro-coagulation method. The experiments were conducted using copper–copper and zinc–zinc electrodes. The optimized experimental parameters were 2.0 mg/L initial concentration, 16.0-min processing time, 6.0 pH, 3.0-V applied voltage and 30 °C temperature for zinc–zinc electrodes while these values for copper–copper electrodes were 2.0 mg/L initial concentration, 20.0-min processing time, 7.0 pH, 5.0-V applied voltage and 30 °C temperature. The results demonstrated that zinc–zinc and copper–copper electrodes removed arsenite up to 99.89 and 99.56 %, respectively. The treated water was clear, colorless and odorless without any secondary contamination. There was no change in water quality after the removal of arsenite. The reported method is capable to remove arsenite from water at 6–7 pH range, which is a pH range of natural water. Therefore, this method may be the choice of arsenite removal from natural ground water.     

First Record of the Belemnite Genus Hibolithes from Late Jurassic–Early Cretaceous Turbidites from Malaysia

Discovery of the remains of belemnites referred to the Hibolithes sp. from the Jurassic–Cretaceous Pedawan Formation in Sarawak, on the island of Borneo(Malaysia) comprises four fragments of belemnite rostra. The specimens are characterized by multiple fractures and vein filling. Two fragments measuring about 130 mm are relatively intact, with only part of the alveolar region missing; a third piece represents the middle part of a rostrum, and the fourth specimen is too fragmentary to be assigned to any specific part of the rostrum. Based on specimen characteristics, a Tithonian–Hauterivian age is plausible. The sedimentary succession that yielded the belemnite material comprises thick shale that reflects the Te division of Bouma sequence. The occurrence of a Hibolithes taxon in the uppermost Jurassic to lowermost Cretaceous Pedawan Formation sediments in Borneo reflects a near to global palaeobiogeographic distribution of this genus.     

Pb isotope variations in hydrogenetic Fe–Mn crusts from the Izu–Bonin fore-arc

Fe–Mn crusts were recovered from the western escarpment of the Bonin Ridge in the Izu–Bonin fore-arc region (dive site #824: 28.612°N, 141.803°E) at water depths of c. 2900 m using the Shinkai 6500 submersible during cruise YK 04–05. Major and trace element data and XRD mineralogy indicate that the crusts are hydrogenetic in origin. We present profiles of variations in Pb isotope composition measured in-situ by laser ablation MC-ICP-MS across two of the crusts. The isotopic variations are systematic and can be matched up between the two crusts, indicating similar growth rates. The crust Pb isotope composition rules out any local source for Pb from within the Izu–Bonin–Mariana arc system, either from hydrothermal activity or through leaching of volcanic detritus. Input of a globally well-mixed volcanic Pb component, either from aerosols or as an absorbed component on aeolian dust, has been proposed as a mechanism to explain the Pb isotope composition of Central Pacific deep water. However, the Izu–Bonin crusts are displaced to lower ²⁰⁶Pb/²⁰⁴Pb and higher ²⁰⁸Pb/²⁰⁴Pb, which requires an additional Pb source. One possibility is that as water is advected from the south, outboard of the Luzon–Ryukyu–Honshu arc system, it is progressively polluted by Pb derived by weathering and erosion of these young island arc volcanic systems. Using a constant Co-flux model, growth rates are estimated at ～ 7–13 mm/Ma, which would suggest that these crusts provide a record of changes in the composition of deep water in the Izu–Bonin fore-arc region of the western Pacific Ocean over the last 4–8 Ma. Over this interval, the main feature has been a progressive decrease in ²⁰⁷Pb/²⁰⁶Pb (0.843 to 0.839) and ²⁰⁸Pb/²⁰⁶Pb (2.088 to 2.080) with time. The interior parts have compositions similar to those of crusts from the Izu–Bonin fore-arc, while the rims have compositions similar to crusts from the central Western Pacific.     

Genesis of Diamond in Metal–Carbon and Metal–Sulfur–Carbon Melts: Evidence from Experimental Data

Doklady Earth Sciences - The experimental data on diamond growth in the Fe–Ni–S–C and Fe–S–C systems with a sulfur content of 5–14 wt % at 5.5 GPa and...     

Protective mineral layers formed from granite–dry steam interaction

This work focuses on interaction between granite–stainless steel (SUS) pipe–dry steam in the presence of Cu. Three types of hydrothermal experiments were conducted: (1) SUS–Cu–granite, (2) SUS–Cu, (3) SUS–granite. It was found that a high protective amorphous AlSi_1,6O₄ layer (thickness about 5 μm) was formed on the supporting pipe surface only in the case of SUS–Cu–granite interaction. The Al silicate layer formed during the experiment was characterized by X-ray diffraction (XRD) techniques and scanning electron microscopy (SEM) with EDX. According to kinetic data this layer has high protective properties.     

Geochemical modelling of a Zn–Pb skarn: Constraints from LA–ICP–MS analysis of fluid inclusions

The Bismark deposit (northern Chihuahua, Mexico) is one of several base metal-rich high-temperature, carbonate-replacement deposits hosted in northern Mexico. Previous fluid inclusion studies based on microthermometry and PIXE have shown that the Zn-rich, Pb-poor Bismark deposit formed from a moderate salinity magmatic fluid [Baker, T. and Lang, J.R., 2003. Reconciling fluid inclusion types, fluid processes, and fluid sources in skarns: an example from the Bismark Deposit, Mexico. Mineralium Deposita 38(4), 474–495; Baker, T., van Achterberg, E., Ryan, C.G. and Lang, J.R., 2004. Composition and evolution of ore fluids in a magmatic-hydrothermal skarn deposit. Geology 32(2), 117–120]. The exact precipitation mechanisms are unclear and may have due to cooling, salinity decrease and wall rock reaction. Furthermore, PIXE data suggested that Pb and Zn concentrations were comparable and inconsistent with the Zn-rich nature of the ore. However, Pb was commonly below the limit of detection for PIXE and the data presented by Baker et al. [Baker, T., van Achterberg, E., Ryan, C.G. and Lang, J.R., 2004. Composition and evolution of ore fluids in a magmatic-hydrothermal skarn deposit. Geology 32(2), 117–120] are regarded as the maximum concentrations of Pb in the fluid. In this study new LA ICP MS analysis was carried out on the same fluid inclusion population to compare with the PIXE data in order to constrain the uncertainty related to the Pb data and the new results are used to model possible ore deposition mechanisms. The new laser ablation data reveal overall lower concentrations of Pb in the ore fluid (average value ~ 285 ppm) than previously indicated by PIXE analysis (average value ~ 713 ppm). Chemical modelling using the new laser ablation data tested the following ore deposition processes: 1) cooling; 2) fluid–rock reaction at constant temperature; 3) cooling and simultaneous fluid–rock interaction. Modelling results show that the gangue and ore minerals observed at Bismark are best reproduced by fluid–rock interaction and simultaneous cooling. Results from the simulations strongly indicate that ore deposition was mainly driven by a pH increase due to the neutralization of the acidic ore fluid (pH = 3.9) as the result of the reaction with the limestone. Modelling results also suggest that the deposit likely formed under cooling conditions, but do not support the hypothesis of a temperature decrease as the principal ore-forming process.     

Characterisation of aerosol from Santiago,Chile: an integrated PIXE–SEM–EDX study

Santiago de Chile is a big city with huge air quality problems, being one of the most polluted cities in the world. This is aggravated during winter by the topography and meteorological conditions of the city. Although public policies have been developed to minimise the atmospheric aerosol pollution, there is a lack of adequate knowledge and poor characterisation of these aerosols (in its PM_2.5 and PM₁₀ fractions). In this study we sampled atmospheric particles during winter in two distinct areas of Santiago: downtown (Teatinos Street) and in a more residential area (Macul). Major (Si, Al, Fe, Ca and K) and some trace element (S, Cl, Ti, P, Cr, Cu and Zn) compositions were obtained by proton-induced X-ray emission (PIXE). Morphological, type and chemical characterisation was also performed using scanning electron microscopy (SEM) coupled with an energy dispersive X-ray microanalysis system (SEM–EDX). Besides the carbon particles, the contribution of which can be quite important in the atmospheric aerosol, especially in downtown, unambiguously lithogenic (i.e. of geological origin) particles and elements are the second highest contributors. Enrichment factor calculation, together with particle identification and element correlation allow the origin of some elements and particles to be traced, revealing anthropogenic origins for some of them that are specific to the Santiago area.     

Carbonate–Silicate–Sulfide Polyphase Inclusion in Diamond from the Komsomolskaya Kimberlite Pipe,Yakutia

An aragonite inclusion in natural diamond was identified using techniques of transmission electron microscopy, electron microdiffraction, and microprobe analysis. The inclusion is hosted in a colorless octahedral diamond crystal from the Komslomolskaya pipe in Yakutia. The diamond crystal shows a zoned distribution of its admixtures and defects. The structure parameters of the inclusion (∠[001]/[201] = 66° and certain lattice spacings) correspond to the calculated parameters of the orthorhombic unit cell of a Ca carbonate polymorph. The aragonite inclusion contains admixtures of MgO (0.81), MnO (0.58), and FeO (0.13 wt %). The find of a syngenetic aragonite inclusion in diamond is unique and proves that diamond can be formed in carbonatized mantle peridotite at depths of at least 300 km. The inclusion hosts identifiable microphases of Ni-rich sulfides (37–41 wt % Ni), titanite, hydrous silicate, magnetite, and fluid. This association indicates that the diamond and aragonite crystallized from a carbonate–silicate–sulfide melt or highdensity fluid.     

Natural polycomponent solid solutions of the Ru–Os–Ir–Pt–Fe system from the eastern Witwatersrand (South Africa)

This study presents compositional features of platinum-group element mineralization derived from the Late Archaean placers in the eastern part of the Witwatersrand basin. The significant presence of platinum-group minerals, formed by polycomponent solid-solution series in the system Ru–Os–Ir–Pt(±Fe), was determined using an electron microprobe analysis. Compositional data indicate that the source for polycomponent solid solutions of the Ru–Os–Ir–Pt–Fe system was the Archaean mantle of the Earth, slightly differentiated with respect to platinum-group elements.     

Origin of the Yinshan epithermal-porphyry Cu–Au–Pb–Zn–Ag deposit,southeastern China: insights from geochemistry,Sr–Nd and zircon U–Pb–Hf–O isotopes

The Yinshan deposit is a large epithermal-porphyry polymetallic deposit, and the timing and petrogenesis of ore-hosting porphyries have been hotly debated. We present new results from geochemical, whole-rock Sr–Nd and zircon U–Pb–Hf–O isotopic investigations. Zircon U–Pb data demonstrate that the quartz porphyry, dacitic porphyry, and quartz dioritic porphyry formed at ?172.2 ± 0.4 Ma, ?171.7 ± 0.5 Ma, and ?170.9 ± 0.3 Ma, respectively. Inherited zircon cores show significant age spreads from ?730 to ?1390 Ma. Geochemically, they are high-K calc-alkaline or shoshonitic rocks with arc-like trace element patterns. They have similar whole-rock Nd and zircon Hf isotopic compositions, yet an increasing trend in ?_Nd(t) and ?_Hf(t) values typifies the suite. Older (inherited) zircons of the three porphyries display Hf compositions comparable to those of the Jiangnan Orogen basement rocks. In situ zircon oxygen isotopic analyses reveal that they have similar oxygen isotopic compositions, which are close to those of mantle zircons. Moreover, a decreasing trend of δ¹⁸O values is present. We propose that the ore-related porphyries of the Yinshan deposit were emplaced contemporaneously and derived from partial melting of Neoproterozoic arc-derived mafic (or ultra-mafic) rocks. Modelling suggests that the quartz porphyries, dacitic porphyries, and quartz dioritic porphyries experienced ?25%, ?10%, and ?10% crustal contaminations by Shuangqiaoshan rocks. Our study provides important constraints on mantle–crust interaction in the genesis of polymetallic mineralization associated with Mesozoic magmatism in southeastern China.     

Peculiar Mg–Ca–Si metasomatism along a shear zone within the mantle wedge: inference from fine-grained xenoliths from Avacha volcano,Kamchatka

We found extremely high-Mg# (=Mg/(Mg + total Fe) atomic ratio) ultramafic rocks in Avacha peridotite suite. All the high-Mg# rocks have higher modal amounts of clinopyroxene than ordinary Avacha peridotite xenoliths, and their lithology is characteristically heterogeneous, varying from clinopyroxenite through olivine websterite to pyroxene-bearing dunite. The Mg# of minerals is up to 0.99, 0.98 and 0.97 in clinopyroxene, orthopyroxene and olivine, respectively, decreasing progressively toward contact with dunitic part, if any. The petrographical feature of pyroxenes in the high-Mg# pyroxenite indicates their metasomatic origin, and high LREE/HREE ratio of the metasomatic clinopyroxene implies that the pyroxenites are the products of reaction between dunitic peridotites and high-Ca, silicate-rich fluids. The lithological variation of the Avacha high-Mg# pyroxenites from clinopyroxenite to olivine websterite resulted from various degrees of fluid-rock reaction coupled with fractional crystallization of the high-Ca fluids, which started by precipitation of high-Mg# clinopyroxene. Such fluids were possibly generated originally at a highly reduced serpentinized peridotite layer above the subducting slab. The fluids can reach the uppermost mantle along a shear zone as a conduit composed of fine-grained peridotite that developed after continent-ward asthenospheric retreats from the mantle wedge beneath the volcanic front. The fluids are incorporated in mantle partial melts when the magmatism is activated by expansion of asthenosphere to mantle wedge beneath the volcanic front.     

Phycoremediation of cyanide from coke–oven wastewater using cyanobacterial consortium

Owing to the presence of several toxic pollutants such as cyanide, phenol, ammonium, coke–oven wastewater is being considered as hazardous stream and needs to be treated properly. In the present study, cyanobacterial consortium of Dinophysis acuminata and Dinophysis caudata, collected from East Kolkata Wetland, was used for the treatment of both synthetic cyanide solution and real coke–oven wastewater. The growth kinetics was studied considering nitrate as substrate. Since consortium showed growth in cyanide solution, a model was proposed considering both nitrate and cyanide as substrates. The simulated data match quite well with experimental ones. Two coke–oven wastewater samples were collected—untreated one from equalization tank and another from secondary clarifier effluent and treated with consortium separately. Lipid was extracted from biomass of native cyanobacterial consortium, biomass treated with raw coke–oven wastewater and biomass treated with secondary clarifier effluents. Fatty acid methyl ester of such lipid samples was analyzed using gas chromatograph.