首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
Surface complexation models (SCMs) are widely utilized as a tool to study the mobility of radionuclide to the environment. In this study, two SCMs, electrostatic (ES) and non-electrostatic (NES) models are employed in order to simulate the sorption behavior of U(VI) on quartz in the absence of Mg, Ca, and Sr and ES model in the presence of alkaline earth metals. The surface reaction constants (log K) for ES and NES models were fitted to experimental data by coupling PEST with PHREEQC. The SCM prediction of U(VI) sorption on quartz in the absence of alkaline earth metals is in good agreement with the experimental data in the pH range 6.5–9. The estimated log K values are sensitive to both ES and NES model calculations. In U(VI)-Mg-quartz, U(VI)-Ca-quartz, and U(VI)-Sr-quartz systems, only the ES model shows the general trend of the experimental data. The estimated log K values are sensitive with respect to the surface reactions. Hence, the ES model is more suitable for model calculations of the U(VI)-Mg-quartz, U(VI)-Ca-quartz, and U(VI)-Sr-quartz systems.  相似文献   

2.
Recent studies of uranium(VI) geochemistry have focused on the potentially important role of the aqueous species, CaUO2(CO3)32− and Ca2UO2(CO3)30(aq), on inhibition of microbial reduction and uranium(VI) aqueous speciation in contaminated groundwater. However, to our knowledge, there have been no direct studies of the effects of these species on U(VI) adsorption by mineral phases. The sorption of U(VI) on quartz and ferrihydrite was investigated in NaNO3 solutions equilibrated with either ambient air (430 ppm CO2) or 2% CO2 in the presence of 0, 1.8, or 8.9 mM Ca2+. Under conditions where the Ca2UO2(CO3)30(aq) species predominates U(VI) aqueous speciation, the presence of Ca in solution lowered U(VI) adsorption on quartz from 77% in the absence of Ca to 42% and 10% at Ca concentrations of 1.8 and 8.9 mM, respectively. U(VI) adsorption to ferrihydrite decreased from 83% in the absence of Ca to 57% in the presence of 1.8 mM Ca. Surface complexation model predictions that included the formation constant for aqueous Ca2UO2(CO3)30(aq) accurately simulated the effect of Ca2+ on U(VI) sorption onto quartz and ferrihydrite within the thermodynamic uncertainty of the stability constant value. This study confirms that Ca2+ can have a significant impact on the aqueous speciation of U(VI), and consequently, on the sorption and mobility of U(VI) in aquifers.  相似文献   

3.
Uranium(VI) sorption onto kaolinite was investigated as a function of pH (3–12), sorbate/sorbent ratio (1 × 10?6–1 × 10?4 M U(VI) with 2 g/L kaolinite), ionic strength (0.001–0.1 M NaNO3), and pCO2 (0–5%) in the presence or absence of 1 × 10?2–1 × 10?4 M citric acid, 1 × 10?2–1 × 10?4 M EDTA, and 10 or 20 mg/L fulvic acid. Control experiments without-solids, containing 1 × 10?6–1 × 10?4 M U(VI) in 0.01 M NaNO3 were used to evaluate sorption to the container wall and precipitation of U phases as a function of pH. Control experiments demonstrate significant loss (up to 100%) of U from solution. Although some loss, particularly in 1 × 10?5 and 1 × 10?4 M U experiments, is expected due to precipitation of schoepite, adsorption on the container walls is significant, particularly in 1 × 10?6 M U experiments. In the absence of ligands, U(VI) sorption on kaolinite increases from pH ～3 to 7 and decreases from pH ～7.5 to 12. Increasing ionic strength from 0.001 to 0.1 M produces only a slight decrease in U(VI) sorption at pH < 7, whereas 10% pCO2 greatly diminishes U(VI) sorption between pH ～5.5 and 11. Addition of fulvic acid produces a small increase in U(VI) sorption at pH < 5; in contrast, between pH 5 and 10 fulvic acid, citric acid, and EDTA all decrease U(VI) sorption. This suggests that fulvic acid enhances U(VI) sorption slightly via formation of ternary ligand bridges at low pH, whereas EDTA and citric acid do not form ternary surface complexes with the U(VI), and that all three ligands, as well as carbonate, form aqueous uranyl complexes that keep U(VI) in solution at higher pH.  相似文献   

4.
This study reports on the seepage of metals, metalloids and radionuclides from the Mary Kathleen uranium mill tailings repository. Since rehabilitation in the 1980s, the capped tailings have developed a stratified hydrochemistry, with acid (pH 3.7), saline, metal-rich (Fe, Mn, Ni, U ± As, Pb, Zn), oxygenated (1.05 mg L−1 DO), radioactive waters in the upper tailings pile and near-neutral pH (pH 7.57), metal-poor, reduced (0.08 mg L−1 DO) waters at depth. Seepage (∼0.5 L s−1) of acid (pH 5.5), metal-rich (Fe, Mn ± Ni, U, Zn), radioactive (U-235, U-238, Ra-226, Ra-228, Ac-227) waters occurs from the base of the tailings dam retaining wall into the former evaporation pond and local drainage system. Oxygenation of the seepage waters causes the precipitation of Fe and coprecipitation and adsorption of other metals (U, Y), metalloids (As), rare earth elements (Ce, La) and radionuclides (U-235, U-238). By contrast, alkalis and alkaline–earth elements (Ca, K, Mg, Na, Sr), Mn, sulfate and to some degree metals (U, Zn, Ni), rare earth elements (Ce, La) and radionuclides (U-235, U-238, Ra-226, Ra-228) remain in solution until pH neutralisation and evaporation lead to their precipitation in efflorescences and sulfate-rich evaporative sediments. While the release of contaminant loads from the waste repository through seepage is insignificant (e.g. ∼5 kg of U per year), surface waters downstream of the tailings impoundment possess TDS, U and SO4 concentrations that exceed Australian water quality guideline values in livestock drinking water. Thus, in areas with a semi-arid climate, even insignificant load releases of contaminants from capped tailings repositories can still cause the deterioration of water quality in ephemeral creek systems.  相似文献   

5.
We investigate the sensitivity of U/Ca, Mg/Ca, and Sr/Ca to changes in seawater [CO32−] and temperature in calcite produced by the two planktonic foraminifera species, Orbulina universa and Globigerina bulloides, in laboratory culture experiments. Our results demonstrate that at constant temperature, U/Ca in O. universa decreases by 25 ± 7% per 100 μmol [CO32−] kg−1, as seawater [CO32−] increases from 110 to 470 μmol kg−1. Results from G. bulloides suggest a similar relationship, but U/Ca is consistently offset by ∼+40% at the same environmental [CO32−]. In O. universa, U/Ca is insensitive to temperature between 15°C and 25°C. Applying the O. universa relationship to three U/Ca records from a related species, Globigerinoides sacculifer, we estimate that Caribbean and tropical Atlantic [CO32−] was 110 ± 70 μmol kg−1 and 80 ± 40 μmol kg−1 higher, respectively, during the last glacial period relative to the Holocene. This result is consistent with estimates of the glacial-interglacial change in surface water [CO32−] based on both modeling and on boron isotope pH estimates. In settings where the addition of U by diagenetic processes is not a factor, down-core records of foraminiferal U/Ca have potential to provide information about changes in the ocean’s carbonate concentration.Below ambient pH (pH < 8.2), Mg/Ca decreased by 7 ± 5% (O. universa) to 16 ± 6% (G. bulloides) per 0.1 unit increase in pH. Above ambient pH, the change in Mg/Ca was not significant for either species. This result suggests that Mg/Ca-based paleotemperature estimates for the Quaternary, during which surface-ocean pH has been at or above modern levels, have not been biased by variations in surface-water pH. Sr/Ca increased linearly by 1.6 ± 0.4% per 0.1 unit increase in pH. Shell Mg/Ca increased exponentially with temperature in O. universa, where Mg/Ca = 0.85 exp (0.096*T), whereas the change in Sr/Ca with temperature was within the reproducibility of replicate measurements.  相似文献   

6.
Geochemical evolution of uraniferous soda lakes in Eastern Mongolia   总被引：1，自引：1，他引：0  
Extremely high concentrations of uranium (U) were discovered in shallow, groundwater-fed hyperalkaline soda lakes in Eastern Mongolia. A representative groundwater sample in this area is dilute and alkaline, pH = 7.9, with 10 mM TIC and 5 mM Cl−. In contrast, a representative lake water sample is pH ~ 10 with TIC and Cl− each more than 1,000 mM. Groundwater concentrations of U range from 0.03 to 0.43 μM L−1. Lake water U ranges from 0.24 to >62.5 μM, possibly the highest naturally occurring U concentrations ever reported in surface water. Strontium isotopes 87Sr/86Sr varied in groundwaters from 0.706192 to 0.709776 and in lakes 87Sr/86Sr varied from 0.708702 to 0.709432. High concentrations of U, Na, Cl−, and K correlate to radiogenic Sr in lake waters suggesting that U is sourced from local Cretaceous alkaline rhyolites. Uranium-rich groundwaters are concentrated by evaporation and U(VI) is chelated by CO3−2 to form the highly soluble UO2(CO3)3−4. Modeled evaporation of lakes suggests that a U-mineral phase is likely to precipitate during evaporation.  相似文献   

7.
The carbonates, clays and major chemical compositions of lacustrine sediments in Nam Co (Lake) were examined by X-ray diffraction, scanning electron microscopy and chemical analysis. Carbonates include monohydrocalcite (MHC, first report from China and in a high-altitude lake), low-Mg calcite and traces of dolomite. MHC in Nam Co is developed in water (1.8 g/L) with high Mg/Ca molar ratios (10.03–15.03), high pH (8.04–9.72) and the presence of bacteria, algae, diatom and ostracoda. Illite and Mg-chlorite provide a strong evidence for physical weathering in the Holocene. Most Ca and Sr in sediments originate from carbonates as the molar ratios of Ca and CO32− are all less than 1 and the curve of Sr is very similar to that of Ca. However, most of the Mg, Fe and Rb are from clays. The lake water shifted from a fresh water environment to an evaporative, alkaline environment by 2.06 cal. ka BP. There was a depositional event that the depositional rate changed from 0.134 to 1.639 mm/a at about 2 cal. ka BP.  相似文献   

8.
Migration of uranium and arsenic in aquatic environments is often controlled by sorption on minerals present along the water flow path. To investigate the sorption behaviour, batch experiments were conducted for uranium and arsenic as single components and also solutions containing both uranium and arsenic in the presence of SiO2, Al2O3, TiO2 and FeOOH at a pH ranging from 3 to 9. In solutions containing only U(VI) or As(V) with the minerals, the sorption of U(VI) was low at acidic pH range and increases with increasing pH, whereas As(V) showed opposite sorption behaviour to Al2O3, TiO2 and FeOOH from acidic pH range to alkaline condition. For the As(V)–SiO2 system, the sorption was low for almost all pH. Sorption of U(VI) and As(V) on SiO2 and FeOOH is almost similar in solutions containing either U(VI) or As(V) separately, or both together. In the U(VI)–As(V)–Al2O3 system, a significant retardation in uranyl sorption and an enhancement in arsenate sorption on Al2O3 were observed for a wide range of pH. The sorption behaviour of U(VI) and As(V) was changed when Al2O3 was replaced by TiO2, where an increase in sorption was observed for both elements. The sorption behaviour of uranyl and arsenate in the U(VI)–As(V)–TiO2 system gives evidence for the formation of uranyl–arsenate complexes. The change in sorption retardation/enhancement of U(VI) and As(V) could be explained by the formation of uranyl–arsenate complexes or due to the competitive sorption between uranyl and arsenate species.  相似文献   

9.
Sr/Ca, B/Ca, Mg/Ca and δ11B were determined at high spatial resolution across ∼1 year of a modern Hawaiian Porites lobata coral by secondary ion mass spectrometry (SIMS). We observe significant variations in B/Ca, Mg/Ca, Sr/Ca and δ11B over short skeletal distances (nominally equivalent to periods of <20 days). This heterogeneity probably reflects variations in the composition of the extracellular calcifying fluid (ECF) from which the skeleton precipitates. Calcification site pH (total scale) was estimated from skeletal δ11B and ranged from 8.3 to 8.8 (± ∼0.1) with a mean of ∼8.6. Sr/Ca and B/Ca heterogeneity is not simply correlated with calcification site pH, as might be expected if Ca-ATPase activity increases the pH and decreases the Sr/Ca and B(OH)4−/CO32− ratios of the ECF. We produced a simple model of the ECF composition and the skeleton deposited from it, over a range of calcium transport and carbonate scenarios, which can account for these observed geochemical variations. The relationship between the pH and Sr/Ca of the ECF is dependent on the concentration of DIC at the calcification site. At higher DIC concentrations the ECF has a high capacity to buffer the [H+] changes induced by Ca-ATPase pumping. Conversely, at low DIC concentrations, this buffering capacity is reduced and ECF pH changes more rapidly in response to Ca-ATPase pumping. The absence of a simple correlation between ECF pH and skeletal Sr/Ca implies that calcification occurred under a range of DIC concentrations, reflecting variations in the respiration and photosynthesis of the coral and symbiotic zooxanthellate in the overlying coral tissues. Our observations have important implications for the use of coral skeletons as indicators of palaeo-ocean pH.  相似文献   

10.
17O NMR shieldings are calculated for the central O in the molecular model OM6(OH)12 –2, for crystalline alkaline earth oxides, MO, where M=Mg, Ca, and Sr, using both Hartree–Fock and hybrid Hartree–Fock density-functional theory. Agreement of calculated and experimental NMR shifts of CaO and SrO compared to MgO is good, but only if the basis set on the M atoms has sufficient tight d polarization functions. Preliminary results are also presented for nonbridging O in the silicate Si(OH)3O– anion, perturbed by alkaline earth cations, giving trends which agree qualitatively with experiment.  相似文献   

11.
X-ray diffraction (XRD), back scattered electron imaging (BSE), wavelength-dispersion spectral scan (WDS), X-ray compositional mapping and quantitative electron probe micro analyses (EPMA) have been used to examine a natural attenuation of U during low temperature alteration of the Sela granite, south Eastern Desert of Egypt. The data confirmed that a pre-existing hydroxyapatite was transformed to autunite through an unidentified intermediate phase. The boundaries between these three phases are not sharp and are generally interfering indicative of the replacement of Ca by U. The hydroxyapatite, intermediate phase and autunite show similar chondrite normalized rare earth elements (REE) patterns suggesting a genetic relationship. Alteration processes have enriched the three phases with heavy rare earth elements (HREE) and Eu and caused Ce, Dy and Yb negative anomalies. Based on the pH of the aqueous solutions, two mechanisms may explain the conversion of hydroxyapatite to autunite: (1) the dissolution of hydroxyapatite and precipitation of autunite which would happen when the uranyl bearing solutions were acidic enough (pH = 3–6.8) to be able to dissolve the pre-existing hydroxyapatite and (2) sorption of the uranyl ion on the surface of hydroxyapatite followed by substitution of (UO2)2+ at the expense of Ca2+. The latter mechanism would have happened if the pH of the aqueous solutions were near neutral and at low dissolved concentrations of uranyl ion. The genesis of uranyl mineralization in the Sela area supports the use of apatite-based technologies for U remediation in an oxidizing environment.  相似文献   

12.
Geochronological, geochemical and whole-rock Sr–Nd isotopic analyses have been completed on a suite of alkaline ultramafic dykes from southwest (SW) Guizhou Province, China with the aim of characterising their petrogenesis. The Baiceng ultramafic dykes have a LA-ICP-MS zircon 206Pb/238U age of 88.1 ± 1.1 Ma (n = 8), whereas two phlogopites studied by 40Ar/39Ar dating methods give emplacement ages of 85.25 ± 0.57 Ma and 87.51 ± 0.45 Ma for ultramafic dykes from Yinhe and Lurong, respectively. In terms of composition, these Late Mesozoic ultramafic dykes belong to the alkaline magma series due to their high K2O (3.31–5.04 wt.%) contents. The dykes are characterised by enrichment of light rare earth element (LREE) and large-ion lithosphile elements (LILEs) (Rb and Ba), negative anomalies in high field strength elements (HFSEs), such as, Nb, Ta and Ti relative to primitive mantle, low initial 87Sr/86Sr ratios (0.7060–0.7063) and positive εNd(t) values (0.3–0.4). Such features suggest derivation from low degree (< 1%) partial melting of depleted asthenospheric mantle (garnet-lherzolite), and contamination to various degrees (～ 10%) by interaction with upper crustal materials.  相似文献   

13.
《Resource Geology》2018,68(1):1-21
The Daheishan Mo deposit of the Lesser Xing'an–Zhangguangcai Range metallogenic belt in northeast China is a super‐large molybdenum deposit with Mo reserves of 1.09 Mt. The Mo mineralization occurs mainly in a granodiorite porphyry. Zircon SIMS U–Pb dating yields a crystallization age of 168.3 ± 1.4 Ma for the granodiorite porphyry. Molybdenite Re–Os dating indicates that Mo mineralization occurred at 169.2 ± 1.2 Ma. These geochronological data indicate that these magmatic and hydrothermal activities occurred during the Middle Jurassic. The granodiorite porphyry can be classified as high‐K calc‐alkaline series, and the rare earth elements (REE) are characterized by a significant fractionation between light REE (LREE) and heavy REE (HREE) with slightly positive Eu anomalies (Eu/Eu* = 1.08–1.12). Large ion lithophile elements (e.g., Rb, U, K, and Pb) are enriched, whereas high field strength elements (e.g., Nb, Ta, Ti, HREEs, and Yb) are strongly depleted. The granodiorite porphyry is also characterized by initial strontium isotope ratios (87Sr/86Sr)i of 0.70460–0.70482 and magmatic zircon δ18O values of 5.2–6.5 ‰ that are similar to those of the mantle. Zircon ɛHf(t) and whole‐rock ε Nd(t) values range from 5.6 to 9.9 and 0.8 to 1.1, respectively. The two‐stage Nd model ages (TDM2) are in the range of 868–894 Ma, similar to Hf model ages, indicating that the parent magma has a uniform source and primarily originated from a juvenile crustal source. Combined with the regional geological history, geochemistry of the Daheishan granodiorite porphyry, and new isotopic age data, we propose that the formation of the Daheishan porphyry Mo deposit is likely related to the subduction of the Paleo‐Pacific Plate.  相似文献   

14.
We have developed a rapid and precise procedure for measuring multiple elements in foraminifera and corals by inductively coupled plasma sector field mass spectrometry (ICP-SF-MS) with both cold- [800 W radio frequency (RF) power] and hot- (1200 W RF power) plasma techniques. Our quality control program includes careful subsampling protocols, contamination-free workbench spaces, and refined plastic-ware cleaning process. Element/Ca ratios are calculated directly from ion beam intensities of 24Mg, 27Al, 43Ca, 55Mn, 57Fe, 86Sr, and 138Ba, using a standard bracketing method. A routine measurement time is 3–5 min per dissolved sample. The matrix effects of nitric acid, and Ca and Sr levels, are carefully quantified and overcome. There is no significant difference between data determined by cold- and hot-plasma methods, but the techniques have different advantages. The cold-plasma technique offers a more stable plasma condition and better reproducibility for ppm-level elements. Long-term 2-sigma relative standard deviations (2-RSD) for repeat measurements of an in-house coral standard are 0.32% for Mg/Ca and 0.43% for Sr/Ca by cold-plasma ICP-SF-MS, and 0.69% for Mg/Ca and 0.51% for Sr/Ca by hot-plasma ICP-SF-MS. The higher sensitivity and enhanced measurement precision of the hot-plasma procedure yields 2-RSD precision for μmol/mol trace elements of 0.60% (Mg/Ca), 9.9% (Al/Ca), 0.68% (Mn/Ca), 2.7% (Fe/Ca), 0.50% (Sr/Ca), and 0.84% (Ba/Ca) for an in-house foraminiferal standard. Our refined ICP-SF-MS technique, which has the advantages of small sample size (2–4 μg carbonate consumed) and fast sample throughput (5–8 samples/hour), should open the way to the production of high precision and high resolution geochemical records for natural carbonate materials.  相似文献   

15.
《Applied Geochemistry》2002,17(4):399-408
The sorption of U(VI) onto the surface of olivine has been experimentally investigated at 25 °C under an air atmosphere as a function of pH, solid surface to volume ratio and total U concentration. Sorption has been observed to decrease as the extent of carbonate complexation of U(VI) in solution increases, which is attributed to the competition between aqueous and solid ligands for the coordination of U. The experimental results have been interpreted by means of two different approaches: (1)a semi-empirical model, exemplified by the application of a Langmuir isotherm and (2) a non-electrostatic thermodynamic surface complexation model which includes the formation of the surface species: >SO–UO2+ and >SO–UO2(OH). The following stability constants for these species have been determined from the thermodynamic analysis: K(>SO–UO2+)=289±71 and K(>SO–UO2(OH))=(3.4±0.4)×10−6. The comparison of the sorption of U onto olivine with granites of different origin indicate that the use of this mineral as additive to the backfill of deep high level nuclear waste repositories could retard the migration of U from the repository to the geosphere.  相似文献   

16.
A mixing of metal-loaded acid mine drainage with shallow groundwater or surface waters usually initiates oxidation and/or hydrolysis of dissolved metals such as iron (Fe) and aluminum (Al). Colloidal particles may appear and agglomerate with increasing pH. Likewise chemical conditions may occur while flooding abandoned uranium mines. Here, the risk assessment of hazards requires reliable knowledge on the mobility of uranium (U). A flooding process was simulated at mesocosm scale by mixing U-contaminated acid mine water with near-neutral groundwater under oxic conditions. The mechanism of U-uptake by fresh precipitates and the molecular structure of U bonding were determined to estimate the mobility of U(VI). Analytical and spectroscopic methods such as Extended X-ray Absorption Fine-Structure (EXAFS) spectroscopy at the Fe K-edge and the U LIII-edge, and Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) spectroscopy were employed. The freshly formed precipitate was identified as colloidal two-line ferrihydrite. It removed U(VI) from solution by sorption processes, while surface precipitation or structural incorporation of U was not observed. EXAFS data suggest a mononuclear inner-sphere, edge-sharing complex of U(VI) with ferrihydrite in the absence of dissolved carbonate. By employing a novel EXAFS analysis method, Monte Carlo Target Transformation Factor Analysis, we could for the first time ascertain a 3-D configuration of this sorption complex without the necessity to invoke formation of a ternary complex. The configuration suggests a slightly tilted position of the adsorbed unit relative to the edge-sharing Fe(O, OH)6 octahedra. In the presence of dissolved carbonate and at pH ∼8.0, a distal carbonate O-atom at ∼4.3 Å supports formation of ternary U(VI)-carbonato surface complexes. The occurrence of these complexes was also confirmed by ATR-FTIR. However, in slightly acidic conditions (pH 5-6) in equilibrium with atmospheric CO2, the U(VI) sorption on ferrihydrite was dominated by the binary complex species Fe(O)2UO2, whereas ternary U(VI)-carbonato surface complexes were of minor relevance. While sulfate and silicate were also present in the mine water, they had no detectable influence on U(VI) surface complexation. Our experiments demonstrate that U(VI) forms stable inner-sphere sorption complexes even in the presence of carbonate and at slightly alkaline pH, conditions which previously have been assumed to greatly accelerate the mobility of U(VI) in aqueous environments. Depending on the concentrations of U(VI) and carbonate, the type of surface complexes may change from binary uranyl-ferrihydrite to ternary carbonato-uranyl-ferrihydrite complexes. These different binding mechanisms are likely to influence the binding stability and retention of U(VI) at the macroscopic level.  相似文献   

17.
Given the relevance of desert aerosols to environmental issues such as dust storms, climate change and human health effects, we provide a demonstration of how the bedrock geology of an arid area influences the mineralogy and geochemistry of even the finest particulate matter (i.e., the inhalable fraction <10 μm in size: PM10). PM10 samples extracted from desert sediments at geologically contrasting off-road sites in central and southeastern Australia (granitic, high grade metamorphic, quartzitic sandstone) were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS). The “granitic” PM10 are highly alkali feldspathic and illitic, with a wide range of accessory minerals including rutile (TiO2), monazite [(Ce, La, Nd, Th, Y) PO4], xenotime (YPO4), apatite [Ca5(PO4)3 (F, OH, Cl)], hematite (Fe3O4), zircon (ZrSiO4) and thorite (ThSiO4). This mineralogy is reflected in the geochemistry which shows notable enrichments in rare earth elements (REE) and most high field strength elements (both held in the accessory minerals), and higher than normal levels of low (<2.0) ionic potential elements (Na, K, Li, Cs, Rb: held in alkali feldspar and illite). The “metamorphic” resuspended PM10 define a mineralogy clearly influenced by local exposures of pelitic and calc-silicate schists (sillimanite, muscovite, calcite, Ca-amphibole), a dominance of monazite over other REE-bearing phases, and a geochemistry distinguished by enrichments in alkaline earth metals (Ca, Mg, Ba, Sr) and depletion in heavy REE. The “quartzite” PM10, derived from rocks already recycled by Precambrian erosion and sedimentary transport, show a sedimentologically mature mineralogy of mostly quartz and kaolinite, detrital accessory ilmenite, rutile, monazite and hematite, and the strongest geochemical depletion (especially K, Rb, Cs, Na, Ca, Mg, Ba).  相似文献   

18.
This study presents new geochronological and geochemical data for Early Cretaceous volcanic rocks in the southern margin of the North China Craton (NCC), to discuss the crust–mantle interaction. The studied rocks include pyroxene andesites from Daying Formation, hornblende andesites and andesites from Jiudian Formation, and rhyolites from a hitherto unnamed Formation. These rocks formed in Early Cretaceous (138–120 Ma), with enrichment in light rare earth elements (REE), depletion in heavy REE and arc-like trace elements characteristics. Pyroxene andesites show low SiO2 contents and enriched Sr–Nd–Pb–Hf isotopic compositions, with orthopyroxene phenocryst and Paleoproterozoic (2320–1829 Ma) inherited zircons, suggesting that they originated from lithospheric mantle after metasomatism with NCC lower crustal materials. Hornblende andesites have low SiO2 contents and high Mg# (Mg# = 100 Mg/(Mg + Fe2+)) values, indicating a lithospheric-mantle origin. Considering the distinct whole-rock Sr isotopic compositions we divide them into two groups. Among them, the low (87Sr/86Sr)i andesites possess amount inherited Neoarchean to Neoproterozoic (2548–845 Ma) zircons, indicating the origin of lithospheric mantle with addition of Yangtze Craton (YC) and NCC materials. In comparison, the high (87Sr/86Sr)i andesites, with abundant Neoarchean–Paleozoic inherited zircons (3499–261 Ma), are formed by partial melting of lithospheric mantle with incorporation of NCC supracrustal rocks and YC materials. Rhyolites have extremely high SiO2 (77.63–82.52 wt.%) and low total Fe2O3, Cr, Ni contents and Mg# values, combined with ancient inherited zircon ages (2316 and 2251 Ma), suggesting an origin of NCC lower continental crust. Considering the presence of resorption texture of quartz phenocryst, we propose a petrogenetic model of ‘crystal mushes’ for rhyolites prior to their eruption. These constraints record the intense crust–mantle interaction in the southern margin of the NCC. Given the regional data and spatial distribution of Early Cretaceous rocks within NCC, we believe that the formation of these rocks is related to the contemporaneous far-field effect of the Paleo-Pacific Plate.  相似文献   

19.
Alkaline intrusions in the eastern Shandong Province consist of quartz monzonite and granite. U-Pb zircon ages, geochemical data, and Sr-Nd-Pb isotopic data for these rocks are reported in the present paper. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U-Pb zircon analyses yielded consistent ages ranging from 114.3?±?0.3 to 122.3?±?0.4 Ma for six samples of the felsic rocks. The felsic rocks are characterised by a wide range of chemical compositions (SiO2?=?55.14–77.63 wt. %, MgO?=?0.09–4.64 wt. %, Fe2O3?=?0.56–7.6 wt. %, CaO?=?0.40–5.2 wt. %), light rare earth elements (LREEs) and large ion lithophile elements (LILEs) (i.e., Rb, Pb, U) enrichment, as well as significant rare earth elements (HREEs) and heavy field strength (HFSEs) (Nb, Ta, P and Ti) depletion, various and high (87Sr/86Sr) i ranging from 0.7066 to 0.7087, low ε Nd (t) values from ?14.1 to ?17.1, high neodymium model ages (TDM1?=?1.56–2.38Ga, TDM2?=?2.02–2.25Ga), 206Pb/204Pb?=?17.12–17.16, 207Pb/204Pb?=?15.44–15.51, and 208Pb/204Pb?=?37.55–37.72. The results suggested that these rocks were derived from an enriched crustal source. In addition, the alkaline rocks also evolved as the result of the fractionation of potassium feldspar, plagioclase, +/? ilmenite or rutile and apatite. However, the alkaline rocks were not affected by crustal contamination. Moreover, the generation of the alkaline rocks can be attributed to the structural collapse of the Sulu organic belt due to various processes.  相似文献   

20.
With the aim of constraining the Early Mesozoic tectonic evolution of the eastern section of the Central Asian Orogenic Belt (CAOB), we undertook zircon U–Pb dating and geochemical analyses (major and trace elements, Sr–Nd isotopes) of volcanic rocks of the Luoquanzhan Formation and Daxinggou Group in eastern Heilongjiang and Jilin provinces, China. The analyzed rocks consist mainly of dacite and rhyolite, with SiO2 contents of 68.52–76.65 wt%. Three samples from the Luoquanzhan Formation and one from the Daxinggou Group were analyzed using laser ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS) U–Pb zircon techniques. Three zircons with well-defined oscillatory zoning yielded weighted mean 206Pb/238U ages of 217 ± 1, 214 ± 2, and 208 ± 1 Ma, and one zircon with oscillatory zoning yielded a weighted mean 206Pb/238U age of 201 ± 1 Ma. These ages are interpreted to represent the timing of eruption of the volcanic rocks. The Triassic volcanic rocks are characterized by high SiO2 and low MgO concentrations, enrichment in large ion lithophile elements (LILEs) and light rare earth elements (LREEs), depletion in high field strength elements (HFSEs) and heavy rare earth elements (HREEs), (87Sr/86Sr)i = 0.7040–0.7050 (Luoquanzhan Formation) and 0.7163–0.7381 (Daxinggou Group), and εNd (t) = 1.89–3.94 (Luoquanzhan Formation) and 3.42–3.68 (Daxinggou Group). These geochemical features indicate an origin involving the partial melting of juvenile lower crust (Nd model ages (TDM2) of 651–821 Ma) and that compositional variation among the volcanic rocks arose from mineral fractionation and minor assimilation. These volcanic rocks formed within an extensional environment following collision of the NCC and Jiamusi-Khanka Massif during the Late Paleozoic–Early Triassic.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号