Thermodynamic controls on element partitioning between titanomagnetite and andesitic–dacitic silicate melts

Titanomagnetite–melt partitioning of Mg, Mn, Al, Ti, Sc, V, Co, Ni, Cu, Zn, Ga, Zr, Nb, Mo, Hf and Ta was investigated experimentally as a function of oxygen fugacity (fO₂) and temperature (T) in an andesitic–dacitic bulk-chemical compositional range. In these bulk systems, at constant T, there are strong increases in the titanomagnetite–melt partitioning of the divalent cations (Mg²⁺, Mn²⁺, Co²⁺, Ni²⁺, Zn²⁺) and Cu²⁺/Cu⁺ with increasing fO₂ between 0.2 and 3.7 log units above the fayalite–magnetite–quartz buffer. This is attributed to a coupling between magnetite crystallisation and melt composition. Although melt structure has been invoked to explain the patterns of mineral–melt partitioning of divalent cations, a more rigorous justification of magnetite–melt partitioning can be derived from thermodynamic principles, which accounts for much of the supposed influence ascribed to melt structure. The presence of magnetite-rich spinel in equilibrium with melt over a range of fO₂ implies a reciprocal relationship between a(Fe²⁺O) and a(Fe³⁺O_1.5) in the melt. We show that this relationship accounts for the observed dependence of titanomagnetite–melt partitioning of divalent cations with fO₂ in magnetite-rich spinel. As a result of this, titanomagnetite–melt partitioning of divalent cations is indirectly sensitive to changes in fO₂ in silicic, but less so in mafic bulk systems.     

Geothermobarometry on anatectic melts – a high-pressure Variscan migmatite from northeast Sardinia

We studied a high-pressure amphibole-bearing migmatite cropping out along the northeastern coast of Sardinia, a few kilometres northeast of Olbia, in order to improve our knowledge about its evolution using pressure–temperature (P–T) pseudosections. Thermodynamic calculations with PERPLE_X were undertaken in the system Na₂O–K₂O–CaO–FeO–MnO–MgO–Al₂O₃–TiO₂–SiO₂–H₂O using a haplogranitic melt model. Calculations were conducted for average compositions of the protolith and the tonalitic leucosome with different contents of H₂O to construct various pseudosections in the P–T range 2–20 kbar and 550–900°C. We demonstrate that the molar ratios Na/K and Si/Al of the anatectic melt are of high geothermobarometric value. Particularly the melt field in the P–T pseudosection for the protolith, contoured by Si/Al isolines, shows a significant decrease in this ratio with rising pressure. This ratio is only weakly dependent on variable H₂O contents of the amphibole-bearing migmatite as demonstrated by contoured T–H₂O pseudosections. The application of the Na/K and Si/Al ratios in melt yielded P–T conditions close to 13 kbar and 700°C, assigned as the conditions of partial melting. Evaluation of contoured P–T pseudosections for the leucosome composition resulted in conditions of about 10.5 kbar and 700°C for the crystallization of amphibole in the leucosome melt, and 9 kbar and 680°C for complete crystallization of this melt.     

Research on Slope Movement and Landslide by Methods of Analytical Geomechanics

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Different effects of EDTA on uptake and translocation of Pb and Cd by Typha latifolia

Effects of EDTA and heavy metals on growth of Typha latifolia and its uptake and translocation of Pb and Cd were investigated in this study. Both Pb and Cd of high concentrations had inhibitory effect on growth of Typha latifolia. Chlorophyll concentratio…     

Simulating Experiments on Enrichment of Gold by Bacteria and Their Geochemical Significance

The experiments on the enrichment of gold by bacteria indicate that bacteria have a very intense capacity of enriching gold and act as an arrester of trace gold in sea water,Bacteria enrich gold in two forms:absorption and adsorption.Absorption means that gold finds its way into organisms and it is combined with the mercapto group of protein,whereas adsorption means that gold is adsorbed on organisma by amino acid secreted by cell walls,Bacteria are organisms with very high vitality and reproductive capacity and huge productivity in nature Bacteria,which are important geolgical agents for gold enrichment and can exert effects on geological environments by their metabolism,are of important geochemical significance for the formation of gold-bearing black rock series.     

Silicate melts at magmatic temperatures: in-situ structure determination to 1651°C and effect of temperature and bulk composition on the mixing behavior of structural units

The abundance of coexisting structural units in K-, Na-, and Li-silicate melts and glasses from 25° to 1654°C has been determined with in-situ micro-Raman spectroscopy. From these data an equilibrium constant, K_x, for the disproportionation reaction among the structural units coexisting in the melts, Si₂O₅(2Q³)SiO₃(Q²)+SiO₂(Q⁴), was calculated (K_x is the equilibrium constant derived by using mol fractions rather than activities of the structural units). From ln K_x vs l/T relationships the enthalpy (H_x) for the disproportionation reaction is in the range of-30 to 30 kJ/mol with systematic compositional dependence. In the potassium and sodium systems, where the disproportionation reaction shifts to the right with increasing temperature, the H_x increases with silica content (M/Si decreases, M=Na, K). For melts and supercooled liquids of composition Li₂O·2SiO₂ (Li/Si=1), the H_x is indistinguishable from 0. By decreasing the Li/Si to 0.667 (composition LS3) and beyond (e.g., LS4), the disproportionation reaction shifts to the left as the temperature is increased. For a given ratio of M/Si (M=K, Na, Li), there is a positive, near linear correlation between the H_x and the Z/r² of the metal cation. The slope of the H_x vs Z/r² regression lines increases as the system becomes more silica rich (i.e., M/Si is decreased). Activity coefficients for the individual structural units, _i, were calculated from the structural data combined with liquidus phase relations. These coefficients are linear functions of their mol fraction of the form _i=a lnX _i+b, where a is between 0.6 and 0.87, and X _i is the mol fraction of the unit. The value of the intercept, b, is near 0. The relationship between activity coefficients and abundance of individual structural units is not affected by temperature or the electronic properties of the alkali metal. The activity of the structural units, however, depend on their concentration, type of metal cation, and on temperature.     

Determination of retardation coefficients of sulfolane and thiolane on soils by Kow–Koc and solubility parameter, batch and column experiments

 Retardation parameters (R_f) for sulfolane and thioalne were estimated using reference values and experimentally as they were mainly observed at an aquifer underneath a waste disposal site near Brisbane, Australia. Three soil aquifer materials e.g. clay, silty clay and sand were used as sorbents. At first, R_f was obtained employing K_oc–K_ow and solubility parameter, respectively, while experimental coefficients were determined from both batch and flow-through column tests. Additionally, R_f was observed at a single- and bi-solute system through the column test. There was not found any significant difference in R_f between K_oc–K_ow and solubility parameters, but the retardation coefficient was significantly dependent on organic carbon content for solubility parameter. In contrast, using K_oc–K_ow, the coefficient correspondingly varied with an amount of clay content contained in each soil. In the same manner, the batch-determined parameters were more subject to clay content. On the other hand, the column-determined parameters can be comparable with the desk-derived values. In a bi-solute system, they did not influence each other concerning retardation coefficients while they flew though the column simultaneously. It was concluded that there was a large discrepancy in retardation coefficient of batch- against both reference-oriented estimation and column-determined values. Received: 20 August 1998 · Accepted: 17 May 1999     

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.     

The time scales of magma mixing and mingling involving primitive melts and melt–mush interaction at mid-ocean ridges

We have studied the chemical zoning of plagioclase phenocrysts from the slow-spreading Mid-Atlantic Ridge and the intermediate-spreading rate Costa Rica Rift to obtain the time scales of magmatic processes beneath these ridges. The anorthite content, Mg, and Sr in plagioclase phenocrysts from the Mid-Atlantic Ridge can be interpreted as recording initial crystallisation from a primitive magma (~11 wt% MgO) in an open system. This was followed by crystal accumulation in a mush zone and later entrainment of crystals into the erupted magma. The initial magma crystallised plagioclase more anorthitic than those in equilibrium with any erupted basalt. Evidence that the crystals accumulated in a mush zone comes from both: (1) plagioclase rims that were in equilibrium with a Sr-poor melt requiring extreme differentiation; and (2) different crystals found in the same thin section having different histories. Diffusion modelling shows that crystal residence times in the mush were <140 years, whereas the interval between mush disaggregation and eruption was ≤1.5 years. Zoning of anorthite content and Mg in plagioclase phenocrysts from the Costa Rica Rift show that they partially or completely equilibrated with a MgO-rich melt (>11 wt%). Partial equilibration in some crystals can be modelled as starting <1 year prior to eruption but for others longer times are required for complete equilibration. This variety of times is most readily explained if the mixing occurred in a mush zone. None of the plagioclase phenocrysts from the Costa Rica Rift that we studied have Mg contents in equilibrium with their host basalt even at their rims, requiring mixing into a much more evolved magma within days of eruption. In combination these observations suggest that at both intermediate- and slow-spreading ridges: (1) the chemical environment to which crystals are exposed changes on annual to decadal time scales; (2) plagioclase crystals record the existence of melts unlike those erupted; and (3) disaggregation of crystal mush zones appears to precede eruption, providing an efficient mechanism by which evolved interstitial melt can be mixed into erupted basalts.     

Geochemistry of rare high-Nb basalt lavas: Are they derived from a mantle wedge metasomatised by slab melts?

Compositionally, high-Nb basalts are similar to HIMU (high U/Pb) ocean island basalts, continental alkaline basalts and alkaline lavas formed above slab windows. Tertiary alkaline basaltic lavas from eastern Jamaica, West Indies, known as the Halberstadt Volcanic Formation have compositions similar to high-Nb basalts (Nb > 20 ppm). The Halberstadt high-Nb basalts are divided into two compositional sub-groups where Group 1 lavas have more enriched incompatible element concentrations relative to Group 2. Both groups are derived from isotopically different spinel peridotite mantle source regions, which both require garnet and amphibole as metasomatic residual phases. The Halberstadt geochemistry demonstrates that the lavas cannot be derived by partial melting of lower crustal ultramafic complexes, metasomatised mantle lithosphere, subducting slabs, continental crust, mantle plume source regions or an upper mantle source region composed of enriched and depleted components. Instead, their composition, particularly the negative Ce anomalies, the high Th/Nb ratios and the similar isotopic ratios to nearby adakite lavas, suggests that the Halberstadt magmas are derived from a compositionally variable spinel peridotite source region(s) metasomatised by slab melts that precipitated garnet, amphibole, apatite and zircon. It is suggested that high-Nb basalts may be classified as a distinct rock type with Nb > 20 ppm, intraplate alkaline basalt compositions, but that are generated in subduction zones by magmatic processes distinct from those that generate other intraplate lavas.     

Low melt fraction connectivity of granitic and tonalitic melts in a mafic crustal rock at 800 °C and 1 GPa

In the absence of an externally applied stress, the segregation of small amounts of granitic or tonalitic melts from their residual mafic crystals is possible only if the melt forms an interconnected network phase. Accordingly, this research focuses on melt connectivity at low melt fraction (<4 wt% or 5 vol.%). Connectivity of granitic and tonalitic melts in amphibole-rich rock was assessed by performing two types of piston-cylinder experiments at 1 GPa and 800 °C. The first involved annealing samples that consisted of either alternating layers or homogeneous mixtures of calcic amphibole and metaluminous obsidian powder. The second type of experiment involved creating diffusion couples. Here, an upper cylinder of amphibole-saturated granitic or tonalitic melt was placed against a lower cylinder consisting of an amphibole-rich rock containing zero or a small melt (granitic or tonalitic) fraction. The upper part of the diffusion couple was doped with β emitter (¹⁵¹Sm or ¹⁴C) and functioned as an infinite melt reservoir. The lower part of the diffusion couple was considered to be the host rock. The experiments approached textural equilibrium which allowed us to characterize the wetting behaviour of the calcic amphibole by the hydrous silicic melt (granitic or tonalitic). These particular experiments also provided information concerning diffusive transport, because the β emitter could diffuse through the connected melt (liquid) in the amphibole-rich rock. The dihedral angle measurements show that melt connectivity was achieved. This conclusion is based on the fact that the dihedral angles, θ, consistently yielded median apparent values of 53°<θ<58° for an amphibole-rich rock/granitic melt system, and 46°<θ<48° for an amphibole-rich rock/tonalitic melt system. However, the frequency distribution of θ angles is found to be relatively broad. The results of the diffusion-couple experiments, assessed using the β radiographic technique, complement the dihedral (wetting) angle measurements by showing that melt connectivity is achieved at a melt fraction less than 4wt% (5 vol.%). Received: 15 April 1997 / Accepted: 23 September 1998     

Experimental Study on Treatment of High-concentrated Sulfur Wastewater by Process of Depositing Natrojarosite and Its Environmental Significance

High-concentrated sulfur wastewater with sodium and COD （chemical oxygen demand） up to 26000 mg/L from a chemical plant, Jiangsu Province of China has been treated by deposition of natrojarosite in lab. The results indicated that the COD of the wastewater was decreased sharply from 26000 mg/L to 1001 mg/L, with removal rate of COD up to 96% by twice precipitations of natrojarosite and twice oxidation of H202. The treated sulfur wastewater reached the requirement of subsequent biochemical treatment to water quality. The optimal operational parameters should be controlled on pH value between 2.50 and 3.20 and 50 g FeCly6H2O solid added in per liter wastewater. The study provided an experimental basis for pretreatment of high-concentrated sulfur wastewater and proposed a new mineralogical method on treatment of other wastewaters. Depositing process of jarosite and its analogs should be able to be used to treat wastewater from mine and other industries to remove S, Fe and other toxic and harmful elements, such as As, Cr, Hg, Pb, etc. in the water.     

Determination of the effect of Toluene Diisocyanate on mice lung and liver cells by laser confocal microscope

Objective: To detect the effect of TDI on mice lung and liver. Method: Use LCMS with AO dye to analyze the content change of DNA and RNA in mice lung and liver cell induced by different dosages of TDI. Results: Effected at the dosage of 1/4 LC50 and 1/2 L…     

The effects of K2O on the compositions of near-solidus melts of garnet peridotite at 3 GPa and the origin of basalts from enriched mantle

Enrichment in K₂O in oceanic island basalts (OIB) is correlated with high SiO₂, low CaO/Al₂O₃, and radiogenic isotopic signatures indicative of enriched mantle sources (EM1 and EM2). These are also chemical characteristics of the petit-spot lavas, which are highly enriched in K₂O (3–4 wt%) compared to other primitive oceanic basalts. We present experimentally derived liquids with varying concentrations of K₂O in equilibrium with a garnet lherzolite residue at 3 GPa to test the hypothesis that the major element characteristics of EM-type basalts are related to their enrichment in K₂O. SiO₂ is known to increase with K₂O at pressures less than 3 GPa, but it was previously unknown if this effect was significant at the high pressures associated with partial melting at the base of the lithosphere. We find that at 3 GPa for each 1 wt% increase in the K₂O content of a garnet lherzolite saturated melt, SiO₂ increases by ~0.5 wt% and CaO decreases by ~0.5 wt%. MgO and $K_{D}^{{{\text{Fe}} - {\text{Mg}}}}$ K D Fe - Mg each decrease slightly with K₂O concentration, as do Na₂O and Cr₂O₃. The effect of K₂O alone is not strong enough to account for the SiO₂ and CaO signatures associated with high-K₂O OIB. The SiO₂, CaO, and K₂O concentrations of experimentally derived partial melts presented here resemble those of petit-spot lavas, but the Al₂O₃ concentrations from the experimental melts are greater. Partitioning of K₂O between peridotite and melt suggests that petit spots, previously considered to sample ambient asthenosphere, require a source more enriched in K₂O than the MORB source.     

Evidence for Late Miocene to Recent contamination of arc andesites by crustal melts in the Chilean Andes (25–26°S) and its geodynamic implications

Chemical and isotopic data from 12 volcanic centers of the southern Central Volcanic Zone (CVZ) in Chile, whose ages of 20, 16, 11, 8, 5, 2 and <1 Ma bracket the peak of shortening and crustal thickening in the mid-Miocene, show systematic differences with age. The composition of andesites erupted before and after crustal thickening are similar in terms of most major and trace elements, but the post-Miocene andesites show enrichments in Th, U, Cs and Rb, as well as high ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb ratios coupled with low εNd values which indicate greater crustal contamination compared with the older equivalents. Comparison of contamination indicators with age shows that contamination was low from 20 Ma to 8 Ma, increased sharply between 8 and 5 Ma, and remained at a high level into the Quaternary. Constant ratios of fluid-mobile vs immobile elements (Cs/Th or Ba/Zr) in even the most contaminated rocks indicate that fluid interaction was negligible. The contaminated andesites display disequilibrium textures and contain phenocrysts with a mixed population of melt inclusions. We suggest that the main process of crustal contamination was mixing with crustal melts. This is supported by geophysical evidence for a zone of partial melting in the mid and lower crust under the magmatic arc and by the presence of late Miocene to Pliocene crustal-derived felsic ignimbrites in the CVZ.     

Effects of low molecular weight organic acids on sorption and desorption behavior of p-chlorophenol by yellow earth

Low molecular weight organic acids （LMWOAs） are important components of root exudates. They play an important role in immobilizing and remobilizing contaminants in rhizospheric soil. Effects of four LMWOAs on the sorption and desorption behavior of p-chlorophenol by yellow earth was studied in batch mode. The results showed that the previous application of LMWOAs to enhanced adsorption capacity of p-chlorophenol of the soil in the order of maleic acid〉malic acid〉oxalic acid〉citric acid. However, when LMWOAs were applied to soil where p-chlorophenol had been previously adsorbed, substantial p-chlorophenol was desorbed from soil by oxalic acid, whereas citric acid, malic acid and maleic acid didn＇t desorb as much p-chlorophenol from soil as deionized water.     

Early Cretaceous granitoids of the Samarka terrane (Sikhote-Alin’): geochemistry and sources of melts

We present new data on the geologic position, composition, and isotope characteristics of the Early Cretaceous granitoids of the Samarka terrane, Sikhote-Alin’, formed on a transform continental margin. Geological and geochronological data show that these granitoids were generated at two stages of magmatism: in the first half (Hauterivian–Barremian, 130–123 Ma) and second half (Albian–Cenomanian, 110–98 Ma) of the Early Cretaceous. Granitoids of the first stage form an autonomous (free of basic precursors) unimodal melanogranite–granite association and are characterized by normal alkalinity with domination of K over Na, low contents of Ca, and elevated contents of Al₂O₃. By composition, these are S-granites with a model Nd age of ∼1.3 Ga. Granitoids of the second stage are of more diverse petrogeochemical types. They show wider variations in K/Na and A/CNK, are richer in Ca and, sometimes, Sr, and are poorer in P than the granitoids of the first stage. Their compositions form a continuous trend from S- to I-granites, and their model Nd age is ≤1.2 Ga. Comparison of the petrochemical, trace-element, and isotope characteristics of the Early Cretaceous granitoids and upper-crustal rocks (sandstones and siltstones of the turbidite matrix of a Jurassic accretionary prism and basalts from the inclusions in it) of the Samarka terrane and the coeval garrboids has shown that the potassic S-granitoids formed at the early (Hauterivian–Barremian) stage of magmatism as a result of the anatexis of upper-crustal sedimentary rocks. At the late (Albian–Early Cenomanian) stage, the intrusion of mantle magmas led to a temperature increase in the lower crust, which favored more active anatexis, involvement of high-melting substrates (oceanic basalts) in the granite formation, and interaction of mantle and crustal magmas. This resulted in a great diversity of granitoids (from S- to I-type).