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1.
To investigate the possible variations of Rn concentration in crystalline rocks as a function of flow conditions, a field study was carried out of a fractured aquifer in granite. The method is based on the in situ measurement of Rn in groundwater, aquifer tests for the determination of hydraulic characteristics of the aquifer and laboratory measurement of Rn exhalation rate from rocks. A simple crack model that simulates the Rn concentration in waters circulating in a fracture intersecting a borehole was also tested. The Rn concentrations in groundwaters from boreholes of the study site ranged from 192 to 1597 Bq L−1. The Rn exhalation rates of selected samples of granite and micaschist were determined from laboratory experiments. The results yielded fluxes varying from 0.5 to 1.3 mBq m−2 s−1 in granite and from 0.5 to 0.9 mBq m−2 s−1 in micaschists. Pumping tests were performed in the studied boreholes to estimate the transmissivity and calculate the equivalent hydraulic aperture of the fractures. Transmissivities ranged from 10−5 to 10−3 m2 s−1. Using the cubic law, hydraulic equivalent fracture apertures were calculated to be in the range of 0.5–2.3 mm.  相似文献   

2.
Ten highly weathered soils in southeastern Nigeria were sampled from their typical A and B horizons for analyses. The objectives were to determine the different forms of Fe and Al oxides in the soils and relating their occurrence to phosphate availability and retention in the soils. The soils are deep and often physically degraded but are well drained and coarse in the particle size distribution. They are mostly dominated by kaolinite in their mineralogy with very high values of SiO2. The soils are acidic with low soil organic carbon (SOC) contents. The elements in the exchange complex are also low thus reflecting in the low CEC of the soil. Available phosphorus (P) in the soils are generally low while total P ranged from 157 to 982 mg kg−1 with an overall average of 422 mg kg−1. Total Fe in the soil is highest and their order represented as follows: Fet > Fed > Feox ≥ Fep. The pyrophosphate extractable Fe was always higher in the top soil than in the subsoil and was attributed to the fact that these forms of Fe are associated with organic matter which is more abundant in topsoil than in subsoil. Like in Fe forms, the order of Al occurrence could generally be presented as; Alt > Ald > Alox > Alp. More Fe and Al oxides in the soils are strongly crystalline while a small quantity is poorly crystalline Fe forms. The amorphous forms of both Fe and Al are very low in the soils when compared with the crystalline forms. The oxides that show very strong affinity to total P are Fed–Feox, Fed, Ald, Fet, Feox and Alox/Ald. To overcome this problem of P retention in the soil, we recommend constant liming of these soils to neutralize them, application of organic matter and of high dosage of phosphate fertilizer to the soils.  相似文献   

3.
To understand the geochemical cycle of Hg in hypereutrophic freshwater lake, two sampling campaigns were conducted in Lake Taihu in China during May and September of 2009. The concentrations of unfiltered total Hg (unfTHg) were in the range of 6.8–83 ng L−1 (28 ± 18 ng L−1) in the lake water and total Hg in the sediment was 12–470 ng g−1, both of which are higher than in other background lakes. The concentration of unfTHg in ∼11% of the lake water samples exceeded the second class of the Chinese environmental standards for surface water of 50 ng L−1 (GB 3838-2002), indicating that a high ecological risk is posed by the Hg in Lake Taihu. However, the concentrations of unfiltered total MeHg (unfMeHg) were relatively low in the lake water (0.14 ± 0.05 ng L−1, excluding two samples with 0.81 and 1.0 ng L−1). Lake sediment MeHg varied from 0.2–0.96 ng g−1, with generally low ratios of MeHg/THg of <1%. The low concentrations of TMeHg in the lake water may have resulted from a strong uptake by the high primary productivity and the demethylation of MeHg in oxic conditions. In addition, contrary to the results of previous research conducted in deep-water lakes and reservoirs, the low concentrations of MeHg and low ratio of MeHg/THg in the lake sediment indicates that the net methylation of Hg was not accelerated by the elevated organic matter load created by the eutrophication of Lake Taihu. The results also showed that sediments were a source of THg and MeHg in the water. Higher diffusion fluxes of THg and MeHg may be partly responsible for the higher concentrations of THg in the lake water in May, 2009.  相似文献   

4.
239 + 240Pu activities of 100–450dpm/kg are found down to 15–18 cm in anoxic Saanich Inlet sediments, with a subsurface maximum in undisturbed deposits. Integrated 239 + 240Pu inventories which overlap delivery estimates are present both in two cores of anoxic sediments from Saanich Inlet and in one core of oxic sediments 65 km away in Dabob Bay, Washington. 241Am239 + 240Pu ratios in Saanich Inlet sediments overlap ratios in unfractionated midnorthern latitude fallout, in oxic sediments from the Washington continental shelf, and in anoxic sediments from two basins off southern California and Mexico. The 239 + 240Pu137Cs ratios in three intervals of Saanich Inlet sediments are also in agreement with ratios previously reported for oxic coastal marine sediments. The Pu inventories, the AmPu and PuCs ratios, and the Saanich Inlet Dabob Bay comparison all argue that Pu is not rapidly remobilized in anoxic sediments.The subsurface 239 + 240Pu activity maximum is not in agreement with the historical record of peak Pu fallout in 1963–1964 unless our 210Pb-derived sedimentation rates are incorrectly high. However, they are in good agreement with previous 210Pb and varve chronologies in Saanich Inlet, and also give reasonable dates for times when 239 + 240Pu and SNAP-9A supplied 238Pu first appear in the sediments. We conclude they properly date the maximum in sedimentary 239 + 240Pu activity at 1970–1973, and seek explanations for the 7–10yr time lag after peak fallout.239 + 240Pu inventories in one core from the eastern basin of the Cariaco Trench and in two cores from Golfo Dulce. an anoxic basin off the Pacific coast of Costa Rica, are also in reasonable agreement with fallout delivery to these latitudes when excess 210Pb inventories and fluxes are used to verify recovery of at least a major fraction of the most recently deposited sediments.  相似文献   

5.
The isotopic compositions of S (δ34S) and C (δ13C) were determined for the coal utilized by a power plant and for the fly ash produced as a by-product of the coal combustion in a 220-MW utility boiler. The coal samples analyzed represent different lithologies within a single mine, the coal supplied to the power plant, the pulverized feed coal, and the coal rejected by the pulverizer. The ash was collected at various stages of the ash-collection system in the plant. There is a notable enrichment in 34S from the base to the top of the coal seam in the mine, with much of the variation due to an upwards enrichment in the δ34S values of the pyrite. Variations in δ34S and in the amount of pyritic S in the coal delivered to the plant show that there was a change of source of coal supplied to the plant, between week one and week two of monitoring, supporting a previous study based on metal and sulfide geochemistry for the same plant. The fly ash has a more enriched δ34S than the pulverized coal and, in general, the δ34S is more enriched in fly ashes collected at cooler points in the ash-collection system. This pattern of δ34S suggests an increased isotopic fractionation due to temperature, with the fly ash becoming progressively depleted in 34S and the flue gas S-containing components becoming progressively enriched in 34S with increasing temperatures. Substantially less variation is seen in the C isotopes compared to S isotopes. There is little vertical variation in δ13C in the coal bed, with δ13C becoming slightly heavier towards the top of the coal seam. An 83–93% loss of solid phase C occurs during coal combustion in the transition from coal to ash owing to loss of CO2. Despite the significant difference in total C content only a small enrichment of 0.44–0.67‰ in 13C in the ash relative to the coal is observed, demonstrating that redistribution of C isotopes in the boiler and convective passes prior to the arrival of the fly ash in the ash-collections system is minor.  相似文献   

6.
Major and trace elements in groundwater from basaltic aquifers in pristine conditions were investigated in a volcanic island to evaluate sources, sinks, and mobility of elements over a wide range of mineralization conditions with total dissolved solids from 50 mg/L to 3400 mg/L. Groundwater was highly undersaturated with respect to primary silicate minerals, indicating that dissolution of basaltic rocks may continue under conditions with precipitation of calcite and secondary silicates. Evolution of B/Cl ratio in groundwater from marine aerosols to basaltic rocks showed that the ratio could be used as a conservative tracer for interactions between water and basaltic rocks. Relative mobility (RM) of elements calculated using the concentrations of elements in the local basaltic rocks and those in groundwater showed that mobility decreased in the order of B > Rb > Na > K > Mg > Ca > Mo > V > Si > Sr > Sc > P > U > Zn > Pb > Cr > Cu > Ba > Ni > Ti > (Mn, Al, Fe, Co, Th) indicating that oxyanion-forming elements and alkali metals had the highest mobility. Compared to average RM, V had decreased mobility, and Fe and Mn had increased mobility in anoxic groundwater while V, Mo, and U had higher mobility in oxic-alkaline water. The sources of V, Cr, Cu, and Zn in rocks were estimated using the partition coefficients between minerals and basaltic melt, and the disparity between sources and mobility indicated that sinks are more important for controlling the concentrations of these elements in groundwater than the contents in the rocks. Principal component analysis (PCA) of hydrogeochemical parameters in groundwater produced three principal components (PC) which represent dissolution of basaltic rocks without significant attenuation of released solutes, higher degree of water–rock interactions resulting in oxic-alkaline conditions, and attenuation of Zn and Cu in higher pH, respectively. Spatial distribution of PCs revealed that groundwater with elevated concentrations of mobile elements was concentrated in the southwestern area and that concentrations of V and Cr were more scattered, which is likely to be controlled by pH and redox states of groundwater as well as degree of water–rock interactions.  相似文献   

7.
分析了2014~2018年北方5个典型中小盆地城市(兰州、银川、临汾、太原、南阳)PM10与PM2.5的浓度变化特征和大致来源类型。除2018年银川PM2.5浓度外,各市PM10和PM2.5年均浓度均超标;兰州、银川和南阳PM10与PM2.5呈逐年下降趋势,南阳下降最明显;临汾PM10与PM2.5呈逐年上升趋势;太原PM10与PM2.5稳定维持在一个高浓度状态。5个城市颗粒物浓度的季节变化特征一致:冬春高、夏秋低。对PM2.5/PM10值而言,冬季和夏季该比值较高,分别受取暖和降水的影响;春季和秋季该比值较低,分别受沙尘和秸秆焚烧及高强度建筑施工的影响。5市PM2.5和PM10浓度具有良好的线性关系,细颗粒占比大小顺序为临汾>南阳>太原>银川>兰州。  相似文献   

8.
A survey is made of various factors influencing the 13C12C ratio of the organic component in lake sediments, focusing on the behaviour at the change from glacial to post-glacial environmental conditions.Increase in the 13C content of the organic sediment is caused by increase in temperature and the corresponding decrease of the supply of molecular CO2 in the water of the lakes. An increase in the rate of organic production in the lakes may also, perhaps, cause a corresponding 13C increase. An increase of the fermentation of organic mud in the lakes may also have an effect in the same direction.Decrease in the 13C content of the organic sediment is caused by the change of the relative amounts of production of plankton and submersed macrophytes in the lakes from mainly submersed macrophytes to mainly plankton. A decrease towards almost complete absence of bicarbonate and CO2 originating from carbonate rocks will also lead to a 13C decrease in the organic sediments. The same effect has the change of the terrestrial vegetation cover from almost complete absence to complete cover. A possible decrease of the 13C content in the atmospheric CO2 has an effect in the same direction.  相似文献   

9.
Earthquakes in Switzerland and surrounding regions during 2004   总被引：1，自引：0，他引：1  
This report of the Swiss Seismological Service summarizes the seismic activity in Switzerland and surrounding regions during 2004. During this period, 677 earthquakes and 96 quarry blasts were detected and located in the region under consideration. With 22 events with ML≥2.5, the seismic activity in the year 2004 was close to the average over the last 30 years. As in previous years, most of the activity was concentrated in the Valais and in Graubünden. In addition, several moderate earthquakes occurred in the lower crust below the northern Alpine foreland. Unusual was that five earthquakes were sufficiently strong to cause ground shaking of intensity IV over large portions of the territory. Two were located in Switzerland (Liestal, ML 3.8, and Brugg, ML 4.0). The epicenters of the other three strong events were located outside Switzerland (Besan?on in the French Jura, ML 4.8, Waldkirch in southern Germany, ML 5.1, and Lago di Garda in northern Italy, ML 5.3).  相似文献   

10.
The partitioning of samarium and thulium between garnets and melts in the systems Mg3Al2-Si3O12-H2O and Ca3Al2Si3O12-H2O has been studied as a function of REE concentration in the garnets at 30 kbar pressure. Synthesis experiments of variable time under constant P, T conditions indicate that garnet initially crystallizes rapidly to produce apparent values of D Sm (D Sm=concentration of Sm in garnet/concentration of Sm in liquid) which are too large in the case of pyrope and too small in the case of grossular. As the experiment proceeds, Sm diffuses out of or into the garnet and the equilibrium value of D Sm is approached. Approximate values of diffusion coefficients for Sm in pyrope garnet obtained by this method are 6 × 10–13 cm2 s–1 at 1,300 ° C and 2 × 10–12 cm2 s–1 at 1,500 ° C, and for grossular, 8.3 × 10–12 cm2 s–1 at 1,200 ° C and 4.6 × 10–11 cm2 s–1 at 1,300 ° C. The equilibrium values of D Sm have been reversed by experiments with Sm-free pyrope and Sm-bearing glass, and with Sm-bearing grossular and Sm-free glass.Between 12 ppm and 1,000 ppm Sm in pyrope at 1,300 ° C and between 80 ppm and >2 wt.% Tm in pyrope at 1,500 ° C, partition coefficients are constant and independent of REE concentration. Above 100 ppm of Sm in garnet at 1,500 ° C, partition coefficients are independent of Sm concentration. At lower concentrations, however, D Sm is dependent upon the Sm content of the garnet. The two regions may be interpreted in terms of charge-balanced substitution of Sm3Al5O12 in the garnet at high Sm concentrations and defect equilibria involving cation vacancies at low concentrations. At very low REE concentrations (< 1 ppm Tm in grossular at 1,300 ° C) DREE garnet/liquid again becomes constant with an apparent Henry's Law value greater than that at high concentrations. This may be interpreted in terms of a large abundance of cation vacancies relative to the number of REE ions.The importance of defects in the low concentration region has been confirmed by adding other REE (at 80 ppm level) to the system Mg3Al2Si3O12-H2O at low Sm concentrations. These change D Sm in the defect region, demonstrating their role in the production of vacancies.Experiments on a natural pyropic garnet indicate that defect equilibria are of importance to REE partitioning within the concentration ranges found in nature.  相似文献   

11.
Unaltered metasediments of the Mary Kathleen Fold Belt are composed predominantly of layered amphibolite-facies scapolitic calc-silicate rocks in which minimal infiltration of externally derived fluids occurred during regional metamorphism. There were substantial differences in volatile activities between different layers in the layered sequences, in particular: a CO2/a H 2 O inferred from reaction progress estimates and analysis of biotite-clinopyroxene-fluid phase relations; a NaCl/a H 2 O inferred from scapolite compositions; and a HCl/a H 2 O inferred from biotite compositions. In one outcrop in which a clinopyroxene-producing reaction dominated, differences in approximate X CO 2of up to 0.25 occurred between several samples collected over 50 metres. Variations in a H 2 O/a HCl of up to one order of magnitude are inferred at 1 to 50 m scales from biotite-Cl contents, and variations in NaCl contents of scapolite from 0.0 to up to 0.6 Cl atoms in the Cl–CO3–SO4 site reflect a large variation of a NaCl in the coexisting fluid at similar scales. Most calcsilicate layers internally buffered fluid compositions in the H2O–CO2–NaCl–HCl system. Local occurrences of NaCl-rich scapolite suggest that some layers may have been in equilibrium with halite during early prograde metamorphism. At peak metamorphic temperatures, disolution of halite was complete but layers containing high-NaCl scapolite continued to buffer fluid at high values of a NaCl. Fluid immiscibility does not appear to have affected the progress of the devolatilization reactions. Although fluid was predominantly internally buffered, moderate quantities of fluid were released by prograde mineral reactions in many layers, up to 30 cm3 fluid per 100 cm3 rock. Numerous episodes of fluid escape were required, probably via microfractures, such that the released fluid did not obviously influence reaction progress in the layers through which it passed. The anomaly of beautifully preserved internal buffering signatures and the requirement for produced fluid locally to pass across layers in a deforming rock sequence suggest that the escaping fluid did not leave any readily observable tracks. This is explained by rapid rates of fracture propogation and fluid migration therein. This internally buffered system contrasts strongly with adjacent calc-silicate rocks that show evidence for infiltration of externally derived fluids at high fluid/rock ratios, and highlights the broad range of fluid behaviour that can be expected in deforming, heterogeneous rock sequences.  相似文献   

12.
Rapid temperature change causes fractionation of isotopic gaseous species in air in firn (snow) by thermal diffusion, producing a signal that is preserved in trapped air bubbles as the snow forms ice. Using a model of heat penetration and gas diffusion in the firn, as well as the values of appropriate thermal diffusion constants, it is possible to reconstruct the magnitude of a particular paleoclimate change. Isotopic nitrogen in air serves as a convenient tracer for such paleoreconstruction, because the ratio 29N2/28N2 has stayed extremely constant in the atmosphere for ≥106 years. However, prior to this work no data were available for thermal diffusion of 29N2/28N2 in air, but only in pure N2. We devised a laboratory experiment allowing fractionation of gases by thermal diffusion in a small, tightly controlled temperature difference. A mass spectrometer was employed in measuring the resulting fractionations yielding measurement precision greater than was attainable by earlier thermal diffusion investigators.Our laboratory experiments indicate that the value of the thermal diffusion sensitivity (Ω) for 29N2/28N2 in air is +(14.7 ± 0.5) × 10−3 per mil/°C when the average temperature is -30.0°C. The corresponding value for 29N2/28N2 in pure N2 that we find is +(15.3 ± 0.4) × 10−3 per mil/°C at -30.6°C, in agreement with the previously available literature data within their large range of uncertainty. We find that an empirical equation, Ω = (8.656/TK − 1232/T K2) ± 3% per mil/°C, describes the slight variation of the sensitivity values for 29N2/28N2 in air with temperature in the range of -60 to 0°C. A separate set of experiments also described in this paper rules out adsorption as a candidate for producing additional temperature change-driven fractionation of 29N2/28N2 in the firn air. The combined newly obtained data constitute a calibration of the fossil-air paleothermometer with respect to isotopic nitrogen and will serve to improve the estimates of the magnitudes of past abrupt climate changes recorded in ice cores.  相似文献   

13.
The discovery of natural 210Po enrichment at levels exceeding 500 mBq/L in numerous domestic wells in northern Nevada, USA, led to a geochemical investigation of the processes responsible for its mobilization. 210Po activities in 63 domestic and public-supply wells ranged from below 1 mBq/L to 6590 ± 590 mBq/L, among the highest reported levels in the USA. There is little spatial or depth variability in 210Pb activity in study-area sediments and mobilization of a few percent of the 210Po in the sediments would account for all of the 210Po in water. Stable-isotope measurements indicate SO4 reduction has occurred in all 210Po contaminated wells. Sulfide species are not accumulating in the groundwater in much of Lahontan Valley, probably because of S cycling involving microbial SO4 reduction, abiotic oxidation of H2S to S0 by Mn(IV), followed by microbial disproportionation of S0 to H2S and SO4. The high pH, Ca depletion, MnCO3 saturation, and presence of S0 in Lahontan Valley groundwater may be consequences of the anaerobic S cycling. Consistent with data from naturally-enriched wells in Florida, 210Po activities begin to decrease when aqueous sulfide species begin to accumulate. This may be due to formation and precipitation of PoS, however, Eh-pH diagrams suggest PoS would not be stable in study-area groundwater. An alternative explanation for the study area is that H2S accumulation begins when anaerobic S cycling stops because Mn oxides are depleted and their reduction is no longer releasing 210Po. Common features of 210Po-enriched groundwater were identified by comparing the radiological and geochemical data from Nevada with data from naturally-enriched wells in Finland, and Florida and Maryland in the USA. Values of pH ranged from <5 in Florida wells to >9 in Nevada wells, indicating that pH is not critical in determining whether 210Po is present. Where U is present in the sediments, the data suggest 210Po levels may be elevated in aquifers with (1) SO4-reducing waters with low H2S concentrations, or (2) anoxic or oxic waters with extremely high Rn activities, particularly if the water is turbid.  相似文献   

14.
Lipid biomarkers and 13C fractionation patterns were used to understand the dynamics of carbon cycling during microbial metabolisms in different environments of travertine precipitation (called facies) at Spring AT-1 on Angel Terrace in the Mammoth Hot Springs complex of Yellowstone National Park, USA. Microbial mats that encrust travertine deposits were collected for analyses of lipid biomarkers and carbon isotopes along the continuous drainage outflow system of Spring AT-1. The spring water exhibits a continuous temperature drop from 71°C in the vent at top to 24°C in the distal slope at bottom. Phospholipid fatty acids (PLFA) and glycolipid fatty acids (GLFA) exhibit distinctly different compositions in each of the facies, which are consistent with partitioning of the bacterial 16S rRNA gene sequences in the Spring AT-1 travertine facies (Fouke et al., 2003).The δ13C composition of total biomass within the microbial mats decreases from −16.1‰ in the vent to −23.5‰ in the distal slope. However, lower values occur in the pond (−26.0‰) and the proximal slope (−28.0‰) between the vent and the distal slope. Isotopic compositions of PLFA and GLFA have variations similar to those of total biomass. The average δ13C values of PLFA are −12.4 ± 5.2‰ (n = 10 individual fatty acids, same below) in the vent, −33.0 ± 3.1‰ (n = 11) in the pond, −33.7 ± 3.8‰ (n = 16) in the proximal slope, and −22.4 ± 3.4‰ (n = 10) in the distal slope; the average δ13C values of GLFA are −19.6 ± 3.0‰ (n = 3) in the vent, −30.4 ± 4.7‰ (n = 8) in the pond, −36.9 ± 2.8‰ (n = 12) in the proximal slope, and −27.9 ± 3.1‰ (n = 13) in the distal slope. In particular, fatty acids in the vent are enriched in 13C relative to the total biomass, which is consistent with the notion that the biosynthetic pathways of the extant microbial community in the vent may be dominated by Aquificales using the reversed tricarboxylic acid cycle. Fractionations between fatty acids and total biomass in the pond, the proximal slope and the distal slope suggest the involvement of other biosynthetic pathways for CO2 fixation by extant microbial populations. The results indicate that lipid biomarkers provide valuable information on the changing diversity and activity of microbial communities in different depositional environments. Carbon-isotope fractionations, on the other hand, can provide insight into the operating biosynthetic pathways associated with different organisms in the changing environment. This integrated approach may serve as a powerful tool for identifying functional metabolism within a community and identify shifts in microbial community structure in modern hot-spring systems.  相似文献   

15.
High Arsenic (As) concentrations have been reported in superficial water in the Yamuna flood plains (YFP), Delhi, which is being extensively used for agriculture. The concentration of As in some common vegetables such as Solanum lycopersicum (tomato), Abelmoschus esculentus (lady’s finger), Solanum melongena (brinjal), Lagenaria siceraria (bottle gourd), Raphanus sativus (radish), Zea mays (corn), and Luffa acutangula (ridge gourd) has been studied in this work. The range of As concentrations (dry weight) varies from 0.6 to 2.52 mg/kg with the highest accumulation of 2.52 mg/kg in radish followed by tomato (2.36 mg/kg). The order of As concentration in the decreasing order is R. sativus > S. lycopersicum > Z. mays > L. acutangula > L. siceraria > S. melongena > A. esculentus. Thus, As accumulation is the highest in roots and the lowest in least juicy fruits. The daily dietary intake of As through the consumption of various vegetables was also calculated. Though the mean As concentration was the highest in radish (2.52 mg/kg) but the highest amount of As is being consumed through tomato (0.383 mg/day), which is nearly three times the World Health Organization’s provisional maximum tolerable daily intake limit of 0.126 mg/day for a 60 kg person. High concentration of As in vegetables grown in YFP, Delhi is being reported here. This high contamination is primarily due to the presence of As in irrigation water having its source from coal-based thermal power plants in the vicinity of the area. If not checked properly, it will pose a serious health risk to people living in these densely populated areas surrounding YFP.  相似文献   

16.
The Daliao river system in China has been seriously affected by long-term intensive industrial, urban and agricultural activities. The objectives of this study were to determine the total phosphorus (TP) content and forms of phosphate in the sediments and investigate geochemical relationships between P forms and sediment mineral phases. Twenty-seven samples of surface sediments were collected and analyzed for P and major elements. Chemical forms of phosphate in the sediments were measured by sequential selective extraction method. Results indicate that TP in the sediments of the Daliao river system averaged 703 mg kg−1, in the range from 206 to 1,342 mg kg−1. The sediments in the tributaries and near cities contained high TP, due to discharge of municipal and industrial effluents. The distribution of phosphate in the various mineral phases followed the order: Ca-P > RES-P > RS-P > Fe-P > Al-P > S/L-P for the Hun river and Taizi river, and Ca-P > Fe-P > RES-P > RS-P > Al-P > S/L-P for the Daliao river. Fe and Ca contents in the sediments were positively correlated to Fe associated P (Fe-P and RS-P) and Ca-P, respectively. In addition, sediment organic matter, Fe and Ca contents were positively correlated to TP in the sediments. However, Al content was not correlated to Al-P or TP in the sediments. Generally, the sediments contaminated by effluents and in tidal zone contained more bioavailable P. Possible release of P from these sediments to overlying water might pose potential risk on estuarine eutrophication.  相似文献   

17.
Phase equilibria data in the systems SiO2-P2O5, P2O5-MxOy, and P2O5-MxOy-SiO2 are employed in conjunction with Chromatographic and spectral data to investigate the role of P2O5 in silicate melts. Such data indicate that the behavior of P2O5 is complex. P2O5 depolymerizes pure SiO2 melts by entering the network as a four-fold coordinated cation, but polymerizes melts in which an additional metal cation other than silicon is present. The effect of this polymerization is apparent in the widening of the granite-ferrobasalt two-liquid solvus. In this complex system P2O5 acts to increase phase separation by further enrichment of the high charge density cations Ti, Fe, Mg, Mn, Ca, in the ferrobasaltic liquid. P2O5 also produces an increase in the ferrobasalt-granite REE liquid distribution coefficients. These distribution coefficients are close to 4 in P2O5-free melts, but close to 15 in P2O5-bearing melts.The dual behavior of P2O5 is explained in a model which requires complexing of phosphate anions (analogous to silicate anions) and metal cations in the melt. This interaction destroys Si-O-M-O-Si bonds polymerizing the melt. The higher concentration of Si-O-M-O-Si bond complexes in immiscible ferrobasaltic liquids relative to their conjugate immiscible granite liquids explains the partitioning of P2O5 into the ferrobasaltic liquid.  相似文献   

18.
In this work, the total and each fraction concentration of toxic metals (Pb, Zn, Cu and Cd) in soils as well as in plants from a typical metallurgical industrial area in southwest of China were determined. The obtained experimental results demonstrated that the total toxic metal content in contaminated soils was in the order of Zn > Pb > Cu > Cd. Modified microwave-assisted extraction showed that the distributions of each fraction of toxic metals in soils were different and some soil properties may play a role in the fraction distributions. The content of Cu, Zn, Cd and Pb in different vegetables ranged from 9.82 ± 1.02 to 39.3 ± 1.13 mg kg?1, 1,321 ± 10.50 to 3,153 ± 11.30 mg kg?1, 4.47 ± 0.21 to 18.9 ± 0.37 mg kg?1 and 28 ± 1.2 to 102 ± 1.5 mg kg?1, respectively. And the accumulation of toxic metals in plants was in the order of Cd > Zn > Cu > Pb. The bioconcentration factor (BCF) values of Cd, Zn, Cu and Pb in the different tissues of plants were in the range of 0.03–0.43, 0.027–0.35, 0.014–0.12 and 0.004–0.051, respectively. The distribution of each toxic metal in plants indicated that the ability for plants to accumulate toxic metals in different tissues followed the sequence of leaf > stem.  相似文献   

19.
It is shown the possibility to determine the coordination of paramagnetic ions in disordered solid structures, e.g., in barium borate glasses. For this purpose the electron paramagnetic resonance (EPR) method was used to study α-and β-BaB2O4 crystals and glasses of 45·BaO × 55·B2O3 and 40·BaO × 60·B2O3 (mol%) composition activated by Ag+ and Pb2+ ions. After the samples were exposed to X-rays at 77 K, different EPR centers were observed in them. In α-and β-BaB2O4 crystals and glasses the EPR centers Ag2+, Ag0, Pb+, Pb3+, and hole centers of O− type were studied. The EPR parameters of these centers and their arrangement in crystal structure were determined. It is shown that Pb3+ ions in β-BaB2O4 crystals occupy Ba2+ position in an irregular polyhedron from the eight oxygen, whereas in α-BaB2O4 crystals they occupy Bа2 position in a sixfold coordination. Pb+ ions in α-BaB2O4 crystals occupy Bа1 position in a ninefold coordination from oxygen. In barium borate glasses, Pb3+ ions were studied in coordination polyhedron from six oxygen atoms and in a polyhedron from nine to ten oxygen atoms. It is assumed that the established difference in the structural position of Pb3+ ions in glasses is due to their previous incorporation in associative cation–anion complexes (AC) and “free” structure-forming cations (FC). Computer simulations have been performed to analyze the stability of specific associative complexes and to compare their bond lengths with experimental data.  相似文献   

20.
Weathering fluxes of arsenic from a small catchment in Slovak Republic   总被引：1，自引：1，他引：0  
Inputs of As to a small catchment due to chemical weathering of bedrock, mechanical weathering of bedrock, and atmospheric precipitation were 71.53, 23.98 and 0.02 g ha−1 year−1, respectively. The output fluxes of As due to mechanical erosion of soil, biological uptake, stream discharge, and groundwater flow were 6.32, 4.77, 0.37 and 0.02 g ha−1 year−1, respectively. The results indicate that arsenic accumulates in soil and regolith with a very high rate. This is attributed to the selective weathering and erosion with respect to arsenic and fixation of arsenic in the secondary solids produced by weathering. The output fluxes of As in stream and groundwater in Vydrica catchment in Slovak Republic (0.39 g ha−1 year−1) based on muscovite–biotite granites and granodiorites were much lower compared to catchments in a gold district in the Czech Republic. These results may be ascribed to the low levels of arsenic pollution measured in Vydrica catchment. The arsenic fluxes were estimated by calculation of mechanical and chemical weathering rates of the bedrocks in Vydrica catchment from mass balance data on sodium and silica. The justification of the steady state of Na and Si is that neither of the elements is appreciably accumulated in plants and in exchangeable pool of ions in soil.  相似文献   

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