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1.
Heavy metals are governed by parent material of soils and influenced by the soil physicochemical properties and soil and crop management practices. This paper evaluates total heavy metal concentrations in rainfed soils under diverse management practices of tropical India. Vertisols (clayey soils with high shrink/swell capacity) had the highest concentrations of heavy metals. However, chromium (Cr) content was above the threshold value in Aridisol [calcium carbonate (CaCO3)]-containing soils of the arid environments with subsurface horizon development. Concentration increased at lower depths (>30 cm). Basaltic soils showed higher concentrations of nickel (Ni), copper (Cu) and manganese (Mn). Cadmium (Cd), cobalt (Co), Cu and Mn concentrations were higher in soils cultivated to cotton, whereas Cr concentration was above the threshold level of 110 mg kg?1 in food crop cultivated soils. As the specific soil surface is closely related to clay content and clay type, soil’s ability to retain heavy metals is more closely tied to the specific surface than to the soil cation exchange capacity. Higher positive correlations were found between heavy metal concentrations and clay content [Cd(r = 0.85; p ≤ 0.01); Co (r = 0.88; p ≤ 0.05); Ni (r = 0.87; p ≤ 0.01); Co (r = 0.81; p ≤ 0.05); Zn (r = 0.49; p ≤ 0.01); Cr (r = 0.80; p ≤ 0.05); Mn (r = 0.79; p ≤ 0.01)]. The amounts of nitrogen–phosphorus–potassium applied showed a positive correlation with Co and Ni (r = 0.62; p ≤ 0.05). As several soils used for growing food crops are high in Ni, Cr and Mn, the flow of these metals in soil–plant–livestock/human chain needs further attention.  相似文献   

2.
《Applied Geochemistry》2004,19(10):1553-1565
Recent research has shown that phytoextraction approaches often require soil amendments, such as the application of EDTA, to increase the bioavailability of heavy metals in soils. However, EDTA and EDTA–heavy metal complexes can be toxic to plants and soil microorganisms and may leach into groundwater, causing further environmental pollution. In the present study, vetiver grass (Vetiveria zizanioides) was studied for its potential use in the phytoremediation of soils contaminated with heavy metals. In the pot experiment, the uptake and transport of Pb by vetiver from Pb-contaminated soils under EDTA application was investigated. The results showed that vetiver had the capacity to tolerate high Pb concentrations in soils. With the application of EDTA, the translocation ratio of Pb from vetiver roots to shoots was significantly increased. On the 14th day after 5.0 mmol EDTA kg−1 of soil application, the shoot Pb concentration reached 42, 160, 243 mg kg−1 DW and the root Pb concentrations were 266, 951, and 2280 mg kg−1 DW in the 500, 2500 and 5000 mg Pb kg−1 soils, respectively. In the short soil leaching column (9.0-cm diameter, 20-cm height) experiment, about 3.7%, 15.6%, 14.3% and 22.2% of the soil Pb, Cu, Zn and Cd were leached from the artificially contaminated soil profile after 5.0 mmol EDTA kg−1 of soil application and nearly 126 mm of rainfall irrigation. In the long soil leaching experiment, soil columns (9.0-cm diameter, 60-cm height) were packed with uncontaminated soils (mimicking the subsoil under contaminated upper layers) and planted with vetiver. Heavy metal leachate from the short column experiment was applied to the surface of the long soil column, the artificial rainwater was percolated, and the final leachate was collected at the bottom of the soil columns. The results showed that soil matrix with planted vetiver, could re-adsorb 98%, 54%, 41%, and 88% of the initially applied Pb, Cu, Zn, and Cd, respectively, which may reduce the risk of heavy metals flowing downwards and entering the groundwater.  相似文献   

3.
A pot experiment was conducted to monitor the dynamic response of photosynthesis of Amorpha fruticosa seedlings to different concentrations of petroleum-contaminated soils from April to September. The results showed that the photosynthetic rates, stomatal conductance and transpiration rate of seedlings significantly decreased in 5–20 g kg?1 petroleum-contaminated soil during the three given sampling period of July 31 (early), August 30 (mid-term) and September 29 (late). However, the intercellular CO2 concentration significantly increased in 10 g kg?1 contaminated soil, while declined in 20 g kg?1 contaminated soil during the early sampling period as well as in 20 g kg?1 contaminated soil during the late sampling period. The leaf relative water content of seedlings significantly increased in 20 g kg?1 contaminated soil during the early sampling period, while it dropped dramatically in 15–20 g kg?1 contaminated soil during the late sampling period. The contents of chlorophyll a, chlorophyll b and the total chlorophyll of seedlings showed a sharp decline during the three sampling periods in contaminated soil. Comprehensively, considering the negative effects of petroleum on the photosynthesis, growth performance and remediation effect on petroleum of A. fruticosa seedlings, this plant was tolerant of petroleum-contaminated soil and was potentially useful for the phytoremediation of petroleum-contaminated sites in northern Shaanxi, China.  相似文献   

4.
The purpose of this study was to investigate the effect of phytoremediation on soils contaminated with heavy crude oil using plants infected by mycorrhizal fungi. Five plant species, Vetiveria zizanioides, Bidens pilosa, Chloris barbata, Eleusine indica, and Imperata cylindrica, infected with the species of mycorrhizal fungi Glomus mosseae, were selected for this study. The degradation of total petroleum hydrocarbons in soils and several physiological parameters of plants such as shoot length and biomass were analyzed. Out of the 5 plant species tested, only V. zizanioides, B. pilosa, and E. indica could take up the G. mosseae. Out of these three, V. zizanioides showed the greatest growth (biomass) in soils with 100,000 mg kg?1 total petroleum hydrocarbons. In addition, B. pilosa infected with G. mosseae was found to be able to increase degradation by 9 % under an initial total petroleum hydrocarbons concentration of 30,000 mg kg?1 in soils after 64 days. We conclude that plants infected with mycorrhizal fungi can enhance the phytoremediation efficiency of soils contaminated with high concentrations of heavy oil.  相似文献   

5.
This study investigated the effect of cations and anions on the sorption and desorption of iron (Fe) and manganese (Mn) in six surface calcareous soil samples from Western Iran. Six 10 mM electrolyte background solutions were used in the study, i.e., KCl, KNO3, KH2PO4, Ca(NO3)2, NaNO3, and NH4NO3. NH4NO3 and NaNO3 increased the soil retention of Fe and Mn, whereas Ca(NO3)2 decreased the soil retention of Fe and Mn. Iron and Mn sorption was decreased by NO3 ? compared with H2PO4 ? or Cl?. The Freundlich equation adequately described Fe and Mn adsorption, with all background electrolytes. The Freundlich distribution coefficient (K F) decreased in the order H2PO4 ? > Cl? > NO3 ? for Mn and H2PO4 ? > NO3 ? > Cl? for Fe. The highest sorption reversibility was for Fe and Mn in competition with a Ca2+ background, indicating the high mobility of these two cations. A MINTEQ speciation solubility model showed that Fe and Mn speciation was considerably affected by the electrolyte background used. Saturation indices indicated that all ion background solutions were saturated with respect to siderite and vivianite at low and high Fe concentrations. All ion background solutions were saturated with respect to MnCO3(am), MnHPO4, and rhodochrosite at low and high Mn concentrations. The hysteresis indices (HI) obtained for the different ion backgrounds were regressed on soil properties indicating that silt, clay, sand, and electrical conductivity (EC) were the most important soil properties influencing Fe adsorption, while cation exchange capacity (CEC), organic matter (OM), and Mn-DTPA affected Mn adsorption in these soils.  相似文献   

6.
The chemical analysis of plants and soils is a frequently used approach in understanding a serpentine ecosystem. Studies on vegetation growth in serpentine soils focused on various plant species for remediation purposes of soil contamination with heavy metals, emphasizing their role in the metal extraction or stabilization in the soil. The aims of this study were to measure the concentrations of Cr, Mn, and Ni in the soils and plants and to elucidate the phytoremediation potential of the studied plants. This study was performed at an abandoned site of serpentine mining in eastern Taiwan. Seven plant species were collected for analysis of Cr, Mn, and Ni, including Crotalaria micans, Miscanthus floridulus, Leucaena leucocephala, Bidens pilosa, Pueraria lobata, Melilotus indicus, and Conyza canadensis. The Cr and Ni concentrations in all studied plants were higher than those in general plants. In all species, the mean concentrations of Cr, Mn, and Ni in the shoots were lower than those in the root. None of the collected specimens exhibited hyperaccumulation of Cr, Mn, and Ni. All studied species may be used to remediate contaminated soils through phytostabilization of Cr and Mn, whereas M. floridulus and M. indicus are appropriate plants for phytostabilization of Ni. However, C. micans, L. leucocephala, B. pilosa, P. lobata, and C. canadensis have the potential to remove Ni from contaminated soils for the purpose of phytoextraction.  相似文献   

7.
Plant and soil samples were collected from one uncontaminated and four contaminated sites (in the Dashkasan mining area western Iran). Total and water-soluble arsenic in the soil ranged from 7 to 795 and from 0.007 to 2.32 mg/kg, respectively. The highest arsenic concentration in soil was found at the ore dressing area (up to 1,180 mg/kg) and lowest at an uncontaminated area (up to 11 mg/kg). A total of 49 plant species belonging to 15 families were collected from four sampling sites. A significant positive correlation was detected between the concentrations of arsenic in plant dry matter and those in soils. The highest arsenic concentrations were found in Hyoscyamus kurdicus Bornm. (up to 205 mg/kg) and Helichrysum oligocephalum DC. (up to 162 mg/kg). These two accumulator species could have potential for soil clean-up by phytoextraction. The data have been compared with those for the Zarshuran mining area (north-western Iran) obtained in a former study.  相似文献   

8.
Dehoo manganese deposit is located 52 km to the south of Zahedan in Sistan and Baluchestan Province, southeastern Iran. This deposit that lies in the central part of the Iranian Flysch Zone is lenticular in shape and lies above the micritic limestone-radiolarite cherts of the upper Cretaceous ophiolite unit. It is hosted within the reddish to brown radiolarite cherts and in places interlinks with them, so that the radiolarite chert packages play a key role for Mn mineralization in the region. Investigated ore-paragenetic successions and the geochemical characteristics of the Dehoo deposit were studied by means of major oxide, trace, and rare earth element (REE) contents that provide information as to the mineral origin. Strong positive correlations were found between major oxides and trace elements (Al2O3-TiO2, r = 0.95; TiO2-MgO, r = 0.94; Fe2O3-Al2O3, r = 0.90; MgO-Al2O3, r = 0.84; MgO-Fe2O3, r = 0.88; Fe2O3-TiO2, r = 0.91; Fe2O3-K2O, r = 0.74; Al2O3-K2O, r = 0.69; Al2O3-V, r = 0.72; TiO2-V, r = 0.73, and MgO-V, r = 0.69) that testify to the contribution of mafic terrigenous detrital material to the deposit. Chondrite-normalized REE patterns of all ore samples are characterized by negative Ce (0.06–0.15, average 0.10) and slightly positive Eu (0.29–0.45, average 0.36) anomalies. Based on ratios of Mn/Fe (average 56.23), Co/Ni (average 0.33), Co/Zn (average 0.38), U/Th (average 3.40), La/Ce (average 1.45), Lan/Ndn (average 2.16), Dyn/Ybn (average 0.33), and light REE/heavy REE (average 8.40; LREE > HREE), as well as Ba (average 920 ppm) and total REE contents (average 6.96 ppm) negative Ce and positive Eu anomalies, Dehoo could be considered a predominantly submarine hydrothermal Mn deposit complemented by terrigenous detrital mafic material.  相似文献   

9.
Minerals constitute a primary ecosystem control on organic C decomposition in soils, and therefore on greenhouse gas fluxes to the atmosphere. Secondary minerals, in particular, Fe and Al (oxyhydr)oxides—collectively referred to as “oxides” hereafter—are prominent protectors of organic C against microbial decomposition through sorption and complexation reactions. However, the impacts of Mn oxides on organic C retention and lability in soils are poorly understood. Here we show that hydrous Mn oxide (HMO), a poorly crystalline δ-MnO2, has a greater maximum sorption capacity for dissolved organic matter (DOM) derived from a deciduous forest composite Oi, Oe, and Oa horizon leachate (“O horizon leachate” hereafter) than does goethite under acidic (pH 5) conditions. Nonetheless, goethite has a stronger sorption capacity for DOM at low initial C:(Mn or Fe) molar ratios compared to HMO, probably due to ligand exchange with carboxylate groups as revealed by attenuated total reflectance-Fourier transform infrared spectroscopy. X-ray photoelectron spectroscopy and scanning transmission X-ray microscopy–near-edge X-ray absorption fine structure spectroscopy coupled with Mn mass balance calculations reveal that DOM sorption onto HMO induces partial Mn reductive dissolution and Mn reduction of the residual HMO. X-ray photoelectron spectroscopy further shows increasing Mn(II) concentrations are correlated with increasing oxidized C (C=O) content (r = 0.78, P < 0.0006) on the DOM–HMO complexes. We posit that DOM is the more probable reductant of HMO, as Mn(II)-induced HMO dissolution does not alter the Mn speciation of the residual HMO at pH 5. At a lower C loading (2 × 102 μg C m?2), DOM desorption—assessed by 0.1 M NaH2PO4 extraction—is lower for HMO than for goethite, whereas the extent of desorption is the same at a higher C loading (4 × 102 μg C m?2). No significant differences are observed in the impacts of HMO and goethite on the biodegradability of the DOM remaining in solution after DOM sorption reaches steady state. Overall, HMO shows a relatively strong capacity to sorb DOM and resist phosphate-induced desorption, but DOM–HMO complexes may be more vulnerable to reductive dissolution than DOM–goethite complexes.  相似文献   

10.
Greenhouse tests were conducted to study the effect of chelates on the phytoextraction of cadmium and lead, and the rhizodegradation of used engine oil present as a mixed contaminant in a sandy soil. Indian mustard plants were grown in test pot soil for 30 days and chelates ethylenediamine tetraacetic acid (EDTA) and ethylenediaminedisuccinic acid (EDDS) were individually applied to the test soil. The soil was spiked earlier with 50 mg kg?1 of CdCl2, 500 mg kg?1 of PbCl2 and 500 mg kg?1 of used engine oil to form the mixed soil contaminant. At the same concentration of chelates, EDTA was found to be more effective than EDDS in increasing the concentration of metal contaminants Cd and Pb in the plant. Compared to EDDS, EDTA was also more effective in promoting rhizodegradation of the organic contaminant formed by used engine oil. The study demonstrated that the application of chelates to soils containing mixed contaminants such as heavy metals (Cd and Pb) and organics (used engine oil) can simultaneously assist metal accumulation at higher concentrations in the biomass of Indian mustard plant and also reduce the amount of used engine oil in the soil through rhizodegradation.  相似文献   

11.
Siderophores are biogenic chelating agents produced in terrestrial and marine environments that increase the bioavailability of ferric iron. Recent work has suggested that both aqueous and solid-phase Mn(III) may affect siderophore-mediated iron transport, but scant information appears to be available about the potential roles of layer type manganese oxides, which are relatively abundant in soils and the oligotrophic marine water column. To probe the effects of layer type manganese oxides on the stability of aqueous Fe-siderophore complexes, we studied the sorption of ferrioxamine B [Fe(III)HDFOB+, an Fe(III) chelate of the trihydroxamate siderophore desferrioxamine B (DFOB)] to two synthetic birnessites [layer type Mn(III,IV) oxides] and a biogenic birnessite produced by Pseudomonas putida GB-1. We found that all of these predominantly Mn(IV) oxides greatly reduced the aqueous concentration of Fe(III)HDFOB+ at pH 8. Analysis of Fe K-edge EXAFS spectra indicated that a dominant fraction of Fe(III) associated with the Mn(IV) oxides is not complexed by DFOB as in solution, but instead Fe(III) is specifically adsorbed to the mineral structure at multiple sites, thus indicating that the Mn(IV) oxides displaced Fe(III) from the siderophore complex. These results indicate that layer type manganese oxides, including biogenic minerals, may sequester iron from soluble ferric complexes. We conclude that the sorption of iron-siderophore complexes may play a significant role in the bioavailability and biogeochemical cycling of iron in marine and terrestrial environments.  相似文献   

12.
In this study, we examined the movement of potassium (K) in columns of contaminated calcareous soils by sheep manure and ethylene diamine tetraacetic acid (EDTA). Glass tubes, 4.9 cm in diameter and 40 cm in length, were packed with contaminated soils. The resulting 20-cm long column of soil had a bulk density of 1.3–1.4 g cm−3. Columns were leached with distilled water, 0.01 M EDTA, 0.01 M CaCl2, and sheep manure extract solutions. The amounts of K leached varied considerably between different soils (sandy loam and loamy sand) and leaching solutions. The amount leached with EDTA solution, varied from 7.2 to 66.7% of the extractable K when 20 pore volumes had passed through the column. The breakthrough curves of K in the EDTA and CaCl2 were approximately similar, indicating they have similar ability to displace K from these contaminated calcareous soils. Thus, among leaching solutions application of EDTA and CaCl2 on contaminated soils might enhance the mobility of K and large amounts of K will be leached.  相似文献   

13.
The concentration and dynamic of soil trace metals in natural ecosystems, in particularly, is dependent on the lithology of parent rock as well as topography and geopedological processes. To ascertain more knowledge for this dependency, soils on three parent rocks involving peridotite, pegmatite, and dolerite in two contrasting topography aspects were investigated. The total values of Fe, Mn, Zn, Cu, and Ni were determined and compared for different soil pedons. The concentration of Fe, Mn, and Ni were highest in soils developed from peridotite (127, 1.8 g kg?1, and 218 mg kg?1, respectively), intermediate in soils derived from dolerite (81, 1.3 g kg?1, and 166 mg kg?1, respectively), and least in soil developed from pegmatite (50, 0.23 g kg?1, and 20 mg kg?1, respectively). The values of Zn and Cu, originated from different parent rocks, were in order of dolerite (78 mg kg?1) > peridotite (77 mg kg?1) > pegmatite (28 mg kg?1) and pegmatite (121 mg kg?1) > peridotite (111 mg kg?1) > dolerite (28 mg kg?1), respectively. For most of the studied pedons, profile metals distribution differed among the soils: The values of Fe, Cu, and Ni were enriched in the cambic horizons mainly as result of release, mobilization, and redistribution of the studied metals during geopedological processes, whereas those of Zn and Mn were concentrated in the surface horizons. Probably due to greater weathering rate of trace metal-bearing rocks on north-facing slope, the content of the trace metals along with the geoaccumulation index (I geo) and the degree of soil contamination (C d) were higher than on south-facing slope. Based on assessment of soil pollution indices, the soils were categorized as unpolluted [I geo ≤ 0 (class 0)], unpolluted to moderately polluted levels [0 < I geo < 1 (class 1)], and very low [C d < 1.5 (class 0)] to low degree of contamination [1.5 < C d < 2 (class 1)].  相似文献   

14.
Under and climate conditions the chemical weathering of manganese ores is govermed by the fugacities of O2,CO2 and S2 in the atmosphere and soils.Manganese minerals exhibit solid phase transformations without migration of Fe and Mn.Under tropical and subtropical humid climate condi-tions low-valent Mn is instable and apt to be oxidized into high valency state.High-valent Mn miner-als are stable and easy to form secondary high-grade Mn ores.Secondary concentration is possible for Mn ores in carbonate formations,while those in clastic rocks tend to migrate and may be washed away.Such differences are the main obstacles in prospecting Mn ore deposits.  相似文献   

15.
Oil fields present a potential ecological risk to nearby farmland soil. Here we present a new method designed to evaluate the ability of winter wheat (Triticum aestivum) to contribute to the dissipation of polycyclic aromatic hydrocarbons (PAHs), which are priority pollutants in soils contaminated by oily sludge. The influence of different doses of oily sludge on the dissipation of PAHs was studied along with individual PAH profiles in soils after different periods of plant growth. Five soil samples were artificially contaminated with different percentages of oily sludge (0 %, 5 %, 10 %, 15 % and 20 %). Winter wheat grew in the oily sludge–amended soils for 265 days. PAH content in the soils was monitored over the course of the study. The rate of PAH dissipation is related to the properties of different PAHs, period of winter wheat growth, and oily sludge application dose. Analysis for treated soils indicates that the dissipation of PAHs increased significantly over the first 212 days, followed by minimal changes over the final 53 days of treatment. In contrast, PAH dissipation slowed with increasing oily sludge application. For each PAH, the experimental results showed a significant compound-dependent trend. Winter wheat in the present study significantly enhanced the dissipation of PAHs in oily sludge–contaminated soil.  相似文献   

16.
Parallel electron energy-loss spectroscopy (PEELS) in a scanning transmission electron microscope (STEM) was used to record the Mn L2,3-edges from a range of natural and synthetic manganese containing materials, covering valences 0, II, III, IV and VII, with an energy resolution of ca. 0.5 eV. The Mn L2,3 electron-loss near-edge structure (ELNES) of these edges provided a sensitive fingerprint of its valence. The Mn2+ L2,3-edges show little sensitivity to the local site symmetry of the ligands surrounding the manganese. This is illustrated by comparing the Mn L2,3-edges from 4-, 6- and 8-fold coordinated Mn2+. In contrast, the Mn L3-edges from Mn3+ and Mn4+ containing minerals exhibited ELNES that are interpreted in terms of a crystal-field splitting of the 3d electrons, governed by the symmetry of the surrounding ligands. The Mn L3-edges for octahedrally coordinated Mn2+, Mn3+ and Mn4+ showed variations in their ELNES that were sensitive to the crystal-field strength. The crystal-field strength (10Dq) was measured from these edges and compared very well with published optically determined values. The magnitude of 10Dq measured from the Mn L3-edges and their O K-edge prepeaks of the manganese oxides were almost identical. This further confirms that the value of 10Dq measured at the Mn L3-edge is correct. Selected spectra are compared with theoretical 2p atomic multiplet spectra and the differences and similarities are explained in terms of the covalency and site symmetry of the manganese. The Mn L3-edges allow the valence of the manganese to be ascertained, even in multivalent state materials, and can also be used to determine 10Dq.  相似文献   

17.
Rhizosphere has different chemical and biological properties from bulk soils. Information about copper (Cu) desorption characteristics in the rhizosphere soils is limited. The objectives of this study were to determine Cu desorption characteristics and the correlation of its parameters with Cu extracted by DTPA-TEA, AB-DTPA and Mehlich 3 in bulk and rhizosphere amended soils with sewage sludge (10 g of sewage sludge was added to 1 kg soil) under greenhouse conditions in a rhizobox. The kinetics of Cu desorption in the rhizosphere and bulk was determined by successive extraction with DTPA-TEA in a period of 1 to 504 h at 25 ± 1 °C. The results showed that Cu extracted using several chemical extractants in the rhizosphere were significantly (P < 0.05) lower than in the bulk amended soils. In addition, Cu extracted using successive extraction in the rhizosphere were significantly (P < 0.01) lower than in the bulk soils. The best model for describing extraction data for the bulk and rhizosphere soils was the parabolic diffusion equation. Desorption kinetics of Cu conformed fairly well to first order and power function models. The results indicated that Cu diffusion rate in the wheat rhizosphere soils lower than in the bulk soils. Cu desorption rate in parabolic diffusion ranged from 0.326 to 0.580 mg kg?1 h?1/2 in the bulk soils, while it ranged from 0.282 to 0.490 mg kg?1 h?1/2 in the rhizosphere soils. Significant correlation (P < 0.05) between determine R values of parabolic diffusion and Cu desorption during 504 h with extracted Cu using DTPA-TEA, AB-DTPA and Mehlich 3 were found in the bulk and the rhizosphere soils. The results of this research revealed that Cu desorption characteristics in the wheat rhizosphere soils are quite different from bulk soils amended with sewage sludge.  相似文献   

18.
A surface-modified amorphous manganese oxide (SM-AMO) was prepared to increase the stability of a previously studied promising stabilizing agent and to compare its immobilizing efficiency with respect to contaminating metals with the original material. To synthesize the SM-AMO, the AMO surface was synthetically covered with a coating of MnCO3 because newly formed rhodochrosite precipitates were previously found to increase the stability of AMO particles in soils. A preliminary experiment evaluating the long-term stability of both materials in pure water suggested higher stability for the SM-AMO particles, showing a smaller release of Mn compared to the original AMO. An adsorption kinetics study focused on As, Cd, Pb and Zn showed lower adsorption rates and adsorption capacity for Zn, probably as a result of partial surface passivation. In comparison to these results for simple controlled systems, different effects were recorded when the two materials were applied to contaminated soils. When incubated in soil, a constantly lower mass loss was recorded in the case of SM-AMO. There were no significant differences in the release of Mn and DOC into the soil solution or in the stabilizing efficiency with regard to contaminating metal(loid)s between the original and surface-modified materials. Concerning the potential solid phase transformations in soil conditions, we observed a gradual equilibration between the surface composition of both materials. While the newly formed rhodochrosite precipitated on the AMO surface, the MnCO3 coatings on SM-AMO gradually dissolved. Both amendments also effectively supported microbial activity, especially in the more contaminated soil sample. Thus, despite the smaller mass loss, the effectiveness of both materials is comparable in the long term.  相似文献   

19.
Urban soil samples collected from the city of Xuzhou were analyzed by inductively coupled plasma mass spectrometry (ICP-MS) for Pb and Zn. The samples were also investigated for mineralogy using X-ray diffraction, thermal analyses and scanning electron microscopy (SEM). The identified minerals are mainly composed of quartz and calcite as major minerals. Soil samples contained elevated Zn (2,049 ± 5,439 mg/kg) and Pb (115 ± 58 mg/kg). According to the index of geoaccumulation, the soils of the study area are considered to be moderately to strongly contaminated with respect to Zn, moderately contaminated with respect to Pb. The magnetic measurements indicate that the dominant magnetic components are multidomain grains of ferrimagnetic minerals and that superparamagnetic and stable single-domain ferrimagnetic grains and non-ferrimagnetic minerals are present in small magnetic concentrations in this area. The measured metals correlated positively with the determined magnetic parameters (χ, χ ARM, SIRM and SOFT). This result suggests that simple, rapid, and non-destructive magnetic measurements could provide useful information about Pb and Zn pollution in Xuzhou urban surface soils.  相似文献   

20.
The distribution of Mn was examined in the bottom sediments and water column (suspended paniculate matter) of the Laurentian Trough. Gulf of St. Lawrence. A characteristic profile of Mn with depth in the sediment consisted of a Mn-enriched surface oxidized zone, less than 20 mm thick, and a Mn-depleted subsurface reducing zone. A subsurface Mn maximum occurred within the oxidized zone. Below this maximum the concentration dropped sharply to nearly constant residual levels in the reducing zone. The accumulating estuarine sediments are deficient in Mn compared to the river input of suspended matter and are definitely not the ultimate sink for manganese. Manganese escapes from the sediment by diffusion and resuspension, forming Mn-enriched, fine-grained particles which are flushed out in the estuarine circulation. 5.0 × 109gyr?1 of Mn, or 50% more than the river input of dissolved Mn. are exported to the open ocean. In spite of the efficient mobilization and export of Mn, the quantity exported is a small fraction (0.2%) of the total flux to the deep-sea sediments. This is related to the low levels of paniculate matter transported by the St. Lawrence River. The export phénomenon, however, is probably true of many coastal regions of muddy sediments and thus has interesting implications for the oceanic budget of Mn.  相似文献   

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