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1.
The kinetic curves of aluminum release from two variable charge soils and a kaolinite within 48 h can be divided into three stages: the first stage located within the initial 30 min, at which the release rate of Al was the fastest one and the released Al dominantly originated from exchangeable Al and amorphous Al pools. The Elovich equation fit the kinetics data at this stage fairly well. The moderate and the slow stages occurred within 0.5-2 and 2-48 h, respectively. During these two stages, the released Al was mainly attributed to Al oxides, poorly crystalline kaolinite and easily weathered hydrous mica. The different linear equations also fit the kinetics data at these two stages well. The rate of Al release decreased sharply with time during the fast stage, but the rate remained constant during the moderate and slow stages. In Ultisol, Al oxides were the more important pool for Al release than poorly crystalline kaolinite and easily weathered hydrous mica during the latter two stages. In Oxisol, poorly crystalline kaolinite was the more important Al pool. Compared to the control system, the presence of organic acids increased the rate and quantity of Al release from variable charge soils. The ability of organic acids to accelerate Al release followed the order: oxalic acid > citric acid > malic acid > lactic acid. This is generally in consistent with the magnitude of the stability constants of the Al-organic complexes. The release rate of Al also increased with the rise in concentration of organic acids.  相似文献   

2.
This study investigated the distribution and sources of Cd in soils from a Cd-rich area in the Three Gorges region, China. The results showed that in the study area arable soils contain 0.42–42 mg kg−1 Cd with 0.12–8.5 mg kg−1 in the natural soils, corresponding to high amounts of Cd (0.22–42 mg kg−1) in outcropping sedimentary rocks in the area. Both lognormal distribution and enrichment factor (EF) plots were applied in an attempt to distinguish between geogenic and anthropogenic origins of Cd in the local soils. The lognormal distribution plots illustrated that geogenic sources dominated in soils with low and moderate Cd concentrations (<8.5 mg kg−1), whereas anthropogenic sources (agricultural activities, coal mining) significantly elevated Cd contents in some arable soils (>8.5 mg kg−1). The enrichment factor plots illustrated that the majority of the soil samples had EF values of <5, pointing to a geogenic origin of Cd in the soils, whereas some arable soils had EF values >5, pointing to an additional anthropogenic input of Cd to the soils. Sequential extraction results showed that Cd soluble in water and weak acid (water-soluble, exchangeable and carbonate fraction of the soil) accounts for an average of 31% of the total soil Cd, which indicates high potential for Cd mobility and bioavailability. The findings point to a potential health risk from Cd in areas with high geogenic background concentrations of this metal.  相似文献   

3.
Organic P (OP) plays an important role in soil P cycling and is a potential P source for wetland plants. In this study, a modified chemical sequential fractionation method and 31P nuclear magnetic resonance spectroscopy (31P NMR) of NaOH–EDTA extracts were used to examine the distribution of organic P fractions and compounds in soil profiles of the Beijing Yeyahu Wetland, China. The influence of acid treatment prior to NaOH–EDTA extraction on 31P NMR spectra was also investigated. Results show that highly resistant OP was the major class of organic P. The rank order of organic P fractions was highly resistant OP (on average accounting for 68.5% of total OP) > moderately resistant OP (15.8%m of total OP) > moderately labile OP (11.4% of total OP) > labile OP (4.3% of total OP). Most of the organic P fractions decreased with soil depth due to the accumulation of plant residues in surface soils and the deposition and diagenesis of soils. Moderately (r = 0.586, p < 0.01) and highly (r = 0.741, p < 0.01) resistant OP fractions were positively correlated with soil organic matter. Phosphorus compounds including orthophosphate (23–74.6% of total P in spectra), monoester phosphate (18.6–76%), diester phosphate (nil-7.8%) and pyrophosphate (nil-6.7%) were characterized using 31P NMR. Monoester-P was the dominant soil organic P compound identified. The proportion of monoester-P increased significantly in NaOH–EDTA extracts with HCl pretreatment and it was confirmed by chemical analysis. Therefore, it can be concluded that HCl pretreatment can remove more than half of the inorganic P and increase the overall recovery rate of organic P during subsequent NaOH–EDTA extraction, which might be a new approach for organic P detection. Furthermore, the OP chemical sequential fractionation method presented in this study is an integrated and comprehensive approach which can be used for further verification.  相似文献   

4.
The bioavailability of metals and their potential for environmental pollution depends not simply on total concentrations but on their chemical form. Consequently, knowledge of aqueous metal speciation is essential in investigating potential metal toxicity and mobility. Dissolved (<1 kDa), colloidal (1 kDa–0.45 μm) and particulate (>0.45 μm) size fractions of sulfate, organic C (OC) and 18 metals/metalloids were investigated in the extremely acidic Vörå River system in Western Finland, which is strongly affected by acid sulfate (AS) soils. In addition, geochemical modelling was used to predict the formation of free ions and complexes in these acidic waters. The most important finding of this study is that the very large amounts of elements known to be released from AS soils (including Al, Ca, Cd, Co, Cu, Mg, Mn, Na, Ni, Si and U) occur and can prevail mainly in toxic forms throughout acidic river systems; as free ions and/or sulfate-complexes. This has serious effects on the biota and particularly dissolved Al can be expected to have acute effects on fish and other organisms. In the study area, only the relatively forested upstream area (higher pH and contents of OC) had significant amounts of a few bioavailable elements (including Al, Cu, Ni and U) due to complexation with the more abundantly occurring colloidal OC in the upstream area. It is, however, notable that some of the colloidal/particulate metals were most likely associated with metal bearing phyllosilicates eroded from clay soils. Moreover, the mobilisation of Fe and As was small and As was predicted to be associated with Fe oxides, indicating a considerable influence of Fe oxides on the mobilisation/immobilisation processes of As. Elements will ultimately be precipitated in the recipient estuary, where the acidic metal-rich river water will gradually be diluted/neutralised with brackish seawater in the Gulf of Bothnia. According to speciation modelling, such a pH rise may first cause precipitation of Al, Cu and U together with organic matters closest to the river mouth, in line with previous sediment studies from the estuary.  相似文献   

5.
Iron mobilisation from aquifer rocks in an important fractured aquifer system in South Africa is resulting in clogging of boreholes by Fe oxide minerals. Leach experiments using natural waters were conducted to determine the effects of redox conditions, pH lithology and presence of organic acids on the rate and extent of Fe dissolution from aquifer rocks, with the aim of clarifying the association of Fe clogging with geological formations that show Fe staining on weathering. The results indicate that the greatest amount of Fe (>30 mmol/kg rock) is leached from arenaceous rocks with low total Fe contents (49.0–75.0 mmol/kg) under anoxic conditions. Rocks with the highest Fe contents (>800 mmol/kg) generated low concentrations of Fe (<10 mmol/kg) even under favourable conditions of 0 mg/L DO and pH 3. The extent of Fe dissolution from the rocks was found to be most strongly dependent on the redox conditions, and the form of Fe present in the rock, with ascorbate-extracted amorphous Fe being the most mobile. The rate of dissolution is affected by pH and the presence of natural organic acids in the leachate. However, the effect of organic acids was only noticeable on arenaceous rocks.  相似文献   

6.
Carbon isotope compositions for the 20 standard amino acids are calculated using high-level molecular orbital and density functional theory methods. In agreement with measurements of the isotopic compositions of amino acids in a cyanobacterium [Macko, S.A., Fogel, M.L., Hare, P.E., Hoering, T.C., 1987. Isotope fractionation of nitrogen and carbon in the synthesis of amino acids by microorganisms. Chemical Geology 65, 79–92] the calculations give heavy signatures for aspartic acid + asparagine, serine, glutamine + glutamic acid and light signatures for leucine and isoleucine. The relative intramolecular enrichment of 13C in carboxyl groups is often much less than measured [Abelson, P.H., Hoering, T.C., 1961. Carbon isotope fractionation in formation of amino acids by photosynthetic organisms. Proceedings of the National Academy of Sciences, USA 47, 623–632]. Fractionations predicted from density functional calculations often differ by several per mil from those predicted from molecular orbital calculations.  相似文献   

7.
Serpentinite rocks, high in Mg and trace elements including Ni, Cr, Cd, Co, Cu, and Mn and low in nutrients such as Ca, K, and P, form serpentine soils with similar chemical properties resulting in chemically extreme environments for the biota that grow upon them. The impact of parent material on soil characteristics is most important in young soils, and therefore the incipient weathering of serpentinite rock likely has a strong effect on the development of serpentine soils and ecosystems. Additionally, porosity generation is a crucial process in converting rock into a soil that can support vegetation. Here, the important factors affecting the incipient weathering of serpentinite rock are examined at two sites in the Klamath Mountains, California. Serpentinite-derived soils and serpentinite rock cores were collected in depth profiles from each sampling location. Mineral dissolution in weathered serpentinite samples, determined by scanning electron microscopy, energy dispersive spectrometry, electron microprobe analyses, and synchrotron microXRD, is consistent with the order, from most weathered to least weathered: Fe-rich pyroxene > antigorite > Mg-rich lizardite > Al-rich lizardite. These results suggest that the initial porosity formation within serpentinite rock, impacting the formation of serpentine soil on which vegetation can exist, is strongly affected both by the presence of non-serpentine primary minerals as well as the composition of the serpentine minerals. In particular, the presence of ferrous Fe appears to contribute to greater dissolution, whereas the presence of Al within the parent rock appears to contribute to greater stability. Iron-oxidizing bacteria present at the soil–rock interface have been shown in previous studies to contribute to the transition from rock to soil, and soils and rock cores in this study were therefore tested for iron-oxidizing bacteria. The detection of biological iron oxidation in this study indicates that the early alteration of these Fe-rich minerals may be mediated by iron-oxidizing bacteria. These findings help provide insight into the incipient processes affecting serpentinite rock weathering, important to the development of extreme serpentine soils and the biota that grow on them.  相似文献   

8.
Seafloor sediment containing biogenic amino acids was heated with NaCl solutions at 50–200 °C for 240 h to investigate the dissolution process of amino acids and evaluate their stabilities under hydrothermal conditions. Dissolved amino acids in the combined phase (dissolved combined amino acids, DCAAs) and free phase (dissolved free amino acids, DFAAs) were rapidly released into the solution during heating. The amount of DCAAs in the solutions was 4–9 times higher than the amount of DFAAs at each temperature. When heated at ⩽ 100 °C, most of the total dissolved hydrolyzable amino acids (TDHAAs) were in the combined form (DCAAs/TDHAAs ratios > 0.9). The compositions of the DCAAs in solutions heated at ⩽ 100 °C were similar to that of the total hydrolyzable amino acids (THAAs) of the initial sediment, indicating that the DCAAs, which are derived from organisms and biodebris in the sediment, are barely altered during the hydrothermal reaction at these temperatures. On the other hand, the DCAAs/TDHAAs ratios were 0.72 and 0.57 at 150 and 200 °C, respectively, and the compositions of the DCAAs at 150 and 200 °C were significantly different from that of the initial THAAs. In addition, non-protein amino acids (β-alanine and γ-aminobutyric acid), which are sensitive biochemical indicators of the diagenetic alteration of natural organic matter, drastically increased to 80.9% of the DCAAs after heating at 200 °C. These results suggests that DCAAs are thermally unstable in the hydrothermal solutions at ⩾ 150 °C. These DCAA would be transformed into thermally stable geo-polymers such as humic-like substances and hydrolyzable kerogens.  相似文献   

9.
Batch sorption isotherms of two nonpolar compounds (1,3-dichlorobenzene and 1,3,5-trichlorobenzene) and two polar compounds (1,3-dinitrobenzene and 1,3,5-trinitrobenzene) to heated (at 375 °C for 24 h) and unheated coals (lignite and anthracite) were compared with those to a soil humic acid and a maize stalk derived biochar. For all test compounds, unheated lignite and anthracite exhibited much stronger sorption than humic substances (the organic carbon-normalized distribution coefficient was up to 2–3 orders of magnitude larger), but lower sorption than biochar. This sorption trend is consistent with the degree of sorbent condensation (biochar > coal > humic acid). The results indicate that sorption of the test sorbates (regardless of the difference in polarity) to soils would be dominated by carbonaceous geosorbents. Notably, the organic carbon contents of the coals were pronouncedly lowered by the heat treatment, from 47.4% to 7.3% for lignite, and from 80.1% to 58.1% for anthracite. Moreover, the heat treatment markedly decreased organic carbon-normalized distribution coefficient to coals (up to one order of magnitude), attributable to the decreased hydrophobicity of sorbents due to increased O-containing groups from oxidation. An important implication is that heat treatment, which is commonly used to quantify the content of carbonaceous geosorbents in soil and sediment, may cause significant underestimation of sorption contribution of carbonaceous geosorbents due to the combined effect of reduced organic carbon content and decreased hydrophobicity of less graphitized carbonaceous geosorbents (coals). This was illustrated using a widely adopted dual-component model that combines linear partition to humic substances (represented by humic acid) and nonlinear adsorption on condensed geosorbents (represented by biochar and coal).  相似文献   

10.
Weathering of basaltic ash in volcanic areas produces andosols, rich in allophane and ferrihydrite. Since the rate of mineral formation is very useful in climate and geochemical modelling, this study investigates Si isotope compositions of allophane as a proxy for mineral formation. Allophane formed in contrasting conditions in five Icelandic soil profiles displays silicon isotope signatures lighter than the basalt in less weathered soils (?0.64 ± 0.15‰), and heavier in more weathered organic-rich soils (+0.23 ± 0.10‰). The fate of the dissolved Si in those volcanic soils strongly depends on Al availability. In organic-rich soils, most of Al is humus-complexed, and the results support that Si precipitates as opaline silica by super-saturation, leaving an isotopically heavier dissolved Si pool to form allophane with uncomplexed Al. This study highlights that Si isotopes can be useful to record successive soil processes involved in mineral formation, which is potentially useful in environmental paleo-reconstruction.  相似文献   

11.
This study was conducted to assess the anthropogenic impact on metal concentrations in the bottom sediments of the Juam reservoir, Korea, and in stream sediments in its catchment, and to estimate the potential mobility of selected metals (Fe, Mn, Cu, Ni, Pb and Zn) using sequential extraction. A comparison of the metal concentrations in the stream sediments with mean background values in sediments collected from first- or second-order creeks shows that Pb, Cu and Ni are the most affected by anthropogenic inputs. The 206Pb/207Pb ratios of the bottom and core sediments (means: 1.2320 ± 0.0502 and 1.2212 ± 0.0040, respectively) suggest that Pb contamination is mainly due to the waste discharge of abandoned coal and metal mines rather than industrial and airborne sources. Considering the proportion of metals bound to the exchangeable, carbonate and reducible fractions, the comparative mobility of metals is suggested to decrease in the order Mn > Pb > Zn > Ni > Fe ≫ Cu.  相似文献   

12.
《Applied Geochemistry》2006,21(7):1093-1108
Peña del Hierro is an abandoned mine site located in the catchment area of the Tinto river (Pyrite Belt, SW Spain). As leaching from the spoils affect the quality of the stream water, the waste dumps have been characterized for mineralogy, geochemistry and granulometry to obtain an estimate of the potential pollution. Waste rock dumps in Peña del Hierro are very heterogeneous and are mainly composed of acid volcanic tuffs > gossan > shales > roasted pyrite ashes > floated pyrite. The volcanic tuffs, the gossan and the shales coexist in the same piles. The roasted pyrite ashes and the floated pyrite form more homogeneous dumps. The dissolution of pyrite concentrated in pyrite ashes and floated pyrite units can generate acid mine drainage. Nevertheless, acid volcanic tuffs, which are rich in pyrite and have no neutralizing minerals, are the main source of these acidic effluents. Only muscovite might partially neutralize the acidity, but the dissolution of this mineral is too slow to compensate for acidity. The occurrence of jarosite in the <2 mm fraction indicates that extreme acid mine drainage occurs. The gossan and roasted pyrite ashes have high contents of trace elements. According to their concentration, As (46–1710 ppm), Pb (113–3455 ppm) and Hg (0–53) are some of the most important toxic trace elements in these wastes. In dumps mainly composed of volcanic tuffs most of the trace elements derive from the gossan mixed in the piles. Gossan is stable in an oxidizing environment, but acidic effluents (pH < 2) can dissolve Fe oxyhydroxides from them and release high amounts of trace elements to the stream water. This research contributes to estimating the production of acid mine drainage and the actual contamination risk of potentially toxic elements in soils and waters of this area, and could be the base for possible future mitigation actions in other areas affected by mining wastes.  相似文献   

13.
Heavy metals having both natural and anthropogenic origin are common contaminants in soils and sediments, and can be transferred and bioaccumulated at all levels of the food chain, posing serious environmental concern to the local population. In this paper, agricultural soils from the Province of Ferrara (easternmost part of the Padanian Plain, northern Italy) were investigated to assess the levels of potentially toxic metals in relation to their phytoavailability. Agricultural soils have been sampled in order to identify the origin, mobility and bioavailability of heavy metals, collecting superficial and deeper (depths of 20–30 and 100–120 cm, respectively) horizons. The “total” XRF analyses properly elaborated with a statistical approach reveal that soils evolved from two distinct types of alluvial sediments, in turn related to the Po and Reno rivers; the former type is distinctively enriched in heavy metals (particularly Cr and Ni), reflecting the presence of femic and ultrafemic rocks in the hydrological basin of River Po. The absence of Top Enrichment Factors for Ni, Co, Cr, V, and Pb suggests that the content of these elements is natural and unaffected by contamination, whereas superficial enrichments of Cu (and Zn) is ascribed to anthropogenic inputs related to agricultural activities. Multiple extraction tests using variously aggressive reactants (aqua regia, DTPA, EDTA, NH4NO3, and H2O) analyzed by ICP gave insights on the specific mobility of the distinct elements, which decreases in the following order: Pb > Cu > Cd > Co > >Ni > Cr. Taking into consideration the elements that are inducing the main concerns, Cr appears scarcely mobile, whereas Ni could be more phytoavailable and has to be monitored in the local agricultural products. Cd although scarcely abundant has to be monitored for its mobility and toxicity, whereas Cu although abundant and extremely mobile doesn’t induce concerns as it is not hazardous for the living receptors.  相似文献   

14.
The aim of this study was to investigate the dissolution and transformation characteristics of phyllosilicate under low molecular weight organic acids in the farmland environment (pH 4.0–8.0). Changes of dissolution and morphology of biotite were evaluated using chemical extraction experiments and in situ/ex situ atomic force microscopy (AFM) with fluids of citric acid (CA) solution at pH 4.0, 6.0, and 8.0. Results of extracting experiments show that CA solutions contributed to the release rate of potassium (K), silicon (Si), and aluminum (Al) from biotite relative to a control aqueous solution. In situ AFM observations indicate that the dissolution of biotite from the biotite (0 0 1) surface occurred on the terrace, segment, and fringe of pits, while new etch pits did not readily form on biotite (0 0 1) surfaces in aqueous solutions. However, dissolution rates of terraces can be greatly accelerated with the help of citrate. In pH 4.0 CA solution, 70 min dissolution reactions of biotite (0 0 1) surfaces result in more etch pits than in pH 6.0 and 8.0 solutions. In addition, the transformation of biotite occurred simultaneously with the dissolution process. Secondary coating was observed on the biotite (0 0 1) surface after 140 h of immersion in a weak acid environment. Thus, the protons have a dominant role in the dissolution process of biotite with organic (carboxyl) acting as a catalyst under acidic condition. Based on the theory of interactions on a water–mineral interface in a weak acid environment, dissolution of biotite starts from defect/kink sites on the surface, one layer by one layer, and develops along the [h k 0] direction. A secondary coating that forms on the biotite (0 0 1) surface may restrain the formation and growth of etch pits, whereas this process may have a positive role on the stability of soil structure during long-term soil management.  相似文献   

15.
Trace element contents and distributions in authigenic quartz cement in deeply buried (2500–4000 m) Haushi Group sandstones from wells in Oman have been investigated in order to determine the factors that control trace element uptake during precipitation.Scanning electron microscope-cathodoluminescence images show well developed growth zones within the quartz cement, which correlate with chemical zonations observed in electron microprobe Al distribution maps. The most abundant trace elements are Al (50–3000 μg g?1), Li (1–100 μg g?1), Na (1–40 μg g?1), and Ge (0.3–5 μg g?1) with a strong linear correlation between Li and Al and a weaker one between Ge and Al. The molar concentration of Li (+ Na) accounts only for ~ 15% of the charge compensation for Al3+ substitution of Si4+. Though H was not measured in this study, these data indicate a major role of H in charge balancing Al3+. The samples belong to the same stratigraphic unit and have similar petrography, but show considerable variability in absolute trace element concentrations between different wells. This variability does not correlate with either sample depth or temperature and shows no regional pattern, but seems to reflect petrophysical and tectonic differences within the sedimentary basin.Petrographic observations of the cogenetic mineral assemblages and hydrochemical modelling indicate that a change from the equilibrium assemblage quartz–kaolinite (–dolomite) to quartz–illite (–dolomite) reflects a decrease in the CO2 concentration and concurrent variations of the Al concentration. It is concluded that changes in the CO2 concentrations are responsible for fluctuations in fluid Al concentrations and thus likely also in the investigated quartz cements.  相似文献   

16.
《Gondwana Research》2010,17(3-4):622-632
Peculiar magmatic rocks were erupted and emplaced at depth at the margin of the Gondwana supercontinent during the Cambro-Ordovician transition. These rocks are characterized by high contents in silica and iron but they do not have equivalents in the high-silica members of the calc-alkaline series. They have particular geochemical signatures, with Al saturation index, ASI > 1, FeO > 2.5 wt.%, MgO > 0.8 wt.% for very low contents in calcium (CaO < 2.0 wt.%), supporting a derivation from near-total melting (> 80 vol.% melt) of metagreywackes. The results from inverse experiments indicate that the most plausible conditions are within the range 1000 °C (excess water) and 1100–1200 °C (subsaturated and dry) at pressures of 1.5 to 2.0 GPa. A tectonic scenario implying melting of subducted sediments within an ascending mantle-wedge plume is suggested for the generation of primary ferrosilicic melts at the Gondwana continental margin during Upper Cambrian to Lower Ordovician times.  相似文献   

17.
Black carbon (BC) is a poorly understood type of organic carbon but it is present in almost all environmental systems (i.e., atmosphere, soil and water). This work focuses on soot BC in desert soils and, in particular, urban soils from the Phoenix, Arizona metropolitan area. Soot BC is that fraction of black carbon formed from the condensation of gas phase molecules produced during burning. Soot BC in Phoenix area soils exhibits a range in both concentration and isotopic composition. Soot BC concentration in 52 soils (desert, agricultural and urban) ranges from 0.02–0.54 wt% and comprises from < 1 to as much as 89% of the soil organic carbon (OC). Soot BC concentrations are higher in urban soils than in desert or agricultural soils. The average isotopic composition of soot BC is −18‰ ± 3‰; this is an enrichment of 5.5‰ relative to bulk soil organic carbon. The distribution in concentration and variation in isotopic composition across the study area suggests soot BC in this arid-land city has multiple sources, including a significant fossil fuel component.  相似文献   

18.
The Xiadong Alaskan-type complex shares much in common with typical Alaskan-type complexes worldwide, while showing some unique features in terms of mineral compositions. Olivine from the Xiadong dunites is characterized by extremely high Fo component of 91.7–96.7 and anomalously negative correlation of Fo with NiO, while chromite is featured by high 100 × Fe3+/(Fe3+ + Cr + Al) (>70), high 100 × Fe2+/(Fe2+ + Mg) (>70), high 100 × Cr/(Cr + Al) (>90), low MnO (<0.6 wt%) and TiO2 contents (<0.5 wt%). To investigate these particular features, we conducted petrographic observation and mineral composition analyses for the Xiadong dunite. A number of Fe and/or Ni sulfides and alloys occurring as inclusions in olivine and chromite indicate that base metal mineral segregation took place prior to crystallization of olivine and chromite and probably induced Fe and Ni depletions in olivine. The FeO and MgO variations in profile analyses from chromite to adjacent olivine are compatible with Fe-Mg exchange. The diffusion mechanism of Fe from olivine to chromite and Mg from chromite to olivine may have elevated both Fo of olivine and 100 × Fe2+/(Mg + Fe2+) ratio of chromite and further enhanced the decoupling of Fo and NiO in olivine. We thus suggest that base metal mineral segregation and Fe-Mg exchange play important roles in the extreme compositions of the Xiadong dunite. The Ni depletion of olivine and degree of Fe-Mg exchange between olivine and chromite may be used as indicators of mineralization in mafic-ultramafic intrusions.  相似文献   

19.
Black carbon (BC), especially biochar, is a potential material for the remediation of hydrophobic organic compounds (HOCs) pollution in soils and sediments. Recent studies have reported that the adsorption capability of BC in sediment was reduced as time increased. It was hypothesised that this behaviour was caused by the presence of natural organic matter (NOM), but few systematic studies have examined the influence of NOM on the sorption ability of BC in sediment (S). The results of this study revealed that a humic acid (HA) coating changed the surface properties, blocked the micropores, and decreased the sorption capacity of rice-straw biochar (RBC) towards pentachlorophenol. With increasing aging time, the reductions in the sorption capacity of the S + RBC and S + HA + RBC systems occurred more rapidly than in the S + HA/RBC (HA-coated RBC) system, and the sorption curves became closer to that of the S + HA/RBC system, indicating that HA may play a primary role in reducing the sorption capacity of RBC in the sediment. With higher HA contents, the sorption capacity of the complex sediments was lower and decreased more rapidly.  相似文献   

20.
The Mn-Ba-Pb deposit at Aspro Gialoudi in NW Milos is shown to be a fossil inhalative-exhalative hydrothermal deposit that represents the deepest part of the Vani succession at the western extremity of the main Vani manganese deposit. The geology of the Vani-Aspro Gialoudi area is characterized by Upper Pliocene-Lower Pleistocene dacitic and rhyodacitic lava domes, which are overlain by the Vani volcaniclastic unit considered to be part of the 2.66–1.44 Ma magmatic event at Milos Island. The presence of in-situ and intrusive hyaloclastite breccias surrounding the coherent lava domes at Aspro Gialoudi and Vani areas indicates submarine emplacement for the domes. The dacitic-rhyodacitic domes are variously altered (mainly propylitic and/or argillic alteration, silicified and in some cases locally exhibiting adularia alteration). Both Aspro Gialoudi and main Vani deposit are located proximal to fault systems: the main Vani manganese deposit is adjacent to the NW-trending Kondaros-Katsimouti-Vani Dome fault, whereas the Aspro Gialoudi deposit is adjacent to the relatively minor NE-trending fault on the west coast of Milos. At Aspro Gialoudi, mineralization took place in a subseafloor and/or seafloor environment and is characterized by a stratabound Mn-barite-rich deposit mainly within a package of propylitized intrusive hyaloclastites and within the overlying sandstones. Banded epithermal veins trending NE-SW and composed of chalcedonic silica/quartz + barite + Mn-oxide ± sulfides crosscut the dacitic lavas, the hyaloclastites and the overlying volcaniclastic sequence at Aspro Gialoudi and are considered to represent the feeder zones of the manganese-barite mineralization. Within the veins, early sulfide (galena-sphalerite) barite and quartz deposition is followed by manganese oxides and aragonite, thus resembling the epithermal-style Pb-Zn-Ag-Mn mineralization across the NW-trending Katsimoutis-Kondaros-Vani fault. Mineralization in Aspro Gialoudi and Vani deposits seems to be controlled by alternating cycles of deposition of sulfides and hydrothermal manganese oxides within the faults. Manganese deposition in both deposits formed in a similar manner, namely by transport of hydrothermal fluids through the adjacent fault systems into a reservoir of volcanoclastic sandstone and hyaloclastites to produce a deposit initially consisting of principally of pyrolusite and occasionally ramsdellite, which were subsequently replaced by cryptomelane, hollandite, coronadite and hydrohaeterolite. Precipitation of hydrothermal manganese oxides took place very quick and under microbial Mn(II) oxidation. Compositional data show that metallic elements most enriched in the Aspro Gialoudi and Vani manganese deposits relative to the average continental crust, lie in the sequences Pb > Cd > Mn > As > Sb > Zn > W > Tl > Ba > Cu > Mo > Co > Bi and As > Sb > Pb > Mn > Tl > Cd > Zn > W > Cu > Ba > Mo > Co, respectively. Mineralogical and geochemical (e.g. REE) data from both Aspro Gialoudi and main Vani deposit are taken to indicate mainly a seawater source for the hydrothermal fluids. These two deposits are genetically and spatially related to base- and precious metal intermediate-sulfidation epithermal mineralization. They formed successively by similar processes and are considered to be integral parts of the same hydrothermal system.  相似文献   

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