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1.
有机酸对高岭石, 针铁矿和水铝英石吸附镉的影响   总被引：12，自引：0，他引：12  
LIAO Min 《土壤圈》2006,16(2):185-191
Effects of organic acids （oxalic, acetic, and citric） on adsorption characteristics of Cadmium （Cd） on soil clay minerals （kaolinite, goethite, and bayerite） were studied under different concentrations and different pH values. Although the types of organic acids and minerals were different, the effects of the organic acids on the adsorption of Cd on the minerals were similar, i.e., the amount of adsorbed Cd with an initial solution pH of 5.0 and initial Cd concentration of 35 mg L^-1 increased with increasing concentration of the organic acid in solution at lower concentrations, and decreased at higher concentrations. The percentage of Cd adsorbed on the minerals in the presence of the organic acids increased considerably with increasing pH of the solution. Meanwhile, different Cd adsorption in the presence of the organic acids, due to different properties on both organic acids and clay minerals, on kaolinite, goethite, or bayerite for different pHs or organic acid concentrations was found.  相似文献   

2.
Oxalic acid plays an important role in improving the bioavailability of soil nutrients. Batch experiments were employed to examine the influences of oxalic acid on extraction and release kinetics of potassium （K） from soils and minerals along with the adsorption and desorption of soil K^＋. The soils and minerals used were three typical Chinese soils, black soil （Mollisol）, red soil （Ultisol）, and calcareous alluvial soil （Entisol）, and four K-bearing minerals, biotite, phlogopite, muscovite, and microcline. The results showed that soil K extracted using 0.2 mol L^-1 oxalic acid was similar to that using 1 mol L^-1 boiling HNO3. The relation between K release （y） and concentrations of oxalic acid （c） could be best described logarithmically as y = a ＋ blogc, while the best-fit kinetic equation of K release was y = a ＋ b√t, where a and b are the constants and t is the elapsed time. The K release for minerals was ranked as biotite 〉 phlogopite 〉〉 muscovite 〉 microcline and for soils it was in the order： black soil 〉 calcareous alluvial soil 〉 red soil. An oxalic acid solution with low pH was able to release more K from weathered minerals and alkaline soils. Oxalic acid decreased the soil K^＋ adsorption and increased the soil K^＋ desorption, the effect of which tended to be greater at lower solution pH, especially in the red soil.  相似文献   

3.
Two soils, one consisting of 1：1 clay minerals at pH 4.5 and the other containing 2：1 clay minerals at pH 7.0, were used to estimate the conversion of added NH4^＋ under different C/N ratios （glucose as the C source） and the addition of potassium. Under lower C/N ratios （0：1 and 5：1）, a large part of the added NH4^＋ in the acid soil was held in the forms of either exchangeable or water soluble NH4^＋ for a relatively long time and under higher C/N ratio （50：1）, a large amount of the added NH4^＋ was directly immobilized by microorganisms. In the second soil containing appreciable 2：1 type clay minerals a large part of the added NH4^＋ at first quickly entered the interlayer of the minerals under both lower and higher C/N ratios. In second condition, however, owing to microbial assimilation stimulated by glucose the newly fixed NH4^＋ could be completely released in further incubation because of a large concentration gradient between external NH4^＋ and fixed NH4^＋ in the mineral interlayer caused by heterotrophic microorganisms, which imply the fixed NH4^＋ to be available to plants. The results also showed that if a large amount of K＋ with carbon source together was added to soil, the higher K＋ concentration of soil solution could impede the release of fixed NH4^＋, even if there was a lot of carbon source.  相似文献   

4.
根瘤菌存在下土壤胶体和矿物对镉的吸附   总被引：8，自引：2，他引：6  
Experiments were conducted to study the adsorption of Cd on two soil collids(red soil and yellowbrown soil) and three variable-charge minerals (goethite,noncrystalline Fe oxide and kaolin) in the absence and presence of rhizobia.The tested strain Rhizobium fredii C6,tolerant to 0.8 mmol L^-1 Cd,was selected from 30 rhizobial strains.Results showed that the isotherms for the adsorption of Cd by examined soil colloids and minerals in the presence of rhizobia could be described by Langmuir equation.Within the range of the numbers of rhizobial cells studied,the amount of Cd adsorbed by each system increased with increasing rhizobial cells,Greater increases for the adsorption of Cd were found in red soil and kaolin systems.Rhizobia influence on the adsorption of Cd by examined soil colloids and minerals was different from that on the adsorption of Cu.The presence of rhizobia increased the adsorption affinity of soil colloids and minerals for Cd,particularly for the goethite and kaolin systems.The discrepancies in the influence of rhizobia on the adsorbability and affinity of selected soil colloids and minerals for Cd suggesed the different interactions of rhizobia with various soil components.It is assumed that bacterial biomass plays an important role in controlling the mobility and bioavailability of Cd in soils with kaolinite and goethite as the major colloidal compnents,such as in variable-charge soil.  相似文献   

5.
湿润速率和粘粒含量对红壤沟间侵蚀的影响   总被引：4，自引：0，他引：4  
An aggregate stability test and a simulated rainfall test were conducted on four representative Ultisols from southeastern China. The soils selected, with clay contents ranging between 117 and 580 g kg-1 , were derived from shale and Quaternary red clay. The stability of aggregates (2–5 mm in diameter) obtained from the soil samples were determined by the Le Bissonnais method. For determination of infiltration, runoff, and erosion, the soil samples were packed in 30 cm × 60 cm trays, wetted at rates of 2, 10, and 60 mm h-1 , and then exposed to simulated rainfall at 60 mm h-1 for 1 h. The results indicated that both aggregate stability and slaking caused by fast wetting increased with increasing clay content. The effect of wetting rate (WR) on infiltration and seal formation varied with clay contents. In the soil with low clay content (sandy loam), the infiltration rate was affected slightly by WR due to low aggregate stability and slaking. In the soils with medium clay content (silt clay loam and clay), WR affected infiltration significantly due to the high aggregate slaking force. In the soil with high clay content, the effect of WR on infiltration was significant, but not as evident as in the soils with medium clay content, which may be related to high aggregate stability by wetting partially compensating for slaking force. The effect of WR on soil loss was similar to that of runoff, but more pronounced. The findings from this study indicated that the relationship between wetting rate and clay content should be considered when predicting interrill erosion in Ultisols.  相似文献   

6.
The particle-size distribution and mineralogical composition of the clay (< 2 μm) and fine-sand (0.25--0.10 mm) fractions in soils of two inland valleys in Abakaliki and Bende, Southeast Nigeria, were investigated to provide basic information on soil-forming processes and agricultural potentials. These soils were silty or clayey, deriving from Cretaceous or Tertiary shale materials. The particle-size distribution and its computation on a clay-free basis revealed relatively remarkable lithologic breaks in a couple of pedons. The effect of lithologic discontinuities on soil mineralogical composition was not, however, conspicuous. Petrographic investigation revealed that quartz predominantly comprised the fine-sand fraction in the soils at both study sites. Nevertheless, the clay mineralogical composition of the soils was a mixture of kaolinite, irregularly interstratified smectite-illite intergrades (S/I), hydroxyl-Al interlayered 2:1 type clays (HICs), vermiculite, smectite, halloysite and illite along with fine-sized quartz in Abakaliki. The soils of Bende predominantly contained smectite, which was partially interlayered with hydroxyl-Al and kaolinite. It is suggested that seasonal floodwater has slowed the disintegration of weatherable clay minerals inherited from the shale, while quartz originating from the sandstone is predominant in the fine-sand fraction. Additionally, a possible soil-forming process observed at the both study sites was ferrolysis, which was indicated by a clear decreasing pattern of HICs downward in the soil profiles. The entry of S/I and vertical distribution patterns for a couple of clay minerals in the pedon suggested that the soils in Abakaliki have developed under the significant influence of aeolian dust delivered by the harmattan. The findings might describe a site-specific deposition pattern of harmattan dusts as well as hydromorphic soil-forming processes in the wetlands of the inland valleys.  相似文献   

7.
Alfalfa cropping has been considered an efficient method of increasing soil fertility.Usually nitrogen increase in root nodules is considered to be the major beneficial effect.A 21-year time series (five sampling periods) of alfalfa cultivation plots on a loess soil,initially containing illite and chlorite,in Lanzhou of northwestern China was selected to investigate the relationships among alfalfa cropping,soil potassium (K) content and soil clay minerals.The results indicated that soil K significantly accumulated after cropping,with a peak value at about 15 years,and decreased afterwards.The accumulated K was associated with the K increase in the well-crystallized illite,which was not extracted by the traditional laboratory K extraction methods in assessing bioavailability.The steep decline in soil K content after 15-year cropping was in accord with the observed fertility loss in the alfalfa soil.Plant biomass productivity peaked at near 9 years of culture,whereas soil K and clay minerals continued to increase until cropping for 15 years.This suggested that K increased in the topsoil came from the deep root zone.Thus alfalfa continued to store K in clays even after peak production occurred.Nitrogen did not follow these trends,showing a general decline compared with the native prairie soils that had not been cropped.Therefore,the traditional alfalfa cropping can increase K content in the topsoil.  相似文献   

8.
Aggregation and structure play key roles in water-holding capacity and stability of soils.In this study,the incorporation of carbon(C) from switchgrass biochar into stable aggregate size fractions was assessed in an Aridisol(from Colorado,USA) dominated by 2:1 clays and an Alfisol(from Virginia,USA) containing weathered mixed 1:1 and 2:1 mineralogy,to evaluate the effect of biochar addition on soil characteristics.The biochar was applied at 4 levels,0,25,50,and 100 g kg~(-1),to the soils grown with wheat in a growth chamber experiment.The changes in soil strength and water-holding capacity using water release curves were measured.In the Colorado soil,the proportion of soil occurring in large aggregates decreased,with concomitant increases in small size fractions.No changes in aggregate size fractions occurred in the Virginia soil.In the Colorado soil,C content increased from 3.3 to 16.8 g kg~(-1),whereas in the53 μm fraction C content increased from 5.7 to 22.6 g kg~(-1) with 100 g kg~(-1)biochar addition.In the Virginia soil,C content within aggregate size fractions increased for each size fraction,except the2 000 μm fraction.The greatest increase(from 6.2 to 22.0 g kg~(-1)) occurred in the 53–250 μm fraction.The results indicated that C was incorporated into larger aggregates in the Virginia soil,but remained largely unassociated to soil particles in the Colorado soil.Biochar addition had no significant effect on water-holding capacity or strength measurements.Adding biochar to more weathered soils with high native soil organic content may result in greater stabilization of incorporated C and result in less loss because of erosion and transport,compared with the soils dominated by 2:1 clays and low native soil organic content.  相似文献   

9.
Mineral Composition and Weathering of Soils Derived from Xiashu Loess   总被引：1，自引：0，他引：1  
Mineralogical, physical and chemical analyses of the soils derived from Xiashu loess were carried out. The primary minerals of these soils were found to be mainly composed of light minerals, such as quartz, feldspar and mica, with traces of heavy minerals. Clay minerals, more complicate in composition, were dominated by hydromica, accompanied by smectite, vermiculite, chlorite, kaolinite, 2:1/1:1 randomly interstratified minerals and small amounts of quartz, goethite, lepidocrocite and hematite, Clay minerals were characterized by low crystallinity and fine particle size. In light of the quartz/feldspars ratio of the 0.01-0.05mm silt fraction, and the clay mineral composition, the freeness of iron oxide, and the silica/sesquioxide and silica/alumina ratios in < 0.002mm clay fraction, it is concluded that the weathering intensity of these soils was lower than those of red soil and yellow earth, but higher than that of brown earth, and that the soil allitization, depotassication and hydroxylation of cl  相似文献   

10.
Soil water-retention characteristics at measurement scales are generally different from those at application scales, and there is scale disparity between them and soil physical properties. The relationships between two water-retention parameters, the scaling parameter related to the inverse of the air-entry pressure (αvG, cm-1) and the curve shape factor related to soil pore-size distribution (n) of the van Genuchten water-retention equation, and soil texture (sand, silt, and clay contents) were examined at multiple scales. One hundred twenty-eight undisturbed soil samples were collected from a 640-m transect located in Fuxin, China. Soil water-retention curves were measured and the van Genuchten parameters were obtained by curve fitting. The relationships between the two parameters and soil texture at the observed scale and at multiple scales were evaluated using Pearson correlation and joint multifractal analyses, respectively. The results of Pearson correlation analysis showed that the parameter αvG was significantly correlated with sand, silt, and clay contents at the observed scale. Joint multifractal analyses, however, indicated that the parameter αvG was not correlated with silt and sand contents at multiple scales. The parameter n was positively correlated with clay content at multiple scales. Sand content was significantly correlated with the parameter n at the observed scale but not at multiple scales. Clay contents were strongly correlated to both water-retention parameters because clay content was relatively low in the soil studied, indicating that water retention was dominated by clay content in the field of this study at all scales. These suggested that multiple-scale analyses were necessary to fully grasp the spatial variability of soil water-retention characteristics.  相似文献   

11.
Abstract

Amorphous and crystalline aluminum and iron oxide minerals play a major role in stabilizing soil structure as measured by aggregate stability and clay dispersion. Aluminum and iron oxide interactions with clays are pH dependent. At low pH, where the oxides carry sufficient positive charge, they precipitate on clay surfaces. These coatings, once formed, are stable at higher pHs. Precipitation of oxides at high pH occurs as phases separate from the clays. Aluminum and iron oxides stabilize clay minerals by decreasing critical coagulation concentration, clay dispersion, water uptake, and clay swelling and by increasing microaggregation. The presence of aluminum and iron oxide minerals in soils has a favorable effect on soil physical properties, increasing aggregate stability, permeability, friability, porosity, and hydraulic conductivity, and reducing swelling, clay dispersion, bulk density, and modulus of rupture.  相似文献   

12.
Adsorption and desorption of salmon sperm DNA on four different colloidal fractions from Brown Soil and clay minerals were studied. The adsorption isotherms of DNA on the examined soil colloids and minerals conformed to the Langmuir equation. The amount of DNA adsorbed followed the order: montmorillonite?fine inorganic clay>fine organic clay>kaolinite>coarse inorganic clay>coarse organic clay. A marked decrease in the adsorption of DNA on organic clays and montmorillonite was observed with the increase of pH from 2.0 to 5.0. Negligible DNA was adsorbed by organic clays above pH 5.0. As for inorganic clays and kaolinite, a slow decrease in DNA adsorption was found with increasing pH from 2.0 to 9.0. The results implied that electrostatic interactions played a more important role in DNA adsorption on organic clays and montmorillonite. Magnesium ion was more efficient than sodium ion in promoting DNA adsorption on soil colloids and minerals. DNA molecules on soil colloids and minerals were desorbed by sequential washing with 10 mM Tris, 100 mM NaCl and 100 mM phosphate at pH 7.0. A percentage of 53.7-64.4% of adsorbed DNA on organic clays and montmorillonite was released, while only 10.7-15.2% of DNA on inorganic clays and kaolinite was desorbed by Tris and NaCl. The percent desorption of DNA from inorganic clays, organic clays, montmorillonite and kaolinite by phosphate was 39.7-42.2, 23.6-28.8, 29.7 and 11.4%, respectively. Data from this work indicated that fine clays dominate the amount of DNA adsorption and coarse clays play a more important role in the binding affinity of DNA in soil. Organic matter may not favor DNA adsorption in permanent-charge soil. The information obtained is of fundamental significance for the understanding of the ultimate fate of extracellular DNA in soil.  相似文献   

13.
胡敏酸对土壤和矿物粘粒分散的影响   总被引：7，自引：0，他引：7       下载免费PDF全文
研究了土壤胡敏酸(Humic acid)对红壤和黄棕壤以及高岭矿和蒙脱矿粘粒分散的影响。研究结果表明：土壤HA对Na+饱和的土壤及矿物粘粒分散作用很大。用H2O2除去土壤有机质后,粘粒分散明显下降。然而,添加少量HA后,又能显著地提高粘粒的分散性。这种现象在两种土壤中,红壤表现更为突出。Na+饱和的高岭矿粘粒分散性很差,而蒙脱矿粘粒分散性很强,这与它们所带电荷量有关。但是,添加少量HA后,高岭矿粘粒分散性急剧提高,而蒙脱矿的变化却很小。试验结果进一步表明：有机质HA对土壤和矿物粘粒分散作用受矿物类型的影响。  相似文献   

14.
Dispersion is an important issue for clay leaching in soils. In paddy soils of the Red River Delta (RRD), flooding with fresh water and relatively high leaching rates can accelerate dispersion and the translocation of clay. For the clay fraction of the puddled horizon of a typical paddy soil of the RRD, the effect of various cations and anions as well as humic acid (HA) at different pH values on the surface charge (SC) were quantified and the dispersion properties were determined in test tubes and described by the C50 value. In the <2 µm fraction, dominated by illite, the proportion of 2:1 vs. 1:1 clay minerals is 5:1. The organic‐C content of the clay fraction is 2.2%. Surface charge was found to be highly pH‐dependent. At pH 8 values of –32 and at pH 1 of –8 mmolc kg–1 were obtained. Complete dispersion was observed at pH > 4, where SC is > –18 mmolc kg–1. The flocculation efficiency of Ca strongly depends on the pH. At pH 4, the C50 value is 0.33, 0.66 at pH 5, and 0.90 mmol L–1 at pH 6. At pH 6, close to realistic conditions of paddy soils, the effect of divalent cations on the SC and flocculation decreases in the order: Pb > Cu > Cd > FeII > Zn > Ca > MnII > Mg; FeII was found to have a slightly stronger effect on flocculation than Ca. An increase in concentrations of Ca, MnII, and Mg from 0 to 1 mmol L–1 resulted in a change in SC from –25 to approx. –15 mmolc kg–1. In comparison, the divalent heavy‐metal cations Pb, Cu, Cd, and Zn were found to neutralize the SC more effectively. At a Pb concentration of 1 mmol L–1, the SC is –2 mmolc kg–1. From pH 3 to 5, the dispersion of the clay fraction is facilitated rather by SO than by Cl–, which can be explained by the higher affinity of SO to the positively charged sites. With an increase of the amount of HA added, the SC continuously shifts to more negative values, and higher concentrations of cations are needed for flocculation. At pH 3, where flocculation is usually observed, the presence of HA at a concentration of 40 mg L–1 resulted in a dispersion of the clay fraction. While high anion concentrations and the presence of HA counteract flocculation by making the SC more negative, FeII and Ca (C50 at pH 6 = 0.8 and 0.9 mmol L–1, respectively) are the main factors for the flocculation of the clay fraction. For FeII and Ca, the most common cations in soil solution, the C50 values were found to be relatively close together at pH 4, 5, and 6, respectively. Depending on the specific mineralogical composition of the clay fraction, SC is a suitable measure for the determination of dispersion properties and for the development of methods to keep clay particles in the soil in the flocculated state.  相似文献   

15.
The effect of changing pH and electrolyte concentration on the dispersion and zeta potential of Na-and Ca-forms of kaolinite, illite and smectite was investigated in relation to changes in their net negative charge. The percentage of dispersible Na-clay and the percentage increase in net negative charge was positively correlated with pH, but the slopes varied from clay to clay. In general, the net negative charge was the primary factor in clay dispersion, and the pH affected clay dispersion by changing the net charge on clay particles. Na-smectite had larger net charge at all pHs than Na-illite and Na-kaolinite, and it always had larger flocculation values. The role of electrolyte concentration could be due to its effect both on flocculation and variable charge component of the clay minerals. The zeta potential at different pHs also reflected the same trend of clay dispersion with net particle charge. In Ca-clays the trends were similar to Na-clays up to pH 7.0. In more alkaline solution CaCO3 formation led to charge reduction on clay particles, resulting in flocculation and reduction of zeta potential. At similar pHs the electrophoretic mobilities of all the clays showed constant potential behaviour. However, the zeta potentials of Ca-clays were always smaller than those of sodic clays because the clays were more aggregated. Net particle charge was the most important factor in controlling clay dispersion for the whole range of pH and ionic strength and for all types of cations.  相似文献   

16.
Soil aggregation and organic matter (OM) conservation are important in the prevention of land degradation. Aggregation processes and OM turnover influence each other and depend on the characteristics of both minerals and organic pools. We assessed the relative importance of the organic and mineral phases at the macroaggregate and colloidal scale in two soils (CHL and SRP, chlorite and serpentine‐rich, respectively) where Mg‐silicates dominated, by incubating them with a relatively degraded and oxidized organic fraction, that is the humic acids (HAs) extracted from the organic horizons of both CHL and SRP. The HA from SRP were more aromatic and richer in phenolic groups, whereas HA from CHL were N‐richer, more aliphatic and richer in carboxyl groups. The SRP soil formed larger amounts of macroaggregates, more stable than in CHL. At the colloidal scale, SRP was more flocculated and clay had a lower electrophoretic mobility than CHL. HA enhanced aggregate formation in both samples but improved aggregate stability only in CHL. In CHL, slight differences in electrophoretic mobility were visible, while in SRP, differences were more pronounced, with a point of zero charge at lower pH and larger hydrodynamic diameter. The abundance of Mg in SRP may have favoured the formation of weaker outer‐sphere interactions and the release of clay‐HA associations upon water dispersion, while in CHL Ca formed more stable bonds with HA. In SRP, ligand exchange reactions can be ruled out, conversely to the dominant bonding mechanism occurring in Al‐silicate dominated soils, with important consequences on the release of OM‐loaded clay particles. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

17.
The adsorption and binding of plasmid p34S DNA on four different colloidal fractions from a Brown soil and clay minerals in the presence of various Ca2+ concentrations, the ability of bound DNA to transform competent cells of CaCl2-treated Escherichia coli, and the resistance of bound DNA to degradation by DNase I were studied. DNA adsorption on soil colloids and clay minerals was promoted in the presence of Ca2+. Kaolinite exhibited the highest adsorption affinity for DNA among the examined soil colloids and clay minerals. In comparison with organo-mineral complexes (organic clays) and fine clays (<0.2 μm), DNA was tightly adsorbed by H2O2-treated clays (inorganic clays) and coarse clays (0.2-2 μm). The transformation efficiency of bound DNA increased with increasing concentrations of Ca2+ at which soil colloid or clay mineral-DNA complexes were formed. DNA bound by kaolinite showed the lowest transformation efficiency, and especially no transformants were observed with kaolinite-DNA complex prepared at 5-100 mM Ca2+. Compared to organic clays and fine clays, DNA bound on inorganic clays and coarse clays showed a lower capacity to transform E. coli at different Ca2+ concentrations. The presence of soil colloids and minerals provided protection to DNA against degradation by DNase I. Montmorillonite, organic clays and fine clays showed stronger protective effects for DNA than inorganic clays and coarse clays. The protection mechanisms as well as the differences in transforming efficiency of plasmid DNA molecules bound on various soil colloidal particles are discussed. The information obtained in this study is of fundamental significance for the understanding of the horizontal dissemination of recombinant DNA and the fate of extracellular DNA in soil environments.  相似文献   

18.
The relationship between the charge characteristics and the dispersibility of soils from reclaimed land (highly dispersive) and adjacent forest area (physically stable) was investigated.

To evaluate the amount of soil charges quantitatively, the measurement based on cation and anion adsorption (ion adsorption method) was attempted in two ways, where special attention was paid to the solution concentration. In the conventional ion adsorption method, the treatments with concentrated solutions (1 mol L-1) were included in the process. In the modified method, soils were treated with dilute solutions (5 mmol L-1), in taking account of the soil solution concentration in humid temperate regions. The amount of charges derived from the modified method was smaller than that from the conventional one, especially in the high pH zone. In a preliminary experiment, the extraction of polyvalent cations from soils was found to be significantly affected by the salt concentration. Thus, the use of solutions with an excessively high concentration was considered to result in an error in the estimation of the active charges in soils which would contribute to the dispersion behavior in the field.

The applicability of the modified method for analyzing the dispersion behavior of soils was evaluated by relating the dispersibility of silts and clays at different pHs with the charge characteristics determined under the same ionic strength. The dispersion ratio of silts of the reclaimed land reached maximum values at pH 5.5, above which the ratio decreased, whereas the ratio of clays began to increase in the pH range above 6. The dispersion ratio of silts of the forest area increased in the pH range above 6, whereas that of clays remained constant at a low level in all the pH ranges below 7. The changes in the dispersibility of silt plus clay fractions corresponded to total charge characteristics determined by the modified method. Thus, the evaluation of soil charges by the modified ion adsorption method was considered to be effective to predict soil dispersibility under field conditions, indicating that it could replace electrokinetic analyses such as electrophoresis in studies on the dispersion/flocculation behavior of soils.  相似文献   

19.
For bacterial inoculants to be effective in soil remediation, the bacterial strain must be capable of overcoming any negative effects of soil minerals on cellular processes. One class of minerals commonly encountered by soil bacteria is clays. Thus, the effect of commonly occurring clay minerals in soils on starvation, survival and 2-hydroxypyridine catabolism by Arthrobacter crystallopoietes was evaluated. Stationary phase A. crystallopoietes cells were suspended in 0.03M, pH7.0, phosphate buffer containing no clay or amended with 0.2% (wt/vol) montmorillonite, sodium montmorillonite or kaolinite. Marked effects of clay minerals on both survival rates and catabolic rates of 2-hydroxypyridine were noted. For example, after 14 weeks starvation, 4.6% of the initial cell population was viable with no clay present, compared to 0.8% (montmorillonite), 22.1% (kaolinite) and 54.1% (sodium montmorillonite) in the presence of the clay minerals. Acclimated and nonacclimated cell populations were used to evaluate 2-hydroxypyridine catabolism. Induction of 2-hydroxypyridine metabolism occurred in the unacclimated cells following starvation. Differential impact of the clay minerals on unacclimated cells was detected. Montmorillonite enhanced the capacity for induction of 2-hydroxypyridine catabolism and its decomposition rate after 0–3 days starvation. For acclimated cells, clay did not affect the metabolic activity prior to starvation, but the presence of clay resulted in increased activity during starvation. For example, after 3 days starvation, a nearly two fold increase in metabolism was detected in the presence of clay minerals. These data suggest that some clay minerals in soil alter the survival time and metabolic activity of soil-amended bacteria, thereby affecting the potential for bioremediation success. Received: 1 March 1996  相似文献   

20.
The sorption of metal ions (Pb2+, Zn2+ and Cu2+) and soil humic acids (HA) from aqueous solutions onto mineral particles (sand, calcite and clay) was investigated using a batch equilibrium system. The sorption reactions in two- component systems (heavy metals-mineral particles and humic acids- mineral particles), as well as interactions in three-component system (heavy metals-humic acids-mineral particles) were examined. Results showed that the presence of humic acids, dissolved or bound onto mineral surfaces, considerably influenced the fixation of heavy metals. The various effects, depending on mineral type, humic concentration and specific metal-ion, were observed in three- component system. Sorption of Cu2+-ions on all minerals studied rapidly increased as the concentration of dissolved HA increased. The amount of Pb2+-ions sorbed on sand slightly decreased, while on kaolin increased between 15 and 20%. Sorption of Zn2+-ions on all minerals studied decreased at pH 4. At pH 5.5 the sorption of Zn2+-ions onto calcite decreased, while on kaolin and sand increased as a function of the humic acid concentration giving the curve with maximum at c(HA) = 2.5 mmol C L-1. At pH 6.5 sorption onto kaolin and sand increased. This effect occurs as a result of the conditional stability constant of Zn-HA complexes increasing at higher pH which in turn promotes the chelation of Zn2+-ions to mineral- bound humic substances. The enhanced sorption of metal ions from the aqueous phase in three-component systems is not only the result of mineral sorption of free metals but also the result of chelation with HA sorbed on the mineral surface.  相似文献   

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