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1.
Aluminium speciation and pH of an acid soil in the presence of fluoride   总被引：2，自引：0，他引：2  
The aim was to determine whether the addition of F to an acid soil reduces the concentration of free Al3+ and other forms that have been shown to be toxic to plants. The ability of two different extracts to reflect Al speciation in the soil solution was also investigated. Addition of F (0-5.2μmolg−1) to an acid soil (pH 4.15, soil solution) increased the pH and total concentrations of Al and F in the soil solution whereas Al3+ remained constant or decreased. Soil solution pH, total soluble Al and Al extracted by 0.01 m CaCl2 are not good predictors of the likelihood of aluminium toxicity in soils containing soluble fluoride.  相似文献   

2.
The cation composition of solutions and leachates from small-diameter laboratory soil columns was examined over a 23-week period after the addition of lime (0, 3 and 6 t ha–1) and/or nitrogen fertilizer (0 or 200 kg N ha–1) to an acid soil (pH 4.2). Water was applied at regular intervals to the surface of the columns and 17 leachate samples collected. Initially, the pH of the leachate was high (6.6) in all treatments (including those without lime) but fell rapidly to approach a steady value of 3.8. Large losses of calcium occurred from all columns; the total equivalent amounts of lime lost ranged from 0.88 (no addition) to 2.38 (with added lime) t CaCO3 ha–1 High concentrations of aluminium (181–325 μM) were present in leachates from all treatments; the addition of 200 kg N ha–1 increased the leaching of Al by 94%; addition of lime also increased the amounts of Al leached (by 52%).
The pH of the soil solution (separated by centrifugation) was influenced by treatment, especially in the top 0–40 mm of the column. Aluminium concentration was related to pH, but the form of the relationship differed amongst the treatments.  相似文献   

3.
Potassium transport was investigated in the root elongation zone of Arabidopsis seedlings during the first minutes of Al3+ exposure, using the non-invasive MIFE microelectrode technique. To prevent pH changes during Al3+ application, and to separate aluminium from acidic stress, plants were pre-treated with 5 mM homoPIPES before addition of AlCl3 (pH 4.2). The 30-min treatment with 50 or 500 μM AlCl3 led to a significant increase in K+ efflux in solutions containing 100 μM CaCl2. This efflux was suppressed by high concentrations of Ca2+ (10 mM) in the bathing solution. Our results suggest that elevated external Ca2+ activities can sustain K+ influx in the root elongation zone during Al3+ exposure either by maintaining [Ca2+]cyt or by affecting Al3+ uptake across the plasma membrane.  相似文献   

4.
Abstract. The behaviour of potassium (K) in a range of arable soils was examined by plotting the change in exchangeable K of the topsoil (Δ Kex) at the end of a 3–5 year period against the K balance over the same period (fertilizer K applied minus offtake in crops, estimated from farmers' records of yield and straw removal). Based on the assumption that values for offtake per tonne of crop yield used for UK arable crops MAFF 2000) are valid averages, 10–50% of Δ Kex was explained by the balance, relationships being stronger on shallow/stony soils. Excess fertilizer tended to increase Kex and reduced fertilization decreased it, requiring between 1.2 and 5.4 kg K ha−1 for each mg L−1Δ Kex. However, merely to prevent Kex falling required an extra 20 kg K ha−1 yr−1 fertilizer on Chalk soils and soils formed in the overlying Tertiary and Quaternary deposits, despite clay contents >18%. Whereas, on older geological materials, medium soils needed no extra K and clays gained 17 kg K ha−1 yr−1. It is unlikely that the apparent losses on some soil types are anomalies due to greater crop K contents. Theory and the literature suggest leaching from the topsoil as a major factor; accumulation in the subsoil was not measured. Recommendations for K fertilization of UK soils might be improved by including loss or gain corrections for certain soil types.  相似文献   

5.
A standardized dataset of derived soil properties for the 106 soil units considered on FAO-UNESCO's 1:5 million scale Soil Map of the World is presented. It was derived from a statistical analysis of the 4353 soil profiles held in the WISE (World Inventory of Soil Emission) database, which was developed at the International Soil Reference and Information Centre (ISRIC) for the geographic quantification of soil factors that control processes of global change. Median values are presented by soil unit for selected soil properties including: pH(H2O); organic carbon content; cation exchange capacity; sum of exchangeable Ca2+, Mg2+ and K+; exchangeable sodium percentage; bulk density; total porosity; available water capacity; soil drainage class; and gravel content class. Medians for these variables are presented both for the topsoil (0–30 cm) and subsoil (30–100 cm), where applicable. The data set can help to refine ratings for soil quality in global environmental models pending the availability of comprehensive georeferenced databases on soil and terrain resources such as SOTER, the World Soil and Terrain Database. In a Geographical Information System (GIS) it can be linked to the units shown on the digital Soil Map of the World through the legend code.  相似文献   

6.
Surface and subsurface samples of three tropical soils were examined with respect to their interaction with dilute solutions of sulphuric acid of pH 3. In calcareous clayey samples with a large cation exchange capacity the H+ was replaced by an equivalent concentration of metal cations which remained in solution along with SO2-4 as counterion. In a coarse-textured neutral soil with small cation exchange capacity, there was less chemical interaction and a major proportion of the H2SO4 remained unchanged in the equilibrium solution. Another soil exhibited considerable ability to remove SO2-4 from solution and, therefore, the total ionic concentration was greatly reduced. Other samples showed behaviour which was intermediate to these three types.
The ability to adsorb SO2-4 is one of the most important factors which determines the nature of the interaction of soil with dilute sulphuric acid. This ability was shown to be affected by the content of hydrous sesquioxides and organic matter in these soils.  相似文献   

7.
A plot with a high aluminum (Al) concentration in soil solution was found in Kumagaya, central Japan; the maximum was 4.0 mg L−1 as total dissolved Al (TD-Al) at a depth of 10 cm in August 2000. The soil type was Dystric Andosols with three horizons, A/Bw1/Bw2, which contained a considerable quantity of Al extracted by dithionite-citrate and acid-oxalate extractants. The upper two horizons were acidic with soil pH (H2O) of 4.4 and 4.6. The fundamental cause of the high TD-Al concentration was the low pH with a very low base saturation of less than 2%. The seasonal change in TD-Al concentrations in soil solution at a depth of 10 cm was significantly and positively correlated with the nitrate concentrations but weakly and rather negatively correlated with the sulfate concentrations. Nitrification functioned as the direct acid source to cause the TD-Al concentrations to fluctuate strongly, whereas sulfate adsorption onto the soil at the research plot functioned as a sink of proton.  相似文献   

8.
The reactions of two organic (citrate and fulvate) and two inorganic (chloride and phosphogypsum) calcium compounds were studied during leaching of columns of unsaturated acidic soil. The potential of these compounds to decrease the aluminium concentration in the soil solution and remove exchangeable aluminium, and their effects on soil acidity are described. The calcium citrate solution increased the soil solution pH from 5 to a maximum value of 7 in the upper portion of the column. In contrast, the fulvate, calcium chloride and phosphogypsum solutions had little effect on soil-solution pH. Treatment with calcium citrate, or fulvate solution that contained 51 mm Na, removed most of the exchangeable aluminium from the column. The cation exchange sites in the upper portion of the column were saturated with calcium, and the cation exchange capacity of the soil was increased from 35 to c. 80 mmolc kg?1 in the calcium citrate treatment. Leachate from this treatment contained low (< 2 mm ) calcium concentrations and high aluminium concentrations. In contrast, the above changes were not shown by the calcium chloride and phosphogypsum treatments. In these treatments the calcium concentration in the leachate was equal to that in the inflowing solution, which indicated that calcium was transported through the entire column. These results suggest that calcium alone was ineffective in displacing aluminium from the cation exchange sites and a strong complexing agent such as citrate or fulvate is needed to mobilize the exchangeable aluminium.  相似文献   

9.
Abstract. The effect of liming and deep cultivation on soil properties and root development was investigated in two cultivated shallow fen peats resting on acid gyttja (lake mud) soils. Root growth was in general dependent on soil pH and aluminium content of the soil. A soil pH (H2O) below 5 adversely affected roots and a pH below 4 severely restricted root growth. Liming of the topsoil or the subsoil and to some extent deep cultivation improved root growth. Increased rooting depth made it possible for plants to utilize soil water to a greater depth in the profile and to support a larger crop yield.  相似文献   

10.
The effects of lime (applied in the field) on the amounts of total and isotopically-exchange-able phosphate adsorbed from solutions were measured in five soils. The total amount of phosphate adsorbed without lime was in the range 200 to 1700 μg P per g of soil at 0.05 μg P cm−3 of solution. Lime diminished the amount of phosphate adsorbed at all concentrations of solution in an oxisol and a dystropept; in an ultisol and another dystropept, lime tended to increase sorption at small concentrations and diminish it at large concentrations; in a dystrandept that contained spheroidal allophane and a great deal of organic matter, lime increased adsorption at all concentrations up to 1 μg P cm−3. Lime increased the proportion of added phosphate that was isotopically exchangeable in the oxisol and one dystropept, had no effect in the other dystropept, and diminished the proportion in the ultisol and dystrandept.
Adsorbed phosphate was subsequently desorbed by suspending the soils in solutions without phosphate. After desorption the quantity of exchangeable phosphate in all soils was closely correlated with aluminium extracted by ammonium oxalate; buffer power was correlated in all except the dystrandept, in which it was larger per unit of aluminium than in the other soils; possibly the cause was aluminium associated with organic matter. In all soils lime diminished buffer power allowing a specific amount of exchangeable phosphate to maintain a larger concentration in solution. The beneficial effects of lime on exchangeable phosphate after desorption were consistent among soils, despite inconsistent results when the phosphate was adsorbed.  相似文献   

11.
Abstract. Land application of organic wastes can result in the accumulation of available soil phosphorus (P) and in an increase risk of eutrophication of surface and shallow groundwaters. We conducted laboratory experiments to examine the effect of waste application on the concentration of dissolved reactive phosphorus (DRP) in 1:5 soil to 0.005 m CaCl2 suspensions. Ten organic wastes, of which eight were mature composts, were applied to a P-rich Calcaric Fluvisol at rates ranging from 0 to 10% of soil by weight, and the difference in DRP concentration between suspensions containing waste and the untreated control (ΔDRP) was measured over a period of 300 days. In half of the suspensions of each waste–soil combination, 80 mg P (as KH2PO4) kg−1 soil was applied at day 14. Values of ΔDRP were generally positive, but a significant number of negative values were also recorded for some wastes and application rates, particularly at later sampling times if inorganic P had been added. Regression analyses revealed that ΔDRP (i) increased with increasing soluble reactive P at all times and (ii) increased in the short term, but decreased in the long term with increasing water soluble organic carbon in the waste. The fact that ΔDRP was sometimes negative for some waste types suggests that application of organic waste to soil does not necessarily increase eutrophication risks caused by soil P losses.  相似文献   

12.
The effect of pH on the adsorption of copper (Cu), lead (Pb) and cadmium (Cd) by a peat soil was studied, and the results compared with those corresponding to cation binding by a dissolved peat humic acid (HA), and interpreted with a NICA–Donnan model. A potentiometric titration technique was used to determine the adsorption isotherms for H+, at different ionic strengths, and for Cu2+, Pb2+ and Cd2+ at different pH values, in a peat soil. The effect of the ionic strength on proton binding was similar for the soil (solid) organic matter and for dissolved HA. The adsorption isotherms for cation–peat and the binding curves cation–dissolved HA are almost parallel, although more cation was adsorbed per kg of C in the dissolved HA. The effect of pH on cation binding is similar for dissolved organic matter and for the organic soil. At low metal concentration the amount of adsorbed metal followed the order Cu2+ > Pb2+ > Cd2+. The cation-binding parameters obtained with the NICA–Donnan model allow excellent simulation of the effect of pH on the adsorption of Cu, Pb and Cd ions in the studied peat soil. The binding constants for the peat suspension were greater than the corresponding generic parameters for dissolved HA. Speciation calculations showed that for Cu and Pb, the most abundant fraction was the metal adsorbed on peat, whereas for Cd the most abundant fraction was dissolved metal.  相似文献   

13.
We studied the effect of repeated application (once every 2 d) of a fertilizer solution with different ratios of NH4+ - and NO3−-N on N2O emission from soil. After the excess fertilizer solution was drained from soil, the water content of soil was adjusted to 50% of the maximum water-holding capacity by suction at 6 × 103 Pa. Repeated application of NH4+- rich fertilizer solution stimulated nitrification in soil more than NO3−-rich fertilizer. Although the evolution of N2O through nitrifier denitrification tended to increase with the repeated addition of a fertilizer solution rich in NH4+ rather than in NO3−, the contribution of nitrifier denitrification remained at levels of 20 to 36% of the total emission regardless of the inorganic N composition. The total emission of N2O also tended to increase with the application of NH4+- rather than NO3−-rich fertilizer. It was suggested that the coupled process of nitrification and denitrification at micro-aerobic sites became important when fertilizer rich in NH4+ was applied to soil under relatively aerobic conditions.  相似文献   

14.
Abstract. The aim of this study was to investigate the effects of water submergence depth on radial oxygen loss (ROL), soil solution chemistry and rice growth performance in acid sulphate soils in southern Vietnam. ROL was measured in a solution culture. In a separate pot experiment the impact of water submergence depth on rice growth and soil solution chemistry was studied. Three submergence depths were used in the two experiments (5, 10 and 15 cm). ROL declined with submergence depth and was significantly greater in young roots (with no root hairs) than in older roots. In the pot experiment rice growth and soil solution chemistry were clearly affected by the submergence depth. During the first crop at 5 cm submergence, there was a significantly higher yield and a higher oxidation state (pe+pH) compared to 10 or 15 cm submergence. The Fe concentration was significantly greater at the 5 cm depth compared to the 10 or 15 cm depth. SO42– reduction was delayed at the 5 cm depth. Rice yield was c. 25% less at the 15 cm than at the 5 cm depth. During a second crop, there was a substantial SO42- reduction and H2S formation and almost no significant effects of submergence depth on either soil solution chemistry or crop yield. In a field experiment with a dry-season rice crop, yield and Fe, Al and SO42– concentrations were higher at a shallow submergence depth than at greater depths in the same field, showing similar depth trends to those found during the first crop in the pot experiment. Farmers should be advised to use a shallow submergence depth and, if possible, avoid deep-rooted rice varieties. A conceptual model is suggested, which summarizes the relationships between ROL and soil solution chemistry.  相似文献   

15.
Abstract. Lime was applied in summer 1981 at rates up to 201 ha−1 prior to reseeding an unimproved peaty hill soil. A marked pH gradient with depth developed showing that 3 years after application lime had very little effect below a depth of 5 cm. Soil pH values for 0–7.5 cm samples were: nil lime-4.2; 1 t ha−1-pH 4.3; 2 tha−1-pH 4.6; 4 t ha−1-pH 5.0; 6 t ha−1-pH 5.6. In the 0–2.5 cm layer pH values were much higher.
In all years at least 80% of maximum yield was achieved from an initial application of 21 ha−1 lime. Botanical analysis showed that maximum persistence of sown species, perennial ryegrass and timothy, occurred from 2 t ha−1 lime; 6 t ha−1 lime was necessary for maximum persistence of clover. Lime application had only small effects on the mineral composition of the herbage.  相似文献   

16.
Amelioration of a highly alkaline soil by trees in northern India   总被引：2，自引：0，他引：2  
Abstract. A study was carried out to compare the impact of 6-year-old plantations of Prosopis juliflora (Swartz) D.C., Dalbergia sissoo Roxb. Ex. D.C. and Eucalyptus tereticornis Sm. on the physical and chemical properties of sodic soil in the Indo-Gangetic alluvial plains of Uttar Pradesh, India. Soil properties under the three tree species showed significant improvement through a reduction in the pH, electrical conductivity, exchangeable sodium percentage, CaCO3 and gypsum requirement, and by increase in organic C, total N, and available P and K. The six years of reclamation had achieved a marked reduction in exchangeable sodium (from 11.5 to 4.5 cmolc kg−1) to a depth of 1.5 m in the soil profile, whereas the levels of exchangeable calcium, magnesium and potassium had increased. There was also a significant reduction in soil bulk density (from 1.66 to 1.24 g cm−3) and increases in porosity, water holding capacity, field capacity, permeability and infiltration rate. The equilibrium infiltration rate after 455 min increased from 0.03 cm h−1 in the control to 0.13 cm h−1 under P juliflora and D. sissoo and 0.10 cm h−1 under E. tereticornis . It is concluded that salt-tolerant tree species have a significant impact on soil properties, which could help to rehabilitate the sodic wastelands in the region.  相似文献   

17.
The retention walls in a pond containing the residues from the pyrite mine of Aznalcóllar (southern Spain) broke open on 25 April 1998, spilling approximately 6 × 106 m3 of polluted water and toxic tailings, which affected some 55 km2. Drying and aeration of the tailings resulted in oxidation, forming an acidic solution with high pollutant contents, the effects of which were studied in a calcareous soil. The infiltration of this solution markedly affected only the first 12 mm of the soil, where strong acidification caused the weathering of the carbonates, and where the fine mineral particles were hydrolysed. The SO42− ions in the acidic solution precipitated almost entirely at this depth, forming gypsum, hydroxysulphates and complex sulphates. The Fe3+ ions also precipitated there, mainly in amorphous or poorly crystallized forms, adsorbing to As, Sb, Tl and Pb dissolved in the acidic solution. The Al3+ ions, though partly precipitating in the acidic layer, accumulated mostly where the soil pH exceeded 5.5 (12–14 mm in depth). They did so primarily as amorphous or poorly crystallized forms, adsorbing to Cu dissolved in the acidic solution. The Zn2+ and Cd2+ ions accumulated mainly at pH > 7.0 (19–21 mm in depth), being adsorbed chiefly by clay mineral. After 15 months, only the first 20 mm of the soil were acidified by the oxidation of the tailings and most of the pollutants did not penetrate deeper than 100 mm. Consequently, the speed of the cleanup of the toxic spill is not as important as a thorough removal of tailings together with the upper 10 cm of the soil.  相似文献   

18.
Abstract. Eight lysimeters, each with a surface area of 0.5 m2 and a length of 60 cm, were taken over mole drains from a Denchworth soil and divided into two groups with either a standard agricultural tilth or a finer, deeper topsoil tilth. They were variously instrumented to measure soil moisture content at three depths and losses of nitrate, a bromide tracer and radiolabelled isoproturon, all of which were followed over a year. Leaching of isoproturon was initiated by artificial irrigation either 1 or 39 days after application. The finer tilth seemed to increase the water-holding capacity of the topsoil, and this resulted in slower wetting of the subsoil, decreased flow volumes from the first events of the season and a delay of approximately four weeks in the time to the maximum concentration of the bromide tracer in leachate. The finer topsoil tilth also decreased maximum concentrations of isoproturon from 29 to 15 μg l−1 following irrigation 1 day after treatment and from 43 to 9 μg l−1 following irrigation 39 days after treatment. Total losses of isoproturon were three times larger with the standard agricultural tilth. Differences were attributed to a decrease in bypass flow through the topsoil with the finer tilth, particularly during events early in the season. There was a small decrease in total losses of nitrate in leachate from the finer tilth compared to that from the standard tilth.  相似文献   

19.
The numerical density, Nv , of the pore structure of soil is the number of disjoint networks of pores per unit volume of soil. A method is described for estimating Nv of patterns of cracks that dominate in many clay subsoils. The cracks are photographed from numerous close-spaced parallel sections and skeletonized; by comparing the skeletonized photographs sequentially, individual networks are tracked from one section to another and counted. The average number of networks that appears or disappears per section in the sequence is a measure of the numerical density and is obtained by regressing the counts on the volume of soil spanned by the sections. The regressions for appearances and disappearances converge on one another and stabilize within 10 to 20 sections, so that Nv can be estimated for a sample of soil with moderate effort.
Estimates of Nv for cracks wider than 60 μm in subsoil of the Windsor series, sampled at two nearby sites and 5 years apart in time and determined from sections at 50 μm intervals, were approximately 32 cm−3 and 36cm−3. That of Nv in the Swanwick series subsoil nearby was about 75 cm−3.  相似文献   

20.
Abstract. Soil samples from a 32-year grassland field experiment were taken from 0–5, 5–10, and 10–15 cm soil depths in February 2002. Plots received annual treatments of unamended control, mineral fertilizer, three rates of pig slurry and three rates of cow slurry, each with six replicates. Samples were analysed for cation exchange capacity (CEC), exchangeable cations (Na+, K+, Ca2+, Mg2+), pH and Olsen P. Exchangeable sodium percentage (ESP) was calculated as a sodicity indicator. Mean ESP was generally greater for slurry treatments than the control, with a trend of increasing ESP with application rate. This was particularly marked for cow slurry. At 0–5 cm depth ESP increased from 1.18 in the control to 1.75 at the highest rate of pig slurry and 5.60 at the highest rate of cow slurry. Similar trends were shown for CEC, exchangeable Na+, K+ and Mg2+, Ca2+ and Olsen P. The build-up of soil P due to slurry applications, together with this combination of physical and chemical factors, may increase the risk of P loss to surface waters, particularly from soils receiving high rates of cow slurry.  相似文献   

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