Fractionation of organo-mineral complexes by sedimentation and density techniques

Soil samples were fractionated by sedimentation in water and by flotation in heavy liquids to separate complexed and uncomplexed organic and inorganic components. Flocculation of clays in heavy organic liquids was delayed by addition of a surfactant. Heavy liquids and surfactants sorbed by soil components were removed by washing with acetone-water mixtures.In a sample of a red-brown earth, the organic carbon and nitrogen contents were highest in the finest separates. In samples of a ground-water rendzina and a chernozemic soil, the coarse clay and silt separates had the highest organic carbon and nitrogen contents. Organic matter was concentrated in low density fractions in all separates. Carbon/nitrogen ratios were lowest in the finer and heavier separates. Calcium, and to a lesser extent manganese, iron and phosphorus, were concentrated in low density fractions: thus these elements appear to be associated with organic matter and may be important in organo-mineral complex formation. Carbonates, titanium, iron, silicon and potassium were concentrated at the highest densities.Organic fractions < 2.06 g cm^?3 from sand size separates were insoluble in alkali and had wide carbon/nitrogen ratios characteristic of plant debris. The light fractions from fine silt and coarse clay separates were more soluble in alkali but showed high ratios of humic to fulvic materials and high absorption at 280 nm. Such materials were considered to be microbial cell debris and were associated with high contents of disordered aluminium and iron oxides and expanding lattice silicates in 1 to 5 μm aggregates.Heavier fractions, particularly of finer clay separates, contained more fulvic and humic materials of a more aliphatic nature than those in < 2.06 g cm^?3 fractions. It is suggested that physical sorption on clay surfaces may be more important in these fractions. Ellite and kaolinite were concentrated in medium density fractions, and contents of some iron oxides and titanium minerals were highest in fractions > 2.06 g cm^?3. Such minerals plus quartz and feldspars were associated with minor amounts of organic matter or possibly were not involved in organo-mineral associations.     

Properties of soil particle size separates after 40 years of continuous corn

Abstract

Changes in chemical and mineralogical characteristics associated with different particle size fractions in soil after 40 years of continuous production of corn by the conventional tillage method (CC) as compared with those of an adjacent native grassland site (NG) are investigated. Results indicate that corn cropping in a soil previously supporting native vegetation produces a decline in total and humified organic matter, phenolic compounds, enzymatic activities, cation exchange capacity (CEC), and hydrosoluble ions, both in the whole soil and in its particle‐size separates. The’ largest losses in organic carbon (C) and nitrogen (N) contents of the cultivated soil were observed in the sandy fractions, the lowest in the silt+clay separates. The humification index (HI) indicates a higher degree of humification of the organic matter in NG than in CC samples. For both NG and CC sites the finest fraction (silt+clay) resulted to be enriched in organic C, total N, humus, phenolic compounds, enzyme activity, CEC, and hydrosoluble ions with the only exception of mineral N forms and sulphates (SO₄). Slight differences were observed in the mineralogical composition of NG and CC soils. The sandy fractions of NG showed greater amounts of phyllosilicates while a lower content was found in the silt+clay fraction of CC as a consequence of a crumbling of parent rock into small pieces induced by repeated tillage practices.     

Estimation of soil texture from permanent wilting point measured with a chilled‐mirror dewpoint technique

Soil texture is an important factor governing a range of physical properties and processes in soil. The clay and fine fractions of soil are particularly important in controlling soil water retention, hydraulic properties, water flow and transport. Modern soil texture analysis techniques (x‐ray attenuation, laser diffraction and particle counting) are very laborious with expensive instrumentation. Chilled‐mirror dewpoint potentiameters allows for the rapid measurement of the permanent wilting point (PWP) of soil. As the PWP is strongly dictated by soil texture, we tested the applicability of PWP measured by a dewpoint potentiameter in predicting the clay, silt and sand content of humid tropical soils. The clay, silt, and sand content, organic matter and PWP were determined for 21 soils. Three regression models were developed to estimate the fine fractions and validated using independent soil data. While the first model showed reasonable accuracy (RMSE 16.4%; MAE 13.5%) in estimating the clay, incorporating the organic matter into the equation improved the predictions of the second model (RMSE 17.3%; MAE 10.9%). When used on all soil data, the accuracy of the third model in predicting the fine fraction was poor (RMSE 31.9%; MAE 24.5%). However, for soils with silt content greater than 30%, the model prediction was quite accurate (RMSE 7–12%; MAE 7–9%). The models were used to estimate the sand content and soil textures of soils, which proved relatively accurate. The dewpoint potentiometer can serve a dual purpose of rapidly estimating the PWP and the clay, fine fraction, and soil texture of soils in a cost efficient way.     

Straw incorporation and soil organic matter in macro-aggregates and particle size separates

Two field experiments in which straw has been removed or incorporated for 17 yr (loamy sand) and 10 yr (sandy clay loam) were sampled to examine the effect of straw on the C and N contents in whole soil samples, macro-aggregate fractions and primary particle-size separates. The particle size composition of the aggregate fractions was determined. Aggregates were isolated by dry sieving. Straw incorporation increased the number of 1–20 mm aggregates in the loamy sand but no effect was noted in the sandy clay loam. Straw had no effect on the particle size composition of the various aggregate fractions. After correction for loose sand that accumulated in the aggregate fractions during dry sieving, macro-aggregates appeared to be enriched in clay and silt compared with whole soil samples. Because of the possible detachment of sand particles from the exterior surface of aggregates during sieving operations, it was inferred that the particle size composition of macro-aggregates is similar to that of the bulk soil. The organic matter contents of the aggregate fractions were closely correlated with their clay + silt contents. Differences in the organic matter content of clay isolated from whole soil samples and aggregate fractions were generally small. This was also true for the silt-size separates. In both soils, straw incorporation increased the organic matter content of nearly all clay and silt separates; for silt this was generally twice that observed for clay. The amounts of soil C, derived from straw, left in the loamy sand and sandy clay loam at the time of sampling were 4.4 and 4.5 t ha^?1, corresponding to 12 and 21% of the straw C added. The C/N ratios of the straw-derived soil organic matter were 11 and 12 for the loamy sand and sandy clay loam, respectively.     

Predicting soil water availability from texture and organic matter content for Nigerian soils

Abstract

Twenty soil samples were collected from three different locations in Nigeria to study the relationship between available water, organic matter content and particle size class with the objective to develop a prediction equation for available water capacity using these soil properties. A high correlation between available water and the textural separates of the soil was obtained, the highest correlation being with silt (r = 0.96). Organic matter in these soils did not highly correlate with available water (r = 0.22). Silt was found to contribute most to the total variation in available water (95.5%). However, when clay was introduced in the regression equation, 98% of the variation in available water capacity was accounted for with a smaller standard error (1.31) than when using silt content alone (1.97). The equation: Awc = 0.93 + 0.54 silt + 0.13 clay can be used to predict the available water capacity of these soils.     

Predicting soil water retention characteristics from soil physical and chemical properties

Abstract

Knowledge of soil water availability for plant growth is vital for the development of plant growth simulation models. Data on soil water availability are often not available because field and laboratory measurements of soil water content are time‐consuming and tedious. The objective of this study was to develop alternative procedures to predict water content at ‐10 kPa (UL10), ‐33 kPa (U133), ‐1500 kPa (LL), and the potential available water capacity (AWC) from easily and routinely available soil properties. Multiple regression equations for soil orders of Soil Taxonomy were developed using a database containing information of about 12,000 pedons of the continental U.S., Hawaii, Puerto Rico, and some foreign countries. Regression equations with bulk density, sand, silt, clay, and organic carbon contents accounted for up to 83% of the variation in UL10 for all orders except Ultisols. For Ultisols, sand content accounted for up to 90% of the variation in UL10. Equations with clay and organic carbon contents accounted for up to 75% of the variability in UL33 for all except Aridisols, Oxisols, Vertisols, and Spodosols. For these four orders, equations with bulk density, clay, silt, and sand contents accounted for up to 81% of the variation in UL33. LL was linearly related to clay content. Clay content accounted for up to 91% of the variation in LL for all but Oxisols and Vertisols. More accurate predictions of AWC resulted when AWC was computed from UL10 and LL water content data. Equations with bulk density alone or bulk density plus silt and/or sand contents accounted for up to 83% of the variation in AWC for all except Entisols, Inceptisols, and Spodosols.     

Selenite fixation by soil particle-size separates

The fixation of selenite by clay- (< 2 μm), silt- (2–20 μm) and sand-size (20–2000 μm) separates from two arable soils was examined in solutions of ⁷⁵Se-labelled sodium selenite using a Se/sample ratio of 1/10⁶. Size separates were isolated by ultrasonic dispersion and gravity sedimentation. Selenite fixation was determined after equilibration periods ranging from 5 min to 26 h. Hydrogen peroxide-treated samples were included to examine the effect of organic matter on selenite fixation capacity.
The relative distribution of native Se, C, dithionite/citrate-extractable Fe and Al between size separates was similar. Concentrations in clay were four to nine times higher than in whole soils, silt showing two to five times higher concentrations and sand being very low in Se, C, Fe and Al.
After 1 h, clay, silt and sand fixed 64–65%, 45–61% and <5% of the selenite added, respectively. The fixation on whole soils was 14–18%. After 1 day, fixation on clay, silt, sand and whole soil increased to 78–87%, 67–79%, 3–14% and 31–39%, respectively.
Hydrogen peroxide-treatment reduced the selenite fixation capacity of whole soil, silt and sand to very low levels. Fixation on peroxide-treated clay was in accord with values for pure clay minerals reported in the literature. Generally, the fixation capacity of peroxide-treated natural clay and pure clay minerals was only half that observed for intact clay-size separates, demonstrating the importance of organic matter in soil selenite fixation capacity.     

伊犁河谷不同森林模式下土壤的养分特征和粒径组成

[目的]对伊犁河谷不同森林模式下土壤粒径组成和养分空间特征进行研究,为科学栽培和可持续经营提供理论依据。[方法]通过野外采样与室内试验,分析伊犁河谷不同模式下土壤粒径分布特征及其与土壤理化性质的关系。[结果]7个模式林地土壤基本集中在细粉粒和粗粉粒两个粒级。主要由细粉粒—粗粉粒—黏粒、细粉粒—粗粉粒—极细砂粒和粗粉粒—细粉粒—极细砂粒为主的质地组成,其中细粉粒—粗粉粒—黏粒土壤养分较佳,相比之下含有砂粒的土壤养分较低。土壤有机质和土壤碱解氮与黏粒和细粉粒含量的关系非常密切,尤其是细粉粒;速效磷与砂粒、黏粒和细粉粒呈正相关;速效钾与黏粒和细粉粒含量的关系密切,随着其含量增加而增加,跟砂粒呈显著负相关,砂粒含量高,速效钾含量降低。[结论]伊犁河谷7个模式林分土壤养分状况各异,养分各项指标含量不同,可根据养分状况进行抚育管理。各模式土壤中粉粒含量占绝对优势。根据各养分含量与各粒径组成之间的相关性分析表明,土壤颗粒越细,与土壤养分的关系越密切。     

Distribution of polycyclic aromatic hydrocarbons in particle‐size separates and density fractions of typical agricultural soils in the Yangtze River Delta,east China

Soil organic matter can be divided into different organic carbon (C) pools with different turnover rates. The organic pollutants in soils associated with these organic C pools may have different bioavailability and environmental risks during the decomposition of soil organic matter. We studied the distribution patterns of 15 USEPA priority polycyclic aromatic hydrocarbons (PAHs) in different particle‐size separates (clay, fine silt, coarse silt, fine sand and coarse sand) and density fractions (light and heavy fractions) of nine agricultural topsoils (0–20 cm depth) from a contaminated area in the Yangtze River Delta region of east China. There was a decreasing trend in PAH concentration in particle‐size separates with decreasing particle size. However, the different particle‐size separates had similar PAH composition. The concentration of PAHs in the light fraction ranged from 13 037 to 107 299 μg kg^?1, far higher than in the heavy fraction, which ranged from 222 to 298 μg kg^?1. Although the light fraction accounted for only 0.4–2.3% of the soils, it was associated with 31.5–69.5% of soil PAHs. The organic matter in coarse silt had the strongest capacity for enrichment with PAHs. Combining the distributions of PAHs and the turnover rates of organic matter in different soil fractions, the environmental risks of PAH‐polluted soils may be due mainly to the PAHs associated with sand and the light fraction.     

STUDIES OF SOIL ORGANO-MINERAL FRACTIONS

Sand-, silt-, and clay-size organo-mineral fractions were isolated in bulk from surface horizons of five soils following ultrasonic dispersion in water. Good clay separation was achieved for all except one highly organic, calcareous clay soil. Organic-N and -C were concentrated in the clay and silt fractions but for each soil the organic C : N ratio decreased in the order sand > silt > whole soil > clay. Acid hydrolysis of the silt and clay fractions revealed a slight concentration of amino acid-N and NH₄-N in the clays but only small differences in the distribution of individual amino acids were observed. The results suggest that both silt and clay fractions may be important in the stabilization of soil organic matter.     

Soil particle size range correction for improved calibration relationship between the laser-diffraction method and sieve-pipette method

Particle size fraction(clay, silt, and sand) is an important characteristic that influences several soil functions. The laser-diffraction method(LDM) provides a fast and cost-effective measurement of particle size distribution, but the results usually differ from those obtained by the traditional sieve-pipette method(SPM). This difference can persist even when calibration is applied between the two methods. This partly relates to the different size ranges of particles measured by the two methods as a result of different operational principles, i.e., particle sedimentation according to Stokes’ Law vs. Mie theory for laser beam scattering. The objective of this study was to identify particle size ranges of LDM equivalent to those measured by SPM and evaluate whether new calibration models based on size range correction can be used to improve LDM-estimated particle size fractions, using 51 soil samples with various texture collected from five soil orders in New Zealand. Particle size distribution was determined using both LDM and SPM. Compared with SPM, original data from LDM underestimated the clay fraction(< 2 μm), overestimated the silt fraction(2–53 μm), but provided a good estimation of the sand fraction(53–2 000 μm).Results from three statistical indices, including Pearson’s correlation coefficient, slope, and Lin’s concordance correlation coefficient, showed that the size ranges of < 2 and 2–53 μm defined by SPM corresponded with the < 5 and 5–53 μm size ranges by LDM, respectively. Compared with the traditional calibration(based on the same particle size ranges), new calibration models(based on the corrected size ranges of these two methods) improved the estimation of clay and silt contents by LDM. Compared with soil-specific models(i.e., different models were developed for different soils), a universal model may be more parsimonious for estimating particle size fractions if the samples to be assessed represent multiple soil orders.     

Distribution of DTPA‐extractable Fe,Zn, and cu in soil particle‐size fractions

Abstract

To examine the distribution of DTPA‐extractable Fe, Zn, and Cu in clay, silt, and sand fractions; surface soils were collected from cultivated fields of North Dakota, South Dakota, West Virginia, Iowa, Ohio, and Illinois. Clay, silt, and sand fractions were separated after sonic dispersion of soil water suspension and analyzed for DTPA‐extractable Fe, Zn, and Cu. In general, clay had the highest and sand the lowest amount of DTPA‐extractable metals. Consequently, clay had the highest and sand the lowest intensity and capacity factors for these metals since DTPA micronutrient test measures both these factors.     

Studies of nitrogen immobilization and mineralization in calcareous soils—I: Distribution of immobilized nitrogen amongst soil fractions of different particle size and density

¹⁵NO₃^? was immobilized in a calcareous clay and a calcareous sandy soil during incubation of each soil with glucose and wheat straw. Changes in the distribution of immobilized ¹⁵N amongst soil extracts and soil fractions of different particle size and density were determined during periods of net N immobilization.The nature of the organic-C amendment, but not soil type, significantly influenced both the distribution of the immobilized ¹⁵N and the pattern of changes of the organic-¹⁵N of soil fractions with time. In straw-amended soils, approx. 20% of the organic-¹⁵N became associated with a light fraction, sp. gr. < 1.59, the remainder becoming distributed mainly amongst the silt and clay fractions. In glucoseamended soils, very little (< 1.2%) of the ¹⁵N was immobilized in the light fraction, sp. gr. < 1.59, most being rapidly distributed amongst the silt and clay fractions. During a period of complete immobilization, organic-¹⁵N was transferred from the fine clay to the silt and coarse clay fractions.Silt, coarse clay and fine clay components from glucose-amended soils sampled at the end of the net immobilization phase were further fractionated densimetrically into light (sp. gr. < 2.06) and heavy (sp. gr. > 2.06) subfractions. The organic-¹⁵N of respective light subfractions accounted for 43–64% of the total organic-¹⁵N of the silt, 1–9% of that of the coarse clay and 19–21% of that of the fine clay fractions.     

A routine method to study soil organic matter by particle‐size fractionation: Examples for tropical soils

Abstract

Particle size fractionation is becoming commonly used for studying soil organic matter (OM). However, isolation of clay and silt represents a long and thus tedious step in the fractionation procedure. We propose an approach identical to the one utilized in particle size analysis with an estimation of the recoveries from aliquots ("aliquot”; method) of the 0–2 and 0–20 μm fractions and no entire isolation ("decanting”; method) of clay and silt. In comparison with the “decanting”; method, the fraction and carbon (C) recoveries obtained by the “aliquot”; method were satisfactory, but those of nitrogen (N) being hardly interpretable because of an insufficient accuracy of the determination method. The recommended method saves time and laboratory space and could be used as a routine particle size fractionation of soil OM. Finally, this paper lists various methodological aspects of considerable significance but rarely reported in published studies.     

Cation exchange capacities of organo-mineral particle-size fractions in soils from long-term experiments

Soils with and without organic manuring from 10 long-term manurial experiments in East Germany were fractionated into organo-mineral particle-size separates by ultrasonic disaggregation and sedimentation/decantation. The cation exchange capacities (CECs) buffered at pH 8.1 were determined for the size fractions fine+medium clay, coarse clay, fine, medium and coarse silt, sand, and for the total soil samples. In the samples from nine field experiments the CECs decreased with increased equivalent diameters (fine+medium clay: 489–8 13 mmol_c kg^?1, coarse clay: 367–749 mmol_c kg^?1, fine silt: 202–587 mmol_c kg^?1. medium silt: 63–345 mmol_c kg^?1, coarse silt: 12–128 mmol_c kg^?1 and sand: 10–156 mmol_c kg^?1. The CECs varied with genetic soil type, mineralogical composition of the <6.3-μm particles, and the C and N contents of the size fractions. In a pot experiment examining the role of various organic materials in the early stages of soil formation, the clay-size fractions had the largest CECs (85–392 mmol_c kg^?1), followed by the medium-silt (1 9-222 mmol_c kg^?1) and fine-silt fractions (23–192 mmol_c kg^?1). The effect of organic amendments on CEC was in general: compost>fresh farmyard manure = straw + mineral fertilizer = mineral fertilizer.     

Relationships between particle size distribution and VNIR reflectance spectra are weaker for soils formed from bedrock compared to transported parent materials

The cost of determining particle size distribution (psd) of the soil can be significantly reduced by using statistical relationships between visible and near infra red diffuse reflectance spectra (VNIR-DRS) and the proportions of the three size fractions (sand, silt and clay). The spectra contain information on the quantities of soil minerals which occur in these fractions. Statistical models for estimating psd based on a set of soil samples from common parent materials (PM)—with similar mineralogy—may provide more accurate predictions than more comprehensive, global models. The aim of this paper is to compare the performance of statistical models for the prediction of psd from VNIR-DRS for soils with differing types of parent material; specifically soils derived directly from bedrock (coal-bearing and mudstone-bearing strata) or from transported parent materials (glacial till, glacio-lacustrine deposits and alluvium) across eastern England. We assessed the accuracy of psd predictions using partial least squares regression (PLSR) models between two additive log ratios of the three size fractions and VNIR-DRS. We also formed a global PLSR model from all five soil groups. We used mean residual prediction deviation (RPD) from repeated (n = 100) cross-validation to compare the performance of the models because it accounts for the magnitude of variation in the sample data. The most accurate models for the clay (RPD range 1.82-2.33) and sand fractions (RPD range 1.71-1.94) were for soils developed over the transported PM; the models for soils developed over bedrock were substantially poorer (clay RPD range 1.33-1.68; sand RPD range 1.34-1.39). The RPD values for the silt fraction models were smaller, but the same distinction between transported (better; RPD range 1.4-1.88) and bedrock-derived soils (poorer; RPD range 1.15-1.25) was observed. The global model had intermediate RPD values for the three size fractions (clay = 1.75, silt = 1.76 and sand = 1.74). Of the five groups, the soils developed from glacio-lacustrine deposits had the largest mean sand size fraction (58%), but also the most accurate models for estimation of clay and sand size fractions. Due to sedimentary transport and deposition, the mineralogy of the soils developed from Quaternary substrates may be more homogeneous than the bedrock-derived soils, which may in part account for the more accurate models developed for the former. To date we do not have sufficient evidence to demonstrate this unequivocally.     

Linear Regression Models to Estimate Exchangeable Sodium Percentage and Bulk Density of Salt Affected Soils in Sahl El-Hossinia,El-Sharkia Governorate,Egypt

ABSTRACT

The objective of this study was to develop a Linear Regression Model for the prediction of soil bulk density based on organic matter content (OM) and textural fractions (% sand, silt and clay) as well as the soil exchangeable sodium percentage (ESP) based on soil sodium adsorption ratio (SAR) in some salt affected soils of Sahl El-Hossinia, El-Sharkia Governorate, Egypt. For this purpose, 160 samples were randomly taken from top of the surface soil (0–30 cm) from different locations and samples were subjected to various analyzes. XLSTAT Version 2016.02.27444 software was used to build and test conceptual and empirical models. The statistical results of the study indicated that to predict soil bulk density (BD) based on organic matter content and textural fractions the Multiple linear regression model BD = 1.817–0.730 × OM – 0.002 × Clay – 0.001 × Silt with R² = 0.794. On the other hand, to predict soil ESP based on SAR the linear regression model ESP = 5.577 + 0.851 × SAR with R² = 0.773. A Linear Regression Model for prediction of BD and ESP of Sahl El-Hossinia, El-Sharkia Governorate, Egypt, can be used with high prediction.     

The distribution of native and labelled carbon between soil particle size fractions isolated from long-term incubation experiments

Four soils with 6, 12, 23 and 46% clay were fractionated according to particle size after incubation for 5–6 years with ¹⁴C labelled straw, hemicellulose or glucose: 6–23% of the ¹⁴C was still present and the amount increased with increasing content of fine particles. clay fractions contained 66–84% of the ¹⁴C and the silt fractions accounted for 4–19%. <2% was found in the sand fractions and 4–9% was water soluble. The distribution of the native C was: clay, 46–68%; silt, 20–31%; sand, 2–7%. The clay fractions had higher relative proportions of ¹⁴C than of native C, the reverse being true for the silt fractions. This distribution pattern was not directly related to soil clay content or to kind of organic amendment. The C enrichment factor of clay and silt fractions (per cent C in fraction/per cent C in whole soil) increased with decreasing fraction size for both native and ¹⁴C. However, clay enrichment factors were higher for ¹⁴C than for native C, whereas silt enrichment factors were lower. A soil (9% clay) that had been incubated in the field for 18 years with ¹⁴C labelled straw was also analysed. Labelled C content at sampling was 9% of the initial value. In contrast to the other soils the distribution of labelled and native C was similar in the clay and silt fractions, which contained 55% and 33% of the whole soil C, respectively. The results indicate that clay-bound organic matter may be important in mediumterm organic matter turnover, whereas silt-bound organic matter may participate in longer-term organic matter cycling.     

COUNTER DIFFUSION OF Rb86 AND Sr89 IN COMPACTED SOIL

Counter-diffusion coefficients of Rb⁸⁶ and Sr⁸⁹ counter diffusing against H⁺ ions were measured in Dundee silt loam and Sharkey clay soils at differing soil bulk-densities. The cation exchange complex of each soil was saturated with either Rb⁺, Sr⁺⁺, or H⁺ and washed free of salts before making diffusion measurements. The water content of the soil on an oven-dry weight basis was maintained at a constant value for all bulk-densities; 14.2 and 28.0 per cent for the Dundee and Sharkey soils respectively. These moisture contents correspond to a tension of 2/3 bar for sieved soil. The diffusion coefficients were dependent upon concentration. Average counter-diffusion coefficients were calculated and related to soil bulk-density. Soil compaction of Dundee silt loam had little or no effect upon the counter diffusion of Rb⁸⁶. The average counter-diffusion coefficients of Sr⁸⁹ in Dundee silt loam and Sharkey clay were significantly and linearly related to bulk-density; as bulk-density increased the average counter-diffusion coefficients increased. The average counter-diffusion coefficients were approximately 0.5–0.75 of the corresponding self-diffusion coefficients measured previously in these soils. The applicability of counter- and self-diffusion data to practical field problems are discussed.     

Effects of hydroxy-aluminum on flocculation and permeability of silt and clay fractions separated from paddy soils

Flocculation tests and permeability measurements were carried out for silt and clay fractions separated from surface and subsurface horizons of four paddy soils. There was not much difference in the flocculating power between A1(OH)_2.2C1_0.8 and CaSO₄. Their flocculation value, 0.3 to 3 mM, was attained by adding the reagents at the rate of 0.24 to 2.4 mmol/100 g of the silt and clay. The flocculation with A1(OH)_2.2C1_0.8 or CaSO₄ did not affect the sediment volume of the silt and clay. This sediment volume was smaller for the surface than for the subsurface horizons of each soil, suggesting that soil organic matter and repetition of wetting and drying contribute to the stable aggregation of the silt and clay in the surface horizon. The permeability was higher for the silt and clay fractions separated from the surface horizon than that from the subsurface horizon, and the addition of 2.5 to 4.2 mmol of A1(OH)_2.2C1_0.8 or CaSO₄/100g of the silt and clay increased its permeability by 1.5 to 4 times. The effect of A1(OH)_2.2C1_0.8 was more lasting than that of CaSO₄ and was recognized even after 200 ml of water passed through 1 g of the silt and clay. The effect of the flocculating reagent on the permeability was more or less enhanced by air-drying the treated silt and clay.