THE DISTRIBUTION OF LABELLED SUGARS IN SOIL PARTICLE SIZE FRACTIONS AS A MEANS OF DISTINGUISHING PLANT AND MICROBIAL CARBOHYDRATE RESIDUES

Soils of the Countesswells and Insch series incubated with ¹⁴C labelled glucose or plant materials have been separated into clay (< 2 μm), silt, (2–20 μm), fine sand (20–250 μm) and coarse sand (>250μm) fractions and the distribution of individual labelled and unlabelled sugars was determined in each fraction. Both soils contained about 10–15 per cent clay, 18–23 per cent silt and about 60 per cent fine and coarse sand. For all soil samples the concentrations of sugars were usually greatest in the clay, slightly less in the silt, with values in the sand fractions being five or ten times lower, except when fresh plant material was present. In ¹⁴C glucose amended Insch soil, 55 per cent of the radioactivity in sugars (predominantly hexoses) occurred in the clay, 36 per cent in the silt, 3 per cent in the fine sand and 6 per cent in the coarse sand after 28 days incubation. For the Countesswells soil the values were 55, 42, 2 and 1 per cent respectively. In ¹⁴C ryegrass amended soil before incubation. 77 per cent of the radioactivity in sugars (predominantly glucose, arabinose and xylose) was in the coarse sand. After one year's incubation this had fallen to 59 per cent. In soil amended with ¹⁴C cereal rye straw the distribution of radioactivity in sugars after four years incubation was: clay, 21 per cent; silt, 43 per cent; fine sand, 21 per cent; coarse sand, 4 per cent. These distributions were compared with that of the naturally occurring sugars: clay, 31–42 per cent; silt, 40–43 per cent; fine sand, 3–11 per cent; coarse sand, 12–20 per cent.     

THE INFLUENCE OF TEXTURE ON THE MOISTURE CHARACTERISTICS OF SOIL

A quantitative assessment was made of the effect of the proportion of sand, silt, clay, and organic matter in twenty-six soils on the moisture contents at the upper and lower limits of available-water of the soils. Regression equations were obtained which enabled the moisture contents to be estimated on a weight or volume basis from mechanical analysis data using either International or American size grades. The accuracy of estimating the upper limit of available-water from the various equations ranged from ±9 to 22 per cent: for the lower limit from ±8 to 16 per cent of the measured values. Mean values of the moisture contents at the upper and lower limits of available-water for each textural class were calculated from the average particle-size composition for each class and from the regressions obtained.     

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.     

MINERALOGY AND RADIOISOTOPE RETENTION PROPERTIES OF A CHRONOSEQUENCE OF SOILS DEVELOPED IN BASALTS OF VICTORIA, AUSTRALIA

The mineralogical composition and retention properties for radioisotopes (²⁰Sr and ¹³⁷Cs) of soils developed in five basalt flows of age varying from 6000 years to about four million years occurring in western Victoria were investigated. The trend of mineral weathering has been almost exclusively to amorphous material, kaolinite-plus-halloysite, and chlorite, the more soluble products of weathering having been removed. The most significant changes in clay mineralogical composition with time are the progressive decrease in the Si0₂/Al₂O₃ molar ratio of the amorphous material in the clay fraction of the surface horizons, from an initial value of approximately 4 to values of approximately 2, and the progressive increase in the amount of kaolinite-plus-halloysite, both in the topsoil and at depth, with age of the basalt flow. The amount of kaolinite plus halloysite increases from approximately 20 per cent of the clay of soil developed in the basalt flow 6000 years old to approximately 50 per cent of that of soil in basalt about four million years old. Evidence for the presence of halloysite was obtained by electron microscopy studies. The amorphous material and chlorite contents, each of which constitutes between 20 and 50 per cent of the clay fractions, decrease concurrently with the increase in kaolinite-plushalloysite content. Fixation of Sr by whole soil samples was controlled by the organic matter and free iron oxide contents rather than by the mineralogy of the samples. A high proportion of the added Cs was sorbed by whole soil samples. Much of the sorbed Cs was not readily replaced by CaCl, washings but was replaced in part by subsequent washing with NaCl of pH 5.3 and almost entirely by subsequent NH₄Cl washings. Much of the Sr and Cs deposited on these soils by rainfall and dry fall-out would be sorbed; the ease of replacement suggests that these elements would be available for further movement through the food chain.     

THE INFLUENCE OF TEXTURE ON THE MOISTURE CHARACTERISTICS OF SOILS

A quantitative assessment was made of the effect of the proportion of sand, silt, clay, and organic matter in twenty-six soils on the available-water capacities (AWC) of the soils. The AWC of a soil was negatively correlated with percentage coarse sand and positively correlated with the percentages of International fine sand (or American silt) and organic C. Using a regression equation, the AWC's of the soils were estimated from mechanical analysis data with a mean accuracy of ± 16 per cent of the mean AWC.     

PROCESSES OF HUMUS FORMATION AND TRANSFORMATION IN SOILS OF THE CANADIAN GREAT PLAINS

A study of the A horizons of cultivated soils from Saskatchewan, Canada showed that the organic carbon contents were in the sequence semi-arid Dark Brown soils (1.7 per cent), < Black soils (2.55–2.8 per cent), < sub-humid Dark Gray soils (4.5 per cent). The relative proportions of humic acids and the ratios of humic acid: fulvic acid increased in a similar sequence. There were accompanying increases in extinction values at 280 nm, and in levels of nonhydrolyzable nitrogen suggesting more extensive polycondensation of humic materials. These observations are discussed in terms of a working hypothesis for humus formation and transformations, that gives particular emphasis to the soil environment and to interactions between organic and inorganic components.     

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.     

CLAY MINERAL DISTRIBUTION AND ORIGIN IN THE SOIL TYPES OF ISRAEL

The mineralogical composition of clays (< 2μm) in representative profiles of all soil types of Israel was investigated. The soils were classified according to their clay mineral assemblages into three groups. I. Montmorillonitic soils. Montmorillonite is the dominant mineral and exceeds 65 per cent of the total minerals found; each of the other minerals comprises less than 15 per cent. 2. Montmorillonitic-kaolinitic soils. The soil clay fractions contain 50-60 per cent montmorillonite and 15-25 per cent kaolinite, generally adding up to more than 75 per cent of the clay fraction. 3. Montmorillonitic-calcitic soils. The clays contain more than 10 per cent calcite. Montmorillonite is the dominant clay mineral (except for one soil type, mountain rendzina, where calcite is dominant). The first and second assemblages are typical of the soils of the Mediterranean zone, whereas the soils of the desert zone are characterized by the third assemblage. The origin of montmorillonite, kaolinite, and illite, the three main clay minerals, was found to be detritic, as was the origin of palygorskite which was mainly found in the calcite rich soils of the desert zone. The cation exchange capacity of montmorillonite seems to be higher under higher precipitation. Montmorillonite content and cation exchange capacity of the clays were found to be highly correlated. The carbonate content of the clay fraction and the amount of carbonate in the soil were also highly correlated.     

Land-use effects on the composition of organic matter in particle-size separates of soil: I. Lignin and carbohydrate signature

Soil from Eutrochrept A horizons under long-term spruce forest (Sf), mixed deciduous forest (Df), permanent grassland (Gp) and arable rotation (Ar) was fractionated according to particle size and analysed for contents of C, N, lignin-derived phenols and carbohydrates. Whole soil from Sf, Df, Gp and Ar contained 84, 59, 73 and 25 g C kg^?1 soil, respectively. For all sites, the C content declined and C/N ratio increased in the order: clay (<2 μm), silt (2–20 μm), sand (20–2000 μm). Clay and silt were significantly lower in C in Ar than in Sf, Df and Gp, C associated with sand being substantially lower under arable rotation. The yield of lignin-derived phenols decreased and carboxyl functionality and methoxyl demethylation of lignin derivatives increased with decreasing particle size, indicating a progressive lignin alteration. Whole soil from Sf and Gp was substantially higher in vanillyl (V), syringyl (S) and cinnamyl (C) units (VSC) than soil from Df and Ar. Compared to whole soil, clay was depleted and sand enriched in VSC. Only sand appeared to be affected significantly by land use. Sand from Ar and Df was more enriched in VSC than sand from Gp and Sf. Whole soil carbohydrates decreased in the order: Gp>Ar>Df>Sf. Sand- and clay-sized separates were enriched in carbohydrates compared to silt. Carbohydrates in sand were mainly of plant origin whereas microbially-derived sugars accounted for a larger proportion in the clay. Compared to Sf, Df and Gp, clay from Ar was enriched and sand depleted in microbial sugars. Lignin and carbohydrate distribution patterns indicate that organic matter was in a more advanced stage of decomposition in the sand separates from forest than from agricultural A horizons. The forest soils also show a higher degree of oxidative changes in lignin associated with clay. In contrast, differences between silt from the four A horizons were small.     

THE CONTENTS AND SORPTION OF CADMIUM IN SOME AGRICULTURAL SOILS OF ENGLAND AND WALES

Cadmium sorption was measured in 10 agricultural soils with pH ranging from 4.5 to 7.9, and total Cd content from 0.27 to 1.04 μg g^?1 dry soil. With initial Cd concentrations of 0.5 to 100.0 μM, sorption from 0.002 M CaCl₂ was described by the Freundlich adsorption equation but the gradients of the isotherms increased when the initial concentrations were below 0.5 μm. This indicates that there are specific sites of differing sorption energy; differences between soils in the gradients of the isotherms at low initial concentration could largely be accounted for by their contents of ‘free’ Fe₂O₃. When initial concentrations were below 0.5 μm there was a linear relationship between the quantity of Cd sorbed and the final concentration in solution. This relationship held with all soils except that of lowest pH from which there was a net loss of Cd to the solutions. Desorption was measured from three soils with contrasting pH. With the soil of lowest pH, over 80 per cent of sorbed Cd was desorbed to 0.002 m CaCl₂ and up to 30 per cent to 100 or 500 μm solutions of heavy metal chlorides. In contrast, only very small proportions (<1.25 per cent) were desorbed from the other soils with pH 6.7 and 7.8. The results indicate that Cd is strongly sorbed by soils of pH of above 6.0 when added in amounts comparable to additions in sewage sludges or phosphatic fertilizers, and illustrate the importance of liming as a means of reducing the mobility of this metal in soils.     

The influence of clay on the rate of decay of amino acid metabolites synthesized in soils during decomposition of cellulose

¹⁴C-labelled cellulose was added to seven different soils containing silt + clay (particles < 0.02 mm) in amounts which varied from 8 to 75 per cent. The cellulose was allowed to decompose, and the amounts of labelled C transformed into metabolites hydrolyzable into amino acids were determined. The amounts of labelled amino acid C in the soils were proportional to their content of silt + clay. After 30 days of incubation labelled amino acid C remaining in the soil with the lowest content of silt + clay constituted 6 per cent of the carbon added in cellulose, as compared with 18 per cent in the soil with the highest content of silt + clay. These values had decreased to 5 and 13 per cent respectively after 2 years of incubation. The order between the soils in the content of labelled amino acid C established during the first month of incubation, was thus roughly maintained throughout the period of incubation. The biological half-life of the labelled C in amino acids varied in the seven soils during the last year of incubation from 3 to 8 years. The variation was, however, not related to the amount of silt + clay.n the soils had been incubated with the labelled material for 2 years, samples of the soils were exposed to “stress” treatments: air drying-rewetting; increased biological activity caused by addition of glucose, and exposure to chloroform vapour. The treatments resulted in an evolution of labelled C in CO, which was 5–10 times larger than the evolution from untreated samples. The increase in the CO₂ evolution caused by the treatments in the different soils was, however, not related to the amount of silt + clay, and a high content of this material did not protect organic material against the effect of the treatments.is concluded that the silt + clay fraction ensures stabilization of amino acid metabolites produced during the period of intense biological activity that follows the addition of decomposable, energy rich material to the soil. The amount of amino acid metabolites stabilized increased with increasing concentration of silt + clay, but the rate of decay of the amino acid material during later stages was largely independent of the concentration of silt + clay.     

THE ORGANIC MATTER CONTENT OF THE SAVANNA SOILS OF WEST AFRICA

Published and unpublished data on the amounts of organic matter and nitrogen in the surface soils of the West African savanna are reviewed. In general, amounts are small; the mean carbon content of soils from 605 well-drained sites was 0.68 per cent. Two important factors governing amounts of organic matter in well-drained soils appear to be the clay content and a moisture factor related to the length of the wet season and represented here by mean annual rainfall. Multiple linear regression on soil clay content and rainfall accounted for 46.5 per cent and 57.2 per cent, respectively, of the observed variability of soil carbon and nitrogen contents. These findings suggest that the low levels of organic matter in savanna soils arise from their predominantly sandy nature and from the relatively low rainfall. In poorly drained soils organic matter levels are higher but are less significantly related to clay content and rainfall. The influence of human interference and of parent material and altitude on organic matter is demonstrated in the context of geographically limited areas within the savanna for which more detailed information was available.     

皖南山地主要土壤的特征和分类问题

本文研究了皖南山地主要土壤的特征和分类。结果表明,本区土壤风化和淋溶作用强,富铝化特征明显,且随海拔高度的增加,土壤特征有差异。海拔600-700m以下的土壤,B层颜色以红棕色和亮红棕色(5YR5/6-5/8)为主,粉砂/粘粒值小于1.00,风化淋溶系数小于0.35,盐基饱和度小于35%,粘粒SiO₂/Al₂O₃多小于2.4。粘粒矿物以高岭石为主。氧化铁的活化度和络合度低,表层HA/FA小于0.35。该类土壤定为黄红壤(红壤土类中的一个亚类)。海拔600-700m以上的土壤,B层颜色以黄色(2.5Y8/6)和亮黄棕色(10YR6/6-6/8)为主,粉砂/粘粒值大于1.00,风化淋溶系数大于0.35,盐基饱和度小于35%,粘粒SiO₂/Al₂O₃一般大于2.3。粘粒矿物以蛭石和高岭石为主,并有较多的三水铝石出现。氧化铁的活化度和络合度高,表层HA/FA值0.35-0.75。该类土壤定为黄壤。从粘粒矿物组成和SiO₂/Al₂O₃,判断,皖南山地上部不存在山地黄棕壤和山地棕壤。土壤垂直带谱主要由黄红壤和黄壤构成。     

Occurrence and genesis of secondary magnesium-bearing calcites in soils

The presence of magnesium-bearing calcites is indicated in soil carbonate accumulation layers and concretions. A differential solubility method permitted estimation of the mol percent magnesium-carbonate content of calcites in the presence of dolomite. The relationship between diffraction spacings and mol percent MgCO₃, of selected samples is in good agreement with that depicted by other workers for biogenic magnesium-bearing calcites.Magnesium-containing calcites are concentrated in clay (< 2 μ) and fine silt (2–10 μ) sizes of Cca horizons. Their presence in the clay fraction of Ck horizons is an indication that carbonate mineralogy may change at profile depths often considered to be unaffected by pedogenic processes.The dissolution of existing carbonates within solum horizons, the translocation of ions in solution and the reprecipitation of calcite in Cca and underlying horizons are the main processes applicable to a variety of different natural situations. The Mg level of the secondary calcites is likely regulated by the partitioning effect during their precipitation. Periodic moisture movement to greater depths and lateral movement of soil solutions serve as a regulating factor in maintaining soluble Mg at levels favorable to the precipitation of low-magnesium calcites in upland chernozemic soils of central Saskatchewan; higher magnesium contents occur in calcites occurring in subsoils underlying solonetzic and depressional chernozemic soils of the same area. Formation of magnesium-bearing calcites within concretions in soils of the Rusizi basin in Africa were likely influenced by Mg-rich ground waters; associated dolomite may also have been of a secondary nature.     

REACTIONS OF SOLUBLE PHOSPHATE WITH ACID SOILS: THE INTERPRETATION OF ADSORPTION-DESORPTION ISOTHERMS

Adsorption-desorption and isotopic-exchange isotherms for acids soils of known clay mineralogy indicated that when all the surfa? P accessible to the solution was considered, the bonding energy for phosphate decreased exponentially with site coverage. The soils differed markedly in the quantities of surface P held at sites of very high bonding energy, defined as those in equilibrium with a solution concentration < 1 μM; the values ranging from 9 μmol g^?1 in a soil with 40 per cent gibbsite in the clay fraction, to 1 μmol g^?1 in a soil with only 1 per cent gibbsite and no interlayered material. The reversibility of current P adsorption on soil surfaces depended on the immediate history of the soil sample. Complete reversibility occurred when soil, previously enriched with soluble P and stored for 4 to 5 months at constant temperature, was suspended in solutions of constant pH and ionic strength. It is suggested that irreversibility occurs due to incomplete attainment of equilibrium during the adsorption phase, a condition predisposed by high initial P concentrations (>1mM), and the use of soils that are naturally in dis-equilibrium because of recent fertilizer additions or severe depletion of P by plant uptake.     

EXCHANGEABLE SODIUM AND YIELDS OF COTTON ON CERTAIN CLAY SOILS OF SUDAN

Within Sudan there are extensive areas of Vertisols in the Nile River valley south of Khartoum. These soils have clay contents ranging from 40 to 60 per cent, very slow permeability, exchangeable sodium percentages up to 35 or more in the upper 60 cm, and pH values between 8.0 and 9.6. Under present management, satisfactory yields of long staple cotton are obtained under irrigation on soils having exchangeable sodium percentage (ESP) of up to 35 in the upper 60 cm. It is proposed that soil characteristics such as type of clay, cracking and exchangeable sodium in the hot, dry climate of Sudan influence soil structure and water availability and thus the yields of cotton.     

CHEMICAL AND MINERALOGICAL PROPERTIES OF BROWN PODZOLIC SOILS IN COMPARISON WITH SOILS OF OTHER GROUPS

Chemical and mineralogical properties of brown podzolic soils, brown earths, a podzol, and an Andept have been studied with particular reference to the kinds and distribution of amorphous materials. In addition to pyrophosphate extractable (Fe + Al)/per cent clay, brown podzolic soils can be distinguished from brown earths by Fe-oxalate/Fe-dithionite and Fe-pyrophosphate/Fe-dithionite ratios, fluoride reactivity, and the presence of intergrade 2:1-2:2 and smectite-like clay minerals in surface horizons. Significant amounts of amorphous alumino-silicates resembling allophane were found in the Bs horizons of the brown podzolic soils, particularly those on igneous rocks. These amounts are sufficiently large to suggest the recognition of an Andic sub-group of brown podzolic soils in England and Wales.     

Assessing and mapping topsoil organic carbon stock at regional scale: A scorpan kriging approach conditional on soil map delineations and land use

In order to assess the potential of soils as C reservoir at regional scale, accurate estimates of soil organic carbon (SOC) are required, and different approaches can be used. This study presents a method to assess and map topsoil organic carbon stock (Mg ha⁻¹) at regional scale for the whole Emilia Romagna plain in Northern Italy (about 12 000 km²). A Scorpan Kriging approach is proposed, which combines the trend component of soil properties as derived from the 1:50 000 soil map with geostatistical modeling of the stochastic, locally varying but spatially correlated component. The trend component is described in terms of varying local means, calculated taking into account soil type and dominant land use. The resulting values of SOC, sand, silt, and clay contents are retained for calculating topsoil SOC stocks, using a set of locally calibrated pedotransfer functions (PTFs) to estimate bulk density. The maps of each soil attribute are validated over a subset of 2000 independent and randomly selected observations. As compared to the standard approach based on the mean values for delineation, results show lower standard errors for all the variables used for SOC stock assessment, with a relative improvement (RI) ranging from 4 per cent for SOC per cent to 24 per cent for silt. The total C stock (0–30 cm) in the study area is assessed as 73·24 ± 6·67 M t, with an average stock of 62·30 ± 5·55 Mg ha⁻¹. The SOC stock estimates are used to infer possible SOC stock changes in terms of carbon sequestration potential and potential carbon loss (PCL). Copyright © 2010 John Wiley & Sons, Ltd.     

THE EFFECT OF SOIL FACTORS ON THE EXTRACTION OF SOIL ORGANIC MATTER BY ANHYDROUS FORMIC ACID

Twenty-five soils, having a wide range of organic matter contents, were extracted with anhydrous formic acid containing 10 per cent acetylacetone, and the extracted material precipitated in two fractions with diisopropyl ether. Precipitates comprised from 5.1 to 51.1 per cent of the original soil organic matter, the proportion extracted tending to be greatest from acid soils of fairly high organic matter content and least from neutral or slightly alkaline soils of low organic matter content. Soil clay content appeared to have no effect on the efficiency of organic matter extraction, but was the most important soil factor governing the proportion of the total soil-N extracted. Amounts of N extracted ranged from 10.2 to 57.8 per cent of the original soil N content, extraction efficiency being greatest with soils of low clay content and low pH. There was evidence to suggest that soil clay afforded some protection to N compounds against extraction. The results indicate that formic acid/acetylacetone is most effective with soils in which much of the organic matter is only partly humified.     

Klimaeinfluß auf Lignin und Polysaccharide in Partikelgrößen-Fraktionen zonaler Steppenböden Rußlands

Climatic effect on lignin and polysaccharides in particle-size fractions of zonal steppe soils, Russia Zonal soils derived from similar parent materials are suitable for investigating the question, whether and how climate affects soil organic matter properties. For this reason we sampled 10 native surface (0—10 cm) and subsurface (ca. 50—60 cm) soil horizons in the native steppe and forest steppe of Russia. Polysaccharides and the vanillyl, syringyl and cinnamyl structural units of lignin (VSC) were determined in the fine earth (< 2 mm) as well as in clay (< 2 μm) and silt (2—20 μm) fractions. As the ratio of mean annual precipitation to potential evaporation (N/V) decreased, the concentrations of polysaccharides tended to decrease in the subsoil horizons. This was indicated most clearly for the silt fractions (r = 0.98**). In contrast, the VSC contents (in g kg^—1 organic C) of the subsoils increased as N/V decreased (r = —0.92*), resulting in increasing VSC/polysaccharide ratios of the subsoil horizons with decreasing N/V ratio (r = —0.94*). It is suggested that production of polysaccharides or their transport into the mineral subsoil or both is favored at sites with wide rather than narrow N/V ratio, whereas lignin might be selectively enriched during intense soil organic matter decay at the Southern sites.