Influence of the nature of clay minerals on the fixation of radiocaesium traces in an acid brown earth–podzol weathering sequence

The magnitude of radiocaesium fixation by micaceous clay minerals is affected by their transformation, which depends on weathering in soil. The net retention of radiocaesium traces was quantified by sorption–desorption experiments in the various horizons of four sandy soils forming an acid brown earth–podzol weathering sequence derived from sandy sediments and characterized by marked changes in mineral composition. The features of the 2:1 minerals of the four soils, resulting from an aluminization process in depth and a desaluminization process towards the surface, had a strong influence on Cs⁺ fixation. Beneath the desaluminization front, which deepens from the acid brown earth to the podzol, hydroxy interlayered vermiculite was dominant and the ¹³⁷Cs⁺ fixation was the weakest. At the desaluminization front depth, vermiculite was responsible for the strongest ¹³⁷Cs⁺ fixation. In the upper layers, smectite appeared in the podzolized soils and the ¹³⁷Cs⁺ fixation decreased. The magnitude in Cs⁺ fixation therefore appeared as a tracer of the transformation process affecting the 2:1 clay minerals in the acid brown earth–podzol weathering sequence. This magnitude was positively correlated with the vermiculite content of the studied soil materials estimated by the rubidium saturation method.     

Interaction forces between soil particles: shear moduli of the < 2 μm size fraction

The shear moduli of the < 2 μm size fraction of three soils have been measured for samples of 10–35% w/w solid. Samples were thixotropic, the shear modulus increasing with time. This increase can be described by simple models and visualized in terms of the formation of links between particles. For a given soil the shear modulus increases with ionic form in the order Ca²⁺∼Mg²⁺ + + < Li⁺ and varies in a complex manner with electrolyte concentration.     

Long-term application of animal slurries to grassland alters soil cation balance

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.     

Ca2+ Effects on K+ Fluxes in Arabidopsis Seedlings Exposed to Al3+

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.     

Formation of 2,4–D complexes on montmorillonites – an ab initio molecular dynamics study

Sorption of the anionic form of the pesticide 2,4–D (2,4–dichlorophenoxyacetic acid) on the surface of the clay mineral montmorillonite was investigated using a short-time ab initio molecular dynamics (MD) simulation at room temperature. Three different situations were modelled: sorption on a dry surface, on a hydrated surface and an intercalation between montmorillonite layers. In all three cases, the calcium cation compensates the excess negative charge of the montmorillonite layer and the negative charge of the 2,4–D anion. It was found that in all models with direct contact of the Ca²⁺ cation with the montmorillonite layer, the most stable position of Ca²⁺ is above the ditrigonal hole of the mineral layer. While in the case of a dry surface very stable bidentate binding is created between the 2,4–D anion and the Ca²⁺ cation, the formation of the monodentate complexes is preferred in all models that include water molecules. Hydrogen bonds formed between water molecules and the 2,4–D anion make a considerable contribution to the formation of the monodentate complexes. Tetrahedral substitutions in the montmorillonite layer have a significant effect on the formation of the complexes of any type. However, the MD simulations did not support the role of Ca²⁺ as a cation bridge in the adsorption mechanism. Calculations showed that hydrated 2,4–D···Ca²⁺ complexes are thermodynamically more stable than complexes in which the Ca²⁺ cation acts as a bridge to the surface. On the other hand, it is possible that phyllosilicates with a greater concentration of isomorphic substitutions (e.g. mica) will be able to form stable surface complexes with a cation bridge mechanism.     

Analysis of Potassium Uptake by Rice Roots Treated with Aluminum Using a Positron Emitting Nuclide, 38K

We investigate the effect of Al on K⁺ uptake by rice roots. Potassium-38 (³⁸K), a positron emitting nuclide (the half-life: 7.61 min), was used to trace K⁺ behavior. When a rice root was treated with 10μM Al for 24 h, the uptake of ³⁸K in the root was increased in the range of 1 to 2 cm from the root tip compared with that of the control sample. Because the root continued to grow without showing any damage of plasma membrane during the Al treatment, it was suggested that the ³⁸K uptake was not occurred through diffusion into the cells. The uptake of ³⁸K in both treatments, with/without Al, was decreased by VO₄^3- (inhibitor of H⁺-ATPase on plasma membrane) and DNP (H⁺ ionophore) treatment, which suggested that the K⁺ uptake was performed through an active transport, such as H⁺:K⁺ transport or H⁺ gradient promoted by an Al treatment.     

Correlations between extractable Na, K, Mg, Ca, P & N from fresh and dried samples of two Aquults

Significant increases in extractable ions resulted from air-drying and grinding samples of two infertile Aquults. Effects of the sample preparation differed markedly between ions and between the two soils. Regression equations were calculated to predict extractable ions in dried, ground samples from extractable ions in fresh, unground samples and the relationships were compared between the two soil series. Regressions were significantly different between soils for extractable PO³₄, Mg⁺⁺, and K⁺, but not for Ca⁺⁺ and Na⁺. Extractable NH ⁺₄ and NO-₃ in fresh, unground samples were not correlated with those in air-dry, ground samples of either soil. Differences in response to preparation between soil types appeared to be related to the oxidative status of these soils in the field, wherein constituents of more poorly-drained soils may be less stable to the oxidizing conditions of air-drying and grinding. Such complexities suggest that effects of sample preparation should be considered when interpreting soil nutrient data for studies of forest nutrient cycling and forest soil fertility.     

A world dataset of derived soil properties by FAO–UNESCO soil unit for global modelling

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.     

Effects of the nitrification inhibitor dicyandiamide on potassium, magnesium and calcium leaching in grazed grassland

Abstract. Leaching of calcium (Ca), potassium (K) and magnesium (Mg) from urine patches in grazed grassland represents a significant loss of valuable nutrients. We studied the effect on cation loss of treating the soil with a nitrification inhibitor, dicyandiamide (DCD), which was used to reduce nitrate loss by leaching. The soil was a free-draining Lismore stony silt loam (Udic Haplustept loamy skeletal) and the pasture was a mixture of perennial ryegrass ( Lolium perenne ) and white clover ( Trifolium repens ). The treatment of the soil with DCD reduced Ca²⁺ leaching by the equivalent of 50%, from 213 to 107 kg Ca ha⁻¹ yr⁻¹ on a field scale. Potassium leaching was reduced by 65%, from 48 to 17 kg K ha⁻¹ yr⁻¹. Magnesium leaching was reduced by 52%, from 17 to 8 kg Mg ha⁻¹ yr⁻¹. We postulate that the reduced leaching loss of these cations was due to the decreased leaching loss of nitrate under the urine patches, and follows from their reduced requirement as counter ions in the drainage water. The treatment of grazed grassland with DCD thus not only decreases nitrate leaching and nitrous oxide emissions as reported previously, but also decreases the leaching loss of cation nutrients such as Ca²⁺, K⁺ and Mg²⁺.     

Metal-humus complexes in A horizons of Thai and Korean red and yellow soils

Carbon, Al and Fe (C_pyr, Al_pyr and Fe_pyr) were extracted with 0.1 m Na₄P₂O₇ from 26 A horizon samples of tropical Thai and temperate Korean soils (Ultisols, Alfisols, Oxisols and Inceptisols). The soils, except for one Thai Inceptisol, had similar total C (0.35–3.29%) and C_pyr/total C ratios (0.20–0.41). There were approximately linear relationships between total C or C_pyr and clay content; two groups of soils gave different linear relationships. A curvilinear relationship between C_pyr and (Al + Fe)_pyr (milli-atom kg⁻¹) that can be approximated by an equation: C_pyr= 53 (Al_pyr+ Fe_pyr)^1/2– 24 was also found for most Thai and Korean soils. The above relationships indicated that total C and C_pyr would be close to zero at zero clay or zero (Al + Fe)_pyr. It was inferred that clay-humus interaction has a primary importance in the determination of humus content in red and yellow soils in tropical and temperate regions and that the main role of clay is to supply Al and Fe that complex and stabilize humus against microbial degradation.     

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.     

Caesium and strontium diffusion through sodium montmorillonite at elevated temperature

Counter ionic migration rates of dilute Cs⁺ and Sr²⁺ against sodium in a Na-montmorillonite gel are measured using a radially perfused diffusion cell. Enhanced or surface diffusion for caesium is observed both at ambient and elevated temperature. To quantify these surface diffusivities the ion-exchange properties of the diffusing species are required. Thus, exchange isotherms for caesium against sodium on montmorillonite at 22 and 90°C are given for 10⁻¹, 10⁻², and 10⁻³M background NaCl concentrations. Caesium counterion surface diffusivities at 22 and 90°C are 2.2*10⁻⁶ and 8.0 * 10⁻⁶ cm² s⁻¹, respectively. These values are found to be essentially independent of background ionic strength over the range 10⁻³ to 10⁻¹ m NaCl. Experimental evidence of enhanced transport through Na-montmorillonite for the divalent cation Sr²⁺ is also confirmed with a surface diffusivity of 2 * 10⁻⁶ cm² s⁻¹ at 22°C and in 10⁻¹ m NaCl.     

Effects of organic matter and calcium on soil structural stability

The cationic bridging effect of the calcium ion (Ca²⁺) and the flocculating ability of clay and organic matter are crucial in the formation and stability of soil aggregates. They are therefore likely to influence the soil's saturated hydraulic conductivity ( K _s). We tested the individual effects of these factors on aggregate stability and related hydraulic properties, and studied the influence of clay mineralogy also. Samples from the surface (0–10 cm) of three contrasting soils in Trinidad were used. The soils were treated with three levels of Ca²⁺ and three levels of organic matter in a 3 × 3 × 3 factorial design and incubated for 14 days. Both aggregate stability and saturated hydraulic conductivity were influenced by all factor combinations. Interactions between soil type and Ca²⁺ revealed the importance of polyvalent cations in aggregate stability of soils with low activity minerals. The influence of organic matter varied with quantity; the more there was, the more stable the soil became, particularly in the soil containing little clay. Clay dispersion and slaking of expanding minerals occurred even with large additions of Ca²⁺ and organic matter, emphasizing the overall influence of mineralogy in determining the response of soils to stability treatments.     

Effects of ridging on crop performance and symbiotic N2 fixation of fababean (Vicia faba L.)

Abstract. The success of organic cropping systems depends on symbiotic N₂ fixation by leguminous crops, and it is important to explore new management systems to improve the nitrogen input through N₂ fixation. During two growing seasons the possible advantage of growing fababean ( Vicia faba L.) in ridges was studied in comparison to the traditional method on flat soil. Differences in soil physical parameters resulted in a significantly greater microbial activity and a deeper root system at the flowering stage when grown in the ridge than on the flat. Consequently, the amount of fixed N at flowering was significantly greater in ridges than in flat soil. However, during the period from flowering until harvest, when the major part of the N uptake and N₂ fixation took place, the differences between the treatments disappeared. Average values for the growing season of fluorescein diacetate hydrolysis, arylamidase activity and arylsulphatase activity were significantly greater in the ridge than on the flat, and the microbial biomass-C, derived from substrate induced respiration (SIR), was on average 232 and 223 μg C g⁻¹ soil in the ridge and on the flat, respectively. Measured total-N uptake, including root N (0–30 cm depth), ranged from 206 to 247 kg N ha⁻¹, of which 182–201 kg N ha⁻¹ was fixed N. From 154 to 173 kg N ha⁻¹ was removed in grain resulting in a soil-N balance of +28 kg N ha⁻¹ in both years. However, by including estimates of total root N and rhizodeposition-N the soil-N balance ranged from +52 to +62 kg N ha⁻¹.     

Estimation of the density of the protocatechuate-degrading bacterial community in soil by real-time PCR

The β-ketoadipate pathway is the major route for degradation of aromatic compounds by various soil microorganisms. Protocatechuate 3,4-dioxygenase, a key enzyme of this pathway and which is encoded by pcaGH genes, catalyses the ring cleavage of protocatechuate. Microorganisms harbouring pcaGH genes are widely distributed in the environment but little is known about their relative abundance within the total microflora. Hence, this paper reports the development of a real-time PCR assay to quantify the bacterial pcaH sequence that encodes the β sub-unit of the protocatechuate 3,4-dioxygenase. This real-time PCR assay was linear over seven orders of magnitude with a calculated efficiency of 99% and sensitive up to 10² copies of the pcaH sequence per assay. Real-time PCR analyses performed on six soils with different physico-chemical properties, revealed pcaH densities ranging from 10³ to 10⁴ copies of pcaH  ng⁻¹ of soil DNA, which corresponded to approximately 0.2–10.9% of the total bacterial community. The sequencing of real-time PCR amplicons yielded 48 deduced amino acid sequences that exhibited 44–100% identity to known bacterial PcaH sequences, thereby confirming the accuracy of this real-time PCR assay.     

Acid deposition at Rothamsted, Saxmundham and Woburn, 1969–83

Abstract. Rainfall has become less acid at Rothamsted and Saxmundham over the period 1969–83. The pH of rain at these two sites has increased from 4.4–4.6 to about 4.8–4.9; at Woburn it has remained approximately constant at 4.4–4.6. Amounts of NH₄-N and NO₃-N deposited at present are 10–15 and 5–10 kg ha⁻¹ a⁻¹ respectively. They have been increasing at Rothamsted and Woburn. Some 50–60 kg ha⁻¹ a⁻¹ of Cl and 25–35 kg ha⁻¹ a⁻¹ of SO₄-S are presently deposited. Deposition of non-sea Cl and SO₄-S has been increasing markedly at all three sites. Non-sea salts comprise 35% of the total salt deposition near the coast at Saxmundham, 58% inland at Rothamsted and Woburn.     

Effect of supplied phytosiderophore on 59Fe absorption and translocation in Fe-deficient barley grown hydroponically in low phosphorus media

Hydroponically grown barley plants ( Hordeum vulgare L. cv. Minorimugi) under iron-deficient (–Fe) and high phosphorus (P) conditions (500 µmol L⁻¹) showed Fe chlorosis and lower growth compared with plants grown in –Fe and low P conditions (50, 5 and 0.5 µmol L⁻¹). To understand the physiological role of P in regulating the growth of plants in –Fe medium, we carried out an Fe feeding experiment using four P levels (500, 50, 5 and 0.5 µmol L⁻¹) and phytosiderophores (PS), mugineic acid. Our results suggest that plants grown in a high P medium had higher absorption activity of ⁵⁹Fe compared with plants grown in low P media, irrespective of the presence or absence of added PS. Translocation of ⁵⁹Fe from roots to shoots was not affected by the P level. The relative translocation rate of ⁵⁹Fe increased with decreasing levels of P in the medium. In general, the addition of PS enhanced the absorption of ⁵⁹Fe and its translocation. Taken together these results suggest that the lower relative translocation rate of Fe in high P plants may be induced by the physiological inactivation of Fe in the roots, and the higher absorption activity of Fe in high P conditions possibly results from the response of barley plants to Fe deficiency.     

Inhibition of nitrate accumulation in tropical grassland soils: effect of nitrogen fertilization and soil disturbance

In acid soils in the Eastern Plains of Colombia, forage grasses planted on land prepared before the previous dry season produced 40–50% more dry matter than when land was prepared immediately before planting. Virtually no NO₃⁻ accumulated in surface (0–10 cm) soil from three native undisturbed savanna sites. Where land was ploughed before the dry season, NO₃⁻ levels increased gradually after a 2–3 month lag, and dropped at the beginning of the rains. In samples incubated for 4 weeks, more NO₃⁻ accumulated in the wet than the dry season. A similar 2–3-month lag occurred when land was ploughed after the dry season. NH₄⁺ levels were higher in ploughed than savanna soils, and rose in all soils at the beginning of the rains. More NO₃⁻ and NH₄⁺ accumulated on incubation in pots than in soil cores. Forage grasses inhibited NO₃⁻ accumulation in the soil, relative to plant-free plots, and legumes stimulated it. N fertilization overcame this inhibition except in the case of Brachiaria humidicola .     

Short-term kinetics of residual wheat straw C and N under field conditions: characterization by 13C15N tracing and soil particle size fractionation

Summary A clear understanding of the short-term decomposition and fate of crop residues is necessary to predict the availability of mineral N in soil. The fate of ¹³ C¹⁵N-labelled wheat straw in a silty soil (Typic Hapludalf) was studied using particle size fractionation and in situ incubation in which the equivalent of 8 t dry matter per ha of straw was incorporated into the soil over 574 days. Soil samples were separated into five particle-size fractions by wet sieving after disruption of aggregates. The weight, C and N contents, and ¹³C and ¹⁵N atom excess of each fraction were determined. Straw-derived C disappeared rapidly from the > 2000-μm fraction with an estimated half-life of 53 'normalized' days (equivalent of 10°C and −0−01 MPA water potential). Straw-derived C appeared to be only temporarily stored in the intermediate fractions (1000–2000 and 200–1000 pm). The maximum net ¹³C accumulation in the 50–200-μm fraction was 4·4% of added ¹³C. Straw-derived C accumulated most rapidly and preferentially in the 50-μm fraction, which stabilized after 265 days and accounted for 70% of the residual ¹³C on day 574. Although there was more residual ¹⁵N than ¹³C, the distributions and kinetics of the two isotopes in the fractions were similar.     

Nitrogen inputs and outputs in a small agricultural catchment in the eastern part of the United Kingdom

Abstract. Nitrate concentrations measured in an ephemeral stream draining a 170 ha clay catchment in eastern England, with about 23% arable land, were greater than 11.3 mg N 1–¹ on the resumption of flow each autumn but then declined. There was also a spring peak in two years out of seven, 1978–1984, which depend on the length of time soils was at field capacity in the preceding winter. Mean annual load measured in rain was 19 kg N ha^-1 and loss of nitrate in the stream 34 kg N ha^-1. A catchment nitrogen balance suggested that inputs, which averaged 130 kg N ha yr^-1, were generally more than outputs, average 108 kg N ha yr^-1', but gaseous losses were not taken into account.