Effects of silicate weathering and lessivage on K‐content in forest soils derived from Pleistocene sediments

The potassium (K) content of soils developed from Pleistocene calcareous till, glacial sand and loess in NW Germany was investigated in order to characterize stores of K in feldspars (K_feldspar) and mica/illite (K_mica/illite) as well as changes as a function of soil depth. From each horizon, up to seven sand, six silt and three clay fractions were separated. K_feldspar and K_mica/illite were quantified by means of chemical composition and estimation by IR‐spectroscopy. On account of distinct differences in mineralogical composition between different particle size fractions, K‐content of the bulk soil < 2000 μm and the proportion of K_mica/illite and K_feldspar are clearly related to grain size distribution of the sample. Generally, the K‐content of particle size fractions of a soil derived from calcareous till is significantly higher than that of a soil from glacial sands. K_mica/illite of clay and silt fractions increases with depth, reflecting greater mica/illite weathering at the soil surface, whereas K_feldspar shows no noticeable change. Illite accumulates by lessivage in Bt horizons. On a whole‐soil basis, the Bt horizons of Luvisols derived from loess and calcareous till contain more K_mica/illite than either the A or the C horizons. By comparing the K‐content in the different particle size fractions with soil depth, the highest rate of change is found for soils derived from glacial sand. Gains in K in the silt fractions of soils from calcareous till and glacial sand result from weathering of feldspar sand grains. Additionally, decomposition of feldspar‐containing rock fragments of gravel size, and aeolian sedimentation, may also have contributed to these gains.     

Potassium release characteristics and mineralogical characteristics of some delaware soils

Abstract

Twenty‐eight agriculturally important Delaware soils were cropped intensively in a greenhouse experiment. There was no consistent positive correlation between K uptake and percent sand, silt, clay, clay minerals of the clay fraction, K‐feld‐spars of the sand fraction or K‐feldspar weathering of the soils from the A horizon. Only potassium feldspar from the sand fraction and K‐feldspar weathering correlated with K uptake in the soils of the B horizon. This correlation was only significant at the latter part of the experiment when nonexchangeable K was probably the source of plant available K.     

Short‐time clay‐mineral evolution in a soil chronosequence in Oléron Island (France)

Major weathering sequences in soils are well established; however, knowledge on rates of mineral transformations remains unknown, because it is often difficult to date precisely soil processes. This work was carried out on soils developed on recent (< 188 y) sand dunes on the W coast of Oléron Island (France). The coast has been protected against marine and wind erosion by constructing five consecutives barriers close to the coastline since 1820 (1820, 1864, 1876, 1889, 1948) defining the maximum age of the soil parent material, as before the areas between the barriers were under water. Soils on the older dunes have low clay content (> 94% of sand) and exhibit a bleached E horizon that overlies a yellowish brown B horizon. The process responsible for their formation is podzolization promoted by the high permeability of the material and complexing organic matter produced by coniferous vegetation. Initial mineralogy of C horizons is homogenous and constituted of chlorite, illite, illite/smectite mixed‐layer minerals, and kaolinite, quartz, calcite (≈ 8% related to shell fragments), and feldspars. The initial clay‐mineral assemblage of the E horizons is dominated by illite (well‐crystallized WCI and poorly crystallized PCI) and chlorite. With progressive podzolization, poorly crystallized illite is first transformed to illite/smectite mixed‐layer minerals and in a further step into smectite. In addition, transformation of well‐crystallized illite leads to formation of ordered illite/smectite mixed‐layer minerals in the E horizons, which is not commonly described in soils. In the B horizons, illite/smectite mixed‐layer minerals are present with traces of smectite, as well as Al and Fe oxi‐hydroxides as revealed by DCB and oxalate chemical extractions. This chronosequence illustrates that over short distances and short time (< 188 y) intense mineral weathering and soil development occur. Major clay‐mineral changes occur between 132 and 188 y in agreement with development of the pine forest producing acidic litter.     

Dispersion and migration of fine particles in two palygorskite‐containing soils of the Jordan Valley

Migration of different mineral particles within columns of soil‐sand mixtures containing 10 or 20 mass % of soil was investigated by establishing differences in the mineral suite between the ”︁bulk clay” and the ”︁mobile fine material” fractions. The ”︁bulk clay” fractions of all soils contained smectite, palygorskite, kaolinite, quartz, feldspar, and calcite. The soils were saturated with sodium by leaching with NaCl solution, and then leached with distilled water. Clay dispersion and particle migration occurred in the columns. Values of SAR (sodium adsorption ratio) of the effluent decreased with time due to carbonate dissolution. At a certain SAR value, the clays apparently formed aggregates, and as a consequence particle migration stopped in the column. In addition to clay‐sized particles (< 2 μm), very‐fine‐silt‐sized particles (2— 5 μm) were able to migrate in the soil‐sand mixtures, too, and to some extent fine‐silt‐sized particles (5—10 μm) as well. Average size of mobile particles decreases with increase of soil content in the soil‐sand mixtures. The mineralogical composition of the ”︁mobile fine material” changed during the experiment. At the beginning of the experiment, the ”︁mobile fine material” was enriched in the non‐phyllosilicates (especially in calcite, and in some cases in quartz, feldspar and dolomite) and contained low concentrations of phyllosilicates (smectite, palygorskite and kaolinite). At the end of the experiment, the proportion of non‐phyllosilicates decreased, and as a consequence, the proportion of phyllosilicates increased. Among the non‐phyllosilicates, calcite was the most mobile mineral. Among the phyllosilicates, palygorskite was preferentially mobilized in topsoil horizons. In subsoil horizons, on the other hand, kaolinite was preferentially mobilized. This difference was explained by the different nature of carbonates in the topsoil and subsoil horizons. Palygorskite is preferentially occluded within the soil carbonates of lacustrine origin over smectite and kaolinite. These carbonates are present mainly in the subsoil horizons. As a consequence, the presence of these carbonates in the subsoil horizons decreases the migration of mainly palygorskite.     

Response of soil exchangeable and crop potassium concentrations to variable fertilizer and cropping regimes in long-term field experiments on different soil types

Annual potassium (K) balances have been calculated over a 40‐year period for five field experiments located on varying parent materials (from loamy sand to clay) in south and central Sweden. Each experiment consisted of a number of K fertilizer regimes and was divided into two crop rotations, mixed arable/livestock (I) and arable only (II). Annual calculations were based on data for K inputs through manure and fertilizer, and outputs in crop removal. Plots receiving no K fertilizer showed negative K balances which ranged from 30 to 65 kg ha^?1 year^?1 in rotation I, compared with 10–26 kg ha^?1 year^?1 for rotation II. On sandy loam and clay soils, the K yield of nil K plots (rotation I) increased significantly with time during the experimental period indicating increasing release of K from soil minerals, uptake from deeper soil horizons and/or depletion of exchangeable soil K (K_ex). Significant depletion of K_ex in the topsoil was only found in the loamy sand indicating a K supply from internal sources in the sandy loam and clay soils. On silty clay and clay soils, a grass/clover ley K concentration of ～2% (dry weight) was maintained during the 40‐year study period on the nil K plots, but on the sandy loam, loam and loamy sand, herbage concentrations were generally less than 2% K.     

Characterization of expandable layer silicates in humic‐ferralic cambisols (umbrept) derived from biotite and hornblende

Samples from a paired soil type (humic ferralic cambisol) derived from biotite schist (soil group 1) and amphibolite bedrock (soil group 2) were investigated mineralogically and chemically. Soil smectites and vermiculites were analyzed by using the improved n‐alkylammonium method (Lp correction and curve fitting). The soils of group 1 contain small smectite concentrations. The source mineral is a low charged biotite of the silt fraction (2—6 μm) with a mean layer charge of ξ = 0.58 mol per O₁₀(OH)₂. The soil smectite of the clay fraction (< 2 μm) has a mean layer charge of ξ = 0.48 mol per O₁₀(OH)₂ with nearly 100% tetrahedral substitution. The soils of group 2 contain high smectite concentrations. The total charge of these smectites varies between 0.38 and 0.43 mol per O₁₀(OH)₂. The mean value lies between 0.39 and 0.40 mol per O₁₀(OH)2; 20% of the total charge originates from octahedral substitution. Thus, the tetrahedral charge amounts to 0.32 mol per O₁₀(OH)₂. These amphibolite derived smectites have low K selectivity (K_G values of about 5 (mol/l)^—1/2) and do not show an illitization tendency. The soils of group 1 have an extremely high K selectivity (K_G values ≫ 180 (mol/l)^—1/2) when the K‐saturation is < 1.5% of CEC. The increase of K saturation up to 8—15% in the system ”︁natural soil solution versus solid soil” results in a K_G decrease to around 10 (mol/l)^—1/2. This trend can be interpreted as illitization of highly charged smectites with 100% tetrahedral substitution developing to K bearing 1.0 nm minerals.     

Clay mineralogy differs qualitatively in aggregate‐size classes: clay‐mineral‐based evidence for aggregate hierarchy in temperate soils

Clay minerals have a major role in soil aggregation because of their large specific surface area and surface charges, which stimulate interactions with other mineral particles and organic matter. Soils usually contain a mixture of clay minerals with contrasting surface properties. Although these differences should result in different abilities of clay minerals regarding aggregate formation and stabilization, the role of different clay minerals in aggregation has been seldom evaluated. In this study, we took advantage of the intrinsic mineral heterogeneity of a temperate Luvisol to compare the role of clay minerals in aggregation. First, grassland and tilled soil samples were separated in water into aggregate‐size classes based on the aggregate hierarchy model. Then, clay mineralogy and organic C in the aggregate‐size classes were analysed. Interstratified minerals containing swelling phases accumulated in aggregated fractions compared with free clay fractions under the two land‐uses. The accumulation increased with decreasing aggregate size from large macroaggregates (> 500 µm) to microaggregates (50–250 µm). Carbon content and carbon‐to‐nitrogen ratio followed the opposite trend. This fully supports the aggregate hierarchy model, which postulates an increasing importance of mineral reactivity in smaller aggregates than in larger aggregates in which the cohesion relies mostly on physical enmeshment by fungal hyphae or small roots. Consequently, differences in the proportion of the different 2:1 clay minerals in soils can influence their structure development. Further research on the links between clay mineralogy and aggregation can improve our understanding of mechanisms of soil resistance to erosion and organic matter stabilization.     

Influence of Aluminum Hydroxide on Potassium Release from Two Colombian Soils

Abstract

The effect of sesquioxides on the mechanisms of chemical reactions that govern the transformation between exchangeable potassium (Kex) and non‐exchangeable K (Knex) was studied on acid tropical soils from Colombia: Caribia with predominantly 2∶1 clay minerals and High Terrace with predominantly 1∶1 clay minerals and sesquioxides. Illite and vermiculite are the main clay minerals in Caribia followed by kaolinite, gibbsite, and plagioclase, and kaolinite is the major clay mineral in High Terrace followed by hydroxyl‐Al interlayered vermiculite, quartz, and pyrophyllite. The soils have 1.8 and 0.5% of K₂O, respectively. They were used either untreated or prepared by adding AlCl₃ and NaOH, which produced aluminum hydroxide. The soils were percolated continuously with 10 mM NH₄OAc at pH 7.0 and 10 mM CaCl₂ at pH 5.8 for 120 h at 6 mL h^?1 to examine the release of Kex and Knex. In the untreated soils, NH₄ ⁺ and Ca²⁺ released the same amounts of Kex from Caribia, whereas NH₄ ⁺ released about twice as much Kex as Ca²⁺ from High Terrace. This study proposes that the small ionic size of NH₄ ⁺ (0.54 nm) enables it to enter more easily into the K sites at the broken edges of the kaolinite where Ca²⁺ (0.96 nm) cannot have access. As expected for a soil dominated by 2∶1 clay minerals, Ca²⁺ caused Knex to be released from Caribia with no release by NH₄ ⁺. No Knex was released by either ion from High Terrace. After treatment with aluminum hydroxide, K release from the exchangeable fraction was reduced in Caribia due to the blocking of the exchange sites but release of Knex was not affected. The treatment increased the amount of Kex released from the High Terrace soil and the release of Knex remained negligible although with Ca²⁺ the distinction between Kex and Knex was unclear. The increase in Kex was attributed to the initially acidic conditions produced by adding AlCl₃ which may have dissolved interlayered aluminum hydroxide from the vermiculite present, thus exposing trapped K as exchangeable K. The subsequent precipitation of aluminum hydroxide when NaOH was added did not interfere with the release of this K, and so was probably formed mostly on the surface of the dominant kaolinite. Measurement of availability of K by standard methods using NH₄ salts could result in overestimates in High Terrace and this may be a more general shortcoming of the methods in kaolinitic soils.     

中国东南部某些水稻土的矿物学

Limited information is available concerning the mineralogy of paddy soils in the southeastern China. Using chemical methods in conjunction with X-ray diffractometry, we studied the mineral composition of three paddy soils: Jinghua (paddy soil on Quaternary red clay), Fuyang (Hapl-percogenic loamy paddy soil), and Shaoxing (gleyic clayey paddy soil). All the soils contained quartz, mica, vermiculite, chlorite and kaolinite, and the distribution of these minerals varied with soil particle size fractions. The clay fraction of the Fuyang and Shaoxing soils also contained smectite. Although X-ray data did not show the presence of smectite in the Jinghua soil, this mineral was identified by the chemical method, suggesting a transitional property of the mineral in the soil. Hydroxy-Al interlayered minerals were also present in the clay fraction. The amount of smectite in the soils was 31.6 (Shaoxing), 16.5 (Fuyang), and 21.4 (Jinghua) g kg^-1; for vermiculite it was 33.3 (Shaoxing), 16.5 (Fuyang), and 8.5 (Jinghua) g kg^-1. Smectite was only found in the clay fraction. In contrast, amounts of vermiculite in soil particle size fractions were 3.0~11.4 (sand), 2.1~6.0 (coarse silt), 4.6~18.9 (medium silt), 0.9~40.0 (fine silt), and 17.0~108 (clay) g kg^-1. The amount of noncrystalline aluminosilicates in the soils in g kg^-1 decreased in the order: Shaoxing (2.4) > Jinghua (1.9) > Fuyang (1.7). This study has provided useful mineralogical information that is fundamental in future development of management strategies of the soils.     

Dissolved organic matter sorption by mineral constituents of subsoil clay fractions

The retention of dissolved organic matter in soils is mainly attributed to interactions with the clay fraction. Yet, it is unclear to which extent certain clay‐sized soil constituents contribute to the sorption of dissolved organic matter. In order to identify the mineral constituents controlling the sorption of dissolved organic matter, we carried out experiments on bulk samples and differently pretreated clay‐size separates (untreated, organic matter oxidation with H₂O₂, and organic matter oxidation with H₂O₂ + extraction of Al and Fe oxides) from subsoil horizons of four Inceptisols and one Alfisol. The untreated clay separates of the subsoils sorbed 85 to 95% of the dissolved organic matter the whole soil sorbed. The sorption of the clay fraction increased when indigenous organic matter was oxidized by H₂O₂. Subsequent extraction of Al and Fe oxides/hydroxides caused a sharp decrease of the sorption of dissolved organic matter. This indicated that these oxides/hydroxides in the clay fraction were the main sorbents of dissolved organic matter of the investigated soils. Moreover, the coverage of these sorbents with organic matter reduced the amount of binding sites available for further sorption. The non‐expandable layer silicates, which dominated the investigated clay fractions, exhibited a weak sorption of dissolved organic matter. Whole soils and untreated clay fractions favored the sorption of ”︁hydrophobic” dissolved organic matter. The removal of oxides/hydroxides reduced the sorption of the lignin‐derived ”︁hydrophobic” dissolved organic matter onto the remaining layer silicates stronger than that of ”︁hydrophilic” dissolved organic matter.     

Soil Reserves of Potassium: Release and Availability to Lolium perenne in Relation to Clay Minerals in Six Cropland Soils from Eastern China

An 8‐month greenhouse experiment with ryegrass (Lolium perenne L.) examined the relationship between the dynamics of potassium (K) reserves in soil and changes in clay minerals, using X‐ray diffraction. The capacity of soil to release K was consistent with its ability to supply it and was the highest in the soil samples collected from Laiyang (H₁T₂a), Harbin (H₁T₁) and Beibei (H₂T₄), followed by the sample from Jiangyan (H₁T₂b), and the lowest in the samples from Gao'an (H₂T₃a) and Wangcheng (H₂T₃b). Removal of soil K decreases the intensity of reflections for illite and increases that for interstratified clay minerals. The centre of gravity values of the clay fractions was significantly negatively correlated to the depletion of soil K reserves, as ascertained through chemical extraction or through plant action. The quantitative regression equations between the centre of gravity values and the dynamics of soil reserves of K can be used for predicting the release and plant availability of K even without growing a crop. Copyright © 2017 John Wiley & Sons, Ltd.     

Radiocesium interception potential (RIP) of smectite and kaolin reference minerals containing illite (micaceous mineral) as impurity

Cesium-137 (¹³⁷Cs) is strongly adsorbed on clay minerals, especially on illite. The adsorption of Cs⁺ on reference clay minerals, however, has not been fully investigated in relation to the presence of illite. The objective of this study was to clarify the effect of impurities (i.e., illite and vermiculite), present in reference smectite group minerals and kaolin minerals, on the retention of Cs⁺. The clay mineralogy of the reference minerals was characterized by X-ray diffraction (XRD). The radiocesium interception potential (RIP) was measured as an index of the Cs⁺ retention ability of clays. The content of illite in clay was represented by the total potassium (K) content given that illite is a major source of K in the clay fraction. The content of vermiculite in clay was represented by the Cs fixation capacity induced by Cs saturation followed by heating of samples at 110°C. Metabentonite and beidellite gave extremely high RIP values compared with other smectite group minerals, although a peak for illite (at 1.0 nm) was not observed in XRD analysis. The reference smectite and kaolin minerals showed a range of RIP values, even though their RIP values are theoretically zero. The RIP values had a significant positive correlation with the total K content of all the reference clay minerals (r_s = 0.621*). This indicated that the retention ability for ¹³⁷Cs depended more on the content of illite, as impurity, rather than the type of bulk mineral. Hence, the contribution of illite to the magnitude of the RIP was elucidated by the combination of measurement of total K content and XRD analysis.     

粘土矿物中钾的生物活化: Ⅰ. 外生菌根

A pot experiment was Carried out to in vestigate effect of ectomycorrhizal fungi on eucalyptus growth and K bio-mobilization from soils and clay minerals,In the experiment,sands mixed with soil,KCl-satureated vermiculate and mica,respectively,were used to nurse eucalypus seedings which were nonectomycorrhized or ectomycorrhized by an ectomycorrhizal fungus Pisolithus tinctorius strain XL1(Pt XC1) isolated from a forest soil from Xichang,Sichuan Province,China,and a worldwide well-know ectomycorrhial fungus Pioslithus tinctorius strain 2144(Pt 2144) obtained in Australia.More depletion of HCl-souluble K by mycorrhizas from the soil and minerals than nomycorrhizas suggested that mycorrhizas had a great ability to mobilize K present in the interlayer and feldspar.Mycorrhizal seedlings depressed greatly K digested with HF-HClO4 from substrates after consecutive extractions of soils and minerals by water,ammonium acetate and boiling HCl,while nonmycorrhizal seedlings reduced it little if any,shwing that the mycorrhizal seedlings could mobilize and then utilize the structureal K in mineral lattice,Ectomycorrhizal fungi played a very important role not only in promoting the growth of eucalyptus seedlings but also in mobilizing K in soils and minerals.The infection of Pt XC1 led to a better growth of eucalyptus seedlings and more K accumulation in the seedlings than that of Pt 2144.The large differeces in K accumulation by the seedlings might be due to different abilityes of the two ectomycorrhizal fungi to mobilize K in intelayer and lattice pools in the clay minerals.     

Nitrogen distribution and 15N natural abundances in particle size fractions of a long‐term agricultural field experiment

The present study combined a physical fractionation procedure with the determination of the natural abundance of ¹⁵N to investigate the impact of organic manure and mineral fertilizer application, and fallow on changes of N associated with different soil particle size fractions. The long‐term field experiment was conducted since 1956 in Ultuna, Sweden, on an Eutric Cambisol. Nitrogen in bulk soil and in particle size fractions changed significantly since 1956. The N_t concentrations in bulk soil decreased in all treatments not receiving organic materials. Comparing the N contribution of particle‐size fractions to the total N amount revealed the following ranking: silt > clay > fine clay > fine sand > coarse sand. The relative contribution of N in silt sized particles significantly increased from low to high bulk soil N contents, whereas N in clay and fine clay fractions decreased. The C : N ratios of particle size fractions differed considerably more between treatments than C : N ratios in bulk soils. Generally, the C : N ratios decreased from coarse to fine fractions emphasizing the tendency of smaller fractions being more significant as N sink than as C_org sink. ¹⁵N abundances varied more between particle size fractions of single treatments than between bulk soil from differently treated plots. Within treatments we observed differences of up to 7.1 ‰ between particle size fractions. In most cases δ ¹⁵N values increased with decreasing particle sizes. This pattern on average was similar to changes in δ ¹³ C. Our results suggest that silt sized particles acted as medium‐term sink of introduced N and that ¹⁵N abundances in particle size fractions sensitively reflect changes in N status in response to soil management.     

吉林省主要耕作土壤中含钾矿物组成及其与不同形态钾的关系

通过化学分析 ,X-射线衍射及镜检法研究了黑土、白浆土、黑钙土等吉林省主要耕作土壤的含钾矿物组成及不同形态钾的含量。结果表明 ,土壤中的含钾矿物以含钾长石和伊利石为主 ,钾长石主要集中在土壤砂粒部分 ,伊利石主要存在于土壤的粘粒部分。土壤的含钾矿物总量约占土壤矿物总量的 1/ 3多些 ,比南方土壤高 ;缓效钾含量丰富 ,供钾潜力大 ;速效钾含量在黑土、黑钙土中较高 ,而在白浆土中稍低。 3种土壤的全钾量与含钾矿物总量、粘粒中伊利石含量与粘粒含钾量、伊利石含量与缓效钾量、细砂中含钾长石含量与细砂中全钾量、缓效性钾与速效性钾之间呈极显著或显著相关。     

Clay mineralogical and ammonium fixation characteristics of some tropical upland rice soils

Abstract

In view of the agronomic and economic significance of NH₄ fixation in soils, an attempt has been made to relate this to the most reactive mineral constituents of soils ‐ the clay minerals, under the temperature‐moisture regimes normal to tropical upland rice soils. Laboratory fixation study was done with NH₄, concentrations similar to those common in soils upon N fertilization, and under alternate wetting and drying at ambient temperatures rather than at 100°C as in many published studies.

Results of the investigation show that soil clays with dominant vermiculite and montmorillonite fix the greatest proportion of applied NH₄ (94 and 91%), followed by beidellite (72%) and x‐ray amorphous (45–64%) clays. Fixation is negligible (10%) in the clay with mineral suite consisting of hydrous mica, halloysite, and chlorite. Crystallinity of minerals seems to influence NH₄ fixation appreciably.     

Organic‐carbon fractions in an agricultural topsoil assessed by the determination of the soil mineral surface area

According to recent conceptual models, the organic carbon (OC) of soils can be divided into OC fractions of increasing stability from labile free OC to resistant OC associated with the soil mineral phase. In this study, we present a method for quantifying two OC fractions based on soil aggregate–size fractionation and the N₂ gas–adsorption method. For this purpose, we analyzed soil material of the plow layer of a Haplic Chernozem subjected to different fertilizer treatments (no fertilizer, mineral fertilizer, mineral and organic fertilizer). The total organic‐C concentration (TOC) and the clay content of the different size fractions were determined as well as the specific surface area (SSA_mineral) and the sample pore volume after thermal oxidation (OC‐free). The TOC of the different soil‐aggregate fractions was linearly related to SSA_mineral. Clay‐associated OC and nonassociated OC fractions of the different soil samples were quantified using two methods based on the OC surface loading at the clay fraction. The application of organic fertilizer increased the amount of nonassociated OC but hardly affected the concentration of clay‐associated OC. This finding agrees with previous studies on C dynamics in soils and indicates a finite capacity of soil materials to sequester OC. Even without any addition of organic fertilizer, the mineral phase of the analyzed soil material appears to be C‐saturated.     

Mineralogic evolution in hydromorphic sandy soils and podzols in “landes du médoc”, France

Soils of the nearly level “Landes du Médoc” in southwestern France have a pattern of alternating bodies of hydromorphic podzols (Haplaquods) and low humic hydromorphic soils (Psammaquents). The soils are formed in a sedimentary mantle of coarse, quartzose sands with a slight microrelief consisting of low, elongated ridges and shallow, intervening troughs. The water table is at shallow depths throughout the plain, even at the surface in places. The podzols on the crests of the low ridges have distinct A₂ and cemented B₂ h horizons. Podzols persist down the sides of ridges but going downslope first lose the A₂ horizon and then the cementation of the Bh horizon. Soils in the shallow troughs have A₁ and Cg horizons without B horizons.The fine silt (2–20 μm) and clay (0–2 μm) fractions of the parent sand contain primary trioctahedral chlorite, mica, feldspars, and quartz, with the last mineral predominant. During soil development, the first three minerals undergo weathering at different rates and to different extents. Chlorite is most strongly weathered, followed in order by plagioclases and K-minerals. In the fine silt fraction, weathering seems to occur mostly by fragmentation of particles. In the clay fraction, the phyllosilicates successively form irregularly interstratified minerals with contractible but not expandable vermiculitic layers, interstratified minerals with contractible and expandable smectitic layers, and finally smectites.The extent to which the silicate minerals are weathered becomes progressively greater from the low humic hydromorphic soils to the podzols with friable Bh horizons to the podzols with cemented Bh horizons. Smectite is present only in the A₂ horizons of these last podzols.The aluminum release by weathering of silicate minerals is translocated in part in the form of organo-metal complexes into the Bh horizons of the podzols. Greatest concentrations of Al are associated with coatings of monomorphic organic matter on mineral grains in the cemented Bh horizons, in which some Al has also crystallized into gibbsite. That mineral was not detected in friable B horizons of podzols nor in the low humic hydromorphic soil. Contrary to expectations, the mobile Al did not enter interlayer spaces of expanding 2:1 clay minerals.     

Spatial distribution of clay minerals in agrochernozems of erosional and denudational plains in the Stavropol region

The distribution pattern of the fine fractions (<1.0 and 1?C5 ??m) and the mineralogical composition of the agrochernozems formed on the erosional-denudational plains of the Stavropol region have been studied. Erosion and denudation caused the redistribution of the fine material within the catena with its maximal accumulation on the lowermost part of the slope. The same processes favored the formation of surface deposits slightly differing in the composition of the principal mineral phases, i.e., complex disordered mixedlayered micas-smectites with varying combinations of micaceous and smectite layers in crystallites and di- and trioctahedral hydromicas. Imperfect kaolinite and magnesium-ferric chlorite are accompanying minerals. An increase in the amount of mixed-layered minerals with smectite layer is observed down the profile. In addition to the mentioned minerals, the individual smectite and clinoptilolite, which are components of Tertiary deposits, are identified in the lower parts of the agrochernozem profiles. The fine-silt fractions consist of (in decreasing order) di- and tri-octahedral micas, quartz, feldspars, plagioclase, and an admixture of phyllosilicates (kaolinite, chlorite, and mixed-layered chlorite-smectites). The maximal amount of the fine fraction, as well as the maximal amount of mica in it, is registered in the soils in the lower part of the slope. The phyllosilicates are decomposed in this fraction in the upper horizons. The seven-year-long application of mineral fertilizers intensified the peptization of the soil mass in the arable horizons, which increased the content of clay particles in them. A more contrasting distribution of the mixed-layered formations in the profiles, a considerable decrease in their reflection intensities, an increase in the structural disorder of the minerals, and a certain increase in the content of the fine-dispersed quartz are observed.     

Exploitation of potassium by various crop species from primary minerals in soils rich in micas

We investigated the question of whether exchangeable K⁺ is a reliable factor for K⁺ availability to plants on representative arable soils (Aridisols) rich in K⁺-bearing minerals. Five soils with different textures were collected from different locations in Pakistan and used for pot experiments. The soils were separated into sand, silt, and clay fractions and quartz sand was added to each fraction to bring it to 1 kg per kg whole soil, i.e., for each fraction the quartz sand replaced the weight of the two excluded fractions. On these soil fraction-quartz mixtures wheat, elephant grass, maize, and barley were cultivated in a rotational sequence. Growth on the sand mixture was very poor and except for the elephant grass all species showed severe K⁺-deficiency symptoms. Growth on the mixture with silt and clay fractions was much better than on the sand fraction; there was no major difference in growth and K⁺ supply to plants whether grown on silt or clay, although the clay fraction was rich and the silt fraction poor in exchangeable K⁺. On both these fractions the plant-available K⁺ supply was suboptimal and the plants showed deficiency symptoms except for the elephant grass. This plant species had a relatively low growth rate but it grew similarly on sand, silt, and clay and did not show any K⁺ deficiency symptoms, with the K⁺ concentration in the plant tops indicating a sufficient K⁺ supply regardless of which soil fraction the plants were grown in. The reason for this finding is not yet understood and needs further investigation. It is concluded that on soils rich in mica, exchangeable K⁺ alone is a poor indicator of K⁺ availability to plants and that mica concentrations in the silt and clay fraction are of greater importance in supplying crops with K⁺ than exchangeable K⁺.