Mineral Composition and Weathering of Soils Derived from Xiashu Loess

Mineralogical, physical and chemical analyses of the soils derived from Xiashu loess were carried out. The primary minerals of these soils were found to be mainly composed of light minerals, such as quartz, feldspar and mica, with traces of heavy minerals. Clay minerals, more complicate in composition, were dominated by hydromica, accompanied by smectite, vermiculite, chlorite, kaolinite, 2:1/1:1 randomly interstratified minerals and small amounts of quartz, goethite, lepidocrocite and hematite, Clay minerals were characterized by low crystallinity and fine particle size. In light of the quartz/feldspars ratio of the 0.01-0.05mm silt fraction, and the clay mineral composition, the freeness of iron oxide, and the silica/sesquioxide and silica/alumina ratios in < 0.002mm clay fraction, it is concluded that the weathering intensity of these soils was lower than those of red soil and yellow earth, but higher than that of brown earth, and that the soil allitization, depotassication and hydroxylation of cl     

Biotite weathering in podzolic soil under conditions of a model field experiment

The biotite changes in the 1–5 μm fraction after its occurrence in the F, H, AE, and E horizons of a pale-podzolic soil for five years under conditions of a model field experiment were assessed by X-ray diffraction analysis. It was found that the main changes of the biotite in all the horizons included the degradational transformation of its crystal lattice to interstratified mica-vermiculite structures and vermiculite. The intensity of this process gradually decreased from the F horizon down the profile in parallel with the decrease in the amount of roots and the abundance and activity of microbiota. Chloritized structures were present among the products of the biotite weathering in the H, AE, and E horizons; the degree of chloritization gradually increased from the H horizon to the E horizon. The main identified products of the biotite weathering in the AE and E horizons formed during the 5 years of the model experiment were identified in the clay and fine-silt fractions from these horizons of the native pale-podzolic soils. Therefore, the vermiculite, soil chlorite, and mixed-layer illite-vermiculite minerals in the soils studied could be considered as products of the recent soil functioning. The obtained results and literature data showed that the weathering of biotite resulted in the formation of K- and Al-buffer systems.     

Genesis and micromorphology of loess-derived soils from central Kansas

The genesis and micromorphology of three Harney soils from different precipitation regions (from 540 mm to 715 mm) (fine, smectitic, mesic Typic Argiustolls) in the Smoky Hills of central Kansas were investigated. The objectives were to (1) examine the morphological, chemical, physical and mineralogical characteristics of Harney soils formed in loess; (2) determine the clay mineral distribution with depth and the origin of the clay minerals present; and (3) investigate the relationship between the clay mineralogy and other soil properties such as soil plasmic fabric, COLE values and fine clay/total clay ratios. Mineralogical and micromorphological techniques were used to evaluate the characteristics of the loess-derived soils. The first pedon was formed in 88 cm of Bignell loess over Peoria loess and the other two pedons were formed from Peoria loess. The chemical properties were similar for the pedons studied. Differences were observed in physical properties, especially in particle size distribution, oven-dry bulk density and coefficient of linear extensibility values. Although the soils were mapped in the same soil series, the geomorphic positions of the pedons and the nature of the parent material affected the characteristics of the soils. Smectite was the predominant clay mineral, especially in the fine clay fraction, regardless of the location in the precipitation gradient. The dominance of smectite increased in the C-horizons. This implies a detrital source of smectite in the B-horizons formed in both Bignell and Peoria loess units. The presence of randomly interstratified mica-smectite and the micromorphological observations of weathering biotite indicate that weathering also plays an important role in the mineralogy of Harney soils. The high content of clay mica in the surface horizons was caused by dust fall in the study area. Thick and continuous argillans were observed when FC/TC and COLE values were low and crystalline smectite was present. In the lower part of the soil profiles, the plasmic fabric was mostly ma-skelsepic (granostriated b-fabric) and smectite was more crystalline as indicated by sharper X-ray diffraction peaks.     

Biotite weathering in peaty-podzolic gleyic soil under conditions of a model field experiment

Changes in biotite (fraction 1–5 μm) after exposure in the T2, H, Eih, and E horizons of peatypodzolic gleyic soil under conditions of a model field experiment were studied by X-ray diffraction. It was found that the main transformations of the biotite in all horizons included the degradation of its crystal lattice into regularly interstratified biotite-vermiculite and randomly interstratified biotite-smectite structures and vermiculite. The transformation intensity decreased down the profile simultaneously with a reduction in the content of organic matter, roots, and microbiota population and activity. Chloritized structures were also present among the biotite weathering products in the E horizon. The main identified products of biotite weathering formed in horizons Eih and E over a five-year period of the model experiment were detected in the clay and fine silt fractions of these horizons and in native peaty-podzolic gleyic soils. This suggests that vermiculite and soil chlorite in the soils studied are products of soil functioning. It follows from the results, with consideration for literature data, that the weathering of biotite results in the formation of a potassium-buffering system.     

Mineralogical and geo-chemical characterization of a diapiric formation in the North of Spain

We have selected seven profiles located in a diapiric formation in the North of Spain. The profiles have been analyzed for the mineralogy and the chemical composition of original materials, soils developed above them and clay fractions. Three soils formed on basic rock of volcanic origin (ophite) and rich in alterable minerals, three others formed on clay marl and one soil formed on gypsiferous marl. Plagioclases, pyroxenes, vermiculites, and biotites are the main minerals found in the soil samples and ophitic rocks. Biotite, smectite, chlorite and interstratified chlorite–vermiculite make up the predominant mineralogical association in the clay fraction of the soils. Calcite, biotite and on top of all chlorite are the main minerals in the marls and the soils developed on them, with gypsum predominant in the gypsiferous marl. The mineralogy of its clay fraction is comprised mainly of chlorite and biotite. The variations in content of Al₂O₃, TiO₂ and Na₂O in the ophites are considered to be associated with the differences in the evolution of the pyroxenes. The variability of the chemical composition of the Keuper sediments and the soils is attributed more to the chaotic disposition of the Triassic materials in the formation of the diapir than to intense chemical weathering. The low concentrations of silica, iron, and aluminum extractable with ammonium oxalate indicate the low proportion of non-crystalline products. Fundamentally, it is the semiarid conditions in the study zone, together with the processes of extrusion and hydrothermal activity affecting the formation of the diapir, that are responsible for the genesis of the minerals.     

Soil organic matter formation along a chronosequence in the Morteratsch proglacial area (Upper Engadine,Switzerland)

Global warming leads to the melting of ice caps and glaciers and, consequently, the exposure of new areas of land to the atmosphere and weathering. These areas usually have a high reactivity to both biotic and abiotic changes. Proglacial areas in the Alps usually have a deglaciation time span of around 150 years (time since the end of the “Little Ice Age” in the 1850's). We investigated a chronosequence of very young soils in the proglacial area Morteratsch (Swiss Alps) to derive time-trends of soil organic matter accumulation and evolution. Total organic C and N contents, C and N contents of the various organic matter (OM) density fractions and of the labile (oxidised by H₂O₂) and stable (H₂O₂-resistant) fractions were measured. Further characterisation of OM and the various fractions was performed using Diffuse Reflection Infrared Fourier Transform (DRIFT). Soil organic matter has been accumulated over 150 years at very high rates, values lay between 7 and 36 g C/m²/year. This led to a soil organic matter abundance of about 1–5.5 kg C/m² after 140 years. Even at the start of soil formation, a very stable fraction of soil organic matter was detectable. Stable organic matter (resistant to the H₂O₂ treatment) comprised about 6% of the total soil organic carbon and 10% of the total nitrogen. At the start of soil formation, a very high proportion of soil organic matter was present in the density fractions < 1.6 g/cm³. After about 140 years, 15% of soil organic carbon and 35–40% of the nitrogen was already present in the highest density fraction (> 2 g/cm³). With time, the quality of soil organic matter changed: a decrease of hydrophobicity, an increase in aromatic compounds in the bulk soil and a decrease in phenolic functional groups in the heaviest density fraction were detectable with increasing age. In general, stable organic matter as well as the density fraction > 2 g/cm³ had a low C/N ratio and were enriched in proteinaceous materials. The adsorption of proteinaceous materials points to a strong organo-mineral association. This process has existed since the very beginning of soil formation.     

Advances in characterization of soil clay mineralogy using X‐ray diffraction: from decomposition to profile fitting

Structural characterization of soil clay minerals often remains limited despite their key influence on soil properties. In soils, complex clay parageneses result from the coexistence of clay species with contrasting particle sizes and crystal chemistry and from the profusion of mixed layers with variable compositions. The present study aimed to characterize the mineralogy and crystal chemistry of the <2 μm fraction along a profile typical of soils from Western Europe and North America (Neo Luvisol). X‐ray diffraction (XRD) patterns were interpreted using: (i) the combination of XRD pattern decomposition and indirect identification from peak positions commonly applied in soil science; and (ii) the multi‐specimen method. This latter approach implies direct XRD profile fitting and has recently led to significant improvements in the structural characterization of clay minerals in diagenetic and hydrothermal environments. In contrast to the usual approach, the multi‐specimen method allowed the complete structural characterization of complex clay parageneses encountered in soils together with the quantitative analysis of their mineralogy. Throughout the profile, the clay paragenesis of the studied Neo Luvisol systematically includes discrete smectite, illite and kaolinite in addition to randomly interstratified illite‐smectite and chlorite‐smectite. Structural characteristics of the different clay minerals, including the composition of mixed layers, did not vary significantly with depth and are thus indicative of the parent material. The relative proportion of the <2 μm fraction increased with increasing depth simultaneously with smectite relative proportion. These results are consistent with the leaching process described for Luvisols in the literature.     

Weathering of chlorite in a soil derived from a chloritoschist under humid tropical conditions

Eight samples from a soil derived from greenschist were chosen to represent the weathering transformation of chlorite and were subjected to chemical and mineralogical analyses by X-ray, D.T.A., selective and acid dissolution techniques. Regularly interstratified chlorite-vermiculite is the major weathering product in the sand and silt fractions, whereas nontronite predominates in the clay fraction. Kaolinite and a “chlorite-like” mineral progressively appear in the clay fraction as the soil surface is approached. The results show that the genetic link suspected between the clay chloritic component and the kaolinite does not withstand a detailed examination. The clay chloritic mineral is a disordered remnant of the regularly interstratified chlorite-vermiculite and it appears in the clay fraction of the solum concommitantly with the argillitization of the silt fraction. Kaolinite occurs in close association with nontronite and would perhaps form with this mineral a true mixed-layer phase. The unequal distribution of aluminium, iron and magnesium amongst the available sites in the parent chlorite appears to be a factor that strengthens the divergent behaviour of these elements during the weathering.     

辽西褐土的细粒矿物组成

辽宁省西部是低山丘陵区,年平均温度7.1℃,年平均降雨量400—500毫米,降雨集中在夏季,具有明显的大陆性气候特征,干燥度小于1,属半干旱类型.植被为油松柞木和草原灌木丛林.土壤属棕色森林土向栗钙土过渡的褐土地带.母质主要为花岗片麻岩风化物.山麓缓坡和河谷两岸为黄土丘陵.在黄土沉积物覆盖层下,常见红色风化壳露头,即红色粘土层.此外,并有松软易风化岩层,如砂岩、页岩和变质岩等.本区近百年来,由于自然植被受到严重破坏,大量水土流失,土壤侵蚀严重,土壤有机质含量低,成为辽宁省的低产区.因此,鉴定本区不同母质的土壤矿物胶体组成及其特征,不仅可以研究这一特定自然条件下土壤矿物的转化和形成,并且有助于了解土壤特性和肥力特征.     

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.     

Fine silt and clay mineralogical changes of a soil chronosequence in the Langtang valley (Central Nepal)

Chemical and mineralogical properties of a soil chronosequence in the high mountain zone between 3857 m and 4120 m a.s.l. in Central Nepal (Langtang valley) are presented. The soils have been developed in moraine deposits which consist of acid gneisses. They were classified as Entisols, and Spodosols. XRD analyses of the clay and fine silt fraction show increasing changes with distance from the recent Lirung glacier, depending on the time of deposition, resp. soil age. Alteration of illite to interstratified minerals and to hydroxy-Al interlayered minerals or pedogenic chlorite with increasing soil development could be observed. The interstratified minerals could be identified as random and regular illite-interlayered vermiculite mixed-layer minerals. Intensification of the X-ray signals of the fine silt fraction is given compared to the clay. With increasing soil development differences between the clay and fine silt fraction seem to increase. Indications are given of interstratification of the mica-pedogenic chlorite and chloriteinterlayered vermiculite type in the more intensively weathered soils.     

POTASSIUM RESERVES IN A 'HARWELL' SERIES SOIL

A sample of Harwell soil containing 36 percent fine clay (< 0.3 μm) and 14 per cent coarse clay plus fine silt (0.3–5μm) was separated into fractions, and the K-supplying power of soil and fractions measured by cropping with ryegrass, exchange with Ca resin and double-label isotopic exchange with ⁴²K and ⁴⁵Ca ions. Mineralogical examination of the fractions coupled with the cropping experiments showed that the K-supplying power of the soil to ryegrass can be explained by the presence of a zeolite, clinoptilolite-heulandite, in addition to the clay minerals, mica, and interstratified illitic smectite, commonly found in a glauconitic clay-rich soil. The 0.3–5 μm fraction, containing much zeolite, has an exchange diffusion coefficient for K ions to Ca resin of 1.8 × 10^?16 cm²sec^?1 compared with a value of 5.7 × 10^?20 for the < 0.3μm fractions in which interstratified illitic smectite is the dominant mineral. Isotopic exchange shows that all Ca ions in fractions < 50μm are isotopically exchangeable. In fractions coarser than 20μm, some of the K ions in felspar and mica were not exchangeable within the duration of the experiments.     

The nature of smectites and associated interstratified minerals in soils of the Gharb plain of Morocco

The mineralogies of ‘Tirs’ (Typic Pelloxererts), and ‘Debs’ (Typic Haploxerolls and Typic Xerochrepts) soils of the Gharb plain in north-western Morocco are investigated, with special attention given to the determination of the nature of the smectitic phase using the lithium test (Li test) and the alkylammonium method. The sand and silt mineralogy of Tirs soils is dominated by quartz with small amounts of feldspars and kaolinite. The sand and silt fractions of Dehs soils also contain significant amounts of mica, chlorite, and interstratified phyllosilicates. The clay minerals of Tirs soils are predominantly a high-charge smectite. The estimated interlayer charge for this phase is 0.61 mol(c)/O₁₀(OH)₂ and the fraction of tetrahedral charge varies from 38 to 44%. Although the percentage tetrahedral charge is less than 50%, the smectitic phase behaves as beidellite with the Li test. Dehs clays are more heterogeneous, consisting of smectite, vermiculite, illite, kaolinite, chlorite, and interstratified illite/smectite and illite/vermiculite. The Li test and the alkylammonium method demonstrate that a high-charge smectite or vermiculite is interstratified with illite. A low-charge montmorillonite is also present both in Tirs and in Dehs soils. The high-charge beidellitic phase is believed to be a transformation product of mica, whilst the low charge montmorillonite is thought to be inherited from the parent material.     

The influence of weathering processes on labile and stable organic matter in Mediterranean volcanic soils

The relationship and mechanisms among weathering processes, cation fluxes, clay mineralogy, organic matter composition and stability were studied in soils developing on basaltic material in southern Italy (Sicily). The soils were transitions between Phaeozems and Vertisols. Intense losses of the elements Na, Ca and Mg were measured indicating that weathering has occurred over a long period of time. The main weathering processes followed the sequence: amphibole, mica, volcanic glass or if ash was the primary source → smectite → interstratified smectite–kaolinite → kaolinite. Kaolinite formation was strongly related to high Al, Mg and Na losses. The good correlation between oxyhydroxides and kaolinite in the soils suggests that (macro)aggregates have formed due to physical or electrostatic interactions between the 1:1 clay minerals and oxides. The stability of organic matter was investigated with a H₂O₂-treatment that assumes that chemical oxidation mimics the natural oxidative processes. The ratio of C after the H₂O₂ treatment to the total organic C ranged from 1–28%. No correlation between clay content and organic matter (labile or stable fraction) was found. The refractory organic fraction was enriched in aliphatic compounds and did not greatly interact with the kaolinite, smectite or poorly crystalline Fe or Al phases. A part of this fraction (most probably proteins) was bound to crystalline Fe-oxides. In contrast, the oxidisable fraction showed a strong relationship with poorly crystalline oxyhydroxides and kaolinite. Surprisingly, smectite did not contribute to the stabilisation of any of the organic C fractions. The stabilisation of organic matter in the soils has, therefore, two main mechanisms: 1) the protection of labile (oxidisable with H₂O₂) organic matter, including also aromatic-rich compounds such as charcoal, by the formation of aggregates with oxyhydroxides and kaolinite and 2) the formation of a refractory fraction enriched in aliphatic compounds.     

中国土壤颗粒研究 Ⅱ.太湖地区黄泥土型水稻土及其各级颗粒的理化特性

对太湖平原地区高产的黄泥土型水稻土的全土(<1毫米)及7个粒级(1—0.25,0.25—0.05,0.05—0.01,0.01—0.005,0.005—0.002,0.002—0.001和<0.001毫米)共8个土样,进行测定。结果表明:黄泥土粘粒部分(<0.002毫米)的粘土矿物,主要由水云母、高岭和蒙脱组成。粗粘粒级(0.002—0.001毫米)和细粘粒级(<0.001毫米)中粘土矿物的分配有明显差异;砂粒级(1—0.05毫米)中除了主要的石英外,还含有少量“铁锰砂”,所以该粒级中的SiO₂含量较粉粒级(0.05—0.002毫米)的低,而Fe₂O₃的含量则相反,容积磁化率也较高;可塑性和膨胀性都是在<0.002毫米时才始现。上述特点与作者过去所研究的白土型水稻土类似。但是,与国内外报道的几种旱地土壤的资料有所不同。     

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.     

The relationships of the clay mineral suites to the parent rocks of eight soil profiles in Sarawak,Malaysia

The clay mineralogy of eight selected soil profiles developed on acid igneous, pyroclastic and sedimentary rocks was investigated. The effects on the clay mineralogy of the parent-rock mineralogy and physical conditions within each soil profile were evaluated.The results indicate that the mineralogies of the parent rocks control the type of clay minerals formed in Sarawak. In the soils derived from pyroclastic and coarse-grained acid igneous rocks without muscovite, the clay-mineral suites consist almost exclusively of kaolinite and gibbsite with small amounts of goethite. In contrast, in the soils developed from fine-grained acid igneous and sedimentary rocks with muscovite, the clays contain relatively large amounts of interstratified mica-vermiculite and chlorite-vermiculite in addition to gibbsite and/or kaolinite. The presence of gibbsite in these soils depends on the presence of plagioclase feldspar in the parent rock.     

Minerals in the three-component combination of agrochernozems in the Kamennaya Steppe

Properties and mineralogy of fine fractions separated from agrochernozems forming a three-component noncontrasting soil combination in the Kamennaya Steppe have been characterized. The soil cover consists of zooturbated (Haplic Chernozems (Clayic, Aric, Pachic, Calcaric)), migrational-mycelial (Haplic Chernozems (Clayic, Aric, Pachic)), and clay-illuvial (Luvic Chernozems (Clayic, Aric, Pachic)) agrochernozems. All the soils are deeply quasi-gleyed because of periodical groundwater rise. The mineralogy of the fraction <1μm includes irregular mica–smectite interstratifications, di- and trioctahedral hydromicas, imperfect kaolinite, and magnesium–iron chlorite. The profile distribution of these minerals slightly varies depending on the subtype of spot-forming soils. A uniform distribution of clay minerals is observed in zooturbated agrochernozem; a poorly manifested eluvial–illuvial distribution of the smectite phase is observed in the clay-illuvial agrochernozem. The fractions of fine (1–5 μm) and medium (5–10 μm) silt consist of quartz, micas, potassium feldspars, plagioclases, kaolinite, and chlorite. There is no dominant mineral, because the share of each mineral is lower than 35–45%. The silt fractions differ in the quartz-to-mica ratio. The medium silt fraction contains more quartz, and the fine silt fraction contains more micas.     

Landscape evolution in Val Mulix,eastern Swiss Alps – soil chemical and mineralogical analyses as age proxies

Towards the end of the last glacial cycle, repeated re-advances of valley glaciers in the European Alps combined with periglacial processes led to the formation of a variety of climate-related landforms. Independent age measurements of moraines and rock glacier lobes using both in-situ produced and meteoric ¹⁰Be allows for the use of soil formation as an age proxy. In this complementary study we present chemical and mineralogical data from five Podzols from Val Mulix in Eastern Switzerland. Two of them developed on granitic Lateglacial moraines (14.9 ka and 10.7 ka, respectively) and three were sampled on lobes of a morphostratigraphically connected relict rock glacier, covering an age range of approx. 10.7 ka to 8.6 ka. Besides the evaluation of the suitability of selected pedosignatures for a relative age separation, we hypothesised that these pedosignatures should give further information about the evolution of the specific sites. Although the soils had a high skeleton content and the oldest soil started its development in a slightly colder climatic phase, typical weathering trends could still be detected. Whereas weathering indices such as the (K + Ca)/Ti ratio or the B-index reflect time trends reasonably well, the mineralogical composition of the fine earth and clay fraction yielded a slightly more inconsistent picture; to a lesser extent, some inconsistencies were also exhibited when using the weathering mass balance approach. This is especially true for the relict rock glacier and it supports the suggested complex development history of these soils as well as the presence of pre-weathered material. Techniques that include several surface soil horizons and the soil skeleton such as the (K + Ca)/Ti ratio, the B-index and the mass balance approach gave more robust results (in terms of the expected chronology) than the ones that only referred to single horizons (clay mineralogy). Errors or variations due to potential reallocation processes within the soil horizons but without a prominent change of the overall soil characteristics are minimised using such an approach. Weathering indexes and the clay mineral assemblage provided a differentiation of soils even within a relatively narrow time range and gave insight into processes that have occurred at the specific sites. The combined relative-numerical dating approach used here not only enables an extended interpretation and mutual control, but ultimately leads to a better understanding of landscape reconstruction and evolution.     

SANDSTONE-DERIVED SOILS OF A CATENA AT IPERU, NIGERIA

Chemical and mineralogical properties of five soil profiles of a catena in Iperu, Western State of Nigeria, are reported. The pH values of the subsoils are extremely acid. Acidity decreases with improved drainage in the subsoils (pH 4.0–5.8). The cation exchange capacity (C.E.C.) of the soils range from 3.0 to 16.2 me/100g of soil. The silt: silt+clay ratio, calcium: magnesium ratio and Fe₂O₃:Al₂O₃ ratio are used as weathering indices. The low values of the silt: silt + clay index indicate that the soils must have undergone advanced weathering. The magnitude of the Ca: Mg ratio indicates that more calcium than magnesium is available in the soils. The values for sodium and potassium are extremely low. More iron than aluminium was extracted from the soils by the dithionite-citrate method. Kaolinite is the most abundant clay mineral. Halloysite, interstratified clay materials, vermiculite, quartz, and mica are present in considerable amounts. The silt fraction in which quartz is the most abundant mineral, also contain some kaolinite and mica.