Genesis and dynamics of an oxic dystrochrept and a typic haploperox from ultrabasic rock in the tropical rain forest climate of south-east Brazil

Oxisols are a product of long and intense weathering. Their actual characteristics can neither be traced back to a certain climatic period, nor do they reveal the present soil-forming factors. In this paper, therefore, a reconstruction of the soil genesis of a strongly weathered Oxisol is attempted by comparing the present mineralogical status and the recent dynamics of selected elements with a nearby Inceptisol from the same catena. The parent rock of both soils is serpentinized dunite with nepheline-syenitic veins; the soil moisture regime is udic. Chemical and mineralogical parameters, as well as the concentration of elements in the soil solution of a Typic Haploperox and an Oxic Dystrochrept from the same catena were analyzed for one year. The dynamics of Si and Mg strongly depended on the state of weathering. In the saprolite of the Dystrochrept, Si is partially removed and partially fixed by the formation of quartz and mixed layer minerals. Mg is first fixed in mixed layer minerals, but is during consecutive weathering leached from the transition zone from saprolite to the oxic horizon. Due to the high redox potential, Fe is not soluble, forming goethite in the upper part of the saprolite. Al is also not removed and is finally fixed in kaolinite. In the weathered upper part of both profiles the concentration of Al, Si, Mg and Fe in the soil solution is too low to perceive a further weathering. The present dynamics of Fe, Al, Mg and Si and the mineralogical status of the Dystrochrept indicate that these processes are similar to those that have led to the formation of the Haploperox. The soils, therefore, developed exclusively by the relative enrichment of Al and Fe, the partial loss of Si and the almost complete loss of Mg. Desilification and ‘laterisation’ are hence processes occurring also presently under a tropical rain forest climate.     

Alteration profonde preglaciaire d'un gneiss a Charlesbourg,Quebec (Canada)

A saprolite derived from a gneiss has been sampled in a fault zone at Charlesbourg, near Quebec city. The weathering largely exceeding 6 m in depth and a till overburden suggest preglacial alteration under warmer climatic conditions. This is further supported by the presence of high (up to 15% ) percentages of crystalline iron oxides (goethite and lepidocrocite). Four different facies were defined in the saprolite. Mineralogical analyses were performed on the clay fractions and the following associations were found: swelling minerals + kaolinite, kaolinite, kaolinite + gibbsite, swelling minerals + kaolinite.The degree of weathering of 2:1 minerals into kaolinite seemed to be related to internal drainage conditions. Cation exchange capacity of the saprolite was adequately explained by the clay and silt fraction contributions.     

Inverse models to analyze the spatiotemporal variations of chemical weathering fluxes in a granito-gneissic watershed: Mule Hole, South India

Water-rock reactions are driven by the influx of water, which are out of equilibrium with the mineral assemblage in the rock. Here a mass balance approach is adopted to quantify these reactions. Based on field experiments carried out in a granito-gneissic small experimental watershed (SEW), Mule Hole SEW (~ 4.5 km²), quartz, oligoclase, sericite, epidote and chlorite are identified as the basic primary minerals while kaolinite, goethite and smectite are identified as the secondary minerals. Observed groundwater chemistry is used to determine the weathering rates, in terms of ‘Mass Transfer Coefficients’ (MTCs), of both primary and secondary minerals.Weathering rates for primary and secondary minerals are quantified in two steps. In the first step, top red soil is analyzed considering precipitation chemistry as initial phase and water chemistry of seepage flow as final phase. In the second step, minerals present in the saprolite layer are analyzed considering groundwater chemistry as the output phase. Weathering rates thus obtained are converted into weathering fluxes (Q_weathering) using the recharge quantity.Spatial variability in the mineralogy observed among the thirteen wells of Mule Hole SEW is observed to be reflected in the MTC results and thus in the weathering fluxes. Weathering rates of the minerals in this silicate system varied from few 10 μmol/L (in case of biotite) to 1000 s of micromoles per liter (calcite). Similarly, fluxes of biotite are observed to be least (7 ± 5 mol/ha/yr) while those of calcite are highest (1265 ± 791 mol/ha/yr). Further, the fluxes determined annually for all the minerals are observed to be within the bandwidth of the standard deviation of these fluxes. Variations in these annual fluxes are indicating the variations in the precipitation. Hence, the standard deviation indicated the temporal variations in the fluxes, which might be due to the variations in the annual rainfall. Thus, the methodology adopted defines an inverse way of determining weathering fluxes, which mainly contribute to the groundwater concentration.     

Smectite formation produced by weathering in a coarse granite saprolite in Galicia (NW Spain)

Weathering of a calcalkaline granite was studied in the south of Galicia (NW Spain) where the average annual precipitation is 1400 mm and the average annual temperature is 12°C. The original rock contains perthitic K-feldspars, plagioclases with inclusions of muscovite and opaque minerals, quartz and chloritized biotite, with apatite, zircon, sphene and opaques as accessories. In the saprolite the structure of the rock is preserved, the plagioclases show up to grade 4 weathering and the biotites, between 2 and 3. Weathering in quartz and potassium feldspar crystals is manifested only by fracturing. Biotite changes following the parallel linear model and its weathering products are interstratified biotite–vermiculite and iron oxyhydroxides. The plagioclases change to a microgranular material by pseudomorphic transformation. This material, which substitutes the plagioclase, includes small clearly delimited units which retain zones with the optic characteristics of muscovite. X-ray diffraction analyses of microsamples show that they are formed by 1:1 diocthaedral phyllosilicate, smectite and a small quantity of mica. From these facts we concluded that smectite is formed inside the plagioclase crystals, and probably originates from the inclusions of muscovite contained in these crystals, as it is suggested by the microscopic study which shows the increase in volume which occurs when the crystals of muscovite are transformed.     

An unusual occurrence of probable Pleistocene corestone within a Cretaceous dioritic enclave,Peninsular Ranges,California

We here document an unusual occurrence of probable Pleistocene corestone within an ∼ 5 m by ∼ 5 m dioritic enclave contained within a Cretaceous tonalitic pluton, Santa Margarita Ecological Reserve, SW California. The enclave lies within ∼ 3.5 km of the seismically active ∼ 1.5–2 Ma Elsinore fault zone, and may have been subjected to ∼ 70–90 ground shaking events since ∼ 22,000–18,000 years ago. The studied corestone is elliptical with major axis measuring ∼ 55 cm and minor axis ∼ 26 cm in length. It is surrounded by a discontinuous ∼ 7 cm thick rind that breaks apart under slightly greater finger pressure than does the surrounding saprolite. In order to assess changes in the physical and chemical properties of the corestone, rind, and saprolite we collected along an ∼ 66.5 cm long traverse 4 samples from the corestone, 1 from the rind, and 5 from the saprolite for bulk and grain density, porosity, and major and trace element analyses. Textural and clay mineral data, along with the redistribution of elemental mass, indicate that the weathering of biotite, and to much lesser degrees apatite and the An-rich cores of plagioclase, played critical roles in the production of saprolite especially in a narrow ∼ 20 cm wide zone adjacent to the rind of the corestone. Within this zone bulk densities reach their minimum values, while porosities and positive volume strains reach their maximums. In addition, the maximum loss of K, Fe, Mn, and Ca mass occurred just inside this region, and is paralleled by the highest CIA values and highest additions of Si and Rb mass. In contrast, the masses of Na and Sr are progressively increased and decreased, respectively along the entire sampling traverse while the loss of Mg, Ti, and P mass is episodic with the greatest losses occurring within the narrow zone adjacent to the rind and at the end of the traverse. The above observations indicate that the conversion of biotite to expandable mixed-layered clay minerals, aided by the alteration of the An-rich cores of plagioclase, produced sufficient stress on grain boundaries that a weakening or loss of intercrystalline cohesion occurred. However, unlike the well documented isovolumetric development of saprolite in other areas, at the study site saprolitization was accompanied by a volume expansion. We speculate that repeated ground shaking in response to earthquakes generated in the nearby Elsinore fault zone may be responsible for this difference. Important byproducts of ground shaking would include additional weakening or loss of intercrystalline cohesion, and the production and enhancement of new and older fluid pathways respectively. The fact that the most intensely altered material at the study site lies adjacent to the boundary between the rind and saprolite, suggests that this interface acted to guide fluid flow around the corestone and rind and into the adjacent saprolite where elemental mass was redistributed down various paths leading to the underlying water table. Most of the leached elemental mass was removed from the area of the sampling traverse, but small increases in Si, Rb, and Na mass suggest redistribution of these elements from elevated areas outside the area sampled during this study. The result of the above complex set of processes is a variably porous and chemically altered saprolitic enclave that is still undergoing modification as it adjusts to the vicissitudes of the paralithic environment and continuing ground shaking during earthquakes generated along the Elsinore fault.     

Die Bindungsformen von Si,Mg, Fe,Al, Mn,Cr, Ni und Co in Saprolit und Laterit über Serpentinit,Insel Gebe,Indonesien

Fixation of Si, Mg, Fe, Al, Mn, Cr, Ni and Co in saprolite and laterite above serpentinite - Gebe Island, Indonesia The fixation of various major and trace elements has been studied in a saprolite/laterite profile above serpentinized peridotite. Sequential extraction of < 63 μm fraction shows different types of element fixation in soil: adsorption on mineral surfaces (1), fixation to Mn-oxides (2), bonding to poorly and better crystallized Fe-oxides (3). In the laterite, most of the extractable Si-, Al-, Cr- and Ni-contents are bound to goethitic Fe-hydroxide. The saprolite has considerable amounts of secondary quartz which has been formed during ageing of amorphous silica modifications. Their precipitation is favoured by high Si adsorption capacity of poorly crystallized Fe-hydroxide. In saprolite and laterite Co is bound to Mn-oxides. It can readily be extracted from pure Mn-oxides. In contrast, the intimate association of Mn-oxides to goethite reduces the rate of easily extractable Mn and Co in middle and upper zones of the laterite.     

The epigenetic replacement of kaolinite by hematite in laterite — petrographic evidence and the mechanisms involved

This paper describes the petrographical and mineralogical transformations accompanying the accumulation of iron oxides within the deep mottled layer of a laterite from Burkina Faso. In this layer, the proportions of purple red hematitic spots or nodules which form at the expense of volumes occupied by a soft microporous kaolinite plasma increase as the surface of the soil is approached. The antagonism between hematite and kaolinite was observed at different levels. In all cases, from the border to the core of the hematitic domains, kaolinite experiences corrosion soon followed by complete destruction. At this later stage, hemalite crystals are organized into thin lamellar structures showing clearly the shapes of former kaolinite platelets. A mechanism explaining coincidence of the accumulation of hematite with the destruction of kaolinite is proposed. We postulate that in the deep layers of laterites fed by Fe²⁺ solutions, the protons necessary to dissolve kaolinite are generated by a reaction similar to the oxidation-hydrolysis step of ferrolysis. In the mottled layer of this laterite, therefore, the progressive building up of a high concentration of iron appears to be the result of two closely related processes, i.e., the precipitation of iron oxides from solution and the concommitant dissolution of kaolinite.     

ANDESITE WEATHERING

Petrographic and quantitative mineralogical analyses of two andesites and their saprolite (weathered rock) from the Cascade Range in California reveal a mineral weathering sequence in the rocks related to crystal size and composition and to weathering environment. Both the hypersthene andesite and the olivine andesite studied have been subjected to moderate to intensive leaching by acid solutions percolating through the superjacent soil bodies. Although the two parent rocks differ in chemical and mineralogical composition, their weathering to saprolite has followed a similar progression. During early stages of weathering of both rocks, relatively large hypersthene phenocrysts are most resistant. Following in decreasing order of resistance in both cases are plagioclase phenocrysts and finegrained mafic minerals, olivine, and glassy matrix material. Quartz is relatively stable in the earliest weathering stages, but it decreases rapidly with increased weathering. Free iron oxides and clay increase with increased weathering. Amorphous clay dominates the early weathering stages, but as weathering progresses, kaolin increases relative to amorphous clay.     

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.     

Potassium dynamics of a forest soil developed on a weathered schist regolith

Soils of the humid tropics are poor in available potassium due to intensive weathering and leaching of nutrients. A study was conducted to investigate the mineralogy and potassium supplying capacity of a forest soil developed on a weathered schist regolith. The quantity–intensity (Q/I) approach was used in thisstudy. The schist regolith showed deep weathering and intense leaching throughout the profile, resulting in low cation exchange capacity (CEC) and available K in soil and saprolite layers. The mineralogy of the regolith was dominanted by kaolinite, gibbsite and goethite. Feldspar, mica and mica–smectite minerals were observed in the lower saprolite layers. The Q/I parameters showed that the soils and saprolites were low in K supply power. This observation was attributed to weathering and intense leaching. The free energy values of K replacement (ΔG _r°) also suggest that soils and saprolites of the schist regolith were deficient in K. The Q/I parameters significantly correlated with organic carbon and clay content, CEC, pH and exchangeable K.     

Evaluation of the Clay Fraction in some Danish Soils,Making Use of High-Gradrent Magnetic Separation (HGMS)

Abstract

After removal of the ‘free Fe-oxyhydroxides’, a high-gradient magnetic separation (HGMS) procedure was used to separate the minerals of the clay fraction in soil samples from different horizons of two Alfisols, a Mollisol, an Ultisol and a Spodosol into a magnetic and a non-magnetic fraction. The magnetic fraction constituted 12–19% of the total clay fraction in the Alfisols, 28–35% in the Mollisol, 9–10% in the Ultisol and 11–16% in the Spodosol. X-Ray diffraction (XRD), Mossbauer spectroscopy and total elemental analysis (TEA) were used for the characterization of the different fractions. The CBD-treated magnetic clay contained mainly paramagnetic 2:1 layer silicate clay minerals, including hydroxy-interlayered clay minerals (HICM) high in Fe. The nonmagnetic clay was composed of diamagnetic minerals such as quartz, feldspars, gibbsite, kaolinite and the diamagnetic 2:1 layer silicate clay minerals.     

CH4 flux in an alas ecosystem formed by forest disturbance near Yakutsk,Eastern Siberia,Russia

Abstract

Quartz and mica contents were determined as a function of particle size of soils over quartz and mica-free basalts in northwestern Kyushu and San-in. The contents of both minerals were much higher in the surface soil horizons than in the lower horizons. Quartz particle size distribution (predominantly 2 to 53 μm) and surface morphology (chip or shard, not euhedral) which are similar to those in the north central Pacific pelagic sediments and Hawaiian soils, indicated that quartz is added as aerosolic dust and loess carried by the circumpolar Westerly Winds from Asian semi-arid and arid regions. Close proximity to the eolian sources was deduced by somewhat coarser texture of the present soil quartz. Lower surface soil quartz content, relative to that in the Hawaiian soils was interpreted as indicating a younger landscape age caused by intensive denudation. The covariant relation between the quartz and miea eontents of soils may suggest that at least a portion of the micaceous minerals and quartz in Ando soils of Japan also has a tropospheric origin.     

Development of a mineralogical matrix at the adsorption of polyelectrolytes on soil minerals and soils

The formation of the adsorption layers of polyelectrolytes (PEs) with the development of a mineralogical matrix on the surface of soil minerals and soils (kaolinite, montmorillonite, quartz sand, gray forest soil, and a chernozem) were established on the basis of direct measurements and IR spectroscopy. The differences in the adsorption kinetics of polyacrylamide (PAM) and polyacrylic acid (PAA) were revealed depending on the mineral nature, which were confirmed by the calculated values of the effective adsorption constants. It was found that the limit values of the PAM and PAA adsorption derived from experimental measurements for all the minerals were significantly higher than the values calculated for the formation of a monomolecular layer, which indicated adsorption on the surface of not only separate macromolecules but also secondary PE structures such as packets or fibrils. The IR spectroscopy studies confirmed the differences in the adsorption mechanism of PEs on soil minerals (from physical adsorption to chemisorption with the formation of surface compounds due to polar groups of PEs and surface groups of mineral particles). As a result, a cluster-matrix structure controlling the physicochemical properties of the modified surface was developed on the surface of natural aluminosilicates and soils.     

Investigation of lichens using molecular techniques and associated mineral accumulations on a basaltic flow in a Mediterranean environment

The role of lichens in the breakdown of rocks in various environments is well documented. We investigated the formation of secondary minerals under 13 different fungal species growing on a basaltic flow in Sanliurfa (Turkey) to understand the influence of lichen species on the transformation of minerals in a Mediterranean environment. We used molecular technique (rDNA sequence) to identify 13 different species of lichens (7 crustose, 5 foliose and 1 pathogenic). X-ray diffraction and scanning electron microscopy were used to determine the composition of mineral accumulations. The formation of quartz and 2:1 phyllosilicates in various layers (top, brown and white) of the weathered basaltic flows under all the lichen colonies may be the result of precipitated silica alone (quartz) or in combination with aluminum (2:1 clays) released as a by-product during the breakdown/weathering of primary silicate minerals present in the basalt. However, aeolian deposition may also be a possible source of these mineral species. Whewellite, a calcium oxalate mineral, accumulates in the weathered basalt underneath all the species of lichens. We believe that the formation of whewellite was due to organic acids excreted by fungal hyphae to dissolve primary minerals (e.g., olivine and feldspars); this lichen-mediated process released enough calcium and generated oxalate necessary for the formation of whewellite.     

Mineralogical Composition and Sources of Airborne Settling Particles on Lake Kinneret (the Sea of Galilee), Israel

The dustfall around Lake Kinneret (LK), northernIsrael was collected monthly for four and a half years, January 1993–May 1997. The inorganic waterinsoluble portions were found to be composed mainlyof four non-clay minerals: quartz, feldspars, calciteand dolomite. The principal clay minerals, about 10%of the IWI, were palygorskite, kaolinite, illite andsmectite. A seasonal non-clay mineral distributionvariation was noticed, being richer in quartz in thewinter and richer in carbonates, especially calcite,in the summer. During dust storm episodes the amountof quartz (and also feldspar) in the dustfallincreased markedly. Near basalt and volcanic tuffquarries, the predominant minerals are of the feldspargroup. The origin of the quartz was found to be longrange transport, whilst the other minerals are mainlyof intermediate and local origin.     

Exothermic and endothermic soils of Iceland

This paper is based on the results of the study of soils and soil-forming rocks on five key sites in Iceland, including the coastal plain (the Hvammur key site), piedmont plain (the Hveragerði key site), the Holocene lava plateau (the Reykjanes key site), and the zone of modern hydrothermal activity in the north of the rift zone of Iceland (the Theistareykir and Námafjall key sites). The studied soils are subdivided by us into the groups of exothermic and endothermic soils. Exothermic soils are the soils that develop from the congealed volcanic deposits. These soils are specified by the homogeneous dark gray color and sandy texture. Their mineral components are weakly transformed. Exothermic soils developed under good drainage conditions have the low content of organic matter (about 1.5% C_org). The soil reaction is neutral within the entire profile. Under impeded drainage conditions, the organic carbon content in the exothermic soils reaches its maximum of about 7%, and the soil reaction varies from acid to neutral values. Endothermic soils are the soils that are subjected at present or were subjected in the past to the high-temperature hydrothermal metamorphism. They have mottled color patterns with sharp color contrast in the soil profile; their texture is loamy or clayey. These soils are rich in secondary minerals with a predominance of smectite; kaolinite, pyrite, anatase, gypsum, and other secondary minerals can also be found in them. The properties of endothermic soils are largely controlled by the provincial features of the hydrothermal activity, including the chemical composition of hydrothermal water, the soil temperature, the duration of hydrothermal activity, etc.     

氧化石墨烯和五价砷在改性多孔介质中的共迁移特征

砷是农田土壤重金属污染的主要元素之一,在砷污染农田土壤的修复过程中往往忽视纳米颗粒能够使结合态的砷重新释放,导致有效态砷浓度升高,探究土壤中黏土矿物对氧化石墨烯(Graphene Oxide,GO)和五价砷(As(V))在多孔介质中迁移行为的影响,对进一步完善农田土壤砷修复理论以及提高农作物产量、保护人体健康具有重要意义。该研究利用蒙脱石和高岭石改性石英砂,通过砂柱迁移试验系统地研究了GO、As(V)和GO-As(V)在填加0%、10%、30%和50%的蒙脱石和高岭石改性石英砂柱中的迁移行为。研究结果表明,随着高岭石和蒙脱石改性石英砂填加比例的增加,GO和As(V)的迁移能力均呈降低趋势,且GO和As(V)在不同条件下的迁移曲线均存在显著差异(P0.05);GO在50%高岭石和蒙脱石改性石英砂柱中的回收率相对于石英砂柱分别下降了14%和17%,As(V)分别下降了15%和12%;在共迁移试验中,GO和As(V)在石英砂柱中回收率分别上升至99%和100%。分析表明,As(V)在蒙脱石改性石英砂柱中的迁移能力大于高岭石改性石英砂,而GO与之相反;当GO和与As(V)共迁移时,二者在介质中的迁移能力均大于其单独迁移。本研究表明GO、As(V)释放到土壤后,能够加速As(V)的迁移,造成土壤砷污染的扩大化。     

Micronutrient Contents of a Revegetated Saprolite Exposed by Excavation of an Oxisol

Soils of the Brazilian Cerrado biome have been found to be deficient in copper (Cu) and zinc (Zn). In this area, an Oxisol was deeply excavated in 1962 during the construction of a hydroelectrical plant, and the exposed saprolite material was abandoned, without any reclamation measures. The abandoned land was a harsh environment for plant growth, and the secondary vegetation has not recovered. A field trial was established in 1992 to assess the effects of different grass species and lime amendments on soil reclamation at the degraded site. In 2011 soil samples were collected at three depths (0–10, 10–20, and 20–40 cm) from vegetated and bare plots over tilled saprolite, from an untreated area of the saprolite, and from an Oxisol under native forest, used as external reference. Nineteen years after the reclamation effort was begun, the organic carbon (OC) content of the restored saprolite still was much lower than that of the Oxisol under natural vegetation. The undisturbed Oxisol was deficient in extractable Cu (0.16–0.10 mg kg^?1) and Zn (0.10–0.02 mg kg^?1) and exhibited rather low concentrations of extractable iron (Fe; 5.24–1.47 mg kg^?1) and manganese (Mn; 3.21–0.77 mg kg^?1). However, the saprolite under reclamation showed even lower levels of these elements compared to the native forest soil. In the natural soil, OC, N, extractable Fe, Mn, and Cu showed stratification, but this was not the case for extractable Zn. Although the reclaimed saprolite still was far from predisturbance conditions, the revegetation treatments promoted recovery of OC, N, Fe, Mn, and Cu at the surface layers, which resulted in incipient stratification. Extractable Fe, Mn, and Cu were correlated to OC, whereas no association between Zn and OC was detected. Our results also suggest that reclamation of the excavated saprolite may be constrained by micronutrient deficiencies and mostly by the extremely low levels of Zn and Cu.     

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.     

安徽凤阳石英岩发育土壤的磁学性质及环境磁学意义

通过对安徽凤阳石英岩发育土壤典型剖面的磁学参数测量,结果表明,A层和B层中的磁性矿物含量明显高于C层,且A层和B层中磁性矿物的粒度明显比C层细.C层的磁学性质由磁铁矿主导,A层和B层的磁学性质由磁赤铁矿主导.磁赤铁矿是石英岩在成土过程中形成的次生矿物.土壤中磁赤铁矿的出现及含量的变化指示成土作用的强弱.石英岩的磁性对土壤的磁性影响甚小,而成土作用和生物作用对土壤磁性增强起到了主要作用.