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.     

广西水耕人为土黏粒矿物组成及其空间分布特征

黏粒矿物影响着土壤理化性质,可指示成土因素特征和土壤发生发育过程/强度,也是中国土壤系统分类的基层单元土族矿物学类型划分的重要依据。本研究选择了广西不同纬度和成土母质的18个代表性水耕人为土的剖面,应用X射线衍射(XRD)方法分析了其典型水耕氧化还原层(Br层)的黏粒矿物组成及其空间分布特征,并确定了其中"黏质"剖面的土族控制层段矿物学类型。结果表明:①供试土壤的黏粒矿物主要包括高岭石、伊利石、三水铝石、1.42 nm过渡矿物、蒙脱石和蛭石等,依次分别出现在100%、88.9%、72.2%、61.1%、44.4%和38.9%的剖面中。②黏粒矿物组成在纬度空间分布上具有明显规律性特征。随着纬度降低,土壤黏粒中的高岭石增加,伊利石、蒙脱石、1.42nm过渡矿物逐渐减少;纬度>23°N区域内,成土母质对黏粒矿物组成影响明显。③纬度23°N是黏粒矿物组成和土族矿物学类型分界线,<23°N区域,黏粒矿物均以高岭石为主,是"黏质"剖面的土族控制层段的主要矿物学类型;>23°N区域,黏粒矿物组成以高岭石、蒙脱石、伊利石或1.42 nm过渡矿物为主,因成土母质不同而异,"黏质"剖面的...     

The forms and availability to plants of soil potassium as related to mineralogy for upland Oxisols and Ultisols from Thailand

Potassium (K) deficiency is widespread in crops on highly weathered upland soils under a tropical monsoonal climate. Critical assessment of the forms of K in soils and of the ability of soils to release K for plant uptake is important for the proper management of K in crop production. The relationships between different pools of K were investigated as a function of silt and clay mineralogy for 14 upland Oxisols and 26 upland Ultisols soils from Thailand. Most soils contained no K-minerals in the silt fraction. XRD showed that kaolinite is the dominant clay mineral with variously minor or moderate amounts of illite, hydroxy-Al interlayered vermiculite and smectite present in some soils. For some soils, both conventional and synchrotron XRD were unable to detect illite. Analytical TEM including EFTEM of individual clay crystals showed that clay in the apparently illite-free samples contained very small amounts of illite. Many kaolinite particles appear to contain K which may be present in illite interleaved with kaolinite crystals. A glasshouse K-depletion experiment was conducted to assess the K supply capacity and changes in chemical forms of K and K-minerals using exhaustive K depletion by Guinea grass (Panicum maximum). Potassium deficiency symptoms and mortality of plants occurred on light textured soils, whereas plants survived for six harvests for Oxisols with clay texture, relatively high CEC and higher NH₄OAc-K (exchangeable K plus water-soluble K). There is a strong linear relationship of unit slope between NH₄OAc-K and cumulative K uptake by plants indicating that NH₄OAc-K is a major form of K available to plants. Thus K-bearing minerals contributed little K to plants over the time scale of the experiment and XRD patterns of whole soil samples, silt and clay from soils after cropping mostly showed no change from those for the initial soil. An exception was for a single surface soil clay where a minor amount of smectite was formed from illite by K release to plants.     

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.     

Clay minerals in a soil chronosequence derived from basalt on Hainan Island, China and its implication for pedogenesis

A soil chronosequence consisting of six profiles formed on quartz tholeiite basalt ranging in age from 10,000 years to 1. 8 Million years (My) was studied here. Soil clays were identified using XRD diffractogram decomposition methods for samples obtained from the A and C horizons of profiles. The results showed that kaolinite minerals dominated in all the clay fractions. Gibbsite was prominent in the C horizons in the soils from older rocks. Clays in the A horizon of relatively young soils showed an initial stage of illite formation, followed by smectite mixed layer minerals (illite-smectites and then vermiculite-illite) and finally by vermiculite. The initial presence of illite is interesting as there is no magmatic micaceous or phyllosilicate phase in these basalts and the formation of illite we attribute to a secondary process, probably created by alkali transport by plant materials. The change in 2:1 clay mineralogy reflects the overall change in Si/Al ratios in the soils over longer periods of weathering. In all cases gibbsite is more abundant in the C horizons than the A horizons. The difference in gibbsite content between the A and C horizons we attribute to plant transport of siliceous phytolite material to the surface. Continued high rainfall over long periods of time removed the alkali faster than the plants could bring it to the surface, which led to continuous lowering of 2:1 minerals from younger to older in the soil chronosequence. Nevertheless a 2:1, silica-rich mineral persists in the clay assemblages although in very minor amounts.     

水溶性有机碳在各种粘土底土中的吸附：土壤性质的影响

Clay-rich subsoils are added to sandy soils to improve crop yield and increase organic carbon (C) sequestration; however, little is known about the influence of clay subsoil properties on organic C sorption and desorption. Batch sorption experiments were conducted with nine clay subsoils with a range of properties. The clay subsoils were shaken for 16 h at 4 ^oC with water-extractable organic C (WEOC, 1 224 g C L^-1) from mature wheat residue at a soil to extract ratio of 1:10. After removal of the supernatant, the residual pellet was shaken with deionised water to determine organic C desorption. The WEOC sorption was positively correlated with smectite and illite contents, cation exchange capacity (CEC) and total organic C, but negatively correlated with kaolinite content. Desorption of WEOC expressed as a percentage of WEOC sorbed was negatively correlated with smectite and illite contents, CEC, total and exchangeable calcium (Ca) concentrations and clay content, but positively correlated with kaolinite content. The relative importance of these properties varied among soil types. The soils with a high WEOC sorption capacity had medium CEC and their dominant clay minerals were smectite and illite. In contrast, kaolinite was the dominant clay mineral in the soils with a low WEOC sorption capacity and low-to-medium CEC. However, most soils had properties which could increase WEOC sorption as well as those that could decrease WEOC sorption. The relative importance of properties increasing or decreasing WEOC sorption varied with soils. The soils with high desorption had a low total Ca concentration, low-to-medium CEC and low clay content, whereas the soils with low desorption were characterised by medium-to-high CEC and smectite and illite were the dominant clay minerals. We conclude that WEOC sorption and desorption depend not on a single property but rather a combination of several properties of the subsoils in this study.     

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.     

Transformation of clay minerals in nanoparticles of several zonal soils in China

Purpose

Clay minerals significantly affect the physical, chemical, and biological processes of soils. They undergo spontaneous modification and transformation depending to the climatic conditions. Information concerning the compositions and transformation of clay minerals in nanoparticle colloids (NPs) (25–100 nm) is severely lacking. Studying clay mineral transformation is important approach to understand soil formation. This study was conducted to determine the transformation sequence of clay minerals in several zonal soil NPs.

Materials and methods

Four soils (Haplustalf, Alf-1; Hapludalf, Alf-2; Hapludults, Ult-1 and Ult-2) were collected from B horizons developed under three different climatic zones of China. Alf-1 (36° 05′ N and 117° 24′ E) was located under a warm temperate zone and Alf-2 (30° 38′ N and 115° 26′ E), Ult-1 (29° 13′ N and 113° 46′ E), and Ult-2 (19° 27′ N and 109° 17′ E) under a subtropical zone. The clay particles (<?2000 nm) (CPs) and nanoparticles (25–100 nm) (NPs) of tested soils were separated. The element composition of CPs and NPs was identified by microwave digestion method. The mineralogy and chemical bonding of clay minerals were studied by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR).

Results and discussion

With decreasing latitude, NPs and CPs showed that the molar ratio of SiO₂ to Al₂O₃ trends to diminish, indicating the phenomenon of desilication and allitization in the tested soils. XRD analysis revealed that the main clay mineral of Alf-1 NPs was illite, followed by vermiculite, kaolinite, and kaolinite interstratified minerals (KIMs). The clay minerals of Alf-2, Ult-1, and Ult-2 NPs were dominated by kaolinite (and KIMs), followed by illite, with a little content of hydroxyl-interlayered vermiculite (HIV) in Ult-1 NPs and trace content of gibbsite in Ult-2 NPs. With decreasing latitude, vermiculite and HIV decreased in NPs. When compared to CPs, smectite as well as illite-vermiculite mix-layer mineral (I-V) and illite-HIV mix-layer mineral (I-HIV) were not detected in NPs. The analysis of d060 region by XRD showed that with decreasing latitude, the main clay minerals in NPs were dioctahedral minerals (e.g., illite or kaolinite). These clay minerals resulted from the transformation of trioctahedral minerals in CPs. The disappearance of 2:1 swelling minerals and trioctahedral minerals showed that the NPs were more susceptible to weathering than CPs.

Conclusions

With decreasing latitude, the transformation of clay minerals followed the sequence of illite?→?HIV?→?kaolinite?→?gibbsite in tested NPs.

     

Umwandlungen von Dreischichtsilikaten unter K-Abgabe und K-Aufnahme

Transformation of three-layer silicates through K-release and K-uptake (A review). In soils formed from unconsilidated sediments with illite-vermiculite-smectite mixtures in their clay fractions the clay mineral transformation from illite to vermiculite and smectite between pH 5 and 7 cannot be considered so far as proven on the grounds of available analytical data. Studies of soil profiles showed that the formation of illite from expandable three layer silicates predominates over the formation of smectite from illite. Practically all samples of loess and calcareous tills of the areas discussed contain smectites. K loesses between pH 5 and 7 are probably very small, because K released during the formation of vermiculites from micas is immediately fixed by smectitic layers which are converted to illite. In those soils potential K fixation of the clay fraction (« 2 μ) is lower than in the corresponding parent sediments despite of vermiculite formation in the soils. Further analytical data (X-ray, interlattice-K, K-selectivity, specific surface) support the hypothesis of illitization of smectites during soil formation.     

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.     

Composition of clay minerals and their pedogenetic and taxonomic implications for Stagnic Anthrosols derived from different parent materials in Hunan Province,China

Purpose

The aims of this study were to investigate the composition of clay minerals in soils derived from different parent materials and to elucidate how parent materials and pedogenic environment affect the distribution of clay minerals and reveal the implications for pedogenetics and taxonomy in Stagnic Anthrosols.

Materials and methods

Clay mineralogy and physicochemical properties of the Hydragric horizon of Stagnic Anthrosols derived from granite (GR), plate shale (PS), quaternary red clays (QRC), limestone (LS), purple sandy shale (PSS) and fluvial-lacustrine deposit (FLD) located in Hunan Province of China were analysed to explore the relationships between the conditions influencing the formation of the soil and the composition of clay minerals.

Results and discussion

Results indicated that the composition of clay minerals is closely related to both parent material and type of Stagnic Anthrosols: the soils derived from GR, PS and QRC, which are mostly classified as Fe-accumulic-Stagnic Anthrosols, are dominantly 1:1 type kaolinite and vermiculite and illite/vermiculite mixed layer minerals of widespread distribution. However, soils derived from LS, PSS and FLD were mainly classified as Hapli-Stagnic Anthrosols and are mainly composed of 2:1 type illite/smectite mixed layer minerals, where chlorite is commonly found. Illite is widely distributed and its content varies the least among different parent materials. An extremely significant relationship between pH and kaolinite, chlorite and mixed layer minerals was noted, and the two kinds of mixed layer minerals showed highly significant negative correlation.

Conclusions

This study revealed that the types and quantities of clay minerals in the soil are closely related to the types of parent material. This reflected better direction and degree of development in Stagnic Anthrosols, which is related to the physicochemical properties of parent material and can be used as one of the bases for the classification of soil groups and subgroups within the soil family for Stagnic Anthrosols in Chinese Soil Taxonomy.

     

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.     

Lability of soil organic carbon in tropical soils with different clay minerals

Soil organic carbon (SOC) storage and turnover is influenced by interactions between organic matter and the mineral soil fraction. However, the influence of clay content and type on SOC turnover rates remains unclear, particularly in tropical soils under natural vegetation. We examined the lability of SOC in tropical soils with contrasting clay mineralogy (kaolinite, smectite, allophane and Al-rich chlorite). Soil was sampled from A horizons at six sites in humid tropical areas of Ghana, Malaysian Borneo and the Solomon Islands and separated into fractions above and below 250 μm by wet sieving. Basal soil respiration rates were determined from bulk soils and soil fractions. Substrate induced respiration rates were determined from soil fractions. SOC lability was significantly influenced by clay mineralogy, but not by clay content when compared across contrasting clay minerals. The lability of SOC was lowest in the allophanic and chloritic soil, higher in the kaolinitic soils and highest in the smectitic soil. Our results contrast with conventional concepts of the greater capacity of smectite than of kaolinite to stabilize SOC. Contents of dithionite-citrate-bicarbonate extractable Fe and Al were inversely related to SOC lability when compared across soil types. A stronger inverse correlation between content of ammonium-oxalate extractable Fe and SOC lability was found when considering the kaolinitic soils only and we conclude that the content of active Fe (hydr-) oxides controls SOC stabilization in the kaolinitic soils. Our results suggest that the validity of predictive models of SOC turnover in tropical soils would be improved by the inclusion of soil types and contents of Fe and Al (hydr-) oxides.     

Clay mineralogy in agrochernozems of western Ukraine

The mineralogy of clay fractions separated from deep low-humus deep-gleyic loamy typical agrochernozems on loess-like loams of the Upper Bug and Dniester uplands in the Central Russian loess province of Ukraine consists of complex disordered interstratifications with the segregation of mica- and smectite-type layers (hereafter, smectite phase), tri- and dioctahedral hydromicas, kaolinite, and chlorite. The distribution of the clay fraction is uniform. The proportions of the layered silicates vary significantly within the profile: a decrease in the content of the smectite phase and a relative increase in the content of hydromicas up the soil profile are recorded. In the upper horizons, the contents of kaolinite and chlorite increase, and some amounts of fine quartz, potassium feldspars, and plagioclases are observed. This tendency is observed in agrochernozems developed on the both Upper Bug and Dniester uplands. The differences include the larger amounts of quartz, potassium feldspars, and plagioclases in the clay material of the Upper Bug Upland, while the contents of the smectite phase in the soil profiles of the areas considered are similar. An analogous mineral association is noted in podzolized agrochernozems on loess-like deposits in the Cis-Carpathian region of the Southern Russian loess province developed on the Prut–Dniester and Syan–Dniester uplands. The distribution of particle-size fractions and the mineralogy of the clay fraction indicate the lithogenic heterogeneity of the soil-forming substrate. When the drifts change, the mineral association of the soils developed within the loess-like deposits gives place to minerals dominated by individual smectite with some mica–smectite inter stratifications, hydromicas, and chlorite.     

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.     

Mineralogy and heavy metal contents of soils and stream sediments in a rural region of Western Germany

This paper presents the results of a study of clay mineralogy and Pb, Zn, Cu, Rb, Sr, Y and Zr analyses of soils and stream sediments of the Schwarzach watershed, a drainage system located in a secluded rural region of eastern Bavaria, far removed from major industrial installations.Clay fractions of soils and stream sediments differ significantly in their mineralogy. The soils average 50% secondary chlorite and 40% illite, whereas recent stream sediments average 20% chlorite and 70% illite. These assemblages are possibly interconvertible under the influence, or on withdrawal, of Schwarzach water. Proportions of clay minerals in fossil stream sediments average approximately 30% chlorite, 50% illite, and 20% kaolinite with up to 10% of 10–14 Å interstratified minerals.Surface soil layers have been enriched in Pb, as have recent stream sediments. The latter have also been enriched in Zn and Cu. The increased amounts of Pb plus its close association with organic C indicate atmospheric deposition of Pb and incipient eutrophication of the Schwarzach River.     

南极半岛海洋气候区的土壤Ⅶ. 矿物学特性

南极海洋气候区岩石风化和土壤形成过程中有明显的原生矿物蚀变作用和自生矿物成矿作用。本文以粗骨寒冻灰化土和石灰性扰动冻土两种有代表性的土壤类型为例,阐述了本区土壤矿物学特征。指出铝氧化物、绿泥石、碳酸盐是本区玄武岩类风化物质上发育土壤中的主要自生矿物类型,蒙脱石、特别是绿泥-蒙脱石混层矿物是南极海洋气候区土壤粘粒部分的特征矿物。不同土壤由于成土环境、成土过程、成土历史的差异,其土壤物质的矿物学组成、含量、形态、分布具有明显不同。土壤发生性铁氧化物与成土作用和土壤过程密切相关,其矿物类型、含量、形态特征、分布模式在不同的土壤中明显不同,是表征土壤发育程度与剖面形态表达的有效指标。     

Differentiation of layered silicates and biogenic silica in meadow podbel soils of the Central Amur Lowland

Mineralogy of the fine component of meadow podbel soil in the Central Amur Lowland significantly varies depending on texture differentiation within the profile and clay categories with different binding strengths (water-peptized and aggregated clay). In the eluvial part of the profile, hydromicas are predominant, which are accompanied by kaolinite and mica-smectites with a low content of smectite layers; there are many finely dispersed quartz and feldspars; plagioclases are less abundant. The illuvial part of the profile is characterized by a high content of smectite minerals (mica-smectite and kaolinite-smectite interstratifications). Kaolinite, chlorite, and chlorite-vermiculite are also found. Fragmentary components pass into a peptized state: micas-hydromicas, kaolinite, finely dispersed quartz, feldspars, plagioclases, amphiboles, and diatom skeletons (mainly in the illuvial part of the profile). Aggregated clays are characterized by a high content of interstratifications with smectite layers. The mineral composition of two clay categories is strongly differentiated according to eluvial-illuvial type. The bulk chemical composition confirms the textural differentiation of the finely dispersed component within the profile. The chemistry of silty sand cutans on the faces of structural units in the illuvial part of the profile significantly differs from the chemistry of the enclosing horizon and is analogous to that of the eluvial part of the profile. The involvement of silica in the meadow podbel fractions with different binding strengths has been revealed.     

The effect of seasonal flooding on the clay mineralogy of a soil series in the Volta Lake drawdown area,Ghana

Four pedons of Arenic/Grossarenic Paleustalf (Denteso Series), in the Volta Lake drawdown area in Northern Ghana, were described and sampled just before seasonal floodings commenced in the area. After 5 years of periodic flooding the soils were re-examined and sampled. Soil properties required for soil classification, including the clay mineralogy, of both the pre-flooding and the post-flooding samples were determined. One of the main objectives was to identify changes in soil properties which result from the periodic flooding. X-ray diffraction (XRD) indicated that before flooding the main clay minerals of the Denteso were kaolinite and smectite, and there were also some mica and quartz in the total clay fraction. Comparison of the pre-flooding with the post-flooding data revealed that practically all the smectite disappeared from all the three sampled pedons that were flooded for 5 to 20 weeks during each flood cycle, while the smectite persisted in the non-flooded pedon. With the disappearance of the 2 : 1 lattice clays there occurred a considerable decrease in cation exchange capacity (CEC) and in base saturation of the flooded pedons ranging from 0.04 to 3.63 cmol kg ⁻¹. Also, there was an increase in pH by 0.4 to 1 unit in most horizons of the flooded pedons in spite of the general decrease in base saturation. These changes in CEC, base saturation and pH support the XRD evidence that the seasonal floodings caused pedochemical weathering of the smectite in this loamy sand soil at a very fast rate during the 5 year period and this had resulted in the lowering of the buffering capacity and a general impoverishment of the soil series.     

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.