Amorphous clay materials of towada ando soils

Towada Ando soils consisted of five soils—Towada-a (1,000 years old), Towada-b (2,000 years old), Chuseri (4,000 years old), Nanbu (8,600 years old), and Ninokura soils (10,000 years Amorphous clay materials of these soils taken at different localities were studied by the combined use of selective dissolution and differential infrared spectroscopy, X-ray analysis, electron microscopy, etc.

The main clay minerals of Towada-a soils, present-day soils, were montmorillonite-vermic-ulite chloritic intergrades and opaline silica, or these minerals and allophane in the humus horizons, and allophane in the non-humus ones. Towada-b soils overlain by the Towada-a soils showed the clay mineralogical constituents similar to those of Towada-a soils. However, allophane was one of the main clay minerals in all the humus horizons as well as non-humus ones. The main clay minerals of Chuseri soils were allophane and layer silicates consisting chiefly of chloritic intergrades and chlorite in the humus horizons, and allophane in the non-humus ones. Opaline silica was present in minor amounts in the humus horizons of Chuseri soils, but nearly absent in Nanbu and Ninokura soils.

There were remarkable differences in the clay mineralogical composition of Nanbu and Ninokura soils with differences of their environmental conditions. Allophane and imogolite Were dominant in the clay fractions of both humus and non-humus horizons of very shallowly buried Nanbu soil which was subjected to the strong leaching process. Allophane was the main clay mineral of deeply buried Nanbu and Ninokura soils which showed the absence of notable accumulation of bases and silica. On the contrary, halloysite with a small amount of siliceous amorphous material appeared in very deeply buried Nanbu and Ninokura soils where bases and silica were distinctly accumulated. The amounts of halloysite in the clay fractions were larger in the humus horizons than non-humus ones, and in Ninokura soil than Nanbu soil.

Soil age, soil organic matter, and depositional overburden of tephras were observed to be conspicuous among various factors relating to the weathering of amorphous clay materials in Towada Ando soils.     

The distribution of minor elements among the components of a soil developed in loess

This previously described buried soil, developed in uniform parent material, was used to study the relative movements of elements and other soil components down the profile. Samples from all horizons were treated with hydrogen peroxide and ammonium oxalate, under ultra-violet light, to remove organic matter and sesquioxides, and the residues were subdivided into six particle size fractions.Downward movement of clay (< 0.5 μm) was accompanied by movement of extractable Al₂O₃ and Fe₂O₃, thus identifying these as part of the mobile fraction. The less close relationship of extractable Fe₂O₃ to the clay suggested that it also occurred partly in coarser aggregates. Proportions of minor elements extracted varied from < 1% for Sr to nearly complete extraction of Co, Cu and Mo in some horizons. The extractable fractions of most minor elements throughout the profile behaved more like Fe₂O₃ than Al₂O₃. In the extraction residues, nearly all elements were enriched in the clay fractions relative to the coarser fractions; this being greatest for V and Fe.     

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.     

The origin and early genesis of clay bands in youthful sandy soils along lake Michigan,U.S.A.

A beach ridge and dune complex with good radiocarbon control sampling the last 3500 radiocarbon years B.P. provides new insights on the early genesis of clay bands in sandy soils. Soil profiles were sampled by age groups, described in the field, and then subjected to laboratory analyses for particle-size distribution, pH, organic carbon, carbonate minerals, and extractable iron and manganese. This study suggests that small increases in pH, brought about by small increases in carbonate content within the soil profile, are responsible for flocculating small amounts of illuviated clay. This process, along with a transition to a greater hydraulic conductivity with soil depth due to coarser textures in any given profile, partly explains the existence and possible reason for the initiation of illuvial zones and eventually for clay-band horizons. A pronounced increase in the thickness of incipient clay-band horizons in soils older than 2300 years appears due to finer textures in the parent materials than are present in younger soils. Because of slightly reduced porosity and lower permeability, carbonates and a high pH are retained in both illuvial and eluvial horizons of some of these older soils. In addition, only in those profiles older than 2300 years do clay and iron oxide concentrations coincide and is there some suggestion of greater amounts of extractable manganese in horizons of minimum iron and clay. A pronounced segregation of clay-iron bands is not apparent at the study area but should occur in future years as additional amounts of iron and clay are deposited.     

Effect of Clay Minerals and Organic Matter on the Cation Exchange Capacity of Silt Fractions

The cation exchange capacity (CEC) and specific surface properties were investigated in four particle‐size fractions < 50 μm from three loess (one Kastanozem and two Phaeozems), a holocene (Fluvisol) and a basalt soil (Nitisol) before and after destruction of organic matter. Particle‐size fractions were separated by sedimentation after chemical and physical dispersion of the soil samples. Illite, amorphous minerals, mixed layers, smectite and kaolinite were the predominant clay minerals. They were detected in all size fractions. The CEC increased with increasing organic matter contents and this effect was more pronounced in coarser fractions. The organic matter content per unit surface area was two or three times larger in coarse silt than in clay, irrespective of the soil type.     

The formation of duplex soils on hillslopes in the Sydney Basin,Australia

Field studies of Duplex soils (Red and Yellow Podzolics or Ultisols) on hillslopes in the Sydney Basin show that their primary morphological feature (the texture contrast between A and B horizons) is explicable in terms of differential bedrock alteration combined with downslope movement of the coarser grained materials as a discrete surface layer. The more usually invoked processes of clay illuviation and/or clay destruction are of no more than minor importance in the genesis of Duplex soils in this area.     

Genesis of a Xeralf on feldspathic sandstone, South Australia

A Xeralf on feldspathic sandstone was sampled from a hillslope in the Mount Lofty Ranges in order to study its genesis and, in particular, the origin of the strong texture contrast. Micromorphological study demonstrated that the clay present in void argillans and papules in the B2 horizon accounted for only a small amount of the clay present. Elemental analysis of the whole soil (< 2 mm) and sand, silt and clay fractions showed that there had been considerable weathering of both quartz and microcline, which were the dominant minerals present. Kaolinite is the dominant clay mineral weathering product. Illite appears to be forming from vermiculite in the A horizon. Using zircon as an internal standard, it was shown that elemental losses of SiO₂ and reductions in weight and volume were similar in A and B horizons. Losses of aluminium and potassium were greatest in the A horizon, least in the B3. There has been an absolute increase in the amount of iron. A possible source is iron from heavy mineral bands upslope. It was concluded from the similarity of the quartz particle-size distributions of the A2, B2 and B3 horizons that the intensity of weathering of quartz was the same in A and B horizons. In the case of feldspar (mostly microcline), there is a greater proportion of feldspar in the fine sand and silt fractions of the A2 horizon than in the B horizon. Weathering of feldspar is greatest in the A horizon. The texture profile is principally a function of greater lateral loss of clay from the A horizons compared to the B horizons.     

福建主要土壤的粘粒云母含量和供钾潜力

利用X射线衍射法估算了福建省221个土壤样品中粘粒云母含量并讨论了与粘粒云母含量变化有关的因素。结果表明母质是影响粘粒云母含量的主要因素。海积物、河积物及页岩上发育的土壤粘粒云母含量一般较高;基性岩上发育的土壤粘粒云母含量一般较低。风化度较高的赤红壤、红壤、黄红壤和黄壤等土类的粘粒云母含量一般较低。风化度较低的C层的粘粒云母含量一般较B层和A层高,但异源母质的堆积可以使A层粘粒云母含量高于B层和C层。     

Soil formation in the coast aeolianites and sands of Natal

The morphological, physical, chemical and mineralogical properties of eight prominent classes of soil developed in the coast aeolianites and sands of Natal are presented. These data and information on soil geography lead to the conclusion that: (i) losses of silica and bases and relative accumulation of iron (the ferrallitic process) have given rise to red and yellow kaolinitic materials; (ii) clay eluviation has given rise to coarse textured topsoils and to B2t horizons; and (iii) the hydromorphic process has caused grey colours in many sandy topsoils, plinthite development at some E/B horizon interfaces and gleying of some B2 horizons. In the soils on the older aeolianites, there is no evidence of either podzolization or the coarser textured topsoil being a younger geological deposit. The development of yellow soils in younger aeolianites may indicate a cooler climate than existed when red materials developed from the older aeolianites.     

Properties,weathering and classification of some soils formed in peralkaline volcanic ash in Kenya

Physical, chemical and mineralogical properties were determined for six profiles in and west of the Great Rift Valley in Kenya. Data include morphology, information on gross composition of horizons (organic carbon, cation exchange capacities, extractable cations, etc.), and detailed characterization of the clay fractions by means of transmission electron microscopy, X-ray diffraction, infrared spectroscopy and additional techniques.The three least weathered profiles (Nos. 1–3 of Table I) have morphologies typical of Andepts but lack certain other characteristics common to such soils. Their clay fractions were largely amorphous to X-rays and consisted mainly of poorly ordered siliceous Feoxides with virtually no allophane. All of the clays contained halloysite. The peralkaline nature of the ash parent-material seems responsible for the clay mineralogy of the soils which differs from that generally found in Andepts. The high proportions of iron in the amorphous materials depart from the composition widely reported for such soils. One distinctive feature was the presence of pantelleritic trachyte, found in ash from a number of sites in addition to those of the profiles.How the six profiles may best be classified is an open question. None of the profiles qualifies as Andept. Nor would they be included in the proposed order of Andisols as presently defined. Modifications of the definition of Andisols so as to include some of these soils would seem desirable.     

Fractionation of organo-mineral complexes by sedimentation and density techniques

Soil samples were fractionated by sedimentation in water and by flotation in heavy liquids to separate complexed and uncomplexed organic and inorganic components. Flocculation of clays in heavy organic liquids was delayed by addition of a surfactant. Heavy liquids and surfactants sorbed by soil components were removed by washing with acetone-water mixtures.In a sample of a red-brown earth, the organic carbon and nitrogen contents were highest in the finest separates. In samples of a ground-water rendzina and a chernozemic soil, the coarse clay and silt separates had the highest organic carbon and nitrogen contents. Organic matter was concentrated in low density fractions in all separates. Carbon/nitrogen ratios were lowest in the finer and heavier separates. Calcium, and to a lesser extent manganese, iron and phosphorus, were concentrated in low density fractions: thus these elements appear to be associated with organic matter and may be important in organo-mineral complex formation. Carbonates, titanium, iron, silicon and potassium were concentrated at the highest densities.Organic fractions < 2.06 g cm^?3 from sand size separates were insoluble in alkali and had wide carbon/nitrogen ratios characteristic of plant debris. The light fractions from fine silt and coarse clay separates were more soluble in alkali but showed high ratios of humic to fulvic materials and high absorption at 280 nm. Such materials were considered to be microbial cell debris and were associated with high contents of disordered aluminium and iron oxides and expanding lattice silicates in 1 to 5 μm aggregates.Heavier fractions, particularly of finer clay separates, contained more fulvic and humic materials of a more aliphatic nature than those in < 2.06 g cm^?3 fractions. It is suggested that physical sorption on clay surfaces may be more important in these fractions. Ellite and kaolinite were concentrated in medium density fractions, and contents of some iron oxides and titanium minerals were highest in fractions > 2.06 g cm^?3. Such minerals plus quartz and feldspars were associated with minor amounts of organic matter or possibly were not involved in organo-mineral associations.     

Mineralogy of some Italian andosols with special reference to the origin of the clay fraction

The mineralogy of four Italian Andosols - derived from volcanic material either oversaturated or undersaturated with respect to silica - has been investigated by XRD, EM and IR. The crystalline clay minerals in all four profiles are essentially similar, consisting of abundant halloysite with moderate illite and 14A intergrade material, minor kaolinite and occasional gibbsite. The soils also contain large amounts of imogolite and proto-imogolite allophane. With the exception of illite all these clay minerals are believed to be of pedogenic origin. Halloysite occurs in the dehydrated form in the surface horizons but becomes progressively more hydrated with depth. At depths of > 1.4 m the clay fraction consists almost entirely of fully hydrated halloysite, supporting the suggestion that halloysite forms best in a stagnant moisture regime where there is a depositional overburden acting as a silica source. EM observations show that the halloysite may have spherical morphology and may be intimately associated with gas vesicles in pumice grains where it probably forms by the transformation of allophanic material. It seems likely that dehydrated halloysite slowly converts to poorly crystallized kaolinite in the upper horizons of these profiles. The origin of the 2/1 minerals is more problematical. Illite is probably inherited from mica in the parent material but the 14A intergrade material is so poorly ordered that a pedogenic origin seems more likely than formation by inheritance or by transformation of pre-existing 2/1 silicates.     

Pore‐size distribution and particle arrangement in fragipan and nonfragipan horizons

Fragipan is a widely distributed subsoil horizon that induces severe limitations to plant growth and land use, mainly because of its high bulk density. In this work, we evaluated the pore‐size distribution through the analysis of the cumulative curve of intruded mercury volume in some soils with fragipan horizons. This approach provides information also about the arrangement of particles, thus we compared the results obtained for fragipan and nonfragipan horizons to relate porosity and particle arrangement with the specific physical properties of fragipans. The total volume of intruded mercury did not allow to discriminate between fragipan and nonfragipan horizons. However, from the variation of the pore volume as a function of the radius, two modal classes of pores were found, coarse and fine, respectively. The fine‐pore class arose from the arrangement of clay particles, and its volume was correlated to clay contents (r = 0.787) and to clay packing density (r = –0.621). The clay fractions in fragipans were less densely packed than in the other B horizons, even if they had similar clay contents. The coarser‐pore modal class is known to arise from the interactions between clay, silt, and sand particles, and its volume was different among horizons. Fragipan had a low volume of this modal pore class. In addition, a packing density for the coarser phase of 0.74, corresponding to a rhombohedral packing, was found only in fragipans. Thus, the low permeability and high bulk density of fragipans are linked to specific arrangements of the particles: an open packing of the clay phase is associated to an extremely dense packing of silt and sand. This combination is not present in any other soil horizon.     

Chemistry of pedogenesis in Indo-Gangetic alluvial plains

Five soil pedons–two aquic and two udic Haplustalfs and one petrocalcic Natrustalf–from the Indo-Gangetic alluvial plain of Western Uttar Pradesh were investigated to evaluate the pedogenetic processes. Sand/silt ratios indicate that parent material discontinuities are insignificant. Higher K content and lower SiO₂/R₂O₃ ratios of the non-clay fractions in Bt, rather than in the A, horizons suggest maximum weathering at or near the surface.
An almost linear relationship between decrease in molar SiO₂/R₂O₃ and % increase in clay to about 100cm depth in all the pedons, presence of clay argillans in Bt horizons (where % clay, fine/coarse clay ratio and bulk density values are greatest), all indicate that the development of argillic horizons in these soils was due, at least partly, to lessivage of clay. Fe in clay fractions decreases with depth whilst Al increases, but in the fine earth both increase steadily with depth. This, together with crystalline iron concretions in the lower Bt horizons, suggests that in Haplustalfs these horizons are gaining clay by neoformation/ reorganization of illuviated constituents, especially A1₂O₃.     

Association of the Fungicide Propiconazole with Size Fractionated Material from a Silty Clay Soil – S.E. Norway

Eroded soil material may be an important transporting agent for pesticides that are strongly sorbed to soil. The abilityof the fungicide propiconazole to interact with colloidal andparticulate materials has been studied by means of sorptionand desorption experiments. Size separation of silty clay soilfrom Mørdre, Norway and subsequent characterization showedthat different size fractions of soil possessed different physical and chemical properties and, therefore, different capacity to associate with propiconazole. A large part of the soil organic carbon was associated with coarser material (2–0.02 mm), which also showed higher affinity towards propiconazole than for smaller size fractions (<20 and <2 μm). Similar K _oc values (2306 and 2244) for the size fractions <2 and <20 μm indicate that organic carbon played a dominant role in the sorption of propiconazole. Furthermore, organic carbon associated with these size fractions seemed to have similar properties withrespect to binding of propiconazole. Although, poor in organiccarbon (0.4%), the smallest size fraction (<2 μm) had higher sorption capacity for propiconazole compared to the medium size fraction (<20 μm). Higher sorption for the smallest size fraction (<2 μm) is probably due to higherspecific surface area, cation exchange capacity and content of Fe/Al oxides (free, organically bound and amorphous oxides) than the other size fractions. Results from the desorption experiments indicate that a part of propiconazole associates with sites in the soil material that resist desorption. Fluvialsediments originating from propiconazole treated fields may, therefore, represent potential reservoirs of propiconazole.Treatment with H₂O₂ modified the sorption/desorptioncharacteristics of the soil beyond that which could be expectedsimply by the removal of organic material. The pH values for all the size fractions decreased, and the specific surface areaof the medium sized fraction (<20 μm) increased from 14 to 19 m² g^-1 after the treatment with H₂O₂,probably due to disruption of the aggregate structure. Carrying out fractionation and separation procedures, it is important to be aware of physical and chemical changes that areintroduced during the different steps. An effort should be made to develop fractionation methods that keep the original characteristics of the soil material as intact as possible.     

Implications of clay mineralogy to the weathering and chemistry of AP horizons of ando soils in Japan

The clay mineralogy of 22 samples of the Ap horizons of Ando soils was determined by a combination of methods. Of these samples, 15 did and 7 did not contain allophane and imogolite. Opaline silica was found in 4 samples, whereas aluminum—humus complexes, iron oxides and layer silicates were found in all samples. The presence of allophane and imogolite and the absence of opaline silica in a few Ap horizons was related to mixing of A₁ horizons and subsoils by cultivation and to lower supplies of organic matter relative to the amounts of aluminum released from volcanic ash by weathering. The contents of 2:1 and 2:1:1 layer silicates and their intergrades were larger in soils in which quartz predominated in fine fractions. It was inferred that aluminum bound with humus and in allophane-like constituents, rather than aluminum in allophane and imogolite, is important in reactions with phosphate and fluoride.     

Contribution of separate solid-phase components to the formation of the cation exchange capacity in the main genetic horizons of meadow-chestnut soils

Different types of cation exchange capacity (CEC) and related chemical properties were determined in the main genetic horizons of meadow-chestnut soils in the mesodepressions at the Dzhanybek Research Station of the Institute of Forestry of the Russian Academy of Sciences. In the A horizon, the CEC is mainly due to the organic matter from the clay and coarse fractions, which provides 36% of the soil CEC, and to labile silicates and other clay minerals of the clay fraction. In the Bt horizon, the CEC is mainly provided by the labile minerals of the clay fraction and organic matter of the clay and coarse fractions. The standard soil CEC was found to be significantly higher than the sum of the exchangeable cations in the A horizon and slightly lower than the sum of the exchangeable cations in the Bt and Bca2 horizons. This difference can be related to the fact that the NH₄⁺ ion, which is selectively adsorbed by clay minerals, is used as a displacing cation during the determination of the exchangeable bases, while the Ba²⁺ ion, which is more selectively adsorbed by organic matter, is used during the determination of the standard CEC. In all the genetic horizons, the experimentally determined value of the standard CEC almost coincides with the CEC value obtained by summing the standard CECs of the different particle-size fractions with account for their contents; hence, this parameter is additive in nature.     

中国长江口潮滩湿地土壤重金属含量的时空变化规律及环境指示意义

The environment of estuarine wetlands has been attracting worldwide attention. To study the spatial distribution of pollutants in the tidal flats of the Yangtze Estuary, Southeast China, the Eastern Tidal Flat of Chongming Island (EC) and the Jiuduansha Shoal (JS) of the estuary were selected as the study sites. At each of the two sites, a cross-transect from land to sea was established and topsoil and soil core samples in the cross-transect were collected spatially and seasonally to determine their contents of heavy metals (Cu, Zn, Pb, Cd, Cr, Ni, Mn, and Fe) and grain-size characteristics. The results showed that the heavy metal loads were commonly higher in the soils of nearshore high tidal flats and had a tendency of decreasing from land to sea at both of the study sites. The contents of heavy metals in the soils of the high and medial tidal flats were mostly higher in April and November but lower in July. Corresponding spatial and seasonal variations in grain size of the intertidal soils were also observed at the two study sites. The soils in the nearshore high tidal flats were finer and gradually got coarser seawards; they were relatively finer in April and November but coarser in July. Furthermore, the contents of heavy metals in the intertidal soils of both the sites EC and JS were significantly positively correlated with the clay (<2 μm) and 2-20 μm fractions, but negatively with the sand (>63 μm) and 20-63 μm fractions, which suggested that the heavy metals in the intertidal soils were primarily combined with the fine particulate fraction (<20 μm), especially clay, and hence the spatial and seasonal variations in heavy metals were actually caused by the change of the grain-size characteristics of the intertidal soils due to the different sedimentary environments in the estuary. The results of this study may also contribute to a better understanding of the soil formation and classification in the tidal flats of the Yangtze Estuary.     

降雨条件下分层土壤入渗特性

通过室内模拟降雨入渗试验,研究了粘土、壤土和沙土3种土壤不同分层组合方式对土壤入渗特性的影响。结果表明:垂直入渗条件下,分层土壤入渗特征由土壤分层组合方式决定;分层土壤累计入渗量与湿润锋距离呈线性相关关系;分层土壤入渗过程中,当粗沙覆盖细沙且降雨强度大于下层细沙土稳定入渗率时,湿润锋以上剖面可以达到或接近饱和,当细沙覆盖粗沙且降雨强度大于细沙土稳定入渗率时,湿润锋剖面中,除细沙土部分剖面达到饱和,其余粗沙土剖面无法达到饱和,且其饱和程度和下层粗沙土土壤持水能力有关。     

Extractable Al and Si compounds in pale-podzolic soils of the Central Forest Reserve: Contents and distribution along the profile and by size fractions

The profile distributions of oxalate- and pyrophosphate-soluble Al compounds and oxalate-soluble Si compounds in the main horizons of pale-podzolic soils of the Central Forest Reserve and the fractions <1. 1–5, and >5 μm have been considered. In the clay-eluvial part of soil profile, the content of these compounds is differentiated by the eluvial–illuvial type with a clear accumulation in the EL horizon compared to the AEL horizon. This distribution is largely ensured by their differentiation in the clay and fine silt fractions, while an accumulative distribution of mobile Al compounds is observed in fractions >5 μm. The high correlation between the Al and Si contents in the Tamm extracts from the clay and fine silt fractions with the (Al_ox–Al_py)/Si_ox molar ratios, which are in the range of 1–3 in the EL horizon, confirms that mobile compounds are accumulated in these fractions in the form of amorphous aluminosilicates. In the AEL and EL horizons, an additional amount of Al can pass into the oxalate solution from the fine fractions due to the dissolution of Al hydroxide interlayers of soil chlorites. The eluvial–illuvial distribution of mobile Al and Si compounds typical for Al–Fe–humus podzols within the clay-illuvial part of profiles of the soils under study can be considered as an example of superimposed evolution.