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1.
The phosphate fixation capacity at pH 4.5 and an equilibrium concentration of 250 mM phosphate was measured. The soil samples were divided into five groups according to their clay mineralogical composition. The first group soils contain opaline silica and allophanelike constituents, and some unidentified minerals, the second opaline silica and crystalline layer .i1icates, the third opaline silica and crystalline layer silicates with additional allophanelike constituents or aluminarich gel-like materials, the fourth allophanelike constituents, allophane and imogolite and the fifth crystalline layer silicates, allophanelike constituents and alumina-rich gel-like materials, plus some halloysite-like minerals, respectively. The first group soils had phosphate fixation capacities of 3,000 to 8,000, the second group soils 1,000 to 3,000, the third group loib 2,000 to 13,000, the fourth group soils 8,000 to 15,000 and the fifth group soil. 5,000 to 12,000 mg P2O5/100 g oven-dry soil, respectively. The fourth group soils in which allophane and imogolite predominated showed the highest phosphate fixation capacity.

The fractions which dissolved from almost all soil samples by treatments with 6% H2O2 Na2S2O4-NaHCO2-Na citrate and 2% Na2CO3 were estimated to have very high phosphate fixation capacities (8,000 to 19,000 mg P2O5/100 g dry-matter), and there was not much difference among the soil samples examined. Iron and aluminum combined with humus, allophanelike constituents, alumina-rich gel-like materials and halloysite-like minerals in addition to allophane and imogolite contribute to the phosphate fixation of Ando soils.  相似文献   

2.
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.  相似文献   

3.
The clay mineralogy of the Ap horizons of Ando soils in Japanese paddies was determined by a combination of methods and compared with that of Ando soils of uplands. Six of 13 paddy soil samples contained allophane and imogolite and none contained gibbsite, whereas parallel figures were 15 and 7 for 22 upland soil samples. Substantial numbers of diatoms were found in 5 paddy and 1 paddy-converted upland soil samples. The lack of gibbsite was related to the stage of soil formation rather than the paddy condition, whereas the presence of diatoms was related to both. Regarding layer silicates, there was no particular difference between the paddy and upland soil samples but one unidentified mineral with unique morphology and infrared spectrum was found in two paddy soil samples. There was no particular difference in phosphate adsorption between the paddy and upland soil samples.  相似文献   

4.
Abstract

The clay mineralogy of seven Dystrandepts developed on basalts in Northland (New Zealand), the French Massif Central and Western Oregon (U.S.A.) was determined by selective dissolution—differential infrared spectroscopy in combination with chemical, X-ray diffrac tion, electron microscopic and thermogravimetric analyses. Of 14 soil samples, 6 from Northland and Cantal (French Massif Central) contained allophane and imogolite, whereas the remaining 8 did not. Allophane-like constituents and/or “alumina” were found in all the samples, and opaline silica was present in three A1 horizons. The contents of 2 : 1–2 : 1 : 1 layer silicates and their intergrades varied somewhat among the samples. Predominant volcanic glass shards in the Northland Dystrandepts and quartz in the Western Oregon Dystrandepts indicated that their parent materials were not restricted to basalt.  相似文献   

5.
Relationships between the clay mineralogy and the primary mineral association were studied on seventeen Andosol samples (<3,000 years old) collected from Aomori, Hokkaido, and Iwate. Opaline silica, allophane, and imogolite were predominant in the soils derived from volcanic ashes which contained practically no quartz, while opaline silica, crystalline layer silicates, alumina-rich gel-like materials, and allophanelike constituents were abundant in the soils which contained abundant quartz. There was no positive indication of the presence of allophane in any quartz andesitic Andosols. High contents of finely comminuted amphibole and mica in the quartz andesitic volcanic ashes suggested that the crystalline layer silicates are inherited and are not formed pedochemically from amorphous materials.  相似文献   

6.
Abstract

The aluminum solubility of acidified soils both from furrows and under tree canopies of a tea garden was studied using equilibrium experiments in 0.01 mol L?1 CaCl2 solution systems. The soils were originally classified as allophanic Andosols. The furrow soils were more severely acidified because of the heavy application of nitrogen fertilizer, especially in the upper soil horizons (pH[H2O] of 3.6–3.8 in the A1 and 2A2 horizons). These acidified soils were characterized by the dissolution of allophanic materials (allophane, imogolite and allophane-like materials) and by an increase in Al–humus complexes. Ion activity product (IAP) values of the strongly acidified soil horizons were largely undersaturated with respect to imogolite (allophanic clay) or gibbsite. Plots of p(Al3+) as a function of pH strongly indicated that Al solubility of the soils was largely controlled by Al–humus complexes, especially in the A1 horizon. In the canopy soils, which were more weakly acidified (pH[H2O] 4.9–5.0), Al solubility was close to that of gibbsite and allophanic materials, indicating that the solubility is partly controlled by these minerals.  相似文献   

7.
The electric charge characteristics of four Ando soils (A1 and μA1) and a Chernozemic soil (Ap) were studied by measuring retention of NH4+ and Cl at different pH values and NH4Cl concentrations. No positive charge appeared in the Ando soils at pH values 5 to 8.5 except for one containing allophane and imogolite. The magnitude of their negative charge (CEC; meq/l00g soil) was dependent on pH and NH4Cl concentration (C; N) as represented by a regression equation: log CEC =a pH +b log C +c, where the values of a and b were 0.113–0.342 and 0.101–0.315, respectively. Unlike the Chernozemic soil, Ando soils containing allophane, imogolite, and/or 2:1–2:1:1 layer silicate intergrades and humus showed a marked reduction of cation retention as pH decreased from 7 to 5. This was attributed to the charge characteristics of the clay minerals and to the carboxyl groups in humus being blocked by Al and Fe.  相似文献   

8.
9.
Abstract

A method to determine the contents of imogolite and Al-rich allophane (Sil Al ? 1 : 2) in volcanic ash soils was presented. The method is based on the (1) assessment of the presence of Al-rich allophane in clays by successsive extraction with dithionite-citrate and oxalate-oxalic acid, (2) trimethylsilylation of soil clay with a mixture of hexamethyldisiloxane, HCl, and isopropyl alcohol, and determination of the content of monomeric Si based on the trimethylsilyl derivative of monomeric orthosilicate anion by gas / liquid chromatography, (3) determination of the total content of imogolite and Al-rich allophane based on the content of monomeric Si from imogolite, (4) determination of the imogolite content by Thermogravimetry (TG )-Differential Thermal Analysis (DTA) based on the weight loss due to endothermic dehydroxylation with maximum values at ca. 386°C, (5) calculation of the Al-rich allophane content by subtracting the imogolite content from the total content of these minerals, and (6) evaluation of the imogolite and Al-rich allophane content of soil by multiplying clay content of soil and the two mineral content of clay. The trimethylsilylation analysis was found to be reproducible, and the estimated total amounts of two minerals in clays by this method were adequately approximated to those evaluated from the amount of Si (= Sio) extracted with oxalate-oxalic acid after extraction with dithionite-citrate. The variation in the abmldance of two minerals in the soil horizons of volcanic ash soils from the San'in region indicated that this method is suitable for the profile-study of volcanic ash soils.  相似文献   

10.
The mineralogy of the clay fractions separated from the B horizons of two Hydrandepts (Hilo and Akaka soils), a Torrox (Molokai soil) and a Humitropept (Kolekole soil) was determined by a combination of methods.The Hydrandept B horizons were characterized by predominance of hydrous non-crystalline alumina and iron oxides associated with considerable amounts of humus and with very small amounts of silica. Allophane, allophane-like constituents and imogolite were present but in minor amounts. Gibbsite, goethite, chlorite and illite were also present as accessory minerals.The Torrox and Humitropept B horizons were characterized by predominance of kaolinite, hematite and goethite. The iron oxide minerals were present as fine particles (40–80 A diameter) often clustered to form larger aggregates. Neither imogolite nor allophane and allophane-like constituents were detected. Considerable amounts of dithionite-citrate soluble Al and humus were, however, present in the Humitropept B horizon, which may reflect the effect of an admixture of volcanic ash to the parent material.  相似文献   

11.
Thirty-three samples of Ando soils were extracted by sodium pyrophosphate (O.IM; pH 10) and by dithionite-citrate. The Al, Fe, and C contents of these two extracts offer a means of differentiating the status of humus in relation to Al and Fe in the different horizons. The humus that forms at first in the Al horizon has a very low complexing ability for Al and Fe and little is dissolved by pyrophosphate. The humus evolves with time or pedogenesis into forms that complex Al and Fe released from volcanic ash by weathering, and which are dissolved by pyrophosphate. In the old horizons, the humus further reacts with additional Al and Fe, some of which may be present as hydrous oxides or allophane-like constituents, allophane and imogolite. This reaction probably makes the humus less soluble in pyrophosphate.  相似文献   

12.
The nature of amorphous silicates, allophane,ö The name allophane is used in this paper in a dual sense; the one stands for a group of amorphous or nearly amorphous aluminum silicates associated with minor amounts of other metals, and the other in some restricted sense for amorphous silicates other than imogolite. The latter term, imogolite, is used for convenience to denote a component that shows broad x-ray diffractions at 14 (strong), 7.6 (medium) and 5.6 (weak) Å, gives an endotherm at 430°C, and appears as thread-like particles of diameter 100 to 200 Å in electronmicrographs (21). as a main clay constituent determines many of the physical and chemical properties of volcanic ash soils. Recent developments in the study of allophane together with other amorphous inorganic materials in relation to their nature and occurrence in soils have been reviewed by MITCHELL et al. (12).  相似文献   

13.
A contrasting occurrence of clay minerals was found within a soil profile which was derived from volcanic materials in the suburbs of Fukuoka-city, Northern Kyushu. The soil profile is located on an isolated terrace, and the morphological characteristics of the soil correspond exactly to Andosols, so-called Kuroboku soils or Humic Allophane soils.

The clay fraction of upper horizons of the soil consists largely of alumina-rich gel-like materials, gibbsite, and layer silicates such as chlorite and chloritevermiculite intergrades, while that of lower horizons is composed of allophane and gibbsite or halloysite. There was no positive indication of allophane in the upper horizons. Corresponding with the clay mineralogical composition, quartz is abundant in the fine sand fraction of the upper horizons, while the mineral is very scarce or none in the lower horizons, suggesting a close relation between the petrological nature of parent volcanic materials and the mineralogical composition of weathering products. The dominant clay mineral in the volcanic 1.10il might be dependent on the petrological nature of parent materials, and allophane is mostly formed from andesitic materials, and alumina-rich gel-like materials and layer silicates have come from quartz andesitic materials. Allophane would transform to gibbsite or halloysite according to weathering conditions, and aluminarich gel-like materials change to gibbsite under a well-drained condition.

The soil materials have been so greatly weathered that some horizons contain gibbsite of even more than 40 per cent or halloysite over 70 per cent. The morphology and mineralogy are quite similar to so-cailed “non-volcanic Kuroboku soils.”  相似文献   

14.
P. Violante  M.J. Wilson 《Geoderma》1983,29(2):157-174
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.  相似文献   

15.
C.W. Childs  R.L. Parfitt  R. Lee 《Geoderma》1983,29(2):139-155
Chemical and mineralogical data are presented for three Spodosols (podzols) and a related Inceptisol (yellow-brown loam). Allophane with an Al/Si atomic ratio close to two is identified in the B horizons of all four soils, and minor amounts of imogolite are present in association with allophane in all but one soil where small-particle gibbsite occurs. Parent materials for these soils are essentially non-vitric. Allophane (Al/Si = 2) has been estimated quantitatively in all soils using oxalate-extractable Si (Si0) and is selected clay fractions using both Si0 and infrared spectroscopy. Maximum concentrations of allophane (Al/Si = 2) range from 5% to 18% of fine earth (< 2 mm) fractions and all occur in B horizons. Fe0 values are low relative to Al0 values except for the upper horizons of the Inceptisol. Al0 values peak in B horizons and the ratio pyrophosphate-extractable Al to Al0 decreases from about 1 in A and upper B horizons to 0.1–0.4 in lower B horizons.An interpretation of the data is consistent with recent proposals that the movement of Al in podzolisation is due primarily to the formation of inorganic complexes with Si. Chemical criteria for spodic horizons should be consistent with the total illuviation of Al and Fe (and perhaps Si), rather than just the organic-bound fraction of Al and Fe in these horizons as indicated by amounts in extractants such as pyrophosphate.  相似文献   

16.
The transformation of microstructure of constructozems was studied in a four-year-long (2012–2016) field experiment with the use of rheological and electron microscopy methods. Field studies were performed in the area of Moscow State University on three variants of artificial human-made soils (constructozems) differing in the structure of their profiles: (1) the control variant with the upper part composed of a homogenized Ap horizon, (2) the layered constructozem composed of a sequence of layers (Ap–peat–sand–Ap), and (3) the constructozem consisting of a mixture of the above-mentioned horizons. Electron microscopy attested to an increase in differentiation of the pore space in the upper Ap horizons in variants 1 and 2: new pores and chambers of different sizes appeared. In the loose porous mass of the peat layer in variant 2, more compact cohesive microstructures were formed. Microaggregation was identified in the upper layer of variant 3. Changes in the spatial arrangement of the solid phase of the soils were reflected in their rheological properties. A gradual increase in stability of structural bonds in the Ap horizon (variant 1) was detected. In variant 2, the underlying peat layer affected the shape of rheological curves in the Ap horizon. In variant 3, changes in strength properties of the mixed soil mass resulted in the formation of rheological behavior of fluid bodies typical of the plowed humus horizons.  相似文献   

17.
The origin and nature of halloysite in Ando soils from Towada tephra were investigated. These soils were formed from five tephras: Towada-a (1,000 years old), Towada-b (2,000 years old), Chuseri (4,000 years old), Nanbu (8,600 years old) and Ninokura (10,000 years old).Formation of halloysite took place only in the buried soils from Nanbu and Ninokura tephras occurring in an “accumulating zone”, where thicknesses of overburden tephra deposits were mostly 2.5 m or greater and silica enrichment of the clay fractions could occur.The amounts of halloysite were greater in (1) the soils from Ninokura tephra than in those from Nanbu tephra, and greater in (2) the humus horizons as compared to the nonhumus horizons of these same soils. The mean sizes of spheroidal halloysite particles and the ratios of numbers of tubular to spheroidal forms differed with differences in soil horizons and age.High-resolution electron micrographs of glycerol-solvated spheroidal halloysite particles had lattice images of 11 Å due to (001) from the exterior to the interior and had no indications of layer separation. Moreover, the central core of spheroidal halloysite with a diameter of 150 Å showed neither layer structure nor allophane spherules.Results obtained in this study thus indicate that spheroidal and tubular forms of halloysite were formed concurrently in these Ando soils.  相似文献   

18.
Eight samples of Ando soil A1 and buried A1 horizons of different ages were fractionated into clay-, silt-, and sand-size separates, and the yields and carbon contents of these separates were determined. The clay-size separates were subjected to two series of successive extractions, 1) 0.1 M Na4 P2 O7/2% Na2 CO3/0.5 M NaOH and 2) dithionite-citrate/2% Na2 CO3/0.5 M NaOH; and to difference infra-red spectroscopy for identification of the extracted constituents. The result indicated that humus evolves from forms with a very low complexing ability for Al and Fe into forms that complex Al and Fe in the A1 horizon, and that humus further interacts with allophane-like constituents, allophane and imogolite in the buried A1 horizon. These reactions between humus and inorganic constituents result in formation of silt- and sand-size aggregates which are stable to sonic wave treatment, but are broken down into finer particles upon boiling with H2 O2.  相似文献   

19.
Gustafsson et al. in a recent paper in this Journal reported the effects of adding HCl, AlCl3 and Si(OH)4 on the pH and concentrations of Al and Si in 1:1 soil:solution systems at three different temperatures, using samples of soil from an allophanic Bs horizon. Contrary to their conclusions, their observations are compatible with Al in the soil solution being in equilibrium with a proto‐imogolite allophane; it is neither necessary nor even plausible to postulate a hypothetical Al hydroxide. Concentrations of 0.2–0.4 mm Si in the equilibrated solutions at pH 5 could arise from an amorphous silica, probably phytoliths. They cannot come from the allophane.  相似文献   

20.
The role of aluminium on humus accumulation in acid forest soils The impact of soil-borne aluminum on humus accumulation was investigated in a forest soil of the chestnut zone (Castanea sativa) in southern Switzerland (Ticino). Soil samples of two soils formed on bedrocks which differ mainly in their aluminum content were extracted with HNO3, NH4Ac.-EDTA, NH4Cl, KCl, and NH4F-HCl and analyzed for the most abundant elements. On gneiss which contains up to about 10% of total aluminum the common soil type in this area is a Cryptopodzol. This soil is similar to the nonallophanic Udands. It is rich in wellhumified organic matter and shows dark-colored Ah-, A(E)- and Bh-horizons. The soil samples of these horizons are extremely rich in nonexchangeable aluminum which is, however, extractable with NH4Ac.-EDTA. It is assumed that this Al is intimately bound to the organic matter. The soil samples of these horizons contain large amounts of HNO3-extractable phosphorus. Up to 90% of this P appears in the organic fraction. The content of NH4F-HCl-extractable P is only 0.7 to 3.4 mg/kg. It is concluded that due to excessive Al in the organic matter the humus mineralization is inhibited compared to the Haplumbrepts of the region.  相似文献   

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