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1.
A frayed edge site can be a significant indicator of alterations in illitic minerals in soils evolving under different climates, because illitic minerals are known to enlarge the frayed edge site through vermiculitization. We investigated the relative abundance of this site in soil clays (<2 μm) using Radiocaesium Interception Potential (RIP) methodology, and determined the mineralogical factors controlling its amount (represented by RIP) for soils under ustic soil moisture regimes (northern Thailand, TH) and udic regimes (southwestern Japan, JP; East Kalimantan in Indonesia, ID) in humid Asia. We found three different correlations between RIP and mineralogical- or chemical-indices: positive (amount of illitic mineral and Cs-fixing capacity), negative (amount of kaolinite and hot-citrate extractable Al-Si) and no correlation (amount of DCB-oxides). The variable that correlated best with the logarithm of RIP in each region was Alcit-Sicit (JP), amount of illitic mineral (TH) and amount of kaolinite (ID). Under an ustic soil moisture regime in TH, there was little vermiculitization, as was evidenced by the direct correlation between the frayed edge site (or RIP) and the amount of illitic minerals and the very small Cs-fixing capacity. A distinct dry season restricts water leaching, which may reduce alteration in illitic minerals. For ID soils under an udic soil moisture regime, illitic minerals weather to form vermiculite, which is reflected in the enlargement of the frayed edge site. However, for JP soils, hydroxy-Al interlayering reduces the frayed edge site formed through vermiculitization. The release of hydroxy-Al polymers from vermiculitic layers can induce the re-exposure of the frayed edge site that can be progressive under a podzolization process.  相似文献   

2.
Radiocaesium fixation in soils is reported to occur on frayed edge sites of micaceous minerals. The weathering of mica in acid soils may therefore influence the Cs+ fixation process and thereby the mobility of the radiopollutant. We produced a laboratory weathering model biotite → trioctahedral vermiculite → oxidized vermiculite → hydroxy interlayered vermiculite (HIV) and quantified the Cs+ fixation of each mineral both in a fixed K+–Ca2+ background and in acid conditions. The transformation process was achieved through K depletion by Na-tetraphenylboron, oxidation with Br2 and Al-intercalation using NaOH and AlCl3. In a constant K+–Ca2+ background, vermiculite fixed 92–95% of the initial 137Cs+ contamination while biotite and HIV fixed only 18–33%. In acid conditions, the interlayer occupancy by either potassium (biotite) or hydroxy-Al groups (HIV) strongly limited Cs+ fixation to 1–4% of the initial 137Cs+ contamination. Cs+ fixation occurred on vermiculitic sites associated with micaceous wedge zones. Though both oxidized and trioctahedral vermiculites fixed similar Cs+ amounts in a constant K+–Ca2+ background (92–95%), the oxidized vermiculite retained much more radiocaesium in acid conditions (78–84% against 54–59%), because of its dioctahedral character.  相似文献   

3.
The OAh and Ah horizons of acid brown and podzolic forest soils are reported to fix more radiocaesium than the mineral B horizons beneath them. We determined the respective influence of organic matter and clay minerals on the magnitude of Cs+ retention in a strongly acid brown forest soil in Belgium. The soil contained mica throughout the profile. Vermiculite was identified in the OAh and Ah horizons, and hydroxy interlayered vermiculite (HIV) in the Bw horizon. The OAh and Ah clay fraction retained much more Cs+ than the Bw horizon. The extraction of Al interlayers by Na-citrate resulted in a marked increase in Cs+ fixation in the Bw clays as well as the collapse of the vermiculitic layers after K+ saturation. Organic matter had a strong but indirect effect on Cs+ fixation. In the Bw horizon, acid weathering of layer silicates releases free Al and produces HIV minerals in which Al polymers block the access of radiocaesium onto Cs+-specific sites. In OAh and Ah horizons, free Al is complexed by organic acids. Consequently, the interlayer specific sites remain accessible for Cs+ fixation.  相似文献   

4.
The magnitude of radiocaesium fixation by micaceous clay minerals is affected by their transformation, which depends on weathering in soil. The net retention of radiocaesium traces was quantified by sorption–desorption experiments in the various horizons of four sandy soils forming an acid brown earth–podzol weathering sequence derived from sandy sediments and characterized by marked changes in mineral composition. The features of the 2:1 minerals of the four soils, resulting from an aluminization process in depth and a desaluminization process towards the surface, had a strong influence on Cs+ fixation. Beneath the desaluminization front, which deepens from the acid brown earth to the podzol, hydroxy interlayered vermiculite was dominant and the 137Cs+ fixation was the weakest. At the desaluminization front depth, vermiculite was responsible for the strongest 137Cs+ fixation. In the upper layers, smectite appeared in the podzolized soils and the 137Cs+ fixation decreased. The magnitude in Cs+ fixation therefore appeared as a tracer of the transformation process affecting the 2:1 clay minerals in the acid brown earth–podzol weathering sequence. This magnitude was positively correlated with the vermiculite content of the studied soil materials estimated by the rubidium saturation method.  相似文献   

5.
Background, Aims, and Scope  Hydroxy interlayered vermiculite (HIV) and vermiculite are commonly referred to as 1.4 nm minerals. In the subtropical soils of central China, the concentration of vermiculites decreased while that of HIVs increased gradually from north to south as the intensity of soil formation or eluviation increases in the same direction. The cutans in these soils closely interact with air, roots, microbes, water and dissolved ions in soils. Cutans may therefore be expected to exert an important influence on the formation of 1.4 nm minerals relative to the matrix soils. However, little is known about the transformation of 1.4 nm minerals in Alfisols in central China. Here, we investigate the compositional differences of 1.4 nm minerals in cutans and matrix soils, and the probable transformation of vermiculite to HIV or vice versa when sodium citrate and sodium acetate are added to matrix Alfisols. Methods  Cutans and matrix soils were separated from three soils in the northern subtropical zone in China. The samples were analyzed for Fe, Mn, exchangeable cations, organic matter(O.M.), pH, and clay minerals. To 10 mL of matrix soil, suspensions containing about 250 mg (oven-dry weight) of clay was added with 5 mL of 0.4 mol/dm3 or 2 mol/dm3 of sodium citrate or sodium acetate solution and 5 mL of 0.2 mol/dm3 mixed solutions of CaCl2, Mg(NO3)2 and KCl. After its pH was adjusted to 6.0, the mixture was ‘incubated’ for 120 or 210 days (more than one season or half a year) during which period it was shaken for 1 hour every day. The clay mineral composition of the samples was determined after incubation. Results  Both vermiculites and HIVs were present in matrix soils, but only vermiculties were detected in cutans. The addition of organic ligands (citrate and acetate) promoted the transformation of HIV to vermiculite. This transformation was obvious for the matrix soils that had been incubated with 0.5 mol/dm3 sodium citrate for 210 days while sodium acetate was less effective in this regard. The promoting effect of organic ligands is dependent on type and concentration as well as incubation time. This would suggest the reverse transformation occurred in the formation of cutans compared with a vermiculite-to-HIV transformation in the subtropical soils of central China from north to south. Discussion  The position and environment of cutans in the B horizon together with the pH, organic matter and exchangeable base status in cutans seem conducive to the co-existence of vermiculite and HIV in the soils, but only vermiculite is found in cutans. The transformation of HIV to vermiculite in incubation experiments could be divided into two steps: 1) Cheluviation of organic matter to the interlayer hydroxy-aluminums from HIVs. 2) Rebasification of hydrated cations into the interlayers of vermiculites. Conclusions  The clay minerals in cutans can interact with organic ligands and nutrient elements excreted by roots. Under conditions of frequent wetting and drying and high pH, and when the concentrations of exchangeable bases, iron-manganese oxides, clays, and organic matter are high, the exchangeable cations can be incorporated into the interlayers of HIV, thereby promoting the partial transformation of HIV to vermiculite in rhizosphere soils. Recommendations and Perspectives  Cutan is at the interface of material and energy exchange involved in physical, chemical and biochemical reactions in the rhizosphere. These factors strongly affect the compositions of cutans. HIVs in (upper or adjacent) matrix soils may transform to vermiculites during cutan formation in these special soil environments. ESS-Submission Editor: Jizheng (Jim) He (jzhe@rcees.ac.cn)  相似文献   

6.
ABSTRACT

Radiocesium (RCs) is selectively adsorbed on weathered micaceous minerals (mica) in soils. Although it is clear that weathered mica has selective adsorption sites for RCs, which have been called ‘frayed edge sites (FES),’ the relationship between the degree of mica weathering and the FES content has not been fully investigated. To evaluate the effect of mica weathering on its FES content, we investigated the changes in the FES content with the release of K+ from biotite samples by using sodium tetraphenylborate solution. The FES content was estimated from radiocesium interception potential. The vermiculitic layer charge (Vt charge) was also determined as an indicator of the degree of mica weathering. The amount of K extracted from biotite increased from 154 to 803 mmol kg?1 as the condition of the K extraction was more intensive (i.e., longer time, lower solid/liquid ratio, and higher temperature). As K+ was removed to a greater extent, the FES content increased from 3.96 to 11.5 mmol kg?1, whereas the Vt charge value increased from 17.1 to 329 mmol kg?1. At the earlier stage of mica weathering, the formation of FES was proportional to the increasing amount of K+ released and to the Vt charges. However, at the later stage of mica weathering, when vermiculite was detected by an X-ray diffraction analysis, FES was not necessarily increased in proportion to the increase in K+ released and the amount of Vt charge. These findings indicated that although mica weathering largely increased the FES, the increase was not continuous throughout the weathering stage but evident at the earlier stage of weathering.  相似文献   

7.
《Geoderma》1987,39(3):209-233
Fine-grained, void cutans and grain cappings were observed in the A and upper B horizons of two podzolic soils at a site near Canberra. Optically these features are dark coloured and grainy textured in transmitted, plane-polarized light and generally isotropic in crossed-polarized light. They consist of fine particles ( < 5μm diameter) of quartz, clay minerals, and traces of feldspars and iron and titanium oxides. Electron microprobe analyses indicate high Si:Al ratios, which largely result from the high quartz content of the cutans. Transmission electron microscopy indicated the presence of some poorly structured and only weakly crystalline to possibly amorphous mineral phases consisting of iron, titanium and traces of silicon and aluminium as partial particle coatings and in voids. Mixed-layer clays in the cutans also appeared to have been attacked by weathering on their margins. The presence of euhedral quartz grains suggests that there may have been some authigenic quartz formation within the cutans. Illuvial clays in the lower B and C horizons consist of clear, reddish orange ferri-argillans. It is probable that the reddish orange ferri-argillans developed prior to the grainy cutans, the latter consisting partly of translocated aeolian deposits. Post-depositional weathering of both the grainy cutans and the ferri-argillans has occurred in the A and upper B horizons. Ferrolysis promoted by periodic waterlogging above the textural contrast may be an important weathering process in the A horizons.  相似文献   

8.
Characteristics of Clay Minerals in Podzols and Podzolic Soils   总被引：1，自引：0，他引：1  
The clay minerals in Podzols and podzolic soils developed under coniferous forests in the Subarctic and Cool-temperate zones are characterized by the predominance of smectite and/or mica-smectite interstratified minerals in the eluvial horizons and chlorite-vermiculite intergrade in the illuvial horizons. A large amount of vermiculite is present in the eluvial horizons of some podzolic soils in the Cool-temperate zone. The illuvial horizons of these soils also contain free iron oxides such as goethite. Imogolite and allophane are present in the illuvial horizons of several soils derived from volcanic ashes. It is suggested that the critical bioclimate for the release of interlayered aluminum from the 2:1-type minerals lies between the Cool- and Warm-temperate zone. In the eluvial horizons of Podzols and podzolic soils, mica minerals and chlorite, as primary minerals, have been transformed to smectite through the pedogenic process. Based on previous studies on the structure and degradation of the dioctahedral mica minerals, it is considered that smectite is transformed from 1M-type mica minerals directly, and from 2M-type mica minerals via mica-smectite interstratifled minerals. The formation of a smectite lattice in the eluvial horizon should be a clay-mineralogical indicator of podzolization.  相似文献   

9.
许冀泉  杨德涌 《土壤学报》1964,12(3):275-285
西藏高原突起于我国西南,绝大部分地面的海拔高度在4000米以上,为世界上最高的大高原。它大致在第三纪开始形成,后来曾受第四纪冰川的深刻作用,高山顶部至今仍是冰川的活动场所[1,2]。高原为昆仑山、唐古拉山、喜马拉雅山和横断山等大山脉所盘踞。  相似文献   

10.
Much evidence has indicated that the occurrence of montmorillonite and vermiculite containing Al-interlayers is very common in solis, particularly acid soils. Viewed in the light of soil clay minerology, it would be required to investigate the properties of their original minerals. For the latter purpose, the Al-interlayer has been removed prior to the Mg-glycerol,K-saturation and heating tests for identification of montmorillonite and vermiculite. Its removal has been accomplished in sevsral ways; KOH plus KCl (1), NH4F, KCl plus HCl (2), Na-citrate (3),400C de hydroxylation-NaOH (4) dissolution. Although these methods are effective for the removal of Al-interlayers, they seem drastically to affect the minerals or are time-consuming. Inthe course of the study of hydroxy-Al interlaid complexes of expanding 2:1 layer lattice clay minerals, the authors have noticed the difference between the (001) spacings of hydroxy-Al complexes of montmorillonite and vermiculite; the former exhibited the 20 A basal spacing at room temperature against the 14 A spacing of the latter. This difference might be useful for differentiating montnmorillonite-chlorite intergrades in soils.  相似文献   

11.
Chemical and mineralogical properties of a soil chronosequence in the high mountain zone between 3857 m and 4120 m a.s.l. in Central Nepal (Langtang valley) are presented. The soils have been developed in moraine deposits which consist of acid gneisses. They were classified as Entisols, and Spodosols. XRD analyses of the clay and fine silt fraction show increasing changes with distance from the recent Lirung glacier, depending on the time of deposition, resp. soil age. Alteration of illite to interstratified minerals and to hydroxy-Al interlayered minerals or pedogenic chlorite with increasing soil development could be observed. The interstratified minerals could be identified as random and regular illite-interlayered vermiculite mixed-layer minerals. Intensification of the X-ray signals of the fine silt fraction is given compared to the clay. With increasing soil development differences between the clay and fine silt fraction seem to increase. Indications are given of interstratification of the mica-pedogenic chlorite and chloriteinterlayered vermiculite type in the more intensively weathered soils.  相似文献   

12.
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.

  相似文献   

13.
The biotite changes in the 1–5 μm fraction after its occurrence in the F, H, AE, and E horizons of a pale-podzolic soil for five years under conditions of a model field experiment were assessed by X-ray diffraction analysis. It was found that the main changes of the biotite in all the horizons included the degradational transformation of its crystal lattice to interstratified mica-vermiculite structures and vermiculite. The intensity of this process gradually decreased from the F horizon down the profile in parallel with the decrease in the amount of roots and the abundance and activity of microbiota. Chloritized structures were present among the products of the biotite weathering in the H, AE, and E horizons; the degree of chloritization gradually increased from the H horizon to the E horizon. The main identified products of the biotite weathering in the AE and E horizons formed during the 5 years of the model experiment were identified in the clay and fine-silt fractions from these horizons of the native pale-podzolic soils. Therefore, the vermiculite, soil chlorite, and mixed-layer illite-vermiculite minerals in the soils studied could be considered as products of the recent soil functioning. The obtained results and literature data showed that the weathering of biotite resulted in the formation of K- and Al-buffer systems.  相似文献   

14.
The presence of so-valled chlorite-like minerals has been reported in many soils of not only acid but also of alkaline reaction (1). The minerals have been designated by, many terms, for example, dioctahedral vermiculite (2), dioctahedral analogue of vermiculite (3), 14A mineral (4), chlorite-like mineral (5), interstratified chlorite-vermiculite (6), intergradient chlorite-expansible 2:1 layer silicate, intergradient chlorite-vermiculite, intergradient chlorite-vermiculite-montmorillonite, intergrade, or interlayered vermiculite (7), and 2: 1-2: 2 intergrade (1). The minerals designated by these terms are evidently of the same category, and some of them are synonymous. Although they are of intermediate properties, between true chlorite and true vermiculite or montomorillonite, they could be regarded as an independent group of minerals in the course of pedochemical weathering. Jackson (1), for instance, has given the minerals the position of “weathering index 9”, placing them between vermiculite and kaolin as equivalent to montmorillonite, or secondary chlorite and kaolin in his weathering sequence. An explanation of the diagenesis of the minerals has been recently attempted by synthesis of the chlorite-like structures from montmorillonite (8), (9) and vermiculite (10) and mineralogical analyses of soil clay fractions (7).  相似文献   

15.
Shallow friable red soils (euchrozems) and shallow cracking clays (black earths) occur in close proximity on basalt hills of the Darling Downs of Queensland. The euchrozems are mainly restricted to fiat hill crests and are associated with lithosols; the shallow black earths occur on upper pediment slopes, on small convex crests and on depressions on flat crests. The euchrozems are moderately leached and contain kaolin minerals and hematite with minor montmorillonite, while the black earths are dominantly montmorillonite with minor kaolin and hematite. It is proposed that the euchrozems have developed by long continued weathering under stable well-drained conditions while the black earths have formed in sites prone to erosion and in situations with less water available for weathering. The weathering products produced in each situation have ensured continuation of the processes. The presence of two red soils in anomalous positions have been ascribed to (a) soil formation on exposed ‘bole’ (compacted red clay) layers and (b) local peculiarities of parent material controlling the course of weathering.  相似文献   

16.
The distribution and the availability of Cd, Zn, Cu, and Pb along the entire profile of two highly polluted soils located near Zn smelters have been related to the chemical and mineralogical composition of the soil. Lead and Cu deposits always remain in the surface layers and their availability measured by neutral ammonium acetate extraction was very weak. The behavior of Cd and Zn appears different in sandy acidic podzolic soils and in neutral loamy soils. These metals are associated with the organic matter migration in podzolic soils, while they remain in the upper layers in loamy soils provided that the pH is higher than 6. When the pH drops below 6, the mobility of Cd increases while that of Zn increases only below pH 5. The availability of heavy metals is lower in neutral loamy soils than in sandy acidic soils due to precipitation of carbonates and phosphates. With increasing depth, Cd and Zn are more available if the soil is acid; but, if the soil is neutral and loamy the availability is kept low by adsorption on clays and free oxides. The results of the complex trace metals interactions with the soil components show a higher accumulation capacity for loamy soils than for sandy soils notwithstanding the fact that their CEC is similar.  相似文献   

17.
中国土壤中粘粒矿物的分布规律   总被引：2，自引：0，他引：2  
熊毅  许冀泉 《土壤学报》1964,12(3):266-274
土壤粘粒部分的组成和性质在土壤发生学及土壤肥力特性的研究中都占很重要的位置。过去认为土壤粘粒中的无机物都是非晶形的,自从伦琴射线衍射应用到土壤学研究中后,大家都公认土壤粘粒部分含有晶形结构的矿物。  相似文献   

18.
The composition and the regularities of the profile distribution of the clay minerals in the solods of the Baraba Steppe (ground moistening) and the Priobskoe Plateau (atmospheric moistening) were studied. The two profiles have the distinct eluvial-illuvial distribution of the clay fraction. The composition of the clay fraction in the eluvial layer is dominated by illite. The content of chlorite and labile minerals of the montmorillonite group increases downwards in the profile. The revealed regularities in the profile distribution of the clay fraction and some groups of clay minerals are explained by the joint influence of the mineral dissolution under the influence of the gleying and alkaline hydrolysis, as well as the processes of illitization and lessivage. The major differences in the content and distribution of the clay minerals between the solods and the podzolic soils are the following. The solods have a clear illuvial layer in the clay, while the majority of podzolic soil profiles have the eluvial distribution of the silty fraction. The solods in the eluvial part of the profile and sometimes in even the bottom layers have an unusually high content of the illite minerals in the clay fraction due to illitization. The podzolic layers of the solods do not contain soil chlorites common for the eluvial layers of the podzolic soils, which is due here to a less acidic medium that can not provide the proper conditions of aluminum mobilization and migration needed for the development of chloritization.  相似文献   

19.
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 (rs = 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.  相似文献   

20.
谢萍若 《土壤学报》1987,24(1):18-26
本文研究了温凉湿润地区不同地形条件下花岗岩母质上的山地暗棕色森林土土壤链的矿物风化.结果表明,由阳坡岗顶、中部到阴坡下部,酸性淋溶由强变弱.原生铝硅酸盐矿物蚀变为次生的粘土矿物:黑云母酸-弱酸性→二八面体Al(层间)蛭石弱酸-中性→Al绿泥石;微斜长石→蒙皂石;斜长石弱酸性→高岭石或蒙皂石一高岭石类矿物的混层物.在针阔混交林作用下,A层腐殖酸与铝、铁络合,铝蛭石化过程弱.AB和B层黑云母和长石蚀变强,矿物晶层间羟基铝积累,阳坡岗顶Al(层间)蛭石和蒙皂石化,形成了较高的土壤潜在酸度;阴坡下部除Al蛭石外,并有成土Al绿泥石形成,潜在酸度低.含有蒙皂石的C层,层间铝有积累.矿物蚀变和晶层Al转移,是山地暗棕色森林土酸度的主要来源.红松林类型和林木生长情况与土壤粘土矿物学特性及其化学环境条件密切有关.  相似文献   

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