Adsorption of Cadmium and Zinc onto Micaceous Minerals: Effect of Siderophore Desferrioxamine B

The mobility, bioavailability, and environmental fate of heavy metals in soil are controlled by their adsorption onto soil minerals and solid organic matter. The adsorption is strongly affected by the presence of various low-molecular-weight organic acids. In this study, effect of hydroxamate siderophore desferrioxamine B (DFOB) on cadmium (Cd) and zinc (Zn) adsorption onto two micaceous clay minerals, muscovite and phlogopite, was evaluated in batch experiments. Results showed that the presence of DFOB diminished the adsorption of Cd and Zn onto both minerals, particularly under neutral to alkaline pH conditions. For instance, at pH 8.2, the presence of DFOB caused a decrease in the adsorption of Zn onto phlogopite by nearly 50%. The equilibrium adsorption of Cd and Zn was satisfactorily described using Freundlich isotherm. The adsorption isotherms showed that the affinity of Cd and Zn onto the minerals decreased in the presence of DFOB. For example, at pH 8.0, the presence of siderophore caused a decrease in the Freundlich adsorption isotherm coefficient K_F for Zn adsorption onto muscovite and phlogopite from 4.60 to 0.07 L g^-1 and from 3.56 to 0.36 L g^-1, respectively. These findings confirm the potential influence of siderophore on the fate of Cd and Zn in arid soils containing substantial contributions of micaceous silicate minerals.     

Mineral Composition and Weathering of Soils Derived from Xiashu Loess

Mineralogical, physical and chemical analyses of the soils derived from Xiashu loess were carried out. The primary minerals of these soils were found to be mainly composed of light minerals, such as quartz, feldspar and mica, with traces of heavy minerals. Clay minerals, more complicate in composition, were dominated by hydromica, accompanied by smectite, vermiculite, chlorite, kaolinite, 2:1/1:1 randomly interstratified minerals and small amounts of quartz, goethite, lepidocrocite and hematite, Clay minerals were characterized by low crystallinity and fine particle size. In light of the quartz/feldspars ratio of the 0.01-0.05mm silt fraction, and the clay mineral composition, the freeness of iron oxide, and the silica/sesquioxide and silica/alumina ratios in < 0.002mm clay fraction, it is concluded that the weathering intensity of these soils was lower than those of red soil and yellow earth, but higher than that of brown earth, and that the soil allitization, depotassication and hydroxylation of cl     

Clay mineralogical and ammonium fixation characteristics of some tropical upland rice soils

Abstract

In view of the agronomic and economic significance of NH₄ fixation in soils, an attempt has been made to relate this to the most reactive mineral constituents of soils ‐ the clay minerals, under the temperature‐moisture regimes normal to tropical upland rice soils. Laboratory fixation study was done with NH₄, concentrations similar to those common in soils upon N fertilization, and under alternate wetting and drying at ambient temperatures rather than at 100°C as in many published studies.

Results of the investigation show that soil clays with dominant vermiculite and montmorillonite fix the greatest proportion of applied NH₄ (94 and 91%), followed by beidellite (72%) and x‐ray amorphous (45–64%) clays. Fixation is negligible (10%) in the clay with mineral suite consisting of hydrous mica, halloysite, and chlorite. Crystallinity of minerals seems to influence NH₄ fixation appreciably.     

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.     

富钾植物籽粒苋(Amaranthus spp.)对土壤矿物钾的吸收利用研究

运用土培、石英砂培、有机酸释钾实验及矿物X衍射分析研究了不同基因型籽粒苋(Amaranthusspp.)对土壤矿物钾的吸收利用及其机制。结果表明,籽粒苋能有效地利用土壤和云母(黑云母和金云母)中的钾;籽粒苋品种R104、CX4对钾的吸收量高于一般型品种(CX77);籽粒苋根系能引起云母矿物向蛭石转化;籽粒苋根系分泌物中的草酸比一般有机酸具有更高的释放矿物中钾素的能力。     

Source minerals and formation of partially interlayered vermiculites in Dystrochrepts derived from Tertiary sediments

The formation of partially interlayered vermiculite (PIV) was studied in six Dystrochrepts derived from Tertiary sediments. Mineralogy of silt and clay fractions of gravel and fine earth separated from surface and subsurface samples were determined by X-ray diffraction. PIV, mica, vermiculite and regularly interstratified 1:1 PIV/chlorite (PIV/Ch(l:l)) were the dominant clay minerals. The contents of these minerals were compared between the specific particle-size fractions of gravel and fine earth for each sample and the difference was interpreted in terms of mineral transformation associated with soil formation. PIV was formed from mica and PIV/Ch(l:l) in soils with a pH(KCl) of 3.5 to 4.0 and little organic matter. Vermiculite was formed from mica in surface soils with a low pH (pH(KCl) 3.5) and abundant organic matter. PIV would form directly from mica without an intermediary phase of vermiculite and form from PIV/Ch(l:l) by partial dissolution of interlayers in chlorite layers.     

Specific Features of Profile Distribution and Crystallochemistry of Phyllosilicates in Soils of the Cisbaikal Forest-Steppe

The mineralogical composition of agrogray, dark gray, and agro-dark gray soils (Luvic Greyzemic Retic Phaeozems); agro-dark gray residual-calcareous soils (Calcaric Cambic Phaeozems); clay-illuvial agrochernozems (Luvic Chernic Phaeozems); and agrochernozems with migrational–mycelial carbonates (Haplic Chernozems) developed in the forest-steppe of Central Siberia within the Irkutsk Depression has been studied. The clay (<1 μm) fraction separated from these soils consists of mixed-layer minerals with alternating layers of hydromica, smectite, vermiculite, and chlorite; the proportions between them change within the soil profiles. The clay fraction also contains hydromicas, kaolinite, chlorite, and some admixture of the fine-dispersed quartz. Each type of the soils is characterized by its own distribution pattern of clay material with specific alternation of layers in the mixed-layer formations. Mixed-layer minerals of the chlorite–vermiculite type predominate in the upper horizons of texture-differentiated soils. Down the soil profile, the content of mixed-layer mica–smectitic minerals increases. In the clay fraction of arable dark gray-humus soils with residual carbonates, the distribution of the clay fraction and major mineral phases in the soil profile is relatively even. An increased content of well-crystallized kaolinite is typical of these soils. The parent material of agrochernozems has a layered character: the upper horizons are generally depleted of clay, and the middle-profile and lower horizons are characterized by the considerable kaolinite content. In general, the clay material of soils of the Tulun–Irkutsk forest-steppe differs considerably from the clay material of foreststeppe soils developed from loesslike and mantle loams in the European part of Russia. In particular, this difference is seen in the proportions between major mineral phases and between biotitic and muscovitic components, as well as in the degree of crystallinity and behavior of kaolinite 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.     

含钾矿物中钾的释放及其与溶液环境中离子种类的关系

通过室内试验研究探讨5种含K矿物中K在不同溶液中的释放规律(释放量和释放速率).结果表明,不同含K矿物中K释放速率和释放量的顺序均表现为:黑云母>蛭石>金云母≥白云母>钾长石,不同K矿物释K速率在酸溶液中差异最大,其次在钙和钠盐溶液中,在水中的速率差异最小,这主要是受其矿物本身结构的影响.不同离子对含K矿物中非交换态K释放的促进作用差异显著:H~+>>Ca~(3+)>Na~+>H_2O>NH_4~+.随矿物K有效性增加,H~+和Ca~(2+)对矿物K释放的促进作用越大,而且H~+较Ca~(2+)对黑云母、金云母和长石中的K有更突出的促释作用.此外,Ca~(2+)较Na~+显著促进了黑云母和蛭石中K的释放,但对其他矿物中K释放的影响两者无显著差异.NH~+_4则显著抑制了各种矿物中K的释放,对黑云母和蛭石的抑制作用更强于对金云母和白云母的作用.     

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.     

The dissolution of micas by fulvic acid

Three micas commonly occurring in soils, that is, biotite, phlogopite and muscovite, were shaken with 0.2% (W/V) aqueous fulvic acid (FA) solution for 710 h at room temperature. Proportions of major constituent elements extracted (Fe, Al, Mg, K and Si from biotite, Al, Mg, K and Si from phlogopite and Al, K and Si from muscovite) were determined.Depending on the type of mineral and its Fe content, substantial amounts of Fe, Al, Mg, K and Si were brought into aqueous solution by the FA under mild conditions. The ease with which the micas were attacked by the FA decreased in the following order: biotite > phlogopite > muscovite. IR and ESR analyses indicated the formation of metal—FA complexes as a major reaction mechanism by which the minerals were dissolved. Our data show that aqueous FA solution can dissolve from micas relatively large amounts of metals and Si, which may then become more available to plant roots and microbes, active in soil genesis processes, as well as participants in the synthesis of new minerals.     

四苯硼钠溶液中含钾矿物非交换态钾的释放特性研究

含钾矿物的全钾含量、非交换态钾总量以及非交换态钾的释放速率因矿物种类而异,且3种参数之间没有必然的相关性。供试5种含钾矿物非交换态钾总量由高到低的顺序是:金云母 5.19% 黑云母3.08% 蛭石2.01% 白云母1.18% 钾长石0.24%,占各矿物全钾的比例分别为:58.4% 、99.7% 、62.5% 、14.2% 和4.98% ,平均达48%。选择较弱提取力的四苯硼钠溶液进行非交换态钾的释放特性研究,5种矿物非交换态钾3d释放累积量顺序为:黑云母 蛭石 金云母 白云母 钾长石;非交换态钾平均释放速率也表现为同样的顺序。上述5种矿物在弱提取力的四苯硼钠溶液中释放3 d,非交换态钾的平均释放速率分别为5.99、2.34、0.52、0.22和0.17 mg/(kgmin),差异明显。如何根据非交换态钾的释放量和释放速率来综合评价矿物钾的生物有效性是未来研究中需要明确的问题。     

Soil clay mineralogies in relation to fertility management: Effect of soil clay mineral compositions on potassium fixation under conditions of wetland rice culture

Abstract

To evaluate the impact of soil clay mineralogy on the utilization efficiency of potassium fertilizers by rice, potassium fixation studies were made on fourteen soil clays having a range of mineralogical compositions. Soil clay with monomineralic beidellite fixed the highest proportion (76%) of the added potash, followed by clays containing either dominant or major vermiculite (51–66%). Fixation was significantly less severe (<35%) in vermiculitic clays containing hydrous mica. All the clays with mineralogical suites without beidellite or vermiculite, but consisting of montmorillonite, chlorite, hydrous mica, halloysite, kaolinite, and x‐ray amorphous material did not fix appreciable amounts (<18%) of the applied potassium.     

Potassium release on drying of soil samples from a variety of weathering regimes and c clay mineralogy in China

Thirty two soil samples from China were analyzed for exchangeable K before and after drying. Most soil samples were higher in exchangeable K after air-drying and ovendrying (60°C) than when wet. Soil clay minerals, especially clay-size mica, affected K released in air-dry and oven-dry samples. According to composition of clay minerals of air-dried samples, five classes were recognized. Soil samples with high mica and montmorillonite have the highest exchangeable K. Samples that contained higher kaolinite than mica had lower exchangeable K. Samples with higher kaolinite than quartz and mica had still lower exchangeable K. Samples of sandy soils contained very low exchangeable K. When quartz was the main mineral, the samples that had kaolinite and gibbsite as the main clay minerals had very low exchangeable K. The degree of weathering (weathering mean) bore an inverse relationship to the amount of K released on drying in air or at 60°C. Udults and Udalfs (Red Earths) of southeastern China, because of their high K release on being dried, are inferred to have received fine mica from the Western Desert dust rainout, reported to Liu et al. (1981).     

Characteristics of Clay Minerals in Podzols and Podzolic Soils

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.     

Distribution and development of sclerotium grains as influenced by aluminum status in volcanic ash soils

Granulometric and clay mineralogical analyses were performed on soil types differing in their genesis which had been formed on the raised coral limestone terraces and plateaux under the perhumid subtropical maritime climate of the Ryukyu Islands. The amount of clay fraction in Rendzina-like soil on the lower terrace was relatively small (8-34%) and decreased with depth, while those in Terra fusca-like soils on the middle terraces and in Terra rossa-like soil on the plateau were very large (45–78%) suggesting the occurrence of clay migration.

Rendzina-like soil mainly contained illite and metahalloysite with a moderate amount of mixed layered mineral consisting of illite and vermiculite, and a small amount of vermiculite, Al-vermiculite, goethite, and quartz. Clay mineral composition of Terra fusca-like and Mottled Terra fusca-like soils was similar to that of Rendzina-like soil except that the content of illite was lower in these soils. Terra rossa-like soil, on the other hand, mainly contained Al-vermiculite, metahalloysite, and gibbsite, indicating a highly advanced stage of hydroxyaluminium interlayering. Differences in clay mineral composition from that of Rendzina, Terra fusca, and Terra rossa soils in the European countries were recognized, in that mont-morillonite was absent and hydroxyaluminium interlayering actively proceeded in the soils studied here. This finding is considered to reflect the rapid alteration and intense hydroxyaluminium interlayering of clay minerals under the perhumid subtropical conditions.     

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

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

中国土壤中粘粒矿物的分布规律

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。     

SANDSTONE-DERIVED SOILS OF A CATENA AT IPERU, NIGERIA

Chemical and mineralogical properties of five soil profiles of a catena in Iperu, Western State of Nigeria, are reported. The pH values of the subsoils are extremely acid. Acidity decreases with improved drainage in the subsoils (pH 4.0–5.8). The cation exchange capacity (C.E.C.) of the soils range from 3.0 to 16.2 me/100g of soil. The silt: silt+clay ratio, calcium: magnesium ratio and Fe₂O₃:Al₂O₃ ratio are used as weathering indices. The low values of the silt: silt + clay index indicate that the soils must have undergone advanced weathering. The magnitude of the Ca: Mg ratio indicates that more calcium than magnesium is available in the soils. The values for sodium and potassium are extremely low. More iron than aluminium was extracted from the soils by the dithionite-citrate method. Kaolinite is the most abundant clay mineral. Halloysite, interstratified clay materials, vermiculite, quartz, and mica are present in considerable amounts. The silt fraction in which quartz is the most abundant mineral, also contain some kaolinite and mica.     

中国土壤胶体研究 Ⅵ.西藏高原几种主要土壤的粘土矿物组成和演变

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。