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1.
For the past ten years much work has been carried out on clay minerals of volcanic ash soils. Most investigators have reported that allophane is dominant among clay minerals of volcanic ash soils and crystallizes to halloysite or meta-halloysite with the advance of weathering (1–8). On the other hand, UCHIYAMA, MASUI and ONIKURA (1960) found that montmorillonite predominates in the clay fraction of volcanic ash soil in Kawatabi (9). Furthermore, MASUI, SHOJI and UCHIYAMA (1966) showed that the major crystalline clay minerals of volcanic ash soils in the Tohoku district are montmorillonite, vermiculite, intergradient montmorillonite-vermiculite and chlorite (10). They also showed that these minerals increase with the advance of weathering and that kaolin minerals are minor constituents. 相似文献
2.
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
3.
Some chemical, physical and mineralogical properties of three soils developed in volcanic ash at altitudes of 1040 m, 1720 m, and 2350 m in Papua New Guinea's Enga Province are presented. Silt-fraction mineralogy and total chemical analyses show that fresh ash occurs in the upper approximately 30 cm of profile at each site. This fresh ash is probably only a few thousand years old and overlies an older weathered ash (Tomba Tephra;more than 50000 years old). At the lowest site the majority of the primary minerals (predominantly amphiboles, volcanic glass and felspar, and some pyroxenes) have been decomposed by weathering to produce a high clay content. With increasing altitude, greater proportions of silt-sized, unweathered and partially altered primary minerals are recognised and molar ratios of calcium, magnesium, sodium and potassium to aluminum increase accordingly. In the clay fractions, allophane with Al/Si ratios of approximately 2.0 is dominant at the highest site, whereas with decreasing altitude lower proportions of allophane occur, Al/Si ratios decline and halloysite becomes dominant. Gibbsite is found in all three profiles 相似文献
4.
Yukiya Horikawa Tetsuro Kitamura Toshimasa Honna 《Soil Science and Plant Nutrition》2013,59(6):779-786
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
5.
Haruo Shindo Daisuke Watanabe Tatsuya Onaga Makiko Urakawa Osamu Nakahara Qiaoyun Huang 《Soil Science and Plant Nutrition》2013,59(5):763-767
Abstrac The effects of 3 oxides (Fe, Al, and Mn oxides) and 3 clay minerals (kaolin, montmorillonite, and allophane) on the adsorption and subsequent kinetic properties of acid phosphatase were compared. The amount of enzyme adsorbed by the oxides and clay minerals followed the order: montmorillonite ? kaolin > Mn oxide > Fe oxide > Al oxide ? allophane. The adsorption isotherms of the enzyme on the oxides and clay minerals, except for montmorillonite and allophane, fitted the Langmuir equation. The activity of the enzyme immobilized by the inorganic components studied was in the order of allophane > kaolin > Fe oxide > montmorillonite > Al oxide ≒ Mn oxide. Compared to the free enzyme, the V max, Km, and V max / K m values of the immobilized enzyme decreased, increased, and decreased, respectively. Among the oxides or clay minerals, the higher the ability of the inorganic components to adsorb the enzyme, the lower the value of the V max / K m ratio of the immobilized enzyme. These findings suggest that the catalytic efficiency of the enzyme complexes formed is determined by the adsorbability of the inorganic components for the enzyme. 相似文献
6.
FLUORIDE ADSORPTION BY ILLINOIS SOILS 总被引：8，自引：0，他引：8
Fourteen surface and 6 subsurface horizons of Illinois soils adsorbed significant amounts of F? with release of OH?. At low concentrations, adsorption was described by both Langmuir and Freundlich isotherms. The calculated Langmuir adsorption capacities were related to pH, clay, organic carbon, and amorphous aluminum contents. Two soils with different gross chemical properties behaved in essentially the same manner, with adsorption maxima occuring between pH 5.5 and 6.5. The similarity between adsorption at different pH values for the soils and those for bauxite, allophane and synthesized ‘soil chlorite’, and the lack of adsorption maxima between pH 5.5 and 6.5 for pure kaolinite and montmorillonite, suggest that F? adsorption in the soils is due primarily to the presence of amorphous aluminum oxyhydroxides which are common weathering products in these soils. 相似文献
7.
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
8.
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
9.
Surface and buried Andosols and buried Luvisols of the Nevado de Toluca Late Quaternary tephra-paleosol sequence (Central Mexico) were studied to show whether these soils present an evolutionary sequence and to determine the pedogenic mechanisms and environmental factors involved in the evolutionary process. Micromorphological observations and mineralogical composition of fine sand and clay fractions were used to detect type and succession of soil-forming process. Some of the buried Andosols, defined as “intergrade” Andosols, have a predominantly blocky structure, humus-depleted areas, redoximorphic features and thin clay coatings in Ah horizons. Clay fractions of buried Andosols contain halloysite besides amorphous components, whereas in modern Andosols, allophane is dominant. Luvisols have micro-areas with granular structure and abundant phytoliths in the groundmass of Bt horizons assumed to be the relict Andosol features. Luvisol clay fractions are dominated by halloysite and kaolinite. Primary minerals show micromorphological weathering features in all studied soils being stronger in Luvisols; however, even in Luvisols, sand fractions consist mostly of unstable volcanic silicates. We hypothesise that the studied profiles form an evolutionary sequence: Andosols–“intergrade” Andosols–Luvisols; the soil transformation is supposed to be linked to progressive crystallisation of 1:1 clay minerals. Comparing the Nevado de Toluca paleosol properties with the existing data on volcanic soil climo- and chronesequences and assessing the regional paleopedological and lacustrine records of Quaternary paleoclimates, we concluded that wet/dry climatic oscillations took place during the formation of the studied paleosols. Rapid crystallisation of 1:1 minerals occurred during dry phases, which speeded up the Andosol to Luvisol transformation and made it independent from the primary mineral weathering status. The Andosol to Luvisol transformation accelerated by climatic fluctuations is thought to be a common soil evolutionary pathway in the subtropical and tropical regions of recent volcanism, which suffered contrasting precipitation oscillations in the Quaternary. 相似文献
10.
Yasuo Kitagawa 《Soil Science and Plant Nutrition》2013,59(2):199-202
The determination of the specific gravity of allophane is an interesting and important problem, but it is no exaggeration to say that we have no satisfactory answer to this question in spite of numerous studies. In this note, the specific gravities of allophane, weathered pumices and volcanic ash soil were determined with a pycnometer, and the values compared with those of the other clay minerals and non-volcanic ash soils. 相似文献
11.
The clay mineralogical composition of soils on volcanic ashes from Mashū and Kamuinupuri-dake volcanoes, Hokkaido, which are rich in cristobalite, was determined using petrological, X-ray diffraction, differential thermal, and selective dissolution and differential infrared spectroscopic methods. The cristobalite occurred in abundance in every size of fraction from coarse sand to clay and every soli from approximately 1,700 to 8,400 years old, and was concluded to be of igneous origin. The major clay minerals were allophanelike constituents and allophane with some layer silicates as the minor clay mineral, being similar to those of andesitic ash soils and different from those of volcanic ash soils containing abundant quartz. The quartz of volcanic ashes was presumed to bederived from the groundmass-equivalent portion of the ashes which had been formed from magma at a low temperature. 相似文献
12.
Tetsuya Eguchi 《Soil Science and Plant Nutrition》2013,59(1):52-64
We examined soils derived from volcanic ash of Kikai-Akahoya tephra on Yakushima Island, Japan, and classified them according to the Unified Soil Classification System of Japan, 2nd Approximation (USCSJ 2nd) and the World Reference Base for Soil Resources (WRB). Five pedons with horizons showing high (>20%) volcanic glass content were investigated. Soils developed under evergreen broad-leaved forests had high acid oxalate-extractable aluminum (Alo) and acid oxalate-extractable silicon (Sio) concentrations, and low acid oxalate-extractable iron (Fe)/dithionite-citrate-extractable Fe ratio. This indicates a warmer climate and less severe leaching conditions compared with soils developed under coniferous forests dominated by Cryptomeria japonica and grasslands dominated by Pseudosasa owatarii. All soils contained considerable amount of hydroxyl-Al-interlayered 2:1 clay minerals. The surface horizons of the pedons developed under the cool-temperate C. japonica forests contained smectite as a result of podzolization. However, the surface horizon of the pedon developed under cool-temperate P. owatarii grasslands did not contain smectite. All pedons belonged to the Kuroboku soils great group (USCSJ 2nd) and Andosols (WRB). Pedons in mountainous areas did not contain horizons with more than 6?g?kg?1 of Sio and hence were classified as non-allophanic Andosols. In mountainous areas, it was observed that allophane formation was inhibited by Al leaching due to intense rainfall (>10,000?mm year?1); Al consumption due to the formation of the Al-humus complex; and Al incorporation into the interlayers of vermiculite. The low soil water pH [pH(H2O)] and leaching of silicon (Si) in mountainous areas would support these anti-allophanic effects. 相似文献
13.
The difficulties in dispersing volcanic ash soils of Japan and New Zealand have been considered to be due to the association or aggregation of allophane (3, 5, 7–10). In particular, MIYAZAWA (9) has obtained evidence that stable microaggregates of Humic Allophane soils derived from volcanic ash have been formed by dehydration of allophane. Recently, several investigators (2, 4, 6, 8, 9, 12) have pointed out that ultrasonic vibration is effective in dispersing the fine particles of soils. With respect to the applicability of supersonic vibration to the particle-size distribution analysis of Humic Allophane soils, MIYAZAWA (9) stated that the maximum dispersion, as measured by the clay content, was obtained only with supersonic vibration using an acidic medium. KOBO and OBA (8) reported that calgon (sodium hexametaphosphate) as a dispersing agent was successfully applicable to most Humic Allophane soils, but the use of HCI was necessary for some highly allophanic subsoils, and that the effect of supersonic vibration on dispersion of the soils is attributed to the breakdown of aggregates larger than 20 microns in diameter. They also recommended a mixture of 10g of soil and 50 ml of water and 20 min. exposure for a supersonic vibrator (10 Kc, 300 W). With respect to the applicability of vibration treatment in the particle-size distribution analysis of Humic Allophane soils containing volcanic glasses in abundance, some apprehension may be entertained about the breakdown of primary minerals, especially of volcanic glasses (9, 10). 相似文献
14.
Allophane has been known to occur widely in volcanic ash soils in Japan and New Zealand. However, exact knowledge of its nature has not been well established, mainly because of extreme difficulty to separate it in pure state and of its x-amorphous nature. In the course of the studies on soil allophane, it was noticed that certain Ando soils contained two different mineral colloids together, in addition to crystalline clay minerals and free sesquioxides. X-ray examination revealed that one was x-amorphous colloid which would be called allophane, and the other an unknown colloid of low crystallinity. Imogolite*** was proposed as the name of the latter colloid by the present authors after imogo in which imogolite was first found. Imogo is a brownish yellow, volcanic ash soil. in the Kuma basin in the Kumamoto Prefecture3). When deferration treatment is applied to the soils, allophane disperses both in an acid and alkaline media, whereas imogolite disperses in an acid medium and flocculates in an alkaline one. 相似文献
15.
《Communications in Soil Science and Plant Analysis》2012,43(9-10):1343-1355
Abstract The cation exchange capacity (CEC) at pH 7 was measured for samples of 347 A horizons and 696 B horizons of New Zealand soils. The mean CEC was 22.1 cmolc/kg for the A horizons and 15.2 cmolc/kg for the B horizons. Multiple regressions were carried out for CEC against organic carbon (C), clay content, and the content of seven groups of clay minerals. The results, significant at p <0.001, were consistent with most of the CEC arising from soil organic matter. For the samples of A horizon, the calculated CEC was 221 cmolc/kg per unit C and for the B horizons was 330 cmolc/kg C. There was also a contribution from sites on clay minerals. Multiple regression indicated that smectite had a higher CEC (70 cmolc/kg) than other minerals but it was not as high as that of type smectites; kaolin minerals had the lowest CEC. There was a significant effect of interaction between organic matter and some clay minerals on the CEC. Samples from B horizons containing allophane had lower CEC than those not containing allophane which is consistent with allophane reacting with carboxyl groups on organic matter. For the samples from the A horizons, however the CEC was higher when allophane was present. 相似文献
16.
H. Gebhardt 《植物养料与土壤学杂志》1976,139(1):73-89
Formation and properties of amorphous clay constituents in soils of the temperate-humid climate region A review of literature and of some own work was given on formation and properties of amorphous clay constituents which occur along with crystalline clay minerals in soils. By that the importance of soil amorphous material with respect to pedologic-agricultural and social-environmental problems was tried to emphasize. At the beginning some clarification of the different terms used for inorganic amorphous clay constituents and a sort of difinition of the different kinds of amorphous materials seemed to be evident. Then, the occurence and the formation of amorphous material in soils of the temperate-humid climate region was commentated. As a result of this it was stated that amorphous clay constituents occur mainly as coatings on negatively charged surfaces of crystalline layer silicates. From the grouping of amorphous substances around negatively charged cores (layer silicates or AlIV-cores in allophanic soils, respectively) it was deduced that the organisation of amorphous clay constituents and allophanes as well as synthetic aluminosilicates might be due to an unique structural principle, which was tried to explain more detailed. The methods used for determination of amorphous materials, especially allophanes, were discussed. Since the determination of amorphous clay constituents by chemical dissolution techniques is ambiguous with respect to soils containing different weathering stages of crystalline layer silicates as well, some suggestions were made for characterizing amorphous substances in soils by cation exchange and anion adsorption properties. Finally the importance of exchange-reactions caused by specific adsorption of ions and molecules (e.g. nutrients and pesticides) was indicated. Furthermore, the possibility was mentioned that harmful environmental substances might be bound (neutralized) and waste nutrients might be recycled by specific adsorption on amorphous soil constituents. 相似文献
17.
Sorptive interactions between Escherichia coli (ATCC 11303B) and a purified allophane clay fraction were studied quantitatively using electronic particle counting and electrophoresis. Adsorption was influenced by pH and ions present at the allophane surface. These effects could be rationalized by considering changes in the net surface charge of the components. Electronic particle counting studies at pH 5.5 and above gave adsorption isotherms that obeyed single-term Langmuir kinetics. At pH 4.5, a more complex two-step isotherm was obtained, which was attributed to aggregation of unadsorbed cells by Al solubilized from the allophane surface. 相似文献
18.
采用批量平衡试验,研究了不同土壤及长黏土矿物对多氯联苯吸附特性。结果表明:多氯联苯浓度范围为0.25~5.0mg L-1时,不同土壤及黏土矿物对多氯联苯的吸附均能用Freundlich方程很好地拟合,随着溶液中多氯联苯浓度的增加,土壤及黏土矿物对多氯联苯的吸附量增加;几种土壤对多氯联苯吸附量大小顺序为:红壤>黄褐土>砂姜黑土,土壤有机质、粘粒等对多氯联苯吸附起主要作用,土壤更易吸附高氯代PCB77;黏土矿物对多氯联苯吸附量大小顺序为:纳米蒙脱石>纳米SiO2>凹凸棒石,黏土矿物吸附多氯联苯能力的大小与黏土矿物的比表面积、粒径、层状结构等有关;多氯联苯本身分子的大小影响其在黏土矿物上的吸附;土壤中添加黏土矿物可以提高对多氯联苯的吸附。 相似文献
19.
Abstract Properties and classification of four selected volcanic ash soils from Abashiri, Hokkaido were studied and the transition of Andisols to Mollisols was discussed. Two of the four pedons (Brown Andosol and Cumulic Andosol)1 showed morphological, clay mineralogical, physical, and chemical properties common to most Andisols in Japan. However, the properties of the other two pedons (Acid Brown Forest soil and Brown Forest soil)1 were considerably different from those of common Andisols in Japan. It was found that the changes in the andic soil properties or transition of Andisols to Mollisols was closely related to the progression of clay weathering, mainly the transformation of noncrystalline clay materials to halloysite. One of the four pedons (Brown Forest soil)1had the clay fraction dominated by halloysite from the uppermost horizon down to the bottom of the profile and satisfied both andic and mollic requirements. Thus we concluded that the pedon is a transitional soil between Andisols and Mollisols and that the transition is closely related to the duration of surface weathering under relatively weak leaching conditions. The four pedons were classified according to the Andisol Proposal (Leamy et al. 1988, New Zealand Soil Bureau) as follows: Pedon 1: Medial, amorphic (allophane/imogolite), frigid Typic Hapludand (Brown Andosol).1 Pedon 2: Medial, amorphic (allophane/imogolite), frigid Typic Melanudand (Cumulic Andosol).1 Pedon 3: Medial, amorphic (allophane/ imogolite), over kandic, frigid Typic Melanudand (Acid Brown Forest soil).1 Pedon 4: Medial, kandic, frigid Typic Hapludand (Brown Forest soil).1 相似文献
20.
The CEC was determined for humic acid preparations by changing the conditions for the CEC procedure and the CEC values obtained were compared with those of clay minerals. Humic acid was extracted from Kodonbaru and Kuriyagawa surface soils, Iwanuma peat, and straw with 0.1 M Na4P2O7-0.l M NaOH. The CEC was measured by a method which eliminates washing for the removal of excess saturating salt. The CEC of humic acid became larger as humification progressed, and increased in the order: Straw<Iwanuma<Kuriyagawa<Kodonbaru. An equilibrium of cation exchange for the humic acid preparations was attained in a short time in contrast with that for allophane. No effect of salt concentration on the CEC of the humic acid preparations was recognized. The CEC of humic acid was also determine using the procedure in which tbe excess salt was removed by washing with water. Practically no decrease of CEC with decreasing salt concentration was found. When the pH of the salt solution WBB reduced, the em: of the humic acid decreased, though the extent of the decrease was smaller than that of allophane. The CEC of halloysite and montmorillonite did not decrease through reduction of the pH of the salt solution. It was considered that humic acid is a stronger acid than allophane and a weaker acid than halloysite and montmorillonite. The difference between the CEC of humic add measured with Ca2+ and Ba2+ was small. Little temperature effect was observed for humic acid. 相似文献