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Is the geological concept of clay minerals appropriate for soil science? A literature-based and philosophical analysis

机译:粘土矿物的地质概念是否适合土壤科学?基于文学的哲学分析

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Data in the literature for soils that are dominated by each of the main types of clay minerals were examined and compared with those for reference clay minerals of the same types to determine the extent to which the nature and properties of clay-size minerals in soils could be explained by those of clay minerals with the same name from non-soil, 'geological' environments. Published information on soils from Australia, New Zealand and Iran was sourced for this study. The clay fractions of each of the soils are dominated by either one of the common phyllosilicates: kaolinite, halloysite, illite/mica, vermiculite, smectite, and palygorskite, or by the nanocrystalline mineral, allophane. Data for samples of kaolinite that had been extracted from soils from several countries (Australia, Thailand, Indonesia and Brazil) and purified before characterization have also been examined. In soils, each dominant clay mineral is generally associated with other materials, including iron oxides, other phyllosilicates and/or nanocrystalline minerals and organic matter. As the most studied example of an extracted phyllosilicate, kaolinite shows a wide range of properties in different soils, but a narrower range of properties within a particular locality. However, almost all of the soil kaolinites studied have larger specific surface areas and higher cation exchange capacities than reference kaolinites. The literature also reveals that, among phyllosilicates in soils, illites have a wide range of potassium contents, expandable minerals (vermiculites and smectites) may be interlayered by hydroxy-Al species particularly, and smectitic layers often occur interstratified with other layers, including those of illite, kaolinite and halloysite. The variability of soil phyllosilicates and their common association with other, often poorly crystallized but highly reactive minerals and compounds can be explained by their formation in the highly heterogeneous and dynamic soil environment. Phyllosilicates from non-soil or geological sources are poor models for the representation of secondary clay-size minerals in soils. In philosophical terms, the reduction of soil mineralogy to mineralogy as it is practiced within geology is misleading because of the differences between the minerals formed in soil and geological environments. In other words, clay minerals as they are defined as mineralogical entities for geology are of a different 'kind' to clay minerals in soils and cannot serve as 'types' or 'stereotypes' to enable explanation of the contribution of secondary clay-size minerals to soil properties or behavior. It is more useful to view clay minerals in soils as secondary inorganic compounds of clay-size than to follow their definition for non-soil purposes as plastic phyllosilicate minerals.
机译:检查了文献中有关每种主要粘土矿物类型的土壤数据,并将其与相同类型参考粘土矿物的数据进行比较,以确定土壤中粘土大小矿物的性质和性质在多大程度上可以用非土壤“地质”环境中同名的粘土矿物来解释。该研究来源于澳大利亚,新西兰和伊朗关于土壤的公开信息。每种土壤的粘土成分均由以下一种常见的层状硅酸盐主导:高岭石,埃洛石,伊利石/云母,ver石,蒙脱石和坡缕石,或纳米晶体矿物铝硅石。还检查了从几个国家(澳大利亚,泰国,印度尼西亚和巴西)的土壤中提取并在表征之前纯化的高岭石样品的数据。在土壤中,每种主要的粘土矿物通常与其他材料结合,包括氧化铁,其他页硅酸盐和/或纳米晶体矿物以及有机物。作为研究最多的提取页硅酸盐的例子,高岭石在不同的土壤中显示出广泛的特性,但在特定区域内显示的特性则较窄。然而,几乎所有研究的土壤高岭土都比参考高岭土具有更大的比表面积和更高的阳离子交换能力。文献还表明,在土壤层状硅酸盐中,伊利石的钾含量范围很广,可膨胀矿物(ver石和蒙皂石)可能被羟基铝物种夹层,并且蒙皂石层经常与其他层(包括硅藻土层)互层。伊利石,高岭石和埃洛石。土壤层状硅酸盐的变异性以及它们与其他通常不易结晶但反应性强的矿物和化合物的共同联系,可以通过它们在高度异质和动态土壤环境中的形成来解释。来自非土壤或地质来源的苯基硅酸盐对于表征土壤中次生粘土大小矿物的模型较差。从哲学上讲,由于在土壤和地质环境中形成的矿物之间的差异,将地质学中的土壤矿物学还原为矿物学是一种误导。换句话说,粘土矿物被定义为地质学的矿物学实体,与土壤中的粘土矿物具有不同的“种类”,并且不能用作“类型”或“定型”来解释次生粘土大小矿物的贡献土壤的性质或行为将土壤中的粘土矿物视为具有粘土大小的次要无机化合物,而不是按照非土壤目的将其定义为可塑性的层状硅酸盐矿物,则更为有用。

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