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Suitability of the ESS laboratory method to determine the equilibrium soil solution composition of agricultural soils, and suggestions for simplification of the experimental procedure

机译:ESS实验室方法确定农业土壤平衡土壤溶液组成的适用性,以及简化实验程序的建议

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The proper selection of the background electrolyte is of special importance studying element availability and mobility in the laboratory. The determination of the background solution composition can be done with the equilibrium soil solution method ESS (Matschonat and Vogt, 1997). The ESS method is a procedure to find out a salt solution of major cations and anions that does not undergo changes in its composition when brought into contact with a specific soil sample. This composition is experimentally approximated in an iterative procedure until certain quality criteria are fulfilled. We tested if the ESS method, which was developed for forest soils, can successfully be applied also to agricultural soils. The solution composition was confirmed by an independent method. We used samples of a glasshouse and an arable loess soil. Because the ESS method is relatively time and work consuming, we tested modifications which should simplify the procedure: the use of dried and frozen samples instead of field fresh soil, an approximation according to the solution's electric conductivity only, and the modeling of cation exchange to omit iteration steps. The ESS method caused slight overestimation (10-25 %) in cation concentrations, but in general, these were well met. Individual anion concentrations, however, were not buffered in this soil and could not unequivocally be determined. We recommend to adjust the anion concentrations in the ESS procedure according to their proportions in an initial water extract. As ion concentrations are functions of the soil : solution ratio, any method based on addition of water to the soil, like the so-called soil saturation extract (Germany: Bodensattigungsextrakt), runs a risk to seriously underestimate ion concentrations at field conditions. The ESS method may therefore be especially well suited for soils with a low water content. The use of frozen soil gave good results and the omission of iteration steps by cation exchange modeling was promising and will be explored with the aim to operationalize it in forthcoming work.
机译:正确选择背景电解质对研究实验室中元素的可用性和迁移率特别重要。可以使用平衡土壤溶液法ESS(Matschonat and Vogt,1997)确定背景溶液的组成。 ESS方法是一种查找主要阳离子和阴离子的盐溶液的步骤,当与特定的土壤样品接触时,该盐溶液的成分不会发生变化。在迭代过程中以实验方式近似此组成,直到满足某些质量标准为止。我们测试了针对森林土壤开发的ESS方法是否也可以成功地应用于农业土壤。通过独立方法确认溶液组成。我们使用了温室和可耕的黄土土壤的样本。由于ESS方法相对耗时且费力,因此我们测试了可简化程序的修改方法:使用干燥和冷冻的样品代替田间新鲜土壤,仅根据溶液的电导率进行近似计算,以及将阳离子交换建模为省略迭代步骤。 ESS方法导致阳离子浓度略有高估(10-25%),但总体而言,这些都可以很好地满足。但是,各个阴离子的浓度并未在该土壤中缓冲,因此无法明确确定。我们建议在ESS程序中根据初始水提取物中阴离子的比例调整阴离子浓度。由于离子浓度是土壤:溶液比率的函数,因此任何基于向土壤中添加水的方法(例如所谓的土壤饱和提取物(德国:Bodensattigungsextrakt))都可能会严重低估田间条件下的离子浓度。因此,ESS方法可能特别适合于含水量低的土壤。冻土的使用取得了良好的结果,阳离子交换模型的省略迭代步骤是有希望的,并将在今后的工作中进行探索。

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