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1.
Data on the composition and properties of soil adsorption complex in the virgin and ameliorated meadow-chestnut soils in the northern Caspian region are generalized. It is shown that the experimental values of the effective CEC in the A1 horizon are lower than those calculated on the basis of data on the organic matter content and the content and mineral composition of fine fractions. We explain this discrepancy by the interactions between the organic matter and clay minerals resulting in the blocking of a part of the exchangeable positions. In the BC horizon, the experimental values of the effective CEC are twice as high as those calculated from the data on the amount of labile clay minerals in fine fractions. This can be explained by the presence of sorption centers on poorly crystallized illites and chlorites in the clay fraction and by the partial aggregation of clay material into coarser fractions that cannot be destroyed upon the separation of clay fractions by the Aidinyan procedure, which leads to the underestimation of the clay content.  相似文献   

2.
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   

3.
Profiles of arid and semi‐arid zones soils of Punjab, northwestern India, were investigated for different forms of iron (Fe): total Fe, diethylenetriamine penta‐acetic acid (DTPA)–extractable Fe, soil solution plus exchangeable Fe, Fe adsorbed onto inorganic sites and oxide surfaces, and Fe bound by organic sites. Irrespective of the different fractions of Fe present, its content was higher in the fine‐textured Alfisols and Inceptisols than in the coarse‐textured Entisols and Aridisols. Lower content of total Fe was observed in the surface horizon and then increased in the subsurface horizons, whereas no set pattern was observed in Entisols. Also, irrespective of the soil orders, the contents of different forms of Fe were higher in the surface horizon and then decreased by depth. None of the forms of Fe exhibited any consistent pattern of distribution.

Organic matter and the content of clay and silt fractions had a strong bearing on the distribution of forms of Fe. Based on a linear coefficient of correlation, the soil solution plus exchangeable Fe adsorbed onto inorganic sites and DTPA‐extractable Fe increased with increase in soil organic carbon but decreased with increase in soil pH and calcium carbonate content. Total Fe increased with increase in cation exchange capacity (CEC) and clay and silt content. The results also revealed that there was equilibrium in different fractions of this element. Among the different Fe forms, Fe bound by organic sites, water‐soluble plus exchangeable Fe, and Fe adsorbed onto oxides (amorphous surfaces) were positively correlated with the DTPA‐extractable Fe. Though some forms are interrelated, none of the forms had any relationship with the total Fe.  相似文献   

4.
The organic matter in soils may be stabilized by its interactions with minerals. We have studied such interactions in a Haplic Alisol under forest in which clay and organic matter have migrated from an eluvial A horizon to accumulate in an illuvial B horizon. We have tried to trace the fate of organic matter in these horizons (Ah and Bvt) by determining clay mineralogy, carbon and nitrogen content, hydrolysable amino acids, lignin signature by alkaline CuO oxidation and carbon species by 13C CPMAS NMR of bulk soils and particle‐size fractions. In both horizons, most of the organic matter was present in O–alkyl and methylene structures, each contributing one‐third to the bulk organic matter. In the Ah horizon the ratios of carbon‐to‐nitrogen, and yields for lignin and hydrolysable amino acids decreased as the particle‐size class decreased, but side‐chain oxidation of lignin compounds increased with decreasing particle size. In contrast to previous observations, the proportions of O–alkyl carbon increased as particle size decreased, constituting a major proportion of the organic carbon in the clay‐size fractions from both the Ah and Bvt horizons (≥ 38%), while proportions of methylene carbon decreased. Illite was the dominant mineral in the fraction ≤ 6 μm, whereas the mobile fine clay fraction (<0.2 μm) was rich in smectites – minerals with large surface areas. Our results support the hypothesis that potentially labile organic matter, such as O–alkyl carbon typically present in polysaccharides, may be stabilized against further degradation in organomineral complexes.  相似文献   

5.
The cation exchange capacity (CEC) and specific surface properties were investigated in four particle‐size fractions < 50 μm from three loess (one Kastanozem and two Phaeozems), a holocene (Fluvisol) and a basalt soil (Nitisol) before and after destruction of organic matter. Particle‐size fractions were separated by sedimentation after chemical and physical dispersion of the soil samples. Illite, amorphous minerals, mixed layers, smectite and kaolinite were the predominant clay minerals. They were detected in all size fractions. The CEC increased with increasing organic matter contents and this effect was more pronounced in coarser fractions. The organic matter content per unit surface area was two or three times larger in coarse silt than in clay, irrespective of the soil type.  相似文献   

6.
胡敏酸对铵钾在粘土矿物上交互作用的影响   总被引：1，自引：0，他引：1  
Interaction of ammonium (NH+4) and potassium (K+) is typical in field soils. However, the effects of organic matter on interaction of NH+4 and K+have not been thoroughly investigated. In this study, we examined the changes in major physicochemical properties of three clay minerals (kaolinite, illite, and montmorillonite) after humic acid (HA) coating and evaluated the influences of these changes on the interaction of NH+4 and K+on clay minerals using batch experiments. After HA coating, the cation exchange capacity (CEC) and specific surface area (SSA) of montmorillonite decreased significantly, while little decrease in CEC and SSA occurred in illite and only a slight increase in CEC was found in kaolinite. Humic acid coating significantly increased cation adsorption and preference for NH+4, and this effect was more obvious on clay minerals with a lower CEC. Results of Fourier transform infrared spectrometry analysis showed that HA coating promoted the formation of H-bonds between the adsorbed NH+4 and the organo-mineral complexes. HA coating increased cation fixation capacity on montmorillonite and kaolinite, but the opposite occurred on illite. In addition, HA coating increased the competitiveness of NH+4 on fixation sites. These results showed that HA coating affected both the nature of clay mineral surfaces and the reactions of NH+4 and K+with clay minerals, which might influence the availability of nutrient cations to plants in field soils amended with organic matter.  相似文献   

7.
Soil organic matter in Mollisols is often preserved for an extremely long period (e.g. > 3000 years). We confirmed that the stable organic matter in Mollisols is the medium to coarse sized (0.2–2.0 μm) clay-humus complex with humic acid combined with calcium as the main organic constituent. The argillic horizon contained relatively large amounts of clay-humus complexes and had relatively high carbon contents, humic acid/fulvic acid ratios and degrees of humification of humic acid. Medium clay and coarse clay fractions preserved the organic carbon most efficiently. Highly humified humic acid could be detected even in the uppermost part of the Ah horizon and was probably stabilized in lower horizons by forming a complex with clay fractions.  相似文献   

8.
Abstract

Recently agricultural activity in the mountainous area of northern Thailand has increased and problems relating to soil fertility have arisen. In order to gain basic information about the soil properties associated with shifting cultivation, physicochemical properties of the surface soils (0–10 cm) and subsoils (30–40 cm) were investigated in selected villages in the area. The physicochemical properties of the soils studied are summarized as follows: 1) The soils were rich in organic matter, content of which ranged from 11.4 to 63.3 g C kg?1 in the surface soil. 2) The pH(H2O) of the soils mostly ranged from 5 to 7 and soil acidity was more pronounced in the deeper horizons. In the surface soils, exchangeable Ca and Mg were generally dominant, whereas exchangeable Al was often predominant in the subsoils. 3) Most of the soils showed a medium to fine texture with more than 30% clay. The clay mineral composition was characterized by various degrees of mixture of kaolin minerals and clay mica with, in some cases, a certain amount of 2:1-2:1:1 intergrades. 4) According to the ion adsorption curves, most of the B horizon soils were characterized by the predominance of permanent negative charges. On the other hand, organic matter contributed to the increase of variable negative charges in the surface soils. The content of organic matter and the percentage of the clay fraction were essential for determining the CEC of the soils of the surface 10 and 30–40 cm depths, respectively. Under the field conditions, the composition of exchangeable cations largely reflected the soil acidity. In addition, the content of organic matter also showed a significant correlation with that of available N in the surface soils. Thus, soil acidity both in the surface soils and subsoils, organic matter content in the surface soils, and clay content in the subsoils were considered to be the main factors that affected soil chemical fertility in the area.  相似文献   

9.
Abstract

Many of the cultivated soils of sub‐Saharan Africa typically have a surface horizon low in clay and with a low cation exchange capacity (CEC). In these soils, CEC is largely due to the soil organic matter (SOM). Measurements made on long‐term trials show that changes in CEC and SOM are positively correlated to one another, but not of same magnitude, suggesting that not all of the SOM plays an equal role as regards the soil CEC. To study the influence of the different SOM size fractions on the CEC, soils with or without application of manure or compost coming from trials in Chad and Côte d'Ivoire were separated without destruction of the SOM into five organo‐mineral fractions: “coarse sand”;, “fine sand”;, “coarse silt”;, “fine silt”;, and “clay”; made up of particles of sizes between 2,000 and 200, 200 and 50, 50 and 20, 20 and 2, and 2 and 0 μm, respectively. Fractionation was carried out by mechanical dispersion of the soil, wet sieving of the fractions larger than 20 μm, and decanting of the “clay”; and “fine silt”; fractions. The CEC of these fractions increases inversely with their size. The “clay”; fraction which contains half of the SOM contributes about 80% of the CEC of the soils. The CEC of the fractions is largely a function of their carbon (C) content, but the organic CEC per unit C of the “clay”; fraction appears to be four times greater than that of the other fractions (1,000 as against 270 cmolc kg‐1). Applications of manure or compost increase the CEC of the soils by increasing the soil C only when this C increase concerns the fine fractions of the SOM.  相似文献   

10.
Abstract

Profiles of semi‐arid–zone soils in Punjab, northwest India, were investigated for different forms of zinc (Zn), including total, diethylenetriamine penta‐acetic acid (DTPA)-extractable, soil solution plus exchangeable (Zn), Zn adsorbed onto inorganic sites, Zn bound by organic sites, and Zn adsorbed onto oxide surfaces. Irrespective of the different fractions of Zn present, its content was higher in fine‐textured Alfisols and Inceptisols than in coarse‐textured Entisols. In general, the higher content of Zn was observed in the surface horizon and then decreased in the subsurface horizons. However, none of the forms of Zn exhibited any consistent pattern of distribution. Organic matter and size fractions (clay and silt) had a strong influence on the distribution of different forms of Zn. Based upon the linear coefficient of correlation, the soil solution plus exchangeable Zn, adsorbed onto inorganic sites, and DTPA‐Zn increased with increase in organic carbon but decreased with increase in pH and calcium carbonate content. Total Zn increased with increase in clay and silt content. Among the different forms, Zn bound by organic sites, water soluble plus exchangeable Zn and Zn adsorb onto oxide (amorphous surfaces) were all correlated with DTPA extractable Zn. The uptake of Zn was more in recent floodplain Entisols than very fine textured Alfisols and Inceptisols. Among the different forms soil solution +exchangeable and DTPA‐extractable Zn was positively correlated with total uptake of Zn.  相似文献   

11.
Agricultural, environmental and ecological modeling requires soil cation exchange capacity (CEC) that is difficult to measure. Pedotransfer functions (PTFs) are thus routinely applied to predict CEC from easily measured physicochemical properties (e.g., texture, soil organic matter, pH). This study developed the support vector machines (SVM)‐based PTFs to predict soil CEC based on 208 soil samples collected from A and B horizons in Qingdao City, Shandong Province, China. The database was randomly split into calibration and validation datasets in proportions of 3:1 using the bootstrap method. The optimal SVM parameters were searched by applying the genetic algorithm (GA). The performance of SVM models was compared to those of multiple stepwise regression (MSR) and artificial neural network (ANN) models. Results show that the accuracy of CEC predicted by SVM improves considerably over those predicted by MSR and ANN. The performance of SVM for B horizon (R2 = 0.85) is slightly better than that for A horizon (R2 = 0.81). The SVM is a powerful approach in the simulation of nonlinear relationship between CEC and physicochemical properties of widely distributed samples from different soil horizons. Sensitivity analysis was also conducted to explore the influence of each input parameter on the CEC predictions by SVM. The clay content is the most sensitive parameter, followed by soil organic matter and pH, while sand content has the weakest influence. This suggests that clay is the most important predictor for predicting CEC of both soil horizons.  相似文献   

12.
水稻子实对不同形态重金属的累积差异及其影响因素分析   总被引：3，自引：0，他引：3  
在分析成都平原核心区土壤重金属(Cd、Cr、Pb、Cu、Zn)全量、各形态含量及相应点位种植的水稻子实重金属含量的基础上,通过统计分析、空间插值及线性回归方程的模拟,研究了土壤Cd、Cr、Pb、Cu、Zn全量的空间分布状况、各形态重金属含量统计特征,以及水稻子实对重金属各形态的累积差异及其影响因素。结果表明,成都平原水稻土重金属污染较轻,除Cd外,均低于国家土壤环境质量二级标准。土壤中重金属的可交换态含量均较低,Cd主要以铁锰氧化态存在,Cr、Cu、Zn、Pb主要以残渣态存在。水稻子实对5种重金属的累积效应顺序为:Cd>Zn>Cu>Pb>Cr。与水稻重金属累积关系密切的重金属活性形态(可交换态、碳酸盐结合态、铁锰氧化物结合态和有机物结合态)主要有:Cd的碳酸盐结合态、Cr的可交换态、Pb的有机物结合态和Cu的碳酸盐结合态含量;Zn各活性形态对水稻子实含量的影响不明显。土壤理化性质对不同活性形态重金属元素的影响效应各不相同。活性态Cd主要受有机质、pH和容重的影响;活性态Cr与pH、有机质、CEC和容重密切相关;活性态Pb与有机质、容重、中细粉粒、砂粒等均有密切的关系;Cu的活性主要受粘粒、有机质含量的影响;Zn的有效性主要受pH、有机质、砂粒、容重的影响。总的看来,对土壤Cd、Cr、Pb、Cu、Zn各活性形态含量影响效应较强的是有机质、pH、容重,而与土壤吸附性能密切相关的颗粒组成、CEC的影响不甚明显。  相似文献   

13.
Abstract

In soil samples from two study sites in southern Norway, exchangeable cations were determined using two different ammonium (NH4)‐salts as extractant. As expected, the cation exchange capacity (CEC) determined in 1M ammonium acetate (NH4OAc), buffered at pH 7.0 was higher than the CEC measured in ammonium nitrate (NH4NO3). By contrast, the amount of exchangeable calcium (Ca), magnesium (Mg), and barium (Ba) was lowest in the NH4OAc extract, in particular in the upper soil horizons high in organic matter (O‐ and E‐horizon). This suggests that NH4 in 1M NH4OAc does not compete effectively with multivalent base cations. The relatively high levels of exchangeable base cations in NH4NO3 could not be explained by increased weathering. An increase in selectivity of especially divalent cations may explain the relatively low amount of exchangeable base cations extracted by NH4OAc, as this involves increased deprotonation and thus a higher negative charge.  相似文献   

14.
We used the specific surface area (SSA), the cation exchange capacity (CEC) and the content of dithionite‐extractable iron (Fed) to predict the content of organic carbon in illitic clay fractions of topsoils from loess. We determined SSA (BET‐N2 method) and CEC of clay fractions after removing organic C or reducing oxides or both. The CEC and the SSA of the carbon‐ and oxide‐free clay fraction explained 56% and 54% of the variation in C content, respectively. The Fed content of the clay fractions was strongly and negatively related to the C content, and with the SSA of the carbon‐free clay fraction it predicted C content almost completely (R2 = 0.96). The results indicate that the amount of cations adhering to the silicate clay minerals and the size of the silicate mineral surface area are important properties of the mineral phase for the storage potential of C. The reason for the negative relation between iron oxides and C content remains unclear.  相似文献   

15.
The natural Sr isotope composition of acid leached soils developed on loess, under beech forest, in central Belgium was used as a tracer of soil forming processes, in conjunction with physico‐chemical and quantitative mineralogical investigations. Attention was focused on weathering and exchange processes, with special emphasis on the origin of the current soil exchangeable fraction and the influence of the atmospheric deposition and biological cycling on the calcium exchangeable pool (Sr acts as a proxy for Ca). The determination of 87Sr/86Sr ratios was made on the bulk soil, on the clay‐ and silt‐size soil separates, on 0.1 m HCl extracts, on the labile pool, on the soil solution and on the bulk precipitation. The acid leached soil profiles are characterized by a sequence of weathering processes that is highlighted by both mineralogical and isotopic changes. From the calcareous unweathered loess (pH 7.5) to the uppermost soil horizons (pH < 4.0) the evolution of the 87Sr/86Sr isotope ratio clearly reflects: (i) the selective weathering of Ca‐plagioclase (small 87Sr/86Sr ratio) and the increasing proportion of resistant K‐ and Rb‐rich minerals (large 87Sr/86Sr ratio) in the uppermost soil horizons; and (ii) a downward translocation of clay minerals with a large isotopic ratio, a physical breakdown of muscovite and a non‐congruent chemical weathering of K‐feldspar. The influence of organic restitutions or atmospheric deposition is not significant. The comparison between the Sr isotopic signature of the soil solution, and the exchangeable and HCl‐extractible soil fractions provides information about cation exchange efficiency, soil–water interaction and the origin of the exchangeable pool.  相似文献   

16.
A soil's cation exchange capacity (CEC) is expected to be relatively inert against changes in cation loading. In this study, we treated a soil sample originating from the organic layer of a forest soil with various bivalent cations after removing the native cations. Sorption isotherms and cation exchange capacity were determined, the latter using the BaCl2 method. Sorption showed Langmuir characteristics, with the maximum coverage (Qmax) increasing in the order Ba2+ < Ca2+ < Mg2+, but being clearly smaller than the initial load of native exchangeable cations. The Langmuir coefficient, kMe, depended oppositely to the order obtained for Qmax. CEC increased upon cation treatment and it varied by a factor of almost two. The unexpected variation of CEC was explained by the low cation exchange capacity of the organic matter such that not all functional groups are close enough to be bridged and the second charge of a bivalent cation is not neutralized by the organic functional group. The Langmuir sorption type, and Qmax being smaller than the content of sorption sites and being largest for Mg, suggested that only a part of the sites can be cross‐linked and at least part of the cross‐links are formed by hydrated cations. Thermodynamic considerations allowed reconstruction of two contrasting processes during CEC determination by Ba2+: Case A: the disruption of cross‐links, which increases with the cationic strength and the cation load before CEC determination, but does not require structural re‐orientation in the SOM matrix, and Case B: the formation of new cross‐links during CEC determination, depending only on the content of unoccupied sites before CEC determination and requiring structural re‐organization of the matrix and thus a minimum matrix flexibility. The use of bivalent cations for CEC determination may thus result in an overestimation of CEC for organic matter with low CEC. This has, however, promising potential when comparing CEC determined with monovalent cations and bivalent cations. Using a set of bivalent cations, may allow probing distribution of distances between functional groups in the organic matter and even characterize the matrix rigidity of the cation‐cross‐linked network.  相似文献   

17.
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   

18.
Data on accumulated exchangeable H, Al, Fe and Mn (Ma) cations in rock fractions in German soil profiles are scarce. The objective of this study was to describe the sum of accumulated Ma cations of fine earth and rock fragments in 11 deep soil profiles of varying genesis. Soil profiles were laid out at the sites Solling, Eifel, Harz mountains and the Erzgebirge and the parent materials included sandstones, siltstones, quartzite, slate, greywacke, diabase, gneiss and quartz porphyry. Exchangeable cations in the fine earth and rock fragments were measured in depths down to 6 m. Additionally, effective porosity and specific surface of rock fragments were determined. The effective porosity of the different rock fragments ranged from 4 to 28% (v/v), indicating that the rocks were accessible to solutions. For most samples, the cation exchange capacities (CEC) of the fine earth fractions were larger than those of the rock fragments, and the CEC (fine earth)/CEC (rock) ratios decreased with depth. All 11 profiles had small (<40%) amounts of exchangeable Na, K, Mg and Ca (Mb) cations in the fine earth fraction. Exchangeable Ma and Mb cations in the rock fragments changed similarly with depth as in the fine earth fractions for all profiles. Cumulative (rock + fine earth) Ma cations from 0—200 cm ranged from 474 to 1592 kmolc ha−1. The contribution of the rock fraction to the cumulative exchangeable Ma cations accounted for 13 to 85% of the total. The sum of exchangeable Ma cations was much higher than the cumulative acid deposition in western Germany since the beginning of industrialization, suggesting that carbonic acid and organic acids contributed largely to soil acidification. The rocks contribute significantly to buffering the acidity of the seepage water by silicate weathering and cation exchange. Therefore, acidification models which consider the fine earth fraction only, may lead to an overestimation of the rate of soil and groundwater acidification.  相似文献   

19.
The discharge of acidic mine drainage waters onto a hillslope in Dalarna, central Sweden, has lead to the contamination of the podzol soils with Cu, Fe, Ni, Pb, Zn and sulfate. Samples from contaminated and reference soils have been collected for chemical and mineralogical analyses. Jarosite is identified by x-ray diffraction analysis as a precipitate in the upper horizons (A, E, B) of the contaminated soils, where the soil acidity (pHKCl～2.6) promotes jarosite stability. The sequential chemical extraction of soil samples indicates that, in the reference A horizon, Cu, Pb, Ni and Zn are bound primarily to cation exchange sites and organic matter. In the A horizon of the contaminated soils closest to the rock dump, metal partitioning is dominated by the Fe oxide fractions, despite the high organic matter content; Pb is almost completely bound to crystalline Fe oxides, possibly adsorbed to Fe oxides or occuring in a jarosite solid solution. In the reference B and C horizons, Cu, Ni and Zn are primarily adsorbed/coprecipitated in the Fe oxide fractions, while Pb remains with a large fraction bound to organic matter. In the Fe-rich B horizon of the contaminated soils, the partitioning of the metals in cation exchange sites and to organic matter has greatly increased relative to the reference soils, resulting from the mobilization of organo-metal complexes down the profile.  相似文献   

20.

Background

Cation exchange capacity (CEC) is a routinely measured soil fertility indicator. The standard NH4OAc (pH 7) extraction procedure is time-consuming and overestimates actual CEC values of variable charge soils. Unbuffered extractants have been developed to measure the effective CEC (eCEC), but they differ in the type of index cation and extraction procedures.

Aim

This study was set up to systematically compare CEC values and exchangeable cation concentrations among different procedures and evaluate their practical aspects.

Methods

Five procedures were compared for (e)CEC, that is, silver thiourea (AgTU), cobalt(III) hexamine (Cohex), compulsive exchange (CE, i.e., BaCl2/MgSO4), BaCl2 (sum of cations in single-extract), and NH4OAc (pH 7). We applied these methods to a set of 25 samples of clay minerals, peat, or samples from soils with contrasting properties.

Results

The CEC values correlated well among methods (R2 = 0.92–0.98). Median ratios of eCEC (AgTU as well as CE) to the corresponding eCEC (Cohex) value were 1.0, showing good agreement between eCEC methods, but NH4OAc exceeded Cohex values (ratios up to 2.5 in acid soil). For BaCl2-extracteable cations, the ratio ranged from low (<1.0) in acid soils (acid cations not measured) to high (>1.0) in high-pH soil (dissolution of carbonates). Multiple-extraction methods (CE and NH4OAc) yielded more variation and increased labor.

Conclusions

The chemical properties of the sample cause method-specific interactions with chemical components of extractants. We found the Cohex method with ICP-MS detection to be the most efficient and cost-effective technique for determination of eCEC and exchangeable cations.  相似文献   

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