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1.
Abstract

Eight methods to determine exchangeable cations and cation exchange capacity (CEC) were compared for some highly weathered benchmark soils of Alabama. The methods were: (1) 1N NH4OAc at pH 7.0 by replacement (for CEC only), (2) 1N NH4OAc at pH 7.0 (summation of basic cations plus 1N KCl extractable Al), (3) 1N NH4OAc at pH 7.0 (summation of basic cations plus exchangeable H+), (4) 0.1M BaCl2 (summation of basic cations plus exchangeable Mn, Fe and Al), (5) Mehlich 1 (summation of basic cations plus 1N KCl extractable Al), (6) Mehlich 1 (summation of basic cations plus exchangeable H+), (7) Mehlich 3 (summation of basic cations plus 1N KCl extractable Al), and (8) Mehlich 3 (summation of basic cations plus exchangeable H+). The 0.1M BaCl2 was chosen as the standard method for the highly weathered soils and the other methods compared to it. The results indicated that the 1N NH4OAc replacement method gave significantly higher CEC values compared to the summation methods. This was probably due to the overestimation of the field CEC caused by measurement of pH dependent cation exchange sites in these soils. There was, however, close agreement between the BaCl2 method and the summation methods that included extractable Al. The generally good agreement between these summation methods suggests that the Mehlich 1 and Mehlich 3 extractants, commonly used to determine available nutrients in the southeastem USA, may also be used to measure effective CEC of some acid‐rich sesquioxide benchmark soils of Alabama. However, 1N KCl extractable Al as opposed to exchangeable H+ should be included in the computation.  相似文献   

2.

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   

3.
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   

4.
Abstract

Interpretation guidelines for the availability of calcium (Ca), magnesium (Mg), and potassium (K) in soilless media have been developed through plant growth studies and comparisons amongst extractants. The extractants used were 70% ethanol (EtOH), water, DTPA, ammonium acetate (NH4OAc) and silver thiourea (AgTu). Ethanol, which removes ions in pore water, extracted only 4.5, 13, and 26% of the Ca, Mg, and K, respectively, that could be extracted by AgTu from Pinus radiata bark of pH 5.66 and CEC of 11.2 cmol+/L. Acidification to pH 4.62 increased these proportions to 22, 40, and 38%. Correlations between water and DTPA for 39 media were excellent for both individual elements and the ratios Ca/Mg, K/Mg, and Ca, Mg, and K/(the sums of their concentrations in the extractants) (r2 = 0.88–0.98). Correlations between these extractants and AgTu and NH4OAc were poor for individual elements (r2 = 0.37–0.75) but high for ratios (r2 = 0.71–0.96). For Petunia ’Celebrity Salmon’ growing in peat media of similar pH but widely different Ca, Mg, and K proportions, the ratios of these elements in the shoots were highly correlated with their ratios in 2 mM DTPA extracts of the media. Similarly high correlations were obtained between the Ca/Mg ratios of the shoots of three Asplenium species growing in pinebark media and this ratio for DTPA, NH4OAc, and AgTu extracts of the media. The results indicate that the ratios of Ca, Mg, and K to one another in water and DTPA extracts of soilless media are good indicators of the availability of these elements to plants. Healthy specimens of the test plants grew in media whose DTPA extracts had a minimum Ca/Mg mole ratio of 1 or 2, depending on the Ca requirements of the species. The upper limit for good growth was deduced to be about 6. Limits for NH4OAc and AgTu extracts were similar to those found for crop plants in soils, at 1.6 or 3 to about 9. Minimum amounts of Ca, Mg, and K extracted by water and DTPA that were adequate for short‐term growth in the absence of further inputs were about 9,2.5, and 5 cmol+/L medium, respectively, at pH 6.0. The effect of pH on cations removed by water and DTPA raises the minima to about 19, 5, and 7.5 cmol+/L at pH 5.0.  相似文献   

5.
Abstract

Eighty four soil samples collected from southeastern Norway were analyzed for Cd by extraction with NH4OAc, DTPA, NH4OAc-EDTA, NH4NO3, HCl and CaCl2. The total Cd, pH, exchangeable K and Ca, dithionite-extractable Mn, available P and fine sand (0.2–0.02 mm) contents were the principal factors related to the extractable Cd, with some inter-extractant variations. Cadmium extracted by NH4NO3, NH4OAc, HCl and CaCl2 decreased with increasing soil pH, but the Cd extracted by all the extractants increased with increasing total Cd, exchangeable K and Ca, available P, and Mn-oxide contents in the soils. The Cd concentrations in plants were significantly related to the extractable Cd, exchangeable Ca and Mg, pH, Mn-oxides and organic matter content.  相似文献   

6.
Abstract

Comparisons of CEC and exchange acidity neasurements were made on a group of selected West African soils using three commonly used analytical procedures, namely, neutral‐acetate displacement, BaCl2‐TEA leaching at pH 8, and unbuffered KCl extraction.

The three methods gave large differences in CEC values which followed the order of BaCl2‐CEC>>NH4OAc‐CEC> KCl‐CEC. Results of exchange acidity also followed the same order. The high exchange acidity values obtained by the BaCl2‐TEA (pH 8) method were mainly due to changes in surface charge characteristics of Fe and Al oxides and hydrous oxides. The effective CEC method is recommended for routine soil analysis for highly weathered soils in the tropics.

Regression analysis of the base saturation values obtained from the three methods indicated the data followed a curvilinear relationship. The acetate method was more highly correlated with the effective CEC method than with the BaCl2 method.  相似文献   

7.
Abstract

An experiment was designed to evaluate several of the commonly used extractants and methods for determining “available”; elements in soils. The purpose of the study was to evaluate the suitability of these extraction procedures for use on forest soils typical for New England commercial forests. The extraction procedures selected included NH4OAc pH 4.8, NH4OAc pH 7.0, NH4Cl, Double Acid, Bray, and Mehlich methods. The elements measured varied somewhat by procedure but included the base cations, Al, Fe, Mn, and P. As a bioassay of element availability, a greenhouse study was conducted using six forest soil materials from different horizon types (i.e. O, Ap, B) and three conifer seedling species (red spruce, balsam fir, and white pine). Relatively small differences among extraction procedures were found among the methods used for exchangeable Ca, Mg, K, and Na. Large differences, however, were found among the different horizon types in the amount of exchangeable base cations present. In contrast, significant differences were found among extraction procedures for Al, Fe, Mn, and P depending on the degree of buffering and acidity of the extracting solution. Of the elements measured in this study, only P appeared to be growth limiting with the NH4OAc pH 4.8 being best correlated with P uptake by seedlings. Further work under field conditions over longer time periods is required to evaluate these methods for measuring P availability in forest soils  相似文献   

8.
Summary Methods of determining exchangeable K+ of soil by mixing extracting solutions and analysing the soil suspension with ion‐selective electrodes were developed and evaluated on 30 samples of soils. From preliminary comparisons of the K+ extracted by BaCl2 and NH4OAc solutions and by batch and leaching treatments of soils, we established that suspensions of 5 g soil in 100 ml 0.5 m BaCl2 and single batch treatments of 1 h should be used. The exchangeable K+ was determined with a K‐selective, valinomycin‐based PVC membrane electrode and electrochemical cells that did or did not include a liquid junction (the reference electrode being a double‐junction reference electrode assembly with a 10 m LiOAc salt bridge solution or a Cl‐selective electrode, respectively). The Ba‐exchangeable K+ values were sensibly the same whether a liquid junction was involved or not, a result that can be attributed to the beneficial effects of the salt bridge and the ionic strength of the extractant. Comparisons of these Ba‐exchangeable results with those obtained by various combinations of batch or leaching treatments, BaCl2 or NH4OAc extractants and filtrate analysis by the ion‐selective electrode method or atomic absorption spectrometry showed they were all highly correlated (r≥ 0.996). The selectivity of the K+‐selective electrode (kpotKNH4 = 0.004) significantly reduced the interference from indigenous soil NH4+ in the BaCl2 suspensions. Overall, the results show potentiometric measurements of K+ in soil suspensions can provide a simple, rapid, and reliable means of determining exchangeable K+ in soils.  相似文献   

9.
Abstract

Soil Samples (72) were collected from the Delta, Hill, and Northeast Blackland areas of Mississippi. Chemical analyses for manganese, magnesium, and calcium were made using the Mississippi Soil Test Solution (MSTS) and several other extracting solutions chosen for comparison. For the determination of available soil manganese, the MSTS proved to be as effective as either the Double Acid (0.025 N HCl in 0.05 N H2SO4) or 0.1 N H3PO4. The acid extractants removed more manganese than 1 N NH4OAc (pH 7.0) and therefore included forms that are not exchangeable. The methods studied for magnesium determinations were equilibrium extraction with 1 N NH4OAc, MSTS, Double Acid, 0.25 N CaCl2, and leaching with 1 N NH4OAc. All methods were highly correlated and therefore would be equally effective in determining available soil magnesium. Since MSTS and equilibrium extraction with 1 N NH4OAc removed similar amounts of magnesium from the soil, the same calibration can be used. Calcium determinations were made using equilibrium extraction with 1 N NH4OAc, MSTS, and Double Acid, and by leaching with 1 N NH4OAc. All methods proved effective in measuring available soil calcium on acid soils.  相似文献   

10.
Cation exchange is often studied with disturbed and dried soils, but the applicability of the results to undisturbed soils is not straightforward. We investigated the value of exchange coefficients obtained from standard procedures for predicting cation exchange in soil. Columns of undisturbed and disturbed subsoil of a Luvisol (SBt horizon) were leached under saturated conditions with 0.4, 4, 20, 41, 102 and 205 mm BaCl2 at a Darcy velocity of 1400 mm day?1. The model PHREEQC was used to calculate one‐dimensional transport, inorganic complexation and multiple cation exchange. Two model variants were tested: m1 (exchangeable cations obtained by percolation with NH4Cl) and m2 (exchangeable cations obtained by shaking the soil with BaCl2). The exchange coefficients (Gaines–Thomas formalism) were calculated from the ion activities in solution and exchangeable cations obtained by NH4Cl percolation (m1) or shaking with BaCl2 (m2). Variant m1 predicted cation exchange of the disturbed (homogenized) soil for the entire BaCl2 concentration range, whereas variant m2 resulted in a two‐fold overestimation of desorbed K for all experiments, which was related to large amounts of K released from the soil by shaking with BaCl2. In experiments with undisturbed soil, variant m1 predicted the concentrations of Mg, Ca, K, and Na in the solution phase and the sum of cations released from exchange sites. However, variant m2 predicted changes in ion concentrations and exchangeable cations somewhat less well. This study suggests that the amounts of exchangeable cations and exchange coefficients obtained from experiments with homogenized soil by percolation are useful to predict cation concentrations in column experiments with undisturbed soils.  相似文献   

11.
In upper mineral horizons, CEC by compulsive and isotopic exchange methods, using Ba2+ as the saturating cation, gave higher values than the effective CEC at natural soil pH, and much higher values than CEC determined with m NH4OAc at pH 7. Cumulative Al release during leaching was considerably higher using Mg2+ and Ba2+ chlorides than K+ and NH4+ chlorides, and gave a different shape extraction curve. Basal spacing of the dominant dioctahedral vermiculite in the soil clays contracted from 14.5Å to 10.0–10.9 Å when saturated with NH4+ and K+, restricting release of interlayer Al. Lower horizons, containing a large proportion of Al-chlorite in the clay fraction, which did not contract with any of the cations, showed more normal exchange behaviour. On leaching, Al release was slightly greater with K+ and NH4+, than with Mg2+ and Ba2+, chlorides. The implication of the results for CEC measurements is discussed.  相似文献   

12.
Most Brazilian soil-testing laboratories use Mehlich 1 and 1.0 M potassium chloride (KCl) solutions as extractants for the determination of phosphorus (P), potassium (K), and sodium (Na) and for exchangeable calcium (Ca), magnesium (Mg), manganese (Mn), and aluminum (Al) in agricultural soil samples. Other laboratories use a combination of exchangeable ionic resin and KCl procedures. With recent adoption of the inductively coupled plasma (ICP-OES) in routine soil-testing laboratories, soil extraction with 1.0 M ammonium chloride (NH4Cl) became an alternative due to the possibility of determining all exchangeable elements in one run (Ca, Mg, K, Mn, Na, and Al), leaving determination of phosphorus (P) with Mehlich 1 or exchangeable ionic resin. To evaluate the performance of the NH4Cl solution, an experiment was carried out with thirty-seven samples of soils representative of the southernmost state of Brazil, Rio Grande do Sul. Four extraction solutions [Mehlich 1 at soil/solution ratio of 1:10 and 1.0 M ammonium acetate (NH4OAc), 1.0 M KCl, and 1.0 M NH4Cl at soil/solution ratio 1:20] were used with three different shaking times (5, 30, and 60 min). Correlation coefficients among all methods were high. Mehlich 1 did not perform well against NH4OAc and NH4Cl, despite the high correlation coefficients, with values consistently lower for K, even when the time of extraction was increased from 5 to 30 or 60 min. However, for concentrations less than 0.30 cmol kg?1 (i.e., in the range of K deficiency), both solutions performed similarly. Calcium and Mg increased with time of shaking. Comparable values of exchangeable Ca, Mg, and K, as well as of Al and Mn, were obtained with 1.0 M NH4Cl with 60 min shaking and the standard procedures of 1.0 M NH4OAc and 1.0 M KCl. The determination of Al by traditional titration/back-titration of the 1.0 M KCl solution gave slightly greater results compared to ICP-OES obtained using extraction with 1.0 M NH4Cl. The results indicate that for Ca, Mg, Mn, and Al, it is possible to replace the traditional 1.0 M KCl extraction with 1.0 M NH4Cl solution, with 60 min shaking time and a soil/solution ratio of 1:20.  相似文献   

13.
Determination of the CEC of carbonate soils with unbuffered 0.1 M BaCl2 Soils containing carbonates and precipitated calcium carbonate, respectively, were percolated with unbuffered 0.1 M BaCl2 followed by 0.1 M MgCl2 and anorganic acids of the same concentration. The measured concentration of bases (including Ba++) in the percolates indicates, that precipitation of Ba++ or exchange with Ca++/Mg++ on carbonate surfaces occurs during percolation, which leads to an overestimation of exchangeable bases. From the total amount of Ba++ bounded in such a way the less part is dissolved/exchanged by MgCl2 solution in the following leaching step. So the CEC of carbonate soils seems to be generally overestimated too, by the method applied in a not exactly measurable degree.  相似文献   

14.
Abstract

Selected chemical properties of an artificially acidified agricultural soil from northern Idaho were evaluated in a laboratory study. Elemental S and Ca(OH)2were used to manipulate the soil pH of a Latahco silt loam (fine‐silty, mixed, frigid Argiaquic Xeric Argialboll), which had an initial pH of 5.7. A 100 day incubation period resulted in a soil pH manipulation range of 3.3 to 7.0. Chemical properties evaluated included: N mineralization rate, extractable P, AI, Mn, Ca, Mg and K and CEC. N mineralization rate (assessed by anaerobic incubation) decreased with decreasing soil pH. Nitrification rate also decreased as NH4 +‐N accumulated under acid soil conditions. Sodium acetate extractable P was positively linearly correlated (R2= 0.87) with soil pH over the entire pH range evaluated. Potassium chloride extractable Al was less than 1.3 mg kg‐1of soil at pH values higher than 4.4. Consequently, potential Al toxicity problems in these soils are minimal. Extractable Mn increased with decreasing soil pH. Soil CEC, extractable Mg, and extractable K all decreased with increasing soil pH from 3.3 to 7.0. Extractable Ca levels were largely unaffected by changing soil pH. It is likely that the availability of N and P would be the most adversely affected parameters by soil acidification  相似文献   

15.
Evaluation of nutrient status in soil is important for nutritional, environmental, and economical aspects. The objective of this work was to find out the most suitable universal extractant for determination of available phosphorus (P) and nitrate (NO3-) and exchangeable potassium (K), calcium (Ca), and magnesium (Mg) from soils using 0.01 M calcium chloride (CaCl2), 0.01 M barium chloride (BaCl2), 0.1 M BaCl2, 0.02 M strontium chloride (SrCl2), Mehlich 3, and ammonium bicarbonate diethylene triamine penta acetic acid (AB-DTPA) extractants. Composite surface soil samples (0–20 cm) were collected from the Eastern Harage Zone (Babile and Haramaya Districts), Wolaita Zone (Damot Sore, Boloso Bombe, Damot Pulasa, and Humbo Districts), and Dire Dawa Administrative Council by purposive sampling. The experiment was carried out in a completely randomized design (CRD) with three replications. Results indicated that the greatest correlations were found between Mehlich 3 and Olsen method and also between 0.02 M SrCl2 and Olsen method for available P. The amount of NO3– extracted by 0.02 M SrCl2 was significantly correlated to the amount determined by 0.5 M potassium sulfate (K2SO4). The amounts of exchangeable K, Ca, and Mg determined by ammonium acetate (NH4OAc) method were significantly correlated to the amount determined by universal extractants tested. In general, both 0.02 M SrCl2 and Mehlich 3 can serve as universal extractants for the macronutrients considered in this study with the former being more economical when NO3– is included.  相似文献   

16.
The fine earth (<2 mm) and rock fragments (>2 mm) fractions of two soils derived from Oligocene sandstone have been examined to assess the origin of the discrepancies between cation exchange capacity (CEC) and effective CEC (ECEC). The soils differ in terms of acidity: soil A is more acid than soil B. When the A samples are treated with BaCl2, the solution became sufficiently acid (pH < 4·5) to dissolve and to maintain Al in solution. From these samples more Al is released than base cations. Aluminium was continuously replenished even after 192 h, so that the ECEC was always larger than the CEC. Samples from soil B contain less H and Al ions, and the BaCl2 solution could not lower the pH below 5·0. In these samples little Al is released, and the base cations dominate the exchangeable pool of ions. This Al can be considered to be exchangeable, and a good agreement exists between the ECEC and the CEC. The source of non-exchangeable Al in the A samples is the OH-Al polymers of the hydroxy-interlayered vermiculite (HIV) and hydroxy-interlayered smectite (HIS) that tend to dissolve during the BaCl2 treatments. In the less acid B samples the Al polymers are not affected by BaCl2 treatment. Different results were obtained when the clays, extracted from an Na-dispersed suspension, were treated with BaCl2 solution. Because the clays are no longer acid, no H+ is released, and the OH-Al polymers are not dissolved. Therefore, the saturating ions play an important role in the dissolution of the OH-Al polymers and cause differences between the CEC and ECEC. We discount organic matter and specifically Al-organo complexes as a source of non-exchangeable Al. Both A and B soils contain very similar pyrophosphate-extractable Al, but show substantial differences in the amount of exchangeable Al.  相似文献   

17.
Abstract

The content of dissolved carbonates and exchanged acidity in triethanolamine‐buffered BaCl2‐solutions which were percolated through soil samples containing carbonates is determined by two titration‐procedures to pH 4.0 and 10.25. because a single titration value gives no information of the amounts of both ionic species in solution. The amount of dissolved carbonates calculated on the bases of these titration‐procedures, however, is smaller than that determined by measuring the content of inorganic carbon in solution. The difference is attributed to the sorption of protonized triethanolamine‐buffer during percolation, which leads to an underestimation of CEC when measured by re‐exchanged Ba++, whereas the amount of exchangeable bases is overestimated due to dissolution of carbonates. The amount of exchanged acidity calculated from the data obtained is surprisingly high and is at least partly attributed to the existence of HCO3 ‐ ‐sorbed on the surface of (wet) soils.  相似文献   

18.
Heats of adsorption and adsorption isotherms of ammonia gas were measured at 300 K (27 °C) on outgassed soil saturated with Na+, K+, NH4+, Ca2+, or Mg2+ ions. The Ca and Mg soils adsorbed apparently one more NH2 molecule per exchangeable ion than the Na and K soils, mostly in the relative pressure range o to 0.005, but not much more than the NH4 soil. The initial heat of adsorption was c. 75 kJ mol-1 on the Ca and Mg soils and c. 60 kJ mol-1 on the other soils. The results suggest that most NH, is sorbed on these soils through reactions not involving exchangeable cations.  相似文献   

19.
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   

20.
The charge characteristics of A1 or Ap and B2 horizon samples of total 23 Ultisols, Alfisols and Oxisols in Korea and Thailand were studied by measuring the retention of NH4+ and NO3? at different pH values (4–8) and NH4NO3 concentrations (0.1–0.005 m ). The magnitude of their negative charge (σ?; meq/100g) was dependent on pH and NH4NO3 concentration (C; m ) as represented by a regression equation: log σ?=apH +blogC +c. The values of the coefficient a (0.04–0.226), b (0.03–0.264) and c (–0.676–1.262) were correlated with the kinds of the soil and horizon and with the region where the soil exists. The retention of NO3? was less than 1 and 2–3 meq/100 g for the A1 or Ap and B2 horizon samples, respectively. The sum of exchangeable base and Al (‘effective’ CEC) was close to and higher than the magnitude of permanent charge (=σ? measured at pH = 4.3 and at C = 0.005 m ) for one-third and two-thirds of samples, respectively. A σ? value of 16 meq/100 g clay at pH = 7 and C = 0.01 m was found appropriate to separate the B2 horizons of Thai Ultisols and Oxisols from those of Korean Ultisols and Alfisols. Korean Alfisols and Ultisols and Thai Ultisols were distinguished from each other on the status of exchangeable base and Al  相似文献   

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