CONTRIBUTION OF EXCHANGEABLE ALUMINUM TO CATION EXCHANGE CAPACITY AT LOW pH

1987 ◽  
Vol 67 (1) ◽  
pp. 175-185 ◽  
Author(s):  
MARTIN DUQUETTE ◽  
WILLIAM H. HENDERSHOT
Keyword(s):  
Cation Exchange ◽  
Soil Ph ◽  
Cation Exchange Capacity ◽  
Exchange Capacity ◽  
Low Ph ◽  
Soil Samples ◽  
Maximum Amount ◽  
Exchangeable Al ◽  
Exchangeable Aluminum ◽  
Ph Dependent

The cation and anion exchange capacities (CEC and AEC) as functions of pH were measured for 12 soil samples from various parts of Quebec. In addition to the index cation Ca, Al was measured in the replacing solutions in order to evaluate the contribution of Al to pH-dependent CEC at low pH. Although all of the soils possessed some pH-dependent CEC, the soils with the steepest rise in CEC with pH were those with the largest accumulation of sesquioxides. The effective CEC, measured at the soil pH, ranged from 2.4 to 37.2 cmol(+) kg−1 while the CEC at pH 7 minus the CEC at pH3 varied from 4.4 to 39.9 cmol(+) kg−1. The maximum amount of exchangeable Al was found to correlate very highly with the amount of amorphous inorganic Al in the samples. The inclusion of exchangeable Al in the calculation did not significantly reduce the amount of pH-dependent CEC measured for the soils. Key words: Effective CEC, permanent charge, pH-dependent CEC

scholarly journals Crop Response to Soil Acidity Factors in Ultisols and Oxisols in Puerto Rico. XII. Tomatoes

1969 ◽  
Vol 69 (3) ◽  
pp. 357-365
Author(s):  
Edmundo Rivera ◽  
José Rodríguez ◽  
Fernando Abruña
Keyword(s):  
Puerto Rico ◽  
Cation Exchange ◽  
Soil Ph ◽  
Cation Exchange Capacity ◽  
Soil Acidity ◽  
Exchange Capacity ◽  
Crop Response ◽  
Exchangeable Al

The effect of acidity factors of two Ultisols and one Oxisol on yield and foliar composition of tomatoes was determined. Yields were not markedly reduced by acidity in the Ultisols until pH dropped to around 4.6 with 45% Al saturation of the cation exchange capacity (CEC), and no yield was produced at about pH 4.1 and 80% Al saturation. In the Oxisol, tomato yields dropped steadily from 39.7 t/ha, when there was no exchangeable AI, to 17.5 t/ha at the highest level of acidity, pH 4.4 and 43% AI saturation. In all soils, yields were closely correlated with soil pH, exchangeable Al and Ca and Al/Ca.

ETUDE SUR LA VALEUR DES CRITERES CHIMIQUES PROPOSES PAR LA COMMISSION PEDOLOGIQUE DU CANADA POUR LA CLASSIFICATION TAXONOMIQUE DES SOLS DU QUEBEC

1977 ◽  
Vol 57 (3) ◽  
pp. 233-247 ◽  
Author(s):  
ROGER W. BARIL ◽  
THI SEN TRAN
Keyword(s):  
Cation Exchange ◽  
Soil Ph ◽  
Classification System ◽  
Cation Exchange Capacity ◽  
Exchange Capacity ◽  
Taxonomic Classification ◽  
Single Test ◽  
Ph Dependent ◽  
Extractable Al

Correlations were made among chemical criteria used for taxonomic soil classificaton. The compared tests were: oxalate Δ (Fe + Al), pyrophosphate-extractable (Fe + Al), oxalate-extractable Al, pH-dependent cation exchange capacity (ΔCEC), ratios of pyrophosphate-extractable (Fe + Al) over clay or over dithionite-extractable (Fe + Al), and finally soil pH measured in 1 M NaF. Significant correlations were found among various measured parameters. However, no single test was found to be reliable as a single criterion when applied to the taxonomic classification of Quebec soils. The two chemical tests, pyrophosphate-extractable (Fe + Al) and its ratio over clay, combined with morphologic criteria appeared useful for classifying Quebec Podzols. A few soils, which presented discrepancies from chemical criteria were found difficult to classify, thus suggesting the possibility of establishing new sub-groups in the Canadain soil taxonomic classification system.

scholarly journals Influence of brick manufacturing on phosphorus and sulfur in different agro-ecological soils of Bangladesh

2017 ◽  
Vol 29 (2) ◽  
pp. 123-131
Author(s):  
Reshma Akter ◽  
Md Jamal Uddin ◽  
Md Faruque Hossain ◽  
Zakia Parveen
Keyword(s):  
Organic Matter ◽  
Cation Exchange ◽  
Soil Ph ◽  
Cation Exchange Capacity ◽  
Clay Content ◽  
Exchange Capacity ◽  
Soil Samples ◽  
Maximum Accumulation ◽  
Brick Kilns ◽  
Total P

A study was carried out to evaluate the effects of brick manufacturing on phosphorus (P) and sulfur (S) concentrations in soil and plant collected from different distances of brick kilns in four AEZs of Bangladesh. Forty eight composite soil samples (0 - 15 cm depth) were collected from 48 points in 12 different sites at 0 m, 300 m, 800 m and 1500 m from brick kilns, where most (site 2, site 3, site 5, site 6, site 7, site 9 and site 10) of the brick kilns used coal for brick burning purposes. Plant samples (rice straw and different vegetables) were also collected from the respective fields except 0 m distances. Significantly (p ? 0.05) lower organic matter, cation exchange capacity, clay content and soil pH were found at 0 m distances compared to other distances. Highest concentration of total P in soil were recorded at 0 m distances and these concentrations decreased with increasing distances from the brick kilns in most of the sites; whereas available P is significantly lower at 0 m distances than that of other distances. Total and available concentration of S in soil followed the trend 0 m>300 m>800 m>1500 m. Maximum accumulation of P (69.15 mg kg-1) and S (0.14%) in plant was found at 800 m away from the brick kiln.Bangladesh J. Sci. Res. 29(2): 123-131, December-2016

Surface charge characteristics and lime requirements of soils derived from basaltic, granite and metamorphic rocks in high rainfall tropical Queensland

Soil Research ◽  
1986 ◽  
Vol 24 (2) ◽  
pp. 173 ◽  
Author(s):  
GP Gillman ◽  
EA Sumpter
Keyword(s):  
Cation Exchange ◽  
Surface Charge ◽  
Soil Ph ◽  
Cation Exchange Capacity ◽  
Exchange Capacity ◽  
Exchange Method ◽  
High Rainfall ◽  
Exchangeable Al ◽  
Basaltic Soils ◽  
Highly Weathered Soils

The cation and anion exchange capacities of a large number of soils formed on basaltic, granitic, and metamorphic parent materials in the high rainfall area (approximately 4000 mm) of tropical north Queensland have been examined. Aspects studied included the changes in CEC and AEC between pH 4 and pH 6, the relative amounts of permanent and variable charge over this pH range, and the lime requirements of these highly weathered soils. A distinction is made between the Total Cation Exchange Capacity (CECT), defined as the Ca + Al adsorbed, and the Basic Cation Exchange Capacity (CECB), which is the Ca adsorbed. At low pH, CECB may be much less than CECT. The CEC, increase with pH in the highly oxidic basaltic soils is largely due to changes in surface charge, while in the granitic and metamorphic soils, increasing occupation of exchange sites by Al as pH decreases is the factor responsible for the increase in CECB. A good estimation of CECB at soil pH is obtained with a previously described compulsive exchange method, and there is high correlation between CECT at soil pH and the Effective Cation Exchange Capacity (= Ca + Mg + K + Na + Al). The amount of lime required to raise soil pH to pH 5.5 in the granitic and metamorphic soils was equivalent to the amount of exchangeable Al, but in the basaltic soils the lime requirement was two to three times greater than the amount of exchangeable Al.

Using pH-dependent CEC to determine lime requirement

2006 ◽  
Vol 86 (1) ◽  
pp. 133-139 ◽  
Author(s):  
Edouard Lemire ◽  
Kate M Taillon ◽  
William H. Hendershot
Keyword(s):  
Organic Matter ◽  
Soil Properties ◽  
Cation Exchange ◽  
Soil Ph ◽  
Cation Exchange Capacity ◽  
Soil Analysis ◽  
Organic Matter Content ◽  
Exchange Capacity ◽  
Ph Dependent ◽  
Ph Curve

Controlling soil pH is important to ensure good crop yield. This study was conducted to determine whether the accuracy of the existing Shoemaker-McLean-Pratt (SMP) pH-buffer method could be improved by using the pH-dependent cation exchange capacity curve (CECpd). Soil pH, SMP and CECpd measurements were performed on 18 acid surface horizon soil samples, with textures from sandy loam to clay loam. These soils were incubated with three levels of calcium carbonate for 12 wk, after which the soil pH and the effective cation exchange capacity (CECe) were measured. The correlation coefficient (R2) for the CECpd and CECe curves was 0.96. The main factor affecting the slope of the curves is the soil organic matter content. The increase of CECe in the soil was also found to be directly proportional to the amount of lime applied, regardless of the type of soil. By using the slope of the Qv versus pH curve for each soil and the relationship between CECe and lime application, we were able to determine the lime required to raise the soil pH in water to 6.5. As an alternative to the current practice of using the SMP buffer, we propose that it should be possible to estimate the pH-dependent CEC curve from measurable soil properties (e.g., organic matter) and to estimate the lime requirement as the difference in CECpd between the existing and desired pH values. Once the slope of the Qv/pH relationship has been determined or estimated for a soil, the only measurement necessary for calculating lime requirement in subsequent years would be the soil pH. The proposed method would provide lime requirement estimates while decreasing the annual cost of soil analysis. Key words: Lime requirement, cation exchange capacity, Non-Ideal Competitive Adsorption, soil properties, organic matter, Fe oxides

scholarly journals Influence of long-term mineral fertilization on metal contents and properties of soil samples taken from different locations in Hesse, Germany

SOIL ◽  
2015 ◽  
Vol 1 (1) ◽  
pp. 23-33 ◽  
Author(s):  
S. Czarnecki ◽  
R.-A. Düring
Keyword(s):  
Cation Exchange ◽  
Cation Exchange Capacity ◽  
Agricultural Soils ◽  
Mineral Fertilizer ◽  
Fertilizer Application ◽  
Exchange Capacity ◽  
Soil Samples ◽  
Residual Effects ◽  
Metal Contents

Abstract. Essential and non-essential metals occur in soils as a result of weathering, industrial processes, fertilization, and atmospheric deposition. Badly adapted cultivation of agricultural soils (declining pH value, application of unsuitable fertilizers) can enhance the mobility of metals and thereby increase their concentrations in agricultural products. As the enrichment of metals in soils occurs over long time periods, monitoring of the long-term impact of fertilization is necessary to assess metal accumulation in agricultural soils. The main objective of this study was to test the effects of different mineral fertilizer variations on soil properties (pH, Corg, and cation exchange capacity (CEC)) and pseudo-total and mobile metal contents of soils after 14 years of fertilizer application and to determine residual effects of the fertilization 8 years after cessation of fertilizer treatment. Soil samples were taken from a field experiment which was carried out at four different locations (210, 260, 360, and 620 m above sea level) in Hesse, Germany. During the study, a significant decrease in soil pH and an evident increase in soil carbon content and cation exchange capacity with fertilization were determined. The CEC of the soils was closely related to their organic C contents. Moreover, pseudo- and mobile metal (Cd, Cu, Mn, Pb, Zn) contents in the soils increased due to application of 14 years of mineral fertilizer treatments (N, P, NP, and NPK) when compared to control plots. Eight years after termination of the fertilization in the soil samples taken from soil profiles of the fertilized plots (NPK) for monitoring the residual effects of the fertilizer application, a decrease of 82.6, 54.2, 48.5, 74.4, and 56.9% in pseudo-total Cd, Cu, Mn, Pb, and Zn contents, respectively, was determined.

ESTIMATION OF THE INORGANIC AND ORGANIC pH-DEPENDENT CATION EXCHANGE CAPACITY OF THE B HORIZONS OF PODZOLIC AND BRUNISOLIC SOILS

1968 ◽  
Vol 48 (1) ◽  
pp. 53-63 ◽  
Author(s):  
J. S. Clark ◽  
W. E. Nichol
Keyword(s):  
Organic Matter ◽  
Cation Exchange ◽  
Cation Exchange Capacity ◽  
Acid Soils ◽  
Exchange Capacity ◽  
Hydrous Oxides ◽  
Before And After ◽  
Ph Dependent ◽  
The Difference ◽  
Wyoming Bentonite

Heating in hydrogen peroxide, dilute oxalic acid, and dilute aluminum oxalate did not change the effective cation exchange capacity (CEC) or the pH-7 CEC of Wyoming bentonite and Alberni clay soil containing excess Al(OH)x. This indicated that treatment of soils with H2O2 to oxidize organic matter and the possible production of oxalates during oxidation did not change the CEC values of the inorganic fraction of soils even if some clay exchange sites were blocked by hydrous oxides of Al.With soils of pH less than approximately 5.4, oxidation of organic matter did not change the effective CECs although the pH-7 CEC values were decreased. Thus, organic matter in acid soils appeared to have little or no effective CEC. Because of this and the negligible effect of H2O2 oxidation on the CEC values of clays, the difference of the pH-7 CEC of soils before and after H2O2 oxidation provided a simple means of estimating the amount of organic pH-dependent CEC in acid soils.The amount of organically derived pH-dependent CEC was determined in a number of soils by means of peroxide oxidation. The technique provided a useful indication of the quantities of sesquioxide–organic matter complexes accumulated in medium- and fine-textured soils.

Exchangeable cations and cation exchange capacity of forest soil samples: Effects of drying, storage, and horizon

1994 ◽  
Vol 74 (4) ◽  
pp. 421-429 ◽  
Author(s):  
Wietse L. Meyer ◽  
Paul A. Arp
Keyword(s):  
Organic Matter ◽  
Cation Exchange ◽  
Cation Exchange Capacity ◽  
Storage Time ◽  
Ammonium Acetate ◽  
Exchange Capacity ◽  
Soil Samples ◽  
Storage Effects ◽  
And Storage ◽  
Extractable Al

Concentrations of Ca, Mg, K, Na, Al, Fe, Mn, and Si extractable with 1 N ammonium chloride (NH4Cl, pH 4.5) and 1 N ammonium acetate (NH4OAc, pH 4.5) were determined for forest soil samples as follows: (1) before drying, and (2) at several time intervals after air-drying (1, 5, 11 and 14 wk). Values for CEC were obtained for the same samples by determining (1) the sum of cations (Al3+, Ca2+, Mg2+, K+, Na+, Fe3+, and Mn2+) in the extracts [denoted [Formula: see text] and [Formula: see text]], and (2) the amount of ammonium retained by the soil samples against water washing [denoted CEC(NH4OAc) and CEC (NH4Cl)]. The soils used in this investigation were taken from four New Brunswick upland forest sites (two sugar maple sites, one mixed wood site, and one spruce site). It was round that (1) extractable Mg, K, Na, and Mn levels were generally not affected by drying, storing, and type of extradant; (2) extractable Al and Fe levels increased immediately after drying; (3) NH4OAc-extracted Al, Fe, and Si exceeded NH4Cl-extracted Al, Fe, and Si; (4) extracted Al and Fe levels tended to drop after 11 wk of storage; (5) small drying effects were also noticed for NH4Cl-extracted Ca; (6) CEC(NH4OAc) and CEC(NH4Cl) values decreased with increasing time of storage; this effect was noticed most for soil samples with high levels of organic matter (Ah, Ahe, Bm, Bf, and Bfh), and was noticed least for sod samples taken from leached horizons (Ae) and subsoil horizons (BC and C); (7) in some cases, storage time increased CEC(NH4OAc) in subsoils; (8) values for [Formula: see text] remained fairly independent or increased slightly with storage time and were closely related with CEC(NH4Cl) values obtained with non-dried samples; (9) values for [Formula: see text] did not relate well with CEC(NH4OAc) and CEC(NH4Cl). Differences for extractable Al were likely due to Al complexation by acetate ions. Drying effects on extractable Al and Fe (and possibly Ca) were likely due to drying-induced fragmentation of soil organic matter. Drying and storage effects on CEC(NH4OAc) and CEC(NH4Cl) were likely due to (1) water-washing and related loss of organic matter, and (2) sensitivity of subsoil minerals to air exposure. Apparent drying and storage effects on CEC were most noted with [Formula: see text] and were least noted with [Formula: see text]. Key words: Cation exchange capacity, ion exchange, drying, storage, ammonium acetate, ammonium chloride extractions

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