CATION EXCHANGE AND ASSOCIATED PROPERTIES OF SOME SOILS FROM VANCOUVER ISLAND, BRITISH COLUMBIA

1967 ◽  
Vol 47 (3) ◽  
pp. 187-202 ◽  
Author(s):  
J. S. Clark ◽  
A. J. Green ◽  
W. E. Nichol
Keyword(s):  
British Columbia ◽  
Organic Matter ◽  
Cation Exchange ◽  
Clay Content ◽  
Vancouver Island ◽  
Southeastern Part ◽  
Ph Dependent ◽  
High Base ◽  
Highly Correlated ◽  
Extractable Al

Studies of the cation exchange properties of the soils of Vancouver Island, British Columbia showed that, in general, the soils had high base saturation even though the precipitation was high. There was no consistent relation between the corrected lime potential values for the soils and the annual precipitation. The pH-dependent CEC values of the soils were highly correlated with organic matter and oxalate-extractable Al but poorer correlations were obtained with the clay content and oxalate-extractable Fe. The correlation between pH-dependent CEC and citrate-dithionite-extractable Fe was not significant. Complexes of Al with organic matter appeared to be the main source of the pH-dependent CEC in the soils.Soils from the drier southeastern part of the Island with fragipans had as low or lower corrected lime potential values in the upper part of the profile than did soils from the more humid and more densely forested parts of the Island. Although oxalate-extractable Al was accumulated in the upper solum of soils with fragipans there was no pronounced enrichment of either oxalate- or citrate-dithionite-extractable Fe. The corrected lime potential pattern and the free oxide distribution of the soils with fragipans differed from the soils without fragipans.

scholarly journals Adsorption of Fluometuron, Prometryne, Sencor, and 2,4-D by Soils

1969 ◽  
Vol 57 (4) ◽  
pp. 286-293 ◽  
Author(s):  
L. C. Liu ◽  
H. R. Cibes-Viadé
Keyword(s):  
Organic Matter ◽  
Cation Exchange ◽  
Adsorption Capacity ◽  
Cation Exchange Capacity ◽  
Organic Matter Content ◽  
Clay Content ◽  
Exchange Capacity ◽  
Matter Content ◽  
The Mean ◽  
Highly Correlated

The adsorption capacity of Fluometuron, Prometryne, Sencor, and 2,4-D by 48 local soils was determined spectrophotometrically. The mean adsorptivities of the four herbicides by these soils were as follows: Prometryne 37.0 percent, Sencor 23.0 percent, Fluometuron 22.6 percent, and 2,4-D 12.4 percent. The results indicated that organic matter content was the factor most highly correlated with adsorption of these herbicides by the 48 soils. Cation exchange capacity was found to correlate significantly with adsorption of Fluometuron, Prometryne, and Sencor. Such was not the case with 2,4-D. Correlation between clay content and adsorption of Fluometuron and Sencor was statistically significant. In contrast, no significant correlation was noted between clay content and adsorption of Prometryne and 2,4-D.

CLAY ILLUVIATION IN SOME ORTHIC PODZOLS OF EASTERN CANADA

1965 ◽  
Vol 45 (2) ◽  
pp. 127-138 ◽  
Author(s):  
J. E. Brydon
Keyword(s):  
Organic Matter ◽  
New Brunswick ◽  
Iron Oxides ◽  
Clay Content ◽  
Granular Structure ◽  
Charge Component ◽  
Eastern Canada ◽  
Free Iron ◽  
Fine Clay ◽  
Ph Dependent

The Arago, Barney, and Holmesville soils, Podzols from Quebec, Nova Scotia, and New Brunswick, respectively, each had friable Bfh horizons with moderate granular structure, and with organic matter and free Fe2O3 contents greater than the Ae and C horizons. The Arago and Holmesville had thin Bhft horizons containing over 10% organic matter and 5% free iron oxides. The C horizons of these two soils had some features characteristic of fragipans.The B horizons of the three soils had a high "pH-dependent charge component" in the C.E.C. values. The "permanent charge component" was similar throughout the Arago profile except for the Bhft horizon where clay accumulation had occurred.Translocation of clay from the Ae to the upper B horizons was indicated by the twofold increase in clay content and the relative enrichment of fine clay in the B horizons. Removal of free iron affected the clay contents differently in the different: horizons but the maximum clay content in the upper B horizons remained. The definitions of Orthic Podzols, Textural Podzols, and t horizons should be re-examined.

scholarly journals Relationship between soil oxidizable carbon and physical, chemical and mineralogical properties of umbric ferralsols

2011 ◽  
Vol 35 (1) ◽  
pp. 25-40 ◽  
Author(s):  
Flávio Adriano Marques ◽  
Márcia Regina Calegari ◽  
Pablo Vidal-Torrado ◽  
Peter Buurman
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Clay Content ◽  
Selective Extraction ◽  
Total Carbon ◽  
Soil Matrix ◽  
Soil Variables ◽  
Physical Chemical ◽  
Mineralogical Properties ◽  
Extractable Al

The occurrence of Umbric Ferralsols with thick umbric epipedons (> 100 cm thickness) in humid Tropical and Subtropical areas is a paradox since the processes of organic matter decomposition in these environments are very efficient. Nevertheless, this soil type has been reported in areas in the Southeast and South of Brazil, and at some places in the Northeast. Aspects of the genesis and paleoenvironmental significance of these Ferralsols still need a better understanding. The processes that made the umbric horizons so thick and dark and contributed to the preservation of organic carbon (OC) at considerable depths in these soils are of special interest. In this study, eight Ferralsols with a thick umbric horizon (UF) under different vegetation types were sampled (tropical rain forest, tropical seasonal forest and savanna woodland) and their macromorphological, physical, chemical and mineralogical properties studied to detect soil characteristics that could explain the preservation of high carbon amounts at considerable depths. The studied UF are clayey to very clayey, strongly acidic, dystrophic, and Al-saturated and charcoal fragments are often scattered in the soil matrix. Kaolinites are the main clay minerals in the A and B horizons, followed by abundant gibbsite and hydroxyl-interlayered vermiculite. The latter was only found in UFs derived from basalt rock in the South of the country. Total carbon (TC) ranged from 5 to 101 g kg-1 in the umbric epipedon. Dichromate-oxidizable organic carbon represented nearly 75 % of TC in the thick A horizons, while non-oxidizable C, which includes recalcitrant C (e.g., charcoal), contributed to the remaining 25 % of TC. Carbon contents were not related to most of the inorganic soil variables studied, except for oxalate-extractable Al, which individually explained 69 % (P < 0.001) of the variability of TC in the umbric epipedon. Clay content was not suited as predictor of TC or of the other studied C forms. Bulk density, exchangeable Al3+, Al saturation, ECEC and other parameters obtained by selective extraction were not suitable as predictors of TC and other C forms. Interactions between organic matter and poorly crystalline minerals, as indicated by oxalate-extractable Al, appear to be one of the possible organic matter protection mechanisms of these soils.

Surfactant Effects on Picloram Adsorption by Soils

Weed Science ◽  
1976 ◽  
Vol 24 (6) ◽  
pp. 549-552 ◽  
Author(s):  
J. D. Gaynor ◽  
V. V. Volk
Keyword(s):  
Organic Matter ◽  
Cationic Surfactant ◽  
Anionic Surfactant ◽  
Organic Matter Content ◽  
Clay Content ◽  
Surfactant Solution ◽  
Matter Content ◽  
Adsorption Sites ◽  
Surfactant Solutions ◽  
Extractable Al

The effects of soil organic matter, clay, extractable Al, cation exchange capacity, and pH on the adsorption of picloram (4-amino-3,5,6-trichloropicolinic acid) from aqueous and surfactant solutions were investigated. Linear adsorption isotherms for the soils were obtained with the Freundlich equation. Of the five soil properties investigated, Freundlich K values correlated with extractable Al and clay content. Picloram adsorption from aqueous solutions and from the non-ionic and anionic surfactant solutions was greater on the soils at pH 5 than at pH 7. The anionic surfactant competed with picloram for adsorption sites on the soils at pH 5. Picloram adsorption from solutions containing 0.1 and 1% cationic surfactant was greater than that from aqeuous and anionic and nonionic surfactant solutions. Picloram adsorption from the 10% cationic surfactant solution was similar on soils with pH 5 and 7 and increased with decreased organic matter content.

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.

A COMPARISON OF LIME REQUIREMENT METHODS FOR ACID CANADIAN SOILS

1977 ◽  
Vol 57 (3) ◽  
pp. 361-370 ◽  
Author(s):  
M. D. WEBBER ◽  
DIANE CORNEAU ◽  
P. B. HOYT ◽  
M. NYBORG
Keyword(s):  
British Columbia ◽  
Organic Matter ◽  
Soil Ph ◽  
Acid Soils ◽  
Toxic Level ◽  
Laboratory Methods ◽  
Exchangeable Al ◽  
Canadian Soils ◽  
Highly Correlated ◽  
Diagnostic Index

Several laboratory methods for estimating lime requirements of acid soils were compared using 24 soils from Alberta and northeastern British Columbia and 15 from elsewhere in Canada. The Peech, Schofield, Woodruff and SMP (Shoemaker et al. 1971) buffer methods were equally well correlated with lime requirements for raising soil pH to 5.5 or 6, which in turn were highly correlated with the amounts of soluble and exchangeable Al and organic matter in the soils. The SMP buffer method is recommended for use as the diagnostic index of lime requirement to achieve pH 5.5 or 6 because of its speed and simplicity. A refinement is suggested for Alberta and northeastern B.C. soils on the basis that lime need not be added to achieve pH 5.5 but should be added to reduce Al below the toxic level for sensitive crops. The lime requirements to reduce Al in those soils were highly correlated with the amounts of 0.02 M CaCl2-soluble Al they contained and it is recommended that the 0.02 M CaCl2-soluble AI be used as the diagnostic index of lime requirement. Lime requirements related to SMP (pH) and 0.02 M CaCl2-soluble Al are presented.

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

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

CHARACTERISTICS OF SOME LOAMY-TEXTURED PODZOLS IN NORTHEASTERN ONTARIO

1982 ◽  
Vol 62 (2) ◽  
pp. 281-290 ◽  
Author(s):  
L. J. EVANS
Keyword(s):  
Organic Matter ◽  
Cation Exchange ◽  
Mineral Soil ◽  
Internal Standard ◽  
Clay Mineralogy ◽  
Glacial Till ◽  
Soil Horizons ◽  
Ph Dependency ◽  
Ph Dependent ◽  
Forest Humus

Humo-Ferric Podzols (Typic Cryorthods) developed on glacial till or glaciolacustrine deposits were sampled in the Chapleau-Foleyet area of northeastern Ontario. pHs of Ae horizons ranged from 3.30 to 4.20 and of C horizons from 4.40 to 4.85. Cation exchange capacities (CEC) of mineral soil horizons averaged 1.7 meq/100 g, whilst those of the forest humus (fibrimors) averaged 166 meq/100 g. The CECs of the Bf and BC horizons were highly pH-dependent, averaging 3.2 meq/100 g at pH 4 and 16.8 meq/100 g at pH 8. The pH-dependency of CEC in these horizons was believed to be due to Al-complexes with organic matter. Calculated elemental loss using Zr as an internal standard showed significant losses of Mg, Fe, Ca and Al from Ae (albic) horizons and gains of Fe and, to a lesser extent, gains of Al in Bf (spodic) horizons. The clay mineralogy of Ae horizons was dominated by a high-charge smectite and that of Bf and BC horizons by chlorite.

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