Contribution of Organic Matter to the Cation Exchange Capacity of Soils

Nature ◽  
1965 ◽  
Vol 207 (4997) ◽  
pp. 667-668 ◽  
Author(s):  
M. SCHNITZER
2013 ◽  
Vol 5 (4) ◽  
Author(s):  
Nenad Tomašić ◽  
Štefica Kampić ◽  
Iva Cindrić ◽  
Kristina Pikelj ◽  
Mavro Lučić ◽  
...  

AbstractThe adsorption properties in terms of cation exchange capacity and their relation to the soil and sediment constituents (clay minerals, Fe-, Mn-, and Al-oxyhydroxides, organic matter) were investigated in loess, soil-loess transition zone, and soil at four loess-soil sections in North-Western Croatia. Cation exchange capacity of the bulk samples, the samples after oxalate extraction of Fe, Mn and Al, and after removal of organic matter, as well as of the separated clay fraction, was determined using copper ethylenediamine. Cation exchange capacity (pH∼7) of the bulk samples ranges from 5 to 12 cmolc/kg in soil, from 7 to 15 cmolc/kg in the soil-loess transition zone, and from 12 to 20 cmolc/kg in loess. Generally, CEC values increase with depth. Oxalate extraction of Fe, Mn, and Al, and removal of organic matter cause a CEC decrease of 3–38% and 8–55%, respectively, proving a considerable influence of these constituents to the bulk CEC values. In the separated clay fraction (<2 μm) CEC values are up to several times higher relative to those in the bulk samples. The measured CEC values of the bulk samples generally correspond to the clay mineral content identified. Also, a slight increase in muscovite/illite content with depth and the vermiculite occurrence in the loess horizon are concomitant with the CEC increase in deeper horizons, irrespective of the sample pretreatment.


2012 ◽  
Vol 500 ◽  
pp. 142-148 ◽  
Author(s):  
Wen Xing Lü ◽  
Hong Jiang Zhang ◽  
Yu He Wu ◽  
Jin Hua Cheng ◽  
Jian Qiang Li ◽  
...  

Through the research and sampling analysis on different plant hedgerow in sloped farmland in Three Gorges reservoir area, we will conduct research on the impact of plant hedgerow in Three Gorges on the chemicophysical properties of soil and soil erosion. The results show that the plant hedgerow mainly composed by Morus alba, Citrus reticulata, Zanthoxylum bungeanum, Vitex negundoand Begonia fimbristipula can decrease the soil density as well as sand content and increase soil porosity, soil water content, silt content and clay content to some extent. The organic matter, nitrogen, phosphorus, potassium and cation exchange capacity and other chemical indices of soil in different locations in plant hedgerow indicate as maximum in on-band, minimum in inter-band, middle both upper-band and below-band. In the same slop with no plant hedgerow, the organic matter, nitrogen, phosphorus, potassium and cation exchange capacity and other chemical indices of soil show a trend of increasing from the top to the bottom of the slop, which reveals that these substances own a feature of accumulation by moving to the bottom. The strength of soil anti-corrosion in different plant hedgerow is: Vitex negundoand (79.2%)> Citrus reticulata (36.4%)> Morus alb (22.4%)> Zanthoxylum bungeanum (18.9%)> Begonia fimbristipula (15.3%)> CK (8.7%), and the soil anti-corrosion indices in plant hedgerow are decreasing with the increase of soil immersion time, besides, the former and the latter are 3 times polynomial function. For those 5 plant hedgerows, Vitex negundoand owns the best impact on improving soil chemicophysical properties and reducing soil erosion.


Soil Research ◽  
1994 ◽  
Vol 32 (5) ◽  
pp. 1015
Author(s):  
PW Moody

Krasnozems (Ferrosols) characteristically have high contents of citrate-dithionite extractable Fe and moderate to high contents of clay throughout the profile. They typically have low cation exchange capacity (2-20 cmolc kg-1), high P sorbing ability, and a significant anion exchange capacity at depth. The chemistry of krasnozems is dominated by the variable charge characteristics of the organic matter and the oxy-hydroxides of Fe and Al which occur in the predominantly kaolinitic clay fraction. The effects of surface charge characteristics, organic matter, and extractable iron and aluminium on the cation and anion exchange capacities, P sorbing abilities and pH buffer capacities of Australian krasnozems are reviewed. A selection of reports of nutrient deficiencies and toxicities in these soils is presented and briefly discussed. Published data on the chemical composition of the soil solutions of krasnozems are reviewed. Data from a suite of paired (undeveloped and developed) krasnozem profiles from eastern Australia indicate that exchangeable Ca and Mg, effective cation exchange capacity (ECEC), pH buffer capacity (pHBC) and total N decrease significantly (P < 0.05) in the A horizon following development, while exchangeable K, ECEC and pHBC decrease (P < 0-05) in the B horizon. The decreases in the A horizon are shown to be a direct consequence of the decline in organic matter which occurs following development. Because of the crucial role that organic matter plays in the chemical fertility of krasnozems, they are less likely to maintain their fertility under exploitative conditions than other productive clay soils such as Vertosols. It is concluded that the sustainable use of krasnozems will depend on maintenance or enhancement of organic matter levels, maintenance of surface and subsoil pH by regular application of amendments, minimization of erosion, and replacement of nutrients removed in harvested products.


2017 ◽  
Vol 29 (2) ◽  
pp. 123-131
Author(s):  
Reshma Akter ◽  
Md Jamal Uddin ◽  
Md Faruque Hossain ◽  
Zakia Parveen

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


1968 ◽  
Vol 48 (1) ◽  
pp. 53-63 ◽  
Author(s):  
J. S. Clark ◽  
W. E. Nichol

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.


1999 ◽  
Vol 79 (3) ◽  
pp. 501-504 ◽  
Author(s):  
B. J. Zebarth ◽  
G. H. Neilsen ◽  
E. Hogue ◽  
D. Neilsen

Sandy, infertile soils can benefit from the addition of organic waste amendments. Annual applications of organic wastes for as long as 4 yr increased soil organic matter content, decreased soil bulk density, and increased soil water retention of a coarse-textured soil. However, soil water-holding capacity was not necessarily increased, and there was a limited effect on soil cation exchange capacity. Key words: Cation exchange capacity, water retention, soil pH, soil organic matter, soil bulk density


1994 ◽  
Vol 74 (4) ◽  
pp. 421-429 ◽  
Author(s):  
Wietse L. Meyer ◽  
Paul A. Arp

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


1976 ◽  
Vol 56 (3) ◽  
pp. 213-221 ◽  
Author(s):  
Y. A. MARTEL ◽  
M. R. LAVERDIERE

The objectives of this work were (1) to determine the relation existing between the organic matter contents of Ap horizons and their respective soil Orders, (Gleysolic and Podzolic), texture, pH and geographic locations in the different thermal regions of Quebec and (2) to determine the role of organic matter and soil texture on the cation exchange properties of the same Ap horizons coming from soils used for forage crops in Quebec. The cation-exchange capacity (CEC), the exchangeable bases and acidity were determined by using 1 N NH4OAC – pH 7. The results showed a variation in the carbon content ranging from 1.4 to 6.9%. The heat units accumulated in each region and the clay contents were correlated with the percentage of carbon and nitrogen. Soil pH and soil Orders (Gleysolic vs. Podzolic) did not seem to affect the organic matter content. The cation-exchange capacity (CEC) ranged from 10.6 to 42.6 meq/100 g soil; 40% of this was attributable to carbon and 32% to clay contents. Simple and multiple regression equations showed that carbon was correlated with the exchangeable acidity, while clay was related to the exchangeable bases. The CEC of organic matter and clay were respectively 161 ± 45 meq/100 g organic matter and 29 ± 6 meq/100 g clay. These values, lower than for Western Canada, reflected the nature of the organic matter that is less developed in Eastern Canada than in the Chernozemic soils; they also showed the effect of the predominant illite mineral found in the clay fractions compared to montmorillonite in Western Canada.


Sign in / Sign up

Export Citation Format

Share Document