1952
DOI: 10.1097/00010694-195204000-00001
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Exchangeable Cation Analysis of Saline and Alkali Soils

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Cited by 530 publications
(195 citation statements)
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“…The determination of the physico-chemical properties was carried out in duplicate on the <100 urn size fraction: Soil pH and electrical conductivity were measured in 1:2 and 1:5 soil/water extracts, respectively, oxidisable organic matter content was determined using the Walkley-Black method (Walkley 1935), calcium carbonate was determined with the calcimeter Bernard method (Allison and Moodie 1965), and cation exchange capacity was evaluated with 1 N ammonium acetate (Bower et al 1952). Analyses of the WEPAL ISE 987 standard yielded results that were 116, 102 and 90 % of the certified values for oxidisable organic matter, pH and calcium carbonate, respectively.…”
Section: Methodsmentioning
confidence: 99%
“…The determination of the physico-chemical properties was carried out in duplicate on the <100 urn size fraction: Soil pH and electrical conductivity were measured in 1:2 and 1:5 soil/water extracts, respectively, oxidisable organic matter content was determined using the Walkley-Black method (Walkley 1935), calcium carbonate was determined with the calcimeter Bernard method (Allison and Moodie 1965), and cation exchange capacity was evaluated with 1 N ammonium acetate (Bower et al 1952). Analyses of the WEPAL ISE 987 standard yielded results that were 116, 102 and 90 % of the certified values for oxidisable organic matter, pH and calcium carbonate, respectively.…”
Section: Methodsmentioning
confidence: 99%
“…Each layer from each pit was sampled and analysed. The following parameters were evaluated: Percentage (w/w) of Clay, Loam and Sand in the soil fraction < 2 mm by Robinson's pipette method according to Gee and Bauder (1986) and texture taxonomy by United States Department of Agriculture (USDA); Percentage of coarse elements with diameter > 2 mm (Ө, w/w); Soil moisture at Field Capacity (FC, % w/w) and at Permanent Wilting Point (PWP, % w/w) by comparing the weights of dry and wet soil under suction pressure of 0.3 and 1.5 MPa, respectively (according to Miller and Gardiner, 1998), using vacuum machines by Eijkelkamp Agrisearch Equipment BV (Giesbeek, Holland), after separating course elements; Bulk Density (r, g cm -3 ) by excavation method (according to Blake and Hartge, 1986) and Thickness (H, m); Useful Water Reserve (UWR, mm) by calculation UWR = (FC-PWP)*(100-Ө)*H* r; pH (ratio 1:2.5); Electric Conductivity (ratio 1:5, 25 ºC, dS m -1 ); Total Organic Matter (MOT, % w/w) by determination of the Oxidable Organic Carbon (COO) (titration with iron sulphate (FeSO 4 ) of the excess of potassium dichromate (K 2 Cr 2 O 7 )) and calculation MOT = COO*1.29*1.72 (being 1.29 and 1.72 the recuperation coefficient and the Van Bemmelen conversion coefficient, respectively) according to Porta et al (1986); Total Nitrogen (% w/w) following Kjeldahl digestion as described by Bremmer and Mulvaney (1986); Available Phosphorous (mg kg -1 ) according to Olsen method (1954); Total Carbonate (% w/w) and Calcium Carbonate Equivalent (% w/w) by reaction with hydrogen chloride (HCl) and measurement of carbon dioxide (CO 2 ) according to the method of Bernard calcimeter as described by Porta et al (1986); Exchangeable calcium (Ca ++ , mmol kg -1 ), magnesium (Mg ++ , mmol kg -1 ), potassium (K + , mg kg -1 ) and sodium (Na + , mg kg -1 ) by atomic absorption spectrophotometry as described by Rowell (1996); Cationic Exchange Capacity (mmol kg -1 ) by saturation with ammonium acetate (CH 3 COONH 4 ) (Bower et al, 1952).…”
Section: Methodsmentioning
confidence: 99%
“…Particle-size analysis: hydrometer method (Gee and Bauder 1986); calcium carbonate equivalents (CCE): back titration procedure (Leoppert and Suarez 1996); soil pH and electrical conductivity (EC): 1:2 soil: water extract after shaking for 30 min (Hesse 1971); organic carbon (OC): dichromate oxidation and titration with ferrous ammonium sulfate (Walkley and Black 1934); total nitrogen (TN): Kjeldahl method (Hinds and Lowe 1980); cation-exchange capacity (CEC): according to Bower et al (1952); available phosphorus: extraction with 0.5M NaHCO 3 (pH 8.5) and determination spectrophotometrically as blue molybdate-phosphate complexes under partial reduction with ascorbic acid (Jackson 1958).…”
Section: Methodsmentioning
confidence: 99%