DETERMINATION OF AVAILABLE PHOSPHORUS IN ACID AND CALCAREOUS SOILS WITH THE KELOWNA MULTIPLE-ELEMENT EXTRACTANT

Soil Science ◽  
1988 ◽  
Vol 146 (4) ◽  
pp. 284-291 ◽  
Author(s):  
W. VAN LIEROP
1989 ◽  
Vol 69 (2) ◽  
pp. 191-197
Author(s):  
W. VAN LIEROP

The objective of this study was to determine the effect of adding either 0.001M EDTA or 0.005M DTPA on the amount of P removed from acid and calcareous soils by the Kelowna and 0.25M HO Ac extractants. These complexing agents were studied for possible simultaneous extraction and determination of available Zn. To achieve that end, P-concentrations removed by these solutions from a group of acid, calcareous, and combined soils were compared against reference values obtained with 0.5M NaHCO3 (Olsen et al.) and the Kelowna extractant (0.25M HOAc + 0.015M NH4F) by means of graphing, correlation and regression techniques. Of the 80 soils studied, 40 were acid with pH (H2O) values ranging from 4.2 to 6.9 and the remainder having higher values up to 9.3. Results indicated that additions of either 0.001M EDTA or 0.005M DTPA to the Kelowna solution increased average extracted P concentrations by about 20 and 60%, respectively. Values removed by either of the new KEDTA and KDTPA solutions were closely related to those extracted with 0.5M NaHCO3 and Kelowna solutions on acid and calcareous soils (r values ≥ 0.96**). As EDTA and DTPA increased extracted soil P, these were added at 0.001 and 0.005M as NH4 preparations to 0.25M HOAc (AADTPA & AAEDTA; without fluoride), respectively, for determining whether these complexing agents could supplant F for P extraction. These solutions removed proportionally related amounts (r ≈ 0.94**) of P from calcareous, compared to the Kelowna and 0.5M NaHCO3 solutions, but relationships were less precise for acid soils (r ≈ 0.76**). These results suggest that the AADTPA or AAEDTA solution should be evaluated further before adoption for routine P determination in multiple element extractions. Key words: Mehlich in, acid soils, calcareous soils


1967 ◽  
Vol 50 (6) ◽  
pp. 1273-1279
Author(s):  
Gordon O Guerrant ◽  
J D Hunter ◽  
C H Mcbride

Abstract Available phosphorus has been determined in fertilizers by a quick extraction method useful for screening or quality control purposes. Samples were extracted in a Gooch crucible with a jet of 65 °C neutral ammonium citrate in 10—20 mill. A single direct determination of available phosphorus was made by the alkalimetric quimociac method, modified for speed and for use in high citrate concentrations. The results compare favorably in accviracy to the gravimetric quimociac results reported on 20 Magruder check fertilizer samples


1965 ◽  
Vol 48 (4) ◽  
pp. 859-865
Author(s):  
Wallace S Brammell

Abstract A simple, rapid spectrophotometry method has been developed for direct determination of available phosphorus in fertilizers. Citrate and other organic materials are destroyed by dry ashing. The combined water and citrate extracts are diluted, a 5 ml aliquot is pipetted into a 25 ml Erlenmeyer flask, and 2 ml of ashing reagent (dilute HNO3, sucrose, and MgO) is added. During evaporation to dryness on a hot plate, nonorthophosphates are hydrolyzed to orthophosphates which react with Mg to form heat-stable compounds. During the subsequent ashing, phosphorus remains in the ortho form. Due to sucrose, the dry residue has a very porous structure and can be converted to a white ash in about 30 minutes in a pre-heated 550°C muffle. Color is developed with vanadomolybdic acid reagent. Absorbance is read on a spectrophotometer at 400 mμ.


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