LABILE RESIDUAL FERTILIZER PHOSPHORUS IN CHERNOZEMIC SOILS. I. SOLUBILITY AND QUANTITY/INTENSITY STUDIES

1977 ◽  
Vol 57 (1) ◽  
pp. 65-73 ◽  
Author(s):  
J. M. SADLER ◽  
J. W. B. STEWART

Granular monoammonium phosphate (500 μg P/g soil) was applied in the field to three soils of an Oxbow catena. Changes in the inorganic P forms controlling P concentration or intensity (Ie) in soil solution during the ensuing 2½ yr were determined by equilibrium solubility product and related quantity/intensity analyses. In the Calcareous and Orthic control soils, Ie was controlled by impure hydroxyapatite. After P addition, it was controlled by dicalcium phosphate dihydrate and octocalcium phosphate. Marked changes in the quantity of labile P caused negligible changes in values for Ie. Therefore, in these and similar Chernozemic soils, Ie should adequately reflect the availability of residual P to plants. In the Gleysol after P addition, Ie was determined by adsorbed P or by the solubility of aluminum/iron-bound P forms. For this and similar Chernozemic soils, the quantity/intensity data indicated that estimates of the availability of residual P will require a measurement of its capacity to maintain Ie at the root–soil interface against depletion by plant uptake rather than a measurement of Ie alone.

2000 ◽  
Vol 9 (1) ◽  
pp. 61-70 ◽  
Author(s):  
R. UUSITALO ◽  
H.-R. TUHKANEN

The aim of this study was to test whether phosphorus saturation of surface sorption sites of (oxyhydr)oxides of aluminium (Al) and iron (Fe) in Finnish soils can be assessed using a single oxalate extraction and, if so, whether the results are closely related to the P forms likely to influence the P concentration in runoff waters. Ten soil samples with varying clay content and P status were studied. Desorption tests were conducted by submitting the soils sequentially to nine anion exchange resin (AER) extractions. Sorption of P was studied by shaking the soils in P standard solutions (0-250 ppm). Soil inorganic P was characterised by sequentially extracting P from the fractions assumed to be connected to Al and Fe compounds and present as the stable apatitic form. The desorption studies and the fractioning of inorganic P suggested that oxalate solution dissolves apatitic P and/or other relatively stable P-bearing compounds, probably referring to the sum of inorganic P fractions rather than labile P. The amount of P desorbed in the nine AER extractions was about 80-280 mg/kg, whereas oxalate extracted about 490-1100 mg P/kg, which approximated the sum of the inorganic P fractions. Therefore, in soils high in apatitic P, oxalate-extractable P does not seem to be a reliable measure of the P saturation of Al and Fe oxide surfaces that regulate the P concentration in soil solution and runoff water.;


Soil Research ◽  
2007 ◽  
Vol 45 (7) ◽  
pp. 524 ◽  
Author(s):  
X. Wang ◽  
D. W. Lester ◽  
C. N. Guppy ◽  
P. V. Lockwood ◽  
C. Tang

Long-term removal of grain P and soil test data suggested that the Colwell phosphorus (P) extraction from the surface 0.10 m of a Black Vertosol from south-eastern Queensland was a poor indicator of run-down of soil P pools. We proposed that plants were also accessing P from layers below 0.10 m or from surface soil P pools not extracted by the Colwell extraction. Both topsoil and subsoil samples in 1994 and 2003 were collected from nil and 20 kg P/ha per crop treatments in a long-term N × P field experiment established in 1985 for detailed P fractionation. An uncropped reference soil was also taken in 2003 from an adjacent area. The long-term effect of the field treatments on soil P fractions was evaluated by comparing the reference site, which was assumed to represent the original soil condition, to the 2003 samples. Without addition of P fertiliser, 55%, 35%, and 10% of total P removal were from 0 to 0.10, 0.10 to 0.30, and 0.30 to 0.60 m, respectively, compared with the uncropped reference soil. Labile fractions comprising resin, bicarbonate, and hydroxide pools in the top 0.10 m decreased by approximately 60% and accounted for 15% of the total P decrease from 0 to 0.60 m depth. Acid and residual-P fractions decreased by 50% and 20%, respectively, and accounted for ~20% and 15% of the total P decrease. In contrast, P addition at 20 kg P/ha per crop over 18 crops doubled the resin and bicarbonate inorganic P (NaHCO3-Pi) pools in the surface 0.10 m. Hydroxide (NaOH-Pi) and acid extracted inorganic P increased by 25% and 10%, respectively, while the residual-P pool decreased by about 15%. Below 0.10 m, very little P was removed by the first 3 extractants. Most of the P was present in the acid and residual fractions irrespective of fertiliser application. The acid and residual-P dropped by 30% and 12%, respectively, at 0.10–0.30 m and 12% and 8% at 0.30–0.60 m. When comparing the experimental soil samples in 2003 with those in 1994, similar trends were observed in the changes of each soil P fraction. In the surface 0.10 m, acid and residual-P pools decreased greatly and explained almost all of the total P decrease in the surface soil without P input. With P addition, labile pools acted as the main sink for P. The acid pool increased by 7%, while the residual-P showed a decrease in the topsoil. Total P level was elevated noticeably in this soil layer. However, at 0.10–0.30 m depth, acid and residual pools were the dominant fractions and decreased significantly irrespective of P fertiliser addition. Below 0.30 m, no significant changes were detected for each fraction and total P. The results suggest that crops had accessed significant amounts of P at 0.10–0.30 m depth irrespective of P fertiliser application, and that subsoil sampling (0.10–0.30 m) should be considered in order to improve the monitoring of soil P status. However, choice of appropriate extractants for monitoring subsoil P reserves is yet to be undertaken.


Agronomy ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 248
Author(s):  
Tanabhat-Sakorn Sukitprapanon ◽  
Metawee Jantamenchai ◽  
Duangsamorn Tulaphitak ◽  
Nattaporn Prakongkep ◽  
Robert John Gilkes ◽  
...  

Understanding phosphorus (P) dynamics in tropical sandy soil treated with organic residues of contrasting quality is crucial for P management using organic amendments. This research determined P fractions in a tropical sandy soil under the application of organic residues of different quality, including groundnut stover (GN), tamarind leaf litter (TM), dipterocarp leaf litter (DP), and rice straw (RS). The organic residues were applied at the rate of 10 t DM ha−1 year−1. The P fractions were examined by a sequential extraction procedure. Organic residue application, regardless of residue quality, resulted in P accumulation in soils. For unamended soil, 55% of total P was mainly associated with Al (hydr)oxides. Organic residue application, regardless of residue quality, diminished the NH4F-extractable P (Al-P) fraction, but it had a nonsignificant effect on NaOH-extractable P (Fe-P). The majority of Al-P and Fe-P fractions were associated with crystalline Al and Fe (hydr)oxides. NH4Cl-extractable P (labile P), NaHCO3-extractable P (exchangeable P and mineralizable organic P), HCl-extractable P (Ca-P), and residual P fractions in soil were significantly increased as a result of the incorporation of organic residues. The application of organic residues, particularly those high in ash alkalinity, increase soil pH, labile P, and Ca-P fractions. In contrast, applications of residues high in lignin and polyphenols increase residual P fraction, which is associated with organo-mineral complexes and clay mineral kaolinite.


1986 ◽  
Vol 66 (1) ◽  
pp. 105-119 ◽  
Author(s):  
B. I. WAGAR ◽  
J. W. B. STEWART ◽  
J. O. MOIR

A sequential phosphorus (P) fractionation procedure was used to measure the changes in the labile and stable forms of inorganic and organic P following single broadcast P applications to Canadian Chernozemic soils under cereal cropping. Approximately half of the fertilizer residues remained in plant-available forms (resin, NaHCO3). In a Black Waskada clay loam 8 yr after the application of 200 and 400 kg P ha−1, residual fertilizer P consisted of resin-P, 30–40%; HCl-P, 25–30%; residue-P, 10–15%; NaOH-P, 10–15%, NaHCO3-P, 10%; and aggregate protected P, 3%. The residues in a Dark Brown Sutherland clay 5 yr after the application of 160 kg P ha−1 were: resin-P, 35%; NaOH-P, 30–40%; NaHCO3-P, 15%; HCl-P, 0–5%; H2SO4-P, 5%; and aggregate protected P, 5%. The soils differed in the quantity of fertilizer recovered in inorganic HCl-extractable forms. In the Sutherland soil the change from wheat-fallow to continuous wheat cropping produced a build-up of organic P which occurred with and without the addition of P fertilizer. Key words: Residual P, P transformations, Labile Pi; labile Po, stable Pi stable Po


2015 ◽  
Vol 12 (21) ◽  
pp. 6443-6452 ◽  
Author(s):  
X. Jiang ◽  
R. Bol ◽  
S. Willbold ◽  
H. Vereecken ◽  
E. Klumpp

Abstract. To maximize crop productivity fertilizer P is generally applied to arable soils, a significant proportion of which becomes stabilized by mineral components and in part subsequently becomes unavailable to plants. However, little is known about the relative contributions of the different organic and inorganic P bound to Fe/Al oxides in the smaller soil particles. Alkaline (NaOH–Na2EDTA) extraction with solution 31P-nuclear magnetic resonance (31P-NMR) spectroscopy is considered a reliable method for extracting and quantifying organic P and (some) inorganic P. However, any so-called residual P after the alkaline extraction has remained unidentified. Therefore, in the present study, the amorphous (a) and crystalline (c) Fe/Al oxide minerals and related P in soil aggregate-sized fractions (> 20, 2–20, 0.45–2 and < 0.45 μm) were specifically extracted by oxalate (a-Fe/Al oxides) and dithionite–citrate–bicarbonate (DCB, both a- and c-Fe/Al oxides). These soil aggregate-sized fractions with and without the oxalate and DCB pre-treatments were then sequentially extracted by alkaline extraction prior to solution 31P-NMR spectroscopy. This was done to quantify the P associated with a- and c-Fe/Al oxides in both alkaline extraction and the residual P of different soil aggregate-sized fractions. The results showed that overall P contents increased with decreasing size of the soil aggregate-sized fractions. However, the relative distribution and speciation of varying P forms were found to be independent of soil aggregate-size. The majority of alkaline-extractable P was in the a-Fe/Al oxide fraction (42–47 % of total P), most of which was ortho-phosphate (36–41 % of total P). Furthermore, still significant amounts of particularly monoester P were bound to these oxides. Intriguingly, however, Fe/Al oxides were not the main bonding sites for pyrophosphate. Residual P contained similar amounts of total P associated with both a- (11–15 % of total P) and c-Fe oxides (7–13 % of total P) in various aggregate-sized fractions, suggesting that it was likely occluded within the a- and c-Fe oxides in soil. This implies that, with the dissolution of Fe oxides, this P may be released and thus available for plants and microbial communities.


2011 ◽  
Vol 322 ◽  
pp. 108-111 ◽  
Author(s):  
Bao Tong Huang ◽  
Hua Zhou ◽  
Huai Xiang Ding

A fifteen-year field trial (started in 1990) was conducted to determine the inorganic P fractions under 8 classical modes of fertilization in the lower reach of Liaohe River Plain. The results showed that Ca2-P, Ca8-P, Al-P and Fe-P decreased in the absence of P application, while increased with supplemental P addition. Interestingly, O-P and Ca10-P, with low bioavailability, increased at different levels under all treatments after 15 years. The contents of inorganic P were low in crop stalk, indicating that P supplying capacity was weak. On the contrary, both fresh pig excretion and decomposed manure were huge inorganic P pools.


2009 ◽  
Vol 89 (1) ◽  
pp. 49-66 ◽  
Author(s):  
C. A. Grant ◽  
M. A. Monreal ◽  
R. B. Irvine ◽  
R. M. Mohr ◽  
D. L. McLaren ◽  
...  

Field studies were conducted over a 4-yr period at two locations in western Manitoba, Canada, to evaluate the effect of phosphorus (P) fertilizer management on crop growth as affected by tillage system through a 2-yr cropping sequence. In the first phase of the cropping sequence, canola (Brassica napus L.), a non-mycorrhizal crop, and spring wheat (Triticum aestivum L.), a mycorrhizal crop, were grown under conventional (CT) and reduced (RT) systems, with 0, 11 and 22 kg P ha-1 applied as monoammonium phosphate (MAP). In the second phase of the sequence, flax (Linum usitatissimum L.) was seeded following the spring wheat or canola, with application of 0 or 11 kg P ha-1 as MAP. Phosphorus application increased the early-season biomass, P concentration, and P accumulation of canola and wheat and the seed yield of canola. Tillage system had no consistent effects on growth, P concentration or uptake, or seed yields of canola or wheat, nor were P by tillage system interactions observed. Early-season biomass production and seed yields of flax were relatively unaffected by P fertilization whether applied in the same season as flax or in the previous season, although early-season P concentration and P accumulation were increased when P fertilizer was applied to the flax. Of the factors evaluated in this study, preceding crop had the greatest influence on flax growth with flax establishment, early-season biomass, and P accumulation, and seed yield all being significantly greater when flax was seeded after wheat than after canola. Key words: Crop rotation, fertilization, monoammonium phosphate, flax, wheat, canola


2000 ◽  
Vol 80 (4) ◽  
pp. 561-566 ◽  
Author(s):  
P. Qian ◽  
J. J. Schoenau

Limited information exists as to the short-term effect of liquid swine manure on P distribution in soil. To address this issue, forms and distribution of inorganic P (Pi) and organic P (Po) at 2 wk and 16 wk after manure addition were investigated through a sequential extraction procedure. An Orthic Black Chernozem was sampled from a field research plot (Dixon, SK) without previous manure and urea additions. Liquid swine manure and urea were applied at rates of 0, 100 and 400 mg N kg−1, corresponding 10 and 40 mg P kg−1 from manure. Manure addition did not increase the most labile P fractions in soil. Instead the initial fate of the P from the manure was mainly to enter moderately labile and stable fractions such as calcium phosphate and organic P forms. This is consistent with observations in the field that a single application of swine effluent does not have a large impact on extractable "available" P in the soil. Further studies are needed to determine how much manure P loading is required for saturation of the "fixed pool" of P in Saskatchewan soils. Key words: Phosphorus fractions, sequential P extraction, incubation, urea, swine manure, anion exchange membrane


Author(s):  
L.M. Condron ◽  
K.M. Goh

Changes in soil phosphorus (P) associated with the establishment and maintenance of improved ryegrass-clover pasture under different superphosphate fertiliser treatments were examined over a 20-year period (1957-77). Results showed that soil organic P increased with increasing applications of P fertiliser. This represents a dynamic balance between rates of organic P addition and breakdown in the soil. This balance is reached slowly and may be significantly altered only by drastic changes in land use. In annually fertilised soils, amounts of inorganic P increased with time. However, the potential utilisation of this residual inorganic P is limited by its apparent stability in the soil. Keywords grazed pasture, irrigation, fertiliser P, soil inorganic P, soil organic P, soil P fractionation


1962 ◽  
Vol 42 (2) ◽  
pp. 229-239 ◽  
Author(s):  
W. C. Hinman ◽  
J. D. Beaton ◽  
D. W. L. Read

Pre-weighed monocalcium phosphate pellets, containing about 15 milligrams of P, were placed in 200 grams of soil and stored for 2 weeks at four moisture tensions and three temperatures. Pellet residues were then removed and the amount of phosphorus remaining was determined. Small cores containing pellet residues and the surrounding soil contacted by fertilizer solution were removed for determination of water-soluble and total inorganic P. Phosphate phases present at the granule sites and the surrounding soil were identified by their optical properties.The mean amount of phosphorus remaining at the granule sites was 20.2 per cent. Although both moisture tension and temperature significantly affected the quantity of phosphorus retained, no consistent trend was apparent. Residues remaining at the site of application were found to be mixtures of anhydrous and dihydrated dicalcium phosphate, with the latter predominating. Moisture tension and temperature did not greatly alter the proportion of the two phases.Periodic precipitates or Liesegang rings of dicalcium phosphate were formed in the soil surrounding monocalcium phosphate pellets. Dicalcium phosphate dihydrate was the predominant phase. The proportion of dihydrated to anhydrous dicalcium phosphate increased as the temperature decreased and as the moisture tension increased.Water-soluble P increased significantly with increased moisture tension and was significantly greater at 5 °C. than at either 16 or 27 °C. The mean of all treatments was 5.6 per cent. Increased amounts of dicalcium phosphate dihydrate in the surrounding soil seemed to be responsible for the increase in water solubility.Between 89.5 and 99.2 per cent of the added phosphorus was recovered in the water and acid extracts of soil cores containing about 1.4 cm.3 of soil.


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