A comparison of some surface soil phosphorus tests that could be used to assess P export potential

Soil Research ◽  
2007 ◽  
Vol 45 (5) ◽  
pp. 397 ◽  
Author(s):  
David Nash ◽  
Murray Hannah ◽  
Kirsten Barlow ◽  
Fiona Robertson ◽  
Nicole Mathers ◽  
...  

Phosphorus (P) exports from agricultural land are a problem world-wide and soil tests are often used to identify high risk areas. A recent study investigated changes in soil (0–20 mm), soil water and overland flow in 4 recently laser-graded (<1 year) and 4 established (laser-graded >10 years) irrigated pastures in south-eastern Australia before and after 3 years of irrigated dairy production. We use the results from that study to briefly examine the relationships between a series of ‘agronomic’ (Olsen P, Colwell P), environmental (water-extractable P, calcium chloride extractable P, P sorption saturation, and P sorption), and other (total P, organic P) soil P tests. Of the 2 ‘agronomic’ soil P tests, Colwell P explained 91% of the variation in Olsen P, and Colwell P was better correlated with the other soil tests. With the exception of P sorption, all soil P tests explained 57% or more of the total variation in Colwell P, while they explained 61% or less of Olsen P possibly due to the importance of organic P in this soil. Variations in total P were best explained by the organic P (85%), Calcium chloride extractable P (83%), water-extractable P (78%), and P sorption saturation (76%). None of the tests adequately predicted the variation in P sorption at 5 mg P/L equilibrating solution concentration. The results of this limited study highlight the variability between soil P tests that may be used to estimate P loss potential. Moreover, these results suggest that empirical relationships between specific soil P tests and P export potential will have limited resolution where different soil tests are used, as the errors in the relationship between soil test P and P loss potential are compounded by between test variation. We conclude that broader study is needed to determine the relationships between soil P tests for Australian soils, and based on that study a standard protocol for assessing the potential for P loss should be developed.

Soil Research ◽  
2004 ◽  
Vol 42 (1) ◽  
pp. 115 ◽  
Author(s):  
S. R. Aarons ◽  
H. M. Hosseini ◽  
L. Dorling ◽  
C. J. P. Gourley

Changes in dung and soil inorganic and organic P pools were measured in an experiment investigating the effects of dung on soil properties in 2 grazed dairy pasture systems (low and high input). Total dung P and bicarbonate-extractable P pools were measured in decomposing pads and compared with the changes in inorganic and organic bicarbonate-extractable soil P, P sorption, and microbial P flush of soils beneath dung pads and control 'pads' where nothing was applied. Bicarbonate-extractable total P in the dung pads declined to the same level in both systems by the last sample date. Organic P comprised a similar proportion (36%) of the bicarbonate-extractable total P pool in dung from both low and high input systems. However, the transformations of dung P were different in each system, with the bicarbonate-extractable total P in the low input dung increasing by 25% before declining, and a greater decrease in percentage bicarbonate-extractable organic P in this system.Bicarbonate-extractable soil organic P did not vary under dung pads despite the large increases in Olsen and Colwell P observed. Soil Olsen P trends observed in the low and high input systems indicate a potential for leaching losses of P in high input systems compared with low. This increase in soil Olsen P was not due to decreased P sorption as dung did not reduce the sorption capacity of the soil. Microbial soil P increased under dung pads only after 60 days in this experiment. Neither the organic P nor microbial P pools contributed significantly to soil labile P pools in these temperate dairy pasture systems. The transformations of P thought to occur during the decomposition of dung are discussed.


2016 ◽  
Vol 73 (12) ◽  
pp. 2953-2958 ◽  
Author(s):  
H. E. Andersen ◽  
J. Windolf ◽  
B. Kronvang

Abstract We investigated leaching of dissolved phosphorus (P) from 45 tile-drains representing animal husbandry farms in all regions of Denmark. Leaching of P via tile-drains exhibits a high degree of spatial heterogeneity with a low concentration in the majority of tile-drains and few tile-drains (15% in our investigation) having high to very high concentration of dissolved P. The share of dissolved organic P (DOP) was high (up to 96%). Leaching of DOP has hitherto been a somewhat overlooked P loss pathway in Danish soils and the mechanisms of mobilization and transport of DOP needs more investigation. We found a high correlation between Olsen-P and water extractable P. Water extractable P is regarded as an indicator of risk of loss of dissolved P. Our findings indicate that Olsen-P, which is measured routinely in Danish agricultural soils, may be a useful proxy for the P leaching potential of soils. However, we found no straight-forward correlation between leaching potential of the top soil layer (expressed as either degree of P saturation, Olsen-P or water extractable P) and the measured concentration of dissolved P in the tile-drain. This underlines that not only the source of P but also the P loss pathway must be taken into account when evaluating the risk of P loss.


Soil Research ◽  
2020 ◽  
Vol 58 (2) ◽  
pp. 117 ◽  
Author(s):  
Musibau O. Azeez ◽  
Gitte Holton Rubæk ◽  
Ingeborg Frøsig Pedersen ◽  
Bent T. Christensen

Soil phosphorus (P) reserves, built up over decades of intensive agriculture, may account for most of the crop P uptake, provided adequate supply of other plant nutrients. Whether crops grown on soils with reduced supply of other nutrients obtain similar use-efficiency of soil P reserves remains unclear. In treatments of the Askov Long-Term Experiment (initiated in 1894 on light sandy loam), we quantified changes in soil total P and in plant-available P (Olsen P, water extractable P and P offtake in wheat grains) when P-depleted soil started receiving P in rock phosphate and when P application to soil with moderate P levels ceased during 1997–2017. Additionally we studied treatments with soil kept unfertilised for &gt;100 years and with soil first being P depleted and then exposed to surplus dressings of P, nitrogen (N) and potassium in cattle manure. For soil kept unfertilised for &gt;100 years, average grain P offtake was 6 kg ha–1 and Olsen P averaged 4.6 mg kg–1, representing the lower asymptotic level of plant-available P. Adding igneous rock phosphate to severely P-depleted soil with no N fertilisation had little effect on Olsen P, water extractable P (Pw), grain yields and P offtake. For soils with moderate levels of available P, withholding P application for 20 years reduced contents of Olsen P by 56% (from 16 to 7 mg P kg–1) and of Pw by 63% (from 4.5 to 1.7 mg P kg–1). However, the level of plant-available P was still above that of unfertilised soil. Application of animal manure to P-depleted soil gradually raised soil P availability, grain yield and P offtake, but it took 20 years to restore levels of plant-available P. Our study suggests symmetry between rates of depletion and accumulation of plant-available P in soil.


2018 ◽  
Vol 64 (No. 9) ◽  
pp. 441-447 ◽  
Author(s):  
Jarosch Klaus A ◽  
Santner Jakob ◽  
Parvage Mohammed Masud ◽  
Gerzabek Martin Hubert ◽  
Zehetner Franz ◽  
...  

Soil phosphorus (P) availability was assessed with four different soil P tests on seven soils of the Ultuna long-term field experiment (Sweden). These four soil P tests were (1) P-H<sub>2</sub>O (water extractable P); (2) P-H<sub>2</sub>O<sub>C10</sub> (water extractable P upon 10 consecutive extractions); (3) P-AL (ammonium lactate extractable P) and (4) P-C<sub>DGT</sub> (P desorbable using diffusive gradients in thin films). The suitability of these soil P tests to predict P availability was assessed by correlation with plant P uptake (mean of preceding 11 years) and soil P balancing (input vs. output on plot level for a period of 54 years). The ability to predict these parameters was in the order P-H<sub>2</sub>O<sub>C10</sub> &gt; P-C<sub>DGT</sub> &gt; P-H<sub>2</sub>O &gt; P-AL. Thus, methods considering the P-resupply from the soil solid phase to soil solution performed clearly better than equilibrium-based extractions. Our findings suggest that the P-AL test, commonly used for P-fertilizer recommendations in Sweden, could not predict plant P uptake and the soil P balance in a satisfying way in the analysed soils.


Soil Research ◽  
1997 ◽  
Vol 35 (2) ◽  
pp. 327 ◽  
Author(s):  
R. C. Dalal

Vertisols originally carrying brigalow vegetation (Acacia harpophylla F. Muell. ex Benth.) and cultivated for cereal cropping for up to 45 years were examined for trends in available phosphorus (P) [sodium bicarbonate extractable P (bicarb. P) and dilute acid extractable P (acid P)], organic P, inorganic P, and total P. The soils (0-0 · 1 m depth) in their virgin state contained 60 mg/kg of bicarb. P, 168 mg/kg of acid P, 239 mg/kg of organic P, and 330 mg/kg of inorganic P. All fractions of soil P declined following first-order decay with the period of cereal cropping; the rates of bicarb. P and acid P (available P) decline were 0 · 047 and 0 · 08/year. The organic P, inorganic P, and total P declined more slowly than available P; the respective rates were 0 · 026, 0 · 019, and 0 · 021/year. The rates of loss of total P and inorganic P were much higher from the clay-size fraction than the silt-size or sand-size fraction, with the t½ value of inorganic P in the sand-size fraction being almost 20 times greater than any other fraction. On the other hand, organic P loss from the clay-size fraction was much less; presumably, clay provides physical protection to soil organic matter and hence to organic P from decomposition. On average, bicarb. P and acid P declined at the rate of 1 · 3±0 · 3 and 4 · 6±1 · 4 mg P/kg soil · year. The declines in organic P and inorganic P were 3 · 0±0.4 and 4 · 1±1 · 2 mg P/kg soil · year, with a loss in total P of 7 · 2±1 · 3 mg P/kg soil · year. There was no significant shift in the ratio organic P: total P (38±7%) with the period of cultivation and cereal cropping. Organic P was closely correlated with organic C and total N in these soils. The mean amounts of P contained in the grain and the dry matter of each cereal crop from 1981 and 1984 were 7 · 6±1 · 8 and 8 · 3±2 · 4 kg P/ha, respectively. Thus, most of the soil total P loss could be accounted for by crop removal, of which organic P contributed about 40%. However, the continuous decline in available P, especially below 15 mg P/kg soil, warrants remedial measures to arrest the decline in the yields of crops grown on these Vertisols.


Soil Research ◽  
2001 ◽  
Vol 39 (4) ◽  
pp. 759 ◽  
Author(s):  
L. L. Burkitt ◽  
C. J. P. Gourley ◽  
P. W. G. Sale ◽  
N. C. Uren ◽  
M. C. Hannah

Nine pasture soils from high rainfall zones of southern Victoria were analysed for a range of chemical and physical properties before receiving a single application of P fertiliser in the form of triple superphosphate (TSP), single superphosphate (SSP), or TSP and lime (5 t/ha) at amounts ranging from 0 to 280 kg P/ha. Soils were analysed for bicarbonate-extractable P concentration, using both the Olsen P and Colwell P methods, 6 and 12 months after fertiliser application. A strong positive linear relationship existed at all sites between the amount of P applied and both the Olsen P and Colwell P concentrations. The slopes of these relationships measured the change in extractable P concentration (Δ EP) per unit of P applied, whilst the inverse of the ΔEP value indicated the amount of P fertiliser required above maintenance to increase the extractable P concentration by 1 mg/kg. These values ranged from 5 to 15 kg P/ha, depending on soil type. The ΔEP measured by the Olsen (Δ EP Olsen ) method was closely related to selected soil properties and P sorption measures, whilst the ΔEPColwell values were also closely related to selected soil properties and P sorption measures, but only when one particular site, an acidic sand, with a high organic carbon content was excluded from the analysis. In general, simple, direct measures of soil P sorption could allow the estimation of ΔEP values on different soil types. The application of P in the form of SSP resulted in a trend for higher ΔEP values than occurred with TSP. This difference was significant on 3 sites (P < 0.05), but depended on the method of extraction and the time after fertiliser application. The application of lime significantly (P < 0.001) increased soil pH (H2 O and CaCl 2 ) and decreased the concentration of exchangeable Al, 6 months after treatments were applied, but generally had little impact on ΔEP values.


2011 ◽  
Vol 60 (2) ◽  
pp. 343-358
Author(s):  
Péter Csathó ◽  
Marianna Magyar ◽  
Erzsébet Osztoics ◽  
Katalin Debreczeni ◽  
Katalin Sárdi

A szabadföldi trágyázási (tartam)kísérletek eredményeit talaj-, illetve diagnosztikai célú növényvizsgálatok segítségével tudjuk kiterjeszteni, általánosítani – figyelembe véve természetesen a kiterjesztés korlátait is. Célszerűnek láttuk ezen túl a talaj könnyen oldható tápelem-, közöttük P-tartalmát is meghatározni a hazánkban hivatalosan elfogadott AL- (ammónium-laktátos) módszer mellett az Európai Unióban és Észak-Amerikában alkalmazott P-tesztekkel is (CaCl2-, H2O-, Olsen-, Bray1-, LE-, Mehlich3- stb.) a hazai OMTK kísérletek talajmintáiban. A kísérleti helyek talajtulajdonságaiban megnyilvánuló jelentős különbségek lehetőséget adnak rá, hogy a talaj P-teszteket – és a növényi P-felvételt – jellegzetes hazai talajokon, sokszor szélsőséges talajparaméterek mellett vizsgáljuk. Az egyes P-szintek között a 28 év átlagában mintegy évi 50 kg P2O5·ha-1volt a különbség. A P0-szinten mért P-tartalmak jól jelezték az egyes kísérleti helyek talajának eltérő P-ellátottságát, illetve, közvetve, fizikai féleségében, pH és mészállapotában meglévő különbségeket. A P2-szinten – a hazai talajokra, P-igényes növényekre a hazai szabadföldi P-trágyázási tartamkísérleti adatbázisban talált összefüggésekre alapozott – új AL-P határértékek szerint csupán a bicsérdi csernozjom barna erdőtalajon nem javult a P-ellátottság legalább a „jó” szintig. Vizsgálataink megerősítették az AL-módszer függőségét a CaCO3-tartalomtól: a Mehlich3 módszerrel való összefüggésben a karbonátmentes és a karbonátos talajok csoportja erőteljesen elkülönült egymástól. Az AL-P korrekció elvégzése, azaz az AL-P értékeknek egy standard talajtulajdonság-sorra való konvertálása (KA: 36; pH(KCl): 6,8; CaCO3: 0,1%) látványosan csökkentette az AL-módszernek a talaj CaCO3-tartalmától való függőségét. Az AL-P és Olsen-P, valamint a korrigált AL-P és Olsen-P tartalmak összehasonlításában ugynakkor ugyanez az összefüggés nem volt állapítható, ami arra utal, hogy az Olsen módszer bizonyos fokig szintén pH- és mészállapot függő. Kísérleti eredményeink megerősítették a Sarkadi-féle AL-P korrekciós modell helytálló voltát. Fenti megállapításunkat ugyanakkor a növényi P-tartalmakkal való összefüggéseknek is igazolniuk kell. Szükséges tehát a talajvizsgálati eredményeknek a diagnosztikai célú növényvizsgálatokkal, valamint a terméseredményekkel való összevetése. A tartamkísérletek talajai lehetőséget nyújtanak a környezetvédelmi célú P-vizsgálatok értékelésére, a talaj P-feltöltöttsége környezeti kockázatának becslésére. Ezekkel a kérdésekkel a cikksorozat további részeiben kívánunk foglalkozni.


2013 ◽  
Vol 59 (No. 11) ◽  
pp. 530-536 ◽  
Author(s):  
S. Wang ◽  
X. Liang ◽  
G. Liu ◽  
H. Li ◽  
X. Liu ◽  
...  

The effects of phosphorus (P) fertilizer on P loss potential, soil Olsen-P and neutral phosphatase activities in paddy soils fertilized with superphosphate or pig manure (PM) were evaluated in this paper. Data were collected from a field experiment in the Tai Lake Basin, China. Superphosphate rates were 0, 17.5, 26.7, and 35.0 kg P/ha, and PM rates were 0, 1.4, 2.1, and 2.8 t/ha for each crop, respectively. Soil Olsen-P in the plow layer increased to a greater extent with PM than with superphosphate. Pig manure increased neutral phosphatase activities in the plow layer compared with PM-free treatment. In contrast, superphosphate inhibited neutral phosphatase activities compared with superphosphate-free treatment. Spring application of P fertilizer markedly increased the total P of surface water in November (&lt; 0.01 vs. 0.10 mg/L) compared with P-free treatment. The total P of shallow groundwater at a 75 cm depth was ~0.01 mg/L. Phosphorus fertilizer did not influence Olsen-P or neutral phosphatase activities under the plow layer. Downward movement of P did not occur. Appropriate rate of P application of 26.2 kg P/ha for each crop in this soil reduced the risk of P loss in the paddy wetland ecosystem.


2003 ◽  
Vol 83 (4) ◽  
pp. 337-342 ◽  
Author(s):  
A. Liu ◽  
C. Hamel ◽  
S. H. Begna ◽  
B. L. Ma ◽  
D. L. Smith

The ability of arbuscular mycorrhizal (AM) fungi to help their host plant absorb soil P is well known, but little attention has been paid to the effect of AM fungi on soil P depletion capacity. A greenhouse experiment was conducted to assess, under different P levels, the effects of mycorrhizae on extractable soil P and P uptake by maize hybrids with contrasting phenotypes. The experiment had three factors, including two mycorrhizal treatments (mycorrhizal and non-mycorrhizal), three P fertilizer rates (0, 40, and 80 mg kg-1) and three maize hybrids [leafy normal stature (LNS), leafy reduced stature (LRS) and a conventional hybrid, Pioneer 3979 (P3979)]. Extractable soil P was determined after 3, 6 and 9 wk of maize growth. Plant biomass, P concentration and total P content were also determined after 9 wk of growth. Fertilization increased soil extractable P, plant biomass, P concentration in plants and total P uptake. In contrast to P3979, the LNS and LRS hybrids had higher biomass and total P content when mycorrhizal. Mycorrhizae had less influence on soil extractable P than on total P uptake by plants. The absence of P fertilization increased the importance of AM fungi for P uptake, which markedly reduced soil extractable P under AM plants during growth. This effect was strongest for LNS, the most mycorrhizae-dependent hybrid, intermediate for LRS, and not significant for the commercial hybrid P3979, which did not respond to AM inoculation. Key words: Arbuscular mycorrhizal fungi, extraradical hyphae, maize hybrid,plant biomass, P uptake, soil extractable P


2018 ◽  
Vol 25 (6) ◽  
pp. 1736-1744 ◽  
Author(s):  
Jörg Prietzel ◽  
Wantana Klysubun

Phosphorus (P) K-edge X-ray absorption near-edge structure (XANES) spectra of orthophosphate (oPO4) bound to soil FeIII minerals (e.g. ferrihydrite, goethite) show a pre-edge signal at 2148–2152 eV. It is unknown whether organic P bound to FeIII oxyhydroxides also show this feature. Otherwise, Fe-bound soil P may be underestimated by P K-edge XANES spectroscopy, because a large portion of Fe oxyhydroxide-bound P in soils is organic P. K-edge XANES spectra were obtained for different organic P compounds present in soils [inositol hexaphosphate (IHP), glucose-6-phosphate (G6P), adenosine triphosphate (ATP)] after sorption to ferrihydrite or goethite and compared with spectra of oPO4 adsorbed to these minerals. P sorption to ferrihydrite increased in the sequence IHP ≪ G6P < oPO4 < ATP. P sorption to goethite increased in the sequence G6P < oPO4 ≪ ATP = IHP. Pre-edge signals in P K-edge XANES spectra of organic P adsorbed to Fe oxyhydroxides were markedly smaller compared with those of oPO4 adsorbed to these minerals and absent for FeIII oxyhydroxide-bound ATP as well as goethite-bound IHP. Linear combination fitting (LCF) performed on spectra of IHP, G6P or ATP adsorbed to ferrihydrite or goethite, using only spectra of FeIII oxyhydroxide-bound oPO4 as reference compounds for Fe-bound P, erroneously assigned >93% (ferrihydrite) or >41% (goethite) of Fe-bound P to non-Fe-bound P species. Inclusion of FeIII oxyhydroxide-bound IHP as reference compounds markedly increased the recovery of oxyhydroxide-bound organic P. Thus, Fe-bound soil P has probably often been underestimated by LCF in soil XANES studies where IHP adsorbed to ferrihydrite and to goethite were not included as reference compounds.


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