Soil phosphorus tests I: What soil phosphorus pools and processes do they measure?

2013 ◽  
Vol 64 (5) ◽  
pp. 461 ◽  
Author(s):  
Philip W. Moody ◽  
Simon D. Speirs ◽  
Brendan J. Scott ◽  
Sean D. Mason

The phosphorus (P) status of 535 surface soils from all states of Australia was assessed using the following soil P tests: Colwell-P (0.5 m NaHCO3), Olsen-P (0.5 m NaHCO3), BSES-P (0.005 m H2SO4), and Mehlich 3-P (0.2 m CH3COOH + 0.25 m NH4NO3 + 0.015 m NH4F + 0.013 m HNO3 + 0.001 m EDTA). Results were correlated with soil P assays selected to estimate the following: soil solution P concentration (i.e. 0.01 m CaCl2 extractable P; Colwell-P/P buffer index); rate of P supply to the soil solution (i.e. P released to FeO-impregnated filter paper); sorbed P (i.e. Colwell-P); mineral P (i.e. fertiliser reaction products and/or soil P minerals estimated as BSES-P minus Colwell-P); the diffusive supply of P (i.e. P diffusing through a thin gel film, DGT-P); and P buffer capacity (i.e. single-point P buffer index corrected for Colwell-P, PBICol). Across all soils, Colwell-P and BSES-P were highly correlated with FeO-P (r = 0.76 and 0.58, respectively). Colwell-P was moderately correlated with mineral P (r = 0.24), but not solution P. Olsen-P and Mehlich-P were both highly correlated with FeO-P (r = 0.80 and 0.78, respectively) but, in contrast to Colwell-P and BSES-P, also showed moderate correlations with soil solution P (r = 0.29 and 0.34, respectively) and diffusive P supply (r = 0.31 and 0.49, respectively). Correlation coefficients with mineral P were r = 0.29 for Olsen-P and r = 0.17 for Mehlich-P. Soils were categorised according to their pH, clay activity ratio, content of mineral P and CaCO3 content, and the relationships between the empirical soil P tests examined for each soil category. Olsen-P and Colwell-P were correlated across all soil categories (r range 0.66–0.90), and a widely applicable linear equation was obtained for converting one soil test to the other. However, the correlations between other soil tests varied markedly between soil categories and it was not possible to develop such widely applicable conversion equations. Multiple step-up linear regressions were used to identify the key soil properties affecting soil solution P, P buffer capacity, and diffusive P supply, respectively. For all soil categories, solution P concentration (measured by CaCl2-P) increased as rate of P supply (measured as FeO-P) increased and P buffer capacity decreased. As an assay of sorbed P, Colwell-P alone did not significantly (P > 0.05) explain any of the variability in soil solution P, but when used in the index (Colwell-P/P buffer index), it was highly correlated (r = 0.74) with CaCl2-P. Soil P buffer capacity was dependent on different properties in different soil categories, with 45–65% of the variation in PBI accounted for by various combinations of Mehlich-Al, Mehlich-Fe, total organic C, clay content, clay activity ratio, and CaCO3 content, depending on soil category. The diffusive supply of P was primarily determined by rate of P supply (measured as FeO-P; r range 0.34–0.49), with significant (P < 0.05) small improvements due to the inclusion of PBICol and/or clay content, depending on soil category. For these surface soil samples, key properties of pH, clay activity ratio, clay content, and P buffer capacity varied so widely within individual Australian Soil Orders that soil classification was not useful for inferring intrinsic surface soil P properties such as P buffer capacity or the relationships between soil P tests.

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.


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.


2010 ◽  
Vol 90 (2) ◽  
pp. 257-266 ◽  
Author(s):  
M M Arcand ◽  
D H Lynch ◽  
R P Voroney ◽  
P. van Straaten

Low soil test phosphorus (P) concentrations are common in organically managed soils in Canada. This field study examined the effect of residues from a buckwheat (Fagopyrum esculentum) green manure (GM) crop grown with an igneous and a sedimentary source of phosphate rock (PR) on in situ soil P supply, Olsen P, and soil microbial biomass P on an organic farm in Ontario, Canada. Phosphate rock application did not increase GM dry matter production, but did increase above-ground tissue P concentration with applications of the sedimentary PR (Calphos). In the following spring, in situ soil P supply and Olsen P were increased in GM residue-applied soils and in soils containing the Calphos PR, while microbial biomass P was largely unaffected. Release of P was detected when GM P concentration was greater than 2.9 g P kg-1. The results suggest the quality of the GM residues had more influence on P availability than the quantity applied to the soil; however, the low changes in available P (P supply and Olsen P) were not agronomically significant. Key words: Phosphate rock, soil phosphate supply, Olsen P, organic agriculture, green manure


Soil Research ◽  
2011 ◽  
Vol 49 (3) ◽  
pp. 247 ◽  
Author(s):  
P. W. Moody

Biologically available phosphorus (P) is divided operationally into two sources, dissolved reactive P (DRP) and bioavailable particulate P (BPP). Dilute CaCl2-extractable soil P (CaCl2-P) is considered to be the benchmark method for estimating DRP in soils, whereas P desorbed to iron-oxide impregnated filter paper (FeO-P) is the benchmark method for BPP in soils and sediments. Neither of these methods is in routine use in Australia. Selected soil P analyses were carried out on 31 diverse surface soils to develop relationships between the environmental benchmark methods and the routine soil P tests of Colwell-P, Olsen-P, and the single-point P buffer index (PBI). The index (Colwell-P/PBI) was highly correlated with CaCl2-P (r = 0.925, P < 0.001), and both Olsen-P and Colwell-P were highly correlated with FeO-P (r = 0.955 and 0.828, respectively; P < 0.001). It is suggested that these measures can be used as environmental risk indicators for soil P status. The critical values of these measures for optimum productivity were compared to the values of these measures corresponding to threshold values of currently used environmental risk indicators.


HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 864A-864
Author(s):  
B.R. Gardner ◽  
C.A. Sanchez

Lettuce is planted in the southwestern U.S. desert from September through December and harvested from November through April each year. During this period mean soil temperatures range from 7 to 30C. Lettuce produced on desert soils shows a large yield response to P. Soil solution P is replenished by desorption from the labile soil P fraction and this process is temperature sensitive. A field study was conducted over 6 years to evaluate the response of lettuce to soil solution P levels under different ambient soil temperature regimes. The soil temperatures under which lettuce was grown were varied each year by altering planting dates. Soil solution P levels were established and maintained each season using P sorption isotherm methodology. Lettuce responded to P in all experiments. Phosphorus levels required for maximum yield varied with each experiment. Soil P levels required for optimal yield were best correlated to mean soil temperatures during the last 20 days before harvest. Lettuce accumulates over 70% of its P during the heading stage of development and it is likely that during this period of rapid growth and nutrient uptake, solution P becomes limiting when soil temperatures are cool.


Soil Research ◽  
1995 ◽  
Vol 33 (6) ◽  
pp. 899 ◽  
Author(s):  
PW Moody ◽  
SA Yo ◽  
DG Edwards ◽  
LC Bell

A layer of Ca(H2PO4)2.H2O (MCP) or MCP plus CaSO4.2H2O was spread over duplicate columns of six soils to simulate the effects of banded MCP or superphosphate (MCP plus CaSO4.2H2O) on soil solution composition. A separate column was set up without fertilizer addition for each soil to act as a control (background) treatment. The soils used were 0-10 cm samples from two Kurosols, a Ferrosol, a Vertosol, a Kandosol, and a 50-60 cm sample from the Kandosol. Prior to fertilizer addition, the columns were wet up to the water content at a matric suction of 10 kPa. Following 5 days of fertilizer-soil contact, soil sections were recovered at 5 mm increments from the fertilizer layer to a distance of 50 mm. Soybean (Glycine max: (L.) Merr.) seedlings were grown for 48 h in each section and relative root elongation (RRE) was determined. Soil solution was then extracted from each section and analysed. The distance of phosphorus (P) movement from both MCP and MCP plus CaSO4.2H2O was better correlated with P buffer capacity determined at a solution P concentration of 3.2 �M than at 320 �M. This suggests that the precipitation reactions which occur at the fertilizer site when MCP dissolves are independent, of the soil, and it is only in soil sections further removed from the fertilizer source (i.e. with lower soil solution P concentrations) that the P sorption properties of the soil become important in determining the extent of P movement. The amount of inorganic P (Pi) in the soil solution was summed over all soil sections for each fertilizer source, and was correlated with citrate-dithionite extractable Fe and Al using step-up regression techniques. Citrate-dithionite extractable Fe was highly correlated with P-i (r = -0.937, P < 0.001), and the addition of citrate-dithionite extractable Al did not significantly (P = 0.05) increase the variation accounted for. RRE decreased in proximity to the fertilizer. When RRE was plotted against the electrical conductivity of the soil solution, all data points fell below the regression line previously obtained for various salts (Moody et al. Aust. J. Soil Res. 1995, 33, 673-87), indicating that the reduction in RRE was not due solely to osmotic effects. Multiple regression analysis indicated that a combination of the activities of Al3+ (aAl) and Mn2+ (aMn) explained 83% of the variation in RRE when both fertilizer sources were considered in all soils except the Kurosols. There was evidence of organic complexing of soil solution Al in the two Kurosols and so an accurate estimate of Al3+ activity could not be made. For the soils other than the Kurosols, separate regressions of RRE against ant and a(Mn) indicated a 10% reduction in RRE set activities of 1.9 and 70 �M, respectively. Based on these activities, banding of MCP and MCP plus CaSO4.2H2O caused Al toxicity in all soils, and Mn toxicity in all soils except one of the Kurosols. Manganese toxicity occurred further from the fertilizer band than Al toxicity in the Ferrosol and the Kandosol. The dual occurrence of Al and Mn toxicities indicates that both factors need to be considered simultaneously when determining the effects of banded fertilizer on RRE.


Author(s):  
Peter B. Tinker ◽  
Peter Nye

We noted in chapter 1 that the concentration of solute in the soil solution is buffered by solute adsorbed on the soil surfaces. We also show in chapter 4 that the overall mobility of ions is related to their amounts and mobilities in the solid and solution. In this chapter, we focus on the soil solution concentration, primarily to show how the factors controlling it can be incorporated in models of the growth of crops and the leaching of nutrients or pollutants, such as those described in chapters 10 and 11. We examine the general principles governing the interchange of solutes between all phases in the soil, dealing first with inorganic ions, especially plant nutrients and heavy metals; and later with organic solutes, including biocides, which may also occur in the vapour phase. We also consider the reactions between metal ions and other organic or inorganic ions in solution to form complexes, such as CuOH+. The method of displacing the pore solution from a column of soil with ethanol, introduced by Ischtscherikow (1907), has been examined by Moss (1963, 1969). He found, in accord with theory (section 3.1.3), that the activity ratios (K)/(Ca + Mg)1/2 and (K)/(Ca)1/2 determined in the displaced solutions remained constant over considerable changes in soil moisture level to the point of saturation. He also found that the activity ratio (K)/(Ca + Mg)1/2 in the extracts from a wide range of soils agreed well with the activity ratio determined by the null point method of Beckett & Craig (1964). In this method, the soil is shaken with dilute CaCl2 solution containing graded amounts of potassium, and the activity ratio at which the soil does not gain or lose potassium to the solution is determined. Ethanol appears to displace solution from the fine as well as the coarse pores, and successive fractions, devoid of alcohol, have the same composition. For small samples of soil, it is more convenient to add a heavy liquid that is immiscible with water, and extract the solution by centrifuging (Kinniburgh & Miles 1983). Suction methods are useful for following changes in composition of moist soils. They should be used with care since they change the pressure of CO2 and hence the concentration of the bicarbonate ion.


1992 ◽  
Vol 43 (1) ◽  
pp. 191 ◽  
Author(s):  
RL Aitken ◽  
PW Moody ◽  
BL Compton ◽  
EC Gallagher

Seedling macadamia (Macadamia integrifolia cv. Hinde) were grown in pots in two glasshouse experiments for 23 weeks. Experiment 1 comprised ten soils at two P levels (nil and a rate calculated to be non-limiting to growth) with six replications. Experiment 2 consisted of another two soils with eight rates of added P (0-2560 mg P per 4 L pot) and six replications. Whole plant tops were harvested, dried and weighed, and leaves analysed for P. In addition, leaves from Experiment 2 were analysed for Cu, Zn, Mn and Fe. Roots were recovered from the soils, separated into proteoid and non-proteoid root material, dried and weighed. Control (nil added P) soils were analysed for soil solution P and Colwell, Olsen, Bray 1 and 0.005 M CaCl2 extractable P. At 90% of maximum whole plant top growth, P concentration in the leaf was 0.08%. When the leaf Fe/P ratio < 0.07 in Experiment 2, there was a significant yield depression associated with symptoms of severe iron chlorosis. Critical soil P levels at 90% of maximum whole plant top growth were 50, 23 and 29 mg kg-1 for Colwell, Olsen and Bray 1 extractable P, respectively. It was not possible to define a critical CaCl2 extractable P or soil solution P concentration because of the large increase in relative growth with a small increase in these parameters. Proteoid root growth (as a percentage of total root weight) decreased with increasing level of soil phosphorus, and there were very few proteoid roots at >100 mg kg-1 Colwell extractable P. Applying P to maintain high soil test levels (>100 mg kg-1 Colwell extractable P) would have detrimental effects on proteoid root development.


2004 ◽  
Vol 39 (3) ◽  
pp. 241-246 ◽  
Author(s):  
Marcelo Eduardo Alves ◽  
Arquimedes Lavorenti

The remaining phosphorus (Prem) has been used for estimating the phosphorus buffer capacity (PBC) of soils of some Brazilian regions. Furthermore, the remaining phosphorus can also be used for estimating P, S and Zn soil critical levels determined with PBC-sensible extractants and for defining P and S levels to be used not only in P and S adsorption studies but also for the establishment of P and S response curves. The objective of this work was to evaluate the effects of soil clay content and clay mineralogy on Prem and its relationship with pH values measured in saturated NaF solution (pH NaF). Ammonium-oxalate-extractable aluminum exerts the major impacts on both Prem and pH NaF, which, in turn, are less dependent on soil clay content. Although Prem and pH NaF have consistent correlation, the former has a soil-PBC discriminatory capacity much greater than pH NaF.


2003 ◽  
Vol 83 (4) ◽  
pp. 395-403 ◽  
Author(s):  
Z. Zheng ◽  
L. E. Parent ◽  
J. A. MacLeod

The P dynamics in soils should be quantified in agricultural soils to improve fertilizer P (FP) efficiency while limiting the risk of P transfer from soils to water bodies. This study assessed P transformations following FP addition to Gleysolic soils. A pot experiment was conducted with five soils varying in texture from sandy loam to heavy clay, and receiving four FP rates under barley (Hordeum vulgare L.)-soybean (Glycine max L.) rotations. A modified Hedley procedure was used for soil P fractionation. Soil resin-P and NaHCO3-Pi contents were interactively affected by texture and FP. The NaHCO3-Po, NaOH-Po, HCl-P and H2SO4-P were only affected by soil texture. Proportions of 78 and 90% of the variation in labile and total P were, respectively, related to soil clay content. The FP addition increased resin-P, NaHCO3-Pi and NaOH-Pi and -Po contents in coarse-textured soils, but the amount added was not sufficient to mask the initial influence of soil texture on the sizes of soil P pools. Plant P uptake was proportional to FP rate but less closely linked to clay content. The average increase in labile P per unit of total FP added in excess of plant exports was 0.85, 0.8 2 , 0.73, 0.55 and 0.24 for the sandy loam, loam, clay loam, clay and heavy clay soil, respectively. The results of this study stress the important of considering soil texture in Gleysolic soils when assessing P accumulation and transformations in soils, due to commercial fertilizers applied in excess of crop removal. Key words: P fractions, clay content, fertilizer P, plant P uptake, soil texture


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