Dung decomposition in temperate dairy pastures. II. Contribution to plant-available soil phosphorus

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.

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.


2021 ◽  
Author(s):  
Zuzana Frkova ◽  
Chiara Pistocchi ◽  
Yuliya Vystavna ◽  
Katerina Capkova ◽  
Jiri Dolezal ◽  
...  

Abstract. At the early stages of pedogenesis, the dynamics of phosphorus (P) in soils are controlled by microbial communities, the physicochemical properties of the soil and the environmental conditions. While various microorganisms involved in carrying out biogeochemical processes have been identified, little is known about the actual contribution of microbial processes, such as organic P hydrolysis and microbial P turnover, to P cycling. We thus focused on processes driven by microbes and how they affect the size and cycling of organic and inorganic soil P pools along a soil chronosequence in the Chamser Kangri glacier forefield (Western Himalayas). The rapid retreat of the glacier allowed us to study the early stages of soil formation under cold arid climate. Biological P transformations were studied with the help of the isotopic composition of oxygen (O) in phosphate (δ18OP) coupled to sequential P fractionation performed on soil samples from four sites of different age spanning 0 to 100–150 years. The mineral P, i.e. 1M HCl-extractable P, represented still 95 % of the total P stock after approximately 100 years of soil development. Its isotopic composition was similar to the parent material also at the most developed site. Primary phosphate minerals, therefore, mostly composed this pool. The δ18OP of the available P and the P bound to Fe and Al oxides instead differed from that of the parent material, suggesting that these pools underwent biological turnover. The isotopic composition of O in of the available P was mostly controlled by the microbial P, suggesting fast exchanges occurred between these two pools possibly fostered by repeated freezing-thawing and drying-rewetting cycles. The release of P from organic P become increasingly important with soil age, constituting one third of the P flux to available P at the oldest site. Accordingly, the lighter isotopic composition of the P bound to Fe and Al oxides at the oldest site indicated that this pool contained phosphate released by organic P mineralization. Compared to previous studies on early pedogenesis under alpine or cold climate, our findings suggest a much slower decrease of the P-bearing primary minerals during the first 100 years of soil development under extreme condition. However, they provide evidence that, by driving short-term P dynamics, microbes play an important role in controlling the redistribution of primary P into inorganic and organic soil P pools.


SOIL ◽  
2022 ◽  
Vol 8 (1) ◽  
pp. 1-15
Author(s):  
Zuzana Frkova ◽  
Chiara Pistocchi ◽  
Yuliya Vystavna ◽  
Katerina Capkova ◽  
Jiri Dolezal ◽  
...  

Abstract. At the early stages of pedogenesis, the dynamics of phosphorus (P) in soils are controlled by microbial communities, the physicochemical properties of the soil and the environmental conditions. While various microorganisms involved in carrying out biogeochemical processes have been identified, little is known about the actual contribution of microbial processes, such as organic P hydrolysis and microbial P turnover, to P cycling. We thus focused on processes driven by microbes and how they affect the size and cycling of organic and inorganic soil P pools along a soil chronosequence in the Chamser Kangri glacier forefield (Western Himalayas). The rapid retreat of the glacier allowed us to study the early stages of soil formation under a cold arid climate. Biological P transformations were studied with the help of the isotopic composition of oxygen (O) in phosphate (δ18OP) coupled to sequential P fractionation performed on soil samples (0–5 cm depth) from four sites of different age spanning 0 to 100–150 years. The P bound to Ca, i.e., 1 M HCl-extractable P, still represented 95 % of the total P stock after approximately 100 years of soil development. Its isotopic composition was similar to the parent material at the most developed site. Primary phosphate minerals, possibly apatite, mostly comprised this pool. The δ18OP of the available P and the NaOH-extractable inorganic P instead differed from that of the parent material, suggesting that these pools underwent biological turnover. The δ18OP of the available P was mostly controlled by the microbial P, suggesting fast exchanges occurred between these two pools possibly fostered by repeated freezing–thawing and drying–rewetting cycles. The release of P from organic P becomes increasingly important with soil age, constituting one-third of the P flux to available P at the oldest site. Accordingly, the lighter isotopic composition of the P bound to Fe and Al oxides at the oldest site indicated that this pool contained phosphate released by organic P mineralization. Compared to previous studies on early pedogenesis under alpine or cold climate, our findings suggest a much slower decrease of the P-bearing primary minerals during the first 100 years of soil development under extreme conditions. However, they provide evidence that, by driving short-term P dynamics, microbes play an important role in controlling the redistribution of primary P into inorganic and organic soil P pools.


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.


2016 ◽  
Vol 3 (1) ◽  
pp. 17-24
Author(s):  
Shiferaw Boke ◽  
Sheleme Beyene ◽  
Heluf Gebrekidan

Data from 12 surface soils (0 – 15 cm depth)of three cropping systems (enset, maize and grazing land) and path analysis was used to evaluate effects of soil properties: pH, texture (Clay, silt and sand) , organic carbon (OC) cation exchange capacity (CEC),citrate-dithionite-bicarbonate (CDB) extractable Fe and Al (Fed and Ald) on total phosphorous (Pt), organic phosphorous (Po), Olsen P (Available P) and Chang and Jackson (1957) inorganic phosphorous (Pi) fractions. Correlation analysis was performed to study the relationships between soil properties and different soil P pools while path analysis model was used to evaluate direct and indirect effect of these soil properties on the P pools. Only soil properties that significantly contribute to the fit of the model were used. High significant values of coefficient of determination (R2) and low values of uncorrelated residual (U) values indicate the path analysis model explains most of the variations in soil Pt, Po, Olsen-P, Saloid-P, Ca-P, Al-P, and Fe-P pools. Soil pH had significantly high and positive direct effect (D = 0.618*) on Pt, (D = 1.044***) on saloid P, and (D = 1.109***) on Fe-P with modest and negative indirect effect (D= -0.478 and -0.405) on saloid P and Fe-P, respectively, through OC. The direct effect of clay on Ca-P, Al-P and Fe-P (readily available P forms) was significant and negative with a relatively higher indirect effect on Fe-P through pH suggesting that clay is dominant soil property that influences readily available P pools in Nitisols of the study area. Fed had significant and negative direct effect (D = -0.430*) on Olsen available P with low negative indirect effect ( D = -0.154) through pH results in significant and negative correlation (r = -0.657*). The significant and negative direct effect of Fed on Olsen P indicates that crystalline iron is the sink for available P. Relative influence of the soil properties on the soil P pools was in the order: pH > clay > Fed > OC.  These results show that most of P pools of Nitisols of Wolayita are best predicted from pH, clay (texture), Fed and OC. On the other hand, our data also show that the inclusion of other soil variables is needed to fully predict Ca-P and stable P pools.


2020 ◽  
Author(s):  
Curt A. McConnell ◽  
Jason P. Kaye ◽  
Armen R. Kemanian

Abstract. Soil phosphorus (P) management remains a critical challenge for agriculture worldwide, and yet we are still unable to predict soil P dynamics as confidently as that of carbon (C) or nitrogen (N). This is due to both the complexity of inorganic P (Pi) and organic P (Po) cycling and the methodological constraints that have limited our ability to trace P dynamics in the soil-plant system. In this review we describe the challenges to building parsimonious, accurate, and useful P models and to explore the potential of some new techniques to advance modeling efforts. To advance our understanding and modeling of P biogeochemistry, research efforts should focus on the following: 1) update the McGill and Cole (1981) model of Po mineralization by clarifying the role and prevalence of “biochemical” and “biological” Po mineralization which we hypothesize are not mutually exclusive and may co-occur along a continuum of Po substrate stoichiometry; 2) further understand the dynamics of phytate, a 6-C compound that can regulate the poorly understood stoichiometry of soil P; 3) explore the effects of C and Po saturation on P sorption and Po mineralization; and 4) resolve discrepancies between hypotheses about P cycling and the methods used to test these hypotheses.


1985 ◽  
Vol 65 (4) ◽  
pp. 651-665 ◽  
Author(s):  
T. L. ROBERTS ◽  
J. W. B. STEWART ◽  
J. R. BETTANY

A sequential extraction procedure was used to determine phosphorus fractions (resin, bicarbonate, hydroxide, sonicated hydroxide, acid and acid-peroxide digest with separate organic and inorganic P determinations) in surface and subsurface horizons taken from the upper, mid- and lower slope positions of four catenas (representing Brown, Dark Brown and Black Chernozemic soils, and a Luvisolic soil) which encompass a narrow environmental gradient of climate (annual precipitation: 300–475 mm) and vegetation. Trends in the local distribution of organic and inorganic soil P between upper and lower slope positions in any one catena were similar to the regional distribution patterns across all soil zones. Concentration of organic P, in both the surface and subsurface horizons, increased from the upper to the lower slope positions and from the Brown to the Black soils, while inorganic P decreased. The largest single organic fraction (hydroxide extractable) accounted for up to 22 and 17% of the total P (surface and subsurface horizons, respectively). Acid extractable P dominated the inorganic fractions, accounting for 40–63% of the total P (surface and subsurface horizons, respectively). The distribution of organic P along the catenas and among the soil zones was related to the transformations of inorganic P caused by differences in weathering intensity between slope positions and across the Province. Key words: Catena, climo-toposequence, sequential P extraction


1990 ◽  
Vol 114 (1) ◽  
pp. 1-9 ◽  
Author(s):  
L. M. Condron ◽  
K. M. Goh

SUMMARYThe nature and availability of phosphorus in long-term fertilized pasture soils was investigated in a series of field trials, which included liming, N fertilizer and cultivation and involved monitoring plant P uptake and changes in topsoil (0–7·5 cm) P fractions for 2 years (1982–83). Liming increased soil organic P mineralization. This was indicated by significant decreases in extractable organic P and concomitant increases in microbial biomass P in the limed soils, although these changes in soil P had no significant effect on pasture yield and P uptake. On the other hand, N fertilizer increased pasture yield and P uptake but had little effect on the amounts of P in the different soil P fractions. In the cultivated soils, increases in plant-available inorganic P were attributed to the release of P during decomposition of plant residues, while the maintenance of fallow conditions decreased amounts of microbial P in these soils.


Agronomy ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1483
Author(s):  
Thanh Tung Nguyen ◽  
Yuka Sasaki ◽  
Mitsuhiko Katahira ◽  
Dhirendranath Singh

Cow manure is a good source of phosphorus (P). Here, we investigated whether the amount of P fertilizer can be reduced when cow manure is applied to paddy soil based on growth, P uptake, yield, and soil P status evaluation. Treatments included unfertilized control (CK); manure plus chemical nitrogen (N), potassium (K), and P fertilizer (MNK P); MNK and 75% P (MNK ¾ P); MNK and 50% P (MNK ½ P); MNK and 25% P (MNK ¼ P); and MNK. Manure was applied at the rate of 10 t ha−1 in fresh weight base. The P fertilizer was applied at 34.9 kg P ha−1 as full dose. Treatment with MNK resulted in the same growth, P uptake, and yield as that with the P fertilizer. P uptake and yield did not respond to P input from chemical fertilizer owing to high soil Olsen P levels. Moreover, MNK could maintain soil Olsen P and total P. Manure application resulted in a positive partial P balance. These results suggest that manure application can cut P fertilizer requirements in P-rich soils, while maintaining soil P for optimal rice growth and yield. By using cow manure in rice production, farmers can conserve finite P resources.


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