Estimation of the phosphorus sorption capacity of acidic soils in Ireland

The test for the degree of phosphorus (P) saturation (DPS) of soils is used in northwest Europe to estimate the potential of P loss from soil to water. It expresses the historic sorption of P by soil as a percentage of the soil's P sorption capacity (PSC), which is taken to be α (Al_ox + Fe_ox), where Al_ox and Fe_ox are the amounts of aluminium and iron extracted by a single extraction of oxalate. All quantities are measured as mmol kg soil^?1, and a value of 0.5 is commonly used for the scaling factor α in this equation. Historic or previously sorbed P is taken to be the quantity of P extracted by oxalate (P_ox) so that DPS = P_ox/PSC. The relation between PSC and Al_ox, Fe_ox and P_ox was determined for 37 soil samples from Northern Ireland with relatively large clay and organic matter contents. Sorption of P, measured over 252 days, was strongly correlated with the amounts of Al_ox and Fe_ox extracted, but there was also a negative correlation with P_ox. When PSC was calculated as the sum of the measured sorption after 252 days and P_ox, the multiple regression of PSC on Al_ox and Fe_ox gave the equation PSC = 36.6 + 0.61 Al_ox+ 0.31 Fe_ox with a coefficient of determination (R²) of 0.92. The regression intercept of 36.6 was significantly greater than zero. The 95% confidence limits for the regression coefficients of Al_ox and Fe_ox did not overlap, indicating a significantly larger regression coefficient of P sorption on Al_ox than on Fe_ox. When loss on ignition was employed as an additional variable in the multiple regression of PSC on Al_ox and Fe_ox, it was positively correlated with PSC. Although the regression coefficient for loss on ignition was statistically significant (P < 0.001), the impact of this variable was small as its inclusion in the multiple regression increased R² by only 0.028. Values of P sorption measured over 252 days were on average 2.75 (range 2.0–3.8) times greater than an overnight index of P sorption. Measures of DPS were less well correlated with water‐soluble P than either the Olsen or Morgan tests for P in soil.     

Effect of triple superphosphate and biowaste compost on mycorrhizal colonization and enzymatic P mobilization under maize in a long‐term field experiment

Phosphorus (P) fertilizers and mycorrhiza formation can both significantly improve the P supply of plants, but P fertilizers might inhibit mycorrhiza formation and change the microbial P cycling. To test the dimension and consequences of P fertilizer impacts under maize (Zea mays L.), three fertilizer treatments (1) triple superphosphate (TSP, 21–30 kg P ha^?1 annually), biowaste compost (ORG, 30 Mg ha^?1 wet weight every third year) and a combination of both (OMI) were compared to a non‐P‐fertilized control (C) in 2015 and 2016. The test site was a long‐term field experiment on a Stagnic Cambisol in Rostock (NE Germany). Soil microbial biomass P (P_mic) and soil enzyme activities involved in P mobilization (phosphatases and ß‐glucosidase), plant‐available P content (double lactate‐extract; P_DL), mycorrhizal colonization, shoot biomass, and shoot P concentrations were determined. P deficiency led to decreased P immobilization in microbial biomass, but the maize growth was not affected. TSP application alone promoted the P uptake by the microbial biomass but reduced the mycorrhizal colonization of maize compared to the control by more than one third. Biowaste compost increased soil enzyme activities in the P cycling, increased P_mic and slightly decreased the mycorrhizal colonization of maize. Addition of TSP to biowaste compost increased the content of P_DL in soil to the level of optimal plant supply. Single TSP supply decreased the ratio of P_DL:P_mic to 1:1 from about 4:1 in the control. Decreased plant‐benefits from mycorrhizal symbiosis were assumed from decreased mycorrhizal colonization of maize with TSP supply. The undesirable side effects of TSP supply on the microbial P cycling can be alleviated by the use of compost. Thus, it can be concluded that the plant‐availability of P from soil amendments is controlled by the amendment‐specific microbial P cycling and, likely, P transfer to plants.     

Genetic Variations of Brassica Cultivars for P Acquisition in a P Stress Environment and Comparison of P Sources for Sustainable Crop Management

To compare the growth performance of Brassica in a phosphorus (P) stress environment and response to added P, six Brassica cultivars were grown in pots for 49 days after sowing, using a soil low in P [sodium bicarbonate (NaHCO₃)–extractable P = 3.97 mg kg^?1, Mehlich III–extractable P = 6.13 mg kg^?1] with (+P = 60 mg P kg^?1 soil) or without P addition (0P). Phosphorus‐stress markedly reduced biomass accumulation and P uptake by roots and shoots. However, root–shoot ratio remained unaffected, implying that relative partitioning of biomass into roots and shoots had little role to play in shoot dry matter (SDM) production by cultivars. Biomass correlated significantly (P < 0.01) with total P uptake. Under P stress, the cultivars that produced greater root biomass were able to accumulate more total P content (r = 0.95^**), which in turn was related positively to SDM and total biomass (r > 0.89^**) and negatively to P‐stress factor (r = ?0.91^**). There was no correlation between P efficiency (PE) (relative shoot growth) and plant P, but PE showed a very significant correlation with shoot P content and SDM. Wide differences in growth and better performance of cultivars such as ‘Brown Raya’ and ‘Con‐1’ under P stress encouraged screening of more germplasm, especially in the field, to identify P‐tolerant cultivars.

In another study, potential relative agronomic effectiveness (RAE) of sparingly soluble P sources was investigated by growing two contrasting cultivars. The P sources incorporated into soil at 0, 10, 25, 50, and 100 mg P Kg^?1 were (i) powdered Jordan rock P (RP), (ii) triple superphosphate (TSP), (iii) powdered low‐grade TSP [TSP(PLG)], (iv) a mixture of RP + TSP compacted into pellets at 50:50 P ratio [RP + TSP(PelC)], and (v) a mixture of powdered RP + TSP at 50:50 P ratio [RP + TSP(PM)]. The RP was low in RAE and only 5 and 29% as effective as TSP in producing dry matter (DM) of P‐sensitive ‘B.S.A.’ and P‐tolerant ‘Brown Raya’ cultivars, respectively. There were no significant differences between TSP and RP + TSP(PelC) in DM yield of ‘Brown Raya,’ whereas, in the case of ‘B.S.A.’ RP + TSP(PM) was significantly less effective than RP + TSP(PelC) compared with TSP. Combined utilization of superior genome and P sources [such as TSP(PLG) and RP + TSP(PelC)] produced from low‐grade RP (that cannot be used either for direct application or acidulated P fertilizers) can be used as an alternative strategy for sustainable crop production, especially in resource‐poor environments. Further field trials at the level of cropping systems are needed.     

Phosphorus characterization of manure composts and combined organic fertilizers by a sequential‐fractionation method

Characterization of the forms of phosphorus (P) in organic soil amendments was conducted by sequential P fractionation. More than 60% of total P was inorganic P (P_i). The major P_i forms in the cattle‐manure composts were NaHCO₃‐ and HCl‐extractable P fractions. HCl‐extractable P_i was the predominant P form and a considerable proportion of the total P was present in the HCl‐extractable organic P fraction in the poultry manure composts and combined organic fertilizers.     

Short‐term effects of application of different rates of inorganic P and residue P on soil P pools and wheat growth

Phosphorus (P) can be added to soil as inorganic P or crop‐residue P, but little is known about how these two forms of P addition affect soil P pools and how their effect changes with the rate of P addition. A glasshouse experiment was conducted to assess the effect of inorganic P and P added as residues at different rates on (1) soil P pools at two time points: immediately after amendment and 42 d later, and (2) growth and P uptake by wheat at flowering (day 42). Three types of legume residues (faba bean young shoot, chickpea mature shoots with pods, and white lupin mature shoots without pods) were added to a loamy‐sand soil at a rate of 5 or 15 g residue kg^–1. Inorganic P was added at four different rates (3, 10, 30, and 100 mg P kg^–1) to give P‐addition rates corresponding to the total P added with the different residues at the two residue rates. Soil P pool concentrations (microbial P, resin‐P, NaHCO₃‐P, NaOH‐P, HCl‐P, and residual P) and wheat growth and P uptake (shoot and root) were measured after 6 weeks. Compared to inorganic P addition, P added with residues led to a 10%–80% greater increase in shoot biomass at the two highest P‐addition rates. Wheat P uptake was positively correlated with resin‐P and microbial‐P concentrations in residue‐P‐amended soil, but with resin‐P and NaOH‐P_i concentrations in soil amended with inorganic P. The concentration of HCl‐P decreased by up to 30% from day 0 to day 42 in the residue treatments and that of residual P decreased by about 20% in all treatments during this period suggesting that these nonlabile P pools are quite dynamic and could serve as P source for plants.     

EDTA extractable phosphorus in soils as related to available and inorganic phosphorus forms

Abstract

Twenty surface soil samples, representing two major soil orders alfisols and vertisols were extracted with 0.01N Na₂ EDTA solution (pH 4.8) at a soil/solution ratio of 1:25. Phosphorus in the extract was determined following ammonium molybdate‐stannous chloride colorimetric method. The EDTA extractable P showed significant positive correlations with extractable P according to the Olsen, Morgan, Bray 1 and 2 and also with inorganic phosphorus fractions associated with Al, Ca and Fe.     

The effect of soil flooding on the transformation of Fe oxides and the adsorption/desorption behavior of phosphate

As repeatedly reported, soil flooding improves the availability of P to rice. This is in contrast with an increased P sorption in paddy soils. The effects of soil flooding on the transformation of Fe oxides and the adsorption/desorption of P of two paddy soils of Zhejiang Province in Southeast‐China were studied in anaerobic incubation experiments (submerging with water in N₂ atmosphere). Soil flooding significantly increased oxalate‐extractable Fe (Fe_ox), mainly at the expense of dithionite‐soluble Fe (Fe_DCB), as well as oxalate‐extractable P (P_ox), but decreased the ratio of P_ox/Fe_ox. Flooding largely increased both, P adsorption and the maximum P adsorption capacity. The majority of newly sorbed P in the soils was P_ox, but also more newly retained P was found to be not extractable by oxalate. Flooding also changed the characteristics of P desorption in the soils. Due to a decrease of the saturation index of the P sorption capacity, P adsorbed by flooded soils was much less desorbable than that from non‐flooded soils. There are obviously significant differences in the nature of both, the Fe_ox and P_ox fractions under non‐flooded and flooded conditions. The degree of the changes in Fe_ox, P_ox, P adsorption and P desorption by flooding depended on the contents of amorphous and total Fe oxides in non‐flooded soils. Our results confirm that the adsorption and desorption behavior of P in paddy soils is largely controlled by the transformation of the Fe oxides. The reasons of the often‐reported improved P availability to rice induced by flooding, in spite of the unfavorable effect on P desorbability, are discussed.     

Immobilization of soil copper using organic and inorganic amendments

This experiment aimed to immobilize Cu in polluted agricultural soils via the application of agrochemicals to reduce its bioavailability to plants. A greenhouse pot experiment was established using a Cu contaminated vineyard topsoil collected from a farm in Greece. The soil was mixed with inorganic [i.e., zeolite (Z), Al‐oxide (AX), Mn‐oxide (MX), and phosphate rock (PR)] as well as organic amendments [i.e., activated charcoal (AC), commercial peat soil material (CP), and compost from olive oil processing wastes (COW)] with an application rate of 2.5% and cultivated by corn (Zea maize). After plant harvesting, Cu was measured separately in the aboveground biomass and roots, respectively, whereas the soil samples were analyzed for DTPA‐extractable and geochemical fractions of Cu (soluble + exchangeable fraction, sorbed and carbonate fraction, Fe‐/Mn‐oxides fraction, and organic fraction). The immobilizing agents, except MX, reduced the soluble plus exchangeable Cu in the treated soil. The lowest concentrations of the soluble plus exchangeable Cu occurred in the soil amended with AC followed by CP, AX, COW, PR, and Z, respectively. The amendments decreased the uptake of Cu by corn. Concentrations of Cu were between 11 and 38% lower in the above ground biomass and 19 and 48% lower in the roots than the control. The organic amendments were more effective than the inorganic additives. The AC was the most effective organic additive and AX was the most effective inorganic amendment.     

Evaluation of N,P, S and B fertilization of Kentucky bluegrass seed in northern Idaho

Abstract

Current nitrogen (N) fertilizer recommendations for Kentucky bluegrass (Poa pratensis L.) seed production in northern Idaho are based on potential yield and annual precipitation. Soil test correlation information collected for other northern Idaho crops provide the basis for P, S and B recommendations. The objective of this paper is to assess the current recommendations with a series of forty field trials conducted on ten sites during four seed production seasons. All field trials were conducted on Alfisols and Mollisols initially containing less than 60 kg N/ha, 3.5 μg/g NaOAc extractable P, 40 kg extractable SO₄‐S/ha and 0.5 μg/g extractable B. Fertilization rates evaluated included: 0, 50, 75, 100, 125, 150 and 200 kg N/ha; 0, 30 and 60 kg P₂O₅/ha; 0, 25, and 50 kg SO₄‐S/ha, and 0 and 1.5 kg B/ha. Five field sites contained the cultivar ‘Argyle’ Kentucky bluegrass seed, while the other five sites contained the cultivar ‘South Dakota’.

Excellent relationships between percent maximum Kentucky bluegrass seed production and the sum of inorganic soil N + fertilizer N applied were observed for the ‘Argyle’ (R²=0.65) and ‘South Dakota’ (R²=0.72) cultivars. Phosphorus applications of 30 kg P₂O₅/ha improved seed yields from 10.0 to 51.6% when initial soil test values were less than 3.0 6 μg/g NaOAc extractable P. When initial SO₄‐S soil values were less than 32 kg/ha fertilizer additions increased seed yields from 12.6 to 107.3%. Boron applications did not improve seed yields. Analysis of these trials indicates that adequate information is available to make satisfactory P, S and B fertilizer recommendations; however, additional soil test correlation information is needed for N recommendations.     

Microbial C,N, and P relationships in moisture‐stressed soils of Potohar,Pakistan

In 11 rain‐fed arable soils of the Potohar plateau, Pakistan, the amounts of microbial‐biomass C (C_mic), biomass N (N_mic), and biomass P (P_mic) were analyzed in relation to the element‐specific total storage compartment, i.e., soil C_org, N_t, and P_t. The effects of climatic conditions and soil physico‐chemical properties on these relationships were highlighted with special respect to crop yield levels. Average contents of soil C_org, N_t, and P_t were 3.9, 0.32, and 0.61 mg (g soil)^–1, respectively. Less than 1% of P_t was extractable with 0.5 M NaHCO₃. Mean contents of C_mic, N_mic, and P_mic were 118.4, 12.0, and 3.9 µg (g soil)^–1. Values of C_mic, N_mic, P_mic, soil C_org, and N_t were all highly significantly interrelated. The mean crop yield level was closely connected with all soil organic matter– and microbial biomass–related properties, but showed also some influence by the amount of precipitation from September to June. Also the fraction of NaHCO₃‐extractable P was closely related to soil organic matter, soil microbial biomass, and crop yield level. This reveals the overwhelming importance of biological processes for P turnover in alkaline soils.     

Anion‐exchange membrane,water, and sodium bicarbonate extractions as soil tests for phosphorus

Abstract

Three techniques were evaluated as soil P tests for western Canadian soils: anion‐exchange membrane (AEM), water, and bicarbonate extraction. The AEM, water, and bicarbonate‐extractable total P represented novel approaches to compare to the widely used bicarbonate‐extractable inorganic P (traditional Olsen) soil test. In a range of Saskatchewan soils, similar trends in predicted relative P availability were observed for AEM, water extraction, bicarbonate‐extractable total P, and bicarbonate‐extractable organic P. Correlations between soil test values revealed AEM and water‐extractable P to be most closely correlated, consistent with the similar manner of P removal in the two tests.

Phosphorus availability, as predicted by the tests, was compared to actual P uptake by canola and wheat grown on 14 soils in a growth chamber experiment. P uptake by canola was highly correlated with AEM (r² = 0.86–0.90), water (0.87 ‐0.94), and bicarbonate‐extractable total (0.91) and inorganic (0.92) P. Uptake of P by wheat was not quite as highly correlated with test‐predicted values: AEM (r² = ‐0.73–0.78), water (0.72–0.77), bicarbonate total (0.82), bicarbonate‐inorganic P (0.75).

The similarity in coefficients of determination among test methods indicated nearly identical abilities of the tests to predict soil P availability in the range of soils examined. The AEM and water extractions, unlike bicarbonate, are largely independent of soil type and may prove superior when a wider range of soils is being tested. Bicarbonate‐extractable total P and water‐extractable P suffer limitations in analytical simplicity and cost. In testing for P alone, AEM was considered superior to the other methods due to low cost, simplicity, independence of soil type, and high correlation with plant uptake.     

Comparison of phosphorus availability with application of sewage sludge,sludge compost,and manure compost

Abstract

The objectives were to determine if phosphorus (P) from different organic wastes differs in availability to crops. Four materials: digested, dewatered sewage sludge (DSS); irradiated sewage sludge (DISS); irradiated and composted sewage sludge (DICSS); and composted livestock manure (CLM) were applied for two years at five rates (0, 10, 20, 30, 40 Mg#lbha^‐1#lbyr^‐1) with four replicates. Uptake of P was measured in lettuce [Lactuca saliva L. (cv. Grand Rapids)], bean [Phaseolus vulgaris L. (cv. Tender Green)], and petunia [Petunia hybrida Vilm. (cv. Superior Red)] in 1990, and in consecutively harvested two cuts of lettuce in 1991. Percentage of total P that was extractable by 0.5M sodium bicarbonate (NaHCO₃) in CLM (30–70%) was much higher than in DSS, DISS, and DICSS (0.8–5.6%). Phosphorus uptake by crops harvested in an early stage of growth, lettuce in 1990 and first cut lettuce in 1991, and the extractable soil P linearly increased with total P applied. The lack of response in P uptake with bean pod and petunia in 1990, and the second cut lettuce in 1991, was possibly due to their advanced stage of maturity. Much larger amounts of P were applied with DSS, DISS, and DICSS than with CLM, while P uptake and extractable soil P did not increase compared to that in the treatment that received no P. The low availability of P in sludge was likely caused by iron (Fe) and aluminum (Al) which precipitated P. Sludge irradiation and/or composting had no significant effect on P availability.     

The dynamics of different organic and inorganic phosphorus fractions in soils from the south of Santa Fe province,Argentina

Abstract

The effect of fractioning organic (Po) and inorganic (Pi) phosphorus components on phosphorus form and availability in long‐term cultivation (1) was studied. The study analyzed a Typic Argiudoll soil under three cropping systems: permanent pasture, long‐term cultivation, and mixed pasture and cultivation use. One soil had been cultivated for at least 50 years and one was cultivated for at least 30 years.

The effects of several modifications of these soils were analyzed. Short‐term modifications were determined in a greenhouse experiment in which two successive crops were grown after an initial fertilizer treatment. Long‐term cultivation induced a loss of P, which was considerably greater than the losses of total C or N. Similarly, decreases in pH, extractable P (2), resin‐extractable P, Na‐bicarbonate and Na‐hydroxide Pi, and Na‐bicarbonate Po indicated a long‐term loss of plant‐available Pi with management practices over time.

Increases in some forms of P were observed. Sodium‐hydroxide Po, an organic P form, did not show a significant trend but appeared to increase with years of cultivation. Resin‐extractable Pi was the only fraction that increased significantly as a result of P fertilization.

The relationship observed between dry weight and P concentration of greenhouse plants with the different organic and inorganic P fractions suggests that both types of determinations may be used to predict crop response to P fertilization.     

Compost and P amendments for stimulating microorganisms and maize growth in a saline soil from Pakistan in comparison with a nonsaline soil from Germany

A 92 d greenhouse pot experiment with maize (Zea mays L.) was carried out with a strongly saline soil from Pakistan (P‐s) in comparison with a nonsaline soil from Germany (G‐s) similar in pH and texture. The aim was to evaluate salinity effects on the decomposition of compost and effects of compost and P amendments on (1) plant growth and (2) microbial‐biomass formation. The yield of maize shoot‐C and root‐C increased in both soils in the order nonamended control < +triple superphosphate (TSP) (A1) < +compost (A2) < +(compost + TSP) (A3) < +TSP‐enriched compost (A4). In comparison with the control, the highest yield in treatment A4 was nearly doubled on the G‐s, but was increased more than 8‐fold on the saline P‐s. Averaging the three compost treatments, 32% of the compost added was decomposed in the German soil and 36% in the Pakistani soil on the basis of the compost recovered as particulate organic matter. These data were roughly in agreement with the CO₂‐evolution data. This indicates that the decomposition of compost was not affected by salinity. Compost‐derived CO₂ was mainly evolved until day 32, the root‐derived CO₂ from day 74 until the end of the experiment. The addition of compost resulted in higher contents of microbial biomass C and biomass P, but also in that of NaHCO₃‐extractable P. These three properties were significantly interrelated (r = 0.64–0.85), but on a lower level of significance than the relationships between shoot‐C, root‐C, and NaHCO₃‐extractable P (r = 0.90–0.93). Applying compost enriched with TSP (incubation of compost and TSP for 24 h) provided considerably more P to plants and microorganisms than the separate addition of these two components. The results suggest that the role of the microbial biomass as a sink and source for available P deserves further attention.     

Fertilizer‐use efficiency of different inorganic polyphosphate sources: effects on soil P availability and plant P acquisition during early growth of corn

Polyphosphate‐based fertilizers are worldwide in use, and their effect on crop yield is often reported to be similar to orthophosphate products, although some studies showed higher yields with polyphosphate applications. However, information on how these fertilizers may influence plant P acquisition is very limited. A pot experiment was carried out under controlled conditions with corn (Zea mays L.) growing on a sandy soil (pH 4.9) and a silty‐loam soil (pH 6.9) differing in P‐sorption properties. The objective was to evaluate phosphorus fertilizer–use efficiency (PFUE) of several polyphosphate (poly‐P) compounds (pyrophosphate [PP], tripolyphosphate [TP], and trimetaphosphate [TMP]) using orthophosphate (OP) as a reference. Focus was put on evaluating plant parameters involved in plant P acquisition, i.e., root length and P uptake per unit of root length. Furthermore, soil P availability was characterized by measuring ortho‐P and poly‐P concentrations in soil solution as well as in CAL (calcium‐acetate‐lactate) extracts. The P availability was differentially influenced by the different P sources and the different soils. In the silty‐loam soil, the application of poly‐P resulted in higher ortho‐P concentrations in soil solution. In the same soil, CAL‐extractable ortho‐P was similar for all P sources, whereas in the sandy soil, this parameter was higher after OP application. In the silty‐loam soil, poly‐P concentrations were very low in soil solution or in CAL extracts, whereas in the sandy soil, poly‐P concentrations were significantly higher. Phosphorus fertilizer–use efficiency was significantly higher for poly‐P treatments in the silty‐loam soil and were related to a higher root length since no differences in the P uptake per unit of root length among poly‐P and OP treatments were found. However, in the sandy soil, no differences in PFUE between OP and poly‐P treatments were observed. Therefore, PFUE of poly‐P compounds could be explained by better root growth, thereby improving plant P acquisition.     

Effect of composted sewage sludge amendment on soil nitrogen and phosphorus availability

Abstract

Municipal sewage sludge previously composted with sawdust (CSS) was applied to an eutric sandy cambisol at rates of 7.5, 15.0, 22.5, and 30 g#lbkg^‐1. Incubation and pot experiments were conducted to evaluate CSS effectiveness on nitrogen (N) and phosphorus (P) soil availability and on plant nutrition. The CSS rates did not increase soil mineral N and had little effect on organic P and on labile forms of P. Efficiency of total applied P was 17% for the soil labile forms and 4.8% for the resin extractable fraction. In contrast, CSS significantly increased hydroxide extractable inorganic P and nonextractable soil P fraction. The major portion of the increment on nonextractable forms was at the expense of HC1 extractable P fraction [calcium (Ca)‐bounded], dominant on the original CSS. Thus, chemical rather than biological reactions lead to the redistribution of CSS‐borne P to more firmly held forms after its application to the soil. Ryegrass dry matter yield, N content, and N uptake did not increase in CSS‐treated soils. Plant P content increased at the second harvest, but the effect was nil in the subsequent harvest. Total P uptake increased from 14.1 to 20.2 mg#lbpot^‐1, but percentage P recovery by ryegrass was modest, averaging 2.5% of the CSS‐borne P. Results suggest that moderate application of CSS to agricultural systems are inadequate for crop growth but may contribute to nutrient recycling without environmental risks related to N and P loss.     

Effect of Catch Cropping on Phosphorus Bioavailability in Comparison to Organic and Inorganic Fertilization

ABSTRACT

Phosphorus (P) is a limited resource and its efficient use is a main task in sustainable agriculture. In a 3-year field experiment the effects of catch cropping [oil radish (Raphanus sativus), buckwheat (Fagopyrum esculentum), serradella (Ornithopus sativus), ryegrass (Lolium westerwoldicum), and phacelia (Phacelia tanacetifolia)] of organic fertilization (cattle manure and biowaste compost) and of inorganic fertilization (Triple-Superphosphate) on plant and soil parameters were investigated on a P-poor loamy sand in Northeast Germany. The catch crops were sown in September and remained on the plots until next spring. Then the main crops oilseed rape (Brassica napus), spring barley (Hordeum vulgare), or spring wheat (Triticum aestivum) were cultivated. The yield and P uptake of the main crops were determined. Furthermore, in the soil the organic matter content, pH, phosphorus (P) in soil solution (Psol), double-lactate and oxalate P content, P sorption capacity, and degree of P saturation were measured. All applied forms of fertilizer affected the P contents in soil and the yields and P uptakes of main crops. For green fertilization especially phacelia was found to contribute to the P supply of the main crops, since it increased the P uptake as well as the P contents in soil significantly. The cultivation of ryegrass led to a reduction of the P availability in soil. For example, in average of the three years the Psol content was 0.35 mg L^{? 1}when phacelia was cultivated and 0.22 mg L^{? 1} when ryegrass was cultivated. The cultivation of phacelia had a comparable effect on soil and plant parameters as the organic and mineral fertilization. An improved P availability and P utilization by catch cropping can reduce the need for external P input which may help to save the limited P resources worldwide.     

Influence of Tithonia diversifolia and triple superphosphate on dissolution and effectiveness of phosphate rock in acidic soil

An incubation and a pot experiment were conducted to evaluate the dissolution and agronomic effectiveness of a less reactive phosphate rock, Busumbu soft ore (BPR), in an Oxisol in Kenya. Resin (anion and anion + cation)‐extractable P and sequentially extracted P with 0.5 M NaHCO₃, 0.1 M NaOH, and 1 M HCl were analyzed. Dissolution was determined from the increase in anion resin (AER)–, NaHCO₃‐, and NaOH‐extractable P in soil amended with PR compared with the control soil. Where P was applied, resin P significantly increased above the no‐P treatment. Busumbu‐PR solubility was low and did not increase significantly in 16 weeks. Anion + cation (ACER)‐extractable P was generally greater than AER‐P. The difference was greater for PR than for triple superphosphate (TSP). The ACER extraction may be a better estimate of plant P availability, particularly when poorly soluble P sources are used. Addition of P fertilizers alone or in combination with Tithonia diversifolia (TSP, BPR, TSP + Tithonia, and BPR + Tithonia) increased the concentration of labile inorganic P pools (NaHCO₃‐ and NaOH‐P_i). Cumulative evolved CO₂ was significantly correlated with cumulative N mineralized from Tithonia (r, 0.51, p < 0.05). Decrease in pH caused NH ‐N accumulation while NO ‐N remained low where Tithonia was incorporated at all sampling times. However, when pH was increased, NH ‐N declined with a corresponding rise in NO ‐N. Tithonia significantly depressed soil exchangeable acidity relative to control with time. A significant increase (p < 0.05) was observed for P uptake but not dry‐mass production in maize where BPR was applied. The variations in yield and P uptake due to source and rates of application were statistically significant. At any given P rate, highest yields were obtained with Tithonia alone. Combination of Busumbu PR with TSP or Tithonia did not enhance the effectiveness of the PR. The poor dissolution and plant P uptake of BPR may be related to the high Fe content in the PR material.     

Availability of Organic and Inorganic Phosphorus Fractions to Wheat in Toposequences of Calcareous Soils

Abstract

Information on the availability of different soil phosphorus (P) forms is useful for crop production. Phosphorus contents of 12 Iranian calcareous soils from upper‐, mid‐, and lower‐slope positions of two arid and two semiarid toposequences were fractionated to various organic and inorganic pools, and correlations of the P fractions with wheat responses were investigated. Among the inorganic P (IP) fractions, apatite type (Ca₁₀‐P) and dicalcium phosphate equivalents (Ca₂‐P) possessed the highest and the lowest amounts of P reserve in the soils, respectively. On average, about 20% of the total P was found in organic form (OP), of which 32% was labile (LOP), 51% was moderately labile (MLOP), and 17% was nonlabile (NLOP). The amounts of the soil P fractions were considerably influenced by the positions of the soils on the landscapes. The maximum contents of soil IP, Ca₂‐P, Fe‐P (iron‐bound P), and Ca₁₀‐P were observed in the lower‐slope positions. The amount of soil available [0.5 M sodium bicarbonate (NaHCO₃) extractable] P was significantly correlated with Ca₂P (r=0.895), Fe‐P (r=0.760), and Occl‐P (iron‐occluded P) (r=0.897). Direct correlation studies, however, showed that wheat shoot dry‐matter yield (DMY) was significantly affected by the amounts of Ca₂‐P, Fe‐P, OP, LOP, and MLOP fractions both at early (4 weeks) and late (10 weeks) stages of growth. All organic and inorganic P fractions, except Al‐P (aluminum‐bound P), Ca₈‐P (octacalcium phosphate equivalents), and NLOP, also showed significant relations to the amount and/or concentration of P in wheat tissues at 4 and 10 weeks after sowing. Among the measured soil properties, the amount of organic carbon was the most affecting factor on the size of the P fractions.     

Wheat p requirements on calcareous Morrocan soils: III evaluation by isotherms compared to Olsen extractable P

Abstract

Phosphorus fertilizer recommendations were compared by interpretations from P isotherms, Olsen extractable P and the Mitscherlich‐Bray model based on the Olsen method for 15 soils from the Chaouia (dryland) region of Morocco. The P isotherms were fit to straight line and second degree polynomial equations. The P buffer indexes (PBI) derived from the isotherms were not significantly correlated to P buffer capacities as measured by a single P buffer capacity index, but negatively correlated to Olsen P (r = ‐0.63), relative yield (r = ‐0.76) and P uptake (r = ‐0.66). Phosphorus in solution was a quadratic function of P added in 0.01 M CaCl₂equilibrium solution. The P fertilizer recommendations to maintain soil solution P concentrations at 0.01, 0.12 and 0.20 mg P L^‐1were higher than recommended by direct interpretation of plant response to Olsen extractable P and the quantity based on the Mitscherlich‐Bray model as calculated from Olsen available P values. The P fertilizer recommended to maintain soil solution P of 0.10 mg P L^‐1was significantly correlated with Olsen P (r = 0.71) as was that recommended Mitscherlich‐Bray log transformation model (r = 0.81), and nonlinear least square estimation (r = 0.78). Field research will be needed to evaluate if the P fertilizer recommended to maintain this solution P concentration is adequate for maximum economic wheat grain yield under field conditions