固、液态磷源在石灰性土壤中的移动性及其对土壤有效磷含量影响的研究

采用同心圆扩散法对固体和酸性液体磷肥在石灰性土壤中的移动性与有效性进行研究。结果表明,土壤Olsen-P含量随施肥点圈层由内向外层而递减,液肥处理的Olsen-P量在施肥点以外的3个土壤圈层中均高于固肥处理。固体肥料大部分停留在距施肥点0~7.5 mm圈层,占施磷总量的55%~70%;液体肥料虽在0~7.5 mm层的含量低于固体肥料(约占15%~40%),但在远离施肥点的后3个圈层(7.5~43 mm)中均高于固体肥料处理,其中7.5~13.5 mm最为明显(液肥占35%,固肥占20%)。3种施磷量在砂土、壤土及粘土上均表现出一致的变化规律。肥料对土壤pH值的影响仅限制在距施肥点最近的0~7.5 mm范围,该层的pH值显著低于后层。本研究说明在石灰性土壤中液体磷的移动性、有效性明显高于固体磷,但对土壤pH值无显著影响。     

Assessment of the effect of time and temperature on the availability of residual phosphate in a glasshouse study of four soils using the Olsen method

Abstract. The Olsen method is an indicator of plant-available phosphorus (P). The effect of time and temperature on residual phosphate in soils was measured using the Olsen method in a pot experiment. Four soils were investigated: two from Pakistan and one each from England (calcareous) and Colombia (acidic). Two levels of residual phosphate were developed in each soil after addition of phosphate by incubation at either 10 °C or 45 °C. The amount of phosphate added was based on the P maximum of each soil, calculated using the Langmuir equation. Ryegrass was used as the test crop. The pooled data for the four soils incubated at 10 °C showed good correlation between Olsen P and dry matter yield or P uptake ( r ²= 0.85 and 0.77, respectively), whereas at 45 °C, each soil had its own relationship and pooled data did not show correlation of Olsen P with dry matter yield or P uptake. When the data at both temperatures were pooled, Olsen P was a good indicator of yield and uptake for the English soil. For the Pakistani soils, Olsen P after 45 °C treatment was an underestimate relative to the 10 °C data and for the Colombian soil it was an overestimate. The reasons for these differences need to be explored further before high temperature incubation can be used to simulate long-term changes in the field.     

不同农业土壤中有效磷的变化与磷平衡的关系

Maintaining soil phosphorus(P) at adequate levels for plant growth requires assessing how the long-term P balance(viz., the difference between P inputs and outputs) results in changes in soil test P. The hypothesis that routinely measured soil properties can help predict the conversion factor of P balance into Olsen P was tested at 39 sites in agricultural areas of the Mediterranean region in Spain. A set of soil samples from each site was analyzed for Olsen P, inorganic P(P extracted using 0.5 mol L~(-1) H_2SO_4), pseudototal P(P extracted using 0.5 mol L~(-1) H_2SO_4 following ignition at 550℃), and organic P(the difference between pseudototal P and inorganic P). Organic and Olsen P were uncorrelated in most of the 39 soil sets, which suggests that organic P content changed little with P inputs and outputs. The slopes of the regression lines of Olsen P against pseudototal and inorganic P, which were used as two different measures of the conversion factor, ranged widely(from 0.03 to 0.25 approximately), with their average values(about 0.10) being similar to those found in long-term experiments conducted in temperate areas. Neither conversion factor was significantly correlated with any routinely measured soil property; however, the conversion factor for inorganic P was significantly lower for calcareous soils than for noncalcareous soils. Our negative results suggest the need to isolate the influence of soil properties from that of management systems and environmental factors relating to P dynamics in future studies.     

Transformation kinetics of inorganic P forms in relation to calcareous soil properties of western Iran

This study was conducted to investigate the effect of time on chemical forms of P in 10 calcareous soils of western Iran. Phosphorus was added to soils at the rate of 200 mg kg^?1 as KH₂PO₄. The samples were incubated for 1, 7, 15, 30, 60, 90 and 120 days at 25°C and constant moisture. After incubation, P was fractionated by the sequential extraction procedure: soluble and exchangeable P (NaHCO₃-P) Al + Fe-P (NaOH-P), Ca-P (HCl-P) and residual P (Res-P). The distribution of added P into different fractions consisted of two phases involving initial rapid retention followed by a slow continuous retention. In general, the majority of the P applied entered mostly in the HCl-P and Res-P fractions. After 120 days incubation, the HCl-P fraction remained the most dominant in all soils. A combination of silt and sand content of the soils together explained between 88.5 and 83.3% of the variance inNaHCO₃-P and HCl-P transformation rates, respectively, 76.6 and 72.8% of which is explained by silt alone. CaCl₂-P and electrical conductivity (EC) together accounted for 66.3% of the variation in the rate constant of NaOH-P. The release rate of Res-P was not significantly related to soil properties.     

Kinetics of nonexchangeable‐potassium release and plant response in some calcareous soils

Nonexchangeable K⁺ constitutes a slowly available reserve that may significantly influence K⁺ fertility of soils. Laboratory and greenhouse experiments were conducted to characterize the K⁺ supply and nonexchangeable K⁺–release kinetics in 10 calcareous soils using 0.01 M CaCl₂ and 0.01 M oxalic acid extractions. Total K⁺ uptake by wheat (Triticum aestivum L.) grown in the greenhouse was used to measure plant‐available K⁺. The release of K⁺ was characterized by an initial fast rate followed by a slower rate. The nonlinear relationship in the early stages of the K⁺ release may be attributed to the edge sites, and release of K⁺ from interlayer exchange sites may be responsible for the second part of the K⁺ release. Kinetics of K⁺ release was described best with power function, which showed the best fit of the four models tested. Parameters of kinetics models in 0.01 M CaCl₂ were significantly related to K⁺ uptake by wheat. Potassium release was also correlated to initial NH₄OAc‐extratable K⁺ and to HNO₃‐extractable K⁺.     

石灰性水稻土中磷酸铁对水稻磷营养的贡献

A study was carried out on contribution of iron phosphate to phosphorus nutrition of rice plant under waterlogged and moist conditions,respectively,by use of synthetic Fe^32 PO4.nH2O,tagging directly the iron phophate in calcareous paddy soils.Results showed that under waterlogged condition,similar to iron phosphate in acidic paddy soils.that in clacareous paddy soils was an important source of phosphorus to rice plant ,and the amount of phosphorus originated from it generally constituted 30-65% of the total phosphorus absorbed by rice plant.     

Labile pools of copper and zinc in calcareous soils as measured by DTPA and plant extraction

Abstract

Labile pools of Cu and Zn were measured on two calcareous soils from Saudi Arabia, using successive extraction with DTPA, and successive cropping followed by extraction with DTPA after cropping. The examined soils differed in their ability to supply Cu and Zn. The first DTPA extraction removed a major proportion of the labile pool, particularly in the sandy soil. The two soils showed a general decrease in extractable Cu and Zn with progressive extractions, with DTPA extractable Cu declining more rapidly than Zn. DTPA extractable Cu and Zn determined after cropping were highly correlated with DTPA extractable Cu and Zn values obtained after successive extractions. The results gave evidence on both the contribution of element dissolution from insoluble forms with progressive extraction or cropping, and the usefulness of the DTPA extractant for monitoring the availability of Cu and Zn in these calcareous soils.     

Influence of soil applied boron on yield of berseem (Trifolium alexandrium L.) and soil boron fractions in calcareous soils

A greenhouse experiment was conducted in North-west India to study the effect of soil applied boron on yield of berseem (Trifolium alexandrium L.) and soil boron fractions in boron deficient calcareous soils. Three soils with varying calcium carbonate content viz. 0.75% (Soil I), 2.6% (Soil II), and 5.7% (Soil III) were collected from different sites of Ludhiana, Bathinda, and Shri Muktsar Sahib districts, Punjab, India. The treatments consisted of six levels of soil applied boron viz. 0.5, 0.75, 1.0, 1.25, 1.5, and 2.0 mg B kg^?1 along with control. The green fodder yield and dry matter yield increased significantly at 0.75 mg B kg^?1 soil treatment level in the first cutting, while these were significant at 1.0 mg B kg^?1 soil treatment level in all soils at second, third, and fourth cuttings. Among all three calcareous soils, Soil I with lower calcium carbonate was the best soil in respect of mean yield in comparison to Soil II and Soil III. Combined effect of boron level and soils had significant effect on yield of berseem. There was a significant increase in mean dry root biomass at 1.0 mg B kg^?1 soil level over control and then remained non-significant with further high levels of soil applied boron. The mean dry root biomass decreased significantly for the soils having 0.75%, 2.6%, and 5.7% calcium carbonate levels. Readily soluble fraction is considered to be easily available fraction of B for plant uptake and consisted of 0.47–0.62% in Soil I, 0.31–0.43% in Soil II, and 0.24–0.34% in Soil III of the total boron. Among all B fractions, mean readily soluble, specifically adsorbed, and oxide-bound fractions got increased significantly with increase in B levels. Readily soluble and organically bound B fractions were more in Soil I as compared to Soil II and Soil III. Specifically adsorbed boron, oxide bound fraction, residual and total boron were more in Soil III in comparison to Soil I and Soil II. Among all fractions, residual fraction accounted for the major portion of the total B. It comprised of 92.71–93.90% in Soil I, 94.51–95.40% in Soil II, and 94.91–95.25% in Soil III of the total boron.     

Potassium release from sand,silt and clay fractions in calcareous soils of southern Iran

The release of non-exchangeable potassium from 24 calcareous soils of divergent mineralogy, from southern Iran, was examined. Sand, silt and clay particles were fractionated after dispersion with an ultrasonic probe. Samples were extracted with 0.01 M CaCl₂ for 30 successive 2-h periods. The clay fraction released the largest amount of K in each soil. Cumulative K released ranged from 175 to 723, 35 to 128, and 71 to 146 mg kg^?1 contributing 20–90, 4–39 and 2–54% for clay, silt and sand fractions, respectively. The lower proportion of K released from sand and silt fractions can be explained by the presence of a high content of CaCO₃ and quartz in these fractions. The release kinetics for the non-exchangeable K data showed that parabolic diffusion and power function were the best fitting kinetic models. This indicated that slow diffusion of K from the mica interlayer positions is the main rate-controlling process. Cumulative K released and constant b values of parabolic diffusion model correlated significantly with the mica content of the clay fraction.     

The effect of pig slurry on exchangeable potassium in calcareous soils

Pig slurry in quantities of 200, 400, 500, 600, 800, and 1000 m³ ha^-1 year^-1 was added to two calcareous soils, which differed in concentration and type of clay minerals. The soils were cultivated with two successive crops of pepper and tomatoes grown in containers. A control was given no slurry. The soils were analysed after harvesting for exchangeable K⁺. Differences in exchangeable K⁺ were studied in relation to the concentration and type of clay minerals. The soil with the higher clay content and of the illite type retained K in the exchangeable form to a much greater extent than the soil with the low clay content. In the soil with the lower clay content, of the interstratified illitic — montmorillonite type, very little K was incorporated into the exchange complex. The exchange capacity being low, the amount of K added had little effect on the level of exchangeable K⁺.     

The effect of organic amendments on mineral phosphate fractions in calcareous soils

Organic amendments considerably affect nutrient balance and interfraction mobility of nutrients by influencing the chemical, physical, and biological environment in soils. In this study, the effects of five amendments including: two composts, farmyard manure, packaging‐industry by‐product, and olive‐mill waste on time‐dependent interfraction mobility of P among mineral P fractions in two semiarid‐region soils differing in carbonate content and texture were investigated. Organic materials were applied at the rate of 0, 25, 50, and 100 g (kg soil)^–1 soil thoroughly mixed and incubated at 27°C ± 2°C for 110 d. Phosphorus fractions were sequentially extracted by 0.1 M NaOH + 1 M NaCl (NaOH‐P), citrate‐bicarbonate‐dithionite (CBD‐P), and 0.5 M HCl (Ca‐P). Results showed that organic amendments especially farmyard manure significantly influenced NaOH‐P, CBD‐P, and Ca‐P. In addition, higher application rates of organic residues increased NaOH‐P fraction. NaOH‐P and CBD‐P fractions were increased after addition of organic residues and then converted to Ca‐P fraction within the end of incubation period. Increasing application rate of organic residues allowed P to be retained in more labile fractions for a longer period. The amount of Ca‐P was found to be related with carbonate content of soils. It can be concluded that organic residues applied to calcareous soils may enhance P nutrition of agricultural plants.     

Evaluation of preflooding effects on iron extractability and phytoavailability in highly calcareous soil in containers

Previous pot cropping and laboratory incubation experiments were consistent with field observations showing that temporary flooding before cropping can increase the availability of soil Fe to plants. To study the effect of temporary flooding on changes in soil Fe phytoavailability we used 24 highly calcareous, Fe chlorosis–inducing soils to carry out a pot experiment where peanut and chickpea were successively grown after flooding for 30 d. At the end of the cropping experiment, the preflooded soil samples exhibited higher concentrations of acid oxalate‐, citrate/ascorbate‐ and diethylenetriaminepentacetic acid (DTPA)–extractable Fe (Fe_ox, Fe_ca, and Fe_DTPA, respectively) than the control (nonflooded) samples. Also, Fe_ox and Fe_ca exhibited no change by effect of reflooding of the cropped soils or three wetting–drying cycles in freeze‐dried slurries of soils previously incubated anaerobically for several weeks. Leaf chlorophyll concentration (LCC) in both peanut and chickpea was greatly increased by preflooding. The best predictor for LCC was Fe_ox, followed by Fe_ca and Fe_DTPA. The LCC–soil Fe relationships found suggest that the Fe species extracted by oxalate and citrate/ascorbate from preflooded soils were more phytoavailable than those extracted from control soils. However, the increased phytoavailability of extractable Fe forms was seemingly limited to the first crop (peanut). Flooding dramatically increased Fe_DTPA; however, high Fe_DTPA levels did not result in high LCC values, particularly in the second crop. Therefore, this test is a poor predictor of the severity of Fe chlorosis in preflooded soils.     

Phosphorus-induced zinc deficiency in wheat pot-grown on noncalcareous and calcareous soils of different properties

High levels of phosphorus (P) often induce zinc (Zn) deficiency in plants grown on Zn-poor soils. We investigated P-induced Zn deficiency in durum wheat (Triticum durum L. ‘Carpio’) grown on 16 noncalcareous and 31 calcareous soils differing in levels of available (Olsen) P and available (diethylenetriaminepentaacetic acid (DTPA)-extractable) Zn using micropots. A completely randomized factorial design with two levels of P (0 and 40 mg P kg^?1 soil) and Zn (0 and 3 mg Zn kg^?1 soil), i.e. four treatments (‘control’, + P, + Zn, and + PZn), were used. Grain yield of control plants depended mainly on the Olsen P level. Phosphorus had a negative effect on yield in 6 soils with Olsen P/Zn_DTPA > 25, and Zn a positive one in 5 soils with Olsen P/Zn_DTPA > 50; and the + PZn treatment generally resulted in the highest yield. Grain Zn concentration of control plants was negatively correlated with growth and Olsen P. Calcareous soils were less sensitive to P-induced Zn deficiency than noncalcareous soils because phosphate is sorbed by calcite rather than being co-adsorbed with Zn on the Fe oxides. Co-application of P and Zn to soil at low and application of Zn at high Olsen P ensured both maximum yield and grain Zn bioavailability.     

Phosphate adsorption by soils 1. Influence of time and ionic environment on phosphate adsorption

Abstract

The influence of reaction time and ionic environments, on phosphate adsorption were studied using one calcareous soil from India, and one calcareous and two latosols from Hawaii.

Phosphorus adsorption by soils has a initial rapid phase followed by a slow process. For plant nutrition studies, where emphasis is on P concentration of solutions from which plants derive P, isotherms should be constructed using data obtained after near‐equilibration has been attained. This condition does not obtain in a few hours and may require 6 days or more.

Calcium chloride as suspending electrolyte always gave lower phosphate solubility than when KC1 was used as electrolyte. Phosphate retention increased with increasing ionic strength. The necessity for obtaining clear supernatant solutions and the desirability for maintaining reasonable constant equilibrium conditions make 0.01 M CaCl₂ a reasonable choice for constructing P sorption isotherms, even though 0.01 M CaCl₂ is not representative of Ca concentrations in many soil solutions. Saturation extracts of soils investigated here were in the range 0.0002 to 0.005 M Ca.

Adsorption of calcium by highly weathered soils was high suggesting specific adsorption. Calcium adsorption was increased by phosphate additions to a Hydrandept.     

Changes in recovery of native and applied phosphorus with time as affected by soil properties in some calcareous soils

In an attempt to investigate variations in availability of native and applied phosphorus (P) with time, twenty five calcareous soil samples were treated with 0, 50 and 500 mg P kg^?1 soil and incubated at 80–90% of field capacity moisture content in an open door glasshouse for a period of one year. Soil samples were taken out at certain intervals for P extraction with Olsen extractant under moist condition. Results indicated that following wetting the mean value of native Olsen-P decreased initially and then increased gradually with time of incubation. Generally, the short term (24 h) recoveries were not correlated with long term ones. The recovery of added P with time was described properly by the following new proposed model: R = 100/(1 + kt^b), where R is percent recovery at time t, and k and b are empirical parameters. The values of k constant at 50 and 500 mg P kg^?1 were in the ranges of 0.40 to 1.22 (0.84 ± 0.25, on average) and 0.04 to 0.52 (0.23 ± 0.14, on average), respectively. The corresponding respective values of b constant also ranged from 0.05 to 0.32 (0.15 ± 0.06, on average) and 0.12 to 0.92 (0.46 ± 0.23, on average).     

Availability and plant uptake of nutrients following the application of paper pulp and lime to tropical acid soils

Availability and plant uptake of nutrients were evaluated in three tropical acid soils (Kandiudult) amended with paper pulp and lime under greenhouse conditions. Amendments were applied to attain target pH values of 5.5, 6.0, and 6.5. A control treatment (no paper pulp or lime added) was also included. Rye grass (Lolium perenne L.) as a test plant was grown for three successive cycles of 40 days each. Extractable nutrients and cumulative nutrient uptake were determined. The application of paper pulp or lime resulted in a significant increase in exchangeable Ca and K and a decrease in exchangeable Mg and extractable Fe, Mn, and Zn. Amendment of soils with paper pulp or lime increased plant uptake of Ca and Mg and decreased that of K, Mn, and Zn. Both amendments behaved similarly, but the effect of lime seemed generally greater than that of paper pulp. Paper pulp in tropical acid soils behaved as a liming agent rather than an organic amendment. Similar to lime, amendment of soils with paper pulp resulted in an increase in availability of Ca and Mg and in a decrease in availability of K, Mn, and Zn for plants. Soil extractions appeared to be appropriate for assessing the availability of Ca, Mn, and Zn. Soil pH and effective cation exchange capacity positively influenced the availability of Ca and negatively the availability of Mn and Zn. Thus, the precision of predicting nutrient availability in paper pulp amended tropical acid soils could be improved by including soil pH or effective cation exchange capacity in relevant regression equations.     

Competitive and noncompetitive adsorption of silicate and phosphate by two acid Si-deficient soils and their effects on P and Si extractability

The effects of pH on the adsorption of silicate and phosphate, either singly or in competition, by two acid soils were investigated. Both soils adsorbed two to three times more P than Si and adsorption isotherms at pH 5.0, 5.5, 6.0 and 6.5 showed that increasing pH greatly increased Si adsorption but decreased that of P. Silicate adsorption was very low below pH 5.0, increased rapidly up to pH 9–10 before decreasing again. Adsorption of P was at a maximum at pH 2.0, decreased slowly up to pH 7.0 and then more rapidly above pH 7.0. When Si and P were added at equimolar concentrations, the presence of P decreased Si adsorption between pH 6.0 and 8.0 while the presence of Si decreased P adsorption in the pH region 6.0 and 11. Addition of calcium silicate at rates equivalent to 300, 600 and 1200 kg Si ha^?1 resulted in a progressive increase in soil pH. Separate samples of soil were treated with Ca(OH)₂ to give the same pH values so that the effect of Si could be identified. The highest rate of Si (1200 kg ha^?1 which gave a pH of 6.5) caused a significant decrease in P adsorption (as determined by adsorption isotherms) and an increase in resin-extractable P but the lower rates had little effect. Addition of P to the soil as calcium phosphate at rates equivalent to 30, 60 and 100 kg P ha^?1 all caused a decrease in Si adsorption capacity and an increase in CaCl₂-extractable Si. It was concluded that the strategy of adding Si to lower P requirements in acid soils is not likely to be effective while addition of fertilizer P may well lower Si adsorption and promote Si desorption and its increased mobility.     

Band-applied elemental sulfur to enhance the phytoavailability of phosphorus in alkaline calcareous soils

Summary Applications of elemental sulfur (S°) increase the phytoavailability of P in alkaline high-Ca soils through the production of H₂SO₄ which is induced by microbial oxidation of S. Concentrated S bands, allowing time release acidity, may aid in maintaining the phytoavailability of both residual and fertilizer P. Greenhouse and field studies were therefore conducted to determine the effectiveness of band-applied S° for increasing the phytoavailability of residual and fertilizer P for spring wheat (Triticum aestivum L.) and corn (Zea mays L.). We also used inoculation of S° with Thiobacillus thioparus to determine whether it is necessary or helpful in alkaline soils to initiate acidification. Treatments were inoculation, S°, S° + inoculation, triple superphosphate, triple superphosphate + S°, triple superphosphate + inoculation, and triple superphosphate + S° + inoculation applied to three alkaline soils: Typic Argiborolls, Borollic Calciorthids, and Ustollic Haplargids. P availability was determined by plant uptake of P, NaHCO₃-extractable P, dry-matter yield, grain yield and grain-protein production, and on available-P index (NaHCO₃-extractable P, post-harvest, + plant uptake of P). Application of S° with triple superphosphate gave a significantly higher available-P index than triple superphosphate alone on all three soils. Inoculation of S° with T. thioparus increased soil acidity; however, in some cases this treatment eliminated the beneficial effect of S°. Grain yields of wheat increased with S° applications at one of two field sites. These results suggest that applying S° with triple superphosphate may be an effective means of increasing soil P availability and the efficiency of superphosphate fertilizers on alkaline high-Ca soils.