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1.
Abstract

Two single value methods of indexing P sorption were compared to parameters derived from P adsorption isotherms in a range of waterlogged and dry rice soils. These measures of P sorption capacity correlated closely with one another. However, they did not correlate equally with several other soil properties (pH, extractable Fe and Al). Because relationships between P sorption and soil properties proved to be method dependent, results from different methods must be compared with caution.

It is suggested that the single value method of Bache and Williams2 be adopted when the rapid analyses of many samples is required. It is suited to routine analysis of soils with markedly different P sorption capacities, from both waterlogged and dry conditions.

Close correlations between the single value methods and P sorbed at a standard supernatant concentration suggest they may be useful in testing soils for P fertilizer requirements.  相似文献   

2.
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 (Feox), mainly at the expense of dithionite‐soluble Fe (FeDCB), as well as oxalate‐extractable P (Pox), but decreased the ratio of Pox/Feox. Flooding largely increased both, P adsorption and the maximum P adsorption capacity. The majority of newly sorbed P in the soils was Pox, 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 Feox and Pox fractions under non‐flooded and flooded conditions. The degree of the changes in Feox, Pox, 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.  相似文献   

3.
Abstract

Standardization of the P soil test procedures is desirable; however, both NaOAc and NaHCO3 are currently used to extract P from soils in the Pacific Northwest region of the USA. The purpose of this study was to determine the relationship between NaOAc and NaHCO3 extractable P in soils and to evaluate the effect of plant material on this relationship in a northern Idaho soil. The Ap horizon of a Latahco silt loam was used and alfalfa (Medicago sativa), pea (Pisum sativum) and wheat (Triticum aestivum) plant materials were added as amendments at rates of 0%, 1%, 5% and 10% (w/w). The soils were incubated for 20 weeks under controlled conditions. In addition, other parameters studied included soil water potential (‐0.05, ‐0.15 and ‐0.40 MPa), incubation temperature (10, 20 and 30°C and incubation period. P in samples was extracted by NaOAc and NaHCO3 extractants. A statistically significant linear relationship between NaOAc and NaHCO3 extractable P was observed (r2 = 0.96). In addition, the types of plant residues added to soil differently affected P extraction by the two extractants. The difference between NaOAc and NaHCO3 extractable P was greatest in the wheat material treatment while alfalfa material resulted in the smallest effect. Sodium acetate extractable P values increased faster than NaHCO3 extractable P with increasing amendment rate.

A simple regression relationship will allow conversion between NaOAc and NaHCO3 extractable P in the Latahco soil. Additions of less than 5 mt/ha plant material will have a minimal impact on this relationship.  相似文献   

4.
Contaminated riparian soils can release metals to surface water. Periodic waterlogging affects metal mobility but the processes and soil factors governing net trends are not well understood. Experiments were combined with geochemical modelling to identify processes explaining the dynamics of zinc (Zn) in contaminated soils following waterlogging. Samples were collected from 12 Spodosols near streams in a metal‐contaminated area and four similar but uncontaminated soils were sampled in a reference area. Air‐dried samples were submerged and incubated under N2. The soil redox potential decreased from 470 mV initially to approximately 30 mV over 2 months. The pore‐water Zn concentrations surprisingly increased over the same period by, on average, a factor of 18 (range 0.6–80; immobilization in one soil only) despite an increase in pH of 1.8 units, on average. Dissolved organic matter (DOM) in the soil solution increased during waterlogging but the observed increase in Zn solubility could not be explained by increased complexation with DOM, because the estimated Zn2+ activity also increased by a factor of 18 on average (range 0.2–82). Speciation modelling suggests that Zn mobilization during waterlogging results from Fe2+ displacing sorbed Zn2+ from particulate organic matter and from dissolution of Zn‐bearing Fe/Mn oxyhydroxides. This hypothesis is supported by the significant positive correlation (r = 0.87, n = 13) between the factor change in pore‐water Zn concentration and the ratio of dithionite‐extractable Fe to organic carbon content. These results show that Fe dynamics are important for predicting the fate of trace metals in anoxic soils.  相似文献   

5.
氧化还原条件对土壤磷素固定与释放的影响   总被引:35,自引:2,他引:35  
张桃林  高超  吴蔚东 《土壤学报》2002,39(4):542-549
为探讨水稻土由氧化环境转为还原条件时对土壤磷素固定与释放的影响,选择18种水稻土样品进行室内模拟实验,通过测定不同条件下磷的等温吸附曲线和采用氧化铁试纸测定法进行多次提取以对比淹水前后土壤磷的累计解吸量,发现大部分供试样品的固磷能力在淹水条件下有了显著的提高,全部样品在淹水后磷的释放量都有不同程度的减少。进一步的研究表明淹水条件下土壤对磷的固定与释放的变化主要与淹水后土壤Eh的降低和pH的升高而导致的大量无定形铁的形成有关。  相似文献   

6.
Waterlogging results in high shoot concentrations of iron (Fe), aluminum (Al), and manganese (Mn) in wheat grown in acidic soil. The verification of this observation in several acidic soils, development of screening techniques, and identification of genotypes differing in tolerance made it possible to test whether tolerance of ion toxicities improves performance of wheat in waterlogged acid soils. Six wheat varieties selected for tolerance/intolerance of Al, Mn, and Fe were grown in three acidic soils (pHCaCl2 4.1–4.3) with or without waterlogging for 40 d. In terms of relative shoot dry weight, Al‐, Mn‐, and Fe‐tolerant genotypes tolerated waterlogging better, outperforming intolerant genotypes by 35%, 53%, and 32%, respectively, across the soils. The Al‐tolerant genotype had up to 1.8‐fold better root growth than the intolerant genotype under waterlogging. Waterlogging increased DTPA‐extractable soil Mn (71%) and Fe (89%), and increased shoot Fe (up to 7.6‐fold) and Al (up to 5.9‐fold) for different genotypes and soils. The Al‐tolerant genotype maintained lower tissue concentrations of Al as compared to intolerant genotypes during waterlogging. Waterlogging delayed crop development but distinctly less so in the tolerant than in the intolerant genotypes, thus jeopardizing the capacity of intolerant genotypes to produce yield in Mediterranean climates with dry finish of the season. Pyramiding multiple ion tolerances into current wheat varieties with desirable agronomic and quality characteristics to enhance their performance under waterlogged acid soils should be considered.  相似文献   

7.
Abstract

Phosphate (P) sorption characteristics of six natural Ghanaian Oxisols, selected because of their hydrological and topographical suitability for agriculture, were evaluated. Availability of P appears to be adequate for half of the soils as suggested by the Bray P1 test and determination of the standard P requirement (SPR), i.e., the amount of P sorbed at a concentration of 0.2 ppm P (6.46 μM). The SPR was found to be very closely related to Pmax (Langmuir P sorption capacity), which in turn, was significantly correlated with oxalate‐extractable aluminum (Al) (Alo) and iron (Fe) (Feo) and related (not significantly) to the difference between dithionite‐citrate‐bicarbonate‐extractable Fe (Fed) and oxalate‐extractable Fe. Accordingly, Pmax is fairly well predicted by the model of Borggaard: Pca]e=0.211#lbÀlo+0.115#lbFeo+ 0.05#lb(Fed‐Feo)+0.3, except for one soil strongly enriched in Fe oxides, mainly goethite. This goethite was found by X‐ray diffraction analysis to consist of crystals larger than normally found for pedogenic Fe oxides. The difference between Pmax and Pcalc for this soil could, therefore, be attributed to the occurrence of these large Fe oxide crystals, because P sorption will decrease with increasing crystal size (decreasing specific surface area).  相似文献   

8.
Phosphate sorption was studied in samples (0 - 20 cm depth) of five soils from Egypt (pH 7.4 - 8.7), four soils from Ethiopia (pH 3.9 - 5.3) and six soils from Germany (pH 3.3 - 7.2). Sorption parameters were calculated according to Pagel and Van Huay (1976) and according to Langmuir (Syers et al., 1973). Phosphate sorption parameters and oxalate extractable Fe and Al (Feox, Alox) were related to the phosphate uptake by young rye plants in Neubauer pot experiments. P sorption parameter after Pagel and Van Huay (A) correlated significantly positively with the Feox and Alox content in acid (r = 0.73) as well as in calcareous soils (r = 0.89) if the whole equilibrium concentration range (0 - 14 mg P/L) was considered. The relations calculated after Langmuir (B) were similar. P uptake by rye in acid soils was negatively correlated with the affinity constant n (r = ?0.76, (A)). In calcareous soils, a negative correlation between P uptake and affinity constant was calculated in the lower P equilibrium range (0 - 2.8 mg P/L) only for (B). Thus, P uptake decreased with increasing strength of P bonding to soil. From these results it is concluded that phosphate sorbed to Fe/Al oxides is an important P source for plants in acid and calcareous soils.  相似文献   

9.
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 (Feox, Feca, and FeDTPA, respectively) than the control (nonflooded) samples. Also, Feox and Feca 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 Feox, followed by Feca and FeDTPA. 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 FeDTPA; however, high FeDTPA 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.  相似文献   

10.
Flocculation and dispersion of colloidal particles of nine inorganic paddy soils were studied mainly based on turbidity measurements of the suspensions of soils which were previously incubated at 28°C under in vitro waterlogged conditions. After 1-week of incubation, the turbidity of the soils except for 1) two soils containing larger amounts of sodium salts and 2) one soil containing larger amounts of Fe and Al oxides, significantly decreased, and colloidal particles flocculated with 1) a decrease in soil Eh and 2) an increase in electric conductivity (EC). During the 3- to 4-week period of waterlogging, the turbidity of the three soils significantly increased with the 1) decrease in EC and 2) increase in pH of the soils although the Eh remained low. Infrared (IR) absorption analysis showed that the suspended colloidal particles consisted of layer silicates from respective soil clays. Oxidation of suspensions of waterlogged soils by air-bubbling led to an increase in turbidity with the 1) increase in Eh, and 2) decrease in pH, EC, and water-soluble Fe2+ concentration. It was suggested that the stability of the soil colloidal suspensions was affected by soil reduction with alterations in ionic species and their concentrations at clay surfaces and in soil solutions.  相似文献   

11.
R.J. Haynes  R.S. Swift 《Geoderma》1985,35(2):145-157
The effects of air-drying field-moist soils on the adsorption and desorption of added phosphate and on the levels of extractable native soil phosphate were examined using the A and B horizons of a group of four acid soils.Air-drying increased the capacity of all the soil samples to adsorb phosphate. At an equilibrium solution concentration of 0.5 μg P ml?1, the increase in the quantity of phosphate adsorbed following drying ranged from 23% to 70% of that adsorbed by the moist samples. Considerable hysteresis in phosphate adsorption—desorption isotherms was observed for both moist and dried soil samples indicating that the additional phosphate adsorbed by the dried samples was held with the same strength as that held by the moist samples.Air-drying the soil samples caused a small decrease in soil pH of approximately 0.1 pH unit and a general increase in levels of EDTA-extractable Fe, Al and organic matter. Quantities of native soil phosphate extractable with EDTA, resin and NaHCO3 were also increased. Concentrations of oxalate- and pyrophosphate-extractable Fe and Al and exchangeable Al were, however, unaffected by drying.It was also shown that when the phosphate content of NaHCO3 extracts is measured using the conventional molybdenum blue method, orthophosphate plus a differing amount of acid-hydrolysable organic P present in the extract is measured.  相似文献   

12.
Cadmium sorption was measured in 10 agricultural soils with pH ranging from 4.5 to 7.9, and total Cd content from 0.27 to 1.04 μg g?1 dry soil. With initial Cd concentrations of 0.5 to 100.0 μM, sorption from 0.002 M CaCl2 was described by the Freundlich adsorption equation but the gradients of the isotherms increased when the initial concentrations were below 0.5 μm. This indicates that there are specific sites of differing sorption energy; differences between soils in the gradients of the isotherms at low initial concentration could largely be accounted for by their contents of ‘free’ Fe2O3. When initial concentrations were below 0.5 μm there was a linear relationship between the quantity of Cd sorbed and the final concentration in solution. This relationship held with all soils except that of lowest pH from which there was a net loss of Cd to the solutions. Desorption was measured from three soils with contrasting pH. With the soil of lowest pH, over 80 per cent of sorbed Cd was desorbed to 0.002 m CaCl2 and up to 30 per cent to 100 or 500 μm solutions of heavy metal chlorides. In contrast, only very small proportions (<1.25 per cent) were desorbed from the other soils with pH 6.7 and 7.8. The results indicate that Cd is strongly sorbed by soils of pH of above 6.0 when added in amounts comparable to additions in sewage sludges or phosphatic fertilizers, and illustrate the importance of liming as a means of reducing the mobility of this metal in soils.  相似文献   

13.
Crop production on red soils in China is largely limited by the low availability of phosphorus, which is frequently attributed to the adsorption of phosphate by variable-charge minerals including Fe and Al oxides and kaolinite. Isotopic tracing analysis and soil incubation were carried out to investigate the desorption and microbial transformation of applied specifically sorbed P in two pH-contrasting light-textured soils. A rapid release of P from the added mineral-P surface complex in the two tested soils was observed. Most of the released P was recovered in a 0.5MNaHCO3 extract and in soil microbial biomass. Microbial biomass-32P was detected at early stages of incubation and reached up to 10–30% of the added 32P. Approximately 50–70% of the added complex 32P, varying between minerals and soils, was extractable in the 0.5MNaHCO3 at 75 days after incubation for the acid soil but up to 120 days for the neutral soil. Microbial biomass-P plus 0.5MNaHCO3-extractable 32P accounted for more than 60–80% of total added complex-32P, implying high desorption and transformation of the specifically sorbed P in the two soils. There was more inorganic 32P than organic 32P in the NaHCO3 extract, suggesting that chemical release of specifically sorbed P was dominant. Ligand exchange and chemical desorption due to a change in environmental conditions such as pH and ionic strength are likely the major mechanisms responsible for the chemical release of specifically sorbed 32P in the tested soils. Received: 29 September 1996  相似文献   

14.
Anaerobic reoxidation of reduced products in paddy soils was investigated. Ferrous iron (Fe2+) and monosulfide ion (S2–) added to the soil chemically reduced MnO2 to Mn2+, and MnO2 and Fe(OH)3 to Mn2+ and Fe2+, respectively, where Fe2+ and S2– were considered to be oxidized to Fe3+ and S0. Elemental sulfur was oxidized to sulfate by anaerobic incubation with NO3 MnO2 and Fe(OH)3. A new conceptual model for the reduction processes in submerged paddy soil including the reoxidation processes of reduced products, in which soil heterogeneity in paddy fields was taken into consideration, was proposed based on the results. Received: 20 October 1996  相似文献   

15.
P.M Huang  M.K Wang  M.H Wu  C.L Liu  T.S.C Wang 《Geoderma》1977,18(4):251-263
Twenty two surface soils, representing six parent materials and four soil groups, were sampled in Taiwan for the present study.Except in the soil derived from volcanic ash, the sesquioxidic components and relatively easily extractable Si were present only in small amounts in the NaOAc and H2O2- NaOAc extractable fractions. In addition to Fe, both Si and Al were present in the dithionite-citrate-bicarbonate extracts in considerable amounts, indicating that Si and Al were either present separately or in association with Fe in the sesquioxidic fractions of the soils. The amounts of Si, Al and Fe extracted by the dithionite-citrate-bicarbonate and boiling KOH treatments differed from sample to sample, indicating that they are important variables in the nature of the soils studied.The amounts of the ammonium oxalate-extractable Al and Fe, representing the noncrystalline sesquioxidic products of relatively recent weathering, also differed with parent materials and pedogenic processes. The statistical data indicate that the ammonium oxalate-extractable Al and Fe are related to the contents of organic matter but not to acidity and the contents of clay. The percentage distribution of the extractable Al in the > 2 μm fractions of the selected soil samples ranged from 22.0 to 52.5% and that of the extractable Fe from 11.1 to 38.1%, indicating that the active non-crystalline Al and Fe components in the non-clay fractions deserve close attention in the study of pedogenesis and other soil physicochemical reactions in relation to soil fertility and environmental protection.  相似文献   

16.
 The combined effects of soil compaction and soil waterlogging on the growth of two rice cultivars (Oryza sativa L., cultivars Kanto 168 and Koshihikari) and soil N transformations were studied in pots. Although waterlogging eliminated initial differences in mechanical resistance between compacted and loose soils, Kanto 168 and Koshihikari roots had, respectively, less biomass and a lower porosity if soil was compacted prior to waterlogging. The cause for this was probably established before waterlogging. Redox values showed that upland soils were well aerated. Loose waterlogged soils contained oxic sites, but compacted waterlogged soils did not. Potential denitrification was stimulated by waterlogging and, to a larger extent, by plant presence. Waterlogging lowered potential nitrifying capacities, by competition between plants and micro-organisms for NH4 + rather than by oxygen shortage. Compaction prior to waterlogging benefited the potential nitrifying capacity of soils with either cultivar and the potential denitrifying capacity for soils with Koshihikari. Compaction had no effect on nitrification or denitrification in upland soils. N recoveries were low, especially in pots without plants, as a result from sampling strategy and N loss. On day 42/43 after potting, total δ15N values of waterlogged pots were positive, whereas after 22 days all pots had negative total δ15N values. Final δ15N values of plant parts from waterlogged and upland soils were positive and negative, respectively. Although the δ15N values generally accorded well with the other results, they did not support higher N losses from compacted waterlogged soils than from loose waterlogged soils with plants, as suggested by potential denitrifying activities. Received: 4 February 2000  相似文献   

17.
This study investigated those soil factors related to iron (Fe) chlorosis between Fe status of peach leaves and some soil properties in the Antalya region of Turkey. The total Fe content of leaves was negatively correlated with soil pH and the organic matter content of the soils. Extractable Fe (by 1N HCl) was negatively correlated with the calcium carbonate (CaCO3) and bicarbonate (HCO3‐) content of the soils. In addition, both total‐ and extractable‐Fe contents of leaves were also negatively correlated with the copper (Cu) content of the soils. On the other hand, significant correlations were found among the Fe index, P/Fe ratio of leaves, and soil pH, phosphorus (P), zinc (Zn), and Cu content of the soils. It appears from these studies that high pH, and the CaCO3, HCO3‐, and Cu contents are effective soil factors affecting the availability of Fe and its uptake by the peach trees, and these soil factors were associated with severity of Fe chlorosis in the studied area.  相似文献   

18.
Phosphate sorption by calcareous soils has been studied mainly on heavily fertilized agricultural soils and soils with calcite as the main carbonate mineral. We examined factors affecting phosphate adsorption in the soils of a semi-arid, mediterranean, dolomitic, soil and vegetation chrono-sequence in southeastern Spain. The youngest soils are highly eroded, Sandy Regosols (Typic Xerorthents) under gorse-scrubland vegetation. These have small P sorption capacities, large Mg-Ca carbonate contents but small amounts of Fe and Al oxides. Small total P (HNO3/HClO4 digestion) concentrations (30–130 μg P g?1), of which up to 90% is Ca-bound (HCl-extractable), are typical of these young soils. P sorption markedly increased when Ca2+ was added to the solution. The fractionation of previously sorbed P indicates that the fate of most of this extra-sorbed P is the labile-P fraction sorbed on to (carbonate) surfaces and the apatite-like fraction (NaHCO3-extractable and HCl-extractable fractions). At the other extreme, older more-intensively weathered, sandy-clay-loam rendzinas (Entic Haploxerolls), supporting dense mature garrigue, have a much greater P adsorption capacity and larger clay and Fe and Al oxide concentrations. They have more total P (ca 400 μg P g?1), much of it in occluded form (residual fraction). These soils show no significant differences in P sorption whether or not CaCl2 was used as a background electrolyte. Considering the overall variations within the chronosequence, dithionite extractable Fe and Al are the properties best correlated with P sorption. This support the general finding that crystalline Fe-oxides (e.g. goethite and haematite) appear to be the most important P-sorbing component for soils in the Mediterranean region, rather than amorphous Fe-oxides (e.g. ferrihydrite) as is reported for more mesic areas. Stepwise multiple regression and fractionation data, however, suggest that, provided the soil solution is rich in Ca2+, carbonate may also be a significant contributing factor to P sorption, especially in the youngest of these dolomitic soils.  相似文献   

19.
TIME-DEPENDENT SORPTION OF PHOSPHATE BY SOILS AND HYDROUS FERRIC OXIDES   总被引:7,自引:0,他引:7  
The sorption of inorganic phosphate (P) by soils and hydrous ferric oxides was studied at times up to 192h. An initially rapid decrease in solution P concentration was followed by a much slower decrease between 48 and 192h with soils, Fe gel. and natural goethite, whereas synthetic goethite gave a well-defined equilibrium condition after only 48h. Resolution of the sorption isotherms showed that the increase in P sorption with time involved an appreciable shift of P from a more-physically sorbed form to a chemisorbed form. This was supported by chemical fractionation which showed that NaOH-extractable P was fairly constant with increasing sorption time, whereas the additional sorbed P was extracted by citrate-dithionite-bicarbonate from soils, and by HC1 from Fe gel and natural goethite. These sorbents contained short-range (amorphous) material, whereas synthetic goethite, from which all sorbed P was NaOH –extractable. did not. It is proposed that the time-dependent sorption of P and the associated shift of P to chemisorbed forms, involves the diffusion of P into “structurally porous”, short-range order material.  相似文献   

20.
Rice is the staple food crop for about 50% of the world's population. It is grown mainly under two ecosystems, known as upland and lowland. Lowland rice contributes about 76% of the global rice production. The anaerobic soil environment created by flood irrigation of lowland rice brings several chemical changes in the rice rhizosphere that may influence growth and development and consequently yield. The main changes that occur in flooded or waterlogged rice soils are decreases in oxidation–reduction or redox potential and increases in iron (Fe2+) and manganese (Mn2+) concentrations because of the reductions of Fe3+ to Fe2+ and Mn4+ to Mn2+. The pH of acidic soils increased and alkaline soils decreased because of flooding. Other results are the reduction of nitrate (NO3 ?) and nitrogen dioxide (NO2 ?) to dinitrogen (N2) and nitrous oxide (N2O); reduction of sulfate (SO4 2?) to sulfide (S2?); reduction of carbon dioxide (CO2) to methane (CH4); improvement in the concentration and availability of phosphorus (P), calcium (Ca), magnesium (Mg), Fe, Mn, molybdenum (Mo), and silicon (Si); and decrease in concentration and availability of zinc (Zn), copper (Cu), and sulfur (S). Uptake of nitrogen (N) may increase if properly managed or applied in the reduced soil layer. The chemical changes occur because of physical reactions between the soil and water and also because of biological activities of anaerobic microorganisms. The magnitude of these chemical changes is determined by soil type, soil organic-matter content, soil fertility, cultivars, and microbial activities. The exclusion of oxygen (O2) from the flooded soils is accompanied by an increase of other gases (CO2, CH4, and H2), produced largely through processes of microbial respiration. The knowledge of the chemistry of lowland rice soils is important for fertility management and maximizing rice yield. This review discusses physical, biological, and chemical changes in flooded or lowland rice soils.  相似文献   

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