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1.
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2.
Phosphorus (P) sorption processes in soils contribute to important problems in agriculture: a deficiency of this plant nutrient and eutrophication in aquatic systems. Soil organic matter (SOM) plays a major role in sorption processes, but its influence on P sorption remains unclear and needs to be elucidated to improve the ability to effectively manage soil P. The aim of this research was to investigate the influence of SOM on P sorption. The study was conducted in sandy soil profiles and in topsoils before and after removal of SOM with H2O2. The results were interpreted with the Langmuir and Freundlich isotherms. Our results indicated that SOM affected P sorption in sandy soils, but that P sorption also depended on specific soil properties (e.g. values of the degree of P saturation (DPS), P sorption capacity (PSC) and pH) often related to land use. Removal of SOM decreased PSC in most of the topsoils tested; other soil properties became important in controlling P sorption. An increase in P desorption observed after SOM removal indicated that SOM was potentially that soil constituent which increased P binding and limited P leaching from these sandy soils.  相似文献   

3.
王磊  孙成  郭会琴 《土壤》2012,44(3):366-373
土壤有机质(SOM)是土壤的重要组成部分,它对疏水性有机污染物(HOCs)的吸附作用对污染物在环境中的迁移转化有着至关重要的影响。近年来的一些研究表明,HOCs在SOM上的吸附行为并不严格地符合传统的线性分配模型。本文综述了近年来一些学者提出的SOM对HOCs的非线性吸附作用的机制及其影响因素,认为SOM的组成和结构均对HOCs的吸附有着重要的影响。SOM吸附在土壤矿物表面后,其结构或各组分的比例发生了改变,从而对其本身的吸附作用产生影响。溶液的化学环境(主要是阳离子)会对SOM的结构和吸附作用产生影响,特别是当溶液中存在一些过渡金属(如,铜或银)的离子时,共吸附的金属离子可能会与多环芳烃类分子形成阳离子-π键的作用,从而促进多环芳烃类物质在SOM上的吸附。  相似文献   

4.
Effects of soil organic matter (80M) on P sorption of soils still remain to be clarified because contradictory results have been reported in the literature. In the present study, pH-dependent P sorption on an allophanic Andisol and an alluvial soil was compared with that on hydrogen peroxide (H202)-treated, acid-oxalate (OX)-treated, and dithionite-citrate- bicarbonate (DCB)-treated soils. Removal of 80M increased or decreased P sorption depending on the equilibrium pH values and soil types. In the H2O2 OX-, and DCB-treated soils, P sorption was pH-dependent, but this trend was not conspicuous in the untreated soils. It is likely that 80M affects P sorption of soils through three factors, competitive sorption, inhibition of polymerization and crystallization of metals such as AI and Fe, and flexible structure of metal-80M complexes. As a result, the number of available sites for P sorption would remain relatively constant in the wide range of equilibrium pH values in the presence of 80M. The P sorption characteristics were analyzed at constant equilibrium pH values (4.0 to 7.0) using the Langmuir equation as a local isotherm. The maximum number of available sites for P sorption (Q max) was pH-dependent in the H202-, OX-, and DCBtreated soils, while this trend was not conspicuous in the untreated soils. Affinity constants related to binding strength (K) were less affected by the equilibrium pH values, soil types, and soil treatments, and were almost constant (log K ≈ 4.5). These findings support the hypothesis that 80M plays a role in keeping the number of available sites for P sorption relatively constant but does not affect the P sorption affinity. By estimating the Q max and K values as a function of equilibrium pH values, pH-dependent P sorption was well simulated with four or two adjustable parameters. This empirical model could be useful and convenient for a rough estimation of the pH-dependent P sorption of soils.  相似文献   

5.
This study investigated the effect of different farming practices over long time periods on the sorption‐desorption behavior of Cu, Cd, and Zn in soils. Various amendments in a long‐term field experiment over 44 y altered the chemical and physical properties of the soil. Adsorption isotherms obtained from batch sorption experiments with Cu, Cd, and Zn were well described by Freundlich equations for adsorption and desorption. The data showed that Cu was adsorbed in high amounts, followed by Zn and Cd. In most treatments, Cd ions were more weakly sorbed than Cu or Zn. Generally, adsorption coefficients KF increased among the investigated farming practices in the following order: sewage sludge ≤ fallow < inorganic fertilizer without N ≈ green manure < peat < Ca(NO3)2 < animal manure ≤ grassland/extensive pasture. The impact of different soil management on the sorption properties of agricultural soils for trace metals was quantified. Results demonstrated that the soil pH was the main factor controlling the behavior of heavy metals in soil altered through management. Furthermore, the constants KF and n of isotherms obtained from the experiments significantly correlated with the amount of solid and water‐soluble organic carbon (WSOC) in the soils. Higher soil pH and higher contents of soil organic carbon led to higher adsorption. Carboxyl and carbonyl groups as well as WSOC significantly influenced the sorption behavior of heavy metals in soils with similar mineral soil constituents.  相似文献   

6.
The effect of soil organic matter (SOM) on sorptive parameters under different soil management practices in Rendzic Leptosol was studied. In 2006, an experiment of different management practices in a productive vineyard was established in the locality of Nitra-Dra?ovce (Slovakia). The following treatments were established: (1) control (grass without fertilization), (2) T (tillage), (3) T + FYM (tillage + farmyard manure), (4) G + NPK3 (grass + 3rd intensity of fertilization for vineyards), (5) G + NPK1 (grass + 1st intensity of fertilization for vineyards). Soil samples were collected every month during the year 2010. Obtained results showed increased hydrolytic acidity (by 23%), sum of basic cations (by 37%) and decreased total cation exchange capacity (CEC) (by 36%) with higher doses of fertilization in comparison to control. Application of farmyard manure had a positive effect on the increase in the SOM cation sorption capacity. Positive correlations between pH and sum of basic cations (SBC) (r = 0.493, p ≤ 0.001), CEC (r = 0.498, p ≤ 0.001) and cation sorption capacity of SOM (r = 0.391, p ≤ 0.01) were observed. Higher values of labile carbon:potentially mineralizable nitrogen (CL:Npot) ratio corresponded with lesser CEC, SBC and base saturation values in the soil. With increased humus quality (higher values of humic acid:fulvic acid (CHA:CFA) ratio), cation sorption capacity of SOM significantly increased (r = 0.329, p ≤ 0.01). The results of this study proved that the application of farmyard manure had a positive effect on the increase of SOM sorption capacity, but higher doses of mineral fertilizers added to soil had a negative effect.  相似文献   

7.
Although the chemical composition of soil organic matter (SOM) is known to significantly influence sorption of pesticides and other pollutants, it has been difficult to determine the molecular nature of SOM in situ. Here, using 13C nuclear magnetic resonance (NMR) data and elemental composition in a molecular mixing model, we estimated the molecular components of SOM in 24 soils from various agro‐ecological regions. Substantial variations were revealed in the molecular nature of SOM. As a proportion of soil carbon the proportion of the carbonyl component ranged from 0.006 to 0.05, charcoal from 0 to 0.15, protein from 0.09 to 0.29, aliphatic from 0.14 to 0.30, carbohydrate from 0.21 to 0.31, and lignin from 0.05 to 0.42. The relationships between Koc (sorption per unit mass of organic carbon) of carbaryl (1‐naphthyl methylcarbamate) and phosalone (S‐6‐chloro‐2,3‐dihydro‐2‐oxobenzoxazol‐3‐ylmethyl O,O‐diethyl phosphorodithioate) and the molecular nature of organic matter in the soils were significant. Of the molecular components estimated, lignin and charcoal contents correlated best with sorption of carbaryl and phosalone. Aliphatic, carbohydrate and protein contents were found to be negatively correlated with the Koc of both pesticides. The study highlights the importance of the molecular nature of SOM in determining sorption affinities of non‐ionic pesticides and presents an indirect method for sorption estimation of pesticides.  相似文献   

8.
长期不同施肥红壤磷素特征和流失风险研究   总被引：11，自引：2，他引：11  
为探索长期施肥对红壤磷素吸附固持的影响,分析不同施肥土壤磷流失风险及影响因素。在南方丘陵区红壤上开展了持续25年的长期定位试验,处理包括:不施肥(CK)、施氮肥(N)、施磷肥(P)、施钾肥(K)、施氮磷钾肥(NPK1)、施2倍量氮磷钾肥(NPK2)、单施有机肥(OM)和氮磷钾配施有机肥(MNPK)。研究了不同施肥下土壤全磷、Olsen-P、Mehlich1-P、CaCl2-P含量及磷吸持指数(PSI)、磷饱和度(DPS)的变化,探讨不同施肥处理土壤对磷的吸附和解吸特征,并分析了土壤磷指标与土壤有机碳、pH、CEC之间的关系。结果表明:长期施用化学磷肥有利于补充土壤磷素,特别是土壤全磷,并使Olesn-P和Mehlich 1-P有增加趋势,而对CaCl2-P影响不显著;施用化肥对DPS影响不显著,单施磷会降低PSI,低量氮磷钾提高了PSI,高量氮磷钾处理与对照差异不显著;长期施用有机肥(猪粪)土壤全磷增加,而Olsen-P、Mehlich 1-P和CaCl2-P则大幅累积, PSI显著降低, DPS显著增加。长期施用化肥处理土壤对新添加磷的吸附较强,长期施用有机肥降低了土壤对新添加磷的吸附;土壤全磷、Olsen-P、Mehlich1-P、CaCl2-P、PSI、DPS及最大吸附容量(Qm)与土壤pH、CEC、土壤总有机碳(TSOC)、土壤水溶性有机碳[冷水提取水溶性有机碳(CWSOC)和热水提取水溶性有机碳(HWSOC)]间相关性较高;土壤磷指标和土壤有机碳、pH、CEC指标之间存在典型相关关系,第1对和第2对典型变量的典型相关系数分别为0.997和0.951,达显著水平。研究表明,施用有机肥是调节土壤磷的供给和保持的重要措施,土壤水溶性有机碳和pH可能是反映红壤磷素供应和流失的关键指标。  相似文献   

9.
活化过硫酸钠(Sodium persulfate,SPS)氧化技术是一种新型的土壤修复技术。为了更科学地评价化学氧化处理后土壤的环境风险,本文通过亚铁离子活化过硫酸钠法对有机质(Organic matter,OM)含量存在显著差别的两种土壤进行氧化处理,比较了活化过硫酸钠氧化前后两种土壤样品对3种挥发性有机污染物的吸附特性。结果表明,亚铁活化的SPS能够氧化土壤中腐殖酸和胡敏素类的有机质。对OM含量较高的1号土,SPS氧化对有机质的去除率为71.9%。而对OM含量较低的2号土,SPS氧化对有机质的去除率为49.9%。1号土样对3种挥发性有机物的吸附以分配作用为主,氧化后的1号土样对3种物质的吸附机制不变,但吸附量有所增加;2号土样对3种挥发性有机污染物的吸附有一定的非线性,而氧化后的2号土样对3种物质的吸附线性特征增强。吸附数据用对数形式的Freundlich方程拟合得到分配系数lg Kf值,比较有机碳标化后的分配系数lg Kfoc,氧化后的土壤有机质对3种挥发性有机污染物的吸附特性有所提高。分析表明,SPS氧化了有机质中较多的极性组分(如羧基及羟基等),从而使处理后的土壤中有机质的非极性增强,强化了对非极性化合物的吸附。  相似文献   

10.
Soil organic matter (SOM) plays an important role in the Se dynamics in soil. The potential effects of vermicompost and digestate as important sources of SOM on selenium (Se) mobility were assessed in this study. Three soils differing in their physicochemical parameters, fluvisol, chernozem, and luvisol, were chosen, and three types of vermicomposts based on various bio-waste materials as digestate (vermicompost 1), kitchen waste with woodchips (vermicompost 2), and garden bio-waste (vermicompost 3) were used due to their high organic matter content. Additionally, digestate samples alone were applied. To evaluate the potential effect of vermicompost application on sorption characteristics of soils, batch sorption experiments were performed. The results showed a predominant effect on Se species in the soils, where selenite sorbed more intensively compared to selenate, regardless of the soil and ameliorative material applied. In the control, the soil sorption ability of selenite tended to decrease in the order:fluvisol > luvisol > chernozem. However, these differences were not significant. Moreover, the effects of the ameliorative materials depended on both soil and amendment used. In fluvisol, all the amendment applications resulted in a decrease in distribution coefficient (Kd values) of Se, whereas in chernozem, this effect was observed only for the digestate-based vermicompost 1. Increasing Kd levels were reported in luvisol treated with digestate; the application of garden bio-waste-based vermicompost 3 tended to decrease the Kd values. Further studies are required on long-term effects of these amendments on Se mobility in soils and the role of individual organic matter fractions in this context.  相似文献   

11.
A comparative study was conducted on the toxicity of Cd to alkaline phosphatase activity (ALP) and dehydrogenase activity (DHA) in 18 top soils with contrasting soil properties representative of 14 major soil types in China. Soil pH and carbonate content, soil organic matter, and cation exchange capacity (CEC) largely affected the Cd toxicity on two enzyme activities; with the soil pH having only minor effect on the median ecological dose values based on total Cd concentrations (ED50 T). The values of ED50 T/ED50 W (based on water-soluble Cd content) of alkaline phosphatase and dehydrogenase were strongly influenced by pH and CEC contents, which explained up to 71% of the variation for alkaline phosphatase, 82% of the variation for dehydrogenase, and also were significantly correlated with the parameter KF derived from Freundlich adsorption isotherms. This study suggests that the values of ED50 T/ED50 W could be useful to evaluate the buffer capacity of soils which protects soil enzymes from harmful effects of heavy metal.  相似文献   

12.
Soil adsorption and the effect of four chlorophenols and three chloroanilines on the growth of lettuce (Lactuca sativa) were determined in two soil types differing in organic matter content and pH. Adsorption increased with increasing organic matter content of the soils. Phytotoxicity, based on dosed amounts, was significantly higher in the soil with the low level of organic matter. This difference could be reduced by recalculating the EC50 values for the effect of the test substances on plant growth in mg kg-1 dry soil towards concentrations in mg L-1 pore water using data from soil adsorption experiments. For pentachlorophenol only this recalculation increased rather than decreased the difference between the two soils, however, when the EC50 values for pentachlorophenol were corrected for the difference in soil pH, almost the same values resulted for both soils. Calculated EC50 values on the basis of pore water concentrations appeared to be in good agreement with values determined in nutrient solution tests. These results indicate that, for plants, the toxicity and therefore the bioavailability of organic chemicals in soil mainly depend on the concentration in the soil solution, and can be predicted on the basis of sorption data. Attempts to develop QSARs relating log EC50 values in μmol L?1 pore water with lipophilicity (expressed as the octanol/water partition coefficient: log Kow,) of the test substances resulted in a statistically significant relationship. This relationship was further improved by correcting the chlorophenol data for dissociation effects.  相似文献   

13.
The mobility of hydrophobic organic compounds (HOCs) in soils can be influenced by the presence of dissolved organic matter (DOM). While numerous studies have determined interactions of HOCs with humic and fulvic acids, only few data exist on the partitioning of HOCs to natural, non‐fractionated DOM as it occurs in soil solutions. In this study, DOM was extracted from 17 soil samples with a broad range of chemical and physical properties, originating from different land uses. The partition coefficients of pyrene to DOM were determined in all soil extracts and for two commercial humic acids using the fluorescence quenching method. For the soil extracts, log KDOC values ranged from 3.2 to 4.5 litres kg?1. For the Aldrich and Fluka humic acids, log KDOC was 4.98 and 4.96 litres kg?1, respectively, thus indicating that they are not representative for soil DOM. After excluding these two values, the statistical analysis of the data showed a significant negative correlation between log KDOC and pH. This was also shown for one sample where the pH was adjusted to values ranging from 3 to 9. A multiple regression analysis suggested that ultraviolet absorbance at 280 nm (an indicator for aromaticity) and the E4:E6 ratio (an indicator for molecular weight) had additional effects on log KDOC. The results indicate that the partitioning of pyrene to DOM is reduced at alkaline pH, probably due to the increased polarity of the organic macromolecules resulting from the deprotonation of functional groups. Only within a narrow pH range was the KDOC of pyrene mainly related to the aromaticity of DOM.  相似文献   

14.
Microbial biomass, respiratory activity, and in‐situ substrate decomposition were studied in soils from humid temperate forest ecosystems in SW Germany. The sites cover a wide range of abiotic soil and climatic properties. Microbial biomass and respiration were related to both soil dry mass in individual horizons and to the soil volume in the top 25 cm. Soil microbial properties covered the following ranges: soil microbial biomass: 20 µg C g–1–8.3 mg C g–1 and 14–249 g C m–2, respectively; microbial C–to–total organic C ratio: 0.1%–3.6%; soil respiration: 109–963 mg CO2‐C m–2 h–1; metabolic quotient (qCO2): 1.4–14.7 mg C (g Cmic)–1 h–1; daily in‐situ substrate decomposition rate: 0.17%–2.3%. The main abiotic properties affecting concentrations of microbial biomass differed between forest‐floor/organic horizons and mineral horizons. Whereas microbial biomass decreased with increasing soil moisture and altitude in the forest‐floor/organic horizons, it increased with increasing Ntot content and pH value in the mineral horizons. Quantities of microbial biomass in forest soils appear to be mainly controlled by the quality of the soil organic matter (SOM), i.e., by its C : N ratio, the quantity of Ntot, the soil pH, and also showed an optimum relationship with increasing soil moisture conditions. The ratio of Cmic to Corg was a good indicator of SOM quality. The quality of the SOM (C : N ratio) and soil pH appear to be crucial for the incorporation of C into microbial tissue. The data and functional relations between microbial and abiotic variables from this study provide the basis for a valuation scheme for the function of soils to serve as a habitat for microorganisms.  相似文献   

15.
为评价宁南山区草地植被不同恢复方式对土壤入渗性能的影响,以不同植被群落的饱和导水率为研究对象,采用逐步回归研究退耕农地、禁牧荒地、封育草地导水率的变化及影响因子,并探讨了其作用机制。结果表明：3种植被恢复方式均有利于0-40 cm土壤饱和导水性能提高;各土层土壤饱和导水率均随植被恢复而不断提高,0-5 cm土层改善作用最为明显;农地退耕序列和荒地禁牧序列5-40 cm土层、封育草地序列0-40 cm土层土壤饱和导水率随土层深度下降而降低;影响土壤饱和导水率的因子为土壤有机质因子和土壤结构因子;3种植被恢复方式土壤有机质质量分数与Ks均呈显著的线性相关关系,在该区域有机质质量分数越高,Ks增加越快;土壤有机质积累是土壤饱和导水率提高的根本动力。因此,草地封育更利于提高使该地区土壤导水性能提高,促进生态恢复。  相似文献   

16.
通过往土壤中添加不同量小麦秸秆,经好气培养1年后,获得不同有机质含量梯度的系列土壤,研究有机质含量对石灰性黄潮土和砂姜黑土磷（P）相关吸附参数和不同水土比下解吸溶液P浓度的影响。结果表明,Langmuir方程能够较好地拟合不同有机质含量的两种土壤对P的等温吸附曲线,拟合度均达到显著（P 0.05）或极显著（P 0.01）水平。黄潮土和砂姜黑土P最大吸附量（Xm）、吸附结合能常数（K）、最大缓冲容量（MBC）、吸附饱和度（DPS）及相同水土比下P解吸溶液浓度与有机碳含量间均呈显著或极显著的二次抛物线关系。抛物线拐点之前,随有机质含量的提高,P的吸附能力增强,解吸能力降低;拐点之后,吸附能力降低,解吸能力增强。各水土比条件下,P解吸溶液浓度与Xm、K、MBC呈显著或极显著负相关,与DPS呈显著或极显著正相关。随有机质含量的提高,土壤P植物有效性和P流失风险呈先降低后增强的抛物线趋势;土壤供P缓冲能力则先增强后降低。砂姜黑土Xm、K、MBC均明显高于黄潮土,DPS明显低于黄潮土;且其抛物线拐点滞后,拐点横坐标有机碳含量明显高于黄潮土。不同有机质含量的解吸曲线较黄潮土排列紧密;砂姜黑土黏粒含量、碳酸钙含量明显高于黄潮土,全P和Olsen-P含量明显低于黄潮土,这可能是影响两种石灰性土壤P吸附–解吸特性差别的主要原因。  相似文献   

17.
The objective of this study was to investigate the effects of mono‐ and polyvalent cations on sorption of the two hydrophobic compounds nonylphenol (NP) and phenanthrene (Phe). To this end, exchange sites of a sandy soil were saturated with either Na+, Ca2+, or Al3+ and excess salts were removed by washing. The samples were then sterilized and either stored moist, dried at room temperature, or at 20°C, 60°C, or 105°C in a vented oven. Saturation with Na+ led to an increase of dissolved organic C (DOC) concentration in the soil water extracts, whereas the polyvalent cations Ca2+ and Al3+ decreased it. The 1H‐NMR relaxometry analyses showed that Al3+ restricted the mobility of water molecules that are confined within the SOM structure to a higher extent than Ca2+ or Na+. According to contact‐angle (CA) analyses, cation treatment did not significantly change the wetting properties of the samples. Batch sorption–desorption experiments showed no clear salt‐treatment effects on the sorption and desorption equilibria or kinetics of NP and Phe. Instead, the sorption coefficients and sorption hysteresis of NP and Phe increased in dry soil. With increasing drying temperature the CA of the soils and the sorption of both xenobiotics increased significantly. We conclude that structural modifications of SOM due to incorporation of polyvalent cations into the interphase structure do not modify the sorption characteristics of the soil for hydrophobic compounds. Instead, increasing hydrophobization of organic soil constituents due to heat treatment significantly increased the accessible sorption sites for nonpolar organic compounds in this soil.  相似文献   

18.
Understanding the role of organic acids on phosphorus (P) sorption capacity of soils is very important for its economic and friendly management. Combining P application with low-molecular weight organic acids could result in its higher plant availability for prolonged time. Therefore, citric and oxalic acid (at the rate of 1.0 mM kg?1 soil) were evaluated for their effect on P sorption capacity and its plant availability in two different textured calcareous soils. Organic acids decreased P sorption capacity and organic carbon partition coefficient (Koc) whereas increased Gibbs free energy (ΔG) of P. Organic-acid-treated soils required lesser quantity of P fertilizer to produce soil solution P concentration optimum for plant growth (external P requirement [EPR0.2]), that is, 0.2 mg L?1. Citric acid was efficient than oxalic acid in the above effects. P sorption parameters of Freundlich model were negatively correlated with lime potential and ΔG whereas had positive correlation (P < 0.05) with EPR0.2 and Koc. Incubation with oxalic acid increased available P in loamy sand and loam soil by 20% and 30%, respectively. Thus, organic acids could help reduce application rate of P fertilizer through lowering its adsorption in highly P-fixing soils without compromise on yield.  相似文献   

19.
Relationships between soil lightness, soil organic matter (SOM) composition, content of organic C, CaCO3, and texture were studied using 42 top‐soil horizons from different soil types located in southern Germany. SOM composition was determined by CPMAS 13C NMR spectroscopy, soil color was measured by diffuse‐reflectance spectrophotometry and given in the CIE L*a*b* color coordination system (Commission Internationale de l'Eclairage, 1978). Multiple‐regression analysis showed, that soil lightness of top‐soil horizons is principally determined by OC concentration, but CaCO3 and soil texture are also major variables. Soil lightness decreased with increasing OC content. Carbonate content had an important effect on soil lightness even at low concentrations due to its lightening property. Regressions between soil lightness and organic C content were strongly linear, when the soils were differentiated according to texture and CaCO3 content. The aryl‐C content was the only SOM component which correlated significantly with soil lightness (rS = –0.87). In the linear regressions carried out on the different soil groups, soil aryl‐C content was a more significant predictor for soil lightness than total OC content.  相似文献   

20.
土壤组分对广东省酸性水稻土磷吸附参数的影响   总被引：9，自引：2，他引：7  
Soil components affecting phosphate sorption parameters were studied using acid paddy soils derived from basalt, granite, sand-shale and the Pearl River Delta sediments, respectively, in Guangdong Province.For each soil, seven 2.50 g subsamples were equilibrated with 50 mL 0.02 mol L-1 (pH=7.0) of KCl containing 0, 5, 10, 15, 25, 50 and 100 ng P kg-1, respectively, in order to derive P sorption parameters (P sorption maximum, P sorption intensity factor and maximum buffer capacity) by Langmuir isotherm equation. It was shown that the main soil components influencing phosphate sorption maximum (Xm) included soil clay, pH,amorphous iron oxide (Feo) and amorphous aluminum oxide (Alo), with their effects in the order of Alo ＞Feo ＞ pH ＞ clay. Among these components, pH had a negative effect, and the others had a positive effect.Organic matter (OM) was the only soil component influencing P sorption intensity factor (K). The main components influencing maximum phosphate buffer capacity (MBC) consisted of soil clay, OM, pH, Feo and Alo, with their effects in the order of Alo ＞ OM ＞ pH ＞ Feo ＞ clay. Path analysis indicated that among the components with positive effects on maximum phosphate buffer capacity (MBC), the effect was in the order of Alo ＞ Feo ＞ Clay, while among the components with negative effects, OM ＞ pH. OM played an important role in mobilizing phosphate in acid paddy soils mainly through decreasing the sorption intensity of phosphate by soil particles.  相似文献   

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