评价土壤磷素植物有效性的物理化学指标

室内分析结合温室盆栽试验研究了土壤磷素植物有效性和无机磷酸盐的解吸特性之间的关系。供试材料为浙江省分布较广的四种代表性土壤,并以吸磷能力较强的黑麦为指示植物。结果表明,在四种供试土壤上黑麦吸收磷与解吸磷之间的相关性都比与两种常规化学方法浸提磷之间的相关性更为显著。不仅如此,黑麦吸收磷与解吸磷间在数量上较化学浸提磷要接近的多,并且在各供磷强度下以及不同土壤上都符合较好。黑麦吸收磷或解吸磷(Q)随土壤供磷强度(I)变化的Q—I关系能够很好地符合Langmuir方程;而Olsen-P和Brayl-P对供磷强度的关系与该方程的符合性在酸性土壤上要差得多。可见,植物吸收磷与磷酸盐解吸有内在联系。结果还表明,由拟合Langmuir方程计算得的最大解吸缓冲容量(MBCD)能够很好解释不同性质土壤间磷肥利用率的差异,它较之最大吸附缓冲容量(MBCA)能够更好指示土壤中磷的植物有效性。但平衡解吸缓冲容量反映土壤供磷能力更为灵敏,可望成为好的土壤磷诊断指标。     

Change Point in Phosphorus Release from Variously Managed Soils with Contrasting Properties

Abstract

Investigating the relation between concentration or release of phosphorus (P) into soil solution (CaCl₂‐P, determined by 0.01 M CaCl₂ extraction of soils) and soil test phosphorus (Olsen P, or 0.5 N NaHCO₃‐extractable soil phosphorus) for 10 widely ranging and variously managed soils from central Italy, a change point was evident where the slopes of two linear relationships meet. In other words, it was possible to distinguish two sections of the plots of CaCl₂‐P against Olsen P, for which increases of CaCl₂‐P per unit of soil test P increase were significantly (p<0.05) greater above than below these change points. Values of change point ranged from 14.8 to 253.1 mg kg^?1 Olsen P and were very closely correlated (p<0.001) to phosphorus sorption capacity of soils. Similar change points were also previously observed when Olsen P (and also Mehlich 3 P) of surface soils was related to the P concentration of surface runoff and subsurface drainage. Because insufficient data are available relating P in surface soils and amount of P loss by overland, subsurface, or drainage flow, using the CaCl₂ extraction of soil can be convenient to determine a change point in soil test P, which may be used in support of agricultural and environmental P management.     

Phosphorus sorption isotherm characteristics and availability parameters of Appalachian acidic soils

Abstract

Phosphate (P) sorption isotherms have been widely used to characterize the P status and to establish fertilizer requirements of soils. Recently, mechanistic models have successfully described the nutrient uptake by plants under changing soil and plant parameters. Phosphorus sorption characteristics of eleven representative soils of the Appalachian Region of the United States were evaluated, and experimental P adsorption data were fitted to Temkin, Freundlich, and Langmuir equations to determine the relative importance of the soil parameters in P retention and supply to plant roots. The Barber and Cushman model was used to predict the effect of P fertilization on P uptake by plant. The soils of Appalachia differ considerably with respect to the retention of added P. All three isotherm equations gave good fit with the experimental data and were reliable to describe the P quantity/ intensity relationships of these soils. The following sequence of P adsorption capacity in various soils was established: Tate (BA)? Hayesville (Bt) > Westmoreland (Bt2) ～ Upshur (Btl) ～ Gilpin (A) > Lily (A) ～ Dandridge (E) ～ Watauga (Ap) > Ashe (A) ～ Berks (A) ～ Dekalb (A). In spite of the great differences among soil properties related to surface area and degree of weathering of these soils, the content of free iron (Fe) oxides was the only soil property that correlated with the constants of the isotherm equations. Amounts of P required to give 0.20 μg P/mL varied with soils and were closely related to the constants of the isotherm equations. Soil P parameters from the P adsorption isotherms were used to determine a measure of Cli, b, and De instead of those used conventionally in the Barber and Cushman (1981) model to predict P uptake by corn. Predicted P uptake by corn varied with soils, even at the same P concentration in equilibrium solution (0.20 μg P/mL) or when an equal amount (90 μg P/mL) of P was added to all soils. Predictions of P uptake, however, were not correlated with the amount of P required to give 0.20 μg P/mL in 0.01M CaCl₂ solution or with the constants of the isotherm equations used. Diffusion coefficient and equilibrium P concentration in solution, and two intensity factors, were more important than buffer power in predicting P supplied to roots. These findings may help to explain the lack of significant correlations between the constants of the P isotherm equations and P uptake.     

长期不同施肥红壤磷素特征和流失风险研究

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。     

Sorption of phosphorus in field-moist and air-dried samples from four weakly developed cultivated soil profiles

Sorption of phosphorus (P) in complete soil profiles in northern Europe is not adequately documented. I measured the sorption in genetic horizons of four cultivated soils (Inceptisols, Spodosol) in Finland using both field‐moist and air‐dried soil samples, fitted modified Freundlich equations (Q = a × I^b ? q) to the data, and presented the results in quantity/intensity (Q/I) graphs. Least‐squares‐estimates for the parameters of the modified Freundlich equation (a, b, q) were found to be imprecise measures of sorption. Values derived from the fitted equations (the amount of P sorbed at the P concentration of 2 mg litre^?1 and P buffering capacity at the same concentration) were more precise. Both were correlated with concentrations of oxalate‐extractable iron and aluminium. In all soils, there was a distinct difference in sorption between the fertilized Ap horizons and the subsurface horizons, which retained P strongly. Most of the sorption capacity was located in the B horizons at depths between 0.3 and 0.7 m. The results demonstrate the effects of soil‐forming processes and human impact on the sorption of P in the soils. Drying the samples prior to the sorption experiments altered the shape of the Q/I graphs. It increased dissolution of P at small P concentrations, sorption at large P concentrations, and the estimates for P buffering capacity. The effects of drying soil samples on the results and the imprecision of the parameters estimated with the modified Freundlich equation should be taken into account when interpreting results of Q/I experiments.     

The effect of previous P additions on sorption indices of calcareous soils determined with commonly employed methods

The effect of previous P additions on commonly used sorption parameters was studied using four alkaline-calcareous soils of Greece, two Vertisols and two Entisols. Solution concentration and buffering capacity indices were significantly affected while sorption curves of the quantity of P removed from the solution (x/m) against final P solution concentration (c) were shifted to the right, towards the higher c concentration values. Different buffering indices (e.g. the slope of the Freundlich equation, the slope of the semi-logarithmic sorption curve of x/m against log c, the slope of the linear portion of the high c concentration range) showed an increasing trend with increasing previous P additions to the soils, with the exception of the slope of the tangent of the Freundlich equation at c = 1 μg P/ml. However, correction for the quantity of exchangeable P already present in the soil (q), resulted in an increasing trend for this parameter as well, while obviously it did not have any effect on the slopes of the linear portions of the sorption curves. Chemical changes, as for example the slow formation of insoluble Ca–P salts, could possibly explain the increased capacity of previously fertilized alkaline-calcareous soils to remove P from the experimental equilibration solution suggested by the increasing trend in the buffering indices of the present work. At any case, this effect should be taken into account, especially in studies where sorption parameters are related to various soil-plant characteristics with respect to P.     

上海土壤磷的吸附特性及缓冲性能的研究

本文以上海土壤为对象,研究选定了土壤磷等温吸附试验条件为:水土比10,平衡时间6天,控温25℃,磷加入量为100,200,400,600μgP/g土,溶液基质为0.01M CaCl₂。磷缓冲能力试验条件为:平衡时间2天,磷加入量为20,40,100,200μgP/g土。根据Freundlich, Tempkin和Langmuir方程计算的土壤吸附指标与土壤类型及土壤性质有密切关系,是土壤磷素肥力的重要指标。反映土壤缓冲能力的“磷肥指标”与土壤有机质、粘粒、活性铝及pH值相关较好。上海几种主要土壤中以青紫泥的最大吸附量(X_m),0.2ppm P吸附量和“磷肥指标”为最高,其次为青黄土,沟干泥和黄泥头,最小为夹沙泥。应用磷吸附指标与“磷肥指标”来预测土壤需磷量,初步试验是可行的,但实际应用还需进一步试验研究。     

长期轮作与施肥对农田土壤磷素形态和吸持特性的影响

通过对黄土旱塬地区长期定位施肥(26a)条件下的不同轮作系统的土壤磷素形态和吸持参数的测定,研究了轮作和施肥对土壤磷素吸持特性和磷素形态的影响,以及土壤磷素吸持参数与磷素形态之间的关系。结果表明,长期轮作与施肥都可以减低土壤磷素的最大吸附量（Qm）,相对于其它轮作和连作,在氮磷（NP）施肥下,小麦-玉米-豌豆轮作可以减低土壤的Qm,在氮磷有机肥（NPM）施肥下,小麦-玉米轮作可以减低土壤的Qm。在施肥相同的条件下,小麦-玉米轮作和小麦-豌豆轮作可以显著增加土壤中各形态无机磷的含量,长期轮作比连作可以增加土壤中的有效磷养分,尤其对Ca2-P的提高效果更为显著。相关分析表明,Qm和磷吸持指数（PSI）与全磷（T-P）、Olsen-P、CaCl2-P、Ca2-P、Ca8-P、Fe-P、Ca10-P和有机磷呈极显著负相关（p＜0.01）,与闭蓄态磷（O-P）呈显著负相关（p＜0.05）,与Al-P关系不显著。土壤有机质（SOM）与Qm、PSI和磷最大缓冲能力（MBC）之间存在极显著负相关关系,与磷吸持饱和度（DPSS）存在显著正相关。通径系数和逐步回归分析表明,在石灰性黑垆土土壤的无机磷形态中,Ca2-P对Olsen-P的贡献最大。     

Development of an alternative to the Olsen bicarbonate-extraction test for determining plant-available phosphorus in basaltic soils

Abstract. Recent work has demonstrated that the Olsen test for phosphorus (P) is an unreliable predictor of plant-available P in soils derived from basalt parent material in Northern Ireland. The present study was conducted to develop a more reliable soil-P test for these soils by regressing P fractions removed from soil by various chemical extractants against herbage P indices calculated from plant tissue test data using a diagnosis and recommendation integrated system. The degree of P saturation of the soil P sorption capacity, based on ammonium oxalate extractable P, Al and Fe, provided a better prediction of P available to swards on basaltic soils than either the Olsen test or a number of other well-known soil-P test procedures. The superiority of the degree of P saturation test on basaltic soils was attributed to the fact that it simultaneously takes account of both P quantity and P buffering capacity factors in predicting P availability. The Olsen-P test, which accounts for the P quantity factor alone, was only reliable for non-basaltic soils. Re-classifying the P fertility status of basaltic soils according to the degree of P saturation test could result in considerably less P being recommended for these soils with possible consequential benefits to water quality.     

冬小麦–夏休闲体系作物产量和土壤磷形态对长期施肥的响应

【目的】 研究土壤无机磷和有机磷组分变化,有助于选择和优化特定作物体系下不同肥料管理措施,提高磷资源效率。 【方法】 基于20年土冬小麦/夏休闲体系长期肥料定位试验,利用Tiessen-Moir磷素分级法,测定土壤无机磷和有机磷组分,并分析其与小麦磷吸收量、土壤磷表现平衡之间的关系。试验设7个处理:不施肥 (CK)、单施化学氮肥 (N)、氮钾化肥配施 (NK)、磷钾化肥配施 (PK)、氮磷化肥配施 (NP)、氮磷钾化肥配施 (NPK) 和氮磷钾化肥配施有机肥 (MNPK)。 【结果】 旱作条件下,20年长期NP、NPK和MNPK处理较CK、N、NK、PK处理显著提高了小麦籽粒产量,年平均增产在205～265 kg/hm2之间,以MNPK增幅最高。NP、NPK和MNPK处理较CK处理显著提高了小麦籽粒和秸秆吸磷量。PK、NP、NPK、MNPK处理较CK处理显著提高了树脂磷 (Resin-P)、碳酸氢钠提取无机磷 (NaHCO₃-Pi)、氢氧化钠提取无机磷 (NaOH-Pi)、浓盐酸提取无机磷 (C.HCl-Pi) 和残余磷 (Residual-P) 含量,显著降低了碳酸氢钠提取有机磷 (NaHCO₃-Po) 和氢氧化钠提取有机磷 (NaOH-Po) 含量。PK、NP、NPK与CK相比,对稀盐酸提取无机磷 (D.HCl-Pi)、浓盐酸提取有机磷 (C. HCl-Po) 含量影响不大,而MNPK显著提高了D. HCl-Pi和C. HCl-Po含量。N、NK处理较CK显著增加了Residual-P和C. HCl-Po,显著降低了NaHCO₃-Po和NaOH-Po,对Resin-P、NaHCO₃-Pi、NaOH-Pi、C.HCl-Pi和D.HCl-Pi含量没有影响。与试验初始时相比,长期施用化学磷肥和有机肥主要增加了土壤中可利用态无机磷的比例,降低了残余态磷和有机磷的比例。土壤中Resin-P、NaHCO₃-Pi和C. HCl-Pi与小麦磷吸收量之间呈显著正相关关系。磷素盈余显著增加了D. HCl-Pi、Resin-P和NaHCO₃-Pi的含量。 【结论】 供试土壤条件下,NP、NPK和MNPK三种平衡施肥措施都不仅有利于作物增产,而且有利于保持高比例的土壤有效磷库。      

Phosphate sorption by red mediterranean soils from Greece

Abstract

In nineteen surface horizons of red Mediterranean soils from various locations of Greece, phosphorus (P) sorption experiments were conducted and the sorption characteristics were studied in relation to soil properties. Phosphate sorption data were fitted both to the Langmuir and Freundlich equations. From these equations, the following P sorption parameters were determined from the Freundlich equation, X = ACⁿ, the parameters A (the phosphate sorbed at C = 1 mg P/L), n (the P sorption intensity), the P sorption index (PS = X/log C) and maximum P sorption (Xmfr). From the Langmuir equation, C/X = 1/KXm + C/Xm, the parameters K (showing the bonding energy), maximum P sorption (Xmla), the quantity of P adsorbed at a standard concentration of 0.2 mg P/L (P0.2), and P maximum buffering capacity (PMBC). The Freundlich parameter A was strongly correlated to the clay and sesquioxides ("free”; iron and aluminum oxides and amorphous iron oxides) content. Seventy‐four percent of the variance of this parameter was explained by clay and “free”; iron (Fe) content. The Freundlich parameter n was significantly correlated with pH and amorphous iron oxides content, while 52% of its variance was explained by amorphous Fe and dithionite extrac‐table aluminum (Al). The P sorption maxima calculated from the Freundlich equation were in general lower than those calculated by the Langmuir equation. Both these parameters were strongly correlated with clay and more slightly with sesquioxides content. About 50% of their variance was explained by clay content of the soils. The P sorption index was strongly correlated with the clay content and less strongly with dithionite‐extractable Fe and Al. The P‐buffering capacity calculated from the data of Langmuir equation was also strongly correlated with these two parameters. In addition, clay content and dithionite‐extractable Fe and Al were well correlated to the amounts of P required to obtain an equilibrium concentration of 0.2 mg P/L while 61% of the variation of this parameter was explained by the clay and the dithionite‐extractable Fe content. From these findings, it seems that for the red Mediterranean soils from Greece, P sorption is affected by clay content and iron and aluminum oxide contents.     

Distribution of Inorganic and Organic Phosphorus Fractions in Two Phosphorus-Deficient Soils as Affected by Crop Species and Nitrogen Applications

It is desirable to know the distribution of phosphorus (P) fractions in soil so that plants may use P efficiently. Here we report the dynamics of inorganic and organic P in P-deficient black and rice soil cropped by soybean, white lupin, and maize supplied with nitrogen (N) inputs by N fixation and urea fertilizer. Inorganic P fractions of the three cropped soils could be ranked as O-P (organic phosphorus) > Al-P (aluminum phosphorus) > Fe-P (iron phosphorus) > Ca₁₀-P (calcium-10 phosphorus) > Ca₈-P (calcium-8 phosphorus) > Ca₂-P (calcium-2 phosphorus), irrespective of soil type. The potential of various inorganic P fractions to plant nutrition differed between soybean and white lupin. The percentage of total P present as inorganic P was affected by crop, soil type, and N source. In black soil, the change of organic P fraction induced by N fixation was larger than by urea application. The moderately labile organic P (MLOP) concentration was not affected significantly by soil type and crop species, and it was probably the main P source to the inorganic P fraction because the correlation between the two pools was high (r = 0.945; P < 0.05). Crop species differed in their uptake of inorganic and organic P from soil. Though P fraction concentrations varied between black soil and rice soil, their response to crop species and N source was similar. The amounts of P removed from soil were affected by N source. The right choice of crop species and the application a suitable N source may increase crop yield and P uptake by plant in P-deficient soils.     

Assessing the Feasibility of Olsen P and P Sorption Parameters in Acidic Soils

Plant-available phosphorus (P) and P adsorption capacities are important for crop growth in acidic soils. Olsen P test, which is based on extraction with bicarbonate for predicting the amount of soil P available to plants, was used in this work. Soil P-adsorption capacities were determined by Langmuir line equation. The purpose of this work was to examine the suitability of Olsen P for predicting phytoavailable P and P sorption parameters in acid soil. To this end, we (i) assessed the phytoavailable P by successively pot-cropping rice and (ii) P adsorption characteristics of soil and their relation with Olsen P. Plant-available P, estimated by Olsen P in tested soil, was correlated to labile P. Qm (phosphorus sorption maximum) was negatively correlated with K (P sorption strength). P buffering capacity of soils was P3 (the highest P rate) >P2 (the second highest P rate) >P1 (the lowest P rate) >P0 (no P adding) after 75 day’s rice growth, which indicated P replenishment capacity was different among P treatments. This also suggested that P of plant uptake may decrease soil buffering capacity, especially for soils that contained relatively lower amounts of P. Qm and K were not significantly correlated to Olsen P. Degree of P saturation and Olsen P shared the similar trend with the change of P application rates and sampling dates. We concluded P status in soil can be characterized by degree of P saturation and Olsen P in tested soil. They were able to explain P status from both agronomic and environmental aspects.

Abbreviations: Qm, P sorption maximum; K, P sorption strength; P3, highest P rate in soil; P2, second highest P rate in soil; P1, lowest P rate in soil; P0, P adding in soil.     

Phosphorus Adsorption Isotherm: A Key Aspect for Effective Use and Environmentally Friendly Management of Phosphorus Fertilizers in Calcareous Soils

Crop response to the phosphorus (P) application is often erratic in most soil types in the world. In Algeria, there is no information on the P behavior in calcareous soils. The purposes of this work were to investigate the degree of P fixing capacity and to predict P fertilizer requirements of crops according to calcareous levels in the soil. Soil samples (at 0–30 cm depth) were collected and spiked with 0, 25 and 50% of lime (CaCO₃). Phosphate sorption curves were well fitted to the Freundlich equation. Results indicated that the calcareous level was predominantly controlled the P sorption indices [sorption capacity (a), and P sorption energy (n)] to affect the estimation of external d P requirement (EPR_0.2) and P fertilizer rates. The understanding of P sorption and desorption by soils and extrapolating the developed relationship between soil calcareous contents and P fertilizer rates would be quite promising and accurate approach for the economic and effective use of P fertilizers in calcareous soils of Algeria.     

Use of adsorption and buffer capacity in soil testing for phosphorus

Abstract

The methods used to predict phosphorus (P) fertilizer requirements use extractable P levels. The inclusion of soil P buffer capacity with extractable P levels to improve fertilizer P prediction accuracy should be further investigated for Mediterranean soils. The objectives of this study, were to characterize the P adsorption properties of selected soils and to compare different soil P buffering capacity indices to determine their contribution to predict P fertilizer requirement. Twenty‐one soils were collected and P adsorption isotherms determined. On 11 soils wheat was grown in the greenhouse and P requirement determined. The Langmuir adsorption isotherm described the P adsorption of all soils. The prediction of crop P requirement was improved by the inclusion of a soil P buffer capacity index in the prediction equation. The index proposed by Salmon is easy to determine under routine soil analyses and does not require special analytical equipment. However, clay content can be used to predict the Salmon buffer index for similar soils.     

Impact of Soil Sorption Characteristics and Bedrock Composition on Phosphorus Concentrations in two Bohemian Forest Lakes

Phosphate (PO₄-P) sorption characteristics of soils and bedrock composition were determined in catchments of two mountain lakes, Ple?né Lake (PL) and ?ertovo Lake (CT), situated in the Bohemian Forest (Czech Republic). The aim was to explain higher terrestrial P export to mesotrophic PL compared to oligotrophic CT. Concentrations of Al and Fe oxides were the dominant parameters affecting soil ability to adsorb PO₄-P. Depending on concentrations of Al and Fe oxides, P sorption maxima varied from 9.7 to 70.5 mmol kg^?1 and from 7.4 to 121 mmol kg^?1 in organic and mineral soil horizons, respectively. The catchment weighted mean PO₄-P sorption capacity was 3.4 mol m^?2 and 11.9 mol m^?2 in the PL and CT soils, respectively. The higher PO₄-P sorption capacity in the CT catchment was predominantly associated with higher pools of soil and Fe oxides. The CT bedrock (mica schist) released one order of magnitude less P than the PL bedrock (granite) within a pH range of catchment soils (pH_CaCl2 of 2.5–4.5). The higher ability of PL bedrock to release P and the lower ability of PL soils to adsorb PO₄-P thus contributed to the higher terrestrial P loading of this lake.     

氧化还原条件对土壤磷素固定与释放的影响

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。     

磷肥和有机肥对不同磷水平土壤磷吸附-解吸的影响

采用培养试验结合Langmuir吸附等温方程进行拟合求出吸附、解吸的相关参数的方法,研究了磷肥和有机肥对不同磷水平土壤磷吸附和解吸特性的影响。结果表明,随土壤磷水平和磷肥和有机肥用量的增加,土壤最大吸磷量、土壤磷最大缓冲能力显著降低;土壤易解吸磷和土壤磷的解吸率显著增加。土壤易解吸磷和土壤磷的解吸率与土壤Olsen-P呈显著正相关;土壤最大吸磷量、土壤磷最大缓冲容量与土壤Olsen-P呈显著负相关。单位量磷肥所增加的土壤易解吸磷随着磷肥用量和土壤磷水平的增加而增大;土壤磷水平和磷用量是影响土壤磷最大吸磷量和土壤磷最大缓冲能力的重要因素。     

长期施磷对土壤磷素吸附演变的影响

Knowledge of phosphorus （P） behavior in long-term fertilized soils is essential for programming fertilization practices and for sustaining environmental quality. The long-term （1984-1997） effects of various fertilization treatments on P changes and sorption isotherms as well as the relationship of soil properties to P sorption and P forms were evaluated in an Ustic Isohumisol, a calcareous soil, on the Loess Plateau, China. Compared to 1984, after 13 years of crop production, total soil P in the no-P treatments （control and N treatment） decreased by 5%-7%, but in the phosphorus fertilizer alone （P）, nitrogen and phosphorus fertilizers in combination （NP）, manure alone （M）, and nitrogen and phosphorus fertilizers and manure in combination （NPM） treatments, it increased by 22%, 19%, 28%, and 58%, respectively. Residual fertilizer P was found mainly in NH4Ac-soluble P （Cas-P）, followed by NaHCO3-soluble P （NaHCO3-P）, and NH4F-soluble P （Al-P）. Phosphorus sorption in the soils with different fertilization practices fit the Langmuir equations. Phosphorus sorption capacity in the no-P treatments increased, whereas it decreased in the P-included treatments （P, NP, and NPM treatments）. Phosphorus sorption maximum （Qm） was significantly and negatively correlated to inorganic P including NaHCO3-P, Cas-P, NaOH-Na2CO3-soluble P （Fe-P）, and Al-P （P ≤ 0.01）. Moreover, long-term fertilization increased soil organic carbon in the NP, M, and NPM treatments and decreased pH in the NP and NPM treatments. Thus, the ability of the soil to release sorbed P to the environment increased under long-term P fertilization.     

可变电荷土壤表面酸碱模型及其计算机模拟

在假定土壤对酸碱的缓冲作用全由表面基团反应所控制的基础上,建立了一个描述可变电荷土壤酸碱滴定曲线的模型,并在计算机上对实验结果进行了模拟。结果表明,本模型可以较好地描述土壤酸碱滴定曲线,提供土壤的酸强度(K_a)和酸容量(S_t),并可进一步提供土壤的酸缓冲容量曲线。本模型对了解和认识土壤酸化和吸附等过程具有一定的意义。