有机质和陪伴阴离子对土壤吸附Zn的影响

本文研究了土壤有机质和陪伴阴离子对黄棕壤、红壤和砖红壤吸附Zn²⁺的影响。结果表明:土壤有机质含量与吸附Zn²⁺的数量呈正相关;陪伴阴离子对土壤吸Zn²⁺量有显著的制约作用,土壤从ZnCl₂溶液中吸附的Zn²⁺数量高于Zn(NO₃)₂的0.77-1.16倍;△pH值与吸Zn²⁺量呈直线关系。由解吸情况可以判明红壤胶体表面的高能吸附位占的比例明显大于黄棕壤或砖红壤。     

有机阴离子对磷酸根吸附的影响

在中性条件下,低浓度的柠檬酸、草酸、酒石酸和胡敏酸阴离子都能显著降低针铁矿、非晶氧化铝、高岭石和红壤对磷酸根的吸附,尤其在低磷吸附饱和度下效果更好。有机阴离子抑制磷酸根吸附的能力因有机酸的种类和性质、以及固相的表面特性而异。有机阴离子存在下吸附的磷酸根具有较高的同位素³²P交换活性和解吸率。测定了吸附平衡溶液中铁和铝的浓度。结果表明,在实验条件下(pH 7.0),即使较高浓度的有机酸根(10^-2mol)也只能溶解极少量的铁和铝。有机阴离子络溶作用不足以说明固相吸附磷能力的显著下降。可见,有机阴离子降低磷酸根吸附的机制主要是竞争专性吸附。有机阴离子占据了一部分高亲和力的吸附位,从而降低了土壤固相吸附磷的量,增加了吸附态磷的活性。     

90℃下老化时结晶磷铁矿的生成条件

溶液中Fe与P反应并不直接生成结晶磷铁矿,中间经过无定形阶段。溶液的pH对Fe-P无定形物质的组成及由无定形Fe-P向结晶磷铁矿转化都有很重要的作用。在90°下老化80天,用加入的Fe(NO₃)₃和NaH₂PO₄浓度及混合后的溶液pH计算得到的﹝Fe³⁺﹞﹝H²PO₄^-﹞值可以较好地判断溶液中是否会有结晶磷铁矿生成。本文的实验条件下,结晶磷铁矿生成的条件是-log{﹝Fe³⁺﹞﹝H₂PO₄^-﹞} ≤ 6.09(加入的P/Fe比 ≥ 1)。     

淹水条件下施加石灰和有机质对酸性土壤性质和磷吸附的影响

每公斤土加入2克碳酸钙和(或)三叶草的5个老成土和1个氧化土,在淹水培育45天后风干,结果发现:(1)淹水土壤风干,其pH比淹水时低,但仍比未淹水的高;(2)淹水降低了土壤中0.5MCuCl₂提取的铝量,石灰和三叶草处理使3个轻质土中的铝量进一步降低,但3个粘质土则呈现相反的趋势;(3)改良剂使3个轻质土吸附的磷减少,而使3个粘质土吸附的磷增加。前者增加的原因是因为通过还原作用和氧化作用形成了较多的活性表面,而后者的减少则可能是粘粒表面所形成的水化氧化物胶膜堵塞了原有的吸附位,从而使吸附位减少(4)改良剂对磷解吸的影响,是降低了3个轻质土的磷解吸,而增加了3个粘质土的磷解吸;(5)经淹水风干处理土壤的磷吸附量与草酸盐提取的铁、铝、锰及CuCl₂溶液提取的铝有很高的相关性,表明控制淹水土壤磷吸持的土壤组分,不仅包括无定形铁,而且也包括羟基铝聚合物。     

施磷对玉米吸磷量、产量和土壤磷含量的影响及其相关性

为了给玉米磷高效利用提供理论依据, 在低磷土壤(Olsen-P 4.9 mg·kg^-1)上, 通过田间试验, 研究了施磷0(T₀)、50 kg(P₂O₅)·hm^-2(T₁)、100 kg(P₂O₅)·hm^-2(T₂)、200 kg(P₂O₅)·hm^-2(T₃)、1 000 kg(P₂O₅)·hm^-2(T₄)对两个玉米品种"鲁单9002" (LD9002)、"先玉335"(XY335)的产量、磷素吸收利用及根际磷动态变化的影响。结果表明: 两玉米品种根际土、非根际土速效磷含量在不同生育时期都表现为T12O₅)·hm^-2的T₃处理非根际土转化为根际土土壤磷的量最大, 同时玉米生物量、产量、磷转移量也达到最高, 而施磷1 000 kg(P₂O₅)·hm^-2处理玉米生物量、产量与中磷水平相比没有显著增加, 但植株吸磷量较高。XY335的花后磷转移量小于LD9002。相关分析表明, LD9002根际土、非根际土速效磷含量与茎、叶吸磷量之间显著相关, 以播种后79 d与茎、叶磷浓度、吸磷量、生物量、产量之间的相关系数最高; 而XY335根际土、非根际土速效磷含量与茎、叶磷浓度之间显著相关, 在播种后47 d期间与茎、叶磷浓度、吸磷量、生物量、产量之间的相关性最好。因此, 在低磷土壤上, LD9002和XY335分别在播种后79 d和47 d时是植株对磷的敏感期, 可以通过测试根际土、非根际土速效磷含量来反映土壤的供磷状况; LD9002在79 d时最大吸磷量需要的根际土、非根际土速效磷含量分别为54.95 mg·kg^-1、32.99 mg·kg^-1, XY335品种在47 d时最大吸磷量需要的根际土、非根际土速效磷含量分别为51.24 mg·kg^-1、35.35 mg·kg^-1; 施磷量1 000 kg(P₂O₅)·hm^-2处理两品种玉米产量、生物量、磷积累量与施磷量100~200 kg(P₂O₅)·hm^-2处理没有显著差异。     

用铜电极电位滴定法测定土壤交换性铝

以Cu²⁺电极为指示电极,用间接电位滴定法测定溶液中的铝,其相对误差小于2.0%。为加速反应,并使络合反应进行完全,应加入过量EDTA,并将溶液加热至沸。实验结果还表明,土壤中Ca²⁺,Mg²⁺,Mn²⁺,Fe³⁺对测定不发生干扰。当土壤中交换性铝的含量为0.03-8mc/100g时,本法测定的相对误差低于5.0%,与经典的中和法相比,本法操作简便,终点易于判断,精密度更高。     

影响土壤镉吸持和解吸的因子

研究了土壤的pH、离子浓度(0.01mol/L、0.05mol/L、0.1mol/L)、阴(阳)离子种类(NO₃^-、Cl^-、OAc^-、SO₄^2-、HPO₄^-及Zn和Pb)及石灰和葡萄糖对土壤镉吸持及其解吸的影响。     

镁对土壤某些理化性质的影响

本文研究了镁离子在土壤中的吸附特性和交换性镁对土壤某些物理性质的影响。试验结果表明:镁盐阴离子对镁离子侵入土壤吸收复合体能力的影响为:CO₃^2->SO₄^2->Cl^-。在低浓度下,Mg²+在Na⁺陪伴下较其单独存在时更易被含MgCO₃的石灰性土壤吸附。在混合盐溶液中,当盐渍度和SAR一定时,Na⁺在Na⁺-Mg²⁺体系中比在Na⁺-Ca²⁺体系中更易被土壤吸附。当ESP一定时,随着土壤吸收复合体中交换性镁百分率(EMP)的增加,分散系数逐渐增加,饱和导水率和毛管水上升高度逐渐降低,当EMP>60%时,不再发生变化。随着ESP的增加,交换性镁的不良影响逐渐变小。     

在DAP-CaCO3体系与DAP-石灰性土壤体系中NH3的挥发与磷的吸附之间的关系

本工作是研究在CaCO₃体系和石灰性土壤体系中NH₃的挥发与磷的吸附之间相互作用的化学变化,结果表明:在NH₄Cl—CaCO₃体系中,通气的pH值比不通气的低,但溶液中Ca²⁺浓度正好相反。在K₂HPO₄-CaCO₃体系中,在24小时内,通气与不通气的,CaCO₃吸附磷没有差异。在24小时反应期间,在DAP-CaCO₃体系中,因溶液pH值不断增高,NH₃的挥发对CaCO₃吸附磷的影响也就逐渐降低。在石灰性土壤体系中,施用尿素加过磷酸钙或单施尿素时,几乎没有发现NH₃的挥发,而施DAP时,在6天后,NH₃的挥发损失占加入的56%,且DAP处理的土壤,其水溶性磷未通气比通气的高。尿素加过磷酸钙处理的,其水溶性磷通气与未通气的没有差异。另外,尿素加过磷酸钙或过磷酸钙单独处理的土壤,水溶性磷含量均相同。所有这些均表明,在石灰质体系中,NH₃的挥发(如果发生的话)能够加强CaCO₃对磷的吸附,而磷的吸附又能加强NH₃的挥发,两者是相互影响和相互促进的过程。     

咸水结冰灌溉结合改良剂对滨海盐土的改良作用

冬季咸水结冰灌溉是将冬季自然冷资源与滨海盐碱地区丰富的咸水资源相结合, 通过自然结冰使咸淡分离, 再利用结冰融化时咸水先流出淡水后流出会对土壤起到一定的洗盐作用的原理, 对盐碱地进行改良。本文通过大田试验, 研究了冬季咸水结冰灌溉及改良剂对天津滨海盐碱地水盐运移的影响。结果表明, 通过咸水结冰灌溉能降低根层土壤含盐量, 且灌溉水量与土壤含水量呈正相关。冬季咸水结冰灌溉初期可能会引起土壤碱化, 但随着冰层融化及时间的推移, 各处理的碱化趋势会逐渐消弱。在滨海盐土施用磷石膏能够降低HCO₃^-含量, 增加SO₄^2-、Ca²⁺含量, 有效降低Cl^-、Na⁺在总盐分中的比例, 且磷石膏施用量越大, 根层土壤的pH 越低、保水能力越强(7 500 kg·hm^-2 磷石膏>4 500 kg·hm^-2 磷石膏); 施用磷石膏和大水量的咸水结冰灌溉都能很好地促进柽柳生长,且咸水冬季结冰灌溉和施用磷石膏配合(1 350 m³·hm^-2 结冰灌溉+7 500 kg·hm^-2 磷石膏)效果最好。因此, 咸水结冰灌溉配合改良剂应用可有效改良滨海盐土, 改善因咸水结冰灌溉而带来的土壤碱化问题, 为早期植物萌发生长提供有利条件。     

土壤组分对广东省酸性水稻土磷吸附参数的影响

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.     

Solubility of soil phosphorus as influenced by urea

The objective of this study was to investigate possible ways of mobilizing residual fertilizer P as a result of local pH elevation caused by urea hydrolysis. The response of water-soluble P (P_w) and dissolved organic C (DOC) to urea hydrolysis was monitored in three cultivated soils and at two P levels for up to 127–135 d and compared with corresponding changes in soils limed with Ca(OH)₂. Hydrolysis of urea was complete in 8–15d during which soil pH increased by 1–1.5 units at the maximum. Subsequently, the pH decreased to or below the original level owing to nitrification. Mobilization of soil P was enhanced substantially in parallel with the increase in pH, the peak P_w occurring simultaneously with the highest pH value. In all urea-treated soils, P_w remained at an elevated level for at least 60d. As compared to urea, elevation of soil pH with Ca(OH)₂ had only a minor and inconsistent influence on P_w. In mobilization of soil P, the urea-induced increase in pH and a simultaneous production of NH₄⁺ ions proved to be superior to liming with Ca(OH)₂. It was hypothesized that when an acid soil is amended with urea, phosphate is first displaced by OH^? ions, resulting in elevated solution P concentrations. A simultaneous dissolution of organic matter contributes to the persistence of high P concentration by competition for sorption sites on Fe and Al oxides, and thus retards the resorption of P.     

THE COVARIANCE OF PHOSPHATE SORPTION WITH OTHER SOIL PROPERTIES IN SOME BRITISH AND TROPICAL SOILS

Phosphate sorption capacity estimated by Piper's (1942) ‘anion exchange capacity’ and Bache and Williams's (1971) phosphate sorption index were correlated with soil pH, clay, organic matter, ‘free iron oxides’ and ‘extractable aluminium’ (McLean et al., 1958) for topsoil and subsoil samples from twenty tropical and twenty British acidic soil profiles. These two groups of soils did not differ significantly in phosphate sorption. Extractable aluminium and free iron oxide were well correlated with phosphate sorption, free iron oxide being superior to aluminium in freely drained British soils but not in poorly drained ones. Organic matter content correlated well with phosphate sorption for the poorly drained British soils, and for the tropical soils when sorption capacitywas measured using a high phosphate concentration.     

Effect of liming on phosphate sorption by acid soils

The sorption of phosphate (P) by four strongly acid Fijian soils from 0.01 M CaCl₂ decreased with increasing pH up to pH 5.5–6.0 and then increased again. The initial decrease in P sorption with increasing pH appears to result from an interaction between added P, negative charge, and the electrostatic potential in the plane of sorption. The results of a sorption study, involving KCl or CaCl₂ of varying concentrations as the background electrolyte and using Nadroloulou soil incubated with KOH or Ca(OH)₂, suggested that the increase in P sorption at pH values > 6.0 was caused by the formation of insoluble Ca-P compounds. For some soils this is consistent with the results of an isotopic-exchange study in which incubation with lime caused marked reductions in the amounts of exchangeable P at high pH.     

Cadmium sorption by two acid soils as affected by clearing and cultivation

Abstract

The objective of this study was to determine the effect of clearing and cultivation on the sorption of cadmium (Cd) by two acid soils from Zimbabwe with differing cultivation stories. In their original state, not cleared‐not cultivated (virgin soils), the two soils exhibited noticeable and similar capacities to sorb Cd. The Mazowe soil contains the highest level of organic matter (40 g kg^‐1) and a effective cation exchange capacity (ECEC) of 144 mmol_c kg^‐1. Yet, Bulawayo soil (23.5 g kg^‐1 organic matter and ECEC of 146 mmol_c kg^‐1) has higher pH and Mn and Fe oxide content and these characteristics seemed to counteract the effect of lower organic matter. After 50 years of cultivation, The Mazowe soil has lost 60% of its organic matter and ECEC, and consequently the ability of its soil matrix to bind Cd has proportionally decreased. In Bulawayo (cleared in 1983 and first ploughed in 1984), on the contrary, the organic matter and ECEC of the cultivated soil remains over 95% of the values on its virgin counterpart. In this soil, the retaining ability for Cd has not still been affected. In the two soils Cd sorption was highly pH‐dependent. The extent of sorption was minimal under acidic conditions and increased sharply as the pH was raised. The immediate reversibility of the sorption process proved to be very low. When sorption and desorption data were compared it was clear that soil characteristics like high organic matter and oxide content which showed to enhanced Cd sorption, contributed at the same time to slow down the backward reaction.     

Sorption of phosphorus by some surface soils from Quebec in relation to their properties

Abstract

Surface horizons from Podzolic and Gleysolic soils were collected in various parts of the province of Quebec, Canada, and equilibrated with various amounts of KH₂PO₄ in 0.01 M CaCl₂ for 48 hours. P sorption data conformed to the linear form of the Langmuir and Freundlich equations. P solubility isotherms showed evidence of hydroxyapatite formation in most samples studied, whereas equilibration solutions of only few samples were saturated with respect to either dicalcium phoshate dihydrate or octocalcium phosphate. These reaction products were associated to soil pH and levels of added phosphate. The average values of the Langmuir sorption maximum for these studied Gleysolic and Podzolic samples were 763 and 1096 μg/g respectively. These values were higher than those obtained by the segmented and modified Freundlich models.

Relationships between the soil characteristics and P sorption parameters were evaluated by regression analysis. Among all variables, oxalate‐extractable Fe plus Al content of the Podzolic samples and the ratio of oxalate—extractable Al to clay of the Gleysolic samples gave the best significant correlation coefficients. Furthermore, soil pH and various ratios such as pyrophosphate‐extractable Fe and Al, oxalate‐extractable Fe and organic matter to clay were found to be significantly correlated only with the P sorption parameters of the Gleysolic samples.     

Effect of two moisture regimes on P-release from P treated soils

Understanding phosphorus (P) release under different climatic or moisture regimes will facilitate effective management of plant nutrition. The objective of this study is to evaluate the effect of two soil moisture regimes on P release from Ogun rock phosphate (ORP) and Sokoto rock phosphate (SRP) in two soil types. Soil was poured into soil columns to form lower and top layers. Top layer was mixed with 400 kg ha^?1 P from ORP, SRP, single super phosphate (SSP) and leached with 35.4 cm³ water representing low moisture regime (LMR; 400 mm rainfall) and 106.1 cm³ water for high moisture regime (HMR; 1200 mm rainfall). P concentrations of leachates, available P in soil and soil pH were determined. Cumulative P leached was higher under HMR than LMR in both soils. There was more leaching with SSP (0.41–0.97 mg P) than both phosphate rocks (0.008–0.19 mg P) indicating leaching potential of SSP. Cumulative P leached from SSP treated Olokemeji soils was twice that of acidic Sapoba under LMR while they were similar (Olokemeji, 0.97 mg P; Sapoba, 0.94 mg P) under HMR suggesting that LMR enhances fixation of P in acidic soils. Irrigation of P fertilized soils may reduce P sorption in acidic soils.     

The effects of pH and drying on adsorption of phosphate by aluminium-organic matter associations

The effects of pH value and of drying on phosphate adsorption by Al-peat and Al-humate associations were investigated. Raising the pH of the Al-organic matter associations from 3 to 7, by addition of Ca(OH)₂, greatly increased their phosphate adsorption capacity. There was a pronounced increase in phosphate adsorption as a result of drying the limed, Al-organic matter associations, but when equilibration time was increased phosphate adsorption by moist Al-peat samples approached that of the dried samples, indicating that the drying effect was at least partially caused by incomplete equilibration of P in the moist samples. In contrast, increasing the equilibration time did not alter the magnitude of the pH effect.
A detailed study was made of the adsorption of phosphate both by Al-peat limed to pH 7.0, and by its constituent components Ca-peat (pH 7.0) and hydroxy-Al (pH 7.0), synthesized separately then mixed together. For limed Al-peat, drying increased phosphate adsorption, whereas for the individually synthesized components in combination the reverse was true. Thus, the limed Al-peat behaved differently to its components.
The increasing adsorption of phosphate by Al-organic matter complexes with rising pH was attributed to increasing hydrolysis and polymerization of hydroxy-Al associated with the organic matter. However, the interaction of organic matter with hydroxy-Al would block many phosphate adsorption sites on the hydroxy-Al. Upon drying, it is suggested that the organic matter condenses and the accessibility of phosphate to adsorption sites on the hydroxy-Al is increased. Thus, drying resulted in increased phosphate adsorption.     

Influence of Increasing Soil Copper Concentration on the Susceptibility of Phosphomonoesterase and Urease to Heat Disturbance

The sorption of chromium (Cr) species to soil has become the focus of research as it dictates the bioavailability and also the magnitude of toxicity of Cr. The sorption of two environmentally important Cr species [Cr(III) and Cr(VI)] was examined using batch sorption, and the data were fitted to Langmuir and Freundlich adsorption isotherms. The effects of soil properties such as pH, CEC, organic matter (OM), clay, water-extractable SO₄ ^2– and PO₄ ^3–, surface charge, and different iron (Fe) fractions of 12 different Australian representative soils on the sorption, and mobility of Cr(III) and Cr(VI) were examined. The amount of sorption as shown by K _f was higher for Cr(III) than Cr(VI) in all tested soils. Further, the amount of Cr(III) sorbed increased with an increase in pH, CEC, clay, and OM of soils. Conversely, the chemical properties of soil such as positive charge and Fe (crystalline) had a noticeable influence on the sorption of Cr(VI). Desorption of Cr(VI) occurred rapidly and was greater than desorption of Cr(III) in soils. The mobility of Cr species as estimated by the retardation factor was higher for Cr(VI) than for Cr(III) in all tested soils. These results concurred with the results from leaching experiments which showed higher leaching of Cr(VI) than Cr(III) in both acidic and alkaline soils indicating the higher mobility of Cr(VI) in a wide range of soils. This study demonstrated that Cr(VI) is more mobile and will be bioavailable in soils regardless of soil properties and if not remediated may eventually pose a severe threat to biota.     

Effect of Lime and Flooding on Phosphorus Availability and Rice Growth on Two Acidic Lowland Soils

Abstract

Loss of soil‐water saturation may impair growth of rainfed lowland rice by restricting nutrient uptake, including the uptake of added phosphorus (P). For acidic soils, reappearance of soluble aluminum (Al) following loss of soil‐water saturation may also restrict P uptake. The aim of this study was to determine whether liming, flooding, and P additions could ameliorate the effects of loss of soil‐water saturation on P uptake and growth of rice. In the first pot experiment, two acid lowland soils from Cambodia [Kandic Plinthaqult (black clay soil) and Plinthustalf (sandy soil)] were treated with P (45 mg P kg^?1 soil) either before or after flooding for 4 weeks to investigate the effect of flooding on effectiveness of P fertilizer for rice growth. After 4 weeks, soils were air dried and crushed and then wet to field capacity and upland rice was grown in them for an additional 6 weeks. Addition of P fertilizer before rather than after flooding depressed the growth of the subsequently planted upland rice. During flooding, there was an increase in both acetate‐extractable Fe and the phosphate sorption capacity of soils, and a close relationship between them (r²=0.96–0.98). When P was added before flooding, Olsen and Bray 1‐extractable P, shoot dry matter, and shoot P concentrations were depressed, indicating that flooding decreased availability of fertilizer P. A second pot experiment was conducted with three levels of lime as CaCO₃ [to establish pH (CaCl₂) in the oxidized soils at 4, 5, and 6] and four levels of P (0, 13, 26, and 52 mg P kg^?1 soil) added to the same two acid lowland rice soils under flooded and nonflooded conditions. Under continuously flooded conditions, pH increased to over 5.6 regardless of lime treatment, and there was no response of rice dry matter to liming after 6 weeks' growth, but the addition of P increased rice dry matter substantially in both soils. In nonflooded soils, when P was not applied, shoot dry matter was depressed by up to one‐half of that in plants grown under continuously flooded conditions. Under the nonflooded conditions, rice dry matter and leaf P increased with the addition of P, but less so than in flooded soils. Leaf P concentrations and shoot dry matter responded strongly to the addition of lime. The increase in shoot dry matter of rice with lime and P application in nonflooded soil was associated with a significant decline in soluble Al in the soil and an increase in plant P uptake. The current experiments show that the loss of soil‐water saturation may be associated with the inhibition of P absorption by excess soluble Al. By contrast, flooding decreased exchangeable Al to levels below the threshold for toxicity in rice. In addition, the decreased P availability with loss of soil‐water saturation may have been associated with a greater phosphate sorption capacity of the soils during flooding and after reoxidation due to occlusion of P within ferric oxyhydroxides formed.