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.     

印度Chattisgarh州两种新开发土和一种淋溶土中磷酸盐吸附-解析特征研究

Two Inceptisols and an Alfisol of the Indravati Catchment area in Chattisgarh, India, comprising several gradients in physical and chemical properties were studied to relate phosphate sorption and desorption to soil properties. From the P isotherm curve, the standard P requirement （SPR） of the soils was determined. Phosphate sorption data were also fitted both to the Langmuir and Freundlich Equations. The mean sorption maximum values for three different soil series were： Bastar 〉 Geedam 〉 Mosodi. The fraction of added phosphate sorbed for the 3 series followed this same trend as did SPR; the phosphate sorption maximum and the maximum phosphate buffering capacity, which were estimated by the Langmuir isotherm; and the Freundlich constant 1/n. However, phosphate desorption, as well as the maximum recovery percent did not follow this order. The phosphate affinity constant （K） was also different following the same progression for the 3 soil series as the Freundlich constant K＇, which measured sorption strength. Meanwhile, an inverse order existed for K and K＇ versus the percent desorbed relative to the sorbed as well as the maximum recovery percent. In addition, significant correlation coefficients among sorption parameters of P and soil factors were found.     

模拟降雨条件下聚丙烯酰胺应用对径流、侵蚀和土壤养分流失的影响

Soil erosion affects soil productivity and environmental quality.A laboratory research experiment under simulated heavy rainfall with tap water was conducted to investigate the effects of anionic polyacrylamide(PAM) application rates(0,0.5,1.0,and 2.0 g m-2) and molecular weights(12 and 18 Mg mol-1) on runoff,soil erosion,and soil nutrient loss at a slope of 5°.The results showed the two lower rates of PAM application decreased runoff while the highest rate increased runoff as compared with the control.Sediment concentration and soil mass loss increased significantly with the increasing PAM application rate.Compared with the control,PAM application decreased K+,NH4+,and NO3-concentrations in sediment and K+ and NH+4 concentrations in runoff,but significantly increased the mass losses of K+,NH4+,and NO-3 over soil surface except for the NH4+ at PAM application rate lower than 1.0 g m-2.PAM application decreased the proportion of K+ loss with runoff to its total mass loss over soil surface from 60.1% to 16.4%.However,it did not affect the NH4+ and NO3-losses with runoff,and more than 86% of them were lost with runoff.A higher PAM molecular weight resulted in less soil erosion and K+ mass loss but had little effect on runoff and NH+4 and NO3-losses.PAM application did not prevent soil erosion and the mass losses of K+ and NO3-under experimental conditions.     

土层性质对铜和铅在土壤中保持和迁移的影响

The mobility and bioavailability of heavy metals in soils is largely governed by sorption and desorption phenomena.Cu2+ and Pb2+ are among the most potentially toxic heavy metals and they are present,often concomitantly,in many polluting spills and in agrochemicals.The objective was to assess and compare the competitive sorption and desorption capacities and sorption hysteresis of Cu2+ and Pb2+,as well as their migration through the profiles of four natural soils:a Humic Umbrisol,an Umbric Cambisol,an Endoleptic Luvisol and a Humic Cambisol.In all horizons Pb2+ was invariably sorbed and retained to a greater extent than Cu2+.The sorption and retention of Cu2+ were most in?uenced by pH,e?ective cation exchange capacity(CECe) and Mn oxide content.On the other hand,the fixation capacity of Pb2+ was most in?uenced by pH,CECe,and Mn oxide and organic matter contents.pH and CECe were the individual soil properties most markedly in?uencing Cu2+ and Pb2+ sorption and retention.In all the horizons Pb2+ exhibited greater hysteresis than Cu2+.In each soil the hysteresis in the A horizon was greater than that in the B horizon,except in the Bt horizon of the Endoleptic Luvisol,due to its high pH and vermiculite content.Based on migration indices,Pb2+ was less mobile than Cu2+ in the studied soils.     

农田土壤中氮同位素分级与硝化能力的关系研究

A laboratory-based aerobic incubation was conducted to investigate nitrogen(N) isotopic fractionation related to nitrification in five agricultural soils after application of ammonium sulfate((NH4)2SO4). The soil samples were collected from a subtropical barren land soil derived from granite(RGB),three subtropical upland soils derived from granite(RQU),Quaternary red earth(RGU),Quaternary Xiashu loess(YQU) and a temperate upland soil generated from alluvial deposit(FAU). The five soils varied in nitrification potential,being in the order of FAU YQU RGU RQU RGB. Significant N isotopic fractionation accompanied nitrification of NH+4. δ15N values of NH+4 increased with enhanced nitrification over time in the four upland soils with NH+4 addition,while those of NO-3 decreased consistently to the minimum and thereafter increased. δ15N values of NH+4 showed a significantly negative linear relationship with NH+4-N concentration,but a positive linear relationship with NO-3-N concentration. The apparent isotopic fractionation factor calculated based on the loss of NH+4 was 1.036 for RQU,1.022 for RGU,1.016 for YQU,and 1.020 for FAU,respectively. Zero- and first-order reaction kinetics seemed to have their limitations in describing the nitrification process affected by NH+4 input in the studied soils. In contrast,N kinetic isotope fractionation was closely related to the nitrifying activity,and might serve as an alternative tool for estimating the nitrification capacity of agricultural soils.     

不同氧化还原条件下土壤性质对非石灰性土壤中锌溶解动力学的影响

Zinc(Zn) deficiency in paddy soils is often a problem for rice production.Flooding can decrease metal availability in some noncalcareous soils through different mechanisms associated with soil redox status.Laboratory experiments were performed in order to better understand the processes that governed the dynamics of Zn in non-calcareous paddy soils at varying redox potentials(Eh).Airdried non-calcareous soil samples collected from four different paddy field sites in the Philippines were submerged and incubated in a reaction cell with continuous stirring and nitrogen purging for 4 weeks,and then purged with compressed air for another week to reoxidize the system.The Eh of the four soils started at 120 to 300 mV,decreased to —220 to —300 mV after 100 to 250 h of reduction,and was maintained at this low plateau for about 2 weeks before increasing again upon reoxidation.Zinc solubility showed contrasting patterns in the four soils,with two of the soils showing a decrease in soluble Zn as the Eh became low,probably due to zinc sulfide(ZnS) precipitation.In contrast,the other two soils showed that Zn solubility was maintained during the reduced phase which could be due to the competition with iron(Fe) for precipitation with sulfide.Differences in the relative amounts of S,Fe,and manganese(Mn) oxides in the four soils apparently influenced the pattern of Zn solubility after flooding.     

Effect of Continuous Vegetable Cultivation on PhosphorusLevels of Fluvo-Aquic Soils

oil P status, inorganic P fractions, and P sorption properties were studied using sandy fluvo-aquic horticultural soils,which are high in organic matter content for vegetable production in comparison with a soil used for grain crop productionin Zhengzhou, Henan Province, China. P fractions, Olsen-P, and OM were determined at different depths in the soilprofile and sorption isotherm experiments were performed. Most P in excess of plant requirements accumulated in thetopsoil and decreased with soil depth. Total P, inorganic P, and OM concentrations increased with continued horticulturaluse.Olsen-P concentrations in the 0-20 cm depth of horticultural soils were 9 to 25 times higher than those of the graincrop soil. A linear transformation of the Langmuir equation showed that the P adsorption maximum (491.3 mg P kg^-1)and the maximum phosphate buffering capacity (162.1 L kg^-1) for 80-100 cm were greater in the grain crop soil than thehorticultural soils. Thus, the most immediate concern with excess P were in areas where heavy P fertilizer was used forvegetable crops and where soil P sorption capacities were low due to sandy soils and high organic matter content.     

Dicyandiamide sorption-desorption behavoir on soils and peat humus

The sorption-desorption behavior of dicyandiamide (DCD) is an important chemical process that affects DCD fate and mobility in soils. Therefore, this study quantified DCD sorption-desorption on a phaeozem (Mollisol), a burozem (Alfisol), a soil with organic matter-removed and peat humus using the batch-equilibration procedure, and identified soil properties that influenced DCD sorption. The sorption on peat humus was higher than that on the phaeozem and the burozem, with much lower sorption observed on the soil with organic matter-removed, indicating that soil organic matter was the main carrier of DCD sorption. Due to its amphipathic property the DCD molecule sorption on the phaeozem and the burozem decreased as pH increased from about 2 to 5, but a further increase in pH led to a rise in DCD sorption.The DCD desorption hysteretic effect for peat humus was greater than that for the phaeozem and the burozem using 0.01 mol L^-1 CaCl2 as the background electrolyte, suggesting that the hydrophobic domains of organic matter may play an important role in DCD sorption.     

Effect of Electrolytes on Surface Charge Characteristics of Red Soils

The zero point of charge (ZPC) and the remaining charge σp at ZPC are two important parameters characterizing surface charge of red soils.Fourteen red soil samples of different soil type and parent material were treated with dithionite-citrate-dicarbonate (DCB) and Na2CO3 respectively.ZPC and σp of the samples in three indifferent electrolytes (NaCl,Na2SO4,and NaH2PO4) were determined.Kaolinite was used as reference.The results showed that ZPC of red soils was affected by the composition of parent materials and clay minerals and in significantly positive correlation with the content of total iron oxide (Fet),free iron oxide (Fed),amorphous iron oxide (Feo),aluminum oxide (Alo) and clay,but it was negatively correlated with the content of total silica (Sit).The σp of red soils was also markedly influenced by mineral components.Organic components were also contributing factor to the value of σp.The surface charges of red soils were evidently affected by the constitution of the electrolytes.Specific adsorption of anions in the electrolytes tended to make the ZPC of red soils shift to a higher pH value and to increase positive surface charges of the soils,thus leading to change of the σp value and decrease of the remaining net negative charges,even to the soils becoming net positive charge carriers.The effect of phosphate anion was greater than that of sulfate ion.     

有机配体、竞争阳离子和pH对土壤中Zn分解的影响

A series of experiments were conducted to examine the interactive effects of an organic ligand, a competing cation, and pH on the dissolution of zinc （Zn） from three California soils, Maymen sandy loam, Merced clay, and Yolo clay loam. The concentrations of soluble Zn of the three soils were low in a background solution of Ca（NO3）2. Citric acid, a common organic ligand found in the rhizosphere, was effective in mobilizing Zn in these soils; its presence enhanced the concentration of Zn in soil solution by citrate forming a complex with Zn. The ability of Zn to form a complex with citric acid in the soil solution was dependent on the concentration of citric acid, pH, and the concentration of the competing cation Ca^2＋. The pH of the soil solution determined the extent of desorption of Zn in solid phase in the presence of citric acid. The amounts of Zn released from the solid phase were proportional to the concentration of citric acid and inversely proportional to the concentration of Ca（NO3）2 background solution, which supplied the competing cation Ca^2＋ for the formation of a complex with citrate. When the soil suspension was spiked with Zn, the adsorption of Zn by the soils was retarded by citric acid via the formation of the soluble Zn-citrate complex. The dissolution of Zn in the presence of citric acid was pH dependent in both adsorption and desorption processes.     

第四纪红色粘土发育的红壤中营养元素的淋失

A red soil derived from Quaternary red clay was employed to study nutrient leaching with soil columns repacked in laboratory. The objective was to identify the effects of fertilization practices on leaching patterns and magnitudes of Ca²⁺, Mg²⁺, K⁺, NH₄⁺, and NO₃^-. The treatments were CK (as a control), CaCO₃, CaSO₄, MgCO₃, Ca(H₂PO₄)₂, urea, KCl, and multiple (a mixture of the above-mentioned fertilizers). The fertilizers were added to the bare surface of the soil columns, and then the columns were leached with 120 mL deionized water daily through peristaltic pumps over a period of 92 days. Leaching processes of NH₄⁺, and NO₃^- were only measured in CK, urea, and multiple treatments which were directly related to N leaching. Results showed that sole application of CaSO₄, and Ca(H₂PO₄)₂ scarcely had any effect on the leaching losses of Ca²⁺, Mg²⁺, and K⁺; the application of MgCO₃ stimulated the leaching of Mg²⁺; the application of CaCO₃ promoted the leaching of Ca²⁺, Mg²⁺ and K⁺; urea treatment also promoted the leaching of K⁺ and NH₄⁺, and NO₃^- leaching mainly occurred at late stage of leaching process in particular; under KCl treatment, leaching of Ca²⁺, Mg²⁺, and K⁺ was promoted to a large extent; under multiple treatment, leaching of Ca²⁺, Mg²⁺, K⁺, NH₄⁺, and NO₃^- was all increased and NO₃^- was mainly leached at the end of leaching process and still had a trend of increase.     

Chemical Composition of Urban Wet Deposition in Amman,Jordan

Precipitation events were collected during the period from October 1996 to April 1997 from two sites in the city of Amman, Jordan. The samples were analyzed for major cations (Na+, K+, Ca2+, Mg2+ and NH4+), major anions (F-, Cl-, NO3- and SO42-), in addition to heavy metals (Cu2+, Cd2+, Zn2+, and Pb2+). High levels of Ca2+ and SO42- were observed. The results were comparable with some regional values and they indicate that about 58% of Na+ and Cl- are of marine origin, while Ca2+, K+ and a large fraction of SO42- are of soil dust origin. Heavy metals were detectable in most of the samples, zinc showed the highest concentrations. Significant correlation was obtained between zinc and lead, which may indicate automobile emission source.     

Effect of ammonium sulfate, ammonium chloride and root-zone acidity on inorganic ion content of tobacco

Tobacco plants (Nicotiana tabacum L. cv NC82) were supplied with (NH4)2SO4 or NH4Cl at root-zone pH of 6.0 and 4.5 in hydroponic culture for 28 days. Dry matter accumulation, total N and C content, and leaf area and number were not affected by the NH4+ source or root-zone pH. Plants supplied with NH4Cl accumulated up to 1.2 mM Cl g DW-1, but accumulated 37% less inorganic H2PO4- and 47% less SO4(2-) than plants supplied with (NH4)2SO4. The large Cl- accumulation resulted in NH4Cl- supplied plants having a 31% higher inorganic anion (NO3-, H2, PO4-, SO4(2-), and Cl-) charge. This higher inorganic anion charge in the NH4Cl-supplied plants was balanced by a similar increase in K+ charge. Plants supplied with NH4Cl accumulated greater concentrations of Cl- in leaves (up to 5.1% of DW) than plants supplied with (NH4)2SO4 (less than -% DW). Despite the high Cl- concentration of leaves in NH4Cl supplied plants, these plants showed no symptoms of Cl- toxicity. This demonstrates that toxicity symptoms are not due solely to an interaction between high Cl- concentration in tissue and NH4+ nutrition. The increase in root-zone acidity to pH 4.5 from 6.0 did not induce toxicity symptoms.     

恒电荷土壤及可变电荷土壤与离子间相互作用的研究 I.共存离子对NO_3~-吸附的影响

研究了我国典型３种可变电荷土壤和４种恒电荷土壤在陪伴阳离子分别为Ｋ十、Ｎａ十、Ｃａ２＋时和１ｍｍｏｌＬ－１ＫＣ１、Ｋ２ＳＯ４支持电解质中ＮＯ３－的吸附。结果表明，ＮＯ３－吸附量随ｐＨ的增加而减小。在添加相同浓度ＮＯ３－时，３种可变电荷土壤对ＮＯ３－的吸附量顺序为Ｃａ（ＮＯ３）２＞ ＫＮＯ３＞ＮａＮＯ３＞ＫＮＯ３十ＫＣＩ＞ＫＮＯ３＋Ｋ２ＳＯ４；在初始ＮＯ３－浓度０．５－５ｍｍｏｌＬ－１的范围内，吸附量随浓度变化的关系符合Ｌａｎｇｍｕｉｒ等温吸附式．由此求出与ＮＯ３－吸附结合能有关的常数（Ｋ）在不同共存离子存在下数值较小且差异不大，因此认为不同陪伴阳离子和不同伴随阴离子对ＮＯ３－吸附的电性机理影响不大，只是改变了土壤表面的正电荷数量从而使吸附量发生变化。４种恒电荷土壤对ＮＯ３－的吸附量通常很小，其中在Ｃａ（ＮＯ３）２介质中较在其他介质中稍大，最大吸附量仅为１．５～ｍｍｏｌ ｋｇ－１左右，约为可变电荷土壤的１／１０，且在浓度较低时常观察到负吸附。     

磷钾肥施用对日光温室土壤溶液离子组成的影响

采用土培模拟试验研究了施用磷、钾肥对大田和温室土壤溶液电导率（EC）、离子含量及其比例的影响。结果表明,温室栽培土壤溶液EC、K+、Na+、Ca2+、Mg2+、NO3-含量以及K+ / Ca2+、K+ / Mg2+摩尔比分别为大田土壤的2.5、95.0、16.6、1.9、3.2、4.0、31.0和39.0倍,说明日光温室土壤离子累积及养分比例失调问题突出。施用磷、钾肥对土壤溶液中不同离子含量的影响不同,增加磷肥施用量,显著降低了大田和温室土壤溶液EC和Ca2+、Mg2+离子含量,而对土壤溶液K+、NO3--N和NH4+-N离子浓度均无显著影响;随施钾量增加,大田及温室土壤溶液EC、K+、Na+、Ca2+、Mg2+和K+/Ca2+、K+/Mg2+摩尔比均呈显著增加趋势。温室栽培实践中因过量施用磷、钾肥而造成的阳离子养分比例失调而带来的营养及生态环境问题值得关注。     

草酸青霉菌HB1溶磷能力及作用机制

一些功能微生物具有溶磷能力且同一菌株对不同难溶性磷酸盐的溶解能力存在差异。该研究以草酸青霉菌HB1为研究对象,通过固体平板培养试验、摇瓶培养试验和土壤培养试验系统研究了不同磷源(磷酸钙、磷矿粉、磷酸铁、磷酸铝)与氮源(铵态氮、硝态氮)供应下HB1溶磷能力及其作用机制,并验证了其在高、低不同磷水平土壤中的溶磷能力。结果表明,接种HB1的不同磷源培养基上均有溶磷圈出现,根据溶磷圈直径/菌落直径初步确定HB1溶解磷酸钙的能力较强;摇瓶培养试验表明供试磷源为磷酸钙、磷酸铁时HB1发酵液中有效磷含量为884、265 mg/L(铵态氮),或945、206 mg/L(硝态氮),其溶磷能力不受氮源形态影响;磷矿粉为磷源时,HB1发酵液中有效磷含量可达199 mg/L(供应铵态氮),为硝态氮供应的7.14倍;而磷酸铝为磷源时,HB1发酵液中有效磷含量为120 mg/L(供应硝态氮),为铵态氮供应的3.29倍;此外,供应铵态氮条件下,HB1对难溶性磷酸盐的溶解能力与介质中pH值呈显著的负相关关系。HB1接种于不同磷水平的土壤中培养21 d,在低磷和高磷土壤中HB1均能有效定殖且增加了土壤有效磷含量,比不接菌对照分别增加45.00%和14.17%。综上,草酸青霉菌HB1对磷酸钙和磷矿粉的溶磷效果较好,并通过分泌氢质子酸解含磷矿物实现溶磷作用,且HB1在低磷土壤中溶磷能力较强。     

菜园土壤锌的吸附——解吸特性研究

本文研究了菜园土壤锌的吸附 -解吸特性。实验结果表明 ,三种菜园土壤吸附Zn2 + 均随平衡液中Zn2 + 浓度的增加而增大 ,且均可用Langmuir方程和Freundlich方程来描述 ,相关系数均大于 0 .9,达极显著水平。由Langmuir方程求得的菜园土壤对Zn2 + 的最大吸附量的大小顺序为 :黄松土 >粉泥土 >江涂砂 ,但对Zn2 + 的吸附作用力强度和最大缓冲容量的顺序则相反 ,以江涂砂 >粉泥土 >黄松土。菜园土壤对Zn2 + 的解吸量随其吸附量的增加而增加 ,两者之间呈显著线性正相关。     

不同施肥对城郊菜地土壤质量、叶菜镉及养分含量的影响

通过田间试验研究不同施肥处理对广州市郊菜地土壤质量、叶菜可食部分Cd含量和养分含量的影响。结果表明:与75kg N/hm2处理相比,150kg N/hm2处理没有显著提高叶菜产量,且后者叶菜地上部分Cd含量较前者有不同程度提高。N用量为75kg/hm2时,硝酸铵+磷酸二氢钙+硫酸钾配施处理的芥菜和小白菜产量较高,矿质养分含量较高,Cd含量较低,且土壤肥力和质量得到维持。因此,在试验条件下,以硝酸铵+磷酸二氢钙+硫酸钾配施处理且N,P2O5,K2O用量分别为75,21.75,67.5kg/hm2时有利于改善叶菜品质和安全;而精制有机肥可能提高土壤和叶菜可食部分Cd含量的风险。     

增铵营养对番茄植株伤流液组分及含量的影响

在总氮(N)浓度相等的条件下,研究全硝营养(100% NO3-)和25% 增铵营养(NH4+∶NO3- = 25%∶75%)对开花期和幼果期番茄植株伤流液各组分含量的影响.结果表明,增铵营养显著增加幼果期伤流液中 K的含量,对Ca、Mg、P元素含量没有显著影响;增铵营养下伤流液中 NO3- 的含量下降、NH4+ 含量增加,氨基酸、苹果酸等的含量均显著增加,氨基酸/硝态氮含量之比显著提高,表明喜硝作物适当增铵不仅能够提高根系活力,显著促进K的吸收以供果实发育之需,而且提高了植株整体同化N素的能力.     

Effect of pH on Zinc Sorption–Desorption by Soils

The objective of this study was to examine the effect of soil pH on zinc (Zn) sorption and desorption for four surface soils from the Canterbury Plains region of New Zealand. Zinc sorption by the soils, adjusted to different pH values, was measured from various initial solution Zn concentrations in the presence of 0.01 M calcium nitrate [Ca(NO₃)₂]. Zinc desorption isotherms were derived from the cumulative Zn desorbed (µg g^?1 soil) after each of 10 desorption periods by sequentially suspending the same soil samples in fresh Zn‐free 0.01 M Ca(NO₃)₂. Zinc sorption and desorption varied widely with soil pH. Desorption of both native and added Zn decreased continuously with rising pH and became very low at pH values greater than 6.5. The proportion of sorbed Zn that could be desorbed back into solution decreased substantially as pH increased to more than 5.5. However, there were differences between soils regarding the extent of the hysteresis effect.