3 种挺水植物吸收水体NH4+、NO3-、H2PO4- 的动力学特征比较

本文用动力学试验研究了具有景观价值的3 种挺水植物—— 水生美人蕉(Canna generalis)、细叶莎草(Cyperus papyrus)、紫芋(Colocasia tonoimo)对H₂PO₄^-、NH₄⁺、NO₃^- 的吸收特征及差异。试验结果表明: 3 种挺水植物吸收H₂PO₄^- 时, 美人蕉的吸收速率最快, 且在较低离子浓度条件下也可以吸收该离子, 说明其具有嗜磷特性, 能够适应广范围浓度H₂PO₄^- 环境; 吸收NO₃^- 时, 细叶莎草的速率最快, 但对低浓度NO₃^- 环境的适应能力较差, 美人蕉吸收NO₃^- 的特性与细叶莎草刚好相反; 吸收NH₄⁺ 时, 细叶莎草的吸收速率最快, 且在低浓度NH₄⁺ 环境下仍能吸收该离子, 而美人蕉的吸收速率最慢, 但能在低浓度NH₄⁺ 环境下吸收该离子。说明不同植物对养分的吸收特性存在较大差异, 各自的污染水体修复适用范围也不同。美人蕉可用于各种浓度H₂PO₄^- 污染的水体修复; 而NO₃^- 污染严重的水体最适宜用细叶莎草作先锋植物, 修复到一定程度后再种植美人蕉来维持水质; 细叶莎草在各种浓度NH₄⁺ 污染的水体中均适用, NH₄⁺ 污染较轻的水体也可用美人蕉修复。     

水培条件下CO2与NH+4/NO-3配比对番茄幼苗生育的影响

升高CO₂浓度能够促进作物的光合作用，提高作物的生物量和产量，但关于CO₂与NH⁺₄/NO^-₃比及其交互作用对作物影响的研究较少，为探索番茄幼苗生长发育对CO₂浓度升高的响应是否对NH⁺₄/NO^-₃配比有较强的依赖关系，本试验在营养液栽培条件下，以番茄(Lycopersicun esculentum Mill)为试材，研究正常大气CO₂浓度(360 μL/L)和倍增CO₂浓度(720 μL/L)与不同NH⁺₄/NO^-₃配比的交互作用对番茄幼苗生长的影响。结果表明：CO₂浓度升高提高了低NH⁺₄/NO^-₃比例处理中番茄叶片的光合速率和水分利用率，提高幅度随NH⁺₄/NO^-₃比例的降低而增强，光合速率增强最大达55%。在同一CO₂浓度处理下净光合速率与水分利用率均随NH⁺₄/NO^-₃比例的增加而显著降低。这说明CO₂浓度升高对番茄幼苗生长发育的促进作用随NH⁺₄/NO^-₃比例的降低而提高，但并没有减弱全NH⁺₄-N处理中番茄幼苗的受毒害作用。综上所述，CO₂浓度升高能提高植物生产的节水能力和水分生产力；水培条件下，NO^-₃-N是最适合番茄幼苗生长发育的氮源，其它NH⁺₄/NO^-₃比例对番茄幼苗的生长发育有一定的抑制作用，仅以NH⁺₄-N作氮源则番茄幼苗很难生长。     

Fe2（SO4）3/γ-Al2O3催化剂微波法玉米皮中提肌醇工艺研究

以玉米皮为原料制取菲丁,采用Fe2(SO4)3/γ-Al2O3固体酸催化剂,甘油做为水解促进剂,在常压微波辅助下催化水解菲丁制取肌醇,通过单因素及正交试验确定了最优工艺条件:辐射功率600w、水解时间70min、甘油配比为5、催化剂用量10g,在此条件下肌醇收率为72.69%。     

添加H2O2改性和HNO3/H2SO4改性生物质炭对一种酸性水稻土吸附Cd (Ⅱ)的影响

选择稻草、玉米秸秆和油菜秸秆作为制备生物质炭的原料，分别用H2O2和HNO3/H2SO4对生物质炭进行改性处理，以未改性的生物质炭和HCl处理的生物质炭作为对照。按土重3%的比例向采自安徽郎溪的酸性水稻土中添加上述生物质炭，在经历一个干湿交替周期后，进行Cd(Ⅱ)吸附/解吸实验，研究添加生物质炭对水稻土吸附Cd(Ⅱ)的影响及其机制。结果表明，两种改性方法均有效增加了生物质炭表面的质子结合位点数，且HNO3/H2SO4改性对生物质炭表面羧基官能团的扩增效果更显著。官能团的增加使得添加了HNO3/H2SO4改性生物质炭的水稻土对Cd(Ⅱ)的专性吸附能力显著增强。因此，添加HNO3/H2SO4改性生物质炭可以作为酸性水稻土吸附固定重金属Cd的一种新型方法。     

三种农药对Cu2+在蒙脱石和δ-Al2O3上吸附的影响

本文比较研究了Ｃｕ＾２＋在草甘磷、毒莠定和杀虫脒等三种农药条件下在Ｃａ－蒙脱石和δ－Ａｌ２Ｏ３上的吸附。草甘磷降低了Ｃｕ＾２＋在Ｃａ－蒙脱石上的吸附。当草甘磷／Ｃｕ＾２＋摩尔比越高时，Ｃｕ＾２＋吸附的降低量则越大。草甘磷是通过络合机制而降低Ｃｕ＾２＋在Ｃａ－蒙脱石上的吸附，同时增加了Ｃｕ＾２＋在δ－Ａｌ２Ｏ３上的吸附。当草甘磷／Ｃｕ＾２＋摩尔比越高时，Ｃｕ＾２＋吸附的增加量也就越大。草甘磷作为桥而     

陕西省几种代表性土壤NH4+吸附、解吸动力学特征研究

采用连续液流法测定了五种土壤吸附、解吸ＮＨ＾＋４的动力学性质。研究表明：（１）ＮＨ＾＋４吸附、解吸平衡时间及反应速率，平衡时的吸附、解吸量及吸附平衡常数均随土壤粘粒和ＣＥＣ不同而变化；（２）不同动力学模型及同一模型对不同土壤的拟合性不同。     

Fixed ammonium and potassium release from two soils

Abstract

Release of native and added K⁺ and NH⁺ ₄ from two soils was monitored during a 166 day incubation/leaching experiment. One soil (Brookston) represented a major soil series In Ontario whereas the other (Harriston) was suspected having a relatively large fixation capacity. Treatments were imposed involving addition of 50 μM g^‐1 soil of K⁺(KCl) or NH⁺ ₄ (NH₄Cl) only or one added after the other on successive days. The addition of either K⁺ or NH⁺ ₄ on day 2 tended to inhibit the release of the other added on day I. Also the addition of either K⁺ or NH⁺ ₄ on day 1 tended to inhibit the sorption or fixation of the other on day 2. The release rate of K⁺ during the 10 to 166 day period was almost constant and not affected by the addition of NH⁺ ₄. Alternatively, the addition of K⁺ on day 2 slowed the release rate of NH⁺ ₄ measured by NO^? ₃ appearance from day 10 to 40 but had no effect thereafter. At the end of the experiment considerably more K⁺ than NH⁺ ₄ was retained suggesting that K⁺ was more firmly fixed. However, the continuing nitrification of NH⁺ ₄ must be contrasted with periodic removal of K⁺ by leaching with 0.01 M CaCl₂ solution since the equilibrium between exchangeable and fixed ions was affected. There were no notable differences between the two soils inspite of a considerable difference in clay content.     

Effect of residence time on the kinetics of nonexchangeable ammonium release from illite and vermiculite

The fraction of nonexchangeable ammonium (NH₄⁺) can play an important role in N cycling of soils as a sink (fixation) or a source (release) of NH₄⁺. Recently fixed nonexchangeable NH₄⁺ especially seems to be a significant source for N release. The aim of our study was to determine the effect of residence time on the kinetics of nonexchangeable NH₄⁺ release from illite and vermiculite. Calcium-saturated illite and vermiculite, containing NH₄⁺ that was “fixed” for one and 60 d, were extracted with a H-resin for 0.25 to 384 h. Both clay minerals “fixed” significantly more NH₄⁺ in 60 d than in 1 d, but vermiculite “fixed” more NH₄⁺ than illite. The kinetics of nonexchangeable NH₄⁺ release from illite and vermiculite were well described by the Elovich equation and by a heterogeneous diffusion model. In vermiculite the percentage of nonexchangeable NH₄⁺ release decreased from 84% to 78% when the time of fixation increased from 1 to 60 d. In illite time of residence has not influenced the complete release of newly fixed NH₄⁺.     

Variation in the relationship between nitrification and acidification of subtropical soils as affected by the addition of urea or ammonium sulfate

The effects on nitrification and acidification in three subtropical soils to which (NH₄)₂SO₄ or urea had been added at rate of 250 mg N kg⁻¹ was studied using laboratory-based incubations. The results indicated that NH₄⁺ input did not stimulate nitrification in a red forest soil, nor was there any soil acidification. Unlike red forest soil, (NH₄)₂SO₄ enhanced nitrification of an upland soil, whilst urea was more effective in stimulating nitrification, and here the soil was slightly acidified. For another upland soil, NH₄⁺ input greatly enhanced nitrification and as a result, this soil was significantly acidified. We conclude that the effects of NH₄⁺ addition on nitrification and acidification in cultivated soils would be quite different from in forest soils. During the incubation, N isotope fractionation was closely related to the nitrifying capacity of the 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.     

Correction of iron chlorosis in peanut (arachis hypogea shulamit) by ammonium sulfate and nitrification inhibitor

Peanut (Arachis hypogea cv. Shulamit) grown on very high calcium carbonate (CaCO₃) content soils is showing iron (Fe) chlorosis symptoms. Supplying the plant with ammonium sulphate ((NH₄)₂SO₄) in the presence of nitrapyrin (N‐Serv) for preventing nitrification reduced Fe chlorosis. Nitrate (NO^‐ ₃) developed in the soil with time, even with nitrapyrin present. When ammonium (NH⁺ ₄) was even less than 20% of the total mineral N in the soil, no Fe‐stress could be observed, suggesting that the NH⁺ ₄ uptake by the plant and the consequence of hydrogen (H⁺) efflux occurs from the root to the rhizosphere, resulting in a decrease of redox potential near the root, and solubilizing enough Fe near the root to overcome the chlorosis.     

不同铵钾比对高铵下拟南芥地上部和根系生长的影响

钾在缓解植物铵毒害的过程中起着重要的作用。本文研究了高铵(30 mmol/L)条件下,不同铵钾比(7.5︰1和150︰1)对拟南芥(Col-0)主根、侧根以及地上部生长的影响。结果表明:30 mmol/L NH4+条件下,高铵钾比(150)处理显著加重了拟南芥铵毒害现象,地上部和根系生长所受的抑制作用更为明显并导致更严重的氧化胁迫。相比低铵钾比水平,在高铵处理下,高铵钾比使得拟南芥主根伸长量降低57.4%,侧根数量减少33.3%,而地上部鲜重减轻69.9%。DAB(3,3￠-二氨基联苯胺,3,3￠-diaminobenzidine)叶片染色结果表明,不加铵处理下,外源不同钾水平(0.2和4.0 mmol/L)对拟南芥叶片的氧化胁迫作用没有显著差异;而高铵处理下,相比低铵钾比处理,高铵钾比显著增加了叶片中过氧化氢的含量,加重了其氧化胁迫。伊文思蓝(Evans blue,EB)染色结果表明,不加铵处理下,外源不同钾水平对拟南芥地上部和根部的膜透性没有显著差异,而高铵处理下,高铵钾比显著增强了拟南芥地上部和根部的膜透性,表明其对细胞的伤害程度加重。可见,高铵抑制拟南芥根系和地上部生长,高铵钾比则会加重这种抑制,其原因除了高浓度钾能减少植物对铵的吸收外,可能与高铵钾比条件加剧了植物的氧化胁迫有关。因此,适宜的铵钾比在植物应对铵毒害的过程中发挥重要作用。     

DEVELOPMENT OF A SOIL N TEST FOR FERTILIZER REQUIREMENTS FOR WHEAT

Optimal fertilizer nitrogen (N) rates result in economic yield levels and reduced pollution. A soil test for determining optimal fertilizer N rates for wheat has not been developed for Quebec, Canada, or many other parts of the world. Therefore, the objectives were to determine: 1) the relationship among soil nitrate (NO^? ₃)- N, soil ammonium (NH ⁺ ₄)- N and N fertilizer on wheat yields; and 2) the soil sampling times and depths most highly correlated with yield response to soil NO^? ₃-N and NH ⁺ ₄-N. In a three year research work, wet and dried soil samples of 0- to 30- and 30- to 60-cm depths from 20 wheat fields that received four rates of N fertilizer at seeding and postseeding (plants 15 cm tall) were analyzed for NH ⁺ ₄-N and NO^? ₃ -N using a quick-test (N-Trak) and a standard laboratory method. Wheat yield response to N fertilizer was limited, but strong to soil NO^? ₃-N.     

Transformations of chemically fixed liquid anhydrous ammonia by soil microorganisms

Summary The application of liquid anhydrous NH₃ to soil leads to chemical fixation of NH₃ by organic matter and of NH _inf4 ^sup+ by clay minerals. A laboratory study was conducted to ascertain the biological transformations of newly fixed liquid anhydrous ¹⁵NH₃ in a Drummer silty clay loam by incubation of the ¹⁵N-labelled soil with glucose for 0, 7, 30, and 90 days and by sequential extraction of organic-matter-fixed ¹⁵NH₃ with 0.15 M Na₄P₂O₇, 0.15 M KOH, 0.1 M NaOH, and acidified dimethyl sulfoxide. About 16% of the ¹⁵NH₃ injected was fixed, of which 52% was accounted for by clay fixation. The various humic fractions (fulvic acid, humic acid, and humin) were obtained, and the distribution patterns of the fixed ¹⁵NH₃-N in these fractions were compared. The potential availability of the fixed ¹⁵NH₃-N was also estimated. The percentage of the ¹⁵NH₃ recovered as organic-matter-fixed ¹⁵NH₃ decreased as the length of incubation increased (to 28% after 90 days); the decrease was attributed in part to an increase in the amount recovered as clay-fixed NH _inf4 ^sup+ (from 52 to 64%). Changes in the distribution of the organic-matter-fixed ¹⁵NH₃-N in the humic fractions included: (1) an increase in the relative amount of the fixed ¹⁵NH₃ as humic acid in both the Na₄P₂O₇ and KOH extracts, (2) an increase in the percentage of organic-matter-fixed ¹⁵NH₃-N in the fulvic acid fractions as high-molecular-weight components (determined by dialysis) or as generic fulvic acid (determined by sorption-desorption from XAD-8 resin), and (3) an increase in the percentage of the organic-matter-fixed ¹⁵NH₃ as humin. The potential availability of the organic-matter-fixed ¹⁵NH₃-N decreased as the length of the incubation increased, from 22 to 4% over the 90-day incubation period, and was correlated significantly (0.05 level) with Na₄P₂O₇-extractable N. These results suggest that organic-matter-fixed liquid anhydrous NH₃ is initially more labile than the native soil N but becomes less labile with time.     

土壤温度、水分和NH4+-N浓度对土壤硝化反应速度及N2O排放的影响

硝化反应是土壤、特别是干旱半干旱地区农业土壤N2O产生的重要途径之一。但是,目前环境条件对硝化反应中N2O排放的影响研究较少,而在国内外通用的几个模型中均用固定比例估算硝化反应过程中N2O的排放。本文通过砂壤土培养试验,研究了土壤温度、水分和NH4+-N浓度对硝化反应速度及硝化反应中N2O排放的影响,并用数学模型定量表示了各因素对硝化反应的作用,用最小二乘法最优拟合求得该土壤的最大硝化反应速度及N2O最大排放比例。结果表明,随着温度升高,硝化反应速度呈指数增长;水分含量由20%充水孔隙度(WFPS)增加到40%WFPS时,反应速度增加,水分含量增加到60%WFPS时反应速度略有降低;NH4+-N浓度增加对硝化反应速度起抑制作用。用米氏方程描述该土壤的硝化反应过程,其最大硝化反应速度为6.67mg·kg?1·d?1。硝化反应中N2O排放比例随温度升高而降低;随NH4+-N浓度增加而略有增加;20%和40%WFPS水分含量时,硝化反应中N2O排放比例为0.43%～1.50%,最小二乘法求得的最大比例为3.03%,60%WFPS时可能由于反硝化作用,N2O排放比例急剧增加,还需进一步研究水分对硝化反应中N2O排放的影响。