不同施肥模式下潮棕壤稻田的速效养分状况和水稻的养分分配

研究了不同施肥模式下下辽河平原潮棕壤稻田土壤速效养分的供应能力及水稻的养分分配。结果表明:各处理0～20cm速效养分供应能力均高于20～40cm,其变异也大于20～40cm(速效氮除外);有机、无机肥相结合有利于提高土壤速效养分的供应能力;水稻氮和磷的分配主要集中在籽实中,钾的分配则主要集中在秸秆中。采用秸秆还田措施有利于缓解钾肥资源的不足,保持钾素的循环再利用,维持土壤钾库,减少钾肥投入,降低农业生产成本,减轻环境污染。

潮棕壤不同利用方式下植物线虫垂直分布研究(英文)

2003 年11 月,在中国科学院沈阳生态实验站潮棕壤经过不同利用方式后对水稻田、玉米地、撂荒地和林地开展了植物线虫垂直分布(0–15 cm 各土层)特征研究。研究结果表明:不同土地利用方式下的某些优势属线虫随着土壤深度增加而呈下降趋势。螺旋属(Helicotylenchus)线虫是4 种土地利用方式中最优势的属。水田丝尾属(Filenchus)、平滑属(Psilenchus)和垫刃属(Tylenchus)线虫主要分布在上层(0–20 cm),而撂荒地、林地中的针属(Paratylenchus)线虫及玉米地中的短体属(Pratylenchus)线虫能够分布在更深的土层(0–80 cm)。本研究揭示,植物线虫优势属数量与土壤化学特性指标存在显著相关关系。不同利用方式螺旋属线虫数量与土壤C/N 比、全碳、全氮、全磷、碱解氮及Olsen-P含量呈显著正相关;水田丝尾属和平滑属线虫、玉米地短体属线虫、撂荒地针属线虫与土壤pH 程显著负相关,与土壤全碳、全氮及碱解氮呈显著正相关。为了更正确地评价植物线虫种群数量,有必要根据植物线虫优势属的垂直分布特征来确定取样深度。图1 表1 参21。

宁夏黄土区不同植物群落土地利用方式对土壤质量的影响

本文研究了宁夏南部山区典型植物群落土地不同利用方式下土壤质量的变化。结果表明:(1)典型长芒草群落土地,开垦地比封禁地土壤有机质、全氮、全磷、速效氮、速效磷、速效钾养分含量明显降低,降低幅度分别为19.5%、20.1%、17.6%1、3.0%、77.8%和47.5%。脲酶活性为开垦地>封禁地,蔗糖酶则表现为封禁地>开垦地,中性磷酸酶差异不明显。(2)铁杆蒿群落土地三种利用方式下:放牧地土壤有机质、全氮、全磷、速效钾等养分含量较封禁地与开垦地有一定幅度的增加;放牧地的土壤脲酶、蔗糖酶和中性磷酸酶活性均高于封禁和开垦的同土层土壤,封禁地的脲酶和蔗糖酶次之,开垦地的脲酶和蔗糖酶活性最小,开垦地的中性磷酸酶活性高于封禁地。脲酶活性在土层之间变化较小,最高为放牧地表层177.6 mg/(kg.h),最低为开垦地表下层114.5 mg/(kg.h),蔗糖酶活性层次之间变化明显,其中放牧地表层为表下层的3倍左右。长芒草群落土壤表层各级微团聚体表现为封禁地远大于开垦地,铁杆蒿群落土地不同利用方式下各级微团聚体表现不同,结构系数表现为表层>表下层,保持率则为表层<表下层。结构系数与保持率均表现为封禁地>放牧地>开垦地。(3)在...

土壤有机质对土霉素在土壤中吸附-解吸的影响

采用批量平衡方法,研究了土霉素在原土及去除有机质土壤中的吸附和解吸.结果表明,土霉素在原土和去除有机质土壤中的吸附和解吸等温线均不同程度地偏离线性模型,其中Freundlich模型可以对吸附和解吸数据进行良好的非线性拟合,在不同土壤以及不同土壤处理中的拟合相关系数(r)均达到极显著水平.去除有机质能够降低土霉素在土壤中的吸附容量(lgKf),但增加了吸附强度(1/n).土霉素在土壤上的解吸过程存在明显的滞后现象,在所设土霉素浓度范围内,土霉素在褐土和红壤中的平均滞后系数(HIa)分别为0.039和0.015;去除有机质后的褐土和红壤对土霉素的解吸滞后现象显著增强(P<0.01),其HIa分别增加到0.068和0.028.

Relationships between precipitation, soil water and groundwater at Chongling catchment with the typical vegetation cover in the Taihang mountainous region, China

Vegetation cover plays an important role in the process of evaporation and infiltration. To explore the relationships between precipitation, soil water and groundwater in Taihang mountainous region, China, precipitation, soil water and water table were observed from 2004 to 2006, and precipitation, soil water and groundwater were sampled in 2004 and 2005 for oxygen-18 and deuterium analysis at Chongling catchment. The soil water was sampled at three sites covered by grass (Carex humilis and Carex lanceolata), acacia and arborvitae respectively. Precipitation is mainly concentrated in rainy seasons and has no significant spatial variance in study area. The stable isotopic compositions are enriched in precipitation and soil water due to the evaporation. The analysis of soil water potential and isotopic profiles shows that evaporation of soil water under arborvitae cover is weaker than under grass and acacia, while soil water evaporation under grass and acacia showed no significant difference. Both delta O-18 profiles and soil water potential dynamics reveal that the soil under acacia allows the most rapid infiltration rate, which may be related to preferential flow. In the process of infiltration after a rainstorm, antecedent water still takes up over 30% of water in the topsoil. The soil water between depths of 0-115 cm under grass has a residence time of about 20 days in the rainy season. Groundwater recharge from precipitation mainly occurs in the rainy season, especially when rainstorms or successive heavy rain events happen.

A topography/chemical composition gradient polystyrene surface: Toward the investigation of the relationship between surface wettability and surface structure and chemical composition

In this paper, we have prepared of a topography/chemical composition gradient polystyrene (PS) surface, i.e., an orthogonal gradient surface, to investigate the relationship between surface wettability and surface structure and chemical composition. The prepared surface shows a one-dimensional gradient in wettability in the x, y, and diagonal directions, including hydrophobic to hydrophilic, superhydrophobic to hydrophobic, superhydrophobic to superhydrophilic gradients, and so forth.

Synthesis, photophysical properties, and theoretical studies on pyrrole-containing bromo Re(I) complex

Two bromo rhenium(I) carbonyl complexes with the formula of [Re(CO)(3)(L)Br], where L = 1,10-phenanthroline (Phen-Re) and 5-(1H-pyrrol-1-yl)-1,10-phenanthroline (Pyph-Re), were successfully synthesized with the aim to analyze the effect of the pyrrole (Py) moiety on the photophysical properties of Pyph-Re. It was found that the triplet metal-to-ligand charge-transfer d pi (Re) --> pi*(N-N) emission of Phen-Re and Pyph-Re centered at ca. 527 nm with the luminescence quantum yield (LQY) of 0.015 and ca. 578 nm with the LQY of 0.011, respectively. At the same time, the geometrical structures of the ground state and the absorption spectral properties of Phen-Re and Pyph-Re were also calculated with the 6-31G* basis set employed on C, H, N, O, and Br atoms, and LANL2DZ adopted on Re atom.

Free radical grafting of polyethylene with vinyl monomers by reactive extrusion

The free radical grafting of polyethylene with vinyl monomers by reactive extrusion was studied numerically. Numerical computation expressions of key variables, such as the concentrations of the initiator and polymer, grafting degree, average molecular weight and apparent viscosity, were deduced. The evolutions of the above variables were predicted by means of an uncoupled semi-implicit iterative algorithm. The monomer conversion monotonically increases with decreasing throughput or increasing initial initiator concentration; with increasing barrel temperature, the monomer conversion first increases then decreases. The simulated results are nearly in good agreement with the experimental results.

Modification of electrode surface through electrospinning followed by self-assembly multilayer film of polyoxometalate and its photochromic

Electrospun poly (vinyl alcohol) (PVA) nanofibers mat was collected on indium tin oxide (ITO) substrate. Heat crosslinked nanofibers mat became water-insoluble and firmly fixed on ITO substrate even in water. Oppositely charged poly (allylamine hydrochloride) (PAH) and Dawson-type polyoxometalate (POM), Na6P2Mo18O62 (P2Mo18), were alternately assembled on PVA nanofibers-coated ITO substrate to construct multilayer film through an electrostatic layer-by-layer (LBL) technique. The scanning electron microscope (SEM) images showed that P2Mo18 multilayer film was selectively deposited on PVA nanofibers while the unoccupied space by nanofibers on bare ITO was acted as substrate at the same time because the electrospun nanofibers have larger surface area and surface energy than the flat substrate. The cyclic voltammograms current responses of the P2Mo18 multilayer film on PVA/ITO electrode showed three well-defined redox couples of P2Mo18, but very small because P2Mo18 multilayer film was selectively deposited on PVA nanofibers with poor conductivity. In addition, the photochromic behavior of P2Mo18 multilayer film on PVA/ITO was investigated through UV-vis spectra and electron spin resonance (ESR). Fourier-transform infrared (FT-IR) spectroscopy and X-ray photoelectron spectroscopy (XPS) proved that the charge-transfer complex was formed between PAH and P2Mo18 after UV irradiation.

Synthesis and crystal structure of the dimeric, Ti-O-Ti bridged hydrid form polyoxoanion [alpha-1, 2-PW10Ti2O39](2)(10-)

The reaction of trivacant precursor Nag [A-PW9O34] . 19H(2)O with Ti(SO4)(2) affords the novel dimeric, di-Ti-IV-substituted tungstophosphate K4Na6[alpha-1,2-PW10Ti2O39](2) . 14H(2)O. The X-ray structural determination shows the dimeric, anhydride structure was formed by two Ti-O-Ti bonds linking two di-titanium-substituted Keggin anion [alpha-1,2-PW10Ti2O40]. It was also characterized by elemental analysis, TGA, FT-IR and U-V-vis spectroscopies.

Electrocatalytic oxidation of NADH by rutin in biomembrane-like films on glassy carbon electrode

Stable lipid film was made by casting dipalmitoylphosphatidylcholine (DPPC) and rutin onto the surface of a glassy carbon (GC) electrode. The electrochemical behavior of rutin in the DPPC film was studied. The modified electrode coated with rutin gave quasi-reversible reduction-oxidation peak on cyclic voltammogram in the phosphate buffer (pH 7.4). The peak current did not decrease apparently after stored at 4 degreesC for 8 hours in refrigerator. This model of biological membrane was used to investigate the oxidation of dihydronicotinamide adenine dinucleotide (NADH) by rutin. Rutin in the film acts as a mediator. The modified electrode shows a great enhancement and the anodic peak potential was reduced by about 220 mV in the oxidation of 5 X 10(-3) mol L-1 NADN compared with that obtained at a bare glassy carbon electrode. (C) 2000 Elsevier Science S.A. All rights reserved.

Chiral separation of promethazine by capillary electrophoresis with end-column amperometric detection

Sensitive end-column amperometric detection has been successfully coupled to capillary electrophoresis for chiral separation of promethazine, with a carbon fiber microdisk electrode as working electrode. Baseline separation and sensitive detection were achieved under optimum conditions: 0.030 M Na2HPO4 and 0.015 M citric acid at pH = 2.50, 1.0 mM beta -CD, 10 kV separation voltage, and detection potential 1.10 V (vs Ag/AgCl). The numbers of theoretical plates were higher than 700000, and the detection limit was 5 x 10(-8) M. On-line treatment of the electrode has also been studied and discussed.

Separation of promethazine and thioridazine using capillary electrophoresis with end-column amperometric detection

Promethazine and thioridazine were separated and detected by capillary electrophoresis with end-column amperometric detection. The influence of pH Value on oxidation potential, the peak current and the resolution were studied and the following conditions was selected: 0.03 M Na2HPO4 and 0.015 M citric acid at pH 3.0, detection potential at 1.10 V. The detection limits of these two substances were in the range of 10(-8) mol/l. The linear range spanned two to three orders of magnitude. This method was applied to the detection of promethazine and thioridazine spiked in urine. (C) 1999 Elsevier Science B.V. All rights reserved.