缓释尿素氮肥在玉米苗期的养分释放特点

采用盆栽试验,模拟田间生态环境,研究施用不同种缓释氮素肥料玉米苗期土壤的尿素态氮、硝态氮和铵态氮含量。结果表明,施用硝化和脲酶抑制剂(DCD/NPBT)涂层尿素肥料的尿素态氮含量最高,为14.37mg/kg,延缓尿素转化效果明显;施用醋酸酯淀粉包膜尿素肥料,硝态氮含量最高,为102.08 mg/kg。2种膜材料包膜硝化抑制剂(DCD)涂层尿素、包膜DCD/NPBT涂层尿素肥料的铵态氮含量都很高,在56.38~60.22 mg/kg之间,而硝态氮含量都很低,DCD/NPBT涂层尿素肥料的硝态氮含量也很低,在28.0 mg/kg左右。包膜抑制剂涂层尿素肥料对氮素养分的缓释效果优于只包膜尿素,包膜涂层2种抑制剂优于一种抑制剂,涂层2种抑制剂优于只涂层一种抑制剂;丙烯酸树脂包膜肥料的缓释性能强于醋酸酯淀粉包膜。

科尔沁沙地22种菊科草本植物叶片形态特征研究

以内蒙古科尔沁沙地22种菊科草本植物为实验材料,研究这些植物的比叶面积、叶片厚度、叶片干物质含量、叶片体积、叶重比和叶片组织密度等特性之间的关系。结果表明,叶片体积和叶片厚度之间存在较强的正相关,其相关系数r=0.782。而叶片厚度与叶片组织密度、比叶面积与叶片组织密度、叶片体积与叶片组织密度之间则存在一定的负相关性,它们的相关系数分别为-0.767、-0.559和-0.505,其余各特性之间均不存在相关性。根据赋值后数据或者二元数据,运用聚类分析方法得出3个组群,并运用单因素方差分析方法检验各特性在各组间的显著性,叶片厚度、叶片体积、叶重比和叶片组织密度特性在组间存在极显著差异。

冬小麦播种密度和施肥方式对麦田杂草群落组成及生长的影响

在半湿润地区的土垫旱耕人为土上,以冬小麦品种小偃22为指示作物,通过田间小区试验研究了不同施肥条件下冬小麦田间杂草种群的组成以及在4个生育期(越冬期、返青期、拔节期、成熟期)田间杂草密度和生物量的变化.结果表明:(1)在冬小麦全生育期内共发现以猪殃殃、麦家公、婆婆纳、播娘蒿、泽漆、荠菜等为主的17种杂草,不同生育期杂草的优势种群不同,而且杂草总密度表现为越冬期>返青期>拔节期,生物量表现为拔节期>返青期>越冬期;(2)与不施肥处理(P0N0)比较,单施氮肥增加了杂草密度和生物量,在氮磷配施条件下,氮肥对生物量有极显著影响且随施氮量增加表现为减小趋势,其中PN45处理的杂草生物量最大并比P0N0增加51.8%;施磷对杂草生物量有极显著影响,其中单施磷比P0N0处理增加44.0%,PN135处理比P0N135处理增加24.0%.(3)低密度播种比正常密度播种能显著增加杂草生物量,平均增加幅度达82.9%.结果表明,通过增施氮肥和适当增加种植密度,可在一定程度上控制杂草发生,促进作物良好生长

土壤养分对小偃22叶片光合特性影响的初步研究

在大田不同供肥条件下 ,于小麦灌浆后期对小麦旗叶光合特性参数进行了连续测定。结果表明 ,小麦叶片气体交换参数均有明显的日变化趋势 ,肥力条件对其日变化进程具有明显的调控作用。不施肥处理小麦叶片 Pn有明显午休现象 ,而低肥处理第一高峰不明显 ,没有明显午休现象 ;高肥处理的 Pn呈单峰曲线 ,峰值来得也较晚。养分条件可改善小麦叶片水分利用效率

榆耳有性结构及生活史的研究

本文通过电镜扫描、石腊切片及用苏木精染色法和DAPI荧光染色,对榆耳子实体有性结构进行观察,证实榆耳子实体菌盖结构分三层:上表层为毛层,表面着生有排列较密集顶端游离的菌丝,它们相互粘连呈菌丝束;中间层为髓部,由较疏松而相互交织在一起的薄壁菌丝组成,菌丝间充满胶质物质;下表层为子实层,表面起伏不平,呈不规则的疣状突起,上面着生担子和囊状体,担子无隔膜棍棒形,外表有不规则的网状纹饰,其顶部着生4个瓶梗状小梗,每个小梗上着生1个椭圆形或腊肠形担孢子,大小为2.5—3.0×6.0—6.5μm,担孢子表面有不规则的网状纹饰结构。在担子间的囊状体为长圆柱形或圆锥形,表面有较密的不规则的网状纹饰。 榆耳有性生殖为异宗配合。绝大多数担孢子含一个细胞核,很少数担孢子含两个细胞核。孢子萌发为一端萌发,也有少数为两端萌发。初生菌丝单核,不能形成子实体,当两种不同遗传性的交配型的初生菌丝结合后,形成具有锁状联合结构的双核菌丝,并可发育成子实体。榆耳具有典型减数分裂过程,不具有减数分裂后核分裂行为,四个子核分别进入四个担孢子内。 在初生菌丝或次生菌丝上,均可产生间生的或顶生的厚垣孢子。经过温度、光照和紫外线照射的诱发,均未发现有其它类型的无性孢子产生。因此,榆耳菌的生活史和大多数担子

Determination of atenolol and metoprolol by capillary electrophoresis with Tris(2,2 '-bipyridyl)ruthenium(II) electrochemiluminescence detection

Capillary electrophoresis (CE) coupling with a tris(2,2'-bipyridyl)ruthenium(II) (Ru(bpy)(3)(2+)) electrochemiluminescence (ECL) detection technique was developed for the analysis of two 8-blockers, atenolol (AT) and metoprolol (ME). The parameters that influence the separation and detection, including the buffer pH and concentration, the separation voltage, the detection potential and Ru(bpy)(3)(2+) concentration, were optimized in detail. The calibration curve was linear over a concentration range of two or three orders of magnitude for the two beta-blockers. The detection limits for AT and ME were 0.075 and 0.005 mu M (S/N = 3). The relative standard deviations (n = 8) of the ECL intensity and the migration time were 2.65 and 0.22% for AT, 2.82 and 0.34% for ME, respectively. The proposed method was applied to determine AT and ME in spiked urine samples; satisfactory results were obtained.

Synthesis, structural and electrical characterizations of Sr2Fe1-xMxNbO6 (M = Zn and Cu) with double perovskite structure

Sr2Fe1-xZnxNbO6-x/2 (0 <= x <= 0.5) and Sr2Fe1-xCuxNbO6-x/2 (0.01 <= x <= 0.05) with the double perovskite structure have been synthesized. The crystal structures at room temperature were determined from Rietveld refinements of X-ray powder diffraction data. The plots of the imaginary parts of the impedance spectrum, Z '', and the electric modulus, M '', versus log (frequency), possess maxima for both curves separated by less than a half decade in frequency with associated capacities of 2 nF. The enhancement of the overall conductivity Of Sr2Fe1-xMxNbO6-x/2 (M = Cu and Zn) is observed, as increases from 2.48 (3) x 10(-4) S/cm for Sr2FeNbO6 to 3.82 (5) x 10(-3) S/cm for Sr2Fe0.8Zn0.2NbO5.9 at 673 K. Sr2Fe0.8Zn0.2NbO5.9 is chemically stable under the oxygen partial pressure from 1 atm to 10(-22) atm at 873 K. The p and n-type electronic conductions are dominant under oxidizing and reducing conditions, respectively, suggesting a small-polaron hopping mechanism of electronic conduction.

Bottom-contact organic field-effect transistors having low-dielectric layer under source and drain electrodes

An organic thin-film transistor (OTFT) having a low-dielectric polymer layer between gate insulator and source/drain electrodes is investigated. Copper phthalocyanine (CuPc), a well-known organic semiconductor, is used as an active layer to test performance of the device. Compared with bottom-contact devices, leakage current is reduced by roughly one order of magnitude, and on-state current is enhanced by almost one order of magnitude. The performance of the device is almost the same as that of a top-contact device. The low-dielectric polymer may play two roles to improve OTFT performance. One is that this structure influences electric-field distribution between source/drain electrodes and semiconductor and enhances charge injection. The other is that the polymer influences growth behavior of CuPc thin films and enhances physical connection between source/drain electrodes and semiconductor channel. Advantages of the OTFT having bottom-contact structure make it useful for integrated plastic electronic devices.

Excimer formation in uniaxially stretched polymer films

The steady-state fluorescence properties of naphthalene-labeled polymers dispersed in poly(methyl methacrylate) (PMMA) cast films were studied under tensile loadings at 80 degreesC. The labeled polymers were composed of methyl methacrylate (MMA) and 1-naphthylmethyl methacrylate (NMMA). Three of the copolymers were used in this work, and the contents of NMMA were 0.59 mol % (CP1), 22.0 mol % (CP2), and 56.7 mol % (CP3), respectively. The fluorescence spectra of the films containing CP1 and CP2were unchanged during elongation. For the film containing CP3, the excited monomer emission of naphthyl groups at around 337 nm decreased with increasing applied tensile strain. The strain enhanced the emission ascribed to the excimer of the naphthyl groups in the region of 390-420 nm. The ratio of fluorescence intensities at 400 nm and 337 mn, I-400/I-337, increased with the applied strain, which indicates that CP3 is a sensitive probe for detecting the structural changes of polymer matrices. The obtained results mean that the excimer-forming sites in the PMMA films during elongation depend both on the applied strain and the concentration of naphthyl groups in the dispersed polymer probes. (C) 2001 John Wiley & Sons, Inc.

Sol-gel synthesis and properties of Ce1-xGdxO2-x/2 solid solutions

A series of solid electrolytes Ce1-xGdxO2-x/2(x=0 similar to0.6) was prepared by sol-gel method. The structure, thermal expansion coefficient and electrical properties of the solid solutions were systematically studied. XRD data showed that a complete cubic fluorite structure was formed at 160 degreesC. The purity of the product prepared by the sol-gel method is higher, the grain size is uniformly smaller. They were easily sintered into highly dense ceramic pellets at 1 300 degreesC. The sintering temperature was significantly lower than that by traditionally high temperature solid phase reaction method. The thermal expansion coefficient of Ce0.8Gd0.2O1.9, determined from high- temperature XRD data, is 8. 125 X 10(-6) K-1. Impedance spectra analyses showed that the grain-boundary resistance of the solid electrolyte prepared by sol-gel method was reduced or even eliminated. The conductivity of Ce0.8Gd0.2O1.9 is 5.26 X 10(-3) S/cm at 600 degreesC. The activation energy (E-a) is 0.82 eV.

Synthesis and crystal structure of a novel amino-acid-containing polyoxometalate: K-6[Cu (Ala)(2) (H2O)(2)](2)[ CU4 (H2O)(2) (AsW9O34)(2)] center dot 16H(2)O

The novel amino-acid-containing polyoxometalate Ka(6) [Cu(Ala)(2) (H2O)(2)](2) [Cu-4 (H2O)(2) . (AsW9O34)(2)] . 16H(2)O was synthesized from the reaction of K-10[Cu-4(H2O)(2)(AsW9O34)(2)] . 20H(2)O with beta -alanine, Its structure has been determined by single crystal X-ray diffraction. It crystallizes in the triclinic space group P (1) over bar, with a=1. 196 3(2) nm, b=1. 536 5(3) nm, c=1. 591 4(3) nm, alpha =93. 97(3)degrees, beta= 110. 88(3)degrees, gamma =101. 07(3)degrees, V=2. 651 8(9) nm(3) and Z=1. Least-squares refinement of the structure leads to R and R-w factors of 0. 067 3 and 0. 162 8, respectively. An unusual structural feature of the compound is that the polyanion [Cu-4(H2O)(2) (AsW9O34)](10-) is linked with the amino-acid complex of Cu2+ by a mu -oxygen atom.

Mass spectrometric studies of metallofullerene

The endrohel metallofullerene, Gd@C-82, Gd@C-80, Gd-2@C-80 were synthesized by using K-H method. The technique of two-step of high pressure and high temperature extraction with 1, 3, 5-trimethylbenzene (first step) and pyridine(second step) has been successfully utilized to extract metallofullerene of Gd@C-82 The gas-phase negative ions of fullerenes C-n(n= 60, 70, 78, 82, 84...) and metallofullerene (Gd@C-82) have been studied by the ESI-MS, REC-MS and MALDI-TOF-MS. The differences among the mass spectra of ESI-MS, REC-MS and MALDI-TOF-MS have been observed and explained. In contrast to the empty fullerene C-82 , the metallofullerene Gd@C-82 should have a larger HOMO-LUMO gap. Experimental results suggest that Gd@C-82 is polarized and Gd3+ located in the off-center position of C-82 cage after Gd3+ is trapped into C-82 cage.

金属富勒烯的质谱研究

利用电弧放电法合成笼内金属富勒烯 Gd@C82 ,Gd2 @C80 ,Gd@C80 .实验结果表明 ,两步高温高压法( 1 ,2 ,4 -三甲基苯 ,吡啶 )可有效地提取金属富勒烯 Gd@C82 .本文分别利用 ESI-MS,REC-MS,MALDI-TOF-MS质谱技术研究了 Gd@C82 ,Gd2 @C80 ,Gd@C80 和富勒烯 Cn( n=60 ,70 ,82 ,84… )的气相负离子特性 .结果表明 ,包入 Gd3 + 后非极性的 C82 转变为极性的 Gd@C82 分子 ;金属离子 Gd3 + 处于 C3 -82 笼中非中心的位置 .