空间直观景观模型LANDIS在大兴安岭呼中林区的应用

应用空间直观景观模型 (L ANDIS) ,研究有采伐和无采伐预案下大兴安岭呼中林区的森林景观的长期变化。用 APACK计算每一个物种及各年龄级的分布面积。为了研究物种分布格局的变化 ,计算了物种分布的聚集度指数。研究结果如下 :(1)在无采伐预案下 ,火干扰模式为低频率大面积高强度火烧 ;在有采伐预下 ,火干扰模式为高频率小面积低强度火烧 ;(2 )在无采伐预案下 ,火会造成各种群分布面积的强烈波动 ,但是对种群的年龄结构没有很大影响 ;在有采伐预案下 ,火对种群分布面积和年龄结构都没有很大的影响 ;(3)采伐能完全改变各种群的年龄结构 ,降低种群分布的聚集度 ,但是对各种群的分布面积并没有很大影响 ;(4 )在有采伐预案下 ,各种群为增长型种群 ,增长量通过采伐取走 ,群落处于演替的干扰顶极状态 ;在无采伐预案下 ,各种群为稳定型种群 (樟子松和偃松除外 ) ,大面积高强度火烧使群落产生较大的波动。结果表明 ,在呼中林业局 ,在没有人为干扰情况下 ,火干扰是森林景观变化的主导因素。自从有了人为干扰 ,采伐开始逐渐取代火干扰成为影响森林景观变化的主导因素。空间直观景观模型的一个挑战是模型的验证。由于缺乏详细的空间数据及模型模拟中的随机性 ,很难通过模型模拟结果与实地调查或遥感数据的比较进行

免耕与常规耕作潮棕壤交换性阳离子的剖面分布特征

通过田间定位试验,研究了不同耕作方式对潮棕壤0-100 cm深度6个土层土壤交换性阳离子的影响。结果表明,与常规耕作相比,免耕使土壤表层pH显著增加,而电导率下降;同时,免耕增加了表层土壤可交换性K+含量,降低了可交换性Na+含量,但对可交换性Ca2+,Mg2+和阳离子交换量没有产生显著影响。相关分析结果表明,可交换性K+与土壤养分含量没有显著相关性,而可交换性Na+,Ca2+,Mg2+和阳离子交换量与有机质和全氮含量均呈负相关关系。

黄土高原旱地施肥对小麦与苜蓿土壤水分养分含量的影响

研究黄土高原旱地小麦(Wheat)和苜蓿(Alfalfa)连作20年后的产量、土壤水分及养分的变化。结果表明:磷肥对小麦增产不显著,而对苜蓿则增产显著(增产183.5%);施肥可以延缓苜蓿的衰老,提高产草量;苜蓿地土壤干燥化明显,施用氮磷有机肥后小麦地也出现干燥化趋势;长期施磷肥有利于改善土壤磷素有效性,其中苜蓿地全磷和有效磷含量,增加了13.6%和83.8%,小麦土壤增加了22.9%和367.9%;苜蓿土壤全氮和速效氮均呈增加,而小麦地则减少;平衡施用氮磷有机肥能培肥土壤,使产量大幅度提高;在该区采取合理的轮作方式和培肥措施能有效地改善农田生态系统的生产力。

渗灌——设施园艺先进的节水灌溉技术

渗灌具有降低室内湿度、改善土壤环境、节约灌溉用水、减少肥料用量、省工省时、价格适中等优点 ,是目前设施园艺先进的节水灌溉技术。详细介绍了渗灌系统的结构 ,渗灌管的种类以及使用维护方法。

西藏特有植物砂生槐天然居群遗传多样性研究

采用等位酶淀粉凝胶电泳技术对西藏雅鲁藏布江中游砂生槐 (Sophoramoorcroftiana) 10个天然居群的遗传多样性进行了研究。 13个酶系统 2 4个酶位点 ( 46个等位基因 )的检测结果表明 ,砂生槐具较低的遗传变异水平。居群水平上的遗传多样性指标分别为 :多态位点百分率Pp =2 5 .0 %～ 37.5 % ,等位基因平均数Ap=1.3～ 1.7,平均期望杂合度Hep=0 .112～ 0 .16 9;种水平上的遗传多样性 (Ps=37.5 % ,As=1.9,Hes=0 .171)低于长寿命木本被子植物的平均值 (Ps=5 9.5 % ,As=2 .10 ,Hes=0 .183)。居群遗传结构的分析显示 ,10个居群中随机交配的偏差为FIS=- 0 .0 0 71,表明砂生槐在居群水平上存在轻微的杂合子过量现象 ,偏离了Hardy Weinberg平衡 ;FST=0 .1748,表明砂生槐是居群间分化较大的一类多年生木本植物 ,主要原因是环境恶化和人类活动干扰 (过度砍伐、放牧等 )导致其生境片断化 ,从而影响了居群间基因交流而造成基因流水平较低 (Nm =1.180 2 )。砂生槐高海拔居群H2 (谢通门 )、H31(江当 1)、H32 (江当 2 )、H5 (朗塞岭 )包含着绝大部分等位基因 ,显示了相对较高的遗传多样性水平 ,应加以保护和管理 ,作为砂生槐种质资源就地保存的基地。

Investigation on the microstructure and mechanical properties of a cast Mg–6Zn–5Al–4RE alloy

Mg-6Zn-5Al-4RE (RE = Mischmetal, mass%) alloy was prepared by metal mould casting method. The microstructure and mechanical properties of the as-cast and heat-treated alloys were investigated

Self-assembly of lambda-DNA networks/Ag nanoparticles: Hybrid architecture and active-SERS substrate

In this article, highly rough and stable surface enhanced Raman scattering (SERS)-active substrates had been fabricated by a facile layer by-layer technique. Unique lambda-DNA networks and CTAB capped silver nanoparticles (AgNP) were alternatively self-assembled on the charged mica surface until a desirable number of bilayers were reached. The as-prepared hybrid architectures were characterized by UV-vis spectroscopy, tapping mode atomic force microscopy (AFM) and confocal Raman microscopy, respectively.

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.

Formation equilibria of ternary metal complexes with citric acid and glutamine (alanine) in aqueous solution

The species and their formation constants in the ternary, systems were obtained by the Scogs2 software from potentiometric titration data. The Comics software was used to calculate the distribution of species in the ternary systems. MLXH, MLXH2 and MLXH3 are the common species in these systems. The coordination behaviors of the rare earths are very similar and their stability is closely matched. The ternary rare earth complexes are more stable than the corresponding ternary complexes of calcium. The ternary zinc complex with glutamine as the secondary ligand is more stable than the corresponding complexes of rare earths, but the ternary complex with alanine as the secondary ligand shows an inverse trend. The distributions of species in the ternary systems vary with pH changing. A prediction can be made that exogenous rare earths can affect the species of Ca and Zn in human body.

Mass transfer kinetics of yttriium(III) using a constant interfacial cell with laminar flow. Part I. Extraction with Cyanex 302

The interfacial tension is measured for Cyanex 302 in heptane and adsorption parameters are calculated according to Gibbs equation and Szyskowski isotherm. The results indicate that Cyanex 302 has a high interfacial activity, allowing easy extraction reaction to take place at the liquid-liquid interface. The extraction kinetics of yttrium(III) with Cyanex 302 in heptane are investigated by a constant interfacial cell with laminar flow. The effects of stirring rate, temperature and specific interfacial area on the extraction rate are discussed. The results suggest that the extraction kinetics is a mixed regime with film diffusion and an aqueous one-step chemical reaction proposed to be the rate-controlling step. Assuming the mass transfer process can be formally treated as a pseudo-first-order reversible reaction with respect to the metal cation, the rate equation for the extraction reaction of yttrium(III) with Cyanex 302 at pH <5 is obtained as follows:R-f = 10(-7.85)[Y(OH)(2)(+)]((a))[H(2)A(2)]((o))(1.00)[H+]((a))(-1.00)Diffusion parameters and rate constants are calculated through approximate solutions of the flux equation.

Sol-gel fabrication, patterning and photoluminescent properties of LaPO4 : Ce3+, Tb3+ nanocrystalline thin films

Ce3+ and/or Tb3+-doped LaPO4 nanocrystalline thin films and their patterning were fabricated by a sol-gel process combined with soft lithography on silicon and quartz glass substrates. The results of XRD indicated that the films began to crystallize at 700 degreesC. The 1000 degreesC annealed single layer films are transparent by eyes, uniform and crack-free with a thickness of about 200 nm and an average grain size of 100 nm. Patterned thin film with different band widths (5-50 mum) were obtained by micro-molding in capillaries technique. The luminescence and energy transfer properties of Ce3+ and Tb3+ were studied in LaPO4 films.

Synthesis, characterization and fabrication on a glassy carbon electrode of a tetra-iron substituted sandwich-type pentadecatungstodiarsenate heteropolyanion

A novel sandwich-type compound, Na-12[Fe-4(H2O)(2)(As2W15O56)2].41H(2)O, has been synthesized. The compound was well-characterized by means of IR, UV-vis, W-183 NMR and elemental analyses. The compound crystallizes in the triclinic, P (1) over bar symmetry group. The structure of the compound is similar to that of Na-16[M-4(H2O)(2)(As2W15O56)(2)].nH(2)O (M = Cu, Zn, Co, Ni, Mn, Cd), and consists of an oxo-aqua tetranuclear iron core, [(Fe4O14)-O-III(H2O)(2)], sandwiched by two trivacant alpha-Wells-Dawson structural moieties, alpha-[As2W15O56]. Redoxelectrochemistry of the compound has been studied in buffer solutions at pH = 4.7 using polarography and cyclic voltammetry ( CV). The compound exhibited four one-electron couples associated with the Fe(III) center followed by three four-electron redox processes attributed to the tungsten-oxo framework. The compound-containing monolayer and multilayer films have been fabricated on a 4-aminobenzoic acid modified glassy carbon electrode surface by alternating deposition with a quaternized poly(4-vinylpyridine) partially complexed with [Os(bpy)(2)Cl](2+/-). CV, X-ray photoelectron spectroscopy (XPS), UV-vis spectroscopy and atomic force microscopy (AFM) have been used to characterize the multilayer films.

Study on the integrated membrane processes of dehumidification of compressed air and vapor permeation processes

Blend modified polyimide (PI) hollow fiber membranes were used in vapor permeation for gas phase dehydration of ethanol. Dry air sweeping operation was used and the dry air was supplied by a dehumidification membrane module of compressed air. An integrated membrane process was composed. The effects of some factors, such as the modification of membrane materials, the humidity and current velocity of sweeping air, the operation temperature, on the efficiency of dehydration were discussed.

Single-crystal X-ray structure and properties of K-10[Ni-4(H2O)(2)(AsW9O34)(2)]center dot 4H(2)O

The rational synthesis and the structural and magnetic characterization of a nickel cluster are presented. The compound comprises a rhomblike Ni4O16 group encapsulated between two-heptadentate tungstoarsenate ligands [AsW9O34](9-). The crystal structure of K-10[Ni-4(H2O)(2)(AsW9O34)(2)](.)4H(2)O was solved in monoclinic, P2(1)/n symmetry, with a = 12.258(3) Angstrom, b = 21.232(4) Angstrom, c = 15.837(3) Angstrom, beta = 92.05(3)degrees, V = 4119.1(14) Angstrom(3), Z = 2, and R = 0.0862. The crystal structure of the Ni(II) derivative was compared with that of the Cu(II), Zn(II), Co(II) and Mn(II) derivatives. The Ni4O14(H2O)(2) unit in the compound shows no Jahn-Teller distortion. On the other hand, the Ni(II) derivative shows ferromagnetic exchange interactions within the Ni4O16 group (J = 7.8 cm(-1), J' = 13.7 cm(-1)) and an S = 4 ground state, the highest spin state reported in a heteropoly complex. Its redox electrochemistry has been studied in acid buffer solutions using cyclic voltammetry. It exhibited two steps of one-electron redox waves attributed to redox processes of the tungsten-oxo framework. The new catalyst showed an electrocatalytic effect on the reduction of NO2-.

Advances in gas-phase electrophilic aromatic substitution reaction

Recent advances in the gas - phase reaction of aromatics with cationic electrophiles are reviewed. The overall substitution reaction is analyzed in terms of its elementary steps. Mechanistic studies have been focused on the structure and reactivity of covalent and non - covalent ionic intermediates, which display a rich chemistry and provide benchmark reactivity models. Particular attention has been devoted to proton transfer reactions, which may occur intra or intermolecularly in arenium intermediates.