土壤氧化还原酶催化动力学研究进展

土壤氧化还原酶是存在于土壤中的一种重要酶类,参与土壤中为数众多的重要生物化学反应,与土壤中有机物质的转化、腐殖质的形成以及土壤肥力变化密切相关.其催化反应的动力学研究常用来阐明其催化过程的特性、酶的本质属性及其对环境变化的响应等.研究土壤氧化还原酶动力学特征对探讨其来源、性质及影响因素,对进一步调控多种营养元素参与的反应过程有重要意义.文中概述了土壤氧化还原酶动力学研究的理论基础,综述了土壤氧化还原酶催化动力学研究的进展和影响因素,并对今后的研究提出了几点建议.

小叶白蜡接种外生菌根真菌对土壤石油烃的降解效果

采用盆栽实验研究了小叶白蜡(Fraxinus sogdiana)接种4种外生菌根真菌(E1-毛边滑锈伞(Hebeloma mesophaeusm)、E2-劣味乳菇(Lactarius insulsns)、E3-松塔牛肝菌(Stro-bilomyces floccopus)和E4-丝膜菌(Cortinarius russus)对沈抚灌区土壤石油烃的降解效果。结果表明:在白蜡不同组合双接种及混合接种中,以混合接种对土壤石油烃的降解效果最好,降解率比对照提高23.6%;其次为双接种中的E1E3和E2E4组合,降解率分别比对照提高21.0%和12.7%。接种外生菌根真菌可促进白蜡生长,尤其可明显提高其根生物量,增加侧根数,接种E1E3、E2E4和混合菌使白蜡侧根数分别增加了100%、67%和81%。相关分析表明,石油烃降解率与白蜡的侧根数呈显著相关,可能是其降解率提高的主要原因。

干旱区绿洲土地利用与覆被变化过程

应用遥感和GIS技术及数理统计学方法,以新疆三工河流域冲洪积扇-冲积平原型绿洲为研究区,利用1978年、1987年和1998年的遥感数据,深入研究了70年代中后期以来干旱区绿洲LUCC的过程和趋势。结果表明:(1)遥感和GIS在绿洲土地利用与覆被变化数据获取和空间分析方面是一种非常强大而有效的技术手段;(2)通过建立绿洲LUCC的幅度、速度、区域差异和变化趋势数学模型,可以较好的研究绿洲土地LUCC的过程和趋势,如变化的双向性、单向性、正向性和反向性,变化的涨势或落势等,在三工河流域绿洲应用取得良好效果;

干旱区绿洲景观尺度稳定性初步分析

在景观尺度上,从绿洲景观多样性、景观廊道的复杂性以及土地利用及其生态环境效应等方面探讨了绿洲景观稳定性的内涵,并对新疆三工河流域绿洲进行实例分析和应用。结果表明(1)人工绿洲景观的稳定需要绿洲景观的多样性逐渐降低和景观廊道的复杂性增加;但天然绿洲的稳定需要增加景观的多样性和景观廊道的复杂性。(2)人工绿洲景观稳定性还可从绿洲土地利用变化方面分析,绿洲土地利用变化是人类投入大量负熵的结果,投入的负熵越多,绿洲土地利用程度越高,越有利于绿洲从低级的亚稳定状态不断向高级稳定态发展,从而实现绿洲可持续发展。但人类

区域尺度绿洲稳定性评价

论文在区域尺度上,探讨了绿洲稳定性的内涵,并以新疆三工河流域绿洲为例,从绿洲所处的地理位置、绿洲与外围荒漠和山地系统之间的相互作用等方面评价了绿洲的区域稳定性。结果表明:①冲洪积扇型绿洲稳定性最高,其次是位于地下水溢出带下方的冲积平原型绿洲,稳定性最差的是湖滨三角洲或散流干三角洲上发育的绿洲;②绿洲的冷岛效应和植被指数可较好地表征绿洲与外围荒漠和山地系统之间的相互作用和评价绿洲的区域稳定性的时间变化。绿洲规模的扩大及绿洲水分和植被的增加将加强绿洲的冷岛效应,提高绿洲的稳定性;归一化差异植被指数增加,表明绿

中国云南轿子雪山自然保护区昆虫资源与生物多样性调查及齿颚卷象科Byctiscini族分类研究（鞘翅目，齿颚卷象科

本论文由两个单元组成，第一部分主要对中国云南轿子雪山自然保护区的昆虫资源分布、物种组成及生物多样性变化做了系统的研究探讨。第二部分是对中国齿颚卷叶象甲科(Rhynchitidae)的绿卷象族的分类系统及生物学进行了初步探讨。轿子雪山是距离昆明最近的自然保护区，并是少数著名的低纬度高海拔雪山之一。轿子雪山自然保护区的生态平衡影响着整个昆明地区的生态环境。但是对于此保护区的生物资源及多样性方面研究至今仍缺乏。作者于2006年8月至2007年8月对云南轿子雪山自然保护区昆虫资源进行了进一步摸底调查，并以地表甲虫为主要研究对象对其物种组成及生物多样性季节变化进行了连续跟踪调查。调查结果如下：1，共获得昆虫标本3725头，分别隶属于14目76科385种。经物种鉴定及对记录资料的进一步整理，得到轿子雪山自然保护区昆虫名录12目72科327种。2，通过对4种典型微环境样地(草地、灌丛、林地以及农田生态系统）的三次跟踪连续调查，共获得标本2451头，分别隶属于24科。其中步甲科(Carabidae)为优势类群，占总数的62.10%；隐翅虫科(Staphylinidae)其次，占12.77% 。可能由于海拔、气温等因素影响，该地区昆虫活动高峰期较短。3，通过对4种典型微生态环境中地表甲虫的生物多样性的比较，表明不同生境内甲虫的多样性指数存在动态变化，在不同生境片区内甲虫存在迁移活动，甲虫多在灌丛中越冬，并随季节及食物源迁移。卷叶象甲绿卷象族(Byctiscini)隶属于鞘翅目(Coleoptera)齿颚卷象科(Rhynchitidae)。以其独特的繁育后代方式——筑造多叶摇篮而闻名。其主要危害杨、苹果、梨、桦、盐肤木等许多重要经济树木。本文根据对文献资料的归纳整理和对现有昆虫标本的检视，对中国齿鄂卷象科(Rhynchitidae)的绿卷象族昆虫进行了较详细的分类系统学研究。共记述了绿卷象族卷叶象甲5属(Byctiscus、Aspidobyctiscus、Byctiscidius、Listrobyctiscus、Baikovius)43种，其中包括1中国新纪录种(Byctiscu regularis)。作者对本族昆虫的生物学及地理分布做了概括性描述，结果显示此族昆虫以东洋区为多数(48.84%)，古北区其次(34.88%)，东洋-古北共有种则占9.30%。此外，根据文献记述及标本检视，纠正一处物种记录错误，并针对部分物种编写了检索表。

Highly efficient red electroluminescent polymers with dopant/host system and molecular dispersion feature: polyfluorene as the host and 2,1,3-benzothiadiazole derivatives as the red dopant

By selecting polyfluorene as the polymer host, choosing 2,1,3-benzothiadiazole derivative moieties as the red dopant units and covalently attaching 0.3 mol% of the dopant units to the side chain of the polymer host, we developed a novel series of red electroluminescent polymers of dopant/host system with molecular dispersion feature. Their EL spectra exhibited predominant red emission from the dopant units because of the energy transfer and charge trapping from the polymer backbone to the dopant units. The emission wavelength of the polymers could be tuned by modifying the chemical structures of the dopant units.

Studies on alkaloids binding to GC-rich human survivin promoter DNA using positive and negative ion electrospray ionization mass spectrometry

Electrospray ionization mass spectrometry (ESI-MS) was used to investigate the binding of 13 alkaloids to two GC-rich DNA duplexes which are critical sequences in human survivin promoter. Negative ion ESI-MS was first applied to screen the binding of the alkaloids to the duplexes. Six alkaloids (including berberine, jatrorrhizine, palmatine, reserpine, berbamine, and tetrandrine) show complexation with the target DNA sequences. Relative binding affinities were estimated from the negative ion ESI data, and the alkaloids show a binding preference to the duplex with higher GC content. Positive ion ESI mass spectra of the complexes were also recorded and compared with those obtained in negative ion mode.

Structure characterization and physical properties of a complex with supramolecular architectures Co-2(2,6-DPC2Co(H2O)5 center dot 2H(2)O (DPC=2,6-pyridinedicarboxylate)

Reaction of 2,6-pyridinedicarboxylic with CoCl2 . 6H(2)O in aqueous solution give rise to a three-dimensional Complex CO2(2,6-DPC)(2)Co(H2O)(5).2H(2)O (DPC = 2,6-pyridinedicarboxylate) 1. It has been characterized by elemental analyses, infrared spectra (IR) spectrum, thermogravimetric (TG) analysis, EPR spectrum, and single crystal X-ray diffraction. The complex crystallizes in the P2(1)/c space group with a = 8.3906(3) Angstrom, b = 27.4005(8) Angstrom, c = 9.6192(4) A, alpha = 90.00degrees, beta = 98.327(2)degrees, gamma = 90.00degrees, V = 2188.20(14) Angstrom(3), Z = 4. There are two types of cobalt environments: Co(1) is coordinated by four oxygen atoms from four carboxyl groups and two nitrogen 2 atoms which are all from pdc(2). Co(2) is coordinated by six oxygen atoms, five from coordinated water molecules and one from a carboxyl of pdc(2) - of which the other oxygen atom is linked to the Co(1). The extensive intermolecular hydrogen bonds are formed in the crystal by means of the five coordinated water molecules.

A Monte Carlo simulation for the micellization of ABC 3-miktoarm star terpolymers in a selective solvent

We have used Monte Carlo simulation to study the micellization of ABC 3-miktoarm star terpolymers in a selective solvent (good to A segment, bad to B and C segments). The simulation results reveal that the self-assembled morphology is determined by the block length, molecular architecture, terpolymer concentration and insolubility of insoluble block in the solvent. In dilute solution, symmetric terpolymers (N-B = N-C = 30) tend to aggregate into a novel wormlike pearl-necklace structure linked by an alternating arrangement of B and C spheres, whereas the asymmetric terpolymers (NB = 10, NC = 50) are likely to aggregate into spherical or cylindrical micelles (formed by C blocks) connected with some small B spheres, when the concentration of terpolymer is relatively low (chain number is 100). However, when the concentration of terpolymer is relatively high (chain number is 250), the symmetric terpolymers tend to aggregate into a netlike structure linked by an alternation of B and C spheres, whereas the asymmetric terpolymers are likely to aggregate into wormlike micelles (formed by C blocks) connected with some of small spheres (formed by B blocks). Moreover, when the insolubility of insoluble block in the solvent is weak, the insoluble blocks aggregate into some incompact micelles.

Ti_(0.17)Zr_(0.08)V_(0.34)Nb_(0.01)Cr_(0.1)Ni_(0.3)氢化物电极合金微观结构及电化学性能研究

采用XRD、FESEM-EDS、ICP及EIS等方法研究了Ti0.17Zr0.08V0.34Nb0.01Cr0.1Ni0.3氢化物电极合金微观结构和电化学性能。X射线衍射分析表明:该合金由体心立方结构(bcc)的V基固溶体主相和少量六方结构的C14型Laves相组成;FESEM及EDS分析表明:V基固溶体主相形成树枝晶,C14型Laves相呈网格状围绕着树枝晶的晶界,元素在两相中的分布呈现镜像关系。电化学性能测试结果表明:该合金的氢化物电极在303￣343K较宽的温度区间内,表现出较高的电化学容量,在303K和343K时,电化学容量分别为337.0mAh·g-1和327.9mAh·g-1。在303K循环100周后,容量为282.7mAh·g-1。ICP分析结果表明,氢化物电极在充放电循环过程中,V及Zr元素向KOH电解质中的溶出较为严重。EIS研究表明,金属氢化物电极表面电化学反应的电荷转移电阻(RT)随循环次数的增加而增加,相应的交换电流密度则随循环次数的增加而降低。氢化物电极循环过程中RT的增大以及V和Zr元素的溶解,可能是导致电极容量衰减的主要原因。

Synthesis and structure of molybdenum-citrato cluster mu(2)-S bridge

A new molybdenum-citrato cluster containing [Mo2O2(mu-S)(2)(C6H5O7)(C6H4O7)](5-) anion was synthesized and characterized by elemental analysis, IR, UV-Vis spectra, XPS and X-ray diffraction. The parameters of the crystal structure of the compound are monoclinic, space group P2(1)/c, a = 2. 376 6(5) nm, b = 1. 327 4(3) nm, c = 2. 247 1(5) nm, beta = 118. 21 degrees, V = 6. 247(2) nm(3), Z = 8, D-c = 2. 128 g/cm(3), F(000) = 3 984, mu = 1 694 cm(-1), R = 0. 083 1 and R-2,R-w = 0. 154 9. The anion is binuclear molybdenum-citrato complex with mu(2)-S bridge. Each molybdenum atom pocesesses a distorted octahedral struture, which is coordinated with a terminal oxygen, two sulfur atoms, three oxygen atoms of hydroxyl, alpha-carboxylate, beta-carboxylate from citrate.