复边藓在中国的重新发现

Cinclidotus fontinaloides (Hedw ) P Beauv,which was previously collected and reported only once from Tibet in 1859 by Mitten,was rediscovered from Xinjiang (Mt Tianshan),China The description and illustrations of the species based on Chinese collection is presented in details for the first time in China

科尔沁草甸草地放牧和割草条件下土壤种子库研究

研究了科尔沁沙地草甸草地在放牧、割草两种利用方式下的土壤种子库的大小、组成及其与地上植被的关系 .结果表明 ,在自由放牧下 ,土壤种子库密度为 6 15 8± 16 4 7粒·m-2 ,在割草利用下 ,土壤种子库密度为 8312± 2 5 4 0粒·m-2 .放牧干扰下 ,种子库组成以矮小、短命的一年生植物为主 ,其中一二年生植物占 81 6 6 % ,占比例最大的前 4种植物分别为虎尾草 (38 5 5 % )、灰绿藜 (15 4 2 % )、毛马唐 (14 95 % )和狗尾草 (9 83% ) ,多年生植物种子密度仅为 112 9± 30 2粒·m-2 ;割草干扰下 ,一二年生植物占6 8 0 8% ,其中狗尾草占 5 2 7% ;而割草地多年生植物种子密度为 2 6 5 3± 811粒·m-2 放牧地土壤种子库密度与地上植物相关不显著 ;割草地土壤种子库密度与地上植物多度显著相关 (r=0 76 ,P <0 0 1) .放牧地种子库的Shannon Wiener指数、丰富度指数分别为 2 96和 2 98,明显小于割草地的 3 10和 5 0 9,表明自由放牧更易使物种多样性下降 .

外源添加物对秸秆还田土壤中无机氮转化影响

采用室内培养方法,研究秸秆不同还田方式土壤中加入无机氮肥和玉米秸秆对无机氮转化的影响。在田间秸秆不同还田处理的土壤中加入氮肥(硫酸铵)培养,初期土壤NH_4~+-N的含量较高,随着培养时间延长,NH_4~+-N的含量下降,培养15天后NH_4~+-N的含量趋于平衡;而土壤中NO_3~--N含量在培养期间逐渐增加,培养30天后NO_3~--N含量趋于平衡;秸秆不同还田处理土壤中添加秸秆培养,粉碎还田处理的土壤中NH_4~+-N的含量在整个培养过程中处于最低,培养后期覆盖还田和高茬还田的土壤NH_4~+-N的含量略有下降。

Multifunctional metallophosphors with anti-triplet–triplet annihilation properties for solution-processable electroluminescent devices

With the goal to provide organometallic triplet emitters with good hole-injection/hole-transporting properties, highly amorphous character for simple solution-processed organic light-emitting diodes, and negligible triplet-triplet (T-T) annihilation, a series of new phosphorescent cyclometalated Ir-III and Pt-II complexes with triphenylamine-anchored fluorenylpyridine dendritic ligands were synthesized and characterized. The photophysical, thermal, electrochemical and electroluminescent properties of these molecules are reported.

Solvent Vapor-Induced Self Assembly and its Influence on Optoelectronic Conversion of Poly(3-hexylthiophene): Methanofullerene Bulk Heterojunction Photovoltaic Cells

Nanoscale-phase separation of electron donor/acceptor blends is crucial for efficient charge generation and collection in Polymer bulk heterojunction photovoltaic cells. We investigated solvent vapor annealing effect of poly(3-hexylthiophene) (P3HT)/methanofullerene (PCBM) blend oil its morphology and optoelectronic properties. The organic solvents of choice for the treatment have a major effect oil the morphology of P3HT/PCBM blend and the device performance. Ultraviolet-visible absorption spectro,;copy shows that specific solvent vapor annealing can induce P3HT self-assembling to form well-ordered structure; and hence, file absorption in the red region and the hole transport are enhanced. The solvent that has a poor Solubility to PCBM Would cause large PCBM Clusters and result in a rough blend film. By combining an appropriate solvent vapor treatment and post-thermal annealing of the devices, the power conversion efficiency is enhanced.

White electroluminescence from a single polymer system: Improved performance by means of enhanced efficiency and red-shifted luminescence of the blue-light-emitting species

High-efficiency white electrolurninescence from a single polymer is achieved by enhancing the electroluminescence efficiency and effecting a red-shift in the emission spectrum of the blue emissive species. A single-layer device of the resultant polymer exhibits a higher luminous efficiency than the nonmodified species (12.8 cd A(-1), see figure) and an external quantum efficiency of 5.4 % with CIE coordinates of (0.31,0.36), exemplifying the success of the reported methodology.

Brittle-ductile transition in high-density polyethylene/glass-bead blends: Effects of interparticle distance and temperature

The toughness of high-density polyethylene (HDPE)/glass-bead blends containing various glass-bead contents as a function of temperature was studied. The toughness of the blends was determined from the notch Izod impact test. A sharp brittle-ductile transition was observed in impact strength-interparticle distance (ID) curves at various temperatures. The brittle-ductile transition of HDPE/glass-bead blends occurred either with reduced ID or with increased temperature. The results indicated that the brittle-ductile-transition temperature dropped markedly with increasing glass-bead content. Moreover, the correlation between the critical interparticle distance (ID.) and temperature was obtained. Similar to the ID, of polymer blends with elastomers, the ID, nonlinearly increased with increasing temperature. However, this was the first observation of the variation of the ID, with temperature for polymer blends with rigid particles. (C) 2001 John Wiley & Sons, Inc. J Polym. Sci Part B: Polym. Phys 39: 1855-1859, 2001.

Gas permeation properties of cardo polyaryletherketones containing different alkyl substituents

The gas permeation properties of a series of cardo polyaryletherketone materials are reported, In this series, the hydrogen atoms of benzene rings on the backbone are systematically replaced with different alkyl substituents. The effects of temperature and structure variation on gas permeability and selectivity are discussed in detail. The experimental results revealed that the polyetherketone obtained by the introduction of dimethyl and diisopropyl substituents to phenolphthalein unit is 3 similar to 6 times more permeable than the unmodified one for the gases studied.

Structure of hydrated dysprosium picolinate, [Dy(C5H4NCO2)(3)(H2O)(2)]2.8H(2)O

The crystal structure of the title compound was determined by X-ray diffraction. The dysprosium ion is eight-coordinated by three oxygen atoms and three nitrogen atoms from three picolinato ions and two water oxygen atoms. The nitrogen atom and one carboxyl oxygen atom of each picolinato ion are coordinated to the same dysprosium ion to form a five-membered chelating ring. The title compound exists as discrete molecules in the crystal structure.

含不同取代基的Cardo聚芳醚酮的气体透过性能

研究了带有不同烷基取代基的Ｃａｒｄｏ聚芳醚酮均质膜对Ｈ２、Ｏ２、Ｎ２、ＣＯ２和ＣＨ４气体的透气性能，讨论了气体透过对温度的依赖性。与未改性酚酞聚芳醚酮相比，在主链苯环上引入异丙基侧基会使气体透过系数提高３～６倍；每个结构单元苯环被４个甲基取代后，气体透过系数和选择分离系数同时得到较大改善，其中Ｈ２的透过系数为２２ｂａｒｒｅｒ，Ｈ２／Ｎ２分离系数为１１４。

ELECTROCHEMICAL STUDY OF ISOPOLY-OXOMETALLATE AND HETEROPOLY-OXOMETALLATE FILM MODIFIED MICROELECTRODES .2. ELECTROCHEMICAL-BEHAVIOR OF ISOPOLYMOLYBDIC ACID MONOLAYER MODIFIED CARBON-FIBER MICROELECTRODES

In this paper the electrochemical properties of isopolymolybdic anion thin film modified carbon fibre (CF) microelectrode prepared by simple dip coating have been described. The modified electrode shows three couples of surface redox waves between + 0.70 and - 0.1 V vs. sce in 2 M H2SO4 solution with good stability and reversibility. The pH of solution has a marked effect on the electrochemical behaviour and stability of the film, the stronger the acidity of electrolyte solution is, the better the stability and reversibility of isopolymolybdic anion film CF microelectrode will be. The scanning potential range strongly influences on the electrochemical behaviour of the film. The isopolymolybdic anion film prepared by the dip coating resulting a monolayer with estimated surface concentration (F) 2.8 x 10(-11) mol cm-2. From the half-peak widths and peak areas of the surface redox waves of the film electrode, the first three surface waves are corresponding to two-electron processes. The electron energy spectra show the products by six electrons reduction are a mixture of Mo(VI) and Mo(V) species. The electrochemical reaction of the isopolymolybdic anion monolayer can be expressed as Mo8O264- + mH+ + 2ne half arrow right over half arrow left [HmMo8-2n(VI)Mo2n(V)O26](4,2n-m)-n = 1, 2, 3; m = 2, 5, 7.

Seasonal and interannual variability of primary and export production in the South China Sea: a three-dimensional physical-biogeochemical model study

To investigate the seasonal and interannual variations in biological productivity in the South China Sea (SCS), a Pacific basin-wide physical - biogeochemical model has been developed and used to estimate the biological productivity and export flux in the SCS. The Pacific circulation model, based on the Regional Ocean Model Systems (ROMS), is forced with daily air-sea fluxes derived from the NCEP (National Centers for Environmental Prediction) reanalysis between 1990 and 2004. The biogeochemical processes are simulated with a carbon, Si(OH)(4), and nitrogen ecosystem (CoSiNE) model consisting of silicate, nitrate, ammonium, two phytoplankton groups (small phytoplankton and large phytoplankton), two zooplankton grazers (small micrograzers and large mesozooplankton), and two detritus pools. The ROMS-CoSiNE model favourably reproduces many of the observed features, such as ChI a, nutrients, and primary production (PP) in the SCS. The modelled depth-integrated PP over the euphotic zone (0-125 m) varies seasonally, with the highest value of 386 mg C m (-2) d (-1) during winter and the lowest value of 156 mg C m (-2) d (-1) during early summer. The annual mean value is 196 mg C m (-2) d (-1). The model-integrated annual mean new production (uptake of nitrate), in carbon units, is 64.4 mg C m (-2) d (-1) which yields an f-ratio of 0.33 for the entire SCS. The modelled export ratio (e-ratio: the ratio of export to PP) is 0.24 for the basin-wide SCS. The year-to-year variation of biological productivity in the SCS is weaker than the seasonal variation. The large phytoplankton group tends to dominate over the smaller phytoplankton group, and likely plays an important role in determining the interannual variability of primary and new production.

Bromophenols coupled with methyl gamma-ureidobutyrate and bromophenol sulfates from the red alga Rhodomela confervoides

Four new bromophenols C-N coupled with methyl gamma-ureidobutyrate (1-4), a phenylethanol bromophenol (5), and three phenylethanol sulfate bromophenols (6-8) have been isolated from polar fractions of an ethanolic extract of the red alga Rhodomela confervoides. On the basis of spectroscopic evidence including HRMS and 2D NMR data, the structures of the new compounds were determined as methyl N'-(2,3-dibromo-4,5-dihydroxybenzyl)-gamma-ureidobutyrate (1), methyl N,N'-bis(2,3-dibromo-4,5-dihydroxybenzyl)-gamma-ureidobutyrate (2), methyl N'-[3-bromo-2-(2,3-dibromo-4,5-dihydroxybenzyl)-4,5-dihydroxybenzyl]-gamma-ureidobutyrate (3), methyl N'-(2,3-dibromo-4,5-dihydroxybenzyl)-A7-[3-bromo2-(2,3-dibromo-4,5-dihydroxybenzyl)-4,5-dihydroxybenzyl]-gamma-ureidobutyrate (4), 2,3-dibromo-4,5-dihydroxyphenylethanol (5), 2,3-dibromo-4,5-dihydroxyphenylethanol Sulfate (6), 3-bromo-4,5-dihydroxyphenylethanol sulfate (7), and 3-bromo2-(2,3-dibromo-4,5-dihydroxybenzyl)-4,5-dihydroxyphenylethanol sulfate (8). The cytotoxicity of all compounds was evaluated against several human cancer cell lines including human colon cancer (HCT-8), hepatoma (Bel7402), stomach cancer (BGC-823), lung adenocarcinoma (A549), and human ovarian cancer (A2780). Among them, the phenylethanol and the phenylethanol sulfate bromophenols (5-8) showed moderate cytotoxicity against all tested cell lines.