林带疏透度数字化测度方法的改进及其应用研究

在大量野外调查基础上 ,用数码相机拍摄林带相片 ,采用CIAS软件测定林带疏透度 ,对已有“数字图像处理法”进行了改进 ,并对疏透度的变化规律进行了深入研究 .结果表明 ,用改进的数字化方法测定林带的疏透度 ,比用光学相机所进行的“数字图像处理法”精度高 ,更经济、简捷 ;林带疏透度 β与相对枝下高x(枝下高 /林带平均高 )的关系无叶期可表达为 β =1.0 6 81x0 .4 3 0 4 (r =0 .976 3,r0 .0 1=0 .40 73) ;有叶期可表达为 β =0 .6 72x0 .4 69(r =0 .985 1,r0 .0 1=0 .40 73) (0≤β≤ 1) ;β随着林龄a呈抛物线式变化 ,β =0 0 0 0 9a2 - 0 .0 36 4a +0 .6 82 8(0≤β≤ 1) ;提出的林带断面疏透度 β0 是定量反映林带断面结构的定量评价指标 ,同时可作为评价林带结构的辅助指标 ;提出混交林带的疏透度计算式 β =(β1n1+β2 n2 ) / (n1+n2 ) ;在相同配置不同树种的纯杨、柳、榆林带结构以杨树林带结构较好 ,柳树林带结构次之 ,疏透度值 βPPP<βSSS<βUUU;在树种相同、配置不同时 ,品字形优于矩形 ;杨柳榆的混交林带中杨榆株间、杨柳对称式行间SPPS混交方式结构防护效果较好

水土保持科研与管理专家王万忠研究员

王万忠研究员 ,男 ,生于 1 95 2年 ,陕西省临潼县人。 1 976年毕业于陕西师范大学地理系 ,分配到中国科学院水利部水土保持研究所工作至今。 1 988年担任科研处处长 ,1 991年任中国科学院黄土项目办公室副主任 ,1 994年 9月 ,以高级访问学者身份赴日本东京大学、宫崎大学访问 ,1 995年任副所长 ,现任西北农林科技大学党委副书记 ,硕士研究生导师。王万忠研究员 ,长期从事土壤侵蚀与水土保持研究工作 ,曾主持国家“八五”攻关专题“黄土高原区域水土保持与农业发展综合研究”,国家“九五”攻关子专题“水土保持效益区域性评估及主体措施配置”,中国科学院知识创新项目子专题“高强度治理下黄土高原水土流失预测”以及“中国降雨侵蚀力研究”等项目。其中国家“八五”攻关专题“黄土高原区域水土保持与农业发展综合研究”获 1 998年中国科学院科技进步二等奖 ,他本人也被国家计委、国家科委及财政部授予“八五”国家科技攻关先进个人 ,受到江泽民总书记的接见。出版专著 2部 ,参编专著 2部 ,发表论文 2 0余篇 ,其中专著《黄土高原降雨侵蚀产沙与黄河输沙》、《黄土高原降雨侵蚀产沙数据图集》,以及论文“黄土地区...

Free-Radical Solution Copolymerization of the Ionic Liquid Monomer 1-Vinyl-3-Ethylimidazolium Bromide with Acrylonitrile

Ionic liquid monomer 1-vinyl-3-ethylimidazolium bromide (ViEtIM(+)Br(-)) was first used to copolymerize with acrylonitrile (AN) successfully under various conditions. This was achieved with azobisisobutyronitrile as the initiator and dimethyl sulfoxide as the solvent. The kinetics of this copolymerization were studied. The values of the monomer apparent reactivity ratios were calculated by the Kelen-Tudos method. The apparent reactivity ratios of ViEtIM(+)Br(-) (r(ViEtIM+Br-)) and AN (r(AN)) were similar at polymerization conversions of less than 10%, (r(AN) = 0.954, r(ViEtIM+Br-) = 0.976). The copolymers were obtained with high molecular weights and high hydrophilicides. The copolymers were characterized by H-1-NMR, differential scanning calorimetry, and thermogravimetric analysis. These copolymers may be potentially useful in the preparation of precursor fibers and carbon fibers.

CoTPP-Pt/C作直接甲醇燃料电池阴极催化剂

制备了炭载四苯基钴卟啉(CoTPP)和Pt(CoTPP-Pt/C)复合催化剂,研究了炭载四苯基铁卟啉对氧还原的电催活性。电化学研究发现,CoTPP-Pt/C催化剂对氧还原有很高的电催化活性。CoTPP-Pt/C催化剂对氧还原的极限电流密度比Pt/C催化剂高30%左右,但抗甲醇的能力未改善。

Self-assembly of crystalline-coil diblock copolymer in solvents with varying selectivity: From spinodal-like aggregates to spheres, cylinders, and lamellae

We have investigated systematically the morphology of thin films spin-coated from solutions of a semicrystalline diblock copolymer, poly(L-lactic acid)-block-polystyrene (PLLA-b-PS), in solvents with varying selectivity. In neutral solvents (chloroform and tetrahydrofuran (THF)), a spinodal-like pattern was obtained and the pattern boundary was sharpened by diluting the solution. Meanwhile, loose spherical associates, together with larger aggregates composed of these associates by unimer bridges, formed partly due to crystallization of the PLLA blocks in relatively concentrated solutions. In slightly PS-selective solvent (e.g., benzene), both loose and compact spherical micelles were obtained, depending on the polymer concentration, coexisting with unimers. When enhancing the selectivity with mixed solvents, for example, mixing the neutral solvent and the slightly selective solvent with a highly PS-selective solvent, CS2, loose assemblies (nanorods in CS2/THF mixtures and polydisperse aggregates in CS2/benzene mixtures) and well-developed lamellar micelles were obtained.

Synthesis and crystal structure of bis(tetrahydrofurfurylindenyl) lanthanide chlorides

Lanthanocene chlorides (C4H7OCH2C9H6)(2)LnCl[Ln=Y(1); Ln=Gd(2)] were synthesized by the reaction of tetrahydrofurfurylindenyl lithium(in situ) with corresponding anhydrous lanthanide chorides in THF. The crystal structures of these two complexes were determined by X-ray diffraction and they were unsolvated monomeric complexes. They were stable in the air for several hours. Complexes 1 and 2 belong to the same crystal system (orthorhombic) and space group(P2(1)2(1)2(1)). The unit cell dimensions of complex 1 were a=1.042 52(9) nm, b=1.47455(12) nm, c=1.497 99(13) nm, Z=4, D-c=1.508 g/cm(3); The unit cell dimensions of complex 2 were a=1.037 01(10) nm, b=1.472 33(12) nm, c=1.513 54(14) nm, Z=4, D-c=1.699 g/cm(3). They have the same structure and different space configurations. The central metal atom is coordinated by two indenyl, two oxygen of the tetrahydrofurfuryl and one chlorine atom to form a distorted trigonal bipyramid.

Capillary liquid chromatographic-high-resolution mass spectrometric analysis of ribonucleotides

A method of capillary HPLC-high-resolution MS was developed for the trace analysis of ATP, GTP, dATP and dGTP Dimethylhexylamine (DMHA) was used as ion-pairing agent for the HPLC retention and separation of the nucleotides and positive ion electrospray time-of-flight MS was used for the detection. The application of capillary HPLC allowed minimal usage of DMHA while providing excellent peak retention and resolution, which significantly reduced the ion suppression in electrospray ionization-MS analysis and thus increased the sensitivity. Adduct ions of nucleotides and DMHA were used as quantitative ions in order to achieve the best sensitivity. DMHA concentration at 5 mM in the aqueous mobile phase at pH 7 was found to be the optimal conditions for the C Is capillary column. The method was applied to determine ATP level in cultured C6 glioma cells that were treated with toxic concentrations of Zn. The results showed that the cellular ATP level decreased from 2.7 pmol/cell (<10% cell death) in average control cell samples to 0.36 pmol/cell as the concentration of Zn increased to 120 mg/l (>35% cell death) in culture medium.

Epitaxial crystallization of sPP on the (100) lattice plane of HDPE crystals

Crystallization behavior of syndiotactic polypropylene(sPP) on the (100) lattice plane of high-density polyethylene(HDPE) crystals was studied by means of transmission electron microscopy and electron diffraction. The results indicate that sPP crystals can grow epitaxially on the (100) PE lattice plane with their chain directions +/-37 degrees apart from the chain direction of the HDPE substrate. The contact planes are (100) lattice planes for both polymers. This kind of epitaxy is explained in terms of parallel alignment of HDPE chains along the rows formed by the {CH3, CH2,CH3} groups in the (100) lattice plane of the sPP crystals. This implies that in the epitaxial crystallization of sPP with fiber oriented HDPE substrate, not only the (110) but also the (100) HDPE lattice planes can act as the oriented nucleation sites. Furthermore, according to the poor matching between HDPE chains in the (100) lattice plane and the {CH3, CH2, CH3} group rows in the (100) lattice plane of the sPP crystals, it is concluded that the geometric matching is not the only controlling factor for the occurrence of polymer epitaxy.

间同立构聚丙烯在聚乙烯(100)晶面上的附生行为研究

利用电子显微镜的欠焦成像和电子衍射技术对间同立构聚丙烯（ｓＰＰ）在高密度聚乙烯（ＨＤＰＥ）的（１００）晶面上的结晶行为进行了研究．明场结果表明，ｓＰＰ能在ＨＤＰＥ的（１００）晶面上附生生长，形成相互交叉的草席状片晶结构．电子衍射结果证明，附生生长的ｓＰＰ与ＨＤＰＥ的接触面为（１００）晶面，ｓＰＰ与ＨＤＰＥ的分子链方向成固定的±３７°交角．说明ｓＰＰ在纤维取向的ＨＤＰＥ基质上附生结晶不仅仅是ＨＤＰＥ的（１１０）晶面对ｓＰＰ有取向成核作用，（１００）ＨＤＰＥ晶面也可作为ｓＰＰ晶体的取向成核点

STUDIES ON OLEFIN-COORDINATING TRANSITION-METAL CARBENE COMPLEXES .20. SYNTHESIS OF 1,3-CYCLOHEXADIENE(DICARBONYL) [ETHOXY(ARYL)-CARBENE]IRON COMPLEXES AND THEIR PHOSPHINE ADDUCTS - CRYSTAL-STRUCTURE OF C6H8(CO)2FEC(OC2H5)C6H4CH3-O

Reaction of 1,3-cyclohexadiene(tricarbonyl)iron (1) with ortho-substituted aryllithium reagents ArLi (Ar=o-CH3C6H4, o-CH3OC6H4, o-CF3C6H4) in ether at low temperature, and subsequent alkylation of the acylmetalates formed with Et3OBF4 in aqueous solution at 0-degrees-C or in CH2Cl2 at -60-degrees-C gave the 1,3-cyclohexadiene(dicarbonyl)[ethoxy(aryl)carbene]iron complexes (eta4-C6H8)(CO)2FeC(OC2H5)Ar (3, Ar = o-CH3C6H4; 4, Ar = o-CH3OC6H4), and the isomerized product (eta3-C6H8)(CO)2FeC(OC2H5)C6H4CF3-o (5), respectively, among which the structure of 3 has been established by an X-ray diffraction study. Complex 3 is monoclinic, space group P2(1) with a = 8.118(4), b = 7.367(4), c = 14.002(6) angstrom, beta = 104.09(3)-degrees, V = 812.2(6) angstrom3, Z = 2, D(c) = 1.39 g cm-3, R = 0.056, and R(w) = 0.062 for 976 observed reflections. Complexes 3 and 5 were converted into the chelated allyliron phosphine adducts(eta3-C6H8)(CO)2(PR31)FeC(OC2H5)Ar (6, Ar = o-CH3C6H4, R1 = Ph; 7, Ar = o-CH3C6H4, R1 = OPh; 9, Ar = o-CF3C6H4, R1 = Ph), by reaction with phosphines in petroleum ether at low temperatures.

多功能高灵敏度双恒电位仪的研制及应用

研制了一种可测量pA～mA级电流的高灵敏度多功能双恒电位仪。此仪器结构简单,灵活性强,操作方便。成功地应用于微电极电化学检测器的液相色谱/电化学研究。

STUDY ON THE FORMATIONAL MECHANISM OF THE NORTHERN YELLOW (HUANGHAI) SEA COLD WATER MASS(I)

A hydrodynamic-thermodynamic equation set was set up to reflect the formational mechanism and evolution of the Northern Yellow (Huanghai) Sea cold water mass (NYSCWM) and its density circulation. Appropriate mathematical physical models were established by using some physical postulations. An approximate analytic solution to expound the distributions of temperature and three-dimensional current velocity, which can be used to expound the formational mechanism of the NYSCWM and its density circulation is obtained by using the theory of boundary layer and perturbational analyses.

海水鱼细胞系FG、SPH和RSBF的特性分析及其在典型海洋污染物毒性检测上的应用

鱼类细胞培养已成为鱼类病毒学、肿瘤学、毒理学、遗传学和免疫学等研究的重要手段。本文首先从形态、蛋白质（同工酶）和DNA（RAPD分析）三个层次水平对牙鲆鳃细胞系FG、鲈鱼心脏细胞系SPH和真鲷鳍细胞系RSBF的特性进行了分析，并分别与其所对应的原代培养组织作了比较。形态、蛋白质和DNA分析的结果表明：(1) 三株海水鱼细胞系的乳酸脱氢酶(LDH)酶谱彼此明显不同，可作为对它们进行种属鉴定和交叉污染鉴别的有效遗传标记；(2)与所对应的原代培养组织的LDH酶谱相比，细胞系FG的LDH酶谱维持不变，而细胞系SPH和FRSBF的LFH酶酶谱变化较大；(3)与所对应的原代培养细胞的形态相比，细胞系FG的细胞形态没有明显改变，而细胞系SPH和RSBF的细胞形态则发生了明显改变；(4)60个DNA随机引物对三株细胞系及其原代培养组织的RAPD分析表明，有35－48％的引物在细胞系及其原代培养组织之间产生完全相同的RAPD指纹，为这三株细胞系种属来源的鉴别奠定了基础，另有27－32％的引物在细胞系及其原代培养组织之间产生不同的RAPD指纹，表明这三株细胞系中发生了遗传变异；(5)FG、SPH和RSBF三株细胞系与其所来源鱼类个体间的总遗传相似性指数大小为0.825-0.851，这表明了它们之间的同源性，同时为我们采用RAPD技术对其它细胞系进行种属鉴定提供了可供参考的实验数据；(6)筛选得到四个随机引物S－91、S－223、S－228和S－237，分别可参在这三株海水鱼细胞系中扩增得到特异性的彼此明显不同的RAPD指纹，这些特异性RAPD指纹在各细胞系与其原代培养组织之间，以及在细胞系的传代培养过程中是稳定的，因而这四个引物对于这三株细胞系的种属鉴定、交叉污染检测以及监测它们与其来源鱼类个体之间的遗传变异将非常有用。其次，170代以后的FG细胞发生了自发性肿瘤转化，具有了在细胞单层上聚集生长和堆积生长的能力，本文对转化前后细胞的形态、贴壁依赖性(软琼脂克隆形成实验)和遗传物质稳定性(RAPD分析)进行分析的结果表明：FG细胞失去接触抑制和生长的密主抑制，获得在细胞单层上聚集生长和堆积生长能力的同时，也获得了在软琼脂中生的能力(8－14个克隆/10~6个接种细胞)；RAPD分析表明，转化前后FG细胞的RAPD指纹发生了明显的变异。因此，FG细胞的自发性肿瘤转化也如哺乳动物细胞一样，包括一系列不断进行的细胞学和遗传学变化，并最终导致其基因组DNA的遗传变异。最后，本文分析了聚乙烯亚胺(PEI)和氯化镍在RSBF细胞中的细胞毒性和基因毒性，结果表明：鱼类细胞系RSBF可作为一个有效的检测水环境中污染的细胞毒性和基因性效应的效应的筛选系统；RAPD分析可作为一个灵敏的非专一性的基因毒性检测终点；PEI对RSBF细胞的高细胞毒性和基因毒性表明，我们在利用PEI作基因载体进行人类基因冶疗和进行鱼类转基因实验时要格外慎重；镍及其化合物可能是导致鱼类肿瘤性疾病的原因之一。

Characterization of 12 single nucleotide polymorphisms (SNPs) in Pacific abalone, Haliotis discus hannai

We report here for the first time 12 polymorphic single nucleotide polymorphisms (SNPs) in a commercially important gastropod, Pacific abalone (Haliotis discus hannai) that were identified by searching expressed sequence tag database. These SNP loci (seven nuclear and five mitochondrial SNPs) were polymorphic among 37 wild abalone individuals, based on a four-primer allele-specific polymerase chain reaction analysis. All loci had two alleles and the minor allele frequency ranged from 0.027 to 0.473. For the seven nuclear SNPs, the expected and observed heterozygosities ranged from 0.053 to 0.499 and from 0.054 to 0.811, respectively.