潮棕壤不同利用方式有机碳剖面分布及碳储量

对潮棕壤水稻田、玉米地、撂荒地和人工林地 4 种土地利用方式经过 14 年后在 0～150 cm 土体 10个土层中土壤有机碳含量的剖面分布、C/N 及有机碳储量进行比较研究。结果表明,不同利用方式下土壤有机碳含量产生明显的剖面分布差异。林地各土层有机碳含量较其它几种利用方式高,表明不同利用方式对土壤碳产生较大影响;土壤有机碳与全氮极显著相关,但自然生态系统中碳与氮的相关性略高于农田生态系统(林地R =0.990,撂荒地 R =0.990,稻田 R =0.976,玉米地 R =0.980,P < 0.001,n =30);剖面中 C/N 随深度而 2 2 2 2下降,林地 C/N 较高,稻田 C/N 较低,玉米地与撂荒地相应土层中 C/N 相近;在 100 cm 深度内,林地土壤分别比稻田、玉米地、撂荒地每年多截获 4.25、2.87 和 4.48 t·ha-1有机碳,年增幅分别为 6.15%、3.26%和 5.09%;林地有机碳储量显著高于稻田、玉米地和撂荒地(P 值分别达到 0.001、0.008 和 0.008),其它 3 种利用方式间差异不显著。据此认为林地在增加碳储量及改善环境方面具有很大的潜力。

菲对土壤酶活性的影响

采用室内培养方法,选择菲作为PAHs代表物,探讨了菲与土壤酶活性之间的关系。结果表明,当菲的添加浓度>100μg·kg-1时,添加菲后的3d时间里,土壤中脲酶活性有被抑制的现象;添加菲后的7d时间里,土壤中脱氢酶活性被抑制,土壤磷酸酶的活性却被激活;当菲的添加浓度为100～2400μg·kg-1时,土壤过氧化氢酶活性没有显著变化。土壤脲酶、脱氢酶、磷酸酶的活性可以作为菲污染土壤的生态毒理指标,并且观察它们在添加菲后的第1d到第7d的变化最为重要。

科尔沁沙地植被恢复及其对土壤的改良效应

探讨了对科尔沁沙地乌兰敖都地区流动沙丘采取生物和工程措施建立起人工固沙植被的相关配套技术,并就植被恢复程度对土壤改良效应进行了对比研究。结果表明:在流动沙丘进行人工固沙时采用1.0m×1.0m草方格内播种小叶锦鸡儿(Caraganamicrophylla)种子的措施具有较好的固沙效果,一般经过2年可使沙丘表面得到固定。在围栏封育条件下实施适宜的植被恢复措施,一般可在2~3年获得明显的固沙效果。小叶锦鸡儿人工固沙群落内土壤养分随着群落的生长发育而发生变化,在0~30cm土层中,有机质、速效钾、全氮、水解性氮、全磷、有效磷含量都表现为:11年生群落>6年生群落>流动沙丘;小叶锦鸡儿人工群落的建立可大幅度提高土壤微生物生物量,并随着年龄的增加,微生物生物量C、N、P的含量均呈现增加趋势。

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.