长白山阔叶红松林昆虫多样性研究

通过季节性观察 ,系统地研究了长白山阔叶红松林昆虫类群及其多样性 .结果表明 ,长白山阔叶红松林已知的森林昆虫 2 6目 131科 116 2属 196 0种 ,其中森林害虫 11目 10 5科 881种、重要森林害虫6 38种 ;森林昆虫群落中植食性昆虫类群总数所占比重最大 ,天敌昆虫群落中以捕食性类群总数所占比重最大 .植食类群、寄生性类群和捕食类群全年的均匀度指数分别为 0 884、0 830和 0 80 6 .各类群间季节变动系数的大小顺序为捕食类群 >寄生性类群 >植食类群 .

黄土高原水土流失区人口、粮食发展模式与有关政策探讨

本文以西部大开发战略为指导，采用整体、系统、宏观、多维的思路，由综合研究到单项研究再到分区研究，由理论到实例，由定性到定量，由质量到数量，对黄土高原水土流失区做了系统全面的研究，以1949～1995年资料为基础，剖析了黄土高原水土流失区人口、粮食发展模式在发展过程中存在的难点和焦点问题，针对该区的自然条件与农业生产中的优势与问题，提出了技术体系，讨论了有关政策问题。

美国的土壤侵蚀与防治

<正> 美国是世界农业大国,除遇特大自然灾害外,农业生产一直保持长期稳定发展的态势.1990年谷物的生产量达到3.13亿t,预测到2000年谷物产量可达4.53亿t,1985～2000年谷物平均增长速度为1.8%.美国的农业生产之所以能取得如此辉煌的成就有多种原因,其中政府重视土壤保护是最主要的原因之一.80年代初期,美国的农业科学家皮门特尔就曾向全世界发出警告,指出土壤侵蚀已成为全世界第一号环境问题,呼吁人们注意土壤侵蚀给农业生产带来的严重危害.而当时的美国同样面临着土壤侵蚀的严峻形势.深入的研究表明,土壤侵蚀恶性发展的根本原因不在气候变异、水旱等自然灾害,造成土壤侵蚀的根本原因来自人类对自然界的干扰,其中包括不合理的土地利用、滥砍滥伐、破坏森

大气沉降核素~(7)Be在黄土高原地被物中的分布初探

7Be具有环境微粒示踪价值,在示踪土壤侵蚀研究中有一定的应用,但是有关地被覆盖物对7Be截留吸收的研究目前还相当少,这直接影响了示踪结果的准确性、示踪模型的建立及应用。本文对不同地被物中的7Be含量进行了分析,结果表明:春季末地表不同地被覆盖物中干枯植物的7Be含量最大,半分解物次之,活植物中含量最少。在整个植物生长期内,植物体7Be累积含量呈增长趋势,尤其在秋季增加更为突出;不同植物中7Be含量差异性很大,变异系数达0.6;从总体上看,不同类型植物中7Be的平均含量分布趋势是草本>半灌木及小灌木>种植作物;和其它同类植物种相比,不同作物种中7Be含量的变异系数相对较大,为0.47。

沙地云杉新种的鉴定及其对我国北方生态环境建设意义

在浩瀚无垠的小腾格里沙地东部边缘，生态环境非常脆弱地区、分布着大面积的原始云杉天然林，是世界上非常罕见特殊的森林生态系统类型．但是长期以来，这种云杉究竞是哪一种？在我国植物分类学上一直是个争论性问题．我国著名树木分类学家郑万钧教授在《中国植物志》第七...

远紫外辐射对紫杉幼苗针叶膜脂过氧化及内源保护系统的影响

实验室条件下用远紫外线 (UV BC)光源照射紫杉幼苗 ,随照射时间延长 ,针叶的离子渗出率、膜脂过氧化水平、组织自动氧化速率及H2 O2 含量显著增加 ,可溶性蛋白、抗坏血酸、类胡萝卜素和叶绿素含量下降 ,叶绿体光系统II电子传递活性显著下降 ,外源活性氧清除剂苯甲酸钠和抗坏血酸对针叶膜脂过氧化有抑制作用 ;甲基紫精和DDC对针叶膜脂过氧化有促进效果 ,远紫外线引起的紫杉伤害可能和针叶树的越冬光氧化伤害有类似之处 .紫杉苗对紫外辐射的抗性远高于一般农作物 .

内蒙古呼伦贝尔市饮茶型氟铝联合中毒研究

目的探讨饮茶型氟中毒是否为砖茶型氟铝联合中毒。方法对饮茶型氟中毒病区进行饮水、砖茶、奶茶、主食、副食及牧民发、血、尿氟铝水平检测,对饮茶型氟中毒病区儿童和成人进行临床检查和拍摄X线片,同时对成人进行血液生物化学检查,以饮水型病区及非病区居民为对照组。结果呼伦贝尔市饮茶型病区饮水、主食、副食氟铝水平均在正常范围,砖茶氟铝水平分别为(541.3±48.8)、(4351±724)mg/kg,奶茶氟铝水平分别为(3.83±0.73)、(4.28±1.56)mg/L。饮水型病区饮水氟铝水平分别为(3.68±1.05)、(0.45±0.25)mg/L。饮茶型病区牧民氟总摄入量96.15%、铝总摄入量89.60%来源于砖茶。儿童氟斑牙检出率饮茶型病区为25.24%,饮水型病区为63.17%,饮茶型病区非常显著低于饮水型病区(P<0.01);成人氟中毒检出率饮茶型病区为42.61%,饮水型病区为28.83%,饮茶型病区显著高于饮水型病区(P<0.01)。结论呼伦贝尔市饮茶型氟中毒发病机理较为复杂,可能是砖茶型氟铝联合中毒。

The rheological behavior and dynamic mechanical properties of syndiotactic 1,2-polybutadiene

The rheological behavior and the dynamic mechanical properties of syndiotactic 1,2-polybutadiene (sPB) were investigated by a rotational rheometer (MCR-300) and a dynamic mechanical analyzer (DMA-242C). Rheological behavior of sPB-830, a sPB with crystalline degree of 20.1% and syndiotactic content of 65.1%, showed that storage modulus (G ') and loss modulus (G '') decreased, and the zero shear viscosity (eta(0)) decreased slightly with increasing temperature when measuring temperatures were lower than 160 degrees C. However, G ' and G '' increased at the end region of relaxation curves with increasing temperature and)10 increased with increasing temperature as the measuring temperatures were higher than 160 degrees C. Furthermore, critical crosslinked reaction temperature was detected at about 160 degrees C for sPB-830. The crosslinked reaction was not detected when test temperature was lower than 150 degrees C for measuring the dynamic mechanical properties of sample. The relationship between processing temperature and crosslinked reaction was proposed for the sPB-830 sample.

Polypropylene as a carbon source for the synthesis of multi-walled carbon nanotubes via catalytic combustion

Multi-walled carbon nanotubes (MWCNTs) were efficiently synthesized by catalytic combustion of polypropylene (PP) using nickel compounds (such as Ni2O3, NiO, Ni(OH)(2) and NiCO3 (.) 2Ni(OH)(2)) as catalysts in the presence of organic-modified montmorillonite (OMMT) at 630-830 degrees C. Morphologies of the sample undergoing different combustion times were observed to investigate actual process producing MWCNTs by this method. The obtained MWCNTs were characterized by X-ray diffraction (XRD), transmission electron microscope and Raman spectroscopy. The yield of MWCNTs was affected by the composition of PP mixtures with OMMT and nickel compounds and the combustion temperature. The proton acidic sites from the degraded OMMT layers due to the Hoffman reaction of the modifiers at high temperature played an important role in the catalytic degradation of PP to supply carbon sources that are easy to be catalyzed by nickel catalyst for the growth of MWCNTs. The XRD measurements demonstrated that the nickel compounds were in situ reduced into the Ni(0) state with the aid of hydrogen gas and/or hydrocarbons in the degradation products of PP, and the Ni(O) was really the active site for the growth of MWCNTs. The combination of nickel compounds with OMMT was a key factor to efficiently synthesize MWCNTs via catalytic combustion of PP.

Heterojunction ambipolar organic transistors fabricated by a two-step vacuum-deposition process

Ambipolar organic field-effect transistors (OFETs) are produced, based on organic heterojunctions fabricated by a two-step vacuum-deposition process. Copper phthalocyanine (CuPc) deposited at a high temperature (250 degrees C) acts as the first (p-type component) layer, and hexadecafluorophthalocyaninatocopper (F16CuPc) deposited at room temperature (25 degrees C) acts as the second (n-type component) layer. A heterojunction with an interpenetrating network is obtained as the active layer for the OFETs. These heterojunction devices display significant ambipolar charge transport with symmetric electron and hole mobilities of the order of 10(-4) cm(2) V-1 s(-1) in air. Conductive channels are at the interface between the F16CuPc and CuPc domains in the interpenetrating networks. Electrons are transported in the F16CuPc regions, and holes in the CuPc regions. The molecular arrangement in the heterojunction is well ordered, resulting in a balance of the two carrier densities responsible for the ambipolar electrical characteristics. The thin-film morphology of the organic heterojunction with its interpenetrating network structure can be controlled well by the vacuum-deposition process.

Polydispersity of ethylene sequence length in metallocene ethylene/alpha-olefin copolymers. II. Influence on crystallization and melting behavior

In this work, crystallization and melting behavior of metallocene ethylene/alpha-olefin copolymers were investigated by differential scanning calorimetry (DSC) and atomic force microscopy (AFM). The results indicated that the crystallization and melting temperatures for all the samples were directly related to the long ethylene sequences instead of the average sequence length (ASL), whereas the crystallization enthalpy and crystallinity were directly related to ASL, that is, both parameters decreased with a decreasing ASL. Multiple melting peaks were analyzed by thermal analysis. Three phenomena contributed to the multiple melting behaviors after isothermal crystallization, that is, the melting of crystals formed during quenching, the melting-recrystallization process, and the coexistence of different crystal morphologies. Two types of crystal morphologies could coexist in samples having a high comonomer content after isothermal crystallization. They were the chain-folded lamellae formed by long ethylene sequences and the bundlelike crystals formed by short ethylene sequences. The coexistence phenomenon was further proved by the AFM morphological observation.

Isothermal and nonisothermal melt-crystallization kinetics of syndiotactic polystyrene

Analyses of the isothermal and nonisothermal melt kinetics for syndiotactic polystyrene have been performed with differential scanning calorimetry, and several kinetic analyses have been used to describe the crystallization process. The regime II-->III transition, at a crystallization temperature of 239degrees, is found. The values of the nucleation parameter K-g for regimes II and III are estimated. The lateral-surface free energy, sigma = 3.24 erg cm(-2), the fold-surface free energy, sigma(e) = 52.3 +/- 4.2 erg cm(-2), and the average work of chain folding, q = 4.49 +/- 0.38 kcal/mol, are determined with the (040) plane assumed to be the growth plane. The observed crystallization characteristics of syndiotactic polystyrene are compared with those of isotactic polystyrene. The activation energies of isothermal and nonisothermal melt crystallization are determined to be DeltaE = -830.7 kJ/mol and DeltaE = -315.9 kJ/mol, respectively.

Synthesis, structure characterization of the complexes of beta-alkoxycarbonylethyltin trichlorides with Schiff base ligands

Thirty - two title complexes (ROCOCHRCH2SnCl3)-C-1 . (2 - HOC6H4CH = NC6H4 - X) (R = Me, Et, n - Bu; R-1 = H, Me; X = H,4' - Cl, 3' - Pr, 3' - OH, 3', 4' - Cl-2, 4' - OMe) were synthesized and characterized by elemental analysis,UV - vis, IR, H-1 NMR. The crystal structure of n - BuOCOCH2CH2SnCl3 . (2 - HOC6H4CH - NC6H4OMe - 4') were determined by the X - ray diffraction analysis, The crystal belongs to monoclinic system, with a = 1.4661 (3)nm, b = 0.9307 (2)nm, c = 1.7888 (4)nm, beta = 94.04 (3)degrees, V = 2.4348nm(3), D-c = 1.581mg/m(3), Z = 4, F(000) = 1160, mu = 1.405mm(-1), R = 0.0354, R-w = 0,0486, space group: P2(1)/c. The complexes exist as a discrete monomer. The tin atom has a distorted octahedral geometry due to intramolecular coordination of the carbonyl oxygen and the phenolic oxygen of the Schiff base ligands, The coordination number of tin atom is 6.

β-烷氧羰乙基三氯化锡与Schiff碱配合物的合成、表征与结构

合成表征了32个标题化合物ROCOCHR~1CH_2SnCl_3·(2-HOC_6H_4CH=NC_6H_4-X)(R=Me,Et,n-Bu;R~1=H,Me;X=H,4’-Cl,3’-Br,3’-OH,3’,4’-Cl_2,4’-OMe),通过元素分析,UV-vis,IR和~1H NMR进行了表征n-BuOCOCH_2CH_2SnCl_3·(2-HOC_6H_4CH=NC_6H_4OMe-4’)的晶体结构分析表明,该晶体属单斜晶系,a=1.4661(3)nm,b=0.9307(2)nm,c=1.7888(4)nm,β=94.04(3)°;v=2.4348nm~3,Z=4;空间群P2_1/c.该化合物为含有分子内碳基氧配位,Schiff碱以酚羟基上的氧原子配位,中心锡原子为六配位,空间构型为畸变八面体构型的单分子有机锡化合物.