58 resultados para Haller, Johannes, 1487-1531.


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<正>1城市森林的概念及研究内容 1.1城市森林的提出及概念 城市森林这一概念的提出已有 30余历史,1962年,美国肯尼迪政 府在户外娱乐资源调查报告中,首 次使用“城市森林”这一名词。自 1965年加拿大Erik Jorgensen教授提 出城市林业概念以来,城市林业与 城市森林先后在北美、欧洲乃至全 球掀起了研究热潮。

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土地分类是土地评价、规划和管理的基础 ,对林业资源可持续利用具有重要的意义 .生态土地分类是目前土地分类的主要方向和趋势 ,国际上早已开展此项研究 .随着景观生态学和 3S技术的发展 ,生态分类系统的研制已成为生态土地分类的重点 .本文对生态土地分类的定义、特点、发展历史、生态分类系统理论 ,以及国际生态分类系统的发展趋势进行了系统的综述 ,并指出以资源 (森林、土地、水域等 )多目标管理为基础 ,定量与定性相结合的多因子多层次综合是未来生态土地研究发展的总趋势 ,有必要在我国大力开展相关研究 .

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介绍了土壤重金属的形态及各种分析方法,重点说明了土壤中重金属形态分布及影响因素;讨论了影响土壤环境中重金属形态转化的因素,重金属形态与重金属在土壤中的迁移性、可给性、活性的关系,重金属污染土壤修复与重金属形态分布的关系。形态分析在一定程度上反映自然与人为作用对土壤中重金属来源的贡献,并反映重金属的生物毒性。重金属可以因形态中某一个或几个方面不同而表现出不同的毒性和环境行为。

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应用生态学是迅猛发展的现代生态学的主体 .寻求解决人口、资源、环境等问题是应用生态学发展的主要动力 .经过 4 0年的发展 ,应用生态学已发展成为一个庞大的学科门类 .应用生态学未来的发展应更多地关注受人类影响和管理的生态系统并将人视为生态系统的组成成分 .应用生态学在当前和今后应给予优先重视的研究领域 ,包括生态系统与生物圈的可持续利用、生态系统服务与生态设计、转基因生物的生态学评价、生物入侵生态学、流行病生态学、生态预报、生态过程及其调控等 .在今后若干年内 ,围绕这些领域 ,可能会出现广泛而活跃的研究热潮以及一些新的特点 .

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National Natural Science Foundation of China [30590381]; Knowledge Innovation Program of the Chinese Academy of Sciences [KZCX2YW-432]; International Partnership Project

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The reaction mechanism of Pd(O)-catalyzed allenes silastannation reaction is investigated by the density functional method B3LYP. The overall reaction mechanism is examined. For the allene insertion step, the Pd-Si bond is preferred over the Pd-Sn bond. The electronic mechanism of the allene insertion into Pd-Si bond to form sigma-vinylpalladium (terminal-insertion) and sigma-allylpalladium (internal-insertion) insertion products is discussed ill terms of the electron donation and back-donation. It is found that the electron back-donation is significant for both terminal- and internal-insertion. During allene insertion into Pd-Si bond, internal-insertion is preferred over terminal-insertion. By using methylallene, the regio-selectivity for the monosubstituted allene insertion into Pd-Si and Pd-Sn bond is analyzed.

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Enantiomerically pure dinuclear ruthenium complexes with 1,2-dicarbonylhydrazide as a bridging ligand are optically active in the visible and near infrared spectral regions depending on the oxidation states of the metal centers and are useful as an electrochemically driven near infrared chiroptical switch.

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Active site structure for NO decomposition carried out on perovskite-like oxides were discussed based on the N-2 yield measured from LaSrNi1-x,AlxO4 with different B-site cations and from La2-ySryCuO4 with different crystal phases. Results show that the active site contains two oxygen vacancies, two transition metals, and one lattice-oxygen, with the oxygen vacancy locating on the apex of MO6 octahedron, and the lattice oxygen locating between the two transition metals (i.e., M-O-M plane). Density functional theory (DFT) analysis to the structure shows that this new active site is the most active structure for NO adsorbing, and hence, for NO decomposition. The similar trend of the relative energies that are required for the formation of oxygen vacancies with f form (calculated from DFT), the amount of oxygen vacancies, and the activities (N-2 yield) certifies this result further.

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Vacuum ultraviolet excitation spectra of phosphors (La,Gd)PO4:RE3+ (RE = Eu or Tb) and X-ray photoelectron spectra of LaPO4 and GdPO4 are investigated. The vacuum ultraviolet excitation intensity of (La,Gd)PO4:RE3+ is enhanced with the increasing of Gd3+ content, which implies that Gd3+ plays an intermediate role in energy transfer from host absorption band to RE3+. When Gd3+ is doped into LaPO4:Eu, charge transfer band (CT band) begins to shift to higher energy region and the overlap degree of CT band and the host absorption band gets greater with more Gd3+ doped into LaPO4. These results suggest that the dopant (Gd3+) gives an important influence on energy transfer efficiency. The top of LaPO4 valance band is formed by the 2p level of O2-, whereas that of GdPO4 valance band is formed by the 2p level of O2- and the 4f level of Gd3+, showing the differences in band structures between LaPO4 and GdPO4.

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Nanometer-scale plowing friction and wear of a polycarbonate thin film were directly measured using an atomic force microscope (AFM) with nanoscratching capabilities. During the nanoscratch tests, lateral forces caused discrepancies between the maximum forces for the initial loadings prior to the scratch and the unloading after the scratch. In the case of a nanoscratch test performed parallel to the cantilever probe axis, the plowing friction added another component to the moment acting at the cantilevered end compared to the case of nanoindentation, resulting in an increased deflection of the cantilever. Using free-body diagrams for the cases of nanoindentation and nanoscratch testing, the AFM force curves were analyzed to determine the plowing friction during nanoscratch testing. From the results of this analysis, the plowing friction was found to be proportional to the applied contact force, and the coefficient of plowing friction was measured to be 0.56 +/- 0.02. Also, by the combination of nanoscratch and nanoindentation testing, the energetic wear rate of the polycarbonate thin film was measured to be 0.94 +/- 0.05 mm(3)/(N m).