48 resultados para Tarakanova, Elizaveta, 1745-1775
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通过选择性富集培养,从辽河油田稠油污染土壤4号土样中,获得了能以高浓度菲(2000 mg·L-1)为唯一碳源和能源快速生长的优势菌系和优良菌株ZL5.16S rDNA核苷酸序列分析表明,ZL5菌株归类于鞘氨醇单胞菌属.分得的菌系和菌株有较强的降解菲能力,120 h混合菌系降解了投加菲的95.28%,菌株降解了69.24%,但它们对芘的降解能力均较低.外加碳源葡萄糖可提高菌系和菌株的菲、芘降解能力,加量多,提高幅度大,但超过一定量,降解速率开始下降,表现出抑制效应.所以,应用时需控制适宜的浓度.
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稳定性核素示踪是现代农业研究中一门新兴技术。稳定性核素15N作为一种有效手段在农业施肥研究、氮素循环研究中发挥着极为重要的作用。本文介绍了15N的相关概念,列举了20世纪80年代以来15N在氮肥研究、氮素转化研究以及农业环境保护中的应用进展,阐明了应用15N的新技术已解决的问题,以及将要解决的问题,并展望了性核素示踪技术的应用前景。
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研究了外源NO和ABA对杨树气孔运动调节作用 .结果表明 ,外源NO和ABA都能诱导杨树离体叶片气孔关闭 ,且具有剂量效应 ,NO可加强ABA诱导气孔关闭的作用 .NO清除剂 (c PTIO)可大大减弱NO和ABA对气孔关闭的诱导作用 .证实了NO参与ABA调控气孔开闭运动过程 ,不同浓度NO供体SNP和ABA处理杨树离体叶片 ,SOD活性变化不明显 ,POD活性受到显著抑制 .杨树叶片粗酶液的体外实验表明 ,不同浓度SNP对POD活性的抑制呈明显的浓度及时间效应 ;而ABA对POD活性则几乎没有影响 .本研究证明 ,NO调节ABA诱导的树木气孔关闭作用 ,是ABA诱导树木气孔关闭的一种重要信号分子 .
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该文以长白山阔叶红松林为研究对象,以Raupach提出的Localized Near Field(LNF)理论为依据,耦合垂直速度标准差σw(z)和拉格朗日时间尺度TL(z),建立林冠内水汽源/汇强度和平均浓度廓线之间的关系;利用拉格朗日反演模型提出了通过林冠水汽浓度梯度计算林冠内的水汽源/汇强度进而推算森林蒸散的方法.模拟结果与开路涡动相关系统的观测数据比较显示:白天水汽累积通量的模拟精度达到81%,模拟值高出实测值约15%~25%;夜间模拟值比实测值高出2~4倍,其原因尚不清楚.观测期内全天水汽总量模拟值298.91 mm,观测值为240.33 mm.最后,讨论了水汽源/汇强度及其通量随时间和高度的演变过程.
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Magnetite dodecahedral nanocrystals were fabricated using ethlenediamine tetraacetic acid (EDTA)-mediated hydrothermal route. Scanning electron microscopy images displayed that the products were almost dodecahedrons. The length of two different ribs were about 300 and 200 nm, respectively. X-ray diffraction patterns showed that the products were the cubic inverse spinel structure. Fourier transform infrared spectrum directly provided evidence of the EDTA bound to a specific surface of the precipitated magnetic nanocrystal.
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Magnetically functionalized mesoporous silica spheres with different size (average diameter, A.D.) from 150 nm to 2 mu m and pore size distribution were synthesized by generating magnetic FexOy nanoparticles onto the mesoporous silica hosts using the sol-gel method. The X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), N-2 adsorption/desorption results show that these composites conserved regular sphere morphology and ordered mesoporous structure after the formation of FexOy nanoparticles. XRD and X-ray photoelectron spectroscopy (XPS) analysis confirmed that the FexOy generated in these mesoporous silica hosts is mainly composed of gamma-Fe2O3. Magnetic measurements reveal that these composites with different gamma-Fe2O3 loading amounts possess super-paramagnetic properties at 300 K, and the saturation magnetization increases with increasing Fe ratio loaded.
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Single-walled carbon nanotubes (SWNTs) can selectively induce human telomeric i-motif DNA formation at pH 7.0. Based on this property, we design a DNA nanomachine induced by SWNTs on gold surface. The motor DNA is human telomeric G-quadruplex DNA. The reversible hybridization between the motor DNA and its complementary human telomeric i-motif DNA can be modulated by SWNTs without changing solution pH. Up to now, to our knowledge, there is no report to show that a DNA nanomachine is induced by SWNTs or a DNA nanomachine can detect i-motif formation at pH 7.0. Our work may provide a new concept for designing an SWNT-induced DNA nanomachine and for the detection of i-motif DNA structure at pH 7.0. DNA hybridization, conformational transition and i-motif formation have been characterized on surface or in solution by fluorescence confocal microscopy, circular dichroism, DNA melting and gel electrophoresis. The folding and unfolding kinetics of the DNA nanomachine on gold surface were studied by Fourier transform-surface plasmon resonance (FT-SPR). All these results indicate that SWNTs can induce the DNA nanomachine to work efficiently and reversibly.
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LiBa2B5O10:RE3+ (RE = Dy, Tb and Tm) was synthesized by the method of high-temperature solid-state reaction and the thermoluminescence (TL) properties of the samples under the irradiation of the gamma-ray were studied. The result showed that Dy3+ ion was the most efficient activator. When the concentration of Dy3+ was 2 mol%, LiBa2B5O10:Dy3+ exhibited a maximum TL output. The kinetic parameter of LiBa2B5O10:0.02Dy was estimated by the peak shape method, for which the average activation energy was 0.757 eV and the frequency factor was 1.50 x 10(7) s(-1). By the three-dimensional (3D) TL spectrum, the TL of the sample was contributed to the characteristic f-f transition of DY3+. The dose-response of LiBa2B5O10:0.02Dy to gamma-ray was linear in the range from 1 to 1000 mGy. In addition, the decay of the TL intensity of LiBa2B5O10:0.02Dy was also investigated.
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Novel poly(ester carbonate)s were synthesized by the ring-opening polymerization Of L-lactide and functionalized carbonate monomer 9-phenyl-2,4,8,10-tetraoxaspiro[5,5]undecan-3-one derived from pentaerythritol with diethyl zinc as an initiator. H-1 NMR analysis revealed that the carbonate content in the copolymer was almost equal to that in the feed. DSC results indicated that T-g of the copolymer increased with increasing carbonate content in the copolymer. Moreover, the protecting benzylidene groups in the copolymer poly(L-lactide-co-9-phenyl-2,4,8,10-tetraoxaspiro[5,5]undecan-3-one) were removed by hydrogenation with palladium hydroxide on activated charcoal as a catalyst to give a functional copolymer, poly(L-lactide-co-2,2-dihydroxylmethyl-propylene carbonate), containing pendant primary hydroxyl groups. Complete deprotection was confirmed by H-1 NMR and FTIR spectroscopy. The in vitro degradation rate of the deprotected copolymers was faster than that of the protected copolymers in the presence of proteinase K. The cell morphology and viability on a copolymer film evaluated with ECV-304 cells showed that poly(ester carbonate)s derived from pentaerythritol are good biocompatible materials suitable for biomedical applications.
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Sandwich-like heteropoly molybdochromophosphates of supermolecular compound [NH3(CH2)(6)NH3](2)H-3{Cr[Mo6O15(HPO4)(H2PO4)(3)](2)}. 4H(2)O has been hydrothermally synthesized and the single crystal structure has been determined by X-ray diffraction. The crystal data are has follows: triclinic, space group P (1) over bar a=12.156(2), b=12.809(3), c=13.530(3) Angstrom, alpha=102.46(3)degrees, beta=93.67(3)degrees, gamma=93.46(3)degrees, V=2046.9(7) Angstrom(3), Z=1, M-r=2768.69, D-c=2.246 g/cm(-3), F(000)=1337, mu=2.162 mm(-1). The structure has been refined to R=0.0666 and wR=0.1745 by full-matrix least-squares method. The title compound is composed of 1, 6-diaminohexane, water molecules, and {Cr[Mo6O15(HPO4)(H2PO4)(3)](2)}(7-) anion which consists of six oxygen atoms from two [Mo6P4] units with a sandwich-like transition metal atom Cr located at the center of symmetry.
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The curing temperature, pressure, and curing time have significant influence on finished thermosetting composite products. The time of pressure application is one of the most important processing parameters in the manufacture of a thermosetting composite. The determination of the time of pressure application relies on analysis of the viscosity variation of the polymer, associated with curing temperature and curing time. To determine it, the influence of the time of pressure application on the physical properties of epoxy-terminated poly(phenylene ether ketone) (E-PEK)-based continuous carbon fiber composite was studied. It was found that a stepwise temperature cure cycle is more suitable for manufacture of this composite. There are two viscosity valleys, in the case of the E-PEK system, associated with temperature during a stepwise cure cycle. The analysis on the effects of reinforcement fraction and defect content on the composite sheet quality indicates that the width-adjustable second viscosity valley provides a suitable pressing window. The viscosity, ranging from 400 to 1200 Pa . s at the second viscosity valley, is the optimal viscosity range for applying pressure to ensure appropriate resin flow during curing process, which enables one to get a finished composite with optimal fiber volume fraction and low void content. (C) 1997 John Wiley & Sons, Inc.
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The conformation of phenyl rings in the side groups of the helical chain polymer poly(tripenyl-methyl methacrylate) (1) in solution was studied by spectroscopic methods. According to the Raman spectrum the phenyl rings of 1 and triphenylmethyl methacrylate in solution have the same depolarization ratio at 1002 cm-1. The electronic spectra (ultraviolet and fluorescence) of 1 are similar to those of model substances, except for the "red shift" of the spectra of about 5 nm. It was concluded that the phenyl rings can rotate around the phenyl-C bond.
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Based on the Navier-Stokes equation, an equation describing the Langmuir circulation is derived by a perturbation method when the influences of Coriolis force and buoyancy force are both considered. The approach used in the analysis is similar to the works carried out by Craik and Leibovich [J. Fluid Mech. 73 (1976) 401], Leibovich [J. Fluid Mech. 79 (1977) 715] and Huang [J. Fluid Mech. 91 (1979) 191]. Potential applications of the equation proposed are discussed in the area of Antarctic circumpolar current.
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蓝子鱼科鱼类隶属于鲈形目、刺尾鱼亚目,广泛分布于我国东海、南海及台湾海域。本文根据中国科学院海洋研究所多年来在我国海域采集并收藏的以及部分补充采集的蓝子鱼标本,参考国际最新研究资料,对我国海域蓝子鱼科鱼类进行分类和动物地理学研究,共记录中国海域蓝子鱼科鱼类1属2亚属11种。经研究分析,得到如下结论: 1.中国沿海蓝子鱼科鱼类的多样性问题。国内曾有13种蓝子鱼的分布记录,其中蠕纹蓝子鱼Siganus vermiculatus和暗体蓝子鱼S. punctatissimus仅以前的学者做过名录形式的记载,并无标本收藏,本文中不做介绍。此外尖嘴蓝子鱼Siganus unimaculatus也可能存在于中国海域,有待于进一步研究。目前确定在中国海域有分布的蓝子鱼为11种,约占世界总种数(27)的40%多,种的多样性较高。 2. 形态学比较研究说明,蓝子鱼在体形、体色、牙齿、头骨、椎骨、耳石等特征方面存在种间差异,可作为蓝子鱼科鱼类分类的有效鉴别特征。对于外部形态极其相似的种,可借助内部解剖特征相辅助予以区分。 3.对蓝子鱼动物地理学特点研究分析结论如下:a.中国海域存在的11种蓝子鱼在印度-太平洋海域均有分布,没有地方特有种。b.长鳍蓝子鱼和褐蓝子鱼在我国东海、台湾海域和南海均有分布,褐蓝子鱼在黄海北部亦有分布,种群数量较大;其它9种,除凹吻蓝子鱼仅分布于南海外,均分布于南海及台湾海域,种群数量较小。c.中国海域蓝子鱼种类组成与邻近的菲律宾、马来西亚、印度尼西亚海域比较相似,中国分布的种类在这些海域均有分布,且分布于这一区域而中国没有记录的有5种。与日本相比,种类组成也比较相似,中日共有种达9种,仅分布于中国海域2种,仅分布于日本海域1种。 4. 作者参照国际最新研究结果和较为公认的分类系统Nelson(1994),将蓝子鱼科置于刺尾鱼亚目,而不再使用国内学者长期惯用的蓝子鱼亚目。蓝子鱼科包括一属蓝子鱼属Siganus Forsskål, 1775,两亚属:蓝子鱼亚属Siganus Forsskål, 1775 和罗蓝子鱼亚属 Lo Seale, 1906,同时使全部种名的变动和确定与国际最新研究结果(Woodland, 1990; 2001)取得一致。
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本文概述了图象压缩编码的原理和方法,并提出了一种改进的基于方向分解的图象压缩编码方法,实验结果表明,对于一般的室内和室外的景物图象,当压缩比高达50 :1时,其恢复图象的视觉效果仍然较好。