23 resultados para Laboratory analysis

em Chinese Academy of Sciences Institutional Repositories Grid Portal


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采用野外典型抽样调查和室内分析测定的方法,在黄土丘陵半干旱区-安塞水土保持综合试验站研究了退化刺槐林经萌蘖更新和重造侧柏林改造后林地土壤水分含量、乔木根系生物量和生物多样性指标的差异。结果表明:萌蘖更新林地内的土壤水分含量和生物多样性指数均高于重造侧柏林地;不同改造方式下整个土层内根系生物量的差异较大,根系生物量最大的是重造侧柏林地,为17.59 g,最小的是退化刺槐林,为16.59 g。萌蘖刺槐林与退化刺槐林相比,土壤水分含量和生物多样性指数变化不大,但林内乔木种类较退化刺槐林内丰富。因此利用间伐萌蘖方式对退化刺槐林改造是可行的。

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采用盆栽试验与室内分析相结合的方法,研究了6种低分子有机酸和一种有机酸盐对辣椒生长发育和叶片活性氧代谢的影响。结果表明:柠檬酸、乙酰丙酸和有机酸钾处理不仅可显著提高辣椒根系干质量,增加辣椒vC含量,而且提高了辣椒的产量。甲酸、柠檬酸、乙酰丙酸和有机酸钾处理使根系活力比对照分别提高83%、93.8%、96.75%和99.5%。柠檬酸、乙酰丙酸和有机酸钾处理提高了辣椒叶片的SOD和POD活性,降低了膜脂过氧化产物MDA含量,延缓了叶片衰老。但是低分子有机酸处理对CAT活性的影响较小。

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通过野外调查和室内分析,采用多元线性逐步回归和地理信息系统(GIS)相结合的方法,研究了黄土丘陵区燕沟流域表层(0~20 cm)土壤的有机碳密度、空间分布及其与土地利用类型和地形因子等的关系。结果表明,流域表层土壤有机碳密度平均为1.72 kg/m2,变幅为0.97~2.93 kg/m2;土地利用类型是影响土壤有机碳密度变化的首要因子;流域土壤有机碳密度呈镶嵌的树枝状和条带状空间分布格局,其高值斑块区与乔木林地和灌木林地的分布一致,中值斑块区与草地和川坝地的分布一致,低值斑块区与梯田、果园、坡耕地、疏林地和未成林地的分布一致。流域表层土壤有机碳总储量为76.81×103t。

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通过野外考察与室内分析相结合 ,对大巴山北坡不同海拔高度的土壤特性进行研究 ,确定了各剖面的诊断层和诊断特性及其在系统分类中的位置。结果表明大巴山北坡各垂直带土壤在系统分类中可划归 2个土纲的 6个土类 ,系统分类中土壤的分类位置与发生分类位置并不具有简单的一一对应的关系。

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通过野外调查和室内分析相结合的方法,研究子午岭次生林区不同土地利用方式下的土壤性质状况,分析土地利用状况与土壤质量之间的关系,结果表明:不同土地利用方式表层土壤有机质、全氮、全磷、pH值、脲酶、蔗糖酶和碱性磷酸酶含量或活性差异显著,农地主要土壤养分含量和酶活性较低,林地则较高。除pH值外,不同利用方式下土壤养分和酶活性均随土层深度的增加而逐渐减小。除土壤pH值外,不同利用方式下土壤有机质、全氮、全磷、铵态氮、脲酶、蔗糖酶、碱性磷酸酶和过氧化氢酶之间呈显著或极显著正相关性。以林地为对照的土壤退化指数表明农用地和撂荒翻耕地土壤质量退化显著,其表层(0~20cm)土壤退化指数分别为44.86%和43.10%;撂荒未翻耕地深层(20~130cm)土壤质量则有所提高。

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Based on amount of field investigation and laboratory analysis, this paper emphasized on the establishment of soil improvement benefit evaluation models. It is pointed out that the benefit evaluation models can be simulated by taking litter biomass, mean diameter of breast high (D), mean height (H) and (D 2H) as independent variables and taking comprehensive benefit evaluation index as dependent variable. The models vary with different independent variables and can be chosen to use according to actual situation.

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The nutrient cycling in the reed field has been studied via field investigation and laboratory analysis. The results indicate that N absorption in higher reed productvity field is 0.6044% (high level); The P absorption is 0.1100% (intermediate); The K absorption is 0.0153% (low level).the cycling coefficiencies for N,P and K are 0.16、 0.15 and 0.12,respectively. They are all at low levels.

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Plankton communities in eight lakes of different trophic status near Yangtze, China were characterized by using denatured gradient gel electrophoresis (DGGE). Various water quality parameters were also measured at each collection site. Following extraction of DNA from plankton communities, 16S rRNA and 18S rRNA genes were amplified with specific primers for prokaryotes and eukaryotes, respectively; DNA profiles were developed by DGGE. The plankton community of each lake had its own distinct DNA profile. The total number of bands identified at 34 sampling stations ranged from 37 to 111. Both prokaryotes and eukaryotes displayed complex fingerprints composed of a large number of bands: 16 to 59 bands were obtained with the prokaryotic primer set; 21 to 52 bands for the eukaryotic primer set. The DGGE-patterns were analyzed in relation to water quality parameters by canonical correspondence analysis (CCA). Temperature, pH, alkalinity, and the concentration of COD, TP and TN were strongly correlated with the DGGE patterns. The parameters that demonstrated a strong correlation to the DGGE fingerprints of the plankton community differed among lakes, suggesting that differences in the DGGE fingerprints were due mainly to lake trophic status. Results of the present study suggest that PCR-DGGE fingerprinting is an effective and precise method of identifying changes to plankton community composition, and therefore could be a useful ecological tool for monitoring the response of aquatic ecosystems to environmental perturbations.

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In this study, the immunoglobulin M heavy chain gene of European eel (Anguilla anguilla) was cloned and analyzed. The full-length cDNA of the IgM heavy chain gene (GenBank accession no. EF062515) has 2089 nucleotides encoding a putative protein of 581 amino acids. The IgM heavy chain was composed of leader peptide (L), variable domain (VH), CH1, CH2. Hinge, CH3, CH4, and C-terminus and two novel continuous putative N-glycosylation sites were found close to the second cysteine of CH3 in A. anguilla-H1 and A. anguilla-H2. The deduced amino acid sequence of the European eel IgM heavy chain constant region shared similarities to that of the Ladyfish (Elops saurus). Atlantic salmon (Salmo salar), rainbow trout (Oncorhynchus mykiss), Grass carp (Ctenopharingodon idella), Common carp (Cyprinus carpio), Channel catfish (Ictalurus punctatus), and the orange-spotted grouper (Epinephelus coioides) with the identity of 46.1%, 39.7%, 38.9%, 32.4%, 32.3%, 31.7%, and 30.7%, respectively. The highest level of IgM gene expression was observed in the kidney, followed by the spleen, gills, liver, muscle and heart in the apparently healthy European eels. (C) 2008 Elsevier B.V. All rights reserved.

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Lake Dianchi is in Yunnan Province in southwestern China. In recent years, significant cyanobacterial blooms have occurred in this lake nearly every year because of eutrophication. Monitoring data for the past 5 years acquired by our research group showed that phytoplankton composition alternated between species of Microcystis sp. during warm seasons and those of Aphanizomenon sp. during cool seasons. In March 2003, when phytoplankton composition was highly dominated by Aphanizomenon sp., samples were taken from the lake for toxin detection and immediate strain isolation. A mouse bioassay with extracts from the lyophilized field material showed obvious intoxication from paralytic shellfish poisons (PSPs), and all mice died within 30 min. Further analysis of both field and isolated algal strain Aphanizomenon DC-1 by the postcolumn HPLC-FLD method confirmed its PSP-producing ability The analogues found in the extracts from the field material were neoSTX, dcSTX, and dcGTX3, with contents of 2.279, 1.135, and 0.547 ng/mg DW, respectively. Under laboratory culture condition, toxin content in the Aphanizomenon strain DC-1 varied greatly during different growth phases, with two peaks: in the early-exponential and late-stationary growth phases. When the culture grew at a relatively high rate during the mid- to late-exponential growth phase, toxin content declined gradually. Moreover, the types of toxin in the DC-1 strain varied greatly during a single culture cycle. The HPLC results showed that dcSTX was the only toxin isomer detected throughout the culture period, and its level remained stable. On the other hand, dcGTX2 and GTX4 were the major toxins during the early-exponential and stationary phases, respectively. This article presents the first data on the identification and detection of paralytic shellfish toxins from cyanobacteria in Lake Dianchi. As far as we know, this is also the first report of this type of toxin in inland water bodies in China. Our study indicates the threat associated with PSP toxins in Lake Dianchi and suggests that necessary measures and programs for control are urgently needed to prevent the spread of toxic cyanobacterial blooms. (c) 2006 Wiley Periodicals, Inc.

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Current-based microscopic defect analysis method such as current deep level transient spectroscopy (I-DLTS) and thermally stimulated current have been developed over the years at Brookhaven National Laboratory (BNL) for the defect characterizations on heavily irradiated (Phi(n) >= 10(13) n/cm(2)) high-resistivity (>= 2 k Omega cm) Si sensors/detectors. The conventional DLTS method using a capacitance transient is not valid on heavily irradiated high-resistivity Si sensors/detectors. A new optical filling method, using lasers with various wavelengths, has been applied, which is more efficient and suitable than the traditional voltage-pulse filling. Optimum defect-filling schemes and conditions have been suggested for heavily irradiated high-resistivity Si sensors/detectors. (c) 2006 Published by Elsevier Ltd.

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Current-based microscopic defect analysis method such as current deep level transient spectroscopy (I-DLTS) and thermally stimulated current have been developed over the years at Brookhaven National Laboratory (BNL) for the defect characterizations on heavily irradiated (Phi(n) >= 10(13) n/cm(2)) high-resistivity (>= 2 k Omega cm) Si sensors/detectors. The conventional DLTS method using a capacitance transient is not valid on heavily irradiated high-resistivity Si sensors/detectors. A new optical filling method, using lasers with various wavelengths, has been applied, which is more efficient and suitable than the traditional voltage-pulse filling. Optimum defect-filling schemes and conditions have been suggested for heavily irradiated high-resistivity Si sensors/detectors. (c) 2006 Published by Elsevier Ltd.

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This paper describes the design and fabrication process of a two-dimensional GaAs-based photonic crystal nanocavity and analyzes the optical characterization of cavity modes at room temperature. Single InAs/InGaAs quantum dots (QDs) layer was embedded in a GaAs waveguide layer grown on an Al0.7Ga0.3As layer and GaAs substrate. The patterning of the structure and the membrane release were achieved by using electron-beam lithography, reaction ion etching, inductively coupled plasma etching and selective wet etching. The micro-luminescence spectrum is recorded from the fabricated nanocavities, and it is found that some high-order cavity modes are clearly observed besides the lowest-order resonant mode is exhibited in spite of much high rate of nonradiative recombination. The variance of resonant modes is also discussed as a function of r/a ratio and will be used in techniques aimed to improve the probability of achieving spectral coupling of a single QD to a cavity mode.

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Affinity chromatography is unique among separation methods as it is the only technique that permits the purification of proteins based on biological functions rather than individual physical or chemical properties. The high specificity of affinity chromatography is due to the strong interaction between the ligand and the proteins of interest. Membrane separation allows the processing of a large amount of sample in a relatively short time owing to its structure, which provides a system with rapid reaction kinetics. The integration of membrane and affinity chromatography provides a number of advantages over traditional affinity chromatography with porous-bead packed columns, especially with regard to time and recovery of activity. This review gives detailed descriptions of materials used as membrane substrates, preparation of basic membranes, coupling of affinity ligands to membrane supports, and categories of affinity membrane cartridges. It also summarizes the applications of cellulose/glycidyl methacrylate composite membranes for proteins separation developed in our laboratory. (C) 2001 Elsevier Science B.V. All rights reserved.