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显示中耳和内耳细微结构的标准化标本制作方法
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作者 王乃利 张迪 +4 位作者 穆瑞民 寇印华 曹承刚 马超 刘克 《解剖学报》 CAS CSCD 北大核心 2018年第6期830-833,共4页
目的探索显示中耳和内耳细微结构直视标本的标准化制作方法。方法使用人颞骨材料,在颅内和颅底面画出标准锯路的标志线,选择细齿窄条钢弓锯,沿标志线锯开颞骨显示中耳结构。再用手握式玉石磨钻分别研磨显示内耳结构。最后完成对鼓膜、... 目的探索显示中耳和内耳细微结构直视标本的标准化制作方法。方法使用人颞骨材料,在颅内和颅底面画出标准锯路的标志线,选择细齿窄条钢弓锯,沿标志线锯开颞骨显示中耳结构。再用手握式玉石磨钻分别研磨显示内耳结构。最后完成对鼓膜、听小骨、面神经、鼓索神经和颈内动脉等结构的仿真复原,并用合页连结锯开的两半颞骨。结果在锯开的颞骨内可清晰显示中耳鼓室的6个壁,以及锥状隆起、咽鼓管、前庭窗和蜗窗等细微结构。磨制后的内耳可见3个打开的骨半规管和耳蜗的剖面。复原后的听骨链、面神经、鼓索神经、颈内动脉和鼓膜等结构,均以三维方式显示原有结构的特征和位置关系。由合页连结的颞骨标本,既可打开观察内部结构,也可合拢显示整体形态。结论采用锯开和研磨技术制作耳标本可以取得满意的结果,标准化的锯路标志和标准的定位研磨是成功制作的关键。 展开更多
关键词 中耳 内耳 解剖学 标本制作
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Isolation and algae-lysing characteristics of the algicidal bacterium B5 被引量:30
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作者 mu rui-min FAN Zheng-qiu +3 位作者 PEI Hai-yan YUAN Xue-liang Liu Si-xiu WANG Xiang-rong 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2007年第11期1336-1340,共5页
Water blooms have become a worldwide environmental problem. Recently, algicidal bacteria have attracted wide attention as possible agents for inhibiting algal water blooms. In this study, one strain of algicidal bacte... Water blooms have become a worldwide environmental problem. Recently, algicidal bacteria have attracted wide attention as possible agents for inhibiting algal water blooms. In this study, one strain of algicidal bacterium B5 was isolated from activated sludge. On the basis of analysis of its physiological characteristics and 16S rDNA gene sequence, it was identified as Bacillusfusiformis. Its algaelysing characteristics on Microcystis aeruginosa, Chlorella and Scenedesmus were tested. The results showed that: (1) the algicidal bacterium B5 is a Gram-negative bacterium. The 16S rDNA nucleotide sequence homology of strain B5 with 2 strains of B. fusiformis reached 99.86%, so B5 was identified as B. fusiformis; (2) the algal-lysing effects of the algicidal bacterium B5 on M. aeruginosa, Chlorella and Scenedesrnus were pronounced. The initial bacterial and algal cell densities strongly influence the removal rates of chlorophyll-a. The greater the initial bacterial cell density, the faster the degradation of chlorophyll-a. The greater the initial algal cell density, the slower the degradation of chlorophyll-a. When the bacterial cell density was 3.6 × 10^7 cells/ml, nearly 90% of chlorophyll-a was removed. When the chlorophyll-a concentration was less than 550 μg/L, about 70% was removed; (3) the strain B5 lysed algae by secreting metabolites and these metabolites could bear heat treatment. 展开更多
关键词 algicidal bacteria water blooms algae-lysing characteristic 16S rDNA Bacillusfusiformis
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Alga-lysing bioreactor and dominant bacteria strain 被引量:3
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作者 PEI Hai-yan HU Wen-rong +1 位作者 mu rui-min LI Xiao-cai 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2007年第5期546-552,共7页
Alga-lysing bacteria have been paid much attention to in recent years. In this study, the alga-lysing strain P05 which was isolated from an immobilizing biosystem was immobilized by coke and elastic filler, forming tw... Alga-lysing bacteria have been paid much attention to in recent years. In this study, the alga-lysing strain P05 which was isolated from an immobilizing biosystem was immobilized by coke and elastic filler, forming two biological reactors. The removal efficiencies of algae, NH4^+-N and organic matter using the two reactors were studied. The results showed that strain P05 was an ideal algal-lysing bacteria strain because it was easy to be immobilized by coke and elastic filler which are of cheap, low biodegradability and the simple immobilization procedure. After 7 d filming, the biological film could be formed and the reactors were used to treat the eutrophic water. These two reactors were of stability and high effect with low cost and easy operation. The optimal hydraulic retention time (HRT) of each reactor was 4 h. The algae removal rates were 80.38% and 82.1% (in term of Chl-α) of coke reactor and filler reactor, respectively. And that of NH4^+-N were 52.3% and 52.7%. The removal rates of CODMn were 39.03% and 39.64%. The strain P05 was identified as Bacillus sp. by PCR amplification of the 16S rRNA gene, BLAST analysis, and comparison with sequences in the GenBank nucleotide database. 展开更多
关键词 alga-lysing algae removal IMMOBILIZATION 16S rRNA Bacillus sp.
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