利用分光光度计测量光学晶体的折射率

晶体折射率的准确测定是晶体上薄膜器件设计的基础。介绍了利用分光光度计测量晶体折射率的方法，通过背面影响系数法、背面镀增透膜和将两者结合起来的方法消除晶体反射率测量时背面反射带来的影响，给出了具体的步骤并对测量误差进行了分析。由于晶体的光学各向异性，采用起偏器扫描的方法测量晶体光学性质随方向的变化。通过对LiB3P5晶体的折射率的测量，证实了该方法的可行性并可用于其他光学晶体折射率的测量。

La separación y el conflicto parental: efectos en las relaciones afectivas de los hijos adultos jóvenes.

323 p.

O Barão de Lavos: do belo ao grotesco: uma análise comparativista

Esta pesquisa tem por objetivo, em perspectiva comparada, analisar o encontro de duas artes: a literatura e a pintura, observado na obra O Barão de Lavos (1891), de Abel Botelho. O romance naturalista, com traços decadentistas, do escritor Abel Botelho que abre a série intiulada Patologia Social (1891) nos mostra, como diz José Carlos Seabra Pereira, um tempo em se convegiam o romantismo,o realismo e pretensões de modernidade baudealiriana (mais ou menos satanistas) (PEREIRA, 1995) e onde as diversas categorias das artes se encontram e se conjugam. Nesse cenário caótico, mas profícuo, temos este romance que estabelece a arte plástica como ponto focal dentro do texto. Analisa, sobretudo, o processo da escrita onde foi possível constatar a deformação do belo em grotesco ao longo do romance. Investiga a questão imagética encontrada no texto botelhiano, caracterizada através da gravura Rapto de Ganimedes; litografia de grande simbologia dentro dessa obra literária, pois representa o ideal estético idealizado pelo próprio Barão, e tudo de significativo que compõe a trajetória e as emoções de D. Sebastião ao longo de sua vida, portanto permeando e atravessando toda narrativa

毛冠菊属的系统学研究

　　毛冠菊属是菊科21个“有问题”属中的一个，主要分布于青藏高原地区。按照林镕、陈艺林的概念，它包含了Nannoglottis、．Stereosanthus、Vierhapperia、Senecio和Doronicum5个属的成员。它曾先后被放入旋覆花族、千里光族和紫菀族，在上述三族中的亚族位置也不确定。它的许多重要性状，如舌片颜色、染色体数目等等，人们所知甚少。由于缺乏野外工作以及看不到大多数名字的模式，林镕、陈艺林对该属的修订有待深入的研究。本文研究了该属的外部形态学、微形态学、解剖学、孢粉学、细胞学、生态学以及ITS序列，确定了毛冠菊属的分类位置，并建立了一个新的属下分类系统。 1．外部形态 在检查大量标本（包括大多数模式）和野外居群考察的基础上，分析了主要外部形态学性状的变异式样及其对划定物种范围的价值。共确认以下9个种：青海毛冠菊、厚毛毛冠菊、狭舌毛冠菊、虎克毛冠菊、宽苞毛冠菊、大果毛冠菊、毛冠菊、玉龙毛冠菊和云南毛冠菊。川西毛冠菊被处理成狭舌毛冠菊的异名。 2．微形态学 在光镜下检查了毛冠菊属9种和紫菀族2个代表属的花柱的形状、花药顶端不育附属物、花药基部、花药基部、花盘、花丝领、药室内壁细胞等微形态性状。除了花柱基外，其他的微形态学在属内一致。管状花的花柱形态支持将毛冠菊属放在紫菀族，但其药室内壁细胞两极加厚式样表明它和广义的旋覆花有某些联系。 3．叶表皮研究 在光镜和电镜下检查了毛冠菊属8个种的叶表皮特征。．所有种的气孔器都为不规则型。青海毛冠菊表皮细胞的为多边形，而其他种都为不规则型。青海毛冠菊表皮角质层的加厚方式也与其他种明显不同。 4．扫描电镜下的舌片和花柱分枝特征 在扫描电镜下观察毛冠菊属8种和紫菀族7个代表种的舌片近轴面表皮细胞。发现毛冠菊属的舌片近轴面表皮细胞都为板状，并且沿细胞中央特征性加厚，这与紫菀族类型的表皮细胞一致，但毛冠菊属表皮细胞的角质层主要是纵向条纹或皱纹，而紫菀族总是横向的条纹或皱纹，明显不同。 在扫描电镜下又检查了毛冠菊属8种和紫菀族8个代表种的管状花花柱分枝近轴面的结构，结果在毛冠菊属管状花花柱分枝的近轴面都发现了柱头毛状的突起，而在紫菀族8种中没有发现。从突起的形状和位置判断，它可能是残存的、未充分发育的柱头毛。这表明雌性不育管状花可能刚刚从两性管状花演化而来。 也在扫描电镜下观察了毛冠菊属6种和紫菀族8个代表种的舌状花和丝状花的花柱分枝的远轴面，结果在毛冠菊属4种中发现了类似扫集毛状的突起。从这种突起的位置和形状判断，它可能是残余的扫集毛。这种突起在除雏菊以外的其他紫菀族代表种中缺失。 5．细胞学 检查了毛冠菊属8种的细胞学性状。结果发现毛冠菊属所有种的染色体基数都为x -9。染色体长度大约4um-lOum。核型公式：毛冠菊、厚毛毛冠菊、狭舌毛冠菊、宽苞毛冠菊和云南毛冠菊都为2n=14m+2sm+2st;玉龙毛冠菊、大果毛冠菊和青海毛冠菊都为2n=12m+4sm+2st。A1、A2值在属内没有明显差异。所有种的核型都是2A型。这表明在物种形成的过程中没有多倍化参与，毛冠菊属宜放在紫菀族而不是千里光族。细胞学证据支持毛冠菊属为一单系类群。 6．分子生物学 测定了毛冠菊属7种的ITS序列，并从基因库里下载了46个ITS序列，涵盖紫菀族14个亚属和旋覆花族、春黄菊族、金盏菊族。以旋覆花族、春黄菊族、金盏菊族为外类群。简约性分析显示，毛冠菊属在紫菀族中，并有较高的bootstrap值，在紫菀族中处于基部位置。Olearia和Chiliotrichum两个Hinterhuberinae亚族的代表属与毛冠菊属密切相关。在属下系统发育分析中，Olearia和Chiliotrichum被选做外类群。652个性状中，共有7】个信息位点（31个在ITSI，33个在ITS2，7个在5.8S）。简约性分析时只获得一棵最简约树。树上有两个明显的进化支，一支仅有青海毛冠菊一种，另一支包含其他种类。这种分支方式也得到形态学和生态学证据的支持。 7．毛冠菊属的系统学 从上述结果可以看出，毛冠菊属宜放入紫菀族中，在紫菀族中处于基部位置，与Hinterhuberinae亚族关系密切。综合上述研究结果，提出一个新的属下 分类系统： 毛冠菊属的新系统 组I单头组Sect. Monocephala T.G.Gao et YL.Chen Sect nov. 青海毛冠菊Nannoglottis ravida (C.Winkl.)Y.L.Chen 组II毛冠菊组Sect. Nannoglottis 系1．长舌系Ser. Delavayanae Ling et YL.Chen 厚毛毛冠菊Nannoglottis delavayi(Franch.)Ling et Y.L.Chen 狭舌毛冠菊Nannoglottis gynura(C.Winkl.) Ling et YL.Chen 虎克毛冠菊Nannoglottis hookeri (C.B.Clarke ex Hook.f.)Kitam. 宽苞毛冠菊Nannoglottis latisquama Ling et Y.L.Chen 大果毛冠菊Nannoglottis macrocarpa Ling et YL.Chen 系2．短舌系Ser. Nannoglottis 毛冠菊Nannoglottis carpesioides Maxim. 玉龙毛冠菊Nannoglottis hieraciphylla (Hand.-Mzt.)Ling et YL.Chen 云南毛冠菊Nannoglottis yuennanensis (Hand.-Mzt.) Hand.-Mzt.

Synopsis of researcher meeting -- Bottlenose Dolphin Health & Risk Assessment Project, February 22-24, 2005

A meeting was convened on February 22-24, 2005 in Charleston, South Carolina to bring together researchers collaborating on the Bottlenose Dolphin Health and Risk Assessment (HERA) Project to review and discuss preliminary health-related findings from captured dolphins during 2003 and 2004 in the Indian River Lagoon (IRL), FL and Charleston (CHS), SC. Over 30 researchers with diverse research expertise representing government, academic and marine institutions participated in the 2-1/2 day meeting. The Bottlenose Dolphin HERA Project is a comprehensive, integrated, multi-disciplinary research program designed to assess environmental and anthropogenic stressors, as well as the health and long-term viability of Atlantic bottlenose dolphins (Tursiops truncatus). Standardized and comprehensive protocols are being used to evaluate dolphin health in the coastal ecosystems in the IRL and CHS. The Bottlenose Dolphin Health and Risk Assessment (HERA) Project was initiated in 2003 by Dr. Patricia Fair at the National Oceanic and Atmospheric Administration/National Ocean Service/Center for Coastal Environmental Health and Biomolecular Research and Dr. Gregory Bossart at the Harbor Branch Oceanographic Institution under NMFS Scientific Research Permit No. 998-1678-00 issued to Dr. Bossart. Towards this end, this study focuses on developing tools and techniques to better identify health threats to these dolphins, and to develop links to possible environmental stressors. Thus, the primary objective of the Dolphin HERA Project is to measure the overall health and as well as the potential health hazards for dolphin populations in the two sites by performing screening-level risk assessments using standardized methods. The screening-level assessment involves capture, sampling and release activities during which physical examinations are performed on dolphins and a suite of nonlethal morphologic and clinicopathologic parameters, to be used to develop indices of dolphin health, are collected. Thus far, standardized health assessments have been performed on 155 dolphins during capture-release studies conducted in Years 2003 and 2004 at the two sites. A major collaboration has been established involving numerous individuals and institutions, which provide the project with a broad assessment capability toward accomplishing the goals and objectives of this project.

血管收缩因子及其制备方法和在制药中的应用

本发明涉及一种血管收缩因子及其制备方法和在制药中的应用，属于生物医学领域。该血管收缩因子是从中国两栖类动物大蹼铃蟾皮肤中分离得到的分子量为65KDa由3条肽链组成的蛋白质，包括2条相同的轻链和1条重链，轻链的分子量为16KDa，重链的分子量为33KDa，等电点6.2，糖含量17-19％。血管收缩因子轻链的N-端20个氨基酸序列结构是：Phe Ser Asp Leu Gln IleGly Ser Leu Lys Cys Ala Val Ala Ala Tyr Asp Gln Gly Ala；重链的N-端封闭。其制备方法是收集大蹼铃蟾皮肤匀浆液或者皮肤分泌物，离心去除沉淀、收集上清液冷冻干燥，经离子交换，凝胶过滤纯化即可得到。该血管收缩因子具有强烈收缩血管，诱导血小板聚集的活性，可作为制备心血管疾病治疗药物和诊断试剂的应用。

HIV-1慢性感染Jurkat细胞系的建立及其特性研究

目的　建立艾滋病病毒Ⅰ型( HIV21) 慢性感染J urkat 细胞系,研究其生物学特性。方法　参照文献方法改良,建立HIV21 ⅢB慢性感染J urkat 细胞系。其细胞系特性采用以下方法检测:光学显微镜观察细胞形态;流式细胞仪检测HIV21 ⅢB感染细胞的阳性率;噻唑蓝(MTT) 法检测抗病毒药物对慢性感染细胞的毒性作用;酶联免疫吸附试验( EL ISA) 检测药物对慢性感染细胞中病毒复制的影响;合胞体形成方法检测药物对HIV21 ⅢB慢性感染细胞与正常细胞融合的阻断作用。结果　成功建立了HIV21 慢性感染J urkat 细胞系(J urkat/ HIV21 ⅢB ) ,感染细胞阳性率> 90 %。检测影响病毒复制各周期的抗病毒药物对J urkat/ HIV21 ⅢB细胞的作用,发现J urkat/ HIV21 ⅢB细胞具有 HIV21 慢性感染细胞的生物学特征。结论　成功建立J urkat/ HIV21 ⅢB 细胞系,为抗HIV21 药物的研发和病毒感染机制研究提供了新的工具。

Bioactive Nortriterpenoids from Schisandra grandiflora

Three new nortriterpenoids, schigrandilactones A-C (1-3), along with eight known compounds, were isolated from an organic solvent extract of Schisandra grandiflora. Compounds I and 2 feature a spirocyclic moiety in their structures, and compound 3 was cha

Culture potential of Amblypharyngodon mola with carps in polyculture in farmers' pond of northern regions of Bangladesh

To assess the culture potential of mola (Amblypharyngodon mola) along with carps in polyculture systems, an experiment consisted of three treatments each with five replications was conducted for 4 months in two villages of Parbatipur upazilla under Dinajpur district. In the first treatment (SS), catla, rohu, mrigal, grass carp, Thai punti, common carp and a higher density of silver carp (8 per 40m²) were stocked. In the second treatment (SM), stocking density of silver carp was reduced to half and mola was added at a stocking density of 12,500/ha with all other fishes used in SS. In the third treatment (MM), no silver carp was stocked and mola was added at a stocking density of 25,000/ha with all other fishes used in SS. All treatments were subjected to the same regime of feed and fertilizers. The yields of large carps were 2035 kg/ha, 1757 kg/ha and 1326 kg/ha for treatments SS, SM and MM, respectively. Catla, grass carp and carpio showed better growth and production performance in presence of mola at a higher density, while rohu, Thai punti and mrigal showed better performance when stocking density of mola was relatively low. Mola yield was almost two times higher (184 kg/ha) in absence of silver carp (MM) than (62 kg/ha) in presence of silver carp (SM). The result showed that there was a significantly (p<0.01) lower total fish production in treatment MM. But there were no significant difference in total production between treatment SS and SM.

On the fishes and fisheries of Lake Baringo

Six fish species are known to occur in Lake Baringo. Tilapia nilotica Linnaeus 1757, Barbus gregorii Boulenger 1902, Clarias mossambicus Peters 1852 and Labeo cylindricus Peters 1852 were recorded in 1930-31. In 1969, two more fish species were identified: Aplocheilichthys sp. and Barbus lineomaculatus Boulenger 1903. T. nilotica is the only fish species commercially exploited. But the catches, catch per unit effort and the mean size of fish caught in commercial gillnets have declined since 1968. B. gregorii is important in the subsistence rod-and-line fishery. L. cylindricus, C. mossambicus, B. lineomaculatus and Aplochelichthys sp. are not commercially exploited.