Viruses' complete genomes classification based on geometrical learning

In this paper, we proposed a method of classification for viruses' complete genomes based on graph geometrical theory in order to viruses classification. Firstly, a model of triangular geometrical graph was put forward, and then constructed feature-space-samples-graphs for classes of viruses' complete genomes in feature space after feature extraction and normalization. Finally, we studied an algorithm for classification of viruses' complete genomes based on feature-space-samples-graphs. Compared with the BLAST algorithm, experiments prove its efficiency.

Surface plasmon coupling in hexagonal textured metallic microcavity

The coupling of surface plasmons to the photonic modes in hexagonal textured metallic microcavity was studied. The modified photonic modes enable efficient coupling with the luminescence source in the microcavity. Hexagonal photonic crystal lattice has higher folding symmetry providing more channels for surface plasmon coupling in different in-plane directions, i.e., more isotropic light extraction profile than one-or two-dimensional gratings. Results show that strong coupling between surface plasmon modes and the waveguide mode in the microcavity has led to angle-selective enhanced light extraction and it was as much as 12 times more light extracted compare to planar microcavity. (c) 2006 American Institute of Physics.

crossmodal error correction of continuous handwriting recognition by speech

In recognition-based user interface, users’ satisfaction is determined not only by recognition accuracy but also by effort to correct recognition errors. In this paper, we introduce a crossmodal error correction technique, which allows users to correct errors of Chinese handwriting recognition by speech. The focus of the paper is a multimodal fusion algorithm supporting the crossmodal error correction. By fusing handwriting and speech recognition, the algorithm can correct errors in both character extraction and recognition of handwriting. The experimental result indicates that the algorithm is effective and efficient. Moreover, the evaluation also shows the correction technique can help users to correct errors in handwriting recognition more efficiently than the other two error correction techniques.

基于文本比较的需求变更信息挖掘和分析方法

需求变更是需求工程中不可避免的问题，会持续发生并贯穿于整个软件开发的生命周期中，并且会对项目的成本、进度、质量等多方面造成影响。需求度量工作是一个开发组织成长和进步的必要手段，也是对项目经验进行学习和总结最佳途径。只有做好了需求变更度量工作，才能逐渐了解需求变更的规律，这对于改善需求管理的质量，提高需求的可信度，都有着重要的作用。需求变更过程会导致大量的需求文档的版本产生，但是这些变更信息往往没有得到很好的记录，这使得需求度量工作变得很困难。 一般来讲，由于使用了配置管理工具，大的需求版本变更一般都可以直接从配置管理工具得到。但是很多小的变更仅仅反映在文档上，没有纳入配置管理或者没有填写变更信息，并且很多公司都仅仅使用word文档进行需求管理。一个项目会产生大量这种word文档，而变更的信息往往得不到很好的记录，这部分信息丢失了。一个项目的需求会发生很多次或大或小的变更，产生文档版本的数量是非常多的，这部分文档的变更信息如果完全采用人工阅读获取，工作量是非常巨大的，实施起来非常不实际。 本文采用文本相似度比较的方法，对word文档中的变更信息进行还原。识别文档的中需求的相似程度，然后根据设定的阈值来恢复出需求变更的增、删、改等信息。并且本文设计和实现了需求文档变更信息挖掘工具，采用工具恢复变更信息的方法相对手工查看，解决了手工查看费时费力的缺点，并且由于需求文档演化的逻辑连续性，大部分比较都是在相邻的变更版本之间，文档变化幅度不会特别大，准确性也可以得到较好的保证。本文最后采用了实际的项目文档数据对方法进行验证，验证了方法的有效性和准确度。

原油在扰动土壤中入渗的实验研究

随着国家发展对能源的迫切需求,石油作为我国能源的主要构成之一,其开采和冶炼也在不断地增加。然而由于某些相关管理环节的不完善引发的污染事故日趋增多,其中原油的土壤污染问题尤为严重。为研究原油在土壤中的入渗过程,通过室内土柱模拟实验,测定了原油在土壤中入渗的湿润距离、湿润推进速率与时间的关系以及被原油污染的土壤中残留物的含量。结果表明:对于同一质地土壤,随着容重的增加,原油在土壤中入渗的湿润距离、湿润推进速率和残留物的含量均降低;容重相同而质地不同的土壤,随着粉粒含量的增加,原油在土壤中入渗的湿润距离、湿润推进速率和残留物的含量均表现为降低趋势;原油在土壤中入渗的湿润距离随时间的变化可以用对数函数拟合,湿润推进速率与时间的关系可以用幂函数拟合,均达到显著水平。研究原油在土壤中的入渗对于了解原油在土壤中的迁移有着重要的意义。

黄土高原沟壑区王东沟流域土地利用/覆被变化过程初探

黄土高原沟壑区王东沟流域从1986年至2006年的土地利用/覆被发生了较大变化,土地利用动态指数分别为:耕地3.21%,园地-36.11%,林地-4.05%,牧草地4.24%,居民点及独立工矿用地-0.62%,交通运输用地-12.27%,未利用地1.85%;变化趋势是:耕地逐年向园地流转,园地变化烈度较大,其他各类用地变化不太显著。引起这一变化的主要因素是自然、社会、经济、技术以及政策因素。结合这一变化,针对黄土高原沟壑区的实际情况,在黄土高原沟壑区土地利用经营与管理方面,应重视土地产出效益与粮食安全的关系,在保障区域粮食安全的基础上实现效益最大化。

离子液体在铈（IV）钍及稀土（III）萃取分离中的应用研究

本文对1-辛基-3-甲基咪唑六氟磷酸盐离子液体（[C8mim]PF6）在包头稀土矿分离钍以及攀西矿分离铈工艺中的应用作了初步探索。论文首先研究了伯胺N1923溶于离子液体对硫酸体系钍的萃取分离行为，考察了酸度、盐析剂浓度、萃取剂浓度等对N1923/IL萃取钍的影响，并与庚烷体系的萃取规律作了对比。在此基础上对萃取机理进行了探讨，提出了不同于分子溶剂体系的萃取机理，认为N1923/IL在水相有硫酸钠作为盐析剂时对钍的萃取为“胶束增溶”萃取机理。此外，钍对稀土的分离考察结果认为，虽然N1923/IL对钍的萃取效率降低，但在一定条件下钍对稀土仍能保持较高的分离系数。由此本文对N1923/IL应用于钍的分离实践作了初步评估。 论文的另外一部分工作研究了纯[C8mim]PF6及其与2-乙基己基膦酸二（2-乙基己基）酯（DEHEHP）的混合体系对硝酸铈（IV）的萃取性能。研究发现纯[C8mim]PF6本身对硝酸铈（IV）有良好的萃取选择性，机理考察结果认为铈（IV）的萃取是由于Ce4+离子在富硝酸根溶液中形成络阴离子Ce(NO3)62-并与离子液体的阴离子PF6—发生交换的结果。一种新型含铈离子液体[C8mim]2Ce(NO3)6的合成进一步证实了这一机理。反萃考察发现被萃入离子液相的铈（IV）用水可完全反萃，且萃取和反萃过程中因离子交换机理导致的离子液体流失可以通过添加适量离子液体组分的方法予以抑制。此外，本文考察了DEHEHP溶于[C8mim]PF6对于含氟硝酸体系铈（IV）的萃取行为，发现在一定条件下DEHEHP对铈（IV）的萃取能获得与分子溶剂中等同的萃取机理。在此基础上，采用DEHEHP/IL从氟碳铈矿分解液中进行分离铈和氟的研究，获得纯度为99.9%以上的纳米CeF3产品。由此我们提出一个将离子液体应用于攀西氟碳铈矿铈钍稀土分离流程的模型，为离子液体在稀土清洁分离流程中实现溶剂绿色化的目标提供了一个范例。

稀土元素与过渡金属元素的溶剂萃取与树脂吸附研究

该论文围绕金属元素的溶剂萃取和树脂吸附进行了一系列研究.考察了几种萃取剂的混合体系对稀土元素及过渡金属元素的萃取效应,同时,研究了酸性有机磷(瞬)类萃淋树脂对二价过渡金属元素的吸附性能,并讨论了它们用于分离金属元素的可能性.1.研究了盐酸和硝酸介质中β-二酮类萃取剂HPMBP与硫代中性有机磷(膦)类萃取剂Cyanex471X单独及混合体系对稀土元素La(Ⅲ)的萃取机理.2.研究了Cyanex272与伯胺N1923的混合物对Zn(Ⅱ)的协同萃取效应,得出了协萃反应方程式和平衡常数.3.考察了伯胺N1923与中性有机磷(膦)类萃取剂DEH/EHP的混合体系在盐酸介质中对Zn(Ⅱ)和Cd(Ⅱ)的萃取效应,研究了萃取机理,并研究了此混合体系对Zn(Ⅱ)和Cd(Ⅱ)的分离.4.揭示了Cyanex923萃取硝酸过程中出现第三相的机理和三相的相行为,讨论了第三相形成的影响因素.5.考察了盐酸介质中HEOPPA萃淋树脂对二价过渡金属元素的吸附平衡,得出了吸附反应方程式.

阿片类药物成瘾者瞳孔光反射的检测和特征提取

建立了一种基于图像处理的快速瞳孔直径检测算法,运用此算法提取了反映阿片类药物成瘾人员与正常人对瞳孔光反射变化差异的3个特征值:绝对收缩幅度(absolute amplitude of contraction,AAC)、相对收缩幅度(relative amplitude of contraction,RAC)和收缩斜率(SCV,slope of contraction velocity);分别研究了成瘾、性别、近视、年龄、睡眠剥夺等因素对于这3个特征值的影响。不同性别、近视人员、睡眠剥夺人员与正常人之间的3个特征值均无显著差异,成瘾人员与之对比均显著减小。老年人相对于正常青年人,3个特征值都明显减小;与成瘾人员相比,仅在RAC值上有显著差异。结果表明,阿片类药物成瘾人员除了与正常人外,也与其他具有潜在影响瞳孔变化因素的非阿片成瘾人员在瞳孔对光反射的特征值上具有显著差异。该研究的实验数据为进一步建立基于检测瞳孔对光反射其直径发生变化的方法来快速、非接触地鉴别出阿片类药物成瘾人员提供了可靠的依据。

矿山废弃物中重金属污染行为及其对白菜品质的影响

综合运用环境地球化学、土壤学、生态学和统计学的方法开展了矿山废弃物尾矿石的堆置对土壤造成的污染以及矿区土壤重金属污染对白菜（Brassica Chinensis）的卫生品质和营养品质的影响研究。静态培养试验和动力学淋溶试验证明：在环境因素（如降水）的作用下，尾矿石的堆置将对下伏土壤的重金属含量产生长久影响，随着降水量以及酸度的增加，土壤中Cu、Cd、Pb、Zn的全量和有效态含量都有所升高并且土层间的差异减小。有机酸能不同程度地促进土壤中的重金属转化为有效态，增强重金属的生物有效性；多元梭酸比一元梭酸的转化率高。另外，有机酸对重金属的转化作用随其浓度的增大而增强，在低温范围内，随温度的升高而增加。通过网室盆栽试验，研究了土壤受Cu、Cd、Pb，Zn单一重金属污染后对大白菜吸收Cu、Cd、Pb、Zn以及植物体内粗纤维和维生素C含量的影响；同时还进一步对Cd-P交互作用影响大白菜吸收Cd、P以及植物体内粗纤维和维生素C含量的情况进行了研究，结果表明大白菜从污染的土壤吸收重金属与土壤中目标元素的含量呈极显著正相关，对非目标重金属的吸收情况复杂，因不同元素间的相互作用机制而异；白菜体内粗纤维和抗坏血酸含量随土壤重金属浓度的增加而降低，它们之间呈极显著的负相关关系。在采用大白菜进行高等植物毒性试验的基础上，首次运用典型相关分析方法对Cu、Cd、Pb、Zn复合污染土壤的生态毒性进行了评价，分别建立了由4元素共同组成的复合污染土壤毒性的线性组合函数和由芽生物量抑制率和根伸长抑制率组成的植物学表征的线性组合函数，并计算了其第一典型变量Toxl（土壤毒性）和BloL（植物学表征）之间的相关系数为0.94（p＜0.01）。典型相关分析是介质毒性评价的有效方法之一。

双花千里光、川芎及宽叶羌活的化学成分研究

本论文由四章组成。第一、二和三章分别报道了双花千里光、川芎和宽叶羌活的化学成分研究。从三种药用植物中共分离和鉴定了40 个化学成分，其中8个为新化合物。第四章概述了藳本属植物及日本川芎的化学成分研究进展。 第一章包括三个部分。第一部分报道双花千里光（Senecio dianthus Franch.）地上部分乙醇提取物的化学成分。采用正、反相硅胶柱层析等各种分离方法，从中共分离出8 个艾里莫酚型倍半萜内酯，其中5 个是新化合物，并且有1 个为首次发现的连接了含氮原子取代基的艾里莫酚型倍半萜内酯。它们的结构经MS、IR、NMR及X-单晶衍射等解析方法确定为2b-angeloyloxy-10b-hydroxyeremophil-7(11)-en-8a,12-olide (1)、6b-angeloyloxy-10b-hydroxyeremophil-7(11)-en-8a,12-olide (2)、2b-angeloyloxy-8b,10b- dihydroxyeremophil-7(11)-en-8a,12-olide (3)、2b-angeloyloxy-8a-hydroxyeremophil-7(11),9(10)-dien-8b,12-olide (4)和8b-amino-10b- hydroxyleremophil-7(11)-en-8a,12-olide (5)。这8 个倍半萜内酯经体外生物活性测试表明均具有通过抑制巨噬细胞增殖抵制破骨细胞增生的活性。第二部分对艾里莫酚型倍半萜内酯的质谱裂解规律进行了初步探讨。第三部分报道双花千里光茎、和叶花的挥发油成分分析。采用传统水蒸气蒸馏法分别提取了双花千里光茎、叶和花的挥发油，用气相色谱－质谱联用（GC-MS）技术分别分离鉴定了其化学成分，从茎、叶和花挥发油中各分离和鉴定出70、80 和73 种化学成分，分别占挥发油总量的91.2％、85.7％及93.4％。 第二章包括两个部分。第一部分报道川芎（Ligusticum chuanxiong Hort.）根茎乙醇提取物的化学成分。通过正、反相硅胶柱层析等分离纯化和MS、NMR及X-单晶衍射等解析方法，共分离鉴定了21 个化合物，结构类型分属于苯酞、二聚苯酞、香豆素和脂肪酸类。其中2 个为结构比较新颖的二聚苯酞类化合物：chuanxiongnolide A (19)和chuanxiongnolide B (20)，化合物19 的结构经X-单晶衍射得到确证。第二部分报道川芎挥发油的化学成分。采用不同的提取方法（溶剂萃取法、水蒸气蒸馏法、CO2 超临界流体萃取法）提取川芎挥发油，同时采集不同产地（四川彭县、四川郫县、云南鹤庆）及不同品质（川芎、奶芎、苓子）的川芎产品，利用GC-MS 技术分离鉴定其挥发油的化学成分，计算各成分的相对含量，并对比分析其中的异同。 第三章报道宽叶羌活（Notopterygium forbesii Boiss.）根茎化学成分的分离纯化和结构鉴定。通过正、反相硅胶柱层析等分离纯化和MS、NMR 等解析方法，共分离鉴定了13 个化合物，结构类型分属于香豆素、二氢异香豆素、甾体和羧酸类。其中1 个新二氢异香豆素类成分鉴定为6-methoxy-hydrangenol (37)。 第四章概述了藳本属植物及日本川芎化学成分的研究进展。 This dissertation consisted of four chapters. The former three chaptersrespectively elaborated the phytochemical investigation of three herbal medicines:Senecio dianthus Franch., Ligusticum chuanxiong Hort. and Notopterygium forbesiiBoiss.. Forty compounds, including eight new ones, were isolated and identified byspectral and chemical evidence. The fourth chapter elaborated the study progress ofchemical constituents of Ligusticum genus and Cnidium offcinale. The first chapter consisted of three parts. The first part is about the chemicalconstituents of ethanol extraction and essential oils from the aerial parts of S. dianthu.Eight eremophilenolides were isolated and identified. Among them, five ones are newcompounds and one of them is a novel eremophilenolide attched with an amino group.The structures of the new compounds were identified as 2b-angeloyloxy-10b-hydroxyeremophil-7(11)-en-8a,12-olide (1)，6b-angeloyloxy-10b-hydroxyeremophil-7(11)-en-8a,12-olide (2)，2b-angeloyloxy-8b,10b-dihydroxyeremophil-7(11)-en-8a,12-olide (3)，2b-angeloyloxy-8a-hydroxyeremophil-7(11),9(10)-dien-8b,12-olide (4) and8b-amino-10b-hydroxyeremophil-7(11)-en-8a,12-olide (5) by spectral evidence andX-ray crystallography analysis. All the compounds were evaluated for theiranti-osteoclstogenesis activity using a proliferation inhibit assay with microphagecells. The second part elementarily discussed the characteristic fragmentation oferemophilenolides isolated from S. dianthus in ESI-MS.The latter part is about thechemical constituents of essential oil extracted from stems, leaves and flowers of S.dianthus with steam distillation. By the GC-MS analysis, 70, 80 and 73 compoundswere respectively isolated and identified which accounted for more than 91.2％, 85.7％ and 93.4％ of total essential oil. The second chapter, including two parts, is about the the chemical constituents ofethanol extraction and essential oils from rhizomes of L. chuanxion. In the first part, twenty-one compounds were isolated and iedntified. Two ones are novel dimericphthalides and the structures were suggested as chuanxiongnolide A (19) andchuanxiongnolide B (20) by spectral evidence and confirmed by X-raycrystallography analysis. In the second part, the samples were collected from differentextract techniques (solvent extraction, steam distillation and supercriticalfluid extraction), different habitats (Peng and Pi counties, Sichuan province; Heqing,Yunnan province) and different qualities (Chuanxiong, Naixiong and Lingzi). Thechemical constituents of essential oil from L. chuanxiong were analyzed by GC-MS and were compared each other. The third chapter is about the chemical constituents of rhizomas of N. forbesii,which belongs to a endemic genus of China. Thirteen compounds were isolated andidentified. One of them is a new dihydroisocoumarin and the structure was identifiedas 6-methoxy-hydrangenol (37) by spectral evidence. The fourth chapter is a review on study progress of chemical constituents ofLigusticum species and Cnidium offcinale.

两种银莲花属植物的化学成分研究

本学位论文由5 章组成。第1 章报道了两头尖中三萜皂苷类化合物的全扫描电喷雾多级质谱分析及银莲花素A 的电喷雾质谱裂解规律；第2 和3 章报道了两种银莲花属药用植物化学成分的研究结果；第4 章报道了银莲花素A 的化学结构修饰及其对一种蛋白酪氨酸磷酸酯酶（PTP-1B）的抑制活性；第5 章综述了电喷雾质谱在皂苷类化合物结构鉴定中的应用进展。 第1 章报道了运用全扫描电喷雾多级质谱对两头尖中三萜皂苷类化合物的快速定性检测，共检测出18 个准分子离子峰，根据多级质谱数据并结合文献报道，对其中的15 个准分子离子峰进行了归属，并区分了一些同分异构体；更有意思的是，发现了3 个未见文献报道的三萜皂苷类化合物。根据它们的多级质谱数据，对其结构分别进行了初步解析。本章同时对银莲花素A 特殊的质谱裂解途径通过衍生物制备及其质谱分析进行了确认。 第2 和3 章，分别报道了两头尖和打破碗花花中水溶性多糖苷的分离纯化和结构鉴定。采用D101 大孔树脂和反复硅胶柱层析等分离手段，从两头尖水溶性部分分离得到8 个三萜皂苷类化合物，通过红外、电喷雾质谱和核磁共振等现代谱学方法，并结合传统的化学手段鉴定了它们的结构，其中4 个化合物为新化合物，分别命名为多被银莲花皂苷19、多被银莲花皂苷20、多被银莲花皂苷21和多被银莲花皂苷22。从打破碗花花水溶性部位分离得到6 个三萜皂苷类化合物，通过现代谱学手段，并结合传统的化学方法对它们进行了鉴定，其中1 个为新化合物，命名为打破碗花花苷H。 第4 章报道了以银莲花素A 及其同系物为先导化合物，进行化学结构修饰并对修饰产物进行广泛的生物活性筛选，发现在银莲花素A 及其同系物的结构中引入一些酸性基团后，其生物活性发生了变化，一些修饰产物显示出很强的PTP-1B 抑制作用，提示这些化合物有可能用于治疗II 型糖尿病。 第5 章综述了电喷雾多级质谱用于皂苷类化合物结构鉴定的研究进展。 This dissertation composes of five chapters. The first chapter elaborates the detection and qualification of the triterpenoidal saponins in Anemone raddeana by positive and negative full scan ESI-MSn. This part also reports the special fragmentation pathway of Raddeanin A by ESI-MS/MS. The second and third chapters present the phytochemical investigation of two medicinal plants from Anemone. The fourth part dwells on the structure modification of Raddeanin A and their inhibitory activity against PTP-1B. The last part is a review on the progress in the application of ESI-MSn in the structure identification of saponins. The first chapter reports the application of full scan ESI-MSn for fast analysis of triterpenoid saponins in Anemone raddeana. Eighteen quasi- molecular ion peaks were detected in the positive full scan ESI-MS and fifteen of them were identified by analysis of their tandem mass spectral data in the negative ion mode. Several isomers were differentiated. More interesting, three unreported triterpenoid saponins in this medicinal plant were detected and their structures were deduced according to the dissociation pathway of the known triterpenoidal saponins. This chapter also confirms the special fragmentation pathway of Raddeanin A by its derivative and the mass spectral analysis. The second and third chapters expatiate on the isolation and identification of the chemical constituents from A. raddeana and A. hupehensis. Eight compounds were isolated from the roots and stems of A. raddeana by methanol extraction and repeated column chromatography (including D101 and silica gel), and their structures were determined on the basis of IR, ESI-MS, NMR and chemical methods (including acid hydrolysis and alkaline saponification). Among them, four are new triterpenoid saponins and named as Raddeanoside R19, Raddeanoside R20, Raddeanoside R21 and Raddeanoside R22. Six compounds were isolated from the whole plants of A. hupehensis by the same methods as above, and their structures were also determined with the same way. One of them was confirmed to be new triterpenoid saponins and named as hupehensis saponin H. In the fourth chapter, in order to look for new active compounds, the structure of Raddeanin A and its analogs were modified. It was found that the modified products exhibited obvious inhibitory activity against PTP-1B when several acid groups were introduced. The fifth chapter summarizes the progress on the application of ESI-MSn in the structure identification of saponins.

厚朴中α-葡萄糖苷酶抑制活性成分研究

本论文由三章组成。 第一章是关于厚朴中具有α-葡萄糖苷酶抑制活性成分的研究。凹叶厚朴的乙醇提取物显示了较强的α-葡萄糖苷酶抑制活性。为了确定其活性成分，在活性测试的指导下，通过溶剂萃取、树脂吸附和反复硅胶柱层析等分离方法从凹叶厚朴乙醇提取物中分离得到6 个生物碱，并用质谱和核磁共振等波谱方法分别鉴定为：木兰箭毒碱，木兰花碱，鹅掌楸碱，蕃荔枝碱，罗默碱和Lysicamine。应用小肠α-葡萄糖苷酶模型测定了它们对α-葡萄糖苷酶的抑制作用。其中，番荔枝碱和木兰箭毒碱对α-葡萄糖苷酶相对抑制活性最好，分别为60%和62%；其它四个生物碱成分对α-葡萄糖苷酶的抑制活性几乎相当，鹅掌楸碱为46%，罗默碱为51%，Lysicamine 为49%，木兰花碱为51%。 第二章报道了厚朴酚的衍生物及其对α-葡萄糖苷酶的抑制活性。根据糖苷酶抑制剂的结构特点，设计合成了一系列厚朴酚的衍生物。厚朴酚经过Mannich 反应和环氧化及开环反应制备了一系列衍生物，经活性测试发现衍生物活性与取代基关系较大，其中5,5′-diallyl-3-((bis(2-hydroxyethyl)amino)methyl)biphenyl-2,2′-diol 的抑制活性最高，为72%。 第三章综述了厚朴的化学成分及药理活性两个方面的研究进展。 The dissertation consists of three chapters. The first chapter is about the study on the constituents with α-glycosidase inhibitory activity from Magnolia officinalis. The EtOH extracts of M. officinalis Rehd. et Wils showed good inhibitory activity against α-Glucosidase. In order to determine the active compounds, bio-assay was used to guide the isolation. Six known alkaloids were isolated by solvent extraction and repeated silica gel column chromatography, and their structures were identified as liriodenine, anonaine, roemerine, lysicamine, magnoflorine and magnocurarine by spectroscopic methods. The inhibitory activity against α-Glucosidase of these alkaloids was measured with alvine screening model of α-glucosidase. Among them, lysicamine and liriodenine have the best inhibitory activity at 60% and 62%, respectively. The other four alkaloids have close inhibitory activity, from 46% to 51%. The second chapter is about the derivation of magnolol and the inhibitory a ctivity of the derivatives. Seven derivatives of magnolol were prepared by Manni-ch reaction, epoxidation followed by ring-opening reaction. Biological activity as say indicated the inhibitory activity was related to substituting groups. Among them, 5,5′-diallyl-3-((bis(2-hydroxyethyl)amino)methyl)biphenyl-2,2′-diol had the highest activity at 72%. The third chapter is a review on the progress of M. officinalis including chemical constituents and pharmacological activity.

Effects of magnetic configuration on hot electrons in highly charged ECR plasma

To investigate the hot electrons in highly charged electron cyclotron resonance (ECR) plasma, Bremsstrahlung radiations were measured on two ECR ion sources at the Institute of Modern Physics. Used as a comparative index of the mean energy of the hot electrons, a spectral temperature, Tspe, is derived through a linear fitting of the spectra in a semi-logarithmic representation. The influences of the external source parameters, especially the magnetic configuration, on the hot electrons are studied systematically. This study has experimentally demonstrated the importance of high microwave frequency and high magnetic field in the electron resonance heating to produce a high density of hot electrons, which is consistent with the empirical ECR scaling laws. The experimental results have again shown that a good compromise is needed between the ion extraction and the plasma confinement for an efficient production of highly charged ion beams. In addition, this investigation has shown that the correlation between the mean energy of the hot electrons and the magnetic field gradient at the ECR is well in agreement with the theoretical models.中文摘要：ECR(电子回旋共振)离子源是产生稳定的强流多电荷态离子束流最有效装置。全永磁 ECR 离子源因其独特的特点为很多中小型多电荷态离子束流实验平台与离子注入机等系统所采用，为后者产生重复性好、稳定性强的多电荷态离子束流。本文着重论述了中国科学院近代物理研究所研制的几台全永磁多电荷态ECR离子源及其特性与典型性能，如能产生强流高电荷态离子束流的高性能全永磁离子源LAPECR2，能产生强流中低电荷态离子束流的LAPECR1，能产生多电荷态重金属离子束流的LAPECR1-M等。这些性能稳定的离子源为提高近代物理研究所相关试验平台的性能提供了关键的束流品质保障。