关于岩芋属二个种的模式化问题

岩芋属Remusatia(Araceae)是一个特征鲜明的属,共含三种,即R. vivipara(Lodd. )Schott,R. hookeriana Schott,R. ornata(Schott)H. Li et Q.F.Guo。Gonatanthus (?) ornatus Schott中的 (?) 这类植物转入Remusatia属,其名应为秀丽岩芋Remusatia ornata(Schott)H. Liet Q. F. Guo. Gonatanthuc ornatus 的模式标本是Hooker f.s.n.采自印度喀西山,现只有Schott绘制的模式图照片;Schlagintweit n.313,亦采自喀西山,是Krause(1920)补充描述本种的重要凭证标本,现只有遗图。R. hookeriana Schott(1857)的模式标本Hooker f.s.n.产锡金,Krause(1920)发表的图和描述的大部分可作为该种的凭证,是一个不同于R. ornata的好种。Rao et Verma(1968)所描述的Gonatanthus ornatus应是Remusatia hookeriana。     

天南星科岩芋属的细胞地理学研究

本文报道了岩芋属三个种的染色体数目和核型:岩芋Remusatia vivipara是三倍体,核型公式为K(2n)=3X=42=42m;早花岩芋R. hookeriana为二倍体,核型公式为K(2n)=2X=28=22m(6SAT) 6m(2SAT);秀丽岩芋R. ornala,也是三倍体,核型公式为K(2n)=3X=42=36m(3SAT) 3sm 3st。在岩芋属中,岩芋是一个比较原始的种,秀丽岩芋较进化。岩芋属是热带非洲和热带亚洲间断分布的小属,它的原始类群岩芋(R. vivipara)的原始居群(二倍体居群)分布在印度南部,因而作者没想,古南大陆是岩芋属的起源地,本属向热带亚洲的扩散是与第三纪时喜马拉雅造山运动相联系的。     

假尾孢属三个未描述种

本文报道了寄生于喜树上的喜树假尾孢(Pseudocercospora camptoMecae Liu et Guo,sp(?)nov(?))、寄生于杜仲上的杜仲假尾孢(Ps.eucommiae Guo et Liu,sp.nov.)和寄生于堇菜属植物上的堇菜生假尾孢(Ps.violaecola Liu et Guo,sp.nov.)三个新种。模式标本保藏于HMAS,北京。     

窄腹细蜂属二新种(膜翅目:窄腹细蜂科)

报遭窄腹细蜂属Ropronia Provancher 2 新种：梵净山窄腹细蜂R．fanjingshanensis He et Chen．sp．nov．和双斑窄腹细蜂R．bimaculata He et Chen,sp．nov。均采自贵州省。描述了形态特征并与近似种做了比较。模式标本保存于杭州浙江大学植物保护系寄生蜂标本室。     

河北省有瓣蝇类研究(一)(双翅目:蝇科)

整理近年来采自河北省蝇科标本,发现阳蝇属Helina R.-D.二新种和棘蝇属Phaonia R.-D一新种,特此描述。模式标本存于沈阳师范学院生物系。 1.黑古阳蝇Helina nigricnnosa Xue et Zhao,新种(图1—4)     

中国腺水螨科一新纪录亚属拟腺水螨亚属及一新纪录种记述(水螨群,腺水螨总科,腺水螨科)

记述了采自中国腺水螨科1新纪录亚属,拟腺水螨亚属Pseudolebertia Thor,1897及1新纪录种,光足腺水螨Lebertia(Pseudolebertia)abseta Guo,Jin et Asadi,2006.检视标本存放于贵州大学昆虫研究所.     

尾孢菌属五个新种

本文报道尾孢菌属五个新种,即美人蕉尾孢(Cercospora cannae Bai,Liu et Guo,sp.nov.),败酱尾孢(C.patriniae Liu et Guo,sp.nov.),骆驼蓬尾孢(C.pegani Liu et Guo,sp.nov.),旌节花尾孢(C.stachyuricola Liu et Guo,sp.nov.)和安息香尾孢(C.styracicola Liuet Guo,sp.nov.)。文中对各个新种作了汉文描述和附图,并有拉丁文特征简介。模式标本收藏于中国科学院真菌标本室。     

Sauromatum gaoligongense(Araceae), a New Species from Gaoligong Mountains

本文描述了天南星科斑龙芋属一个新种,高黎贡山斑龙芋Sauromatum gaoligongense Z.L.Wang et H.Li,其显著特点是叶柄下部具3～5枚株芽。     

中国南海单肢水母属二新种(丝螅水母目,高手水母科)

记述了采自南海花水母亚纲Anthomedusae Haeckel,1879、丝螅水母目Filifera Kühn,1913、高手水母科Bougain villidae Lütken,1850、单肢水母属Nubiella Bouillon,19802新种,即球形单肢水母N. globosa Lin,Xu et Huang,sp.nov.和球腺单肢水母N. globogona Wang,Guo et Xue,sp.nov.,对新种特征进行了绘图和描述。模式标本保存于国家海洋局第三海洋研究所。     

中国新纪录属(半翅目,叶蝉科,片角叶蝉亚科)及二新种记述

记述片角叶蝉亚科中国1新纪录属,皱背叶蝉属Rhytidodus Fieber,1新纪录种,黄斑皱背叶蝉R.melanthes Anufriev,2新种:杨皱背叶蝉R.poplara Li et Yan,sp.nov.和扎兰屯皱背叶蝉R.zalantunensis Li et Zhang,sp.nov.。新种模式标本保存在贵州大学昆虫研究所。     

Chemical analysis of new water-soluble (1→6)-, (1→4)-α, β-glucan and water-insoluble (1→3)-, (1→4)-β-glucan (Calocyban) from alkaline extract of an edible mushroom, Calocybe indica (Dudh Chattu)

Two different glucans (PS-I, water-soluble; and PS-II, water-insoluble) were isolated from the alkaline extract of fruit bodies of an edible mushroom Calocybe indica. On the basis of acid hydrolysis, methylation analysis, periodate oxidation, and NMR analysis ((1)H, (13)C, DEPT-135, TOCSY, DQF-COSY, NOESY, ROESY, HMQC, and HMBC), the structure of the repeating unit of these polysaccharides were established as: PS-I: →6)-β-D-Glcp-(1→6)-β-D-glcp-(1→6)-)-β-D-Glcp-(1→ α-D=Glcp (Water-soluble glucan). PS-II: →3)-β-D-Glcp-(1→3)-β-D-glcp-(1→3)-)-β-D-Glcp-(1→3)-β-D-Glcp-(1→ β-D-Glcp (Water-insoluble glucan, Calocyban).     

西昆仑山区高等真菌的研究

本文报道了西昆仑山区和喀喇昆仑山区高等真菌39种,其中我国新纪录4种。     

Chemical Constituents of Glycyrrhiza eurycarpa P. C. Li (1I)

Huang Gancao (Glycyrrhiza eurycarpa P. C. Li) is a new species discovered recently. Its chemical constituents have not been reported before. This paper reports the isolation of ten components (Ⅰ—Ⅹ) from its roots and rhizomes collected in Jinta County, Gansu Province. On the basis of physico-chemlcal constants and spectroscopic (IR, UV, 1HNMR, 13CNMR, MS, and CD) analysis, they were identified as ononin(Ⅰ), liquiritigenin 4 -O-β-D-apio-D-franosyl-(1 →2)-β-D-glucopyranoside(II), isoliquiritigenin-4-O-β-D-apio-D-franosyl-(1→ 2) β-D-glucopyranoside (Ⅲ), choerospondin (Ⅳ), violanthin (Ⅴ), isoviolan thin (Ⅵ), vicenin-2(Ⅶ), uralsaponin A(Ⅷ), daucosterol (Ⅸ), and phloretic acid (Ⅹ), respectively All of them were isolated from this plant for the first time. Choerospondin, violanthin, daucosteroi and phloretic acid were not found in this genus before.     

被子植物系统发育研究的现状与展望

为植物界最大的类群—被子植物建立一个能真正反映植物的进化历史和系统发育（phylogeny）的分类系统一直是许多植物系统学家和进化学家所向往的。到目前为止,已经提出的被子植物分类系统至少有二十多个。问题在于这样的分类系统能否说已符合于系统发育的要求？要回答这个问题,首先必须弄清系统发育的真正含义是什么。     

Structures of verbascoside and orobanchoside,caffeic acid sugar esters from Orobanche rapum-genistae

The complete structural elucidation of the two caffeic acid sugar esters verbascoside and orobanchoside, has been realized by ¹H and ¹³C NMR studies. It has been demonstrated that verbascoside is β-(3′,4′-dihydroxyphenyl)ethyl-O-α-L-rhamnopyranosyl(1→3)-β-D-(4-O-caffeoyl)-glucopyranoside, and orobanchoside is β-hydroxy-β-(3′,4′-dihydroxyphenyl)-ethyl-O-α-L-rhamnopyranosyl(1→2)-β-D-(4-O-caffeoyl)-glucopyranoside.     

Passibiflorin,epipassibiflorin and passitrifasciatin: cyclopentenoid cyanogenic glycosides from Passiflora

An epimeric mixture of two novel cyclopentenoid cyanogenic glycosides, passibiflorin [1-(6-O-β-D-rhamnopyranosyl-β-D-glucopyranosyloxy)-4-hydroxycyclopent-2-en-1-nitrile] and its C-1 epimer, epipassibiflorin, has been isolated from Passiflora biflora and P. talamancensis. The structures were determined by means of ¹H NMR and ¹³C NMR. Another novel cyclopentenoid cyanogenic glycoside, passitrifasciatin [1-(4-O-β-D-rhamnopyranosyl-β-D-glucopyranosyloxy)-4-hydroxycyclopent-2-en-1-nitrile] is described from Passiflora trifasciata. The structure was determined by means of ¹H NMR. The identification of the sugar moieties was made by HPLC and TLC. The isolation of a β-1 → 4 and a β-1 → 6-rhamnoglucoside of cyclopentenoid cyanogens from three species of subgenus Plectostemma of Passiflora suggests that diglycosides of this type are taxonomically diagnostic for the section.     

Molluscicidal saponins from Gundelia tournefortii

From the roots of Gundelia tournefortii seven saponins have been isolated mainly by DCCC. The main saponins (A and B) were characterized, mainly by ¹³C and ¹H NMR spectroscopy, as oleanolic acid 3-O-(2-[α-l-arabinopyranosyl(1 → 3) -β-d-gentiotriosyl(1 → 6) -β-d-glucopyranosyl]gb-d-xylopyranoside) (saponin A) and oleanolic acid 3-O-(2-[α-l-arabinopyranosyl] (1 → 3)-β-d-gentiobiosyl (1 → 6)-β-d-glucopyranosyl β-d-xylopyranoside) (saponin B). The other saponins are also derived from oleanolic acid and contain more sugar units. The saponin mixture and the saponins A and B possess strong molluscicidal activity against the schistosomiasis transmitting snail Biomphalaria glabrata.     

Structural studies of the capsular polysaccharide produced by Leuconostoc mesenteroides ssp. cremoris PIA2

The structure of the capsular polysaccharide (CPS) produced by Leuconostoc mesenteroides ssp. cremoris PIA2 has been determined using component analysis and NMR spectroscopy. (1)H and (13)C resonances were assigned using 2D NMR experiments, and sequential information was obtained by (1)H,(1)H-NOESY and (1)H,(13)C-HMBC experiments. The CPS consists of linear pentasaccharide repeating units with the following structure: →3)-β-D-Galf-(1→6)-β-D-Galf-(1→2)-β-D-Galf-(1→6)-β-D-Galf-(1→3)-β-D-Galp-(1→, in which four out of the five sugar residues have the furanoid ring form, a structural entity found in bacteria but not in mammals. The analysis of the magnitude of the homonuclear three-bond coupling constants of the anomeric protons for the five-membered sugar rings indicates that the sugar residues substituted at a primary carbon atom show one kind of conformational preferences, whereas those substituted at a secondary carbon atom show another kind of conformational preferences.     

Study on Chemical Constituents of Gentianopsis barbata var. Stennocalyx H. W. Li ex T.N. Ho

Nine compounds were isolated from Gentianopsis barbata var. stennocalyx H. W. Li ex. T.N.Ho. Their structures are identified as 1-hydroxy4, 7, 8-trimethoxyxanthone (Ⅰ), 1, 7-dihydroxy-3, 8-dimethoxyxanthone (Ⅱ), 1, 7, 8-trihydroxy-3-methoxyxanthone (Ⅲ), 1-O-(β-D- xylopyranosyl-(1→6)-β-D-glucopyranosyl)-3, 7, 8-trimethoxyxanthone (Ⅳ), 1-O-(β-D-xylopy- ranosyl- (1→6)-β-D-glucopyranosyl)-7-hydroxy-3, 8-dimethoxyxanthone (Ⅴ), 1-O-(β-D-xylo- pyranosyl-(1→6)-β-D-glucopyranosyl)-7, 8-dihydroxy-3-methoxyxanthone (Ⅵ), luteolin-7-O- β-D-glucoside (Ⅶ), oleanolic acid (Ⅷ) and ursolic acid (Ⅸ) by means of chemical methods and UV, IR and NMR determinations respectively.     

Identification and Isolation of Steroidal Saponins of Dioscorea zingiberensis Wright

Two diosgenin trisaccharides (A,B) and two furostanolic tetrasacharides of diosgenin (C, D) had been isolated from Dioscorea zingiberensis wright. By means of acetylation, acid hydrolysis, enzymolysis, IR, MS, 1H-NMR and 13C-NMR, saponin A was proved to be a new compound of structure: diosgenin-3-O- [ β-D-glucopyranosyl (1 → 2) ]-O- [ α-L-rhamnopyra- nosyl (1→3)]-O-β-D-glucopyranoside was provisionally named zingiberenin A; saponin B may be suggested as the steric isomer of gracillin; saponin C was identified as 26-O-β-D- glucopyranoside of A and saponin D as 26-O-β-D-glucopyranoside of B. The last two components named proto-zingiberenin A and proto-zingiberenin B respectively.