兰花蕉属植物染色体新计数

首次报道了国产兰花蕉属植物2种1变种的体细胞染色体计数,其中兰花蕉及其变种长萼兰花蕉为2n=54,为六倍体;海南兰花蕉为2n=18,为二倍体。分析了世界范围内兰花蕉属植物染色体数及其倍性的地理学关系。     

A new pollination system: dung-beetle pollination discovered in Orchidantha inouei (Lowiaceae, Zingiberales) in Sarawak, Malaysia

Lowiaceae, a family of the Zingiberales, comprise 11 species in the single genus Orchidantha. Here we present the first report on the pollination of Lowiaceae and describe a new system of dung-beetle pollination from Sarawak, Borneo. Orchidantha inouei has a zygomorphic flower located just above the ground. Observations revealed that the plant is visited frequently and is pollinated by scarabaeid dung beetles, mainly members of the genus Onthophagus. All four species of Onthophagus collected on O. inouei have also been caught using traps baited with dung or carrion in Borneo. Onthophagus was presumably attracted to the dung-like odor of the flower. Pollination of O. inouei is different from other examples of beetle pollination in that its flower provides neither reward nor protected space. Dung beetles are excellent at following a particular dung scent. Orchidantha is the only genus that includes species lacking floral nectar. It is interesting that this deception pollination using dung beetles was found in Zingiberales, in which all known species have mutual and specialized relationships with their long-distance, but costly, pollinators-bees, birds, and bats.     

Orchidantha crassinervia sp. nov. (Lowiaceae) from Guangxi,China

Here we describe and illustrate a new species, Orchidantha crassinervia sp. nov. (Lowiaceae), from Guangxi Province, China. The species is closely related to O. yunnanensis and O. virosa, but can be distinguished from these species in possessing a very thick midrib of the labellum, fewer flowers per inflorescence and by a shorter plant height. The species is known only from the three populations within 3 km.     

Orchidantha foetida (Lowiaceae) a new species from Thailand

Orchidantha foetida sp. nov. from NE Thailand is described and illustrated and a key to the three species occurring in Thailand is presented.     

濒危植物兰花蕉的核型研究

研究了濒危植物兰花蕉及其变种长萼兰花蕉的核型。结果表明,兰花蕉中期染色体的相对长度为5.00～7.78μm,核型公式为2n=6x=54=23m+3sm(1sec)+1st(sec);而长萼兰花蕉中期染色体相对长度为5.00～7.92μm,核型公式为2n=6x=54=22m+4sm(2sec)+1st(sec)。按Stebbins的分类,两者均属2A型。根据核形态的有关数据分析,进一步支持将长萼兰花蕉作为兰花蕉变种处理的观点。     

中国兰花蕉科植物花粉形态

使用扫描电镜及光学显微镜观察了国产兰花蕉科2种植物（兰花蕉及长萼兰花蕉）的花粉形态。它们的花粉粒呈豆形、两侧对称、异极、无萌发孔,中间部分的表面具稠密的条状雕纹,两端的为皱波状雕纹。两种花粉的雕纹有些区别。兰花蕉科花粉形态特征特别,不同于姜国其他7科的花粉,属特殊的花粉类型。     

A new species of Orchidantha (Lowiaceae) from Borneo

Orchidantha holttumii , a new species of Lowiaceae is described from Brunei. The chromosome number is 2n = 18     

Orchidantha inouei (Lowiaceae), a new species from Borneo

A new species, Orchidantha inouei , is described from Sarawak. Two types of paracladium in the inflorescence are reported with a discussion on the inflorescence morphology of Lowiaceae.     

长萼兰花蕉(Orchidantha chinensis var.longisepala)气味腺结构探究

兰花蕉科(Lowiaceae)植物开花时,位于唇瓣的特殊腺体结构——气味腺(osmophores)能够产生和释放类似粪便的腐臭气味吸引传粉者。本研究以该科植物长萼兰花蕉(Orchidantha chinensis var.longisepala)为材料,采用中性红染色法初步确定气味腺的位置,然后用扫描电镜观察气味腺表皮细胞形态、透射电镜观察分泌细胞的超微结构。结果显示,散发腐臭气味的气味腺位于长萼兰花蕉唇瓣上端近轴面;气味腺由多样性的表皮细胞及表皮下1~2层分泌细胞构成,腺体细胞具有细胞核大、细胞质浓、线粒体和内质网丰富等特点;长萼兰花蕉花气味的释放主要依靠角质小泡的破裂完成,推测挥发性的小分子有助于花气味的释放。本研究结果有助于揭示兰花蕉科植物与传粉者之间的互作关系,了解植物的传粉过程。     

长萼兰花蕉(Orchidantha chinensis var.longisepala)的繁育系统研究

通过野外观察并采用杂交指数（OCI）测定、花粉/胚珠比（P/O）检测、人工控制授粉等方法,对长萼兰花蕉（Orchidantha chinensis var.longisepala（D.Fang） T.L.Wu）种群的繁育系统进行了研究,采用常规石蜡切片与扫描电子显微镜（SEM）观察了柱头与"V"形黏盘的结构与形态。结果表明,长萼兰花蕉单花花期一般为18 d,依其花部形态的变化可分为蕾期、花萼未反转期、花萼反转期、唇瓣枯萎期、花萼枯萎期5个时期;根据杂交指数值为4、P/O值为253.89 ±21.09、人工异花授粉结实率分别为45%（2014年）和75%（2015年）,显示出长萼兰花蕉的繁育系统属于异交,且需要传粉者。石蜡切片观察到长萼兰花蕉黏盘区与柱头可授区之间是光滑的表皮细胞,结合人工授粉实验与分泌物含糖量测定结果表明,长萼兰花蕉的"V"形黏盘不具有可授性,其作用可能是分泌黏液附着在传粉者背部使其便于携带花粉。长萼兰花蕉整个花期环境湿冷、多雨且开花同步性较低,这些因素很可能造成其有效传粉媒介缺乏,影响了传粉成功;另一方面,长萼兰花蕉有性繁殖受到限制,其主要通过根状茎进行无性繁殖后代,所以分布范围比较狭窄。     

兰花蕉花的形态解剖学

兰花蕉（Orchidantha chinensis)的子房室顶部闭合后向上延长成延长部,实心,但有花柱沟和隔膜蜜腺管通过,隔膜蜜腺管,可分为中央蜜腺管和三条侧蜜腺管;中央蜜腺管位于三个心皮连接处,自子房室区下部产生,向上于延长部的部顶端终止;三条侧管分别位于两个心皮连接处,于子房室区近中部产生,开口于花柱基部。兰花蕉子房室区与延长部均具6枚雄蕊的维管束系统,即3枚心皮背束的伴束与3枚隔膜束,近轴面1枚事膜向上进入唇瓣的维管束系统,位于唇瓣的中央,致使兰花蕉仅具5枚功能雄蕊,唇瓣具双重结构,本文还讨论了兰花蕉科的系统发育位置。     

兰花蕉花部维管束系统的解剖学研究

兰花蕉花梗的维管束分散排列．子房基部的维管束排成两部分,外方为一轮大维管束环,中央为分散排列的小维管束区。前者的纸管束进入子房壁,后者进入子房的中轴,形成股座纸管束;及至延长都以后,股座维管束逐渐消失．子房壁上的维管束较易识别的有心皮背束、心皮背束伴束和隔膜束．三束心皮背束经延长部最终进入花柱和柱头．心皮背束指心皮背束务与其紧靠的大维管束,三枚心皮背束伴束最终分别进入三枚外轮雄蓝．三枚隔膜束中远轴面的两枚分别进入两校内轮雄蕊,而近轴面的一枚伴随着第六枚雄蓝的缺失最后进入唇瓣中央．子房壁其余的维管束进入延长部后,先向外分出一轮纸管束进入花幕,余下的中央部分排成一轮心形的线管来环．该环远轴面的维管束分为两半分别进入两枚侧生花瓣;近轴面即心形凹陷一侧初为两轮即外轮大的维管束与内轮小的维管束,后排成一轮并与近轴面的隔膜束一同进入唇瓣．兰花蕉的唇瓣既为花瓣成员,又含一枚缺失的雄蓝维管束,与姜目已报道的只来自退化雄蕊的竹芋科的兜状结构和美人蕉科、姜科、闭鞘姜科的唇瓣有明显区别．在旅人蕉科尚未有研究资料的情况下,作者根据已有资料,对姜目雄蕊维管束系统来源和结构进行比较,初步认为在姜目的系统演化上,兰花蕉科与芭蕉料更近．     

姜目芭蕉群植物种子解剖学研究及其系统学意义

研究了姜目芭蕉群代表植物象腿蕉属象腿蕉(Ensete glaucum)、旅人蕉属旅人蕉(Ravenala madagascariensis)与蝎尾蕉属Heliconia faranmansis?D6肿咏馄侍卣鳌＝峁砻鳎笸冉段藜僦制ぃ制し只霰砥ぁ⒑癖谧橹赴褪赴悖赴瞿谇邢虮谟刖断虮谠龊瘢缓系闱哂泻系闶矣牒系愣眩谥制ち恢榭浊兄榭琢旌涂赘堑姆只榭琢煳涡停赘侵挥赡谥制は赴钩桑褐榭浊制ぱ由煨纬芍制昵唬和馀呷?层细胞：内胚乳细胞径向延长,细胞内充满淀粉粒。旅人蕉具假种皮,种皮分化出外种皮、中种皮和内种皮,外种皮细胞纵向延长,中种皮为7-9层切向延长的薄壁细胞,内种皮为石细胞型：合点区无合点室,内种皮在此出现缺口,缺口为整体轮廓呈喇叭形的近等径薄壁细胞群填充;珠孔区无珠孔领与孔盖的分化：外胚乳缺,内胚乳发达。蝎尾蕉属的Heliconia faranmansis?D6肿游藜僦制ぃ制の薹只墒闾寤闲∏揖断蜓映げ⑴帕形だ缸吹谋”谙赴钩桑褐榭锥酥制は蛲庋由欤纬衫嗨平浦肿拥闹指纷唇峁梗何蘅赘怯胫榭琢斓哂杏晒ば纬傻挠不牵缓系闱肼萌私断嗨疲煌馀呷樵?-4层细胞,细胞壁波浪形弯曲,内胚乳发达。综合作者对兰花蕉(Orchidanha chinensis)和前人对芭蕉群的种子解剖学研究结果,初步总结了芭蕉群种子解剖学特征及其进化式样,讨论了姜目芭蕉群四科种子解剖学特征的系统分类学意义。     

兰花蕉种子的解剖学和组织化学研究

兰花蕉种子球形或近球形,具表皮毛,种脊不明显。种子包括假种皮、种皮、外胚乳、内胚乳和胚五部分。假种皮具３～４条粗毛状裂片,包围种子或不定向伸展;裂片最外方为１层表皮细胞和１～３层厚壁细胞,内方为薄壁细胞;表皮细胞和厚壁细胞的壁增厚并木质化;成熟时裂片下部１／２段中空。种皮由外珠被发育而来,但内珠被在种子发育后期才萎缩。种皮分化为外种皮,中种皮与内种皮;外种皮由１层表皮细胞构成,其细胞壁增厚并木质化;中种皮外方为２～３层厚壁细胞,内方由１２～１５层薄壁细胞构成;内种皮由１层径向延长的石细胞构成,其细胞壁网状增厚,胞腔不明显。外胚乳极不显眼,大部分只由１层切向延长的长方形细胞构成,局部为２～１７层细胞;外胚乳细胞主要含许多脂类物质及少量蛋白质颗粒,不含淀粉。内胚乳占据种子很大的体积,由通常径向延长的长方形、长条形或方形薄壁细胞构成;细胞内充满淀粉粒和通常一颗亦有２至多颗菱形或方形蛋白质晶体,脂类物质极少。胚圆柱形,胚根和胚芽不明显。种子珠孔区不分化出珠孔领和孔盖,但具柄,柄的远轴端边缘大部分着生假种皮,着生假种皮一侧柄略膨大。合点区内种皮出现极宽的缺口,缺口间为整体呈弧状长条形的合点区厚壁细胞群。较粗的种脊维管?     

世界柽麦蛾属支序生物地理学研究（鳞翅目： 麦蛾科）

基于对世界柽麦蛾属昆虫外部形态和外生殖器的形态学研究,选择了66个性状演变系列,通过PAUP*4b10软件对柽麦蛾属51种昆虫进行了支序系统学分析。分析结果认为heluanensis种团并不是一个单系群,柽麦蛾属被重新作了7个种团的划分。在支序系统学分析的基础上,柽麦蛾属昆虫的14个地理分布区域等级关系被重建,显示出古地中海地区复杂的历史,同时说明在该属分布格局中扩散事件客观存在。     

Intergeneric antigenic relation of Hafnia and Shigella (S. flexneri and S. boydii) bacteria

The O-antigenic relationships between Hafnia and Shigellae (S. flexneri and S. boydii) have been studied. For the first time the presence of antigenic relationship between Hafnia O19, O4, O9, O33, O5, O16, O12, O7, O29, O28, O10, O32, O24, O25, O18, O1, O13, O3, O22, O30, O37, O14, O11, O25, O23, O21, O28, O16, O24, O8, O26, O27 and S. flexneri la, lb, 2a, 2b, 4a, 4b, 6, 5a, 5b, as well as between Hafnia O10, O21, O35, O36, O9, O28, O8, O30 and S. boydii 1, 3, 6, 14, 2, 5, 2, 12 have been revealed. The character and degree of manifestation of antigenic relationships between the above-mentioned groups of bacteria have been established.     

Development of Three Multiplex PCR Assays Targeting the 21 Most Clinically Relevant Serogroups Associated with Shiga Toxin-Producing E. coli Infection in Humans

Escherichia coli serogroups O5, O15, O26, O45, O55, O76, O91, O103, O104, O111, O113, O118, O121, O123, O128, O145, O146, O157, O165, O172, and O177 are the O-antigen forms of the most clinically relevant Shiga toxin-producing E. coli (STEC) serotypes. In this study, three multiplex PCR assays able to specifically detect these 21 serogroups were developed and validated. For this purpose, the O-antigen gene clusters of E. coli O5 and O76 were fully sequenced, their associated genes were identified on the basis of homology, and serogroup-specific primers were designed. After preliminary evaluation, these two primer pairs were proven to be highly specific and suitable for the development of PCR assays for O5 and O76 serogroup identification. Specific primers were also designed for serogroups O15, O45, O55, O91, O104, O113, O118, O123, O128, O146, O157, O165, O172, and O177 based on previously published sequences, and previously published specific primers for serogroups O26, O103, O111, O121, and O145 were also included. These 21 primer pairs were shown to be specific for their target serogroup when tested against E. coli type strains representing 169 known O-antigen forms of E. coli and Shigella and therefore suitable for being used in PCR assays for serogroup identification. In order to validate the three multiplex PCR assays, 22 E. coli strains belonging to the 21 covered serogroups and 18 E. coli strains belonging to other serogroups were screened in a double-blind test and their sensitivity was determined as 1 ng chromosomal DNA. The PCR assays developed in this study could be a faster, simpler, and less expensive strategy for serotyping of the most clinically relevant STEC strains in both clinical microbiology and public health laboratories, and so their development could benefit for clinical diagnosis, epidemiological investigations, surveillance, and control of STEC infections.