首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 46 毫秒
1.
查阅保存于英国爱丁堡植物园标本馆(E)、华南植物园标本馆(IBSC)、邱园植物标本馆(K)、法国巴黎自然历史博物馆植物标本馆(P)和奥地利维也纳大学植物标本馆(WU)的荨麻科(Urticaceae)标本,发现在楼梯草属(Elatostema J.R.Forster & G.Forster)中有23种8变种的名称在原始描述中没有引证明确的标本,或引证有2份或2份以上的标本,但没指定模式.根据<国际植物命名法规>9.4、9.9和9.10,以及辅则9A.1、9A.2、9A.3和9A.4的精神,对这些名称做出后选模式指定.  相似文献   

2.
报道荨麻科楼梯草属7种1变种植物在我国6个省区分布的新记录,其中广西分布新记录的有算盘楼梯草和多歧楼梯草,贵州分布新记录的有曲毛楼梯草,海南分布新记录的有锐齿楼梯草和深绿楼梯草,湖南分布新记录的有短毛楼梯草,四川分布新记录的有丝梗楼梯草,云南分布新记录的有细角楼梯草。  相似文献   

3.
楼梯草属植物的瘦果具有较高的形态多样性,可作为种类鉴定的重要依据.然而,中国超过半数楼梯草属植物缺少瘦果形态信息.该研究通过野外考察、标本查阅以及光镜和扫描电镜的观察,对七种楼梯草属植物的瘦果进行了补充描述,并提供了墨线图和照片.该研究结果对该属的进一步分类修订提供了有价值的信息.  相似文献   

4.
楼梯草属植物的瘦果具有较高的形态多样性,可作为种类鉴定的重要依据。然而,中国超过半数楼梯草属植物缺少瘦果形态信息。该研究通过野外考察、标本查阅以及光镜和扫描电镜的观察,对七种楼梯草属植物的瘦果进行了补充描述,并提供了墨线图和照片。该研究结果对该属的进一步分类修订提供了有价值的信息。  相似文献   

5.
中国楼梯草属(荨麻科)几种植物的订正   总被引:1,自引:0,他引:1  
根据对中国楼梯草属Elatostema植物标本的研究,将碧江楼梯草E.bijiangense归并入楼梯草E. involucratum,长叶墨脱楼梯草E.medogense var.oblongum和树志楼梯草E.shuzhii归并入墨脱楼梯草E. medogense,光茎钝叶楼梯草E.obtusum var.glabrescens归并入三齿钝叶楼梯草E.obtusum var.trilobula- tum,三裂楼梯草E.sinense var.trilobatum归并入对叶楼梯草E.sinense,赤水楼梯草E.strigulosum var.semitripilinerve归并入伏毛楼梯草E.strigulosum。  相似文献   

6.
国产赖草属的分类修订   总被引:2,自引:0,他引:2  
蔡联炳  苏旭 《植物研究》2007,27(6):651-660
通过标本研究和野外考察,对中国赖草属(Leymus Hochst.)进行了分类修订。结果在中国共确认了3组、33种、7变种赖草属植物,其中多穗组包含4种,少穗组包含24种、7变种,单穗组包含5种,新报道的3个种和新修订的4个类群(即3个新组合和1个新名称)皆隶于少穗组。同时对赖草属的研究简史、属的形态特征和一些类群的地理分布也分别作了简要介绍。  相似文献   

7.
描述了采自云南省东南部楼梯草属一新种——柳叶楼梯草(Elatostemaneriifolia)和据其为模式建立的一新系——柳叶楼梯草系(ser.Neriifolia),并讨论了这些新类群和相近类群在形态上的区别,并对柳叶楼梯草的保护等级进行了评估。  相似文献   

8.
王文采 《植物研究》1992,12(3):205-212
在本文中2种名和2变种名被作为异名;Boehmeria delavayiGagnep.被证实为雾水葛属植物,降级作为雅致雾水葛的变种;Pellioniatrichosantha Gagnep.的采自云南东北部的合模式乃是属于楼梯草属的植物;4种和2变种的地理分布扩大。  相似文献   

9.
云南东南部赤车属和楼梯草属研究随记   总被引:1,自引:0,他引:1  
王文采 《植物研究》2006,26(1):15-24
描述了云南东南部荨麻科楼梯草属5个新种和3个新变种;报导了赤车属1个种和楼梯草属3个种在云南的新分布。  相似文献   

10.
云南楼梯草属研究随记   总被引:5,自引:1,他引:4  
王文采 《植物研究》2003,23(3):257-260
描述了云南荨麻科楼梯草属三新种和一新变种;列出了勐仑楼梯草与骤尖楼梯草的区别特征,据此说明勐仑楼梯草是一个比骤尖楼梯草原始的独立种,不赞同将其归并,而认为应予以恢复。  相似文献   

11.
12.
13.
14.
It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.  相似文献   

15.
16.
Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.  相似文献   

17.
Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.  相似文献   

18.
肝癌中HBV和HCV基因和抗原的分布及意义   总被引:1,自引:0,他引:1  
采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细  相似文献   

19.
20.
For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号