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1.
A molecular phylogeny of the subfamily Cyrtandroideae represented by five genera of four tribes was constructed using sequence analysis of the internal transcribed spacers (ITS) and partial 5.8 S rRNA gene (3’end) of nuclear ribosomal DNA. Direct PCR sequencing method was used in the study. The sequences of ITS-1 in the five species range from 234 bp to 258 bp in size and those of ITS-2 from 218 bp to 246 bp. The ITS-1 (258 bp) and ITS-2 (218 bp) of Whytockia bijieensis differ greatly from those of the other species in size, sequence and G + C content, and therefore the tribe Klugieae represented by W. bijieensis may have diverged from the ancestor of the subfamily Cyrtandroideae at a very early time. In PAUP analysis, W. bijieensis was used as the functional outgroup, and only one most parsimonious Fitch tree was obtained through exhaustive search. The tree has 353 steps, with CI = 0. 932 and RI = 0. 529. In the tree, Chirita crassifolia is basal to a monophyletic group comprising Cyrtandra umbellifera, Briggisia longipes and Anna mollifolia, and the monophyletic group is strongly supported by the bootstrap value (97). The tribes Trichosporeae and Cyrtandreae represented respectively by Anna mollifolia and Cyrtandra urnbellifera both evolved from the tribe Didymorcarpeae, which can explain why many intermediate taxa exist among the three tribes. According to this, the present authors suggest that the tribe Trichosporeae and the tribe Cyrtandreae be merged with the tribeDidymocarpeae.  相似文献   

2.
木犀科系统研究中过氧化物同工酶的应用   总被引:7,自引:0,他引:7  
应用聚丙烯酰胺凝电泳分析了木犀科7属51种(亚种,变种及某些被归并的种)植物叶片过氧化物同工酶。研究结果表明,尽管个别种的种内酶谱有变化,但各个种都有能与其他种相区别的酶谱,各属也具有其特征酶谱,过氧化物同工酶适宜的作为木犀科分类的一个重要指标。根据酶谱认为不分亚科,各族独立为宜,酶谱支持雪柳属和连翘属分别从族及丁香族中独立出来单独建族;支持撤消丁香族,将丁香属并入木犀榄族而靠近女贞属,根据酶谱及  相似文献   

3.
4.
The higher level relationships within Apiaceae (Umbelliferae) subfamily Apioideae are controversial, with no widely acceptable modern classification available. Comparative sequencing of the intron in chloroplast ribosomal protein gene rpl16 was carried out in order to examine evolutionary relationships among 119 species (99 genera) of subfamily Apioideae and 28 species from Apiaceae subfamilies Saniculoideae and Hydrocotyloideae, and putatively allied families Araliaceae and Pittosporaceae. Phylogenetic analyses of these intron sequences alone, or in conjunction with plastid rpoC1 intron sequences for a subset of the taxa, using maximum parsimony and neighbor-joining methods, reveal a pattern of relationships within Apioideae consistent with previously published chloroplast DNA and nuclear ribosomal DNA ITS based phylogenies. Based on consensus of relationship, seven major lineages within the subfamily are recognized at the tribal level. These are referred to as tribes Heteromorpheae M. F. Watson & S. R. Downie Trib. Nov., Bupleureae Spreng. (1820), Oenantheae Dumort. (1827), Pleurospermeae M. F. Watson & S. R. Downie Trib. Nov., Smyrnieae Spreng. (1820), Aciphylleae M. F. Watson & S. R. Downie Trib. Nov., and Scandiceae Spreng. (1820). Scandiceae comprises subtribes Daucinae Dumort. (1827), Scandicinae Tausch (1834), and Torilidinae Dumort. (1827). Rpl16 intron sequences provide valuable characters for inferring high-level relationships within Apiaceae but, like the rpoC1 intron, are insufficient to resolve relationships among closely related taxa.  相似文献   

5.
Aeschynanthus (Gesneriaceae) is a large genus of tropical epiphytes that is widely distributed from the Himalayas and China throughout South-East Asia to New Guinea and the Solomon Islands. Polymerase chain reaction (PCR) consensus sequences of the internal transcribed spacers (ITS) of Aeschynanthus nuclear ribosomal DNA showed sequence polymorphism that was difficult to interpret. Cloning individual sequences from the PCR product generated a phylogenetic tree of 23 Aeschynanthus species (two clones per species). The intraindividual clone pairs varied from 0 to 5.01%. We suggest that the high intraindividual sequence variation results from low molecular drive in the ITS of Aeschynanthus. However, this study shows that, despite the variation found within some individuals, it is still possible to use these data to reconstruct phylogenetic relationships of the species, suggesting that clone variation, although persistent, does not pre-date the divergence of Aeschynanthus species. The Aeschynanthus analysis revealed two major clades with different but overlapping geographic distributions and reflected classification based on morphology (particularly seed hair type).  相似文献   

6.
The 'didymocarpoid Gesneriaceae' (traditional subfam. Cyrtandroideae excluding Epithemateae) are the largest group of Old World Gesneriaceae, comprising 85 genera and 1800 species. We attempt to resolve their hitherto poorly understood generic relationships using three molecular markers on 145 species, of which 128 belong to didymocarpoid Gesneriaceae. Our analyses demonstrate that consistent topological relationships can be retrieved from data sets with missing data using subsamples and different combinations of gene sequences. We show that all available classifications in Old World Gesneriaceae are artificial and do not reflect natural relationships. At the base of the didymocarpoids are grades of clades comprising isolated genera and small groups from Asia and Europe. These are followed by a clade comprising the African and Madagascan genera. The remaining clades represent the advanced Asiatic and Malesian genera. They include a major group with mostly twisted capsules. The much larger group of remaining genera comprises exclusively genera with straight capsules and the huge genus Cyrtandra with indehiscent fruits. Several genera such as Briggsia, Henckelia, and Chirita are not monophyletic; Chirita is even distributed throughout five clades. This degree of incongruence between molecular phylogenies, traditional classifications, and generic delimitations indicates the problems with classifications based on, sometimes a single, morphological characters.  相似文献   

7.
Eva Luegmayr 《Grana》2013,52(4-5):221-232
Pollen of 108 species out of 18 genera (from all tribes of the Old World Gesneriaceae [subf. Cyrtandroideae]) was examined using light, scanning and transmission electron microscopy. The pollen grains are small sized, isopolar and 3-colpate or 3-colporate. In equatorial view they are mostly spheroidal (rarely suboblate or oblate), in polar view circular or subangular. The most variable character is the exine structure and -sculpture. The tectum is perforate, microreticulate, coarsely reticulate or rugulate. Further important characters of the tectum are (a) the presence or absence of conical supratectate sculptural elements, and (b) the width of lumina being either equal or exhibiting different at the apo- and mesocolpium. Ten exine types are distinguished. Some genera and species can be well referred to a special exine type, e.g., Aeschynanthus, Epithema, Stauranthera grandiflora; in other genera several exine types occur, e.g., in the large and heterogeneous genus Didymocarpus. The pollen morphology of the two large subfamilies Cyrtandroideae and Gesnerioideae is compared.  相似文献   

8.
中国菊科植物的系统分类与区系的初步研究   总被引:29,自引:2,他引:29  
林有润 《植物研究》1997,17(1):6-27
为1993年"菊科植物的系统分类与区系地理的初步探讨"(世界)一文的姊妹篇,重点论述我国菊科的系统分类及其区系地理成分。文中介绍了分布我国的菊科240属隶于2亚科、5超族、11族中的系统位置。论述了我国菊科植物区系地理成分的特点是:1.大洲间共同分布或洲际间断分布的属多,且具明显的热带亲缘;2.与亚洲国家,包括中亚国家或亚洲热带国家共同分布的属多,尤其是成"中亚-青藏高原-喜马拉雅山"地区分布的属多;3.中国特有属多,其中我国西南省区特有属最多。文中还讨论了分布我国菊科各族祖先种的起源、迁移以及我国区系地理热带亲缘和"横断山脉-喜马拉雅山脉(东)森林植物亚区"菊科植物分布的特点。  相似文献   

9.
毛茛科金莲花亚科植物的地理分布   总被引:11,自引:1,他引:10  
本文对毛茛科金莲花亚科各属的地理分布作了分析,该亚科植物除了少数属的一些种分布到南半球的温带地区,一些种分布或延伸到亚热带山地、非洲东部和北部的干旱、半干旱的地区外,绝大部分的属、种均分布于泛北极区域。根据其17个属的地理分布式样,把它们划分为8个分布区类型:(1)北温带分布类型4属;(2)北温带和非洲分布类型1属;(3)北半球温带和南半球间断分布类型1属;(4)欧洲和东亚间断分布类型1属;(5)西亚分布类型1属;(6)地中海分布类型3属;(7)欧亚和温带亚洲分布类型1属;(8)东亚分布类型5属。本文以形态特征为主,结合花粉和染色体的性状分析,认为东亚特有的鸡爪草属、Megaleranthis和铁破锣属可能分别是联系驴蹄草属和金莲花属,鸡爪草属和金莲花属以及金莲花族和升麻族的中间类型。另外,文中详细地统计了该亚科的不同等级分类群及特有种在各个植物区的分布,并从系统发育的观点讨论了各个植物区所具有的原始类群和进化类群,提出了如下论点,即东亚植物区(特别是中国西南部)不但是金莲花亚科植物分布的多度和多样性中心以及特有类群的分布中心,而且还是原始类群的保存中心,伊朗-土兰区及地中海周围是第二分布中心。  相似文献   

10.
重庆市种子植物区系特征分析   总被引:2,自引:0,他引:2  
对重庆市种子植物区系进行了研究,其区系特征如下:(1)植物种类和区系组成丰富,共分布有野生种子植物208科1 127属4 764种,其科包含12种分布型和13个变型,属包含15种分布型和23个变型;(2)科的区系组成以热带成分占主要,总共包含83科,达到重庆地区种子植物总科数的39.90%,这说明重庆种子植物区系带有一定的热带亲缘关系.属的区系组成以热带成分最多,达到454属,占重庆市种子植物总属数的40.28%,表明重庆地区种子植物区系的热带亲缘关系较强;(3)特有现象明显,虽然本地区分布的特有科属相对较少,但特有种丰富.  相似文献   

11.
Two morphogenetic patterns have contributed to phylogenetic diversification within the Gesneriaceae: accrescence of one of the paired cotyledons (anisocotyly), which serves to differentiate the subfamily Cyrtandroideae; sustained growth of the accrescent cotyledon accompanied by prolonged suppression and displacement of the embryonic apical meristem, which gives rise to an acaulescent, dorsiventral vegetative plant body (phyllomorph) and further serves to differentiate species of Cyrtandroideae found in two tribes and several genera including Streptocarpus. It was possible to prevent cotyledonary accrescence and induce caulescence at will, either by supplying exogenous GA3 or inhibiting auxin transport in species of Streptocarpus that normally manifest an extreme, phyllomorphic morphology. It was also possible to induce sustained, phyllomorphic development of cotyledons that are normally non-accrescent with exogenous cytokinin. Therefore morphogenetic capacities previously thought to be “lost” or “lacking” in subgenus Streptocarpus and, with respect to isocotyly, the tribe Cyrtandroideae, are, in fact, present but suppressed. An hypothesis regarding the role of hormones with respect to morphogenesis and phylogeny of Streptocarpus is suggested.  相似文献   

12.
梧桐科植物的地理分布   总被引:5,自引:0,他引:5  
梧桐科植物全世界有60属约1546种,主要分布在热带和亚热带地区,只有少数种类可分布至温带地区,由于梧桐科是多型的科,科的范围较大,对有些属是否应隶属于该科,国内外学者的意见很不一致。本文基本上按照J.Hutchinson系统和参考有关文献对一些属的分类位置作了调整,把梧桐科分为12族,根据A.Takhtajan的世界植物区系区划的原则,将梧桐植物在世界上的分布区,划分为6区8亚区23地区,并指出各属在中国各省区的地理分布,现在中国梧桐科植物连引种栽培的在内共有25属99种7变种,其中野生的有18属85种7变种,引种栽培的有8属14种,对梧桐科植物的起源和发展作了一些探讨。  相似文献   

13.
The present paper deals with the following three aspects: 1. It attempts to discuss the problems on primitive forms of the family Araliaceae. The genus Tupidanthus Hook. f. & Thoms. was considered by H. Harms (1894) and H. L. Li (1942) as primitive, whilst another genus Plerandra A. Gray was regarded as primitive by R. H. Eyde & C. C. Tseng in 1971. Having made a detailed comparison of the taxonomical characters of these two genera, the present authors believe that both genera are not the most primitive in the Araliaceae. Their affinit yis not close enough and they possibly evolved in parallel lines from a common ancestor which is so far unknown yet. 2. By studying the systems of the past, the present authors believe that none of them is entirely satisfactory. Bentham (1867) recognized five ‘series’ (in fact, equivalent to ‘tribe’ with the ending-eae of names) based on the petaline arrangement in the bud, the numbers of stamen and the types of endospem. This is a plausible fundamental treatment for the Araliaceae, but choosing the endosperm as a criteria in dividing tribe is artifical. As we know today, both ruminate and uniform endosperm are usually presente in the same genus. Seemann’s system (1868) divided the Hederaceae (excl. Trib. Aralieae) into five tribes, in addition to the locules of ovary. The criteria are essentially the same as Bentham’s. The system of Hams (1894) divided the family into three tribes. Two tribes, Aralieae and Mackinlayeae, of Bentham are retained, but other groups were combined in the Trib. Schefflereae. However, Harms did not retain one of those three oldest legitimate names which had named by Bentham, that is contrary to the law of priority in the International Code of Botanical Nomenelature. Hutchinson (1967) adopted seven tribes for the family. The criteria essentially follow those of Bentham, but the inflorescence is overstressed. The inflorescence is an artifical taxonomical character in dividing tribes, because of some dioecious plants, such as Meryta sinclairii (Hook. f.) Seem., have two types of inflorescence in male and female plants. According to Hutchinson’s arrangement, the male and female plants would be put in separate tribes. 3. The present authors are of the opinion that in the study of a natural classification of plant groups emphasis should be laid not only on the characters of the reproductive organs, but on those of vegetative organs as well. The present revised system is based principally upon the characters of both flowers and leaves of the five tribes as follows: Trib. 1. Plerandreae Benth. emend. Hoo & Tseng Trib. 2. Tetraplasandreae Hoo & Tseng Trib. 3. Mackinlayeae Benth. Trib. 4. Aralieae Benth. Trib. 5. Panaceae Benth. emend. Hoo & Tseng  相似文献   

14.
During the Early Cretaceous, ocean-floor spreading gradually opened up the tropical Atlantic and the Indian Ocean basin widened as the eastern segments of Gondwanaland were conveyed farther apart. At the same time, epeiric seas were advancing on all continents, reaching maximum extent during the Cenomanian. The resultant trend to widespread, more equable climate favored the invasion into the lowlands of angiosperms whose postulated origin was in mild uplands at low latitudes during pre-Cretaceous times. As tropical and subtropical lands were rafted farther apart by ocean-floor spreading following Albian-Cenomanian times, new taxa (species, genera, tribes, families) evolved in isolation. This accounts in part for the increasing richness of the three major tropical floras following the Cretaceous. Changes in Mesozoic paleogeography also appear to clarify several other puzzling aspects of early angiosperm history and distribution, including their early appearance at middle latitudes.  相似文献   

15.
青海鹅观草属的叶片表皮微形态特征及其分类意义的探讨   总被引:3,自引:0,他引:3  
通过青海鹅观草属叶片表皮的解剖观察,结合外部形态,表明了该属植物在小麦族中共族分属的合理性,同时对青海地区属下类群重新进行了确认,共划分2组16种,即拟技碱草组,包括6种;弯穗草组,包括10种.过去处理的种短柄鹅观草和多秆鹅观革分别作为短颖鹅观草和缘毛鹅观草的变种。此外,类群间的演化水平和属的地理起源也作了初步探讨。  相似文献   

16.
棕榈科植物的地理分布   总被引:9,自引:0,他引:9  
棕榈科是一个泛热带分布的科,共有198属,约2670种,下分6亚科,14族。贝叶棕族是最原始的族,低地榈族则最进化。本科植物在世界上的分布可划分为13个区,其中以印度-马来西区和新热带区的属、种最多。中国只有16属和85种,没有特有属。这些种大部分属热带亚洲分布,与热带亚洲植物区系关系非常密切。关于棕榈科起源地问题,有西冈瓦纳起源和劳亚起源之说。根据化石记录和形态特征的分析,棕榈科很可能于早白垩纪  相似文献   

17.
The distribution of marine bivalve species among genera and higher taxa takes the form of the classic hollow curve, wherein few lineages are species rich and many are species poor. The distribution of species among genera (S/G ratio) varies with latitude, with temperate S/G's falling within the null expectation, and tropical and polar S/G's exceeding it. Here, we test several hypotheses for this polar overdominance in the species richness of small numbers of genera. We find a significant positive correlation between the latitudinal range of a genus and its species richness, both globally and within regions. Genus age and species richness are also positively related, but this relationship breaks down when the analysis is limited to genera endemic to climate zones or with narrow latitudinal ranges. The data suggest a link between speciation and range-expansion, with genera expanding out of the tropical latitudinal bins tending to speciate more prolifically, both globally and regionally. These genera contain more species within climate zones than taxa endemic to that zone. Range expansion thus appears to be fundamentally coupled with speciation, producing the skewed distribution of species among genera, both globally and regionally, whereas clade longevity is achieved through extinction -- resistance conferred by broad geographical ranges.  相似文献   

18.
The Malpighiaceae are a family of ~1250 species of predominantly New World tropical flowering plants. Infrafamilial classification has long been based on fruit characters. Phylogenetic analyses of chloroplast DNA nucleotide sequences were analyzed to help resolve the phylogeny of Malpighiaceae. A total of 79 species, representing 58 of the 65 currently recognized genera, were studied. The 3' region of the gene ndhF was sequenced for 77 species and the noncoding intergenic spacer region trnL-F was sequenced for 65 species; both sequences were obtained for the outgroup, Humiria (Humiriaceae). Phylogenetic relationships inferred from these data sets are largely congruent with one another and with results from combined analyses. The family is divided into two major clades, recognized here as the subfamilies Byrsonimoideae (New World only) and Malpighioideae (New World and Old World). Niedenzu's tribes are all polyphyletic, suggesting extensive convergence on similar fruit types; only de Jussieu's tribe Gaudichaudieae and Anderson's tribes Acmanthereae and Galphimieae are monophyletic. Fleshy fruits evolved three times in the family and bristly fruits at least three times. Among the wing-fruited vines, which constitute more than half the diversity in the family, genera with dorsal-winged samaras are fairly well resolved, while the resolution of taxa with lateral-winged samaras is poor. The trees suggest a shift from radially symmetrical pollen arrangement to globally symmetrical pollen at the base of one of the clades within the Malpighioideae. The Old World taxa fall into at least six and as many as nine clades.  相似文献   

19.
高黎贡山兰花的多样性   总被引:4,自引:0,他引:4  
对高黎贡山兰科植物的生物地理学和多样性进行了研究。1.兰科是高黎贡山种子植物中最大的科,包括75属265种。2.高黎贡山兰花起源于新、旧世界的热带和温带, 热带属占60%(45属),温带属占38.67%(29属),包括2个云南特有属。但是,高黎贡山兰科植物与地中海地区和中亚地区的联系十分微弱。3.高黎贡山的兰花以地生兰为主。这里,57.33%(43属)为地生兰,而附生兰和腐生兰仅分别为31属和3属。4.兰花物种的分布区式样表明高黎贡山兰花以温带兰为主 温带兰占总种数的69.43%(184种),包括东亚成分即滇西高黎贡山-东喜马拉雅分布的种和中国西南部特有种,它们是高黎贡山兰花区系的核心。5.高黎贡山兰科的特有现象在于1)具有云南二个特有属蜂腰兰Bulleyia和反唇兰Smithorchis;2)有高黎贡山特有种21个,如泸水兜兰Paphiopedilum markianum,贡山风兰Cymbidium gongshanense,贡山贝母兰Coelogyne gongshanense,热带附生兰——万带兰亚科在高黎贡山没有形成特有种;3)高黎贡山北段的特有种比南段丰富贡山有14种,腾冲仅有4种; 海拔1800~2100 m的梯度带特有种最多(13种);4)高黎贡山有云南特有种10种,其中小花槽舌兰Holcoglossum junceum是一个热带种,因为板块位移而来到了亚热带地域;5)高黎贡山的兰科植物中有19.25%(51种)是中国特有种,它们出现在高黎贡山,分布在云南其他地区和西南的一些省区。高黎贡山特有种,分布到高黎贡山的云南特有种和分布到高黎贡山的中国特有种一共为82种,占高黎贡山兰科总种数的30.91%, 兰科在高黎贡山是一个特有化程度很高的类群。  相似文献   

20.
Bignoniaceae are woody, trees, shrubs, and lianas found in all tropical floras of the world with lesser representation in temperate regions. Phylogenetic analyses of chloroplast sequences (rbcL, ndhF, trnL-F) were undertaken to infer evolutionary relationships in Bignoniaceae and to revise its classification. Eight clades are recognized as tribes (Bignonieae, Catalpeae, Coleeae, Crescentieae, Jacarandeae, Oroxyleae, Tecomeae, Tourrettieae); additional inclusive clades are named informally. Jacarandeae and Catalpeae are resurrected; the former is sister to the rest of the family, and the latter occupies an unresolved position within the "core" Bignoniaceae. Tribe Eccremocarpeae is included in Tourrettieae. Past classifications recognized a large Tecomeae, but this tribe is paraphyletic with respect to all other tribes. Here Tecomeae are reduced to a clade of approximately 12 genera with a worldwide distribution in both temperate and tropical ecosystems. Two large clades, Bignonieae and Crescentiina, account for over 80% of the species in the family. Coleeae and Crescentieae are each included in larger clades, the Paleotropical alliance and Tabebuia alliance, respectively; each alliance includes a grade of taxa assigned to the traditional Tecomeae. Parsimony inference suggests that the family originated in the neotropics, with at least five dispersal events leading to the Old World representatives.  相似文献   

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