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1.
最近被重新界定的广义石山苣苔属(Petrocodon Hance)是苦苣苔科(Gesneriaceae)一个中等大小的属,我国目前已知的有34种1变种,主要分布于我国华南至西南石灰岩地区。该文报道了于云南东南部马关县发现的该属一新种——细管石山苣苔(Petrocodon tenuitubus W. H. Chen,F. WenY. M. Shui)。该新种在形态上与陆氏细筒苣苔(P. lui)、细筒苣苔(P. hispidus)和长檐苣苔(P. jasminiflorus)相似,但其线形或披针形的苞片和小苞片均为3枚,花冠筒细小且弯曲,盘形柱头1,很容易区别于陆氏细筒苣苔和细筒苣苔;而其叶片卵形至圆形,花冠裂片卵形而尖端钝以及退化雄蕊3,则显著区别于长檐苣苔。该新种的发现对推进我国石灰岩地区苦苣苔科植物资源的发掘具有一定意义。主模式标本存放于中国科学院昆明植物研究所标本馆(KUN),等模式标本存放于广西植物研究所标本馆(IBK)。 相似文献
2.
河北省苔类植物新纪录属的研究—I.耳叶苔属(Frullania Raddi) 总被引:1,自引:0,他引:1
在研究标本和文献的基础上,对河北省苔类植物新纪录属-耳叶苔属Frullania Raddi进行了首次报道,其中包括达乌里耳叶苔F.davurica、达乌里耳叶苔凹叶变种F.davuricavar.concava、石生耳叶苔F.inflata、盔瓣耳叶苔F.muscicola、陕西耳叶苔F.schensiana、塔拉大克耳叶苔F.taradakensis、远东耳叶苔F.fauriana和筒瓣耳叶苔F.diversitexta等7种1变种。本文对它们的生境和地理分布作了初步讨论,并编制了河北省耳叶苔属植物的分种检索表。 相似文献
3.
在研究标本和文献的基础上,对河北省苔类植物新纪录属--耳叶苔属Frullania Raddi进行了首次报道,其中包括达乌里耳叶苔F. davurica、达乌里耳叶苔凹叶变种F. davurica var. concava、石生耳叶苔F. inflata、盔瓣耳叶苔F. muscicola、陕西耳叶苔F. schensiana、塔拉大克耳叶苔F. taradakensis、远东耳叶苔F. fauriana和筒瓣耳叶苔F. diversitexta等7种1变种。本文对它们的生境和地理分布作了初步讨论,并编制了河北省耳叶苔属植物的分种检索表。 相似文献
4.
石山苣苔属(苦苣苔科)约41种,主要分布于我国西南石灰岩地区。到目前为止,仅其中四种的染色体数目被研究和报道,其余绝大多数物种的染色体数目和倍性尚不清楚,染色体数目和倍性在该属及其姐妹属报春苣苔属中的演变历史及其对两属物种多样性分化的影响亦不清楚。该文以叶片水培生根法获取的四种(含一变种)石山苣苔属植物 [即石山苣苔原变种(Petrocodon dealbatus var. dealbatus)、齿缘石山苣苔(Petrocodon dealbatus var. denticulatus)、弄岗石山苣苔(Petrocodon longangensis)、石山苣苔未定名种(Petrocodon sp.)]的根尖细胞为材料开展染色体实验,探索了多种不同的实验条件对染色体制片效果的影响并获取染色体数目,在石山苣苔属和报春苣苔属的系统树上追踪了染色体数目和倍性的演变历史,同时探讨染色体数目尤其是倍性变化是否对两属物种多样性分化存在影响。结果表明:(1)长度为1~1.5 cm的根尖,0.002 mol·L-1 8-羟基喹啉溶液预处理5 h,解离4 min为较适宜的染色体制备条件。(2)四种(含一变种)石山苣苔属植物染色体数目一致,均为二倍体(2n=2x=36)。(3)两属之间及两属各自的最近共同祖先染色体数目尚不能确定,除个别物种染色体条数或倍性有变化以外,其余已知染色体数目的物种均为2n=2x=36,在两属中高度一致,石山苣苔属与报春苣苔属物种多样性分化尤其两属物种多样性巨大差异与染色体数目和基因组倍性变化无关。综上结果为石山苣苔属植物及其近缘类群染色体制备提供了参考,也为进一步对该类群的分类、系统演化和物种形成等方面的研究提供了基础数据和启示。 相似文献
5.
异叶苣苔属(苦苣苔科)的核型研究 总被引:4,自引:0,他引:4
本文首次报道了中国特有异叶苣苔属的染色体数目及核型。该属所研究种类的染色体数目均为
2n=18,染色体长度在2.0µm以上,在尖舌苣苔族所报道的染色体中显示出较原始的性状。尖舌苣苔
族的染色体基数可能是x=9。异叶苣苔属的间期核均为复杂型;前期染色体呈渐变型。核型从对称型
向不对称型的演化主要表现在近中部着丝粒,尤其是近端部着丝粒染色体比例的增大。毕节异叶苣苔
W.bljieensis和峨眉异叶苣苔W.tsiangiana var.wilsonii的核型分别为2n=2m+8m+8sm(1sat)和
2n=2m+8m(1sat)+8sm(2sat),较为对称。紫红异叶苣苔W.purpurascens和白花异叶苣苔W.
tsiangiana var. tsiangiana的核型分别为2n=4m+6sm+8st(1sat)和2n=4m+8sm(2sat)+6st,比较
特化。河口异叶苣苔W.hekouensis的核型是2n=4m+10sm(1sat)+4st,处于二者之间。峨眉异叶苣
苔和原变种白花异叶苣苔的核型差异较大,在外部形态方面二者之间的性状变异也间断较大。本文建 议将该变种从白花异叶苣苔W.tsiangiana中移出自成一种,并和毕节异叶苣苔近缘。 相似文献
6.
报道了在广西发现的苦苣苔科异裂苣苔属一新变种,即粉绿异裂苣苔Pseudochirita guangxiensis (S. Z. Huang) W. T. Wang var. glauca Y. G. Wei & Yan Liu。它与原变种的区别在于叶近全缘或有不明显的钝锯齿,茎和叶背、叶面密被近贴伏的绒毛,花冠外疏被腺毛。 相似文献
7.
直瓣苣苔属、筒花苣苔属和吊石苣苔属4个种的核形态学研究 总被引:7,自引:0,他引:7
本文报道了苦苣苔科直瓣苣苔属Ancylostemon、筒花苣苔属Briggsiopsis和吊石苣苔属Lysionotus
中4个种的染色体数目和核形态。凹瓣苣苔A.aureus的染色体数目为n=34,与其近缘种凸瓣苣苔
A.convexus的染色体数目相同。该种的核型公式为2n=20m(1sat)+14sm,核型类型属于2A。间期核
为复杂染色中心型(complex chromocenter type);细胞有丝分裂前期的染色体为近基型(proximal type)
我国特有单种属筒花苣苔属Briggsiopsis的间期核为简单—复杂染色中心型(simple-complex chromocenter
type);细胞有丝分裂前期的染色体为中间—渐变型(interstitial—gradient type);核型公式为2n=34=25m
+6sm+3st,与近缘类群——粗筒苣苔属Briggsia染色体数目2n=34,68相比,无论染色体数目还是核
型均显示比较原始的特征。吊石苣苔属的蒙自吊石苣苔L.carnosus和翅茎吊石苣苔L.serratus D.
Don var.pterocaulis的核型公式分别是2n=30=21m+5sm+3st+1t和2n=32=21m+10sm+1t。核
型类型分别属于2A和2B。间期核均为简单—复杂染色中心型(simple-complex chromocenter type);细胞 有丝分裂前期的染色体为渐变型(gradient type)。 相似文献
8.
记载了广西苦苣苔科一新变种——翅茎半蒴苣苔Hemiboea subcapitata Clarke var. pterocaulis Z. Y. Li。该变种与原变种不同在于茎具翅,花期较早。 相似文献
9.
在对中国吉林长白山产苔类全萼苔科无齿全萼苔(Gynmomitrium uncrenulatum C.Gaoet K.C.Chang)和锐裂钱袋苔小叶变种(Marsupella commutata var.microfolia K.C.Chang)的模式标本进行了研究,对比发现无齿全萼苔和锐裂钱袋苔小叶变种与锐裂钱袋苔特征相一致,将其处理为锐裂钱袋苔的异名。 相似文献
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12.
《Cryptogamie Bryologie ☆》1999,20(3):203-206
Andreaea megistospora B. Murray is newly reported for Spain. New sites are reported for Ulota calvescens Wils., Tayloria tenuis (With.) Schimp., Metzgeria temperata Kuwah. and Frullania oakesiana Aust., very rare species in the Iberian Peninsula. Dicranum crassifolium Sérgio, Ochyra & Séneca is reported for Galicia. 相似文献
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15.
Law Yuh-Wu 《植物分类学报:英文版》1984,22(2):89-109
A new system of classification of Magnoliaceae proposed. This paper deals mainly with taxonomy and phytogeography of the family Magnoliaceae on the basis of external morphology, wood anatomy and palynology. Different authors have had different ideas about the delimitation of genera of this family, their controversy being carried on through more than one hundred years (Table I). Since I have been engaged
in the work of the Flora Reipublicae Popularis Sinicae, I have accumulated a considerable amount of information and material and have investigated the living plants at their natural localities, which enable me to find out the evolutionary tendencies and primitive morphological characters of various genera of the family. According to the evolutionary tendencies of the characters and the geographical distribution of this family I propose a
new system by dividing it into two subfamilies, Magnolioideae and Liriodendroideae Law (1979), two tribes, Magnolieae and Michelieae Law, four subtribes, Manglietiinae Law, Magnoliinae, Elmerrilliinae Law and Micheliinae, and fifteen genera (Fig. 1 ), a system which is different from those by J. D. Dandy (1964-1974) and the other authors.
The recent distribution and possible survival centre of Magnoliaceae. The members of Magnoliaceae are distributed chiefly in temperate and tropical zones of the Northern Hemisphere, ——Southeast Asia and southeast North America, but a few genera and species also occur in the Malay Archipelago and Brazil of the Southern Hemisphere. Forty species of 4 genera occur in America, among which one genus (Dugendiodendron) is endemic to the continent, while about 200 species of 14 genera occur in Southeast Asia, of which 12 genera are endemic. In China there are about 110 species of 11 genera which mostly occur in Guangxi, Guangdong and Yunnan; 58 species and more than 9 genera occur in the mountainous districts of Yunnan. Moreover, one genus
(Manglietiastrum Law, 1979) and 19 species are endemic to this region. The family in discussion is much limited to or interruptedly distributed in the mountainous regions of Guangxi, Guangdong and Yunnan. The regions are found to have a great abundance of species, and the members of the relatively primitive taxa are also much more there than in the other regions of the world.
The major genera, Manglietia, Magnolia and Michelia, possess 160 out of a total of 240 species in the whole family. Talauma has 40 species, while the other eleven genera each contain only 2 to 7 species, even with one monotypic genus. These three major genera are sufficient for indicating the evolutionary tendency and geographical distribution of Magnoliaceae. It is worthwhile discussing their morphological characters and
distributional patterns as follows:
The members of Manglietia are all evergreen trees, with flowers terminal, anthers dehiscing introrsely, filaments very short and flat, ovules 4 or more per carpel. This is considered as the most primitive genus in subtribe Manglietiinae. Eighteen out of a total of 35 species of the genus are distributed in the western, southwest to southeast Yunnan. Very primitive species, such as Manglietia hookeri, M. insignis and M. megaphylla, M. grandis, also occur in this region. They are distributed from Yunnan eastwards to Zhejiang and Fujian through central China, south China, with only one species (Manglietia microtricha) of the genus westwards to Xizang. There are several species distributing southwards from northeast India to the Malay Archipelago (Fig. 7).
The members of Magnolia are evergreen and deciduous trees or shrubs, with flowers terminal, anthers dehiscing introrsely or laterally, ovules 2 per carpel, stipule adnate to the petiole. The genus Magnolia is the most primitive in the subtribe Magnoliinae and is the largest genus of the family Magnoliaceae. Its deciduous species are distributed from Yunnan north-eastwards to Korea and Japan (Kurile N. 46’) through Central
China, North China and westwards to Burma, the eastern Himalayas and northeast
India. The evergreen species are distributed from northeast Yunnan (China) to the
Malay Archipelago. In China there are 23 species, of which 15 seem to be very primitive, e.g. Magnolia henryi, M. delavayi, M. officinalis and M. rostrata, which occur in
Guangxi, Guangdong and Yunnan.
The members of Michelia are evergreen trees or shrubs, with flowers axillary, anthers dehiscing laterally or sublaterally, gynoecium stipitate, carpels numerous or few.
Michelia is considered to be the most primitive in the subtribe Micheliinae, and is to
the second largest genus of the family. About 23 out of a total of 50 species of this
genus are very primitive, e.g. Michelia sphaerantha, M. lacei, M. champaca, and M.
flavidiflora, which occur in Guangdong, Guangxi and Yunnan (the distributional center
of the family under discussion) and extend eastwards to Taiwan of China, southern
Japan through central China, southwards to the Malay Archipelago through Indo-China.
westwards to Xizang of China, and south-westwards to India and Sri Lanka (Fig. 7).
The members of Magnoliaceae are concentrated in Guangxi, Guangdong and Yunnan
and radiate from there. The farther away from the centre, the less members we are
able to find, but the more advanced they are in morphology. In this old geographical
centre there are more primitive species, more endemics and more monotypic genera.
Thus it is reasonable to assume that the region of Guangxi, Guangdong and Yunnan,
China, is not only the centre of recent distribution, but also the chief survival centreof Magnoliaceae in the world. 相似文献
16.
LINDA FUSELIER PAUL G. DAVISON MARIAH CLEMENTS BLANKA SHAW NICOLAS DEVOS JOCHEN HEINRICHS J
RN HENTSCHEL MARKO SABOVLJEVIC PTER SZ
VNYI SCOTT SCHUETTE WOLFGANG HOFBAUER A. JONATHAN SHAW 《Biological journal of the Linnean Society. Linnean Society of London》2009,98(4):745-756
Seed plant genera often exhibit intercontinental disjunctions where different species are found on different continents. Many morphologically circumscribed bryophyte species exhibit similar disjunctions. We used nucleotide sequences from the plastid and nuclear genomes to test hypotheses of phylogeography within representatives of the genus Metzgeria: Metzgeria furcata, Metzgeria conjugata, and Metzgeria myriopoda. The first two species have sexual and asexual populations, exhibit disjunctions between North America and Europe, and have been split into separate species, numerous subspecies or varieties. The third species occurs in eastern North America but is not reported from Europe. Phylogenetic analyses resolved three distinct lineages within the morphologically defined species, M. furcata: one in North America, and two in Europe. Similarly, three morphologically cryptic clades of M. conjugata were resolved by the molecular data: northern North America, Europe, and south‐eastern North America. For both species, molecular divergence among taxa occurred in the absence of morphological change. In the case of M. myriopoda, all plants from eastern North America were both morphologically uniform and genetically homogeneous (although not identical). The present study provides significant insight into a plant group with complex taxonomy, and indicates that these liverwort taxa with wide distributions, extreme sex ratios, and continental disjunctions harbor cryptic lineages. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 98 , 745–756. 相似文献
17.
The diatom family Rhaphoneidaceae is characterized by high generic diversity and low species diversity with most genera known to have long stratigraphic ranges. The genera within this family are neritic marine, and mostly epipsammic. A new modern and epipsammic genus, Meloneis gen. nov., is described herein and is compared to all genera within Rhaphoneidaceae and especially to Rhaphoneis Ehrenberg s.l. Within Meloneis three new species and one variety are distinguished and described herein: M. mimallis sp. nov., M. mimallis var. zephyria var. nov., M. akytos sp. nov., and M. gorgis sp. nov. 相似文献
18.
RICLEF GROLLE MAY LING SO 《Botanical journal of the Linnean Society. Linnean Society of London》2003,142(2):229-235
Riccia fruticulosa O.F.Müll., 1782 from Norway is a valid name, referring to Riccardia palmata (Hedw.) Carruth. In 1785 Dickson misidentified British plants of a blue Metzgeria as R. fruticulosa . The European blue species of Metzgeria is conspecific with M. violacea (Ach.) Dumort., which replaces M. fruticulosa auct. The true origin of the type of Jungermannia violacea Ach., 1805 is probably Tierra del Fuego (rather than Dusky Bay, New Zealand), where the species is widespread. Reports from Australasia, Asia and Africa are all erroneous. The blue colour of Jungermanniales is found only in living plants and is derived from the oil-bodies. In contrast, that of Metzgeria appears only after death; its biological function is unknown. © 2003 The Linnean Society of London, Botanical Journal of the Linnean Society, 2003, 142 , 229−235. 相似文献
19.
<正> 杜鹃花科(Ericaceae)为中国植物的第七大科。因此,它在中国植物地理是中国植物区系上都占有比较重要的地位。杜鹃花科共分五个亚科:杜鹃花亚科、綟木亚科,白珠树亚科、北极果亚科和乌饭树亚科。綟木亚科、白珠树亚科和北极果亚科,虽然在本科中其种类不算太多,但所含10个属,故其多样性在本科中是首屈一指的。无疑,对这三个亚科在中国的地理分布及其与其他地区的关系的讨论是有意义的。 相似文献
20.
楝科(Meliaceae)的地理分布 总被引:9,自引:0,他引:9
陈邦余 《热带亚热带植物学报》1995,3(3):12-22
楝科为泛热带分布科,全世界有51属,约550—600种,分布于旧世界热带地区有46属,热带美洲有8属.热带亚洲和热带非洲为楝科两大现代分布中心.中国楝科共15属,61种,占世界属总数的29%,种总数的10%。中国楝科的分布是在全球楝科分布区的边缘,主要分布于中国西南部及南部诸省,种类由西南向东南递减。中国楝科属的分布区类型可归为5类:1.热带亚洲、非洲和中南美洲间断分布(1属);2.旧世界热带分布(3属);3,热带亚洲至热带大洋洲分布(2属);4.热带亚洲至热带非洲分布(1属);5.热带亚洲分布(8属)。中国楝科种的分布区类型仅有2类:1.热带亚洲分布(31种);2.中国特有分布(30种)。楝科植物的起源推断在早白垩纪。中国楝科植物由印度—马来西亚成分及特有成分组成。热带亚洲的楝科植物主要是通过中南半岛和中国云南。广西和海南等地发生联系,而菲律宾和台湾之间可有直接的联系。 相似文献