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1.
从细胞色素b基因序列变异分析中国鲇形目鱼类的系统发育   总被引:18,自引:0,他引:18  
采用PCR技术获得中国鲇形目鱼类11科24属27个代表种类细胞色素b基因1138bp全序列,比较分析了来自北美洲、非洲的部分鲇形目鱼类同一基因序列,并选取脂鲤目、鲤形目和鲱形目鱼类作外类群,采用Bayesian方法和最大简约法(MP)构建分子系统树。结果表明:(1)鲇形目鱼类细胞色素b基因序列中,与脂鲤目、鲤形目以及鲱形目鱼类相比存在3bp的缺失;(2)鲇形目鱼类各科代表种类形成一单系群;(3)两种建树方法均支持铫科、粒鲇科和钝头鮠科形成一单系群;而胡子鲇科、刀鲇科、海鲇科、鮰科、长臀鮠科、鲢科、鲇科、棘脂鲿科、鲿科形成一大的单系群;但鳗鲇科的系统位置两种建树方法没有取得一致结果;而其中长臀鲍科与北美的鮰科形成姐妹群,胡子鲇、鮰科、鲇科、鲿科和鮡科是较明显的单系群。  相似文献   

2.
利用18S和ITS序列揭示8种鲇形目鱼类的系统发育   总被引:5,自引:0,他引:5  
为了探讨鲇形目(Siluriformes)鱼类系统发育关系,本研究克隆了黄颡鱼(Pelteobagrus fulvidraco)、长吻(Leiocassis longirostris)、斑鳠(Mystus guttatus)、革胡子鲇(Clarias gariepinus)、鲇鱼(Silurus asotus)和斑点叉尾(Ictalurus punctatus)6种鱼类的18S和两个内转录间隔区(包括全长ITS1-5.8S-ITS2)基因,结合GenBank中双须缺鳍鲇(Kryptopterus bicirrhis)和脂鳍胡鲇(Dinotopterus cunningtoni)的同源序列进行比较分析,结果表明,(1)8种鱼18S的长度为1814~1842bp,同源性达97%以上,5.8S均为157bp,同源性也高达99.36%~100%;(2)8种鱼ITS1长度为335~620bp,其中,黄颡鱼的最长,为618~620bp,斑点叉尾的最短,为335~336bp;ITS2长度为265~459bp,其中,脂鳍胡鲇最长,为459bp,斑点叉尾的最短,约为270bp。ITS1序列的同源性为29.45%~88.21%,其中,革胡子鲇和脂鳍胡鲇同源性最高,鲇鱼和革胡子鲇同源性最低。ITS2序列的同源性为41.59%~94.07%,其中,革胡子鲇和脂鳍胡鲇同源性最高,鲇鱼和革胡子鲇同源性最低;(3)分别以鲤鱼(Cyprinus carpio)18S和ITS为外群,采用NJ法构建18S、ITS系统发育树,结果显示,鲇科与胡鲇科的关系最近,鲿科与这两科关系较远,科与另外3科关系最远。鲿科中属和黄颡鱼属的关系较鳠属更近;胡鲇科的胡鲇属和脂鳍胡鲇属是关系很近的两个属;鲇科的鲇属和缺鳍鲇属是关系较远的两属。  相似文献   

3.
国内外学者对硬骨鱼类的GH的季节变动及神经内分泌调控有一定的研究,其中在鲤科和鲑鳟鱼类研究的较为深入,近来一些学者对鲇形目的胡子鲇科、(鱼危)科[1]和鲇科[2]做了一定的研究,研究结果表明,GH分泌和神经内分泌调节机理与鲤科鱼类在某些方面存在一定差异.  相似文献   

4.
长臀鮠生长激素的生殖周期变化   总被引:1,自引:0,他引:1  
国内外学者对硬骨鱼类的GH的季节变动及神经内分泌调控有一定的研究,其中在鲤科和鲑鳟鱼类研究的较为深入,近来一些学者对鲇形目的胡子鲇科、科和鲇科做了一定的研究,研究结果表明,GH分泌和神经内分泌调节机理与鲤科鱼类在某些方面存在一定差异。如鲤科鱼类中,GnRH起着GH释放因子的作用,但非洲鲇鱼和鲇鱼中却未证实GnRH刺激GH释放,并且鲇鱼中GH分泌的季节变化与生殖之间有密切联系。    相似文献   

5.
与高等脊椎动物相比,鱼类的性别决定和生殖方式纷繁多样。环境因子、遗传等多种因素均可调控鱼类的性腺发生和分化[1,2],并对其生长、繁殖等重要生命活动产生影响。胡子鲇(Clarias fuscus)又称塘虱鱼,属鲇形目(Siluriformes)、胡子鲇科(Clariidae)、胡子鲇属(Clarias),  相似文献   

6.
中国鲿科鱼类线粒体DNA控制区结构及其系统发育分析   总被引:40,自引:4,他引:36  
采用PCR技术获得了中国鲿科鱼类代表种类线粒体DNA控制区基因的全序列,对控制区基因结构进行了分析,并选用粒鲇科的中华粒鲇,鮡科的三线纹胸鮡作为外类群,用最大简约法(MP)和邻接法(NJ)构建了系统发育树。结果显示鲿科鱼类中控制区基因适于系统发育分析,鲿科鱼类构成一个单系类群;圆尾拟鲿应该放入鮠属里。  相似文献   

7.
锡伯鲇科Schilbeidae的刀鲇属Platytropius Hora鱼类分布于我国云南省南部和泰国南部的江河中,我国有二种,均为以往文献中所没有记载过的新种。全部模式标本保存于中国科学院昆明动物研究所。 中华刀鲇Platytropius sinensis,新种(图1—4) 地方名:绸子鱼(西双版纳,云县,澜沧县和双江县),Bazhelang(西双版纳傣语)。  相似文献   

8.
粒鲇科Akyisidae鱼类是分布在东南亚地区的小型鱼类,包括三个属。其中大粒鲇属Achrochodomchthys Bleeker只产于苏门答腊岛、爪哇岛和加里曼丹岛。狭尾粒鲇属Breitensteinia Steindachner只产于苏门答腊岛和加里曼丹岛。粒鲇属Akysis Bleeker鱼类已记录的有下列8种:Akysis variegatus(Bleeker),1846;Akysis macronemus Bleeker,1860;Akysis pictus Gnther,1883;Akysis armatus Vaillant,1902;Akysis leucorhynchus Fowler,1934;Akysis maculipinnis Fowler,1934;Akysisprashadi Hora,1936;Akysis hendricksoni Alfred,1966.它们分布于缅甸、泰国、马来西亚和印度尼西亚等地。  相似文献   

9.
黄颡鱼与长须黄颡鱼种间的RAPD标记   总被引:5,自引:0,他引:5  
黄颡鱼属(Pelteobagrus Bleeker, 1865-属鲇形目( Siluri formes), 科(Bagridae-。    相似文献   

10.
瓦氏黄颡鱼线粒体全基因组序列分析及系统进化   总被引:3,自引:0,他引:3  
鲿科鱼类种类繁多, 外形相似, 形态学分类较为困难。为了给鲿科鱼类乃至鲇形目鱼类的系统进化研究积累基础资料, 文章采用参照近缘物种线粒体基因组设计覆盖全基因组引物的方法, 利用16对引物对瓦氏黄颡鱼(Pelteobagrus vachelli)线粒体全基因组进行扩增, PCR产物转化到质粒后测序, 最终获得线粒体基因组全序列, 其全长为16 527 bp, 包括2个rRNA基因、22个tRNA基因、13个编码蛋白质基因和一个非编码控制区。瓦氏黄颡鱼(P. vachelli)线粒体基因组结构和基因排列顺序与现已公布的鲇形目鱼类完全一致, 序列分析表明, 与鲇形目其他种属间具有较高的同源性, 与拟鲿属的同源性最高(91%)。利用鲇形目共4科6属9种及3个外群的线粒体全基因组序列, 从线粒体基因组水平探讨了鲿科鱼类及其在鲇形目的系统进化地位, 结果表明: 鲿科鱼类的瓦氏黄颡鱼(P. vachelli)、黄颡鱼(Pelteobagrus fulvidraco)、光泽黄颡鱼(Pelteobagrus nitidus)及越南拟鲿(Pseudobagrus tokiensis)构成一单系群; 拟鲿属与黄颡鱼属的关系较近; 黄颡鱼属中瓦氏黄颡鱼(P. vachelli)与光泽黄颡鱼(P.nitidus)的关系近于黄颡鱼(P. fulvidraco)。  相似文献   

11.
分析了斑叶蝉族昆虫在中国以及贵州动物地理区的分布情况,探讨其分布格局形成、起源和演化原因。根据中国和贵州斑叶蝉族的地理分布数据,运用MEGA 6.0、SPSS 22.0和ArcGIS 10.2等软件,对斑叶蝉族昆虫的区及亚区分布进行支序聚类分析,结果表明我国斑叶蝉族现代分布中心为西部山地高原亚区、华南区的台湾亚区及滇南山地亚区,分布热点地区为西双版纳地区、海南地区和台湾地区。贵州斑叶蝉现代分布中心为黔东低山丘陵省、黔北中山峡谷省和黔南低山河谷省,分布热点地区为铜仁北部的沿河地区、遵义的务川地区及贵州黔东南州的榕江、雷山地区。斑叶蝉族昆虫中国分布区形成的顺序先是东北区,其次是青藏区和蒙新区,最后是西南区、华北区、华南区和华中区。贵州分布区形成的顺序先是黔西高原中山省和黔中山原丘陵省,其次是黔南低山河谷省,最后是黔北中山峡谷省和黔东低山丘陵省。中国分布区中,B21和B22聚类群属级阶元的相似性最高,区间关联性最强。在贵州分布区中黔东低山丘陵省和黔北中山峡谷省属级阶元的相似性最高,物种交流最为频繁。目前,斑叶蝉族昆虫的地理分布格局主要是历史气候变化、当前气候条件以及植被覆盖等生态环境共同作用的结果;区系起源和演化主要受地质构造运动作用;斑叶蝉在各区的分布相似性可能与气候变化引起的物种由南向北扩散有关。  相似文献   

12.
以中国动物地理亚区统计了1976年郑作新出版的《中国鸟类分布名录》和2005年郑光美主编出版的《中国鸟类分类与分布名录》中繁殖鸟类的分布数据,结果显示:在1976年前,中国鸟类丰富度最高的动物地理亚区为西南山地亚区,其次为滇南山地亚区,而以羌塘高原亚区鸟类物种丰富度最低,黄淮平原亚区次差。2005年,鸟类丰富度最高、次高及最低的亚区与1976年相同,次差的亚区为台湾亚区。自1976年至2005年,鸟类物种丰富度在不同亚区出现明显的增加,平均每个亚区分布物种数由1976年的232种增至2005年的281种,而且具有很大的相关性;其中滇南山地亚区增加种类最多,而羌塘高原亚区和东部草原亚区增加的幅度最大;在海南岛和台湾亚区则变化较小。这些可能是由于物种在不同亚区间存在的可能扩散通道和岛屿型稳定气候及地理隔离限制了物种与其它亚区间的扩散等造成的。这些变化不仅与Leietal.(2007)提出的"地理隔离"假设结论比较一致,与雷富民等(2006)提出的西南山地-横断山区为中国鸟类特有种物种多样性中心和西南山地为物种分化中心等观点一致,而且进一步显示西南山地亚区鸟类物种有向滇南山地亚区扩散的现象,并且依然在持续中。用聚类...  相似文献   

13.
中国画眉科鸟类分布格局探讨   总被引:3,自引:1,他引:3  
中国现有画眉科鸟类122种,隶属于27属,占我国鸟类总种数的9.15%。通过运用GIS技术处理物种分布数据,研究了中国画眉科鸟类的分布格局和多样性中心。中国画眉科鸟类在水平分布上具有不均匀性,省际单元上云南最多(102种),占绝对优势;在动物地理亚区单元上滇南山地亚区分布最多(80种),其次是西南山地亚区(60种)、喜马拉雅亚区(47种);在垂直分布上,则以700~2700m的海拔地带具有最高的物种多样性。中国画眉科鸟类物种多样性最高的地区位于滇南山地亚区与西南山地亚区的交汇地带—横断山区南端。我国画眉科鸟类主要涉及以下3个分布型:东洋型、喜马拉雅-横断山型和南中国型。  相似文献   

14.
宁夏哺乳动物区系与地理区划研究   总被引:10,自引:0,他引:10  
张显理  于有志 《兽类学报》1995,15(2):128-136
宁夏现有哺乳动物75种,隶属于6目19科52属 。本文分析了宁夏哺乳动物区系特征,将宁夏划分为3个动物地理省、6十动物地理州,并对各省及各州动物区系之间的相似性等问题进行了探讨。  相似文献   

15.
The Hengduan Mountain Region on the south-eastern fringe of the Qinghai- Xizang (Tibet) Plateau is located in W. Sichuan, N. W. Yunnan and E. Xizang, with a wide area of juxtaposition from the east to the west, the mountains extending and the rivers flowing from the north to the south. In this paper it covers an area from Daojie, Wayao, Yingping, Yangbi, Dali of Yunnan and Dukou of Sichuan in the south, to Banbar, Dengqeu, Shenda of Tibet and Serxu, Dainkog, Shuajingsi and Nanping (Jiuzhaigou) of Sichuan in the north, and from Lharong, Baxoi and Zayü of Tibet in the west, to Maowen, Wenchuan, Mt. Erlang, Mt. Emei and Xichang of Sichuan in the east (Fig. 1.). The Gongga Mountain is the highest in the region, its summit being at an altitude of 7556m, whereas the Dadu River Valley in the eastern part of the area is only 1150 m above sea level. Therefore, the relative height is about 6400 m in the region. The Hengduan Mountain Region is well-known for its various topography, complex natural conditions and rich flora. The floristic composition and features of orchids in Hengduan Mountain Region. 1. The species of orchids are abundant in the region. As we know so far, orchids in the Hengduan Mountain Region comprise 91 genera and 363 species with 9 varieties, and thus it is one of concentration centres of orchids in China, making up 56.17% of the total number of orchids genera in China, only less than in Yunnan and Taiwan, and 34.87% of the total number of orchids species in China, only less than in Yunnan and Sichuan. 2. The orchids genera in the Hengduan Mountain Region are complex in geographical components as indicated below: (1) Four geneva are endemic to China and one of them is endemic to the region. (2) Fourteen genera are of the north temperate distribution pattern, 2 of the Old World temperate one, 18 of the East-Asian one (including Sino-Himalayan and Sino-Japanese) and 3 of the East-Asian-North American one. (3) Twenty one genera belong to the tropical Asian distribution pattern, 3 to the tropical Asian-tropical African one, 13 to the tropical Asian-tropical Australian one, 1 to the tropical Asian-tropical South American one, 8 to the Old World tropical one and 2 to the pantropical one. (4) Two genera are cosmopolitan. The analysis of genera: Fourty eight genera (containing 151 species with 4 varieties) of the tropical distribution occur in the region, among which Calanthe and Cymbidium distributed in the temperate region, and Bulbophyllum and Peristylus in the subtropical part of China are comparatively abundant (with over 10 species), but the other 25 genera are monospecific and 11 genera each contain only 2-3 species. Some epiphytic genera mainly distributed in tropical Asia and belonging to tropical florestic elements, such as Vanda, Luisia, Schoenorchis, Flickingeria, Monomeria, Kingidium, Acampe, Phalaenopsis, Thrixspermum, Eria, Taeniophyllum, and terrestrial genera, such as Aphyllorchis, Collabium, Mischobulbum, Paphiopedilum, Thunia, Brachycarythis, Satyrium, Corybas, Geodorum, Zeuxine, Tropidia, have the Hengduan Mountain Region as the northern limit of distribution. Of 151 species with 4 varieties, 41 species with 4 varieties are endemic to China, and 14 species with 3 varieties of them are endemic to the area, making up 3.86% of the total in the region under discussion. There are 41 genera (containing 189 species with 5 varieties) of the temperate distribution, which occur in the region. Among them Platanthera (22 species with 1 variety), Cypripedium (17 species), Herminium (16 species), Amitostigma (15 species with 1 variety), Orchis (12 species), Hemipilia (8 species with 1 variety), Neottianthe (4 species), Gymnadenia (4 species), Diphylax (3 species), Bletilla (3 species), have the Hengduan Mountain Region as the distribution centre and differentiation centre. Among the 189 species with 5 varieties, 111 species with 5 varieties are endemic to China, and 54 species with 5 varieties are endemic to the area, making up 14.88% of the total of orchids in the Hengduan Mountain Region. Although the number of temperate distribution genera is smaller than that of tropical distribution ones, several points may be mentioned: (1) The Hengduan Mountain Region is distribution centre and differentiation centre of a number of temperate genera in China, and is the northern limit of many genera mainly distributed in the tropics. (2) The number in the former category is obviously larger than that in the latter. (3) Endemic species in the former category in the area are over three times as many as those in the latter. The differentiation of species of the temperate distribution genera is obviously stronger than the tropical ones, which characterizes the orchid flora in the area as the temperate one. The life forms of genera. The orchid flora in the Hengduan Mountain Region so far known comprises 91 genera, among which 51 are terrestrial, 32 epiphytic and 8 saprophytic, thus with the terrestrial one dominant. The analysis of species: The orchid flora in the Hengduan Mountain Region so far known comprises 363 species with 9 varieties. Their distribution patterns and floristic components, to which they belong, are indicated as follows: (1) Fifty four species, belonging to 33 genera, are widespread, covering the whole East Asian Region, but 6 of them are endemic to China. (2) Forty four species, belonging to 27 genera, are the elements of the Sino-Japanese Subregion, but 22 species of them are endemic to China. (3) One hundred and ninety five species with nine varieties, belonging to 53 genera, are the elements of the Sino-Himalayan Subregion under discussion: (A) Four species (i.e. Aphyllorchis alpine, Listera divaricata, L. pinetorum and Oreorchis micrantha) are distributed in the Himalayan Region and S. E. Xizang (Tibet), western part of this region. (B) Twenty five species, belonging to 17 genera, are distributed in N. W. Yunnan and the Himalayan Region (Appendix, 1.). (C) Sixteen species, belonging to 11 genera, are distributed in the Himalayan region and W. Sichuan. Among them 6 species occur only with Mt. Emei as the easternmost limit and 10 species occur in the region west of Mt. Emei. (D) Ten species, belonging to 9 genera, are distributed in the Himalayan region, this region and S. Shaanxi, S. Gansu or S. E. Qinghai. (E) Eight species, belonging to 6 genera, are distributed in the Himalayan region and this region. Among them 6 species have their range extending eastwards to Guizhou and 2 species eastwards to Guangxi. (F) Five species, belonging to 5 genera, having their range extending from this region southwards to N. Burma. (G) One handred and twenty seven species with nine varieties are endemic to China behind discussion. (4) (A) Three species (i.e. Anoectochilus moulmeinensis, Bulbophyllum forrestii and Liparis chapaensis) are distributed in Indo-China, Burma and the region. (B) Nine species, belonging to 7 genera, are distributed in Indo-China, N. E. India and this region. (C) Forty six species, belonging to 21 genera, are distributed in Indo-China, the Himalayan Region and this region (Appendix, 2.). (D) Twelve species, belonging to 11 genera, are distributed in Indo-China and this region (Appendix, 3.) 3. The vicarism is obvious in the orchid flora of the Hengduan Mountain Region. There are 10 species-pairs (in genera Calanthe, Tropidia, Anoectochilus, Mischobulbum, Bulbophyllum, Gymnadenia, Pogonia, Tipularia, Tulotis, Orchis, etc.) of the horizontal vicarism and 7 species-pairs (in genera Epigeneium, Epipogium, Platanthera, Pogonia, etc.) of the vertical vicarism in the region. 4. The endemic species are prolific in the region. In the orchid flora of the Hengduan Mountain Region there are 155 species and 9 varieties endemic to China: (1) Six species are widespread in the whole East-Asian Region. (2) Twenty two species are the elements of the Sino-Japanese Subregion. (3) One hundred and twenty seven species with nine varieties are the elements of the Sino-Himalayan Subregion. Among them 69 species with 5 varieties are endemic to the region (Appendix, 4.), making up 19% of the total in the region; other 58 species with 4 varieties are distributed in the region and neighbouring regions or provinces of it (Appendix, 5.). 5. Remarkable differentiation of the orchid flora in the Hengduan Mountain Region is shown by evident vicarism and abundance of endemic elements, exampled by Amitostigma, Herminium, Orchis, Cypripedium, Platanthera, etc. and one group of Platanthera, which is confined to the south fringe of the Xizang (Tibet) Plateau-Hengduan Mountain Region. The group consists of 12 species, of which one (P. edgeworthii) is distributed in the Western Himalayas from Hazara in Pakistan to Kumaun in India, and all the other 11 species (i.e.P. stenantha, P. bakeriana, P. roseotincta, P. deflexilabella, P. longiglandula, P. exilliana, P. chiloglossa, P. leptocaulon, P. platantheroides, P. clavigera and P. latilabris) occur in China, with 3 of them (i.e.P. deflexilabella, P. longiglandula and P. chiloglossa) endemic to China. According to their structure of gynostemum and form of labellum they belong to Platanthera without question, although they are different from the other members of Platanthera in stigma convex (not concave) and sepals mammillary-ciliate, stigma exhibits a series of evolutionary trends in part of species, from stigma single, convex, elliptic and located near rear of spur mouth (in P. stenantha) to stigma single, suddle, and located near front of spur mouth (in P. bakeriana) and to stigma double, separate and located at front of spur mouth in the other ten species. The group in Platanthera is only confined to the area from the south fringe of the Xizang (Tibet) Plateau to the Hengduan Mountain Region. It seems that the genus has been affected by intense lift of the area, causing variation and differentiation and giving rise to the group due to the long-term natural selection. Mt. Emei in Sichuan Province is the eastern limit of distribution of the group, where there are three spcies, among which two (P. deflexilabella and P. longiglandula) are endemic to the mountains. In addition, among Risleya (1 species), Diphylax (3 species) and Diplomeris (2 species), three genera typical of distribution in the Sino-Himalayan Subregion, Risleya and Diphylax have Mt. Emei as their eastern limit. Eleven species, belonging to elements of the SinoJapanese Subregion, occur only from Japan to Western Sichuan with Mt. Emei as the western limit. Among nine species, belonging to elements of the Sino-Himalayan Subregion, six occur from the Himalayas to W. Sichuan and three of them are endemic to the Hengduan Mountain Region, with Mt. Emei as their eastern limit of distribution. There are eight endemic species and one variety of orchids in Mt. Emei, making up about 11.59% of the total endemic species in the Hengduan Mountain Region. Orchid floristic elements in Mt. Emei are obviously different from those in Mt. Jinfo, the former being mainly of the Sino-Himalayan Subregion, while the latter being mainly of the Sino-Japanese Subregion. From the distribution patterns of the orchid floristic elements in the Hengduan Mountain Region and Eastern China, the Emei Mountain is considered important for drawing a boundary line between the Sino-Japanese Subregion and the Sino-Himalayan Subregion. The discussion may be summarized as follows: the floristic features of the orchid flora in the Hengduan Mountain Region are: (1) rich in species, complex in geographical components, eminent vicarism and differentiation, and prolific in endemic species; (2) terrestrial life form is dominant one; (3) mainly consisting of temperate and subtropical East-Asian elements, es pecially, elements of Sino-Himalayan Subregion, though with some tropical elements and elem-ents of other regions.  相似文献   

16.
中国夜蛾科昆虫的物种多样性及分布格局   总被引:5,自引:0,他引:5  
申效诚  孙浩  赵华东 《昆虫学报》2007,50(7):709-719
本文在收集整理中国夜蛾全部种类名录和分布资料的数据库基础上,对其分布格局进行了分析。结果表明:中国夜蛾共有20个亚科845个有效属3 751个有效种,占世界种类的13.66%,其中1 734种模式产地在中国。这些种类主要归属4种区系成分,其中东亚成分占优势,占总数的51.35%,东洋成分占25.51%,古北成分占18.45%,广布成分仅2.26%。夜蛾在全国七个动物地理区中的分布,是不同类群不同分布特点的复合体,84种广布种分布广泛而均匀,七区之间的多元相似性系数达显著水平。 957种东洋种类和692种古北种类随纬度呈阶梯状分布,各区间无显著相似性。 1 926种东亚种类中,南中国型1 363种,分别较为孤立地分布在华南、华中、西南三区,各区之间联系微弱; 北中国型290种,零星分散地分布在东北、蒙新、华北、青藏四区; 中中国型273种遍布全国,但主要分布在我国中部的华北、华中、西南、青藏四区,以跨界分布为特点,四区之间具有显著的多元相似性。特有种的简约性分析结果表明,特有分布区的分布和划分基本和中国动物地理区划相一致,但台湾和华中区关系密切。关键区系分析显示,台湾、云南、新疆、西藏等11个省区包含了中国夜蛾物种的90%,是物种保护的优先区域。  相似文献   

17.
Aim  To provide an objective geographic framework displaying the distribution patterns of freshwater fishes from Argentina.
Location  Argentina, southern South America.
Methods  Parsimony analysis of endemicity (PAE) and similarity and cluster analyses were applied to presence and absence data on 440 fish species from 52 localities in Argentina. Both 50% majority consensus and strict consensus analyses were undertaken in the first case, and the Jaccard similarity index was used in the second.
Results  Five ichthyogeographic provinces are described based on a PAE of the 52 localities. A cluster analysis provided similar results.
Main conclusions  The following zoogeographic provinces are proposed for Argentine freshwater fish fauna following the International Code of Area Nomenclature: Andean Cuyan, Patagonian, Aymaran, Great Rivers and Pampean. The former two are placed within the Andean Subregion of the Austral Region, and the latter three within the Neotropical Subregion of the Holotropical Region. These provinces, based on results coinciding with PAE and cluster analysis, represent the first classification of Argentine provinces based on objective methods. Some small regions of endemism and some localities remain separated from the proposed regions. The new scheme includes valuable empirical information from previous schemes, and is in agreement with ecological zones and other environmental arrangements proposed earlier.  相似文献   

18.
西北地区木本植物区系多样性研究   总被引:15,自引:0,他引:15  
西北地区在中国植物区系上属于泛北极植物区,其南部基本上控制在中国-日本植物亚区的华中地区内,区系成分以北亚热带成分占优势,中、东部主要控制在中国-日本植物亚区内的华北地区中的黄土高原地区内,以华北区系成分占优势,西南部主要属青藏高原植物亚区和中国-喜马拉雅植物亚区,区系成分以唐古特和横断山区系成分占优势,北部主要是亚洲荒漠植物亚区,区系成分是以古地中海成分占优势。本区有木本植物(不包括栽培植物)103科338属1729种(含种下等级),其中裸子植物6科17属57种,被子植物97科321属1672种,另外,具有中国特有属26个,土著特有种173个(含种下等级)。大科、大属在区系组成中起着非常重要的作用,该区木本植物区系包含有15个分布区类型及其17个变型,其中北温带分布、泛热带分布、东亚至北美间断分布、东亚分布等成分占有重要地位。其木本植物区系的主要特征为:种类比较丰富;分布不均,区域差异大;地理成分复杂,具有明显的温带性质;起源古老;土著特有种较多;区系联系广泛,多种区系成分的汇集、混杂和过渡。  相似文献   

19.
云南蚤类区系及分布特征   总被引:5,自引:0,他引:5  
【目的】在收集汇总以往野外调查资料以及已经发表的历史文献资料基础上,归纳云南蚤类的分布特点,分析云南地理小区对蚤类的影响。【方法】在实地采集和补充文献记录基础上,对收集到的蚤类进行系统分类整理;运用SPSS13.0的主成分分析及系统聚类对数据进行处理。【结果】本研究共记录云南蚤类9科45属144种,其中古北种15种,东洋种 108种,东洋、古北两界兼有种15种,广布种6种。144种蚤中,属于云南特有蚤类有75种;横断山中部小区记载蚤类122种,横断山南部小区26种,滇东高原小区41种,滇西高原小区28种,滇南山地小区25种。主成分分析和聚类分析结果基本一致,均可聚为两类:一类为横断山南部小区、滇南山地小区、滇西高原小区及滇东高原小区; 另一类为横断山中部小区。【结论】云南省蚤类分布明显受到地理小区环境的影响。云南省蚤类昆虫种类繁多,蚤类的自然分布受到云南省特定地形地貌影响。  相似文献   

20.
分析了中国蛱蝶科已知324种昆虫的分布与区系组成,主要由古北区、东洋区、古北一东洋区共有种类组成,共计309种,占总数的95.37%;其种类组成与澳洲区、新北区有明显差异;特有种类较少,占总数的12.65%;广布种很少,仅占1.74%。同时统计分析了324种蛱蝶在我国各省的贫富指数。  相似文献   

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